Dinosaur-Biodiversity-Reduc

Total Page:16

File Type:pdf, Size:1020Kb

Dinosaur-Biodiversity-Reduc Dinosaur Diversity Changes • During the Mesozoic era, dinosaurs dominated the Top levels of the Food Chain Pyramid • Their ecological territory or “Niche” spread out over many environmental conditions; coastal, fluvial and even desert, almost everywhere on the earth’s surface • Even the sea and air were occupied by closely related reptiles (e.g. Plesiosaurus, Ichthyosaurus, Pteranodon) • Mammals hide from them, so their niches were nocturnal Dinosaur diversity change is important to elucidate future predictions of present-day animal biodiversity. Dinosaur Diversity Changes • During Mesozoic era, dinosaurs dominated the Top levels of the Food Chain Pyramid. • Their ecological territory “Niche” spread out over many environmental conditions; coastal, fluvial and even desert, almost everywhere on the earth’s surface. • Even sea and air occupied by closely related reptiles (e.g. Plesiosaurus, Ichthyosaurus, Pteranodon). • Mammals hide from them, so their niches were nocternal Dinosaur diversity change is important to elucidate future predictions of present-day animal biodiversity. Dinosaur Paleontology Dinosaurs originated in South America • Argentinosaurus is the heaviest dinosaur (length: 30m, weight: 100 tons). • Cretaceous Dinosaur assemblages are different from N. Hemisphere. South America “Sauropoda” North America & Asia “Hadrosaurid” No.1 Dinosaur Kingdom • A large variety of dinosaur fossils • Jurassic dinosaur assemblage is similar to other continents • Diversity of Ceratopsian and Hadrosauridae in late Cretaceous Motherland of Dinosaur Research • Iguanodon is the first Dinosaur specimen and species described . No.2 Dinosaur Kingdom • Recently, Bird-related Dinosaur fossils found. Hatching Oviraptor • Australia was located in polar zone in the early Cretaceous • But there were some dinosaurs (e.g. Muttaburasaurus). New Field of Dinosaur Research • Some dinosaur assemblages are similar to N.&S. America and Europe • It’s good evidence that continents were united (1) Paleogeographic distribution and dinosaur migration • Dinosaur diversity change cannot Late Jurassic really be understood without the influence of Continental drift and dinosaur migration. • Many researchers pointed out the similarity of late Cretaceous dinosaur assemblages between Early Cretaceous the North America and East Asia. • Mongolian dinosaur diversity was affected by migration through the Beringian Isthmus which connected NA and Asia during the Late Cretaceous Late Cretaceous Beringian Isthmus NA Asia NA Asia Europe Europe Early Cretaceous Late Cretaceous Milner et al.(2000) Nemegt Fm. Djadokhta Fm. Bayan Shiree Fm. Upper Cretaceous Lower Cretaceous Location of dinosaur-bearing Cretaceous sections in the Gobi basin Lower Cretaceous General stratigraphic column of the Cretaceous in Mongolia (Jerzykiewicz & Russell, 1991) Early Cretaceous Asiatosaurus mongoliensis Ambiortus dementjevi Harpymimus okladnikovi (sauropoda) Enantiornithes indet. (Ornithomimosauria) Lower (Avialae) Cretaceous Prodeinodon mongoliensis (Theropoda) Shamosaurus scutatus (Ankylosauria) Iguanodon bernissartensis Psittacosaurus Altirhinus kurzanovi mongoliensis Mesozoic stratigraphy mongoliensis (Hadrosauridae) (Neoceratopsia) Baynshirenian “Age” Bayn Shire Fm. Garudimimus brevipes Garudimimus brevipes Achillobator giganticus AlectrosaurusAlectrosaurus olseniolseni (Ornithomimosauria) (Ornithomimosauria) (Dromaeosauridae) (Tyrannosauroidea)(Tyrannosauroidea) Segnosaurus galbiensis Microceratops gobiensis Erlikosaurus andrewsi (Neoceratopsia) Enigmosaurus mongoliensis Sauropoda Gen. Undet. (Therizinosauroidea) Mesozoic stratigraphy Talarurus plicatospineus Bactrosaurus mongoliensis Amtosaurus magnus Arstanosaurus sp. Tsagantegia longicranialis (Hadrosauridae) Maleevus disparoserratus (Ankylosauria) Djadokhta “Age” Djadokhta Fm. Saurornithoides mongoliensis Oviraptor philoceratops Velociraptor mongoliensis Byronosaurus jaffei Citipati osmolskae (Dromaeosauridae) (Troodontidae) Khaan mckennai Ingenia sp. (Oviraptorosauria) ProtoceratopsProtoceratops andrewsiandrewsi UdanoceratopsUdanoceratops tschizhovitschizhovi Sauropoda Gen. Undet. Mononykus olecranus BainoceratopsBainoceratops efremoviefremovi (Avialae) BagaceratopsBagaceratops sp.sp. (Neoceratopsia)(Neoceratopsia) Mesozoic stratigraphy Pinacosaurus grangeri Hadrosauridae Gen. Undet. (Ankylosauria)(Ankylosauria) Barungoyotian “Age” Barun Goyot Fm. Velociraptor sp. Oviraptor philoceratops Tyrannosauroidea indet Hulsanpes perlei Conchoraptor gracilis (Dromaeosauridae) Ingenia yanshini (Oviraptorosauria) Quaesitosaurus orientalis Gobipterix minuta (Diplodocoidea) Parvicursor remotus ProtoceratopsProtoceratops kozlovskiikozlovskii Hesperornithiformes indet. BagaceratopsBagaceratops rozhdestvenskyirozhdestvenskyi (Avialae) LamaceratopsLamaceratops tereschenkoitereschenkoi Mesozoic stratigraphy PlatyceratopsPlatyceratops tatarinovitatarinovi (Neoceratopsia)(Neoceratopsia) Saichania chulsanensis Tarchia gigantea Tylocephale gilmorei (Ankylosauridae) (Pachycephalosauria) Nemegt “Age” Nemegt Fm. Avimimus portentosus Mononykus olecranus Oviraptor mongoliensis Judiornis nogontsavensis Gallimimus bullatus Rinchenia mongoliensis Gurilynia nessovi Tarbosaurus bataar Anserimimus planinychus Nomingia gobiensis Parahesperornis sp. Alioramus remotus Deinocheirus mirificus Elmisaurus rarus Bagaraatan ostromi (Ornithomimosauria) Ingenia yanshini Teviornis gobiensis Gorgosaurus novojilovi (Oviraptorosauria) (Avialae) (Tyrannosauroidea) Adasaurus mongoliensis Therizinosaurus Saurornithoides junior cf.Velociraptor Nemegtosaurus mongoliensis cheloniformis Borogovia gracilicrus (Dromaeosauridae) (Diplodocoidea) (Therizinosauroidea) Tochisaurus nemegtensis Opisthocoelicaudia skarzynskii (Troodontidae) (Sauropoda) Mesozoic stratigraphy Prenocephale prenes Homalocephale calathocercos Saurolophus angustirostris (Pachycephalosauria) Tarchia gigantea Barsboldia sicinskii (Ankylosauria) (Hadrosauridae) Mongolian dinosaur biodiversity change • Ceratopsian Lower Cretaceous: Psittacosaurus appeared & flourished Bayanshiree age: only Microceratops apperared. Djadokhta and Baruungoyot age: Protoceratopsids greatly diversified. • Ankylosauridae Ankylosaurids existed through the Cretaceous, declined at the end • Theropoda Nemegt age: Theropoda flourished. Tarbosaurus (Tyrannosaurid) appeared • Hadrosauridae Nemegt age: Saurolophus (Hadrosaurid) diversified. What makes dinosaur diversity change ?! Comparisons of Late Cretaceous Dinosaurs from Mongolia and North America • Many researchers pointed to the similarity of late Cretaceous dinosaur assemblages in North America and East Asia. Theropoda; Tyrannosauridae Dromaeosauridae Troodontidae Saurornithoidae Oviraptoidae Ornithomimidae Sauropoda; Diplodokcidae Camarasauridae Ornithischia; Neoceratopsidae Ankylosauridae Hadrosauridae Pachycephalosauridae • These dinosaurs’ biodiversity was affected by the migration from Asia to NA. • Differences in dinosaur biodiversity may be affected by environmental differences. NA=coastal, Asia=interior continents Dinosaur assemblage differences in Djadokhta Fm. Ulan Nur Basin • Eolian desert condition (Bayan Zag, Tugrikiin Shiree, Udyn Sayr) … Protoceratops dominated. Dinosaur assemblage differences in Djadokhta Fm. Ulan Nur Basin • Eolian desert condition (Bayan Zag, Tugrikiin Shiree, Udyn Sayr) … Protoceratops dominated. • Fluvial condition (Alag Teeg, Abdrant Nuru, Khongil) … Pinacosaurus dominated. Environmental factor control the dinosaur biodiversity !? Dinosaur assemblage differences in Djadokhta Fm. Ulan Nur Basin • Eolian desert condition (Bayan Zag, Tugrikiin Shiree, Udyn Sayr) … Protoceratops dominated. • Fluvial condition (Alag Teeg, Abdrant Nuru, Khongil) … Pinacosaurus dominated. Environmental factor control the dinosaur biodiversity !? • Stratigraphic correlation of each localities are unclear. • Reconstruction of the paleoenvironment setting at several localities. Paleoenvironmental reconstruction of dinosaur-bearing deposits based on the sedimentological study (2) Environment setting and dinosaur communities • Dinosaur diversity changes cannot really be understood without the influence of the environment setting and dinosaur community • Lehman (1987) identified biogeographic zones in (1) (2) (3) several environments in the latest Cretaceous (1) Leptoceratops: semi-arid region. (2) Triceratops: coastal lowland. (1) Piedmont (semi-arid) (2) Coastal lowland (3) Alamosaurus: alluvial plain • North American dinosaurs (1) have enough rich fauna as (2) supported by sufficient (3) geological studies. (3) Alluvial plain Lehman (1987) .
Recommended publications
  • The Phylogenetic Position of Ambiortus: Comparison with Other Mesozoic Birds from Asia1 J
    ISSN 00310301, Paleontological Journal, 2013, Vol. 47, No. 11, pp. 1270–1281. © Pleiades Publishing, Ltd., 2013. The Phylogenetic Position of Ambiortus: Comparison with Other Mesozoic Birds from Asia1 J. K. O’Connora and N. V. Zelenkovb aKey Laboratory of Evolution and Systematics, Institute of Vertebrate Paleontology and Paleoanthropology, 142 Xizhimenwai Dajie, Beijing China 10044 bBorissiak Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya ul. 123, Moscow, 117997 Russia email: [email protected], [email protected] Received August 6, 2012 Abstract—Since the last description of the ornithurine bird Ambiortus dementjevi from Mongolia, a wealth of Early Cretaceous birds have been discovered in China. Here we provide a detailed comparison of the anatomy of Ambiortus relative to other known Early Cretaceous ornithuromorphs from the Chinese Jehol Group and Xiagou Formation. We include new information on Ambiortus from a previously undescribed slab preserving part of the sternum. Ambiortus is superficially similar to Gansus yumenensis from the Aptian Xiagou Forma tion but shares more morphological features with Yixianornis grabaui (Ornithuromorpha: Songlingorni thidae) from the Jiufotang Formation of the Jehol Group. In general, the mosaic pattern of character distri bution among early ornithuromorph taxa does not reveal obvious relationships between taxa. Ambiortus was placed in a large phylogenetic analysis of Mesozoic birds, which confirms morphological observations and places Ambiortus in a polytomy with Yixianornis and Gansus. Keywords: Ornithuromorpha, Ambiortus, osteology, phylogeny, Early Cretaceous, Mongolia DOI: 10.1134/S0031030113110063 1 INTRODUCTION and articulated partial skeleton, preserving several cervi cal and thoracic vertebrae, and parts of the left thoracic Ambiortus dementjevi Kurochkin, 1982 was one of girdle and wing (specimen PIN, nos.
    [Show full text]
  • A New Troodontid Theropod, Talos Sampsoni Gen. Et Sp. Nov., from the Upper Cretaceous Western Interior Basin of North America
    A New Troodontid Theropod, Talos sampsoni gen. et sp. nov., from the Upper Cretaceous Western Interior Basin of North America Lindsay E. Zanno1,2*, David J. Varricchio3, Patrick M. O’Connor4,5, Alan L. Titus6, Michael J. Knell3 1 Field Museum of Natural History, Chicago, Illinois, United States of America, 2 Biological Sciences Department, University of Wisconsin-Parkside, Kenosha, Wisconsin, United States of America, 3 Department of Earth Sciences, Montana State University, Bozeman, Montana, United States of America, 4 Department of Biomedical Sciences, Ohio University College of Osteopathic Medicine, Athens, Ohio, United States of America, 5 Ohio Center for Ecology and Evolutionary Studies, Ohio University, Athens, Ohio, United States of America, 6 Grand Staircase-Escalante National Monument, Bureau of Land Management, Kanab, Utah, United States of America Abstract Background: Troodontids are a predominantly small-bodied group of feathered theropod dinosaurs notable for their close evolutionary relationship with Avialae. Despite a diverse Asian representation with remarkable growth in recent years, the North American record of the clade remains poor, with only one controversial species—Troodon formosus—presently known from substantial skeletal remains. Methodology/Principal Findings: Here we report a gracile new troodontid theropod—Talos sampsoni gen. et sp. nov.— from the Upper Cretaceous Kaiparowits Formation, Utah, USA, representing one of the most complete troodontid skeletons described from North America to date. Histological assessment of the holotype specimen indicates that the adult body size of Talos was notably smaller than that of the contemporary genus Troodon. Phylogenetic analysis recovers Talos as a member of a derived, latest Cretaceous subclade, minimally containing Troodon, Saurornithoides, and Zanabazar.
    [Show full text]
  • PALEONTOLOGY and BIOSTRATIGRAPHY of MONGOLIA the JOINT SOVIET-MONGOLIAN PALEONTOLOGICAL EXPEDITION (Transactions, Vol
    PALEONTOLOGY AND BIOSTRATIGRAPHY OF MONGOLIA THE JOINT SOVIET-MONGOLIAN PALEONTOLOGICAL EXPEDITION (Transactions, vol. 3) EDITORIAL BOARD: N. N. Kramarenko (editor-in-chief) B. Luvsandansan, Yu. I. Voronin, R. Barsbold, A. K. Rozhdestvensky, B. A. Trofimov, V. Yu. Reshetov 1976 S. M. Kurzanov A NEW CARNOSAUR FROM THE LATE CRETACEOUS OF NOGON-TSAV, MONGOLIA* The Upper Cretaceous locality of Nogon-Tsav, located in the Zaltaika Gobi, 20 km NW of Mt. Ongon-Ulan-Ula, was discovered by geologists of the MNR. Then, in a series of years (1969–1971, 1973) the joint Soviet-Mongolian Geological Expedition investigated the site. According to the oral report of B. Yu. Reshetova, the deposits in this region are composed basically of sandstone and clay, clearly subdivided into two deposits. The lower great thickness contains many complete skulls, separate bones of tarbosaurs, ornithomimids, and claws of therizinosaurs. The upper red-colored beds are characterized only by scattered fragments of skulls. The fragments described below are of a new carnivorous dinosaur, Alioramus remotus (coll. South Goby region), from the family Tyrannosauridae, which occurs in the lower gray beds. Genus Alioramus Kurzanov, gen. nov. G e n u s n a m e from alius (Lat.) – other, ramus (Lat.) – branch; masc. G e n o t y p e — A. remotus Kurzanov, sp. nov., Upper Cretaceous, Nemegetinskaya suite, southern Mongolia. D i a g n o s i s . Tyrannosaurid of average size. Skull low, with highly elongated jaws. Nasals with well-developed separate crests of 1–l.5 cm height. Second antorbital fenestrae displaced forward, reaching the anterior end of the 5th tooth.
    [Show full text]
  • A Revised Taxonomy of the Iguanodont Dinosaur Genera and Species
    ARTICLE IN PRESS + MODEL Cretaceous Research xx (2007) 1e25 www.elsevier.com/locate/CretRes A revised taxonomy of the iguanodont dinosaur genera and species Gregory S. Paul 3109 North Calvert Station, Side Apartment, Baltimore, MD 21218-3807, USA Received 20 April 2006; accepted in revised form 27 April 2007 Abstract Criteria for designating dinosaur genera are inconsistent; some very similar species are highly split at the generic level, other anatomically disparate species are united at the same rank. Since the mid-1800s the classic genus Iguanodon has become a taxonomic grab-bag containing species spanning most of the Early Cretaceous of the northern hemisphere. Recently the genus was radically redesignated when the type was shifted from nondiagnostic English Valanginian teeth to a complete skull and skeleton of the heavily built, semi-quadrupedal I. bernissartensis from much younger Belgian sediments, even though the latter is very different in form from the gracile skeletal remains described by Mantell. Currently, iguanodont remains from Europe are usually assigned to either robust I. bernissartensis or gracile I. atherfieldensis, regardless of lo- cation or stage. A stratigraphic analysis is combined with a character census that shows the European iguanodonts are markedly more morpho- logically divergent than other dinosaur genera, and some appear phylogenetically more derived than others. Two new genera and a new species have been or are named for the gracile iguanodonts of the Wealden Supergroup; strongly bipedal Mantellisaurus atherfieldensis Paul (2006. Turning the old into the new: a separate genus for the gracile iguanodont from the Wealden of England. In: Carpenter, K. (Ed.), Horns and Beaks: Ceratopsian and Ornithopod Dinosaurs.
    [Show full text]
  • Was Dinosaurian Physiology Inherited by Birds? Reconciling Slow Growth in Archaeopteryx
    Was Dinosaurian Physiology Inherited by Birds? Reconciling Slow Growth in Archaeopteryx Gregory M. Erickson1,6*, Oliver W. M. Rauhut2, Zhonghe Zhou3, Alan H. Turner4,6, Brian D. Inouye1, Dongyu Hu5, Mark A. Norell6 1 Department of Biological Science, Florida State University, Tallahassee, Florida, United States of America, 2 Bayerische Staatssammlung fu¨r Pala¨ontologie und Geologie and Department of Earth and Environmental Sciences, LMU Munich, Mu¨nchen, Germany, 3 Key Laboratory of Evolutionary Systematics of Vertebrates, Institute of Vertebrate Paleontology & Paleoanthropology, Chinese Academy of Science, Beijing, China, 4 Department of Anatomical Sciences, Stony Brook University, Stony Brook, New York, United States of America, 5 Paleontological Institute, Shenyang Normal University, Shenyang, China, 6 Division of Paleontology, American Museum of Natural History, New York, New York, United States of America Abstract Background: Archaeopteryx is the oldest and most primitive known bird (Avialae). It is believed that the growth and energetic physiology of basalmost birds such as Archaeopteryx were inherited in their entirety from non-avialan dinosaurs. This hypothesis predicts that the long bones in these birds formed using rapidly growing, well-vascularized woven tissue typical of non-avialan dinosaurs. Methodology/Principal Findings: We report that Archaeopteryx long bones are composed of nearly avascular parallel- fibered bone. This is among the slowest growing osseous tissues and is common in ectothermic reptiles. These findings dispute the hypothesis that non-avialan dinosaur growth and physiology were inherited in totality by the first birds. Examining these findings in a phylogenetic context required intensive sampling of outgroup dinosaurs and basalmost birds. Our results demonstrate the presence of a scale-dependent maniraptoran histological continuum that Archaeopteryx and other basalmost birds follow.
    [Show full text]
  • Perinate and Eggs of a Giant Caenagnathid Dinosaur from the Late Cretaceous of Central China
    ARTICLE Received 29 Jul 2016 | Accepted 15 Feb 2017 | Published 9 May 2017 DOI: 10.1038/ncomms14952 OPEN Perinate and eggs of a giant caenagnathid dinosaur from the Late Cretaceous of central China Hanyong Pu1, Darla K. Zelenitsky2, Junchang Lu¨3, Philip J. Currie4, Kenneth Carpenter5,LiXu1, Eva B. Koppelhus4, Songhai Jia1, Le Xiao1, Huali Chuang1, Tianran Li1, Martin Kundra´t6 & Caizhi Shen3 The abundance of dinosaur eggs in Upper Cretaceous strata of Henan Province, China led to the collection and export of countless such fossils. One of these specimens, recently repatriated to China, is a partial clutch of large dinosaur eggs (Macroelongatoolithus) with a closely associated small theropod skeleton. Here we identify the specimen as an embryo and eggs of a new, large caenagnathid oviraptorosaur, Beibeilong sinensis. This specimen is the first known association between skeletal remains and eggs of caenagnathids. Caenagnathids and oviraptorids share similarities in their eggs and clutches, although the eggs of Beibeilong are significantly larger than those of oviraptorids and indicate an adult body size comparable to a gigantic caenagnathid. An abundance of Macroelongatoolithus eggs reported from Asia and North America contrasts with the dearth of giant caenagnathid skeletal remains. Regardless, the large caenagnathid-Macroelongatoolithus association revealed here suggests these dinosaurs were relatively common during the early Late Cretaceous. 1 Henan Geological Museum, Zhengzhou 450016, China. 2 Department of Geoscience, University of Calgary, Calgary, Alberta, Canada T2N 1N4. 3 Institute of Geology, Chinese Academy of Geological Sciences, Beijing 100037, China. 4 Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9. 5 Prehistoric Museum, Utah State University, 155 East Main Street, Price, Utah 84501, USA.
    [Show full text]
  • Onetouch 4.0 Scanned Documents
    / Chapter 2 THE FOSSIL RECORD OF BIRDS Storrs L. Olson Department of Vertebrate Zoology National Museum of Natural History Smithsonian Institution Washington, DC. I. Introduction 80 II. Archaeopteryx 85 III. Early Cretaceous Birds 87 IV. Hesperornithiformes 89 V. Ichthyornithiformes 91 VI. Other Mesozojc Birds 92 VII. Paleognathous Birds 96 A. The Problem of the Origins of Paleognathous Birds 96 B. The Fossil Record of Paleognathous Birds 104 VIII. The "Basal" Land Bird Assemblage 107 A. Opisthocomidae 109 B. Musophagidae 109 C. Cuculidae HO D. Falconidae HI E. Sagittariidae 112 F. Accipitridae 112 G. Pandionidae 114 H. Galliformes 114 1. Family Incertae Sedis Turnicidae 119 J. Columbiformes 119 K. Psittaciforines 120 L. Family Incertae Sedis Zygodactylidae 121 IX. The "Higher" Land Bird Assemblage 122 A. Coliiformes 124 B. Coraciiformes (Including Trogonidae and Galbulae) 124 C. Strigiformes 129 D. Caprimulgiformes 132 E. Apodiformes 134 F. Family Incertae Sedis Trochilidae 135 G. Order Incertae Sedis Bucerotiformes (Including Upupae) 136 H. Piciformes 138 I. Passeriformes 139 X. The Water Bird Assemblage 141 A. Gruiformes 142 B. Family Incertae Sedis Ardeidae 165 79 Avian Biology, Vol. Vlll ISBN 0-12-249408-3 80 STORES L. OLSON C. Family Incertae Sedis Podicipedidae 168 D. Charadriiformes 169 E. Anseriformes 186 F. Ciconiiformes 188 G. Pelecaniformes 192 H. Procellariiformes 208 I. Gaviiformes 212 J. Sphenisciformes 217 XI. Conclusion 217 References 218 I. Introduction Avian paleontology has long been a poor stepsister to its mammalian counterpart, a fact that may be attributed in some measure to an insufRcien- cy of qualified workers and to the absence in birds of heterodont teeth, on which the greater proportion of the fossil record of mammals is founded.
    [Show full text]
  • A New Caenagnathid Dinosaur from the Upper Cretaceous Wangshi
    www.nature.com/scientificreports OPEN A new caenagnathid dinosaur from the Upper Cretaceous Wangshi Group of Shandong, China, with Received: 12 October 2017 Accepted: 7 March 2018 comments on size variation among Published: xx xx xxxx oviraptorosaurs Yilun Yu1, Kebai Wang2, Shuqing Chen2, Corwin Sullivan3,4, Shuo Wang 5,6, Peiye Wang2 & Xing Xu7 The bone-beds of the Upper Cretaceous Wangshi Group in Zhucheng, Shandong, China are rich in fossil remains of the gigantic hadrosaurid Shantungosaurus. Here we report a new oviraptorosaur, Anomalipes zhaoi gen. et sp. nov., based on a recently collected specimen comprising a partial left hindlimb from the Kugou Locality in Zhucheng. This specimen’s systematic position was assessed by three numerical cladistic analyses based on recently published theropod phylogenetic datasets, with the inclusion of several new characters. Anomalipes zhaoi difers from other known caenagnathids in having a unique combination of features: femoral head anteroposteriorly narrow and with signifcant posterior orientation; accessory trochanter low and confuent with lesser trochanter; lateral ridge present on femoral lateral surface; weak fourth trochanter present; metatarsal III with triangular proximal articular surface, prominent anterior fange near proximal end, highly asymmetrical hemicondyles, and longitudinal groove on distal articular surface; and ungual of pedal digit II with lateral collateral groove deeper and more dorsally located than medial groove. The holotype of Anomalipes zhaoi is smaller than is typical for Caenagnathidae but larger than is typical for the other major oviraptorosaurian subclade, Oviraptoridae. Size comparisons among oviraptorisaurians show that the Caenagnathidae vary much more widely in size than the Oviraptoridae. Oviraptorosauria is a clade of maniraptoran theropod dinosaurs characterized by a short, high skull, long neck and short tail.
    [Show full text]
  • New Oviraptorid Dinosaur (Dinosauria: Oviraptorosauria) from the Nemegt Formation of Southwestern Mongolia
    Bull. Natn. Sci. Mus., Tokyo, Ser. C, 30, pp. 95–130, December 22, 2004 New Oviraptorid Dinosaur (Dinosauria: Oviraptorosauria) from the Nemegt Formation of Southwestern Mongolia Junchang Lü1, Yukimitsu Tomida2, Yoichi Azuma3, Zhiming Dong4 and Yuong-Nam Lee5 1 Institute of Geology, Chinese Academy of Geological Sciences, Beijing 100037, China 2 National Science Museum, 3–23–1 Hyakunincho, Shinjukuku, Tokyo 169–0073, Japan 3 Fukui Prefectural Dinosaur Museum, 51–11 Terao, Muroko, Katsuyama 911–8601, Japan 4 Institute of Paleontology and Paleoanthropology, Chinese Academy of Sciences, Beijing 100044, China 5 Korea Institute of Geoscience and Mineral Resources, Geology & Geoinformation Division, 30 Gajeong-dong, Yuseong-gu, Daejeon 305–350, South Korea Abstract Nemegtia barsboldi gen. et sp. nov. here described is a new oviraptorid dinosaur from the Late Cretaceous (mid-Maastrichtian) Nemegt Formation of southwestern Mongolia. It differs from other oviraptorids in the skull having a well-developed crest, the anterior margin of which is nearly vertical, and the dorsal margin of the skull and the anterior margin of the crest form nearly 90°; the nasal process of the premaxilla being less exposed on the dorsal surface of the skull than those in other known oviraptorids; the length of the frontal being approximately one fourth that of the parietal along the midline of the skull. Phylogenetic analysis shows that Nemegtia barsboldi is more closely related to Citipati osmolskae than to any other oviraptorosaurs. Key words : Nemegt Basin, Mongolia, Nemegt Formation, Late Cretaceous, Oviraptorosauria, Nemegtia. dae, and Caudipterygidae (Barsbold, 1976; Stern- Introduction berg, 1940; Currie, 2000; Clark et al., 2001; Ji et Oviraptorosaurs are generally regarded as non- al., 1998; Zhou and Wang, 2000; Zhou et al., avian theropod dinosaurs (Osborn, 1924; Bars- 2000).
    [Show full text]
  • Velociraptor Guide
    Ages 7 & up EI-5179 Guide Book VELOCIRAPTOR Ages 7 & up EI-5176 Ages 7 & up EI-5177 Ages 7 & up EI-5178 Dig ‘em up Dig ‘em up Dig ‘em up ‘em Assemble Assemble ‘em Assemble ‘em uel ‘em l ‘em Collect & d Collect & due Collect & duel ‘em nosaur ntai ns one d i one d inosaur Kit co Kit contai ns ne d inosaur Kit contai ns o TYRANNOSAURUS TRICERATOPS STEGOSAURUSSTEGOSAURUS EI-5176 EI-5177 EI-5178 For more digging fun, add these Dueling Dino Dig kits to your collection! ™ ISBN 1-56767-219-1 Table of Contents What Is in Dueling Dino Dig?. 2 Welcome to Velociraptor’s World . 4 Attack of a Velociraptor Pack . 5 Velociraptor Findings . 10 A Dinosaur Dig . 12 You’ll DIG These Fossils! . 14 Get Ready to Dig . 16 Dino Drawing . 18 Draw Your Own . 18 Velociraptor Fact Sheet . 20 Picture Gallery . 21 Making Your Velociraptor Models . 22 Displaying Your Velociraptors . 24 © Copyright 1997 Educational Insights Inc., Carson, CA (USA), St Albans, Herts. (UK) All rights reserved. Please retain this information. The Age of Dinosaurs . 26 Conforms to ASTM F-963-96a, EN-71. Printed in China. EI-5179 Where Did They Go? . 29 1 Paleontologist’s tools: What Is in Dueling Just like a paleontologist, you will get to dig the “fossils” from the “earth.” The digging tool Dino Dig? will help you break apart the clay, separate the fossils from the clay, and clean bits of clay from the fossils. The brush Dueling Dino Dig Guide Book—Velociraptor kit: will let you clean the dust from the fossils as you excavate.
    [Show full text]
  • Implications for Predatory Dinosaur Macroecology and Ontogeny in Later Late Cretaceous Asiamerica
    Canadian Journal of Earth Sciences Theropod Guild Structure and the Tyrannosaurid Niche Assimilation Hypothesis: Implications for Predatory Dinosaur Macroecology and Ontogeny in later Late Cretaceous Asiamerica Journal: Canadian Journal of Earth Sciences Manuscript ID cjes-2020-0174.R1 Manuscript Type: Article Date Submitted by the 04-Jan-2021 Author: Complete List of Authors: Holtz, Thomas; University of Maryland at College Park, Department of Geology; NationalDraft Museum of Natural History, Department of Geology Keyword: Dinosaur, Ontogeny, Theropod, Paleocology, Mesozoic, Tyrannosauridae Is the invited manuscript for consideration in a Special Tribute to Dale Russell Issue? : © The Author(s) or their Institution(s) Page 1 of 91 Canadian Journal of Earth Sciences 1 Theropod Guild Structure and the Tyrannosaurid Niche Assimilation Hypothesis: 2 Implications for Predatory Dinosaur Macroecology and Ontogeny in later Late Cretaceous 3 Asiamerica 4 5 6 Thomas R. Holtz, Jr. 7 8 Department of Geology, University of Maryland, College Park, MD 20742 USA 9 Department of Paleobiology, National Museum of Natural History, Washington, DC 20013 USA 10 Email address: [email protected] 11 ORCID: 0000-0002-2906-4900 Draft 12 13 Thomas R. Holtz, Jr. 14 Department of Geology 15 8000 Regents Drive 16 University of Maryland 17 College Park, MD 20742 18 USA 19 Phone: 1-301-405-4084 20 Fax: 1-301-314-9661 21 Email address: [email protected] 22 23 1 © The Author(s) or their Institution(s) Canadian Journal of Earth Sciences Page 2 of 91 24 ABSTRACT 25 Well-sampled dinosaur communities from the Jurassic through the early Late Cretaceous show 26 greater taxonomic diversity among larger (>50kg) theropod taxa than communities of the 27 Campano-Maastrichtian, particularly to those of eastern/central Asia and Laramidia.
    [Show full text]
  • Appendix A. Supplementary Material
    Appendix A. Supplementary material Comprehensive taxon sampling and vetted fossils help clarify the time tree of shorebirds (Aves, Charadriiformes) David Cernˇ y´ 1,* & Rossy Natale2 1Department of the Geophysical Sciences, University of Chicago, Chicago 60637, USA 2Department of Organismal Biology & Anatomy, University of Chicago, Chicago 60637, USA *Corresponding Author. Email: [email protected] Contents 1 Fossil Calibrations 2 1.1 Calibrations used . .2 1.2 Rejected calibrations . 22 2 Outgroup sequences 30 2.1 Neornithine outgroups . 33 2.2 Non-neornithine outgroups . 39 3 Supplementary Methods 72 4 Supplementary Figures and Tables 74 5 Image Credits 91 References 99 1 1 Fossil Calibrations 1.1 Calibrations used Calibration 1 Node calibrated. MRCA of Uria aalge and Uria lomvia. Fossil taxon. Uria lomvia (Linnaeus, 1758). Specimen. CASG 71892 (referred specimen; Olson, 2013), California Academy of Sciences, San Francisco, CA, USA. Lower bound. 2.58 Ma. Phylogenetic justification. As in Smith (2015). Age justification. The status of CASG 71892 as the oldest known record of either of the two spp. of Uria was recently confirmed by the review of Watanabe et al. (2016). The younger of the two marine transgressions at the Tolstoi Point corresponds to the Bigbendian transgression (Olson, 2013), which contains the Gauss-Matuyama magnetostratigraphic boundary (Kaufman and Brigham-Grette, 1993). Attempts to date this reversal have been recently reviewed by Ohno et al. (2012); Singer (2014), and Head (2019). In particular, Deino et al. (2006) were able to tightly bracket the age of the reversal using high-precision 40Ar/39Ar dating of two tuffs in normally and reversely magnetized lacustrine sediments from Kenya, obtaining a value of 2.589 ± 0.003 Ma.
    [Show full text]