Retention of 2011 Fukushima Dai-ichi NPP accident-derived 137Cs in the northern North Pacific–Bering Sea

Tracing soluble radionuclides is critical for understanding the mechanisms underlying the transport of soluble materials in marine environments. In the present study, we investigated the surface distribution of the concentrations (activities) of <sup>134</sup>Cs, <sup>137</sup>Cs, <sup>226</sup>Ra, and <sup>228</sup>Ra in the northern North Pacific, Bering Sea, and Arctic regions from 2017 to 2024. The <sup>226</sup>Ra and <sup>228</sup>Ra concentrations distinctively separated the surface into the low-<sup>226</sup>Ra subtropical-transition and high-<sup>226</sup>Ra subarctic current areas in the northern North Pacific and the <sup>228</sup>Ra-rich eastern shelf and <sup>228</sup>Ra-poor western basin areas in the Bering Sea. In 2022-2024, the surface concentrations of the Fukushima Dai-ichi Nuclear Power Plant accident-derived <sup>137</sup>Cs (FD-<sup>137</sup>Cs) ranged between 0.4 and 1.5 mBq/L, with the highest values in the eastern shelf of the Bering Sea. The lateral distribution of <sup>137</sup>Cs concentrations is predominantly ascribed to the preferential inflow of FD-<sup>137</sup>Cs to the Bering Sea along with the upstream Alaskan Coastal Current. After the steep increase from 2015 to 2017, the temporal variation in FD-<sup>137</sup>Cs concentrations in the Bering Sea was small (0.8-1.5 mBq/L from 2018 to 2024). This could be attributed to the continual transport of FD-<sup>137</sup>Cs from the Alaskan Gyre area via the Aleutian Islands.

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Publication Details

Journal
Scientific Reports
Published
2025-10-17
DOI
https://doi.org/10.1038/s41598-025-20520-w
Primary Topic
Radioactive contamination and transfer
Type
article
Field-Weighted Citation Impact
0.00

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article

Retention of 2011 Fukushima Dai-ichi NPP accident-derived 137Cs in the northern North Pacific–Bering Sea

Yuichiro Kumamoto, Daïki Nomura, Seiya Nagao, Hayata Mitsunushi et al.
Scientific Reports
Radioactive contamination and transfer
article

Retention of 2011 Fukushima Dai-ichi NPP accident-derived 137Cs in the northern North Pacific–Bering Sea

Yuichiro Kumamoto, Daïki Nomura, Seiya Nagao, Hayata Mitsunushi, Mutsuo Inoue, Yasunori Hamajima, Daichi Koshiishi
article en

Abstract

Tracing soluble radionuclides is critical for understanding the mechanisms underlying the transport of soluble materials in marine environments. In the present study, we investigated the surface distribution of the concentrations (activities) of <sup>134</sup>Cs, <sup>137</sup>Cs, <sup>226</sup>Ra, and <sup>228</sup>Ra in the northern North Pacific, Bering Sea, and Arctic regions from 2017 to 2024. The <sup>226</sup>Ra and <sup>228</sup>Ra concentrations distinctively separated the surface into the low-<sup>226</sup>Ra subtropical-transition and high-<sup>226</sup>Ra subarctic current areas in the northern North Pacific and the <sup>228</sup>Ra-rich eastern shelf and <sup>228</sup>Ra-poor western basin areas in the Bering Sea. In 2022-2024, the surface concentrations of the Fukushima Dai-ichi Nuclear Power Plant accident-derived <sup>137</sup>Cs (FD-<sup>137</sup>Cs) ranged between 0.4 and 1.5 mBq/L, with the highest values in the eastern shelf of the Bering Sea. The lateral distribution of <sup>137</sup>Cs concentrations is predominantly ascribed to the preferential inflow of FD-<sup>137</sup>Cs to the Bering Sea along with the upstream Alaskan Coastal Current. After the steep increase from 2015 to 2017, the temporal variation in FD-<sup>137</sup>Cs concentrations in the Bering Sea was small (0.8-1.5 mBq/L from 2018 to 2024). This could be attributed to the continual transport of FD-<sup>137</sup>Cs from the Alaskan Gyre area via the Aleutian Islands.

Scientific ReportsVol. 15(1)
Kanazawa University (JP), Japan Agency for Marine-Earth Science and Technology (JP), Hokkaido University (JP)
Institute of Nature and Environmental Technology, Kanazawa University, Kanazawa University, Japan Society for the Promotion of Science, JST-Mirai Program
Openalex Percentile: Top 73%
Radioactive contamination and transfer
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