The effect of the recombination rate between adaptive loci on the capacity of a population to expand its range

Abstract

Previous theoretical work on range expansions over heterogeneous environments showed that there is a critical environmental gradient where range expansion stops. For populations with freely recombining loci underlying the trait under selection (hereafter, “adaptive loci”), the critical gradient in one-dimensional habitats depends on the fitness cost of dispersal and the strength of selection relative to genetic drift. Here, we extend the previous work in two directions and ask, What is the role of the recombination rate between the adaptive loci during range expansions? And what effect does the ability of selfing as opposed to obligate outcrossing have on range expansions? To answer these questions, we use computer simulations. We demonstrate that while reduced recombination rates between adaptive loci slow down range expansions as a result of poor purging of locally deleterious alleles at the expansion front, they may also allow a species to occupy a greater range. In addition, we find that the allowance of selfing may improve the ability of populations to expand their ranges, for example, because selfing among potentially rare high-fitness individuals facilitates the establishment and maintenance of locally well-adapted genotypes. We conclude that during range expansions there is a trade-off between positive and negative effects of recombination within and between individuals.