Evaluating the transport of surface seawater from 1956 to 2021 using 137Cs deposited in the global ocean as a chemical tracer

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Abstract
We analyzed the spatiotemporal variations in the 137Cs activity concentrations in global ocean surface seawater from 1956 to 2021 using the HAMGlobal2021 (Historical Artificial radioactivity database in Marine environment, Global integrated version 2021) and other published data. The global ocean was divided into 37 boxes. When observing the 0.5-year median value of 137Cs in each box in the Pacific Ocean, we noticed that the values gradually increased or had almost constant levels in the 1950s and 1960s, and then decreased exponentially in 1970–2010, immediately before the Fukushima Daiichi Nuclear Power Plant Station (F1NPS) accident. In the northern North Atlantic Ocean and its marginal sea, the 0.5-year median values of 137Cs showed large variations in the directly discharged 137Cs from the reprocessing plants. The 137Cs inventory in the surface mixed layer in 1970, when 137Cs was released into the surface seawater, was estimated to be 184±26 PBq. In 1975 and 1980, the 137Cs inventory increased to 201±27 and 214±11 PBq, respectively, due to direct discharge from the Sellafield and La Hague nuclear fuel reprocessing plants. In 2011, the 137Cs inventory in the global ocean mixed layer increased to 50.7±7.3 PBq compared to that before the F1NPS accident, in which the contribution from the accident was estimated to be approximately 15.5±3.9 PBq. Mass balance analysis indicates that 137Cs deposited by the global fallout in the western North Pacific Ocean moved to the eastern North Pacific Ocean. Subsequently, 137Cs was transported southwards, followed by westward transport in the subtropical and equatorial Pacific Ocean, and then inflowed into the Indian Ocean via the Indonesian Archipelago. The longer apparent half-residence times in the Indonesian Archipelago (36.7 years from 1973 to 1997) and central Atlantic Ocean (38.0 years from 1992 to 2016) also support the interpretation of the global-scale transport of 137Cs from the western North Pacific Ocean to the Indian (20–30 years) and Atlantic oceans (30–40 years). In the northern North Atlantic Ocean and its marginal sea, 137Cs discharged from nuclear reprocessing plants is transported to the North Sea, Barents Sea and coast of Norway, and Arctic Ocean on a decadal scale. The dataset is available at https://doi.org/10.34355/CRiED.U.Tsukuba.00085 (Aoyama, 2021), https://doi.org/10.34355/Ki-net.KANAZAWA-U.00149 (Inomata and Aoyama, 2022a), https://doi.org/10.34355/Ki-net.KANAZAWA-U.00150 (Inomata and Aoyama, 2022b), and https://doi.org/10.34355/Ki-net.KANAZAWA-U.00151 (Inomata and Aoyama, 2022c).
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Funding Information
  • Ministry of Education, Culture, Sports, Science and Technology (25110511)
  • Institute of Nature and Environmental Technology, Kanazawa University (18009, 19022, 20043)

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