Tropical Cyclone Ship Avoidance Program (TCSAP) for the Western North Pacific Ocean.

Abstract. Aerosol, rainwater, and sea fog water samples were collected during the cruise conducted over the subarctic western North Pacific Ocean in the summer of 2008, in order to estimate dry, wet, and sea fog deposition fluxes of atmospheric inorganic nitrogen (N). During sea fog events, mean number densities of particles with diameters larger than 0.5 μm decreased by 12–78%, suggesting that particles with diameters larger than 0.5 μm could act preferentially as condensation nuclei (CN) for sea fog droplets. Mean concentrations of nitrate (NO3−), methanesulfonic acid (MSA), and non sea-salt sulfate (nss-SO42−) in sea fog water were higher than those in rainwater, whereas those of ammonium (NH4+) in both sea fog water and rainwater were similar. These results reveal that sea fog scavenged NO3− and biogenic sulfur species more efficiently than rain. Mean dry, wet, and sea fog deposition fluxes for atmospheric total inorganic N (TIN; i.e. NH4+ + NO3−) over the subarctic western North Pacific Ocean were estimated to be 4.9 μmol m−2 d−1, 33 μmol m−2 d−1, and 7.8 μmol m−2 d−1, respectively. While NO3− was the dominant inorganic N species in dry and sea fog deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH4+. The contribution of dry, wet, and sea fog deposition to total deposition flux for TIN (46 μmol m−2 d−1) were 11%, 72%, and 17%, respectively, suggesting that ignoring sea fog deposition would lead to underestimate of the total influx of atmospheric inorganic N into the subarctic western North Pacific Ocean, especially in summer periods.

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Ecosystem model-based approach for modeling the dynamics of <sup>137</sup>Cs transfer to marine plankton populations: application to the western North Pacific Ocean after the Fukushima nuclear power plant accident

Biogeosciences ◽

10.5194/bg-13-499-2016 ◽

2016 ◽

Vol 13 (2) ◽

pp. 499-516 ◽

Cited By ~ 14

Author(s):

M. Belharet ◽

C. Estournel ◽

S. Charmasson

Keyword(s):

Power Plant ◽

Nuclear Power Plant ◽

Pacific Ocean ◽

Dose Rate ◽

North Pacific ◽

Nuclear Power ◽

Western North Pacific ◽

North Pacific Ocean ◽

Ecosystem Model ◽

Western North Pacific Ocean

Abstract. Huge amounts of radionuclides, especially 137Cs, were released into the western North Pacific Ocean after the Fukushima nuclear power plant (FNPP) accident that occurred on 11 March 2011, resulting in contamination of the marine biota. In this study we developed a radioecological model to estimate 137Cs concentrations in phytoplankton and zooplankton populations representing the lower levels of the pelagic trophic chain. We coupled this model to a lower trophic level ecosystem model and an ocean circulation model to take into account the site-specific environmental conditions in the area. The different radioecological parameters of the model were estimated by calibration, and a sensitivity analysis to parameter uncertainties was carried out, showing a high sensitivity of the model results, especially to the 137Cs concentration in seawater, to the rates of accumulation from water and to the radionuclide assimilation efficiency for zooplankton. The results of the 137Cs concentrations in planktonic populations simulated in this study were then validated through comparison with the data available in the region after the accident. The model results have shown that the maximum concentrations in plankton after the accident were about 2 to 4 orders of magnitude higher than those observed before the accident, depending on the distance from FNPP. Finally, the maximum 137Cs absorbed dose rate for phyto- and zooplankton populations was estimated to be about 5  ×  10−2 µGy h−1, and was, therefore, lower than the predicted no-effect dose rate (PNEDR) value of 10 µGy h−1 defined in the ERICA assessment approach.

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