768 research outputs found

    Measurement of the production of charm jets tagged with D0^{0} mesons in pp collisions at s\sqrt{s}= 7 TeV

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    The production of charm jets in proton-proton collisions at a center-of-mass energy of s=7\sqrt{s}=7 TeV was measured with the ALICE detector at the CERN Large Hadron Collider. The measurement is based on a data sample corresponding to a total integrated luminosity of 6.236.23 nb1{\rm nb}^{-1}, collected using a minimum-bias trigger. Charm jets are identified by the presence of a D0^0 meson among their constituents. The D0^0 mesons are reconstructed from their hadronic decay D0^0\rightarrowKπ+^{-}\pi^{+}. The D0^0-meson tagged jets are reconstructed using tracks of charged particles (track-based jets) with the anti-kTk_{\mathrm{T}} algorithm in the jet transverse momentum range 5<pT,jetch<305<p_{\rm{T,jet}}^{\mathrm{ch}}<30 GeV/c{\rm GeV/}c and pseudorapidity ηjet<0.5|\eta_{\rm jet}|<0.5. The fraction of charged jets containing a D0^0-meson increases with pT,jetchp_{\rm{T,jet}}^{\rm{ch}} from 0.042±0.004(stat)±0.006(syst)0.042 \pm 0.004\, \mathrm{(stat)} \pm 0.006\, \mathrm{(syst)} to 0.080±0.009(stat)±0.008(syst)0.080 \pm 0.009\, \rm{(stat)} \pm 0.008\, \rm{(syst)}. The distribution of D0^0-meson tagged jets as a function of the jet momentum fraction carried by the D0^0 meson in the direction of the jet axis (zchz_{||}^{\mathrm{ch}}) is reported for two ranges of jet transverse momenta, 5<pT,jetch<155<p_{\rm{T,jet}}^{\rm{ch}}<15 GeV/c{\rm GeV/}c and 15<pT,jetch<3015<p_{\rm{T,jet}}^{\rm{ch}}<30 GeV/c{\rm GeV/}c in the intervals 0.2<zch<1.00.2<z_{||}^{\rm{ch}}<1.0 and 0.4<zch<1.00.4<z_{||}^{\rm{ch}}<1.0, respectively. The data are compared with results from Monte Carlo event generators (PYTHIA 6, PYTHIA 8 and Herwig 7) and with a Next-to-Leading-Order perturbative Quantum Chromodynamics calculation, obtained with the POWHEG method and interfaced with PYTHIA 6 for the generation of the parton shower, fragmentation, hadronisation and underlying event.Comment: 29 pages, 8 captioned figures, 3 tables, authors from page 24, published version, figures at http://alice-publications.web.cern.ch/node/525

    Thermal leptogenesis in a model with mass varying neutrinos

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    In this paper we consider the possibility of neutrino mass varying during the evolution of the Universe and study its implications on leptogenesis. Specifically, we take the minimal seesaw model of neutrino masses and introduce a coupling between the right-handed neutrinos and the dark energy scalar field, the Quintessence. In our model, the right-handed neutrino masses change as the Quintessence scalar evolves. We then examine in detail the parameter space of this model allowed by the observed baryon number asymmetry. Our results show that it is possible to lower the reheating temperature in this scenario in comparison with the case that the neutrino masses are unchanged, which helps solve the gravitino problem. Furthermore, a degenerate neutrino mass patten with mim_i larger than the upper limit given in the minimal leptogenesis scenario is permitted.Comment: 18 pages, 7 figures, version to appear in PR

    Neutrino masses and the number of neutrino species from WMAP and 2dFGRS

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    We have performed a thorough analysis of the constraints which can be put on neutrino parameters from cosmological observations, most notably those from the WMAP satellite and the 2dF galaxy survey. For this data we find an upper limit on the sum of active neutrino mass eigenstates of \sum m_nu < 1.0 eV (95% conf.), but this limit is dependent on priors. We find that the WMAP and 2dF data alone cannot rule out the evidence from neutrinoless double beta decay reported by the Heidelberg-Moscow experiment. In terms of the relativistic energy density in neutrinos or other weakly interacting species we find, in units of the equivalent number of neutrino species, N_nu, that N_nu = 4.0+3.0-2.1 (95% conf.). When BBN constraints are added, the bound on N_\nu is 2.6+0.4-0.3 (95% conf.), suggesting that N_nu could possibly be lower than the standard model value of 3. This can for instance be the case in models with very low reheating temperature and incomplete neutrino thermalization. Conversely, if N_nu is fixed to 3 then the data from WMAP and 2dFGRS predicts that 0.2458 < Y_P < 0.2471, which is significantly higher than the observationally measured value. The limit on relativistic energy density changes when a small νe\nu_e chemical potential is present during BBN. In this case the upper bound on N_nu from WMAP, 2dFGRS and BBN is N_nu < 6.5. Finally, we find that a non-zero \sum m_nu can be compensated by an increase in N_nu. One result of this is that the LSND result is not yet ruled out by cosmological observations.Comment: 10 pages, 6 figure

    Decoupling of Massive Right-handed Neutrinos

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    We investigate the effect of B+L - violating anomalous generation of massive right-handed neutrinos on their decoupling, when the right-handed neutrino mass is considerably greater than the right-handed gauge boson masses. Considering normal annihilation channels, the Lee-Weinberg type of calculation, in this case, gives an upper bound of about 700 Gev, which casts doubt on the existence of such a right-handed neutrino mass greater than right-handed gauge boson masses. We examine the possibility that a consideration of anomalous effects related to the SU(2)_R gauge group may turn this into a lower bound of the order of 100 Tev.Comment: 28 Pages, Latex, 2 figure

    Location, function, and nucleotide sequence of a promoter for bacteriophage T3 RNA polymerase

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    The major promoters for bacteriophage T3 RNA polymerase on the T3 genome have been mapped by DNA.RNA filter hybridization. One promoter is located in a 300-base-pair Hpa I restriction fragment near the genetic "left" end of T3 DNA. The sequence in the vicinity of the major initiation site of transcription in this region has been determined. A part of the (-)strand sequence is 5' T-A-T-T-T-A-C-C-C-T-C-A-C-T-A-A-A-G-+1 G-G-A-A-U 3'. Comparison of this sequence with the prototype 23-base-pair promoter sequence for bacteriophage T7 RNA polymerase shows a striking pattern of homology and divergence. Between positions -9 and +4, the sequences are virtually identical, whereas between positions -17 and -10, the sequences are quite different. It is postulated that these sequence subsets may perform different functions in transcription initiation by the phage RNA polymerases
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