248 research outputs found
Meson Decay Constants from Isospin Mass Splittings in the Quark Model
Decay constants of and mesons are estimated within the framework of a
heavy-quark approach using measured isospin mass splittings in the , ,
and states to isolate the electromagnetic hyperfine interaction between
quarks. The values MeV and MeV are
obtained. Only experimental errors are given; possible theoretical ambiguities,
and suggestions for reducing them, are noted.Comment: 7 pages, LaTeX, EFI-92-3
Deep inelastic production at HERA in the -factorization approach and its consequences for the nonrelativistic QCD
In the framework of the -factorization approach, we analyse the
inclusive and inelastic production of particles in deep inelastic
scattering. We take into account both colour-singlet and colour-octet
production channels. We inspect the sensitivity of theoretical predictions to
the choice of model parameters. Our theoretical results agree reasonably well
with recent experimental data collected by the collaboration H1 at HERA.Comment: 14 pages, 6 figure
Upsilonium polarization as a touchstone in understanding the proton dynamics in QCD
In the framework of the k_t-factorization approach, the production of
\alpha$ are presented. We argue
that measuring the polarization of quarkonium states can serve as a crucial
test discriminating two competing theoretical approaches to parton dynamics in
QCD.Comment: 8 pages, 2 figure
Possible Explanation Why \tau_{B^{\pm}}\sim\tau_{B^0} But \tau_{D^{\pm}}\sim \tau_{D^0}
Data show that \tau_{B^{\pm}}\sim\tau_{B^0}, but \tau_{D^{\pm}}\sim
2\tau_{D^0}. The naive interpretation which attributes \tau_{D^{\pm}}\sim
2\tau_{D^0} to a destructive interference between two quark diagrams for
D^{\pm} decays, definitely fails in the B-case. We investigate Close and
Lipkin's suggestion that the phases for producing radially excited states
\psi_{2s} in the decay products of B-mesons can possess an opposite sign to the
integrals for \psi_{1s} decay products. Their contributions can partially
compensate each other to result in \tau_{B^{\pm}}\sim\tau_{B^0}. Since D-mesons
are much lighter than B-mesons, such possibilities do not exist in D-decays.Comment: 14 pages, latex, 4 ps figures. to appear in Phys. Rev.
Leptonic and Semileptonic Decays of Charm and Bottom Hadrons
We review the experimental measurements and theoretical descriptions of
leptonic and semileptonic decays of particles containing a single heavy quark,
either charm or bottom. Measurements of bottom semileptonic decays are used to
determine the magnitudes of two fundamental parameters of the standard model,
the Cabibbo-Kobayashi-Maskawa matrix elements and . These
parameters are connected with the physics of quark flavor and mass, and they
have important implications for the breakdown of CP symmetry. To extract
precise values of and from measurements, however,
requires a good understanding of the decay dynamics. Measurements of both charm
and bottom decay distributions provide information on the interactions
governing these processes. The underlying weak transition in each case is
relatively simple, but the strong interactions that bind the quarks into
hadrons introduce complications. We also discuss new theoretical approaches,
especially heavy-quark effective theory and lattice QCD, which are providing
insights and predictions now being tested by experiment. An international
effort at many laboratories will rapidly advance knowledge of this physics
during the next decade.Comment: This review article will be published in Reviews of Modern Physics in
the fall, 1995. This file contains only the abstract and the table of
contents. The full 168-page document including 47 figures is available at
http://charm.physics.ucsb.edu/papers/slrevtex.p
Infectivity in Skeletal Muscle of Cattle with Atypical Bovine Spongiform Encephalopathy
The amyloidotic form of bovine spongiform encephalopathy (BSE) termed BASE is caused by a prion strain whose biological properties differ from those of typical BSE, resulting in a clinically and pathologically distinct phenotype. Whether peripheral tissues of BASE-affected cattle contain infectivity is unknown. This is a critical issue since the BASE prion is readily transmissible to a variety of hosts including primates, suggesting that humans may be susceptible. We carried out bioassays in transgenic mice overexpressing bovine PrP (Tgbov XV) and found infectivity in a variety of skeletal muscles from cattle with natural and experimental BASE. Noteworthy, all BASE muscles used for inoculation transmitted disease, although the attack rate differed between experimental and natural cases (∼70% versus ∼10%, respectively). This difference was likely related to different prion titers, possibly due to different stages of disease in the two conditions, i.e. terminal stage in experimental BASE and pre-symptomatic stage in natural BASE. The neuropathological phenotype and PrPres type were consistent in all affected mice and matched those of Tgbov XV mice infected with brain homogenate from natural BASE. The immunohistochemical analysis of skeletal muscles from cattle with natural and experimental BASE showed the presence of abnormal prion protein deposits within muscle fibers. Conversely, Tgbov XV mice challenged with lymphoid tissue and kidney from natural and experimental BASE did not develop disease. The novel information on the neuromuscular tropism of the BASE strain, efficiently overcoming species barriers, underlines the relevance of maintaining an active surveillance
Prion protein-specific antibodies that detect multiple TSE agents with high sensitivity
This paper describes the generation, characterisation and potential applications of a panel of novel anti-prion protein monoclonal antibodies (mAbs). The mAbs were generated by immunising PRNP null mice, using a variety of regimes, with a truncated form of recombinant ovine prion protein spanning residues 94–233. Epitopes of specific antibodies were mapped using solid-phase Pepscan analysis and clustered to four distinct regions within the PrP molecule. We have demonstrated the utility of these antibodies by use of Western blotting and immunohistochemistry in tissues from a range of different species affected by transmissible spongiform encephalopathy (TSE). In comparative tests against extensively-used and widely-published, commercially available antibodies, similar or improved results can be obtained using these new mAbs, specifically in terms of sensitivity of detection. Since many of these antibodies recognise native PrPC, they could also be applied to a broad range of immunoassays such as flow cytometry, DELFIA analysis or immunoprecipitation. We are using these reagents to increase our understanding of TSE pathogenesis and for use in potential diagnostic screening assays
Business Constraints and Growth Potential of Micro and Small Manufacturing Enterprises in Uganda
Business constraints and growth potential of micro and small manufacturing enterprises in Uganda
Ugandan micro and small enterprises (MSEs) still perform poorly. Studies associating poor performance of manufacturers with lack of finance and low investment ignore micro enterprises. Those focusing on MSEs are either exploratory in nature or employ a descriptive analysis, which cannot show the extent to which business constraints explain the performance of MSEs. Thus, this paper tries to examine the extent to which the growth of MSEs is associated with business constraints while controlling for owners’ attributes and firms’ characteristics. The results reveal that MSEs’ growth potential is negatively associated with limited access to productive resources (finance and business development services), high taxes and lack of market access
Ecological networks: Pursuing the shortest path, however narrow and crooked
International audienceRepresenting data as networks cuts across all sub-disciplines in ecology and evolutionary biology. Besides providing a compact representation of the interconnections between agents, network analysis allows the identification of especially important nodes, according to various metrics that often rely on the calculation of the shortest paths connecting any two nodes. While the interpretation of a shortest paths is straightforward in binary, unweighted networks, whenever weights are reported, the calculation could yield unexpected results. We analyzed 129 studies of ecological networks published in the last decade that use shortest paths, and discovered a methodological inaccuracy related to the edge weights used to calculate shortest paths (and related centrality measures), particularly in interaction networks. Specifically, 49% of the studies do not report sufficient information on the calculation to allow their replication, and 61% of the studies on weighted networks may contain errors in how shortest paths are calculated. Using toy models and empirical ecological data, we show how to transform the data prior to calculation and illustrate the pitfalls that need to be avoided. We conclude by proposing a five-point checklist to foster best-practices in the calculation and reporting of centrality measures in ecology and evolution studies. The last two decades have witnessed an exponential increase in the use of graph analysis in ecological and conservation studies (see refs. 1,2 for recent introductions to network theory in ecology and evolution). Networks (graphs) represent agents as nodes linked by edges representing pairwise relationships. For instance, a food web can be represented as a network of species (nodes) and their feeding relationships (edges) 3. Similarly, the spatial dynamics of a metapopulation can be analyzed by connecting the patches of suitable habitat (nodes) with edges measuring dispersal between patches 4. Data might either simply report the presence/absence of an edge (binary, unweighted networks), or provide a strength for each edge (weighted networks). In turn, these weights can represent a variety of ecologically-relevant quantities, depending on the system being described. For instance, edge weights can quantify interaction frequency (e.g., visitation networks 5), interaction strength (e.g., per-capita effect of one species on the growth rate of another 3), carbon-flow between trophic levels 6 , genetic similarity 7 , niche overlap (e.g., number of shared resources between two species 8), affinity 9 , dispersal probabilities (e.g., the rate at which individuals of a population move between patches 10), cost of dispersal between patches (e.g., resistance 11), etc. Despite such large variety of ecological network representations, a common task is the identification of nodes of high importance, such as keystone species in a food web, patches acting as stepping stones in a dispersal network , or genes with pleiotropic effects. The identification of important nodes is typically accomplished through centrality measures 5,12. Many centrality measures has been proposed, each probing complementary aspects of node-to-node relationships 13. For instance, Closeness centrality 14,15 highlights nodes that are "near" to all othe
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