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The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end

Trapliners are pollinators that visit widely dispersed flowers along circuitous foraging routes. The evolution of traplining in hummingbirds is thought to entail morphological specialization through the reciprocal coevolution of longer bills with the long-tubed flowers of widely dispersed plant spec...

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Autores principales: Rombaut, Louie M. K., Capp, Elliot J. R., Hughes, Emma C., Varley, Zoë K., Beckerman, Andrew P., Cooper, Natalie, Thomas, Gavin H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767203/
https://www.ncbi.nlm.nih.gov/pubmed/35042413
http://dx.doi.org/10.1098/rspb.2021.2484
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author Rombaut, Louie M. K.
Capp, Elliot J. R.
Hughes, Emma C.
Varley, Zoë K.
Beckerman, Andrew P.
Cooper, Natalie
Thomas, Gavin H.
author_facet Rombaut, Louie M. K.
Capp, Elliot J. R.
Hughes, Emma C.
Varley, Zoë K.
Beckerman, Andrew P.
Cooper, Natalie
Thomas, Gavin H.
author_sort Rombaut, Louie M. K.
collection PubMed
description Trapliners are pollinators that visit widely dispersed flowers along circuitous foraging routes. The evolution of traplining in hummingbirds is thought to entail morphological specialization through the reciprocal coevolution of longer bills with the long-tubed flowers of widely dispersed plant species. Specialization, such as that exhibited by traplining hummingbirds, is often viewed as both irreversible and an evolutionary dead end. We tested these predictions in a macroevolutionary framework. Specifically, we assessed the relationship between beak morphology and foraging and tested whether transitions to traplining are irreversible and lead to lower rates of diversification as predicted by the hypothesis that specialization is an evolutionary dead end. We find that there have been multiple independent transitions to traplining across the hummingbird phylogeny, but reversals have been rare or incomplete at best. Multiple independent lineages of trapliners have become morphologically specialized, convergently evolving relatively large bills for their body size. Traplining is not an evolutionary dead end however, since trapliners continue to give rise to new traplining species at a rate comparable to non-trapliners.
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spelling pubmed-87672032022-02-03 The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end Rombaut, Louie M. K. Capp, Elliot J. R. Hughes, Emma C. Varley, Zoë K. Beckerman, Andrew P. Cooper, Natalie Thomas, Gavin H. Proc Biol Sci Evolution Trapliners are pollinators that visit widely dispersed flowers along circuitous foraging routes. The evolution of traplining in hummingbirds is thought to entail morphological specialization through the reciprocal coevolution of longer bills with the long-tubed flowers of widely dispersed plant species. Specialization, such as that exhibited by traplining hummingbirds, is often viewed as both irreversible and an evolutionary dead end. We tested these predictions in a macroevolutionary framework. Specifically, we assessed the relationship between beak morphology and foraging and tested whether transitions to traplining are irreversible and lead to lower rates of diversification as predicted by the hypothesis that specialization is an evolutionary dead end. We find that there have been multiple independent transitions to traplining across the hummingbird phylogeny, but reversals have been rare or incomplete at best. Multiple independent lineages of trapliners have become morphologically specialized, convergently evolving relatively large bills for their body size. Traplining is not an evolutionary dead end however, since trapliners continue to give rise to new traplining species at a rate comparable to non-trapliners. The Royal Society 2022-01-26 2022-01-19 /pmc/articles/PMC8767203/ /pubmed/35042413 http://dx.doi.org/10.1098/rspb.2021.2484 Text en © 2022 The Authors. https://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/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Rombaut, Louie M. K.
Capp, Elliot J. R.
Hughes, Emma C.
Varley, Zoë K.
Beckerman, Andrew P.
Cooper, Natalie
Thomas, Gavin H.
The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title_full The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title_fullStr The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title_full_unstemmed The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title_short The evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
title_sort evolution of the traplining pollinator role in hummingbirds: specialization is not an evolutionary dead end
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8767203/
https://www.ncbi.nlm.nih.gov/pubmed/35042413
http://dx.doi.org/10.1098/rspb.2021.2484
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