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 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.

Groundwater in the Rio de las Avenidas sub-basin corresponds to the bicarbonate-sodium and bicarbonate-calcium hydrochemical facies, which result from the mineralization of water passing through alkaline rocks (andesites) which prevail in this basin. However, the presence of high concentrations of Na⁺ and K⁺ reveals the existence of an external inflow of these elements: the registered mean values are respectively 94.3 and 19.0 ppm, with the Tèllez and Tizayuca areas standing out with reported values of up to 142 ppm. As for the concentration of soluble water cations, we find in decreasing order: Na⁺, Ca²⁺, Mg²⁺, K⁺, along with the anions HCO₃ ⁻, Cl⁻, SO₄ ²⁻, CO₃ ⁻, which combine to form the NaHCO₃, NaCl, Ca(HCO₃)₂, MgSO₄ and KCl salts. The presence of biological contaminants, P and detergents in the groundwater indicates that it may have been contaminated by waste water. In addition to the contaminants mentioned above, large quantities of Pb, B, Zn, Fe, Mn, Cr, Co were detected and although Fe, Pb, Zn, B, and Mn are closely related to the local lithology, the high concentrations of these elements along with the occurrence of Co, Cr, Cd, and Ni confirm the gradual degradation of the aquifers in the sub-basin. The water temperature indicates the existence of low temperature thermal processes in the area.