The elevated water table (EWT) technique for preventing acid mine drainage (AMD) was tested using instrumented laboratory columns containing reactive tailings from the Louvicourt and Sigma mines, Abitibi, Quebec. The tests were performed in short (0.4 m) and long (1.4-1.7 m) columns over 400-500 days and included periodic surface recharge and subsequent monitoring of the leached drainage water. In each column, the water table depth was adjusted relative to the air entry value (AEV or ψa) of the tailings. The influence of different water table elevations was evaluated by measuring the effluent pH, as well as the concentrations of major ions including sulphate, iron, zinc, copper and lead. Provided the water table depth below the tailings surface remained less than one half of the tailings' AEV, the observed data showed that an EWT can be very effective in reducing acid mine drainage. The principal factors controlling drainage quality were the saturated hydraulic conductivity (k sat) and the air entry value (ψa) of the tailings. A lower k sat and a higher ψa in the tailings tend to increase the performance of an elevated water table by limiting drainage-induced desaturation. Mineralogical composition had relatively little effect on the hydrogeochemical evolution provided the tailings remained highly saturated (S r ≥ 90%). The results presented here indicate that an elevated water table can be an effective means for controlling the production of AMD when the design conditions are properly selected and applied.

An ozone forecasting system has been developed based on the CALGRID photochemical dispersion model. The system is implemented as an experimental operational web service at the LaMMA Consortium to forecast ozone pollution over Tuscany region, Italy. It takes advantage of two daily forecasts, one reproducing the meteorology over Tuscany and the other providing chemical boundary conditions. Meteorological forecasts are performed by the Weather Research and Forecasting Nonhydrostatic Mesoscale Model (WRF-NMM) mesoscale model, which is operative at LaMMA for the daily forecasting service. Calculated at a 10-km resolution, WRF-NMM outputs are downscaled to the 4-km system's final resolution through the CALMET diagnostic model. Daily boundary conditions are forecast by the CHIMERE dispersion model of the PREV'AIR European air quality forecasting system. Since CHIMERE uses the MELCHIOR chemical mechanism, a suitable species conversion was required to the SAPRC-90 mechanism implemented in CALGRID. Emission data are provided by the Regional Inventory of the Sources of Emissions of the Tuscan Regional Authority. Each day, a 96-h simulation is run starting from 00 UTC of the preceding day, used to merely initialize the system, resulting in a 3-day forecast of ozone from today issued to the web in terms of ozone daily mean and maximum concentrations over Tuscany. The system was experimentally run over May to September 2007, resulting in a good accuracy compared to station observations.

This study aimed at determining the water quality of River Sirimon and River Kongoni, Ewaso Ng'iro North Basin, Kenya. Water quality analysis of these two rivers was done for a period of 5 months between November 2005 and February 2006. Portable Palintest equipment was used for the chemical analysis. The study established that there were sulphates concentrations of 22 mgL⁻¹ in the Kongoni River water associated with the use of commercial fertilisers as compared to mean values of 7 mgL⁻¹ along Sirimon River; phosphate concentrations were 1.3 mgL⁻¹ in Kongoni and 0.15 mgL⁻¹ in Sirimon and salinity 3 mgL⁻¹ in Kongoni and 0.47 mgL⁻¹ in Sirimon. On average, mean nitrates concentrations of 1.7 mgL⁻¹ were recorded for Kongoni River, which were higher than those recorded for Sirimon River (0.033 mgL⁻¹). These concentration levels were however within the standard levels set by WHO for example 50 mgL⁻¹ for nitrates (WHO 2008). River Kongoni has two major irrigated horticultural farms across it which were likely polluting the river during the time of this study.

In this work, the determination of moving averages is proposed as a method for quantifying metal, arsenic, and sulfate discharges into a water course undergoing acid mine drainage processes which flows into a public water supply dam in the Iberian Pyrite Belt. The analysis of the results obtained by applying moving averages shows that the highest metal and sulfate concentrations occur in October, coinciding with the first rainfall and the sponging of mine dumps, with November and December being the months when the highest contributions to the Andevalo Dam take place. The discharge of acid mine waters with its corresponding metal load into the Andevalo Dam means, for a single hydrological year, more than 6,000 t of sulfates, almost 600 t of iron, and 1 t of As, of special relevance for the hydrochemical quality of the stored waters. When they arrive at the dam, these metals precipitate, since the water pH is near 7, and remain latent in the bottom sediment as long as the chemical makeup of the dam water does not change.

This study is aimed at assessing the ability of metal-resistant yeast, Candida tropicalis, to uptake cadmium from the liquid medium. The minimum inhibitory concentration of Cd²⁺ against C. tropicalis was 2,800 mg L⁻¹. The yeast also showed tolerance towards Zn²⁺ (3,100 mg L⁻¹), Ni²⁺ (3,000 mg L⁻¹), Hg²⁺ (2,400 mg L⁻¹), Cu²⁺ (2,300 mg L⁻¹), Cr⁶⁺ (2,000 mg L⁻¹), and Pb²⁺ (1,200 mg L⁻¹). The yeast isolate showed typical growth curves, but low specific rate of growth was observed in the presence of cadmium. The yeast isolate showed optimum growth at 30°C and pH 7. The metal processing ability of the isolate was determined in a medium containing 100 mg L⁻¹ of Cd²⁺. C. tropicalis could decline Cd²⁺ 57%, 69%, and 80% from the medium after 48, 96, and 144 h, respectively. C. tropicalis was also able to remove Cd²⁺ 56% and 73% from the wastewater after 6 and 12 days, respectively. Cd produced an increase in glutathione (GSH) and non-protein thiol levels by 146.15% and 59.67% at 100 mg L⁻¹ concentration, respectively. Metal tolerance and accumulation together with changes in the GSH status and non-protein thiols under Cd exposure were studied in C. tropicalis.

Water hardness is well known to affect the toxicity of some metals; however, reports on the influence of hardness during incubation or acclimation on later toxicity to metals have been conflicting. We incubated rainbow trout (Oncorhynchus mykiss) near the confluence of two streams, one with soft water and one with very-soft water (average incubation hardnesses of about 21 and 11 mg/L as CaCO₃, respectively). After developing to the swim-up stage, the fish were exposed for 96-h to a mixture of cadmium (Cd) and zinc (Zn) in water with a hardness of 27 mg/L as CaCO₃. The fish incubated in the higher hardness water were about two times more resistant than the fish incubated in the extremely soft water. This difference was similar or greater than the difference that would have been predicted by criteria hardness equations had the fish been tested in the different acclimation waters. We think it is plausible that the energy demands for fish to maintain homeostasis in the lower hardness water make the fish more sensitive to metals that inhibit ionoregulation such as Cd and Zn. We suggest that if important decisions were to be based upon test results, assumptions of adequate hardness acclimation should be carefully considered and short acclimation periods avoided. If practical, incubating rainbow trout in the control waters to be tested may reduce uncertainties in the possible influences of differing rearing water hardness on the test results.

A study on pH and chemical composition of precipitation was carried out in two Italian sites, one urban (site 1) and one rural (site 2), located approximately 30 km far from Bologna, during a 3-year period. No significative site variation was found. In both locations, bulk deposition pH ranged from slightly acid to slightly alkaline, despite the volume weighted mean concentration of acidic species, NO ₃ ⁻ and SO ₄ ²⁻ (67.4 and 118.4 μeq l⁻¹ in site 1 and 88.7 and 103.8 μeq l⁻¹ in site 2), that were similar to those of typical acidic rainfall region. This might be ascribed to the neutralization reaction of the Ca²⁺, attributed to the calcareous soil and the frequent dusty air mass intrusion from the Sahara. The pair correlation matrix and the analysis of the main components suggested also ammonium and other crustal elements as neutralization agents. The depositional rate of SO ₄ ²⁻ and NO ₃ ⁻ , chemical elements of agricultural interest, amounted to 38 and 28 and 32 and 35 kg ha⁻¹ for site 1 and site 2, respectively. These supplies of nutrient were not negligible and had to be considered on cultivated lands. NH ₄ ⁺ deposition rate on site 2 was 7 kg ha⁻¹, 23% over site 1, probably due to nitrogen fertilization in the fields around the monitoring station. In site 1, SO ₄ ²⁻ presented a seasonal trend, indicating that its principal source was the residential heating. Results emphasized that the entity of the bulk deposition acidification is linked not only to the ions local emission sources (fossil fuel combustions, heating, and fertilizers) but also to the surrounding territory and the prevalent wind that transports through kilometers air masses which may contain acidic and alkaline species.

Atmospheric and sea sediment concentrations were measured for eight nitrated polycyclic aromatic hydrocarbons (nitro-PAHs) and three unsubstituted PAHs in a suburban area and sea sediments in the Hiroshima Bay watershed area, Japan, from July to December, 2006 (atmospheric particulate matter) and in September and November, 2004 (sea sediments). Atmospheric concentration was higher in winter than summer for both nitro-PAHs and PAHs. Concentrations in sea sediments were less than 10%, and pattern was similar to those of atmospheric particles. Several combustion emission sources were also measured, and the 1-NP/Pyr ratio was compared to environmental values. The ratio of atmospheric and sea sediments were significantly lower than diesel particulate matters. Further, the vehicle emission loading and sea sedimentation loading was evaluated in this watershed area, and from the comparison, the existence of other important sources PAHs were suggested.

The aim of the present study was to determine the influence of light soil fertilization using sewage sludges or composts on soil toxicity for three plant species (Lepidium sativum, Sorgo saccharatum, and Sinapis alba) and crustaceans (Heterocypris incongruens). The results obtained were compared to the polycyclic aromatic hydrocarbon (PAHs) content as a potential toxicity factor. The PAH content in soils fertilized with sludges was proportional to the dose applied. Soil fertilization with the studied materials negatively influenced plant growth and development. The negative influence was clearer in the case of sewage sludges than composts. Both sludges and composts significantly influenced H. incongruens mortality. However, the influence of sludges and composts on H. incongruens growth did not exceed 20%. The EC50 and LC50 values calculated on the basis of toxicity parameters showed that H. incongruens was characterized by a higher sensitivity to sludges and composts than most of the plants. L. sativum was characterized by the lowest EC50 values among all plants. No significant relationships between sewage sludge or compost toxicity and their PAHs content were observed.

The main objective of this study was to compare the effectiveness of different methods (heavy metals in pore water (PW), diffusive gradients in thin films (DGT), diethylene triamine pentaacetic acid (DTPA) extraction, and total heavy metals (THM) in soil) for the assessment of heavy metal bioavailability from soils having various properties and heavy metal contents. The effect of soil heavy metal pollution on shoot yield and sulfatase enzyme activity was also studied. Wheat (Triticum aestivum) was grown in different soils from Spain (n = 10) and New Zealand (n = 20) in a constant environment room for 25 days. The bioavailabilities of Cd, Cr, Cu, Ni, Pb, and Zn were assessed by comparing the metal contents extracted by the different methods with those found in the roots. The most widely applicable method was DGT, as satisfactory Cu, Ni, Pb, and Zn root concentrations were obtained, and it was able to distinguish between low and high Cr values. The analysis of the metal concentrations in PW was effective for the determination of Cr, Ni, and Zn content in root. Copper and Pb root concentrations were satisfactorily assessed by DTPA extraction, but the method was less successful with determining the Ni and Cr contents and suitable just to distinguish between high and low concentrations of Zn. The THM in soil method satisfactorily predicted Cu and Pb root concentrations but could only be used to distinguish between low and high Cr and Zn values. The Cd root concentration was not successfully predicted for any of the used methods. Neither shoot yield nor sulfatase enzyme activity was affected by the metal concentrations.