Soils in lakes: the impact of inundation and storage on surface water quality

Jos P.M. Vink*, Rob N.J. Comans, Joris J. Dijkstra, Leon P.M. Lamers

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The large-scale storage and inundation of contaminated soils and sediments in deep waterlogged former sand pits or in lakes have become a fairly common practice in recent years. Decreasing water depth potentially promotes aquatic biodiversity, but it also poses a risk to water quality as was shown in a previous study on the impact on groundwater. To provide in the urgent need for practical and robust risk indicators for the storage of terrestrial soils in surface waters, the redistribution of metals and nutrients was studied in long-term mesocosm experiments. For a range of surface water turbidity (suspended matter concentrations ranging from 0 to 3000 mg/L), both chemical partitioning and toxicity of pollutants were tested for five distinctly different soils. Increasing turbidity in surface water showed only marginal response on concentrations of heavy metals, phosphorus (P) and nitrogen (N). Toxicity testing with bioluminescent bacteria, and biotic ligand modelling (BLM), indicated no or only minor risk of metals in the aerobic surface water during aerobic mixing under turbid conditions. Subsequent sedimentation of the suspended matter revealed the chemical speciation and transport of heavy metals and nutrients over the aerobic and anaerobic interface. Although negative fluxes occur for Cd and Cu, most soils show release of pollutants from sediment to surface waters. Large differences in fluxes occur for PO4, SO4, B, Cr, Fe, Li, Mn and Mo between soils. For an indicator of aerobic chemical availability, dilute nitric acid extraction (0.43 M HNO3; Aqua nitrosa) performed better than the conventional Aqua regia destruction. Both the equilibrium concentrations in surface waters, and fluxes from sediment, were adequately (r2 = 0.81) estimated by a 1 mM CaCl2 soil extraction procedure. This study has shown that the combination of 0.43 M HNO3 and 1 mM CaCl2 extraction procedures can be used to adequately estimate emissions from sediment to surface waters, and assess potential water quality changes, when former sand pits are being filled with soil materials.

Original languageEnglish
Article number339
JournalEnvironmental Monitoring and Assessment
Volume192
Issue number6
DOIs
Publication statusPublished - Jun 2020

Keywords

  • Bioavailability
  • Biotic ligand models
  • Chemical extraction
  • Risk assessment
  • Sediment fluxes
  • Speciation
  • Suspended matter
  • Toxicity

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