Abstract
To better understand the sources of biological diversity in nature, we need information on the mechanisms underlying population divergence. Biological systems with patterns of naturally occurring adaptive variation among populations can provide insight into the genetic architecture of diverging traits and the influence of genetic constraints on responses to selection. Using a system of reproductive character displacement in the North American mushroom-feeding fly Drosophila subquinaria, we assessed patterns of genetic (co)variance among a suite of chemical signaling traits and divergence in this pattern among populations. D. subquinaria exhibits stronger reproductive isolation against the closely related Drosophila recens in sympatry, where both female mating preferences and male chemical signaling traits have diverged from the ancestral allopatric populations. We collected three wild populations from each region and, in the lab, characterized the phenotypic divergence in these traits, as well as the additive genetic (co)variance structure (G-matrix), via replicate breeding designs. We found divergence between allopatric and sympatric D. subquinaria in the shape and size of the G-matrix, and that the leading axis of genetic variance (gmax) had changed in sympatry to come into alignment with the primary axis of phenotypic divergence between the sympatric and allopatric regions.
Published Version
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