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A Comprehensive Anatomical And
Journal of Paleontology, Volume 94, Memoir 78, 2020, p. 1–103 Copyright © 2020, The Paleontological Society. This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/ licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. 0022-3360/20/1937-2337 doi: 10.1017/jpa.2020.14 A comprehensive anatomical and phylogenetic evaluation of Dilophosaurus wetherilli (Dinosauria, Theropoda) with descriptions of new specimens from the Kayenta Formation of northern Arizona Adam D. Marsh1,2 and Timothy B. Rowe1 1Jackson School of Geosciences, the University of Texas at Austin, 2305 Speedway Stop C1160, Austin, Texas 78712, USA <[email protected]><[email protected]> 2Division of Resource Management, Petrified Forest National Park, 1 Park Road #2217, Petrified Forest, Arizona 86028, USA Abstract.—Dilophosaurus wetherilli was the largest animal known to have lived on land in North America during the Early Jurassic. Despite its charismatic presence in pop culture and dinosaurian phylogenetic analyses, major aspects of the skeletal anatomy, taxonomy, ontogeny, and evolutionary relationships of this dinosaur remain unknown. Skeletons of this species were collected from the middle and lower part of the Kayenta Formation in the Navajo Nation in northern Arizona. Redescription of the holotype, referred, and previously undescribed specimens of Dilophosaurus wetherilli supports the existence of a single species of crested, large-bodied theropod in the Kayenta Formation. The parasagittal nasolacrimal crests are uniquely constructed by a small ridge on the nasal process of the premaxilla, dorsoventrally expanded nasal, and tall lacrimal that includes a posterior process behind the eye. -
R~;: PHYSIOLOGICAL, MIGRATORIAL
....----------- 'r~;: i ! 'r; Pa/eont .. 62(4), 1988, pp. 64~52 Copyright © 1988, The Paleontological Society 0022-3360/88/0062-0640$03.00 PHYSIOLOGICAL, MIGRATORIAL, CLIMATOLOGICAL, GEOPHYSICAL, SURVIVAL, AND EVOLUTIONARY IMPLICATIONS OF CRETACEOUS POLAR DINOSAURS GREGORY S. PAUL 3109 North Calvert Street, Baltimore, Maryland 21218 ABSTRACTT- he presence of Late Cretaceous social dinosaurs in polar regions confronted them with winter conditions of extended dark, coolness, breezes, and precipitation that could best be coped with via an endothermic homeothermic physiology of at least the tenrec level. This is true whether the dinosaurs stayed year round in the polar regime-which in North America extended from Alaska south to Montana-or if they migrated away from polar winters. More reptilian physiologies fail to meet the demands of such winters -in certain key ways, a· point tentatively confirmed by the apparent failure of giant Late Cretaceous phobosuchid crocodilians to dwell north of Montana. Low metabolisms were also insufficient for extended annual migrations away from and towards the poles. It is shown that even high metabolic rate dinosaurs probably remained in their polar habitats year-round. The possibility that dinosaurs had avian-mammalian metabolic systems, and may have borne insulation at least seasonally, severely limits their use as polar paleoclimatic and Earth axial tilt indicators. Polar dinosaurs may have been a center of dinosaur evolution. The possible ability of polar dinosaurs to cope with conditions of cool and dark challenges theories that a gradual temperature decline, or a sudden, meteoritic or volcanic induced collapse in temperature and sunlight, destroyed the dinosaurs. INTRODUCTION America suggests that dinosaurs were regularly crossing, and NCREASINGNUMBERSof remains show that dinosaurs lived living upon, the Bering Land Bridge within a few degrees of the I near the North and South Poles during the Cretaceous. -
State of the Palaeoart
Palaeontologia Electronica http://palaeo-electronica.org State of the Palaeoart Mark P. Witton, Darren Naish, and John Conway The discipline of palaeoart, a branch of natural history art dedicated to the recon- struction of extinct life, is an established and important component of palaeontological science and outreach. For more than 200 years, palaeoartistry has worked closely with palaeontological science and has always been integral to the enduring popularity of prehistoric animals with the public. Indeed, the perceived value or success of such products as popular books, movies, documentaries, and museum installations can often be linked to the quality and panache of its palaeoart more than anything else. For all its significance, the palaeoart industry ment part of this dialogue in the published is often poorly treated by the academic, media and literature, in turn bringing the issues concerned to educational industries associated with it. Many wider attention. We argue that palaeoartistry is standard practises associated with palaeoart pro- both scientifically and culturally significant, and that duction are ethically and legally problematic, stifle improved working practises are required by those its scientific and cultural growth, and have a nega- involved in its production. We hope that our views tive impact on the financial viability of its creators. inspire discussion and changes sorely needed to These issues create a climate that obscures the improve the economy, quality and reputation of the many positive contributions made by palaeoartists palaeoart industry and its contributors. to science and education, while promoting and The historic, scientific and economic funding derivative, inaccurate, and sometimes exe- significance of palaeoart crable artwork. -
A Bird's Eye View of the Evolution of Avialan Flight
Chapter 12 Navigating Functional Landscapes: A Bird’s Eye View of the Evolution of Avialan Flight HANS C.E. LARSSON,1 T. ALEXANDER DECECCHI,2 MICHAEL B. HABIB3 ABSTRACT One of the major challenges in attempting to parse the ecological setting for the origin of flight in Pennaraptora is determining the minimal fluid and solid biomechanical limits of gliding and powered flight present in extant forms and how these minima can be inferred from the fossil record. This is most evident when we consider the fact that the flight apparatus in extant birds is a highly integrated system with redundancies and safety factors to permit robust performance even if one or more components of their flight system are outside their optimal range. These subsystem outliers may be due to other adaptive roles, ontogenetic trajectories, or injuries that are accommodated by a robust flight system. This means that many metrics commonly used to evaluate flight ability in extant birds are likely not going to be precise in delineating flight style, ability, and usage when applied to transitional taxa. Here we build upon existing work to create a functional landscape for flight behavior based on extant observations. The functional landscape is like an evolutionary adap- tive landscape in predicting where estimated biomechanically relevant values produce functional repertoires on the landscape. The landscape provides a quantitative evaluation of biomechanical optima, thus facilitating the testing of hypotheses for the origins of complex biomechanical func- tions. Here we develop this model to explore the functional capabilities of the earliest known avialans and their sister taxa. -
Visions of the Prehistoric Past Reviewed by Mark P. Witton
Palaeontologia Electronica http://palaeo-electronica.org Paleoart: Visions of the Prehistoric Past Reviewed by Mark P. Witton Paleoart: Visions of the Prehistoric Past. 2017. Written by Zoë Lescaze and Walton Ford. Taschen. 292 pages, ISBN 978-3-8365-5511-1 (English edition). € 75, £75, $100 (hardcover) Paleoart: Visions of the Prehistoric Past is a collection of palaeoartworks spanning 150 years of palaeoart history, from 1830 to the second half of the 20th century. This huge, supremely well-pre- sented book was primarily written by journalist, archaeological illustrator and art scholar Zoë Les- caze, with an introduction by artist Walton Ford (both are American, and use ‘paleoart’ over the European spelling ‘palaeoart’). Ford states that the genesis of the book reflects “the need for a paleo- art book that was more about the art and less about the paleo” (p. 12), and thus Paleoart skews towards artistic aspects of palaeoartistry rather than palaeontological theory or technical aspects of reconstructing extinct animal appearance. Ford and Lescaze are correct that this angle of palaeo- artistry remains neglected, and this puts Paleoart in prime position to make a big impact on this pop- ular, though undeniably niche subject. Paleoart is extremely well-produced and stun- ning to look at, a visual feast for anyone with an interest in classic palaeoart. 292 pages of thick, sturdy paper (9 chapters, hundreds of images, and four fold outs) and almost impractical dimensions (28 x 37.4 cm) make it a physically imposing, stately tome that reminds us why books belong on shelves and not digital devices. Focusing exclu- sively on 2D art, the layout is minimalist and clean, detail, unobscured by text and labelling. -
Screaming Biplane Dromaeosaurs of the Air. June/July
5c.r~i~ ~l'tp.,ne pr~tl\USp.,urs 1tke.A-ir Written & illustrated by Gregory s. Paul It is questionable whether anyone even speculated that some dinosaurs were feathered until Ostrom detailed the evidence that birds descended from predatory avepod theropods a third of a century ago. The first illustration of a feathered dinosaur was a nice little study of a well ensconced Syntarsus dashing down a dune slope in pursuit of a gliding lizard in Robert Bakker's classic "Dinosaur Renaissance" article in the April 1975 Scientific American by Sarah Landry (can also be seen in the Scientific American Book of the Dinosaur I edited). My first feathered dinosaur was executed shortly after, an inappropriately shaggy Allosaurus attacking a herd of Diplodocus. I was soon doing a host of small theropods in feathers. Despite the logic of feath- / er insulation on the group ancestral birds and showing evidence of a high level energetics, images of feathered avepods were often harshly and unsci- Above: Proposed relationships based on flight adaptations of entifically criticized as unscientific in view of the lack of evidence for their preserved skeletons and feathers of Archaeopteryx, a generalized presence, ignoring the equal fact that no one had found scales on the little Sinornithosaurus, and Confuciusornis, with arrows indicating dinosaurs either. derived adaptations not present in Archaeopteryx as described in In the 1980s I further proposed that the most bird-like, avepectoran text. Not to scale. dinosaurs - dromaeosaurs, troodonts, oviraptorosaurs, and later ther- izinosaurs _were not just close to birds and the origin of flight, but were see- appear to represent the remnants of wings converted to display devices. -
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 -
Alan Feduccia's Riddle of the Feathered Dragons: What Reptiles
Leigh Evolution: Education and Outreach 2014, 7:9 http://www.evolution-outreach.com/content/7/1/9 BOOK REVIEW Open Access Alan Feduccia’s Riddle of the Feathered Dragons: what reptiles gave rise to birds? Egbert Giles Leigh Jr Riddle of the Feathered Dragons: Hidden Birds of China, properly. This is a great pity, for his story is wonderful: by Alan Feduccia. New Haven, CT: Yale University Press, his birds would have made a far better focus for this 2012. Pp. x + 358. H/b $55.00 book than the dispute. This book’s author is at home in the paleontology, So, what is this dispute that spoiled the book? The anatomy, physiology, and behavior of birds. Who could scientific argument is easily summarized. It started be more qualified to write on their origin and evolution? when a paleontologist from Yale University, John Ostrom, This book is unusually, indeed wonderfully, well and unearthed a 75-kg bipedal theropod dinosaur, Deinonychus, clearly illustrated: its producers cannot be praised too buried 110 million years ago in Montana. Deinonychus highly. It is well worth the while of anyone interested in stood a meter tall, and its tail was 1.5 m long. It was active: bird evolution to read it. Although it offers no answers Ostrom thought that both it and Archaeopteryx,which to ‘where birds came from’, it has God’s plenty of fascin- lived 40 million years earlier, were warm-blooded. Deinony- ating, revealing detail, knit together in powerful criticism chus bore many skeletal resemblances to Archaeopteryx, of prevailing views of bird evolution. -
Back Matter (PDF)
Index Note: Page numbers in italic denote figures. Page numbers in bold denote tables. Abel, Othenio (1875–1946) Ashmolean Museum, Oxford, Robert Plot 7 arboreal theory 244 Astrodon 363, 365 Geschichte und Methode der Rekonstruktion... Atlantosaurus 365, 366 (1925) 328–329, 330 Augusta, Josef (1903–1968) 222–223, 331 Action comic 343 Aulocetus sammarinensis 80 Actualism, work of Capellini 82, 87 Azara, Don Felix de (1746–1821) 34, 40–41 Aepisaurus 363 Azhdarchidae 318, 319 Agassiz, Louis (1807–1873) 80, 81 Azhdarcho 319 Agustinia 380 Alexander, Annie Montague (1867–1950) 142–143, 143, Bakker, Robert. T. 145, 146 ‘dinosaur renaissance’ 375–376, 377 Alf, Karen (1954–2000), illustrator 139–140 Dinosaurian monophyly 93, 246 Algoasaurus 365 influence on graphic art 335, 343, 350 Allosaurus, digits 267, 271, 273 Bara Simla, dinosaur discoveries 164, 166–169 Allosaurus fragilis 85 Baryonyx walkeri Altispinax, pneumaticity 230–231 relation to Spinosaurus 175, 177–178, 178, 181, 183 Alum Shale Member, Parapsicephalus purdoni 195 work of Charig 94, 95, 102, 103 Amargasaurus 380 Beasley, Henry Charles (1836–1919) Amphicoelias 365, 366, 368, 370 Chirotherium 214–215, 219 amphisbaenians, work of Charig 95 environment 219–220 anatomy, comparative 23 Beaux, E. Cecilia (1855–1942), illustrator 138, 139, 146 Andrews, Roy Chapman (1884–1960) 69, 122 Becklespinax altispinax, pneumaticity 230–231, Andrews, Yvette 122 232, 363 Anning, Joseph (1796–1849) 14 belemnites, Oxford Clay Formation, Peterborough Anning, Mary (1799–1847) 24, 25, 113–116, 114, brick pits 53 145, 146, 147, 288 Benett, Etheldred (1776–1845) 117, 146 Dimorphodon macronyx 14, 115, 294 Bhattacharji, Durgansankar 166 Hawker’s ‘Crocodile’ 14 Birch, Lt. -
SUPPLEMENTARY INFORMATION Doi:10.1038/Nature24011
SUPPLEMENTARY INFORMATION doi:10.1038/nature24011 1. Details of the new phylogenetic analysis 1.1. Modifications to Baron et al. (2017) data matrix The following list presents all character scoring modifications to the original taxon-character matrix of Baron et al. (2017). Unless explicitly mentioned, specimen numbers without asterisks have been scored from notes and photographs after their first-hand examination by at least one of the authors, specimens marked with † were coded based only on photographic material, and specimens marked with * were coded on direct observation of the specimens. Aardonyx celestae; score modifications based on the first-hand observation of all specimens mentioned in Yates et al. (2010). 19: 0 >1. 21 0 >1. 54: 0 >?. 57: 0 >?. 156: 1 >0. 202: 1 >0. 204: 1 >0. 266: 1 >0. 280: ? >0. Ch 286: 2 >1. 348: 0 >?. 365: ? >1. 376: ? >0. 382: 0 >?. 439: 0 >1. 450: 1 >0. Abrictosaurus consors; score modifications based on NHMUK RU B54†. Further bibliographic source: Sereno (2012). 7: 0>?; 26 0>?; 35. 2>0/1; 47: 0>?; 54 1>?; 369 0>?; 424 1>?. Agilisaurus louderbacki; score modifications based on Barrett et al. (2005) and scorings in Butler et al. (2008) and Barrett et al. (2016). 6: 0>?; 11: 0>1; 35: 1>0; 54: 1>0; 189: ?>0. Agnosphitys cromhallensis; score modifications based on cast of VMNH 1751. Further bibliographic source: Fraser et al. (2001). 15: ? >0; 16: ? >0; 21: ? >1; 24: ? >1; 30: 0 >?; 159: 0 >1; 160: - >0; 164: - >?; 165: ? >0; 167: ? >0; 172: 0 >?; 176: 0 >?; 177: 1 >0; 180: ? >0; 185: 0 >?; 221: 0 >?; 222: 0 >?; 252: 0 >1; 253: 0 >1; 254: 1 >?; 256: 0 >1; 258: 1 >?; 259: ? >0; 292: ? >1; 298: ? >0; 303: 1 >2; 305: 2 >1; 306: ? >2; 315: 1 >0; 317: ? >1; 318: ? >0; 409: ? >0; 411: 1 >0; 419: 1 >0; 421: ? >0. -
ABSTRACT Resurrecting Tyrannosaurus Rex Lauren E. Ammerman Director: Jennifer Good, Ph.D. After the First Successful Extraction
ABSTRACT Resurrecting Tyrannosaurus rex Lauren E. Ammerman Director: Jennifer Good, Ph.D. After the first successful extraction of ancient DNA from a fossilized Quagga in 1984, the subsequent development of PCR (Polymerase Chain Reaction) technology opened up a plethora of possibilities in the field of molecular paleontology. Supplied with fragmented ancient genomes, some scientists acted as if the days of resurrecting dinosaurs were a few technical difficulties away. Theories surfaced on the possible applications of ancient DNA technology, and some, such as creating tactical dinosaurs for the U.S. military, were outrageous. A less ridiculous idea surfaced in the form of Michael Crichton’s Jurassic Park, published in 1990. Coupled with Steven Spielberg’s 1993 feature film adaption, the Jurassic Park series created a world in which genetically- engineered dinosaurs roamed once again as theme park attractions on a billionaire’s private island, and explored the possible outcomes of a “Jurassic Park” experiment. Jurassic Park ignited scientific debate over the technological feasibility, environmental impact, and ethical questions of a “Jurassic Park” experiment. This thesis continues that conversation by asking, could resurrecting a dinosaur be a productive environmental enterprise, other than a mere display of power over Nature? Focusing on Tyrannosaurus rex, this thesis combines a brief survey the current state of dinosaur genetic research, with analyses of rewilding with large predators, to discuss whether or not scientists should ever attempt to re-create a T. rex in the future. APPROVED BY DIRECTOR OF HONORS THESIS Dr. Jennifer Good, Director of University Scholars APPROVED BY THE HONORS PROGRAM Dr. Elizabeth Corey, Director DATE: RESURRECTING TYRANNOSAURUS REX A Thesis Submitted to the Faculty of Baylor University In Partial Fulfillment of the Requirements for the Honors Program By Lauren E. -
Body-Size Evolution in the Dinosauria
8 Body-Size Evolution in the Dinosauria Matthew T. Carrano Introduction The evolution of body size and its influence on organismal biology have received scientific attention since the earliest decades of evolutionary study (e.g., Cope, 1887, 1896; Thompson, 1917). Both paleontologists and neontologists have attempted to determine correlations between body size and numerous aspects of life history, with the ultimate goal of docu- menting both the predictive and causal connections involved (LaBarbera, 1986, 1989). These studies have generated an appreciation for the thor- oughgoing interrelationships between body size and nearly every sig- nificant facet of organismal biology, including metabolism (Lindstedt & Calder, 1981; Schmidt-Nielsen, 1984; McNab, 1989), population ecology (Damuth, 1981; Juanes, 1986; Gittleman & Purvis, 1998), locomotion (Mc- Mahon, 1975; Biewener, 1989; Alexander, 1996), and reproduction (Alex- ander, 1996). An enduring focus of these studies has been Cope’s Rule, the notion that body size tends to increase over time within lineages (Kurtén, 1953; Stanley, 1973; Polly, 1998). Such an observation has been made regarding many different clades but has been examined specifically in only a few (MacFadden, 1986; Arnold et al., 1995; Jablonski, 1996, 1997; Trammer & Kaim, 1997, 1999; Alroy, 1998). The discordant results of such analyses have underscored two points: (1) Cope’s Rule does not apply universally to all groups; and (2) even when present, size increases in different clades may reflect very different underlying processes. Thus, the question, “does Cope’s Rule exist?” is better parsed into two questions: “to which groups does Cope’s Rule apply?” and “what process is responsible for it in each?” Several recent works (McShea, 1994, 2000; Jablonski, 1997; Alroy, 1998, 2000a, 2000b) have begun to address these more specific questions, attempting to quantify patterns of body-size evolution in a phylogenetic (rather than strictly temporal) context, as well as developing methods for interpreting the resultant patterns.