Chenery, S.R.N.; Ander, E.L.; Perkins, K.M.; Smith, B.. 2002 Uranium anomalies identified using G-BASE data - natural or anthropogenic? A uranium isotope pilot study. Nottingham, UK, British Geological Survey, 34pp. (IR/02/001) (Unpublished)
Abstract
The rapid quantitative analysis by inductively coupled plasma quadrupole mass spectrometry
(ICP-QMS) for uranium isotope ratios has been successfully established and tested. The method
is fully documented in this report.
The rapid and cost effective nature of the methodology has allowed the analysis of a selection of
G-BASE soil and stream sediment archive material to be undertaken, which was not possible
previously. These samples were chosen by careful consideration of the findings of previously
published G-BASE atlases. During the course of mapping Britain, the G-BASE project has
encountered anomalously high concentrations of uranium in several areas, in comparison to the
regional background values. Samples from regions believed to be enhanced in uranium due to
natural processes alone were chosen to allow the variability of uranium isotope ratios to be
quantified, and hence provide an isotopic baseline. Samples which had been recognised during
geochemical baseline mapping as having anomalously high uranium concentrations in the locale
of nuclear fuel installations were also selected for comparison with this isotopic baseline.
As would be expected from literature values, the 238/235U ratio was constant in all the natural
enhanced samples, whilst some variation in 238/234U was observed. This was also the case for
samples from the urban industrial fringes of Greater Merseyside, which had high concentrations
of heavy metal contaminants. In contrast, all samples associated, by proximity, with nuclear fuel
facilities were found to have isotope ratios reflecting a contribution from enriched uranium.
These results are consistent with the limited suite of RIFE (Radioactivity in Food and the
Environment) data available, but are of better precision.
Difficulties exist in quantifying the contribution of processing facility uranium to stream
sediments and soils, due to the limited information available on the likely composition of the
original materials entering the stream course, or soil profile. These factors are highlighted, along
with possible further investigations to elucidate dissemination of anthropogenic uranium in the
environment.
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