50 research outputs found
Radiocesium Contamination Histories of Japanese Flounder (Paralichthys olivaceus) After the 2011 Fukushima Nuclear Power Plant Accident
Mechanisms controlling dissolved iron distribution in the North Pacific : a model study
Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 116 (2011): G03005, doi:10.1029/2010JG001541.Mechanisms controlling the dissolved iron distribution in the North Pacific are investigated using the Biogeochemical Elemental Cycling (BEC) model with a resolution of approximately 1° in latitude and longitude and 60 vertical levels. The model is able to reproduce the general distribution of iron as revealed in available field data: surface concentrations are generally below 0.2 nM; concentrations increase with depth; and values in the lower pycnocline are especially high in the northwestern Pacific and off the coast of California. Sensitivity experiments changing scavenging regimes and external iron sources indicate that lateral transport of sedimentary iron from continental margins into the open ocean causes the high concentrations in these regions. This offshore penetration only appears under a scavenging regime where iron has a relatively long residence time at high concentrations, namely, the order of years. Sedimentary iron is intensively supplied around continental margins, resulting in locally high concentrations; the residence time with respect to scavenging determines the horizontal scale of elevated iron concentrations. Budget analysis for iron reveals the processes by which sedimentary iron is transported to the open ocean. Horizontal mixing transports sedimentary iron from the boundary into alongshore currents, which then carry high iron concentrations into the open ocean in regions where the alongshore currents separate from the coast, most prominently in the northwestern Pacific and off of California.This work was supported
by the U.S. National Science Foundation (EF‐0424599)
Improvement of 137Cs analysis in small volume seawater samples using the Ogoya underground facility
The SOLAS air-sea gas exchange experiment (SAGE) 2004
Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Deep Sea Research Part II: Topical Studies in Oceanography 58 (2011): 753-763, doi:10.1016/j.dsr2.2010.10.015.The SOLAS air-sea gas exchange experiment (SAGE) was a multiple-objective study investigating
gas-transfer processes and the influence of iron fertilisation on biologically driven gas exchange in
high-nitrate low-silicic acid low-chlorophyll (HNLSiLC) Sub-Antarctic waters characteristic of the
expansive Subpolar Zone of the southern oceans. This paper provides a general introduction and
summary of the main experimental findings. The release site was selected from a pre-voyage desktop
study of environmental parameters to be in the south-west Bounty Trough (46.5°S 172.5°E) to the
south-east of New Zealand and the experiment conducted between mid-March and mid-April 2004. In
common with other mesoscale iron addition experiments (FeAX’s), SAGE was designed as a
Lagrangian study quantifying key biological and physical drivers influencing the air-sea gas exchange
processes of CO2, DMS and other biogenic gases associated with an iron-induced phytoplankton
bloom. A dual tracer SF6/3He release enabled quantification of both the lateral evolution of a labelled
volume (patch) of ocean and the air-sea tracer exchange at the 10’s of km’s scale, in conjunction with
the iron fertilisation. Estimates from the dual-tracer experiment found a quadratic dependency of the
gas exchange coefficient on windspeed that is widely applicable and describes air-sea gas exchange in strong wind regimes. Within the patch, local and micrometeorological gas exchange process studies (100 m scale) and physical variables such as near-surface turbulence, temperature microstructure at the interface, wave properties, and wind speed were quantified to further assist the development of gas exchange models for high-wind environments.
There was a significant increase in the photosynthetic competence (Fv/Fm) of resident phytoplankton
within the first day following iron addition, but in contrast to other FeAX’s, rates of net primary
production and column-integrated chlorophyll a concentrations had only doubled relative to the
unfertilised surrounding waters by the end of the experiment. After 15 days and four iron additions
totalling 1.1 tonne Fe2+, this was a very modest response compared to the other mesoscale iron
enrichment experiments. An investigation of the factors limiting bloom development considered co-
limitation by light and other nutrients, the phytoplankton seed-stock and grazing regulation. Whilst
incident light levels and the initial Si:N ratio were the lowest recorded in all FeAX’s to date, there was
only a small seed-stock of diatoms (less than 1% of biomass) and the main response to iron addition
was by the picophytoplankton. A high rate of dilution of the fertilised patch relative to phytoplankton
growth rate, the greater than expected depth of the surface mixed layer and microzooplankton grazing
were all considered as factors that prevented significant biomass accumulation. In line with the limited
response, the enhanced biological draw-down of pCO2 was small and masked by a general increase in pCO2 due to mixing with higher pCO2 waters. The DMS precursor DMSP was kept in check through grazing activity and in contrast to most FeAX’s dissolved dimethylsulfide (DMS) concentration declined through the experiment. SAGE is an important low-end member in the range of responses to iron addition in FeAX’s. In the context of iron fertilisation as a geoengineering tool for atmospheric CO2 removal, SAGE has clearly demonstrated that a significant proportion of the low iron ocean may not produce a phytoplankton bloom in response to iron addition.SAGE was jointly funded through
the New Zealand Foundation for Research, Science and Technology (FRST) programs
(C01X0204) "Drivers and Mitigation of Global Change" and (C01X0223) "Ocean
Ecosystems: Their Contribution to NZ Marine Productivity." Funding was also provided for
specific collaborations by the US National Science Foundation from grants OCE-0326814
(Ward), OCE-0327779 (Ho), and OCE 0327188 OCE-0326814 (Minnett) and the UK Natural
Environment Research Council NER/B/S/2003/00282 (Archer). The New Zealand
International Science and Technology (ISAT) linkages fund provided additional funding
(Archer and Ziolkowski), and the many collaborator institutions also provided valuable
support
Supplementary material to "Surface pathway of radioactive plume of TEPCO Fukushima NPP1 released <sup>134</sup>Cs and <sup>137</sup>Cs"
Surface pathway of radioactive plume of TEPCO Fukushima NPP1 released <sup>134</sup>Cs and <sup>137</sup>Cs
134Cs and 137Cs were released to the North Pacific Ocean by two major likely pathways, direct discharge from the Fukushima NPP1 accident site and atmospheric deposition off Honshu Islands of Japan, east and northeast of the site. High density observations of 134Cs and 137Cs in the surface water were carried out by 17 cruises of cargo ships and several research vessel cruises from March 2011 till March 2012. The main body of radioactive surface plume of which activity exceeded 10 Bq m−3 travelled along 40° N and reached the International Date Line on March 2012, one year after the accident. A distinct feature of the radioactive plume was that it stayed confined along 40° N when the plume reached the International Date Line. A zonal speed of the radioactive plume was estimated to be about 8 cm s−1 which was consistent with zonal speeds derived by Argo floats at the region
Simulations of chlorofluorocarbons in and around the Sea of Okhotsk : Effects of tidal mixing and brine rejection on the ventilation
Ventilation of waters in and around the Sea of Okhotsk was investigated using simulations of chlorofluorocarbons (CFCs) in the northwestern North Pacific. We used an ocean general circulation model coupled with a sea ice model. The model reproduces the distributions of CFCs similar to observed values and indicates the importance of tidal mixing along the Kuril Islands and brine rejection to ventilation of waters in and around the Sea of Okhotsk. To clarify the role of each process, numerical experiments excluding one of the two processes were carried out. Results show that brine rejection transports CFCs into the intermediate layer as deep as 200-400 m along the path of dense shelf water in the western Sea of Okhotsk, but hardly to other areas and layers. On the other hand, tidal mixing transports CFCs into the intermediate and deeper layers throughout the Sea of Okhotsk. We conclude that the tidal mixing has a greater influence than brine rejection on the ventilation of layers below the winter mixed layer
