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tel-00009359, version 1 - 1 Jun 2005<br />

Chapitre 3 - Fonctionnement du réseau trophique benthique de la Grande Vasière<br />

For isotopic analysis, SPM and TPM were filtered on pre-combusted Whatman GF/F filters<br />

before storage at –20°C. Subsequently, the filters were exposed to HCl fume for 4 h in order to remove<br />

carbonates before being placed in tin cups. The samples were analysed for isotope ratios using a<br />

Finnigan Delta S isotope ratio mass spectrometer coupled to a Carlo Erba NA 2100 Element Analyzer<br />

to allow POC and PON measures. Stable isotope ratios were expressed in conventional δ notation as<br />

parts per mil (‰) according to the following equation:<br />

δ X = [ (R sample/R standard) – 1 ] x 1,000 (1)<br />

where X is 13 C or 15 N and R is the corresponding 13 C/ 12 C or 15 N/ 14 N ratio.<br />

Pigments were extracted in 90% acetone, chlorophyll a and phaeopigments were measured on<br />

a Turner 112 fluorometer according to Lorenzen (1967).<br />

Benthic macrofauna organisms were identified to species level for most taxonomic groups<br />

(except for nematods, nemerteans, phoronids and chelicerates), counted and weighed (ash-free dry<br />

weight) after burning at 450°C for 4 hours. Benthic macrofaunal biomasses were then displayed in<br />

three major trophic groups, i.e. suspension feeders, deposit feeders and carnivores, according to<br />

Fauchald and Jumars (1979) and Bonsdorff and Pearson (1999).<br />

In order to characterise the degree of water column stability, a stratification index (SI) based<br />

on the water volumic mass (σt) differences by 5-m water cross-sections (Bustillos-Guzman et al., 1995<br />

modified by Lampert et al., 2002) was computed, using the following equation:<br />

n<br />

∆σ<br />

∑<br />

i=<br />

1 ∆z<br />

SI =<br />

n<br />

t<br />

x 10 4<br />

where i = number of 5 m cross-sections in the water column and z = depth.<br />

Re-suspension estimate<br />

Re-suspension of bottom sediments may influence the sedimentation rates of particulate matter<br />

measured by traps in macrotidal environments. To estimate the amount of particles re-suspended and<br />

re-sedimented into the traps, three different methods were used. The first one was a ratio method<br />

taking the chemical composition of particulate matter in the water column, in the traps and in the<br />

sediment into account (Gasith, 1975; Tagushi, 1982; Clavier et al., 1995). The concentration of any<br />

chemical compound in the trapped material can be expressed as a function of its value in the sediment<br />

and in the suspended material:<br />

Ct = XCs + (1-X)Cr<br />

Where Ct, Cs and Cr are the percentages of the given element in trap, SPM and sediment,<br />

respectively and X is the proportion of sedimented material in the trap. In this study, percent organic<br />

carbon has been used to calculated X, following Bhaskar et al. (2000).<br />

179<br />

(2)<br />

(3)

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