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Decline in Performance of Biochemical Reactors for Sulphate Removal from Mine-Influenced Water is Accompanied by Changes in Organic Matter Characteristics and Microbial Population Composition

Multidisciplinary Digital Publishing Institute

Successful long-term bioremediation of mining-influenced water using complex organic matter and naturally-occurring microorganisms in sub-surface flow constructed wetlands requires a balance between easily and more slowly degrading material. This can be achieved by combining different types of organic materials. To provide guidance on what mixture combinations to use, information is needed on how the ratio of labile to recalcitrant components affects the degradation rate and the types of microbial populations supported. To investigate this, different ratios of wood and hay were used in up-flow column bioreactors treating selenium- and sulphate-containing synthetic mine-influenced water. The degradation rates of crude fibre components appeared to be similar regardless of the relative amounts of wood and hay. However, the nature of the degradation products might have differed in that those produced in the hay-rich bioreactors were more biodegradable and supported high sulphate-reduction rates. Microorganisms in the sulphate-reducing and cellulose-degrading inocula persisted in the bioreactors indicating that bio-augmentation was effective. There was a shift in microbial community composition over time suggesting that different microbial groups were involved in decomposition of more recalcitrant material. When dissolved organic carbon (DOC) was over-supplied, the relative abundance of sulphate-reducers was low even through high sulphate-reduction rates were achieved. As DOC diminished, sulphate-reducers become more prevalent and their relative abundance correlated with sulphate concentrations rather than sulphate-reduction rate.

Article

eng

Vancouver : University of British Columbia Library

10.14288/1.0378164

Applied Science, Faculty of; Chemical and Biological Engineering, Department of

10.3390/w8040124

Faculty

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