Determination of Characteristic vs Anomalous Cs/Cs Isotopic Ratios in Radioactively Contaminated Environmental Samples.

A contamination with the ubiquitous radioactive fission product Cs cannot be assigned to its source. We used environmental samples with varying contamination levels from various parts of the world to establish their characteristic Cs/Cs isotope ratios and thereby allow their distinction. The samples included biological materials from Chernobyl and Fukushima, historic ashed human lung tissue from the 1960s from Austria, and trinitite from the Trinity Test Site, USA. After chemical separation and gas reaction shifts inside a triple quadrupole ICP mass spectrometer, characteristic Cs/Cs isotope signatures (all as per March 11, 2011) were obtained for Fukushima- (∼0.35) and Chernobyl-derived (∼0.50) contaminations, in agreement with the literature for these contamination sources. Both signatures clearly distinguish from the characteristic high ratio (1.9 ± 0.2) for nuclear-weapon-produced radiocesium found in human lung tissue. Trinitite samples exhibited an unexpected, anomalous pattern by displaying a low (<0.4) and nonuniform Cs/Cs ratio. This exemplifies a Cs-rich fractionation of the plume in a nuclear explosion, where Cs is a predominant species in the fireball. The onset of Cs was delayed because of the longer half-life of its parent nuclide Xe, causing a spatial separation of gaseous Xe from condensed Cs, which is the reason for the atypical Cs/Cs fractionation in the fallout at the test site.