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A study of the particulate organic carbon (POC) in the estuarine turbidity maxima (ETMs) of the three major French macrotidal estuaries shows that the average contents are 1.5, 3.3 and 3.1% (expressed in % of dry suspended sediment) in the Gironde, Loire and Seine Estuaries, respectively. There is no seasonal variation of POC contents in the Gironde Estuary, whereas, they often increase in the Loire and the Seine Estuaries in spring and summer. The lability of the estuarine particulate organic matter was estimated by two analyses: 1/labile organic matter was measured as the organic carbon loss during incubation tests over one month; 2/ the hydrolysable organic fraction was determined after 6N HCl digestion. The organic fractions of the ETMs are mainly refractory. Any increase in the amount of POC as compared to the background levels (cited above) is always correlated to an increase of organic matter lability. The yearly average fluvial contributions by various particulate organic pools (soil and litter organic matter; organic matter of phytoplanktonic and human origin) that enter the three estuaries were quantified. In the Garonne River, soil and litter are the major (90%) POC sources. In the Loire system, due to the eutrophication of the river water, phytoplankton contributes up to 50% of the total POC load. In the Seine river, soil and litter contribute 70% of the total POC input; POC of human origin is also significant (10%), due to the impact of the City of Paris (10 million inhabitants). The lability of the different types of organic matter ranks as follows: phytoplankton~litter > humanorigin organic matter > > soil. By combining the POC budgets and the lability of each type of organic fraction, it was possible to explain why the POC of the three ETMs is different and characterizes its refractory vs. labile nature.

Mathematical modelling was combined with experimental Cu isotope measurements to demonstrate the effect of the sample matrix in changing the absolute and relative abundances of spectral interferences from Ti and Cr species. This unforeseen non-spectral effect, evidenced by variable inaccuracies of the different Zn-normalised Cu isotope ratios, was investigated by comparing real sedimentary samples and artificial solutions intended to match the Cu:Ti:Cr ratios of the real samples after (one-or two-step) chromatographic processing. Artificial solutions showed positive bias in δ 65 Cu X/Y with the magnitude depending on (1) the 6X Zn/ 6YZn ratio used for normalisation, (2) the Ti/Cu ratio and (3) the transmission Accepted Article