On Hyperodapedon Gordoni
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Ischigualasto Formation. the Second Is a Sile- Diversity Or Abundance, but This Result Was Based on Only 19 of Saurid, Ignotosaurus Fragilis (Fig
This article was downloaded by: [University of Chicago Library] On: 10 October 2013, At: 10:52 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Journal of Vertebrate Paleontology Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/ujvp20 Vertebrate succession in the Ischigualasto Formation Ricardo N. Martínez a , Cecilia Apaldetti a b , Oscar A. Alcober a , Carina E. Colombi a b , Paul C. Sereno c , Eliana Fernandez a b , Paula Santi Malnis a b , Gustavo A. Correa a b & Diego Abelin a a Instituto y Museo de Ciencias Naturales, Universidad Nacional de San Juan , España 400 (norte), San Juan , Argentina , CP5400 b Consejo Nacional de Investigaciones Científicas y Técnicas , Buenos Aires , Argentina c Department of Organismal Biology and Anatomy, and Committee on Evolutionary Biology , University of Chicago , 1027 East 57th Street, Chicago , Illinois , 60637 , U.S.A. Published online: 08 Oct 2013. To cite this article: Ricardo N. Martínez , Cecilia Apaldetti , Oscar A. Alcober , Carina E. Colombi , Paul C. Sereno , Eliana Fernandez , Paula Santi Malnis , Gustavo A. Correa & Diego Abelin (2012) Vertebrate succession in the Ischigualasto Formation, Journal of Vertebrate Paleontology, 32:sup1, 10-30, DOI: 10.1080/02724634.2013.818546 To link to this article: http://dx.doi.org/10.1080/02724634.2013.818546 PLEASE SCROLL DOWN FOR ARTICLE Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content. -
Studies on Continental Late Triassic Tetrapod Biochronology. I. the Type Locality of Saturnalia Tupiniquim and the Faunal Succession in South Brazil
Journal of South American Earth Sciences 19 (2005) 205–218 www.elsevier.com/locate/jsames Studies on continental Late Triassic tetrapod biochronology. I. The type locality of Saturnalia tupiniquim and the faunal succession in south Brazil Max Cardoso Langer* Departamento de Biologia, FFCLRP, Universidade de Sa˜o Paulo (USP), Av. Bandeirantes 3900, 14040-901 Ribeira˜o Preto, SP, Brazil Received 1 November 2003; accepted 1 January 2005 Abstract Late Triassic deposits of the Parana´ Basin, Rio Grande do Sul, Brazil, encompass a single third-order, tetrapod-bearing sedimentary sequence that includes parts of the Alemoa Member (Santa Maria Formation) and the Caturrita Formation. A rich, diverse succession of terrestrial tetrapod communities is recorded in these sediments, which can be divided into at least three faunal associations. The stem- sauropodomorph Saturnalia tupiniquim was collected in the locality known as ‘Waldsanga’ near the city of Santa Maria. In that area, the deposits of the Alemoa Member yield the ‘Alemoa local fauna,’ which typifies the first association; includes the rhynchosaur Hyperodapedon, aetosaurs, and basal dinosaurs; and is coeval with the lower fauna of the Ischigualasto Formation, Bermejo Basin, NW Argentina. The second association is recorded in deposits of both the Alemoa Member and the Caturrita Formation, characterized by the rhynchosaur ‘Scaphonyx’ sulcognathus and the cynodont Exaeretodon, and correlated with the upper fauna of the Ischigualasto Formation. Various isolated outcrops of the Caturrita Formation yield tetrapod fossils that correspond to post-Ischigualastian faunas but might not belong to a single faunal association. The record of the dicynodont Jachaleria suggests correlations with the lower part of the Los Colorados Formation, NW Argentina, whereas remains of derived tritheledontid cynodonts indicate younger ages. -
The Early Evolution of Rhynchosaurs Butler, Richard; Montefeltro, Felipe; Ezcurra, Martin
University of Birmingham The early evolution of Rhynchosaurs Butler, Richard; Montefeltro, Felipe; Ezcurra, Martin DOI: 10.3389/fevo.2015.00142 License: Creative Commons: Attribution (CC BY) Document Version Publisher's PDF, also known as Version of record Citation for published version (Harvard): Butler, R, Montefeltro, F & Ezcurra, M 2016, 'The early evolution of Rhynchosaurs', Frontiers in Ecology and Evolution. https://doi.org/10.3389/fevo.2015.00142 Link to publication on Research at Birmingham portal Publisher Rights Statement: Frontiers is fully compliant with open access mandates, by publishing its articles under the Creative Commons Attribution licence (CC-BY). Funder mandates such as those by the Wellcome Trust (UK), National Institutes of Health (USA) and the Australian Research Council (Australia) are fully compatible with publishing in Frontiers. Authors retain copyright of their work and can deposit their publication in any repository. The work can be freely shared and adapted provided that appropriate credit is given and any changes specified. General rights Unless a licence is specified above, all rights (including copyright and moral rights) in this document are retained by the authors and/or the copyright holders. The express permission of the copyright holder must be obtained for any use of this material other than for purposes permitted by law. •Users may freely distribute the URL that is used to identify this publication. •Users may download and/or print one copy of the publication from the University of Birmingham research portal for the purpose of private study or non-commercial research. •User may use extracts from the document in line with the concept of ‘fair dealing’ under the Copyright, Designs and Patents Act 1988 (?) •Users may not further distribute the material nor use it for the purposes of commercial gain. -
Gondwana Vertebrate Faunas of India: Their Diversity and Intercontinental Relationships
438 Article 438 by Saswati Bandyopadhyay1* and Sanghamitra Ray2 Gondwana Vertebrate Faunas of India: Their Diversity and Intercontinental Relationships 1Geological Studies Unit, Indian Statistical Institute, 203 B. T. Road, Kolkata 700108, India; email: [email protected] 2Department of Geology and Geophysics, Indian Institute of Technology, Kharagpur 721302, India; email: [email protected] *Corresponding author (Received : 23/12/2018; Revised accepted : 11/09/2019) https://doi.org/10.18814/epiiugs/2020/020028 The twelve Gondwanan stratigraphic horizons of many extant lineages, producing highly diverse terrestrial vertebrates India have yielded varied vertebrate fossils. The oldest in the vacant niches created throughout the world due to the end- Permian extinction event. Diapsids diversified rapidly by the Middle fossil record is the Endothiodon-dominated multitaxic Triassic in to many communities of continental tetrapods, whereas Kundaram fauna, which correlates the Kundaram the non-mammalian synapsids became a minor components for the Formation with several other coeval Late Permian remainder of the Mesozoic Era. The Gondwana basins of peninsular horizons of South Africa, Zambia, Tanzania, India (Fig. 1A) aptly exemplify the diverse vertebrate faunas found Mozambique, Malawi, Madagascar and Brazil. The from the Late Palaeozoic and Mesozoic. During the last few decades much emphasis was given on explorations and excavations of Permian-Triassic transition in India is marked by vertebrate fossils in these basins which have yielded many new fossil distinct taxonomic shift and faunal characteristics and vertebrates, significant both in numbers and diversity of genera, and represented by small-sized holdover fauna of the providing information on their taphonomy, taxonomy, phylogeny, Early Triassic Panchet and Kamthi fauna. -
01 Oliveira & Pinheiro RBP V20 N2 COR.Indd
Rev. bras. paleontol. 20(2):155-162, Maio/Agosto 2017 © 2017 by the Sociedade Brasileira de Paleontologia doi: 10.4072/rbp.2017.2.01 ISOLATED ARCHOSAURIFORM TEETH FROM THE UPPER TRIASSIC CANDELÁRIA SEQUENCE (HYPERODAPEDON ASSEMBLAGE ZONE, SOUTHERN BRAZIL) TIANE MACEDO DE OLIVEIRA & FELIPE L. PINHEIRO Laboratório de Paleobiologia, Universidade Federal do Pampa, Campus São Gabriel, R. Aluízio Barros Macedo, BR 290, km 423, 97300-000, São Gabriel, RS, Brazil. [email protected], [email protected] ABSTRACT – We describe isolated teeth found in the locality “Sítio Piveta” (Hyperodapedon Assemblage Zone, Candelaria Sequence, Upper Triassic of the Paraná Basin). The material consists of five specimens, here classified into three different morphotypes. The morphotype I is characterized by pronounced elongation, rounded base and symmetry between lingual and labial surfaces. The morphotype II presents serrated mesial and distal edges, mesial denticles decreasing in size toward the base, distal denticles present until the base and asymmetry, with a flat lingual side and rounded labial side. The morphotype III, although similar to morphotype II, has a greater inclination of the posterior carinae. The conservative dental morphology in Archosauriformes makes difficult an accurate taxonomic assignment based only on isolated teeth. However, the specimens we present are attributable to “Rauisuchia” (morphotype II and III) and, possibly, Phytosauria (morphotype I). The putative presence of a phytosaur in the Carnian Hyperodapedon Assemblage Zone would have impact in the South American distribution of the group. The taxonomic assignments proposed herein contribute to the faunal composition of the Hyperodapedon Assemblage Zone, a critical unit on the study of the Upper Triassic radiation of archosaurs. -
Heptasuchus Clarki, from the ?Mid-Upper Triassic, Southeastern Big Horn Mountains, Central Wyoming (USA)
The osteology and phylogenetic position of the loricatan (Archosauria: Pseudosuchia) Heptasuchus clarki, from the ?Mid-Upper Triassic, southeastern Big Horn Mountains, Central Wyoming (USA) † Sterling J. Nesbitt1, John M. Zawiskie2,3, Robert M. Dawley4 1 Department of Geosciences, Virginia Tech, Blacksburg, VA, USA 2 Cranbrook Institute of Science, Bloomfield Hills, MI, USA 3 Department of Geology, Wayne State University, Detroit, MI, USA 4 Department of Biology, Ursinus College, Collegeville, PA, USA † Deceased author. ABSTRACT Loricatan pseudosuchians (known as “rauisuchians”) typically consist of poorly understood fragmentary remains known worldwide from the Middle Triassic to the end of the Triassic Period. Renewed interest and the discovery of more complete specimens recently revolutionized our understanding of the relationships of archosaurs, the origin of Crocodylomorpha, and the paleobiology of these animals. However, there are still few loricatans known from the Middle to early portion of the Late Triassic and the forms that occur during this time are largely known from southern Pangea or Europe. Heptasuchus clarki was the first formally recognized North American “rauisuchian” and was collected from a poorly sampled and disparately fossiliferous sequence of Triassic strata in North America. Exposed along the trend of the Casper Arch flanking the southeastern Big Horn Mountains, the type locality of Heptasuchus clarki occurs within a sequence of red beds above the Alcova Limestone and Crow Mountain formations within the Chugwater Group. The age of the type locality is poorly constrained to the Middle—early Late Triassic and is Submitted 17 June 2020 Accepted 14 September 2020 likely similar to or just older than that of the Popo Agie Formation assemblage from Published 27 October 2020 the western portion of Wyoming. -
Reptile Family Tree - Peters 2017 1112 Taxa, 231 Characters
Reptile Family Tree - Peters 2017 1112 taxa, 231 characters Note: This tree does not support DNA topologies over 100 Eldeceeon 1990.7.1 67 Eldeceeon holotype long phylogenetic distances. 100 91 Romeriscus Diplovertebron Certain dental traits are convergent and do not define clades. 85 67 Solenodonsaurus 100 Chroniosaurus 94 Chroniosaurus PIN3585/124 Chroniosuchus 58 94 Westlothiana Casineria 84 Brouffia 93 77 Coelostegus Cheirolepis Paleothyris Eusthenopteron 91 Hylonomus Gogonasus 78 66 Anthracodromeus 99 Osteolepis 91 Protorothyris MCZ1532 85 Protorothyris CM 8617 81 Pholidogaster Protorothyris MCZ 2149 97 Colosteus 87 80 Vaughnictis Elliotsmithia Apsisaurus Panderichthys 51 Tiktaalik 86 Aerosaurus Varanops Greererpeton 67 90 94 Varanodon 76 97 Koilops <50 Spathicephalus Varanosaurus FMNH PR 1760 Trimerorhachis 62 84 Varanosaurus BSPHM 1901 XV20 Archaeothyris 91 Dvinosaurus 89 Ophiacodon 91 Acroplous 67 <50 82 99 Batrachosuchus Haptodus 93 Gerrothorax 97 82 Secodontosaurus Neldasaurus 85 76 100 Dimetrodon 84 95 Trematosaurus 97 Sphenacodon 78 Metoposaurus Ianthodon 55 Rhineceps 85 Edaphosaurus 85 96 99 Parotosuchus 80 82 Ianthasaurus 91 Wantzosaurus Glaucosaurus Trematosaurus long rostrum Cutleria 99 Pederpes Stenocybus 95 Whatcheeria 62 94 Ossinodus IVPP V18117 Crassigyrinus 87 62 71 Kenyasaurus 100 Acanthostega 94 52 Deltaherpeton 82 Galechirus 90 MGUH-VP-8160 63 Ventastega 52 Suminia 100 Baphetes Venjukovia 65 97 83 Ichthyostega Megalocephalus Eodicynodon 80 94 60 Proterogyrinus 99 Sclerocephalus smns90055 100 Dicynodon 74 Eoherpeton -
Hyperodapedon Gordoni Further Observations Upon
Downloaded from http://jgslegacy.lyellcollection.org/ at University of Virginia on October 5, 2012 Quarterly Journal of the Geological Society Further Observations upon Hyperodapedon Gordoni. T. H. Huxley Quarterly Journal of the Geological Society 1887, v.43; p675-694. doi: 10.1144/GSL.JGS.1887.043.01-04.51 Email alerting click here to receive free service e-mail alerts when new articles cite this article Permission click here to seek permission request to re-use all or part of this article Subscribe click here to subscribe to Quarterly Journal of the Geological Society or the Lyell Collection Notes © The Geological Society of London 2012 Downloaded from http://jgslegacy.lyellcollection.org/ at University of Virginia on October 5, 2012 ON HYPERODAPEDON GORDONL 675 47. FcR~n~l~ O~S~RVAT][O~S upon ~EIYPERODAPEDOI~ GORDON][. By Prof. T. tI. HvxL~, F.R.S., F.G.S. (Read May 11, 1887.) [PLA~ES XXYL & XXVII.] IT is now twenty,nine years since, in describing those remains of Stagonolepis t~obertsoni from the Elgin Sandstones which enabled me to determine the reptilian nature and the crocodilian affinities of that supposed fish, I indicated the occurrence in the same beds of a Laeertilian reptile, to which I gave the name of Hyperodapedon Gordoni. I laid stress upon the " marked affinity with certain Triassic reptiles" (e. g. _Rhynchosaurus)of Hyperodapedon, and I said that these, "when taken together with the resemblance of Stagonolelois to Mesozoic Crocodilia," led me "to require the strongest stratigraphical proof before admitting the Palmozoic age of the beds in which it occurs ,' % Many Fellows of the Society will remember the prolonged dis- cussions which took place, in the course of the ensuing ten or twelve years, before the Mesozoic age of the reptiliferous sandstones of Elgin was universally admitted. -
Extant Taxa Stem Frogs Stem Turtles Stem Lepidosaurs Stem Squamates
Stem Taxa - Peters 2016 851 taxa, 228 characters 100 Eldeceeon 1990.7.1 91 Eldeceeon holotype 100 Romeriscus Ichthyostega Gephyrostegus watsoni Pederpes 85 Eryops 67 Solenodonsaurus 87 Proterogyrinus 100 Chroniosaurus Eoherpeton 94 72 Chroniosaurus PIN3585/124 98 Seymouria Chroniosuchus Kotlassia Stem 58 94 Westlothiana Utegenia Casineria 84 81 Amphibamus Brouffia 95 72 Cacops 93 77 Coelostegus Paleothyris 98 Doleserpeton 84 91 78 100 Gerobatrachus Hylonomus Rana Archosauromorphs Protorothyris MCZ1532 95 66 98 Adelospondylus 85 Protorothyris CM 8617 89 Brachydectes Protorothyris MCZ 2149 Eocaecilia 87 86 Microbrachis Vaughnictis Pantylus 80 89 75 94 Anthracodromeus Elliotsmithia 90 Utaherpeton 51 Apsisaurus Kirktonecta 95 90 86 Aerosaurus 96 Tuditanus 67 90 Varanops Stem Frogs 59 94 Eoserpeton Varanodon Diplocaulus Varanosaurus FMNH PR 1760 100 Sauropleura 62 84 Varanosaurus BSPHM 1901 XV20 88 Ptyonius 89 Archaeothyris 70 Scincosaurus Euryodus primus Ophiacodon 74 82 84 Micraroter Haptodus 91 Rhynchonkos 97 82 Secodontosaurus Batropetes 85 76 100 Dimetrodon 97 Sphenacodon Silvanerpeton Ianthodon 85 Edaphosaurus Gephyrostegeus bohemicus 99 Stem100 Reptiles 80 82 Ianthasaurus Glaucosaurus 94 Cutleria 100 Urumqia Bruktererpeton Stenocybus Stem Mammals 63 97 Thuringothyris MNG 7729 62 IVPP V18117 82 Thuringothyris MNG 10183 87 62 71 Kenyasaurus 82 Galechirus 52 Suminia Saurorictus Venjukovia 99 99 97 83 70 Cephalerpeton Opisthodontosaurus 94 Eodicynodon 80 98 Reiszorhinus 100 Dicynodon 75 Concordia KUVP 8702a Hipposaurus 100 98 96 Concordia -
Vertebrate Fauna from the Late Triassic Tiki Formation of India: New Finds and Their Biostratigraphic Implications
The Palaeobotanist 65(2016): 47–59 0031–0174/2016 Vertebrate fauna from the Late Triassic Tiki Formation of India: new finds and their biostratigraphic implications SANGHAMITRA RAY1*, MOHD. SHAFI BHAT1, DEBARATI MUKHERJEE2 AND P.M. DATTA3 1Department of Geology and Geophysics, Indian Institute of Technology, Kharagpur 721302, India. 2Geological Studies Unit, Indian Statistical Institute, 203 B.T. Road, Kolkata 700108, India. 3Greenwood Housing Cooperative Society Ltd., 315B Upen Banerjee Road, Kolkata 700060, India. *Corresponding author: [email protected] (Received 17 August, 2015; revised version accepted 06 February, 2016) ABSTRACT Ray S, Bhat MS, Mukherjee D & Datta PM 2016. Vertebrate fauna from the Late Triassic Tiki Formation of India: new finds and their biostratigraphic implications. The Palaeobotanist 65(1): 47–59. Recent work on the Tiki Formation has resulted in the collection of new and varied vertebrate micro–and megafossils, including a new bonebed containing low diversity, mono–dominant, multitaxic vertebrate accumulation where the rhynchosaur, Hyperodapedon tikiensis constitute the dominant component. This bonebed has also yielded a large traversodontid cynodont Ruberodon roychowdhurii. In addition, there are several diagnostic postcrania such as vertebrae and incomplete limb bones belonging to a basal saurischian dinosaur. Systematic exploration and collection has yielded numerous isolated teeth and postcrania of small vertebrates such as different types of freshwater sharks, bony fishes, archosauriforms, lepidosauromorphs, cynodonts and other reptiles. Based on its fossil flora and fauna, the Tiki Formation is globally correlated with other coeval horizons such as the lower member of the Maleri Formation of the Pranhita–Godavari basin, the upper part of the Santa Maria Formation of Brazil, the Camp Springs and lower Tecovas formations of the Chinle Group, USA. -
Reptile Family Tree Peters 2021 1909 Taxa, 235 Characters
Turinia Enoplus Chondrichtyes Jagorina Gemuendina Manta Chordata Loganellia Ginglymostoma Rhincodon Branchiostoma Tristychius Pikaia Tetronarce = Torpedo Palaeospondylus Craniata Aquilolamna Tamiobatis Myxine Sphyrna Metaspriggina Squalus Arandaspis Pristis Poraspis Rhinobatos Drepanaspis Cladoselache Pteromyzon adult Promissum Chlamydoselachus Pteromyzon hatchling Aetobatus Jamoytius Squatina Birkenia Heterodontus Euphanerops Iniopteryx Drepanolepis Helodus Callorhinchus Haikouichthys Scaporhynchus Belantsea Squaloraja Hemicyclaspis Chimaera Dunyu CMNH 9280 Mitsukurina Rhinochimaera Tanyrhinichthys Isurus Debeerius Thelodus GLAHM–V8304 Polyodon hatchling Cetorhinus Acipenser Yanosteus Oxynotus Bandringa PF8442 Pseudoscaphirhynchus Isistius Polyodon adult Daliatus Bandringa PF5686 Gnathostomata Megachasma Xenacanthus Dracopristis Akmonistion Ferromirum Strongylosteus Ozarcus Falcatus Reptile Family Tree Chondrosteus Hybodus fraasi Hybodus basanus Pucapampella Osteichthyes Orodus Peters 2021 1943 taxa, 235 characters Gregorius Harpagofututor Leptolepis Edestus Prohalecites Gymnothorax funebris Doliodus Gymnothorax afer Malacosteus Eurypharynx Amblyopsis Lepidogalaxias Typhlichthys Anableps Kryptoglanis Phractolaemus Homalacanthus Acanthodes Electrophorus Cromeria Triazeugacanthus Gymnotus Gorgasia Pholidophorus Calamopleurus Chauliodus Bonnerichthys Dactylopterus Chiasmodon Osteoglossum Sauropsis Synodus Ohmdenia Amia Trachinocephalus BRSLI M1332 Watsonulus Anoplogaster Pachycormus Parasemionotus Aenigmachanna Protosphyraena Channa Aspidorhynchus -
(GIS) Study of Triassic Vertebrate Biochronology
Geol. Mag. 142 (4), 2005, pp. 327–354. c 2005 Cambridge University Press 327 doi:10.1017/S001675680500083X Printed in the United Kingdom A Geographical Information System (GIS) study of Triassic vertebrate biochronology ∗ E. J. RAYFIELD ,P.M.BARRETT†,R.A.MCDONNELL‡ & K. J. WILLIS‡ ∗Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EQ, UK †Department of Palaeontology, The Natural History Museum, Cromwell Road, London SW7 5BD, UK ‡School of Geography and the Environment, University of Oxford, Mansfield Road, Oxford OX1 3TB, UK (Received 17 June 2004; accepted 10 February 2005) Abstract – Geographical Information Systems (GIS) have been applied extensively to analyse spatial data relating to varied environmental issues, but have not so far been used to address biostratigraphical or macroevolutionary questions over extended spatial and temporal scales. Here, we use GIS techniques to test the stability, validity and utility of proposed Middle and Late Triassic ‘Land Vertebrate Faunachrons’ (LVFs), a global biostratigraphical framework based upon terrestrial/freshwater tetrapod occurrences. A database of tetrapod and megafloral localities was constructed for North America and Western Europe that also incorporated information on relevant palaeoenvironmental variables. This database was subjected to various spatial analysis techniques. Our GIS analysis found support at a global level for Eocyclotosaurus as an Anisian index taxon and probably Aetosaurus as a Norian indicator. Other tetrapod taxa are useful biostratigraphical/biochronological markers on a regional basis, such as Longosuchus and Doswellia for Late Carnian time. Other potential index fossils are hampered, however, by taxonomic instability (Mastodonsaurus, Metoposaurus, Typothorax, Paleorhinus, Pseudopalatus, Redondasaurus, Redondasuchus) and/or are not clearly restricted in temporal distribution (Paleorhinus, Angistorhinus, Stagonolepis, Metoposaurus and Rutiodon).