Wood cores were taken at breast height of mature sugar maple (Acer Saccharum Marsh.) trees of approximately the same age from four sites in Ontario, Canada differing in soil characteristics and general tree health. The soils of two of the sites were acidic (podzols), while the soils of the other two sites were calcareous (brunisols). Selected elemental analyses using Neutron Activation Analysis were conducted on the soils and the xylem wood of the sugar maple trees, and the results were compared relative to tree health. Aluminum in stem xylem was found to be significantly higher in declining trees (mean 7.7 ppm) relative to the healthy trees (mean 4.0) from the acidic sites, where aluminum was freely available in the soil. Soil extractable aluminum was also significantly higher in the soil adjacent to the declining trees (mean 5.10) compared to the healthy trees (mean 3.20). These results show that xylem aluminum contents reflect the increased availability of aluminum in acidifying soils and provide additional evidence that dendrochemistry may be used as a proxy environmental monitoring tool.

A field study was performed on the effects of acid mine leachate from slate mine tailings seeping into a small river passing through the tailings. Before entering the tailings the river water has high alkalinity which neutralizes acidity upon mixing with leachate within the tailings. Donwstreams of the tailings the pH of the river water ranges about pH = 8, the water contains high concentrations of sulfate (≈1500 μmol/1 and particulate bound aluminium (≈80 μmol/I), but low concentrations of dissolved aluminium (≈3 μmol/1). It is therefore assumed that AI(OH)₃ colloids are precipitated during the neutralisation process and transported out of the tailings. The concentration of particulate bound aluminium along the river shows a strong correlation with the concentration of sulfate, which indicates that particulate bound aluminium is conservative. It therefore seems that under dry weather conditions (under most of the sampling was performed) no chemical retention mechanism exists which confines the distribution of aluminium to a restricted part of the catchment area. In contrast, the white river sediment is rich in both aluminium and sulfate, which suggests the temporary formation of aluminium hydroxosulfate minerals. Favorable (i.e. acidic) conditions may prevail at high discharges where the acidity accumulated in the tailings is flushed into the river with its subsequent acidification.

A new plastic-lined high-pressure squeezing device has been developed for the extraction of soil pore solutions. At a maximum pressure of 1100 kg cm⁻² the water recovery ranged between 30 and 55% of the total water content. Pressure dependent squeezing experiments showed a general increase in Si, Mn, Mg, Ca, K, Na, Al, Fe, Cd, and Zn concentrations with progressive pore water extraction and increasing pressure, indicating that micro pore solutes have the highest concentrations of solutes. Soil samples with moisture contents of more than about 15% generally provided enough water for major and trace element analyses. The data do not reveal any contamination of the pore fluids from the squeezing device. An advantage of this method is that the solution could be closely related to a specific soil horizon on a cm scale and also to the time of sampling. A further application of this squeezing method is the possibility of pressure dependent sequential squeezing to obtain fluids from different pore spaces.

The effects of chemical speciation on mineralization of organic compounds was studied using citric acid as a model substance. The degradation of ¹⁴C-labeled Al-, Co-, Cu-, and Zn-citrate was followed in chemically well-defined media inoculated with mixed cultures of microorganisms (soil extracts from two soils). The degradation of citrate was completely inhibited when the acid was bound to Zn, Cu, or Co and partly inhibited when bound to Al. The mineralization of citrate as well as histidine was also followed by incubation of the complexes (Cu, Zn, Al) in the two soils. No effect of metals on the degradation of histidine was seen. The degradation of citrate in soils was also unaffected when complexed to Cu and Zn, whereas Al exerted an inhibited decomposition in both soils.

Sandy soils, in the border area of Belgium and the Netherlands (the Kempen region), are heavily contaminated by atmospheric deposition of cadmium and zinc from nearby smelters. Groundwater contamination by leaching from these low retention soils is subject of study. There are reports of high cadmium and zinc concentrations in groundwater in the area, but in most cases the direct sources are unknown. In an attempt to predict present or future risk of groundwater contamination by soil leaching, metal binding processes (retardation) were studied that are specific for these soil types under the existing acidifying conditions. From four fields nine contaminated profiles were sampled and analyzed for cadmium and zinc. Average concentrations of 131μg g⁻¹ zinc and 1.6μg g⁻¹ cadmium with maximum values of 2989μg g⁻¹ respectively 16.3μg g⁻¹ were found. In addition pH and contents of organic matter, aluminium, iron, and manganese were determined. The relative importance of these soil parameters for metal retardation is derived from the profiles. The data show that organic matter is the most important soil component for binding cadmium and zinc. Adsorption of cadmium and zinc on aluminium, iron and manganese (hydr) oxides appears to be of minor importance at low pH (<5.5).

The foliage contents of Sₜₒₜₐₗ and Nₜₒₜₐₗ were determined in 405 Permanent monitoring plots in four National Parks and sixteen Landscape Protection Areas and were compared with 1483 Permanent monitoring plots on Slovakia. The foliage content of S ranged from 0.72 to 6.77 g kg⁻¹ in hardwoods and from 0.98 to 4.3 g kg⁻¹ in softwoods. A critical increase was determined in one National Park and in four Landscape Protection Areas. The foliage content of N ranged from 9.7 to 48.7 g kg⁻¹ in softwoods, and from 7.8 to 51.4 g kg⁻¹ in hardwoods. An insufficient level of N was determined in one Landscape Protection Area and a critical increase in four Landscape Protection Areas. The sulphur to nitrogen ratio ranged from 0.08 to 0.176 in softwoods, and from 0.078 to 0.253 in hardwoods. The foliage surface on hitherto explored four National Parks and sixteen Landscape Protection Areas in network 4×4 km was covered by all categories of rigid fallout particles. Fly-ash from coal combustion were observed each of National Parks and Landscape Protection Areas by scanning electron microscopy. Mycelia and spore, mineral matters, sand and soil particles were present on all National Parks and Landscape Protection Areas. Particles derived from aluminium production were observed at three Landscape Protection Areas. Particles derived from cement production and from lime works were observed at two National Parks and six Landscape Protection Areas. Particles derived from ferrous metals industry were observed at each of National Parks and Landscape Protection Areas and particles typical for other technologies were present in three of National Parks and twelve Landscape Protection Areas.

In June 1983 a whole-catchment liming experiment was conducted at Tjønnstrond, southernmost Norway, to test the utility of terrestrial liming as a technique to restore fish populations in remote lakes with short water-retention times. Tjønnstrond consists of 2 small ponds of 3.0 and 1.5 ha in area which drain a 25-ha catchment. The area is located at about 650–700 meters above sea-level in sparse and unproductive forests of spruce, pine and birch with abundant peatlands. A dose of 3 ton/ha of powdered limestone were spread by helicopter to the terrestrial area. No limestone was added to the ponds themselves. The ponds were subsequently stocked with brown and brook trout.Liming caused large and immediate changes in surface water chemistry; pH increased from 4.5 to 7.0, Ca increased from 40 to 200μeq/L, ANC increased from −30 to +70μeq/L, and reactive-Al decreased from about 10 to 3μmol/L. During the subsequent 11 years the chemical composition of runoff has decreased gradually back towards the acidic pre-treatment situation. The major trends in concentrations of runoff Ca, ANC, pH, Al and NO₃ in runoff are all well simulated by the acidification model MAGIC. Neither the measured data nor the MAGIC simulations indicate significant changes in any other major ion as a result of liming.The soils at Tjønnstrond in 1992 contained significantly higher amounts of exchangeable Ca relative to those at the untreated reference catchment Storgama. In 1992 about 75% of the added Ca remains in the soil as exchangeable Ca, 15% has been lost in runoff, and 10% is unaccounted for.The whole-catchment liming experiment at Tjønnstrond clearly demonstrates that this liming technique produces a long-term stable and favourable water quality for fish. Brown trout in both ponds in 1994 have good condition factors, which indicate that the fish are not stressed by marginal water quality due to re-acidification. The water quality is still adequate after 11 years and >20 water renewals. Concentrations of H⁺ and inorganic Al have gradually increased and approach levels toxic to trout, but the toxicity of these are offset by the continued elevated Ca concentrations. Reduced sulphate deposition during the last 4 years (1990–94) has also helped to slow and even reverse the rate of reacidification. The experiment at Tjønnstrond demonstrates that for this type of upland, remote terrain typical of large areas of southern Norway, terrestrial liming offers a suitable mitigation technique for treating acidified surface waters with short retention times.