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Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds
Birds are characterized by evolutionary specializations of both locomotion (e.g., flapping flight) and digestive system (toothless, crop, and gizzard), while the potential selection pressures responsible for these evolutionary specializations remain unclear. Here we used a recently developed molecul...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119460/ https://www.ncbi.nlm.nih.gov/pubmed/33986452 http://dx.doi.org/10.1038/s42003-021-02067-4 |
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author | Wu, Yonghua |
author_facet | Wu, Yonghua |
author_sort | Wu, Yonghua |
collection | PubMed |
description | Birds are characterized by evolutionary specializations of both locomotion (e.g., flapping flight) and digestive system (toothless, crop, and gizzard), while the potential selection pressures responsible for these evolutionary specializations remain unclear. Here we used a recently developed molecular phyloecological method to reconstruct the diets of the ancestral archosaur and of the common ancestor of living birds (CALB). Our results suggest a trophic shift from carnivory to herbivory (fruit, seed, and/or nut eater) at the archosaur-to-bird transition. The evolutionary shift of the CALB to herbivory may have essentially made them become a low-level consumer and, consequently, subject to relatively high predation risk from potential predators such as gliding non-avian maniraptorans, from which birds descended. Under the relatively high predation pressure, ancestral birds with gliding capability may have then evolved not only flapping flight as a possible anti-predator strategy against gliding predatory non-avian maniraptorans but also the specialized digestive system as an evolutionary tradeoff of maximizing foraging efficiency and minimizing predation risk. Our results suggest that the powered flight and specialized digestive system of birds may have evolved as a result of their tropic shift-associated predation pressure. |
format | Online Article Text |
id | pubmed-8119460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81194602021-05-14 Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds Wu, Yonghua Commun Biol Article Birds are characterized by evolutionary specializations of both locomotion (e.g., flapping flight) and digestive system (toothless, crop, and gizzard), while the potential selection pressures responsible for these evolutionary specializations remain unclear. Here we used a recently developed molecular phyloecological method to reconstruct the diets of the ancestral archosaur and of the common ancestor of living birds (CALB). Our results suggest a trophic shift from carnivory to herbivory (fruit, seed, and/or nut eater) at the archosaur-to-bird transition. The evolutionary shift of the CALB to herbivory may have essentially made them become a low-level consumer and, consequently, subject to relatively high predation risk from potential predators such as gliding non-avian maniraptorans, from which birds descended. Under the relatively high predation pressure, ancestral birds with gliding capability may have then evolved not only flapping flight as a possible anti-predator strategy against gliding predatory non-avian maniraptorans but also the specialized digestive system as an evolutionary tradeoff of maximizing foraging efficiency and minimizing predation risk. Our results suggest that the powered flight and specialized digestive system of birds may have evolved as a result of their tropic shift-associated predation pressure. Nature Publishing Group UK 2021-05-13 /pmc/articles/PMC8119460/ /pubmed/33986452 http://dx.doi.org/10.1038/s42003-021-02067-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Yonghua Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title | Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title_full | Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title_fullStr | Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title_full_unstemmed | Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title_short | Molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
title_sort | molecular phyloecology suggests a trophic shift concurrent with the evolution of the first birds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119460/ https://www.ncbi.nlm.nih.gov/pubmed/33986452 http://dx.doi.org/10.1038/s42003-021-02067-4 |
work_keys_str_mv | AT wuyonghua molecularphyloecologysuggestsatrophicshiftconcurrentwiththeevolutionofthefirstbirds |