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  • Notas Sobre Spinosauridae (Theropoda, Dinosauria) Notes on Spinosauridae (Theropoda, Dinosauria)

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    Anuário do Instituto de Geociências - UFRJ ISSN 0101-9759 Vol. 28-1 / 2005 p. 158-173 Notas Sobre Spinosauridae (Theropoda, Dinosauria) Notes on Spinosauridae (Theropoda, Dinosauria) Elaine Batista Machado1 & Alexander Wilhelm Armin Kellner2 1Setor de Paleovertebrados, Museu Nacional/UFRJ Quinta da Boa Vista s/n., São Cristóvão, Rio de Janeiro - RJ, CEP: 20940-040 e-mail: [email protected] 2Setor de Paleovertebrados, Museu Nacional/UFRJ Quinta da Boa Vista s/n., São Cristóvão, Rio de Janeiro - RJ, CEP: 20940-040 email: [email protected] Recebido: 08/11/2005 Aprovado: 19/11/2005 Resumo Os espinossaurídeos são encontrados na África, Europa, Ásia e Brasil em depósitos com idade variando do Jurássico Superior até o Cretáceo Superior, tendo sido descritos até a presente data oito espécies. Apesar desta grande distribuição temporal e geográfica, pouco se sabe sobre este grupo de dinossauros uma vez que a maior parte dos espécimes são incompletos. O clado Spinosauridae é dividido em Baryonychinae (Suchomimus + Baryonyx + Cristatosaurus) e Spinosaurinae (Spinosaurus+ Angaturama + Irritator). Apenas na África representantes destes dois clados foram encontrados. Uma possível explicação para a distribuição dos espinossaurídeos seria a dispersão de formas relacionadas a Baryonyx (o mais primitivo membro do grupo) da Europa para a África, onde surgiram os Spinosaurinae que posteriormente se distribuíram para a América do Sul. Palavras-chave: Dinosauria, Theropoda, Spinosauridae Abstract Spinosaur remains were collected in Africa, Europa, Asia and Brazil, coming from deposits with ages ranging from the Late Jurassic to the Late Cretaceous. Although having a wide distribution - both geographically and temporally - little is actually known about the group since most specimens are incomplete.
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    Vertebrate Anatomy Morphology Palaeontology 6:68-72 68 ISSN 2292-1389 Rebuttal of McFeeters, Ryan and Cullen, 2018, ‘Positional variation in pedal unguals of North American ornithomimids (Dinosauria, Theropoda): A Response to Brownstein (2017)’ Chase Doran Brownstein Stamford Museum, 39 Scofieldtown Road, Stamford, CT 06903, USA; [email protected] Abstract: The Arundel Clay of Maryland is among the only Early Cretaceous terrestrial units known from eastern North America. Research on some theropod dinosaur bones from this layer has indicated the presence of two ornithomimosaur taxa in the assemblage. However, a recent paper discussed issues with the definite assignment of any of these unguals to Ornithomimosauria and suggested that morphological differences originally interpreted to be indicative of the presence of two ornithomimosaurs could be explained by positional variation. Here, I show that substantial evidence persists for the presence of two ornithomimosaurs in the Arundel Clay assemblage, even considering the recent description of positional variation in ornithomimosaur pedal unguals. Furthermore, the argument against the confident assignment of these unguals to ornithomimosaurs is shown to be based on oversimplified comparisons that do not take into account the combination of features in the Arundel specimens that allow for their assignment to that clade. Although several small points made in the initial paper describing the Arundel specimens are incorrect or unsubstantiated, the differences between the Maryland unguals are outside the spectrum of positional variation and are indicative of the presence of two ornithomimosaurs in the Arundel Clay assemblage. The Arundel Clay of Maryland is an Aptian unit (e.g., Lipka major acts in that paper: (1) the confident assignment of the et al.
  • Lyons SCIENCE 2021 the Influence of Juvenile Dinosaurs SUPPL.Pdf

    Lyons SCIENCE 2021 the Influence of Juvenile Dinosaurs SUPPL.Pdf

    science.sciencemag.org/content/371/6532/941/suppl/DC1 Supplementary Materials for The influence of juvenile dinosaurs on community structure and diversity Katlin Schroeder*, S. Kathleen Lyons, Felisa A. Smith *Corresponding author. Email: [email protected] Published 26 February 2021, Science 371, 941 (2021) DOI: 10.1126/science.abd9220 This PDF file includes: Materials and Methods Supplementary Text Figs. S1 and S2 Tables S1 to S7 References Other Supplementary Material for this manuscript includes the following: (available at science.sciencemag.org/content/371/6532/941/suppl/DC1) MDAR Reproducibility Checklist (PDF) Materials and Methods Data Dinosaur assemblages were identified by downloading all vertebrate occurrences known to species or genus level between 200Ma and 65MA from the Paleobiology Database (PaleoDB 30 https://paleobiodb.org/#/ download 6 August, 2018). Using associated depositional environment and taxonomic information, the vertebrate database was limited to only terrestrial organisms, excluding amphibians, pseudosuchians, champsosaurs and ichnotaxa. Taxa present in formations were confirmed against the most recent available literature, as of November, 2020. Synonymous taxa or otherwise duplicated taxa were removed. Taxa that could not be identified to genus level 35 were included as “Taxon X”. GPS locality data for all formations between 200MA and 65MA was downloaded from PaleoDB to create a minimally convex polygon for each possible formation. Any attempt to recreate local assemblages must include all potentially interacting species, while excluding those that would have been separated by either space or time. We argue it is 40 acceptable to substitute formation for home range in the case of non-avian dinosaurs, as range increases with body size.