36,403 research outputs found

    Stochastic and Discrete Time Models of Long-Range Turbulent Transport in the Scrape-Off Layer

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    Two dimensional stochastic time model of scrape-off layer (SOL) turbulent transport is studied. Instability arisen in the system with respect to the stochastic perturbations of both either density or vorticity reveals itself in the strong outward bursts of particle density propagating ballistically across the SOL. The stability and possible stabilization of the cross- field turbulent system depend very much upon the reciprocal correlation time between density and vorticity fluctuations. Pdf of the particle flux for the large magnitudes of flux events can be modelled with a simple discrete time toy model of random walks concluding at a boundary. The spectra of wandering times feature the pdf of particle flux in the model and qualitatively reproduce the experimental statistics of transport events.Comment: 21 pages,11 figure

    Homogeneous and Scalable Gene Expression Regulatory Networks with Random Layouts of Switching Parameters

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    We consider a model of large regulatory gene expression networks where the thresholds activating the sigmoidal interactions between genes and the signs of these interactions are shuffled randomly. Such an approach allows for a qualitative understanding of network dynamics in a lack of empirical data concerning the large genomes of living organisms. Local dynamics of network nodes exhibits the multistationarity and oscillations and depends crucially upon the global topology of a "maximal" graph (comprising of all possible interactions between genes in the network). The long time behavior observed in the network defined on the homogeneous "maximal" graphs is featured by the fraction of positive interactions (0≤η≤10\leq \eta\leq 1) allowed between genes. There exists a critical value ηc<1\eta_c<1 such that if η<ηc\eta<\eta_c, the oscillations persist in the system, otherwise, when η>ηc,\eta>\eta_c, it tends to a fixed point (which position in the phase space is determined by the initial conditions and the certain layout of switching parameters). In networks defined on the inhomogeneous directed graphs depleted in cycles, no oscillations arise in the system even if the negative interactions in between genes present therein in abundance (ηc=0\eta_c=0). For such networks, the bidirectional edges (if occur) influence on the dynamics essentially. In particular, if a number of edges in the "maximal" graph is bidirectional, oscillations can arise and persist in the system at any low rate of negative interactions between genes (ηc=1\eta_c=1). Local dynamics observed in the inhomogeneous scalable regulatory networks is less sensitive to the choice of initial conditions. The scale free networks demonstrate their high error tolerance.Comment: LaTeX, 30 pages, 20 picture

    Photometric Redshift Requirements for Self-Calibration of Cluster Dark Energy Studies

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    The ability to constrain dark energy from the evolution of galaxy cluster counts is limited by the imperfect knowledge of cluster redshifts. Ongoing and upcoming surveys will mostly rely on redshifts estimated from broad-band photometry (photo-z's). For a Gaussian distribution for the cluster photo-z errors and a high cluster yield cosmology defined by the WMAP 1 year results, the photo-z bias and scatter needs to be known better than 0.003 and 0.03, respectively, in order not to degrade dark energy constrains by more than 10% for a survey with specifications similar to the South Pole Telescope. Smaller surveys and cosmologies with lower cluster yields produce weaker photo-z requirements, though relative to worse baseline constraints. Comparable photo-z requirements are necessary in order to employ self-calibration techniques when solving for dark energy and observable-mass parameters simultaneously. On the other hand, self-calibration in combination with external mass inferences helps reduce photo-z requirements and provides important consistency checks for future cluster surveys. In our fiducial model, training sets with spectroscopic redshifts for ~5%-15% of the detected clusters are required in order to keep degradations in the dark energy equation of state lower than 20%.Comment: 18 pages, 8 figures, submitted to PR

    The specific entropy of elliptical galaxies: an explanation for profile-shape distance indicators?

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    Dynamical systems in equilibrium have a stationary entropy; we suggest that elliptical galaxies, as stellar systems in a stage of quasi-equilibrium, may have a unique specific entropy. This uniqueness, a priori unknown, should be reflected in correlations between the parameters describing the mass (light) distribution in galaxies. Following recent photometrical work (Caon et al. 1993; Graham & Colless 1997; Prugniel & Simien 1997), we use the Sersic law to describe the light profile of elliptical galaxies and an analytical approximation to its three dimensional deprojection. The specific entropy is calculated supposing that the galaxy behaves as a spherical, isotropic, one-component system in hydrostatic equilibrium, obeying the ideal gas state equations. We predict a relation between the 3 parameters of the Sersic, defining a surface in the parameter space, an `Entropic Plane', by analogy with the well-known Fundamental Plane. We have analysed elliptical galaxies in Coma and ABCG 85 clusters and a group of galaxies (associated with NGC 4839). We show that the galaxies in clusters follow closely a relation predicted by the constant specific entropy hypothesis with a one-sigma dispersion of 9.5% around the mean value of the specific entropy. Assuming that the specific entropy is also the same for galaxies of different clusters, we are able to derive relative distances between the studied clusters. If the errors are only due to the determination of the specific entropy (about 10%), then the error in the relative distance determination should be less than 20% for rich clusters. We suggest that the unique specific entropy may provide a physical explanation for the distance indicators based on the Sersic profile put forward by Young & Currie (1994, 1995) and discussed by Binggeli & Jerjen (1998).Comment: Submitted to MNRAS (05/05/99), 15 pages, 10 figure
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