132 research outputs found

    Magnetic and electronic structures of superconducting RuSr2_2GdCu2_2O8_8

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    The coexistence of ferromagnetism and superconductivity in RuSr2_2GdCu2_2O8_8 was reported both from experiments (by Tallon et. al.) and first-principles calculations (by Pickett et. al.). Here we report that our first-principles full-potential linearized augmented plane wave (FLAPW) calculations, employing the precise crystal structure with structural distortions (i.e., RuO6_6 rotations) determined by neutron diffraction, demonstrate that antiferromagnetic ordering of the Ru moments is energetically favored over the previously proposed ferromagnetic ordering. Our results are consistent with recently performed magnetic neutron diffraction experiments (Lynn et. al). Ru t2gt_{2g} states, which are responsible for the magnetism, have only a very small interaction with Cu ege_g states, which results in a small exchange splitting of these states. The Fermi surface, characterized by strongly hybridized dpσdp\sigma orbitals, has nesting features similar to those in the two-dimensional high TcT_c cuprate superconductors.Comment: 6 pages,6 figures, accepted for publication in Phys. Rev.

    Jet-quenching of the rotating heavy meson in a N{\mathcal{N}}=4 SYM plasma in presence of a constant electric field

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    In this paper, we consider a rotating heavy quark-antiquark (qqˉq\bar{q}) pair in a N{\mathcal{N}}=4 SYM thermal plasma. We assume that qqˉq\bar{q} center of mass moves at the speed vv and furthermore they rotate around the center of mass. We use the AdS/CFT correspondence and consider the effect of external electromagnetic field on the motion of the rotating meson. Then we calculate the jet-quenching parameter corresponding to the rotating meson in the constant electric field

    Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

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    Prostate cancer is a polygenic disease with a large heritable component. A number of common, low-penetrance prostate cancer risk loci have been identified through GWAS. Here we apply the Bayesian multivariate variable selection algorithm JAM to fine-map 84 prostate cancer susceptibility loci, using summary data from a large European ancestry meta-analysis. We observe evidence for multiple independent signals at 12 regions and 99 risk signals overall. Only 15 original GWAS tag SNPs remain among the catalogue of candidate variants identified; the remainder are replaced by more likely candidates. Biological annotation of our credible set of variants indicates significant enrichment within promoter and enhancer elements, and transcription factor-binding sites, including AR, ERG and FOXA1. In 40 regions at least one variant is colocalised with an eQTL in prostate cancer tissue. The refined set of candidate variants substantially increase the proportion of familial relative risk explained by these known susceptibility regions, which highlights the importance of fine-mapping studies and has implications for clinical risk profiling. © 2018 The Author(s).Prostate cancer is a polygenic disease with a large heritable component. A number of common, low-penetrance prostate cancer risk loci have been identified through GWAS. Here we apply the Bayesian multivariate variable selection algorithm JAM to fine-map 84 prostate cancer susceptibility loci, using summary data from a large European ancestry meta-analysis. We observe evidence for multiple independent signals at 12 regions and 99 risk signals overall. Only 15 original GWAS tag SNPs remain among the catalogue of candidate variants identified; the remainder are replaced by more likely candidates. Biological annotation of our credible set of variants indicates significant enrichment within promoter and enhancer elements, and transcription factor-binding sites, including AR, ERG and FOXA1. In 40 regions at least one variant is colocalised with an eQTL in prostate cancer tissue. The refined set of candidate variants substantially increase the proportion of familial relative risk explained by these known susceptibility regions, which highlights the importance of fine-mapping studies and has implications for clinical risk profiling. © 2018 The Author(s).Peer reviewe

    Measurement of the WW production cross section in p anti-p collisions at s**(1/2) = 1.96 TeV

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    We present a measurement of the W boson pair-production cross section in p anti-p collisions at a center-of-mass energy of sqrt{s}=1.96 TeV. The data, collected with the Run II DO detector, correspond to an integrated luminosity of 224-252 pb^-1 depending on the final state (ee, emu or mumu). We observe 25 candidates with a background expectation of 8.1+/-0.6(stat)+/-0.6(syst)+/-0.5(lum) events. The probability for an upward fluctuation of the background to produce the observed signal is 2.3x10^-7, equivalent to 5.2 standard deviations.The measurement yields a cross section of 13.8+4.3/-3.8(stat)+1.2/-0.9(syst)+/-0.9(lum) pb, in agreement with predictions from the standard model.Comment: submitted to PR

    Measurement of the Lambda^0_b lifetime in the decay Lambda^0_b -> J/psi Lambda^0 with the D0 Detector

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    We present measurements of the Lambda^0_b lifetime in the exclusive decay channel Lambda^0_{b}->J/psi Lambda^0, with J/psi to mu+ mu- and Lambda^0 to p pi-, the B^0 lifetime in the decay B^0 -> J/psi K^0_S with J/psi to mu+ mu- and K^0_S to pi+ pi-, and the ratio of these lifetimes. The analysis is based on approximately 250 pb^{-1} of data recorded with the D0 detector in pp(bar) collisions at sqrt{s}=1.96 TeV. The Lambda^0_b lifetime is determined to be tau(Lambda^0_b) = 1.22 +0.22/-0.18 (stat) +/- 0.04 (syst) ps, the B^0 lifetime tau(B^0) = 1.40 +0.11/-0.10 (stat) +/- 0.03 (syst) ps, and the ratio tau(Lambda^0_b)/tau(B^0) = 0.87 +0.17/-0.14 (stat) +/- 0.03 (syst). In contrast with previous measurements using semileptonic decays, this is the first determination of the Lambda^0_b lifetime based on a fully reconstructed decay channel.Comment: 7 pages, 4 figures, Submitted to Physical Review Letters, v2: Added FNAL Pub-numbe

    Erratum to Measurement of σ(ppˉZ)Br(Zττ)\sigma (p \bar p \to Z) \cdot Br(Z \to \tau\tau) at s=\bm{\sqrt{s}=}1.96 TeV, published in Phys. Rev. D {71}, 072004 (2005)

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    A change in estimated integrated luminosity (from 226 pb1to257pb^{-1} to 257 pb^{-1}leadstoacorrectedvaluefor leads to a corrected value for {\sigma (p \bar p \to Z) \cdot}BrBr{(Z \to \tau \tau)}of of 209\pm13(stat.)\pm16(syst.)\pm13(lum) pb

    First sagittarius A* Event Horizon Telescope results. VI. Testing the black hole metric

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    Galaxie

    Resolving the inner parsec of the blazar J1924-2914 with the event horizon telescope

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    Galaxie
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