Phylum: Annelida
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Phylogenetic Relationships of Serpulidae (Annelida: Polychaeta) Based on 18S Rdna Sequence Data, and Implications for Opercular Evolution Janina Lehrkea,Ã, Harry A
ARTICLE IN PRESS Organisms, Diversity & Evolution 7 (2007) 195–206 www.elsevier.de/ode Phylogenetic relationships of Serpulidae (Annelida: Polychaeta) based on 18S rDNA sequence data, and implications for opercular evolution Janina Lehrkea,Ã, Harry A. ten Hoveb, Tara A. Macdonaldc, Thomas Bartolomaeusa, Christoph Bleidorna,1 aInstitute for Zoology, Animal Systematics and Evolution, Freie Universitaet Berlin, Koenigin-Luise-Street 1-3, 14195 Berlin, Germany bZoological Museum, University of Amsterdam, P.O. Box 94766, 1090 GT Amsterdam, The Netherlands cBamfield Marine Sciences Centre, Bamfield, British Columbia, Canada, V0R 1B0 Received 19 December 2005; accepted 2 June 2006 Abstract Phylogenetic relationships of (19) serpulid taxa (including Spirorbinae) were reconstructed based on 18S rRNA gene sequence data. Maximum likelihood, Bayesian inference, and maximum parsimony methods were used in phylogenetic reconstruction. Regardless of the method used, monophyly of Serpulidae is confirmed and four monophyletic, well- supported major clades are recovered: the Spirorbinae and three groups hitherto referred to as the Protula-, Serpula-, and Pomatoceros-group. Contrary to the taxonomic literature and the hypothesis of opercular evolution, the Protula- clade contains non-operculate (Protula, Salmacina) and operculate taxa both with pinnulate and non-pinnulate peduncle (Filograna vs. Vermiliopsis), and most likely is the sister group to Spirorbinae. Operculate Serpulinae and poorly or non-operculate Filograninae are paraphyletic. It is likely that lack of opercula in some serpulid genera is not a plesiomorphic character state, but reflects a special adaptation. r 2007 Gesellschaft fu¨r Biologische Systematik. Published by Elsevier GmbH. All rights reserved. Keywords: Serpulidae; Phylogeny; Operculum; 18S rRNA gene; Annelida; Polychaeta Introduction distinctive calcareous tubes and bilobed tentacular crowns, each with numerous radioles that bear shorter Serpulids are common members of marine hard- secondary branches (pinnules) on the inner side. -
DEEP SEA LEBANON RESULTS of the 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project
DEEP SEA LEBANON RESULTS OF THE 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project March 2018 DEEP SEA LEBANON RESULTS OF THE 2016 EXPEDITION EXPLORING SUBMARINE CANYONS Towards Deep-Sea Conservation in Lebanon Project Citation: Aguilar, R., García, S., Perry, A.L., Alvarez, H., Blanco, J., Bitar, G. 2018. 2016 Deep-sea Lebanon Expedition: Exploring Submarine Canyons. Oceana, Madrid. 94 p. DOI: 10.31230/osf.io/34cb9 Based on an official request from Lebanon’s Ministry of Environment back in 2013, Oceana has planned and carried out an expedition to survey Lebanese deep-sea canyons and escarpments. Cover: Cerianthus membranaceus © OCEANA All photos are © OCEANA Index 06 Introduction 11 Methods 16 Results 44 Areas 12 Rov surveys 16 Habitat types 44 Tarablus/Batroun 14 Infaunal surveys 16 Coralligenous habitat 44 Jounieh 14 Oceanographic and rhodolith/maërl 45 St. George beds measurements 46 Beirut 19 Sandy bottoms 15 Data analyses 46 Sayniq 15 Collaborations 20 Sandy-muddy bottoms 20 Rocky bottoms 22 Canyon heads 22 Bathyal muds 24 Species 27 Fishes 29 Crustaceans 30 Echinoderms 31 Cnidarians 36 Sponges 38 Molluscs 40 Bryozoans 40 Brachiopods 42 Tunicates 42 Annelids 42 Foraminifera 42 Algae | Deep sea Lebanon OCEANA 47 Human 50 Discussion and 68 Annex 1 85 Annex 2 impacts conclusions 68 Table A1. List of 85 Methodology for 47 Marine litter 51 Main expedition species identified assesing relative 49 Fisheries findings 84 Table A2. List conservation interest of 49 Other observations 52 Key community of threatened types and their species identified survey areas ecological importanc 84 Figure A1. -
From the Barremian (Lower Cretaceous) of the Serre De Bleyton (Drôme, SE France)
Ann. Naturhist. Mus. Wien, Serie A 113 675–733 Wien, Mai 2011 Sabellidae, Serpulidae and Spirorbinae (Polychaeta sedentaria) from the Barremian (Lower Cretaceous) of the Serre de Bleyton (Drôme, SE France) By Manfred JÄGER (With 10 plates and 1 figure) Manuscript submitted on October 18th 2010, the revised manuscript on February 9th 2011 Abstract The Barremian of the Serre de Bleyton has yielded many calcareous tubes and tube fragments of a diverse polychaete fauna of circa 20 species, many of them new to science. One new genus, Pseudomicrorbis nov. gen., and seven new species are introduced, Metavermilia (Vepreculina) infracretacea nov. spec., Filogranula? provencalis nov. spec., Mucroserpula pentaditrupoidea nov. spec., Mucroserpula? bleytonensis nov. spec., Pyrgopolon (Pyrgopolon?) moosleitneri nov. spec., Pseudomicrorbis pseudomicrorbis nov. spec. and Neomicrorbis barremiensis nov. spec. Compared to the Upper Jurassic and especially the Upper Cretaceous, the Lower Cretaceous sabel- lid and serpulid fauna has so far received comparatively little attention. This Barremian fauna fills a stratigraphical gap from which only few sabellids and serpulids had been described so far. The high percentage of new species is due to the fact that most of the Lower Cretaceous sabellid and serpulid faunas described till now are found in the boreal realm, thus explaining the outstanding high diversity of the Tethyal Serre de Bleyton fauna compared to that of Germany and England. The high diverse fauna includes both surprisingly modern elements as well as “old-fashioned” forms resembling Jurassic species. On the one hand, one of the geologically earliest representatives of Pyrgopolon and a relatively diverse fauna of small spirorbins were found here. -
Annelida, Amphinomidae) in the Mediterranean Sea with an Updated Revision of the Alien Mediterranean Amphinomids
A peer-reviewed open-access journal ZooKeys 337: 19–33 (2013)On the occurrence of the firewormEurythoe complanata complex... 19 doi: 10.3897/zookeys.337.5811 RESEARCH ARTICLE www.zookeys.org Launched to accelerate biodiversity research On the occurrence of the fireworm Eurythoe complanata complex (Annelida, Amphinomidae) in the Mediterranean Sea with an updated revision of the alien Mediterranean amphinomids Andrés Arias1, Rômulo Barroso2,3, Nuria Anadón1, Paulo C. Paiva4 1 Departamento de Biología de Organismos y Sistemas (Zoología), Universidad de Oviedo, Oviedo 33071, Spain 2 Pontifícia Universidade Católica do Rio de Janeiro , Rio de Janeiro, Brazil 3 Museu de Zoologia da Unicamp, Campinas, SP, Brazil 4 Departamento de Zoologia, Instituto de Biologia, Universidade Federal do Rio de Janeiro (UFRJ) , Rio de Janeiro, RJ, Brasil Corresponding author: Andrés Arias ([email protected]) Academic editor: C. Glasby | Received 17 June 2013 | Accepted 19 September 2013 | Published 30 September 2013 Citation: Arias A, Barroso R, Anadón N, Paiva PC (2013) On the occurrence of the fireworm Eurythoe complanata complex (Annelida, Amphinomidae) in the Mediterranean Sea with an updated revision of the alien Mediterranean amphinomids. ZooKeys 337: 19–33. doi: 10.3897/zookeys.337.5811 Abstract The presence of two species within the Eurythoe complanata complex in the Mediterranean Sea is reported, as well as their geographical distributions. One species, Eurythoe laevisetis, occurs in the eastern and cen- tral Mediterranean, likely constituting the first historical introduction to the Mediterranean Sea and the other, Eurythoe complanata, in both eastern and Levantine basins. Brief notes on their taxonomy are also provided and their potential pathways for introduction to the Mediterranean are discussed. -
Eunicida and Amphinomida Polychaetes (Annelida) Inhabiting Dead Coral Fragments in the Chinchorro Bank Biosphere Reserve, Mexican Caribbean
Eunicida and Amphinomida polychaetes (Annelida) inhabiting dead coral fragments in the Chinchorro Bank Biosphere Reserve, Mexican Caribbean Pablo Hernández-Alcántara1, Ismael Narciso Cruz-Pérez2 & Vivianne Solís-Weiss3 1. Unidad Académica de Ecología y Biodiversidad Acuática, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México. Circuito Exterior S/N, Cd. Universitaria, Ciudad de México, 04510, México, [email protected] 2. Facultad de Estudios Superiores Zaragoza, Universidad Nacional Autónoma de México. Batalla 5 de mayo S/N esquina Fuerte de Loreto, Colonia Ejército de Oriente, C.P. 09230, Ciudad de México, México, [email protected] 3. Unidad Académica de Sistemas Arrecifales, Instituto de Ciencias del Mar y Limnología, Universidad Nacional Autónoma de México. Prol. Av. Niños Héroes s/n Puerto Morelos Quintana Roo, 77580, México, [email protected] Received 08-VII-2018. Corrected 20-V-2019. Accepted 30-VI-2019. ABSTRACT. Introduction: The polychaete fauna inhabiting Chinchorro Bank has been poorly studied and only 35 species have been previously reported. Objective: To examine the taxonomic composition of the Eunicida and Amphinomida associated to dead coral substrates from this coral reef atoll, a Biosphere Reserve located in the southern Mexican Caribbean. Methods: In April 2008, dead coral fragments of the genus Porites were manually collected by SCUBA diving at eight stations between 4-16.2 m depth. Results: A total of 714 individuals belonging to 17 genera and 48 species of the families Amphinomidae, Dorvilleidae, Eunicidae, Lumbrineridae, Oenonidae and Onuphidae were identified. Eunicidae was clearly the more diverse (29 species; 60.4 %) and abundant family (479 individuals; 67.1 %), while the Oenonidae and Onuphidae were represented by only one individual-species each. -
Download Full Article 2.4MB .Pdf File
Memoirs of Museum Victoria 71: 217–236 (2014) Published December 2014 ISSN 1447-2546 (Print) 1447-2554 (On-line) http://museumvictoria.com.au/about/books-and-journals/journals/memoirs-of-museum-victoria/ Original specimens and type localities of early described polychaete species (Annelida) from Norway, with particular attention to species described by O.F. Müller and M. Sars EIVIND OUG1,* (http://zoobank.org/urn:lsid:zoobank.org:author:EF42540F-7A9E-486F-96B7-FCE9F94DC54A), TORKILD BAKKEN2 (http://zoobank.org/urn:lsid:zoobank.org:author:FA79392C-048E-4421-BFF8-71A7D58A54C7) AND JON ANDERS KONGSRUD3 (http://zoobank.org/urn:lsid:zoobank.org:author:4AF3F49E-9406-4387-B282-73FA5982029E) 1 Norwegian Institute for Water Research, Region South, Jon Lilletuns vei 3, NO-4879 Grimstad, Norway ([email protected]) 2 Norwegian University of Science and Technology, University Museum, NO-7491 Trondheim, Norway ([email protected]) 3 University Museum of Bergen, University of Bergen, PO Box 7800, NO-5020 Bergen, Norway ([email protected]) * To whom correspondence and reprint requests should be addressed. E-mail: [email protected] Abstract Oug, E., Bakken, T. and Kongsrud, J.A. 2014. Original specimens and type localities of early described polychaete species (Annelida) from Norway, with particular attention to species described by O.F. Müller and M. Sars. Memoirs of Museum Victoria 71: 217–236. Early descriptions of species from Norwegian waters are reviewed, with a focus on the basic requirements for re- assessing their characteristics, in particular, by clarifying the status of the original material and locating sampling sites. A large number of polychaete species from the North Atlantic were described in the early period of zoological studies in the 18th and 19th centuries. -
Neanthes Limnicola Class: Polychaeta, Errantia
Phylum: Annelida Neanthes limnicola Class: Polychaeta, Errantia Order: Phyllodocida, Nereidiformia A mussel worm Family: Nereididae, Nereidinae Taxonomy: Depending on the author, Ne- wider than long, with a longitudinal depression anthes is currently considered a separate or (Fig. 2b). subspecies to the genus Nereis (Hilbig Trunk: Very thick segments that are 1997). Nereis sensu stricto differs from the wider than they are long, gently tapers to pos- genus Neanthes because the latter genus terior (Fig. 1). includes species with spinigerous notosetae Posterior: Pygidium bears two, styli- only. Furthermore, N. limnicola has most form ventrolateral anal cirri that are as long as recently been included in the genus (or sub- last seven segments (Fig. 1) (Hartman 1938). genus) Hediste due to the neuropodial setal Parapodia: The first two setigers are unira- morphology (Sato 1999; Bakken and Wilson mous. All other parapodia are biramous 2005; Tusuji and Sato 2012). However, re- (Nereididae, Blake and Ruff 2007) where both production is markedly different in N. limni- notopodia and neuropodia have acicular lobes cola than other Hediste species (Sato 1999). and each lobe bears 1–3 additional, medial Thus, synonyms of Neanthes limnicola in- and triangular lobes (above and below), called clude Nereis limnicola (which was synony- ligules (Blake and Ruff 2007) (Figs. 1, 5). The mized with Neanthes lighti in 1959 (Smith)), notopodial ligule is always smaller than the Nereis (Neanthes) limnicola, Nereis neuropodial one. The parapodial lobes are (Hediste) limnicola and Hediste limnicola. conical and not leaf-like or globular as in the The predominating name in current local in- family Phyllodocidae. (A parapodium should tertidal guides (e.g. -
H1.1 Open Water
PAGE .............................................................. 392 ▼ H1.1 OPEN WATER The open-water offshore habitat covers an area of by which solar energy enters the marine ecosystem, Nova Scotia larger than the land mass, and includes similar to the layer of plants on land. The ocean H1.1 Open Water salt water in inlets, bays and estuaries. The water waters are distinctive in having fostered the origins and the organisms it supports are the primary means of life on the planet. Plate H1.1.1: Right Whale, north of Brier Island (Unit 912). Photo: BIOS Habitats Natural History of Nova Scotia, Volume I © Nova Scotia Museum of Natural History .............................................................. PAGE 393 ▼ FORMATION PLANTS Oceans are formed as part of major geological events. The plants of the open ocean are almost entirely Nova Scotia’s open-ocean habitats are part of the microscopic algae, collectively known as phyto- Atlantic Ocean, which opened during the Jurassic plankton. Many different species occur, including Period and has been in continuous existence ever representatives of the prochlorophytes (blue-green since. The quality and depth of the water column algae—evolutionary intermediates between bacteria have fluctuated in relation to post-glacial climatic and algae), diatoms, dinoflagellates, chrysomonads, conditions. cryptomonads, minute flagellates and unicellular reproductive stages of macroscopic algae. Phyto- H1.1 PHYSICAL ASPECTS plankton are often grouped in size classes: Open Water 1. Water conditions, such as salinity, temperature, macroplankton: 200–2000 micrometres, includes ice-formation, turbidity, light penetration, tides larger diatoms. and currents, are extremely variable in the microplankton: 20–200 micrometres, includes waters offshore. most diatoms. 2. Air-water interaction, surface-water turbulence nanoplankton: 2–20 micrometres, includes determines the level of wave and gas exchange. -
OREGON ESTUARINE INVERTEBRATES an Illustrated Guide to the Common and Important Invertebrate Animals
OREGON ESTUARINE INVERTEBRATES An Illustrated Guide to the Common and Important Invertebrate Animals By Paul Rudy, Jr. Lynn Hay Rudy Oregon Institute of Marine Biology University of Oregon Charleston, Oregon 97420 Contract No. 79-111 Project Officer Jay F. Watson U.S. Fish and Wildlife Service 500 N.E. Multnomah Street Portland, Oregon 97232 Performed for National Coastal Ecosystems Team Office of Biological Services Fish and Wildlife Service U.S. Department of Interior Washington, D.C. 20240 Table of Contents Introduction CNIDARIA Hydrozoa Aequorea aequorea ................................................................ 6 Obelia longissima .................................................................. 8 Polyorchis penicillatus 10 Tubularia crocea ................................................................. 12 Anthozoa Anthopleura artemisia ................................. 14 Anthopleura elegantissima .................................................. 16 Haliplanella luciae .................................................................. 18 Nematostella vectensis ......................................................... 20 Metridium senile .................................................................... 22 NEMERTEA Amphiporus imparispinosus ................................................ 24 Carinoma mutabilis ................................................................ 26 Cerebratulus californiensis .................................................. 28 Lineus ruber ......................................................................... -
(Polychaeta) Borings in Paraspirifer Bownockeri (Brachiopoda: Devonian)1
114 A. E. ANNALA AND L. A. KAPUSTKA Vol. 83 Copyright © 1983 Ohio Acad. Sci. 003O-O95O/83/0003-O114 $2.00/0 VERMIFORICHNUS (POLYCHAETA) BORINGS IN PARASPIRIFER BOWNOCKERI (BRACHIOPODA: DEVONIAN)1 R. D. HOARE and R. L. WALDEN, Department of Geology, Bowling Green State University, Bowling Green, OH 43403 ABSTRACT. Shells of Paraspirifer bownockeri (Stewart) from the Silica Formation, Middle Devonian of northwestern Ohio, commonly contain numerous borings of a polychaete worm forming the endolithic trace fossil Vermiforichnus clarki Cameron (1969a) which can be exposed by acidizing the specimens. The borings are most abundant on the brachial valve, and their surface openings tend to be concentrated along major growth lines thence extending dominantly in the general direction of the beaks of the valves. In- festations of the polychaete occurred at 2 different time intervals as indicated by the spac- ing of the borings on 2 major growth lines with renewed shell growth between them. Growth of the host was severely reduced immediately following the infestation and in some areas damage to the mantle caused deformation in the shell of the host. OHIO J. SCI. 83 (3): 114-119, 1983 INTRODUCTION (1932) by Hoare and Steller (1967) (fig. 1), Previous interpretations of the larger as boring sponges by Kesling and Chilman borings commonly seen in the brachiopod (1975) and as "Clionoides" sp. by Steller Paraspirifer bownockeri (Stewart) from the (1965), Kesling et al. (1980) and Sparks Silica Formation in northwestern Ohio et al. (1980). These interpretations were have been alluded to as sponge borings, based on the external configuration of the Clionoides thomasi Fenton and Fenton surface opening of the boring only. -
Identification Guide to the Planktonic Polychaete Larvae Around the Island of Helgoland (German Bight)
HELGOL.~NDER MEERESUNTERSUCHUNGEN Helgol/inder Meeresunters. 48, 1-58 (1994) Identification guide to the planktonic polychaete larvae around the island of Helgoland (German Bight) S. Plate* & E. Husemann* * Biologische Anstalt Helgoland (Meeresstation); D-27483 Helgoland, Federal Republic of Germany ABSTRACT: The purpose of this work is to provide the means of identifying the planktonic larvae of the polychaete species appearing in the plankton around the island of Helgoland (North Sea). During a three-year survey in this area, the larvae of 54 species out of 24 families belonging to the orders Orbiniida, Spionida, Capitelhda, Phyllodocida, Oweniida, Terebelhda, Sabelhda and the former Archiannelida have been recorded. Illustrated keys to the families, genera and species are presented. To facilitate the identification, additional descriptions and information about the seasonal appearance of the species are given. INTRODUCTION More than 13 000 species of polychaetous annelids take part in the marine benthos communities worldwide. Their distribution, species composition and population density are monitored within various benthos surveys. For the North Sea, especially the German Bight and the Wadden Sea, much information about the benthic polychaete fauna is available (Caspers, 1950; Stripp, 1969; DSrjes, 1977; Rachor & Gerlach, 1978; Gillandt, 1979; Salzwedel et al., 1985; Rachor, 1990; Bosselmann, 1991; Kr6ncke, 1991). In contrast, the holoplanktonic polychaete species and the meroplanktonic polychaete larvae, which are only part of the plankton during a more or less expanded phase of their ontogenesis, have never received much attention. Meroplanktonic polychaete larvae are seldomly recorded during studies monitoring the North Sea plankton (Smidt, 1951; Giere, 1968; Fransz, 1981; Bosselmann, 1989; Belgrano et al., 1990). -
Polychaete Worms Definitions and Keys to the Orders, Families and Genera
THE POLYCHAETE WORMS DEFINITIONS AND KEYS TO THE ORDERS, FAMILIES AND GENERA THE POLYCHAETE WORMS Definitions and Keys to the Orders, Families and Genera By Kristian Fauchald NATURAL HISTORY MUSEUM OF LOS ANGELES COUNTY In Conjunction With THE ALLAN HANCOCK FOUNDATION UNIVERSITY OF SOUTHERN CALIFORNIA Science Series 28 February 3, 1977 TABLE OF CONTENTS PREFACE vii ACKNOWLEDGMENTS ix INTRODUCTION 1 CHARACTERS USED TO DEFINE HIGHER TAXA 2 CLASSIFICATION OF POLYCHAETES 7 ORDERS OF POLYCHAETES 9 KEY TO FAMILIES 9 ORDER ORBINIIDA 14 ORDER CTENODRILIDA 19 ORDER PSAMMODRILIDA 20 ORDER COSSURIDA 21 ORDER SPIONIDA 21 ORDER CAPITELLIDA 31 ORDER OPHELIIDA 41 ORDER PHYLLODOCIDA 45 ORDER AMPHINOMIDA 100 ORDER SPINTHERIDA 103 ORDER EUNICIDA 104 ORDER STERNASPIDA 114 ORDER OWENIIDA 114 ORDER FLABELLIGERIDA 115 ORDER FAUVELIOPSIDA 117 ORDER TEREBELLIDA 118 ORDER SABELLIDA 135 FIVE "ARCHIANNELIDAN" FAMILIES 152 GLOSSARY 156 LITERATURE CITED 161 INDEX 180 Preface THE STUDY of polychaetes used to be a leisurely I apologize to my fellow polychaete workers for occupation, practised calmly and slowly, and introducing a complex superstructure in a group which the presence of these worms hardly ever pene- so far has been remarkably innocent of such frills. A trated the consciousness of any but the small group great number of very sound partial schemes have been of invertebrate zoologists and phylogenetlcists inter- suggested from time to time. These have been only ested in annulated creatures. This is hardly the case partially considered. The discussion is complex enough any longer. without the inclusion of speculations as to how each Studies of marine benthos have demonstrated that author would have completed his or her scheme, pro- these animals may be wholly dominant both in num- vided that he or she had had the evidence and inclina- bers of species and in numbers of specimens.