Related papers: The critical contact process in a randomly evolvin…
This paper gives a new, simple proof of the known fact that for contact processes on general lattices, in the subcritical regime the expected number of infected sites decays exponentially fast as time tends to infinity. The proof also…
We propose the following model for speciation and extinction. Birth and deaths occur according to spatially inhomogeneous contact rates. We assume that the ratio of the birth rate over the death rate at a site converges to some limit as the…
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 consider the extinction time of the contact process on increasing sequences of finite graphs obtained from a variety of random graph models. Under the assumption that the infection rate is above the critical value for the process on the…
A subcritical branching process in random environment (BPRE) is considered whose associated random walk does not satisfy the Cramer condition. The asymptotics for the survival probability of the process is investigated, and a Yaglom type…
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…
In this article, we introduce a contact process with aging: in this generalization of the classical contact process, each particle has an integer age that influences its ability to give birth. We prove here a shape theorem for this process…
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 $n$…
Motivated by a model of an area-wide integrated pest management, we develop an interacting particle system evolving in a random environment. It is a generalised contact process in which the birth rate takes two possible values, determined…
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 give a construction of a tree in which the contact process with any positive infection rate survives but, if a certain privileged edge $e^*$ is removed, one obtains two subtrees in which the contact process with infection rate smaller…
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…
The long-time dynamics of the critical contact process which is brought suddenly out of an uncorrelated initial state undergoes ageing in close analogy with quenched magnetic systems. In particular, we show through Monte Carlo simulations…
The contact process is a non-equilibrium Hamiltonian model that, even in one dimension, lacks an exact solution and has been extensively studied via Monte Carlo simulations, both in steady-state and time-dependent scenarios. Although the…
In this work we study the one-dimensional contact process with diffusion using two different approaches to research the critical properties of this model: the supercritical series expansions and finite-size exact solutions. With special…
We study a two-level contact process. We think of fleas living on a species of animals. The animals are a supercritical contact process in $\mathbb{Z}^d$. The contact process acts as the random environment for the fleas. The fleas do not…
We show that the contact process on a random $d$-regular graph initiated by a single infected vertex obeys the "cutoff phenomenon" in its supercritical phase. In particular, we prove that when the infection rate is larger than the critical…
In this paper, we derive a precise estimate for the mean extinction time of the contact process with a fixed infection rate on a star graph with $N$ leaves. Specifically, we determine not only the exponential main factor but also the exact…
The regular tree corresponds to the random regular graph as its local limit. For this reason the famous double phase transition of the contact process on regular tree has been seen to correspond to a phase transition on the large random…
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…