Short- and Long-Term Effects of Lime and Gypsum Applications on Acid Soils in a Water-Limited Environment: 3. Soil Solution Chemistry

Aluminum (Al) toxicity imposes a significant limitation to crop production in South Western Australia. This paper examines the impact of surface-applied lime and gypsum on soil solution chemistry in the short term (1 year) and the long-term (10 years) in water limited environments. In the experiments, we measured soil solution chemistry using a paste extract on soil profile samples collected to a depth of 50 cm. We then used the chemical equilibrium model MINTEQ to predict the presence and relative concentrations of Al species that are toxic to root growth (Al associated with Al3+ and AlOH2 or Toxic-Al) and less non-toxic forms of Al bound with sulfate, other hydroxide species and organic matter. A feature of the soils used in the experiment is that they have a low capacity to adsorb sulfate. In the short term, despite the low amount of rainfall (279 mm), sulfate derived from the surface gypsum application is rapidly leached into the soil profile. There was no self-liming effect, as evidenced by there being no change in soil solution pH. The application of gypsum, in the short term, increased soil solution ionic strength by 524–681% in the 0–10 cm soil layer declining to 75–109% in the 30–40 cm soil layer due to an increase in soil solution sulfate and calcium concentrations. Calcium from the gypsum application displaces Al from the exchange sites to increase soil solution Al activity in the gypsum treatments by 155–233% in the short term and by 70–196% in the long term to a depth of 40 cm. However, there was no effect on Toxic-Al due to Al sulfate precipitation. In the long term, sulfate leaching from the soil profile results in a decline in soil solution ionic strength. Application of lime results in leaching of alkalinity into the soil profile leading to a decreased Toxic-Al to a depth of 30 cm in the long term, but it did not affect Toxic-Al in the short term. Combining an application of lime with gypsum had the same impact on soil solution properties as gypsum alone in the short term and as lime alone in the long term.

Spatially resolved soil solution chemistry in a central European atmospherically polluted high-elevation catchment

We collected soil solutions by suction lysimeters in a central European temperate forest with a history of acidification-related spruce die-back in order to interpret spatial patterns of soil nutrient partitioning, compare them with stream water chemistry and evaluate these parameters relative to concurrent loads of anions and cations in precipitation. Five lysimeter nests were installed in the 33 ha U dvou loucek (UDL) mountain catchment at different topographic positions (hilltops, slopes and valley). Following equilibration, monthly soil solution samples were interrogated over a 2-year period with regard to their SO42-, NO3-, NH4+, Na+, K+, Ca2+, Mg2+ and total dissolved Al concentrations, organic carbon (DOC) and pH. Soil pits were excavated in the vicinity of each lysimeter nest to also constrain soil chemistry. For an estimation of phosphorus (P) availability, ammonium oxalate extraction of soil samples was performed. Cation exchange capacity (CEC ≤58 meq kg−1) and base saturation (BS ≤13 %) were found to be significantly lower at UDL than in other monitored central European small catchments areas. Spatial trends and seasonality in soil solution chemistry support belowground inputs from mineral-stabilized legacy pollutants. Overall, the soil solution data suggest that the ecosystem was still chemically out of balance relative to the concurrent loads of anions and cations in precipitation, documenting incomplete recovery from acidification. Nearly 30 years after peak acidification, UDL exhibited similar soil solution concentrations of SO42, Ca2+ and Mg2+ as median values at the Pan-European International Co-operative Program (ICP) Forest sites with similar bedrock lithology and vegetation cover, yet NO3- concentrations were an order of magnitude higher. When concentrations of SO42-, NO3- and base cations in runoff are compared to soil pore waters, higher concentration in runoff points to lateral surficial leaching of pollutants and nutrients in excess than from topsoil to subsoil. With P availability being below the lowest range observed in soil plots from the Czech Republic, the managed forest ecosystem in UDL probably reflects growing inputs of C from regenerating vegetation in the N-saturated soil, which leads to P depletion in the soil. In addition, the observed spatial variability provides evidence pointing to substrate variability, C and P bioavailability, and landscape as major controls over base metal leaching toward the subsoil level in N-saturated catchments.