Non-perturbative structure of the polarized nucleon sea

We investigate the flavour and quark-antiquark structure of the polarized nucleon by calculating the parton distribution functions of the nucleon sea using the meson cloud model. We find that the SU(2) flavor symmetry in the light antiquark sea and quark-antiquark symmetry in the strange quark sea are broken, {\it i.e.} \Delta\ubar < \Delta \dbar and \Delta s < \Delta \sbar. The polarization of the strange sea is found to be positive, which is in contradiction to previous analyses. We predict a much larger quark-antiquark asymmetry in the polarized strange quark sea than that in the unpolarized strange quark sea. Our results for both polarized light quark sea and polarized strange quark sea are consistent with the recent HERMES data.Comment: RevTex, 17 pages plus 8 PS figure

Perturbative and nonperturbative contributions to the strange quark asymmetry in the nucleon

There are two mechanisms for the generation of an asymmetry between the strange and anti-strange quark distributions in the nucleon: nonperturbative contributions originating from nucleons fluctuating into virtual baryon-meson pairs such as $\Lambda K$ and $\Sigma K$, and perturbative contributions arising from gluons splitting into strange and anti-strange quark pairs. While the nonperturbative contributions are dominant in the large-$x$ region, the perturbative contributions are more significant in the small-$x$ region. We calculate this asymmetry taking into account both nonperturbative and perturbative contributions, thus giving a more accurate evaluation of this asymmetry over the whole domain of $x$. We find that the perturbative contributions are generally a few times larger in magnitude than the nonperturbative contributions, which suggests that the best region to detect this asymmetry experimentally is in the region $0.02 < x < 0.03$. We find that the asymmetry may have more than one node, which is an effect that should be taken into account, e.g. for parameterizations of the strange and anti-strange quark distributions used in global analysis of parton distributions.Comment: 14 pages, 4 figures, figures comparing theoretical calculations with NNPDF global analysis added, accepted for publication in EPJ

Measurement of Z0 decays to hadrons, and a precise determination of the number of neutrino species

We have made a precise measurement of the cross section for e+e---&gt;Z0--&gt;hadrons with the L3 detector at LEP, covering the range from 88.28 to 95.04 GeV. From a fit to the Z0 mass, total width, and the hadronic cross section to be MZ0=91.160 +/- 0.024 (experiment) +/-0.030(LEP) GeV, [Gamma]Z0=2.539+/-0.054 GeV, and [sigma]h(MZ0)=29.5+/-0.7 nb. We also used the fit to the Z0 peak cross section and the width todetermine [Gamma]invisible=0.548+/-0.029 GeV, which corresponds to 3.29+/-0.17 species of light neutrinos. The possibility of four or more neutrino flavors is thus ruled out at the 4[sigma] confidence level.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/28683/3/0000500.pd

A measurement of the Z0 leptonic partial widths and the vector and axial vector coupling constants

We have measured the partial widths of the Z0 into lepton pairs, and the forward-backward charge asymmetry for the process e+e---&gt;[mu]+[mu]- using the L3 detector at LEP. We obtain an average [Gamma]ll of 83.0+/-2.1+/-1.1 MeV.From this result and the asymmetry measurement, we extract the values of the vector and axial vector couplings of the Z0 to leptons: grmv=-0.066-0.027+0.046 and grmA= -0.495-0.007+0.007.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/28666/3/0000483.pd

Regulation of adhesion by flexible ectodomains of IgCAMs

To perform their diverse biological functions the adhesion activities of the cell adhesion molecules of the immunoglobulin superfamily (IgCAMs) might be regulated by local clustering, proteolytical shedding of their ectodomains or rapid recycling to and from the plasma membrane. Another form of regulation of adhesion might be obtained through flexible ectodomains of IgCAMs which adopt distinct conformations and which in turn modulate their adhesion activity. Here, we discuss variations in the conformation of the extracellular domains of CEACAM1 and CAR that might influence their binding and signaling activities. Furthermore, we concentrate on alternative splicing of single domains and short segments in the extracellular regions of L1 subfamily members that might affect the organization of the N-terminal located Ig-like domains. In particular, we discuss variations of the linker sequence between Ig-like domains 2 and 3 (D2 and D3) that is required for the horseshoe conformation

Partially open grain and phase boundaries as fluid pathways in metamorphic and magmatic rocks

Transmission electron microscopy and 3D focused ion beam/scanning electron microscope nanotomography are applied to grain and phase boundaries between quartz, plagioclase, K-feldspar, clinopyroxene, amphibole, and calcite. The samples come from metamorphic, plutonic and volcanic rocks, and hydrothermal quartz, and experienced cooling and decompression after highly variable P–T peak conditions. Most of the boundaries are partially open in the range of up to several hundred nanometres and partly to totally filled with secondary minerals, such as actinolite, biotite, chlorite, sheet silicates, and quartz, as well as with amorphous matter. Cracking and opening of boundaries are suggested to be related to anisotropic thermoelastic response of crystals to cooling. It starts below the brittle–ductile transition of the involved minerals. The partially open grain and phase boundaries, together with dissolution-generated cavities, can form porosity of more than 2 vol.% and permeability under conditions of at least lowermost greenschist facies. Such networks of partially open or partially refilled boundaries potentially affect properties of crystalline rocks and processes in the upper crust, such as metasomatism, weathering, migration of radionuclides through bedrock of geological repositories of nuclear waste, and deformation in nature and in experiment.ISSN:0263-4929ISSN:1525-131

The coxsackievirus adenovirus receptor reveals complex homophilic and heterophilic interactions on neural cells

The coxsackievirus-adenovirus receptor (CAR) is a member of the Ig superfamily strongly expressed in the developing nervous system. Our histological investigations during development reveal an initial uniform distribution of CAR on all neural cells with a concentration on membranes that face the margins of the nervous system (e.g., the basal laminae and the ventricular side). At more advanced stages, CAR becomes downregulated and restricted to specific regions including areas rich in axonal and dendritic surfaces. To study the function of CAR on neural cells, we used the fiber knob of the adenovirus, extracellular CAR domains, blocking antibodies to CAR, as well as CAR-deficient neural cells. Blocking antibodies were found to inhibit neurite extension in retina organ and retinal explant cultures, whereas the application of the recombinant fiber knob of the adenovirus subtype Ad2 or extracellular CAR domains promoted neurite extension and adhesion to extracellular matrices. We observed a promiscuous interaction of CAR with extracellular matrix glycoproteins, which was deduced from analytical ultracentrifugation experiments, affinity chromatography, and adhesion assays. The membrane proximal Ig domain of CAR, termed D2, was found to bind to a fibronectin fragment, including the heparin-binding domain 2, which promotes neurite extension of wild type, but not of CAR-deficient neural cells. In contrast to heterophilic interactions, homophilic association of CAR involves both Ig domains, as was revealed by ultracentrifugation, chemical cross-linking, and adhesion studies. The results of these functional and binding studies are correlated to a U-shaped homodimer of the complete extracellular domains of CAR detected by x-ray crystallography

Inhibition of phosphodiesterase 2 increases neuronal cGMP, synaptic plasticity and memory performance

An essential element of the signalling cascade leading to synaptic plasticity is the intracellular second messenger molecule guanosine 3¿,5¿-cyclic monophosphate (cGMP). Using the novel, potent, and selective inhibitor Bay 60-7550, we show that the enzyme 3¿,5¿-cyclic nucleotide phosphodiesterase type 2 (PDE2) is responsible for the degradation of newly synthesized cGMP in cultured neurons and hippocampal slices. Inhibition of PDE2 enhanced long-term potentiation of synaptic transmission without altering basal synaptic transmission. Inhibition of PDE2 also improved the performance of rats in social and object recognition memory tasks, and reversed MK801-induced deficits in spontaneous alternation in mice in a T-maze. Our data provide strong evidence that inhibition of PDE2 can improve memory functions by enhancing neuronal plasticit