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Annelida, Hesionidae), Described As New Based on Morphometry
Contributions to Zoology, 86 (2) 181-211 (2017) Another brick in the wall: population dynamics of a symbiotic species of Oxydromus (Annelida, Hesionidae), described as new based on morphometry Daniel Martin1,*, Miguel A. Meca1, João Gil1, Pilar Drake2 & Arne Nygren3 1 Centre d’Estudis Avançats de Blanes (CEAB-CSIC) – Carrer d’Accés a la Cala Sant Francesc 14. 17300 Blanes, Girona, Catalunya, Spain 2 Instituto de Ciencias Marinas de Andalucía (ICMAN-CSIC), Avenida República Saharaui 2, Puerto Real 11519, Cádiz, Spain 3 Sjöfartsmuseet Akvariet, Karl Johansgatan 1-3, 41459, Göteborg, Sweden 1 E-mail: [email protected] Key words: Bivalvia, Cádiz Bay, Hesionidae, Iberian Peninsula, NE Atlantic Oxydromus, symbiosis, Tellinidae urn:lsid:zoobank.org:pub: D97B28C0-4BE9-4C1E-93F8-BD78F994A8D1 Abstract Results ............................................................................................. 186 Oxydromus humesi is an annelid polychaete living as a strict bi- Morphometry ........................................................................... 186 valve endosymbiont (likely parasitic) of Tellina nymphalis in Population size-structure ..................................................... 190 Congolese mangrove swamps and of Scrobicularia plana and Infestation characteristics .................................................... 190 Macomopsis pellucida in Iberian saltmarshes. The Congolese Discussion ....................................................................................... 193 and Iberian polychaete populations were previously -
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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. -
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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. -
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. -
Halosydna Brevisetosa Class: Polychaeta, Errantia
Phylum: Annelida Halosydna brevisetosa Class: Polychaeta, Errantia Order: Phyllodocida, Aphroditiformia Family: Polynoidae, Lepitonotinae Taxonomy: Eastern Pacific polynoids are Trunk: often reported with wide distributions result- Posterior: Posterior three segments ing in numerous synonymies. Although oth- with dorsal cirri. Pygidium bears one pair of er synonyms are reported, the most com- anal cirri and anus is dorsal and between seg- mon and recent for H. brevisetosa is H. ments 35–36 (Salazar-Silva 2013). johnsoni. These two species have Parapodia: Biramous. Notopodia smaller overlapping ranges centrally, but the range than neuropodia (Fig. 3). Neuropodia with of H. brevisetosa extends more northerly rounded lobe near tip of acicula. Dorsal cirri into colder waters while H. johnsoni is more expanded distally with filiform tip and ventral common in warmer, southern regions. The cirri are short, with fine tip (Salazar-Silva variation in setal morphology between them 2013). was once believed to be temperature- Setae (chaetae): All setae simple. Notosetae induced and they were synonymized short and serrate. Neorsetae falcate, with (Gaffney 1973). However, after analyzing rows of spines toward the tips, which are en- type material from both species, Salazar- tire. Neurosetae more abundant than notose- Silva (2013) determined that the two are tae (Fig. 3) (Salazar-Silva 2013). different species based on the morphology Eyes/Eyespots: Two pairs of eyes present at of neurosetae and re-described them. posterior prostomium (Fig. 2). Anterior Appendages: Three anterior anten- Description nae (Fig. 2) and two palps (Halosynda, Sala- Size: Average size range is 40 to 100 mm in zar-Silva 2013). length (Hartman 1968). -
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.). -
For Cage Aquaculture
Strengthening and supporting further development of aquaculture in the Kingdom of Saudi Arabia PROJECT UTF/SAU/048/SAU Guidelines on Environmental Monitoring for Cage Aquaculture within the Kingdom of Saudi Arabia Cover photograph: Aerial view of the floating cage farm of Tharawat Sea Company, Medina Province, Kingdom of Saudi Arabia. (courtesy Nikos Keferakis) Guidelines on environmental monitoring for cage aquaculture within the Kingdom of Saudi Arabia RICHARD ANTHONY CORNER FAO Consultant The Technical Cooperation and Partnership between the Ministry of Environment, Water and Agriculture in the Kingdom of Saudi Arabia and the Food and Agriculture Organization of the United Nations The designations employed and the presentation of material in this information product do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations (FAO), or of the Ministry of Environment, Water and Agriculture in the Kingdom of Saudi Arabia concerning the legal or development status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. The mention of specic companies or products of manufacturers, whether or not these have been patented, does not imply that these have been endorsed or recommended by FAO, or the Ministry in preference to others of a similar nature that are not mentioned. The views expressed in this information product are those of the author(s) and do not necessarily reect the views or policies of FAO, or the Ministry. ISBN 978-92-5-109651-2 (FAO) © FAO, 2017 FAO encourages the use, reproduction and dissemination of material in this information product. -
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. -
An Annotated Checklist of the Marine Macroinvertebrates of Alaska David T
NOAA Professional Paper NMFS 19 An annotated checklist of the marine macroinvertebrates of Alaska David T. Drumm • Katherine P. Maslenikov Robert Van Syoc • James W. Orr • Robert R. Lauth Duane E. Stevenson • Theodore W. Pietsch November 2016 U.S. Department of Commerce NOAA Professional Penny Pritzker Secretary of Commerce National Oceanic Papers NMFS and Atmospheric Administration Kathryn D. Sullivan Scientific Editor* Administrator Richard Langton National Marine National Marine Fisheries Service Fisheries Service Northeast Fisheries Science Center Maine Field Station Eileen Sobeck 17 Godfrey Drive, Suite 1 Assistant Administrator Orono, Maine 04473 for Fisheries Associate Editor Kathryn Dennis National Marine Fisheries Service Office of Science and Technology Economics and Social Analysis Division 1845 Wasp Blvd., Bldg. 178 Honolulu, Hawaii 96818 Managing Editor Shelley Arenas National Marine Fisheries Service Scientific Publications Office 7600 Sand Point Way NE Seattle, Washington 98115 Editorial Committee Ann C. Matarese National Marine Fisheries Service James W. Orr National Marine Fisheries Service The NOAA Professional Paper NMFS (ISSN 1931-4590) series is pub- lished by the Scientific Publications Of- *Bruce Mundy (PIFSC) was Scientific Editor during the fice, National Marine Fisheries Service, scientific editing and preparation of this report. NOAA, 7600 Sand Point Way NE, Seattle, WA 98115. The Secretary of Commerce has The NOAA Professional Paper NMFS series carries peer-reviewed, lengthy original determined that the publication of research reports, taxonomic keys, species synopses, flora and fauna studies, and data- this series is necessary in the transac- intensive reports on investigations in fishery science, engineering, and economics. tion of the public business required by law of this Department. -
Life Cycle of the Symbiotic Scaleworm Arctonoe Vittata (Polychaeta: Polynoidae)
Ophelia Suppl. 5: 305-312 (February 1991) Life Cycle of the Symbiotic Scaleworm Arctonoe vittata (Polychaeta: Polynoidae) T A . Britayev A.N. Severtzov Institute of Animal Morphology and Ecology Lenin Avenue 33, Moscow W-71, U.S.S .R . ABSTRACT The reproductive biology, some stages of de velopment, size structure, distribution by hosts, behaviour and tr aumatism were studied in a population of Arctonoeoittata at Vostok Bay (Sea ofJapan). The species is associat ed with the starfish Asterias amurensis and the limpet A cmaea pallida. It is a polytelic species with an annual reproductive cycle. Spawning occu rs during June and July. Larval development is planktotrophic and lasts about a month. Distribution of young specimens is random as a result of settlement. Analysis of different size groups of sym bionts on starfish reveals a uniformity in their distribution, wh ich is increased due to the size of the pol ynoids. Intraspecific aggressive behaviour is characteri stic for thi s spe cies. Aggressive interactions among the worms stim ula te one or mor e of them to leave a host and move onto another host - mollu sc or starfish - result ing in a uniform distribution oflarge symbionts on the hosts . For at lea st part of the symbiont population, the starfish Astenas amurensis serv es as the intermediate host and the limpet Acmaea pallida as the definitive host. Keyword s: Polychaeta, Polynoid ae, Arctonoe, sym bionts, intraspecific aggression, distribution, reproduction. INTRODUCTION The genus ArctonoeChamberlin includes three species: the typ e speciesA. vittata (Grube), A . pulchra (johnson) and A . jragilis (Baird) (Pettibone 1953: 56-66 , pis.