DOCSLIB.ORG

Biomarqueurs Lipidiques, Réseau Trophique Pélagique Et Écologie Alimentaire Des Oiseaux De Mer Procellariiformes

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Biomarqueurs Lipidiques, Réseau Trophique Pélagique Et Écologie Alimentaire Des Oiseaux De Mer Procellariiformes Thèse de doctorat de l’Université Pierre et Marie Curie - Paris VI Spécialité : Océanologie Biologique Ecole Doctorale : Sciences de l’Environnement d’Ile de France Présentée par Maëlle Connan En vue d’obtenir le grade de Docteur de l’Université Paris VI BBiioommaarrqquueeuurrss lliippiiddiiqquueess,, rréésseeaauu ttrroopphhiiqquuee ppééllaaggiiqquuee eett ééccoollooggiiee aalliimmeennttaaiirree ddeess ooiisseeaauuxx ddee mmeerr PPrroocceellllaarriiiiffoorrmmeess Soutenu le 9 décembre 2005, devant le jury composé de : M. G. Bourdier Professeur, Université Blaise Pascal Rapporteur M. P. Jouventin Directeur de recherche, CNRS Rapporteur M. P. Nival Professeur, Université Paris VI Examinateur M. G. Duhamel Professeur, MNHN Examinateur M. P. Mayzaud Directeur de recherche, CNRS Directeur de thèse M. Y. Cherel Directeur de recherche, CNRS Co-directeur de thèse Remerciements Je tiens vivement à remercier celles et ceux qui m’ont soutenu au cours de ces trois dernières années et qui ont rendu ce travail possible : Je tiens tout d’abord à exprimer ma profonde reconnaissance à mes deux directeurs de thèse, Messieurs Patrick Mayzaud et Yves Cherel, qui m’ont accordé leur confiance et dont la complémentarité a beaucoup enrichie ce travail. Merci pour votre disponibilité et vos conseils avisés. Je remercie sincèrement Messieurs Gilles Bourdier et Pierre Jouventin qui m’ont fait l’honneur d’être rapporteurs de cette thèse. Je tiens à remercier chaleureusement Messieurs Paul Nival et Guy Duhamel d’avoir accepté de juger ce travail. Toute ma gratitude s’adresse à M. Louis Legendre, Directeur du Laboratoire d’Océanographie de Villefranche, pour m’avoir accueillie au sein du laboratoire mais surtout pour son soutien tant financier que scientifique lors de ma participation à la Gordon Conférence sur les milieux polaires. Je suis également très reconnaissante envers Mme Christiane Lancelot pour son soutien lors de cette même conférence. Je remercie l’ensemble des membres de l’équipe ‘Réponses biologiques et physiologiques aux contraintes du milieu’ qui m’ont permis de réaliser ce travail dans les meilleures conditions. Mes remerciements s’adressent également à M. Patrick Duncan, Directeur du Centre d’Etudes Biologiques de Chizé, pour ses discussions fructueuses sur le régime alimentaire des herbivores… Voici le résultat… Merci d’avoir rendu possible mes séjours à Chizé, lieu d’échanges passionnants tant scientifiques qu’humains. Merci à Henri Weimerskirch, Directeur de l’équipe ‘Prédateurs marins’, pour l’échantillonnage en Tasmanie réalisé avec Yves Cherel. Je tiens à remercier M. Guy Duhamel d’avoir accepté de céder quelques spécimens de poissons ; ces analyses ont grandement amélioré le travail de thèse. Je remercie chaleureusement Marc Boutoute, spécialiste es lipides, Colette Trouvé, spécialiste es tris de contenus stomacaux, Stéphanie Sabini, spécialiste es Mac Gyver. Merci pour vos compétences, votre aide, votre soutien et surtout votre bonne humeur. Sans vous j’y serai encore… Les prélèvements de cette thèse ont été effectués par de nombreux volontaires à l’aide technique aussi bien à Kerguelen qu’à Crozet. J. Martin, G. Mabille, F. Bailleul et F. Pawlowski, P. Bocher, B. Labidoire, F. Jiguet, G. Fradet, O. Duriez, G. Juin, S. Caulle, D. Secondi, D. Pinaud, J. Spaggiari, S. Chamaillé, C. Vanpé, O. Villa, N. Delelis, V. Chartendrault, C. Marteau et J.L. Chil, sans vous cette thèse n’aurait pas vu le jour… Merci d’avoir bravé les éléments pour récupérer des contenus stomacaux d’oiseaux… Je tiens à remercier Raffaella Cattaneo, Yannig Coulomb et Anne-Flore Thailly pour leurs aides dans l’analyse des échantillons de prions de Belcher et de pétrels à menton blanc. Je remercie particulièrement Nicolas Gasco, Olivier Duriez, Tony Palliser et Steve Johnson dont les photographies peuplent ce manuscrit. Mon travail dans les deux laboratoires n’aurait pu aboutir sans l’efficacité de plusieurs personnes que souhaite remercier chaleureusement : Michèle Etienne, Isabelle Courtois, Martine Fiorini au LOV, Evelyse Rouby, Dominique Besson au CEBC, Alain Nierga et Laurence Touchon à l’Université Paris VI. Un certain nombre de collaborations m’ont permis d’enrichir mes connaissances et d’ouvrir d’autres horizons : Pierrick Bocher (merci pour les données, l’article devrait bientôt être écrit…), Marie Nevoux (merci pour les informations de démographie, et pour l’intérêt que tu portes à ce travail), Peter Nichols, Charles Phleger, Matthew Nelson, Katrina Phillips (merci pour ces échanges de données lipidiques), Hugh Dove (merci d’avoir montré de l’intérêt à ce travail si éloigné du vôtre), Eric Woehler (merci de m’avoir apporté un nouveau regard sur mon travail et pour les discussions si intéressantes). Je tiens à remercier très sincèrement Catherine Thiriot pour les nombreuses relectures de ce manuscrit, des articles, et surtout pour ce soutien de tous les instants… Pardon d’avoir occupé tes matinées avec mes données d’oiseaux et de lipides… Je suis sûre que tu es devenue une vraie pro ! J’ai également une pensée pour tous les amis et collègues que j’ai croisés tant à Villefranche qu’à Chizé au cours des différents séjours que j’ai effectués dans les deux stations. Un grand MERCI à Osana et Martin, ce n’est que le début d’une belle amitié… petite dédicace à Eve et Céline, bonnes fées de la Vieille Forge… Enfin, je tiens à remercier ma famille et particulièrement ma grand-mère Jacqueline, mon père Yannick, et ma sœur Solène (merci pour ces relectures… et conseils statistiques), merci de votre présence et de votre soutien… A ma mère… Merci… TABLE DES MATIERES Table des Matières ......................................................................................................................... i Liste des Abréviations.................................................................................................................... v Liste des Figures ............................................................................................................................ vi Liste des Tableaux ......................................................................................................................... viii INTRODUCTION GENERALE............................................................................1 CHAPITRE I : CONTEXTE SCIENTIFIQUE, PRESENTATION DES MATERIELS ET METHODES A. Contexte scientifique ....................................................................................................6 1. Les prédateurs supérieurs marins..................................................................................... 6 1.1. Pourquoi étudier les prédateurs supérieurs ?..................................................................... 6 1.2. Cas des oiseaux marins de l’Océan Austral ...................................................................... 7 2. Etude des relations prédateurs-proies.............................................................................. 7 2.1. Définition.......................................................................................................................... 7 2.2. Méthodes d’étude.............................................................................................................. 8 2.2.1. Méthodes d’analyse des contenus stomacaux ................................................................... 8 2.2.2. Méthodes des traceurs alimentaires................................................................................... 9 3. Les lipides marqueurs trophiques..................................................................................... 11 3.1. Définition.......................................................................................................................... 11 3.2. Base de la chaîne alimentaire............................................................................................ 13 3.3. Maillons supérieurs........................................................................................................... 14 4. Les huiles stomacales chez les Procellariiformes............................................................. 15 4.1. Formation des huiles stomacales....................................................................................... 15 4.2. Rôles des huiles stomacales .............................................................................................. 17 4.3. Etudes antérieures sur les huiles stomacales..................................................................... 18 B. Cadre géographique et modèles d’étude ....................................................................20 1. L’Océan Austral................................................................................................................ 20 2. Les sites d'étude ................................................................................................................ 22 2.1. Ile Bruny ........................................................................................................................... 22 2.2. Archipel de Crozet ............................................................................................................ 23 2.3. Archipel de Kerguelen ...................................................................................................... 24 3. Les Procellariiformes........................................................................................................ 25 3.1. Le puffin à bec grêle ......................................................................................................... 27
Load more

Recommended publications
  • 788 RR MAKAROV & AI DANILOV (Eds.)
    788 R. R. MAKAROV& A. I. DANILOV(eds.), Investigations of the Weddell Gyre. Oceanographic conditions and peculiarities of the development of plankton communities: 140-160 [in Rus- sian]. (VNIRO Publication, Moscow). MAKAROV,R. R. & L. L. MENSHENINA,1992. Larvae of euphausiids off Queen Maud Land. Polar Biology, 11: 515-523. MAKAROV,R. R., L. L. MENSHENINA& V. I. LATOGURSKY,1993. Fishery of Antarctic krill (Euphausia superba Dana) and problems of rational exploitation of its resources. Antarctica, 32: 111-124 [in Russian]. MAKAROV,R. R. & V. A. SPIRIDONOV,1993. Life cycle and distribution of Antarctic krill. Some results of studies and problems. In: N. M. VORONINA(ed.), Pelagic ecosystems of the Southern Ocean: 158-168 [in Russian]. (Nauka, Moscow). BATHMANN,U. V., R. R. MAKAROV,V. A. SPIRIDONOV& G. ROHARDT,1993. Winter distribution and overwintering strategies of the Antarctic copepod species Calanoides acutus, Rhincalanus gigas and Calanus propinquus (Crustacea, Calanoida) in the Weddell Sea. Polar Biology, 13: 333-346. APPLICATION OF ULTRASOUND TECHNOLOGY TO CRUSTACEAN PHYSIOLOGY; MONITORING CARDIAC AND SCAPHOGNATHITE RATES IN BRACHYURA BY PAUL A. HAEFNER, JR. Rochester Institute of Technology, Department of Biology, Rochester, New York 14623, U.S.A. Machines used in diagnostic radiology and cardiology have application to crus- tacean organ systems. Gribble & Reynolds (1993), and Gribble (1994) demon- strated the use of angiography to describe cardiovascular function in a crab. In January 1994, I made preliminary ultrasound scans of a live crayfish. Although sagittal and transverse series of images produced little resolution of internal or- gans, movements of the heart and scaphognathites were easily detected. This paper reveals the ability to monitor the activities of these organs in brachyuran crabs.
    [Show full text]
  • Fatty Acid and Alcohol Composition of the Small Polar Copepods, Oithona and Oncaea : Indication on Feeding Modes
    Polar Biol (2003) 26: 666–671 DOI 10.1007/s00300-003-0540-x ORIGINAL PAPER G. Kattner Æ C. Albers Æ M. Graeve S. B. Schnack-Schiel Fatty acid and alcohol composition of the small polar copepods, Oithona and Oncaea : indication on feeding modes Received: 2 April 2003 / Accepted: 28 July 2003 / Published online: 27 August 2003 Ó Springer-Verlag 2003 Abstract The fatty acid and alcohol compositions of the (Paffenho¨ fer 1993). They occur from the polar seas to Antarctic copepods Oithona similis, Oncaea curvata, tropical regions at both hemispheres. Species of both Oncaea antarctica and the Arctic Oncaea borealis were genera can reach high concentrations, exceeding 5,000 determined to provide the first data on their lipid bio- individuals m)3 (Dagg et al. 1980; Koga 1986; chemistry and to expand the present knowledge on their Paffenho¨ fer 1993; Metz 1996). The high abundance of feeding modes and life-cycle strategies. All these tiny these tiny species compensates for the low biomass and, species contained high amounts of wax esters (on average thus, the populations can reach biomass levels of the 51.4–86.3% of total lipid), except females of Oithona same order as dominant calanoid species (Metz 1996). In similis (15.2%). The fatty-acid composition was clearly the Southern Ocean, Oithonidae and Oncaeidae can dominated by 18:1(n-9), especially in the wax-ester-rich account for between 20 and 24% of the total copepod Oncaea curvata (79.7% of total fatty acids). In all species, biomass (Schnack-Schiel et al. 1998). 16:0 and the polyunsaturated fatty acids 20:5(n-3) and The epipelagic species, Oithona similis, has been de- 22:6(n-3), which are structural components of all mem- scribed as the most numerous and widely distributed branes, occurred in significant proportions.
    [Show full text]
  • Advances in MARINE BIOLOGY
    Advances in MARINE BIOLOGY VOLUME 46 ThisPageIntentionallyLeftBlank Advances in MARINE BIOLOGY Edited by A. J. SOUTHWARD Marine Biological Association, The Laboratory, Citadel Hill, Plymouth, PL1 2PB, UK P. A. TYLER School of Ocean and Earth Science, University of Southampton, Southampton Oceanography Centre, European Way, Southampton, SO14 3ZH, UK C. M. YOUNG Oregon Institute of Marine Biology, University of Oregon P.O. Box 5389, Charleston, Oregon 97420, USA and L. A. FUIMAN Marine Science Institute, University of Texas at Austin, 750 Channel View Drive, Port Aransas, Texas 78373, USA Amsterdam – Boston – Heidelberg – London – New York – Oxford Paris – San Diego – San Francisco – Singapore – Sydney – Tokyo This book is printed on acid-free paper. ß 2003 Elsevier Science Ltd. All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the Publisher. The appearance of the code at the bottom of the first page of a chapter in this book indicates the Publisher’s consent that copies of the chapter may be made for personal or internal use of specific clients. This consent is given on the condition, however, that the copier pay the stated per copy fee through the Copyright Clearance Center, Inc. (222 Rosewood Drive, Danvers, Massachusetts 01923), for copying beyond that permitted by Sections 107 or 108 of the U.S. Copyright Law. This consent does not extend to other kinds of copying, such as copying for general distribution, for advertising or promotional purposes, for creating new collective works, or for resale.
    [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]
  • Calanoides Acutus and Calan Us Propinquus
    I MARINE ECOLOGY PROGRESS SERIES Vol. 97: 135-142.1993 Published July l5 ' Mar. Ecol. Prog. Ser. 1 Calanoides acutus and Calanus propinquus, Antarctic copepods with different lipid storage modes via wax esters or triacylglycerols Wilhelm ~agen',Gerhard Kattner2,Martin ~raeve~l 'Institut fir Polarokologie, Universitlt Kiel, WischhofstraBe 1-3, Geblude 12, D-24148 Kiel, Germany Z~lfred-Wegener-~nstitutfiir Polar- und Meeresforschung, Am Handelshafen 12, D-27570 Bremerhaven. Germany ABSTRACT: The dominant large copepods Calanoides acutus and Calanus propinquus were collected south of 65's in the Antarctic Weddell Sea in late winter-early spring (October-November) and summer (January-February), and the lipid and fatty acid/alcohol compositions of copepodite stages V and females of these suspension feeders were analyzed. The lipids of C. acutus consisted mainly of wax esters. Major fatty acids in summer were 20:l(n-g), 20:5(n-3), 22:6(n-3), 18:4(n-3), 22:l(n- 11) and 16:l(n-7). In winter the amount of 18:4(n-3) decreased considerably in both stages, as did that of 20:5(n-3) in females, whereas the quantity of 20:l(n-9) showed a strong increase in females. During both seasons the fatty alcohols in the wax esters were strongly dominated by 20:l(n-9) and 22:1 (n- 11). In contrast, the bulk of the llpids of C. proplnquus were tnacylglycerols with the principal fatty acids 22:l(n- ll),22:l(n-g), 16:0, 20:5(n-3) and 22:6(n-3).
    [Show full text]
  • Observations of Neutral Buoyancy in Diapausing Copepods Calanoides Acutus During Antarctic Winter
    Polar Biol DOI 10.1007/s00300-014-1525-7 SHORT NOTE Observations of neutral buoyancy in diapausing copepods Calanoides acutus during Antarctic winter Sabine Schru¨nder • Sigrid B. Schnack-Schiel • Holger Auel • Franz Josef Sartoris Received: 23 January 2014 / Revised: 27 May 2014 / Accepted: 28 May 2014 Ó Springer-Verlag Berlin Heidelberg 2014 Abstract The herbivorous Antarctic copepod Calanoides Keywords Zooplankton Á Copepod Á Calanoides acutus Á acutus overwinters inactively in a resting stage (diapause) Antarctic Á Diapause Á Buoyancy Á Ammonium at depths below 500 m. It is assumed that during diapause C. acutus is neutrally buoyant in order to retain energy reserves otherwise depleted by swimming activities. Introduction However, so far, no experimental observations on its buoyancy have been reported and our knowledge of The two dominant Antarctic copepod species, Calanoides buoyancy regulation mechanisms is incomplete. In the acutus and Calanus propinquus, have developed opposing present study, species-specific differences in buoyancy life-cycle strategies in order to survive periods of food were assessed visually. Observations were made of speci- scarcity in austral winter. They show distinct seasonal, mens from the diapausing cohort of C. acutus and com- inter-specific, and stage-dependent differences in behavior, pared to another herbivorous copepod Calanus propinquus, physiological condition, and biochemical composition. C. which overwinters actively feeding in the upper water acutus descends to depths below 500 m and survives the layers. Freshly caught copepods were anaesthetized in a food-limited winter season by remaining inactive during a 3-amino-benzoic acid ethyl ester (MS222) in seawater resting stage (diapause) for several months.
    [Show full text]
  • Calanus Propinquus and Calanoides Acutus in the Weddell Sea
    Polar Biol 32001) 24: 771±784 DOI 10.1007/s003000100283 ORIGINAL PAPER Anna F. Pasternak á Sigrid B. Schnack-Schiel Seasonal feeding patterns of the dominant Antarctic copepods Calanus propinquus and Calanoides acutus in the Weddell Sea Accepted: 13 April 2001 / Published online: 26 June 2001 Ó Springer-Verlag 2001 Abstract The diets and feeding activity patterns of two rigid in Calanoides acutus, and more ¯exible in Calanus dominant Antarctic copepods, Calanus propinquus and propinquus. Calanoides acutus, were studied throughout the seasonal cycle on material from several ``Polarstern'' cruises to the southeastern Weddell Sea. The observed dierences in feeding patterns were closely linked with the pecu- Introduction liarities of the life-cycle strategies and changed with ambient food concentration. Calanoides acutus under- The feeding patterns of the dominant Antarctic plank- went diapause at depth and was never found feeding in ton copepods are closely linked with their life-cycle winter. The winter descent of the population of Calanus strategies 3Atkinson 1998; Pasternak and Schnack- propinquus was less pronounced, as some of the older Schiel, in press). The two most extensively studied large copepodids stayed in the upper layer and contained copepods, Calanoides acutus and Calanus propinquus, food. The period of active feeding in Calanoides acutus follow basically the same strategy and possess similar was shorter than in Calanus propinquus. The former did foraging features. However, even these closely related not start feeding before late in spring. Feeding activity at species dier in patterns of seasonal 3ontogenetic) ver- the main study region 3south of 67°S) was compared tical migrations 3Voronina 1970; Voronina et al.
    [Show full text]
  • Regional Differences in the Life Cycle of Calanoides Acutus (Copepoda: Calanoida) Within the Atlantic Sector of the Southern Ocean
    MARINE ECOLOGY PROGRESS SERIES Vol. 150: 99-111, 1997 Published April 30 Mar Ecol Prog Ser I Regional differences in the life cycle of Calanoides acutus (Copepoda: Calanoida) within the Atlantic sector of the Southern Ocean A. ~tkinson'~',S. B. ~chnack-Schie12,P. Ward', V. ~arin~ 'British Antarctic Survey, Natural Environment Research Council, High Cross, Madingley Road, Cambridge CB3 OET, United Kingdom Z~lfred-Wegener-Institutfiir Polar- und Meeresforschung, Columbusstrasse, D-27568 Bremerhaven, Germany "niversidad de Chile, Fac. Ciencias, Depto. CS Ecologicas. Casilla 653, Santiago, Chile ABSTRACT: All suitable data from the Atlantic sector of the Southern Ocean were compiled to eluci- date regional differences in the abundance and life cscle of Calanoides acutus. Data from 205 stations (1928 to 1992) were pooled into 3 regions, namely thc Scotia Sea (SS),the Weddell-Scotia Confluence/ northern Weddell Sea area (WSC) and the Eastern Weddell Sea (EWS). The regions contrast sharply: the ice-free SS has summer mixed layer temperatures -3 to 4°C higher but summer chlorophyll a con- centrations generally lower than the EWS, which is ice-covered for three-quarters of the year C. acu- tuswas rarer in the vicinity of the WSC than in the southern part of the SS or In the EM'S. In all 3 regions seasonal vertical migration characterised the populations, but their appearance in the surface waters of the SS was 1 to 2 mo earlier than in the EWS, and was of longer duration. Because C. acutus is herbiv- orous, this is presumably a response to the timing of summer primary production.
    [Show full text]
  • Life Cycle Strategies of Epipelagic Copepods in the Southern Ocean
    Journal of Marine Systems 15Ž. 1998 289±311 Life cycle strategies of epipelagic copepods in the Southern Ocean Angus Atkinson ) British Antarctic SurÕey, Natural EnÕironment Research Council, High Cross, Madingley Road, Cambridge CB3OET, UK Revised 8 April 1997; accepted 26 September 1997 Abstract Twelve epipelagic copepod species were reviewed to compare their adaptations to the short primary production season and low temperatures which characterise the Southern Ocean. The species show a spectrum of adaptations, but three broad life cycle strategies were defined:Ž. 1 herbivorous in summer, a short reproductive period and winter diapause at depth Ž.Ž.Calanoides acutus and possibly Ctenocalanus citer ; 2 predominantly omnivorousrdetritivorous diet, an extended period of feeding, growth and reproduction and less reliance on diapause at depth Ž Metridia gerlachei, Calanus propinquus, Calanus simillimus, Oithona similis, Microcalanus pygmaeus, and possibly Oncaea curÕata and Oithona frigida.Ž.;3 overwintering and feeding within sea ice as early nauplii or copepodids Ž.Stephos longipes and Paralabidocera antarctica . The large species Rhincalanus gigas appears to be intermediate between strategiesŽ. 1 and Ž. 2 . Contrasting species from groupsŽ. 1 and Ž. 2 , namely C. acutus and O. similis, were selected for more detailed comparison. For C. acutus, maximum Ž.probably food saturated feeding and egg production rates are well below equivalent values for Calanus spp. at lower latitudes. Likewise, summer growth and moulting rates are slower, and the growth season of this herbivore is only 2±4 months. Therefore, both the low summer temperatures and short primary production season seem to dictate a long Ž.;1 year life cycle for C.
    [Show full text]
  • Lipid Storage in Marine Zooplankton
    MARINE ECOLOGY PROGRESS SERIES Vol. 307: 273–306, 2006 Published January 24 Mar Ecol Prog Ser REVIEW Lipid storage in marine zooplankton Richard F. Lee1,*, Wilhelm Hagen2, Gerhard Kattner3 1Skidaway Institute of Oceanography, 10 Ocean Science Circle, Savannah, Georgia 31406, USA 2Marine Zoologie, Universität Bremen (NW2), Postfach 330440, 28334 Bremen, Germany 3Alfred-Wegener-Institut für Polar- und Meeresforschung, Postfach 120161, 27515 Bremerhaven, Germany ABSTRACT: Zooplankton storage lipids play an important role during reproduction, food scarcity, ontogeny and diapause, as shown by studies in various oceanic regions. While triacylglycerols, the primary storage lipid of terrestrial animals, are found in almost all zooplankton species, wax esters are the dominant storage lipid in many deep-living and polar zooplankton taxa. Phospholipids and diacylglycerol ethers are the unique storage lipids used by polar euphausiids and pteropods, respec- tively. In zooplankton with large stores of wax esters, triacylglycerols are more rapidly turned over and used for short-term energy needs, while wax esters serve as long-term energy deposits. Zooplankton groups found in polar, westerlies, upwelling and coastal biomes are characterized by accumulation of large lipid stores. In contrast, zooplankton from the trades/tropical biomes is mainly composed of omnivorous species with only small lipid reserves. Diapausing copepods, which enter deep water after feeding on phytoplankton during spring/summer blooms or at the end of upwelling periods, are characterized by large oil sacs filled with wax esters. The thermal expansion and com- pressibility of wax esters may allow diapausing copepods and other deep-water zooplankton to be neutrally buoyant in cold deep waters, and they can thus avoid spending energy to remain at these depths.
    [Show full text]
  • Distributional Records of Ross Sea (Antarctica) Planktic
    ZooKeys 969: 1–22 (2020) A peer-reviewed open-access journal doi: 10.3897/zookeys.969.52334 DATA PAPER https://zookeys.pensoft.net Launched to accelerate biodiversity research Distributional records of Ross Sea (Antarctica) planktic Copepoda from bibliographic data and samples curated at the Italian National Antarctic Museum (MNA): checklist of species collected in the Ross Sea sector from 1987 to 1995 Guido Bonello1, Marco Grillo1, Matteo Cecchetto1,2, Marina Giallain2, Antonia Granata3, Letterio Guglielmo4, Luigi Pane2, Stefano Schiaparelli1,2 1 Italian National Antarctic Museum (MNA, Section of Genoa), University of Genoa, Genoa, Italy 2 Depart- ment of Earth, Environmental and Life Science (DISTAV), University of Genoa, Genoa, Italy 3 Department of Chemical, Biological, Pharmaceutical and Environmental Sciences (ChiBioFarAm), University of Messina, Messina, Italy 4 Stazione Zoologica Anton Dohrn (SZN), Villa Pace, Messina, Italy Corresponding author: Stefano Schiaparelli ([email protected]) Academic editor: Kai Horst George | Received 23 March 2020 | Accepted 9 July 2020 | Published 17 September 2020 http://zoobank.org/AE10EA51-998A-43D5-9F5B-62AE23B31C14 Citation: Bonello G, Grillo M, Cecchetto M, Giallain M, Granata A, Guglielmo L, Pane L, Schiaparelli S (2020) Distributional records of Ross Sea (Antarctica) planktic Copepoda from bibliographic data and samples curated at the Italian National Antarctic Museum (MNA): checklist of species collected in the Ross Sea sector from 1987 to 1995. ZooKeys 969: 1–22. https://doi.org/10.3897/zookeys.969.52334 Abstract Distributional data on planktic copepods (Crustacea, Copepoda) collected in the framework of the IIIrd, Vth, and Xth Expeditions of the Italian National Antarctic Program (PNRA) to the Ross Sea sector from 1987 to 1995 are here provided.
    [Show full text]
  • Temporal Changes in Abundances of Large Calanoid Copepods in the Scotia Sea
    1 Temporal changes in abundances of large calanoid copepods in the Scotia Sea: 2 comparing the 1930s with contemporary times. 3 4 Peter Ward, Geraint A. Tarling, Sally E. Thorpe 5 6 7 British Antarctic Survey (Natural Environment Research Council) 8 High Cross 9 Madingley Rd 10 Cambridge 11 CB3 0ET 12 UK 13 14 Corresponding author: [email protected] 15 16 ORCID 17 Peter Ward: https://orcid.org/0000-0001-8260-1077 18 Geraint Tarling: http://orcid.org/0000-0002-3753-5899 19 Sally Thorpe: http://orcid.org/0000-0002-5193-6955 20 21 1 22 Abstract 23 To investigate whether impacts of reported climate change in the Antarctic marine 24 environment has affected mesozooplankton populations, we compared the summertime 25 abundances of 4 species of large calanoid copepods from samples taken during the Discovery 26 Investigations (1926-1938) and contemporary times (1996-2013). Discovery samples were 27 obtained using an N70V closing net fished vertically through 3 depth horizons encompassing 28 the top 250 m of the water column, whereas contemporary samples were obtained using a 29 Bongo net fished vertically through 200-0 m. Data from a previous study comparing catch 30 efficiencies of the two nets were used to generate calibration factors which were applied to 31 the N70V abundances. Following further corrections for net depth differences and seasonal 32 biases in sampling frequency, three of the four species, Calanoides acutus, Rhincalanus gigas 33 and Calanus simillimus, were found to be between ~20-55% more abundant in contemporary 34 times than they were 70 years ago.
    [Show full text]