Universality for two-dimensional critical cellular automata

In this paper we consider kinetically constrained models (KCM) on $\mathbb Z^2$ with general update families $\mathcal U$. For $\mathcal U$ belonging to the so-called "critical class" our focus is on the divergence of the infection time of the origin for the equilibrium process as the density of the facilitating sites vanishes. In a recent paper Mar\^ech\'e and two of the present authors proved that if $\mathcal U$ has an infinite number of "stable directions", then on a doub...

In this paper a random graph model $G_{\mathbb{Z}^2_N,p_d}$ is introduced, which is a combination of fixed torus grid edges in $(\mathbb{Z}/N \mathbb{Z})^2$ and some additional random ones. The random edges are called long, and the probability of having a long edge between vertices $u,v\in(\mathbb{Z}/N \mathbb{Z})^2$ with graph distance $d$ on the torus grid is $p_d=c/Nd$, where $c$ is some constant. We show that, {\em whp}, the diameter $D(G_{\mathbb{Z}^2_N,p_d})=\Theta (\lo...

Graph bootstrap percolation is a deterministic cellular automaton which was introduced by Bollob\'as in 1968, and is defined as follows. Given a graph $H$, and a set $G \subset E(K_n)$ of initially `infected' edges, we infect, at each time step, a new edge $e$ if there is a copy of $H$ in $K_n$ such that $e$ is the only not-yet infected edge of $H$. We say that $G$ percolates in the $H$-bootstrap process if eventually every edge of $K_n$ is infected. The extremal questions fo...

The aim of this paper is to explore possible ways of extending Smirnov's proof of Cardy's formula for critical site-percolation on the triangular lattice to other cases (such as bond-percolation on the square lattice); the main question we address is that of the choice of the lattice embedding into the plane which gives rise to conformal invariance in the scaling limit. Even though we were not able to produce a complete proof, we believe that the ideas presented here go in th...

We study the percolation time of the $r$-neighbour bootstrap percolation model on the discrete torus $(\Z/n\Z)^d$. For $t$ at most a polylog function of $n$ and initial infection probabilities within certain ranges depending on $t$, we prove that the percolation time of a random subset of the torus is exactly equal to $t$ with high probability as $n$ tends to infinity. Our proof rests crucially on three new extremal theorems that together establish an almost complete understa...

The class of critical bootstrap percolation models in two dimensions was recently introduced by Bollob\'as, Smith and Uzzell, and the critical threshold for percolation was determined up to a constant factor for all such models by the authors of this paper. Here we develop and refine the techniques introduced in that paper in order to determine a sharp threshold for the Duarte model. This resolves a question of Mountford from 1995, and is the first result of its type for a mo...

We argue the exact universal result for the three-point connectivity of critical percolation in two dimensions. Predictions for Potts clusters and for the scaling limit below p_c are also given.

Cellular Automata have been used since their introduction as a discrete tool of modelization. In many of the physical processes one may modelize thus (such as bootstrap percolation, forest fire or epidemic propagation models, life without death, etc), each local change is irreversible. The class of freezing Cellular Automata (FCA) captures this feature. In a freezing cellular automaton the states are ordered and the cells can only decrease their state according to this "freez...

In modified two-neighbour bootstrap percolation in two dimensions each site of $\mathbb Z^2$ is initially independently infected with probability $p$ and on each discrete time step one additionally infects sites with at least two non-opposite infected neighbours. In this note we establish that for this model the second term in the asymptotics of the infection time $\tau$ unexpectedly scales differently from the classical two-neighbour model, in which arbitrary two infected ne...

In the polluted bootstrap percolation model, the vertices of a graph are independently declared initially occupied with probability p or closed with probability q. At subsequent steps, a vertex becomes occupied if it is not closed and it has at least r occupied neighbors. On the cubic lattice Z^d of dimension d>=3 with threshold r=2, we prove that the final density of occupied sites converges to 1 as p and q both approach 0, regardless of their relative scaling. Our result pa...