CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
CONTENT - International Society of Zoological Sciences
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
ICZ2008 – Abstracts S20<br />
Fat reserves and moisture content in relation to sexual cycle<br />
<strong>of</strong> sardine, Sardina pilchardus (Walbaum., 1792), in the<br />
eastern middle adriatic fishery grounds<br />
Gorenka Sinovčić and Bosiljka Mustać<br />
Institute <strong>of</strong> oceanography and Fisheries, Split, Croatia<br />
The fat reserves, moisture and sexual cycle <strong>of</strong> sardine, Sardina<br />
pilchardus (Walbaum, 1792), were studied from monthly random<br />
samples <strong>of</strong> purse seine catches from March 2004 to February<br />
2005. Catches were realised in <strong>of</strong>fshore (Dugi Otok) and inshore<br />
waters (Virsko more) <strong>of</strong> the Mid Adriatic Sea. A total <strong>of</strong> 1,219<br />
sardine specimens were collected, out <strong>of</strong> which 668 were males<br />
and 541 females. Fish were measured, weighed and sexed. The<br />
sexual cycle analysis was based on the temporal evolution <strong>of</strong><br />
gonadosomatic index and gonad mass. Gonadosomatic index<br />
(GSI) was calculated by expressing the monthly gonad weight as a<br />
proportion <strong>of</strong> the total body weight. The fat content was examined<br />
on the basis <strong>of</strong> monthly analyses <strong>of</strong> mesenteric fat in the visceral<br />
cavity and by determining the amount <strong>of</strong> lipid content in sardine<br />
tissues using Soxhlet’s s method. The total length <strong>of</strong> sardine<br />
ranged from 13.0 to 19.0 cm and the mass ranged from 16.72 to<br />
51.45 g. The reproductive period was from October to May,<br />
coinciding with the highest gonad weights and gonadosomatic<br />
indices. The mean percentage <strong>of</strong> mesenteric fat grades in visceral<br />
cavity points to the greatest fat quantities in August, when grade 4<br />
(fattest fish) presence amounted to 72%. The value is the result <strong>of</strong><br />
an increase <strong>of</strong> mesenteric fat started in June and proceeding in the<br />
successive months until October. During autumn, a decrease trend<br />
is evident and it becomes pronounced in winter and spring when<br />
the lowest mesenteric fat quantities are recorded. Thereafter an<br />
increase in mesenteric fat for sardine was recorded, indicated by<br />
the records <strong>of</strong> grades 3 and 4. Due to such variations in<br />
mesenteric fat and tissue lipid during year, i.e. its greatest levels in<br />
summer (out <strong>of</strong> spawning) and lowest levels in the colder part <strong>of</strong><br />
the year (during sardine spawning), it was assumed that quantity<br />
<strong>of</strong> sardine fat was affected by its sexual cycle. Lipid content in<br />
terms <strong>of</strong> sardine tissue dry weight showed the same trends as<br />
mesenteric fat - highest amounts during resting phase <strong>of</strong><br />
reproduction (41.1%) and lowest during the peak <strong>of</strong> spawning (1.0-<br />
2.2%). Amounts <strong>of</strong> total lipids and moisture in sardine tissues<br />
showed that females had more fat content and less moisture than<br />
males. An inverse correlation between fat content and sexual<br />
cycle on one side and lipid content and moisture on the other has<br />
been noted.<br />
Nutritional strategies <strong>of</strong> Pectinodonta sp., a gastropod<br />
associated with sunken woods<br />
Magali Zbinden 1,2 , Marie Pailleret 1,2,3 , Juliette Ravaux 1,2 , Sébastien<br />
Halary 1,2 , Françoise Gaill 1,2 and Sébastien Duperron 1,2<br />
1 UPMC, Laboratoire Systématique Adaptation et Evolution, 7 Quai<br />
St Bernard, 75252 Paris, France;<br />
2 CNRS, UMR7138, Systématique, Adaptations, Evolution, AMEX,<br />
7 Quai St Bernard, 75252 Paris, France;<br />
3 CNRS UMR 5143 Paléodiversité et Paléoenvironnements,<br />
Laboratoire de Paléobotanique, UPMC, 12 rue Cuvier, 75005 Paris,<br />
France<br />
The occurrence <strong>of</strong> sunken wood and vegetal debris in deep<br />
oceanic environments has been known for a long time (Murray<br />
1895; Wolff 1979).<br />
Sunken woods are abundant in the deep sea, at all depths, with<br />
higher densities near estuaries, and in sedimentary accumulation<br />
basins. Wood reaches abyssal depths in sufficient quantity to<br />
support locally the development <strong>of</strong> long-lasting ecosystems,<br />
playing a key role in the deep sea (Cayré & Richer de Forges<br />
2002).<br />
The faunal diversity that colonize sunken woods is widespread,<br />
comprising gastropod, polyplacophoran and bivalve molluscs,<br />
decapod and peracarid crustaceans, polychaetes, and<br />
echinoderms (Turner 1973, 1977, Cayré & Richer de Forges 2002).<br />
Until now, the only well known organisms able to degrade wood<br />
(thanks to symbiotic association with cellulolytic bacteria) and to<br />
use it as a food source are wood boring mollusca (Teredinidae and<br />
Xylophagainae) and isopodes crustacea (Limnoridae) (Gareth<br />
Jones et al. 2001).<br />
- 85 -<br />
During several cruises dedicated to sample sunken woods around<br />
Vanuatu, some species were observed stuck in hollows that they<br />
seem to dig at the surface <strong>of</strong> dregded woods. The most numerous<br />
species observed is a true limpet (Patellogastropoda) <strong>of</strong> the genus<br />
Pectinodonta, the species being still undescribed.<br />
The present work combine various approaches (microscopic<br />
observations <strong>of</strong> the radula, gills, and gut content; molecular<br />
methods to determine occurrence, localisation and phylogenetic<br />
position <strong>of</strong> associated microorganisms, and enzymatic assays to<br />
look for cellulolytic activity) to determine wether wood is a food<br />
source for this species and what are the terms and conditions <strong>of</strong> its<br />
degradation.<br />
New insigths on the metabolic diversity among the epibiotic<br />
microbial communitiy <strong>of</strong> the hydrothermal shrimp Rimicaris<br />
exoculata<br />
Magali Zbinden 1 , Bruce Shillito 1 , Nadine Le Bris 2 , C. de Villardi de<br />
Montlaur 1 , E. Roussel 3 , F. Guyot 4 , Françoise Gaill 1 and Marie-<br />
Anne Cambon-Bonavita 3<br />
1<br />
UMR CNRS 7138, Systématique, Adaptations et Evolution,<br />
UPMC, 7 Quai Saint Bernard, 75252 Paris cedex 05, France:<br />
2<br />
Département Environnement Pr<strong>of</strong>ond, Ifremer DRO, BP 70,<br />
29280 Plouzané, France;<br />
3 Laboratory <strong>of</strong> Microbiology <strong>of</strong> Extreme Environments, Ifremer<br />
Brest, LM2E, UMR 6197, BP 70, 29280 Plouzané, France;<br />
4<br />
Institut de Physique du Globe de Paris, Laboratoire de<br />
Minéralogie-Cristallographie, Université Paris-Jussieu, Tour 16,<br />
Case 115, 4, place Jussieu, 75 252 Paris Cedex 05, France<br />
The shrimp Rimicaris exoculata (Williams and Rona, 1986)<br />
dominates the megafauna <strong>of</strong> some <strong>of</strong> the Mid Atlantic ridge<br />
hydrothermal vent sites. This species harbors a rich community <strong>of</strong><br />
bacterial epibionts inside its gill chamber. Literature data indicate<br />
that a single 16S rRNA phylotype dominates this epibiotic<br />
community, and is assumed to be a sulfide-oxidizing bacteria.<br />
However attempts <strong>of</strong> cultivation were not successful and did not<br />
allow to confirm it. The aim <strong>of</strong> our study was to test the hypothesis<br />
<strong>of</strong> sulfide oxidation in the gill chamber, by a multidisciplinary<br />
approach, using in vivo experiments at in situ pressure in the<br />
presence <strong>of</strong> sulfide, microscopic observations and a molecular<br />
survey. Morphology <strong>of</strong> microorganisms, before and after treatment,<br />
was analyzed to test the effect <strong>of</strong> sulfide depletion and re-exposure.<br />
Our observations, as well as molecular data indicate a wider<br />
diversity than previously described for this shrimp’s epibiotic<br />
community. We observed occurrence <strong>of</strong> bacterial intracellular<br />
sulfur- and iron-enriched granules and some methanotrophic-like<br />
bacteria cells for the first time. Genes that are characteristic <strong>of</strong><br />
methane-oxidizing (pmoA) and sulfide-oxidizing (APS) bacteria<br />
were identified. These results suggest that three metabolic types<br />
(iron, sulfide and methane oxidation) may co-occur within the<br />
epibiont community associated with Rimicaris exoculata. As this<br />
shrimp colonizes chemically contrasted environments, the relative<br />
abundance <strong>of</strong> each metabolic type could vary according to the<br />
local availability <strong>of</strong> reduced compounds.