Comparative study of potential transfer of natural and anthropogenic cadmium to plankton communities in the North-West African upwelling.

A Lagrangian approach based on a physical-biogeochemical modeling was used to compare the potential transfer of cadmium (Cd) from natural and anthropogenic sources to plankton communities (Cd-uptake) in the North-West African upwelling. In this region, coastal upwelling was estimated to be the main natural source of Cd while the most significant anthropogenic source for marine ecosystem is provided by phosphate industry. In our model experiment, Cd-uptake (natural or anthropogenic) in the North-West African upwelling is the result of an interplay between the Cd dispersion (by advection processes) and the simulated biological productivity. In the Moroccan waters, advection processes limit the residence time of water masses resulting in a low natural Cd-uptake by plankton communities while anthropogenic Cd-uptake is high. As expected, the situation is reversed in the Senegalo-Mauritanian upwelling where natural Cd-uptake is higher than anthropogenic Cd-uptake. Based upon an estimate of Cd sources, our modeling study shows, unexpectedly, that the anthropogenic signal of potential Cd-bioaccumulation in the Moroccan upwelling is of the same order of magnitude as the natural signal mainly present in the Senegalo-Mauritanian upwelling region. A comparison with observed Cd levels in mollusk and fishes, which shows overall agreement with our simulations, is confirming our estimates.

Determination of ultra-trace Sb(III) in seawater by stripping chronopotentiometry (SCP) with a mercury film electrode in the presence of copper.

This work reports the determination of ultra-trace of Sb(III) in seawater by using a stripping chronopotentiometric (SCP) method with a mercury film electrode. A sensitivity and detection limit of 360 ms L microg(-1) and 8 ng L(-1) (70 pM), respectively, were accomplished for a 15-min electrolysis time. Compared to the only two chronopotentiometric methods reported for Sb(III) determination in seawater, our method is more sensitive and does not need to use a medium exchange procedure before the stripping step. Moreover, the use of a double electrolysis potential (-450 mV and -250 mV) allows the analysis of Sb(III) independently from the Cu level in the sample. The method was successfully used to study the behaviour of dissolved Sb(III) in the Penzé estuary, NW France.