Degradation of pesticides in aquifers has been evaluated based on a number of co-ordinated field and laboratory studies carried out in Danish aquifers. These studies included investigations of vertical and horizontal variability in degradation rates from the vadose zone to an aquifer, the effects of aerobic versus anaerobic conditions, and the importance of concentration on degradation kinetics for a selected range of herbicides. The studies were based on different experimental approaches ranging from simple batch experiments to column studies to field injection experiments and, where appropriate, results were compared. Some herbicides were degraded under aerobic conditions (some phenoxy acids, DNOC and glyphosate) and others under aerobic conditions (other phenoxy acids, DNOC; there was some indication of atrazine transformation). Certain pesticides were not degraded in any investigations (dichlobenil, the dichlobenil metabolite 2,6-dichlorobenzamide (BAM), bentazone, isoproturon, metamitron and metsulfuron-methyl). The spatial variability was substantial, since hardly any of the investigated pesticides were degraded in all comparable samples. This means that it is very difficult to claim that a given pesticide is readily degradable in aquifers. However, the experimental approaches used (with incubations lasting more than a year) may not be sensitive enough to verify the low degradation rates that may be significant as a result of the long retention time of groundwaters.
This paper presents data on the distribution of seven pesticides in an agricultural catchment which is located within the Agricultural Development and Advisory Service farm at Rosemaund, 11 km north‐east of Hereford, UK. Data for aldicarb, atrazine, carbofuran, dimethoate, MCPA and isoproturon, are available for both the soil and surface waters (drain and stream water), with simazine data available only for the stream. Measurements were taken before and after pesticide application, which was made following normal agricultural practice. Soil residue data showed the degradation rates of the pesticides to be within the range of literature values. Pesticide levels in the stream and drains during runoff events following rainfall ranged from below detection limits (typically 0.02‐0.1 μg/1), to 264 μg/1 (for carbofuran). Over 90% of the events had detectable maximum concentrations. The percentage of pesticide applied, which was removed during individual rainfall events, was calculated. The maximum value estimated was 1.1%, again for carbofuran. Most of the events gave values several orders of magnitude below this value.
The data have been used to try to validate a range of models which could be used for screening new pesticides or for informing decisions on the use of existing pesticides. The results of the validations are summarized.
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