To determine the importance of Al-availability for soil micro-organisms 95 forest soils from Tyrol/Austria with comparable topography, vegetation, climatic conditions, soil type and with low soil pH (median = 3.9) were investigated for their physical (percentage of stable aggregates, water holding capacity), chemical (pH, electrical conductivity, contents of organic matter, concentrations of easily extractable aluminium, calcium, potassium, magnesium and phosphorus) and microbiological characteristics (microbial biomass and respiration, metabolic quotient, content of ATP, activities of protease and CM-cellulase, cfu-values of total and Al-tolerant bacteria and fungi). A highly significant negative correlation was detected between concentrations of KCl-extractable aluminium and soil pH. By the application of multivariate statistical methods, the effect of the concentration of KCl-extractable aluminium on abundance and activities of soil micro-organisms could be revealed. Al turned out to be of great importance for micro-organisms and often outmatched the significance of other well known soil properties like organic matter, pH or water holding capacity. However, due to very healthy trees at the sites under investigation no effect of Al or soil acidification on forest decline could be detected.

Fomesafen, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide, is used widely for weed control in soybeans since its introduction to China. Little information is available on its adsorption, desorption and movement in Chinese soils. The adsorption, desorption and mobility of fomesafen in six Chinese soils was studied. Adsorption isotherms agreed with the Freundlich equation very well. The results of regressionanalysis indicated that soil pH was more important than organic matter for fomesafen adsorption. Fomesafen was more readily desorbed from soils with 0.01 M CaSO₄solution. Soil TLC and column leaching studies showed that fomesafen and its metabolites was less mobile in Chinese soils. About 89.82% of applied fomesafen and its metabolites still remained in upper 5 cm layer 60 days after treatment under field conditions.

A photochemical puff-trajectory model (Fotoplume) has been applied to simulate emissions, atmospheric transport and chemical transformations of pollutants from offshore oil and gas production in the North Sea. The above model was used in conjunction with the European Monitoring and Evaluation Programme (EMEP) regional Lagrangian oxidant model. The Fotoplume and EMEP models were used to evaluate the effects of the atmospheric emissions from the oil and gas exploration activity in the Norwegian sector of the North Sea. Deposition of nitrogen and formation of boundary level ozone in Southern Norway due to North Sea emissions of nitrogen oxides (NOₓ), carbon monoxide (CO) and volatile organic compounds (VOC) have been studied. The petroleum activity in the North Sea is calculated to contribute approximately 20% of the nitrogen deposition in the coastal areas of Norway in 1992. In addition, the models were used to estimate the AOT40 ozone exposure levels. The results indicate that emissions from British and Norwegian oil and gas exploitation sector separately contribute to less than 5% each of the AOT40 values for coniferous forests and meadows. Comparison of model calculations with experimental measurements is quite satisfactory and the models show realistic results for both the nitrogen deposition and AOT40 values.

In this study, local air quality impacts of a proposed conventionalcoal-fired power plant in the İçel region has been investigated using numerical dispersion modeling studies coupled with a GIS application. Within the impact area of the facility, Industrial Source Complex Short Term (ISCST2) dispersion model has been used to estimate ground-level concentrations of air pollutants originating from the power plant. For the same impact area, GIS applications have been utilised to determine the agricultural yield distribution. For this purpose, relevant satellite images were digitised, classified and statistically analyzed. Based on the predicted ground-level pollutant concentrations and sensitivity of the agricultural crops to the pollutants, agricultural yield loss was estimated for the impact area.The results have been quantified and valuated in monetary terms for the purpose of performing an environmental cost benefit analysis. Comparison of the conventional cost benefit analysis with the environmental cost benefit analysis showed the significance of the external cost of the proposed facility, resulting from the environmental damages.

Attempt has been made to study the treatability of printing ink wastewatergenerated from an Indian currency printing press using coagulation-flocculation process. Coagulant agents, viz. ferrous sulphate, ferric chloride, aluminium sulphate and polyaluminium chloride were studied to select the most suitablecoagulant for effective treatment, and attain the optimum coagulant concentration. Cationic polyeletrolyte in conjunction with the most effective coagulant was also studied to assess its effect on floc settleability. Polyaluminium chloride (PAC) was found to be the most efficient coagulant, achieving removals of colour, suspended solids (SS), biochemical oxygen demand (BOD) and chemical oxygen demand (COD) of 95.9–96.5%, 96.5–97.0%, 61.3–65.8%and 54.8–61.8%, respectively at an optimum concentration of 1500 mg L⁻¹. Other coagulants, viz. ferrous sulphate, ferric chloride and aluminium sulphate did not show substantial removals of colour, BOD and COD, except suspended solids in comparison to the performance of PAC. Cationic ploylectrolyte in combination with PAC at an optimum concentration of 1500 mg L⁻¹of PAC and 1.0 mg L⁻¹of polyelectrolyte further improved the removal efficiency of various parameters studied, in addition to improving the floc settling rate, and reduction in quantity of sludge generation.Effect of rapid mixing intensity expressed as mean temporal velocity gradient (G), and mixing time (t) on flocculation was also investigated. Rapid mixing at an impeller rotational speed (n) of 300 rpm and mixing time (t) of 60 sec indicated good floc formation, which resulted in achieving velocity gradient of 821 s⁻¹, and was found to be an optimum combination. This was also indicated by relatively high settling velocity of sludge formed and low residual colour in the supernatant. However, slow mixing beyond 5 min, adopted after initial optimum rapid mixing, indicated negligible effect on flocculation.

More than 600 arable soils from Flanders (Northern-Belgium) were analysed for their total acid extractable contents of As, B, Be, Cd, Co, Cr, Cu, Mn, Ni, Pb and Zn in order to determine any increase in the natural background values. Samples were taken at random in several municipalities throughout Flanders. Areas with known historical or actual sources of trace element emissions were omitted although in some cases the distance between those sources and the sampling locations was not more than 20 km. The main soil types were, ranging from north to south: sand, loamy sand, light sandy-loam, sandy-loam and loam. In the coastal area, clay soils (sea polders) were sampled. In addition to the analysis of trace elements, the soil texture class, the pH and the carbon content were determined. Macro- or mesonutrients, Ca, K, P, Mg and Na, were determined from a weak acid extract of the soil samples. Correlations between trace elements and macronutrients provide some information about fertilisation practices and heavy metal sources.A limited number of soils showed slightly enhanced levels for As, Be, Cu, Co, Cr Mn, Ni Pb and Zn. In most cases, this could be linked to the regional industrial activities. However, a clear increase for Cu and Zn, above the natural background could be distinguished in areas with low atmospheric heavy metal deposits. In these cases, the excessive use of animal manure in the past may be the reason for this enrichment. However there was no indication that the Cd content of the soil was raised by the use of large amounts of pig slurry and/or by other common agricultural activities.

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.

Fourteen species of wild growing mushrooms and surface (0–10 cm) soils were collected near Lake Wdzydze in the northern part of Poland in 1996–1997 to understand the status of mercury pollution. Concentrations of mercury in mushrooms varied between 100±30 and 2400±1900 ng g⁻¹dry matter in caps and 60±1 and 1300±1500 ng g⁻¹dry matter in stalks. Concentrations of mercury in underlying soil were between 30±1 and 140±120 ng g⁻¹dry matter (between 36±18 and 63±100 ng g⁻¹depending on the soil type). Bioconcentration factors (BCF: concentrations in mushroom/concentrationin soil) of total mercury were between 2.3±1.1 and 90±110 for caps, and between 2.1±1.0 and 53±56 for stalks. Scaly tooth (Sarcodon imbricatum) contained the greatest concentrations of mercury in the flesh. However, there was no significant relationship (p >: 0.05) between mercury content in the fruiting bodies of this speciesto soil mercury concentrations. A significant (p < 0.01) positive relationship between mercury content in caps to underlying soil was noted for European cow bolete (Suillus bovinus), while a negative relationship between mercury content in caps and stalks to underlying soil was observed for Sandy knight-cap (Tricholomaflavovirens), Shaggy scale-head (Pholiota squaroso-adiposa),Gypsy mushroom (Rozites caperata) and Pine spike cap (Chroogomphus rutilus).

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.

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.