• Title of article

    Isotopic modelling of the significance of bacterial sulphate reduction for phenol attenuation in a contaminated aquifer

  • Author/Authors

    Michael J. Spence، نويسنده , , Simon H. Bottrell، نويسنده , , Steven F. Thornton، نويسنده , , David N. Lerner ، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2001
  • Pages
    20
  • From page
    285
  • To page
    304
  • Abstract
    A Triassic sandstone aquifer polluted with a mixture of phenolic hydrocarbons has been investigated by means of high-resolution groundwater sampling. Samples taken at depth intervals of 1 m have revealed the presence of a diving pollutant plume with a sharply defined upper margin. Concentrations of pollutant phenols exceed 4 g/l in the plume core, rendering it sterile but towards the diluted upper margin evidence for bacterial sulphate reduction (BSR) has been obtained. Groundwaters have been analysed for both δ34S–SO4 and δ18O–SO4. Two reservoirs have been identified with distinct sulphate–oxygen isotope ratios. Groundwater sulphate (δ18O–SO4=3–5‰) outside the plume shows a simple linear mixing trend with an isotopically uniform pollutant sulphate reservoir (δ18O–SO4=10–12‰) across the plume margin. The sulphur isotope ratios do not always obey a simple mixing relation, however, at one multilevel borehole, enrichment in 34SO4 at the plume margin is inversely correlated with sulphate concentration. This and the presence of 34S-depleted dissolved sulphide indicate that enrichment in 34SO4 is the result of bacterial sulphate reduction. δ34S analysis of trace hydrogen sulphide within the plume yielded an isotope enrichment factor ( ) of −9.4‰ for present-day bacterial sulphate reduction. This value agrees with a long-term estimate (−9.9‰) obtained from a Rayleigh model of the sulphate reduction process. The model was also used to obtain an estimate of the pre-reduction sulphate concentration profile with depth. The difference between this and the present-day profiles then gave a mass balance for sulphate consumption. The organic carbon mineralisation that would account for this sulphate loss is shown to represent only 0.1‰ of the phenol concentration in this region of the plume. Hence, the contribution of bacterial sulphate reduction to biodegradation has thus far been small. The highest total phenolic concentration (TPC) at which there is sulphur isotope evidence of bacterial sulphate reduction is 2000 mg/l. We suggest that above this concentration, the bactericidal properties of phenol render sulphate-reducing bacteria inactive. Dissolved sulphate trapped in the concentrated plume core will only be utilised by sulphate reducers when toxic phenols in the plume are diluted by dispersion during migration.
  • Keywords
    stable isotopes , Bacterial sulphate reduction , natural attenuation , Organic pollutants , Phenol toxicity
  • Journal title
    Journal of Contaminant Hydrology
  • Serial Year
    2001
  • Journal title
    Journal of Contaminant Hydrology
  • Record number

    693256