70 research outputs found

    On two fragmentation schemes with algebraic splitting probability

    Full text link

    Random walks pertaining to a class of deterministic weighted graphs

    Full text link
    In this note, we try to analyze and clarify the intriguing interplay between some counting problems related to specific thermalized weighted graphs and random walks consistent with such graphs

    Nonextensivity and multifractality in low-dimensional dissipative systems

    Full text link
    Power-law sensitivity to initial conditions at the edge of chaos provides a natural relation between the scaling properties of the dynamics attractor and its degree of nonextensivity as prescribed in the generalized statistics recently introduced by one of us (C.T.) and characterized by the entropic index qq. We show that general scaling arguments imply that 1/(1−q)=1/αmin−1/αmax1/(1-q) = 1/\alpha_{min}-1/\alpha_{max}, where αmin\alpha_{min} and αmax\alpha_{max} are the extremes of the multifractal singularity spectrum f(α)f(\alpha) of the attractor. This relation is numerically checked to hold in standard one-dimensional dissipative maps. The above result sheds light on a long-standing puzzle concerning the relation between the entropic index qq and the underlying microscopic dynamics.Comment: 12 pages, TeX, 4 ps figure

    Anomalous diffusion associated with nonlinear fractional derivative Fokker-Planck-like equation: Exact time-dependent solutions

    Full text link
    We consider the d=1d=1 nonlinear Fokker-Planck-like equation with fractional derivatives ∂∂tP(x,t)=D∂γ∂xÎł[P(x,t)]Îœ\frac{\partial}{\partial t}P(x,t)=D \frac{\partial^{\gamma}}{\partial x^{\gamma}}[P(x,t) ]^{\nu}. Exact time-dependent solutions are found for Îœ=2−γ1+Îł \nu = \frac{2-\gamma}{1+ \gamma} (−∞<γ≀2-\infty<\gamma \leq 2). By considering the long-distance {\it asymptotic} behavior of these solutions, a connection is established, namely q=Îł+3Îł+1q=\frac{\gamma+3}{\gamma+1} (0<γ≀20<\gamma \le 2), with the solutions optimizing the nonextensive entropy characterized by index qq . Interestingly enough, this relation coincides with the one already known for L\'evy-like superdiffusion (i.e., Îœ=1\nu=1 and 0<γ≀20<\gamma \le 2). Finally, for (Îł,Îœ)=(2,0)(\gamma,\nu)=(2, 0) we obtain q=5/3q=5/3 which differs from the value q=2q=2 corresponding to the Îł=2\gamma=2 solutions available in the literature (Îœ<1\nu<1 porous medium equation), thus exhibiting nonuniform convergence.Comment: 3 figure

    Exact Scale Invariance in Mixing of Binary Candidates in Voting Model

    Full text link
    We introduce a voting model and discuss the scale invariance in the mixing of candidates. The Candidates are classified into two categories Ό∈{0,1}\mu\in \{0,1\} and are called as `binary' candidates. There are in total N=N0+N1N=N_{0}+N_{1} candidates, and voters vote for them one by one. The probability that a candidate gets a vote is proportional to the number of votes. The initial number of votes (`seed') of a candidate ÎŒ\mu is set to be sÎŒs_{\mu}. After infinite counts of voting, the probability function of the share of votes of the candidate ÎŒ\mu obeys gamma distributions with the shape exponent sÎŒs_{\mu} in the thermodynamic limit Z0=N1s1+N0s0→∞Z_{0}=N_{1}s_{1}+N_{0}s_{0}\to \infty. Between the cumulative functions {xÎŒ}\{x_{\mu}\} of binary candidates, the power-law relation 1−x1∌(1−x0)α1-x_{1} \sim (1-x_{0})^{\alpha} with the critical exponent α=s1/s0\alpha=s_{1}/s_{0} holds in the region 1−x0,1−x1<<11-x_{0},1-x_{1}<<1. In the double scaling limit (s1,s0)→(0,0)(s_{1},s_{0})\to (0,0) and Z0→∞Z_{0} \to \infty with s1/s0=αs_{1}/s_{0}=\alpha fixed, the relation 1−x1=(1−x0)α1-x_{1}=(1-x_{0})^{\alpha} holds exactly over the entire range 0≀x0,x1≀10\le x_{0},x_{1} \le 1. We study the data on horse races obtained from the Japan Racing Association for the period 1986 to 2006 and confirm scale invariance.Comment: 19 pages, 8 figures, 2 table

    A Pearson-Dirichlet random walk

    Full text link
    A constrained diffusive random walk of n steps and a random flight in Rd, which can be expressed in the same terms, were investigated independently in recent papers. The n steps of the walk are identically and independently distributed random vectors of exponential length and uniform orientation. Conditioned on the sum of their lengths being equal to a given value l, closed-form expressions for the distribution of the endpoint of the walk were obtained altogether for any n for d=1, 2, 4 . Uniform distributions of the endpoint inside a ball of radius l were evidenced for a walk of three steps in 2D and of two steps in 4D. The previous walk is generalized by considering step lengths which are distributed over the unit (n-1) simplex according to a Dirichlet distribution whose parameters are all equal to q, a given positive value. The walk and the flight above correspond to q=1. For any d >= 3, there exist, for integer and half-integer values of q, two families of Pearson-Dirichlet walks which share a common property. For any n, the d components of the endpoint are jointly distributed as are the d components of a vector uniformly distributed over the surface of a hypersphere of radius l in a space Rk whose dimension k is an affine function of n for a given d. Five additional walks, with a uniform distribution of the endpoint in the inside of a ball, are found from known finite integrals of products of powers and Bessel functions of the first kind. They include four different walks in R3 and two walks in R4. Pearson-Liouville random walks, obtained by distributing the total lengths of the previous Pearson-Dirichlet walks, are finally discussed.Comment: 33 pages 1 figure, the paper includes the content of a recently submitted work together with additional results and an extended section on Pearson-Liouville random walk

    The pregnane X receptor drives sexually dimorphic hepatic changes in lipid and xenobiotic metabolism in response to gut microbiota in mice.

    Get PDF
    The gut microbiota-intestine-liver relationship is emerging as an important factor in multiple hepatic pathologies, but the hepatic sensors and effectors of microbial signals are not well defined. By comparing publicly available liver transcriptomics data from conventional vs. germ-free mice, we identified pregnane X receptor (PXR, NR1I2) transcriptional activity as strongly affected by the absence of gut microbes. Microbiota depletion using antibiotics in Pxr &lt;sup&gt;+/+&lt;/sup&gt; vs Pxr &lt;sup&gt;-/-&lt;/sup&gt; C57BL/6J littermate mice followed by hepatic transcriptomics revealed that most microbiota-sensitive genes were PXR-dependent in the liver in males, but not in females. Pathway enrichment analysis suggested that microbiota-PXR interaction controlled fatty acid and xenobiotic metabolism. We confirmed that antibiotic treatment reduced liver triglyceride content and hampered xenobiotic metabolism in the liver from Pxr &lt;sup&gt;+/+&lt;/sup&gt; but not Pxr &lt;sup&gt;-/-&lt;/sup&gt; male mice. These findings identify PXR as a hepatic effector of microbiota-derived signals that regulate the host's sexually dimorphic lipid and xenobiotic metabolisms in the liver. Thus, our results reveal a potential new mechanism for unexpected drug-drug or food-drug interactions. Video abstract
    • 

    corecore