Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female

Abstract In Calopteryx damselflies, males remove rivals’ sperm stored by the female, thereby reducing sperm competition. This behaviour may create a sexual conflict, because females could lose the sperm stored in the spermatheca, used for long-term storage. Comparative evidence suggested antagonisti...

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Main Author: Adolfo Cordero-Rivera
Format: Article
Language:English
Published: Nature Publishing Group 2017-08-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-08390-3
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spelling doaj-a4488752158e4adf833e785133db3e4a2020-12-08T00:36:03ZengNature Publishing GroupScientific Reports2045-23222017-08-01711810.1038/s41598-017-08390-3Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific femaleAdolfo Cordero-Rivera0ECOEVO Lab, Escola de Enxeñaría Forestal, Universidade de Vigo, Campus UniversitarioAbstract In Calopteryx damselflies, males remove rivals’ sperm stored by the female, thereby reducing sperm competition. This behaviour may create a sexual conflict, because females could lose the sperm stored in the spermatheca, used for long-term storage. Comparative evidence suggested antagonistic coevolution between sexes, which might prompt the evolution of narrow spermathecal ducts, or longer spermathecae, hindering sperm removal. Calopteryx haemorrhoidalis and C. splendens coexist and sometimes hybridize. Therefore, here I predicted that if females coevolve with conspecific males, heterospecific males should have an advantage when interspecific matings occur because females will show less resistance to them than to conspecific males. By hand-pairing females to males of both species, I found that in intraspecific and interspecific matings, sperm was almost completely removed from the bursa (97–100%), but only partially from the spermathecae, with more spermathecal removal in interspecific (63–71%) than intraspecific matings (14–33%). This suggests that heterospecific males are more efficient in sperm removal as predicted by a sexually-antagonistic coevolutionary scenario. Furthermore, in most cases, only the left spermatheca was emptied, suggesting that the evolution of more than one spermatheca might also be a female counter-adaptation to regain control over fertilization.https://doi.org/10.1038/s41598-017-08390-3
collection DOAJ
language English
format Article
sources DOAJ
author Adolfo Cordero-Rivera
spellingShingle Adolfo Cordero-Rivera
Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
Scientific Reports
author_facet Adolfo Cordero-Rivera
author_sort Adolfo Cordero-Rivera
title Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
title_short Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
title_full Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
title_fullStr Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
title_full_unstemmed Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
title_sort sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-08-01
description Abstract In Calopteryx damselflies, males remove rivals’ sperm stored by the female, thereby reducing sperm competition. This behaviour may create a sexual conflict, because females could lose the sperm stored in the spermatheca, used for long-term storage. Comparative evidence suggested antagonistic coevolution between sexes, which might prompt the evolution of narrow spermathecal ducts, or longer spermathecae, hindering sperm removal. Calopteryx haemorrhoidalis and C. splendens coexist and sometimes hybridize. Therefore, here I predicted that if females coevolve with conspecific males, heterospecific males should have an advantage when interspecific matings occur because females will show less resistance to them than to conspecific males. By hand-pairing females to males of both species, I found that in intraspecific and interspecific matings, sperm was almost completely removed from the bursa (97–100%), but only partially from the spermathecae, with more spermathecal removal in interspecific (63–71%) than intraspecific matings (14–33%). This suggests that heterospecific males are more efficient in sperm removal as predicted by a sexually-antagonistic coevolutionary scenario. Furthermore, in most cases, only the left spermatheca was emptied, suggesting that the evolution of more than one spermatheca might also be a female counter-adaptation to regain control over fertilization.
url https://doi.org/10.1038/s41598-017-08390-3
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