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conceptofmind
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minipile_embeddings_bf16

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/** * This demonstrates how the Java volatile type qualifier can be used * to enable two threads to alternate printing "ping" and "pong." * Additional information about this technique appears at URL * https://dzone.com/articles/java-volatile-keyword-0. */ public class ex31 { /** * Sleep for {@code milliseconds}. */ private static void sleep(int milliseconds) { try { Thread.sleep(milliseconds); } catch (InterruptedException e) { e.printStackTrace(); } } /** * Print out parameter {@code s} prefixed with thread info. */ private static void print(String s) { System.out.println(Thread.currentThread() + ": " + s); } /** * Demonstrates how the Java volatile type qualifier can * be used to coordinate behavior between two threads that * alternatve printing "ping" and "pong". */ static class PingPongTest { /** * The volatile value that's shared between threads. */ private volatile int mVal = 0; /** * Max number of iterations. */ private int sMAX_ITERATIONS = 5; /** * Create/start two threads that alternate printing * "ping" and "pong". */ public void playPingPong() { // Create a new thread "pong" thread whose // runnable lambda listens for changes to mVal; new Thread(() -> { for (int lv = mVal; lv < sMAX_ITERATIONS; ) // Only do the body of the if statement when // lv changes. if (lv != mVal) { print("pong(" + mVal + ")"); // Read lv from volatile mVal. lv = mVal; } }).start(); // Create a new "ping" thread whose runnable lambda // changes the value of mVal on each loop iteration. new Thread(() -> { for (int lv = mVal; mVal < sMAX_ITERATIONS; ) { print("ping(" + ++lv + ")"); // Set volatile mVal to next value of lv. mVal = lv; sleep(500); } }).start(); } } /** * The Java execution environment requires a static main() entry * point method to run the app. */ public static void main(String[] args) { // Run the test program. new PingPongTest().playPingPong(); } }
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1. Field of the Invention The invention relates to devices for making soap bubbles. 2. Description of the Related Art Children are fascinated with the production of soap bubbles. For this reason, numerous types of bubble toy machines have been developed. Perhaps the oldest and simplest is the wire or plastic frame which is dipped into bubble making liquid, such as liquid dish washing soap, and bubbles are then blown from the wire. In recent years, more elaborate toys have been developed using the same basic theory. These toys are designed for the user to blow on part of the apparatus to produce bubbles. The disadvantage with this technique is that the user must place their mouth on or about the apparatus. This is a problem, particularly when there are many users operating the apparatus, thus promoting the spread of germs among children. There have been toys developed over the years which do not necessitate the user operating the apparatus by blowing on it. However, most of these devices are complex and therefore expensive to produce. Most of these devices produce bubbles by blowing air through bubble solution. Representative of the genre is U.S. Pat. No. 4,347,682. The patent is a bubble toy operated by manually blowing through an opening in the center of the toy. The air is blown through a cap on the end of the toy. This cap is emerged in the bubble solution, and as the air enters the cap, soap bubbles are formed. Another bubble toy is represented by U.S. Pat. No. 4,044,496. This toy is activated by rotating a gear crank, which turns a propeller. This toy is not designed to submerge into water and bubble solution, but rather the solution is introduced into a resevoir within the toy itself. Another bubble toy is represented by U.S. Pat. No. 3,708,909. This toy utilizes a disk with apertures. However, this toy is operated by pneumatic force rather than manual operation. The prior art does not show a safe bubble producing toy that can be used successfully by a child in a bathtub or other clear or soapy water area, that is unique in the manner of bubble production, and that is capable of reusing the bubble solution. In addition, the prior art does not show a bubble producing toy that utilizes water, air and bubble solution as opposed to only air and bubble solution.
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The accurate identification of a specific microbial pathogen is crucial in many infectious disease syndromes as it facilitates a clear diagnosis, allows for targeted therapy, and increases the likelihood of a favorable outcome \[[@CIT0001], [@CIT0002]\] However, using culture-based diagnostic methods, organisms cannot always be isolated, either due to their fastidious nature or the use of empiric antimicrobials before specimen collection \[[@CIT0003]\]. Molecular diagnostics based on nucleic acid target amplification and sequencing technology (also known as "broad-range" polymerase chain reaction \[PCR\]) are increasingly used for investigation of culture-negative infections. These tests are able to accurately identify microorganisms based on specific regions such as 16S rRNA (for identification of bacteria), rpoB (for mycobacteria), or the internal transcribed spacer region (fungi) and have been used in clinical microbiology for more than 2 decades \[[@CIT0007]\]. These techniques were initially applied to microbial isolates that could not be definitively identified by phenotypic means, and they perform well in this scenario \[[@CIT0008]\]. More recently, they have been increasingly used directly on clinical tissue/fluid samples aiming to identify fastidious organisms that are difficult to culture, or in patients who have been exposed to antimicrobials before specimen collection. In this situation, sensitivity may be lower and methodology more complex due to the tissue extraction process required, potential inhibitors present, and increased likelihood of contamination leading to false-positive results \[[@CIT0009]\]. In 1 large study using 16S rRNA PCR, Rampini et al. demonstrated 91% concordance with bacterial cultures in 394 culture-positive samples and were able to identify 24 bacteria among 184 culture-negative samples \[[@CIT0010]\]. 16S rRNA PCR is also increasingly being used as part of the diagnostic evaluation of prosthetic joint infection \[[@CIT0011]\] and culture-negative endocarditis \[[@CIT0011], [@CIT0014]\]. Given the high cost, technical complexity, and time required to perform these tests, attempts have been made in many institutions to try and target their use toward patients most likely to benefit, aiming to optimize test performance and cost-effectiveness. This has included considering factors such as clinical features, serum inflammatory markers, and evidence of infection on microbiologic or histopathologic stains and culture results. Several studies have explored the relationships between these variables and bacteriologic culture results \[[@CIT0017]\]. One small study identified a positive association between serum C-reactive protein (CRP) and tissue neutrophil count and level of bacterial DNA measured by cycle threshold \[[@CIT0020]\], but in general the relationships between clinical features and broad-range PCR results are not well studied. In most prior studies, broad-range PCR has been directly compared with culture-based diagnostic methods, despite the fact that increasingly in modern clinical practice it is being used when cultures are negative \[[@CIT0012], [@CIT0021]\]. Additionally, few studies have examined the overall clinical utility and impact of this test on patient management \[[@CIT0021], [@CIT0026]\]. The aim of this retrospective cohort study was to assess the real-world clinical performance of broad-range PCR at our institution using a "composite clinical gold standard" and determine its impact on antimicrobial decision-making. We also evaluated clinical factors such as pathological findings and presence of polymorphonuclear leukocytes associated with a positive PCR result to guide selection of specimens appropriate for PCR testing. METHODS {#s1} ======= Study Design and Data Collection {#s2} -------------------------------- The study population consisted of patients at Tufts Medical Center, a 415-bed academic medical center in Boston, Massachusetts, whose tissue and fluid samples were sent for broad-range PCR testing from August 2013 to April 2016, excluding those lost to follow-up (defined as lack of inpatient/outpatient documentation in medical records after the broad-range PCR was performed). The study was approved by the Tufts Medical Center institutional review board; informed consent was not required given the minimal risk and retrospective nature of the study. Clinical data were collected from medical records. All cases were reviewed by a panel of 3 infectious diseases physicians blinded to PCR results but provided with all other relevant clinical information. The panel determined the presence or absence of infection by using a final gold standard of "composite clinical diagnosis" based on all available data, including medical history, clinical signs and symptoms, operative findings, laboratory testing results including inflammatory markers (C-reactive protein and erythrocyte sedimentation rate), Gram stain results, histopathologic findings, microbiologic, serologic, and radiologic data, and prior antibiotic therapy. Final classification in cases of disagreement was by majority opinion. Specimen Collection and Laboratory Methods {#s3} ------------------------------------------ The majority of samples were collected under sterile conditions in the operating room or interventional radiology suite, divided at the point of collection, and then sent separately for histopathology and microbiology testing. Occasionally, undivided samples were sent, and these were processed first in the microbiology laboratory then sent to histopathology to avoid contamination. Gram stains (including quantification of bacteria and blood cells) and cultures of tissue specimens were performed in the clinical microbiology laboratory at Tufts Medical Center according to CLSI standards \[[@CIT0029]\]. Tissue specimens were examined for the presence of polymorphonuclear leukocytes (PMNs) and reported in a semiquantitative fashion on a scale of 0--4, corresponding to \<1, 1, 2--10, 11--25, and \>25 cells per low power field, respectively. For the purposes of analysis, specimens were considered to have a "high" number of leucocytes if they had ≥11 cells per low power field, or ≥3 on this scale. This definition was adapted from prior published studies of prosthetic joint infection and modified to suit our patient population and local diagnostic testing criteria \[[@CIT0029]\]. The presence of organisms was recorded based on the number per high power field on a similar scale. Samples were also typically submitted for bacterial, mycobacterial, and fungal cultures. Pathological examination of tissue specimens was performed in the Pathology Laboratory at Tufts Medical Center, and samples were considered to have evidence of infection if there was infiltration with neutrophils, macrophages, or other inflammatory cells, or caseating granulomatous inflammation was seen \[[@CIT0034]\]. PCR testing was performed at the University of Washington Molecular Diagnostic Laboratory, with samples sent for bacterial, fungal, and/or mycobacterial testing using methods previously described \[[@CIT0012], [@CIT0022], [@CIT0035]\]. Broad-range bacterial PCR targeted the 16S rRNA (forward primer 27F sequence, 5'-AGAGTTTGATCCTGGCTCAG-3'; reverse primer 357-mL sequence, 5'-CTGCTGCCICCCGTAGGAG-3') \[[@CIT0035]\]. Mycobacterial PCR utilized 3 targets including hsp65 (TB11, 5'-ACCAACGATGGTGTGTCCAT-3'; TB12, 5'-CTTGTCGAACCGCATACCCT-3') \[[@CIT0041]\], rpoB (MF, 5′-CGACCACTTCGGCAACCG-3′; MR, 5′-TCGATCGGGC ACATCCGG-3′) \[[@CIT0042]\], and 16S (as for bacteria). Fungal PCR also used 3 targets: 28S (NL1, 5′-GCATATCAA TAA GCGGAGGAAAAG-3′; NL4, 5′-GGTCCGTGTTT CAAGACGG-3′), ITS1 (ITS1, 5′-TCCGTAGGTGAACCTGC GG-3′; ITS2, 5′-GCATCGATGAAGAACGCAGC-3′), and ITS2 (ITS3, 5′-GCATCGATGAAGAACGCAGC-3′; ITS4, 5′-GCATATCAATAAGCGGAGGA-3′) \[[@CIT0043]\]. The decision regarding which PCRs to send (bacterial, fungal, and/or mycobacterial) and the timing was determined by the individual clinicians managing each case. Clinical Diagnosis of Infection, Diagnostic Accuracy, and Outcome Ascertainment {#s4} ------------------------------------------------------------------------------- As no uniform criteria have been established for the diagnosis of infection, clinical infection was considered based on the following criteria: (1) presence of clinical manifestations that reflect host damage in the setting of microbial infection such as fever and/or systemic symptoms and/or localizing symptoms of infections and (2) laboratory or radiographic parameters indicative of host damage such as leukocytosis, elevated inflammatory markers, and microbiological, histological, and/or radiological evidence of infection \[[@CIT0044]\]. The presence or absence of infection was defined using a gold standard composite clinical diagnosis based on the assessment of 3 independent infectious diseases physicians, as described above. Following this review, clinical classifications were aligned with PCR results to designate patients as true positive (PCR positive with clinical evidence of infection), false positive (PCR positive without clinical evidence of infection), true negative (PCR negative without clinical infection), or false negative (PCR negative with clinical infection). Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated. The impact of the test results on clinical decision-making was assessed by examining medical records for documentation regarding antimicrobial changes made after PCR results were available. This included any active optimization of antibiotic therapy such as de-escalation to a narrower-spectrum agent, the transition of patients from intravenous (IV) to oral antibiotics, changing to a different class of antimicrobials, or discontinuation of antimicrobial therapy altogether \[[@CIT0045]\]. Statistical Analysis {#s5} -------------------- Categorical data were reported as percentages, and continuous data were reported as means ± standard deviations if normally distributed and medians with ranges if non-normally distributed. Odds ratios were calculated, and variables were compared across PCR result status using univariate logistic regression. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated by comparing the broad-range PCR result with our composite final clinical diagnosis. RESULTS {#s6} ======= A total of 74 samples from 73 patients were sent for broad-range PCR testing during the study period. Three patients were excluded, 1 for whom no result was available and 2 who were lost to follow-up, leaving 71 samples from 70 patients in our final cohort ([Figure 1](#F1){ref-type="fig"}). Individual sample details are available in the [Supplementary Table](#sup1){ref-type="supplementary-material"}. Thirty-nine patients (55%) were male, and the mean age was 57.8 ± 15.6 years. There were 13 patients who either did not have samples sent to microbiology at all or did not have sufficient tissue left in microbiology, and as such PCR testing was performed on formalin-fixed, paraffin-embedded (FFPE) tissue. There were 21 tissue samples with positive broad-range PCR results and 50 with negative results, 35 from orthopedic sites and 36 from nonorthopedic sites ([Table 1](#T1){ref-type="table"}). Two samples were positive for more than 2 organisms. Thirteen bacteria, 3 mycobacteria, and 7 fungi were identified. Organisms were mostly unique, though some were identified more than once, including *Propionibacterium acnes* (n = 2), *Mycobacterium tuberculosis* (n = 2), and *Aspergillus* species (n = 2). Antibiotic use was common (42/71; 59%), with 37 patients actively receiving antibiotics at the time the specimens were obtained, for a median duration (interquartile range) of 15 (6--44) days. There was an array of agents, but they were typically broad spectrum. Four patients were receiving long-term antibiotics for at least several months. An additional 5 patients had received antibiotics within the 4 weeks before sampling. ![Diagram demonstrating number and flow of samples/patients included in the study. Abbreviation: PCR, polymerase chain reaction.](ofy25701){#F1} ###### Summary of Specimen Sites and Corresponding PCR Results ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Specimen Site\ No. of Samples Organisms Identified (n = 71) ------------------------------ ---------------- ---------------------------------------------------------------------------------------------------------------------------- Nonorthopedic sites (n = 36) Abdominal abscess 2 *Aspergillus fumigatus*/*Ureaplasma urealyticum*^a^ Bronchoalveolar lavage 1 *Cryptococcus neoformans* ^b^ Brain 1 Cerebrospinal fluid 3 *Fusobacterium nucleatum* ^b^ Epidural abscess 1 Eye 2 Heart valve 5 *Bartonella henselae*,^b^*Cunninghamella*,^b^*Streptococcus mitis*^b^ Liver 1 Lung 2 *Pneumocystis jirovecii* ^b^ Lymph node 2 Muscle 1 Myocardium 3 *Aspergillus species* ^b^ Pleural fluid 1 Psoas abscess 1 *Mycobacterium tuberculosis* ^b^ Sinus 2 *Rhizopus oryzae* ^b^ Spine 7 *Malassezia restricta*,^b^*Mycobacterium tuberculosis*,^b^*Propionibacterium acnes*^b^ Testis 1 Orthopedic sites (n = 35) Ankle 2 *Streptococcus agalactiae* ^b^ Hip 11 *Streptococcus pneumoniae*,^b^*Mycobacterium avium* complex^b^ Knee 15 *Staphylococcus epidermidis*,^b^*Streptococcus mitis*^b^ Phalanx 1 Tibia 4 *Propionibacterium acnes*,^b^*Pseudomonas aeruginosa*,^b^*Staphylococcus pettenkoferi/Staphylococcus pseudolugdunensis*^a^ Wrist 2 ---------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Abbreviation: PCR, polymerase chain reaction. ^a^Both organisms identified in the same sample. ^b^Isolated from a single specimen alone, with no other organisms. In deciding presence or absence of clinical infection, there was complete agreement in 58% of cases, and the remainders were by majority opinion. Thirty-seven patients (52%) were thought to have likely infection according to our composite clinical gold standard diagnosis. Of these, 19 had positive PCR results (true positives), and 18 had negative PCR results (false negatives). Of the 34 without clinical infection, 2 patients had positive PCR results (false positives), and 32 patients had negative PCR results (true negatives). This correlated to a sensitivity of 51%, specificity of 94%, PPV of 91%, and NPV of 64% ([Table 2](#T2){ref-type="table"}). Patients with false positives were also examined in more detail. One sample classified as false positive was *Malassezia restricta*, obtained from a computed tomography--guided biopsy of the spine and considered to represent a sample retrieval contaminant given the nature of the organism. The second false positive was an *Aspergillus* species from a routine myocardial biopsy of a heart transplant recipient. The patient was asymptomatic, but the sample was sent for PCR due to the presence of micro-abscesses seen on pathologic examination. After discussion with a fungal expert from the reference laboratory, it was considered an environmental or laboratory contaminant as the *Aspergillus* PCR was positive in only 1 out of the 2 runs, and the result was inconsistent with the clinical context. ###### Sensitivity, Specificity, Positive and Negative Predictive Values of Universal PCR as Compared With a Gold Standard of Composite Clinical Diagnosis Determined by a Panel of Infectious Diseases Physicians Infection Present Infection Absent -------------- --------------------- -------------------- ----------- PCR positive 19 (true positive) 2 (false positive) PPV = 91% PCR negative 18 (false negative) 32 (true negative) NPV = 64% Sensitivity = 51% Specificity = 94% Abbreviations: NPV, negative predictive value; PCR, polymerase chain reaction; PPV, positive predictive value. Although the standard approach in our institution was to only send samples with negative cultures for broad-range PCR, on review 11 samples were actually culture positive. The growth in these cultures usually occurred after at least several days of incubation, by which time samples had already been sent for PCR testing. Of 19 patients with true-positive PCR results, 6 patients also had positive cultures; 4 of these were concordant with the PCR (2 *M. tuberculosis* isolates from a psoas abscess and spinal tissue, *Streptococcus pneumoniae* from hip tissue, and *Pseudomonas aeruginosa* from a tibial sample) and 2 were discordant (*Cryptococcus neoformans* from bronchoalveolar lavage and *Rhizopus oryzae* from sinus tissue, both identified by PCR but not cultures). The isolates identified in the 5 culture-positive, PCR-negative specimens included 1 *Mycobacterium avium* complex, 2 *Propionibacterium acnes*, 1 *P. aeruginosa*, and 1 coagulase-negative *Staphylococcus*. A comparison of patient characteristics stratified by PCR results is shown in [Table 3](#T3){ref-type="table"}. The only factors significantly associated with a positive PCR result were high PMN count and signs of inflammation on histopathologic examination. No significant differences were detected between PCR result and specimen site (orthopedic vs nonorthopedic) or nature of the specimen (fresh vs paraffin-embedded), macroscopic operative findings, or inflammatory markers. Antibiotic therapy was significantly more likely to be modified in patients with positive PCR results compared with those with negative results (52% vs 14%; OR, 6.44; *P* = .002). Details of the specific cases where the result clearly affected management are shown in [Table 4](#T4){ref-type="table"}. In total, 18/71 patients (25%) had management alterations due to PCR results. ###### Patient Characteristics Stratified by Universal PCR Result Characteristic PCR Negative (n = 50) PCR Positive (n = 21) Odds Ratio (95% CI) *P* Value --------------------------------------------------------------- ----------------------- ----------------------- ------------------------ ----------- Age, mean ± SD, y 57.5 ± 15.5 58.7 ± 16.1 1.005 (0.97--1.04) .77 Orthopedic site, No. (%) 27 (54) 8 (38) 0.52 (0.18--1.46) .22 ≥3+ PMNs on gram stain (n = 60), No. (%) 5/43 (12) 6/17 (35) 4.17 (1.06--16.67) .04 CRP 48 ± 50 73 ± 62 1.008 (0.997--1.019) .13 ESR 58 ± 33 67 ± 36 1.0079 (0.9888--1.028) .42 Pathologic signs infection, No. (%) 16/37 (43) 13/16 (81) 5.69 (1.52--27.96) .02 Operative signs of infection, No. (%) 18/41 (44) 7/13 (54) 1.49 (0.42--5.39) .53 Receiving antibiotics at time of specimen collection, No. (%) 29 (58) 13 (62) 1.18 (0.42--3.45) .76 Antibiotic change following result, No. (%) 7 (14) 11 (52) 6.44 (2.05--21.89) .002 FFPE sample (vs fresh), No. (%) 8 (16) 5 (24) 0.61 (0.18--2.27) .44 Abbreviations: CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; FFPE, formalin-fixed, paraffin-embedded; PCR, polymerase chain reaction; PMN, polymorphonuclear leukocyte. ###### Description of the 18 Patients in Whom PCR Results Had Significant Impact on Antibiotic Therapy Diagnosis Initial Antibiotics Culture Result PCR Result Antibiotic Change ------------------------------------------------------------------------------ ------------------------------------------------------ --------------------------------------------------------------- ------------------------------------------------------------------- --------------------------------------------------------------------------------------- Nonunion following open tibial fracture Vancomycin, cefepime No growth *Staphylococcus pettenkoferi*, *Staphylococcus pseudolugdunensis* Vancomycin/cefepime stopped, linezolid started Knee swelling in the setting of PTLD Vancomycin, cefepime No growth Negative Antibiotics stopped Disseminated fungal infection Linezolid, micafungin, voriconazole No growth *Cunninghamella* Patient expired before change could be made^a^ Right prosthetic knee joint infection Vancomycin, ampicillin No growth *Streptococcus mitis* Changed to ceftriaxone^b^ Left hip pain (native joint) Vancomycin No growth Negative Antibiotic stopped Imaging evidence of 1-cm right frontal lobe mass, with question of granuloma None No growth Negative No antibiotic was started, and patient was discharged from ID clinic after PCR result Brain abscess Vancomycin, ceftriaxone, metronidazole, levofloxacin No growth *Fusobacterium nucleatum* Vancomycin/levofloxacin stopped, ceftriaxone/metronidazole continued Pelvic abscess Vancomycin, cefepime *Streptococcus pneumoniae* *Streptococcus pneumoniae* Cefepime stopped, vancomycin continued Treated left MSSA septic knee, tested before revision Cefazolin No growth Negative Antibiotic stopped Destructive cervical spine lesion by imaging Vancomycin, ceftriaxone No growth Negative Antibiotics stopped Pelvic abscess Ciprofloxacin, meropenem, daptomycin, micafungin No growth *Ureaplasma urealyticum*, *Aspergillus fumigatus* Changed to moxifloxacin, fluconazole^c^ Right ankle infection with hardware in situ Vancomycin No growth *Propionibacterium acnes* Changed to penicillin HIV with pneumonia None *Haemophilus influenzae*, *lactobacillus*, *Candida glabrata* *Cryptococcus neoformans* Fluconazole started following PCR result Left hip prosthetic infection Vancomycin, ertapenem No growth *Mycobacteria avium* complex Rifampin and azithromycin started Rheumatoid arthritis with failed multiple therapies to rule out infection None No growth Negative ID cause was ruled out T10-T11 osteomyelitis with hardware in situ Vancomycin, ertapenem No growth *Propionibacterium acnes* Changed to penicillin Question of right prosthetic joint infection Daptomycin, meropenem No growth Negative De-escalated to daptomycin and ciprofloxacin Left ankle septic joint with exposed hardware Cipofloxacin, bactrim No growth *Streptococcus agalactiae* Changed to amoxicillin Abbreviations: ID, infectious diseases; PCR, polymerase chain reaction; PTLD, post-transplant lymphoproliferative disorder; T10, 10th thoracic vertebra; T11, 11th thoracic vertebra. ^a^Included in table due to actionable result despite death before change could be made. ^b^Changed to ceftriaxone for ease of administration, not due to suspicion of ampicillin resistance. ^c^ *Aspergillus* was thought to be a contaminant given the clinical picture; no treatment for *Aspergillus* was initiated, but fluconazole was added instead of micafungin for possible intra-abdominal candidasis. DISCUSSION {#s7} ========== Obtaining an accurate microbiologic diagnosis is 1 of the key factors informing choice of antimicrobial therapy in patients with serious infections. Though it is costlier than culture-based methods, our findings suggest that broad-range PCR is a valuable addition to the diagnostic workup of patients with culture-negative infections. Although some studies have suggested that PCR is not superior to culture \[[@CIT0021], [@CIT0026]\], in our cohort, use of the broad-range PCR assay led to identification of infecting pathogens in approximately half of the patients who were clinically suspected of having infection. Had the assay not been performed, it is possible that 1 patient would have been inappropriately untreated, 4 patients would have been overtreated based on suspected infection, and 11 patients would have been treated with a less effective or inappropriate antibiotic regimen. Given the serious consequences of untreated infections, the broad-range PCR assay was of considerable value in our patient population. It also demonstrated significant value from an antibiotic stewardship perspective, especially in PCR-positive cases, leading to de-escalation in 8 cases, change from intravenous to oral in 3 cases, starting appropriate therapy in 1 case, and stopping antibiotics in 4 cases. This study is 1 of the first to examine the performance and clinical impact of broad-range PCR in real-world clinical practice, in a setting where most patients had negative cultures \[[@CIT0010], [@CIT0011], [@CIT0028]\]. Previous studies have demonstrated the ability of broad-range PCR to identify organisms from heart valve tissue \[[@CIT0011], [@CIT0014]\], joint tissue \[[@CIT0012]\], and other sterile sites, with sensitivity and specificity ranging from 43% to 96% and 72% to 95%, respectively. However, these studies typically compared PCR results with standard culture results as a gold standard. In this study, we reviewed each case in detail and used a "composite clinical diagnosis" as the gold standard rather than only culture results, allowing us to calculate a more realistic sensitivity and specificity than prior studies, which likely explains why our values were somewhat lower than what has been previously described. Our findings suggest that a positive result is more clinically impactful than a negative result and plays a bigger role in antimicrobial decision-making. In our cohort, the likelihood of obtaining a positive result was significantly higher in patients with signs of inflammation on microbiologic or histological examination. These findings are consistent with prior studies \[[@CIT0017], [@CIT0020], [@CIT0046]\]. Factors such as these could be taken into consideration by ordering clinicians aiming to increase the diagnostic yield. Although there have been some studies that reviewed the effect of the PCR result on antibiotic management \[[@CIT0027], [@CIT0028], [@CIT0047]\], none of these assessed if there was any difference in antimicrobial management between patients testing PCR positive vs negative. There are some important limitations that should be kept in mind when interpreting these results. Statistical power was limited by a relatively small sample size, and given the retrospective nature of the study, all available tests were not performed on all samples. Selection bias may influence interpretation of our results and generalizability, as many of our patients were complex with multiple comorbidities, prolonged hospitalization, and antimicrobial exposure. Although we attempted to approximate a true gold standard, incorporating all available clinical information, in some cases it was difficult to truly know if infection was present or absent. Despite the fact that this test was supposed to be performed only in culture-negative patients, there were 11 cases with positive cultures; although it may have been clinically justified to order the broad-range PCR despite this in some cases, it is important for clinicians to remember to wait sufficient time for initial cultures to be finalized in order to avoid performing PCR unnecessarily. Although antimicrobial changes were temporally associated with PCR results' availability, it is possible that other unmeasured factors influenced this decision-making. Finally, we were unable to assess other clinical outcomes beyond antibiotic selection. In summary, our findings suggest that broad-range PCR is a clinically useful test that has an important role in the diagnostic evaluation of patients with culture-negative infections. Optimizing specimen selection by considering the full clinical scenario including microbiological and histopathological data can increase the likelihood of a positive result, which in our population had the biggest impact on antimicrobial decision-making. Infectious diseases physicians should carefully consider these advantages and limitations on an individualized basis before requesting this complex, difficult to interpret, and expensive test. Supplementary Data {#s8} ================== Supplementary materials are available at *Open Forum Infectious Diseases* online. Consisting of data provided by the authors to benefit the reader, the posted materials are not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author. ###### Click here for additional data file. The authors would like to acknowledge Winston Edwards for help with specimen identification, Dhruba J. SenGupta, PhD, for PCR method description, and Jacob Garrell for assistance with manuscript editing. ***Financial support*. **This work was supported by the Tufts Medical Center Division of Geographic Medicine and Infectious Disease Francis P. Tally MD Fellowship. ***Potential conflicts of interest.* **All authors: no reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed. ***Prior presentation*:** This work was previously presented at ID Week, and the abstract was published by *Open Forum Infectious Diseases* (Clinical utility of universal PCR and its real-world impact on patient management. Open Forum Infect Dis 2017; 4(Suppl 1):S627).
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The world in which workers lived influenced their efforts to organize. Employers needed constant production to satisfy consumer demand in boom times. In bad economic times, jobs disappeared and workers suffered. Wars forced employers and workers to compromise. Immigration added cheap labor to the marketplace. Social change movements made people more aware of unfair or unsafe practices. All of these factors and more played a role in the rise of organized labor. Some of these factors contributed to the decline of unions. Follow the timelines to see what happened. explore now
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Ramsons (Wild Garlic) Allium ursinumBelongs to the onion family. An annual (sometimes biennial) onion relative that grows wild in shady, moist and nutrient-rich top soil, especially in decidious forests. It is quite rare, but when it thrives, it can occur in large populations covering the ground in spring.Wild garlic is harvested in spring and early summer, is 15-45 cm high and has, unlike the chives, large broad leaves and white flowers. Everything can be used: the elongated bulb, the leaves and also flower stalks with closed buds. It has a nice, mild garlic flavour and similar medicinal properties. It's propagated by seeds and bulbs. SOWING: The seeds need to be brought out of suspension with cold spells. Either directly sown in the autumn or very early spring. For normal spring sowing, some weeks in the refrigerator's freezer compartment, sown in light soil, will make the seeds believe that it has been winter. SEEDS: 1 g is about 150 seeds. Ramsons, organic seedTemporarily unavailable Belongs to the Onion family, it is a perennial (sometimes biannual) relative of the onion which grows wild in shadowy and nutrient- and humus-rich soil, predominantly in deciduous forests. It is quite...
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Technical computing environments are known that present a user, such as a scientist or engineer, with an environment that enables efficient analysis and generation of technical applications. For example, users may perform analyses, visualize data, and develop algorithms. Technical computing environments may allow a technical researcher or designer to efficiently and quickly perform tasks such as research and product development. Existing technical computing environments may be implemented as or run in conjunction with a graphically-based environment. For example, in one existing graphically-based technical computing environment, graphical simulation tools allow models to be built by connecting graphical blocks, where each block may represent an object associated with functionality and/or data. Blocks may be hierarchical in the sense that each block itself may be implemented as one or more blocks. A user may, for instance, view the model at a high level, then select blocks to drill down into the model to see increasing levels of model detail. Models generated with graphical simulation tools may be directly converted to computer code by the graphical simulation tool, which can then be executed in the target environment. For example, a model of a control system for an automobile may be graphically developed with the graphical simulation tool, implemented as code, and then deployed in an embedded system in the automobile. It is often desirable that a graphical model be tested or verified before a system using the model is deployed. One technique for verifying a model is based on a coverage analysis of the model. In general, coverage analysis may provide a measure of how complete test data input to the model was in testing the model. Knowing the completeness of testing can be important in determining whether a model is ready to be implemented in a “live” system. For example, if the coverage analysis indicates that certain portions of the model or the code used to implement the model were not used when the model was run with the test data, it may be desirable to revise the model or the test data to obtain more complete coverage. A concept related to model coverage is code coverage. Code coverage analysis may be used to dynamically analyze the way that a program executes. Similar to model coverage analysis, with code coverage analysis, it may be desirable to determine the completeness with which program code was executed during testing.
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Dying Stars ‘Key to Finding Alien Life’ A telescope will be able to see if a planet has oxygen and water in just a few hours (David A. Aguilar CfA) Dying stars are humanity's best bet at finding alien life in the near future, researchers have said. Astronomers at the Harvard-Smithsonian Centre for Astrophysics (CfA) say life could be detected within the next 10 years on planets orbiting white dwarf stars. Planets orbiting white dwarfs offer the best hope of finding extraterrestrials because scientists can detect oxygen in their atmosphere fairly easily. In comparison, it is very hard to find oxygen on planets orbiting sun-like stars or red dwarfs. Before a star turns into a white dwarf, it swells into a red giant and engulfs and destroys nearby planets. The Cfa recently found that the closest habitable planet was orbiting a red dwarf. Although these types of stars are much smaller and fainter than the sun, it is much bigger than a white dwarf and its glare would overwhelm any signal from an orbiting planet's atmosphere. Theorist Avi Loeb said: "In the quest for extraterrestrial biological signatures, the first stars we study should be white dwarfs. "Although the closest habitable planet might orbit a red dwarf star, the closest one we can easily prove to be life-bearing might orbit a white dwarf." When a star such as our sun dies, it "puffs off" its outer layers and leaves behind a hot core - a white dwarf. White dwarfs are about the same size as Earth and they slowly cool and fade over time - billions of yearsm which allows it to retain heat long enough to warm a nearby world. Chemical fingerprint A planet would have to be fairly close to a white dwarf for it to have liquid water on its surface and would circle the star about once every 10 hours. If a planet did exist in the habitable zone, it would be fairly easy to find - if an Earth-like planet passed an Earth-sized star it would block a large fraction of its light. It is estimated that there are one or more potentially habitable planets orbiting the nearest 500 white dwarfs. When the white dwarf shines light through the ring of air surrounding the planet, the atmosphere absorbs some of it, leaving a chemical fingerprint that would tell whether there is water vapour in the air.
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There are 26 countries in Sub-Saharan Africa in which French is an official language. Of the 16 countries in West Africa, 9 are considered to be francophone – Benin, Burkina Faso, Ivory Coast, Guinea, Mali, Niger, Senegal, and Togo. The French colonial system was a “very centralized, unified and bureaucratic system whose aim was the assimilation of native people [mission civilisatrice] and whose method was direct rule” (Dimier, 2004, p. 279 as cited in Wolf, 2008, p. 557). In addition to the various French administrators, support for French colonial rule was also provided by traditional African rulers (e.g. local chiefs) who “became agents for the transmission of French commands to their African subjects and in time became Western-educated subordinates” (Clark & Gardinier, 1997, p. 10). A key tool in the French mission civilisatrice was the use and promotion of the French language, especially in education. Georges Hardy, a French colonial inspector of public instruction in Western French Africa in the early 1900s, defined school as A means to transform the primitive people [of West Africa]…in order to render them devoted to our cause and to our mission, in order that they, over a period of years, succumb to our intellectual and moral ways; in a word, the school will form his spirit and mind in accordance to our intention (as cited and translated in Locraft, 2005, p. 13). Following this definition, French was the official language of instruction at all levels of education. Today most of these countries continue to use French as an official language in administration and education, despite the fact that it is only spoken by an estimated 79 million people in all of Sub-Saharan Africa (out of a total population of over 900 million) (Organisation Internationale de la Francophonie; World Bank). Trudell (2012) attributes this lack of change, at least in part, to the French state, which has an “ongoing influence of…political and financial investment in francophone Africa” (p. 374). She also identifies the Organisation Internationale de la Francophonie (OIF), which seeks to “strengthen and enhance the teaching and use of the French language in the world as well as in the diplomatic and international life where the role of French is contested” (translation mine, http://www.francophonie.org/-Langue-francaise-et-multilinguisme-.html) The average rate of drop-out in primary schools of French-speaking countries is nearly 25 percent according to most World Bank and UNESCO annual reports. In Francophone Africa, the majority of primary school students experience exclusion in the classroom. Owing to a lack of proficiency in French, they are silenced and spend most of their time listening to the teacher and the very few students who can speak French (p. 107). In this way, language policies serve to further exacerbate existing socio-economic divisions and hierarchies. Some countries, such as Burkina Faso and Mali, have developed experimental bilingual programs with relatively positive results. These minor successes, however, have not translated to more widespread policies and practices, and French continues to be the primary medium of instruction in schools. Wolf, H.G. (2008). British and French language and educational policies in the Mandate and Trusteeship Territories. Language Sciences (30), p. 553-574. REFERENCE AND COPYRIGHT INFORMATION FOR THIS PAGE This web page has a copyright. It may be referred to and quoted, or reproduced and distributed for educational purposes according to fair use legislation only if the following citation is included in the document: This information was originally published on the website of the International Network for Language Education Policy Studies (http://www.languageeducationpolicy.org) as
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Dungan language The Dungan language ( or ) is a Sinitic language spoken primarily in Kazakhstan and Kyrgyzstan by the Dungan people, an ethnic group related to the Hui people of China. Although it is derived from the Central Plains Mandarin of Gansu and Shaanxi, it is written in Cyrillic (or Xiaoerjing) and contains loanwords and archaisms not found in other modern varieties of Mandarin. History The Dungan people of Kyrgyzstan and Kazakhstan (with smaller groups living in other post-Soviet states) are the descendants of several groups of the Hui people that migrated to the region in the 1870s and the 1880s after the defeat of the Dungan revolt in Northwestern China. The Hui of Northwestern China (often referred to as "Dungans" or "Tungani" by the 19th-century western writers as well as by members of Turkic nationalities in China and Central Asia) would normally speak the same Mandarin dialect as the Han people in the same area (or in the area from which the particular Hui community had been resettled). At the same time, due to their unique history, their speech would be rich in Islamic or Islam-influenced terminology, based on loanwords from Arabic, Persian, and Turkic languages, as well as translations of them into Chinese. The Hui traders in the bazaars would be able to use Arabic or Persian numbers when talking between themselves, to keep their communications secret from Han bystanders. While not constituting a separate language, these words, phrases and turns of speech, known as Huihui hua (, "Hui speech"), served as markers of group identity. As early 20th century travellers in Northwestern China would note, "the Mohammedan Chinese have to some extent a vocabulary, and always a style and manner of speech, all their own". As the Dungans in the Russian Empire, and even more so in the Soviet Union, were isolated from China, their language experienced significant influence from the Russian and the Turkic languages of their neighbors. In the Soviet Union, a written standard of the Dungan language was developed, based on a dialect of the Gansu province, rather than the Beijing base of Standard Chinese. The language was used in the schools in Dungan villages. In the Soviet time there were several school textbooks published for studying the Dungan language, a three volume Russian–Dungan dictionary (14,000 words), the Dungan–Russian dictionary, linguistics monographs on the language and books in Dungan. The first Dungan-language newspaper was established in 1932; it continues publication today in weekly form. When Dru C. Gladney, who had spent some years working with the Hui people in China, met with Dungans in Almaty in 1988, he described the experience as speaking "in a hybrid Gansu dialect that combined Turkish and Russian lexical items". Mutual intelligibility with Mandarin dialects There is a varying degree of mutual intelligibility between Dungan and various Mandarin dialects. The Shaanxi and Gansu Mandarin dialects are understood by Dungans. On the other hand, Dungan speakers like Yasyr Shivaza and others have reported that Chinese who speak the Beijing Mandarin dialect can understand Dungan, but Dungans could not understand the Beijing Mandarin. Demographics Dungan is spoken primarily in Kyrgyzstan, with speakers in Russia, Kazakhstan and Uzbekistan as well. The Dungan ethnic group are the descendants of refugees from China who migrated west into Central Asia. According to the Soviet census statistics from 1970 to 1989, the Dungan maintained the use of their ethnic language much more successfully than other minority ethnic groups in Central Asia; however, in the post-Soviet period, the proportion of Dungans speaking the Dungan language as their native language appears to have fallen sharply. Grammar Classifiers Chinese varieties usually have different classifiers for different types of nouns, with northern varieties tending to have fewer classifiers than southern ones. () is the only classifier found in the Dungan language, though not the only measure word. Phonology In basic structure and vocabulary, the Dungan language is not very different from Mandarin Chinese, specifically a variety of Zhongyuan Mandarin (not Lan-Yin Mandarin) spoken in the southern part of the province of Gansu and the western part of the valley of Guanzhong in the province of Shaanxi. Like other Chinese varieties, Dungan is tonal. There are two main dialects, one with 4 tones and the other, considered standard, with 3 tones in the final position in phonetic words and 4 tones in the nonfinal position. Consonants The corresponding table compares current Dungan spelling, old Dungan spelling, pinyin and IPA. Vowels Using Standard Chinese vowels as basis, each vowel and its respective current Dungan spelling is presented below, along with the old Dungan spelling, using pinyin and IPA. Note that the correspondence between Dungan vowels and Standard Chinese vowels is not perfect. Vowel constructs that can be used as independent syllable without consonants are shown in parenthesis. There are rhotacised vowels, as well as some syllables only seen in loan words from Russian, Arabic, Kyrgyz, etc., in addition to the above table. Tones Tones in Dungan are marked with nothing (tone 1), a soft sign (tone 3) and a hard sign (tone 2). Vocabulary The basilects of Gansu/Shaanxi Mandarin and Dungan are largely mutually intelligible; Chinese journalists conversant in one of those Mandarin dialects report that they can make themselves understood when communicating with Dungan speakers. However, even at the level of basic vocabulary, Dungan contains many words not present in modern Mandarin dialects, such as Arabic and Persian loanwords, as well as archaic Qing dynasty-era Chinese vocabulary. Furthermore, the acrolects of Dungan and Gansu/Shaanxi Mandarin have diverged significantly due to time and cultural influences. During the 20th century, translators and intellectuals introduced many neologisms and calques into the Chinese language, especially for political and technical concepts. However, the Dungan, cut off from the mainstream of Chinese discourse by orthographic barriers, instead borrowed words for those same concepts from Russian, with which they came into contact through government and higher education. As a result of these borrowings, the equivalent standard Chinese terms are not widely known or understood among the Dungan. Writing system The modern Dungan language is the only spoken Chinese that is written in the Cyrillic alphabet, as they lived under Soviet rule. It is a Russian-based alphabet plus five special letters: Җ, Ң, Ү, Ә and Ў. As such, it differs somewhat from the Palladius System that is normally used in Russia to write Chinese in Cyrillic. Note The letters Ъ and Ь are only used to write Russian loanwords and tone markings on children's primers dictionaries Dungan is unique in that it is one of the few varieties of Chinese that is not normally written using Chinese characters. Originally, the Dungan, who were Muslim descendants of the Hui, wrote their language in an Arabic-based alphabet known as Xiao'erjing. The Soviet Union banned all Arabic scripts in the late 1920s, which led to a Latin orthography based on Janalif. The Latin orthography lasted until 1940, when the Soviet government promulgated the current Cyrillic-based system. Xiao'erjing is now virtually extinct in Dungan society, but it remains in limited use by some Hui communities in China. The writing system is based on the standard 3-tone dialect. Tones marks or numbering do not appear in general-purpose writing, but are specified in dictionaries, even for loanwords. The tones are specified using the soft sign, hard sign, or nothing. Consonant chart: Literature A number of books in Dungan language, including textbooks, Dungan-Russian and Russian-Dungan dictionaries, a Dungan etymological dictionary, collections of folk tales, original and translated fiction and poetry have been published in Kyrgyzstan. Usual print runs were no more than a few hundred copies. A newspaper in Dungan has been published as well. Works of the Dungan poet Yasir Shiwaza have been translated into Russian, Standard Chinese, and a number of other languages, with print runs in some of them been much higher than in the original Dungan. English translations of some of them, along with the original Dungan text, are available in the book by S. Rimsky-Korsakoff (1991). See also Cyrillization of Chinese Notes General references Svetlana Rimsky-Korsakoff Dyer, Iasyr Shivaza: The Life and Works of a Soviet Dungan Poet. 1991. . (Contains a detailed bibliography and ample samples of Shivaza works', some in the original Cyrillic Dungan, although most in a specialized transcription, with English and sometimes standard Chinese translations). Olga I. Zavjalova. "Some Phonological Aspects of the Dungan Dialects." Computational Analyses of Asian and African Languages. Tokyo, 1978. No. 9. Pp. 1–24. (Contains an experimental analysis of Dungan tones). Olga Zavyalova. “Dungan Language.” Encyclopedia of Chinese Language and Linguistics. General Editor Rint Sybesma. Vol. 2. Leiden–Boston: Brill, 2017. Pp. 141–148. 海峰。 中亚东干语言研究 (Hai Feng. Zhongya Donggan yuyan yanjiu—A Study of the Dungan Language of Central Asia.) Urumchi, 2003. 479 p. . (Description of the Dungan language by a professor of Xinjiang University). External links "Implications of the Soviet Dungan Script for Chinese Language Reform": long essay on Dungan, with sample texts Dungan writing system in Omniglot The Shaanxi Village in Kazakhstan Soviet census data for mother tongue and second language, in English Central Asian Dungan as a Chinese Dialect Category:Languages of Kyrgyzstan Category:Languages of Kazakhstan Category:Mandarin Chinese Category:Languages of Russia Category:Languages of Tajikistan Category:Languages of Turkmenistan Category:Languages of Uzbekistan
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Siege of Pizzighettone The Siege of Pizzighettone was the first major military engagement of the northern Italian campaigns of the War of the Polish Succession. Troops from France and the Kingdom of Sardinia began blockading the Habsburg Milanese fortress at Pizzighettone on 11 November 1733, commencing siege operations on 15 November. On 30 November the commander of the Austrian garrison negotiated a capitulation in which he promised to withdraw toward Mantua on 9 December if no relief arrived. As no reinforcements appeared by that time, the fortress' garrison withdrew with full honors on 9 December. References Military campaigns of Prince Eugene of Savoy, Volume 19 Siege of Pizzighetone Category:Battles in Lombardy Category:Sieges involving France Category:Sieges involving Austria Category:Battles of the War of the Polish Succession Category:1733 in Europe Category:Duchy of Milan Category:Battles involving the Kingdom of Sardinia
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Big Data Hadoop Training Institute Big Data Hadoop Training will enable you to master the concepts of the Hadoop framework and its deployment in a cluster environment. Apache Hadoop or Hadoop is a collection of open source software which functions using a joint network of many computers to solve monumental issues regarding massive amounts of data and computation. It provides a generic framework for digital storage and processing big data bits using the map reduce programming tool. It was originally designed for computer clusters built from common hardware; Apache Hadoop has also found its roots on various higher end hardware too. ExlTech’s Big Data Hadoop Training All the modules of Hadoop are designed with a common aim at mind to be automatically handled by the Hadoop framework. The core programming of Apache Hadoop consists of a storage part known widely as Hadoop Distributed File System (HDFS) and a processing part which is a Map Reduce programming model. Hadoop splits files into large blocks of data and distributes them across nodes in a cluster based system. This gives the advantage of data locality where nodes are easily manipulated into the data on the access they have. This allows faster dataset processing with more efficiently than it would be in a more conventional supercomputer architecture which relies on a parallel file system where computation and data are distributed via high-speed networking. All the required certification and inputs required for a successful industry experience would be provided at ExlTech. What is Big Data Hadoop? Hadoop is an open-source framework that was manufactured by the Apache Software Foundation. It is one of the tools used to handle big data which consists of both structured and unstructured data. This collection of data cannot be processed or stored by traditional methods.
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Can You Hear Me Now? Detecting Hidden Hearing Loss in Young People Even during the simple act of commuting to work, we can’t escape the ubiquitous noise that invades our lives: Traffic rumbling down the street, a jackhammer at a construction site, the roar of the subway—not to mention music and podcasts we pump directly into our ears. Yet for many years conventional wisdom has held that as long as we could pass a hearing test, everything was fine. That is until 2009 when researchers uncovered a phenomenon called “hidden” hearing loss—a likely contributor to the cumulative loss typically associated with aging. Now, scientists at Massachusetts Eye and Ear hospital have developed a suite of tools for detecting hidden hearing loss, an important step in figuring out the magnitude of the problem and what we can do to fix it. They reported their findings this week in PLoS ONE. Hearing loss is most often associated with damage to so-called hair cells inside our ears, which detect vibrations in the environment and translate them into chemical signals that prompt our auditory nerves to fire. During an audiogram—considered the gold standard of hearing tests—patients listen to sounds of different frequencies at different volumes to determine their thresholds for sound detection. Those with damaged hair cells tend to have trouble detecting low-volume sounds at certain frequencies. Damage to our hearing, however, actually starts long before our hair cells are affected, research suggests. First there is damage to the fibers in the auditory nerve that connect to hair cells and help us hear in noisy environments—hence the “hidden” in hidden hearing loss. This phenomenon remained obscure for so long because an audiogram administered in a quiet room does not activate these auditory nerve fibers, which means patients can pass a hearing test even when the fibers have been damaged. Previous research has found signs of such hidden hearing loss in mice, guinea pigs, chinchillas and postmortem human ear tissue. Now auditory physiologist and study co-author Stéphane Maison and his colleagues have taken the next logical step: investigating hidden hearing loss in human patients. “In the end, the main goal is to have a measure of hidden hearing loss that is currently not available in [the] clinic,” Maison says. To test the tools they developed, the researchers divided 34 volunteers ranging from ages 18 to 41 into two groups: a low-risk one composed of college students studying “quiet subjects” (such as communication science) and a high-risk group mostly consisting of music students exposed to loud sounds for four to six hours per day. Both groups passed their audiograms with flying colors. When the researchers extended the test to include higher frequencies than are normally evaluated, however, the high-risk group had trouble hearing the sounds at low volumes. The researchers also outfitted subjects with electrodes to measure how each volunteer’sauditory nerve responds to sound (which they compared with the response of the hair cells for each individual to reduce variability). The auditory nerves of subjects in the high-risk group did not respond to sound as robustly as those of subjects in the low-risk group. Perhaps most striking, when subjects were asked to listen to words and repeat them back while noise played in the background, the high-risk group performed significantly worse than the low-risk group. The same was true when the words were sped up and played with a background echo. On a questionnaire that accompanied the tests, the high-risk group indicated they were more “bothered” by everyday sounds like a dog barking or a baby crying than the low-risk group was. Cumulatively, these results not only reveal hidden hearing loss can start at a young age but also that it is not so hidden after all—it adversely affects our hearing in numerous ways, including the ability to detect high-frequency sounds and hear in noisy settings. In a quiet place, Maison says, “you’re not going to notice it, but when you’re going to go to a bar or a restaurant, and there’s a lot of background noise, you’re going to struggle.” Gabriel Corfas, a researcher at the University of Michigan’s Kresge Hearing Research Institute who was not affiliated with the study, thinks this work is an important step in the field of hidden hearing loss. “It raises the issue of how exposing ourselves as young people to noise levels that we don’t think of being extreme—through education, through entertainment, through work—could actually impact our hearing throughout our life,” he says, “and brings to the forefront the need to discuss how much we expose ourselves to noise, and how to protect ourselves.” On an individual level, protecting ourselves from hidden hearing loss could entail limiting noise exposure and using ear protection. On a society-wide scale, it may necessitate revisiting current standards regulating noise in the workplace. Fortunately, even after hidden hearing loss has occurred, the picture is not entirely bleak. Corfas and his team have previously reported that treating the ears of mice exposed to loud environments with a growth factor called neurotrophin 3 can reverse hidden hearing loss by repairing some of the damage to auditory nerve fibers. Corfas is hopeful that a similar therapy could ultimately be used in humans and could, in theory, be an important step in preventing age-associated hearing loss. He points out that tools to diagnose hidden hearing loss—such as those developed by Maison’s team—would be essential for testing such therapies and detecting damage at an early stage when it is more treatable.
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By admin Robotics was the brainchild of engineering and philosophy, STEM and the humanities, the objective and the subjective. In 1948, Norbert Weiner proposed the idea of robotics, and George Devol brought those ideas to life 6 years later in 1954.Since then robotics has gained the potential to change the world forever when the idea of artificial intelligence emerged into the aether of ideas. The field of robotics went from any other subdivision of engineering into artificial intelligence, a revolutionary breakthrough that could change society.Now, before we continue, we must clearly define the difference between the two fields. Robotics is simply using engineering to create machines that have a set code of actions that include physical movement and a limited set of words their creator put in their code.Artificial intelligence is the term describing robots who have an ever-expanding set of actions they can take, with their code allowing them to learn new skills on their own. With robots, you yourself would have to add these actions to their code.Once artificial intelligence was introduced and the first artificially intelligent robots were created, scientists and philosophers began discussing the possibility of having these robots take up the jobs humans work: From simple jobs like a janitor to complex jobs like a journalist.This question was met with a hoard of infuriated, anxious ""s. The status quo screamed with horror that it would ruin the economy, and the more fringe of the status quo (ironic as that sounds) warned it would lead to AI becoming so sophisticated that it took over human civilization.I will not discuss the economic side. rather I will address the fear that AI would become so sophisticated that it would revolt against humanity and make us obsolete. This is, as much as I originally presented as fringe, a very reasonable fear.With artificial intelligence, you have a machine that is constantly gaining new abilities and talents. Nothing, absolutely nothing, is stopping it from becoming capable of rebelling against the species its creator belonged to creating a brave new world.So, we must rely on robots. Robots have a limited set of skills. They only know what we teach them. If we never inform them on how to perform that task by implementing it into their code, then they'll never learn. So we simply avoid teaching them how to rebel and we'll be fine.The world of robotics is a wonderful opportunity for the human race. Robots could take up the jobs we have no will to do and allow us to live wonderous lives of decadence and luxury. Automation is not our enemy, it is not out friend, it is our servant.
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Heretofore there have been a number of different types of electromagnetic launchers with rails. FIG. 12 schematically illustrates the general construction of a conventional electromagnetic railgun. The railgun includes a pair of rails 1 and 2 positioned parallel to and spaced apart from one another. Rails 1 and 2 form barrel 3 which includes breech end 4 and muzzle end 5. Armature 6 is sized so as to slide between rails 1 and 2. The armature 6 and the projectile 7 may be combined into one body, or may be the same body. Rails I and 2 are connected to a source of electrical power 8. The next explanation will define the operation. When the armature 6 is in the barrel 3, current begins to flow between the rails and 2 through the armature 6. This current produces a magnetic field to the left of the armature. This magnetic field interacts with the current flowing through the armature via path 9, to create an electromagnetic force that causes the armature to accelerate to the right along barrel 3, and out of the muzzle end 5 of the railgun. In another type of railgun, known as a plasma armature railgun, current flows along path 10 through a plasma created by the electric current between the rails to the left of an electrically insulating projectile 7 which is used in place of the armature 6. Current running through the plasma interacts with the magnetic field generated by the current in the rails and results in acceleration of the plasma, and therefore of the insulating projectile, to the right along barrel 3. A primary objective of electromagnetic launcher design is to maximize efficiency by minimizing energy losses in the electromagnetic launcher system. Some sources of energy loss in an electromagnetic launcher system are: resistive losses in the rails and any supply conductors, loss in the plasma behind the projectile and/or in the armature of projectile PA1 loss of the energy due to the force of friction between the projectile and the walls of the barrel bore PA1 loss of energy stored in the magnetic field from the rail current, which is dissipated in muzzle resistors after each shot. The present invention reduces the energy stored in the magnetic field from the rail current. In U.S. Pat. No. 4,796,511 to Eyssa, the author makes an attempt to reduce these losses by segmentation of the rails and by special supply conductors (See FIG. 13). Both supply conductors 11 and 12 have two semi-cylindrical portions: 13 and 14 for supply conductor 11, and 15 and 16 for supply conductor 12, respectively. The portions 13 and 14 are electrically connected with segmented rail 17 and the portions IS and 16 are electrically connected with segmented rail 18. These semi-cylindrical portions are disposed on either side of the projectile path between the rails and in generally coaxial relationship to one another. The author supposes that because the semi-cylindrical portions are coaxially arranged the magnetic field from current in such portions will not exist inside of barrel. Because the currents flow in opposite directions in nonsymmetrical coaxial supply conductors, the currents are repelled by one another and the density of current will be distributed as shown in FIG. 13. These currents will create a magnetic field 19 inside the barrel and the stored magnetic energy will be lost after each shot.
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Sugar-sweetened beverages and body weight. Given the high prevalence of obesity in the USA, much recent attention has focused on dietary strategies for weight control. Several medical and scientific societies currently recommend reducing consumption of sugar-sweetened beverages (SSBs). However, the evidence base for a public health recommendation has been a topic of debate. The purpose of this review is not to underscore the debate but rather to consider how recently published data pertaining to SSBs contribute to the evidence base for preventing and treating obesity, with application to caring for patients. Consumption of SSBs remains prevalent in the USA. Emerging data from epidemiological studies and clinical trials indicate that consumption contributes to positive energy balance and reducing consumption has beneficial effects on body weight. Some individuals may be more susceptible to the adverse effects of consuming SSBs owing to their ethnicity or genetic predisposition. Plausible physiological mechanisms link consumption of SSBs with weight control. Available data provide an evidence base for counselling patients to reduce consumption of SSBs. Nevertheless, additional research is needed to strengthen the evidence base, particularly studies aimed at understanding susceptibility to the adverse effects of consuming SSBs on body weight and mechanisms for these effects.
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Breaking Myths Monday: PTSD PTSD is a psychiatric disorder that affects those who have experienced or witnessed extreme trauma either in their childhood or adult life. These types of traumatic events include situations like natural disasters, serious accidents, terrorist attacks, war, or any type of violent personal assault. Originally referred to as “shell shock” for those who experienced PTSD post-war, PTSD has gotten a reputation to be a veteran’s illness, among other myths. Here are the most common myths about PTSD, and why they’re not true: Myth: PTSD affects someone immediately after trauma, and if it doesn’t happen immediately, they’re no longer at risk. In most cases, symptoms of PTSD will occur within or around the first three months post-trauma. However, this is not the case for everyone, and in cases involving childhood trauma or domestic abuse, the symptoms have a tendency to show up later in life. Symptoms of PTSD are also known to come and go at what seems like random, so it can make it hard for individuals to get diagnosed correctly. Myth: The only people who have PTSD are military veterans. While there is a large percentage of military veterans who experience PTSD, they are not the only people at risk. Trauma can affect anyone. In fact, data shows that around 70% of Americans experience a major event in their lifetime, with 20% of those people developing PTSD. Additionally, women are at a larger risk for developing PTSD because they are more likely to experience physical trauma in their lifetime. Myth: Those who have PTSD are weak individuals. Mental illness is not a character flaw. Those who develop PTSD often have a genetic predisposition to this disorder, or have experienced an extremely traumatic event. This means the development of PTSD was not in their control, and was not their decision. There is no weakness in dealing with trauma. Myth: If you have PTSD you’re dangerous to be around and could lash out at any second. This myth is most likely due to poor representation of PTSD in the media, but is nevertheless extremely inaccurate. The main symptoms associated with PTSD are intrusive thoughts, nightmares, flashbacks, insomnia, guilt, isolation, and hypervigilance. Issues such as aggression and irritability are less common symptoms of PTSD. Myth: PTSD cannot be treated. While there is no cure for PTSD, this does not mean it can’t be treated. PTSD can be managed if an individual is willing to seek help and has a desire to improve. Currently, suggested treatment modalities include cognitive behavioral therapy, prolonged exposure therapy, desensitization therapy, and mood stabilizers or medication. Mental health myths are dangerous because they encourage people to make assumptions about others without doing research, or getting to know the individual. If you have questions about a specific issue or disorder, visit https://sondermind.com/topics where we cover a variety of mental health issues with reputable sources and references.
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Diagnosis and treatment of seborrheic dermatitis. Seborrheic dermatitis is a common skin condition in infants, adolescents, and adults. The characteristic symptoms-scaling, erythema, and itching-occur most often on the scalp, face, chest, back, axilla, and groin. Seborrheic dermatitis is a clinical diagnosis based on the location and appearance of the lesions. The skin changes are thought to result from an inflammatory response to a common skin organism, Malassezia yeast. Treatment with antifungal agents such as topical ketoconazole is the mainstay of therapy for seborrheic dermatitis of the face and body. Because of possible adverse effects, anti-inflammatory agents such as topical corticosteroids and calcineurin inhibitors should be used only for short durations. Several over-the-counter shampoos are available for treatment of seborrheic dermatitis of the scalp, and patients should be directed to initiate therapy with one of these agents. Antifungal shampoos (long-term) and topical corticosteroids (short-term) can be used as second-line agents for treatment of scalp seborrheic dermatitis.
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Esophageal cancer is the eighth most common cancer worldwide and the sixth leading cause of death from cancer. The 2 main histologic types are squamous cell carcinoma and adenocarcinoma. Approximately 90% of cases are esophageal squamous cell carcinoma (ESCC). The survival of patients with ESCC is very poor, largely due to the late development of symptoms and consequent late diagnosis.[@R1],[@R2] Endoscopy is a useful technique for the diagnosis of precancerous esophageal lesions and early cancer. Such lesions may be obscure during screening with white-light endoscopy (WLI), whereas chromoendoscopy techniques have been proven to improve performance of the test.[@R3],[@R4] Computed virtual chromoendoscopy from Fujifilm, called "Flexible spectral imaging color enhancement (FICE) or Fuji intelligent chromoendoscopy," reconstructs the image and displays what the mucosa would look like if it were illuminated using a particular wavelength.[@R5] Moreover, the simplest and most effective method for detecting precancerous lesions and early esophageal cancer is Lugol's chromoendoscopy (LCE).[@R6] Although LCE increases the sensitivity of WLI to \>95%,[@R7] it is uncomfortable for most patients and can cause inflammation of the esophageal mucosa. Above all, the indication of LCE has not yet been well established. It is therefore, important to make the indications for LCE clear and to apply them to high-risk groups. Oral leukoplakia is an established precursor lesion associated with a high risk of oral squamous cell carcinoma,[@R8] and oral leukoplakia is associated with an increased risk of ESCC, particularly in younger people.[@R9],[@R10] Esophageal leukoplakia presents as a "white patch" in the esophageal mucosa that cannot be washed out with water, and its significance has been underestimated. Esophageal leukoplakia is not an unusual phenomenon in Chinese elders during endoscopy screening. Routine LCE has not been performed in most endoscopic centers for each patient with esophageal leukoplakia. FICE has some advantages in determining the shape of a lesion and delineating the lesion's margins. Pale areas via FICE nearly corresponded to esophageal leukoplakia via WLI in our earlier observations, and pale areas were more frequently detected than esophageal leukoplakia because the definition of FICE was higher than that of WLI. We tried to elucidate the necessity of LCE in patients with esophageal leukoplakia or pale areas. MATERIALS AND METHODS ===================== From May to August 2017, all general patients at our endoscopic center who fulfilled our inclusion criteria were enrolled for screening. All gave their informed consent. Endoscopic screening was performed with a single channel gastroscope (EG450; Fujifilm Co, Tokyo, Japan). The esophageal mucosa of each patient was initially studied with WLI and FICE sequentially during endoscopic insertion. The wavelengths of FICE were set as follows: Red, 550 nm (2); Green, 500 nm (2); Blue, 470 nm (3). During withdrawal, 20 to 40 mL of 1.5% iodine solution was sprayed onto the esophageal mucosa until it was evenly stained. The esophagus was divided into 3 segments---upper, middle, and lower---according to 2 landmarks 24 and 32 cm from the incisors. Endoscopic images of each lesion were captured 2 to 3 minutes after iodine staining. The number and location of esophageal leukoplakia and pale areas, abnormal staining regions in each segment, were immediately recorded by an assistant. Biopsies with clear margins were obtained from unstained regions. All biopsies were sent for pathologic diagnosis. The pathologist was blinded to the endoscopic results. Inclusion Criteria ------------------ Age range from 40 to 80 years.No melena, hematemesis, or shock.No cardiac, pulmonary, hepatic, or renal dysfunction.No coagulopathy.No female patients who were pregnant or preparing for pregnancy.No allergy to iodine. We compared the following items in the esophageal leukoplakia-positive and leukoplakia-negative groups and in the pale area--positive and pale area--negative groups:Common conditions.Cases with abnormal staining regions.Total number of abnormal staining regions in each patient.Total biopsies in each patient.Cases of dysplasia or early-stage cancer. Statistical Analyses -------------------- The statistical analyses were performed using the SPSS 22.0 software package (SPSS, Chicago, IL). Comparisons between groups were performed using Student's *t* test or the *χ*^2^ test. Total areas of abnormal staining and total biopsies in each patient were analyzed using the Mann-Whitney test. The sensitivity, specificity, and area under the receiver operating characteristic curve were used to assess the accuracy of classification. RESULTS ======= A total of 201 patients were enrolled in the study. Table [1](#T1){ref-type="table"} showed demographic and histology data of the 201 patients and their WLI and FICE results. ###### Demographic and Histology Data of the 201 Patients and their WLI and FICE Results ![](mcg-53-e400-g001) Table [2](#T2){ref-type="table"} showed distribution of esophageal leukoplakia, pale areas, dysplasia, and ESCC in the esophagus. ###### Distribution of Esophageal Leukoplakia, Pale Areas, Dysplasia, and ESCC in the Esophagus ![](mcg-53-e400-g002) Both esophageal leukoplakia and pale areas were more frequently detected in middle segment of esophagus. Esophageal leukoplakia in 68 patients and pale areas in 73 patients were distributed in ≥2 segments. Dysplasia of different grades and early-stage ESCC were most frequently found in the middle segment of the esophagus. The average age of patients with dysplasia or ESCC was greater than that of patients without dysplasia or ESCC (61.06±7.779 y vs. 59.58±10.194 y, *P*=0.004). There were no gender difference between patients with or without dysplasia or ESCC (37:35 vs. 54:75, *P*=0.237). Figures [1](#F1){ref-type="fig"}--[3](#F3){ref-type="fig"} showed esophageal leukoplakia via WLI in the lower segment of the esophagus, pale area via FICE, and dark brown area via LCE in the same position, respectively. ![Esophageal leukoplakia via white-light endoscopy in the lower segment of the esophagus (see white solid arrow).](mcg-53-e400-g003){#F1} ![Pale area via FICE in the same position (see white solid arrows).](mcg-53-e400-g004){#F2} ![Dark brown area via Lugol's chromoendoscopy in part of the same position (see white solid arrow); 2 understained regions and 1 unstained region can be detected close to the dark brown area. Pathologic diagnosis of biopsy from the unstained region (see white dotted arrow) showed moderate dysplasia.](mcg-53-e400-g005){#F3} Table [3](#T3){ref-type="table"} showed the differences in groups with or without esophageal leukoplakia, or in groups with or without pale areas. ###### Differences in Groups With or Without Esophageal Leukoplakia, or in Groups With or Without Pale Areas ![](mcg-53-e400-g006) Areas of abnormal staining in the esophageal leukoplakia-positive group were significantly more numerous than those in the esophageal leukoplakia-negative group (*Z*=7.289, *P*=0.000); biopsied areas in the esophageal leukoplakia-positive group were significantly more numerous than those in the esophageal leukoplakia-negative group (*Z*=7.463, *P*=0.000). Areas of abnormal staining in the pale area--positive group were significantly more numerous than those in the pale area--negative group (*Z*=12.127, *P*=0.000); biopsied areas in the pale area--positive group were significantly more numerous than those in the pale area--negative group (*Z*=9.558, *P*=0.000). Figure [4](#F4){ref-type="fig"} showed receiver operating characteristic curves of esophageal leukoplakia and pale area for the detection of dysplasia and early-stage ESCC. ![Receiver operating characteristic (ROC) curves of esophageal leukoplakia and pale area for the detection of dysplasia and early-stage esophageal squamous cell carcinoma. EL indicates esophageal leukoplakia; PA, pale area.](mcg-53-e400-g007){#F4} The sensitivity of esophageal leukoplakia for the detection of dysplasia and early-stage ESCC was 70.0% (35 and 50) with a specificity of 78.8%; the sensitivity of pale area for the detection of dysplasia and early-stage ESCC was 76.0% (38 and 50) with a specificity of 75.5%. DISCUSSION ========== Esophageal cancer is the fourth most frequently diagnosed cancer and the fourth leading cause of death from cancer in China.[@R11],[@R12] Endoscopy is the gold standard for the diagnosis of precancerous squamous lesions. Early detection of ESCC and precancerous lesions is directly related to an improved prognosis. Therefore, a major target of endoscopic screening is to identify these lesions, resect them endoscopically, and/or review them regularly. Unfortunately the early lesions are asymptomatic, and changes in the mucosa are subtle, so that these conditions can easily go unnoticed during a standard endoscopic examination. As a result, it has been suggested that chromoendoscopy techniques could improve diagnostic outcomes. The simplest and most effective way of detecting squamous dysplasia is via LCE.[@R13]--[@R15] It can delineate the margin and significantly improve the endoscopic detection of precancerous or cancerous squamous lesions. The sensitivity and specificity of WLI for the detection of high-grade dysplasia and cancer are 62% and 79%, respectively, compared with the use of LCE, which has a much higher sensitivity of 96% at the expense of a slight loss of specificity of 63%, when using LCE.[@R7] Sometimes endoscopists are reluctant to perform LCE because of patient discomfort. A low concentration of iodine can reduce the severity of esophagitis and increase patient compliance. Application of sodium thiosulfate solution can also reduce the adverse effects of LCE and accelerate color fading by reduction of the iodine. Immediately after spraying of the iodine solution, normal mucosa turned brown, whereas the abnormal mucosa suggestive of dysplasia or cancer turned yellow. Within 2 to 3 minutes, some of the yellow areas changed to pink, which was defined as the "pink-color sign," or positive.[@R16] "Pink-color sign" is an important indication of high-grade dysplasia or cancer, however, this change in color may not appear with mild or moderate dysplasia. One study showed that esophageal squamous dysplasia seems to progress over months to many years depending on the grade. Among those in a high-risk Chinese population, untreated patients with biopsy-proven mild, moderate, and severe squamous dysplasia who were followed endoscopically, 5%, 27%, and 65%, respectively, developed clinically diagnosed ESCC after 3.5 years, and 24%, 50%, and 74% did so after 13.5 years, respectively. Another reported follow-up of patients with moderate or severe dysplasia showed that 22% with moderate dysplasia and 60% with severe dysplasia showed endoscopic (size) or histologic progression during the follow-up period.[@R17]--[@R19] Therefore, based on the high cumulative incidence, it is probable that severe dysplasia requires prompt treatment, moderate dysplasia requires treatment or periodic endoscopic follow-up, and mild dysplasia can be followed over longer intervals. It is known that a significant proportion (up to 62%) of oral squamous cell carcinomas arise from precursor oral potential malignant lesions, such as leukoplakia.[@R8],[@R20] Esophageal leukoplakia are also associated with esophageal cancer. In our experience, esophageal leukoplakia can be classified histologically as nondysplastic or dysplastic, including squamous hyperplasia, chronic inflammation, papillary epithelioma, eosinophilic esophagitis, and squamous dysplasia and early cancer squamous. Squamous hyperplasia is one of the most common benign types and present as "dark brown area" during LCE. The same as ESCC, esophageal leukoplakia, or pale areas, are more often detected in the middle segment of the esophagus. Frequently, esophageal cancer or precancerous lesions occurred close to or in the "dark brown area" in our endoscopic examination. Esophageal leukoplakia and pale areas can serve as markers for a field defect where unstained lesions are more common. FICE digitally limits the wavelength range of the light and offers images with bright color and high light quality. Meanwhile, FICE can be activated during endoscopic screening without the need to interrupt the process.[@R21] Pale areas, which have clear margins and bright colors, can be easily detected in the spot of esophageal leukoplakia with adequate wavelengths of FICE. In our research, we found pale areas are more sensitive than esophageal leukoplakia in predicting precancerous squamous lesions. Thus, FICE may have some advantages in screening ESCC. Our study has some limitations. First, it is a research from a single endoscopic center in China. Second, it is not based on a crossover design. Nevertheless we can draw 2 definite conclusions: esophageal leukoplakia or pale areas are associated with precancerous squamous lesions and ESCC. At least in a high-risk population, LCE should be performed when pale areas are detected via FICE, or esophageal leukoplakia are detected via WLI. The authors would like to thank LetPub (<http://www.letpub.com>) for providing linguistic assistance during the preparation of this manuscript. Y.L., C.Y., and Y.S. contributed equally. The research were supported by Key clinical project of Peking University Third Hospital, No Y73480-03, and special fund project for the development of human resources in Tibet Autonomous region, No 20. Key Laboratory for Helicobacter pylori Infection and Upper Gastrointestinal Diseases in Beijing, No. BZ0371. The study follows the Helsinki Declaration. The authors declare that they have nothing to disclose.
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Infant sleep problems are some of the most common concerns reported by parents of young children. Ask any new parent and most will complain about lack of sleep. Many will also be worried that what they are experiencing isn’t “normal” and that they believe that their child has a problem that needs fixing. So they search books, ask friends and family or even their doctor about what to do about their child’s problematic sleep patterns. And to top it off, they feel immense anxiety and worry about it. Part of this epidemic of parental angst about children’s sleep is that we live in a culture in which parents are repeated told that they need to worry about their child’s sleep, that there will be dire consequences if their child doesn’t get enough sleep. Another problem is that most new parents, having had little experience with children prior to having their own, have little awareness about what truly is “normal” when it comes to infant sleep. Simply being made aware of normal sleep patterns can help alleviate the stress and anxiety parents feel, leading to happier times for the entire family. So what is normal? In this series of posts, we’ll tackle some of the more common sleep concerns parents have with the hope that they can see them as normal, developmental stages for their child. PART 1: THE CRITICAL ROLES OF FEEDING METHOD AND CHANGES IN DEVELOPMENT “My child wakes every hour, all day and night, to feed” Whether it’s every hour, or every two hours, or even three, parents are often concerned when their young infant is waking regularly for feedings. This concern is not surprising given the focus on “sleeping through the night” that our culture pushes. But sleeping through the night is not biologically normal, especially for a breastfeeding baby. At the time of birth, a baby’s stomach can only hold a teaspoon’s worth of milk, meaning that he or she will need to feed frequently to meet the many demands for energy that accompany this period of growth. Although the stomach grows relatively quickly, the fat and protein content in human breastmilk is much lower than in the milk of other mammals and thus infants are required to feed often, resulting in greater night wakings (Ball, 2003; Ball, 2009). Human breastmilk, being designed for infants who need to feed on cue day and night, is easily and quickly digested. Formula, however, is typically made from the breastmilk of another species – cows – and is higher in fat while also containing myriad additives which make it more difficult, and thus slower, to digest. This can affect infant sleep, resulting in unnaturally deeper infant sleep (more time spent in stage 3-4) (Butte, Jensen, Moon, Glaze, & Frost Jr., 1992), a stage of sleep for which it is most difficult to arouse to terminate breathing pauses (especially for arousal deficient infants), therein potentially diminishing the infants capacity to maintain sufficient oxygen. Even so, formula use does not necessarily providing parents with more sleep overall (Doan, Gardiner, Gay, & Lee, 2007). Infants whose primary source of energy is breastmilk will often wake frequently to nurse, something that is essential for the breastfeeding relationship to continue (Ball, 2009). However, regardless of feeding status, many infants wake regularly during the night (Weinraub, Bender, Friedman, Susman, Knoke, Bradley, et al., 2012). Waking through the night is normal and biologically adaptive. In fact, though it is often reported that sleep patterns consolidate in the second year, the pattern differs in breastfed children. Breastfeeding moms may wake more often, but report greater total sleep. For example in a study following breastfed children for 2 years, it was found that these children continue to wake frequently throughout the second year of life, a pattern more in line with cultures in which co-sleeping and full-term (aka “extended”) breastfeeding are more common (Elias, Nicolson, Bora, & Johnston, 1986). Night wakings serve to protect the infant. Night wakings have been reported as being more common in infants who bedshare with a parent, yet the wakings and bedsharing (when done safely) may actually protect the infant from SIDS (Mosko, Richard, & McKenna, 1997; Mosko, Richard, McKenna, & Drummond, 1996). The critical period for SIDS is up to 8 months of age (with the peak at 2-3 months) and night wakings may serve as a protective mechanism. In fact, if we look at parenting historically and cross-culturally, frequent night-wakings coupled with co-sleeping and breastfeeding is the norm for which we should be comparing other infant sleep behaviours. “My child was sleeping through the night and suddenly it’s stopped.” Imagine you’ve been waking regularly with night feeds and arousals, but as time passes they are decreasing. Then you realize you’re now sleeping in nice, long chunks. Hours of sleep all at once! And it’s wonderful. Then suddenly, as quickly as it came, it’s gone. Your wonderful, sleeping-through-the-night child is suddenly waking again. This experience, which is a reality for many, can cause frustration and despair accompanied by the feeling that you’ve done something wrong, or that you must do something get their uninterrupted sleep back again. But here’s the thing: You didn’t do anything. A return to night waking after periods of sleeping through the night is entirely normal. Many children’s sleep will cycle like this for a while. In fact, researchers looking at sleep patterns have found that often between 6 and 12 months, infants who had previously been sleeping long stretches suddenly start to wake more frequently at night (Scher, 1991; Scher, 2001). In fact, in one long-term study looking at child sleep between 3 and 42 months found that there was no stability in night wakings or even sleep duration during this time (Scher, Epstein, & Tirosh, 2004). What causes the change in sleeping pattern? There are likely a variety of reasons, unique to each child. For some, it may be a growth spurt or teething. For others, it may be a cognitive leap that has them buzzing more so than usual or the appearance of separation anxiety. Just recently a study reported that babies tend to wake more often when they are learning to crawl. And for some, we may never know the actual reason. But as children age and each develops a circadian rhythm, they will go through cycles of sleep – some more convenient for parents than others. Parents need to be aware that these changes are entirely normal, even though they can be frustrating. Hopefully once you know that changes are to be expected, you can be better prepared or at least not add anxiety to the sleep disruptions you are forced to deal with once again. Click here to read part two which focuses on the role of individual sleep patterns in infant sleep and why we need not worry when our child doesn’t fit what most other children are doing with respect to sleep. I always tell people- my husband wakes up several times a night to get a snack and I wake up at least once or twice to go to the bathroom, why in the world would we expect our tiny infant to sleep “better” than we do? […] your baby cry or subject them to sleep training, I strongly ask you to do your homework on what normal infant sleep looks like, how it develops and what you can do besides sleep training to get through this time in […] […] real. Let’s be honest and let’s give new parents the very best chance to set themselves up with realistic expectations for the early time in their child’s life where they will be needed just as much at night as they […]
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This invention pertains to a vacuum operated insect collection and viewing device. In particular, the arrangement of the invention is designed to make it easy for children and others having an interest to explore their natural curiosity about insects, without touching or killing them and with comparative safety from being bitten or stung by them. The prior art has many examples of devices which develop a vacuum for the purpose of trapping, collecting and disposing of insects. Insects such as flies, mosquitoes, beetles, spiders have long been considered pests and marked for destruction. Flying insects are considered a particular nuisance, especially when present in the home, dining or food handling establishments. For many years it has been commonplace to use sprays, fly swatters, fly paper, insecticides and various other remedies to deal with unwanted insects. There are known devices that are operated by a vacuum to capture insects and deposit them in a bag or some other cleanable collection element for later disposal. Such devices normally use an elongated funnel of some sort which is put under a negative pressure, and brought near enough to the insect for the insect to be suctioned into the funnel and then into a bag or other container to be subsequently disposed of at a later time. While some components of the invention are common to arrangements in the prior art, the purpose of the invention is, in essence, quite distinct from the purpose of the aforementioned prior art devices. The object of the invention is not to kill the insect being captured but rather to afford an opportunity to examine, study and investigate the physical makeup of the insect of interest. In this regard, it has particular utility for those studying insects, and an innate usefulness as a toy or educational device for children who have an natural inclination to capture and observe insects. The invention provides provides just such opportunity to capture insects without harming them. It furthermore provides a means to capture and study insects without touching them and with ease and a high degree of safety from insect bites. Even dangerous stinging insects can be handled and studied using the device with a general avoidance of fear in the process.
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It is particularly preferred to employ Staphylococcal genes and gene products as targets for the development of antibiotics. The Staphylococci make up a medically important genera of microbes. They are known to produce two types of disease, invasive and toxigenic. Invasive infections are characterized generally by abscess formation effecting both skin surfaces and deep tissues. S. aureus is the second leading cause of bacteremia in cancer patients. Osteomyelitis, septic arthritis, septic thrombophlebitis and acute bacterial endocarditis are also relatively common. There are at least three clinical conditions resulting from the toxigenic properties of Staphylococci. The manifestation of these diseases result from the actions of exotoxins as opposed to tissue invasion and bacteremia. These conditions include: Staphylococcal food poisoning, scalded skin syndrome and toxic shock syndrome. The frequency of Staphylococcus aureus infections has risen dramatically in the past 20 years. This has been attributed to the emergence of multiply antibiotic resistant strains and an increasing population of people with weakened immune systems. It is no longer uncommon to isolate Staphylococcus aureus strains which are resistant to some or all of the standard antibiotics. This has created a demand for both new anti-microbial agents and diagnostic tests for this organism. Aromatic amino acids are synthesized in bacteria from the common precursor, chorismic acid. Chorismic acid is itself synthesized in bacteria from phosphoenol pyruvate and erythrose4-phosphate via 3-dehydroquinate which is made by a synthase encoded by the aroB gene. The gene in Escherichia coli has been cloned (see Millar G, Coggins JR FEBS Lett, 200(1):11-17 (1986)). Substantial effort has been invested this century in the successful discovery and development of antibacterials. Paradoxically, although antibacterials are devised to eradicate infection in mammals, we know almost nothing of the physiology of bacterial pathogens in infective situations in the host. Using sequences from the Staphylococcus aureus chromosome, we have developed an RT-PCR based procedure which allows us to identify those bacterial genes transcribed at any stage of infection and also from different niches of infection. The derivation of such information is a critical first step in understanding the global response of the bacterial gene complement to the host environment. From the knowledge of bacterial genes both of known and unknown function which are widely transcribed in the host it is possible to attempt to ascertain by database searching those which are present only in the eubacteria. Further prioritization of such genes by consideration of the likely role of their products towards the maintenance of infection and the facility of setting up a screen for inhibitors of the biochemical function indicated by their homology to characterised genes allows the compilation of a shortlist for gene essentiality studies using genetic deletion or controlled regulation techniques. The proteins expressed by genes shown to be necessary for growth in vitro or in pathogenesis in animal models provide novel targets for antibacterial screening to find agents which are broadly inhibitory towards pathogenesis. This invention provides S. aureus WCUH 29 polynucleotides which are transcribed in infected tissue, in particular in both acute and chronic infections. Clearly, there is a need for factors, such as the novel compounds of the invention, that have a present benefit of being useful to screen compounds for antibiotic activity. Such factors are also useful to determine their role in pathogenesis of infection, dysfunction and disease. There is also a need for identification and characterization of such factors and their antagonists and agonists which can play a role in preventing, ameliorating or correcting infections, dysfunctions or diseases. The polypeptides of the invention have amino acid sequence homology to a known 3-dehydroxyquinate synthase (EC 4.6.1.3) protein, identified as AROB BACSU in the Swiss Prot database. See Swiss Prot, Accession Number P31102.
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Imagine a barking dog, a furry spider or another perceived threat and your brain and body respond much like they would if you experienced the real thing. Imagine it repeatedly in a safe environment and soon your phobia—and your brain’s response to it—begins to subside. That’s the takeaway of a new brain imaging study led by CU Boulder and Icahn School of Medicine researchers, suggesting that imagination can be a powerful tool in helping people with fear and anxiety-related disorders overcome them. “This research confirms that imagination is a neurological reality that can impact our brains and bodies in ways that matter for our wellbeing,” said Tor Wager, director of the Cognitive and Affective Neuroscience Laboratory at CU Boulder and co-senior author of the paper, published in the journal Neuron. About one in three people in the United States have anxiety disorders, including phobias, and 8 percent have post-traumatic stress disorder. Since the 1950s, clinicians have used “exposure therapy” as a first-line treatment, asking patients to face their fears—real or imagined—in a safe, controlled setting. Anecdotally, results have been positive. But until now, very little has been known about how such methods impact the brain or how imagination neurologically compares to real-life exposure. “These novel findings bridge a long-standing gap between clinical practice and cognitive neuroscience,” said lead author Marianne Cumella Reddan, a graduate student in the Department of Psychology and Neuroscience at CU Boulder. “This is the first neuroscience study to show that imagining a threat can actually alter the way it is represented in the brain.” Measuring the minds-eye Functional magnetic resonance imaging (fMRI) is used to measure brain activity. For the study, 68 healthy participants were trained to associate a sound with an uncomfortable, but not painful, electric shock. Then, they were divided into three groups and either exposed to the same threatening sound, asked to “play the sound in their head,” or asked to imagine pleasant bird and rain sounds—all without experiencing further shocks. The researchers measured brain activity using functional magnetic resonance imaging (fMRI). Sensors on the skin measured how the body responded. In the groups that imagined and heard the threatening sounds, brain activity was remarkably similar, with the auditory cortex (which processes sound), the nucleus accumbens (which is associated with reward learning) and the ventromedial prefrontal cortex (associated with risk and aversion) all lighting up. After repeated exposure without the accompanying shock, the subjects in both the real and imagined threat groups experienced what is known as “extinction,” where the formerly fear-inducing stimulus no longer ignited a fear response. Essentially, the brain had unlearned to be afraid. “Statistically, real and imagined exposure to the threat were not different at the whole brain level, and imagination worked just as well,” said Reddan. Notably, the group that imagined birds and rain sounds showed different brain reactions, and their fear response to the sound persisted. “I think a lot of people assume that the way to reduce fear or negative emotion is to imagine something good. In fact, what might be more effective is exactly the opposite: imagining the threat, but without the negative consequences,” said Wager. Unlearning fear Previous research has shown that imagining an act can activate and strengthen regions of the brain involved in its real-life execution, improving performance. For instance, imagining playing piano can boost neuronal connections in regions related to the fingers. Research also shows it’s possible to update our memories, inserting new details. The new study suggests that imagination may be a more powerful tool than previously believed for updating those memories. Marianne Reddan (Credit: Ernest Mross) “If you have a memory that is no longer useful for you or is crippling you, you can use imagination to tap into it, change it and re-consolidate it, updating the way you think about and experience something,” said Reddan, stressing that something as simple as imagining a single tone tapped into a complex network of brain circuits. She notes that there was much more variance in brain activity in the group that imagined the tone versus the ones who really heard it, suggesting that those with a more vivid imagination may experience greater brain changes when simulating something in their mind’s eye. As imagination becomes a more common tool among clinicians, more research is necessary, they write. For now, Wager advises, pay attention to what you imagine. “Manage your imagination and what you permit yourself to imagine. You can use imagination constructively to shape what your brain learns from experience.” Or, as writer and philosopher Mary Baker Eddy put it, “Stand porter at the door of thought.”
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Content-addressed memories, sometimes known as associative memories, are well known in the prior art. Whereas conventional location-addressable memory is designed to retrieve data from a specific address, a content-addressable memory system finds and retrieves a collection of closely related data, called a record, by comparing a keyword value known to be associated with or located within the desired data with the data stored in the content-addressed memory. Once a match is found, the rest of the record can be accessed. Thus, all records containing one or more of the keyword values will be found without any prior knowledge of where the records are stored. Whereas any memory is searchable for keyword values by sequentially reading and matching the words in the memory with the keyword value, the records of a content-addressed memory are searched simultaneously and in parallel for a match. The word cells are arranged in parallel and share a common data bus so that the keyword value can be sent simultaneously to all the word cells. The speed with which a content-addressed memory finds all records matching a keyword value is, consequently, significantly faster. For example, if a court's written opinion is a record of the content-addressed memory, it may be found by searching for the names of the parties in the suit. The names of the parties are the keyword values. The name of a party in this example is always stored in a particular area of the record, called a field or subfield; the name of the case is the value. Thus, a keyword value defines a particular field or subfield and a particular value. Only a particular area of all records stored in the content-addressed memories need, therefore, be searched and compared with a particular keyword value. Several keyword values, called keyword value combinations, may also be used to find the desired record or records. A typical application of a content-addressable memory is a cache memory. Instead of having to retrieve data stored in a large main memory, frequently used data is stored in a smaller content-addressable memory, thus permitting quicker retrieval. Each word cell contains a record and a corresponding address in the main memory. With this address as a keyword value, the record is retrievable from the cache memory by asking it, in effect, for the record having that address, no matter where it is actually stored within the memory. In storing and quickly retrieving large amounts of data, prior art content-addressed memories are presented with several physical limitations. In order to store large records, either the word cells need to be made very large, or the record must be stored in a separate "numbered-cell" storage where the keyword value is mapped to the address of the "numbered cell." The disadvantage of the first technique is that the size of the word cells are fixed and large, at least large enough to accommodate all the necessary values of its foreseeable use. Content-addressed memories, thus, must either be individually tailored to specific uses, making high-volume production techniques unavailable to reduce costs, or there will be wasted storage space. The numbered-cell technique, on the other hand, taxes the speed of the memory when more than one keyword value is used to retrieve a record. Instead of storing the entire record in the content-addressed memory, it is stored in a "numbered cell" memory, with the number, or address, of the cell stored in the content-addressed memory, along with a few selected keyword values. Once a match is made, the number, or address, of the record is read, and the record of interest is accessed. After a list of records satisfying a first keyword value is found, however, the records on the list are matched sequentially with other keyword values to find desired subsets of the matched records, since each record must be individually read and matched from the main memory. A significant time penalty is, thus, imposed for matching combinations of keyword values. There is a need, therefore, for a content-addressed memory that permits the flexibility of storing records of any desired size and quickly accessing the records with keyword value combinations.
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APT Basilicata APT Basilicata Basilicata turistica History The very ancient land known as Basilicata was already inhabited in the prehistoric age. The settlements of Venosa and the Bradano Valley date from the Paleolithic period while the organized agricultural villages around Matera and Melfi sprang up during the Neolithic period. From that time until the Bronze Age the region became an important centre of communication between the Jonian and Tyrrhenian populations, giving rise to important settlements. The inland regions began to be populated during the Iron Age. It was during this phase that many Indo-Europeans arrived in Lucania, among whom the Liky from the Illyrian coast. In the 8th century B.C. Greek colonies landed on the Lucanian shores of the Jonian Sea. This historic event gave birth to that flowering civilization that will be remembered in history as the Magna Graecia. Metaponto, Siris and Heraclea are the most important settlements. Between the 6th century and the 5th century B.C. certain Osco-Sabellic tribes came down from the Irpinia, while the Lucanians settled the more inland regions. Later, in the 5th and 4th centuries B.C., the Lucanians attacked the Greek colonies along the Jonian coast in their quest for new land to cultivate. Meanwhile, between the 4th century and 3rd century B.C., the Romans pushed their way into Lucania as they continued their expansion. At first the Lucanians were allied with the Romans against the Samnites. Later, not wanting to yield to Roman domination, they allied themselves with the Samnites and the Greek colony in Taranto to combat the Romans. Meanwhile, in 291 B.C., Venusia (today Venosa) becomes the first Roman colony in Lucanian territory. The Romans fight against Pyrrhus who was rushing to the aid of the Greek colonies, and loose a battle that took place between the areas of Metaponto and Heraclea (today Policoro), which became famous for the heavy losses incurred on both sides. In the northeast, Roman domination increases: the town of Grumentum (today Grumento) is founded and the road that connects Grumentum to Venusia is constructed (Via Herculia). 280 B.C. witnesses the end of Magna Graecia. In the 2nd century B.C. Lucania is under Roman domination. The proud and warlike Lucanians rebel against Rome, which had decided to impose landed estates, but are defeated. From 27 B.C. to 14 B.C., under the Augustan Empire, Lucania is divided into two parts and unified with Apulia, the Regio II, and with Brutium, the Regio III. At the end of the 3rd century Dioclesian reunites the area, unifying it with Brutium. With the decline of the Western Roman Empire the region sinks back into deep isolation, which destroys the already impoverished economy. We are in the Middle Ages. Between the 6th century and the 9th century, the Longobards annex Lucania (with the exception of the Byzantine possessions in the region of Matera) to the Duchy of Benevento. The Byzantines, gathered in Lucania in their effort to escape religious persecution in the Orient, give life to the phenomenon of the Rupestrian (rock) Churches. They proliferate on the Murgia of Matera. Meanwhile, the Saracen invasions force the Lucanians to retreat to the surrounding mountains and hills. Between the 8th century and the 9th century, Matera is annexed to the Duchy of Benevento, while the rest of the region passes under Byzantine domination. In the 11th century and 12th century the Normans conquer Lucania, making it the centre of Italian political life. In 1059, Melfi is the capital of the Norman realm. When Norman domination ends, the Swabians and Angevins compete for control of Lucania and southern Italy. Frederick II of Swabia is born. In 1231, in Melfi, he enacts the Constitutiones Utriusque Regni Sicilae (the Constitutions of the Two Sicilies). At the end of the 13th century the Angevins control the Realm of Naples and the Two Sicilies. Feudalism has begun, during which time many Lucanian lordships spring up and which the Aragonese attempt to oppose. The Barons, faithful to the Angevins, try to overthrow the Aragonese Reign and the 'Congiura dei baroni' (baron conspiracy) is planned in the Miglionican Castle in 1441. Between the 13th century and the 16th century Bourbon power consolidates. Certain Albanian communities arrive in Basilicata, settling along the slopes of Vulture and the Pollino Massif. In 1663, Matera is the capital of the Lucanian Province of the Kingdom of Naples. This period witnesses the beginning of bloody rebellions by peasants against the barons who exploit the land, forcing the population into famine. In 1707, the Austro-Sabaudian army occupies Lucania, and after the Treaties of Utrecht and Rastadt it passes into the hands of Charles VI of Austria. The Bourbons return to power with the Peace Treaty of Aquisgrana. In 1799 a peasant rebellion is repressed with mass executions. Then power passes briefly to the French, who after a short time are forced to return it again to the Bourbons. A part of the Lucanian bourgeoisie adheres to the 'Moti carbonari' (Carbonari uprisings). Between 1861 and 1868 the entire region is affected by the phenomenon of Brigantaggio (banditry), rebellions against power generated by the extreme isolation of the population and which finds its ideal habitat in the thick woods of Mount Vulture. The beginning of the 20th century, in 1902, sees the first meeting of Socialists in Potenza. Poverty has reached unacceptable levels and the phenomenon of emigration begins, reaching its high point in 1913. In 1943, Matera is the first southern Italian province to rebel against Nazi-Fascist occupation. When World War II ends, it becomes necessary to tackle the problem of the 'Sassi of Matera' (ancient rock dwellings) which, because of overpopulation, had become a health risk. In 1952, a state law decrees the evacuation of the Sassi district. During the same period 'Riforma Fondiaria' (land reform) begins and transforms the face of the region. Unfortunately, emigration damages the communities of Basilicata since it provokes a progressive demographic impoverishment. The 1980 earthquake in Irpinia creates serious problems in the entire northern region and in the capital Potenza. The University of Basilicata is established in Potenza in 1984, which a few years later opens a campus in Matera. In 1986, the Italian government enacts a law to finance the restoration of the Sassi of Matera, which is still being carried out among a multitude of problems. At the beginning of 1994, UNESCO declares the Sassi of Matera 'heritage of humanity to be handed down to future generations' and counts it among the territories under its protection. FIAT establishes an enormous factory in the industrial zone of S. Nicola of Melfi. In the same year the National Park of Pollino is established.
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Q: Read and print from a text file N lines at a time using a generator only Python 3.6.0 textfile = "f:\\mark\\python\\Alice_in_Wonderland.txt" N = 60 def read_in_lines(file, n): with open(file) as fh: for i in range(n): nlines = fh.readline() if nlines: yield nlines else: break for lines in read_in_lines(textfile, x): print(lines) File is here: https://www.gutenberg.org/files/11/11.txt My goal is to read in this file N lines at a time, then print the lines, then read in the next N lines, print, repeat... If N = 3, output should look like: line1 line2 line3 line4 line5 line6 line7 line8 line9 line10 <-- assumes this is the last line in the file The above print pattern should hold for any value of 'N'. If 'N' = 4: line1 line2 line3 line4 line5 line6 line7 line8 etc. You get the idea. NO lists. No built in functions (islice, etc.). I need to use a generator only. Each iteration must contain a string containing up to the number of lines specified by 'N'. Two issues: 1) The above code returns 'N' lines, then stops. I assume I need to put the whole thing in a loop, but I am unsure of how to proceed. (Newbie...) 2) The file contains A LOT of blank lines. Every single time I try to use strip() or any of it's variants, regardless of how big I make 'N' it only ever prints one line. nlines = fh.readline().strip <-- adding in .strip() With N = 6000 I get: Project Gutenberg's Alice's Adventures in Wonderland, by Lewis Carroll Process finished with exit code 0 If I get rid of .strip() I get all the lines but not in the format I want. I am on a Win 10 machine. In Notepad++ all of the end of file symbols are CRLF. A: Solved: textfile = "f:\\mark\\python\\test.txt" def read_n(file, x): with open(file, mode='r') as fh: while True: data = ''.join(fh.readline() for _ in range(x)) if not data: break yield data print() for nlines in read_n(textfile, 5): print(nlines.rstrip()) Output: abc 123 def 456 ghi 789 jkl abc 123 def 456 ghi 789 jkl abc 123 def 456 ghi 789 jkl abc 123 def 456 ghi 789 jkl
3
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According to conventional practice, joints in lead anodes used in the mining industry are formed using traditional lead burning procedures (e.g., torch welding) in which lead is melted by hand to form the welds or joints. There are, however, a number of disadvantages associated with conventional lead burning procedures as will be discussed below. Conventional lead burning procedures involve a high degree of risk to the worker. First, the heat generated during creation of the weld can result in worker injury. Second, during melting of the lead, the ambient levels of lead can rise to toxic levels. If inhaled, it could lead to lead poisoning, one of the oldest forms of occupational hazards. As a result, a variety of bodily processes are affected, as well as the deterioration of numerous organs such as the heart, bones, intestines, kidneys, and reproductive and nervous systems. Conventional lead burning procedures often produce anodes having defective welds which have repeatedly lead to product failure. By training and using a specially skilled work force, the potential for defective welds can be reduced, but is not eliminated, as incomplete welds can occur despite use of skilled workers. In these incomplete welds, the joint visually appears sound. However, the two melt pools created to form the weld have never merged, thereby greatly reducing the material available in the anode joint for current transport and creep (i.e., deformation) resistance. Even when an anode having a defect-free joint is created, conventional lead burning procedures create an undesirable heat affected zone in the base metal structure around the region of the anode joint. In this heat affected region, the grain structure of the materials in the anode is altered by the heat used to create the joint. The altered grain structure can be a further source of reduced corrosion resistance and decreased creep resistance. Moreover, lead and copper (used to create anodes) do not naturally weld together. As such, various techniques, such as soldering, are utilized in conventional lead burning procedures to join the lead and copper, thereby constructing the anode. Therefore, in addition to the foregoing disadvantages, conventional anode manufacturing processes are more costly due to the increased manufacturing time and materials involved in joining the lead and copper. Accordingly, since conventional lead burning techniques used to produce anodes are rife with problems, companies must devote costly resources to safety, worker training, quality control testing, and manufacturing. To date, conventional lead burning techniques have failed to adequately address these issues in the anode industry. In view of the foregoing, there is a need in the art for an anode manufacturing technique which greatly reduces or eliminates the disadvantages of the prior art.
3.65625
4
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We learned about place value. We made "No Davids" after reading the book to learn about school rules. We talked about Character Traits. We played Homeworkopoly for turning in our homework for the week. We played the place value game after learning about place value, the value of a digit, expanded notation and the word form. We are now learning how to rename a number. The first week we learned about story elements (characters, setting and plot) and the beginning, middle and end. By Ellie and Aryanna
3.046875
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Evolution from primordial oligomeric repeats to modern coding sequences. It seems as though nature was most innovative at the very beginning of life on this Earth a few billion years ago. For example, the functional competence of most, if not all, of the sugar-metabolizing enzymes was clearly established before the division of eukaryotes from prokaryotes eons ago, each critical active-site amino acid sequence being conserved ever since by bacteria as well as by mammals. I contend that this initial innovativeness was due to the first set of coding sequences being repeats of base oligomers, thus encoding polypeptide chains of various periodicities; such periodical polypeptide chains can easily acquire alpha-helical and beta-sheet-forming segments. In fact, the entire length of sugar-metabolizing enzymes is comprised of alternating alpha-helical and beta-sheet-forming segments. In the prebiotic (therefore nonenzymatic) replication of nucleic acids, what was in short supply was long templates, for there apparently was no inherent obstacle in copying of long templates, if such existed, in the presence of Zn2+. I submit that in this prebiotic condition, only those nucleotide oligomers that were internal doubles were automatically assured of progressive elongation to become long templates. For example, a decamer that was a pentameric repeat and its complementary sequence may pair unequally to initiate the next round of replication: first unit pairing with second, and a paired segment serving as a primer. As a consequence of this unequal pairing, decameric templates managed to become pentadecameric templates only after one round of replication, and this elongation process had no inherent limit.
3.109375
3
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Currently, wireless communications systems find application in many contexts involving the transfer of information from one point to another, and there exists a wide range of modalities suited to meet the particular needs of each. These systems include cellular telephones and two-way radios for distant voice communications, as well as shorter-range data networks for computer systems, among many others. Generally, wireless communications involve a radio frequency (RF) carrier signal that is modulated to represent data and the modulation, transmission, receipt and demodulation of the signal conforming to a set of standards. For wireless data networks, example standards include Wireless LAN (IEEE 802.11), BLUETOOTH® (IEEE 802.15.1), and ZIGBEE® (IEEE 802.15.4), which are generally time domain duplex systems where a bidirectional link is emulated on a time divided communications channel. A fundamental component of a wireless communications system is the transceiver which includes the transmitter and receiver circuitry. The transceiver, with its digital baseband subsystem, encodes the digital data to a baseband signal and modulates the baseband signal with an RF carrier signal. The modulation utilized for WLAN includes orthogonal frequency division multiplexing (OFDM), quadrature phase shift keying (QPSK) and quadrature amplitude modulation (16 QAM, 64 QAM); for WLAN includes GFSK and 4/8-DQPSK; and for Zigbee includes BPSK and OQPSK (or MSK). Upon receipt of the signal from the antenna, the transceiver downconverts the RF signal, demodulates the baseband signal and decodes the digital data represented by the baseband signal. The antenna connected to the transceiver converts the electrical signal to electromagnetic waves, and vice versa. Depending upon the particular configuration, the transceiver may include a dedicated transmit (TX) line and a dedicated receive (RX) line or the transceiver may have a combined transmit/receive line. In the case of separate TX and RX lines, the transmit line and the receive line are typically tied to a single antenna, particularly for low-cost and/or small-size applications. The circuitry between the transceiver and the antenna is commonly referred to as the front end module (FEM). The FEM includes an RF power amplifier (PA) which generates output transmit signals by amplifying weaker input signals in wireless devices, such as cellular telephone handsets. Many of these communication devices are configured to operate in different frequency bands for different communication systems. For example, third generation (3G) cellular communication systems, 4G cellular (LTE) systems, 802.11 WLAN systems, etc. It is thus desirable to have a front end module capable of meeting the performance requirements of modern wireless standards such as 802.11, 3G and 4G cellular systems while reducing manufacturing complexities, size and cost.
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Measurements taken by ESO’s New Technology Telescope combined with a model of asteroid Itokawa's surface topography reveal that different parts of this asteroid have different densities. The shape model used for this view is based on the images collected by JAXA's Hayabusa spacecraft. Image released The innards of an asteroid have been measured for the first time. Scientists using a European Southern Observatory telescope have made precise measurements of Asteroid Itokawa's density. They discovered that different parts of the asteroid have different densities, giving the scientists clues about the asteroid's formation in the solar system. The researchers explain the strangely shaped asteroid Itokawa in a new video. Itokawa is a stony composite asteroid. The peanut-shaped space rock is about 1,755 feet (535 meters) long on its longest side and takes about 556 days to orbit the sun. Scientists measured the density by studying images of Itokawa taken by the New Technology Telescope at the La Silla Observatory in Chile, as well as by other telescopes, from 2001 to 2013. Stephen Lowry, a researcher at the University of Kent, and his team measured how the brightness of the space rock varies during its rotation, ESO officials said. [See more photos of asteroid Itokawa] This very detailed view shows the strange peanut-shaped asteroid Itokawa. This picture comes from the Japanese spacecraft Hayabusa during its close approach in 2005. Image released Feb. 5, 2014. (Image credit: JAXA) "This is the first time we have ever been able to determine what it is like inside an asteroid," Lowry said in a statement. "We can see that Itokawa has a highly varied structure — this finding is a significant step forward in our understanding of rocky bodies in the solar system." By looking at the change in Itokawa's brightness over time, the researchers tracked how the asteroid's spin period changed over time. By understanding that information plus its shape, the astronomers could also map the asteroid's interior density, ESO officials said. Lowry and his colleagues found that sunlight was actually affecting the way the asteroid spins. Thanks to some very precise measurements, the team found that Itokawa's rotation period changes by 0.045 seconds per year, ESO officials said. While this may seem like a miniscule amount, it's something that can only happen if the two halves of the peanut-shaped space rock have different densities. This very detailed view shows the strange peanut-shaped asteroid Itokawa. This picture comes from the Japanese spacecraft Hayabusa during its close approach in 2005. Image released Feb. 5, 2014. (Image credit: JAXA) Until now, scientists had estimated asteroid interior properties through overall density measurements, ESO officials said. Now that they know the internal structure of an asteroid can vary, scientists can try to work backward to see how the space rock formed. Scientists now think it's possible that two parts of a double asteroid crashed together and merged to create Itokawa, ESO officials said, although no one is sure exactly how it formed. "Finding that asteroids don't have homogeneous interiors has far-reaching implications, particularly for models of binary asteroid formation," Lowry said in a statement. "It could also help with work on reducing the danger of asteroid collisions with Earth, or with plans for future trips to these rocky bodies.” This very detailed view shows the strange peanut-shaped asteroid Itokawa. This picture comes from the Japanese spacecraft Hayabusa during its close approach in 2005. Image released Feb. 5, 2014. (Image credit: JAXA) Japan's Hayabusa spacecraft collected tiny dust grains from Itokawa in 2005 during a 1.25 billion-mile (2 billion kilometers) mission that took seven years to complete. The probe returned to Earth with the space rock samples in 2010. The unmanned Hayabusa arrived at Itokawa when the asteroid was about 180 million miles (290 million km) from Earth. Scientists in Japan are also considering a follow-up to the Hayabusa mission called Hayabusa 2. The new probe would launch to and sample 1999 JU3, a carbonaceous asteroid. Follow Miriam Kramer @mirikramer and Google+. Follow us @Spacedotcom, Facebook and Google+. Original article on Space.com.
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The chemical structure of xanthan is composed of a linear cellulosic (1→4)-β-D-glucose polymer with trisaccharide side chains composed of mannose, glucuronic acid and mannose, attached to alternate glucose residue in the backbone. (Milas and Rinaudo, Carbohydrate Research, 76, 189-196, 1979). Thus xanthan can be described as a branched chain polymer with a pentasaccharide repeat unit; normal xanthan typically has 2000-3000 pentasaccharide repeat units. The xanthan polymer is typically modified by acetylation and pyruvylation of the mannose residues. The fermentation of carbohydrates to produce the biosynthetic water-soluble polysaccharide xanthan gum by the action of Xanthomonas bacteria is well known. The earliest work was conducted by the United States Department of Agriculture and is described in U.S. Pat. No. 3,000,790. Xanthomonas hydrophilic colloid (“xanthan”) is an exocellular heteropolysaccharide. Xanthan is produced by aerobic submerged fermentation of a bacterium of the genus Xanthomonas. The fermentation medium typically contains carbohydrate (such as sugar), trace elements and other nutrients. Once fermentation is complete, the resulting fermentation broth (solution) is typically heat-treated. It is well established that heat treatment of xanthan fermentation broths and solutions leads to a conformational change of native xanthan at or above a transition temperature (TM) to produce a higher viscosity xanthan. Heat treatment also has the beneficial effect of destroying viable microorganisms and undesired enzyme activities in the xanthan. Following heat-treatment, the xanthan is recovered by alcohol precipitation. However, heat treatment of xanthan fermentation broths also has disadvantages, such as thermal degradation of the xanthan. Heating xanthan solutions or broths beyond TM or holding them at temperatures above TM for more than a few seconds leads to thermal degradation of the xanthan. Degradation of xanthan irreversibly reduces its viscosity. Accordingly, heat treatment is an important technique with which to control the quality and consistency of xanthan. Xanthan quality is primarily determined by two viscosity tests: the Low Shear Rate Viscosity (“LSRV”) in tap water solutions and the Sea Water Viscosity (“SWV”) in high salt solutions. Pasteurization of xanthan fermentation broths at temperatures at or above TM has been found to yield xanthan of a higher viscosity as indicated by higher LSRV and SWV values. Xanthan polymer is used in many contexts. Xanthan has a wide variety of industrial applications including use in oil well drilling muds, as a viscosity control additive in secondary recovery of petroleum by water flooding, as a thickener in foods, as a stabilizing agent, and as a emulsifying, suspending and sizing agent (Encyclopedia of Polymer Science and Engineering, 2nd Edition, Editors John Wiley & Sons, 901-918, 1989). Xanthan can also be used in cosmetic preparations, pharmaceutical vehicles and similar compositions. There is a need in the art to produce a xanthan polymer with higher specific viscosity characteristics in the unpasteurized state. Such a higher specific viscosity xanthan polymer could provide more viscosity at equivalent xanthan concentrations, for example, for food, industrial, and oilfield applications.
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1976 Longling earthquake The 1976 Longling earthquake in Yunnan Province, People's Republic of China, was a doublet earthquake, with two main shocks striking just east of Longling at 12:23:20 and 14:00:22 UTC (20:23 and 22:00 local time). The magnitudes were estimated at 6.7 and 6.6, respectively, on the scale, and 6.9 and 7.0 on the scale; Chinese sources put these at 7.4 and 7.3 on the scale. The region is noted for the quantity and intensity of its earthquakes, and the complexity of its tectonics, which are closely related to the collision between the Indian and Eurasian tectonic plates. No one died in the Longling county town Loss in the 9 counties in Baoshan, Lincang and Dehong were 98 deaths, 451 severe injuries and 1991 light injuries. 420,000 buildings collapsed in an area of 1883 square kilometers. Geology Yunnan is a mountainous region lying east of Tibet, and north of the Red River Fault that strikes southeast along the Red River into North Vietnam and the South China Sea. The Red River fault is deep – some believe it may reach the lithosphere – and forms a major tectonic boundary that separates Indochina from the South China block. The seismotectonics of Yunnan and the adjacent areas is driven by the collision of the Indian Plate with the Eurasian Plate. This has uplifted the Tibetan Plateau (and the Himalaya Mountains) and forced it eastwards, pushing the South China Block and Indochina towards the westward subducting Philippine Sea Plate and creating various extensional structures. All of this has created a complicated geological structure with many faults, which in western Yunnan has allowed heat and fluids from the subducting Indian Plate to rise into the upper crust, creating the Tengchong volcanic field to the north of Longling and the Longling fault (location of the first event), and west of the Nu River and Nu River fault (location of the second event). It appears that igneous intrusions have weakened the bedrock in this area, which has led to uneven accumulations of stress, which caused the earthquake. See also 1976 Tangshan earthquake (July 28) 1976 Songpan–Pingwu earthquake (August 16–23) List of earthquakes in 1976 List of earthquakes in China Notes Sources . . . . . . . (in Chinese with English abstract). . External links 1976 Longling Category:1976 in China Category:1976 earthquakes
3.15625
3
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Nicholas Purcell of Loughmoe Nicholas Purcell, 13th Baron of Loughmoe (1651 – 4 March 1722) was the son of James Purcell of Loughmoe and the maternal nephew of James Butler, 1st Duke of Ormonde. A member of the King's Privy Council, Purcell was the right-hand man to Patrick Sarsfield, Earl of Lucan. In 1687 Nicholas Purcell raised a troop of horse to support King James II — they were called the "Yellow Horse," probably on account of the uniform of the men. Nicholas fought at the Battle of the Boyne and at the Battle of Aughrim, and was a signatory to the Treaty of Limerick. He did not flee to Europe after Limerick but remained in Ireland to fight for the rights of Roman Catholics. The Marquis de Ruvigny notes that Nicholas Purcell of Loughmoe was made Baron Loughmore by King James II in 1690. While there is little other evidence to confirm the creation of this peerage, it would enter the ranks of those titles created by the King while in exile . Early years Born sometime in 1651, Nicholas Purcell of Loughmoe Castle was the first son of Colonel James Purcell (1609–1652), 12th Baron of Loughmoe Castle, and Elizabeth Butler, daughter of Thomas Butler, Viscount Thurles, and Elizabeth, Lady Thurles and sister of James Butler, 1st Duke of Ormonde. The May 1652 Act of Settlement saw Nicholas' father, Colonel James Purcell, a Roman Catholic, lose the Tipperary lands the family had held since 1198. The Colonel was set not to be compensated with land in Connaught, however, as his fortunate marriage to the sister of the Duke of Ormonde enabled a powerful contact who ensured the allocation of some property. The allocation of land did not occur without difficulty however. On 13 September 1652, Colonel James Purcell, Baron of Loughmoe died and was buried in the Holy Cross Abbey. Between 1652 and 1656, his widow lost and regained her lands in Galway no fewer than four times . With the Restoration of King Charles II in 1660, the family's fortunes improved. Elizabeth Purcell returned to Loughmoe and again enjoyed the jointure of £300 a year she had received before her removal. The young Baron Nicholas would have been eight or nine at this time and it was probably the first time he had seen his ancestral home. About this time, Elizabeth Purcell married Colonel John Fitzpatrick at Loughmoe; her children were present at the wedding . By King's Order in a letter dated circa 31 October 1661 the Duke of Ormonde, Baron Nicholas' maternal uncle, was appointed guardian of the young Baron. It would appear that the majority of work in respect to the recovery and management of the Baron's estate fell to Colonel Fitzpatrick who discharged his duty with scrupulous fidelity. Under the Down Survey of 1663 all of the historically Purcell lands, a total of were granted to Baron Nicholas. These lands ran from Holy Cross to Templemore, and included the castles of Loughmoe, Rathelty, Dovea, Ballinahow, Lisheentagirt, Beakstown, Brownestown and Rorodstown. The total value of the property in 1640 was £4,340. Again, between 1666 and 1686 little is known of the life of Baron Nicholas. This is a significant period of his life, from age 15 to 35. It is known that Baron Nicholas was tutored privately at Loughmoe and spent a considerable part of their day horse riding. Sometime in this period Baron Nicholas married the Honourable Rose Trevor, daughter of Viscount Dungannon . Military Beginnings With a strong history of loyalty to the Catholic cause, Nicholas Purcell was commissioned Captain on 12 February 1686 in the army enrolled by Lord Tyrconnell to uphold the cause of King James II. In May 1686 he was admitted as a member to the King's Privy Council of Ireland, he was 35. It was at this time in 1686 that King James II confirmed the title of Baron of Loughmoe to Colonel Nicholas. Nicholas Purcell married Ellis Browne sometime around 1688; she was 20 years his junior. Ellis Browne was the daughter of Sir Valentine Browne who had a high command in the army of King James II and was created Baron Castlerosse and Viscount Kenmare by the King. In 1689 Col. Nicholas Purcell represented the County of Tipperary in the Parliament in Dublin. Why he was there we are not certain but on 1 May 1689, accompanying His Majesty King James II from Brest, Col. Nicholas Purcell arrived home to Ireland. At this time Col. Purcell participated in the siege of Derry and an incident there provides an insight into the horsemanship and great courage of Col. Nicholas Purcell. A garrison of William's troops lay entrenched by or near a strand. The garrison fired at the horses of the oncoming Jacobite soldiers and were successful in downing many. Those who did succeed in reaching the defences found themselves confronted by "a dry bank of seven-foot high at the waterside", which most of them quickly decided was impracticable for cavalry. The commanding officer, Edmund Butler, Viscount Mountgarret's second son, "being extraordinarily well mounted", showed the way and spurring his horse, flew over the bank, only to be at once made prisoner. Colonel Nicholas who was close behind Butler, had his horse killed under him and only saved himself by quickly jumping onto the horse's hind and heaving himself backwards. After the Siege of Derry, Colonel Nicholas was sent by the King to join the Highland forces of the "Bonnie Dundee". The London Gazette reported 300 Irish troops and 60 horses were landed in Argyllshire, having been transported there by three French men-of-war and several other vessels from Carrickfergus. Colonel Nicholas had brought with him of powder, ball, match and flint, and was under the command of Major-General Alexander Cannon. On the morning of 17 May 1689, 400 men of Colonel Purcell's regiment landed in small boats at Lochaber and escaped capture by Sir George Rooke by hiding in the mountains of Mull. On 12 July 1689 they landed at Duart in the Isle of Mull. During their short passage the French frigates had captured the Scottish privateer Pelican and her consort after a sharp encounter. Purcell's Dragoon's joined Dundee's Highlanders about 16 July, as the clans were gathering to meet the Williamite forces under Lieutenant-General Hugh Mackay. On 27 July the opposing forces met at Killiecrankie, between Aldclune and Aldgirnaig. On his extreme right flank, facing Balfour's Regiment, Dundee placed Clan Maclean, under Sir John Maclean of Duart, and Purcell's Dragoon Regiment. To their left he placed the Clanranalds, Macdonalds and Glengarrys. On the extreme left flank were the Macdonals of Sleat, and a mixed regiment under Sir Alexander Maclean. To the left center were the Camerons, under Lochiel, opposing Mackay's Regiment. The center, opposite Leven's Regiment, was left open. The Viscount Dundee commanded on the left of center with his cavalry under Sir William Wallace. Dundee held his fire until a half-hour before sunset, at which time the Highlanders charged down from the heights of Killiecrankie whooping war cries, and finally at muzzle-point, drawing their claymores and stampeding the Williamite troops. Purcell's Dragoon Regiment participated in the charge with gallantry. Iain Lom MacDonald, one of the Highlanders present, well expressed the outcome when he later wrote: -In the tender birch copse, Near the farm of MacGeorge, Full many a gay cloak lies torn. Unfortunately for the Jacobite cause the "Bonnie Dundee" was mortally wounded in the battle, and the initial advantage melted away. Purcell's Dragoon Regiment returned to Ireland and joined the squadron which had stayed behind and served with Major-General Buchan before Enniskillen on 30 July. Earlier in the summer French Marshal Conrad von Rosen had rendezvoused at Trim, while on his way to attack Enniskillen. He had written to King James II from the rendezvous on 6 June 1689 to complain that Purcell's Dragoon Regiment was not well enough equipped to fight effectively. On 29 June von Rosen noted that the Duke of Berwick was using Purcell's dragoons to fortify positions on the River Finn and later in the defence of Omagh. The regiment received a commendation by the Duke of Berwick in action near Enniskillen, in a dispatch to Lieutenant-General Richard Hamilton. On 29 August 1689 M. d'Escot wrote to Comte d'Avaux from Drogheda that Gormeston's Regiment had arrived that afternoon, and Purcell's Dragoon Regiment had arrived that evening, and listed Purcell's Regiment as composed of 12 troops for a total of 360 men, as recently determined by a review of troops. The regiment may have arrived from Bangor Bay with Brigadier Thomas Maxwell and a force of 500 horse and dragoons. The planned attack of Dundalk did not materialise, and on 6 October King James' Army fell back on Ardee, which had been converted into a defended frontier position. From Ardee, on 21 October, Comte d'Avaux wrote the French King's Minister of War, Marquis Louvois, that he had been occupied reviewing two or three petty disputes between French and Irish officers, and hoped he had finally put them to rest. The most serious dispute was between a French lieutenant and one of the dragoons from Purcell's Regiment. The French lieutenant had been seriously wounded by the dragoon in the course of an argument, and he could have been arraigned for a military court martial because Purcell had stated he had never seen the lieutenant's commission, although the lieutenant had said he had participated in all the regiment's tests of arms; had served with the regiment as an officer before Derry and Enniskillen, and had habitually bivouacked in the field with the other officers. The upshot was King James reprimanded the Irish officers who had recommended a court martial, and Comte d'Avaux acknowledging the French lieutenant was inclined to swagger and had a quick temper, sent him to his own quarters where he could care for him and dress his wounds. Another French lieutenant had served with the regiment at an earlier period, and figured in an episode in 1687. While the regiment was stationed at Cashel, Lieutenant Rene Mezandiere ordered the Deputy Mayor, Charles Robinson, cast into the common prison "a noysome place on Sunday morning." All this occurred on 25 September 1687. The Corporation petioned the Government "that ye ad Lieut. be effectually prosecuted for ye same." Later, on 27 October 1687, the Corporation records, "The chapter doe wait upon Captain Purcell to acquaint him with the injuries done by the Souldiers to the Cathedral gates, Church yard, and to them that are employed to look after them from harme or trespasses." One wonders how Colonel Nicholas dealt with this matter. During the war years, Colonel Purcell's wife and children evidently lived in France. The will of Lieutenant Pierce Power of Thurles, dated 26 June 1689, not only lists the amounts of money owed him by Colonel Purcell, but also mentions the fact his daughter, Cecily, was living with Mary Purcell of Loughmoe. The following Roster of Officers of the Regiment is taken from various French Muster Rolls of Reviews held in Ireland after the arrival of King James II. The regiment was raised mostly in Tipperary: Col. Nicholas Purcell, Commanding Officer, Lt. Col. Robert Purcell, Executive, Major Charles McDonnel, Rev. Delany, Chaplain. Troop 1. Colonel Nicholas Purcell, Lieut. James Fitzgerald, Cornet James Butler of Boytonrath (brother Sir Toby Butler, Solicitor-General), Quartermaster William Barron, and 40 dragoons. Troop 2. Lt. Col. Robert Purcell, Liut. Thomas Purcell, Coronet Anthony Purcell, Quartermaster Daniel Quinn, and 45 dragoons. Troop 3. Capt. Sir John Everard of Fethard (Cousin of Col. Purcell and brother-in-law of Capt. James Butler), Lieut. Michael Kerny, Cornet Thomas Travers, Quartermaster James Tumy, and 31 dragoons. Troop 4. Capt. Miles Bourk, Lieut. Cornelius Meagher, Cornet Bryan Meagher, Quartermaster John Fitzgerald, and 31 dragoons. Troop 5. Capt. Daniel McCarthy, Liet. Pierce Power of Thurles, Cornet Owen McCarthy, Quartermaster Edmund Meagher, and 36 dragoons. Troop 6. Capt. Anthony Morres, Lieut. John Kennedy, Cornet Hugh Kennedy, Quartermaster Richard Keating and 25 dragoons. Troop 7. Capt. John Purcell of Coneby, Kilkenny, Lieut. Theobald Purcell of Moyarde (member of the Peace Party), Cornet Hugh Purcell, Quartermaster James Wale, and 21 dragoons. Troop 8. Capt. James Butler of Grangebeg (later, 6th Baron Dunboyne), Lieut. Theobald Butler of Culecullenduff (Capt.John Purcell named executor of his will 14 December 1698), Cornet Thomas Meagh, and 31 dragoons. Troop 9. Capt. Condon, Lieut. Fitzgerald, Cornet Maly and 36 dragoons. Troop 10. Capt. Cantwell, Lieut. Condon, Cornet Hurly, and 36 dragoons. Troop 11. Capt. Edward Morres, Lieut. Ryan, Cornet Keating, and 44 dragoons. Troop 12. Capt. Tobin, Lieut. Butler, Cornet Meyrick, and 44 dragoons. The Regiment probably averaged 420 dragoons and 45 officers. During the winter of 1689 the regiment was engaged in skirmishes on the frontier, mostly around Belturbet. Battle of the Boyne The first big battle of 1690 was the Battle of the Boyne, on 1 July. King James held Colonel Browne's Infantry and Colonel Purcell's Dragoons in reserve at the Battle of the Boyne, and late in the day he committed his reserve behind the Comte de Lauzun, as the latter was about to charge the Williamite right flank which faced him within cannon shot. King James ordered Sir James Carny, the reserve commander, to move the reserve up to Lauzun's right flank and Purcell's Dragoons to dismount and engage as infantry. At this moment an aid rode up with the news that the Irish right flank had been defeated. General Sarsfield and General Maxwell rode up to say it was impossible for the horse to charge the enemy because directly ahead lay two double ditches with high banks and a brook running between them. Also at this point of time, the Williamite dragoons mounted and the whole line marched by the flank to their right in the direction of the Dublin Road. Lauzun advised the King to take his own regiment of a horse and a squadron of Purcell's Dragoons and make his way to Dublin. Sarsfield then rallied the cavalry and dragoons and covered the retreat to Dublin. The Irish Army paused at Dublin just long enough to regroup, then moved on for the defence of Limerick. King James departed Kinsale for France 2 July 1690. Limerick Purcell's Dragoon Regiment rode down to County Clare to rendezvous with the cavalry. French Major-General Boisseleau commanded the defence of Limerick, and the Williamites commenced their attack in August, and soon occupied both Ireton's Fort and Cromwell's Fort. Shortly thereafter, on 11 August 1690, Sarsfield crossed the Shannon near Killaloe with the pick of the Irish cavalry and dragoons including Purcell's Regiment. Sarsfield led his troopers through the Tipperary mountains to Ballyneety where the Williamite siege train had encamped for the night, about south-east of Limerick. They took the enemy completely by surprise, and blew up two of their guns, and destroyed 12,000 pounds of powder, match and grenades. This raid became one of Sarsfield's most celebrated exploits. Six guns salvaged from Ballyneety arrived on 16 August and the Williamite forces prepared for the forthcoming assault on Limerick. The heavy guns arrived from Waterford and the bombardment of the walls of Limerick commenced. Many fires were started by the incendiary bombs, and finally a breach was made in the wall about forty-two yards wide. General Boisseleau dug a retrenchment behind the breach, on which he mounted guns for defence. On Wednesday, 20 August 1690, an attack in force was made upon the redoubt, after two days of bombardment. The first attack was repulsed. The second attack succeeded. General Boisseleau ordered 300 of Colonel Purcell's Dragoons and 150 of Colonel Luttrell's Cavalry to make a sally from St. John's Gate and attempt to retake the redoubt. When the Irish thundered out they were savagely met by the Williamites. The besiegers lost over 300 men repulsing the sally. The Irish lost 100 men and two officers; Lt. Col. Robert Purcell and Lieutenant Pierce Power. Later, Brigadier Talbot led the Irish dragoons on a well timed sally from the spur at St. John's Gate. They were met by two enemy regiments, and after bloody encounter, forced their way through, re-entering the town through the breach and taking the besiegers from the rear. The Williamites were thrown into confusion and Boisseleau seized the moment to throw in his whole force. The Irish drove the besiegers back through the breach, over the counterscarp, back to their trenches, then back to their camp, for a complete victory after a battle of four hours. The siege of Limerick was raised and the Williamites withdrew. Deputation to St. Germain Colonel Purcell was one of those included in the deputation to St. Germain to persuade James to remove the Duke of Tyrconnell as head of the Army. The deputation was made up of Brigadier Henry Luttrell, Colonel Simon Luttrell, and Peter Creagh, Bishop of Cork. General Thomas Maxwell sailed to represent Tyrconnell. James met with the delegates, then took them to interview Louis XIV. The delegates asked for a French general to command the Irish Army. On 9 May 1691, a French convoy reached Limerick with General Charles St. Ruth, two lieutenant-generals, d'Usson and de Tessé, and Brigadier Luttrell and Colonel Purcell, and also a considerable quantity of arms, ammunition and supplies. There was confusion over who was now in charge of the army. St Ruth claimed command while Tyrconnell still claimed viceroy authority and ultimate control of the army. According to an account in the Life of James, Tyrconnell eventually submitted and left the management of the army to St. Ruth, who was superficially on good terms with him but at bottom was prejudiced against him, influenced by Luttrell and Purcell. General St. Ruth reviewed the Irish regiments on the 18th and 19 May. On 2 June John Stevens noted, "Purcell's Regiment of Horse marched out of Limerick toward the camp". With a force of , 3000 horse, and 2,000 dragoons St. Ruth had his first encounter with the Williamite forces of 18,000, commanded by Baron de Ginkel, on 21 June 1691, at Athlone. This proved to be a Jacobite defeat. St. Ruth fell back to Ballinasloe, then decided to give battle on the high ground near Aughrim, about five miles (8 km) southwest of Ballinasloe. St. Ruth took up his position on the eastern slopes of Kilcommodon Hill on 8 July. It was a good position, protected by a belt of bog along the whole front, behind which he placed his infantry. His right flank was anchored at Tristaum bridge at Urraghry Pass, and guarded by cavalry regiments of the Duke of Tyrconnell, Earl of Abercorn, and Colonel Edward Prendergast. His left flank was secured by Colonel Walter Bourk and in position in the Aughrim Castle ruin, and also guarded by the cavalry regiments of the Earl of Lucan, Brigadier Henry Luttrell and Colonel John Parker, and Colonel Purcell's Dragoon Regiment near the castle, all under the command of Major-General Dominick Sheldon. His command was subsequently weakened during the course of battle through transfer of elements of his cavalry and dragoons to the right flank. Purcell's dragoons evidently fought piecemeal, some trooper on the left flank and some on the right flank, mounted or dismounted, depending on the situation. Major Sir John Everard was killed in this action. At the beginning of the battle, elements of Sheldon's cavalry repulsed four battalions of Williamite infantry working south of the causeway. Later the Marquis de Ruvigny, leading about 14 squadrons of Williamite horse, rode up the causeway, two by two, into the fire of Irish Infantry and Purcell's dragoons in trenches, and Bourk's infantrymen in the castle ruin; passed within thirty yards of the castle; forded the stream and forced the pass, and thus enfiladed the Irish left flank. Apparently, Sheldon's cavalry was unable to turn the enemy horse. General St. Ruth was killed in battle and the Irish Army was in complete route by 9 o'clock at night. After the Battle of Aughrim, Purcell's Dragoon Regiment participated in the defence of Limerick for the second time. With the approval of Queen Mary, General Ginkel sent a communication to Tyrconnell in late July 1691 attempting to settle the battle of Limerick. Ginkel seems to have thought Tyrconnell more likely to compromise that Sarsfield "who with Luttrell and Purcell are the drivers and certainly have pensions from France". General Ginkel's gunners started the bombardment on 8 September 1691. On the night of 15 September Ginkel's forces crossed the main stream of the Shannon above Limerick. The Irish dragoons and infantry pulled back to Limerick over the Thomond bridge. The Irish cavalry rode back to Ennis. On 22 September the Williamites moved along the Clare bank of the Shannon, and up to the Irish works at the approaches to the Thomond bridge. The Irish troops were pushed back to the bridge. A French Major ordered the drawbridge pulled up, shutting out the retreating troops. Almost everyone on the bridge was killed, including Colonel Redmond (or Redmund) Stapleton of Thurlesbegg and Major Thomas Purcell, Colonel Purcell's younger brother. Siege of Limerick Limerick, now under siege on all sides, beat a parley on 24 September, and the news was sent to the Irish Cavalry near Ennis. Several delegates arrived for a parley with General Ginkel; they included the Archbishop of Cashel, the Earl of Westmeath, the Lord Dillon, the Lord Galmoy, Major-General Sheldon and Colonel Nicholas Purcell. They dined with General Ginkel, then rode on to Limerick. On 28 September, the Irish commissioners rode out to negotiate with General Ginkel. They were: Patrick, Earl of Lucan, Piercy Viscount Galmoy, Colonel Nicholas Purcell, Colonel Nicholas Cusack, Sir Toby Butler, Colonel Garrett Dillon and Colonel John Browne. The articles to the Treaty of Limerick were agreed upon 3 October between Sir Charles Porter and Thomas Coningsby, Lords Justice of Ireland, and Lieutenant-General Ginkel for the Williamites, and Patrick Earl Lucan, Piercy Viscount Galmoy, Colonel Nicholas Purcell, Colonel Garrett Dillon, and Colonel John Browne for the Irish. They secured either the right to go overseas or, if they accepted William's regime, immunity from discriminatory laws. But civil articles to secure toleration for Roman Catholics were not ratified, thus enabling later Irish leaders to denounce the "broken treaty" of Limerick. Later years Thus ended Colonel Purcell's Dragoon Regiment's service in King James II's Irish Army. Most of them went back to their homes in Tipperary and Kilkenny, although some went to France with Baron Dunboyne. Colonel Purcell chose to remain in Ireland. He was still active in the affairs of the state as can be seen when Colonel Purcell, along with Viscount Fitzwilliams of Meryon and John Seigrave, Esq. on behalf of all Roman Catholics in Ireland, signed his name to a petition read at the Council of Parliament on 28 June 1695. The petition claimed that some Bills sent from England were "injurious to the petitioners' rights" and asked for time to examine the Bills and if necessary lodge "exceptions". The petition, "after full debate, [was] rejected." On 31 October 1695 Colonel Purcell, along with Colonel Luttrell, attended the Privy Council to petition for an Act of Parliament to confirm the Articles of the Treaty of Limerick. History tells us that they were not successful. We again in the life of Colonel Purcell reach a period were only sporadic incidents are known. For an unknown reason, on 28 April 1697 the Duke of Shrewsbury wrote to the Lords of the Treasury that amongst other payments, "Col. Nicholas Purcell should have 100l." On 16 June 1699 Colonel Purcell was managing, with a Mr. Roberts, South and Savage, the estate of Viscount Kenmare, his father-in-law. Colonel Purcell is quoted as saying that "Protestant tenants will readily take it [the estate] at 3,000£ a year". On 30 March 1705 a special order was issued that issued licenses for Roman Catholics in Ireland to carry certain arms. Colonel Purcell was among the sixty or so people listed and was allowed to carry 1 sword, 1 case of pistols and 1 gun. Of Colonel Purcell's children we know the following. As already mentioned his only son fell into a vat of boiling water and died. Of his three daughters it is only known that two of them married. Catherine, his second daughter married a member of the Gaelic nobility, Domhnall, the O'Callaghan. His third daughter, married a man surnamed White from Leixlip who apparently by 1705 was not yet eighteen. In conversation with a Paul Davys, possibly a cousin, Col. Purcell's daughter stated that she "desires not to live with her husband until he is eighteen." The Purcell-Whites were the last to live in Loughmoe and did so until approximately 1760. On 4 March 1722, Colonel Nicholas Purcell of Loughmoe, 13th Baron of Loughmoe died. He was buried in the old abbey in Loughmore. For some reason, there are two stones appearing to record his death. References The Jacobite Peerage Baronetage, Knightage and Grants of Honour by the Marquis de Ruvigny and Raineval. King James' Irish Army List, 1689, by John D'Alton Journal of the Waterford & the South East of Ireland Archeological Society, Page 199 Category:1651 births Category:1722 deaths Category:Irish soldiers in the army of James II of England Category:Irish Jacobites Category:People from County Tipperary Category:18th-century Irish people Category:Irish MPs 1689 Loughmore Category:Members of the Parliament of Ireland (pre-1801) for County Tipperary constituencies
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Researchers at Karolinska Institutet and SciLifeLab have developed a new method of analysis that maps the location of proteins in the cell. The information has been compiled in a database that is accessible to researchers around the world. The method of analysis, which has been published in the journal Molecular Cell, can also provide in-depth knowledge of disrupted cell function in cancer and other diseases. Every cell in the body is made up of thousands of different proteins that are perfectly organised for the cell, and by extension our body organs, to function optimally. Cells can be compared with miniature advanced factories, where each protein has a given function and location. Proteins on the surface of the cell are used for communication between the cell and its environment. Other proteins in the cell nucleus can copy genetic material or protect it from damage. Proteins in the mitochondria produce energy for the cell, while other proteins in the proteasomes, the cell’s waste stations, break down obsolete proteins, and so on. These processes are hugely complex. Mapped the cellular locations of proteins The researchers have mapped the cellular locations of proteins by developing their own method of analysis based on mass spectrometry. This information has been compiled in a large database and released in a new publication. The database can now be used by researchers around the world who are searching for information on proteins whose function is still unknown. "The method we have developed can also be used to study whether certain diseases, such as cancer, are caused by dislocated proteins that disturb normal cell functions. It is also possible to study how cell proteins move from one location to another when the cell’s external milieu changes," says Janne Lehtiö, professor at the Department of Oncology-Pathology at Karolinska Institutet in charge of the study. Protein movement provides important information One example of the latter is the study of how around ten proteins move when cancer cells are treated with specific drugs. This provides important information about which proteins are involved in the cell's response to treatment, and thus knowledge of the drugs’ mechanisms of action. "The method also allows the published database to be expanded by other researchers worldwide, with the aim of mapping the cell’s architecture and protein functions in more detail," says Lukas Orre, researcher at the Department of Oncology-Pathology at Karolinska Institutet and principal author of the study. Complements the Human Protein Atlas The study, in combination with another Stockholm, Sweden, based project, the Human Protein Atlas, that has systematically mapped the human proteome (network of proteins), provides a greater understanding of the cell and a comprehensive map of cell proteins. Database: subcellbarcode.org The study was funded by the Swedish Foundation for Strategic Research, the Swedish Cancer Society, the Swedish Research Council, the Swedish Childhood Cancer Fund, AstraZeneca, the Cancer Research Funds of Radiumhemmet and the Stockholm County Council. Publication ”SubCellBarCode: Proteome-wide mapping of protein localization and relocalization” Lukas Minus Orre, Mattias Vesterlund, Yanbo Pan, Taner Arslan, Yafeng Zhu, Alejandro Fernandez Woodbridge, Oliver Frings, Erik Fredlund and Janne Lehtiö. Molecular Cell online 3 January, 2019.
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1. Field of the Invention The invention disclosed herein pertains generally to improvements in combustors or burners and more particularly relates to gas and liquid heaters and steam generators having an improved combustor. 2. Description of the Prior Art A vast number of burner arrangements are known for a virtually limitless number of specific uses. Typically, combustion takes place in an open combustion zone with the combustion gases then passed through a heat exchanger to heat a fluid such as air or water. Conventional combustion devices are unsatisfactory since oftentimes combustion is incomplete producing various pollutants and furthermore because the efficiency obtainable from such combustion devices is relatively poor. The known burners or combustors used for heating liquids such as water are generally quite massive and consume large amounts of fuel (usually oil or gas). Most presently used burners rely on a continuous flow of the fuel, thus perhaps wasting some of the fuel due to incomplete combustion. Combustion devices having an intermittent flow of fuel are known, for example, as in a conventional piston engine or in a pulsing combustor. Perhaps one of the first pulsing combustors was the pulse-jet engine utilized in the German V-1 rocket or buzz bomb which is described on pages 2 and 3 of the book Rocket Propulsion Elements by George P. Sutton (John Wiley & Sons, 1949.). Another known pulsing combustor is disclosed in U.S. Pat. No. 2,857,332 to Tenney et al and is utilized in a machine for producing dispersions of liquid in air or other gases. In the Tenney et al device, a fuel-air mixture is supplied through an inlet portion of a combustor with combustion air passing sequentially through a throat of an air inlet passage and over a sloping step in a fuel injection tube. Fuel is discharged as a spray and is metered in proportion to the incoming air. The fuel-air mixture is forced through a plurality of diverging passages into a combustion zone of the combustor. The passages each have a port at the combustion chamber end of each passage. Each port is covered by a finger-like portion of a metal valve preferably made of a flexible steel. The finger-like portions of the valve are sufficiently flexible to be deflected against a backing plate by the inrush of the air-fuel mixture when the burner is operating. Initially, the starting air-fuel mixture is introduced into the burner chamber and is ignited by a spark plug. The resulting explosion causes the finger-like portions of the valve to close against the intake ports leaving an exhaust tube as the only path of exit for the combustion zone gases. The mass of gases in the exhaust tube is then driven forceably at extremely high velocity outwardly of an open end of the exhaust tube by the expanding combustion gases produced by the explosion in the combustion zone. The rush of gases out of the exhaust tube causes a low pressure area in the combustion zone. The low pressure area induces a fresh charge of combustible air-fuel mixture through the ports and into the combustion zone. Fuel is fed to the combustion zone through a plurality of fuel ports and the air used is atmospheric air. The burner depends on the low pressure zone existing in the combustion chamber after exhaustion of the hot combustion products to induce a further flow of the air-fuel mixture into the combustion zone. A resonant intermittent combustion heater system using a pulsing combustion arrangement similar to the pulsing combustor disclosed in U.S. Pat. No. 2,857,332 is also known in the prior art and is disclosed in U.S. Pat. No. 2,715,390, issued to Tenney et al. A different pulsing combustion arrangement having a burner is disclosed in U.S. Pat. No. 2,959,214 issued to Durr et al. During ignition of the burner in the Durr et al device, a spark plug is activated along with a pump to supply air through a conduit under pressure to a tightly closed fuel tank. The air streaming through the tube vaporizes an amount of fuel at a diaphragm and this mixture flows into a mixing tube. The mixing tube mixes the fuel-air mixture with a further supply of air and the resulting mixture then is ignited by the spark. The burning does not provide a complete combustion of the fuel-air mixture and therefore unburned combustible components circulate within a cyclone-form combustion tube before reaching an exhaust tube. As the burner continues to operate, a part of the cyclone-form combustion tube becomes hot and the unburned combustible components which enter the cyclone combustion tube are ignited. An explosion takes place within the combustion tube and the explosion provides a sudden blast of exhaust gases through the exhaust tube. These explosions follow each other uniformly and a resonant intermittent combustion takes place providing an automatic suction of fuel and air. A spraying device having a different pulsing combustor with an oscillating burner resonator fed by a carburetor is disclosed in U.S. Pat. No. 3,758,036 issued to Bauder et al. A blower is set into operation so that a fuel whirling chamber is pressurized via a starting air pipe and fuel is supplied to the fuel whirling chamber by a tank through a nozzle. The fuel-air mixture is then supplied through a tube to the burner and an ignition device in the burner ignites the fuel-air mixture. During subsequent operation, air is drawn into a valve chamber through a suction valve provided on a front side of the carburetor and is mixed with fuel from the fuel nozzle. On a side wall of the carburetor is a lid which carries an adjusting device for the oscillating burner resonator. The adjusting device includes an air evacuating valve associated with the fuel whirling chamber and a pressure space enclosed by the lid. A diaphragm is sealed at its edges to an outside of the lid with a middle area of the diaphragm being connected to a valve closing part of the air evacuating valve. The Bauder et al patent also discloses a portable spraying apparatus having a hand held gun. The burner in the Bauder et al patent is cooled by air in a surrounding cooling cover which obtains the air from a blower through a pipe. An oscillating tube, also surrounded by the cooling cover, conducts the hot combustion products away from the burner toward a front section of the cooling cover. A liquid agent is introduced by the nozzle into the oscillating pipe so that the hot combustion products of the burner will turn the liquid into a steam or mist which will be expelled through a widened end section of the gun. A known recirculating burner is disclosed in U.S. Pat. No. 3,366,154 issued to Walsh et al which shows a compact portable burner useful in flame cultivation of crops. Some of the products of combustion are recirculated from a discharge end of the burner to a position between the discharge end and a venturi throat and just forward of an oil nozzle for the purpose of providing a clean flame and more efficient burning of the fuel. A recirculation jacket surrounds a central portion of the burner and has a top wall, a bottom wall and a pair of similar symmetrically disposed side walls in a predetermined outwardly spaced relation to top, bottom and side walls of the burner. The front ends of the jacket wall and the burner wall are joined together by a front shoulder. Similarly, the rear end of the jacket wall and the burner wall are joined together by a rear shoulder. A plurality of openings is provided in the burner walls adjacent and slightly rearwardly of the front shoulder and a similar plurality of openings is provided adjacent and slightly forwardly of the rear shoulder. Hot combustion gas enters the plurality of front shoulder openings and is recirculated to the rear and reenters the burner by venturi action at the rear shoulder openings to provide a more efficient burning of the fuel as well as improved vaporization of the fuel which is preferably fuel oil. U.S. Pat. No. 3,718,805 issued to Posey dicloses a heated fluid gun in which the fluid is heated by an electrical cartridge surrounded by a fluid channel. A fluid enters the fluid channel through a rear entrance and flows around and is heated by the heater cartridge. The heated fluid flows into a fluid expansion chamber located within a barrel of the gun. A fluid additive nozzle introduces an additional fluid such as a detergent into the stream of heated fluid downstream from the fluid expansion chamber and the heated fluid with the detergent is then discharged through an orifice located at a front surface of the gun. Another portable steam cleaner having an electrical element heating the water is disclosed in U.S. Pat. No. 2,639,365 issued to Krampe et al on May 19, 1953. Other patents and publications which disclose combustor arrangements of interest to the present invention include: U.S. Pat. No. 2,634,804 of Erickson; U.S. Pat. No. 2,589,566 of Neth et al; U.S. Pat. No. 2,077,323 of Hendrix; U.S. Pat. No. 2,411,675 of Alexander; U.S. Pat. No. 1,719,015 of Lewis; U.S. Pat. No. 1,885,040 of Arnold; U.S. Pat. No. 4,259,928 of Huber; British Pat. No. 166,455; French Pat. No. 1,366,565; and, "Pulsating Combustion: An Old Idea May Give Tomorrow's Boiler's a New Look", Power, pp. 88-91, August 1954. Accordingly, the need exists for an improved burner which provides an efficient and economical use of fuel. Such an improved burner would have particular utility in steam generation devices and in home heating equipment especially where a fluid is to be heated by the combustion.
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Maple seeds. Most people admire them for being pretty and delicate and for twirling like ballerinas when they float to the ground in fall. But this graceful dance obscures a simple fact: they are efficient flying machines. This week, Lockheed Martin is debuting an unmanned military drone that could be useful for information-gathering based on these silent, strong, one-winged, helicopter-like flyers. A foot long, the SAMARAI (after samara, the name for maple seeds) also has one wing and flies with a cyclic lift motion like a helicopter. It has two moving parts and a camera and can be controlled remotely or with an app on a tablet computer. It will be one of many new unmanned vehicles on display this week at the convention of the Association for Unmanned Vehicle Systems International in Washington, D.C. How samara fly In a manner similar to insects, hummingbirds and bats, maple seeds fly by creating a vortex over the leading edge of the wing. Reducing the pressure above the wing's surface like this creates a mini sideways tornado and the low pressure pulls the wing up, giving it twice the lift it would normally have. Because of this action, when maple seeds swirl to the ground, they go much more slowly and land farther from the tree than they otherwise would. Future applications Both the military and police could use SAMARAI. Officers could throw the drones like boomerangs to photograph what is around the next corner or inside a building and report back. Troops could also use them to get ground-level images from airplanes in addition to the aerial images typically used now. They improve upon drones currently used by the military in that they can hover in place like helicopters and take off vertically -- an advantage in tight spaces. They could one day come in different sizes and be produced cheaply with 3D printing. Watch the video below (from 2010) to see the SAMARAI be launched like a boomerang, take off vertically and land in a specific spot:
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Cosmic Loners: Orphan Stars and Planets Wander the Galaxy An artist's conception of a runaway planet zooming through interstellar space. A new paper suggests planets can blaze through space entirely by themselves, ripped free of their parent star by the power of the black hole The Milky Way contains all kinds of stars — young ones, old ones, red ones, blue ones, yellowish ones, white ones, ranging in size from much smaller than our sun to tens or even hundreds of times bigger. All told there are at least a hundred billion stars in our home galaxy — and perhaps as many as 300 billion. But a few members of this vast stellar population have a special claim to cosmic fame. They're racing away from the core of the Milky Way at speeds of up to 1.5 million m.p.h. (2.4 million km/h), on a trajectory that will ultimately take them out into intergalactic space. None of this is entirely surprising to astronomers, or at least, not any more. These so-called hypervelocity stars were predicted back in 1988; the first one was actually discovered in 2005, and by now 21 such stellar speedsters have been observed and confirmed. But a new paper slated for publication in Monthly Notices of the Royal Astronomical Society suggests that hypervelocity stars may not be the lone wolves they seem. Some of them may be taking planets along with them on their perambulations. And sometimes the planets themselves may go rogue, ripping free and fishtailing off on their own. The reason for all this galactic gadding about: the giant black hole, weighing in at more than 4 million times the mass of our sun, which lurks at the core of the Milky Way. Anything that ventures close to the core orbits the dark monster at high speed. If the "anything" happens to be a double-star system (two stars orbiting each other, which is a common thing in the Milky Way) and if the pair gets a bit too close, theory suggests that one member can fall in while the second star is flung out into deep space — kind of like the "whip" in a roller derby. (Our solar system is located a comfortable 30,000 light-years from the galactic center, so we're at no risk of being either swallowed up or hurled to oblivion.) The gravitational breakup of a pair of stellar twins explains how hypervelocity stars came to be, but when Dartmouth astrophysicist Gary Wegner, Dartmouth grad student Idan Ginsburg and his advisor, Harvard astrophysicist Avi Loeb, began looking at the phenomenon more deeply, they began to realize that not only is it entirely plausible for the stars to be accompanied by one or more planets, but also it wouldn't be all that difficult to prove the existence of such free-range solar systems. The Kepler space telescope and some Earth-based observatories have now spotted more than 2,000 so-called exoplanets orbiting distant stars. So big a head count in the brief time scientists have been searching a relatively small patch of sky suggests that there should be billions upon billions of exoplanets out there, making it entirely reasonable to conclude that at least some of them orbit hypervelocity stars. The planets themselves would be far too small and dim to see, but that's not how exoplanets are typically detected anyway. Instead, they're spotted either through the gravitational wobble they cause in their parent star or, a bit more easily, by a slight dimming in light every time the orbiting planet passes in front of the star. It's this second technique that the Kepler space probe, the ground-based MEarth Project and other observing programs use, and it doesn't even take a superpowerful instrument for them to make their discoveries, says Ginsburg. A telescope on the ground with a mirror just 13 ft. (4 m) across could do it, a relative shrimp compared with the 26- to 33-ft. (8 to 10 m) telescopes astronomers now favor. Ginsburg and his colleagues don't expect to spot any planets orbiting hypervelocity stars just yet, in part because 21 such wandering bodies are an awfully small sample group. What's more, a planet would have to be aligned just right for the light dimming to be observable. "Still," says Ginsburg, "we think it's worth looking. And if observers don't find any in this first round, they can wait for more hypervelocity stars to turn up." If such planets do exist, the odds would be exceedingly slim they'd contain life: they'd have to be in very tight orbits to avoid having been stripped away by the black hole, making things too hot for biology to get started — though planets around dim hypervelocity stars might find things a bit more comfortable. Least comfortable — and certainly loneliest — of all would be planets that were blazing through space entirely by themselves, ripped free of their parent star by the same whipcrack power of the black hole and flung free on their own. There'd be nothing, in theory at least, to prevent this from happening, and the authors of the Monthly Notices paper even went so far as to estimate just how fast the planets might be traveling: a blazing 30 million m.p.h. (48 million km/h) — or close to 5% of the speed of light — thanks mostly to their smaller mass. This is one case, of course, in which theory bumps up against the limits of technology. With no star to jostle or dim, the planets would be entirely undetectable — at least given the limits of current telescopes. It's enough, perhaps, to know that those planets may be out there, and to contemplate not just how solitary their travels are, but also how much more they'll be when they reach the end of the Milky Way and sail off into the ocean of true intergalactic space.
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entity relationship diagram erd solution Gallery Entity–relationship model An entity–relationship model (ER model for short) describes interrelated things of interest in a specific domain of knowledge. A basic ER model is composed of entity types (which classify the things of interest) and specifies relationships that can exist between entities (instances of those entity types).How to Create an Entity Relationship Diagram (ERD)An Entity Relationship Diagram (ERD) is a data model describing how entities (or concepts or things) relate to one another. When created by business analysts or business users, ERDs can be used to understand the business domain, clarify business terminology, and connect business concepts to database structures.Enhanced ER Diagram Tutorial | LucidchartEnhanced entity relationship diagrams, or EERDs, are specialized ER Diagrams that can be extremely useful for modeling your database. EERDs use several concepts that are closely related to object oriented design and programming. 3 min read Want to make an ERD of your own? Try Lucidchart. It's quickWhat is the Entity Relationship Model? Diagram & ExamplesIn this lesson, we look at a conceptual design tool commonly used in the planning and layout of a database: the entity relationship (ER) model.Database Model Diagram Symbols Edraw MaxPre drawn database model diagram symbols represent entity, view, relationship, parent to category, category, category to child, dynamic connector, line connector, strong entity, etc. These symbols help create accurate diagrams and documentation.ERD dotted line. Experts ExchangeIn an entity relationship diagram what does it mean when there is a dotted line between two entities.Draw an ER Diagram in 3 Steps edrawsoft An ER diagram is a data modeling technique showing how entities or concepts relate to one another. It's a crucial tool for software engineering during the design phase of the development process.Data Modeling an Database Design Chapter Three (unfinished)A business rule states that a given employee may be supervised—but there may be only one supervisor per employee; this means there is a mandatory recursive relationship in the ER diagram.Mechanical Drawing Symbols conceptdraw Electrical Symbols, Electrical Diagram Symbols Electrical Engineering Solution used together with ConceptDraw DIAGRAM v12 drawing facilities makes short a work of drawing various electrical and electronic circuit schemes.Data Structure Diagram | Drawing a Project Gantt Chart ...Data structure diagram (DSD) is intended for description of conceptual models of Users new to ConceptDraw PROJECT will find the Basic lessons an essential Use ConceptDraw PRO with Accounting Flowcharts solution to document and Project Accounting Diagram
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Q: Three vertices of a parallelogram have coordinates (-2,2),(1,6) and (4,3). Find all possible coordinates of the fourth vertex. Do I use the distance formula for the two points and use them to add to each other to get two parallel sides? A: If three points are $P,Q,R$ then $R+(P-Q)$ gives a fourth vertex for a parallelogram. So pick the ordered pair $(P,Q)$ in all six ways, and that gives three parallelograms. There are actually only three such paralellograms, some using my description being repeats (same vertices). So if $P,Q,R$ are the three given points (which are not collinear) the three parallelograms are those formed by using the given three vertices along with any one of the three choices $$P+Q-R,\ P+R-Q,\ Q+R-P$$ as the fourth vertex of the parallelogram. Added note: In each case the subtracted point winds up being diagonally opposite the constructed point in that parallelogram. For example, if $X=P+Q-R,$ then also $X-P=Q-R$ as expected in a parallelogram labeled going around say counterclockwise in the order $X,P,R,Q.$ The equality of the vectors $X-P$ and $Q-R$ means they are parallel and point in the same direction, so that side $XP$ is parallel to side $QR.$ And also from $X=P+Q-R$ we get $X-Q=P-R$ showing the other pair $XQ,PR$ are parallel (the remaining pair of parallel sides of that parallelogram). Suggest draw a picture to see why for this case each of $XR$ and $PQ$ wind up as "diagonals" of the parallelogram formed.
3.671875
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Diesel engine combustion is characterized by the injection of a self-ignitable fuel under very high pressure through an injector nozzle into a combustion bowl arranged in the piston. After the atomization and vaporization of the fuel in the combustion air heated to high temperatures through compression, a mixing of the already vaporized fuel components with the combustion air takes place. This carburetion is achieved on the one hand through the distribution of the fuel by means of 6- to 8-hole injector nozzles, and on the other hand through swirling air generated in the inlet channels. The chemical processing of the fuel-air mixture then occurs through cracking of the relatively long fuel molecules and the formation of active radicals. If the concentration of active radicals is sufficiently high, the self-ignition of the fuel-air mixture begins in the form of a chain reaction. The time required for the physical and chemical carburetion processes is referred to as the ignition delay. Due to the short amount of time available for carburetion as a result of the direct injection of the fuel, the remaining combustion takes place in a fuel-air mixture with locally non-homogenous fuel distribution. The ignition phase of this “non-homogenous” fuel-air mixture is characterized by the occurrence of “ignition cores” in already ignitable regions of the mixture. As combustion continues, the fuel droplets react first that have reached the compressed hot combustion air at the beginning of the injection of fuel and for which a relatively long time is thus available for mixture processing. Due to the resulting relatively faster combustion reactions, this combustion phase, which is also referred to as the combustion of “pre-mixed” mixture, is characterized by higher combustion temperatures and thus greater thermal nitrogen oxide formation and less soot formation. However, during this first combustion phase, only a certain portion of the fuel-air mixture determined by the length of the ignition delay is combusted. The remaining mixture quantity that is not yet ignitable at the moment of the start of combustion and depends on the required engine load, is first processed as the combustion process continues through steeply rising gas temperatures and an intensive charge motion and then combusts in part under lack of air at a relatively low rate of combustion. This combustion phase, which is also called “diffusion-controlled” combustion, is characterized by initial soot formation occurring as a result of local air deficiency and subsequent incomplete post-oxidation of soot with simultaneously reduced nitrogen oxide formation. The various phases of the combustion process and the corresponding mechanisms of pollutant formation yield a relationship between the nitrogen oxide and soot emissions that is typical of diesel engine combustion and is also referred to as NOx particle trade-off. This NOx particle interrelation means that, if the engine operation parameters (e.g., the injection timing) are adjusted for low NOx emissions, a simultaneous rise in soot/particle emissions is unavoidable. In order to comply with the legally prescribed pollutant emissions of diesel engines, measures are taken both within the engine and externally in the form of exhaust gas treatment processes. The most important of the measures taken within the engine to improve the fuel-air mixture formation consists in the use of high-pressure injection systems, which enable injection pressures of greater than 200 MPa. The improved breakdown of the injection spray into smaller fuel droplets achieved in this way leads to improved mixing of the fuel with the combustion air and thus to fewer rich mixture zones and, accordingly, to substantially lower soot and particle emissions. Due to the higher combustion temperatures, the carburetion intensified in this way results in higher NOx emissions, which are to be avoided through increased excess air by means of increased charge pressures and optimized injection quantity curves. Another measure is exhaust gas recirculation (EGR), which is increasingly also being used in heavy commercial vehicle engines. However, the exhaust gas return rate and thus also the possible NOx reduction through decreasing oxygen content in the combustion air are limited once again by rising soot and particle emissions. Since the described measures taken within the engine to reduce pollutants are insufficient for bringing emissions to below the exhaust gas limits, DeNOX catalytic converser systems with urea as a reduction agent and, separately from diesel engines, particle filter systems that are known for use in passenger vehicles are being used in newly approved commercial vehicle engines that must meet the requirements of Euro 5 and Euro 6 pollutant categories. To achieve the emissions goals, the raw emission behavior of the diesel engine must be adapted to the exhaust gas treatment systems used. For instance, in typical Euro 5 diesel engines, the particle emissions are reduced to the corresponding limits through flexibly tunable Common Rail (CR) injection systems with 160 to 180 MPa injection pressure, whereas the nitrogen oxide emissions are usually reduced sufficiently through the use of a urea-based DeNOx system. Sometimes, the NOx emissions are also reduced through a combination of exhaust gas recirculation and downstream DeNOx system. Which economically tenable combination of methods is used depends essentially on the raw emissions of a diesel engine. In diesel engines of the Euro 6 emissions level, the use of additional optimized injection systems with injection pressures from 200 MPa and up are required in order to further reduce particle emissions, as well as more efficient EGR-DeNOx system combinations. In particular, the use of EGR systems with substantially higher EGR rates and of DeNOx systems with NOx conversion rates of up to 90 percent is necessary. If the NOx emission limits cannot be complied with through the described use of EGR and DENOx systems, the additional use of a particle filter system with commensurately adapted tuning of the EGR and DeNOx system is unavoidable. It must therefore be noted that the Euro 5 and especially Euro 6 emissions levels applicable to heavy commercial vehicle engines can only be achieved with considerable additional technical and economic expenditure. Due to catalytic converter-related increased exhaust gas back pressure and the adaptations of the combustion process that may be required, a degradation of the fuel consumption performance can be expected for all combinations of methods for reducing NOx and particle emissions. What is being sought here in principle, however, are NOx particle emissions from the engine that are as low as possible, since that reduces the effort required on the part of exhaust gas treatment. Besides measures taken on the interior of the engine and the use of exhaust gas treatment systems, composition-modified fuels also represent an attractive possibility, in principle, for reducing harmful emissions in diesel engines. Special interest has long existed in the addition of water and other components, such as alcohol, to diesel fuel, since the nitrogen oxide-soot trade-off can be favorably influenced in this way, cf. Bach, F., Luft, M., Bartosch, S., Spicher, U.: Einfluss von Diesel-Ethanol-Wasser-Emulsionskraftstoffen auf die Dieselmotor-Emmissionen [Influence of diesel-ethanol-water emulsion fuels on diesel engine emissions]. MTZ 05/2011, pp. 408-414. When using water-in-diesel fuel emulsion, either a ready-to-use water-diesel emulsion is injected into the combustion chamber instead of pure diesel fuel while using an emulsifying additive or an emulsion produced on board the vehicle by the existing injection system. The production of the emulsion in the vehicle has the advantage that the water fraction in the mixed fuel can be selected relatively freely in consideration of the technical limits of combustion with regard to the maximum reduction of pollutants. In principle, besides the use of water-in-diesel fuel emulsions, it is also possible to exploit the advantageous characteristics of water to reduce combustion temperatures through the injection of water into the intake air and the direct injection of the water into the combustion chamber. Due to the high enthalpy of vaporization of the water, when it is added through the intake pipe and especially when it is injected directly, substantial cooling of the intake air or combustion air is achieved in the cylinder and thus also a reduction in nitrogen oxide emissions of up to 50 percent. Due to the relatively little mixing of the diesel fuel with water in the combustion chamber and the resulting lesser homogenization of the diesel fuel in the combustion chamber in comparison to emulsion fuels, however, the reduction of the soot emissions ends up being less; cf. DE 10 2009 048 223 A1. Emulsion fuels therefore offer, in addition to easier use in series engines, greater potential for reducing the critical harmful components in the exhaust gas of diesel engines. Water-diesel emulsions can be regarded as disperse multi-phase systems of at least two liquids insoluble in a mixture in which water is regarded as the inner, disperse phase. Accordingly, diesel fuel represents the outer phase, the dispersant. Water-diesel emulsions are not thermodynamically stable and separate after a relatively short standing time. Through the use of emulsifying additives, so-called emulsifiers, it is possible, in principle, to convert a water-diesel emulsion into a thermodynamically stable form. One criterion that is important for the suitability of an emulsion as fuel for diesel engines is that the water droplets be distributed as finely as possible in the diesel fuel. Emulsions produced in the vehicle using an emulsifier or, if no emulsifier is used, using an appropriate mixing device are suitable for mobile use. Emulsions produced outside of the vehicle, such as those available at gas stations, for example, have a constant composition that is not adapted to the requirements of the engine operation and therefore does not achieve full potential in terms of the reduction of emissions and consumption. The effect of water-diesel emulsions consists, on the one hand, in a temperature reduction occurring during the water vaporization and, on the other hand, in reduced combustion temperatures as a result of the increased inert gas fraction in the form of water vapor. Both lead to a lengthening of the physical ignition delay, which leads to a more uniform (homogeneous) distribution of the fuel in the combustion chamber and thus to a greater proportion of “pre-mixed” combustion. The resulting intensified homogenization of the mixture in conjunction with the water droplets being finely distributed in the emulsion leads to a reduction of highly fuel-rich regions of the mixture, which are substantially responsible for the occurrence of soot during the combustion process. The reduction of the nitrogen oxide emissions can be attributed to a significant flame temperature reduction both as a result of the high enthalpy of vaporization of the water and the water-related lower local specific heat release in the combustion zone; cf. Pittermann, R., Hinz, M., Kauert, L: Einfluss von Abgasrückführung und Kraftstoff-Wasser-Emulsion auf Verbrennungsablauf und Schadstoffbildung im Dieselmotor [Influence of exhaust gas recirculation and fuel-water emulsion on combustion process and pollutant formation in the diesel engine]. MTZ 60(1999)12, pp. 812-818. The frequently used exhaust gas recirculation (EGR) for reducing the NOx emissions also brings about lower flame temperatures in accordance with the increased inert gas fraction. However, increased soot emissions occur at higher EGR rates, which can be avoided in the combination with water-diesel emulsion fuels. The use of water-diesel emulsion fuels thus increases EGR tolerance and hence the potential for reducing NOx and soot. Another requirement for the optimal use of an emulsion fuel is the need to adapt the water fraction in the emulsion to different engine operating states, and to engine shutdown and startup even after extended non-operation. In the starting phase of the diesel engine, reliable and quick startup and quick heating of the engine can only be achieved in pure diesel fuel operation, since stable combustion is already achieved after several stroke cycles. When using a water-diesel emulsion in the starting phase as well, the number of stroke cycles without combustion increases as a result of the worsened self-ignitability of the emulsion, with commensurately increased emissions of uncombusted fuel. As the engine warms up, the water fraction in the emulsion can be increased in the warm-up phase. In the case of predominantly stationary engine operation and high output, a greater proportion of water can be contained in the emulsion due to the higher combustion chamber temperatures in order to thus achieve a combustion process that is as efficient as possible along with simultaneously high reduction of NOx and particle emissions. In low load states and commensurately low combustion chamber temperatures, a reduction of the water fraction in the emulsion is necessary in order to prevent excessive cooling of the flame zones and the associated emissions of uncombusted fuel. Predominantly stationary engine operation with only relatively slow changes in load and engine speed does not require dynamic emulsifying systems. In principle, the use of the full potential of a water-diesel emulsion in terms of reduced NOx and soot is only possible if the water fraction is as close as possible to the respective technical combustion limit, as a function of the operating point. For the dynamic operation that usually occurs with automobiles, this means that it is absolutely necessary to have a very quick adaptation of the water fraction to the momentary combustion chamber temperatures and to the oxygen content available for combustion while making use of exhaust gas recirculation. The quicker the adaptation of the water fraction to the momentary operating state of the engine, the greater the reduction in emissions. This is all the more important given that the determination of the emissions behavior of diesel engines is done for commercial vehicles and mobile working machines using transient exhaust gas test cycles.
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Judaism: The Oral Law -Talmud & Mishna The Oral Law is a legal commentary on the Torah, explaining how its commandments are to be carried out. Common sense suggests that some sort of oral tradition was always needed to accompany the Written Law, because the Torah alone, even with its 613 commandments, is an insufficient guide to Jewish life. For example, the fourth of the Ten Commandments, ordains, "Remember the Sabbath day to make it holy" (Exodus 20:8). From the Sabbath's inclusion in the Ten Commandments, it is clear that the Torah regards it as an important holiday. Yet when one looks for the specific biblical laws regulating how to observe the day, one finds only injunctions against lighting a fire, going away from one's dwelling, cutting down a tree, plowing and harvesting. Would merely refraining from these few activities fulfill the biblical command to make the Sabbath holy? Indeed, the Sabbath rituals that are most commonly associated with holiness-lighting of candles, reciting the kiddush, and the reading of the weekly Torah portion are found not in the Torah, but in the Oral Law. Without an oral tradition, some of the Torah's laws would be incomprehensible. In the Shema's first paragraph, the Bible instructs: "And these words which I command you this day shall be upon your heart. And you shall teach them diligently to your children, and you shall talk of them when you sit in your house, when you walk on the road, when you lie down and when you rise up. And you shall bind them for a sign upon your hand, and they shall be for frontlets between your eyes." "Bind them for a sign upon your hand," the last verse instructs. Bind what? The Torah doesn't say. "And they shall be for frontlets between your eyes." What are frontlets? The Hebrew word for frontlets, totafot is used three times in the Torah — always in this context (Exodus 13:16; Deuteronomy 6:8, 11:18) — and is as obscure as is the English. Only in the Oral Law do we learn that what a Jewish male should bind upon his hand and between his eyes are tefillin (phylacteries). Finally, an Oral Law was needed to mitigate certain categorical Torah laws that would have caused grave problems if carried out literally. The Written Law, for example, demands an "eye for an eye" (Exodus 21:24). Did this imply that if one person accidentally blinded another, he should be blinded in return? That seems to be the Torah's wish. But the Oral Law explains that the verse must be understood as requiring monetary compensation: the value of an eye is what must be paid. The Jewish community of Palestine suffered horrendous losses during the Great Revolt and the Bar-Kokhba rebellion. Well over a million Jews were killed in the two ill-fated uprisings, and the leading yeshivot, along with thousands of their rabbinical scholars and students, were devastated. This decline in the number of knowledgeable Jews seems to have been a decisive factor in Rabbi Judah the Prince's decision around the year 200 C.E. to record in writing the Oral Law. For centuries, Judaism's leading rabbis had resisted writing down the Oral Law. Teaching the law orally, the rabbis knew, compelled students to maintain close relationships with teachers, and they considered teachers, not books, to be the best conveyors of the Jewish tradition. But with the deaths of so many teachers in the failed revolts, Rabbi Judah apparently feared that the Oral Law would be forgotten unless it were written down. In the Mishna, the name for the sixty-three tractates in which Rabbi Judah set down the Oral Law, Jewish law is systematically codified, unlike in the Torah. For example, if a person wanted to find every law in the Torah about the Sabbath, he would have to locate scattered references in Exodus, Leviticus, and Numbers. Indeed, in order to know everything the Torah said on a given subject, one either had to read through all of it or know its contents by heart. Rabbi Judah avoided this problem by arranging the Mishna topically. All laws pertaining to the Sabbath were put into one tractate called Shabbat (Hebrew for "Sabbath"). The laws contained in Shabbat's twenty-four chapters are far more extensive than those contained in the Torah, for the Mishna summarizes the Oral Law's extensive Sabbath legislation. The tractate Shabbat is part of a larger "order" called Mo'ed (Hebrew for "holiday"), which is one of six orders that comprise the Mishna. Some of the other tractates in Mo'ed specify the Oral Laws of Passover (Pesachim); Purim (Megillah); Rosh ha­Shana; Yom Kippur (Yoma); and Sukkot. The first of the six orders is called Zera'im (Seeds), and deals with the agricultural rules of ancient Palestine, particularly with the details of the produce that were to be presented as offerings at the Temple in Jerusalem. The most famous tractate in Zera'im, however, Brakhot (Blessings) has little to do with agriculture. It records laws concerning different blessings and when they are to be recited. Another order, Nashim (Women), deals with issues between the sexes, including both laws of marriage, Kiddushin, and of divorce, Gittin. A fifth order, Kodashim, outlines the laws of sacrifices and ritual slaughter. The sixth order, Taharot, contains the laws of purity and impurity. Although parts of the Mishna read as dry legal recitations, Rabbi Judah frequently enlivened the text by presenting minority views, which it was also hoped might serve to guide scholars in later generations (Mishna Eduyot 1:6). In one famous instance, the legal code turned almost poetic, as Rabbi Judah cited the lengthy warning the rabbinic judges delivered to witnesses testifying in capital cases: "How are witnesses inspired with awe in capital cases?" the Mishna begins. "They are brought in and admonished as follows: In case you may want to offer testimony that is only conjecture or hearsay or secondhand evidence, even from a person you consider trustworthy; or in the event you do not know that we shall test you by cross-examination and inquiry, then know that capital cases are not like monetary cases. In monetary cases, a man can make monetary restitution and be forgiven, but in capital cases both the blood of the man put to death and the blood of his [potential] descendants are on the witness's head until the end of time. For thus we find in the case of Cain, who killed his brother, that it is written: 'The bloods of your brother cry unto Me' (Genesis 4:10) — that is, his blood and the blood of his potential descendants.... Therefore was the first man, Adam, created alone, to teach us that whoever destroys a single life, the Bible considers it as if he destroyed an entire world. And whoever saves a single life, the Bible considers it as if he saved an entire world. Furthermore, only one man, Adam, was created for the sake of peace among men, so that no one should say to his fellow, 'My father was greater than yours.... Also, man [was created singly] to show the greatness of the Holy One, Blessed be He, for if a man strikes many coins from one mold, they all resemble one another, but the King of Kings, the Holy One, Blessed be He, made each man in the image of Adam, and yet not one of them resembles his fellow. Therefore every single person is obligated to say, 'The world was created for my sake"' (Mishna Sanhedrin 4:5). (One commentary notes, "How grave the responsibility, therefore, of corrupting myself by giving false evidence, and thus bringing [upon myself the moral guilt of [murdering] a whole world.") One of the Mishna's sixty­three tractates contains no laws at all. It is called Pirkei Avot (usually translated as Ethics of the Fathers), and it is the "Bartlett's" of the rabbis, in which their most famous sayings and proverbs are recorded. During the centuries following Rabbi Judah's editing of the Mishna, it was studied exhaustively by generation after generation of rabbis. Eventually, some of these rabbis wrote down their discussions and commentaries on the Mishna's laws in a series of books known as the Talmud. The rabbis of Palestine edited their discussions of the Mishna about the year 400: Their work became known as the Palestinian Talmud (in Hebrew, Talmud Yerushalmi, which literally means "Jerusalem Talmud"). More than a century later, some of the leading Babylonian rabbis compiled another editing of the discussions on the Mishna. By then, these deliberations had been going on some three hundred years. The Babylon edition was far more extensive than its Palestinian counterpart, so that the Babylonian Talmud (Talmud Bavli) became the most authoritative compilation of the Oral Law. When people speak of studying "the Talmud," they almost invariably mean the Bavli rather than the Yerushalmi. The Talmud's discussions are recorded in a consistent format. A law from the Mishna is cited, which is followed by rabbinic deliberations on its meaning. The Mishna and the rabbinic discussions (known as the Gemara) comprise the Talmud, although in Jewish life the terms Gemara and Talmud usually are used interchangeably. The rabbis whose views are cited in the Mishna are known as Tanna'im (Aramaic for "teachers"), while the rabbis quoted in the Gemara are known as Amora'im ("explainers" or "interpreters"). Because the Tanna'im lived earlier than the Amora'im, and thus were in closer proximity to Moses and the revelation at Sinai, their teachings are considered more authoritative than those of the Amora'im. For the same reason, Jewish tradition generally regards the teachings of the Amora'im, insofar as they are expounding the Oral Law, as more authoritative than contemporary rabbinic teachings. In addition to extensive legal discussions (in Hebrew, halakha), the rabbis incorporated into the Talmud guidance on ethical matters, medical advice, historical information, and folklore, which together are known as aggadata. As a rule, the Gemara's text starts with a close reading of the Mishna. For example, Mishna Bava Mezia 7:1 teaches the following: "If a man hired laborers and ordered them to work early in the morning and late at night, he cannot compel them to work early and late if it is not the custom to do so in that place." On this, the Gemara (Bava Mezia 83a) comments: "Is it not obvious [that an employer cannot demand that they change from the local custom]? The case in question is where the employer gave them a higher wage than was normal. In that case, it might be argued that he could then say to them, 'The reason I gave you a higher wage than is normal is so that you will work early in the morning and late at night.' So the law tells us that the laborers can reply: 'The reason that you gave us a higher wage than is normal is for better work [not longer hours].'" Among religious Jews, talmudic scholars are regarded with the same awe and respect with which secular society regards Nobel laureates. Yet throughout Jewish history, study of the Mishna and Talmud was hardly restricted to an intellectual elite. An old book saved from the millions burned by the Nazis, and now housed at the YIVO library in New York, bears the stamp THE SOCIETY OF WOODCHOPPERS FOR THE STUDY OF MISHNA IN BERDITCHEV. That the men who chopped wood in Berditchev, an arduous job that required no literacy, met regularly to study Jewish law demonstrates the ongoing pervasiveness of study of the Oral Law in the Jewish community.
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Vehicle armour Military vehicles are commonly armoured (or armored; see spelling differences) to withstand the impact of shrapnel, bullets, missiles or shells, protecting the personnel inside from enemy fire. Such vehicles include armoured fighting vehicles like tanks, aircraft and ships. Civilian vehicles may also be armoured. These vehicles include cars used by officials (e.g., presidential limousines), reporters and others in conflict zones or where violent crime is common. Civilian armoured cars are also routinely used by security firms to carry money or valuables to reduce the risk of highway robbery or the hijacking of the cargo. Armour may also be used in vehicles to protect from threats other than a deliberate attack. Some spacecraft are equipped with specialised armour to protect them against impacts from micrometeoroids or fragments of space junk. Modern aircraft powered by jet engines usually have them fitted with a sort of armour in the form of an aramid composite kevlar bandage around the fan casing or debris containment walls built into the casing of their gas turbine engines to prevent injuries or airframe damage should the fan, compressor, or turbine blades break free. The design and purpose of the vehicle determines the amount of armour plating carried, as the plating is often very heavy and excessive amounts of armour restrict mobility. In order to decrease this problem, some new materials (nanomaterials) and material compositions are being researched which include buckypaper, and aluminium foam armour plates. Materials Metals Steel Rolled homogeneous armour is strong, hard, and tough (does not shatter when struck with a fast, hard blow). Steel with these characteristics are produced by processing cast steel billets of appropriate size and then rolling them into plates of required thickness. Rolling and forging (hammering the steel when it is red hot) irons out the grain structure in the steel, removing imperfections which would reduce the strength of the steel. Rolling also elongates the grain structure in the steel to form long lines, which enable the stress the steel is placed under when loaded to flow throughout the metal, and not be concentrated in one area. Aluminium Aluminium is used when light weight is a necessity. It is most commonly used on APCs and armoured cars. While certainly not the strongest metal, it is cheap, lightweight, and tough enough that it can serve as easy armor. Iron Wrought iron was used on ironclad warships. Early European iron armour consisted of 10 to 13 cm of wrought iron backed by up to one meter of solid wood. It has since been supplemented by Steel due to steel being significantly stronger. Titanium Titanium has almost twice the density of aluminium, but is as strong as iron. So, despite being more expensive, it finds an application in areas where weight is a concern, such as personal armour and military aviation. Some notable examples of its use include the USAF A-10 Thunderbolt II and the Soviet/Russian-built Sukhoi Su-25 ground-attack aircraft, utilising a bathtub-shaped titanium enclosure for the pilot, as well as the Soviet/Russian Mil Mi-24 attack helicopter. Uranium Because of its high density, depleted uranium can also be used in tank armour, sandwiched between sheets of steel armour plate. For instance, some late-production M1A1HA and M1A2 Abrams tanks built after 1998 have DU reinforcement as part of the armour plating in the front of the hull and the front of the turret, and there is a program to upgrade the rest (see Chobham armour). Plastic Plastic metal was a type of vehicle armour originally developed for merchant ships by the British Admiralty in 1940. The original composition was described as 50% clean granite of half-inch size, 43% of limestone mineral, and 7% of bitumen. It was typically applied in a layer two inches thick and backed by half an inch of steel. Plastic armour was highly effective at stopping armour piercing bullets because the hard granite particles would deflect the bullet, which would then lodge between plastic armour and the steel backing plate. Plastic armour could be applied by pouring it into a cavity formed by the steel backing plate and a temporary wooden form. Some main battle tank (MBT) armour utilises polymers, for example polyurethane as used in the 'BDD' applique armor applied to modernized T-62 and T-55. Glass Bulletproof glass is a colloquial term for glass that is particularly resistant to being penetrated when struck by bullets. The industry generally refers to it as bullet-resistant glass or transparent armour. Bullet-resistant glass is usually constructed using a strong but transparent material such as polycarbonate thermoplastic or by using layers of laminated glass. The desired result is a material with the appearance and light-transmitting behaviour of standard glass, which offers varying degrees of protection from small arms fire. The polycarbonate layer, usually consisting of products such as Armormax, Makroclear, Cyrolon, Lexan or Tuffak, is often sandwiched between layers of regular glass. The use of plastic in the laminate provides impact-resistance, such as physical assault with a hammer, an axe, etc. The plastic provides little in the way of bullet-resistance. The glass, which is much harder than plastic, flattens the bullet and thereby prevents penetration. This type of bullet-resistant glass is usually 70–75 mm (2.8–3.0 in) thick. Bullet-resistant glass constructed of laminated glass layers is built from glass sheets bonded together with polyvinyl butyral, polyurethane or ethylene-vinyl acetate. This type of bullet-resistant glass has been in regular use on combat vehicles since World War II; it is typically about 100–120 mm (3.9–4.7 in) thick and is usually extremely heavy. Newer materials are being developed. One such, aluminium oxynitride, is much lighter but at US$10–15 per square inch is much more costly. Ceramic Ceramic's precise mechanism for defeating HEAT was uncovered in the 1980s. High speed photography showed that the ceramic material shatters as the HEAT round penetrates, the highly energetic fragments destroying the geometry of the metal jet generated by the hollow charge, greatly diminishing the penetration. Ceramic layers can also be used as part of composite armour solutions. The high hardness of some ceramic materials serves as a disruptor that shatters and spreads the kinetic energy of projectiles. Composite Composite armour is armour consisting of layers of two or more materials with significantly different physical properties; steel and ceramics are the most common types of material in composite armour. Composite armour was initially developed in the 1940s, although it did not enter service until much later and the early examples are often ignored in the face of newer armour such as Chobham armour. Composite armour's effectiveness depends on its composition and may be effective against kinetic energy penetrators as well as shaped charge munitions; heavy metals are sometimes included specifically for protection from kinetic energy penetrators. Composite armour used on modern Western and Israeli main battle tanks largely consists of non-explosive reactive armour (NERA) elements - a type of Reactive armour. These elements are often a laminate consisting of two hard plates (usually high hardness steel) with some low density interlayer material between them. Upon impact, the interlayer swells and moves the plates, disrupting heat 'jets' and possibly degrading kinetic energy projectiles. Behind these elements will be some backing element designed to stop the degraded jet or projectile element, which may be of high hardness steel, or some composite of steel and ceramic or possibly uranium. Soviet main battle tanks from the T-64 onward utilised composite armor which often consisted of some low density filler between relatively thick steel plates or castings, for example Combination K. For example, the T-64 turret front and cheek was originally filled with aluminum, and then ceramic balls and aluminum, whilst some models of the T-72 features a glass filler called 'Kvartz'. The tank glacis was often a sandwich of steel and some low density filler, either textolite (a fibreglass reinforced polymer) or ceramic plates. Later T-80 and T-72 turrets contained NERA elements, similar to those discussed above. Ships Belt armour is a layer of armour-plating outside the hull (watercraft) of warships, typically on battleships, battlecruisers, cruisers and some aircraft carriers. Typically, the belt covered from the deck down someway below the waterline of the ship. If built within the hull, rather than forming the outer hull, it could be fitted at an inclined angle to improve the protection. When struck by a shell or torpedo, the belt armour is designed to prevent penetration, by either being too thick for the warhead to penetrate, or sloped to a degree that would deflect either projectile. Often, the main belt armour was supplemented with a torpedo bulkhead spaced several meters behind the main belt, designed to maintain the ship's watertight integrity even if the main belt were penetrated. The air-space between the belt and the hull also adds buoyancy. Several wartime vessels had belt armour that was thinner or shallower than was desirable, to speed production and conserve resources. Aircraft Armour plating is not common on aircraft, which generally rely on their speed and manoeuvrability to avoid ground fire, rather than trying to resist impacts. Additionally, any armour capable of stopping large-calibre anti-aircraft fire or missile fragments would result in an unacceptable weight penalty. So, only the vital parts of an aircraft, such as the ejection seat and engines, are usually armoured. This is one area where titanium is used extensively as armour plating. For example, in the American Fairchild Republic A-10 Thunderbolt II and the Soviet-built Sukhoi Su-25 ground attack aircraft, as well as the Mil Mi-24 Hind ground-attack helicopter, the pilot sits in a titanium enclosure known as the "bathtub" for its shape. In addition, the windscreens of larger aircraft are generally made of impact-resistant, laminated materials, even on civilian craft, to prevent damage from bird strikes or other debris. Armoured fighting vehicles The most heavily armoured vehicles today are the main battle tanks, which are the spearhead of the ground forces, and are designed to withstand anti-tank missiles, kinetic energy penetrators, NBC threats and in some tanks even steep-trajectory shells. The Israeli Merkava tanks were designed in a way that each tank component functions as additional back-up armour to protect the crew. Outer armour is modular and enables quick replacement of damaged armour. Layout For efficiency, the heaviest armour on an armoured fighting vehicle (AFV) is placed on its front. Tank tactics require the vehicle to always face the likely direction of enemy fire as much as possible, even in defence or withdrawal operations. Sloping and curving armour can both increase its protection. Given a fixed thickness of armour plate, a projectile striking at an angle must penetrate more armour than one impacting perpendicularly. An angled surface also increases the chance of deflecting a projectile. This can be seen on v-hull designs, which direct the force of an Improvised explosive device or landmine away from the crew compartment, increasing crew survivability. Spall liners Beginning during the Cold War, many AFVs have spall liners inside of the armour, designed to protect crew and equipment inside from fragmentation (spalling) released from the impact of enemy shells, especially high explosive squash head warheads. Spall liners are made of Kevlar, Dyneema, Spectra Shield, or similar materials. Appliqué Appliqué armour, or add-on armour, consists of extra plates mounted onto the hull or turret of an AFV. The plates can be made of any material and are designed to be retrofitted to an AFV to withstand weapons that can penetrate the original armour of the vehicle. An advantage of appliqué armour is the possibility to tailor the vehicle's protection level to a specific threat scenario. Improvised Vehicle armour is sometimes improvised in the midst of an armed conflict by vehicle crews or individual units. In World War II, British, Canadian and Polish tank crews welded spare strips of tank track to the hulls of their Sherman tanks. U.S. tank crews often added sand bags in the hull and turrets on Sherman tanks, often in an elaborate cage made of girders. Some Sherman tanks were up-armoured in the field with glacis plates and other armour cut from knocked-out tanks to create Improvised Jumbos, named after the heavily armoured M4A3E2 assault tank. In the Vietnam War, U.S. "gun trucks" were armoured with sandbags and locally fabricated steel armour plate. More recently, U.S. troops in Iraq armoured Humvees and various military transport vehicles with scrap materials: this came to be known as "hillbilly armor" or "haji armor" by the Americans. Moreover, there was the Killdozer incident, with the modified bulldozer being armored with steel and concrete composite, which proved to be highly resistant to small arms. Spaced Armour with two or more plates spaced a distance apart, called spaced armour, has been in use since the First World War, where it was used on the Schneider CA1 and Saint-Chamond tanks. Spaced armour can be advantageous in several situations. For example, it can reduce the effectiveness of kinetic energy penetrators because the interaction with each plate can cause the round to tumble, deflect, deform, or disintegrate. This effect can be enhanced when the armour is sloped. Spaced armour can also offer increased protection against HEAT projectiles. This occurs because the shaped charge warhead can detonate prematurely (at the first surface), so that the metal jet that is produced loses its coherence before reaching the main armour and impacting over a broader area. Sometimes the interior surfaces of these hollow cavities are sloped, presenting angles to the anticipated path of the shaped charge's jet in order to further dissipate its power. Taken to the extreme, relatively thin armour plates, metal mesh, or slatted plates, much lighter than fully protective armour, can be attached as side skirts or turret skirts to provide additional protection against such weapons. This can be seen in middle and late-World War II German tanks, as well as many modern AFVs. Taken as a whole, spaced armour can provide significantly increased protection while saving weight. The analogous Whipple shield uses the principle of spaced armour to protect spacecraft from the impacts of very fast micrometeoroids. The impact with the first wall melts or breaks up the incoming particle, causing fragments to be spread over a wider area when striking the subsequent walls. Sloped Sloped armour is armour that is mounted at a non-vertical and non-horizontal angle, typically on tanks and other armoured fighting vehicles. For a given normal to the surface of the armour, its plate thickness, increasing armour slope improves the armour's level of protection by increasing the thickness measured on a horizontal plane, while for a given area density of the armour the protection can be either increased or reduced by other sloping effects, depending on the armour materials used and the qualities of the projectile hitting it. The increased protection caused by increasing the slope while keeping the plate thickness constant, is due to a proportional increase of area density and thus mass, and thus offers no weight benefit. Therefore, the other possible effects of sloping, such as deflection, deforming and ricochet of a projectile, have been the reasons to apply sloped armour in armoured vehicles design. Another motive is the fact that sloping armour is a more efficient way of covering the necessary equipment since it encloses less volume with less material. The sharpest angles are usually seen on the frontal glacis plate, both as it is the hull side most likely to be hit and because there is more room to slope in the longitudinal direction of a vehicle. Reactive Explosive reactive armour, initially developed by German researcher Manfred Held while working in Israel, uses layers of high explosive sandwiched between steel plates. When a shaped-charge warhead hits, the explosive detonates and pushes the steel plates into the warhead, disrupting the flow of the charge's liquid metal penetrator (usually copper at around 500 degrees Celsius; it can be made to flow like water by sufficient pressure). Traditional "light" ERA is less effective against kinetic penetrators. "Heavy" reactive armour, however, offers better protection. The only example currently in widespread service is Russian Kontakt-5. Explosive reactive armour poses a threat to friendly troops near the vehicle. Non-explosive reactive armour is an advanced spaced armour which uses materials which change their geometry so as to increase protection under the stress of impact. Active protection systems use a sensor to detect an incoming projectile and explosively launch a counter-projectile into its path. Slat Slat armour is designed to protect against anti-tank rocket and missile attacks, where the warhead is a shaped charge. The slats are spaced so that the warhead is either partially deformed before detonating, or the fuzing mechanism is damaged, thereby preventing detonation entirely. As shaped charges rely on very specific structure to create a jet of hot metal, any disruption to this structure greatly reduces the effectiveness of the warhead. Slat armour can be defeated by tandem-charge designs such as the RPG-27 and RPG-29. Electrically charged Electrically charged armour is a recent development in the United Kingdom by the Defence Science and Technology Laboratory. A vehicle is fitted with two thin shells, separated by insulating material. The outer shell holds an enormous electric charge, while the inner shell is at ground. If an incoming HEAT jet penetrates the outer shell and forms a bridge between the shells, the electrical energy discharges through the jet, disrupting it. Trials have so far been extremely promising, and it is hoped that improved systems could protect against KE penetrators. The developers of the Future Rapid Effect System (FRES) series of armoured vehicles are considering this technology. See also Active protection system Armoured fighting vehicle Armoured forces Main battle tank Non-military armoured vehicles Personal armour Plastic armour References External links Electrically charged armour Defense Systems - Idaho National Laboratory - New Light Armor Modern armoured vehicles Category:Armoured warfare Category:History of the tank
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Lime sulfur In horticulture, lime sulfur (British spelling lime sulphur) is a mixture of calcium polysulfides formed by reacting calcium hydroxide with sulfur, used in pest control. It can be prepared by boiling calcium hydroxide and sulfur together with a small amount of surfactant. It is normally used as an aqueous solution, which is reddish-yellow in colour and has a distinctive offensive odour. Creating lime sulfur A New York State Agricultural Experiment Station recipe for the concentrate is 80 lb. of sulfur, 36 lb. of quicklime, and 50 gal. of water. About 2.2:1 is the ratio (by weight) for compounding sulfur and quicklime; this makes the highest proportion of calcium pentasulfide. If calcium hydroxide (builders or hydrated lime) is used, an increase by 1/3 or more (to 115 g/L or more) might be used with the 192 g/L of sulfur. If the quicklime is 85%, 90%, or 95% pure, use 101 g/L, 96 g/L, or 91 g/L; if impure hydrated lime is used, similarly increase its quantity. Avoid using lime that is less than 90% pure. Boil for an hour, stirring and adding small amounts of hot water to compensate for evaporation. Use Lime sulfur is sold as a spray for deciduous trees to control fungi, bacteria and insects living or dormant on the surface of the bark. Lime sulfur burns leaves so it is not as useful for evergreen plants. Bonsai enthusiasts use undiluted lime sulfur to bleach, sterilise, and preserve deadwood on bonsai trees while giving an aged look. Rather than spraying the entire tree, as with the pesticidal usage, lime sulfur is painted directly onto the exposed deadwood, and is often colored with a small amount of dark paint to make it look more natural. Without paint pigments, the lime-sulfur solution bleaches wood to a bone-white color that takes time to weather and become natural-looking. Because the lime sulfur does not contact the leaves or needles, this technique can be used on evergreen trees as well as other types of trees. Diluted solutions of lime sulfur (between 1:16 and 1:32) are also used as a dip for pets to help control ringworm (fungus), mange and other dermatoses and parasites. Undiluted lime sulfur is corrosive to skin and eyes and can cause serious injury like blindness. Safety Lime sulfur reacts with strong acids (including stomach acid) to produce highly toxic hydrogen sulfide (rotten egg gas) and indeed usually has a distinct "rotten egg" odor to it. Lime sulfur is not extremely flammable but combustion produces highly irritating sulfur dioxide gas. Safety goggles and gloves should be worn while handling lime sulfur. Lime sulfur solutions are strongly alkaline (typical commercial concentrates have a pH over 11.5), and so it is corrosive to living things and can cause blindness if splashed in the eyes. History Lime sulfur is believed to be the earliest synthetic chemical used as a pesticide, being used in the 1840s in France to control grape vine powdery mildew Uncinula necator, which had been introduced from the USA in 1845 and reduced wine production by 80%. In 1886 it was first used in California to control San Jose scale. Commencing around 1904, commercial suppliers began to manufacturer lime sulfur; prior to that time, gardeners were expected to manufacture their own. By the 1920s essentially all commercial orchards in western countries were protected by regular spraying with lime sulfur. However by the 1940s, lime sulfur began to be replaced by synthetic organic fungicides which risked less damage to the crop's foliage. References Notes Bibliography "Chemical Investigation of Best Conditions for Making the Lime-Sulfur Wash." L.L. Van Slyke, A.W. Bosworth, & C.C. Hedges, New York Agricultural Experiment Station Bulletin No. 329, December 1910, Geneva, New York External links Chronological History of the Development of Insecticides and Control Equipment from 1854 through 1954 Background on History of Pesticide Use and Regulation in the United States, Part Two (PDF, 54 kB). The Value of Fungicides in U.S. Crop Production, (PDF, 1.1 MB) Category:Pest control Category:Fungicides Category:Insecticides Category:Calcium compounds Category:Sulfur compounds Category:Alchemical substances
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Q: Abundant numbers list in Python Working in python I need to return a list of the first n abundant numbers in ascending order. An abundant number is an integer that is less than the sum of its perfect divisors. For example, 12 is an abundant number because its perfect divisors (1, 2, 3, 4, and 6) add up to 16. The function abundant(n) should return a list containing exactly the first n abundant numbers in ascending order. For example, abundant(7) would return a list with the first seven abundant numbers. I have tried to use: def abundant(n): def factors(value): factors = [x for x in range(1, value + 1 // 2 + 1) if value % x == 0] return factors if sum(factors) > value: return value abundant = factors() return abundant[:n] A: I'm not an expert in python, but I'd recommend a for loop, so: # From 1 to 10 n = 0 for i in range(10): n = n + 1 abundant(n) Hope this helps!
3.046875
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Many electronic systems employ programmable gain amplifiers as a basic analog building block. An example of a conventional programmable gain amplifier (800) is illustrated in FIG. 8. Programmable gain amplifier 800 includes an operational amplifier (AMP), three resistors (R81-R83), and two switches (S81-S82). The operational amplifier includes a non-inverting input terminal (INP), an inverting input terminal (INM), and an output terminal (AOUT). Switch S81 is connected between AOUT and node N81. Switch S82 is connected between AOUT and node N82. Resistor R81 is connected between node N81 and INM. Resistor R82 is connected between node N82 and INM. Resistor R83 is connected between INM and a circuit ground (GND). In operation, operational amplifier AMP is configured to receive an input signal (e.g., IN) at the non-inverting input (INP), and provide an output signal (e.g. OUT) at the output terminal (AOUT) that is related to the input signal according to a gain scaling factor (X). The gain scaling factor (X) is determined by the impedance in the feedback path between the output (OUT) and the inverting input (INM). Switches S81 and S82 are arranged to change the selection of the feedback components (resistors R81 and R82) to adjust the gain scaling factor (X). The selected feedback component is resistor R81 when switch S81 is closed, while the selected feedback component is resistor R82 when switch S82 is closed. The relationship between the input signal (IN) and the output signal (OUT) is determined by the feedback components and the switches as follows: OUT=IN*(1+X), where X is determined by the feedback components. In one example, X=R81/R83 when switch S1 is closed and switch S2 is open. In another example, X=R82/R83 when switch S2 is closed and switch S1 is open.
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Schizaea dichotoma Schizaea dichotoma, the branched comb fern is a small plant usually found in open forest or heath, often on sandy soils. The habit is mostly upright, with up to 20 segments, twice or more times branched. Found in Australia, New Zealand, Papua New Guinea, Malesia and islands in the Pacific Ocean. A low plant, 20 to 40 cm tall. The specific epithet dichotoma is derived from Greek, meaning "twice cut", referring to the branched nature of the fronds. This plant first appeared in scientific literature in the year 1753 as Acrostichum dichotomum, published in the Species Plantarum by Carl Linnaeus. References Category:Schizaeales Category:Flora of Australia Category:Flora of New Zealand Category:Flora of New Caledonia Category:Flora of Malesia Category:Flora of Indonesia Category:Flora of New Guinea Category:Plants described in 1753
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The regular polygon shown here has 6 congruent sides and 6 congruent interior angles. Two of the sides are extended until they meet at point A. What is the measure of angle A? A. 160 degreesB. 120 degreesC. 72 degreesD. 60 degreesE. 35 degrees Answers and explanations The correct answer is Choice (A). To find the sum of the interior angles of a polygon, you use this formula: where n is the number of sides in the polygon. If you can’t remember that formula, simply divide the shape into triangles. The sum of the interior angles in each triangle measures 180 degrees, so for each triangle add 180 degrees and you get the sum of all the angles in the polygon. The polygon in this problem has 4 sides, so you know its interior angles add up to 360 degrees. The problem tells you that the sum of angles a and b is more than 70 degrees. The lowest possible value for a + b is 71 degrees. If at its lowest, then at its highest. That means that The answer that states c + d < 290 is Choice (A). Double-check the rest of the information to make sure Choice (A) is the right answer. The problem says that a + b < 150. If a + b < 150, then its highest value is 149 degrees; the lowest the sum of c and d can be is 360 – 149 = 211. Choice (A) works. The correct answer is Choice (D). The formula for finding the interior angle measures of a regular polygon is as follows, where n represents the number of sides in the polygon: Apply the formula to the figure in the question to find the measure of each interior angle in the polygon: So each angle in the hexagon measures 120 degrees. The angles in the triangle that’s formed by the two extended sides must each be 60 degrees because two of those angles form a straight line with the two 120-degree angles in the hexagon and 180 – 120 = 60. If two angles in a triangle each measure 60 degrees, the third angle, angle A, must also measure 60 degrees.
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Introduction ============ The World Health Organization (WHO) defines adherence as "The extent to which a person's behavior -- taking medication, following a diet, and/or executing lifestyle changes, corresponds with agreed recommendations from a health care provider."[@b1-ppa-4-001] Adherence to treatment regimes is essential to ensure patients receive the maximum benefit from their treatment and also to make sure that treatment is cost-effective. Nonadherence or poor adherence to therapy can lead to poor outcomes or treatment failure, and to increased costs.[@b1-ppa-4-001] The WHO considers poor adherence to medication to be a serious problem worldwide. In developed countries, adherence among patients suffering from chronic diseases is as low as 50%. This figure is probably even lower in developing countries.[@b1-ppa-4-001] For example, adherence to oral anticancer agents can be as low as 20%,[@b2-ppa-4-001] and adherence to some oral treatments for diabetes is only 36%.[@b3-ppa-4-001] This article will explore the issue of adherence to treatment for multiple sclerosis (MS). The barriers to full adherence encountered by patients and clinicians will be described, and strategies that may be used to improve rates of adherence will be discussed. Adherence to MS therapy ======================= MS is a chronic demyelinating autoimmune disorder of the central nervous system. It is estimated to affect 2.5 million people worldwide, and is the most common cause of neurological disability among young people.[@b4-ppa-4-001] MS has several clinical forms. Patients are most often initially diagnosed with relapsing--remitting MS with new symptoms appearing during discrete acute attacks (relapses) between which the patient regains some or all neurological function, although residual disability tends to accumulate over time. Many patients with relapsing--remitting MS go on to develop secondary progressive MS, which is characterized by progressive neurological decline, over which acute relapses may be superimposed.[@b5-ppa-4-001] MS is currently incurable, although a variety of treatment approaches are available, including physiotherapy, psychotherapy, and management strategies to mitigate the symptoms of MS. Immunomodulatory agents are available that can modify the course of the disease by altering the pathological immune responses underlying MS. Treatment with these disease-modifying drugs (DMDs) aims to reduce the rate of acute neurological attacks, and can delay disability progression. First-line treatment options for MS currently consist of four immunomodulatory drugs: interferon (IFN) beta-1a, administered subcutaneously (sc) 3 times weekly; IFN beta-1a, administered intramuscularly (im) once weekly; IFN beta-1b administered sc every other day; and glatiramer acetate administered sc once daily. All of these drugs have to be administered parenterally on a regular basis, and are associated with injection-related side-effects such as injection-site reactions, which may influence adherence, particularly during the first few months of treatment. The second line of treatment for MS includes immunosuppressant agents such as cyclophosphamide and mitoxantrone. While these agents have been shown to be effective in MS therapy, they have widespread effects on the immune system and suppress both beneficial and harmful immune responses.[@b6-ppa-4-001] These drugs tend to be used only in patients who do not respond to first-line therapy, and potential toxicity issues make them a short-term option. Natalizumab is a newer immunosuppressant, which has a more targeted activity against pathological immune responses. Again, because of the potential for serious side-effects, natalizumab is generally only recommended for patients with highly active MS who show an inadequate response to first-line therapy.[@b7-ppa-4-001] Studies of adherence to MS therapy in clinical practice have shown that patients are most likely to discontinue therapy within the first 6 months after treatment initiation. Discontinuation rates during the first 6 months of treatment have been reported to range from 9% to 20%,[@b8-ppa-4-001],[@b9-ppa-4-001] although abandonment of an MS treatment regimen can happen at any time. In one study of patients with relapsing--remitting MS, with a mean follow-up duration of 4.2 years, 46% of patients stopped treatment over the course of the study.[@b10-ppa-4-001] Rates of discontinuation of therapy in clinical trials tend to be somewhat lower than in clinical practice, perhaps reflecting the fact that patients enrolled in trials receive more thorough follow up than is usual in everyday practice.[@b8-ppa-4-001] In general, clinical trials of DMDs in MS show favorable rates of adherence, particularly the more recent trials, which routinely employ management strategies to minimize adverse events (AEs) and to ensure patients' compliance with treatment. However, dropout rates from clinical trials may not give an accurate picture of long-term adherence to therapy in the clinical setting, where the patient and physician may elect to change to a different drug, or the patient may choose to discontinue therapy altogether. Additionally, disease management strategies employed as standard practice vary between clinics, and this may cause adherence rates to differ between centers. Barriers to adherence to MS treatment ===================================== Disease-related factors ----------------------- A patient's subtype of MS may influence their likelihood of adherence to therapy. One study, which followed 632 patients for a mean period of 47.1 months, found that adherence was poorer in patients with secondary progressive MS than in those with relapsing--remitting MS. The authors also noted that the patients with relapsing--remitting MS who stopped therapy were younger than those who remained on treatment, had higher levels of initial disability and more active disease, and were more likely to be female.[@b11-ppa-4-001] Cognitive impairment and depression ----------------------------------- Cognitive impairment often results from MS,[@b12-ppa-4-001] and may make it difficult for the patient to follow correctly the prescribed treatment regimen. Current MS therapies require regular administration, and impaired memory function may reduce the likelihood of timely administration. Additionally, despite efforts to simplify the injection process through the design of delivery technology, cognitive dysfunction could also impair correct injection technique. However, the impact of cognitive impairment on adherence to MS therapy remains to be clarified in studies. Depression is common among patients with MS, and may negatively affect adherence. A study of patients with MS initiating IFN beta-1b therapy found that 41% of patients reported new or increased depression within 6 months of starting treatment. Eighty-six percent of patients who received psychotherapy or antidepressant treatment continued therapy, compared with 38% of patients who received no treatment for depression (*P* = 0.003).[@b13-ppa-4-001] Efficacy concerns ----------------- Perceived lack of efficacy is one of the most commonly cited reasons for treatment discontinuation.[@b8-ppa-4-001],[@b11-ppa-4-001],[@b14-ppa-4-001] The disease course of MS varies between patients, and while therapy is often effective, the individual patient may not fully understand the benefits of remaining on treatment. The effects of treatment may not become apparent immediately, which may in part explain the high discontinuation rates observed in the first few months of treatment. Additionally, the unpredictability of the disease course means it is impossible to predict how their MS would affect them were they not on treatment, so the true benefit of treatment in the individual patient is unclear. Some patients starting MS therapy tend to be overly optimistic about the benefits of therapy. Unrealistic expectations have been shown to be highly predictive of premature discontinuation. Therefore, it is important that patients' expectations are managed prior to treatment initiation.[@b9-ppa-4-001],[@b15-ppa-4-001] Importantly, if a patient does not adhere to the prescribed treatment regimen, they may experience poorer outcomes, lose faith in their treatment, and become even more likely to be poorly adherent. Adverse events -------------- AEs associated with MS therapy may also contribute to non-adherence to treatment regimens. The incidence of AEs associated with MS therapy tends to decrease the longer a patient is on therapy. Therefore, long-term adherence to treatment is more likely to be achieved if patients remain on treatment through the initial period when AEs can be particularly problematic. Management strategies to minimize the impact of AEs are therefore imperative to preserve adherence. One of the most common AEs associated with IFN beta therapy is flu-like symptoms.[@b16-ppa-4-001] These symptoms tend to appear early in the treatment course, then diminish in frequency and severity with increased time on treatment. For example, in the pivotal trial of sc IFN beta-1a, flu-like symptoms were reported by 69% of patients receiving IFN beta-1a over years 1 to 4, but by only 12% after up to 8 years of follow up.[@b17-ppa-4-001],[@b18-ppa-4-001] Injection-site reactions (ISRs) are another commonly reported AE associated with MS therapies. The incidence and severity of such reactions may vary between treatments.[@b8-ppa-4-001] Injection-site necrosis can occur with IFN beta treatment, and is very rarely seen with glatiramer acetate.[@b19-ppa-4-001]--[@b21-ppa-4-001] However, glatiramer acetate injection can sometimes cause lipoatrophy at the application site, leading to, sometimes permanent, disfigurement.[@b22-ppa-4-001],[@b23-ppa-4-001] Correct injection technique and rotation of injection sites can help to avoid ISRs.[@b24-ppa-4-001] Inconvenience and needle phobia ------------------------------- Aside from the AEs associated with MS therapies, some patients also find the process of regular self-injection burdensome, and adherence can be compromised as a result. Furthermore, physical disability and cognitive impairment resulting from MS can make self-injection and ability to comply with treatment regimens difficult.[@b25-ppa-4-001] Needle phobia, which is experienced by up to 22% of the general population, can also be a significant barrier to self-administration of parenteral therapies among patients with MS.[@b26-ppa-4-001] Studies in other therapy areas have shown that a complex regimen and frequent dosing schedule can be barriers to adherence.[@b27-ppa-4-001] Currently, all first-line therapies for MS require parenteral administration weekly (in the case of im IFN beta-1a) or more frequently. In the case of glatiramer acetate,patients are required to inject daily. It may be speculated that patients with MS would be more adherent to drugs requiring less-frequent administration. Natalizumab is delivered via a monthly intravenous infusion. It could be argued that the dosing frequency and the fact that natalizumab is administered during a clinic visit could encourage adherence. Conversely, this route of administration may be considered inconvenient by some patients. Discontinuation patterns and consequences of poor adherence =========================================================== Discontinuation tends to occur earlier after treatment initiation if the reason for stopping therapy is AEs than when discontinuation is due to lack of efficacy. In a study of discontinuation patterns in patients receiving IFN beta, patients who stopped therapy as a result of AEs did so after a median period of 13 months on treatment, whereas those who discontinued as a result of treatment failure (defined as non-reduction in pre-treatment relapse rate and/or sustained increase of Expanded Disability Status Scale score of ≥ 1 point) did so after a median period of 35 months (*P* = 0.0004; Mann--Whitney test).[@b28-ppa-4-001] In MS, it is currently unclear precisely what effect the degree to which patients adhere to therapy has on clinical or magnetic resonance imaging outcomes, but patients who do not adhere to therapy are unlikely to receive the full potential benefit of treatment,[@b8-ppa-4-001] and therefore may be at increased risk of poorer outcomes. A study that investigated the relationship between the duration of gaps in MS treatment regimens and the incidence of severe MS relapses found that patients who had gaps in therapy lasting ≥90 days had a nearly twofold greater probability of experiencing a severe relapse than patients with shorter gaps in therapy.[@b29-ppa-4-001] This shows the importance of adherence to prescribed regimens for MS. Potential barriers to treatment adherence in MS are summarized in [Figure 1](#f1-ppa-4-001){ref-type="fig"}. All of these issues can affect the patient's quality of life, whether they relate to features of the disease, or to the treatment itself. It may be speculated that poor overall quality of life may affect the individual patient's likelihood of adherence to therapy. Management strategies to enhance adherence ========================================== Maximizing adherence to MS therapies to improve a patient's chance of gaining the full benefit from their treatment is an important therapeutic goal. Patient education is of paramount importance in achieving this, as a patient's commitment to a therapeutic regimen may well depend on their understanding of their condition, their need for treatment, and the potential benefits of treatment.[@b15-ppa-4-001] As perceived lack of efficacy can be a barrier against adherence, patients need to have realistic expectations of their treatment, and again, information can enhance the likelihood of good adherence. A study that examined patients' expectations of treatment before beginning IFN beta therapy found that 57% of patients had unrealistic expectations about reduction in relapse rate.[@b9-ppa-4-001] Although educational procedures significantly altered unrealistic expectations, 36% of patients still had unrealistic expectations of therapy after education. Of those patients who discontinued IFN beta therapy, 64% had unrealistically optimistic post-education expectations of treatment.[@b9-ppa-4-001] Patients should be informed of therapeutic options, the potential benefits and risks of each treatment and the importance of adhering to their given treatment regimen. Allowing patients to take an active role in treatment decisions may make them feel empowered, which, in turn, could enhance their motivation to remain adherent. Patients also benefit from receiving information about potential side-effects, and how these can be managed.[@b15-ppa-4-001] AEs may occur with MS therapies, but they can be managed so as to minimize the impact on the patient's life. As all DMDs for MS require frequent injections, ISRs and pain may be experienced. Suitable injection technique can minimize these events and thus enhance adherence. Appropriate injection procedures include those outlines below. Refrigerated medication should be warmed to room temperature before administration.Hands should be washed thoroughly prior to injection.The injection site should be thoroughly cleansed but completely dry before the injection.Ice should not be applied to the skin before injection, but may be used afterwards.The needle should be inserted perpendicularly to the skin and completely penetrate the skin.For im injections, shorter needles should be used for patients with less subcutaneous fat.The patient should avoid smoking.Auto-injector use is recommended.Rotation of injection sites is vital to minimize reactions due to repeated, frequent injections.The use of topical steroid preparations is not recommended. The use of auto-injector devices to administer DMDs has been shown to reduce the incidence of ISRs compared with manual injection.[@b30-ppa-4-001] These devices are also convenient to use, and may be particularly beneficial for patients with poor manual dexterity.[@b31-ppa-4-001] As needle phobia can be a barrier to adherence to injectable therapies,[@b26-ppa-4-001] a device in which the needle is hidden from view may have the additional benefit of reducing anxiety and thus improving adherence. Many patients treated with IFN beta experience flu-like symptoms, particularly during the few months after treatment is started. Dose titration at initiation of IFN beta treatment is commonly employed to minimize the incidence of flu-like symptoms. A useful scheme for the titration of IFN beta treatment is to begin with 25% of the full dose for the first week, 50% in the second, and if this is well tolerated, the full dose is given from the third week onwards.[@b16-ppa-4-001] Concomitant non-steroidal anti-inflammatory drug (NSAID) treatment, either prophylactically or as required, can also help to reduce these symptoms.[@b16-ppa-4-001] Low doses of corticosteroids may be administered to patients who do not respond satisfactorily to NSAIDs for flu-like symptoms. A randomized study compared the efficacy of corticosteroids, ibuprofen, and acetaminophen for the control of IFN beta-related flu-like symptoms. The three treatments showed a similar degree of efficacy on flu-like symptoms, although flu-like symptoms immediately following injection were less severe in patients treated with ibuprofen.[@b32-ppa-4-001] Another technique for the management of flu-like symptoms is for patients to administer their therapy in the evening, meaning that the majority of acute symptoms occur while they are asleep.[@b16-ppa-4-001] Adherence to MS therapy can be enhanced by providing the patient with a support network. Often, the MS nurse is well placed to co-ordinate the support network, being the central point of contact with the patient once therapy has been initiated. MS nurses can provide the patient with information on available support services offered by the clinic or in the community. Many patients find that self-help groups can provide valuable support and information. Additionally, the MS nurse can advise the patient on the management of symptoms, side-effects, and co-morbidities. In addition to the care provided by the physician and nurse, treatment, information, and support from a wider, multidisciplinary team can enhance further the patient's adherence to therapy.[@b33-ppa-4-001] The patient and their family and friends are central in this care model, with support from the family practitioner, physiotherapist, neuropsychologist, and MS societies forming valuable relationships with the patient. Many patients report that how they are treated by their care team influences their likelihood of following medical recommendations.[@b33-ppa-4-001] One study of adherence to IFN beta-1b in 939 patients with SPMS found that the highest rates of adherence were achieved in clinics where empathetic and less formal relationships between patients and caregivers were encouraged.[@b34-ppa-4-001] Effective and sensitive working relationships between the patient and their support team are an important part of the patient's care. As the disease course of MS is unpredictable, and the patient's attitudes and behavior patterns can be changeable, encouraging adherence is a complex issue. The support team needs to be aware of the potential barriers to adherence and sensitive to the patient's state of mind in order to support the patient with the goal of maintaining adherence.[@b35-ppa-4-001] The formulation of MS drugs can influence their tolerability, and formulation adjustments may serve to improve tolerability and so enhance adherence. For example, IFN beta-1a for sc injection has been re-formulated, produced without fetal bovine serum and without human serum albumin as an excipient. A recent 2-year study[@b36-ppa-4-001] compared data on the tolerability and immunogenicity of patients treated with the new formulation of sc IFN beta-1a (n = 260) with historical data on patients treated with the previous formulation of sc IFN beta-1a in the EVIDENCE (n = 339) and REGARD (n = 381) trials. The incidence of ISRs in patients receiving the new formulation was 31%, almost three times lower than in the EVIDENCE study (86%), and lower than in the REGARD study (41%). Levels of immunogenicity were lower with the new formulation than in the historical cohort, with apparent comparable efficacy. However, it remains to be seen whether these improvements in tolerability and immunogenicity will translate into higher adherence rates. A study that assessed the immunogenicity and safety of a human serum albumin-free formulation of im IFN beta-1a found the tolerability profile of the human serum albumin-free formulation similar to that of the original formulation.[@b37-ppa-4-001] Future directions for the enhancement of adherence in MS ======================================================== There are several strategies being explored that may prove to enhance adherence to MS therapies. These include advances in delivery technology, improved patient education and support programs and alternative routes of administration. Perhaps the most important advance in MS treatment that is anticipated to significantly improve adherence to long-term treatment will be the availability of orally administered drugs. In terms of adherence, oral drugs have a potential advantage over injected therapies in that needle phobia and injection-related AEs will not be an issue, making treatment available to patients with MS who are unable, or unwilling, to receive regular injections. Nonparenteral routes of drug administration can also be expected to enhance adherence.[@b1-ppa-4-001] In other therapy areas, such as oncology and diabetes, patients prefer receiving their medication in the form of tablets or an inhaled preparation, rather than as injections.[@b38-ppa-4-001]--[@b40-ppa-4-001] Additionally, oral or inhaled medications are associated with heightened levels of patient satisfaction with their treatment.[@b38-ppa-4-001],[@b41-ppa-4-001] Therefore, with the more convenient administration route, oral MS therapies may be expected to improve rates of adherence compared with those found with injected drugs. Although the development of new oral agents for the treatment of MS is an important step in improving adherence to MS therapy, oral administration may not entirely solve the problem of poor adherence. The example of osteoporosis treatment clearly shows that frequency of dosing can greatly influence the adherence to oral therapies. Studies show that persistence with weekly oral bisphosphonate therapy is substantially greater than with a daily regimen, although still not optimal. Additionally, patient surveys show that the majority of patients prefer a weekly regimen to daily, with a once-monthly regimen being the most popular.[@b42-ppa-4-001] Studies in other therapy areas have also shown that simpler[@b43-ppa-4-001],[@b44-ppa-4-001] and less frequent[@b45-ppa-4-001],[@b46-ppa-4-001] dosing produces greater adherence than more frequent administration. Several oral agents for the treatment of MS are currently being studied in Phase III trials ([Table 1](#t1-ppa-4-001){ref-type="table"}). Laquinimod, a derivative of linomide, alters dendritic cell responses and promotes a shift to Th2 immunity.[@b47-ppa-4-001] BG-12 is a second-generation fumaric acid derivative, which has shown promising results on MRI measures of MS in Phase II studies.[@b48-ppa-4-001] Fingolimod (FTY720) is a sphingosine-1-phosphate agonist that was originally investigated for the prevention of renal transplant rejection. It is an immunosuppressive agent that induces lymphopenia by sequestering lymphocytes into secondary lymph nodes. Via this mechanism it prevents T cells from crossing the blood-brain barrier and invading the CNS. Fingolimod preferentially depletes B cells and may have vasoprotective properties and neuroprotective effects. Phase II trials of fingolimod in patients with MS showed efficacy in MRI and clinical measures.[@b49-ppa-4-001] Preliminary results of a Phase III study indicate that the efficacy of fingolimod is superior to that of im IFN beta-1a for relapse rate.[@b50-ppa-4-001] Leflunomide is used in the treatment of rheumatoid arthritis. Its active metabolite, teriflunomide, reduced the number of MRI lesions in patients with MS in Phase II trials. It causes the selective depletion of B and T cells by inhibiting the synthesis of pyrimidine nucleotides.[@b51-ppa-4-001] Cladribine is a small molecule, which acts as a prodrug: a deoxyadenosine analogue immunomodulator that is resistant to deamination by the enzyme adenosine deaminase. Activation of cladribine in specific cell types results in preferential reduction of lymphocyte B and T subtypes,[@b52-ppa-4-001],[@b53-ppa-4-001] both of which are involved in MS pathogenesis,[@b54-ppa-4-001],[@b55-ppa-4-001] with relatively minor effects on other hematological and immune cell types.[@b52-ppa-4-001],[@b56-ppa-4-001]--[@b58-ppa-4-001] Cladribine tablets therapy was developed following encouraging clinical trial experience with parenteral cladribine in MS.[@b52-ppa-4-001],[@b56-ppa-4-001],[@b59-ppa-4-001] The sustained effects on T and B cells has allowed for the development of cladribine tablets using a short-course annual dosing regimen. This may mean that patients need to take tablets for 10 or 20 days per year. Cladribine tablets recently became the first orally administered investigational treatment for MS to complete a 2-year Phase III pivotal study in which it demonstrated rapid and significant improvements in clinical outcome measures, including reductions in relapse rates and the risk of developing 3-month sustained disability progression relative to placebo in patients with relapsing--remitting MS.[@b60-ppa-4-001]--[@b62-ppa-4-001] Should one or more of these oral therapies in development be approved for the treatment of MS, it may be speculated that their benefits would lead to higher levels of treatment adherence currently seen with parenteral treatments. While a change in administration route is unlikely to completely solve the problem of poor adherence, the advent of oral therapies represents a significant milestone in the care of patients with MS. Conclusions =========== Adherence to treatment regimens is essential for patients to gain the full benefit of their therapies.[@b1-ppa-4-001] Although the impact of non-adherence to MS therapies has not been widely assessed, it is reasonable to assume that poor adherence to MS drugs results in poorer outcomes. It has been shown that long interruptions in MS therapy confer a higher risk of severe relapse.[@b29-ppa-4-001] As with other chronic diseases such as cancer and diabetes, nonadherence and poor adherence to therapy are common in MS, and improving adherence should be recognized as an important treatment goal in its own right. Many factors can cause patients to discontinue treatment, including treatment-related AEs and patient perception of lack of efficacy. Where possible, these should be addressed through patient education and support, and strategies to maximize drug tolerability to improve adherence. Appropriate measures to enhance adherence are summarized below. Adherence must be considered an important modifier of the efficacy of long-term treatment.The management of patients' expectations should be central in the process of treatment of patients with MS.Patients should be trained in appropriate injection technique (such as rotation, self-injection).Patients must be informed of the potential side-effects and on the correct management of the latter.Specific work must be done with non-adherent patients, and the possibility of switching to a different therapy, if appropriate, should be discussed. Oral therapies currently in development also have the potential to improve adherence: the absence of ISRs and ease of administration may make these treatments more acceptable to patients, particularly if the tablet burden is low. While suboptimal adherence to MS therapies remains a problem, adherence can be enhanced by various strategies. Future developments in drug and administration technology may be expected to further improve adherence, and therefore patient outcomes. The author takes full responsibility for the content of the paper but thank Steve Smith, Caudex Medical (supported by Merck Serono S.A. -- Geneva, Switzerland, an affiliate of Merck KGaA, Darmstadt, Germany), for his assistance in preparing the initial draft. **Disclosures** The author has received financial support for research activities from the University of Catania and has also received fees from Merck Serono S.A. -- Geneva, Switzerland, an affiliate of Merck KGaA, Darmstadt, Germany and Sanofi-Aventis, as well as fees from Bayer Schering Pharma for speaking services. The author takes full responsibility for the data, the analyses and the interpretation, and the conduct of the research; had full access to the data; and has the right to publish any and all data, separate and apart from the attitudes of the sponsor. ![Factors leading to poor adherence to multiple sclerosis therapy.](ppa-4-001f1){#f1-ppa-4-001} ###### Oral agents currently in Phase III trials for multiple sclerosis **Agent** **Molecule type** **Therapeutic target** **Current/previous use** **Expected dosing regimen** --------------- -------------------------------------------------- ------------------------------------------------------- ------------------------------------------------- ---------------------------------------------------------------------------- Fingolimod Partial sphingosine-1-phosphate receptor agonist Lymphocyte trafficking Renal transplantation (failed Phase III trials) 5.0 or 1.25 mg daily Laquinimod Derivative of linomide (roquinimex) Prevention of T-cell activation Oncology (antiangiogenic agent) 0.6 mg daily BG-12 Fumaric acid derivative Prevention of T-cell activation Psoriasis (approved in Germany) 720 mg daily Teriflunomide Active metabolite of leflunomide Lymphocyte antiproliferation agent Rheumatoid arthritis 7.0 or 14.0 mg daily Cladribine Purine nucleoside analog pro-drug Preferential reduction of T and B lymphocyte subtypes Hairy cell leukemia and lymphoma Short-course annual dosing regimen (3.5 mg/kg or 5.25 mg/kg over 96 weeks)
3.078125
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Q: How to represent a number greater than the maximum value How to represent values that exceed the max values of any particular data type (int, long ) ? I am thinking of having another storage space acting like a counter. Once the max value is crossed, the counter updates to say , the variable has exceeded the limit for "x" number of times. Is there some other efficient way of doing it ? How do we display the exact value ? P.S : Just a hypothetical question. A: One way is to actually carve out one of the values for this purpose. For example, if you have a 16-bit integral type that can represent the values from 0 through 65535 inclusive, reduce the range to 0 through 65534 and use 65535 to represent the value "too darned big". You would have to be careful to control the operations so that they wouldn't produce that value in the normal course of events but that's reasonably easy if your language provides class capabilities. Alternatively, you can use the next biggest data type such as long for int or long long for long and use the extra range to store information. And, if you need more than that, you can code up a bignum library (or use one that already exists) so that there are no artificial limits placed on your numbers.
3
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Gross motor skill Gross motor skills are the abilities usually acquired during childhood as part of a child's motor learning. By the time they reach two years of age, almost all children are able to stand up, walk and run, walk up stairs, etc. These skills are built upon, improved and better controlled throughout early childhood, and continue in refinement throughout most of the individual's years of development into adulthood. These gross movements come from large muscle groups and whole body movement. These skills develop in a head-to-toe order. The children will typically learn head control, trunk stability, and then standing up and walking. It is shown that children exposed to outdoor play time activities will develop better gross motor skills. Types of motor skills Motor skills are movements and actions of the muscles. Typically, they are categorized into two groups: gross motor skills and fine motor skills. Gross motor skills are involved in movement and coordination of the arms, legs, and other large body parts and movements. Gross motor skills can be further divided into two subgroups of locomotor skills and object control skills. Gross locomotor skills would include running, jumping, sliding, and swimming. Object control skills would include throwing, catching and kicking. Fine motor skills are involved in smaller movements that occur in the wrists, hands, fingers, and the feet and toes. They participate in smaller actions such as picking up objects between the thumb and finger, writing carefully, and even blinking. These two motor skills work together to provide coordination. Less developed kids focus on their gross movements, while more developed kids have more control over their fine movements. Development of posture Gross motor skills, as well as many other activities, require postural control. Infants need to control the heads to stabilize their gaze and to track moving objects. They also must have strength and balance in their legs to walk. Newborn infants cannot voluntarily control their posture. Within a few weeks, though, they can hold their heads erect, and soon they can lift their heads while prone. By 2 months of age, babies can sit while supported on a lap or an infant seat, but sitting independently is not accomplished until 6 or 7 months of age. Standing also develops gradually across the first year of life. By about 8 months of age, infants usually learn to pull themselves up and hold on to a chair, and they often can stand alone by about 10 to 12 months of age. There is a new device called a “Standing Dani” developed to help special needs children with their posture. Learning to walk Walking upright requires being able to stand up and balance position from one foot to the other. Although infants usually learn to walk around the time of their first birthday, the neural pathways that control the leg alternation component of walking are in place from a very early age, possibly even at birth or before.[1] This is shown because 1- to 2-month-olds are given support with their feet in contact with a motorized treadmill, they show well-coordinated, alternating steps. If it were not for the problem of switching balance from one foot to the other, babies could walk earlier. Tests were performed on crawling and walking babies where slopes were placed in front of the path and the babies had to decide whether or not it was safe. The tests proved that babies who just learned how to walk did not know what they were capable of and often went down slopes that were not safe, whereas experienced walkers knew what they could do. Practice has a big part to do with teaching a child how to walk. Vision does not have an effect on muscle growth but it could slow down the child’s process of learning to walk. According to the nonprofit Blind Children Center, “Without special training, fully capable infants who are visually impaired may not learn to crawl or walk at an appropriate age and gross and fine motor skills will not properly develop.” When the child is not able to see an object then there is no motivation for the child to try to reach for it. Therefore, they do not want to learn independently. Learning to walk is done by modeling others and watching them. Children when put in environments with older children will observe and try and copy the movements done. This helps the child learn through trial and error. The babies will imitate others, picking up the skills a lot faster than creating their own errors. Visually impaired children may need physical therapy to help them learn these gross motor skills faster. One hour of therapy each week is not enough so parents have to make sure they are involved in this process. The parent can help by telling the baby the direction of where the object is and encourage them to get it. You must have patience because every child has their own developmental schedule and it is even truer for the children with special needs. Focusing on the progress of your child is better than focusing on comparing your child to other children. (Humphrey) Infancy development It has been observed by scientists that motor skills generally develop from the center to the body outward and head to tail. Babies need to practice their skills; therefore they will grow and strengthen better. They need space and time to explore in their environment and use their muscles. “Tummy-time” is a good example of this. At first they are only able to lay their belly on the floor but by around two months they start to gain muscle to raise their head and chest off the ground. Some are also able to go on their elbows. They will also start to kick and bend their legs while lying there, this helps to prepare for crawling. By four months they are able to start to control their head and hold it steady while sitting up. Rolling from belly to back movements is started. At about five months the baby will start to wiggle their limbs to strengthen crawling muscles. Infants can start to sit up by themselves and put some weight on their legs as they hold onto something for support by six months. As they enter their first-year caregivers needs to be more active. The babies will want to get into everything so the house needs to become ‘baby proofed’. Babies are able to start to reach and play with their toys too. It is said that the use of baby walkers or devices that help to hold the baby upright are said to delay the process of walking. Research has been found that it delays developing the core torso strength, which can lead to different issues down in their future. Around ten months they should be able to stand on their own. Throughout their years of life different motor skills are formed. (Oswalt) With regards to the gait pattern, study shows that infant at 12 months old exhibit larger mediolateral motion, which may be caused by weak muscle strength and lack of stability. They also show a synchronized use of hip and shoulder while they are walking, which is different from a mature gait pattern performed by adults. The ankles didn't move as much among 12-month infants as compared to that of adults performing a mature walking. Development in the second year Development in the second year of life, toddlers become more motorically skilled and mobile. They are no longer content with being in a playpen and want to move all over the place. Child development experts believe that motor activity during the second year is vital to the child's competent development and that few restrictions, except for safety, should be placed on their motoric adventures. By 13 to 18 months, toddlers can move up and down steps and carry toys. Once they reach the top of the stairs though, they are not able to get back down. They also begin to move from one position to another more smoothly. (Oswalt) Significant changes in gait patterns are also observed in the second year. Infants in the second year have a discordant use of hip and shoulder while walking, which is closer to an adult walking pattern. They are also able to utilize the rage of motion of their ankles, toes, and heels more, which is similar to a mature walk. By 18 to 24 months, can move quicker or run for a short distance along with other motor skills. They also start to walk backwards and in circles and begin to run. They can also not only walk up the stairs with their hands and feet but are now able to hold onto the handrail and walk up. Near the end of their second year, complex gross motor skills begin to develop including throwing and kicking. Their skills becomes more natural. Pedaling a tricycle and jumping in place is acquired. At the end they are very mobile and can go from place to place. It is normal for them to get themselves into small situations that could be dangerous such as walking into the street because their brain can’t send the information fast enough to their feet. Parents need to keep an eye on their children at all times. (Oswalt) In a majority of the select kinematic and kinetic variables, there are greater differences between two-year-old children and four-year-old-children than there are between four year old children and six year old children. The variables for which there were significant differences tended to be in displacement, velocity, and magnitude of force measurements. In a majority of the select kinematic and kinetic variables, there are greater differences between two-year-old children and four-year-old-children than there are between four year old children and six year old children. The variables for which there were significant differences tended to be in displacement, velocity, and magnitude of force measurements. Development of children with disabilities Children with disabilities who are as young as seven months can learn to drive a power wheelchair. This will give specific benefits to the leg, is paralyzed. This chair may decrease the rate of development of the child’s gross motor skills, but there are ways to compensate for this. These children usually work with a physical therapist to help with their leg movements. Walkers and other devices are used to help aide this process and avoid obstacles. The negative side to this is that they are limited in their mobility. There is research out to find a device to encourage children to explore their environment while gaining their gross motor skills. This will also hopefully help them with their exercise. Childhood Early childhood is a critical period for the development of fundamental motor skills. As a preschooler, the child develops depending on his/her interactions with the surrounding environment. If the child is in an encouraging environment with constructive feedback, he or she will develop fundamental motor skills at a faster rate. Typically, females perform better fundamental movement skills at an earlier age than males. Although many studies prove this to be true, it is dominantly true in walking. Girls typically go through maturity faster than boys do, causing them to also be less active. This allows boys to be deemed more active, due to the fact that they mature much later than their opposing gender. However, this does not give a clear answer as to whether or not girls learn to walk before boys. One would think that learning to walk sooner would allow for a higher activity level, though since girls have a noticeably lower activity level than boys, one would assume that this would mean that girls would learn to walk after boys. But since they mature earlier, that would involve the walking stage. As they grow older, children become more proficient in their tasks allowing them to use their high developed skill for events such as sports where these motor skills are highly required. Children who do not master fundamental motor skills are less likely to participate in sport games during childhood and adolescence. This is one explanation of why boys tend to be more or less athletic than their opposite gender. Children at a younger age might not be able to perform at the level of older children, but their ability to learn and improve on motor skills is much higher. At 3 years of age, children enjoy simple movements, such as hopping, jumping, and running back and forth, just for the sheer delight of performing these activities. However, the findings in the article "The relationship between fine and gross motor ability, self-perceptions and self-worth in children and adolescents" it stated that there was not a statistical significance in athletic competence and social competence. This correlation coefficient was .368 and simply means that there is a low correlation between those two relationships. A child being able to perform certain gross and fine motor skills does not mean that they will have the ability to demonstrate social skills such as conversation, social awareness, sensitivity, and body language. This Their body stability is focused on the child's dynamic body base and is related to their visual perceptions such as height, depth, or width. A study was done to assess motor skill development and the overall rate and level of growth development. This study shows that at the preschool age children develop more goal-directed behaviors. This plays a big role, because their learning focuses around play and physical activity. While assessing the gross motor skills in children can be challenging, it is essential to do so in order to ensure that children are prepared to interact with the environment they live in. Different tests are given to these children to measure their skill level. At age 4, children continue to do the same actions as they did at age 3, but further their moving. They are beginning to be able to go down the stairs with one foot on each step. At 5 years of age, they are fully able to go down the stairs one foot at a time in addition to improvements in their balance and running. Their body stability becomes more mature and their trunk is fixed on their posture. Performances are more fluent and are less influenced by factors such a slope and width. During middle and late childhood, children's motor development becomes much smoother and more coordinated than it was in early childhood. As they age, children become able to have control over their bodies and have an increased attention span. Having a child in a sport can help them with their coordination, as well as some social aspects. Teachers will suggest that their students may need occupational therapists in different situations. Students could get frustrated doing writing exercises if they are having difficulties with their writing skills. It also may affect the teacher because it is illegible. Some children also may have reports of their “hands getting tired”. There are many occupational therapists out there today to give students the help they need. These therapists were once used when something was seriously wrong with your child but now they are used to help children be the best they can be. In the Article "The Relationship Between Fundamental Motor Skills and Outside-School Physical Activity of Elementary School Children" we can see that the developmental level of overhand throwing and jumping of elementary kids is related to skill specific physical activity outside of school. In the studies done boys were seen to have higher scores in developmental level of overhand throwing and higher scores for the Caltrac accelerometer, rapid-trunk movement, and motor skill related physical activity. Girls were seen to have higher scores in lower-intensity physical activities and physical inactivity. The study showed that the developmental level of the fundamental skills (Overhand-throwing and Jumping) are related to skill-specific physical activity outside of school in elementary children. We can conclude that boys at a younger age develop fundamental motor skills quicker than girls will. In other studies it has been seen that having a higher motor proficiency leads to kids being more active, and in most cases more athletic. This can lead to some issues in childhood development such as issues with weight, and increasing the public health epidemic of childhood obesity. Adolescence and adulthood Between the ages of 7 and 12 there is an increase in running speed and are able to skip. Jumping is also acquired better and there is an increase in throwing and kicking. They’re able to bat and dribble a ball. (Age) Gross motor skills usually continue improving during adolescence. The peak of physical performance is before 3 ko0, between 18 and 26. Even though athletes keep getting better than their predecessors—running faster, jumping higher, and lifting more weight—the age at which they reach their peak performance has remained virtually the same. After age 30, most functions begin to decline. Older adults move slower than younger adults. This can be moving from one place to another or continually moving. Exercising regularly and maintaining a healthy lifestyle can slow this process. Aging individuals who are active and biologically healthy perform motor skills at a higher level than their less active, less healthy aging counterparts. See also Apraxia Developmental coordination disorder Fine motor skill References Further reading External links About Down Syndrome Gross motor development in early & middle childhood Infancy Physical Development: Gross Motor Skills - A. Oswalt Walking Development In Visually Impaired Children - A. Humphrey Watch How You Hold That Crayon - New York Times Category:Pediatrics Category:Motor control Category:Motor skills
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Horwood PF, Karlsson EA, Horm SV, et al. Circulation and characterization of seasonal influenza viruses in Cambodia, 2012‐2015. Influenza Other Respi Viruses. 2019;13:465--476. 10.1111/irv.12647 1. BACKGROUND {#irv12647-sec-0006} ============= Influenza viruses belong to the *Orthomyxoviridae* family of enveloped, segmented negative‐stranded RNA viruses. Currently, four antigenically distinct influenza viruses are responsible for human seasonal influenza infections, including two subtypes of influenza A \[A(H1N1)pdm09 and A(H3N2)\] and two lineages of influenza B (B/Yamagata and B/Victoria). Influenza is responsible for a large proportion of human morbidity and mortality as a result of infections worldwide. Annual influenza infections are estimated to result in approximately 3 to 5 million cases of severe illness globally,[1](#irv12647-bib-0001){ref-type="ref"} and 290 000 to 650 000 deaths.[2](#irv12647-bib-0002){ref-type="ref"} Seasonal influenza epidemics occur every year in temperate regions during the winter months[3](#irv12647-bib-0003){ref-type="ref"}: November to March/April in the northern hemisphere and May to September in the southern hemisphere.[4](#irv12647-bib-0004){ref-type="ref"}, [5](#irv12647-bib-0005){ref-type="ref"} Influenza seasonality is more variable in tropical/subtropical regions where circulation can be observed year‐round, although activity is often more intense during rainy seasons.[6](#irv12647-bib-0006){ref-type="ref"} In addition, influenza activity is punctuated by occasional pandemics arising from the introduction of novel influenza A viruses into human circulation. These pandemics can significantly increase morbidity and mortality worldwide, with major economic impacts.[7](#irv12647-bib-0007){ref-type="ref"} We have previously described the circulation and seasonality of influenza viruses in Cambodia during six consecutive years (2006‐2011) following the establishment of the Cambodian National Influenza Centre (NIC) in 2006.[8](#irv12647-bib-0008){ref-type="ref"}, [9](#irv12647-bib-0009){ref-type="ref"}, [10](#irv12647-bib-0010){ref-type="ref"} These previous data demonstrated a peak in influenza circulation during the rainy season from June to November, which is consistent with influenza circulation in the southern hemisphere. However, year‐round circulation was also described, characteristic of influenza seasonality in tropical/subtropical regions, including some other Southeast Asian countries.[11](#irv12647-bib-0011){ref-type="ref"}, [12](#irv12647-bib-0012){ref-type="ref"} This current study furthers our understanding of influenza in Cambodia and describes the seasonal circulation, genetic and antigenic diversity, and antiviral drug susceptibility analyses of influenza viruses in Cambodia during four consecutive years (2012‐2015). 2. MATERIALS AND METHODS {#irv12647-sec-0007} ======================== 2.1. Ethical statement {#irv12647-sec-0008} ---------------------- The Cambodian ILI surveillance system is a public health activity managed by the Ministry of Health in Cambodia and has a standing authorization from the National Ethics Committee for Human Research. Samples and patient information were anonymized for the purpose of this surveillance. 2.2. Geographic background {#irv12647-sec-0009} -------------------------- Cambodia is a tropical climate country in Southeast Asia with more than 15.5 million people, situated in the southwestern part of the Indochina peninsula and sharing international borders with Thailand and Laos on the West and North, and Vietnam on the East and Southeast.[13](#irv12647-bib-0013){ref-type="ref"} The country is affected by the Asian monsoon and is mostly hot and humid with a mean temperature of 27ºC and mean relative humidity of 77.5%. Similar to other subtropical/tropical areas, Cambodia has two distinct seasons: the dry season, which generally runs from November to April; and the rainy season, which starts in May‐June and ends in October‐November. 2.3. ILI surveillance system in Cambodia {#irv12647-sec-0010} ---------------------------------------- The Cambodian National Influenza Center (NIC) was established in August 2006 at the Institute Pasteur in Cambodia (IPC). It is a joint collaboration between IPC, the Communicable Disease Control Department of the Ministry of Health (CDC/MoH), and the World Health Organization (WHO) office in Cambodia for documenting the dynamics of influenza disease and conducting virological characterization of circulating influenza strains. An outpatient sentinel surveillance system for influenza‐like illness (ILI) with a weekly reporting and sampling scheme was established. Six ILI sentinel surveillance sites were operated in the referral hospitals of Kampong Cham (Eastern Cambodia), Mondulkiri (Eastern Cambodia), Svay Rieng (Southeast Cambodia), and Kampot (Southwest Cambodia) Provinces; and in a children\'s hospital in Siem Reap (northwestern Cambodia) and in the national pediatric hospital in Phnom Penh (capital city of Cambodia) by the CDC/MoH in collaboration with the National Institute of Public Health (NIPH), with assistance from the US Centers for Disease Control and Prevention and WHO Cambodia. The Armed Forces Research Institute of Medical Sciences (AFRIMS) operated an additional five sentinel sites in northwestern Cambodia: Thmor Kol Health Center (Battambang Province), Ta Sahn Health Center (Battambang Province), Anlong Veng Referral Hospital (Oddar Meanchey Province), Banteay Meanchey Health Center (Banteay Meanchey Province), and Preah Punlea Health Centre (Pailin Province). The 11 hospital sites included in the Cambodian outpatient surveillance system for ILI are presented in Figure [1](#irv12647-fig-0001){ref-type="fig"}. ![Map of Cambodia showing the influenza‐like illness sentinel surveillance sites and supporting laboratories. ILI, influenza‐like illness; AFRIMS, Armed Forces Research Institute of Medical Sciences; NIPH, National Institute of Public Health; IPC, Institute Pasteur in Cambodia; NIC, National Influenza Centre](IRV-13-465-g001){#irv12647-fig-0001} The case definition for ILI was defined as previously described by WHO: sudden onset of fever (≥38ºC axillary temperature) and cough or sore throat in the absence of other diagnosis.[9](#irv12647-bib-0009){ref-type="ref"}, [14](#irv12647-bib-0014){ref-type="ref"} 2.4. Specimen collection {#irv12647-sec-0011} ------------------------ Between January 2012 and December 2015, specimens and surveillance data were collected from a subset of outpatients presenting with ILI at sentinel surveillance sites. During 2012, ILI samples were collected as described previously.[9](#irv12647-bib-0009){ref-type="ref"} Starting in 2013 (and continuing through 2015), primary testing was shifted to the NIPH and AFRIMS laboratories, with the NIC concentrating on reference center activities. As such, during 2013‐2015 all ILI samples were first screened by the laboratories at NIPH or AFRIMS and then influenza‐positive samples (plus \~30% negative samples for quality control testing) were forwarded to the NIC for confirmation and viral characterization. 2.5. Laboratory methods {#irv12647-sec-0012} ----------------------- At the NIC, viral RNA was extracted using the QIAamp Viral RNA Mini Kit (Qiagen, CA, USA) and amplified using real‐time RT‐PCR to detect influenza A and B viruses using standard protocols. Influenza A viruses were subsequently subtyped using subtype‐specific real‐time reverse transcriptase polymerase chain reaction (RT‐qPCR) assays targeting H1pdm, H1, H3, H5, H7, N1pdm, N1, and N2 genes.[8](#irv12647-bib-0008){ref-type="ref"}, [9](#irv12647-bib-0009){ref-type="ref"} All influenza primers were sourced from the International Reagent Resource (<https://www.internationalreagentresource.org/Home.aspx>). Influenza viruses were isolated at the IPC laboratory by inoculation of the specimens that tested positive by real‐time RT‐PCR onto Madin‐Darby canine kidney (MDCK) cells in an enhanced biosafety level 2 laboratory.[9](#irv12647-bib-0009){ref-type="ref"} The influenza isolates were characterized by hemagglutination inhibition assay (HAI) using reference antigens and anti‐sera provided by the WHO Collaborating Center (WHOCC) for Reference and Research on Influenza in Melbourne, Australia. A representative number of influenza isolates were sent each year to the WHOCC in Melbourne for confirmation and further analysis, including antiviral testing and partial or full genome sequencing of representative viruses. 2.6. Genome sequencing and phylogenetic analysis {#irv12647-sec-0013} ------------------------------------------------ Viral RNA extracted from MDCK supernatant was used to sequence the HA gene of all influenza isolates at the NIC laboratory using Sanger sequencing. At the WHOCC (Melbourne), a single‐reaction, multiplex RT‐PCR method that amplifies the HA, NA, and M genomic segments of seasonal influenza A and B viruses for next‐generation sequencing was used, as previously described.[15](#irv12647-bib-0015){ref-type="ref"} Nucleotide sequences from the coding regions of the HA genes of A(H3N2), A(H1N1)pdm09, and influenza B viruses were aligned using the Mafft multiple aligner V1.3.7 in the Geneious V10.0.9 software package ([www.geneious.com](http://www.geneious.com)). Sequences originating from Cambodia, surrounding countries, and representative reference sequences were downloaded from the EpiFlu™ Database ([www.gisaid.org](http://www.gisaid.org)). Maximum likelihood trees were estimated using PhyML 3.0[16](#irv12647-bib-0016){ref-type="ref"} with 1000 bootstrap replicates using the ATGC server (<http://www.atgc-montpellier.fr/phyml/execution>). The most appropriate nucleotide substitution method determined for each data set was the GTR + G model. The complete matrix gene was sequenced from representative influenza A viruses using previously described methods,[15](#irv12647-bib-0015){ref-type="ref"} to ascertain the presence of mutations (eg, Ser31Asn) associated with resistance to the adamantine class of inhibitors. 2.7. Nucleotide sequence accession numbers {#irv12647-sec-0014} ------------------------------------------ All Cambodian influenza A(H3N2), A(H1N1)pdm09, and influenza B viral sequences included in the analysis were submitted to the EpiFlu™ Database, and all of these sequences are available via the GISAID website (<https://www.gisaid.org/>). Table [S1](#irv12647-sup-0001){ref-type="supplementary-material"} provides detailed information about all of the Cambodian isolates and sequences analyzed in this study. 2.8. Antiviral susceptibility testing {#irv12647-sec-0015} ------------------------------------- All influenza isolates sent each year to the WHOCC in Melbourne were analyzed for neuraminidase (NA) inhibitor susceptibility testing using an enzyme inhibition assay utilizing the fluorescent substrate MUNANA as described previously.[17](#irv12647-bib-0017){ref-type="ref"} The concentration of drug required to inhibit 50% of the NA activity (IC50) was calculated using the non‐linear curve fitting function in the GraphPad Prism 4 package (GraphPad Software). The average IC~50~ (nM) (± standard deviation) of two independent determinations was calculated for each virus. Outliers of more than two standard deviations from the overall mean were retested twice.[18](#irv12647-bib-0018){ref-type="ref"} Antiviral susceptibility was classified according to the guidelines from the WHO working group on surveillance of influenza antiviral susceptibility.[18](#irv12647-bib-0018){ref-type="ref"} 2.9. Statistical analysis {#irv12647-sec-0016} ------------------------- The comparisons between percentages and two means were tested by chi‐squared (χ^2^) and Student\'s t test, respectively. A p value \< 0.05 was considered statistically significant. Proportions, means, and all statistical analyses were performed using STATA 9.0 (Statacorp). 3. RESULTS {#irv12647-sec-0017} ========== 3.1. Influenza activity in Cambodia {#irv12647-sec-0018} ----------------------------------- During 2012‐2015, 3,222 specimens were submitted to the Cambodian NIC and analyzed as part of the ILI surveillance system (Table [1](#irv12647-tbl-0001){ref-type="table"}). Influenza virus was detected in 1,238 samples during this period: 324 in 2012, 335 in 2013, 263 in 2014, and 316 in 2015. Influenza A viruses (n = 856, 69.1%) were detected more frequently than influenza B viruses (n = 382, 30.9%). A(H1N1)pdm09 and A(H3N2) viruses constituted 20.1% (n = 172) and 79.9% (n = 684) of influenza A virus subtypes detected, respectively. ###### The detection and isolation of influenza viruses associated with influenza‐like illness (ILI) in Cambodia during 2012‐2015   Samples received by NIC Influenza‐positive samples Successful influenza isolation[a](#irv12647-note-0001){ref-type="fn"}, [b](#irv12647-note-0002){ref-type="fn"} Isolates sent to WHO CC ------- --------------------------------------------- ---------------------------- ---------------------------------------------------------------------------------------------------------------- ------------------------- ------ ----- ----- ----- ---- ---- ---- 2012 1907[c](#irv12647-note-0003){ref-type="fn"} 26 218 80 324 6 88 50 0 37 1 2013 467 91 24 220 335 63 9 154 55 7 51 2014 404 36 212 15 263 33 174 11 11 30 3 2015 444 19 230 67 316 13 123 61 7 21 10 Total 3222 172 684 382 1238 115 194 276 73 95 65 Influenza viruses were isolated in Madin‐Darby canine kidney (MDCK) cells. Virus isolation was only attempted on samples with high viral load, as determined by RT‐qPCR CT values. During 2012 first‐line screening was conducted by the National Influenza Centre (NIC). John Wiley & Sons, Ltd Co‐circulation of A(H1N1)pdm09, A(H3N2), and influenza B viruses were detected across all four years, with A(H3N2) being the dominant subtype in 2012, 2014, and 2015; and influenza B the dominant virus in 2013. Both lineages of influenza B virus, B/Yamagata and B/Victoria, were detected across all four years, except in 2013 where only the B/Yamagata‐lineage was detected. From 2012 to 2015, influenza seasonality varied, with peak circulation occurring from September to December in 2012 and 2013; and from May to August in 2014 and 2015 (Figure [2](#irv12647-fig-0002){ref-type="fig"}). ![Number of specimens positive for influenza by subtype in Cambodia 2012‐2015 by week. Cambodian data accessed fromthe Global Initiative on Sharing All Influenza Data (GISAID---<https://www.gisaid.org/>)](IRV-13-465-g002){#irv12647-fig-0002} Of the samples tested, the average age of influenza patients was 8.8 years (range, 4 days to 77 years) and 55.2% were male. The age and gender distribution of each year and across the four testing years (2012‐2015) for influenza patients are presented in Table [S2](#irv12647-sup-0002){ref-type="supplementary-material"}. 3.2. Antigenic analysis {#irv12647-sec-0019} ----------------------- Generally, Cambodian seasonal influenza virus isolates matched the southern hemisphere trivalent inactivated influenza vaccine (TIIV) formulations during the relevant year they were released (Table [2](#irv12647-tbl-0002){ref-type="table"}). Antigenic analysis revealed that all of the A(H1N1)pdm09 isolates circulating in Cambodia during 2012‐2015 belonged to the A/California/7/2009(H1N1)‐like group. Mismatches occurred in 2012 when an A/Perth/16/2009(H3N2)‐like virus was included in both of the northern and southern hemisphere TIIVs, but A/Victoria/361/2011(H3N2)‐like viruses were the dominant circulating strains; also in 2012, a B/Brisbane/60/2008‐like virus was included in both of the northern and southern hemisphere TIIVs, but B/Wisconsin/1/2010‐like was the dominant strain; in 2014, the northern hemisphere formulation of TIIVs included an A/Victoria/361/2011(H3N2)‐like virus, but the dominant strain in Cambodia was A/Texas/50/2012(H3N2)‐like (which matched the southern hemisphere formulation); in 2015, an A/Texas/50/2012(H3N2)‐like virus was included in the northern hemisphere formulation of TIIVs, but A/Switzerland/9715293/2013(H3N2)‐like viruses were the dominant strains (which matched the southern hemisphere formulation); also in 2015, a B/Massachusetts/2/2012‐like was included in the northern hemisphere formulations of TIIVs, but the dominant circulating viruses were B/Phuket/3073/2013‐like (which matched the southern hemisphere formulation). ###### The seasonal influenza strains circulating in Cambodia (2012‐2015) compared to the strains included in the WHO‐recommended vaccine formulations for trivalent influenza vaccines; viruses in bold indicate where the dominant Cambodian strain matched the vaccine strain --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Year Virus Trivalent inactivated influenza vaccine strains Cambodian circulating strains[b](#irv12647-note-0005){ref-type="fn"}\ (proportion of Cambodian isolates) ------------- --------------------------------- ------------------------------------------------- ----------------------------------------------------------------------- ------------------------------------- 2012 A/H1N1pdm09 **A/California/7/2009‐like** **A/California/7/2009‐like** **A/California/7/2009‐like (100%)** A/H3N2 A/Perth/16/2009‐like A/Perth/16/2009‐like A/Victoria/361/2011‐like (91%) A/Perth/16/2009‐like (9%) Influenza B B/Brisbane/60/2008‐like B/Brisbane/60/2008‐like B/Wisconsin/1/2010‐like (70%)\ B/Brisbane/60/2008‐like (30%) 2013 A/H1N1pdm09 **A/California/7/2009‐like** **A/California/7/2009‐like** **A/California/7/2009‐like (100%)** A/H3N2 **A/Victoria/361/2011‐like** **A/Victoria/361/2011‐like** **A/Victoria/361/2011‐like (100%)** Influenza B **B/Wisconsin/1/2010‐like** **B/Wisconsin/1/2010‐like** **B/Wisconsin/1/2010‐like (52%)**\ B/Massachusetts/2/2012‐like (43%)\ B/Brisbane/60/2008‐like (5%) 2014 A/H1N1pdm09 **A/California/7/2009‐like** **A/California/7/2009‐like** **A/California/7/2009‐like (100%)** A/H3N2 A/Victoria/361/2011‐like **A/Texas/50/2012‐like** **A/Texas/50/2012‐like (69%)**\ A/Victoria/361/2011‐like (30%)\ A/Switzerland/9715293/2013‐like (1%) Influenza B **B/Massachusetts/2/2012‐like** **B/Massachusetts/2/2012‐like** **B/Massachusetts/2/2012‐like (100%)** 2015 A/H1N1pdm09 **A/California/7/2009‐like** **A/California/7/2009‐like** **A/California/7/2009‐like (100%)** A/H3N2 A/Texas/50/2012‐like **A/Switzerland/9715293/2013‐like** **A/Switzerland/9715293/2013‐like** (76%)\ A/Hong Kong/4801/2014‐like (24%) Influenza B B/Massachusetts/2/2012‐like **B/Phuket/3073/2013‐like** **B/Phuket/3073/2013‐like (96%)**\ B/Brisbane/60/2008‐like (4%) --------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Northern Hemisphere vaccination periods occur mid‐year that is 2012 (2011/2012); 2013 (2012/2013); 2014 (2013/2014); 2015 (2014/2015). B/Brisbane/60/2008‐like viruses belong to the B/Victoria /7/87 lineage. B/Wisconsin/1/2010‐like viruses, B/Massachusetts/2/2012‐like viruses, and B/Phuket/3073/2013‐like viruses belong to the B/Yamagata/16/88 lineage. John Wiley & Sons, Ltd 3.3. Neuraminidase inhibitor susceptibility analysis {#irv12647-sec-0020} ---------------------------------------------------- A total of 148 A(H3N2), 73 A(H1N1)pdm09, and 83 influenza B viruses were tested for susceptibility to the neuraminidase inhibitors oseltamivir and zanamivir. The analysis demonstrated that all of the tested isolates were sensitive to both drugs (Table [S4](#irv12647-sup-0004){ref-type="supplementary-material"}). Full NA gene sequences were also generated for 68 A(H3N2), 25 A(H1N1)pdm09, and 48 influenza B viruses and confirmed that none contained mutations associated with NA inhibitor resistance (Table [S3](#irv12647-sup-0003){ref-type="supplementary-material"}). 3.4. Sequence analysis of the matrix gene for mutations associated with amantadine resistance {#irv12647-sec-0021} --------------------------------------------------------------------------------------------- Sequencing of the matrix gene was completed for representative A(H1N1)pdm09 (n = 27) and A(H3N2) (n = 66) viruses from 2012 to 2015. Sequence analysis showed that all of the Cambodian isolates contained an amino acid change from serine to asparagine at position 31 (Ser31Asn) in the M2 protein, which is associated with resistance to the adamantine class of inhibitors (Tables [S4](#irv12647-sup-0004){ref-type="supplementary-material"} and [S5](#irv12647-sup-0005){ref-type="supplementary-material"}). 3.5. Phylogenetic analysis of A(H1N1)PDm09 Isolates {#irv12647-sec-0022} --------------------------------------------------- Phylogenetic analysis of the HA gene sequences was carried out for 70 representative Cambodian A(H1N1)pdm09 isolates from 2012 to 2015 (Figure [3](#irv12647-fig-0003){ref-type="fig"}; GISAID accession numbers are listed in Table [S1](#irv12647-sup-0001){ref-type="supplementary-material"}). The HA sequences for clade reference strains (A/Darwin/56/2013, A/Michigan/45/2015, and A/South Australia/22/2015) and the vaccine strain (A/California/07/2009) were also included in the phylogenetic analysis. All Cambodian A(H1N1)pdm09 isolates clustered with clade 6B.1 viruses, except one isolate (A/Cambodia/W1101376/2012) which was isolated in 2012 and grouped with the reference strain A/Darwin/56/2013 in clade 6B.2. Interestingly, three Cambodian A(H1N1)pdm09 isolates from 2015 were grouped with the reference strain A/Michigan/45/2015 from clade 6B.1. All specific amino acid changes corresponding to each group of viruses are indicated in Figure [3](#irv12647-fig-0003){ref-type="fig"}. ![Phylogenetic analysis of the HA genes (sequences of 1650 nucleotides (nt49--1698)) of influenza A(H1N1)pdm09 virus isolates collected in Cambodia from 2012 to 2015. The phylogenetic analysis was conducted as a maximum likelihood phylogenetic tree of influenza using the GTR + G nucleotide substitution model with 1000 bootstrap replicates (values given on the branches) and rooted to A/California/07/2009. Major amino acid changes are shown in block letter at the appropriate nodes. Year of isolation is indicated by color: 2012---blue, 2013---green, 2014---yellow, 2015---purple. Vaccine strains are indicated in bold red. Other reference viruses are indicated in black. Scale bar indicates the number of nucleotide substitution per site](IRV-13-465-g003){#irv12647-fig-0003} 3.6. Phylogenetic analysis of A(H3N2) isolates {#irv12647-sec-0023} ---------------------------------------------- Phylogenetic analysis of the HA gene sequences was carried out for 108 representative A(H3N2) isolates from 2012 to 2015 in Cambodia. Additional reference sequences corresponding to vaccine candidate strains and A(H3N2) clade reference strains were included in the analysis. HA sequences of the A(H3N2) viruses isolated during the four consecutive seasons fell into four distinct clusters corresponding with each new influenza season (Figure [4](#irv12647-fig-0004){ref-type="fig"}; GISAID accession numbers are listed in Table [S1](#irv12647-sup-0001){ref-type="supplementary-material"}): clade 3C.1 contained the majority of isolates from 2012; clade 3C.3b contained two viruses isolated in 2013 (A/Cambodia/X0828305/2013 and A/Cambodia/X0906313/2013) and some isolates from 2014; clade 3C.3a contained most of the isolates obtained in 2014; and clade 3C.2a contained two isolates from 2012 (A/Cambodia/W1023355/2012 and A/Cambodia/W0718409/2012), some isolates from 2013, two isolates from 2014 (A/Cambodia/Y1204313/2014 and A/Cambodia/Y1218307/2014), and all isolates obtained in 2015. The viruses in clade 3C.1 were closely related to the vaccine strain A/Texas/50/2012. The two isolates from 2013 and some isolates from 2014 that belonged to clade 3C.3b contained four more mutations compared to clade 3C.1. The Cambodian A(H3N2) viruses isolated in 2014 diverged into two clades. Some of the 2014 viruses belonged to clade 3C.3b with the reference A/Newcastle/22/2014 strain; however, the majority of isolates from 2014 were grouped with the vaccine strain A/Switzerland/9715293/2013, clade 3C.3a. The Cambodian A(H3N2) isolates belonging to clade 3C.2a were represented by the reference strain A/New Caledonia/104/2014 and the vaccine strain A/Hong Kong/4801/2014. All specific amino acid changes corresponding to each clade are indicated in Figure [4](#irv12647-fig-0004){ref-type="fig"}. ![Phylogenetic analysis of the HA genes (sequences of 1653 nucleotides (nt49--1701) of influenza A(H3N2) virus isolates collected in Cambodia from 2012 to 2015. The phylogenetic analysis was conducted as a maximum likelihood phylogenetic tree of influenza using the GTR + G nucleotide substitution model with 1000 bootstrap replicates (values given on the branches) and rooted to A/Texas/50/2012. Major amino acid changes are shown in block letters at the appropriate nodes. Year of isolation is indicted by color: 2012---blue, 2013---green, 2014---yellow, 2015---purple. Vaccine strains are indicated in bold red. Other reference viruses are indicated in black. Scale bar indicates the number of nucleotide substitution per site](IRV-13-465-g004){#irv12647-fig-0004} 3.7. Phylogenetic analysis of influenza B isolates {#irv12647-sec-0024} -------------------------------------------------- Phylogenetic analysis of the HA gene sequences was carried out for 56 representative Cambodian influenza B isolates from 2012 to 2015 (Figure [5](#irv12647-fig-0005){ref-type="fig"}; GISAID accession numbers and listed in Table [S1](#irv12647-sup-0001){ref-type="supplementary-material"}). The Cambodian influenza B viruses were compared to the reference strains for B/Yamagata (B/Wisconsin/01/2010, B/Massachusetts/02/2012, and B/Phuket/3073/2013), and B/Victoria (B/Brisbane/60/2008) lineages. During this period, the majority of influenza B viruses circulating in Cambodia belonged to the B/Yamagata‐lineage. However, Cambodian influenza B isolates belonging to the B/Victoria‐lineage were also detected in 2012, 2013, and 2015. All of the Cambodian B/Victoria‐lineage strains clustered with B/Brisbane/46/2015 (clade V1.A). Two subgroups emerged within the Cambodian B/Yamagata‐lineage. One subgroup (B/Yamagata‐lineage, clade Y2), with most of the Cambodian isolates collected in 2013 and three isolates from 2014, was closely related to the vaccine strain B/Massachusetts/02/2012. The other subgroup of Cambodian influenza B/Yamagata‐lineage grouped with the vaccine strain B/Phuket/3073/2013 (B/Yamagata‐lineage, clade Y3), which included some of the isolates collected in 2014 and almost all isolates from 2015. All specific amino acid changes corresponding to each group of viruses are indicated in Figure [5](#irv12647-fig-0005){ref-type="fig"}. ![Phylogenetic analysis of the HA genes (sequences of 1710 nucleotides (nt 46--1755)) of influenza B virus isolates collected in Cambodia from 2012 to 2015. The phylogenetic analysis was conducted as a maximum likelihood phylogenetic tree of influenza using the GTR + G nucleotide substitution model with 1000 bootstrap replicates (values given on the branches) and rooted to B/Brisbane/60/2008. Major amino acid changes are shown in block letters at the appropriate nodes. Year of isolation is indicted by color: 2012---blue, 2013---green, 2014---yellow, 2015---purple. Vaccine strains are indicated in bold red. Other reference viruses are indicated in black, and the two major lineages B/Victoria‐like and B/Yamagata‐like are shown on the same figure. Scale bar indicates the number of nucleotide substitution per site](IRV-13-465-g005){#irv12647-fig-0005} 4. DISCUSSION {#irv12647-sec-0025} ============= During the surveillance period (2012‐2015), influenza circulation was dominated by A(H3N2), comprising 55% of the viruses detected, followed by influenza B (31%; predominantly B/Yamagata‐lineage) and A(H1N1)pdm09 (14%). These figures closely reflect influenza virus circulation during this period in the WHO Western Pacific Region, where A(H3N2) (51%), influenza B (32%), and A(H1N1)pdm09 (17%) were detected in similar proportions.[19](#irv12647-bib-0019){ref-type="ref"} Previous surveillance of influenza circulation in Cambodia from 2006‐2011[8](#irv12647-bib-0008){ref-type="ref"}, [9](#irv12647-bib-0009){ref-type="ref"}, [10](#irv12647-bib-0010){ref-type="ref"} revealed a consistent peak during the Cambodian rainy season from June to November, which broadly coincided with peak influenza circulation in the southern hemisphere. However, year‐round co‐circulation of multiple influenza subtypes reflected a similar pattern observed in many tropical countries. Hence, the Cambodian pattern of influenza transmission was postulated as intermediate between the temperate southern hemisphere and tropical countries.[9](#irv12647-bib-0009){ref-type="ref"} These general patterns were repeated in 2012‐2015. However, an earlier peak in influenza circulation was observed in 2014 (April‐August) and 2015 (June‐September), which coincided with the circulation of the clade 3C.2a and 3C.3a A(H3N2) viruses, the dominant viruses in these seasons, respectively. An unusual, earlier peak in seasonal influenza circulation, associated with A(H3N2) clade 3C.2a, was also observed in South Korea during 2016‐2017.[20](#irv12647-bib-0020){ref-type="ref"} There was also some evidence of bimodal circulation during 2014‐2015, particularly in 2015 when a second peak in influenza circulation was noted during October‐December, linked with an increase in influenza B cases. In all years included in the study, except 2014, influenza B viruses were primarily detected at the end of the influenza season, as influenza A cases were starting to wane. This pattern of influenza B circulation has previously been noted in Cambodia and other countries globally.[9](#irv12647-bib-0009){ref-type="ref"}, [21](#irv12647-bib-0021){ref-type="ref"} Seasonal influenza vaccination is not widespread in Cambodia, but considering the co‐circulation of both influenza B lineages in most years since surveillance began in 2006,[8](#irv12647-bib-0008){ref-type="ref"}, [9](#irv12647-bib-0009){ref-type="ref"} and the frequent mismatch between strains included in the TIIVs and the most dominant circulating influenza B lineage, the introduction of the quadrivalent seasonal influenza vaccine might be worthwhile, especially in young children, as this covers both lineages of influenza B virus and both subtypes of seasonal influenza A viruses.[22](#irv12647-bib-0022){ref-type="ref"} Antigenic characterization of Cambodian influenza isolates from 2012 to 2015 largely corresponded with the southern and northern hemisphere vaccine formulations. Vaccination for seasonal influenza is still rare in Cambodia, with vaccines generally only available through private clinics.[9](#irv12647-bib-0009){ref-type="ref"}, [23](#irv12647-bib-0023){ref-type="ref"} Future policies for the introduction of seasonal vaccination in Cambodia will be aided by the distinct seasonality of influenza circulation, which is unusual for a tropical country, and should be aligned with a vaccination program mirroring the WHO southern hemisphere vaccination formulation timetable with vaccinations ideally taking place in March‐April. Recent introduction of seasonal alert thresholds in Cambodia[24](#irv12647-bib-0024){ref-type="ref"} using the "WHO method"[25](#irv12647-bib-0025){ref-type="ref"} will also help to refine the ideal vaccination timing. There was no detection of seasonal influenza isolates with resistance to the commonly used antivirals oseltamivir and zanamivir in Cambodia during 2012‐2015. These antivirals are generally not used in Cambodia during seasonal influenza infections, so resistance is unlikely to be affected by domestic antiviral use. Following the widespread reporting of adamantane resistance in A(H3N2) strains from 2005 and the emergence of the A(H1N1)pdm09 virus (which was already adamantane‐resistant), this antiviral is no longer recommended for use.[26](#irv12647-bib-0026){ref-type="ref"}, [27](#irv12647-bib-0027){ref-type="ref"} Sequence analysis of the matrix gene from representative Cambodian isolates suggested that resistance to adamantanes is common, as all isolates obtained during this period contained the Ser31Asn mutation in the M2 protein. This situation is still reflected currently with most isolates globally being resistant,[27](#irv12647-bib-0027){ref-type="ref"} despite the almost complete cessation in the use of adamantanes. Samples from patients with ILI were collected through two different surveillance systems (managed by the NIPH and AFRIMS laboratories), leading to limitations in the analyses presented in this paper. However, any possible biases in the representativeness of viruses are likely countered by the large number of samples collected throughout the surveillance period and the large number of sentinel sites, covering most of the country. Individual patient data are compiled at the national level by the Cambodian Ministry of Health and was not analyzed by the Cambodian NIC. As such, epidemiological information such as disease severity and infection rates could not be included in these analyses. The large number of influenza‐positive samples (n = 1,238) received by the NIC during this period meant that only representative isolates could be included for genetic and antigenic characterization, meaning that some isolates with interesting characteristics could have been missed. Despite these limitations, we believe that the results are representative of the circulation and genetic/antigenic/antiviral characteristics of seasonal influenza strains in Cambodia during 2012‐2015. Our data concur with the findings from previous studies describing the seasonal circulation of influenza viruses in Cambodia with year‐round co‐circulation of multiple influenza subtypes.[8](#irv12647-bib-0008){ref-type="ref"}, [9](#irv12647-bib-0009){ref-type="ref"}, [10](#irv12647-bib-0010){ref-type="ref"}, [24](#irv12647-bib-0024){ref-type="ref"} Influenza viruses detected in Cambodia continued to be susceptible to oseltamivir and zanamivir, but resistance to adamantanes was still universal in influenza A viruses. Antigenically, there was considerable drift in the A(H3N2) viruses and some in the influenza B viruses (B/Yamagata‐lineage viruses more than B/Victoria‐lineage viruses) during 2012‐2015, but little change in A(H1N1)pdm09 viruses. Seasonal influenza surveillance has been strengthened in Cambodia since being established in 2006 and continues to contribute to our knowledge of the regional and global circulation of seasonal influenza strains. 5. DISCLAIMER {#irv12647-sec-0026} ============= Material has been reviewed by the Walter Reed Army Institute of Research. There is no objection to its presentation and/or publication. The opinions or assertions contained herein are the private views of the author and are not to be construed as official, or as reflecting true views of the Department of the Army or the Department of Defense. The investigators have adhered to the policies for protection of human subjects as prescribed in AR 70--25. Supporting information ====================== ######   ###### Click here for additional data file. ######   ###### Click here for additional data file. ######   ###### Click here for additional data file. ######   ###### Click here for additional data file. ######   ###### Click here for additional data file. The study was funded by the World Health Organization office in Cambodia. The authors gratefully acknowledge the staff from the participating hospitals, laboratories, and Cambodian Ministry of Health for contributing to the Cambodian ILI sentinel surveillance System. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention. Funding for samples collected by AFRIMS was provided by the Armed Forces Health Surveillance Center (AFHSC).
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Testicular trauma Testicular trauma is an injury to one or both testicles. Types of injuries include blunt, penetrating and degloving. Because the testes are located within the scrotum, which hangs outside of the body, they do not have the protection of muscles and bones. This makes it easier for the testes to be struck, hit, kicked or crushed, which occurs most often during contact sports. Testicles can be protected by wearing athletic cups during sports. Trauma to the testes can cause severe pain, bruising, swelling, and/or in severe cases even infertility. In most cases, the testes—which are made of a spongy material—can absorb some impact without serious damage. A rare type of testicular trauma, called testicular rupture, occurs when a testicle receives a direct blow or is squeezed against the hard bones of the pelvis. This injury can cause blood to leak into the scrotum and possibly even infertility and other complications. In severe cases, surgery to repair the rupture—and thus save the testicle—may be necessary. In at least one case, testicular trauma was reported as the cause of a patient developing Systemic inflammatory response syndrome (SIRS) despite otherwise minor trauma. See also Ball-busting Groin attack Testicular torsion References External links Category:Testicle disorders Category:Men's health
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Electrodynamics/Ampere's Law In physics, Ampère's Circuital law, discovered by André-Marie Ampère, relates the circulating magnetic field in a closed loop to the electric current passing through the loop. It is the magnetic equivalent of Gauss's Law. James Clerk Maxwell conceived of displacement current as a polarization current in the dielectric vortex sea which he used to model the magnetic field hydrodynamically and mechanically. He added this displacement current to Ampère's Circuital law at equation (112) in his 1861 paper On Physical Lines of Force. The generalized law, as corrected by Maxwell, takes the following integral form: [Ampere-Maxwell Law] where in linear media is the displacement flux density (in coulombs per square meter). This Ampère-Maxwell law can also be stated in differential form: where the second term arises from the displacement current. With the addition of the displacement current, Maxwell was able to postulate (correctly) that light was a form of electromagnetic wave. See Electromagnetic wave equation for a discussion on this important discovery. We will discuss all of Maxwell's laws in a later chapter. The Equivalent to Gauss's Law for Electricity is Ampère's Law in Magnetism. It's a bit more complicated and you should know Gauss's before getting a grip on this one. Imagine a wire with current flowing through it, the right hand screw rule says that there will be a magnetic field curling around the way your fingers do with your thumb pointing the direction of conventional current. You can predict that the magnetic field will be curling around proportionally to the current flowing. Ampère's Law will tell you how.
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The history of cardiopulmonary resuscitation. The development of modern cardiopulmonary resuscitation (CPR) is an exciting and surprising history to modern health professionals who rarely are aware of how new CPR really is. Artificial respiration began in the 16th century with Vesalius's work on living animals; progressed with the rise and fall of mouth-to-mouth, manual, and positive pressure ventilation methods of the 18th and 19th centuries; and culminated in 1958 with demonstration of the superiority of the mouth-to-mouth technique. Cardiac massage began in 1874, with the open chest method gaining ascendancy until the 1960 demonstration of the equality and greater ease of closed chest cardiac massage. Electrical defibrillation may have begun in 1775, but was not proven successful in animals internally until 1899. The technique was applied to man internally in 1947 and externally in 1956. The simultaneous use of all these modern CPR methods dates back only 20 years.
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Q: How should i guide a program to perform correct things? I want to make a small model of A.I. which can learn itself. I am inspired by 1000+ monkey theorem which states that if 1000+ monkey bangs a keyboard for enough long, then they will eventually produce a Shakespeare's play. So, if you give a banana to one monkey when he produce a correct word, then he would eventually learn to do correct things. I think it is related to neural network. So, practically i want to start with basic alphabets and digits and then my program would permutate and combine those to form words. Now, if the words they form matches with those in English Dictionary, i want to reward the program. However i couldn't think of any possible approach to this. How could this be implemented? A: The "Infinite Monkey Theorem" doesn't say that monkeys will learn. On the contrary: it says that if monkeys keep typing random stuff long enough (i.e. not using any sort of learning), the works of Shakespeare will eventually come out purely by chance. It is the Law of Truly Large Numbers. So you're right: you need to build feedback into the system. The program should change its behavior based on your feedback. This is known as reinforcement learning and it is used a lot in AI. An overarching term for this, I believe, is machine learning.
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Ignoring occasional flare-ups such as supernovas, the farthest star we can reliably see with the naked eye is the obscure V762 Cassiopeiae, which is just visible under dark skies and is around 16,300 light years away. The most distant well-known star, meanwhile, is Deneb, the brightest star in the constellation of Cygnus, the Swan. It lies a still impressive 2,600 light years away and is the 19th brightest star in the sky, suggesting it is around 200,000 times more luminous than the Sun.
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Q: Knowing a geography coordinate nearby I am using geographic coordinates (latitude, longitude). I have the coordinates of each corner of a wall. I would like to know the coordinates of a point 10cm to the right of the lower left. I am not sure if it is possible. Thanks. A: Simple method Since latitude and longitude are a system of coordinates on a non-Euclidian surface (spherical 2-space), they are pretty awkward to work with directly. I'd suggest the following. Convert your two coordinates to 3D Cartesian vectors: z = R * sin(latitude); Rcoslat = R * cos(latitude); x = Rcoslat * cos(longitude); y = Rcoslat * sin(longitude); with R = 6378 km the (mean) radius of the Earth. Note that most trig functions in most computer languages take their argument in radians, so you'll have to multiply any degrees you have by pi/180 before taking their sin() or cos(). Doing this for both coordinates of a side of the wall gives you two vectors v1 = (x1 y1 z1) v2 = (x2 y2 z2) The difference between these vectors will give you the proper direction to go in: v3 = v1-v2 (if v1 is your leftmost coordinate) v3 = v2-v1 (if v2 is your leftmost coordinate) The length of v3 is the width of your wall. Extend it by 10cm to get a new vector: L = sqrt( v3x*v3x + v3y*v3y + v3z*v3z ) (width of the wall) v4 = v3/L * (L+10cm) = v3 * (1 + 10cm/L) Note that you'll have to do some unit juggling there, since if you take R in kilometers, L will be in kilometers, too. Now that you have the new vector, you can convert it back to latitude/longitude: hypotxy = hypot( v4x, v4y) latitude = atan2( v4z, hypotxy ) longitude = atan2( v4y, v4x ) Where atan2 is the four-quadrant arctangent, and hypot(a,b) is just a fairly standard way to compute sqrt(a*a+b*b) with a greatly reduced risk of numerical over/underflow. Note again that the output of atan2 in most computer languages will be in radians, so if you want your latitude/longitude in degrees, you'll have to multiply the outcome by 180/pi. Any more accurate method The method above makes a few errors due to some simplifications that are hardly noticeable on small scales (like your ordinary everyday wall). But of your wall is actually the Great Wall of China, then you'll find that these errors become pretty unacceptable. The errors made are due to these assumptions: Latitude and longitude are coordinates on a sphere. Usually, they're not. If they come from a GPS receiver of some quality, they describe coordinates on the reference ellipsoid of the Earth. The conversion between these coordinates and a Cartesian vector is slightly more involved. The difference vector v3 is just that, a vector. A vector is a straight line segment, while the actual line connecting the points v1 and v2 is slightly curved (because the Earth is not flat). Extending v3 to find v4 will therefore introduce an error. You'll actually have to extend the curved line. Again, this can be done simply (by assuming the Earth is a sphere again, and using cross and dot products), or more accurately (by extending the line on the Earth's reference ellipsoid). These corrections are pretty specific and can get very long and very ugly, so I'll leave it at this. I think the "simple method" above suffices for your need anyway. Nevertheless, if you ever need to do it with more accuracy: If you're smart, you'll use some existing Geo software library for it. If you're smarter, you'll look up all the formulas and relevant information and make the implementation yourself, discover that your implementation has errors and side effects, correct them and learn from this again :)
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Q: Working of the compiler directive in C++ The #define compiler directive seems rather strange to me. I have read that no memory is allocated to it . #include <iostream> #define test 50 int main() { cout<<test; return 0; } The above function displays 50 even though no memory is allocated to the compiler directive #define How does compiler know that 50 is stored in it (test) without having any memory. A: Macros are not the same thing as variables. Your compiler will translate the program #include <iostream> #define test 50 int main() { cout << test; return 0; } to #include <iostream> int main() { cout << 50; return 0; } by replacing the name test by its value given at your #define statement. You might want to take a look at some tutorials you can find on the internet e.g.: #define getmax(a,b) ((a)>(b)?(a):(b)) This would replace any occurrence of getmax followed by two arguments by the replacement expression, but also replacing each argument by its identifier, exactly as you would expect if it was a function: // function macro #include <iostream> using namespace std; #define getmax(a,b) ((a)>(b)?(a):(b)) int main() { int x=5, y; y= getmax(x,2); cout << y << endl; cout << getmax(7,x) << endl; return 0; } A: Effectively, test is going to be replaced by 50 whereever it's encountered in the code prior to compilation. Because the replacement's not done at runtime there's no overhead.
3.25
3
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Published: July 17, 2020 Introduction {#sec1} ============ The coronavirus disease 2019 (COVID-19) pandemic is a tremendous threat globally. As of July 3, 2020, 216 countries have reported COVID-19 cases, with more than 10 million confirmed cases and approximately 518,000 deaths (<https://www.who.int/emergencies/diseases/novel-coronavirus-2019/situation-reports/>). The causative agent of COVID-19, SARS-CoV-2 causes a lower respiratory tract infection that can progress to severe acute respiratory syndrome and even multiple organ failure ([@bib23]; [@bib44]). SARS-CoV-2 is a single-stranded positive-strand RNA virus whose genome encodes four structural proteins: spike (S), small protein (E), matrix (M), and nucleocapsid (N) ([@bib3]). The S protein is a type I fusion protein that forms trimers on the surface of the virion. It is composed of two subunits, with S1 responsible for receptor binding and S2 for membrane fusion ([@bib36]; [@bib41]). The SARS-CoV-2 utilizes angiotensin-converting enzyme 2 (ACE2) as the receptor for entry into target cells ([@bib20]). Therefore, the S protein determines the infectivity of the virus and its transmissibility in the host ([@bib14]). As this protein is the major antigen inducing protective immune responses ([@bib8]; [@bib11]; [@bib21]; [@bib36]), all vaccines under development are directed against it. Clearly, it is pivotal to closely monitor antigenic evolution of the spike in the circulating viruses. As it is a heavily glycosylated protein, investigation of the effects of the site-specific glycans on infectivity and immune escape is also of unquestionable importance. RNA viruses are known to have higher mutation rates than DNA viruses ([@bib9]; [@bib19]). Amino acid changes in the surface protein can significantly alter viral function and/or interactions with neutralizing antibodies. For example, A226V of Chikungunya virus E1 protein facilitated its adaptability in the vector *Aedesalbopictus*, resulting in an increased transmissibility ([@bib31]). Similarly, A82V of Ebola virus GP protein led to increased viral infectivity and mortality ([@bib6]; [@bib32]). Moreover, the highly pathogenic avian influenza H5N1 with 4 amino acid changes demonstrated enhanced transmission ([@bib12]), whereas in H7N9, the combined amino acid change A143V/R148K of hemagglutinin decreased the sensitivity of the virus to neutralizing antibodies by more than 10 times ([@bib26]; [@bib27]). Although SARS-CoV-2 was only discovered in humans recently, mutations in the gene encoding Spike (S) protein are being continuously reported ([@bib4]; [@bib17]; [@bib28]; [@bib29]; [@bib34]). As of May 6, 2020, 329 naturally occurring variants in S protein have been reported in public domain. Notably, there were only 13 amino acid sites with a rate of more than 0.1%. Preliminary study suggested that the increased fatality rate may be associated with the most dominant variant D614G. Presumably, this change may have induced a conformational change in the S protein, thereby resulting in the increased infectivity ([@bib1]). However, it remains largely unclear as to whether these reported variants could influence viral infectivity, transmissibility, or reactivity with neutralizing antibodies. It is also well documented that mutations affecting glycosylation of viral proteins could also profoundly affect viral life cycle and its interaction with the host. For example, N-glycosylation at specific sites of the HIV-1 Env protein is critical for Env expression and assembly ([@bib10]; [@bib16]; [@bib37]). Deletion of certain glycosylation sites could decrease the binding of Env protein to the CD4 receptor, abolishing the infectivity of the resulting viral particles ([@bib10]). Moreover, glycosylation site mutations are also known to render the virus resistant to neutralization by the antibodies ([@bib37]; [@bib38]), whereas deletion of certain glycosylation sites in the H5N1 HA protein has been found to affect HA cleavage, replication, stability, and antigenicity ([@bib45]). It is of note that although the S protein of SARS-CoV-2 is much more heavily glycosylated, with 22 potential N-glycosylation sites ([@bib18]; [@bib35]), how these glycosylation sites could affect viral infectivity and antibody-mediated neutralization remains unknown. In this study, we investigated the biological significance of natural variants with amino acid change(s) as well as mutants at the putative N-linked glycosylation sites in the SARS-CoV-2 S protein. To achieve these, we generated 106 S mutants reported in the public domain or mutants at putative N-linked glycosylation sites and analyzed their infectivity and reactivity to neutralizing antibodies using the high-throughput pseudotyped virus system ([@bib25]). We report that some natural variants and N-linked glycan deleted mutants have evolved to possess remarkable alterations in their infectivity and antigenicity. Results {#sec2} ======= Construction of Pseudotyped Viruses with Natural Variants and Deletions of the Glycosylation Sites {#sec2.1} -------------------------------------------------------------------------------------------------- For ease of description in this communication, variants are referred to as those that occurred naturally (reported in GISAID) and mutants (investigational or experimental mutants) for those we introduced experimentally. For the analyses of variants, we first retrieved all S sequences reported in GISAID database up to May 6, 2020. Following removal of incomplete, redundant, and ambiguous sequences, a total of 13,406 sequences of the S protein were selected for alignment analyses. Using Wuhan-1 strain (GenBank: [MN_908947](ncbi-n:MN_908947){#interref55}) as a template, we have selected three groups of variants and mutants to construct the pseudotyped viruses. As shown in [Figure 1](#fig1){ref-type="fig"} , group A represents all high-frequency variants and combined variants with D614G across the entire S gene (29 strains) excluding receptor-binding domain (RBD) region. Group B includes variants in RBD (51 strains). Although the eight single mutations (i.e., Q239K, V341I, A435S, K458R, I472V, H519P, A831V, and S943T) in both groups A and B do not exist by themselves, they were found to occur in combination with D614G. Therefore, the pseudotyped viruses for the eight single mutants were also constructed to compare with the double mutants with D614G. Group C is comprised of 26 mutants at the putative glycosylation sites (22 sites). This group includes both variants (N74K, N149H, and T719A) and investigational mutants that we made for the analyses of the effects of glycosylation. Specifically, all 22 sites (N to Q) were made in the lab to generate 22 individual mutants; we also made a combination by deleting the two glycosylation sites in RBD.Figure 1Illustration of Amino Acid Changes Selected for This Study(A) Variants and combined variants with D614G across the entire S gene excluding the RBD region.(B) Variants in RBD.(C) Mutants at the putative glycosylation sites (22 sites). This group include mutations we introduced at all 22 putative glycosylation sites (N to Q), a combination of two glycosylation site mutations in RBD, and three naturally occurring variants, N74K, N149H, and T719A, with ablated glycosylation sites.High-frequency amino acid change sites (frequency \> 0.1%) are highlighted in red. See also [Table S1](#mmc1){ref-type="supplementary-material"}. In total, we have generated 106 pseudotyped viruses (i.e., 80 variants and 26 glycosylation mutants) ([Figure 1](#fig1){ref-type="fig"}). These viruses were prepared as described previously ([@bib25]; see [STAR Methods](#sec4){ref-type="sec"}). Significantly Altered Infectivity of Variants and Deletions of the Glycosylation Site Mutants {#sec2.2} --------------------------------------------------------------------------------------------- To determine the infectivity of these variants and mutants, we first infected 26 cell lines with pseudotyped viruses with either SARS-CoV-2 S protein or VSV G protein (see [STAR Methods](#sec4){ref-type="sec"}). As expected, the two types of pseudotyped viruses are different in the infection efficiency in the 26 cell lines ([Figure 2](#fig2){ref-type="fig"} ). Although almost all cell lines were generally susceptible to infection by VSV G pseudotyped virus, SARS-CoV-2 pseudotyped virus could efficiently infect certain cell lines including three human cell lines (293T-hACE2, 293T, and Huh-7) and three non-human primate cell lines (Vero, VeroE6, and LLC-MK2). As such, we selected these four out of the six cell lines in subsequent experiments, including 293T-hACE2, Huh-7, Vero, and LLC-MK2.Figure 2Selection of Susceptible Cell LinesA total of 26 different cell lines were infected with pseudotyped viruses with either SARS-CoV-2 S (A) or VSV G (B). The infected cell lysates were diluted by 10× and analyzed for luminescence activities (RLU). All results were obtained from three independent experiments (mean ± SEM). When the RLU for the tested cell reached 1% of that for Huh-7, it was deemed as a permissive cell line. The dash line indicates the 1% RLU value of Huh-7 cell. We first tested the infectivity of 106 pseudotyped viruses (80 natural variants and 26 glycosylation mutants) in 293T-hACE2 cells, where a difference by 4-fold in RLU compared with the reference Wuhan-1 strain (GenBank: MN_908947) was deemed as being significant ([Figure S1](#figs1){ref-type="fig"} ). Of all 106 pseudotyped viruses, 24 were determined as low-infectivity (17 natural mutants and 7 glycosylation mutants), with RLU reading decreased by 4- to 100-fold ([Figure S1](#figs1){ref-type="fig"}). Among them, 13 were located in the RBD region. Variant V341I and investigational glycosylation mutant (N331Q+N343Q) were deemed as no-infectivity as demonstrated by over 100-fold decrease in RLU values compared with the reference strain. Both of them were located in RBD. It is worth noting that double glycosylation deletions at N331 and N343 resulted in a drastic reduction in viral infectivity (1,200-fold), whereas single deletion at each site caused modest reduction in viral infectivity, with the infectivity of N331Q reduced by only 3-fold and N343Q by 20-fold. Moreover, the non-natural double glycosylation mutations in RBD (N331Q and N343Q) resulted in significantly reduced infectivity, suggesting that the two glycosylation sites in the RBD region may participate in the binding of the receptor or maintain the conformation of the RBD region.Figure S1Infectivity Analysis of Variants and Mutants in 293T-ACE2 Cell, Related to [Figure 3](#fig3){ref-type="fig"}RLU values resulting from infection with variant pseudotyped viruses were quantified by luminescence meter and normalized to the reference strain (Wuhan-1) produced in parallel, with the difference by 4-fold being considered as significant; all experiments were conducted three times (mean ± SEM) unless specified. The horizontal dashed lines indicate the threshold of 4-fold difference. The remaining 63 variants were tested further with other three cell lines for infectivity. Notably, single D614G and combined variants with D614G (D614G+L5F, D614G+V341I, D614G+K458R, D614G+I472V, D614G+D936Y, D614G+S939F, and D614G+S943T) demonstrated increased infectivity compared to the reference strain in all the four cell lines ([Figures 3](#fig3){ref-type="fig"}A--3D), whereas no difference was found between single D614G and D614G combined variants, suggesting that the enhanced infectivity was more likely ascribed to D614G itself.Figure 3Infectivity Analysis of Variants and Deletions of the Glycosylation Site MutantsInfectivity of natural variants and experimental mutants conducted in 293T-ACE2 (A), Huh-7 (B), Vero (C), and LLC-MK2 (D). RLU values generated with the infection of the variants or mutants, as measured by luminescence meter, were compared with the reference strain (Wuhan-1). A difference by 4-fold is considered significant; all experiments were conducted three times (mean ± SEM) unless specified. See also [Figure S1](#figs1){ref-type="fig"}. Differential Antigenicity of Natural Variants and Experimental Mutants with Monoclonal Antibodies {#sec2.3} ------------------------------------------------------------------------------------------------- Having identified the variants with altered infectivity, we next set out to investigate the antigenicity of the infectious mutants using 13 neutralizing monoclonal antibodies (mAbs) (see [STAR Methods](#sec4){ref-type="sec"}). It was noted that some changes in RBD region demonstrated altered sensitivity to neutralizing mAbs ([Figures 4](#fig4){ref-type="fig"} and [S2](#figs2){ref-type="fig"} ). Specifically, A475V reduced the sensitivity to mAbs 157, 247, CB6, P2C-1F11, B38, and CA1, whereas F490L reduced the sensitivity to mAbs X593, 261-262, H4, and P2B-2F6. Moreover, V483A became resistant to mAbs X593 and P2B-2F6, and L452R to mAbs X593 and P2B-2F6. Finally, Y508H reduced the sensitivity to mAb H014, N439K to mAb H00S022, A831V to mAb B38, D614G+I472V to mAb X593, and D614G+A435S to mAb H014 by more than 4 times. In addition, some changes in the RBD region, including V367F, Q409E, Q414E, I468F, I468T, Y508H, and A522V, were observed to be more susceptible to neutralization mediated by mAbs.Figure 4Analyses of Antigenicity of the Natural Variants and Experimental Mutants Using a Panel of Neutralizing mAbsSerial dilutions of mAb preparations were pre-incubated with the pseudotyped viruses at 37°C for 1 h before they were added to Huh-7 cells. Luciferase activity was measured 24 h later to calculate EC~50~ of each antibody. The ratio of EC~50~ between the variant or mutant strains and the reference strain (Wuhan-1) was calculated and analyzed to generate heatmap using Hem I ([@bib5]). The data were the results from 3--5 replicates. The red and blue boxes indicate the increase or decrease of the neutralization activity as shown in the scale bar. See also [Figure S2](#figs2){ref-type="fig"}.Figure S2Analyses of Antigenicity of Natural Variants and Experimental Mutants Using a Panel of Neutralizing mAbs, Related to [Figure 4](#fig4){ref-type="fig"}Serial dilutions of mAb preparations were pre-incubated with the virus at 37°C for one hour before they were added to Huh-7 cells. Luciferase activity was measured 24 hours later to calculate EC~50~ of each antibody. The y axis represents the ratio of EC~50~ between the variant/mutant strain and the reference strain (Wuhan-1). The data (mean ± SEM) were the results from 3-5 replicates. The vertical dashed lines indicate the threshold of 4-fold difference. The significant changes were marked with colored symbols, blue for decreased, red for increased. We next determine how infectious glycosylation mutants reacted to the same panel of mAbs. Mutant N165Q actually became more sensitive to mAb P2B-2F6, whereas N234Q reduced the neutralization sensitivity to different set of mAbs including 157, 247, CB6, P2C-1F11, H00S022, B38, AB35, and H014. These results confirmed that these two glycosylation sites are important for receptor binding. These mAbs have proven to be valuable in our analyses of the amino acid changes. As shown in [Figure 4](#fig4){ref-type="fig"}, five mAbs (i.e., 157, 247, CB6, P2C-1F11 and B38) were unable to effectively neutralize both A475V and N234Q. Neither X593 nor P2B-2F6 was effective in neutralizing L452R, V483A, and F490L, whereas P2B-2F6 was more effective in neutralizing N165Q. In addition, mAb H014 was incapable of neutralizing N234Q, Y508H, and D614G+A435S, whereas mAbs H4 and 261-262 were found not to neutralize F490L. Furthermore, H00S022 was unable to neutralizing N439K and N234Q. Altered Reactivity of Natural Variants and Experimental Mutants to Human Convalescent Sera {#sec2.4} ------------------------------------------------------------------------------------------ Finally, we determined the sensitivity of the strains with amino acid changes to ten COVID-19 convalescent sera (see [STAR Methods](#sec4){ref-type="sec"}). None of the variants and mutants demonstrated significantly altered sensitivity to all 10 convalescent sera, i.e., the EC~50~ values were not altered by more than 4-fold, irrespective of an increase or decrease, when compared with the reference strain ([Figures 5](#fig5){ref-type="fig"} A and [S3](#figs3){ref-type="fig"} ). However, the neutralization sensitivity of both F490L and H519P to three of ten patient sera were found to have decreased by more than 4 times, while six variants and mutants (N149H, N149Q, N165Q, N354D, N709Q, and N1173Q) became over 4-fold sensitive to one or two of the ten tested sera. Notably, five out of the six were glycan deletion mutants.Figure 5Differential Sensitivity of the Natural Variants and Experimental Mutants to a Panel of Convalescent Serum Samples(A) Serial dilutions of 10 patient serum samples were individually mixed with the pseudotyped viruses at 37°C for 1 h before added to Huh-7 cells for incubation of 24 h to determine the EC~50~. The experiments were repeated at least 3 times. Hem I software was used to analyze the data and draw the heatmap. The red and blue boxes indicate the increase or decrease of the neutralization activity as shown in the scale bar.(B) Summary of the data from ten serum samples, with the values presented as mean ± SEM. The horizontal dashed lines indicate the threshold of 4-fold difference. ^∗^p \< 0.05, ^∗∗^p \< 0.01, ^∗∗∗^p \< 0.005, ^∗∗∗∗^p \< 0.001.See also [Figure S3](#figs3){ref-type="fig"}.Figure S3Analyses of Antigenicity of the Natural Variants and Experimental Mutants Using Ten Convalescent Serum Samples, Related to [Figure 5](#fig5){ref-type="fig"}The data (mean ± SEM) were the results from 3-5 replicates. The vertical dashed lines indicate the threshold of 4-fold difference. The significant changes were marked with colored symbols, blue for decreased, red for increased. As shown in [Figure 5](#fig5){ref-type="fig"}B, when the data of individual convalescent sera were pooled together to analyze the sensitivity of all variants, no marked difference was observed (\>4-fold). However, modest differences between some variants and reference strain (within 4-fold) were observed in their reactivity to grouped convalescent sera. These differences were statistically significant (p \< 0.05). It is worth mentioning that some variants including F338L, V367F, I468F, I468T, and V615L ([Figure 5](#fig5){ref-type="fig"}B) were even more sensitive to the convalescent sera compared with reference strain, whereas more variants were found to be resistant to the convalescent sera. These variants include single amino acid change such as Y145del, Q414E, N439K, G446V, K458N, I472V, A475V, T478I, V483I, F490L, and A831V, as well as the double amino acid changes including D614G+Q321L, D614G+I472V, D614G+A831V, D614G+A879S and D614G+M1237I. Similar to natural variants, although the magnitude of some glycosylation deletions in sensitivity to the sera is less than 4-fold, the differences between mutants and the reference strain (Wuhan-1) were found to be still several-fold and statistically significant, i.e., glycosylation mutants N331Q and N709Q significantly increased the sensitivity to convalescent sera ([Figure 5](#fig5){ref-type="fig"}B). Discussion {#sec3} ========== As an RNA virus, SARS-CoV-2 virus is expected to continue evolving over time in human populations. Close monitoring of circulating virus strains is of unquestionable importance to inform research and development of vaccines and therapeutics. Here, we analyzed all spike sequences (over 13,000) reported to GISAID database. After filtering out incomplete, redundant, and ambiguous sequences, we narrowed down to 80 variants. Moreover, as glycosylation of viral protein is well documented to affect viral replication and immune response and SARS-CoV-2 S protein is heavily glycosylated, we also made 26 substitutional mutations at all 22 putative glycosylation sites. In total, we made 106 pseudotyped viruses, allowing us to characterize them using the established method ([@bib25]; see [STAR Methods](#sec4){ref-type="sec"}). [Table 1](#tbl1){ref-type="table"} summarizes the characteristics of variants and investigational mutants. Of all variants, D614G is of particular note. This variant has been shown to rapidly accumulating since its emergence and linked to more clinical presentations ([@bib17]). At the beginning of this study (May 6, 2020), it accounted for 62.8% ([Table S1](#mmc1){ref-type="supplementary-material"}) of all circulating strains, but by July 3, it had reached 75.7%. This dominant strain could effectively infect the four cell lines tested, being 10-fold more infectious than the original Wuhan-1 strain ([Figure 3](#fig3){ref-type="fig"}).Table 1Characteristics of Variants and MutantsGroup AGroup BGroup CNumber of variants or mutants295126Increased infectivityD614G, D614G+L5F, D614G+D936Y, D614G+S939F, D614G+S943TD614G+V341I, D614G+K458R, D614G+I472V[a](#tblfn1){ref-type="table-fn"}noneDecreased infectivityQ239K, D839Y, P1263L, D614G+Q675HV341I, D364Y, 385-387del, D405V, Q414P, I434K, S438F, D467V, P491R, V503F, R509K, V510L, P521SN122Q, N343Q, N717Q, T719A, N801Q, N1074Q, N331Q+N343QIncreased sensitivity to neutralizing mAbsnoneV367F, Q409E, Q414E, I468F, I468T, Y508H, A522VN165Q, N709QDecreased sensitivity to neutralizing mAbsA831VN439K, L452R, A475V, V483A, F490L, Y508H, D614G+A435S, D614G+I472V[a](#tblfn1){ref-type="table-fn"}N234QIncreased sensitivity to convalescent seraV615LF338L, V367F, I468F, I468TN149H, N149Q, N165Q, N331Q, N354D, N709Q, N1173QDecreased sensitivity to convalescent seraY145del, A831V, D614G+A831V, D614G+A879S, D614G+M1237IQ414E, N439K, G446V, K458N, I472V, A475V, T478I, V483I, F490L, H519P, D614G+Q321L, D614G+I472V[a](#tblfn1){ref-type="table-fn"}none[^3] Another important finding is that natural variants capable of affecting the reactivity to neutralizing mAbs were almost all located in the RBD region (except A831V) because all antibodies used in this study were targeting the RBD ([@bib2]; [@bib15]; [@bib24]; [@bib30]). Specifically, P2B-2F6 and P2C-1F11 were obtained using RBD as a bait to isolate RBD-specific B cells in peripheral blood mononuclear cells (PBMCs) of SARS-CoV-2 patients ([@bib15]). P2C-1F11 and P2B-2F6 actually bind to overlapping epitope, with the latter being better characterized. Specifically, P2B-2F6 is involved in three hydrophobic interaction sites on RBD (Y449, L452, and F490) ([Figures 6](#fig6){ref-type="fig"}A and 6B). Indeed, both L452R and F490L were natural variants, with decreased sensitivity to neutralization by P2B-2F6 mAb; because both L452R and F490L remain sensitive to P2C-1F11, suggesting this mAb is not derived from the same clone for P2B-2F6. Moreover, both mutants displayed decreased sensitivity to another neutralizing mAb X593 by 10-fold compared with the reference strain ([Figure 4](#fig4){ref-type="fig"}).Figure 6mAb Epitopes and Antigenicity-Related Sites(A and B) Epitope of the mAb P2B-2F6 on the trimer (A) and RBD (B).(C and D) Epitope of the mAb CB6 on the trimer (C) and RBD (D).(E and F) Epitope of the mAb H014 on the trimer (E) and RBD (F).The monoclonal antibody epitope is indicated in purple. The glycosylation sites are indicated in light blue. The sugar chain is shown in orange. The amino acid sites that coincide with the epitopes of monoclonal antibodies are indicated in green. Amino acid sites that do not coincide with the monoclonal antibody epitope are indicated in dark blue. Although we identified multiple variants with decreased sensitivity to neutralizing mAbs, we need to look at how frequent these variants are in the field. V483A in RBD is one of the two variants with a mutation frequency of over 0.1%. It showed decreased reactivity to the two mAbs (P2B-2F6 and X593) ([Figures 6](#fig6){ref-type="fig"}A and 6B; [@bib15]). Another RBD variant A475V sits in the binding epitope of RBD. It is significantly resistant to several neutralizing mAbs including P2C-1F11, CA1, 247, and CB6. It is noteworthy that CB6 mAb targets the receptor binding epitope ([Figures 6](#fig6){ref-type="fig"}C and 6D; [@bib30]). Specifically, Y508 was buried in the epitope targeted by mAb H014 ([Figures 6](#fig6){ref-type="fig"}E and 6F; [@bib24]). Indeed, the Y508H was found to be resistant to this mAb. It is worth mentioning that D614G+I472V has shown increased infectivity and more resistance to neutralizing antibodies ([Table 1](#tbl1){ref-type="table"}), but only one sequence (originated from Canada) was reported in GISAID. Moreover, some variants, including N439K, L452R, A475V, V483A, F490L, and Y508H, do have decreased sensitivity to neutralizing mAbs. However, only V483A exceeded 0.1% in frequency at the beginning of the study, all of which were found in the United States, with 28 sequences reported as of May 6, 2020, and 36 up to July 3, 2020. Variants containing N439K showed a significant increase in circulation, i.e., with 5 cases reported as of May 6, 2020 (all in the United Kingdom) to 47 by July 3, 2020 (45 in the United Kingdom and 2 in Romania). In addition, only one sequence from France containing Y508H was deposited in GIRSAID as of May 6, whereas four sequences reported as of July 3, 2020, of which two originated from Netherlands, one from Sweden, and one from France. Only one or two isolates were reported for other variants, which have not been observed to have increased during the time frame we have been monitoring. Nevertheless, as RNA viruses mutate all the time and some variants may only appears during certain period of time, whereas others could emerge in an unpredictable fashion, continued analyses of the circulating strains in terms of the mutation frequency and temporal pattern are warranted. Our results suggest that the 13 mAbs used in this study could be divided into seven groups, because they appear to be different in the inhibitory effects on the variants. As such, it would be interesting to formulate a therapeutic regimen comprised of at least two mAbs. For example, a combination of P2C-1F11 and X593 should be effective to inhibit all variants in this study. It would be of interest to test more neutralizing antibodies that could be targeting epitopes outside RBD. With regard to the glycosylation mutants analyzed in this study, N165Q increased the sensitivity to mAb P2b-2F6 whereas N234Q displayed resistance to neutralizing mAbs such CA1, CB6, 157, and others. Although neither of them is found in circulation, the reactivity of these two mutants to neutralizing mAb is still worth noting. As N165 and N234 are located near the RBD region ([@bib40]), these mutants may affect some epitopes targeted by neutralizing mAbs. Specifically, N165 glycosylation site is involved in the binding of mAb to the RBD region of S protein ([@bib2]). It is likely that the sugar chain can mask the epitope targeted by the antibody. This type of glycan shield has been observed in other viruses such as HIV-1. Specifically, the deletion of the N197 sugar chain of HIV-1 gp120 could enhance neutralization by targeting this epitope ([@bib22]; [@bib33]; [@bib37]). In this study, the other glycosylation mutant N234Q, which is also close to the RBD, is resistant to several mAbs. Nevertheless, we cannot exclude the possibility that the sugar chains themselves are the targets of the neutralizing mAbs, similar to observations made in other viruses. Specifically, the sugar chain at residues 142 and 144 in influenza virus H1N1 is essential for the induction of neutralizing antibodies ([@bib13]), while the broadly neutralizing antibodies against the epitopes of HIV-1 gp120, 2G12, PGT121, and PG9 have been found to target the sugar chains ([@bib7]). Because COVID-19 vaccines are being developed in different platform such as bacteria, mammalian cells, and plant expression systems, it is important to consider that different glycosylation profiles could affect the immunogenicity of the vaccines. The use of sera from 10 convalescent patients in neutralizing assay largely confirmed the results obtained with the well-characterized neutralizing mAbs. It is understood that the magnitude of altered reactivity is slightly smaller with human sera than that with mAbs, given that polyclonal antibodies from convalescent patents are directed against multi-epitopes on the full-length S protein; as a result, these polyclonal antibodies could complement one another. However, the differences in their reactivity to the human antibodies were found to be by several fold in most cases and all determined as statistically significant. Notably, some RBD variants such as A475V and F490L have been confirmed to have decreased sensitivity to both human sera and multiple neutralizing mAbs. A475V reduced the sensitivity to 6 mAb out of the 13 mAb used in this study, whereas F490L reduced the sensitivity to neutralization by 3 mAbs. It is possible that antibodies in convalescent sera are able to neutralize these critical epitopes targeted by these mAbs that are known to disrupt the binding of the S protein to hACE2 receptor ([@bib15]; [@bib30]; [@bib36]; [@bib39]). The A475V could weaken the hydrogen bond and hydrophobic interaction ([@bib30]), whereas F490L may erode the hydrophobic interaction between molecules ([@bib15]). In summary, we have analyzed over 100 pseudotyped viruses in terms of their infectivity and sensitivity to neutralization by well-characterized mAbs or human sera from convalescent patients. Amino acid changes have been observed across the entire spike protein. An amino acid change (D614G) outside the RBD was found to be more infectious, but no evidence of being resistant to neutralizing antibodies has been demonstrated. However, the increasing dominance of D614G particularly deserves attention. Although some strains with amino acid changes at RBD studied here lost their infectivity, suggesting they may not likely become widespread, the RBD natural variants with increased resistance to antibody-mediated neutralization should be closely watched. Moreover, ablation of glycosylation sites affected their reactivity to neutralizing antibodies, along with their infectivity, enforcing the notion that the glycan could substantially affect SARS-CoV-2 viral replication and vaccine-induced immune responses. Collectively, our findings help shed light on the implications of some evolving strains in circulating viruses with respect to enhanced infectivity and altered antigenicity. STAR★Methods {#sec4} ============ Key Resources Table {#sec4.1} ------------------- REAGENT or RESOURCESOURCEIDENTIFIER**Antibodies**X593Laboratory of X. Sunney XieN/ACA1Laboratory of Jinghua Yan; [@bib30]N/ACB6Laboratory of Jinghua Yan; [@bib30]N/AH014Laboratory of Dr. Liangzhi XieN/AH00S022Laboratory of Dr. Liangzhi XieN/AP2C-1F11Laboratory of Linqi Zhang; [@bib15]N/AP2B-2F6Laboratory of Linqi Zhang; [@bib15]N/AAB35Laboratory of Linqi ZhangN/A261-262Laboratory of Linqi ZhangN/A157Laboratory of Linqi ZhangN/A247Laboratory of Linqi ZhangN/AH4Laboratory of Fu Gao; [@bib42]N/AB38Laboratory of Fu Gao; [@bib42]N/A**Bacterial and Virus Strains**DH5α Chemically Competent CellInvitrogenCat\#12034013G^∗^ΔG-VSVKerafastCat\#EH1020-PM**Biological Samples**Convalescent patient serum, CS1This paperN/AConvalescent patient serum, CS2This paperN/AConvalescent patient serum, CS3This paperN/AConvalescent patient serum, CS4This paperN/AConvalescent patient serum, CS6This paperN/AConvalescent patient serum, CS7This paperN/AConvalescent patient serum, CS8This paperN/AConvalescent patient serum, CS10This paperN/AConvalescent patient serum, CS86This paperN/AConvalescent patient serum, CS87This paperN/A**Critical Commercial Assays**Britelite plus reporter gene assay systemPerkinElmerCat\#6066769**Experimental Models: Cell Lines**293TATCCCat\#CRL-3216; RRID: CVCL_0063293T-hACE2Sino Biological CompanyN/AA549ATCCCat\#CCL-185; RRID: CVCL_0023BHK21ATCCCat\#CCL-10; RRID: CVCL_1915Cf2THATCCCat\#CRL-1430; RRID: CVCL_3363CHOATCCCat\#CCL-61; RRID: CVCL_0214CRFKATCCCat\#CCL-94; RRID: CVCL_2426DC2.4MilliporeCat\#SCC142; RRID: CVCL_J409HeLaATCCCat\#CCL-2; RRID: CVCL_0030HepG2ATCCCat\#HB-8065; RRID: CVCL_0027Huh-7JCRBCat\#0403; RRID: CVCL_0336JASWIIATCCCat\#CRL-11904; RRID: CVCL_3727_K562ATCCCat\#CCL-243; RRID: CVCL_0004LLC-MK2ATCCCat\#CCL-7; RRID: CVCL_3009MDBKATCCCat\#CCL-22;; RRID: CVCL_0421MDCKATCCCat\#CCL-34; RRID: CVCL_0422MdKiLaboratory of Dr. Zhengli Shi; [@bib43]N/AMRC-5ATCCCat\#CCL-171; RRID: CVCL_0440Mv 1 LuATCCCat\#CCL-64; RRID: CVCL_0593PK15ATCCCat\#CCL-33; RRID: CVCL_2160RAW264.7ATCCCat\#TIB-71; RRID: CVCL_0493RlKiTLaboratory of Dr. Zhengli Shi; [@bib43]N/ASK-N-MCATCCCat\#HTB-10; RRID: CVCL_0530STATCCCat\#CRL-1746; RRID: CVCL_2204VeroATCCCat\#CCL-81; RRID: CVCL_0059VeroE6ATCCCat\#CRL-1586; RRID: CVCL_0574**Oligonucleotides**VSV (P protein)-F:TCTCGTCTGGATCAGGCGGGENEWIZN/AVSV (P protein)-R: TGCTCTTCCACTCCA\ TCCTCTTGGGENEWIZN/APrimers design for mutagenesis were located in [Table S2](#mmc2){ref-type="supplementary-material"}N/AN/A**Recombinant DNA**Plasmid:pcDNA3.1.S2 (codon-optimized S gene of SARS-CoV-2, GenBank: [MN_908947](ncbi-n:MN_908947){#interref60})[@bib25]Addgene ID: [149457](ncbi-tnm:149457){#intref0015}Plasmid:pcDNA3.1.S2-L5FThis paperN/APlasmid:pcDNA3.1.S2-L8VThis paperN/APlasmid:pcDNA3.1.S2-L8WThis paperN/APlasmid:pcDNA3.1.S2-H49YThis paperN/APlasmid:pcDNA3.1.S2-Y145delThis paperN/APlasmid:pcDNA3.1.S2-Q239KThis paperN/APlasmid:pcDNA3.1.S2-F338LThis paperN/APlasmid:pcDNA3.1.S2-V341IThis paperN/APlasmid:pcDNA3.1.S2-A348TThis paperN/APlasmid:pcDNA3.1.S2-N354DThis paperN/APlasmid:pcDNA3.1.S2-N354KThis paperN/APlasmid:pcDNA3.1.S2-S359NThis paperN/APlasmid:pcDNA3.1.S2-D364YThis paperN/APlasmid:pcDNA3.1.S2-V367FThis paperN/APlasmid:pcDNA3.1.S2-K378RThis paperN/APlasmid:pcDNA3.1.S2-P384LThis paperN/APlasmid:pcDNA3.1.S2-385-387delThis paperN/APlasmid:pcDNA3.1.S2-D405VThis paperN/APlasmid:pcDNA3.1.S2-R408IThis paperN/APlasmid:pcDNA3.1.S2-Q409EThis paperN/APlasmid:pcDNA3.1.S2-Q414EThis paperN/APlasmid:pcDNA3.1.S2-Q414PThis paperN/APlasmid:pcDNA3.1.S2-I434KThis paperN/APlasmid:pcDNA3.1.S2-A435SThis paperN/APlasmid:pcDNA3.1.S2-S438FThis paperN/APlasmid:pcDNA3.1.S2-N439KThis paperN/APlasmid:pcDNA3.1.S2-G446VThis paperN/APlasmid:pcDNA3.1.S2-L452RThis paperN/APlasmid:pcDNA3.1.S2-K458RThis paperN/APlasmid:pcDNA3.1.S2-K458NThis paperN/APlasmid:pcDNA3.1.S2-D467VThis paperN/APlasmid:pcDNA3.1.S2-I468FThis paperN/APlasmid:pcDNA3.1.S2-I468TThis paperN/APlasmid:pcDNA3.1.S2-I472VThis paperN/APlasmid:pcDNA3.1.S2-A475VThis paperN/APlasmid:pcDNA3.1.S2-G476SThis paperN/APlasmid:pcDNA3.1.S2-T478IThis paperN/APlasmid:pcDNA3.1.S2-V483AThis paperN/APlasmid:pcDNA3.1.S2-V483IThis paperN/APlasmid:pcDNA3.1.S2-F490LThis paperN/APlasmid:pcDNA3.1.S2-P491RThis paperN/APlasmid:pcDNA3.1.S2-V503FThis paperN/APlasmid:pcDNA3.1.S2-Y508HThis paperN/APlasmid:pcDNA3.1.S2-R509KThis paperN/APlasmid:pcDNA3.1.S2-V510LThis paperN/APlasmid:pcDNA3.1.S2-H519QThis paperN/APlasmid:pcDNA3.1.S2-H519PThis paperN/APlasmid:pcDNA3.1.S2-A520SThis paperN/APlasmid:pcDNA3.1.S2-P521SThis paperN/APlasmid:pcDNA3.1.S2-A522SThis paperN/APlasmid:pcDNA3.1.S2-A522VThis paperN/APlasmid:pcDNA3.1.S2-D614GThis paperN/APlasmid:pcDNA3.1.S2-V615LThis paperN/APlasmid:pcDNA3.1.S2-A831VThis paperN/APlasmid:pcDNA3.1.S2-D839EThis paperN/APlasmid:pcDNA3.1.S2-D839YThis paperN/APlasmid:pcDNA3.1.S2-D936YThis paperN/APlasmid:pcDNA3.1.S2-S943TThis paperN/APlasmid:pcDNA3.1.S2-S943RThis paperN/APlasmid:pcDNA3.1.S2-G1124VThis paperN/APlasmid:pcDNA3.1.S2-P1263LThis paperN/APlasmid:pcDNA3.1.S2-Y145del+R408IThis paperN/APlasmid:pcDNA3.1.S2-D614G+L5FThis paperN/APlasmid:pcDNA3.1.S2-D614G+Q239KThis paperN/APlasmid:pcDNA3.1.S2-D614G+Q321LThis paperN/APlasmid:pcDNA3.1.S2-D614G+V341IThis paperN/APlasmid:pcDNA3.1.S2-D614G+A435SThis paperN/APlasmid:pcDNA3.1.S2-D614G+K458RThis paperN/APlasmid:pcDNA3.1.S2-D614G+I472VThis paperN/APlasmid:pcDNA3.1.S2-D614G+H519PThis paperN/APlasmid:pcDNA3.1.S2-D614G+Q675HThis paperN/APlasmid:pcDNA3.1.S2-D614G+A831VThis paperN/APlasmid:pcDNA3.1.S2-D614G+A845SThis paperN/APlasmid:pcDNA3.1.S2-D614G+A879SThis paperN/APlasmid:pcDNA3.1.S2-D614G+D936YThis paperN/APlasmid:pcDNA3.1.S2-D614G+S939FThis paperN/APlasmid:pcDNA3.1.S2-D614G+S943TThis paperN/APlasmid:pcDNA3.1.S2-D614G+M1229IThis paperN/APlasmid:pcDNA3.1.S2-D614G+M1237IThis paperN/APlasmid:pcDNA3.1.S2-D614G+P1263LThis paperN/APlasmid:pcDNA3.1.S2-N17QThis paperN/APlasmid:pcDNA3.1.S2-N61QThis paperN/APlasmid:pcDNA3.1.S2-N74QThis paperN/APlasmid:pcDNA3.1.S2-N122QThis paperN/APlasmid:pcDNA3.1.S2-N149QThis paperN/APlasmid:pcDNA3.1.S2-N165QThis paperN/APlasmid:pcDNA3.1.S2-N234QThis paperN/APlasmid:pcDNA3.1.S2-N282QThis paperN/APlasmid:pcDNA3.1.S2-N331QThis paperN/APlasmid:pcDNA3.1.S2-N343QThis paperN/APlasmid:pcDNA3.1.S2-N603QThis paperN/APlasmid:pcDNA3.1.S2-N616QThis paperN/APlasmid:pcDNA3.1.S2-N657QThis paperN/APlasmid:pcDNA3.1.S2-N709QThis paperN/APlasmid:pcDNA3.1.S2-N717QThis paperN/APlasmid:pcDNA3.1.S2-N801QThis paperN/APlasmid:pcDNA3.1.S2-N1074QThis paperN/APlasmid:pcDNA3.1.S2-N1098QThis paperN/APlasmid:pcDNA3.1.S2-N1134QThis paperN/APlasmid:pcDNA3.1.S2-N1158QThis paperN/APlasmid:pcDNA3.1.S2-N1173QThis paperN/APlasmid:pcDNA3.1.S2-N1194QThis paperN/APlasmid:pcDNA3.1.S2-N74KThis paperN/APlasmid:pcDNA3.1.S2-N149HThis paperN/APlasmid:pcDNA3.1.S2-T719AThis paperN/APlasmid:pcDNA3.1.S2-N331Q+N343QThis paperN/A**Software and Algorithms**GraphPad Prism version 8.0.1(244)GraphPad Software<https://www.graphpad.com>Microsoft Office Home and Student 2019Microsoft Corporation<https://www.microsoft.com/microsoft-365>Heatmap Illustrator (HemI) version 1.0.3.7[@bib5]<http://ccd.biocuckoo.org>BioEdit version 7.2BioEidt Software<https://bioedit.software.informer.com>Adobe Illustrator CC 2018Adobe<https://www.adobe.com> Resource Availability {#sec4.2} --------------------- ### Lead Contact {#sec4.2.1} Further information and requests for resources and reagents should be directed to and will be fulfilled by the Lead Contact, Dr. Youchun Wang (<wangyc@nifdc.org.cn>). ### Materials Availability {#sec4.2.2} All the unique reagents generated in this study are available from the Lead Contact with a completed Materials Transfer Agreement. ### Data and Code Availability {#sec4.2.3} This study did not generate any unique datasets or code. Experimental Models and Subject Details {#sec4.3} --------------------------------------- ### Cell lines {#sec4.3.1} Most cell lines were cultured in Dulbecco's modified Eagle medium (DMEM, high glucose; Hyclone, Cat\#SH30243.01). They include 293T(*Homo sapiens*, embryonic kidney), 293T-hACE2 (293T cells stably expressed hACE2), A549 (*Homo sapiens*, liver), BHK21 (*Mesocricetus auratus*, kidney), Cf2TH (*Canis familiaris*, thymus), CHO (*Cricetulus griseus*, ovary), CRFK (*Felis catus*, kidney), HeLa (*Homo sapiens*, cervix), HepG2 (*Homo sapiens*, liver), Huh-7 (*Homo sapiens*, liver, gallbladder), LLC-MK2 (*Macaca mulatta*, kidney), MDBK (*Bos taurus*, kidney), MDCK (*Canis familiaris*, kidney), MRC-5 (*Homo sapiens*, lung), MV1-Lu (Neovison vison, lung), PK15 (*Sus scrofa*, kidney), RAW264.7 (*Mus musculus*, leukemia, ascites), SK-N-MC (*Homo sapiens*, brain), ST (Sus scrofa, testis), Vero (Cercopithecus aethiops, kidney), and VeroE6 (*Cercopithecus aethiops*, kidney) cells. DC2.4 (*Mus musculus*, bone marrow derived dendritic cells), K562 (*Homo sapiens*, bone marrow) and MdKi (*Myotis davidii*, kidney) and cells were incubated in RPMI medium modified (Hyclone, Cat\#SH30809.01). RlKiT(R. leschenaultii, kidney) were cultured in DMEM/F-12, GlutaMAX (GIBCO, Cat\#10565-018). JASWII (*Mus musculus*, bone marrow) were cultured in MEMα, nucleosides (GIBCO, Cat\#12571063) with 5 ng/ml Recombinant Murine GM-CSF (Peprotech, Cat\#315-03). All the cells were cultured in media supplemented with 100 U/mL of Penicillin-Streptomycin solution (GIBCO, Cat\#15140163), 20mM N-2-hydroxyethylpiperazine-N-2-ethane sulfonic acid (HEPES, GIBCO, Cat\#15630080) and 10% fetal bovine serum (FBS, Pansera ES, PAN-Biotech GmbH, Cat\#ST30-2602), a humidified atmosphere with 5% CO~2~ at 37°C, with the exception of JASWII cells which were cultured in medium with 20% FBS. 0.25% Trypsin-EDTA (GIBCO, Cat\#25200056) were used to detach cells for subculture. ### Human sera {#sec4.3.2} Human serum samples from 10 convalescent patients in Wuhan (CS1, CS2, CS3, CS4, CS6, CS7, CS8 and CS10) and Shandong (CS86 and CS87) were collected on Feb 18, 2020 and Mar 5, 2020. All volunteers signed informed consent forms. Method Details {#sec4.4} -------------- ### Site-directed mutagenesis {#sec4.4.1} pcDNA3.1.S2 recombinant plasmid (GenBank: [MT_613044](ncbi-n:MT_613044){#interref65}), constructed by inserted the codon-optimized S gene of SARS-CoV-2 (GenBank: [MN_908947](ncbi-n:MN_908947){#interref70}) into pcDNA3.1 ([@bib25]), was used as the template to generate the plasmid with mutagenesises in S gene. Following procedure of circular PCR, 15 to 20 nucleotides before and after the target mutation site were selected as forward primers, while the reverse complementary sequences were selected as reverse primers. Following site-directed mutagenesis PCR, the template chain was digested using *Dpn*I restriction endonuclease (NEB, USA). Afterward, the PCR product was directly used to transform *E. coli* DH5α competent cells; single clones were selected and then sequenced. The primers designed for the specific mutation sites are listed in [Table S2](#mmc2){ref-type="supplementary-material"}, and the frequency of different variants in the epidemic population is listed in [Table S1](#mmc1){ref-type="supplementary-material"}. ### Production and titration of pseudotyped viruses {#sec4.4.2} Pseudotyped viruses incorporated with spike protein from either SARS-CoV-2, variants or mutants were constructed using a procedure described by us recently ([@bib25]). On day before transfection, 293T cells were prepared and adjusted to the concentration of 5 −7 × 10^5^ cell/ml, 15 mL of which were transferred into a T75 cell culture flask and incubated overnight at 37°C in an incubator conditioned with 5% CO~2~. The cells generally reach 70%--90% confluence after overnight incubation. Thirty microgram of DNA plasmid expressing the spike protein was transfected according to the user's instruction manual. The transfected cells were subsequently infected with G^∗^ΔG-VSV (VSV G pseudotyped virus) at concentration of 7.0 × 10^4^TCID50/ml. These cells were incubated at 37°C for 6-8 hours in the presence of in 5% CO~2~. Afterward, cell supernatant was discarded, followed by rinsing the cells gently with PBS +1% FBS. Next, 15ml fresh complete DMEM was added to the flask and cultured for 24 h. Twenty-four hours post infection, SARS-CoV-2 pseudotyped viruses containing culture supernatants were harvested, filtered (0.45-μm pore size, Millipore, Cat\#SLHP033RB) and stored at −70°C in 2 mL aliquots until use. The 50% tissue culture infectious dose (TCID50) of SARS-CoV-2 pseudovirus was determined using a single-use aliquot from the pseudovirus bank to avoid inconsistencies resulted from repeated freezing-thawing cycles. For titration of the pseudotyped virus, a 2-fold initial dilution with six replicates was made in 96-well culture plates followed by serial 3-fold dilutions. The last column was employed as the cells control without pseudotyped virus. Subsequently, the 96-well plates were seeded with Huh-7 cells adjusted to 2 × 10^5^cells/ml. After 24 h incubation at 37°C in a humidified atmosphere with 5% CO~2~, the supernatant was aspirated and discarded gently to leave 100 μL in each well; next, 100 μL of luciferase substrate (Perkinelmer, Cat\#6066769) was added to each well. After 2-min incubation at room temperature in the dark, 150 μL of lysate was transferred to white 96-well plates for the detection of luminescence using a luminometer (PerkinElmer, Ensight). Positive was determined to be ten-fold higher than the negative (cells only) in terms of relative luminescence unit (RLU) values. The 50% tissue culture infectious dose (TCID50) was calculated using the Reed--Muench method ([@bib25]). ### Quantification of pseudotyped virus particles using RT-PCR {#sec4.4.3} Before quantification, all the pseudotyped viruses were purified through a 25% sucrose cushion by ultra-centrifugation at 100,000 × g for 3 h ([@bib25]). Viral RNA was extracted from 140 μL of purified pseudotyped viruses using the QIAamp Viral RNA Mini Kit (QIAGEN, Cat\#52906), and served as template for reverse transcription using the SuperScript III First-Strand Synthesis System for RT-PCR kit reagent (Invitrogen, Cat\#18080-051). Virus quantification by real-time PCR was performed using the TB Green Premix Ex TaqII (TaKaRa, Cat\#RR820A), following the supplier's instruction. The P protein gene of VSV virus was cloned into the vector pCDNA3.1(+) as a plasmid standard, with the viral copy number calculated accordingly. See primers in the [Key Resources Table](#sec4.1){ref-type="sec"}. ### Infection assay {#sec4.4.4} Using the quantitative RT-PCR, we normalized the pseudotyped virus particles to the same amount. After normalization, 100 μL of the pseudotyped virus with 10-fold dilution was added to wells in 96-well cell culture plate. After the cells were trypsin-digested, 2 × 10^4^/100 μL cells were added to each well in the 96-well plates. The plates were then incubated at 37°C in a humidified atmosphere with 5% CO~2~. After incubation for 24 hours, chemiluminescence detection was performed as described in the titration of pseudotyped viruses. Each group contained 3-5 replicates. ### Neutralization assay {#sec4.4.5} The virus neutralization assay was conducted as described previously ([@bib25]). Briefly, 100 μL serial dilutions of human sera or monoclonal antibody preparations were added into 96-well plates. After that, 50 μL pseudoviruses with concentration of 1300 TCID50/ml were added into the plates, followed by incubation at 37°C for 1 hour. Afterward, Huh-7 cells were added into the plates (2 × 10^4^ cells/100 μL cells per well), followed by incubation at 37°C in a humidified atmosphere with 5% CO~2~. Chemiluminescence detection was performed after 24 hours incubation. The Reed-Muench method was used to calculate the virus neutralization titer. The results are based on 3-5 replicates unless specified. In order to validate the test operation process, the Coefficient of Variance (CV) control of replicates is set within 30% of six wells, so is the CV for the duplicate sample wells. Quantification and Statistical Analysis {#sec4.5} --------------------------------------- GraphPad Prism 8 was used for plotting and statistical analysis; the values were expressed as mean ± SEM. One-way ANOVA and Holm-Sidak's multiple comparisons test was used to analyze the differences between groups. A p value of less than 0.05 was considered to be significant. ^∗^p \< 0.05, ^∗∗^p \< 0.01, ^∗∗∗^p \< 0.005, ^∗∗∗∗^p \< 0.001, ns represents no significant difference. Supplemental Information {#app2} ======================== Table S1. Rates of Variants, Related to Figure 1 Table S2. Primers Design for Mutagenesis, Related to Key Resources Table We would like to thank Prof. X. Sunney Xie of Peking University for providing mAb X593; Prof. JinghuaYan of the Institute of Microbiology, Chinese Academy of Sciences for mAbs CA1 and CB6; Dr. Liangzhi Xie from Sino Biological Company for mAbs H014 and H00S022 and the 293T-hACE2 cell line; Prof. Linqi Zhang of Tsinghua University for mAbs P2C-1F11, P2B-2F6, AB35, 261-262, 157, and 247; and Prof. Yan Wu of the Institute of Microbiology, Chinese Academy of Sciences for H4 and B38. We would like to thank Dr. Xiaoming Yang from China National Biotec Group Company Ltd. for providing convalescent sera (CS1, CS2, CS3, CS4, CS6, CS7, CS8, and CS10) and Ms. Fangyu Dong from China Biologic Products Holdings, Inc. for convalescent sera CS86 and CS87. This work was supported by the National Science and Technology Major Projects of Drug Discovery (2018ZX09101001), the National Science and Technology Major Projects of Infectious Disease (2017ZX10304402), and the 10.13039/100000865Bill and Melinda Gates Foundation (INV-006379). Author Contributions {#sec5} ==================== Y.W. and W.H. conceived, designed, and supervised the experiments. J.N., Li Zhang, Y.W., Xuguang Li, and W.H. wrote the manuscript. Q. Li, J.W., H.H., S.L., C.Z., H.L., H.Q., L.N., J.L., M.W., Q.S., Q. Lu, and Xiaoyu Li performed the experiments. Linqi Zhang and Q.Z. provided some mAbs and analyzed them. All of the authors have read and approved the final manuscript. Declaration of Interests {#sec6} ======================== The authors declare no competing interests. Supplemental Information can be found online at <https://doi.org/10.1016/j.cell.2020.07.012>. [^1]: These authors contributed equally [^2]: Lead Contact [^3]: D614G+I472V is the only variant with increased infectivity and decreased sensitivity to neutralizing mAb and convalescent sera. It is of note only one sequence is recorded in GISAID.
3.046875
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Although scientists are unable to definitively uncover all of the 944 chemical constituents in fracking fluid, they have been able to identify some of the more prominent pollutants. [Source: Earthworks] As expected the CDPHE report downplays the public health impacts from exposure to oil & gas operations and calls for more monitoring and analysis, rather than immediate public health action. “This report evaluates the existing science about whether you’re at risk if you live near oil and gas operations,” said Dr. Larry Wolk, executive director and chief medical officer at the department. “Going forward, we will continue to evaluate health risks using more comprehensive, relevant data currently being collected.” The health risk portion of the study combined more than 10,000 air quality samples to evaluate how 62 substances in those samples compare to an identified “safe” level for human exposure. The report concludes: The concentrations of a small number of substances (benzene, formaldehyde, acetaldehyde) in the air surrounding oil and gas operations are four to five times lower than standard health limits set for short- and long-term exposure. The concentrations of the other substances are five to 10,000 times lower than the standard health limits set for short- and long-term exposure. Cancer risks for all substances are within the “acceptable risk” range established by the U.S. Environmental Protection Agency. Overall, the current assessment suggests the risk of harmful health effects is low for residents living at distances 500 feet or more from oil and gas operations. How much of a chemical is present in an environmental medium (e.g., soil, water, air), How much contact (exposure) a person or ecological receptor has with the contaminated environmental medium, and The inherent toxicity of the chemical. Variability and uncertainly are two other important factors which must be considered. Variability refers to the range of toxic response or exposure since toxin exposures can affect individuals differently. Uncertainty refers to the lack of certain knowledge due to incomplete data because toxicology tests are usually conducted on laboratory rats, and not humans. For that reason it’s important for researchers to fill in the gaps by continuing to include more data. With the CDPHE’s acknowledgment that conclusions are based on “current assessments,” there appears to be some hope that the door has been opened a crack for further assessments. The report also reviewed 12 previous epidemiological studies that looked at potential health effects from living near oil and gas operations. Overall, the review concluded that studies of populations living near oil and gas operations provide limited evidence of the possibility for harmful health effects, which needs to be confirmed or disputed with higher-quality studies. The authors also developed evidence statements for each of the 27 health effects in these studies and found: No substantial or moderate evidence for any health effects. Limited evidence for two health effects: self-reported skin symptoms and exacerbation of asthma. Limited evidence means modest scientific findings that support an association, but there are significant limitations. Mixed evidence for 11 health effects, including four different birth outcomes; hematological childhood cancers; hospitalizations for cancer, migraines, self-reported respiratory symptoms and musculoskeletal symptoms; and hospitalizations for neurological and hematological/immune diseases. Mixed evidence means there are findings that both support and oppose an association between the exposure and the outcome, with neither direction dominating. A lack of evidence for three health effects, including respiratory hospitalizations and self-reported psychological symptoms and gastrointestinal symptoms. A lack of evidence means that the outcome has been researched without evidence of an association. All of the above emphasizes the need for more evidence and more research. As frustrating as it is for those of us living with the health impacts from oil & gas development my own experience and research has convinced me of the need for more evidence and more research. What I know for certain is that the human body responds to exposure from oil & gas operations according to individual DNA. More human health studies are needed and those studies must include individual DNA analysis, as well as blood and urine testing. Current health studies are based on the CDPHE’s public health data. We need studies based on individual human testing. Physicians should be encouraged to collect specific health data and report to the CDPHE. The report’s conclusions included in the Executive Summary reveal a recognition on the part of the CDPHE that the possibility for harmful health effects does indeed exist: Conclusions Based on currently available air monitoring data, the risk of harmful health effects is low for residents living near oil and gas operations. Studies of populations living near oil and gas operations provide limited evidence of the possibility for harmful health effects. This needs to be confirmed or disputed with higher quality studies. At this time, results from exposure and health effect studies do not indicate the need for immediate public health action, but rather indicate the need for more detailed exposure monitoring and systematic analyses of health effects of residents living near oil and gas operation. However the recommendations are specific and definitely the most significant part of this report: Recommendations Continued monitoring of exposures to people living near oil and gas including: Continued evaluation of ambient air levels of priority substances in areas with substantial oil and gas operations to assess the potential for community-wide health impacts. Collection of air samples in communities near oil and gas operations using our Colorado Air Mobile Monitoring Laboratory to better characterize short-term exposures for those living in close proximity to oil and gas oerations. Continued evaluation of health risk using more comprehensive exposure data such as data from the Colorado State University studies that directly measured emissions of substances from oil and gas operations in Garfield County and the north Front Range and data collected by the Colorado Air Mobile Monitoring Laboratory. Continued monitoring of health effects in areas with substantial oil and gas operations including: High-quality epidemiological studies with improved characterization of exposures to directly assess the possibility of health effects in communities with substantial oil and gas operations. Continued citizen reporting of health concerns to the CDPHE Oil and Gas Health Information and Response Program to monitor for trends in health effects that may be related to exposure. As someone who has been beating the drum of health impacts from oil and gas operations for more than a decade, I believe these recommendations represent progress, albeit deliberately slow, from CDPHE. I remember a time when Dr. Chris Urbina was at the helm, the official position when it came to oil & gas health impacts was “hear no evil, see no evil, speak no evil.” Total denial. The recognition of possible harm within the report’s conclusion and the list of specific recommendations are more “acknowledgment” than we’ve seen up till now. Moving forward, it will be up to the citizens of Colorado to put the pressure on the CDPHE to follow through with more monitoring, more evaluations, and more analysis. This report looked at existing data. The state health department currently is conducting a health-risk assessment specific to oil and gas emissions, using newly released data from Colorado State University. That study will be completed in 2018. One Comment on “CDPHE report recommends more monitoring and analysis for fracking health impacts” As the CDPHE study was not initiated until after so recommended by the Governor’s special scam I mean taskforce in 2015. which was at-least a year after the price of oil and natural gas had crashed. my guess is that the CDPHE findings are substantially below study findings from previous to the fall of 2014 entirely due to the greatly-reduced number of fracking rigs operating in Colorado. Before June of 2014 when the price of oil began to drop there were as many as 125 drilling rigs operating across Colorado, however, from the summer of 2015 through the summer of 2016 that number had been reduced to just 15-20 rigs operating, which would have caused air quality impacts to be substantially lessened. Given the fact that CDPHE doesn’t have the money to come out and investigate poor construction practices at the pipeline construction site near Battlement Mesa that have led to silt and sand runoff damage due to a lack of proper silt prevention, I question how the same organization could afford to do a thorough job with this study. With the State desperate for more fracking income thanks to TABOR, which gives the State a reason to falsify this study, I would feel much better about the study if it was peer-reviewed, considering that CDPHE has endlessly tried to poke holes in previous peer-reviewed science finding fault with fracking. I am also the owner of the Facebook page Coloradans for Responsible Energy and Environmental Policy in Broomfield
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Q: Variable does not change in python binary game Hi I am writing a binary game in Python and I don't know why the 2 variables left and right are changing. Here is what I have done so far: def guessNumberBasic(): n=101 left=0 right=n-1 guess=(left+right)//2 print("Please think of an integer between 1 and 100, but don’t tell me what it is.") while True: player_ans=input("Is it greater, equal to or less than "+ str(guess) + " (G/E/L)?") if player_ans=="E": break elif player_ans=="G": right=guess+1 elif player_ans=="L": left=guess+1 print("I guess you thought of ", guess," Am I right? I know I’m right.") the output: Is it greater, equal to or less than 50 (G/E/L)?G Is it greater, equal to or less than 50 (G/E/L)?G Is it greater, equal to or less than 50 (G/E/L)?G Is it greater, equal to or less than 50 (G/E/L)?G Is it greater, equal to or less than 50 (G/E/L)?L Is it greater, equal to or less than 50 (G/E/L)?E I guess you thought of 50 Am I right? I know I’m right thanks A: you are never changing the value of guess once you set it. You only then change the lsft and right value. Instead you should set guess at the start of each loop def guessNumberBasic(): n=101 left=0 right=n-1 print("Please think of an integer between 1 and 100, but don’t tell me what it is.") while True: guess = (left + right) // 2 player_ans=input("Is it greater, equal to or less than "+ str(guess) + " (G/E/L)?") if player_ans=="E": break elif player_ans=="G": left=guess+1 elif player_ans=="L": right=guess+1 print("I guess you thought of ", guess," Am I right? I know I’m right.") guessNumberBasic() OUTPUT Please think of an integer between 1 and 100, but don’t tell me what it is. Is it greater, equal to or less than 50 (G/E/L)?G Is it greater, equal to or less than 75 (G/E/L)?L Is it greater, equal to or less than 63 (G/E/L)?G Is it greater, equal to or less than 70 (G/E/L)?E I guess you thought of 70 Am I right? I know I’m right.
3.203125
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Researchers at Beth Israel Deaconess Medical Center are using artificial intelligence to identify images of bacteria quickly and accurately through an AI-enhanced microscope, which they contend has the potential to alleviate the current national shortage of clinical microbiologists. BIDMC’s Clinical Microbiology Laboratory is a “hidden part” of the Boston hospital, explains James Kirby, MD, director of the lab, but one that serves a critical function in diagnosing potentially deadly blood infections which is passed along to clinicians to determine appropriate therapies. “We have a microbiology technologist workforce, and one the things they spend a lot of time doing is looking at patient specimens in order to make a diagnosis of the type of infection people have,” says Kirby, who is also associate professor of pathology at Harvard Medical School. “That’s a very labor-intensive task. It takes time, and it takes a lot of skill.” However, Kirby notes that there is a nationwide shortage of highly trained microbiologists, with 9 percent of lab technologists positions remaining unfilled—a situation that will only get worse with 20 percent of technologists projected to reach retirement age during the next five years, according to the American Society for Clinical Pathology. To fill this gap, BIDMC researchers are leveraging an automated AI-enhanced microscope system from MetaSystems with a digital camera—which collects high-resolution image data—and so far has proven “highly adept” at identifying images of bacteria quickly and accurately based on their shape and distribution, according to Kirby. Researchers specifically trained a class of AI modeled on the mammalian visual cortex, called convolutional neural network (CNN), to analyze visual data from blood samples on microscopic slides in order to categorize bacteria in suspected bloodstream infections. “One characteristic of these convolutional neural networks is the more you train it, the better it becomes” at these tasks, observes Kirby, who says his research team generated more than 100,000 training images for the system. “It’s like a child going from primary to secondary school.” Results of a study, published recently in the Journal of Clinical Microbiology, show that the CNN was able to sort images into the three categories of bacteria—rod-shaped, round clusters and round chains or pairs—ultimately achieving nearly 95 percent accuracy. In addition, researchers had the algorithm sort new images from 189 slides without human intervention, which achieved more than 93 percent accuracy in all three bacteria categories. “We view this as a first step as a proof of principle,” says Kirby, who believes that in the future with further development and training the AI-powered platform could be used as fully automated bacteria classification system, “conceivably reducing technologist read time from minutes to seconds.” Time is of the essence for clinical microbiologists, he notes, as rapid identification and delivery of antibiotic medications is the key to treating bloodstream infections, which kill as many as 40 percent of patients who develop them. “You have the power of the machine’s intelligence and the power of the microbiologist together to render a diagnosis,” Kirby concludes. “I work at a big teaching hospital, but there are many smaller sites that don’t have local expertise. Slides could be scanned at these remote sites and then analyzed potentially at a central site to suggest what the diagnosis might be.” Besides clinical applications, the AI-based system could also be utilized for microbiology training and research as a “living data repository,” he adds.
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In data communications it is often required that secure communications be provided between users of network stations (also referred to as "network nodes") at different physical locations. Secure communications must potentially extend over public networks as well as through secure private networks. Secure private networks are protected by "firewalls", which separate the private network from a public network. Firewalls ordinarily provide some combination of packet filtering, circuit gateway, and application gateway technology, insulating the private network from unwanted communications with the public network. One approach to providing secure communications is to form a virtual private network. In a virtual private network, secure communications are provided by encapsulating and encrypting messages. Encapsulated messaging in general is referred to as "tunneling". Tunnels using encryption may provide protected communications between users separated by a public network, or among a subset of users of a private network. Encryption may for example be performed using an encryption algorithm using one or more encryption "keys". When an encryption key is used, the value of the key determines how the data is encrypted and decrypted. When a public-key encryption system is used, a key pair is associated with each communicating entity. The key pair consists of an encryption key and a decryption key. The two keys are formed such that it is unfeasible to generate one key from the other. Each entity makes its encryption key public, while keeping its decryption key secret. When sending a message to node A, for example, the transmitting entity uses the public key of node A to encrypt the message, and then the message can only be decrypted by node A using node A's private key. In a symmetric key encryption system a single key is used as the basis for both encryption and decryption. An encryption key in a symmetric key encryption system is sometimes referred to as a "shared" key. For example, a pair of communicating nodes A and B could communicate securely as follows: a first shared key is used to encrypt data sent from node A to node B, while a second shared key is to be used to encrypt data sent from node B to node A. In such a system, the two shared keys must be known by both node A and node B. More examples of encryption algorithms and keyed encryption are disclosed in many textbooks, for example "Applied Cryptography--Protocols, Algorithms, and Source Code in C", by Bruce Schneier, published by John Wiley and Sons, New York, N.Y. copyright 1994. Information regarding what encryption key or keys are to be used, and how they are to be used to encrypt data for a given secure communications session is referred to as "key exchange material". Key exchange material may for example determine what keys are used and a time duration for which each key is valid. Key exchange material for a pair of communicating stations must be known by both stations before encrypted data can be exchanged in a secure communications session. How key exchange material is made known to the communicating stations for a given secure communications session is referred to as "session key establishment". A tunnel may be implemented using a virtual or "pseudo" network adapter that appears to the communications protocol stack as a physical device and which provides a virtual private network. A pseudo network adapter must have the capability to receive packets from the communications protocol stack, and to pass received packets back through the protocol stack either to a user or to be transmitted. A tunnel endpoint is the point at which any encryption/decryption and encapsulation/decapsulation provided by a tunnel is performed. In existing systems, the tunnel end points are pre-determined network layer addresses. The source network layer address in a received message is used to determine the "credentials" of an entity requesting establishment of a tunnel connection. For example, a tunnel server uses the source network layer address to determine whether a requested tunnel connection is authorized. The source network layer address is also used to determine which cryptographic key or keys to use to decrypt received messages. Existing tunneling technology is typically performed by encapsulating encrypted network layer packets (also referred to as "frames") at the network layer. Such systems provide "network layer within network layer" encapsulation of encrypted messages. Tunnels in existing systems are typically between firewall nodes which have statically allocated IP addresses. In such existing systems, the statically allocated IP address of the firewall is the address of a tunnel end point within the firewall. Existing systems fail to provide a tunnel which can perform authorization based for an entity which must dynamically allocate its network layer address. This is especially problematic for a user wishing to establish a tunnel in a mobile computing environment, and who requests a dynamically allocated IP address from an Internet Service Provider (ISP). Because existing virtual private networks are based on network layer within network layer encapsulation, they are generally only capable of providing connection-less datagram type services. Because datagram type services do not guarantee delivery of packets, existing tunnels can only easily employ encryption methods over the data contained within each transmitted packet. Encryption based on the contents of multiple packets is desirable, such as cipher block chaining or stream ciphering over multiple packets. For example, encrypted data would advantageously be formed based not only on the contents of the present packet data being encrypted, but also based on some attribute of the connection or session history between the communicating stations. Examples of encryption algorithms and keyed encryption are disclosed in many textbooks, for example "Applied Cryptography--Protocols, Algorithms, and Source Code in C", by Bruce Schneier, published by John Wiley and Sons, New York, N.Y. copyright 1994. Thus there is required a new pseudo network adapter providing a virtual private network having a dynamically determined end point to support a user in a mobile computing environment. The new pseudo network adapter should appear to the communications protocol stack of the node as an interface to an actual physical device. The new pseudo network adapter should support guaranteed, in-order delivery of frames over a tunnel to conveniently support cipher block chaining mode or stream cipher encryption over multiple packets.
4.09375
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Laminitis Possibly the most feared of equine disorders, laminitis is recognised in two basic forms that we will describe as “impact” and “toxic”. Laminitis is the inflammation of the “laminæ” that bind the hoof capsule to the coffin bone. In mild cases it is just painful; in severe cases the capsule detaches from the coffin bone and rotates around the bone – often incorrectly described as “coffin bone rotation”. Laminitis can affect just the front hooves; it is usually more acute and/or severe forms that affect the rear hooves as well. Laminitis very rarely affects just the rear hooves. Defining laminitis Impact laminitis is as a result of overexposure to high impacts of the hoof and is essentially severe bruising resulting in inflammation. Toxic laminitis, is in most cases a “luxury” illness; in general confined to horses that are considered “well looked after”, this form of laminitis all to frequently results from confinement and an unsuitable diet. In a few cases, it is the result of the horse being unintentionally exposed to an unsuitable diet (for example, the horse that escapes its field and ransacks the neighbour’s supply of chicken feed!). Medicines can also trigger laminitis, the best known being certain anti-inflammatories (NSAIDs), often given in order to prevent laminitis. It should be noted that usually it is not the NSAID alone that is the cause but rather the combination with confinement that is often prescribed concurrently. Another trigger can be pregnancy and birth. A mare in foal has a raised chance of developing laminitis due to the “foreign body” that she is carrying and its inherent toxins. If, after the birth, the placenta is not fully ejected, this too can cause a laminitic reaction. As with most other forms of toxic laminitis, the mare in foal is most at risk when confined and exposed to an unsuitable diet; on the other hand, the incomplete ejection of the placenta is a risk associated with birth. Finally, PPID (Pituitary Pars Intermedia Dysfunction, formerly known as Cushing’s Disease) can also play a role in toxic laminitis; the horse becomes insulin resistant resulting in similar symptoms to the “sugar overload” seen in horses on an unsuitable diet. It is hypothetically probably that PPID falls into the category of “luxury illnesses”. The cause of PPID is quite probably dietary and is little more than an irreversible sugar overload later in life. Defining definitions There is often misunderstanding when describing the onset and severity of laminitis. There are three words that seem to cause a lot of confusion:Acute : this simply describes the rapid onset of an illness (often within hours) and is no indication of severity.Chronic : again, a time reference, chronic describes something long term or repetitive and is also not indicative of severity.Severe : what it says on the packet…but not connected with the rapidity of onset nor length of illness. The opposite of severe is mild. Identification Laminitis can be difficult to indentify initially. If the onset is not acute, the horse may initially appear to be just slightly lame; however, this lameness will affect both hooves – rarely is lameness on just one side an indication of laminitis. This lameness will get progressively worse and the horse will start to adopt a stationary pose that avoids putting any pressure on the front feet. Treatment Laminitis is not easy to treat which is probably the reason why in the past so many horses were put down fairly soon after diagnosis. Even today, many horses are put down on the advice of the vet because the condition does not appear to be improving, or even at times, appears to worsen. Even when caught early, laminitis can be very destructive of the hoof structures; clearly prevention is vastly preferable to cure. But it can be treated; but not in the way most veterinary specialists would propose these days. There is a very strong urge to confine the horse to a box, to restrict its movement, and to apply either egg-bar or inverted/reversed shoes to alleviate the effects of “coffin bone rotation”. Since the horse is likely to be in too much discomfort for it to want to move any distance, confinement is both pointless and counterproductive. By isolating a horse in discomfort, one is adding to its problems psychologically. In addition, by confining the horse to a stable, its hooves are subjected to a degenerative environment of excreta and should perforation of the sole happen, this is most certainly the last place the horse should be. Furthermore, the toxins causing the inflammation that are now present in the hoof need to be flushed which can only happen with good circulation; confining the horse severely restricts circulation. The application of any sort of shoe displays a complete ignorance of the hoof, its mechanism and its function. Even for those practitioners who consider the coffin bone to be suspended inside the hoof capsule, it should be plainly obvious that the laminitic hoof, where the hoof capsule and the coffin bone are becoming separated, cannot in any way support the weight of the horse. And yet these people insist on applying “orthopædic” horseshoes (a nonsense term worthy of Lewis Carroll). Thus, it should be clear that the initial way to proceed is to remove horseshoes, if they are present, and to turn the horse out. However, it must be noted that the horse should not be turned out to rich pasture; if there is a high sugar content in the grass, then this will probably continue to affect to hoof and exacerbate the problem. Short, well cropped grass is a more viable alternative which ensures the horse has food but is encouraged to move to find it. Both movement and the small amount of food will be advantageous to the horse. Do not restrict the horse’s diet and do not feed commercial feed. Only grasses and hay. Ensure that the hooves are trimmed such that the caudal structures (the “heels”) are lowered to a minimum – this is best done over a number of days rather than in one fell swoop – and the hoof wall is not carrying the weight of the horse. The latter is one of the major bones of contention with the traditional veterinary/farriery world; the hoof wall is not a weight bearing structure even in the healthy hoof so loading it when the hoof is unhealthy, and particularly when its connection with the underlying coffin bone is so weakened, is only going to worsen matters. The horse must be kept under semi-permanent supervision to ensure it gets enough movement and the hooves must be trimmed frequently (as often as possible) to keep ahead of the damaging effects of the inflammation. Recovery This can be long and slow. Even with horses that have been caught in the early onset of laminitis, sufficient damage can have been done to complicate the healing process. In simple terms, the hoof wall must regrow to follow the line of the coffin bone (the hoof wall cannot “reattach” to the coffin bone, only new growth is attached). Generally this process takes up to a year (the length of time needed to grow a complete new hoof) but, depending upon the severity of the laminitic attack, it can be complicated by the formation of abscesses and by the rebuilding of the internal structures of the hoof which in turn can lead to deformations particularly of the sole. It is a process that can take more than two years before any real signs of recovery are evident. Prevention Obviously prevention is not so easily applicable to accidents – the horse escaping and devouring next-door’s grain store springs to mind. But in almost all other situations, it is quite possible to avoid – even impact laminitis. A shod hoof cannot absorb impact with the ground in the way that is intended and this can cause concussive impact damage. Asking an unshod horse to gallop over a stony or rocky path will similarly subject the hoof to abnormal stresses. The answer here is obviously never to shoe a horse and never ask the horse to do something it would not normally do. Confinement in a stable reduces the horse’s movement and so also its use of sugars ingested. The majority of stabled horses are also fed a completly unsuitable diet – commercial feed with grain, cereals, molasses and other starches and sugars. This creates a sugar overload. In early spring these horses, that have often been kept confined for the whole of the winter, are turned out to sugar rich pastures – pushing the sugar overload over the top… The answer here is firstly that horses should never be confined to stables – not even for a part of the day; secondly they should not be fed anything other than grasses and, at times of shortage, hay; thirdly, rye grasses and other high-production grasses should be avoided – these are particularly intended for cattle to increase both milk and meat production at the cost of their general health (laminitis is well known among cattle too); fourthly, horses should not be overfed during the winter months. This last point is always highly controvertial among horse owners; the general equine population, like its human counterpart, is overweight and for some reason, we seem to “prefer” our horses to be overweight. Most people, including animal welfare organizations, don’t know at what point a horse becomes overweight – the two body score indices in use, the various five-point scales and the Henneke nine-point scale both put the healthy horse too far up the scale! The reason for not overfeeding in winter is quite simple and very natural. This is how the horse has evolved and by reducing food intake during the winter, the insulin resistance cycle is broken. This cycle involves ingestion of sugars during the growing months whereby the sugar levels in the body increase; with the onset of winter, the amount of sugar ingested is significantly reduced allowing the body to “reset” and start all over again the following spring. The horse that continues to eat at the same rate during the winter does not get this essential reset and so, in the spring, the increased sugars just go piling on top of an already overloaded system. Feeding commercial foods – at any time during the year – just adds yet more to the overload. Correct treatment of suspected laminitis will also go toward prevention; avoiding administration of NSAIDs, application of horseshoes or confinement are three very important factors sadly ignored by the mainstream veterinary profession. The mare in foal should, as with any other horse, never be confined to a stable. She should be allowed to roam in as large a space as possible with her companion horses and not isolated as if she was ill. This in itself will be sufficient to greatly lower the chance of laminitis but to eliminate it more or less completely, the mare should not be fed commercial feed, just grasses and, when grasses are scarce, hay. She does not need feeding up with anything unnatural. The incalculable risk moment for the mare in foal is post partum – when in fact, she is no longer in foal; if the placenta is not fully ejected this can cause a toxic reaction; it is therefore essential to check that the placenta is complete after the foal is born and if at all in doubt, call your vet out.
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Health Library Health Resources Health Encyclopedia A Child's Concept of Death For infants and toddlers, death has very little meaning. School-aged children begin to understand death as permanent, universal, and inevitable. A predominant theme in adolescence is a feeling of immortality or being exempt from death. Discussing Death with Children The ultimate goal in discussing death with a dying child is to optimize his or her comfort and alleviate any fears. If the child is not ready to discuss death, the most helpful step parents can take is to wait until he or she is ready. Anticipatory Grief Anticipatory grief is similar to the normal process of mourning, but it occurs before the actual death. The Dying Process Understanding the physical and mental changes the body goes through as death occurs, may help alleviate some fears and misconceptions about death. Grief and Bereavement The process of grieving is often long and painful for parents, siblings, relatives, friends, peers, teachers, neighbors, and anyone that understands the loss of a child. Physical Needs of the Dying Child A terminally ill child has many of the same needs as any seriously ill child, including a routine for sleep and rest, and for pain management. For Parents: Important Decisions to Be Made in the Dying Process Detailed information on important decisions to be made when a child is dying, including the right to refuse treatment, to die at home versus the hospital, advanced directives, do not resuscitate, autopsy, organ donation, palliative hospice care, and funeral arrangements.
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It should appear to us clearly by now that inheritance is useful by allowing us to use an object that was already created but "upgrade" it with new features that were not available when the original object was born. In most cases, when creating a class, you may not thing that other classes would be inherited from it. In fact, this will usually not be your concern: you simply create a class and use it as needed. In some other cases, rather as you build your experience with Visual Basic. You may create a class that, although useful at the time, you may already think of other classes that would be based on it. This means that, at the time you are creating such a class, you would already keep inheritance in mind. Visual Basic provides various features that can assist you with creating and implementing class with different goals in mind. Abstracting a Class Imagine that, when creating a class, you already find that it is too or highly generalized to serve one particular purpose. As an example, imagine you start creating a class you intend to use to process calculations for a rectangle, or a square, or a parallelogram, or even a triangle: Rectangle Square Parallelogram Triangle You start thinking that the same class could be used for different types of geometric shapes. In this case, instead of creating a different class for each shape, you can create a generalized class that these shapes can be based on. Unfortunately, these shapes, although each characterized as geometric, don't have much in common; otherwise they would not be different. One of their common characteristics is that each has a name. While the parallelogram and the triangle have a base, the rectangle and the square don't explicitly have one. Also, neither the perimeter nor the area of these shapes are calculated the same. Still, as long as you find at least one characteristic that these objects have, you can create a class that would share. In other words, you can create a class that features one or more characteristics that these objects have. Then each object would customize its behavior(s) based on its particular characteristics. This is the basis of abstraction. A class is referred to as abstract when it is only used to lay a foundation for other classes. In the Microsoft Visual Basic language, to create an abstract class, you must precede its Class keyword with MustInherit. Here is an example: File: Quadrilateral.vb Public MustInherit Class Quadrilateral End Class After creating a class and marking it as MustInherit, you can add one or more members to it, as done in the previous examples we used so far. Here is an example: File: Quadrilateral.vb Public MustInherit Class Quadrilateral Public Function ShowDescription() As String Return "Geometric Shape" End Function End Class If you create a class and mark it as MustInherit, it is considered incomplete. Because of that, although you can declare a variable of that type, you cannot initialize its instance using the New operator. Consider the following example: File: Exercise.vb This would produce an error because you cannot use New to instantiate a MustInherit class. This means that, before using a MustInherit class, you must derive a class from it. Overriding Members of an Abstract Class The main idea for creating a MustInherit class is to lay a foundation that other classes can exploit. When creating the members of such a class, you can prepare them to be overridden. You have the option of creating overridable and non-overridable members. You will make the decision based on your requirements. Sometimes when creating a particular member, you may intend all derived classes to implement their own version of the member. You must clearly indicate that any class that wants to inherit from the MustInherit class must (also) override a particular member. Such a member must be marked with the MustOverride keyword. To do this, when creating the member, precede its type with the MustOverride keyword. Here is an example: File: Quadrilateral.vb Public MustInherit Class Quadrilateral Public MustOverride Property Area() As Double End Class In the same way, you can add as many members as necessary. You will mark as MustOverride those of your choice and you can create others without MustOverride. Here are examples: File: Quadrilateral.vb Public MustInherit Class Quadrilateral Public Function ShowDescription() As String Return "Geometric Shape" End Function Public MustOverride Property Area() As Double End Class After creating a MustInherit class, you can inherit new classes from it using the Inherits keyword we saw in the previous lessons. Here is an example: Public Class Square Inherits Quadrilateral End Class When deriving a class from a MustInherit, the first rule you must observe is that each member of the abstract that was marked as MustOverride must be overridden. Based on this, in our Square class, you must (at least) implement the Area property. Here is an example: File: Quadrilateral.vb Public MustInherit Class Quadrilateral Public Function ShowDescription() As String Return "Geometric Shape" End Function Public MustOverride ReadOnly Property Area() As Double End Class Public Class Square Inherits Quadrilateral Public Overrides ReadOnly Property Area() As Double Get Return 0 End Get End Property End Class In the derived class, as a new one, you can add new members as you judge them necessary. Here are examples: File: Quadrilateral.vb Public MustInherit Class Quadrilateral Public Function ShowDescription() As String Return "Geometric Shape" End Function Public MustOverride ReadOnly Property Area() As Double End Class Public Class Square Inherits Quadrilateral Public sd As Double Public Sub New() sd = 0 End Sub Public Sub New(ByVal side As Double) sd = side End Sub Public Property Side() As Double Get Return sd End Get Set(ByVal Value As Double) If Value <= 0 Then sd = 0 Else sd = Value End If End Set End Property Public Overrides ReadOnly Property Area() As Double Get Return sd * sd End Get End Property End Class After deriving a new class from a MustInherit class, you can declare a variable of it and instantiate it using the New operator. Here is an example: These declaration and instantiation are legal but the (tri) variable gives you access only to members that are present in the parent class. This means that this declaration gives you access to the ShowDescription() method and the Area property of the Quadrilateral class. This is illustrated in the following: When instantiating a class derived from a MustInherit class, if you want to access its members, you must apply its name to the New operator as we saw in the last example of the previous section. Here is an example: In Lesson 5, we saw that a procedure was an assignment that complemented a program. We also saw that there were two types of procedures: functions and sub routines. These concepts of sub procedures and functions also apply to classes. This means that a procedure that process a class, it can be passed a class as argument, and it can return a class. As described in Lesson 8, to create a sub procedure, type the Sub keyword followed by a name, followed by parentheses and an end of line. To indicate the end of a sub procedure, you must type End Sub. Therefore, the syntax of a sub procedure is: SubProcedureName() End Sub Between the Sub and the End Sub lines, you can declare the necessary variables and they can be of regular types or based on classes. Here is an example: In the same way, you can declare as many class variables as you see fit in a procedure. Returning an Object So far, as we have learned since Lesson, we know that a function can be used to return a value. In the same way, you can create a function that returns an object of a class. When creating such a function, set its type as that of the class it would return. The formula to follow is still: FunctionFunctionName() AsClassNameEnd Function In the body of the class, which is the section between the Function and the End Function lines, you can perform any assignment you judge necessary. For example you can declare local variables. Before exiting the function, you must make sure it returns a value based on its As type. You can do this using the Return keyword followed by the value to return. Here is an example: Like a regular variable, a class can be passed as argument to a procedure. When a procedure receives such an argument, it can process it as necessary. All the rules we reviewed for regular variables apply to a class, as long as you keep in mind that an object has members that you may need to be aware of. When calling the procedure, make sure you pass it a value argument based on the class it passed to it. Here is an example of a class passed as argument: Besides the function, in Lesson 5, we saw that, by passing an argument by reference, a sub procedure could return a value. This characteristic also applies to a class passed as argument. When passing the argument, precede it with the ByRef keyword. In the procedure, process the argument as you see fit, unless you choose not to. When calling the procedure, pass it a valid variable based on the type of the argument. Here is an example: Like a regular variable, a class can be locally declared as static, using the Static keyword. If the value of such a locally declared variable changes, when the procedure ends, the value of the variable is changed and would be kept until the next call. Optional Arguments When passing an argument of a class, you can specify that it is not required. Such an argument is considered optional. To specify that an argument is optional, when creating its procedure, type the Optional keyword to the left of the argument's name and assign it the default value. All the other rules we reviewed for optional arguments are also applied here. Procedure Overloading If you want to create various procedures that takes a class argument, you can create a procedure with the same name but different signatures. This is referred to as overloading the procedure. When doing this, follow the same rules we reviewed for overloading a procedure: the must have the same name, they cannot have the same number of argument when the arguments at each position are of the same types. Sealed Classes Introduction All of the classes we have used so far can serve as parents of other classes. This is the default behavior of a regular class: the ability to derive a new class from it. In some cases, you may not want any class to be derived from a particular class you are creating. Such a class is referred to as sealed. A class is said to be sealed when you cannot inherit from it. If you try, you would receive an error. To create a sealed class in Microsoft Visual Basic, precede the name of the class with the NotInheritable keyword.
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As an image display device increasingly develops, people have higher requirements for high-quality and high definition image information. In practice, a digital image is usually affected by an imaging device, noise interference in an external environment, and the like, during processes of digitalization and transmission. Therefore, such a digital image with noise interference is usually referred to as an image with noise or a noisy image. Noise may reduce a resolution of a digital image and affects display details of the image, which is extremely disadvantageous to subsequent processing of the image. Therefore, effective noise suppression is essential to an image application. Image noise reduction is of great significance in a video processing system. In a television system, deinterlacing, anti-aliasing, and image scaling require that the system provide an image without noise or with low noise as input image information. In a surveillance system, image noise reduction is also a main method for improving quality of a surveillance image. TNR is an important technical method for image noise reduction. A TNR method that is commonly used in the prior art can be implemented in the following manner:pixeltnr(x,y,t)=pixeltnr(x,y,t+Δt)×alpha+pixel(x,y,t)×(1−alpha)where pixel indicates an original noisy image, pixeltnr is an image obtained after TNR, and in a digital image, the foregoing variables are both replaced with discrete variables, x and y are two-dimensional space coordinates, and t is a one-dimensional time coordinate, where x and y determine a position of an indicated pixel, and t represents a position of a current image in an image sequence, that is, a quantity of frames, Δt is a time offset, and Δt is usually set to 1, alphaε[0,1], and alpha is a blending coefficient and is used to determine a noise reduction intensity, a larger alpha indicates a higher noise reduction intensity, and vice versa. The TNR in the prior art is mainly TNR based on determining of movement/still. A movement level of corresponding image content is determined according to a size of a frame difference, and a corresponding blending coefficient is selected according to the movement level. When the frame difference is lower, it is considered that a corresponding movement level is lower, a movement is tending to be still, and a higher blending coefficient alpha is selected, and vice versa. During a process of implementing the present disclosure, the inventors of the present disclosure found that in the TNR based on determining of movement/still, only a frame difference is used as a basis for determining whether an image moves, and a corresponding blending coefficient is selected according to a result of the determining. However, a detection error may easily occur if only a frame difference is used as a basis for determining a movement of an image. If a moving image is determined to be a still image, smearing of the image may occur, and details of the image may be lost. If a still image is determined to be a moving image, a noise reduction effect may be poor for an image with large noise. Therefore, the TNR based on determining of movement/still cannot adapt to different noise scenarios.
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Would children be adequately protected by existing intervention levels during a radionuclear emergency? The question arises as to whether radiation standards and guidelines set for adults are sufficiently protective of children. To answer this question, published literature values have been used to calculate radiation doses to children and adults from external and internal exposure to a suite of 30 radionuclides commonly found in the environment. It was found that older children and adults face about the same degree of risk from external radiation exposures, although doses may be ∼30 % elevated for infants due to their smaller body size. Inhalation risks in children are to a large degree offset by lower breathing rates and it is only in the case of iodine isotopes that children are more at risk. Ingestion of contaminated food products is more complex. Isotopes of iodine and the bone-seeking elements strontium and radium can give radiation doses up to an order of magnitude higher than for adults.
3.390625
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Q: The union, intersection and complement of events On the Probability chapter of a 1995 mathematical statistical book I am reviewing I have found the following exercise: Let A and B be arbitrary events. Let C be the event that either A occurs or B occurs, but not both. Express C in terms of A and B using any of the basic operations of union, intersection and complement. Now, the book suggested answer is to describe the entire sample space as: $$\Omega=(A\cap B)^{C}\cap(A\cup B)$$ I think the correct answer is: $$\Omega=(A\cap B)^{C}\cup(A\cap B)$$ and $$C=(A\cap B)^{C}$$ Where is the error that I have made? A: $C$ (the symmetric difference of $A$ and $B$) is obtained by overlaying (intersecting) $A\cup B$ and $(A\cap B)^c$, whence $C = (A\cup B) \cap (A\cap B)^c$: Another expression frequently used is $C = (A\cap B^c) \cup (B\cap A^c)$. The left-hand term is the pure red lune in the figure while the right-hand term is the pure blue lune; together, they form $C$. A: Actually, you both got it wrong! You're right in thinking that $$\Omega=(A\cap B)^{C}\cup(A\cap B)$$ since it is true that, for any set $D$ in $\Omega$, $D^C \cup D=\Omega$. However, $C$ is the part of $A\cup B$ such that only one of $A$ and $B$ occurs. In other words, you need both the event $(A\cup B)$ and the event $(A\cap B)^{C}$ to occur. Thus $$C=(A\cap B)^{C}\cap(A\cup B)$$ which is what the book claimed was $\Omega$.
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The placenta and intrauterine programming. Intrauterine programming is the process by which the structure and function of tissues are altered permanently by insults acting during early development. In mammals, the placenta controls intrauterine development by supplying oxygen and nutrients, and by regulating the bioavailability of specific hormones involved in foetal growth and development. Consequently, the placenta is likely to have a key role in mediating the programming effects of suboptimal conditions during development. This review examines placental phenotype in different environmental conditions and places particular emphasis on regulation of placental nutrient transfer capacity and endocrine function by insults known to cause intrauterine programming. More specifically, it examines the effects of a range of environmental challenges on the size, morphology, blood flow and transporter abundance of the placenta and on its rate of consumption and production of nutrients. In addition, it considers the role of hormone synthesis and metabolism by the placenta in matching intrauterine development to the prevailing environmental conditions. The adaptive responses that the placenta can make to compensate for suboptimal conditions in utero are also assessed in relation to the strategies adopted to maximise foetal growth and viability at birth. Environmentally-induced changes in placental phenotype may provide a mechanism for transmitting the memory of early events to the foetus later in gestation, which leads to intrauterine programming of tissue development long after the original insult.
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Typhoid Fever Last Reviewed: November 2011 What is typhoid fever? Typhoid fever is a bacterial infection of the intestinal tract and occasionally the bloodstream. It is an uncommon disease with only a handful of cases occurring in New York each year. Most of the cases are acquired during foreign travel to underdeveloped countries. Typhoid fever is caused by Salmonella Typhi (S. Typhi), a strain of bacteria that lives only in humans. Who gets typhoid fever? Anyone can get typhoid fever but the greatest risk exists to travelers visiting countries where the disease is common. Occasionally, local cases can be traced to exposure to a person who is a chronic carrier. Outbreaks are rare. How is the germ spread? Typhoid germs are passed in the feces and, to some extent, the urine of infected people. The germs are spread by eating or drinking water or foods contaminated by feces from the infected individual. What are the symptoms? Symptoms may be mild or severe and may include fever, headache, constipation or diarrhea, rose-colored spots on the trunk and an enlarged spleen and liver. Relapses are common. Fatalities are less than 1 percent with antibiotic treatment. How soon do symptoms appear? Symptoms generally appear one to three weeks after exposure. For how long can an infected person carry the typhoid germ? About 5 percent of people infected with S. Typhi become lifelong carriers, releasing the germ in their stool for years, which can spread the disease. How is typhoid treated? Specific antibiotics such as ampicillin, trimethoprim-sulfamethoxazole and ciprofloxacin are often used to treat cases of typhoid. Should infected people be isolated? Because the germ is passed in the feces of infected people, only people with active diarrhea who are unable to control their bowel habits (infants, certain handicapped individuals) should be isolated. Most infected people may return to work or school when they have recovered, provided that they carefully wash hands after toilet visits. Children in daycare and health care workers must obtain the approval of the local or state health department before returning to their routine activities. Food handlers may not return to work until three consecutive negative stool cultures are confirmed. Is there a vaccine for typhoid? Yes. A vaccine is available for people traveling to underdeveloped countries where significant exposure may occur. As important, pay strict attention to food and water precautions while traveling to countries where typhoid is common. For more information about vaccination, speak to your health care provider.
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General Tips on Playing With Both Hands 1. Learn the piece, example, etc hands separate first, then put hands together. 2. Play SLOWLY 3. When first learning to play hands together, avoid examples with complicated rhythms. 1. Scales Scales are a good way for beginners to develop dexterity and coordination when playing keyboard with both hands. This is because playing scales involves playing notes in synch with one another. Usually scales are played with the same rhythm in both hands, so no worries trying to play different rhythms and concentrating on notes at the same time. Where should you start? Start with the C Major scale and learn it hands separate. Then try playing the scale ascending very slowly with both hands. Once you are able to play the scale ascending, learn the scale descending. Then play the scale ascending and descending. Learn 1 scale a week until you can play all the major scales slowly. Then gradually increase the tempo over weeks to achieve greater speed. Here is a scale exercise. Start with C Major and play up the scale with half notes in the right hand while playing whole notes in the left hand. Then do the same but with half notes in the left hand and whole notes in the right had. 2. Hanon Are great for developing two handed dexterity between both hands. These are for playing in parallel meaning you are playing the same intervals at the same time. Try learning one a day or one a week until you learn them all. Play them slow at first then over weeks gradually increase the tempo. http://www.hanon-online.com/ 3. Czerny These are highly recommended for practice playing different rhythms and pitches for each hand. http://pianoexercises.org/exercises/czerny/
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Several techniques are known in the semiconductor industry for providing isolation between transistors. One such method employs an anisotropic etch of a silicon crystal having a &lt;100&gt; orientation. The etched surface is oxidized and deposited with a thick layer of polysilicon to form islands of single crystal silicon. Subsequently, the wafer is inverted, polished and etched back to expose the silicon islands in which the transistors are formed. Problems associated with this technology are grind and etch-back non-uniformity, limited wafer diameter, large device size, device size dependence on isolation depths, and high parasitic AC impedance with polysilicon substrates. Several other methods exist for transistor isolation. However, these approaches include PN junction isolation and Local Oxidation of Silicon ("LOCOS") isolation. As these isolation methods are designed for bulk silicon material, they are all subject to parasitic interaction with the substrate. Still a further method for providing dielectric isolation uses a trench implementation filled with a dielectric material. In FIG. 1 of U.S. Pat. No. 4,631,803, a known trench structure is shown. The trench structure illustrated is intended to minimize stress at the interface between the trench and the semiconductor substrate by curving the bottom of the trench. Moreover, in FIGS. 2 and 3 of U.S. Pat. No. 4,631,803, a trench structure is illustrated. Here, the inventor teaches the formation of a trench directly on a semiconductor substrate. The trench is filled with a silicon dioxide layer 38, followed by a first silicon nitride layer 40, followed by a refill 42 of either undoped polysilicon or silicon oxide. In FIG. 3, a second silicon nitride layer 48 is also employed. There are several disadvantages to the trench structure of disclosed and illustrated in FIGS. 2 and 3 of U.S. Pat. No. 4,631,803. Firstly, silicon nitride is a brittle film with a high value of intrinsic stress. Further, silicon nitride has a different rate of thermal expansion than silicon, silicon dioxide, as well as polysilicon. As such, the trench arrangement of FIGS. 2 and 3 is prone to defects and generations of dislocations in silicon due to the stress associated with the silicon nitride layer(s). Moreover, silicon nitride has a higher dielectric constant in comparison with silicon dioxide. Given the potential for parasitic capacitance by the formation of the trench structure, a higher resultant parasitic capacitance value is created. Furthermore, the teachings of the trench arrangement of FIGS. 2 and 3 also fail to provide a radiation hardened trench substantially immune to flicker noise. This is because the trench structures of FIGS. 1, 2 and 3 are contained in a bulk silicon semiconductor substrate. This allows for PN junction latch-up problems with the substrate under harsh environments, such as, for example, high voltage, high temperature and radiation environments. In light of the limitations of these known isolation trench designs, a need exists for an isolation trench which is radiation hardened and substantially immune to flicker noise. Further, the semiconductor industry requires an isolation trench which minimizes stress and defect generation in silicon. Further, an isolation trench on an SOI substrate is needed to provide a means for intrinsic gettering on a semiconductor substrate. Complete dielectric isolation is also in demand to minimize noise and latch-up effects under harsh environments. Furthermore, an isolation trench is required which has improved stress related characteristics, and substantially reduced dislocation generation. Additionally, there is a need in the semiconductor industry for an isolation trench having a substantially lower parasitic capacitance and resistance.
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Electric motors are used almost everywhere in society to produce different mechanical movements, for example, rotating pumps and fans. There are numerous different types of electric motors, of which the most common is the so-called squirrel-cage motor. The connection of a squirrel-cage motor to the network is known to cause a substantial switching current surge; the current taken from the network when starting can transiently be over 6 times the rated current. This kind of current surge often causes problems, such as the need to dimension the fuses and cables of the supply circuit to be larger than the load during actual operation would require, as well as the extra costs incurred by this kind of over-dimensioning. Generally the larger the power output of the motor is in question, the larger problem the switching current surge is. One prior-art solution for reducing the starting current is to use a so-called soft starter, which may include a circuit implemented with thyristors, with its control unit, and in which the control angle of the thyristors is controlled so that the voltage of the motor decreases to avoid the over large current of the starting phase. This type of solution is known, for example from publications DE4406794 and U.S. Pat. No. 5,859,514. A drawback of the solution is the cost of starting and the power loss during operation as the motor current runs continuously through it. In order to reduce continuous power loss, the prior art solution bypass the soft starter by connecting the motor directly to the network after the starting phase with a shunt contactor. The use of a frequency converter for starting the motor without a switching current surge is also a well-known solution. When the load requires a varying speed of rotation, the use of a frequency converter is otherwise a natural solution. If, however, the load of the motor allows continuous operation at a fixed frequency of the supply network, the prior art solutions use a shunt circuit implemented with contactors to minimize power losses, with which shunt circuit the motor is disconnected after the starting phase from the frequency converter and connected directly to the network. A shunt circuit may be used in the prior-art pump automatics according to FIG. 2a, in which one frequency converter and a number of motors of which each can be connected either to the frequency converter, or directly to the network. With the solution the total flow produced by the pumps can be steplessly adjusted from zero up to maximum delivery, in which case all the motors operate at their rated speed. Also a motor accelerated to its rated speed with a frequency converter can take a substantial connection current surge, even greater than the starting situation, when it is connected directly to the network. This occurs if the amplitude and phase angle of the so-called residual voltage evident in the connectors of the motor after disconnecting from the frequency converter differ from the amplitude and phase angle of the supply network at the time when the motor is connected directly to the network. Owing to the deceleration of a loaded motor and the switching delays of the contactors, which can be in the range 40 . . . 100 ms, a simple and reasonably priced prior-art method or arrangement to synchronize the residual voltage and the voltage of the supply network at the time of connection is not found.
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Map Viewer The active fire map is a service offered and produced by NASA from data collected by satellites. The information collected is treated very quickly and made available to the public in a few hours. With all this we can know in a rather objective way the approximate place where a point of fire has occurred and the magnitude of it. - Topographic maps of Belgium offered by the Institut géographique national (IGN) at different scales (Between 1:4,000,000 and 1:2,500) - Map of the open Street Map collaborative project where users themselves map the world - Aerial photographs of Belgiumdel - CADastral mapping of SPF Finances - Open Street Map (OSM) - Traces made by users of the Strava app
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In situ measurements of shear stresses of a flushing wave in a circular sewer using ultrasound. Deposits build up in sewer networks during both spells of dry weather and in connection with storm water events. In order to reduce the negative effects of deposit on the environment, different cleaning technologies and strategies are applied to remove the deposits. Jet cleaning represents the most widely used method to clean sewers. Another alternative cleaning procedure is flushing. On account of new developments in measurement and control panels, the flushing method is becoming more important. Therefore, in the last few years a number of new flushing devices have been constructed for application in basins, main sewers and initial reaches. Today, automatic flushing gates are able to accomplish cleaning procedures under economical and ecological conditions. The properties of flushing waves for cleaning sewers have been determined by several mathematical-numerical studies. These various investigations use altering numerical schemes, are based on different sets of physical equations and take one- or more dimensional aspects into account. Considering that bottom shear stress is the key value to evaluate the beginning of motion of any deposit, one may use this value that has to be determined by measurements. This paper deals with shear stresses caused by flushing waves which have been measured by an ultrasonic device that can determine the velocity in different depths of flow. Thus, it is possible, within certain limits, to calculate bottom shear stresses based on the log-wall law. Further discussion will deal with the requirements of measurements, its uncertainty and aspects in respect to the application of simulation of flushing waves.
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Q: Displaying number of alphabetical letters and the number of decimal digits in C I have been working on this simple code for hours now, and I have no idea what is wrong! I need to display number of alphabetical letters and the number of decimal digits in standard input. So far I have this: #include<stdio.h> #include<ctype.h> int isalpha(int); int isdigit (int); int main() { int c; while((c=getchar())!=EOF) printf("The number of letters is %d and the number of digits is %d.\n", isalpha(c), isdigit(c)); return 0; } int isalpha(int one) { int ch; int i; i=0; scanf("%d", &ch); if(isalpha(ch)) i++; return i; } int isdigit(int two) { int a; int k; k=0; scanf("%d", &a); if(isdigit(a)) k++; return k; } Program crashes whenever I try to run it and I have no clue what part of the code is wrong. Although I don't have much experience in this field yet, so any help is highly appreciated! Thank you in advance. A: Just use the existing API's gently and get the count as shown below int alp = 0; int dig = 0; while ((c = getchar()) != EOF) { if (isalpha(c) alp++; else if (isdigit(c)) dig++; } printf("The number of letters is %d and the number of digits is %d.\n", alp,dig); PS: Take care to flush the newline char if you have \n in the input
3.34375
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Studies demonstrating that breastfeeding protected infants from respiratory infections began in the early 20th century. At the time, it was presumed that this was a result of nutritional deficiencies in formula ([@bib1]). In the mid-20th century, it became apparent that breast milk was more than a source of calories, but also a vehicle for the transmission of antibodies, immune cells, and oligosaccharides meant for microbial, rather than infant, nutrition ([@bib2]). As a consequence, infant formulas now include substances meant to promote a healthy microbiome, yet formula-fed infants are still more susceptible to respiratory infections ([@bib3]). Despite more than a century of data on the role of breast milk in protection from respiratory infections, we still do not know whether or how maternal antibodies help shape the composition of the upper respiratory tract microbiome, whether breast milk directly promotes the growth of some respiratory microbes over others, or whether protection from respiratory infections is primarily a consequence of immune maturation. Mode of delivery also alters the oral and nasopharyngeal microbiota, and ultimately affects susceptibility to infection. Infants born by vaginal birth are quicker to acquire species such as *Corynebacterium* spp., *Moraxella* spp., and *Dolosigranulum* spp., which are associated with reduced colonization of respiratory pathogens, than their Caesarian-born counterparts ([@bib4]). How colonization of the nasopharynx by microbes that are not major components of the vaginal microbiota occurs is not clear, but may be a result of immune development as opposed to direct seeding of microbes ([@bib5]). Although the mechanisms of microbiome development are not fully elucidated, in this issue of the *Journal*, Man and colleagues (pp. [760--770](10.1164/rccm.201810-1993OC)) provide provocative evidence that both the composition of the infant microbiome and the ability to maintain the topography of the nasopharyngeal community are important for protection from respiratory infections early in life ([@bib6]). Expanding a previous study of the nasopharyngeal microbiome from birth to 6 months ([@bib7]), Man and colleagues examined the oral microbiome in the same cohort and investigated whether changes in oral and nasopharyngeal communities were associated with respiratory tract infections in early life. They previously had confirmed findings that breastfeeding and mode of birth influences these microbial communities ([@bib5], [@bib8]), and identified that the presence of certain microbes such as *Neisseria* spp. and *Prevotella* spp. in the first month of life are predictive of future respiratory infection. These data might lead one to conclude that the presence of some microbes enriched by birth mode or breastfeeding protect against infections. Indeed, this is consistent with decades of carriage studies that demonstrate that carriage of some pathobionts will protect against colonization by others ([@bib9]). The surprising element of this study is that changes in the nasopharyngeal microbiome occurred up to a month before the occurrence of a respiratory infection and were characterized by an increase in primarily oral taxa (e.g., *Neisseria lactamica*, *Prevotella nanceiensis*, *Fusobacterium* spp.) in the nasopharyngeal microbiota. It is well documented, and Man and colleagues confirm, that the nasopharyngeal microbiome changes during a respiratory infection. These changes may be a result of direct microbial competition, leukocyte recruitment and concomitant changes in the oxidative environment ([@bib10]), and/or changes in mucus production ([@bib11]). It is possible, but not proven, that the infant nasopharyngeal microbiome becomes supportive of oral species, which include many anaerobic species, before infection as a result of changes in oxidative tension resulting from subclinical inflammation or immune involvement. Limitations of the study include the fact that respiratory tract infections were confirmed by symptoms rather than definitive virologic testing. Timing of childhood vaccinations was also not recorded. The majority of the children in the study would have been vaccinated with the pneumococcal conjugate vaccine at 6--9 weeks, and again at 4 months ([@bib12]). Pneumococcal vaccination alters the composition of the respiratory tract microbiota, and could conceivably contribute to observed changes in the microbiota that precede infection ([@bib13]). In general, 16s rRNA sequencing does not provide sufficient resolution of *Streptococcus* spp. to determine whether acquisition of *S. pneumoniae* was one of the events that triggered a loss of topography. Another counterintuitive finding was the role of daycare in microbial dysbiosis. As many parents will attest, having a child enter daycare can be the start of several months of fevers and runny noses. Five of the children in the study developed respiratory tract infections in their first month of daycare, but the loss of nasopharyngeal topography was apparent a month earlier. This implies that the loss of topography may predispose children to infections once there is a second insult, such as exposure to new microbes or the stress of beginning daycare. Collectively, these data imply that the upper respiratory tract microbiome is modified by factors we do not yet understand. Despite the physiologic differences between the nasopharynx and oral cavity, the distinction between these topographies is blurred at times of immunological or possibly physiological stress. Older adults are also highly susceptible to respiratory infections and also lose topographical distinctions between the naso- and oropharynx ([@bib14]). Although the processes of immune development and immunosenescence are quite different, perhaps the end result, loss of topography preceding respiratory infections, is the same. D.M.E.B. is the Canada Research Chair in Aging & Immunity. M.G.S. is the Canada Research Chair in Interdisciplinary Microbiome Research. Research in the D.M.E.B. and M.G.S. laboratories is supported by the M.G. DeGroote Institute for Infectious Disease Research, the Farncombe Institute for Digestive Health, and the McMaster Immunology Research Centre. Originally Published in Press as DOI: [10.1164/rccm.201903-0687ED](http://dx.doi.org/10.1164/rccm.201903-0687ED) on April 12, 2019 [**[Author disclosures](http://www.atsjournals.org/doi/suppl/10.1164/rccm.201903-0687ED/suppl_file/disclosures.pdf)**]{.ul} are available with the text of this article at [www.atsjournals.org](http://www.atsjournals.org).
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Q: Why did the Old Forest respond to the hobbits? In the Fellowship of the Ring, why was the Old Forest able to respond to what the hobbits said or did? The forest is not composed of Ents, which can think, feel, and walk, yet the trees shift and change the paths and make ominous noises. Is this just a result of the hobbits imagination and fears? Some Examples: Pippin suddenly felt that he could not bear it any longer, and without warning let out a shout. 'Oi! Oi!' he cried. 'I am not going to do anything. Just let me pass through, will you!' The others halted startled; but the cry fell as if muffled by a heavy curtain. There was no echo or answer though the wood seemed to become more crowded and more watchful than before. This is right before they find the Bonfire Glade: But at that moment Merry gave a whistle of relief and pointed ahead. "Well, well!" he said. "These trees do shift. There is the Bonfire Glade in front of us (or I hope so), but the path to it seems to have moved away!" (emphasis and parenthesis not mine.) The third example is under Old Man Willow, yet another example of unexplained movements and actions by trees. Frodo and Sam are setting a fire near the tree. Apparently the tree can talk, at least to those inside it. "Do you know, Sam," (Frodo) said at length, "the beastly tree threw me in! I felt it. The big root just twisted round and tipped me in!" (emphasis not mine. Parenthesis mine.) Merry was trapped: another crack had closed about his waist; his legs lay outside, but the rest of him was inside a dark opening, the edges of which gripped like a pair of pincers. "Put it out! Put it out!" cried Merry. "He'll squeeze me in two, if you don't. He says so!" Finally, why can these trees move of their own accord? Is it some great evil being controlling them and trying to obstruct the hobbits and the Ring from reaching Rivendell? A: The relevant part from TT is given in Book 3, Chapter 4 (Treebeard): 'The trees and the Ents,' said Treebeard. 'I do not understand all that goes on myself, so I cannot explain it to you. Some of us are still true Ents, and lively enough in our fashion, but many are growing sleepy, going tree-ish, as you might say. Most of the trees are just trees, of course; but many are half awake. Some are quite wide awake, and a few are, well, ah, well getting Entish. That is going on all the time. 'When that happens to a tree, you find that some have bad hearts. Nothing to do with their wood: I do not mean that. Why, I knew some good old willows down the Entwash, gone long ago, alas! They were quite hollow, indeed they were falling all to pieces, but as quiet and sweet-spoken as a young leaf. And then there are some trees in the valleys under the mountains, sound as a bell, and bad right through. That sort of thing seems to spread. There used to be some very dangerous parts in this country. There are still some very black patches.' 'Like the Old Forest away to the north, do you mean?' asked Merry. 'Aye, aye, something like, but much worse. I do not doubt there is some shadow of the Great Darkness lying there still away north; and bad memories are handed down... Not everything bad in the world need be controlled by a great evil nor directed towards a single purpose; in this case the trees in the Old Forest are just "bad trees". There are some other interesting references elsewhere in TT: 'We came down over the last ridge into Nan Curunir, after night had fallen,' Merry continued. 'It was then that I first had the feeling that the Forest itself was moving behind us. I thought I was dreaming an entish dream, but Pippin had noticed it too. We were both frightened; but we did not find out more about it until later. 'It was the Huorns, or so the Ents call them in "short language". Treebeard won't say much about them, but I think they are Ents that have become almost like trees, at least to look at. They stand here and there in the wood or under its eaves, silent, watching endlessly over the trees; but deep in the darkest dales there are hundreds and hundreds of them, I believe. 'There is a great power in them, and they seem able to wrap themselves in shadow: it is difficult to see them moving. But they do. They can move very quickly, if they are angry. You stand still looking at the weather, maybe, or listening to the rustling of the wind, and then suddenly you find that you are in the middle of a wood with great groping trees all around you. They still have voices, and can speak with the Ents, that is why they are called Huorns, Treebeard says, but they have become queer and wild. Dangerous. I should be terrified of meeting them, if there were no true Ents about to look after them. (Chapter 9) 'So Saruman would not leave?' he said. 'I did not think he would. His heart is as rotten as a black Huorn's. (Chapter 10) It's quite obvious that these descriptions match nicely with the observed behaviour in the Old Forest, with Old Man Willow being a particularly nasty example (and, of course, with no true Ents around to look after him, he is quite terrifying and dangerous to meet).
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Wealth inequality is escalating at an alarming rate not only within the U.S. but also in countries as diverse as Russia, India and Brazil. According to investment bank Credit Suisse, the fraction of global household wealth held by the richest 1 percent of the world's population increased from 42.5 to 47.2 percent between the financial crisis of 2008 and 2018. To put it another way, as of 2010, 388 individuals possessed as much household wealth as the lower half of the world's population combined—about 3.5 billion people; today Oxfam estimates that number as 26. Statistics from almost all nations that measure wealth in their household surveys indicate that it is becoming increasingly concentrated. Although the origins of inequality are hotly debated, an approach developed by physicists and mathematicians, including my group at Tufts University, suggests they have long been hiding in plain sight—in a well-known quirk of arithmetic. This method uses models of wealth distribution collectively known as agent-based, which begin with an individual transaction between two “agents” or actors, each trying to optimize his or her own financial outcome. In the modern world, nothing could seem more fair or natural than two people deciding to exchange goods, agreeing on a price and shaking hands. Indeed, the seeming stability of an economic system arising from this balance of supply and demand among individual actors is regarded as a pinnacle of Enlightenment thinking—to the extent that many people have come to conflate the free market with the notion of freedom itself. Our deceptively simple mathematical models, which are based on voluntary transactions, suggest, however, that it is time for a serious reexamination of this idea. In particular, the affine wealth model (called thus because of its mathematical properties) can describe wealth distribution among households in diverse developed countries with exquisite precision while revealing a subtle asymmetry that tends to concentrate wealth. We believe that this purely analytical approach, which resembles an x-ray in that it is used not so much to represent the messiness of the real world as to strip it away and reveal the underlying skeleton, provides deep insight into the forces acting to increase poverty and inequality today. Oligarchy In 1986 social scientist John Angle first described the movement and distribution of wealth as arising from pairwise transactions among a collection of “economic agents,” which could be individuals, households, companies, funds or other entities. By the turn of the century physicists Slava Ispolatov, Pavel L. Krapivsky and Sidney Redner, then all working together at Boston University, as well as Adrian Drgulescu, now at Constellation Energy Group, and Victor Yakovenko of the University of Maryland, had demonstrated that these agent-based models could be analyzed with the tools of statistical physics, leading to rapid advances in our understanding of their behavior. As it turns out, many such models find wealth moving inexorably from one agent to another—even if they are based on fair exchanges between equal actors. In 2002 Anirban Chakraborti, then at the Saha Institute of Nuclear Physics in Kolkata, India, introduced what came to be known as the yard sale model, called thus because it has certain features of real one-on-one economic transactions. He also used numerical simulations to demonstrate that it inexorably concentrated wealth, resulting in oligarchy. Credit: Brown Bird Design To understand how this happens, suppose you are in a casino and are invited to play a game. You must place some ante—say, $100—on a table, and a fair coin will be flipped. If the coin comes up heads, the house will pay you 20 percent of what you have on the table, resulting in $120 on the table. If the coin comes up tails, the house will take 17 percent of what you have on the table, resulting in $83 left on the table. You can keep your money on the table for as many flips of the coin as you would like (without ever adding to or subtracting from it). Each time you play, you will win 20 percent of what is on the table if the coin comes up heads, and you will lose 17 percent of it if the coin comes up tails. Should you agree to play this game? You might construct two arguments, both rather persuasive, to help you decide what to do. You may think, “I have a probability of ½ of gaining $20 and a probability of ½ of losing $17. My expected gain is therefore: ½ x ($20) + ½ x (-$17) = $1.50 which is positive. In other words, my odds of winning and losing are even, but my gain if I win will be greater than my loss if I lose.” From this perspective it seems advantageous to play this game. Or, like a chess player, you might think further: “What if I stay for 10 flips of the coin? A likely outcome is that five of them will come up heads and that the other five will come up tails. Each time heads comes up, my ante is multiplied by 1.2. Each time tails comes up, my ante is multiplied by 0.83. After five wins and five losses in any order, the amount of money remaining on the table will be: 1.2 x 1.2 x 1.2 x 1.2 x 1.2 x 0.83 x 0.83 x 0.83 x 0.83 x 0.83 x $100 = $98.02 so I will have lost about $2 of my original $100 ante.” With a bit more work you can confirm that it would take about 93 wins to compensate for 91 losses. From this perspective it seems disadvantageous to play this game. The contradiction between the two arguments presented here may seem surprising at first, but it is well known in probability and finance. Its connection with wealth inequality is less familiar, however. To extend the casino metaphor to the movement of wealth in an (exceedingly simplified) economy, let us imagine a system of 1,000 individuals who engage in pairwise exchanges with one another. Let each begin with some initial wealth, which could be exactly equal. Choose two agents at random and have them transact, then do the same with another two, and so on. In other words, this model assumes sequential transactions between randomly chosen pairs of agents. Our plan is to conduct millions or billions of such transactions in our population of 1,000 and see how the wealth ultimately gets distributed. What should a single transaction between a pair of agents look like? People have a natural aversion to going broke, so we assume that the amount at stake, which we call Δω (Δω is pronounced “delta w”), is a mere fraction of the wealth of the poorer person, Shauna. That way, even if Shauna loses in a transaction with Eric, the richer person, the amount she loses is always less than her own total wealth. This is not an unreasonable assumption and in fact captures a self-imposed limitation that most people instinctively observe in their economic life. To begin with—just because these numbers are familiar to us—let us suppose Δω is 20 percent of Shauna's wealth, ω, if she wins and –17 percent of ω if she loses. (Our actual model assumes that the win and loss percentages are equal, but the general outcome still holds. Moreover, increasing or decreasing Δω will just extend the time scale so that more transactions will be required before we can see the ultimate result, which will remain unaltered.) If our goal is to model a fair and stable market economy, we ought to begin by assuming that nobody has an advantage of any kind, so let us decide the direction in which w is moved by the flip of a fair coin. If the coin comes up heads, Shauna gets 20 percent of her wealth from Eric; if the coin comes up tails, she must give 17 percent of it to Eric. Now randomly choose another pair of agents from the total of 1,000 and do it again. In fact, go ahead and do this a million times or a billion times. What happens? If you simulate this economy, a variant of the yard sale model, you will get a remarkable result: after a large number of transactions, one agent ends up as an “oligarch” holding practically all the wealth of the economy, and the other 999 end up with virtually nothing. It does not matter how much wealth people started with. It does not matter that all the coin flips were absolutely fair. It does not matter that the poorer agent's expected outcome was positive in each transaction, whereas that of the richer agent was negative. Any single agent in this economy could have become the oligarch—in fact, all had equal odds if they began with equal wealth. In that sense, there was equality of opportunity. But only one of them did become the oligarch, and all the others saw their average wealth decrease toward zero as they conducted more and more transactions. To add insult to injury, the lower someone's wealth ranking, the faster the decrease. This outcome is especially surprising because it holds even if all the agents started off with identical wealth and were treated symmetrically. Physicists describe phenomena of this kind as “symmetry breaking” [see The Physics of Inequality below]. The very first coin flip transfers money from one agent to another, setting up an imbalance between the two. And once we have some variance in wealth, however minute, succeeding transactions will systematically move a “trickle” of wealth upward from poorer agents to richer ones, amplifying inequality until the system reaches a state of oligarchy. If the economy is unequal to begin with, the poorest agent's wealth will probably decrease the fastest. Where does it go? It must go to wealthier agents because there are no poorer agents. Things are not much better for the second-poorest agent. In the long run, all participants in this economy except for the very richest one will see their wealth decay exponentially. In separate papers in 2015 my colleagues and I at Tufts University and Christophe Chorro of Université Panthéon-Sorbonne provided mathematical proofs of the outcome that Chakraborti's simulations had uncovered—that the yard sale model moves wealth inexorably from one side to the other. Does this mean that poorer agents never win or that richer agents never lose? Certainly not. Once again, the setup resembles a casino—you win some and you lose some, but the longer you stay in the casino, the more likely you are to lose. The free market is essentially a casino that you can never leave. When the trickle of wealth described earlier, flowing from poor to rich in each transaction, is multiplied by 7.7 billion people in the world conducting countless transactions every year, the trickle becomes a torrent. Inequality inevitably grows more pronounced because of the collective effects of enormous numbers of seemingly innocuous but subtly biased transactions. The Condensation of Wealth You might, of course, wonder how this model, even if mathematically accurate, has anything to do with reality. After all, it describes an entirely unstable economy that inevitably degenerates to complete oligarchy, and there are no complete oligarchies in the world. It is true that, by itself, the yard sale model is unable to explain empirical wealth distributions. To address this deficiency, my group has refined it in three ways to make it more realistic. In 2017 Adrian Devitt-Lee, Merek Johnson, Jie Li, Jeremy Marcq, Hongyan Wang and I, all at Tufts, incorporated the redistribution of wealth. In keeping with the simplicity desirable in applied mathematics models, we did this by having each agent take a step toward the mean wealth in the society after each transaction. The size of the step was some fraction χ (or “chi”) of his or her distance from the mean. This is equivalent to a flat wealth tax for the wealthy (with tax rate χ per unit time) and a complementary subsidy for the poor. In effect, it transfers wealth from those above the mean to those below it. We found that this simple modification stabilized the wealth distribution so that oligarchy no longer resulted. And astonishingly, it enabled our model to match empirical data on U.S. and European wealth distribution between 1989 and 2016 to better than 2 percent. The single parameter χ seems to subsume a host of real-world taxes and subsidies that would be too messy to include separately in a skeletal model such as this one. Credit: Jen Christiansen In addition, it is well documented that the wealthy enjoy systemic economic advantages such as lower interest rates on loans and better financial advice, whereas the poor suffer systemic economic disadvantages such as payday lenders and a lack of time to shop for the best prices. As James Baldwin once observed, “Anyone who has ever struggled with poverty knows how extremely expensive it is to be poor.” Accordingly, in the same paper mentioned above, we factored in what we call wealth-attained advantage. We biased the coin flip in favor of the wealthier individual by an amount proportional to a new parameter, ζ (or “zeta”), times the wealth difference divided by the mean wealth. This rather simple refinement, which serves as a proxy for a multitude of biases favoring the wealthy, improved agreement between the model and the upper tail of actual wealth distributions. The inclusion of wealth-related bias also yields—and gives a precise mathematical definition to—the phenomenon of partial oligarchy. Whenever the influence of wealth-attained advantage exceeds that of redistribution (more precisely, whenever ζ exceeds χ), a vanishingly small fraction of people will possess a finite fraction, 1 − χ/ζ, of societal wealth. The onset of partial oligarchy is in fact a phase transition for another model of economic transactions, as first described in 2000 by physicists Jean-Philippe Bouchaud, now at École Polytechnique, and Marc Mézard of the École Normale Supérieure. In our model, when ζ is less than χ, the system has only one stable state with no oligarchy; when ζ exceeds χ, a new, oligarchical state appears and becomes the stable state [see graphic above]. The two-parameter (χ and ζ) extended yard sale model thus obtained can match empirical data on U.S. and European wealth distribution between 1989 and 2016 to within 1 to 2 percent. Such a phase transition may have played a crucial role in the condensation of wealth following the breakup of the Soviet Union in 1991. The imposition of what was called shock therapy economics on the former states of the U.S.S.R. resulted in a dramatic decrease of wealth redistribution (that is, decreasing χ) by their governments and a concomitant jump in wealth-attained advantage (increasing ζ) from the combined effects of sudden privatization and deregulation. The resulting decrease of the “temperature” χ/ζ threw the countries into a wealth-condensed state, so that formerly communist countries became partial oligarchies almost overnight. To the present day at least 10 of the 15 former Soviet republics can be accurately described as oligarchies. As a third refinement, in 2019 we included negative wealth—one of the more disturbing aspects of modern economies—in our model. In 2016, for example, approximately 10.5 percent of the U.S. population was in net debt because of mortgages, student loans and other factors. So we introduced a third parameter, κ (or “kappa”), which shifts the wealth distribution downward, thereby accounting for negative wealth. We supposed that the least wealth the poorest agent could have at any time was –S, where S equals κ times the mean wealth. Prior to each transaction, we loaned wealth S to both agents so that each had positive wealth. They then transacted according to the extended yard sale model, described earlier, after which they both repaid their debt of S. The three-parameter (χ, ζ, κ) model thus obtained, called the affine wealth model, can match empirical data on U.S. wealth distribution to less than a sixth of a percent over a span of three decades. (In mathematics, the word “affine” describes something that scales multiplicatively and translates additively. In this case, some features of the model, such as the value of Δω, scale multiplicatively with the wealth of the agent, whereas other features, such as the addition or subtraction of S, are additive translations or displacements in “wealth space.”) Agreement with European wealth-distribution data for 2010 is typically better than a third to a half of a percent [see box below]. To obtain these comparisons with actual data, we had to solve the “inverse problem.” That is, given the empirical wealth distribution, we had to find the values of (χ, ζ, κ) at which the results of our model most closely matched it. As just one example, the 2016 U.S. household wealth distribution is best described as having χ = 0.036, ζ = 0.050 and κ = 0.058. The affine wealth model has been applied to empirical data from many countries and epochs. To the best of our knowledge, it describes wealth-distribution data more accurately than any other existing model. Credit: Jen Christiansen; Source: Bruce M. Boghosian; European Central Bank (country data) Trickle Up We find it noteworthy that the best-fitting model for empirical wealth distribution discovered so far is one that would be completely unstable without redistribution rather than one based on a supposed equilibrium of market forces. In fact, these mathematical models demonstrate that far from wealth trickling down to the poor, the natural inclination of wealth is to flow upward, so that the “natural” wealth distribution in a free-market economy is one of complete oligarchy. It is only redistribution that sets limits on inequality. The mathematical models also call attention to the enormous extent to which wealth distribution is caused by symmetry breaking, chance and early advantage (from, for example, inheritance). And the presence of symmetry breaking puts paid to arguments for the justness of wealth inequality that appeal to “voluntariness”—the notion that individuals bear all responsibility for their economic outcomes simply because they enter into transactions voluntarily—or to the idea that wealth accumulation must be the result of cleverness and industriousness. It is true that an individual's location on the wealth spectrum correlates to some extent with such attributes, but the overall shape of that spectrum can be explained to better than 0.33 percent by a statistical model that completely ignores them. Luck plays a much more important role than it is usually accorded, so that the virtue commonly attributed to wealth in modern society—and, likewise, the stigma attributed to poverty—is completely unjustified. Moreover, only a carefully designed mechanism for redistribution can compensate for the natural tendency of wealth to flow from the poor to the rich in a market economy. Redistribution is often confused with taxes, but the two concepts ought to be kept quite separate. Taxes flow from people to their governments to finance those governments' activities. Redistribution, in contrast, may be implemented by governments, but it is best thought of as a flow of wealth from people to people to compensate for the unfairness inherent in market economics. In a flat redistribution scheme, all those possessing wealth below the mean would receive net funds, whereas those above the mean would pay. And precisely because current levels of inequality are so extreme, far more people would receive than would pay. Given how complicated real economies are, we find it gratifying that a simple analytical approach developed by physicists and mathematicians describes the actual wealth distributions of multiple nations with unprecedented precision and accuracy. Also rather curious is that these distributions display subtle but key features of complex physical systems. Most important, however, the fact that a sketch of the free market as simple and plausible as the affine wealth model gives rise to economies that are anything but free and fair should be both a cause for alarm and a call for action.
3.21875
3
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A demographic overview of the ageing of First World populations. The ageing of the UK population, and other similar populations, is now well advanced. The process is probably irreversible and may well be repeated across the globe. It is reasonable to assume that 40-50% of the UK adult population will be over 50 for the foreseeable future, and that the number of people in their 80s and 90s will continue to increase for some decades. Growing awareness of this may well lead to a reinterpretation of the life course with consequent changes in lifestyle and activity. In the past, the main focus of design, both of products and environments, has been the working population. There is clearly an urgent need to direct attention to older sectors of the population, including: fit and active people in retirement; affluent groups in old age; single households; women, who form a majority of the over 50s; and other groups which have been neglected in many work studies.
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The present invention relates generally to systems and methods for controlling an electric motor and, more particularly, to a controller and associated drive assembly for controlling a brushless direct current (BLDC) motor. Electrical machines are used throughout a great number of devices today, and typically consist of motors, which convert electrical energy into mechanical energy, and generators, which convert mechanical energy into electrical energy. Generally, electrical machines fall into one of three categories: polyphase synchronous machines, polyphase asynchronous (i.e., induction) machines and direct current (DC) machines. Typical machines consist of two main portions: a stationary, outside portion called a stator, and a rotating, inner portion called a rotor. The rotor of typical machines is mounted on a stiff rod, or shaft, that is supported in bearings so that the rotor is free to turn within the stator to produce mechanical energy. In one type of synchronous machine, a permanent magnet, brushless direct current (BLDC) machine, the stator is composed of windings that are connected to a controller, and the rotor is composed of two or more permanent magnets of opposed magnetic polarity. The controller includes a driver that generates poly-phase alternating input currents to the stator windings. One conventional driver includes a series of Insulated Gate Bipolar Transistors (IGBT""s) electrically connected to the phase windings of a BLDC motor. For example, for a three-phase BLDC motor, a conventional driver includes six IGBT""s arranged in three half-bridges, where each half-bridge generates a drive for one phase of the motor. As the rotor rotates within the stator, and the magnets of one polarity approach cores of the stator about which the windings are wound, and that conduct the opposed polarity, sensors signal the angular position of the rotor to the controller which, in turn, controls the alternating currents to switch the polarity of the magnetic field produced by windings of the stator. For example, a three-phase BLDC motor can have two, four or more permanent magnets with alternating magnetic polarities mounted on its rotor. The required rotating magnetic field is produced by current through the stator windings. And the three phases of the current are switched in sequence, which is dictated by the angular position of the rotor. In many BLDC motor systems, the speed of the BLDC motor is controlled by the driver pulse modulating, such as pulse width modulating, the input voltage generated by the controller. By pulse-width-modulation (PWM) of the input voltage, the driver and, thus, the controller controls the average input currents to the windings by using xe2x80x9conxe2x80x9d and xe2x80x9coffxe2x80x9d states. During the time the input currents through the windings are increasing, the voltage supply provides constant voltage to the driver at a level at least as high as the motor voltage required for the desired speed of operation. Once the currents have reached the required levels for the desired speed of the motor, the duty cycle is changed to that required to maintain the currents at or near the required level of current. Conventional BLDC motor systems that include a driver comprising a series of IGBT""s are adequate in controlling the speed of BLDC motors at low frequencies. A standard driver including six IGBT""s can drive a three-phase motor (two IGBT""s per phase) with a switching frequency up to approximately 20 kHz if the maximum current is not required for more than a few minutes. In this regard, each IGBT can typically operate with a maximum switching frequency of approximately 20 kHz. Whereas such drivers can control the speed of BLDC motors at low frequencies, such drivers that drive higher power (e.g., greater than one horsepower) and higher voltage (e.g., greater than 200 volts) three-phase motors cannot typically switch at a frequency higher than 20 kHz when the driver comprises IGBT""s. The limit in switching frequency is due to the losses associated with switching the IGBT""s and the average current being switched. What makes the IGBT poor at higher frequencies is that the gate of the transistor is not directly connected to the gate drive circuit (hence insulated gate) and, thus, the electrical charge cannot be quickly removed. The rate at which the electrical charge can be applied or removed fixes the time the IGBT is transitioning between its xe2x80x9coffxe2x80x9d and saturated xe2x80x9conxe2x80x9d states. As the switching frequency increases, the percentage of time that the IGBT is in these transitional regions increases. Also, as current is flowing while the IGBT transitions between states, the power dissipated while the IGBT is in these transitional regions increases. And while other, more advanced products are available that can run at higher frequencies, such products are factors of 50 times more expensive than conventional IGBT""s and are not production items. In light of the foregoing, various embodiments of the present invention provide an improved controller and associated drive assembly for controlling a brushless direct current (BLDC) motor, where the motor includes a predetermined number of phase windings. Various embodiments of the controller and associated drive assembly of the present invention include a plurality of switching elements, such as IGBT""s, arranged such that the power dissipation of a conventional driver is spread among a plurality of drivers. As such, the motor can be driven at a frequency higher than the maximum frequency of any one switching element. Alternatively, the motor can be driven at an operational frequency while operating each switching element at a frequency less than the operational frequency. Thus, the efficiency of the switching elements is increased over conventional drivers. According to one embodiment, a controller for controlling a BLDC motor controller includes a drive assembly, and a processing element. The processing element is in electrical communication with the drive assembly and the BLDC motor, and the processing element is capable of controlling operation of the drive assembly. The drive assembly, on the other hand, is in electrical communication with a power supply and the BLDC motor. As such, the drive assembly is capable of receiving a voltage output of the power supply and is capable of providing a pulse-width-modulated input voltage to the BLDC motor. The drive assembly includes a plurality of half-bridge assemblies that each include two switching elements, such as insulated gate bipolar transistors (IGBT""s), that are each capable of operating at no more than a redetermined frequency. In this regard, at least two half-bridge assemblies are electrically connected to each phase winding of the BLDC motor such that the half-ridge assemblies are capable of providing the pulse-width-modulated input voltage to the respective phase winding of the BLDC motor at a frequency higher than the predetermined frequency. By electrically connecting at least two half-bridge assemblies to each phase winding, the switching elements are each capable of operating at an operating frequency that is less than the predetermined frequency. As such, the half-bridge assemblies that are electrically connected to each phase winding of the BLDC motor are capable of providing the pulse-width-modulated input voltage to the respective phase winding of the BLDC motor at a frequency equal to the product of the number of half-bridge assemblies electrically connected to the respective phase winding and the operating frequency. According to another embodiment, the drive assembly comprises a plurality of drive elements that each include the predefined number of half-bridge assemblies. In this embodiment, each half-bridge assembly of each drive element is electrically connected to a respective phase winding of the BLDC motor. For example, the BLDC motor can include a first, a second and a third phase winding, where the drive assembly comprises a plurality of drive elements that each comprise a first half-bridge assembly, a second half-bridge assembly and a third half-bridge assembly. In this regard, the first half-bridge assemblies can be electrically connected to the first phase winding, the second half-bridge assemblies can be electrically connected to the second phase winding, and the third half-bridge assemblies can be electrically connected to the third phase winding. According to yet another embodiment where the drive assembly comprises a predefined number of drive elements that each comprise a plurality of half-bridge assemblies, each half-bridge assembly of the drive elements is electrically connected to a respective phase winding of the BLDC motor. For example, the BLDC motor can include the first, second and third phase winding. In this regard, the drive assembly can comprise a first, a second and a third drive element that each comprise a plurality of half-bridge assemblies. Thus, the half-bridge assemblies of the first drive element can be electrically connected to the first phase winding, the half-bridge assemblies of the second drive element can be electrically connected to the second phase winding, and the half-bridge assemblies of the third drive element can be electrically connected to the third phase winding.
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Surface plasmon Surface plasmons (SPs) are coherent delocalized electron oscillations that exist at the interface between any two materials where the real part of the dielectric function changes sign across the interface (e.g. a metal-dielectric interface, such as a metal sheet in air). SPs have lower energy than bulk (or volume) plasmons which quantise the longitudinal electron oscillations about positive ion cores within the bulk of an electron gas (or plasma). The charge motion in a surface plasmon always creates electromagnetic fields outside (as well as inside) the metal. The total excitation, including both the charge motion and associated electromagnetic field, is called either a surface plasmon polariton at a planar interface, or a localized surface plasmon for the closed surface of a small particle. The existence of surface plasmons was first predicted in 1957 by Rufus Ritchie. In the following two decades, surface plasmons were extensively studied by many scientists, the foremost of whom were T. Turbadar in the 1950s and 1960s, and Heinz Raether, E. Kretschmann, and A. Otto in the 1960s and 1970s. Information transfer in nanoscale structures, similar to photonics, by means of surface plasmons, is referred to as plasmonics. Surface plasmon polaritons Excitation Surface plasmon polaritons can be excited by electrons or photons. In the case of photons, it cannot be done directly, but requires a prism, or a grating, or a defect on the metal surface. Dispersion relation At low frequency, an SPP approaches a Sommerfeld-Zenneck wave, where the dispersion relation (relation between frequency and wavevector) is the same as in free space. At a higher frequency, the dispersion relation bends over and reaches an asymptotic limit called the "plasma frequency" (see figure at right). For more details see surface plasmon polariton. Propagation length and skin depth As an SPP propagates along the surface, it loses energy to the metal due to absorption. It can also lose energy due to scattering into free-space or into other directions. The electric field falls off evanescently perpendicular to the metal surface. At low frequencies, the SPP penetration depth into the metal is commonly approximated using the skin depth formula. In the dielectric, the field will fall off far more slowly. SPPs are very sensitive to slight perturbations within the skin depth and because of this, SPPs are often used to probe inhomogeneities of a surface. For more details, see surface plasmon polariton. Localized surface plasmons Localize surface plasmons arise in small metallic objects, including nanoparticles. Since the translational invariance of the system is lost, a description in terms of wavevector, as in SPPs, can not be made. Also unlike the continuous dispersion relation in SPPs, electromagnetic modes of the particle are discretized. LSPs can be excited directly through incident waves; efficient coupling to the LSP modes correspond to resonances and can be attributed to absorption and scattering, with increased local-field enhancements. LSP resonances largely depend on the shape of the particle; spherical particles can be studied analytically by Mie theory. Experimental applications The excitation of surface plasmons is frequently used in an experimental technique known as surface plasmon resonance (SPR). In SPR, the maximum excitation of surface plasmons are detected by monitoring the reflected power from a prism coupler as a function of incident angle or wavelength. This technique can be used to observe nanometer changes in thickness, density fluctuations, or molecular absorption. Recent works have also shown that SPR can be used to measure the optical indexes of multi-layered systems, where ellipsometry failed to give a result. Surface plasmon-based circuits have been proposed as a means of overcoming the size limitations of photonic circuits for use in high performance data processing nano devices. The ability to dynamically control the plasmonic properties of materials in these nano-devices is key to their development. A new approach that uses plasmon-plasmon interactions has been demonstrated recently. Here the bulk plasmon resonance is induced or suppressed to manipulate the propagation of light. This approach has been shown to have a high potential for nanoscale light manipulation and the development of a fully CMOS-compatible electro-optical plasmonic modulator, said to be a future key component in chip-scale photonic circuits. Some other surface effects such as surface-enhanced Raman scattering and surface-enhanced fluorescence are induced by surface plasmon of noble metals, therefore sensors based on surface plasmons were developed. In surface second harmonic generation, the second harmonic signal is proportional to the square of the electric field. The electric field is stronger at the interface because of the surface plasmon resulting in a non-linear optical effect. This larger signal is often exploited to produce a stronger second harmonic signal. The wavelength and intensity of the plasmon-related absorption and emission peaks are affected by molecular adsorption that can be used in molecular sensors. For example, a fully operational prototype device detecting casein in milk has been fabricated. The device is based on monitoring changes in plasmon-related absorption of light by a gold layer. See also Biosensor Dual-polarization interferometry Extraordinary optical transmission Free electron model List of plasma (physics) articles Multi-parametric surface plasmon resonance Plasma oscillation Plasmonic lens Spinplasmonics Surface plasmon resonance microscopy Waves in plasmas References Category:Condensed matter physics Category:Plasmonics
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Introduction ============ Red algae (Rhodophyta) form a monophyletic lineage containing \~7,000 described species[@ref1] that exhibit a wide variety of morphological and ultra-structural forms and have complex reproductive strategies. The Cyanidiophytina (e.g., *Galdieria* and *Cyanidioschyzon*) include extremophiles that thrive in volcanic areas surrounding hot springs. In contrast, their mesophilic sisters (Rhodophytina) are globally distributed from freshwater environments to open oceans and deep oceans (\>200 m) to the intertidal zone. Despite a highly reduced core gene inventory that resulted from an ancient phase of genome reduction[@ref2], red algae represent one of the few eukaryotic lineages that have evolved complex multicellularity[@ref3], typified by red seaweeds such as *Porphyra* and *Gracilaria*. Red seaweeds account for \~95% of known red algal taxa and are important sources of agricultural (e.g., *nori*) and industrial products (e.g., agar and carrageenan). Studies of red algal systematics have largely relied on a handful of plastid and nuclear genes[@ref4] ^,^ [@ref5] ^,^ [@ref6] ^,^ [@ref7] ^,^ [@ref8] and focused on a broad diversity of lineages within the Florideophyceae[@ref9] ^,^ [@ref10]. One of the major findings of these analyses is the separation of Cyanidiophytina from the Rhodophytina[@ref4] ^,^ [@ref8]. Whereas Cyanidiophytina contain only two known families (Cyanidiaceae and Galdieraceae), Rhodophytina encompass six classes: Bangiophyceae, Florideophyceae, Compsopogonophyceae, Porphyridiophyceae, Rhodellophyceae, and Stylonematophyceae[@ref4]. Excluding the well-supported monophyly of Bangiophyceae and Florideophyceae (hereafter, collectively referred to as red seaweeds), relationships among the remaining classes remain controversial[@ref4] ^,^ [@ref5] ^,^ [@ref6] ^,^ [@ref7] ^,^ [@ref8]. In this study, we applied phylogenomics to a rich genomic dataset to erect a robust red algal tree of life. The dataset encompassed 298 orthologous nuclear-encoded genes from all major red algal lineages. In contrast to previous phylogenies built using smaller datasets[@ref4] ^,^ [@ref5] ^,^ [@ref6] ^,^ [@ref7] ^,^ [@ref8], our results support a fundamental, ancient split between red seaweeds and non-seaweed lineages among mesophiles. We discuss the implication of this new perspective on red algal phylogeny to understanding the evolution of multicellularity in red algae, and demonstrate the utility of this phylogenetic framework to infer the evolution of the mevalonate (MVA) pathway of isoprenoid biosynthesis in Rhodophyta. Methods ======= **Construction of single-copy orthologous gene alignments** We created a local database that includes protein sequences (translated from EST or predicted from genome sequences) from 15 red algal taxa[@ref2] ^,^ [@ref11] ^,^ [@ref12] ^,^ [@ref13] ^,^ [@ref14] ^,^ [@ref15] ^,^ [@ref16] ([Fig. 1A](#figure1){ref-type="fig"}) and 3 green algae[@ref17] ^,^ [@ref18] ^,^ [@ref19] ([Table 1](#table1){ref-type="table"}, Appendix 1). This database, after removing short sequences with length \<100 amino acids, was used in a self-query using BLASTp (*e*-value cutoff = 1e-5). The BLASTp search output was used as input for OrthoMCL[@ref20] with parameters (evalueExponentCutoff = -10, percentMatchCutoff = 40, inflation = 1.5) to construct orthologous gene families. Among these families, we searched for single-copy orthologous genes with one gene copy per species (allowing missing data in up to three red algae and in no more than one green alga). For each orthologous gene family, the corresponding sequences were retrieved and aligned using MUSCLE (version 3.8.31) under the default settings[@ref21]. The alignments were then trimmed using TrimAl (version 1.4)[@ref22] in automated mode (-automated) and then 'polished' with T-COFFEE (version 9.03)[@ref23] to removed poorly aligned residues (conservation score ≤ 5) among the aligned blocks. A total of 298 single-gene alignments (length \>150 amino acids and with ≥15 sequences) were retained for downstream analysis. **Construction of the multi-protein phylogeny** The 298 single-copy gene alignments were concatenated into a super-protein alignment. A phylogenetic tree was inferred using Phylobayes (version 3.3)[@ref24] under the CAT model[@ref25]. This is a mixture model that takes into consideration site-specific evolutionary properties (such as rate and profile) within the alignment[@ref25]. The CAT model generally fits data significantly better than one-matrix models such as LG and WAG. We set up two chains that ran in parallel and assessed convergence periodically using 'bpcomp' and 'tracecomp' functions. Convergence assessments were done based on sampled trees (taking one from every 10 trees) following burnin equal to 20% of the entire length of the chain. The two chains were stopped when they converged to an acceptable level that allows good qualitative measurement of the posterior consensus. According to the user instructions (www.phylobayes.org/), an acceptable run corresponds to a maximum discrepancy across all bipartitions (maxdiff \<0.3) when monitored with the 'bpcomp' function, and statistical discrepancies \<0.3 and effective sizes \>50 for all parameters when monitored with the 'tracecomp' function. **Construction of coalescence model-based species trees** We built a coalescence model-based red algal phylogeny with 100 replicates following Seo\'s method[@ref26]. For each replicate, we randomly sampled 298 genes with replacement. For each sampled alignment, a pseudo-alignment was generated by random sampling of amino acid site from the original alignment with replacement. Only one green algal sequence (as outgroup) was retained with the priority given to *Chlamydomonas reinhardtii*, *Chlorella variabilis*, and *Micromonas*RCC299 in order. A ML tree was built for each pseudo-alignment using IQtree (version 0.9.6)[@ref27] under the best-fit amino acid evolutionary model selected on the fly (-m TEST). The resulting 298 ML trees, rooted with outgroup sequences, were then used for maximum pseudo-likelihood tree construction using MP-EST (version 1.4) under the default settings[@ref28]. This procedure was repeated 100 times and the resulting 100 maximum pseudo-likelihood trees were summarized under majority rule using the 'consense' function in Phylip (http://evolution.genetics.washington.edu/phylip.html). **Phylogenetic analyses of mevalonate pathway genes** *Galdieria sulphuraria* proteins in the MVA pathway (module identifier: M00095) and the methylerythritol phosphate (MEP) pathway (module identifier: M00096) were retrieved from the KEGG database[@ref29] and used as queries against NCBI (nr) using BLASTp (*e*-value cutoff = 1e-5) (http://blast.ncbi.nlm.nih.gov/Blast.cgi). The representative sequences (e.g., from Metazoa and land plants) were retrieved from Genbank. Local BLASTp searches (*e*-value cutoff = 1e-5) were done against our red algal database aforementioned followed by retrieval of the significant hits. *Galdieria phlegrea* sequences were retrieved from the previous study[@ref30]. Each *G. sulphuraria* query, together with the homologs (from Genbank and our local database), were aligned using MUSCLE (version 3.8.31)[@ref21] under the default settings. The alignment was trimmed using trimAl (version 1.4)[@ref22] in the automated mode (-automated). ML trees were built using IQtree (version 0.9.6)[@ref27] under the best amino acid evolutionary model selected using (-m TEST) with branch support values estimated using 1,500 ultrafast bootstrap replicates (-bb 1500). The resulting trees were manually inspected. Distantly related paralogs (if any) were removed manually and the trees were rebuilt following the procedure described above. **Validation of gene losses in red algae** We searched for the *G. sulphuraria* MVA and MEP proteins in a red algal nucleotide database (genome and transcriptome) using tBLASTn (*e*-value cutoff = 1e-5). The homologous protein sequences translated from the hit nucleotide sequences were collected using an in-house script. For each query sequence, the translated proteins corresponding to the three top bit-score hits and the three top-identity (query-hit identity) hits were incorporated into the single-gene ML tree building procedure described above. Distantly related homologs were manually identified and removed. Red algal sequences that were monophyletic with *G. sulphuraria* were considered to be orthologs. Results and Discussion ====================== **Red algal tree of life** We constructed single-gene alignments for a total of 298 one-to-one orthologous genes (98,494 amino acid positions in total) that are conserved in 15 red algal and 3 green algal taxa (see Methods). Analysis of the concatenated super-protein alignment under the CAT model led to a highly supported phylogenetic tree that received 1.00 posterior probability for all interior nodes ([Fig. 1A](#figure1){ref-type="fig"}). This tree confirmed the early split between Cyanidiophytina and Rhodophytina[@ref4] ^,^ [@ref8] and monophyletic relationship between Bangiophyceae and Florideophyceae[@ref4] ^,^ [@ref8]. The relationships within Florideophyceae are consistent with previous analyses[@ref10] ^,^ [@ref31] with Hildenbrandiophycidae (*Hildenbrandia*) in the basal position. Nemaliophycidae (*Palmaria*) is sister to the monophyletic group containing Corallinophycidae (*Calliarthron*) and Rhodymeniophycidae (*Chondrus*)[@ref10] ^,^ [@ref31]. The remaining non-seaweed mesophilic lineages formed a robust monophyletic group, with Stylonematophyceae in the basal position. Compsopogonophyceae formed a sister group to the monophyletic Porphyridiophyceae and Rhodellophyceae. Concatenation-based analysis has previously been shown in some instances to result in inflated statistical support for incorrect topologies[@ref32] due to heterogeneity across genes and gene-specific evolution, such as gene duplication[@ref33]. To minimize this problem, we used a tree summarization approach that does not rely on the concatenation of multiple single-gene alignments. This method takes a population of single-gene trees as input and estimates the species tree using a coalescence model[@ref28]. This analysis led to the same tree topology ([Fig. 1A](#figure1){ref-type="fig"}) to the concatenation-based analysis with high bootstrap support for the monophyletic group comprising red seaweeds (bootstrap support = 100%) and non-seaweed mesophilic red algae (bootstrap support = 90%). The relationships among non-seaweed red algal lineages are however weakly supported (bootstrap support = 49-51%). Taken together, our phylogenomic analyses strongly support a separation between seaweeds and non-seaweed lineages at the base of mesophilic red algae ([Fig. 1A](#figure1){ref-type="fig"}). Red algal phylogenomics(A) A phylogenetic tree inferred from a concatenated 298-protein alignment. The outgroup species are not shown. Statistical supports (separated by a back slash) for each branch are derived from the super-protein analysis (posterior probability) and from the coalescence model-based analysis (bootstrap support). (B) Schematic representation of the positions of red seaweeds and land plants (thick branches) in red algae and Viridiplantae, respectively. The phylogenies are derived from this study (panel I), Scott et al (Ref. 6, panel II) and Leliaert et al. (Ref. 35, panel III). The arrows indicate genome reduction (GR). Bangiophyceae (Bangio.), Compsopogonophyceae (Compsopogo.), Cyanidiophyceae (Cyanidio.), Florideophyceae (Florideo.), Porphyridiophyceae (Porphyridio.), Stylonematophyceae (Stylonemato.), Coleochaetophyceae (Coleochaeto.), Chlorokybophyceae (Chlorokybo.), Klebsormidiophyceae (Klebsormidio.), Mesostigmatophyceae (Mesostigmato.), Zygnematophyceae (Zygnemato.).(A) A phylogenetic tree inferred from a concatenated alignment of 298-proteins. The outgroup species are not shown. Statistical supports (separated by a back slash) for each branch are derived from the super-protein analysis (posterior probability) and from the coalescence model-based analysis (bootstrap support). (B) Schematic representation of the positions of red seaweeds and land plants (thick branches) in red algae and Viridiplantae, respectively. The phylogenies are derived from this study (panel I), Scott et al (Ref. 6, panel II) and Leliaert et al. (Ref. 35, panel III). The arrows indicate genome reduction (GR). Bangiophyceae (Bangio.), Compsopogonophyceae (Compsopogo.), Cyanidiophyceae (Cyanidio.), Florideophyceae (Florideo.), Porphyridiophyceae (Porphyridio.), Stylonematophyceae (Stylonemato.), Coleochaetophyceae (Coleochaeto.), Chlorokybophyceae (Chlorokybo.), Klebsormidiophyceae (Klebsormidio.), Mesostigmatophyceae (Mesostigmato.), Zygnematophyceae (Zygnemato.).(A) A phylogenetic tree inferred from a concatenated alignment of 298-proteins. The outgroup species are not shown. Statistical supports (separated by a back slash) for each branch are derived from the super-protein analysis (posterior probability) and from the coalescence model-based analysis (bootstrap support). (B) Schematic representation of the positions of red seaweeds and land plants (thick branches) in red algae and Viridiplantae, respectively. The phylogenies are derived from this study (panel I), Scott et al (Ref. 6, panel II) and Leliaert et al. (Ref. 35, panel III). The arrows indicate genome reduction (GR). Bangiophyceae (Bangio.), Compsopogonophyceae (Compsopogo.), Cyanidiophyceae (Cyanidio.), Florideophyceae (Florideo.), Porphyridiophyceae (Porphyridio.), Stylonematophyceae (Stylonemato.), Coleochaetophyceae (Coleochaeto.), Chlorokybophyceae (Chlorokybo.), Klebsormidiophyceae (Klebsormidio.), Mesostigmatophyceae (Mesostigmato.), Zygnematophyceae (Zygnemato.). **Parallel losses of MVA pathway** To demonstrate the usefulness of this novel perspective on red algal phylogeny, we used the reference tree to elucidate the evolution of the isopentenyl pyrophosphate (IPP) biosynthetic pathway. IPP is the building block of isoprenoids that comprises a large diversity of lipids found in all three domains of life. In photosynthetic eukaryotes, two independent pathways exist to produce IPP, the cytosolic and peroxisome localized MVA pathway and the plastid MEP pathway[@ref38]. Whereas the MEP pathway is conserved across many species, the MVA pathway has been lost in green algae (Chlorophyta)[@ref38] and in some red algal lineages such as *C.* *merolae* [@ref16] and *P. purpureum* [@ref12]. Our analysis of red algal sequence data (see Methods) showed that the MEP pathway is present in all examined lineages. The minor gene losses that were found are most likely to be explained by missing data commonly associated with transcriptome datasets ([Fig. 3](#figure3){ref-type="fig"}, Appendix 2). In contrast, the MVA pathway is largely absent (3rd to 6th enzymes in the pathway, [Fig. 2A](#figure2){ref-type="fig"}) in most red algal lineages except the Stylonematophyceae (*Rhodosorus marinus* and *Purpureofilum apyrenoidigerum*) and *G. sulphuraria*. Presence of the MVA pathway in *G. sulphuraria* [@ref39] and *Cyanidium caldarium* [@ref40] is supported with genetic and biochemical evidence[@ref39] ^,^ [@ref40]. This result suggests that loss of MVA pathway is more widespread than previously thought. The red algal origin of the MVA genes in Stylonematophyceae is supported with phylogenetic data (see Methods). For example, in the phylogeny of HMG-CoA reductase (HMGR, [Fig. 2B](#figure2){ref-type="fig"}), *R. marinus* and *P. apyrenoidigerum* form a monophyletic group with and *Galdieria* species, whereas no other red algae were present in this clade. A similar pattern is found for other MVA pathway genes that were lost in most red algal species ([Fig. 4](#figure4){ref-type="fig"}, Appendix 3). MVA pathway in red algae(A) The distribution of MVA pathway genes across red algal species. Black and open circles denote the presence and absence of the genes, respectively. For each gene, the gray boxes indicate gene presence for the corresponding classes. Arrows indicate genome reduction. Red vertical bars indicate gene losses. ACAT (acetyl-CoA acetyltransferase), HMGS (hydroxymethylglutaryl-CoA synthase), HMGR (3-hydroxy-3-methylglutaryl-CoA reductase), MVK (mevalonate kinase), PMK (phosphomevalonate kinase), MVD (mevalonate decarboxylase), IDI (isopentenyl-diphosphate delta-isomerase). (B) A ML tree of HMGR. The taxa in red color: red algae, green: Viridiplantae, orange: chromalveolates, brown: Opisthokonta.Figure2 Absence of the MVA pathway in all five sampled red seaweeds suggests it was most likely lost in their common ancestor. BLASTp searches (*e*-value cutoff = 10) against nucleotide databases (expressed sequence tag and transcriptome shotgun assembly) in NCBI did not return any significant hits to MVA pathway genes from Bangiophyceae and Florideophyceae. In addition, their losses in *C. merolae*, *P. purpureum*, and *C. crispus*that have both transcriptome and genome data available are well supported. Given the red algal phylogeny ([Fig. 1A](#figure1){ref-type="fig"}), these losses were unambiguously resulted from three parallel events ([Fig. 2A](#figure2){ref-type="fig"}). Under this scenario, the MVA pathway survived the ancient phases of genome reduction (arrows, [Fig. 2A](#figure2){ref-type="fig"}) and underwent gene loss more recently after the split of the seaweed and non-seaweed lineages. MVA pathway loss in *C. merolae*likely resulted from an additional phase of genome reduction specific to this lineage[@ref30] ([Fig. 2A](#figure2){ref-type="fig"}). The selective forces that led to the retention or loss of the MVA pathway across the mesophilic red algal lineages are presently unknown. Nonetheless, MVA pathway loss suggests that IPP biosynthesis is dependent on the plastid MEP pathway and requires transporters for the export of IPP from the plastid to the cytosol[@ref38]. The MVA pathway was also lost in Chlorophyta (including most unicellular green algae)[@ref38] and *G. sulphuraria*is physiologically distinct from mesophilic species. For this reason, the discovery of possible MVA pathway-containing and -absent lineages among mesophilic red algae provides an algal model for studying the evolution of isoprenoid biosynthesis and intracellular trafficking among compartments. Conclusion ========== Our phylogenomic analyses resulted in a well-supported red algal phylogeny that provides new insights into the evolution of red seaweeds. Our results will allow more accurate reconstruction of evolutionary events (e.g., gene family evolution[@ref2] and molecular calibration[@ref10]) and provide a framework to map the distribution of red algal functions and traits. Further efforts are needed to substantiate the relationships among non-seaweed mesophilic red algae with high quality genome data from these taxa[@ref41]. Data Availability ================= The multi-protein alignment is available for download (ID: 20087) from TreeBASE (https://treebase.org). Competing Interests =================== The authors have declared that no competing interests exist. Corresponding Author ==================== Huan Qiu, Department of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, NJ 08901, USA. E-mail: huan.qiu.bio\@gmail.com Appendix 1 ========== Table 1Algal genome and transcriptome data used for the phylogenomic analysisClassificationSpeciesSourceData typeMMETSP IDSeaweedHildenbrandia rubraRef. 2Transcriptome-SeaweedPalmaria palmataRef. 2Transcriptome-SeaweedCalliarthron tuberculosumRef. 14Partial genome-SeaweedChondrus crispusRef. 13Whole genome-SeaweedPorphyra umbilicalisRef. 14Transcriptome-MesophilesPurpureofilum apyrenoidigerumRef. 2Transcriptome-MesophilesRhodochaete pulchellaRef. 2Transcriptome-MesophilesRhodosorus marinusRef. 11TranscriptomeMMETSP0315MesophilesRhodella maculataRef. 11TranscriptomeMMETSP0167MesophilesCompsopogon coeruleusRef. 11TranscriptomeMMETSP0312MesophilesErythrolobus australicusRef. 11TranscriptomeMMETSP1353MesophilesTimspurckia oligopyrenoidesRef. 11TranscriptomeMMETSP1172MesophilesPorphyridium purpureumRef. 12Transcriptome-ExtremophilesGaldieria sulphurariaRef. 15Transcriptome-ExtremophilesCyanidioschyzon merolaeRef. 16Whole genome-Green algaeChlorella variabilisRef. 17Whole genome-Green algaeChlamydomonas reinhardtiiRef. 18Whole genome-Green algaeMicromonas pusillaRef. 19Whole genome- Appendix 2 ========== Distribution of the MEP pathway across red algal lineagesBlack and open circles denote the presence and absence of the genes, respectively. For each gene, the gray boxes indicate the gene presence for the corresponding classes. DXS (1-deoxy-d-xylulose 5-phosphate synthase), DXR (1-deoxy-d-xylulose 5-phosphate reductoisomerase), MCT (2-C-methyl-d-erythritol 4-phosphate cytidylyltransferase), CMK (C-methyl-d-erythritol kinase), MDS (2-C-methyl-d-erythritol 2,4-cyclodiphosphate synthase), HDS (4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase), HDR (4-hydroxy-3-methylbut-2-en-1-yl diphosphate reductase), IDI (isopentenyl-diphosphate isomerase).FigureS2 Appendix 3 ========== ML trees for six MVA pathway genesThe taxa in red color: red algae, green: Viridiplantae, orange: chromalveolates, brown: Opisthokonta.The taxa in red color: red algae, green: Viridiplantae, orange: chromalveolates, brown: Opisthokonta. The authors would like to thank the editor and reviewer for their valuable comments and suggestions to improve the manuscript.
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Ethical dilemmas of a driverless world University of Auckland's Alex Sims looks at why we can't apply a universal code of ethics to driverless cars Results from a huge online game designed to show whether people across the globe think the same about decisions a driverless car should take in the face of an unavoidable accident has been published in Nature, the leading international science journal. The game, Moral Machine Experiment, has echoes of the “trolley problem” which was once just a thought experiment in ethics. The problem goes like this: You see a runaway trolley (in New Zealand we would describe it as a train carriage), moving towards five people lying on train tracks. Next to you is a lever that controls a switch. If you pull the lever the trolley will be diverted onto another set of tracks, saving the five people. But there is one person lying on the other set of tracks and pulling the lever will kill that person. Which one is ethically correct? Autonomous cars raise the stakes. If a crash is inevitable, for example, an autonomous car's brakes fail, and the car has to choose between running over and killing three elderly people or swerving into a brick wall and killing the car’s occupants, what should the car do? The authors state, quite rightly, that we as a society cannot leave the ethical principles to either engineers or ethicists. We need rules. It would be unconscionable for people to drive cars that were programmed to ensure the occupant’s safety was put ahead of everyone else. For example, a car cannot be programmed to run three people over to avoid the car’s sole occupant crashing into a parked car. The Moral Machine Experiment, by MIT (Massachusetts Institute of Technology), collected nearly 40 million decisions from respondents in 233 countries. The project’s scope was ambitious as it sought to explore whether a universal machine ethics was possible. While the authors acknowledged the limitations of the study, for example, significantly more men responded to the survey than women, nonetheless the number of respondents and their spread across the world made a welcome change from experiments carried out on college students in the United States. The game presented different scenarios which focused on nine factors: sparing humans (versus pets), staying on course (versus swerving), sparing passengers (versus pedestrians), sparing more lives (versus fewer lives), sparing men (versus women), sparing the young (versus the elderly), sparing pedestrians who cross legally (versus jaywalking), sparing the fit (versus the less fit), and sparing those with higher social status (versus lower social status). Four levels of analysis were used. First, what is the relative importance of the nine factors, when data are aggregated worldwide? Second, does the intensity of each preference depend on respondents’ individual characteristics? Third, can clusters of countries with homogeneous moral preferences be identified? And fourth, do cultural and economic variations between countries predict variations in their moral preferences? While there were differences between countries, the research found three strong preferences: saving human lives over the lives of animals; sparing more lives, and sparing young lives. Respondents from individualistic cultures had a stronger preference for sparing the greatest number of people. Those from collectivistic cultures showed a weaker preference for saving younger people, which is not surprising given the respect they show to older members of their society. The study found that countries could be grouped into three clusters in terms of moral preferences. The first cluster was Western, in addition to New Zealand it included North America, with a number of European countries as well as sub-clusters containing Scandinavian countries and Commonwealth countries. The second was Eastern, including Japan, China, and Taiwan as well as Islamic countries such as Indonesia, Pakistan and Saudi Arabia. The third was Southern, which was the Latin American countries as well as France and those that had a French influence. There were differences between the clusters which make for fascinating reading. Respondents from countries with a strong rule of law were more likely to spare more characters, to favour humans over non-humans and less likely to favour higher-status over lower status people. Also, respondents from countries with a higher socio-economic inequality (measured by the Gini-coefficient) were more likely to spare higher-status people over lower status people. Thus the danger is that in the latter countries autonomous cars would protect their wealthy owners at the expense of others. Respondents from individualistic cultures had a stronger preference for sparing the greatest number of people. Those from collectivistic cultures showed a weaker preference for saving younger people, which is not surprising given the respect they show to older members of their society. Curiously while the authors were seeking to see if a universal machine ethics was possible, and they found there were common preferences, they do not argue for a universal machine ethic, rather that each country will set their own ethics. Moreover, the authors note that ethical preferences should not necessarily dictate the ethical policy adopted, albeit the people’s willingness to buy autonomous vehicles and tolerate their use will depend on the palatability of the rules adopted. To be sure, the authors are being pragmatic because attempting to impose a universal machine ethics would be difficult, but decisions are going to need to be made, such as whether the lives of a few should be sacrificed to save many. It should not be left open to individual car companies, as has been proposed in the ethical rules proposed in 2017 by the German Ethics Commission on Automated and Connected Driving that simply says that “General programming to reduce the number of personal injuries may be justifiable”. However, on an equally pragmatic note: what happens when you drive a car from one country to another country with different rules? The car would be required to update its operating system to adjust to the new country’s rules, which would not necessarily always go smoothly. And what of the law? Ethical rules are interesting as there is often a large difference between ethical and legal rules. Breaking a legal rule can result in many sanctions, for example, being fined and imprisoned and even not being able to travel to certain countries as well as difficulty finding employment and obtaining insurance. Ethical breaches do not incur the same sanctions. While some legal rules are ethically based – such as do not steal – others are not. For example, legally as an employer you are entitled to pay your employees the minimum wage when you know they are going without food so that their children eat, even though ethically you should pay them more as you are making extremely large profits. Thus when the “ethical” rules are determined, these rules must be enshrined in law. While the ethical issues are problematic it must be borne in mind that currently over one million people die each year as a result of car crashes and tens of millions are injured. Autonomous cars will greatly diminish the number of fatalities and injuries, which can only be a good thing. Also, we must remember that new technology is always viewed with suspicion. In the United Kingdom, the first cars were limited to a speed of four miles per hour on public highways and two miles an hour in cities, towns and villages. A person was required to walk in front of the car carrying a red flag to warn riders and drivers of horses about the oncoming vehicle. Newsroom is powered by the generosity of readers like you, who support our mission to produce fearless, independent and provocative journalism. Comments Newsroom does not allow comments directly on this website. We invite all readers who wish to discuss a story or leave a comment to visit us on Twitter or Facebook. We also welcome your news tips and feedback via email: contact@newsroom.co.nz. Thank you.
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Scaling pattern of occupancy In spatial ecology and macroecology, scaling pattern of occupancy (SPO), also known as the area-of-occupancy (AOO) is the way in which species distribution changes across spatial scales. In physical geography and image analysis, it is similar to the modifiable areal unit problem. Simon A. Levin (1992) states that the problem of relating phenomena across scales is the central problem in biology and in all of science. Understanding the SPO is thus one central theme in ecology. Pattern description This pattern is often plotted as log-transformed grain (cell size) versus log-transformed occupancy. Kunin (1998) presented a log-log linear SPO and suggested a fractal nature for species distributions. It has since been shown to follow a logistic shape, reflecting a percolation process. Furthermore, the SPO is closely related to the intraspecific occupancy-abundance relationship. For instance, if individuals are randomly distributed in space, the number of individuals in an α-size cell follows a Poisson distribution, with the occupancy being Pα = 1 − exp(−μα), where μ is the density. Clearly, Pα in this Poisson model for randomly distributed individuals is also the SPO. Other probability distributions, such as the negative binomial distribution, can also be applied for describing the SPO and the occupancy-abundance relationship for non-randomly distributed individuals. Other occupancy-abundance models that can be used to describe the SPO includes Nachman's exponential model, Hanski and Gyllenberg's metapopulation model, He and Gaston's improved negative binomial model by applying Taylor's power law between the mean and variance of species distribution, and Hui and McGeoch's droopy-tail percolation model. One important application of the SPO in ecology is to estimate species abundance based on presence-absence data, or occupancy alone. This is appealing because obtaining presence-absence data is often cost-efficient. Using a dipswitch test consisting of 5 subtests and 15 criteria, Hui et al. confirmed that using the SPO is a robust and reliable for assemblage-scale regional abundance estimation. The other application of SPOs includes trends identification in populations, which is extremely valuable for biodiversity conservation. Explanation Models providing explanations to the observed scaling pattern of occupancy include the fractal model, the cross-scale model and the Bayesian estimation model. The fractal model can be configured by dividing the landscape into quadrats of different sizes, or bisecting into grids with special width-to-length ratio (2:1), and yields the following SPO: where D is the box-counting fractal dimension. If during each step a quadrat is divided into q sub-quadrats, we will find a constant portion (f) of sub-quadrats is also presence in the fractal model, i.e. D = 2(1 + log ƒ/log q). Since this assumption that f is scale independent is not always the case in nature, a more general form of ƒ can be assumed, ƒ = q−λ (λ is a constant), which yields the cross-scale model: The Bayesian estimation model follows a different way of thinking. Instead of providing the best-fit model as above, the occupancy at different scales can be estimated by Bayesian rule based on not only the occupancy but also the spatial autocorrelation at one specific scale. For the Bayesian estimation model, Hui et al. provide the following formula to describe the SPO and join-count statistics of spatial autocorrelation: where Ω = p(a)0 − q(a)0/+p(a)+ and  = p(a)0(1 − p(a)+2(2q(a)+/+ − 3) + p(a)+(q(a)+/+2 − 3)). p(a)+ is occupancy; q(a)+/+ is the conditional probability that a randomly chosen adjacent quadrat of an occupied quadrat is also occupied. The conditional probability q(a)0/+ = 1 − q(a)+/+ is the absence probability in a quadrate adjacent to an occupied one; a and 4a are the grains. The R-code of the Bayesian estimation model has been provided elsewhere . The key point of the Bayesian estimation model is that the scaling pattern of species distribution, measured by occupancy and spatial pattern, can be extrapolated across scales. Later on, Hui provides the Bayesian estimation model for continuously changing scales: where b, c, and h are constants. This SPO becomes the Poisson model when b = c = 1. In the same paper, the scaling pattern of join-count spatial autocorrelation and multi-species association (or co-occurrence) were also provided by the Bayesian model, suggesting that "the Bayesian model can grasp the statistical essence of species scaling patterns." Implications for biological conservation The probability of species extinction and ecosystem collapse increases rapidly as range size declines. In risk assessment protocols such as the IUCN Red List of Species or the IUCN Red List of Ecosystems, area of occupancy (AOO) is used as a standardized, complementary and widely applicable measure of risk spreading against spatially explicit threats. References Category:Conservation biology Category:Population ecology Category:Environmental statistics
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The struggle to remind the world of what happened in Nanjing in 1937. From photographer Amanda Mustard. Photographer Amanda Mustard followed a long chain of contacts and helpers to arrive at her project on the survivors of the Nanjing Massacre. It started with her high school history teacher, who led her to read The Rape of Nanking by the late Iris Chang, whose mother would later help Mustard break down barriers and locate a handful of the last survivors of one of the most brutal chapters of World War II. This Friday marks the 76th anniversary of the day Japan captured the then-capital of China and put its people to the sword. Some 300,000 people in the city died—most of them during the first six weeks of the occupation—according to Chinese estimates. There were international as well as Chinese witnesses to the unhinged grotesquerie of rape, lawlessness and murder, but to this day, Japan refuses to formally apologize. This intransigence has become a constant rallying cry for Chinese nationalists and an ongoing point of friction between two wary powers. A crime on the scale of Nanjing is, at root, a constellation of individual tragedies. Which is why Mustard’s project, shot during the 75th anniversary last year, has such appeal. By the time Mustard flew from Cairo to Nanjing for this this work, only 200 survivors were still alive. It falls to them to keep the memory real, but in their old age, many face other challenges. They have been lauded as ‘war heroes’ by the Chinese government, which is keen to use them as reminders of Japan’s perfidy. But then there are stories like that of Cheng Yun, who is photographed below. His service as a Chinese solider in occupied Nanjing is celebrated at memorial events, but he has also been denied military pension benefits because he had been deemed anti-Communist earlier in life. At 93, he now survives by recycling bottles in a Nanjing slum, and is provided daily meals and care by his nephew. And so his story, like China’s, is still evolving, reminders not just of a terrible past, but also of a contemporary China that still struggles to provide dignity and freedom to all its people. The survivors of Nanjing have suffered too much to deserve anything less. Only three of the Chinese military troops who survived the Japanese occupation of Nanjing are still alive. Li Gaoshan is one of them. Cheng Yun’s ID shows that he graduated from Whampao Military Academy. But due to his anti-Communist past, Cheng, 92, is now classified as a farmer and not a soldier, so that he receives no pension. In December 1937, Japanese forces first entered the city at Zhongshan Gate, the strongest point of defense in the old city walls of Nanjing. Cao Zhikun barely escaped death with his family during Japanese occupation, and struggled for decades with both physical and mental scars. Approximately 15,100 Chinese civilians and soliders were buried under a section of Xiuqui Park. People’s Liberation Army and Navy troops stand with civilians at Nanjing’s Memorial Hall to commemorate the 75th anniversary of the Nanjing Massacre. Survivor Cao Zhikun holds a portrait of his family taken two weeks before the massacre began. Citizens cross the Yangtze River via ferry from the Zhongshan Wharf. An estimated 150,000 bodies were dumped in this stretch of river and embankment during the massacre. The images of hundreds of survivors are illuminated at the Memorial Hall in Nanjing. As of 2012, less than 200 survivors remained. Cheng Yun, a soldier who lived through the Japanese occupation, stands outside his home in Nanjing. A rabbit in a Nanjing slum that was, before the Japanese invasion, a wealthy district. Survivor Li Jun, his family, and 600 others took refuge in the yard of John Rabe, a German executive for Siemens and Nazi party member, who established the International Safety Zone in Nanjing, saving the lives of over 250,000 Chinese.
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Q: What is the usage of super keyword here? I have a piece of code def data data_type == 'option' ? options[super.to_i] : super end I cannot figure out from where the super keyword is getting the value. A: Here super keyword calls the same data method of its parent class if data_type == 'option' is false. Check this link for a detailed explanation. Super keyword in Ruby Update: The above code can be re-written as if data_type == 'option' options[super.to_i]#options is probably a hash/array here. else super end When we call super it returns a value after executing it's parent class's data method, lets assume it returned "5", we're converting that to an integer and getting data out of options array. i.e., options[5]. In the else block we're simply returning the the value parent's data method got us.
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FREE eBook: Stargazing: Getting Started Crowded Clusters Host Planets The discovery of two mini-Neptunes around Sun-like stars in a distinctly un-Sun-like environment reveals that small planets can live in more crowded neighborhoods than we thought. An artist's rendition of a mini-Neptune in a cluster packed with bright, young stars. Michael Bachofner Most stars form in clusters. Those stars, and the planets they host, grow up surrounded by tens or even thousands of stellar siblings born from the same gas cloud. In the jostling for space, it’s a wonder any planets survive. The question is, how dense is too dense? Answering that question has been difficult: until now, astronomers had detected only four planets inside clusters, compared to more than 850 planets found orbiting isolated stars in the galactic field. But Soren Meibom (Harvard-Smithsonian Center for Astrophysics) and a team of astronomers recently reported in Nature two mini-Neptunes inside a dense cluster, showing that even stars in the densest clusters can form planets. The two planets, Kepler 66-b and Kepler 67-b, are slightly smaller than Neptune, each almost three times as wide as Earth. They closely circle Sun-like stars, whipping around every 17.8 and 15.2 days, respectively. But their environment is anything but Sun-like. They live in NGC 6811, a billion-year-old open cluster that was once jam-packed with more than 6,000 stars. The Sun also grew up in an open cluster. But the Sun’s birthplace was 100 times less dense than NGC 6811, and the surrounding stars went their separate ways over the course of several million years, maybe even before the stars and planets had finished forming. NGC 6811, on the other hand, survived to the present-day, even though it lost some members to gravitational interactions or supernova explosions. In the jam-packed environs of an open cluster, countless dangers await a forming planet. A gravitational bump from a passing star could disrupt the protoplanetary disk or nearby supernovae explosions might obliterate a newly formed planet. The billion-year-old open cluster NGC 6811 is over 3,000 light years away and contains about 1,000 stars today (including several O-type stars and more than 100 B stars). At its birth, it probably contained some 6,000 stars. The glaring brilliance of the most massive stars in these clusters has long since burnt out, so Kepler was able to closely watch 377 fainter, longer-lived stars. So far, two of these stars turn out to host transiting planets. Two planets around 377 stars — Meibom and his colleagues wondered, was that rate normal? Or did the tightly-packed cluster stifle planet formation? If all the stars in NGC 6811 were field stars, Meibom’s team calculated that they would expect to find between 2 and 6 transiting planets and between 0.7 and 3.7 mini-Neptunes. (Of course, they’re not going to find partial planets, but these figures are based on a statistical study.) The two transiting mini-Neptunes Meibom’s team discovered fall squarely in the middle of the expected range. They calculated that between 0.1 and 2.3 Earth-sized planets and between 0 and 1.2 giant planets would be detectable — so the fact that the team didn’t find any Earth-sized or giant planets is also expected. “Whatever the process is that makes planets out of gas clouds, it works in the very dense regions of space where hundreds of stars are formed,” explains Kenneth Janes (Boston University). The existence of these two mini-Neptunes shows that planets can form just as well in neighborhoods far more crowded and violent than the calm environment of our Sun’s youth. Meibom plans to continue planet-hunting in even denser clusters until he finds the “crowdedness” threshold beyond which planets can’t form. Good question, Jeff. So far, only four other planets have been discovered in clusters (3 open, 1 globular). And each case is very different. The mini-Neptunes found in NGC 6811 orbit 1 billion year old G-type stars (let’s say expected lifetime about 10 billion years). The hot Jupiter in globular cluster M4 orbits dead stars (PSR B1620-26 and its white dwarf companion) but the planet is an estimated 13 billion years old. The planet found in the Hyades circled around the orange giant Epsilon Tauri (previously thought to be an A-type star). The two planets in the Beehive cluster were found orbitting late F and G dwarfs. This is a very interesting report Shari. Exoplanet fans are sure to welcome this news greatly, for it continues a trend in which planets are being found at more and more sites. This is proving that, just as star formation is a robust process, planetary formation must be as well. But Shari I’m having some difficulty with your fourth paragraph, wherein you wrote, “the Sun’s birthplace was 100 times less dense than NGC 6811, and the surrounding stars went their separate ways over several million years ago, maybe even before the stars and planets had finished forming.” First, how can we be so sure about the density of the Sun’s cluster? And secondly, since the Sun and its fellow cluster members are believed to have formed about 4.6 BYA from a loose cluster, wouldn’t their dispersion have happened far more than just “several million years ago”? Would there really be a hundred or more stars showing a disk? If many stars in the cluster were that close, I would not expect there to be any stable orbits. (Nor would I expect any planets to have formed. It would be kind of hot, too.) On the face of it, this is entirely unrealistic. If I’m correct, why did S&T publish this picture? 100% accuracy is neither possible nor required in a popular science magazine, but I think this falls well short of minimum. You are right,I misphrased that sentence, thank you for holding me accountable. It should read “the Sun’s birthplace was 100 times less dense than NGC 6811, and the surrounding stars went their separate ways over the course of several million years, maybe even before the stars and planets had finished forming.” Secondly, we are assuming that the Sun was born in a "typical" cluster, as we have no reason to believe otherwise at the moment. The following excerpt is from the paper: "For NGC6811 to have survived a billion years, the initial number density of stars in the cluster must have been at least that of the Orion Trapezium cluster (about 13,000 per cubic parsec) and thus more than two orders of magnitude greater than that of the typical cluster formed in a molecular cloud." Is it really likely that there are any O- and B-type stars left in a cluster with an estimated age of 1 billion years? I thought these stars had a lifetime of a couple of 100 million years max and should therefore have long "left the building"… All comments must follow the Sky & Telescope Terms of Use and will be moderated prior to posting. Please be civil in your comments. Sky & Telescope reserves the right to use the comments we receive, in whole or in part, and to use the commenter’s username, in any medium. See also the Terms of Use and Privacy Policy. Featured Observing Resources Sky and Telescope’s beloved Earth Globe is now available in a smaller 6-inch size! The detailed globe includes a freestanding base and information card filled with key features. Hold the whole world in your hands today!
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HIV and other viral infections are one leading cause of death. HIV is a disease in which a virus is replicated in the body which attacks the body's immune system. The HIV virus is not easily destroyed nor is there a good mechanism for keeping the host cells from replicating the virus. Herpes Simplex is another viral infection which is difficult, if not impossible, to cure. A method of treating these diseases and other viral infections is highly desirable. A material which targets the HIV virus and inhibit viral replication is highly desirable. Several drugs have been approved for treatment of this devastating disease, including azidovudine (AZT), didanosine (dideoxyinosine, ddI), d4T, zalcitabine (dideoxycytosine, ddC), nevirapine, lamivudine (epivir, 3TC), saquinavir (Invirase), ritonavir (Norvir), indinavir (Crixivan), and delavirdine (Rescriptor). See M. I. Johnston & D. F. Hoth, Science, 260(5112), 1286-1293 (1993) and D. D. Richman, Science, 272(5270), 1886-1888 (1996 An AIDS vaccine (Salk's vaccine) has been tested and several proteins which are chemokines from CD8 have been discovered to act as HIV suppressors. In addition to the above synthetic nucleoside analogs, proteins, and antibodies, several plants and substances derived from plants have been found to have in vitro anti-HIV activity. However, HIV virus is not easily destroyed nor is there a good mechanism for keeping the host cells from replicating the virus. Thus, medical professionals continue to search for drugs that can prevent HIV infections, treat HIV carriers to prevent them from progressing to full-blown deadly AIDS, and treat the AIDS patient. Herpes simplex virus (HSV) types 1 and 2 are persistent viruses that commonly infect humans; they cause a variety of troubling human diseases. HSV type 1 causes oral "fever blisters" (recurrent herpes labialis), and HSV type 2 causes genital herpes, which has become a major venereal disease in many parts of the world. No fully satisfactory treatment for genital herpes currently exists. In addition, although it is uncommon, HSV can also cause encephalitis, a life-threatening infection of the brain. (The Merck Manual, Holvey, Ed., 1972; Whitley, Herpes Simplex Viruses, In: Virology, 2nd Ed., Raven Press (1990)). A most serious HSV-caused disorder is dendritic keratitis, an eye infection that produces a branched lesion of the cornea, which can in turn lead to permanent scarring and loss of vision. Ocular infections with HSV are a major cause of blindness. HSV is also a virus which is difficult, if not impossible to cure. Hepatitis is a disease of the human liver. It is manifested with inflammation of the liver and is usually caused by viral infections and sometimes from toxic agents. Hepatitis may progress to liver cirrhosis, liver cancer, and eventually death. Several viruses such as hepatitis A, B, C, D, E and G are known to cause various types of viral hepatitis. Among them, HBV and HCV are the most serious. HBV is a DNA virus with avirion size of 42 nm. HCV is a RNA virus with a virion size of 30-60 nm. See D. S. Chen, J. Formos. Med. Assoc., 95(1), 6-12 (1996). Hepatitis C infects 4 to 5 times the number of people infected with HIV. Hepatitis C is difficult to treat and it is estimated that there are 500 million people infected with it worldwide (about 15 time those infected with HIV). No effective immunization is currently available, and hepatitis C can only be controlled by other preventive measures such as improvement in hygiene and sanitary conditions and interrupting the route of transmission. At present, the only acceptable treatment for chronic hepatitis C is interferon which requires at least six (6) months of treatment and or ribavarin which can inhibit viral replication in infected cells and also improve liver function in some people. Treatment with interferon with or without Ribavarin however has limited long term efficacy with a response rate about 25%. Hepatitis B virus infection lead to a wide spectrum of liver injury. Moreover, chronic hepatitis B infection has been linked to the subsequent development of hepatocellular carcinoma, a major cause of death. Current prevention of HBV infection is a hepatitis B vaccination which is therapeutically effective. However, vaccination is not effective in treating those already infected (i.e., carriers and patients). Many drugs have been used in treating chronic hepatitis B and none have been proven to be effective, except interferon. Treatment of HCV and HBV with interferon has limited success and has frequently been associated with adverse side effects such as fatigue, fever, chills, headache, myalgias, arthralgias, mild alopecia, psychiatric effects and associated disorders, autoimmune phenomena and associated disorders and thyroid dysfunction. Because the interferon therapy has limited efficacy and frequent adverse effects, a ore effective regimen is needed.
3.375
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Remote controls may be used for a variety of the purposes. For example, remote controls may be used to control televisions (e.g., high-definition televisions), monitors, MP3 players, audio receivers, radios, communication devices, personal computers, media players, digital video recorders (DVRs), game playing devices, set top boxes (STBs), security systems, household appliances, etc. Conventional remote controls may be configured to transmit data by sending transmissions (e.g., Radio Frequency (RF) transmissions, Infrared (IR) transmissions, etc.) which control the respective devices. Further, devices which are to be controlled by the transmissions from the remote control, may include, be electronically connected to or otherwise in communication with, receivers that receive the data transmissions from the remote control. Some conventional remote controls are designed such that upon a button of the remote control being pressed and held, a single transmission is transmitted. Other conventional remote controls are designed such that upon a button of the remote control being pressed and held, repeated transmissions are transmitted (e.g., transmissions may be repeated indefinitely or transmissions may be repeated for a limited amount of time to avoid draining the battery if, for example, someone is sitting on the remote control). Such a repeated transmission may be useful for commands such as volume control and channel changing. While these remote control features are beneficial, there remains an ever-present need for even more beneficial and even more convenient remote control functionality.
3.171875
3
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Power line communications (PLC) technology is aimed at transmitting digital data by utilizing the existing infrastructure of the electrical grid. It allows, in particular, remote reading of electric meters, exchanges between electric vehicles and the recharging terminals and also management and control of energy networks (smart grid). PLC technology incorporates, in particular, narrow band power line communication (N-PLC) which is generally defined as a communication over an electrical line operating at transmission frequencies of up to 500 KHz. N-PLC communication thus generally uses the frequency bands defined in particular by the European committee for electrotechnical standardization (CENELEC) or by the Federal Communications Commission (FCC). Thus, if the CENELEC A frequency band (3-95 kHz) is considered, the transmission frequencies are situated between 35.9375 and 90.625 KHz for the PLC-G3 standard. The overall performance of a receiver depends on the quality of its channel estimation, i.e. on the estimation of the transfer function of this channel. It is known that a transmission channel can vary in time, in frequency, in phase and in amplitude. Moreover, the signals conveyed by power line communications and received by the receiver result from a combination of several signals having followed within the transmission channel (i.e. the electrical line) several propagation routes or paths, each having its own time delay and its own attenuation (i.e. the transmission channel is a multi-path transmission channel). This may then result in strong attenuation of certain frequencies. Moreover, the properties and characteristics of the electrical networks are not known and may vary over time. Thus, the impedances of certain objects plugged in by the user vary with the voltage. Such is the case, for example, with halogen lamps or objects comprising voltage rectifiers. When a user plugs in such objects, it results in a periodic variation of the transfer function of the transmission channel. The channel is then considered to be linear and cyclostationary or “linear and varying temporally in a periodic manner”, this corresponding to the acronym LPTV (“Linear Periodically Time Varying”). Contemporary receivers, compatible with the PLC-G3 standard, are not suitable for performing channel estimations when the channel is time varying. Indeed, the PLC-G3 standard provides for the use of only two orthogonal frequency-division multiplexing (OFDM) symbols as pilot symbols to fully estimate the transfer function of the channel. Hence, when the channel varies, and in particular, when a cyclostationary channel is present, channel estimation may be erroneous, or perhaps impossible, and consequently potentially leads to errors in decoding the symbols.
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August 21, 2019 Clinical Contributors to this Story Cathie Ann Mancuso, M.D. contributes to topics such as Internal Medicine. Opal Thakar, M.D. contributes to topics such as Blood Pressure, Cardiac / Heart Health, Diabetes. Sapna Rama, D.O. contributes to topics such as Internal Medicine. A trend has swept across the country over the past few years: the use of electronic cigarettes, or “vaping.” Marketed as a healthier alternative to smoking cigarettes and with more than 7,000 flavors available, an increasing number of Americans—especially teens—are picking up the vaping habit. But is it really healthier than traditional smoking? The short answer: No. “While you may not be inhaling the tar associated with regular cigarettes, vaping introduces a new set of potentially damaging hazards,” says Sapna Rama, D.O., a board-certified internal medicine physician. “Certain ingredients in e-cigarettes can cause major damage to lung tissue. In addition to damaging lung tissue, e-cigarette devices have also been reported to cause burns, explosive injuries and chemical injuries.” The U.S. Surgeon General agrees, listing several ingredients and additives that could be harmful to your body: Ultrafine particles that you can inhale deep into your lungs Flavorants, like diacetyl, which can contribute to severe lung issues Heavy metals like tin, lead and nickel, which can cause poisoning Nicotine, the extremely addictive main ingredient that is linked to heart disease What Does the Research Say? While research is still being conducted on the effects of using e-cigarettes, several studies have shown troubling results. One 2016 study published in the journal Thorax showed that mice who had extended exposure to electronic cigarette vapor developed symptoms similar to COPD (chronic obstructive pulmonary disease). Another recent study from the Proceedings of the National Academy of Sciences showed that mice exposed to e-cigarette vapor had damaged DNA in the lungs, heart and bladder, which can potentially lead to the development of a variety of cancers. Other side effects include nosebleeds, irritability or loss of flavor perception. “There will be more research done in the future on the effects of e-cigarettes—but vaping is not healthier than smoking,” says Opal Thakar, M.D., a board-certified family medicine physician. “But in the meantime, we know already that smoking of any kind is detrimental to your health.” How to Quit Fortunately, there are safe ways to help you stop smoking both cigarettes and e-cigarettes. These include prescription nicotine inhalers or nasal sprays and over-the-counter options like nicotine patches, gum or lozenges. Because nicotine has its own deleterious effects, your doctor can help slowly reduce your intake until you are off nicotine for good. There are also non-nicotine medications that can be prescribed, like Zyban or Chantix. Cathie-Ann Mancuso, M.D., a board-certified internal medicine physician, says to talk openly with your doctor to find the best options for you. “Obviously, it would be ideal to stop using nicotine altogether, but stopping ‘cold turkey’ isn’t for everyone,” says Dr. Mancuso. “Rest assured that there are plenty of replacement aids and helpful resources available to you.” Other effective techniques to try while quitting include: Exercising or performing a physical activity every time you get an urge to smoke Delaying your response to cravings. Tell yourself to wait 10 minutes and find an engaging activity to distract your brain. Practicing yoga or meditation to help relax Talking to professionals or attend group sessions with others who are quitting Next Steps & Resources: The material provided through HealthU is intended to be used as general information only and should not replace the advice of your physician. Always consult your physician for individual care.
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For the first time, researchers have succeeded in levitating and moving arbitrarily shaped objects using acoustic (sound) waves. The researchers, from the Swiss Federal Institute of Technology (ETH) in Zurich, have already used their new-found magical powers of levitation to collide a granule of coffee and water to create instant coffee in midair — and more excitingly, a droplet of water and a piece of sodium (the explosively awesome video is embedded below). The same approach could potentially work on humans, though, without further refinements to the technology, we would probably explode or suffer catastrophic internal bleeding. Acoustic levitation is desirable because, unlike magnetic levitation, it can be used on any object — not just materials and liquids that are magnetic. Likewise, buoyancy can be used to “levitate” some liquids, but again there are strict limitations on what liquids can be used (they must be immiscible, as with water and oil). The only limitation with acoustic levitation is that the object’s diameter must correspond to half the wavelength of the acoustic waves. As you can see, the team have no issues levitating a toothpick — something that would be impossible with both magnetic and buoyancy levitation. Acoustic levitation has been performed before, but with very limited control of the object’s movement (video below). The breakthrough here is that researchers are able to move their acoustically levitated objects up and down, as well as side to side. The levitation effect is created by standing waves — static (standing) waves that are held in place by a reflector that bounces the same wave back upon itself, causing interference. Whereas waves usually oscillate up and down as they move through the air, a standing wave is essentially static, with the waveform forced to stay in one place. This standing wave creates a consistent upwards pressure that, if it has a strong enough amplitude (volume), can cancel out the gravity of an object placed in the standing wave. In short, if you have enough power, you could levitate just about anything with acoustic waves — including a human. The power required would be immense, though, and at this point it isn’t clear if a human would even survive the acoustic forces. Furthermore, before you start dreaming of a portable levitation device (a jet pack!), the power requirements would probably be well beyond the capabilities of today’s lithium-ion battery packs. (Levitating a water drop requires around 160 dB). In reality, this new development — being able to levitate multiple objects and manipulate them in a 3D space — is much more likely to find use on a smaller scale. There are many chemical and biological processes that can be disrupted by contact with a surface, and acoustic levitation is the perfect solution for such situations. Not being confined to magnetism or buoyancy as a means of levitation is also a massive boon for science: Instead of being confined to purely magnetic objects, scientists can now react anything with levitation. This might be as straight forward as reacting water and sodium, as per the video above, or it might be as complex as introducing foreign DNA into other cells using DNA transfection. Now read: MIT discovers a new state of matter, a new kind of magnetism Research paper: doi: 10.1073/pnas.1301860110 – “Acoustophoretic contactless transport and handling of matter in air”
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The effect of skin reflectance on thermal traits in a small heliothermic ectotherm. Variation in colour patterning is prevalent among and within species. A number of theories have been proposed in explaining its evolution. Because solar radiation interacts with the pigmentation of the integument causing light to either be reflected or absorbed into the body, thermoregulation has been considered to be a primary selective agent, particularly among ectotherms. Accordingly, the colour-mediated thermoregulatory hypothesis states that darker individuals will heat faster and reach higher thermal equilibria while paler individuals will have the opposite traits. It was further predicted that dark colouration would promote slower cooling rates and higher thermal performance temperatures. To test these hypotheses we quantified the reflectance, selected body temperatures, performance optima, as well as heating and cooling rates of an ectothermic vertebrate, Lampropholis delicata. Our results indicated that colour had no influence on thermal physiology, as all thermal traits were uncorrelated with reflectance. We suggest that crypsis may instead be the stronger selective agent as it may have a more direct impact on fitness. Our study has improved our knowledge of the functional differences among individuals with different colour patterns, and the evolutionary significance of morphological variation within species.
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Introduction {#S0001} ============ Intestinal helminthic infections are important public health problems in developing countries \[[@CIT0001]\]. They are the most common infections among school age children and they tend to occur in high intensity in this age group \[[@CIT0002]\]. The World Health Organization estimates that over 270 million pre-school children and over 600 million of school children are living in areas where the parasites are intensively transmitted and are in need of treatment and preventive interventions \[[@CIT0003]\]. These infections are most prevalent in tropical and subtropical regions of the developing world where adequate water and sanitation facilities are lacking \[[@CIT0004]\]. The global prevalence and number of cases of intestinal helminths infection in school age children have been estimated to be Roundworm 35% (320 millions); Whipworm 25% (233 millions); Hookworm 26% (239 millions), others 14% (128millions) \[[@CIT0005]\]. Other species of intestinal helminths are not widely prevalent. Intestinal helminths rarely cause death. Instead, the burden of disease is related to less mortality than to the chronic and insidious effects on health and nutritional status of the host \[[@CIT0006], [@CIT0007]\]. In addition to their health effects, intestinal helminth infections also impair physical and mental growth of children, thwart educational achievement, and hinder economic development \[[@CIT0008], [@CIT0009]\]. The high prevalence of these infections is closely correlated with poverty, poor environmental hygiene and impoverished health services \[[@CIT0010]\]. Intestinal helminth infections occur in all regions of Africa; particularly in sub-Saharan Africa, they are common and of major health concerns because of factors that predispose man to the infections such as poverty, poor sanitation, ignorance and malnutrition prevail \[[@CIT0011]\]. In Ethiopia, intestinal parasitic infections are highly prevalent because of low living standards, poor environmental sanitation, unsafe human waste disposal systems, inadequacy and lack of safe water supply, and low socio-economic status \[[@CIT0012]\]. Report from a literature survey indicated that Ethiopia has one of the lowest quality drinking water supply and latrine coverage in the world \[[@CIT0013]\]. This could be one reason for why intestinal parasitism has been widespread in Ethiopia. Moreover, parasitic helminthic infections are the second most predominant causes of outpatient morbidity in the country \[[@CIT0012]\]. In Ethiopia the prevalence of *Ascaris lumbricoides* infection was 29% in the highlands, 35% in the temperate areas and 38% in the lowlands. The prevalence of hookworm infection was highest in the lowlands (24%) followed by the temperate (15%) and highland (7%); whereas *Trichuris trichiura* infection exhibited similar prevalence\'s in all altitudinal regions (13% on the average) \[[@CIT0014]\]. So far several studies identifying the prevalence of intestinal parasites in general and the prevalence of intestinal helminths in particular have been carried out in Ethiopia \[[@CIT0015]--[@CIT0019]\]. Conducting a survey on the prevalence of various intestinal helminthic infections in different geographic regions is a prerequisite for developing appropriate control strategies. Hence, the World Health Organization (WHO) presented a simple methodology to assess the prevalence of helminths, stratified by ecozones, for settings where information is scarce \[[@CIT0020]\]. Data from a study in Nigeria indicated that intestinal helminthiasis differs by sex of school children \[[@CIT0021]\]. In contrast, a similar study in Gondar has shown; intestinal helminthiasis did not differ by sex of school children \[[@CIT0017]\]. Previous study in Babile town reported an overall prevalence of intestinal helminthiasis to be 27.2% and the predominant species identified being *Hymenolepis nana* with a prevalence rate of 10.1% \[[@CIT0022]\]. In spite of the fact that a number of studies have been undertaken over the years on the prevalence of intestinal helminths among school children in different part of Ethiopia, yet there are several areas in all the regional states from which epidemiological information is lacking including our study area, Babile town. Therefore, this study is aimed at determining the prevalence of intestinal helminthic infections among elementary students of Babile town. It is believed that this study will provide recent information for those who are working in the prevention and control of intestinal helminthiasis. Methods {#S0002} ======= This study was conducted in Babile town, Eastern Hararghe from May 14 to June 8, 2012. The town is located about 561 Km away from the capital, Addis Ababa. It is situated in eastern Hararghe Zone between two nearby towns named: Harar and Jigjiga. The total population of the town are 17, 704 of which 8782 are males and 8922 are females. Babile town is situated at an altitude of 1340 meters above sea level with mean annual rainfall and mean annual temperature of 410 -- 800mm and 24°C -- 28°C respectively. In the town there are two elementary schools (Babile Elementary School \#1 & Babile Elementary School \#2) and one secondary school. In the town there are 3742 students of which 2086 are males and 1656 are females. The heath coverage of the town reached almost 100%. The water and latrine coverage of the town were 28% and 90% respectively \[[@CIT0023]\]. Six hundred forty four students were selected from the schools to participate in the study and the sample size was determined using the standard formula for single population proportion & the proportion of STHs among elementary students of Babile town was 14.2% (p = 0.142) \[[@CIT0022]\] to get maximum sample size, expected margin of error set at 4% (d = 0.04) and with 95% confidence level. Hence, the calculated sample size becomes 644. Then, the sample size was allocated to the two elementary schools proportional to size and the sampling frame was the students' enrollment list from the two schools. Hence according to probability proportional to size calculation Elementary school No 1 contributed 567 students of the 644 sample size and Elementary school No 2 contributed 77 of the 644 required sample size. Then the study subjects were selected from the list at random using random number table i.e. 567 students from the enrollment list of Elementary school No 1 and 77 students from the enrollment list of Elementary school No 2. All the selected 644 students were voluntary to participate in the study and hence received an interview after providing the stool sample. This makes the response rate to be 100%. All the necessary information was collected using pre-structured questionnaire. Two Technicians from the local health center were recruited and assigned as data collectors. School teachers and unit leaders helped the data collectors in the entire data collection process. All the time before beginning stool sample collection, the latrines were inspected for cleanliness by the data collectors to get them cleaned. After giving adequate instruction on how to collect the stool sample, each study subject was provided a stool cup and applicator stick to bring at least 3gm of fresh stool sample of his/her own, that was sufficient for egg count by the McMaster method to determine the prevalence and infection intensity of soil transmitted helminths and the prevalence of other helminthic parasites. Unit leaders of the two schools attended students who are small enough for proper stool sample collection. A laboratory Technologist supervised the appropriateness of the stool sample delivered by the study participants before accepting as a sample. After providing the required stool sample, all the students were interviewed by the data collectors for the completion of data collection. Finally each sample was labeled and transported (after being preserved using formalin) to Harar Campus side lab together with filled questionnaire for processing and examination. All collected stool samples were processed by the McMaster Method for egg count to determine the prevalence and infection intensity of soil transmitted helminths and to determine the prevalence of other intestinal helminths \[[@CIT0024]\]. The generated data were entered, cleaned and analyzed using SPSS version 16.0. Intestinal helminth prevalence was expressed as the percentage of subjects found positive for each helminth. Univariate analysis was carried out using the Chi-square test to check for presence or absence of association between each exposure and the presence of infection and odds ratios with 95% CI were computed to measure the strength of association. Logistic regression was used to calculate predictors of helminthic infection. Statistical significance was set at P \< 0.05. Ethical clearance was obtained from Institutional Research Ethics Review Committee (IRERC), College of Health and Medical Sciences, Harar campus, Haramaya University. Informed written consent from the parents of each student and verbal ascent from the students were obtained before data collection. The objective and benefit of the study was thoroughly explained to the Parents/Guardians/Teachers of the study subjects. Only volunteers were involved and students were having the right to withdraw from the study. Information meeting was held with parents/guardians/school teachers and with the students to explain the purpose of the study, and the procedure involved. Results were kept confidential. All students positive for *Hymenolepis nana* were treated with Praziquantel at a dose of 25mg/kg and those students positive for *Trichuris trichiura, Enterobius vermicularis* and hookworms were treated with Mebendazole at a dose of 100mg for three days. Results {#S0003} ======= Socio-demographic characteristics {#S20004} --------------------------------- A total of 644 students from the two elementary schools of Babile town were participated in this study. Of the 644 stool specimens examined 89 were positive for one or more intestinal helminths making the prevalence rate 13.8%. Out of the 644 study participants 364 (56.5%) were males and 280 (43.5%) were females. The age range of the students varies between 5 and 25. Of which age range 5 -- 14 years consists of the highest number of students 593 (92.1%) the remaining 51 (7.9%) students were found in the age range 15 -- 25 ([Table 1](#T0001){ref-type="table"}). Mean age of the students was 10.45 years + 2.9 SD. The weight of the students varies between 15kg and 70 kg with mean weight of 31.84 kg + 10.15SD. Similarly the height of the students varies between 1.04m and 1.80m with mean height of 1.38m + 14.43SD. ###### Socio-demographic characteristics of students in Babile town, Eastern Ethiopia, 2012 Variables Frequencies (n = 644) \% ------------ ----------------------- ------ ------ Sex Male 364 56.5 Female 280 43.5 Age group 5-14 593 92.1 15-25 51 7.9 Ethnicity Oromo 352 54.7 Somali 165 25.6 Amhara 101 15.7 Gurage 24 3.7 Harari 1 0.2 Tigray 1 0.2 Religion Muslim 515 80.0 Orthodox 99 15.4 Protestant 30 4.7 Prevalence of intestinal helminths {#S20005} ---------------------------------- The prevalence of intestinal helminths was 13.8% (89 out of 644). The most prevalent detected parasite was *Hymenolepis nana* 13% (84/644) followed by *Enterobius vermicularis* 0.6% (4/644) and the by Hookworms 0.3% (2/644). The least prevalent was *Trichuris trichiura* 0.2% (1/644). Furthermore, the prevalence of soil transmitted helminths was 0.47% (3/644). Both hookworm infected students were with light infection intensity (100 eggs per gram of feces and 200 eggs per gram of feces respectively). Similarly *Trichuris trichiura* infected student was with light infection intensity (300 eggs per gram of feces). Risk factor analysis for intestinal helminthic infections {#S20006} --------------------------------------------------------- Out of the 89 positive students for intestinal helminths 41 were males and the remaining 48 were females. There is a statistical significant intestinal helminth infection difference between males and females (OR 0.61 and 95% CI is 0.39 -- 0.96) and (P = 0.033) ([Table 2](#T0002){ref-type="table"}). Out of the 89 intestinal helminthiasis infected students, 85 were found in the age range 5-14, four were in the age range 15-25. Intestinal helminthiasis infection is independent of age range of students (cruds OR 1.97 and 95% CI is 0.69 -- 5.60) (P = 0.205) ([Table 2](#T0002){ref-type="table"}). Of 89 infected students, only 2 (2.2%) students were infected with two parasites i.e. by *Enterobius vermicularis and Hymenolepis nana*. The remaining 87 (97.8%) were infected with one parasite only. Out of the 89 intestinal helmiths infected students, 26 (16.7%), 18 (17.5%), 15 (17.2%), 19 (19.6%), 3 (5.1%), 4 (7.5%), 2 (5.3%), and 2 (3.9%) students were from grades 1, 2, 3, 4, 5, 6, 7, and 8 respectively. A statistically significant intestinal helminthic infection difference was observed among the different grades (P = 0.018) Six hundred forty four students from the two elementary schools participated in this study. Of which 443 (68.8%) were first cycle students (Grades 1 - 4) and the remaining 201 (31.2%) were second cycle students (Grades 5 - 8). Out of the 89 intestinal helmiths infected students, 78 (17.6%) were first cycle students and the rest 11 (5.5%) were second cycle students. A statistically significant intestinal helmithic infection difference was observed between first and second cycle students (OR 3.70 and 95% CI is 0.69 -- 5.60) (P = 0.205) (P = 0.001) ([Table 2](#T0002){ref-type="table"}). All the other risk factors such as parents' occupation, family size, finger nail status, shoe wearing habit, presence or absence of latrine, and water source for drinking were not associated with intestinal helminthiasis (P \> 0.05). ###### Univariate risk factor analysis for intestinal helminthic infection among students of Babile town, Eastern Ethiopia, 2012 Variables Result of stool examination OR(95% CI) P-value ------------------- ----------------------------- ---------------------------- ------------------- ------- **Sex** Male 323(88.7%) 41(11.3%) 0.61(0.39, 0.96) 0.033 Female 232(82.9%) 48(17.1%) 1 **Negative for Helminths** **Positive for Helminths** **Age range** 5 - 14 508 (85.7%) 85 (14.3%) 1.97 (0.69, 5.60) 0.205 15 - 25 47 (92.2%) 4 (7.8%) 1 **Negative for Helminths** **Positive for Helminths** **Grouped grade** First cycle 365 (82.4%) 78 (17.6%) 3.70 (1.92, 7.12) 0.001 Second cycle 190 (94.5%) 11 (5.5%) 1 After adjusting for all predictors of helminthic infection, females were two times more likely to develop intestinal helminthic infection than males (Adjusted OR 1.67 and 95% C.I. is 1.04 -- 2.67) (P = 0.033). Similarly, students of lower grade were four times more likely to develop helminthic infection than students of higher grade (Adjusted OR 3.75 and 95% C.I. is 1.65 -- 8.55) and (P = 0.002) ([Table 3](#T0003){ref-type="table"}). ###### Parameter estimates from multivariable logistic regression model predicting the probability of helminthic infection among students of Babile town, Eastern Ethiopia, 2012 Predictors of helminthic infection B P-Value Adjusted OR 95.0% C.I. ------------------------------------- ------- ----------------------------------------- ------------- ------------ ------- Sex (Male) 1.00 Sex 0.51 0.033[\*](#TF0001){ref-type="table-fn"} 1.67 1.04 2.67 Age (Years) -0.02 0.710 0.98 0.88 1.09 Grade of students (Second cycle) 1.00 Grade of students 1.32 0.002[\*](#TF0001){ref-type="table-fn"} 3.75 1.65 8.55 Finger nail status (Trimmed) 1.00 Finger nail status -0.59 0.354 0.56 0.16 1.93 Latrine usage (Always) 1.00 Latrine usage 0.50 .668 1.64 0.17 15.86 Hand washing after defecation (Yes) 1.00 Hand washing after defecation -0.51 0.666 0.60 0.06 6.02 Eating uncooked vegetables (No) 1.00 Eating uncooked vegetables 0.26 0.707 1.30 0.33 5.07 Water for drinking (Tap water) 1.00 Water for drinking 0.19 0.574 1.21 0.627 2.32 P-value significant at \<0.05 Discussion {#S0007} ========== Helminths are the most common infectious agents of humans in developing countries and produce a global burden of disease that exceeds better-known conditions, including malaria and tuberculosis \[[@CIT0025]\]. The inhabitants of thousands of rural, impoverished villages throughout the tropics and subtropics are often chronically infected with several different species of parasitic worms \[[@CIT0026], [@CIT0027]\]. For reasons not well understood, compared with any other age group, school-aged children (including adolescents) and preschool children tend to harbor the greatest numbers of intestinal worms \[[@CIT0028]\]. Despite the fact mentioned above the prevalence rate of intestinal helminthiasis in present study was 13.8% the majority being mono-infection. This was happened due to the regular de-worming of schoolchildren that had already been started by the local Health Bureau (Personal Communication). The concerned health professionals of the Bureau is undertaking the de-worming campaign regularly every six month using a single day dose of 400mg Albendazole during the school days in collaboration with teachers, unit leaders and Directors of the two schools. It may also be due to the improved health service coverage by the local Health Buearu \[[@CIT0023]\]. In the present study an overall prevalence of 13.8% intestinal helminthic infection was found. This finding was lower when compared with previous study conducted in the same area 11 years ago 27.2% \[[@CIT0022]\]. This difference could be explained by the increased involvement of College of Health and Medical Sciences, Haramaya University through its normal teaching learning processes i.e. students assigned for Team Training Program (TTP) for the last many years might have contributed to the improvement of the health status of the community in the study area through time in addition to the de-worming campaign introduced in the area. It is also in disagreement with previous studies in Ethiopia; 26.9% among school children of community school at University of Gondar \[[@CIT0017]\], and 47.1% among school children of Jimma zone \[[@CIT0019]\]. The possible explanation for this difference could be better climatic and geographic condition of Babile town than Jimma and Gondar areas that prohibits the transmission of intestinal helminths. In this study the prevalence of soil transmitted helminths was 0.47%; which was very much lower in comparison to different previous studies conducted in Ethiopia such as 14.2% in Babile \[[@CIT0022]\], 38.4% in Jimma zone \[[@CIT0019]\], 43.3% in Zarima, Gondar \[[@CIT0018]\], 63% in Chencha, Southern Ethiopia (Ashenafi), and 66.5% in Delgi, Gondar \[[@CIT0015]\]. This low prevalence could be due to the increased health service coverage by the local health Buearu in addition to the launching of periodic de-worming program by the Ethiopian government. The predominant parasite detected in this study was H. nana with a rate of 13% which is almost similar to the study conducted among school children of Community school at the University of Gondar 13.8% \[[@CIT0017]\]. However, it was slightly higher than the study conducted in the same area some 11 years ago with a rate of 10.1% \[[@CIT0022]\]. This is may be associated with the life cycle of the parasite; it is one the auto-infecting helminths that can be transmitted by autoinfection means if and only if remained untreated. This finding revealed that despite periodic de-worming the prevalence of *H. nana* is on increase. This is because the de-worming focuses primarily on soil transmitted helminths by the known anthelminthic Albendazole which has little effect on eliminating *H. nana* on a single day dose administration. This increment in prevalence rate of *H. nana* shows absence of concern towards hymenolepiasis by the responsible bodies. This is an indication for the need to do further investigation on hymenolepiasis with its determinant factors for a plausible solution to be forwarded. The observed 13% prevalence of Hymenolepiasis is in contrast with previous reports from different regions of Ethiopia; 0.8% in Chencha, Southern Ethiopia \[[@CIT0016]\], 2.1% in Jimma zone \[[@CIT0019]\], and 6.8% in Delgi, Gondar \[[@CIT0015]\]. This difference may be explained by variations in socio-economic status, climatic and geographic condition of the study area as well as local endemicity of the study area for this particular parasite. In our study univariate analyses indicated that more female children 48 (17.1%) were infected with intestinal helminths than male children 41(11.3%) and found to be statistically significant (P = 0.033) ([Table 2](#T0002){ref-type="table"}). This is in agreement with data obtained from a study in Nigeria; reported as female children (56.6%) were more infected than male children (46.4%) and the difference was statistically significant (P = 0.0019) \[[@CIT0021]\]. However, it is in disagreement with Gondar\'s study reported that no statistical significant association was observed between males and females (p = 0.301) \[[@CIT0017]\]. Higher helminthic infections were observed among the age range 5 -- 14 compared to the age range 15 -- 25 in the present study although the difference was not statistically significant (P = 0.205) ([Table 2](#T0002){ref-type="table"}). In the present study, a strong association between intestinal helminths and grades of students was detected (P = 0.018). That is, the lesser the grades of the students the more will be the intestinal parasites seen. This study also revealed that the existence of an overall intestinal helminthic infection difference between first and second cycle students (P = 0.001). This is in accordance with a previous report in Gondar town indicating that Children in grade one to grade three had a higher prevalence of intestinal helminthic infections than those in grades four to eight (p = 0.031) \[[@CIT0017]\]. Of all the predictors of intestinal helminthic infection, sex is significantly associated with intestinal helminthic infection. Because logistic regression analysis showed that females are two times more likely to develop intestinal helminthic infection than males (Table-3). This could be due to carelessness and unhygienic habits practiced by female children than male children in Babile town. Similarly, of all the predictors of intestinal helminthic infection, grade of the students is significantly associated with overall intestinal helminthic infection. Because logistic regression analysis showed that students of lower grade are four times more likely to develop intestinal helminthic infection than students of higher grade. This could be speculated by increase in awareness; as grade increases awareness increases so that students of higher grade will have less exposure to intestinal helminthic infection than students of lower grade ([Table 3](#T0003){ref-type="table"}). Because students of higher grade are the more mature age group with a higher level of personal hygiene in contrast to students of lower grade. Conclusion {#S0008} ========== The current study identifies low prevalence of intestinal helminthiasis. Nearly one out of ten students was infected with intestinal helminths; almost all with *Hymenolepis nana*. Extremely low number of students almost one out of two hundred was infected with soil transmitted helminths. Female children are two times more likely to develop intestinal helminthic infection than male children. Students of lower grade are four times more likely to develop intestinal helminthic infection than students of higher grade. Generally health information dissemination is suggested to be given to students on how to protect themselves from intestinal helminthic infections with special emphasis for female children. It is also suggested that the local Education Bureau as well as the local Health Bureau need to provide safe learning environment especially for students of lower grade such as school sanitation. Since infection by *Hymenolepis nana* is a long term health problem in the area, provision of regular treatment to students of the town by anthelminthic drug of choice against hymenolepiasis is also recommended. This study was financially supported by Haramaya University government fund. We would like to thank M/rs. Zuhera Shafi, M/rs. Ayantu Gerba M/rs. Serawit Tamrat and M/rs. Meskerem Yeshitla for their unreserved support during data collection and sample processing. We are greatful to S/r Firehiwot for her helpfulness in assisting us in some part of data analysis. We also thank directors, Unit Leaders and Teachers of the two Elementary schools of Babile town. Competing interests {#S0009} =================== The authors declare that they have no competing interests. Authors' contributions {#S0010} ====================== Ephrem Tefera conceived the study and drafted the proposal, carried out data collection, laboratory examination, data analysis and interpretation of the results, ultimately finalized write up of the manuscript. Jemal Mohammed assisted in proposal preparation, carried out data collection, and laboratory examination. Habtamu Mitiku carried out data collection, laboratory examination and analysis of data. All authors read and approved the final manuscript.
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3
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[Adaptive significance of the ciradian rhythm of oviposition in Drosophilidae: comparison of eight species of the genus Zaprionus]. The circadian rhythm of oviposition under light conditions LD 12:12 was studied in eight species of Zaprionus. Interspecific differences proved to be of little importance. In all cases, the maximum of egg production took place at the beginning of the photophase and egg laying was often restricted to a few hours. Such a rhythm is highly different from that observed, in a previous work, among the Drosophila species of the melanogaster subgroup.
3.015625
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Introduction {#Sec1} ============ With the development of modern science and technology, huge quantities of chemicals are used, and more than 15 million chemicals are sold worldwide \[[@CR1]\]. Humans routinely use chemicals and can be exposed to them in everyday accidents. Although they are widely used, the impact of many chemicals on human health is still unknown. With increasing concern about the safety of chemicals, human exposure has emerged as an important issue such as humidifier disinfectants. Given the widespread use of chemicals, there are many risks associated with chemical accidents and diseases. Chemical incidents reported worldwide between 1970 and 1998 resulted in leaks, fires, and explosions involving more than 100,000 casualties \[[@CR2], [@CR3]\]. Since chemicals are stored in huge quantities, the magnitude and extent of damage when a chemical accident occurs can be significant \[[@CR2]\]. In the 2007 "Toxicity test for the twenty-first century: Vision and strategy," the National Research Council (NRC) planned a new toxicity test system to describe a new paradigm shift in the assessment of the hazards and risks of chemicals, via a new computational biological test method used to study toxic pathways for the expansion of in vitro testing \[[@CR4]\]. In this context, the "adverse outcome pathway (AOP)" is a biological pathway that disturbs homeostasis, which causes toxicity. The description of toxicity begins with chemical characterization and explains the interaction between them. Target tests to identify impacts at critical stages of the pathway and dose--response extrapolation to estimate human exposure are required. Predicting ecosystem impacts requires additional population-based modeling. This is a conceptual framework for organizing existing biological information, and AOP consists of molecular initiative event (MIE), key events (KEs), and adverse outcome (AO). This independent element represents a biological response and is associated with major event relationships. The AOP concept provides instinctive risk identification to help assess the carcinogenicity of chemicals. This highlights the application of the AOP concept and the effective application of cancer prevention by predicting the carcinogenicity of chemicals \[[@CR5]\]. Results {#Sec3} ======= Concept and role in chemical hazard assessment {#Sec4} ---------------------------------------------- Molecular initiative event (MIE) is the initial point of the AOP and represents chemical interactions at the molecular level, such as ligand--receptor binding or DNA binding. Key event (KE) is a biological change caused by a molecular initiative event at various levels, such as cells and tissues. An adverse outcome (AO) is a particular type of KE, representing an endpoint of biological disturbances due to MIE. Molecular initiative event, key event, and AO are connected by a unidirectional arrow called key event relationship (KER), which means predictive interaction between upper and lower KE, making it easy to estimate the state of each KE \[[@CR6]\]. Each factor in the AOP must be based on the weight of evidence (WoE) that meets the Bradford Hill criteria. Establishing the mode of action (MoA) hypothesis is based on causality criteria, considerations of coherence, specificity of relationships, coherent time relationships, dose--response relationships, biological validity, coherence of evidence, and alternative explanations \[[@CR7]--[@CR9]\]. The WoE is the concept of providing evidence that meets information requirements using information from independent sources \[[@CR10]\]. One AOP should have one MIE and one AO, but there is no limit to the number of intermediate KEs, and each KE can be included in a different AOP. Adverse outcome pathways describe the sequence of causality in biological responses to chemicals at various levels \[[@CR11]--[@CR13]\]. Any type of information related to a biological response (e.g., in vivo and in vitro test results, electronic data, biomarkers, etc.) may be applied to the AOP \[[@CR8]\]. Thus, AOP is a dynamic technology that allows existing information to be more accurately changed as the technology used to monitor biological responses evolves \[[@CR14]\]. Because AOP is expressed in a simple flowchart, it is easy to instinctively understand the side effects of chemicals, and the concept of AOP is not a sudden occurrence, but an evolution of existing concepts related to toxic mechanisms \[[@CR11], [@CR15]\]. Mode of action (MoA) frameworks {#Sec5} ------------------------------- The carcinogen mode of action (MoA) framework of early International Program on Chemical Safety (IPCS) oversees the systematic process of describing the chemical early international programs on chemical MoA in animals and determines relevance in humans through comparisons. Early IPCS techniques set out some basic principles of pathway-based techniques, and MoA is defined as a series of key events along biological pathways from initial chemical interactions to toxicological consequences. One MoA was studied at a time, recognizing that MoA does not have to be complete to be useful; a chemical can have more than one MoA and may therefore be associated with multiple possibilities, each of which can be critical to toxicity studies. To establish a model for defining "key events" as possible pathway steps and to systematically establish causal relationships between key events, the MoA must ensure the importance of setting quantitative parameters. In this regard, the MoA is distinguished from the mechanism of action, the latter being a more detailed description of pathways involving molecular interactions \[[@CR16]\]. The MoA has generally been updated to accommodate insights into the pathway-based approach to risk assessment, where MoA and AOP are conceptually similar, but MoA does not necessarily imply toxic expression (e.g., effect as drugs) \[[@CR16]\]. Over the last decade, attempts to describe and predict the biological and toxicological effects of chemicals have gradually shifted to the consideration of mechanized automation. Of the many reports in the burgeoning field of predictive toxicology, the US NRC's "21st Century Toxicity Testing: Vision and Strategy" attracted considerable attention and discussed the need for a paradigm shift in the assessment of the hazards and risks of chemicals \[[@CR4], [@CR11], [@CR17]--[@CR21]\]. The NRC report plans to change the current way of conducting toxicological tests, which are based on animal phenotypes, with techniques that are increasingly dependent on understanding the molecular mechanisms of toxicity in human cells and tissues. The transition to more mechanistic hazard assessment is the "high-throughput screening (HTS) and high-content screening (HCS)" in mammalian (especially human) cell lines and/or tissue cultures. This implies the use of in vitro tests based on various calculations for data analysis and interactions between toxicity and molecular targets, side effects, and outcomes. The general premise of AOP technology means that there are sufficient events to explain biological pathways and to predict toxic pathways at different levels of biological tissue (cells, tissues/organs, organisms, populations). A basic understanding of molecular interactions and effects should be able to predict the side effects of organisms and populations. Adverse outcome pathway technique {#Sec6} --------------------------------- The AOP technique was initiated in the field of ecological toxicology as a way to address the uncertainty of hazard assessments for an increasingly diverse environment, and as reported by Ankley et al. \[[@CR11]\] adverse outcome pathway is a "causal, mechanical, inferential, or correlated relationship." It is a flexible technology that can include infrastructure-based connections, and the information on which they are based can include both mechanisms and MoA in vitro, in vivo, or computational systems. Adverse outcome pathway describes an MIE that occurs at the onset of chemical exposure, beginning with the interaction between the biomolecule (e.g., proteins, receptors, etc.) and the molecule and subsequently health in cells and in humans. All types of information can be integrated from the molecular level to the individual level to predict hazard consequences and provide biological arguments (or a set of hypotheses), including individual toxicity levels for hazards or environmental hazards. The Organization for Economic Co-operation and Development (OECD), the US Environmental Protection Agency (EPA), and the European Commission (EC) joint research centers have developed a chemical knowledge-based toxicity pathway (AOP-KB), and the AOP-KB has attracted the interest and participation of stakeholders, including government, academia, and industry, in that it provides a point of contact with academic research achievements that can be directly linked to government chemical regulation. The concept of AOP is useful for developing predictive toxicity tools, and even short-term imperfect AOPs can show the relationship between chemicals and risk. The certainty of interpretation between existing and new information can be increased, and it can be used as an integrated test strategy to maximize that certainty \[[@CR22]\]. Recent trends in adverse outcome pathways {#Sec7} ----------------------------------------- The concept of AOP was first announced in 2010 by Ankley et al. \[[@CR11]\] with 243 AOPs and 1800 KEs registered and developing as of August 2018. This AOP information is available free of charge in the AOP-KB, the leading AOP database maintained by the OECD; the site has been published by the US EPA to share and discuss relevant information among AOP developers. The project began in collaboration with EC's joint research center and the US army technician R&D center \[[@CR23]\]. Knowledge-based adverse outcome pathway (AOP-KB) consists of AOP-Wiki, Effectopedia, Intermediate Effects DB, and Xplorer \[[@CR24]\]. AOP-Wiki provides a system that organizes the available knowledge and published research information concerning AOP, KE, KER, and stressors, respectively. Effectopedia is a modeling platform that is designed for the development and application of AOP. Experimental data are used to provide quantitative information about the AOP component, and a beta version of Effectopedia is currently available. Medium impact DB processes chemical information and describes how chemicals cause MIE or KE. AOP Xplorer is a calculation tool for mapping AOP. Intermediate DB and AOP Xplorer are currently in development, and all four systems share information through the AOP-KB hub. Since each element of AOP-KB is individually arranged, AOP-KB is useful for the development of AOP and is applied from various studies \[[@CR13]\]. The OECD provides comprehensive management of AOP development and evaluation \[[@CR6]\] and is overseen by the OECD extended advisory group on molecular screening and toxicogenomics (EAGMST). The AOP-Wiki is administered by the Toxic Pathology Society, in accordance with the OECD extended advisory group on molecular screening and toxicogenomics guidelines \[[@CR23]\]. Since the OECD published its first AOP, "Skin sensitization pathways initiated by covalent bonds to proteins," several reports and guidance on AOP have been published, and the OECD provides eight AOP-related publications. As of August 2018, the AOP development program workbook lists 60 projects \[[@CR24]\]. AOPs for chemicals in workplace {#Sec8} ------------------------------- Respiratory sensitivity is an important occupational health issue for workers, and understanding the mechanistic basis for this effect is necessary to support the development of toxicological tools to detect the chemicals. Recently, AOP systems and techniques have been used to organize the information to better convey the understanding of chemical respiratory sensitization, which is similar to AOP for skin sensitization, but with specific differences. The composition of these AOPs can provide insights into the prediction of differences in respiratory sensitivity from non-cutaneous sensitivity, an unclear regulatory requirement \[[@CR25]\]. The AOP not only provides a mechanistic understanding of how the processes of skin and respiratory sensitization differ from each other, but also the need for further research to confirm the uncertainty of chemical respiratory sensitization \[[@CR26]\]. Allergic hypersensitivity to the respiratory tract by chemicals is associated with rhinitis and asthma and remains an important occupational health problem. Recently, the concept of AOP has briefly described the major steps leading to health hazards, while drawing considerable attention from the toxicologist community as a basis for developing a framework and focus on future research \[[@CR27]\]. Allergic contact dermatitis (ACD) is a hypersensitive immune response induced by small protein-reactive chemicals that can be identified and quantitatively assessed by local lymph node assays (LLNAs). Given the complexity of the ACD, a single alternative cannot replace LLNA, but integrated testing strategies (ITS) can be used to gather important information about molecular mechanisms related to skin sensitivity and to understand the molecular process of the ACD. A systematic review of in vivo studies has been carried out, and an ACD molecular map is prepared. Also, limited comparisons of toxic genomes in humans and mice have revealed similarities, although additional data are needed to identify subtle differences. For insight into the molecular mechanisms represented by various in vitro systems, comparative analysis with in vitro toxicogenomic data can be used to compare new molecular in vitro methods, in addition to mathematical predictability. In addition, new classifications by in silico, in chemico, and in vitro methods can be complemented by immobilizing AOP and ACD molecular maps, thus laying the foundation for developing test strategies that accurately reflect key events of skin sensitivity \[[@CR28]\]. Many of these case studies have shown ways to inform AOP development in chemical hazard assessment \[[@CR29]\]. AOP technology provides a means of organizing and sharing knowledge of the mechanisms of chemical toxicity, including quantitative structure--activity relationships (QSAR) based on chemical and computational, in vitro, and integrated testing strategies, including toxicologically relevant readings. It comprises an explanatory method or integrated approaches to testing and assessment (IATA) that can be used as the basis for predictive techniques. The recently published OECD guideline provides guidance on what information is needed to identify and document AOP in terms of relevance and suitability \[[@CR30]\]. Nanomaterials and AOPs {#Sec9} ---------------------- According to the OECD guidelines, many AOPs have been proposed for chemically induced side effects in humans and the environment, and in particular, the toxic effects of nanomaterials differ from the general mechanism, due to their inherent properties, making them difficult to compare directly. While there are many knowledge gaps in understanding nanomaterials toxicity, more and more studies are being published on toxicological properties. AOP can be used to reasonably combine mechanical knowledge related to toxicity by nanomaterials to fill data gaps and develop toxicological testing strategies, captured by AOPs selected for chemical-induced toxicity. Much of the mechanistic knowledge that has been gained can be used to provide nanomaterial toxicity prediction modeling and hazard assessments \[[@CR31]\]. Due to the small size of the manufactured nanomaterials, there may be unknown health hazards, particularly in the working environment; the dust of certain manufactured nanomaterials affects the risk of inhalation and lung function. This fact requires rapid, cost-effective, and safe assays, such as multi-parametric high-throughput screening with cultured human lung cells. The predicted value of these in vitro tests is partially associated with mechanisms that contribute to their toxicity. Numerous adverse effects on fabricated nanomaterials, such as multi-walled carbon nanotubes due to changes in the dielectric, have been identified, one of which has recently been evaluated as carcinogenic. It is currently being used as a state-of-the-art strategy for analyzing genome effects from exposure to manufactured nanomaterials, focusing on lung disease \[[@CR32]\]. Although a variety of engineered nanomaterials are used commercially with a variety of physicochemical properties with respect to in vivo toxicity effects, an integrated framework for human health risk assessment (HHRA) of ENMs is still not established. Two-year carcinogenicity studies, clinical chemistry, and histopathological endpoints in rodents have been considered the "gold standard" for detecting substance-induced toxicity in animal models, but genome-wide expression analysis and in vivo high-throughput testing (HTS) are increasing. In addition, these assays have shown that transcriptomics can be used as an effective mechanism-based method of determining acceptable levels of exposure to nanomaterials in product development, when epidemiological studies are not possible. Chemical carcinogenicity prediction and AOPs {#Sec10} -------------------------------------------- Because some chemicals have multiple pathways of toxicity \[[@CR33]\], a chemical risk assessment must include qualitative and quantitative information for each chemical involved \[[@CR34]\]. Many international organizations have disseminated extensive information on chemical characterization, structure, toxicity, and risk assessment databases (e.g., PubChem, TOXNET and INCHEM). The US EPA generally defines and conducts a risk assessment of chemicals in four processes: risk identification, dose--response, exposure assessment, and risk analysis \[[@CR35]\]. Key components of risk assessment include MoA analysis and WoE using in vivo and in vitro experiments, absorption, distribution, metabolism, and excretion (ADME) information, generated by quantitative structure--activity relationships (QSAR) and based on statistical models, such as physiology-based toxic kinetics modeling \[[@CR36], [@CR37]\]. With the exception of low-probability but acute industrial chemical accidents, the focus is on the chronic exposure to chemicals in everyday life, and humans may be exposed to chemicals through inhalation, ingestion, and skin contact \[[@CR38]\]. For example, chronic exposure to air pollutants, such as workplace exposures, contaminated water, pesticide-exposed crops, pharmaceuticals, cosmetics, and other sources of exposure, can lead to chronic toxicity, which could be delayed or extended \[[@CR39]\]. Long-term accumulation of side effects may lead to genotoxic or nongenetic damage by increasing genetic instability, which increases the likelihood of cancer becoming an end point \[[@CR40]--[@CR43]\]. Carcinogens can cause various cellular abnormalities, due to genetic or epigenetic changes \[[@CR42]\]. AOP has a practical and robust weighting based on molecular, pathological, regulatory, and clinical knowledge, which facilitates the interpretation and integration of epidemiological studies in the hazard assessment process by describing biologically possible causes. The proposed AOP will present potential integration techniques for testing and evaluation to address the risks posed by chemicals in the future and will enable the development of biological instruments (e.g., Omics technology, stem cell culture, as well as experimental techniques, artificial tissues, etc.), using new techniques for understanding disease and toxicity that have traditionally been performed \[[@CR44]\]. The goal of this new tool is to improve chemical risk assessment and reduce uncertainty. Recently, this concept has formalized the AOP for human health and ecological risk assessment and has been adopted as an OECD test guide. Development of knowledge-based AOP {#Sec11} ---------------------------------- The implementation of AOP generates data and knowledge describing MIEs, intermediate effects, and toxic expressions (i.e., adverse outcomes), and AOP-related data can be viewed to facilitate the collection and retrieval of this information. Many research institutes have led and participated in creating flexible and standardized methods. Chemical specificity for intermediate effects is used in hazard assessment in all kinds of situations, since the OECD has adopted and developed a standard data format of OECD harmonized templates (OHT). Collecting historical data, the interim effects reported using OHT 201 were linked to each other to create an AOP, in accordance with the AOP technology framework \[[@CR30], [@CR45], [@CR46]\]. Adverse outcome pathways describe generalizations and predictable biological motivations when certain biological pathways or processes are disturbed \[[@CR13]\]. AOP represents existing knowledge linking two junctions, MIE and adverse outcome. For humidifier disinfectants, MIE is known to include ROS production, T cell reduction, and pro-inflammatory cytokine release from macrophages along the AOP. Possible AO may be causally related to major events (KE), interstitial fibrosis and pneumonia, asthma, allergic rhinitis or dermatitis, cerebrovascular and cardiovascular disease, diabetes, fetal death, premature bleeding, such as autoimmune diseases, liver and kidney toxicity, and cancer. Epidemiological and toxicological studies using national health insurance data and AOP knowledge-based big data can verify the actual risk of AO. These new methods can be used to identify potential diseases when exposed to humidifier disinfectants. Therefore, next-generation tools, such as AOP and pathway-based toxicology, can be an appropriate way to clarify the toxicological effects of humidifier disinfectants. Previous reports have estimated that about two million people will be affected by a humidifier disinfectant, whether cured or not, and previous studies have shown specific findings focused on epilepsy fibrosis, compared to other diseases. AOP has been recommended as a new approach to understanding the overall impact of humidifier disinfectants, and epidemiological and toxicological studies using national health insurance data and AOP knowledge-based big data can identify the actual risk of toxic expression and apply this new method. This will provide a list of potential diseases when exposed to humidifier disinfectants \[[@CR47]\]. In MIEs from humidifier disinfectants, according to a study by Song et al. \[[@CR48]\], the administration of polyhexamethylene guanidine (PHMG) in the thymus causes elevation of pre-inflammatory cytokines and lung infiltration of immune cells. Reducing the total cell count and the ratio of CD4^+^/CD8^+^ cells, histopathological examination showed a significant decrease in the cortex and medulla, and mRNA levels with T cell development were also significantly reduced. It was suggested that lung tissue exposure to PHMG not only causes lung inflammation and fibrosis, but also decreases cellular immunity \[[@CR49], [@CR50]\]. Discussion {#Sec12} ========== Application of AOP in occupational health {#Sec13} ----------------------------------------- AOP's conceptual framework, based on exposure and hazard data interpreted using risk assessment tools for product and environmental safety, can be used to understand side effects as a series of events or processes within biological systems and to improve current hazard assessment. While the precise definition of the MIE of a compound has not yet reached general acceptance, MIE is the initial interaction between a molecule and a biomolecule or biological system that may be causally related to the outcome through a route, the case study, and the issue of definition being addressed. Thus, the field can explore ways to use multiple processes of chemical knowledge to help further definition, classification, characterization, and hazard assessment and suggests the role of MIE research in the development of in vitro and in silico toxicology; studies are underway to identify and characterize MIE by a combination of chemical approaches \[[@CR51]\]. The future application of AOP is in the possibility of predicting a decrease in lung function in humans exposed to potentially harmful inhalation toxicants; and in this context, the proposed AOP screens compounds that may pose a risk to humans during inhalation exposure. Cost-effective in vitro assays that can be further classified according to the degree of toxicity that may occur are being developed \[[@CR52]\]. At the same time, biomarkers for developing preclinical endpoints that indicate the risk of death associated with a future disease or impaired lung function can also be derived from AOP \[[@CR53]--[@CR56]\]. In many studies, it is important to determine whether subsequent events, such as increased ROS levels compared to fresh air, include AOP-based EGFR activation and downstream signaling. AOP is a key combination of appropriate in vitro models and tests. It can provide a framework for the systematic assessment of events (KE). In addition, such AOP-based in vitro testing may ultimately be useful in knowing the dangers of chemicals and reducing their use \[[@CR11], [@CR57]--[@CR61]\]. Adverse outcome pathways can play a role in integrating knowledge derived from a variety of sources, including experimental data, as well as evolution-based models. This will enable more efficient application of AOP knowledge of future extrapolation of species, as well as quantitative chemistry and site-specific hazard assessments \[[@CR62]\]. Newly proposed AOPs can serve a variety of purposes, including the establishment of structure--activity relationships (SARs), the development of new in vitro toxicity studies, and the refinement of priority strategies \[[@CR12]\]. While genetic and epigenetic data usage for the prediction and identification of chemical hazards is growing, further research is needed to confirm MoA and AOP at a limited level, before the risk of dose--response modeling, exposure and/or risk assessment, and genetic/epigenetic variation is quantified. Evaluating gene--environment interactions is the basis from which genetic and epigenetic (epigenomic) data can be used for hazard and risk assessment. In vivo and in vitro data should be supplemented with human data collected from occupational health and molecular epidemiological studies. Research needs to be designed to provide as much information as possible about the relationship between genetic and epigenetic mutations and toxic pathways. In addition, attention should be paid to ethical, legal, social, and political impacts when genetic and epigenetic (epigenomic) data are used for occupational health issues. Ultimately, studies published before genetic and epigenetic data are used to assess occupational health, and the development of occupational exposure levels (OELs) should demonstrate that these changes affect occupational exposure and toxic expression \[[@CR63]\]; the use of computational biology and toxicogenic pathways will increasingly focus on consistent physiological changes between similar groups of toxic substances \[[@CR64], [@CR65]\]. Developing non-animal testing techniques that utilize route-based machine information can provide more predictive tools for identifying potential risks, as well as more information on LC~50~ or other in vivo observations. Extrapolating animal data to predict health effects may include physiological, anatomical, and metabolic differences between species (e.g., other airway dichotomy, cell type and composition, other biomodified enzymes and respiratory patterns, metabolic rate, physiological changes) \[[@CR66]\]. It should also be sufficient to predict and manage potential adverse outcomes in humans \[[@CR67]--[@CR70]\]. Application for inhalation toxicity {#Sec14} ----------------------------------- The discovery of various AOPs after inhalation exposure opens the door to the development of in vitro and in silico technologies to assess AOP-related endpoints that can explain toxic expression at the organism and/or population level \[[@CR13], [@CR14]\]. These AOP tools provide more reliable information, assess target organ impacts, and help better understand how certain toxic chemicals affect humans (i.e., providing mechanical insight values beyond what can be collected in the LC~50~). This technology has become a promising field of research that has not yet been accepted by international regulatory bodies \[[@CR71]\], and this review discusses the development of integrated approaches to testing and assessment (IATA) that can replace the use of animals to assess the inhalation toxicity of chemicals. As more data and tools become available and understanding of the toxic mechanisms progresses, optimal technologies will continue to evolve. In addition to acute inhalation toxicity, many cellular systems and concepts can be applied to long-term repeated inhalation studies \[[@CR72]\]. New approaches are needed to assess the outcomes of inhalation toxicants on workers' health, and these techniques will be based on the toxic mechanisms, understanding of dose measurement, in silico modeling, and in vitro testing. To accelerate the widespread implementation of these techniques, the development of AOP can help resolve data gaps by understanding models and mechanisms and can be used to investigate and optimize key events. Advances in the twenty-first-century life sciences are important to provide an unprecedented opportunity to gain a dynamic understanding of the causes and pathophysiology of disease and a concrete understanding of human beings, and to consider the ongoing trial and error of research, drug development, and clinical use \[[@CR73]\]. Although new technologies can also be applied to environmental health and disease, these advances require new medical and drug development paradigms for maximum benefit. Human diseases should be used in systems toxicology for integrating and interpreting data on the cause of disease and pathophysiology, with studies focused on human-specific models for understanding AOPs at different biological levels, similar to those of toxicology \[[@CR74], [@CR75]\]. It is now time for an integrated discourse to identify and consider the many challenges and questions that need to be addressed. This review summarizes current scientific advances on the mechanisms and assays that can be used to assess the inhalation toxicity of chemicals from the perspective of protecting workers' health. Although there are few QSAR models currently available for predicting inhalation toxicity, the applicability areas of QSAR (e.g., TopKAT and MultiCASE) are examined to determine whether a model can be optimized for occupational toxicity prediction. It is necessary to identify the differences between the advantages of existing models and to clarify which models can be used for specific applications. Also, new models can be developed using data collected from other sources, and the US EPA Center for computational toxicology (<https://comptox.epa.gov/dashboard/>) is a convenient platform to accommodate available models and their predictions \[[@CR71]\]. It is important to carefully assess the variability associated with in vivo data that rely on developing new models to quantify the uncertainty associated with model prediction, and best practice protocols are being developed in in silico methods involving various endpoints \[[@CR76]\]. There are also a number of AOPs involved in exposure, but additional AOPs need to develop specific toxic expressions that may occur with inhalation exposure. This will be useful for the ongoing construction of AOP on mechanisms of inhalation toxicity. AOP development can be used for the likelihood of causing specific toxicity and to establish confidence in in vitro tests characterizing key events (KEs). For example, each researcher should also be encouraged to work with an AOP expert to bridge the gap between AOP development and knowledge, by providing an interactive virtual platform for AOP using an AOP-Wiki designed to create international consensus on the developed AOP. Many systems can be used for the evaluation of inhalable toxicants, but cell-based systems also need to be specific for their ability to metabolize compounds. In particular, three-dimensional (3D) tissue and lung-on-a-chip models are believed to represent human characteristics, but should be developed as a standardized test protocol to maintain consistency between laboratories. Designing comprehensive assays for inhalation toxicity requires the use of AOPs, alternative or non-test methods, and in vitro assays. Experts with a variety of expertise (in vitro, in vivo inhalation toxicity, computational modeling, exposure science, etc.) should work together to design this approach. A key step in this process is proof-of-concept testing that focuses on specific chemicals, such as industrial and environmental toxicants, pesticides, tobacco, or pharmaceuticals, and is useful in describing key events in the pathogenesis for a particular AOP. The development and implementation of non-animal assays for inhalation toxicity testing and the acceptance of global regulations require cooperation between various stakeholders, and the International Science Consortium and the NTP Interagency Center for the Evaluation of Alternative Toxicological Methods (NICEATM) have formed a working group. Researchers' participation is encouraged in these activities. The success in this area will develop platforms that can predict mortality and preventive effects from inhalation exposure, and these new techniques will lead to a better understanding of toxic mechanisms, without the use of animals, unleashing the potential of protecting workers' health for science of the twenty-first century. Methods {#Sec2} ======= This study examined the concept of AOP on workers' chemical exposure and prospects in occupational health. This review provides a summary of the current literature on AOP in occupational health, risk assessment of respiratory and nanomaterials, and prediction of carcinogenicity. Major Web sites were searched, specifically Google Scholar (<http://scholar.google.com>), ScienceDirect ([www.sciencedirect.com](http://www.sciencedirect.com)), Scopus ([www.scopus.com](http://www.scopus.com)), NDSL (<http://www.ndsl.kr/index.do>), and PubMed (<http://www.ncbi.nlm.nih.gov/pubmed>). The following key terms were used: "Adverse outcome pathway," "Toxicology," "Risk assessment," "Human exposure," "Worker," and "Occupational safety and health." Among the literature searched through this process, the literature on toxic expression pathways (AOPs) was intended to utilize the most recent reports (after 2015), and the data on the research process and basic concepts that are presented for ease of explanation are not only from 2015, but also include some data from before 2015. To accomplish the objective of this review, two categories of papers were selected: "AOP concept" and "Trends and applications of AOPs in occupational health." Approximately 100 papers appeared in search engine results, with 75 papers meeting inclusion criteria for detailed analysis. Information from these 75 papers regarding measures for worker safety in the prospects for AOP in industry and occupational health has been summarized in this paper. Conclusion {#Sec15} ========== In order to fully understand adverse outcome pathway (AOP), it is necessary to consider the nature of genetic and epigenetic information. The assessment of the hazard and risk of industrial chemicals requires the results of in vitro, in vivo, and epidemiological studies on genetic and epigenetic factors and quantitative risk assessment studies. However, despite the great potential, little genetic or epigenetic (epigenomic) information has been used in the quantitative risk assessment of occupational and/or environmental exposures, and the number of studies containing this information will increase in the future. Adverse outcome pathway is a conceptual tool that delineates the causal pathways of chemical toxicity. The goal of AOP is to accurately predict the toxicity of chemicals, by serving as an alternative to traditional chemical risk assessment. First introduced for ecological toxicity, AOP is now widely used in chemical assessments. The AOP, which is applied to inhalation toxicity especially carcinogenicity assessment, will be a tool to understand the effects of the use of chemicals in the workplace and the chronic exposure of the workers involved and make their predictions very useful. Based on this forecasting tool, it is expected to bring dramatic advances in occupational and environmental cancer prevention. This study was supported by the Korean Occupational Safety and Health Agency (Ulsan, Republic of Korea), the Ministry of Employment and Labor (Sejong, Republic of Korea), and a Grant-in-Aid for chemicals hazard evaluation (2019). Funding was provided by OSHRI, KOSHA. Kyung-Taek Rim declares that he has no conflict of interest. This article does not contain any studies with human participants or animals performed by any of the authors.
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What Is Sclerotherapy? Sclerotherapy is a procedure used to treat blood vessels or blood vessel malformations (vascular malformations) and also those of the lymphatic system. A medicine is injected into the vessels, which makes them shrink. It is used for children and young adults with vascular or lymphatic malformations. In adults, sclerotherapy is often used to treat varicose veins and hemorrhoids. Sclerotherapy has been used in the treatment of varicose veins for over 150 years. Like varicose vein surgery, sclerotherapy techniques have evolved during that time. Modern techniques including ultrasonographic guidance and foam sclerotherapy are the latest developments in this evolution. The first reported attempt at sclerotherapy was by D Zollikofer in Switzerland, 1682 who injected an acid into a vein to induce thrombus formation. Both Debout and Cassaignaic reported success in treating varicose veins by injecting perchlorate of iron in 1853. Desgranges in 1854 cured 16 cases of varicose veins by injecting iodine and tannin into the veins. This was approximately 12 years after the probable advent of great saphenous vein stripping in 1844 by Madelung. However, due to high rates of side-effects with the drugs used at the time, sclerotherapy had been practically abandoned by 1894. With the improvements in surgical techniques and anesthetics over that time, stripping became the treatment of choice. George Fegan in the 1960s reported treating over 13,000 patients with sclerotherapy, significantly advancing the technique by focussing on fibrosis of the vein rather than thrombosis, concentrating on controlling significant points of reflux, and emphasizing the importance of compression of the treated leg. The procedure became medically accepted in mainland Europe during that time. However it was poorly understood or accepted in England or the United States, a situation that continues to this day amongst some sections of the medical community. The next major development in the evolution of sclerotherapy was the advent of duplex ultrasonography in the 1980s and its incorporation into the practice of sclerotherapy later that decade. Knight was an early advocate of this new procedure and presented it at several conferences in Europe and the United States. The work of Cabrera and Monfreaux in utilizing foam sclerotherapy along with Tessari's "3-way tap method" of foam production further revolutionized the treatment of larger varicose veins with sclerotherapy.
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Psoriasis :: What Is Psoriasis? Psoriasis is a skin disease that causes scaling and swelling. Skin cells grow deep in the skin and slowly rise to the surface. This process is called cell turnover, and it takes about a month. With psoriasis, it can happen in just a few days because the cells rise too fast and pile up on the surface. Most psoriasis causes patches of thick, red skin with silvery scales. These patches can itch or feel sore. They are often found on the elbows, knees, other parts of the legs, scalp, lower back, face, palms, and soles of the feet. But they can show up other places such as fingernails, toenails, genitals, and inside the mouth. Who Gets Psoriasis? Anyone can get psoriasis, but it occurs more often in adults. Sometimes there is a family history of psoriasis. Certain genes have been linked to the disease. Men and women get psoriasis at about the same rate. What Causes Psoriasis? Psoriasis begins in the immune system, mainly with a type of white blood cell called a T cell. T cells help protect the body against infection and disease. With psoriasis, T cells are put into action by mistake. They become so active that they set off other immune responses. This leads to swelling and fast turnover of skin cells. People with psoriasis may notice that sometimes the skin gets better and sometimes it gets worse. Things that can cause the skin to get worse include: Infections Stress Changes in weather that dry the skin Certain medicines. How Is Psoriasis Diagnosed? Psoriasis can be hard to diagnose because it can look like other skin diseases. The doctor might need to look at a small skin sample under a microscope. How Is Psoriasis Treated? Treatment depends on: How serious the disease is The size of the psoriasis patches The type of psoriasis How the patient reacts to certain treatments. All treatments don’t work the same for everyone. Doctors may switch treatments if one doesn’t work, if there is a bad reaction, or if the treatment stops working. Topical Treatment: Treatments applied right on the skin (creams, ointments) may help. Treatments can: Help reduce swelling and skin cell turnover Suppress the immune system Help the skin peel and unclog pores Reduce cell turnover and swelling. Bath solutions and lotions may feel good, but they rarely make the skin better. They are often used along with stronger treatments. Light Therapy: Natural ultraviolet light from the sun and artificial ultraviolet light are used to treat psoriasis. One treatment, called PUVA, uses a combination of a drug that makes skin more sensitive to light and ultraviolet A light. Systemic Treatment: If the psoriasis is severe, doctors might prescribe drugs or give medicine through a shot. This is called systemic treatment. Antibiotics are not used to treat psoriasis unless bacteria make the psoriasis worse. Combination Therapy: When you combine topical (put on the skin), light, and systemic treatments, you can often use lower doses of each. Combination therapy can also lead to better results. What Are Some Promising Areas of Psoriasis Research? Doctors are learning more about psoriasis by studying: Genes New treatments that help skin not react to the immune system Laser light treatment on thick patches.
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