Short Review of the Present Knowledge of the Sauropoda
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CPY Document
v^ Official Journal of the Biology Unit of the American Topical Association 10 Vol. 40(4) DINOSAURS ON STAMPS by Michael K. Brett-Surman Ph.D. Dinosaurs are the most popular animals of all time, and the most misunderstood. Dinosaurs did not fly in the air and did not live in the oceans, nor on lake bottoms. Not all large "prehistoric monsters" are dinosaurs. The most famous NON-dinosaurs are plesiosaurs, moso- saurs, pelycosaurs, pterodactyls and ichthyosaurs. Any name ending in 'saurus' is not automatically a dinosaur, for' example, Mastodonto- saurus is neither a mastodon nor a dinosaur - it is an amphibian! Dinosaurs are defined by a combination of skeletal features that cannot readily be seen when the animal is fully restored in a flesh reconstruction. Because of the confusion, this compilation is offered as a checklist for the collector. This topical list compiles all the dinosaurs on stamps where the actual bones are pictured or whole restorations are used. It excludes footprints (as used in the Lesotho stamps), cartoons (as in the 1984 issue from Gambia), silhouettes (Ascension Island # 305) and unoffi- cial issues such as the famous Sinclair Dinosaur stamps. The name "Brontosaurus", which appears on many stamps, is used with quotation marks to denote it as a popular name in contrast to its correct scientific name, Apatosaurus. For those interested in a detailed encyclopedic work about all fossils on stamps, the reader is referred to the forthcoming book, 'Paleontology - a Guide to the Postal Materials Depicting Prehistoric Lifeforms' by Fran Adams et. al. The best book currently in print is a book titled 'Dinosaur Stamps of the World' by Baldwin & Halstead. -
Titanosaur, Titano- Sauridae
Cambridge University Press 978-0-521-77930-2 - Dinosaur Impressions: Postcards from a Paleontologist Philippe Taquet Index More information INDEX FOR ECONOMY, informal and formal names of taxa (titanosaur, Titano sauridae) as well as eponymous genera (Titanosaurus) are often listed under a single joint entry. Illustration pages are followed by an "f." Bachelet. Abbe. 177 Afrovenator, 220 Agades, 2, 3,4, 5, 15,22,25, 53, 63, 66 Bacot. J., l30-1 Air. 3. 4. 53. 66 Baharija. 19lf., 192 Aix-en-Provence. 169, 198-200 Bahia. 81-2. 83-4. 92-4 Alexander. R. M .. 59 Bakker, R. T.. 118-21, 202, 203 Algui Ulan Tsav, 133, 136. l37 6. 7 barkhanes. Allport. S .• 82. 93 Barsbold. R .. 124. 128. l30. l37. 145 Alvarez. 1.. 208. 216 Baryonychidae. 193 Baryonyx. Alvarez. W., 208 Battuta, I., 4 American Museum of Natural History. Bayeux. 187 125-8. 138. 144, 151. 223 Bayn Dzak, 127. 128. 134. 138 Andrews. R. c.. 125-8. l34. l38. 223 Beaumont. E. de. 215. 217 Ankylosauria, 33. 35, 132. 200, 225 Beni Mellat, 95, 96. 100 Annam, Annamite Range, 147. 149, 160 Bernissart. 30. 33. 38, 41 66 Bertrand. M .. 96-7 anou, Aodelbi.66 Bessonat. G .. 62 Aoulef. 75. 76 Bidou. H .. 117 44-5, 113, 115 biogeography. 89. 220 Apatosaurus. birds, 194-8. 207 Araripesaurus, 92 90-1. 92. 93. 94 relationship to dinosaurs, 195-8. 205. Araripesuchus. 194-7. 224 223 Archaeopteryx. Archibald. J. D., 207 Bleustein-Blanchot. M .. 71 Archosauria. 34. 201-2. 220 Bonaparte. J. F.. 220. 222 Argentina, 220-1 Boulenger. -
The Princeton Field Guide to Dinosaurs, Second Edition
MASS ESTIMATES - DINOSAURS ETC (largely based on models) taxon k model femur length* model volume ml x specific gravity = model mass g specimen (modeled 1st):kilograms:femur(or other long bone length)usually in decameters kg = femur(or other long bone)length(usually in decameters)3 x k k = model volume in ml x specific gravity(usually for whole model) then divided/model femur(or other long bone)length3 (in most models femur in decameters is 0.5253 = 0.145) In sauropods the neck is assigned a distinct specific gravity; in dinosaurs with large feathers their mass is added separately; in dinosaurs with flight ablity the mass of the fight muscles is calculated separately as a range of possiblities SAUROPODS k femur trunk neck tail total neck x 0.6 rest x0.9 & legs & head super titanosaur femur:~55000-60000:~25:00 Argentinosaurus ~4 PVPH-1:~55000:~24.00 Futalognkosaurus ~3.5-4 MUCPv-323:~25000:19.80 (note:downsize correction since 2nd edition) Dreadnoughtus ~3.8 “ ~520 ~75 50 ~645 0.45+.513=.558 MPM-PV 1156:~26000:19.10 Giraffatitan 3.45 .525 480 75 25 580 .045+.455=.500 HMN MB.R.2181:31500(neck 2800):~20.90 “XV2”:~45000:~23.50 Brachiosaurus ~4.15 " ~590 ~75 ~25 ~700 " +.554=~.600 FMNH P25107:~35000:20.30 Europasaurus ~3.2 “ ~465 ~39 ~23 ~527 .023+.440=~.463 composite:~760:~6.20 Camarasaurus 4.0 " 542 51 55 648 .041+.537=.578 CMNH 11393:14200(neck 1000):15.25 AMNH 5761:~23000:18.00 juv 3.5 " 486 40 55 581 .024+.487=.511 CMNH 11338:640:5.67 Chuanjiesaurus ~4.1 “ ~550 ~105 ~38 ~693 .063+.530=.593 Lfch 1001:~10700:13.75 2 M. -
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’’. -
Brains and Intelligence
BRAINS AND INTELLIGENCE The EQ or Encephalization Quotient is a simple way of measuring an animal's intelligence. EQ is the ratio of the brain weight of the animal to the brain weight of a "typical" animal of the same body weight. Assuming that smarter animals have larger brains to body ratios than less intelligent ones, this helps determine the relative intelligence of extinct animals. In general, warm-blooded animals (like mammals) have a higher EQ than cold-blooded ones (like reptiles and fish). Birds and mammals have brains that are about 10 times bigger than those of bony fish, amphibians, and reptiles of the same body size. The Least Intelligent Dinosaurs: The primitive dinosaurs belonging to the group sauropodomorpha (which included Massospondylus, Riojasaurus, and others) were among the least intelligent of the dinosaurs, with an EQ of about 0.05 (Hopson, 1980). Smartest Dinosaurs: The Troodontids (like Troödon) were probably the smartest dinosaurs, followed by the dromaeosaurid dinosaurs (the "raptors," which included Dromeosaurus, Velociraptor, Deinonychus, and others) had the highest EQ among the dinosaurs, about 5.8 (Hopson, 1980). The Encephalization Quotient was developed by the psychologist Harry J. Jerison in the 1970's. J. A. Hopson (a paleontologist from the University of Chicago) did further development of the EQ concept using brain casts of many dinosaurs. Hopson found that theropods (especially Troodontids) had higher EQ's than plant-eating dinosaurs. The lowest EQ's belonged to sauropods, ankylosaurs, and stegosaurids. A SECOND BRAIN? It used to be thought that the large sauropods (like Brachiosaurus and Apatosaurus) and the ornithischian Stegosaurus had a second brain. -
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. -
Note on the Sauropod and Theropod Dinosaurs from the Upper Cretaceous of Madagascar*
EXTRACT FROM THE BULLETIN DE LA SOCIÉTÉ GÉOLOGIQUE DE FRANCE 3rd series, volume XXIV, page 176, 1896. NOTE ON THE SAUROPOD AND THEROPOD DINOSAURS FROM THE UPPER CRETACEOUS OF MADAGASCAR* by Charles DEPÉRET. (PLATE VI). Translated by Matthew Carrano Department of Anatomical Sciences SUNY at Stony Brook, September 1999 The bones of large dinosaurian reptiles described in this work were brought to me by my good friend, Mr. Dr. Félix Salètes, primary physician for the Madagascar expedition, from the environs of Maevarana, where he was charged with installing a provisional hospital. This locality is situated on the right bank of the eastern arm of the Betsiboka, 46 kilometers south of Majunga, on the northwest coast of the island of Madagascar. Not having the time to occupy himself with paleontological studies, Dr. Salètes charged one of his auxiliary agents, Mr. Landillon, company sergeant-major of the marines, with researching the fossils in the environs of the Maevarana post. Thanks to the zeal and activity of Mr. Landillon, who was not afraid to gravely expose his health in these researches, I have been able to receive the precious bones of terrestrial reptiles that are the object of this note, along with an important series of fossil marine shells. I eagerly seize the opportunity here to thank Mr. Landillon for his important shipment and for the very precise geological data which he communicated to me concerning the environs of Maevarana, and of which I will now give a short sketch. 1st. Geology of Maevarana and placement of the localities. * Original reference: Depéret, C. -
Dinosaurs British Isles
DINOSAURS of the BRITISH ISLES Dean R. Lomax & Nobumichi Tamura Foreword by Dr Paul M. Barrett (Natural History Museum, London) Skeletal reconstructions by Scott Hartman, Jaime A. Headden & Gregory S. Paul Life and scene reconstructions by Nobumichi Tamura & James McKay CONTENTS Foreword by Dr Paul M. Barrett.............................................................................10 Foreword by the authors........................................................................................11 Acknowledgements................................................................................................12 Museum and institutional abbreviations...............................................................13 Introduction: An age-old interest..........................................................................16 What is a dinosaur?................................................................................................18 The question of birds and the ‘extinction’ of the dinosaurs..................................25 The age of dinosaurs..............................................................................................30 Taxonomy: The naming of species.......................................................................34 Dinosaur classification...........................................................................................37 Saurischian dinosaurs............................................................................................39 Theropoda............................................................................................................39 -
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. -
Re-Description of the Sauropod Dinosaur Amanzia (“Ornithopsis
Schwarz et al. Swiss J Geosci (2020) 113:2 https://doi.org/10.1186/s00015-020-00355-5 Swiss Journal of Geosciences ORIGINAL PAPER Open Access Re-description of the sauropod dinosaur Amanzia (“Ornithopsis/Cetiosauriscus”) greppini n. gen. and other vertebrate remains from the Kimmeridgian (Late Jurassic) Reuchenette Formation of Moutier, Switzerland Daniela Schwarz1* , Philip D. Mannion2 , Oliver Wings3 and Christian A. Meyer4 Abstract Dinosaur remains were discovered in the 1860’s in the Kimmeridgian (Late Jurassic) Reuchenette Formation of Moutier, northwestern Switzerland. In the 1920’s, these were identifed as a new species of sauropod, Ornithopsis greppini, before being reclassifed as a species of Cetiosauriscus (C. greppini), otherwise known from the type species (C. stewarti) from the late Middle Jurassic (Callovian) of the UK. The syntype of “C. greppini” consists of skeletal elements from all body regions, and at least four individuals of diferent sizes can be distinguished. Here we fully re-describe this material, and re-evaluate its taxonomy and systematic placement. The Moutier locality also yielded a theropod tooth, and fragmen- tary cranial and vertebral remains of a crocodylomorph, also re-described here. “C.” greppini is a small-sized (not more than 10 m long) non-neosauropod eusauropod. Cetiosauriscus stewarti and “C.” greppini difer from each other in: (1) size; (2) the neural spine morphology and diapophyseal laminae of the anterior caudal vertebrae; (3) the length-to-height proportion in the middle caudal vertebrae; (4) the presence or absence of ridges and crests on the middle caudal cen- tra; and (5) the shape and proportions of the coracoid, humerus, and femur. -
Dinosaur Species List E to M
Dinosaur Species List E to M E F G • Echinodon becklesii • Fabrosaurus australis • Gallimimus bullatus • Edmarka rex • Frenguellisaurus • Garudimimus brevipes • Edmontonia longiceps ischigualastensis • Gasosaurus constructus • Edmontonia rugosidens • Fulengia youngi • Gasparinisaura • Edmontosaurus annectens • Fulgurotherium australe cincosaltensis • Edmontosaurus regalis • Genusaurus sisteronis • Edmontosaurus • Genyodectes serus saskatchewanensis • Geranosaurus atavus • Einiosaurus procurvicornis • Gigantosaurus africanus • Elaphrosaurus bambergi • Giganotosaurus carolinii • Elaphrosaurus gautieri • Gigantosaurus dixeyi • Elaphrosaurus iguidiensis • Gigantosaurus megalonyx • Elmisaurus elegans • Gigantosaurus robustus • Elmisaurus rarus • Gigantoscelus • Elopteryx nopcsai molengraaffi • Elosaurus parvus • Gilmoreosaurus • Emausaurus ernsti mongoliensis • Embasaurus minax • Giraffotitan altithorax • Enigmosaurus • Gongbusaurus shiyii mongoliensis • Gongbusaurus • Eoceratops canadensis wucaiwanensis • Eoraptor lunensis • Gorgosaurus lancensis • Epachthosaurus sciuttoi • Gorgosaurus lancinator • Epanterias amplexus • Gorgosaurus libratus • Erectopus sauvagei • "Gorgosaurus" novojilovi • Erectopus superbus • Gorgosaurus sternbergi • Erlikosaurus andrewsi • Goyocephale lattimorei • Eucamerotus foxi • Gravitholus albertae • Eucercosaurus • Gresslyosaurus ingens tanyspondylus • Gresslyosaurus robustus • Eucnemesaurus fortis • Gresslyosaurus torgeri • Euhelopus zdanskyi • Gryponyx africanus • Euoplocephalus tutus • Gryponyx taylori • Euronychodon -
Redalyc.Angolatitan Adamastor, a New Sauropod Dinosaur and the First Record from Angola
Anais da Academia Brasileira de Ciências ISSN: 0001-3765 [email protected] Academia Brasileira de Ciências Brasil MATEUS, OCTÁVIO; JACOBS, LOUIS L.; SCHULP, ANNE S.; POLCYN, MICHAEL J.; TAVARES, TATIANA S.; BUTA NETO, ANDRÉ; MORAIS, MARIA LUÍSA; ANTUNES, MIGUEL T. Angolatitan adamastor, a new sauropod dinosaur and the first record from Angola Anais da Academia Brasileira de Ciências, vol. 83, núm. 1, marzo, 2011, pp. 221-233 Academia Brasileira de Ciências Rio de Janeiro, Brasil Available in: http://www.redalyc.org/articulo.oa?id=32717681011 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative “main” — 2011/2/10 — 15:47 — page 221 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 221-233 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc Angolatitan adamastor, a new sauropod dinosaur and the first record from Angola , OCTÁVIO MATEUS1 2, LOUIS L. JACOBS3, ANNE S. SCHULP4, MICHAEL J. POLCYN3, TATIANA S. TAVARES5, ANDRÉ BUTA NETO5, MARIA LUÍSA MORAIS5 and MIGUEL T. ANTUNES6 1CICEGe, Faculdade de Ciências e Tecnologia, FCT, Universidade Nova de Lisboa, 2829-516 Caparica, Portugal 2Museu da Lourinhã, Rua João Luis de Moura, 2530-157 Lourinhã, Portugal 3Huffington Department of Earth Sciences, Southern Methodist University, Dallas, TX, 75275, USA 4Natuurhistorisch Museum Maastricht, de Bosquetplein 6-7, NL6211 KJ Maastricht, The Netherlands 5Geology Department, Universidade Agostinho Neto, Av.