Postcranial Skeletal Pneumaticity in Sauropods and Its
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Novel Form of Postcranial Skeletal Pneumaticity in a Sauropod Dinosaur: Implications for the Paleobiology of Rebbachisauridae
Editors' choice A novel form of postcranial skeletal pneumaticity in a sauropod dinosaur: Implications for the paleobiology of Rebbachisauridae LUCIO M. IBIRICU, MATTHEW C. LAMANNA, RUBÉ N D.F. MARTÍ NEZ, GABRIEL A. CASAL, IGNACIO A. CERDA, GASTÓ N MARTÍ NEZ, and LEONARDO SALGADO Ibiricu, L.M., Lamanna, M.C., Martí nez, R.D.F., Casal, G.A., Cerda, I.A., Martí nez, G., and Salgado, L. 2017. A novel form of postcranial skeletal pneumaticity in a sauropod dinosaur: Implications for the paleobiology of Rebbachisauridae. Acta Palaeontologica Polonica 62 (2): 221–236. In dinosaurs and other archosaurs, the presence of foramina connected with internal chambers in axial and appendic- ular bones is regarded as a robust indicator of postcranial skeletal pneumaticity (PSP). Here we analyze PSP and its paleobiological implications in rebbachisaurid diplodocoid sauropod dinosaurs based primarily on the dorsal verte- brae of Katepensaurus goicoecheai, a rebbachisaurid from the Cenomanian–Turonian (Upper Cretaceous) Bajo Barreal Formation of Patagonia, Argentina. We document a complex of interconnected pneumatic foramina and internal chambers within the dorsal vertebral transverse processes of Katepensaurus. Collectively, these structures constitute a form of PSP that has not previously been observed in sauropods, though it is closely comparable to morphologies seen in selected birds and non-avian theropods. Parts of the skeletons of Katepensaurus and other rebbachisaurid taxa such as Amazonsaurus maranhensis and Tataouinea hannibalis exhibit an elevated degree of pneumaticity relative to the conditions in many other sauropods. We interpret this extensive PSP as an adaptation for lowering the density of the skeleton, and tentatively propose that this reduced skeletal density may also have decreased the muscle energy required to move the body and the heat generated in so doing. -
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’’. -
Ostrich Production Systems Part I: a Review
11111111111,- 1SSN 0254-6019 Ostrich production systems Food and Agriculture Organization of 111160mmi the United Natiorp str. ro ucti s ct1rns Part A review by Dr M.M. ,,hanawany International Consultant Part II Case studies by Dr John Dingle FAO Visiting Scientist Food and , Agriculture Organization of the ' United , Nations Ot,i1 The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. M-21 ISBN 92-5-104300-0 Reproduction of this publication for educational or other non-commercial purposes is authorized without any prior written permission from the copyright holders provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without written permission of the copyright holders. Applications for such permission, with a statement of the purpose and extent of the reproduction, should be addressed to the Director, Information Division, Food and Agriculture Organization of the United Nations, Viale dells Terme di Caracalla, 00100 Rome, Italy. C) FAO 1999 Contents PART I - PRODUCTION SYSTEMS INTRODUCTION Chapter 1 ORIGIN AND EVOLUTION OF THE OSTRICH 5 Classification of the ostrich in the animal kingdom 5 Geographical distribution of ratites 8 Ostrich subspecies 10 The North -
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. -
Estimating Mass Properties of Dinosaurs Using Laser Imaging and 3D Computer Modelling
Estimating Mass Properties of Dinosaurs Using Laser Imaging and 3D Computer Modelling Karl T. Bates1*, Phillip L. Manning2,3, David Hodgetts3, William I. Sellers1 1 Adaptive Organismal Biology Research Group, Faculty of Life Sciences, University of Manchester, Jackson’s Mill, Manchester, United Kingdom, 2 The Manchester Museum, University of Manchester, Manchester, United Kingdom, 3 School of Earth, Atmospheric and Environmental Science, University of Manchester, Manchester, United Kingdom Abstract Body mass reconstructions of extinct vertebrates are most robust when complete to near-complete skeletons allow the reconstruction of either physical or digital models. Digital models are most efficient in terms of time and cost, and provide the facility to infinitely modify model properties non-destructively, such that sensitivity analyses can be conducted to quantify the effect of the many unknown parameters involved in reconstructions of extinct animals. In this study we use laser scanning (LiDAR) and computer modelling methods to create a range of 3D mass models of five specimens of non- avian dinosaur; two near-complete specimens of Tyrannosaurus rex, the most complete specimens of Acrocanthosaurus atokensis and Strutiomimum sedens, and a near-complete skeleton of a sub-adult Edmontosaurus annectens. LiDAR scanning allows a full mounted skeleton to be imaged resulting in a detailed 3D model in which each bone retains its spatial position and articulation. This provides a high resolution skeletal framework around which the body cavity and internal organs such as lungs and air sacs can be reconstructed. This has allowed calculation of body segment masses, centres of mass and moments or inertia for each animal. However, any soft tissue reconstruction of an extinct taxon inevitably represents a best estimate model with an unknown level of accuracy. -
Titanosauriform Teeth from the Cretaceous of Japan
“main” — 2011/2/10 — 15:59 — page 247 — #1 Anais da Academia Brasileira de Ciências (2011) 83(1): 247-265 (Annals of the Brazilian Academy of Sciences) Printed version ISSN 0001-3765 / Online version ISSN 1678-2690 www.scielo.br/aabc Titanosauriform teeth from the Cretaceous of Japan HARUO SAEGUSA1 and YUKIMITSU TOMIDA2 1Museum of Nature and Human Activities, Hyogo, Yayoigaoka 6, Sanda, 669-1546, Japan 2National Museum of Nature and Science, 3-23-1 Hyakunin-cho, Shinjuku-ku, Tokyo 169-0073, Japan Manuscript received on October 25, 2010; accepted for publication on January 7, 2011 ABSTRACT Sauropod teeth from six localities in Japan were reexamined. Basal titanosauriforms were present in Japan during the Early Cretaceous before Aptian, and there is the possibility that the Brachiosauridae may have been included. Basal titanosauriforms with peg-like teeth were present during the “mid” Cretaceous, while the Titanosauria with peg-like teeth was present during the middle of Late Cretaceous. Recent excavations of Cretaceous sauropods in Asia showed that multiple lineages of sauropods lived throughout the Cretaceous in Asia. Japanese fossil records of sauropods are conformable with this hypothesis. Key words: Sauropod, Titanosauriforms, tooth, Cretaceous, Japan. INTRODUCTION humerus from the Upper Cretaceous Miyako Group at Moshi, Iwaizumi Town, Iwate Pref. (Hasegawa et al. Although more than twenty four dinosaur fossil local- 1991), all other localities provided fossil teeth (Tomida ities have been known in Japan (Azuma and Tomida et al. 2001, Tomida and Tsumura 2006, Saegusa et al. 1998, Kobayashi et al. 2006, Saegusa et al. 2008, Ohara 2008, Azuma and Shibata 2010). -
Boletim Informativo Da SBP Ano 35, N° 73, 2020 · ISSN 1807-2550 PALEO 2019
Boletim Informativo da SBP Ano 35, n° 73, 2020 · ISSN 1807-2550 PALEO 2019 RELATOS E RESUMOS SOCIEDADE BRASILEIRA DE PALEONTOLOGIA Presidente: Dr. Renato Pirani Ghilardi (UNESP/Bauru) Vice-Presidente: Dr. Rodrigo Miloni Santucci (UnB) 1ª Secretária: Dra. SoniaMaria Oliveira Agostinho da Silva (UFPE) 2º Secretário: Me. Victor Rodrigues Ribeiro (UNESP/Bauru) 1º Tesoureiro: Me. Marcos César Bissaro Júnior (USP/Ribeirão Preto) 2º Tesoureiro: Dr. Hermínio Ismael de Araújo Junior (UERJ) Diretor de Publicações: Dr. Sandro Marcelo Scheffler (UFRJ) P a l e o n t o l o g i a e m D e s t a q u e Boletim Informativo da Sociedade Brasileira de Paleontologia Ano 35, n° 73, dezembro/2020 · ISSN 1807-2550 Web: http://www.sbpbrasil.org/, Editores: Sandro Marcelo Scheffler, Maria Izabel Lima de Manes. Agradecimentos: Aos organizadores dos eventos científicos. Capa: Afloramento com pegadas de terópodas nas margens do rio Nioaque, Mato Grosso do Sul, durante trabalho de campo. Foto: Rafael Costa da Silva. 1. Paleontologia 2. Paleobiologia 3. Geociências Distribuído sob a Licença de Atribuição Creative Commons. EDITORIAL As Paleos acontecem anualmente e são encontros promovidos pela Sociedade Brasileira de Paleontologia com o objetivo de integrar estudantes, pesquisadores, profissionais e entusiastas da paleontologia. Por serem reuniões regionais, contribuem para o desenvolvimento de pesquisas através das trocas estabelecidas entre os participantes, além de unir diferentes instituições em prol da ciência. O Boletim Informativo da Sociedade Brasileira de Paleontologia traz todo ano uma compilação dos resumos apresentados nas Paleos como forma de registrar e conservar a memória desses eventos que são tão importantes para a ciência brasileira. -
Massospondylus Carinatus Owen 1854 (Dinosauria: Sauropodomorpha) from the Lower Jurassic of South Africa: Proposed Conservation of Usage by Designation of a Neotype
Massospondylus carinatus Owen 1854 (Dinosauria: Sauropodomorpha) from the Lower Jurassic of South Africa: Proposed conservation of usage by designation of a neotype Adam M. Yates1* & Paul M. Barrett2 1Bernard Price Institute for Palaeontological Research, University of the Witwatersrand, Private Bag 3, WITS, 2050 Johannesburg, South Africa 2Department of Palaeontology, The Natural History Museum, Cromwell Road, London, SW7 5BD, U.K. Received 17 February 2010. Accepted 12 November 2010 The purpose of this article is to preserve the usage of the binomen Massospondylus carinatus by designating a neotype specimen. Massospondylus is the most abundant basal sauropodomorph dinosaur from the Early Jurassic strata of southern Africa. This taxon forms the basis for an extensive palaeobiological literature and is the eponym of Massospondylidae and the nominal taxon of a biostratigraphical unit in current usage, the ‘Massospondylus Range Zone’. The syntype series of M. carinatus (five disarticulated and broken vertebrae) was destroyed during World War II, but plaster casts and illustrations of the material survive. Nonetheless, these materials cannot act as type material for this taxon under the rules of the ICZN Code. In order to avoid nomenclatural instability, we hereby designate BP/1/4934 (a skull and largely complete postcranial skeleton) as the neotype of Massospondylus carinatus. Keywords: Dinosauria, Sauropodomorpha, Massospondylidae, Massospondylus, Massospondylus carinatus, neotype, South Africa, upper Elliot Formation, Early Jurassic. INTRODUCTION same taxon, possibly even the same individual, as at least Richard Owen described and named Massospondylus some of the syntype series of Massospondylus carinatus. carinatus (1854, p. 97) with carinatus as the type species of Their initial separation from Massospondylus carinatus the genus by monotypy. -
Basal Saurischia
TWO Basal Saurischia MAX C. LANGER The name Saurischia was coined by Seeley in lectures given in et al. 1999b; Langer et al. 2000), as well as various strata in the 1887, published in 1888, to designate those dinosaurs possessing western United States and on the Atlantic Coast of both the a propubic pelvis. This plesiomorphic feature distinguishes them United States and Canada (Olsen et al. 1989; Long and Murry from ornithischians, which have an opisthopubic pelvis. De- 1995; Hunt et al. 1998; Lucas 1998). spite its general acceptance as a taxonomic unit since the pro- Interestingly, while saurischian dinosaurs are abundant in posal of the name (Huene 1932; Romer 1956; Colbert 1964a; Steel Carnian strata and became the dominant component of vari- 1970), the monophyly of Saurischia was heavily questioned in ous Norian faunas, ornithischians are barely represented through the 1960s and 1970s (Charig et al. 1965; Charig 1976b; Reig 1970; this time interval. Pisanosaurus mertii, from the Ischigualasto Romer 1972c; Thulborn 1975; Cruickshank 1979). Its status as a Formation, is the sole reasonably well known Triassic member natural group was, however, fixed by Bakker and Galton (1974), of the group, which only achieved higher abundance and di- Bonaparte (1975b) and, more importantly, Gauthier (1986), versity during Early Jurassic times (Weishampel and Norman who formally established the monophyly of the group. 1989). The taxa discussed in this chapter (table 2.1) are usually con- sidered to be among the oldest known dinosaurs. They include the most basal saurischians, as well as various forms of uncer- Definition and Diagnosis tain affinity once assigned to the group. -
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. -
'Big Al'? Quantifying the Effect of Soft
Palaeontologia Electronica http://palaeo-electronica.org HOW BIG WAS ‘BIG AL’? QUANTIFYING THE EFFECT OF SOFT TISSUE AND OSTEOLOGICAL UNKNOWNS ON MASS PREDICTIONS FOR ALLOSAURUS (DINOSAURIA:THEROPODA) Karl T. Bates, Peter L. Falkingham, Brent H. Breithaupt, David Hodgetts, William I. Sellers, and Phillip L. Manning ABSTRACT MOR693, nicknamed ‘Big Al,’ is the most complete skeleton of the non-avian theropod Allosaurus and therefore provides the best opportunity to investigate the mass properties of this important Jurassic theropod through accurate physical or digital volumetric models. In this study, laser scanning and computer modelling software have been used to construct volumetric models of MOR693. A long-range laser scanner has been used to digitize the mounted cast of MOR693, allowing the reconstruction of body volumes and respiratory structures around and within the three-dimensional (3D) skel- etal model. The digital medium offered the facility to modify model properties non- destructively in a detailed sensitivity analysis to quantify the effects of the many unknown parameters involved in such reconstructions. In addition to varying the vol- umes of body segments and respiratory structures, we also extend the sensitivity anal- ysis to include uncertainties regarding osteological articulations in non-avian dinosaurs, including effects of inter-vertebral spacing and the orientation or ‘flare’ of the rib cage in MOR693. Results suggest body mass and inertial values are extremely uncertain and show a wide range in plausible values, whilst the CM (centre of mass) position is well constrained immediately in front and below the hip joint in MOR693, consistent with similar reconstructions of non-avian theropods. Karl T.