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Temporal changes in cesium-137 (137Cs) concentrations in the surface (0–10 cm) layer of seabed sediment were quantified from continuous observation data at 71 stations within a 150-km radius of the Fukushima Daiichi Nuclear Power Plant, and the primary processes affecting temporal changes were identified. From March 2011 to the end of 2015, about 80% of the initially deposited 137Cs in the surface sediment in the coastal region (bottom depth ≤100 m) region has dissipated (radioactive decay is not included). Such a remarkable change in the 137Cs concentration was not observed in the offshore (>100 m) region. This paper focuses on the following three processes that affected the decrease in the 137Cs concentrations, and assesses their relative importance; (1) resuspension and transport of 137Cs-bound sediment, (2) desorption of 137Cs from the sediment, and (3) dilution of 137Cs by vertical mixing of sediment. Consequently, it was estimated that the first two processes together have potentially contributed to reduce the 137Cs inventory in the top 10 cm of the coastal region by at most 35%. Furthermore, by applying a pulse input sediment mixing model to the observed vertical distribution of sedimentary 137Cs, it was also estimated that more than 43% of the 137Cs in the surface sediment was transported to deeper sediment layers by vertical mixing of the sediment. This indicates that the decrease of 137Cs concentrations in coastal sediments was mainly affected by mixing of 137Cs-bound surface sediment with less contaminated sediment in the deeper layers.  相似文献   
2.
60Co were detected in common octopus specimens collected in the East China Sea in 1996-2005. The source of 60Co has remained unclear yet. Stable isotope analyses showed that there was no difference in stable Co concentrations between octopus samples with 60Co and without 60Co. This result showed that the stable Co in the digestive gland of octopus potentially did not include a trace amount of 60Co and the source of 60Co existed independently. Furthermore, investigations of octopus in other area and other species indicated that the origin of the source of 60Co occurred locally in the restricted area in the East China Sea and not in the coastal area of Japan. Concentrations of 60Co have annually decreased with shorter half-life than the physical half-life. This decrease tendency suggests that the sources of 60Co were identical and were temporary dumped into the East China Sea as a solid waste.  相似文献   
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Preface     
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4.
Hydrographic observations have revealed detailed structure of the Bottom Water in the Japan Sea. The Yamato Basin Bottom Water (YBBW) exhibits higher temperatures and lower dissolved oxygen concentrations than those found in the Japan Basin Bottom Water (JBBW). Both Bottom Waters meet around the boundary region between the Yamato and the Japan Basins, forming a clear benthic front. The structure of the benthic front suggests an estuary-like water exchange between both Basins, with the inflow from the Japan Basin passing under the outflow from the Yamato Basin. It is inferred from the property distributions that the JBBW flowing into the Yamato Basin is entrained by the cyclonic circulation in the basin, and modified to become the YBBW. Vertical diffusion and thermal balance in the YBBW are examined using a box model. The results show that the effect of geothermal heating has about 70% of the magnitude of the vertical thermal diffusion and both terms cancel the advection term of the cold JBBW from the Japan Basin. The box model also estimates the turnover time and vertical diffusivity for the YBBW as 9.1 years and 3.4 × 10−3 m2s− 1, respectively.  相似文献   
5.
Microspherules in Paleozoic-Mesozoic bedded chert, presumed to be of extraterrestrial origin and comprised of clusters of iron needles,may represent an early stage in the aggregation of the inner planets. A fraction of the constituent iron needles will be expected to be carried along with expanding gas to the periphery of the solar nebula where the outer planets and comets condensed. A substantial fraction of iron needles would escape into interstellar space and add to the population of interstellar grains. Iron needles could contribute substantially to interstellar polarization and to the infrared opacity of the interstellar medium.  相似文献   
6.
129I is one of the three major radiation risk contributors to the public as a consequence of past nuclear processing activities at Department of Energy (DOE) facilities. Elevated levels of 129I are present in the surface soils of F-Area of Savannah River Site, which used to be an isotope separation facility for the production of nuclear weapons components. The 129I in soils is thought to be bound predominantly to soil organic matter (SOM). Measurements of stable 127I and radioactive 129I in humic acids (HAs) and fulvic acids (FAs) obtained by five successive alkaline, two glycerol and one citric acid-alkaline extraction, demonstrated that these extractable humic substances (HS) together account for 54-56% and 46% of the total 127I and 129I in the soil, respectively. The remainder was likely bound to residual SOM. The iodine content (μg-I/g-C) generally decreased with each subsequent extract, while 129I/127I increased concurrently. The coincident variations in chemical compositions, aromaticity (estimated by UV spectroscopy), functional groups (e.g., aliphatic), degree of humification, relative migration in the hydrophobic interaction column, and molecular weight indicated that: (1) iodine in different HAs was bound to a small-size aromatic subunit (∼10 kDa); (2) the large-size subunit (∼90 kDa), which likely linked the small-size unit through some weak chemical forces (hydrogen bonds, hydrophobic or electrostatic interactions), determined the relative mobility of iodine bound to organic matter; (3) from the strong correlation between iodine content and aromaticity in the HAs, we suggested that iodine incorporation into the SOM via covalent aromatic C-I bond is the key mechanism controlling iodine behavior in this system. However, this relationship is not universal for all fractions of organic matter as evidenced from the different slopes of this relationship at the two sampling sites, as well as from the different relationships for HAs and FAs, respectively. These differences in iodination are due to different SOM molecular sizes, compositions, and availability of preferred iodination sites. 129I in the soil downstream from the contaminated site and near a wetland abruptly dropped below our detection limit (0.5 pCi-129I/g-soil), which suggests that the high SOM in the plume soil around the 129I-contaminated F-Area might be a natural barrier to scavenge radioiodine released from the nuclear waste repository by forming organo-iodine compounds. Soil resuspension experiments showed that mobile 129I was mostly associated with a low average molecular weight amphiphilic organic carrier (13.5-15 kDa). SOM clearly behaves as a sink for iodine at the Savannah River Site F-Area. However, this work demonstrates that a small fraction of the SOM can also behave as a source, namely that a small fraction that may be readily dispersible under some environmental conditions and presumably release iodine in the organic-colloidal form. This radioiodinated organo-colloid likely can get into the groundwater through infiltration or surface runoff where it might migrate further into the wetlands. Results from this study provide the geochemical basis for future 129I migration controls, remediation, and/or land-groundwater management strategies.  相似文献   
7.
A numerical experiment is carried out to reproduce distribution of concentration of 90Sr and 137Cs, estimate their total amount and verify their source in the Japan Sea. Model results are in good agreement with observational findings in the Japan Sea expeditions between 1997 and 2002 by the Japan Atomic Energy Agency. Vertical profiles of the concentration of 90Sr and 137Cs show exponential decreases with depth from the sea surface to the sea bottom. From the model and observational results, it is suggested that the concentration of 90Sr and 137Cs in the surface layer is approximately in the range of 1.0–1.5 Bq/m3 and 2.0–2.5 Bq/m3, respectively. On the other hand, it is found that the concentration in the intermediate and deep layer is higher than that observed in the northwestern Pacific Ocean, suggesting active winter convection in the Japan Sea. The total amount of 90Sr and 137Cs in the seawater is evaluated to be 1.34 × 1015 Bq and 2.02 × 1015 Bq, respectively, in the numerical experiment, which demonstrates an estimation by observational data obtained in the Japan Sea expeditions. The total amount of 90Sr and 137Cs changed during the second half of 20th century corresponding to deposition at the sea surface with the maximums of 4.86 × 1015 Bq for 90Sr and 7.33 × 1015 Bq for 137Cs, respectively, in the mid-1960s. The numerical experiment suggests that the main source of 90Sr and 137Cs has been global fallout, although there have been some potential sources in the Japan Sea.  相似文献   
8.
Settling particles play an important role in transporting organic carbon from the surface to the deep ocean. It is known that major components of settling particles are biogenic silicates (opal), biogenic carbonate (CaCO3), lithogenic clays and organic matter. Since each component aggregates and/or takes in organic carbon, all of these components have the ability to transport particulate organic carbon (POC) to the interior of the ocean. In this study, sediment trap experiments were carried out in four areas of the western North Pacific (including a marginal sea). Factors are proposed that correlate the composition of settling particles with POC flux. Annual mean organic carbon fluxes at 1 km depth in the western North Pacific Basin, Japan Sea, Hidaka Basin and northern Japan Trench were found to be 14.9, 18.1, 13.0 and 6.6 mg/m2/day, respectively. Organic carbon flux in the western North Pacific was greater than that in the Eastern North Pacific (7.4), the Equatorial Pacific (4.2), the Southern Ocean (5.8) and the Eastern North Atlantic (1.8). In the western North Pacific, it was calculated that 52% of POC was carried by opal particles. Opal is known to be a major component even in the Eastern North Pacific and the Southern Ocean, and the opal fluxes in these areas are similar to those in the western North Pacific. However, the organic carbon flux that was carried by opal particles (OCopalflux) in the western North Pacific was greater than that in the Eastern North Pacific and the Southern Ocean. These results indicate that the ability of opal particles to transport POC to the deep ocean in the western North Pacific is greater than that in the other areas.  相似文献   
9.
Seasonal and spatial variations of particulate organic carbon (POC) flux were observed with sediment traps at three sites in the Japan Sea (western and eastern Japan Basin and Yamato Basin). In order to investigate the transport processes of POC, radiocarbon (14C) measurements were also carried out. Annual mean POC flux at 1 km depth was 30.7 mg m−2day−1 in the western Japan Basin, 12.0 mg m−2day−1 in the eastern Japan Basin and 23.8 mg m−2day−1 in the Yamato Basin. At all stations, notably higher POC flux was observed in spring (March–May), indicating biological production and rapid sinking of POC in this season. Sinking POC in the high flux season showed modern Δ14C values (>0‰) and aged POC (Δ14C < −40‰) was observed in winter (December–January). The Δ14C values in sinking POC were negatively correlated with aluminum concentration, indicating that Δ14C is strongly related to the lateral supply of lithogenic materials. The Δ14C values also showed correlations with excess manganese (Mnxs) concentrations in sinking particles. The Δ14C-Mnxs relationship suggested that (1) the majority of the aged POC was advected by bottom currents and incorporated into sinking particles, and (2) some of the aged POC might be supplied from the sea surface at the trap site as part of terrestrial POC. From the difference in the Δ14C-Mnxs relationships between the Japan Basin and the Yamato Basin, we consider that basin-scale transport processes of POC occur in the Japan Sea.  相似文献   
10.
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