35,211 research outputs found

    Bose-Einstein condensate of kicked rotators with time-dependent interaction

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    A modification of the quantum kicked rotator is suggested with a time-dependent delta-kicked interaction parameter which can be realized by a pulsed turn-on of a Feshbach resonance. The mean kinetic energy increases exponentially with time in contrast to a merely diffusive or linear growth for the first few kicks for the quantum kicked rotator with a constant interaction parameter. A recursive relation is derived in a self-consistent random phase approximation which describes this superdiffusive growth of the kinetic energy and is compared with numerical simulations. Unlike in the case of the quantum rotator with constant interaction, a Lax pair is not found. In general the delta-kicked interaction is found to lead to strong chaotic behaviour.Comment: 4 pages, 3 figure

    Damage Spreading During Domain Growth

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    We study damage spreading in models of two-dimensional systems undergoing first order phase transitions. We consider several models from the same non-conserved order parameter universality class, and find unexpected differences between them. An exact solution of the Ohta-Jasnow-Kawasaki model yields the damage growth law D∼tϕD \sim t^{\phi}, where ϕ=td/4\phi = t^{d/4} in dd dimensions. In contrast, time-dependent Ginzburg-Landau simulations and Ising simulations in d=2d= 2 using heat-bath dynamics show power-law growth, but with an exponent of approximately 0.360.36, independent of the system sizes studied. In marked contrast, Metropolis dynamics shows damage growing via ϕ∼1\phi \sim 1, although the damage difference grows as t0.4t^{0.4}. PACS: 64.60.-i, 05.50.+qComment: 4 pags of revtex3 + 3 postscript files appended as a compressed and uuencoded file. UIB940320

    Equilibrium Distribution of Heavy Quarks in Fokker-Planck Dynamics

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    We obtain within Fokker-Planck dynamics an explicit generalization of Einstein's relation between drag, diffusion and equilibrium distribution for a spatially homogeneous system, considering both the transverse and longitudinal diffusion for dimension n>1. We then provide a complete characterization of when the equilibrium distribution becomes a Boltzmann/J"uttner distribution, and when it satisfies the more general Tsallis distribution. We apply this analysis to recent calculations of drag and diffusion of a charm quark in a thermal plasma, and show that only a Tsallis distribution describes the equilibrium distribution well. We also provide a practical recipe applicable to highly relativistic plasmas, for determining both diffusion coefficients so that a specific equilibrium distribution will arise for a given drag coefficient.Comment: 4 pages including 2 figure

    A SQUAMOSA MADS-box gene involved in the regulation of anthocyanin accumulation in bilberry fruits

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    Anthocyanins are important health promoting phytochemicals that are abundant in many fleshy fruits. Bilberry (Vaccinium myrtillus L.) is one of the best sources of these compounds. Here we report on the expression pattern and functional analysis of a SQUAMOSA (SQUA) class MADS-box transcription factor, VmTDR4, associated with anthocyanin biosynthesis in bilberry. Levels of VmTDR4 expression were spatially and temporally linked with colour development and anthocyanin-related gene expression. Virus induced gene silencing (VIGS) was used to suppress VmTDR4 expression in bilberry resulting in substantial reduction in anthocyanin levels in fully ripe fruits. Chalcone synthase was used a positive control in the VIGS experiments. Additionally, in sectors of fruit tissue in which the expression of the VmTDR4 gene was silenced, the expression of R2R3 MYB family transcription factors related to the biosynthesis of flavonoids were also altered. We conclude that VmTDR4 plays an important role in the accumulation of anthocyanins during normal ripening in bilberry; probably through direct or indirect control of transcription factors belonging to the R2R3 MYB family

    The Cellular Metabolism and Effects of Gold Complexes

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    Leads to the cellular effects of the anti-arthritic gold complexes may come from the determination of their metabolism by target cells and, possibly, cells in the immediate environment of the target cells. Polymorphonuclear leukocytes (PMN) and mononuclear cells (monocytes and lymphocytes) are present in inflamed joints of patients with rheumatoid arthritis and these cells have been widely used in pharmacological studies on the gold complexes. It is suggested that the cellular effects of the gold complexes are mediated by the production of aurocyanide. According to this hypothesis, PMN metabolize small quantities of thiocyanate to cyanide which, in turn, converts gold complexes, such as aurothiomalate, to aurocyanide (dicyanogold(I)) which inhibits the functions of PMN and other cells. There is now considerable evidence for this hypothesis from in vitro studies but there is little in vivo work to back up the hypothesis. One of the few in vivo studies which tested the hypothesis involved the examination of the activity of aurothiomalate in the treatment of polyarthritis in Hooded Wistar rats. Activity of aurothiomalate is only shown in animals which received thiocyanate. Hydrogen cyanide is a constituent of cigarette smoke and the aurocyanide formed by the interaction with gold complexes and inhaled hydrogen cyanide rapidly diffuses into red blood cells. Because of the metabolism of hydrogen cyanide to thiocyanate in the liver, there are higher plasma levels of thiocyanate in smokers than in non-smokers. Smokers may have a greater incidence of side effects than non-smokers but there appears to be little difference in therapeutic response, possibly because there is sufficient thiocyanate in extracellular fluid, even in non-smokers, to support the conversion of gold complexes to aurocyanide. The relationship between the metabolism and effects of the orally active gold complex, auranofin are less clear. Auranofin itself is taken up by cells with the loss of the ligands bound to gold while its inhibitory activity against the oxidative burst of PMN decreases with increasing cell density. For example, the lucigenin-dependent chemiluminescence of 106 PMN/ml is 46 percent of control at 0.5 μM auranofin but only 2.2 percent in 2.105 PMN/ml in the presence of the same concentration of auranofin. A potentially active gold complex is a plasma component which is taken up by red blood cells

    Casimir Forces between Compact Objects: I. The Scalar Case

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    We have developed an exact, general method to compute Casimir interactions between a finite number of compact objects of arbitrary shape and separation. Here, we present details of the method for a scalar field to illustrate our approach in its most simple form; the generalization to electromagnetic fields is outlined in Ref. [1]. The interaction between the objects is attributed to quantum fluctuations of source distributions on their surfaces, which we decompose in terms of multipoles. A functional integral over the effective action of multipoles gives the resulting interaction. Each object's shape and boundary conditions enter the effective action only through its scattering matrix. Their relative positions enter through universal translation matrices that depend only on field type and spatial dimension. The distinction of our method from the pairwise summation of two-body potentials is elucidated in terms of the scattering processes between three objects. To illustrate the power of the technique, we consider Robin boundary conditions ϕ−λ∂nϕ=0\phi -\lambda \partial_n \phi=0, which interpolate between Dirichlet and Neumann cases as λ\lambda is varied. We obtain the interaction between two such spheres analytically in a large separation expansion, and numerically for all separations. The cases of unequal radii and unequal λ\lambda are studied. We find sign changes in the force as a function of separation in certain ranges of λ\lambda and see deviations from the proximity force approximation even at short separations, most notably for Neumann boundary conditions.Comment: 27 pages, 9 figure
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