Determination of Characteristic vs Anomalous ¹³⁵Cs/¹³⁷Cs Isotopic Ratios in Radioactively Contaminated Environmental...

A contamination with the ubiquitous radioactive fission product ¹³⁷Cs cannot be assigned per se to its source. We used environmental samples with varying contamination levels from various parts of the world to establish their characteristic ¹³⁵Cs/¹³⁷Cs 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 ¹³⁵Cs/¹³⁷Cs 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 ¹³⁵Cs/¹³⁷Cs ratio. This exemplifies a ¹³⁷Cs-rich fractionation of the plume in a nuclear explosion, where ¹³⁷Cs is a predominant species in the fireball. The onset of ¹³⁵Cs was delayed because of the longer half-life of its parent nuclide ¹³⁵Xe, causing a spatial separation of gaseous ¹³⁵Xe from condensed ¹³⁷Cs, which is the reason for the atypical ¹³⁵Cs/¹³⁷Cs fractionation in the fallout at the test site.