Related papers: Competition between growths governed by Bernoulli …
Eulerian percolation on Z 2 with parameter p is the classical Bernoulli bond percolation with parameter p conditioned on the fact that every site has an even degree. We first explain why Eulerian percolation with parameter p coincides with…
We study the dynamics of upper and lower bounds of squared concurrence.Our results are similar to that of Konard et al. and can help the estimation of high-dimension bipartite entanglement in experiments.
We study a new geometric bootstrap percolation model, line percolation, on the $d$-dimensional integer grid $[n]^d$. In line percolation with infection parameter $r$, infection spreads from a subset $A\subset [n]^d$ of initially infected…
Concurrence is an important entanglement measure for states in finite-dimensional quantum systems that was explored intensively in the last decade. In this paper, we extend the concept of concurrence to infinite-dimensional bipartite…
We find evidence for a continuum limit of a particular causal set dynamics which depends on only a single ``coupling constant'' $p$ and is easy to simulate on a computer. The model in question is a stochastic process that can also be…
The dynamics of the spread of contagions such as viruses, infectious diseases or even rumors/opinions over contact networks (graphs) have effectively been captured by the well known \textit{Susceptible-Infected-Susceptible} ($SIS$) epidemic…
Survival and percolation probabilities are most important quantities in the theory and in the application of growth models with spreading. We construct field theoretical expressions for these probabilities which are feasible for…
We consider a variation of the Hastings-Levitov model HL(0) for random growth in which the growing cluster consists of two competing regions. We allow the size of successive particles to depend both on the region in which the particle is…
We study the competition interface between two growing clusters in a growth model associated to last-passage percolation. When the initial unoccupied set is approximately a cone, we show that this interface has an asymptotic direction with…
We investigate a model of epidemic spreading with partial immunization which is controlled by two probabilities, namely, for first infections, $p_0$, and reinfections, $p$. When the two probabilities are equal, the model reduces to directed…
When competing species grow into new territory, the population is dominated by descendants of successful ancestors at the expansion front. Successful ancestry depends on both the reproductive advantage (fitness), as well as ability and…
We consider a nonlinear Dirichlet problem driven by the $(p,q)$-Laplacian with $1<q<p$. The reaction is parametric and exhibits the competing effects of a singular term and of concave and convex nonlinearities. We are looking for positive…
To understand the biodiversity of an ecosystem cannot be understood by solely analyzing the pair relations of competing species. Instead, we should consider multi-point interactions because the presence of a third party could change the…
Let $\mathbb{G}=\left(\mathbb{V},\mathbb{E}\right)$ be the graph obtained by taking the cartesian product of an infinite and connected graph $G=(V,E)$ and the set of integers $\mathbb{Z}$. We choose a collection $\mathcal{C}$ of finite…
We study the macroscopic geometry of first-passage competition on the integer lattice $Z^d$, with a particular interest in describing the behavior when one species initially occupies the exterior of a cone. First-passage competition is a…
This is the first of two papers where we discuss the limits imposed by competition to the biodiversity of species communities. In this first paper we study the coexistence of competing species at the fixed point of population dynamic…
A Markov evolution of a system of point particles in $\mathbb{R}^d$ is described at micro-and mesoscopic levels. The particles reproduce themselves at distant points (dispersal) and die, independently and under the influence of each other…
We consider bootstrap percolation on the binomial random graph $G(n,p)$ with infection threshold $r\in \mathbb{N}$, an infection process which starts from a set of initially infected vertices and in each step every vertex with at least $r$…
It is known that the competitive exclusion principle holds for a large kind of models involving several species competing for a single resource in an homogeneous environment. Various works indicate that the coexistence is possible in an…
We study a competition-diffusion model while performing simultaneous homogenization and strong competition limits. The limit problem is shown to be a Stefan type evolution equation with effective coefficients. We also perform some numerical…