Vertebrata: Placodermi) from the Famennian of Belgium
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
FISHING for DUNKLEOSTEUS You’Re Definitely Gonna Need a Bigger Boat by Mark Peter
OOhhiioo GGeeoollooggyy EEXXTTRRAA July 31, 2019 FISHING FOR DUNKLEOSTEUS You’re definitely gonna need a bigger boat by Mark Peter At an estimated maximum length of 6 to 8.8 meters (20–29 sediments that eroded from the Acadian Mountains, combined feet), Dunkleosteus terrelli (Fig. 1) would have been a match for with abundant organic matter from newly evolved land plants even the Hollywood-sized great white shark from the and marine plankton, settled in the basin as dark organic movie Jaws. Surfers, scuba divers, and swimmers can relax, muds. Over millions of years, accumulation of additional however, because Dunkleosteus has been extinct for nearly 360 overlying sediments compacted the muds into black shale rock. million years. Dunkleosteus was a placoderm, a type of armored The rocks that formed from the Late Devonian seafloor fish, that lived during the Late Devonian Period from about sediments (along with fossils of Dunkleosteus) arrived at their 375–359 million years ago. Fossil remains of the large present location of 41 degrees north latitude after several species Dunkleosteus terrelli are present in the Cleveland hundred million years of slow plate tectonic movement as the Member of the Ohio Shale, which contains rocks that are North American Plate moved northward. approximately 360–359 million years old. Figure 1. A reconstruction of a fully-grown Dunkleosteus terrelli, assuming a length of 29 feet, with angler for scale. Modified from illustration by Hugo Salais of Metazoa Studio. Dunkleosteus cruised Late Devonian seas and oceans as an Figure 2. Paleogeographic reconstruction of eastern North America during apex predator, much like the great white shark of today. -
Class Myxini Order Myxiniformes Family Myxinidae (Hagfishes)
Class Myxini Order Myxiniformes Family Myxinidae (hagfishes) • Lacks jaws • Mouth not disk-like • barbels present • Unpaired fins as continuous fin-fold • Branchial skeleton not well developed • Eyes degenerate • 70-200 slime glands • Isoosmotic, simple kidneys, stenohayline, marine • Four rudimentary hearts • No true stomach • Unpaired gonads Class Petromyzontida Order Petromyzontiformes Family Petromyzontidae Class Myxini Order Myxiniformes Family Myxinidae (hagfishes) (Northern Lampreys) • Knot-tying behavior • 8 genera, 34 species • Scavengers • Dorsal fins continuous in • Rely heavily on cutaneous respiration adults • Global, deep sea distribution • Oral disc • Commercial interest – eelskin • 7 pairs of gill openings • Single nostril • Pineal body opening • No bone • No scales • No paired fins • No jaws 1 Class Petromyzontida Order Petromyzontiformes Family Petromyzontidae Class Petromyzontida Order Petromyzontiformes Family Petromyzontidae (Northern Lampreys) (Northern Lampreys) • Anadramous and freshwater • Ammocoete • Parasitic forms: – Non-parasitic forms often • Non-parasitic: freshwater – Parasitic forms often anadramous • Life history Class Conodonta, Conodonts Class Pteraspidiomorphi • Extinct, late Triassic • Extinct • First “teeth” • One of the earliest known vertebrates • No jaws • Dermal skeleton • Cranium and teeth • No jaws • Small, thought to be of paedomorphic origin • Little known, an extinct monophyletic lineage. 2 Class Anapsid Class Cephalaspidomorphi, osteostraci • Extinct, Silurian period • Extinct, early Silurian -
Wales Regional Geology RWM | Wales Regional Geology
Wales regional geology RWM | Wales Regional Geology Contents 1 Introduction Subregions Wales: summary of the regional geology Available information for this region 2 Rock type Younger sedimentary rocks Older sedimentary rocks 3 Basement rocks Rock structure 4 Groundwater 5 Resources 6 Natural processes Further information 7 - 21 Figures 22 - 24 Glossary Clicking on words in green, such as sedimentary or lava will take the reader to a brief non-technical explanation of that word in the Glossary section. By clicking on the highlighted word in the Glossary, the reader will be taken back to the page they were on. Clicking on words in blue, such as Higher Strength Rock or groundwater will take the reader to a brief talking head video or animation providing a non-technical explanation. For the purposes of this work the BGS only used data which was publicly available at the end of February 2016. The one exception to this was the extent of Oil and Gas Authority licensing which was updated to include data to the end of June 2018. 1 RWM | Wales Regional Geology Introduction This region comprises Wales and includes the adjacent inshore area which extends to 20km from the coast. Subregions To present the conclusions of our work in a concise and accessible way, we have divided Wales into 6 subregions (see Figure 1 below). We have selected subregions with broadly similar geological attributes relevant to the safety of a GDF, although there is still considerable variability in each subregion. The boundaries between subregions may locally coincide with the extent of a particular Rock Type of Interest, or may correspond to discrete features such as faults. -
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 -
Categorical Versus Geometric Morphometric Approaches To
[Palaeontology, 2020, pp. 1–16] CATEGORICAL VERSUS GEOMETRIC MORPHOMETRIC APPROACHES TO CHARACTERIZING THE EVOLUTION OF MORPHOLOGICAL DISPARITY IN OSTEOSTRACI (VERTEBRATA, STEM GNATHOSTOMATA) by HUMBERTO G. FERRON 1,2* , JENNY M. GREENWOOD1, BRADLEY DELINE3,CARLOSMARTINEZ-PEREZ 1,2,HECTOR BOTELLA2, ROBERT S. SANSOM4,MARCELLORUTA5 and PHILIP C. J. DONOGHUE1,* 1School of Earth Sciences, University of Bristol, Life Sciences Building, Tyndall Avenue, Bristol, BS8 1TQ, UK; [email protected], [email protected], [email protected] 2Institut Cavanilles de Biodiversitat i Biologia Evolutiva, Universitat de Valencia, C/ Catedratic Jose Beltran Martınez 2, 46980, Paterna, Valencia, Spain; [email protected], [email protected] 3Department of Geosciences, University of West Georgia, Carrollton, GA 30118, USA; [email protected] 4School of Earth & Environmental Sciences, University of Manchester, Manchester, M13 9PT, UK; [email protected] 5School of Life Sciences, University of Lincoln, Riseholme Hall, Lincoln, LN2 2LG, UK; [email protected] *Corresponding authors Typescript received 2 October 2019; accepted in revised form 27 February 2020 Abstract: Morphological variation (disparity) is almost aspects of morphology. Phylomorphospaces reveal conver- invariably characterized by two non-mutually exclusive gence towards a generalized ‘horseshoe’-shaped cranial mor- approaches: (1) quantitatively, through geometric morpho- phology and two strong trends involving major groups of metrics; -
Upper Devonian) of Latvia
Estonian Journal of Earth Sciences, 2021, 70, 1, 3–17 https://doi.org/10.3176/earth.2021.01 Revision of asterolepidoid antiarch remains from the Ogre Formation (Upper Devonian) of Latvia Ervīns Lukševičs Department of Geology, University of Latvia, Raiņa Boulevard 19, Riga LV1586, Latvia; [email protected] Received 3 June 2020, accepted 8 September 2020, available online 15 December 2020 Abstract. The Frasnian (Upper Devonian) antiarch Walterilepis speciosa was first described in 1933 (as Taeniolepis) on the basis of a single specimen. The newly collected material has allowed the head to be described in a more detail, especially the nuchal and paranuchal plates. Other newly described elements include bones of the pectoral appendages and trunk armour, demonstrating a rather high and short trunk armour. The shape and proportions of the head and trunk armour suggest the attribution of Walterilepis to the family Pterichthyodidae; it is most probably closely related to Lepadolepis from the Late Frasnian of Germany. Whilst W. speciosa is endemic to the Latvian part of the Baltic Devonian Basin, the connection to the Rheinisches Schiefergebirge is probably closer than previously presumed. Walterilepis fits into the biostratigraphical column at the same level as Bothriolepis maxima and B. evaldi, indicating the high diversity of antiarchs during Pamūšis time. Key words: Frasnian, biostratigraphy, morphology, placoderm, Baltic Devonian basin. INTRODUCTION noted that the generic name of Gross (1932, 1933a) is preoccupied by the sarcopterygian name Taeniolepis The wellknown Baltic German palaeontologist Walter Trautschold, 1874, and he erected the replacement name Gross, who was born in the close vicinity of Riga, made Walterilepis (Moloshnikov 2001). -
'Placoderm' (Arthrodira)
Jobbins et al. Swiss J Palaeontol (2021) 140:2 https://doi.org/10.1186/s13358-020-00212-w Swiss Journal of Palaeontology RESEARCH ARTICLE Open Access A large Middle Devonian eubrachythoracid ‘placoderm’ (Arthrodira) jaw from northern Gondwana Melina Jobbins1* , Martin Rücklin2, Thodoris Argyriou3 and Christian Klug1 Abstract For the understanding of the evolution of jawed vertebrates and jaws and teeth, ‘placoderms’ are crucial as they exhibit an impressive morphological disparity associated with the early stages of this process. The Devonian of Morocco is famous for its rich occurrences of arthrodire ‘placoderms’. While Late Devonian strata are rich in arthrodire remains, they are less common in older strata. Here, we describe a large tooth-bearing jaw element of Leptodontich- thys ziregensis gen. et sp. nov., an eubrachythoracid arthrodire from the Middle Devonian of Morocco. This species is based on a large posterior superognathal with a strong dentition. The jawbone displays features considered syna- pomorphies of Late Devonian eubrachythoracid arthrodires, with one posterior and one lateral row of conical teeth oriented postero-lingually. μCT-images reveal internal structures including pulp cavities and dentinous tissues. The posterior orientation of the teeth and the traces of a putative occlusal contact on the lingual side of the bone imply that these teeth were hardly used for feeding. Similar to Compagopiscis and Plourdosteus, functional teeth were pos- sibly present during an earlier developmental stage and have been worn entirely. The morphological features of the jaw element suggest a close relationship with plourdosteids. Its size implies that the animal was rather large. Keywords: Arthrodira, Dentition, Food web, Givetian, Maïder basin, Palaeoecology Introduction important to reconstruct character evolution in early ‘Placoderms’ are considered as a paraphyletic grade vertebrates. -
Arthrodira, Homostiidae) from the Emsian of Aragón, Spain, and Its Distribution
FISH FROM THE EMSIAN OF ARAGÓN 139 Tityosteus, A MARINE FISH (ARTHRODIRA, HOMOSTIIDAE) FROM THE EMSIAN OF ARAGÓN, SPAIN, AND ITS DISTRIBUTION Elga MARK-KURIK1 and Peter CARLS2 1 Institute of Geology. Tallinn University of Technology, Estonia Avenue 7, 10143 Tallinn, Estonia. E-mail: [email protected] 2 Institut für Umweltgeologie, Technische Universität, Braunschweig, Pockels- Str. 3, D 38106, Germany. Mark-Kurik, E. and Carls, P. 2004. Tityosteus, a marine fish (Arthrodira, Homostiidae) from the Emsian of Aragón, Spain, and its distribution. [Tityosteus, un pez marino (Arthrodira, Homostiidae) del Emsiense de Aragón, España, y su distribución.] Revista Española de Paleontología, 19 (2), 139-144. ISSN 0213-6937. ABSTRACT A right marginal plate (over 11 cm long) of Tityosteus cf. rieversae Gross, 1960, emend., has been found in the late part of the Early Emsian (late Zlichovian) in the Mariposas Fm. of the Eastern Iberian Cordillera in south- ern Aragón. The palaeoecological conditions correspond to a hemipelagic ensialic basin, with predominant ele- ments of Hercynic biofacies but still with photic bottom. The Emsian genus Tityosteus is now known from the Hunsrück Schiefer of Germany and the closely connected Ibero-Armorican Trough and also from the more dis- tant Minusinsk Basin of southern Siberia. Palaeo-oceans between western Europe and southern Siberia were no zoogeographical barriers for these large, possibly microphagous fishes in open sea. The name of the type spe- cies of Tityosteus is emended. Keywords: Placodermi, marginal plate, palaeoecology, palaeozoogeography, late Zlichovian. RESUMEN Se describe una placa marginal derecha (más de 11 cm de longitud) de Tityosteus cf. rieversae Gross, 1960, emend., de la parte tardía del Emsiense Inferior (Zlichoviense tardío) de la Fm. -
THE CLASSIFICATION and EVOLUTION of the HETEROSTRACI Since 1858, When Huxley Demonstrated That in the Histological Struc
ACTA PALAEONT OLOGICA POLONICA Vol. VII 1 9 6 2 N os. 1-2 L. BEVERLY TARLO THE CLASSIFICATION AND EVOLUTION OF THE HETEROSTRACI Abstract. - An outline classification is given of the Hetero straci, with diagnoses . of th e following orders and suborders: Astraspidiformes, Eriptychiiformes, Cya thaspidiformes (Cyathaspidida, Poraspidida, Ctenaspidida), Psammosteiformes (Tes seraspidida, Psarnmosteida) , Traquairaspidiformes, Pteraspidiformes (Pte ras pidida, Doryaspidida), Cardipeltiformes and Amphiaspidiformes (Amphiaspidida, Hiber naspidida, Eglonaspidida). It is show n that the various orders fall into four m ain evolutionary lineages ~ cyathaspid, psammosteid, pteraspid and amphiaspid, and these are traced from primitive te ssellated forms. A tentative phylogeny is pro posed and alternatives are discussed. INTRODUCTION Since 1858, when Huxley demonstrated that in the histological struc ture of their dermal bone Cephalaspis and Pteraspis were quite different from one another, it has been recognized that there were two distinct groups of ostracoderms for which Lankester (1868-70) proposed the names Osteostraci and Heterostraci respectively. Although these groups are generally considered to be related to on e another, Lankester belie ved that "the Heterostraci are at present associated with the Osteostraci because they are found in the same beds, because they have, like Cepha laspis, a large head shield, and because there is nothing else with which to associate them". In 1889, Cop e united these two groups in the Ostracodermi which, together with the modern cyclostomes, he placed in the Class Agnatha, and although this proposal was at first opposed by Traquair (1899) and Woodward (1891b), subsequent work has shown that it was correct as both the Osteostraci and the Heterostraci were agnathous. -
Contributions in BIOLOGY and GEOLOGY
MILWAUKEE PUBLIC MUSEUM Contributions In BIOLOGY and GEOLOGY Number 51 November 29, 1982 A Compendium of Fossil Marine Families J. John Sepkoski, Jr. MILWAUKEE PUBLIC MUSEUM Contributions in BIOLOGY and GEOLOGY Number 51 November 29, 1982 A COMPENDIUM OF FOSSIL MARINE FAMILIES J. JOHN SEPKOSKI, JR. Department of the Geophysical Sciences University of Chicago REVIEWERS FOR THIS PUBLICATION: Robert Gernant, University of Wisconsin-Milwaukee David M. Raup, Field Museum of Natural History Frederick R. Schram, San Diego Natural History Museum Peter M. Sheehan, Milwaukee Public Museum ISBN 0-893260-081-9 Milwaukee Public Museum Press Published by the Order of the Board of Trustees CONTENTS Abstract ---- ---------- -- - ----------------------- 2 Introduction -- --- -- ------ - - - ------- - ----------- - - - 2 Compendium ----------------------------- -- ------ 6 Protozoa ----- - ------- - - - -- -- - -------- - ------ - 6 Porifera------------- --- ---------------------- 9 Archaeocyatha -- - ------ - ------ - - -- ---------- - - - - 14 Coelenterata -- - -- --- -- - - -- - - - - -- - -- - -- - - -- -- - -- 17 Platyhelminthes - - -- - - - -- - - -- - -- - -- - -- -- --- - - - - - - 24 Rhynchocoela - ---- - - - - ---- --- ---- - - ----------- - 24 Priapulida ------ ---- - - - - -- - - -- - ------ - -- ------ 24 Nematoda - -- - --- --- -- - -- --- - -- --- ---- -- - - -- -- 24 Mollusca ------------- --- --------------- ------ 24 Sipunculida ---------- --- ------------ ---- -- --- - 46 Echiurida ------ - --- - - - - - --- --- - -- --- - -- - - --- -
Fishes Scales & Tails Scale Types 1
Phylum Chordata SUBPHYLUM VERTEBRATA Metameric chordates Linear series of cartilaginous or boney support (vertebrae) surrounding or replacing the notochord Expanded anterior portion of nervous system THE FISHES SCALES & TAILS SCALE TYPES 1. COSMOID (most primitive) First found on ostracaderm agnathans, thick & boney - composed of: Ganoine (enamel outer layer) Cosmine (thick under layer) Spongy bone Lamellar bone Perhaps selected for protection against eurypterids, but decreased flexibility 2. GANOID (primitive, still found on some living fish like gar) 3. PLACOID (old scale type found on the chondrichthyes) Dentine, tooth-like 4. CYCLOID (more recent scale type, found in modern osteichthyes) 5. CTENOID (most modern scale type, found in modern osteichthyes) TAILS HETEROCERCAL (primitive, still found on chondrichthyes) ABBREVIATED HETEROCERCAL (found on some primitive living fish like gar) DIPHYCERCAL (primitive, found on sarcopterygii) HOMOCERCAL (most modern, found on most modern osteichthyes) Agnatha (class) [connect the taxa] Cyclostomata (order) Placodermi Acanthodii (class) (class) Chondrichthyes (class) Osteichthyes (class) Actinopterygii (subclass) Sarcopterygii (subclass) Dipnoi (order) Crossopterygii (order) Ripidistia (suborder) Coelacanthiformes (suborder) Chondrostei (infra class) Holostei (infra class) Teleostei (infra class) CLASS AGNATHA ("without jaws") Most primitive - first fossils in Ordovician Bottom feeders, dorsal/ventral flattened Cosmoid scales (Ostracoderms) Pair of eyes + pineal eye - present in a few living fish and reptiles - regulates circadian rhythms Nine - seven gill pouches No paired appendages, medial nosril ORDER CYCLOSTOMATA (60 spp) Last living representatives - lampreys & hagfish Notochord not replaced by vertebrae Cartilaginous cranium, scaleless body Sea lamprey predaceous - horny teeth in buccal cavity & on tongue - secretes anti-coaggulant Lateral Line System No stomach or spleen 5 - 7 year life span - adults move into freshwater streams, spawn, & die. -
Durham Research Online
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Durham Research Online Durham Research Online Deposited in DRO: 20 February 2018 Version of attached le: Published Version Peer-review status of attached le: Peer-reviewed Citation for published item: Rossetter, Thomas (2018) 'Realism on the rocks : novel success and James Hutton's theory of the earth.', Studies in history and philosophy of science part A., 67 . pp. 1-13. Further information on publisher's website: https://doi.org/10.1016/j.shpsa.2017.10.005 Publisher's copyright statement: c 2017 The Author. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). Additional information: Use policy The full-text may be used and/or reproduced, and given to third parties in any format or medium, without prior permission or charge, for personal research or study, educational, or not-for-prot purposes provided that: • a full bibliographic reference is made to the original source • a link is made to the metadata record in DRO • the full-text is not changed in any way The full-text must not be sold in any format or medium without the formal permission of the copyright holders. Please consult the full DRO policy for further details. Durham University Library, Stockton Road, Durham DH1 3LY, United Kingdom Tel : +44 (0)191 334 3042 | Fax : +44 (0)191 334 2971 http://dro.dur.ac.uk Studies in History and Philosophy of Science 67 (2018) 1e13 Contents lists available at ScienceDirect Studies in History and Philosophy of Science journal homepage: www.elsevier.com/locate/shpsa Realism on the rocks: Novel success and James Hutton’s theory of the earth Thomas Rossetter Department of Philosophy, Durham University, 50 Old Elvet, Durham, DH1 3HN, United Kingdom article info abstract Article history: In this paper, I introduce a new historical case study into the scientific realism debate.