The branching-ruin number of a tree, which describes its asymptotic growth and geometry, can be seen as a polynomial version of the branching number. This quantity was defined by Collevecchio, Kious and Sidoravicius (2018) in order to understand the phase transitions of the once-reinforced random walk (ORRW) on trees. Strikingly, this number was proved to be equal to the critical parameter of ORRW on trees. In this paper, we continue the investigation of the link between the branching-ruin number and the criticality of random processes on trees. First, we study random walks on random conductances on trees, when the conductances have an heavy tail at $0$, parametrized by some $p>1$, where $1/p$ is the exponent of the tail. We prove a phase transition recurrence/transience with respect to $p$ and identify the critical parameter to be equal to the branching-ruin number of the tree. Second, we study a multi-excited random walk on trees where each vertex has $M$ cookies and each cookie has an infinite strength towards the root. Here again, we prove a phase transition recurrence/transience and identify the critical number of cookies to be equal to the branching-ruin number of the tree, minus 1. This result extends a conjecture of Volkov (2003). Besides, we study a generalized version of this process and generalize results of Basdevant and Singh (2009).
The motivation for this paper is the study of the phase transition for recurrence/transience of a class of self-interacting random walks on trees, which includes the once-reinforced random walk. For this purpose, we define a quantity, that we call the branching-ruin number of a tree, which provides (in the spirit of Furstenberg, 1970, and Lyons, 1990) a natural way to measure trees with polynomial growth. We prove that the branching-ruin number of a tree is equal to the critical parameter for the recurrence/transience of the once-reinforced random walk. We define a sharp and effective (i.e. co…
The goal of these lectures is to survey some of the recent progress on the description of large-scale structure of random trees. We use the framework of Markov-Branching sequences of trees and discuss several applications.
We consider branching random walks and contact processes on infinite, connected, locally finite graphs whose reproduction and infectivity rates across edges are inversely proportional to vertex degree. We show that when the ambient graph is a Galton-Watson tree then, in certain circumstances, the branching random walks and contact processes will have weak survival phases. We also provide bounds on critical values.
We study the local convergence of critical Galton-Watson trees and Levy trees under various conditionings. Assuming a very general monotonicity property on the functional of random trees, we show that random trees conditioned to have large functional values always converge locally to immortal trees. We also derive a very general ratio limit property for functionals of random trees satisfying the monotonicity property. Then we move on to study the local convergence of critical continuous-state branching processes, and prove a similar result. Finally we give a definition of continuum condensatio…
We generalize recent results of Haas and Miermont to obtain scaling limits of Markov branching trees whose size is specified by the number of nodes whose out-degree lies in a given set. We then show that this implies that the scaling limit of finite variance Galton-Watson trees condition on the number of nodes whose out-degree lies in a given set is the Brownian continuum random tree. The key to this is a generalization of the classical Otter-Dwass formula.
We introduce a simple tree growth process that gives rise to a new two-parameter family of discrete fragmentation trees that extends Ford's alpha model to multifurcating trees and includes the trees obtained by uniform sampling from Duquesne and Le Gall's stable continuum random tree. We call these new trees the alpha-gamma trees. In this paper, we obtain their splitting rules, dislocation measures both in ranked order and in sized-biased order, and we study their limiting behaviour.
By studying an admissible family of branching mechanisms introduced in Li (2014), we obtain a pruning procedure on Lévy trees. Then we could construct a decreasing Lévy-CRT-valued process $\{{\mathcal T}_t\}$ by pruning Lévy trees and an analogous process $\{{\mathcal T}^*_t\}$ by pruning a critical Lévy tree conditioned to be infinite. Under a regular condition on the admissible family of branching mechanisms, we show that the law of $\{{\mathcal T}_t\}$ at the ascension time can be represented by $\{{\mathcal T}^*_t\}$. The results generalize those studied in Abraham and Delmas (2012).
This paper considers linear functions constructed on two different weighted branching processes and provides explicit bounds for their Kantorovich-Rubinstein distance in terms of couplings of their corresponding generic branching vectors. Motivated by applications to the analysis of random graphs, we also consider a variation of the weighted branching process where the generic branching vector has a different dependence structure from the usual one. By applying the bounds to sequences of weighted branching processes, we derive sufficient conditions for the convergence in the Kantorovich-Rubins…
We consider a family of random trees satisfying a Markov branching property. Roughly, this property says that the subtrees above some given height are independent with a law that depends only on their total size, the latter being either the number of leaves or vertices. Such families are parameterized by sequences of distributions on partitions of the integers that determine how the size of a tree is distributed in its different subtrees. Under some natural assumption on these distributions, stipulating that "macroscopic" splitting events are rare, we show that Markov branching trees admit the…
We introduce flows of branching processes with competition, which describe the evolution of general continuous state branching populations in which interactions between individuals give rise to a negative density dependence term. This generalizes the logistic branching processes studied by Lambert. Following the approach developed by Dawson and Li, we first construct such processes as the solutions of certain flow of stochastic differential equations. We then propose a novel genealogical description for branching processes with competition based on interactive pruning of Lévy-trees, and establ…
We define a multi-type coalescent point process of a general branching process with finitely many types. This multi-type coalescent fully describes the genealogy of the (quasi-stationary) standing population, providing types along ancestral lineages of all individuals in the standing population. We show that this point-process is a functional of a certain Markov chain defined by the planar embedding of the branching process. This Markov chain is further used to determine statistical properties of the ancestral tree, such as the time to the most recent common ancestor (MRCA) of two consecutive …
We consider a model of stationary population with random size given by a continuous state branching process with immigration with a quadratic branching mechanism. We give an exact elementary simulation procedure of the genealogical tree of $n$ individuals randomly chosen among the extant population at a given time. Then, we prove the convergence of the renormalized total length of this genealogical tree as $n$ goes to infinity, see also Pfaffelhuber, Wakolbinger and Weisshaupt (2011) in the context of a constant size population. The limit appears already in Bi and Delmas (2016) but with a diff…
We prove the existence of the total length process for the genealogical tree of a population model with random size given by a quadratic stationary continuous-state branching processes. We also give, for the one-dimensional marginal, its Laplace transform as well as the fluctuation of the corresponding convergence. This result is to be compared with the one obtained by Pfaffelhuber and Wakolbinger for constant size population associated to the Kingma coalescent. We also give a time reversal property of the number of ancestors process at all time, and give a description of the so-called lineage…
We are interested in the genealogical structure of alleles for a Bienaymé-Galton-Watson branching process with neutral mutations (infinite alleles model), in the situation where the initial population is large and the mutation rate small. We shall establish that for an appropriate regime, the process of the sizes of the allelic sub-families converges in distribution to a certain continuous state branching process (i.e. a Jirina process) in discrete time. Itô's excursion theory and the Léevy-Itô decomposition of subordinators provide fundamental insights for the results.
Continuous-time branching processes (CTBPs) are powerful tools in random graph theory, but are not appropriate to describe real-world networks, since they produce trees rather than (multi)graphs. In this paper we analyze collapsed branching processes (CBPs), obtained by a collapsing procedure on CTBPs, in order to define multigraphs where vertices have fixed out-degree $m\geq 2$. A key example consists of preferential attachment models (PAMs), as well as generalized PAMs where vertices are chosen according to their degree and age. We identify the degree distribution of CBPs, showing that it is…
Generalized gamma distributions arise as limits in many settings involving random graphs, walks, trees, and branching processes. Peköz, Röllin, and Ross (2016, arXiv:1309.4183 [math.PR]) exploited characterizing distributional fixed point equations to obtain uniform error bounds for generalized gamma approximations using Stein's method. Here we show how monotone couplings arising with these fixed point equations can be used to obtain sharper tail bounds that, in many cases, outperform competing moment-based bounds and the uniform bounds obtainable with Stein's method. Applications are given to…
This survey studies asymptotics of random fringe trees and extended fringe trees in random trees that can be constructed as family trees of a Crump-Mode-Jagers branching process, stopped at a suitable time. This includes random recursive trees, preferential attachment trees, fragmentation trees, binary search trees and (more generally) $m$-ary search trees, as well as some other classes of random trees. We begin with general results, mainly due to Aldous (1991) and Jagers and Nerman (1984). The general results are applied to fringe trees and extended fringe trees for several particular types o…
We consider random recursive trees that are grown via community modulated schemes that involve random attachment or degree based attachment. The aim of this paper is to derive general techniques based on continuous time embedding to study such models. The associated continuous time embeddings are not branching processes: individual reproductive rates at each time depend on the composition of the entire population at that time. Using stochastic analytic techniques we show that various key macroscopic statistics of the continuous time embedding stabilize, allowing asymptotics for a host of funct…
Let $T$ be the regular tree in which every vertex has exactly $d\ge 3$ neighbours. Run a branching random walk on $T$, in which at each time step every particle gives birth to a random number of children with mean $d$ and finite variance, and each of these children moves independently to a uniformly chosen neighbour of its parent. We show that, starting with one particle at some vertex $0$ and conditionally on survival of the process, the time it takes for every vertex within distance $r$ of $0$ to be hit by a particle of the branching random walk is almost surely $r + \frac{2}{\log(3/2)}\log\…
We are interested in the local limits of families of random trees that satisfy the Markov branching property, which is fulfilled by a wide range of models. Loosely, this property entails that given the sizes of the sub-trees above the root, these sub-trees are independent and their distributions only depend upon their respective sizes. The laws of the elements of a Markov branching family are characterised by a sequence of probability distributions on the sets of integer partitions which describes how the sizes of the sub-trees above the root are distributed. We prove that under some natural a…
A class of branching processes in varying environments is exhibited which become extinct almost surely even though the means M_n grow fast enough so that sum M_n^{-1} is finite. In fact, such a process is constructed for every offspring distribution of infinite variance, and this establishes the converse of a previously known fact: that if a distribution has finite variance then sum M_n^{-1}=infty is equivalent to almost sure extinction. This has as an immediate consequence the converse to a theorem on equipolarity of Galton-Watson trees.
We study a genealogical model for continuous-state branching processes with immigration with a (sub)critical branching mechanism. This model allows the immigrants to be on the same line of descent. The corresponding family tree is an ordered rooted continuum random tree with a single infinite end defined thanks to two continuous processes denoted by $(\overleftarrow{H}_t ;t\geq 0)$ and $(\overrightarrow{H}_t ;t\geq 0)$ that code the parts at resp. the left and the right hand of the infinite line of descent of the tree. These processes are called the left and the right height processes. We defi…
We establish a second-order almost sure limit theorem for the minimal position in a one-dimensional super-critical branching random walk, and also prove a martingale convergence theorem which answers a question of Biggins and Kyprianou [9]. Our method applies furthermore to the study of directed polymers on a disordered tree. In particular, we give a rigorous proof of a phase transition phenomenon for the partition function (from the point of view of convergence in probability), already described by Derrida and Spohn [17]. Surprisingly, this phase transition phenomenon disappears in the sense …
The reproduction speed of a continuous-time branching random walk is proportional to a positive parameter $λ$. There is a threshold for $λ$, which is called $λ_w$, that separates almost sure global extinction from global survival. Analogously, there exists another threshold $λ_s$ below which any site is visited almost surely a finite number of times (i.e.~local extinction) while above it there is a positive probability of visiting every site infinitely many times. The local critical parameter $λ_s$ is completely understood and can be computed as a function of the reproduction rates. On the oth…
The Horton and Tokunaga branching laws provide a convenient framework for studying self-similarity in random trees. The Horton self-similarity is a weaker property that addresses the principal branching in a tree; it is a counterpart of the power-law size distribution for elements of a branching system. The stronger Tokunaga self-similarity addresses so-called side branching. The Horton and Tokunaga self-similarity have been empirically established in numerous observed and modeled systems, and proven for two paradigmatic models: the critical Galton-Watson branching process with finite progeny …
We introduce a model of branching interlacements for general critical offspring distributions. It consists of a countable collection of infinite tree-indexed random walk trajectories on $Z^d,d\geq5$. We show that this model turns out to be the local limit of the tree-indexed random walk in a discrete torus, conditioned on the size proportional to the volume of the torus. This generalizes the previous results of Angel, Ráth and the author, for the critical geometric offspring distribution. Our model also includes the model of random interlacements introduced by Sznitman as a degenerate case. To…
We investigate the genealogical structure of general critical or subcritical continuous-state branching processes. Analogously to the coding of a discrete tree by its contour function, this genealogical structure is coded by a real-valued stochastic process called the height process, which is itself constructed as a local time functional of a Levy process with no negative jumps. We present a detailed study of the height process and of an associated measure-valued process called the exploration process, which plays a key role in most applications. Under suitable assumptions, we prove that whene…
A decomposable strongly critical Galton-Watson branching process with $N$ types of particles labelled $1,2,...,N$ is considered in which a type~$i$ parent may produce individuals of types $j\geq i$ only. This model may be viewed as a stochastic model for the sizes of a geographically structured population occupying $N$ islands, the location of a particle being considered as its type. The newborn particles of island $i\leq N-1$ either stay at the same island or migrate, just after their birth to the islands $% i+1,i+2,...,N$. Particles of island $N$ do not migrate. We investigate the structure …
We are interested in predator-prey dynamics on infinite trees, which can informally be seen as particular two-type branching processes where individuals may die (or be infected) only after their parent dies (or is infected). We study two types of such dynamics: the chase-escape process, introduced by Kordzakhia with a variant by Bordenave, and the birth-and-assassination process, introduced by Aldous & Krebs. We exhibit a coupling between these processes and branching random walks starting from a random point and killed at the barrier 0. This sheds new light on the chase-escape and birth-and-a…
Consider a rooted infinite Galton-Watson tree with mean offspring number $m>1$, and a collection of i.i.d. positive random variables $ξ_e$ indexed by all the edges in the tree. We assign the resistance $m^d ξ_e$ to each edge $e$ at distance $d$ from the root. In this random electric network, we study the asymptotic behavior of the effective resistance and conductance between the root and the vertices at depth $n$. Our results generalize an existing work of Addario-Berry, Broutin and Lugosi on the binary tree to random branching networks.
We consider a model of random tree growth, where at each time unit a new vertex is added and attached to an already existing vertex chosen at random. The probability with which a vertex with degree $k$ is chosen is proportional to $w(k)$, where the weight function $w$ is the parameter of the model. In the papers of B. Bollobas, O. Riordan, J. Spencer, G. Tusnady, and, independently, Mori, the asymptotic degree distribution is obtained for a model that is equivalent to the special case of ours, when the weight function is linear. The proof therein strongly relies on the linear choice of $w$. We…
We introduce multi-type Markov Branching trees, which are simple random population tree models where individuals are characterized by their size and type and give rise to (size,type)-children in a Galton-Watson fashion, with the rule that the size of any individual is a least the sum of the sizes of its children. Assuming that macroscopic size-splittings are rare, we describe the scaling limits of multi-type Markov Branching trees in terms of multi-type self-similar fragmentation trees. We observe three different regimes according to whether the probability of type change of a size-biased chil…
In this paper, we show that a Galton-Watson tree conditioned to have a fixed number of particles in generation $n$ converges in distribution as $n\rightarrow\infty$, and with this tool we study the span and gap statistics of a branching random walk on such trees, which is the discrete version of Ramola, Majumdar and Schehr 2015, generalized to arbitrary offspring and displacement distributions with moment constraints.
We show that the transience or recurrence of a random walk in certain random environments on an arbitrary infinite locally finite tree is determined by the branching number of the tree, which is a measure of the average number of branches per vertex. This generalizes and unifies previous work of the authors. It also shows that the point of phase transition for edge-reinforced random walk is likewise determined by the branching number of the tree. Finally, we show that the branching number determines the rate of first-passage percolation on trees, also known as the first-birth problem. Our tech…
A particular continuous-time multitype branching process is considered, it is the continuous-time embedding of a discrete-time process which is very popular in theoretical computer science: the m-ary search tree (m is an integer). There is a well-known phase transition: when m \leq 26, the asymptotic behavior of the process is Gaussian, but for m \geq 27 it is no more Gaussian and a limit W of a complex-valued martingale arises. Thanks to the branching property it appears as a solution of a smoothing equation of the type Z = e^{-λT}(Z(1) + ... + Z(m)), where λ \in C, the Z(k) are independent c…
In the first part of this paper we give easy and intuitive proofs for the small value probabilities of the martingale limit of a supercritical Galton-Watson process in both the Schröder and the Böttcher case. These results are well-known, but the most cited proofs rely on generating function arguments which are hard to transfer to other settings. In the second part we show that the strategy underlying our proofs can be used in the quite different context of self-intersections of stochastic processes. Solving a problem posed by Wenbo Li, we find the small value probabilities for intersection lo…
We obtain a representation of Feller's branching diffusion with logistic growth in terms of the local times of a reflected Brownian motion $H$ with a drift that is affine linear in the local time accumulated by $H$ at its current level. As in the classical Ray-Knight representation, the excursions of $H$ are the exploration paths of the trees of descendants of the ancestors at time $t=0$, and the local time of $H$ at height $t$ measures the population size at time $t$ (see e.g. \cite{LG4}). We cope with the dependence in the reproduction by introducing a pecking order of individuals: an indivi…
Consider a general branching process, a.k.a. Crump-Mode-Jagers process, generated by a perturbed random walk $η_1$, $ξ_1+η_2$, $ξ_1+ξ_2+η_3,\ldots$. Here, $(ξ_1,η_1)$, $(ξ_2, η_2),\ldots$ are independent identically distributed random vectors with arbitrarily dependent positive components. Denote by $N_j(t)$ the number of the $j$th generation individuals with birth times $\leq t$. Assume that $j=j(t)\to\infty$ and $j(t)=o(t^a)$ as $t\to\infty$ for some explicitly given $a>0$ (to be specified in the paper). The corresponding $j$th generation belongs to the set of intermediate generations. We pr…
In this work, we give a description of all sigma-finite measures on the space of rooted compact real trees which satisfy a certain regenerative property. We show that any infinite measure which satisfies the regenerative property is the "law" of a Levy tree, that is, the "law" of a tree-valued random variable that describes the genealogy of a population evolving according to a continuous-state branching process. On the other hand, we prove that a probability measure with the regenerative property must be the law of the genealogical tree associated with a continuous-time discrete-state branchin…
We consider the Brownian tree introduced by Aldous and the associated Q-process which consists in an infinite spine on which are grafted independent Brownian trees. We present a reversal procedure on these trees that consists in looking at the tree downward from its top: the branching points becoming leaves and leaves becoming branching points. We prove that the distribution of the tree is invariant under this reversal procedure, which provides a better understanding of previous results from Bi and Delmas (2016).
We consider the genealogical tree of a stationary continuous state branching process with immigration. For a sub-critical stable branching mechanism, we consider the genealogical tree of the extant population at some fixed time and prove that, up to a deterministic time-change, it is distributed as a continuous-time Galton-Watson process with immigration. We obtain similar results for a critical stable branching mechanism when only looking at immigrants arriving in some fixed time-interval. For a general sub-critical branching mechanism, we consider the number of individuals that give descenda…
We consider so-called discrete snakes obtained from size-conditioned critical Bienaymé-Galton-Watson trees by assigning to each node a random spatial position in such a way that the increments along each edge are i.i.d. When the offspring distribution belongs to the domain of attraction of a stable law with index $α\in (1,2]$, we give a necessary and sufficient condition on the tail distribution of the spatial increments for this spatial tree to converge, in a functional sense, towards the Brownian snake driven by the $α$-stable Lévy tree. We also study the case of heavier tails, and apply our…
We study branching diffusions in a bounded domain $D$ of $\mathbb{R}^d$ in which particles are killed upon hitting the boundary $\partial D$. It is known that any such process undergoes a phase transition when the branching rate $β$ exceeds a critical value: a multiple of the first eigenvalue of the generator of the diffusion. We investigate the system at criticality and show that the associated genealogical tree, when the process is conditioned to survive for a long time, converges to Aldous' Continuum Random Tree under appropriate rescaling. The result holds under only a mild assumption on t…
Rooted, weighted continuum random trees are used to describe limits of sequences of random discrete trees. Formally, they are random quadruples $(\mathcal{T},d,r,p)$, where $(\mathcal{T},d)$ is a tree-like metric space, $r\in\mathcal{T}$ is a distinguished root, and $p$ is a probability measure on this space. The underlying branching structure is carried implicitly in the metric $d$. We explore various ways of describing the interaction between branching structure and mass in $(\mathcal{T},d,r,p)$ in a way that depends on $d$ only by way of this branching structure. We introduce a notion of ma…
We consider a branching random walk (BRW) taking its values in the $\mathtt{b}$-ary rooted tree $\mathbb W_{ \mathtt{b}}$ (i.e. the set of finite words written in the alphabet $\{ 1, \ldots, \mathtt{b} \}$, with $\mathtt{b}\! \geq \! 2$). The BRW is indexed by a critical Galton--Watson tree conditioned to have $n$ vertices; its offspring distribution is aperiodic and is in the domain of attraction of a $γ$-stable law, $γ\in (1, 2]$. The jumps of the BRW are those of a nearest-neighbour null-recurrent random walk on $\mathbb W_{ \mathtt{b}}$ (reflection at the root of $\mathbb W_{ \mathtt{b}}$ …
