Selection for Male Weapons Boosts Female Fecundity, Eliminating Sexual Conflict in the Bulb Mite.

Extreme differences between the sexes are usually explained by intense sexual selection on male weapons or ornaments. Sexually antagonistic genes, with a positive effect on male traits but a negative effect on female fitness, create a negative inter-sexual correlation for fitness (sexual conflict). However, such antagonism might not be apparent if sexually selected male traits are condition-dependent, and condition elevates female fitness. Here we reveal a surprising positive genetic correlation between male weaponry and female fecundity. Using mite lines that had previously been through 13 generations of selection on male weapons (fighting legs), we investigated correlated evolution in female fecundity. Females from lines under positive selection for weapons (up lines) evolved higher fecundity, despite evolving costly, thicker legs. This is likely because male mites have condition-dependent weaponry that increases our ability to indirectly select on male condition. Alleles with positive effects on condition in both sexes could have generated this correlation because: the up lines evolved a higher proportion of fighters and there were positive correlations between weapon size and the male morph and sex ratios of the offspring. This positive inter-sexual genetic correlation should boost the evolution of male weapons and extreme sex differences.

Morph-specific artificial selection reveals a constraint on the evolution of polyphenisms.

Theory predicts that the evolution of polyphenic variation is facilitated where morphs are genetically uncoupled and free to evolve towards their phenotypic optima. However, the assumption that developmentally plastic morphs can evolve independently has not been tested directly. Using morph-specific artificial selection, we investigated correlated evolution between the sexes and male morphs of the bulb mite Rhizoglyphus echinopus Large 'fighter' males have a thick and sharply terminating pair of legs used to kill rival males, while small 'scrambler' males have unmodified legs, and search for unguarded females, avoiding fights. We selected on the relative leg width of only the fighter male morph, tracked the evolutionary responses in fighters and the correlated evolutionary responses in scramblers and females that were untouched by direct selection. Fighters diverged in relative leg thickness after six generations; assaying scramblers and females at the ninth generation we observed correlated responses in relative leg width in both. Our results represent strong evidence for the evolution of intraspecific phenotypic diversity despite correlated evolution between morphs and sexes, challenging the idea that male morphs are genetically uncoupled and free to independently respond to selection. We therefore question the perceived necessity for genetic independence in traits with extreme phenotypic plasticity.