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)).