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Atlanta Ariejansseni, a New Species of Shelled Heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea)
A peer-reviewed open-access journal ZooKeys 604: 13–30 (2016) Atlanta ariejansseni, a new species of shelled heteropod.... 13 doi: 10.3897/zookeys.604.8976 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Atlanta ariejansseni, a new species of shelled heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea) Deborah Wall-Palmer1,2, Alice K. Burridge2,3, Katja T.C.A. Peijnenburg2,3 1 School of Geography, Earth and Environmental Sciences, Plymouth University, Drake Circus, Plymouth, PL4 8AA, UK 2 Naturalis Biodiversity Center, Darwinweg 2, 2333 CR Leiden, The Netherlands3 Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, P. O. Box 94248, 1090 GE Amster- dam, The Netherlands Corresponding author: Deborah Wall-Palmer ([email protected]) Academic editor: N. Yonow | Received 21 April 2016 | Accepted 22 June 2016 | Published 11 July 2016 http://zoobank.org/09E534C5-589D-409E-836B-CF64A069939D Citation: Wall-Palmer D, Burridge AK, Peijnenburg KTCA (2016) Atlanta ariejansseni, a new species of shelled heteropod from the Southern Subtropical Convergence Zone (Gastropoda, Pterotracheoidea). ZooKeys 604: 13–30. doi: 10.3897/zookeys.604.8976 Abstract The Atlantidae (shelled heteropods) is a family of microscopic aragonite shelled holoplanktonic gastro- pods with a wide biogeographical distribution in tropical, sub-tropical and temperate waters. The arago- nite shell and surface ocean habitat of the atlantids makes them particularly susceptible to ocean acidifica- tion and ocean warming, and atlantids are likely to be useful indicators of these changes. However, we still lack fundamental information on their taxonomy and biogeography, which is essential for monitoring the effects of a changing ocean. -
Abstract Volume
ABSTRACT VOLUME August 11-16, 2019 1 2 Table of Contents Pages Acknowledgements……………………………………………………………………………………………...1 Abstracts Symposia and Contributed talks……………………….……………………………………………3-225 Poster Presentations…………………………………………………………………………………226-291 3 Venom Evolution of West African Cone Snails (Gastropoda: Conidae) Samuel Abalde*1, Manuel J. Tenorio2, Carlos M. L. Afonso3, and Rafael Zardoya1 1Museo Nacional de Ciencias Naturales (MNCN-CSIC), Departamento de Biodiversidad y Biologia Evolutiva 2Universidad de Cadiz, Departamento CMIM y Química Inorgánica – Instituto de Biomoléculas (INBIO) 3Universidade do Algarve, Centre of Marine Sciences (CCMAR) Cone snails form one of the most diverse families of marine animals, including more than 900 species classified into almost ninety different (sub)genera. Conids are well known for being active predators on worms, fishes, and even other snails. Cones are venomous gastropods, meaning that they use a sophisticated cocktail of hundreds of toxins, named conotoxins, to subdue their prey. Although this venom has been studied for decades, most of the effort has been focused on Indo-Pacific species. Thus far, Atlantic species have received little attention despite recent radiations have led to a hotspot of diversity in West Africa, with high levels of endemic species. In fact, the Atlantic Chelyconus ermineus is thought to represent an adaptation to piscivory independent from the Indo-Pacific species and is, therefore, key to understanding the basis of this diet specialization. We studied the transcriptomes of the venom gland of three individuals of C. ermineus. The venom repertoire of this species included more than 300 conotoxin precursors, which could be ascribed to 33 known and 22 new (unassigned) protein superfamilies, respectively. Most abundant superfamilies were T, W, O1, M, O2, and Z, accounting for 57% of all detected diversity. -
Midwater Data Sheet
MIDWATER TRAWL DATA SHEET RESEARCH VESSEL__________________________________(1/20/2013Version*) CLASS__________________;DATE_____________;NAME:_________________________; DEVICE DETAILS___________ LOCATION (OVERBOARD): LAT_______________________; LONG___________________________ LOCATION (AT DEPTH): LAT_______________________; LONG______________________________ LOCATION (START UP): LAT_______________________; LONG______________________________ LOCATION (ONBOARD): LAT_______________________; LONG______________________________ BOTTOM DEPTH_________; DEPTH OF SAMPLE:____________; DURATION OF TRAWL___________; TIME: IN_________AT DEPTH________START UP__________SURFACE_________ SHIP SPEED__________; WEATHER__________________; SEA STATE_________________; AIR TEMP______________ SURFACE TEMP__________; PHYS. OCE. NOTES______________________; NOTES_____________________________ INVERTEBRATES Lensia hostile_______________________ PHYLUM RADIOLARIA Lensia havock______________________ Family Tuscaroridae “Round yellow ones”___ Family Hippopodiidae Vogtia sp.___________________________ PHYLUM CTENOPHORA Family Prayidae Subfamily Nectopyramidinae Class Nuda "Pointed siphonophores"________________ Order Beroida Nectadamas sp._______________________ Family Beroidae Nectopyramis sp.______________________ Beroe abyssicola_____________________ Family Prayidae Beroe forskalii________________________ Subfamily Prayinae Beroe cucumis _______________________ Craseoa lathetica_____________________ Class Tentaculata Desmophyes annectens_________________ Subclass -
Biogeography and Genetic Diversity of the Atlantid Heteropods T ⁎ Deborah Wall-Palmera,B, , Alice K
Progress in Oceanography 160 (2018) 1–25 Contents lists available at ScienceDirect Progress in Oceanography journal homepage: www.elsevier.com/locate/pocean SCCWRP #1038 Biogeography and genetic diversity of the atlantid heteropods T ⁎ Deborah Wall-Palmera,b, , Alice K. Burridgeb,c, Erica Goetzed, Frank R. Stokvisb, Arie W. Janssenb, Lisette Mekkesb,c, María Moreno-Alcántarae, Nina Bednaršekf, Tom Schiøtteg, Martin Vinther Sørenseng, Christopher W. Smarta, Katja T.C.A. Peijnenburgb,c a School of Geography, Earth and Environmental Sciences, University of Plymouth, Plymouth PL4 8AA, UK b Naturalis Biodiversity Center, P.O. Box 9517, 2300 RA Leiden, The Netherlands c Institute for Biodiversity and Ecosystem Dynamics (IBED), University of Amsterdam, 1090 GE Amsterdam, The Netherlands d Department of Oceanography, University of Hawai‘iatMānoa, Honolulu, HI 96822, USA e Departamento de Plancton y Ecología Marina, Instituto Politécnico Nacional, Centro Interdisciplinario de Ciencias Marinas, La Paz C.P. 23096, Mexico f Southern California Coastal Waters Research Project, Harbor Blvd #110, Costa Mesa, CA 92626, USA g The Natural History Museum of Denmark, University of Copenhagen, 2100 Copenhagen, Denmark ARTICLE INFO ABSTRACT Keywords: The atlantid heteropods are regularly encountered, but rarely studied marine planktonic gastropods. Relying Atlantidae on a small (< 14 mm), delicate aragonite shell and living in the upper ocean means that, in common with Atlanta pteropods, atlantids are likely to be affected by imminent ocean changes. Variable shell morphology and Cytochrome c oxidase subunit 1 (mtCO1) widespread distributions indicate that the family is more diverse than the 23 currently known species. DNA barcoding Uncovering this diversity is fundamental to determining the distribution of atlantids and to understanding Planktonic gastropods their environmental tolerances. -
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. -
Toward a Global Reference Database of COI Barcodes for Marine Zooplankton
Marine Biology (2021) 168:78 https://doi.org/10.1007/s00227-021-03887-y REVIEW, CONCEPT, AND SYNTHESIS Toward a global reference database of COI barcodes for marine zooplankton Ann Bucklin1 · Katja T. C. A. Peijnenburg2,3 · Ksenia N. Kosobokova4 · Todd D. O’Brien5 · Leocadio Blanco‑Bercial6 · Astrid Cornils7 · Tone Falkenhaug8 · Russell R. Hopcroft9 · Aino Hosia10 · Silke Laakmann7,11 · Chaolun Li12 · Luis Martell10 · Jennifer M. Questel9 · Deborah Wall‑Palmer2 · Minxiao Wang12 · Peter H. Wiebe13 · Agata Weydmann‑Zwolicka14 Received: 6 February 2021 / Accepted: 18 April 2021 © The Author(s) 2021 Abstract Characterization of species diversity of zooplankton is key to understanding, assessing, and predicting the function and future of pelagic ecosystems throughout the global ocean. The marine zooplankton assemblage, including only metazoans, is highly diverse and taxonomically complex, with an estimated ~28,000 species of 41 major taxonomic groups. This review provides a comprehensive summary of DNA sequences for the barcode region of mitochondrial cytochrome oxidase I (COI) for identifed specimens. The foundation of this summary is the MetaZooGene Barcode Atlas and Database (MZGdb), a new open-access data and metadata portal that is linked to NCBI GenBank and BOLD data repositories. The MZGdb provides enhanced quality control and tools for assembling COI reference sequence databases that are specifc to selected taxonomic groups and/or ocean regions, with associated metadata (e.g., collection georeferencing, verifcation of species identifcation, molecular protocols), and tools for statistical analysis, mapping, and visualization. To date, over 150,000 COI sequences for ~ 5600 described species of marine metazoan plankton (including holo- and meroplankton) are available via the MZGdb portal. -
Primera Cita Para Aguas De Las Islas Canarias De Pterotrachea Scutata GEGENBAUR, 1855 (Mollusca: Gastropoda: Pterotracheoidea)
VIERAEA Vol. 36 81-89 Santa Cruz de Tenerife, octubre 2008 ISSN 0210-945X Primera cita para aguas de las islas Canarias de Pterotrachea scutata GEGENBAUR, 1855 (Mollusca: Gastropoda: Pterotracheoidea) ALEJANDRO DE VERA a,*, FERNANDO LOZANO SOLDEVILLA b, JOSÉ Mª. LANDEIRA b, Y FÁTIMA HERNÁNDEZ a a Departamento de Biología Marina, Museo de Ciencias Naturales, Cabildo de Tenerife, Apdo. Correos 853, E-38003 Santa Cruz de Tenerife, Canarias, España. b Departamento de Biología Animal (Ciencias Marinas), Facultad de Biología, Universidad de La Laguna. Avda. Astrofísico Francisco Sánchez s/n. 38206 La Laguna, Tenerife, Canarias, España. *[email protected] DE VERA, A., F. LOZANO SOLDEVILLA, J. Mª. LANDEIRA & F. HERNÁNDEZ (2008). First record from waters of Canary Islands of Pterotrachea scutata Gegenbaur, 1855 (Mollusca, Gastropoda, Pterotracheoidea). VIERAEA, 36: 81-89. RESUMEN: Se cita por primera vez para aguas de las islas Canarias a Pterotrachea scutata Gegenbaur, 1855 (Mollusca, Gastropoda, Pterotracheidae), recolectada al sureste de Fuerteventura, durante la realización de la campaña «FAX 9908». Se aportan las características morfológicas y morfométricas del ejemplar examinado, la distribución geográfica y batimétrica de la especie, así como una clave para la identificación de los miembros de la familia presentes en aguas de Canarias. Palabras clave: Mollusca, Pterotracheoidea, Pterotracheidae, Pterotrachea scutata, islas Canarias. ABSTRACT: Pterotrachea scutata Gegerbaur, 1855 (Mollusca, Gastropoda, Pterotracheidae) is recorded for the first time from waters of Canary Islands. The specimen was captured at the southeastern of Fuerteventura island during de «FAX 9908» cruise. Morphological and morphometric measurement of the specimen, geographic and bathymetric distribution of this species and a key to species of the family present in waters of the Canary Islands are given. -
Uva-DARE (Digital Academic Repository)
UvA-DARE (Digital Academic Repository) Evidence for the validity of Protatlanta sculpta (Gastropoda: Pterotracheoidea) Wall-Palmer, D.; Burridge, A.K.; Peijnenburg, K.T.C.A.; Janssen, A.; Goetze, E.; Kirby, R.; Hart, M.B.; Smart, C.W. Publication date 2016 Document Version Final published version Published in Contributions to Zoology License CC BY Link to publication Citation for published version (APA): Wall-Palmer, D., Burridge, A. K., Peijnenburg, K. T. C. A., Janssen, A., Goetze, E., Kirby, R., Hart, M. B., & Smart, C. W. (2016). Evidence for the validity of Protatlanta sculpta (Gastropoda: Pterotracheoidea). Contributions to Zoology, 85(4), 423-435. http://dpc.uba.uva.nl/cgi/t/text/text- idx?c=ctz;sid=389974472602fe97a330125123bf5da9;view=text;idno=m8504a03;rgn=div1;no de=m8504a03:1 General rights It is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), other than for strictly personal, individual use, unless the work is under an open content license (like Creative Commons). Disclaimer/Complaints regulations If you believe that digital publication of certain material infringes any of your rights or (privacy) interests, please let the Library know, stating your reasons. In case of a legitimate complaint, the Library will make the material inaccessible and/or remove it from the website. Please Ask the Library: https://uba.uva.nl/en/contact, or a letter to: Library of the University of Amsterdam, Secretariat, Singel 425, 1012 WP Amsterdam, The Netherlands. You will be contacted as soon as possible. UvA-DARE is a service provided by the library of the University of Amsterdam (https://dare.uva.nl) Download date:30 Sep 2021 Contributions to Zoology, 85 (4) 423-435 (2016) Evidence for the validity of Protatlanta sculpta (Gastropoda: Pterotracheoidea) Deborah Wall-Palmer1, 2, 6, Alice K. -
Heteropods (Gastropoda: Pterotracheoidea) Identified Along a Coastal-Oceanic Compound (+)-Discodermolide in the Caribbean Marine Sponge Discodermia Dissoluta
Boletín de Investigaciones Marinas y Costeras • Vol. 46 (2) • 2017 Sipkema, D., H.W. Blanch and R.H. Wijffels. 2006. Large-scale production of pharmaceuticals by marine sponges: sea, cells or synthesis? Abstracts, 7th Int. Instituto de Investigaciones Marinas y Costeras Boletin de Investigaciones Marinas y Costeras ISSN 0122-9761 Sponge Symp. Rio de Janeiro. 7-13 mayo 2006. “José Benito Vives de Andréis” Bulletin of Marine and Coastal Research Santa Marta, Colombia, 2017 Smith, A.B., B.S. Freeze, I. Brouard and T. Hirose. 2003. A practical improvement, enhancing the large-scale synthesis of (+)-discodermolide: A third- 46 (2), 175-181 generation approach. Org. Lett., 5: 4405-4408. Tziveleka, L.A., C. Vagias and V. Roussis. 2003. Natural products with anti-HIV activity from marine organisms. Curr. Top Med. Chem., 3(13): 1512-35. NOTA / NOTE: Valderrama, K. 2009. Evaluación de la oferta natural y potencial de producción de (+)-discodermólido y/o análogos de la esponja marina del Caribe colombiano Discodermia dissoluta. Tesis M. Sc. Química, Univ. Nacional de Colombia, Bogotá. 104 p. Valderrama, K., L. Castellanos and S. Zea. 2010. Validation and evaluation of an HPLC methodology for the quantification of the potent antimitotic Heteropods (Gastropoda: Pterotracheoidea) identified along a coastal-oceanic compound (+)-discodermolide in the Caribbean marine sponge Discodermia dissoluta. J. Sep. Sci., 33(15): 2316-21. transect in the Colombian Pacific Van Treeck, P., M. Eisinger, J. Müller, M. Paster and H. Schuhmacher. 2003. Mariculture trials with Mediterranean sponge species: the exploitation of an old natural resource with sustainable and novel methods. Aquaculture, 218:439–455. -
Invertebrate Collection Donated by Professor Dr. Ion Cantacuzino To
Travaux du Muséum National d’Histoire Naturelle «Grigore Antipa» Vol. 59 (1) pp. 7–30 DOI: 10.1515/travmu-2016-0013 Research paper Invertebrate Collection Donated by Professor Dr. Ion Cantacuzino to “Grigore Antipa” National Museum of Natural History from Bucharest Iorgu PETRESCU*, Ana–Maria PETRESCU ”Grigore Antipa” National Museum of Natural History, 1 Kiseleff Blvd., 011341 Bucharest 1, Romania. *corresponding author, e–mail: [email protected] Received: November 16, 2015; Accepted: April 18, 2016; Available online: June 28, 2016; Printed: June 30, 2016 Abstract. The catalogue of the invertebrate collection donated by Prof. Dr. Ion Cantacuzino represents the first detailed description of this historical act. The early years of Prof. Dr. Ion Cantacuzino’s career are dedicated to natural sciences, collecting and drawing of marine invertebrates followed by experimental studies. The present paper represents gathered data from Grigore Antipa 1931 inventory, also from the original handwritten labels. The specimens were classified by current nomenclature. The present donation comprises 70 species of Protozoa, Porifera, Coelenterata, Mollusca, Annelida, Bryozoa, Sipuncula, Arthropoda, Chaetognatha, Echinodermata, Tunicata and Chordata.. The specimens were collected from the North West of the Mediterranean Sea (Villefranche–sur–Mer) and in 1899 were donated to the Museum of Natural History from Bucharest. The original catalogue of the donation was lost and along other 27 specimens. This contribution represents an homage to Professor’s Dr. Cantacuzino generosity and withal restoring this donation to its proper position on cultural heritage hallway. Key words. Ion Cantacuzino, donation, collection, marine invertebrates, Mediterranean Sea, Villefranche–sur–Mer, France. INTRODUCTION The name of Professor Dr. -
Includes Abstracts of the
Number 65 (August 2015) The Malacologist Page 1 NUMBER 65 AUGUST 2015 Contents EDITORIAL …………………………….. ............................2 ANNUAL GENERAL MEETING—SPRING 2015 Annual Report of Council ...........................................................21 NOTICES ………………………………………………….2 Election of officers ………………………………………….....24 RESEARCH GRANT REPORTS Molecular phylogeny of Chaetodermomorpha (=Caudofoveata) EUROMOL CONFERENCE Programme in retrospect ……………………………………….….25 (Mollusca). Conference Abstracts - Oral presentations………………….....26 Nina Mikkelsen …………………………….………………..4 - Poster presentations ……………...…..53 The Caribbean shipworm Teredothyra dominicensis (Bivalvia, Teredinidae) has invaded and established breeding populations FORTHCOMING MEETINGS …………………………….…..... 72 in the Mediterranean Sea. Molluscan Forum .......................................................................72 J. Reuben Shipway, Luisa Borges, Johann Müller GRANTS AND AWARDS OF THE SOCIETY.............................76 & Simon Cragg ……………………………………………….7 MEMBERSHIP NOTICES ………………………………………....77 ANNUAL AWARD Evolution of chloroplast sequestration in Sacoglossa (Gastropoda, Heterobranchia) Gregor Christa ...……………………………………………....10 AGM CONFERENCE Programme in retrospect Planktic Gastropods ……………...….12 Conference Abstracts - Oral presentations………………….....13 - Poster presentations …………….....…18 Includes abstracts of the .. Images from The heart of a dragon: extraordinary circulatory system of the scaly-foot gastropod revealed Chong Chen, Jonathan Copley, Katrin Linse, -
Fossil-Calibrated Molecular Phylogeny of Atlantid Heteropods (Gastropoda, Pterotracheoidea)
Preprint: Please note that this article has not completed peer review. Fossil-calibrated molecular phylogeny of atlantid heteropods (Gastropoda, Pterotracheoidea) CURRENT STATUS: UNDER REVIEW Deborah Wall-Palmer Naturalis Biodiversity Center [email protected] Author ORCiD: https://orcid.org/0000-0003-2356-6122 Arie W Janssen Naturalis Biodiversity Center Erica Goetze University of Hawai'i at Manoa Le Qin Choo Naturalis Biodiversity Center Lisette Mekkes Naturalis Biodiversity Center Katja T. C. A. Peijnenburg Naturalis Biodiversity Center DOI: 10.21203/rs.3.rs-18183/v1 SUBJECT AREAS Evolutionary Biology KEYWORDS Atlantidae, Planktonic gastropods, cytochrome c oxidase subunit 1, 28S and 18S ribosomal rRNA, ocean change, rapid diversification 1 Abstract The aragonite shelled, planktonic gastropod family Atlantidae (shelled heteropods) is likely to be one of the first groups to be impacted by imminent ocean changes, including ocean warming and ocean acidification. With a fossil record spanning at least 100 Million years (Ma), atlantids have experienced and survived global-scale ocean changes and extinction events in the past. However, the diversification patterns and tempo of evolution in this family are largely unknown. Based on a concatenated maximum likelihood phylogeny of three genes (cytochrome c oxidase subunit 1 mitochondrial DNA, 28S and 18S ribosomal rRNA) we show that the three extant genera of the family Atlantidae, Atlanta, Protatlanta and Oxygyrus, form monophyletic clades. The genus Atlanta is split into two groups, one exhibiting smaller, well ornamented shells, and the other having larger, less ornamented shells. The fossil record, in combination with a fossil-calibrated phylogeny suggest that large scale atlantid extinction was accompanied by considerable and rapid diversification over the last 25 Ma, potentially driven by vicariance events.