Anne Hélène Fostier

Mercury fluxes in a natural forested Amazonian catchment (Serra do Navio, Amapá State, Brazil).

Mercury (Hg total) fluxes were calculated for rainwater, throughfall and stream water in a small catchment located in the northeastern region of the Brazilian Amazon (Serra do Navio, Amapá State), whose upper part is covered by a natural rainforest and lower part was altered due to deforestation and activities related to manganese mining. The catchment area is 200 km from the nearest gold mining (garimpo). Minimum and maximum Hg concentrations were measured monthly from October 1996 to September 1997 and were 3.5-23.4 ng l(-1) for rainwater, 16.5-82.7 ng l(-1) for throughfall (March-August 1997) and 1.2-6.1 and 4.2-18.8 ng l(-1) for stream water, in natural and disturbed areas, respectively. In the natural area, the inputs were 18.2 microg m 2 year(-1) in rainwater and 72 microg m(-2) year(-1) in throughfall. This enrichment was attributed to dry deposition. The stream output of 2.9 microg m(-2) year(-1) indicates that Hg is being recycled within the forest as other chemical species or is being retained by the soil system, as confirmed by the cumulative Hg burden in the 0-10 cm surface layer, which was 36480 microg m(-2). When the disturbed area of the catchment was included, the stream output was 9.3 microg m(-2), clearly indicating the impact of the deforestation of the lower part of the basin on the release of mercury. The Hg burden in the disturbed area was 7560 microg m(-2) for the 0-10 cm surface layer.

Arsenic removal from water employing heterogeneous photocatalysis with TiO2 immobilized in PET bottles.

Arsenic oxidation (As(III) to As(V)) and As(V) removal from water were assessed by using TiO2 immobilized in PET (polyethylene terephthalate) bottles in the presence of natural sunlight and iron salts. The effect of many parameters was sequentially studied: TiO2 concentration of the coating solution, Fe(II) concentration, pH, solar irradiation time; dissolved organic carbon concentration. The final conditions (TiO2 concentration of the coating solution: 10%; Fe(II): 7.0 mg l(-1); solar exposure time: 120 min) were applied to natural water samples spiked with 500 microg l(-1) As(III) in order to verify the influence of natural water matrix. After treatment, As(III) and total As concentrations were lower than the limit of quantitation (2 microg l(-1)) of the voltammetric method used, showing a removal over 99%, and giving evidence that As(III) was effectively oxidized to As(V). The results obtained demonstrated that TiO2 can be easily immobilized on a PET surface in order to perform As(III) oxidation in water and that this TiO2 immobilization, combined with coprecipitation of arsenic on Fe(III) hydroxides(oxides) could be an efficient way for inorganic arsenic removal from groundwaters.

Direct Determimnation of Mercury in Sediments by Atomic Absorption Spectrometry

A pyrolysis chamber is described for the direct determination of mercury in sediments by atomic absorption spectrometry. The finely ground and dried sample is weighed (2.0–60.0 mg), transferred to a quartz cup, inserted in a pyrolysis chamber and heated at 1100 °C for 30 s by means of three focused infrared lamps in the presence of an air stream as the carrier gas. Interfering substances are destroyed by a precolumn containing alumina, silica and copper(II) oxide, and the released mercury is amalgamated on to a gold-coated collector. Mercury vapour is later measured by AAS after thermal desorption. Calibration is easily performed by flow injection, in which known volumes of mercury-saturated air are introduced into the same air carrier stream. The absolute detection limit was 0.26 ng Hg and the relative standard deviation of measurements (n=12) from a typical 4.0 mg sample was about 7%. By applying a t-test, there was no significant difference at the 5% probability level between the results obtained with the proposed method and those certified or recommended for NIST materials. One analysis takes only 2 min, including sample weighing.

Sorption of norfloxacin in soils: analytical method, kinetics and Freundlich isotherms.

Fluoroquinolones are potent antibacterial agents that are active against a wide range of pathogenic organisms and are widely used in veterinary medicine. Fluoroquinolones and their metabolites may reach the soil through animal excreta or manure and may contaminate water and soils. The degree of sorption of these antimicrobials to soils varies widely, as does the mobility of these drugs. In the present study, sorption of norfloxacin in four soils of the state of São Paulo was investigated with batch equilibrium experiments. A strong matrix effect on the chromatographic determination of norfloxacin was verified. Sorption kinetics were best fit by a pseudo second-order model (r>0.99), and sorption/desorption isotherms were well fit by the Freundlich model in log form (r>0.97). Norfloxacin showed high affinity for soil particles, with KF sorption values ranging from 643 to 2410 μg(1-1/n)(cm(3))(1/n)g(-1) and KF desorption values ranging from 686 to 2468 μg(1-1/n)(cm(3))(1/n)g(-1). The high desorption KF values indicate that norfloxacin is highly immobile in the evaluated soils.

Major aspects of the mercury cycle in the Negro River Basin, Amazon

Despite the low level of industrial activity and human density, Hg concentration in the Negro River basin is relatively high. Soil enriched with naturally high Hg concentrations and atmospheric deposition are the main sources of the metal in this watershed. Differences between invasive and evasive fluxes at the water/air and soil/air interfaces indicate Hg accumulation in the basin at a rate of 39.9 t y-1. The type of soil, which is the main source of mercury for the water bodies, the hydrological cycle with floods and dry periods, act markedly on the water redox chemistry. A complex interaction between many seasonable variables such as solar intensity, water pH, age of the naturally occurring organic matter and the hydrological cycle alter the redox characteristics of these black water bodies, thus markedly affecting the consumption of Hg0 and the degradation of methylmercury present in the water. Although methylation is favored in black waters, photodegradation counterpoints this formation, thus regulating the methylmercury burden in the water column.

Preliminary results of mercury levels in raw and cooked seafood and their public health impact

Mercury is toxic for human health and one of the main routes of exposure is through consumption of contaminated fish and shellfish. The objective of this work was to assess the possible mercury contamination of bivalves (Anomalocardia brasiliana, Lucina pectinata, Callinectes sapidus), crustacean (C. sapidus) and fish (Bagre marinus and Diapterus rhombeus) collected on Salinas da Margarida, BA (Brazil), a region which carciniculture, fishing and shellfish extraction are the most important economic activities. The effect of cooking on Hg concentration in the samples was also studied. The results showed that Hg concentration was generally higher in the cooked samples than in raw samples. This increase can be related to the effect of Hg pre-concentration, formation of complexes involving mercury species and sulfhydryl groups present in tissues and/or loss of water and fat. The highest concentrations were found in B. marinus samples ranging 837.0-1585.3 μg kg(-1), which exceeded those recommended by Brazilian Health Surveillance Agency (ANVISA). In addition, Hg values found in the other samples also suggest the monitoring of the Hg concentrations in seafood consumed from the region.

Assessment of Direct Mercury Analyzer ® to Quantify Mercury in Soils and Leaf Samples

This work aims to assess a method for total Hg quantification in soil and leaf samples by using a Direct Mercury Analyzer® (DMA-80 TRICELL; Milestone Inc., Italy). Standard Reference materials of tree leaves, river sediment and soil, and collected samples of soil and leaves were used to optimize and to validate the method. Given that the technique allows direct analysis of samples by combustion, aspects like effect of sample amount variation and sample granulometry were considered. Methods robustness was also assessed through the Youden test showing that for leaf sample analyses, among the seven tested factors, four were able to significantly affect the analytical results, but the soil samples results were not significantly affected by slight variations of any of the seven factors. Recoveries for reference materials ranged from 102% to 104%, and the precision (RSD) was lower than 5%.

Gaseous and particulate atmospheric mercury concentrations in the Campinas Metropolitan Region (São Paulo State, Brazil)

The concentrations of Total Gaseous Mercury (TGM) and Total Particulate Mercury (TPM) were monitored during the 2002-2003 rainy and dry seasons at two sampling points (industrial and residential areas) of the Campinas Metropolitan Region. No significant difference was observed between the concentrations found at the two sampling areas and the mean values were 7.0 ± 5.8 ng m-3 (TGM) and 0.4 ± 0.3 ng m-3 (TPM). The analysis of the diel variability showed higher TGM concentrations during the day, which could be related to more intense anthropogenic activity during the day. Atmospheric dispersion processes could also explain some seasonal variation observed in TGM concentrations. For TPM concentrations a decreasing trend was observed during the rainy season, which could be explained by the removal of particles by wet deposition. The concentrations of TGM and TPM found in this study were of the same order of magnitude of those recorded in some highly industrialized regions of the northern hemisphere. These data show that emissions from the most industrialized Brazilian regions, and probably from similar regions in other countries of the southern hemisphere, should also be assessed and integrated into the global anthropogenic mercury emission assessment.

Ocorrência, comportamento e impactos ambientais provocados pela presença de antimicrobianos veterinários em solos

Antimicrobials, among other veterinary drugs, are used worldwide in industry and agriculture to protect animal health and prevent economic loss. In recent years, they have been detected in various environmental compartments, including soil, surface and groundwater and have become a topic of research interest. Emphasizing this class of compounds, this review presents the different pathways which veterinary drugs enter in the environment, in particular contaminate soils. Also are presented regulatory aspects and guidelines, adsorption/desorption and degradation of these compounds in soils and the consequences of its dispersal in the environment.

Quantificação de fluxos de mercúrio gasoso na interface solo/atmosfera utilizando câmara de fluxo dinâmica: aplicação na bacia do Rio Negro

Gaseous mercury sampling conditions were optimized and a dynamic flux chamber was used to measure the air/surface exchange of mercury in some areas of the Negro river basin with different vegetal coverings. At the two forest sites (flooding and non-flooding), low mercury fluxes were observed: maximum of 3 pmol m-2 h-1 - day and minimum of -1 pmol m-2 h-1 - night. At the deforested site, the mercury fluxes were higher and always positive: maximum of 26 pmol m-2 h-1 - day and 17 pmol m-2 h-1 - night. Our results showed that deforestation could be responsible for significantly increasing soil Hg emissions, mainly because of the high soil temperatures reached at deforested sites.