Tracking Temporal and Seasonal Changes in Nudibranch Populations: Citizen Science Data from a Community Aquarium
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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 -
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. -
Nudibranchs—Splendid Sea Slugs
Nudibranchs—Splendid Sea Slugs View the video “Nudibranchs” to learn about the adaptations of nudibranchs—colorful sea slugs with a remarkable means of defense. SUBJECT NUDIBRANCHS Science Watch it online at http://www.pbs.org/kqed/oceanadventures/video/nudibranchs GRADE LEVEL 5–10 Video length: 1 minute 52 seconds STANDARDS National Science Education BACKGROUND INFORMATION Standards Nudibranchs are sea slugs. They are soft-bodied animals, and like Grades 5–8 clams, snails and squid, they are mollusks. Nudibranchs belong to www.nap.edu/readingroom/books/ phylum Mollusca, class Gastropoda, order Nudibranchia. Found nses/6d.html#ls in oceans all over the world, they range in size from .25 inch to longer than a foot. There are more than 3,000 known species of Life Science – nudibranchs, and they come in all colors, from bright blue to pink Content Standard C: to white with orange polka dots. Regulation and Behavior Diversity and Adaptations Nudibranchs get their name from the feathery gills exposed on their of Organisms backs. The word nudibranch actually means “naked gills.” The two Ocean Literacy Essential most common groups of nudibranchs are the dorids and aeolids. Principles and Fundamental Dorids have a circular tuft of gills on their back that can be withdrawn Concepts: into their body. Aeolids have fingerlike projections, called cerata, www.coexploration.org/ that function as gills and are always exposed. Cerata also contain oceanliteracy/ branches of the digestive tract. Essential Principle #5: To find food, nudibranchs use their rhinophores—organs that sense The ocean supports a great chemical signals in the water. Most dorid nudibranchs feed on diversity of life and ecosystems. -
A Radical Solution: the Phylogeny of the Nudibranch Family Fionidae
RESEARCH ARTICLE A Radical Solution: The Phylogeny of the Nudibranch Family Fionidae Kristen Cella1, Leila Carmona2*, Irina Ekimova3,4, Anton Chichvarkhin3,5, Dimitry Schepetov6, Terrence M. Gosliner1 1 Department of Invertebrate Zoology, California Academy of Sciences, San Francisco, California, United States of America, 2 Department of Marine Sciences, University of Gothenburg, Gothenburg, Sweden, 3 Far Eastern Federal University, Vladivostok, Russia, 4 Biological Faculty, Moscow State University, Moscow, Russia, 5 A.V. Zhirmunsky Instutute of Marine Biology, Russian Academy of Sciences, Vladivostok, Russia, 6 National Research University Higher School of Economics, Moscow, Russia a11111 * [email protected] Abstract Tergipedidae represents a diverse and successful group of aeolid nudibranchs, with approx- imately 200 species distributed throughout most marine ecosystems and spanning all bio- OPEN ACCESS geographical regions of the oceans. However, the systematics of this family remains poorly Citation: Cella K, Carmona L, Ekimova I, understood since no modern phylogenetic study has been undertaken to support any of the Chichvarkhin A, Schepetov D, Gosliner TM (2016) A Radical Solution: The Phylogeny of the proposed classifications. The present study is the first molecular phylogeny of Tergipedidae Nudibranch Family Fionidae. PLoS ONE 11(12): based on partial sequences of two mitochondrial (COI and 16S) genes and one nuclear e0167800. doi:10.1371/journal.pone.0167800 gene (H3). Maximum likelihood, maximum parsimony and Bayesian analysis were con- Editor: Geerat J. Vermeij, University of California, ducted in order to elucidate the systematics of this family. Our results do not recover the tra- UNITED STATES ditional Tergipedidae as monophyletic, since it belongs to a larger clade that includes the Received: July 7, 2016 families Eubranchidae, Fionidae and Calmidae. -
Marine Invertebrate Field Guide
Marine Invertebrate Field Guide Contents ANEMONES ....................................................................................................................................................................................... 2 AGGREGATING ANEMONE (ANTHOPLEURA ELEGANTISSIMA) ............................................................................................................................... 2 BROODING ANEMONE (EPIACTIS PROLIFERA) ................................................................................................................................................... 2 CHRISTMAS ANEMONE (URTICINA CRASSICORNIS) ............................................................................................................................................ 3 PLUMOSE ANEMONE (METRIDIUM SENILE) ..................................................................................................................................................... 3 BARNACLES ....................................................................................................................................................................................... 4 ACORN BARNACLE (BALANUS GLANDULA) ....................................................................................................................................................... 4 HAYSTACK BARNACLE (SEMIBALANUS CARIOSUS) .............................................................................................................................................. 4 CHITONS ........................................................................................................................................................................................... -
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. -
Point Lobos Nudibranch Project Topics for Tonight
Point Lobos Nudibranch Project Topics for Tonight • Project Design, Location and Transect Selection • Nudibranch Identification • Species in the Study • Look-alikes • Sampling Techniques and Data Sheets • Q & A Project Design • Project Design, Location and Transect Selection • Science goals are still being defined. • Hope is to maximize the value of any data we collect. • Cover a variety of species and habitats. • Ease of study was also important. • Sites need to be near each other to maximize data collection time. • Sites need to be easy to find. • Transects need to be easy identify for repeatability. • Species covered need to be common and diverse. Locations • We have chosen two areas for study. • The North end of the Middle Reef • The North end of the Hole-in-the-wall Reef • Each reef will be divided into 4 transect zones. • East Wall • North Wall • West Wall • Top (defined as anything with less than 45 degrees of slope. • Actual transect areas are TBD and will need to be surveyed. • Each transect area needs to be roughly the same size • Transects must be easily identifiable. Locations Rationale • Middle Reef and Hole-in-the-wall Reefs are easily locatable underwater. • Both sites have good populations of nudibranchs. • Both sites have diverse habitat areas. • Hole-in-the-wall Reef may be lacking in “top” and North areas. • A survey will help here. • We’re open to other suggestions. Species in the Study • We have 14 species in the study. • All are at least reasonably common in Whaler’s Cove. • They represent a wide variety of species and prey items. -
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. -
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 ......................................................................... -
NIH Public Access Author Manuscript Toxicon
NIH Public Access Author Manuscript Toxicon. Author manuscript; available in PMC 2010 December 15. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Toxicon. 2009 December 15; 54(8): 1065±1070. doi:10.1016/j.toxicon.2009.02.029. Acquisition and Use of Nematocysts by Cnidarian Predators Paul G. Greenwood Department of Biology, Colby College, Waterville, ME 04901, USA, [email protected] Abstract Although toxic, physically destructive, and produced solely by cnidarians, cnidocysts are acquired, stored, and used by some predators of cnidarians. Despite knowledge of this phenomenon for well over a century, little empirical evidence details the mechanisms of how (and even why) these organisms use organelles of cnidarians. However, in the past twenty years a number of published experimental investigations address two of the fundamental questions of nematocyst acquisition and use by cnidarian predators: 1) how are cnidarian predators protected from cnidocyst discharge during feeding, and 2) how are the nematocysts used by the predator? Keywords Nudibranch; Nematocyst; Kleptocnidae; Cerata; Cnidocyst; Venom; Cnidaria Introduction Nematocysts, cnidocysts used to inject venom, offer a formidable defense from predators, but despite this weaponry numerous animals from many phyla prey on cnidarians (Salvini-Plawen, 1972; Ates, 1989, 1991; Arai, 2005). Some of these predators acquire unfired cnidocysts from their prey and store those cnidocysts in functional form within their own cells; the acquired cnidocysts (which are always nematocysts) are referred to as kleptocnidae. While aeolid nudibranchs are known for sequestering nematocysts from their prey (reviewed in Greenwood, 1988), one ctenophore species, Haeckelia rubra, preys upon narcomedusae and incorporates nematocysts into its own tentacles (Carré and Carré, 1980; Mills and Miller, 1984; Carré et al., 1989). -
Trivialnamen Für Mollusken Des Meeres Und Brackwassers in Deutschland (Polyplacophora, Gastropoda, Bivalvia, Scaphopoda Et Cephalopoda)
> Mollusca 27 (1) 2009 3 3 – 32 © Museum für Tierkunde Dresden, ISSN 1864-5127, 15.04.2009 Trivialnamen für Mollusken des Meeres und Brackwassers in Deutschland (Polyplacophora, Gastropoda, Bivalvia, Scaphopoda et Cephalopoda) FRITZ GOSSELCK 1, ALEXANDER DARR 1, JÜRGEN H. JUNGBLUTH 2 & MICHAEL L. ZETTLER 3 1 Institut für Angewandte Ökologie GmbH, Alte Dorfstraße 11, D-18184 Broderstorf, Germany [email protected] 2 In der Aue 30e, D-69118 Schlierbach, Germany PROJEKTGRUPPE MOLLUSKENKARTIERUNG © [email protected] 3 Leibniz-Institut für Ostseeforschung Warnemünde, Seestraße 15, D-18119 Rostock, Germany [email protected] Received on July 11, 2008, accepted on February 10, 2009. Published online at www.mollusca-journal.de > Abstract German common names for marine and brackish water molluscs. – A list of common names of German marine and brackish water molluscs was compiled for the German coastal waters and the exclusive economic zone (EEZ) of the North and Baltic Seas. Main aim of this compilation is to give interested non-professionals better access to and understanding of sea shells and squids. As often long-lived and relatively stationary species, molluscs can provide a key function as water quality indicators. The taxonomic classifi cation was based on the Mollusca databases CLEMAM and ERMS (MARBEF). The list includes 309 species. > Kurzfassung Eine Liste deutscher Namen der marinen und Brackwasser-Mollusken der deutschen Küstengewässer und der Ausschließlichen Wirtschaftszone (AWZ) der Nord- und Ostsee wurde erstellt. Ziel der Zusammenstellung ist es, mit den Trivialnamen dem interessierten Laien die marinen Schnecken, Muscheln und Tintenfi sche etwas näher zu bringen. -
The Extraordinary Genus Myja Is Not a Tergipedid, but Related to the Facelinidae S
A peer-reviewed open-access journal ZooKeys 818: 89–116 (2019)The extraordinary genusMyja is not a tergipedid, but related to... 89 doi: 10.3897/zookeys.818.30477 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s. str. with the addition of two new species from Japan (Mollusca, Nudibranchia) Alexander Martynov1, Rahul Mehrotra2,3, Suchana Chavanich2,4, Rie Nakano5, Sho Kashio6, Kennet Lundin7,8, Bernard Picton9,10, Tatiana Korshunova1,11 1 Zoological Museum, Moscow State University, Bolshaya Nikitskaya Str. 6, 125009 Moscow, Russia 2 Reef Biology Research Group, Department of Marine Science, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand 3 New Heaven Reef Conservation Program, 48 Moo 3, Koh Tao, Suratthani 84360, Thailand 4 Center for Marine Biotechnology, Department of Marine Science, Faculty of Science, Chulalongkorn Univer- sity, Bangkok 10330, Thailand5 Kuroshio Biological Research Foundation, 560-I, Nishidomari, Otsuki, Hata- Gun, Kochi, 788-0333, Japan 6 Natural History Museum, Kishiwada City, 6-5 Sakaimachi, Kishiwada, Osaka Prefecture 596-0072, Japan 7 Gothenburg Natural History Museum, Box 7283, S-40235, Gothenburg, Sweden 8 Gothenburg Global Biodiversity Centre, Box 461, S-40530, Gothenburg, Sweden 9 National Mu- seums Northern Ireland, Holywood, Northern Ireland, UK 10 Queen’s University, Belfast, Northern Ireland, UK 11 Koltzov Institute of Developmental Biology RAS, 26 Vavilova Str., 119334 Moscow, Russia Corresponding author: Alexander Martynov ([email protected]) Academic editor: Nathalie Yonow | Received 10 October 2018 | Accepted 3 January 2019 | Published 23 January 2019 http://zoobank.org/85650B90-B4DD-4FE0-8C16-FD34BA805C07 Citation: Martynov A, Mehrotra R, Chavanich S, Nakano R, Kashio S, Lundin K, Picton B, Korshunova T (2019) The extraordinary genus Myja is not a tergipedid, but related to the Facelinidae s.