Southwest intrusion of 134Cs and 137Cs derived from the Fukushima Dai-ichi nuclear power plant accident in the Western North Pacific.

Enormous quantities of radionuclides were released into the ocean via both atmospheric deposition and direct release as a result of the Fukushima Dai-ichi Nuclear Power Plant (FNPP) accident. This study discusses the southward dispersion of FNPP-derived radioactive cesium (Cs) in subsurface waters. The southernmost point where we found the FNPP-derived (134)Cs (1.5-6.8 Bq m(-3)) was 18 °N, 135 °E, in September 2012. The potential density at the subsurface peaks of (134)Cs (100-500 m) and the increased water column inventories of (137)Cs between 0 and 500 m after the winter of 2011-2012 suggested that the main water mass containing FNPP-derived radioactive Cs was the North Pacific Subtropical Mode Water (NPSTMW), formed as a result of winter convection. We estimated the amount of (134)Cs in core waters of the western part of the NPSTMW to be 0.99 PBq (decay-corrected on 11 March 2011). This accounts for 9.0% of the (134)Cs released from the FNPP, with our estimation revealing that a considerable amount of FNPP-derived radioactive Cs has been transported to the subtropical region by the formation and circulation of the mode water.

Detection and temporal variation of (60)Co in the digestive glands of the common octopus, Octopus vulgaris, in the East China Sea.

(60)Co were detected in common octopus specimens collected in the East China Sea in 1996-2005. The source of (60)Co has remained unclear yet. Stable isotope analyses showed that there was no difference in stable Co concentrations between octopus samples with (60)Co and without (60)Co. This result showed that the stable Co in the digestive gland of octopus potentially did not include a trace amount of (60)Co and the source of (60)Co existed independently. Furthermore, investigations of octopus in other area and other species indicated that the origin of the source of (60)Co occurred locally in the restricted area in the East China Sea and not in the coastal area of Japan. Concentrations of (60)Co have annually decreased with shorter half-life than the physical half-life. This decrease tendency suggests that the sources of (60)Co were identical and were temporary dumped into the East China Sea as a solid waste.

Temporal variations of 90Sr and 137Cs concentrations and the 137Cs/90Sr activity ratio in marine brown algae, Undaria pinnatifida and Laminaria longissima, collected in coastal areas of Japan.

The anthropogenic radionuclides, 90Sr and 137Cs, were measured in two marine algal species, wakame seaweed (Undaria pinnatifida) and edible kelp (Laminaria longissima), collected in four coastal areas of Japan during 1998-2008. Although 90Sr and 137Cs could be detected at all sampling sites, the concentrations of 90Sr and 137Cs were at low levels and those in some samples were below the detection limit. These low concentrations and the small variation of both concentrations and the 137Cs/90Sr activity ratio indicate that the source of 90Sr and 137Cs detected in this study originated from the global fallout deposition following atmospheric nuclear-bomb tests in the past. There were no significant differences in both concentrations of 90Sr and 137Cs in wakame seaweed among three sampling sites. Although wakame seaweed is extensively distributed in southern and central Japan, it does not occur in northern areas and so edible kelp was monitored. The concentrations of 90Sr and 137Cs in edible kelp were significantly different from those in wakame seaweed in some sampling sites. These differences could be due to the difference in the concentrations of 90Sr and 137Cs in the surrounding seawater or the difference in species. The combined data with data from the previous report and the preexisting database showed that wakame seaweed incorporated 137Cs through a different pathway from that of 90Sr. The combined data also suggested that wakame seaweed responded differently to the source of 137Cs.