首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 140 毫秒
1.
The concentrations of137Cs and134Cs were measured using the sorption method in the waters of the Black Sea during 1986–1987. An inhomogeneous character of the contamination of the surface waters in the Black Sea due to the Chernobyl disaster is shown. The subsequent migration and redistribution of caesium radionuclides in the various seasons of the year were studied. The amount of137Cs and134Cs in the upper 50 m layer was estimated. The results of measuring the concentration of caesium radionuclides in the near-water atmospheric layer over the Black Sea and Mediterranean Sea in 1986–1987 are also reported.Translated by Mikhail M. Trufanov.  相似文献   

2.
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   

3.
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   

4.
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   

5.
Concentrations and inventories of137Cs and239,240Pu were determined in sea waters and sediments columns from the western North Pacific from 1980 to 1986.The239,240Pu/137Cs activity ratio in the water column shows a tendency to increase from the surface (10–3) to bottom waters (10–1), but the ratio in sediment is within a rather narrow range (10–2 to 10–1), indicating more effective removal of plutonium from the water column than137Cs. In regions south of 40N, the radionuclide inventories in the water column significantly exceed the estimated global fallout (stratospheric fallout due to the atmospheric nuclear explosion), especially in the case of239,240Pu. These excess inventories imply that local or close-in fallout derived from nuclear explosions in the equatorial North Pacific are well-preserved and retained in the regions, despite about 20 years since the atmospheric nuclear explosion moratorium. Data suggesting lateral transport of137Cs in surface water from north of 40N to southern regions is shown. Some data on90Sr contents are also shown.  相似文献   

6.
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   

7.
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   

8.
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   

9.
The Atacama trench, the deepest ecosystem of the southern Pacific Ocean (ca. 8000 m depth) was investigated during the Atacama Trench International Expedition. Sediments, collected at three bathyal stations (1040–1355 m depth) and at a hadal site (7800 m) were analyzed for organic matter quantity and biochemical composition (in terms of phytopigments, proteins, carbohydrates and lipids), bacterial abundance, biomass and carbon production and extracellular enzymatic activities. Functional chlorophyll-a (18.0±0.10 mg m−2), phytodetritus (322.2 mg m−2) and labile organic carbon (16.9±4.3 g C m−2) deposited on surface sediments at hadal depth (7800 m) reached concentrations similar to those encountered in highly productive shallow coastal areas. High values of bacterial C production and aminopeptidase activity were also measured (at in situ temperature and 1 atm). The chemical analyses of the Atacama hadal sediments indicate that this trench behaves as a deep oceanic trap for organic material. We hypothesize that, despite the extreme physical conditions, benthic microbial processes might be accelerated as a result of the organic enrichment.  相似文献   

10.
A budget model covering the Baltic Sea was developed for the time period 1980–2000 to estimate water and dissolved silica (DSi) fluxes as well as internal DSi sinks/sources. The Baltic Sea was resolved by eight basins, where the largest basin — the Baltic Proper — was divided laterally into north/west and southern/east parts as well as vertically to take into account the existence of the permanent halocline. The basins demonstrated rather different patterns with regard to silica cycling. The Gulfs of Finland and Riga together with the northernmost basins, Bothnian Bay and Bothnian Sea, are distinguished by substantial specific rates of silica removal accounting for 1.6–4.9 g Si m− 2 yr− 1. Bearing in mind the large total primary production, the basins comprising the Baltic Proper with the specific removal rates 0.2 and 1.2 g Si m− 2 yr− 1, do not appear as regions with a high silica accumulation. The Arkona and the Kattegat mainly behave as regions of rapid through-flows. These results point out the northernmost Gulf of Bothnia, the Gulfs of Riga and Finland as areas with a larger share of biogenic silica accumulation than in the Baltic Proper. It is attributed to hydrographic and hydrochemical features. An estimate of diatom export production was made for the Baltic Proper showing that the diatom contribution accounts for 19–44% of the net export production.  相似文献   

11.
Particulate organic carbon (POC) in surface sediments of the Baltic Sea   总被引：2，自引：2，他引：0  
In this study, particulate organic carbon (POC) contents and their distribution pattern in surficial sediments of the Baltic Sea are presented for 1,471 sampling stations. POC contents range from approx. 0.1% in shallow sandy areas up to 16% in deep muddy basins (e.g. Gotland Basin). Some novel relationships were identified between sediment mass physical properties (dry bulk density (DBD), grain size) and POC levels. Notably, the highest POC concentrations (about 10–17 mg cm–3) occur in sandy mud to mud (60–100% mud content) with intermediate POC contents of about 3–7% and DBDs of 0.1–0.4 g cm–3. Areas with this range in values seem to represent the optimum conditions for POC accumulation in the Baltic Sea. The maximum POC contents (8–16%) are found in fluid mud of the central Baltic Sea characterized by extremely low DBDs (<0.1 g cm–3) and moderate POC concentrations (4–7 mg cm–3). Furthermore, sediment mass accumulation rates (MAR), based on 210Pb and 137Cs measurements and available for 303 sites of the Baltic Sea, were used for assessing the spatial distribution of POC burial rates. Overall, these vary between 14 and 35 g m–2 year–1 in the mud depositional areas and, in total, at least 3.5 (±2.9) Mt POC are buried annually. Distribution patterns of POC contents and burial rates are not identical for the central Baltic Sea because of the low MAR in this area. The presented data characterize Baltic Sea sediments as an important sink for organic carbon. Regional differences in organic carbon deposition can be explained by the origin and transport pathways of POC, as well as the environmental conditions prevailing at the seafloor (morphology, currents, redox conditions). These findings can serve to improve budget calculations and modelling of the carbon cycle in this large brackish-water marginal sea.  相似文献   

12.
The concentrations of man made radionuclides in surface seawater since early ′60s are here reported as measured in Italy and Japan. Most of the data refers to90Sr and137Cs, but occasionally the concentrations of89Sr and134Cs in some Italian samples are also given. The main sources of man made radionuclides were the global fallout produced by the nuclear weapon tests and the Chernobyl accident. The respective contributions to the contamination of surface seawater around both countries are discussed.  相似文献   

13.
An analysis of the variations in the concentrations of 137Cs and 90Sr radionuclides in the Baltic Sea surface waters after the accident at the Chernobyl nuclear power plant was performed. An instability of the 137Cs concentration values during the short-term observations was found, when these values were differed 2-to 3-fold. The concentrations of 90Sr appeared to be more stable; meanwhile, their deviations sometimes exceeded the ranges of the experimental errors. By the variations in the monthly average values of the radionuclide concentrations in the surface waters of the Baltic Sea in 1989–1995, no trend of the water self-purification was observed. The theoretical results obtained confirmed the potential of the formation and propagation of patches with increased concentrations of 137Cs in the southeastern part of the Baltic Sea. The most reliable factor that controlled the process of self-purification of the Baltic Sea water appeared to be the mean annual value of the concentration of radionuclides. Pronounced divergences were obtained between the measured and calculated mean annual concentrations of 137Cs and 90Sr radionuclides in the surface waters of the Baltic Sea in 1989–2001. These divergences are explained by the potential influence of the waters from the Gulf of Bothnia and by other additional supplies of radionuclides to the marine environment, which were not included into the mathematical models.  相似文献   

14.
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   

15.
The migratory response of intertidal microphytobenthos to changes in irradiance was studied on undisturbed estuarine sediments. Two non-destructive optical techniques were used to trace variations in vivo of surface biomass: PAM fluorometry, for measuring the minimum fluorescence level (Fo); and spectral reflectance analysis, for quantifying the normalized difference vegetation index (NDVI). Following the formation of a dense biofilm at the surface, replicated sediment samples were simultaneously exposed to six different irradiance levels, ranging from 50 to 1500 μmol m−2 s−1, during a period of 120 min. The migratory photoresponse of the biofilms was characterised by constructing biomass vs. light curves (BLC), relating the accumulation of microalgal biomass after that period (estimated by Fo or NDVI) to the irradiance level incident on the surface. BLCs allow characterising the main features of the migratory photoresponse of intact biofilms. Typical BLC showed a clear biphasic pattern, with an increase in microalgal accumulation under irradiances below 100 μmol m−2 s−1, maximum values under 100–250 μmol m−2 s−1, and a gradual decrease of surface biomass under higher irradiances, indicating a strong photophobic downward migratory response. Similar BLC patterns were obtained when measuring Fo or NDVI. The construction of BLCs for biofilms from intertidal sites with distinctive sediment characteristics and diatom taxonomic composition allowed to detected significant differences in the migratory photoresponse. Biofilms from a muddy sediment exhibited considerably larger amplitude in the migratory photoresponse than the biofilms from a sandy mud site, especially under high irradiances. The photophobic migratory response to high light was found to vary among diatom species, particularly in the case of the biofilms from the muddy sediments.  相似文献   

16.
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   

17.
Marked fluctuation of concentrations of90Sr and137Cs was observed in the bottom waters at the entrance of Wakasa Bay during 1987–1992, and the cause was investigated. The concentrations of90Sr and137Cs in the bottom waters were significantly low when the upper level of the Japan Sea Proper Water (JSPW) was high and covered the sampling depth, but high when the upper level of the JSPW was low. The cause of the fluctuation observed in the bottom waters is, therefore, suggested to be the vertical fluctuation of the upper level of the JSPW on the shelf slope, which has been little described before.  相似文献   

18.
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   

19.
The whole core squeezing method was used to simultaneously obtain profiles of nitrous oxide (N2O), nitrogenous nutrients, and dissolved oxygen in sediments of Koaziro Bay, Japan (coastal water), the East China Sea (marginal sea), and the central Pacific Ocean (open ocean). In the spring of Koaziro Bay, subsurface peaks of interstitial N2O (0.5–3.5 cm depth) were observed, at which concentrations were higher than in the overlying water. This was also true for nitrate (NO3−) and nitrite (NO2−) profiles, suggesting that the transport of oxic overlying water to the depth through faunal burrows induced in situ N2O production depending on nitrification. In the summer of Koaziro Bay, sediment concentrations of N2O, NO3− and NO2− were lower than in the overlying water. In most East China Sea sediments, both N2O and NO3− decreased sharply in the top 0.5–2 cm oxic layer (oxygen: 15–130 μM), which may have indicated N2O and NO3− consumption by denitrification at anoxic microsites. N2O peaks at subsurface depth (0.5–6.5 cm) implied in situ production of N2O and/or its supply from the overlying water through faunal burrows. However, the occurrence of the latter process was not confirmed by the profiles of other constituents. In the central Pacific Ocean, the accumulation of N2O and NO3− in the sediments likely resulted from nitrification. Nitrous oxide fluxes from the sediments, calculated using its gradient at the sediment–water interface and the molecular diffusion coefficient, were −45 to 6.9 nmolN m−2 h−1 in Koaziro Bay in the spring, −29 to −21 nmolN m−2 h−1 in the summer, −46 to 37 nmolN m−2 h−1 in the East China Sea, 0.17 to 0.23 nmolN m−2 h−1 in the equatorial Pacific, and <±0.2 nmolN m−2 h−1 in the subtropical North Pacific, respectively.  相似文献   

20.
In situ measurements of ammonium and carbon dioxide fluxes were performed using benthic chambers at the end of spring and the end of summer in two soft-bottom Abra alba communities of the western English Channel (North Brittany): the muddy sand community (5 m, about 10% of surface irradiance) and the fine-sand community (19 m, about 1% of surface irradiance). High rates of ammonium regeneration were measured in the two communities at the end of summer (296.03±40.07 and 201.7±62.74 μmolN m−2 h−1, respectively) as well as high respiration rates (2.60±0.94 and 2.23±0.59 mmolC m−2 h−1, respectively). Significant benthic gross primary production (up to 6.11 mmolC m−2 h−1) was measured in the muddy sand community but no benthic primary production was measured in the fine-sand community. It suggests that microphytobenthic production values used in simulations previously published for these two communities were overestimated while values of community respiration were underestimated. The study confirms that this benthic system is heterotrophic and strengthens the idea that an important pelagic-benthic coupling is required for the functioning in such coastal ecosystems.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号