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Fossil basicranium clarifies the origin of the avian central nervous system and inner ear

Among terrestrial vertebrates, only crown birds (Neornithes) rival mammals in terms of relative brain size and behavioural complexity. Relatedly, the anatomy of the avian central nervous system and associated sensory structures, such as the vestibular system of the inner ear, are highly modified wit...

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Autores principales: Chiappe, Luis M., Navalón, Guillermo, Martinelli, Agustín G., Nava, William, Field, Daniel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515635/
https://www.ncbi.nlm.nih.gov/pubmed/36168759
http://dx.doi.org/10.1098/rspb.2022.1398
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author Chiappe, Luis M.
Navalón, Guillermo
Martinelli, Agustín G.
Nava, William
Field, Daniel J.
author_facet Chiappe, Luis M.
Navalón, Guillermo
Martinelli, Agustín G.
Nava, William
Field, Daniel J.
author_sort Chiappe, Luis M.
collection PubMed
description Among terrestrial vertebrates, only crown birds (Neornithes) rival mammals in terms of relative brain size and behavioural complexity. Relatedly, the anatomy of the avian central nervous system and associated sensory structures, such as the vestibular system of the inner ear, are highly modified with respect to those of other extant reptile lineages. However, a dearth of three-dimensional Mesozoic fossils has limited our knowledge of the origins of the distinctive endocranial structures of crown birds. Traits such as an expanded, flexed brain, a ventral connection between the brain and spinal column, and a modified vestibular system have been regarded as exclusive to Neornithes. Here, we demonstrate all of these ‘advanced’ traits in an undistorted braincase from an Upper Cretaceous enantiornithine bonebed in southeastern Brazil. Our discovery suggests that these crown bird-like endocranial traits may have originated prior to the split between Enantiornithes and the more crownward portion of avian phylogeny over 140 Ma, while coexisting with a remarkably plesiomorphic cranial base and posterior palate region. Altogether, our results support the interpretation that the distinctive endocranial morphologies of crown birds and their Mesozoic relatives are affected by complex trade-offs between spatial constraints during development.
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spelling pubmed-95156352022-09-28 Fossil basicranium clarifies the origin of the avian central nervous system and inner ear Chiappe, Luis M. Navalón, Guillermo Martinelli, Agustín G. Nava, William Field, Daniel J. Proc Biol Sci Palaeobiology Among terrestrial vertebrates, only crown birds (Neornithes) rival mammals in terms of relative brain size and behavioural complexity. Relatedly, the anatomy of the avian central nervous system and associated sensory structures, such as the vestibular system of the inner ear, are highly modified with respect to those of other extant reptile lineages. However, a dearth of three-dimensional Mesozoic fossils has limited our knowledge of the origins of the distinctive endocranial structures of crown birds. Traits such as an expanded, flexed brain, a ventral connection between the brain and spinal column, and a modified vestibular system have been regarded as exclusive to Neornithes. Here, we demonstrate all of these ‘advanced’ traits in an undistorted braincase from an Upper Cretaceous enantiornithine bonebed in southeastern Brazil. Our discovery suggests that these crown bird-like endocranial traits may have originated prior to the split between Enantiornithes and the more crownward portion of avian phylogeny over 140 Ma, while coexisting with a remarkably plesiomorphic cranial base and posterior palate region. Altogether, our results support the interpretation that the distinctive endocranial morphologies of crown birds and their Mesozoic relatives are affected by complex trade-offs between spatial constraints during development. The Royal Society 2022-09-28 2022-09-28 /pmc/articles/PMC9515635/ /pubmed/36168759 http://dx.doi.org/10.1098/rspb.2022.1398 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 Palaeobiology
Chiappe, Luis M.
Navalón, Guillermo
Martinelli, Agustín G.
Nava, William
Field, Daniel J.
Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title_full Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title_fullStr Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title_full_unstemmed Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title_short Fossil basicranium clarifies the origin of the avian central nervous system and inner ear
title_sort fossil basicranium clarifies the origin of the avian central nervous system and inner ear
topic Palaeobiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515635/
https://www.ncbi.nlm.nih.gov/pubmed/36168759
http://dx.doi.org/10.1098/rspb.2022.1398
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