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Dust Collisions Could Transport Microbial Life to Other Planets Written By In Brief Microbial life lofted into Earth’s upper atmosphere could be sputtering into space thanks to collisions with interplanetary dust streams, potentially resulting in life being transported from planet to planet. The Solar System is filled with dust, left over from the formation of the planets, produced by asteroid collisions and expelled by comets. Professor Arjun Berera, a […] Microbial life lofted into Earth’s upper atmosphere could be sputtering into space thanks to collisions with interplanetary dust streams, potentially resulting in life being transported from planet to planet. The Solar System is filled with dust, left over from the formation of the planets, produced by asteroid collisions and expelled by comets. Professor Arjun Berera, a physicist at the University of Edinburgh, UK, has modeled how streams of interplanetary dust impact Earth’s atmosphere at velocities of up to 70 kilometers (43.5 miles) per second. Writing in the journal Astrobiology, Berera finds that the dust impacts provide enough energy to knock atmospheric molecules, as well as any organic matter or microbes that may exist at altitudes of 150 kilometers (93 miles), free of Earth’s gravity and into space. The findings provide a potential mode of transport for organic matter between planets, raising the possibility that life could have begun elsewhere in the Solar System before being transported to Earth, or vis versa. However, Berera admits that there are caveats to his work. Number one is that no life has ever been found 150 kilometers above Earth’s surface. However, there are ways to feasibly transport microbes up there, such as vertical winds in the upper atmosphere, and phenomena linked to thunderstorms such as sprites and blue jets. “What my calculations show is that one would need just a vanishingly small concentration [of life] at 150 kilometers altitude for my mechanism to work,” Berera tells Astrobiology Magazine. Have microbes ejected from Earth’s atmosphere made their way to Mars? Have microbes ejected from Mars ever made their way to Earth? Image Credit: NASA/JPL–Caltech. Another potential problem is the high-velocity impacts of dust particles striking microbes could kill them. Previous studies, says Berera, have shown that bacteria can survive shock pressures of 50 gigapascal, and Berera’s calculations indicate that in some cases the dust collisions will inflict shock pressures less than that. However, he sees this as a major factor in limiting how many microbes can escape into space. Although Berera’s work shows how microbes could escape Earth, his research indicates that “it is extremely difficult for any small organisms to escape Earth’s gravity, since many things have to come together,” he says. “More research is now needed to assess what the concentration of biological material is high up in the atmosphere, how well it could withstand the violent blows of collisions with space dust and how well it could survive in space.” The research was funded by the UK’s Science and Technology Facilities Council.
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INTRODUCTION {#h0.0} ============ *Klebsiella pneumoniae* is a pathogenic Gram-negative bacterium that is a member of the *Enterobacteriaceae* family. While the bacterium is normally found in the flora of human skin, mouth, and intestinal tract, it is also well characterized as an opportunistic pathogen ([@B1], [@B2]). *K. pneumoniae* infections are associated with hospitalized patients with a weakened immune system. The bacterium causes a wide range of human diseases that include urinary tract infections, pyogenic liver abscess (PLA), and pneumonia ([@B1], [@B3]). Due to the alarming increase in carbapenem-resistant *Enterobacteriaceae* (CRE), of which *K. pneumoniae* comprises the majority of infections, the Centers for Disease Control (CDC) have designated these bacteria as an urgent threat to public health ([@B4]). Because of the decreasing efficacy of antibiotics against *K. pneumoniae*, new treatment modalities must be developed, and a promising approach is through identifying bacterial factors required to cause disease. The few virulence factors identified to date include capsule and lipopolysaccharide (LPS), which vary by structure and serotype, and adhesins and siderophores, which vary in frequency among clinical isolates ([@B1], [@B5][@B6][@B7]). To develop novel therapies that will be broadly effective against *K. pneumoniae*, conserved targets must be identified. Barriers to identifying new *K. pneumoniae* virulence factors include limitations with genetic sequencing techniques and the difficulties in manipulating the *K. pneumoniae* chromosome. In recent years, newer approaches such as transposon insertion site sequencing (InSeq) have allowed for greatly enhanced genetic screening. This method uses high-throughput sequencing to determine the frequency and chromosomal location of thousands of transposon mutations from a large pool of mutants in a single experiment ([@B8], [@B9]). InSeq requires a fully sequenced genome and confirmation of mutant phenotypes by either simultaneously constructing an indexed transposon mutant library or constructing mutants in selected genes that elicit fitness defects. Because of advances in genetic sequencing, a number of high-quality reference sequences of *K. pneumoniae* are now available ([@B10][@B11][@B13]). However, many of the standard methods for gene replacement in *Escherichia coli*, such as suicide vector conjugation and linear DNA homologous recombination, are less efficient in *K. pneumoniae* or are complicated by intrinsic and acquired antibiotic resistance ([@B14]). The Lambda Red recombinase system, which is incredibly efficient in *E. coli* ([@B15]), could greatly increase the efficiency of gene recombination in *K. pneumoniae* ([@B16]). These advances now provide the ability to rigorously screen the genome for novel genes that contribute to virulence or *in vivo* fitness. Using this new sequencing approach and the Lambda Red recombinase system, we have identified numerous novel *K. pneumoniae* fitness genes required to infect the lung in a mouse model of pneumonia. RESULTS {#h1} ======= Transposon library construction, inoculation, and validation. {#s1.1} ------------------------------------------------------------- *K. pneumoniae* KPPR1 causes acute pneumonia complicated by bacteremia in a well-established murine model ([@B5], [@B6]). To facilitate InSeq analysis, the KPPR1 genome was sequenced to generate a single, gapless contig and the genes contained in it were annotated ([@B10]). The genome contains 5,191 predicted genes, including 25 rRNA, 85 tRNA, and 5,081 protein-coding sequences. To identify fitness factors required during lung infection, a library of \~25,000 transposon mutants was constructed to provide 99% genome coverage. Colony PCR and Southern blotting of representative transconjugants indicated that the library contained single, random transposon insertions at varied locations in the chromosome without integration of the vector (see [Fig. S1](#figS1){ref-type="supplementary-material"} in the supplemental material). This library was inoculated into mice using an aspiration model of pneumonia at a dose of 1.4 × 10^6^ CFU ([@B5], [@B10], [@B17]). After 24 h, the mean bacterial density increased to 5 × 10^6^ CFU in the lung ([Fig. 1A](#fig1){ref-type="fig"}). To quantify and map each transposon onto the chromosome, genomic DNA was extracted from the inoculum and lung homogenates, and transposon junction fragments were generated. These fragments were sequenced using an Illumina HiSeq2500 instrument, mapped to the chromosome, and enumerated based on read count ([@B18]). Each sample had at least 68 million reads corresponding to 25,346 unique transposon insertions within genes (see [Table S1](#tabS1){ref-type="supplementary-material"}), meeting the coverage goal as stated above. Of 5,191 predicted genes, 4,312 had at least one insertion detected, whereas 879 genes did not. Because the transconjugants were required to grow to a colony for inclusion in the library, genes without insertions may be essential. However, a larger mutagenesis library would be required to estimate more precisely the number of essential genes ([@B8]). ![InSeq analysis indicates that fitness genes are important during pneumonia based on differential transposon read counts between the inoculum and mouse lung. Mice (*n* = 5) inoculated with 1.4 × 10^6^ CFU of a pool of \~25,000 transposon mutants for 24 h were sacrificed and cultured on LB agar for CFU (A) or for DNA extraction, Illumina sequencing of transposon junctions, and read alignment with the KPPR1 genome to map and count transposon insertions. The locations and frequencies of transposon insertions in *ilvD* (B) and *VK055_468* (C) are shown.](mbo0031523580001){#fig1} InSeq analysis identifies hundreds of potential *K. pneumoniae* lung fitness factors. {#s1.2} ------------------------------------------------------------------------------------- To identify *in vivo* fitness genes, the numbers of transposon insertion reads within each gene were compared between the lung and inoculum pools. Of genes with insertions, 3,880 had at least one shared transposon between the inoculum and lung samples (see [Data Set S1](#dataS1){ref-type="supplementary-material"} in the supplemental material) and were used for subsequent analysis. Since input and output data are "paired" in nature for each insertion, a *P* value was calculated for each insertion using an exact Poisson test and then combined into a single *P* value for each gene using Fisher's method. This method is similar to an approach called CEDER, which uses information from each exon of a eukaryotic gene to determine if there is consistent differential expression in RNA transcriptome sequencing (RNA-Seq) data for a given gene ([@B19]). Therefore, we call this *P* value a CEDER *P* value. Genes were sorted based on their fitness factor (total insertion counts in the inoculum/total insertion counts in the lung) and their CEDER *P* value (see [Data Set S3](#dataS3){ref-type="supplementary-material"}). Inspection of transposon numbers and counts in individual genes suggested that the CEDER *P* value could be used as a selection criterion for true-positive results of identification of fitness genes by InSeq. For example, *ilvD*, required for branched-chain amino acid (BCAA) synthesis, had a *P* value of 0 based on 18 insertions in the input and 13 in the lung with 11 shared insertions having an average fitness factor of 192 ([Fig. 1B](#fig1){ref-type="fig"}). In contrast, *VK055_468*, a putative transcriptional regulatory gene, had a CEDER *P* value of 2e−14 based on a 186-fold fitness factor but only one insertion ([Fig. 1C](#fig1){ref-type="fig"}). To confirm fitness defects and test the predictive power of CEDER, seven potential fitness genes identified by InSeq analysis were selected for experimental validation by coinfection. Six genes (*rfaH*, *ilvC*, *ilvD*, *copA*, *aroE*, and *VK055_4417*) with a CEDER *P* value of 0 and a fitness factor of \>10 were tested compared to *VK055_468* (*P* = 2e−14; fitness factor of 168). These genes were mutated using Lambda Red recombinase to replace the entire coding sequence with a kanamycin resistance gene ([@B15]). Mice were then infected as described in Materials and Methods, but with a 1:1 ratio of the wild type (WT) and each mutant. Based on the bacterial density of each strain after 24 h, the competitive index was calculated. All six mutants with a CEDER *P* value of 0 had a fitness defect in the lung compared to the wild type ([Fig. 2](#fig2){ref-type="fig"}), ranging from 1.4-fold (*VK055_4417*) to 11,694-fold (*rfaH*). In contrast, *VK055_468* did not have a fitness defect compared to the wild type ([Fig. 2](#fig2){ref-type="fig"}). Therefore, genes with a CEDER *P* value of \>0 were not characterized further. In total, 1272 genes had a *P* value of 0 (top 25 shown in [Table 1](#tab1){ref-type="table"}), including 69 genes with a fitness factor of \>10 and 333 genes with a fitness factor of \>2. There were also 452 genes with a fitness factor of \<0.5 and 97 genes with a fitness factor of \<0.1, suggesting that insertion mutants increase lung fitness. Since the goal of the study was to identify mutants with decreased lung fitness, mutants overrepresented in the lung were not pursued further. ![Competitive infection against the wild-type strain confirms the fitness defect of mutants selected by InSeq. Insertion-deletion mutants of six genes selected and one gene not selected by CEDER analysis (*VK055_468*) of InSeq fitness were constructed using Lambda Red recombinase and used to coinfect mouse lungs with the wild type (WT), or WT carrying pACYC184 where noted, at a 1:1 ratio in a total inoculum of 1 × 10^6^ CFU. Mean competitive index (log~10~) for each mutant compared to the wild type at 24 h is shown. \*, *P* \< 0.05; \*\*, *P* \< 0.01; \*\*\*, *P* \< 0.001, by one-sample *t* test on log~10~-transformed data (≥4 mice per group); \#\#\#, *P* \< 0.001 by two-sample *t* test.](mbo0031523580002){#fig2} ###### Top 25 *K. pneumoniae* KPPR1 lung fitness genes[^a^](#ngtab1.1){ref-type="table-fn"} Locus ID (*VK055*\_*x*) Gene Product Ratio (input/lung) ------------------------- ------------ --------------------------------------------------------------- -------------------- *5014* Capsule assembly Wzi family protein 2820.95 ***3141*** ***rfaH*** **Transcriptional activator** **2696.77** *5096* Hypothetical protein 2486.08 ***3202*** ***ilvC*** **Ketol-acid reductoisomerase** **2248.61** *3832* *argR* Arginine repressor 1140.74 *5025* Undecaprenyl-phosphate glucose phosphotransferase 840.55 *5012* *galF* Regulatory protein 704.99 *3206* *ilvE* Branched-chain amino acid aminotransferase 581.10 *3515* Rhodanese-like domain protein 508.09 ***4417*** **MarR family protein** **442.14** *4811* *purF* Amidophosphoribosyltransferase 378.16 *4619* *purL* Phosphoribosylformylglycinamidine synthase 312.03 *1194* *trpD* Anthranilate synthase component II 301.31 *4135* *serA* [d]{.smallcaps}-3-Phosphoglycerate dehydrogenase; provisional 248.61 *2495* *leuC* 3-Isopropylmalate isomerase subunit, dehydratase component 246.77 *3142* *tatC* Twin arginine-targeting protein translocase 219.96 ***3205*** ***ilvD*** **Dihydroxy acid dehydratase** **203.61** *5023* Hypothetical protein 172.11 *4883* *rcsB* Transcriptional regulator 126.39 *2215* *phoR* Phosphate regulon sensor kinase 110.92 *4579* *pheA* Bifunctional chorismate mutase/prephenate dehydratase 94.55 *3368* 2-Oxo-3-deoxygalactonate 6-phosphate aldolase 90.01 ***2084*** ***copA*** **Copper-translocating P-type ATPase** **69.70** *3086* *purH* Phosphoribosylaminoimidazole carboxamide formyltransferase 66.84 ***3791*** ***aroE*** **Dehydroshikimate reductase** **61.93** Experimentally validated genes are shown in boldface. *rfaH* is required for serum resistance. {#s1.3} ---------------------------------------- RfaH is an antiterminator that specifically promotes the transcription of long virulence operons, including capsule and lipopolysaccharide (LPS) synthesis genes, in *E. coli* and *Salmonella enterica* serotype Typhimurium ([@B20][@B21][@B22]). In KPPR1, an *rfaH* mutant is severely attenuated in the lung (\>10,000-fold compared to wild type), and the fitness of the mutant is significantly restored by complementation with the *rfaH* gene ligated into pACYC184 ([Fig. 2](#fig2){ref-type="fig"}). This mutant forms a small colony compared to the wild type, suggesting a defect in capsule biosynthesis. Indeed, India ink staining of bacteria delineated copious capsule in KPPR1 but no visible capsule in the *rfaH* mutant ([Fig. 3A and B](#fig3){ref-type="fig"}). To assess mucoviscosity, a phenotype associated with hypervirulent capsular serotypes in *K. pneumoniae* clinical isolates, low-speed centrifugation was performed and the optical density of the supernatant was measured ([@B23], [@B24]). Whereas the wild-type suspension remained turbid, the *rfaH* mutant pelleted readily, and complementation restored mucoviscosity significantly ([Fig. 3D](#fig3){ref-type="fig"}). Both capsule and O antigen of LPS can contribute to resistance to complement-mediated killing ([@B25]), which has been correlated with the ability to cause patient infections ([@B1]). Incubation of the *rfaH* mutant in serum demonstrated a \>1,000-fold loss in viability, greater than that for the susceptible control strain KP297, whereas there was no loss of viability in the wild type ([Fig. 4](#fig4){ref-type="fig"}). Complementation restored serum resistance. In RPMI medium with 10% heat-inactivated serum, complement is disabled and *K. pneumoniae* grows robustly but requires the siderophore enterobactin or its glycosylated derivative salmochelin to acquire iron; yersiniabactin does not support growth under this condition ([@B5], [@B26]). Whereas the wild type replicates robustly, the *rfaH* mutant had a moderate growth defect comparable to the loss of salmochelin expression (*iroA ybtS* mutant) but not as severe as the siderophore null *entB ybtS* mutant ([Fig. 5](#fig5){ref-type="fig"}). In contrast, the *rfaH* mutant grew well in RPMI medium without added serum (see [Fig. S2A](#figS2){ref-type="supplementary-material"} in the supplemental material). Together, these data indicate that *rfaH* is required for wild-type capsule production, to resist complement-mediated serum killing, and for maximal growth in iron-limited serum. ![The *rfaH* mutant is deficient in extracellular capsule. (A to C) India ink staining of *K. pneumoniae* KPPR1 (WT) (A) and isogenic *rfaH* (B) and *aroE* (C) mutants after overnight culture in LB broth is shown by phase-contrast microscopy, in which the presence of capsule is indicated by an area of negative staining around the bacteria. Magnification, ×1,000. (D) Mucoviscosity, as measured by optical density (OD~600~) after centrifugation for 5 min at 1,000 × *g* with a starting turbidity of 1.0, is shown as the mean and standard deviation from 6 biological replicates. \*, *P* \< 0.0001 by ANOVA with Fisher's LSD test compared to the wild type; \#, *P* \< 0.0001 compared to both WT carrying pACYC and the *rfaH* mutant carrying pRfaH.](mbo0031523580003){#fig3} ![The *K. pneumoniae* rfaH and *aroE* mutants are susceptible to serum killing. Viability of *K. pneumoniae* KPPR1 (WT) and isogenic mutants, without (A) or containing pACYC184 with or without *rfaH* (B), after a 3-h incubation in human serum is shown as mean log~10~ CFU/ml ± standard deviation from at least two replicates per group. \*, *P* \< 0.0001 by ANOVA with Fisher's LSD test compared to the wild type.](mbo0031523580004){#fig4} ![The *K. pneumoniae* *rfaH* mutant has a mild growth defect in heat-inactivated serum. *K. pneumoniae* KPPR1 (WT) and isogenic mutant growth (log~10~ CFU/ml) after overnight incubation of a 1 × 10^3^-CFU/ml inoculum in RPMI medium supplemented with 10% heat-inactivated serum is shown as the mean ± standard deviation from 4 independent experiments. \*, *P* \< 0.05; \*\*, *P* \< 0.01; \*\*\*\*, *P* \< 0.0001, by ANOVA with Fisher's LSD test.](mbo0031523580005){#fig5} *K. pneumoniae* requires branched-chain amino acid synthesis for full virulence. {#s1.4} -------------------------------------------------------------------------------- The *ilv* locus encodes enzymes for synthesis of the branched-chain amino acids isoleucine and valine and the precursors for leucine ([@B27]). *ilvC* and *ilvD* mutants had 100- and 66-fold defects in competition with the wild type ([Fig. 2](#fig2){ref-type="fig"}), respectively, indicating that branched-chain amino acid synthesis is required for fitness in the lung. To confirm that the *ilvC* and *ilvD* mutants are auxotrophs for branched-chain amino acids, their growth in minimal medium was compared to that of the wild type ([Fig. 6](#fig6){ref-type="fig"}). Neither mutant grew significantly, but growth of both was restored by supplementation of the medium with the branched-chain amino acids isoleucine and valine at 10 mM concentrations. These data indicate that synthesis of branched-chain amino acids is required for lung fitness. ![*K. pneumoniae* ilvC and *ilvD* mutants are unable to replicate in minimal medium without branched-chain amino acids. Optical density (OD~600~) of *K. pneumoniae* KPPR1 (WT) and *ilvC* and *ilvD* mutants in M9 minimal medium with or without 10 mM isoleucine (I) and valine (V) is shown as the mean from triplicate samples representative of 3 independent experiments.](mbo0031523580006){#fig6} *aroE* is required for serum resistance. {#s1.5} ---------------------------------------- Disruption of the *aroE* gene, which encodes shikimate dehydrogenase required for aromatic amino acid synthesis, causes a 13-fold decrease in fitness in competitive infection ([Fig. 2](#fig2){ref-type="fig"}). Unlike for *ilvC* and *ilvD* mutants, the *aroE* mutant is not defective for growth in minimal medium (see [Fig. S2B](#figS2){ref-type="supplementary-material"} in the supplemental material), perhaps due to compensation by the *ydiB*-encoded quinate/shikimate dehydrogenase ([@B10], [@B28]). However, the *aroE* mutant does have a moderate defect in serum survival ([Fig. 4](#fig4){ref-type="fig"}) and a defect in mucoviscosity ([Fig. 3D](#fig3){ref-type="fig"}), despite production of capsule as measured by India ink ([Fig. 3C](#fig3){ref-type="fig"}). These data indicate that *aroE* is dispensable for bacterial growth *in vitro* but is required to evade complement-mediated serum killing. *copA* is required to prevent copper toxicity. {#s1.6} ---------------------------------------------- Mutation of the *copA* gene, encoding a P-type ATPase copper efflux pump ([@B29]), causes a 37-fold fitness defect in competitive infection with the wild type ([Fig. 2](#fig2){ref-type="fig"}). To determine whether deletion of *copA* increases susceptibility to copper toxicity, as seen in *E. coli*, the wild type and *copA* mutant were incubated in M9 minimal medium with increasing amounts of copper (5 to 25 µM). We found that CFU are significantly lower in *copA* mutants on average (*P* = 0.02) and the rate of decreasing CFU with increasing Cu concentration is significantly higher in a *copA* mutant (*P* = 0.0003) than in the wild type (WT) ([Fig. 7A](#fig7){ref-type="fig"}). Complementation with a plasmid-expressed copy of *copA* restored copper resistance to the mutant ([Fig. 7B](#fig7){ref-type="fig"}). In *E. coli*, copper toxicity occurs through inactivation of dehydratases such as IlvD in the branched-chain synthesis pathway ([@B30]). The *ilvD* mutant was more resistant to copper than the *copA* mutant, suggesting additional cellular targets of copper toxicity ([Fig. 7C](#fig7){ref-type="fig"}). However, the addition of branched-chain amino acids significantly protected the *copA* mutant ([Fig. 7C](#fig7){ref-type="fig"}). These data indicate that copper resistance and branched-chain amino acid metabolism pathways may overlap in their contribution to *K. pneumoniae* lung fitness*.* ![The *K. pneumoniae* *copA* mutant has increased sensitivity to copper. (A) Viability of a 1 × 10^8^-CFU inoculum of *K. pneumoniae* WT and *copA* mutant after an 18-h incubation in M9 broth with concentrations of cupric sulfate indicated is shown as mean ± standard deviation of results from at least 3 independent experiments. Based on a linear regression model (modeling log-transformed CFU as a function of the Cu concentration, group \[WT or *copA*\], and interaction between concentration and group), the *copA* mutant has a significantly faster-decreasing rate over concentrations than the wild type (\#). (B) Viability of *K. pneumoniae* harboring pACYC184 (pACYC) or pACYC184 with *copA* (pCopA) after incubation in 25 µM CuSO~4~ is shown as the mean ± standard deviation from three independent experiments. \#, *P* \< 0.0001 compared to both strains by ANOVA with Fisher's LSD test; ns, not significant. (C) Viability of *K. pneumoniae* mutants as indicated in 25 µM CuSO~4~ with or without 10 mM isoleucine and valine is shown as the mean ± standard deviation from at least three independent experiments. \*\*\*\*, *P* \< 0.0001 by ANOVA with Fisher's LSD.](mbo0031523580007){#fig7} InSeq identifies conserved genes as critical fitness factors for *K. pneumoniae* lung infection. {#s1.7} ------------------------------------------------------------------------------------------------ To define broad pathways that may contribute to *K. pneumoniae* fitness in the lung, gene enrichment analysis was performed. The KEGG classification of the 333 genes in which mutants were \>2-fold underrepresented in the lung was determined, and the representation of each class was compared to the total gene set in the KPPR1 genome as annotated based on KEGG assignment. The pathways for 2-oxocarboxylic acid metabolism; valine, leucine, and isoleucine biosynthesis; and biosynthesis of amino acids were significantly overrepresented among genes identified as fitness factors by InSeq (corrected *P* values of \<0.01), indicating the critical importance of branched-chain amino acid synthesis during lung infection. The products of conserved fitness genes could serve as targets for novel therapeutics against *K. pneumoniae*. To identify conserved genes in other clinically significant isolates, the KPPR1 genome was compared to the following reference sequences: MGH78578, an isolate from a patient with pneumonia; NTUH-K2044, an isolate that caused a PLA; NJST258_1, a carbapenem-resistant (KPC) ST258 isolate; and Kp342, a plant endophyte. All combinations of shared, full-length chromosomal genes were analyzed, and overlapping gene sets were tabulated ([Fig. 8A](#fig8){ref-type="fig"}; see also [Data Set S3](#dataS3){ref-type="supplementary-material"} in the supplemental material). KPPR1 shares a conserved set of 3,865 genes (quadrant X; 76% of predicted protein-encoding genes) with all strains; 121 genes with human isolates MGH78578, NTUH-K2044, and NJST258_1 but not the plant endophyte Kp342 (quadrant XIV); and 20, 89, 40, and 27 genes exclusively with MGH78578 (quadrant II), NTUH-K2044 (quadrant XV), NJST258_1 (quadrant IV), and Kp342 (quadrant VIII), respectively. To assess the conservation of the top fitness genes identified by InSeq analysis, the 69 genes with a fitness factor of \>10 were mapped to the regions of overlap between KPPR1 and 4 reference genomes. In fact, 60 of 68 mapped genes were conserved between all *K. pneumoniae* isolates ([Fig. 8B](#fig8){ref-type="fig"}), and all 6 fitness genes verified by targeted mutation are conserved. These data indicate that InSeq analysis detects lung fitness genes conserved in reference strains causing nosocomial pneumonia, pyogenic liver abscess, and carbapenem-resistant infections. ![*K. pneumoniae* conserved genes are fitness factors during pneumonia. (A) The number of genes shared between KPPR1 (orange), pneumonia isolate MGH78578 (green), pyogenic liver abscess isolate NTUH-K2044 (pink), carbapenem-resistant isolate NJST258_1 (blue), and plant endophyte Kp342 (yellow) is shown with the number of genes in each quadrant (labeled by Roman numerals) indicated as calculated by CloVR comparative software. (B) Based on InSeq analysis, 60 of 69 genes with a fitness factor of \>10 were conserved in all five isolates (green), 2 were present in human isolates but not Kp342 (yellow), and 2 were shared with hypervirulent NTUH-K2044 (red).](mbo0031523580008){#fig8} DISCUSSION {#h2} ========== By performing InSeq analysis of *K. pneumoniae* KPPR1, leveraging high-quality genome sequence and a well-established animal model, this study identified over 300 fitness genes important in lung infection. Detection of known virulence genes such as the *wzi* capsule gene validated this approach. Adaptation of CEDER analysis for ranking of fitness genes, based on the concordance of read count ratios from multiple transposon insertions within genes, provided a reliable list of fitness genes that were experimentally validated. These validation experiments demonstrated that aromatic and branched-chain amino acid synthesis pathways, copper efflux, and global virulence gene regulators such as RfaH are critical for *K. pneumoniae* to cause pneumonia. The identification of genes such as *rfaH*, with a profound contribution to lung fitness, indicates the benefit of applying InSeq even when prior forward genetic screens have been performed ([@B6], [@B7]). Enrichment analysis further substantiated amino acid synthesis as central to lung fitness, and comparative genomics indicated that many critical fitness genes are highly conserved in *K. pneumoniae*. The large set of fitness genes in KPPR1 newly identified by InSeq should accelerate progress in defining the virulence strategies of *K. pneumoniae.* Enrichment analysis and experimental validation of InSeq-selected genes indicate that *K. pneumoniae* must synthesize amino acids that the host cannot. Since essential amino acids are acquired through diet, it does not necessarily follow that these amino acids would be limiting in the lung. However, based on measurements in human subjects, the concentrations of these amino acids are significantly lower in pulmonary epithelial lining fluid than in plasma ([@B31]). InSeq identified mutants with decreased fitness in pathways that synthesize the host's essential amino acids histidine (*hisG*); isoleucine, valine, and leucine (*ilvABCDEN* and *leuABC*); methionine/cysteine (*metACBFL*); phenylalanine and tryptophan (*aroE*, *pheA*, and *trpD*); and threonine (*thrBC*) (see [Data Set S2](#dataS2){ref-type="supplementary-material"} in the supplemental material) ([@B32]). This indicates that synthesis of amino acids that are essential to its host is also critical for *K. pneumoniae* to infect the lung. Branched-chain amino acid metabolism may be critical for *K. pneumoniae* lung fitness for two reasons: nutrient limitation and copper toxicity. In contrast to reduced branched-chain amino acid levels, copper is increased in human lungs compared to serum ([@B33]). Our data show that *K. pneumoniae* must synthesize branched-chain amino acids in the lung, but in *E. coli*, this pathway is blocked by copper through its inhibition of dehydratases such as IlvD ([@B30]). In *K. pneumoniae*, the *copA* mutant is exquisitely sensitive to copper but is protected by exogenous isoleucine and valine ([Fig. 7C](#fig7){ref-type="fig"}), consistent with this mechanism of copper toxicity. Sulfonylurea herbicides that inhibit acetohydroxy acid synthase in the branched-chain amino acid synthesis pathway can protect mice from *Pseudomonas aeruginosa* and *Burkholderia pseudomallei* pneumonia, but *K. pneumoniae* is predicted to contain a resistant isozyme ([@B34]). The nine *K. pneumoniae* synthesis genes identified by InSeq (*ilvABCDEN* and *leuABC*) could provide novel targets to block branched-chain amino acid (BCAA) synthesis. In contrast to *ilv* mutants, the *aroE* mutant is not auxotrophic in minimal medium but has reduced fitness in the lung. In *E. coli*, the YdiB quinate/shikimate dehydrogenase can perform the same function as AroE, albeit with lower efficiency ([@B28]). The fact that the *aroE* mutant is susceptible to serum killing suggests a specific defect that affects complement resistance. *Salmonella enterica* aro mutants are also attenuated *in vivo* and are susceptible to serum killing in addition to their auxotrophy ([@B35]). The mechanism for the increased serum sensitivity of the *K. pneumoniae* aroE mutant is unclear. In addition to synthesizing building blocks for replication despite nutrient limitations, *K. pneumoniae* must also evade host defenses to cause disease. Polysaccharide capsule is a critical virulence factor of *K. pneumoniae* that evades complement-mediated killing and opsonophagocytosis. Detection of the capsular assembly gene *wzi* as the most significant fitness gene by InSeq analysis reinforces the critical role of capsule. Phenotypic assays indicate that *rfaH* is important in capsular synthesis and is required for survival *in vivo* and in serum. *S*. Typhimurium and uropathogenic *E. coli* *rfaH* mutants are also severely attenuated in animal models, corresponding to defects in *E. coli* capsular synthesis and LPS synthesis in both ([@B20], [@B36]). RfaH appears to be a critical virulence factor that is conserved among *K. pneumoniae* strains and with other pathogenic *Enterobacteriaceae.* Treatment of *K. pneumoniae* infections has become increasingly challenging due to carbapenem and extended-spectrum β-lactamase resistance ([@B4]). Therefore, novel therapeutic approaches are needed to fight these common and life-threatening nosocomial infections. Targets for antimicrobials should be conserved within a species or a group of closely related species at a minimum, have a low potential for toxicity or disruption of human metabolism, and ideally not have a preexisting resistance mechanism. This study identifies 60 genes that are conserved among diverse representatives of *K. pneumoniae* and have a 10- to 10,000-fold defect when disrupted, and many are in prokaryote-specific functions such as synthesis of amino acids that humans do not make or transcription of polycistronic RNAs (*rfaH*). Through careful study of their function during infection, some of these gene products could be pursued as targets for novel antimicrobials. MATERIALS AND METHODS {#h3} ===================== Bacterial strains and media. {#s3.1} ---------------------------- *K. pneumoniae* KPPR1 ([@B10]) and isogenic mutants were cultured in Luria-Bertani (LB) broth at 37°C with shaking or 30°C on agar (Becton, Dickinson and Company, Sparks, MD) supplemented with kanamycin (25 µg/ml), spectinomycin (50 µg/ml), chloramphenicol (20 µg/ml), and rifampin (30 µg/ml) as indicated. Murine pneumonia model. {#s3.2} ----------------------- Six- to 8-week-old C57BL/6 mice (Jackson Laboratory, Bar Harbor, ME) were anesthetized with isoflurane and inoculated retropharyngeally with 1 × 10^6^ CFU of pooled *K. pneumoniae* transposon mutants. LB broth-grown cultures were centrifuged, resuspended, and diluted in phosphate-buffered saline (PBS) to a concentration of 2 × 10^7^ CFU, and 50 µl of the suspension was administered. After 24 h, mice were euthanized by CO~2~ asphyxiation. To determine bacterial density, lungs and spleens were removed, homogenized in 1 ml PBS, and cultured on LB agar with appropriate antibiotics. To determine competitive indices, mice (at least 4 per group) were infected as described above with 50 µl of a 1:1 mixture of wild-type and mutant *K. pneumoniae* strains in a total inoculum of 1 × 10^6^ CFU. After 24 h, mice were euthanized, lungs were homogenized in 1 ml PBS, wild-type CFU were measured by culture on LB plates supplemented with rifampin, and mutant CFU were measured on LB plates with rifampin and kanamycin. The competitive index was calculated as (mutant lung CFU/wild-type lung CFU)/(mutant inoculum CFU/wild-type inoculum CFU). Transposon library construction and sequencing. {#s3.3} ----------------------------------------------- The transposon library was constructed by conjugation of the pSAM_Cam plasmid, a modified version of pSAM_Ec ([@B37]) containing the chloramphenicol acetyltransferase gene from pKD3 ([@B15]), into KPPR1 (see [Text S1](#textS1){ref-type="supplementary-material"} in the supplemental material for detailed methods). Insertion sequencing (InSeq; Sequence Read Archive ID [SRP051394](http://www.ncbi.nlm.nih.gov/sra/?term=SRP051394)) was performed as previously described ([@B18]). Construction and complementation of mutants. {#s3.4} -------------------------------------------- Lambda Red mutagenesis was performed as previously described ([@B15]). To make electrocompetent cells, *K. pneumoniae* containing the pKD46 plasmid ([@B15]), modified to encode spectinomycin resistance (a gift from Chris Alteri), was cultured overnight in LB broth containing spectinomycin at 30°C with shaking. The following day, cultures were diluted 1:100 in LB broth with spectinomycin and 50 mM [l]{.smallcaps}-arabinose and cultured at 30°C until reaching a reading of optical density at 600 nm (OD~600~) of 0.5 to 0.6 (approximately 4 h). Cultures were placed on ice for at least 30 min and centrifuged in sterile cold bottles at 8,000 × *g* for 15 min at 4°C. The supernatant was decanted, and bacteria were serially washed and centrifuged in ice-cold sterile volumes of 50 ml 1 mM HEPES at pH 7.4 (Invitrogen, Carlsbad, CA), 50 ml distilled water (dH~2~O), and 20 ml 10% glycerol. Pellets were resuspended in ice-cold sterile 10% glycerol at a final density of 2 × 10^10^ to 3 × 10^10^ CFU/ml and stored at −80°C in 50-µl aliquots. To generate null mutants, *E. coli* BW25141 containing the pKD4 plasmid was cultured overnight in LB broth containing 50 µg/ml kanamycin (MP Biomedicals, Santa Ana, CA) at 30°C. The pKD4 plasmid was isolated using a Spin Miniprep kit (Qiagen, Valencia, CA). Oligonucleotide primers were then designed with 60-bp homology flanking the region targeted for deletion added to 5′ ends of P1 and P2 sites of the pKD4 kanamycin resistance cassette (see [Table S2](#tabS2){ref-type="supplementary-material"} in the supplemental material). The targeting fragment was generated by PCR consisting of 95°C for 5 min; 30 cycles of 95°C for 1 min, 58°C for 1 min, and 72°C for 1 min; and 72°C for 5 min. PCR products were pooled and purified using a Qiagen PCR purification kit. PCR products were digested overnight at 37°C with DpnI, and 10 µl was added to the electrocompetent pKD46 cells, gently mixed, and incubated on ice for 10 min. The mixture was electroporated using a 0.1-cm-gap cuvette (Fisher Scientific; catalog no. FB101) at 1.8 kV, 400 Ω, 25 µF, with a Bio-Rad Micropulser (Bio-Rad, Hercules, CA), and cells were recovered with SOC medium and incubated overnight at 30°C with shaking in sterile culture tubes. Next, cells were spun down, resuspended in LB broth, plated onto LB broth plates containing kanamycin, and incubated at 37°C overnight. Transformants were restreaked on LB agar and confirmed by colony PCR using flanking primers (see [Table S2](#tabS2){ref-type="supplementary-material"}). To complement the *rfaH* and *copA* mutants, PCR products containing the open reading frame and upstream sequence (see [Table S2](#tabS2){ref-type="supplementary-material"} in the supplemental material) were inserted into pCR 2.1 by TOPO TA cloning (Life Technologies, Carlsbad, CA) and transferred to pACYC184 by ligation after digestion with Xbal and HindIII. The resulting complementation plasmid or pACYC184 alone was introduced into WT or mutant *K. pneumoniae* by electroporation. Serum growth assay. {#s3.5} ------------------- RPMI medium (Invitrogen, Grand Island, NY), supplemented with 10% (vol/vol) heat-inactivated pooled human serum, was inoculated with 1 × 10^3^ CFU/ml of an overnight culture of *K. pneumoniae* and incubated overnight in a final volume of 100 µl in 96-well plates at 37°C with 5% CO~2~. To determine bacterial density, samples were serially diluted and plated on LB agar (Thermo Fisher Scientific, Waltham, MA) with appropriate antibiotics. Growth curves. {#s3.6} -------------- *K. pneumoniae* strains were cultured overnight in LB broth. On the following day, cultures were incubated in LB or M9 (Invitrogen) medium with or without isoleucine and valine supplementation (Sigma-Aldrich, St. Louis, MO) at a starting density of 2.6 × 10^7^ CFU/ml and cultured for 8 h at 37°C. Absorbance readings at 600 nm were taken every 15 min using an Eon microplate spectrophotometer with Gen5 software (BioTek, Winooski, VT). Capsule staining. {#s3.7} ----------------- *K. pneumoniae* strains were cultured overnight in LB broth. On the following day, 10 µl of culture was added to slides and allowed to air dry. The dried bacteria were then heat fixed to the slide (3 min at 56°C); 10 µl of India ink (Becton, Dickinson and Company, Sparks, MD) diluted 1:3 in PBS was added and wet mounted with a coverslip. Superfrost slides (Thermo Fisher Scientific, Waltham, MA) were viewed and imaged using an Axioplan2 phase-contrast microscope (Zeiss, Irvine, CA) with a SPOT diagnostic camera and software (SPOT Imagine Solutions, Sterling Heights, MI). Mucoviscosity assay. {#s3.8} -------------------- Overnight cultures were pelleted by centrifugation at 9,400 × *g* and resuspended in PBS to an OD~600~ of \~1. The suspensions were centrifuged for 5 min at 1,000 × *g*, and the OD~600~ of the supernatants was measured. Final readings were normalized to the OD~600~ of the wild type before centrifugation. Serum killing assay. {#s3.9} -------------------- *K. pneumoniae* strains were cultured overnight in LB broth. On the second day, cultures were diluted to 2.5 × 10^5^ CFU/ml in non-heat-inactivated human serum and incubated for 3 h at 37°C. Aliquots at *t* = 0 and *t* = 3 h were plated for CFU on LB agar with appropriate antibiotics. Copper sensitivity assay. {#s3.10} ------------------------- Sensitivity to copper was measured by washing 3 ml of stationary-phase cultures twice with PBS and then centrifuging them at 10,000 × *g* and resuspending them in M9 minimal medium. Next, 2-ml reaction mixtures were prepared with defined concentrations of copper sulfate (98% pure; Sigma, St. Louis, MO) in M9 medium with bacterial cultures normalized to an OD~600~ of 0.2. Reaction mixtures were incubated for 18 h at 37°C in six-well plates. Following incubation, CFU were enumerated by quantitative culture. Genome comparison and gene enrichment analysis. {#s3.11} ----------------------------------------------- To identify genes shared between KPPR1 (GenBank identifier \[ID\] [CP009208](CP009208)) and reference *K. pneumoniae* isolates MGH78578 (GenBank ID [CP000647](CP000647)), NTUH-K2044 (GenBank ID [AP006725](AP006725)), NJST258_1 (GenBank ID [CP006923.1](CP006923.1)), and Kp342 (GenBank ID [CP000964](CP000964)), reference genomes were compared by CloVR comparative software (on the DIAG computing platform), generating clusters of genes shared between genomes. The number of genes shared between each genome was tabulated, and a Venn diagram was generated with free R (v.3.1.1) software and the Venn diagram package. To identify biological pathways associated with lung fitness, enrichment analysis was performed using KOBAS 2.0 ([@B38]). Statistical analysis. {#s3.12} --------------------- To quantify the significance of each gene as a potential fitness factor, we first tested the difference in counts between inoculum and lung at each transposon insertion using an exact Poisson test and then combined the insertion-level *P* values into a *P* value for each gene using Fisher's method (using R 3.1.1 software) in a modification of CEDER analysis ([@B19]). A small *P* value indicates an important fitness factor. To test whether the *copA* mutant is more sensitive to copper than the wild type, a linear regression model was used (the relation between log-transformed CFU and Cu concentration is approximately linear). Statistical analysis of CFU data was performed on log-transformed data by a one-sample *t* test for competitive index and a two-sample *t* test or analysis of variance (ANOVA) with Fisher's least significant difference (LSD) test as indicated using Prism 6 (GraphPad Software, La Jolla, CA). Ethics statement. {#s3.13} ----------------- This study was performed in strict accordance with the recommendations in the *Guide for the Care and Use of Laboratory Animals* ([@B39]). The University of Michigan Institutional Animal Care and Use Committee (IACUC) approved this research (PRO00005795). SUPPLEMENTAL MATERIAL {#sm1} ===================== ###### Supplemental methods. Download ###### Text S1, PDF file, 0.1 MB ###### Transposon insertion sites and counts. Download ###### Data Set S1, XLSX file, 2.2 MB ###### Fitness ratio and CEDER analysis of *K. pneumoniae* KPPR1 genes. Download ###### Data Set S2, XLS file, 0.8 MB ###### Gene intersection lists. Download ###### Data Set S3, XLSX file, 0.8 MB ###### pSAM_Cam is suicidal in *K. pneumoniae*, and transposon insertion is random. (a) Relevant features of pSAM_Cam. (b) To verify that pSAM_Cam was suicidal in *K. pneumoniae*, colony PCR was performed using primers that anneal within the plasmid backbone (top) and primers that anneal within the Kan cassette (bottom). The presence of pSAM_Cam generates a 999-bp PCR product from the plasmid backbone and a 1,338-bp product from the Kan cassette. The presence of the transposon-containing Kan cassette inserted into *K. pneumoniae* generates a 1,338-bp product. (c) To assess the randomness of the transposon mutant library, genomic DNA from Rif^r^ Kan^r^ colonies was harvested, digested with EcoRI, and subjected to Southern blotting. The variation in sizes of fragments containing the Kan cassette indicates that the transposon is inserted in a different region of the chromosome for each of the mutants tested. Download ###### Figure S1, TIF file, 0.2 MB ###### The *aroE* and *rfaH* mutants do not have growth defects in M9 or RPMI medium. (A) CFU per milliliter after inoculation with 1 × 10^3^ CFU and overnight incubation in RPMI medium is shown as mean ± standard deviation from two independent experiments. (B) Optical density of *K. pneumoniae* KP4 and isogenic mutants during incubation in M9 minimal medium at 37°C is shown as mean ± standard deviation from triplicate cultures and is representative of three independent experiments. Download ###### Figure S2, TIF file, 0.1 MB ###### Read counts from InSeq analysis. ###### Table S1, PDF file, 0.02 MB ###### Primers used in this study. ###### Table S2, PDF file, 0.1 MB **Citation** Bachman MA, Breen P, Deornellas V, Mu Q, Zhao L, Wu W, Cavalcoli JD, Mobley HLT. 2015. Genome-wide identification of *Klebsiella pneumoniae* fitness genes during lung infection. mBio 6(3):e00775-15. doi:10.1128/mBio.00775-15. This research was supported in part by the University of Michigan Medical School Host Microbiome Initiative. Research using CloVR was conducted on the National Science Foundation funded MRI-R2 project \#DBI-0959894. We thank Victoria Holden for assistance with bacterial plating, Sargurunathan Subashchandrabose for scientific discussions about the project, the University of Michigan DNA Sequencing Core for consultation and Illumina HiSeq sequencing, and the Center for Live Cell Imaging for microscope training and access.
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Scientists Just Made The World's Thinnest Hologram An Australian-Chinese research team has created the world's thinnest hologram, paving the way towards the integration of 3D holography into everyday electronics like smart phones, computers and TVs. Interactive 3D holograms are a staple of science fiction – from Star Wars to Halo­­ (all the space things, really) - but the challenge for scientists trying to turn them into reality is developing holograms that are thin enough to work with modern electronics. Now a pioneering team led by RMIT University’s Distinguished Professor Min Gu has designed a nano-hologram that is simple to make, can be seen without 3D goggles and is 1000 times thinner than a human hair. Gu says integrating holography into everyday electronics would make screen size irrelevant – since a pop-up 3D hologram can display a wealth of data that doesn't neatly fit on a phone or watch. "From medical diagnostics to education, data storage, defence and cyber security, 3D holography has the potential to transform a range of industries and this research brings that revolution one critical step closer," says Gu. Conventional holograms modulate the phase of light to give the illusion of three-dimensional depth. But to generate enough phase shifts, those holograms need to be at the thickness of optical wavelengths. The RMIT research team, working with the Beijing Institute of Technology (BIT), has broken this thickness limit with a 25 nanometre hologram based on a topological insulator material – a novel quantum material that holds the low refractive index in the surface layer but the ultrahigh refractive index in the bulk. The topological insulator thin film acts as an intrinsic optical resonant cavity, which can enhance the phase shifts for holographic imaging. Dr Zengyi Yue, who co-authored the paper with BIT’s Gaolei Xue, said the next stage for this research will be developing a rigid thin film that could be laid onto an LCD screen to enable 3D holographic display. This involves shrinking othe nano-hologram's pixel size, making it at least 10 times smaller. "But beyond that, we are looking to create flexible and elastic thin films that could be used on a whole range of surfaces, opening up the horizons of holographic applications," says Yue. Gizmodo Australia is gobbling up the news in a different timezone, so check them out if you need another Giz fix.
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Chloroplast movements in leaves: Influence on chlorophyll fluorescence and measurements of light-induced absorbance changes related to ΔpH and zeaxanthin formation. Light-induced chloroplast movements were found to cause changes in chlorophyll fluorescence emission, closely matching those in leaf absorptance, both in terms of the kinetics and the maximum extent of the changes observed in different species. The results demonstrate that chloroplast movements can have a significant effect on the efficiency of light utilization in photosynthesis. They further show that chloroplast movements need to be taken into account in measurements of fluorescence quenching and especially in measurements of light-induced optical changes used to monitor zeaxanthin formation and ΔpH associated light scattering in leaves. Means of minimizing and of adjusting for the influences of chloroplast movements in such measurements are discussed.
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Measurements of selected thermoregulatory responses to heating and cooling the rostral brainstem of four classes of vertebrates (fish, reptiles, birds and mammals) will reveal characteristics of the central neurons that have evolved to respond to thermal stress. These characteristics are derived from the thresholds and slopes of the response curves versus hypothalamic temperature. From these curves obtained in resting, waking, exercising, sleeping, afebrile and febrile animals exposed to environments ranging from hot to cold, important deductions can be drawn regarding the neurons that coordinate peripheral and central thermal information and then activate appropriate thermoregulatory responses. Measurements of selected osmoregulatory responses to heating and cooling the rostral brainstem and to perfusing hyper-and hypotonic solutions into the rostral brainstem of penguins will yield information about the neurons which induce water intake and salt secretion by the salt glands of marine birds. Water intake and urine formation in dogs in response to osmotic stimulation while subjected to varying degrees of hydration and salt loading will yield comparable information about the characteristics of the osmoreceptors in mammals.
3.171875
3
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Q: Power of an engine Suppose a car of mass $m$ starts out with an acceleration $a$ in the positive direction (say +ve x-axis), against a constant Resistive force $R$. At the instant it's velocity is $v$, what is power of engine? The answer is $(R+ma)v$ which is intuitive as the engine is working against two forces, but the net Force is $ma - R$, so why isn't power $F_{net} v = (ma-R)v$? A: The engine does work to overcome friction and increase the kinetic energy of the car. Let the power developed by the engine be $P=F_{\rm engine}v$. $Rv$ of that power $P$ is the rate of working against the frictional force. The rest of the power developed by the engine is the rate of working to accelerate the car (increase its kinetic energy) which has a net force $F_{\rm net}(=ma)$ on it and so is equal to $F_{\rm net}v=mav$ So $P=F_{\rm engine}v= Rv + F_{\rm net}v=Rv+mav$ noting that $F_{\rm engine}= R + F_{\rm net}\Rightarrow F_{\rm engine}-R = F_{\rm net}$
3.65625
4
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Gastroesophageal reflux in athletes. Gastroesophageal reflux (GER) and its associated symptoms are common among athletes. In the athlete, GER increases with intensity of exercise, is more common with endurance sports, and worse with postprandial exercise. GER has symptoms that overlap with other upper gastrointestinal (GI) conditions. Symptoms of GER can be difficult to distinguish from cardiac chest pain. GER may exacerbate asthma. Proposed mechanisms causing GER during exertion include altered GI blood flow and motor function, neuroendocrine changes, and mechanical effects. GER symptoms that interfere with activity may respond to lifestyle modification or pharmacologic therapy.
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The Fukushima nuclear crisis certainly had profound implications for Japan. In November 2013, Japan’s lower house and upper house successively passed legislation to start electricity sector reform in 2015. Nuclear energy, which used to account for 30 percent of Japan’s electric power, was discarded after the earthquake and Fukushima incident, leading to energy price hikes (see graph below). The new bill, designed to break up monopolies, curb electricity prices and facilitate the development of renewable energy through a series of liberal reforms, is the child of the Fukushima nuclear crisis. Source The reform plan consists of three stages. The bill in question provides the legal background for the first stage of reform – the creation of a national grid company in 2015. This entity, after merging different regional grids, will be authorized to instruct power companies to supply electricity to each other when needed to overcome supply shortages. This reform emphasizes electricity transfer among regions, making sure that power shortages during the Fukushima incident would not happen again. Related article: Here's An Official Vote For Nuclear The second and third stages of reform seek to liberalize the sale of electricity to households and strip the major power firms of power transmission and distribution functions. The new bill’s supplementary provision included a plan to enact bills in 2014 and 2015 to stipulate these steps of reform. The logic of the reforms is straightforward. The 10 regional electricity companies have monopolized Japan’s regional electricity markets for over half a century: they have total control of power generation, transmission and retail in their own regions. Users cannot choose their electricity supplier from other regions. Now, 98 percent of Japan’s electricity supply comes from those big corporations. Unfortunately, they all face soaring costs for imported fuel, which lead to electricity prices that are twice as high as those in the U.S. By allowing households to choose electricity providers and ensuring renewable energy’s access to the national grid, Japan’s electricity sector is expected to see higher supply with more competition. “Consumers will have a wider choice over the purchase of electricity from operators and in terms of fees. It will also lead to a reduction in electricity payments,” said Toshimitsu Motegi, minister of the economy, trade and industry. In any political scenario, the greater the perceived impact, the fiercer the opposition you will face. Japan’s regional electricity companies and the opposition parties tried hard to kill the legislation. In June 2013, Abe’s cabinet submitted a bill to the Diet, deliberation on which was postponed for an unrelated political reason. Similar stories have unfolded multiple times since 1990s, when Japan’s leaders tried to revamp the electricity sector. Luckily, this time, due to the Fukushima crisis, the power companies lost public support. Therefore, the first stage of reform, a unified national grid that guarantees power supply during emergencies, was passed this time without further delays. However, whether this series of reforms can achieve lower electricity prices for households and corporations remains to be tested. What is certain is that old monopolies will face challenges from new energy providers and pressure to improve their services and prices. Renewable energy providers will have a bigger stake in Japan’s electricity market. On the other hand, we are not yet sure whether the opposition forces will fight to the death to stall the next steps of the reform or not. By Roger Yu Du
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The Role and Functions of a County Governor in Kenya The role and functions of a County Governor in Kenya are diverse. One of the most important elective positions in Kenya is that of a county governor. The County Governor in Kenya is the head of the county government, which is the second level of government. The other level of government is the national government. Article 1 of the Constitution delegates the sovereign power of the people to the County Governments as state organs. The county governments can also exercise this power at the county level. A County Governor in Kenya is a democratically elected representative who exercises this power indirectly at the county level. Kenya has 47 county governments, which translates to 47 governors. The county governor is the chief executive of the county and the head of the county executive committee. The members of the county executive committee answer to the governor while performing their functions (Article 179 (6)). Let us now look at the role and functions of a County Governor in Kenya. Powers of the County Governor in Kenya The County Governments Act contains the powers of the County Governor. Section 31 of the Act designates the following powers to the governor. The governor can dismiss a county executive member at any time if he or she considers it appropriate or necessary. Second, the governor could dismiss a county executive member following a resolution passed by the County Assembly (Section 40). However, the High Court declared this section unconstitutional and the Senate is yet to amend the Act to accommodate the ruling. The governor can appoint an accounting officer for each county department, entity, or decentralized unit of the county government. These accounting officers are the Chief Officers who head the different county departments (e.g. Chief Officer in charge of Agriculture, Health, etc.). Lastly, the governor has the powers necessary to execute the duties of the office of the county governor. Functions of the County Governor in Kenya Section 30 (2) of the County Governments Act stipulates the functions of the governor. The county governor should: execute the functions diligently and exercise the authority that the Constitution and the law provides; perform State functions within the county that the President may assign from time to time on the basis of mutual consultations; represent the county in national and international fora and events; appoint, with the approval of the county assembly, the county executive committee in accordance with Article 179(2)(b) of the Constitution; come up with the portfolio structure for the county executive committee to respond to the functions and competencies that the law assigns and transfers to each county. submit the county plans and policies to the county assembly for approval; consider, approve and assent to bills that the county assembly passes; chair the meetings of the county executive committee; by a decision notified in the county gazette, assign to every member of the county executive committee responsibility to ensure the performance of any function within the county and the provision of related services to the people. submit an annual report to the county assembly on the implementation status of the county policies and plans; deliver the annual state of the county address containing such matters county laws may specify; and sign the notice of all important formal decisions made by the governor or by the county executive committee, and ensure they are published in the county gazette. Responsibilities of the County Governor in Kenya In performing the functions stated above, the county governor should: provide leadership in the county’s governance and development; provide leadership to the county executive committee and administration based on the county policies and plans; promote democracy, good governance, unity and cohesion within the county; promote peace and order within the county; advance the competitiveness of the county; be accountable for the management and use of the county resources; and promote and facilitate citizen participation in the development of policies and plans, and delivery of services in the county. Would you like to share your thoughts on this topic? Let me know in the comments below!
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Core making generally involves mixing sand with a binder that sets by chemical action (cold cure method) or by heat (hot-box method). The cold cure processes have proved commercially successful because of their speed and core strength achievable without the need for thermal energy. However, the noxious and contaminating characteristics of the curing gas for cold cure resins have been a considerable draw back. With respect to the hot box type, one process stands out in this regard because the chemicals employed are relatively free from noxious odors and the chemical system is responsive to thermal energy which can be generated by microwaves. This hot box system employs a water soluble inorganic binder, such as sodium and potassium silicates, which while it can be cured either by CO.sub.2 gas or esters, it can also be cured by heat. The concept of using microwave energy to cure sand mixtures for core making is known. However, in spite of the general state of the art with respect to microwave technology, several problems remain to be solved with respect to making better quality cores which can be employed in aluminum semi-permanent molding. These problems fall into basically two categories, (1) the rapidity of heating with microwave energy causes uncontrolled rapid expansion of gases within the sand core leading to cracking, (2) uneven heating and curing of the core sand mixture may result from unusual core configurations and from reliance solely on molecular friction of the resin to do the heat curing, and (3) microwaved sand cores have an unusual tendency to absorb moisture during storage which eventually destroys their desired strength characteristics, and (4) lack of a uniform gradient of curing to insure proper strength and at the same time provide easy shakeout of the sand grains. Accordingly, it is important that there be improved molecular polar heating of the water-resin solution within the sand mixture without experiencing extremely rapid vapor generation and with improved heat transfer from the surrounding core box to insure a uniformity of curing gradient, and that there be some mechanism to reduce hygroscopic tendencies of the core.
3.03125
3
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Umvolkung Umvolkung () is a term in Nazi ideology used to describe a process of assimilation of members of the German people (the Volk) as a way for them to forget about their language and their origin. As a neologism, it echoes Umpolung 'polarity inversion', leading to an interpretation akin to "ethnicity inversion". The term is also used to describe the "re-Germanisation" of the German people, after new Lebensraum was conquered and the German people who already resided there would become more German again. Umvolkung in the first sense was seen as a negative process during the Third Reich, while the second process was seen as more desirable. Origin and background The term was invented by Albert Brackmann, a leader of the Ostforschung, which was a research organization that investigated the character and the attitudes of people (the so-called "Verhalten") living in areas east of the German Reich, e.g. in Poland, Ukraine, Slovakia and Romania. There was a plan to conquer almost the whole of Eastern Europe and process the "Umvolkung", so that all the former German people who had slowly assimilated and mixed with the other ethnicities, would become more German again. Use of the word today The term became a catchphrase and is often used to describe the German peoples fear of Überfremdung by immigrants or their descendants, who have seen an increase in population since the foundation of the German Federal Republic. In this use, it has largely become synonymous with the "Great Replacement" and the white genocide conspiracy theory. See also Lebensraum Generalplan Ost Germanisation Xenophobia Volk Glossary of Nazi Germany References http://www.doew.at/projekte/rechts/chronik/1998_07/umvolker.html Category:Nazi terminology Category:Cultural assimilation Category:German words and phrases
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Where do these early differences come from? A growing body of evidence suggests that a huge influence on early language development is the number of words that children hear as infants and toddlers. The more that parents speak to their infants and in front of their infants, the better infants get at understanding speech and learning words. This issue has been explored in some previous work that has compared children who grow up in low socioeconomic status (SES) and high SES homes. An interesting paper in the November, 2013 issue of Psychological Science by Adriana Weisleder and Anne Fernald examined this question just within a sample of low SES Spanish speaking homes in the United States. They had 19-month-old infants wear an audio recorder for at least one full day. Many infants wore the recorder for several days, and the longest recording day was selected. Using software, the recordings were analyzed to identify all of the words spoken in the infants’ presence during that day. In addition, the researchers classified the speech by whether it was directed at the infants or whether it was just speech that the infants overheard. Both when the infants were 19-months-old and again when they were 24-months-old, the researchers measured their efficiency at understanding speech. In these tests, the infants were seated in front of a screen. They saw pairs of pictures displaying common objects (like a dog or a ball). They heard the Spanish word for one of those pictures spoken and the researchers measured how much the infant looked at the picture corresponding to the spoken word as well as how quickly the infant looked at that picture after the word was spoken. In addition, at 24 months, the parents used a checklist to estimate the size of their child’s vocabulary. Within this sample, there was a huge difference in the number of words that the infants heard. Some infants heard fewer than 2000 words in a day, while some heard over 15,000. In addition, there were big differences in child-directed speech. Some families spoke fewer than 1000 words to their children in a day, while others spoke over 10,000 words to their children. The number of words spoken to children at 19 months was a significant predictor of the child’s vocabulary at 24 months. In addition, the number of words spoken to children predicted how quickly and effectively children looked at the picture associated with a word they heard. Statistical analysis demonstrated that the ease of identifying the words in speech was an important reason why infants who heard more words had a larger vocabulary at 24-months than infants who heard fewer words. This early language experience compounds itself over time. Not only do infants who hear lots of words understand language better than those who hear fewer words, they are also more likely to start vocalizing and speaking words earlier. When children talk more, adults talk back to them more often. So, the early advantage in language ability gets bigger over time. This research demonstrates the importance of a rich environment for infants. Infant brains are developing rapidly, and that brain development is strongly influenced by what is going on around them. The more that these infants are embedded in a complex language environment, the more that their language abilities develop. And that early development gives them a huge advantage as they start school. Follow me on Twitter. And on Facebook and on Google+. Check out my books Smart Thinking and Habits of Leadership And coming in January, 2014, Smart Change. Listen to my new radio show on KUT radio in Austin Two Guys on Your Head and follow 2GoYH on Twitter.
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Q: what does the mean of base-b exactly? i know how to convert from base b to decimal but Im not understand what is base-b exactly. I know we multiply the base to the numbers if we gonna convert to bas 10 then multiply with then is base-b(base 5)? A: In order to follow this, we should understand the difference between a number and its representation. Let's start with the (natural) numbers. There are two special numbers: zero and one. Zero is the neutral element of addition (i.e. you can add zero to anything without changing it) and one is the neutral element of multiplication. Every other number can be induced by these two numbers. Start with zero. Then, subsequently add one. A common representation for numbers is the decimal system. However, this is purely arbitrary and any other system could be used as well. There is nothing intrinsic in the number twelve that would require us to write it as 12. The nice thing is that all arithmetic rules are defined on the numbers themselves, not on their representations. Five plus six will always be eleven. No matter how you represent them. You may have already noticed that I use number words when I talk about the numbers and any other representation if I talk about the representation. Ok, so we have our numbers. Now we need a way to represent them. Imagine we have three symbols a, b, and c. We could just assign the first three numbers to them a (zero) b (one) c (two) But then we are out of symbols. As you know, the positional numeral systems solve this by introducing another position. Then, just continue as before. Assign the next few numbers in order ba (three) bb (four) bc (five) ca (six) cb (seven) cc (eight) You might want to continue with a third position: baa (nine) bab (ten) bac (eleven) ... The base of this system is three (or ba) because we have three symbols. We can observe that the digits in the second position stand for an addition of a multiple of three (b. stands for three + ., c. stands for two times three + . ...) Expressed in base ba, this is: b. = b * ba + ., c. = c * ba + .. This continues to all positions and you can generalize that a number formed of digits dn ... d1 d0 can be expressed by the well-known formula: n = Sum(i) di * base^i The intuition behind this formula is that there will be base numbers with one digit, base^2 numbers with two digits and so on. And the di * base^i term skips the first few of them (as many such that the first digit matches, then the second and so on). We can check this at the example of bac which should be eleven: n = b * ba^c + a * ba^a + c * ba^a = one * three^two + zero * three^one + two * three^zero = nine + zero + two = eleven = bac Remember that the arithmetic rules apply to the numbers and not to the representations? So since we know the definition of our number (second line in the above formula), we can use any other number representation. For example, the decimal one: n = one * three^two + zero * three^one + two * three^zero = 1 * 3^2 + 0*3^1 + 2*3^0 = 9 + 0 + 2 = 11 (decimal) But we could also use another base, e.g. base-8: n = one * three^two + zero * three^one + two * three^zero = 1 * 3^2 + 0*3^1 + 2*3^0 = 11 + 0 + 2 = 13 (octal) So basically, these systems arise naturally by assigning digit sequences systematically to subsequent numbers. The conversion is so simple because the positional equation applies to the numbers, not to the representations. I hope this answer was not too abstract and helped you.
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Even though glyphosate is used to control weeds in agricultural fields, the world's most commonly used weedkiller has also been detected in streams, rivers and other aquatic systems worldwide due to runoff. As we learn more and more about the potential environmental risks of glyphosate runoff, in Brazil—where almost 188,000 tons of glyphosate was sold in 2013 alone—new research published in the peer-reviewed journal Phycologia found that all-important macroalgae is sensitive to glyphosate exposure, even at legal levels. According to the study, the herbicide can alter the photosynthesis, chlorophyll levels and respiration of these key freshwater organisms. Macroalgae play a crucial role in aquatic systems. As a press release for the study pointed out, these organisms help monitor the health and clarity of rapidly moving fresh water. In streams, they cycle nutrients and help increase plankton. For the study, the authors tested several concentrations of Monsanto's glyphosate-based Roundup and aminomethylphosphonic acid (AMPA; the main degradation product of glyphosate) on green algae samples collected from a stream in southwestern Brazil. The green algae tested, Nitella microcarpa var. wrightii, is commonly found in streams around the world. As Sustainable Pulse reported from the study: The authors found that glyphosate + surfactants (Roundup) strongly reduced algal photosynthesis. According to author Ciro Cesar Zanini Branco, "Such effects are related to the concentration of the active ingredient and also to the exposure time. These impacts were observed even at the concentration levels allowed by Brazilian regulations." In contrast, AMPA boosted photosynthesis. Dark respiration, or respiration that occurs regardless of light, also increased with AMPA treatment. Finally, the current study found less chlorophyll when AMPA and certain amounts of solely glyphosate were applied." "Clearly," as the press release stated, "the performance of the algae was affected by the herbicides." "The form of the herbicide (glyphosate, glyphosate plus Roundup or AMPA) is crucial in determining the intensity of the effects, which means that algal productivity could shift visibly depending on the types of herbicides applied to agricultural land near a stream—even if farmers are using them legally," the release continued. Significantly, the authors stressed, even legal concentrations of Roundup in Brazilian waters "may present significant environmental risks": "One of the most dramatic findings of this study is that a significant reduction in photosynthetic rate of N. microcarpa var. wrightii was observed (−42.1 percent) even at the lowest Roundup concentration tested (0.28 mg l−1). Considering that 0.28 mg l−1 is the maximum concentration of this herbicide allowed by Brazilian law in water used for irrigation and animal consumption (National Environmental Council 2005) and the occurrence of glyphosate in the environment (Coupe et al. 2012; Majewski et al. 2014), this result suggests that even legal concentrations of Roundup in water bodies commonly used for these activities (e.g. low-order streams and small lakes) may present significant environmental risks." Even though glyphosate contamination has been detected in the waters of the U.S., Canada, France, Argentina and other countries, the authors of the current study noted that there has been no prior research on the effects of glyphosate on macroalgae. "This paper provides an important contribution to our knowledge of the environmental toxicology of glyphosate-based herbicides in freshwater aquatic systems," said Phycologia editor David Garbary. Dr. Nathan Donley, a scientist at the Center for Biological Diversity, told EcoWatch that the Brazilian study "adds to the body of literature that glyphosate in combination with other ingredients can be more harmful than just glyphosate by itself." Donley, who was not involved in the current study, observed that the environmental health risks of glyphosate merits attention. "A lot of the recent focus on glyphosate has been on human cancer, but it's important to realize that this is not only a carcinogen but also a toxin that is harmful to our natural ecosystems," he said. The World Health Organization's International Agency for Research on Cancer linked glyphosate to cancer last year. "Glyphosate is extremely toxic to plant life and these effects can have serious consequences for other organisms as well," he said. "We've been seeing glyphosate killing milkweed all over the country and having serious unintended consequences for the Monarch butterfly. It is still unknown how these effects on macroalgae could be effecting changes in stream ecosystems." "The problem is that the [Environmental Protection Agency] is still stuck in this fairytale world where chemicals are encountered in isolation and that is not an accurate reflection of how exposure occurs. 'Inert' ingredients are not inert, they have activity and they can change the toxicity profile of the active ingredients and can also have toxicities themselves," Donley concluded.
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1. Field of the Invention The invention relates generally to detecting a biomolecular binding event and more particularly to detecting such events using spectroscopy. 2. Background Information Many current methods for detecting disease or the risk of developing a disease rely on detection of one or more biomolecular interactions between a target molecule in the biological sample and a detectable probe molecule. The probe molecule is typically detectable because it is bound to a detectable label. For example, infection in a subject caused by an infectious agent, such as a virus, can be detected by detecting binding of a labeled antibody probe to a viral protein. A plethora of bioassays have been developed based on this general concept. Some more recent methods for detecting disease rely on the detection or determination of a nucleic acid sequence in a test sample. Sequence-selective detection of nucleic acid molecules has become increasingly important as scientists unravel the genetic basis of disease and use this new information to improve medical diagnosis and treatment. Nucleic acid hybridization assays are specific biomolecular binding assays that are commonly used to detect the presence of specific nucleic acid sequences in a sample. For example, an infectious agent can be detected by detecting hybridization of a labeled nucleic acid probe to a nucleic acid of the virus. Alternatively, the method can base disease detection on detection or determination of all or a part of the patient's own nucleic acid sequences. For example, a patient's risk for developing a disease can be determined by detection of a genetic mutation. Like other methods that detect biomolecular interactions, nucleic acid hybridization assays typically utilize a labeled probe. Traditionally, radioisotopes have been used as labels. More recently, fluorescent, chemiluminescent and bioactive reporter groups have been used. However, the inclusion of labels in an assay often makes it more expensive and complicated, and increases the background signal of the assay. Hybridization assays can be used not only to detect the presence of a nucleic acid molecule, but determine the sequence of the nucleic acid molecule as well. Traditional approaches for sequence determination utilize the synthesis of labeled nucleic acids that are terminated at one of the four nucleotides. However, these methods are relatively slow and expensive. More recently, methods have been developed that entail synthesizing oligonucleotides on a glass support and effecting hybridization with radioactively or fluorescently-labeled test DNA, and reconstructing nucleotide sequence on the basis of data analysis (E. Southern et al., PCT/GB 89/00460, 1989). A device for carrying out such methods includes a supporting film or glass plate and an array of nucleotides covalently attached to the surface thereof. The array includes a set of oligonucleotides of desired length that are capable of taking part in a hybridization reaction. The sequencing-by-hybridization method discussed above, although providing a less-expensive method with higher-throughput, has certain disadvantages. For example, it typically requires labeling of sample or probe nucleic acids. As discussed above, this increases the cost and complexity of the method and increases background values, thereby decreasing sensitivity. Furthermore, inclusion and detection of labels lowers the throughput of the assay. In an attempt to determine nucleic acid sequences information more efficiently, ultraviolet/visible/near-infrared spectroscopy has been used to directly detect hybridization. Although this type of spectroscopy has successfully detected events for smaller molecules (e.g., CO2), it failed to provide the desired level of efficiency and accuracy for biomolecules, which tend to be larger. The frequency shift in the vibration spectrum that is experienced by larger biomolecules (e.g., DNA) upon binding is too small to be accurately and efficiently detected by UV/visible/near-infrared spectroscopy. Furthermore, the UV/visible/near-infrared radiation causes the molecules to fluoresce, creating background noise that interferes with spectrum signals. Further, the method requires multiple gratings of strong dispersion to resolve the small frequency change, making the optical instrument too bulky for convenient use.
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Introduction ============ Asthma is the most frequent chronic respiratory disease, affecting more than 300 million people around the world ([@B1]). This heterogeneous disease is classified into allergic and nonallergic types, which share common symptoms. Generally, extrinsic irritants such as tobacco smoke, plant pollen, animal fur, dust mite feces, some kinds of food, exhaust fumes, or certain chemicals stimulate allergic asthma in genetically predisposed individuals, whereas nonallergic or intrinsic asthma is usually triggered by infections and physical or emotional stress ([@B2]). In contrast to the relatively stable prevalence of nonallergic asthma of around 3.4%--3.8%, the prevalence of allergic asthma increased from 5.0% in 1996 to 6.0% in 2006 and 7.3% in 2016 ([@B1]). Asthma results from a complex interaction between multiple genes and environmental factors. So far more than 100 candidate genes and single nucleotide polymorphisms (SNPs) are reported to be associated with asthma ([@B3]). Familial aggregation of asthma with a higher concordance between monozygotic twins (0.74) than dizygotic twins (0.35), indicates the presence of a strong genetic influence in the induction of asthma ([@B4]). In 2002, *ADAM33*(disintegrin and metallopro-teinase domain-containing protein 33) was reported to be a genetic risk factor for susceptibility to asthma ([@B5]). The *ADAM33*gene comprises 23 exons extending through a 14-kb segment on chromosome 20p13 and encodes a membrane-anchored metalloprotease which may exert its main effect by processing other molecules, e.g., growth factors and cytokines, linked to airway remodeling ([@B6]). In addition to the membrane-bound molecule, secreted and intracellular isoforms can be produced as further splice variants. Variants lacking the metalloproteinase domain have also been reported which may mediate other activities of the molecule. *ADAM33* gene polymorphisms may affect the fate of *ADAM33* transcripts through their effects on mRNA splicing, mRNA stability, and the selection of transcripts for export to the cytoplasm ([@B7]). *ADAM33* is known to be involved in branching morphogenesis in the fetal lung, and polymorphic variations in this gene are associated with the pathophysiology of chronic obstructive pulmonary disease, airway remodeling, and hyperresponsiveness in asthma ([@B8]-[@B10]). Because the strength of association between asthma and different SNPs in the *ADAM33* gene was reported to vary in different populations, the aim of the present study was to investigate the association between four *ADAM33* SNPs and susceptibility to asthma in a sample of patients from southwestern Iran. Materials and Methods ===================== ***Patients and controls*** The participants were patients who were referred to allergy clinics affiliated with Shiraz University of Medical Sciences (Fars province, southwestern Iran) with a diagnosis of asthma according to Expert Panel Report 3 criteria ([@B11]). The study protocol was approved by the Ethics Committee of our university, and 150 patients with mild to moderate persistent asthma were included in the study after written informed consent was obtained from patients or their parents. Patients with any underlying disease except asthma were excluded from the study. Information was recorded about demographic characteristics, cigarette smoke exposure, family history of atopy and concomitant involvement of allergic rhinitis, atopic dermatitis, and urticaria. By public announcement, a total of 149 age- and sex-matched (±1 year) unrelated healthy volunteers of the same ethnicity as the patients and with no personal or family history of asthma or other atopic diseases, were recruited as a control group and offered free screening for asthma. Blood samples (1 ml) for genetic analysis were obtained from patients and controls with EDTA as an anticoagulant. ***Pulmonary function tests*** Pulmonary function tests were performed by spirometry (Cosmed, Rome, Italy) on patients older than 6 years. Forced vital capacity (FVC), forced expiratory volume in 1 second (FEV~1~), ratio of forced expiratory volume in 1 second to forced vital capacity (FEV~1~/FVC) and peak expiratory flow (PEF) were measured, and spirometry indices \<80% of the predicted values were considered abnormal ([@B12]). ***Genotyping of ADAM33 SNPs*** Genomic DNA was extracted from 200 µl of blood with a DNA extraction kit (GeNet Bio, Nonsan, South Korea) and four SNPs in the *ADAM33* gene previously reported to be associated with asthma in some populations ([@B5],[@B13]) were analyzed with a polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method ([Table 1](#T1){ref-type="table"}). The polymorphic sequence-containing regions were amplified by PCR in a total volume of 25 μl containing 30 ng genomic DNA, 12.5 μl 2x master mix (Ampliqon, Odense, Denmark) and 0.5 μmol of each primer (Bioneer, Daejeon, South Korea). Cycling conditions were as follows: one cycle at 95 ^°^C for 5 min, 30 cycles at 95 ^°^C for 30 sec, 62 ^°^C for 30 sec, 72 ^°^C for 30 sec, and a final extension at 72 ^°^C for 10 min. PCR products were digested with related restriction enzymes (Thermo Scientific, Waltham, MA, USA) according to the manufacturer's protocol, and digested products were then resolved on 2.5% agarose gel. ***Statistical analysis*** Allele, genotype, and haplotype frequencies of *AMAM33* gene SNPs were calculated using Arlequin v. 3.1 software. Linkage disequilibrium (LD) among SNPs in healthy controls and Hardy-Weinberg compliance were analyzed using Haploview v. 4.2 software. Allele and genotype frequencies were compared between patients and controls -- globally and after stratification based on age, sex, and both -- using the chi-squared test, and odds ratios (OR) with a 95% confidence interval (CI) were calculated using Epi-info v. 7 software. Relationships between allele and genotype frequencies in each SNP and each spirometry parameter (based on a cut-off value of 80%), cigarette smoke exposure, family history of atopy, or concurrent involvement of other allergic diseases were also analyzed with the chi-squared test. Values of *P*\<0.05 were considered statistically significant. Results ======= The demographic and clinical characteristics along with the spirometry results in patients with asthma are shown in [Table 2](#T2){ref-type="table"}. Allele, genotype, and three-loci haplotype frequencies of the *ADAM33*gene SNPs in patients and healthy controls are summarized in [Table 3](#T3){ref-type="table"}. There were no differences between patients and controls in allelic or genotype frequencies of the SNPs, even after data stratification based on age, sex, and both. We found no associations between allelic or genotype distribution of the SNPs and spirometry indices, family history of atopy, concomitant involvement of other allergic diseases, or exposure to cigarette smoke. All SNPs met the criteria for the Hardy-Weinberg equilibrium except for rs511898 ([Table 4](#T4){ref-type="table"}). This SNP was omitted from subsequent linkage and haplotype analyses ([@B14]). The results of linkage analysis for the three remaining SNPs showed a linkage between rs2280089 and rs2280091 ([Figure 1](#F1){ref-type="fig"}). The results of haplotype analysis revealed that H5 (0.68%) was observed exclusively in patients, whereas H6 (4.8%), H7 (2.5%), and H8 (1.9%) were seen only in healthy controls. The frequency of H2 and H3 haplotypes were significantly higher in patients than controls (25.65% vs. 14.75%, *P*=0.00046 and 16.65% vs. 7.11%, *P*=0.00013, respectively), and inheritance of these haplotypes was associated with higher risk of asthma up to 2--3 folds. Haplotype H4 was more frequent among controls than patients (8.1% vs. 1.68%, *P*=0.0001) and inheritance of this haplotype was associated with decreased risk of asthma about one fifth in patients ([Table 3](#T3){ref-type="table"}). Discussion ========== Asthma is a chronic inflammatory disorder characterized by obstruction of the bronchial tubes and airway remodeling with increased smooth muscle mass, fibroblast activation, neovascularization, and epithelial alterations. *ADAM33* is preferentially expressed in airway fibroblasts and smooth muscle cells in patients with asthma. ###### ADAM33 gene SNP genotyping by PCR-RFLP: primers, restriction enzymes, and length of the digested product fragments --------------------------------------------------------------------------------------------------------------------- **ADAM33 SNP** **Primer sequences** **Restriction**\ **Recognition site** **Fragment size (bp)** **enzyme** ------------------ -------------------------- ------------------ -------------------------- ------------------------- T+1 (rs2280089)\ F: AGGGTCTGGGAGAAATGGTG\ MboII ...GAAG**A**(N)~8~↓...\ GG: 424+132 bp\ (intron 20) R: TCTTTGGAAGCTGAGCGATG ...CTTCT(N)~7~↑... AG: 424+132+123+301 bp\ AA: 301+132+123 bp T1 (rs2280091)\ F: GTGAATATGGTCAGCAGGAG\ NcoI ...C↓C**A**TGG...\ GG: 375 bp\ (exon 20) R: GTGACTTGGAGCAGATGG ...GGTAC↑C... GA: 375+187+188 bp\ AA: 187+188 bp S1 (rs3918396)\ F: GTGGCAGCATGGACAGT\ BtsCI ...GG**A**TGNN↓...\ GG: 304 bp\ (exon 19) R: CAGGAGTAGGCTCAGGAAG ...CCTAC↑NN... GA: 304+153+151 bp\ AA: 151+153 bp F+1 (rs511898)\ F: AAATACGACTCGAGGC\ BsmBI ...**C**GTCTC(N)~1~↓...\ TT: 220 bp\ (intron 6) R: GGACTTCTCAACCCACGAG ...GCAGAG(N)~5~↑... TC: 220+183+37 bp\ CC: 183+37 bp --------------------------------------------------------------------------------------------------------------------- ###### Demographic and clinical characteristics of patients with asthma ------------------------------------------------------------------------------------------- Age (year) \<13 (n=44) ≥13 (n=106) ------------------------------ --------------- ------------- --------------- -------------- Sex Female (n=22) Male (n=22) Female (n=68) Male (n=38) Mean age±SD (years)\ 8.95±2.44\ 8.27±2.34\ 44.17±16.52\ 39.01±19.39\ (Age range) (5 to 12) (5 to 12) (13 to 82) (13 to 82) Family history 9 12 29 23 Cigarette smoke exposure 19 14 38 11 Concurrent allergic diseases Allergic rhinitis 12 12 33 29 Eczema 18 14 9 10 Urticaria 16 12 16 9 Spirometry parameters FEV~1~ \<80% 4 6 34 22 FVC \<80% 4 9 35 20 FEV~1~/FVC \<80% 0 0 3 4 PEF \<80% 8 12 45 24 ------------------------------------------------------------------------------------------- ###### Allele, genotype, and haplotype frequencies of *ADAM33* gene SNPs in Southwestern Iranian patients with asthma and healthy controls -------------------------------------------------------------------------------------------------------- **ADAM33** **Patients**\ **Controls**\ ***P*** **-value** **OR (CI95%)** **(n=150)** **(n=149)** -------------------------- --------------- --------------- -------------------- ------------------------ **Alleles** **T+1** **N (F%)** **N (F%)** G 221 (73.6%) 234 (78.5%) 0.19 0.7 (0.5 - 1.1) A 79 (26.4%) 64 (21.5%) **T1** G 82 (27.3%) 90 (30.2%) 0.49 0.8 (0.5 - 1.2) A 218 (72.7%) 208 (69.8%) **S1** G 248 (82.6%) 255 (85.6%) 0.39 0.8 (0.6 - 1.2) A 52 (17.4%) 43 (14.4%) **F+1** T 176 (58.6%) 172 (57.7%) 0.87 1.03 (0.75 - 1.4) C 124 (41.4%) 126 (42.3%) **Genotypes** **T+1** GG 77 (51.3%) 92 (61.7%) 0.1 0.6 (0.41 - 1.03) GA 67 (44.7%) 50 (33.6%) 1.5 (1 - 2.5) AA 6 (4%) 7 (4.7%) 0.8 (0.2 - 2.5) **T1** GG 6 (4%) 8 (5.4%) 0.69 0.7 (0.24 - 2.17) GA 70 (46.7%) 74 (49.7%) 0.8 (0.56 - 1.39) AA 74 (49.3%) 67 (44.9%) 1.1 (0.7 - 1.8) **S1** GG 99 (66%) 106 (71.1%) 0.41 0.7 (0.48 - 1.2) GA 50 (33.3%) 43 (28.9%) 1.2 (0.77 - 2.06) AA 1 (0.6%) \-\-- \-\-- **F+1** TT 28 (18.6%) 27 (18.1%) 0.7 1 (0.57 - 1.86) TC 120 (80%) 118 (79.2%) 1 (0.58 - 1.84) CC 2 (1.3%) 4 (2.7%) 0.4 (0.08 - 2.7) **Haplotypes T+1/T1/S1** **H1:** G A G 166 (55.33%) 181 (60.79%) 0.09 0.8008 (0.5784-1.1087) **H2:** A G G 77 (25.65%) 44 (14.75%) 0.00046 1.9933 (1.3205-3.0088) **H3:** G A A 50 (16.65%) 21 (7.11%) 0.00013 2.6381 (1.5411-4.5161) **H4:** G G G 5 (1.68%) 24 (8.12%) 0.0001 0.1935 (0.0728-0.5143) **H5:** A A A 2 (0.68%) \-\-- 0.25 \-\-- **H6:** A G A \-\-- 14 (4.82%) 0.000054 \-\-- **H7:** G G A \-\-- 8 (2.50%) 0.0037 \-\-- **H8:** A A G \-\-- 6 (1.90%) 0.015 \-\-- -------------------------------------------------------------------------------------------------------- ###### Deviation from Hardy-Weinberg equilibrium in the *ADAM33*gene in patients from southwestern Iran with asthma and healthy controls ---------------------------------------------------------------------------------------------------- **ADAm33**\ **Position** **Alleles** **HWE** **SNPs** ------------- -------------- ------------- --------- ------- ----------- ------- ------- ----------- **T+1** 3669480 G:A 0.447 0.388 0.1009 0.336 0.337 1.0000 **T1** 3669587 A:G 0.467 0.397 0.0509 0.497 0.422 0.0474 **S1** 3671118 G:A 0.333 0.287 0.0713 0.289 0.247 0.0574 **F+1** 3674438 T:C 0.8 0.485 \<0.00001 0.792 0.488 \<0.00001 ---------------------------------------------------------------------------------------------------- Obs HET: observed heterozygosity; Pred HET: predicted heterozygosity ![Linkage disequilibrium analysis of *ADAM33* gene SNPs in patients with asthma and healthy controls from southwestern Iran](IJBMS-21-813-g001){#F1} Although there are data showing a link between *ADAM33* and asthma, the exact role of this gene in the pathophysiology of asthma is not entirely clear ([@B5],[@B6],[@B15]). The contribution of *ADAM33* gene polymorphisms to the risk of asthma is controversial. Increased risk of asthma in persons with one or more *ADAM33*SNP allele(s) has been reported in African American, US white, US Hispanic, Dutch white ([@B16]), Icelandic, UK ([@B17]), and Japanese populations ([@B18]). We found no correlation between any of the four *ADAM33* SNPs (T1, T+1, S1, and F+1) and asthma in a sample of patients from the population of southwestern Iran. The lack of association between *ADAM33* polymorphisms and asthma was also reported in Australian ([@B19]), Chinese Li ([@B20]), Korean ([@B21]), Indian ([@B22]), and Turkish populations ([@B23]). In the only related report from Iran we are aware of, associations were found between the rs2280091 C allele and severe asthma, and between the rs2787094 G allele and moderate asthma in a population sample from northeastern Iran ([@B24]). Our results suggest that *ADAM33* gene polymorphisms play a restricted role in susceptibility to asthma. Although there is a possible linkage between undefined causal genes on the short arm of chromosome 20 and certain *ADAM33* SNP alleles or haplotypes, increased levels of *ADAM33* gene expression in response to environmental factors such as cigarette smoke or air pollutants might play a critical role in the induction of asthma. Moreover, the local formation of soluble ADAM33 in airways causes remodeling in the developing lungs, which through interaction with Th2-mediated inflammation makes patients more responsive to low concentrations of allergens ([@B25]). In this connection, there is evidence that in-utero and early-life tobacco smoke exposure influences the induction of TGF-β2, which in turn results in ADAM33 shedding and reduced lung function ([@B26]). However, in contrast to Reijmerink *et al*, who suggested a role for the interaction of cigarette smoke with certain ADAM33 polymorphisms in the induction of asthma ([@B26]), we found no association between the SNPs we studied and exposure to cigarette smoke in our patients with childhood or adulthood asthma. In contrast to Jongepier *et al*., who found an association between the S2 minor allele and decreased FEV~1~ ([@B27]), and in agreement with El-Falaki *et al* ([@B28]), we found no association between any of the four SNPs analyzed here and spirometry parameters. Previously, one study reported an inverse correlation between ADAM33 protein levels in bronchoalveolar lavage fluids and FEV~1~ in patients with asthma ([@B29]). However, we are not aware of any reports of a functional correlation between any *ADAM33* SNP alleles and ADAM33 protein levels in bronchial smooth muscle cells, bronchial lavage fluids, or serum in patients with asthma. Unlike Zhang *et al*., who reported associations between some *ADAM33* polymorphisms and concomitant allergic rhinitis and asthma in the Chinese Han population ([@B30]), and Matsusue *et al*, who found a link between rs2853209 and atopic dermatitis in Japanese children ([@B31]), we found no association between *ADAM33* SNPs and any spirometry indices. However, a potential limitation of our study is that we were unable to collect or process bronchoalveolar lavage fluid from our patients to analyze ADAM33 protein levels. Like another study, we also found a linkage between rs2280089 and rs2280091 loci ([@B32]). As shown in [Figure 1](#F1){ref-type="fig"}, this linkage was stronger in patients (*r*^2^ = 0.96) than controls (*r*^2^ = 0.87). Although we found no link between asthma and any of the *ADAM33* SNPs analyzed here, GGG haplotype was positively associated with the disease in our patients. This confirms the superiority of haplotype analysis over single-SNP analysis in studies that aim to elucidate the associations among different clinical, genetic, and environmental factors in complex genetic disorders such as asthma ([@B33]). Conclusion ========== We found no link between asthma and T+1, T1, S1, or F+1 SNPs in the *ADAM33* gene, however, AGG and GAA haplotypes of the first three SNPs were positively associated with the disease in our patients. *ADAM33* gene SNPs appear to play a partial role in asthma susceptibility, and investigation of expression changes in this gene in response to environmental factors or the local formation of soluble form of the molecule in the lung can be helpful to elucidate the impact of this molecule in the induction of asthma. The results presented in this paper were part of a student thesis for the MSc degree in Immunology (by Bent-Alhoda Hoseini-Pouya) and supported by a grant from Shiraz University of Medical Sciences, Shiraz, Iran (no: 7122). We thank K. Shashok (AuthorAID in the Eastern Mediterranean) for improving the use of English in the manuscript.
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Trichinella spp. in wild mesocarnivores in an endemic setting. Human trichinellosis and Trichinella infection in pigs are both still endemic in the Balkans, including Serbia. Because of the flow between the sylvatic and the domestic cycle of Trichinella spp., monitoring wildlife has been recommended for the risk assessment of Trichinella spp. infection in swine. We have previously shown the presence of Trichinella infection in wild carnivores including the wolf and the golden jackal, and here we report on Trichinella infection in several other mesocarnivore species. From a total of 469 animals collected between 1994 and 2013, Trichinella larvae were detected in 29 (6.2%, 95% CI = 4.0-8.4) animals, including 14 red foxes (4.7%), 7 wild cats (35%), 5 beech martens (4.8%), 2 pine martens (16.7%), and 1 European badger (6.25%). No Trichinella larvae were detected in the examined specimens of European polecats, steppe polecats and European otters. Species identification of the Trichinella larvae performed for 18 positive samples revealed T. spiralis in 77.8% and T. britovi in 22.2% of the isolates. Both species were detected in red foxes and wild cats. The predominance of T. spiralis in wildlife in Serbia indicates the (past or present) spillover of this pathogen from domestic to wild animals.
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Rocket Lab have unveiled a new, more economical propulsion system to get rockets into space. Auckland space technology company Rocket Lab has unveiled the world's first battery-powered rocket engine at the Space Symposium in the United States. The 3D-printed Rutherford engine, named after New Zealand-born physicist Ernest Rutherford, will power Rocket Lab's carbon-composite rocket, the Electron. Unveiled in 2014 but yet to be launched, the Electron is an 18-metre-long rocket designed to reduce the total time it takes to launch a satellite into orbit from years to just weeks. The rocket is expected to cost less than US$5 million (NZ$6.7m), making space more accessible. Supplied Rocket Lab chief executive Peter Beck says the Electron rocket's propulsion system is the first new rocket propulsion cycle created in 50 years. Rocket Lab founder and chief executive Peter Beck said the Rutherford engine is the world's first battery-powered rocket engine and the first new rocket propulsion system created in 50 years. "It will be pretty disruptive to the industry," Beck said. Unlike traditional propulsion cycles based on complicated and expensive gas generators, the Rutherford uses an entirely new electric propulsion cycle, using electric motors, batteries and software to drive its turbopumps. Supplied A test cell for Rocket Lab's Electric Rutherford engine - the world's first battery powered rocket engine. Turbopumps take propellant - in Electron's case a combination of liquid oxygen and jetfuel - out of the fuel tanks into the rocket engine to be burnt. The electric system made the engine much more efficient and cost effective, Beck said. The engine was produced using a 3-D printer which allowed Rocket Lab to make parts that could not be produced using alternative methods, he said. "That enables us to produce really high-performance components for these engines." 3D printers produced very robust, high-quality parts made from titanium and alloys and reduced manufacturing time from months to days increasing affordability, he said. The engine was unveiled at the Space Symposium in Colorado Springs, which has been running since 1984 and attracts more than 11,000 visitors. "It's the place to be," Beck said. The first launch of Electron was scheduled for the end of 2015 in New Zealand, Beck said. The Electron will be capable of sending payloads of 110 kilograms into orbit. Rocket Lab is a privately funded company. Its major investors include Khosla Ventures, Sir Stephen Tindall's K1W1 investment fund, Bessemer Venture Partners and Lockheed Martin, which designs and manufactures missiles and fighter jets for the US military. Rocket Lab has commitments for more than 30 launches and plans to carry out at least 100 launches per year.
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Many domestic appliances and electronic devices choose an external adapter to provide power. That is, an input plug of the external adapter is inserted into a power socket and an output plug of the external adapter is inserted into an interface of the electronic device to keep the electronic device working. However, the power socket is usually placed in a concealed location. Even if the electronic device is powered off or in standby mode, the electricity consumption still exists. Generally, the electronic device sets a switch adjacent with the interface of the electronic device to solve the problem of electricity consumption in standby mode. Turn off the switch to reduce the electricity consumption. However, the switch cannot cut off the input current of the adapter and the power of the adapter is nearly 0.5 W (watt).
3.109375
3
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Hello my name is Martina and today we're talking about the largest of all the planets Jupiter. Jupiter is the fifth planet out from the Sun and it's the largest out of all of the planets even if we can squish all the other planets together Jupiter would still be twice as massive. So, Jupiter is so big that it's 11 planet Earths wide or you would need around 1,300 Earths to build up Jupiter. Now Jupiter gets it's name from the Roman god who was the king of all of the gods the equivalent in other cultures are Zeus and Thor. A day on Jupiter and lasts just under 10 hours and a year on Jupiter the length of time to take one whole path around the Sun it's just under 12 years. Jupiter is the first of the gas giant planets we're gonna be looking at so it doesn't have any hard ground to land on it's atmosphere is mostly made up of helium and hydrogen much like a star. Now there's a reason that Jupiter didn't become a star even though it has a lot of the same elements as the star and the reason is it's just not big enough Jupiter would need to have had a mass seventy times that of what it does now before it could ignite nuclear fusion or essentially switch on as a star. So Jupiter just isn't big enough. Now Jupiter is the largest of all the planets it also has quite a lot of moons as well things as well in fact it has 79 moon that we know of so far. These moons are in orbit around the planet some of them are quite large, some of them are not very big at all. Jupiter's four largest moons called Io Europa Ganymede and Callisto and these can be seen through a small telescope in fact the first telescopes pointed to the night sky by Galileo in 1610 were able to see these four moons so Galileo's telescope was also able to see a Great Red Spot on Jupiter cloud tops this is a huge storm that has been raging on Jupiter for over 400 years so we can still see this storm today although it has shrunken and is becoming more circular in shape. Now when we think of rings around planets in the solar system Jupiter isn't often the planet that we think of but actually Jupiter does have its own ring system, in fact all the gas giants do, so we didn't know about Jupiter's ring system until the spacecraft Voyager flew past and took an image from behind Jupiter and we can see this dull ring system just there. So Jupiter is the fourth brightest object in the night sky after the Sun, the Moon and Venus So there's a good chance you've seen Jupiter. Now with the naked eye it does just look like a bright star like object and at the minute it's out in the very early hours of the morning. So I hope you enjoyed finding out more about Jupiter, join us next time were we will be talking all about Saturn.
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Mobile devices and other mobile equipment requiring power are used in many settings, including many where spare batteries in sufficient quantities to power the devices and equipment for a given task duration would be an intolerable burden and portable power sources are cumbersome and difficult to carry. One example is Army or Special Force military units operating in terrain where they cannot take a vehicle. A typical mission can last one to two weeks without re-supply. The weight and size of the required batteries for all of the unit's devices (e.g., radios, laser range-finders, computers, night-vision devices, enhanced optical sights, GPS receivers, etc.) for the complete duration of the mission is far more than is feasible to carry. Many other settings require power sources, such as search and rescue missions, geological and geographical survey teams, explorer teams, mountain climbing teams and other setting in which portable power sources are desirable. Portable generators have been available for a long time, but the portable generators and the fuel to operate the portable generators are often too heavy to be hand-carried for long distances.
3.078125
3
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Automatic speech recognition (ASR) systems try to determine a representative meaning (e.g., text) corresponding to speech inputs. FIG. 1 shows various hardware components of a typical ASR system such as a dictation system on a user desktop. A computer system 10 includes a speech input microphone 11 which is connected through a suitable preamplifier 13 to an analog-to-digital (A/D) converter 15. A front-end pre-processor 17 typically performs a Fourier transform so as to extract spectral features to characterize the input speech as a sequence of representative multi-dimensional vectors and performs the analysis and adaptation in a potentially derived feature space. A speech recognition processor 12, e.g., an Intel Core i7 processor or the like, is programmed to run one or more specialized computer software processes to determine a recognition output corresponding to the speech input. To that end, processor memory 120, e.g., random access memory (RAM) and/or read-only memory (ROM) stores the speech processing software routines, the speech recognition models and data for use by the speech recognition processor 12. The recognition output may be displayed, for example, as representative text on computer workstation display 14. Such a computer workstation would also typically include a keyboard 16 and a mouse 18 for user interaction with the system 10. Of course, many other typical arrangements are also familiar such as an ASR system implemented for a mobile device such as a cell phone, ASR for the passenger compartment of an automobile, client-server based ASR, etc. The ASR system compares the input utterances to find statistical acoustic models that best match the vector sequence characteristics and determines corresponding representative text associated with the acoustic models. More formally, given some input observations A, the probability that some string of words W were spoken is represented as P(W|A), where the ASR system attempts to determine the most likely word string: W ^ = arg ⁢ ⁢ max W ⁢ P ⁡ ( W ⁢ | ⁢ A ) Given a system of statistical acoustic models, this formula can be re-expressed as: W ^ = arg ⁢ ⁢ max W ⁢ P ⁡ ( W ) ⁢ P ⁡ ( A ⁢ | ⁢ W ) where P(A|W) corresponds to the acoustic models and P(W) represents the value of a statistical language model reflecting the probability of given word in the recognition vocabulary occurring. The acoustic models are typically probabilistic state sequence models such as hidden Markov models (HMMs) that model speech sounds using mixtures of probability distribution functions (Gaussians). Acoustic models often represent phonemes in specific contexts, referred to as PELs (Phonetic Elements), e.g. triphones or phonemes with known left and/or right contexts. State sequence models can be scaled up to represent words as connected sequences of acoustically modeled phonemes, and phrases or sentences as connected sequences of words. When the models are organized together as words, phrases, and sentences, additional language-related information is also typically incorporated into the models in the form of a statistical language model. The words or phrases associated with the best matching model structures are referred to as recognition candidates or hypotheses. A system may produce a single best recognition candidate—the recognition result—or multiple recognition hypotheses in various forms such as an N-best list, a recognition lattice, or a confusion network. Further details regarding continuous speech recognition are provided in U.S. Pat. No. 5,794,189, entitled “Continuous Speech Recognition,” and U.S. Pat. No. 6,167,377, entitled “Speech Recognition Language Models,” the contents of which are incorporated herein by reference. Many current speech recognition applications can benefit from long-term speaker adaptation using speaker logs, and for that, discriminative methods present a promising approach given its previous successes on acoustic model training. There have been large-vocabulary speech recognition experiments investigating feature-space and model space discriminative adaptation methods for long-term speaker adaptation. The experimental results suggest that though on average discriminative adaptation does not obtain a large gain over the ML-based baseline, there still are some test speakers that receive significant improvement. Speakers with high error rates under the speaker independent model tend to have larger gains with discriminative adaptation. These findings reveal that using discriminative methods for long-term speaker adaptation can provide advantages for speech recognition systems. But it is expensive to run adaptation for all speakers.
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Transducers generally convert electrical signals to mechanical signals or vibrations, and/or mechanical signals or vibrations to electrical signals. Acoustic transducers, in particular, convert electrical signals to acoustic waves and acoustic waves to electrical signals using inverse and direct piezoelectric effects. Acoustic transducers generally include acoustic resonators, such as thin film bulk acoustic resonators (FBARs), surface acoustic wave (SAW) resonators or bulk acoustic wave (BAW) resonators, and may be used in a wide variety of electronic applications, such as cellular telephones, personal digital assistants (PDAs), electronic gaming devices, laptop computers and other portable communications devices. For example, FBARs may be used for electrical filters and voltage transformers. An acoustic resonator can be formed by a layer of piezoelectric material between two conductive plates (electrodes), which can be formed on a thin membrane. Such a resonator can generate acoustic waves that propagate in lateral directions when stimulated by an applied time-varying electric field, as well as higher order harmonic mixing products. The laterally propagating modes and the higher order harmonic mixing products may have a deleterious impact on functionality. What is needed, therefore, is a structure useful in mitigating acoustic losses at the boundaries of the BAW resonator to improve mode confinement in the region of overlap of the top electrode, the piezoelectric layer, and the bottom electrode of a BAW resonator (commonly referred to as the active region).
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Q: Why is my output incorrect when in base 16 I am to write a program that lets me convert any number into any base. My program currently outputs "1669" for 366 base 16 when the correct output is 16E. Where is my code screwing up? #include <iostream> using namespace std; int main() { int iInter, iBase, iRemainder, i, iMax; int rgiTable[25]; char cAgain; do { do { cout << "Enter an integer greater than zero" << endl; cin >> iInter; cout << "Enter a base between the numbers 2 and 16" << endl; cin >> iBase; if (iInter < 0) cout << "Enter a new Integer" << endl; if (iBase < 2 || iBase > 16) cout<< "Enter a new base" << endl; } while (iInter < 0 || (iBase < 2 || iBase > 16)); for (i = 0; iInter > 0; i++) { iRemainder = iInter % iBase; iInter = iInter / iBase; if (iRemainder == 0) rgiTable[i] = 0; if (iRemainder == 1) rgiTable[i] = 1; if (iRemainder == 2) rgiTable[i] = 2; if (iRemainder == 3) rgiTable[i] = 3; if (iRemainder == 4) rgiTable[i] = 4; if (iRemainder == 5) rgiTable[i] = 5; if (iRemainder == 6) rgiTable[i] = 6; if (iRemainder == 7) rgiTable[i] = 7; if (iRemainder == 8) rgiTable[i] = 8; if (iRemainder == 9) rgiTable[i] = 9; if (iRemainder == 10) rgiTable[i] = 'A'; if (iRemainder == 11) rgiTable[i] = 'B'; if (iRemainder == 12) rgiTable[i] = 'C'; if (iRemainder == 13) rgiTable[i] = 'D'; if (iRemainder == 14) rgiTable[i] = 'E'; if (iRemainder == 15) rgiTable[i] = 'F'; iMax = i; } while (iMax >= 0) { cout << rgiTable[iMax]; iMax--; } cout << endl; cout << "Do you wish to enter more data? y/n" << endl; cin >> cAgain; } while (cAgain == 'y'|| cAgain == 'Y'); return 0; } A: When you print a digit using cout<< rgiTable[iMax]; you are printing an integer. When that integer value is equal to E, you get the ASCII value of E, which is 69. Instead of int rgiTable [25]; you should use char rgiTable [25]; In the while loop, use the characters '0' - '9' instead of numbers 0 - 9. You can simplify the logic using: for ( i=0; iInter > 0; i++) { iRemainder = iInter % iBase; iInter = iInter / iBase; if ( iRemainder < 10 ) { rgiTable [i] = iRemainder + '0'; } else { rgiTable [i] = iRemainder + 'A' - 10; } iMax = i; }
3.046875
3
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Ernest Mandel The Place of Marxism in History VIII. The reception and diffusion of Marxism throughout the world The explanation of the origins, content and development of Marxism must necessarily conclude with an analysis of its diffusion and real influence in the world. On the long run, ideas and overall bodies of ideas, that is doctrines, are worth what their impact on real history is worth. Ideas that never influence anything or anyone are necessarily marginal, even in the spiritual history of humanity, not to mention, of course, its material history. “Theory becomes a material force when it takes hold of the masses,” the young Marx had already said. The question of the time lag must of coarse be eliminated from this line of reasoning. Ideas that influence the world more and more some fifty or one hundred years after they were first formulated, are obviously more important than ideas that achieve an immediate impact but gradually decline thereafter, to the point of disappearing from the political scene. The decisive criterion is whether their social impact is reflected in material reality, sooner or later, on a broad, growing and – when dealing with the ideas that purport to strengthen the workers movement, socialism and the universal cause of human emancipation – on a world-wide scale, as befits the world-wide nature of the “social question,” the exploitation of the wage slaves, the oppression of the proletariat and all other oppressed human groups around the world: women, nationalities and oppressed races, etc. Finally, the particular characteristics of the proletariat, its position of economic and ideological subordination within bourgeois society, a subordination that is not overcome by its growing organisation, combatively and social weight, entail that the specific (and sometimes deformed) version in which Marxism is transmitted to the large working class organisations and popular masses at a given historical stage, leaves a definite imprint on the evolution of class consciousness. The latter combines with the former in a sense, positively or negatively depending on the circumstances. But this articulation cannot in turn be detached from the real march forward of the proletariat’s organisation and struggle, that is the real march forward of history. The reception and diffusion of Marxism throughout the world must therefore be examined on several successive levels: the narrow level of the diffusion of the writings of Marx and Engels; the level of the influence of its ideas outside the workers movement properly speaking, that is in intellectual and academic milieus, and more generally in “the spirit of the time” (the dominant ideologies of the successive phases through which bourgeois society has passed; inside the organised workers movement; inside the broad working class; at the international level. The circulation of the various writings of Marx and Engels was very uneven and marked by fits and starts. Some of their writings had a relatively rapid and broad impact, chief among them, the Communist Manifesto, which was translated into a large number of languages, and distributed in tens and then hundreds of thousands of copies (although even in this case, one had to wait for the 1920s and 1930s for its diffusion to become truly universal and be counted in the millions). Volume One of Capital also experienced a relatively rapid diffusion in a large number of languages, although on a smaller scale than the Communist Manifesto, usually a few thousand, not tens of thousands, copies in each language. The diffusion of almost all their other works, save for Engels’s Anti-Düring, was far more uneven and limited. In this regard, one should note that some of the major works of Marx and Engels were only published for the first time after a considerable delay, even in their original language, German. The Critique of the Gotha Program, Volumes Two and Three of Capital were only released in print twenty years after they were written; the German Ideology and the Grundrisse, some eighty years after they were written. This meant that three successive generations of Marxists did not have access to an adequate overall view of the doctrine of Marx and Engels, often only through sheer lack of information and data. We should note that some manuscripts of Marx still have not been published to this day. The last of his major economic works was only published in 1983. By the same token, works by popularisers of Marxism have generally had a far broader impact than the writings of the great masters themselves. In this respect, a special mention should go to the brochures of Karl Kautsky, above all The Economic Doctrine of Karl Marx and the Erfurt Program (of the SPD), hundreds of thousands of copies of which were printed in many languages. Other popularisation authors had a similar impact on a narrower scale, that is in one or a few languages. Among these were Bebel in German, Jules Guesde and Lafargue in French, Labriola in Italian, Iglesias in Spanish, Herman Gorter in Dutch, Plekhanov in Russian, De Leon and Debs in the United States. Their writings were far more widely read by the first generations of Socialists than the works of Marx and Engels themselves. The reception of Marxism in the academic and intellectual circles was even slower and more irregular. This should not surprise us. The reluctance of the bourgeoisie and upper layers of the petty-bourgeoisie to take Marxism seriously on the intellectual plane was commensurate with the intransigent opposition of Marx and the Marxists against not only the material interests of bourgeois society, but also against its most cherished “values.” The very fact that Marxist ideas were gaining greater influence among the masses was an additional argument for keeping them out of the educational system, the universities, the “official” textbooks. Save for a few rare exceptions – such as the Austrian economist Böhm-Bawerk, the Italian philosopher Benedetto Croce and the leader of the Czech bourgeoisie Thomas Masaryk – the appointed representatives of bourgeois ideology did not deign to polemicise against Marxism with a minimum of theoretical seriousness. This situation only changed towards the end of World War One, with the victory of the Russian revolution, the upsurge of the European labour movement from 1918 to 1923, the spread of communism in China and, a bit later, the economic crisis of the 1930s. Marxism progressively penetrated the academic world, first in Central Europe and China, India and Japan, then in the Anglo-American sphere. In France and Latin America, it only made a major breakthrough in intellectual milieus after World War Two. During the entire period of 1875 to 1900, polemics about Marxism were essentially confined to polemics inside the Socialist movement, under the stimulus of debates, attempted revisions and successive schisms, chief among which was the revision undertaken by one of Engels’s main intellectual collaborators and executors, Eduard Bernstein. All in all though, Marxism had a growing, albeit sometimes indirect, influence on the academic social sciences, mainly historiography and sociology, by introducing an increasing awareness of the importance of the “economic factor” and of social groups (as opposed to “great men”) in history. Thus, it refashioned the very concept of history, from a history of states and essentially political and military events, to a history of societies. Marxism’s impact on “official” economics was more belated. It affected mainly the field of the theory of economic fluctuations (business cycles), then that of large aggregates (macro-economic theory), especially from the 1930s, then the fields of planning and the analysis of imperialism and under-development, and finally that of the analysis of post-capitalist societies. The influence of Marxism inside the organised workers movement only developed in a decisive way with the creation of the large mass social-democratic parties in the years from 1885 to 1900 (in Germany: 1875 to 1900). It never achieved more than marginal influence in the mass trade unions of the Anglo-American cultural sphere. The same is basically true of the Labour Parties which emerged successively from these mass trade unions in Australia, Britain, New Zealand and most recently, English Canada. The social-democratic parties that eventually came together to create the Second International (through two rival congresses in Paris in 1889, a second united congress in Brussels in 1891, and a third, equally united, congress in Zurich in 1893) generally adopted the fundamental theses of Marxism in their programmes or professions of principle. Most were modelled on the Erfurt Program drafted by Kautsky with the close collaboration of Engels himself. Undeniably, this was a rather summary version of Marxism, boiled down to a few central ideas: the class struggle; the socialist goal of that struggle, through collective ownership of the major means of production and exchange; the conquest of political power to achieve that goal; international solidarity of the workers. But compared to the ideology of the first organisations of the working class, whether trade unions, co-operatives or political organisations, the doctrine that was thus popularised constituted a quite coherent whole that represented an enormous advance, especially since it was able to influence broad masses, contrary go the first communist sects and leagues. Its main weakness lay in its narrow determinism, verging on fatalism, that saw the supersession of capitalism by socialism in a more or less inevitable fashion, under the combined impact of economic evolution and Socialist organisation (of the workers), but failed to stress the political initiative and conscious action of the party. This often implied downplaying, even disparaging, direct mass action, not to mention revolutionary action and the destruction of the bourgeois state (“Generalstreik ist Generalunsinn”: general strike is general nonsense, the leaders of the German trade unions used to say.) Only after the Russian revolution of 1905 did a broad international current, embodied essentially by Rosa Luxemburg and the Russian Socialists Lenin and Trotsky, reclaim and revive the Marxist tradition of direct mass action and revolutionary initiative of the party. During the thirty previous years, that tradition had been marginalised inside social-democracy – except, partially, in Belgium – and confined to Anarcho-Syndicalist and Revolutionary Syndicalist circles (Spain, Britain, Argentina, partially the United States, Italy and France). Sometimes though, there was a more direct interaction between the organisational, electoral and trade-union expansion of international social-democracy in the quarter century that stretched from 1875 to 1900, and the actual spread of Marx’s ideas and works. A special case deserves mention in this respect: that of Finland. This small country under the boot of Tsarism succeeded in the span of one decade, between 1899 and 1911 in creating one of the most powerful and combative workers movements of the world. The rapid ascent of this party was to lead in 1917-1918 to the deepest and most tenacious proletarian (but also most repressed) revolution outside Russia. In the parliamentary elections of 1913, the Finnish Socialists obtained 43% of the vote, the highest figure in Europe, more than the German social-democracy. They then extracted from the Diet a decision to publish Volume One of Marx’s Capital, at Parliament’s expense! The penetration of Marxist ideas and doctrine among the broad working masses during the epoch of the Second International has generally been exaggerated by historians, including those of the labour movement. In fact, the masses of workers formed their political and trade union beliefs through the filter of two experiences: their day-to-day struggles for immediate demands (economic goals and universal suffrage, in a few countries national-democratic demands were added to this set); and the regular education dispensed by the Socialist press and Socialist rallies. There already was a big gap between Marxism as a coherent doctrine and the summary Marxism of social-democratic programmes. From these programmes to the practice, to the day-to-day experience and education of the workers, the distance was even greater. Systematic political education of workers was conducted on an extremely small scale. Marxist theoretical reviews, including the most prestigious, the Neue Zeit, only succeeded in reaching a few thousand subscribers (10,000 in the case of the Neue Zeit). The central schools of the parties, including that of the SPD, which had one million members, did not bring together more students than the present school of the Fourth International. This limited penetration of Marxism among the masses can be illustrated by an example. In Milan, the fortress of Italian socialism, public libraries loaned 264,000 books in 1910. Forty-four percent of the loans were to workers, and 32% to students. The names of Marx and Engels do not appear once among the authors of books loaned out! What Marxism brought to the masses, beyond strong political organisations and the general understanding of the need to combine trade union action with class independence and political action – including international action – was a general feeling of marching “with history”: the feeling that capitalism was doomed and that socialism must succeed it. About the manner in which the transition from the former to the latter would take place, there were few precise ideas and even little substantive debate. Serious discussion was basically confined to the spheres of the most active political activists, and even to the upper spheres of the party. It concerned thousands of individuals whereas the Socialist movement numbered in millions. It only penetrated deeper into the masses towards the end of the 1914-1918 world war, that is when it was posed in practice under the combined impact of the war and the great proletarian revolutions that emerged from it: the Russian, Finnish, German, Austrian, Hungarian revolutions, as well as the revolutionary crisis in Italy. Nevertheless, Marxist doctrine had a deep effect on the masses, sometimes through indirect and unforeseen mediations that should not be underestimated. An example of this sort of progression is the struggle for the shortening of the working day to eight hours. Marx was the great propagandist and the great educator of the international workers movement on the emancipatory value and importance of the shortening of the workday. The idea of an international action by male and female workers for a class goal common to the proletarians of all countries, is also clearly an idea of Marxist origin. But in practice, the decision to turn May Day in all countries into an international day of strike for the eight-hour day, only became widely accepted after five Anarchist leaders in Chicago, the Haymarket martyrs, were accused of having thrown a bomb at the police, condemned to death and executed in 1886. This tragedy was needed to inflame the imagination and sensitivity of the workers on a mass scale. It was the event which triggered a powerful, and, in the long run irresistible movement (the eight-hour day was eventually won in almost all industrialised countries); the spark of Marxist thought and propaganda alone proved inadequate for that job. A certain confusion developed among the masses around the end of the 19th century, as the revolutionary content of Marx’s and Engels’s doctrine was undermined from within social-democracy by Bernstein’s revisionism and the ministerial collaboration advocated and then practised by Millerand in France and Bissolati in Italy. The confusion was particularly grave because this revisionism, although rejected on the plane of ideas by most well-known social-democratic leaders identified with Marxism, actually increasingly corresponded to their day-to-day practice. This was particularly true of Anseele and Vandervelde in Belgium, Troelstra in the Netherlands, Branting in Sweden, Stauning in Denmark, Greulich in Switzerland, Palacios and Justo in Argentina, and, to a large extent, Victor Adler in Austria. Only Bebel in Germany, Guesde in France, and Sen Katayama in Japan, were intransigently consistent in their opposition to the revisionist practice and theory spreading during this period. But Bebel’s and Guesde’s intransigence crumbled in the years that followed the Russian revolution of 1905, around 1910. (Guesde became a minister in the so-called “Sacred Union” bourgeois coalition government of 1914). Only Katayama remained an intransigent Marxist. While it is true that Marxist theory was not widely disseminated among the masses in its original and integral version, another myth also needs to be refuted, namely the claim that even the few key ideas of Marxism incorporated into their programme and propagated by the first mass social-democratic parties, did not really influence the consciousness of the masses. This claim is particularly wrong with respect to internationalism. There were in fact impressive practical demonstrations of proletarian internationalism in the heyday of the Second International. It was precisely because that practice had existed that the betrayal of August 1914 appeared so disorienting to the broad masses, and monstrous to the Socialist left. Shortly after the outbreak of war between Russia and Japan in 1904, the Socialist leaders of these two countries, Plekhanov and Sen Katayama embraced at the Congress of the International in Amsterdam, and proclaimed their shared opposition to the war and to the ruling classes of their respective countries who had provoked it. When the Russian revolution of 1905 broke out, it elicited a powerful movement of international solidarity. In fact, it triggered a radicalisation of the workers struggles in several countries, notably a general strike for universal suffrage in Austria. When the Swedish bourgeoisie tried to stop the movement for Norwegian independence by a military intervention in 1906, the congress of the Swedish social-democratic party decided to oppose the war by all means, including a general strike, and organised a gigantic demonstration in Stockholm that forced the government to back off. In 1913, the Italian Socialist Party despite a chauvinistic campaign supported by one third of its own parliamentary caucus, organised a general strike against Italy’s colonialist expedition to Tripoli (Libya). At that point, Marxist education, the deepening and enrichment of Marxism, its application to the new analytic and strategic problems posed by the onset of the era of imperialism, were pursued mainly by the Socialist left. This left developed mainly inside the Social- Democratic Parties themselves until 1914 (1917 and even 1920), although in several countries it led to splits even before World War One: Russia, Poland, the Netherlands, Bulgaria. Elsewhere, Revolutionary Syndicalist currents developed certain aspects of Marxism outside the Socialist Parties. This Marxist left was to lead up to the creation of the Third International following the great revolutions of 1917 to 1919. The most striking phenomenon of this entire period of growth of mass political parties influenced by Marxism, was the world-wide extension of its influence, touching successively Western and Central Europe, then the United States, Southern and Eastern Europe (Russia, the Balkans), Asia (Armenia, Georgia, Iran. Japan, China, India, Indonesia), Latin America (Argentina, Uruguay, Brazil, Mexico, Cuba, Chile), Australasia (Australia, New Zealand) and Africa (Egypt, Tunisia, South Africa). By rebound, but with some delay, the specific problematic of the colonial and semi-colonial countries was progressively integrated into Marxist analysis and practice, particularly after the Russian, Iranian and Chinese revolutions of 1905 to 1912. It should be noted that this process basically did not take hold during the Mexican revolution of 1910 to 1917, the last great contemporary revolution in which no clearly Marxist current emerged. At the end of the third congress of the Socialist International held in Zurich, on August 12, 1893, Friedrich Engels, who was seated in the hall as a simple delegate, was carried to the podium by an immense ovation. Moved by the gesture, the old militant regretted that Karl Marx, his companion of so many struggles, had not witnessed this upsurge of the organised labour movement world-wide. He then expressed his unshakeable confidence in “the new, stronger, invincible international.” Glancing back over the fifty-two years of his political life, looking at the cities of Vienna, Berlin, Paris and London, he proclaimed that “Marx and himself had not struggled in vain, that they could look back on their work with pride and satisfaction.” He concluded: “There is not a single country, not a single great state where social-democracy is not now a power that all must heed. We are, we too, ‘a great power’ that is feared. The future depends far more on it and on us, than on any one of the bourgeois ‘great powers’!”
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A replication technique for replicating data is known as a measure to protect against data loss. Among processes that use the replication technique are backup and disaster recovery (DR). A storage area in which data on an application is stored is called a data volume. Backup refers to the process of storing data in the data volume at a given point in time and storing it for a long period of time. DR refers to the process of constantly replicating data in the data volume so that the replicated data can be used in other systems. Examples of replication include host-based replication performed on a host computer and array-based replication performed on a storage system. In the host-based replication, Write data (data to be written) to be written to a data volume from an application is captured to create a replica volume that has stored therein the same data as the data volume. As the Write data from the application is written to a medium by transfer, the host-based replication can accommodate a heterogeneous environment without dependence on the storage devices. Further, the replica volume can be created at low cost. In the array-based replication, a replica volume is created using a replication function of the storage. This allows creation of a replica volume that maintains the consistency among of a plurality of hosts without imposing load on the hosts. As disclosed in Patent Document 1, there is known an environment that supports both host-based replication and storage-based replication. When such an environment is used, it is possible to effectively use their respective advantages. For example, when attempting to acquire backup data that maintains the consistency among a plurality of hosts, the administrator performs a backup operation using local-array-based replication. Meanwhile, when attempting to perform DR operation at low cost by utilizing the existing resources, the administrator would consider DR operation using host-based replication. As described above, an administrator who desires to perform an operation using both host-based replication and array-based replication is envisaged. Patent Document 1: JP Patent Publication No. 2005-062928
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Big Idea: Changing shoes is connected to a character analysis. Why do we change shoes? The Common Core Standard is RL.1.3, which states that students should be able to analyze how and why individuals, events, and ideas develop and interact over the course of a text. I try to provide an opportunity for students to develop this skill by introducing it with a real life connection. I also allow my students to read a variety of high quality literacy texts over a broad range of subjects to meet the college and career readiness goals. Lesson Overview In this lesson students listen to me explain why I change clothes. Learners are given a choice of texts to use to analyze the character. The texts are pre-selected based on their lexile level. I feel that 1st grade students need to be reading at their current lexile to improve fluency (though I supplement with read alouds that are complex also so that students can be exposed to richer texts). Introductory Activity I seat the class on the lounge next to their collaborative partner. I ask them to discuss why they might change shoes or clothes. After about one minute, I tell them that one time I fell in a mud hole at school and my Mom had to bring me clothes. Then I explain that today we are going to analyze why character do the things they do in a text. I chose to connect character analysis to changing shoes because it is something that everyone does. This allows them to connect themselves personally to what I am talking about. It creates engagement. The students can identify with the person changing their shoes and this personal connection helps students understand and analyze the character. In the guided practice the story of my bad day is great because everyone has had a bad day. So, my students can connect to the story. This personal connection allows the students to more easily analyze the character. As I begin the guided practice, I tell them the story about my terrible day. It was awful. First my son's babysitter was sick; then my instructional coach came by, and I did not capitalize Nintendo when I was writing; and last I forgot my lunch. I show the class the Model I made (you can find it in the resource section). It is a big piece of bulletin board paper and cut into two sections. To help the students organize their thoughts I use a simple graphic organizer. The top tells about the day and the bottom tells why. I like to add illustrations to help show meaning, and I added them to the best of my ability. Then I explain these are the reasons that I had a bad day. I then tell the students I want them to tell me about their bad day. I allow the students to tell their partner what happened first in their bad day. Common Core really supports collaboration. I then ask how this made the day bad. I listen and share what I heard. Then they discuss what happened in the middle of their bad day. I ask them to discuss why this made the day bad. I share what I heard on group say. The students then share the ending of their bad day. Last, I ask one student to tell me about their bad day from the beginning to the end. I write the information on the graphic organizer. As I wind up this section, I ask why and how each detail made the day bad and add that to the graphic organizer. If the student had any interaction with others over the course of the bad day I ask them to explain the connection between that person and the day. I am trying to give my class a personal and real application for how and why characters interact. Resources (2) Resources I try to give my students choices often so I allow them to choose a text and analyze the characters. In order to try to engage my students I provide texts that I think my students are familiar with and are lexiled at their level. Since the students worked with me in the guided practice I feel that they are ready to try to organize their own thoughts on their own graphic organizer. I try to provide the example for everyone so I hang my model up for them to reference. Sometimes students go up the seats closer to the model when they need help. I really want to encourage Collaboration so my students are working in heterogeneous groups of two or three and seated at the center tables. I select the groups based on ability, personality, and gender. I want to show my students I respect their feelings and I try to keep them comfortable in their grouping. I want to create the best learning environment I can. There is a great video (Student Work) of their work in the resources. You can check it out if you like. Resources (2) Resources At the end of the lesson, I have students meet me in the lounge area to share out what they noticed about characters in their books. I find that this gives students some time to practice speaking and listening skills, but I make sure to go over the rules of speaking and listening extensively before having students share out. It’s better to be proactive than to correct misbehavior, right? After we listen to about two or three volunteers, I ask students to draw a conclusion about what we learned today. First students discuss their ideas with their partner, which engages everyone and gives them a chance to practice before sharing to the whole group. Then, when I call on students, they feel more comfortable because they had the chance to practice. For this particular share out, I make sure to listen closely for students to explain that they learned about analyzing characters’ interactions.
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Q: Why does the expansion of gas into a vacuum mean that we have less information about the system? (entropy) I'm reading through Statistical Physics by F. Mandl and in the chapter about the 2nd law of thermodynamics he states that: The basic distinction between the initial and final states in such an irreversible process is that in the final state we have a less complete knowledge of the state of the system. Why is this true? Let's say our gas exists in the left side of a container separated by a partition. We know that all the molecules are definitely on the left side. Now we remove the partition. The gas rushes into the vacuum and eventually spreads itself throughout the container. The book mentions that macroscopic fluctuations of the gas moving around would not be observable unless we waited for a period of time around the order of the age of the universe. So then if we assume that 50% of the gas is on the left side and 50% is on the right side (assume that the partition is infinitesimally thin and unbreakable/unbendable), then how is it that we know less information of the system in this state? A: Partially answered already in the question and comments. CuriousOne answered it. Entropy is a measure of the possible microstates of the system, i.e., the different positions and velocities of each of the molecules. When you double the volume each of the molecules doubles the number of possible x, y, and z's. The possible number of states has increased. S has gone up.
3.140625
3
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Q: Question about standing wave By considering the superposition of two waves propagating through a string, one representing the original or incident wave and the other representing the wave reflected at the fixed end, if both ends of the string is fixed then the waves can reflected and travel back and forth. Standing wave can be formed if the length of the string is an integer numbers of half wavelength. I just wonder what will we get if the length of the string is NOT an integer numbers of half wavelength and both ends are fixed? A: According to "Fundamentals of Physics 9ed" by Halliday Resnick (p. 496), "there will not be a steady wave pattern with nodes and antinodes, and the total wave will not be a standing wave." The result will be somewhat like waves reflecting off the irregular shores of a tiny pond - unrecognizable patterns, or like confused seas on the ocean, where the waves generated by several different weather patterns meet. This kind of confusion is notoriously difficult for a sailboat to navigate, because the patterns change frequently and unexpectedly.
3.65625
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B OSNIA-HERCEGOVINA might have a new government soon. Or maybe it won’t. No one seems to know. The country held elections last October but the winning parties have still not agreed on how to form one. In any case, Bosnia’s central government has little power; the country has three presidents, and their current chairman wishes it did not even exist. Tens of thousands of people emigrate every year, having lost any hope for the future. From 1992 to 1995 Bosnia was the Syria of its day. Some 100,000 people died in the three-way war between the country’s communities: its Orthodox Serbs, its Catholic Croats and its Muslims (often referred to as Bosniaks). Unlike in Syria, though, Western powers intervened and eventually ended the shooting. A peace agreement was signed at an American airbase in Dayton, Ohio, and 60,000 peacekeepers were sent to make it stick. But today few believe that the complex deal made to end the war now delivers good governance. And there is no political will to reform the country in a way that could benefit everyone. Bosnia’s central government has few powers, but co-operation with NATO is one of them, and disagreements about this are an obstacle to forming a new administration. Most power lies further down. Under the Dayton accords, the country was divided into two statelets. One is the Republika Srpska, populated overwhelmingly by Serbs, which is itself split into two pieces because a region around the town of Brcko was allowed to be autonomous. The other is a Bosniak-Croat federation, consisting of ten cantons. Many Croats want this federation to be divvied up, too, because they argue that the Muslim Bosniaks, who are more numerous, can always outvote them. The war swept away a tolerant and mixed society, yet Bosnians still work, trade and sometimes drink coffee together. They do not tend to live together, though, and mostly vote for nationalist parties which in turn parcel out jobs and patronage.
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Respiratory Asthma Triggers Lurk Indoors in Winter People who have seasonal allergies often view winter as a time of year to catch a break. The lack of airborne pollens and grasses has many of them breathing a sigh of relief. But for some people with asthma, the wind and cold are just backdrops to a season of misery. This is because they are sensitive to indoor allergens. Spending more time inside brings greater exposure to dust, pet dander, mold, cockroaches, and other allergens. Asthma triggers cause airways to swell and narrow, making it hard to breathe. But you can help prevent allergy-induced asthma symptoms in the home. What you can do Control dust mites Dust mites are tiny bugs that live in dust. They are mostly found in mattresses, pillows, carpet, and bedding. Their droppings are a common allergy and asthma trigger. Be sure to: -Cover mattresses and pillows with airtight covers. -Keep household humidity below 40 percent. -Remove carpets, rugs, and heavy curtains from bedrooms. -Wash bedding in hot water every 7 to 10 days; dry in a hot dryer. -Remove extra clutter that will collect dust. -Dust weekly with a damp cloth. Wear a respirator when you dust. -Vacuum rugs and carpets at least once a week. Eliminate mold Molds are microscopic fungi with spores that float in the air. Mold grows in moist places during the winter or areas that may not be routinely cleaned and disinfected:
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The primary challenge of rocket propulsion is the burden of needing to accelerate the spacecraft's own fuel, resulting in only a logarithmic gain in maximum speed as propellant is added to the spacecraft. Light sails offer an attractive alternative in which fuel is not carried by the spacecraft, with acceleration being provided by an external source of light. By artificially illuminating the spacecraft with beamed radiation, speeds are only limited by the area of the sail, heat resistance of its material, and power use of the accelerating apparatus. In this paper, we show that leakage from a light sail propulsion apparatus in operation around a solar system analogue would be detectable. To demonstrate this, we model the launch and arrival of a microwave beam-driven light sail constructed for transit between planets in orbit around a single star, and find an optimal beam frequency on the order of tens of GHz. Leakage from these beams yields transients with flux densities of 0.1 Jy and durations of seconds at 100 pc. Because most travel within a planetary system would be conducted between the habitable worlds within that system, multiply-transiting exoplanetary systems offer the greatest chance of detection, especially when the planets are in projected conjunction as viewed from Earth. If interplanetary travel via beam-driven light sails is commonly employed in our galaxy, this activity could be revealed by radio follow-up of nearby transiting exoplanetary systems. The expected signal properties define a new strategy in the search for extraterrestrial intelligence (SETI). James Guillochon (1), Abraham Loeb (1) ((1) Harvard ITC) (Submitted on 12 Aug 2015) Comments: 6 pages, 5 figures. Submitted to ApJL Subjects: Instrumentation and Methods for Astrophysics (astro-ph.IM); Space Physics (physics.space-ph) Cite as: arXiv:1508.03043 [astro-ph.IM] (or arXiv:1508.03043v1 [astro-ph.IM] for this version) Submission history From: James Guillochon [v1] Wed, 12 Aug 2015 20:05:20 GMT (1463kb,D) http://arxiv.org/abs/1508.03043 Please follow Astrobiology on Twitter.
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Per cent mille A per cent mille or pcm is one one-thousandth of a percent. It can be thought of as a "milli-percent". It is commonly used in nuclear reactor engineering as a unit of reactivity. Reactivity In nuclear reactor engineering, a per cent mille is equal to one-thousandth of a percent of the reactivity, denoted by Greek lowercase letter rho. Reactivity is a dimensionless unit representing a departure from criticality, calculated by: where keff denotes the effective multiplication factor for the reaction. Therefore, one pcm is equal to: This unit is commonly used in the operation of light-water reactor sites because reactivity values tend to be small, so measuring in pcm allows reactivity to be expressed using whole numbers. See also InHour (another unit of reactivity) Dollar (reactivity) Notes Category:Units of measurement
3.25
3
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Lubrication involves the process of friction reduction, accomplished by maintaining a film of a lubricant between surfaces which are moving with respect to each other. The lubricant prevents contact of the moving surfaces, thus greatly lowering the coefficient of friction. In addition to this function, the lubricant also can be called upon to perform heat removal, containment of contaminants, and other important functions. Additives have been developed to establish or enhance various properties of lubricants. Various additives which are used include viscosity improvers, detergents, dispersants, antioxidants, extreme pressure additives, and corrosion inhibitors. Fuel efficiency is one of the most challenging areas in today's lubricant development. Friction modifiers are widely used in lubricant formulations. Organic molybdenum compounds are very effective friction modifiers. However, corrosion is one of the main factors that limit the broad use of high concentrations of organic molybdenum compounds. There are two commonly used organic molybdenum compound friction modifiers, namely molybdenum dialkyldithiocarbamate (MoDTC) and molybdenum dialkyldithiophosphate (MoDTP). It is also known that these molybdenum compounds contribute to copper corrosion. See, for example, EP 0316610A1 and R. T. Vanderbilt literatures that indicate in some formulations, the presence of Molyvan™ 822 (MoDTC) and Molyvan™ L (MoDTP) contribute to copper corrosion which is detrimental to some diesel engines. The corrosion issue is one of the key factors that limit the use of high concentration of organic molybdenum compounds in formulating high fuel economy lubricants. Despite advances in lubricant oil formulation technology, there exists a need for an engine oil lubricant that effectively improves corrosion protection and friction coefficient in order to improve engine durability and fuel efficiency.
3.15625
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In computers or arithmetic hardware, integer and floating-point formats have been widely used to simply describe values that are extremely-large or extremely-small. In the integer format, it is easy to make the hardware to carry out calculations, however, there is a drawback in that the integer format can represent a small range. Thus the algorithm must be scaled such that overflow does not happen. In the floating-point format, a wide range of values can be represented and the algorithm does not need to be scaled to prevent overflow. IEEE-754 format is the most commonly used for floating-point representation. FIG. 1 shows an example of a conventional floating-point format. The floating-point format is constituted by a 1-bit Sign, a 7-bit Exponent and an 8-bit Mantissa. The addition of values in the floating-point format is complicated, and the circuit size and the logic delay are large. However, so far, since there is no numerical format by which the floating-point format can be replaced, a lot of researches have been made for the calculation in this format. FIG. 2 illustrates a floating-point adder of a conventional style. First, absolute values of two inputs X and Y are compared in swapping unit 201. The larger one is selected as A and the smaller one is selected as B. Here E(x) represents the exponent and M(x) represents the mantissa for floating-point number x. If X>Y, E(X) and M(X) are respectively output as E(A) and M(A). In a barrel shifter A 203, the mantissa for B (M(B)) is shifted to the right direction based on the difference between E(A) and E(B) calculated by subtracter 202. This is referred to as an alignment. Then in a fixed point main adder 204, the mantissa for A (M(A)) is added or subtracted with the shifted M(B) according to the sign bit of X and Y. The calculation result from the fixed point main adder 204 is provided to a leading zero counter 205, which counts the number of consecutive zeros from the most significant bit (MSB) and outputs the leading zero count to a barrel shifter B 206. The leading zero count is also used to adjust the exponent. When the subtraction happens and the result becomes smaller, the calculation result of the fixed point adder 204 is shifted left depending on the leading zero count by a barrel shifter B 206, which is referred to as a Normalization. The barrel shifter B 206 outputs the shift result to a rounding unit 208. The subtracter 207 subtracts the leading zero count from the exponent E(A) and outputs the subtraction result to the rounding unit 208. The rounding unit 208 executes rounding and outputs E(Z) and M(Z) as the final calculation result. In FIG. 2, the dotted line shows a critical path in the floating-point adder. The value of a floating-point number X in the conventional floating-point format is expressed using the integer values of exponent E(X), mantissa M(X) and sign S(X) as a following formula (1).X=(−1)S(X)(M(X)+h)2E(X)+q  (1) Herein q is an integer constant for the offset, and h is an integer constant representing the hidden mantissa. Even with the type of floating-point adder shown above, its implementation is complicated and the size of the adder is several times larger than the integer adder because the barrel shifter and the subtracter need relatively large size logic circuits, which make the critical path longer. In addition, a logic delay of the adder is also large, which results in the operating clock frequency being limited and is sometimes required to prepare additional pipeline stages that also require the extra hardware size.
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In light of the recent theft from a Norway museum of Edvard Munch’s 1893 painting, The Scream, we posed these questions to professors in the Art Department: What is the significance of The Scream from an art historical perspective? What is the value of classic artwork in today’s society? Dr. Sarah Glover assistant professor of art Munch’s use of vibrant color, expressive line, and distorted form transformed the act of seeing into one of feeling. Freed from the traditional boundaries of narrative, The Scream’s full force arises, not simply from the subjects in the painting, but from the vicious tonalities and sweeping lines that define the tortured figure in the foreground as they simultaneously envelop and suffocate him. The intense emotional content of Munch’s work, and the visually direct way this content is communicated, paved the way for the Expressionist painters of the early 20th century. The work also solidified the trend in interpreting painting as autobiographical. The cathartic qualities of Munch’s work seem to offer a glimpse into the mind of the artist. This aspect of his work is often used to support the rather tired, but seemingly much loved, notion of artists as outsiders, as tormented individuals. Although The Scream was, for Munch, intensely personal, the anxiety and anguish it conveys is universal. It is the painting’s accessibility, its universal qualities, that makes it a “classic” work. This status is proclaimed in the image’s proliferation. Munch himself made many versions of The Scream, in paint and print. Andy Warhol replicated the image countless times in an attempt to both comment upon, and deflate, its visual impact. The reproductions of Munch’s image have increased in recent decades. The painting’s open-mouthed figure now gapes at us from coffee mugs and t-shirts. The anguished form is sold as an inflatable doll, an object which, the buyer is assured, will make “a great addition to any college dorm room.” It would be easy to condemn this treatment of Munch’s image, but, in many ways, the commercialization of The Scream is a testament to its iconic power. Although the kitschy versions of Munch’s image are more comical than horrifying, they demonstrate an attempt to distance ourselves, through laughter, from the painting’s brutally direct critique of humankind’s failings. Like most masterpieces, The Scream’s imagery continues to have meaning, despite being removed from its original visual and historical context. Today the image is still effective as it can serve, not merely as a window into Munch’s thoughts, but as a reflection of our own culture of fear. Professor Harold Linton chair, department of art So much has already been written on Edvard Munch and the recent theft of one of his works from a Norwegian collection. Classic works of art and design such as The Scream by Munch possess many lessons for society and those who take the time to observe great art. Art is created from judgment and not strictly rules. It teaches us about forming opinions and making qualitative relationships and therefore about understanding our own feelings and becoming aware that there are more than one set of solutions to a problem and more than one answer to a question. Munch created several interpretations of this scene in the form of paintings, drawings, and printmaking. Each of these variant compositions reflect research into his own feelings and his reactions to landscape-horizon transformed by a fiery red light of vast proportion that he experienced on this day. The most famous version of The Scream was painted in 1893 as part of The Frieze of Life, a group of works derived by Munch’s personal experiences, including the deaths of his mother in 1868 and his sister in 1877. These works were created in the 1890s, but have established origins in earlier decades. For those who have ever wondered why the sky was a lurid red in The Scream – Edvard Munch’s painting of modern angst – astronomers have an answer. They blame it on a volcanic eruption halfway around the world. An analysis of the phenomenon that contributed to the creation of the painting was first published in Sky and Telescope journal. The article pinpointed the location in Norway where Munch and his friends were walking when the artist saw the blood-red sky depicted in the 1893 painting and offered the following explanation for why the sky seemed to be aflame. Astronomers determined that debris thrown into the atmosphere by the great eruption at the island of Krakatoa, in modern Indonesia, created vivid red twilights in Europe from November 1883 through February 1884. The phenomenon was widely seen and reported in local newspapers. Astronomers suggest that Munch drew his inspiration for the sky in the painting from these volcanic twilights, and not strictly from his own imagination. What better source for inspiration, however, than that of extraordinary events by Mother Nature. The dramatic phenomenon of such great magnitude that followed the eruption was experienced for months around the world. Five recognized at convocation Five Bradley faculty and staff members were recognized for their achievements in teaching, scholarship, and service during the annual Founder’s Day Convocation. Dr. Allen Huffcutt, professor of psychology, recipient of the Samuel Rothberg Professional Excellence Award; Virnette House-Browning, senior associate athletic director/senior woman administrator, recipient of the Mergen Memorial Award for Public Service; Dr. John Jost, professor of music and director of choral activities, recipient of the Putnam Award for Excellence in Teaching; Dr. Sarah Glover, assistant professor of art, recipient of the Caterpillar Inc. Faculty Award for Teaching, and Dr. William Wilcox, assistant professor of accounting, recipient of the Caterpillar Inc. Faculty Award for Scholarship. You‘re Hired The Smith Career Center hosted a successful fall job fair on September 23. A record-breaking 1,100 students attended the fair that showcased 139 employers who offered face-to-face discussions about co-ops, internships, and full-time job opportunities.
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A laser can be used to machine a work piece by removing material or by drilling through the work piece. The laser can provide an unfocused laser beam that has a generally circular transverse cross-section relative to a beam axis A-A with spot size and power (or “irradiance”). The spot size is typically defined as the radial distance from the center of maximum irradiance to a location proximate 0.135 or 1/e2 times the maximum irradiance of the laser beam and measurable with a suitable device. Other techniques can also be used, alone or in conjunction with the previous technique to define the spot size such as, for example, a second moment technique. The spot size can be focused by an optical assembly to a smaller spot size (i.e., a focusing spot size) so that the power of the laser beam can be concentrated over a smaller area, thereby allowing the laser beam to deliver a sufficient power density to the work piece in order to laser machine the work piece. In laser machining the work piece, the power being applied to the work piece needs to be an appropriate magnitude so that the focusing spot can liquefy, vaporize, and/or ablate the material of the work piece. Where the power being delivered to the focusing spot is much greater than is needed, the focusing spot may cause the work piece to form a heat affected zone (thereby distorting the work piece) or splatter/recasts (thereby affecting the surface finish). To control the power being delivered to the focusing spot, pulse repetition rate, pulse width, and the laser itself, might be changed. It is commonly believed that a shutter like iris is interposed between the laser beam and the optical focusing assembly. The iris operates to reduce the area of laser light passing through the iris, thereby controlling the power of the focusing spot. The size of the focusing spot in this set up is generally inversely related to the size of the opening of the iris. As such, whenever the power of the focusing spot size is controlled by changing the beam diameter of laser light passing through the iris, the focusing spot size changes in an inverse manner. For example, when the unfocused beam diameter is reduced through the iris, the focusing spot size increases. The increases in focusing spot size can therefore change the resolution at which the focusing spot size can machine the work piece. Furthermore, when the focusing spot size is changed, the depth of focus of the focused beam changes, which could require the work piece to be repositioned so that the work piece is within this depth of focus for consistent laser machining results. In order to maintain the same focusing spot size or depth of focus, it is believed that the focal length of the focusing lens could be changed to a shorter focal length lens. However, changing the focusing lens could require additional set up time that would affect the overall production efficiency of the laser machining process. Furthermore, when the focal length is reduced, lens aberrations tend to increase. Even though lens aberrations may be correctable using multiple-element focusing optics that would, again, add to set up time and potentially the ability to manufacture the work piece efficiently. Thus, there is an interplay between at least the beam diameter, focusing spot size, focal length of a focusing lens, focusing depth, and even the type of material or dimensions of the work piece that must be taken into consideration whenever the laser power is controlled to a magnitude below its maximum power. This interplay is believed to increase the complexity of the laser machining system. It would be desirable to maintain a constant focusing spot size regardless of the beam diameter or power being delivered to the focusing spot. It would also be desirable to maintain a generally constant depth of focus regardless of the power being delivered to the focusing spot. It is believed that maintaining these parameters generally constant over a range of power being delivered to the focusing spot would reduce the number of parameters to be considered in a laser machining process.
3.390625
3
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The role of Hydrotaea irritans in the transmission of summer mastitis. A series of experiments to investigate the possible role of the sheep head fly, Hydrotaea irritans, in the transmission of summer mastitis is reported. These showed that the pathogens Actinomyces pyogenes and Peptococcus indolicus may be harboured in the gut of the fly for up to 96 h following a contaminated meal; A. pyogenes survived on the surface of the fly for a similar period. H. irritans fed on the pathogens can contaminate a subsequent meal by regurgitation. However, no infections resulted from repeated exposure of the teats of heifers or cows to H. irritans fed on blood containing A. pyogenes and P. indolicus or on pus from a case of summer mastitis. In these experiments the frequency of feeding of the flies on the teat was high but subsequent bacterial contamination of the teat skin was low. Artificial contamination of the teat skin with greater than 10(6) cfu A. pyogenes led to a low incidence of mastitis even in the absence of cutaneous damage. Repeated applications of lower doses (less than 10(4) cfu) did not produce infection.
3
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Q: Four stages in C compiler I was trying to understand the basic flow in the C program. When the C code runs there are four stages of C code building process which utilizes different ‘tools’ such as a preprocessor, compiler, assembler, and linker. Finally, we get executable/.hex file from .c file. what is the role of the linker in C compiler.? I have run the .o file and executable. Both file giving same output. File obtained in differnt stage [linux@In23 toolchin]$ ls test test.asm test.c test.i test.o test.s [linux@In23 toolchin]$ ./test.o Hello World [linux@In23 toolchin]$ ./test Hello World A: The test.o is not an object file, you probably only changed the output-name. Since you are using Linux, you probably used either gcc or clang. In those, you generate an object file by specifying the "-c" flag. The linker can then take many of those object files and combine them into an executable.
3.21875
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Mobile communication devices, such as cellular telephones, transmit and/or receive data using various protocols to communicate remotely. Other portable devices such as laptop computers, tablet computers, portable game consoles and even watches may also include components that receive and transmit data, which makes them further examples of communication devices that are mobile. Such mobile communication devices generally include a subscriber identity/identification module (SIM) card, which is an integrated circuit used to store codes that identify and authenticate subscribers across mobile communication networks. A “subscription” may include services to which the subscriber by way of a mobile device has access. For example, a telephone number and the communications using that number are part of a subscription accessed using a SIM card. Subscriptions may use various communication standards, such as long term evolution (LTE), global system for mobile communications (GSM), general packet radio service (GPRS), enhanced data rates for GSM evolution (EDGE), universal mobile telecommunications system (UMTS), generic radio access network (GRAN), evolution-data optimized (1×/DO), and wideband code division multiple access (WCDMA) and code division multiple access (CDMA) to communicate across mobile communication networks. Some mobile devices may include more than one SIM card in order to maintain more than one subscription. For example, dual SIM mobile devices include two SIM cards and quad SIM mobile devices include four SIM Cards. In this way, a single mobile device may use different telephone numbers and maintain separate bills. Also, by using multiple SIM cards a user my keep business subscriptions separate from personal subscriptions, take advantage of different pricing/service plans or have an additional SIM card specific to a another country or region. While having multiple SIM cards in one device has its advantages, dual SIM devices consume more power than their single SIM counterparts, and quad SIM devices tend to consume significantly more power than dual SIM devices, which reduces their performance and is generally undesirable. Configuring dual SIM mobile devices to have two SIM cards that use a common radio frequency (RF) circuit (referred to as an “RF chain”) to communicate reduces the number of transceivers to one, which may save power. Similarly, Quad-SIM devices may have just two RF chains to support the four SIM cards (i.e., enable wireless communications via the subscriptions supported by each of the SIM cards). However, such configurations mean that one of the SIM cards must enter an out-of-service state when the other SIM card enters a dedicated traffic state in which the subscription associated with that SIM card is engaged in supporting communications over the single RF chain of the mobile device.
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Chemical structure and biological activity of endotoxins (lipopolysaccharides) and lipid A. Lipopolysaccharides (endotoxins) of gram-negative bacteria consist of two components with distinct physico-chemical character: a heteropolysaccharide and a covalently linked lipid, termed lipid A. Chemically, lipid A is made up of acylated glucosamine disaccharides, which are interlinked by pyrophosphate bridges. Lipid A represents the toxic center of lipopolysaccharides. In rabbits, lipid A also induces pyrogen tolerance as well as pyrogen cross-tolerance. Fever tolerance can be passively transferred with serum from rabbits immunized with lipid A. The protective power of lipid A antiserum, however, is only expressed in amimals which have been pretreated with lipid A or lipopolysaccharide, indicating that other than humoral factors, perhaps cellular, also participate in endotoxin tolerance. Lipid A antiserum also prevents the local Shwartzman reaction in rabbits. The possible potency of lipid A antiserum to prevent other endotoxin effects such as lethal shock is presently investigated.
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Law of Sines The Law of Sines is the relationship between the sides and angles of non-right (oblique) triangles. Simply, it states that the ratio of the length of a side of a triangle to the sine of the angle opposite that side is the same for all sides and angles in a given triangle. In ∆ABC is an oblique triangle with sides a, b and c, then . To use the Law of Sines you need to know either two angles and one side of the triangle (AAS or ASA) or two sides and an angle opposite one of them (SSA). Notice that for the first two cases we use the same parts that we used to prove congruence of triangles in geometry but in the last case we could not prove congruent triangles given these parts. This is because the remaining pieces could have been different sizes. This is called the ambiguous case and we will discuss it a little later. Example 1: Given two angles and a non-included side (AAS). Given ∆ABC with A = 30°, B = 20° and a = 45 m. Find the remaining angle and sides. The Ambiguous Case If two sides and an angle opposite one of them is given, three possibilities can occur. (1) No such triangle exists. (2) Two different triangles exist. (3) Exactly one triangle exists. Consider a triangle in which you are given a, b and A. (The altitude h from vertex B to side , by the definition of sines is equal to b sin A.) (1) No such triangle exists if A is acute and a < h or A is obtuse and a ≤ b. (2) Two different triangles exist if A is acute and h < a < b. (3) In every other case, exactly one triangle exists. Example 1:No Solution Exists Given a = 15, b = 25 and A = 80°. Find the other angles and side. h = b sin A = 25 sin 80° ≈ 24.6 Notice that a < h. So it appears that there is no solution. Verify this using the Law of Sines. This contrasts the fact that the –1 ≤ sin B ≤ 1. Therefore, no triangle exists. Example 2:Two Solutions Exist Given a = 6. b = 7 and A = 30°. Find the other angles and side. h = b sin A = 7 sin 30° = 3.5 h < a < b therefore, there are two triangles possible. By the Law of Sines, There are two angles between 0° and 180° whose sine is approximately 0.5833, 35.69° and 144.31°. If B ≈ 35.69° If B ≈ 144.31° C ≈180° – 30° – 35.69° ≈ 114.31° C ≈ 180° – 30° – 144.31° ≈ 5.69° Example 3:One Solution Exists Given a = 22, b =12 and A = 40°. Find the other angles and side. a > b By the Law of Sines, B is acute. C ≈ 180° – 40° – 20.52° ≈ 119.48° By the Law of Sines, If we are given two sides and an included angle of a triangle or if we are given 3 sides of a triangle, we cannot use the Law of Sines because we cannot set up any proportions where enough information is known. In these two cases we must use the Law of Cosines.
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Q: Telephone number in spoken words Goal Write a program or function that translates a numerical telephone number into text that makes it easy to say. When digits are repeated, they should be read as "double n" or "triple n". Requirements Input A string of digits. Assume all characters are digits from 0 to 9. Assume the string contains at least one character. Output Words, separated by spaces, of how these digits can be read out loud. Translate digits to words: 0 "oh" 1 "one" 2 "two" 3 "three" 4 "four" 5 "five" 6 "six" 7 "seven" 8 "eight" 9 "nine" When the same digit is repeated twice in a row, write "double number". When the same digit is repeated thrice in a row, write "triple number". When the same digit is repeated four or more times, write "double number" for the first two digits and evaluate the rest of the string. There is exactly one space character between each word. A single leading or trailing space is acceptable. Output is not case sensitive. Scoring Source code with the least bytes. Test Cases input output ------------------- 0123 oh one two three 4554554 four double five four double five four 000 triple oh 00000 double oh triple oh 66667888 double six double six seven triple eight 19999999179 one double nine double nine triple nine one seven nine A: 8088 Assembly, IBM PC DOS, 164 159 156 155 bytes Binary: 00000000: d1ee 8a0c 03f1 53fd ac3a d075 0343 e2f7 ......S..:.u.C.. 00000010: 85db 741c 5f8a d043 f6c3 0174 0a57 bd64 ..t._..C...t.W.d 00000020: 0155 83eb 0374 0957 bd5d 0155 4b4b 75f7 .U...t.W.].UKKu. 00000030: 8ad0 2c2f 7213 518a f0b0 24b1 31bf 6a01 ..,/r.Q...$.1.j. 00000040: fcf2 aefe ce75 fa59 57e2 bc5a 85d2 740c .....u.YW..Z..t. 00000050: b409 cd21 b220 b402 cd21 ebef c364 6f75 ...!. ...!...dou 00000060: 626c 6524 7472 6970 6c65 246f 6824 6f6e ble$triple$oh$on 00000070: 6524 7477 6f24 7468 7265 6524 666f 7572 e$two$three$four 00000080: 2466 6976 6524 7369 7824 7365 7665 6e24 $five$six$seven$ 00000090: 6569 6768 7424 6e69 6e65 24 eight$nine$ Build and test executable using xxd -r from above, or download PHONE.COM. Unassembled listing: D1 EE SHR SI, 1 ; point SI to DOS PSP (80H) for input string 8A 0C MOV CL, BYTE PTR[SI] ; load input string length into CX 03 F1 ADD SI, CX ; move SI to end of input 53 PUSH BX ; push a 0 to signal end of output stack CHAR_LOOP: FD STD ; set LODS direction to reverse AC LODSB ; load next char from [SI] into AL, advance SI 3A D0 CMP DL, AL ; is it same as previous char? 75 03 JNZ NEW_CHAR ; if not, it's a different char 43 INC BX ; otherwise it's a run, so increment run length E2 F7 LOOP CHAR_LOOP ; move on to next char NEW_CHAR: 85 DB TEST BX, BX ; is there a run greater than 0? 74 1C JZ GET_WORD ; if not, look up digit name 5F POP DI ; get name for the current digit 8A D0 MOV DL, AL ; save current char in DL 43 INC BX ; adjust run count (BX=1 means run of 2, etc) F6 C3 01 TEST BL, 1 ; is odd? if so, it's a triple 74 0A JZ IS_DBL ; is even, so is a double 57 PUSH DI ; push number string ("one", etc) to stack BD 0164 MOV BP, OFFSET T ; load "triple" string 55 PUSH BP ; push to stack 83 EB 03 SUB BX, 3 ; decrement run count by 3 74 09 JZ GET_WORD ; if end of run, move to next input char IS_DBL: 57 PUSH DI ; push number string to stack BD 015D MOV BP, OFFSET D ; load "double" string 55 PUSH BP ; push to stack 4B DEC BX ; decrement by 2 4B DEC BX 75 F7 JNZ IS_DBL ; if not end of run, loop double again GET_WORD: 8A D0 MOV DL, AL ; save current char into DL 2C 2F SUB AL, '0'-1 ; convert ASCII char to 1-based index 72 13 JB NOT_FOUND ; if not a valid char, move to next 51 PUSH CX ; save outer loop counter 8A F0 MOV DH, AL ; DH is the index to find, use as scan loop counter B0 24 MOV AL, '$' ; word string is $ delimited B1 31 MOV CL, 031H ; search through length of word data (49 bytes) BF 016A MOV DI, OFFSET W ; reset word data pointer to beginning FC CLD ; set DF to scan forward for SCAS SCAN_LOOP: F2/ AE REPNZ SCASB ; search until delimiter '$' is found in [DI] FE CE DEC DH ; delimiter found, decrement counter 75 FA JNZ SCAN_LOOP ; if counter reached 0, index has been found 59 POP CX ; restore outer loop position 57 PUSH DI ; push string on stack NOT_FOUND: E2 BC LOOP CHAR_LOOP ; move to next char in input OUTPUT_STACK: 5A POP DX ; get string from top of stack 85 D2 TEST DX, DX ; it is the last? 74 0C JZ EXIT ; if so, exit B4 09 MOV AH, 09H ; DOS display string function CD 21 INT 21H ; write string to console B2 20 MOV DL, ' ' ; load space delimiter B4 02 MOV AH, 02H ; DOS display char function CD 21 INT 21H ; write char to console EB EF JMP OUTPUT_STACK ; continue looping EXIT: C3 RET ; return to DOS D DB "double$" T DB "triple" W DB "$oh$","one$","two$","three$","four$","five$","six$","seven$","eight$","nine$" TL;DR: The input string is read right to left to make it easier to find a triple. The output is pushed onto the x86 stack to simplify reversing out the display order and also facilitate rearranging the "double" and "triple" words to precede the digit's name. If the next digit is different than the last, the name is looked up in the list of words and pushed on to the stack. Since there's no formal concept of an "indexed array of variable-length strings" in machine code, the list of words is scanned i (the word's index) number of times for the string delimiter ($) to find the corresponding word. Helpfully, x86 does have a pair of short instructions (REPNZ SCASB which is similar to memchr() in C), that simplifies this (thanks CISC!). If the digit is the same as the previous one, the counter for the length of a "run" is incremented and continues looping leftward on the input. Once the run is over, the digit's name is taken from the stack since it will need to placed after the "double" or "triple" for each grouping. If the length of the run is odd (and run length is > 1), the digit's name followed by the string "triple" is pushed to the stack and the run length is reduced by 3. Since the run length will now be even, the step is repeated for "double" until the run length is 0. When the input string has reached the end, the stack is dumped out with each saved string written to the screen in reverse order. I/O: A standalone PC DOS executable, input from command line output to console. Download and test PHONE.COM. A: 05AB1E, 53 52 51 50 49 bytes γε€T2äθ¬MÊi¨₃1ǝR]˜“Šç€µ‚•„í†ìˆÈŒšï¿Ÿ¯¥Š‹¶½¿“#s踻 Try it online! Explanation: γ # split input in groups of consecutive equal digits ε ] # for each group €T # add a 10 before each digit (66 -> [10, 6, 10, 6]) 2äθ # keep only the second half of that list ¬MÊi ] # if the first element is not the maximum ¨ # drop the last element ₃1ǝ # replace the second element with 95 R # reverse the list ˜ # flatten “...“ # compressed string: "oh one two ... nine double triple" # # split on spaces sè # index (wraps around, so 95 yields "triple") ¸» # join with spaces A: 05AB1E, 61 56 53 52 51 bytes γvyDg;LàäRv… ‹¶½¿#yg蓊瀵‚•„í†ìˆÈŒšï¿Ÿ¯¥Š“#yè])áðý -9 bytes thanks to @Grimy. Try it online or verify all test cases. Explanation: γ # Split the (implicit) input into substrings of equal adjacent characters # i.e. "199999991779" → ["1","9999999","1","77","9"] v # Loop over each substring `y`: Dg # Get the length of a copy of the substring ; # Halve it L # Create a list in the range [1, length/2], where odd lengths are # automatically truncated/floored # i.e. "1" (length=1) → 0.5 → [1,0] # i.e. "9999999" (length=7) → 3.5 → [1,2,3] à # Pop and push the maximum of this list y ä # Divide the string into that many parts # → ["1"] # → ["999","99","99"] R # Reverse the list # → ["99","99","999"] v # Inner loop over each item `y`: … ‹¶½¿ # Push dictionary word: " double triple" # # Split it on spaces: ["","","double","triple"] yg # Get the length of the current item `y` è # And use it to (0-based) index into the list “Šç€µ‚•„í†ìˆÈŒšï¿Ÿ¯¥Š“ # Push dictionary string "oh two three four five six seven eight nine" # # Split it on spaces: ["oh","two","three",...,"nine"] yè # Use `y` to index into the string-list (with automatic wrap-around, # so since there are 10 words, it basically indexes with a single digit # due to an implicit modulo-10) # i.e. "77" → "seven" ] # Close both loops ) # Wrap all values on the stack into a list á # Only keep letters, which removes the empty strings from the list ðý # And join the list on spaces # (after which the result is output implicitly) See this 05AB1E tip of mine (section How to use the dictionary?) to understand why … ‹¶½¿ is " double triple" and “Šç€µ‚•„í†ìˆÈŒšï¿Ÿ¯¥Š“ is "oh two three four five six seven eight nine".
3.46875
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It has already been well recognized that there is a need for a plant watering device which will ensure an adequate supply of water to a plant after a considerable lapse of time and without human intervention, after initial setting up of the device. Thus, for example, a person leaving his or her dwelling for a period of time, for example for the purpose of a vacation, often requires to ensure that a plant in the dwelling is adequately irrigated during that period of time but, nevertheless, frequently desires to avoid overwatering of the plant and, also, to avoid granting access to another person to the dwelling for the purpose of watering the plant. Various attempts have been made in the past to provide a watering device which fulfills such a purpose by providing a constant, possibly very slow, supply of water to a plant, or by effecting a delayed supply of water to the plant. For example, one prior watering device comprises a tray to be placed under a pot containing the plant, with a wick extending from the tray through the base of the pot and terminating in a potting mix within the pot, so that water is drawn up the wick by a wicking action. Another prior device comprises a large tray fitted with a porous styrofoam base for a plant pot and, in that case, moisture percolated up to the pot from the tray by capillary action trough the styrofoam base. Another prior suggestion is a cone shaped device made of pottery, which is glazed at the open end of the cone-shaped device, the opposite, pointed end of the device being closed but remaining unglazed, so that when the cone is inverted and pushed into the soil, and the inside of the device is filled with water, the water is slowly released through the pointed end of the device to water the plant and, thereby, to prevent it from drying out. It will be appreciated that the above-described devices are intended to effect constant watering of a plant, rather than providing a delayed supply of water to the plant after a period of time during which no watering occurs. A further prior art watering device is shown in U.S. Pat. No. 267,296, which teaches a self-irrigating flower pot or vase in which apertures allow water to pass from a reservoir into a saucer and then into the pot. Evaporation from the saucer and absorption of water in the pot cause the liquid level in the saucer to fall below the apertures, which allows further water to flow from the reservoir. Once again, this prior device constantly waters the pot. U.S. Pat. No. 3,125,255, issued Mar. 17, 1964 to B. Kaiser, shows the use of evaporation from an auxiliary reservoir to control air flow into a main reservoir and, thus, to control the outflow of water from the main reservoir. More particularly, according to the teachings of this prior device, evaporation from a so-called water receiver uncovers the lower end of a tube, to allow air to flow into a main container, which in turn allows water to flow therefrom through an outlet. While the device shown in the aforesaid U.S. Pat. No. 3,125,255 effects delayed watering of a plant or the like, by employing evaporation in a separate water chamber to delay the onset of irrigation, as described above, it nevertheless simply allows a single flow of water from the main container at a delayed period of time but in a continuous manner, and does not in any way enable an intermittent, i.e. repeated, watering action to be effected. Further prior art watering devices are shown in U.S. Pat. Nos. 3,438,575; 4,060,934; 4,085,546; 4,121,608; 4,241,538 and 4,542,762.
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Q: quiz about bit related topics i have following quiz: Let x be an integer larger than the odd number q. Change the value of x using the following rule if x is even then x / 2 else x – q until x becomes smaller than q If the final value of x is zero, what can you say about the original input value? I am thinking about one thing: if x is odd or x=2*k+1 and we are subtract also odd number, we get even. Also I want to note, that unless x is power of 2, at some step dividing by 2, we get odd number. Let take q=11; x>11;let's take x=23; because x=23 is odd, we will have x=x-q x=23-11=12; now x is even so we will have x/2=6<11, so here we can't determine which value of x is about,but if x=22, then we will have x=x/2=11 x=11 is odd, so we will have x-q=0--> it means that x is multiple of q, but which one odd or even number? Let's take x=33; x is odd so x=x-11=22 it is even x=x/2=11, it is odd so x-q=0; no does it means that x is multiple of q? A: Yes, it is apparently that x is multiple of q.
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A cataract is “any opacity which establishes in the crystalline lens of the eye or its envelope.” Cataracts create a range of factors, with one of the most typical element being the lasting direct exposure to ultraviolet light. Cataracts could additionally create from innovative age or additional impacts of illness such as diabetes mellitus. An outcome of denaturation (the conversion of DNA from the double-stranded to the single-stranded state; splitting up of the hairs is frequently completed by home heating) of healthy lens proteins, there are numerous hereditary aspects which are likewise understood to play a significant function inclining a specific to cataracts. As discussed over with progressing age the occurrence of cataracts ends up being even more leading. Cataract development is anticipated in any private over the age of 70 (50% of all individuals in between the ages of 65 as well as 74 & about 70% of those over 75). Cataracts are most frequently assisted through a surgical treatment called cataract surgery. The surgical procedure intends to recover the eye back to its initial state by getting rid of any cataracts that are existing. We’re just provided one collection of 2 eyes. Caring for them is very essential. This could suggest straightforward preventative measures such as putting on sunglasses to stop our eyes from aspects such as ultraviolet light, wind, as well as from obtaining fragments in the eye that could harm or lenses. Reflexology for eyes can also be used.
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About the Author Historian Christopher Hamner teaches at George Mason University, serves as Editor-in-Chief of Papers of the War Department, 1784-1800, and is the author of Enduring Battle: American Soldiers in Three Wars, 1776-1945. American Resistance to a Standing Army Question Quote from Madison: "The means of defence against foreign danger, have been always the instruments of tyranny at home. Among the Romans it was a standing maxim to excite a war, whenever a revolt was apprehended. Throughout all Europe, the armies kept up under the pretext of defending, have enslaved the people." I understand what he means, but can you give some specific examples of which events Madison was talking about. Can you give other ancient examples where foreign wars are used as a type of diversion? Answer In June of 1787, James Madison addressed the Constitutional Convention in Philadelphia on the dangers of a permanent army. “A standing military force, with an overgrown Executive will not long be safe companions to liberty,” he argued. “The means of defense against foreign danger, have been always the instruments of tyranny at home. Among the Romans it was a standing maxim to excite a war, whenever a revolt was apprehended. Throughout all Europe, the armies kept up under the pretext of defending, have enslaved the people.” That Madison, one of the most vocal proponents of a strong centralized government—an author of the Federalist papers and the architect of the Constitution—could evince such strongly negative feelings against a standing army highlights the substantial differences in thinking about national security in America between the 18th century and the 21st. While polls today generally indicate that Americans think of the military in glowing terms (rightly associating terms like “sacrifice,” “honor,” “valor,” and “bravery” with military service), Americans of the 18th century took a much dimmer view of the institution of a professional army. A near-universal assumption of the founding generation was the danger posed by a standing military force. Far from being composed of honorable citizens dutifully serving the interests of the nation, armies were held to be “nurseries of vice,” “dangerous,” and “the grand engine of despotism.” Samuel Adams wrote in 1776, such a professional army was, “always dangerous to the Liberties of the People.” Soldiers were likely to consider themselves separate from the populace, to become more attached to their officers than their government, and to be conditioned to obey commands unthinkingly. The power of a standing army, Adams counseled, “should be watched with a jealous Eye.” Experiences in the decades before the Constitutional Convention in 1787 reinforced colonists’ negative ideas about standing armies. Colonials who fought victoriously alongside British redcoats in the Seven Years’ War concluded that the ranks of British redcoats were generally filled with coarse, profane drunkards; even the successful conclusion of that conflict served to confirm colonists’ starkly negative attitudes towards the institution of a standing army. The British Crown borrowed massively to finance the conflict (the war doubled British debt, and by the late 1760s, fully half of British tax revenue went solely to pay the interest on those liabilities); in an effort to boost its revenues, Parliament began to pursue other sources of income in the colonies more aggressively. In the decade before the Declaration of Independence, Parliament passed a series of acts intended to raise money within the colonies. The power of a standing army, Adams counseled, “should be watched with a jealous Eye.” That legislation further aggravated colonists’ hostility towards the British Army. As tensions between the colonies and the crown escalated, many colonists came to view the British army as both a symbol and a cause of Parliament’s unpopular policies. Colonists viewed the various revenue-generating acts as necessitated by the staggering costs associated with maintaining a standing army. The Quartering Act, which required colonists to provide housing and provisions for troops in their own buildings, was another obnoxious symbol of the corrupting power represented by the army. Many colonists held the sentiment that the redcoats stationed in the colonies existed not to protect them but to enforce the king’s detestable policies at bayonet-point. No event crystallized colonists’ antagonism towards the British army more clearly than what became known as the Boston Massacre. In March 1770, British regulars fired into a crowd of civilians, killing five. That event provided all the proof the colonists needed of the true nature of the redcoats’ mission in the colonies. Six years later, the final draft of the Declaration of Independence contained numerous references to King George’s militarism (particularly his attempts to render the army independent of civilian authority, his insistence on quartering the troops among the people, and his importation of mercenaries to “compleat the works of death, desolation, and tyranny”); by the end of the War of Independence, hatred of a standing army had become a powerful and near-universal tradition among the American people; the professional British army was nothing less than a “conspiracy against liberty.” Colonists’ experiences with British troops, and the convictions that sprang from them, help explain Madison’s reference to armies having traditionally “enslaved” the people they were commissioned to defend. After winning their political independence, the victorious colonies faced the difficult task of providing for their own security in the context of a deep-seated distrust of a standing military. Madison’s language reflected a common concern that the maintenance of a standing army in the new United States would place [financial] burdens on the young government [of the United States]. Madison’s use of the imagery of slavery points to the multiple meanings of that term in the 18th century. In Madison’s statement to the Convention, it referred not to the literal notion of armies marching the citizenry through the streets in shackles but to a kind of metaphorical slavery. The immense costs necessary to raise and maintain a standing army (moneys required for pay, uniforms, rations, weapons, pensions, and so forth) would burden the populace with an immense and crippling tax burden that would require the government to confiscate more and more of the citizenry’s wealth in order to meet those massive expenses. Madison’s language reflected a common concern that the maintenance of a standing army in the new United States would place similar burdens on the young government; their experiences with the British army under Parliament in the 1760s and 1770s likewise led to concerns that the executive would use a standing army to force unpopular legislation on an unwilling public in similar fashion. Other members of the founding generation worried that an armed, professional force represented an untenable threat to the liberty of the people generally. Throughout history, the threat of military coup—governments deposed from within by the very forces raised to protect them—has been a frequent concern. In 1783, Continental Army officers encamped at Newburgh circulated documents that leveled a vague threat against Congress if the government continued its refusal to pay the soldiers. Historians generally conclude that a full-blown coup d’etat was never a realistic possibility, but the incident did little to assuage contemporary concerns about the dangers posed by a standing army. The experience with professional armies during the 40 years before the Constitutional Convention, and the values that sprang from those experiences, helps explain why the founders never seriously considered maintaining the Continental Army past the end of the War of Independence. The beliefs that grew organically from their experiences with the British also help explain Madison’s passionate anti-military rhetoric (he would later refer to the establishment of a standing army under the new Constitution as a “calamity,” albeit an inevitable one); together, they cast a long shadow over the debates surrounding the kind of military the new nation would provide for itself. 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Eleanor of England, Countess of Leicester Eleanor of England (also called Eleanor Plantagenet and Eleanor of Leicester) (1215 – 13 April 1275) was the youngest child of John, King of England and Isabella of Angoulême. Early life At the time of Eleanor's birth at Gloucester, King John's London was in the hands of French forces, John had been forced to sign the Magna Carta and Queen Isabella was in shame. Eleanor never met her father, as he died at Newark Castle when she was barely a year old. The French, led by Prince Louis the Lion, the future Louis VIII, were marching through the south. The only lands loyal to her brother, King Henry III of England, were in the Midlands and southwest. The barons ruled the north, but they united with the royalists under William Marshal, 1st Earl of Pembroke, who protected the young king Henry, and Louis was defeated. Before William Marshal died in 1219 Eleanor was promised to his son, also named William. They were married on 23 April 1224 at New Temple Church in London. The younger William was 34 and Eleanor only nine. He died in London on 6 April 1231, days before their seventh anniversary. There were no children of this marriage. Eleanor had brought a dowry of 10 manors and 200 pounds per year to this marriage. According to the law of the time, widows were allowed to retain one third of the estates of the marriage. However, her brother-in-law Richard took all of the estates and sold many, including her dowry, to pay William's debts. Eleanor strove for many years to try and recover her lost property. The widowed Eleanor swore a holy oath of chastity in the presence of Edmund Rich, Archbishop of Canterbury. Simon de Montfort Seven years later, she met Simon de Montfort, 6th Earl of Leicester. According to Matthew Paris, Simon was attracted to Eleanor's beauty and elegance as well as her wealth and high birth. They fell in love and married secretly on 7 January 1238 at the King's chapel in Westminster Palace. Her brother King Henry later alleged that he only allowed the marriage because Simon had seduced Eleanor. The marriage was controversial because of the oath Eleanor had sworn several years before to remain chaste. Because of this, Simon made a pilgrimage to Rome seeking papal approval for their union. Simon and Eleanor had seven children: Henry de Montfort (November 1238 – 1265) Simon de Montfort the Younger (April 1240 – 1271) Amaury de Montfort (1242/1243–1300) Guy de Montfort, Count of Nola (1244–1288) Joanna, born and died in Bordeaux between 1248 and 1251 Richard de Montfort (1252–1281) Eleanor de Montfort Princess of Wales (1258–1282) During the Second Barons' War, Simon de Montfort's victory at the Battle of Lewes in 1264 led to him becoming de facto ruler of England. He tried to set up a reformed government, including the first parliament elected by citizens of the towns, but was unable to retain the support of the other barons. Several switched sides to the royalist cause; Montfort was defeated at the Battle of Evesham on 4 August 1265, where he was killed along with his son. Eleanor fled to exile in France where she became a nun at Montargis Abbey, a nunnery founded by her deceased husband's sister Amicia, who remained there as abbess. There she died on 13 April 1275, and was buried there. She was well treated by Henry, retained her incomes, and her proctors were allowed to pursue her litigation concerning the Leicester inheritance in the English courts; her will and testament were executed without hindrance. Through her son Guy, Eleanor was an ancestor of Elizabeth Woodville, queen consort of Edward IV. Eleanor's daughter, Eleanor de Montfort, was married, at Worcester in 1278, to Llywelyn ap Gruffudd, Prince of Wales. She would die giving birth to their only child, Gwenllian of Wales. After the conquest of Wales, Gwenllian was imprisoned by Edward I of England, her mother's first cousin, at Sempringham priory, where she died 1337. Fiction Eleanor appears as a major character in Sharon Kay Penman's novel Falls the Shadow, where she is called Nell. Eleanor is the main character in Virginia Henley's historical romance The Dragon and the Jewel, which tells of her life from just before her marriage to William Marshal to right before the Battle of Lewes in 1264. Her romance and marriage to Simon de Montfort are much romanticized in this novel, especially since in real life Simon is killed the year following the Battle of Lewes and the pair had already had all 7 of their children; in the book, Eleanor and Simon have only just had their first two sons. Eleanor makes a second appearance in Henley's The Marriage Prize. Her role in the book is that of the legal guardian to her niece, Rosamond Marshal. Ancestors Sources Notes Category:1215 births Category:1275 deaths Category:13th-century English people Category:13th-century English women Category:English princesses Category:English Roman Catholic religious sisters and nuns Category:House of Plantagenet
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rice Introduction rice, cereal grain ( Oryza sativa ) of the grass family (Graminae), probably native to the deltas of the great Asian rivers—the Ganges, the Chang (Yangtze), and the Tigris and Euphrates. The plant is an annual, from 2 to 6 ft (61–183 cm) tall, with a round, jointed stem; long, pointed leaves; and edible seeds borne in a dense head on separate stalks. Wild rice is obtained from a different grass plant.
3.140625
3
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Second Perek, Third Mishna Expanded Translation This woman has one pair of undesignated birds. This woman has two pair. This woman has three pair. This woman has four pair. This woman has five pair. This woman has six pair. This woman has seven pair. One bird flew from the group belonging to the first woman to that of the second. Then a bird (not necessarily the same bird) flew from the second group to the third woman's group. Then a bird flew from the third group to the fourth woman's group, then a bird flew from the fourth group to the fifth woman's group. Then a bird flew from the fifth group to the sixth woman's group. Then a bird flew from the sixth group to the seventh woman's group. Then one bird flew back from each group to the next smaller group. Each bird disqualifies one pair when it leaves a group to a larger group and it also disqualifies one pair when it returns from a group to a smaller group. The first and second women have nothing that can be brought. The third woman (whose group started with three pair) has one pair that can be brought. The fourth woman has two pair. The fifth woman has three pair. The sixth woman has four pair. The seventh woman has six pair. Only one bird left the seventh group (into the sixth). Therefore, unlike most of the groups, in which two pair are disqualified, one pair is disqualified in the seventh group. The seventh woman is then left with six pair to be brought. Example of the Case of the Mishna The First Porach V'chozar Each of seven women had a different number of kinim. The first woman had one kain (two birds), the second, two kinim, and so on. First, one bird flew out of the first group to the second, then one flew from the second to the third, and so on, until the seventh. (None yet flew out of the seventh.) Then a bird flew out of group seven to group six, then one flew from group six to five, and so on to group one. (But a second bird did not fly out of group one.) It is possible that only one bird did all the travelling in each direction. It is possible that each flight was done by a different bird. It is possible that some of the flights were done by one bird and some by other birds. Result Each group has the same number of birds it started with. One bird has flown out of groups one and seven, and two birds left groups two through six. Although each group has the same number of birds as it started with, one or two now in each group might not have originated in that group. [Diagram 9] Dinim Din of the First Group No korbonos may be brought. Reason Either bird now in the first group might be an original member of the group. It may not be brought as a Chatos for perhaps its partner, which might now be in another group, will be brought as a Chatos. It may not be brought as an Olah because its partner might be brought as an Olah. [Diagram 14, meant to be viewed later] Din of the Second Group None of the four birds is brought. Reason None of the birds may be brought as a Chatos because the two birds that flew out might both be brought as Chato'os by other women. None may be brought as Olos because the two that flew out might be brought as Olos by other women. We want to assure that no more than two of the original birds of the second group will be Chato'os, nor will more than two be Olos. Comment In fact, one of the two birds that flew out of the second group flew into the first group. Since none of the birds now in the first group will be offered, we need not be concerned that that bird will be a Chatos or an Olah. However, in order to avoid confusion the Rabonon said that we should treat this bird as if it flew among birds that would become korbonos. (Tosfos, Maseches Yuma Daf 65:2, dibbur hamas'chil "umishoom gzaira yomusu.") One possible understanding of this rule is that when two birds fly out of one group, and one mingles with birds that are offered and the other with birds that are not, we consider it as if both flew among birds that are offered. [Diagram 15] Din of the Third Group One bird is brought as a Chatos, another as an Olah. The remaining four birds are not brought. Reason We cannot bring two Chato'os because other women might bring the two birds that flew out as Chato'os. No more than three Chato'os may be brought from the original group of six birds. We cannot bring two Olos because the two birds that flew out might become Olos. No more than three Olos may be brought from the original group. Comment In fact, the bird that flew to group two will not be brought because none of the second group is brought. The Rabonon treat this case as if both birds flew where there was a risk that they would be brought, as we treated the second group. [Diagram 16] Din of the Fourth, Fifth, and Sixth groups We bring four birds of the eight in the fourth group, six of the ten in the fifth group, and eight of the twelve in the sixth group. Half of those brought are Chato'os, and half are Olos. Reason The din follows the reasoning for the second and third groups. Namely, two birds left each group. We reduce by two the number of Chato'os to be brought from each group, in case both birds that flew out are brought as Chato'os. We also reduce by two the number of Olos from each group, in case both birds that left are brought as Olos. That is, four fewer birds are brought than the original number. This reduces the number of korbonos from eight to four, from ten to six, and from twelve to eight in the respective groups. [Diagrams 10, 11, and 12] Din of the Seventh Group We bring twelve of the fourteen birds, six as Chato'os and six as Olos. Reason Only one bird left this group. Since the bird that flew out might be brought as a Chatos, we reduce the number of Chato'os brought from this group by one. Since it might be brought as an Olah, we bring one Olah less. That is, six birds are Chato'os, six are Olos, and two are not brought at all. [Diagram 13] Comment The dinim of the first through seventh groups are applications of the principle stated following Mishna Bais, that each bird flying out of a group reduces by two the number of birds that can be brought from that group. Expanded Translation Then, starting with the third group, a bird flew out of each group into the next larger group, and one bird flew back from group seven through four into the next smaller group. Each bird disqualifies one pair when it leaves a group for a larger group, and disqualifies a pair when it returns from a group to a smaller group. The third and fourth women have nothing that can be brought. The fifth woman, who after the first porach v'chozar had three pair, now has one pair. The sixth woman has two. The seventh has five. Example of Case of the Mishna The Second Porach V'chozar At the end of the first porach v'chozar all the birds in the first and second groups are disqualified from being korbonos. Therefore, birds will now move only among groups three through seven, as the end of the Mishna clarifies. As this part begins, the third woman can bring two birds (one kain of her original three), the fourth woman can bring four birds (two kinim of four), the fifth can bring six (three kinim of five), the sixth can bring eight (four kinim of six), the seventh can bring twelve (six kinim of seven). Now one additional bird flew from the third group to the fourth group,one flew from the fourth group to the fifth, and so on until the seventh group. (No additional bird flew yet out of the seventh.) Then a bird flew out of group seven to group six, then one flew from group six to five, and so on until group three. (No additional bird flew from the third group to the second.) Result Each woman has the same number of birds she started with. One bird has flown out of group three, in addition to the two that left earlier, for a total loss of three. Groups four through six each lost two birds in addition to the two lost earlier, for a total of four lost. Group seven lost one earlier and one now for a total loss of two. (As many birds joined each group as the group lost.) [Diagram 17] Dinim Din of the Third Group No korbonos are brought. Reason The principle of Mishna Bais continues to be applied, reducing by two the number of birds that can be brought for each bird that left the group. The third group has lost three of its six birds. They might all be brought as Chato'os by other women, leaving no Chato'os to be brought by the owner of this group. The three might all be brought as Olos, leaving no Olos to be brought. [Diagram 18] Din of the Fourth, Fifth and Sixth groups No korbonos are brought from group four, one Chatos and one Olah are brought from group five, and two Chato'os and two Olos are brought from group six. Reason Each group has lost four of its birds. This reduces the number of korbonos brought from each group by eight, two for each bird that flew out, by the principle stated following Mishna Bais. That is, if the four birds that flew out of each group are all brought as Chato'os, then four fewer Chato'os should be brought. If the four that left are brought as Olos, four fewer Olos should be brought. This disqualifies all eight birds in group four, eight of the ten birds in group five, and eight of the twelve in group six. Comment In fact, some of the birds flew to groups that are now completely disqualified. The Rabonon treat these cases as if all the birds might be brought as part of other groups, as in the comment on the din of the second group. [Diagrams 10, 20, and 21] Din of the Seventh Group Ten of the original fourteen are brought, five as Chato'os and five as Olos. Reason Group seven has lost a total of two birds. (Groups four through six each lost two birds to the next larger group and two to the next smaller group. But group seven only lost two birds to the next smaller group, group six. None flew into a larger group as there is no larger group.) Since both birds might be brought as Chato'os, we bring two fewer Chato'os, and since they might both be Olos, we bring two fewer Olos. This disqualifies four of the fourteen original birds, another application of the principle stated following Mishna Bais. [Diagram 22] Expanded Translation A bird flew out of group five to group six and from group six to group seven, and one bird flew back from seven to six and six to five. It disqualifies one pair when it leaves each group for a larger group, and it disqualifies one pair when it returns. The fifth and sixth women have nothing to be brought. The seventh woman has four pair. And some say that the seventh woman does not lose anything as a result of the third porach v'chozar and continues to be able to bring five pair. Example of the Case of the Mishna The Third Porach V'chozar At the end of the second porach v'chozar all the birds in the first through fourth groups are disqualified from being korbonos. Therefore birds will now move only among groups five through seven. As this part begins, the fifth woman can bring two birds (one kain of the original five), the sixth woman can bring four birds (two kinim of the original six), and the seventh woman can bring ten birds (five kinim of the original seven). Now one bird flew from group five to the sixth group and one flew from six to seven. (None flew out of the seventh.) Then a bird flew out of group seven to group six, and one flew out of group six to group five. (None flew out of five.) Result Each woman has the same number of birds that she started with. However, as many as six birds that are now in a group might not be originally from that group. [Diagram 23] Dinim Din of the Fifth Group None of the birds is brought. Reason A total of five birds have flown out. They might all be brought as Chato'os, leaving no more Chato'os to bring. If they were all brought as Olos no more Olos can be brought from this group. [Diagram 24] Din of the Sixth Group None of the birds is brought. Reason A total of six birds have flown out. They might all be brought as Chato'os, leaving no more Chato'os to be brought. They might all be brought as Olos, leaving no more Olos to be brought. Comment As in previous cases, some of the birds that left groups five and six flew to groups from which no korbonos are being brought. The Rabonon treat these birds as if they might have been brought, as noted earlier. [Diagram 25] Din of the Seventh Group (First opinion) Four birds are brought as Chato'os and four as Olos. Reason A total of three birds have flown out of this group. In truth, none of those birds will be brought as korbonos, because all the birds in all the other groups have by now been disqualified. However, the Rabonon have legislated (as discussed above with respect to the din of the second group) that we treat the remaining birds in the group as if those that flew out will be brought as korbonos. If all three were brought as Chato'os, group seven would have four more Chato'os to bring. If the three were brought as Olos, group seven would have four more Olos to bring. [Diagram 26] Din of the Seventh Group (Second opinion) Five birds are brought as Chato'os and five are brought as Olos (just as was the din before this third porach v'chozar). Reason Of the total of three birds that left group seven, two flew into group six when it was possible for the owner of group six to bring them as korbonos. Therefore, the number of kinim brought from group seven was reduced by two. That is, only five Chato'os and five Olos could still be brought. However, we are not concerned that the third bird that flies from group seven will be brought as a Chatos or an Olah, since, by now, all the birds in group six are disqualified (as explained above). Therefore, the third bird to leave group seven does not disqualify a third pair from group seven. According to this opinion, the Rabonon did not treat the third bird as if it might be brought by another woman. It appears that the Rabonon were concerned only about a case where more than one bird left a group and one of them might truly be brought. But in the case of group seven in the third porach v'chozar, only one bird leaves group seven, and there is no chance it will be brought. [Diagram 27] Expanded Translation If a bird flew from a group that must be left to die (because the entire group is disqualified), all those in the group into which the bird flew must be left to die. Example of the Case of the Mishna After the first porach v'chozar all the birds in groups one and two are disqualified. Then a bird moved from group one to group two to group three and so on as in the first porach v'chozar. Result The disqualified bird that left group two might have remained in group three (and the bird that moved from group three to group four might be a different bird) or it might have continued moving from group to group and ended in groups four, five, six, or seven. Din None of the birds of any group may be brought. Reason Each bird in each group might be the disqualified bird that originated in group one or two. Comment The Mishna here is clarifying why, in the cases of the second and third porach v'chozar, no birds flew from groups one through four after those groups were completely disqualified.
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3
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Guadeloupeans who survived the deadly crackdown of May 1967 describe the legacy of distrust of the French state. Pointe-a-Pitre, Guadeloupe – “Without warning, they shot me. I fell to the ground and played dead.” It was May 26, 1967. Solange Coudrieux, a Guadeloupean teacher, was on his way home when he got caught up in a protest in Pointe-a-Pitre, Guadeloupe’s capital. Coudrieux was one of the many Guadeloupeans to be shot by French police that day. “There was no curfew in place, no warning before they pulled the trigger,” he says now, 50 years later, sitting on his terrace just outside Pointe-a-Pitre. “They shot me from behind. In the right leg. I say the right leg because it was intentional. They took my right leg, like they cut the right leg from our enslaved ancestors who tried to run away.” The protest began on May 24, when construction workers in Point-a-Pitre went on strike asking for a wage increase of two percent. By the morning of the 26th, their boss, Georges Brizard, agreed to meet union leaders, and Guadeloupe’s governor, Pierre Bolotte, to discuss the pay rise. The striking workers, joined by high-school students among others, were gathered outside the chamber of commerce, where the meeting was taking place, when a rumour spread through the crowd that Brizard had said “the negroes will come back to work when they’re hungry”. When he left the building, escorted by the CRS (French riot police), the protesters vented their anger. Just a few minutes later, orders were given for the police to shoot at “anyone moving”. Racial tensions A former slave colony, the Caribbean islands making up Guadeloupe had become an overseas department of France, which it still is, just 20 years earlier. In 1967, racial inequality was still rife: the white minority held on to most economic, and often political, power while the black majority laboured in sugarcane fields, or, increasingly, in factories and on building sites. Solange Coudrieux, right, was one of many Guadeloupeans to be shot by French police on May 26, 1967. Fifty years on, he and his wife Josselyne, among many others in Guadeloupe, are still waiting for France to officially acknowledge the government’s role in the brutality that took place [Finbar Anderson/Al Jazeera] “Back then, Pointe-a-Pitre was divided in two,” says Jacques Jarvis, who is in his late 60s. “On one side of the boulevard, there were the wealthy whites and on the other, a shanty town full of black workers, living in shacks with tin roofs.” Pointing his finger sternly he adds, “don’t forget there was no state help then. It wasn’t like it is today.” Tensions between the French state and the people of Guadeloupe had boiled over before. During a sugar-worker strike in Le Moule in 1952, police fired on protesters. Ken Kelly, a member of the Guadeloupean independence movement who was a 12-year-old boy at the time, remembers standing in his backyard in the town centre hearing bullets whistle past his head. “I was terrified,” he says. In the run-up to May 1967, relations were particularly strained. In March, protests broke out in Guadeloupe’s former capital, Basse-Terre, following a racist incident involving an old black cobbler and a white shopkeeper. Vladimir Snrsky, a European immigrant, reportedly set his dog on Raphael Balzinc, the cobbler, who was sitting outside Snrsky’s shoe shop. Although reports suggest the dog did not attack Balzinc, who was disabled, Snrsky was heard encouraging the dog: “Say hello to the Negro.” Passersby were drawn to the scene, and the incident evolved into a riot. Snrsky hid on his balcony and was later rescued by police, while angry protesters pushed both his and his wife’s cars into the sea. Fred Demetrius, who was a child at the time, remembers his older brother rushing in and out of their Basse-Terre home “full of excitement”. Fifty years later, standing just a few streets away from where the incident took place, Demetrius recalls how his brother, among others, broke into the shoe shop “not for money”, but because they were so angry. “They didn’t steal anything. They took all the notes from the cash register and tore them up,” Demetrius says. Following the unrest in Basse-Terre, Pierre Bolotte, who had earned himself a fearful reputation during Algeria’s War of Independence, showed similar severity in Guadeloupe when he called in reinforcements from mainland France. He decided then he was going to “rid Guadeloupe of communists and independentists by force,” Kelly says. “He was just waiting for the opportunity.” ‘It wasn’t an ordinary bullet’ ALSO READ: French Algerians return to parents’ native land “I was neither communist nor revolutionary,” says Coudrieux, clutching his stump. “I was a sports teacher.” I saw my leg torn to pieces. There was no curfew in place, no warning before they shot, nothing. Solange Coudrieux, victim of the May 1967 police crackdown Coudrieux was acting as an examiner in another school on the morning of the 26th. On his way home, he picked up his wife and stopped in Pointe-a-Pitre to collect a present for his mother. “The shops were all closed. It annoyed me a bit even. I was told there was a strike, brought about by the construction workers. I went and dropped my wife at her parents before going once more around the town on foot to find a shop that was open.” “When I came to the Place de la Victoire there was a large crowd. Strikes were normal back then, but this was out of the ordinary. There were so many people, running everywhere. They told me the army had shot at the crowd, but me, I fought in the war in Algeria with the French army: I couldn’t believe the army would just shoot at people like that.” One of the first people to be shot and killed that day was Jacques Nestor, who was believed to be a member of GONG, a clandestine movement for Guadeloupean independence. News of his death brought yet more young Guadeloupians out onto the streets in anger. Coudrieux says he later discovered the French police, backed up by the army, had been told to put Pointe-a-Pitre “in a state of war”. By 6pm that day, though, Coudrieux thought it was over. “Calm is restored in Pointe-a-Pitre,” he says they announced on the radio. “But this was a trap.” Fred Demetrius was a child in 1967, but says it’s important that “young people in Guadeloupe realise this is our history” [Finbar Anderson/Al Jazeera] Believing it was safe, Coudrieux set out to walk to the town hall to ask what route he could take to get back to his home in another town. “I saw two cars burning in the street, and next to them I remember passing a man. By the time I could see the town hall, I realised there was no one there so I turned around.” Walking back, though, Coudrieux came across a group of police officers. “I thought they must be returning to the station, so I continued,” he says. “That’s when I heard the first gunshot.” He would later learn that that bullet hit and killed the man he had seen moments before. “A few seconds later, I heard a second gunshot,” Coudrieux says miming a gun being fired. “I felt myself lift up and then fall to the ground. I saw my leg torn to pieces. There was no curfew in place, no warning before they shot, nothing.” “I held my leg, in agony, and played dead. I kept thinking If I move or cry out they’ll certainly shoot me.” Coudrieux says he recalled his French military training: “I could feel my heart pounding and so I tried to control my breathing.” “Once they’d left, I started to shout to the people I could see at the end of the street ‘come and get me, don’t let me die’.” But the people watching him were too scared. “They had seen too many people injured or killed by the armed forces to risk coming to help me,” he explains with a shrug. “Eventually, I managed to drag myself into the shadows. At that moment, a man arrived and took me in his arms. I didn’t know who that man was. But he saved me.” His wife, Josselyne, was waiting at the hospital by the time he arrived. She still recalls the incident with emotion: “The ambulance driver was shaking with fear, he told me they were shooting at him even, shooting at an ambulance!” Two days later, her husband had his leg amputated above the knee. “It wasn’t just an ordinary bullet, you see,” she explains, “it was a dum-dum” which is a type of bullet designed to expand on impact, shattering whatever it hits. “These are banned by The Hague Convention; they’re not allowed in any war, but France used them on its own citizens.” ALSO READ – Q&A: ‘Algeria learned the lesson through bloodshed’ ‘This was our revolution’ Jarvis, who was 18 years old and working as a courier at the time, was delivering documents when he heard the French police were shooting at the crowds. Pointe-a-Pitre became like a war zone ... I remember hearing gunshot after gunshot Jacques Jarvis, victim of police brutality “‘They’ve killed Jacques Nestor, they’ve killed Jacques Nestor,’ that’s what everyone was saying,” he says animatedly, before pausing for a moment to sip his coffee. Looking around the cafe we’re sitting in, he adds in a lower voice, “I’m certain [the French state] targeted him. He was a member of GONG.” On returning to the office, his boss let everyone leave early and instructed them to go to their homes. Jacques, however, headed to the Place de la Victoire. There, he found young men and boys building pyramids of conch shells to throw at the police. “Those were their weapons,” he sighs, “shells, shells against bullets.” “Pointe-a-Pitre became like a war zone,” Jarvis says, describing how police and soldiers drove through the streets on army jeeps, chasing down anyone they came across. “I remember hearing gunshot after gunshot.” At one point, after dark had set in, he ran into a group of police officers. “I tried to get away, I ended up running into the cemetery,” he says, tracing his route with his finger on the table in front of him. “Fate was on my side that day. There was a dug-out grave that ought to have been filled but it was left open. I fell inside it.” “I didn’t understand at first that I’d been shot. I thought that I had broken my arm falling into the grave. But then I realised it was a bullet.” The bullet hadn’t penetrated his arm, but ricocheted off the bone. “I could hear the voices of the police officers, not Guadeloupean voices, but mainland French. They were saying ‘Where is he? Where has he gone?’ “I wasn’t afraid though,” Jarvis adds proudly, “I was thinking about Che Guevara, about Fidel Castro … this was our revolution. I was happy to be there.” He eventually escaped from the cemetery but didn’t return home. “I couldn’t,” he exclaims, raising his arms in exasperation, “I couldn’t turn up at my mother’s house looking like that, covered in mud and blood.” In the street, he came across a man who had been shot. “He was crying out ‘take me home, take me home’ but I didn’t know where his home was,” Jarvis says. “I dragged him to the hospital, instead. But when we arrived, they told me he was already dead.” At the hospital, a nurse cleaned Jarvis up and gave him fresh clothes. “I waited until morning to go home, though,” he says. “The shots from the police’s guns went off throughout the whole night.” ALSO READ – Rokhaya Diallo: ‘France sees itself as a white country’ ‘We will keep pushing for justice’ Reinforcements from the army and the police forces were parachuted into Pointe-a-Pitre that night. The following day saw more protests as others descended on the city to rally against police oppression. There were mass arrests, the French state using the protest and ensuing violence as a pretext to launch a wide-scale crackdown. Upon his release from prison in 1968, Ken Kelly returned to Guadeloupe where he continues to fight for independence [Finbar Anderson/Al Jazeera] Kelly, who was a member of GONG, was in Paris in May 1967. Now, sitting in his living room just outside the capital, he seems almost cheerful as he describes the moment the police came knocking on his door. “It was July 1967, I was arrested for crimes against the state,” he laughs. “Prison was not so bad, though. All the political prisoners were put together.” He adds nostalgically, “we went on hunger strike at one point”. The trial lasted until March 1968, but the state was unable to prove GONG was responsible for the events of May 1967 and Kelly, along with the rest of his GONG comrades, was released. Shortly afterwards, he returned to Guadeloupe, where today he continues to fight for independence. Unlike Kelly, Coudrieux wasn’t interested in politics before 1967. “I certainly didn’t think about independence,” he says. But May 1967 changed that. “France betrayed me,” he exclaims bitterly, clenching his fist. “Since then, I have not considered myself French.” Coudrieux says “of course” he felt the racism in Guadeloupe before May 1967 but it was only as a result of it that he realised “as blacks, we really are considered second-class citizens.” In particular, the events of that May made him deeply mistrustful of the police – as they did many Guadeloupeans. For years afterwards, few people in Guadeloupe who witnessed what had happened dared to speak of it. “No one trusted the police. Particularly my parents’ generation were terrified of repercussions,” Jarvis says. “My mother destroyed all the evidence that I had been involved even.” Some 50 years later, this is changing – slowly. Of the diminishing number of survivors, many are still reluctant to discuss their experience, and many Guadeloupians still distrust the French state and the police in particular. Nonetheless, there are growing efforts to raise awareness about the events of May 1967. “Me 67” (as it is called in Creole) was the theme of this year’s carnival parades across the island. Akiyo and Voukoum, two Guadeloupean cultural organisations, also held events commemorating May 1967 last month. “It is important young people in Guadeloupe realise this is our history,” says Fred Demetrius, a leading member of Voukoum. Waiting for acknowledgment On the cusp of his 80th birthday, Coudrieux, like many others in Guadeloupe, is still waiting for France to officially acknowledge the government’s role in the brutality, including the numbers killed by police fire: while the official record holds that seven were killed, most other estimates put the figure at closer to 100. Grace Carrington, a post-colonial researcher at the London School of Economics who specialises in Guadeloupe, says that there has been no official government apology or acknowledgement. An independent enquiry set up in 2014 by the Ministre des Outre-mer (the overseas ministry), investigated the events of 1967 and last year concluded that due to the lack of evidence, it was impossible to ascertain the number of people who died, Carrington said over email. “Crucially, the report acknowledged the events of May 67 as ‘a massacre during a demonstration, knowingly ordered on the ground, and approved by the government under the presidency of General de Gaulle’,” she said. The events of 1967 are linked to the Algerian War and many colonial structures, such as the police institutions that were present in Algeria were likewise installed in Guadeloupe, according to Carrington. “Many Guadeloupeans were called up to fight for France in Algeria and were greatly affected by their experiences,” she said. During the crackdown, “according to eyewitness accounts, the attitudes of law enforcement officers and those in positions of authority were similar to colonial attitudes towards Algerians prevalent during the Algerian War.” “Unfortunately,” says Carrington, the intelligence police reports from 1967, initially classified for 50 years, that “could have given us a greater understanding”, were mandated – on the eve of the half century anniversary of the brutality – to remain closed for another 25 years. “Many activists and historians have called for these archives to be opened to allow a full understanding of government involvement in the events,” she said. For Coudrieux and others, however, distrust in the state prevails. “The true witnesses are dead, and they [the state] have already made the papers, the evidence, disappear,” Coudrieux says solemnly. “But we will keep pushing for justice. Always.”
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The effectiveness of media promotions and corresponding advertising rates were strongly influenced by the size and scope of the potential audience which could be reached by that format. With regard to outdoor billboard advertising, it had been extremely difficult within the industry to sample or otherwise predict prospective viewer response since there was no way of quantitatively measuring when an advertising display was observed and the frequency of such observations. A further difficulty in accumulating such data resulted because those outdoor displays were placed along highways having fast-moving vehicular traffic. Prior attempts to collect and record information regarding audience exposure to billboard advertising employed such devices as a pressure sensitive tape placed across the roadway which functioned as a counter and thus indicated traffic flow or density. That system, however, merely provided numerical data relative to the number of vehicles but failed to take into consideration whether the occupants within the vehicles observed the roadside display. Another monitoring arrangement utilized concealed cameras that were mounted behind or in close proximity to the billboard and were aimed at the passing automobiles. A distinct shortcoming of that system was that it was based upon the recording and counting of those occupants within the vehicles that were facing in the direction of the billboard. That concept relied upon head movement toward the display as an indication of viewer observation of the display. It should be apparent that that survey method failed to appreciate that a subject viewer did not necessarily need to turn one's head in order to view the roadside display especially if the billboard was visible at some distance along the highway and conversely head movement in the direction of the billboard was not an absolute indicator that the individual was looking at the billboard. Furthermore, tinted automobile windows and the usual accumulation of dirt severely interfered with the ability to observe the occupants. This was also compounded during nighttime when visibility within the automobile was drastically limited and during hazy weather conditions. Another disadvantage of the previous survey methods was that they could not provide accurate data regarding spectator perception because there was no way of determining when the viewer's line of sight was directed at the advertisement. Although the utilization of radiant energy for monitoring eye movement was shown in U.S. Pat. Nos. 3,379,885 and 3,450,446, those devices were not directed to media survey methods using thermal imagery as in the present invention. Additional U.S. patents which disclosed apparatus relying upon eye reflected light include U.S. Pat. Nos. 4,034,401, 3,986,030 and 3,712,716. It should be noted that those last mentioned devices were not concerned with sensing eye movement from a subject in relative motion.
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Traditional automobile bumpers are commonly welded with the chassis to protect automobiles from shocks caused by accidents and also to protect the drivers from harm. But they have little proper action as a buffer to avoid a strong shock. A bumper equipped with an oil pressure has once been made by some makers to furnish a bumper with some shock absorbing movement. However, as the oil stored in the bumper is finite, the oil pressure can make the bumper move quickly back and forth repeatedly to easily cause a concussion to the driver's brain when a colliding accident should happen to the car. And a concussion of a brain does not occur in case of a collision only. Therefore, this two-stage automobile bumper of the present invention has been devised to supply a kind of improved bumper for cars.
3
3
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For many years, ditch processes have been used to treat wastewater. One of the most successful ditch processes known is the Triple Ditch Process. The Triple Ditch Process is particularly known for its ability to perform controlled removal of nitrogen. This process and system differs from conventional activated sludge nitrification and denitrification processes in that it includes no recycle stream or external clarifier. The Triple Ditch system includes three hydraulically interconnected oxidation ditches that alternatively function as aerobic (oxic), anoxic, or quiescent reactors. The aerobic or oxic reactor performs the nitrification. The anoxic reactor performs denitrification. The quiescent reactor performs clarification. Because the flow direction through the oxidation ditches is periodically reversed, there is no need to provide for internal recycle streams or the pumping of return activated sludge. The major advantage of the Triple Ditch system is that it consistently produces a high quality effluent at a significant lower cost than conventional systems. As noted above, the Triple Ditch Process is effective for nitrogen removal as well as the removal of BOD and suspended solids. However, in many situations it is desirable to remove another nutrient—phosphorus. It is, of course, possible to remove phosphorus from wastewater through either chemical means or biologically. There are many disadvantages to using chemicals, not the least of which is cost. Conventional biological phosphorus removal (BPR) usually entails a series of reactors, an external clarifier, and a pumping system for pumping activated sludge from the external clarifier to the front or initial reactor. See, for example, U.S. RE 32,429, the disclosure of which is expressly incorporated herein. Such conventional wastewater treatment systems require large capital expenditures and are expensive to operate and maintain. In many situations, the cost of a conventional phosphorus removal system is cost prohibited. Therefore, there has been and continues to be a need for a cost effective and efficient biological wastewater treatment system that will remove phosphorus.
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(a) Field of the Invention This invention relates to a new method of building wall construction and more particularly, but not by way of limitation, to a method of forming a structural block or brick wall. (b) Discussion of Prior Art Heretofore, brick and block masonry walls have been built by hand, one brick or block at a time. The wall was erected using hand tools for applying mortar on the sides and on the tops of the bricks or blocks. The mortar was mixed on site. This type of wall construction is labor intensive, it is expensive, it is time consuming, it requires mixing mortar on site and it requires skilled masons for well constructed walls. Also, brick and block walls have been preconstructed by forming walls in forms on a horizontal surface on a job site. When the wall is completed, the wall is hoisted upwardly using heavy equipment into a vertical position and attached to a side of a building. This method of wall construction is also time consuming and expensive when having to use additional equipment for lifting each completed wall into place. The subject invention as described herein eliminates the above mentioned problems related to brick and block wall construction. The new method of wall construction allows unskilled brick layers to build a brick or block wall. The method takes half the time when compared to building brick and block walls using mortar and hand tools thereby greatly reducing the overall cost of building construction.
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In a lab just outside Boston, Tufts University professor and engineer Mike Zimmerman and his team have created what might be the next generation lithium-ion battery that will safely power our phones, cars, and more. The key to the invention is a solid plastic electrolyte, the substance that bridges the gap between the positive and negative electrodes. In most lithium-ion batteries, the electrolyte is a liquid, and that can make them vulnerable to fire or explosion when hit or pierced. Those vulnerabilities were recently on display in the recalled Samsung Galaxy Note 7 phones, where the battery would spontaneously explode or catch fire because a corner of the battery casing was too small, bending one of the electrodes and increasing the risk of short circuits. But Zimmerman’s battery can withstand repeated damage without risking explosion or fire. In fact, it can continue to power devices even after most of it has been chopped away.
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Marine scientists from the University of Queensland have discovered hybridized sharks off Australia´s east coast, leading them to believe that some of these predatory beasts display a tendency to interbreed, challenging long-standing scientific theories regarding shark behavior. This is the first time scientists have confirmed a substantial number of hybrid sharks off Australia´s coast, speculating that it may be an adaptation or reaction to climate change; and scientists now believe it may indicate that other shark and ray species may interbreed in reaction to climate change. “Hybridization could enable the sharks to adapt to environmental change as the smaller Australian black tip currently favors tropical waters in the north while the larger common black tip is more abundant in sub-tropical and temperate waters along the south-eastern Australian coastline,” said researcher Jennifer Ovenden of the University of Queensland in a press release. Ovenden and her colleagues said they had discovered 57 sharks that are a cross between the Australian blacktip shark and the common blacktip shark. Both are genetically distinct species, but are closely related, making it easier for the hybridization to occur. “Wild hybrids are usually hard to find, so detecting hybrids and their offspring is extraordinary,” Ovenden said. “To find 57 hybrids along 2000km [1240 miles] of coastline is unprecedented.” The hybridization was confirmed using DNA measurements. The Fisheries Research and Development Corporation co-funded the research, which identified a mismatch between species identification using mitochondrial DNA sequencing and species identification using morphological characters — mature length, birth length, and number of vertebrae. A nuclear DNA marker was sequenced to confirm the hybridization. Dr. Colin Simpfendorfer of James Cook University´s Fishing and Fisheries Research Center said blacktip sharks were one of the most studied species in tropical Australia. “The results of this research show that we still have a lot to learn about these important ocean predators,” he said. Scientists from The University of Queensland, James Cook University´s Fishing and Fisheries Research Center, the Queensland Department of Employment, Economic Development and Innovation and the New South Wales Department of Primary Industries are further investigating the full extent of the hybrid zone and are attempting to measure hybrid fitness. Jess Morgan, another University of Queensland researcher, said that hybrid species are common in fish because their eggs are fertilized in the water. “Sharks physically mate, which is usually a good way to make sure you don’t hybridize with the wrong species,” he told The Australian newspaper. — On the Net: Comments comments
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1. Field of the Invention The present invention relates to a semiconductor device including an oxide semiconductor film and a method for manufacturing the semiconductor device. Note that the semiconductor device in this specification refers to all devices that can function by utilizing semiconductor characteristics, and electro-optic devices, semiconductor circuits, and electronic appliances are all semiconductor devices. 2. Description of the Related Art In recent years, a market for mobile communications typified by mobile phones and the like has grown rapidly. To meet increasing requirements such as low power consumption, high integration degree, many functions, and high speed in semiconductor integration circuits that are mounted components, improvements in transistor characteristics are needed. As one of indexes denoting transistor characteristics, an S-value is given. An S-value represents the amount of a change in gate voltage which is needed for changing a drain current by one digit under constant drain voltage. As the S-value becomes smaller, the controllability of the drain current is increased. Under the present circumstances, it is difficult to make the S-value less than or equal to 80 mV/dec because of miniaturization of transistors and the like. Attention has also been drawn to a technique by which a transistor is manufactured using an amorphous oxide semiconductor material instead of a silicon-based semiconductor material and is applied to an electronic device or the like. For example, a technique for manufacturing a transistor whose channel layer is formed using an amorphous oxide semiconductor material containing indium (In), gallium (Ga), and zinc (Zn) and having an electron carrier concentration lower than 1018/cm3 is disclosed (see Patent Document 1).
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Chlamydiales, Anaplasma and Bartonella: persistence and immune escape of intracellular bacteria. Intracellular bacteria, such as Chlamydiales, Anaplasma or Bartonella, need to persist inside their host in order to complete their developmental cycle and to infect new hosts. In order to escape from the host immune system, intracellular bacteria have developed diverse mechanisms of persistence, which can directly impact the health of their host.
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wave generator used to produce a narrow pulse, or trigger. Blocking oscillators have many uses, most of which are concerned with the timing of some other circuit. They can be used as frequency dividers or counter circuits and for switching other circuits on and off at specific times."> The BLOCKING OSCILLATOR is a special type of wave generator used to produce a narrow pulse, or trigger. Blocking oscillators have many uses, most of which are concerned with the timing of some other circuit. They can be used as frequency dividers or counter circuits and for switching other circuits on and off at specific times. In a blocking oscillator the pulse width (pw), pulse repetition time (prt), and pulse repetition rate (prr) are all controlled by the size of certain capacitors and resistors and by the operating characteristics of the transformer. The transformer primary determines the duration and shape of the output. Because of their importance in the circuit, transformer action and series RL circuits will be discussed briefly. You may want to review transformer action in NEETS, Module 2, Introduction to Alternating Current and Transformers before going to the next section. Transformer Action Figure 3-31 , view (A), shows a transformer with resistance in both the primary and secondary circuits. If S1 is closed, current will flow through R1 and L1. As the current increases in L1, it induces a voltage into L2 and causes current flow through R2. The voltage induced into L2 depends on the ratio of turns between L1 and L2 as well as the current flow through L1. Figure 3-31A. - RL circuit. The secondary load impedance, R2, affects the primary impedance through reflection from secondary to primary. If the load on the secondary is increased (R2 decreased), the load on the primary is also increased and primary and secondary currents are increased. T1 can be shown as an inductor and R1-R2 as a combined or equivalent series resistance (RE) since T1 has an effective inductance and any change in R1 or R2 will change the current. The equivalent circuit is shown in figure 3-31, view (B). It acts as a series RL circuit and will be discussed in those terms. Figure 3-31B. - RL circuit. Simple Series RL Circuit When S1 is closed in the series RL circuit (view (B) of figure 3-31) L acts as an open at the first instant as source voltage appears across it. As current begins to flow, EL decreases and ER and I increase, all at exponential rates. Figure 3-32, view (A), shows these exponential curves. In a time equal to 5 time constants the resistor voltage and current are maximum and EL is zero. This relationship is shown in the following formula: Figure 3-32A. - Voltage across a coil. If S1 is closed, as shown in figure 3-31, view (B), the current will follow curve 1 as shown in figure 3-32, view (A). The time required for the current to reach maximum depends on the size of L and RE. If RE is small, then the RL circuit has a long time constant. If only a small portion of curve 1 (C to D of view (A)) is used, then the current increase will have maximum change in a given time period. Further, the smaller the time increment the more nearly linear is the current rise. A constant current increase through the coil is a key factor in a blocking oscillator. Blocking Oscillator Applications A basic principle of inductance is that if the increase of current through a coil is linear; that is, the rate of current increase is constant with respect to time, then the induced voltage will be constant. This is true in both the primary and secondary of a transformer. Figure 3-32, view (B), shows the voltage waveform across the coil when the current through it increases at a constant rate. Notice that this waveform is similar in shape to the trigger pulse shown earlier in figure 3-1, view (E). By definition, a blocking oscillator is a special type of oscillator which uses inductive regenerative feedback. The output duration and frequency of such pulses are determined by the characteristics of a transformer and its relationship to the circuit. Figure 3-33 shows a blocking oscillator. This is a simplified form used to illustrate circuit operation. Figure 3-32B. - Voltage across a coil. Figure 3-33. - Blocking oscillator. When power is applied to the circuit, R1 provides forward bias and transistor Q1 conducts. Current flow through Q1 and the primary of T1 induces a voltage in L2. The phasing dots on the transformer indicate a 180-degree phase shift. As the bottom side of L1 is going negative, the bottom side of L2 is going positive. The positive voltage of L2 is coupled to the base of the transistor through C1, and Q1 conducts more. This provides more collector current and more current through L1. This action is regenerative feedback. Very rapidly, sufficient voltage is applied to saturate the base of Q1. Once the base becomes saturated, it loses control over collector current. The circuit now can be compared to a small resistor (Q1) in series with a relatively large inductor (L1), or a series RL circuit. The operation of the circuit to this point has generated a very steep leading edge for the output pulse. Figure 3-34 shows the idealized collector and base waveforms. Once the base of Q1 (figure 3-33) becomes saturated, the current increase in L1 is determined by the time constant of L1 and the total series resistance. From T0 to T1 in figure 3-34 the current increase (not shown) is approximately linear. The voltage across L1 will be a constant value as long as the current increase through L1 is linear. Figure 3-34. - Blocking oscillator idealized waveforms. At time T1, L1 saturates. At this time, there is no further change in magnetic flux and no coupling from L1 to L2. C1, which has charged during time TO to T1, will now discharge through R1 and cut off Q1. This causes collector current to stop, and the voltage across L1 returns to 0. The length of time between T0 and T1 (and T2 to T3 in the next cycle) is the pulse width, which depends mainly on the characteristics of the transformer and the point at which the transformer saturates. A transformer is chosen that will saturate at about 10 percent of the total circuit current. This ensures that the current increase is nearly linear. The transformer controls the pulse width because it controls the slope of collector current increase between points T0 and T1. Since TC = L / R , the greater the L, the longer the TC. The longer the time constant, the slower the rate of current increase. When the rate of current increase is slow, the voltage across L1 is constant for a longer time. This primarily determines the pulse width. From T1 to T2 (figure 3-34), transistor Q1 is held at cutoff by C1 discharging through R1 (figure 3-33). The transistor is now said to be "blocked." As C1 gradually loses its charge, the voltage on the base of Q1 returns to a forward-bias condition. At T2, the voltage on the base has become sufficiently positive to forward bias Q1, and the cycle is repeated.
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Q: What Roman institutions were obsolete by the end of the Republic? Background: Recently I've been reading about the Roman Republic, specifically about its last century of civil war and disorder, and I've noticed that some historians say that the Republic fell because its institutions were prepared to handle only a small territory, not the big empire that the Romans conquered throughout the centuries. The most recent book where I found this line of thought was Mary Beard's SPQR, but I've seen it in other places before. The problem is that when these books talk about the end of the Republic, they in general just list events concerning the Gracchus brothers' fight for redistribution of land, Marius' and Sulla's civil wars, and events concerning the First Triumvirate — they never tackle the issues of obsolete institutions directly. Even the article in The Cambridge Companion to the Roman Republic pertaining to the topic only mentions this obsolescence and says the idea is correct, but doesn't elaborate on it. From these works I've gathered that Roman institutions were obsolete precisely because they permitted the existence of this kind of conflict, but I still don't understand why that's the case, which institutions were obsolete and why. Question: What institutions were so obsolete as to cause the fall of the Republic, and why did they function properly only with a small territory? A: The main institutions were the Senate and the military. The personal wealth and power of the members of the Senate, and the rivalries that ensued, threatened to tear the state apart. The creation, and expansion, of a permanent military force, spread across the empire and with each part loyal its own general, who was appointed by the Senate, added a military wing to those senatorial factions. As the empire grew, so did the status of the senators, who gained most from the profits of war and conquest. This exacerbated rivalries between individuals, who also had more resources available to them. Members of the senatorial class were generally arrogant and unaccountable for their actions. Eventually, this would lead to the First Triumvirate 59-53 BC. The acquisition of an empire required that Rome maintain a permanent military establishment in its provinces to cope with rebellions. These were often loyal to their commanders, rather than to the Senate in Rome, as in the cases of Marius (consul in 106 BC & 104-100 BC) and Sulla (consul in 88 BC, & dictator from 82-79 BC). It is interesting to note that during Sulla's two year term as dictator, he was supposed to have had well over a thousand of his political opponents put to death. This resolved the problem of factions within the senate (discussed above), and Sulla was able to retire from office, eventually dying peacefully in his bed. The legions were increasingly being recruited from the provinces, rather than consisting of men from Rome. Even by the 2nd century BC, many of these provinces were beginning to demand full Roman political status commensurate with their role in maintaining the empire. This would result in the the Social War in 91-88 BC. At the same time, the expansion of citizenship was also substantial in the late Republic. In 129 BC the Roman census recorded some 294,000 (male) citizens. This number jumped to about half-a-million in the census of 84 BC (following the settlement of the Social War). By the time of the census conducted by Augustus in 27 BC, that number had reached 5 million! The senate had debated reforms, but these were too little too late. Sources Brunt, P. A: The Fall of the Roman Republic, Clarendon Press, 1988 Mouritsen, Henrik: Plebs and Politics in the Late Roman Republic, Cambridge University Press, 2001 North, John: Politics and Aristocracy in the Roman Republic, in Classical Philology, Volume 85, Number 4 | Oct., 1990 Pavkovic, Michael: The Army of the Roman Republic, Ashgate, 2006 Shotter, David: The Fall of the Roman Republic, Routledge, 2005 Vanderbroeck, Paul: Popular Leadership and Collective Behavior in the Late Roman Republic, Amsterdam, 1987
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When the term dietary fibre was first coined, over sixty years ago, it only referred to plant cell walls in the diet. Since then, the definition of dietary fibre has changed considerably, and the term now encompasses a wide range of different components, including resistant starches and non-digestible oligosaccharides. As a consequence, a huge "library" of publications on dietary fibres is currently available (e.g., Stephen et al. \[[@B1-ijms-19-03556]\]). These publications include reviews, meta-analyses, epidemiological studies, intervention studies involving humans and animals, as well as experimental studies with in vitro systems. In the current decade, most attention is being given to the key role of dietary fibres in modulating the human gut microbiome and to the study of the related effects on metabolic and mental health, which is an area of immense complexity. Contemporary research indicates that the risk of developing various non-communicable diseases is partly mediated by the structure of the gut microbiota maintained by our dietary habits. Ancestral diets, rich in plant-based foods, and dietary fibres appear to favour ecological diversity, with a richer, more complex microbiome resulting in beneficial effects for metabolic and mental health. This field is very much at its beginning stages, and many well-designed studies involving advanced analysis of the complex data generated will be required before an overall picture can emerge. This Special Issue contributes to this major goal, both with review articles and with articles describing new research. The review by Barbara Williams et al. \[[@B2-ijms-19-03556]\] provides strong indications that the more complex and varied the diet is (and its ingredients), the more complex and varied the gut microbiota is likely to be, and concludes that the intake of a complex mix of plant-based foods is to be preferred over the consumption of purified dietary fibres. This conclusion is supported by the results of the study of Samsu U. Nurdin et al. \[[@B3-ijms-19-03556]\]. Here, epigallocatechin-3-gallate (EGCG), the main anti-oxidant of green cincau, combined with its main dietary fibre, pectin, inhibited the ability of pectin to stimulate short-chain fatty acid production in digesta and increased cell proliferation in the distal colon. However, leaves and extracts of green cincau containing these compounds, together with many others, did not show any negative effects. As outlined in the review by O'Keefe (2016) \[[@B4-ijms-19-03556]\], a dietary fibre intake of at least 50 g/day, as consumed in ancestral and non-western diets, contributes to a beneficial gut microbiome and is recommended for a substantial reduction in the risk of colorectal cancer. Suggesting effective dietary fibres as part of a diet may contribute to more detailed dietary recommendations for reducing this risk. The paper by Tahir Rasool Qamar et al. \[[@B5-ijms-19-03556]\] concludes that galacto-oligosaccharides with β-1,6 and β-1,3 glycosidic linkages have dose-dependent protective effects on various biomarkers of colorectal cancer and are more protective in higher doses. This indicates that the addition of these partially synthesized, prebiotic dietary fibres can provide protective effects. The review by Li Pan et al. \[[@B6-ijms-19-03556]\] indicates that a range of prebiotic dietary fibres can protect against a range of negative effects produced by the lectin soybean agglutinin, including effects on the intestinal structure, intestinal permeability, mucosal immune system, and intestinal flora. The authors indicate that functional, prebiotic oligosaccharides can bind to soybean agglutinin, thereby mitigating the negative effects of agglutinin in soybean-containing diets for monogastric animals. The review of Abdallah Ghonimy et al. \[[@B7-ijms-19-03556]\] addresses the important role of carnitine as a factor involved in the production of short-chain fatty acids by bacteria and the interactions between carnitine and dietary fibres, especially those with iron-binding properties, such as lignin and uronic acid-containing polysaccharides. A low dietary fibre intake can stimulate the breakdown of carnitine resulting in the production of compounds that increase the risk of atherosclerosis and cardiovascular disease. Further investigation is required to evaluate the effects of different anti-nutritional factors on carnitine bioactivity. In their study, Sophie Fehlbaum et al. \[[@B8-ijms-19-03556]\] used an in vitro fermentation screening platform (i-screen) inoculated with adult fecal microbiota and exposed it to a range of different dietary fibres. They indicated that the concept of prebiotics has now been considerably broadened beyond the initial concept of non-digestible oligosaccharides and their impact on bifidobacteria and lactobacilli. Their findings support the potential for α-galactooligosaccharides, xyloologosaccharides, and oat β-glucan acting as novel prebiotics, because they caused positive shifts in microbiome composition and short-chain fatty acid production that point to potential health benefits. Finally, another elegant in vitro study was described by Susanne Naumann et al. \[[@B9-ijms-19-03556]\]. They investigated the interaction of dietary fibres with bile acids using simulated in vitro conditions. They compared a commonly used centrifugation method and a modified dialysis method using dietary fibre-rich materials from different sources and concluded that the dialysis method could be used to understand the influence of viscosity on bile acid release from dietary fibres. This may be due to entrapment of bile acids in the viscous chyme matrix in the in vitro conditions used. Further studies on dietary fibre structure and the mechanisms responsible for the viscous effects are required to understand the formation of entangled networks responsible for the entrapment of the bile acids.
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Motor sports enthusiasts and participants in motor racing often have interest in knowing the power output of an engine that operates the motor vehicle. To achieve higher performance, modifications to the motor vehicle and particularly to engines can be made. These modifications include using high performance spark plugs, spark plug wires, superchargers, and with computerized engines replacement computer modules that are “tuned” to enhance performance or that allow “tuning” to the operating characteristics of the particular engine of interest. There are various mechanisms for determining power output of an engine. A chassis dynameter involves a static test of the motor vehicle. The motor vehicle is secured with ties to restrain the motor vehicle from moving and the drive wheels are positioned on rollers. As the engine operates across its RPM (revolutions per minute) range, monitoring equipment measures the loading on the rollers and determines the power output of the engine. This type of test provides a reasonable estimate of the power output under loading. Another test device requires removal of the engine from the motor vehicle and mounting to a test frame. The engine is operated and measurements taken to evaluate performance across the RPM range. While these tests provide a basis for evaluating engine performance and particularly for evaluating the effect of changes to the engine on performance, there are limitations for these tests. Particularly, the tests are static—that is, the motor vehicle is not experiencing real time operating stresses and loads incurred during a road race or vehicle movement. Other mechanical components of the motor vehicle affect engine performance. For example, tire conditions, such as tread, temperature, and air pressure, can affect engine performance. Monitoring the performance of an engine can provide an indication of tire slippage during racing and thus an indication of need to pit and change tires. However, apparatus for the real-time testing of engine performance during motor vehicle moving operation has not been satisfactory for other than professional or serious enthusiasts due to costs and installation needs. Accordingly, there is a need in the art for an improved apparatus and method for real-time measuring and reporting of torque and power of motor vehicles. It is to such that the present invention is directed.
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Saintonge War The Saintonge War was a feudal dynastic encounter that occurred in 1242 and 1243 between forces of Alphonse, Count of Poitiers, supported by Louis IX of France, and those of Hugh X of Lusignan and Raymond VII of Toulouse, backed by Henry III of England, who hoped to regain the Angevin possessions lost three decades prior. Saintonge is the region around Saintes in the centre-west of France in which most of the war occurred. The conflict arose because vassals of Louis in Poitou were displeased with the accession of his brother, Alphonse, as Count of Poitou. The French decisively defeated the English and rebel forces at the Battle of Taillebourg and concluded the struggle at the Siege of Saintes. Louis further repressed the Toulousians into surrendering. He restored Guyenne to Henry as a noble gesture and to seek for further peace so that he could go on a crusade. The battle was the last major conflict between the English and French until the Anglo-French war of 1294-1303. The war announced the end of Henry's hopes of restoring the Angevin Empire lost under King John I of England and further planted the seeds for the Second Barons' war in England, due to the waste of funds and to the growing resentment among the barons towards the king, for his tyrannical ways (by ignoring the Magna Carta) and for his incompetence in war. A feudal revolt The origin of this episode of the predecessor to the Hundred Years War, fought between France and England, was in the revolt of a Poitevin baron, Hugh X, lord of Lusignan. The source of this conflict originated from the confiscation by king Philip Augustus of lands held by king John in France, specifically in Poitiers. Although Richard Earl of Cornwall, John's second oldest son and brother to Henry III, was count of Poitiers after John's death, this was only nominal. King Louis VIII, of France, son of Philip Augustus, had instead transferred the title to his second oldest son, Alphonse de Poitiers. Alphonse was not allowed to take possession of his fiefdom until the age of 18 years, which he did in 1240. In June 1241, king Louis IX of France, son of Louis VIII, held a plenary court at Saumur in Anjou and announced that his brother, Alphonse, having come of age, was ready to come into possession of the title. On that occasion, Alphonse received the homage of the lords of the province, given even by the most powerful of them, Hugh X of Lusignan. Hugh possessed several lands in Poitou, including his family stronghold in Lusignan, the castle of Montreuil-Bonnin and, above all, the County of Marche. Lusignan had a long tradition of autonomy in the heart of Aquitaine, far from the successive capitals of the kingdoms of France and England. Therefore, the Lusignans were not receptive to Capetian authority in the region. Isabelle of Angoulême, mother to Henry and Richard, and now spouse of Hugh, was particularly frustrated that her son had not officially received the title that he had nominally held. Along with a number of other Poitevin lords, Hugh could not accept the loss of autonomy to the increasingly growing demesne of the Capetian royal family, and thus the Poitevin nobility formed a confederacy against the House of Capet. The starting point for the conflict was at Christmas time in 1241, when Hugh X of Lusignan, no doubt at the instigation of Isabelle, insulted the new Count of Poitiers in his own palace, by refusing allegiance. Raymond VII of Toulouse, Count of Toulouse, sought redress for the Treaty of Paris of 1229 (which ended the Albigensian Crusade), under the terms of which he had lost most of his lands, and thus joined the revolting barons as well, but would not participate in the fighting for a while. The Capetian reaction Immediately, the Capetian family reacted. On 5 January 1242, Count Alphonse of Poitiers called together the Poitevin nobles at Chinon for Easter. The faithful lords, and others less loyal but nonetheless enemies of Lusignan, responded to the appeal. Although his mother Blanche of Castile had coped with baronial uprisings before and carried on the royal affairs since 1226, with the title "baillistre" (protector of the heir in feudal law), Louis IX decided to go to the assistance of his brother and forcibly take control of the County of La Marche. In April 1242, Louis assembled a force at Chinon that some contemporaries estimated at around 50,000. On 9 May, he marched against the castle of Montreuil-Bonnin, the fortress of Lusignan. After having seizing a multitude of rebel castles, he steered towards Saintes. On 20 May 1242, Henry and Richard departed from Portsmouth for Royan and joined the rebelling French nobles, forming an army that may have numbered about 30,000. The two kings exchanged letters, but these resolved nothing. Henry had intentions to regain the past Angevin Empire of his predecessors on the basis that the title of Count of Poitou still belonged to his brother, Richard. This was not the first war that Henry had waged in France either as he had earlier lead an expedition to France in 1230, however, Henry was convinced that Hugh would provide the necessary support to reverse the lacklustre results of the last war. While completing his conquest of lower Poitou, he declared war on Saint Louis on 16 July. On 20 July, the French army arrived at Taillebourg where the inevitable clash took place. Battle of Taillebourg Henry advanced to Tonnay-Charente by mid-July and Louis moved to Saint-Jean-d'Angély, just north of Taillebourg, the armies intending to reach the bridge across the Charente River, located in the commune of Taillebourg. Henry and Hugh positioned their army near the village of Saint-James on the west bank of the river and camped in the neighbouring field, while Louis was welcomed to the fortified chateau of Geoffroy de Rancon, the Lord of Taillebourg. Henry decided to send an advance guard to protect the left bank of the Taillebourg bridge, a move that led to a sharp encounter with some French troops on either 21 or 22 July. Louis decided to follow up this engagement and launched a full offensive with the entire French army. The aggressive French assaults carried the day and the English king fled south to the town of Saintes, along with the revolting barons. A prolonged melee fight ensued north of Saintes, however the English were defeated in a definitive fashion. Louis lost comparatively fewer men than the English army but had to face with an epidemic of dysentery that ravaged his army. This forced Louis and his men to return to Paris by August. Siege of Saintes On 22 or 23 July the French army laid siege to the city of Saintes. Henry realized that Hugh did not have as much support as he may have earlier claimed and withdrew to Bordeaux. Shortly afterwards, the citizens handed over the keys to the city to Louis. The resolution of the revolt in France Recognizing that he was in a hopeless position after the siege of Saintes, Hugh surrendered to Louis on 24 July. The settlement of the feudal revolt was devastating for Hugh. His Poitevin castles were confiscated, rearmed, and sold by Alphonse of Poitiers. He further humiliated himself by coming to Louis crying and kneeling before him with his wife and three sons and asked for forgiveness. His daughter Isabel of Lusignan was married to his enemy Geoffrey of Rancon in 1250, who rebuilt his castle with the dowry. It is only during the retreat of the English and rebel forces that Raymond of Toulouse began his campaign against the king. He was able to capture the cities of Narbonne and Albi within August. Unfortunately for Raymond, Roger IV, Count of Foix and vassal to Raymond, stubbornly resisted his war efforts by making his own war with Raymond and submitting only to the king. This gave Louis time to organize an army and split it into two to retake the captured cities. By 30 November, the war with the king came to an end. The war with Roger would persist until January 1243 and would end in yet another defeat for Raymond. Under subjugation, Raymond was forced to give up the two cities that he took and made a promise to fight the Cathar heresy in return for a pardon from the king in Montargis. Blockade of La Rochelle In a final desperate attempt to prevent a complete takeover of his lands in Aquitaine and Gascony, Henry organized a blockade on the port city of La Rochelle by sea to distract French forces from marching further south. The blockade was largely unsuccessful as the outcome of the war had already been mostly determined. Henry looked further for new allies. In January 1243, Henry sent a letter to Frederick II, Holy Roman Emperor, to whom he had made a request for an alliance earlier, announcing the end of his hopes for retaking his possessions in France. On 12 March, Henry was forced to ask Louis for a five-year truce. France and England make peace A truce was signed at Pons on 1 August. A more lasting peace was concluded at Paris on 4 December 1259 amidst the threat of a second Baron's war in England. Initially, Henry refused to give up the rights the territory of his ancestors in France, however, Louis restored Guyenne to Henry, thinking that this noble gesture would assure him an extended time of peace with England because he was mostly concerned with going on the Seventh Crusade in 1248 and wanted to rally support for the cause within his own realm. By signing the treaty, Louis and Henry put an end to the century-old conflict between Capetians and Plantagenets concerning the lands inherited by Henry II of England conquered by Philip Augustus of France. By this text, Henry III renounced his claims concerning Normandy, Anjou, Touraine, Maine, and Poitou; in return Louis IX gave him the necessary sum to maintain 500 knights for two years, plus the revenues of the Agenais, and his domains in the dioceses of Limoges, Cahors and Périgueux. On February 10, 1259, the treaty was first ratified by Richard of Cornwall. On February 17, it was ratified in Westminster by prosecutors in the name of the king, and, by December 4, Simon V de Montfort and Eleanor of England also ratified the treaty. Finally, Henry arrived in France on December 4, 1259 to pay homage to Louis, thus symbolically ending the rivalry. Afterwards, an unexpected and lively friendship arose between the two kings to the point that, sometime later, Louis offered Henry an elephant which had been given to him by the Sultan of Egypt: He also, as Henry's feudal overlord, ratified a papal bull that annulled the Provisions of Oxford, and declared himself as a firm supporter of the Royal prerogative in England. Historical background note In English history, the ‘Hundred Years’ War’ refers to the 116-year period between 1337 – 1453. In some French accounts, that period of conflict is referred to as the ‘Second Hundred Years’ War’, the first embracing the period of upheaval following the change in the balance of power between the French and English thrones from 1159 to 1259 after Henry II of England married Eleanor of Aquitaine gaining many French territories in the process and achieving territorial superiority over the French Kingdom, until the Treaty of Paris (1259), in which the opposite became true. This period saw many conflicts and battles between the two kingdoms such as the Anglo-French War (1202–1214) or the Battle of Bouvines. Notes References Bataille de Taillebourg Bibliography Category:Wars involving France Category:Wars involving England Category:1242 in Europe Category:1243 in Europe Category:1240s in France Category:Conflicts in 1242 Category:Conflicts in 1243 Category:History of Poitou-Charentes Category:Henry III of England
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Taonga pūoro Taonga pūoro are the traditional musical instruments of the Māori people of New Zealand. The instruments previously fulfilled many functions within Māori society including a call to arms, dawning of the new day, communications with the gods and the planting of crops. They are significant in sacred ritual and also fulfill a story-telling role. Many of the sounds of the instruments and tunes are imitations of the sounds of nature, including the wind, the seas and the natural world of birds and insects. Knowledge of taonga pūoro has been revived over the past thirty years by Hirini Melbourne, Richard Nunns and Brian Flintoff. Cultural placement Classifications Taonga pūoro and their uses and classifications are intimately connected with Māori culture and religious practice. The instruments are all part of the families of the gods, and their classifications are directly related to the gods and the creation story where "The Gods sang the Universe into Existence". The universal building blocks of music, melody (Rangi) and rhythm (Papa) are named for the Sky Father and Earth Mother (Ranginui and Papatuanuku, or Rangi and Papa) from the Māori creation story. Further classifications are derived from their children. The god of the winds is Tawhiri, and from him come the wind instruments. The shell instruments are from Tangaroa, god of the sea, and Tane and his daughters Hine Pu te Hue and Hine Raukatauri govern the other instruments derived from forest and earth materials. Today, sometimes substitute materials are used in the making of the instruments and several instruments fall into more than one family being a combination of materials. Traditional usage The use of these instruments, as part of the toolkit of the tohunga (Maori priests), seemed to be exclusively used as an oral flux between Ira Tangata (man) to Ira Atua (the Divine/Gods) or the temporal and the spiritual, which is why Māori regarded them with awe and respect; they were regarded as tapu (sacred/taboo) items of use from the tohunga. When used for entertainment and for recreation, it was a hidden and private practice. Many of these musical traditions had been lost over time because of spiritual reservations Māori people held towards the instruments, but sensitive researchers and enthusiasts such as Richard Nunns, Hirini Melbourne and Brian Flintoff have done considerable restorative work and provided a wealth of knowledge and information around the sounds, history and stories of these taonga (treasures). Today, taonga pūoro are used more frequently at Māori ceremonies and by New Zealand composers. Instruments Wind instruments Flutes Kōauau The kōauau is a small, ductless and notchless flute, long, open at both ends and having from three to six fingerholes placed along the pipe. Kōauau resemble flutes the world over in tone quality and in the range of sounds that can be produced by directing the breath across the sharp edge of the upper aperture. Māori kōauau players were renowned for the power it gave them over the affections of women (notably illustrated by the story of Tūtānekai, who, by playing his kōauau to cause Hinemoa to swim to him across Lake Rotorua). Kōauau are made of wood or bone. Formerly the bone was of bird bone such as albatross or moa; some instruments were also of human bone and were associated with chiefly status and with the traditional practice of utu. Demonstration of the koauau Nguru The nguru is a small vessel flute in the Helmholtz oscillator class, like an ocarina or xun. It is made of wood, soapstone or bone and shaped like a whale's tooth. Sometimes it is made from a whale's tooth. It is from in length, wide at the blowing end and tapering to the lower where it is slightly turned up. It has two or three fingerholes and an extra hole bored on the underside, near the curved end, through which a cord could be passed so that it could hang round the owner's neck. It is played in the same way as a kōauau and produces a similar pure flute-like sound. The nguru is sometimes classified as a nose flute perhaps because the word nguru means to sigh, moan, or snore. This is unlikely because the large end is too wide for a nostril and, if the curved end were placed in that same position, the flute would lie at an impossible angle for the player to reach the fingerholes. Demonstration of melody on Nguru, following, the Pūrerehua Rehu A long flute with a closed top and a transverse blowing hole and finger holes like a pōrutu. Pūmotomoto A long flute with a notched open top which is the blowing edge and a single finger hole near the end - the instrument was chanted through and was traditionally played over the fontanelle of an infant to implant songs and tribal information into the child's subconscious. Pūtōrino The pūtōrino is known for its wide range of voices including a male voice (trumpet) and a female voice (flute). The pūtōrino varies in length from and has an uneven bore, swelling out to the centre and diminishing evenly towards the lower end, where the pipe is narrow, and has either a very small opening or none at all. The outer shape is carved from a solid piece of wood, split in half lengthwise, hollowed out like two small waka and then lashed together again with flax cord or similar substitute for binding. At the widest part of the pipe there is an opening shaped like a grotesque mouth. The finest specimens are decorated at both ends with carved figures, and the open mouth is part of a head which is outlined on the flat surface of the pipe. It can be played with bugle technique, with closed lips which are set in vibration by the rapid withdrawal of the tongue. Small variations of pitch can be produced by moving the forefinger over the centre opening. Demonstration of Pūtōrino Pōrutu The pōrutu is a long version of the kōauau, usually measuring from long. The playing quality differs depending on the material it is made from. New Zealand native hardwoods such as mānuka, mataī, or black maire are suitable for a clean resonating effects. Like the pūtorino, it has 2 voices, the male (trumpet) and female (flute). The female voice can produce up to five harmonics depending on the bore. Trumpets Pūkaea The Pūkaea is a traditional Maori trumpet made of wood. There are several differing designs and lengths within the Pūkaea genre. Pūkaea were used to announce relay signals at times of conflict and were also used to announce the rituals associated with the planting of kumara (sweet potato) and other crops. The function of this instrument is to herald spiritual pathways. As a war trumpet they were used in announcing an oncoming war-party and were dedicated to Tumatauenga (god of war). In the announcement of harvest they were dedicated to Rongomatane (God of agriculture, arts and peace). Today they can be heard heralding the visitors onto the marae or at the opening and closing of important ceremonies. Pūtātara The pūtātara is a traditional Maori conch shell trumpet, which had a variety of roles from signaling to ceremonial and ritual use. Demonstration of the Pūtātara Percussion instruments Pahū Pounamu This Maori musical instrument is made of wood and a jade / greenstone gong and was used in the whare purakau (house of learning). Part of it is made of the jaw bone of the upokohue (pilot whale) and the striker is made from akeake, a native hardwood. Whirled instruments Pūrerehua The Pūrerehua can be made of bone, wood or stone, they are blade-like and swing on a long cord producing a loud, deep whirling that can be heard from a distance. A rapid spinning motion will start the music of the Purerehua'a song as it rotates and flutters. Uses vary from luring lizards, summoning rain, communicating and attracting a soul mate. Demonstration of the Pūrerehua Poi awhiowhio This Maori musical instrument was used as a bird lure. It was made by hollowing a gourd, drilling holes on either side and attaching a cord by which it could be swung around the head creating a whistling, chattering voice that attracted birds. Modern usage Taonga pūoro are currently used for their traditional purposes, but also in many genres of music from classical, orchestral, chamber music, through to pop, alternative and in film music. They were used in the musical sound tracks of films such as Once Were Warriors and Whale Rider, and are becoming more widely used in television and film music to produce authentic natural sounds rather than artificially generated sounds. New Zealand composers such as Gillian Whitehead and Martin Lodge have used taonga pūoro extensively in the genre of art music combining the traditional Maori instruments with western instruments. These composers were noted for this work in March 2013 by UK publication, Gramophone. In 2010, British film and orchestral composer, Paul Lewis collaborated with master taonga pūoro composer and performer, Horomona Horo, to produce, Legends of Rotorua, a fifty-minute composition for a wide variety of taonga pūoro, string quartet, harp, flute, storyteller and soprano. Horomona Horo, the protege of the late Dr Hirini Melbourne and Richard Nunns, was the winner of the inaugural Dynasty Heritage Concerto Competition in 2001, using an array of taonga pūoro. He has collaborated with numerous artists such as Moana and the Moahunters (later Moana and the Tribe), the New Zealand String Quartet, Canto Maori, and Irish group, Green Fire Islands, incorporating taonga pūoro into hip-hop, chamber music, pop, and opera. Salmonella Dub, Tiki Taane and Fat Freddy's Drop have all used taonga pūoro on their albums. The University of Waikato Conservatorium of Music has established a programme to study the instruments in a formal academic capacity under composer and director of The New Zealand Music Research Group, Martin Lodge. Richard Nunns was granted an honorary doctorate by the university in recognition of his contribution to New Zealand Music and the revival of taonga pūoro. He is also a research associate at the University of Waikato. References External links Taonga Puoro Instruments and demonstrations of their sounds Museum of New Zealand: Te Papa Tongarewa Video of Te Hekenga-a-Rangi (Excerpt 1). YouTube Video of Te Hekenga-a-Rangi (Excerpt 2). YouTube Song with images of the pūtōrino. YouTube Video about traditional Pūoro part of the Cook Forster collection with Richard Nunns. YouTube Category:Māori musical instruments Category:New Zealand music Category:Sacred musical instruments
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Wireless mobile communication technology uses various standards and protocols to transmit data between a node (e.g., a transmission station) and a wireless device (e.g., a mobile device). Some wireless devices communicate using orthogonal frequency-division multiple access (OFDMA) in a downlink (DL) transmission and single carrier frequency division multiple access (SC-FDMA) in an uplink (UL) transmission. Standards and protocols that use orthogonal frequency-division multiplexing (OFDM) for signal transmission include the third generation partnership project (3GPP) long term evolution (LTE), the Institute of Electrical and Electronics Engineers (IEEE) 802.16 standard (e.g., 802.16e, 802.16m), which is commonly known to industry groups as WiMAX (Worldwide interoperability for Microwave Access), and the IEEE 802.11 standard, which is commonly known to industry groups as WiFi. In 3GPP radio access network (RAN) LTE systems, the node can be a combination of Evolved Universal Terrestrial Radio Access Network (E-UTRAN) Node Bs (also commonly denoted as evolved Node Bs, enhanced Node Bs, eNodeBs, or eNBs) and Radio Network Controllers (RNCs), which communicates with the wireless device, known as a user equipment (UE). The downlink (DL) transmission can be a communication from the node (e.g., eNodeB) to the wireless device (e.g., UE), and the uplink (UL) transmission can be a communication from the wireless device to the node. In LTE, data can be transmitted from the UE to the eNodeB via a physical uplink shared channel (PUSCH). The PUSCH can carry scheduled data traffic and possible control signaling. The PUSCH can be carried in subframes of a radio frame. A one millisecond (ms) subframe can allow a one ms scheduling interval (or transmission time interval (TTI)). Uplink coverage may be limited by a maximum transmission power of the wireless device. In some situations, a voice-over-internet protocol (VoIP) packet, for example, cannot be transmitted in a one ms subframe with an acceptable error rate. One solution to transmit a VoIP packet is to segment the VoIP packet at higher layers to allow the VoIP packet to be transmitted over several subframes. However, such segmentation can result in additional signaling overhead for each segment (including resource allocation signaling and hybrid automatic repeat request (hybrid ARQ or HARQ) acknowledgement signaling). A technique for improving uplink VoIP coverage at a cell edge can be to use TTI bundling, where a single transport block (TB) from a medium access control (MAC) layer is transmitted in multiple consecutive subframes, with one set of signaling messages (e.g., HARQ acknowledgement feedback) for the whole uplink transmission. For example, the PUSCH can allow groups of 4 TTIs to be bundled together in addition to the single one ms TTI. Reference will now be made to the exemplary embodiments illustrated, and specific language will be used herein to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended.
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Culvert pipes, which are widely used to allow water to flow beneath roads without having to redirect it or construct a bridge to pass over the water, present an ideal place for beavers to construct a dam and restrict the flow of water. A number of previous patents have sought to deal with this problem, in which they prevent beavers from entering culvert pipes by physically obstructing an entrance at an end of the culvert pipe through the use of screens. In addition to deterring beavers from entering culvert pipes, it is important to deter them from building dams that obstruct the flow of water through the culvert pipe, too. For example, U.S. Pat. Nos. 5,102,537; 6,447,206; and 7,441,989 describe cone-shaped screens that block beavers and similarly-sized animals from entering the culvert pipe. Furthermore, the cone-shaped screens deter beavers from constructing dams as the beavers are unable to properly anchor the dam. In spite of these benefits, screen-based beaver control devices have shortcomings. Firstly, the small debris may still gather at the screen and promote clogging of the entrance of the culvert pipe. Furthermore, these screens inhibit passage of fish and turtles through the culvert pipe.
3.453125
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1. Introduction {#sec1-foods-08-00572} =============== The human population is predicted to increase to 9.6 billion by 2050. This population growth combined with an increase in consumer demand for food protein is expected to nearly double the demand for food \[[@B1-foods-08-00572]\]. With more than 1900 species, edible insects represent an interesting source of protein for human consumption \[[@B1-foods-08-00572]\]. Edible insects are widely consumed in many parts of the world and some studies have listed the many advantages of entomophagy compared to conventional livestock production systems. The first is the low environmental impact of edible insect production. Compared to conventional livestock meat, the production of edible insects could reduce land use, water consumption, greenhouse gas emissions, and feed conversion \[[@B1-foods-08-00572]\]. More specifically, and according to a life cycle assessment, Smetana et al. \[[@B2-foods-08-00572]\] demonstrated that the production of edible insect-based protein powder is two to five times more environmentally beneficial than the production of animal products such as poultry and meat. Moreover, Oonincx et al. \[[@B3-foods-08-00572]\] demonstrated that the global warming potential and land uses of edible insect production were lower than for other protein sources. The second advantage is related to their high nutritional value. Edible insects are a good source of proteins (55.0%--70.7% w/w for *Acheta domesticus* (*A*. *domesticus*) and 47.2%--65.3% w/w for *Tenebrio molitor* (*T. molitor*), lipids (9.8%--22.8% w/w for *A. domesticus* and 14.9%--43.1% for *T. molitor*), minerals (3.6%--9.1% for *A. domesticus* and 2.7%--4.3% for *T. molitor*) and essential fatty acids, such as linoleic and linolenic acids \[[@B4-foods-08-00572],[@B5-foods-08-00572],[@B6-foods-08-00572]\]. However, in Western countries, many cultural and psychological barriers stand in the way of consumer acceptance of insects as food \[[@B1-foods-08-00572],[@B7-foods-08-00572]\]. Nevertheless, to reduce insect food neophobia, previous studies proposed to insert invisible edible insects into various food preparations \[[@B8-foods-08-00572]\]. This suggests that incorporation of edible insect powder or ingredients into familiar products could increase acceptance and consumption of edible insects \[[@B9-foods-08-00572],[@B10-foods-08-00572]\]. Nevertheless, the production of edible insect ingredients, such as protein concentrates or isolates, is a major challenge for food processing optimization. Indeed, because high lipid content can interfere with protein extraction, it is necessary to include a lipid separation step to enhance protein extraction. Several lipid extraction methods with conventional solvents are described in the literature. Alternative environmentally friendly solvents, such as methanol and ethanol, are also recommended \[[@B11-foods-08-00572]\]. Three-phase partitioning (TPP) was first reported to be an efficient method for protein extraction, but it is also a good strategy for extracting oil from oleaginous material such as soybeans, seed kernels or almonds, apricots, and rice bran \[[@B12-foods-08-00572]\]. Finally, supercritical CO~2~ (SC-CO~2~) extraction is another common oil extraction method known for its low operating cost and environmental impact \[[@B13-foods-08-00572]\]. Several studies have focused on lipid extraction methods applied to insects. Most were performed on wild-caught edible insects using organic solvents for lipid extraction. For example, Tzompa-Sosa et al. \[[@B5-foods-08-00572]\] extracted lipid fractions from four insect species (*T. molitor*, *Alphitobius diaperinus*, *A. domesticus*, and *Blaptica dubia*) using Soxhlet, aqueous, and Folch extraction methods. Aqueous extraction of lipid gave the lowest lipid yield for all edible insect types, whereas Soxhlet and Folch produced similar yields. Using *T. molitor*, Zhao et al. \[[@B13-foods-08-00572]\] obtained similar defatting efficiencies (lipid extraction yield of about 30%) using ethanol or a mixture of hexane and isopropanol. The application of supercritical CO~2~ to extractions of *T. molitor* produced a range of defatting from 21% to 95%, depending on duration, temperature, and pressure applied \[[@B14-foods-08-00572]\]. This method has many advantages, such as being solvent free and reducing oxidation of lipid components \[[@B14-foods-08-00572]\]. These previous studies demonstrated that the quality of the lipid extract is greatly affected by the extraction procedure. Consequently, the lipid extraction method must be carefully chosen. In this context, the aims of the present study are to investigate the impact of the six conventional and alternative defatting methods on 1) the lipid extraction yield and lipid profile recovered, and 2) the protein extraction and purification rates. 2. Materials and Methods {#sec2-foods-08-00572} ======================== 2.1. Insects {#sec2dot1-foods-08-00572} ------------ House cricket (*A. domesticus*) and mealworm (*T. molitor*) meals were provided by Entomo Farm (Norwood, Ontario, Canada). The global composition of these two edible insects is presented in [Table 1](#foods-08-00572-t001){ref-type="table"}. The protein content was determined according to the Dumas method \[[@B8-foods-08-00572],[@B15-foods-08-00572]\] (Elementar rapid Micro N cube, Langenselbold, Germany), using a conversion factor of 4.76 to convert nitrogen content to protein content, as determined by Janssen et al. \[[@B16-foods-08-00572]\] for whole insect meal. The ash content was determined by an incineration method (AOAC 938.08) \[[@B17-foods-08-00572]\], and the chitin content was determined by the method described by Spinelli et al. \[[@B18-foods-08-00572]\]. 2.2. Lipid Extraction Methods {#sec2dot2-foods-08-00572} ----------------------------- [Figure 1](#foods-08-00572-f001){ref-type="fig"} shows the established protocol described in the following sections. Briefly, *A. domesticus* and *T. molitor* meals were defatted, in triplicate, using one of six different methods. The resulting oils and defatted fractions were recovered and weighed. Between extraction and analysis, these were kept at −20 °C. Oil samples were kept under a nitrogen atmosphere. ### 2.2.1. Soxhlet Method {#sec2dot2dot1-foods-08-00572} Ten grams of insect meal was deposited in a cellulose cartridge (Fisher Scientific catalog number 12-101-100) and the lipids were extracted for 6 h using a Soxhlet apparatus, as described by Tzompa-Sosa et al. \[[@B5-foods-08-00572]\]. Four different solvents, hexane, petroleum ether, ethyl acetate, and 95% ethanol, were used for the extractions. After each extraction, the solvent was completely removed using a rotary evaporator (R-215, Büchi, Flawil, Switzerland). The lipid extracts and the defatted insect meals were dried at 50 °C in a vacuum oven for a minimum of 5 h and were kept in a desiccator at room temperature before weighing. Lipid extracts were stored at −20 °C. ### 2.2.2. Three-Phase Partitioning Method {#sec2dot2dot2-foods-08-00572} The TPP extraction method applied to insect meals was adapted from Dutta et al. \[[@B12-foods-08-00572]\] and Panadare and Rathod \[[@B11-foods-08-00572]\]. Briefly, 10 g of insect flour was mixed with 60 mL of distilled water. The pH of the solution was adjusted to 4.5 with 0.1 M HCl. Next, 20 g of ammonium sulfate and 60 mL of *tert*-butanol (*t*-butanol) were added and the mixture was stirred at 35 °C for 1 h. The mixture was kept at room temperature for 1 h without agitation and centrifuged at 2800× *g* for 5 min. Supernatants were collected in a pre-weighed round-bottom flask and the *t*-butanol was evaporated using a rotary evaporator (R-215, Büchi, Flawil, Switzerland). Extractions were performed in triplicate and oil samples were kept under a nitrogen atmosphere at −20 °C until used. ### 2.2.3. Supercritical Carbon Dioxide {#sec2dot2dot3-foods-08-00572} Supercritical CO~2~ extraction was performed in triplicate at the Centre d'étude des procédés chimiques du Québec (CÉPROCQ) (Montreal, Quebec, Canada) with a laboratory-scale unit, according to the method of Purschke et al. (2017) \[[@B14-foods-08-00572]\]. Equal masses (15 g each) of insect meal and glass marbles were added to a 500 mL reactor operating at a flow rate of 10 g/mL for 75 min (325 bar, 55 °C). Oil and defatted residue were collected after extraction and weighed. The oil fraction was kept at −20 °C under a nitrogen atmosphere until used. 2.3. Characterization of Fatty Acid Methyl Esters (FAMEs) by Gas Chromatography {#sec2dot3-foods-08-00572} ------------------------------------------------------------------------------- Oil fractions were derivatized prior to analysis of FAMEs (fatty acid methyl esters). One drop of extracted oil was introduced into a 10 mL screw cap tube. One mL of hexane was added, followed by 0.5 mL of 0.05 M sodium methanolate. The cap was tightened, and the solution was vortexed before heating in a water bath at 40 °C for 15 min. After heating, 2 mL of hexane and 3 mL of saturated NaCl solution were added. The solution was vortexed again and left at rest until the two phases were separated. The organic phase containing FAMEs was collected (supernatant) and filtered through a glass pipette equipped with 1 cm of anhydrous sodium sulfate. The FAMEs were collected in a clean 10 mL screw cap tube. The aqueous phase was washed twice with an additional 2 mL of hexane. The supernatant was collected after phase separation, filtered in a glass pipette as above, and added to the previous 10 mL tube. Another 5 mL of hexane was added for a final hexane volume of 10 mL, and a FAME concentration of about 1 mg/mL. One microliter of the FAME solution was injected onto a GC-2010 Plus Gas Chromatograph (Shimadzu, Kyoto, Japan) equipped with a BPX70 column (60 m × 0.25 mm internal diameter × 0.25 µm film thickness; SGE, Melbourne, Australia) and a flame ionization detector (FID). Dihydrogen (H~2~), at a flow rate of 1.29 mL/min, was the carrier gas. The injector (split ratio 50:1) was maintained at 250 °C with a purge flow of 3 mL/min. The temperature started at 60 °C for 1 min, increased to 190 °C at 5 °C/min, was maintained at 190 °C for 15 min, then finally increased to 240 °C at 5 °C/min where it was maintained for 1 min, for a total program time of 53 min. The FAMEs were identified by comparing the retention time of the peaks with a commercial standard (C4 to C22 GLC-607; Nu-Chek Prep, Elysian, MN, USA). Analyses were performed in triplicate and the data were analyzed with GCsolution software, version 2.32.00 (Shimadzu, Kyoto, Japan). 2.4. Protein Extraction {#sec2dot4-foods-08-00572} ----------------------- *A. domesticus* and *T. molitor* proteins were extracted according to Zhao et al. \[[@B13-foods-08-00572]\]. For both insects, 4 g of defatted or regular (control) meal was added to 60 mL of 0.25 M NaOH. The mixture was agitated for 60 min at 40 °C and centrifuged at 3500× *g* for 20 min at 4 °C. The supernatant was removed, and a second extraction was performed on the residue. Supernatants from the first and second alkaline solubilization were pooled and the pH was adjusted to 4.3--4.5 to induce protein precipitation with 2 M HCl before centrifugation (2500× *g*, 15 min, 4 °C). After protein precipitation, the supernatant was removed, and the residue containing precipitated proteins was washed twice with distilled water at pH 4.5 and centrifuged (2500× *g*, 10 min, 4 °C). The residue and the supernatant were freeze-dried. The powders of the two fractions were analyzed using the Dumas combustion method (Elementar rapid Micro N cube, Langenselbold, Germany). A conversion factor of 5.60 was used to convert the nitrogen percentage to protein content of insect protein extract, as determined by Janssen et al. \[[@B16-foods-08-00572]\]. This conversion factor is different than that used to determine the protein content of the whole insect meal ([Table 1](#foods-08-00572-t001){ref-type="table"}), because the non-protein nitrogen (NPN) content is reduced during the protein extraction \[[@B16-foods-08-00572]\]. 2.5. Extraction Yields {#sec2dot5-foods-08-00572} ---------------------- For all lipid extraction methods, the oil extraction yield was calculated according to Equation (1): where m~f~ is the mass of extracted fat (g) and m~i~ is the mass of crude *A. domesticus* and *T. molitor* meal (g). As proposed by Zhao et al. \[[@B14-foods-08-00572]\] for *T. molitor*, the extracted fat was expressed as a percentage the initial mass of edible insect meal samples, which means that the most efficient defatting method could not have a 100% lipid extraction yield. The protein extraction yield was calculated according to Equation (2) \[[@B19-foods-08-00572]\]: where m~r~ represents the mass (g) and %P~r~ represents the protein content (% w/w) of the residue after protein precipitation, and m~d~ and %P~d~ represent the mass (g) and the protein content (% w/w) of defatted *A. domesticus* or *T. molitor* meal (respectively). The protein purity was obtained when determining the nitrogen content of each sample (Elementar rapid Micro N cube, Langenselbold, Germany). 2.6. Statistical Analysis {#sec2dot6-foods-08-00572} ------------------------- Statistical analyses were performed using Statistical Analysis System (SAS) University Edition, SAS^®^ Studio 3.5 software. A randomized complete block design with six treatments (different extraction methods) in multiple blocks (*n* ≥ 3) was used. For each experiment, the experimental unit was *A. domesticus* or *T. molitor* meal, which received one treatment. Each experiment was performed in triplicate and results were reported as mean ± standard deviation (SD). Tukey tests (α = 0.05) were used as multiple comparison tests. Statistical analyses were done independently for *A. domesticus* and *T. molitor*. 3. Results and Discussion {#sec3-foods-08-00572} ========================= 3.1. Lipid Extraction Yield and Fatty Acid Composition {#sec3dot1-foods-08-00572} ------------------------------------------------------ [Table 2](#foods-08-00572-t002){ref-type="table"} shows the fat extracted (% w/w of the insect meal) from both insect meals obtained from the different defatting methods. The extraction yields were higher for *T. molitor* (22.1%--28.8% w/w) compared to *A. domesticus* (11.9%--22.7% w/w). This difference is explained by the fact that crude *T. molitor* has a higher fat content than *A. domesticus* (36% w/w \[[@B20-foods-08-00572]\] vs. 18.6%--22.8% w/w \[[@B21-foods-08-00572]\]). The results showed that the defatting method significantly impacts the lipid extraction yields for *A. domesticus* (*p* \< 0.05), unlike for *T. molitor* (*p* \> 0.05). Significant differences were observed between Soxhlet extractions of *A. domesticus*, depending on the solvent used (*p* \< 0.05). Ethanol produced the highest lipid extraction rate at 22.7% w/w. The lipid extraction rates for TPP and ethyl acetate were similar, and hexane and SC-CO~2~ were the least efficient methods for lipid extraction with values of 14.6% and 11.9%, respectively. Further optimization of the SC-CO~2~ method using co-solvent might improve the extraction yield in a future work, as shown by Rudyk et al. \[[@B22-foods-08-00572]\] for the extraction of nonfood and nonpolar compounds. The fatty acid (FA) profiles of lipids extracted from *A. domesticus* and *T. molitor* meals are shown in [Table 3](#foods-08-00572-t003){ref-type="table"}; [Table 4](#foods-08-00572-t004){ref-type="table"}, respectively. For both insects, the three most abundant FAs were palmitic acid (C16:0), vaccenic acid (C18:1V), and linoleic acid (C18:2). For *A. domesticus*, C18:2, which is an essential fatty acid, represented 29%--36% of the total FA, while C16:0 and C18:1V comprised 26%--31% and 21%--24% of the total FA, respectively. Stearic acid (C18:0) was the fourth most abundant FA of *A. domesticus*, ranging between 10% and 11% of the total FA. For *T. molitor*, C18:1V was the dominant FA at 37%--40% of the total FA. The second most abundant *T. molitor* FA was C18:2 (33%--37%), followed by C16:0 (18%--19%). Except for these major FAs, the remaining FAs found in both edible insect lipid extracts were detected at very low relative abundance. Some differences were observed, especially the abundance of C14:0, C17:0, C17:1, and C18:1V, which were higher in *T. molitor* oil extract, or the abundance of C16:0, C18:0, and C18:1 (oleate), which were higher in *A. domesticus* oil extract. Finally, arachidic (C20:0), transvaccenate (C18:1T), petroselinate (C18:1P), gamma-linolenic (C20:3), and docosahexaenoic (C22:6) acids were detected in *A. domesticus* oil, but were absent from *T. molitor* oil. These results agreed with the work of Tzompa-Sosa et al. \[[@B5-foods-08-00572]\] who reported that C18:1, C18:2, and C16:0 were the three most abundant FA in four insect species, including *T. molitor* and *A. domesticus*. Mariod et al. \[[@B21-foods-08-00572]\] findings also supported these results as they indicated that the major FA of adult *A. domesticus* were C18:2 (30%--40%), C18:1 (23%--27%), C16:0 (24%--30%), and C18:0 (7%--11%). They also reported the occurrence of smaller amounts of palmitoleic (C16:1), myristic (C14:0), and linolenic acids (C18:3). Moreover, the proportions of FA obtained from *T. molitor* larvae with SC-CO~2~ were close to the results obtained by Purschke et al. \[[@B14-foods-08-00572]\], who found 18.46% of C16:0, 2.41% of C18:0, 42.14% of C18:1, and 29.00% of C18:2 for the same treatment (325 bar, 55 °C, 75 min). There were some differences in the FA profiles, depending on the defatting method used. For both edible insects, Soxhlet extraction with ethanol or TPP were the two least efficient methods for extracting C16:0, whereas SC-CO~2~ was the most efficient. For *A. domesticus* only, Soxhlet extraction with hexane or TPP extracted more C18:0. Ethanol was the least efficient solvent, but there was no significant difference between ethanol and petroleum ether, ethyl acetate, or SC-CO~2~. For both insects, SC-CO~2~ extracted the highest proportion of transvaccenic acid, but no significant difference was observed between Soxhlet extractions with hexane or petroleum ether (or ethyl acetate for *T. molitor*, exclusively). Like the C18:0 extractions, ethanol was the least efficient extraction method for transvaccenic acid but there was no significant difference (*p* \> 0.05) between this method and TPP (and ethyl acetate for *A. domesticus* only). Moreover, for both *A. domesticus* and *T. molitor*, TPP and Soxhlet extraction with ethanol were the two defatting methods extracting the most C18:2. With both insects, extraction of the three most abundant FAs showed that ethanol and TPP, two defatting methods using polar solvents (ethanol and *t*-butanol), are more efficient at extracting C18:2, whereas methods using nonpolar solvents are more efficient at extracting C18:1 and C16:0. These results agree with the findings of Murali et al. \[[@B23-foods-08-00572]\]. These authors fractionated lipids from *Fusarium* spp. into polar and nonpolar classes using ethanol (polar) and petroleum ether (nonpolar). They found a higher quantity of C18:2 in the polar lipid fraction, whereas the nonpolar lipid fraction contained more C18:1 \[[@B23-foods-08-00572]\]. The results obtained in this study also agree with the fact that polyunsaturated fatty acids (PUFA) such as C18:2 are relatively more polar than monounsaturated fatty acids (MUFA) such as C18:1V and long-chain saturated FAs such as C16:0 \[[@B24-foods-08-00572]\]. As explained previously, ethanol produced the highest fat extraction yield. However, for FA quantification, its efficiency was highly dependent on FA relative polarity. These results show that lipids other than FA also affect the fat extraction yield. Indeed, phospholipids, the second most important lipid in insects, after triglycerides, are polar components and therefore very easily solubilized in a polar solvent, such as ethanol, methanol \[[@B20-foods-08-00572],[@B25-foods-08-00572]\], or even *t*-butanol, used for TPP extraction. Conversely, triacylglycerols or sterol esters have very low polarity and, so, are soluble in nonpolar solvents, such as hexane and ether \[[@B25-foods-08-00572]\]. It can therefore be hypothesized that all categories of lipids were present in the same proportions for *T. molitor*, leading to the non-significant differences (*p* \> 0.05) in fat extraction yields observed for the defatting methods under study. However, *A. domesticus* meal may have contained a higher proportion of polar lipids since methods using polar solvents such as ethanol and *t*-butanol were significantly more efficient at extracting fat from this insect species. These findings suggest that the most suitable defatting method may differ from one insect to the other, depending on its lipid composition. 3.2. Protein Extraction and Purity {#sec3dot2-foods-08-00572} ---------------------------------- Protein extraction experiments were performed on defatted *A. domesticus* and *T. molitor* to generate an enriched protein fraction. Protein concentrations of initial *A. domesticus* and *T. molitor* meals were 53% and 45% w/w on a dry basis, respectively. According to Rumpold and Schulter \[[@B6-foods-08-00572]\], the protein content of *A. domesticus* meal ranged from 55% to 70%, compared to 47% to 60% for *T. molitor*. These results are higher than those observed in the present study since they used a protein conversion factor of 6.25. However, it was recently suggested by Janssen et al. \[[@B16-foods-08-00572]\] that this conversion factor overestimates protein concentration because it includes natural nitrogen-containing polysaccharides such chitin, or chitosan, or inorganic nitrogen such as uric acid, urea, or ammonia \[[@B26-foods-08-00572]\]. Consequently, a protein conversion factor of 5.60, used in this study, seems more appropriate for evaluating the protein content of the protein extract of whole meal and defatted protein extracts \[[@B16-foods-08-00572]\]. Assuming an overestimation of protein concentration in the literature, the protein concentrations obtained in this study were comparable \[[@B13-foods-08-00572]\]. The protein extraction yields are presented in [Table 5](#foods-08-00572-t005){ref-type="table"}. Extractions performed on defatted *A. domesticus* and *T. molitor* meals were compared to those on the whole meals ([Table 1](#foods-08-00572-t001){ref-type="table"}) without defatting to evaluate the importance of defatting to increase protein extraction and protein purity. Protein extraction was not performed with defatted meals obtained using TPP since ammonium sulfate was used to precipitate the proteins. Ammonium sulfate contains nitrogen, which interferes with the nitrogen analysis to determine protein content. For *A. domesticus*, there was no significant difference (*p* \> 0.05) in protein purity between the extraction made with the most polar solvent, ethanol (78.5% ± 2.0%), and the least, hexane (74.7% ± 0.3%). No significant were observed either for *T. molitor*. Yi et al. \[[@B7-foods-08-00572]\] used aqueous extraction for insect defatting, and after protein extraction of defatted meal following centrifugation, the purity was 50%--61% in the supernatant fraction. The results of this study demonstrated the importance of defatting insect meals and of precipitating proteins after extraction, to obtain protein concentrates with high purity. Finally, insect protein concentrates and isolates were compared with plant-based proteins. The results are presented in [Table 6](#foods-08-00572-t006){ref-type="table"}. The protein extraction yield of insects was quite inferior to vegetal proteins, depending on the extraction method. However, the protein purity of insect extracts can be compared to other protein matrices, but not the whole meal. In fact, the major compositional difference between insect and plant-based matrices is the presence of chitin that has an important structural role in insects \[[@B27-foods-08-00572]\]. However, chitin in insects, as in crustaceans, is found in a complex matrix made of proteins and fat, rather than in its pure form \[[@B27-foods-08-00572],[@B28-foods-08-00572]\]. Consequently, despite the fact that defatting increases the purity of protein extracts, it might be interesting to find a complementary method that would collapse the chitin matrix and, thus, improve protein extraction yields, and the competitiveness of the edible insect industry. 4. Conclusions {#sec4-foods-08-00572} ============== The impact of six different defatting methods on lipid extraction, fatty acid composition, and protein extraction from two insect meals were investigated. Ethanol provided the highest fat extraction rate. However, according to fatty acid profiles obtained by gas chromatography, ethanol was less effective at extracting relatively nonpolar fatty acids. Consequently, the choice of defatting methodology should be made according to the fat composition of the edible insect used. The lipid extraction method impacts protein extraction, as defatting performed with ethanol produced a higher protein purity for *A. domesticus*. Even if eco-friendly alternatives are available (i.e., SC-CO~2~), there must be a compromise between extraction rate of edible insect macromolecules and sustainability of processing steps. The results also showed that defatting and protein precipitation were important for obtaining good yields and purification rates comparable to results found in the literature for pulse proteins. Furthermore, following this study, it would also be appropriate to optimize the SC-CO~2~ process, notably with the use of co-solvent, to assess the functional properties of these high-purity protein concentrates and to validate their incorporation into functional foods. The authors would like to thank Yacine Boumghar and Mathieu Sarrazin from Centre d'étude des procédés chimiques du Québec (CEPROCQ, Quebec, Canada) for SC-CO~2~ extractions, Diane Gagnon and Sophie Fortin (Department of Food Sciences, Université Laval, Quebec, Canada) for their input into this project, and Barb Conway for editing this manuscript. Writing---original draft preparation, investigation, and data curation, M.L. and V.P.; writing---review and editing, V.P., A.M., J.C., A.G., and A.D.; supervision and project administration, A.D.; funding acquisition, A.D. This research was funded by Fonds de Recherche du Québec---Nature et technologies, grant number 2018-PR-208090. The authors declare no conflict of interest. ![General scheme of experimental procedure.](foods-08-00572-g001){#foods-08-00572-f001} foods-08-00572-t001_Table 1 ###### Physicochemical characterization (% w/w on a dry basis) of *Acheta domesticus* (*A. domesticus*) and *Tenebrio molitor (T. molitor)* meals. ------------------------------------------------------------------------------ Insect Meal Protein Ash Chitin Other\ (Sugar, Lipid, etc.) ----------------- ------------- ----------- ----------- ---------------------- *A. domesticus* 53.5 ± 0.3 5.5 ± 0.1 5.9 ± 0.6 35.1 ± 0.6 *T. molitor* 45.7 ± 0.02 4.3 ± 0.1 7.2 ± 0.5 42.9 ± 0.6 ------------------------------------------------------------------------------ foods-08-00572-t002_Table 2 ###### Lipid extraction yield of *A. domesticus* and *T. molitor* meals, according to the defatting method. ----------------------------------------------------------------------- Insect Meal Defatting Method Extracted Fat\ (% w/w of Sample Mass) --------------------------- ------------------ ------------------------ *A. domesticus* Soxhlet (Hexane) 14.6 ± 0.1 ^c^ Soxhlet (Petroleum ether) 14.7 ± 0.2 ^c^ Soxhlet (Ethyl acetate) 15.1 ± 0.3 ^b^ Soxhlet (Ethanol) 22.7 ± 2.9 ^a^ TPP 19.3 ± 2.0 ^ab^ SC-CO~2~ 11.9 ± 1.4 ^c^ *T. molitor* Soxhlet (Hexane) 25.5 ± 0.1 ^a^ Soxhlet (Petroleum ether) 24.3 ± 1.2 ^a^ Soxhlet (Ethyl acetate) 25.7 ± 0.3 ^a^ Soxhlet (Ethanol) 28.8 ± 5.9 ^a^ TPP 23.7 ± 2.4 ^a^ SC-CO~2~ 22.1 ± 0.6 ^a^ ----------------------------------------------------------------------- SC-CO~2~: supercritical CO~2~, TPP: three-phase partitioning. Mean values ± SD with different letters are significantly different (Tukey test, α = 0.05, *n* = 3). foods-08-00572-t003_Table 3 ###### Relative abundance of fatty acid composition from *A. domesticus* oil. Fatty Acid Relative Abundance (u.a.) ------------ --------------------------- -------------------- -------------------- ------------------- -------------------- ------------------- ------------------ Saturated C14:0 0.81 ± 0.03 ^b^ 0.83 ± 0.04 ^b^ 0.81 ± 0.05 ^b^ 0.69 ± 0.03 ^c^ 0.60 ± 0.10 ^c^ 0.95 ± 0.03 ^a^ C16:0 27.70 ± 1.00 ^a,b^ 27.50 ± 0.30 ^a,b^ 26.90 ± 1.10 ^a,b^ 24.60 ± 0.70 ^b^ 25.10 ± 2.40 ^b^ 29.60 ± 0.30 ^a^ C17:0 0.29 ± 0.01 ^a^ 0.25 ± 0.02 ^a^ 0.24 ± 0.03 ^a,b^ 0.21 ± 0.01 ^a,b^ 0.10 ± 0.10 ^b^ 0.22 ± 0.00 ^a,b^ C18:0 10.30 ± 0.20 ^a^ 10.14 ± 0.03 ^a,b^ 10.00 ± 0.30 ^a,b^ 9.60 ± 0.40 ^b^ 10.50 ± 0.10 ^a^ 9.92 ± 0.08 ^a,b^ C20:0 0.60 ± 0.01 ^a^ 0.57 ± 0.03 ^a,b^ 0.57 ± 0.02 ^a,b^ 0.46 ± 0.04 ^c^ 0.43 ± 0.06 ^c^ 0.50 ± 0.02 ^b,c^ MUFA C16:1 1.17 ± 0.01 ^a^ 1.14 ± 0.03 ^a^ 1.12 ± 0.00 ^a,b^ 1.10 ± 0.03 ^a,b^ 1.02 ± 0.08 ^b^ 1.22 ± 0.05 ^a^ C17:1 \- \- \- \- \- \- C18:1T 0.15 ± 0.01 ^a^ 0.15 ± 0.01 ^a^ 0.14 ± 0.01 ^a^ 0.12 ± 0.00 ^b^ 0.12 ± 0.01 ^b^ 0.11 ± 0.00 ^b^ C18:1P 0.20 ± 0.01 ^b,c^ 0.19 ± 0.03 ^b,c^ 0.18 ± 0.02 ^c^ 0.16 ± 0.02 ^c^ 0.40 ± 0.10 ^a,b^ 0.52 ± 0.08 ^a^ C18:1V 21.40 ± 0.70 ^a,b^ 21.10 ± 0.50 ^a,b^ 20.40 ± 0.40 ^b^ 19.50 ± 0.40 ^b^ 20.30 ± 1.30 ^b^ 22.50 ± 0.40 ^a^ C18:1 0.58 ± 0.02 ^a^ 0.54 ± 0.04 ^a,b^ 0.54 ± 0.04 ^a,b^ 0.50 ± 0.01 ^a,b^ 0.47 ± 0.06 ^b^ 0.60 ± 0.02 ^a^ C20:1 \- \- \- \- 0.10 ± 0.00 ^b^ 0.11 ± 0.00 ^a^ PUFA C18:2 30.10 ± 1.10 ^b,c^ 29.50 ± 0.50 ^c^ 29.30 ± 0.30 ^c^ 33.00 ± 0.70 ^a,b^ 33.60 ± 2.20 ^a^ 27.40 ± 0.50 ^c^ C18:3 1.52 ± 0.01 ^a^ 1.48 ± 0.05 ^a,b^ 1.46 ± 0.03 ^a,b^ 1.47 ± 0.05 ^a,b^ 1.39 ± 0.08 ^b^ 1.48 ± 0.03 ^a.b^ C20:3 0.29 ± 0.01 ^b,c^ 0.28 ± 0.02 ^c^ 0.30 ± 0.00 ^b,c^ 0.43 ± 0.04 ^a^ 0.35 ± 0.04 ^b^ 0.15 ± 0.01 ^d^ C22:6 0.14 ± 0.01 ^b^ 0.14 ± 0.01 ^b^ 0.15 ± 0.02 ^b^ 0.15 ± 0.01 ^b^ 0.17 ± 0.01 ^a,b^ 0.19 ± 0.01 ^a^ C18:1P: methyl petroselinate, C18:1T: methyl transvaccenate, C18:1V: methyl vaccinate, MUFA: monounsaturated fatty acid, PUFA: polyunsaturated fatty acid, SA: Soxhlet (ethyl acetate), SC-CO~2~: supercritical CO~2~, SE: Soxhlet (ethanol), SH: Soxhlet (hexane), SP: Soxhlet (petroleum ether), TPP: three-phase partitioning. Mean values in the same line with different letters are significantly different (Tukey test, α = 0.05, *n* = 3). foods-08-00572-t004_Table 4 ###### Relative abundance of fatty acid composition from *T. molitor* oil. Fatty Acid Relative Abundance (u.a.) ------------ --------------------------- -------------------- -------------------- ------------------ -------------------- ------------------ ------------------ Saturated C14:0 1.65 ± 0.05 ^b^ 1.64 ± 0.02 ^b^ 1.60 ± 0.10 ^b^ 1.67 ± 0.00 ^b^ 1.58 ± 0.01 ^b^ 1.72 ± 0.04 ^a^ C16:0 18.74 ± 0.00 ^a,b^ 18.77 ± 0.03 ^a,b^ 18.67 ± 0.05 ^a,b^ 17.78 ± 0.05 ^c^ 18.20 ± 0.40 ^b,c^ 19.10 ± 0.20 ^a^ C17:0 0.42 ± 0.02 ^a^ 0.40 ± 0.02 ^a^ 0.41 ± 0.00 ^a^ 0.41 ± 0.01 ^a^ 0.44 ± 0.01 ^a^ 0.41 ± 0.00 ^a^ C18:0 2.30 ± 0.01^c^ 2.30 ± 0.01 ^c^ 2.33 ± 0.01 ^b,c^ 2.80 ± 0.08 ^a^ 2.62 ± 0.08 ^a,b^ 2.20 ± 0.20 ^c^ MUFA C16:1 0.93 ± 0.00 ^a^ 0.94 ± 0.02 ^a^ 0.96 ± 0.00 ^a^ 0.95 ± 0.05 ^a^ 0.93 ± 0.03 ^a^ 0.97 ± 0.02 ^a^ C17:1 0.13 ± 0.00 ^a^ 0.13 ± 0.01 ^a^ \- \- 0.11 ± 0.00 ^a^ 0.12 ± 0.00 ^a^ C18:1V 39.74 ± 0.00 ^a^ 39.74 ± 0.07 ^a^ 39.70 ± 0.03 ^a^ 36.94 ± 0.02 ^b^ 38.10 ± 0.60 ^b^ 39.80 ± 0.30 ^a^ C18:1 0.31 ± 0.01 ^a^ 0.29 ± 0.00 ^a^ 0.31 ± 0.01 ^a^ 0.30 ± 0.02 ^a^ 0.30 ± 0.01 ^a^ 0.29 ± 0.01 ^a^ PUFA C18:2 33.76 ± 0.06 ^c^ 33.70 ± 0.05 ^c^ 33.80 ± 0.09 ^c^ 37.00 ± 0.10 ^a^ 34.70 ± 0.50 ^b^ 33.40 ± 0.10 ^c^ C18:3 1.25 ± 0.01 ^a^ 1.24 ± 0.01 ^a^ 1.28 ± 0.01 ^a^ 1.30 ± 0.08 ^a^ 1.21 ± 0.02 ^a^ 1.27 ± 0.01 ^a^ C18:1P: methyl petroselinate, C18:1V: methyl vaccinate, MUFA: monounsaturated fatty acid, PUFA: polyunsaturated fatty acid, SA: Soxhlet (ethyl acetate), SC-CO~2~: supercritical CO~2~, SE: Soxhlet (ethanol), SH: Soxhlet (hexane), SP: Soxhlet (petroleum ether), TPP: three-phase partitioning. Mean values in the same line with different letters are significantly different (Tukey test, α = 0.05, *n* = 3). foods-08-00572-t005_Table 5 ###### Mass and protein yield of the residue after protein precipitation of *A. domesticus* and *T. molitor*, according to the defatting method. ---------------------------------------------------------------------------------------------------------- Insect Meal Defatting Method Protein Extraction Yield\ Protein Purity\ (%) (%) --------------------------- -------------------------------- --------------------------- ----------------- *A. domesticus* Whole meal (without defatting) 38.9 ± 1.7 ^a^ 58.3 ± 0.5 ^d^ Soxhlet (Hexane) 32.4 ± 3.8 ^ab^ 74.7 ± 0.3 ^ab^ Soxhlet (Petroleum ether) 33.1 ± 1.0 ^ab^ 74.3 ± 2.0 ^b^ Soxhlet (Ethyl acetate) 31.6 ± 3.0 ^b^ 74.4 ± 1.2 ^b^ Soxhlet (Ethanol) 31.0 ± 4.0 ^b^ 78.5 ± 2.0 ^a^ TPP ND ND SC-CO~2~ 33.7 ± 1.1 ^ab^ 70.1 ± 1.9 ^c^ *T. molitor* Whole meal (without defatting) 39.3 ± 0.8 ^a^ 48.7 ± 0.1 ^b^ Soxhlet (Hexane) 33.7 ± 1.6 ^b^ 74.0 ± 2.2 ^a^ Soxhlet (Petroleum ether) 33.5 ± 1.2 ^b^ 72.7 ± 1.5 ^a^ Soxhlet (Ethyl acetate) 33.2 ± 0.6 ^b^ 75.4 ± 0.5 ^a^ Soxhlet (Ethanol) 33.9 ± 3.7 ^b^ 75.3 ± 0.8 ^a^ TPP ND ND SC-CO~2~ 36.4 ± 1.5 ^ab^ 72.7 ± 4.1 ^a^ ---------------------------------------------------------------------------------------------------------- ND: not determined, SC-CO~2~: supercritical CO~2~, TPP: three-phase partitioning. Mean values ± SD with different letters are significantly different (Tukey test, α = 0.05, *n* = 3). foods-08-00572-t006_Table 6 ###### Comparison of protein extraction yield and purity between edible insect and several pulse matrices. -------------------------------------------------------------------------------------------------------------------------------------------------------------------- Protein Source Extraction Method Protein Extraction Yield\ Protein Purity\ Reference (%) (%) ------------------------ ----------------------------------------------------------------- --------------------------- ----------------- --------------------------- *A. domesticus* ^1^ Alkaline solubilization and isoelectric precipitation 31.0--38.9 58.3--78.5 *T. molitor* ^1^ Alkaline solubilization and isoelectric precipitation 33.2--39.3 48.7--75.4 Pea Alkali extraction-isoelectric precipitation 62.6--76.7 83.3--86.9 \[[@B29-foods-08-00572]\] Salt extraction 68.2--74.8 71.5--79.3 Micellar precipitation 30.7--31.1 81.9--87.8 Pea Isoelectric precipitation 55.0 81.7 \[[@B30-foods-08-00572]\] Ultrafiltration 57.1 83.9 Lentil Isoelectric precipitation 50.3--62.8 78.2--79.1 Ultrafiltration 51.9--60.5 82.7--88.6 Chickpea Isoelectric precipitation 53.7--69.1 63.9--73.6 Ultrafiltration 50.3--54.7 68.5--76.5 Flaxseed Hydrolysis with cellulase followed by isoelectric precipitation ND 82 \[[@B31-foods-08-00572]\] -------------------------------------------------------------------------------------------------------------------------------------------------------------------- ^1^ Data obtained in the present study. ND: not determined.
3.34375
3
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Q: Simple question regarding factoring quadratics Say we have an equation $ax^2 + bx - c = 0$ and want to find $x$. Obviously the way to solve would be to use the quadratic equation or factorize. I understand that saying $$ax^2 + bx = c => x(ax + b) = c$$ and then solving is wrong (the values of $x$ when subbed back in do not satisfy the eqn), but why is it wrong? Each step seems logical? Many thanks. A: The equation $x(ax+b) = c$ is valid but does not help. There is a general fact that $AB = 0$ implies $A = 0$ or $B=0$ and this allows us to solve a product expression by reducing it to easier equations. So we need 0 on the right hand side of the product to be useful. e.g. we want to rewrite your equation $ax^2 + bx - c = 0$ as $a(x+\alpha)(x+\beta) = 0$. In order to find $\alpha, \beta$ to do this, note that we ensured the quadritic term is already OK: $ax^2$ in both. The linear term is $a(\alpha+\beta) = b$ and the constant term is $a\alpha\beta = -c$. So you need to find $\alpha$ and $\beta$ with known sum $\frac{b}{a}$ and known product $\frac{-c}{a}$, and this can sometimes be seen by inspection for concrete $a,b$ and $c$.
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Using a novel patient-specific stem cell-based therapy, researchers at the National Eye Institute (NEI) prevented blindness in animal models of geographic atrophy, the advanced “dry” form of AMD, which is a leading cause of vision loss among people age 65 and older. The protocols established by the animal study set the stage for a first-in-human clinical trial testing the therapy in people with geographic atrophy, for which there is currently no treatment. “If the clinical trial moves forward, it would be the first ever to test a stem cell-based therapy,” said Kapil Bharti, PhD, Stadtman investigator at the NEI unit on ocular and stem cell translational research. The researchers will take a patient’s own blood cells, and in a lab, convert them into iPS cells capable of becoming any type of cell in the body. The iPS cells are then programmed to become retinal pigment epithelial cells, the type of cell that dies early in the geographic atrophy form of AMD. [National Eye Institute] The authors wrote that, “autologous induced pluripotent stem cell (iPSC)–derived retinal pigment epithelium (RPE) transplantation has been shown to improve visual function in animal models of AMD and is currently being tested in human patients.” The therapy involves taking a patient’s blood cells and, in a lab, converting them into iPS cells, which are programmed to become RPE cells, the type of cell that dies early in the geographic atrophy stage of macular degeneration. RPE cells nurture photoreceptors, the light-sensing cells in the retina. In geographic atrophy, once RPE cells die, photoreceptors eventually also die, resulting in blindness. The therapy is an attempt to shore up the health of remaining photoreceptors by replacing dying RPE with iPSC-derived RPE. Before they are transplanted, the iPSC-derived RPE are grown in tiny sheets one cell thick, replicating their natural structure within the eye. This monolayer of iPSC-derived RPE is grown on a biodegradable scaffold designed to promote the integration of the cells within the retina. A specially designed surgical tool was built for the task of inserting the patch of cells between the RPE and the photoreceptors. A scanning electron micrograph image shows a polarized RPE monolayer on a biodegradable scaffold. The image is colored to highlight the scaffold in blue, three RPE cells (brown), and the apical process of cells in RPE monolayer are light green.[Kapil Bharti, PhD, NEI] One concern about using iPSCs is the possibility of oncogenic mutations that might occur during the cell reprogramming process. In this paper, Ruchi Sharma, PhD, and colleagues at the NEI used CD34+ peripheral blood cells from patients with AMD to generate oncogenic mutation-free clinical-grade iPSCs from three AMD patients. These cells were then used for the production of clinical-grade RPE cell patches. The authors wrote that, “compared to RPE cells in suspension, our biodegradable scaffold approach improved integration and functionality of RPE patches in rats and in a porcine laser-induced RPE injury model that mimics AMD-like eye conditions.” For decades now, stem cells have held the promise of a cure. The transplantation of the RPE patches in rodent and pig models of retinal degeneration showed therapeutic effects. Immunostaining confirmed that the iPSC-derived RPE expressed the gene RPE65, suggesting the lab-made cells had reached a crucial stage of maturity necessary to maintain photoreceptor health. RPE65 is necessary for the regeneration of visual pigment within the photoreceptors and is an essential component for vision. Further tests showed that the transplanted RPE cells were pruning photoreceptors via phagocytosis, another RPE function that helps keep photoreceptors healthy. In addition, electrical responses recorded from photoreceptors rescued by RPE patches were normal; whereas photoreceptors treated with a control empty scaffold had died. For decades now, stem cells have held the promise of a cure. The authors suggested that the production process presented in this paper might accelerate the development of safer iPSC-derived stem cell therapies. The planning of a Phase I clinical trial testing the safety of the iPSC-based therapy for geographic atrophy is underway and will be initiated after U.S. FDA approval.
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Q: Sort an array from right to left without using default functions I was reading about arrays and I'm wondering how can I sort the elements from an array from right to left. For example: n = 10 numbers = [] for i in range(1, n+1): numbers.append(i) print(numbers) How can I show the components from the last one to the very first one (10, 9, 8...) using basics tools like cycles and conditions?. And besides this alternative: for i in range(-1, (-len(numbers) - 1), -1): print(numbers[i]) A: You aren't sorting an array. You are attempting to construct one with a particular ordering. You can do this using range directly. range can be invoked with three arguments start, stop and step. This allows you to construct a range 10, 9, ...: Python 2: numbers = range(10, 0, -1) print numbers Python 3: numbers = list(range(10, 0, -1)) print(numbers) output [10, 9, 8, 7, 6, 5, 4, 3, 2, 1]
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It says here, in Malvino Electronic Principles, that the emitter voltage(AC) is half of the input voltage v1. Why? I understood the the current must be constant at this tail, which contains emitter resistor. Its constant because, there is constant voltage drop across that resistor, and 99% of the Vee is dropped across it, because 2 * 0.7 V of both base-emitter junctions, is negligible. ""It says here, in Malvino Electronic Principles, that the emitter voltage(AC) is half of the input voltage v1. Why? "" no nibbles yet? i've been thinking about it all day... here's my 'poor man's offering'... you already know the necessary facts. So let's work it in your mind. but first simplify it by removing Q2 as a step in our thinking... with no Q2,,, as input to Q1's base rises, more current flows through Q1 so voltage at emitter goes up. In fact -emitter voltage will rise by almost exactly same amount as base did, because Vbe is pretty small. You already knew that. now replace Q2 and observe how differently it works - as input to Q1's base rises, more current flows through Q1 ,so the voltage at emitter still goes up but not quite like before. It's different now because every extra millivolt at emitter is also impressed across Q2's e-b. And in a direction to lower Q2's current which drives emitter voltage back down. Qualitatively that's what is happening. And you knew that too. To see why it's half Vin not 1/100th - let's try this thought... allow for a moment this mild exaggeration: that the "tail" is a constant current source (which it approximates if RsubE is high) now do a Kirchoff's Voltage Law Walk around this loop, for the AC signal. :: start at circuit common and traverse up through V1, in through Q1's b-e and out via Q2's e-b which gets us back to common. -V1 +Vbe(Q1) + Veb(Q2) = 0 V1 = Vbe(Q1) + Veb(Q2) That means for the AC signal the two base-emitter junctions form a voltage divider . Aha - so the signal voltage will divide between them, and emitter node is in middle. you knew that, too... so far as AC signal current goes, the two base emitter junctions are in series. No ac signal current can get out of emitter -emitter node via a constant current source. Not much can get out through that RE if it's respectably high resistance, signal current will take the easier way out through Q2's internal Re. you knew the facts leading to that. So your AC signal voltage is divided between the internal Re's of the two transistors. For a differential amp those transistors would be a matched pair with similar internal resistances. THAT'S why it's half ! learning is mostly discovering what you already knew..... Interesting - with Q2's base commoned, that differential amp amounts to just a common collector stage followed by a common base stage... common collector stage gives it current gain , common base gives voltage gain. [ now at first glance it will look like i missed a sign in that KVL - remember this is small signal analysis not the DC biasing. ] and yes,, op-amps are differential amplifiers. Don't despair you'll be amazed how quickly they make sense. They're not hard to understand, just hard to believe.. . ""It says here, in Malvino Electronic Principles, that the emitter voltage(AC) is half of the input voltage v1. Why? "" no nibbles yet? i've been thinking about it all day... here's my 'poor man's offering'... you already know the necessary facts. So let's work it in your mind. but first simplify it by removing Q2 as a step in our thinking... with no Q2,,, as input to Q1's base rises, more current flows through Q1 so voltage at emitter goes up. In fact -emitter voltage will rise by almost exactly same amount as base did, because Vbe is pretty small. You already knew that. now replace Q2 and observe how differently it works - as input to Q1's base rises, more current flows through Q1 ,so the voltage at emitter still goes up but not quite like before. It's different now because every extra millivolt at emitter is also impressed across Q2's e-b. And in a direction to lower Q2's current which drives emitter voltage back down. Qualitatively that's what is happening. And you knew that too. To see why it's half Vin not 1/100th - let's try this thought... allow for a moment this mild exaggeration: that the "tail" is a constant current source (which it approximates if RsubE is high) now do a Kirchoff's Voltage Law Walk around this loop, for the AC signal. :: start at circuit common and traverse up through V1, in through Q1's b-e and out via Q2's e-b which gets us back to common. -V1 +Vbe(Q1) + Veb(Q2) = 0 V1 = Vbe(Q1) + Veb(Q2) That means for the AC signal the two base-emitter junctions form a voltage divider . Aha - so the signal voltage will divide between them, and emitter node is in middle. you knew that, too... so far as AC signal current goes, the two base emitter junctions are in series. No ac signal current can get out of emitter -emitter node via a constant current source. Not much can get out through that RE if it's respectably high resistance, signal current will take the easier way out through Q2's internal Re. you knew the facts leading to that. So your AC signal voltage is divided between the internal Re's of the two transistors. For a differential amp those transistors would be a matched pair with similar internal resistances. THAT'S why it's half ! learning is mostly discovering what you already knew..... Interesting - with Q2's base commoned, that differential amp amounts to just a common collector stage followed by a common base stage... common collector stage gives it current gain , common base gives voltage gain. [ now at first glance it will look like i missed a sign in that KVL - remember this is small signal analysis not the DC biasing. ] and yes,, op-amps are differential amplifiers. Don't despair you'll be amazed how quickly they make sense. They're not hard to understand, just hard to believe.. . Thank you very much for your in-depth reply. I just finished reading it. I understood every word you said. Thank you very very much. Differential amps are now clear. Now I can move on to op-amps, and nail them. So, does the problem statement say the Rc = Re? Because the gain will only be 1/2 in that case. This is the Vo/Vi gain. Bassalisk's question referred to Ve/Vi gain, which is 1/2 for matched transistors. The common way to do this is with the T small-signal model of a NPN (see link below). Then do a KVL loop from Q1's base to Q2's base (this works because they are both ground referenced). Because there is only the AC source and two matched Re's in the loop the AC voltage at Ve is Vac/2.
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A new study led by researchers at Harvard Medical School identifies key cellular mechanisms that cause blood vessels to age. Now, they're looking for ways to apply what they found in mice studies to human health. Here & Now's Jeremy Hobson talks with David Sinclair (@davidasinclair), the study's senior investigator, a professor and co-director of the Paul F. Glenn Center for the Biology of Aging at Harvard Medical School. Interview Highlights On what the research has found about what happens to blood vessels as they age "Well as I'm sure many listeners know, as we get older we lose our vitality, we become weaker, we're less able to exercise. We just don't feel young anymore, and one of the main reasons for that is that we don't have the blood vessels the blood flowing through our bodies as we used to. And as a result, what happens is that our tissues, our organs, they don't get enough blood supply and they become deficient in oxygen. But also what happens is they can't clear out the toxins. And this combination ends up leaving our tissues and organs susceptible to diseases from liver failure, kidney failure and even dementia. And what we are showing in this new study is that's actually quite reversible, at least in mice, so far." On reversing that aging process "We've been over at Harvard working on this for a number of years, 20 years. We first worked on the red-wine molecule resveratrol. Now we have new molecules that we think are even better. And it turns out it's pretty simple how it works: We've figured out that there are genes in our bodies that respond to exercise and dieting, and we can turn those on with just some small molecules that seem to be safe so far in mice, and even so far safe in humans. "When you give the molecule to the mice, what happens is their bodies — at least the blood vessels — they rejuvenate, they actually become no longer deaf to the signals from muscle. So they behave as though the mice have been exercising, and we have mice that in the lab are 2 years old, which is like 75-, 80-year-old human. And within a few weeks they become as fit and as vital as a young mouse again." On the potential for the study's results to translate to humans "I'm quite optimistic with this one, because our blood vessels work the same way as in mice. This isn't a complicated disease like Alzheimer's. And so I think that actually I'd be surprised if there isn't some benefit in people. Of course the challenge is to make a drug, and we have to make sure it's super safe, but we're already doing human studies over the road from my lab at Harvard. And so far it looks really good." On whether the research would be applied to help treat disease, or get older people to exercise more "This would be both. We're working on having a drug available that your doctor could prescribe for you if you're feeling frail or you have a disease such as muscle wasting, or even diabetes and even dementia, we think that this could be useful. But as a side effect, what we think the patients would notice would be improved stamina when they wake up in the morning, they don't groan anymore. They can get back to exercising, and even people who have been in bed rest or in wheelchairs could potentially even get back to having mobility again." On remaining questions "Mostly I wanna know how safe it is, and those are the studies that are ongoing right now. But hopefully by the end of this year or early next, we'll actually know if the same effects are seen in human subjects, and it's pretty easy to test if somebody gets increased endurance, you don't have to wait years for the outcome. And then hopefully we'll be able to see with further studies if this actually truly reverses aging throughout the body. This molecule that we're giving the patients, or the test subjects, has the potential to actually extend lifespan in the same way it does mice. And so that's really the holy grail here that we're chasing."
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Ability of nucleus cochlear implantees to recognize music. Eight adults with cochlear implants participated in experiments to test their ability to recognize music. Some subjects showed good ability to recognize songs that were sung with instrumental accompaniment but poor ability to recognize songs played on an electronic keyboard without verbal cues, indicating that they were recognizing the songs by verbal cues rather than by musical qualities such as tones and melodic intervals. This conclusion was strengthened by the finding that subjects were barely able to distinguish between songs with the same rhythm and pitch range, and they showed poor ability to discriminate musical intervals. (The closest discrimination was 4 semitones.) Subjects had good ability to distinguish among the synthesized sounds of various musical instruments played on the electronic keyboard. We speculate that subjects could distinguish the various musical instruments in the same way they distinguish among human voices using spectrographic patterns such as formants or maxima.
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A dramatic change is currently on the horizon in the sector of visual display unit and illumination technology. It will be possible to manufacture flat displays or illuminated surfaces with a thickness of less than 0.5 mm. These are notable for many fascinating properties. For example, it will be possible to achieve illuminated surfaces in the form of wallpaper with very low energy consumption. In addition, color visual display units with hitherto unachievable trueness of color, brightness and viewing angle independence will be producible with low weight and very low power consumption. The visual display units will be configurable as microdisplays or large visual display units of several m2 in area, in rigid or flexible form, or else as transmission or reflection displays. In addition, it will be possible to use simple and inexpensive production processes such as screen printing or inkjet printing or vacuum sublimation. This will enable very inexpensive manufacture compared to conventional flat visual display units. This new technology is based on the principle of OLEDs, Organic Light Emitting Diodes, which is shown schematically and in simplified form in FIG. 36. Such components consist predominantly of organic layers, as shown schematically and in simplified form in FIG. 36. At a voltage of, for example, 5 V to 10 V, negative electrons pass from a conductive metal layer, for example from an aluminum cathode, into a thin electron conduction layer and migrate in the direction of the positive anode. This consists, for example, of a transparent but electrically conductive thin indium tin oxide layer, from which positive charge carriers, called holes, migrate into an organic hole conduction layer. These holes move in the opposite direction compared to the electrons, specifically toward the negative cathode. In a middle layer, the emitter layer, which likewise consists of an organic material, there are additionally special emitter molecules where, or close to which, the two charge carriers recombine and lead to uncharged but energetically excited states of the emitter molecules. The excited states then release their energy as bright emission of light, for example in a blue, green or red color. White light emission is also achievable. In some cases, it is also possible to dispense with the emitter layer when the emitter molecules are present in the hole or electron conduction layer. The novel OLED components can be configured with a large area as illumination bodies, or else in exceptionally small form as pixels for displays. A crucial factor for the construction of highly effective OLEDs is the luminous materials used (emitter molecules). These can be implemented in various ways, using purely organic or organometallic molecules, and complexes. It can be shown that the light yield of the OLEDs can be much greater with organometallic substances, called triplet emitters, than for purely organic materials. Due to this property, the further development of the organometallic materials is of high significance. The function of OLEDs has been described very frequently.[i-vi] Using organometallic complexes with high emission quantum yield (transitions including the lowermost triplet states to the singlet ground states), it is possible to achieve a particularly high efficiency of the device. These materials are frequently referred to as triplet emitters or phosphorescent emitters. This has been known for some time.[i-v] For triplet emitters, many property rights have already been applied for and granted.[vii-xix] Copper complexes of the Cu2X2L4, Cu2X2L′2 and Cu2X2L2L′ form (L=phosphane, amine, imine ligand; L′=bidentate phosphane, imine, amine ligand, see below) are already known in the prior art. They exhibit intense luminescence on excitation with UV light. The luminescence can originate either from an MLCT, CC (cluster centered) or XLCT (halogen-to-ligand charge transfer) state, or a combination thereof. Further details of similar Cu(I) systems can be found in the literature.[xx] In the case of the related [Cu2X2(PPh3)2nap] complex (nap=1,8-naphthyridine, X=Br, I), a transition between the molecular orbital of the {Cu2X2} unit (Cu d and halogen p orbitals) and the π* orbitals of the nap group is discussed.[xxi] Triplet emitters have great potential for the generation of light in displays (as pixels) and in illuminated surfaces (for example, as luminous wallpaper). Very many triplet emitter materials have already been patented and are now also being used technologically in first devices. The solutions to date have disadvantages and problems, specifically in the following areas: long-term stability of the emitters in the OLED devices, thermal stability, chemical stability to water and oxygen, availability of important emission colors, manufacturing reproducibility, achievability of high efficiency at high current densities, achievability of very high luminances, high cost of the emitter materials, emitter materials are toxic and syntheses are complex. Accordingly, it was an object of the present invention to overcome at least some of the abovementioned disadvantages.
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A. The POTS Network The Plain Old Telephone Service (POTS) network, which has been in existence for over 100 years, is well designed and well engineered for the transmission and switching of 3 kHz voice calls. The POTS network is a real-time, low-latency, high reliability, moderate fidelity voice telephony network. It is not designed for, nor especially well suited for, other forms of communications, including wideband speech or audio, images, video, fax, and data. The POTS network is inherently “telephone” or “handset” oriented and is driven by the need of real-time voice telephony. There are approximately 270 million users of the POTS network in the United States, making POTS access nearly ubiquitous throughout the US. On the other hand, the POTS network has high access costs, and for international calls, settlement costs. 1. Voice and Signaling Circuits Today's POTS network includes a plurality of subnetworks. The two primary subnetworks are a circuit-switched voice subnetwork and an out-of-band signaling subnetwork. In addition, the POTS network includes other packet subnetworks used for operations and network management functions. The POTS circuit-switched voice subnetwork includes voice-grade circuits that can carry voice signals or data at multiples of a basic 64 kilobits/second rate. The voice subnetwork includes a multiplicity of Service Switching Points (SSP) that are used to set up circuit-switched connections that carry voice traffic or data traffic (i.e., the “payload”) on the POTS network. Each SSP may be a switch used by a Local Exchange Carrier (LEC), such as a 5ESS® switch (5E) made by Lucent, or a switch used by an InterExchange Carrier (IXC), such as a 4ESS® switch (4E) made by Lucent. The POTS signaling subnetwork is itself a packet-switched network, denoted as Signaling System 7 (SS7). The SS7 signaling subnetwork carries digital information which assists in fast call setup and routing, as well as providing transaction capabilities using remote database interaction. The SS7 signaling subnetwork includes a series of paired components connected to an SSP. Typically, each of the paired components for the SS7 signaling subnetwork includes one or more Signal Transfer Points (STP) and one or more Service Control Points (SCP). Each STP and SCP provides, respectively, a router and a database used to implement call setup, call routing, call control and the logic (or programs) and related information functions used to provide advanced communications services over the POTS network. Details of STPs and SCPs, their operation, and how they interact with SSPs are well-understood by those skilled in the art. The SS7 signaling subnetwork also includes a protocol (which, in turn, includes a series of sub-protocols). Thus, for example, under the SS7 protocol, it is possible to automatically transfer information about the calling party to the called party (i.e., the so-called “Caller ID”). Furthermore, e.g., the SS7 signaling subnetwork and protocol interacts with the voice subnetwork so as to enable a query from an SSP in the voice subnetwork to a Service Control Point (SCP) database in the SS7 subnetwork for determining how to route a call, such as a toll-free (e.g., “800“1) call. Thus, e.g., the SCP can return to the SSP a routing number corresponding to the dialed “800” number. Additional call features or services utilizing the interaction capabilities of the voice and signaling subnetwork of the POTS network are well known. 2. Interactive Voice Response Systems Using known interactive voice response (IVR) techniques, callers can directly update database records or select specific information for retrieval by, e.g., entering touch-tones or using voice commands. Retrieved textual information can be converted to speech and played over the phone, or sent directly to the caller as a fax document. As a result, customers can access information or place orders at their convenience without waiting for a service representative. Businesses benefit by reducing costs associated with attendants and service representatives and by increasing customer satisfaction. B. Packet Networks Packet networks are general-purpose data networks which are not tied to fixed-bandwidth circuits. Instead, they are designed to transmit bits (in the form of a packet of fixed or variable length) only when there are bits to transmit. Packet networks evolved independently of telephone networks for the purpose of moving bursty, non-real-time data among computers and are distinguished by the property that packet communications are routed by address information contained in the data stream itself. Packet networks are especially well suited for sending stored data of various types, including messages, fax, speech, audio, video and still images, but are not well suited for sending real-time communication signals such as real-time speech, audio, and video signals. Typically, one accesses a packet network through a client program executing on a personal computer (PC), and so packet networks are inherently “PC” oriented, and client/server driven. Packet networks provide access to distributed databases and have excellent search capabilities. There are approximately 30 million users of packet networks in the US; this number of users is growing rapidly and will continue to do so over the next decade. Today, the Internet (the largest and most renowned of the existing packet networks) connects over 4 million computers in some 140 countries. The Internet is implemented using a large variety of connections between those millions of computers. These interconnected computers can support applications, such as electronic mail and the World Wide Web, which facilitate communications between persons across the U.S. or around the globe. Among the connections between computers typically found on the Internet are routers. Routers serve to send packets along to their destination by examining packet headers to determine the destination address; routers often send packets to another router closer to the destination. Access to the Internet may be obtained through a point of presence (POP), typically through a server connected to one of the networks that make up the Internet. A large company or business may establish a POP as its own direct connection to the Internet; individuals or small businesses may typically access the Internet through a service provider which may provide a POP for, potentially, a multitude of individuals and businesses. The Internet's global and exponential growth is common knowledge today. The recent developments of browsers for World Wide Web interfaces and information navigation software, such as a multitude of Web search engines (such as, e.g., Lycos or Alta Vista), coupled with a continuously growing number of public access providers, are making the Internet a fundamental component of the information age, if not the information super highway itself. Users typically communicate over the Internet using a combination of hardware and software providing interconnectivity that is compatible with the standard, namely Transmission Control Protocol/Internet Protocol (TCP/IP). Several alternate forms of communication have developed which utilize either the POTS network or packet networks (and sometimes both). For example, facsimile (fax) communication is now a commonplace option for transmitting copies of documents over the POTS network. Electronic messaging (e.g., e-mail) is a growing phenomenon for those who use a packet network, particularly the Internet, for communications. In addition, many companies today are using packet networks, locally or internally within the company, which are modeled in functionality based upon the Internet. These packet networks, denoted “intranets,” are typically private networks owned or controlled by the company or corporate user. Packets are moved over intranets using the Internet Protocol (IP), and often the same software used in connection with the Internet (e.g., Web browsers) is also used in connection with intranets. Intranet networks are often established to connect to the Internet through a firewall (i.e., a hardware/software combination designed to restrict unauthorized access to the intranet from the outside world). As the Internet grows, more organizations are publishing information on a “site” on the World Wide Web (Web site). Furthermore, generally available and excellent search capabilities can locate a particular piece of information quickly from this globally-distributed database. A World Wide Web site on the Internet typically resides on a computer known as a server, which is accessed through the Internet by a person (or a client) utilizing a computer, such as a PC. A Web site consists of one or more Web pages comprising scripts written in Hyper Text Markup Language (HTML) and typically resides on a server compatible with HyperText Transport Protocol (HTTP, a protocol for interfacing with the Internet). Pages at a Web site are typically accessible and viewed by the person using the PC through software called a Web browser, which typically resides on the person's PC. A Web browser, such as the one by Netscape, interprets Web page HTML scripts to provide a graphical user interface that allows easy access to various services over the Internet. Equivalently, Web sites internal to and locatable over a corporate intranet may be set up and accessed in a like manner using the same or virtually the same software (e.g., a Web browser). Such Web sites internal to a corporate intranet are typically HTTP compatible and addressable using Uniform Resource Locator (URL) techniques, and contain Web pages comprising HTML scripts. Persons may browse the World Wide Web for virtually any kind of information, including information having content derived from one or more media, such as words, sounds or images. Increasingly, businesses are establishing Web sites as a means of providing information to and attracting potential customers, and Web sites are emerging as a means of transacting business. One may locate a company's Web site by, e.g., using one of a number of existing search engines available over the Internet, or browsing other Web sites containing links to the company's Web site, or entering directly the URL, which represents an address for the Web site. Typically, Web browsing takes place in the context of an interactive communication session, where one may, for example, direct the Web browsing session by choosing to follow hypertext links found in Web sites and/or may respond to information located at various Web sites. C. Integration of the POTS and Packet Networks Recently, several new evolutionary systems have emerged with the goal of integrating the POTS and packet networks, including the introduction of packet telephony and “hop-on hop-off” servers. 1. Packet Telephony An Internet-related development is packet telephony. Packet telephony involves the use of a packet network, such as the Internet, for telecommunicating voice, pictures, moving images and multimedia (e.g., voice and pictures) content. Instead of a pair of telephones connected by switched telephone lines, however, packet telephony typically involves the use of a “packet phone” or “Internet phone” at one or both ends of the telephony link, with the information transferred over a packet network using packet switching and packet routing techniques. Packet telephony systems were created with the goal of providing real-time speech communications over packet networks. The basic idea of packet telephony is (1) to use the sound board of a multimedia PC to digitize speech into bits; and (2) to use the processor in the computer to compress the bitstream, packetize it, and then send the result over a packet network to another multimedia PC with the same or equivalent functionality. Although the basic idea is feasible, the resulting real-time voice communications experience is of low quality, albeit at low cost. Some of the drawbacks are: long transmission delays (due to packet size, packet buffering, packet overheads and routing delays) lost and delayed packets (due to network congestion) poor quality of the coded voice (due to the use of low complexity speech coders) difficulty of finding the Internet Protocol (IP) address of the person at the destination need to call people who did not have access to the packet networkSeveral improvements in these areas have been made since the initial introduction of packet telephony, and others have been suggested (e.g., reservation protocols such as RSVP). 2. HOHO Servers As packet telephony grew in popularity, the need to call people who did not have access to the packet network led to the creation of Hop-on Hop-Off (HOHO) servers. The development of Hop-on Hop-Off servers provided a mechanism for PC-initiated telephone calls on a packet network to connect with the POTS network and terminate at a customer's telephone handset or vice-versa. The HOHO or server brings the packet network and POTS network together at a common gateway interface, which bi-directionally converts IP packets into voice and signaling information, such as the sequence of messages used to set up, bridge, and tear down calls. In this way, voice communication is established across the packet and POTS networks. 3. Call Center-Based Telephony Another recent development in linking together the POTS and packet networks is the call center-based system developed by Genesys Telecommunications Laboratories, among others. In a typical call center-based scenario, a customer finds a product/service, while browsing the Web, for which more information is desired. If the particular product/service provider maintains both a Web server and a call center, the customer, along with the Web connection, can be linked to a call center representative in the following way. The customer is asked to click on a button on the PC screen which requests customer information (e.g. home telephone number, name, etc.). The Web server passes the information to the database server in the call center system, which initiates a POTS call to the customer and connects the call to a call center representative. At the same time, the Web page that the customer is looking at may be passed to the call center representative, along with side information such as the length of time that the customer has been looking at the page, the previous pages which have been looked at, etc. In this manner, the customer maintains a voice connection to the call center representative, as well as synchronization between what the call center representative sees on the PC screen and what the customer sees on the PC screen. While the systems described above provide some limited usefulness for individualized applications, none of these systems provide a comprehensive means for combining the POTS network and a packet network (such as the Internet) in a way that takes full advantage of the signaling and real-time signal processing capabilities present in the POTS network. For example, current packet telephony systems do not take advantage of the SS7 signaling subnetwork and protocols to assist call setup and routing. Further, none of the current systems that enable packet telephony using a POTS telephone connection at one or both ends have the capability to intelligently make switching or routing decisions between the POTS network and packet network based upon considerations such as desired quality, time, cost, bandwidth or other considerations. What is desired is a way to combine the POTS network and a packet network, taking full advantage of the signaling capabilities present in the POTS network as well as the addressing capabilities inherent in a packet network, to seamlessly combine the networks for flexible and optimal communications based upon considerations such as desired quality, time, cost or bandwidth.
3.03125
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Nattokinase is a potent fibrinolytic enzyme extracted and highly purified from a traditional Japanese food called Natto. Natto is a fermented cheese-like food that has been used in Japan for over 1000 years for its popular taste and as a folk remedy for heart and vascular diseases. Natto is produced by a fermentation process by adding Bacillus natto, a benefical bacteria, to boiled soybeans. The resulting nattokinase enzyme, is produced when Bacillus natto acts on the soybeans. While other soy foods contain enzymes, it is only the natto preparation that contains the specific nattokinase enzyme. The Discovery of Nattokinase Doctor Hiroyuki Sumi had long researched thrombolytic enzymes searching for a natural agent that could successfully dissolve thrombus associated with cardiac and cerebral infarction (blood clots associated with heart attacks and stroke). Sumi discovered nattokinase in 1980 while working as a researcher and majoring in physiological chemistry at Chicago University Medical School. After testing over 173 natural foods as potential thrombolytic agents, Sumi found what he was looking for when Natto was dropped onto artificial thrombus (fibrin) in a Petri dish and allowed it to stand at 37 C (approximately body temperature). The thrombus around the natto dissolved gradually and had completely dissolved within 18 hours. Sumi named the newly discovered enzyme "nattokinase", which means "enzyme in natto". Sumi commented that nattokinase showed "a potency matched by no other enzyme." 1,7 Potent Thrombolytic Activity The human body produces several types of enzymes for making thrombus, but only one main enzyme for breaking it down and dissolving it - plasmin. The properties of nattokinase closely resemble plasmin. According to Dr. Martin Milner, from the Center for Natural Medicine in Portland, Oregon, what makes nattokinase a particularly potent treatment, is that it enhances the body's natural ability to fight blood clots in several different ways; Because it so closely resembles plasmin, it dissolves fibrin directly. In addition, it also enhances the body's production of both plasmin and other clot-dissolving agents, including urokinase (endogenous). "In some ways, Milner says, nattokinase is actually superior to conventional clot-dissolving drugs. T-PAs (tissue plasminogen activators) like urokinase (the drug), are only effective when taken intravenously and often fail simply because a stroke or heart attack victim's arteries have hardened beyond the point where they can be treated by any other clot-dissolving agent. Nattokinase, however, can help prevent that hardening with an oral dose of as little as 100 mg a day." 1,7 The Prolonged Action of Nattokinase Nattokinase produces a prolonged action (unlike antithrombin drugs that wear off shortly after IV treatment is discontinued) in two ways: it prevents coagulation of blood and it dissolves existing thrombus. Both the efficacy and the prolonged action of NK can be determined by measuring levels of EFA (euglobulin fibrinolytic activity) and FDP (fibrin degradation products), which both become elevated as fibrin is being dissolved. By measuring EFA & FDP levels, activity of NK has been determined to last from 8 to 12 hours. An additional parameter for confirming the action of NK following oral administration is a rise in blood levels of TPA antigen (tissue plasminogen activator), which indicates a release of TPA from the endothelial cells and/or the liver.6,7 The Mechanism Behind Thrombus Blood clots (or thrombi) form when strands of protein called fibrin accumulate in a blood vessel. In the heart, blood clots cause blockage of blood flow to muscle tissue. If blood flow is blocked, the oxygen supply to that tissue is cut off and it eventually dies. This can result in angina and heart attacks. Clots in chambers of the heart can mobilize to the brain. In the brain, blood clots also block blood and oxygen from reaching necessary areas, which can result in senility and/or stroke.1 Thrombolytic enzymes are normally generated in the endothelial cells of the blood vessels. As the body ages, production of these enzymes begins to decline, making blood more prone to coagulation. This mechanism can lead to cardiac or cerebral infarction, as well as other conditions. Since endothelial cells exist throughout the body, such as in the arteries, veins and lymphatic system, poor production of thrombolytic enzymes can lead to the development of thrombotic conditions virtually anywhere in the body.7 It has recently been revealed that thrombotic clogging of the cerebral blood vessels may be a cause of dementia. It has been estimated that sixty percent of senile dementia patients in Japan is caused by thrombus. Thrombotic diseases typically include cerebral hemorrhage, cerebral infarction, cardiac infarction and angina pectoris, and also include diseases caused by blood vessels with lowered flexibility, including senile dementia and diabetes (caused by pancreatic dysfunction). Hemorrhoids are considered a local thrombotic condition. If chronic diseases of the capillaries are also considered, then the number of thrombus related conditions may be much higher. Cardiac infarction patients may have an inherent imbalance in that their thrombolytic enzymes are weaker than their coagulant enzymes. Nattokinase holds great promise to support patients with such inherent weaknesses in a convenient and consistent manner, without side effects.1,6,7 Nattokinase is capable of directly and potently decomposing fibrin as well as activating pro-urokinase (endogenous). Research In The United States Dr. Martin Milner of the Center for Natural Medicine in Portland, Oregon and Dr. Kouhei Makise of the Imadeqawa Makise Clinica in Kyoto, Japan were able to launch a joint research project on nattokinase and write an extensive paper on their findings. "In all my years of research as a professor of cardiovascular and pulmonary medicine, natto and nattokinase represents the most exciting new development in the prevention and treatment of cardiovascular related diseases, "Dr. Milner said." We have finally found a potent natural agent that can thin and dissolve clots effectively, with relative safety and without side effects."1 Animal & Human Studies Nattokinase has been the subject of 17 studies, including two small human trials. Dr. Sumi and his colleagues induced blood clots in male dogs, then orally administered either four capsules of nattokinase (250 mg per capsule) or four placebo capsules to each dog. Angiograms (X-rays of blood vessels) revealed that the dogs who received nattokinase regained normal blood circulation (free of the clot) within five hours of treatment. Blood clots in the dogs who received only placebo showed no sign of dissolving in the 18 hours following treatment.1,3 Researchers from Biotechnology Research Laboratories and JCR Pharmaceuticals Co. of Kobe, Japan, tested nattokinase's ability to dissolve a thrombus in the carotid arteries of rats. Animals treated with nattokinase regained 62 percent of blood flow, whereas those treated with plasmin regained just 15.8 percent of blood flow.1 Researchers from JCR Pharmaceuticals, Oklahoma State University, and Miyazaki Medical College tested nattokinase on 12 healthy Japanese volunteers (6 men and 6 women, between the ages of 21 and 55). They gave the volunteers 200 grams of natto (the food) before breakfast, then tracked fibrinolytic activity through a series of blood plasma tests. The tests indicated that the natto generated a heightened ability to dissolve blood clots: On average, the volunteers' ELT (a measure of how long it takes to dissolve a blood clot) dropped by 48 percent within two hours of treatment, and volunteers retained an enhanced ability to dissolve blood clots for 2 to 8 hours. As a control, researchers later fed the same amount of boiled soybeans to the same volunteers and tracked their fibrinolytic activity. The tests showed no significant change.1,3,6 The Benefits of Nattokinase on Blood Pressure Traditionaly in Japan, Natto has been consumed not only for cardiovascular support, but also to lower blood pressure. In recent years, this traditional belief has been confirmed by several clinical trials. In 1995, researchers from Miyazaki Medical College and Kurashiki University of Science and Arts in Japan studied the effects of nattokinase on blood pressure in both animal and human subjects (see below). In addition, the researchers confirmed the presence of inhibitors of angiotensin converting enzyme (ACE), which converts angiotensin I to its active form angiotensin II within the test extract, which consisted of 80% ethanol extract of lyophilized viscous materials of natto. ACE causes blood vessels to narrow and blood pressure to rise - by inhibiting ACE, nattokinase has a lowering effect on blood pressure.1,2 Animal Study After a single intraperitoneal administration of 400-450 grams of the test extract (equivalent to 25 mg of natto food) into male Wister rats, systolic blood pressure (SBP) significantly decreased from 166 + mmHg to 145 + 24 mmHg in just two hours (p<0.05), and decreased further to 144 + 27 mmHg in 3 hours (p<0.05). On average, this data represents a 12.7 percent drop in SBP within two hours.1,2 Human Study The same natto extract was then tested on human volunteers with high blood pressure. Blood pressure levels were measured after 30 grams of lyophilized extract (equivalent to 200 grams of natto food) was administered orally for 4 consecutive days. In 4 out of 5 volunteers, the systolic blood pressure (SBP) decreased on average from 173.8 + 20.5 mmHg to 154.8 + 12.6 mmHg. Diastolic blood pressure (DBP) decreased on average from 101.0 + 11.4 mmHg to 91.2 + 6.6 mmHg. On average, this data represents a 10.9 percent drop in SBP and a 9.7 percent drop in DBP.1,2,6 Conclusion The traditional Japanese food Natto has been used safely for over 1000 years. The potent fibrinolytic enzyme nattokinase appears to be safe based upon the long-term traditional use of this food. Nattokinase has many benefits including convenience of oral administration, confirmed efficacy, prolonged effects, cost effectiveness, and can be used preventatively. It is a naturally occurring, food based dietary supplement that has demonstrated stability in the gastrointestinal tract, as well as to changes in pH and temperature. Glossary of Terms: Cardiac Infarction: Heart attack. Cerebral Infarction: Stroke. Fibrin: A whitish, filamentous protein formed by the action of thrombin on fibrinogen and makes up part of coagulum or blood clots. Fibrinolytic: Pertaining to or causing the breaking up of blood clots. Infarction: Cardiac or cerebral tissue death due to failure of blood supply to the area usually caused by a blood clot. Plasmin: An endogenously produced fibrinolytic enzyme. Plasminogen: A precursor to plasmin. A protein found in many tissues and body fluids. Thrombus: A blood clot that obstructs a blood vessel or a cavity of the heart. Thrombolytic: Pertaining to or causing the breaking up of a thrombus. TPA: Tissue plasminogen activator. t-PAs: The most commonly used thrombolytic drugs including activase, urokinase, and streptokinase. Urokinase: An endogenously produced thrombolytic enzyme & also a commonly used thrombolytic drug given intravenously to cardiac and cerbral infarction patients. A mutant of Bacillus subtilis IMR-NK1, which is used for the production of domestic "natto" in Taiwan, produced high fibrinolytic enzyme activity by solid-state fermentation using wheat bran as medium. Purification and characterization of a fibrinolytic enzyme produced from Bacillus sp. strain CK 11-4 screened from Chungkook-Jang. Nattokinase is a new fibrinolytic enzyme which cleaves directly cross-linked fibrin in vitro. In this study, we investigated the thrombolytic effect of nattokinase on a thrombus in the common carotid artery of rat in which the endothelial cells of the vessel wall were injured by acetic acid. When a section of occluded vessel was stained for CD61 antigen by immunofluorescence utilizing a monoclonal antibody, the antigen was localized around the surface of the occluded blood vessels. This result suggests that the occlusive thrombosis was caused by platelet aggregation. In addition, thrombolysis with urokinase (UK; 50000 IU/kg, i.v.) or tissue plasminogen activator (tPA; 13300 IU/kg, i.v.) in our model was observed to restore the blood flow over a 60 min monitoring period. The results indicate that our chemically induced model is useful for screening and evaluating a thrombolytic agent. We evaluated the thrombolytic activity of nattokinase using this model and compared it with fibrino(geno)lytic enzyme, plasmin or elastase. On a molar basis, the recovery of the arterial blood flow with nattokinase, plasmin and elastase were 62.0 +/- 5.3%, 15.8 +/- 0.7% and 0%, respectively. The results indicate that the thrombolytic activity of nattokinase is stronger than that of plasmin or elastase in vivo. Intraduodenal administration of nattokinase (NK) at a dose of 80 mg/kg, resulted in the degradation of fibrinogen in plasma suggesting transport of NK across the intestinal tract in normal rats. The action of NK on the cleavage of fibrinogen in the plasma from blood samples drawn at intervals after intraduodenal administration of the enzyme was investigated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting analysis with an anti-fibrinogen gamma chain antibody. In parallel with the degradation process, plasma recalcification times were remarkably prolonged NK was also detected in the plasma from blood samples drawn 3 and 5 h after administration of the enzyme by SDS-PAGE and Western blotting analysis with an anti-NK antibody. The results indicate that NK is absorbed from the rat intestinal tract and that NK cleaves fibrinogen in plasma after intraduodenal administration of the enzyme. Purification and characterization of a strong fibrinolytic enzyme (nattokinase) in the vegetable cheese natto, a popular soybean fermented food in Japan. A strong fibrinolytic enzyme (nattokinase) was purified from the vegetable cheese natto. Nattokinase was extracted from natto with saline and isolated by sequential use of hydrophobic chromatography. The isolated protein gave a single sharp band on SDS-PAGE either before or after reduction. The sequence, as determined by automated Edman degradation of the uncleaved molecule and its enzymatically derived peptide, consisted of a total 275 amino acid residues (M.W = 27,728) and exhibited a high homology with the subtilisins. Enhancement of the fibrinolytic activity in plasma by oral administration of nattokinase. The existence of a potent fibrinolytic enzyme (nattokinase, NK) in the traditional fermented food called 'natto', was reported by us previously. It was confirmed that oral administration of NK (or natto) produced a mild and frequent enhancement of the fibrinolytic activity in the plasma, as indicated by the fibrinolytic parameters, and the production of tissue plasminogen activator. NK capsules were also administered orally to dogs with experimentally induced thrombosis, and lysis of the thrombi was observed by angiography. The results obtained suggest that NK represents a possible compound for use not only in the treatment of embolism but also in the prevention of the disease, since NK has a proven safety and can be massproduced. A novel fibrinolytic enzyme (nattokinase) in the vegetable cheese Natto; a typical and popular soybean food in the Japanese diet. A strong fibrinolytic activity was demonstrated in the vegetable cheese Natto, which is a typical soybean food eaten in Japan. The average activity was calculated at about 40 CU (plasmin units)/g wet weight. This novel fibrinolytic enzyme, named nattokinase, was easily extracted with saline. Nattokinase not only digested fibrin but also the plasmin substrate H-D-Val-Leu-Lys-pNA (S-2251). These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. It is imperative that Nattokinase is processed and stored by specific guideline to maintain maximum results in the body. For further help go to Serraflazyme, an extraordinary enzyme - Ecological Formulas (Cardiovascular Research) - http://www.healingedge.net/store/ecological-ss8.html#363 Isolated, purified and encapsulated nattokinase, an enzyme derived from boiled soybeans and Bacillus subtilis natto. Nattokinase NSK-SD® was the first nattokinase introduced into the US market, and it has established standardization and quality levels for all nattokinase, with comprehensive safety studies and proven potency. It is vegetarian, non-irradiated, and free of vitamin K2. NSK-SD® has two Japanese and three U.S. patents, and is recognized by the JHFA (Japan Health and Nutrition Food Authorization) and JNKA (Japan Nattokinase Association) as authentic nattokinase. Each batch is tested to ensure potency. NSK-SD® is a trademark of Japan BioScience Laboratory. Shop the Products Company Help Please note that the material within Healing*Edge Science is for educational purposes only and should not be replaced by a physician's consultation. The Food and Drug administration has not evaluated this information or any other information on integrative medicine. Copyright and trademark laws under U.S. and international law protect this site. All information, images, layout and design in part or whole, cannot be copied or used for business purposes, without first requesting permission from Healing*Edge Sciences.
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The invention concerns tools for turning, and especially tools for fashioning deep and/or hollow work in materials such as wood, plastics, soft metals and alabaster. In recent years there has been a resurgence of interest in the art and craft of wood turning, including a particular interest in producing larger vessels of both the "deep" and "hollow" types. Usually the term deep refers to a cavity the internal diameter of which decreases progressively from the mouth to the bottom of the cavity. A simple example is an open cone. The term hollow refers to vessels in which there is at least one internal chamber with a mouth or entrance of smaller diameter than the maximum internal diameter of the chamber. A simple example is a sphere with a circular opening. Two of the problems facing the turner desiring to fashion deep or hollow vessels significantly larger than those feasible and economical with conventional tools, are the volumes of material to be removed and the much greater reach of tool required. Typically these attempts at larger vessels have been made using somewhat makeshift adaptations of conventional methods and tools. The conventional way of removing redundant material is by comminution (reducing all of the material to shavings or sawdust) for example with a gouge tool. The rough forming of an extra large vessel in this way can be very laborious, time consuming and wasteful of the raw material. (Doubling the principal dimensions of a vessel increases its volume and hence the volume of material to be worked eight times.) The second problem is the control of tools at the greater reaches involved in fashioning the inside of larger vessels. With the cutting edges of the tool more remote from the tool rest it becomes more difficult to control the tool for accurate work. A simple lengthening of the tool handle may help in holding the tool against the greater leverage resulting from increased tool reach. But typically no provision is made for holding the tool against the increased torsion forces experienced at the tool handle, especially when an offset tool is used. A conventional tool such as a round nosed scraper may be used in a "slicing" operation to remove some volume of material, as for example in removing a cone from the end of a workpiece at the beginning of fashioning the internal form of a vessel. But the width of such tools (typically about one inch wide) wastes much material in the cuts and the operation is time consuming and inefficient. With conventional tools, usable reach beyond the tool rest is typically of the order of two to three inches. With some adaptation greater reaches are possible, but usually only in a fatiguing operation without satisfactory control or efficiency.
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Justification:Acacia bifaria is a small shrub with a restricted distribution in mallee of Western Australia between Ravensthorpe and Fitzgerald River. This shrub is only known from approximately six localities and mostly distributed outside protected areas in a highly fragmented habitat due to clearing for agriculture. The extent of occurrence warrants this species a listing of Endangered (EOO ~3,700 km²). Changes in fire regimes, increased salinity, mining activities and grazing pressure are threatening processes to this habitat. Furthermore, despite some populations known from the Fitzgerald National Park, there are concerns over the devastating effects that the pathogen Phytophthora cinnamomi might have on the vegetation of the area if the spread of this disease is not contained. If the current management measures to contain the spread are not successful there is a high risk that some subpopulations will become extinct. It is recommended that monitoring of the habitat status, threats and pathogen are continued. Acacia bifaria is endemic to Australia, only known from Ravensthorpe to the Fitzgerald River (c. 30 km east of Jerramungup) in southwestern Western Australia. Recent surveys conducted around Wellstead found the species in in the area (Ecologia Environment 2008). There are no direct threats to the species, however, according to the Biodiversity Assessment carried out for the Australian Natural Resources Atlas, the condition of the Esperance Plains region, where this species occurs, is fair to poor with a declining trend generally. Threatening processes to the area include vegetation clearing and fragmentation for agriculture, hydrological changes and salinity, feral predators and herbivores, grazing by stock and weeds. Many communities and species are localized in occurrence and vulnerable to fire events. In the Esperance region (ESP1 Fitzgerald subregion) approximately half of it has been cleared of native vegetation and agriculturally productive landscapes are now almost completely cleared (Comer et al. 2001). Despite the fact that this species is not susceptible to root-rot fungus (Groves et al. 2009) Phytophthera is changing the composition of coastal heath and scrub communities (Australian Natural Resources Atlas 2009). Most importantly, recent news reports warn that dieback root-disease is posed to tear through the Fitzgerald National Park, despite efforts from the Project Dieback to contain the spread of the pathogen (Bennet 2010). Dr. Chris Dunne from the Dieback Working Group (2009) reported that ‘The research indicates that the impacts of the disease along the south-coast are likely to be even more significant than in the Jarrah forest where the disease was first observed to cause mass collapse of forest sites. Extreme weather events, such as summer rainfall linked to northern cyclone activities, can lead to a significant spread of dieback and a mass collapse in these native vegetation sites”. Some populations are also threatened by mining activities, the species is found in proposed site for an open pit Magnetite mine (Ecologia Environment 2008) and in exiting mines in Elverdton-Desmond area (Department of Industry and Resurces; Department of Mines and Petroleum). Although most collections do not appear to be within protected areas, this species is known to occur within the Fitzgerald River National Park. It is listed as 2KC- in Briggs and Leigh (1995) a poorly known taxon with a geographic range less than 100 km2 that is known to occur within a reserved but the population size is not known. It is also listed as Priority 3 in Smith (2010) taxa which are known from several populations, at least some of which are not believed to be under immediate threat.
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A sixth-century Irish headache cure and its use in a south German monastery. Medieval headache treatment is largely unknown. Medieval incantations against headache enumerate bodily organs to be protected. One 8th-century Latin hymn from Lake Constance using this device is addressed to St. Aid "mechprech", who has been identified as Aed Mac Bricc, Bishop of Killare, 6th century. This Irish Saint inspired unusual legends by some rather unorthodox activities: He abducted a young girl as hostage while his inheritance was withheld, but at the same time was seen surrounded by angels. He prayed for a nun who was pregnant and made the pregnancy vanish by a miracle, and he replaced the severed heads of maids, men and horses, creating a new spring as a by-product of this operation. Already at his birth his head had hit a stone, leaving a hole in the stone which collected rainwater that cured all ailments. In our own time, such "bullaun stones" are still believed to cure headache in Ireland. According to the legends collected by Plummer and Colgan, St. Aed Mac Bricc was well known for his power to cure headaches. He relieved St. Brigid's headache when she was suffering many miles away, but his most impressive cure was in convincing a headache sufferer that the patient's headache could actually be transferred own head. The headache hymn or incantation is intended to repeat Aed's unique miracle.
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Pre_GI: SWBIT SVG BLASTP Query: NC_011274:4385039 Salmonella enterica subsp. enterica serovar Gallinarum str. 287/91Lineage: Salmonella enterica; Salmonella; Enterobacteriaceae; Enterobacteriales; Proteobacteria; BacteriaGeneral Information: Salmonella gallinarum is the causative agent of Fowl typhoid, a severe systemic disease of poultry. This group of Enterobactericiae have pathogenic characteristics and are one of the most common causes of enteric infections (food poisoning) worldwide. They were named after the scientist Dr. Daniel Salmon who isolated the first organism, Salmonella choleraesuis, from the intestine of a pig. The presence of several pathogenicity islands (PAIs) that encode various virulence factors allows Salmonella spp. to colonize and infect host organisms. There are two important PAIs, Salmonella pathogenicity island 1 and 2 (SPI-1 and SPI-2) that encode two different type III secretion systems for the delivery of effector molecules into the host cell that result in internalization of the bacteria which then leads to systemic spread. General Information: This organsim is a sulfur-oxidizing bacterium isolated isolated from estuarine mud in the Netherlands. Sulfur-oxidizing bacterium. Sulfurimonas denitrificans, formerly Thiomicrospira denitrificans, is a denitrifying chemolithoautotroph that uses sulfide or thiosulfate and nitrate or nitrite as the electron donor and acceptor. This organism has been identified in hydrothermal vent areas and from oilfields and may play a role in the cycling of sulfur in these environments.
3.15625
3
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Offer curve In economics and particularly in international trade, an offer curve shows the quantity of one type of product that an agent will export ("offer") for each quantity of another type of product that it imports. The offer curve was first derived by English economists Edgeworth and Marshall to help explain international trade. The offer curve is derived from the country's PPF. We describe a Country named K which enjoys both goods Y and X. It is slightly better at producing good X, but wants to consume both goods. It wants to consume at point C or higher (above the PPF). Country K starts in Autarky at point C. At point C, country K can produce (and consume) 3 Y for 5 X. As trade begins with another country, and country K begins to specialize in producing good X. When it produces at point B, it can trade with the other country and consume at point S. We now look at our Offer curve and draw a ray at the level 5 Y for 7 X. When full specialization occurs, K then produces at point A, trades and then consumes at point T. The price has reduced to 1 Y for 1 X, and the economy is now at equilibrium. References Salvatore, Dominick. "International Economics." John Wiley & Sons, Inc, 2001. Category:International economics Category:Microeconomics Category:Economics curves
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Tag: per-capita output From 1900 to 1980, 70–80 percent of the global production of goods and services was concentrated in Europe and America, which incontestably dominated the rest of the world. By 2010, the European–American share had declined to roughly 50 percent, or approximately the same level as in 1860. In all probability, it will continue to fall and may go as low as 20–30 percent at some point in the twenty-first century. This was the level maintained up to the turn of the nineteenth century and would be consistent with the European–American share of the world’s population. In other words, the lead that Europe and America achieved during the Industrial Revolution allowed these two regions to claim a share of global output that was two to three times greater than their share of the world’s population simply because their output per capita was two to three times greater than the global average. All signs are that this phase of divergence in per capita output is over and that we have embarked on a period of convergence.
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The Neuroscience Revolution Will Be Crowdsourced The editors of Scientific American MIND regularly encounter perspectives on science and technology that we believe our readers would find thought-provoking, fascinating, debatable and challenging. The MIND Guest blog is a forum for such opinions. The views expressed belong to the author and are not necessarily shared by Scientific American. Follow on Twitter @sciammind. Ben Thomas is an author, journalist, inventor and independent researcher who studies consciousness and the brain. A lifelong lover of all things mysterious and unexplained, he weaves tales from the frontiers of science into videos, podcasts and unique multimedia events. Lots more of his work is available at http://the-connectome.com. Follow on Twitter @theconnectome. As Albert Einstein famously said, “No problem can be solved from the same level of consciousness that created it.” The history of science is littered with so-called “intractable” problems that researchers later cracked wide open using techniques their ancestors could hardly imagine. Biologists in the 1950s looked at the staggeringly complex (and beautiful) three-dimensional shapes into which proteins fold and declared that a reliably predictive mathematical model of these convolutions might be unachievable in our lifetimes. But over the past few years, folks with home computers have joined forces to crack many longstanding protein-folding problems using the online game FoldIt. Instead of relying on the number-crunching power of a single supercomputer or network, crowdsourced games like FoldIt translate vast and complex data sets into simple online interfaces that anyone can learn to operate. The crowdsourced astronomy game Galaxy Zoo also depends on an army of “citizen scientists” for classification of stars hundreds of light years away; while Google built its image search technology on an image-labeling game. In fact, every time you “verify your humanity” on a web form by typing out nonsensical reCAPTCHA text, you’re actually helping Google transcribe books from the world’s libraries into a digital format. And now, a worldwide team of neuroscience researchers have begun using this crowdsource approach to crack open one of the greatest problems in any scientific field: The construction of a complete wiring diagram for a mammalian brain. Complexity and simplification Neuroscientists often compare the task of mapping the brain’s wiring to that of untangling all the cords piled up beneath your desk. It’s just that a human brain contains upward of 84 billion “cords” – nerve cells known as neurons – every one of them sporting multiple “plugs” – connections known as synapses – adding up to as many as 100 trillion (that’s “trillion” with a “t”) interconnections in a single brain. MIT's Sebastian Seung (far left) and his research group teamed up with (from left to right) Viren Jain, Winfried Denk, Moritz Helmstaedter, Kevin Briggman and Srini Turaga to map the brain's microstructure with an innovative toolbox of techniques. Throw in the fact that many of these connections are shifting and changing every day, and you can begin to see why some scientists claim that a complete model of a human connectome – a functional map of every neural connection in a human nervous system – is little more than a sci-fi dream right now. Still, a brain is a finite physical object. Its complexity is enormous, but not ineffable. It can be subdivided into lobes, areas and layers. And just as each level of the ocean and forest is home to its own unique range of life, each layer of the cortex is home mainly to a limited range of specific neuron types, each of which cooperates and competes with others in specific ways. “If I just told you, ‘There are a lot of trees in a jungle,’ that’d be true, but it’d be a very crude description, because trees come in many different species,” says Sebastian Seung, a neuroscientist at Massachusetts Institute of Technology. “In the same way, neurons come in many cell types, and one of the important tasks in neuroscience today is to identify and enumerate all these different types of neurons in the brain. Nobody knows how many there are.” This neuron jungle might sound like yet another daunting problem – but in fact, Seung thinks it may provide a simple yet highly accurate way of modeling brain function down at the cellular level. It’s a bit like saying, “We’ll never be able to model the workings of every individual tree in the whole forest – but we don’t have to. All we’ve got to do is understand the behavior of each species.” Even this is no small task; but Seung and his team have found an innovative way to tackle it. Solving the unsolvable Mapping a human connectome demands some conceptual steps up from traditional brain-scanning techniques like fMRI and EEG. So this year, Seung and his colleagues at MIT, along with Moritz Helmstaedter and Winfried Denk at Germany’s Max-Planck Institute for Medical Research, set to work on the problem from a new angle. The international team succeeded in mapping the precise shapes and points of contact between every single one of the 950 neurons in a block of mouse retina - a first-time achievement in the history of neuroscience. The researchers chose a very small chunk of nerve tissue – a tiny slice of retina, to be exact – and looked for an efficient way to tease apart its wiring while preserving its structure. “If we take human colorings or tracings of neurons, and we train the computer to emulate them, the computer still makes mistakes,” Seung explains. “So somehow we have to correct the mistakes of the computer – we have to combine human intelligence and artificial intelligence in order to solve this problem.” The new approach works like this: First, a human operator works through digital slice after slice of brain matter, using computerized tools to draw a “skeleton” of each neuron he or she notices in each slice – similarly to the way computer animators start by drawing a stick figure of an animated character. Once humans have drawn in these neuronal skeletons, an automated computer algorithm builds out a 3D model of each neuron’s three-dimensional shape. “If people had to color in the full three-dimensional shape of a neuron, instead of just drawing the skeleton, each neuron would take ten to 100 times longer, and the cost of our study could’ve been has high as $10 million,” Seung says. But using this new technique, the international team was able to complete the project at a much lower budget, in a matter of mere months. In a recent paper published in the journal Nature, Seung and his colleagues at the Max-Planck Institute unveiled their first major success using this approach: A connectomic map of every neuron in a tiny patch of mouse retina. Along the way, the team discovered several new types of neurons, and generated a neuronal wiring map of unprecedented scale and complexity. Exciting as this retina-mapping project has been, Seung says, it’s only the beginning of his team’s quest for the ultimate goal: A complete map of a human connectome. And to get there, they’re going to need your help. Crowdsourcing a revolution Last year, Seung’s lab rolled out a game called EyeWire. The principle is simple: After a few practice rounds, anyone with a computer and an Internet connection can help researchers map the shapes of actual neurons. In the game, these neurons come with their “skeletons” pre-drawn, and players take on the task of coloring in the neurons’ 3D shapes. Seung and his research assistants developed the crowdsource game EyeWire to enable anyone with a home computer and an Internet connection to help map the trillions of neural connections in a mammalian brain. Computers and neuroscience experts then compare the results; and if all goes well, the result is a map of a synapse that’s never been mapped before – a brand-new brain discovery made by people just like you.“That makes it a multiplayer game,” Seung says. “People are rewarded for giving the same answers as others, and that’s how they learn. That’s how they’re incentivized to be accurate – and it also makes the game inherently social.” Seung’s lab is currently putting together the first journal paper documenting brand-new discoveries made with EyeWire. The researchers aim to use this wealth of data to crack another puzzle: How groups of neurons detect motion. “People want us neuroscientists to explain consciousness,” Seung says; “they want us to cure autism. But in fact, for more than 60 years, neuroscientists have been unable to explain how it is that neurons in the retina can detect motion.” It’s a sobering fact, but one with a silver lining: Thanks to citizen-scientists working through EyeWire puzzles, Seung thinks he and his team have hit on at least one testable explanation of this longstanding neuroscience mystery. To find out what they’ve discovered, though, we’ll have to wait for the upcoming paper. EyeWire players have already mapped a large number of neurons – and mapping new ones every day – but it’s still clear that long years of work lie between us and our goal of a complete human connectome. The data gathered so far may seem like drop of water in the ocean, but projects like EyeWire are actually proofs-of-concept for a technique of extraordinary power. “It’s clear that is now possible – not easy, but entirely possible – to start mapping mammalian connectomes at the cellular level,” Seung says. “The technology wasn’t there just a few years ago, but technology is advancing rapidly.” Images: Sebastian Seung About the Author: Ben Thomas is an author, journalist, inventor and independent researcher who studies consciousness and the brain. A lifelong lover of all things mysterious and unexplained, he weaves tales from the frontiers of science into videos, podcasts and unique multimedia events. Lots more of his work is available at http://the-connectome.com. Follow on Twitter @theconnectome. 5 Comments Okay, good stuff — but I don’t believe that the Neuroscience Revolution is going to come from increasing information about brain structure, however detailed it might be. What is delaying the revolution is the weakness of our ability to observe the dynamic activity of populations of brain cells. Along similar lines as the first commentator, having a schematic diagram of the processor circuitry in the device I’m using to access this article allows an enormous variety of software programs to be executing – having the circuit diagram or even an electrical signal trace provides at best little meaningful information regarding the software that is currently executing. IMO, the human brain is far more than the neural circuit interconnections and chemical microenvironments that control the flow of its electrical signals. The signals it produces also produce the modification of those chemical environments and electrical circuits – it is self-adapting… What “Neuroscience Revolution” is envisioned, given the exceedingly limited scope of current neuroscience? I often think celebrity quotes are incorrect, such as Einstein’s in this case. Although I like Albert, his quote doesn’t stand up, say, to the case of Thomas Edison when he made the first electric light. Indeed, he used the same process relentlessly…but tried the process on over 10,000 substances…finally arriving at Tungsten, which was a winner. So, in Edison’s case, persistence at effort…from a certain,unchanging, conscious view…was in fact the right thing to do. Sorry Albert. Nearly all Celebrity quotes can be tossed the other way…Right? Also, Counting and Mapping Neurons has actually become a scientific prejudice…believe it or not. When Obama gave a large sum of money to the Brain Initiative as it was called…it was quickly pointed out…that the Initiative was going to totally blow by…or omit…the tremendous importantance of Glial cell/calcium Ion messaging. Synapse is not a neuron cell monopoly, right? I think what Seung is saying…is echoed in many other neurological circles…there really is no effective brain or consciousness theory at the moment. This will probably play out like the physics search for a TOE…a theory of everything for all Fields. In fact, TOE’s themselves will begin to multiple in multiple fields…as more funding and energy are provided. Eventually, all carpenters will have their own hammers…and see the Big U in that light. It’s a bit relative, right?
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You can still make your voice heard by talking about domestic and family violence with those around you in person and on social, or if you’re not sure what to say, share one of the entries to our competition. Why we’ve used a music competition to #stopthehurting and #enddomesticviolence Why do kids and teenagers need to know about domestic and family violence? Understanding what domestic violence looks like and why it’s unhealthy can help stop the cycle of abuse – help prevent young people enacting this behaviour as adults. Even if they don’t want to replicate the behaviour, subconsciously it can become a norm based on the role modelling they grew up with. It’s also important to bring the issue out from behind closed doors and recognize there’s nothing shameful about being in this situation, and it’s one that unfortunately a lot of kids find themselves in. Even if someone hasn’t experienced domestic and family violence, having a clearer understanding will help them support and understand others. This campaign was created by kids for kids in collaborative workshops. They shared their perceptions, insights, preferred communication approaches, what they knew and what they wanted to know about domestic and family violence. They made their voices heard.
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Human or animal tissue is susceptible to many forms of damage. The damage can have many causes, including: non-complicated acute wounding, complicated chronic wounding, trauma, exercise related trauma and pathological damage. An example of non-complicated acute wounding is a wound caused by surgery. Complicated chronic wounding may include wounds such as diabetic and venous ulcers, pressure sores and burns. Trauma wounds may include lacerations, contusions, incisions and blunt trauma such as bullet injuries. Exercise related trauma may occur to muscles, tendons and ligaments as a result of overuse, misuse and abuse. Pathological damage may cause joint problems, such as osteo-artritis and rheumatoid arthritis. Repair of damaged tissue involves regeneration of tissue cells which occurs naturally as a result of repair mechanisms in the human or animal body. Often the natural repair of damaged tissue can be a lengthy process or does not occur at all as a result of the debilitating effects of infection or permanent damage to the tissue repair mechanisms. The time taken to repair damaged tissue can cause many related problems, such as infection or re-infection of the damaged tissue, prolonged pain, temporary or permanent disability, scarring or aesthetic embarrassment for the injured person. For athletes and animals, such as horses, tissue damage prevents participation in training or competitions. Thus, it is advantageous to provide a device for treating damaged tissue that promotes faster tissue repair. Dressings for promoting tissue repair have been known for many years. These dressings are coated with substances which are absorbed into the damaged tissue and actively encourage cellular regeneration and prevent infection. However, such dressings only provide a slight improvement in the speed of the healing process. In the case of serious trauma or large areas of wounding, such dressings can become ineffectual and, in some cases, create more damage, for example by preventing oxygen getting to the surface of the wound. In the case of muscle, ligament or tendon damage, such dressings have no therapeutic effect at all, except to act as a support to the damaged area whilst repair occurs naturally. In recent years, electrical treatment of damaged tissue has become known as an effective method of treatment of damaged tissue. This method involves supplying electrical current to a treatment area (i.e. either directly to the external wound or to the surface of the skin near the damaged tissue). Electrodes are fixed to the treatment area and a current generating device is connected to the electrodes. Originally, these devices supplied current at a fixed amplitude ranging from 1 to 10 milliamps. It was found that supplying current via electrodes to the treatment area significantly improved the time taken to repair damaged tissue. However, supplying current at such levels can result in discomfort for the user of the device. Therefore, more recent developments have included supplying electrical current to the surface of a treatment area with a constant amplitude waveform typically having an amplitude in the range of 10 to 800 microamps. Electrical current in this range is commonly known as “micro-current” and the electrical stimulation it causes cannot generally be detected by a user of the device. Some existing current generating devices for supplying current to electrodes fixed to a treatment area are described in PCT Publication Nos. 00/02622, 01/03768, 98/23326 and 98/40121 and U.S. Pat. No. 5,395,398. All of the current generating devices described in the aforementioned documents comprise a remote unit with attached electrodes. The electrodes must be fixed to the treatment area, typically with tape. Wires connect the electrodes to the current generating unit which is remote from the treatment area. Treatment with such devices requires specialist knowledge about the operation of the device and electrodes, including knowing where to locate the electrodes and how to connect them to the current generating device. This often necessitates frequent visits to clinics by a user of the device. Furthermore, there is the annoyance of having to carry a separate current generating unit. Generally, the user has to remain immobile whilst treatment is being carried out. PCT Publication No. 94/22529 describes an elastic housing with electrodes sewn into specific positions which can be worn by a user. When the housing is worn by a user, the electrodes are in the correct anatomic position for optimal treatment of the tissue which is to be treated. A current generating unit is fixed to the housing by insertion into a small pocket on the housing. The current generating unit is connected to the electrodes and supplies current to the electrodes with a waveform chosen from a number of different waveforms by the user using a control pad on the generating unit. The waveforms have constant amplitude and constant frequency. One problem with the device of PCT Publication No. 94/22529 is that it is difficult to obtain good conductivity between the electrode and the treatment area. Since the electrodes are sewn into the housing, they are not necessarily fixed to the treatment area appropriately even when the housing is correctly worn. The size and shape of the treatment area around which the housing is worn can vary from one user to another and even change shape or size over time. Furthermore, the treatment area itself can change its physical condition as it is repaired. In particular, levels of infection, temperature and pH may vary over time. Thus, a treatment programme chosen for a particular patient when treatment is commenced may need to be varied as treatment progresses. In addition, it has become apparent that supplying alternating current with a simple waveform having constant amplitude and frequency is not necessarily the most effective waveform for encouraging cell regeneration. Accordingly, it is an aim of the present invention to provide an improved device for treating damaged tissue that increases the rate of cell regeneration. It is a further aim of the present invention to provide an improved device for treating damaged tissue that integrates separate elements into a single device that can easily be applied to a treatment area by an uninformed user and which has improved conductivity between the electrodes and the treatment area. It is a still further aim of the present invention to provide an improved device for treating damaged tissue that integrates separate elements into a single device that can easily be applied to a treatment area by an uninformed user and which adapts its programme of treatment according to the physical condition of the treatment area.
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Q: Math brackets in python? Now I'm talking about MATH brackets, not python brackets, I know that parentheses () work like in maths, ex: i = 5*(2+2) print (i) #output = 20 But square brackets [] and curly brackets {} don't work... (I know why they don't work) Thank you, Using Python 3.2.2 A: You don't need "math" brackets -- just use nested parentheses. Humans use [] in writing out complex math expressions to make them more readable to other humans, but this isn't necessary. They don't mean anything different than regular parentheses. So, when writing code, just stick to the parentheses.
3.09375
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New study to test unusual hypothesis on beta brainwaves Beta oscillations are tightly linked to Parkinson's disease and the ability to process sensory information, such as touch. Two neuroscientists have brought their collaboration to Brown University and won funding from the National Science Foundation to see if they can finally provide a definitive, if unorthodox, explanation for beta brainwaves. Before she could seek to convince the world that her computer model of a key brain circuit explains a fundamental, 80-year-old mystery of neuroscience with potential relevance to Parkinson's disease, Stephanie Jones sought to convince Christopher Moore. The new Brown neuroscience professors are now close collaborators, but when they first started talking about the beta oscillations of the cortex, Moore thought Jones was plain wrong, if not a bit nuts. "I was a complete non-believer," he said. "I told her I didn't think this idea could be right." Jones retorted, "Now he's testing the model's predictions." What Jones and Moore now agree upon — and will seek to prove with an $830,000 National Science Foundation grant awarded this month — is that neurons in the cortex experience beta oscillations (cycles of activity at a rate of about 20 times a second) when they receive a combination of two input signals in just the right two places at the right time and with the right strength. The signals, they believe, originate from the distant basal ganglia and reach the cortex by way of the thalamus. The research sounds arcane and technical, but these beta oscillations are powerful and meaningful phenomena that have eluded explanation since they were first detected nearly a century ago. Abnormally strong beta oscillations in the cortex are directly associated with Parkinson's disease. The waves seem to increase as we age, even in healthy people. And when the region of the brain that processes the sense of touch, say in the fingers, is overwhelmed by beta oscillations, the processing doesn't happen. "If you have the beta rhythm in the sensory cortex, our data strongly suggest you will fail at a perceptual task," Moore said, recalling a past human experiment. "You can be sitting here and you tell me you are trying, I know you are trying, you are pushing buttons just like you are trying, but if your cortex happens to show beta right when I tap your finger, you are not going to feel it." Finding an accurate explanation of beta oscillations might not only help explain why the brain's perceptual circuits are wired the way they are, but could also provide doctors with a rational means for improving deep-brain stimulation treatments for Parkinson's disease — and maybe obsessive compulsive disorder — where they apply electrical current to parts of the brain that Moore and Jones suspect of relaying beta signals. "You'd have a mechanistic understanding of why that change [from stimulation] created that change in the circuit," Jones said. One day at lunch ... The two launched their discussion a few years ago in the cafeteria at Massachusetts General Hospital when Moore, then at the Massachusetts Institute of Technology, and Jones, then at the hospital, realized that the circuits he studied in the physical brain were the very ones she modeled in a computer. In particular they shared an interest in a touch-perception circuit, technically known as a "thalamocortical circuit in the somatosensory system." After they began to collaborate, Jones shared that her computational model suggested human data on beta oscillations could best be produced by a delivering a two-signal trigger to neurons in the circuit. One signal comes in at the far end of a neuron where the cell's long branches, or dendrites, extend out. The other, she said, would have to come in at the base of that tree-like structure, where the dendrite extends out from the cell. In neuroscience orthodoxy, no one has ever said that beta oscillations are triggered by such a combination of two signals — but then, orthodoxy has so far failed to explain beta oscillations. Moore had his doubts but experiments began to show indeed that Jones's model, which simulated a circuit of about 300 cells of about five types, predicted what he could observe in real animal brains. In 2009 and 2010 the two began to publish together in the Journal of Neurocience, the Journal of Neurophysiology, and Neuroimage. All the while they puzzled over where these beta-stimulating, two-factor signals could be coming from. Eventually they traced them, at least hypothetically, back to the "non-specific" area of the thalamus and farther back to the basal ganglia. At Brown for the big moment Although each researcher maintains other collaborations, they jumped at the chance to come to Brown last summer. Here they said can collaborate without crossing any bridges and they have access to Brown's computing resources, which can allow Jones's model to expand and run faster. The groundwork of their hypothesis, their increasingly close collaboration, and their access to resources made their first grant application at Brown a success. Now all they have to do is find out if they are right or wrong. As they have always done, Moore will lead the physiological side of things. He'll use optogenetics, a new technology in which scientists engineer brain cells to be turned on or off by flashes of light, to take over the circuits of mice from the basal ganglia to the cortex. He'll be able to see whether turning off particular cells in the basal ganglia, for example, causes beta oscillations in the somatosensory cortex to stop, as the hypothesis and the model would suggest. Meanwhile, Jones will expand the model to incorporate those upstream parts of the brain, the basal ganglia and the thalamus, so that it is more complete. She plans to feed what Moore sees in his experimental results back into the model to refine it as well. The grant runs through the end of October 2014, which should be enough time for Moore and Jones to find out whether they have traced beta oscillations to their neural roots. Moore simultaneously discounts and revels in speculation about what the hypothesis would say about the brain if it is indeed true. Does the basal ganglia, which is implicated in habit formation, use beta oscillations to briefly shut down sensory processing in the cortex so that it can focus the brain on that task of forming habits — which is why Jones wonders whether it could also relate to OCD? If he took control of the beta oscillations in a mouse, could he give the mouse Parkinsonian symptoms and then turn them off at will? For now the implications will have to wait for the more basic step of confirming the hypothesis. Like the beta oscillations themselves, the hypothesis may only come to fruition through a perfect combination of researchers coming together at Brown with perfect timing. Related Stories The research group headed by Professor Atsushi Nambu (The National Institute for Physiological Sciences) and Professor Masahiko Takada (Primate Research Institute, Kyoto University) has shown that the 'oscillatory' nature ... (PhysOrg.com) -- A non-invasive brain imaging technique gives new hope to patients with Parkinson's disease in finding new and better treatment plans and tracking the disease progression, a new University ... Researchers at the University of Pittsburgh have found new evidence that the basal ganglia and the cerebellum, two important areas in the central nervous system, are linked together to form an integrated functional network. ... Recommended for you A team of researchers at the IRCM led by Frédéric Charron, PhD, in collaboration with bioengineers at McGill University, uncovered a new kind of synergy in the development of the nervous system, which explains an important ... Memory loss has recently been associated with excessive silencing of genes through a process called methylation. Researchers at the University of Louisville investigated the effects of a diet rich in methionine—an amino ... (MedicalXpress)—A team of researchers with the University of Maryland and Mt. Sinai School of Medicine has found that brain regions in female rodents associated with sexual behavior are feminized by repression ... Neuroscientists are taking inspiration from natural motor control to design new prosthetic devices that can better replace limb function. In new work, researchers have tested a range of brain-controlled devices ... The decades worth of data that has been collected about the billions of neurons in the brain is astounding. To help scientists make sense of this "brain big data," researchers at Carnegie Mellon University ... User comments Please sign in to add a comment. Registration is free, and takes less than a minute. Read more Click here to reset your password. Sign in to get notified via email when new comments are made.
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The largest genera in Myrsinaceae are the tropical Myrsine (300 species), Ardisia (400-500 species), and Embelia Burman f. (130 species), and the temperate Lysimachia (ca. 160 species). No genera are endemic to the flora area; some species (in Lysimachia) have been introduced and become naturalized. Ardisia elliptica is introduced and has been named a Category I Invasive Species by the Florida Exotic Plant Pest Council (http://www.fleppc.org/list/07list_ctrfld.pdf). Myrsinaceae is of limited economic value, mainly as ornamentals (some Anagallis, Ardisia, Lysimachia). Most taxa are pollinated by insects, particularly bees and flies, with nectar or pollen as rewards; some Lysimachia have oil-secreting hairs and are pollinated by oil-collecting bees (S. Vogel 1974+, vol. 2); selfing also occurs. Temperate seeds are dispersed by gravity, water, wind, or, possibly, ants or other ground-dwelling insects (B. Ståhl and A. A. Anderberg 2004). As circumscribed here, Myrsinaceae are closely related to Primulaceae and Theophrastaceae. M. Källersjö et al. (2000) and B. Ståhl and A. A. Anderberg (2004) removed the nonrosette terrestrial members from Primulaceae and placed them in the Myrsinaceae (see further discussion under Primulaceae). Additional evidence (A. A. Anderberg et al. 2007; L. Martins et al. 2003) indicates that Lysimachia is not monophyletic. Further, Glaux is now considered an apetalous member of Lysimachia (Anderberg et al.; Hao G. et al. 2004); Trientalis probably should be considered an extreme verticillate member of Lysimachia sect. Seleucia (Anderberg et al.; alluded to by J. D. Ray 1956); and some species of Anagallis are more closely related to Lysimachia (Anderberg et al.; M. Källersjö et al. 2000; Anderberg and B. Ståhl 1995) than to other members of Anagallis. More work is still needed to resolve these additional issues. Martins et al. presented nuclear rDNA evidence that Centunculus is basal within Lysimachieae and should not be included within Anagallis but this is not yet fully resolved. The phylogenetic position of Cyclamen, a scapose taxon, has not been resolved; Ståhl and Anderberg (2004) included it in this family because it shares developmental anatomy, leaf pigmentation, and other features. Our understanding of the family is clearly still in flux, and future taxonomic realignments at the familial and generic levels are to be expected.
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Declared a pandemic by the WHO, the world is currently facing the largest health crisis of the last decades. First reported in December 2019 in the Wuhan province of China, the virus SARS-CoV-2 causes the disease COVID-19, ranging from milder flu-like symptoms and fever to severe lung disease and multiple organ failure leading to fatalities. The novel coronavirus shares many similarities with the original Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) which emerged 17 years ago and was extensively studied by the Penninger group at IMBA, who was among the first to describe ACE2 as host cell receptor of the original coronavirus. Recent studies now confirmed that the novel coronavirus SARS-CoV-2 also binds to ACE2 in its host with even higher binding affinity – also explaining the severity of the disease. ACE2 is mainly expressed in the human lung, which is why in most COVID-19 patients, the lungs are heavily affected by the virus. However, ACE2 is also found in additional tissues such as the human heart, kidneys, blood vessels and intestine, which might explain the multiple organ failure oftentimes caused by COVID-19. In the recent study published in Cell, a joint international effort led by Josef Penninger with scientists from Austria, Canada, Sweden and Spain, published groundbreaking results as they were able to slow SARS-CoV-2 viral growth both in cell culture and human organoids. By using a clinical-grade human recombinant soluble ACE2 (hrsACE2) in cell culture, the viral infection was slowed 1000- to 5000-fold. IMBA group leader and founding director Josef Penninger, who is now director of the Life Sciences Institute of the University of British Columbia, explains: “Due to the promising results in vitro, we wanted to test hrsACE2 in vivo – usually, human tests would take years to get the first results. However, we already engineered human capillary organoids at IMBA back in 2019, and in our amazing network of researchers we were able to rapidly generate human kidney organoids. These organoids are a great tool to rapidly develop therapies in COVID-19 disease relevant-human tissue.” These engineered human tissue organoids were infected with SARS-CoV-2 directly purified from a COVID-19 patient and were shown to be able to produce viral progeny in multiple experiments. Following infection with the virus, adding hrsACE2 to the organoids drastically reduced the viral infection, showing the incredible efficiency of the blocking effect. Human recombinant soluble ACE2 (hrsACE2) was developed by the biotech company Apeiron Biologics and has already undergone phase 1 and phase 2 clinical testing in healthy volunteers and patients with lung disease. "We are delighted that this international collaboration, which has been so successful, has produced a solid data base that supports our proposed mode of action for the action of rhACE2, also known as APN01. This of course motivates us all the more to test the efficacy of APN01 in COVID-19 patients in controlled clinical trials," says Peter Llewellyn-Davies, CEO of Apeiron Biologics. Besides blocking the virus, APN01 was designed to protect multiple tissues, especially the lung, from failing. Original publication „Inhibition of SARS-CoV-2 infections in engineered human tissues using clinical-grade soluble human ACE2“, Monteil et al., Cell, 2020; DOI: 10.1016/j.cell.2020.04.004 This study is an international collaboration between the Karolinska Institute and Karolinska University Hospital, the National Veterinary Institute, Uppsala, the Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Technology (BIST), IMBA - Institute of Molecular Biotechnology of the Austrian Academy of Sciences, the company STEMCELL Technologies Inc., Vancouver, Canada, the Center for Applied Medical Research (CIMA), the University of Navarra, Pamplona, Spain, the company Apeiron Biologics, the University of Toronto, the Catalan Institution for Research and Advanced Studies (ICREA), Barcelona, the Centro de Investigación Biomédica en Red en Bioingeniería, Biomateriales y Nanomedicina, Madrid, Spain, as well as the Department of Medical Genetics, Life Science Institute, University of British Columbia, Vancouver, Canada. About IMBA IMBA - Institute of Molecular Biotechnology - is one of the leading biomedical research institutes in Europe focusing on cutting-edge stem cell technologies, functional genomics, and RNA biology. IMBA is located at the Vienna BioCenter, the vibrant cluster of universities, research institutes and biotech companies in Austria. IMBA is a subsidiary of the Austrian Academy of Sciences, the leading national sponsor of non-university academic research. The stem cell and organoid research at IMBA is being funded by the Austrian Federal Ministry of Science and the City of Vienna. About Apeiron Biologics Apeiron Biologics AG is a European private biotechnology company based in Vienna, Austria, specializing in the discovery, development and commercialization of novel immunotherapies for cancer. APN01 is a recombinant human Angiotensin Converting Enzyme 2 (rhACE2) which has already undergone several phase 1 and 2 clinical trials in ARDS (acute respiratory distress syndrome), ALI (acute lung injury) and PAH (pulmonary arterial hypertension). APN01 has been shown to be safe and well tolerated. Recently, ACE2 has been shown to act as a cellular entry receptor for the novel coronavirus SARS-CoV-2. Apeiron is therefore currently preparing a phase 2 clinical trial in Europe for COVID-19 and is exploring options for further clinical development in China. www.apeiron-biologics.com
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Ethanol Ethanol or bioethanol is an alcohol made by fermentation. The most common feedstock is sugar or starch crops. In much of the world the source is corn or sugarcane. Manitoba has an ethanol plant operated by Husky Energy in Minnedosa, Manitoba. The plant feedstock for the facility is non-food feed-grade wheat and corn purchased from local growers. This includes soft wheat, prairie spring wheat, winter wheat and corn. Other grains such as durum, barley, and rye may be used on occasion. Ethanol can be used as a fuel for vehicles in its pure form, but it is usually used as a gasoline additive to increase octane and improve vehicle emissions. Many automobile manufacturers now make alternative fuel vehicles (AFV’s). Available in Canada, they are designed to run on E85 ethanol – 85% ethanol and 15% gasoline. Cellulosic biomass, derived from non-food sources such as trees and grasses, is being developed as a feedstock for ethanol production. Biodiesel Biodiesel is made from vegetable oils and animal fats using a process called transesterification. Biodiesel can be used alone as a fuel for vehicles in its pure form, but it is usually used as a diesel additive to reduce levels of particulates, carbon monoxide, and hydrocarbon emissions. Research indicates that 20% biodiesel to 80% conventional diesel is the best mixture for reducing emissions and engine wear, while maximizing performance. However, in Manitoba lower concentrations are usually called for to reduce problems of gelling in cold temperatures. In 2009, Manitoba became the first province in Canada to mandate the use of biodiesel. As of November 1, 2009 all diesel fuel sold in the province must contain an average of two percent biodiesel. Biodiesel has low aquatic toxicity and biodegrades in 30 days, making it an excellent alternative fuel choice for boats. Natural Gas Natural Gas is a fossil fuel that consists of 90% methane. Emissions from natural gas vehicles (NGV) are mostly unburned methane. As such, it does not contribute to the formation of photochemical pollution (smog). Methane is also a greenhouse gas, but well-maintained NGV’s release fewer total emissions because of fuel system design. Propane Propane or liquified petroleum gas (LPG) consists mainly of propane, propylene, butane and butylene in various mixtures (1). Much of Winnipeg’s taxi fleet operated on propane before they converted to hybrid vehicles. It is the most publicly accessible alternative fuel.
3.265625
3
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Henschel Hs 117 The Henschel Hs 117 Schmetterling (German for Butterfly) was a radio-guided German surface-to-air missile project developed during World War II. There was also an air-to-air version, the Hs 117H. The operators used a telescopic sight and a joystick to guide the missile by radio control, which was detonated by acoustic and photoelectric proximity fuses, at . Development In 1941, Professor Herbert A. Wagner (who was previously responsible for the Henschel Hs 293 anti-ship missile) invented the Schmetterling missile and submitted it to the Reich Air Ministry (RLM), who rejected the design because there was no need for more anti-aircraft weaponry. However, by 1943 the large-scale bombing of Germany caused the RLM to change its mind, and Henschel was given a contract to develop and manufacture it. The team was led by Professor Wagner, and it produced a weapon somewhat resembling a bottlenose dolphin with swept wings and cruciform tail. In May 1944, 59 Hs 117 missiles were tested, some from beneath a Heinkel He 111; over half the trials failed. Mass production was ordered in December 1944, with deployment to start in March 1945. Operational missiles were to be launched from a 37mm gun carriage. In January 1945, a prototype for mass production was completed, and production of 3,000 missiles a month was anticipated, but on 6 February, SS-Obergruppenführer Hans Kammler cancelled the project. Variants The Hs 117H was an air-launched variant, designed to be launched from a Dornier Do 217, Junkers Ju 188, or Junkers Ju 388. This version was designed to attack enemy aircraft up to above the launching aircraft. See also References External links Henschel Hs117 Schmettering (Butterfly) - Royal Air Force Museum, Cosford (UK) German language page on the Hs 117 Schmetterling SAM missile Category:World War II guided missiles of Germany Category:Surface-to-air missiles of Germany
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Millions of people living along the Mekong River face a possibly irreversible depletion of key food supplies resulting from dam building and other diversions of its waters. Deforestation upstream along the riverbanks and poor land and water use practices in Vietnam’s downstream Mekong Delta have added to what can only be called a looming crisis. The Mekong is Southeast Asia’s longest river, with 60 to 70 million people depending on it for food, commerce, irrigation, transportation, and drinking water. But the river’s slowly developing crisis rarely gains much attention from mainstream Western media. This is partly because of a lack of transparency from regional governments and developers over plans by China, Laos, and Cambodia to build more dams. It’s not easy to obtain hard data on the dam projects. And the Mekong River Commission (MRC), a regionally based international body which is supposed to help manage and contain threats to the river, has proven to be ineffective except when it comes to producing research reports. The reports have been useful in raising awareness among experts and nongovernmental organizations focused on protecting the environment. But the MRC has no authority to enforce its recommendations. In late May, the Cambodia-based Phnom Penh Post reported that frustrated donors are turning away from the commission, with the MRC “losing more than half its funds and employees.” The MRC is “becoming all but irrelevant,” the paper’s correspondent reported. Impact in Laos and Cambodia Just to the south of China’s Yunnan Province dams, Laos is already feeling the dams’ impact. Laotian fishermen have been complaining for several years about lower water levels in the Mekong and a drop in their fish catch. This is partly due to the loss of fish moving south that are blocked and ground up by the dams’ turbines. The dams also block adult fish trying to migrate upstream, and stop larvae and juveniles trying to swim downstream. And dams trap sediment needed to enrich the soil in the riverbed and downstream lakes and tributaries. When it comes to Laos, China’s example has not been helpful. “China’s construction of hydropower projects on the upper Mekong River…has shown Laos that it can ignore protests from downstream countries about the negative effects of its dams,” says Brian Eyler, deputy director of the Southeast Asia program at the Stimson Center in Washington, D.C. Eric Baran, a marine biologist based in Phnom Penh for the WorldFish Institute, estimates that some 60 percent of the population in Laos and Cambodia rely on fish for their entire daily protein consumption. The Mekong dams in Laos could cut off natural migratory patterns of more than 110 fish species, Baran says. In northeastern Cambodia, the Lower Sesan 2 dam, still under construction, has already reduced the fish catch of villagers in the area. This has triggered widespread protests from villagers who are being displaced due to the inundation of villages upstream from the dam. Thousands of people, many of them from ethnic minority groups, are expected to lose most of their fish resources because of the dam’s blocking of fish migrating from the Mekong and Sekong Rivers. Ian Baird, an expert on the impact of dams in Southeast Asia at the University of Wisconsin, estimates that at least 78,000 people living above the Sesan 2 dam site will lose their access to migratory fish. Baird told Radio Free Asia that on a broader scale “hundreds of thousands of people, or even millions, stand to be impacted in Cambodia and Vietnam as well as in Laos and Thailand, since fish migrations will be affected there.” The role of Thailand is sometimes overlooked in the development of the Mekong River dams. Chinese, Malaysian, and Thai companies are leading developers of the dams in Laos. And Thai banks finance some of the projects. The Mekong Delta In Vietnam’s Mekong Delta, a combination of drought, climate change, the effects of the El Nino phenomenon, and the impact of upstream Chinese dams is devastating rice crops. The Delta, home to some 18 million people, is one of the world’s leading rice exporters. A Vietnamese government “rice first” policy dating back to the mid-1970s that has encouraged farmers to grow three crops of rice per year has turned out to be counterproductive. Farmers complain, meanwhile, that the dams have greatly reduced the amount of silt, or sediment, that once reached the Delta. Silt helped to form the Mekong Delta over thousands of years. The loss of silt and rising sea levels have now resulted in salt water reaching nearly 40 miles into the Delta. Some farmers have coped by raising shrimp in the briny water. But a reduction in rice exports now means a drop of income for many. What's next for the Mekong? On a more positive note, Richard Cronin and Courtney Weatherby argued in a Stimson Center report in October last year that a combination of factors could lead to less dam building. These factors would include “rising political and financial risks and changing global energy prices” as well as a “new interest from donor governments and institutions in identifying alternatives to destructive mainstream dams…” “The possibility that not all of the planned dams may go forward,” the authors of the report say, “opens up a new opportunity for Laos to reconsider its current commitment to all nine of its planned Mekong dams.” The Lao government wants to use its hydropower for electric power exports to other countries, such as neighboring Thailand. Its aim is to become the “battery of Southeast Asia.” But a preliminary study by the Asian Development Bank (ADB) found that if Laos can upgrade older dams on tributaries of the Mekong and link them with a national grid, this will give Laos the short-term revenues it seeks without further disrupting the river. “Another China-related factor that may be critical to the viability of dams on the mainstream and major tributaries is the question of future water availability,” says the Stimson report. The Mekong has its origins in Tibet. “As climate change melts Himalayan glaciers and changes patterns, scientists are questioning the long-term utility of dams that depend on regular flows to operate during the dry season,” the report says. “Should increasingly water-stressed China prioritize other uses of water in the Upper Mekong over electricity production," the report adds, "the planned mainstream dams in the Lower Mekong might not receive enough water to operate during the driest three or four months of the year." This is when flows from China are the region's most important source of water, the report says.
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Q: Time calculation with negative value results Java I want to calculate the difference between a start time and an end time. In HH:mm format. I receive a negative value when, for example, the start time is 22.00 and the end time is 1.00 the next day. How do I let the program know the end time is on the next day? My script: public void setBeginTijd() { String dateStart = "22:00"; String dateEnd = "1:00"; SimpleDateFormat format = new SimpleDateFormat("HH:mm"); Date d1 = null; Date d2 = null; try { d1 = format.parse(dateStart); d2 = format.parse(dateEnd); long diff = d2.getTime() - d1.getTime(); long diffMinutes = diff / (60 * 1000) % 60; long diffHours = diff / (60 * 60 * 1000) % 24; System.out.println(diffMinutes); System.out.println(diffHours); } catch (Exception e) { e.printStackTrace(); } } A: If you can assume that, when the time is negative, the second time must be on the next day, then you can simply say if (diff < 0) { diff = (24 * 60 * 60 * 1000) + diff; } EDIT to elaborate this, also in response to the comments: Of course this is a very simplistic solution. It can not handle the case where the second date is two days later. It does not handle DST switches. It does not handle the time zone change on December 31st, 1927 in Shanghai. It is no replacement for a properly modelled date with all its caveats. It is a best-effort approach to derive what can (probably) be derived from the given information. A: As already mentioned by some people, it is important to also know day, month and year of each event to calculate periods for events that are not on the same day. I modified your method the way I think it could help you: public void setBeginTijd() { String dateStart = "22.08.2014 22:00"; String dateEnd = "25.08.2014 01:00"; SimpleDateFormat fullFormat = new SimpleDateFormat("dd.MM.yyyy HH:mm"); Date d1 = null; Date d2 = null; try { d1 = fullFormat.parse(dateStart); d2 = fullFormat.parse(dateEnd); long diff = d2.getTime() - d1.getTime(); long diffMinutes = diff / (60 * 1000) % 60; long diffHours = diff / (60 * 60 * 1000) % 24; long diffDays = diff / (24 * 60 * 60 * 1000); System.out.println("Delta minutes: " + diffMinutes); System.out.println("Delta hours: " + diffHours); System.out.println("Delta days: " + diffDays); } catch (Exception e) { e.printStackTrace(); } }
3.234375
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There are many different types of tumors and cancers. Gliomas are the most common type of primary brain tumors and are thought to arise from glial cells, or precursors of glial cells, that surround, support, and cooperatively interact with neurons in the brain. Because gliomas generally have already extensively invaded brain tissue before a patient is aware of the disease, gliomas are generally not curable. Glioblastomas are the most malignant and most commonly occurring type of gliomas in adults, representing about 50 percent of all gliomas. Glioblastomas are distinguished by necrosis, or tissue death, within the central portion of the tumor or irregularly spaced between vascular tissues, and by a surrounding shell of tissue diffusely invaded by peripheral tumor cells and characterized by edema. The aggressive behavior of glioblastomas is reflected in the nearly 100 percent fatality rate of patients suffering from this type of tumor within approximately two years following diagnosis, even after extensive medical intervention, including surgery, radiotherapy, and chemotherapy. Despite continual advancements in imaging technologies, glioma cells generally invade far beyond the regions recognized as being abnormal using various types of clinical imaging technologies, including computer-aided tomography (“CT”), magnetic-resonance imaging (“MRI”), and positron emission tomography (“PET”). The extent of glioma-cell invasion is generally greater than that assumed for current radiotherapy-treatment planning. Currently, an additional shell of tissue invaded by glioma cells, having a thickness of approximately two centimeters, is assumed to surround the volume of the tumor seen in CT, MRI, or PET images. Because the extent of glioma-cell invasion is currently inaccurately modeled, therapies based on understanding the extent of glioma-cell invasion are often misapplied, leaving certain of the glioma cells that have diffused away from the tumor mass untreated or inadequately treated. The medical community continues to seek improved methodologies for characterizing both the extent of glioblastomas and other tumors as well as determining the aggressiveness of tumors and additionally characterizing the tumors in order to guide medical interventions as well as provide accurate prognoses for patients.
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A new study appears to shed more light on the harmful effects of smoking while pregnant using 4D ultrasound scans to detect the tiny movements made by foetus in the womb. By monitoring the growing babies, scientists believe that they can flag potential problems by examining the minute movements foetuses make in the womb. It is hoped that the research can be used to encourage more mothers to give up the habit while pregnant. The top set of images show the baby in a womb of a smoking mother, compared to one whose mother was not a smoker (PA) Dr Nadja Reissland studied the moving 4D ultrasound scans of 20 expectant mothers, four of whom were smokers, recording thousands of tiny movements as the foetuses developed at 24, 28, 32 and 36 weeks. Her study, conducted at the James Cook University Hospital in Middlesbrough, found that the unborn babies of the four smoking mothers touched their faces more frequently. Foetuses usually move their mouths and touch themselves as they develop and gain control over their limbs. Dr Reissland’s results – which she hopes to replicate across a far larger sample size – indicates that mothers who smoke may delay the development of their babies’ central nervous systems. “A larger study is needed to confirm these results and to investigate specific effects, including the interaction of maternal stress and smoking,” Dr Reissland said. Although the number of women smoking during pregnancy has fallen to an all-time low, according to figures gathered last year, 12 per cent of expectant mothers continue smoking. However, figures vary across the country. In 2013-2014, 28 per cent of pregnant women who attended the NHS Blackpool smoked, while in central London only two per cent of expectant mothers smoked. Research has found that pregnant mothers who smoke risk damaging their unborn children’s hearts and can also increase the risk of miscarriage and premature births. The scans show differences in movement ebtween foetuses of smoking and non-smoking mothers (PA) The pilot study, conducted by Durham and Lancaster Universities, was published in the medical journal Acta Paediatrica. Dr Reissland, who specialises in foetal development, called for women to be offered more help in giving up, rather than demonising those mothers who smoke. "I'm really grateful, they did a good thing," she said. "These are special people and they overcame the stigma to help others."
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Q: Why do we need torque separately from force? I'm studying physics for a couple of month now and and I am currently finding it a bit unsatisfying how the basic physical concepts are presented, meaning often times we only get a formula ($\tau=r \times F$, for example) without much discussion or any derivation. So I was trying to build up a bit of background knowledge and intuition from the Feynman lectures. From what I understand he derived torque (firstly without vectors) simply by inserting angular coordinates into the displacement in the work formula and rearranged it: \begin{equation} \Delta W=F_x\,\Delta x+F_y\,\Delta y. \end{equation} angular coordinates ("angular displacement"?): \begin{equation} \Delta x=-PQ\sin\theta=-r\,\Delta\theta\cdot(y/r)=-y\,\Delta\theta. \end{equation} \begin{equation} \Delta y=+x\,\Delta\theta. \end{equation} inserted: \begin{equation} \Delta W=(xF_y-yF_x)\Delta\theta. \end{equation} He then calls the part without the angle "torque". So isn't the torque just a special kind of force, one that acts on a circular displacement? Why do we treat force and torque so seperately when torque just seems to emerge when we work with angular coordinates? Isn't this just a special case, why can't we not use just force all the time (and not separate force/momentum/... and torque/angular momentum/... so strictly)? Obviously I'm thinking about it the wrong way and have some major misunderstandings regarding the concept of torque and thus angular momentum etc. Are there any "better"/other derivations of this concept? After weeks of frustration I signed up here, maybe you have a better way of getting some intuition with torque. Thanks. A: That derivation of Feynman's is one of the best around. As you have worked out yourself, in principle you can think of everything in terms of force as long as you also know the position vector where the force acts. This is actually more information - often a great deal more - than you need to compute the dynamics and statics of a rigid body: you can slide a force vector along the straight line with its same direction and passing through its tail, and the effect of that force on a rigid body's dynamics is the same (although where the force acts is important for working out internal stresses on a body). The sum of forces acting at the centre of mass and the nett torque about the centre of mass is all the information you need to compute rigid body statics and dynamics. This is in general a great deal less information (three vectors: force, torque and position of centre of mass) than a specification of all the individual forces and their positions of action. So, if you like, this is an instance of data compression to make a description of dynamics more wieldy. Another way of thinking of the split between force and torque is that they correspond to the natural, intuitive split between the Euclidean isometries of translation and rotation. Feynman's work calculation is splitting the work done by a system of forces into the resulting translational kinetic energy that results and the kinetic energy associated with rotation about the centre of mass. Ultimately you will meet the notion of Lagrangian dynamics and Noether's Theorem. Feynman from memory touches on these notions in his famous lectures in a "Symmetry In Physics" chapter. From Noether's Theorem we understand that the conservation of various quantities arises because our description of physics does not change if we impart continuous transformations on our co-ordinate systems: because most physics does not change if we shift our time co-ordinate origin, we conclude through Noether's theorem that there is a conserved quantity which we call energy. Conservation of momentum arises because our physics is invariant with respect to translations of our co-ordinate systems (one component of momentum conservation for each component of co-ordinate translation) and conservation of angular momentum arises because our physics is invariant with respect to co-ordinate translations. So again we see a split of conserved quantities between those to do with translation (momentum) and those to do with rotation (angular momentum). The split thus arises very neatly and naturally from the notions of Eucledean isometries.
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Caught on camera https://creativecommons.org/licenses/by-nc-sa/3.0/ Computers are playing spot the difference in the Serengeti. An image-recognition algorithm that can identify different species could make it easier to track animals in the wild. Using a database of 3.2 million photos taken by hidden camera traps in the Serengeti National Park in Tanzania, Jeff Clune at the University of Wyoming in Laramie and his colleagues trained the deep-learning system to distinguish between 48 animal species, such as elephants, giraffes and gazelles. In tests, it correctly identified the species present in an image 92 per cent of the time. Camera traps automatically take pictures of passing animals when triggered by heat and motion. This produces thousands or millions of photographs for ecologists to study, but people usually have to go through and label what each picture shows by hand, says Ali Swanson, who worked on the project while at the University of Oxford. If an algorithm could categorise at least some of the images, it could save a lot of time. In 2010, Swanson set up 225 camera traps in the Serengeti, inviting an army of 70,000 online volunteers to help label the images. When Clune heard about this, he saw a perfect opportunity for deep learning – so he and Swanson arranged to team up on the project. “Right now in AI and deep learning, one of the hardest things to come by is a very good, large labelled dataset,” says Clune. His team started by teaching a neural network to recognise whether an image contained an animal, which 75 per cent of the Serengeti images lack. The researchers then trained it to differentiate between species. Better ID The system is much better at identifying the most common animals in the data set, such as wildebeest, says Clune. It has trouble with more rare species like the zorilla, a type of polecat that only appears in the images a few dozen times. Clune says the system could be used to classify most of the photographs and researchers could work on any it wasn’t sure about. It could then be further trained on these hand-labelled images to get better at recognising rarer species. The team also plans to test whether the system can identify animal behaviour in images. “This is very exciting,” says Chris Carbone at the Zoological Society of London. Automatic species recognition could help us learn more about the distribution of species and get a better idea of the impact humans are having on them, he says. An ideal system would provide live tracking information about animals as they pass traps, says Swanson. But the challenge would be transmitting the data from the device in real time for the system to analyse, rather than the current method of using an SD card to store the data on the device until a researcher comes along to collect it. One difficulty is that hyenas and elephants have a habit of damaging the cameras, which are thus kept in heavy-duty plastic cases with no space for an antenna that can transmit data. “And if you do put an antenna on a camera, it won’t last very long at all,” says Swanson. “Something will come along and chew it off pretty quick.” Reference: arxiv.org/abs/1703.05830
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Q: How to find if a number is a subset of a given integer in Python I am writing a program with python to find if a number is present as a set in another number for example: if the number, a = '123456789010234 and I have to find if '4567' is present in a or not. A: Try using in, if both are integers: str(num) in str(a) >>> a = 123456789010234 >>> num = 4567 >>> str(num) in str(a) True
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Q: Fluorine isotopes and isomers I was looking up fluorine isotopes out of curiosity. The Wikipedia entry gives info on them but adds there are also two isomers which are $\mathrm{^{18m}F}$ and $\mathrm{^{26m}F}$. What is an isomer of an atomic nucleus please someone? A: Just like electrons nuclei can exist in a number of quantised states. We see evidence of this when, during radioactive decay, a gamma ray is produced. This is a nucleus in an excited state decaying to the ground state, and the excess energy being radiated away as a gamma ray photon. This is precisely analogous to an electron in an atom falling from a high energy state to a lower energy one, and thus producing radiation which we can see in an atomic spectrum. So an isomer of a nucleus is simply that nucleus in a state which is not the ground (lowest energy) state. Most isomers are very short lived, and thus the gamma radiation appears to be more or less coincident with any other radiation that is produced during a radioactive decay. For instance the $\ce{^{18m}F}$ isomer you mention has a lifetime of 162ns according to https://en.wikipedia.org/wiki/Isotopes_of_fluorine . However the odd one is much longer lived, and for a remarkable case of one that is observationally stable take a look at $\ce{^{180m}Ta}$. 0.012% of natural Tantalum consists of this isomer, and it has never been observed to decay to the ground state - as is usual in such cases symmetry forbids the transition. And what I find even more remarkable is that the ground state itself is unstable with respect to both electron capture and beta emission, decaying to isotopes of Hafnium and Tungsten with a half life of just over 8 hours! See https://en.wikipedia.org/wiki/Isotopes_of_tantalum for details. Sorry - slightly belated edit, but it occurred to me that isomers do have one very direct use in Chemistry, namely Mossabuer spectroscopy, see https://en.wikipedia.org/wiki/M%C3%B6ssbauer_spectroscopy. In essence very small changes in the energy of the gamma ray that is emitted when the isomer decays to the ground state can be detected by this technique, and can be related to changes in the chemical environment within which the atom finds itself.
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