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1.
Investigations including a bathymetric survey, sonic prospecting, and vibrocoring were performed to understand the horizontal and vertical distribution of 137Cs in seabed sediments in shallow seas with depths less than 30 m near the Fukushima Daiichi Nuclear Power Plant. Especially, features of 137Cs distributions in deeper sections of the seabed sediments were studied to evaluate the vertical heterogeneity of 137Cs distribution in the seabed sediments in shallow seas. The distribution area of the seabed sediments was less than half of the investigation area, and the locations of the seabed sediments were divided into flat and terrace-like seafloors based on their topographical features. The thicknesses of the seabed sediment layers were mostly <2 m. The 137Cs inventories in the seabed sediments varied from 13 ± 1 to 3,510 ± 26 kBq m?2, and continuous distributions of 137Cs at depths greater than 81 cm were observed. The 137Cs distributions were not uniform; however, the 137Cs inventories tended to be larger near the base of the steeper ascending slopes than in the terrace-like seafloors themselves. Based on the relationship between the 137Cs inventories and mean shear stress, features of the seafloor topography were inferred to be significant control factors governing the horizontal and vertical distribution of 137Cs in the seabed sediments. Rapid changes and multiple peaks in the vertical profile of the 137Cs distributions suggest that they are related to pulse input caused by heavy-rain events. Change in the 137Cs inventories with depth in this study are larger than those reported in previous studies, indicating earlier results of 137Cs inventories per unit in seabed sediments in shallow seas, especially near the river mouth, which drains a radiologically highly-contaminated basin, were underestimated.  相似文献   

2.
In 2014 and 2015, we examined the spatial distribution of cesium-134 (half-life: 2.06 years) from the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) in marine sediments within coastal–basin areas (water depths of 40–520 m) off central Honshu Island (the main island of Japan) in the Sea of Japan. The 134Cs concentrations in both the surface sediment (0–1 cm depth) and whole-core inventory exhibited wide variations, and were highest at the site closest to the Agano River Estuary area (6.7 Bq/kg-dry and 886 Bq/m2, respectively). This indicates that 134Cs in coastal areas was delivered by riverine suspended solids (SS). Given the spatial variation in 134Cs concentrations, we believe that 134Cs partially migrated northeastward within ~50 km along Honshu Island (at water depths shallower than ~140 m), and southwestward, including the Sado Basin area. This is predominantly attributable to the transport of SS by bottom currents and unsteady downward delivery onto the steep slopes of the basin. The total amount of 134Cs in the study area in 2014 was estimated at approximately 0.6 TBq (decay-corrected to March 11, 2011, date of FDNPP accident).  相似文献   

3.
Radioactivity has been monitored in seafloor sediments off Fukushima and nearby prefectures regularly. During the initial monitoring period (May–September 2011), 137Cs concentrations in the surface sediments (0–3 cm) generally increased to 8–580 Bq/kg. Subsequently, concentrations decreased at variable rates. In the latest data, from February 2016, concentrations were still higher at 0.8–141 Bq/kg than the pre-accident level. The geometric mean concentration declined steadily from 47 Bq/kg in September 2011 to 13 Bq/kg in February 2016. The 137Cs abundance (Bq/m2) in the surface sediment at each station decreased similarly. The rate of decrease of surface abundance varied spatially by almost one order of magnitude, ranging from 1.1 × 10?4 to 1.7 × 10?3/day, equivalent to halving times of 16–1.1 years, respectively. The rate of decrease was related to the median sediment grain size at each station. In addition, bottom-water dynamics, through the redistribution of bottom sediments, may have caused spatial variability in the rate of decrease, whereas vertical profiles of 137Cs concentrations in the sediment suggest that vertical migration of 137Cs was not a major mechanism reducing the surface 137Cs concentration. From September 2011 to February 2016, the overall halving time of 137Cs in the surface sediment in the monitoring area, excluding the area inside a 30-km radius from the Fukushima Dai-ichi Nuclear Power Plant, was 2.3 years. Thus, 76% of the originally deposited 137Cs (46 × 1012 Bq) in the surface sediment was transported out of the area during that period.  相似文献   

4.
The Fukushima nuclear accident in 2011 released large amounts of radionuclides, including ~(137)Cs, into the Pacific Ocean. A quasi-global ocean radioactive transport model with horizontal grid spacing of 0.5°×0.5° and 21 vertical layers was thereafter established to study the long-term transport of the Fukushima-derived ~(137)Cs in the ocean.The simulation shows that the plume of ~(137)Cs would be rapidly transported eastward alongside the Kuroshio Current and its extensions. Contaminated waters with concentrations lower than 2 Bq/m3 would reach the west coast of North America 4 or 5 years after the accident. The ~(137)Cs tends to be carried, despite its very low concentration, into the Indian and South Pacific Oceans by 2016 via various branches of ocean currents.Meanwhile, the ~(137)Cs concentrations in the western part of the North Pacific Ocean decrease rapidly with time. Up to now the highly contaminated waters have remained in the upper 400 m, showing no evidence of significant penetration to deeper layers.  相似文献   

5.
The concentrations of90Sr and137Cs, derived from the radioactive fallout, in the surface layers of the adjacent seas of Japan and the North Pacific were determined radiochemically during 1969 to 1973. The90Sr and137Cs concentrations in sea water decreased markedly with increase of the depth and below the depth of 1,000 m, the concentrations were approximately uniform. The distribution of90Sr in the surface water of the North Pacific in spring of 1970 was approximately uniform, except two regions; rather large low-concentration region between 160°E and 170°W and relatively higher contamination area around 32°N and 146°W.  相似文献   

6.
-The applicability of the doubie-layer model for 210Pb chronology in coastal marine environments was discussed,which is successfully used in the study of mixing rates and sedimentation rates in Meizhou Bay. Differences among sedimentation rates deduced from 210Pb, 210Po, and 137Cs were compared. Mixing rates in the sediment surface layer were determined by means of excess 234Th.  相似文献   

7.
Salt marsh sediment volume decreases from organic decomposition, compaction of solids, and de-watering, and each of these processes may change with age. Variability in the vertical accretion rate within the upper 2 m was determined by assembling results from concurrent application of the 137Cs and 210Pb dating techniques used to estimate sediment age since 1963/1964, and 0 to ca 100+ years before present (yBP), respectively. The relationship between 210Pb and the 137Cs dated accretion rates (Sed210 and Sed137, respectively) was linear for 45 salt marsh and mangrove environments. Sed210 averaged 75% of Sed137 suggesting that vertical accretion over the last 100+ years is driven by soil organic matter accumulation, as shown for the pre 137Cs dated horizon. The ratio of Sed210/Sed137 declines with increasing mineral content. A linear multiple regression equation that includes bulk density and Sed137 to predict Sed210 described 97% of the variance in Sed210. Sediments from Connecticut, Delaware and Louisiana coastal environments dated with 14C indicate a relatively constant sediment accretion rate of 0.13 cm year−1 for 1000–7000 yBP, which occurs within 2 m of today's marsh surface and equals modern sea level rise rates. Soil subsidence is not shown to be distinctly different in these vastly different coastal settings. The major reason why the Sed137 measurements indicate higher accretion rates than do the Sed210 measurements is because the former apply to younger sediments where the effects of root growth and decomposition are greater than in the latter. The most intense rates of change in soil volume in organic-rich salt marshes sediments is, therefore, neither in deep or old sediments (>4 m; >1000 years), but within the first several hundreds of years after accumulation. The average changes in organic and inorganic constituents downcore are nearly equal for 58 dated sediment cores from the northern Gulf of Mexico. These parallel changes downcore are best described as resulting from compaction, rather than from organic matter decomposition. Thus most of the volumetric changes in these salt marsh sediments occurs in the upper 2 m, and declines quickly with depth. Extrapolation forwards or backwards, using results from the 210Pb and the 137Cs dating technique appear to be warranted for the types of samples from the environments described here.  相似文献   

8.
We used more than 25,000 nutrient samples to elucidate for the first time basin-scale distributions and seasonal changes of surface ammonium (NH4 +) and nitrite (NO2 ?) concentrations in the Pacific Ocean. The highest NH4 +, NO2 ?, and nitrate (NO3 ?) concentrations were observed north of 40°N, in the coastal upwelling region off the coast of Mexico, and in the Tasman Sea. NH4 + concentrations were elevated during May–October in the western subarctic North Pacific, May–December in the eastern subarctic North Pacific, and June–September in the subtropical South Pacific. NO2 ? concentrations were highest in winter in both hemispheres. The seasonal cycle of NH4 + was synchronous with NO2 ?, NO3 ?, and satellite chlorophyll a concentrations in the western subtropical South Pacific, whereas it was synchronous with chlorophyll-a but out of phase with NO2 ? and NO3 ? in the subarctic regions.  相似文献   

9.
Historical sediment nutrient concentrations and heavy metal distributions were studied in four estuaries in the Gulf of Finland, Baltic Sea to examine the response of these estuaries to temporal changes in human activities. Cores were collected using a 1-m Mackereth corer and dated using 210Pb and 137Cs. The cores were analyzed for total carbon (TC), total nitrogen (TN), total phosphorus (TP), organic phosphorus (OP), inorganic phosphorus (IP), biogenic silica (BSi), loss-on-ignition (LOI), Cu, Zn, Al, Fe, Mn, K, Ca, Mg and Na. Principal component analysis (PCA) was used to summarize the trends in the chemical variables and to compare the trends at the different sites. Applying the 1986 137Cs date as a reference point, 210Pb chronologies were constructed for the sites using either the CRS model or a composite model (using both CIC and CRS). Significant increases were observed in sedimentation rates, TP and TN concentrations in all of the cores. Copper showed clear increases from 1850 towards present at all sites. Furthermore, redundancy analysis (RDA) was used to correlate environmental variables (catchment land use, catchment size, estuary surface area, depth and lake percentage) to sediment geochemistry. Based on redundancy analysis (RDA), the percentage of agriculture in the catchment was the most important factor affecting the sediment accumulation rate. Urban land-use types and industry correlate well with sediment Cu and Ca concentrations. Forest areas were related to high sediment BSi concentrations. Catchment land use was the most significant factor affecting sediment geochemical composition and sediment accumulation rates in these coastal embayments. Our results demonstrate that the coastal estuaries of the Gulf of Finland respond to the increased nutrient loading with the increased sedimentation and nutrient accumulation rates.  相似文献   

10.
Analysis of 210Pb, 226Ra, 137Cs and 134Cs in short sediment cores provide first estimates of deposition rates in some Clyde sea lochs. The radio-caesium nuclides originate mainly in the liquid effluent released at distance from the Clyde by the Windscale nuclear fuel reprocessing plant and their concentrations in Clyde sediments provide information on (a) enrichment factors onto particulate matter, (b) surficial mixing coefficients and (c) sedimentation rates. A radiocaesium residence time in coastal waters of ca. 103 years reflects the importance of scavenging by the high nearshore particulate flux. 210Pb levels in sediments are controlled, in the unsupported fraction, by a major input sorbed on catchment particulates and, in the supported component, by 226Ra activities occasionally perturbed by unusually high surface values probably of planktonic origin. In one loch, detectable levels of 134Cs and 60Co are attributed to their discharge by nuclear submarines.  相似文献   

11.
Radionuclide measurements have been conducted on sediment cores collected in 1992 in the south-eastern region of the Barents Sea, known as the Pechora Sea. Cesium-137 and 239,24OPu activities in surface sediments are generally less than 30 Bq/kg, with the highest levels being measured in sediments off the southwestern coastline of the island of Novaya Zemlya. High correlations between both 137Cs and 239,24OPu and the concentration of fine (< 63 μm) particles in surface sediments indicate that much of the variance in radionuclide concentrations throughout the Pechora Sea can be explained by particle size fractionation. However, elevated activities of 137Cs (138 Bq/kg), 60Co (92 Bq/kg), 241Am (433 Bq/kg), and especially 239,24OPu (8.47 × 103 Bq/kg) were measured in one surface sediment sample from the fjord of Chernaya Bay on the southern coast of Novaya Zemlya. The source of radioactive contamination is two underwater nuclear tests conducted in Chernaya Bay in 1955 and 1957.The 238Pu/239,240Vu activity ratio of 0.0245 in Chernaya Bay is equivalent to values measured in global fallout. The 240Pu/239Pu atom ratio (0.0304), measured by mass spectrometry, is much lower than values (0.18) typical of global fallout, but is consistent with ratios measured for fallout from the early (1951–1955) series of weapons tests at the Nevada Test Site. The timing of the Chernaya Bay source term, estimated from the 241Am/241Pu ratio, is consistent with the timing of the 1955 and 1957 underwater nuclear tests. Relatively low initial yields of 241Pu (241Pu/239Pu atom RATIO = 0.00 123) in these tests have resulted in relatively low 241Am/239,240Pu activity ratios (0.05) in recent sediments in Chernaya Bay.Radionuclide tracer profiles in cores from the Pechora Sea can be simulated using a two-layer biodiffusion model with rapid, near-homogeneous mixing in the surface mixed layer and reduced mixing in the deep layer. Lead-210 profiles are consistent with a wide range of sedimentation and mixing rates in the deep sediment layer. However, the 137Cs and 239,240Pu results further constrain the model parameters and indicate that the downward transport of radionuclides in the sediments is governed primarily by sediment mixing, with sediment burial playing a secondary role.  相似文献   

12.
《Marine Geology》2005,216(4):249-263
Bottom sediments collected in the Northwest (NW) Pacific Ocean in 1997 were analysed for 90Sr, 137Cs, 239,240Pu and 241Am contents to determine their distribution patterns, inventories and sources. Enhanced inventories of 239,240Pu and 241Am were observed in the latitudinal belts of 10–20°N and 30–40°N, which correspond to major areas of local (tropospheric) and global (stratospheric) fallout (with a contribution from local fallout), respectively. The sediment inventory of 239,240Pu near the Bikini Atoll exceeded its overlying water inventory, however, in the mid-latitudes, more than 70% of 239,240Pu still remains in the water column. 241Am inventories in sediments exceeded that of the water column for the entire NW Pacific Ocean. Higher 137Cs and 90Sr sediment inventories in the latitudinal belt of 30–40°N are due to global fallout, and they account for about 10% and less than 5% of the water column inventories, respectively. The observed activity ratios of 137Cs/90Sr, 238Pu/239,240Pu and 241Am/239,240Pu in sediment were at some stations higher than the global fallout ratios due to contributions from local fallout and due to specific processes in the water column. Two end-member mixing model based on the 240Pu/239Pu atom ratios observed in global and local fallout yielded ∼60% contribution of the local fallout in the bottom sediments near the Bikini Atoll. The upward decrease in the 240Pu/239Pu atom ratios in the sediment column indicates a decrease in the contribution of local fallout to the Pu inventory with time. 241Am and 241Pu dating of sediment layers was utilized to explain a hiatus in sediment accumulation in the deep seafloor.  相似文献   

13.
Contents of90Sr,137Cs and60Co in surface sediments were investigated in and around Urazoko Bay, Fukui Prefecture, where a nuclear power plant has been operating since 1969 and the waste effluent has been released into the sea. The main source of90Sr and137Cs was recognized to be radioactive fallout, whereas60Co was considered to originate from the nuclear power plant. Using the137Cs concentration as an indicator of sorption capacity of the sediment, the behaviour of60Co was investigated. No seasonal variation was observed in the distribution pattern of60Co/137Cs ratio and the retention of the heavy initial discharge in 1969 was considered to dominate the radionuclide level in the sediment. Correlation of60Co/137Cs ratio in the sediment and the distance from the discharge outlet was expressed by a simple exponential function of the distance. It was suggested that the contamination is spreading out gradually to the outer region of Urazoko Bay.  相似文献   

14.
The activity concentrations of dissolved137Cs have been determined in the water column and137Cs and134Cs in the sediments and the sediment porewaters of the southern Baltic Sea. The mean activity concentration of dissolved137Cs in the Gdansk Deep declined from 109 Bq m−3in June 1986 to 61 Bq m−3in 1999. In sediments, the activity concentrations of137Cs (33-231 Bq kg−1) were highest in muds and the activity concentrations of134Cs were about 6% of the total Cs activity. The Chernobyl contribution to137Cs activity was between 43% and 77%. The porewater activity concentrations of137Cs in muddy sediments were in the range 71 to 3900 Bq m−3and were higher than those in the overlying seawater. The diffusive flux of dissolved137Cs from the muddy sediments was estimated in the range 5 to 480 Bq m−2year−1. The flux of137Cs from sediment porewaters of the southern Baltic Sea was about 45% of the total, including fluxes of137Cs from wet and dry atmospheric deposition and the fluvial inputs. The results were used to elucidate the rate of recovery of the sediments and the waters of the southern Baltic from Chernobyl-derived137Cs.  相似文献   

15.
In the Russian sector of the Gdansk Basin (Baltic Sea), high organic matter influx fuels microbial processes resulting in the formation of reduced sediments with elevated methane concentrations. Investigated areas of geoacoustic anomalies (～245 km2) were found to contain three distinct geomorphologic structures (pockmarks), with a total area of ～1 km2. Methane anomalies recorded in the water above one of these pockmarks were traced as high as 10 m above the bottom. In pockmark sediments, sulfate reduction and anaerobic oxidation of methane (AOM) occurred at high rates of 33 and 50 µmol dm?3 day?1, respectively. Integrated over 0–180 cm sediment depths, AOM exceeded methanogenesis almost tenfold. High AOM rates resulted from methane influx from deeper sediment layers. The δ13C signature of methane carbon (?78.1 to ?71.1‰) indicates the biogenic origin of pockmark methane. In pockmark sediments, up to 70% of reduced sulfur compounds was possibly produced via AOM.  相似文献   

16.
Abstract. Two sediment cores were collected in the southern Baltic Sea and sliced into 1.0cm-thick layers. Sediments of each layer were analysed for activities of 210Pb, 137Cs, 134Cs and for the density of meiobenthic organisms (meiofauna). Zones with the rapid mixing occur in the uppermost layers (0–3 cm) of the cores based on I34Cs profiles. The extent and density of meiofauna confirmed the rapid mixing and revealed layers with slow mixing (4–8 cm). Sedimentation rates were derived from 210Pb profiles below the mixing zones (1.21 and 1.72 mm a-I) and were confumed by 137Cs distribution. Of twenty-one major meiofauna taxa commonly found in the Baltic sediments, three were present in the cores.  相似文献   

17.
The distribution and inventory of artificial radionuclides,239,240Pu and137Cs were determined in the East China and the Yellow Seas in 1987. Almost all of239,240Pu and 50 to 80% of137Cs in the continental shelf area are retained in the sediment column.239,240Pu sediment inventory in the sea area is larger than the fallout input and tends to increase southwardly. This excess239,240Pu and the lateral distribution are attributable to the supply of239,240Pu by the Yangtze River discharge. On the contrary,137Cs sediment inventory shows a decrease to the south, and the fact can be accounted for by the southward dispersion of fine silt particles discharged from the Yellow River. Total137Cs inventory is smaller than the estimated fallout input, and the fact seems to indicate dispersion of137Cs out of the shelf region. Vertical profiles of239,240Pu and137Cs contents in sediments differ from that of natural210Pb, implying the effect of varied accumulation rates of the artificial radionuclides over the sediment particle mixing by benthic organisms. Apparent maximum sediment particle mixing coefficient (D B ) calculated from the excess210Pb profiles in stations located between the inner and outer shelves ranged from 1.4 to 8.3 cm2y–1. ThisD B value is higher than that in the Okinawa Trough (1.0 cm2y–1), but lower than previously estimatedD B value (26 cm2y–1) in the outer shelf mud.  相似文献   

18.
Sediments in the Hudson Estuary contain zinc, copper and lead from metal pollutants discharged to the harbor in the New York City area, from dispersed sources of contamination introduced upstream, and from natural weathering processes. The magnitude of the contribution from each of these three sources to particular sites can be estimated on the basis of total metal abundances, relative proportions of several metals, and other sediment properties. The pattern of recent heavy-metal contamination in Hudson sediments closely follows the distribution in sediments of 137Cs which was derived over the past two decades from global fallout and local releases from a commercial nuclear reactor. Several simple empirical corrections related to grain size and mineralogy variations are suggested for comparing heavy-metal contamination levels of sandy continental shelf sediments with fine-grained estuarine and coastal sediments. Iron has little variation in Hudson sediments while manganese is greater in surface sediment of some low-salinity and fresh-water areas than deeper in the sediments, and generally less in the high-salinity area of rapid sediment deposition in New York harbor. Much of the pollutant Cu added to the harbor appears to be rapidly deposited in the sediments.  相似文献   

19.
Large areas of the bottom sediments of the Baltic Sea are temporarily or permanently anoxic. These sediments are also an important sink for a variety of contaminants. Reoxygenation of bottom waters allows recolonisation by benthic infauna, which may have important implications for the fate of buried contaminants. This study used tracers to experimentally examine the role of bioturbation by benthic infauna in transporting sediment-associated contaminants in the Baltic Sea. Three different tracer methods were used in two experiments, using three key Baltic macrofaunal species: the amphipod crustacean Monoporeia affinis; the Baltic clam Macoma baltica; and the priapulid worm Halicryptus spinulosus. In the first experiment, a reoxygenation–recolonisation scenario was recreated in the laboratory, using hypoxic sediment cores collected in the field, to determine if there was remobilisation of buried 137Cs from the Chernobyl nuclear accident in 1986. The potential for the infauna to bury newly settled surface contamination was also investigated, using a fluorescent particle tracer. In the second experiment, artificially-created radiolabelled tracer layers (14C and 51Cr) were used to quantify both upward and downward movements of organic matter and sediment-associated contaminants by bioturbation.In both experiments there were clear visual differences between the sediment effects of the three species. Halicryptus spinulosus buried deepest into the sediment, creating a network of burrows, Monoporeia affinis burrowed actively in the upper few centimeters of the sediment, and Macoma baltica was quite stationary, but appeared to filter- and deposit feed at the sediment surface. Mixing depths in the hypoxic sediment varied from 4.0 ± 3.5 cm for M. baltica to 7.8 ± 2.1 cm for H. spinulosus. Biodiffusion rates (Db) were similar for all treatments but biotransport rates (r) were significantly different between treatments, mainly due to a high r value for H. spinulosus. In the experiment with radiolabelled tracer layers, 51Cr was transported more than 14C, and tracer originally at the surface transported more than tracer buried 4 cm below the surface. There was also transport of all tracers in treatments without added macrofauna. The most likely explanation is bioturbation by the meiofauna that were undoubtedly present in both experiments.Bioturbation by macrofauna both buries surface contaminants and remobilises those that are buried, but the effects are small and on a similar scale to transport caused by meiofauna. In addition, 137Cs profiles at the hypoxic site indicated that resuspension and redeposition of sediment by physical processes had occurred, and also showed that contaminants from the last 40 years were still present in the top 5–10 cm of the sediment, well within active mixing depths. At this site, as at many others in the Baltic, physical processes are likely to be far more important than biological processes in the redistribution of contaminants on a decadal timescale.  相似文献   

20.
Geochemical tracers, including Ba, Co, Th, 7Be, 137Cs and 210Pb, and magnetic properties were used to characterize terrestrial runoff collected in nearshore time-series sediment traps in Hanalei Bay, Kauai, during flood and dry conditions in summer 2006, and to fingerprint possible runoff sources in the lower watershed. In combination, the tracers indicate that runoff during a flood in August could have come from cultivated taro fields bordering the lower reach of the river. Land-based runoff associated with summer floods may have a greater impact on coral reef communities in Hanalei Bay than in winter because sediment persists for several months. During dry periods, sediment carried by the Hanalei River appears to have been mobilized primarily by undercutting of low 7Be, low 137Cs riverbanks composed of soil weathered from tholeiitic basalt with low Ba and Co concentrations. Following a moderate rainfall event in September, high 7Be sediment carried by the Hanalei River was probably mobilized by overland flow in the upper watershed. Ba-desorption in low-salinity coastal water limited its use to a qualitative runoff tracer in nearshore sediment. 210Pb had limited usefulness as a terrestrial tracer in the nearshore due to a large dissolved oceanic source and scavenging onto resuspended bottom sediment. 210Pb-scavenging does, however, illustrate the role resuspension could play in the accumulation of particle-reactive contaminants in nearshore sediment. Co and 137Cs were not affected by desorption or geochemical scavenging and showed the greatest potential as quantitative sediment provenance indicators in material collected in nearshore sediment traps.  相似文献   

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