Asymptotic properties of the stationary measure of a Markov branching process

1973 ◽  
Vol 10 (2) ◽  
pp. 447-450 ◽  
Author(s):  
Y. S. Yang

The asymptotic properties of the unique stationary measure of a Markov branching process will be given. In the critical case with finite variance, the result can be deduced from a result for discrete time processes of Kesten, Ney and Spitzer (1966) where the proof makes use of a stronger assumption than the finiteness of variance. For the continuous time case where the stationary measure has an explicit form, we can use the discrete renewal theorem which takes care of the infinite variance case as well.

1973 ◽  
Vol 10 (02) ◽  
pp. 447-450 ◽  
Author(s):  
Y. S. Yang

The asymptotic properties of the unique stationary measure of a Markov branching process will be given. In the critical case with finite variance, the result can be deduced from a result for discrete time processes of Kesten, Ney and Spitzer (1966) where the proof makes use of a stronger assumption than the finiteness of variance. For the continuous time case where the stationary measure has an explicit form, we can use the discrete renewal theorem which takes care of the infinite variance case as well.


1975 ◽  
Vol 7 (03) ◽  
pp. 495-510
Author(s):  
Carla Lipow

A continuous-time Markov branching process is modified to allow some dependence of offspring generating function on population size. The model involves a given population size M, below which the offspring generating function is supercritical and above which it is subcritical. Immigration is allowed when the population size is 0. The process has a stationary measure, and an expression for its generating function is found. A limit theorem for the stationary measure as M tends to ∞ is then obtained.


1975 ◽  
Vol 7 (3) ◽  
pp. 495-510 ◽  
Author(s):  
Carla Lipow

A continuous-time Markov branching process is modified to allow some dependence of offspring generating function on population size. The model involves a given population size M, below which the offspring generating function is supercritical and above which it is subcritical. Immigration is allowed when the population size is 0. The process has a stationary measure, and an expression for its generating function is found. A limit theorem for the stationary measure as M tends to ∞ is then obtained.


1973 ◽  
Vol 5 (1) ◽  
pp. 37-54 ◽  
Author(s):  
Norman Kaplan

A population model is constructed which combines the ideas of a discrete time branching process with random environments and a continuous time non-homogeneous Markov branching process. The extinction problem is considered and necessary and sufficient conditions for extinction are determined. Also discussed are limit theorems for what corresponds to the supercritical case.


1973 ◽  
Vol 5 (01) ◽  
pp. 37-54 ◽  
Author(s):  
Norman Kaplan

A population model is constructed which combines the ideas of a discrete time branching process with random environments and a continuous time non-homogeneous Markov branching process. The extinction problem is considered and necessary and sufficient conditions for extinction are determined. Also discussed are limit theorems for what corresponds to the supercritical case.


Author(s):  
Azam A. Imomov ◽  

The paper discusses the continuous-time Markov Branching Process allowing Immigration. We are considering a critical case for which the second moment of offspring law and the first moment of immigration law are possibly infinite. Assuming that the nonlinear parts of the appropriate generating functions are regularly varying in the sense of Karamata, we prove theorems on convergence of transition functions of the process to invariant measures. We deduce the speed rate of these convergence providing that slowly varying factors are with remainder


1980 ◽  
Vol 12 (1) ◽  
pp. 81-93 ◽  
Author(s):  
B. Klein ◽  
P. D. M. MacDonald

The multitype continuous-time Markov branching process has many biological applications where the environmental factors vary in a periodic manner. Circadian or diurnal rhythms in cell kinetics are an important example. It is shown that in the supercritical positively regular case the proportions of individuals of various types converge in probability to a non-random periodic vector, independent of the initial conditions, while the absolute numbers of individuals of various types converge in probability to that vector multiplied by a random variable whose distribution depends on the initial conditions. It is noted that the proofs are straightforward extensions of the well-known results for a constant environment.


1980 ◽  
Vol 12 (01) ◽  
pp. 81-93 ◽  
Author(s):  
B. Klein ◽  
P. D. M. MacDonald

The multitype continuous-time Markov branching process has many biological applications where the environmental factors vary in a periodic manner. Circadian or diurnal rhythms in cell kinetics are an important example. It is shown that in the supercritical positively regular case the proportions of individuals of various types converge in probability to a non-random periodic vector, independent of the initial conditions, while the absolute numbers of individuals of various types converge in probability to that vector multiplied by a random variable whose distribution depends on the initial conditions. It is noted that the proofs are straightforward extensions of the well-known results for a constant environment.


1976 ◽  
Vol 13 (02) ◽  
pp. 219-230 ◽  
Author(s):  
J. Gani ◽  
I. W. Saunders

This paper is concerned with the parity of a population of yeast cells, each of which may bud, not bud or die. Two multitype models are considered: a Galton-Watson process in discrete time, and its analogous birth-death process in continuous time. The mean number of cells with parity 0, 1, 2, … is obtained in both cases; some simple results are also derived for the second moments of the two processes.


2009 ◽  
Vol 46 (01) ◽  
pp. 296-307 ◽  
Author(s):  
Dominik Heinzmann

In this paper, a distributional approximation to the time to extinction in a subcritical continuous-time Markov branching process is derived. A limit theorem for this distribution is established and the error in the approximation is quantified. The accuracy of the approximation is illustrated in an epidemiological example. Since Markov branching processes serve as approximations to nonlinear epidemic processes in the initial and final stages, our results can also be used to describe the time to extinction for such processes.


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