Halosydna Brevisetosa Class: Polychaeta, Errantia
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Phylogeny and Biogeography of Branchipolynoe
Phylogeny and Biogeography of Branchipolynoe (Polynoidae, Phyllodocida, Aciculata, Annelida), with Descriptions of Five New Species from Methane Seeps and Hydrothermal Vents Johanna Lindgren, Avery Hatch, Stéphane Hourdez, Charlotte Seid, Greg Rouse To cite this version: Johanna Lindgren, Avery Hatch, Stéphane Hourdez, Charlotte Seid, Greg Rouse. Phylogeny and Biogeography of Branchipolynoe (Polynoidae, Phyllodocida, Aciculata, Annelida), with Descriptions of Five New Species from Methane Seeps and Hydrothermal Vents. Diversity, MDPI, 2019, 11 (9), pp.153. 10.3390/d11090153. hal-02313505 HAL Id: hal-02313505 https://hal.sorbonne-universite.fr/hal-02313505 Submitted on 11 Oct 2019 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. diversity Article Phylogeny and Biogeography of Branchipolynoe (Polynoidae, Phyllodocida, Aciculata, Annelida), with Descriptions of Five New Species from Methane Seeps and Hydrothermal Vents Johanna Lindgren 1, Avery S. Hatch 1, Stephané Hourdez 2, Charlotte A. Seid 1 and Greg W. Rouse 1,* 1 Scripps Institution of Oceanography, -
Reproductive Attributes of Polynoid Polychaetes from Hydrothermal Vents on the East Pacific Rise
W&M ScholarWorks Dissertations, Theses, and Masters Projects Theses, Dissertations, & Master Projects 2005 Reproductive Attributes of Polynoid Polychaetes from Hydrothermal Vents on the East Pacific Rise Jessica Lynn Wallace College of William & Mary - Arts & Sciences Follow this and additional works at: https://scholarworks.wm.edu/etd Part of the Marine Biology Commons, and the Oceanography Commons Recommended Citation Wallace, Jessica Lynn, "Reproductive Attributes of Polynoid Polychaetes from Hydrothermal Vents on the East Pacific Rise" (2005). Dissertations, Theses, and Masters Projects. Paper 1539626835. https://dx.doi.org/doi:10.21220/s2-zy51-8j97 This Thesis is brought to you for free and open access by the Theses, Dissertations, & Master Projects at W&M ScholarWorks. It has been accepted for inclusion in Dissertations, Theses, and Masters Projects by an authorized administrator of W&M ScholarWorks. For more information, please contact [email protected]. REPRODUCTIVE ATTRIBUTES OF POLYNOID POLYCHAETES FROM HYDROTHERMAL VENTS ON THE EAST PACIFIC RISE A Thesis Presented to The Faculty of the Department of Biology The College of William and Mary in Virginia In Partial Fulfillment Of the Requirements for the Degree of Master of Science by Jessica Lynn Wallace 2005 APPROVAL SHEET This thesis is submitted in partial fulfillment of the requirements for the degree of Master of Science Jessica L. Wallace Approved by the Committee, August 2005 Dr. Cindy Lee Van Dover, Chair Dr. Paul D. Heideman Dr. Joseph L. Scott To Dad and Ken for inspiring my love of oceanography To Mom and Stephen for their unending love and support TABLE OF CONTENTS Page Acknowledgements v List of Figures vi Abstract vii Introduction 2 Chapter I. -
(Polychaeta) from the CANARY ISLANDS
BULLETIN OF MARINE SCIENCE, 48(2): l8D-188, 1991 POL YNOIDAE (pOLYCHAETA) FROM THE CANARY ISLANDS M. C. Brito, J. Nunez and J. J. Bacallado ABSTRACT This paper is a contribution to the study of the family Polynoidae (Polychaeta) from the Canary Islands. The material examined has been collected by the authors from 1975 to 1989. A total of 18 species was found belonging to 8 genera: Gesiel/a (I), Po/ynoe (1), Adyte (I), Subadyte (I), Harrnothoe (11), A/entia (1), Lepidasthenia (1) and Lepidonotus (I). Ten species are new to this fauna and one, Harrnothoe cascabullico/a, is new to science. Furthermore, the genera Po/ynoe, Adyte and Lepidasthenia are recorded for the first time in the Canary Islands. The Polychaeta of the Canary Islands are enumerated in the provisional cata- logue of Nunez et al. (1984), in which are recorded 148 species, 12 of which belong to the family Polynoidae. Samples from the Canary coastline were examined and members ofPolynoidae studied. A total of 173 specimens was studied, belonging to 7 subfamilies, 8 genera, and 18 species, of which 9 species are recorded for the first time in the Canarian fauna. Worthy of note is the large number of species belonging to the genus Harmothoe (11), one of which, H. cascabullicola is new. METHODS The material examined was collected from 1975 to 1989, from 61 stations, at 45 localities on the Canary coasts (Fig. I). The list of stations, with their localities, types of substrate and collecting data are listed in Table I. The methods used in collecting depended on the type of substrate. -
Comparative Composition, Diversity and Trophic Ecology of Sediment Macrofauna at Vents, Seeps and Organic Falls
Review Comparative Composition, Diversity and Trophic Ecology of Sediment Macrofauna at Vents, Seeps and Organic Falls Angelo F. Bernardino1*, Lisa A. Levin2, Andrew R. Thurber3, Craig R. Smith4 1 Departamento de Oceanografia e Ecologia, Universidade Federal do Espı´rito Santo, Goiabeiras, Vito´ ria, Esp´ı rito Santo, Brazil, 2 Center for Marine Biodiversity and Conservation; Integrative Oceanography Division, Scripps Institution of Oceanography, La Jolla, California, United States of America,3 College of Earth, Ocean, and Atmospheric Sciences, Oregon State University, Corvallis, Oregon, United States of America,4 Department of Oceanography, School of Ocean and Earth Science and Technology, University of Hawaii, Honolulu, Hawaii, United States of America communities. Sulfide is toxic to most metazoan taxa [1,2], Abstract: Sediments associated with hydrothermal vent- although some sediment-dwelling taxa have adapted to conditions ing, methane seepage and large organic falls such as of low oxygen and appear capable of tolerating the presence of whale, wood and plant detritus create deep-sea networks sulfide. Due to high local production, metazoans in reducing of soft-sediment habitats fueled, at least in part, by the sediments in the deep sea are often released from the extreme food oxidation of reduced chemicals. Biological studies at limitation prevalent in the background community (e.g. [3]). deep-sea vents, seeps and organic falls have looked at Instead, chemical toxicity may drive infaunal community macrofaunal taxa, but there has yet to be a systematic comparison of the community-level attributes of sedi- structure. In this meta-analysis we ask which taxa are common ment macrobenthos in various reducing ecosystems. -
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. -
Reproductive Biology of the Deep
The University of Maine DigitalCommons@UMaine Marine Sciences Faculty Scholarship School of Marine Sciences 12-1-2005 Reproductive Biology of the Deep-Sea Polychaete Gorgoniapolynoe Caeciliae (Polynoidae), a Commensal Species Associated with Octocorals Kevin Eckelbarger University of Maine - Main, [email protected] Les Watling University of Maine - Main, [email protected] H. Fournier Follow this and additional works at: https://digitalcommons.library.umaine.edu/sms_facpub Repository Citation Eckelbarger, Kevin; Watling, Les; and Fournier, H., "Reproductive Biology of the Deep-Sea Polychaete Gorgoniapolynoe Caeciliae (Polynoidae), a Commensal Species Associated with Octocorals" (2005). Marine Sciences Faculty Scholarship. 106. https://digitalcommons.library.umaine.edu/sms_facpub/106 This Article is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Marine Sciences Faculty Scholarship by an authorized administrator of DigitalCommons@UMaine. For more information, please contact [email protected]. J. Mar. Biol. Ass. U.K. (2005), 85, 1425^1433 Printed in the United Kingdom Reproductive biology of the deep-sea polychaete Gorgoniapolynoe caeciliae (Polynoidae), a commensal species associated with octocorals P O K.J. Eckelbarger* , L. Watling* and Heidi Fournier O *Darling Maine Center, The University of Maine, 193 Clark’s Cove Road, Walpole, Maine 04573, USA. Department of Biology, Roger Williams College, One Old Ferry Road, Bristol, RI 02809, USA. P Corresponding author, e-mail: [email protected] Some aspects of the reproductive biology of the polychaete Gorgoniapolynoe caeciliae have been described for the ¢rst time. Gorgoniapolynoe caeciliae is a deep-sea commensal species associated with Candidella imbricata, an octocoral that populates the New England Seamount chain. -
Harmothoe Imbricata (Linnaeus, 1767)
Harmothoe imbricata (Linnaeus, 1767) Nomenclature Phylum Annelida Class Polychaeta Order Phyllodocida Family Polynoidae Aphrodita imbricata Linnaeus, 1767 Harmothoe imbricata incerta (Bobretzky, 1881) Accepted, alternate representation: Polynoe (Harmothoe) imbricata (Linnaeus, 1767) SCAMIT Ed. 11 lists H. imbricata as a species complex Synonyms (see comments section below). Distribution Type Described based on material from Iceland, although possibly just a drawing and not an Locality actual specimen (Ruff 1995). Type material considered to be lost (Barnich and Fiege 2009). Geographic Widespread throughout northern hemisphere; to Mediterranean and New Jersey in the Distribution Atlantic, and from the Yellow Sea around the Pacific Rim to southern California (Ruff 1995). Abundant in the intertidal and shallow subtidal; also found in abyssal depths (Ruff 1995). Habitat Found free-living or commensal with terebellids (Hartman 1968). Description (from Ruff 1995 unless otherwise noted) Size/Color: Length to 65mm for 39 segments. Dorsum generally a mottled brown, although color pattern is variable (see comments section). Prostomium: Prominent, acute cephalic peaks present. 2 pairs of large eyes; anterior pair beneath cephalic peaks (but visible through prostomium). Median antenna with large pigmented ceratophore; long style with subterminal swelling, scattered papillae, and filiform tip. Lateral ceratophores short, inserted ventrally. Palps to 5x length of prostomium, tapered, papillate. Elytra: 15 pairs (Barnich and Fiege 2009). Thick, suboval, completely covering dorsum. Surface with blunt microtubercles, scattered surface papillae. Lateral and posterior borders with fringe of marginal papillae (may be absent). Larger specimens with globular macrotubercles near posterior margin. Parapodia: Biramous. Notopodia rounded, tapering to pointed acicular lobe; neuropodia longer, extending to thick prechaetal lobe with emergent acicula. -
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 ......................................................................... -
Appendix 1. Bodega Marine Lab Student Reports on Polychaete Biology
Appendix 1. Bodega Marine Lab student reports on polychaete biology. Species names in reports were assigned to currently accepted names. Thus, Ackerman (1976) reported Eupolymnia crescentis, which was recorded as Eupolymnia heterobranchia in spreadsheets of current species (spreadsheets 2-5). Ackerman, Peter. 1976. The influence of substrate upon the importance of tentacular regeneration in the terebellid polychaete EUPOLYMNIA CRESCENTIS with reference to another terebellid polychaete NEOAMPHITRITE ROBUSTA in regard to its respiratory response. Student Report, Bodega Marine Lab, Library. IDS 100 ∗ Eupolymnia heterobranchia (Johnson, 1901) reported as Eupolymnia crescentis Chamberlin, 1919 changed per Lights 2007. Alex, Dan. 1972. A settling survey of Mason's Marina. Student Report, Bodega Marine Lab, Library. Zoology 157 Alexander, David. 1976. Effects of temperature and other factors on the distribution of LUMBRINERIS ZONATA in the substratum (Annelida: polychaeta). Student Report, Bodega Marine Lab, Library. IDS 100 Amrein, Yost. 1949. The holdfast fauna of MACROSYSTIS INTEGRIFOLIA. Student Report, Bodega Marine Lab, Library. Zoology 112 ∗ Platynereis bicanaliculata (Baird, 1863) reported as Platynereis agassizi Okuda & Yamada, 1954. Changed per Lights 1954 (2nd edition). ∗ Naineris dendritica (Kinberg, 1867) reported as Nanereis laevigata (Grube, 1855) (should be: Naineris laevigata). N. laevigata not in Hartman 1969 or Lights 2007. N. dendritica taken as synonymous with N. laevigata. ∗ Hydroides uncinatus Fauvel, 1927 correct per I.T.I.S. although Hartman 1969 reports Hydroides changing to Eupomatus. Lights 2007 has changed Eupomatus to Hydroides. ∗ Dorvillea moniloceras (Moore, 1909) reported as Stauronereis moniloceras (Moore, 1909). (Stauronereis to Dorvillea per Hartman 1968). ∗ Amrein reported Stylarioides flabellata, which was not recognized by Hartman 1969, Lights 2007 or the Integrated Taxonomic Information System (I.T.I.S.). -
An Updated Checklist of the Scaleworm Harmothoe (Annelida, Polynoidae) from South America, with Two New Records from Brazil
An updated checklist of the scaleworm Harmothoe (Annelida, Polynoidae) from South America, with two new records from Brazil JOSÉ ERIBERTO DE ASSIS1, 3,*, THAÍS KANANDA DA SILVA SOUZA3, JOSÉ ROBERTO BOTELHO DE SOUZA2 & MARTIN LINDSEY CHRISTOFFERSEN3 1 Departamento de Educação Básica, Prefeitura Municipal de Bayeux, Rua Santa Tereza, CEP 58306-070, Bayeux, Paraíba. 2 Departamento de Zoologia, Centro Biociências – UFPE. Av. Prof. Morais Rego, 1235, Recife, Pernambuco, Brasil. CEP: 50670–901. 3 Laboratório e Coleção de Invertebrados Paulo Young, Departamento de Sistemática e Ecologia, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba, 58059–900, João Pessoa, Paraíba, Brasil. * Corresponding author: [email protected] ----------------------------------------------------------------------------------------------------------------------- ORCIDs JEDA: https://orcid.org/0000-0002-1522-2904 TKDSS: https://orcid.org/0000-0002-4518-0864 JRBDS: https://orcid.org/0000-0002-0144-3992 MLC: https://orcid.org/0000-0001-8108-1938 ----------------------------------------------------------------------------------------------------------------------- Abstract. The family Polynoidae includes a group of scale worms which is abundant in several marine environments, and many members are associated with other invertebrates. The genus Harmothoe is one of the largest in number of species within the polynoids, with more than 150 described species. We summarize in a checklist information relative to 23 nominal species of Harmothoe from South America, with valid names, synonyms and original citations, discuss possible taxonomic problems, and provide illustrations of specimens from the northeastern coast of Brazil. Redescriptions of two species based on new specimens collected along the littoral of the State of Pernambuco, northeastern Brazil, are included. Harmotthoe fuscapinae and Harmothoe lanceocirrata are reported for the first time for Brazilian waters. Key words: Scale worms, polynoids; South Atlantic, new records. -
(Polychaeta, Polynoidae), in the White Sea
Invertebrate Zoology, 1(1): 6573 © INVERTEBRATE ZOOLOGY, 2004 Population ecology of two simpatric polychaetes, Lepidonotus squamatus and Harmothoe imbricata (Polychaeta, Polynoidae), in the White Sea Maria Plyuscheva1, Daniel Martin2, Temir Britayev1 1A. N. Severtzov Institute of Ecology and Evolution, Russian Academy of Sciences, Leninsky pr. 33, Moscow 117071, Russia. e-mail: [email protected] 2Centre dEstudis Avançats de Blanes (CSIC), carrer daccés a la Cala Sant Francesc 14, 17300 Blanes (Girona), Catalunya (Spain). e-mail: [email protected] ABSTRACT: Under the critical environmental conditions of the White Sea, Lepidonotus squamatus and Harmothoe imbricata coexist in the same habitat, often showing recurrent alternations in dominance. L. squamatus is a long-living, slow growing broadcast spawner, while H. imbricata is a short-living and quick growing species, with complex reproductive behaviour. These different life strategies may allow them to respond in a different way to the environmental limitations of the study site, this likely being the most appropriate explanation to the observed alternation in dominance. KEYWORDS: Population dynamics; growth; scale-worms; the White Sea. Ýêîëîãèÿ ïîïóëÿöèé äâóõ ñèìïàòðè÷åñêèõ âèäîâ ïîëèõåò Lepidonotus squamatus è Harmothoe imbricata (Polychaeta, Polynoidae) â Áåëîì ìîðå Ì. Â. Ïëþùåâà1, Ä. Ìàðòèí2, Ò. À. Áðèòàåâ1 1Èíñòèòóò ïðîáëåì ýêîëîãèè è ýâîëþöèè èì. À.Í. Ñåâåðöîâà, Ðîññèéñêàÿ Àêàäåìèÿ Íàóê, Ëåíèíñêèé ïð. 33, Ìîñêâà, 117071, Ðîññèÿ. e-mail: [email protected] 2Centre dEstudis Avançats de Blanes (CSIC), carrer daccés a la Cala Sant Francesc 14, 17300 Blanes (Girona), Catalunya (Spain). e-mail: [email protected] ÐÅÇÞÌÅ:  ýêñòðåìàëüíûõ óñëîâèÿõ Áåëîãî ìîðÿ,Lepidonotus squamatus è Harmothoe imbricata çàíèìàþò ñõîäíûå ýêîëîãè÷åñêèå íèøè, äåìîíñòðèðóÿ ïåðèîäè÷åñêîå ÷åðåäîâàíèå â äîìèíèðîâàíèè. -
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.