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Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement

Interspecific competition for shared resources should select for evolutionary divergence in resource use between competing species, termed character displacement. Many purported examples of character displacement exist, but few completely rule out alternative explanations. We reared genetically dive...

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Autores principales: Hausch, Stephen J., Vamosi, Steven M., Fox, Jeremy W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160166/
https://www.ncbi.nlm.nih.gov/pubmed/32313631
http://dx.doi.org/10.1002/ece3.6164
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author Hausch, Stephen J.
Vamosi, Steven M.
Fox, Jeremy W.
author_facet Hausch, Stephen J.
Vamosi, Steven M.
Fox, Jeremy W.
author_sort Hausch, Stephen J.
collection PubMed
description Interspecific competition for shared resources should select for evolutionary divergence in resource use between competing species, termed character displacement. Many purported examples of character displacement exist, but few completely rule out alternative explanations. We reared genetically diverse populations of two species of bean beetles, Callosobruchus maculatus and Callosobruchus chinensis, in allopatry and sympatry on a mixture of adzuki beans and lentils, and assayed oviposition preference and other phenotypic traits after four, eight, and twelve generations of (co)evolution. C. maculatus specializes on adzuki beans; the generalist C. chinensis uses both beans. C. chinensis growing in allopatry emerged equally from both bean species. In sympatry, the two species competing strongly and coexisted via strong realized resource partitioning, with C. chinensis emerging almost exclusively from lentils and C. maculatus emerging almost exclusively from adzuki beans. However, oviposition preferences, larval survival traits, and larval development rates in both beetle species did not vary consistently between allopatric versus sympatric treatments. Rather, traits evolved in treatment‐independent fashion, with several traits exhibiting reversals in their evolutionary trajectories. For example, C. chinensis initially evolved a slower egg‐to‐adult development rate on adzuki beans in both allopatry and sympatry, then subsequently evolved back toward the faster ancestral development rate. Lack of character displacement is consistent with a previous similar experiment in bean beetles and may reflect lack of evolutionary trade‐offs in resource use. However, evolutionary reversals were unexpected and remain unexplained. Together with other empirical and theoretical work, our results illustrate the stringency of the conditions for character displacement.
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spelling pubmed-71601662020-04-20 Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement Hausch, Stephen J. Vamosi, Steven M. Fox, Jeremy W. Ecol Evol Original Research Interspecific competition for shared resources should select for evolutionary divergence in resource use between competing species, termed character displacement. Many purported examples of character displacement exist, but few completely rule out alternative explanations. We reared genetically diverse populations of two species of bean beetles, Callosobruchus maculatus and Callosobruchus chinensis, in allopatry and sympatry on a mixture of adzuki beans and lentils, and assayed oviposition preference and other phenotypic traits after four, eight, and twelve generations of (co)evolution. C. maculatus specializes on adzuki beans; the generalist C. chinensis uses both beans. C. chinensis growing in allopatry emerged equally from both bean species. In sympatry, the two species competing strongly and coexisted via strong realized resource partitioning, with C. chinensis emerging almost exclusively from lentils and C. maculatus emerging almost exclusively from adzuki beans. However, oviposition preferences, larval survival traits, and larval development rates in both beetle species did not vary consistently between allopatric versus sympatric treatments. Rather, traits evolved in treatment‐independent fashion, with several traits exhibiting reversals in their evolutionary trajectories. For example, C. chinensis initially evolved a slower egg‐to‐adult development rate on adzuki beans in both allopatry and sympatry, then subsequently evolved back toward the faster ancestral development rate. Lack of character displacement is consistent with a previous similar experiment in bean beetles and may reflect lack of evolutionary trade‐offs in resource use. However, evolutionary reversals were unexpected and remain unexplained. Together with other empirical and theoretical work, our results illustrate the stringency of the conditions for character displacement. John Wiley and Sons Inc. 2020-03-13 /pmc/articles/PMC7160166/ /pubmed/32313631 http://dx.doi.org/10.1002/ece3.6164 Text en © 2020 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the 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.
Vamosi, Steven M.
Fox, Jeremy W.
Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title_full Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title_fullStr Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title_full_unstemmed Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title_short Experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
title_sort experimental evolution of competing bean beetle species reveals long‐term reversals of short‐term evolution, but no consistent character displacement
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160166/
https://www.ncbi.nlm.nih.gov/pubmed/32313631
http://dx.doi.org/10.1002/ece3.6164
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