The maximum time of 2-neighbour bootstrap percolation in grid graphs and some parameterized results

In this paper we focus on $r$-neighbor bootstrap percolation, which is a process on a graph where initially a set $A_0$ of vertices gets infected. Now subsequently, an uninfected vertex becomes infected if it is adjacent to at least $r$ infected vertices. Call $A_f$ the set of vertices that is infected after the process stops. More formally set $A_t:=A_{t-1}\cup \{v\in V: |N(v)\cap A_{t-1}|\geq r\}$, where $N(v)$ is the neighborhood of $v$. Then $A_f=\bigcup_{t>0} A_t$. We de...

Graph bootstrap percolation is a simple cellular automaton introduced by Bollob\'as in 1968. Given a graph $H$ and a set $G \subseteq E(K_n)$ we initially "infect" all edges in $G$ and then, in consecutive steps, we infect every $e \in K_n$ that completes a new infected copy of $H$ in $K_n$. We say that $G$ percolates if eventually every edge in $K_n$ is infected. The extremal question about the size of the smallest percolating sets when $H = K_r$ was answered independently b...

Given a graph $G$ and assuming that some vertices of $G$ are infected, the $r$-neighbor bootstrap percolation rule makes an uninfected vertex $v$ infected if $v$ has at least $r$ infected neighbors. The $r$-percolation number, $m(G,r)$, of $G$ is the minimum cardinality of a set of initially infected vertices in $G$ such that after continuously performing the $r$-neighbor bootstrap percolation rule each vertex of $G$ eventually becomes infected. In this paper, we consider per...

By bootstrap percolation we mean the following deterministic process on a graph $G$. Given a set $A$ of vertices "infected" at time 0, new vertices are subsequently infected, at each time step, if they have at least $r\in\mathbb{N}$ previously infected neighbors. When the set $A$ is chosen at random, the main aim is to determine the critical probability $p_c(G,r)$ at which percolation (infection of the entire graph) becomes likely to occur. This bootstrap process has been ext...

In this paper we fill in a fundamental gap in the extremal bootstrap percolation literature, by providing the first proof of the fact that for all $d \geq 1$, the size of the smallest percolating sets in $d$-neighbour bootstrap percolation on $[n]^d$, the $d$-dimensional grid of size $n$, is $n^{d-1}$. Additionally, we prove that such sets percolate in time at most $c_d n^2$, for some constant $c_d >0 $ depending on $d$ only.

In this paper, we study the k-neighbor bootstrap percolation process on the d-dimensional grid [n]^d, and show that the minimum number of initial vertices that percolate is (1-d/k)n^d + O(n^{d-1})$ when d<=k<=2d. This confirms a conjecture of Pete.

The $r$-neighbour bootstrap percolation process on a graph $G$ starts with an initial set $A_0$ of "infected" vertices and, at each step of the process, a healthy vertex becomes infected if it has at least $r$ infected neighbours (once a vertex becomes infected, it remains infected forever). If every vertex of $G$ eventually becomes infected, then we say that $A_0$ percolates. We prove a conjecture of Balogh and Bollob\'as which says that, for fixed $r$ and $d\to\infty$, ev...

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...

Majority bootstrap percolation is a monotone cellular automata that can be thought of as a model of infection spreading in networks. Starting with an initially infected set, new vertices become infected once more than half of their neighbours are infected. The average case behaviour of this process was studied on the $n$-dimensional hypercube by Balogh, Bollob\'{a}s and Morris, who showed that there is a phase transition as the typical density of the initially infected set in...

Given two graphs $G$ and $H$, it is said that $G$ percolates in $H$-bootstrap process if one could join all the nonadjacent pairs of vertices of $G$ in some order such that a new copy of $H$ is created at each step. Balogh, Bollob\'as and Morris in 2012 investigated the threshold of $H$-bootstrap percolation in the Erd\H{o}s-R\'enyi model for the complete graph $H$ and proposed the similar problem for $H=K_{s,t}$, the complete bipartite graph. In this paper, we provide lower ...