Stochastic viability in an island model with partial dispersal: Approximation by a diffusion process in the limit of a large number of islands
q-bio.PE
Submitted: 2023-11-01
Updated: 2023-11-01
Journal ref: Theor. Popul. Biol., 158 (2024), pp. 170-184
DOI: 10.1016/j.tpb.2024.06.003
License: http://creativecommons.org/licenses/by/4.0/
The gist: In this paper, we study a finite population undergoing discrete, nonoverlapping generations, that is structured into D demes, each containing N individuals of two possible types, A and B, whose
Terminology
Abstract
In this paper, we study a finite population undergoing discrete, nonoverlapping generations, that is structured into D demes, each containing N individuals of two possible types, A and B, whose viability coefficients, s A and s B, respectively, vary randomly from one generation to the next. We assume that the means, variances and covariance of the viability coefficients are inversely proportional to the number of demes D, while higher-order moments are negligible in comparison to 1/D. We use a discrete-time Markov chain with two time scales to model the evolutionary process, and we demonstrate that as the number of demes D approaches infinity, the accelerated Markov chain converges to a diffusion process for any deme size N at least 2. This diffusion process allows us to evaluate the fixation probability of type A following its introduction as a single mutant in a population that was fixed for type B. We explore the impact of increasing the variability in the viability coefficients on this fixation probability. At least when N is large enough, it is shown that increasing this variability for type B or decreasing it for type A leads to an increase in the fixation probability of a single A. The effect of the population-scaled variances, σ 2 A and σ 2 B, can even cancel the effects of the population-scaled means, μ A and μ B. We also show that the fixation probability of a single A increases as the deme-scaled migration rate increases. Moreover, this probability is higher for type A than for type B if the population-scaled geometric mean is higher for type A than for type B, which means that μ A-σ A 2/2>μ B-σ B 2/2.
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