Species to Know Cnidaria and Ctenophora
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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. -
Metridium Farcimen (Tilesius, 1809)
RESEARCH ARTICLE Individual marking of soft-bodied subtidal invertebrates in situ ± A novel staining technique applied to the giant plumose anemone Metridium farcimen (Tilesius, 1809) Christopher D. Wells1,2*, Kenneth P. Sebens1,2,3 1 Biology Department, University of Washington, Seattle, WA, United States of America, 2 Friday Harbor a1111111111 Laboratories, University of Washington, Friday Harbor, WA, United States of America, 3 School of Aquatic and Fishery Sciences, University of Washington, Seattle, WA, United States of America a1111111111 a1111111111 * [email protected] a1111111111 a1111111111 Abstract The ability to recognize individuals and track growth over time is crucial to population OPEN ACCESS dynamics research as well as studies of animal behavior. Invertebrates are particularly diffi- cult to track as they often molt, have regenerative capabilities, or lack hard parts to attach Citation: Wells CD, Sebens KP (2017) Individual marking of soft-bodied subtidal invertebrates in markers. We tested, in laboratory and field studies, a new way of marking sea anemones situ ± A novel staining technique applied to the (order Actiniaria) by injection of three vital stains (i.e., neutral red, methylene blue, and fluo- giant plumose anemone Metridium farcimen rescein). Neutral red and methylene blue did not affect growth or survival, but fluorescein (Tilesius, 1809). PLoS ONE 12(11): e0188263. was lethal at high concentrations. Marked individuals could be identified up to seven months https://doi.org/10.1371/journal.pone.0188263 after injection -
Animal Origins and the Evolution of Body Plans 621
Animal Origins and the Evolution 32 of Body Plans In 1822, nearly forty years before Darwin wrote The Origin of Species, a French naturalist, Étienne Geoffroy Saint-Hilaire, was examining a lob- ster. He noticed that when he turned the lobster upside down and viewed it with its ventral surface up, its central nervous system was located above its digestive tract, which in turn was located above its heart—the same relative positions these systems have in mammals when viewed dorsally. His observations led Geoffroy to conclude that the differences between arthropods (such as lobsters) and vertebrates (such as mammals) could be explained if the embryos of one of those groups were inverted during development. Geoffroy’s suggestion was regarded as preposterous at the time and was largely dismissed until recently. However, the discovery of two genes that influence a sys- tem of extracellular signals involved in development has lent new support to Geof- froy’s seemingly outrageous hypothesis. Genes that Control Development A A vertebrate gene called chordin helps to establish cells on one side of the embryo human and a lobster carry similar genes that control the development of the body as dorsal and on the other as ventral. A probably homologous gene in fruit flies, called axis, but these genes position their body sog, acts in a similar manner, but has the opposite effect. Fly cells where sog is active systems inversely. A lobster’s nervous sys- become ventral, whereas vertebrate cells where chordin is active become dorsal. How- tem runs up its ventral (belly) surface, whereas a vertebrate’s runs down its dorsal ever, when sog mRNA is injected into an embryo (back) surface. -
Poster Final Copy
Introduction to Jellyfish Jellyfish have been around for over 700 million years making them one of the oldest living creatures on earth. There are almost 3,000 species of jellyfish found throughout the world's oceans. From Cnidarian jellyfish, which are often referred as “true” jellyfish, to Ctenophores (comb jellyfish), Cubic Aquarium Systems have compiled this poster showing some of the most interesting species found around the globe. Moon Jellyfish Amakusa Jellyfish Mauve Stinger Purple Striped Jellyfish Japanese Sea Nettle Aurelia aurita Sanderia malayensis Pelagia noctilca Chrysaora colorata Chrysaora pacifica Pacific Sea Nettle Black Sea Nettle Lion’s Mane Jellyfish Blue Fire Jellyfish Egg Yolk Jellyfish Chrysaora fuscescens Chrysaora achlyos Cyanea capillata Cyanea lamarckii Phacellophora camtschatica Flame Jellyfish Blue Blubber Spotted Lagoon Jellyfish Australian Spotted Lagoon Jellyfish Upside Down Jellyfish Rhopilema esculentum Catostylus mosaicus Mastigias papu Phyllorhiza punctata Cassioppea sp. Mediterranean Jellyfish Crown Jellyfish Purple Jellyfish Chrystal Jellyfish Flower Hat Jellyfish Cotylorhiza tuberculata Cephea cephea Thysanostoma thysanura Aequorea victoria Olindias formosa Immortal Jellyfish Portuguese Man O’ War Box Jellyfish Comb Jellyfish Sea Gooseberry Turritopsis dohrni Physalia physali Chironex sp. Bolinopsis sp. Pleurobrachia bachei Cubic Aquarium Systems Exotic Aquaculture Jellyfish aquariums and specialised fish tanks | Cubic Aquarium Syste International Jellyfish Wholesale Cubic Aquarium Systems build a range of unique, specialised aquariums Exotic Aquaculture are a Hong Kong based aquarium livestock supplier for jellyfish and other unusual sea creatures specializing in jellyfish wholesale to the public and home aquarium trade. www.cubicaquarium.com Copyright Sanderia Group Limited www.exoticaquaculture.com All rights reserved. -
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. -
John E. Morris Ally Described in 1860 As Sarcoptilus (Ptilosarcus) Gurneyi
AN ABSTRACT OF THE THESIS OF ROBERT EDWARD BATIEfor the MASTER OF SCIENCE (Name) (Degree) in Zoology presented on (Major) (Late) Title:TAXONOMY AND SOME ASPECTS OF THE BIOLOGY OF THE SEA PEN PTLLOSARCUS GURNEYI (CNIDARIA, PENNATULAC EA) Redacted for Privacy Abstract approved: Redacted for Privacy John E. Morris At present there is much confusion regarding the correct genus and species name for the shallow water, West coast sea pen.Origin- ally described in 1860 as Sarcoptilus (Ptilosarcus) gurneyi Gray, this sea pen has subsequently been placed inthree different genera, one of which has had three spelling variations, and in three different species groups under three spelling variations.Not only is there ex- tensive synonymy, but also homonymy exists between the generic names of a sea pen and a moth. The purpose of this investigation was to determine the valid taxonomic name and to supply more information about the sea pen with respect to its anatomy and biology. Sea pens were collected from Puget Sound, Washington, and from Monterey Bay, California,Their internal and external morpholo.- gies were compared; no detectable differences were found between the two populations, except in coloration.Coloration was not considered to be a stable enough character upon which tobase species differences. The taxonomic history of the West coast sea pen waspresented and reasons given for the subordination of the genusLeioptilus to the genus Ptilosarcus.Ptilosarcus gurneyi was recommended as the proper and valid binomen forthe shallow water sea pen with all other names being subordinated. Taxonomy and Some Aspects of the Biology of the Sea Pen Ptilosarcus gurn (Cnidaria, Pennatulacea) by Robert Edward Batie A THESIS submitted to Oregon State University in partial fulfillment of the requirements for the degree of Master of Science June 1971 APPROVED: Redacted for Privacy Dr. -
Bioluminescence and Fluorescence of Three Sea Pens in the North-West
bioRxiv preprint doi: https://doi.org/10.1101/2020.12.08.416396; this version posted December 9, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Bioluminescence and fluorescence of three sea pens in the north-west Mediterranean sea Warren R Francis* 1, Ana¨ısSire de Vilar 1 1: Dept of Biology, University of Southern Denmark, Odense, Denmark Corresponding author: [email protected] Abstract Bioluminescence of Mediterranean sea pens has been known for a long time, but basic parameters such as the emission spectra are unknown. Here we examined bioluminescence in three species of Pennatulacea, Pennatula rubra, Pteroeides griseum, and Veretillum cynomorium. Following dark adaptation, all three species could easily be stimulated to produce green light. All species were also fluorescent, with bioluminescence being produced at the same sites as the fluorescence. The shape of the fluorescence spectra indicates the presence of a GFP closely associated with light production, as seen in Renilla. Our videos show that light proceeds as waves along the colony from the point of stimulation for all three species, as observed in many other octocorals. Features of their bioluminescence are strongly suggestive of a \burglar alarm" function. Introduction Bioluminescence is the production of light by living organisms, and is extremely common in the marine environment [Haddock et al., 2010, Martini et al., 2019]. Within the phylum Cnidaria, biolumiescence is widely observed among the Medusazoa (true jellyfish and kin), but also among the Octocorallia, and especially the Pennatulacea (sea pens). -
Appendix C - Invertebrate Population Attributes
APPENDIX C - INVERTEBRATE POPULATION ATTRIBUTES C1. Taxonomic list of megabenthic invertebrate species collected C2. Percent area of megabenthic invertebrate species by subpopulation C3. Abundance of megabenthic invertebrate species by subpopulation C4. Biomass of megabenthic invertebrate species by subpopulation C- 1 C1. Taxonomic list of megabenthic invertebrate species collected on the southern California shelf and upper slope at depths of 2-476m, July-October 2003. Taxon/Species Author Common Name PORIFERA CALCEREA --SCYCETTIDA Amphoriscidae Leucilla nuttingi (Urban 1902) urn sponge HEXACTINELLIDA --HEXACTINOSA Aphrocallistidae Aphrocallistes vastus Schulze 1887 cloud sponge DEMOSPONGIAE Porifera sp SD2 "sponge" Porifera sp SD4 "sponge" Porifera sp SD5 "sponge" Porifera sp SD15 "sponge" Porifera sp SD16 "sponge" --SPIROPHORIDA Tetillidae Tetilla arb de Laubenfels 1930 gray puffball sponge --HADROMERIDA Suberitidae Suberites suberea (Johnson 1842) hermitcrab sponge Tethyidae Tethya californiana (= aurantium ) de Laubenfels 1932 orange ball sponge CNIDARIA HYDROZOA --ATHECATAE Tubulariidae Tubularia crocea (L. Agassiz 1862) pink-mouth hydroid --THECATAE Aglaopheniidae Aglaophenia sp "hydroid" Plumulariidae Plumularia sp "seabristle" Sertulariidae Abietinaria sp "hydroid" --SIPHONOPHORA Rhodaliidae Dromalia alexandri Bigelow 1911 sea dandelion ANTHOZOA --ALCYONACEA Clavulariidae Telesto californica Kükenthal 1913 "soft coral" Telesto nuttingi Kükenthal 1913 "anemone" Gorgoniidae Adelogorgia phyllosclera Bayer 1958 orange gorgonian Eugorgia -
Benthic Data Sheet
DEMERSAL OTTER/BEAM TRAWL DATA SHEET RESEARCH VESSEL_____________________(1/20/13 Version*) CLASS__________________;DATE_____________;NAME:___________________________; DEVICE DETAILS_________ LOCATION (OVERBOARD): LAT_______________________; LONG______________________________ LOCATION (AT DEPTH): LAT_______________________; LONG_____________________________; DEPTH___________ LOCATION (START UP): LAT_______________________; LONG______________________________;.DEPTH__________ LOCATION (ONBOARD): LAT_______________________; LONG______________________________ TIME: IN______AT DEPTH_______START UP_______SURFACE_______.DURATION OF TRAWL________; SHIP SPEED__________; WEATHER__________________; SEA STATE__________________; AIR TEMP______________ SURFACE TEMP__________; PHYS. OCE. NOTES______________________; NOTES_______________________________ INVERTEBRATES Phylum Porifera Order Pennatulacea (sea pens) Class Calcarea __________________________________ Family Stachyptilidae Class Demospongiae (Vase sponge) _________________ Stachyptilum superbum_____________________ Class Hexactinellida (Hyalospongia- glass sponge) Suborder Subsessiliflorae Subclass Hexasterophora Family Pennatulidae Order Hexactinosida Ptilosarcus gurneyi________________________ Family Aphrocallistidae Family Virgulariidae Aphrocallistes vastus ______________________ Acanthoptilum sp. ________________________ Other__________________________________________ Stylatula elongata_________________________ Phylum Cnidaria (Coelenterata) Virgularia sp.____________________________ Other_______________________________________ -
Ectosymbiotic Behavior of Cancer Gracilis and Its Trophic Relationships with Its Host Phacellophora Camtschatica and the Parasitoid Hyperia Medusarum
MARINE ECOLOGY PROGRESS SERIES Vol. 315: 221–236, 2006 Published June 13 Mar Ecol Prog Ser Ectosymbiotic behavior of Cancer gracilis and its trophic relationships with its host Phacellophora camtschatica and the parasitoid Hyperia medusarum Trisha Towanda*, Erik V. Thuesen Laboratory I, Evergreen State College, Olympia, Washington 98505, USA ABSTRACT: In southern Puget Sound, large numbers of megalopae and juveniles of the brachyuran crab Cancer gracilis and the hyperiid amphipod Hyperia medusarum were found riding the scypho- zoan Phacellophora camtschatica. C. gracilis megalopae numbered up to 326 individuals per medusa, instars reached 13 individuals per host and H. medusarum numbered up to 446 amphipods per host. Although C. gracilis megalopae and instars are not seen riding Aurelia labiata in the field, instars readily clung to A. labiata, as well as an artificial medusa, when confined in a planktonkreisel. In the laboratory, C. gracilis was observed to consume H. medusarum, P. camtschatica, Artemia franciscana and A. labiata. Crab fecal pellets contained mixed crustacean exoskeletons (70%), nematocysts (20%), and diatom frustules (8%). Nematocysts predominated in the fecal pellets of all stages and sexes of H. medusarum. In stable isotope studies, the δ13C and δ15N values for the megalopae (–19.9 and 11.4, respectively) fell closely in the range of those for H. medusarum (–19.6 and 12.5, respec- tively) and indicate a similar trophic reliance on the host. The broad range of δ13C (–25.2 to –19.6) and δ15N (10.9 to 17.5) values among crab instars reflects an increased diversity of diet as crabs develop. The association between C.