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Coevolution of competing Callosobruchus species does not stabilize coexistence

Interspecific resource competition is expected to select for divergence in resource use, weakening interspecific relative to intraspecific competition, thus promoting stable coexistence. More broadly, because interspecific competition reduces fitness, any mechanism of interspecific competition shoul...

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Autores principales: Hausch, Stephen J., Fox, Jeremy W., Vamosi, Steven M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574802/
https://www.ncbi.nlm.nih.gov/pubmed/28861255
http://dx.doi.org/10.1002/ece3.3003
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author Hausch, Stephen J.
Fox, Jeremy W.
Vamosi, Steven M.
author_facet Hausch, Stephen J.
Fox, Jeremy W.
Vamosi, Steven M.
author_sort Hausch, Stephen J.
collection PubMed
description Interspecific resource competition is expected to select for divergence in resource use, weakening interspecific relative to intraspecific competition, thus promoting stable coexistence. More broadly, because interspecific competition reduces fitness, any mechanism of interspecific competition should generate selection favoring traits that weaken interspecific competition. However, species also can adapt to competition by increasing their competitive ability, potentially destabilizing coexistence. We reared two species of bean beetles, the specialist Callosobruchus maculatus and the generalist C. chinensis, in allopatry and sympatry on a mixture of adzuki beans and lentils, and assayed mutual invasibility after four, eight, and twelve generations of evolution. Contrary to the expectation that coevolution of competitors will weaken interspecific competition, the rate of mutual invasibility did not differ between sympatry and allopatry. Rather, the invasion rate of C. chinensis, but not C. maculatus, increased with duration of evolution, as C. chinensis adapted to lentils without experiencing reduced adaptation to adzuki beans, and regardless of the presence or absence of C. maculatus. Our results highlight that evolutionary responses to interspecific competition promote stable coexistence only under specific conditions that can be difficult to produce in practice.
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spelling pubmed-55748022017-08-31 Coevolution of competing Callosobruchus species does not stabilize coexistence Hausch, Stephen J. Fox, Jeremy W. Vamosi, Steven M. Ecol Evol Original Research Interspecific resource competition is expected to select for divergence in resource use, weakening interspecific relative to intraspecific competition, thus promoting stable coexistence. More broadly, because interspecific competition reduces fitness, any mechanism of interspecific competition should generate selection favoring traits that weaken interspecific competition. However, species also can adapt to competition by increasing their competitive ability, potentially destabilizing coexistence. We reared two species of bean beetles, the specialist Callosobruchus maculatus and the generalist C. chinensis, in allopatry and sympatry on a mixture of adzuki beans and lentils, and assayed mutual invasibility after four, eight, and twelve generations of evolution. Contrary to the expectation that coevolution of competitors will weaken interspecific competition, the rate of mutual invasibility did not differ between sympatry and allopatry. Rather, the invasion rate of C. chinensis, but not C. maculatus, increased with duration of evolution, as C. chinensis adapted to lentils without experiencing reduced adaptation to adzuki beans, and regardless of the presence or absence of C. maculatus. Our results highlight that evolutionary responses to interspecific competition promote stable coexistence only under specific conditions that can be difficult to produce in practice. John Wiley and Sons Inc. 2017-07-14 /pmc/articles/PMC5574802/ /pubmed/28861255 http://dx.doi.org/10.1002/ece3.3003 Text en © 2017 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Hausch, Stephen J.
Fox, Jeremy W.
Vamosi, Steven M.
Coevolution of competing Callosobruchus species does not stabilize coexistence
title Coevolution of competing Callosobruchus species does not stabilize coexistence
title_full Coevolution of competing Callosobruchus species does not stabilize coexistence
title_fullStr Coevolution of competing Callosobruchus species does not stabilize coexistence
title_full_unstemmed Coevolution of competing Callosobruchus species does not stabilize coexistence
title_short Coevolution of competing Callosobruchus species does not stabilize coexistence
title_sort coevolution of competing callosobruchus species does not stabilize coexistence
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5574802/
https://www.ncbi.nlm.nih.gov/pubmed/28861255
http://dx.doi.org/10.1002/ece3.3003
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