Limit Behavior of Decomposable Critical Branching Processes with Two Types of Particles

1983 ◽  
Vol 27 (2) ◽  
pp. 235-247 ◽  
Author(s):  
A. M. Zubkov
Keyword(s):  
Branching Processes ◽  
Limit Behavior

scholarly journals The Limit Behavior of Dual Markov Branching Processes

2008 ◽  
Vol 45 (1) ◽  
pp. 176-189 ◽  
Author(s):  
Yangrong Li ◽  
Anthony G. Pakes ◽  
Jia Li ◽  
Anhui Gu
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Limit Behavior ◽  
Positive Recurrence ◽  
Strong Ergodicity ◽  
Feller Property ◽  
Markov Branching Process ◽  
Invariant Distributions ◽  
Geometric Limit ◽  
Branching Property

A dual Markov branching process (DMBP) is by definition a Siegmund's predual of some Markov branching process (MBP). Such a process does exist and is uniquely determined by the so-called dual-branching property. Its q-matrix Q is derived and proved to be regular and monotone. Several equivalent definitions for a DMBP are given. The criteria for transience, positive recurrence, strong ergodicity, and the Feller property are established. The invariant distributions are given by a clear formulation with a geometric limit law.

scholarly journals The Limit Behavior of Dual Markov Branching Processes

2008 ◽  
Vol 45 (01) ◽  
pp. 176-189
Author(s):  
Yangrong Li ◽  
Anthony G. Pakes ◽  
Jia Li ◽  
Anhui Gu
Keyword(s):  
Branching Process ◽  
Branching Processes ◽  
Limit Behavior ◽  
Positive Recurrence ◽  
Strong Ergodicity ◽  
Feller Property ◽  
Markov Branching Process ◽  
Invariant Distributions ◽  
Geometric Limit ◽  
Branching Property

A dual Markov branching process (DMBP) is by definition a Siegmund's predual of some Markov branching process (MBP). Such a process does exist and is uniquely determined by the so-called dual-branching property. Its q-matrix Q is derived and proved to be regular and monotone. Several equivalent definitions for a DMBP are given. The criteria for transience, positive recurrence, strong ergodicity, and the Feller property are established. The invariant distributions are given by a clear formulation with a geometric limit law.

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.

Ultrastructure of myoepithelial cell in parotid gland

1988 ◽  
Vol 46 ◽  
pp. 342-343
Author(s):  
C. N. Sun
Keyword(s):  
Parotid Gland ◽  
Osmium Tetroxide ◽  
Individual Cell ◽  
Branching Processes ◽  
Muscle Cells ◽  
Myoepithelial Cells ◽  
Uranyl Acetate ◽  
Thin Sections ◽  
Gland Carcinoma ◽  
Parotid Gland Carcinoma

Myoepithelial cells have been observed in the prostate, harderian, apocrine, exocrine sweat and mammary glands. Such cells and their numerous branching processes form basket-like structures around the glandular acini. Their shapes are quite different from structures seen either in spindleshaped smooth muscle cells or skeletal muscle cells. These myoepithelial cells lie on the epithelial side of the basement membrane in the glands. This presentation describes the ultrastructure of such myoepithelial cells which have been found also in the parotid gland carcinoma from a 45-year old patient.Specimens were cut into small pieces about 1 mm3 and immediately fixed in 4 percent glutaraldehyde in phosphate buffer for two hours, then post-fixed in 1 percent buffered osmium tetroxide for 1 hour. After dehydration, tissues were embedded in Epon 812. Thin sections were stained with uranyl acetate and lead citrate. Ultrastructurally, the pattern of each individual cell showed wide variations.

Regenerative Sampling and Monotonic Branching Processes.

1986 ◽  
Author(s):  
Stephen D. Durham ◽  
Kai F. Yu
Keyword(s):  
Branching Processes

On calculating extinction probabilities for branching processes in random environments

1969 ◽  
Vol 6 (03) ◽  
pp. 478-492 ◽  
Author(s):  
William E. Wilkinson
Keyword(s):  
Generating Functions ◽  
Infinite Sequence ◽  
Branching Processes ◽  
Transition Probability ◽  
Transition Probability Matrix ◽  
Random Environments ◽  
Real Numbers ◽  
Discrete Time Markov Chain ◽  
Extinction Probabilities ◽  
Image Position

Consider a discrete time Markov chain {Zn } whose state space is the non-negative integers and whose transition probability matrix ║Pij ║ possesses the representation where {Pr }, r = 1,2,…, is a finite or denumerably infinite sequence of non-negative real numbers satisfying , and , is a corresponding sequence of probability generating functions. It is assumed that Z 0 = k, a finite positive integer.

scholarly journals Limit theorems for multi-type general branching processes with population dependence

2020 ◽  
Vol 52 (4) ◽  
pp. 1127-1163
Author(s):  
Jie Yen Fan ◽  
Kais Hamza ◽  
Peter Jagers ◽  
Fima C. Klebaner
Keyword(s):  
Carrying Capacity ◽  
Population Model ◽  
General Framework ◽  
Limit Theorems ◽  
Mating Systems ◽  
Law Of Large Numbers ◽  
Branching Processes ◽  
Special Section ◽  
Large Numbers ◽  
Type Population

AbstractA general multi-type population model is considered, where individuals live and reproduce according to their age and type, but also under the influence of the size and composition of the entire population. We describe the dynamics of the population as a measure-valued process and obtain its asymptotics as the population grows with the environmental carrying capacity. Thus, a deterministic approximation is given, in the form of a law of large numbers, as well as a central limit theorem. This general framework is then adapted to model sexual reproduction, with a special section on serial monogamic mating systems.

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