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.

This paper reports on magnetic and magnetomineralogical studies of forest soils from Krkonoše (Giant Mountains) National Park in the Czech Republic. Low-field magnetic susceptibility was measured in 32 soil profiles using a field probe. Thermomagnetic analysis, acquisition of remanent magnetization, alternating-field demagnetization of saturation remanence and frequency-dependent magnetic susceptibility were measured in laboratory samples from individual soil horizons as well as on their magnetic extracts. X-ray diffraction and SEM were used to identify ferrimagnetic fractions. The uppermost layer, which is dominated by magnetically soft magnetite of presumably anthropogenic origin, can be reliably identified in soil profiles over the whole region of concern. Subsoil horizons are characterised by significantly different magnetic properties.

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.

Assessing metal contamination of sediments requires knowledge of the geochemical partitioning of trace metals at the sediment-water interface. Under controlled laboratory conditions, sequential extraction was conducted to determine the associations of metals (Cd, Cr, and Zn) and radiotracers (¹⁰⁹Cd,⁵¹Cr, and⁶⁵Zn) with various geochemical phases and the different partitioning and mobility of metals for two types of surface sediments collected from the Huanghe and Changjiang Rivers in Eastern China. The residual phase was the major phase for stable metal binding, indicating that these sediments had little subjection to recent anthropogenic influences. Fe–Mn oxides were the next important binding phases for metals. The partitioning of metals in various geochemical phases as a function of the duration of the radiolabeling was also examined. Trace metals transferred among the different geochemical phases over the 30 days radiolabeling period, particularly between the carbonate and Fe–Mn oxides phases. The freshwater-sediment distribution coefficients (Kd) of three metals were investigated in batch experiments using the radiotracer technique. The decreasing Kdwith increasing metal concentration(from 0.5 to 200 μg L⁻¹) may be explained by competitive adsorption. The metal Kdin sediments from the Changjiang River was greater than those from the Huanghe River, presumably because of the higher Fe/Mn and organic carbon contents in Changjiang River sediment. The Kddecreased with increasing total suspended solid load from 3 to 500 mg L⁻¹, and was Cr > Zn > Cd. For Cd and Zn, increasing the pH from 5 to 8 resulted in an increase in Kddue to the reduced H⁺competition and increasing sorptionpotential. However, the Kdfor Cr in the sediments from both rivers showed no relationship with pH, presumably becauseof the complexity of the Cr species and environmental behavior.