Mapping functions and critical behavior of percolation on rectangular domains

The existence probability $E_p$ and the percolation probability $P$ of the bond percolation on rectangular domains with different aspect ratios $R$ are studied via the mapping functions between systems with different aspect ratios. The superscaling behavior of $E_p$ and $P$ for such systems with exponents $a$ and $b$, respectively, found by Watanabe, Yukawa, Ito, and Hu in [Phys. Rev. Lett. \textbf{93}, 190601 (2004)] can be understood from the lower order approximation of the mapping functions $f_R$ and $g_R$ for $E_p$ and $P$, respectively; the exponents $a$ and $b$ can be obtained from numerically determined mapping functions $f_R$ and $g_R$, respectively.Comment: 17 pages with 6 figure

Geometry, thermodynamics, and finite-size corrections in the critical Potts model

We establish an intriguing connection between geometry and thermodynamics in the critical q-state Potts model on two-dimensional lattices, using the q-state bond-correlated percolation model (QBCPM) representation. We find that the number of clusters of the QBCPM has an energy-like singularity for q different from 1, which is reached and supported by exact results, numerical simulation, and scaling arguments. We also establish that the finite-size correction to the number of bonds, has no constant term and explains the divergence of related quantities as q --> 4, the multicritical point. Similar analyses are applicable to a variety of other systems.Comment: 12 pages, 6 figure

Universal scaling functions for bond percolation on planar random and square lattices with multiple percolating clusters

Percolation models with multiple percolating clusters have attracted much attention in recent years. Here we use Monte Carlo simulations to study bond percolation on $L_{1}\times L_{2}$ planar random lattices, duals of random lattices, and square lattices with free and periodic boundary conditions, in vertical and horizontal directions, respectively, and with various aspect ratio $L_{1}/L_{2}$. We calculate the probability for the appearance of $n$ percolating clusters, $W_{n},$ the percolating probabilities, $P$, the average fraction of lattice bonds (sites) in the percolating clusters, $_{n}$ ($_{n}$), and the probability distribution function for the fraction $c$ of lattice bonds (sites), in percolating clusters of subgraphs with $n$ percolating clusters, $f_{n}(c^{b})$ ($f_{n}(c^{s})$). Using a small number of nonuniversal metric factors, we find that $W_{n}$, $P$, $_{n}$ ($_{n}$), and $f_{n}(c^{b})$ ($f_{n}(c^{s})$) for random lattices, duals of random lattices, and square lattices have the same universal finite-size scaling functions. We also find that nonuniversal metric factors are independent of boundary conditions and aspect ratios.Comment: 15 pages, 11 figure

Exact Ampitude Ratio and Finite-Size Corrections for the M x N Square Lattice Ising Model The :

Let f, U and C represent, respectively, the free energy, the internal energy and the specific heat of the critical Ising model on the square M x N lattice with periodic boundary conditions. We find that N f and U are well-defined odd function of 1/N. We also find that ratios of subdominant (N^(-2 i - 1)) finite-size corrections amplitudes for the internal energy and the specific heat are constant. The free energy and the internal energy at the critical point are calculated asymtotically up to N^(-5) order, and the specific heat up to N^(-3) order.Comment: 18 pages, 4 figures, to be published in Phys. Rev. E 65, 1 February 200

Random-cluster multi-histogram sampling for the q-state Potts model

Using the random-cluster representation of the $q$-state Potts models we consider the pooling of data from cluster-update Monte Carlo simulations for different thermal couplings $K$ and number of states per spin $q$. Proper combination of histograms allows for the evaluation of thermal averages in a broad range of $K$ and $q$ values, including non-integer values of $q$. Due to restrictions in the sampling process proper normalization of the combined histogram data is non-trivial. We discuss the different possibilities and analyze their respective ranges of applicability.Comment: 12 pages, 9 figures, RevTeX

On second order elliptic equations with a small parameter

The Neumann problem with a small parameter $$(\dfrac{1}{\epsilon}L_0+L_1)u^\epsilon(x)=f(x) \text{for} x\in G, .\dfrac{\partial u^\epsilon}{\partial \gamma^\epsilon}(x)|_{\partial G}=0$$ is considered in this paper. The operators $L_0$ and $L_1$ are self-adjoint second order operators. We assume that $L_0$ has a non-negative characteristic form and $L_1$ is strictly elliptic. The reflection is with respect to inward co-normal unit vector $\gamma^\epsilon(x)$. The behavior of $\lim\limits_{\epsilon\downarrow 0}u^\epsilon(x)$ is effectively described via the solution of an ordinary differential equation on a tree. We calculate the differential operators inside the edges of this tree and the gluing condition at the root. Our approach is based on an analysis of the corresponding diffusion processes.Comment: 28 pages, 1 figure, revised versio

Josephson-vortex-flow terahertz emission in layered high-TcT_c superconducting single crystals

We report on the successful terahertz emission (0.6$\sim$1 THz) that is continuous and tunable in its frequency and power, by driving Josephson vortices in resonance with the collective standing Josephson plasma modes excited in stacked Bi$_2$Sr$_2$CaCu$_2$O$_{8+x}$ intrinsic Josephson junctions. Shapiro-step detection was employed to confirm the terahertz-wave emission. Our results provide a strong feasibility of developing long-sought solid-state terahertz-wave emission devices

HSV-2 Infection of Human Genital Epithelial Cells Upregulates TLR9 Expression Through the SP1/JNK Signaling Pathway

It is known that herpes simplex virus type 2 (HSV-2) triggers the activation of Toll-like receptor (TLR) 9 signaling pathway and the consequent production of antiviral cytokines in dendritic cells. However, the impact of HSV-2 infection on TLR9 expression and signaling in genital epithelial cells, the primary HSV-2 targets, has yet to be determined. In the current study, by using both human genital epithelial cell lines and primary genital epithelial cells as models, we found that HSV-2 infection enhances TLR9 expression at both mRNA and protein levels. Such enhancement is virus replication-dependent and CpG-independent, while the HSV-2-mediated upregulation of TLR9 does not activate TLR9 signaling pathway. Mechanistically, a SP1 binding site on TLR9 promoter appears to be essential for HSV-2-induced TLR9 transactivation. Upon HSV-2 infection, SP1 translocates from the cytoplasm to the nucleus, and consequently binds to TLR9 promoter. By using specific inhibitors, the JNK signaling pathway is shown to be involved in the HSV-2-induced TLR9 transactivation, while HSV-2 infection increases the phosphorylation but not the total level of JNK. In agreement, antagonism of JNK signaling pathway inhibits the HSV-2-induced SP1 nuclear translocation. Taken together, our study demonstrates that HSV-2 infection of human genital epithelial cells promotes TLR9 expression through SP1/JNK signaling pathway. Findings in this study provide insights into HSV-2-host interactions and potential targets for immune intervention