标题：Temporal variations of 90 Sr and 137 Cs in atmospheric depositions after the Fukushima Daiichi Nuclear Power Plant accident with long-term observations
摘要：We have measured artificial radionuclides, such as 90Sr and 137Cs, in atmospheric depositions since 1957 in Japan. We observed the variations in 90Sr and 137Cs, which were emitted from atmospheric nuclear tests and nuclear power plant accidents, due to their diffusion, deposition, and resuspension. In March 2011, the Fukushima Daiichi Nuclear Power Plant accident occurred in Japan, and significant increases in 90Sr and 137Cs were detected at our main site in Tsukuba, Ibaraki. Our continual observations revealed that the 137Cs monthly deposition rate in 2018 declined to ~ 1/8100 of the peak level, but it remained more than ~ 400 times higher than that before the accident. Chemical analysis suggested that dust particles were the major carriers of 90Sr and 137Cs during the resuspension period at our main site. Presently, the effective half-life for 137Cs deposition due to radioactive decay and other environmental factors is 4.7 years. The estimation suggests that approximately 42 years from 2011 are required to reduce the atmospheric 137Cs deposition to a state similar to that before the accident. The current 90Sr deposition, on the other hand, shows the preaccident seasonal variation, and it has returned to the same radioactive level as that before the accident.
其他摘要：Abstract We have measured artificial radionuclides, such as 90 Sr and 137 Cs, in atmospheric depositions since 1957 in Japan. We observed the variations in 90 Sr and 137 Cs, which were emitted from atmospheric nuclear tests and nuclear power plant accidents, due to their diffusion, deposition, and resuspension. In March 2011, the Fukushima Daiichi Nuclear Power Plant accident occurred in Japan, and significant increases in 90 Sr and 137 Cs were detected at our main site in Tsukuba, Ibaraki. Our continual observations revealed that the 137 Cs monthly deposition rate in 2018 declined to ~ 1/8100 of the peak level, but it remained more than ~ 400 times higher than that before the accident. Chemical analysis suggested that dust particles were the major carriers of 90 Sr and 137 Cs during the resuspension period at our main site. Presently, the effective half-life for 137 Cs deposition due to radioactive decay and other environmental factors is 4.7 years. The estimation suggests that approximately 42 years from 2011 are required to reduce the atmospheric 137 Cs deposition to a state similar to that before the accident. The current 90 Sr deposition, on the other hand, shows the preaccident seasonal variation, and it has returned to the same radioactive level as that before the accident.
