Title of article :
Exposure assessment of a burning ground for chemical ammunition
on the Great War battlefields of Verdun
Author/Authors :
Tobias Bausinger، نويسنده , , ?، نويسنده , , Eric Bonnaire b، نويسنده , , Johannes Preu? a، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Abstract :
The destruction of arsenical shells from the 1914/18 war in the vicinity of Verdun (France) during the 1920s resulted in a locally
limited but severe soil contamination by arsenic and heavy metals. At the study site, themain part of the contaminant inventory occurs in
the upper 20 cm of the topsoil which is essentially composed of combustion residues. Besides, some Cu (cmax.=16,877 mg/kg) and
Pb (cmax.=26,398 mg/kg) in this layer, As (cmax.=175,907 mg/kg) and Zn (cmax.=133,237 mg/kg) were detected in very high
concentrations. The mobilities of Cu,Mn, Pb and Zn in the soil system were derived from ammonium nitrate eluates. They are strongly
influenced by the soil pH and can be described by quadratic regression curves from which threshold pH values were calculated. Below
these valuesmore than 10%of the element contentwas available asmobile species.Within the examined pHrange, this method could not
be adopted for arsenic, because the mobility of Aswas only slightly controlled by the soil pH. In the heavily contaminated topsoil, Cu and
Pb were fixed by the moderately acidic soil pH which varied from 4.8 to 5.8. No migration to the underlying horizons occurred.
A different behavior was observed for As and Zn. The calculated threshold pH of Zn was 5.5, so certain amount of this element was
transferred to the subsoil and the leachate (cmax.=350 μg/l). However, a major dispersion of Zn was prevented by a rise of the soil pH in
the carbonate-containing subsoil. Elevated concentrations of As were found in all soil horizons up to a depth of 2 m and also in the
leachate (cmax.=2377 μg/l). Contrary to Cu, Pb and Zn the mobility of As evidently was less affected by the subsoil.
Regarding organic contaminants, nitroaromatic explosives were detected only inminor concentrations in the soil (cmax.=14.7mg/kg)
and the leachate (cmax.=13.5 μg/l). No aromatic organoarsenicals were detected in the soil and the leachate samples.
The main hazard of the site is the severe arsenic contamination and the transfer of this carcinogen by leachate, surface runoff and
probably by wind. Nevertheless, some studies on the effects of the contaminant inventory on the local vegetation revealed that
ammonium nitrate elutable zinc is responsible for the spatial distribution of some tolerant plant species and not arsenic.
Previously undetected buried munitions fromthe former delaboration facility can be an other source of environmental contaminants.
This is supported by elevated concentrations of chlorate (cmax.=71 mg/l) and perchlorate (cmax.=0.8 mg/l) detected in the leachate
samples.
This is the second report about environmental contamination related to post-war ammunition destruction activities along the
1914/18 Western Front.
Keywords :
Heavy metals , Leachate sampling , Soil contamination , Arsenicals , Explosives
Journal title :
Science of the Total Environment
Journal title :
Science of the Total Environment