Effect of intense rainfall on the distribution of Fukushima-accident-derived (137)Cs in soil was examined. Inventories and vertical distributions of (137)Cs in soils were determined at 15 locations (including croplands, grasslands, and forests) in Fukushima city in the post-rainy season, approximately 4.5months after the accident, and were compared with those in the pre-rainy season determined in our former study. The (137)Cs inventory levels scarcely changed between points in time spanning the first rainy season after the accident. Moreover, the majority of (137)Cs remained stored in the aboveground vegetation and in the upper 5cm of soil layer at undisturbed locations in the post-rainy season. A more quantitative analysis with the characterization of the vertical profile of (137)Cs using the relaxation length confirmed that the vertical profile was almost unchanged at most locations. Accordingly, it is concluded that rainfall during the rainy season had a limited effect on (137)Cs distribution in the soil, indicating the very low mobility. Chemical extraction of (137)Cs from selected soil samples indicated that (137)Cs in the soil was barely water soluble, and even the fraction extracted with 1M ammonium acetate was only approximately 10%. This further supports the low mobility of (137)Cs in our soils. Soil mineralogical analyses, which included the identification of clay minerals, suggested that smectite and mica could lower the exchangeable fraction of (137)Cs. However, no direct relationship was obtained between mineral composition and (137)Cs retention in the upper soil layer. In contrast, positive correlations were observed between (137)Cs extractability and soil properties such as pH, organic matter content, finer-sized particle content, and cation-exchange capacity. These results suggest that the mineralogical effect on the firm fixation of (137)Cs on soil constituents may be masked by the non-specific adsorption offered by the physicochemical properties of the soils.
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http://dx.doi.org/10.1016/j.scitotenv.2012.12.087 | DOI Listing |
J Environ Radioact
January 2025
Institute of Nature and Environmental Technology, Kanazawa University, Kakuma, 920-1192, Kanazawa, Ishikawa, Japan.
Radionuclides, including I, were released into the atmosphere by the Fukushima nuclear power plant accident. We measured the dissolved I concentration in 11 rivers in eastern Fukushima from 2016 to 2020 to clarify the I concentration level in river water under base-flow conditions. During the study period, the maximum I concentration in the river water was 1.
View Article and Find Full Text PDFJ Environ Radioact
January 2025
Hama Agricultural Regeneration Research Centre, Fukushima Agricultural Technology Center, Minami-soma, Fukushima, 975-0036, Japan.
Radioactive cesium released into the atmosphere caused by the Fukushima Dai-ichi Nuclear Power Plant accident in March 2011 has contaminated the surrounding area. We confirmed the applicability of in-situ methods to evaluate the depth distribution of Cs by employing the ratio of Compton-scattering and photo-peak components (r) obtained from measured gamma-ray spectra. In the present study, we applied the in-situ method to farmlands in Fukushima Prefecture whose sites were disturbed by decontamination and plowing operations.
View Article and Find Full Text PDFJ Environ Radioact
January 2025
Savannah River Ecology Laboratory, Warnell School of Forestry and Natural Resources, University of Georgia, Aiken, SC, USA.
The primary aim of this study was to quantify patterns in the distribution of Sr and Cs activity in pine (Pinus sylvestris L.: 18 sites) and birch (Betula pendula Roth.: 2 sites) forests within the Chornobyl exclusion zone, 30 years after the Chornobyl nuclear power plant (NPP) accident (1986).
View Article and Find Full Text PDFJ Environ Radioact
January 2025
Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PSE-ENV/STAAR/LRTA, PSE-ENV/SPDR/LT2S, Saint-Paul-lez-Durance, F-13115, France. Electronic address:
The transfer of radionuclides discharged into rivers by nuclear facilities are conditioned by their solid/liquid fractionation, commonly represented by an equilibrium approach using the distribution coefficient K. This coefficient, largely used in modeling, assumes an instantaneous and completely reversible reaction. However, such assumptions are rarely verified.
View Article and Find Full Text PDFSensors (Basel)
December 2024
Freiburg Materials Research Center, Albert-Ludwigs-Universität Freiburg, 79104 Freiburg im Breisgau, Germany.
Nuclear power plant decommissioning requires the rapid and accurate classification of radioactive waste in narrow spaces and under time constraints. Photon-counting detector technology offers an effective solution for the quick classification and detection of radioactive hotspots in a decommissioning environment. This paper characterizes a 5 mm CdTe Timepix3 detector and evaluates its feasibility as a single-layer Compton camera.
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