Cargando…
Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female
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 coevolu...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552684/ https://www.ncbi.nlm.nih.gov/pubmed/28798399 http://dx.doi.org/10.1038/s41598-017-08390-3 |
_version_ | 1783256493833846784 |
---|---|
author | Cordero-Rivera, Adolfo |
author_facet | Cordero-Rivera, Adolfo |
author_sort | Cordero-Rivera, Adolfo |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5552684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55526842017-08-14 Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female Cordero-Rivera, Adolfo Sci Rep Article 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. Nature Publishing Group UK 2017-08-10 /pmc/articles/PMC5552684/ /pubmed/28798399 http://dx.doi.org/10.1038/s41598-017-08390-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cordero-Rivera, Adolfo Sexual conflict and the evolution of genitalia: male damselflies remove more sperm when mating with a heterospecific female |
title | 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_short | 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 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552684/ https://www.ncbi.nlm.nih.gov/pubmed/28798399 http://dx.doi.org/10.1038/s41598-017-08390-3 |
work_keys_str_mv | AT corderoriveraadolfo sexualconflictandtheevolutionofgenitaliamaledamselfliesremovemorespermwhenmatingwithaheterospecificfemale |