Puget Sound Intertidal Biotic Community Monitoring 2011
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Appendix to Taxonomic Revision of Leopold and Rudolf Blaschkas' Glass Models of Invertebrates 1888 Catalogue, with Correction
http://www.natsca.org Journal of Natural Science Collections Title: Appendix to Taxonomic revision of Leopold and Rudolf Blaschkas’ Glass Models of Invertebrates 1888 Catalogue, with correction of authorities Author(s): Callaghan, E., Egger, B., Doyle, H., & E. G. Reynaud Source: Callaghan, E., Egger, B., Doyle, H., & E. G. Reynaud. (2020). Appendix to Taxonomic revision of Leopold and Rudolf Blaschkas’ Glass Models of Invertebrates 1888 Catalogue, with correction of authorities. Journal of Natural Science Collections, Volume 7, . URL: http://www.natsca.org/article/2587 NatSCA supports open access publication as part of its mission is to promote and support natural science collections. NatSCA uses the Creative Commons Attribution License (CCAL) http://creativecommons.org/licenses/by/2.5/ for all works we publish. Under CCAL authors retain ownership of the copyright for their article, but authors allow anyone to download, reuse, reprint, modify, distribute, and/or copy articles in NatSCA publications, so long as the original authors and source are cited. TABLE 3 – Callaghan et al. WARD AUTHORITY TAXONOMY ORIGINAL SPECIES NAME REVISED SPECIES NAME REVISED AUTHORITY N° (Ward Catalogue 1888) Coelenterata Anthozoa Alcyonaria 1 Alcyonium digitatum Linnaeus, 1758 2 Alcyonium palmatum Pallas, 1766 3 Alcyonium stellatum Milne-Edwards [?] Sarcophyton stellatum Kükenthal, 1910 4 Anthelia glauca Savigny Lamarck, 1816 5 Corallium rubrum Lamarck Linnaeus, 1758 6 Gorgonia verrucosa Pallas, 1766 [?] Eunicella verrucosa 7 Kophobelemon (Umbellularia) stelliferum -
COMPLETE LIST of MARINE and SHORELINE SPECIES 2012-2016 BIOBLITZ VASHON ISLAND Marine Algae Sponges
COMPLETE LIST OF MARINE AND SHORELINE SPECIES 2012-2016 BIOBLITZ VASHON ISLAND List compiled by: Rayna Holtz, Jeff Adams, Maria Metler Marine algae Number Scientific name Common name Notes BB year Location 1 Laminaria saccharina sugar kelp 2013SH 2 Acrosiphonia sp. green rope 2015 M 3 Alga sp. filamentous brown algae unknown unique 2013 SH 4 Callophyllis spp. beautiful leaf seaweeds 2012 NP 5 Ceramium pacificum hairy pottery seaweed 2015 M 6 Chondracanthus exasperatus turkish towel 2012, 2013, 2014 NP, SH, CH 7 Colpomenia bullosa oyster thief 2012 NP 8 Corallinales unknown sp. crustous coralline 2012 NP 9 Costaria costata seersucker 2012, 2014, 2015 NP, CH, M 10 Cyanoebacteria sp. black slime blue-green algae 2015M 11 Desmarestia ligulata broad acid weed 2012 NP 12 Desmarestia ligulata flattened acid kelp 2015 M 13 Desmerestia aculeata (viridis) witch's hair 2012, 2015, 2016 NP, M, J 14 Endoclaydia muricata algae 2016 J 15 Enteromorpha intestinalis gutweed 2016 J 16 Fucus distichus rockweed 2014, 2016 CH, J 17 Fucus gardneri rockweed 2012, 2015 NP, M 18 Gracilaria/Gracilariopsis red spaghetti 2012, 2014, 2015 NP, CH, M 19 Hildenbrandia sp. rusty rock red algae 2013, 2015 SH, M 20 Laminaria saccharina sugar wrack kelp 2012, 2015 NP, M 21 Laminaria stechelli sugar wrack kelp 2012 NP 22 Mastocarpus papillatus Turkish washcloth 2012, 2013, 2014, 2015 NP, SH, CH, M 23 Mazzaella splendens iridescent seaweed 2012, 2014 NP, CH 24 Nereocystis luetkeana bull kelp 2012, 2014 NP, CH 25 Polysiphonous spp. filamentous red 2015 M 26 Porphyra sp. nori (laver) 2012, 2013, 2015 NP, SH, M 27 Prionitis lyallii broad iodine seaweed 2015 M 28 Saccharina latissima sugar kelp 2012, 2014 NP, CH 29 Sarcodiotheca gaudichaudii sea noodles 2012, 2014, 2015, 2016 NP, CH, M, J 30 Sargassum muticum sargassum 2012, 2014, 2015 NP, CH, M 31 Sparlingia pertusa red eyelet silk 2013SH 32 Ulva intestinalis sea lettuce 2014, 2015, 2016 CH, M, J 33 Ulva lactuca sea lettuce 2012-2016 ALL 34 Ulva linza flat tube sea lettuce 2015 M 35 Ulva sp. -
Onchidoris Bilamellata Class: Gastropoda, Opisthobranchia Order: Nudibranchia Many-Gilled Onchidoris Nudibranch Family: Onchidoridae
Phylum: Mollusca Onchidoris bilamellata Class: Gastropoda, Opisthobranchia Order: Nudibranchia Many-gilled onchidoris nudibranch Family: Onchidoridae Description Papillae: Mushroom-shaped, with protruding Size: Usual length 15 mm (McDonald 1980); spicules (Fig. 3). Numerous club-like this specimen 15.5 mm long, 11 mm wide, 6 tubercles of unequal size with a slight convex mm high. Far northern and Atlantic specimens top. 10-15 spicules covered with epithelium can reach 31 mm length (Marcus 1961). project out over the surface. Spicules are Color: Translucent brownish-white with thick with blunt tips and are centrally bent, irregular dark or rusty brown splotches, sloping obliquely toward the base of the sometimes as irregular longitudinal stripes. tubercle (Kress 1981). Spicules support the Commonly a light spot between the dark body and make it unpalatable (Potts 1981). rhinophores; gills dull white, underside a dull Eggs: Type A, defined as an egg mass in white (Marcus 1961). No yellow pigment, but ribbon form, attached along the length of one some specimens without brown color (Kozloff edge, with capsules occurring throughout 1974). Cryptic coloration (Potts 1981). (Hurst 1967). With a short, stout spiral ribbon Body Shape: Doridiform: oval; slightly attached along one edge, flaring out on the broadened towards front. With a broad flat other (O’Donoghue and O’Donoghue 1922) foot, thick fleshy mantle, and conspicuous (Fig. 5); capsules have a smooth wall and double circlet of gills dorsally (Figs. 1, 2). contain 1-3 eggs; 60,000 eggs in a ribbon 4 Dorsum covered with many large round cm long (Hadfield 1963). Eggs 100µm. Eggs papillae, becoming smaller at edges. -
Venerupis Philippinarum)
INVESTIGATING THE COLLECTIVE EFFECT OF TWO OCEAN ACIDIFICATION ADAPTATION STRATEGIES ON JUVENILE CLAMS (VENERUPIS PHILIPPINARUM) Courtney M. Greiner A Swinomish Indian Tribal Community Contribution SWIN-CR-2017-01 September 2017 La Conner, WA 98257 Investigating the collective effect of two ocean acidification adaptation strategies on juvenile clams (Venerupis philippinarum) Courtney M. Greiner A thesis submitted in partial fulfillment of the requirements for the degree of Master of Marine Affairs University of Washington 2017 Committee: Terrie Klinger Jennifer Ruesink Program Authorized to Offer Degree: School of Marine and Environmental Affairs ©Copyright 2017 Courtney M. Greiner University of Washington Abstract Investigating the collective effect of two ocean acidification adaptation strategies on juvenile clams (Venerupis philippinarum) Courtney M. Greiner Chair of Supervisory Committee: Dr. Terrie Klinger School of Marine and Environmental Affairs Anthropogenic CO2 emissions have altered Earth’s climate system at an unprecedented rate, causing global climate change and ocean acidification. Surface ocean pH has increased by 26% since the industrial era and is predicted to increase another 100% by 2100. Additional stress from abrupt changes in carbonate chemistry in conjunction with other natural and anthropogenic impacts may push populations over critical thresholds. Bivalves are particularly vulnerable to the impacts of acidification during early life-history stages. Two substrate additives, shell hash and macrophytes, have been proposed as potential ocean acidification adaptation strategies for bivalves but there is limited research into their effectiveness. This study uses a split plot design to examine four different combinations of the two substratum treatments on juvenile Venerupis philippinarum settlement, survival, and growth and on local water chemistry at Fidalgo Bay and Skokomish Delta, Washington. -
Diversity of Norwegian Sea Slugs (Nudibranchia): New Species to Norwegian Coastal Waters and New Data on Distribution of Rare Species
Fauna norvegica 2013 Vol. 32: 45-52. ISSN: 1502-4873 Diversity of Norwegian sea slugs (Nudibranchia): new species to Norwegian coastal waters and new data on distribution of rare species Jussi Evertsen1 and Torkild Bakken1 Evertsen J, Bakken T. 2013. Diversity of Norwegian sea slugs (Nudibranchia): new species to Norwegian coastal waters and new data on distribution of rare species. Fauna norvegica 32: 45-52. A total of 5 nudibranch species are reported from the Norwegian coast for the first time (Doridoxa ingolfiana, Goniodoris castanea, Onchidoris sparsa, Eubranchus rupium and Proctonotus mucro- niferus). In addition 10 species that can be considered rare in Norwegian waters are presented with new information (Lophodoris danielsseni, Onchidoris depressa, Palio nothus, Tritonia griegi, Tritonia lineata, Hero formosa, Janolus cristatus, Cumanotus beaumonti, Berghia norvegica and Calma glau- coides), in some cases with considerable changes to their distribution. These new results present an update to our previous extensive investigation of the nudibranch fauna of the Norwegian coast from 2005, which now totals 87 species. An increase in several new species to the Norwegian fauna and new records of rare species, some with considerable updates, in relatively few years results mainly from sampling effort and contributions by specialists on samples from poorly sampled areas. doi: 10.5324/fn.v31i0.1576. Received: 2012-12-02. Accepted: 2012-12-20. Published on paper and online: 2013-02-13. Keywords: Nudibranchia, Gastropoda, taxonomy, biogeography 1. Museum of Natural History and Archaeology, Norwegian University of Science and Technology, NO-7491 Trondheim, Norway Corresponding author: Jussi Evertsen E-mail: [email protected] IntRODUCTION the main aims. -
Diarrhetic Shellfish Toxins and Other Lipophilic Toxins of Human Health Concern in Washington State
Mar. Drugs 2013, 11, 1-x manuscripts; doi:10.3390/md110x000x OPEN ACCESS Marine Drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Article Diarrhetic Shellfish Toxins and Other Lipophilic Toxins of Human Health Concern in Washington State Vera L. Trainer 1,*, Leslie Moore 1, Brian D. Bill 1, Nicolaus G. Adams 1, Neil Harrington 2, Jerry Borchert 3, Denis A.M. da Silva 1 and Bich-Thuy L. Eberhart 1 1 Marine Biotoxins Program, Environmental Conservation Division, Northwest Fisheries Science Center, National Marine Fisheries Service, National Oceanic and Atmospheric Administration, 2725 Montlake Blvd. E, Seattle, WA 98112, USA; E-Mails: [email protected] (L.M.); [email protected] (B.D.B.); [email protected] (N.G.A.); [email protected] (D.A.M.D.S.); [email protected] (B.-T.L.E.) 2 Jamestown S’Klallam Tribe, 1033 Old Blyn Highway, Sequim, WA 98392, USA; E-Mail: [email protected] 3 Office of Shellfish and Water Protection, Washington State Department of Health, 111 Israel Rd SE, Tumwater, WA 98504, USA; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +1-206-860-6788; Fax: +1-206-860-3335. Received: 13 March 2013; in revised form: 7 April 2013 / Accepted: 23 April 2013 / Published: Abstract: The illness of three people in 2011 after their ingestion of mussels collected from Sequim Bay State Park, Washington State, USA, demonstrated the need to monitor diarrhetic shellfish toxins (DSTs) in Washington State for the protection of human health. -
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. -
Review, the (Medical) Benefits and Disadvantage of Sea Cucumber
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN:2278-3008, p-ISSN:2319-7676. Volume 12, Issue 5 Ver. III (Sep. – Oct. 2017), PP 30-36 www.iosrjournals.org Review, The (medical) benefits and disadvantage of sea cucumber Leonie Sophia van den Hoek, 1) Emad K. Bayoumi 2). 1 Department of Marine Biology Science, Liberty International University, Wilmington, USA. Professional Member Marine Biological Association, UK. 2 Department of General Surgery, Medical Academy Named after S. I. Georgiesky of Crimea Federal University, Crimea, Russia Corresponding Author: Leonie Sophia van den Hoek Abstract: A remarkable feature of Holothurians is the catch collagen that forms their body wall. Catch collagen has two states, soft and stiff, that are under neurological control [1]. A study [3] provides evidence that the process of new organ formation in holothurians can be described as an intermediate process showing characteristics of both epimorphic and morphallactic phenomena. Tropical sea cucumbers, have a previously unappreciated role in the support of ecosystem resilience in the face of global change, it is an important consideration with respect to the bêche-de-mer trade to ensure sea cucumber populations are sustained in a future ocean [9]. Medical benefits of the sea cucumber are; Losing weight [19], decreasing cholesterol [10], improved calcium solubility under simulated gastrointestinal digestion and also promoted calcium absorption in Caco-2 and HT-29 cells [20], reducing arthritis pain [21], HIV therapy [21], treatment osteoarthritis [21], antifungal steroid glycoside [22], collagen protein [14], alternative to mammalian collagen [14], alternative for blood thinners [29], enhancing immunity and disease resistance [30]. -
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 ......................................................................... -
Physiological Adaptations and Feeding Mechanisms of the Invasive Purple Varnish Clam, Nuttallia Obscurata
Western Washington University Western CEDAR WWU Graduate School Collection WWU Graduate and Undergraduate Scholarship 2013 Physiological adaptations and feeding mechanisms of the invasive purple varnish clam, Nuttallia obscurata Leesa E. Sorber Western Washington University Follow this and additional works at: https://cedar.wwu.edu/wwuet Part of the Biology Commons Recommended Citation Sorber, Leesa E., "Physiological adaptations and feeding mechanisms of the invasive purple varnish clam, Nuttallia obscurata" (2013). WWU Graduate School Collection. 281. https://cedar.wwu.edu/wwuet/281 This Masters Thesis is brought to you for free and open access by the WWU Graduate and Undergraduate Scholarship at Western CEDAR. It has been accepted for inclusion in WWU Graduate School Collection by an authorized administrator of Western CEDAR. For more information, please contact [email protected]. PHYSIOLOGICAL ADAPTATIONS AND FEEDING MECHANISMS OF THE INVASIVE PURPLE VARNISH CLAM, NUTTALLIA OBSCURATA by Leesa E. Sorber Accepted in Partial Completion of the Requirements for the Degree Master of Science Kathleen L. Kitto, Dean of the Graduate School ADVISORY COMMITTEE Chair, Dr. Deborah Donovan Dr. Benjamin Miner Dr. Jose Serrano-Moreno MASTER’S THESIS In presenting this thesis in partial fulfillment of the requirements for a master’s degree at Western Washington University, I grant Western Washington University the non-exclusive royalty-free right to archive, reproduce, distribute, and display the thesis in any and all forms, including electronic format, via any digital library mechanisms maintained by WWU. I represent and warrant this is my original work, and does not infringe or violate any rights of others. I warrant that I have obtained written permission for the owner of any third party copyrighted material included in these files. -
List of Bivalve Molluscs from British Columbia, Canada
List of Bivalve Molluscs from British Columbia, Canada Compiled by Robert G. Forsyth Research Associate, Invertebrate Zoology, Royal BC Museum, 675 Belleville Street, Victoria, BC V8W 9W2; [email protected] Rick M. Harbo Research Associate, Invertebrate Zoology, Royal BC Museum, 675 Belleville Street, Victoria BC V8W 9W2; [email protected] Last revised: 11 October 2013 INTRODUCTION Classification rankings are constantly under debate and review. The higher classification utilized here follows Bieler et al. (2010). Another useful resource is the online World Register of Marine Species (WoRMS; Gofas 2013) where the traditional ranking of Pteriomorphia, Palaeoheterodonta and Heterodonta as subclasses is used. This list includes 237 bivalve species from marine and freshwater habitats of British Columbia, Canada. Marine species (206) are mostly derived from Coan et al. (2000) and Carlton (2007). Freshwater species (31) are from Clarke (1981). Common names of marine bivalves are from Coan et al. (2000), who adopted most names from Turgeon et al. (1998); common names of freshwater species are from Turgeon et al. (1998). Changes to names or additions to the fauna since these two publications are marked with footnotes. Marine groups are in black type, freshwater taxa are in blue. Introduced (non-indigenous) species are marked with an asterisk (*). Marine intertidal species (n=84) are noted with a dagger (†). Quayle (1960) published a BC Provincial Museum handbook, The Intertidal Bivalves of British Columbia. Harbo (1997; 2011) provided illustrations and descriptions of many of the bivalves found in British Columbia, including an identification guide for bivalve siphons and “shows”. Lamb & Hanby (2005) also illustrated many species. -
FAU Institutional Repository
FAU Institutional Repository http://purl.fcla.edu/fau/fauir This paper was submitted by the faculty of FAU’s Harbor Branch Oceanographic Institute. Notice: ©1989 Elsevier B.V. The final published version of this manuscript is available at http://www.sciencedirect.com/science/journal/00220981 and may be cited as: Cameron, J. L., & Fankboner, P. V. (1989). Reproductive biology of the commercial sea cucumber Parastichopus californicus (Stimpson) (Echinodermata: Holothuroidea). II. Observations on the ecology of development, recruitment and the juvenile life stage. Journal of Experimental Marine Biology and Ecology, 127(1), 43-67.doi:10.1016/0022-0981(89)90208-6 I i'V ) J. Exp. Mar. BioI. £Col., 1989, Vol. 127, pp. 43-67 43 Elsevier JEM 01229 Reproductive biology of the commercial sea cucumber Parastichopus californicus (Stimpson) (Echinodermata: Holothuroidea). II. Observations on the ecology of development, recruitment, and the juvenile life stage J. Lane Cameron and Peter V. Fankboner Department ofBiological Sciences. Simon Fraser University. Burnaby, British Columbia, Canada (Received 17 November 1987; revision received 9 January 1989; accepted 23 January 1989) Abstract: Evidence from in vitro culture of embryos and larvae of Parastichopus califomicus (Stimpson) suggests that asynchronization of development through metamorphosis and settlement results in a variable pelagic period for larvae within a particular cohort. Additionally, considerable variation in size of 0 + yr recruits observed in situ may indicate that settlement had occurred continuously for some months within the population studied. Recruitment of at least seven species of echinoderms (including P. californicus} was observed at distinct sites that were notably free of the predatory sea stars Solaster dawsoni (Verrill), S.