Johannes Lachner

Isotopic signature of plutonium at Bikini atoll

Atom ratios of the isotopes (239)Pu, (240)Pu, (241)Pu and (244)Pu were determined in sediments and soils from Bikini atoll using low energy Accelerator Mass Spectrometry. All samples had been contaminated by local fallout from nuclear weapon testing between 1946 and 1958 and show significant variations in the isotopic composition, which are ascribed to the different yields of single tests and to the mixture of material from various devices. Differences in the (244)Pu/(239)Pu ratio (2.8-5.7x10(-4)) are more pronounced than in the (240)Pu/(239)Pu ratio of the same samples and provide complementary information to distinguish the sources of contamination.

41Ca, 14C and 10Be concentrations in coral sand from the Bikini atoll.

Activation measurements of materials exposed to nuclear bomb explosions are widely used to reconstruct the neutron flux for retrospective dosimetry. In this study the applicability of coral CaCO3 as a biogenic neutron fluence dosimeter is tested. The long-lived radioisotopes (41)Ca, (14)C and (10)Be, which had been produced in nuclear bomb explosions, are measured in several coral sand samples from the Bikini atoll at the 600 kV and 200 kV AMS facilities of ETH Zurich. Elevated concentrations of all studied isotopes are found in a sample from the crater that was initially formed by the high-yield nuclear explosion Castle Bravo in 1954 and that had been used as site for several tests afterward. The observed (14)C concentration is considered too large to originate from neutron irradiation of CaCO3 alone. The relatively low concentration of (10)Be found in the crater sample indicates that production of (10)Be during nuclear bomb testing is generally minor. A simple neutron fluence reconstruction is performed on basis of the (41)Ca/(40)Ca ratio.

Anthropogenic 236U in the North Sea – a closer look into a source region

In this study we present new seawater data of 236U and 238U sampled in the North Sea in 2010. The North Sea has been and is still receiving a considerable input of anthropogenic radionuclides from nuclear reprocessing facilities located in La Hague (France) and Sellafield (Great Britain). It therefore represents an important source region for oceanographic tracer studies using the transient signal of anthropogenic 236U. A proper knowledge of the sources of 236U is an essential prerequisite for such tracer studies. The 236U data set presented in this study covers the transition regions of the North Sea to the Atlantic Ocean, to the Baltic Sea, and upstream the Elbe River. It is discussed in the context of available 236U data from the literature. Our results show that both 236U concentrations and 236U/238U ratios in surface waters of the North Sea can be explained by simple binary mixing models implying that 236U behaves conservatively in seawater. We further show that the input of 236U by the Elbe River is negligible, while there might be a maximum input of 12 g/yr via the Baltic Sea. The results of the mixing models suggest that this still unidentified 236U contamination could be supplied by fresh water input.