Abstract
The environmental dynamics of Fukushima-derived radiocaesium from land to ocean and the impact of its flux on the marine environment are matters of concern because radiocaesium will be continually transported to the open ocean for the next several decades, or possibly more than one hundred years. In order to assess the distribution and flux of radiocaesium in a river-estuary-ocean system, we investigated the activity concentration of radiocaesium in Matsukawa-ura Lagoon, the largest lagoon in Fukushima, where it is very easy to carry out observations with a wide salinity gradient. Activity concentrations of dissolved 137Cs are elevated in seawater of low to intermediate salinity. It can thus be inferred that radiocaesium desorbs from suspended particles in an estuarine area. The porewater activity concentration of 137Cs in lagoon sediment was about 10 times higher than that in the overlying lagoon water. This direct measurement indicates that a significant amount of radiocaesium in sediment desorbs into porewater. From the results of a mass balance model, dissolved 137Cs flux from the lagoon's bottom is 15.3 ± 3.7 times greater than the riverine input, including desorption from particles. In the case of the whole Pacific coast of northeastern Japan (Miyagi, Fukushima, and Ibaraki Prefectures), dissolved 137Cs flux into the open ocean, including diffusion of porewater, is estimated to be up to 1.5 times greater than the sum of riverine input and the ongoing release from the Fukushima Dai-ichi Nuclear Power Station's harbor. Consequently, our results suggest that radiocaesium is transported to the open ocean under the control of various processes, not only by desorption from particles but also, for example, by the diffusion of porewater.
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