Related papers: Anisotropic Contact Process on Homogeneous Trees
The contact process on an infinite homogeneous tree is shown to exhibit at least two phase transitions as the infection parameter lambda is varied. For small values of lambda a single infection eventually dies out. For larger lambda the…
We study the supercritical contact process on Galton-Watson trees and periodic trees. We prove that if the contact process survives weakly then it dominates a supercritical Crump-Mode-Jagers branching process. Hence the number of infected…
This paper is concerned with contact process with random vertex weights on regular trees, and study the asymptotic behavior of the critical infection rate as the degree of the trees increasing to infinity. In this model, the infection…
It is known that the limiting behavior of the contact process strongly depends upon the geometry of the graph on which particles evolve: while the contact process on the regular lattice exhibits only two phases, the process on homogeneous…
The contact process is a simple model for the spread of an infection in a structured population. We consider a variant of this process on Bienaym\'e-Galton-Watson trees, where vertices are equipped with a random fitness representing…
We consider the contact process with infection rate $\lambda$ on $\mathbb{T}_n^d$, the $d$-ary tree of height $n$. We study the extinction time $\tau_{\mathbb{T}_n^d}$, that is, the random time it takes for the infection to disappear when…
We study the threshold $theta geq 2$ contact process on a homogeneous tree $T_b$ of degree $kappa = b + 1$, with infection parameter $lambda geq 0$ and started from a product measure with density $p$. The corresponding mean-field model…
We consider a contact process on $Z^d$ with two species that interact in a symbiotic manner. Each site can either be vacant or occupied by individuals of species $A$ and/or $B$. Multiple occupancy by the same species at a single site is…
Consider the following stochastic model for immune response. Each pathogen gives birth to a new pathogen at rate $\lambda$. When a new pathogen is born, it has the same type as its parent with probability $1 - r$. With probability $r$, a…
In this paper, we establish the necessary and sufficient criterion for the contact process on Galton-Watson trees (resp. random graphs) to exhibit the phase of extinction (resp. short survival). We prove that the survival threshold…
In this paper, we consider the threshold-one contact process and the threshold-one voter model w/o spontaneous death on homogeneous trees $\mathbb{T}_d$, $d\ge 2$. Mainly inspired by the corresponding arguments for ordinary contact…
A little over 25 years ago Pemantle pioneered the study of the contact process on trees, and showed that on homogeneous trees the critical values $\lambda_1$ and $\lambda_2$ for global and local survival were different. He also considered…
Recent progress in the study of the contact process [2] has verified that the extinction-survival threshold $\lambda_1$ on a Galton-Watson tree is strictly positive if and only if the offspring distribution $\xi$ has an exponential tail. In…
The key to our investigation is an improved (and in a sense sharp) understanding of the survival time of the contact process on star graphs. Using these results, we show that for the contact process on Galton-Watson trees, when the…
Motivated by recent findings of enhanced species survival when fragmented habitats are reconnected through narrow strips of land [S. Pimm, and C. N. Jenkins, Am. Sci. {\bf 107}(3), 162 (2019).], we study the effect of a corridor connecting…
Realistic modeling of ecological population dynamics requires spatially explicit descriptions that can take into account spatial heterogeneity as well as long-distance dispersal. Here, we present Monte Carlo simulations and numerical…
We consider the contact process with infection rate $\lambda$ on a random $(d+1)$-regular graph with $n$ vertices, $G_n$. We study the extinction time $\tau_{G_n}$ (that is, the random amount of time until the infection disappears) as $n$…
A little over 25 years ago Pemantle pioneered the study of the contact process on trees, and showed that the critical values $\lambda_1$ and $\lambda_2$ for global and local survival were different. Here, we will consider the case of trees…
We investigate a modified one-dimensional contact process with varying infection rates. Specifically, the infection spreads at rate $\lambda_e$ along the boundaries of the infected region and at rate $\lambda_i$ elsewhere. We establish the…
We study a two dimensional version of Neuhauser's long range sexual reproduction model and prove results that give bounds on the critical values $\lambda_f$ for the process to survive from a finite set and $\lambda_e$ for the existence of a…