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ABSTRACT We report here the first inventory of mercury (Hg) contamination in the ecosystem of Vientiane city, a representative emerging city bordering the Mekong River. Total Hg (THg) concentration in soil and sediments of both... more
ABSTRACT We report here the first inventory of mercury (Hg) contamination in the ecosystem of Vientiane city, a representative emerging city bordering the Mekong River. Total Hg (THg) concentration in soil and sediments of both contrasting non-urbanized (wetland, rice paddy, Mekong River) and urbanized areas (wastewater canal and associated wastewater irrigated wetland) were low (8 to 101 ng g- 1), reflecting the essentially non-industrialized status of the capital. Dissolved THg (2.2 ± 2.2 ng l- 1) and monomethyl-mercury (MMHg) concentrations (0.06 ± 0.09 ng l- 1) were also low in both surface and soil or sediment pore water with higher concentrations (up to 9 ng g- 1 THg and 0.53 ng g- 1 MMHg) measured in wetlands and rice paddies suboxic waters. Dissolved organic carbon was identified as the main carrier in surface water for dissolved Hg transport towards the Mekong River. The measurement of low THg concentrations in rice (6.4 ± 1.0 ng g- 1) and fish (51 ± 40 ng g- 1) sampled in rice paddies and in the Mekong River confirmed the pristine state of the ecosystem of Vientiane area. Based on these data, we evaluated a low environmental Hg-attributable health risk for the local population whose diet relies on both fish and rice.
Total mercury concentrations in French Guyana river sediments were determined near gold mining sites and compared to unaffected reference sites. In small meter-size rivers the anthropogenic impact is localized and characterised by high... more
Total mercury concentrations in French Guyana river sediments were determined near gold mining sites and compared to unaffected reference sites. In small meter-size rivers the anthropogenic impact is localized and characterised by high total mercury peak concentrations in the mg/kg dry weight range (St. Elie site). The mercury load is more diluted in larger water streams such as the Inini
ABSTRACT Bacterial cells and bacterial exopolysaccharides differ strongly in their respective colloidal and polymeric habits. This suggests different reactivities toward metals and protons, although recent studies point to the similarity... more
ABSTRACT Bacterial cells and bacterial exopolysaccharides differ strongly in their respective colloidal and polymeric habits. This suggests different reactivities toward metals and protons, although recent studies point to the similarity of such substrates in terms of site density and metal complexation strength. The aim of this paper is to investigate the causes of this surprising uniqueness by studying the reactivity of a model exopolysaccharide, xanthan. NMR and molecular analysis were used to unambiguously determine the total density of reactive carboxylic sites of the xanthan molecule (1.65mmol/g xanthan dry weight dw). This allowed the independent determination of the average protonation constant of xanthan (Xan), which is more acidic than its constitutive reactive ligands, glucuronic and pyruvic acids (Glc+Pyr) at high (0.5) and medium (0.1), but not at low (0.01) ionic strength. This shows that xanthan is intrinsically more acidic than its constitutive reactive ligands, and that electrostatic effects developed at low ionic strength can limit the relative lability of xanthan's protons. A cylindrical electrostatic model based on the molecular structure of xanthan identified a single intrinsic constant (pKI=0=1.95±0.1) as the only adjustable parameter needed to fit our experimental data. The density of xanthan reactive sites (1.65. mmol/g dw) is comparable to that of whole bacterial cells and with known highly reactive biopolymers such as humic substances, nucleic acids, proteins, and polysaccharides (~. 1 to 5. mmol/g dw). The surprising similarity in site densities of these substrates is explained by the constitutive reactive site versus carbon concentration ratio, which is 1/23 in xanthan (one out of 23 carbons bears an acid-base reactive functional group), which is about the same in bacteria, and which increases to 1/6 in fulvic acids. These high ratios suggest the physical limits of stability for these polymers, and thus their high and similar site densities.