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Let {Zn} be a supercritical Galton–Watson process in varying environments, and W be the limit of the non-negative martingale {Zn/EZn}. Under a condition which ensures that W is not identically equal to zero we give an upper bound on the possible rates of growth of the process on the set {W = 0}, and find a sufficient condition for the process to have only one rate of growth. We also give an example of a process whose offspring distributions have bounded pth moments, for some p > 1, and which has an infinite number of rates of growth.
Multidimensional Markov processes in continuous time with asymptotically linear mean change per unit of time are studied as randomly perturbed linear differential equations. Conditions for exponential and polynomial growth rates with stable type distribution are given. From these conditions results on branching models of populations with stabilizing reproduction for near-supercritical and near-critical cases follow.
By imbedding the multitype version of the standard epidemic model in a multiparameter process, we derive a functional limit theorem for the total cost of the epidemics.
Two urns initially contain r red balls and n – r black balls respectively. At each time epoch a ball is chosen randomly from each urn and the balls are switched. Effectively the same process arises in many other contexts, notably for a symmetric exclusion process and random walk on the Johnson graph. If Y(·) counts the number of black balls in the first urn then we give a direct asymptotic analysis of its transition probabilities to show that (when run at rate (n – r)/n in continuous time) for as n →∞, where π n denotes the equilibrium distribution of Y(·) and γ α = 1 – α /β (1 – β). Thus for large n the transient probabilities approach their equilibrium values at time log n + log|γ α | (≦log n) in a particularly sharp manner. The same is true of the separation distance between the transient distribution and the equilibrium distribution. This is an explicit analysis of the so-called cut-off phenomenon associated with a wide variety of Markov chains.
We characterize the conditions under which an absorbing Markovian finite process (in discrete or continuous time) can be transformed into a new aggregated process conserving the Markovian property, whose states are elements of a given partition of the original state space. To obtain this characterization, a key tool is the quasi-stationary distribution associated with absorbing processes. It allows the absorbing case to be related to the irreducible one. We are able to calculate the set of all initial distributions of the starting process leading to an aggregated homogeneous Markov process by means of a finite algorithm. Finally, it is shown that the continuous-time case can always be reduced to the discrete one using the uniformization technique.
This paper considers the asymptotic distribution of the maximum number of infectives in an epidemic model by showing that, as the initial number of susceptibles converges to infinity, the process of infectives converges almost surely to a birth and death process. The model studied here is more general than usual (see e.g. Bailey (1975), Bharucha-Reid (1960), Keilson (1979)) in that it incorporates immigration and the limiting birth and death process is non-linear. The main novelty of the present paper is the martingale approach used to prove the above-mentioned convergence.
An object is hidden in one of two boxes and occasionally moves between the boxes in accordance with some specified continuous-time Markov process. The objective is to find the object with a minimal expected cost. In this paper it is assumed that search efforts are unlimited. In addition to the search costs, the ‘real time' until the object is found is also taken into account in the cost structure. Our main results are that the optimal policy may consist of five regions and that the controls applied should be of the extreme 0 or ∞ type. The resulting expected cost compares favorably with that of the expected cost with bounded controls studied previously in the search literature.
In the paper, we discuss the properties of Cowan and Mecke's Markov chain P in general form. We give some criteria for determining whether the chain P is transient, recurrent null or recurrent non-null, and for the chain P to have invariant measures.
This paper is concerned with the description of both a deterministic and stochastic branching procedure. The renewal equations for the deterministic branching population are first derived which allow for asymptotic results on the ‘number' and ‘generation' processes. A probabilistic version of these processes is then studied which presents some discrepancy with the standard Harris age-dependent branching processes.
We study convergence in total variation of non-stationary Markov chains in continuous time and apply the results to the image analysis problem of object recognition. The input is a grey-scale or binary image and the desired output is a graphical pattern in continuous space, such as a list of geometric objects or a line drawing. The natural prior models are Markov point processes found in stochastic geometry. We construct well-defined spatial birth-and-death processes that converge weakly to the posterior distribution. A simulated annealing algorithm involving a sequence of spatial birth-and-death processes is developed and shown to converge in total variation to a uniform distribution on the set of posterior mode solutions. The method is demonstrated on a tame example.
This paper introduces exchangeable bisexual models with fixed population sizes and non-overlapping generations. In each generation there are N pairs of individuals consisting of a female and a male. The N pairs of a generation produce N daughters and N sons altogether, and these 2N children form the N pairs of the next generation at random.
First the extinction of the lines of descendants of a fixed number of pairs is studied, when the population size becomes large. Under suitable conditions this structure can be approximately treated in the framework of a Galton-Watson process. In particular it is shown for the Wright-Fisher model that the discrepancy between the extinction probabilities in the model and in the approximating Galton-Watson process is of order N.
Next, the process of the number of ancestor-pairs of all pairs of a generation is analysed. Under suitable conditions this process, properly normed, has a weak limit as N becomes large. For the Wright-Fisher model this limit is an Ornstein–Uhlenbeck process (restricted to a discrete time-set). The corresponding stationary distributions of the backward processes converge to the normal distribution, as expected.
Consider GI/G/1 processor sharing queues with traffic intensity tending to 1. Using the theory of random measures and the theory of branching processes we investigate the limiting behaviour of the queue length, sojourn time and random measures describing attained and residual processing times of customers present.
A Markov-modulated Poisson process (MMPP) is a Poisson process whose rate is a finite Markov chain. The Poisson process is a simple MMPP. An MMPP/M/1 queue is a queue with MMPP arrivals, an infinite capacity, and a single exponential server. We prove that the output of an MMPP/M/1 queue is not an MMPP process unless the input is Poisson. We derive this result by analyzing the structure of the non-linear filter of the state given the departure process of the queue. The practical relevance of the result is that it rules out the existence of simple finite descriptions of queueing networks with MMPP inputs.
Let A be a stochastic matrix and ε a positive number. We consider all stochastic matrices within ε of A and their corresponding stochastic eigenvectors. A convex polytope containing these vectors is described. An efficient algorithm for computing bounds on the components of these vectors is also given. The work is compared to previous such work done by the author and by Courtois and Semai.
This paper examines the infinitely high dam with seasonal (periodic) Lévy input under the unit release rule. We show that a periodic limiting distribution of dam content exists whenever the mean input over a seasonal cycle is less than 1. The Laplace transform of dam content at a finite time and the Laplace transform of the periodic limiting distribution are derived in terms of the probability of an empty dam. Necessary and sufficient conditions for the periodic limiting distribution to have finite moments are given. Convergence rates to the periodic limiting distribution are obtained from the moment results. Our methods of analysis lean heavily on the coupling method and a stochastic monotonicity result.
The continuous autoregressive and minification stationary non-negative time series models discussed by Chernick et al. (1988) are generalized to model marginal distributions which have atoms of mass at zero. The reversibility theorem relating these processes with exponential marginal distributions is extended to the case where the marginal distribution has exponential tail.
In a branching process with random environments, the probability of ultimate extinction is a function of the environment sequence, and is therefore a random variable. Explicit results about the distribution of this random variable are difficult to obtain in general. Here we assume independent and identically distributed environments and use the special properties of fractional linear generating functions to derive some explicit distributions, which may be singular or absolutely continuous, depending on the values of certain parameters. We also consider briefly tail behaviour close to 1, and provide an extension to cases where probability generating functions are not fractional linear.
We consider the Mx/G/∞ queue in which customers in a batch belong to k different types, and a customer of type i requires a non-negative service time with general distribution function Bi(s) (1 ≦ i ≦ k). The number of customers in a batch is stochastic. The joint probability generating function of the number of customers of type i being served at a fixed time t > 0 is derived by the method of collective marks.
We consider a model for the spread of an epidemic through a population divided into m groups, in which infectives move from group to group and infect only within their current group. For both deterministic and stochastic versions of this model, the effect on the total size of the epidemic of varying the speed with which infectives move between groups is considered. We also compare the distribution of the total size of this model with that of a suitably matched model in which infectives cannot move between groups, but are able to infect outside their own group.