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Kilder til BAM-forurening og forureningsudbredelse
The pesticide (or pesticide degradation product) which has hitherto polluted most water
extraction wells in Denmark is 2.6-dichlorbenzamide (BAM). BAM derives from the herbicides
Prefix and Casoron and is a degradation product of the active substances dichlobenil and
chlorthiamide in these herbicides. The herbicide products were used in the period from
1965 to 1997 but are now prohibited.
The average annual consumption in Denmark of chlorthiamid and dichlobenil was 29,000
kg/year in the period 1965-1997. The application dose of dichlobenil was around 4-30 kg
active substance per ha.
Prefix and Casoron were used widely by many different users in different areas (not in
order of priorities):
 | Courtyards for farm holdings |
 | Gardening/market gardens (in greenhouses, courtyards and surrounding areas) |
 | Plantations (under bushes and trees in fruit- and spruce plantations and on the
courtyard) |
 | Nursery gardens (in beds and walks) |
 | Allotments and kitchen gardens (in beds and walks) |
 | Apartments blocks (in beds, walks, parking areas, playgrounds) |
 | Single-family houses (in beds, walks and driveways) |
 | Parks/recreational areas (in beds, walks and playgrounds) |
 | Churchyards (walks) |
 | Sport grounds (walks, running tracks, tennis courts etc.) |
 | Schools and child-care institutions (beds, walks, playgrounds) |
 | Public buildings/hospitals etc. (beds, walks, parking areas) |
 | Roads (road verges, sidewalks, footpaths) |
 | Railroads/railroad stations |
 | Waterwork sites (non-paved areas) |
 | Surrounding areas around waterwork wells |
Weed control using Casoron and Prefix occurred both in urban and agricultural
groundwater catchment areas. The number of BAM contaminant sources, however, is typically
much higher in urban areas and the contaminant sources closer compared to agricultural
areas.
Investigations of the BAM contaminant sources show concentrations of typically up to
100 µg/kg of the parent pesticide dichlobenil in soils. The average concentration in the
top 1 meter is at approx. 55 µg/kg. Dichlobenil is found in soil samples in more than
half of the investigated sites, regardless of knowledge of dichlobenil-containing
herbicides having been used at the sites or not. It is assumed that the herbicides have
not been used since 1997, and that the observed concentrations of dichlobenil represent
residual concentrations of dichlobenil that has not been degraded. Small amounts of BAM is
also detected in the soil, which shows that dichlobenil is still degraded and that BAM
continues to infiltrate from the surface. BAM is also detected in pore-water from vadose
zone (in concentrations of up to 37 µg/l) as well in groundwater aquifers near the ground
surface, which shows that BAM is still leaching through vadose zone to the groundwater.
Often, 2.6-dichlorobenzoic acid also is detected in pore water samples from the vadose
zone, indicating that BAM is degraded since 2.6-dichlorobenzoic acid in the literature is
reported as being a metabolite from BAM.
Calculations show that the residuals of dichlobenil in soils from the upper few meters
of the investigated sites can still cause groundwater contamination for many years to
come. However, the main part of BAM is considered to have already infiltrated into deeper
parts of vadose zone or into the groundwater aquifer.
Apart from the direct infiltration of BAM from the contaminant sources there might be a
risk of spreading BAM via surface water (streams) and rainwater runoff from roads and
paved surfaces. For instance, rainwater basins without firm bottom imply a risk of
infiltration into the groundwater of BAM polluted rainwater.
Investigations of selected groundwater catchments have shown that the many BAM
contaminant sources in urban and agricultural areas have caused widely spreaded
BAM-pollution in the groundwater aquifers. The spreading of BAM-pollution is caused by
leaching of BAM from all these contaminant sources resulting in many small pollution
plumes which often seem to combine to larger coherent plumes due to the high mobility of
BAM. The complex distribution of contaminant sources in the catchment areas combined with
the spreading of BAM via surface water and runoff rainwater pattern makes it very
difficult to identify preferential pathways from the contaminant source to the
groundwater.
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