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Persistent Betti numbers are a major tool in persistent homology, a subfield of topological data analysis. Many tools in persistent homology rely on the properties of persistent Betti numbers considered as a two-dimensional stochastic process $ (r,s) \mapsto n^{-1/2} (\beta^{r,s}_q ( \mathcal{K}(n^{1/d} \mathcal{X}_n))-\mathbb{E}[\beta^{r,s}_q ( \mathcal{K}( n^{1/d} \mathcal{X}_n))])$. So far, pointwise limit theorems have been established in various settings. In particular, the pointwise asymptotic normality of (persistent) Betti numbers has been established for stationary Poisson processes and binomial processes with constant intensity function in the so-called critical (or thermodynamic) regime; see Yogeshwaran et al. (Prob. Theory Relat. Fields167, 2017) and Hiraoka et al. (Ann. Appl. Prob.28, 2018).
In this contribution, we derive a strong stabilization property (in the spirit of Penrose and Yukich, Ann. Appl. Prob.11, 2001) of persistent Betti numbers, and we generalize the existing results on their asymptotic normality to the multivariate case and to a broader class of underlying Poisson and binomial processes. Most importantly, we show that multivariate asymptotic normality holds for all pairs (r, s), $0\le r\le s<\infty$, and that it is not affected by percolation effects in the underlying random geometric graph.
We investigate the hyperuniformity of marked Gibbs point processes that have weak dependencies among distant points whilst the interactions of close points are kept arbitrary. Various stability and range assumptions are imposed on the Papangelou intensity in order to prove that the resulting point process is not hyperuniform. The scope of our results covers many frequently used models, including Gibbs point processes with a superstable, lower-regular, integrable pair potential, as well as the Widom–Rowlinson model with random radii and Gibbs point processes with interactions based on Voronoi tessellations and nearest-neighbour graphs.
Given a sequence of independent random vectors taking values in ${\mathbb R}^d$ and having common continuous distribution function F, say that the $n^{\rm \scriptsize}$th observation sets a (Pareto) record if it is not dominated (in every coordinate) by any preceding observation. Let $p_n(F) \equiv p_{n, d}(F)$ denote the probability that the $n^{\rm \scriptsize}$th observation sets a record. There are many interesting questions to address concerning pn and multivariate records more generally, but this short paper focuses on how pn varies with F, particularly if, under F, the coordinates exhibit negative dependence or positive dependence (rather than independence, a more-studied case). We introduce new notions of negative and positive dependence ideally suited for such a study, called negative record-setting probability dependence (NRPD) and positive record-setting probability dependence (PRPD), relate these notions to existing notions of dependence, and for fixed $d \geq 2$ and $n \geq 1$ prove that the image of the mapping pn on the domain of NRPD (respectively, PRPD) distributions is $[p^*_n, 1]$ (resp., $[n^{-1}, p^*_n]$), where $p^*_n$ is the record-setting probability for any continuous F governing independent coordinates.
As a generalization of random recursive trees and preferential attachment trees, we consider random recursive metric spaces. These spaces are constructed from random blocks, each a metric space equipped with a probability measure, containing a labelled point called a hook, and assigned a weight. Random recursive metric spaces are equipped with a probability measure made up of a weighted sum of the probability measures assigned to its constituent blocks. At each step in the growth of a random recursive metric space, a point called a latch is chosen at random according to the equipped probability measure, and a new block is chosen at random and attached to the space by joining together the latch and the hook of the block. We use martingale theory to prove a law of large numbers and a central limit theorem for the insertion depth, the distance from the master hook to the latch chosen. We also apply our results to further generalizations of random trees, hooking networks, and continuous spaces constructed from line segments.
We establish power-series expansions for the asymptotic expectations of the vertex number and missed area of random disc-polygons in planar convex bodies with $C^{k+1}_+$-smooth boundaries. These results extend asymptotic formulas proved in Fodor et al. (2014).
A version of the classical Buffon problem in the plane naturally extends to the setting of any Riemannian surface with constant Gaussian curvature. The Buffon probability determines a Buffon deficit. The relationship between Gaussian curvature and the Buffon deficit is similar to the relationship that the Bertrand–Diguet–Puiseux theorem establishes between Gaussian curvature and both circumference and area deficits.
We consider Gaussian approximation in a variant of the classical Johnson–Mehl birth–growth model with random growth speed. Seeds appear randomly in $\mathbb{R}^d$ at random times and start growing instantaneously in all directions with a random speed. The locations, birth times, and growth speeds of the seeds are given by a Poisson process. Under suitable conditions on the random growth speed, the time distribution, and a weight function $h\;:\;\mathbb{R}^d \times [0,\infty) \to [0,\infty)$, we prove a Gaussian convergence of the sum of the weights at the exposed points, which are those seeds in the model that are not covered at the time of their birth. Such models have previously been considered, albeit with fixed growth speed. Moreover, using recent results on stabilization regions, we provide non-asymptotic bounds on the distance between the normalized sum of weights and a standard Gaussian random variable in the Wasserstein and Kolmogorov metrics.
We consider the minimum spanning tree problem on a weighted complete bipartite graph $K_{n_R, n_B}$ whose $n=n_R+n_B$ vertices are random, i.i.d. uniformly distributed points in the unit cube in $d$ dimensions and edge weights are the $p$-th power of their Euclidean distance, with $p\gt 0$. In the large $n$ limit with $n_R/n \to \alpha _R$ and $0\lt \alpha _R\lt 1$, we show that the maximum vertex degree of the tree grows logarithmically, in contrast with the classical, non-bipartite, case, where a uniform bound holds depending on $d$ only. Despite this difference, for $p\lt d$, we are able to prove that the total edge costs normalized by the rate $n^{1-p/d}$ converge to a limiting constant that can be represented as a series of integrals, thus extending a classical result of Avram and Bertsimas to the bipartite case and confirming a conjecture of Riva, Caracciolo and Malatesta.
We determine almost sure limits of rescaled intrinsic volumes of the construction steps of fractal percolation in ${\mathbb R}^d$ for any dimension $d\geq 1$. We observe a factorization of these limit variables which allows one, in particular, to determine their expectations and covariance structure. We also show the convergence of the rescaled expectations and variances of the intrinsic volumes of the construction steps to the expectations and variances of the limit variables, and we give rates for this convergence in some cases. These results significantly extend our previous work, which addressed only limits of expectations of intrinsic volumes.
Processes of random tessellations of the Euclidean space $\mathbb{R}^d$, $d\geq 1$, are considered that are generated by subsequent division of their cells. Such processes are characterized by the laws of the life times of the cells until their division and by the laws for the random hyperplanes that divide the cells at the end of their life times. The STIT (STable with respect to ITerations) tessellation processes are a reference model. In the present paper a generalization concerning the life time distributions is introduced, a sufficient condition for the existence of such cell division tessellation processes is provided, and a construction is described. In particular, for the case that the random dividing hyperplanes have a Mondrian distribution—which means that all cells of the tessellations are cuboids—it is shown that the intrinsic volumes, except the Euler characteristic, can be used as the parameter for the exponential life time distribution of the cells.
Stationary Poisson processes of lines in the plane are studied, whose directional distributions are concentrated on $k\geq 3$ equally spread directions. The random lines of such processes decompose the plane into a collection of random polygons, which form a so-called Poisson line tessellation. The focus of this paper is to determine the proportion of triangles in such tessellations, or equivalently, the probability that the typical cell is a triangle. As a by-product, a new deviation of Miles’s classical result for the isotropic case is obtained by an approximation argument.
The Minkowski functionals, including the Euler characteristic statistics, are standard tools for morphological analysis in cosmology. Motivated by cosmic research, we examine the Minkowski functional of the excursion set for an isotropic central limit random field, whose k-point correlation functions (kth-order cumulants) have the same structure as that assumed in cosmic research. Using 3- and 4-point correlation functions, we derive the asymptotic expansions of the Euler characteristic density, which is the building block of the Minkowski functional. The resulting formula reveals the types of non-Gaussianity that cannot be captured by the Minkowski functionals. As an example, we consider an isotropic chi-squared random field and confirm that the asymptotic expansion accurately approximates the true Euler characteristic density.
We use Stein’s method to establish the rates of normal approximation in terms of the total variation distance for a large class of sums of score functions of samples arising from random events driven by a marked Poisson point process on $\mathbb{R}^d$. As in the study under the weaker Kolmogorov distance, the score functions are assumed to satisfy stabilisation and moment conditions. At the cost of an additional non-singularity condition, we show that the rates are in line with those under the Kolmogorov distance. We demonstrate the use of the theorems in four applications: Voronoi tessellations, k-nearest-neighbours graphs, timber volume, and maximal layers.
We prove that if a unimodular random graph is almost surely planar and has finite expected degree, then it has a combinatorial embedding into the plane which is also unimodular. This implies the claim in the title immediately by a theorem of Angel, Hutchcroft, Nachmias and Ray [2]. Our unimodular embedding also implies that all the dichotomy results of [2] about unimodular maps extend in the one-ended case to unimodular random planar graphs.
We study the large-volume asymptotics of the sum of power-weighted edge lengths $\sum_{e \in E}|e|^\alpha$ in Poisson-based spatial random networks. In the regime $\alpha > d$, we provide a set of sufficient conditions under which the upper-large-deviation asymptotics are characterized by a condensation phenomenon, meaning that the excess is caused by a negligible portion of Poisson points. Moreover, the rate function can be expressed through a concrete optimization problem. This framework encompasses in particular directed, bidirected, and undirected variants of the k-nearest-neighbor graph, as well as suitable $\beta$-skeletons.
Following Bradonjić and Saniee, we study a model of bootstrap percolation on the Gilbert random geometric graph on the 2-dimensional torus. In this model, the expected number of vertices of the graph is n, and the expected degree of a vertex is $a\log n$ for some fixed $a>1$. Each vertex is added with probability p to a set $A_0$ of initially infected vertices. Vertices subsequently become infected if they have at least $ \theta a \log n $ infected neighbours. Here $p, \theta \in [0,1]$ are taken to be fixed constants.
We show that if $\theta < (1+p)/2$, then a sufficiently large local outbreak leads with high probability to the infection spreading globally, with all but o(n) vertices eventually becoming infected. On the other hand, for $ \theta > (1+p)/2$, even if one adversarially infects every vertex inside a ball of radius $O(\sqrt{\log n} )$, with high probability the infection will spread to only o(n) vertices beyond those that were initially infected.
In addition we give some bounds on the $(a, p, \theta)$ regions ensuring the emergence of large local outbreaks or the existence of islands of vertices that never become infected. We also give a complete picture of the (surprisingly complex) behaviour of the analogous 1-dimensional bootstrap percolation model on the circle. Finally we raise a number of problems, and in particular make a conjecture on an ‘almost no percolation or almost full percolation’ dichotomy which may be of independent interest.
This paper addresses the asymptotic analysis of sojourn functionals of spatiotemporal Gaussian random fields with long-range dependence (LRD) in time, also known as long memory. Specifically, reduction theorems are derived for local functionals of nonlinear transformation of such fields, with Hermite rank $m\geq 1,$ under general covariance structures. These results are proven to hold, in particular, for a family of nonseparable covariance structures belonging to the Gneiting class. For $m=2,$ under separability of the spatiotemporal covariance function in space and time, the properly normalized Minkowski functional, involving the modulus of a Gaussian random field, converges in distribution to the Rosenblatt-type limiting distribution for a suitable range of values of the long-memory parameter.
One way to model telecommunication networks are static Boolean models. However, dynamics such as node mobility have a significant impact on the performance evaluation of such networks. Consider a Boolean model in $\mathbb {R}^d$ and a random direction movement scheme. Given a fixed time horizon $T>0$, we model these movements via cylinders in $\mathbb {R}^d \times [0,T]$. In this work, we derive central limit theorems for functionals of the union of these cylinders. The volume and the number of isolated cylinders and the Euler characteristic of the random set are considered and give an answer to the achievable throughput, the availability of nodes, and the topological structure of the network.
Let
$n\geq 2$
random lines intersect a planar convex domain D. Consider the probabilities
$p_{nk}$
,
$k=0,1, \ldots, {n(n-1)}/{2}$
that the lines produce exactly k intersection points inside D. The objective is finding
$p_{nk}$
through geometric invariants of D. Using Ambartzumian’s combinatorial algorithm, the known results are instantly reestablished for
$n=2, 3$
. When
$n=4$
, these probabilities are expressed by new invariants of D. When D is a disc of radius r, the simplest forms of all invariants are found. The exact values of
$p_{3k}$
and
$p_{4k}$
are established.
We derive three critical exponents for Bernoulli site percolation on the uniform infinite planar triangulation (UIPT). First, we compute explicitly the probability that the root cluster is infinite. As a consequence, we show that the off-critical exponent for site percolation on the UIPT is $\beta = 1/2$. Then we establish an integral formula for the generating function of the number of vertices in the root cluster. We use this formula to prove that, at criticality, the probability that the root cluster has at least n vertices decays like $n^{-1/7}$. Finally, we also derive an expression for the law of the perimeter of the root cluster and use it to establish that, at criticality, the probability that the perimeter of the root cluster is equal to n decays like $n^{-4/3}$. Among these three exponents, only the last one was previously known. Our main tools are the so-called gasket decomposition of percolation clusters, generic properties of random Boltzmann maps, and analytic combinatorics.