1,068 research outputs found

    Data sources for rescuing the rich heritage of Mediterranean historical surface climate data

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    10.1002/gdj3.4Availability of long-term and high-quality instrumental climate records is still insufficient and the rich heritage of meteorological surface observations is largely underexploited in many parts of the world. This is particularly striking over the Greater Mediterranean region (GMR), where meteorological observations have been taken since the 18th century at some locations. The lack of high quality and long series here is despite this region being regarded as a climate change hot spot. This article mainly assesses relevant sources containing Mediterranean historical climate data and metadata either from online repositories worldwide or physical archives, with the emphasis here on the rich holdings kept at French archives. A particular case study is the data rescue (DARE) program undertaken by the Algerian National Meteorological Service, as well as some of the past and ongoing projects and initiatives aimed at enhancing climate data availability and accessibility over the GMR. Our findings point to the high potential for undertaking DARE activities over the GMR and the need for bringing longer and higher quality climate time series to support a diverse number of scientific and technical assessments and policies

    Rates for the reactions antiproton-proton --> pi phi and gamma phi

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    We study antiproton-proton annihilation at rest into πϕ\pi\phi and γϕ\gamma\phi. Rescattering by KK+KK\overline{K^*}K+K^*\overline{K} and ρ+ρ\rho^{+}\rho^{-} for ppπϕ\overline{p}p\rightarrow\pi\phi states is sizable, of order (0.90to2.6)×104(0.90\, {\rm to}\,2.6)\times 10^{-4} in the branching ratio, but smaller than experiment. For ppγϕ\overline{p}p\rightarrow\gamma\phi the rescattering contributions are negligible, but the γϕ\gamma\phi channel is well explained by a ρϕ\rho\phi intermediate state combined with vector meson dominance.Comment: 12 pages, plain latex, 2 postscript figures available upon request, PSI-PR-93-2

    Universal Scaling of Wave Propagation Failure in Arrays of Coupled Nonlinear Cells

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    We study the onset of the propagation failure of wave fronts in systems of coupled cells. We introduce a new method to analyze the scaling of the critical external field at which fronts cease to propagate, as a function of intercellular coupling. We find the universal scaling of the field throughout the range of couplings, and show that the field becomes exponentially small for large couplings. Our method is generic and applicable to a wide class of cellular dynamics in chemical, biological, and engineering systems. We confirm our results by direct numerical simulations.Comment: 4 pages, 3 figures, RevTe

    Branching Ratio and CP Asymmetry of B_s \to K^*_0(1430)\pi Decays in the PQCD Approach

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    In the two-quark model supposition for K0(1430)K_0^{*}(1430), the branching ratios and the direct CP-violating asymmetries for decays Bˉs0K00(1430)π0,K0+(1430)π\bar B_s^0\to K^{*0}_0(1430)\pi^0, K^{*+}_0(1430)\pi^- are studied by employing the perturbative QCD factorization approach. We find that although these two decays are both tree-dominated, the ratio of their penguin to tree contributions are very different: there is only a few percent for the decay Bˉs0K0+(1430)π\bar B_s^0\to K^{*+}_0(1430)\pi^-, while about 37% in scenario I, even 51% in scenario II for the decay Bˉs0K00(1430)π0\bar B_s^0\to K^{*0}_0(1430)\pi^0. It results that these two decays have very different values in the branching ratios and the direct CP asymmetries. The branching ratio of the decay Bˉs0K0+(1430)π\bar B_s^0\to K^{*+}_0(1430)\pi^- is at the order of 10510^{-5}, and its direct CP asymmetry is about (20-30)%. While for the decay Bˉs0K00(1430)π0\bar B_s^0\to K^{*0}_0(1430)\pi^0, its direct CP-violating asymmetry is very large and about 90%, but it is difficult to measure it, because the branching ratio for this channel is small and only 10710^{-7} order.Comment: 8pages, 2figure

    Clustering and Sharing Incentives in BitTorrent Systems

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    Peer-to-peer protocols play an increasingly instrumental role in Internet content distribution. Consequently, it is important to gain a full understanding of how these protocols behave in practice and how their parameters impact overall performance. We present the first experimental investigation of the peer selection strategy of the popular BitTorrent protocol in an instrumented private torrent. By observing the decisions of more than 40 nodes, we validate three BitTorrent properties that, though widely believed to hold, have not been demonstrated experimentally. These include the clustering of similar-bandwidth peers, the effectiveness of BitTorrent's sharing incentives, and the peers' high average upload utilization. In addition, our results show that BitTorrent's new choking algorithm in seed state provides uniform service to all peers, and that an underprovisioned initial seed leads to the absence of peer clustering and less effective sharing incentives. Based on our observations, we provide guidelines for seed provisioning by content providers, and discuss a tracker protocol extension that addresses an identified limitation of the protocol

    Linguistic expert creation in online health practices

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    In this chapter, we explore how the construction of an expert identity varies across online e-health settings with different socio-technological features. Our methodology is qualitative in nature and draws on insights from discourse analysis, in particular positioning theory. Results show that four aspects of creating expertise are vital: the embeddedness of the posi-tioning strategies in the online health context, the interplay between these strategies within each setting, the interactivity of the medium, and the fact that not only professionals, but also clients and laypeople construct their expertise. The results reveal that previously found strategies to create expertise (e.g., using jargon or showing empathy) could be confirmed in our corpus, and that the interplay of several strategies is in fact needed to create credible and trustworthy expert identities for all participants involved. This interplay varies accord-ing to the practice

    The detailed mechanism of the eta production in pp scattering up to the Tlab = 4.5 GeV

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    Contrary to very early beliefs, the experimental cross section data for the eta production in proton-proton scattering are well described if pi and only eta meson exchange diagrams are used to calculate the Born term. The inclusion of initial and final state interactions is done in the factorization approximation by using the inverse square of the Jost function. The two body Jost functions are obtained from the S matrices in the low energy effective range approximation. The danger of double counting in the p-eta final state interaction is discussed. It is shown that higher partial waves in meson-nucleon amplitudes do not contribute significantly bellow excess energy of Q=100 MeV. Known difficulties of reducing the multi resonance model to a single resonance one are illustrated.Comment: 10 pages, 5 figures, corrected typos in relation (3), changed content (added section with differential cross sections

    Mutations in the C-terminal region of the HIV-1 reverse transcriptase and their correlation with drug resistance associated mutations and antiviral treatment

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    <p>Abstract</p> <p>Objective</p> <p>Replication of HIV-1 after cell entry is essentially dependent on the reverse transcriptase (RT). Antiretroviral drugs impairing the function of the RT currently aim at the polymerase subunit. One reason for failure of antiretroviral treatment is the evolvement of resistance-associated mutations in the viral genome. For RT inhibitors, almost all identified mutations are located within the polymerase; therefore, general genotyping confines to investigate this subunit. Recently several studies have shown that substitutions within the RNase H and the connection domain increase antiviral drug-resistance in vitro, and some of them are present in patient isolates.</p> <p>Aim</p> <p>The aim of the present study was to investigate the prevalence of these substitutions and their association with mutations in the polymerase domain arising during antiretroviral treatment.</p> <p>Materials and methods</p> <p>We performed genotypic analyzes on seventy-four virus isolates derived from treated and untreated patients, followed at the HIV Centre of the Johann Wolfgang Goethe University Hospital (Frankfurt/Main, Germany). We subsequently analysed the different substitutions in the c-terminal region to evaluate whether there were associations with each other, n-terminal substitutions or with antiretroviral treatment.</p> <p>Results</p> <p>We identified several primer grip substitutions, but almost all of them were located in the connection domain. This is consistent with other in-vivo studies, in which especially the primer grip residues located in the RNase H were unvaried. Furthermore, we identified other substitutions in the connection domain and in the RNase H. Especially E399D seemed to be associated with an antiretroviral treatment and N-terminal resistance-delivering mutations.</p> <p>Conclusion</p> <p>Some of the identified substitutions were associated with antiviral treatment and drug resistance-associated mutations. Due to the low prevalence of C-terminal mutations and as only a few of them could be associated with antiviral treatment and N-terminal resistance-delivering mutations, we would not recommend routinely testing of the C-terminal RT region.</p
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