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 ten year survey of water quality in 330 Massachusetts streams was conducted to examine the rate and pattern of recovery from acidification. Meta-analysis was used to combine the results of the 330 non-parametric trend tests into an overall test for trend in a variety of water quality variables including pH, acid neutralizing capacity (ANC), and major inorganic ions. Analysis of trends in the raw data indicates both pH and ANC are increasing. After detrending for variations in stream runoff, we estimate the streams are recovering from acidification at a rate of +0.021 pH units/year and +2.4μeq/L/year, for pH and ANC respectively. These trends appear to be related to declines in sulfate (−1.8μeq/L/year), while base cation trends were mixed. Meta-analysis reveals the trends are not always homogeneous between seasons or between sites.While it is commonly assumed that the low ANC systems are most ‘sensitive’ to changes in acid or base inputs, we found the greatest rates of change in ANC were associated with the high ANC systems. The greatest increases in pH were seen in the low ANC streams as expected. The results also suggest streams respond quickly to changes in precipitation inputs and stream monitoring networks may be valuable as an early detection technique for changes in environmental quality.

A total of 51 lakes in southern Quebec, Canada, were sampled between 1985 and 1993 to study changes in water chemistry following reductions in SO₂ emissions (main precursor of acid precipitation). Time series analysis of precipitation chemistry revealed significant reductions in concentrations and deposition of SO₄ ²⁻ from 1981 to 1992 in southern Quebec as well as reductions in concentrations and deposition of base cations (Ca²⁺, Mg²⁺), NO₃ ⁻ and H⁺ in the western section of the study area. Reductions in atmospheric inputs inputs of SO₄ ²⁻ have resulted in decreased lakewater SO₄ ²⁻ concentrations in the majority of the lakes in our study, although only a small fraction (9 of 37 lakes used in the temporal analysis) have improved significantly in terms of acidity status (pH, acid neutralizing capacity — ANC). The main response of the lakes to decreased SO₄ ²⁻ is a decrease in base cations (Ca²⁺+Mg²⁺), which was observed in 17 of 37 lakes. Seventeen lakes also showed significant increases in dissolved organic carbon (DOC) over the period of study. The resulting increases in organic acidity as well as the decrease in base cations could both play a role in delaying the recovery of our lakes.