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Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts
BACKGROUND: Male killing endosymbionts manipulate their arthropod host reproduction by only allowing female embryos to develop into infected females and killing all male offspring. Because the resulting change in sex ratio is expected to affect the evolution of sex-specific dispersal, we investigate...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633281/ https://www.ncbi.nlm.nih.gov/pubmed/19149895 http://dx.doi.org/10.1186/1471-2148-9-16 |
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author | Bonte, Dries Hovestadt, Thomas Poethke, Hans-Joachim |
author_facet | Bonte, Dries Hovestadt, Thomas Poethke, Hans-Joachim |
author_sort | Bonte, Dries |
collection | PubMed |
description | BACKGROUND: Male killing endosymbionts manipulate their arthropod host reproduction by only allowing female embryos to develop into infected females and killing all male offspring. Because the resulting change in sex ratio is expected to affect the evolution of sex-specific dispersal, we investigated under which environmental conditions strong sex-biased dispersal would emerge, and how this would affect host and endosymbiont metapopulation persistence. RESULTS: We simulated host-endosymbiont metapopulation dynamics in an individual-based model, in which dispersal rates are allowed to evolve independently for the two sexes. Prominent male-biased dispersal emerges under conditions of low environmental stochasticity and high dispersal mortality. By applying a reshuffling algorithm, we show that kin-competition is a major driver of this evolutionary pattern because of the high within-population relatedness of males compared to those of females. Moreover, the evolution of sex-specific dispersal rescues metapopulations from extinction by (i) reducing endosymbiont fixation rates and (ii) by enhancing the extinction of endosymbionts within metapopulations that are characterized by low environmental stochasticity. CONCLUSION: Male killing endosymbionts induce the evolution of sex-specific dispersal, with prominent male-biased dispersal under conditions of low environmental stochasticity and high dispersal mortality. This male-biased dispersal emerges from stronger kin-competition in males compared to females and induces an evolutionary rescue mechanism. |
format | Text |
id | pubmed-2633281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26332812009-02-02 Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts Bonte, Dries Hovestadt, Thomas Poethke, Hans-Joachim BMC Evol Biol Research Article BACKGROUND: Male killing endosymbionts manipulate their arthropod host reproduction by only allowing female embryos to develop into infected females and killing all male offspring. Because the resulting change in sex ratio is expected to affect the evolution of sex-specific dispersal, we investigated under which environmental conditions strong sex-biased dispersal would emerge, and how this would affect host and endosymbiont metapopulation persistence. RESULTS: We simulated host-endosymbiont metapopulation dynamics in an individual-based model, in which dispersal rates are allowed to evolve independently for the two sexes. Prominent male-biased dispersal emerges under conditions of low environmental stochasticity and high dispersal mortality. By applying a reshuffling algorithm, we show that kin-competition is a major driver of this evolutionary pattern because of the high within-population relatedness of males compared to those of females. Moreover, the evolution of sex-specific dispersal rescues metapopulations from extinction by (i) reducing endosymbiont fixation rates and (ii) by enhancing the extinction of endosymbionts within metapopulations that are characterized by low environmental stochasticity. CONCLUSION: Male killing endosymbionts induce the evolution of sex-specific dispersal, with prominent male-biased dispersal under conditions of low environmental stochasticity and high dispersal mortality. This male-biased dispersal emerges from stronger kin-competition in males compared to females and induces an evolutionary rescue mechanism. BioMed Central 2009-01-16 /pmc/articles/PMC2633281/ /pubmed/19149895 http://dx.doi.org/10.1186/1471-2148-9-16 Text en Copyright © 2009 Bonte et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bonte, Dries Hovestadt, Thomas Poethke, Hans-Joachim Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title | Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title_full | Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title_fullStr | Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title_full_unstemmed | Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title_short | Sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
title_sort | sex-specific dispersal and evolutionary rescue in metapopulations infected by male killing endosymbionts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633281/ https://www.ncbi.nlm.nih.gov/pubmed/19149895 http://dx.doi.org/10.1186/1471-2148-9-16 |
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