Related papers: First-passage competition with different speeds: p…
For a finite set of integers such that the first few gaps between its consecutive elements equal $a$, while the remaining gaps equal $b$, we study dense packings of its translates on the line. We obtain an explicit lower bound on the…
: From the epoch of recombination $(z\approx 10^3)$ till today, the typical density contrasts have grown by a factor of about $10^6$ in a Friedmann universe with $\Omega=1$. However, during the same epoch the typical gravitational potential…
For a two-species reaction-diffusion-competition system on a domain that translates at constant speed and/or whose boundary varies periodically with time, we prove sufficient conditions such that one species can, and cannot, invade an…
We study a pinned variant of Bourgain's theorem, concerning the occurrence of affine copies of $k$-point patterns in $\mathbb{R}^d$. Focusing on the case $k=2$, which corresponds to pinned distances, we show that the classical conclusion…
Epidemic spreading often occurs in spatially heterogeneous environments, yet how quenched heterogeneity reshapes its onset and critical dynamics remains poorly understood. The diffusive epidemic process, a minimal reaction-diffusion model…
In evolutionary game theory, an important measure of a mutant trait (strategy) is its ability to invade and take over an otherwise-monomorphic population. Typically, one quantifies the success of a mutant strategy via the probability that a…
Making use of a Rice-like series expansion, for a class of stationary Gaussian processes the asymptotic behavior of the first passage time probability density function through certain time-varying boundaries, including periodic boundaries,…
We study the factorised steady state of a general class of mass transport models in which mass, a conserved quantity, is transferred stochastically between sites. Condensation in such models is exhibited when above a critical mass density…
We study the large scale behaviour of a population consisting of two types which evolve in dimension d = 1, 2 according to a spatial Lambda- Fleming-Viot process subject to random time-independent selection. If one of the two types is rare…
In Part 1, we introduced a stochastic model of an infectious disease, based on the BDI (birth and death with immigration) process. We showed that random processes defined by this model can capture the essence of the stochastic, often…
We consider a stochastic individual-based model of adaptive dynamics for an asexually reproducing population with mutation, with linear birth and death rates, as well as a density-dependent competition. To depict repeating changes of the…
In $1993$, Holt and Lawton introduced a stochastic model of two host species parasitized by a common parasitoid species. We introduce and analyze a generalization of these stochastic difference equations with any number of host species,…
The complex interplay between population movements in space and non-homogeneous mixing patterns have so far hindered the fundamental understanding of the conditions for spatial invasion through a general theoretical framework. To address…
In this paper, we study a finite population undergoing discrete, nonoverlapping generations, that is structured into $D$ demes, each containing $N$ individuals of two possible types, $A$ and $B$, whose viability coefficients, $s_A$ and…
We provide a new existence result for weak solutions to the one-dimensional Euler equations with a maximal density constraint, corresponding to a unilateral constraint on the density. Such models arise in the description of congestion…
Convex combinations of i.i.d. random variables without a finite mean can behave in a strikingly different way from the finite-mean case: as the weight vector becomes more balanced, the resulting combination may become stochastically larger,…
We study a discrete time spatial branching system on $\mathbb{Z}^d$ with logistic-type local regulation at each deme depending on a weighted average of the population in neighboring demes. We show that the system survives for all time with…
We introduce a spatial stochastic process on the lattice Z^d to model mass extinctions. Each site of the lattice may host a flock of up to N individuals. Each individual may give birth to a new individual at the same site at rate \phi until…
It has long been known that antibiotic treatment will not completely kill off a bacteria population. For many species a small fraction of bacteria is not sensitive to antibiotics. These bacteria are said to persist. Recently it has been…
This paper is concerned with the limit, as the interspecific competition rate goes to infinity, of pulsating front solutions in space-periodic media for a bistable two-species competition--diffusion Lotka--Volterra system. We distinguish…