Assessment of internal radiation exposure to Antarctic biota due to selected natural radionuclides in terrestrial and marine environment.

The present article introduces data on natural radioactivity (40K, 230,232Th, 234,238U) in the Antarctic marine and terrestrial environment. Various biota samples were analysed due to internal exposure to 40K, 230,232Th, 234,238U. Activity concentration of 40K was the highest in both marine and terrestrial samples. Mean values of 40K activity concentration are 1340 Bq/kg and 370 Bq/kg for the marine and terrestrial samples respectively. 234U/238U ratios analysis revealed that sea waters and sea spray are the main source of the uranium in the terrestrial samples. Average 230,232Th, 234,238U activity concentrations in the Antarctic biota do not exceed 6 Bq/kg. Weighted internal dose rates are relatively low; they range from approximately 0.1 to 0.6 µGy/h. Statistically significant differences in radionuclide accumulation were discovered between the mosses and lichens. It may point to various mechanisms of the nutrient absorption from the environment by these organisms.

The study of natural and artificial radionuclides incorporation in teeth and head bones of animals lived nearby Caetité uranium mine, Brazil.

This study aimed at assessing the incorporation of radionuclides in animals in the proximity of the uranium mine in Caetité, Brazil. In 2014, samples of bovine and equine teeth and skull bones were collected and their contents of natural and artificial isotopes were assessed using nuclear spectrometry techniques. Gamma ray emission from 226,228Ra and 40K isotopes was determined using high-purity germanium (HPGe) spectrometry, 90Sr radioactivity was measured with liquid scintillation, and 234,238U, 232,230,228Th, 210Po and 239+240Pu radioactivity was assessed with alpha-spectrometry. Prior to the measurements, sample dissolutions and isotope separations were performed. Our results indicate a high 228Th isotope content in the skull bones and the teeth of animals, up to 179 Bq per kg of ash. The 226Ra and 228Ra concentrations were slightly lower. Activity concentrations of other isotopes were significantly lower or below the detection limit. We could not identify sources of technologically enhanced levels of 228Ra in the area we investigated; therefore we suggest that their origin is natural.

Transuranic isotopes and 90Sr in attic dust in the vicinity of two nuclear establishments in northern Germany.

Attic dust was chosen as the test medium in order to search for traces of man-made bone seeking alpha and beta emitters. The samples were taken from 5 houses in the community of Elbmarsch situated at the river Elbe, adjacent to the Krümmel nuclear power plant and the nuclear research center of Geesthacht. Five houses in other regions of northern Germany were taken as a control. 238Pu, (239,240)Pu, 241Am, and 244Cm were measured by alpha spectrometry after chemical separation. Additionally, 241Pu was measured by liquid scintillation spectrometry, and the fission product 90Sr was measured in a separate investigation. All nuclides except 244Cm showed activities above the detection limit in the Elbmarsch samples and an elevated mean concentration compared to the control. It can be concluded from the activity ratio 241Am/(239,240)Pu that the Elbmarsch contamination cannot be accounted for by the background levels of transuranic nuclides resulting from weapons fallout. The derived release of alpha emitters is assumed to have contributed to the induction of a leukemia cluster in children, which was observed in Elbmarsch between 1990 and 1996.