Note on Pterygotus Anglicus Agassiz (Eurypterida: Devonian) from the Campbellton Formation, New Brunswick Randall F
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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; -
Geological Survey of Ohio
GEOLOGICAL SURVEY OF OHIO. VOL. I.—PART II. PALÆONTOLOGY. SECTION II. DESCRIPTIONS OF FOSSIL FISHES. BY J. S. NEWBERRY. Digital version copyrighted ©2012 by Don Chesnut. THE CLASSIFICATION AND GEOLOGICAL DISTRIBUTION OF OUR FOSSIL FISHES. So little is generally known in regard to American fossil fishes, that I have thought the notes which I now give upon some of them would be more interesting and intelligible if those into whose hands they will fall could have a more comprehensive view of this branch of palæontology than they afford. I shall therefore preface the descriptions which follow with a few words on the geological distribution of our Palæozoic fishes, and on the relations which they sustain to fossil forms found in other countries, and to living fishes. This seems the more necessary, as no summary of what is known of our fossil fishes has ever been given, and the literature of the subject is so scattered through scientific journals and the proceedings of learned societies, as to be practically inaccessible to most of those who will be readers of this report. I. THE ZOOLOGICAL RELATIONS OF OUR FOSSIL FISHES. To the common observer, the class of Fishes seems to be well defined and quite distin ct from all the other groups o f vertebrate animals; but the comparative anatomist finds in certain unusual and aberrant forms peculiarities of structure which link the Fishes to the Invertebrates below and Amphibians above, in such a way as to render it difficult, if not impossible, to draw the lines sharply between these great groups. -
Chelicerata; Eurypterida) from the Campbellton Formation, New Brunswick, Canada Randall F
Document generated on 10/01/2021 9:05 a.m. Atlantic Geology Nineteenth century collections of Pterygotus anglicus Agassiz (Chelicerata; Eurypterida) from the Campbellton Formation, New Brunswick, Canada Randall F. Miller Volume 43, 2007 Article abstract The Devonian fauna from the Campbellton Formation of northern New URI: https://id.erudit.org/iderudit/ageo43art12 Brunswick was discovered in 1881 at the classic locality in Campbellton. About a decade later A.S. Woodward at the British Museum (Natural History) (now See table of contents the Natural History Museum, London) acquired specimens through fossil dealer R.F. Damon. Woodward was among the first to describe the fish assemblage of ostracoderms, arthrodires, acanthodians and chondrichthyans. Publisher(s) At the same time the museum also acquired specimens of a large pterygotid eurypterid. Although the vertebrates received considerable attention, the Atlantic Geoscience Society pterygotids at the Natural History Museum, London are described here for the first time. The first pterygotid specimens collected in 1881 by the Geological ISSN Survey of Canada were later identified by Clarke and Ruedemann in 1912 as Pterygotus atlanticus, although they suggested it might be a variant of 0843-5561 (print) Pterygotus anglicus Agassiz. An almost complete pterygotid recovered in 1994 1718-7885 (digital) from the Campbellton Formation at a new locality in Atholville, less than two kilometres west of Campbellton, has been identified as P. anglicus Agassiz. Like Explore this journal the specimens described by Clarke and Ruedemann, the material from the Natural History Museum, London is herein referred to P. anglicus. Cite this article Miller, R. F. (2007). Nineteenth century collections of Pterygotus anglicus Agassiz (Chelicerata; Eurypterida) from the Campbellton Formation, New Brunswick, Canada. -
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. -
Designing the Dinosaur: Richard Owen's Response to Robert Edmond Grant Author(S): Adrian J
Designing the Dinosaur: Richard Owen's Response to Robert Edmond Grant Author(s): Adrian J. Desmond Source: Isis, Vol. 70, No. 2 (Jun., 1979), pp. 224-234 Published by: The University of Chicago Press on behalf of The History of Science Society Stable URL: http://www.jstor.org/stable/230789 . Accessed: 16/10/2013 13:00 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. The University of Chicago Press and The History of Science Society are collaborating with JSTOR to digitize, preserve and extend access to Isis. http://www.jstor.org This content downloaded from 150.135.115.18 on Wed, 16 Oct 2013 13:00:27 PM All use subject to JSTOR Terms and Conditions Designing the Dinosaur: Richard Owen's Response to Robert Edmond Grant By Adrian J. Desmond* I N THEIR PAPER on "The Earliest Discoveries of Dinosaurs" Justin Delair and William Sarjeant permit Richard Owen to step in at the last moment and cap two decades of frenzied fossil collecting with the word "dinosaur."' This approach, I believe, denies Owen's real achievement while leaving a less than fair impression of the creative aspect of science. -
A Sea Scorpion Claw from the Lower Devonian of China (Chelicerata: Eurypterida) Bo Wang & Zhikun Gai Published Online: 13 Jan 2014
This article was downloaded by: [Institute of Vertebrate Paleontology and Paleoanthropology] On: 10 February 2014, At: 19:32 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Alcheringa: An Australasian Journal of Palaeontology Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/talc20 A sea scorpion claw from the Lower Devonian of China (Chelicerata: Eurypterida) Bo Wang & Zhikun Gai Published online: 13 Jan 2014. To cite this article: Bo Wang & Zhikun Gai , Alcheringa: An Australasian Journal of Palaeontology (2014): A sea scorpion claw from the Lower Devonian of China (Chelicerata: Eurypterida), Alcheringa: An Australasian Journal of Palaeontology, DOI: 10.1080/03115518.2014.870819 To link to this article: http://dx.doi.org/10.1080/03115518.2014.870819 PLEASE SCROLL DOWN FOR ARTICLE Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content. Any opinions and views expressed in this publication are the opinions and views of the authors, and are not the views of or endorsed by Taylor & Francis. The accuracy of the Content should not be relied upon and should be independently verified with primary sources of information. Taylor and Francis shall not be liable for any losses, actions, claims, proceedings, demands, costs, expenses, damages, and other liabilities whatsoever or howsoever caused arising directly or indirectly in connection with, in relation to or arising out of the use of the Content. -
Tayside, Central and Fife Tayside, Central and Fife
Detail of the Lower Devonian jawless, armoured fish Cephalaspis from Balruddery Den. © Perth Museum & Art Gallery, Perth & Kinross Council Review of Fossil Collections in Scotland Tayside, Central and Fife Tayside, Central and Fife Stirling Smith Art Gallery and Museum Perth Museum and Art Gallery (Culture Perth and Kinross) The McManus: Dundee’s Art Gallery and Museum (Leisure and Culture Dundee) Broughty Castle (Leisure and Culture Dundee) D’Arcy Thompson Zoology Museum and University Herbarium (University of Dundee Museum Collections) Montrose Museum (Angus Alive) Museums of the University of St Andrews Fife Collections Centre (Fife Cultural Trust) St Andrews Museum (Fife Cultural Trust) Kirkcaldy Galleries (Fife Cultural Trust) Falkirk Collections Centre (Falkirk Community Trust) 1 Stirling Smith Art Gallery and Museum Collection type: Independent Accreditation: 2016 Dumbarton Road, Stirling, FK8 2KR Contact: [email protected] Location of collections The Smith Art Gallery and Museum, formerly known as the Smith Institute, was established at the bequest of artist Thomas Stuart Smith (1815-1869) on land supplied by the Burgh of Stirling. The Institute opened in 1874. Fossils are housed onsite in one of several storerooms. Size of collections 700 fossils. Onsite records The CMS has recently been updated to Adlib (Axiel Collection); all fossils have a basic entry with additional details on MDA cards. Collection highlights 1. Fossils linked to Robert Kidston (1852-1924). 2. Silurian graptolite fossils linked to Professor Henry Alleyne Nicholson (1844-1899). 3. Dura Den fossils linked to Reverend John Anderson (1796-1864). Published information Traquair, R.H. (1900). XXXII.—Report on Fossil Fishes collected by the Geological Survey of Scotland in the Silurian Rocks of the South of Scotland. -
Categorical Versus Geometric Morphometric Approaches to Characterising the Evolution of Morphological Disparity in Osteostraci (Vertebrata, Stem-Gnathostomata)
Palaeontology CATEGORICAL VERSUS GEOMETRIC MORPHOMETRIC APPROACHES TO CHARACTERISING THE EVOLUTION OF MORPHOLOGICAL DISPARITY IN OSTEOSTRACI (VERTEBRATA, STEM-GNATHOSTOMATA) Journal: Palaeontology Manuscript ID PALA-10-19-4616-OA Manuscript Type: Original Article Date Submitted by the 02-Oct-2019 Author: Complete List of Authors: Ferrón, Humberto; Universitat de Valencia Institut Cavanilles de Biodiversitat i Biologia Evolutiva, Greenwood, Jenny; University of Bristol School of Earth Sciences Deline, Bradley; University of West Georgia, Geosciences Martínez Pérez, Carlos; Universitat de Valencia Institut Cavanilles de Biodiversitat i Biologia Evolutiva, ; University of Bristol School of Biological Sciences, BOTELLA, HECTOR; university of Valencia, geology Sansom, Robert; University of Manchester, School of Earth and Environmental Sciences Ruta, Marcello; University of Lincoln, Life Sciences; Donoghue, Philip; University of Bristo, School of Earth Sciences Key words: Disparity, Osteostraci, Geometric morphometrics, Categorical data Note: The following files were submitted by the author for peer review, but cannot be converted to PDF. You must view these files (e.g. movies) online. File S1.rar Palaeontology Page 1 of 32 Palaeontology 1 2 3 CATEGORICAL VERSUS GEOMETRIC MORPHOMETRIC APPROACHES TO CHARACTERISING THE EVOLUTION 4 5 OF MORPHOLOGICAL DISPARITY IN OSTEOSTRACI (VERTEBRATA, STEM-GNATHOSTOMATA) 6 7 8 by HUMBERTO G. FERRÓN1,2*, JENNY M. GREENWOOD1, BRADLEY DELINE3, CARLOS MARTÍNEZ-PÉREZ1,2, 9 10 HÉCTOR BOTELLA2, ROBERT S. SANSOM4, -
Description of a New Osteostracan Species from Ukraine with a Brief Analysis of the Interrelationships of Scolenaspida
Description of a new osteostracan species from Ukraine with a brief analysis of the interrelationships of Scolenaspida Anders Carlsson Degree project in biology, 2006 Examensarbete i biologi 20p, 2006 Institutionen för fysiologi och utvecklingsbiologi, Avdelningen för evolutionär organismbiologi Supervisor: Henning Blom Sammanfattning Under devonperioden (ca. 400-350 miljoner år sedan) levde många märkliga former av ryggradsdjur som inte har några nutida ättlingar. En av dessa grupper var osteostracerna, en form av käklösa fiskar som anses vara de närmaste släktingarna till käkförsedda fiskar. De bestod av en hästskoformad huvudsköld av ben, ofta försedd med bakåtböjda horn, och en fiskliknande bakkropp, täckt av ledade fjäll. Skölden hade ögon och en enda näsöppning på ovansidan, och munnen och flera par gälöppningar på undersidan . I mitt examensarbete beskrivs ett nytt släkte och art av osteostracerna, Voichyschynaspis longicornualis gen. et sp. nov. Beskrivningen är baserad på fossilt material hittat i Dniestrdalen i Ukraina. Detta nya släkte har likheter med släktena Zychaspis och Stensiopelta. För att testa det nya släktets plats i släktträdet görs en fylogenetisk analys tillsammans med dess närmaste släktingar, Zychaspis och Stensiopelta. Analysen försöker också reda ut släktskapsförhållandena mellan de båda andra släktenas arter. Voichyschynaspis visar sig vara närmast släkt med Stensiopelta, som visar sig vara monofyletiskt, det vill säga alla dess arter har en gemensam förfader. Zychaspis är mer problematiskt eftersom en av dess arter inte med säkerhet kan föras till det. 1 Description of a new osteostracan species from Ukraine with a brief analysis of the interrelationships of Scolenaspida ANDERS CARLSSON Biology Education Centre and Department of Developmental Biology and Comparative Physiology, Subdepartment of Evolutionary Organism Biology, Uppsala University Supervised by Dr. -
An Isolated Pterygotid Ramus (Chelicerata: Eurypterida) from the Devonian Beartooth Butte Formation, Wyoming
Journal of Paleontology, 84(6), 2010, p. 1206–1208 Copyright ’ 2010, The Paleontological Society 0022-3360/10/0084-1206$03.00 AN ISOLATED PTERYGOTID RAMUS (CHELICERATA: EURYPTERIDA) FROM THE DEVONIAN BEARTOOTH BUTTE FORMATION, WYOMING JAMES C. LAMSDELL1 AND DAVID A. LEGG2 1Paleontological Institute, University of Kansas, 1475 Jayhawk Boulevard, Lawrence, Kansas 66045, USA, ,[email protected].; and 2Department of Earth Science and Engineering, Imperial College, London SW7 2AZ, UK ABSTRACT—An isolated ramus of the pterygotid eurypterid Jaekelopterus cf. howelli from the Early Devonian (Pragian) Beartooth Butte Formation (Cottonwood Canyon, north-western Wyoming) is described. Pterygotid taxonomy and synonymy is briefly discussed with the genera Pterygotus, Acutiramus and Jaekelopterus shown to be potential synonyms. The use of cheliceral denticulation patterns as a generic-level character is discouraged in light of variations within genera and its unsuitability as a major characteristic in the other eurypterid families. INTRODUCTION the type section of the Beartooth Butte Formation in TERYGOTIDS ARE a diverse group of predatory Palaeozoic Beartooth Butte, which is Early Devonian in age. For a more P eurypterids, famed for being amongst the largest arthro- comprehensive discussion of the formation, its stratigraphy pods ever to have lived (Braddy et al., 2008a). The and paleoenvironment, see Tetlie (2007b). Vertebrate biostra- Pterygotidae are characterized by the possession of enlarged tigraphy (Elliot and Ilyes, 1996) indicates that the Cotton- raptorial chelicerae, non-spiniferous appendages III–V, undi- wood Canyon section is Pragian whereas the type section at vided medial appendages, laterally expanded pretelson and a Beartooth Butte is Emsian. Stable oxygen and isotope data broad paddle-like telson with marginal ornamentation (Tetlie (Poulson in Fiorillo, 2000) indicate that the Beartooth Butte and Briggs, 2009). -
GY 112 Lecture Notes D
GY 112 lecture notes D. Haywick (2006) 1 GY 112 Lecture Notes Evolution of the Chordates Lecture Goals: A) The first animals with backbones (conodonts) B) The fish family tree C) Other key chordate evolutionary events Textbook reference: Levin 7th edition (2003) Chapter 10; Levin 8th edition (2006) Chapter 12 A) The conodonts By now you should realize that there are still a lot of mysteries in Earth history. The same can be said about biology, chemistry and physics. Science does not have all the answers, nor will it ever find all the answers. However, every once in a while, a long standing mystery or problem is solved. I bet you're thinking that in order to do this, a clever scientist had to dedicate his or her entire life to finding the solution. He/She had to work non- stop, day and night, taking a break only to eat, sleep for a few hours, and, occasionally, pee. Yep, sometimes this is what's done. Other times, however, it's just blind luck. Such is the case with a formerly mysterious group of animal remains simply classified as the conodonts. These hard body parts (see scanning electron microscope image to the left from, http://earthnet-geonet.ca/earth/ranges_e.php?s=conodonts) are usually quite small (less than 1 mm), are composed of the mineral apatite [Ca5(PO4)3(OH,F)] and really look like tiny teeth. They have been long used for biostratigraphy and there are many well-know examples of conodont index fossils, but apart from the fact that they look like teeth, and that they are now all extinct, no one really knew what they were. -
Phylum Chordata with Its Characters
Classification of phylum Chordata with its characters: TIG The chordates form a large heterogeneous group of members differing widely from one another in many respects. Due to great diversity in chordate forms, different schemes of classification have been proposed by a number of taxonomists from time to time. The classification followed is simplified and is a synthesis of most recent classifications. Table 1.2 gives an outline classification of the phylum Chordata. Phylum Chordata: Widely diversified (differing) in size, habits and habitat, bilaterally symmetrical, metamerically segmented, triploblastic, coelomate deuterostomes. All the chordates possess a supporting skeletal rod or notochord, a hollow dorsal nerve cord and paired gill-slits at some stage of their life history which may persist, change or disappear in adults. Cambrian to Recent. About 50,000 species. Phylum Chordata can be divided into two groups: A. Acrania (Protochordata) and B. Craniata (Euchordata) which show contrasting characters. Group A. Acrania (Protochordata): (Gr., a = absent; kranion = head or Gr., protos = first; chorde = cord). All are marine, small, primitive or lower chordates. No cranium, jaws, vertebral column, paired appendages. About 2,000 species. The Acrania is divided into three subphyla- Hemichordata, Urochordata and Cephalochordata. Subphylum I. Hemichordata: Gr., hemi = half; chorde = cord). Body divided into 3 regions- proboscis, collar and trunk. Notochord doubtful, short confined to proboscis and non-homologous with that of chordates. Class 1. Enteropneusta: (Gr., enteron = gut; pneustos = breathed). Body large and worm-like. Gill-slits numerous and paired. Alimentary canal straight. Acorn or tongue worms. Enteropneusts include 3 families, 15 genera and 70 species. Examples- Balanoglossus, Saccoglossus, Ptychodera.