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Traditionally, the monitoring of streams for chemical and ecological status has been limited to surface water concentrations, where the dominant focus has been on general water quality and the risk for eutrophication. Mixed land use stream systems, comprising urban areas and agricultural production, are challenging to assess with multiple chemical stressors impacting stream corridors. New approaches are urgently needed for identifying relevant sources, pathways and potential impacts for implementation of suitable source management and remedial measures. We developed a method for risk assessing chemical stressors in these systems and applied the approach to a 16-km groundwater-fed stream corridor (Grindsted, Denmark). Three methods were combined: (i) in-stream contaminant mass discharge for source quantification, (ii) Toxic Units and (iii) environmental standards. An evaluation of the chemical quality of all three stream compartments - stream water, hyporheic zone, streambed sediment - made it possible to link chemical stressors to their respective sources and obtain new knowledge about source composition and origin. Moreover, toxic unit estimation and comparison to environmental standards revealed the stream water quality was substantially impaired by both geogenic and diffuse anthropogenic sources of metals along the entire corridor, while the streambed was less impacted. Quantification of the contaminant mass discharge originating from a former pharmaceutical factory revealed that several 100 kgs of chlorinated ethenes and pharmaceutical compounds discharge into the stream every year. The strongly reduced redox conditions in the plume result in high concentrations of dissolved iron and additionally release arsenic, generating the complex contaminant mixture found in the narrow discharge zone. The fingerprint of the plume was observed in the stream several km downgradient, while nutrients, inorganics and pesticides played a minor role for the stream health. The results emphasize that future investigations should include multiple compounds and stream compartments, and highlight the need for holistic approaches when risk assessing these dynamic systems.
Users may download and print one copy of any publication from the public portal for the purpose of private study or research. You may not further distribute the material or use it for any profit-making activity or commercial gain You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.
Contaminant mass discharge is a commonly applied tool to evaluate the environmental impact of contaminated sites on water resources. At large contaminated sites with heterogeneous sources, such as landfills, the number of wells available is often not sufficient, leading to a high uncertainty of mass discharge estimates. In this study, we tackle the uncertainty of the contaminant mass discharge due to low sampling densities by interpolating limited water‐sample data with the support of surface direct current resistivity and induced polarization geophysical data. The method relies on finding a conceptual link between the bulk conductivity imaged from geophysics and the contaminant concentrations. We investigate the link between (1) imaged bulk and electrical water conductivity, (2) water conductivity and conservative ionic species, (3) water conductivity and redox‐sensitive species, (4) water conductivity and semipersistent organic species, and (5) water conductivity and biodegradable organic compounds. The method successfully identify similarities between the distribution of the bulk conductivity and chloride and pharmaceutical compounds in a landfill leachate plume and between the bulk conductivity data and benzene and chlorinated ethenes for a contaminant plume from a former pharmaceutical factory. Contaminant concentrations were interpolated through regression kriging, using geophysical data as the dependent variable. The distribution of concentration determined with the novel method showed a lower mean relative estimation error than the traditional method of kriging only contaminant concentration data. At large sites, the method can improve contaminant mass discharge estimates, especially if surface geophysical measurements are integrated in the site investigation at an early stage.
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