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A geometrical method for computing overlap between vowel distributions, the spectral overlap assessment metric (SOAM), is applied to an investigation of spectral (F1, F2) and temporal (duration) relations in three different types of systems: one claimed to exhibit primary quality (American English), one primary quantity (Jamaican Creole), and one about which no claims have been made (Jamaican English). Shapes, orientations, and proximities of pairs of vowel distributions involved in phonological oppositions are modeled using best-fit ellipses (in F1 x F2 space) and ellipsoids (F1 x F2 x duration). Overlap fractions computed for each pair suggest that spectral and temporal features interact differently in the three varieties and oppositions. Under a two-dimensional analysis, two of three American English oppositions show no overlap; the third shows partial overlap. All Jamaican Creole oppositions exhibit complete overlap when F1 and F2 alone are modeled, but no or partial overlap with incorporation of a factor for duration. Jamaican English three-dimensional overlap fractions resemble two-dimensional results for American English. A multidimensional analysis tool such as SOAM appears to provide a more objective basis for simultaneously investigating spectral and temporal relations within vowel systems. Normalization methods and the SOAM method are described in an extended appendix.  相似文献   
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The presence of tellurium in copper–nickel sulfide ores results in downstream contamination of leach solutions and electrolytes. Tellurium must be removed from leach solutions before electrowinning to prevent contamination of copper cathodes. Cuprous ion is industrially used as a reductant to remove tellurium ions. However, the reduction kinetics of tellurium ions with cuprous is not well known. In this study, the slow TeVI reduction step with cuprous was identified and a plausible TeVI reduction mechanism was suggested. The rate‐determining step was investigated by studying the kinetics of the coupled reaction of TeVI and TeIV with cuprous. The rate law suggested for the reduction of TeIV with cuprous and the coupled kinetics equation for consecutive reduction reactions of TeIV and TeVI were derived. It was shown that the rate constant of the coupled reaction is very close to the rate constant calculated based on the assumption that TeVI reduction is a rate‐determining step.  相似文献   
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Previous studies have shown that the natural radioactivity contained in building materials have significantly influenced the dose rates in dwelling. Exposure to natural radiation in building has been of concerned since almost 80 % of our daily live are spend indoor. Thus, the aim of the study is to assess the radiological risk associated by natural radioactivity in soil based building materials to dwellers. A total of 13 Portland cement, 46 sand and 43 gravel samples obtained from manufacturers or bought directly from local hardware stores in Peninsular of Malaysia were analysed for their radioactivity concentrations. The activity concentrations of 226Ra, 232Th and 40K in the studied building materials samples were found to be in the range of 3.7–359.3, 2.0–370.8 and 10.3–1,949.5 Bq kg?1 respectively. The annual radiation dose rates (μSv year?1) received by dwellers were evaluated for 1 to 50 years of exposure using Resrad-Build Computer Code based on the activity concentration of 226Ra, 232Th and 40K found in the studied building material samples. The rooms modelling were based on the changing parameters of concrete wall thickness and the room dimensions. The annual radiation dose rates to dwellers were found to increase annually over a period of 50 years. The concrete thicknesses were found to have significantly influenced the dose rates in building. The self-absorption occurred when the concrete thickness was thicker than 0.4 m. Results of this study shows that the dose rates received by the dwellers of the building are proportional to the size of the room. In general the study concludes that concrete building materials; Portland cements, sands, and gravels in Peninsular of Malaysia does not pose radiological hazard to the building dwellers.  相似文献   
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Zeaxanthin carotenoids are class of commercially important natural products and diverse biomolecules produced by plants and many microorganisms. Bacteria often produce a cocktail of polar and nonpolar carotenoids limiting their industrial applications. Marine members of the family Flavobacteriaceae are known to produce potential carotenoids such as astaxanthin and zeaxanthin. A few bacterial species have been reported for the predominant production zeaxanthin. Here, we report the molecular identification of the zeaxanthin as a major carotenoid produced by two novel bacteria (YUAB-SO-11 and YUAB-SO-45) isolated from sandy beaches of South West Coast of India and the effect of carbon sources on the production of zeaxanthin. The strains were identified based on the 16S rRNA gene sequencing as a member of genus Muricauda. The closest relatives of YUAB-SO-11 and YUAB-SO-45 were Muricauda aquimarina (JCM 11811T) (98.9 %) and Muricauda olearia (JCM 15563T) (99.2 %), respectively, indicating that both of these strains might represent a novel species. The highest level of zeaxanthin production was achieved (YUAB-SO-11, 1.20?±?0.11 mg g?1) and (YUAB-SO-45, 1.02?±?0.13 mg g?1) when cultivated in marine broth supplemented with 2 % NaCl (pH 7) and incubated at 30 °C. Addition of 0.1 M glutamic acid, an intermediate of citric acid cycle, enhanced the zeaxanthin production as 18 and 14 % by the strains YUAB-SO-11 and YUAB-SO-45 respectively. The zeaxanthin showed in vitro nitric oxide scavenging, inhibition of lipid peroxidation, and 2,2-diphenyl-1-picryl hydrazyl scavenging activities higher than the commercial zeaxanthin. The results of this study suggest that two novel strains YUAB-SO-11 and YUAB-SO-45 belonging to genus Muricauda produce zeaxanthin as a predominant carotenoid, and higher production of zeaxanthin was achieved on glutamic acid supplementation. The pigment showed good in vitro antioxidant activity, which can be exploited further for commercial applications.  相似文献   
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We present a method that significantly enhances the robustness of (automated) NMR structure determination by allowing the NOE data corresponding to unassigned NMR resonances to be used directly in the calculations. The unassigned resonances are represented by additional atoms or groups of atoms that have no interaction with the regular protein atoms except through distance restraints. These so-called "proxy" residues can be used to generate NOE-based distance restraints in a similar fashion as for the assigned part of the protein. If sufficient NOE information is available, the restraints are expected to place the proxies at positions close to the correct atoms for the unassigned resonance, which can facilitate subsequent assignment. Convergence can be further improved by supplying additional information about the possible identities of the unassigned resonances. We have implemented this approach in the widely used automated assignment and structure calculation protocols ARIA and CANDID. We find that it significantly increases the robustness of structure calculations with regard to missing assignments and yields structures of higher quality. Our approach is still able to find correctly folded structures with up to 30% randomly missing resonance assignments, and even when only backbone and beta resonances are present! This should be of significant value to NMR-based structural proteomics initiatives.  相似文献   
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The single-domain GH11 glycosidase from Bacillus circulans (BCX) is involved in the degradation of hemicellulose, which is one of the most abundant renewable biomaterials in nature. We demonstrate that BCX in solution undergoes minimal structural changes during turnover. NMR spectroscopy results show that the rigid protein matrix provides a frame for fast substrate binding in multiple conformations, accompanied by slow conversion, which is attributed to an enzyme-induced substrate distortion. A model is proposed in which the rigid enzyme takes advantage of substrate flexibility to induce a conformation that facilitates the acyl formation step of the hydrolysis reaction.  相似文献   
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We compare the results of small angle neutron scattering on the flux line lattice (FLL) obtained in the borocarbide superconductor LuNi2B2C with the applied field along the c- and a-axes. For H‖c the temperature dependence of the FLL structural phase transition from square to hexagonal symmetry was investigated. Above 10 K the transition onset field. H 2(T), rises sharply, bending away from H c2(T) in contradiction to theoretical predictions of the two merging. For H‖a a first order FLL reorientation transition is observed at H tr=3–3.5 kOe. Below H tr the FLL nearest neighbor direction is parallel to the b-axis, and above H tr to the c-axis. This transition cannot be explained using nonlocal corrections to the London model.  相似文献   
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