Puget Sound Polychaetes: Family Polynoidae
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Bristol Bay, Alaska
EPA 910-R-14-001C | January 2014 An Assessment of Potential Mining Impacts on Salmon Ecosystems of Bristol Bay, Alaska Volume 3 – Appendices E-J Region 10, Seattle, WA www.epa.gov/bristolbay EPA 910-R-14-001C January 2014 AN ASSESSMENT OF POTENTIAL MINING IMPACTS ON SALMON ECOSYSTEMS OF BRISTOL BAY, ALASKA VOLUME 3—APPENDICES E-J U.S. Environmental Protection Agency Region 10 Seattle, WA CONTENTS VOLUME 1 An Assessment of Potential Mining Impacts on Salmon Ecosystems of Bristol Bay, Alaska VOLUME 2 APPENDIX A: Fishery Resources of the Bristol Bay Region APPENDIX B: Non-Salmon Freshwater Fishes of the Nushagak and Kvichak River Drainages APPENDIX C: Wildlife Resources of the Nushagak and Kvichak River Watersheds, Alaska APPENDIX D: Traditional Ecological Knowledge and Characterization of the Indigenous Cultures of the Nushagak and Kvichak Watersheds, Alaska VOLUME 3 APPENDIX E: Bristol Bay Wild Salmon Ecosystem: Baseline Levels of Economic Activity and Values APPENDIX F: Biological Characterization: Bristol Bay Marine Estuarine Processes, Fish, and Marine Mammal Assemblages APPENDIX G: Foreseeable Environmental Impact of Potential Road and Pipeline Development on Water Quality and Freshwater Fishery Resources of Bristol Bay, Alaska APPENDIX H: Geologic and Environmental Characteristics of Porphyry Copper Deposits with Emphasis on Potential Future Development in the Bristol Bay Watershed, Alaska APPENDIX I: Conventional Water Quality Mitigation Practices for Mine Design, Construction, Operation, and Closure APPENDIX J: Compensatory Mitigation and Large-Scale Hardrock Mining in the Bristol Bay Watershed AN ASSESSMENT OF POTENTIAL MINING IMPACTS ON SALMON ECOSYSTEMS OF BRISTOL BAY, ALASKA VOLUME 3—APPENDICES E-J Appendix E: Bristol Bay Wild Salmon Ecosystem: Baseline Levels of Economic Activity and Values Bristol Bay Wild Salmon Ecosystem Baseline Levels of Economic Activity and Values John Duffield Chris Neher David Patterson Bioeconomics, Inc. -
Annelida, Phyllodocida)
A peer-reviewed open-access journal ZooKeys 488: 1–29Guide (2015) and keys for the identification of Syllidae( Annelida, Phyllodocida)... 1 doi: 10.3897/zookeys.488.9061 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Guide and keys for the identification of Syllidae (Annelida, Phyllodocida) from the British Isles (reported and expected species) Guillermo San Martín1, Tim M. Worsfold2 1 Departamento de Biología (Zoología), Laboratorio de Biología Marina e Invertebrados, Facultad de Ciencias, Universidad Autónoma de Madrid, Canto Blanco, 28049 Madrid, Spain 2 APEM Limited, Diamond Centre, Unit 7, Works Road, Letchworth Garden City, Hertfordshire SG6 1LW, UK Corresponding author: Guillermo San Martín ([email protected]) Academic editor: Chris Glasby | Received 3 December 2014 | Accepted 1 February 2015 | Published 19 March 2015 http://zoobank.org/E9FCFEEA-7C9C-44BF-AB4A-CEBECCBC2C17 Citation: San Martín G, Worsfold TM (2015) Guide and keys for the identification of Syllidae (Annelida, Phyllodocida) from the British Isles (reported and expected species). ZooKeys 488: 1–29. doi: 10.3897/zookeys.488.9061 Abstract In November 2012, a workshop was carried out on the taxonomy and systematics of the family Syllidae (Annelida: Phyllodocida) at the Dove Marine Laboratory, Cullercoats, Tynemouth, UK for the National Marine Biological Analytical Quality Control (NMBAQC) Scheme. Illustrated keys for subfamilies, genera and species found in British and Irish waters were provided for participants from the major national agencies and consultancies involved in benthic sample processing. After the workshop, we prepared updates to these keys, to include some additional species provided by participants, and some species reported from nearby areas. -
Morphological Investigation and Analysis of Ribosomal DNA Phylogeny of Two Scale-Worms (Polychaeta, Polynoidae) from the Gulf of Thailand
Songklanakarin J. Sci. Technol. 40 (5), 1158-1166, Sep. - Oct. 2018 Original Article Morphological investigation and analysis of ribosomal DNA phylogeny of two scale-worms (Polychaeta, Polynoidae) from the Gulf of Thailand Arin Ngamniyom1*, Rakchanok Koto2, Weerawich Wongroj3, Thayat Sriyapai1, Pichapack Sriyapai4, and Busaba Panyarachun5 1 Faculty of Environmental Culture and Eco-tourism, Srinakharinwirot University, Watthana, Bangkok, 10110 Thailand 2 Department of Biology, Faculty of Sciences, Srinakharinwirot University, Watthana, Bangkok, 10110 Thailand 3 Prasarnmit Elementary Demonstration School, Srinakharinwirot University, Watthana, Bangkok, 10110 Thailand 4 Department of Microbiology, Faculty of Sciences, Srinakharinwirot University, Watthana, Bangkok, 10110 Thailand 5 Department of Anatomy, Faculty of Medicine, Srinakharinwirot University, Watthana, Bangkok, 10110 Thailand Received: 14 December 2016; Revised: 7 June 2017; Accepted: 5 July 2017 Abstract Scale-worms are polychaetes of the family Polynoidae that are commonly distribute in marine environments. This study aims identify and introduce two scale-worms as Capitulatinoe cf. cupisetis and Eunoe cf. oerstedi from the western coast of the Gulf of Thailand. Using scanning electron microscopy of adult worms, the antennae, palps, prostomium, cirri, setigers, parapodia, saetae and elytra are described. In addition, the phylogenetic relationships of our specimens with other polychaete species were analyzed based on partial sequences of 28S, 18S and 16S ribosomal DNA (rDNA) genes. The rDNA sequences identified C. cf. cupisetis and E. cf. oerstedi were respectively recovered within Arctonoinae and Polynoinae in a monophyletic Polynoidae. The congruence or incongruence of the morphological and molecular data is discussed in the text. These findings increase the knowledge of polynoid polychaete worms in Thailand, although two scale-worms remain to be identified of the precise species. -
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, -
Supplementary Tales
Metabarcoding reveals different zooplankton communities in northern and southern areas of the North Sea Jan Niklas Macher, Berry B. van der Hoorn, Katja T. C. A. Peijnenburg, Lodewijk van Walraven, Willem Renema Supplementary tables 1-5 Table S1: Sampling stations and recorded abiotic variables recorded during the NICO 10 expedition from the Dutch Coast to the Shetland Islands Sampling site name Coordinates (°N, °E) Mean remperature (°C) Mean salinity (PSU) Depth (m) S74 59.416510, 0.499900 8.2 35.1 134 S37 58.1855556, 0.5016667 8.7 35.1 89 S93 57.36046, 0.57784 7.8 34.8 84 S22 56.5866667, 0.6905556 8.3 34.9 220 S109 56.06489, 1.59652 8.7 35 79 S130 55.62157, 2.38651 7.8 34.8 73 S156 54.88581, 3.69192 8.3 34.6 41 S176 54.41489, 4.04154 9.6 34.6 43 S203 53.76851, 4.76715 11.8 34.5 34 Table S2: Species list and read number per sampling site Class Order Family Genus Species S22 S37 S74 S93 S109 S130 S156 S176 S203 Copepoda Calanoida Acartiidae Acartia Acartia clausi 0 0 0 72 0 170 15 630 3995 Copepoda Calanoida Acartiidae Acartia Acartia tonsa 0 0 0 0 0 0 0 0 23 Hydrozoa Trachymedusae Rhopalonematidae Aglantha Aglantha digitale 0 0 0 0 1870 117 420 629 0 Actinopterygii Trachiniformes Ammodytidae Ammodytes Ammodytes marinus 0 0 0 0 0 263 0 35 0 Copepoda Harpacticoida Miraciidae Amphiascopsis Amphiascopsis cinctus 344 0 0 992 2477 2500 9574 8947 0 Ophiuroidea Amphilepidida Amphiuridae Amphiura Amphiura filiformis 0 0 0 0 219 0 0 1470 63233 Copepoda Calanoida Pontellidae Anomalocera Anomalocera patersoni 0 0 586 0 0 0 0 0 0 Bivalvia Venerida -
Onetouch 4.0 Sanned Documents
Vol. 82, pp. 1-30 29 May, 1969 PROCEEDINGS OF THE BIOLOGICAL SOCIETY OF WASHINGTON REVIEW OF SOME SPECIES REFERRED TO SCALISETOSUS MCINTOSH (POLYCHAETA, POLYNOIDAE) BY MABIAN H. PETTIBONE Smithsonian Institution, Washington, D. C. In connection with an extended review of the polynoid gen- era, based on a study of the type-species, it was foimd that Scalisetosus Mclntosh ( 1885) has been used for a heterogenous group of species. The genus has served to include species with setae as transparent as crystal and the neurosetae character- ized by the presence of a basal semilunar cusp or pocket, al- though this particular feature was not shown on the figure of the neiu-osetae of the type-species, S. ceramensis, by Mclntosh (1885, pi. lOA, fig. 14). Any species equipped with this pe- culiar type of neiu-osetae has been placed in Scalisetosus, re- gardless of other characters. Saint-Joseph (1899) proposed the new genus Adyte for three species {Polynoe pellucida Ehlers, Hermadion assimile Mclntosh, and H. echini Giard) having the peculiar type of neurosetae, separating them from S. cera- mensis, which lacks the basal semilunar cusps. Mclntosh (1900) was responsible for changing the diagnosis of Scali- setosus to include the species referred to Adyte by Saint- Joseph, Subsequently, Adyte was abandoned and was synony- mized with Scalisetosus by Fauvel (1914, p. 47). During a visit to the British Museum of Natural History in May 1967, I was able to examine the unique type of Scalise- tosus ceramensis and to verify that the neurosetae indeed do lack the basal semilunar cusps and that the species therefore lacks one of the key characters that has been attributed to the genus. -
(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. -
National Reports (Term of Reference A) Presented at the 46Th Meeting of the ICES Working Group on Introductions and Transfers Of
National Reports (Term of Reference a) Presented at the 46th meeting of the ICES Working Group on Introductions and Transfers of Marine Organisms, held in Gdynia, Poland from 4 to 6 March 2020. Arranged Alphabetically by Country Compiled by Cynthia H McKenzie, Chair, WGITMO CANADA …………………………………………………………………… …. 2 DENMARK ………………………………………………………………………. 10 FINLAND ………………………………………………………………………. 18 FRANCE ………………………………………………………………………. 21 GERMANY ………………………………………………………………………. 33 GREECE ………………………………………………………………………. 46 ICELAND ………………………………………………………………………. 54 ITALY ………………………………………………………………………. 58 LITHUANIA ………………………………………………………………………. 73 NETHERLANDS …………………………………………………………………. 75 NORWAY ………………………………………………………………………. 77 POLAND ………………………………………………………………………. 86 PORTUGAL ………………………………………………………………………. 89 SWEDEN ………………………………………………………………………. 99 UNITED KINGDOM ……………………………………………………………. 104 UNITED STATES …………………………………………………………………. 119 1 CANADA National Report for Canada 2019 Report Prepared By: Cynthia McKenzie, Fisheries and Oceans Canada, Newfoundland and Labrador Region: [email protected]; Contributions By: Nathalie Simard, Fisheries and Oceans Canada, Quebec Region: [email protected]; Kimberly Howland, Fisheries and Oceans Canada, Central and Arctic Region: [email protected]; Renée Bernier and Chantal Coomber, Fisheries and Oceans Canada, Gulf Region: renee.bernier@dfo- mpo.gc.ca, [email protected]; Angelica Silva, Fisheries and Oceans Canada, Maritimes Region: [email protected] Overview: NEW or SPREAD -
A Bioturbation Classification of European Marine Infaunal
A bioturbation classification of European marine infaunal invertebrates Ana M. Queiros 1, Silvana N. R. Birchenough2, Julie Bremner2, Jasmin A. Godbold3, Ruth E. Parker2, Alicia Romero-Ramirez4, Henning Reiss5,6, Martin Solan3, Paul J. Somerfield1, Carl Van Colen7, Gert Van Hoey8 & Stephen Widdicombe1 1Plymouth Marine Laboratory, Prospect Place, The Hoe, Plymouth, PL1 3DH, U.K. 2The Centre for Environment, Fisheries and Aquaculture Science, Pakefield Road, Lowestoft, NR33 OHT, U.K. 3Department of Ocean and Earth Science, National Oceanography Centre, University of Southampton, Waterfront Campus, European Way, Southampton SO14 3ZH, U.K. 4EPOC – UMR5805, Universite Bordeaux 1- CNRS, Station Marine d’Arcachon, 2 Rue du Professeur Jolyet, Arcachon 33120, France 5Faculty of Biosciences and Aquaculture, University of Nordland, Postboks 1490, Bodø 8049, Norway 6Department for Marine Research, Senckenberg Gesellschaft fu¨ r Naturforschung, Su¨ dstrand 40, Wilhelmshaven 26382, Germany 7Marine Biology Research Group, Ghent University, Krijgslaan 281/S8, Ghent 9000, Belgium 8Bio-Environmental Research Group, Institute for Agriculture and Fisheries Research (ILVO-Fisheries), Ankerstraat 1, Ostend 8400, Belgium Keywords Abstract Biodiversity, biogeochemical, ecosystem function, functional group, good Bioturbation, the biogenic modification of sediments through particle rework- environmental status, Marine Strategy ing and burrow ventilation, is a key mediator of many important geochemical Framework Directive, process, trait. processes in marine systems. In situ quantification of bioturbation can be achieved in a myriad of ways, requiring expert knowledge, technology, and Correspondence resources not always available, and not feasible in some settings. Where dedi- Ana M. Queiros, Plymouth Marine cated research programmes do not exist, a practical alternative is the adoption Laboratory, Prospect Place, The Hoe, Plymouth PL1 3DH, U.K. -
Polychaeta: Polynoidae) and Revision of Iphione Cimex Quatrefages, Gattyana Deludens Fauvel, and Harmothoe Iphionelloides Johnson (Harmothoinae
Review of the Iphioninae (Polychaeta: Polynoidae) and Revision of Iphione cimex Quatrefages, Gattyana deludens Fauvel, and Harmothoe iphionelloides Johnson (Harmothoinae) MARIAN H. PETTIBONE SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY • NUMBER 428 SERIES PUBLICATIONS OF THE SMITHSONIAN INSTITUTION Emphasis upon publication as a means of "diffusing knowledge" was expressed by the first Secretary of the Smithsonian. In his formal plan for the Institution, Joseph Henry outlined a program that included the following statement: "It is proposed to publish a series of reports, giving an account of the new discoveries in science, and of the changes made from year to year in all branches of knowledge." This theme of basic research has been adhered to through the years by thousands of titles issued in series publications under the Smithsonian imprint, commencing with Smithsonian Contributions to Knowledge in 1848 and continuing with the following active series: Smithsonian Contributions to Anthropology Smithsonian Contributions to Astrophysics Smithsonian Contributions to Botany Smithsonian Contributions to the Earth Sciences Smithsonian Contributions to the Marine Sciences Smithsonian Contributions to Paleobiology Smithsonian Contributions to Zoology Smithsonian Folklife Studies Smithsonian Studies in Air and Space Smithsonian Studies in History and Technology In these series, the Institution publishes small papers and full-scale monographs that report the research and collections of its various museums and bureaux or of professional colleagues in the world of science and scholarship. The publications are distributed by mailing lists to libraries, universities, and similar institutions throughout the world. Papers or monographs submitted for series publication are received by the Smithsonian Institution Press, subject to its own review for format and style, only through departments of the various Smithsonian museums or bureaux, where the manuscripts are given substantive review. -
The Biology of Seashores - Image Bank Guide All Images and Text ©2006 Biomedia ASSOCIATES
The Biology of Seashores - Image Bank Guide All Images And Text ©2006 BioMEDIA ASSOCIATES Shore Types Low tide, sandy beach, clam diggers. Knowing the Low tide, rocky shore, sandstone shelves ,The time and extent of low tides is important for people amount of beach exposed at low tide depends both on who collect intertidal organisms for food. the level the tide will reach, and on the gradient of the beach. Low tide, Salt Point, CA, mixed sandstone and hard Low tide, granite boulders, The geology of intertidal rock boulders. A rocky beach at low tide. Rocks in the areas varies widely. Here, vertical faces of exposure background are about 15 ft. (4 meters) high. are mixed with gentle slopes, providing much variation in rocky intertidal habitat. Split frame, showing low tide and high tide from same view, Salt Point, California. Identical views Low tide, muddy bay, Bodega Bay, California. of a rocky intertidal area at a moderate low tide (left) Bays protected from winds, currents, and waves tend and moderate high tide (right). Tidal variation between to be shallow and muddy as sediments from rivers these two times was about 9 feet (2.7 m). accumulate in the basin. The receding tide leaves mudflats. High tide, Salt Point, mixed sandstone and hard rock boulders. Same beach as previous two slides, Low tide, muddy bay. In some bays, low tides expose note the absence of exposed algae on the rocks. vast areas of mudflats. The sea may recede several kilometers from the shoreline of high tide Tides Low tide, sandy beach. -
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).