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Paternity sharing in insects with female competition for nuptial gifts

Male parental investment is expected to be associated with high confidence of paternity. Studies of species with exclusive male parental care have provided support for this hypothesis because mating typically co‐occurs with each oviposition, allowing control over paternity and the allocation of care...

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Autores principales: Browne, Jessica H., Gwynne, Darryl T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618826/
https://www.ncbi.nlm.nih.gov/pubmed/36329813
http://dx.doi.org/10.1002/ece3.9463
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author Browne, Jessica H.
Gwynne, Darryl T.
author_facet Browne, Jessica H.
Gwynne, Darryl T.
author_sort Browne, Jessica H.
collection PubMed
description Male parental investment is expected to be associated with high confidence of paternity. Studies of species with exclusive male parental care have provided support for this hypothesis because mating typically co‐occurs with each oviposition, allowing control over paternity and the allocation of care. However, in systems where males invest by feeding mates (typically arthropods), mating (and thus the investment) is separated from egg‐laying, resulting in less control over insemination, as male ejaculates compete with rival sperm stored by females, and a greater risk of investing in unrelated offspring (cuckoldry). As strong selection on males to increase paternity would compromise the fitness of all a female's other mates that make costly nutrient contributions, paternity sharing (males not excluded from siring offspring) is an expected outcome of sperm competition. Using wild‐caught females in an orthopteran and a dipteran species, in which sexually selected, ornamented females compete for male nuptial food gifts needed for successful reproduction, we examined paternity patterns and compared them with findings in other insects. We used microsatellite analysis of offspring (lifetime reproduction in the orthopteran) and stored sperm from wild‐caught females in both study species. As predicted, there was evidence of shared paternity as few males failed to sire offspring. Further support for paternity sharing is the lack of last‐male sperm precedence in our study species. Although paternity was not equal among sires, our estimates of paternity bias were similar to other insects with valuable nuptial gifts and contrasted with the finding that males are frequently excluded from siring offspring in species where males supply little more than sperm. This suggests paternity bias may be reduced in nuptial‐gift systems and may help facilitate the evolution of these paternal investments.
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spelling pubmed-96188262022-11-02 Paternity sharing in insects with female competition for nuptial gifts Browne, Jessica H. Gwynne, Darryl T. Ecol Evol Research Articles Male parental investment is expected to be associated with high confidence of paternity. Studies of species with exclusive male parental care have provided support for this hypothesis because mating typically co‐occurs with each oviposition, allowing control over paternity and the allocation of care. However, in systems where males invest by feeding mates (typically arthropods), mating (and thus the investment) is separated from egg‐laying, resulting in less control over insemination, as male ejaculates compete with rival sperm stored by females, and a greater risk of investing in unrelated offspring (cuckoldry). As strong selection on males to increase paternity would compromise the fitness of all a female's other mates that make costly nutrient contributions, paternity sharing (males not excluded from siring offspring) is an expected outcome of sperm competition. Using wild‐caught females in an orthopteran and a dipteran species, in which sexually selected, ornamented females compete for male nuptial food gifts needed for successful reproduction, we examined paternity patterns and compared them with findings in other insects. We used microsatellite analysis of offspring (lifetime reproduction in the orthopteran) and stored sperm from wild‐caught females in both study species. As predicted, there was evidence of shared paternity as few males failed to sire offspring. Further support for paternity sharing is the lack of last‐male sperm precedence in our study species. Although paternity was not equal among sires, our estimates of paternity bias were similar to other insects with valuable nuptial gifts and contrasted with the finding that males are frequently excluded from siring offspring in species where males supply little more than sperm. This suggests paternity bias may be reduced in nuptial‐gift systems and may help facilitate the evolution of these paternal investments. John Wiley and Sons Inc. 2022-10-30 /pmc/articles/PMC9618826/ /pubmed/36329813 http://dx.doi.org/10.1002/ece3.9463 Text en © 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Browne, Jessica H.
Gwynne, Darryl T.
Paternity sharing in insects with female competition for nuptial gifts
title Paternity sharing in insects with female competition for nuptial gifts
title_full Paternity sharing in insects with female competition for nuptial gifts
title_fullStr Paternity sharing in insects with female competition for nuptial gifts
title_full_unstemmed Paternity sharing in insects with female competition for nuptial gifts
title_short Paternity sharing in insects with female competition for nuptial gifts
title_sort paternity sharing in insects with female competition for nuptial gifts
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618826/
https://www.ncbi.nlm.nih.gov/pubmed/36329813
http://dx.doi.org/10.1002/ece3.9463
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