No abstract

Soils containing an approximately equal mixture of metastable iron sulfides and pyrite occur in the boreal Ostrobothnian coastal region of Finland, termed ‘potential acid sulfate soil materials’. If the iron sulfides are exposed to air, oxidation reactions result in acid and metal release to the environment that can cause severe damage. Despite that acidophilic microorganisms catalyze acid and metal release from sulfide minerals, the microbiology of acid sulfate soil (ASS) materials has been neglected. The molecular phylogeny of a depth profile through the plough and oxidized ASS layers identified several known acidophilic microorganisms and environmental clones previously identified from acid- and metal-contaminated environments. In addition, several of the 16S rRNA gene sequences were more similar to sequences previously identified from cold environments. Leaching of the metastable iron sulfides and pyrite with an ASS microbial enrichment culture incubated at low pH accelerated metal release, suggesting microorganisms capable of catalyzing metal sulfide oxidation were present. The 16S rRNA gene analysis showed the presence of species similar to Acidocella sp. and other clones identified from acid mine environments. These data support that acid and metal release from ASSs was catalyzed by indigenous microorganisms adapted to low pH.

No abstract

Some of the most economically valued soils for agricultural use are naturally occurring sulfide rich sediments. However, formation of acid sulfate soils with sulfuric materials (pH 4) can occur when sulfidic materials are exposed to air, which can then result in mobilisation of large amounts of acid and metals into nearby water bodies. In this study, controlled drainage, subsurface irrigation and hydrochemical precision treatments are combined to reduce acidic discharges on a novel project field in western Finland. The PRECIKEM project field consists of nine identical hydrologically isolated 1 ha subfields. Each field had a drainage system consisting of three subsurface drainage pipes (c. 1.3 m deep), a collector pipe, and a control well enabling manual groundwater table management. Utilising such drainage installations already common on farmlands, suspensions of fine-grained (d 50 = 2.5 µm) calcium carbonate and/or calcium hydroxide were pumped in to control wells in order to be distributed in to subsoils with sulfuric materials via drainage networks with the aim to: (1) neutralise acidity, (2) inhibit microbially mediated sulfide oxidation and (3) immobilise metals. The discharge waters from the fields were monitored during the project period 2012-2016. As is typical for acid sulfate soils with sulfuric materials, the discharge waters from the reference fields (n = 3) that had been treated with water only, had very low pH values ( 4) and the acidity and concentrations of several metals were up to two magnitudes higher than the average in Finnish stream waters. Excavation of selected treated fields revealed the calcium carbonate to have formed a neutralising coating on the surfaces of hydrologically active macropores in the soil matrix near the subsurface drainage pipes. This effectively resulted in a long-term (1-4 years) situation of raised pH, lower acidity and lower concentrations of several acid sensitive metals, most prominently a significant decrease (> 90%) in Al concentrations. Fe concentrations in discharge waters were subsequently decreased as the predominance of Fe shifted toward the schwertmannite and iron oxides stability phases due to changes in pH/redox conditions. The methods presented in this work showed favourable steps toward environmentally sustainable agriculture and improving the chemical and ecological status of acid sulfate soil affected coastal waters.

No abstract