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Pierre Auger Collaboration(Abraham, J. et al), & Pastor, S. (2010). Measurement of the Depth of Maximum of Extensive Air Showers above 10(18) eV. Phys. Rev. Lett., 104(9), 091101–7pp.
Abstract: We describe the measurement of the depth of maximum, X-max, of the longitudinal development of air showers induced by cosmic rays. Almost 4000 events above 10(18) eV observed by the fluorescence detector of the Pierre Auger Observatory in coincidence with at least one surface detector station are selected for the analysis. The average shower maximum was found to evolve with energy at a rate of (106 +/- 35-21) g/cm(2)/decade below 10(18.24) +/- (0.05) eV, and d24 +/- 3 g/cm(2)/ecade above this energy. The measured shower-to-shower fluctuations decrease from about 55 to 26 g/cm(2). The interpretation of these results in terms of the cosmic ray mass composition is briefly discussed.
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BABAR Collaboration(Aubert, B. et al), Azzolini, V., Lopez-March, N., Martinez-Vidal, F., Milanes, D. A., & Oyanguren, A. (2010). Measurement of vertical bar V-cb vertical bar and the Form-Factor Slope in (B)over-bar -> Dl(-) (nu)over-bar(l) Decays in Events Tagged by a Fully Reconstructed B Meson. Phys. Rev. Lett., 104(1), 011802–7pp.
Abstract: We present a measurement of the Cabibbo-Kobayashi-Maskawa matrix element vertical bar V-cb vertical bar and the form-factor slope rho(2) in (B) over bar -> Dl(-) (nu) over bar (l) decays based on 460 X 10(6) B (B) over bar events recorded at the Gamma(4S) resonance with the BABAR detector. (B) over bar -> Dl(-) (nu) over bar (l) decays are selected in events in which a hadronic decay of the second B meson is fully reconstructed. We measure B(B- -> D(0)l(-) (nu) over bar (l))/B(B- -> Xl(-) (nu) over bar (l)) = (0.255 +/- 0.009 +/- 0.009) and B((B) over bar (0) -> D(+)l(-) (nu) over bar (l))/B((B) over bar (0) -> Xl(-) (nu) over bar (l)) = (0.230 +/- 0.011 +/- 0.011), along with the differential decay distribution in (B) over bar -> Dl(-) (nu) over bar (l) decays. We then determine G(1)vertical bar V-cb vertical bar = 42.3 +/- 1.9 +/- 1.4) X 10(-3) and rho(2) = 1.20 +/- 0.09 +/- 0.04, where G(1) is the hadronic form factor at the point of zero recoil.
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BABAR Collaboration(Aubert, B. et al), Azzolini, V., Lopez-March, N., Martinez-Vidal, F., Milanes, D. A., & Oyanguren, A. (2010). Searches for Lepton Flavor Violation in the Decays tau(+/-) -> e(+/-)gamma and tau(+/-) -> mu(+/-)gamma. Phys. Rev. Lett., 104(2), 021802–7pp.
Abstract: Searches for lepton-flavor-violating decays of a tau lepton to a lighter mass lepton and a photon have been performed with the entire data set of (963 +/- 7) x 10(6) tau decays collected by the BABAR detector near the Y(4S), Y(3S) and Y(2S) resonances. The searches yield no evidence of signals and we set upper limits on the branching fractions of B(tau(+/-) -> e(+/-)gamma) < 3.3 X 10(-8) and B(tau(+/-) -> mu(+/-)gamma) < 4.4 X 10(-8) at 90% confidence level.
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Decoster, S., Cottenier, S., Wahl, U., Correia, J. G., Pereira, L. M. C., Lacasta, C., et al. (2010). Diluted manganese on the bond-centered site in germanium. Appl. Phys. Lett., 97(15), 151914–3pp.
Abstract: The functional properties of Mn-doped Ge depend to large extent on the lattice location of the Mn impurities. Here, we present a lattice location study of implanted diluted Mn by means of electron emission channeling. Surprisingly, in addition to the expected substitutional lattice position, a large fraction of the Mn impurities occupies the bond-centered site. Corroborated by ab initio calculations, the bond-centered Mn is related to Mn-vacancy complexes. These unexpected results call for a reassessment of the theoretical studies on the electrical and magnetic behavior of Mn-doped Ge, hereby including the possible role of Mn-vacancy complexes.
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Sanjuan, R., Nebot, M., Chirico, N., Mansky, L. M., & Belshaw, R. (2010). Viral Mutation Rates. J. Virol., 84(19), 9733–9748.
Abstract: Accurate estimates of virus mutation rates are important to understand the evolution of the viruses and to combat them. However, methods of estimation are varied and often complex. Here, we critically review over 40 original studies and establish criteria to facilitate comparative analyses. The mutation rates of 23 viruses are presented as substitutions per nucleotide per cell infection (s/n/c) and corrected for selection bias where necessary, using a new statistical method. The resulting rates range from 10(-8) to 10(-6) s/n/c for DNA viruses and from 10(-6) to 10(-4) s/n/c for RNA viruses. Similar to what has been shown previously for DNA viruses, there appears to be a negative correlation between mutation rate and genome size among RNA viruses, but this result requires further experimental testing. Contrary to some suggestions, the mutation rate of retroviruses is not lower than that of other RNA viruses. We also show that nucleotide substitutions are on average four times more common than insertions/deletions (indels). Finally, we provide estimates of the mutation rate per nucleotide per strand copying, which tends to be lower than that per cell infection because some viruses undergo several rounds of copying per cell, particularly double-stranded DNA viruses. A regularly updated virus mutation rate data set will be available at www.uv.es/rsanjuan/virmut.
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