Objects from Doncaster Museum and Art Gallery's Palaeontology Collection
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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. -
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. -
Geological Survey of Ohio
GEOLOGICAL SURVEY OF OHIO. VOL. I.—PART II. PALÆONTOLOGY. SECTION II. DESCRIPTIONS OF FOSSIL FISHES. BY J. S. NEWBERRY. Digital version copyrighted ©2012 by Don Chesnut. THE CLASSIFICATION AND GEOLOGICAL DISTRIBUTION OF OUR FOSSIL FISHES. So little is generally known in regard to American fossil fishes, that I have thought the notes which I now give upon some of them would be more interesting and intelligible if those into whose hands they will fall could have a more comprehensive view of this branch of palæontology than they afford. I shall therefore preface the descriptions which follow with a few words on the geological distribution of our Palæozoic fishes, and on the relations which they sustain to fossil forms found in other countries, and to living fishes. This seems the more necessary, as no summary of what is known of our fossil fishes has ever been given, and the literature of the subject is so scattered through scientific journals and the proceedings of learned societies, as to be practically inaccessible to most of those who will be readers of this report. I. THE ZOOLOGICAL RELATIONS OF OUR FOSSIL FISHES. To the common observer, the class of Fishes seems to be well defined and quite distin ct from all the other groups o f vertebrate animals; but the comparative anatomist finds in certain unusual and aberrant forms peculiarities of structure which link the Fishes to the Invertebrates below and Amphibians above, in such a way as to render it difficult, if not impossible, to draw the lines sharply between these great groups. -
Steneosaurus Brevior
The mystery of Mystriosaurus: Redescribing the poorly known Early Jurassic teleosauroid thalattosuchians Mystriosaurus laurillardi and Steneosaurus brevior SVEN SACHS, MICHELA M. JOHNSON, MARK T. YOUNG, and PASCAL ABEL Sachs, S., Johnson, M.M., Young, M.T., and Abel, P. 2019. The mystery of Mystriosaurus: Redescribing the poorly known Early Jurassic teleosauroid thalattosuchians Mystriosaurus laurillardi and Steneosaurus brevior. Acta Palaeontologica Polonica 64 (3): 565–579. The genus Mystriosaurus, established by Kaup in 1834, was one of the first thalattosuchian genera to be named. The holotype, an incomplete skull from the lower Toarcian Posidonienschiefer Formation of Altdorf (Bavaria, southern Germany), is poorly known with a convoluted taxonomic history. For the past 60 years, Mystriosaurus has been consid- ered a subjective junior synonym of Steneosaurus. However, our reassessment of the Mystriosaurus laurillardi holotype demonstrates that it is a distinct and valid taxon. Moreover, we find the holotype of “Steneosaurus” brevior, an almost complete skull from the lower Toarcian Whitby Mudstone Formation of Whitby (Yorkshire, UK), to be a subjective ju- nior synonym of M. laurillardi. Mystriosaurus is diagnosed in having: a heavily and extensively ornamented skull; large and numerous neurovascular foramina on the premaxillae, maxillae and dentaries; anteriorly oriented external nares; and four teeth per premaxilla. Our phylogenetic analyses reveal M. laurillardi to be distantly related to Steneosaurus bollensis, supporting our contention that they are different taxa. Interestingly, our analyses hint that Mystriosaurus may be more closely related to the Chinese teleosauroid (previously known as Peipehsuchus) than any European form. Key words: Thalattosuchia, Teleosauroidea, Mystriosaurus, Jurassic, Toarcian Posidonienschiefer Formation, Whitby Mudstone Formation, Germany, UK. -
Occurrence of Torvoneustes (Crocodylomorpha, Metriorhynchidae) in Marine Jurassic Deposits of Oaxaca, Mexico
Rev. bras. paleontol. 19(3):415-424, Setembro/Dezembro 2016 © 2016 by the Sociedade Brasileira de Paleontologia doi: 10.4072/rbp.2016.3.07 OCCURRENCE OF TORVONEUSTES (CROCODYLOMORPHA, METRIORHYNCHIDAE) IN MARINE JURASSIC DEPOSITS OF OAXACA, MEXICO JAIR I. BARRIENTOS-LARA Posgrado en Ciencias Biológicas, Instituto de Geología, Universidad Nacional Autónoma de México, Circuito de la Investigación S/N, Ciudad Universitaria, Delegación Coyoacán, Distrito Federal, 04510, México. [email protected] YANINA HERRERA, MARTA S. FERNÁNDEZ División Paleontología Vertebrados, Unidades de Investigación Anexo Museo, Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, Av. 60 y 122, B1900AVW, La Plata, Argentina. [email protected], [email protected] JESÚS ALVARADO-ORTEGA Instituto de Geología, Universidad Nacional Autónoma de México, Circuito de la Investigación s/n, Ciudad Universitaria, Delegación Coyoacán, Distrito Federal, 04510, México. [email protected] ABSTRACT – IGM 9026 is a singular fossil collected at the beginning of the 20th century in an improperly documented site within the Tlaxiaco Basin, near to Tlaxiaco town, Oaxaca, Mexico. The age of the site was suggested as being early Cretaceous. This specimen is the holotype of Plesiosaurus (Polypticodon) mexicanus, which later was identified as a possible late Jurassic marine crocodylomorph of the family Metriorhynchidae, and consequently it was referred as ?Cricosaurus mexicanus. The present study provides a re-description of this fossil based on a microscopic analysis and the use of white and UV lights; these analyses led to the discovery of peculiar dental characters diagnostic of the genus Torvoneustes. This finding supports the re-classification of IGM 9026 under a new nominal combination asTorvoneustes mexicanus. -
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 -
The First Dinosaur Egg Remains a Mystery
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.10.406678; this version posted December 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 The first dinosaur egg remains a mystery 2 3 Lucas J. Legendre1*, David Rubilar-Rogers2, Alexander O. Vargas3, and Julia A. 4 Clarke1* 5 6 1Department of Geological Sciences, University of Texas at Austin, Austin, Texas 78756, 7 USA. 8 2Área Paleontología, Museo Nacional de Historia Natural, Casilla 787, Santiago, Chile. 9 3Departamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago 7800003, 10 Chile. 11 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.12.10.406678; this version posted December 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 12 Abstract 13 A recent study by Norell et al. (2020) described new egg specimens for two dinosaur species, 14 identified as the first soft-shelled dinosaur eggs. The authors used phylogenetic comparative 15 methods to reconstruct eggshell type in a sample of reptiles, and identified the eggs of 16 dinosaurs and archosaurs as ancestrally soft-shelled, with three independent acquisitions of a 17 hard eggshell among dinosaurs. This result contradicts previous hypotheses of hard-shelled 18 eggs as ancestral to archosaurs and dinosaurs. -
The Geology of Susquehanna County and Wayne County
This is a reproduction of a library book that was digitized by Google as part of an ongoing effort to preserve the information in books and make it universally accessible. https://books.google.com Hi lH -:. I \:^<m. mm mm m ■H ^IVBKS^OFMICHJ^ GLE- SECOND GEOLOGICAL SURVEY OF PENNSYLVANIA: REPORT OF PROGRESS G5. H^ l0Jz THE GEOLOGY Susquehanna county WAYNE COUNTY. By I. C. WHITE. WITH A GEOLOGICALLY COLORED MAP, AND 58 SECTIONS. HARRISBURG: PUBLISHED BY THE BOARD OF COMMISSIONERS TOn THE SECOND GEOLOGICAL SURVEY. 1881. Entered, for the Commonwealth of Pennsylvania, in the year 1880, according to acts of Congress, By WILLIAM A. INGHAM, Secretary of the Board of Commissioners of Geological Survey, In the office of the Librarian of Congress, at Washington, D. C. Electrotyped and printed by LANE S. HART, State Printer, Harrisburg, Pa. BOARD OF COMMISSIONERS. His Excellency, HENRY M. HOYT, Governor, and ex-officio President of the Board, Harrisburg. Ario Pardee, ---------- Hazleton. William A. Ingham, ------- Philadelphia. Henry S. Eckert, -------- Reading. Henry McCormick, - - - Harrisburg. James Macfarlane, -------- Towanda. Charles A. Miner, - - ----- - Luzerne co. Joseph Willcox, -------- Philadelphia. Hon. Daniel J. Morrell, ------ Johnstown. Louis W. Hall, - - - - ----- Harrisburg. Samuel Q. Brown, - - - ----- Pleasantville. SECRETARY OF THE BOARD. William A. Ingham, ------- Philadelphia. STATE GEOLOGIST. Peter Lesley, ---------- Philadelphia. ASSISTANTS IN 1881. John F. Carll, geologist for the Oil regions ; address Pleasantville, Venango county, Pa. J. Sutton Wall, to report on the coal and collieries of the Monongahela re gion ; address Monongahela city, Pa. J. J. Stevenson, geologist for Bedford and Fulton counties ; address Union- town, Fayette county, Pa. W. G. Platt, geologist for Centre and Clearfield counties ; address 907 Wal nut street, Philadelphia. -
Short Review of the Present Knowledge of the Sauropoda
PRESENT KNOWLEDGE OF THE SAUROl'ODA.-HUENE. 121 SHORT REVIEW OF THE PRESENT KNOWLEDGE OF THE SAUROPODA. BY DR. FRIEDRICH BARON HUENE, PROFESSOR AT THE UNIVERSITY OF TUBINGEN, GERMANY. THE Sauropoda are the hugest continental animals the earth has ever seen. They lived from the middle Jurassic to the Danian period of the upper most Cretaceous. Much has been written about them, but nevertheless their natura! classification and development do not yet appear in a desirable clearness. In this respect the immense size of the Sauropoda has been an obstacle. The satisfactory excavation of such gigant.ic skeletons is difficult, and the preparation, which is still more important, needs trained, skilful men working for years. The scientific value of a skeleton is determined in advance by the degree of care by which, during the excavation, the original articulation or the original positions of the bones to each other in the rock is dealt "\vith by sketch-plans in scale as to make sure specially the sequence of the vertebræ. Because of the failure of this in many cases, we still know so astonishingly little about the natura! classification of the Sauropoda as a whole. Most has been written and spoken on the North American Sauropoda. Too little has been done with the earlier Sauropoda. The knowledge of the Upper Cretaceous Sauropoda until now is quite insufficient. The large amount of Tendaguru Sauropoda at Berlin and the recent excavations of the Carnegie Museum at Pittsburgh have not yet been described ; they will probably complete and alter our ideas of the development and classification of the Sauropoda. -
I Ecomorphological Change in Lobe-Finned Fishes (Sarcopterygii
Ecomorphological change in lobe-finned fishes (Sarcopterygii): disparity and rates by Bryan H. Juarez A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science (Ecology and Evolutionary Biology) in the University of Michigan 2015 Master’s Thesis Committee: Assistant Professor Lauren C. Sallan, University of Pennsylvania, Co-Chair Assistant Professor Daniel L. Rabosky, Co-Chair Associate Research Scientist Miriam L. Zelditch i © Bryan H. Juarez 2015 ii ACKNOWLEDGEMENTS I would like to thank the Rabosky Lab, David W. Bapst, Graeme T. Lloyd and Zerina Johanson for helpful discussions on methodology, Lauren C. Sallan, Miriam L. Zelditch and Daniel L. Rabosky for their dedicated guidance on this study and the London Natural History Museum for courteously providing me with access to specimens. iii TABLE OF CONTENTS ACKNOWLEDGEMENTS ii LIST OF FIGURES iv LIST OF APPENDICES v ABSTRACT vi SECTION I. Introduction 1 II. Methods 4 III. Results 9 IV. Discussion 16 V. Conclusion 20 VI. Future Directions 21 APPENDICES 23 REFERENCES 62 iv LIST OF TABLES AND FIGURES TABLE/FIGURE II. Cranial PC-reduced data 6 II. Post-cranial PC-reduced data 6 III. PC1 and PC2 Cranial and Post-cranial Morphospaces 11-12 III. Cranial Disparity Through Time 13 III. Post-cranial Disparity Through Time 14 III. Cranial/Post-cranial Disparity Through Time 15 v LIST OF APPENDICES APPENDIX A. Aquatic and Semi-aquatic Lobe-fins 24 B. Species Used In Analysis 34 C. Cranial and Post-Cranial Landmarks 37 D. PC3 and PC4 Cranial and Post-cranial Morphospaces 38 E. PC1 PC2 Cranial Morphospaces 39 1-2. -
Big-Headed Marine Crocodyliforms and Why We Must Be Cautious When Using Extant Species As Body Length Proxies for Long-Extinct Relatives
Palaeontologia Electronica palaeo-electronica.org Big-headed marine crocodyliforms and why we must be cautious when using extant species as body length proxies for long-extinct relatives Mark T. Young, Márton Rabi, Mark A. Bell, Davide Foffa, Lorna Steel, Sven Sachs, and Karin Peyer ABSTRACT Body size is commonly used as a key variable for estimating ecomorphological trends at a macroevolutionary scale, making reliable body length estimates of fossil taxa critically important. Crocodylomorphs (extant crocodylians and their extinct rela- tives) evolved numerous 'aberrant' body-plans during their ~230 million-year history, ranging from ‘hooved’ terrestrial species to dolphin-like pelagic species. Such clades evolved distinct cranial and femoral scaling ratios (compared to total body length), thereby making extant taxa unsuitable proxies for estimating their body lengths. Here we illustrate that the fossil clade Teleosauridae also fits into this category. Teleosaurids were a predominately shallow marine clade that had a global distribution during the Jurassic. Known to have evolved a wide range of body lengths (2–5 m based on com- plete skeletons), there is currently no way of reliably estimating the size of incomplete specimens. This is surprising, as some teleosaurids have been considered very large (9–10 m in total length), thus making Teleosauridae the largest bodied clade during the first 100 million years of crocodylomorph evolution. Our examination and regression analyses of the best preserved teleosaurid skeletons demonstrates that: they were smaller than previously thought, with no known specimen exceeding 7.2 m in length; and that they had proportionally large skulls, and proportionally short femora, when compared to body length. -
Fossils Provide Better Estimates of Ancestral Body Size Than Do Extant
Acta Zoologica (Stockholm) 90 (Suppl. 1): 357–384 (January 2009) doi: 10.1111/j.1463-6395.2008.00364.x FossilsBlackwell Publishing Ltd provide better estimates of ancestral body size than do extant taxa in fishes James S. Albert,1 Derek M. Johnson1 and Jason H. Knouft2 Abstract 1Department of Biology, University of Albert, J.S., Johnson, D.M. and Knouft, J.H. 2009. Fossils provide better Louisiana at Lafayette, Lafayette, LA estimates of ancestral body size than do extant taxa in fishes. — Acta Zoologica 2 70504-2451, USA; Department of (Stockholm) 90 (Suppl. 1): 357–384 Biology, Saint Louis University, St. Louis, MO, USA The use of fossils in studies of character evolution is an active area of research. Characters from fossils have been viewed as less informative or more subjective Keywords: than comparable information from extant taxa. However, fossils are often the continuous trait evolution, character state only known representatives of many higher taxa, including some of the earliest optimization, morphological diversification, forms, and have been important in determining character polarity and filling vertebrate taphonomy morphological gaps. Here we evaluate the influence of fossils on the interpretation of character evolution by comparing estimates of ancestral body Accepted for publication: 22 July 2008 size in fishes (non-tetrapod craniates) from two large and previously unpublished datasets; a palaeontological dataset representing all principal clades from throughout the Phanerozoic, and a macroecological dataset for all 515 families of living (Recent) fishes. Ancestral size was estimated from phylogenetically based (i.e. parsimony) optimization methods. Ancestral size estimates obtained from analysis of extant fish families are five to eight times larger than estimates using fossil members of the same higher taxa.