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Träfflista för sökning "WFRF:(Agnew L.) "

Sökning: WFRF:(Agnew L.)

  • Resultat 61-67 av 67
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61.
  • Abazov, V. M., et al. (författare)
  • Measurement of direct CP violation parameters in B-+/- -> J/psi K-+/- and B-+/- -> J/psi pi(+/-) decays with 10.4 fb(-1) of Tevatron data
  • 2013
  • Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 110:24, s. 241801-
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a measurement of the direct CP-violating charge asymmetry in B-+/- mesons decaying to J/psi K-+/- and J/psi pi(+/-) where J/psi decays to mu(+)mu(-), using the full run II data set of 10.4 fb(-1) of proton-antiproton collisions collected using the D0 detector at the Fermilab Tevatron Collider. A difference in the yield of B- and B+ mesons in these decays is found by fitting to the difference between their reconstructed invariant mass distributions resulting in asymmetries of A(J/psi K) = [0.59 +/- 0.37]%, which is the most precise measurement to date, and A(J/psi pi) = [-4.2 +/- 4.5]%. Both measurements are consistent with standard model predictions.
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62.
  • Abazov, V. M., et al. (författare)
  • Measurement of the W boson mass with the D0 detector
  • 2014
  • Ingår i: Physical Review D. - 1550-7998 .- 1550-2368. ; 89:1, s. 012005-
  • Tidskriftsartikel (refereegranskat)abstract
    • We give a detailed description of the measurement of the W boson mass, M-W, performed on an integrated luminosity of 4.3 fb(-1), which is based on similar techniques as used for our previous measurement done on an independent data set of 1 fb(-1) of data. The data were collected using the D0 detector at the Fermilab Tevatron Collider. This data set yields 1.68 x 10(6) W -> ev candidate events. We measure the mass using the transverse mass, electron transverse momentum, and missing transverse energy distributions. The M-W measurements using the transverse mass and the electron transverse momentum distributions are the most precise of these three and are combined to give M-W 80.367 +/- 0.013 (stat) +/- 0.022(syst) GeV = 80: 367 +/- 0.026 GeV. When combined with our earlier measurement on 1 fb(-1) of data, we obtain M-W = 80.375 +/- 0.023 GeV.
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63.
  • Abazov, V. M., et al. (författare)
  • Measurement of the ZZ production cross section and search for the standard model Higgs boson in the four lepton final state in p(p)over-bar collisions
  • 2013
  • Ingår i: Physical Review D. - 1550-7998 .- 1550-2368. ; 88:3, s. 032008-
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a measurement of Z boson pair production in p (p) over bar collisions at 1.96 TeV with 9.6 to 9.8 fb(-1) of D0 data. We examine the final states eeee, ee mu mu, and mu mu mu mu. Based on selected data, the measured cross section in the mass region M(Z/gamma*) > 30 GeV is sigma(p (p) over bar -> Z/gamma*Z/gamma*) = 1.26(-0.36)(+0.44)(stat)(-0.15)(+0.17) X (syst) +/- 0.08 (lumi) pb; after correcting for the expected ratio of sigma (p (p) over bar -> Z/gamma*Z/gamma*) to sigma(p (p) over bar -> ZZ), we derive a cross section for p (p) over bar -> ZZ production of 1.05(-0.30)(+0.37)(stat)(-0.12)(0.14)(syst) +/- 0.06 (lumi) pb. This result is combined with a previous result from the ZZ -> l(+)l(-) nu(nu) over bar channel resulting in a combined p (p) over bar -> ZZ cross section measurement of 1.32(-0.25)(+0.29) (stat) +/- 0.12 (syst) +/- 0.04 (lumi) pb. These measurements are consistent with the standard model expectation of 1.43 +/- 0.10 pb. We extend this analysis to search for the standard model (SM) Higgs boson between 115 and 200 GeV. At a Higgs boson mass of 125 GeV, we expect to set a limit of 43 times the SM expectation at 95% C.L., and set a limit of 42 times the SM expectation at 95% C.L.
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64.
  • Abazov, V. M., et al. (författare)
  • Search for anomalous quartic WW gamma gamma couplings in dielectron and missing energy final states in p(p)over-bar collisions at root s 1.96 TeV
  • 2013
  • Ingår i: Physical Review D. - 1550-7998 .- 1550-2368. ; 88:1, s. 012005-
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a search for anomalous components of the quartic gauge boson coupling WW gamma gamma in events with an electron, a positron and missing transverse energy. The analyzed data correspond to 9.7 fb(-1) of integrated luminosity collected by the D0 detector in p (p) over bar collisions at root s 1.96 TeV. The presence of anomalous quartic gauge couplings would manifest itself as an excess of boosted WW events. No such excess is found in the data, and we set the most stringent limits to date on the anomalous coupling parameters a(0)(W) and a(C)(W). When a form factor with Lambda(cutoff) = 0.5 TeV is used, the observed upper limits at 95% C. L. are vertical bar a(0)(W)/Lambda(2)vertical bar < 0.0025 GeV-2 and vertical bar a(C)(W)/Lambda(2)vertical bar < 0.0092 GeV-2.
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65.
  • Keogan, Katharine, et al. (författare)
  • Global phenological insensitivity to shifting ocean temperatures among seabirds
  • 2018
  • Ingår i: Nature Climate Change. - : Springer Science and Business Media LLC. - 1758-678X .- 1758-6798. ; 8:4, s. 313-318
  • Tidskriftsartikel (refereegranskat)abstract
    • Reproductive timing in many taxa plays a key role in determining breeding productivity(1), and is often sensitive to climatic conditions(2). Current climate change may alter the timing of breeding at different rates across trophic levels, potentially resulting in temporal mismatch between the resource requirements of predators and their prey(3). This is of particular concern for higher-trophic-level organisms, whose longer generation times confer a lower rate of evolutionary rescue than primary producers or consumers(4). However, the disconnection between studies of ecological change in marine systems makes it difficult to detect general changes in the timing of reproduction(5). Here, we use a comprehensive meta-analysis of 209 phenological time series from 145 breeding populations to show that, on average, seabird populations worldwide have not adjusted their breeding seasons over time (-0.020 days yr(-1)) or in response to sea surface temperature (SST) (-0.272 days degrees C-1) between 1952 and 2015. However, marked between-year variation in timing observed in resident species and some Pelecaniformes and Suliformes (cormorants, gannets and boobies) may imply that timing, in some cases, is affected by unmeasured environmental conditions. This limited temperature-mediated plasticity of reproductive timing in seabirds potentially makes these top predators highly vulnerable to future mismatch with lower-trophic-level resources(2).
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66.
  • Mitchell, T., et al. (författare)
  • Evidence of cardiac involvement in the fetal inflammatory response syndrome: disruption of gene networks programming cardiac development in nonhuman primates
  • 2018
  • Ingår i: American Journal of Obstetrics and Gynecology. - : Elsevier BV. - 0002-9378. ; 218:4
  • Tidskriftsartikel (refereegranskat)abstract
    • BACKGROUND: Most early preterm births are associated with intraamniotic infection and inflammation, which can lead to systemic inflammation in the fetus. The fetal inflammatory response syndrome describes elevations in the fetal interleukin-6 level, which is a marker for inflammation and fetal organ injury. An understanding of the effects of inflammation on fetal cardiac development may lead to insight into the fetal origins of adult cardiovascular disease. OBJECTIVE: The purpose of this study was to determine whether the fetal inflammatory response syndrome is associated with disruptions in gene networks that program fetal cardiac development. STUDY DESIGN: We obtained fetal cardiac tissue after necropsy from a well-described pregnant nonhuman primate model (pigtail macaque, Macaca nemestrina) of intrauterine infection (n = 5) and controls (n = 5). Cases with the fetal inflammatory response syndrome (fetal plasma interleukin-6 >11 pg/mL) were induced by either choriodecidual inoculation of a hypervirulent group B streptococcus strain (n = 4) or intraamniotic inoculation of Escherichia coli (n = 1). RNA and protein were extracted from fetal hearts and profiled by microarray and Luminex (Millipore, Billerica, MA) for cytokine analysis, respectively. Results were validated by quantitative reverse transcriptase polymerase chain reaction. Statistical and bioinformatics analyses included single gene analysis, gene set analysis, Ingenuity Pathway Analysis (Qiagen, Valencia, CA), and Wilcoxon rank sum. RESULTS: Severe fetal inflammation developed in the context of intraamniotic infection and a disseminated bacterial infection in the fetus. Interleukin-6 and -8 in fetal cardiac tissues were elevated significantly in fetal inflammatory response syndrome cases vs controls (P<.05). A total of 609 probe sets were expressed differentially (>1.5-fold change, P<.05) in the fetal heart (analysis of variance). Altered expression of select genes was validated by quantitative reverse transcriptase polymerase chain reaction that included several with known functions in cardiac injury, morphogenesis, angiogenesis, and tissue remodeling (eg, angiotensin I converting enzyme 2, STEAP family member 4, natriuretic peptide A, and secreted frizzled-related protein 4; all P<.05). Multiple gene sets and pathways that are involved in cardiac morphogenesis and vasculogenesis were downregulated significantly by gene set and Ingenuity Pathway Analysis (hallmark transforming growth factor beta signaling, cellular morphogenesis during differentiation, morphology of cardiovascular system; all P<.05). CONCLUSION: Disruption of gene networks for cardiac morphogenesis and vasculogenesis occurred in the preterm fetal heart of nonhuman primates with preterm labor, intraamniotic infection, and severe fetal inflammation. Inflammatory injury to the fetal heart in utero may contribute to the development of heart disease later in life. Development of preterm labor therapeutics must also target fetal inflammation to lessen organ injury and potential long-term effects on cardiac function.
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67.
  • Rapson, G.L., et al. (författare)
  • Subalpine gully-head ribbon fens of the Lammerlaw and Lammermoor Ranges, Otago, New Zealand
  • 2006
  • Ingår i: New Zealand Journal of Botany. - 0028-825X. ; 44, s. 351-375
  • Tidskriftsartikel (refereegranskat)abstract
    • Vegetation patterns of subalpine gully-head mires were investigated in the flat-topped Lammerlaw and Lammermoor Ranges, South Island, New Zealand. Two intensively studied mires each consist of a series of peaty terraces and scarps. Terraces may contain pools, elongated downslope in the narrow, lower altitude mire, but across slope in the broader, upper mire. A crest occurs on some terrace lips, and marginal "spillways" (channel-like zones) occur down some scarps. Some mires have drained by subsurface pipes. Vegetation analysis distinguished between grassland or herbfield on gully sides, vegetation of mire margins, showing aspect differences on the steeper, lower mire, and the vegetation of gully floors, including oligotrophic mire centre vegetation and species-poor pools. The crests, though warmer, bore no special vegetation type. Mineral soil beneath the peat indicates a previous non-mire vegetation, which has subsequently paludified. Scarp slumps indicate downslope creep of organic material. Peat fissures, and mineral, vegetation, and erosion dams all appear to have initiated development of some pools. Mires are designated gully-head ribbon fens. Patterning appears to be accentuated because of the mires' gully-head location on broad-topped ranges, and drainage of soligenous water from upslope gully sides. These apparently unique fens give insight into patterning in aapa mires, and merit special conservation.
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