We consider linear-fractional branching processes (one-type and two-type) with immigration in varying environments. For $n\ge0$, let $Z_n$ count the number of individuals of the nth generation, which excludes the immigrant who enters the system at time n. We call n a regeneration time if $Z_n=0$. For both the one-type and two-type cases, we give criteria for the finiteness or infiniteness of the number of regeneration times. We then construct some concrete examples to exhibit the strange phenomena caused by the so-called varying environments. For example, it may happen that the process is extinct, but there are only finitely many regeneration times. We also study the asymptotics of the number of regeneration times of the model in the example.

We show joint convergence of the Łukasiewicz path and height process for slightly supercritical Galton–Watson forests. This shows that the height processes for supercritical continuous-state branching processes as constructed by Lambert (2002) are the limit under rescaling of their discrete counterparts. Unlike for (sub-)critical Galton–Watson forests, the height process does not encode the entire metric structure of a supercritical Galton–Watson forest. We demonstrate that this result is nonetheless useful, by applying it to the configuration model with an independent and identically distributed power-law degree sequence in the critical window, of which we obtain the metric space scaling limit in the product Gromov–Hausdorff–Prokhorov topology, which is of independent interest.

During an epidemic outbreak, typically only partial information about the outbreak is known. A common scenario is that the infection times of individuals are unknown, but individuals, on displaying symptoms, are identified as infectious and removed from the population. We study the distribution of the number of infectives given only the times of removals in a Markovian susceptible–infectious–removed (SIR) epidemic. Primary interest is in the initial stages of the epidemic process, where a branching (birth–death) process approximation is applicable. We show that the number of individuals alive in a time-inhomogeneous birth–death process at time $t \geq 0$, given only death times up to and including time t, is a mixture of negative binomial distributions, with the number of mixing components depending on the total number of deaths, and the mixing weights depending upon the inter-arrival times of the deaths. We further consider the extension to the case where some deaths are unobserved. We also discuss the application of the results to control measures and statistical inference.

We study propagation of avalanches in a certain excitable network. The model is a particular case of the one introduced by Larremore et al. (Phys. Rev. E, 2012) and is mathematically equivalent to an endemic variation of the Reed–Frost epidemic model introduced by Longini (Math. Biosci., 1980). Two types of heuristic approximation are frequently used for models of this type in applications: a branching process for avalanches of a small size at the beginning of the process and a deterministic dynamical system once the avalanche spreads to a significant fraction of a large network. In this paper we prove several results concerning the exact relation between the avalanche model and these limits, including rates of convergence and rigorous bounds for common characteristics of the model.

We study continuous-time birth–death type processes, where individuals have independent and identically distributed lifetimes, according to a random variable Q, with E[Q] = 1, and where the birth rate if the population is currently in state (has size) n is α(n). We focus on two important examples, namely α(n) = λ n being a branching process, and α(n) = λn(N - n) / N which corresponds to an SIS (susceptible → infective → susceptible) epidemic model in a homogeneously mixing community of fixed size N. The processes are assumed to start with a single individual, i.e. in state 1. Let T, An, C, and S denote the (random) time to extinction, the total time spent in state n, the total number of individuals ever alive, and the sum of the lifetimes of all individuals in the birth–death process, respectively. We give expressions for the expectation of all these quantities and show that these expectations are insensitive to the distribution of Q. We also derive an asymptotic expression for the expected time to extinction of the SIS epidemic, but now starting at the endemic state, which is not independent of the distribution of Q. The results are also applied to the household SIS epidemic, showing that, in contrast to the household SIR (susceptible → infective → recovered) epidemic, its threshold parameter R* is insensitive to the distribution of Q.

We consider a threshold epidemic model on a clustered random graph model obtained from local transformations in an alternating branching process that approximates a bipartite graph. In other words, our epidemic model is such that an individual becomes infected as soon as the proportion of his/her infected neighbors exceeds the threshold q of the epidemic. In our random graph model, each individual can belong to several communities. The distributions for the community sizes and the number of communities an individual belongs to are arbitrary. We consider the case where the epidemic starts from a single individual, and we prove a phase transition (when the parameter q of the model varies) for the appearance of a cascade, i.e. when the epidemic can be propagated to an infinite part of the population. More precisely, we show that our epidemic is entirely described by a multi-type (and alternating) branching process, and then we apply Sevastyanov's theorem about the phase transition of multi-type Galton-Watson branching processes. In addition, we compute the entries of the mean progeny matrix corresponding to the epidemic. The phase transition for the contagion is given in terms of the largest eigenvalue of this matrix.

The iterative division of a triangle by chords which join a randomly-selected vertex of a triangle to the opposite side is investigated. Results on the limiting random graph which eventuates are given. Aspects studied are: the order of vertices; the fragmentation of chords; age distributions for elements of the graph; various topological characterisations of the triangles. Different sampling protocols are explored. Extensive use is made of the theory of branching processes.

In this article we obtain rates of convergence to equilibrium of marked Hawkes processes in two situations. Firstly, the stationary process is the empty process, in which case we speak of the rate of extinction. Secondly, the stationary process is the unique stationary and nontrivial marked Hawkes process, in which case we speak of the rate of installation. The first situation models small epidemics, whereas the results in the second case are useful in deriving stopping rules for simulation algorithms of Hawkes processes with random marks.

The paper is concerned with filtering the cardinality of a branching process observing the cardinality of a subpopulation. In this model, both the processes, state and observation are pure jump processes and may have common jump times. Preliminary properties are studied in the tree framework. A recursive structure for the filtering equation is proved in the supercritical case.

This paper investigates the relation between a branching process and a non-linear dynamical system in $\mathbb{C}^2$. This idea has previously been fruitful in many investigations, including that of the FKPP equation by McKean, Neveu, Bramson, and others. Our concerns here are somewhat different from those in other work: we wish to elucidate those features of the dynamical system which correspond to the long-term behaviour of the random process. In particular, we are interested in how the dimension of the global attractor corresponds to that of the tail $\sigma$-algebra of the process. The Poincar\'e--Dulac operator which (locally) intertwines the non-linear system with its linearization may sometimes be exhibited as a Fourier--Laplace transform of tail-measurable random variables; but things change markedly when parameters cross values giving the `primary resonance' in the Poincar\'e--Dulac sense. Probability proves effective in establishing {\it global} properties amongst which is a clear description of the global convergence to the attractor. Several of our probabilistic results are analogues of ones obtained by Kesten and Stigum, and by Athreya and Ney, for discrete branching processes. Our simpler context allows the use of It\^o calculus. Because the paper bridges two subjects, dynamical-system theory and probability theory, we take considerable care with the exposition of both aspects. For probabilist readers, we provide a brief guide to Poincar\'e--Dulac theory; and we take the view that in a paper which we hope will be read by analysts, it would be wrong to fudge any details of rigour in our probabilistic arguments. 1991 Mathematics Subject Classification: 60H30, 60J85, 34A20.

We prove some limit theorems for contiunous time and state branching processes. The non-degenerate limit laws are obtained in critical and non-critical cases by conditioning or introducing immigration processes. The limit laws in non-critical cases are characterized in terms of the cononical measure of the cumulant semigroup. The proofs are based on estimates of the cumulant semigroup derived from the forward and backward equations, which are easier than the proffs in the classical setting.

This paper considers a branching process generated by an offspring distribution F with mean m < ∞ and variance σ2 < ∞ and such that, at each generation n, there is an observed δ-migration, according to a binomial law Bpvn*Nnbef which depends on the total population size Nnbef. The δ-migration is defined as an emigration, an immigration or a null migration, depending on the value of δ, which is assumed constant throughout the different generations. The process with δ-migration is a generation-dependent Galton-Watson process, whereas the observed process is not in general a martingale. Under the assumption that the process with δ-migration is supercritical, we generalize for the observed migrating process the results relative to the Galton-Watson supercritical case that concern the asymptotic behaviour of the process and the estimation of m and σ2, as n → ∞. Moreover, an asymptotic confidence interval of the initial population size is given.

Let {Ai : i ≥ 1} be a sequence of non-negative random variables and let M be the class of all probability measures on [0,∞]. Define a transformation T on M by letting Tμ be the distribution of ∑i=1∞AiZi, where the Zi are independent random variables with distribution μ, which are also independent of {Ai}. Under first moment assumptions imposed on {Ai}, we determine exactly when T has a non-trivial fixed point (of finite or infinite mean) and we prove that all fixed points have regular variation properties; under moment assumptions of order 1 + ε, ε > 0, we find all the fixed points and we prove that all non-trivial fixed points have stable-like tails. Convergence theorems are given to ensure that each non-trivial fixed point can be obtained as a limit of iterations (by T) with an appropriate initial distribution; convergence to the trivial fixed points δ0 and δ∞ is also examined, and a result like the Kesten-Stigum theorem is established in the case where the initial distribution has the same tails as a stable law. The problem of convergence with an arbitrary initial distribution is also considered when there is no non-trivial fixed point. Our investigation has applications in the study of: (a) branching processes; (b) invariant measures of some infinite particle systems; (c) the model for turbulence of Yaglom and Mandelbrot; (d) flows in networks and Hausdorff measures in random constructions; and (e) the sorting algorithm Quicksort. In particular, it turns out that the basic functional equation in the branching random walk always has a non-trivial solution.

A filtering problem for a branching process is studied within the tree framework, and the minimal intensity of the splitting process is given.

Whole genome amplification is important for multipoint mapping by sperm or oocyte typing and genetic disease diagnosis. Polymerase chain reaction is not suitable for amplifying long DNA sequences. This paper studies a new technique, designated PEP-primer-extension-preamplification, for amplifying long DNA sequences using the theory of branching processes. A mathematical model for PEP is constructed and a closed formula for the expected target yield is obtained. A central limit theorem and a strong law of large numbers for the number of kth generation target sequences are proved.

This paper deals with a Bienaymé-Galton-Watson process having a random number of ancestors. Its asymptotic properties are studied when both the number of ancestors and the number of generations tend to infinity. This yields consistent and asymptotically normal estimators of the mean and the offspring distribution of the process. By exhibiting a connection with the BGW process with immigration, all results can be transported to the immigration case, under an appropriate sampling scheme. A key feature of independent interest is a new limit theorem for sums of a random number of random variables, which extends the Gnedenko and Fahim (1969) transfer theorem.