Related papers: Competition in growth and urns
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 investigate the relationship between two kinds of vertex colorings of hypergraphs: unique-maximum colorings and conflict-free colorings. In a unique-maximum coloring, the colors are ordered, and in every hyperedge of the hypergraph the…
We model evolution of plants in a world, made up of different locations, with multiple environments (mutually exclusive and collectively exhaustive subsets of locations). Each environment (landmass) has temperature, rainfall, and other…
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…
Studying shape changing thick surfaces induced by differential growth helps us understand morphogenesis in biology and offers opportunities for device design. While ideal 2D differential growth maps have been well studied for both isotropic…
Bootstrap percolation is an often used model to study the spread of diseases, rumors, and information on sparse random graphs. The percolation process demonstrates a critical value such that the graph is either almost completely affected or…
The evolution of states of a spatial ecological model is studied. The model describes an infinite population of point entities placed in $\mathbb{R}^d$ which reproduce themselves at distant points (disperse) and die with rate that includes…
An urn contains balls of d colors. At each time, a ball is drawn and then replaced together with a random number of balls of the same color. Assuming that some colors are dominated by others, we prove central limit theorems. Some…
Competition is one of the most fundamental phenomena in physics, biology and economics. Recent studies of the competition between innovations have highlighted the influence of switching costs and interaction networks, but the problem is…
We discuss a cellular automata model to study the competition between an emergent better fitted species against an existing majority species. The model implement local fights among small group of individual and a synchronous random walk on…
The two-type Richardson model describes the growth of two competing infections on $\mathbb{Z}^d$. At time 0 two disjoint finite sets $\xi_1,\xi_2\subset \mathbb{Z}^d$ are infected with type 1 and type 2 infection respectively. An uninfected…
We study competition of two spreading colors starting from single sources on the configuration model with i.i.d. degrees following a power-law distribution with exponent tau in (2,3). In this model two colors spread with a fixed but not…
We consider, as proposed and studied in Hofstad et.\ al.\ \cite{HHKR}, a class of graph-based "interacting urn"-type Polya urn model inspired by neuronal processing in the brain where a signal enters the brain at some (randomly) chosen…
The behaviour and functioning of a variety of complex physical and biological systems depend on the spatial organisation of their constituent units, and on the presence and formation of clusters of functionally similar or related…
P{\'o}lya urns are urns where at each unit of time a ball is drawn and is replaced with some other balls according to its colour. We introduce a more general model: The replacement rule depends on the colour of the drawn ball and the value…
A stochastic birth-death competition model for particles with excluded volume is proposed. The particles move, reproduce, and die on a regular lattice. While the death rate is constant, the birth rate is spatially nonlocal and implements…
In majority bootstrap percolation on a graph G, an infection spreads according to the following deterministic rule: if at least half of the neighbours of a vertex v are already infected, then v is also infected, and infected vertices remain…
We consider a population organised hierarchically with respect to size in such a way that the growth rate of each individual depends only on the presence of larger individuals. As a concrete example one might think of a forest, in which the…
We introduce two novel evolutionary formulations of the problem of coloring the nodes of a graph. The first formulation is based on the relationship that exists between a graph's chromatic number and its acyclic orientations. It views such…
We study a geometrically constrained coalescence model derived from spin systems. Given two probability distributions $\mathbb{P}_R$ and $\mathbb{P}_B$ on the positive reals with finite means, colour the real line alternately with red and…