Highlights
- Cs-137 plume strongly diluted by July 2011, reaches American coast by 2014.
- Mode water formation and persistent upwelling affect Cs-137 concentrations.
- Cs-137 enters the deep ocean and exits the North Pacific in the next 30 years.
- Sensitivity to uncertainties in the source function and to interannual variability.
Abstract
Following
the March 2011 Fukushima disaster, large amounts of water contaminated
with radionuclides, including Cesium-137, were released into the Pacific
Ocean. With a half-life of 30.1 years, Cs-137 has the potential to
travel large distances within the ocean. Using an ensemble of regional
eddy-resolving simulations, this study investigates the long-term
ventilation pathways of the leaked Cs-137 in the North Pacific Ocean.
The simulations suggest that the contaminated plume would have been
rapidly diluted below 10,000 Bq/m3 by the energetic Kuroshio Current and Kurushio Extension by July 2011. Based on our source function of 22 Bq/m3, which sits at the upper range of the published estimates, waters with Cs-137 concentrations >10 Bq/m3
are projected to reach the northwestern American coast and the Hawaiian
archipelago by early 2014. Driven by quasi-zonal oceanic jets, shelf
waters north of 45°N experience Cs-137 levels of 10–30 Bq/m3 between 2014 and 2020, while the Californian coast is projected to see lower concentrations (10–20 Bq/m3)
slightly later (2016–2025). This late but prolonged exposure is related
to subsurface pathways of mode waters, where Cs-137 is subducted toward
the subtropics before being upwelled from deeper sources along the
southern Californian coast. The model suggests that Fukushima-derived
Cs-137 will penetrate the interior ocean and spread to other oceanic
basins over the next two decades and beyond. The sensitivity of our
results to uncertainties in the source function and to inter-annual to
multi-decadal variability is discussed.
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