In standard bootstrap percolation, a subset A of the n x n grid is initially infected. A new site is then infected if at least two of its neighbours are infected, and an infected site stays infected forever. The set A is said to percolate if eventually the entire grid is infected. A percolating set is said to be minimal if none of its subsets percolate. Answering a question of Bollobas, we show that there exists a minimal percolating set of size 4n^2/33 + o(n^2), but there does not exist one larger than (n + 2)^2/6.
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.
For any integer $r\geqslant0$, the $r$-neighbor bootstrap percolation on a graph is an activation process of the vertices. The process starts with some initially activated vertices and then, in each round, any inactive vertex with at least $r$ active neighbors becomes activated. A set of initially activated vertices leading to the activation of all vertices is said to be a percolating set. Denote the minimum size of a percolating set in the $r$-neighbor bootstrap percolation process on a graph $G$ by $m(G, r)$. In this paper, we present upper and lower bounds on $m(K_n^d, r)$, where $K_n^d$ is…
The $r$-neighbour bootstrap process is an update rule for the states of vertices in which `uninfected' vertices with at least $r$ `infected' neighbours become infected and a set of initially infected vertices is said to \emph{percolate} if eventually all vertices are infected. For every $r \geq 3$, a sharp condition is given for the minimum degree of a sufficiently large graph that guarantees the existence of a percolating set of size $r$. In the case $r=3$, for $n$ large enough, any graph on $n$ vertices with minimum degree $\lfloor n/2 \rfloor +1$ has a percolating set of size $3$ and for $r…
We study combinatorial parameters of a recently introduced bootstrap percolation problem in finite projective planes. We present sharp results on the size of the minimum percolating sets and the maximal non-percolating sets. Additional results on the minimal and maximal percolation time as well as on the critical probability in the projective plane are also presented.
The $r$-neighbour bootstrap process describes an infection process on a graph, where we start with a set of initially infected vertices and an uninfected vertex becomes infected as soon as it has $r$ infected neighbours. An inital set of infected vertices is called percolating if at the end of the bootstrap process all vertices are infected. We give Ore-type conditions that guarantee the existence of a small percolating set of size $l\leq 2r-2$ if the number of vertices $n$ of our graph is sufficiently large: if $l\geq r$ and satisfies $2r \geq l+2 \lfloor \sqrt{2(l-r)+0.25}+2.5 \rfloor-1$ the…
We introduce a simple method for proving lower bounds for the size of the smallest percolating set in a certain graph bootstrap process. We apply this method to determine the sizes of the smallest percolating sets in multidimensional tori and multidimensional grids (in particular hypercubes). The former answers a question of Morrison and Noel, and the latter provides an alternative and simpler proof for one of their main results.
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 infected for a disease to be transmitted is determined by a percolation function F(t) at each time t. After studying some o…
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 Bollobás which says that, for fixed $r$ and $d\to\infty$, every percolating set in the $d$-dimensional hypercube has cardinality at least $\frac{1+o(1)}{r}\binom{d}{r-1}$. We also prov…
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 percolation process can take to eventually infect the entire vertex set of the grid is $13n^2/18+O(n)$.
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, Bollobás and Morris in 2012 investigated the threshold of $H$-bootstrap percolation in the Erdős-Rényi 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 and upper bounds on the threshold of $K_{2, t}$-bootstrap percolation. In addition, a threshold function is derived for $K_{2, 4…
In $\HH$-bootstrap percolation, a set $A \subset V(\HH)$ of initially 'infected' vertices spreads by infecting vertices which are the only uninfected vertex in an edge of the hypergraph $\HH$. A particular case of this is the $H$-bootstrap process, in which $\HH$ encodes copies of $H$ in a graph $G$. We find the minimum size of a set $A$ that leads to complete infection when $G$ and $H$ are powers of complete graphs and $\HH$ encodes induced copies of $H$ in $G$. The proof uses linear algebra, a technique that is new in bootstrap percolation, although standard in the study of weakly saturated …
Motivated by the bootstrap percolation process for graphs, we define a new, high-order generalisation to $k$-uniform hypergraphs, in which we infect $j$-sets of vertices for some integer $1\le j \le k-1$. We investigate the smallest possible size of an initially infected set which ultimately percolates and determine the exact size in almost all cases of $k$ and $j$.
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.
Bootstrap percolation on a graph with infection threshold $r\in \mathbb{N}$ is an infection process, which starts from a set of initially infected vertices and in each step every vertex with at least $r$ infected neighbours becomes infected. We consider bootstrap percolation on the binomial random graph $G(n,p)$, which was investigated among others by Janson, Łuczak, Turova and Valier (2012). We improve their results by strengthening the probability bounds for the number of infected vertices at the end of the process.
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 turns out to be $\frac{2^d}{d}$, which is in great contrast with the value for $r=2$, which is quadratic in $d$, as establ…
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 find a lower bound for the asymptotics for $r \geq 5$ by giving an explicit construction.
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.
We study the distribution of the percolation time $T$ of two-neighbour bootstrap percolation on $[n]^2$ with initial set $A\sim\mathrm{Bin}([n]^2,p)$. We determine $T$ with high probability up to a constant factor for all $p$ above the critical probability for percolation, and to within a $1+o(1)$ factor for a large range of $p$.
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 Bollobás, Gunderson, Holmgren, Janson and Przykucki. We also show that these bounds are best possible up to positive constants not depending on the offspring distribution.
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 Erdős-Rényi 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, Bollobás, and Morris. We also establish a general lower bound of the percolation threshold for all $K_{r,s}$, with $r\geq s \geq 3$.
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 understanding of the geometric behaviour of the $r$-neighbour bootstrap process in the dense setting. The special case $d-r=0$ o…
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-neighbour bootstrap percolation on the d-dimensional discrete torus T_n^d. Moreover, we show that for certain ranges of p = p(n)…
In this note we provide an alternative proof of the fact that subcritical bootstrap percolation models have a positive critical probability in any dimension. The proof relies on a recent extension of the classical framework of Toom. This approach is not only simpler than the original multi-scale renormalisation proof of the result in two and more dimensions, but also gives significantly better bounds. As a byproduct, we improve the best known bounds for the stability threshold of Toom's North-East-Center majority rule cellular automaton.
We study an extremal question for the (reversible) $r-$bootstrap percolation processes. Given a graph and an initial configuration where each vertex is active or inactive, in the $r-$bootstrap percolation process the following rule is applied in discrete-time rounds: each vertex gets active if it has at least $r$ active neighbors, and an active vertex stays active forever. In the reversible $r$-bootstrap percolation, each vertex gets active if it has at least $r$ active neighbors, and inactive otherwise. We consider the following question on the $d$-dimensional torus: how many vertices should …
Graph bootstrap percolation, introduced by Bollobás in 1968, is a cellular automaton defined as follows. Given a "small" graph $H$ and a "large" graph $G = G_0 \subseteq K_n$, in consecutive steps we obtain $G_{t+1}$ from $G_t$ by adding to it all new edges $e$ such that $G_t \cup e$ contains a new copy of $H$. We say that $G$ percolates if for some $t \geq 0$, we have $G_t = K_n$. For $H = K_r$, the question about the size of the smallest percolating graphs was independently answered by Alon, Frankl and Kalai in the 1980's. Recently, Balogh, Bollobás and Morris considered graph bootstrap perc…
We generalize and improve results of Andrews, Gravner, Holroyd, Liggett, and Romik on metastability thresholds for generalized two-dimensional bootstrap percolation models, and answer several of their open problems and conjectures. Specifically, we prove slow convergence and localization bounds for Holroyd, Liggett, and Romik's k-percolation models, and in the process provide a unified and improved treatment of existing results for bootstrap, modified bootstrap, and Frobose percolation. Furthermore, we prove improved asymptotic bounds for the generating functions of partitions without k-gaps, …
On a geometric model for complex networks (introduced by Krioukov et al.) we investigate the bootstrap percolation process. This model consists of random geometric graphs on the hyperbolic plane having $N$ vertices, a dependent version of the Chung-Lu model. The process starts with infection rate $p=p(N)$. Each uninfected vertex with at least $\mathbf{r}\geq 1$ infected neighbors becomes infected, remaining so forever. We identify a function $p_c(N)=o(1)$ such that a.a.s.\ when $p\gg p_c(N)$ the infection spreads to a positive fraction of vertices, whereas when $p\ll p_c(N)$ the process cannot…
We investigate bootstrap percolation with infection threshold $r> 1$ on the binomial $k$-uniform random hypergraph $H_k(n,p)$ in the regime $n^{-1}\ll n^{k-2}p \ll n^{-1/r}$, when the initial set of infected vertices is chosen uniformly at random from all sets of given size. We establish a threshold such that if there are less vertices in the initial set of infected vertices, then whp only a few additional vertices become infected, while if the initial set of infected vertices exceeds the threshold then whp almost every vertex becomes infected. In addition, for $k=2$, we show that the probabil…
We study the critical probability for the metastable phase transition of the two-dimensional anisotropic bootstrap percolation model with $(1,2)$-neighbourhood and threshold $r = 3$. The first order asymptotics for the critical probability were recently determined by the first and second authors. Here we determine the following sharp second and third order asymptotics: \[ p_c\big( [L]^2,\mathcal{N}_{(1,2)},3 \big) \; = \; \frac{(\log \log L)^2}{12\log L} \, - \, \frac{\log \log L \, \log \log \log L}{ 3\log L} + \frac{\left(\log \frac{9}{2} + 1 \pm o(1) \right)\log \log L}{6\log L}. \] We note…
Graph bootstrap percolation is a deterministic cellular automaton which was introduced by Bollobás 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 for this model, when $H$ is the complete graph $K_r$, were solved (independently) by Alon, Kalai and Frankl almost thirty ye…
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. Vertices are initially infected independently at random and the central question is whether all vertices eventually becom…
Two-dimensional bootstrap percolation is a cellular automaton in which sites become 'infected' by contact with two or more already infected nearest neighbors. We consider these dynamics, which can be interpreted as a monotone version of the Ising model, on an n x n square, with sites initially infected independently with probability p. The critical probability p_c is the smallest p for which the probability that the entire square is eventually infected exceeds 1/2. Holroyd determined the sharp first-order approximation: p_c \sim π^2/(18 log n) as n \to \infty. Here we sharpen this result, prov…
Geometric inhomogeneous random graphs (GIRGs) are a model for scale-free networks with underlying geometry. We study bootstrap percolation on these graphs, which is a process modelling the spread of an infection of vertices starting within a (small) local region. We show that the process exhibits a phase transition in terms of the initial infection rate in this region. We determine the speed of the process in the supercritical case, up to lower order terms, and show that its evolution is fundamentally influenced by the underlying geometry. For vertices with given position and expected degree, …
Bootstrap percolation models have been extensively studied during the two past decades. In this article, we study the following "anisotropic" bootstrap percolation model: the neighborhood of a point (m,n) is the set \[\{(m+2,n),(m+1,n),(m,n+1),(m-1,n),(m-2,n),(m,n-1)\}.\] At time 0, sites are occupied with probability p. At each time step, sites that are occupied remain occupied, while sites that are not occupied become occupied if and only if three of more sites in their neighborhood are occupied. We prove that it exhibits a sharp metastability threshold. This is the first mathematical proof …
Bootstrap percolation is a class of cellular automata with random initial state. Two-dimensional bootstrap percolation models have three rough universality classes, the most studied being the `critical' one. For this class the scaling of the quantity of greatest interest -- the critical probability -- was determined by Bollobás, Duminil-Copin, Morris and Smith in terms of a simply defined combinatorial quantity called `difficulty', so the subject seemed closed up to finding sharper results. However, the computation of the difficulty, was never considered. In this paper we provide the first alg…
Consider the following model of strong-majority bootstrap percolation on a graph. Let r be some positive integer, and p in [0,1]. Initially, every vertex is active with probability p, independently from all other vertices. Then, at every step of the process, each vertex v of degree deg(v) becomes active if at least (deg(v)+r)/2 of its neighbours are active. Given any arbitrarily small p>0 and any integer r, we construct a family of d=d(p,r)-regular graphs such that with high probability all vertices become active in the end. In particular, the case r=1 answers a question and disproves a conjec…
