Abstract

This study investigated the transport of 137Cs within a forest ecosystem by examining temporal changes in the inventory and determining the major pathways of transfer following significant atmospheric deposition. A forested area of eastern Japan was monitored for four years immediately after the Fukushima nuclear power plant accident in March 2011 that released a large amount of radionuclides. The long physical half-life of 137Cs means that contamination can persist for decades, so it is vital to understand the mechanisms underlying the 137Cs dynamics in ecosystems. We sampled litterfall, throughfall, and soil, mainly from a cedar stand, over a four-year period, and analyzed the 137Cs concentrations of each sample to determine the transfer rate and total inventory. After validating our methodology through a comparison with results from an earlier study, we determined the temporal changes in the 137Cs distribution and in the major transfer pathway. Results showed that most 137Cs intercepted by canopies was transferred rapidly over the first nine months, and that the major pathway was not litterfall but throughfall. The ecological half-life of the 137Cs stocked in the canopy was calculated for both the early and later stages of contamination. Although the former is consistent with previous results, the latter ecological half-life is somewhat longer, probably because of dependence on the meteorological and tree physiological conditions at the site. This study presents valuable new data on the post-Fukushima 137Cs contamination, enhancing our understanding of the associated dynamics in forest ecosystems.

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