Search

Pollen is generally dispersed over short distances, which promotes population genetic structure across continuous two-dimensional space. Quantitative genetic variance in flowering time structures mating pools in the temporal dimension, at least with respect to the phenology loci. We asked if these two phenomena, isolation by distance (IBD) and isolation by phenology (IBP), synergistically promote genetic structure. We constructed an individual-based model that tracked genotype frequencies at flowering time and neutral loci across a uniform landscape, over multiple generations, under four mating schemes: panmixia, IBD only, IBP only, and IBP × IBD. IBD × IBP divided the population into spatial clusters of early-, mid-, and late-flowering genotypes and strongly increased its quantitative genetic variance. Flowering time did not cluster under IBP, but its genetic variance increased moderately. IBD induced mild spatial structure in a nonassortative reference trait but did not change its variance. Importantly, the spatial correlation of genotypes at neutral loci was twice as strong under IBD × IBP compared with IBD alone. IBD × IBP also drew neutral loci into gametic disequilibrium with flowering time loci, structuring them temporally. Temporal and spatial mating pool structure promotes local differentiation. This trend would facilitate adaptation on small spatial scales., (© 2019 The Authors. New Phytologist © 2019 New Phytologist Trust.)

Coexpression of genes in plant sporophytes and gametophytes allows correlated gametic and sporophytic selection. Theory predicts that, under outcrossing, an allele conferring greater pollen competitive ability should fix within a population unless antagonistic pleiotropy with the sporophyte stage is strong. However, under strong selfing, pollen competitiveness is immaterial as superior and inferior competitors are deposited on opposite stigmas, producing assortative competition. Because many plant species have mixed-mating systems, selfing should be critical in the spread and maintenance of pollen-expressed genes affecting competitiveness. We present two one-locus, two-allele population genetic models for the evolution of a locus controlling pleiotropic antagonism between pollen competitiveness and diploid fitness. Analytical solutions provide minimum and maximum selfing rates allowing invasion of alleles with greater diploid and haploid fitness, respectively. Further, polymorphism is only maintained when diploid selection is recessive. Fixation of the allele conferring greater pollen competitiveness may be prevented, even with weak sporophytic counterselection, with sufficiently high selfing. Finally, selfing expands and limits the range of haploid-diploid selection coefficients allowing polymorphism, depending on dominance and selfing mode., (© 2018 The Author(s). Evolution © 2018 The Society for the Study of Evolution.)