Identity of Turbo Bryereus Montagu, Description of a New Rissoidae
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Regional Studies in Marine Science Artificial Substrates As Sampling
Regional Studies in Marine Science 37 (2020) 101331 Contents lists available at ScienceDirect Regional Studies in Marine Science journal homepage: www.elsevier.com/locate/rsma Artificial substrates as sampling devices for marine epibenthic fauna: A quest for standardization ∗ Diego Carreira-Flores a,b,c, , Regina Neto a, Hugo Ferreira a, Edna Cabecinha c, Guillermo Díaz-Agras b, Pedro T. Gomes a a Centre of Molecular and Environmental Biology, Department of Biology, University of Minho, Portugal b Marine Biology Station of A Graña, University of Santiago de Compostela, Spain c Centre for the Research and Technology of Agro-Environmental and Biological Sciences (CITAB), Department of Biology and Environment, University of Trás-os montes and Alto Douro, Portugal article info a b s t r a c t Article history: In temperate regions, macroalgae are naturally abundant habitat builders for many organisms of Received 6 March 2020 ecological and economic importance. Hence, macroalgae are good targets for monitoring studies based Received in revised form 12 May 2020 on colonization processes as, through them, it is possible to sample the epifauna that uses them as Accepted 28 May 2020 habitat. Nevertheless, macroalgae collection may not be sustainable, can compromise the survival of Available online 30 May 2020 the target macroalgae populations and destroy fragile or threatened communities. Keywords: The search for an adequate procedure that can overcome the problems related to destructive Epifaunal assemblages quantitative sampling of the epifauna associated with macroalgae and the development of a method- Macroalgae ology that can be used for comparative macrofauna monitoring, regardless of the location, were the Artificial Seaweed Monitoring Structures motivations for this study. -
SNH Commissioned Report 765: Seagrass (Zostera) Beds in Orkney
Scottish Natural Heritage Commissioned Report No. 765 Seagrass (Zostera) beds in Orkney COMMISSIONED REPORT Commissioned Report No. 765 Seagrass (Zostera) beds in Orkney For further information on this report please contact: Kate Thompson Scottish Natural Heritage 54-56 Junction Road KIRKWALL Orkney KW15 1AW Telephone: 01856 875302 E-mail: [email protected] This report should be quoted as: Thomson, M. and Jackson, E, with Kakkonen, J. 2014. Seagrass (Zostera) beds in Orkney. Scottish Natural Heritage Commissioned Report No. 765. This report, or any part of it, should not be reproduced without the permission of Scottish Natural Heritage. This permission will not be withheld unreasonably. The views expressed by the author(s) of this report should not be taken as the views and policies of Scottish Natural Heritage. © Scottish Natural Heritage 2014. COMMISSIONED REPORT Summary Seagrass (Zostera) beds in Orkney Commissioned Report No. 765 Project No: 848 Contractors: Emma Jackson (The Marine Biological Association of the United Kingdom) and Malcolm Thomson (Sula Diving) Year of publication: 2014 Keywords Seagrass; Zostera marina; Orkney; predictive model; survey. Background Seagrasses (Zostera spp) are marine flowering plants that develop on sands and muds in sheltered intertidal and shallow subtidal areas. Seagrass beds are important marine habitats but are vulnerable to a range of human induced pressures. Their vulnerability and importance to habitat creation and ecological functioning is recognised in their inclusion on the recommended Priority Marine Features list for Scotland’s seas. Prior to this study, there were few confirmed records of Zostera in Orkney waters. This study combined a predictive modelling approach with boat-based surveys to enhance under- standing of seagrass distribution in Orkney and inform conservation management. -
Laboratory Reference Module Summary Report LR22
Laboratory Reference Module Summary Report Benthic Invertebrate Component - 2017/18 LR22 26 March 2018 Author: Tim Worsfold Reviewer: David Hall, NMBAQCS Project Manager Approved by: Myles O'Reilly, Contract Manager, SEPA Contact: [email protected] MODULE / EXERCISE DETAILS Module: Laboratory Reference (LR) Exercises: LR22 Data/Sample Request Circulated: 10th July 2017 Sample Submission Deadline: 31st August 2017 Number of Subscribing Laboratories: 7 Number of LR Received: 4 Contents Table 1. Summary of mis-identified taxa in the Laboratory Reference module (LR22) (erroneous identifications in brackets). Table 2. Summary of identification policy differences in the Laboratory Reference Module (LR22) (original identifications in brackets). Appendix. LR22 individual summary reports for participating laboratories. Table 1. Summary of mis-identified taxa in the Laboratory Reference Module (LR22) (erroneous identifications in brackets). Taxonomic Major Taxonomic Group LabCode Edits Polychaeta Oligochaeta Crustacea Mollusca Other Spio symphyta (Spio filicornis ) - Leucothoe procera (Leucothoe ?richardii ) - - Scolelepis bonnieri (Scolelepis squamata ) - - - - BI_2402 5 Laonice (Laonice sarsi ) - - - - Dipolydora (Dipolydora flava ) - - - - Goniada emerita (Goniadella bobrezkii ) - Nebalia reboredae (Nebalia bipes ) - - Polydora sp. A (Polydora cornuta ) - Diastylis rathkei (Diastylis cornuta ) - - BI_2403 7 Syllides? (Anoplosyllis edentula ) - Abludomelita obtusata (Tryphosa nana ) - in mixture - - Spirorbinae (Ditrupa arietina ) - - - - -
WMSDB - Worldwide Mollusc Species Data Base
WMSDB - Worldwide Mollusc Species Data Base Family: TURBINIDAE Author: Claudio Galli - [email protected] (updated 07/set/2015) Class: GASTROPODA --- Clade: VETIGASTROPODA-TROCHOIDEA ------ Family: TURBINIDAE Rafinesque, 1815 (Sea) - Alphabetic order - when first name is in bold the species has images Taxa=681, Genus=26, Subgenus=17, Species=203, Subspecies=23, Synonyms=411, Images=168 abyssorum , Bolma henica abyssorum M.M. Schepman, 1908 aculeata , Guildfordia aculeata S. Kosuge, 1979 aculeatus , Turbo aculeatus T. Allan, 1818 - syn of: Epitonium muricatum (A. Risso, 1826) acutangulus, Turbo acutangulus C. Linnaeus, 1758 acutus , Turbo acutus E. Donovan, 1804 - syn of: Turbonilla acuta (E. Donovan, 1804) aegyptius , Turbo aegyptius J.F. Gmelin, 1791 - syn of: Rubritrochus declivis (P. Forsskål in C. Niebuhr, 1775) aereus , Turbo aereus J. Adams, 1797 - syn of: Rissoa parva (E.M. Da Costa, 1778) aethiops , Turbo aethiops J.F. Gmelin, 1791 - syn of: Diloma aethiops (J.F. Gmelin, 1791) agonistes , Turbo agonistes W.H. Dall & W.H. Ochsner, 1928 - syn of: Turbo scitulus (W.H. Dall, 1919) albidus , Turbo albidus F. Kanmacher, 1798 - syn of: Graphis albida (F. Kanmacher, 1798) albocinctus , Turbo albocinctus J.H.F. Link, 1807 - syn of: Littorina saxatilis (A.G. Olivi, 1792) albofasciatus , Turbo albofasciatus L. Bozzetti, 1994 albofasciatus , Marmarostoma albofasciatus L. Bozzetti, 1994 - syn of: Turbo albofasciatus L. Bozzetti, 1994 albulus , Turbo albulus O. Fabricius, 1780 - syn of: Menestho albula (O. Fabricius, 1780) albus , Turbo albus J. Adams, 1797 - syn of: Rissoa parva (E.M. Da Costa, 1778) albus, Turbo albus T. Pennant, 1777 amabilis , Turbo amabilis H. Ozaki, 1954 - syn of: Bolma guttata (A. Adams, 1863) americanum , Lithopoma americanum (J.F. -
Phylum MOLLUSCA
285 MOLLUSCA: SOLENOGASTRES-POLYPLACOPHORA Phylum MOLLUSCA Class SOLENOGASTRES Family Lepidomeniidae NEMATOMENIA BANYULENSIS (Pruvot, 1891, p. 715, as Dondersia) Occasionally on Lafoea dumosa (R.A.T., S.P., E.J.A.): at 4 positions S.W. of Eddystone, 42-49 fm., on Lafoea dumosa (Crawshay, 1912, p. 368): Eddystone, 29 fm., 1920 (R.W.): 7, 3, 1 and 1 in 4 hauls N.E. of Eddystone, 1948 (V.F.) Breeding: gonads ripe in Aug. (R.A.T.) Family Neomeniidae NEOMENIA CARINATA Tullberg, 1875, p. 1 One specimen Rame-Eddystone Grounds, 29.12.49 (V.F.) Family Proneomeniidae PRONEOMENIA AGLAOPHENIAE Kovalevsky and Marion [Pruvot, 1891, p. 720] Common on Thecocarpus myriophyllum, generally coiled around the base of the stem of the hydroid (S.P., E.J.A.): at 4 positions S.W. of Eddystone, 43-49 fm. (Crawshay, 1912, p. 367): S. of Rame Head, 27 fm., 1920 (R.W.): N. of Eddystone, 29.3.33 (A.J.S.) Class POLYPLACOPHORA (=LORICATA) Family Lepidopleuridae LEPIDOPLEURUS ASELLUS (Gmelin) [Forbes and Hanley, 1849, II, p. 407, as Chiton; Matthews, 1953, p. 246] Abundant, 15-30 fm., especially on muddy gravel (S.P.): at 9 positions S.W. of Eddystone, 40-43 fm. (Crawshay, 1912, p. 368, as Craspedochilus onyx) SALCOMBE. Common in dredge material (Allen and Todd, 1900, p. 210) LEPIDOPLEURUS, CANCELLATUS (Sowerby) [Forbes and Hanley, 1849, II, p. 410, as Chiton; Matthews. 1953, p. 246] Wembury West Reef, three specimens at E.L.W.S.T. by J. Brady, 28.3.56 (G.M.S.) Family Lepidochitonidae TONICELLA RUBRA (L.) [Forbes and Hanley, 1849, II, p. -
Early Ontogeny and Palaeoecology of the Mid−Miocene Rissoid Gastropods of the Central Paratethys
Early ontogeny and palaeoecology of the Mid−Miocene rissoid gastropods of the Central Paratethys THORSTEN KOWALKE and MATHIAS HARZHAUSER Kowalke, T. and Harzhauser, M. 2004. Early ontogeny and palaeoecology of the Mid−Miocene rissoid gastropods of the Central Paratethys. Acta Palaeontologica Polonica 49 (1): 111–134. Twenty−six species of Rissoidae (Caenogastropoda: Littorinimorpha: Rissooidea) are described from the Badenian and Early Sarmatian of 14 localities in Austria and the Czech Republic (Molasse Basin, Styrian Basin, Vienna Basin) and from the Badenian of Coştei (Romania). For the first time, the early ontogenetic skeletal characters of these gastropods are de− scribed. Based on these features an indirect larval development with a planktotrophic veliger could be reconstructed for all investigated Mid−Miocene species. The status of Mohrensterniinae as a subfamily of the Rissoidae is confirmed by the mor− phology of the low conical protoconch, consisting of a fine spirally sculptured embryonic shell and a larval shell which is smooth except for growth lines. Transitions from embryonic shells to larval shells and from larval shells to teleoconchs are slightly thickened and indistinct. Whilst representatives of the subfamily Rissoinae characterise the marine Badenian assem− blages, Mohrensterniinae predominate the Early Sarmatian faunas. We hypothesize that this take−over by the Mohren− sterniinae was triggered by changes in the water chemistry towards polyhaline conditions. Consequently, the shift towards hypersaline conditions in the Late Sarmatian is mirrored by the abrupt decline of the subfamily. Four new species Rissoa costeiensis (Rissoinae) from the Badenian and Mohrensternia hollabrunnensis, Mohrensternia pfaffstaettensis,and Mohrensternia waldhofensis (Mohrensterniinae) from the Early Sarmatian are introduced. -
Endemic Species of Christmas Island, Indian Ocean D.J
RECORDS OF THE WESTERN AUSTRALIAN MUSEUM 34 055–114 (2019) DOI: 10.18195/issn.0312-3162.34(2).2019.055-114 Endemic species of Christmas Island, Indian Ocean D.J. James1, P.T. Green2, W.F. Humphreys3,4 and J.C.Z. Woinarski5 1 73 Pozieres Ave, Milperra, New South Wales 2214, Australia. 2 Department of Ecology, Environment and Evolution, La Trobe University, Melbourne, Victoria 3083, Australia. 3 Western Australian Museum, Locked Bag 49, Welshpool DC, Western Australia 6986, Australia. 4 School of Biological Sciences, The University of Western Australia, 35 Stirling Highway, Crawley, Western Australia 6009, Australia. 5 NESP Threatened Species Recovery Hub, Charles Darwin University, Casuarina, Northern Territory 0909, Australia, Corresponding author: [email protected] ABSTRACT – Many oceanic islands have high levels of endemism, but also high rates of extinction, such that island species constitute a markedly disproportionate share of the world’s extinctions. One important foundation for the conservation of biodiversity on islands is an inventory of endemic species. In the absence of a comprehensive inventory, conservation effort often defaults to a focus on the better-known and more conspicuous species (typically mammals and birds). Although this component of island biota often needs such conservation attention, such focus may mean that less conspicuous endemic species (especially invertebrates) are neglected and suffer high rates of loss. In this paper, we review the available literature and online resources to compile a list of endemic species that is as comprehensive as possible for the 137 km2 oceanic Christmas Island, an Australian territory in the north-eastern Indian Ocean. -
Gastropoda: Rissoidae) in the Lower Miocene of Valle Ceppi (Torino, NW Italy
Bollettino della Società Paleontologica Italiana, 48 (1), 2009, 51-57. Modena, 15 maggio 200951 Two new species of Rissoina (Gastropoda: Rissoidae) in the Lower Miocene of Valle Ceppi (Torino, NW Italy) Marta ZUNINO & Giulio PAVIA M. Zunino, Dipartimento di Scienze della Terra, Università degli Studi di Torino, Via Valperga Caluso 35, I-10125 Torino, Italy; [email protected] G. Pavia, Dipartimento di Scienze della Terra, Università degli Studi di Torino, Via Valperga Caluso 35, I-10125 Torino, Italy; [email protected] KEY WORDS - Rissoidae, Rissoina, Lower Miocene, Valle Ceppi, Torino Hills, Tertiary Piedmont Basin. ABSTRACT - Two new species of Rissoina from the Miocene of Torino Hills, Rissoina (R.) giuntellii and Rissoina (R.) sturanii, are described in this paper. Rissoina (R.) giuntellii n. sp. is frequent in the Lower Miocene deposits of Valle Ceppi and in coeval and more recent layers of Torino Hills; it is characterized by a small shell with convex whorls, the sculpture is composed by prominent axial ribs and cords visible at the base of the last whorl. Rissoina (R.) sturanii n. sp. is only known from the Valle Ceppi section; it is characterized by medium-sized shells with flat whorls and very fine axial and spiral ornamentation. Because of the reduced number of specimens and their state of conservation, scanning electron microscope photographs were used to study shell micro-architecture where possible. Comparison with the coeval Rissoininae known from the deposits of Paratethys, Aquitaine Basin and Loire Basin confirmed the election of Rissoina (R.) giuntellii n. sp. and Rissoina (R.) sturanii n. sp., currently known only in the Miocene deposits of the Tertiary Piedmont Basin. -
Worms - World Register of Marine Species 15/01/12 08:52
WoRMS - World Register of Marine Species 15/01/12 08:52 http://www.marinespecies.org/aphia.php?p=taxlist WoRMS Taxon list http://www.marinespecies.org/aphia.php?p=taxlist 405 matching records, showing records 1-100. Rissoa Freminville in Desmarest, 1814 Rissoa aartseni Verduin, 1985 Rissoa aberrans C. B. Adams, 1850 accepted as Stosicia aberrans (C. B. Adams, 1850) Rissoa albella Lovén, 1846 accepted as Pusillina sarsii (Lovén, 1846) Rissoa albella Alder, 1844 accepted as Rissoella diaphana (Alder, 1848) Rissoa albella rufilabrum Alder accepted as Rissoa lilacina Récluz, 1843 Rissoa albugo Watson, 1873 Rissoa alifera Thiele, 1925 accepted as Hoplopteron alifera (Thiele, 1925) Rissoa alleryi (Nordsieck, 1972) Rissoa angustior (Monterosato, 1917) Rissoa atomus E. A. Smith, 1890 Rissoa auriformis Pallary, 1904 Rissoa auriscalpium (Linnaeus, 1758) Rissoa basispiralis Grant-Mackie & Chapman-Smith, 1971 † accepted as Diala semistriata (Philippi, 1849) Rissoa boscii (Payraudeau, 1826) accepted as Melanella polita (Linnaeus, 1758) Rissoa calathus Forbes & Hanley, 1850 accepted as Alvania beanii (Hanley in Thorpe, 1844) Rissoa cerithinum Philippi, 1849 accepted as Cerithidium cerithinum (Philippi, 1849) Rissoa coriacea Manzoni, 1868 accepted as Talassia coriacea (Manzoni, 1868) Rissoa coronata Scacchi, 1844 accepted as Opalia hellenica (Forbes, 1844) Rissoa costata (J. Adams, 1796) accepted as Manzonia crassa (Kanmacher, 1798) Rissoa costulata Alder, 1844 accepted as Rissoa guerinii Récluz, 1843 Rissoa crassicostata C. B. Adams, 1845 accepted as Opalia hotessieriana (d’Orbigny, 1842) Rissoa cruzi Castellanos & Fernández, 1974 accepted as Alvania cruzi (Castellanos & Fernández, 1974) Rissoa cumingii Reeve, 1849 accepted as Rissoina striata (Quoy & Gaimard, 1833) Rissoa curta Dall, 1927 Rissoa decorata Philippi, 1846 Rissoa deformis G.B. -
Phylogenetic Relationships of the Cochliopinae (Rissooidea: Hydrobiidae): an Enigmatic Group of Aquatic Gastropods Hsiu-Ping Liu,* Robert Hershler,†,1 and Fred G
Molecular Phylogenetics and Evolution Vol. 21, No. 1, October, pp. 17–25, 2001 doi:10.1006/mpev.2001.0988, available online at http://www.idealibrary.com on Phylogenetic Relationships of the Cochliopinae (Rissooidea: Hydrobiidae): An Enigmatic Group of Aquatic Gastropods Hsiu-Ping Liu,* Robert Hershler,†,1 and Fred G. Thompson‡ *Department of Biology, Southwest Missouri State University, 901 South National Avenue, Springfield, Missouri 65804-0095; †Department of Systematic Biology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560-0118; and ‡Florida Museum of Natural History, University of Florida, Gainesville, Florida 32611-7800 Received July 24, 2000; revised March 27, 2001 shler, 1993) have not been well tested as there is no Phylogenetic analysis based on a partial sequence of rigorously proposed analysis of relationships that in- the mitochondrial cytochrome c oxidase subunit I cludes more than a trivial sampling of this large group gene was performed for 26 representatives of the (e.g., Altaba, 1993; Ponder et al., 1993; Ponder, 1999). aquatic gastropod subfamily Cochliopinae, 6 addi- Phylogenetic reconstructions of these animals have tional members of the family Hydrobiidae, and out- been hampered by a paucity of apparent synapomor- group species of the families Rissoidae and Pomatiop- phies (Thompson, 1984), putatively extensive ho- sidae. Maximum-parsimony analysis yielded a single moplasy (Davis, 1988; Hershler and Thompson, 1992), shortest tree which resolved two monophyletic and difficulties in reconciling homology (Hershler and groups: (1) a clade containing all cochliopine taxa with Ponder, 1998). Whereas a recent survey and reassess- the exception of Antroselates and (2) a clade composed of Antroselates and the hydrobiid genus Amnicola. -
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. -
Florida Keys Species List
FKNMS Species List A B C D E F G H I J K L M N O P Q R S T 1 Marine and Terrestrial Species of the Florida Keys 2 Phylum Subphylum Class Subclass Order Suborder Infraorder Superfamily Family Scientific Name Common Name Notes 3 1 Porifera (Sponges) Demospongia Dictyoceratida Spongiidae Euryspongia rosea species from G.P. Schmahl, BNP survey 4 2 Fasciospongia cerebriformis species from G.P. Schmahl, BNP survey 5 3 Hippospongia gossypina Velvet sponge 6 4 Hippospongia lachne Sheepswool sponge 7 5 Oligoceras violacea Tortugas survey, Wheaton list 8 6 Spongia barbara Yellow sponge 9 7 Spongia graminea Glove sponge 10 8 Spongia obscura Grass sponge 11 9 Spongia sterea Wire sponge 12 10 Irciniidae Ircinia campana Vase sponge 13 11 Ircinia felix Stinker sponge 14 12 Ircinia cf. Ramosa species from G.P. Schmahl, BNP survey 15 13 Ircinia strobilina Black-ball sponge 16 14 Smenospongia aurea species from G.P. Schmahl, BNP survey, Tortugas survey, Wheaton list 17 15 Thorecta horridus recorded from Keys by Wiedenmayer 18 16 Dendroceratida Dysideidae Dysidea etheria species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 19 17 Dysidea fragilis species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 20 18 Dysidea janiae species from G.P. Schmahl, BNP survey; Tortugas survey, Wheaton list 21 19 Dysidea variabilis species from G.P. Schmahl, BNP survey 22 20 Verongida Druinellidae Pseudoceratina crassa Branching tube sponge 23 21 Aplysinidae Aplysina archeri species from G.P. Schmahl, BNP survey 24 22 Aplysina cauliformis Row pore rope sponge 25 23 Aplysina fistularis Yellow tube sponge 26 24 Aplysina lacunosa 27 25 Verongula rigida Pitted sponge 28 26 Darwinellidae Aplysilla sulfurea species from G.P.