Velutina Velutina ((OF Müller, 1776), )

Total Page:16

File Type:pdf, Size:1020Kb

Velutina Velutina ((OF Müller, 1776), ) Arctic Megabenthos Velutina velutina ((O. F. Müller, 1776), ) Phylum: Mollusca Class: Gastropoda Order: Littorinimorpha Family: Velutinidae Genus: Velutina Synonyms: Velutina laevigata (O. F. Müller, 1777), Velutina laevigata (Linnaeus, 1758) Description. - Shell with 3 convex rounded whorls, deeply impressed suture and well developed calcareous layer and periostracum. Upper part of spire projects slightly above inflated last whorl which occupies almost entire shell. Protoconch small, white, uncovered by periostracum. Periostracum fibrous, yellowish or brown, tightly adherent to shell forming closely spaced discontinuous spiral crests. Intervals between crests are equal to or 2 times the crest thickness. Adult individuals with 22-30 crests on last whorl. Sculpture on calcareous layer of ir¬regular growth lines crossing spiral riblets. The ribs correspond to crests on per¬iostracum. Aperture broad, almost rounded, opaque-white on inside. Inner lip slightly turned back on outside. Measurements. - Largest seen specimen: height 15 mm, length 26 mm, width 20 mm. Remarks. - The species is separated from the closely related V. (V.) schneideri by a more strongly developed periostracum structure with 22-30 spiral crests on last whorl. Distribution. - In the Arctic Region the species is circumpolar. In the Pacific it occurs in the Bering and northern parts of Okhotsk and Japan Seas as well as Gulf of Alaska. In accordance with MacGinitie (1959), the species is found in Monterey Bay (California) and in the Atlantic Ocean it is distributed to Cape Hatteras and Portugal. Ecology. - The species occurs at depths from 0.5 to 408 m, most common at 20 to 150 m on mud, gravel and pebble mixture and muddy sand substrata, often in Laminaria and other algae as well as on ascidians. Literature ● Gulbin V.V., Golikov A.N. A review of the prosobranch family Velutinidae in cold and temperate waters of the Northern Hemisphere. III. Velutininae. Genera Ciliatovelutina and Velutina Pic. 1 Pic. 2 Author: Zakharov Denis V. / 12.02.2017 Last edit: Zakharov Denis V. / 07.03.2017.
Recommended publications
  • Vespa Velutina (10 Años D’Una Invasión En Volanderes)
    Otru vecín peligrosu ya imposible de desaniciar n’Asturies: Vespa velutina (10 años d’una invasión en volanderes) Por Andrés Arias Rodríguez Departamentu de Bioloxía d’ Organismos y Sistemes (Zooloxía) Universidá d’Uviéu Vespa velutina nuna flor deCallistemon citrinus /50/ Ciencies 10 (2020) (2020) Ciencies 10 /51/ / Otru vecín peligrosu ya imposible de desaniciar n’Asturies: Vespa velutina (10 años d’una invasión en volanderes) ANTECEDENTES Vespa velutina ye una de les 22 especies del xéneru Vespa güei aceutaes. Vespa velutina Lepeletier, 1836 ye una espe- cómo la falta d’implicación político-social dio Presenta 10-12 variaciones nel so patrón de coloración, que vienen cie d’aviespa d’orixe asiáticu que pertenez a la nun problema d’ámbitu européu que requier considerándose como subespecies o variedaes xeográques, magar que pa familia Vespidae conocida comúnmente como l’establecimientu de polítiques urxentes y ama- «aviespa o tártagu asiáticu» o «aviespa de pa- ñoses, non solo pa controlar esta problemática dellos autores son simplemente morfos o variedaes de color. La subespecie tes marielles». Esta especie introdúxose de for- sinón pa evitar problemes futuros con otres es- introducida n’Europa ye V. velutina nigrithorax du Buysson, 1905 ma accidental n’Europa al rodiu del añu 2004, pecies exótiques invasores. N’España, l’aviespa deteutándose per primer vez nel llugar de Lot- asiática ta considerada ocialmente como una et-Garonne en Francia (Haxaire et al., 2006; especie invasora y apaez nel Catálogu Español Villemant et al., 2006). De magar s’introduxere d’Especies Exótiques Invasores (Real Decretu DERECHA en Francia, foi pa colonizar rápidamente otros 630/2013, de 2 d’agostu, pel que se regula esti Figura 1.
    [Show full text]
  • Habitat Usage by the Page Springsnail, Pyrgulopsis Morrisoni (Gastropoda: Hydrobiidae), from Central Arizona
    THE VELIGER ᭧ CMS, Inc., 2006 The Veliger 48(1):8–16 (June 30, 2006) Habitat Usage by the Page Springsnail, Pyrgulopsis morrisoni (Gastropoda: Hydrobiidae), from Central Arizona MICHAEL A. MARTINEZ* U.S. Fish and Wildlife Service, 2321 W. Royal Palm Rd., Suite 103, Phoenix, Arizona 85021, USA (*Correspondent: mike࿞[email protected]) AND DARRIN M. THOME U.S. Fish and Wildlife Service, 2800 Cottage Way, Rm. W-2605, Sacramento, California 95825, USA Abstract. We measured habitat variables and the occurrence and density of the Page springsnail, Pyrgulopsis mor- risoni (Hershler & Landye, 1988), in the Oak Creek Springs Complex of central Arizona during the spring and summer of 2001. Occurrence and high density of P. morrisoni were associated with gravel and pebble substrates, and absence and low density with silt and sand. Occurrence and high density were also associated with lower levels of dissolved oxygen and low conductivity. Occurrence was further associated with shallower water depths. Water velocity may play an important role in maintaining springsnail habitat by influencing substrate composition and other physico-chemical variables. Our study constitutes the first empirical effort to define P. morrisoni habitat and should be useful in assessing the relative suitability of spring environments for the species. The best approach to manage springsnail habitat is to maintain springs in their natural state. INTRODUCTION & Landye, 1988), is medium-sized relative to other con- geners, 1.8 to 2.9 mm in shell height, endemic to the The role that physico-chemical habitat variables play in Upper Verde River drainage of central Arizona (Williams determining the occurrence and density of aquatic micro- et al., 1985; Hershler & Landye, 1988; Hershler, 1994), invertebrates in spring ecosystems has been poorly stud- with all known populations existing within a complex of ied.
    [Show full text]
  • Rachor, E., Bönsch, R., Boos, K., Gosselck, F., Grotjahn, M., Günther, C
    Rachor, E., Bönsch, R., Boos, K., Gosselck, F., Grotjahn, M., Günther, C.-P., Gusky, M., Gutow, L., Heiber, W., Jantschik, P., Krieg, H.J., Krone, R., Nehmer, P., Reichert, K., Reiss, H., Schröder, A., Witt, J. & Zettler, M.L. (2013): Rote Liste und Artenlisten der bodenlebenden wirbellosen Meerestiere. – In: Becker, N.; Haupt, H.; Hofbauer, N.; Ludwig, G. & Nehring, S. (Red.): Rote Liste gefährdeter Tiere, Pflanzen und Pilze Deutschlands, Band 2: Meeresorganismen. – Münster (Landwirtschaftsverlag). – Na- turschutz und Biologische Vielfalt 70 (2): S. 81-176. Die Rote Liste gefährdeter Tiere, Pflanzen und Pilze Deutschlands, Band 2: Meeres- organismen (ISBN 978-3-7843-5330-2) ist zu beziehen über BfN-Schriftenvertrieb – Leserservice – im Landwirtschaftsverlag GmbH 48084 Münster Tel.: 02501/801-300 Fax: 02501/801-351 http://www.buchweltshop.de/bundesamt-fuer-naturschutz.html bzw. direkt über: http://www.buchweltshop.de/nabiv-heft-70-2-rote-liste-gefahrdeter-tiere-pflanzen-und- pilze-deutschlands-bd-2-meeresorganismen.html Preis: 39,95 € Naturschutz und Biologische Vielfalt 70 (2) 2013 81 –176 Bundesamtfür Naturschutz Rote Liste und Artenlisten der bodenlebenden wirbellosen Meerestiere 4. Fassung, Stand Dezember 2007, einzelne Aktualisierungenbis 2012 EIKE RACHOR,REGINE BÖNSCH,KARIN BOOS, FRITZ GOSSELCK, MICHAEL GROTJAHN, CARMEN- PIA GÜNTHER, MANUELA GUSKY, LARS GUTOW, WILFRIED HEIBER, PETRA JANTSCHIK, HANS- JOACHIM KRIEG,ROLAND KRONE, PETRA NEHMER,KATHARINA REICHERT, HENNING REISS, ALEXANDER SCHRÖDER, JAN WITT und MICHAEL LOTHAR ZETTLER unter Mitarbeit von MAREIKE GÜTH Zusammenfassung Inden hier vorgelegten Listen für amMeeresbodenlebende wirbellose Tiere (Makrozoo- benthos) aus neun Tierstämmen wurden 1.244 Arten bewertet. Eszeigt sich, dass die Verhältnis- se in den deutschen Meeresgebietender Nord-und Ostsee (inkl.
    [Show full text]
  • The Limpet Form in Gastropods: Evolution, Distribution, and Implications for the Comparative Study of History
    UC Davis UC Davis Previously Published Works Title The limpet form in gastropods: Evolution, distribution, and implications for the comparative study of history Permalink https://escholarship.org/uc/item/8p93f8z8 Journal Biological Journal of the Linnean Society, 120(1) ISSN 0024-4066 Author Vermeij, GJ Publication Date 2017 DOI 10.1111/bij.12883 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Biological Journal of the Linnean Society, 2016, , – . With 1 figure. Biological Journal of the Linnean Society, 2017, 120 , 22–37. With 1 figures 2 G. J. VERMEIJ A B The limpet form in gastropods: evolution, distribution, and implications for the comparative study of history GEERAT J. VERMEIJ* Department of Earth and Planetary Science, University of California, Davis, Davis, CA,USA C D Received 19 April 2015; revised 30 June 2016; accepted for publication 30 June 2016 The limpet form – a cap-shaped or slipper-shaped univalved shell – convergently evolved in many gastropod lineages, but questions remain about when, how often, and under which circumstances it originated. Except for some predation-resistant limpets in shallow-water marine environments, limpets are not well adapted to intense competition and predation, leading to the prediction that they originated in refugial habitats where exposure to predators and competitors is low. A survey of fossil and living limpets indicates that the limpet form evolved independently in at least 54 lineages, with particularly frequent origins in early-diverging gastropod clades, as well as in Neritimorpha and Heterobranchia. There are at least 14 origins in freshwater and 10 in the deep sea, E F with known times ranging from the Cambrian to the Neogene.
    [Show full text]
  • Marine Ecology Progress Series 555:79
    The following supplements accompany the article Spatial and temporal structure of the meroplankton community in a sub- Arctic shelf system Marc J. Silberberger*, Paul E. Renaud, Boris Espinasse, Henning Reiss *Corresponding author: [email protected] Marine Ecology Progress Series 555: 79–93 (2016) SUPPLEMENTS Supplement 1. Compiled list of sampled taxa Crustacea: Decapoda: Galathea sp. Munida sp. Philocheras bispinosus bispinosus Carcinus maenas Cancer pagurus Caridion gordoni Eualus pusiolus Lebbeus sp. Polybiidae Hyas sp. Pandalus montagui Atlantopandalus propinqvus Pagurus bernhardus Pagurus pubescens Anapagurus sp. Anapagurus laevis Cirripedia: Verruca stroemia Balanus balanus Semibalanus balanoides Balanus crenatus Lepadidae Bryozoa: Membranipora membranacea Electra pilosa Polychaeta: Amphinomidae Chaetopteridae Spionidae Phyllodocidae 1 Pectinariidae Nephtyidae Polynoidae Aphroditidae Arenicolidae Trochophora (unknown) Syllidae Mollusca: Bivalvia: Hiatella – Type Mya – Type Mytilidae – Type Cardiidae – Type Anomiidae – Type Gastropoda: Velutina velutina Lamellaria latens Lamellaria perspicua Trivia arctica Littorinimorpha – Type Raphitoma linearis Mangelia attenuata Turritella communis Melanella sp. Nudibranchia Pleurobranchomorpha Cephalaspidea & Sacoglossa Pyramidellidae Echinodermata: Ophiuroidea Echinoidea Asteroidea Holothuroidea Various: Nemertea Enteropneusta Phoronida Sipuncula Platyhelminthes Hydrozoa (Actinula) Anthozoa Planula Ascidiacea Unidentified
    [Show full text]
  • 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.
    [Show full text]
  • Marine Ecology Progress Series 228:153
    MARINE ECOLOGY PROGRESS SERIES Vol. 228: 153–163, 2002 Published March 6 Mar Ecol Prog Ser Carnivore/non-carnivore ratios in northeastern Pacific marine gastropods James W. Valentine1,*, Kaustuv Roy2, David Jablonski3 1Department of Integrative Biology and Museum of Paleontology, University of California, Berkeley, California 94720, USA 2Ecology, Behavior and Evolution Section, Division of Biology, University of California at San Diego, 9500 Gilman Drive, La Jolla, California 92093-0116, USA 3Department of Geophysical Sciences, University of Chicago, 5734 Ellis Avenue, Chicago, Illinois 60637, USA ABSTRACT: For 2321 species of shelled gastropods of the northeastern Pacific, the ratio of carnivo- rous to non-carnivorous species (C/NC ratio), computed for each degree of latitude, reveals striking spatial changes, with tropical and arctic areas characterized by high values and with the mid- latitudes having the lowest ratios. This latitudinal trend is markedly different from trends for terres- trial clades. The zonal variation in C/NC ratios within bins is largely due to differences in geographic ranges of the groups; for example, tropical carnivorous species range farther than non-carnivorous ones, thus overlapping them in more latitudinal bins. Differences in the distribution and diversity of carnivorous and non-carnivorous species may arise from a number of sources, including variability of primary production in the tropical eastern Pacific, patchiness of substrates to which non-carnivores are adapted, narrow dietary specializations of tropical carnivores, and higher provinciality found in extratropical regions. KEY WORDS: Trophic ratios · Latitudinal diversity trends · Provinciality · Variable productivity Resale or republication not permitted without written consent of the publisher INTRODUCTION diversities (Faaborg 1985, Jeffries & Lawton 1985, Karr et al.
    [Show full text]
  • Velutina Schneideri (Friele, 1886, )
    Arctic Megabenthos Velutina schneideri (Friele, 1886, ) Phylum: Mollusca Class: Gastropoda Order: Littorinimorpha Family: Velutinidae Genus: Velutina Description. Shell broadly ear-shaped, with 2.5 convex rounded whorls and deeply impressed suture. Spire projects slightly above last whorl. Protoconch one-whorled, uncovered by periostracum. Last whorl moderately convex. Peri¬ostracum yellow or light brown, less developed than calcareous layer, occasion¬ally obsolete on spiral surface. Sculpture of frequently disposed growth lines crossing spiral ribs. The latter not only present on periostracum but also on calcareous layer. Riblets vary greatly in number and frequency. Last whorl usually with 12-22 riblets with intervals near shell edge exceeding their width by 2-4 times. Aperture roundly oval, with thickened edge because of periostracum. Calcareous lining of aperture bluish-white, opaque. Measurements. Largest seen specimen: height 8.8 mm, length 15.5 mm, width 13.5 mm. Remarks. - Because of great variability most investigators consider this species synonymous with V. (V.) velutina. In typical V.(V.) schneideri, riblets are delicate and disposed at intervals 4-5 times their width and not exceeding 20 in number; occasionally they are not well developed. Specimens morphologically similar to V.(V.) velutina have wider riblets, and intervals exceed the width 2-3 times. Periostracum usually is better developed. The shape of penis easily distinguish the species. In V.(V.) schneideri it is wide and flattened at the base, terminating into a pointed long flagellated appendage. In V.(V.) velutina, penis is in form of a broad cylinder bordered by wide folds at the end. Distribution. Greenland, the Norwegian, Barents, Kara, Laptev and East Siber¬ian Seas as well as North Kurile Strait.
    [Show full text]
  • Caenogastropoda
    13 Caenogastropoda Winston F. Ponder, Donald J. Colgan, John M. Healy, Alexander Nützel, Luiz R. L. Simone, and Ellen E. Strong Caenogastropods comprise about 60% of living Many caenogastropods are well-known gastropod species and include a large number marine snails and include the Littorinidae (peri- of ecologically and commercially important winkles), Cypraeidae (cowries), Cerithiidae (creep- marine families. They have undergone an ers), Calyptraeidae (slipper limpets), Tonnidae extraordinary adaptive radiation, resulting in (tuns), Cassidae (helmet shells), Ranellidae (tri- considerable morphological, ecological, physi- tons), Strombidae (strombs), Naticidae (moon ological, and behavioral diversity. There is a snails), Muricidae (rock shells, oyster drills, etc.), wide array of often convergent shell morpholo- Volutidae (balers, etc.), Mitridae (miters), Buccin- gies (Figure 13.1), with the typically coiled shell idae (whelks), Terebridae (augers), and Conidae being tall-spired to globose or fl attened, with (cones). There are also well-known freshwater some uncoiled or limpet-like and others with families such as the Viviparidae, Thiaridae, and the shells reduced or, rarely, lost. There are Hydrobiidae and a few terrestrial groups, nota- also considerable modifi cations to the head- bly the Cyclophoroidea. foot and mantle through the group (Figure 13.2) Although there are no reliable estimates and major dietary specializations. It is our aim of named species, living caenogastropods are in this chapter to review the phylogeny of this one of the most diverse metazoan clades. Most group, with emphasis on the areas of expertise families are marine, and many (e.g., Strombidae, of the authors. Cypraeidae, Ovulidae, Cerithiopsidae, Triphori- The fi rst records of undisputed caenogastro- dae, Olividae, Mitridae, Costellariidae, Tereb- pods are from the middle and upper Paleozoic, ridae, Turridae, Conidae) have large numbers and there were signifi cant radiations during the of tropical taxa.
    [Show full text]
  • Energy Values of Marine Benthic Invertebrates from the Canadian Arctic
    MARINE ECOLOGY - PROGRESS SERIES Published September 10 Mar. Ecol. Prog. Ser. 1 Energy values of marine benthic invertebrates from the Canadian Arctic J. W. Wacasey, E. G.Atkinson Arctic Biological Station, Department of Fisheries and Oceans, 555 St. Pierre Boulevard, Ste-Anne-de-Bellevue, Quebec H9X 3R4,Canada ABSTRACT: Calonc values were determined for 121 species of cold-water benthic invertebrates, 109 of which are representative of a soft bottom community in Frobisher Bay, Northwest Territories (Canada). The mean calonc value for the community was 5.424 kcal g-' ash-free dry weight (SD f 0.403). This is not significantly different from values from lower latitudes, as has been suggested for planktonic communities. With one exception, the Ascidiacea, there were no significant differences in mean caloric value among major taxa. The lnterspecific distnbution of AFDW caloric value is discussed; present data support the growlng evidence that the natural pattern is symmetrical with values concentrated about a mean of 5.4 to 5.7 kcal g-' AFDW for benthic invertebrates. Caloric equivalents for biomass estimates and large-scale community comparisons may be derived from the regression of dry weight caloric value on percent organic content (dry weight): Y (kcal g-' AFDW) = -0.3897 + 0.0605 X (% organic content). when the organic fraction is determined directly. Two problematical taxa, Porifera and Echinodermata, are discussed and separate regressions are presented. INTRODUCTION community mean value, taxonomic variations, and interspecific distribution pattern of caloric values is Although energy values of many cold-water marine discussed. The relationships between caloric value and zoobenthic invertebrates are available (Ellis 1960, organic content gives equations from which fast, reli- Brawn et al.
    [Show full text]
  • Coastal Marine Institute Epibenthic Community Variability on The
    University of Alaska Coastal Marine Institute Epibenthic Community Variability on the Alaskan Beaufort Sea Continental Shelf Principal Investigator: Brenda Konar, University of Alaska Fairbanks Collaborator: Alexandra M. Ravelo, University of Alaska Fairbanks Final Report May 201 3 OCS Study BOEM 2013-01148 Contact Information: email: [email protected] phone: 907.474.6782 fax: 907.474.7204 Coastal Marine Institute School of Fisheries and Ocean Sciences University of Alaska Fairbanks P. O. Box 757220 Fairbanks, AK 99775-7220 This study was funded in part by the U.S. Department of the Interior, Bureau of Ocean Energy Management (BOEM) through Cooperative Agreement M11AC00002 between BOEM, Alaska Outer Continental Shelf Region, and the University of Alaska Fairbanks. This report, OCS Study BOEM 2013-01148, is available through the Coastal Marine Institute, select federal depository libraries and http://www.boem.gov/Environmental-Stewardship/Environmental-Studies/Alaska-Region/Index.aspx. The views and conclusions contained in this document are those of the authors and should not be interpreted as representing the opinions or policies of the U.S. Government. Mention of trade names or commercial products does not constitute their endorsement by the U.S. Government. Contents Figures ............................................................................................................................................. iii Tables .............................................................................................................................................
    [Show full text]
  • Spermatogenesis of the Gastropod, Pila Globosa, with S Pecial
    1959 423 Spermatogenesis of the Gastropod , Pila globosa, with S pecial Reference to the Cytoplasmic Organelles G. P. Sharma, Brij L. Gupta , and O. P. Mittal Department of Zoology, Panjab University , Hoshiarpur, Punjab, India Received December 22, 1958 Introduction The gastropods constitute the classical material for the study of sperma togenesis. The two most important aspects which have been the subject of controversy for the cytologists are the acrosome formation and the dimorphic sperms. Whereas the disagreement regarding the acrosome formation has been in the pulmonates, the problem of dimorphic sperms is restricted to the order prosobranchia of the class Gastropoda. According to Wilson (1925), von Siebold (1837) was the first worker to report dispermy in the prosobranch, Paludina (now called Viviparus). He described two types of sperms, viz., worm-shaped or oligopyrene, and the hair-shaped or eupyrene. This preliminary report of von Siebold was later on confirmed and ex tended by a number of subsequent workers like Meves (1902), Gatenby (1919), Ankel (1924), Alexenko (1926), Tuzet (1930), Woodard (1940), Pol lister and Pollister (1943) etc., in Viviparus (Paludina) vivipara, and a number of other prosobranchs. All of these workers have based their obser vations on the fixed and sectioned material. Pollister and Pollister (1943) have, however, studied only the chromosomes and centrosomes in both the eupyrene and the oligopyrene sperms of Viviparus vivipara. Recently Hanson et al. (1952) have worked out the detailed structure of the eupyrene and the oligopyrene sperms in the prosobranch, Viviparus. These authors examined the living cells under the phase-contrast microscope and the fixed material with the electron microscope and the various cyto chemical techniques.
    [Show full text]