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Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’
Living kangaroos, wallabies and rat-kangaroos (Macropodoidea) constitute the most ecologically diverse radiation of Australasian marsupials. Indeed, even their hallmark bipedal hopping gait has been variously modified for bounding, walking and climbing. However, the origins of this locomotory adapta...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408368/ https://www.ncbi.nlm.nih.gov/pubmed/30891280 http://dx.doi.org/10.1098/rsos.181617 |
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author | Den Boer, Wendy Campione, Nicolás E. Kear, Benjamin P. |
author_facet | Den Boer, Wendy Campione, Nicolás E. Kear, Benjamin P. |
author_sort | Den Boer, Wendy |
collection | PubMed |
description | Living kangaroos, wallabies and rat-kangaroos (Macropodoidea) constitute the most ecologically diverse radiation of Australasian marsupials. Indeed, even their hallmark bipedal hopping gait has been variously modified for bounding, walking and climbing. However, the origins of this locomotory adaptability are uncertain because skeletons of the most ancient macropodoids are exceptionally rare. Some of the stratigraphically oldest fossils have been attributed to Balbaridae—a clade of potentially quadrupedal stem macropodoids that became extinct during the late Miocene. Here we undertake the first assessment of balbarid locomotion using two-dimensional geometric morphometrics and a correlative multivariate analysis of linear measurements. We selected the astragalus and pedal digit IV ungual as proxies for primary gait because these elements are preserved in the only articulated balbarid skeleton, as well as some unusual early Miocene balbarid-like remains that resemble the bones of modern tree-kangaroos. Our results show that these fossils manifest character states indicative of contrasting locomotory capabilities. Furthermore, predictive modelling reveals similarities with extant macropodoids that employ either bipedal saltation and/or climbing. We interpret this as evidence for archetypal gait versatility, which probably integrated higher-speed hopping with slower-speed quadrupedal progression and varying degrees of scansoriality as independent specializations for life in forest and woodland settings. |
format | Online Article Text |
id | pubmed-6408368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-64083682019-03-19 Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ Den Boer, Wendy Campione, Nicolás E. Kear, Benjamin P. R Soc Open Sci Biology (Whole Organism) Living kangaroos, wallabies and rat-kangaroos (Macropodoidea) constitute the most ecologically diverse radiation of Australasian marsupials. Indeed, even their hallmark bipedal hopping gait has been variously modified for bounding, walking and climbing. However, the origins of this locomotory adaptability are uncertain because skeletons of the most ancient macropodoids are exceptionally rare. Some of the stratigraphically oldest fossils have been attributed to Balbaridae—a clade of potentially quadrupedal stem macropodoids that became extinct during the late Miocene. Here we undertake the first assessment of balbarid locomotion using two-dimensional geometric morphometrics and a correlative multivariate analysis of linear measurements. We selected the astragalus and pedal digit IV ungual as proxies for primary gait because these elements are preserved in the only articulated balbarid skeleton, as well as some unusual early Miocene balbarid-like remains that resemble the bones of modern tree-kangaroos. Our results show that these fossils manifest character states indicative of contrasting locomotory capabilities. Furthermore, predictive modelling reveals similarities with extant macropodoids that employ either bipedal saltation and/or climbing. We interpret this as evidence for archetypal gait versatility, which probably integrated higher-speed hopping with slower-speed quadrupedal progression and varying degrees of scansoriality as independent specializations for life in forest and woodland settings. The Royal Society 2019-02-06 /pmc/articles/PMC6408368/ /pubmed/30891280 http://dx.doi.org/10.1098/rsos.181617 Text en © 2019 The Authors. http://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/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biology (Whole Organism) Den Boer, Wendy Campione, Nicolás E. Kear, Benjamin P. Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title | Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title_full | Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title_fullStr | Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title_full_unstemmed | Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title_short | Climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
title_sort | climbing adaptations, locomotory disparity and ecological convergence in ancient stem ‘kangaroos’ |
topic | Biology (Whole Organism) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408368/ https://www.ncbi.nlm.nih.gov/pubmed/30891280 http://dx.doi.org/10.1098/rsos.181617 |
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