相关论文: Competition between growths governed by Bernoulli …
A competition model on $\N^{2}$ between three clusters and governed by directed last passage percolation is considered. We prove that coexistence, i.e. the three clusters are simultaneously unbounded, occurs with probability $6-8\log2$.…
We study two competing growth models. Each of these models describes the spread of a finite number of infections on a graph. Each infection evolves like an (oriented or unoriented) first passage percolation process except that once a vertex…
Assuming repeated independent sampling from a Bernoulli distribution with two possible outcomes S and F, there are formulas for computing the probability of one specific pattern of consecutive outcomes (such as SSFFSS) winning (i.e. being…
A competition model on $\mathbb{Z}_+^{2}$ governed by directed last passage percolation is considered. A stochastic domination argument between subtrees of the last passage percolation is put forward.
The parameterized entanglement monotone, the $q$-concurrence, is also a reasonable parameterized entanglement measure. By exploring the properties of the $q$-concurrence with respect to the positive partial transposition and realignment of…
We consider the following oriented percolation model of $\mathbb {N} \times \mathbb{Z}^d$: we equip $\mathbb {N}\times \mathbb{Z}^d$ with the edge set $\{[(n,x),(n+1,y)] | n\in \mathbb {N}, x,y\in \mathbb{Z}^d\}$, and we say that each edge…
A stochastic model, describing the growth of two competing infections on $\mathbb{R}^d$, is introduced. The growth is driven by outbursts in the infected region, an outburst in the type 1 (2) infected region transmitting the type 1 (2)…
Diseases emerge, persist and vanish in an ongoing battle for available hosts. Hosts, on the other hand, defend themselves by developing immunity that limits the ability of pathogens to reinfect them. We here explore a multi-disease system…
In growing populations, the fate of mutations depends on their competitive ability against the ancestor and their ability to colonize new territory. Here we present a theory that integrates both aspects of mutant fitness by coupling the…
The competitive exclusion principle in epidemiology implies that when competing strains of a pathogen provide complete protection for each other, the strain with the largest reproduction number outcompetes the other strains and drives them…
In this note, we investigate Bernoulli oriented bond percolation with parameter $p$ on $\mathbb{Z}^2$. In addition to the standard edges, which are open with probability $p$, we introduce diagonal edges each open with probability…
A model named `Colored Percolation' has been introduced with its infinite number of versions in two dimensions. The sites of a regular lattice are randomly occupied with probability $p$ and are then colored by one of the $n$ distinct colors…
We consider Bernoulli first-passage percolation on the $d$-dimensional hypercubic lattice with $d \geq 2$. The passage time of edge $e$ is $0$ with probability $p$ and $1$ with probability $1-p$, independently of each other. Let $p_c$ be…
The possible control of competitive invasion by infection of the invader and multiplicative noise is studied. The basic model is the Lotka-Volterra competition system with emergent carrying capacities. Several stationary solutions of the…
On a locally finite, infinite tree $T$, let $p_c(T)$ denote the critical probability for Bernoulli percolation. We prove that every positively associated, finite-range dependent percolation model on $T$ with marginals $p > p_c(T)$ must…
We introduce a two-type first passage percolation competition model on infinite connected graphs as follows. Type 1 spreads through the edges of the graph at rate 1 from a single distinguished site, while all other sites are initially…
Resource-based competition between microorganisms species in continuous culture has been studied extensively both experimentally and theoretically, mostly for bacteria through Monod and and Contois "constant yield" models, or for…
We study the size of the near-critical window for Bernoulli percolation on $\mathbb Z^d$. More precisely, we use a quantitative Grimmett-Marstrand theorem to prove that the correlation length, both below and above criticality, is bounded…
We define the $Q$-factor in the percolation problem as the quotient of the size of the largest cluster and the average size of all clusters. As the occupation probability $p$ is increased, the $Q$-factor for the system size $L$ grows…
We study a spatially homogeneous model of a market where several agents or companies compete for a wealth resource. In analogy with ecological systems the simplest case of such models shows a kind of "competitive exclusion" principle.…