Impact of Fukushima-derived radiocesium in the western North Pacific Ocean about ten months after the Fukushima Dai-ichi nuclear power plant accident
- 1. Research and Development Center for Global Change, Japan Agency for Marine-Earth Science and Technology, 2-15 Natushima-cho, Yokosuka, Kanagawa 237-0061 (Japan)
- 2. Institute of Environmental Radioactivity, Fukushima University, 1-1 Kanayagawa, Fukushima 960-1296 (Japan)
- 3. Low Level Radioactivity Laboratory, Kanazawa University, Wake, Nomi, Ishikawa 923-1224 (Japan)
Description
We measured vertical distributions of radiocesium (134Cs and 137Cs) at stations along the 149°E meridian in the western North Pacific during winter 2012, about ten months after the Fukushima Dai-ichi Nuclear Power Plant (FNPP1) accident. The Fukushima-derived 134Cs activity concentration and water-column inventory were largest in the transition region between 35 and 40°N approximately due to the directed discharge of the contaminated water from the FNPP1. The bomb-derived 137Cs activity concentration just before the FNPP1 accident was derived from the excess 137Cs activity concentration relative to the 134Cs activity concentration. The water-column inventory of the bomb-derived 137Cs was largest in the subtropical region south of 35°N, which implies that the Fukushima-derived 134Cs will also be transported from the transition region to the subtropical region in the coming decades. Mean values of the water-column inventories decay-corrected for the Fukushima-derived 134Cs and the bomb-derived 137Cs were estimated to be 1020 ± 80 and 820 ± 120 Bq m−2, respectively, suggesting that in winter 2012 the impact of the FNPP1 accident in the western North Pacific Ocean was nearly the same as that of nuclear weapons testing. Relationship between the water-column inventory and the activity concentration in surface water for the radiocesium is essential information for future evaluation of the total amount of Fukushima-derived radiocesium released into the North Pacific Ocean. - Highlights: • Fukushima-derived 134Cs inventory were largest in the transition region. • Bomb-derived 137Cs just before the Fukushima accident was determined. • Bomb-derived 137Cs inventory was largest in the subtropical region. • Fukushima-derived 134Cs and bomb-derived 137Cs were nearly equivalent in winter 2012
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jenvrad.2014.11.010Additional details
Identifiers
- DOI
- 10.1016/j.jenvrad.2014.11.010;
- PII
- S0265-931X(14)00344-0;
Publishing Information
- Journal Title
- Journal of Environmental Radioactivity
- Journal Volume
- 140
- Journal Page Range
- p. 114-122
- ISSN
- 0265-931X
- CODEN
- JERAEE
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47010962
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ABUNDANCE; CESIUM 134; CESIUM 137; DISTRIBUTION; ECOLOGICAL CONCENTRATION; FUKUSHIMA DAIICHI NUCLEAR POWER STATION; NUCLEAR DECAY; PACIFIC OCEAN; RADIATION MONITORING; RADIONUCLIDE MIGRATION; REACTOR ACCIDENTS; SEAWATER; SURFACES
- Descriptors DEC
- ACCIDENTS; BETA DECAY RADIOISOTOPES; BETA-MINUS DECAY RADIOISOTOPES; CESIUM ISOTOPES; DECAY; ELECTRON CAPTURE RADIOISOTOPES; ENVIRONMENTAL TRANSPORT; HOURS LIVING RADIOISOTOPES; HYDROGEN COMPOUNDS; INTERMEDIATE MASS NUCLEI; INTERNAL CONVERSION RADIOISOTOPES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; MASS TRANSFER; MONITORING; NUCLEI; ODD-EVEN NUCLEI; ODD-ODD NUCLEI; OXYGEN COMPOUNDS; RADIOISOTOPES; REACTOR SITES; SEAS; SURFACE WATERS; WATER; YEARS LIVING RADIOISOTOPES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.