4,527 research outputs found

    Generalised CP and A4 family symmetry

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    We perform a comprehensive study of family symmetry models based on A4 combined with the generalised CP symmetry H CP. We investigate the lepton mixing parameters which can be obtained from the original symmetry A4 ? H CP breaking to different remnant symmetries in the neutrino and charged lepton sectors. We find that only one case is phenomenologically viable, namely G?CP?ZS2×H?CP in the neutrino sector and GlCP?ZT3?HlCP in the charged lepton sector, leading to the prediction of no CP violation, namely ? CP and the Majorana phases ? 21 and ? 31 are all equal to either zero or ?. We then propose an effective supersymmetric model based on the symmetry A4 ? H CP in which trimaximal lepton mixing is predicted together with either zero CP violation or ? CP ? ±?/2 with non-trivial Majorana phases. An ultraviolet completion of the effective model yields a neutrino mass matrix which depends on only three real parameters. As a result of this, all three CP phases and the absolute neutrino mass scale are determined, the atmospheric mixing angle is maximal, and the Dirac CP can either be preserved with ? CP ?=?0, ? or maximally broken with ? CP ?=?±?/2 and sharp predictions for the Majorana phases and neutrinoless double beta deca

    Branching fraction and CP asymmetry of the decays B+→K0Sπ+ and B+→K0SK+

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    An analysis of B+ → K0 Sπ+ and B+ → K0 S K+ decays is performed with the LHCb experiment. The pp collision data used correspond to integrated luminosities of 1 fb−1 and 2 fb−1 collected at centre-ofmass energies of √ s = 7 TeV and √ s = 8 TeV, respectively. The ratio of branching fractions and the direct CP asymmetries are measured to be B(B+ → K0 S K+ )/B(B+ → K0 Sπ+ ) = 0.064 ± 0.009 (stat.) ± 0.004 (syst.), ACP(B+ → K0 Sπ+ ) = −0.022 ± 0.025 (stat.) ± 0.010 (syst.) and ACP(B+ → K0 S K+ ) = −0.21 ± 0.14 (stat.) ± 0.01 (syst.). The data sample taken at √ s = 7 TeV is used to search for B+ c → K0 S K+ decays and results in the upper limit ( fc · B(B+ c → K0 S K+ ))/( fu · B(B+ → K0 Sπ+ )) < 5.8 × 10−2 at 90% confidence level, where fc and fu denote the hadronisation fractions of a ¯b quark into a B+ c or a B+ meson, respectively

    Measurement of the time-dependent CP asymmetry in B0 -> J/ψ KS0 decays

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    This Letter reports a measurement of the CP violation observables SJ/ψK0S and CJ/ψK0S in the decay channel B0→J/ψK0S performed with 1.0 fb−1 of pp collisions at s√=7 TeV collected by the LHCb experiment. The fit to the data yields SJ/ψK0S=0.73±0.07(stat)±0.04(syst) and CJ/ψK0S=0.03±0.09(stat)±0.01(syst). Both values are consistent with the current world averages and within expectations from the Standard Model

    Measurement of the CP-violating phase \phi s in Bs->J/\psi\pi+\pi- decays

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    Measurement of the mixing-induced CP-violating phase phi_s in Bs decays is of prime importance in probing new physics. Here 7421 +/- 105 signal events from the dominantly CP-odd final state J/\psi pi+ pi- are selected in 1/fb of pp collision data collected at sqrt{s} = 7 TeV with the LHCb detector. A time-dependent fit to the data yields a value of phi_s=-0.019^{+0.173+0.004}_{-0.174-0.003} rad, consistent with the Standard Model expectation. No evidence of direct CP violation is found

    A study of CP violation in B±→DK±B±→DK± and B±→Dπ±B±→Dπ± decays with D→KS0K±π∓ final states

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    A first study of CP violation in the decay modes B± → [K0S K ±π∓]Dh± and B± → [K0S K ∓π±]Dh±, where h labels a K or π meson and D labels a D0 or D0 meson, is performed. The analysis uses the LHCb data set collected in pp collisions, corresponding to an integrated luminosity of 3 fb−1. The analysis is sensitive to the CP-violating CKM phase γ through seven observables: one charge asymmetry in each of the four modes and three ratios of the charge-integrated yields. The results are consistent with measurements of γ using other decay modes

    Acquiring Maps of Interrelated Conjectures on Sharp Bounds

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    To automate the discovery of conjectures on combinatorial objects, we introduce the concept of a map of sharp bounds on characteristics of combinatorial objects, that provides a set of interrelated sharp bounds for these combinatorial objects. We then describe a Bound Seeker, a CP-based system, that gradually acquires maps of conjectures. The system was tested for searching conjectures on bounds on characteristics of digraphs: it constructs sixteen maps involving 431 conjectures on sharp lower and upper-bounds on eight digraph characteristics

    The response of intracellular signaling and muscle-protein metabolism to nutrition and exercise

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    In recent years, a body of literature examining the response of muscle-protein metabolism to exercise and nutrition has arisen. Developments in methods, especially stable isotopic tracer methodology, have allowed much information to be gathered in vivo in humans. The metabolic mechanism behind increased muscle mass requires that muscle-protein synthesis exceeds breakdown, i.e., net muscle-protein synthesis. Increased net muscle-protein balance may occur due to exercise, but net synthesis may occur only with the addition of nutrients, particularly a source of amino acids. The major impact of increased amino acid availability on net muscle-protein balance is due to stimulation of muscle-protein synthesis and less to inhibition of muscle-protein breakdown. Amino acids seem to stimulate muscle-protein synthesis, not only by mass action, i.e., providing substrate, but also as signals for initiation of protein synthesis. Stimulation of muscle-protein synthesis by amino acid ingestion may be linked to increased intracellular amino acid levels and/or to changing amino acid levels in the blood. Carbohydrate ingestion, most likely through the action of insulin, also may play a role in the response of muscle to exercise and nutrition. There is very little research in humans in vivo on the intracellular signaling that is linked to muscle-protein synthesis. It is clear that intracellular signaling responds to both insulin and amino acids, but the interactions with exercise are not well known; however, the details of the pathways have only just begun to be investigated, especially in humans. Delineation of these pathways is complicated, and there is little doubt that multiple intracellular signaling pathways with several levels of communication are involved in the hypertrophy process in response to nutrition and exercise. A systematic investigation of the relationship of the signaling to insulin and amino acids combined with exercise will provide important information, especially for populations vulnerable to muscle loss

    Measurement of the CP-violating phase phi(s) in (B)over-bar(s)(0) -> J / psi pi(+)pi(-) decays

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    The mixing-induced CP -violating phase ϕs in View the MathML source and View the MathML source decays is measured using the J/ψπ+π− final state in data, taken from 3 fb−1 of integrated luminosity, collected with the LHCb detector in 7 and 8 TeV centre-of-mass pp collisions at the LHC. A time-dependent flavour-tagged amplitude analysis, allowing for direct CP violation, yields a value for the phase ϕs=70±68±8 mrad. This result is consistent with the Standard Model expectation and previous measurements

    Stenus ornativentris SHARP 1886

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    Stenus ornativentris SHARP, 1886 Stenus ornativentris SHARP, 1885: 650; PUTHZ 2015: 1635. M a t e r i a l: VENEZUELA: 433: Los Chorros, V.1922, P. Psota (FMCh, cP). Neu für Venezuela.Published as part of Puthz, Volker, 2017, Übersicht über die neotropischen Arten der Gattung Stenus LATREILLE mit seitlich ungerandetem Abdomen und gelappten Tarsen (Coleoptera, Staphylinidae) 351. Beitrag zur Kenntnis der Steninen, pp. 749-883 in Linzer biologische Beiträge 49 (1) on page 828, DOI: 10.5281/zenodo.540980
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