TY - JOUR
T1 - The ecological diversification and evolution of Teleosauroidea (Crocodylomorpha, Thalattosuchia), with insights into their mandibular biomechanics
AU - Johnson, Michela M.
AU - Foffa, Davide
AU - Young, Mark T.
AU - Brusatte, Stephen L.
N1 - Funding Information:
The authors would like to sincerely thank two anonymous reviewers and G. Jenkins (editor) for their helpful feedback and comments, which greatly improved the quality of the manuscript. We thank M. Williams (BRLSI), M. Riley (CAMSM), P. Tomlinson (DORCM), I. Werneburg (GPIT), G. Garcia, F. Guy and P. Vignaud (LPP), O. Mateus (MG), S. Etches (MJML), M. Wilmsen (MMG), R. Allain (MNHN), B. Thuy and R. Weis (MNHNL), S. Maidment (NHMUK), T. Mörs (NRM), J. Dridi (ONM), E. Howlett and H. Ketchum (OUMNH), G. Wass (PETMG), K. Lauprasert (PRC), and E. Maxwell and R. Schoch (SMNS) for access to specimens, and V. Lamarque (MMT) for photographs of Seldsienean megistorhynchus. MMJ is currently supported by the Alexander von Humboldt Foundation (CAN 1218253 HFST‐P) and her museum visits were funded by the Natural Sciences and Engineering Research Council of Canada (PGSD3‐487581‐2016), SYNTHESYS Project (FR‐TAF‐6577), the Small Grant Scheme (PA‐SW201601), the Paleontological Society “Stephen Jay Gould Award” Student Research Grant, and Richard Owen Research Fund by the Palaeontographical Society. DF’s museum visits were funded by the Small Grant Scheme “2015 Wood Award” (PASW201402), Systematics Research Fund and Richard Owen Research Fund by the Palaeontographical Society. SLB and MTY were supported by Leverhulme Trust Research Project grant (RPG‐2017‐167). Finally, we sincerely thank J. Schwab and E. Amson for help and instruction in RStudio, C. Foth and K. Dexter for statistical discussion and S. Evers for discussion on turtle evolution. Open Access funding enabled and organized by Projekt DEAL.
Funding Information:
The authors would like to sincerely thank two anonymous reviewers and G. Jenkins (editor) for their helpful feedback and comments, which greatly improved the quality of the manuscript. We thank M. Williams (BRLSI), M. Riley (CAMSM), P. Tomlinson (DORCM), I. Werneburg (GPIT), G. Garcia, F. Guy and P. Vignaud (LPP), O. Mateus (MG), S. Etches (MJML), M. Wilmsen (MMG), R. Allain (MNHN), B. Thuy and R. Weis (MNHNL), S. Maidment (NHMUK), T. Mörs (NRM), J. Dridi (ONM), E. Howlett and H. Ketchum (OUMNH), G. Wass (PETMG), K. Lauprasert (PRC), and E. Maxwell and R. Schoch (SMNS) for access to specimens, and V. Lamarque (MMT) for photographs of Seldsienean megistorhynchus. MMJ is currently supported by the Alexander von Humboldt Foundation (CAN 1218253 HFST-P) and her museum visits were funded by the Natural Sciences and Engineering Research Council of Canada (PGSD3-487581-2016), SYNTHESYS Project (FR-TAF-6577), the Small Grant Scheme (PA-SW201601), the Paleontological Society “Stephen Jay Gould Award” Student Research Grant, and Richard Owen Research Fund by the Palaeontographical Society. DF’s museum visits were funded by the Small Grant Scheme “2015 Wood Award” (PASW201402), Systematics Research Fund and Richard Owen Research Fund by the Palaeontographical Society. SLB and MTY were supported by Leverhulme Trust Research Project grant (RPG-2017-167). Finally, we sincerely thank J. Schwab and E. Amson for help and instruction in RStudio, C. Foth and K. Dexter for statistical discussion and S. Evers for discussion on turtle evolution. Open Access funding enabled and organized by Projekt DEAL.
Publisher Copyright:
© 2022 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd.
PY - 2022/11/18
Y1 - 2022/11/18
N2 - Throughout the Jurassic, a plethora of marine reptiles dominated ocean waters, including ichthyosaurs, plesiosaurs and thalattosuchian crocodylomorphs. These Jurassic ecosystems were characterized by high niche partitioning and spatial variation in dietary ecology. However, while the ecological diversity of many marine reptile lineages is well known, the overall ecological diversification of Teleosauroidea (one of the two major groups within thalattosuchian crocodylomorphs) has never been explored. Teleosauroids were previously deemed to have a morphologically conservative body plan; however, they were in actuality morphofunctionally more diverse than previously thought. Here we investigate the ecology and feeding specializations of teleosauroids, using morphological and functional cranio-dental characteristics. We assembled the most comprehensive dataset to date of teleosauroid taxa (approximately 20 species) and ran a series of principal component analyses (PC) to categorize them into various feeding ecomorphotypes based on 17 dental characteristics (38 specimens) and 16 functionally significant mandibular characters (18 specimens). The results were examined in conjunction with a comprehensive thalattosuchian phylogeny (153 taxa and 502 characters) to evaluate macroevolutionary patterns and significant ecological shifts. Machimosaurids display a well-developed ecological shift from: (1) slender, pointed tooth apices and an elongate gracile mandible; to (2) more robust, pointed teeth with a slightly deeper mandible; and finally, (3) rounded teeth and a deep-set, shortened mandible with enlarged musculature. Overall, there is limited mandibular functional variability in teleosaurids and machimosaurids, despite differing cranial morphologies and habitat preferences in certain taxa. This suggests a narrow feeding ecological divide between teleosaurids and machimosaurids. Resource partitioning was primarily related to snout and skull length as well as habitat; only twice did teleosauroids manage to make a major evolutionary leap to feed distinctly differently, with only the derived machimosaurines successfully radiating into new feeding ecologies.
AB - Throughout the Jurassic, a plethora of marine reptiles dominated ocean waters, including ichthyosaurs, plesiosaurs and thalattosuchian crocodylomorphs. These Jurassic ecosystems were characterized by high niche partitioning and spatial variation in dietary ecology. However, while the ecological diversity of many marine reptile lineages is well known, the overall ecological diversification of Teleosauroidea (one of the two major groups within thalattosuchian crocodylomorphs) has never been explored. Teleosauroids were previously deemed to have a morphologically conservative body plan; however, they were in actuality morphofunctionally more diverse than previously thought. Here we investigate the ecology and feeding specializations of teleosauroids, using morphological and functional cranio-dental characteristics. We assembled the most comprehensive dataset to date of teleosauroid taxa (approximately 20 species) and ran a series of principal component analyses (PC) to categorize them into various feeding ecomorphotypes based on 17 dental characteristics (38 specimens) and 16 functionally significant mandibular characters (18 specimens). The results were examined in conjunction with a comprehensive thalattosuchian phylogeny (153 taxa and 502 characters) to evaluate macroevolutionary patterns and significant ecological shifts. Machimosaurids display a well-developed ecological shift from: (1) slender, pointed tooth apices and an elongate gracile mandible; to (2) more robust, pointed teeth with a slightly deeper mandible; and finally, (3) rounded teeth and a deep-set, shortened mandible with enlarged musculature. Overall, there is limited mandibular functional variability in teleosaurids and machimosaurids, despite differing cranial morphologies and habitat preferences in certain taxa. This suggests a narrow feeding ecological divide between teleosaurids and machimosaurids. Resource partitioning was primarily related to snout and skull length as well as habitat; only twice did teleosauroids manage to make a major evolutionary leap to feed distinctly differently, with only the derived machimosaurines successfully radiating into new feeding ecologies.
U2 - 10.1002/ece3.9484
DO - 10.1002/ece3.9484
M3 - Article
C2 - 36415878
SN - 2045-7758
VL - 12
SP - e9484
JO - Ecology and Evolution
JF - Ecology and Evolution
IS - 11
M1 - e9484
ER -