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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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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. |
format | Online Article Text |
id | pubmed-8767203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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