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Letter
Nature 444, 89-92 (2 November 2006) | doi:10.1038/nature05206; Received 2 July 2006; Accepted 6 September 2006
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Post-mating sexual selection increases lifetime fitness of polyandrous females in the wild
Diana O. Fisher1, Michael C. Double1, Simon P. Blomberg2, Michael D. Jennions1 & Andrew Cockburn1
- School of Botany and Zoology, and,
- Centre for Resource and Environmental Studies, Australian National University, Canberra, Australian Capital Territory 0200, Australia
Correspondence to: Diana O. Fisher1 Correspondence and requests for materials should be addressed to D.O.F. (Email: diana.fisher@anu.edu.au).
Abstract
Females often mate with several males before producing offspring1. Field studies of vertebrates suggest, and laboratory experiments on invertebrates confirm, that even when males provide no material benefits, polyandry can enhance offspring survival2, 3. This enhancement is widely attributed to genetic benefits that arise whenever paternity is biased towards males that sire more viable offspring1, 4, 5. Field studies suggest that post-mating sexual selection biases fertilization towards genetically more compatible males6, 7 and one controlled experiment has shown that, when females mate with close kin, polyandry reduces the relative number of inbred offspring8. Another potential genetic benefit of polyandry is that it increases offspring survival because males with more competitive ejaculates sire more viable offspring9. Surprisingly, however, there is no unequivocal evidence for this process10. Here, by experimentally assigning mates to females, we show that polyandry greatly increases offspring survival in the Australian marsupial Antechinus stuartii. DNA profiling shows that males that gain high paternity under sperm competition sire offspring that are more viable. This beneficial effect occurs in both the laboratory and the wild. Crucially, there are no confounding non-genetic maternal effects that could arise if polyandry increases female investment in a particular reproductive event10 because A. stuartii is effectively semelparous. Our results therefore show that polyandry improves female lifetime fitness in nature. The threefold increase in offspring survival is not negated by a decline in maternal lifespan and is too large to be offset by an equivalent decline in the reproductive performance of surviving offspring.
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