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Interactions of nonylphenol (NP), a toxic and oestrogenic degradation product of widely used non-ionic surfactants, with the cyanobacterium Microcystis aeruginosa were studied. Batch cultures were incubated for 10 days with NP concentrations between 10 and 570 nM. NP was removed more quickly in the presence of M. aeruginosa (half-life 2.7-5.2 days) than in its absence (half-life 6.7-10.2 days) at all concentrations tested. At the end of the experiment, NP could not be found in the biomass, so the biotic removal is due to uptake and chemical transformation, and not to physical binding on the cells. The observed effective concentrations, EC50 and EC20, were 0.45 and 0.25 μ M, respectively. Therefore, NP is expected to have toxic effects on M. aeruginosa only in very contaminated surface waters. However, for concentrations that go far beyond environmental levels, cyanobacteria are able to cope with NP toxicity by internalising the compound in a less toxic form. Therefore, the presence of cyanobacteria may increase the rate of NP removal from the aquatic environment. [ABSTRACT FROM AUTHOR]

In spite of a worldwide reduction in the utilization of organochlorine pesticides (OCPs), they are still a problem for the aquatic environment and human health. The Black Sea is still being polluted with persistent chemicals, including OCPs. Aquatic organisms (sprat, scad, bluefish, shad, belted bonito, goby, and black mussel) with different feeding behaviours were sampled on a seasonal basis from the Bulgarian region of the Black Sea, and the concentrations of 13 OCP residues were determined. Although many of the OCPs were not detected in the samples, in all samples 1,1,1-trichloro-2,2-bis(4-chlorophenyl) ethane (DDT) was present mainly in the form of its metabolites 1,1-dichloro-2,2-bis(4-chlorophenyl) ethane (DDD) and 1,1-dichloro-2,2-bis(4-chlorophenyl) ethylene (DDE). Only about 12% of the total DDT was present as the parent compound pp-DDT, which suggests that it was not being used recently in the region. The total DDT concentrations were generally below 150 μg kg-1 fresh weight, but higher levels - up to 354 μg kg-1 fresh weight - were also measured for fish species with a high fat content. Between-species differences were observed, even when the concentrations were presented on a fat-level basis. DDT concentrations did not show any significant changes over the 2-yr sampling period. Fish sampled in the northern areas of the Bulgarian Black Sea coast seemed to contain higher DDT levels than those from the southern areas, suggesting a major (historical) influence of the Danube River. For permanent monitoring purposes, the utility of Black Sea gobies and scad should be considered. [ABSTRACT FROM AUTHOR]

Surface waters were collected in the River Adour estuary (south-western France) during different sampling periods from 1998 to 2001 in order to investigate the phase distribution and speciation of methylmercury (MeHg + ). Although a high variability is observed, significant higher average concentrations of total MeHg + (dissolved and particulate) are measured during the warm seasons, at 4.40±8.18 pM and 3.90±1.87 pM for July 1998 and September 1999, compared with the winter seasons, with concentrations at 0.99±2.85 pM and 1.00±1.75 pM for February 1998 and February 2001, respectively (one-tailed t -test, P =0.01). The seasonal variations are explained with enhanced bacterial activity during summer and sedimentation/resuspension phenomena. Additionally, signi-ficant longitudinal variations of the MeHg + concentrations are observed. The highest levels in both dissolved and particulate fractions are found within the downstream urban estuarine area. This can be explained by the high methylation potential of the sediments, but direct anthropogenic inputs of MeHg + from specific discharge points cannot be neglected. Biogeochemical factors like phytoplankton biomass and salinity also show a relationship with MeHg + partitioning in the surface waters of the Adour estuary. [ABSTRACT FROM AUTHOR]

A modified automated on-line hyphenated system for simultaneous inorganic ionic mercury (Hg2+) and monomethylmercury (MeHg+) analysis by hydride generation (HG) or ethylation (Eth), cryofocussing, gas chromatography (GC) separation and atomic fluorescence spectrometry (AFS) detection has been improved. Both derivatization methods are investigated with respect to the chromatographic and analytical performances. They can be both affected by interferences when the AFS detection system is used. Water vapor removal using a soda lime moisture trap improves significantly the chromatographic performances, the reproducibility and the detection limits for Hg2+ and MeHg+ analyzed with both methods. For ethylation (Eth) derivatization, a scattering interference generated from low-quality ethylation reagent has also been eliminated. For HG, improved detection limits are 0.13 ng l−1 and 0.01 ng l−1 for Hg2+ and MeHg+, respectively (0.1 l water sample), and reproducibility are 5% for Hg2+ (20 ng l−1) and MeHg+ (5 ng l−1). Improved detection limits for Eth are 0.22 ng g−1 for Hg2+ and 0.02 ng g−1 for MeHg+ (1 g dry sediment sample) and the reproducibility are 5–6% for Hg2+ and MeHg+ (1–2 ng g−1). [Copyright &y& Elsevier]