Background: Strict genetic monogamy leads to sexual harmony because any tra
it that decreases the fitness of one sex also decreases the fitness of the
other. Any deviation from monogamy increases the potential for sexual confl
ict. Conflict is further enhanced by sperm competition, and given the ubiqu
ity of this phenomenon, sexual conflict is rife. In support of theory, expe
rimentally enforced monogamy leads to the evolution of sexual benevolence.
In contrast, with multiple mating, males evolve traits causing massive fema
le fitness reductions when female evolution is restrained. Theory also pred
icts increased investment in spermatogenesis when sperm competition risk is
high. While this supposition has correlational supper?, cause and effect h
as yet to be firmly established.
Results: By enforcing monogamy or polyandry in yellow-dung-fly lines, we ha
ve shown experimentally that males from polyandrous treatments evolved larg
er testes. Furthermore, females from this treatment evolved larger accessor
y sex glands. These glands produce a spermicidal secretion, so larger gland
s could increase female ability to influence paternity. Using molecular tec
hniques, we have shown that, consistent with this idea, males' success as s
econd mates is reduced in females from the polyandrous treatment. Neverthel
ess, males from polyandrous lines achieve higher paternity during sperm com
petition, and this finding further supports the testis evolution patterns.
Conclusions: These results provide direct experimental support for macroevo
lutionary patterns of testis size evolution. Furthermore, we have shown tha
t sperm competition selects for traits likely to be important in sexual con
flicts over paternity, a result only previously demonstrated in Drosophila
melanogaster.