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Annotated Checklist of Fossil Fishes from the Smoky Hill Chalk of the Niobrara Chalk (Upper Cretaceous) in Kansas
Lucas, S. G. and Sullivan, R.M., eds., 2006, Late Cretaceous vertebrates from the Western Interior. New Mexico Museum of Natural History and Science Bulletin 35. 193 ANNOTATED CHECKLIST OF FOSSIL FISHES FROM THE SMOKY HILL CHALK OF THE NIOBRARA CHALK (UPPER CRETACEOUS) IN KANSAS KENSHU SHIMADA1 AND CHRISTOPHER FIELITZ2 1Environmental Science Program and Department of Biological Sciences, DePaul University,2325 North Clifton Avenue, Chicago, Illinois 60614; and Sternberg Museum of Natural History, Fort Hays State University, 3000 Sternberg Drive, Hays, Kansas 67601;2Department of Biology, Emory & Henry College, P.O. Box 947, Emory, Virginia 24327 Abstract—The Smoky Hill Chalk Member of the Niobrara Chalk is an Upper Cretaceous marine deposit found in Kansas and adjacent states in North America. The rock, which was formed under the Western Interior Sea, has a long history of yielding spectacular fossil marine vertebrates, including fishes. Here, we present an annotated taxo- nomic list of fossil fishes (= non-tetrapod vertebrates) described from the Smoky Hill Chalk based on published records. Our study shows that there are a total of 643 referable paleoichthyological specimens from the Smoky Hill Chalk documented in literature of which 133 belong to chondrichthyans and 510 to osteichthyans. These 643 specimens support the occurrence of a minimum of 70 species, comprising at least 16 chondrichthyans and 54 osteichthyans. Of these 70 species, 44 are represented by type specimens from the Smoky Hill Chalk. However, it must be noted that the fossil record of Niobrara fishes shows evidence of preservation, collecting, and research biases, and that the paleofauna is a time-averaged assemblage over five million years of chalk deposition. -
Asteroid Impact, Not Volcanism, Caused the End-Cretaceous Dinosaur Extinction
Asteroid impact, not volcanism, caused the end-Cretaceous dinosaur extinction Alfio Alessandro Chiarenzaa,b,1,2, Alexander Farnsworthc,1, Philip D. Mannionb, Daniel J. Luntc, Paul J. Valdesc, Joanna V. Morgana, and Peter A. Allisona aDepartment of Earth Science and Engineering, Imperial College London, South Kensington, SW7 2AZ London, United Kingdom; bDepartment of Earth Sciences, University College London, WC1E 6BT London, United Kingdom; and cSchool of Geographical Sciences, University of Bristol, BS8 1TH Bristol, United Kingdom Edited by Nils Chr. Stenseth, University of Oslo, Oslo, Norway, and approved May 21, 2020 (received for review April 1, 2020) The Cretaceous/Paleogene mass extinction, 66 Ma, included the (17). However, the timing and size of each eruptive event are demise of non-avian dinosaurs. Intense debate has focused on the highly contentious in relation to the mass extinction event (8–10). relative roles of Deccan volcanism and the Chicxulub asteroid im- An asteroid, ∼10 km in diameter, impacted at Chicxulub, in pact as kill mechanisms for this event. Here, we combine fossil- the present-day Gulf of Mexico, 66 Ma (4, 18, 19), leaving a crater occurrence data with paleoclimate and habitat suitability models ∼180 to 200 km in diameter (Fig. 1A). This impactor struck car- to evaluate dinosaur habitability in the wake of various asteroid bonate and sulfate-rich sediments, leading to the ejection and impact and Deccan volcanism scenarios. Asteroid impact models global dispersal of large quantities of dust, ash, sulfur, and other generate a prolonged cold winter that suppresses potential global aerosols into the atmosphere (4, 18–20). These atmospheric dinosaur habitats. -
Cambridge University Press 978-1-107-17944-8 — Evolution And
Cambridge University Press 978-1-107-17944-8 — Evolution and Development of Fishes Edited by Zerina Johanson , Charlie Underwood , Martha Richter Index More Information Index abaxial muscle,33 Alizarin red, 110 arandaspids, 5, 61–62 abdominal muscles, 212 Alizarin red S whole mount staining, 127 Arandaspis, 5, 61, 69, 147 ability to repair fractures, 129 Allenypterus, 253 arcocentra, 192 Acanthodes, 14, 79, 83, 89–90, 104, 105–107, allometric growth, 129 Arctic char, 130 123, 152, 152, 156, 213, 221, 226 alveolar bone, 134 arcualia, 4, 49, 115, 146, 191, 206 Acanthodians, 3, 7, 13–15, 18, 23, 29, 63–65, Alx, 36, 47 areolar calcification, 114 68–69, 75, 79, 82, 84, 87–89, 91, 99, 102, Amdeh Formation, 61 areolar cartilage, 192 104–106, 114, 123, 148–149, 152–153, ameloblasts, 134 areolar mineralisation, 113 156, 160, 189, 192, 195, 198–199, 207, Amia, 154, 185, 190, 193, 258 Areyongalepis,7,64–65 213, 217–218, 220 ammocoete, 30, 40, 51, 56–57, 176, 206, 208, Argentina, 60–61, 67 Acanthodiformes, 14, 68 218 armoured agnathans, 150 Acanthodii, 152 amphiaspids, 5, 27 Arthrodira, 12, 24, 26, 28, 74, 82–84, 86, 194, Acanthomorpha, 20 amphibians, 1, 20, 150, 172, 180–182, 245, 248, 209, 222 Acanthostega, 22, 155–156, 255–258, 260 255–256 arthrodires, 7, 11–13, 22, 28, 71–72, 74–75, Acanthothoraci, 24, 74, 83 amphioxus, 49, 54–55, 124, 145, 155, 157, 159, 80–84, 152, 192, 207, 209, 212–213, 215, Acanthothoracida, 11 206, 224, 243–244, 249–250 219–220 acanthothoracids, 7, 12, 74, 81–82, 211, 215, Amphioxus, 120 Ascl,36 219 Amphystylic, 148 Asiaceratodus,21 -
Estimating the Evolutionary Rates in Mosasauroids and Plesiosaurs: Discussion of Niche Occupation in Late Cretaceous Seas
Estimating the evolutionary rates in mosasauroids and plesiosaurs: discussion of niche occupation in Late Cretaceous seas Daniel Madzia1 and Andrea Cau2 1 Department of Evolutionary Paleobiology, Institute of Paleobiology, Polish Academy of Sciences, Warsaw, Poland 2 Independent, Parma, Italy ABSTRACT Observations of temporal overlap of niche occupation among Late Cretaceous marine amniotes suggest that the rise and diversification of mosasauroid squamates might have been influenced by competition with or disappearance of some plesiosaur taxa. We discuss that hypothesis through comparisons of the rates of morphological evolution of mosasauroids throughout their evolutionary history with those inferred for contemporary plesiosaur clades. We used expanded versions of two species- level phylogenetic datasets of both these groups, updated them with stratigraphic information, and analyzed using the Bayesian inference to estimate the rates of divergence for each clade. The oscillations in evolutionary rates of the mosasauroid and plesiosaur lineages that overlapped in time and space were then used as a baseline for discussion and comparisons of traits that can affect the shape of the niche structures of aquatic amniotes, such as tooth morphologies, body size, swimming abilities, metabolism, and reproduction. Only two groups of plesiosaurs are considered to be possible niche competitors of mosasauroids: the brachauchenine pliosaurids and the polycotylid leptocleidians. However, direct evidence for interactions between mosasauroids and plesiosaurs is scarce and limited only to large mosasauroids as the Submitted 31 July 2019 predators/scavengers and polycotylids as their prey. The first mosasauroids differed Accepted 18 March 2020 from contemporary plesiosaurs in certain aspects of all discussed traits and no evidence Published 13 April 2020 suggests that early representatives of Mosasauroidea diversified after competitions with Corresponding author plesiosaurs. -
35-51 New Data on Pleuropholis Decastroi (Teleostei, Pleuropholidae)
Geo-Eco-Trop., 2019, 43, 1 : 35-51 New data on Pleuropholis decastroi (Teleostei, Pleuropholidae), a “pholidophoriform” fish from the Lower Cretaceous of the Eurafrican Mesogea Nouvelles données sur Pleuropholis decastroi (Teleostei, Pleuropholidae), un poisson “pholidophoriforme” du Crétacé inférieur de la Mésogée eurafricaine Louis TAVERNE 1 & Luigi CAPASSO 2 Résumé: Le crâne et le corps de Pleuropholis decastroi, un poisson fossile de l’Albien (Crétacé inférieur) du sud de l’Italie, sont redécrits en détails. P. decastroi diffère des autres espèces du genre par ses deux nasaux en contact médian et qui séparent complètement le dermethmoïde ( = rostral) des frontaux. Avec son maxillaire extrêmement élargi qui couvre la mâchoire inférieure et son supramaxillaire fortement réduit, P. decastroi semble plus nettement apparenté avec Pleuropholis cisnerosorum, du Jurassique supérieur du Mexique, qu’avec les autres espèces du genre. Par ses mâchoires raccourcies et ses nombreux os orbitaires, Pleuropholis apparaît également comme le genre le plus spécialisé de la famille. La position systématique des Pleuropholidae au sein du groupe des « pholidophoriformes » est discutée. Mots-clés: Pleuropholis decastroi, Albien, Italie du sud, Pleuropholis, Pleuropholidae, “Pholidophoriformes”, ostéologie, position systématique. Abstract: The skull and the body of Pleuropholis decastroi, a fossil fish from the marine Albian (Lower Cretaceous) of southern Italy, are re-described in details. P. decastroi differs from the other species of the genus by their two nasals that are in contact along the mid-line, completely separating the dermethmoid (= rostral) from the frontals. With its extremely broadened maxilla that covers the lower jaw and its strongly reduced supramaxilla, P. decastroi seems more closely related to Pleuropholis cisnerosorum, from the Upper Jurassic of Mexico, than to the other species of the genus. -
A Revision of the Classification of the Plesiosauria with a Synopsis of the Stratigraphical and Geographical Distribution Of
LUNDS UNIVERSITETS ARSSKRIFT. N. F. Avd. 2. Bd 59. Nr l. KUNGL. FYSIOGRAFISKA SÅLLSKAPETS HANDLINGAR, N. F. Bd 74. Nr 1. A REVISION OF THE CLASSIFICATION OF THE PLESIOSAURIA WITH A SYNOPSIS OF THE STRATIGRAPHICAL AND GEOGRAPHICAL DISTRIBUTION OF THE GROUP BY PER OVE PERSSON LUND C. W. K. GLEER UP Read before the Royal Physiographic Society, February 13, 1963. LUND HÅKAN OHLSSONS BOKTRYCKERI l 9 6 3 l. Introduction The sub-order Plesiosauria is one of the best known of the Mesozoic Reptile groups, but, as emphasized by KuHN (1961, p. 75) and other authors, its classification is still not satisfactory, and needs a thorough revision. The present paper is an attempt at such a revision, and includes also a tabular synopsis of the stratigraphical and geo graphical distribution of the group. Some of the species are discussed in the text (pp. 17-22). The synopsis is completed with seven maps (figs. 2-8, pp. 10-16), a selective synonym list (pp. 41-42), and a list of rejected species (pp. 42-43). Some forms which have been erroneously referred to the Plesiosauria are also briefly mentioned ("Non-Plesiosaurians", p. 43). - The numerals in braekets after the generic and specific names in the text refer to the tabular synopsis, in which the different forms are numbered in successional order. The author has exaroined all material available from Sweden, Australia and Spitzbergen (PERSSON 1954, 1959, 1960, 1962, 1962a); the major part of the material from the British Isles, France, Belgium and Luxembourg; some of the German spec imens; certain specimens from New Zealand, now in the British Museum (see LYDEK KER 1889, pp. -
Marine Reptiles
Species group report card – marine reptiles Supporting the marine bioregional plan for the North Marine Region prepared under the Environment Protection and Biodiversity Conservation Act 1999 Disclaimer © Commonwealth of Australia 2012 This work is copyright. Apart from any use as permitted under the Copyright Act 1968, no part may be reproduced by any process without prior written permission from the Commonwealth. Requests and enquiries concerning reproduction and rights should be addressed to Department of Sustainability, Environment, Water, Population and Communities, Public Affairs, GPO Box 787 Canberra ACT 2601 or email [email protected] Images: A gorgonian wtih polyps extended – Geoscience Australia, Hawksbill Turtle – Paradise Ink, Crested Tern fishing – R.Freeman, Hard corals – A.Heyward and M.Rees, Morning Light – I.Kiessling, Soft corals – A.Heyward and M.Rees, Snubfin Dolphin – D.Thiele, Shrimp, scampi and brittlestars – A.Heyward and M.Rees, Freshwater sawfish – R.Pillans, CSIRO Marine and Atmospheric Research, Yellowstripe Snapper – Robert Thorn and DSEWPaC ii | Supporting the marine bioregional plan for the North Marine Region | Species group report card – marine reptiles CONTENTS Species group report card – marine reptiles ..........................................................................1 1. Marine reptiles of the North Marine Region .............................................................................3 2. Vulnerabilities and pressures ................................................................................................ -
The Geologic Time Scale Is the Eon
Exploring Geologic Time Poster Illustrated Teacher's Guide #35-1145 Paper #35-1146 Laminated Background Geologic Time Scale Basics The history of the Earth covers a vast expanse of time, so scientists divide it into smaller sections that are associ- ated with particular events that have occurred in the past.The approximate time range of each time span is shown on the poster.The largest time span of the geologic time scale is the eon. It is an indefinitely long period of time that contains at least two eras. Geologic time is divided into two eons.The more ancient eon is called the Precambrian, and the more recent is the Phanerozoic. Each eon is subdivided into smaller spans called eras.The Precambrian eon is divided from most ancient into the Hadean era, Archean era, and Proterozoic era. See Figure 1. Precambrian Eon Proterozoic Era 2500 - 550 million years ago Archaean Era 3800 - 2500 million years ago Hadean Era 4600 - 3800 million years ago Figure 1. Eras of the Precambrian Eon Single-celled and simple multicelled organisms first developed during the Precambrian eon. There are many fos- sils from this time because the sea-dwelling creatures were trapped in sediments and preserved. The Phanerozoic eon is subdivided into three eras – the Paleozoic era, Mesozoic era, and Cenozoic era. An era is often divided into several smaller time spans called periods. For example, the Paleozoic era is divided into the Cambrian, Ordovician, Silurian, Devonian, Carboniferous,and Permian periods. Paleozoic Era Permian Period 300 - 250 million years ago Carboniferous Period 350 - 300 million years ago Devonian Period 400 - 350 million years ago Silurian Period 450 - 400 million years ago Ordovician Period 500 - 450 million years ago Cambrian Period 550 - 500 million years ago Figure 2. -
A New Plesiosaur from the Lower Jurassic of Portugal and the Early Radiation of Plesiosauroidea
A new plesiosaur from the Lower Jurassic of Portugal and the early radiation of Plesiosauroidea EDUARDO PUÉRTOLAS-PASCUAL, MIGUEL MARX, OCTÁVIO MATEUS, ANDRÉ SALEIRO, ALEXANDRA E. FERNANDES, JOÃO MARINHEIRO, CARLA TOMÁS, and SIMÃO MATEUS Puértolas-Pascual, E., Marx, M., Mateus, O., Saleiro, A., Fernandes, A.E., Marinheiro, J., Tomás, C. and Mateus, S. 2021. A new plesiosaur from the Lower Jurassic of Portugal and the early radiation of Plesiosauroidea. Acta Palaeontologica Polonica 66 (2): 369–388. A new plesiosaur partial skeleton, comprising most of the trunk and including axial, limb, and girdle bones, was collected in the lower Sinemurian (Coimbra Formation) of Praia da Concha, near São Pedro de Moel in central west Portugal. The specimen represents a new genus and species, Plesiopharos moelensis gen. et sp. nov. Phylogenetic analysis places this taxon at the base of Plesiosauroidea. Its position is based on this exclusive combination of characters: presence of a straight preaxial margin of the radius; transverse processes of mid-dorsal vertebrae horizontally oriented; ilium with sub-circular cross section of the shaft and subequal anteroposterior expansion of the dorsal blade; straight proximal end of the humerus; and ventral surface of the humerus with an anteroposteriorly long shallow groove between the epipodial facets. In addition, the new taxon has the following autapomorphies: iliac blade with less expanded, rounded and convex anterior flank; highly developed ischial facet of the ilium; apex of the neural spine of the first pectoral vertebra inclined posterodorsally with a small rounded tip. This taxon represents the most complete and the oldest plesiosaur species in the Iberian Peninsula. -
Cretaceous - Tertiary Mass Extinction Meteoritic Versus Volcanic Causes
GENERAL I ARTICLE Cretaceous - Tertiary Mass Extinction Meteoritic Versus Volcanic Causes P V Sukumaran The bolide impact theory for mass extinctions at the Cretaceous-tertiary (K-T) boundary was a revolutionary concept. This theory was contested by short duration global volcanism as a possible alternative cause for the K-T extinction. Though there is a converging evidence for an extra-terrestrial impact coinciding with the P V Sukumaran took his terminal Cretaceous, the causative link between the M Tech degree in impact and the K-T mass extinction is debatable. Thus, Applied Geology from the while the impact theory is re-emerging, available evidence University of Saugar and has been with the is still insufficient to rule out either of the two hypotheses. Geological Survey of India since 1974. His interests Introduction include geochemistry, petrology and palae oceanography. He is It is now widely believed that life on earth began very early in presently posted to the its geological history, probably about 4000 My (million years) Marine Wing of the ago (Mojzsis and others, 1996). Since then it underwent Department and has participated in many several evolutionary branchings to the complex diversity as scientific cruises both as we see today. Nevertheless, it was not a smooth voyage for life Chief Scientist and as a all along, the evolution was punctuated by geologically participating scientist. ins tan taneous events of mass mortality. New species emerged at the expense of their predecessors following each extinction event and life went on evolving ever more vibrantly. In the geologic record of rock strata, such mass extinction events are identifiable based on sudden absence and reduction in diversity of fossil assemblage across stratigraphic boundaries. -
Ichthyodectiform Fishes from the Late Cretaceous
Mesozoic Fishes 5 – Global Diversity and Evolution, G. Arratia, H.-P. Schultze & M. V. H. Wilson (eds.): pp. 247-266, 12 figs., 2 tabs. © 2013 by Verlag Dr. Friedrich Pfeil, München, Germany – ISBN 978-3-89937-159-8 Ichthyodectiform fi shes from the Late Cretaceous (Campanian) of Arkansas, USA Kelly J. IRWIN and Christopher FIELITZ Abstract Several specimens of the ichthyodectiform fishes Xiphactinus audax and Saurocephalus cf. S. lanciformis are reported from the Upper Cretaceous (Campanian) Brownstown Marl and Ozan formations of southwestern Arkansas, U.S.A. Seven individuals of Xiphactinus, based on incomplete specimens, are represented by various elements: disarticu- lated skull bones, jaw fragments, pectoral fin-rays, or vertebrae. The circular vertebral centra are diagnostic for X. audax rather than X. vetus. The specimen of Saurocephalus consists of a three-dimensional skull, lacking much of the skull roof bones. It is identified as Saurocephalus based on the shape of the predentary bone. This specimen provides the first record of entopterygoid teeth in Saurocephalus. These specimens represent new geographic and geologic distribution records of these taxa from the western Gulf Coastal Plain, which biogeographically links records from the eastern Gulf Coastal Plain with those from the Western Interior Sea. Introduction LEIDY (1854) was the first to report the presence of Cretaceous marine vertebrate fossils from Arkansas, yet in the intervening 150+ years, the body of work on the paleoichthyofauna of Arkansas remains limited (WILSON & BRUNER 2004). BARDACK (1965), GOODY (1976), CASE (1978), and RUSSELL (1988) re- ported geographic and geologic distributions for specific taxa, but few descriptive works on fossil fishes are available (see HUSSAKOF 1947; MEYER 1974; BECKER et al. -
Tylosaurus and Pteranodon
Tylosaurus and Pteranodon Estimate size and measure to check estimate. OBJECTIVES Students will: 1. identify the Tylosaurus and Pteranodon as the two state fossils of Kansas, and 2. estimate and check the wingspan of the Pteranodon or the length of the Tylosaurus. MATERIALS FROM THE TRUNK Tylosaurus model Pteranodon model Fossil sample OTHER MATERIALS Ruler or tape measure Masking tape, post-its or something similar to mark measurements on floor TEACHER PREPARATION Decide which of the two fossils you will measure: Pteranodon had a 25-foot wingspan or the Tylosaurus was 49 feet long. Identify a location with 50 linear feet of space that can be used to measure the wingspan of the Pteranodon or the length of the Tylosaurus. Consider using a hallway, playground, or gym. Once a location is identified, use a tape measure to mark the beginning and end of a 25-foot linear space and a 49-foot linear space. This is where the students will measure the two state fossils. HISTORICAL BACKGROUND In 2014 the Kansas Legislature passed a bill making the Tylosaurus and the Pteranodon the state fossils of Kansas. Both of these reptiles lived at the time of dinosaurs, but neither are dinosaurs. Mike Everhart, adjunct curator of paleontology at the Sternberg Museum, geologist Alan Deitrich, and Steven Fisher, a 4-H geology project member, testified in support of the bill. Fossil hunters and natural history museums initiated the adoption of these state fossils. Kansas 4-H geology project members supported the bill. Pteranodon (teh-RAN-oh-don) – “Pteranodon, a great, winged pterosaur with a wingspread of more than 24 feet, which flew the skies of Kansas during the cretaceous period of the mesozoic era, is hereby designated as the official flying fossil of the state Kansas Symbols Traveling Resource Trunk KANSAS HISTORICAL SOCIETY www.kshs.org ©2014 61 of Kansas.” (House Bill 2595) The first Pteranodon specimens discovered in North America were found in western Kansas in 1870 by Othniel Charles Marsh.