August 27, 2015
In 2-neighborhood bootstrap percolation on a graph $G$, an infection spreads according to the following deterministic rule: infected vertices of $G$ remain infected forever and in consecutive rounds healthy vertices with at least two already infected neighbors become infected. Percolation occurs if eventually every vertex is infected. The maximum time $t(G)$ is the maximum number of rounds needed to eventually infect the entire vertex set. In 2013, it was proved by Benevides et al \cite{eurocomb13} that $t(G)$ is NP-hard for planar graphs and that deciding whether $t(G)\geq k$ is polynomial time solvable for $k\leq 2$, but is NP-complete for $k\geq 4$. They left two open problems about the complexity for $k=3$ and for planar bipartite graphs. In 2014, we solved the first problem\cite{wg2014}. In this paper, we solve the second one by proving that $t(G)$ is NP-complete even in grid graphs with maximum degree 3. We also prove that $t(G)$ is polynomial time solvable for solid grid graphs with maximum degree 3. Moreover, we prove that the percolation time problem is W[1]-hard on the treewidth of the graph, but it is fixed parameter tractable with parameters treewidth$+k$ and maxdegree$+k$.
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August 27, 2015
In 2-neighborhood bootstrap percolation on a graph G, an infection spreads according to the following deterministic rule: infected vertices of G remain infected forever and in consecutive rounds healthy vertices with at least 2 already infected neighbors become infected. Percolation occurs if eventually every vertex is infected. The maximum time t(G) is the maximum number of rounds needed to eventually infect the entire vertex set. In 2013, it was proved \cite{eurocomb13} tha...
We consider a classic model known as bootstrap percolation on the $n \times n$ square grid. To each vertex of the grid we assign an initial state, infected or healthy, and then in consecutive rounds we infect every healthy vertex that has at least $2$ already infected neighbours. We say that percolation occurs if the whole grid is eventually infected. In this paper, contributing to a recent series of extremal results in this field, we prove that the maximum time a bootstrap p...
September 15, 2022
For $r\geq1$, the $r$-neighbour bootstrap process in a graph $G$ starts with a set of infected vertices and, in each time step, every vertex with at least $r$ infected neighbours becomes infected. The initial infection percolates if every vertex of $G$ is eventually infected. We exactly determine the minimum cardinality of a set that percolates for the $3$-neighbour bootstrap process when $G$ is a $3$-dimensional grid with minimum side-length at least $11$. We also characteri...
July 26, 2023
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 th...
July 28, 2017
In $r$-neighbour bootstrap percolation, vertices (sites) of a graph $G$ are infected, round-by-round, if they have $r$ neighbours already infected. Once infected, they remain infected. An initial set of infected sites is said to percolate if every site is eventually infected. We determine the maximal percolation time for $r$-neighbour bootstrap percolation on the hypercube for all $r \geq 3$ as the dimension $d$ goes to infinity up to a logarithmic factor. Surprisingly, it tu...
September 22, 2023
Bootstrap Percolation is a process defined on a graph which begins with an initial set of infected vertices. In each subsequent round, an uninfected vertex becomes infected if it is adjacent to at least $r$ previously infected vertices. If an initially infected set of vertices, $A_0$, begins a process in which every vertex of the graph eventually becomes infected, then we say that $A_0$ percolates. In this paper we investigate bootstrap percolation as it relates to graph dist...
May 17, 2012
In r-neighbour bootstrap percolation on the vertex set of a graph G, vertices are initially infected independently with some probability p. At each time step, the infected set expands by infecting all uninfected vertices that have at least r infected neighbours. We study the distribution of the time t at which all vertices become infected. Given t = t(n) = o(log n/log log n), we prove a sharp threshold result for the probability that percolation occurs by time t in d-neighbou...
November 5, 2019
This paper is dedicated to the study of the interaction between dynamical systems and percolation models, with views towards the study of viral infections whose virus mutate with time. Recall that r-bootstrap percolation describes a deterministic process where vertices of a graph are infected once r neighbors of it are infected. We generalize this by introducing F(t)-bootstrap percolation, a time-dependent process where the number of neighbouring vertices which need to be inf...
October 21, 2015
The process of $H$-bootstrap percolation for a graph $H$ is a cellular automaton, where, given a subset of the edges of $K_n$ as initial set, an edge is added at time $t$ if it is the only missing edge in a copy of $H$ in the graph obtained through this process at time $t-1$. We discuss an extremal question about the time of $K_r$-bootstrap percolation, namely determining maximal times for an $n$-vertex graph before the process stops. We determine exact values for $r=4$ and f...
August 25, 2015
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 ...