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The signature of competition in ecomorphological traits across the avian radiation
Competition for shared resources represents a fundamental driver of biological diversity. However, the tempo and mode of phenotypic evolution in deep-time has been predominantly investigated using trait evolutionary models which assume that lineages evolve independently from each other. Consequently...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735287/ https://www.ncbi.nlm.nih.gov/pubmed/33171084 http://dx.doi.org/10.1098/rspb.2020.1585 |
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author | Chira, A. M. Cooney, C. R. Bright, J. A. Capp, E. J. R. Hughes, E. C. Moody, C. J. A. Nouri, L. O. Varley, Z. K. Thomas, G. H. |
author_facet | Chira, A. M. Cooney, C. R. Bright, J. A. Capp, E. J. R. Hughes, E. C. Moody, C. J. A. Nouri, L. O. Varley, Z. K. Thomas, G. H. |
author_sort | Chira, A. M. |
collection | PubMed |
description | Competition for shared resources represents a fundamental driver of biological diversity. However, the tempo and mode of phenotypic evolution in deep-time has been predominantly investigated using trait evolutionary models which assume that lineages evolve independently from each other. Consequently, the role of species interactions in driving macroevolutionary dynamics remains poorly understood. Here, we quantify the prevalence for signatures of competition between related species in the evolution of ecomorphological traits across the bird radiation. We find that mechanistic trait models accounting for the effect of species interactions on phenotypic divergence provide the best fit for the data on at least one trait axis in 27 out of 59 clades ranging between 21 and 195 species. Where it occurs, the signature of competition generally coincides with positive species diversity-dependence, driven by the accumulation of lineages with similar ecologies, and we find scarce evidence for trait-dependent or negative diversity-dependent phenotypic evolution. Overall, our results suggest that the footprint of interspecific competition is often eroded in long-term patterns of phenotypic diversification, and that other selection pressures may predominantly shape ecomorphological diversity among extant species at macroevolutionary scales. |
format | Online Article Text |
id | pubmed-7735287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77352872020-12-28 The signature of competition in ecomorphological traits across the avian radiation Chira, A. M. Cooney, C. R. Bright, J. A. Capp, E. J. R. Hughes, E. C. Moody, C. J. A. Nouri, L. O. Varley, Z. K. Thomas, G. H. Proc Biol Sci Evolution Competition for shared resources represents a fundamental driver of biological diversity. However, the tempo and mode of phenotypic evolution in deep-time has been predominantly investigated using trait evolutionary models which assume that lineages evolve independently from each other. Consequently, the role of species interactions in driving macroevolutionary dynamics remains poorly understood. Here, we quantify the prevalence for signatures of competition between related species in the evolution of ecomorphological traits across the bird radiation. We find that mechanistic trait models accounting for the effect of species interactions on phenotypic divergence provide the best fit for the data on at least one trait axis in 27 out of 59 clades ranging between 21 and 195 species. Where it occurs, the signature of competition generally coincides with positive species diversity-dependence, driven by the accumulation of lineages with similar ecologies, and we find scarce evidence for trait-dependent or negative diversity-dependent phenotypic evolution. Overall, our results suggest that the footprint of interspecific competition is often eroded in long-term patterns of phenotypic diversification, and that other selection pressures may predominantly shape ecomorphological diversity among extant species at macroevolutionary scales. The Royal Society 2020-11-11 2020-11-11 /pmc/articles/PMC7735287/ /pubmed/33171084 http://dx.doi.org/10.1098/rspb.2020.1585 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Chira, A. M. Cooney, C. R. Bright, J. A. Capp, E. J. R. Hughes, E. C. Moody, C. J. A. Nouri, L. O. Varley, Z. K. Thomas, G. H. The signature of competition in ecomorphological traits across the avian radiation |
title | The signature of competition in ecomorphological traits across the avian radiation |
title_full | The signature of competition in ecomorphological traits across the avian radiation |
title_fullStr | The signature of competition in ecomorphological traits across the avian radiation |
title_full_unstemmed | The signature of competition in ecomorphological traits across the avian radiation |
title_short | The signature of competition in ecomorphological traits across the avian radiation |
title_sort | signature of competition in ecomorphological traits across the avian radiation |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735287/ https://www.ncbi.nlm.nih.gov/pubmed/33171084 http://dx.doi.org/10.1098/rspb.2020.1585 |
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