101 research outputs found

    Classification of Inflationary Einstein--Scalar--Field--Models via Catastrophe Theory

    Full text link
    Various scenarios of the initial inflation of the universe are distinguished by the choice of a scalar field {\em potential} U(ϕ)U(\phi) which simulates a {\it temporarily} non--vanishing {\em cosmological term}. Our new method, which involves a reparametrization in terms of the Hubble expansion parameter HH, provides a classification of allowed inflationary potentials and of the stability of the critical points. It is broad enough to embody all known {\it exact} solutions involving one scalar field as special cases. Inflation corresponds to the evolution of critical points of some catastrophe manifold. The coalescence of its nondegenerate critical points with the creation of a degenerate critical point corresponds the reheating phase of the universe. This is illustrated by several examples.Comment: 12 pages, REVTeX, no figure

    Study of Lambda/c+ Cabibbo Favored Decays Containing a Lambda Baryon in the Final State

    Full text link
    Using data from the FOCUS experiment (FNAL-E831), we study the decay of Λc+\Lambda^+_c baryons into final states containing a Λ\Lambda hyperon. The branching fractions of Λc+\Lambda^+_c into Λπ+\Lambda \pi^+, Λπ+π+π\Lambda \pi^+ \pi^+ \pi^- and ΛKˉ0K+\Lambda \bar{K} ^0 K^+ relative to that into pKπ+pK^-\pi^+ are measured to be 0.217±0.013±0.0200.217 \pm 0.013 \pm 0.020, 0.508±0.024±0.0240.508 \pm 0.024 \pm 0.024 and 0.142±0.018±0.0220.142 \pm 0.018 \pm 0.022, respectively. We also report new measurements of Γ(Λc+Σ0π+)Γ(Λc+Λπ+)=1.09±0.11±0.19\frac{\Gamma(\Lambda^+_c \to \Sigma^0 \pi^+)}{\Gamma(\Lambda^+_c \to \Lambda \pi^+)} = 1.09 \pm 0.11 \pm 0.19, Γ(Λc+Σ0π+π+π)Γ(Λc+Λπ+π+π)=0.26±0.06±0.09\frac{\Gamma(\Lambda^+_c \to \Sigma^0 \pi^+\pi^+ \pi^-)}{\Gamma(\Lambda^+_c \to \Lambda \pi^+ \pi^+ \pi^-)} = 0.26 \pm 0.06 \pm 0.09 and Γ(Λc+Ξ(1690)0(ΛKˉ0)K+)Γ(Λc+ΛKˉ0K+)=0.33±0.10±0.04\frac{\Gamma(\Lambda^+_c \to \Xi(1690)^0(\Lambda \bar{K} ^0) K^+)}{\Gamma(\Lambda^+_c \to \Lambda \bar{K} ^0 K^+)} = 0.33 \pm 0.10 \pm 0.04. Further, an analysis of the subresonant structure for the Λc+Λπ+π+π\Lambda^+_c \to \Lambda \pi^+\pi^+\pi^- decay mode is presented.Comment: 14 pages, 6 figures, 3 tables, Submitted to Physics Letter

    Mass Splitting and Production of Σc0\Sigma_c^0 and Σc++\Sigma_c^{++} Measured in 500GeV500 {GeV} π\pi^- -N Interactions

    Full text link
    From a sample of 2722±782722 \pm 78 Λc+\Lambda_c^+ decaying to the pKπ+pK^-\pi^+ final state, we have observed, in the hadroproduction experiment E791 at Fermilab, 143±20143 \pm 20 Σc0\Sigma_c^0 and 122±18122 \pm 18 Σc++\Sigma_c^{++} through their decays to Λc+π±\Lambda_c^+ \pi^{\pm}. The mass difference M(Σc0)M(Λc+M(\Sigma_c^0) - M(\Lambda_c^+) is measured to be (167.38±0.29±0.15)MeV(167.38\pm 0.29\pm 0.15) {MeV}; for M(Σc++)M(Λc+)M(\Sigma_c^{++}) - M(\Lambda_c^+), we find (167.76±0.29±0.15)MeV(167.76\pm 0.29\pm0.15) {MeV}. The rate of Λc+\Lambda_c^+ production from decays of the Σc\Sigma_c triplet is (22\pm 2\pm 3) {%} of the total Λc+\Lambda_c^+ production assuming equal rate of production from all three, as measured for Σc0\Sigma_c^0 and Σc++\Sigma_c^{++}. We do not observe a statistically significant Σc\Sigma_c baryon-antibaryon production asymmetry. The xFx_F and pt2p_t^2 spectra of Λc+\Lambda_c^+ from Σc\Sigma_c decays are observed to be similar to those for all Λc+\Lambda_c^+'s produced.Comment: 15 pages, uuencoded postscript 3 figures uuencoded, tar-compressed fil

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

    Full text link
    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

    Measurements of the Sigma_c^0 and Sigma_c^{++} Mass Splittings

    Full text link
    Using a high statistics sample of photoproduced charmed particles from the FOCUS experiment at Fermilab (FNAL-E831), we measure the mass splittings of the charmed baryons Sigma_c^0 and Sigma_c^{++}. We find M(Sigma_c^0 - Lambda_c^+) = 167.38 +/- 0.21 +/- 0.13 MeV/c^2 and M(Sigma_c^++ - Lambda_c^+) = 167.35 +/- 0.19 +/- 0.12 MeV/c^2 with samples of 362 +/- 36 and 461 +/- 39 events, respectively. We measure the isospin mass splitting M(Sigma_c^++ - Sigma_c^0) to be -0.03 +/- 0.28 +/- 0.11 Mev/c^2. The first errors are statistical and the second are systematic.Comment: 10 pages, 2 figure

    Study of Hadronic Five-Body Decays of Charmed Mesons Involving KS0K_S^0

    Get PDF
    We study the decay of D0D^0 and Ds+D^+_s mesons into five-body final states including a KS0K_S^0 and report the discovery of the decay mode Ds+KS0KS0π+π+πD_s^+\to K_S^0 K_S^0\pi^+\pi^+\pi^-. The branching ratio for the new mode is {Γ(Ds+KS0KS0π+ππ+)Γ(Ds+KS0Kπ+π+){\Gamma(D_s^+\to K_S^0K_S^0\pi^+\pi^-\pi^+)} \over {\Gamma(D_s^+\to K_S^0K^-\pi^+\pi^+)}} = 0.102±0.029±\pm0.029\pm0.029. We also determine the branching ratio of {Γ(D0KS0π+π+ππ)Γ(D0KS0π+π){\Gamma(D^0\to K_S^0\pi^+\pi^+\pi^-\pi^-)} \over {\Gamma(D^0 \to K_S^0\pi^+\pi^-)}} = 0.095±0.005±\pm0.005\pm0.007 as well as an upper limit for {Γ(D0KS0Kπ+π+π)Γ(D0KS0π+π+ππ){\Gamma(D^0\to K_S^0K^-\pi^+\pi^+\pi^-)} \over {\Gamma(D^0\to K_S^0\pi^+\pi^+\pi^-\pi^-)}} << 0.054 (90% CL). An analysis of the resonant substructure for D0KS0π+π+ππD^0 \to K_S^0\pi^+\pi^+\pi^-\pi^- is also performed

    Experimental evidence for a light and broad scalar resonance in D+ππ+π+D^+\to \pi^-\pi^+\pi^+ decay

    Full text link
    From a sample of 1172±611172 \pm 61 D+ππ+π+D^+ \to \pi^- \pi^+ \pi^+ decay, we find Γ(D+ππ+π+)/Γ(D+Kπ+π+)=0.0311±0.00180.0026+0.0016\Gamma (D^+ \to \pi^- \pi^+ \pi^+) / \Gamma (D^+ \to K^- \pi^+ \pi^+) = 0.0311 \pm 0.0018 ^{+0.0016}_{-0.0026}. Using a coherent amplitude analysis to fit the Dalitz plot of this decays, we find strong evidence that a scalar resonance of mass 47823+24±17478^{+24}_{-23} \pm 17 MeV/c2c^2 and width 32440+42±21324^{+42}_{-40} \pm 21 MeV/c2c^2 accounts for approximately half of all decays.Comment: 10 pages, 3 eps figure

    Dalitz Plot Analysis of the Decay D^+ --> K^- pi^+ pi^+ and Indication of a Low-Mass Scalar K pi Resonance

    Full text link
    We study the Dalitz plot of the decay D^+ --> K^- pi^+ pi^+ with a sample of 15090 events from Fermilab experiment E791. Modeling the decay amplitude as the coherent sum of known K pi resonances and a uniform nonresonant term, we do not obtain an acceptable fit. If we allow the mass and width of the K^*_0(1430) to float, we obtain values consistent with those from PDG but the chi^2 per degree of freedom of the fit is still unsatisfactory. A good fit is found when we allow for the presence of an additional scalar resonance, with mass 797 +/- 19 +/- 43 MeV/c^2 and width 410 +/- 43 +/- 87 MeV/c^2. The mass and width of the K^*_0(1430) become 1459 +/- 7 +/- 5 MeV/c^2 and 175 +/- 12 +/- 12 MeV/c^2, respectively. Our results provide new information on the scalar sector in hadron spectroscopy.Comment: Accepted for publication in Physical Review Letter

    A measurement of branching ratios of D+D^+ and Ds+D^+_s hadronic decays to four-body final states containing a KSK_S

    Full text link
    We have studied hadronic four-body decays of D+D^+ and Ds+D^+_s mesons with a KSK_S in the final state using data recorded during the 1996-1997 fixed-target run at Fermilab high energy photoproduction experiment FOCUS. We report a new branching ratio measurement of Γ(D+KSKπ+π+)/Γ(D+KSπ+π+π)=0.0768±0.0041±0.0032\Gamma(D^+\to K_S K^-\pi^+\pi^+)/\Gamma(D^+\to K_S \pi^+\pi^+\pi^-)=0.0768\pm0.0041\pm0.0032. We make the first observation of three new decay modes with branching ratios Γ(D+KSK+π+π)/Γ(D+KSπ+π+π)=0.0562±0.0039±0.0040\Gamma(D^+\to K_S K^+\pi^+\pi^-)/\Gamma(D^+\to K_S \pi^+\pi^+\pi^-)=0.0562\pm0.0039\pm0.0040, \Gamma(D^+\to\K_S K^+ K^-\pi^+)/\Gamma(D^+\to K_S \pi^+\pi^+\pi^-)=0.0077\pm0.0015\pm0.0009, and Γ(Ds+KSK+π+π)/Γ(Ds+KSKπ+π+)=0.586±0.052±0.043\Gamma(D^+_s\to K_S K^+\pi^+\pi^-)/\Gamma(D^+_s\to K_S K^-\pi^+\pi^+)=0.586\pm0.052\pm0.043, where in each case the first error is statistical and the second error is systematic.Comment: 4 pages, 1 table, 2 figures, submitted to Physical Review Letter

    Human Immunodeficiency Virus Impairs Reverse Cholesterol Transport from Macrophages

    Get PDF
    Several steps of HIV-1 replication critically depend on cholesterol. HIV infection is associated with profound changes in lipid and lipoprotein metabolism and an increased risk of coronary artery disease. Whereas numerous studies have investigated the role of anti-HIV drugs in lipodystrophy and dyslipidemia, the effects of HIV infection on cellular cholesterol metabolism remain uncharacterized. Here, we demonstrate that HIV-1 impairs ATP-binding cassette transporter A1 (ABCA1)-dependent cholesterol efflux from human macrophages, a condition previously shown to be highly atherogenic. In HIV-1–infected cells, this effect was mediated by Nef. Transfection of murine macrophages with Nef impaired cholesterol efflux from these cells. At least two mechanisms were found to be responsible for this phenomenon: first, HIV infection and transfection with Nef induced post-transcriptional down-regulation of ABCA1; and second, Nef caused redistribution of ABCA1 to the plasma membrane and inhibited internalization of apolipoprotein A-I. Binding of Nef to ABCA1 was required for down-regulation and redistribution of ABCA1. HIV-infected and Nef-transfected macrophages accumulated substantial amounts of lipids, thus resembling foam cells. The contribution of HIV-infected macrophages to the pathogenesis of atherosclerosis was supported by the presence of HIV-positive foam cells in atherosclerotic plaques of HIV-infected patients. Stimulation of cholesterol efflux from macrophages significantly reduced infectivity of the virions produced by these cells, and this effect correlated with a decreased amount of virion-associated cholesterol, suggesting that impairment of cholesterol efflux is essential to ensure proper cholesterol content in nascent HIV particles. These results reveal a previously unrecognized dysregulation of intracellular lipid metabolism in HIV-infected macrophages and identify Nef and ABCA1 as the key players responsible for this effect. Our findings have implications for pathogenesis of both HIV disease and atherosclerosis, because they reveal the role of cholesterol efflux impairment in HIV infectivity and suggest a possible mechanism by which HIV infection of macrophages may contribute to increased risk of atherosclerosis in HIV-infected patients
    corecore