Birth–death process

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The birth–death process (or birth-and-death process) is a special case of continuous-time Markov process where the state transitions are of only two types: "births", which increase the state variable by one and "deaths", which decrease the state by one. It was introduced by William Feller.[1] The model's name comes from a common application, the use of such models to represent the current size of a population where the transitions are literal births and deaths. Birth–death processes have many applications in demography, queueing theory, performance engineering, epidemiology, biology and other areas. They may be used, for example, to study the evolution of bacteria, the number of people with a disease within a population, or the number of customers in line at the supermarket.

Definition

When a birth occurs, the process goes from state n to n + 1. When a death occurs, the process goes from state n to state n − 1. The process is specified by positive birth rates {λi}i=0 and positive death rates {μi}i=1. The number of individuals in the process at time t is denoted by X(t). The process has the Markov property and Pi,j(t)=P{X(t+s)=j|X(s)=i} describes how X(t) changes through time. For small t>0, the function Pi,j(t) is assumed to satisfy the following properties:

Pi,i+1(t)=λit+o(t),i0,
Pi,i1(t)=μit+o(t),i1,
Pi,i(t)=1(λi+μi)t+o(t),i1.

This process is represented by the following figure with the states of the process (i.e. the number of individuals in the population) depicted by the circles, and transitions between states indicated by the arrows. State diagram of a birth-death process

Recurrence and transience

For recurrence and transience in Markov processes see Section 5.3 from Markov chain.

Conditions for recurrence and transience

Conditions for recurrence and transience were established by Samuel Karlin and James McGregor.[2]

A birth-and-death process is recurrent if and only if
i=1n=1iμnλn=.
A birth-and-death process is ergodic if and only if
i=1n=1iμnλn=andi=1n=1iλn1μn<.
A birth-and-death process is null-recurrent if and only if
i=1n=1iμnλn=andi=1n=1iλn1μn=.

By using Extended Bertrand's test (see Section 4.1.4 from Ratio test) the conditions for recurrence, transience, ergodicity and null-recurrence can be derived in a more explicit form.[3] For integer K1, let ln(K)(x) denote the Kth iterate of natural logarithm, i.e. ln(1)(x)=ln(x) and for any 2kK, ln(k)(x)=ln(k1)(ln(x)). Then, the conditions for recurrence and transience of a birth-and-death process are as follows.

The birth-and-death process is transient if there exist c>1, K1 and n0 such that for all n>n0
λnμn1+1n+1nk=1K11j=1kln(j)(n)+cnj=1Kln(j)(n),

where the empty sum for K=1 is assumed to be 0.

The birth-and-death process is recurrent if there exist K1 and n0 such that for all n>n0
λnμn1+1n+1nk=1K1j=1kln(j)(n).

Wider classes of birth-and-death processes, for which the conditions for recurrence and transience can be established, can be found in.[4]

Application

Consider one-dimensional random walk St,t=0,1,, that is defined as follows. Let S0=1, and St=St1+et,t1, where et takes values ±1, and the distribution of St is defined by the following conditions:

P{St+1=St+1|St>0}=12+αStSt,P{St+1=St1|St>0}=12αStSt,P{St+1=1|St=0}=1,

where αn satisfy the condition 0<αn<min{C,n/2},C>0. The random walk described here is a discrete time analogue of the birth-and-death process (see Markov chain) with the birth rates

λn=12+αnn,

and the death rates

μn=12αnn.

So, recurrence or transience of the random walk is associated with recurrence or transience of the birth-and-death process.[3]

The random walk is transient if there exist c>1, K1 and n0 such that for all n>n0
αn14(1+k=1K1j=1k1ln(j)(n)+cj=1K1ln(j)(n)),

where the empty sum for K=1 is assumed to be zero.

The random walk is recurrent if there exist K1 and n0 such that for all n>n0
αn14(1+k=1Kj=1k1ln(j)(n)).

Stationary solution

If a birth-and-death process is ergodic, then there exists steady-state probabilities πk=limtpk(t), where pk(t) is the probability that the birth-and-death process is in state k at time t. The limit exists, independent of the initial values pk(0), and is calculated by the relations:

πk=π0i=1kλi1μi,k=1,2,,
π0=11+k=1i=1kλi1μi.

These limiting probabilities are obtained from the infinite system of differential equations for pk(t):

p0(t)=μ1p1(t)λ0p0(t)
pk(t)=λk1pk1(t)+μk+1pk+1(t)(λk+μk)pk(t),k=1,2,,

and the initial condition k=0pk(t)=1. In turn, the last system of differential equations is derived from the system of difference equations that describes the dynamic of the system in a small time Δt. During this small time Δt only three types of transitions are considered as one death, or one birth, or no birth nor death. The probability of the first two of these transitions has the order of Δt. Other transitions during this small interval Δt such as more than one birth, or more than one death, or at least one birth and at least one death have the probabilities that are of smaller order than Δt, and hence are negligible in derivations. If the system is in state k, then the probability of birth during an interval Δt is λkΔt+o(Δt), the probability of death is μkΔt+o(Δt), and the probability of no birth and no death is 1λkΔtμkΔt+o(Δt). For a population process, "birth" is the transition towards increasing the population size by 1 while "death" is the transition towards decreasing the population size by 1.

Examples of birth-death processes

A pure birth process is a birth–death process where μi=0 for all i0. A pure death process is a birth–death process where λi=0 for all i0. M/M/1 model and M/M/c model, both used in queueing theory, are birth–death processes used to describe customers in an infinite queue.

Use in phylodynamics

Birth–death processes are used in phylodynamics as a prior distribution for phylogenies, i.e. a binary tree in which birth events correspond to branches of the tree and death events correspond to leaf nodes.[5] Notably, they are used in viral phylodynamics[6] to understand the transmission process and how the number of people infected changes through time.[7] The use of generalized birth-death processes in phylodynamics has stimulated investigations into the degree to which the rates of birth and death can be identified from data.[8] While the model is unidentifiable in general, the subset of models that are typically used are identifiable.[9]

Use in queueing theory

In queueing theory the birth–death process is the most fundamental example of a queueing model, the M/M/C/K//FIFO (in complete Kendall's notation) queue. This is a queue with Poisson arrivals, drawn from an infinite population, and C servers with exponentially distributed service times with K places in the queue. Despite the assumption of an infinite population this model is a good model for various telecommunication systems.

M/M/1 queue

The M/M/1 is a single server queue with an infinite buffer size. In a non-random environment the birth–death process in queueing models tend to be long-term averages, so the average rate of arrival is given as λ and the average service time as 1/μ. The birth and death process is an M/M/1 queue when,

λi=λ and μi=μ for all i.

The differential equations for the probability that the system is in state k at time t are

p0(t)=μp1(t)λp0(t),
pk(t)=λpk1(t)+μpk+1(t)(λ+μ)pk(t)for k=1,2,

Pure birth process associated with an M/M/1 queue

Pure birth process with λkλ is a particular case of the M/M/1 queueing process. We have the following system of differential equations:

p0(t)=λp0(t),
pk(t)=λpk1(t)λpk(t)for k=1,2,

Under the initial condition p0(0)=1 and pk(0)=0,k=1,2,, the solution of the system is

pk(t)=(λt)kk!eλt.

That is, a (homogeneous) Poisson process is a pure birth process.

M/M/c queue

The M/M/C is a multi-server queue with C servers and an infinite buffer. It characterizes by the following birth and death parameters:

μi=iμ for iC1,

and

μi=Cμ for iC,

with

λi=λ for all i.

The system of differential equations in this case has the form:

p0(t)=μp1(t)λp0(t),
pk(t)=λpk1(t)+(k+1)μpk+1(t)(λ+kμ)pk(t)for k=1,2,,C1,
pk(t)=λpk1(t)+Cμpk+1(t)(λ+Cμ)pk(t)for kC.

Pure death process associated with an M/M/C queue

Pure death process with μk=kμ is a particular case of the M/M/C queueing process. We have the following system of differential equations:

pC(t)=CμpC(t),
pk(t)=(k+1)μpk+1(t)kμpk(t)for k=0,1,,C1.

Under the initial condition pC(0)=1 and pk(0)=0,k=0,1,,C1, we obtain the solution

pk(t)=(Ck)ekμt(1eμt)Ck,

that presents the version of binomial distribution depending on time parameter t (see Binomial process).

M/M/1/K queue

The M/M/1/K queue is a single server queue with a buffer of size K. This queue has applications in telecommunications, as well as in biology when a population has a capacity limit. In telecommunication we again use the parameters from the M/M/1 queue with,

λi=λ for 0i<K,
λi=0 for iK,
μi=μ for 1iK.

In biology, particularly the growth of bacteria, when the population is zero there is no ability to grow so,

λ0=0.

Additionally if the capacity represents a limit where the individual dies from over population,

μK=0.

The differential equations for the probability that the system is in state k at time t are

p0(t)=μp1(t)λp0(t),
pk(t)=λpk1(t)+μpk+1(t)(λ+μ)pk(t) for kK1,
pK(t)=λpK1(t)(λ+μ)pK(t),
pk(t)=0 for k>K.

Equilibrium

A queue is said to be in equilibrium if the steady state probabilities πk=limtpk(t),k=0,1,, exist. The condition for the existence of these steady-state probabilities in the case of M/M/1 queue is ρ=λ/μ<1 and in the case of M/M/C queue is ρ=λ/(Cμ)<1. The parameter ρ is usually called load parameter or utilization parameter. Sometimes it is also called traffic intensity. Using the M/M/1 queue as an example, the steady state equations are

λπ0=μπ1,
(λ+μ)πk=λπk1+μπk+1.

This can be reduced to

λπk=μπk+1 for k0.

So, taking into account that π0+π1+=1, we obtain

πk=(1ρ)ρk.

Bilateral birth-and-death process

Bilateral birth-and-death process is defined similarly to that standard one with the only difference that the birth and death rates λi and μi are defined for the values of index parameter i=0,±1,±2,.[10] Following this, a bilateral birth-and-death process is recurrent if and only if

i=1n=1iμnλn=andi=1n=1iλnμn=.

The notions of ergodicity and null-recurrence are defined similarly by extending the corresponding notions of the standard birth-and-death process.

See also

Notes

  1. Feller, William (1939). "Die Grundlagen der Volterraschen Theorie des Kampfes ums Dasein in wahrscheinlichkeitstheoretischer Behandlung". Acta Biotheoretica. 5 (1): 11–40. doi:10.1007/BF01602932.
  2. Karlin, Samuel; McGregor, James (1957). "The classification of birth and death processes" (PDF). Transactions of the American Mathematical Society. 86 (2): 366–400. doi:10.1090/S0002-9947-1957-0094854-8.
  3. 3.0 3.1 Abramov, Vyacheslav M. (2020). "Extension of the Bertrand–De Morgan test and its application". The American Mathematical Monthly. 127 (5): 444–448. arXiv:1901.05843. doi:10.1080/00029890.2020.1722551. S2CID 199552015.
  4. Abramov, Vyacheslav M. (2022). "Necessary and sufficient conditions for the convergence of positive series" (PDF). Journal of Classical Analysis. 19 (2): 117–125. arXiv:2104.01702. doi:10.7153/jca-2022-19-09. S2CID 233025219.
  5. Stadler T (December 2010). "Sampling-through-time in birth-death trees". Journal of Theoretical Biology. 267 (3): 396–404. Bibcode:2010JThBi.267..396S. doi:10.1016/j.jtbi.2010.09.010. PMID 20851708.
  6. Kühnert D, Wu CH, Drummond AJ (December 2011). "Phylogenetic and epidemic modeling of rapidly evolving infectious diseases". Infection, Genetics and Evolution. 11 (8): 1825–41. doi:10.1016/j.meegid.2011.08.005. PMC 7106223. PMID 21906695.
  7. Zarebski AE, du Plessis L, Parag KV, Pybus OG (February 2022). "A computationally tractable birth-death model that combines phylogenetic and epidemiological data". PLOS Computational Biology. 18 (2): e1009805. Bibcode:2022PLSCB..18E9805Z. doi:10.1371/journal.pcbi.1009805. PMC 8903285. PMID 35148311.
  8. Louca S, Pennell MW (April 2020). "Extant timetrees are consistent with a myriad of diversification histories" (PDF). Nature. 508 (7804): 502–505. Bibcode:2020Natur.580..502L. doi:10.1038/s41586-020-2176-1. PMID 32322065. S2CID 215775763.
  9. Legried B, Terhorst (August 2022). "A class of identifiable phylogenetic birth–death models". PNAS. 119 (35): e2119513119. Bibcode:2022PNAS..11919513L. doi:10.1073/pnas.2119513119. PMC 9436344. PMID 35994663.
  10. Pruitt, William E. (1963). "Bilateral birth and death processes" (PDF). Transactions of the American Mathematical Society. 107 (3): 508–525. doi:10.1090/S0002-9947-1963-0150858-0.

References

  • Latouche, G.; Ramaswami, V. (1999). "Quasi-Birth-and-Death Processes". Introduction to Matrix Analytic Methods in Stochastic Modelling (1st ed.). ASA SIAM. ISBN 0-89871-425-7.
  • Nowak, M. A. (2006). Evolutionary Dynamics: Exploring the Equations of Life. Harvard University Press. ISBN 0-674-02338-2.
  • Virtamo, J. "Birth-death processes" (PDF). 38.3143 Queueing Theory. Retrieved 2 December 2019.