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Genetics. 1983 Mar; 103(3): 557–579.
PMCID: PMC1202040

Models of Evolution of Reproductive Isolation

Abstract

Mathematical models are presented for the evolution of postmating and premating reproductive isolation. In the case of postmating isolation it is assumed that hybrid sterility or inviability is caused by incompatibility of alleles at one or two loci, and evolution of reproductive isolation occurs by random fixation of different incompatibility alleles in different populations. Mutations are assumed to occur following either the stepwise mutation model or the infinite-allele model. Computer simulations by using Itô's stochastic differential equations have shown that in the model used the reproductive isolation mechanism evolves faster in small populations than in large populations when the mutation rate remains the same. In populations of a given size it evolves faster when the number of loci involved is large than when this is small. In general, however, evolution of isolation mechanisms is a very slow process, and it would take thousands to millions of generations if the mutation rate is of the order of 10-5 per generation. Since gene substitution occurs as a stochastic process, the time required for the establishment of reproductive isolation has a large variance. Although the average time of evolution of isolation mechanisms is very long, substitution of incompatibility genes in a population occurs rather quickly once it starts. The intrapopulational fertility or viability is always very high. In the model of premating isolation it is assumed that mating preference or compatibility is determined by male- and female-limited characters, each of which is controlled by a single locus with multiple alleles, and mating occurs only when the male and female characters are compatible with each other. Computer simulations have shown that the dynamics of evolution of premating isolation mechanism is very similar to that of postmating isolation mechanism, and the mean and variance of the time required for establishment of premating isolation are very large. Theoretical predictions obtained from the present study about the speed of evolution of reproductive isolation are consistent with empirical data available from vertebrate organisms.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • KIMURA M, CROW JF. THE NUMBER OF ALLELES THAT CAN BE MAINTAINED IN A FINITE POPULATION. Genetics. 1964 Apr;49:725–738. [PMC free article] [PubMed]
  • Li WH. Distribution of nucleotide differences between two randomly chosen cistrons in a finite population. Genetics. 1977 Feb;85(2):331–337. [PMC free article] [PubMed]
  • Templeton AR. The theory of speciation via the founder principle. Genetics. 1980 Apr;94(4):1011–1038. [PMC free article] [PubMed]
  • Wilson AC, Maxson LR, Sarich VM. Two types of molecular evolution. Evidence from studies of interspecific hybridization. Proc Natl Acad Sci U S A. 1974 Jul;71(7):2843–2847. [PMC free article] [PubMed]
  • Zouros E. The chromosomal basis of sexual isolation in two sibling species of Drosophila: D. arizonensis and D. mojavensis. Genetics. 1981 Mar-Apr;97(3-4):703–718. [PMC free article] [PubMed]

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