1,067 research outputs found

    NASA RECON: Course Development, Administration, and Evaluation

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    The R and D activities addressing the development, administration, and evaluation of a set of transportable, college-level courses to educate science and engineering students in the effective use of automated scientific and technical information storage and retrieval systems, and, in particular, in the use of the NASA RECON system, are discussed. The long-range scope and objectives of these contracted activities are overviewed and the progress which has been made toward these objectives during FY 1983-1984 is highlighted. In addition, the results of a survey of 237 colleges and universities addressing course needs are presented

    The impact of azithromycin therapy on the airway microbiota in asthma

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    There is interest in the use of macrolide antibiotics in asthma. Macrolides have been shown to improve airway hyperresponsiveness (AHR) and measures of airway inflammation.The degree of AHR may relate to the microbiota present in the airways, with a recent study reporting that patients with asthma with a significant improvement in AHR following treatment with clarithromycin had a higher bacterial diversity prior to treatment. To our knowledge, the impact on the asthmatic airway microbiota of an antibiotic has not been reported and we therefore set out to establish if macrolide therapy was associated with a change in airway microbiota in asthma

    On the Particle Data Group evaluation of Psi' and chi_c Branching Ratios

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    I propose a new evaluation of ψ(2S)\psi'(2S) and χc(1P)\chi_c(1P) branching ratios which avoids the correlations affecting the current Particle Data Group evaluation. These correlations explain the apparent technique-dependent discrepancies between the available determinations of the B(χc(1P)ppˉ){\cal B}(\chi_c(1P)\to p\bar p) and Γ(χc(1P)γγ)\Gamma(\chi_c(1P)\to \gamma\gamma) under the hypotesis that the current values of the ψ(2S)χc(1P)γ\psi'(2S)\to\chi_c(1P)\gamma branching ratios are overestimated. In the process I also noticed that Particle Data Group has not restated many of the older measurements, when necessary, for the new value of B(J/ψl+l){\cal B}(J/\psi\to l^+l^-), which significantly affects the evaluation of some relevant ψ(2S)\psi'(2S) and χc(1P)\chi_c(1P) exclusive branching ratios.Comment: 13 pages. Revised version. Submitted to Phys. Rev.

    The Baculovirus Uses a Captured Host Phosphatase to Induce Enhanced Locomotory Activity in Host Caterpillars

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    The baculovirus is a classic example of a parasite that alters the behavior or physiology of its host so that progeny transmission is maximized. Baculoviruses do this by inducing enhanced locomotory activity (ELA) that causes the host caterpillars to climb to the upper foliage of plants. We previously reported that this behavior is not induced in silkworms that are infected with a mutant baculovirus lacking its protein tyrosine phosphatase (ptp) gene, a gene likely captured from an ancestral host. Here we show that the product of the ptp gene, PTP, associates with baculovirus ORF1629 as a virion structural protein, but surprisingly phosphatase activity associated with PTP was not required for the induction of ELA. Interestingly, the ptp knockout baculovirus showed significantly reduced infectivity of larval brain tissues. Collectively, we show that the modern baculovirus uses the host-derived phosphatase to establish adequate infection for ELA as a virion-associated structural protein rather than as an enzyme

    Measurements of the Ratios B(Ds+η+ν)/B(Ds+ϕ+ν){\cal B}(D_s^+\to \eta\ell^+\nu)/{\cal B}(D_s^+\to \phi\ell^+\nu) and B(Ds+η+ν)/B(Ds+ϕ+ν){\cal B}(D_s^+\to \eta'\ell^+\nu)/{\cal B}(D_s^+\to \phi\ell^+\nu)

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    Using the CLEO~II detector we measure B(Ds+ηe+ν)/B(Ds+ϕe+ν)=1.24±0.12±0.15{\cal B}(D_s^+\to \eta e^+\nu)/{\cal B}(D_s^+\to \phi e^+\nu) =1.24\pm0.12\pm0.15, B(Ds+ηe+ν)/B(Ds+ϕe+ν)=0.43±0.11±0.07{\cal B}(D_s^+\to \eta' e^+\nu)/{\cal B}(D_s^+\to \phi e^+\nu) =0.43\pm0.11\pm0.07 and B(Ds+ηe+ν)/B(Ds+ηe+ν)=0.35±0.09±0.07{\cal B}(D_s^+\to \eta' e^+\nu)/{\cal B}(D_s^+\to \eta e^+\nu) =0.35\pm0.09\pm0.07. We find the vector to pseudoscalar ratio, B(Ds+ϕe+ν)/B(Ds+(η+η)e+ν)=0.60±0.06±0.06{\cal B}(D_s^+\to \phi e^+\nu)/{\cal B}(D_s^+\to (\eta+\eta') e^+\nu) =0.60\pm0.06\pm0.06, which is similar to the ratio found in non strange DD decays.Comment: 11 page uuencoded postscript file, postscript file also available through http://w4.lns.cornell.edu/public/CLN

    Measurement of the Inclusive Semi-electronic D0D^0 Branching Fraction

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    Using the angular correlation between the π+\pi^+ emitted in a D+D0π+D^{*+} \rightarrow D^0 \pi^+ decay and the e+e^+ emitted in the subsequent D0Xe+νD^0 \rightarrow Xe^+\nu decay, we have measured the branching fraction for the inclusive semi-electronic decay of the D0D^0 meson to be: {\cal B}(D^0 \rightarrow X e^+ \nu) = [6.64 \pm 0.18 (stat.) \pm 0.29 (syst.)] \%. The result is based on 1.7 fb1^{-1} of e+ee^+e^- collisions recorded by the CLEO II detector located at the Cornell Electron Storage Ring (CESR). Combining the analysis presented in this paper with previous CLEO results we find, \frac{{\cal B} (D^0 \rightarrow X e^+ \nu)} {{\cal B} (D^0 \rightarrow K^- \pi^+)} = 1.684 \pm 0.056 (stat.) \pm 0.093(syst.) and \frac{{\cal B}(D\rightarrow K^-e^+\nu)} {{\cal B}(D\rightarrow Xe^+\nu)} = 0.581 \pm 0.023 (stat.) \pm 0.028(syst.). The difference between the inclusive rate and the sum of the measured exclusive branching fractions (measured at CLEO and other experiments) is (3.3±7.2)%(3.3 \pm 7.2) \% of the inclusive rate.Comment: Latex file, 33pages, 4 figures Submitted to PR

    Search for Exclusive Charmless Hadronic B Decays

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    We have searched for two-body charmless hadronic decays of BB mesons. Final states include ππ\pi\pi, KπK \pi, and KKKK with both charged and neutral kaons and pions; πρ\pi\rho, KρK \rho, and KπK^*\pi; and KϕK\phi, Kϕ K^*\phi, and ϕϕ\phi\phi. The data used in this analysis consist of 2.6~million BBˉB\bar{B}~pairs produced at the Υ(4S)\Upsilon(4S) taken with the CLEO-II detector at the Cornell Electron Storage Ring (CESR). We measure the branching fraction of the sum of B0π+πB^0 \rightarrow \pi^+\pi^- and B0K+πB^0 \rightarrow K^+\pi^- to be (1.80.50.3+0.6+0.2±0.2)×105(1.8^{+0.6+0.2}_{-0.5-0.3}\pm0.2) \times 10^{-5}. In addition, we place upper limits on individual branching fractions in the range from 10410^{-4} to 10610^{-6}.Comment: 33 page LATEX file, uses REVTEX and psfig, 14 figures in a separate uuencoded postscript file, postscript version also available through http://w4.lns.cornell.edu/public/CLN

    Semileptonic Branching Fraction of Charged and Neutral B Mesons

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    An examination of leptons in Υ(4S){\Upsilon (4S)} events tagged by reconstructed BB decays yields semileptonic branching fractions of b=(10.1±1.8±1.4)%b_-=(10.1 \pm 1.8\pm 1.4)\% for charged and b0=(10.9±0.7±1.1)%b_0=(10.9 \pm 0.7\pm 1.1)\% for neutral BB mesons. This is the first measurement for charged BB. Assuming equality of the charged and neutral semileptonic widths, the ratio b/b0=0.93±0.18±0.12b_-/b_0=0.93 \pm 0.18 \pm 0.12 is equivalent to the ratio of lifetimes. A postscript version is available through World-Wide-Web in http://w4.lns.cornell.edu/public/CLNS/1994Comment: 9 pages (in REVTEX format) Preprint CLNS94-1286, CLEO 94-1

    Observation of the Isospin-Violating Decay Ds+Ds+π0D_s^{*+}\to D_s^+\pi^0

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    Using data collected with the CLEO~II detector, we have observed the isospin-violating decay Ds+Ds+π0D_s^{*+}\to D_s^+\pi^0. The decay rate for this mode, relative to the dominant radiative decay, is found to be Γ(Ds+Ds+π0)/Γ(Ds+Ds+γ)=0.0620.018+0.020±0.022\Gamma(D_s^{*+}\to D_s^+\pi^0)/\Gamma(D_s^{*+}\to D_s^+\gamma)= 0.062^{+0.020}_{-0.018}\pm0.022.Comment: 8 page uuencoded postscript file, also available through http://w4.lns.cornell.edu/public/CLN
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