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Maria Deijfen

Publications and source records attributed to Maria Deijfen.

At least 19 recordsLinked to original sources

Surviving from the tip of a cone in competing first-passage percolation

In two-type first passage percolation on $\mathbb{Z}^2$, two entities compete to capture the sites of the lattice. The entities spread between nearest neighbor sites at times specified by random passage times associated with the edges. We consider the case when both types have the same passage time distribution, with one type starting at the origin and the other from an infinite cone with tip at the origin and pointing in direction $\theta$. Itai Benjamini has suggested that the type starting at the origin can grow unboundedly if and only if the slope of the cone is strictly smaller than $\pi/2$, so that the cone does not fill a whole half-plane. The main result is that this is correct for any $\theta$ such that the asymptotic shape of the one-type process has a tangent line with direction $\theta$. The proofs are based on a description of infinite time-minimizing paths in terms of Busemann functions together with local modification arguments.

math.PR

Gaussian fluctuations in mean field stable matchings

Two sets of objects of size $n$ are to be matched to each other based on i.i.d. costs associated to every pair of objects. Objects prefer to be matched as cheaply as possible, and a matching is said to be stable if there is no pair of objects that would prefer to match to each other rather than to their current partners. Properties of such matchings are analysed for cost distributions with a density $\rho$ satisfying $\rho(x)/(dx^{d-1})\to 1$ as $x\to 0^+$, where the number $d$ is known as the pseudo-dimension. For $d>0$, the typical matching cost is shown to be of order $n^{-1/d}$, with an explicit distributional limit. For $d>1$ the total matching cost is shown to be of order $n^{1-1/d}$, and to obey a law of large numbers. For $d>2$ the fluctuations of the total matching cost are shown to be of order $n^{1/2-1/d}$, and to obey a central limit theorem.

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Mean field stable matchings

Consider the complete bipartite graph on $n+n$ vertices where the edges are equipped with i.i.d. exponential costs. A matching of the vertices is stable if it does not contain any pair of vertices where the connecting edge is cheaper than both matching costs. There exists a unique stable matching obtained by iteratively pairing vertices with small edge costs. We show that the total cost $C_{n,n}$ of this matching is of order $\log n$ with bounded variance, and that $C_{n,n}-\log n$ converges to a Gumbel distribution. We also show that the typical cost of an edge in the matching is of order $1/n$, with an explicit density on this scale, and analyze the rank of a typical edge. These results parallel those of Aldous for the minimal cost matching in the same setting. We then consider the sensitivity of the matching and the matching cost to perturbations of the underlying edge costs. The matching itself is shown to be robust in the sense that two matchings based on largely identical edge costs will have a substantial overlap. The matching cost however is shown to be noise sensitive, as a result of the fact that the most expensive edges will with high probability be replaced after resampling. Our proofs also apply to the complete (unipartite) graph and the results in this case are qualitatively similar.

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Geometric random intersection graphs with general connection probabilities

Let $\mathcal{V}$ and $\mathcal{U}$ be the point sets of two independent homogeneous Poisson processes on $\mathbb{R}^d$. A graph $\mathcal{G}_\mathcal{V}$ with vertex set $\mathcal{V}$ is constructed by first connecting pairs of points $(v,u)$ with $v\in\mathcal{V}$ and $u\in\mathcal{U}$ independently with probability $g(v-u)$, where $g$ is a non-increasing radial function, and then connecting two points $v_1,v_2\in\mathcal{V}$ if and only if they have a joint neighbor $u\in\mathcal{U}$. This gives rise to a random intersection graph on $\mathbb{R}^d$. Local properties of the graph, including the degree distribution, are investigated and quantified in terms of the intensities of the underlying Poisson processes and the function $g$. Furthermore, the percolation properties of the graph are characterized and shown to differ depending on whether $g$ has bounded or unbounded support.

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Chaos, concentration and multiple valleys in first-passage percolation

A decade and a half ago Chatterjee established the first rigorous connection between anomalous fluctuations and a chaotic behaviour of the ground state in certain Gaussian disordered systems. The purpose of this paper is to show that Chatterjee's work gives evidence of a more general principle, by establishing an analogous connection between fluctuations and chaos in the context of first-passage percolation. The notion of `chaos' here refers to the sensitivity of the time-minimising path between two points when exposed to a slight perturbation. More precisely, we resample a small proportion of the edge weights, and find that a vanishing fraction of the edges on the time-minimising path still belongs to the time-minimising path obtained after resampling. We also identify the point at which the system transitions from being stable to being chaotic in terms of the variance of the system. Finally we show that the chaotic behaviour implies the existence of a large number of almost-optimal paths that are almost disjoint from the time-minimising path, a phenomenon known as 'multiple valleys'.

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From stability to chaos in last-passage percolation

We study the transition from stability to chaos in a dynamic last passage percolation model on $\mathbb{Z}^d$ with random weights at the vertices. Given an initial weight configuration at time $0$, we perturb the model over time in such a way that the weight configuration at time $t$ is obtained by resampling each weight independently with probability $t$. On the cube $[0,n]^d$, we study geodesics, that is, weight-maximizing up-right paths from $(0,0, \dots, 0)$ to $(n,n, \dots, n)$, and their passage time $T$. Under mild conditions on the weight distribution, we prove a phase transition between stability and chaos at $t \asymp \frac{1}{n}\mathrm{Var}(T)$. Indeed, as $n$ grows large, for small values of $t$, the passage times at time $0$ and time $t$ are highly correlated, while for large values of $t$, the geodesics become almost disjoint.

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The winner takes it all but one

We study competing first passage percolation on graphs generated by the configuration model with infinite-mean degrees. Initially, two uniformly chosen vertices are infected with type 1 and type 2 infection, respectively, and the infection then spreads via nearest neighbors in the graph. The time it takes for the type 1 (resp. 2) infection to traverse an edge $e$ is given by a random variable $X_1(e)$ (resp. $X_2(e)$) and, if the vertex at the other end of the edge is still uninfected, it then becomes type 1 (resp. 2) infected and immune to the other type. Assuming that the degrees follow a power-law distribution with exponent $\tau \in (1,2)$, we show that, with high probability as the number of vertices tends to infinity, one of the infection types occupies all vertices except for the starting point of the other type. Moreover, both infections have a positive probability of winning regardless of the passage times distribution. The result is also shown to hold for the erased configuration model, where self-loops are erased and multiple edges are merged, and when the degrees are conditioned to be smaller than $n^\alpha$ for some $\alpha > 0$.

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Competition on $\mathbb{Z}^d$ driven by branching random walk

A competition process on $\mathbb{Z}^d$ is considered, where two species compete to color the sites. The entities are driven by branching random walks. Specifically red (blue) particles reproduce in discrete time and place offspring according to a given reproduction law, which may be different for the two types. When a red (blue) particle is placed at a site that has not been occupied by any particle before, the site is colored red (blue) and keeps this color forever. The types interact in that, when a particle is placed at a site of opposite color, the particle adopts the color of the site with probability $p\in[0,1]$. Can a given type color infinitely many sites? Can both types color infinitely many sites simultaneously? Partial answers are given to these questions and many open problems are formulated.

math.PR

A preferential attachment model with random initial degrees

In this paper, a random graph process ${G(t)}_{t\geq 1}$ is studied and its degree sequence is analyzed. Let $(W_t)_{t\geq 1}$ be an i.i.d. sequence. The graph process is defined so that, at each integer time $t$, a new vertex, with $W_t$ edges attached to it, is added to the graph. The new edges added at time t are then preferentially connected to older vertices, i.e., conditionally on $G(t-1)$, the probability that a given edge is connected to vertex i is proportional to $d_i(t-1)+δ$, where $d_i(t-1)$ is the degree of vertex $i$ at time $t-1$, independently of the other edges. The main result is that the asymptotical degree sequence for this process is a power law with exponent $τ=\min\{τ_{W}, τ_{P}\}$, where $τ_{W}$ is the power-law exponent of the initial degrees $(W_t)_{t\geq 1}$ and $τ_{P}$ the exponent predicted by pure preferential attachment. This result extends previous work by Cooper and Frieze, which is surveyed.

math.PR

The initial set in the frog model is irrelevant

In this note, we consider the frog model on $\mathbb{Z}^d$ and a two-type version of it with two types of particles. For the one-type model, we show that the asymptotic shape does not depend on the initially activated set and the configuration there. For the two-type model, we show that the possibility for the types to coexist in that both of them activate infinitely many particles does not depend on the choice of the initially activated sets and the configurations there.

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The Schelling model on $\mathbb{Z}$

A version of the Schelling model on $\mathbb{Z}$ is defined, where two types of agents are allocated on the sites. An agent prefers to be surrounded by other agents of its own type, and may choose to move if this is not the case. It then sends a request to an agent of opposite type chosen according to some given moving distribution and, if the move is beneficial for both agents, they swap location. We show that certain choices in the dynamics are crucial for the properties of the model. In particular, the model exhibits different asymptotic behavior depending on whether the moving distribution has bounded or unbounded support. Furthermore, the behavior changes if the agents are lazy in the sense that they only swap location if this strictly improves their situation. Generalizations to a version that includes multiple types are discussed. The work provides a rigorous analysis of so called Kawasaki dynamics on an infinite structure with local interactions.

math.PR

Competing frogs on $\mathbb{Z}^d$

A two-type version of the frog model on $\mathbb{Z}^d$ is formulated, where active type $i$ particles move according to lazy random walks with probability $p_i$ of jumping in each time step ($i=1,2$). Each site is independently assigned a random number of particles. At time 0, the particles at the origin are activated and assigned type 1 and the particles at one other site are activated and assigned type 2, while all other particles are sleeping. When an active type $i$ particle moves to a new site, any sleeping particles there are activated and assigned type $i$, with an arbitrary tie-breaker deciding the type if the site is hit by particles of both types in the same time step. We show that the event $G_i$ that type $i$ activates infinitely many particles has positive probability for all $p_1,p_2\in(0,1]$ ($i=1,2$). Furthermore, if $p_1=p_2$, then the types can coexist in the sense that $\mathbb{P}(G_1\cap G_2)>0$. We also formulate several open problems. For instance, we conjecture that, when the initial number of particles per site has a heavy tail, the types can coexist also when $p_1\neq p_2$.

math.PR

The two-type Richardson model in the half-plane

The two-type Richardson model describes the growth of two competing infection types on the two or higher dimensional integer lattice. For types that spread with the same intensity, it is known that there is a positive probability for infinite coexistence, while for types with different intensities, it is conjectured that infinite coexistence is not possible. In this paper we study the two-type Richardson model in the upper half-plane $\mathbb{Z}\times\mathbb{Z}_+$, and prove that coexistence of two types starting on the horizontal axis has positive probability if and only if the types have the same intensity.

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The tail does not determine the size of the giant

The size of the giant component in the configuration model, measured by the asymptotic fraction of vertices in the component, is given by a well-known expression involving the generating function of the degree distribution. In this note, we argue that the distribution over small degrees is more important for the size of the giant component than the precise distribution over very large degrees. In particular, the tail behavior of the degree distribution does not play the same crucial role for the size of the giant as it does for many other properties of the graph. Upper and lower bounds for the component size are derived for an arbitrary given distribution over small degrees $d\leq L$ and given expected degree, and numerical implementations show that these bounds are close already for small values of $L$. On the other hand, examples illustrate that, for a fixed degree tail, the component size can vary substantially depending on the distribution over small degrees.

math.PR

Competing first passage percolation on random graphs with finite variance degrees

We study the growth of two competing infection types on graphs generated by the configuration model with a given degree sequence. Starting from two vertices chosen uniformly at random, the infection types spread via the edges in the graph in that an uninfected vertex becomes type 1 (2) infected at rate $λ_1$ ($λ_2$) times the number of nearest neighbors of type 1 (2). Assuming (essentially) that the degree of a randomly chosen vertex has finite second moment, we show that if $λ_1=λ_2$, then the fraction of vertices that are ultimately infected by type 1 converges to a continuous random variable $V\in(0,1)$, as the number of vertices tends to infinity. Both infection types hence occupy a positive (random) fraction of the vertices. If $λ_1\neq λ_2$, on the other hand, then the type with the larger intensity occupies all but a vanishing fraction of the vertices. Our results apply also to a uniformly chosen simple graph with the given degree sequence.

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Birds of a feather or opposites attract - effects in network modelling

We study properties of some standard network models when the population is split into two types and the connection pattern between the types is varied. The studied models are generalizations of the Erdős-Rényi graph, the configuration model and a preferential attachment graph. For the Erdős-Rényi graph and the configuration model, the focus is on the component structure. We derive expressions for the critical parameter, indicating when there is a giant component in the graph, and study the size of the largest component by aid of simulations. When the expected degrees in the graph are fixed and the connections are shifted so that more edges connect vertices of different types, we find that the critical parameter decreases. The size of the largest component in the supercritical regime can be both increasing and decreasing as the connections change, depending on the combination of types. For the preferential attachment model, we analyze the degree distributions of the two types and derive explicit expressions for the degree exponents. The exponents are confirmed by simulations that also illustrate other properties of the degree structure.

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A spatial epidemic model with site contamination

We introduce the effect of site contamination in a model for spatial epidemic spread and show that the presence of site contamination may have a strict effect on the model in the sense that it can make an otherwise subcritical process supercritical. Each site on $\mathbb{Z}^d$ is independently assigned a random number of particles and these then perform random walks restricted to bounded regions around their home locations. At time 0, the origin is infected along with all its particles. The infection then spread in that an infected particle that jumps to a new site causes the site along with all particles located there to be infected. Also, a healthy particle that jumps to a site where infection is presents, either in that the site is infected or in the presence of infected particles, becomes infected. Particles and sites recover at rate $λ$ and $γ$, respectively, and then become susceptible to the infection again. We show that, for each given value of $λ$, there is a positive probability that the infection survives indefinitely if $γ$ is sufficiently small, and that, for each given value of $γ$, the infection dies out almost surely if $λ$ is large enough. Several open problems and modifications of the model are discussed, and some natural conjectures are supported by simulations.

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Friendly frogs, stable marriage, and the magic of invariance

We introduce a two-player game involving two tokens located at points of a fixed set. The players take turns to move a token to an unoccupied point in such a way that the distance between the two tokens is decreased. Optimal strategies for this game and its variants are intimately tied to Gale-Shapley stable marriage. We focus particularly on the case of random infinite sets, where we use invariance, ergodicity, mass transport, and deletion-tolerance to determine game outcomes.

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