We state and prove a version for invasion percolation of Schramm and Smirnov's (2001) discrete gluing theorem for critical planar percolation. The result is a first step toward establishing factorization and characterizing noise sensitivity for invasion percolation.
We consider invasion percolation on Galton-Watson trees. On almost every Galton-Watson tree, the invasion cluster almost surely contains only one infinite path. This means that for almost every Galton-Watson tree, invasion percolation induces a probability measure on infinite paths from the root. We show that under certain conditions of the progeny distribution, this measure is absolutely continuous with respect to the limit uniform measure. This confirms that invasion percolation, an efficient self-tuning algorithm, may be used to sample approximately from the limit uniform distribution. Addi…
We compare the probabilities of arm events in two-dimensional invasion percolation to those in critical percolation. Arm events are defined by the existence of a prescribed color sequence of invaded and non-invaded connections from the origin to distance n. We find that, for sequences of a particular form, arm probabilities in invasion percolation and critical percolation are comparable, uniformly in n, while they differ by a power of n for all others. A corollary of our results is the existence, on the triangular lattice, of arm exponents for invasion percolation, for any color sequence with …
In invasion percolation, the edges of successively maximal weight (the outlets) divide the invasion cluster into a chain of ponds separated by outlets. On the regular tree, the ponds are shown to grow exponentially, with law of large numbers, central limit theorem and large deviation results. The tail asymptotics for a fixed pond are also studied and are shown to be related to the asymptotics of a critical percolation cluster, with a logarithmic correction.
We consider invasion percolation on the randomly-weighted complete graph $K_n$, started from some number $k(n)$ of distinct source vertices. The outcome of the process is a forest consisting of $k(n)$ trees, each containing exactly one source. Let $M_n$ be the size of the largest tree in this forest. Logan, Molloy and Pralat (arXiv:1806.10975) proved that if $k(n)/n^{1/3} \to 0$ then $M_n/n \to 1$ in probability. In this paper we prove a complementary result: if $k(n)/n^{1/3} \to \infty$ then $M_n/n \to 0$ in probability. This establishes the existence of a phase transition in the structure of…
We consider invasion percolation on the square lattice. It has been proved by van den Berg, Peres, Sidoravicius and Vares, that the probability that the radius of a so-called pond is larger than n, differs at most a factor of order log n from the probability that in critical Bernoulli percolation the radius of an open cluster is larger than n. We show that these two probabilities are, in fact, of the same order. Moreover, we prove an analogous result for the volume of a pond.
We study invasion percolation in two dimensions. We compare connectivity properties of the origin's invaded region to those of (a) the critical percolation cluster of the origin and (b) the incipient infinite cluster. To exhibit similarities, we show that for any $k\geq1$, the $k$-point function of the first so-called pond has the same asymptotic behavior as the probability that $k$ points are in the critical cluster of the origin. More prominent, though, are the differences. We show that there are infinitely many ponds that contain many large disjoint $p_c$-open clusters. Further, for $k>1$, …
This note is motivated by results in arXiv:math/0608132 and arXiv:0806.2425 about global relations between the invasion percolation cluster (IPC) and the incipient infinite cluster (IIC) on regular trees and on two dimensional lattices, respectively. Namely, that the laws of the two objects are mutually singular, and, in the case of regular trees, that the IIC stochastically dominates the IPC. We prove that on two dimensional lattices, the IIC does not stochastically dominate the IPC. This is the first example showing that the relation between the IIC and IPC is significantly different on tree…
We study invasion percolation in two dimensions, focusing on properties of the outlets of the invasion and their relation to critical percolation and to incipient infinite clusters (IIC's). First we compute the exact decay rate of the distribution of both the weight of the kth outlet and the volume of the kth pond. Next we prove bounds for all moments of the distribution of the number of outlets in an annulus. This result leads to almost sure bounds for the number of outlets in a box B(2^n) and for the decay rate of the weight of the kth outlet to p_c. We then prove existence of multiple-armed…
We prove existence of the scaling limit of the invasion percolation cluster (IPC) on a regular tree. The limit is a random real tree with a single end. The contour and height functions of the limit are described as certain diffusive stochastic processes. This convergence allows us to recover and make precise certain asymptotic results for the IPC. In particular, we relate the limit of the rescaled level sets of the IPC to the local time of the scaled height function.
We derive "quenched" subdiffusive lower bounds for the exit time tau(n) from a box of size n for the simple random walk on the planar invasion percolation cluster. The first part of the paper is devoted to proving an almost sure analog of H. Kesten's subdiffusivity theorem for the random walk on the incipient infinite cluster and the invasion percolation cluster using ideas of M. Aizenman, A. Burchard and A. Pisztora. The proof combines lower bounds on the instrinsic distance in these graphs and general inequalities for reversible Markov chains. In the second part of the paper, we present a sh…
Invasion percolation is a stochastic growth model that follows a greedy algorithm. After assigning i.i.d. uniform random variables (weights) to all edges of $\mathbb{Z}^d$, the growth starts at the origin. At each step, we adjoin to the current cluster the edge of minimal weight from its boundary. In '85, Chayes-Chayes-Newman studied the `acceptance profile' of the invasion: for a given $p \in [0,1]$, it is the ratio of the expected number of invaded edges until time $n$ with weight in $[p,p+\text{d}p]$ to the expected number of observed edges (those in the cluster or its boundary) with weight…
We prove limit theorems and variance estimates for quantities related to ponds and outlets for 2D invasion percolation. We first exhibit several properties of a sequence $({\mathbf{O}}(n))$ of outlet variables, the $n$th of which gives the number of outlets in the box centered at the origin of side length $2^n$. The most important of these properties describes the sequence's renewal structure and exponentially fast mixing behavior. We use these to prove a central limit theorem and strong law of large numbers for $({\mathbf{O}}(n))$. We then show consequences of these limit theorems for the pon…
We study invasion percolation on Aldous' Poisson-weighted infinite tree, and derive two distinct Markovian representations of the resulting process. One of these is the $σ\to\infty$ limit of a representation discovered by Angel et al. [Ann. Appl. Probab. 36 (2008) 420-466]. We also introduce an exploration process of a randomly weighted Poisson incipient infinite cluster. The dynamics of the new process are much more straightforward to describe than those of invasion percolation, but it turns out that the two processes have extremely similar behavior. Finally, we introduce two new "stationary"…
We prove that the Minimal Spanning Tree and the Invasion Percolation Tree on a version of the triangular lattice in the complex plane have unique scaling limits, which are invariant under rotations, scalings, and, in the case of the MST, also under translations. However, they are not expected to be conformally invariant. We also prove some geometric properties of the limiting MST. The topology of convergence is the space of spanning trees introduced by Aizenman, Burchard, Newman & Wilson (1999), and the proof relies on the existence and conformal covariance of the scaling limit of the near-cri…
We consider invasion percolation on a rooted regular tree. For the infinite cluster invaded from the root, we identify the scaling behavior of its $r$-point function for any $r\geq2$ and of its volume both at a given height and below a given height. We find that while the power laws of the scaling are the same as for the incipient infinite cluster for ordinary percolation, the scaling functions differ. Thus, somewhat surprisingly, the two clusters behave differently; in fact, we prove that their laws are mutually singular. In addition, we derive scaling estimates for simple random walk on the …
We use invasion percolation to compute numerical values for bond and site percolation thresholds $p_c$ (existence of an infinite cluster) and $p_u$ (uniqueness of the infinite cluster) of tesselations $\{P,Q\}$ of the hyperbolic plane, where $Q$ faces meet at each vertex and each face is a $P$-gon. Our values are accurate to six or seven decimal places, allowing us to explore their functional dependency on $P$ and $Q$ and to numerically compute critical exponents. We also prove rigorous upper and lower bounds for $p_c$ and $p_u$ that can be used to find the scaling of both thresholds as a func…