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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...
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/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. |
format | Online Article Text |
id | pubmed-9515635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
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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