Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera)
Abstract Background Self-powered flight is one of the most energy-intensive types of locomotion found in vertebrates. It is also associated with a range of extreme morpho-physiological adaptations that evolved independently in three different vertebrate groups. Considering that development acts as a...
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doaj-919ad8d5e6974df691526af9b2b4523e2021-09-02T12:08:39ZengBMCBMC Evolutionary Biology1471-21482019-03-0119111710.1186/s12862-019-1396-1Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera)Camilo López-Aguirre0Suzanne J. Hand1Daisuke Koyabu2Nguyen Truong Son3Laura A. B. Wilson4PANGEA Research Centre, School of Biological, Earth & Environmental Sciences, University of New South WalesPANGEA Research Centre, School of Biological, Earth & Environmental Sciences, University of New South WalesUniversity Museum, University of TokyoDepartment of Vertebrate Zoology, Institute of Ecology and Biological Resources, Vietnam Academy of Sciences and TechnologyPANGEA Research Centre, School of Biological, Earth & Environmental Sciences, University of New South WalesAbstract Background Self-powered flight is one of the most energy-intensive types of locomotion found in vertebrates. It is also associated with a range of extreme morpho-physiological adaptations that evolved independently in three different vertebrate groups. Considering that development acts as a bridge between the genotype and phenotype on which selection acts, studying the ossification of the postcranium can potentially illuminate our understanding of bat flight evolution. However, the ontogenetic basis of vertebrate flight remains largely understudied. Advances in quantitative analysis of sequence heterochrony and morphogenetic growth have created novel approaches to study the developmental basis of diversification and the evolvability of skeletal morphogenesis. Assessing the presence of ontogenetic disparity, integration and modularity from an evolutionary approach allows assessing whether flight may have resulted in evolutionary differences in the magnitude and mode of development in bats. Results We quantitatively compared the prenatal ossification of the postcranium (24 bones) between bats (14 species), non-volant mammals (11 species) and birds (14 species), combining for the first time prenatal sequence heterochrony and developmental growth data. Sequence heterochrony was found across groups, showing that bat postcranial development shares patterns found in other flying vertebrates but also those in non-volant mammals. In bats, modularity was found as an axial-appendicular partition, resembling a mammalian pattern of developmental modularity and suggesting flight did not repattern prenatal postcranial covariance in bats. Conclusions Combining prenatal data from 14 bat species, this study represents the most comprehensive quantitative analysis of chiropteran ossification to date. Heterochrony between the wing and leg in bats could reflect functional needs of the newborn, rather than ecological aspects of the adult. Bats share similarities with birds in the development of structures involved in flight (i.e. handwing and sternum), suggesting that flight altriciality and early ossification of pedal phalanges and sternum are common across flying vertebrates. These results indicate that the developmental modularity found in bats facilitates intramodular phenotypic diversification of the skeleton. Integration and disparity increased across developmental time in bats. We also found a delay in the ossification of highly adaptable and evolvable regions (e.g. handwing and sternum) that are directly associated with flight performance.http://link.springer.com/article/10.1186/s12862-019-1396-1Sequence heterochronyPostcranial developmentPrenatal growthModularityIntegrationOntogeny |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Camilo López-Aguirre Suzanne J. Hand Daisuke Koyabu Nguyen Truong Son Laura A. B. Wilson |
spellingShingle |
Camilo López-Aguirre Suzanne J. Hand Daisuke Koyabu Nguyen Truong Son Laura A. B. Wilson Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) BMC Evolutionary Biology Sequence heterochrony Postcranial development Prenatal growth Modularity Integration Ontogeny |
author_facet |
Camilo López-Aguirre Suzanne J. Hand Daisuke Koyabu Nguyen Truong Son Laura A. B. Wilson |
author_sort |
Camilo López-Aguirre |
title |
Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) |
title_short |
Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) |
title_full |
Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) |
title_fullStr |
Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) |
title_full_unstemmed |
Postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (Chiroptera) |
title_sort |
postcranial heterochrony, modularity, integration and disparity in the prenatal ossification in bats (chiroptera) |
publisher |
BMC |
series |
BMC Evolutionary Biology |
issn |
1471-2148 |
publishDate |
2019-03-01 |
description |
Abstract Background Self-powered flight is one of the most energy-intensive types of locomotion found in vertebrates. It is also associated with a range of extreme morpho-physiological adaptations that evolved independently in three different vertebrate groups. Considering that development acts as a bridge between the genotype and phenotype on which selection acts, studying the ossification of the postcranium can potentially illuminate our understanding of bat flight evolution. However, the ontogenetic basis of vertebrate flight remains largely understudied. Advances in quantitative analysis of sequence heterochrony and morphogenetic growth have created novel approaches to study the developmental basis of diversification and the evolvability of skeletal morphogenesis. Assessing the presence of ontogenetic disparity, integration and modularity from an evolutionary approach allows assessing whether flight may have resulted in evolutionary differences in the magnitude and mode of development in bats. Results We quantitatively compared the prenatal ossification of the postcranium (24 bones) between bats (14 species), non-volant mammals (11 species) and birds (14 species), combining for the first time prenatal sequence heterochrony and developmental growth data. Sequence heterochrony was found across groups, showing that bat postcranial development shares patterns found in other flying vertebrates but also those in non-volant mammals. In bats, modularity was found as an axial-appendicular partition, resembling a mammalian pattern of developmental modularity and suggesting flight did not repattern prenatal postcranial covariance in bats. Conclusions Combining prenatal data from 14 bat species, this study represents the most comprehensive quantitative analysis of chiropteran ossification to date. Heterochrony between the wing and leg in bats could reflect functional needs of the newborn, rather than ecological aspects of the adult. Bats share similarities with birds in the development of structures involved in flight (i.e. handwing and sternum), suggesting that flight altriciality and early ossification of pedal phalanges and sternum are common across flying vertebrates. These results indicate that the developmental modularity found in bats facilitates intramodular phenotypic diversification of the skeleton. Integration and disparity increased across developmental time in bats. We also found a delay in the ossification of highly adaptable and evolvable regions (e.g. handwing and sternum) that are directly associated with flight performance. |
topic |
Sequence heterochrony Postcranial development Prenatal growth Modularity Integration Ontogeny |
url |
http://link.springer.com/article/10.1186/s12862-019-1396-1 |
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