Literature DB >> 22356676

Do different disparity proxies converge on a common signal? Insights from the cranial morphometrics and evolutionary history of Pterosauria (Diapsida: Archosauria).

C Foth1, S L Brusatte, R J Butler.   

Abstract

Disparity, or morphological diversity, is often quantified by evolutionary biologists investigating the macroevolutionary history of clades over geological timescales. Disparity is typically quantified using proxies for morphology, such as measurements, discrete anatomical characters, or geometric morphometrics. If different proxies produce differing results, then the accurate quantification of disparity in deep time may be problematic. However, despite this, few studies have attempted to examine disparity of a single clade using multiple morphological proxies. Here, as a case study for this question, we examine the disparity of the volant Mesozoic fossil reptile clade Pterosauria, an intensively studied group that achieved substantial morphological, ecological and taxonomic diversity during their 145+ million-year evolutionary history. We characterize broadscale patterns of cranial morphological disparity for pterosaurs for the first time using landmark-based geometric morphometrics and make comparisons to calculations of pterosaur disparity based on alternative metrics. Landmark-based disparity calculations suggest that monofenestratan pterosaurs were more diverse cranially than basal non-monofenestratan pterosaurs (at least when the aberrant anurognathids are excluded), and that peak cranial disparity may have occurred in the Early Cretaceous, relatively late in pterosaur evolution. Significantly, our cranial disparity results are broadly congruent with those based on whole skeleton discrete character and limb proportion data sets, indicating that these divergent approaches document a consistent pattern of pterosaur morphological evolution. Therefore, pterosaurs provide an exemplar case demonstrating that different proxies for morphological form can converge on the same disparity signal, which is encouraging because often only one such proxy is available for extinct clades represented by fossils. Furthermore, mapping phylogeny into cranial morphospace demonstrates that pterosaur cranial morphology is significantly correlated with, and potentially constrained by, phylogenetic relationships.
© 2012 The Authors. Journal of Evolutionary Biology © 2012 European Society For Evolutionary Biology.

Entities:  

Mesh:

Year:  2012        PMID: 22356676     DOI: 10.1111/j.1420-9101.2012.02479.x

Source DB:  PubMed          Journal:  J Evol Biol        ISSN: 1010-061X            Impact factor:   2.411


  17 in total

1.  Clades reach highest morphological disparity early in their evolution.

Authors:  Martin Hughes; Sylvain Gerber; Matthew Albion Wills
Journal:  Proc Natl Acad Sci U S A       Date:  2013-07-24       Impact factor: 11.205

2.  Slow and steady: the evolution of cranial disparity in fossil and recent turtles.

Authors:  Christian Foth; Walter G Joyce
Journal:  Proc Biol Sci       Date:  2016-11-30       Impact factor: 5.349

3.  The good, the bad, and the ugly: the influence of skull reconstructions and intraspecific variability in studies of cranial morphometrics in theropods and Basal saurischians.

Authors:  Christian Foth; Oliver W M Rauhut
Journal:  PLoS One       Date:  2013-08-08       Impact factor: 3.240

4.  Morphological diversity in tenrecs (Afrosoricida, Tenrecidae): comparing tenrec skull diversity to their closest relatives.

Authors:  Sive Finlay; Natalie Cooper
Journal:  PeerJ       Date:  2015-04-30       Impact factor: 2.984

5.  Morphological and biomechanical disparity of crocodile-line archosaurs following the end-Triassic extinction.

Authors:  Thomas L Stubbs; Stephanie E Pierce; Emily J Rayfield; Philip S L Anderson
Journal:  Proc Biol Sci       Date:  2013-09-11       Impact factor: 5.349

6.  Still slow, but even steadier: an update on the evolution of turtle cranial disparity interpolating shapes along branches.

Authors:  Christian Foth; Eduardo Ascarrunz; Walter G Joyce
Journal:  R Soc Open Sci       Date:  2017-11-29       Impact factor: 2.963

7.  Discrete and continuous character-based disparity analyses converge to the same macroevolutionary signal: a case study from captorhinids.

Authors:  Marco Romano; Neil Brocklehurst; Jörg Fröbisch
Journal:  Sci Rep       Date:  2017-12-13       Impact factor: 4.379

8.  Earliest filter-feeding pterosaur from the Jurassic of China and ecological evolution of Pterodactyloidea.

Authors:  Chang-Fu Zhou; Ke-Qin Gao; Hongyu Yi; Jinzhuang Xue; Quanguo Li; Richard C Fox
Journal:  R Soc Open Sci       Date:  2017-02-01       Impact factor: 2.963

9.  A Jurassic pterosaur from Patagonia and the origin of the pterodactyloid neurocranium.

Authors:  Laura Codorniú; Ariana Paulina Carabajal; Diego Pol; David Unwin; Oliver W M Rauhut
Journal:  PeerJ       Date:  2016-08-30       Impact factor: 2.984

10.  Preservational bias controls the fossil record of pterosaurs.

Authors:  Christopher D Dean; Philip D Mannion; Richard J Butler
Journal:  Palaeontology       Date:  2016-01-14       Impact factor: 4.073

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.