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High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project
High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project AEA Technology, Environment Contract: W/35/00632/00/00 For: The Department of Trade and Industry New & Renewable Energy Programme Report issued 30 August 2002 (Version with minor corrections 16 September 2002) Keith Hiscock, Harvey Tyler-Walters and Hugh Jones Reference: Hiscock, K., Tyler-Walters, H. & Jones, H. 2002. High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project. Report from the Marine Biological Association to The Department of Trade and Industry New & Renewable Energy Programme. (AEA Technology, Environment Contract: W/35/00632/00/00.) Correspondence: Dr. K. Hiscock, The Laboratory, Citadel Hill, Plymouth, PL1 2PB. [email protected] High level environmental screening study for offshore wind farm developments – marine habitats and species ii High level environmental screening study for offshore wind farm developments – marine habitats and species Title: High Level Environmental Screening Study for Offshore Wind Farm Developments – Marine Habitats and Species Project. Contract Report: W/35/00632/00/00. Client: Department of Trade and Industry (New & Renewable Energy Programme) Contract management: AEA Technology, Environment. Date of contract issue: 22/07/2002 Level of report issue: Final Confidentiality: Distribution at discretion of DTI before Consultation report published then no restriction. Distribution: Two copies and electronic file to DTI (Mr S. Payne, Offshore Renewables Planning). One copy to MBA library. Prepared by: Dr. K. Hiscock, Dr. H. Tyler-Walters & Hugh Jones Authorization: Project Director: Dr. Keith Hiscock Date: Signature: MBA Director: Prof. S. Hawkins Date: Signature: This report can be referred to as follows: Hiscock, K., Tyler-Walters, H. -
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. -
Ringiculid Bubble Snails Recovered As the Sister Group to Sea Slugs
www.nature.com/scientificreports OPEN Ringiculid bubble snails recovered as the sister group to sea slugs (Nudipleura) Received: 13 May 2016 Yasunori Kano1, Bastian Brenzinger2,3, Alexander Nützel4, Nerida G. Wilson5 & Accepted: 08 July 2016 Michael Schrödl2,3 Published: 08 August 2016 Euthyneuran gastropods represent one of the most diverse lineages in Mollusca (with over 30,000 species), play significant ecological roles in aquatic and terrestrial environments and affect many aspects of human life. However, our understanding of their evolutionary relationships remains incomplete due to missing data for key phylogenetic lineages. The present study integrates such a neglected, ancient snail family Ringiculidae into a molecular systematics of Euthyneura for the first time, and is supplemented by the first microanatomical data. Surprisingly, both molecular and morphological features present compelling evidence for the common ancestry of ringiculid snails with the highly dissimilar Nudipleura—the most species-rich and well-known taxon of sea slugs (nudibranchs and pleurobranchoids). A new taxon name Ringipleura is proposed here for these long-lost sisters, as one of three major euthyneuran clades with late Palaeozoic origins, along with Acteonacea (Acteonoidea + Rissoelloidea) and Tectipleura (Euopisthobranchia + Panpulmonata). The early Euthyneura are suggested to be at least temporary burrowers with a characteristic ‘bubble’ shell, hypertrophied foot and headshield as exemplified by many extant subtaxa with an infaunal mode of life, while the expansion of the mantle might have triggered the explosive Mesozoic radiation of the clade into diverse ecological niches. The traditional gastropod subclass Euthyneura is a highly diverse clade of snails and slugs with at least 30,000 living species1,2. -
Sexual Conflict in Hermaphrodites
Downloaded from http://cshperspectives.cshlp.org/ on October 1, 2021 - Published by Cold Spring Harbor Laboratory Press Sexual Conflict in Hermaphrodites Lukas Scha¨rer1, Tim Janicke2, and Steven A. Ramm3 1Evolutionary Biology, Zoological Institute, University of Basel, 4051 Basel, Switzerland 2Centre d’E´cologie Fonctionnelle et E´volutive, CNRS UMR 5175, 34293 Montpellier Cedex 05, France 3Evolutionary Biology, Bielefeld University, 33615 Bielefeld, Germany Correspondence: [email protected] Hermaphrodites combine the male and female sex functions into a single individual, either sequentially or simultaneously. This simple fact means that they exhibit both similarities and differences in the way in which they experience, and respond to, sexual conflict compared to separate-sexed organisms. Here, we focus on clarifying how sexual conflict concepts can be adapted to apply to all anisogamous sexual systems and review unique (or especially im- portant) aspects of sexual conflict in hermaphroditic animals. These include conflicts over the timing of sex change in sequential hermaphrodites, and in simultaneous hermaphrodites, over both sex roles and the postmating manipulation of the sperm recipient by the sperm donor. Extending and applying sexual conflict thinking to hermaphrodites can identify general evolutionary principles and help explain some of the unique reproductive diversity found among animals exhibiting this widespread but to date understudied sexual system. onceptual and empirical work on sexual strategy of making more but smaller gam- Cconflict is dominated by studies on gono- etes—driven by (proto)sperm competition— chorists (species with separate sexes) (e.g., Par- likely forced the (proto)female sexual strategy ker 1979, 2006; Rice and Holland 1997; Holland into investing more resources per gamete (Par- and Rice 1998; Rice and Chippindale 2001; ker et al. -
A Biotope Sensitivity Database to Underpin Delivery of the Habitats Directive and Biodiversity Action Plan in the Seas Around England and Scotland
English Nature Research Reports Number 499 A biotope sensitivity database to underpin delivery of the Habitats Directive and Biodiversity Action Plan in the seas around England and Scotland Harvey Tyler-Walters Keith Hiscock This report has been prepared by the Marine Biological Association of the UK (MBA) as part of the work being undertaken in the Marine Life Information Network (MarLIN). The report is part of a contract placed by English Nature, additionally supported by Scottish Natural Heritage, to assist in the provision of sensitivity information to underpin the implementation of the Habitats Directive and the UK Biodiversity Action Plan. The views expressed in the report are not necessarily those of the funding bodies. Any errors or omissions contained in this report are the responsibility of the MBA. February 2003 You may reproduce as many copies of this report as you like, provided such copies stipulate that copyright remains, jointly, with English Nature, Scottish Natural Heritage and the Marine Biological Association of the UK. ISSN 0967-876X © Joint copyright 2003 English Nature, Scottish Natural Heritage and the Marine Biological Association of the UK. Biotope sensitivity database Final report This report should be cited as: TYLER-WALTERS, H. & HISCOCK, K., 2003. A biotope sensitivity database to underpin delivery of the Habitats Directive and Biodiversity Action Plan in the seas around England and Scotland. Report to English Nature and Scottish Natural Heritage from the Marine Life Information Network (MarLIN). Plymouth: Marine Biological Association of the UK. [Final Report] 2 Biotope sensitivity database Final report Contents Foreword and acknowledgements.............................................................................................. 5 Executive summary .................................................................................................................... 7 1 Introduction to the project .............................................................................................. -
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. -
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. -
Chec List Mollusca, Nudibranchia
ISSN 1809-127X (online edition) © 2011 Check List and Authors Chec List Open Access | Freely available at www.checklist.org.br Journal of species lists and distribution N Mollusca, Nudibranchia: New records and southward range extensions in Santa Catarina, southern Brazil ISTRIBUTIO 1* 2 3 3 D Vinicius Padula , Juliana Bahia , Camila Vargas and Alberto Lindner RAPHIC 1 Zoologische Staatssammlung München, Mollusca Sektion, Münchhausenstr. 21, 81247, München, Germany G 2 Universidade Federal do Rio de Janeiro, Departamento de Biologia Marinha, Laboratório de Benthos, Ilha do Fundão. CEP 21949-900. Rio de EO Janeiro, RJ, Brazil. G N O Brazil. *3 CorrespondingUniversidade Federal author: de E-mail: Santa Catarina,[email protected] Departamento de Ecologia e Zoologia – CCB, Edifício Fritz Muller. CEP 88040-970. Florianópolis, SC, OTES N Abstract: Nudibranch molluscs constitute a group of marine gastropods little studied in most of the Brazilian coast extension. Up to date, only ten species are known from Santa Catarina state, southern Brazil. This work presents four new records of nudibranchs from this region: Aeolidiella indica Bergh, 1988; Berghia rissodominguezi Muniain and Ortea, 1999; Chromodoris paulomarcioi Domínguez, García and Troncoso, 2006 and Tambja stegosauriformis Pola, Cervera, and Gosliner, 2005, expanding the known geographic distribution of the last two species more than 900 km southward. The Santa Catarina state, southern Brazil (26–29° S), Chiaje, 1823), by Pimpão and Magalhães (2004). In represents the southernmost limit of rocky shores in the 2006, the dorid Hypselodoris lajensis Troncoso, García tropical Southwest Atlantic (Floeter et al. 2008). Yet, the and Urgorri, 1998 was reported to the Arvoredo Marine marginal reef sites in the region have only recently started Biological Reserve (Domínguez et al. -
Twelve Invertebrate and Eight Fish Species New to the Marine Fauna of Madeira, and a Discussion of the Zoogeography of the Area
HELGOL.~NDER MEERESUNTERSUCHUNGEN Helgol~inder Meeresunters. 52, 197-207 (1998) Twelve invertebrate and eight fish species new to the marine fauna of Madeira, and a discussion of the zoogeography of the area Peter Wirtz Centro de Ci~ncias Biol6gicas e Geol6gicas, Universidade da Madeira, Largo do Col~gio, P - 9000 Funchal, Portugal, Madeira ABSTRACT: The benthic ctenophore Vallicula multiformis, a large undescribed flatworm species of the genus Pseudoceros, the prosobranch gastropod Tonna maculosa, the opisthobranch gastropods Placida cf. dendritica, Calona elegans, Aeolidiella sanguinea, Janolus cristatus, the decapod Balssia gasti, the sea urchin Schizaster canaliferus and the tunicates Cla velina lepa diformis, Cla velina della- vallei and Pycnoclavella taureanensis are recorded from Madeira for the first time. This is the first record of a platyctenid ctenophore in the eastern Atlantic. The teleost fishes Pomatoschistus pictus, Vaneaugobius canariensis, Chromogobius sp., Nerophis ophidion, Hippocampus hippocampus, Acanthocybium solandri, Sphyraena viridensis and Sphyraena barracuda are recorded from Ma- deira for the first time. The presence of the sea-hare Aplysia dactylomela at Madeira is confirmed; the species has increased tremendously in abundance in the last four years. The crocodile fish Gram- moplites gruveli can occasionally be found in the mantle cavity of cuttlefish (Sepia officinalis) sold at the fish market of Funchal, but does not originate from Madeiran waters. An analysis of 100 new records from the coastal fauna of Madeira shows that, while predominantly of lusitanian, medi- terranean and mauritanian affinity, Madeira's shallow water fauna contains a large component of tropical species. INTRODUCTION During an ongoing survey of the larger marine vertebrates and invertebrates of the coasts of Madeira {Biscoito & Wirtz, 1994; Wirtz, 1994, 1995a, 1995b; Wittmann & Wirtz, in press), several species were encountered that apparently had not yet been recorded from Madeira. -
Incorporated Nematocysts in Aeolidiella
Toxicon 60 (2012) 1108–1116 Contents lists available at SciVerse ScienceDirect Toxicon journal homepage: www.elsevier.com/locate/toxicon Incorporated nematocysts in Aeolidiella stephanieae (Gastropoda, Opisthobranchia, Aeolidoidea) mature by acidification shown by the pH sensitive fluorescing alkaloid Ageladine A Dana Obermann a, Ulf Bickmeyer b, Heike Wägele a,* a Zoologisches Forschungsmuseum Alexander Koenig, Adenauerallee 160, 53113 Bonn, Germany b Alfred-Wegener-Institut für Polar und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany article info abstract Article history: The sequestration of nematocysts (a special group of cnidocysts) from cnidarian prey with Received 16 May 2012 subsequent use in defence is described for few metazoan phyla. Members of the taxon Received in revised form 2 August 2012 Aeolidoidea (Nudibranchia, Gastropoda) are well-known for this. Questions regarding the Accepted 7 August 2012 reasons some nematocysts do not discharge when the gastropod feeds and how these Available online 14 August 2012 same nematocysts can be transported along the digestive tract into specialized morpho- logical structures called cnidosacs, remain unanswered. Within the cnidosac, nematocysts Keywords: are incorporated in cells and finally be used for defence against predators. Nudibranchia Nematocysts The most plausible explanation for this phenomenon suggests there are immature and Cnidosac therefore non-functional nematocysts in the food. A recent study by Berking and Kleptocnides Herrmann (2005) on cnidarians suggested that the nematocysts mature by acidification Defence via proton transfer into the nematocyst capsule. According to this hypothesis only Ageladine A immature nematocysts are transported into the cnidosac where they are then made functional through an accumulation of protons. In this study we present a fluorescence staining method that tests the hypothesis by Berking and Herrmann (2005) and detects changes in the pH values of incorporated nematocysts, interpreted as changes in matu- ration stages. -
Boletin 20 NUEVO 4/9/06 12:34 Página 1
Boletin 20 NUEVO 4/9/06 12:34 Página 1 BOLETÍN INSTITUTO ESPAÑOL DE OCEANOGRAFÍA An annotated and updated checklist of the opisthobranchs (Mollusca: Gastropoda) from Spain and Portugal (including islands and archipelagos) J. L. Cervera1, G. Calado2,3, C. Gavaia2,4*, M. A. E. Malaquias2,5, J. Templado6, M. Ballesteros7, J. C. García-Gómez8 and C. Megina1 1Departamento de Biología 5Mollusca Research Group Facultad de Ciencias del Mar y Ambientales Department of Zoology Universidad de Cádiz The Natural History Museum Polígono Río San Pedro, s/n Cromwell Road Apdo. 40, E-11510 Puerto Real, Cádiz, Spain. London SW7 5BD, United Kingdom E-mail: [email protected] 6Museo Nacional de Ciencias Naturales (CSIC) 2Instituto Português de Malacologia José Gutiérrez Abascal 2 Zoomarine E-28006 Madrid, Spain E. N. 125 km 65 Guia, P-8200-864 Albufeira, Portugal 7Departamento de Biología Animal Facultad de Biología 3Centro de Modelação Ecológica Imar Universidad de Barcelona FCT/UNL Avda. Diagonal 645 Quinta da Torre E-08028 Barcelona, Spain P-2825-114 Monte da Caparica, Portugal 8Laboratorio de Biología Marina 4Centro de Ciências do Mar Departamento de Fisiología y Zoología Faculdade de Ciências do Mar e do Ambiente Facultad de Biología Universidade do Algarve Universidad de Sevilla Campus de Gambelas Avda. Reina Mercedes 6 P-8000-010 Faro, Portugal Apdo. 1095, E-41012 Sevilla, Spain *César Gavaia died on 3rd July 2003, in a car accident Received January 2004. Accepted December 2004 ISSN: 0074-0195 MINISTERIO INSTITUTO ESPAÑOL DE EDUCACIÓN DE OCEANOGRAFÍA Y CIENCIA Vol. 20 · Núms. 1-4 Págs. 1-122 Edita (Published by): INSTITUTO ESPAÑOL DE OCEANOGRAFÍA Avda. -
The Chemistry and Chemical Ecology of Nudibranchs Cite This: Nat
Natural Product Reports View Article Online REVIEW View Journal | View Issue The chemistry and chemical ecology of nudibranchs Cite this: Nat. Prod. Rep.,2017,34, 1359 Lewis J. Dean and Mich`ele R. Prinsep * Covering: up to the end of February 2017 Nudibranchs have attracted the attention of natural product researchers due to the potential for discovery of bioactive metabolites, in conjunction with the interesting predator-prey chemical ecological interactions that are present. This review covers the literature published on natural products isolated from nudibranchs Received 30th July 2017 up to February 2017 with species arranged taxonomically. Selected examples of metabolites obtained from DOI: 10.1039/c7np00041c nudibranchs across the full range of taxa are discussed, including their origins (dietary or biosynthetic) if rsc.li/npr known and biological activity. Creative Commons Attribution-NonCommercial 3.0 Unported Licence. 1 Introduction 6.5 Flabellinoidea 2 Taxonomy 6.6 Tritonioidea 3 The origin of nudibranch natural products 6.6.1 Tethydidae 4 Scope of review 6.6.2 Tritoniidae 5 Dorid nudibranchs 6.7 Unassigned families 5.1 Bathydoridoidea 6.7.1 Charcotiidae 5.1.1 Bathydorididae 6.7.2 Dotidae This article is licensed under a 5.2 Doridoidea 6.7.3 Proctonotidae 5.2.1 Actinocyclidae 7 Nematocysts and zooxanthellae 5.2.2 Cadlinidae 8 Conclusions 5.2.3 Chromodorididae 9 Conicts of interest Open Access Article. Published on 14 November 2017. Downloaded 9/28/2021 5:17:27 AM. 5.2.4 Discodorididae 10 Acknowledgements 5.2.5 Dorididae 11