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Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus
Sperm competition risk and intensity can select for adaptations that increase male fertilisation success. Evolutionary responses are examined typically by generating increased strength of sexual selection via direct manipulation of female mating rates (by enforcing monandry or polyandry) or by alter...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910101/ https://www.ncbi.nlm.nih.gov/pubmed/27306351 http://dx.doi.org/10.1038/srep28153 |
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author | McNamara, Kathryn B. Robinson, Stephen P. Rosa, Márta E. Sloan, Nadia S. van Lieshout, Emile Simmons, Leigh W. |
author_facet | McNamara, Kathryn B. Robinson, Stephen P. Rosa, Márta E. Sloan, Nadia S. van Lieshout, Emile Simmons, Leigh W. |
author_sort | McNamara, Kathryn B. |
collection | PubMed |
description | Sperm competition risk and intensity can select for adaptations that increase male fertilisation success. Evolutionary responses are examined typically by generating increased strength of sexual selection via direct manipulation of female mating rates (by enforcing monandry or polyandry) or by alteration of adult sex ratios. Despite being a model species for sexual selection research, the effect of sexual selection intensity via adult sex-ratio manipulation on male investment strategies has not been investigated in the seed beetle, Callosobruchus maculatus. We imposed 32 generations of experimental evolution on 10 populations of beetles by manipulating adult sex ratio. Contrary to predictions, males evolving in male-biased populations did not increase their testes and accessory gland size. This absence of divergence in ejaculate investment was also reflected in the fact that males from male-biased populations were not more successful in either preventing females from remating, or in competing directly for fertilisations. These populations already demonstrate divergence in mating behaviour and immunity, suggesting sufficient generations have passed to allow divergence in physiological and behavioural traits. We propose several explanations for the absence of divergence in sperm competitiveness among our populations and the pitfalls of using sex ratio manipulation to assess evolutionary responses to sexual selection intensity. |
format | Online Article Text |
id | pubmed-4910101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49101012016-06-16 Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus McNamara, Kathryn B. Robinson, Stephen P. Rosa, Márta E. Sloan, Nadia S. van Lieshout, Emile Simmons, Leigh W. Sci Rep Article Sperm competition risk and intensity can select for adaptations that increase male fertilisation success. Evolutionary responses are examined typically by generating increased strength of sexual selection via direct manipulation of female mating rates (by enforcing monandry or polyandry) or by alteration of adult sex ratios. Despite being a model species for sexual selection research, the effect of sexual selection intensity via adult sex-ratio manipulation on male investment strategies has not been investigated in the seed beetle, Callosobruchus maculatus. We imposed 32 generations of experimental evolution on 10 populations of beetles by manipulating adult sex ratio. Contrary to predictions, males evolving in male-biased populations did not increase their testes and accessory gland size. This absence of divergence in ejaculate investment was also reflected in the fact that males from male-biased populations were not more successful in either preventing females from remating, or in competing directly for fertilisations. These populations already demonstrate divergence in mating behaviour and immunity, suggesting sufficient generations have passed to allow divergence in physiological and behavioural traits. We propose several explanations for the absence of divergence in sperm competitiveness among our populations and the pitfalls of using sex ratio manipulation to assess evolutionary responses to sexual selection intensity. Nature Publishing Group 2016-06-16 /pmc/articles/PMC4910101/ /pubmed/27306351 http://dx.doi.org/10.1038/srep28153 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article McNamara, Kathryn B. Robinson, Stephen P. Rosa, Márta E. Sloan, Nadia S. van Lieshout, Emile Simmons, Leigh W. Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title | Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title_full | Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title_fullStr | Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title_full_unstemmed | Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title_short | Male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, Callosobruchus maculatus |
title_sort | male-biased sex ratio does not promote increased sperm competitiveness in the seed beetle, callosobruchus maculatus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910101/ https://www.ncbi.nlm.nih.gov/pubmed/27306351 http://dx.doi.org/10.1038/srep28153 |
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