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Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait

Skeletal pneumaticity is a key feature of extant avian structure and biology, which first evolved among the non-flying archosaurian ancestors of birds. The widespread presence of air-filled bones across the postcranial skeleton is unique to birds among living vertebrates, but the true extent of skel...

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Autores principales: Burton, Maria Grace P., Benson, Roger B. J., Field, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015330/
https://www.ncbi.nlm.nih.gov/pubmed/36919426
http://dx.doi.org/10.1098/rspb.2023.0160
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author Burton, Maria Grace P.
Benson, Roger B. J.
Field, Daniel J.
author_facet Burton, Maria Grace P.
Benson, Roger B. J.
Field, Daniel J.
author_sort Burton, Maria Grace P.
collection PubMed
description Skeletal pneumaticity is a key feature of extant avian structure and biology, which first evolved among the non-flying archosaurian ancestors of birds. The widespread presence of air-filled bones across the postcranial skeleton is unique to birds among living vertebrates, but the true extent of skeletal pneumaticity has never been quantitatively investigated—hindering fundamental insights into the evolution of this key avian feature. Here, we use microCT scans of fresh, frozen birds to directly quantify the fraction of humerus volume occupied by air across a phylogenetically diverse taxon sample to test longstanding hypotheses regarding the evolution and function of avian skeletal pneumatization. Among other insights, we document weak positive allometry of internal air volume with humeral size among pneumatized humeri and provide strong support that humeral size, body mass, aquatic diving, and the presence or absence of pneumaticity all have independent effects on cortical bone thickness. Our quantitative evaluation of humeral pneumaticity across extant avian phylogeny sheds new light on the evolution and ontogenetic progression of an important aspect of avian skeletal architecture, and suggests that the last common ancestor of crown birds possessed a highly pneumatized humerus.
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spelling pubmed-100153302023-03-16 Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait Burton, Maria Grace P. Benson, Roger B. J. Field, Daniel J. Proc Biol Sci Morphology and Biomechanics Skeletal pneumaticity is a key feature of extant avian structure and biology, which first evolved among the non-flying archosaurian ancestors of birds. The widespread presence of air-filled bones across the postcranial skeleton is unique to birds among living vertebrates, but the true extent of skeletal pneumaticity has never been quantitatively investigated—hindering fundamental insights into the evolution of this key avian feature. Here, we use microCT scans of fresh, frozen birds to directly quantify the fraction of humerus volume occupied by air across a phylogenetically diverse taxon sample to test longstanding hypotheses regarding the evolution and function of avian skeletal pneumatization. Among other insights, we document weak positive allometry of internal air volume with humeral size among pneumatized humeri and provide strong support that humeral size, body mass, aquatic diving, and the presence or absence of pneumaticity all have independent effects on cortical bone thickness. Our quantitative evaluation of humeral pneumaticity across extant avian phylogeny sheds new light on the evolution and ontogenetic progression of an important aspect of avian skeletal architecture, and suggests that the last common ancestor of crown birds possessed a highly pneumatized humerus. The Royal Society 2023-03-29 2023-03-15 /pmc/articles/PMC10015330/ /pubmed/36919426 http://dx.doi.org/10.1098/rspb.2023.0160 Text en © 2023 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 Morphology and Biomechanics
Burton, Maria Grace P.
Benson, Roger B. J.
Field, Daniel J.
Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title_full Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title_fullStr Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title_full_unstemmed Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title_short Direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
title_sort direct quantification of skeletal pneumaticity illuminates ecological drivers of a key avian trait
topic Morphology and Biomechanics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015330/
https://www.ncbi.nlm.nih.gov/pubmed/36919426
http://dx.doi.org/10.1098/rspb.2023.0160
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