The height of random kk-trees and related branching processes

We consider the height of random k-trees and k-Apollonian networks. These random graphs are not really trees, but instead have a tree-like structure. The height will be the maximum distance of a vertex from the root. We show that w.h.p. the height of random k-trees and k-Apollonian networks is asymptotic to clog t, where t is the number of vertices, and c=c(k) is given as the solution to a transcendental equation. The equations are slightly different for the two types of process. In the limit as k-->oo the height of both processes is asymptotic to log t/(k log 2)

Random real trees

We survey recent developments about random real trees, whose prototype is the Continuum Random Tree (CRT) introduced by Aldous in 1991. We briefly explain the formalism of real trees, which yields a neat presentation of the theory and in particular of the relations between discrete Galton-Watson trees and continuous random trees. We then discuss the particular class of self-similar random real trees called stable trees, which generalize the CRT. We review several important results concerning stable trees, including their branching property, which is analogous to the well-known property of Galton-Watson trees, and the calculation of their fractal dimension. We then consider spatial trees, which combine the genealogical structure of a real tree with spatial displacements, and we explain their connections with superprocesses. In the last section, we deal with a particular conditioning problem for spatial trees, which is closely related to asymptotics for random planar quadrangulations.Comment: 25 page

Fringe trees, Crump-Mode-Jagers branching processes and mm-ary search trees

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 of random trees, where the theory is developed in detail. In particular, we consider fringe trees of $m$-ary search trees in detail; this seems to be new. Various applications are given, including degree distribution, protected nodes and maximal clades for various types of random trees. Again, we emphasise results for $m$-ary search trees, and give for example new results on protected nodes in $m$-ary search trees. A separate section surveys results on height, saturation level, typical depth and total path length, due to Devroye (1986), Biggins (1995, 1997) and others. This survey contains well-known basic results together with some additional general results as well as many new examples and applications for various classes of random trees

The coalescent point process of branching trees

We define a doubly infinite, monotone labeling of Bienayme-Galton-Watson (BGW) genealogies. The genealogy of the current generation backwards in time is uniquely determined by the coalescent point process $(A_i; i\ge 1)$, where $A_i$ is the coalescence time between individuals i and i+1. There is a Markov process of point measures $(B_i; i\ge 1)$ keeping track of more ancestral relationships, such that $A_i$ is also the first point mass of $B_i$. This process of point measures is also closely related to an inhomogeneous spine decomposition of the lineage of the first surviving particle in generation h in a planar BGW tree conditioned to survive h generations. The decomposition involves a point measure $\rho$ storing the number of subtrees on the right-hand side of the spine. Under appropriate conditions, we prove convergence of this point measure to a point measure on $\mathbb{R}_+$ associated with the limiting continuous-state branching (CSB) process. We prove the associated invariance principle for the coalescent point process, after we discretize the limiting CSB population by considering only points with coalescence times greater than $\varepsilon$.Comment: Published in at http://dx.doi.org/10.1214/11-AAP820 the Annals of Applied Probability (http://www.imstat.org/aap/) by the Institute of Mathematical Statistics (http://www.imstat.org

The structure of the allelic partition of the total population for Galton-Watson processes with neutral mutations

We consider a (sub) critical Galton-Watson process with neutral mutations (infinite alleles model), and decompose the entire population into clusters of individuals carrying the same allele. We specify the law of this allelic partition in terms of the distribution of the number of clone-children and the number of mutant-children of a typical individual. The approach combines an extension of Harris representation of Galton-Watson processes and a version of the ballot theorem. Some limit theorems related to the distribution of the allelic partition are also given.Comment: This version corrects a significant mistake in the first on