1,041 research outputs found

    Analysis of Two-Body Decays of Charmed Baryons Using the Quark-Diagram Scheme

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    We give a general formulation of the quark-diagram scheme for the nonleptonic weak decays of baryons. We apply it to all the decays of the antitriplet and sextet charmed baryons and express their decay amplitudes in terms of the quark-diagram amplitudes. We have also given parametrizations for the effects of final-state interactions. For SU(3) violation effects, we only parametrize those in the horizontal WW-loop quark diagrams whose contributions are solely due to SU(3)-violation effects. In the absence of all these effects, there are many relations among various decay modes. Some of the relations are valid even in the presence of final-state interactions when each decay amplitude in the relation contains only a single phase shift. All these relations provide useful frameworks to compare with future experiments and to find out the effects of final-state interactions and SU(3) symmetry violations.Comment: 28 pages, 20 Tables in landscape form, 4 figures. Main changes are: (i) some errors in the Tables and in the relations between the quark-diagram amplitudes of this paper and those of Ref.[10] are corrected, (ii) improvements are made in the presentation so that comparisons with previous works and what have been done to include SU(3) breaking and final-state interactions are more clearly stated; to appear in the Physical Review

    Nonfactorization in Hadronic Two-body Cabibbo-favored decays of D^0 and D^+

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    With the inclusion of nonfactorized amplitudes in a scheme with Nc=3N_c=3, we have studied Cabibbo-favored decays of D0D^0 and D+D^+ into two-body hadronic states involving two isospins in the final state. We have shown that it is possible to understand the measured branching ratios and determined the sizes and signs of nonfactorized amplitudes required.Comment: 15 pages, Late

    Metabolic Characterization of the Common Marmoset (Callithrix jacchus)

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    High-resolution metabolomics has created opportunity to integrate nutrition and metabolism into genetic studies to improve understanding of the diverse radiation of primate species. At present, however, there is very little information to help guide experimental design for study of wild populations. In a previous non-targeted metabolomics study of common marmosets (Callithrix jacchus), Rhesus macaques, humans, and four non-primate mammalian species, we found that essential amino acids (AA) and other central metabolites had interspecies variation similar to intraspecies variation while non-essential AA, environmental chemicals and catabolic waste products had greater interspecies variation. The present study was designed to test whether 55 plasma metabolites, including both nutritionally essential and non-essential metabolites and catabolic products, differ in concentration in common marmosets and humans. Significant differences were present for more than half of the metabolites analyzed and included AA, vitamins and central lipid metabolites, as well as for catabolic products of AA, nucleotides, energy metabolism and heme. Three environmental chemicals were present at low nanomolar concentrations but did not differ between species. Sex and age differences in marmosets were present for AA and nucleotide metabolism and warrant additional study. Overall, the results suggest that quantitative, targeted metabolomics can provide a useful complement to non-targeted metabolomics for studies of diet and environment interactions in primate evolution.National Institutes of Health (U.S.) (grant AG038746

    Weak radiative hyperon decays, Hara's theorem and the diquark

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    Weak radiative hyperon decays are discussed in the diquark-level approach. It is pointed out that in the general diquark formalism one may reproduce the experimentally suggested pattern of asymmetries, while maintaining Hara's theorem in the SU(3) limit. At present, however, no detailed quark-based model of parity-violating diquark-photon coupling exists that would have the necessary properties.Comment: 10 pages, LaTe

    Sex differentiation in grayling (Salmonidae) goes through an all-male stage and is delayed in genetic males who instead grow faster.

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    Fish populations can be threatened by distorted sex ratios that arise during sex differentiation. Here we describe sex differentiation in a wild grayling (Thymallus thymallus) population that suffers from distorted sex ratios. We verified that sex determination is linked to the sex determining locus (sdY) of salmonids. This allowed us to study sex-specific gene expression and gonadal development. Sex-specific gene expression could be observed during embryogenesis and was strong around hatching. About half of the fish showed immature testes around eleven weeks after fertilization. This phenotype was mostly replaced by the "testis-to-ovary" or "ovaries" phenotypes during development. The gonads of the remaining fish stayed undifferentiated until six months after fertilization. Genetic sexing revealed that fish with undifferentiated gonads were all males, who grew larger than the genetic females during the observational period. Only 12% of the genetic males showed testicular tissue six months after fertilization. We conclude that sex differentiation starts before hatching, goes through an all-male stage for both sexes (which represents a rare case of "undifferentiated" gonochoristic species that usually go through an all-female stage), and is delayed in males. During these juvenile stages males grow faster than females instead of developing their gonads

    Two-body Cabibbo-suppressed Decays of Charmed Baryons into Vector Mesons and into Photons

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    The heavy quark effective theory and the factorization approximation are used to treat the Cabibbo-suppressed decays of charmed baryons to vector mesons, ΛCpρ0,pω\Lambda_C\rightarrow p{\rho^0}, p\omega, ΞC+,0Σ+,0ϕ,Σ+,0ρ0,Σ+,0ω\Xi_C^{+,0}\rightarrow\Sigma^{+,0}\phi, \Sigma^{+,0}{\rho^0}, \Sigma^{+,0}\omega and ΞC0Λϕ,Λρ,Λω\Xi_C^{0}\rightarrow\Lambda\phi, \Lambda\rho, \Lambda\omega. The input from two recent experimental results on ΛC\Lambda_C decays allows the estimation of the branching ratios for these modes, which turn out to be between 10410^{-4} and 10310^{-3}. The long distance contribution of these transitions via vector meson dominance to the radiative weak processes ΛCpγ\Lambda_C\rightarrow p\gamma, ΞCΣγ\Xi_C\rightarrow\Sigma\gamma and ΞC0Λγ\Xi_C^0\rightarrow\Lambda\gamma leads to quite small branching ratios, 10610910^{-6}-10^{-9}; the larger value holds if a sum rule between the coupling constants of the vector mesons is broken.Comment: 11 pages, latex, no figure

    2,2,2-Trifluoroethoxy Derivatives of Chromium(III): Synthesis & Coordination Chemistry

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    214-21

    Dynamics of coherently pumped lasers with linearly polarized pump and generated fields

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    The influence of light polarization on the dynamics of an optically pumped single-mode laser with a homogeneously broadened four-level medium is theoretically investigated in detail. Pump and laser fields with either parallel or crossed linear polarizations are considered, as are typical in far-infrared-laser experiments. Numerical simulations reveal dramatically different dynamic behaviors for these two polarization configurations. The analysis of the model equations allows us to find the physical origin of both behaviors. In particular, the crossed-polarization configuration is shown to be effective in decoupling the pump and laser fields, thus allowing for the appearance of Lorenz-type dynamics

    Study of the decay asymmetry parameter and CP violation parameter in the Lambdac+ --> Lambda pi+ decay

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    Using data from the FOCUS (E831) experiment at Fermilab, we present a new measurement of the weak decay-asymmetry parameter alpha(Lambdac) in Lambdac --> Lambda pi decay. Comparing particle with antiparticle decays, we obtain the first measurement of the CP violation parameter : A = [alpha(Lambdac)+alpha(antiLambda_c)]/[alpha(Lambdac)-alpha(antiLambda_c)]. We obtain alpha(Lambdac)=-0.78+-0.16+-0.13 and A = -0.07+-0.19+-0.12 where errors are statistical and systematic.Comment: 18 pages, to be submitted to Phys. Lett. B For a list of the FOCUS collaboration, see http://www-focus.fnal.gov/authors.htm
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