Sauropodomorpha Saurisquia
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The Origin and Early Evolution of Dinosaurs
Biol. Rev. (2010), 85, pp. 55–110. 55 doi:10.1111/j.1469-185X.2009.00094.x The origin and early evolution of dinosaurs Max C. Langer1∗,MartinD.Ezcurra2, Jonathas S. Bittencourt1 and Fernando E. Novas2,3 1Departamento de Biologia, FFCLRP, Universidade de S˜ao Paulo; Av. Bandeirantes 3900, Ribeir˜ao Preto-SP, Brazil 2Laboratorio de Anatomia Comparada y Evoluci´on de los Vertebrados, Museo Argentino de Ciencias Naturales ‘‘Bernardino Rivadavia’’, Avda. Angel Gallardo 470, Cdad. de Buenos Aires, Argentina 3CONICET (Consejo Nacional de Investigaciones Cient´ıficas y T´ecnicas); Avda. Rivadavia 1917 - Cdad. de Buenos Aires, Argentina (Received 28 November 2008; revised 09 July 2009; accepted 14 July 2009) ABSTRACT The oldest unequivocal records of Dinosauria were unearthed from Late Triassic rocks (approximately 230 Ma) accumulated over extensional rift basins in southwestern Pangea. The better known of these are Herrerasaurus ischigualastensis, Pisanosaurus mertii, Eoraptor lunensis,andPanphagia protos from the Ischigualasto Formation, Argentina, and Staurikosaurus pricei and Saturnalia tupiniquim from the Santa Maria Formation, Brazil. No uncontroversial dinosaur body fossils are known from older strata, but the Middle Triassic origin of the lineage may be inferred from both the footprint record and its sister-group relation to Ladinian basal dinosauromorphs. These include the typical Marasuchus lilloensis, more basal forms such as Lagerpeton and Dromomeron, as well as silesaurids: a possibly monophyletic group composed of Mid-Late Triassic forms that may represent immediate sister taxa to dinosaurs. The first phylogenetic definition to fit the current understanding of Dinosauria as a node-based taxon solely composed of mutually exclusive Saurischia and Ornithischia was given as ‘‘all descendants of the most recent common ancestor of birds and Triceratops’’. -
The Sauropodomorph Biostratigraphy of the Elliot Formation of Southern Africa: Tracking the Evolution of Sauropodomorpha Across the Triassic–Jurassic Boundary
Editors' choice The sauropodomorph biostratigraphy of the Elliot Formation of southern Africa: Tracking the evolution of Sauropodomorpha across the Triassic–Jurassic boundary BLAIR W. MCPHEE, EMESE M. BORDY, LARA SCISCIO, and JONAH N. CHOINIERE McPhee, B.W., Bordy, E.M., Sciscio, L., and Choiniere, J.N. 2017. The sauropodomorph biostratigraphy of the Elliot Formation of southern Africa: Tracking the evolution of Sauropodomorpha across the Triassic–Jurassic boundary. Acta Palaeontologica Polonica 62 (3): 441–465. The latest Triassic is notable for coinciding with the dramatic decline of many previously dominant groups, followed by the rapid radiation of Dinosauria in the Early Jurassic. Among the most common terrestrial vertebrates from this time, sauropodomorph dinosaurs provide an important insight into the changing dynamics of the biota across the Triassic–Jurassic boundary. The Elliot Formation of South Africa and Lesotho preserves the richest assemblage of sauropodomorphs known from this age, and is a key index assemblage for biostratigraphic correlations with other simi- larly-aged global terrestrial deposits. Past assessments of Elliot Formation biostratigraphy were hampered by an overly simplistic biozonation scheme which divided it into a lower “Euskelosaurus” Range Zone and an upper Massospondylus Range Zone. Here we revise the zonation of the Elliot Formation by: (i) synthesizing the last three decades’ worth of fossil discoveries, taxonomic revision, and lithostratigraphic investigation; and (ii) systematically reappraising the strati- graphic provenance of important fossil locations. We then use our revised stratigraphic information in conjunction with phylogenetic character data to assess morphological disparity between Late Triassic and Early Jurassic sauropodomorph taxa. Our results demonstrate that the Early Jurassic upper Elliot Formation is considerably more taxonomically and morphologically diverse than previously thought. -
A Re-Evaluation of the Enigmatic Dinosauriform Caseosaurus Crosbyensis from the Late Triassic of Texas, USA and Its Implications for Early Dinosaur Evolution
A re-evaluation of the enigmatic dinosauriform Caseosaurus crosbyensis from the Late Triassic of Texas, USA and its implications for early dinosaur evolution MATTHEW G. BARON and MEGAN E. WILLIAMS Baron, M.G. and Williams, M.E. 2018. A re-evaluation of the enigmatic dinosauriform Caseosaurus crosbyensis from the Late Triassic of Texas, USA and its implications for early dinosaur evolution. Acta Palaeontologica Polonica 63 (1): 129–145. The holotype specimen of the Late Triassic dinosauriform Caseosaurus crosbyensis is redescribed and evaluated phylogenetically for the first time, providing new anatomical information and data on the earliest dinosaurs and their evolution within the dinosauromorph lineage. Historically, Caseosaurus crosbyensis has been considered to represent an early saurischian dinosaur, and often a herrerasaur. More recent work on Triassic dinosaurs has cast doubt over its supposed dinosaurian affinities and uncertainty about particular features in the holotype and only known specimen has led to the species being regarded as a dinosauriform of indeterminate position. Here, we present a new diagnosis for Caseosaurus crosbyensis and refer additional material to the taxon—a partial right ilium from Snyder Quarry. Our com- parisons and phylogenetic analyses suggest that Caseosaurus crosbyensis belongs in a clade with herrerasaurs and that this clade is the sister taxon of Dinosauria, rather than positioned within it. This result, along with other recent analyses of early dinosaurs, pulls apart what remains of the “traditional” group of dinosaurs collectively termed saurischians into a polyphyletic assemblage and implies that Dinosauria should be regarded as composed exclusively of Ornithoscelida (Ornithischia + Theropoda) and Sauropodomorpha. In addition, our analysis recovers the enigmatic European taxon Saltopus elginensis among herrerasaurs for the first time. -
The Anatomy and Phylogenetic Relationships of Antetonitrus Ingenipes (Sauropodiformes, Dinosauria): Implications for the Origins of Sauropoda
THE ANATOMY AND PHYLOGENETIC RELATIONSHIPS OF ANTETONITRUS INGENIPES (SAUROPODIFORMES, DINOSAURIA): IMPLICATIONS FOR THE ORIGINS OF SAUROPODA Blair McPhee A dissertation submitted to the Faculty of Science, University of the Witwatersrand, in partial fulfilment of the requirements for the degree of Master of Science. Johannesburg, 2013 i ii ABSTRACT A thorough description and cladistic analysis of the Antetonitrus ingenipes type material sheds further light on the stepwise acquisition of sauropodan traits just prior to the Triassic/Jurassic boundary. Although the forelimb of Antetonitrus and other closely related sauropododomorph taxa retains the plesiomorphic morphology typical of a mobile grasping structure, the changes in the weight-bearing dynamics of both the musculature and the architecture of the hindlimb document the progressive shift towards a sauropodan form of graviportal locomotion. Nonetheless, the presence of hypertrophied muscle attachment sites in Antetonitrus suggests the retention of an intermediary form of facultative bipedality. The term Sauropodiformes is adopted here and given a novel definition intended to capture those transitional sauropodomorph taxa occupying a contiguous position on the pectinate line towards Sauropoda. The early record of sauropod diversification and evolution is re- examined in light of the paraphyletic consensus that has emerged regarding the ‘Prosauropoda’ in recent years. iii ACKNOWLEDGEMENTS First, I would like to express sincere gratitude to Adam Yates for providing me with the opportunity to do ‘real’ palaeontology, and also for gladly sharing his considerable knowledge on sauropodomorph osteology and phylogenetics. This project would not have been possible without the continued (and continual) support (both emotionally and financially) of my parents, Alf and Glenda McPhee – Thank you. -
104Ornithodiraphyl
Millions of Years Ago 252.3 247.2 235.0 201.5 175.6 161.2 145.5 99.6 65.5 Triassic Jurassic Cretaceous Early Middle Late Early Middle Late Early Late Euparkeria Crurotarsi ? Scleromochlus ? Archosauria Pterosauria Lagerpetidae Ornithodira Marasuchus Genasauria Dinosauromorpha Silesauridae Neornithsichia Thyreophora Ornithischia Eocursor (esp. Dinosauria) et al. (2011), Yates (2007) Yates et al. (2011), Nesbitt etal.(2009), Sues (2007), Martinezet al.(2011), Irmis etal. Ezcurra (2006), EzcurraandBrusatte (2011), Phylogeny after Brusatteetal.(2010), Butleretal.(2007), Heterodontosauridae Pisanosaurus Dinosauria Ornithodira Sauropodomorpha Herrerasauria Saurischia Eodromeus Theropoda Daemonosaurus Tawa Neotheropoda Millions of Years Ago 253.0 247.2 235.0 201.5 175.6 161.2 145.5 99.6 65.5 Triassic Jurassic Cretaceous Early Middle Late Early Middle Late Early Late (2009), Norman et al. (2004), Thompson etal. (2011) (2009), Norman etal. (2004), Phylogeny afterButler etal. (2007a,b), Carpenter (2001),Galton &Upchurch (2004), Maidment etal.(2008), Mateus etal. Cerapoda Ornithopoda Eocursor Marginocephalia Neornithischia Othnielosaurus Genasauria (esp. Thyreophora) Genasauria (esp. Hexinlusaurus Stormbergia Genasauria Lesothosaurus Scutellosaurus Thyreophora Scelidosaurus Stegosauridae Stegosaurinae Dacentrurinae Stegosauria Kentrosaurus Tuojiangosaurus Huayangosauridae Gigantspinosaurus Eurypoda Tianchiasaurus Ankylosauria Nodosauridae Ankylosauridae Millions of Years Ago 253.0 247.2 235.0 201.5 175.6 161.2 145.5 99.6 65.5 Triassic Jurassic Cretaceous -
Skull Remains of the Dinosaur Saturnalia Tupiniquim (Late Triassic, Brazil): with Comments on the Early Evolution of Sauropodomorph Feeding Behaviour
RESEARCH ARTICLE Skull remains of the dinosaur Saturnalia tupiniquim (Late Triassic, Brazil): With comments on the early evolution of sauropodomorph feeding behaviour 1 2 1 Mario BronzatiID *, Rodrigo T. MuÈ llerID , Max C. Langer * 1 LaboratoÂrio de Paleontologia, Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de a1111111111 São Paulo, Ribeirão Preto, São Paulo, Brazil, 2 Centro de Apoio à Pesquisa PaleontoloÂgica, Universidade Federal de Santa Maria, Santa Maria, Rio Grande do Sul, Brazil a1111111111 a1111111111 * [email protected] (MB); [email protected] (MCL) a1111111111 a1111111111 Abstract Saturnalia tupiniquim is a sauropodomorph dinosaur from the Late Triassic (Carnian±c. 233 OPEN ACCESS Ma) Santa Maria Formation of Brazil. Due to its phylogenetic position and age, it is important for studies focusing on the early evolution of both dinosaurs and sauropodomorphs. The Citation: Bronzati M, MuÈller RT, Langer MC (2019) Skull remains of the dinosaur Saturnalia tupiniquim osteology of Saturnalia has been described in a series of papers, but its cranial anatomy (Late Triassic, Brazil): With comments on the early remains mostly unknown. Here, we describe the skull bones of one of its paratypes (only in evolution of sauropodomorph feeding behaviour. the type-series to possess such remains) based on CT Scan data. The newly described ele- PLoS ONE 14(9): e0221387. https://doi.org/ ments allowed estimating the cranial length of Saturnalia and provide additional support for 10.1371/journal.pone.0221387 the presence of a reduced skull (i.e. two thirds of the femoral length) in this taxon, as typical Editor: JuÈrgen Kriwet, University of Vienna, of later sauropodomorphs. -
Evolution of the Caudal Vertebral Series in Macronarian Sauropod Dinosaurs: Morphofunctional and Phylogenetic Implications
Evolution of the Caudal Vertebral Series in Macronarian Sauropod Dinosaurs: Morphofunctional and Phylogenetic Implications A Thesis Submitted to the Faculty of Drexel University By Lucio Manuel Ibiricu In partial fulfillment of the Requirements for the degree of Doctor of Philosophy October 2010 © Copyright 2010 Lucio Manuel Ibiricu. All Rights Reserved ii DEDICATION To the people who trusted me and my grandfather (Manolo) iii ACKNOWLEDGMENTS First of all, I want to thank my advisor, Dr. Lacovara, for several things: for admitting me in the program, for supporting me constantly, especially at the beginning of my experience in the United States and for exposing me to ―big‖ people in Paleontology. Ken gave me the opportunity to work and learn; I will always be grateful to him. I also thank Dr. Spotila, the head of my committee, for always supporting me and for helping in the organization, always very important during the PhD. I really appreciate it. In addition, I want to thank Dr. Dodson for accepting to be part of my committee. His presence is a privilege to me and it is an honor to say that he was part of my PhD committee. I would like to express my gratitude to Dr. Gallagher. He taught me the majority of my first courses at Drexel and I always learned a lot from him. Also, my first TA was under his supervision; therefore, I want to thank him for all the support he gave me both as student and as a TA. Likewise, I would like to thank Dr. Kilham, because her presence in my committee pushed me to learn more about ecology, which helped me integrate dinosaurs and their environment. -
34º Jornadas Argentinas De Paleontología De Vertebrados
34º JORNADAS ARGENTINAS DE PALEONTOLOGÍA DE VERTEBRADOS 34º JAPV 2021 - Mendoza ii 34º JAPV 2021 - Mendoza 34º JORNADAS ARGENTINAS DE PALEONTOLOGÍA DE VERTEBRADOS LIBRO DE RESÚMENES 26, 27 y 28 de mayo 2021 Instituciones Organizadoras Instituto Argentino de Nivología, Glaciología y Ciencias Ambientales (IANIGLA), Museo de Historia Natural de San Rafael (MHNSR) y Museo de Ciencias Naturales y Antropológicas “Juan Cornelio Moyano” (MCNAM). Auspiciantes Universidad Nacional de Cuyo (UNCUYO), Asociación Paleontológica Argentina (APA), Dirección de Patrimonio Cultural y Museos, Ministerio de Cultura y Turismo, Mendoza. Auspiciantes Simposio de Patrimonio Paleontológico ICOM Argentina y Fundación Azara. Financiadores Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET) y Fundación Balseiro. iii 34º JAPV 2021 - Mendoza iv 34º JAPV 2021 - Mendoza COMITÉ ORGANIZADOR: Dra. Cecilia Benavente (Coordinadora), Sr. Jorge L. Blanco, Dr. Alberto Boscaini, Sr. Marcelo Bourguet, Dra. Evelyn Luz Bustos, Dra. Esperanza Cerdeño (Coordinadora general), Dr. Marcelo de la Fuente (Coordinador general), Lic. Susana Devincenzi, Dr. Marcos Fernández García, Dra. Analía M. Forasiepi (Coordinadora referente), MSc. Charlene Gaillard, MSc. Pablo González Ruíz, Lic. Silvina Lassa, Dra. Adriana C. Mancuso (Coordinadora general), Dr. Ignacio Maniel, Lic. Alejandra Moschetti, Dr. Tomás Pedernera, Dra. Elena Previtera, Dr. François Pujos, MSc. Cristo O. Romano Muñoz (Coordinador) y Sr. Cristian Sancho. COMITÉ EDITOR: Dr. Alberto Boscaini, Dra. Esperanza Cerdeño (Coordinadora), Dr. Marcos Fernández García, Dr. Marcelo de la Fuente, Dr. Ignacio Maniel, Dra. Elena Previtera, Dr. François Pujos y MSc. Cristo O. Romano Muñoz. COMITÉ CIENTÍFICO EXTERNO: Dr. Fernando Abdala, Dra. Alejandra Abello, Dra. Andrea Arcucci, Dra. Susana Bargo, Dra. Paula Bona, Lic. Mariano Bond, Dr. -
What Are Dinosaurs?
Tote Hughes, 140819 [email protected] Dinosaurs 1/20 What Are Dinosaurs? The following are not dinosaurs∗: • Things that aren’t organisms—There is no rock that is a dinosaur. • Things that existed before the Triassic period† • Pterosaurs The following are dinosaurs: • Birds (Aves) The following contain dinosaurs: • Archosaurs (X.Archosauria) • Reptiles (Reptilia) Dinosaur Overview A discussion of the important dinosaur clades. Dinosaurs are divided into two main groups: the eusaurischians‡ and ornithischians. Eusaurischians • Sauropods – Apatasaurus: diplodocoidean – Barosaurus: diplodocoidean – Brachiosaurus: macronarian – Diplodocus: diplodocoidean • Theropods – Allosaurus: carnosaurian – Archaeopteryx: maniraptor – Giganotosaurus: carnosaurian – Megalosaurus: megalosaurid – Spinosaurus: megalosaurid – Tyrannosaurus: tyrannosauroid – Velociraptor: maniraptor ∗See the Dinosaur Encyclopedia section for details on terms. †See Appendix: Time for details on geological time. ‡These are commonly called saurischians, but since almost every interesting saurischian is actually in the subclade X.Eusaurischia, I’ve taken the liberty of breaking the standard. I hope you will grow to understand and accept my decision. 1/20 Tote Hughes, 140819 [email protected] Dinosaurs 2/20 Ornithischians • Eurypodans (thyreophor) – Ankylosaurus: ankylosaurian – Stegosaurus: stegosaurian • Marginocephalians (cerapod) – Pachycephalosaurus: pachycephalosaurian – Triceratops: ceratopsian • Ornithopods (cerapod) – Hadrosaurus: hadrosauriform – Iguanodon: hadrosauriform -
Craniodental Functional Evolution in Sauropodomorph Dinosaurs
Paleobiology, 43(3), 2017, pp. 435–462 DOI: 10.1017/pab.2017.4 Craniodental functional evolution in sauropodomorph dinosaurs David J. Button, Paul M. Barrett, and Emily J. Rayfield Abstract.—Sauropodomorpha included the largest known terrestrial vertebrates and was the first dinosaur clade to achieve a global distribution. This success is associated with their early adoption of herbivory, and sauropod gigantism has been hypothesized to be a specialization for bulk feeding and obligate high-fiber herbivory. Here, we apply a combination of biomechanical character analysis and comparative phylogenetic methods with the aim of quantifying the evolutionary mechanics of the saur- opodomorph feeding apparatus. We test for the role of convergence to common feeding function and divergence toward functional optima across sauropodomorph evolution, quantify the rate of evolution for functional characters, and test for coincident evolutionary rate shifts in craniodental functional characters and body mass. Results identify a functional shift toward increased cranial robustness, increased bite force, and the onset of static occlusion at the base of the Sauropoda, consistent with a shift toward bulk feeding. Trends toward similarity in functional characters are observed in Diplodocoidea and Titanosauriformes. However, diplodocids and titanosaurs retain significant craniodental functional differences, and evidence for convergent adoption of a common “adaptive zone” between them is weak. Modeling of craniodental character and body-mass evolution demonstrates that these functional shifts were not correlated with evolutionary rate shifts. Instead, a significant correlation between body mass and characters related to bite force and cranial robustness suggests a correlated-progression evolutionary mode, with positive-feedback loops between body mass and dietary specializations fueling sauropod gigantism. -
Craniodental Functional Evolution in Sauropodomorph Dinosaurs
Button, D. J. , Barrett, P. M., & Rayfield, E. J. (2017). Craniodental functional evolution in sauropodomorph dinosaurs. Paleobiology, 43(3), 435-462. https://doi.org/10.1017/pab.2017.4 Publisher's PDF, also known as Version of record License (if available): CC BY Link to published version (if available): 10.1017/pab.2017.4 Link to publication record in Explore Bristol Research PDF-document This is the final published version of the article (version of record). It first appeared online via Cambridge University Press at https://doi.org/10.1017/pab.2017.4 . Please refer to any applicable terms of use of the publisher. University of Bristol - Explore Bristol Research General rights This document is made available in accordance with publisher policies. Please cite only the published version using the reference above. Full terms of use are available: http://www.bristol.ac.uk/red/research-policy/pure/user-guides/ebr-terms/ Paleobiology, 43(3), 2017, pp. 435–462 DOI: 10.1017/pab.2017.4 Craniodental functional evolution in sauropodomorph dinosaurs David J. Button, Paul M. Barrett, and Emily J. Rayfield Abstract.—Sauropodomorpha included the largest known terrestrial vertebrates and was the first dinosaur clade to achieve a global distribution. This success is associated with their early adoption of herbivory, and sauropod gigantism has been hypothesized to be a specialization for bulk feeding and obligate high-fiber herbivory. Here, we apply a combination of biomechanical character analysis and comparative phylogenetic methods with the aim of quantifying the evolutionary mechanics of the saur- opodomorph feeding apparatus. We test for the role of convergence to common feeding function and divergence toward functional optima across sauropodomorph evolution, quantify the rate of evolution for functional characters, and test for coincident evolutionary rate shifts in craniodental functional characters and body mass. -
Xxvi Jornadas...Qxd
AMEGHINIANA Revista de la Asociación Paleontológica Argentina RESÚMENES TOMO 46 Número 4 BUENOS AIRES REPÚBLICA ARGENTINA 2009 Se deja constancia que el presente suplemento se halla desprovisto de validez para propósitos nomenclaturales Disclaimer: this supplement is not deemed to be valid for nomenclatural purposes El Comité Editor de la Asociación Paleontológica Argentina deja constancia que solamente se incluyen en este Suplemento los resúmenes enviados por los organizadores de las diferentes reuniones. AMEGHINIANA 46 (4) Suplemento, 2009-RESÚMENES XXIV JORNADAS ARGENTINAS DE PALEONTOLOGÍA DE VERTEBRADOS RESÚMENES 4 al 7 de mayo de 2009 Museo de Historia Natural de San Rafael (MHNSR), San Rafael, Mendoza COMISIÓN ORGANIZADORA Presidente Marcelo S. de la Fuente (MHNSR) Secretarias Analía Forasiepi (MHNSR) Juliana Sterli (MHNSR) Vocales Miriam Ayala (MHNSR) René Biglione (DGE-Mendoza) Sergio Dieguez (CNEA) Gladys García (Universidad Champagnat) Miguel Giardina (MHNSR) Adolfo Gil (MHNSR) Gustavo Neme (MHNSR) Clara Otaola (MHNSR) Nuria Sugrañes (MHNSR) Financiado por ANPCyT, CONICET y Fondo Provincial de la Cultura de la Pcia. de Mendoza. Auspiciado por Asociación Paleontológica Argentina, Museo de Historia Natural de San Rafael y Municipalidad de San Rafael (Mendoza). AMEGHINIANA 46 (4) Sumplemento, 2009-RESÚMENES 4R CONFERENCIAS Origen de la ictiofauna marina y continental de América del Sur Austral A.L. CIONE1 La ictiofauna neotropical continental es la más rica en especies del mundo. Su mayor riqueza se localiza en las áreas intertropi- cales, un paralelo de lo que sucede con otros organismos. Se calcula que pueden existir 8.000 especies de peces continentales, un cuarto de la totalidad de los conocidos en todo el mundo en ambiente marino o continental.