Bivalve Biology - Glossary
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Marine Bivalve Molluscs
Marine Bivalve Molluscs Marine Bivalve Molluscs Second Edition Elizabeth Gosling This edition first published 2015 © 2015 by John Wiley & Sons, Ltd First edition published 2003 © Fishing News Books, a division of Blackwell Publishing Registered Office John Wiley & Sons, Ltd, The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK Editorial Offices 9600 Garsington Road, Oxford, OX4 2DQ, UK The Atrium, Southern Gate, Chichester, West Sussex, PO19 8SQ, UK 111 River Street, Hoboken, NJ 07030‐5774, USA For details of our global editorial offices, for customer services and for information about how to apply for permission to reuse the copyright material in this book please see our website at www.wiley.com/wiley‐blackwell. The right of the author to be identified as the author of this work has been asserted in accordance with the UK Copyright, Designs and Patents Act 1988. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, except as permitted by the UK Copyright, Designs and Patents Act 1988, without the prior permission of the publisher. Designations used by companies to distinguish their products are often claimed as trademarks. All brand names and product names used in this book are trade names, service marks, trademarks or registered trademarks of their respective owners. The publisher is not associated with any product or vendor mentioned in this book. Limit of Liability/Disclaimer of Warranty: While the publisher and author(s) have used their best efforts in preparing this book, they make no representations or warranties with respect to the accuracy or completeness of the contents of this book and specifically disclaim any implied warranties of merchantability or fitness for a particular purpose. -
Occurence of Pisidium Conventus Aff. Akkesiense in Gunma Prefecture
VENUS 62 (3-4): 111-116, 2003 Occurence Occurence of Pisidium conventus aff.α kkesiense in Gunma Prefecture, Japan (Bivalvia: Sphaeriidae) Hiroshi Hiroshi Ieyama1 and Shigeru Takahashi2 Faculty 1Faculty of Education, Ehime Universi η,Bun わ1ocho 3, 2 3, Ehime 790-857 スJapan; [email protected] Yakura Yakura 503-2, Agatsuma-cho, Gunma 377 同 0816, Japan Abstract: Abstract: Shell morphology and 姐 atomy of Pisidium conventus aff. akkesiense collect 巴d from from a fish-culture pond were studied. This species showed similarities to the subgenus Neopisidium Neopisidium with respect to ligament position and gill, res 巴mbling P. conventus in anatomical characters. characters. Keywords: Keywords: Pisidium, Sphaeriidae, gill, mantle, brood pouch Introduction Introduction Komiushin (1999) demonstrated that anatomical features are useful for species diagnostics 佃 d classification of Pisidium, including the demibranchs, siphons, mantle edge and musculature, brood brood pouch, and nephridium. These taxonomical characters are still poorly known in Japanese species species of Pisidium. An anatomical study of P. casertanum 仕om Lake Biwa (Komiushin, 1996) was 祖巴arly report. Onoyama et al. (2001) described differences in the arrangement of gonadal tissues tissues in P. parvum and P. casertanum. Mori (1938) classified Japanese Pisidium into 24 species and subspecies based on minor differences differences in shell characters. For a critical revision of Japanese Pisidium, it is important to study as as many species as possible from various locations in and around Japan. This study includes details details of shell and soft p 紅 t mo 中hology of Pisidium conventus aff. akkesiense from Gunma Prefecture Prefecture in central Honshu. -
In Bahia, Brazil
Volume 52(40):515‑524, 2012 A NEW GENUS AND SPECIES OF CAVERNICOLOUS POMATIOPSIDAE (MOLLUSCA, CAENOGASTROPODA) IN BAHIA, BRAZIL 1 LUIZ RICARDO L. SIMONE ABSTRACT Spiripockia punctata is a new genus and species of Pomatiopsidae found in a cave from Serra Ramalho, SW Bahia, Brazil. The taxon is troglobiont (restricted to subterranean realm), and is characterized by the shell weakly elongated, fragile, translucent, normally sculptured by pus‑ tules with periostracum hair on tip of pustules; peristome highly expanded; umbilicus opened; radular rachidian with 6 apical and 3 pairs of lateral cusps; osphradium short, arched; gill filaments with rounded tip; prostate flattened, with vas deferens inserting subterminally; penis duct narrow and weakly sinuous; pallial oviduct simple anteriorly, possessing convoluted by‑ pass connecting base of bulged portion of transition between visceral and pallial oviducts with base of seminal receptacle; spermathecal duct complete, originated from albumen gland. The description of this endemic species may raise protective environmental actions to that cave and to the Serra Ramalho Karst area. Key-Words: Pomatiopsidae; Spiripockia punctata gen. nov. et sp. nov.; Brazil; Cave; Tro- globiont; Anatomy. INTRODUCTION An enigmatic tiny gastropod has been collected in caves from the Serra Ramalho Kars area, southwestern The family Pomatiopsidae is represented in the Bahia state, Brazil. It has a pretty, fragile, translucent Brazilian region by only two species of the genus Id‑ shell in such preliminary gross anatomy, which already iopyrgus Pilsbry, 1911 (Simone, 2006: 94). However, reveals troglobiont adaptations, i.e., depigmentation, the taxon is much richer in remaining mainland ar- lack of eyes and small size. The sample has been brought eas, with both freshwater and semi-terrestrial habits by Maria Elina Bichuette, who is specialized in subter- (Ponder & Keyzer, 1998; Kameda & Kato, 2011). -
(Gastropoda: Cocculiniformia) from Off the Caribbean Coast of Colombia
ó^S PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON ll8(2):344-366. 2005. Cocculinid and pseudococculinid limpets (Gastropoda: Cocculiniformia) from off the Caribbean coast of Colombia Néstor E. Ardila and M. G. Harasewych (NEA) Museo de Historia Natural Marina de Colombia, Instituto de Investigaciones Marinas, INVEMAR, Santa Marta, A.A. 1016, Colombia, e-mail: [email protected]; (MGH) Department of Invertebrate Zoology, MRC-I63, National Museum of Natural History, Smithsonian Institution, Washington, D.C. 20013-7012 U.S.A., e-mail: [email protected] Abstract.•The present paper reports on the occurrence of six species of Cocculinidae and three species of Pseudococculinidae off the Caribbean coast of Colombia. Cocculina messingi McLean & Harasewych, 1995, Cocculina emsoni McLean & Harasewych, 1995 Notocrater houbricki McLean & Hara- sewych, 1995 and Notocrater youngi McLean & Harasewych, 1995 were not previously known to occur within the of the Caribbean Sea, while Fedikovella beanii (Dall, 1882) had been reported only from the western margins of the Atlantic Ocean, including the lesser Antilles. New data are presented on the external anatomy and radular morphology of Coccocrater portoricensis (Dall & Simpson, 1901) that supports its placement in the genus Coccocrater. Coc- culina fenestrata n. sp. (Cocculinidae) and Copulabyssia Colombia n. sp. (Pseu- dococculinidae) are described from the upper continental slope of Caribbean Colombia. Cocculiniform limpets comprise two paraphyletic, with the Cocculinoidea related groups of bathyal to hadal gastropods with to Neomphalina and the Lepetelloidea in- global distribution that live primarily on cluded within Vetigastropoda (Ponder & biogenic substrates (e.g., wood, algal hold- Lindberg 1996, 1997; McArthur & Hara- fasts, whale bone, cephalopod beaks, crab sewych 2003). -
Light Exposure Enhances Urea Absorption in the Fluted Giant Clam
© 2018. Published by The Company of Biologists Ltd | Journal of Experimental Biology (2018) 221, jeb176313. doi:10.1242/jeb.176313 RESEARCH ARTICLE Light exposure enhances urea absorption in the fluted giant clam, Tridacna squamosa, and up-regulates the protein abundance of a light-dependent urea active transporter, DUR3-like, in its ctenidium Christabel Y. L. Chan1, Kum C. Hiong1, Mel V. Boo1, Celine Y. L. Choo1, Wai P. Wong1, Shit F. Chew2 and Yuen K. Ip1,3,* ABSTRACT Symbiodinium, which are also known as zooxanthellae (Trench, Giant clams live in nutrient-poor reef waters of the Indo-Pacific and rely 1987). Giant clams (Phylum: Mollusca, Family: Cardiidae, on symbiotic dinoflagellates (Symbiodinium spp., also known as Subfamily: Tridacninae, Genus: Tridacna or Hippopus)are zooxanthellae) for nutrients. As the symbionts are nitrogen deficient, common inhabitants of coral reefs in the tropical Indo-Pacific. the host clam has to absorb exogenous nitrogen and supply it to them. The host clam harbors symbiotic zooxanthellae (Symbiodinium This study aimed to demonstrate light-enhanced urea absorption in the clade A, C and D; LaJuenesse et al., 2004; Takabayashi et al., 2004; fluted giant clam, Tridacna squamosa, and to clone and characterize Hernawan, 2008; Lee et al., 2015) which live extracellularly in a the urea active transporter DUR3-like from its ctenidium (gill). The branched tubular system surrounded by hemolymph (Norton et al., results indicate that T. squamosa absorbs exogenous urea, and the 1992). Zooxanthellae reside mainly inside the tiny tertiary tubules rate of urea uptake in the light was significantly higher than that in located below the surface of the fleshy and colorful outer mantle darkness. -
Freshwater Mussels of the Pacific Northwest
Freshwater Mussels of the Pacifi c Northwest Ethan Nedeau, Allan K. Smith, and Jen Stone Freshwater Mussels of the Pacifi c Northwest CONTENTS Part One: Introduction to Mussels..................1 What Are Freshwater Mussels?...................2 Life History..............................................3 Habitat..................................................5 Role in Ecosystems....................................6 Diversity and Distribution............................9 Conservation and Management................11 Searching for Mussels.............................13 Part Two: Field Guide................................15 Key Terms.............................................16 Identifi cation Key....................................17 Floaters: Genus Anodonta.......................19 California Floater...................................24 Winged Floater.....................................26 Oregon Floater......................................28 Western Floater.....................................30 Yukon Floater........................................32 Western Pearlshell.................................34 Western Ridged Mussel..........................38 Introduced Bivalves................................41 Selected Readings.................................43 www.watertenders.org AUTHORS Ethan Nedeau, biodrawversity, www.biodrawversity.com Allan K. Smith, Pacifi c Northwest Native Freshwater Mussel Workgroup Jen Stone, U.S. Fish and Wildlife Service, Columbia River Fisheries Program Offi ce, Vancouver, WA ACKNOWLEDGEMENTS Illustrations, -
The Pax Gene Family: Highlights from Cephalopods Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, Yann Bassaglia
The Pax gene family: Highlights from cephalopods Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, Yann Bassaglia To cite this version: Sandra Navet, Auxane Buresi, Sébastien Baratte, Aude Andouche, Laure Bonnaud-Ponticelli, et al.. The Pax gene family: Highlights from cephalopods. PLoS ONE, Public Library of Science, 2017, 12 (3), pp.e0172719. 10.1371/journal.pone.0172719. hal-01921138 HAL Id: hal-01921138 https://hal.archives-ouvertes.fr/hal-01921138 Submitted on 13 Nov 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License RESEARCH ARTICLE The Pax gene family: Highlights from cephalopods Sandra Navet1☯, Auxane Buresi1☯, SeÂbastien Baratte1,2, Aude Andouche1, Laure Bonnaud-Ponticelli1, Yann Bassaglia1,3* 1 UMR BOREA MNHN/CNRS7208/IRD207/UPMC/UCN/UA, MuseÂum National d'Histoire Naturelle, Sorbonne UniversiteÂs, Paris, France, 2 Univ. Paris Sorbonne-ESPE, Sorbonne UniversiteÂs, Paris, France, 3 Univ. Paris Est CreÂteil-Val de Marne, CreÂteil, France ☯ These authors contributed equally to this work. * [email protected] a1111111111 a1111111111 a1111111111 a1111111111 Abstract a1111111111 Pax genes play important roles in Metazoan development. Their evolution has been exten- sively studied but Lophotrochozoa are usually omitted. -
Key to the Freshwater Bivalves of New Jersey
Key to the Freshwater Bivalves of New Jersey 1. a. shell with a very sharp posterior ridge, shaped like the marine mussel, Mytilus, generally less than 30 mm, and attached to a hard substrate with byssal threads.........................……………........................Zebra mussel b. animal without byssal threads attaching adult to substrate, with or without teeth but not with the above shape................................….............................2 2. a. valves with cardinal teeth and two sets of lateral teeth.......................…...............................3 b. valves with one set of lateral teeth and pseudocardinal teeth or without teeth.............................................................................................................5 3. a. shell thick and sturdy, beak bulbous and curving anteriorly………………….Atlantic rangia b. shell moderately thick, beak not bulbous nor curving…………………………………………...4 4. a. valves with serrated lateral teeth......................................……….........................Asian clam b. valves with smooth lateral teeth....................................................................Fingernail clam 5. a. hinge teeth absent.................................................................................................................6 b. hinge teeth present..............................................................................................................10 6. a. beaks not projecting above the hinge line................…………………........ Paper pondshell b. beaks projecting above -
Transposed Hinge Structures in Lamellibranches
TRANSACTIONS OF THE • SAN DIEGO SOCIETY OF NATURAL HISTORY ,/ VoLUME VII, No. 26, pp. 299-318, plate 19 • TRANSPOSED HINGE STRUCTURES IN LAMELLIBRANCHS BY P. PoPENOE AND FINDLAY W. W. A. • Balch Graduate School of the Geological Sciences California Institute of Technology Pasadena, California SAN DIEGO, CALIFORNIA PRINTED FOR THE SOCIETY OCTOBER 6, 1933 • • COMMITTEE ON PUBLICATION U.S. GRANT, IV, Chairman FRED BAKER CLINTON G. ABBOTT, Editor • TRANSPOSED HINGE STRUCTURES IN LAMELLIBRANCHS 1 BY W. P. PoPENOE AND W. A. FINDLAY California Institute of Technology INTRODUCTION In the course of study of a collection of Eocene fossils from Claiborne Bluff, Alabama, the senior author of tl1is paper noticed two valves, one right and one left, of the lamellibranch Venericardia parva Lea, in whicl1 the dentition is partially transposed. Subsequently, the authors made an examination of more than five thousand lamellibranch valves, representit1g both recent and fossil shells, in search of further exa1nples of hinge-trans position. We have found a total number of twenty-six valves exhibiting this variation. Study of these specimens has revealed some hitherto unreported facts regarding the principles of hinge-transposition. Therefore in this paper, we shall describe and discuss these specimens, and shall present such con clusions as seem justified by the data assembled. Citations to the literature are made by author, date, and page, referring to the list at the end of the paper. DEFINITION OF T ERMS A transposed lamellibranch hinge is defined as one that exhibits in the right valve the hinge ele1nents normally occurring in the left valve, and vice-versa. -
Interpreting Amphioxus, and Thoughts on Ancestral Chordate Mouths and Brains THURSTON LACALLI*
Int. J. Dev. Biol. 61: 649-654 (2017) doi: 10.1387/ijdb.170105tl www.intjdevbiol.com Interpreting amphioxus, and thoughts on ancestral chordate mouths and brains THURSTON LACALLI* Biology Department, University of Victoria, Victoria, Canada ABSTRACT Amphioxus is increasingly important as a model for ancestral chordates. Nevertheless, it is secondarily modified in various ways, especially in the larva, whose small size has resulted in a rescaling and repositioning of structures. This is especially pronounced in the head region, where the mouth opens asymmetrically on the left side, leading to speculation that the mouth is sec- ondarily derived, e.g. from a gill slit, and is hence not homologous with mouths in other animals. The available evidence does not, in the author’s view, support this interpretation. A second issue is raised concerning the identity and function of the midbrain homolog, whose extent depends on whether greater weight is given to dorsal landmarks in the nerve cord or ventral ones. The presence of two sets of dorsal photoreceptors, the lamellar body and Joseph cells, functionally links the region they occupy to the vertebrate midbrain. The midbrain is currently suggested to be the brain region in which primary consciousness emerged during early vertebrate evolution, so the origin of its constituent cells is of special interest. Possible amphioxus homologs include the anterior-most group of dorsal bipolar cells (ADBs), which are apico-basally inverted (i.e. synapse-bearing neurites arise from the apical cell compartment) in the same fashion as cortical neurons in vertebrates. This may have been a crucial innovation for chordates, responsible for both improved sensory process- ing and, eventually, consciousness. -
Copyrighted Material
319 Index a oral cavity 195 guanocytes 228, 231, 233 accessory sex glands 125, 316 parasites 210–11 heart 235 acidophils 209, 254 pharynx 195, 197 hemocytes 236 acinar glands 304 podocytes 203–4 hemolymph 234–5, 236 acontia 68 pseudohearts 206, 208 immune system 236 air sacs 305 reproductive system 186, 214–17 life expectancy 222 alimentary canal see digestive setae 191–2 Malpighian tubules 232, 233 system taxonomy 185 musculoskeletal system amoebocytes testis 214 226–9 Cnidaria 70, 77 typhlosole 203 nephrocytes 233 Porifera 28 antennae nervous system 237–8 ampullae 10 Decapoda 278 ocelli 240 Annelida 185–218 Insecta 301, 315 oral cavity 230 blood vessels 206–8 Myriapoda 264, 275 ovary 238 body wall 189–94 aphodus 38 pedipalps 222–3 calciferous glands 197–200 apodemes 285 pharynx 230 ciliated funnel 204–5 apophallation 87–8 reproductive system 238–40 circulatory system 205–8 apopylar cell 26 respiratory system 236–7 clitellum 192–4 apopyle 38 silk glands 226, 242–3 coelomocytes 208–10 aquiferous system 21–2, 33–8 stercoral sac 231 crop 200–1 Arachnida 221–43 sucking stomach 230 cuticle 189 biomedical applications 222 taxonomy 221 diet 186–7 body wall 226–9 testis 239–40 digestive system 194–203 book lungs 236–7 tracheal tube system 237 dissection 187–9 brain 237 traded species 222 epidermis 189–91 chelicera 222, 229 venom gland 241–2 esophagus 197–200 circulatory system 234–6 walking legs 223 excretory system 203–5 COPYRIGHTEDconnective tissue 228–9 MATERIALzoonosis 222 ganglia 211–13 coxal glands 232, 233–4 archaeocytes 28–9 giant nerve -
Exputens) in Mexico, and a Review of All Species of This North American Subgenus
Natural History Museum /U, JH caY-^A 19*90 la Of Los Angeles County THE VELIGER © CMS, Inc., 1990 The Veliger 33(3):305-316 (July 2, 1990) First Occurrence of the Tethyan Bivalve Nayadina (.Exputens) in Mexico, and a Review of All Species of This North American Subgenus by RICHARD L. SQUIRES Department of Geological Sciences, California State University, Northridge, California 91330, USA Abstract. The malleid bivalve Nayadina (Exputens) has Old World Tethyan affinities but is known only from Eocene deposits in North America. Nayadina (Exputens) is reported for the first time from Mexico. About 50 specimens of N. (E.) batequensis sp. nov. were found in warm-water nearshore deposits of the middle lower Eocene part of the Bateque Formation, just south of Laguna San Ignacio, on the Pacific coast of Baja California Sur. The new species shows a wide range of morphologic variability especially where the beaks and auricles are located and how much they are developed. A review of the other species of Exputens, namely Nayadina (E.) llajasensis (Clark, 1934) from California and N. (E.) ocalensis (MacNeil, 1934) from Florida, Georgia, and North Carolina, revealed that they also have a wide range of morphologic variability. Nayadina (E.) alexi (Clark, 1934) is shown, herein, to be a junior synonym of N. (E.) llajasensis. The presence of a byssal sinus is recognized for the first time in Exputens. An epifaunal nestling mode of life, with attachment by byssus to hard substrate, can now be assumed for Exputens. INTRODUCTION species. It became necessary to thoroughly examine them, The macropaleontology of Eocene marine deposits in Baja and after such a study, it was found that the Bateque California Sur, Mexico, is largely an untouched subject.