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SEXUAL CONFLICT AND INTERACTING PHENOTYPES: A QUANTITATIVE GENETIC ANALYSIS OF FECUNDITY AND COPULA DURATION IN DROSOPHILA MELANOGASTER
Authors:Dominic A Edward  Jocelyn Poissant  Alastair J Wilson  Tracey Chapman
Institution:1. School of Biological Sciences, University of East Anglia, Norwich Research Park, , Norwich, Norfolk NR4 7TJ United Kingdom;2. Mammalian Behaviour & Evolution, Institute of Integrative Biology, University of Liverpool, Leahurst Campus, , Neston CH64 7TE United Kingdom;3. Department of Animal and Plant Sciences, University of Sheffield, , Sheffield S10 2TN United Kingdom;4. Centre for Ecology and Conservation, University of Exeter, Penryn Campus, , Cornwall TR10 9EZ United Kingdom
Abstract:Many reproductive traits that have evolved under sexual conflict may be influenced by both sexes. Investigation of the genetic architecture of such traits can yield important insight into their evolution, but this entails that the heritable component of variation is estimated for males and females—as an interacting phenotype. We address the lack of research in this area through an investigation of egg production and copula duration in the fruit fly, Drosophila melanogaster. Despite egg production rate being determined by both sexes, which may cause sexual conflict, an assessment of this trait as an interacting phenotype is lacking. It is currently unclear whether copula duration is determined by males and/or females. We found significant female, but not male, genetic variance for egg production rate that may indicate reduced potential for ongoing sexually antagonistic coevolution. In contrast, copula duration was determined by significant genetic variance in both sexes. We also identified genetic variation in egg retention among virgin females. Although previously identified in wild populations, it is unclear why this should be present in a laboratory stock. This study provides a novel insight into the shared genetic architecture of reproductive traits that are the subject of sexual conflict.
Keywords:Heritability  mating systems  sexually antagonistic coevolution  sexual selection
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