Regression model analysis of the decreasing trend of cesium-137 concentration in the atmosphere since the Fukushima accident.

The decreasing trend of the atmospheric 137Cs concentration in two cities in Fukushima prefecture was analyzed by a regression model to clarify the relation between the parameter of the decrease in the model and the trend and to compare the trend with that after the Chernobyl accident. The 137Cs particle concentration measurements were conducted in urban Fukushima and rural Date sites from September 2012 to June 2015. The 137Cs particle concentrations were separated in two groups: particles of more than 1.1 µm aerodynamic diameters (coarse particles) and particles with aerodynamic diameter lower than 1.1 µm (fine particles). The averages of the measured concentrations were 0.1 mBq m-3 in Fukushima and Date sites. The measured concentrations were applied in the regression model which decomposed them into two components: trend and seasonal variation. The trend concentration included the parameters for the constant and the exponential decrease. The parameter for the constant was slightly different between the Fukushima and Date sites. The parameter for the exponential decrease was similar for all the cases, and much higher than the value of the physical radioactive decay except for the concentration in the fine particles at the Date site. The annual decreasing rates of the 137Cs concentration evaluated by the trend concentration ranged from 44 to 53% y-1 with average and standard deviation of 49 ± 8% y-1 for all the cases in 2013. In the other years, the decreasing rates also varied slightly for all cases. These indicated that the decreasing trend of the 137Cs concentration was nearly unchanged for the location and ground contamination level in the three years after the accident. The 137Cs activity per aerosol particle mass also decreased with the same trend as the 137Cs concentration in the atmosphere. The results indicated that the decreasing trend of the atmospheric 137Cs concentration was related with the reduction of the 137Cs concentration in resuspended particles.

Radiocarbon Concentrations in Environmental Samples Collected Near the Spent Nuclear Fuel Reprocessing Plant at Rokkasho, Aomori, Japan, During Test Operation Using Spent Nuclear Fuel.

The contribution of atmospheric discharged C to local C concentrations was investigated by analysis of C in environmental samples collected around the spent nuclear fuel reprocessing plant in Rokkasho, Aomori, Japan. From June 2006 to October 2011, the range of monthly averaged specific activities in atmospheric CO2 collected 2.6 km from the plant was 0.226-0.279 Bq g C; at several sampling times, the observed concentrations were higher than the background value. Specific activities of atmospheric C simulated with an atmospheric dispersion model coupled with a mesoscale weather model reproduced the measured values fairly well, supporting the idea that the higher measured specific activities were due to C discharged from the reprocessing plant. For investigation of the C distribution around the facility, samples of Cyperus microiria, wild annual sedge, were collected from nine locations. Plant samples collected east and west of the facility in 2008 showed slightly higher specific activities than samples collected at the other locations, reflecting the prevailing wind direction. The measured C specific activities in vegetable, polished rice, pasture, and milk samples collected around the facility did not differ significantly from the background value (except for one polished rice sample, which had a value slightly higher than background). The annual committed effective radiation dose to humans resulting from consumption of the polished rice was estimated as 3.6 × 10 mSv, which is negligibly small compared with 1 mSv, an index of the dose limit for the general public.

Tritium concentrations in the atmospheric environment at Rokkasho, Japan before the final testing of the spent nuclear fuel reprocessing plant.

This study aimed at obtaining background tritium concentrations in precipitation and air at Rokkasho where the first commercial spent nuclear fuel reprocessing plant in Japan has been under construction. Tritium concentration in monthly precipitation during fiscal years 2001-2005 had a seasonal variation pattern which was high in spring and low in summer. The tritium concentration was higher than that observed at Chiba City as a whole. The seasonal peak concentration at Rokkasho was generally higher than that at Chiba City, while the baseline concentrations of both were similar. The reason for the difference may be the effect of air mass from the Asian continent which is considered to have high tritium concentration. Atmospheric tritium was operationally separated into HTO, HT and hydrocarbon (CH(3)T) fractions, and the samples collected every 3 d-14 d during fiscal year 2005 were analyzed for these fractions. The HTO concentration as radioactivity in water correlated well with that in the precipitation samples. The HT concentration was the highest among the chemical forms analyzed, followed by the HTO and CH(3)T concentrations. The HT and CH(3)T concentrations did not have clear seasonal variation patterns. The HT concentration followed the decline previously reported by Mason and Östlund with an apparent half-life of 4.8 y. The apparent and environmental half-lives of CH(3)T were estimated as 9.2 y and 36.5 y, respectively, by combining the present data with literature data. The Intergovernmental Panel on Climate Change used the atmospheric lifetime of 12 y for CH(4) to estimate global warming in its 2007 report. The longer environmental half-life of CH(3)T suggested its supply from other sources than past nuclear weapon testing in the atmosphere.