Page 1 Contents • Welcome Page 2

Total Page:16

File Type:pdf, Size:1020Kb

Page 1 Contents • Welcome Page 2 Contents • Welcome Page 2 • International Steering & Local Organising Committee Page 2 • Sponsors Page 3 • Sponsors Ads Page 4 • General Information Page 10 • Health & Safety Page 11 • Conference Programme Page 13 • Additional Side Meetings Page 21 • Social Events & Exhibition Page 22 • Excursion Suggestions Page 23 • Oral Abstracts (alpha order by author surname) Page 25 • Poster Listing Page 171 • Poster Abstracts (alpha order by author surname) Page 185 • List of Participants Page 251 • Maps of Te Papa Page 256 • Map of Wellington Page 258 Conference Secretariat Conferences & Events Ltd PO Box 24078 Manners Street, Wellington Tel: +64 (0)4 384 1511 Web: www.confer.co.nz Page 1 Welcome Welcome to Wellington, New Zealand and the 13th International Deep-Sea Biology Symposium. This is the first time that the symposium has been held in the Southern Hemisphere and it is encouraging, in these difficult financial times, that so many of you have made the long journey to take part in the meeting. The hope is that this meeting will maintain the success of the previous gatherings of deep-sea scientists, and representatives of government, non-government organisations, and industry — where the results of the latest research are exchanged and discussed, particularly with a view as to how this information can be used to effectively manage the increasing pressure placed on deep-sea ecosystems by human activities. On offer at this symposium is a wide array of oral and poster presentations, which I’m sure, will contribute to this goal. As well as engaging fully with the presentations and resulting discussions I hope that you will also enjoy the food and drink that is provided to fuel these activities, as well as take time in the evenings and Wednesday afternoon to explore the “coolest little capital in the world” and its surrounds. Finally, I wish to thank members of the International Steering Committee and the Local Organising Committee for all their enthusiastic and valuable advice, input and labours. Louise Watson, the symposium manager from Conference & Events Ltd, deserves particular recognition for making things happen. My original co-convener, Mireille Consalvey, provided a mass of good ideas and energy at the outset of the symposium organisation — without her contribution this symposium would not have gotten off the ground. Special thanks are also owed to all the symposium sponsors — for without their financial contribution this symposium would not have been possible at all. Here’s to a productive and fun symposium. Ashley Rowden Symposium Convener International Steering Committee Maria Baker, University of Southampton, UK Antje Boetius, AWI, Germany Hiroshi Kitazato, JAMSTEC, Japan Lenaick Menot, IFREMER, France Ashley Rowden, NIWA, New Zealand Thomas Schlacher, University of Sunshine Coast, Australia Javier Sellanes, University Catolica Norte/ COPAS - University Concepcion, Chile Craig Smith, University of Hawaii, USA Andrew Thurber, Oregon State University, USA Local Organising Committee Jennifer Beaumont, Rachel Boschen, David Bowden, Malcolm Clark, Matthew Dunn, Dennis Gordon, Daniel Leduc, Anne-Nina Loerz, Erika Mackay, Els Maas, Scott Nodder, Peter "Chazz" Marriott, Matt Pinkerton, Ashley Rowden, Kareen Schnabel, Di Tracey, NIWA Mark Costello, University of Auckland Simon Davy, Victoria University of Wellington Conrad Pilditch, University of Waikato Keith Probert, University of Otago Andrew Stewart, Rick Webber, Museum of New Zealand Te Papa Tongarewa Page 2 Sponsors The 13th Deep-Sea Biology Symposium Organising Committee wishes to acknowledge the generous support of our sponsors: Sponsors of: Sponsors of: Conservation & Management Session Sponsors of: Discovery Session Sponsors of: Biodiversity Session Sponsors of: Earthship Productions Sponsors of: Trench Session Page 3 Intteridge Ad COLOUR PAGE Page 4 NIWA Ad COLOUR PAGE Page 5 MBIE Ad COLOUR PAGE Page 6 PEW Ad 1 COLOUR PAGE Page 7 Pew Ad 2 COLOUR PAGE Page 8 MPI Ad COLOUR PAGE Page 9 General Information Registration and Information Desk Registration desk phone: 021 225 0337 The registration and information desk will be located in Oceania on level 3 of Te Papa from Sunday 2nd December at 15.00hrs until 17.00hrs on Friday 7th December, during the conference between the hours listed below: • Sunday 2nd December 15.00 – 17.00 • Monday 3rd December 08.00 – 17.00 • Tuesday 4th December 08.00 – 17.00 • Wednesday 5th December 08.00 – 17.00 • Thursday 6th December 08.00 – 17.00 • Friday 7th December 08.00 – 17.00 The following information is offered to make your attendance at the conference as pleasant and trouble-free as possible. If you require help, please call at the registration desk and we will do everything we can to assist you. Accommodation For those registrants who have reserved accommodation through Conference & Events, please ensure accounts are settled in full on departure, including all meals, telephone calls and mini bar charges. No accounts can be charged to the 13th Deep-Sea Biology Symposium Doctors and Pharmacies • City Medical Centre Level 1, 10 Brandon Street, phone 471 2161 8am – 6pm weekdays • After Hours Medical Centre 17 Adelaide Road, Newtown, phone 384 4944 8am – 11pm every day (no appointment necessary) Health and Safety Emergency Procedures • General Emergency For fire, ambulance or police, dial 1 for an outside line, then 111. • Fire If you discover a fire or hear continuous ringing of the fire alarm, leave the building immediately and assemble outside the building as instructed by Te Papa Hosts. • Earthquake In the event of an earthquake, please remain in the building. Move away from any windows or equipment that may fall and take immediate shelter under, or close to, solid furniture such as tables or desks. If no furniture is available, drop to your knees, with your back to windows, clasp both hands firmly behind your head and bury your head in your hands. Most importantly, keep calm. Page 10 • Evacuation The continuous sounding of an alarm will indicate that the building is to be evacuated. When the alarm is activated, all magnetically locked doors will be released, making emergency escape routes available for use. Leave the building immediately, using the nearest stairway or exit. Messages The message board will be located by the registration desk in Oceania on Level 3 of Te Papa. Mobile Phones and Pagers Mobile phones and pagers must be turned off (or set to vibrate) while sessions are in progress. Name Badges As a security requirement, we request that participants wear their conference name badges to all sessions and refreshment breaks. Please return these for recycling, along with your lanyard to the registration desk at the conclusion of the conference. Oral Presentations If you are using PowerPoint you have been requested to email your presentation prior to the conference. If you were unable to do this, please hand in your presentation on a USB stick to the AV technician at the information desk as soon as possible. Chairpersons of sessions are asked to be present at least five minutes before the session starts so that speakers can introduce themselves. All speakers are requested to remain within their allocated time (including time for questions from the audience if wanted). Parking Te Papa’s car park is open 24 hours, 7 days a week. A special discounted conference rate of $9 per day is available for delegates. After you park your car, please ask for the discounted ticket before departing from the registration desk staff in Oceania. Car parking charges (if you don’t need to stay for the day) • 15 min–1 hour $3.5 • 1–2 hours $7 Anything over 2 hours is charged at $10 so it would be in your interest to request a discounted parking ticket from registration desk staff in Oceania. Posters / Poster Session All posters are located in Oceania on level 3 of Te Papa. Please hang your poster (using the Velcro provided) by your poster number (which was communicated to you via email prior to the conference). Poster numbers are also in the poster section of this handbook. Please ensure you poster is hung up when you first arrive at the conference. The Poster Session will take place on Monday 3rd December from 17.00 hrs – 19.00 hrs; we ask that you stand by your board at this time to answer questions. Drinks and canapés will be served during this time. Public Transport The Airport Flyer is an express bus service that runs into central Wellington every 20 minutes during the day and every 30 minutes in the evenings. It costs $6.50 each way. Page 11 The Airport Flyer departs from the southern end of the airport terminal, Level 0 (exit from baggage claim doors on Level 0 and turn right) past the Airport Flyer waiting area. The timetable for the Airport Flyer is available at www.metlink.org.nz (select the timetable for Route 91 – Airport Flyer). Smoking Te Papa is a smoke-free venue (including outdoor areas, such as balconies). Smokers are requested to smoke outside the premises of Te Papa. Storage of Luggage Storage of luggage on departure date can be arranged through the hotel concierge for those staying at the conference hotels. For all other delegates, luggage can be stored with the Conference Secretariat staff at the registration desk. Taxis/Shuttles • Wellington Combined Taxis (ph 0800 38 44 44) • Corporate Cabs (ph 04 387 4600) • Cooperative Shuttles (ph 04 387 8787) When booking a taxi or shuttle, the street address for the conference venue is: Te Papa, Wakefield Street Teas and Lunches Teas and lunches will be served in Oceania on level 3 of Te Papa. If you have specified a dietary requirement when completing the online registration, this will have been passed on to the venue and will be available for you. Please make yourself known to catering staff.
Recommended publications
  • The Status of Natural Resources on the High-Seas
    The status of natural resources on the high-seas Part 1: An environmental perspective Part 2: Legal and political considerations An independent study conducted by: The Southampton Oceanography Centre & Dr. A. Charlotte de Fontaubert The status of natural resources on the high-seas i The status of natural resources on the high-seas Published May 2001 by WWF-World Wide Fund for Nature (Formerly World Wildlife Fund) Gland, Switzerland. Any reproduction in full or in part of this publication must mention the title and credit the above mentioned publisher as the copyright owner. The designation of geographical entities in this book, and the presentation of the material, do not imply the expression of any opinion whatsoever on the part of WWF or IUCN concerning the legal status of any country, territory, or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. The views expressed in this publication do not necessarily reflect those of WWF or IUCN. Published by: WWF International, Gland, Switzerland IUCN, Gland, Switzerland and Cambridge, UK. Copyright: © text 2001 WWF © 2000 International Union for Conservation of Nature and Natural Resources © All photographs copyright Southampton Oceanography Centre Reproduction of this publication for educational or other non-commercial purposes is authorized without prior written permission from the copyright holder provided the source is fully acknowledged. Reproduction of this publication for resale or other commercial purposes is prohibited without prior written permission of the copyright holder. Citation: WWF/IUCN (2001). The status of natural resources on the high-seas. WWF/IUCN, Gland, Switzerland. Baker, C.M., Bett, B.J., Billett, D.S.M and Rogers, A.D.
    [Show full text]
  • Phylum MOLLUSCA Chitons, Bivalves, Sea Snails, Sea Slugs, Octopus, Squid, Tusk Shell
    Phylum MOLLUSCA Chitons, bivalves, sea snails, sea slugs, octopus, squid, tusk shell Bruce Marshall, Steve O’Shea with additional input for squid from Neil Bagley, Peter McMillan, Reyn Naylor, Darren Stevens, Di Tracey Phylum Aplacophora In New Zealand, these are worm-like molluscs found in sandy mud. There is no shell. The tiny MOLLUSCA solenogasters have bristle-like spicules over Chitons, bivalves, sea snails, sea almost the whole body, a groove on the underside of the body, and no gills. The more worm-like slugs, octopus, squid, tusk shells caudofoveates have a groove and fewer spicules but have gills. There are 10 species, 8 undescribed. The mollusca is the second most speciose animal Bivalvia phylum in the sea after Arthropoda. The phylum Clams, mussels, oysters, scallops, etc. The shell is name is taken from the Latin (molluscus, soft), in two halves (valves) connected by a ligament and referring to the soft bodies of these creatures, but hinge and anterior and posterior adductor muscles. most species have some kind of protective shell Gills are well-developed and there is no radula. and hence are called shellfish. Some, like sea There are 680 species, 231 undescribed. slugs, have no shell at all. Most molluscs also have a strap-like ribbon of minute teeth — the Scaphopoda radula — inside the mouth, but this characteristic Tusk shells. The body and head are reduced but Molluscan feature is lacking in clams (bivalves) and there is a foot that is used for burrowing in soft some deep-sea finned octopuses. A significant part sediments. The shell is open at both ends, with of the body is muscular, like the adductor muscles the narrow tip just above the sediment surface for and foot of clams and scallops, the head-foot of respiration.
    [Show full text]
  • Geobio-Center LMU Report 2014 / 2015
    GeoBio-Center LMU LMU ReportGeoBio-Center 2014 / 2015 Report 2012 / 2013 GeoBio-CenterLMU Report 2014 / 2015 Editor: Dirk Erpenbeck, Angelo Poliseno Layout: Lydia Geißler Cover composition: Lydia Geißler GeoBio-Center LMU, Richard-Wagner-Str. 10, 80333 München http://www.geobio-center.uni-muenchen.de Contents Welcoming note ......................................................................................................................4 Achievements of the GeoBio-Center LMU members 2014 & 2015 at a glance ......................5 Members of the GeoBio-CenterLMU ........................................................................................6 Memorial to Alexander Volker Altenbach (1953-2015) ..........................................................9 Publications in ISI-indexed Journals ...................................................................................14 Other peer-reviewed Publications .......................................................................................21 Further Publications .............................................................................................................23 Grants and Stipends ............................................................................................................26 Honors and Awards ..............................................................................................................27 Presentations on Conferences and Symposia ....................................................................28 Teaching ................................................................................................................................35
    [Show full text]
  • An Isotope Approach
    Determining Cetacean – Cephalopod Trophic Interactions – An Isotope Approach By Christine Heather Jackson Bachelor of Arts, James Cook University Graduate Diploma (Health Promotion), Curtin University of Technology Master of Science, University of Tasmania Submitted in fulfilment of the requirements for the degree Doctor of Philosophy University of Tasmania (October 2016) ii DECLARATION This thesis contains no material which has been accepted for a degree or diploma by the University or any other institution, except by way of background information and duly acknowledged in the thesis, and to the best of my knowledge and belief no material previously published or written by another person except where due acknowledgement is made in the text of the thesis, nor does the thesis contain any material that infringes copyright Signed; _________________________________ Christine H. Jackson iii AUTHORITY OF ACCESS This thesis may be made available for loan and limited copying and communication in accordance with the Copyright Act 1968. Signed; _________________________________ Christine H. Jackson iv ABSTRACT Determining the biotic and abiotic influences on the distribution and abundance of marine mammals is essential for understanding the dynamics of the food chain. The predator-prey relationship can be deterministic in shaping both the community structure and function of marine ecosystems. This is especially pertinent to recovering toothed whale populations given their large size and high prey consumption rates. A greater knowledge of the trophic linkages between toothed whales and their prey will facilitate assessments of their combined impact on the ecosystem since marine food webs are a fusion of bottom-up and top-down energy and nutrient flow.
    [Show full text]
  • Publications Supported by NOAA's Office of Ocean Exploration And
    1 Publications Supported by NOAA’s Office of Ocean Exploration and Research Compiled by Chris Belter, NOAA Central Library Accurate as of 17 April 2012 Journal Articles (n=454) Ahyong ST. 2008. Deepwater crabs from seamounts and chemosynthetic habitats off eastern New Zealand (Crustacea : Decapoda : Brachyura). Zootaxa(1708):1-72. Aig D, Haywood K. 2008. Through the Sea Snow: The Central Role of Videography in the Deep Gulf Wrecks Mission. International Journal of Historical Archaeology 12(2):133-145. doi:10.1007/s10761-008-0049-7 Andrews AH, Stone RP, Lundstrom CC, DeVogelaere AP. 2009. Growth rate and age determination of bamboo corals from the northeastern Pacific Ocean using refined Pb-210 dating. Marine Ecology-Progress Series 397:173-185. doi:10.3354/meps08193 Angel MV. 2010. Towards a full inventory of planktonic Ostracoda (Crustacea) for the subtropical Northwestern Atlantic Ocean. Deep-Sea Research Part Ii-Topical Studies in Oceanography 57(24-26):2173-2188. doi:10.1016/j.dsr2.2010.09.020 Arellano SM, Young CM. 2009. Spawning, Development, and the Duration of Larval Life in a Deep-Sea Cold-Seep Mussel. Biological Bulletin 216(2):149-162. Auster PJ. 2007. Linking deep-water corals and fish populations. Bulletin of Marine Science 81:93-99. Auster PJ, Gjerde K, Heupel E, Watling L, Grehan A, Rogers AD. 2011. Definition and detection of vulnerable marine ecosystems on the high seas: problems with the "move-on" rule. ICES Journal of Marine Science 68(2):254-264. doi:10.1093/icesjms/fsq074 Auster PJ, Watling L. 2010. Beaked whale foraging areas inferred by gouges in the seafloor.
    [Show full text]
  • Chapter 51. Biological Communities on Seamounts and Other Submarine Features Potentially Threatened by Disturbance
    Chapter 51. Biological Communities on Seamounts and Other Submarine Features Potentially Threatened by Disturbance Contributors: J. Anthony Koslow, Peter Auster, Odd Aksel Bergstad, J. Murray Roberts, Alex Rogers, Michael Vecchione, Peter Harris, Jake Rice, Patricio Bernal (Co-Lead members) 1. Physical, chemical, and ecological characteristics 1.1 Seamounts Seamounts are predominantly submerged volcanoes, mostly extinct, rising hundreds to thousands of metres above the surrounding seafloor. Some also arise through tectonic uplift. The conventional geological definition includes only features greater than 1000 m in height, with the term “knoll” often used to refer to features 100 – 1000 m in height (Yesson et al., 2011). However, seamounts and knolls do not appear to differ much ecologically, and human activity, such as fishing, focuses on both. We therefore include here all such features with heights > 100 m. Only 6.5 per cent of the deep seafloor has been mapped, so the global number of seamounts must be estimated, usually from a combination of satellite altimetry and multibeam data as well as extrapolation based on size-frequency relationships of seamounts for smaller features. Estimates have varied widely as a result of differences in methodologies as well as changes in the resolution of data. Yesson et al. (2011) identified 33,452 seamount and guyot features > 1000 m in height and 138,412 knolls (100 – 1000 m), whereas Harris et al. (2014) identified 10,234 seamount and guyot features, based on a stricter definition that restricted seamounts to conical forms. Estimates of total abundance range to >100,000 seamounts and to 25 million for features > 100 m in height (Smith 1991; Wessel et al., 2010).
    [Show full text]
  • Biological Structures As a Source of Habitat Heterogeneity and Biodiversity on the Deep Ocean Margins Lene Buhl-Mortensen1, Ann Vanreusel2, Andrew J
    Marine Ecology. ISSN 0173-9565 SPECIAL TOPIC Biological structures as a source of habitat heterogeneity and biodiversity on the deep ocean margins Lene Buhl-Mortensen1, Ann Vanreusel2, Andrew J. Gooday3, Lisa A. Levin4, Imants G. Priede5,Pa˚ l Buhl-Mortensen1, Hendrik Gheerardyn2, Nicola J. King5 & Maarten Raes2 1 Institute of Marine Research, Benthic habitat group, Bergen, Norway 2 Ghent University, Marine Biology research group, Belgium 3 National Oceanography Centre Southampton, Southampton, UK 4 Integrative Oceanography Division, Scripps Institution of Oceanography, University of California, La Jolla, CA, USA 5 Oceanlab, University of Aberdeen, Newburgh, Aberdeenshire, UK Keywords Abstract Biodiversity; biotic structures; commensal; continental slope; deep sea; deep-water coral; Biological structures exert a major influence on species diversity at both local and ecosystem engineering; sponge reefs; regional scales on deep continental margins. Some organisms use other species as xenophyophores. substrates for attachment, shelter, feeding or parasitism, but there may also be mutual benefits from the association. Here, we highlight the structural attributes Correspondence and biotic effects of the habitats that corals, sea pens, sponges and xenophyo- Lene Buhl-Mortensen, Institute of Marine phores offer other organisms. The environmental setting of the biological struc- Research, Benthic habitat group, P.O. Box 1870 Nordnes, N-5817 Bergen, Norway tures influences their species composition. The importance of benthic species as E-mail: [email protected] substrates seems to increase with depth as the complexity of the surrounding geological substrate and food supply decline. There are marked differences in the Accepted: 30 December 2009 degree of mutualistic relationships between habitat-forming taxa. This is espe- cially evident for scleractinian corals, which have high numbers of facultative doi:10.1111/j.1439-0485.2010.00359.x associates (commensals) and few obligate associates (mutualists), and gorgonians, with their few commensals and many obligate associates.
    [Show full text]
  • Molecular Species Delimitation and Biogeography of Canadian Marine Planktonic Crustaceans
    Molecular Species Delimitation and Biogeography of Canadian Marine Planktonic Crustaceans by Robert George Young A Thesis presented to The University of Guelph In partial fulfilment of requirements for the degree of Doctor of Philosophy in Integrative Biology Guelph, Ontario, Canada © Robert George Young, March, 2016 ABSTRACT MOLECULAR SPECIES DELIMITATION AND BIOGEOGRAPHY OF CANADIAN MARINE PLANKTONIC CRUSTACEANS Robert George Young Advisors: University of Guelph, 2016 Dr. Sarah Adamowicz Dr. Cathryn Abbott Zooplankton are a major component of the marine environment in both diversity and biomass and are a crucial source of nutrients for organisms at higher trophic levels. Unfortunately, marine zooplankton biodiversity is not well known because of difficult morphological identifications and lack of taxonomic experts for many groups. In addition, the large taxonomic diversity present in plankton and low sampling coverage pose challenges in obtaining a better understanding of true zooplankton diversity. Molecular identification tools, like DNA barcoding, have been successfully used to identify marine planktonic specimens to a species. However, the behaviour of methods for specimen identification and species delimitation remain untested for taxonomically diverse and widely-distributed marine zooplanktonic groups. Using Canadian marine planktonic crustacean collections, I generated a multi-gene data set including COI-5P and 18S-V4 molecular markers of morphologically-identified Copepoda and Thecostraca (Multicrustacea: Hexanauplia) species. I used this data set to assess generalities in the genetic divergence patterns and to determine if a barcode gap exists separating interspecific and intraspecific molecular divergences, which can reliably delimit specimens into species. I then used this information to evaluate the North Pacific, Arctic, and North Atlantic biogeography of marine Calanoida (Hexanauplia: Copepoda) plankton.
    [Show full text]
  • Thaler Et Al. 2010
    Conservation Genet Resour (2010) 2:101–103 DOI 10.1007/s12686-010-9174-9 TECHNICAL NOTE Characterization of 12 polymorphic microsatellite loci in Ifremeria nautilei, a chemoautotrophic gastropod from deep-sea hydrothermal vents Andrew David Thaler • Kevin Zelnio • Rebecca Jones • Jens Carlsson • Cindy Lee Van Dover • Thomas F. Schultz Received: 28 December 2009 / Accepted: 1 January 2010 / Published online: 9 January 2010 Ó Springer Science+Business Media B.V. 2010 Abstract Ifremeria nautilei is deep-sea provannid gas- et al. 2008). Commercial grade polymetallic sulfide tropod endemic to hydrothermal vents at southwest Pacific deposits are often associated with hydrothermal vents, back-arc spreading centers. Twelve, selectively neutral and making some vents candidates for mining operations (Rona unlinked polymorphic microsatellite loci were developed 2003). Defining natural conservation units for key vent- for this species. Three loci deviated significantly from endemic organisms can inform best practices for mini- Hardy–Weinberg expectations. Average observed hetero- mizing the environmental impact of mining activities zygosity ranged from 0.719 to 0.906 (mean HO = 0.547, (Halfar and Fujita 2002). SD = 0.206). Three of the 12 loci cross-amplified in two Ifremeria nautilei is a deep-sea vent-endemic provannid species of Alviniconcha (Provannidae) that co-occur with I. gastropod from the western Pacific (Bouchet and Ware´n nautilei at Pacific vent habitats. Microsatellites developed 1991), where it is a dominant primary consumer at geo- for I. nautilei are being deployed to study connectivity graphically isolated back-arc basins (Desbruye`res et al. among populations of this species colonizing geographi- 2006). The species is dependent on chemoautotrophic cally discrete back-arc basin vent systems.
    [Show full text]
  • Zootaxa 1843: 57–66 (2008) ISSN 1175-5326 (Print Edition) ZOOTAXA Copyright © 2008 · Magnolia Press ISSN 1175-5334 (Online Edition)
    Zootaxa 1843: 57–66 (2008) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2008 · Magnolia Press ISSN 1175-5334 (online edition) Alicellidae and Valettiopsidae, two new callynophorate families (Crustacea: Amphipoda) J.K. LOWRY1 & C. DE BROYER2 1Crustacea Section, Australian Museum, 6 College Street, Sydney, NSW 2010, Australia. E-mail: [email protected] 2Royal Belgian Institue of Natural Sciences, Departement of Invertebrates (Carcinology), 29 Rue Vautier, B-1000 Bruxelles, Belgium. E-mail: [email protected] Abstract Two new families, the Alicellidae fam. nov. and the Valettiopsidae fam. nov., are described based on genera traditionally considered as lysianassoid amphipods. The Alicellidae fam. nov. are deep-sea scavengers often associated with thermal vents. They are distinguished from all other amphipods by a combination of characters which includes a callynophore on antenna 1; a broad, serrate left lacinia mobilis (occasionally narrow or vestigial) and a reduced or vestigial right lacinia mobilis (occasionally broad and serrate); simple or subchelate gnathopod 1; an elongate ischium, rectolinear carpus and propodus and a small dactylus on gnathopod 2 (not mitten-shaped); absence of apical robust setae on uropods 1 and 2 and a deeply cleft telson. The family contains 6 genera: Alicella Chevreux, 1899; Apotectonia Barnard & Ingram, 1990; Dia- tectonia Barnard & Ingram, 1990; Paralicella Chevreux, 1908; Tectovalopsis Barnard & Ingram, 1990; Transtectonia Barnard & Ingram, 1990. The Valettiopsidae fam. nov. are deep-sea scavenging amphipods defined by a combination of characters which includes a callynophore on antenna 1; serrate, curved incisors; a well developed, serrate lacinia mobilis on each mandible, an oblique setal row on the inner plate of maxilla 2, an elongate ischium on gnathopod 2; the absence of robust setae on the apices of uropods 1 and 2 and a deeply cleft telson.
    [Show full text]
  • The Appropriation Bill 2003
    SOUTH GEORGIA AND SOUTH SANDWICH ISLANDS GAZETTE PUBLISHED BY AUTHORITY No. 2 13 June 2013 The following are published in this Gazette – Notices 1 to 10; Supplementary Appropriation (2012) Ordinance 2013 (No 2 of 2013); Appropriation (2013) Ordinance 2013 (No 3 of 2013); Wildlife and Protected Areas (Amendment) Ordinance 2013 (No 4 of 2013); Postal Services (Amendment) Ordinance 2013 (No 5 of 2013); Marine Protected Areas Order 2013 (SR&O No 1 of 2013); Prohibited Areas Order 2013 (SR&O No 2 of 2013); and Coins Order 2013 (SR&O No 3 of 2013). 1 NOTICES terminated sooner. Dated 11 February 2013 No. 1 14 December 2012 N. R. HAYWOOD C.V.O., Commissioner. United Kingdom Statutory Instruments ____________________ Notice is hereby given that the following United Kingdom No. 3 6 May 2013 Statutory Instruments have been published in the United Kingdom by The Stationery Office Limited and are Police Ordinance 1967 available to view at www.legislation.gov.uk: section 5 Enrolment of Police Officer 2012 No 2748 – The Iraq (United Nations Sanctions) 1. The Police Ordinance 1967 (No 9 of 1967, Falkland (Overseas Territories) (Amendment) Order 2012; Islands) applies to South Georgia and the South Sandwich Islands by reference to the Application of Colonies Laws 2012 No 2749 – The Liberia (Restrictive Measures) Ordinance 1967 (No 1of 1967, Falkland Islands). (Overseas Territories) (Amendment) Order 2012; 2. Section 5 of the Ordinance provides that the Police 2012 No 2750 – The Democratic Republic of the Congo Force shall consist of such police officers as may from time (Restrictive Measures) (Overseas Territories) (Amendment) to time be approved by the Commissioner and enrolled in Order 2012; the Force.
    [Show full text]
  • Research Vessel POLARSTERN PS119: 13.04
    Research vessel POLARSTERN PS119: 13.04. – 31.05.2019 Punta Arenas ‐ Port Stanley Sixth weekly report: 13. – 19. May, 2019 To the smoking volcano of Saunders Island Like last week, we spent the sixth week in the southernmost area of the South Sandwich Plate, from the back‐arc spreading ridge of the segments 8 and 9 in the west to the Kemp Caldera. The volcano of Kemp Caldera is part of the collision zone with the South American plate to the East. A look to our expedition logo shows symbolically the spreading ridge on the left and flowing to the right the volcanoes, fore‐arc area and subduction zone. The weather conditions, which denied from Sunday to Tuesday morning further dives, permitted not until Tuesday to dive down with ROV QUEST to the seafloor. We used the dive‐free time for the deployment of other sampling gear. On Sunday, 12th of May, we sampled the deepest area of the Kemp caldera with a 3 m long gravity corer and the multi‐corer. The until then surveyed Parasound profiles over the caldera showed in the deepest area narrow sediment layers, whose mineral and chemical composition in references to hydrothermal deposits are of huge interest. With our corers we were able to sample sediment layers of 230 cm depth, which surprised us by their colouring and diverse sediment compositions. Figure 1: Penguins being washed up by a wave’s high to an Figure 2: Analyses of sediment cores in the laboratory of an iceberg following by a steep climb (© Carsten Zillgen). Polarstern.
    [Show full text]