Anomalocaris

Total Page:16

File Type:pdf, Size:1020Kb

Anomalocaris Life of the Paleozoic Tuesday, November 22, 11 Life of the Paleozoic • Overview: • Cambrian, Vast expansion of shelly marine life forms and jawless fish • Ordovician - most modern phyla established • Late Paleozoic- land plants and vertebrates (tetrapods and amniotes) Tuesday, November 22, 11 Invertebrates • Marine environments • Nektic, planktic, benthic • Adaptions: • Epifaunal- animals living on the sea floor • Infaunal – animals that burrow into the sea floor Tuesday, November 22, 11 Early cambrian • Small Shelly fossils • Rarely more than a few millimeters long • A- Anabarella • B- Camanella • C- Aldanella • D- Sponge Spicule • E- Formitchella • F- Lapworthella Tuesday, November 22, 11 Early Soft-body fossils • The Burgess shale: • Most fossils reduced to shiny black impressions What type of fossilization is this? • Viewed as one of the most important finds of the fossil record • Altogether, over 60,000 species have been collected Tuesday, November 22, 11 The Burgess shale • Four Groups of Arthropods • Trilobites • Crustaceans • Scorpions • Insects • Sponges • Onycophorans • Crinoids • Sea Cucumbers • Chordates Tuesday, November 22, 11 Chordates • Shows evolution of early notochord • Notochord- dorsally situated nerve cord Why is this important? • Pikaia- small animal that has notochord and also shows evidence of v-shaped muscle bands (this indicated sinosoidal swimming motion THESE ANIMALS ARE ANCESTORS TO ALL MODERN VERTEBRATES Tuesday, November 22, 11 Other Notable Fossils • Anomalocaris- fierce predator over 50cm long (~2ft) • Opabinia- five eyes, flexible nozzle • Hallucigenia- seven pairs of legs, seven dorsal spines, claws, cylindrical trunk. (Considered to be a onycophoran) • Marrella- Four spines extended back from cephalon The most common arthropod found in the burgess shale Tuesday, November 22, 11 Tuesday, November 22, 11 Protista (unicellular groups) • Foraminifera (Calcerous Microfossils) • Range from Cambrian to present • More numerous and varied by Carboniferous • Global distribution during Pennsylvanian-Permian • Radiolarians (Siliceous Microfossils) • Range early Paleozoic to present • Most abundant in Mesozoic rocks Tuesday, November 22, 11 Porifera • Pore-bearing animals • Appear to evolved from colonial flagellated unicellular creatures • Cambrian representatives of all but one modern class are known as fossils (Have not changed much) Tuesday, November 22, 11 Fossil Porifera Modern Sponges Tuesday, November 22, 11 Corals and Cnidarians • Main Groups • Sea Anemonies • Sea Fans • Jelly Fish • Hydra • Reef-forming Corals Tuesday, November 22, 11 Brachiopods • Most abundant, diverse, and useful Paleozoic fossil group • Braciopods are bivalves, however, each valve (shell) differs in shape and size. • Unlike clam shell which can be considered right and left brachiopod shells are distinguished between dorsal and ventral. • Most valves are made of Calcium Carbonate. • Ornamented with radial ridges, grooves, spines, nodes and growth lines. Tuesday, November 22, 11 Groups of Brachiopod • Articulate Brachiopods • Valves are hinged along the posterior margin and are prevented by sliding sideways by teeth and grooves • Inarticulate Brachiopods • Lack a definite hinge structure • Valves held together by muscle • Both are filter feeders attached to sea floor by fleshy stalk (pedicle) • Lophophore: hair like structures that circulate water and food toward mouth Tuesday, November 22, 11 Fossil Brachiopods Tuesday, November 22, 11 Mollusks • Gastropods (snails) • Earliest forms constructed small conical shells, by late Cambrian/early Ordovician most had developed the more recognizable coiled shell. • By Pennsylvanian gastropods extremely abundant and even air-breathing species had developed • Cephalopods- may be the most advanced and complex of all invertebrates Tuesday, November 22, 11 Cephalopods • Represented today by: • Squid • Cuttlefish • Octopods • Chambered Nautilus Tuesday, November 22, 11 Ammonites • Goniatites, the first ammonite, appears during the Devonian • Other Ammonites Tuesday, November 22, 11 Arthropods • Includes: • Lobsters • Spiders • Insects • All animals that have chitonous exterior skeletons, segmented bodies, and paired,jointed appendages Tuesday, November 22, 11 Trilobites Tuesday, November 22, 11 Trilobites Tuesday, November 22, 11 Eurypterids • Scorpion like bodies • Found in Ordovician- permian Marine and Brackish facies • Recent finds suggest that some eurypterids reached a length of 9ft. Tuesday, November 22, 11 Eurypterids • Scorpion like bodies • Found in Ordovician- permian Marine and Brackish facies • Recent finds suggest that some eurypterids reached a length of 9ft. Tuesday, November 22, 11 Echinoderms • Spiny-skinned animals • Five way symmetry • Exclusively marine- typically bottom dwelling, either attached or mobile • Group includes • Starfish • Sea Urchins • Crinoids • Crystoids Tuesday, November 22, 11 Echinoderms • Appear to have developed during late proterozoic • Ediacaran, also had five way symmetry • Stemmed or stalked echinoderms first occur in mid cambrian (not abundant until Ordovician) Tuesday, November 22, 11 Echinoderms • Appear to have developed during late proterozoic • Ediacaran, also had five way symmetry • Stemmed or stalked echinoderms first occur in mid cambrian (not abundant until Ordovician) Tuesday, November 22, 11 Continental Invertebrates • Fossil evidence is less complete Why? • However as plants begin to invade continent so do animals • Record begins with possible Millipede tracks in Ordovician rocks. • Body Fossils of Centipedes and Millipedes occur in Silurian rock • In New York, Devonian rocks have yielded fossil centipedes, spiders and other wingless arthropods • Insects do not become common until the late Missipian • The Pennsylvanian witnessed the arrival of flying insects like the dragon fly • Coal swamps from the Pennsylvanian yielded a dragon fly with a wingspan of over 2 ft. Tuesday, November 22, 11 Vertebrates • Evolution of Fish • Dermal Plates (Upper Cambrian) • Scales and Plates (Ordovician) • Four Taxonomic classes: • Agnatha (jawless fish) • Acanthodii (Archaic jawed fish) • Chondrichthyes (cartilaginous fish) • Osteichthyes (Bony fish) Tuesday, November 22, 11 Agnatha • Earliest known (early Cambrian) species include Theolodus, Jamoytius, Pteraspis (armored) and Hemicyclapsis Tuesday, November 22, 11 Acanthodii • Arose during Silurian • Most numerous during Devonian • Extinct during Permian Tuesday, November 22, 11 Chondrichthyes • Late Devonian to Present • Represent shark, rays, and skates • Cladoselache- late paleozoic shark Tuesday, November 22, 11 Osteichthyes • Bony Fish can be divided into two groups • Actinoptergians • Lack a muscular base to their paired fins • Also lack nasal passage to the throat • Sarcoptergians • Had sturdy, fleshy lobe-fins • A pair of openings in upper mouth that led to external nostrils • Were able to rise to surface to take in air that was passed onto functional lungs (Lung Fish) Tuesday, November 22, 11 Sarcoptergians • Two major roups lived during the Devonian • Dipnoans • Dipnoans- include some present day freshwater living species of lungfish in Australia and Africa • Crossopterygians • Because of the pattern of skull elements, arrangement of bones in their fins, and the structure of their teeth, Crossopterygians are considered to be the ancestor of the earliest land inhabitants (tetrapods). Tuesday, November 22, 11 Sarcoptergians • Two major roups lived during the Devonian • Dipnoans • Dipnoans- include some present day freshwater living species of lungfish in Australia and Africa • Crossopterygians • Because of the pattern of skull elements, arrangement of bones in their fins, and the structure of their teeth, Crossopterygians are considered to be the ancestor of the earliest land inhabitants (tetrapods). Tuesday, November 22, 11 Crossopterygians & Tetrapods Tuesday, November 22, 11 Tetrapods • Tetrapods are four- footed vertebrates • Amphibia, Reptilia, Mammalia Tuesday, November 22, 11 Tetrapods • First to come ashore did not leave the water completely • Amphibians • Return to water to lay eggs • From eggs come fish-like larvae that develop in water • Number of changes had to accompany the shift to land Tuesday, November 22, 11 Shift to land • A three chambered heart developed • Limb and girdle bones had to be modified to overcome gravity • Spinal column became more sturdy but yet flexible • To better assist hearing the Hyomandibular (fish) transformed into an ear ossicle-the stapes Tuesday, November 22, 11 Fossil Record of Basal Tetrapods • Late Devonian • Ichthyostegids • Retained many features of their fish ancestor • Tail fin • Bony gill covers • Fish-like vertrbae • Skull bones similar to crossopterygians • Labyrinthic folding of enamel • Due to this following species are referred to as Labyrinthodonts • During the Carboniferous large numbers of these Labyrinthodonts wallowed in swamps and streams Tuesday, November 22, 11 Tuesday, November 22, 11 Evolution of the Tetrapods • Development of the amniotic egg • These animals are referred to as amniotes • During the Carboniferous Amniotes diverged into two groups • Reptilia: anapsids, diapsids, and archosaurs • Synapsids- Mammal-like reptiles Tuesday, November 22, 11 Synapsids • Although the synapsids are called “mammal- like reptiles, cladistic analysis shows that they are not reptiles • Some sported big sail-like structures (pelycosaurs) • Varied group • Carnivores: Dimetrodon • Herbivores: Edaphosaurus Tuesday, November 22, 11 Synapsids • Although the synapsids are called
Recommended publications
  • Constraints on the Timescale of Animal Evolutionary History
    Palaeontologia Electronica palaeo-electronica.org Constraints on the timescale of animal evolutionary history Michael J. Benton, Philip C.J. Donoghue, Robert J. Asher, Matt Friedman, Thomas J. Near, and Jakob Vinther ABSTRACT Dating the tree of life is a core endeavor in evolutionary biology. Rates of evolution are fundamental to nearly every evolutionary model and process. Rates need dates. There is much debate on the most appropriate and reasonable ways in which to date the tree of life, and recent work has highlighted some confusions and complexities that can be avoided. Whether phylogenetic trees are dated after they have been estab- lished, or as part of the process of tree finding, practitioners need to know which cali- brations to use. We emphasize the importance of identifying crown (not stem) fossils, levels of confidence in their attribution to the crown, current chronostratigraphic preci- sion, the primacy of the host geological formation and asymmetric confidence intervals. Here we present calibrations for 88 key nodes across the phylogeny of animals, rang- ing from the root of Metazoa to the last common ancestor of Homo sapiens. Close attention to detail is constantly required: for example, the classic bird-mammal date (base of crown Amniota) has often been given as 310-315 Ma; the 2014 international time scale indicates a minimum age of 318 Ma. Michael J. Benton. School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, U.K. [email protected] Philip C.J. Donoghue. School of Earth Sciences, University of Bristol, Bristol, BS8 1RJ, U.K. [email protected] Robert J.
    [Show full text]
  • Sedimentology and Palaeontology of the Withycombe Farm Borehole, Oxfordshire, UK
    Sedimentology and Palaeontology of the Withycombe Farm Borehole, Oxfordshire, England By © Kendra Morgan Power, B.Sc. (Hons.) A thesis submitted to the School of Graduate Studies in partial fulfillment of the requirements for the degree of Master of Science Department of Earth Sciences Memorial University of Newfoundland May 2020 St. John’s Newfoundland Abstract The pre-trilobitic lower Cambrian of the Withycombe Formation is a 194 m thick siliciclastic succession dominated by interbedded offshore red to purple and green pyritic mudstone with minor sandstone. The mudstone contains a hyolith-dominated small shelly fauna including: orthothecid hyoliths, hyolithid hyoliths, the rostroconch Watsonella crosbyi, early brachiopods, the foraminiferan Platysolenites antiquissimus, the coiled gastropod-like Aldanella attleborensis, halkieriids, gastropods and a low diversity ichnofauna including evidence of predation by a vagile infaunal predator. The assemblage contains a number of important index fossils (Watsonella, Platysolenites, Aldanella and the trace fossil Teichichnus) that enable correlation of strata around the base of Cambrian Stage 2 from Avalonia to Baltica, as well as the assessment of the stratigraphy within the context of the lower Cambrian stratigraphic standards of southeastern Newfoundland. The pyritized nature of the assemblage has enabled the study of some of the biota using micro-CT, augmented with petrographic studies, revealing pyritized microbial filaments of probable giant sulfur bacteria. We aim to produce the first complete description of the core and the abundant small pyritized fossils preserved in it, and develop a taphonomic model for the pyritization of the “small” shelly fossils. i Acknowledgements It is important to acknowledge and thank the many people who supported me and contributed to the successful completion of this thesis.
    [Show full text]
  • Shell Microstructures in Early Mollusks
    Vol. XLII(4): 2010 THE FESTIVUS Page 43 SHELL MICROSTRUCTURES IN EARLY MOLLUSKS MICHAEL J. VENDRASCO1*, SUSANNAH M. PORTER1, ARTEM V. KOUCHINSKY2, GUOXIANG LI3, and CHRISTINE Z. FERNANDEZ4 1Institute for Crustal Studies, University of California, Santa Barbara, CA, 93106, USA 2Department of Palaeozoology, Swedish Museum of Natural History, Box 50007, SE-104 05 Stockholm, Sweden 3LPS, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, 39 East Beijing Road, Nanjing 210008, P.R. China, 414601 Madris Ave., Norwalk, CA 90650, USA Abstract: Shell microstructures in some of the oldest known mollusk fossils (from the early to middle Cambrian Period; 542 to 510 million years ago) are diverse, strong, and in some cases unusual. We herein review our recent work focused on different aspects of shell microstructures in Cambrian mollusks, briefly summarizing some of the major conclusions from a few of our recent publications and adding some new analysis. Overall, the data suggest that: (1) mollusks rapidly evolved disparate shell microstructures; (2) early mollusks had a complex shell with a different type of shell microstructure in the outer layer than in the inner one; (3) the modern molluscan biomineralization system, with precise control over crystal shapes and arrangements in a mantle cavity bounded by periostracum, was already in place during the Cambrian; (4) shell microstructure data provide a suite of characters useful in phylogenetic analyses of mollusks and mollusk-like Problematica, allowing better determination
    [Show full text]
  • Terreneuvian Stratigraphy and Faunas from the Anabar Uplift, Siberia
    Terreneuvian stratigraphy and faunas from the Anabar Uplift, Siberia ARTEM KOUCHINSKY, STEFAN BENGTSON, ED LANDING, MICHAEL STEINER, MICHAEL VENDRASCO, and KAREN ZIEGLER Kouchinsky, A., Bengtson, S., Landing, E., Steiner, M., Vendrasco, M., and Ziegler, K. 2017. Terreneuvian stratigraphy and faunas from the Anabar Uplift, Siberia. Acta Palaeontologica Polonica 62 (2): 311‒440. Assemblages of mineralized skeletal fossils are described from limestone rocks of the lower Cambrian Nemakit-Daldyn, Medvezhya, Kugda-Yuryakh, Manykay, and lower Emyaksin formations exposed on the western and eastern flanks of the Anabar Uplift of the northern Siberian Platform. The skeletal fossil assemblages consist mainly of anabaritids, molluscs, and hyoliths, and also contain other taxa such as Blastulospongia, Chancelloria, Fomitchella, Hyolithellus, Platysolenites, Protohertzina, and Tianzhushanella. The first tianzhushanellids from Siberia, including Tianzhushanella tolli sp. nov., are described. The morphological variation of Protohertzina anabarica and Anabarites trisulcatus from their type locality is documented. Prominent longitudinal keels in the anabaritid Selindeochrea tripartita are demon- strated. Among the earliest molluscs from the Nemakit-Daldyn Formation, Purella and Yunnanopleura are interpreted as shelly parts of the same species. Fibrous microstructure of the outer layer and a wrinkled inner layer of mineralised cuticle in the organophosphatic sclerites of Fomitchella are reported. A siliceous composition of the globular fossil Blastulospongia
    [Show full text]
  • Constraining the Ediacaran-Cambrian Boundary in South China Using Acanthomorphic Acritarchs and Plaeopascichnus Fossils Kenneth Hugh O’Donnell
    Constraining the Ediacaran-Cambrian boundary in South China using acanthomorphic acritarchs and Plaeopascichnus fossils Kenneth Hugh O’Donnell Thesis submitted to the faculty of Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Master of Science In Geosciences S. Xiao, Committee Chair Kenneth A. Eriksson Patricia E. Dove May 7, 2013 Blacksburg, VA Keywords: Biostratigraphy; Heliosphaeridium; Palaeopascichnus; acritarchs; acanthomorphic; Yanjiahe; Liuchapo; Niutitang; Ediacaran; Cambrian; South China Copyright 2013 Constraining the Ediacaran-Cambrian boundary in South China using acanthomorphic acritarchs and Palaeopascichnus fossils Kenneth O’Donnell ABSTRACT The Ediacaran-Cambrian boundary is arguably the most critical transition in Earth history. This boundary is currently defined by the GSSP (Global Stratotype Section and Point) at Fortune Head (Newfoundland, Canada) at a point that was once regarded as the first appearance of the branching trace fossil Treptichnus pedum. However, T. pedum has been subsequently found below the GSSP, and its distribution is largely restricted to sandstone facies where chemostratigraphic correlation tools are difficult to apply. Thus, the stratigraphic value of the Fortune Head GSSP has come under scrutiny, and there is a need to search for an alternative definition of this boundary using other biostratigraphic criteria. Investigations of acanthomorphic acritarchs in basal Cambrian strata of South China suggest that these microfossils may
    [Show full text]
  • Phylogenesis and the System of the Cambrian Univalved Mollusks P
    Paleontological Journal, Vol. 36, No. 1, 2002, pp. 25–36. Translated from Paleontologicheskii Zhurnal, No. 1, 2002, pp. 27–39. Original Russian Text Copyright © 2002 by Parkhaev. English Translation Copyright © 2002 by åÄIä “Nauka /Interperiodica” (Russia). Phylogenesis and the System of the Cambrian Univalved Mollusks P. Yu. Parkhaev Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya ul. 123, Moscow, 117997 Russia Received May 30, 2000 Abstract—The history of the study and the development of ideas about the systematic position of the Cambrian univalved mollusks is reviewed. On the basis of the functional morphology of shells (Parkhaev, 2000a, 2001a), the phylogenetic scenario of the evolution of the group is reconstructed and its systematics is determined. Sev- eral new taxa are described, i.e., Archaeobranchia subclas. nov., Khairkhaniiformes ordo nov., Igarkiellidae fam. nov., Trenellidae fam. nov., Watsonellinae subfam. nov., and Runnegarella gen. nov. HISTORY OF THE STUDY OF THE CAMBRIAN This new method of fossil preparation resulted in an UNIVALVED MOLLUSKS increased number of publications on the Cambrian fauna and, therefore, in an increased number of described taxa The first mollusks from the Cambrian deposits were of small shelly fossils (including mollusks). described in the mid-19th century by Hall and d’Orbigny. In the second half of the 19th century, the The number of specialists that studied the Cambrian number of taxa of the Cambrian mollusks significantly mollusks also increased, and different, in some cases increased due to the numerous publications focused on even contradictory, opinions on the systematics of this the fauna of that geological period (Barrande, 1867; group appeared.
    [Show full text]
  • U.S. Oeoxogijcal SUB.Vklir PROFESSIONAL PAPEE AVAILABILITY of BOOKS and MAPS of the U.S
    f~\r/% OI U.S. OEOXOGIjCAL SUB.VKlir PROFESSIONAL PAPEE AVAILABILITY OF BOOKS AND MAPS OF THE U.S. GEOLOGICAL SURVEY Instructions on ordering publications of the U.S. Geological Survey, along with prices of the last offerings, are given in the cur­ rent-year issues of the monthly catalog "New Publications of the U.S. Geological Survey." Prices of available U.S. Geological Sur­ vey publications released prior to the current year are listed in the most recent annual "Price and Availability List." Publications that are listed in various U.S. Geological Survey catalogs (see back inside cover) but not listed in the most recent annual "Price and Availability List" are no longer available. Prices of reports released to the open files are given in the listing "U.S. Geological Survey Open-File Reports," updated month­ ly, which is for sale in microfiche from the U.S. Geological Survey, Books and Open-File Reports Section, Federal Center, Box 25425, Denver, CO 80225. Reports released through the NTIS may be obtained by writing to the National Technical Information Service, U.S. Department of Commerce, Springfield, VA 22161; please include NTIS report number with inquiry. Order U.S. Geological Survey publications by mail or over the counter from the offices given below. BY MAIL n , OVER THE COUNTER Books Books Professional Papers, Bulletins, Water-Supply Papers, Techniques of Water-Resources Investigations, Circulars, publications of general in- Books of the U.S. Geological Survey are available over the terest (such as leaflets, pamphlets, booklets), single copies of Earthquakes counter at the following Geological Survey Public Inquiries Offices, all & Volcanoes, Preliminary Determination of Epicenters, and some mis- of which are authorized agents of the Superintendent of Documents: cellaneous reports, including some of the foregoing series that have gone out of print at the Superintendent of Documents, are obtainable by mail from WASHINGTON, D.C.-Main Interior Bldg., 2600 corridor, 18th and CSts.,NW.
    [Show full text]
  • Terreneuvian Stratigraphy and Faunas from the Anabar Uplift, Siberia
    Terreneuvian stratigraphy and faunas from the Anabar Uplift, Siberia ARTEM KOUCHINSKY, STEFAN BENGTSON, ED LANDING, MICHAEL STEINER, MICHAEL VENDRASCO, and KAREN ZIEGLER Kouchinsky, A., Bengtson, S., Landing, E., Steiner, M., Vendrasco, M., and Ziegler, K. 2017. Terreneuvian stratigraphy and faunas from the Anabar Uplift, Siberia. Acta Palaeontologica Polonica 62 (2): 311‒440. Assemblages of mineralized skeletal fossils are described from limestone rocks of the lower Cambrian Nemakit-Daldyn, Medvezhya, Kugda-Yuryakh, Manykay, and lower Emyaksin formations exposed on the western and eastern flanks of the Anabar Uplift of the northern Siberian Platform. The skeletal fossil assemblages consist mainly of anabaritids, molluscs, and hyoliths, and also contain other taxa such as Blastulospongia, Chancelloria, Fomitchella, Hyolithellus, Platysolenites, Protohertzina, and Tianzhushanella. The first tianzhushanellids from Siberia, including Tianzhushanella tolli sp. nov., are described. The morphological variation of Protohertzina anabarica and Anabarites trisulcatus from their type locality is documented. Prominent longitudinal keels in the anabaritid Selindeochrea tripartita are demon- strated. Among the earliest molluscs from the Nemakit-Daldyn Formation, Purella and Yunnanopleura are interpreted as shelly parts of the same species. Fibrous microstructure of the outer layer and a wrinkled inner layer of mineralised cuticle in the organophosphatic sclerites of Fomitchella are reported. A siliceous composition of the globular fossil Blastulospongia
    [Show full text]
  • Pelagiella Exigua, an Early Cambrian Stem Gastropod With
    [Palaeontology, Vol. 63, Part 4, 2020, pp. 601–627] PELAGIELLA EXIGUA,ANEARLYCAMBRIAN STEM GASTROPOD WITH CHAETAE: LOPHOTROCHOZOAN HERITAGE AND CONCHIFERAN NOVELTY by ROGER D. K. THOMAS1 , BRUCE RUNNEGAR2 and KERRY MATT3 1Department of Earth & Environment, Franklin & Marshall College, PO Box 3003, Lancaster, PA 17604-3003, USA; [email protected] 2Department of Earth, Planetary, & Space Sciences & Molecular Biology Institute, University of California, Los Angeles, CA 90095-1567, USA 3391 Redwood Drive, Lancaster, PA 17603-4232, USA Typescript received 8 October 2018; accepted in revised form 4 December 2019 Abstract: Exceptionally well-preserved impressions of two appendages were anterior–lateral, based on their probable bundles of bristles protrude from the apertures of small, functions, prompts a new reconstruction of the anatomy of spiral shells of Pelagiella exigua, recovered from the Kinzers Pelagiella, with a mainly anterior mantle cavity. Under this Formation (Cambrian, Stage 4, ‘Olenellus Zone’, c. 512 Ma) hypothesis, two lateral–dorsal grooves, uniquely preserved of Pennsylvania. These impressions are inferred to represent in Pelagiella atlantoides, are interpreted as sites of attach- clusters of chitinous chaetae, comparable to those borne by ment for a long left ctenidium and a short one, anteriorly annelid parapodia and some larval brachiopods. They pro- on the right. The orientation of Pelagiella and the asymme- vide an affirmative test in the early metazoan fossil record try of its gills, comparable to features of several living veti- of the inference, from phylogenetic analyses of living taxa, gastropods, nominate it as the earliest fossil mollusc known that chitinous chaetae are a shared early attribute of the to exhibit evidence of the developmental torsion character- Lophotrochozoa.
    [Show full text]
  • Department of Geology G.D.C Anantnag (Boys) Semester 6
    Department of Geology G.D.C Anantnag (Boys) Semester 6 Unit-1. Origin and Evolution of Life Origin of life: It is generally agreed that all life today evolved by common descent from a single primitive lifeform. We do not know how this early form came about, but scientists think it was a natural process which took place perhaps 3,900 million years ago. Origin of earth and its atmosphere: Earth is believed to have formed about 5 billion years ago. In the first 500 million years a dense atmosphere emerged from the vapor and gases that were expelled during degassing of the planet's interior. These gases may have consisted of hydrogen (H2), water vapor, methane (CH4) , and carbon oxides. Prior to 3.5 billion years ago the atmosphere probably consisted of carbon dioxide (CO2), carbon monoxide (CO), water (H2O), nitrogen (N2), and hydrogen.The hydrosphere was formed 4 billion years ago from the condensation of water vapor, resulting in oceans of water in which sedimentation occurred. Evolution is a branch of science deals with the unfolding of new and complex species from simple species. There are different plants and the animals which evolve in different ways in different habit, habitat or adaption. In general evolution is a dynamic process in which gradual change of body morphology takes place, after long period of time convert into more and more complex animal. Scientific hypothesis- Chemical evolution of life: Chemical evolution describes chemical changes on the primitive Earth that gave rise to the first forms of life. The first living things on Earth were prokaryotes with a type of cell similar to present-day bacteria.
    [Show full text]
  • Paleontology Material Unit: II Phyllum Mollusca
    Paleontology material Unit: II Phyllum Mollusca Pelecypoda. Morphology of the pelecypoda is the Shells inequilateral, mequivalve, middlesized, varying in shape from rounded, through subtriangular to oval, cemented to the substratum by the right valve. External ornamentation consists of numerous, fine growth lines, concentrical lamellae and radial ribs. Shell margin finely denticulate. The right valve convex, the greatest convexity being recorded at 1/3 of the distance from the ventral margin. Umbo not prominent, narrow, with a small, terminally situated attachment area or wide, straight, with a large area which occupies smaller or larger subumbonal part of valve. Ribs numerous, their number increases, both by bifurcation and intercalation, SOME JURASSIC SPECIES OF PLICATULA (PELECYPODA) 225 from 12 to more than 30. The height and thickness of ribs increase with the growth of valve from 0.5 to 1.5 mm. On some valves ribs are more numerous but thinner and lower and on some others less numerous but thicker and higher. The surface of ribs is uneven and slightly knobby. Usually, thicker swellings occur at intersections of ribs with concentrical growth lines . The intervals between ribs are usually twice as wide as ribs. According to differences in ornamentation of valves, the following two types of forms may be distinguished: in one of them, valves have well-developed ribs and slightly marked growth lines, in the othe!f, valves have low, fine ribs amid thkk, ,sometimes soaly, corncentrical lamellae. Few valves have a combined, costate-lamellar ornamentation. In the latter case, both ribs and lamellae are equally developed . The left valve convex the most so at a 1/3 of a distance from the ventral margin, in the suibumbonal part slightly convex or flattened.
    [Show full text]
  • Muscle Scars in Euomphaline Gastropods from the Ordovician of Baltica
    Estonian Journal of Earth Sciences, 2019, 68, 2, 88–100 https://doi.org/10.3176/earth.2019.08 Muscle scars in euomphaline gastropods from the Ordovician of Baltica John S. Peel Department of Earth Sciences (Palaeobiology), Uppsala University, Villavägen 16, SE-75236 Uppsala, Sweden; [email protected] Received 8 March 2019, accepted 16 April 2019, available online 9 May 2019 Abstract. A discrete pair of muscle scars is described for the first time on the umbilical wall of the open-coiled, hyperstrophic ophiletoidean gastropod Asgardispira, a close relative of the widely distributed Lytospira, from the middle Ordovician of the eastern Baltica. In a unique specimen of the euomphaloidean Lesueurilla of similar age and derivation, the muscles have coalesced into a single scar. A pair of pedal retractor muscles is characteristic of several major groups of gastropods both in the Lower Palaeozoic and at the present day, and was likely an ancestral character of the class. The consolidation of muscle attachment to a single site may reflect the tightening of the logarithmic spiral of the shell and is probably related to the increasing development of anisostrophic coiling and shell re-orientation during gastropod evolution. Key words: gastropods, muscle scars, Ordovician, Baltica. INTRODUCTION However, the concentration of attachment sites into distinct muscle sites has been described by Parkhaev Snails are attached to their shells by muscles which (2002, 2014) and in the strongly coiled, anisostrophic, often leave distinct attachment scars on the shell interior. pelagiellids (Runnegar 1981). Attachment scars are Muscle scars may be readily visible in limpets and other also described in morphologically similar Palaeozoic cap-shaped shells but they are usually difficult to see gastropod limpets such as Archinacella Ulrich & Scofield, in coiled shells where the muscle attachment site lies 1897, Floripatella Yochelson, 1988, Guelphinacella Peel, on the adaxial surface at some distance within the 1990 and Barrandicella Peel & Horný, 1999.
    [Show full text]