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Post-deposition early-phase migration and retention behavior of radiocesium in a litter–mineral soil system in a Japanese deciduous forest affected by the Fukushima nuclear accident.

Authors :
Koarashi, Jun
Nishimura, Syusaku
Nakanishi, Takahiro
Atarashi-Andoh, Mariko
Takeuchi, Erina
Muto, Kotomi
Source :
Chemosphere. Dec2016, Vol. 165, p335-341. 7p.
Publication Year :
2016

Abstract

The fate of radiocesium ( 137 Cs) derived from the Fukushima nuclear accident and associated radiation risks are largely dependent on its migration and retention behavior in the litter–soil system of Japanese forest ecosystems. However, this behavior has not been well quantified. We established field lysimeters in a Japanese deciduous broad-leaved forest soon after the Fukushima nuclear accident to continuously monitor the downward transfer of 137 Cs at three depths: the litter–mineral soil boundary and depths of 5 cm and 10 cm in the mineral soil. Observations were conducted at two sites within the forest from May 2011 to May 2015. Results revealed similar temporal and depth-wise variations in 137 Cs downward fluxes for both sites. The 137 Cs downward fluxes generally decreased year by year at all depths, indicating that 137 Cs was rapidly leached from the forest-floor litter layer and was then immobilized in the upper (0–5 cm) mineral soil layer through its interaction with clay minerals. The 137 Cs fluxes also showed seasonal variation, which was in accordance with variations in the throughfall and soil temperature at the sites. There was no detectable 137 Cs flux at a depth of 10 cm in the mineral soil in the third and fourth years after the accident. The decreased inventory of mobile (or bioavailable) 137 Cs observed during early stages after deposition indicates that the litter–soil system in the Japanese deciduous forest provides only a temporary source for 137 Cs recycling in plants. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
165
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
118542994
Full Text :
https://doi.org/10.1016/j.chemosphere.2016.09.043