An Improved Upper Bound for Bootstrap Percolation in All Dimensions

Answering questions of Itai Benjamini, we show that the event of complete occupation in 2-neighbour bootstrap percolation on the d-dimensional box [n]^d, for d\geq 2, at its critical initial density p_c(n), is noise sensitive, while in k-neighbour bootstrap percolation on the d-regular random graph G_{n,d}, for 2\leq k\leq d-2, it is insensitive. Many open problems remain.

Bootstrap percolation is a cellular automaton modelling the spread of an `infection' on a graph. In this note, we prove a family of lower bounds on the critical probability for $r$-neighbour bootstrap percolation on Galton--Watson trees in terms of moments of the offspring distributions. With this result we confirm a conjecture of Bollob\'as, Gunderson, Holmgren, Janson and Przykucki. We also show that these bounds are best possible up to positive constants not depending on t...

We study bootstrap percolation processes on random simplicial complexes of some fixed dimension $d \geq 3$. Starting from a single simplex of dimension $d$, we build our complex dynamically in the following fashion. We introduce new vertices one by one, all equipped with a random weight from a fixed distribution $\mu$. The newly arriving vertex selects an existing $(d-1)$-dimensional face at random, with probability proportional to some positive and symmetric function $f$ of ...

Bootstrap percolation has been used effectively to model phenomena as diverse as emergence of magnetism in materials, spread of infection, diffusion of software viruses in computer networks, adoption of new technologies, and emergence of collective action and cultural fads in human societies. It is defined on an (arbitrary) network of interacting agents whose state is determined by the state of their neighbors according to a threshold rule. In a typical setting, bootstrap per...

An upper bound for the critical probability of long range bond percolation in $d=2$ and $d=3$ is obtained by connecting the bond percolation with the SIR epidemic model, thus complementing the lower bound result in Frei and Perkins arXiv:arch-ive/1603.04130. A key ingredient is that we establish a uniform bound for the local times of branching random walk by calculating their exponential moments and by using the discrete versions of Tanaka's formula and Garsia's Lemma.

A graph $G$ percolates in the $K_{r,s}$-bootstrap process if we can add all missing edges of $G$ in some order such that each edge creates a new copy of $K_{r,s}$, where $K_{r,s}$ is the complete bipartite graph. We study $K_{r,s}$-bootstrap percolation on the Erd\H{o}s-R\'{e}nyi random graph, and determine the percolation threshold for balanced $K_{r,s}$ up to a logarithmic factor. This partially answers a question raised by Balogh, Bollob\'as, and Morris. We also establish ...

Bootstrap percolation is a type of cellular automaton on graphs, introduced as a simple model of the dynamics of ferromagnetism. Vertices in a graph can be in one of two states: `healthy' or `infected' and from an initial configuration of states, healthy vertices become infected by local rules. While the usual bootstrap processes are monotone in the sets of infected vertices, in this paper, a modification is examined in which infected vertices can return to a healthy state. V...

We consider a dynamical process on a graph $G$, in which vertices are infected (randomly) at a rate which depends on the number of their neighbours that are already infected. This model includes bootstrap percolation and first-passage percolation as its extreme points. We give a precise description of the evolution of this process on the graph $\mathbb{Z}^2$, significantly sharpening results of Dehghanpour and Schonmann. In particular, we determine the typical infection time ...

Let $d\ge 3$ be a fixed integer, $p\in (0,1)$, and let $n\geq 1$ be a positive integer such that $dn$ is even. Let $\mathbb{G}(n, d, p)$ be a (random) graph on $n$ vertices obtained by drawing uniformly at random a $d$-regular (simple) graph on $[n]$ and then performing independent $p$-bond percolation on it, i.e. we independently retain each edge with probability $p$ and delete it with probability $1-p$. Let $|\mathcal{C}_{\text{max}}|$ be the size of the largest component i...

Consider a $p$-random subset $A$ of initially infected vertices in the discrete cube $[L]^3$, and assume that the neighbourhood of each vertex consists of the $a_i$ nearest neighbours in the $\pm e_i$-directions for each $i \in \{1,2,3\}$, where $a_1\le a_2\le a_3$. Suppose we infect any healthy vertex $x\in [L]^3$ already having $a_3+1$ infected neighbours, and that infected sites remain infected forever. In this paper we determine the critical length for percolation up to a...