Superclass: Agnatha
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Classes of Fish #1 Agnatha : Jawless Fish 1) Oldest of All Fish 500 Mya 2) No Jaw 3) Eel-Like Body 4) Light Skeleton Made out of Cartilage
Classes of Fish #1 Agnatha : Jawless Fish 1) Oldest of all fish 500 mya 2) No Jaw 3) Eel-like Body 4) Light skeleton made out of cartilage. 5) Gill slits on the side of the body. 6) Unpaired fins 7) Examples: Lamprey and Hagfish Objectives: 1. List the three classes of fish. Draw a simple picture for each class and provide a one sentence description. 2. Describe the purposes associated with the lateral line http://www.flickr.com/photos/boarderjon/294353224/ system and the swim bladder. #2 Chondrichthyes : Cartilagenous fish 1) Stream-lined Body 2) Jaws Formed from a bony gill arch 3) Skeleton made of cartilage strengthened be calcium carbonate. A thin layer of bone covers the cartilage. 4)Teeth: modified scales 5) Some possess a lateral line system 6) Examples: Sharks, Rays, and Skates 1 #3 Osteichthyes : Bony Fish 1) Skeleton made of bone . 2) Lateral Line System : Specialized sensory system that runs along the length of the fish. It accurately indicates the position and rate of movement of the 2 Groups of Bony Fish fish. In addition, it can also detect motion of other 1) Ray-finned fish : Fins supported by living things in the water. It is similar in function to bony rays. hearing. Example: Perch 3) Gill Cover : A hard plate called an operculum covers 2) Lobe-finned fish : Fin is a fleshy lobe and protects the gills. Muscles attached to the supported by bone. operculum allow it to move in order to push water Example: Lungfish through the gills. Fish that do not have operculum must swim in order to breath. -
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. -
Fish and Amphibians
Fish and Amphibians Geology 331 Paleontology Phylum Chordata: Subphyla Urochordata, Cephalochordata, and: Subphylum Vertebrata Class Agnatha: jawless fish, includes the hagfish, conodonts, lampreys, and ostracoderms (armored jawless fish) Gnathostomates: jawed fish Class Chondrichthyes: cartilaginous fish Class Placoderms: armored fish Class Osteichthyes: bony fish Subclass Actinopterygians: ray-finned fish Subclass Sarcopterygians: lobe-finned fish Order Dipnoans: lung fish Order Crossopterygians: coelocanths and rhipidistians Class Amphibia Urochordates: Sea Squirts. Adults have a pharynx with gill slits. Larval forms are free-swimming and have a notochord. Chordates are thought to have evolved from the larval form by precocious sexual maturation. Chordate evolution Cephalochordate: Branchiostoma, the lancelet Pikaia, a cephalochordate from the Burgess Shale Yunnanozoon, a cephalochordate from the Lower Cambrian of China Haikouichthys, agnathan, Lower Cambrian of China - Chengjiang fauna, scale is 5 mm A living jawless fish, the lamprey, Class Agnatha Jawless fish do have teeth! A fossil jawless fish, Class Agnatha, Ostracoderm, Hemicyclaspis, Silurian Agnathan, Ostracoderm, Athenaegis, Silurian of Canada Agnathan, Ostracoderm, Pteraspis, Devonian of the U.K. Agnathan, Ostracoderm, Liliaspis, Devonian of Russia Jaws evolved by modification of the gill arch bones. The placoderms were the armored fish of the Paleozoic Placoderm, Dunkleosteus, Devonian of Ohio Asterolepis, Placoderms, Devonian of Latvia Placoderm, Devonian of Australia Chondrichthyes: A freshwater shark of the Carboniferous Fossil tooth of a Great White shark Chondrichthyes, Great White Shark Chondrichthyes, Carcharhinus Sphyrna - hammerhead shark Himantura - a ray Manta Ray Fish Anatomy: Ray-finned fish Osteichthyes: ray-finned fish: clownfish Osteichthyes: ray-finned fish, deep water species Lophius, an Eocene fish showing the ray fins. This is an anglerfish. -
Evolutionary Crossroads in Developmental Biology: Cyclostomes (Lamprey and Hagfish) Sebastian M
PRIMER SERIES PRIMER 2091 Development 139, 2091-2099 (2012) doi:10.1242/dev.074716 © 2012. Published by The Company of Biologists Ltd Evolutionary crossroads in developmental biology: cyclostomes (lamprey and hagfish) Sebastian M. Shimeld1,* and Phillip C. J. Donoghue2 Summary and is appealing because it implies a gradual assembly of vertebrate Lampreys and hagfish, which together are known as the characters, and supports the hagfish and lampreys as experimental cyclostomes or ‘agnathans’, are the only surviving lineages of models for distinct craniate and vertebrate evolutionary grades (i.e. jawless fish. They diverged early in vertebrate evolution, perceived ‘stages’ in evolution). However, only comparative before the origin of the hinged jaws that are characteristic of morphology provides support for this phylogenetic hypothesis. The gnathostome (jawed) vertebrates and before the evolution of competing hypothesis, which unites lampreys and hagfish as sister paired appendages. However, they do share numerous taxa in the clade Cyclostomata, thus equally related to characteristics with jawed vertebrates. Studies of cyclostome gnathostomes, has enjoyed unequivocal support from phylogenetic development can thus help us to understand when, and how, analyses of protein-coding sequence data (e.g. Delarbre et al., 2002; key aspects of the vertebrate body evolved. Here, we Furlong and Holland, 2002; Kuraku et al., 1999). Support for summarise the development of cyclostomes, highlighting the cyclostome theory is now overwhelming, with the recognition of key species studied and experimental methods available. We novel families of non-coding microRNAs that are shared then discuss how studies of cyclostomes have provided exclusively by hagfish and lampreys (Heimberg et al., 2010). -
Marine Animals VERTEBRATES
Marine Animals VERTEBRATES OCN 201 Biology Lecture 7 Arthropods Segmented Worms The Animal Chordates Family Tree Molluscs Lophophores Echinoderms Round Worms Cnidarians Bilateria Rotifers Ctenophores Radiata Flatworms Proboscis Sponges Worms Ancestral Protist The Chordates Invertebrates Vertebrates Chordate Features • Presence of a notochord • Dorsal hollow nerve cord • Pharyngeal slits (originally for feeding, later modified) Invertebrate Chordates Tunicates Lancelets • Pelagic or benthic • Small fish-like • Often colonial • Suspension feeder • Suspension feeders • Can swim, but usually stays partly buried Amphioxus The Major Fish Groups • Jawless fishes (Agnatha) • Cartilaginous fishes (Chondrichthyes) • Bony fishes (Osteichthyes) Agnatha Lamprey • No jaws • No appendages • Cartilaginous • Parasites or Scavengers Hagfish Chondrichthyes (Cartilaginous Fish) • Sharks Skates and Rays • Skeleton of cartilage • Have jaws • Carnivores or Planktivores Chondrichthyes: Planktivores • Planktivores (filter feeders) are largest • Gaping mouth with small or no teeth • Gill rakers • Manta Ray (8 m across!) • Whale Shark (up to 17 m long!) Gill Rakers Gill Arch Cookie-Cutter Shark Osteichthyes • 22,000 species • From about 1 cm to 8 m • Surface to deep ≥ 8370 m Smallest, lightest Most Massive bony fish: Mola Mola Stout Infant fish Up to 1300 kg and 3 m tip to tip Feeds on gelatinous zooplankton Examples of feeding strategies Herbivores (algae) Planktivores (Filter Feeders) H2O filter: gill rakers mouth gill opening gut Predators Parrot Fish - eats coral Tuna -
The Morphology and Biomechanics of Jaw Structures in Chondrichthyes
University of Rhode Island DigitalCommons@URI Open Access Master's Theses 2013 THE MORPHOLOGY AND BIOMECHANICS OF JAW STRUCTURES IN CHONDRICHTHYES Jordan Balaban University of Rhode Island, [email protected] Follow this and additional works at: https://digitalcommons.uri.edu/theses Recommended Citation Balaban, Jordan, "THE MORPHOLOGY AND BIOMECHANICS OF JAW STRUCTURES IN CHONDRICHTHYES" (2013). Open Access Master's Theses. Paper 130. https://digitalcommons.uri.edu/theses/130 This Thesis is brought to you for free and open access by DigitalCommons@URI. It has been accepted for inclusion in Open Access Master's Theses by an authorized administrator of DigitalCommons@URI. For more information, please contact [email protected]. THE MORPHOLOGY AND BIOMECHANICS OF JAW STRUCTURES IN CHONDRICHTHYES BY JORDAN BALABAN A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE IN BIOLOGICAL AND ENVIRONMENTAL SCIENCES UNIVERSITY OF RHODE ISLAND 2013 MASTER OF SCIENCE THESIS OF JORDAN BALABAN APPROVED: Thesis Committee: Major Professor____Dr. Cheryl Wilga________________ ____Dr. Adam P. Summers____________ _____Dr. Holly Dunsworth_____________ ____Dr. Nasser H. Zawia______________ DEAN OF THE GRADUATE SCHOOL UNIVERSITY OF RHODE ISLAND 2013 ABSTRACT The skeletons of chondrichthyans (sharks, skates, rays, and chimeras) are composed entirely of cartilage, yet must still provide the skeletal support that bone does in other vertebrates. There is also an incredible range of diversity in the morphology of the cartilaginous skeleton of the feeding apparatus in Chondrichthyans. The goal of this research is to provide insight into the morphological evolution and biomechanical function of the cranial skeleton in chondrichthyans. Feeding style changes can occur with morphological changes in the skeletal elements of the shark feeding apparatus. -
Agnatha, Chondrichthyes and Osteichthyes
See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/311861377 Agnatha, Chondrichthyes and Osteichthyes Chapter · November 2016 CITATIONS READS 0 1,531 2 authors: Antonis Petrou Charitos Zapitis AP Marine Env.Consultancy Ltd & Enalia Physis Environmental Research Centre University of Derby 29 PUBLICATIONS 131 CITATIONS 1 PUBLICATION 0 CITATIONS SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: Lionfish in the Mediterranean View project PCY1 - Investigating the effects of recreational diving on the macroalgal communities of the 'Zenobia' shipwreck (Cyprus) View project All content following this page was uploaded by Charitos Zapitis on 24 December 2016. The user has requested enhancement of the downloaded file. Chapter 26 - Agnatha CHAPTER 26: AGNATHA, CHONDRICHTHYES AND OSTEICHTHYES FISHES Antonis Petrou and Charitos Zapitis 1. INTRODUCTION The classification of fishes is not straightforward since they do not form a natural scientific grouping like the other vertebrate classes, i.e. the amphibians, reptiles, birds and mammals. Indeed, fishes can be considered by exclusion to be vertebrates that are not tetrapods (see Chapter 25: Introduction to Vertebrates). They are aquatic, gill- bearing, ectothermic ('cold-blooded') animals with a distinguishable head and, when present, digit-less limbs. Traditionally, fish have been arranged into three groups: ➵ Agnatha 1, the jawless fish (Myxini [hagfishes] and Hyperoartia [lampreys]); ➵ Chondrichthyes, the cartilaginous fish (sharks, skates and rays); ➵ Osteichthyes, the bony fish (Actinopterygii [ray-finned fishes] and Sarcopterygii [lobe-finned fishes]). This classification is adequate for general purposes, although Agnatha is paraphyletic and includes several groups of extinct jawless fishes. -
A Partial Braincase and Other Skeletal Remains of Oligocene Angel Sharks (Chondrichthyes, Squatiniformes) from Northwest Belgium, with Comments on Squatinoid Taxonomy
Contributions to Zoology, 85 (2) 147-171 (2016) A partial braincase and other skeletal remains of Oligocene angel sharks (Chondrichthyes, Squatiniformes) from northwest Belgium, with comments on squatinoid taxonomy Frederik H. Mollen1, 5, Barry W.M. van Bakel2, 3, John W.M. Jagt4 1 Elasmobranch Research, Rehaegenstraat 4, 2820 Bonheiden, Belgium 2 Oertijdmuseum De Groene Poort, Bosscheweg 80, 5283 WB Boxtel, The Netherlands 3 Naturalis Biodiversity Center, P.O. Box 9517, 2300 RA Leiden, The Netherlands 4 Natuurhistorisch Museum Maastricht, de Bosquetplein 6-7, 6211 KJ Maastricht, The Netherlands 5 E-mail: [email protected] Key words: chondrocranium, CT scanning, neurocranium, Pristiophorus, Squatina, vertebrae Abstract Orbital region (i.e., orbito-temporal or sphenoid region) ....................................................................................... 151 A detailed redescription of a chondrocranium from the basal Otic region (i.e., labyrinth or auditory region) ............... 152 Boom Clay Formation (Rupelian, Upper Oligocene) at the SVK Occipital region ...................................................................... 155 clay pit, Sint-Niklaas (province of Oost-Vlaanderen, Belgium), Results ............................................................................................. 157 previously assigned to the sawshark Pristiophorus rupeliensis, is Re-identification of chondrocranium ................................ 157 presented. The chondrocranium is re-identified as that of an an- Other angel shark skeletal -
Connecting the Chondrocranium: Biomechanics of the Suspensorium in Reptiles
70 (3): 275 – 290 © Senckenberg Gesellschaft für Naturforschung, 2020. 2020 VIRTUAL ISSUE on Recent Advances in Chondrocranium Research | Guest Editor: Ingmar Werneburg Connecting the chondrocranium: Biomechanics of the suspensorium in reptiles Alec T. Wilken 1, *, Kaleb C. Sellers 1, Ian N. Cost 2, Rachel E. Rozin 1, Kevin M. Middleton 1 & Casey M. Holliday 1 1 Department of Pathology and Anatomical Sciences, University of Missouri, M263, Medical Sciences Building, Columbia, MO, 65212, USA — 2 Department of Biology, Albright College, 13th and Bern Streets, Reading, PA, 19612, USA — * Corresponding author; atwxb6@ mail.missouri.edu Submitted February 07, 2020. Accepted June 8, 2020. Published online at www.senckenberg.de/vertebrate-zoology on June 16, 2020. Published in print on Q3/2020. Editor in charge: Ingmar Werneburg Abstract Gnathostomes all share the common challenge of assembling 1st pharyngeal arch elements and associated dermal bones (suspensorium) with the neurocranium into a functioning linkage system. In many tetrapods, the otic and palatobasal articulations between suspensorium and neurocranial elements form the joints integral for cranial kinesis. Among sauropsids, the otic (quadratosquamosal) joint is a key feature in this linkage system and shows considerable variability in shape, tissue-level construction and mobility among lineages of reptiles. Here we explore the biomechanics of the suspensorium and the otic joint in fve disparate species of sauropsids of different kinetic capacity (two squamates, one non-avian theropod dinosaur, and two avian species). Using 3D muscle modeling, comparisons of muscle moments, joint surface areas, cross-sectional geometries, and fnite element analysis, we characterize biomechanical differences in the resultants of protractor muscles, loading of otic joints, and bending properties of pterygoid bones. -
FIPAT-TA2-Part-2.Pdf
TERMINOLOGIA ANATOMICA Second Edition (2.06) International Anatomical Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TA2, PART II Contents: Systemata musculoskeletalia Musculoskeletal systems Caput II: Ossa Chapter 2: Bones Caput III: Juncturae Chapter 3: Joints Caput IV: Systema musculare Chapter 4: Muscular system Bibliographic Reference Citation: FIPAT. Terminologia Anatomica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, 2019 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Anatomica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput II: OSSA Chapter 2: BONES Latin term Latin synonym UK English US English English synonym Other 351 Systemata Musculoskeletal Musculoskeletal musculoskeletalia systems systems -
Ncomms6661.Pdf
ARTICLE Received 11 May 2014 | Accepted 24 Oct 2014 | Published 1 Dec 2014 DOI: 10.1038/ncomms6661 OPEN Evolutionary innovation and conservation in the embryonic derivation of the vertebrate skull Nadine Piekarski1,*, Joshua B. Gross1,*,w & James Hanken1 Development of the vertebrate skull has been studied intensively for more than 150 years, yet many essential features remain unresolved. One such feature is the extent to which embryonic derivation of individual bones is evolutionarily conserved or labile. We perform long-term fate mapping using GFP-transgenic axolotl and Xenopus laevis to document the contribution of individual cranial neural crest streams to the osteocranium in these amphibians. Here we show that the axolotl pattern is strikingly similar to that in amniotes; it likely represents the ancestral condition for tetrapods. Unexpectedly, the pattern in Xenopus is much different; it may constitute a unique condition that evolved after anurans diverged from other amphibians. Such changes reveal an unappreciated relation between life history evolution and cranial development and exemplify ‘developmental system drift’, in which interspecific divergence in developmental processes that underlie homologous characters occurs with little or no concomitant change in the adult phenotype. 1 Department of Organismic and Evolutionary Biology, Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, Massachusetts 02138, USA. * These authors contributed equally to this work. w Present address: Department of Biological Sciences, University of Cincinnati, Cincinnati, Ohio 45221, USA. Correspondence and requests for materials should be addressed to J.H. (email: [email protected]). NATURE COMMUNICATIONS | 5:5661 | DOI: 10.1038/ncomms6661 | www.nature.com/naturecommunications 1 & 2014 Macmillan Publishers Limited. -
Notes on the Development of the Chondrocranium of Polypterus Senegalus
Notes on the Development of the Chondrocranium of Polypterus Senegalus. By J. A. Moy-Thomas, B.A. Demonstrator in Zoology, the University, Leeds. With 16 Text-figures. CONTENTS. PAGE INTRODUCTION . 209 DESCRIPTION OF SPECIMENS . 210 EXPLANATION OF LETTBBING . 211 DISCUSSION OF RESULTS ...... 226 SUMMARY ...... 228 LIST OF LITERATURE ....... 228 INTRODUCTION THE chondrocranium of Polypterus is far better known in the later stages than in the earlier stages. Pollard (1892) described the cranial anatomy of a half-grown specimen, Budgett (1902) described a 30-mm. larva, and Lehn (1918) gave a detailed account of the neurocranium of a 55- and a 76-mm. specimen. The skull of the adult was first described by Traquair (1871); his description was added to by Bridge (1888), and finally an exhaustive description was given by Allis (1922). The chondrocranium of younger stages is, however, far less well known. The three existing young stages were briefly described by Graham Kerr (1907), and the mandibular and hyoid bars with their associated muscles of the same specimens were described by Edgeworth (1929). De Beer (1926) drew atten- tion to the important morphological characters in the chon- drocranium of Polypterus. Thus it can be seen that existing accounts of the development of the chondrocranium of P2 210 J. A. MOY-THOMAS Polypterus are mainly confined to the older stages, and the development of the young stages is only poorly known. At the suggestion of my friend and former tutor, Dr. G. R. de Beer, I determined to re-examine Budgett's material and to give a description of the chondrocranium, which would embody all the available information.