Phylum: Mollusca B.Sc I (Hons + Subsi)
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Monoplacophoran Limpet
16 McLean: Monoplacophoran Limpet FIGURES 17-21. Neopilinid radular ribbons, magnifications adjusted to show a similar number of teeth rows. FIGURE 17, Vema (Vema) ewingi. intact ribbon with teeth aligned (LACM 65-11, 6200 m. 110 mi. W of Callao. Pern. R/V ANTON BRUUN, 24 November 1965). FIGURE 18, Vema (Vema) ewingi. another portion of same ribbon with lateral teeth turned to the side. FIGURE 19. Neopilina veleronis. intact ribbon of paratype, teeth not aligned (AHF 603, 2730-2769 m, 30 mi. W of Natividad Island. Baja California, Mexico). FIGURE 20, Vema (Laevipilina) hyalina new species, intact ribbon with teeth aligned, focused on shafts of lateral teeth (LACM 19148). FIGURE 21, Vema (Laevipilina) hyalina, same ribbon, focused on fringe of first marginal teeth. instead of the highly reduced condition in these two species. Al- small-sized species have similar teeth. Radular differences among though the first lateral of N. veleronis is somewhat larger than it the species examined are quantitative rather than qualitative, sup- is in the other two species, that of V. hyalina is still the larger. porting placement of the four species in the same family. A study The fringed first marginal of V. hyalina is much broader than in of the radulae of the other three living species of neopilinids N. veleronis. Only in V. hyalina is the fringed tooth so broad that should reveal further specific differences. it overlaps the opposite member in the central part of the ribbon. The radula of neopilinid monoplacophorans is very similar to The second and third laterals of V. -
Deep-Sea Video Technology Tracks a Monoplacophoran to the End of Its Trail (Mollusca, Tryblidia)
Deep-sea video technology tracks a monoplacophoran to the end of its trail (Mollusca, Tryblidia) Sigwart, J. D., Wicksten, M. K., Jackson, M. G., & Herrera, S. (2018). Deep-sea video technology tracks a monoplacophoran to the end of its trail (Mollusca, Tryblidia). Marine Biodiversity, 1-8. https://doi.org/10.1007/s12526-018-0860-2 Published in: Marine Biodiversity Document Version: Publisher's PDF, also known as Version of record Queen's University Belfast - Research Portal: Link to publication record in Queen's University Belfast Research Portal Publisher rights Copyright 2018 the authors. This is an open access article published under a Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. General rights Copyright for the publications made accessible via the Queen's University Belfast Research Portal is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The Research Portal is Queen's institutional repository that provides access to Queen's research output. Every effort has been made to ensure that content in the Research Portal does not infringe any person's rights, or applicable UK laws. If you discover content in the Research Portal that you believe breaches copyright or violates any law, please contact [email protected]. Download date:06. Oct. 2021 Deep-sea video technology tracks a monoplacophoran to the end of its trail (Mollusca, Tryblidia) Sigwart, J. -
Foraging Tactics in Mollusca: a Review of the Feeding Behavior of Their Most Obscure Classes (Aplacophora, Polyplacophora, Monoplacophora, Scaphopoda and Cephalopoda)
Oecologia Australis 17(3): 358-373, Setembro 2013 http://dx.doi.org/10.4257/oeco.2013.1703.04 FORAGING TACTICS IN MOLLUSCA: A REVIEW OF THE FEEDING BEHAVIOR OF THEIR MOST OBSCURE CLASSES (APLACOPHORA, POLYPLACOPHORA, MONOPLACOPHORA, SCAPHOPODA AND CEPHALOPODA) Vanessa Fontoura-da-Silva¹, ², *, Renato Junqueira de Souza Dantas¹ and Carlos Henrique Soares Caetano¹ ¹Universidade Federal do Estado do Rio de Janeiro, Instituto de Biociências, Departamento de Zoologia, Laboratório de Zoologia de Invertebrados Marinhos, Av. Pasteur, 458, 309, Urca, Rio de Janeiro, RJ, Brasil, 22290-240. ²Programa de Pós Graduação em Ciência Biológicas (Biodiversidade Neotropical), Universidade Federal do Estado do Rio de Janeiro E-mails: [email protected], [email protected], [email protected] ABSTRACT Mollusca is regarded as the second most diverse phylum of invertebrate animals. It presents a wide range of geographic distribution patterns, feeding habits and life standards. Despite the impressive fossil record, its evolutionary history is still uncertain. Ancestors adopted a simple way of acquiring food, being called deposit-feeders. Amongst its current representatives, Gastropoda and Bivalvia are two most diversely distributed and scientifically well-known classes. The other classes are restricted to the marine environment and show other limitations that hamper possible researches and make them less frequent. The upcoming article aims at examining the feeding habits of the most obscure classes of Mollusca (Aplacophora, Polyplacophora, Monoplacophora, Scaphoda and Cephalopoda), based on an extense literary research in books, journals of malacology and digital data bases. The review will also discuss the gaps concerning the study of these classes and the perspectives for future analysis. -
THE ANATOMY of NEOPILINA GALATHEAE LEMCHE. 1957 (Molluscs Tryblidiacea)
THE ANATOMY OF NEOPILINA GALATHEAE LEMCHE. 1957 (Molluscs Tryblidiacea) By HENNING LEMCHE and KARL GEORG WINGSTRAND Zoological Museum. Institute for Comparative Anatomy and Zoological University of Copenhagen Technique. University of Copenhagen CONTENTS Introduction ......................... 10 The Lateral Nerve Cords ................ 47 Material and Methods .................... 10 The Pedal Nerve Cords .................. 48 General Description ..................... 12 The Nerves to the Postoral Tentacles and to The Outer Epithelia ..................... 13 the Statocysts ....................... 49 Slightly Specialized Epithelia .............. 13 Comparative Remarks .................. 50 Specialized Ciliated Epithelia .............. 13 Senseorgans ........................ 50 Glandular Epithelia .................... 14 Connective Tissue and Blood Cells ............ 51 Cuticle-Carrying Epithelia ................ 14 The Vascular System .................... 52 The Shell and the Pallial Fold .............. 15 General Morphology .................. 52 The Gills ........................... 19 The Efferent Gill Vessels and the Arterial Mantle TheFoot ........................... 21 Sinuses .......................... 52 The Mouth Region ...................... 22 The Atria .......................... 52 The Preoral Tentacles .................. 22 The Ventricles ....................... 53 The Velum ......................... 23 The Atrio-Ventricular Ostia ............... 53 The Postoral Tentacle Tufts ............... 23 The Aorta ........................ -
E D I T O R I a L
E D I T O R I A L THE POTENCY OF PREVAILING CONCEPTS In a recent public discussion on a state university campus in the eastern United States, a genetics professor who teaches the basic course in evolution at that institution stated that the developments in molecular biology have established that Charles Darwin was wrong in the mechanism he proposed for an evolutionary development of life. This professor went on to say that although there is at present no evidence that clearly supports an origin and development of life by naturalistic processes, there is no justification for saying that an evolutionary or non-theistic explanation for life is incorrect; the task facing the scientific community is to find new explanations concerning how evolution did occur, not to abandon the concept. Three aspects of these comments deserve consideration. First is the recognition that despite what are often strong claims to the contrary, the accumulation of scientific evidence has been increasingly unfavorable to mechanistic evolutionary concepts of origin. Professor D. E. Green of the Institute for Enzyme Research at the University of Wisconsin and Dr. R. F. Goldberger, chief of the Biosynthesis and Control Section, Laboratory of Chemical Biology, U.S. National Institutes of Health, in their book Molecular Insights Into the Living Process say that “...the macromolecule-to-cell transition is a jump of fantastic dimensions which lies beyond the range of testable hypotheses. In this area all is conjecture. The available facts do not provide a basis for postulating that cells arose on this planet.”1 Dr. John Keosian of the Marine Biological Laboratory at Woods Hole, Massachusetts, at an international conference on the origin of life held in Barcelona, Spain, in June 1973, said “...the simplest heterotrophic [obtains food from outside sources] cell is an intricate structural and metabolic unit of harmoniously coordinated parts and chemical pathways. -
Economic Importance of Mollusca Molluscs Are of General Importance Within Food Chains and As Members of Ecosystems
Page-1 M.Sc. 1st Semester ; Course Code: Zoo-02-CR; Unit: III (3.2) Modification of foot in molluscs Brief Introduction: Phylum Mollusca is characterised by the pronounced development of musculature known as the foot. It is the locomotory organ in Molluscs. This organ is quite uncommon and strange to others. It is regarded as the remnant of the „dermo-muscular tube‟ of the ancestral form whose ventral side became greatly developed as an adaptation for creeping movement and the dorsal portion be- came degenerated. In Mollusca, the foot originates at first as the ventral or ventro-lateral elevation of the ectodermal cells behind the mantle emerging in Veliger and some other larval forms, later the mesodermal cells incorporate to give it a definite shape. Depending on different modes of loco- motion and living in varying environment, the foot in Molluscs varies greatly in shape and form Variation of foot is primarily due to various physiological activities like creeping or crawling, burrowing, leaping, looping, swimming, reproduction, etc. Besides these, in parasitic and sedentary forms, the modification of foot occurs in the form of sucker, byssus apparatus, etc. Fig: Generalized Mollusc (Lateral view) Modifications of Foot 1. Foot-as the Creeping or Crawling Organ: a) Class Aplacophora: True molluscan foot is absent in Aplacophorans but some structure may be regarded to be the starting point. The ventral foot in Chaetoderma, Limifossor (Subclass Chaetodermomorpha) is absent. In Neomenia (Subclass Neomeniomorpha), a mid-ventral groove from mouth to anus with non-muscular ciliated ridge is believed to be homologous with the foot of other molluscs and serves as locomotory organ (Fig. -
Phylum Mollusca
CHAPTER 13 Phylum Mollusca olluscs include some of the best-known invertebrates; almost everyone is familiar with snails, clams, slugs, squids, and octopuses. Molluscan shells have been popular since ancient times, and some cultures still M use them as tools, containers, musical devices, money, fetishes, reli- gious symbols, ornaments, and decorations and art objects. Evidence of histori- cal use and knowledge of molluscs is seen in ancient texts and hieroglyphics, on coins, in tribal customs, and in archaeological sites and aboriginal kitchen middens or shell mounds. Royal or Tyrian purple of ancient Greece and Rome, and even Biblical blue (Num. 15:38), were molluscan pigments extracted from certain marine snails.1 Many aboriginal groups have for millenia relied on mol- luscs for a substantial portion of their diet and for use as tools. Today, coastal nations annually har- vest millions of tons of molluscs commercially for Classification of The Animal food. Kingdom (Metazoa) There are approximately 80,000 described, liv- Non-Bilateria* Lophophorata ing mollusc species and about the same number of (a.k.a. the diploblasts) PHYLUM PHORONIDA described fossil species. However, many species PHYLUM PORIFERA PHYLUM BRYOZOA still await names and descriptions, especially those PHYLUM PLACOZOA PHYLUM BRACHIOPODA from poorly studied regions and time periods, and PHYLUM CNIDARIA ECDYSOZOA it has been estimated that only about half of the liv- PHYLUM CTENOPHORA Nematoida ing molluscs have so far been described. In addi- PHYLUM NEMATODA Bilateria PHYLUM -
The Cell Lineage of the Polyplacophoran, Chaetopleura Apiculata: Variation in the Spiralian Program and Implications for Molluscan Evolution
Developmental Biology 272 (2004) 145–160 www.elsevier.com/locate/ydbio The cell lineage of the polyplacophoran, Chaetopleura apiculata: variation in the spiralian program and implications for molluscan evolution Jonathan Q. Henry,a,* Akiko Okusu,b and Mark Q. Martindalec a Department of Cell and Structural Biology, University of Illinois, Urbana, IL 61801, USA b Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA c Kewalo Marine Lab, Pacific Biomedical Research Center, University of Hawaii, Honolulu, HI 96813, USA Received for publication 27 January 2004, revised 9 April 2004, accepted 12 April 2004 Available online 7 June 2004 Abstract Polyplacophorans, or chitons, are an important group of molluscs, which are argued to have retained many plesiomorphic features of the molluscan body plan. Polyplacophoran trochophore larvae posses several features that are distinctly different from those of their sister trochozoan taxa, including modifications of the ciliated prototrochal cells, the postrochal position of the larval eyes or ocelli, epidermal calcareous spicules, and a collection of serially reiterated epidermal shell plates. Despite these differences, chitons demonstrate a canonical pattern of equal spiral cleavage shared by other spiralian phyla that permits the identification of homologous cells across this animal clade. Cell lineage analysis using intracellular labeling on one chiton species, Chaetopleura apiculata, shows that the ocelli are generated from different lineal precursors (second-quartet micromeres: 2a, 2c) compared to those in all other spiralians studied to date (first-quartet micromeres: 1a, 1c). This situation implies that significant changes have also occurred in terms of the inductive interactions that control eye development in the spiralians. -
Chapter •••••• Ten Molluscs
Hickman−Roberts−Larson: 10. Molluscs Text © The McGraw−Hill Animal Diversity, Third Companies, 2002 Edition 10 chapter •••••• ten Molluscs A Significant Space Long ago in the Precambrian era, the most complex animals populat- ing the seas were acoelomate. They must have been inefficient bur- rowers, and they were unable to exploit the rich subsurface ooze. Any that developed fluid-filled spaces within the body would have had a substantial advantage because these spaces could serve as a hydrostatic skeleton and improve burrowing efficiency. The simplest, and probably first, mode of achieving a fluid- filled space within the body was retention of the embryonic blas- tocoel, as in pseudocoelomates. This evolutionary solution was not ideal because organs lay loose in the body cavity.Improved efficiency of a pseudocoel as a hydrostatic skeleton depended on increasingly high hydrostatic pressure, a condition that severely limited the potential for adaptive radiation. Some descendants of Precambrian acoelomate organisms evolved a more elegant arrangement: a fluid-filled space within the mesoderm, the coelom. This space was lined with mesoderm, and organs were suspended by mesodermal membranes, the mesenter- ies. Not only could the coelom serve as an efficient hydrostatic skeleton, with circular and longitudinal body-wall muscles acting as antagonists, but a more stable arrangement of organs with less crowding resulted. Mesenteries provided an ideal location for networks of blood vessels, and the alimentary canal could become more muscular,more highly specialized, and more diversified with- out interfering with other organs. Development of a coelom was a major step in the evolution of larger and more complex forms. -
Monoplacophorans and the Origin and Relationships of Mollusks
Evo Edu Outreach (2009) 2:191–203 DOI 10.1007/s12052-009-0125-4 ORIGINAL SCIENTIFIC ARTICLE Monoplacophorans and the Origin and Relationships of Mollusks David R. Lindberg Published online: 15 April 2009 # The Author(s) 2009. This article is published with open access at Springerlink.com Abstract The story of the discovery and study of the Keywords Monoplacophora . Tryblidia . Mollusca . Monoplacophora (or Tryblidia) and how they have contributed Evolution . Limpet toourunderstandingoftheevolutionoftheMolluscahighlights the importance of integrating data from the fossil record with The story of the discovery of living Monoplacophora (or thestudyoflivingforms.Monoplacophorawerecommoninthe Tryblidia) and the study of both fossil and living species earlyPaleozoicandwerethoughttohavebecomeextinctduring has greatly shaped our ideas of the evolution of the the Devonian Period, approximately 375 Mya. In the mid Mollusca, and this body of work highlights the importance 1950s, they were recovered from abyssal depths off of Costa of integrating data from the fossil record with the study of Rica and were immediately heralded as a “living fossil.” The living forms. However, it also provides important examples living specimens confirmed that some of the organs (kidneys, of the caution that must be exercised when studying heart, and gills) were repeated serially, just like the shell lineages across such broad expanses of the history of life. muscles that had been observed in fossil specimens. This Monoplacophorans are one of the least known members of supported the hypothesis that they were closely related to other the living Mollusca as compared to the other groups such as segmented organisms such as annelids and arthropods. Today, Gastropoda (snails), Bivalvia (clams), and Cephalopoda there are 29 described living species and a growing body of (octopus and squids). -
Glossary of Terminology
NOAA Coral Reef Information System - Glossary of Terminology Coral Reef Information System Home Data & Publications Regional Portals CRCP Activities Glossary HOME> GLOSSARY HOME> GLOSSARY OF TERMINOLOGY AND ACRONYMS/ABBREVIATIONS Glossary of Terminology A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | abalone a univalve mollusk (class Gastropoda) of the genus Haliotis. Abalones are harvested commercially for food consumption. The shell is lined with mother- of-pearl and used for commercial (ornamental) purposes Sea otters are in direct competition with humans for abalone. (Photo: Ron McPeak) abatement reducing the degree or intensity of, or eliminating abaxial away from, or distant from the axis abbreviate shortened abdomen in higher animals, the portion of the body that contains the intestines and other http://www.coris.noaa.gov/glossary/print-glossary.html[3/10/2016 11:56:15 AM] NOAA Coral Reef Information System - Glossary of Terminology viscera other than the lungs and heart; in arthropods, the rearmost segment of the body, which contains part of the digestive tract and all the reproductive organs The ventral surface of the abdomen of an American lobster. Prominent are the swimmerettes, uropods, and telson. abdominal fin a term used to describe the location of the pelvic (ventral) fins when they are inserted far behind pectorals. This is the more primitive condition. More recently evolved conditions have the pelvic fins in the thoracic or jugular positions. A salmon, for example, has its pelvic fins in the abdominal position. An angelfish has the pelvic fins in the thoracic position, and blennies have the pelvic fins in the jugular position, anterior to the pelvic girdle abductor a type of muscle whose function is to move an appendage or body part away from the body of an animal. -
Deep-Sea Video Technology Tracks a Monoplacophoran to the End of Its Trail (Mollusca, Tryblidia)
Marine Biodiversity https://doi.org/10.1007/s12526-018-0860-2 ORIGINAL PAPER Deep-sea video technology tracks a monoplacophoran to the end of its trail (Mollusca, Tryblidia) Julia D. Sigwart1,2 & Mary K. Wicksten3 & Matthew G. Jackson4 & Santiago Herrera5 Received: 20 September 2017 /Revised: 29 January 2018 /Accepted: 20 February 2018 # The Author(s) 2018. This article is an open access publication Abstract Originally known as fossils from the Cambrian to the Devonian, the finding of a living monoplacophoran mollusc in 1952 was one of the great zoological discoveries of the twentieth century. Now, over 35 living species have been documented from deep- sea locations around the world, mainly from samples collected with trawls. Encountering these animals is extremely rare, and in situ observations are scant. Here, we report two new sightings and ecological data for a probable undescribed species of Neopilina including the first ever high-definition close-up video of these monoplacophorans in their natural environment, obtained while exploring seamount environments in American Samoa. Extensive trackways, similar to those associated with the monoplacophoran siting, may be evidence of a larger population at both seamounts. Living monoplacophorans are important to understanding the recent evolution of deep-sea fauna, yet their habitat, on polymetallic nodules and ferromanganese crusts, is under rapidly increasing pressure for deep-sea mineral extraction. Keywords Molluscan evolution . Monoplacophora . trackways . ROV . Deep sea . marine conservation Introduction distinct taxonomic class, separate from all other molluscs. Unlike gastropods, the animals have no eyes or head per se, When a living monoplacophoran was recognised in 1952 their body musculature is anchored to a conical shell by eight (Lemche 1957), it was hailed as one of the great zoological pairs of dorso-ventral muscles, and they have gills on both discoveries of the twentieth century (Lindberg 2009).