scholarly journals A note on the multitype measure branching process

1992 ◽  
Vol 24 (2) ◽  
pp. 496-498 ◽  
Author(s):  
Zeng-Hu Li
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Single Type ◽  
Type Model

The existence of a class of multitype measure branching processes is deduced from a single-type model introduced by Li [8], which extends the work of Gorostiza and Lopez-Mimbela [5] and shows that the study of a multitype process can sometimes be reduced to that of a single-type one.

scholarly journals A note on the multitype measure branching process

1992 ◽  
Vol 24 (02) ◽  
pp. 496-498 ◽  
Author(s):  
Zeng-Hu Li
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Single Type ◽  
Type Model

The existence of a class of multitype measure branching processes is deduced from a single-type model introduced by Li [8], which extends the work of Gorostiza and Lopez-Mimbela [5] and shows that the study of a multitype process can sometimes be reduced to that of a single-type one.

scholarly journals Coalescence in Subcritical Bellman-Harris Age-Dependent Branching Processes

2013 ◽  
Vol 50 (2) ◽  
pp. 576-591
Author(s):  
Jyy-I Hong
Keyword(s):  
Limit Distribution ◽  
Branching Process ◽  
Branching Processes ◽  
Simple Random Sampling ◽  
Single Type ◽  
Last Common Ancestor ◽  
Death Time ◽  
Age Dependent ◽  
Lines Of Descent ◽  
First Time

We consider a continuous-time, single-type, age-dependent Bellman-Harris branching process. We investigate the limit distribution of the point process A(t)={at,i: 1≤ i≤ Z(t)}, where at,i is the age of the ith individual alive at time t, 1≤ i≤ Z(t), and Z(t) is the population size of individuals alive at time t. Also, if Z(t)≥ k, k≥2, is a positive integer, we pick k individuals from those who are alive at time t by simple random sampling without replacement and trace their lines of descent backward in time until they meet for the first time. Let Dk(t) be the coalescence time (the death time of the last common ancestor) of these k random chosen individuals. We study the distribution of Dk(t) and its limit distribution as t→∞.

Coalescence in Subcritical Bellman-Harris Age-Dependent Branching Processes

2013 ◽  
Vol 50 (02) ◽  
pp. 576-591 ◽  
Author(s):  
Jyy-I Hong
Keyword(s):  
Limit Distribution ◽  
Branching Process ◽  
Branching Processes ◽  
Simple Random Sampling ◽  
Single Type ◽  
Last Common Ancestor ◽  
Death Time ◽  
Age Dependent ◽  
Lines Of Descent ◽  
First Time

We consider a continuous-time, single-type, age-dependent Bellman-Harris branching process. We investigate the limit distribution of the point process A(t)={a t,i : 1≤ i≤ Z(t)}, where a t,i is the age of the ith individual alive at time t, 1≤ i≤ Z(t), and Z(t) is the population size of individuals alive at time t. Also, if Z(t)≥ k, k≥2, is a positive integer, we pick k individuals from those who are alive at time t by simple random sampling without replacement and trace their lines of descent backward in time until they meet for the first time. Let D k(t) be the coalescence time (the death time of the last common ancestor) of these k random chosen individuals. We study the distribution of D k(t) and its limit distribution as t→∞.

scholarly journals A Host-Parasite Model for a Two-Type Cell Population

2013 ◽  
Vol 45 (03) ◽  
pp. 719-741 ◽  
Author(s):  
Gerold Alsmeyer ◽  
Sören Gröttrup
Keyword(s):  
B Cell ◽  
Random Environment ◽  
Branching Process ◽  
Relative Proportion ◽  
Single Type ◽  
Type Model ◽  
Daughter Cells ◽  
A Cell ◽  
Host Parasite ◽  
A And B Cells

We consider a host-parasite model for a population of cells that can be of two types, A or B, and exhibits unilateral reproduction: while a B-cell always splits into two cells of the same type, the two daughter cells of an A-cell can be of any type. The random mechanism that describes how parasites within a cell multiply and are then shared into the daughter cells is allowed to depend on the hosting mother cell as well as its daughter cells. Focusing on the subpopulation of A-cells and its parasites, our model differs from the single-type model recently studied by Bansaye (2008) in that the sharing mechanism may be biased towards one of the two types. Our main results are concerned with the nonextinctive case and provide information on the behavior, as n → ∞, of the number of A-parasites in generation n and the relative proportion of A- and B-cells in this generation which host a given number of parasites. As in Bansaye (2008), proofs will make use of a so-called random cell line which, when conditioned to be of type A, behaves like a branching process in a random environment.

scholarly journals A Host-Parasite Model for a Two-Type Cell Population

2013 ◽  
Vol 45 (3) ◽  
pp. 719-741
Author(s):  
Gerold Alsmeyer ◽  
Sören Gröttrup
Keyword(s):  
B Cell ◽  
Random Environment ◽  
Branching Process ◽  
Relative Proportion ◽  
Single Type ◽  
Type Model ◽  
Daughter Cells ◽  
A Cell ◽  
Host Parasite ◽  
A And B Cells

We consider a host-parasite model for a population of cells that can be of two types, A or B, and exhibits unilateral reproduction: while a B-cell always splits into two cells of the same type, the two daughter cells of an A-cell can be of any type. The random mechanism that describes how parasites within a cell multiply and are then shared into the daughter cells is allowed to depend on the hosting mother cell as well as its daughter cells. Focusing on the subpopulation of A-cells and its parasites, our model differs from the single-type model recently studied by Bansaye (2008) in that the sharing mechanism may be biased towards one of the two types. Our main results are concerned with the nonextinctive case and provide information on the behavior, as n → ∞, of the number of A-parasites in generation n and the relative proportion of A- and B-cells in this generation which host a given number of parasites. As in Bansaye (2008), proofs will make use of a so-called random cell line which, when conditioned to be of type A, behaves like a branching process in a random environment.

Some Contributions to the Theory of Near-Critical Bisexual Branching Processes

2007 ◽  
Vol 44 (02) ◽  
pp. 492-505
Author(s):  
M. Molina ◽  
M. Mota ◽  
A. Ramos
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Sufficient Conditions ◽  
Positive Probability ◽  
Limit Laws ◽  
Bisexual Branching Processes ◽  
Probabilistic Evolution

We investigate the probabilistic evolution of a near-critical bisexual branching process with mating depending on the number of couples in the population. We determine sufficient conditions which guarantee either the almost sure extinction of such a process or its survival with positive probability. We also establish some limiting results concerning the sequences of couples, females, and males, suitably normalized. In particular, gamma, normal, and degenerate distributions are proved to be limit laws. The results also hold for bisexual Bienaymé–Galton–Watson processes, and can be adapted to other classes of near-critical bisexual branching processes.

scholarly journals Skeletal stochastic differential equations for superprocesses

2020 ◽  
Vol 57 (4) ◽  
pp. 1111-1134
Author(s):  
Dorottya Fekete ◽  
Joaquin Fontbona ◽  
Andreas E. Kyprianou
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Subcritical Case ◽  
Markov Branching Process ◽  
Continuous State ◽  
Common Framework ◽  
Infinite Line ◽  
Current Article ◽  
Lines Of Descent ◽  
Skeletal Representation

AbstractIt is well understood that a supercritical superprocess is equal in law to a discrete Markov branching process whose genealogy is dressed in a Poissonian way with immigration which initiates subcritical superprocesses. The Markov branching process corresponds to the genealogical description of prolific individuals, that is, individuals who produce eternal genealogical lines of descent, and is often referred to as the skeleton or backbone of the original superprocess. The Poissonian dressing along the skeleton may be considered to be the remaining non-prolific genealogical mass in the superprocess. Such skeletal decompositions are equally well understood for continuous-state branching processes (CSBP).In a previous article [16] we developed an SDE approach to study the skeletal representation of CSBPs, which provided a common framework for the skeletal decompositions of supercritical and (sub)critical CSBPs. It also helped us to understand how the skeleton thins down onto one infinite line of descent when conditioning on survival until larger and larger times, and eventually forever.Here our main motivation is to show the robustness of the SDE approach by expanding it to the spatial setting of superprocesses. The current article only considers supercritical superprocesses, leaving the subcritical case open.

Branching processes and functional differential equations determining steady-size distributions in cell populations

1995 ◽  
Vol 32 (01) ◽  
pp. 1-10
Author(s):  
Ziad Taib
Keyword(s):  
Differential Equation ◽  
Branching Process ◽  
Branching Processes ◽  
Functional Differential Equations ◽  
Cell Populations ◽  
Size Distributions ◽  
Multitype Branching Process ◽  
Functional Differential ◽  
Intuitive Interpretation ◽  
Infinite Sum

The functional differential equation y′(x) = ay(λx) + by(x) arises in many different situations. The purpose of this note is to show how it arises in some multitype branching process cell population models. We also show how its solution can be given an intuitive interpretation as the probability density function of an infinite sum of independent but not identically distributed random variables.

Continuity for multi-type branching processes with varying environments

1999 ◽  
Vol 36 (01) ◽  
pp. 139-145 ◽  
Author(s):  
Owen Dafydd Jones
Keyword(s):  
Linear Combination ◽  
Branching Process ◽  
Branching Processes ◽  
Random Variables ◽  
Main Tool ◽  
Concentration Function ◽  
Independent Random Variables ◽  
Varying Environments

Conditions are derived for the components of the normed limit of a multi-type branching process with varying environments, to be continuous on (0, ∞). The main tool is an inequality for the concentration function of sums of independent random variables, due originally to Petrov. Using this, we show that if there is a discontinuity present, then a particular linear combination of the population types must converge to a non-random constant (Equation (1)). Ensuring this can not happen provides the desired continuity conditions.

On the convergence of the supercritical branching processes with immigration

1977 ◽  
Vol 14 (2) ◽  
pp. 387-390 ◽  
Author(s):  
Harry Cohn
Keyword(s):  
Distribution Function ◽  
Limit Distribution ◽  
Branching Process ◽  
Branching Processes ◽  
Sufficient Condition ◽  
Necessary And Sufficient Condition ◽  
Limit Distribution Function ◽  
Branching Process With Immigration ◽  
Necessary And Sufficient ◽  
Supercritical Branching Processes

It is shown for a supercritical branching process with immigration that if the log moment of the immigration distribution is infinite, then no sequence of positive constants {cn} exists such that {Xn/cn} converges in law to a proper limit distribution function F, except for the case F(0 +) = 1. Seneta's result [1] combined with the above-mentioned one imply that if 1 < m < ∞ then the finiteness of the log moment of the immigration distribution is a necessary and sufficient condition for the existence of some constants {cn} such that {Xn/cn} converges in law to a proper limit distribution function F, with F(0 +) < 1.

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