Predicting the impact and duration of persistent and mobile organic compounds in groundwater systems using a contaminant mass discharge approach.

This study investigated methods for predicting the duration and impact on groundwater quality from persistent and mobile organic compounds (PMOCs) at a drinking water well field affected by multiple contaminant sources. The fungicide metabolite N,N-dimethylsulfamide (DMS), which frequently occurs above the Danish groundwater quality criterion (0.1 µg/L), was used as an example. By combining contaminant mass discharge (CMD) estimations, modeling, and groundwater dating, a number of important discoveries were made. The current center of contaminant mass was located near the source area. The CMD at the well field was predicted to peak in 2040, and an effect from the investigated sources on groundwater quality could be expected until the end of the 21st century. A discrepancy in the current CMD at the well field and the estimated arrival time from the studied source area suggested an additional pesticide source, which has not yet been thoroughly investigated. The presence of the unknown source was supported by model simulations, producing an improved mass balance after inclusion of a contaminant source closer to the well field. The approach applied here was capable of predicting the duration and impact of DMS contamination at a well field at catchment scale. It furthermore shows potential for identification and quantification of the contribution from individual sources, and is also applicable for other PMOCs. Predicting the duration of the release and impact of contaminant sources on abstraction wells is highly valuable for water resources management and authorities responsible for contaminant risk assessment, remediation, and long-term planning at water utilities.

Long-term leaching through clayey till of N,N-dimethylsulfamide, a Persistent and Mobile Organic Compound (PMOC).

Environmental pollution with Persistent and Mobile Organic Compounds (PMOC) from anthropogenic activities is an increasing cause for concern. These compounds are readily leached to groundwater aquifers and are likely to resist degradation, putting pressure on groundwater resources. Pesticides can form PMOCs upon degradation in the environment. The PMOC N,N-dimethylsulfamide (DMS) was the most frequently detected pesticide metabolite in Danish drinking water wells in 2020, although the pesticidal use of the last parent compound (tolylfluanid) ended in 2007. This study aimed to improve the understanding of the leaching of the PMOC DMS from clayey tills by combining a review of compound properties, sources and use, comprehensive field observations and numerical flow and solute transport modeling. The modeling explored the mechanisms of DMS retention during vertical transport in clayey till and the fingerprint in the underlying aquifer. The results were supported by detailed field observations at an agricultural site with strawberry production. Porewater samples were collected from clayey till to a depth of 12 m bgs by a custom designed installation method of suction cups. Groundwater sampling (249 samples) was designed to provide vertical concentration profiles at various distances from the presumed sources. The review of properties showed that the parent compounds and intermediates degrade quickly in topsoil, releasing the highly persistent and mobile DMS. We tested the effect of fractures on transport with different hydraulic apertures and a scenario without fractures by numerical modeling. The results showed that the presence of fractures can smooth the breakthrough curve below the clayey till, leading to faster breakthrough, lower maximum concentration, and several decades of prolonged leaching in simulations with the largest aperture (20 µm). The fracture-matrix interaction is a possible explanation for the observed delay of leaching from clayey till. The vertical concentration profiles in groundwater were used for identifying the sources at the field site and testing source strengths. Assigning one point source (200 µg/L) and two diffuse sources (40-50 µg/L) to the model produced vertical concentration profiles that compared well with observed field data in clayey till and the aquifer. All results were integrated into a conceptual model for the environmental fate of PMOCs in soil and groundwater. The findings of this study imply that the presence of fractures in clayey till should be considered in conceptual site models, since they can substantially prolong the leaching of PMOCs to groundwater. The integration of comprehensive field investigations and numerical modeling is key to understand the fate of PMOCs in complex field systems with different source types. Together with widespread occurrences of PMOCs in groundwater systems, the results highlight the need for improved approval procedures for pesticides and biocides which considers their persistent and mobile metabolites.

Sorption and degradation of the herbicide 2-methyl-4,6-dinitrophenol under aerobic conditions in a sandy aquifer in Vejen, Denmark.

A pulse (7 days) and a continuous (216 days), natural gradient field injection experiment with herbicides, including 2-methyl-4,6-dinitrophenol (4,6-dinitro-o-cresol, abbreviated DNOC), and a bromide tracer were conducted in a shallow, aerobic aquifer near Vejen, Denmark. The pulse and continuous plume were monitored in a dense, three-dimensional monitoring network installed in the aquifer downgradient of the injection. The sorption and degradation of DNOC were evaluated based on moment analysis of breakthrough curves, cross sections, and snapshots of the DNOC plume and supported by results from laboratory experiments. Significant and spatially variable sorption of DNOC (Kd range, 0.10-0.98 L/kg) was observed due to a specific binding of DNOC to clay minerals. The spatial variation was mainly a result of variation in pH, with stronger sorption at lower pH, whereas other factors such as cation composition on the solid matrix appeared to be negligible. Significant degradation of DNOC in the aquifer was revealed by moment analysis of data from the continuous field injection experiment. Degradation of DNOC in the field was slow and/or subject to long lag phases, and the data suggested spatially varying degradation potentials. This was supported by the laboratory experiments. The potential for natural attenuation of DNOC in aerobic aquifers appears promising.

Fate of seven pesticides in an aerobic aquifer studied in column experiments.

The fate of selected pesticides (bentazone, isoproturon, DNOC, MCPP, dichlorprop and 2,4-D) and a metabolite (2,6-dichlorobenzamide (BAM)) was investigated under aerobic conditions in column experiments using aquifer material and low concentrations of pesticides (approximately 25 microg/l). A solute transport model accounting for kinetic sorption and degradation was used to estimate sorption and degradation parameters. Isoproturon and DNOC were significantly retarded by sorption, whereas the retardation of the phenoxy acids (MCPP, 2,4-D and dichlorprop), BAM and bentazone was very low. After lag periods of 16-33 days for the phenoxy acids and 80 days for DNOC, these pesticides were degraded quickly with 0.-order rate constants of 1.3-2.6 microg/l/day. None of the most probable degradation products were detected.