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Distribution of the Fukushima-derived radionuclides in seawater in the Pacific off the coast of Miyagi, Fukushima, and Ibaraki Prefectures, Japan.

Authors :
Oikawa, S.
Takata, H.
Watabe, T.
Misonoo, J.
Kusakabe, M.
Source :
Biogeosciences Discussions; 2013, Vol. 10 Issue 3, p4851-4886, 63p, 4 Color Photographs, 1 Black and White Photograph, 9 Charts, 3 Graphs
Publication Year :
2013

Abstract

The activities of artificial radionuclides in seawater samples collected off the coast of Miyagi, Fukushima, and Ibaraki Prefectures were measured as part of a monitoring program initiated by the Japanese government Ministry of Education, Sports, Science and Technology immediately after the Fukushima Dai-ichi nuclear power plant accident. The spatial and temporal distributions of those activities are summarized herein. The activities of strontium-90, iodine-131, cesium-134 and -137 (i.e. <superscript>90</superscript>Sr, <superscript>131</superscript>I, <superscript>134</superscript>Cs, and <superscript>137</superscript>Cs) derived from the accident were detected in seawater samples taken from areas of the coastal ocean adjacent to the power plant. No <superscript>131</superscript>I was detected in surface waters (≤5m depth) or in intermediate and bottom waters after 30 April 2011. Strontium-90 was found in surface waters collected from a few sampling stations in mid-August 2011 to mid-December 2011. Temporal changes of <superscript>90</superscript>Sr activity in surface waters were evident, although the <superscript>90</superscript>Sr activity at a given time varied widely between sampling stations. The activity of <superscript>90</superscript>Sr in surface waters decreased slowly over time, and by the end of December 2011 had reached background levels recorded before the accident. Radiocesium, <superscript>134</superscript>Cs and <superscript>137</superscript>Cs, was found in seawater samples immediately after the accident. There was a remarkable change in <superscript>137</superscript>Cs activities in surface waters during the first 7 months (March through September 2011) after the accident; the activity reached a maximum in the middle of April and thereafter decreased exponentially with time. Qualitatively, the distribution patterns in surface waters suggested that in early May <superscript>137</superscript>Cs-polluted water was advected northward; some of the water then detached and was transported to the south. Two cores of the water with high <superscript>137</superscript>Cs activity persisted at least until July 2011. In subsurface waters <superscript>137</superscript>Cs activity was first detected in the beginning of April 2011, and the water masses were characterized by ςt (an indicator of density) values of 25.5-26.5. From 9-14 May to 5-16 December 2011, the depths of the water masses increased with time, an indication that deepening of the isopycnals with time can be an important mechanism for the transport of <superscript>137</superscript>Cs downward in coastal waters. During 4-21 February 2012, the water column became vertically homogeneous, probably because of convective mixing during the winter, the result being nearly constant values of <superscript>137</superscript>Cs activity throughout the water column from the surface to the bottom (~200m depth) at each station. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18106277
Volume :
10
Issue :
3
Database :
Complementary Index
Journal :
Biogeosciences Discussions
Publication Type :
Academic Journal
Accession number :
87630274
Full Text :
https://doi.org/10.5194/bgd-10-4851-2013