We derive the asymptotic behavior of the total, active, and inactive branch lengths of the seed bank coalescent when the initial sample size grows to infinity. These random variables have important applications for populations evolving under some seed bank effects, such as plants and bacteria, and for some cases of structured populations like metapopulations. The proof relies on the analysis of the tree at a stopping time corresponding to the first time a deactivated lineage is reactivated. We also give conditional sampling formulas for the random partition, and we study the system at the time of the first reactivation of a lineage. All these results provide a good picture of the different regimes and behaviors of the block-counting process of the seed bank coalescent.

The coalescent was introduced by Kingman (1982a), (1982b) and Tajima (1983) as a continuous-time Markov chain model describing the genealogical relationship among sampled genes from a panmictic population of a species. The random mating in a population is a strict condition and the genealogical structure of the population has a strong influence on the genetic variability and the evolution of the species. In this paper, starting from a discrete-time Markov chain model, we show the weak convergence to a continuous-time Markov chain, called the structured coalescent model, describing the genealogy of the sampled genes from whole population by means of passing the limit of the population size. Herbots (1997) proved the weak convergence to the structured coalescent on the condition of conservative migration and Wright–Fisher-type reproduction. We will give the proof on the condition of general migration rates and exchangeable reproduction.

We study the ancestral process of a sample from a subdivided population with stochastically varying subpopulation sizes. The sizes of the subpopulations change very rapidly (almost every generation) with respect to the coalescent time scale. For haploid populations of size N, one coalescence time unit corresponds to N generations. Coalescence and migration events occur on the same time scale. We show that, when the total population size tends to infinity, the structured coalescent is obtained, thus confirming the robustness of the coalescent. Many population structure models have been shown to converge to the structured coalescent (see Herbots (1997), Hudson (1998), Nordborg (2001), Nordborg and Krone (2002), and Notohara (1990)).

The structured coalescent is a continuous-time Markov chain which describes the genealogy of a sample of homologous genes from a subdivided population. Assuming this model, some results are proved relating to the genealogy of a pair of genes and the extent of subpopulation differentiation, which are valid under certain graph-theoretic symmetry and regularity conditions on the structure of the population. We first review and extend earlier results stating conditions under which the mean time since the most recent common ancestor of a pair of genes from any single subpopulation is independent of the migration rate and equal to that of two genes from an unstructured population of the same total size. Assuming the infinite alleles model of neutral mutation with a small mutation rate, we then prove a simple relationship between the migration rate and the value of Wright's coefficient FST for a pair of neighbouring subpopulations, which does not depend on the precise structure of the population provided that this is sufficiently symmetric.

In this paper, we present the distribution of the coalescence time of two DNA sequences (or genes) subject to symmetric migration between two islands, and conditional on the observed number of segregating sites in the sequences. The distribution for the segregating-site pattern is also obtained. Some surprising results emerge when both genes are initially on the same island. First, the post-data mean coalescence time is shown to be dependent on the migration parameter, as opposed to the pre-data mean. Second, both the post-data density and expectation for the coalescence time are shown to converge, in the weak-migration limit, to the corresponding panmictic results, as opposed to the pre-data situation where there is convergence in the density but not in the expectation. Finally, it is shown that there is convergence in the weak-migration limit in the distribution of the number of segregating sites but not in the expectation and variance. Numerical and graphical results for samples of size greater than two are also presented.

The aim of this paper is to study genealogical processes in a geographically structured population with weak migration. The coalescence time for sampled genes from different colonies diverges to infinity as the migration rates among colonies are close to zero. We investigate the moment generating functions of the coalescence time, the number of segregating sites and the number of allele types in sampled genes when there is low migration. Employing a perturbation method, we obtain a system of recurrence relations for the approximate solutions of these moment generating functions and solve them in some cases.

By applying a perturbation method to the structured coalescent process in population genetics theory, we obtain the approximate solutions of the moment generating functions for the total coalescence time, the number of segregating sites among sampled DNA sequences and the number of allele types in a sample in the case of strong migration.