Island County/Wsu Beach Watchers
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GASTROPOD CARE SOP# = Moll3 PURPOSE: to Describe Methods Of
GASTROPOD CARE SOP# = Moll3 PURPOSE: To describe methods of care for gastropods. POLICY: To provide optimum care for all animals. RESPONSIBILITY: Collector and user of the animals. If these are not the same person, the user takes over responsibility of the animals as soon as the animals have arrived on station. IDENTIFICATION: Common Name Scientific Name Identifying Characteristics Blue topsnail Calliostoma - Whorls are sculptured spirally with alternating ligatum light ridges and pinkish-brown furrows - Height reaches a little more than 2cm and is a bit greater than the width -There is no opening in the base of the shell near its center (umbilicus) Purple-ringed Calliostoma - Alternating whorls of orange and fluorescent topsnail annulatum purple make for spectacular colouration - The apex is sharply pointed - The foot is bright orange - They are often found amongst hydroids which are one of their food sources - These snails are up to 4cm across Leafy Ceratostoma - Spiral ridges on shell hornmouth foliatum - Three lengthwise frills - Frills vary, but are generally discontinuous and look unfinished - They reach a length of about 8cm Rough keyhole Diodora aspera - Likely to be found in the intertidal region limpet - Have a single apical aperture to allow water to exit - Reach a length of about 5 cm Limpet Lottia sp - This genus covers quite a few species of limpets, at least 4 of them are commonly found near BMSC - Different Lottia species vary greatly in appearance - See Eugene N. Kozloff’s book, “Seashore Life of the Northern Pacific Coast” for in depth descriptions of individual species Limpet Tectura sp. - This genus covers quite a few species of limpets, at least 6 of them are commonly found near BMSC - Different Tectura species vary greatly in appearance - See Eugene N. -
Ascidian Cannibalism Correlates with Larval Behavior and Adult Distribution
FAU Institutional Repository http://purl.fcla.edu/fau/fauir This paper was submitted by the faculty of FAU’s Harbor Branch Oceanographic Institute. Notice: ©1988 Elsevier Ltd. The final published version of this manuscript is available at http://www.sciencedirect.com/science/journal/00220981 and may be cited as: Young, C. M. (1988). Ascidian cannibalism correlates with larval behavior and adult distribution. Journal of Experimental Marine Biology and Ecology, 117(1), 9-26. doi:10.1016/0022-0981(88)90068-8 J. Exp. Mar. Bioi. £Col., 1988, Vol. 117, pp. 9-26 9 Elsevier JEM 01042 Ascidian cannibalism correlates with larval behavior and adult distribution Craig M. Young Department ofLarval Ecology. Harbor Branch Oceanographic Institution, Fort Pierce, Florida. U.S.A. (Received 24 March 1987; revision received 9 December 1987; accepted 22 December 1987) Abstract: In the San Juan Islands, Washington, solitary ascidians .that occur in dense monospecific aggregations demonstrate gregarious settlement as larvae, whereas species that occur as isolated individuals do not. All gregarious species reject their own eggs and larvae as food, but nongregarious species consume conspecific eggs and larvae. Moreover, the rejection mechanism is species-specific in some cases. Correla tion analysis suggests that species specificity of the rejection response has a basis in siphon diameter, egg density, and larval size, but not in number of oral tentacles, or tentacle branching. One strongly cannibalistic species, Corella inflata Huntsman, avoids consuming its own eggs and newly released tadpoles by a unique brooding mechanism that involves floating eggs, negative geotaxis after hatching, and adult orientation. Key words: Ascidian; Cannibalism; Distribution; Larva; Settlement behavior INTRODUCTION Many sessile marine invertebrates, including filter-feeders such as mussels, oysters, barnacles and ascidians, occur in discrete, dense aggregations. -
MARINE TANK GUIDE About the Marine Tank
HOME EDITION MARINE TANK GUIDE About the Marine Tank With almost 34,000 miles of coastline, Alaska’s intertidal zones, the shore areas exposed and covered by ocean tides, are home to a variety of plants and animals. The Anchorage Museum’s marine tank is home to Alaskan animals which live in the intertidal zone. The plants and animals in the Museum’s marine tank are collected under an Alaska Department of Fish and Game Aquatic Resource Permit during low tide at various beaches in Southcentral and Southeast Alaska. Visitors are asked not to touch the marine animals. Touching is stressful for the animals. A full- time animal care technician maintains the marine tank. Since the tank is not located next to the ocean, ocean water cannot be constantly pumped through it. This means special salt water is mixed at the Museum. The tank is also cleaned regularly. Equipment which keeps the water moving, clean, chilled to 43°F and constantly monitored. Contamination from human hands would impact the cleanliness of the water and potentially hurt the animals. A second tank is home to the Museum’s king crab, named King Louie, and black rockfish, named Sebastian. King crab and black rockfish of Alaska live in deeper waters than the intertidal zone creatures. This guide shares information about some of the Museum’s marine animals. When known, the Dena’ina word for an animal is included, recognizing the thousands of years of stewardship and knowledge of Indigeneous people of the Anchorage area and their language. The Dena’ina & Marine Species The geographically diverse Dena’ina lands span both inland and coastal areas, including Anchorage. -
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. -
Black Oystercatcher Diet and Provisioning 2014 Annual Report
National Park Service U.S. Department of the Interior Natural Resource Stewardship and Science Black Oystercatcher Chick Diet and Provisioning 2014 Annual Report Natural Resource Data Series NPS/KEFJ/NRDS—2015/749 ON THIS PAGE Nest camera captures a black oystercatcher provisioning chick on Natoa Island. Photograph Courtesy: NPS/Kenai Fjords National Park ON THE COVER Black oystercatchers at nest in Aialik Bay, Kenai Fjords National Park Photograph by: NPS/Katie Thoresen Black Oystercatcher Diet and Provisioning 2014 Annual Report Natural Resource Data Series NPS/KEFJ/NRDS—2015/749 Sam Stark1, Brian Robinson2 and Laura M. Phillips1 1National Park Service Kenai Fjords National Park PO Box 1727 Seward, AK 99664 2 University of Alaska, Fairbanks Department of Biology and Wildlife PO Box 756100 Fairbanks, AK 99775 January 2015 U.S. Department of the Interior National Park Service Natural Resource Stewardship and Science Fort Collins, Colorado The National Park Service, Natural Resource Stewardship and Science office in Fort Collins, Colorado, publishes a range of reports that address natural resource topics. These reports are of interest and applicability to a broad audience in the National Park Service and others in natural resource management, including scientists, conservation and environmental constituencies, and the public. The Natural Resource Data Series is intended for the timely release of basic data sets and data summaries. Care has been taken to assure accuracy of raw data values, but a thorough analysis and interpretation of the data has not been completed. Consequently, the initial analyses of data in this report are provisional and subject to change. All manuscripts in the series receive the appropriate level of peer review to ensure that the information is scientifically credible, technically accurate, appropriately written for the intended audience, and designed and published in a professional manner. -
Biodiversity Journal, 2021, 12 (1): 225–228
Biodiversity Journal, 2021, 12 (1): 225–228 https://doi.org/10.31396/Biodiv.Jour.2021.12.4.225.228 First record of Calliostoma lusitanicum F. Nordsieck et García- Talavera, 1979 (Gastropoda Calliostomatiidae) in the Mediter- ranean Sea and remarks on C. alexandrinum Pallary, 1912 Andrea Nappo1*, Daniel Pellegrini2 & Attilio Pagli3 1Via S’Arrulloni 25, 09045 Quartu Sant’Elena, Cagliari, Italy; e-mail: [email protected] 2Via Colle Morello 2, 00038 Valmontone, Roma, Italy; e-mail: [email protected] 3Via Valdorme 55, 50053 Empoli, Firenze, Italy; e-mail: [email protected] *Corresponding author ABSTRACT In this work is reported for the first time the presence of Calliostoma lusitanicum F. Nordsieck et García-Talavera, 1979 (Gastropoda Calliostomatiidae) in the Mediterranean Sea. Present sightings widen the known distribution of this species, found in the Madeira Archipelago and Canary Islands. The relationship between C. lusitanicum and C. alexandrinum Pallary, 1912 is discussed. KEY WORDS Calliostoma lusitanicum; Calliostomatiidae; Mollusca; Mediterranean Sea. Received 08.11.2020; accepted 26.02.2021; published online 15.03.2021 INTRODUCTION as shell height. Photos are obtained with a Nikon D90 and processed with Adobe Photoshop CC®. According to WoRMS (accessed on ABBREVIATIONS AND ACRONYMS. The 14.10.2020), 291 re cent species are currently placed following abbreviations and acronyms are used: in the genus Calliostoma Swainson, 1840 (Gas- AN: Andrea Nappo collection (Quartu Sant’Elena, tropoda Calliostomatiidae) with a worldwide distri- Cagliari, Italy); AP: Attilio Pagli collection (Em- bution. In the Medi terranean Sea, according to the poli, Firenze, Italy); DP: Daniel Pellegrini collec- systematic list of the SIM (Italian Society of Mala- tion (Valmontone, Roma, Italy); MNHN: Muséum cology) (accessed 14.10.2020), 11 species are pres- National d’Histoire Naturelle (Paris, France); SIM: ent. -
Skye: a Landscape Fashioned by Geology
SCOTTISH NATURAL SKYE HERITAGE A LANDSCAPE FASHIONED BY GEOLOGY SKYE A LANDSCAPE FASHIONED BY GEOLOGY SCOTTISH NATURAL HERITAGE Scottish Natural Heritage 2006 ISBN 1 85397 026 3 A CIP record is held at the British Library Acknowledgements Authors: David Stephenson, Jon Merritt, BGS Series editor: Alan McKirdy, SNH. Photography BGS 7, 8 bottom, 10 top left, 10 bottom right, 15 right, 17 top right,19 bottom right, C.H. Emeleus 12 bottom, L. Gill/SNH 4, 6 bottom, 11 bottom, 12 top left, 18, J.G. Hudson 9 top left, 9 top right, back cover P&A Macdonald 12 top right, A.A. McMillan 14 middle, 15 left, 19 bottom left, J.W.Merritt 6 top, 11 top, 16, 17 top left, 17 bottom, 17 middle, 19 top, S. Robertson 8 top, I. Sarjeant 9 bottom, D.Stephenson front cover, 5, 14 top, 14 bottom. Photographs by Photographic Unit, BGS Edinburgh may be purchased from Murchison House. Diagrams and other information on glacial and post-glacial features are reproduced from published work by C.K. Ballantyne (p18), D.I. Benn (p16), J.J. Lowe and M.J.C. Walker. Further copies of this booklet and other publications can be obtained from: The Publications Section, Cover image: Scottish Natural Heritage, Pinnacle Ridge, Sgurr Nan Gillean, Cullin; gabbro carved by glaciers. Battleby, Redgorton, Perth PH1 3EW Back page image: Tel: 01783 444177 Fax: 01783 827411 Cannonball concretions in Mid Jurassic age sandstone, Valtos. SKYE A Landscape Fashioned by Geology by David Stephenson and Jon Merritt Trotternish from the south; trap landscape due to lavas dipping gently to the west Contents 1. -
Calcification of the Arctic Coralline Red Algae Lithothamnion Glaciale in Response to Elevated CO2
Vol. 441: 79–87, 2011 MARINE ECOLOGY PROGRESS SERIES Published November 15 doi: 10.3354/meps09405 Mar Ecol Prog Ser OPENPEN ACCESSCCESS Calcification of the Arctic coralline red algae Lithothamnion glaciale in response to elevated CO2 Jan Büdenbender*, Ulf Riebesell, Armin Form Leibniz Institute of Marine Sciences (IFM-GEOMAR), University of Kiel, Düsternbrooker Weg 20, 24105 Kiel, Germany ABSTRACT: Rising atmospheric CO2 concentrations could cause a calcium carbonate subsatura- tion of Arctic surface waters in the next 20 yr, making these waters corrosive for calcareous organ- isms. It is presently unknown what effects this will have on Arctic calcifying organisms and the ecosystems of which they are integral components. So far, acidification effects on crustose coralline red algae (CCA) have only been studied in tropical and Mediterranean species. In this work, we investigated calcification rates of the CCA Lithothamnion glaciale collected in northwest Svalbard in laboratory experiments under future atmospheric CO2 concentrations. The algae were exposed to simulated Arctic summer and winter light conditions in 2 separate experiments at opti- mum growth temperatures. We found a significant negative effect of increased CO2 levels on the net calcification rates of L. glaciale in both experiments. Annual mean net dissolution of L. glaciale was estimated to start at an aragonite saturation state between 1.1 and 0.9 which is projected to occur in parts of the Arctic surface ocean between 2030 and 2050 if emissions follow ‘business as usual’ scenarios (SRES A2; IPCC 2007). The massive skeleton of CCA, which consist of more than 80% calcium carbonate, is considered crucial to withstanding natural stresses such as water move- ment, overgrowth or grazing. -
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: ©1984 Elsevier B.V. This manuscript is an author version with the final publication available at http://www.sciencedirect.com/science/journal/00220981 and may be cited as: Wilson, W. H., Jr. (1984). Non‐overlapping distributions of spionid polychaetes: the relative importance of habitat and competition. Journal of Experimental Marine Biology and Ecology, 75(2), 119‐127. doi:10.1016/0022‐0981(84)90176‐X J. Exp. Mar. Bioi. Ecol., 1984, Vol. 75, pp. 119-127 119 Elsevier JEM 217 NON-OVERLAPPING DISTRIBUTIONS OF SPIONID POLYCHAETES: THE RELATIVE IMPORTANCE OF HABITAT AND COMPETITIONI W. HERBERT WILSON, JR. Harbor Branch Institution, Inc .. R.R. 1, Box 196, Fort Pierce, FL 33450. U.S.A. Abstract: The spionid polychaetes, Pygospio elegans Claparede, Pseudopolydora kempi (Southern), and Rhynchospio arenincola Hartman are found in False Bay, Washington. Two species, Pygospio elegans and Pseudopolydora kempi, co-occur in the high intertidal zone. The third species Rhynchospio arenincola occurs only in low intertidal areas. Reciprocal transplant experiments were used to test the importance of intraspecific density, interspecific density, and habitat on the survivorship of experimental animals. For all three species, only habitat had a significant effect. Individuals of each species survived better in experimental containers in their native habitat, regardless of the heterospecific and conspecific densities used in the experiments. The physical stresses associated with the prolonged exposure of the high intertidal site are experimentally shown to result in Rhynchospio mortality. From these experiments, habitat type is the only significant factor tested which can explain the observed distributions; the presence of confamilials has no detected effect on the survivorship of any species, suggesting that competition does not serve to maintain the patterns of distribution. -
554 Journal of Paleontology, V. 66, No. 4, 1992 Figure 9
554 JOURNAL OF PALEONTOLOGY, V. 66, NO. 4, 1992 FIGURE 9—Crepidula adunca encrusting living Calliostoma ligatum, Friday Harbor, Washington, shell height of C. ligatum, 21.0 mm, UCMP Type No. 39688. 1, two C. adunca conforming to upper whorls of C. ligatum; 2, C. adunca permanent scar on last whorl of hermitted C. ligatum, shell height, 22.0 mm, UCMP Type No. 39689. 1979). Other species also compete for, or inhabit, gastropod (Hyden and Forest, 1980). However, the shell-encrusting and shells (McLean, 1983; Vermeij, 1987; Walker, 1990). Because boring organisms that occur with hermit crabs have a long fossil empty shells may be rare, post-Triassic gastropod fossil assem- record, dating from the middle Jurassic. Determining the extent blages have most likely been taphonomically affected by sec- of hermitted shells in fossil assemblages should be the first line ondary occupants of shells. Because hermit crab modification of inquiry before paleoecological or evolutionary assessments of gastropod assemblages is great, Shimoyama et al. (1979) sug- are made. gested that the bivalve fossil record provided a more accurate Pagurized shells can be recognized by the settlement of bionts paleoecological record than gastropod assemblages. However, in specific locations on fossil shells (Palmer and Hancock, 1973; gastropod fossil assemblages provide valuable paleoecological Walker, 1988b, 1989, this paper). Recent and fossil biont pat- information for the history of the hermit crab. terns appear to be conservative from the Oligocene to the pres- Hermit crab body fossils are rare. Therefore, it is important ent. That is, taphonomically preserved biont patterns (e.g., east to study their other fossil record: that of the epi- and endobionts Gulf Coast examples) are similar to Recent pagurized shells. -
Appendix 3 Marine Spcies Lists
Appendix 3 Marine Species Lists with Abundance and Habitat Notes for Provincial Helliwell Park Marine Species at “Wall” at Flora Islet and Reef Marine Species at Norris Rocks Marine Species at Toby Islet Reef Marine Species at Maude Reef, Lambert Channel Habitats and Notes of Marine Species of Helliwell Provincial Park Helliwell Provincial Park Ecosystem Based Plan – March 2001 Marine Species at wall at Flora Islet and Reef Common Name Latin Name Abundance Notes Sponges Cloud sponge Aphrocallistes vastus Abundant, only local site occurance Numerous, only local site where Chimney sponge, Boot sponge Rhabdocalyptus dawsoni numerous Numerous, only local site where Chimney sponge, Boot sponge Staurocalyptus dowlingi numerous Scallop sponges Myxilla, Mycale Orange ball sponge Tethya californiana Fairly numerous Aggregated vase sponge Polymastia pacifica One sighting Hydroids Sea Fir Abietinaria sp. Corals Orange sea pen Ptilosarcus gurneyi Numerous Orange cup coral Balanophyllia elegans Abundant Zoanthids Epizoanthus scotinus Numerous Anemones Short plumose anemone Metridium senile Fairly numerous Giant plumose anemone Metridium gigantium Fairly numerous Aggregate green anemone Anthopleura elegantissima Abundant Tube-dwelling anemone Pachycerianthus fimbriatus Abundant Fairly numerous, only local site other Crimson anemone Cribrinopsis fernaldi than Toby Islet Swimming anemone Stomphia sp. Fairly numerous Jellyfish Water jellyfish Aequoria victoria Moon jellyfish Aurelia aurita Lion's mane jellyfish Cyanea capillata Particuilarly abundant -
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.