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 study on the factors influencing nitrogen removal in waste water stabilization ponds was undertaken in an eight-pond series in Werribee, Australia. Nitrogen species including Kjeldahl nitrogen, total ammonia nitrogen, nitrite and nitrate were monitored monthly from March 1993 to January 1994. At the same time, pH, temperature, chlorophylla content and dissolved oxygen were also recorded. Highest nitrogen removal occurred during the period with highest levels of chlorophylla content and dissolved oxygen, but the rate of nitrogen removal was not related to temperature and pH. Enhanced photosynthetic activities resulting from an increased phytoplankton abundance due to prolonged detention time caused an increase in dissolved oxygen, and created an optimum condition for nitrification to occur. In this process, ammonia was oxidized to nitrite and nitrate which were subsequently reduced to elemental nitrogen. Apart from nitrification-denitrification which was the major nitrogen removal pathway in the study system, algal uptake of ammonium, nitrate and nitrite as nutrient sources also contributed to the nitrogen removal. The role of phytoplankton and zooplankton in the treatment process in waste stabilization ponds was discussed.

Certain blood morphology parameters: red blood cell (RBC) sizes; percentage of polymorphonuclear leukocytes and ratio polychromatocyte/RBC in Brown trout (Salmo trutta L.) from acidified water (mean pH value 4.94) and limed water (mean pH value 5.66) were investigated. The sizes of RBC long axises were significantly larger in fish from acidic environment than from limed condition (14.37 and 12.96μm respectively). The percentage of polymorphonuclear cells (7.86 and 3.32) and polychromatocyte/RBC ratio (0.079 and 0.019) were also significantly larger in fish from the acidified environment. Blood morphology parameters are concluded to be usefull for testing and detection of long-term acidic stress in fish in nature.

The influence of alkaline dust pollution (pH of water solution of dust 12.3–12.7) from a cement plant (Kunda town, Estonia) on chlorophylls and carotenoids of the needles of 60–80 year old Norway spruce was studied on sample plots established at different distances from the emission source. The highest sensitivity to dust impact was measured in the content of Chl a, Chl b, carotenoids and elements regulating or participating in the biosynthesis of pigments (Mg, Fe, N, Mn).

A study was carried out recently to determine the pollution level of waters in the Karachi harbour and adjoining backwaters. Nine locations were selected, four in the backwaters, two on the seaside, and three in the main navigable channel. Four of these locations were deliberately selected to coincide with those of a previous study conducted in 1982 by Pakistan Council of Scientific and Industrial Research (PCSIR) so that the values for the concentration of different pollutants could be compared. Analysis was conducted for pH, bicarbonates, Total Solids, Volatile matter in Total Solids, Chlorides, Sulphates, Calcium, Magnesium, Sodium and Potassium.The results indicate that the composition of sea water as far as the concentration of above constituents is concerned has not changed much since the time of the PCSIR study, viz 1982, except that the organic matter concentration has increased. The reasons for this increase in organic loading and its possible impact are discussed in this paper.

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.

The anaerobic conditions in landfill leachate-polluted aquifers can lead to trapping of many heavy metals as sulfide precipitates. In laboratory experiments with aqueous systems containing sulfidic solid phases (aquifer solids from a landfill leachate plume or amorphous FeS), cadmium previously trapped as a sulfide precipitate was released to the aqueous phase when conditions were changed from initially slightly anaerobic to aerobic. Cadmium was subsequently removed from solution either by adsorption on Fe oxyhydroxide phases or by precipitation as a carbonate mineral, groundwater pH being the major controlling variable.

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).

Base cation (Ca, Mg, Na, K) concentrations in surface waters, pore waters and surface peats were determined along a mineral-poor to mineral-rich fen gradient for 15 south-central Ontario peatlands. Surface waters of the peatlands ranged in pH and alkalinity from 4.5 to 6.3 and 0 to 181 μeqL⁻¹, respectively. Both surface water and pore water Ca and Mg concentrations followed the expected decrease along the mineral-rich to poor-fen gradient. Surface water concentrations of Ca and Mg were significantly lower in the mineral-poor versus the moderately-poor and mineral-rich fens (P <0.05, ANOVA). Pore water concentrations of base cations were 3–5 fold less in mineral-poor vs. mineral-rich fens. In contrast to surface and pore waters, peat base cation concentrations did not decrease along the mineral-rich to mineral-poor fen gradient. Surface peat base cation concentrations were also independent of pore water cation concentrations, and local bedrock geology. Relative concentrations of base cations in surface peats of all peatlands were best described by the exchangeable cation capacity of the surrounding soils.

A study was carried out recently to determine the pollution level of waters in the Karachi harbour and adjoining backwaters. Nine locations were selected, four in the backwaters, two on the seaside, and three in the main navigable channel. Four of these locations were deliberately selected to coincide with those of a previous study conducted in 1982 by Pakistan Council of Scientific and Industrial Research (PCSIR) so that the values for the concentration of different pollutants could be compared. Analysis was conducted for pH, bicarbonates, Total Solids, Volatile matter in Total Solids, Chlorides, Sulphates, Calcium, Magnesium, Sodium and Potassium.The results indicate that the composition of sea water as far as the concentration of above constituents is concerned has not changed much since the time of the PCSIR study, viz 1982, except that the organic matter concentration has increased. The reasons for this increase in organic loading and its possible impact are discussed in this paper.