[Departement_IRSTEA]EEE [Departement_IRSTEA]GMA [TR1_IRSTEA]11 - VERSEAU / TRANSPOL | This program is part of the common research action AQUAE (2000-2003) between Cemagref and INRA. It aims at understanding and quantifying the mechanisms of retention, degradation and transport of pesticides at the field and the catchment scales. The study relates in particular to man-made impact causing hydrological discontinuities such as ditches network and grass and wooded cover zones. Experiments were undertaken on two catchments with different geomorphological and climatic characteristics, La Jaillière (44) and Roujan (34), in order to analyse the contamination of water by pesticides. The factors determining the efficiency of these man-made hydrological discontinuities are extensively studied : hydrometeorological conditions, geomorphological position, soil characteristics; land-use, vegetation cover classes, and the oxydo-reduction conditions. A typology of these various types of discontinuities is established on a great range of catchments, in order to characterise the various experimental situations and to ensure the applicability of the results on un-gauged catchments. Finally, a distributed hydrological modelling approach (the model MHYDAS : Modélisation Hydrologique Distribuée des AgroSystèmes = Distributed Hydrological Modelling of AgroSystems) of water and pollutant transfer, integrating the principal mechanisms observed on hydrological discontinuities in farmed catchments, is conceived and is in an advanced phase of development. The first tests of the model at the catchment scale enable the simulation of hydrograph and pesticides concentrations at various locations of ditches network. Furthermore, it enables the testing of various scenarios of land management and the impact of man-made planning on water and pesticides fluxes. | Ce programme fait partie de l'action structurante AQUAE (2000-2003) entre le Cemagref et l'INRA et a pour objectif de comprendre et quantifier les phénomènes de rétention, de dégradation ou de transfert subis par les produits phytosanitaires entre la parcelle agricole et le milieu aquatique. L'étude porte notamment sur les discontinuités hydrologiques que constituent les fossés et les dispositifs enherbés ou boisés. Ces structures font l'objet de suivis en continu et d'expériences spécifiques, afin d'analyser le devenir des produits phytosanitaires en leur sein, sur deux bassins versants aux caractéristiques différentes : La Jaillière (44) et Roujan (34). Les facteurs déterminant leur efficacité tampon sont étudiés, qu'il s'agisse des conditions hydrométéorologiques, de leurs positions géomorphologiques, des caractéristiques du sol ou de la végétation, et de l'alternance des conditions d'oxydo-réduction. Une typologie de ces différents types de discontinuités est établie sur une grande gamme de bassins versants sur lesquels les équipes participantes travaillent ou ont déjà travaillé. Cette typologie a permis de caractériser les principales situations existantes ou envisageables, afin d'assurer (la généralisation ou l'extrapolation) des résultats obtenus sur les bassins versants expérimentaux. Enfin, une approche de modélisation hydrologique distribuée (le modèle MHYDAS : Modélisation Hydrologique Distribuée des AgroSystèmes) des transferts d'eau et de polluants à l'échelle du versant, intégrant les principaux mécanismes observés sur les discontinuités hydrologiques, est en phase avancée de développement. Les premiers tests du modèle ont permis de simuler les hydrogrammes de crue en différents points du réseau de fossés et les ordres de grandeur des flux de pesticides à l'exutoire du bassin versant.

Small- and medium-scale mining operations in Guyana have increased significantly since the late 1980s. The majority of these gold mining operations utilize mercury (Hg) amalgamation methods in the recovery process, raising the question as to the significance of Hg inputs to the environment from mining activities. In March and April, 2001, 168 samples were collected from floodplain, sand bar, and channel bed deposits along a 350 km reach of the Mazaruni River and a 160 km reach of the Essequibo River. Distinct trends in the geochemical data suggest that much of the Hg found in the alluvial deposits is related to anthropogenic sources, including (1) Hg concentrations in floodplain, channel bed and sand bar deposits locally exceed background values defined by ferralitic soils; (2) core data reveal that Hg concentrations within floodplain deposits have increased in recent years; and (3) high Hg concentrations along the channels can be attributed to the influx of material from tributaries affected by mining operations, or to mining activities along the rivers. Recent investigations in Amazonia have argued that Hg from amalgamation mining represents a small portion of the total Hg load to riverine systems, the majority coming from the erosion of Hg enriched upland soils within deforested terrain. Geochemical data from the Essequibo and Mazaruni Rivers suggest that Hg from mining may be a more significant source in Guyana where large-scale deforestation is limited. However, it is unclear whether the increased Hg represents the direct input associated with the amalgamation process, or Hg associated with the erosion of soils and sediments that results from activities that accompany mining.

In Zacatecas, Mexico, four plants are operating to extract Ag, Au, and Hg using CaS₂O₃solution from surface soil containing tailings from the amalgamation method used during 1550–1900. The metal ions extracted are cemented by scrap Cu wires. Hg is separated by evaporation from the cemented amalgam and Ag and Au are obtained from the residue. A part of the soil to be leached was separated and leached as in the industrial process. Only 121 ppm of Hg was freed from 168 ppm of extractable Hg. About a half of the remaining Hg in the soil evaporated during 18 months. This confirms that the Hg in the soil is metallic. Pb and As are also freed in the same process. It is estimated that 13 000–34 000 t of Hg had been discarded in the extraction of Ag.

The hydrochemistry of mountain lakes is highly conditioned by the chemicalcomposition of atmospheric deposition and by climate characteristics. Consequently these ecosystems have proved to be sensitive to long-term changes in both factors. Climate warming seems to be particularly pronounced in the Alpine region. A reduction of snow cover in space and time, due to less precipitation and higher temperatures, means a greater exposure of rocks and soils in the watersheds, which enhances weathering processes. In this paper we aim to evaluate the possible effect of these processes on long-term changes in the chemistry of alpine lakes. Recent climate changes affecting the study area were investigated through a data series referring to temperature, precipitation, snow depth and duration at some stations in the Ossola Valley. Chemical data of 35 lakes located in the Ossola and Sesia Valleys (Central Alps) were used. Lakes were sampled both in the late summer of 2000 and 2001 in the framework of two European Projects and the results compared with previous data (1984–1987). Two lakes (Boden Superiore and Inferiore, 2343 and 2334 m a.s.l., respectively), located in the northern part of the study area, have been sampled more or less continuously since the late 70s, enabling us to evaluate the trends of the main chemical variables. For lakes lying in catchments with highly soluble rocks, a comparison between the two data sets shows an increase of solute contents in the last few years. This result could be attributed to increased weathering rates due to climate warming.

Research works on the removal of mercury from water by zeolitic mineralshow that small quantities of this element are sorbed. In this work the mercury sorption from aqueous solutions in the presence and absence of Cu(II), Ni(II) and Zn(II) onto a Mexican zeolitic mineral unmodified and modified with cysteamine hydrochloride or cystamine dihydrochloride was investigated in acidic pH. The zeolitic minerals were characterized by thermogravimetric analysis, scanning electron microscopy, X-ray diffraction and FTIR. The sorption kinetics behavior and the retention isotherms for mercury were determined in the natural and treated zeolitic mineral samples. It was found that the amounts of sulfur on the modified zeolitic minerals were 0.375 (cysteamine hydrochloride) and 0.475 (cystamine dihydrochloride) mmol g⁻¹, which were not saturated to their total capacities of adsorption for the maximum concentration used (0.310 mM). Under the experimental conditions, the retention of mercury was the highest for the zeolitic minerals treated with the organic compounds, with adsorption capacities ranging from 0.0107 to 0.0509 mmol Hg g⁻¹.The retention was not affected by the presence of others heavy metals studied in this work as expected.

Urban transportation activities generate a wide gradation of anthropogenic solids with varying physical and chemical properties. These solids accumulatein urban highway snow and remain as residual deposition material after the melting and recession of the snow from the pavement shoulder. This study analyzed the physical characteristics of these residuals and the associatedheavy metals for 10 urban highway sites located throughout metropolitan Cincinnati. Results from the residuals analyses indicate that for all sites particle gradations ranged from greater than 5000-μm to less than 25-μm with a mean d₅₀of 1225-μm. Specific gravity (ρₛg) of residual solids ranged from 2.5 to 3.2 as evaluated for intervals across thegradations, with the lower specific gravity associated with particles less than 100-μm. For each gradation, specific surface area (SSA) generally increased with decreasing particle size while the predominance of total surface area (SA) was associated with the coarser size fractions. Cumulativeanalysis for Pb, Cu, Cd and Zn associated with snow residuals indicated that more than 50% of the heavy metal mass was associated with particles greaterthan 250-μm and more than 80% was associated with particles greater than 50-μm. Results provide guidance for management of urban snow residuals and design of treatment strategies focused on these residuals.

In this study, the adsorption of phosphate on gas concrete from aqueous solutions has been studied as functions of temperature, mixing rates and suspension pH. Over 99% of phosphate removal was found. The chemical composition of the gas concrete has been defined by X-ray analysis. Experimental data was fitted to the Langmuir equation in order to Langmuir coefficients. After calculating Langmuir coefficients, adsorption free energy (Δ G⁰ₐdₛ.) has been determined. In order to gather information about adsorption mechanism, electrophoretic mobilites of particles were measured at various pHs by using Zeta meter 3.0+. It has been found that the adsorption is driven by the interactions between the ionizations of CaO and Al₂O₃and the formation of AlPO₄. According to the BET (N₂) measurements, the specific surface area of gas concrete was found as 22 m²g⁻¹. The surface area after adsorption has been found as 17 m²g⁻¹. The surface area covered by adsorbate has been found as 5.23 m²g⁻¹by usingaₛ= nˢₘ. aₘ. NA. These two areas determined by BET and Langmuir model were close to each other (BET: 22 m²g⁻¹–17 m²g⁻¹).

This paper is devoted to the assessment of the impact of the Upper Silesian Industrial Region on greenhouse gases emissions in Poland. Detailed analysis will cover emissions of methane and carbon dioxide which are characteristic for the mining and power engineering industry prevailing in this region. The industries of Silesia emit 16.2% of CO₂, and about 30% of methane emissions in Poland come from coal seams. The leading strategy to counteract this situation, not only in Upper Silesia, should involve the improved efficiency of energy use and decreased use of primary energy carriers.

We studied the environmental effects of the mining activity of Troya Mine on the fluvial ecosystem, in the Basque Country, Spain, from 1993 to 1995. The multivariate analysis of the physicochemical conditions shows that the main abiotic factors of variation are: (i) in the water column, a significant increase in the content of heavy metals and conductivity, and (ii) an intense accumulation of heavy metals in the bottom sediments. We studied the effects of these factors on density, richness, dominance, similarity coefficient and composition of the benthic macroinvertebrate community (BMI).We observed a de-structuring of the community. Richness decreases (from 25 to 11 different number of families), but it does not suitably value the impact. Density oscillates radically (255–1548 individuals m⁻²) and reflects changes occurred in sediments. Dominance, which oscillates from 0 to 1, increase from 0.16 upstream from the mine, to 0.42 downstream, fundamentally due to oscillations of Chironomidae, Tubificidae, Baetidae and Simuliidae. The similarity coefficient indicates the physicochemical variations both in the sediment and in the water column; this index is therefore suitable for the follow-up of the evolution of the disturbance studied. The families sensitive to disturbance in the water column are: Ephemeridae, Athericidae, Sericostomatidae, Leptophlebiidae, Baetidae, Gammaridae, Perlidae, Heptageniidae, and Leptoceridae; the tolerant ones are: Coenagrionidae, Hydrobiidae, Lumbricidae, and Polycentropodidae.With regard to the metal content in sediments, the sensitive families are: Gammaridae, Ephemeridae and Ceratopogonidae; the tolerant ones are: Simuliidae, Culicidae, Hydrophilidae, Dolichopodidae, Chironomidae, Psychodidae, Tipulidae, and Chrysomelidae.We thus synthesized the complexity inherent to this type of pollution, in which large amounts of variables are normally involved.

Bleached Kraft mill effluent was treated in an activated sludgereactor followed by an allophanic soil adsorption system (ASAS). Under aerobic conditions, removal efficiencies of biological oxygen demand (BOD₅) and chemical oxygen demand (COD) varied between 57.7–96.5% and 30.3–57.0%, respectively, depending on the hydraulic retention time (HRT). On the other hand, tannin-lignin and phenolic compounds removal efficiencies attained values between 13.2–51.2 and 3.6–33.5%,respectively. An allophanic soil adsorption system was designed for color and phenolic compounds removal. Three different types of soils were used: Natural allophanic soil as the control compared, with calcinated and acidified allophanic soil. The initial removal efficiencies for phenolic compounds varied between 72 an 87% for activated soils, while color initial removal efficiencies were between 95 and 99%. Moreover, COD and tannin-lignin initial removal efficiencies reached maximum values of 74 and 87%, respectively, for calcinated soil. Design parameters show that there is an enhancement factor in adsorption capacities for both activated soils. In fact, phenolic compounds breakpoint adsorption capacity increased 5.3 times for calcinated soil and 17.6 times for acidified soil, while saturation capacity increased between 2.2 and 3.2 times. In addition, color breakpoint adsorption capacity increased 2.8 times for calcinated soil and 10.4 times for acidified soil, while saturation capacity increased between 3.2 and 5.5 times.