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Molecular Phylogeny of Echiuran Worms (Phylum: Annelida) Reveals Evolutionary Pattern of Feeding Mode and Sexual Dimorphism
Molecular Phylogeny of Echiuran Worms (Phylum: Annelida) Reveals Evolutionary Pattern of Feeding Mode and Sexual Dimorphism Ryutaro Goto1,2*, Tomoko Okamoto2, Hiroshi Ishikawa3, Yoichi Hamamura4, Makoto Kato2 1 Department of Marine Ecosystem Dynamics, Atmosphere and Ocean Research Institute, The University of Tokyo, Kashiwa, Chiba, Japan, 2 Graduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan, 3 Uwajima, Ehime, Japan, 4 Kure, Hiroshima, Japan Abstract The Echiura, or spoon worms, are a group of marine worms, most of which live in burrows in soft sediments. This annelid- like animal group was once considered as a separate phylum because of the absence of segmentation, although recent molecular analyses have placed it within the annelids. In this study, we elucidate the interfamily relationships of echiuran worms and their evolutionary pattern of feeding mode and sexual dimorphism, by performing molecular phylogenetic analyses using four genes (18S, 28S, H3, and COI) of representatives of all extant echiuran families. Our results suggest that Echiura is monophyletic and comprises two unexpected groups: [Echiuridae+Urechidae+Thalassematidae] and [Bone- lliidae+Ikedidae]. This grouping agrees with the presence/absence of marked sexual dimorphism involving dwarf males and the paired/non-paired configuration of the gonoducts (genital sacs). Furthermore, the data supports the sister group relationship of Echiuridae and Urechidae. These two families share the character of having anal chaetae rings around the posterior trunk as a synapomorphy. The analyses also suggest that deposit feeding is a basal feeding mode in echiurans and that filter feeding originated once in the common ancestor of Urechidae. Overall, our results contradict the currently accepted order-level classification, especially in that Echiuroinea is polyphyletic, and provide novel insights into the evolution of echiuran worms. -
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. -
Zootaxa, Loandalia (Polychaeta: Pilargidae)
Zootaxa 1119: 59–68 (2006) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1119 Copyright © 2006 Magnolia Press ISSN 1175-5334 (online edition) New species of Loandalia (Polychaeta: Pilargidae) from Queensland, Australia SHONA MARKS1 & SCOTT HOCKNULL2 1 S. A. Marks. CSIRO Marine Research, PO Box 120, Cleveland QLD 4163. [email protected]. 2 S. A. Hocknull. Queensland Museum, 122 Gerler Rd Hendra QLD 4711. [email protected] Abstract Two new species of Loandalia are described from Queensland, Australia. Loandalia fredrayorum sp. nov. is described from Moreton Bay, south eastern Queensland and is distinguished from all other species of Loandalia by the presence of singular palpostyles; uniramous parapodia at chaetiger 1; an emergent notopodial spine at chaetiger 9; neurochaetae numbering 20–24; ventral cirri begin on chaetiger 7 and the pygidium with two lateral papillae-like anal cirri. Loandalia gladstonensis sp. nov. is described from Gladstone Harbour, central eastern Queensland and is distinguished from all other species of Loandalia by the presence of bifid palpostyles; chaetiger 1 uniramous with remaining chaetigers biramous; an emergent notopodial spine from chaetiger 7–8; ventral cirri present from chaetiger 5 and neurochaetae numbering 5–6. Key words: Loandalia fredrayorum sp. nov., Loandalia gladstonensis sp.nov., Pilargidae, Queensland, Australia, new species, systematics. Introduction Saint-Joseph (1899) established the Pilargidae for the new species Pilargis verrucosa Saint-Joseph. Prior to this, pilargids had been placed in several different families including the Syllidae, Hesionidae and Polynoidae (Licher & Westheide 1994). Recent cladistic analyses of the Phyllodocida firmly recognise Pilargidae as a distinct clade (Glasby 1993; Pleijel & Dahlgren 1998). -
Molecular Phylogeny of the Family Capitellidae (Annelida)
Title Molecular Phylogeny of the Family Capitellidae (Annelida) Author(s) Tomioka, Shinri; Kakui, Keiichi; Kajihara, Hiroshi Zoological Science, 35(5), 436-445 Citation https://doi.org/10.2108/zs180009 Issue Date 2018-10 Doc URL http://hdl.handle.net/2115/75605 Type article File Information Zoological Science35-5_436‒445(2018).pdf Instructions for use Hokkaido University Collection of Scholarly and Academic Papers : HUSCAP ZOOLOGICAL436 SCIENCE 35: 436–445 (2018) S. Tomioka et al. © 2018 Zoological Society of Japan Molecular Phylogeny of the Family Capitellidae (Annelida) Shinri Tomioka1*, Keiichi Kakui2, and Hiroshi Kajihara2 1Rishiri Town Museum, Senhoshi, Rishiri Is., Hokkaido 097-0311, Japan 2Department of Biological Sciences, Faculty of Science, Hokkaido University, N10 W8, Sapporo, Hokkaido 060-0810, Japan Capitellids have emerged as monophyletic in most but not all recent molecular phylogenies, indi- cating that more extensive taxon sampling is necessary. In addition, monophyly of most or all capitellid genera was questionable, as some diagnostic characters vary ontogenetically within individuals. We tested the monophyly of Capitellidae and eight capitellid genera using phyloge- netic analyses of combined 18S, 28S, H3, and COI gene sequences from 36 putative capitellid spe- cies. In our trees, Capitellidae formed a monophyletic sister group to Echiura, and Capitella was also monophyletic, separated by a long branch from other capitellids. Well-supported clades each containing representatives of different genera, or containing a subset of species within a genus, indicated that Barantolla, Heteromastus, and Notomastus are likely not monophyletic. We mapped three morphological characters traditionally used to define capitellid genera (head width relative to width of first segment, number of thoracic segments, and number of segments with capillary chae- tae) onto our tree. -
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 ......................................................................... -
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. -
Of Polychaetes (Annelida: Polychaeta) from the Atlantic and Mediterranean Coasts of the Iberian Peninsula: an Annotated Checklist E
López and Richter Helgol Mar Res (2017) 71:19 DOI 10.1186/s10152-017-0499-6 Helgoland Marine Research ORIGINAL ARTICLE Open Access Non‑indigenous species (NIS) of polychaetes (Annelida: Polychaeta) from the Atlantic and Mediterranean coasts of the Iberian Peninsula: an annotated checklist E. López* and A. Richter Abstract This study provides an updated catalogue of non-indigenous species (NIS) of polychaetes reported from the conti- nental coasts of the Iberian Peninsula based on the available literature. A list of 23 introduced species were regarded as established and other 11 were reported as casual, with 11 established and nine casual NIS in the Atlantic coast of the studied area and 14 established species and seven casual ones in the Mediterranean side. The most frequent way of transport was shipping (ballast water or hull fouling), which according to literature likely accounted for the intro- ductions of 14 established species and for the presence of another casual one. To a much lesser extent aquaculture (three established and two casual species) and bait importation (one established species) were also recorded, but for a large number of species the translocation pathway was unknown. About 25% of the reported NIS originated in the Warm Western Atlantic region, followed by the Tropical Indo West-Pacifc region (18%) and the Warm Eastern Atlantic (12%). In the Mediterranean coast of the Iberian Peninsula, nearly all the reported NIS originated from warm or tropi- cal regions, but less than half of the species recorded from the Atlantic side were native of these areas. The efects of these introductions in native marine fauna are largely unknown, except for one species (Ficopomatus enigmaticus) which was reported to cause serious environmental impacts. -
Bathyal and Abyssal Polychaetes (Annelids) from the Central Coast of Oregon
AN ABSTRACT OF THE THESIS OF DANIL RAY HANCOCK for the MASTER OF SCIENCE (Name) (Degree) in OCEANOGRAPHY presented on (Major) (Date) Title: BATHYAL AND ABYSSAL POLYCIiAETES (ANNELIDS) FROM THE CENTRAL COAST OF OREGON Abstract approved Redacted for Privacy Andtew G. Ca4ey, Jr. Polychaete annelids from 48 benthic samples containing over 2000 specimens were identified.Samples were taken with either an anchor dredge or an anchor-box dredge from a 15 station transect (44° 39. l'N) that ranges from 800 to 2900 meters in depth.Sediment subsamples were collected and analyzed for organic carbon and sedi- ment particle size using standard techniques.Temperature and oxygen of the water near the bottom were taken with a modified Smith- McIntyre grab; however, these measurements were not taken simultaneously with the dredged biological samples. The results indicated that at least 115 species in 53 families of the class Polychaeta were represented in this transect line.This study found an absence of the families Serpulidae and Syllidae and a reduction of the number of speciesin the families Nereidae, Cirratulidae and Capitellidae.Only five genera had not previously been reported from the deep sea.The depth distribution of the polychaetous annelids recovered in this study, coupled with limited physical data, suggest that five faunal regions can be distinguished. Nine new forms of polychaeteous annelids are tentativelydescribed, and others are anticipated in future collections.Suggestions for future studies are also indicated. Bathyal and Abyssal Polychaetes -
Catalogue of Notomastus M. Sars, 1851 (Annelida, Capitellidae) and the Description of a New Species from the Gulf of California
Zootaxa 4577 (2): 249–273 ISSN 1175-5326 (print edition) https://www.mapress.com/j/zt/ Article ZOOTAXA Copyright © 2019 Magnolia Press ISSN 1175-5334 (online edition) https://doi.org/10.11646/zootaxa.4577.2.2 http://zoobank.org/urn:lsid:zoobank.org:pub:C61988A5-561D-4E34-9C0B-2E8BFF23BF25 Catalogue of Notomastus M. Sars, 1851 (Annelida, Capitellidae) and the description of a new species from the Gulf of California MARÍA ELENA GARCÍA-GARZA1,2, JESÚS ANGEL DE LEÓN-GONZÁLEZ1 & MARÍA ANA TOVAR-HERNÁNDEZ1 1Universidad Autónoma de Nuevo León, Facultad de Ciencias Biológicas, Laboratorio de Biosistemática, San Nicolás de los Garza, Nuevo León, México. 2Corresponding author. E-mail: [email protected]. Phone number: +52 (81) 83-294110 ext. 6463. ORCID 0000-0002-9022-2728 Abstract Capitellids are burrowing, earthworm-like polychaetes. The taxonomy within the group presents significant difficulties, due in part to their relative simplicity. In this study, a catalogue of the capitellid genus Notomastus M. Sars, 1851, is pre- sented and a new species is described from the Southern Gulf of California: Notomastus mazatlanensis sp. nov. The cat- alogue provides original names and synonymies for 43 species; type locality and location of type materials; records and remarks on systematics and distribution. Type material of 35 species were examined, 31 from which were photographed to illustrate the catalogue. Notomastus mazatlanensis sp. nov. is established based on the presence of finger-like branchiae emerging from the epithelium near to the notopodia. Branchiae are composed by 3–4 filaments, and the first chaetiger is uniramous. A taxonomic key for species distributed in the Gulf of California is presented. -
Symbiontsms Final
being cryptic. Accordingly, this fauna tends to remain virtually unknown, especially in Scale-worms (Polychaeta, Polynoidae) associated with tropical and deep waters. chaetopterid worms (Polychaeta, Chaetopteridae), with Among marine animals, the class Polychaeta includes one of the highest number description of a new genus and species of symbiotic species, with more than 370 symbionts according to Martin and Britayev (1998). Symbiotic polychaetes are associated with nearly all main taxa of marine metazoans (excluding flatworms, nemerteans and nematodes) and even with protozoans. + *± T. A. BRITAYEV and D. MARTIN However, they clearly prefer organisms providing them with good shelter, such as burrowing or tube-dwelling animals (viz. sipunculids, balanoglossids, tubicolous + A.N. Severtzov Institute of Ecology and Evolution (RAS), Leninsky pr. 33, 117071 Moscow, Russia. polychaetes). The durable and long tubes of chaetopterid worms (Polychaeta, Telephone: +0951247950. Fax: +0959545554. E-mail: [email protected] Chaetopteridae) probably offer one of the most “comfortable” habitats for symbiotic ±* Centre d’Estudis Avançats de Blanes (CSIC), carrer d’accés a la Cala Sant Francesc 14, Blanes (Girona), Catalunya (Spain). Telephone: +34972336101. Fax: +34972337806. E-mail: [email protected] polychaetes (Petersen & Britayev 1997) and shelter at least 17 species of facultative and obligate polychaete species (Martin & Britayev 1998). Three species of scale-worms inhabiting chaetopterid tubes have been found during routine studies During studies of the structure of bottom communities performed by the authors of benthic communities. Anotochaetonoe michelbhaudi gen. et sp. nov. occurred in the E Atlantic along the coasts of Congo (Atlantic Ocean), France (Mediterranean Sea) and Vietnam off Congo in association with Spiochaetopterus sp. -
Annelida: Phyllodocida: Pilargidae) from Northern Australia and New Guinea
The Beagle, Records of the Museums and Art Galleries of the Northern Territory, 2010 26: 57–67 New records and a new species of Hermundura Müller, 1858, the senior synonym of Loandalia Monro, 1936 (Annelida: Phyllodocida: Pilargidae) from northern Australia and New Guinea Christopher J. Glasby1 and Shona A. Hocknull2 1Museum and Art Gallery of the Northern Territory, GPO Box 4646, Darwin NT 0801, AUSTRALIA [email protected] 2Benthic Australia, PO Box 5354, Manly QLD 4197, AUSTRALIA [email protected] ABSTRACT The Principle of Priority (ICZN 1999) is applied in resurrecting the generic name Hermundura Müller, 1858 for pilargid polychaetes (Annelida) formerly referred to as Loandalia Monro, 1936 and Parandalia Emerson & Fauchald, 1971. All available specimens of Hermundura from northern Australia and New Guinea are described based on material held in the collections of Australia’s natural history museums. Our study recognises two species, H. gladstonensis (Marks & Hocknull, 2006) comb. nov. and a new species, H. philipi sp. nov., from near Mornington Island in the southern Gulf of Carpentaria. The former species is redescribed, and new information on intraspecific variability is provided, including the presence of hardened, cuticular structures and a muscle band (sphincter) of the anterior alimentary canal. Analysis of these structures has led to a re-evaluation of the so-called ‘jaws’ of the closely related monotypic genus Talehsapia Fauvel, 1932, and the conclusion that they are homologous with the pharyngeal sphincter of Hermundura. Talehsapia therefore is also synonymised with Hermundura. The genus Hermundura now contains 17 species including the type species, Hermundura tricuspis Müller, 1858, H. -
Annelida: Chaetopteridae)
Do syntopic host species harbour similar symbiotic communities? The case of Chaetopterus spp. (Annelida: Chaetopteridae) Temir A. Britayev1, Elena Mekhova1, Yury Deart1 and Daniel Martin2 1 Severtzov Institute of Ecology and Evolution, Russian Academy of Sciences, Moscow, Russian Federation 2 Department of Marine Ecology, Centre d'Estudis Avancats¸ de Blanes (CEAB–CSIC), Blanes, Catalunya, Spain ABSTRACT To assess whether closely related host species harbour similar symbiotic commu- nities, we studied two polychaetes, Chaetopterus sp. (n D 11) and Chaetopterus cf. appendiculatus (n D 83) living in soft sediments of Nhatrang Bay (South China Sea, Vietnam). The former harboured the porcellanid crabs Polyonyx cf. heok and Polyonyx sp., the pinnotherid crab Tetrias sp. and the tergipedid nudibranch Phestilla sp. The latter harboured the polynoid polychaete Ophthalmonoe pettiboneae, the carapid fish Onuxodon fowleri and the porcellanid crab Eulenaios cometes, all of which, except O. fowleri, seemed to be specialized symbionts. The species richness and mean intensity of the symbionts were higher in Chaetopterus sp. than in C. cf. appendiculatus (1.8 and 1.02 species and 3.0 and 1.05 individuals per host respectively). We suggest that the lower density of Chaetopterus sp. may explain the higher number of associated symbionts observed, as well as the 100% prevalence (69.5% in C. cf. appenciculatus). Most Chaetopterus sp. harboured two symbiotic species, which was extremely rare in C. cf. appendiculatus, suggesting lower interspecific interactions in the former. The crab and nudibranch symbionts of Chaetopterus sp. often shared a host and lived in pairs, thus partitioning resources. This led to the species coexisting in the tubes Submitted 10 October 2016 of Chaetopterus sp., establishing a tightly packed community, indicating high species Accepted 21 December 2016 richness and mean intensity, together with a low species dominance.