Radiocesium concentration ratios and radiation dose to wild rodents in Fukushima Prefecture

Radiocesium was dispersed from the Fukushima Dai-ichi disaster in March 2011, causing comparatively high radioactive contamination in nearby environments. Radionuclide concentrations in wild rodents (Apodemus argenteus, and Apodemus speciosus) within these areas were monitored from 2012 to 2016. However, whole-organism to soil transfer parameters (i.e., concentration ratio, CRwo-soil) for wild rodents at Fukushima were not determined and hence were lacking from the international transfer databases. We augmented the 2012–2016 data by collecting soil activity concentrations (Bq kg−1, dry mass) from five rodent sampling sites in Fukushima Prefecture, and developed corresponding CRwo-soil values for radiocesium (134Cs and 137Cs) based on rodent radioactivity concentrations (Bq kg−1, fresh mass). The CRwo-soil were added to the Wildlife Transfer Database (WTD; http://www.wildlifetransferdatabase.org/), supporting the development of the International Commission on Radiological Protection's (ICRP) environmental protection framework, and increasing the WTD from 84 to 477 entries for cesium and Muridae (‘Reference Rat’). Significant variation occurred in CRwo-soil values between study sites within Fukushima Prefecture. The geometric mean CRwo-soil, in this paper, was higher than that reported for Muridae species for Chernobyl. Radiocaesium absorbed dose rates were also estimated for wild rodents inhabiting the five Fukushima study sites and ranged from 1.3 to 33 μGy h−1. Absorbed dose rates decreased by a factor of two from 2012 to 2016. Dose rates in highly contaminated areas were within the ICRP derived consideration reference level for Reference Rat (0.1–1 mGy d−1), suggesting the possible occurrence of deleterious effects and need for radiological effect studies in the Fukushima area

Direct Quantification of Attogram Levels of Strontium-90 in Microscale Biosamples Using Isotope Dilution-Thermal Ionization Mass Spectrometry Assisted by Quadrupole Energy Filtering

Although thermal ionization mass spectrometry (TIMS) has been employed for the high-precision analysis of isotope ratios, direct quantification of artificial mono-nuclide in the environment is difficult by even using isotope dilution (ID) due to the coexistence of the great magnitude of natural stable nuclides or isobars. In traditional TIMS and ID-TIMS, a sufficient amount of stable Sr doped on a filament is required to realize a stable and adequate ion-beam intensity (i.e., thermally ionized beams). However, the background noise (BGN) at m/z 90, detected by an electron multiplier, disturbs 90Sr analysis at low concentration levels due to peak tailing of a significant 88Sr ion beam dependent on the 88Sr-doping amount. Here, TIMS assisted by quadruple energy filtering was successfully employed for the direct quantification of attogram levels of an artificial monoisotopic radionuclide strontium-90 (90Sr) in microscale biosamples. Direct quantification was achieved by integrating the ID quantification of natural Sr and simultaneous 90Sr/86Sr isotope ratio analysis. Additionally, the measurement amount calculated by the combination of the ID and intercalibration was corrected for the net result amount of 90Sr by subtracting dark noise and the detected amount derived from the survived 88Sr, which are equivalent with the BGN intensity at m/z 90. Background correction revealed that the detection limits were in the range of 6.15 × 10–2–3.90 × 10–1 ag (0.31–1.95 μBq), depending on the concentration of natural Sr in a 1 μL sample, and the quantification of 0.98 ag (5.0 μBq) of 90Sr in 0–300 mg/L of natural Sr was successful. This method could analyze small sample quantities (1 μL), and the quantitative results were verified against authorized radiometric analysis techniques. Furthermore, the amount of 90Sr in actual teeth was successfully quantified. This method will be a powerful tool for measuring 90Sr in the measurement of micro-samples, which are required to assess and understand the degree of internal radiation exposure

Evaluation of DNA damage and stress in wildlife chronically exposed to low-dose, low-dose rate radiation from the Fukushima Dai-ichi Nuclear Power Plant accident

The health effects associated with chronic low-dose, low-dose rate (LD-LDR) exposures to environmental radiation are uncertain. All dose-effect studies conducted outside controlled laboratory conditions are challenged by inherent complexities of ecological systems and difficulties quantifying dose to free-ranging organisms in natural environments. Consequently, the effects of chronic LD-LDR radiation exposures on wildlife health remain poorly understood and much debated. Here, samples from wild boar (Sus scrofa leucomystax) and rat snakes (Elaphe spp.) were collected between 2016 and 2018 across a gradient of radiation exposures in Fukushima, Japan. In vivo biomarkers of DNA damage and stress were evaluated as a function of multiple measurements of radiation dose. Specifically, we assessed frequencies of dicentric chromosomes (Telomere-Centromere Fluorescence in situ Hybridization: TC-FISH), telomere length (Telo-FISH, qPCR), and cortisol hormone levels (Enzyme Immunoassay: EIA) in wild boar, and telomere length (qPCR) in snakes. These biological parameters were then correlated to robust calculations of radiation dose rate at the time of capture and plausible upper bound lifetime dose, both of which incorporated internal and external dose. No significant relationships were observed between dicentric chromosome frequencies or telomere length and dose rate at capture or lifetime dose (p value range: 0.20–0.97). Radiation exposure significantly associated only with cortisol, where lower concentrations were associated with higher dose rates (r2 = 0.58; p < 0.0001), a relationship that was likely due to other (unmeasured) factors. Our results suggest that wild boar and snakes chronically exposed to LD-LDR radiation sufficient to prohibit human occupancy were not experiencing significant adverse health effects as assessed by biomarkers of DNA damage and stress