184 research outputs found

    Neotenorchestia Wildish, 2014 is a junior synonym of Orchestia Leach, 1814

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    Neotenorchestia Wildish, 2014 and N. kenwildishi Wildish, 2014 (Crustacea, Amphipoda, Talitridae) are junior synonyms of Orchestia Leach, 1814 and Orchestia mediterranea A. Costa, 1853 respectively, based on revised genetic evidence

    A model of horse mussel reef formation in the Bay of Fundy based on population growth and geological processes

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    From a total of 14 geological sediment provinces recognized in the Bay of Fundy only five: sand with bioherms, gravel/cobble, gravel /scallop bed, mottled gravel and glacio-marine mud were found to have significant populations of the horse mussel, Modiolus modiolus. Valve increment measures of annual growth rings in the early years of life of populations of these Bay of Fundy horse mussels, suggest that growth rates vary with the geological province where they are found. Horse mussel populations grow fastest on sand with bioherms, closely followed by those growing on gravel/scallop bed; the slowest growing are found on gravel/ cobble and mottled gravel geological provinces. Multibeam bathymetry and backscatter data have been collected in an area of mussel reefs in the central part of the Bay of Fundy. The data indicates that the mussel reefs (bioherms) tend to occur on the eastern side of small, gravel covered, glacial ridges on the seabed and form a variety of single and multiple, long and short reefs that rise above the seabed up to 3 m high. They are always associated with sand in transport at the seabed in a variety of bedforms. A conceptual model of formation and location is presented that considers: current velocity and turbulence, well-mixed water masses, seabed morphology, sediment distribution and sediment transport, as causative factors. RÉSUMÉ D’un total de 14 classes de sédiments géologiques reconnues dans la baie de Fundy, seulement cinq (biohermes, gravier/galets, gravier/fond de pétoncle, gravier tacheté et boue glacio-marine) renfermaient des populations importantes de modiole Modiolus modiolus. Les mesures de l’augmentation valvaire des cernes d’accroissement annuels durant les premières années de vie des populations de modioles dans la baie de Fundy indiqueraient que les taux de croissance varient selon la classe de sédiment géologique où ils se trouvent. Les populations de modioles croissent plus rapidement dans le sable renfermant des biohermes, et la croissance est presque aussi grande chez les modioles présents dans les classes de sédiments composées de gravier/fond de pétoncles; la croissance la plus lente a été observée dans les classes de sédiments géologiques composées de gravier/galets et de gravier tacheté. Des données ont été recueillies au moyen de la bathymétrie par secteurs et de la rétrodiffusion dans une zone de récifs de moules de la partie centrale de la baie de Fundy. Les données indiquent que les récifs de moules (biohermes) semblent se former sur le côté est de petites crêtes glaciaires recouvertes de gravier sur le plancher sous‑marin, et qu’ils forment divers récifs uniques et multiples, longs et courts, qui s’élèvent sur le plancher sous-marin jusqu’à une hauteur de trois mètres. Ils sont toujours associés avec le sable déplacé sur le plancher sous-marin dans diverses morphologies de fond. On présente un modèle conceptuel de la formation et de l’emplacement qui considère comme facteurs de causalité les éléments suivants : la vitesse et la turbulence actuelles, les masses d’eau homogènes, la morphologie du plancher sous-marin, la répartition des sédiments et les transports sédimentaires. [Traduit par la redaction

    Performance of the CMS Cathode Strip Chambers with Cosmic Rays

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    The Cathode Strip Chambers (CSCs) constitute the primary muon tracking device in the CMS endcaps. Their performance has been evaluated using data taken during a cosmic ray run in fall 2008. Measured noise levels are low, with the number of noisy channels well below 1%. Coordinate resolution was measured for all types of chambers, and fall in the range 47 microns to 243 microns. The efficiencies for local charged track triggers, for hit and for segments reconstruction were measured, and are above 99%. The timing resolution per layer is approximately 5 ns

    Performance and Operation of the CMS Electromagnetic Calorimeter

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    The operation and general performance of the CMS electromagnetic calorimeter using cosmic-ray muons are described. These muons were recorded after the closure of the CMS detector in late 2008. The calorimeter is made of lead tungstate crystals and the overall status of the 75848 channels corresponding to the barrel and endcap detectors is reported. The stability of crucial operational parameters, such as high voltage, temperature and electronic noise, is summarised and the performance of the light monitoring system is presented

    First measurement of the quark-to-photon fragmentation function

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    Improved tau polarisation measurement

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    Production of excited beauty states in Z decays

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    A data sample of about 3.0 million hadronic Z decays collected by the ALEPH experiment at LEP in the years 1991 through 1994, is used to make an inclusive selection of B~hadron events. In this event sample 4227 \pm 140 \pm 252 B^* mesons in the decay B^* \to B \gamma and 1944 \pm 108 \pm 161 B^{**} mesons decaying into a B~meson and a charged pion are reconstructed. For the well established B^* meson the following quantities areobtained: \Delta M = M_{B^*} - M_{B} = (45.30\pm 0.35\pm 0.87)~\mathrm{MeV}/c^2 and N_{B^*}/(N_B+N_{B^*}) = (77.1 \pm 2.6 \pm 7.0)\%. The angular distribution of the photons in the B^* rest frame is used to measure the relative contribution of longitudinal B^* polarization states to be \sigma_L/(\sigma_L + \sigma_T)= (33 \pm 6 \pm 5)\%. \\ Resonance structure in the M(B\pi)-M(B) mass difference is observed at (424 \pm 4 \pm 10)~\mathrm{MeV}/c^2. Its shape and position is in agreement with the expectation for B^{**}_{u,d} states decaying into B_{u,d}^{(*)} \pi^\pm. The signal is therefore interpreted as arising from them. The relative production rate is determined to be \frac{BR(Z \to b \to B_{u,d}^{**})}{BR(Z \to b \to B_{u,d})} = [27.9 \pm 1.6(stat) \pm 5.9(syst) \phantom{a}^{+3.9}_{-5.6}(model)]\%. where the third error reflects the uncertainty due to different production and decay models for the broad B_{u,d}^{**} states

    Inclusive production of neutral vector mesons in hadronic Z decays

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    Tau hadronic branching ratios

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    From 64492 selected \tau-pair events, produced at the Z^0 resonance, the measurement of the tau decays into hadrons from a global analysis using 1991, 1992 and 1993 ALEPH data is presented. Special emphasis is given to the reconstruction of photons and \pi^0's, and the removal of fake photons. A detailed study of the systematics entering the \pi^0 reconstruction is also given. A complete and consistent set of tau hadronic branching ratios is presented for 18 exclusive modes. Most measurements are more precise than the present world average. The new level of precision reached allows a stringent test of \tau-\mu universality in hadronic decays, g_\tau/g_\mu \ = \ 1.0013 \ \pm \ 0.0095, and the first measurement of the vector and axial-vector contributions to the non-strange hadronic \tau decay width: R_{\tau ,V} \ = \ 1.788 \ \pm \ 0.025 and R_{\tau ,A} \ = \ 1.694 \ \pm \ 0.027. The ratio (R_{\tau ,V} - R_{\tau ,A}) / (R_{\tau ,V} + R_{\tau ,A}), equal to (2.7 \pm 1.3) \ \%, is a measure of the importance of QCD non-perturbative contributions to the hadronic \tau decay widt

    Measurement of the tau lepton lifetime

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    The mean lifetime of the tau lepton is measured in a sample of 25700 tau pairs collected in 1992 with the ALEPH detector at LEP. A new analysis of the 1-1 topology events is introduced. In this analysis, the dependence of the impact parameter sum distribution on the daughter track momenta is taken into account, yielding improved precision compared to other impact parameter sum methods. Three other analyses of the one- and three-prong tau decays are updated with increased statistics. The measured lifetime is 293.5+/-3.1+/-1.7 fs. Including previous (1989-1991) ALEPH measurements, the combined tau lifetime is 293.7+/-2.7+/-1.6 fs
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