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1.
The physico-chemical states of artificial radionuclides,90Sr,137Cs and144Ce in seawater were investigated by radiochemical analysis of filtered and unfiltered seawater. The difference of radionuclide concentrations between unfiltered and filtered seawaters was defined as the particulate form radioisotope and its particle ratio was discussed.Practically no particulate90Sr, greater than 0.22 in size, was observed in both coastal and open seawaters, but some of137Cs seemed to be insoluble in some circumstances, especially in coastal waters. A considerable amount of144Ce was found to be particulate.An estimation of the radionuclides in particulate form was made for Kashima-nada seawaters collected in 1970 to 1972, and it was shown that the possible occurrence of particulate radionuclides, greater than 0.22 in size, were 1% or less for90Sr and 6% for137Cs. In the coastal water, 80 % of144Ce were seemed to be in particulate form, but in the open seawater only a few%. The influences of suspended materials to137Cs and144Ce concentration levels in seawater were not negligible and further investigations are desirable. 相似文献
2.
90Sr and137Cs concentrations and their vertical distributions were determined in deep waters in the western Northwest Pacific, including the adjacent seas of Japan, from 1976 to 1979.The profiles of the radionuclides show distribution patterns with two parts with an exponential variation of radioisotope content with depth in both parts.Generally speaking, the inventories of90Sr and137Cs in the open waters of the northwestern Pacific correspond fairly well to the fallout inputs, but in some circumstances there seems to be considerable removal of radionuclides from the water column or they are diluted with water of lower radioactivity from other regions.The possibility of radioisotope remobilization from the bottom sediment or particulate matter is also discussed. 相似文献
3.
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
4.
V. N. Eremeev T. V. Chudinovskikh G. F. Batrakov T. M. Ivanova 《Physical Oceanography》1991,2(1):57-64
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
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.
239, 240Pu,137Cs and90Sr concentrations were determined in sea waters from the central and western North Pacific in 1980 and 1982. The results are
consistent with those reported earlier for North Pacific waters. The profiles of90Sr and137Cs show a monotonic decrease with depth, whilst239, 240Pu shows a distinct subsurface maximum at a depth between 400 and 1,000 m.
The calculated inventories of these nuclides significantly exceed the global mean fallout inputs for these latitudes. This
may be due to local fallout input to the ocean at times of large-scale nuclear weapon tests in the equatorial North Pacific.
The existence of measurable amounts of137Cs and239, 240Pu in deep waters suggests that these nuclides are transported by sinking particulate matter from the surface to the deep
ocean. 相似文献
7.
A novel approach to in situ extraction of Cs radionuclides from seawater is described which offers many advantages over previous methods. Cesium (stable and radioactive) is partially stripped from seawater as it passes in series through a tandem cartridge consisting of twin beds of ion exchange resin impregnated with cupric ferrocyanide. It is demonstrated that, when seawater passes through this cartridge at a constant flow-rate, collection efficiencies of each bed are the same, allowing the calculation of the seawater Cs nuclide concentration. The cartridge is made of inexpensive, readily available, PVC pipe fittings and is easily deployed under various field conditions. Procedures are described for resin preparation and desorption and radiochemical purification of the collected Cs. Thousands of liters of seawater can be stripped of Cs in this way, permitting substantial improvement in the sensitivity of measurement of 134Cs and 137Cs. 相似文献
8.
The discharge of radioactive waste, from nuclear fuel reprocessing facilities, into the coastal waters of north-west Europe has resulted in a significant increase in the inventories of a number of artificial radionuclides in the North Atlantic. Radiocaesium, 90Sr and 99Tc, which behave conservatively in seawater, have been used widely as tracers of water movement through the North Sea, Norwegian Coastal Current, Barents Sea, Greenland Sea, Fram Strait, Eurasian Basin, East Greenland Current and Denmark Strait overflow. These studies are summarised in the present paper. It has been estimated that 22% of the 137Cs Sellafield discharge has passed into the Barents Sea, en route to the Nansen Basin, via the Bjomoya-Fugloya Section, with another 13% passing through the Fram Strait. This amounts to 14 PBq 137Cs. Quantifying the influx of other radionuclides has been more problematic. The inflowing Atlantic water now appears to be diluting waters in the Arctic Basin, which were contaminated in the late 1970s and early 1980s as a result of the substantial decrease in the discharge of reprocessing wastes. Sellafield (U.K.) has dominated the supply of 134Cs, 137Cs, 90Sr, 99Tc and Pu, whereas La Hague (France) has contributed a larger proportion of 129I and 125Sb. 相似文献
9.
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
10.
Hideyuki Kawamura Toshimichi Ito Takuya Kobayashi Shigeyoshi Otosaka Naoki Hirose Orihiko Togawa 《Journal of Oceanography》2010,66(5):649-662
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
11.
良好的环境质量是厦门成为一个宜居和滨海旅游城市的重要基石。自日本福岛核事故发生和福建省核电站陆续运行之后,厦门邻近海域潜在的核污染风险受到公众和管理部门的关注。本研究测定了2015年2月和8月厦门邻近海域海水和海洋沉积物中主要放射性核素的含量水平,并据此评价了该海域的环境放射性质量状况。结果表明海水中总铀、90Sr、226Ra、137Cs处于我国海洋放射性水平变化范围以内,无明显季节差异,其他放射性核素58Co、60Co、134Cs、110mAg、59Fe、54Mn、65Zn均未检出,海水中90Sr和137Cs的活度最大值远低于国家海水水质标准限值,海洋沉积物中放射性核素活度水平亦在我国海洋放射性水平变化范围以内。利用我国现有的海洋放射性环境质量评价方法对厦门邻近海域放射性质量状况进行分级评价得出其海水放射性质量为2级,海洋沉积物放射性环境质量为1级,均属于安全级别。研究结果表明2015年在厦门附近海域未观测到放射性污染现象。 相似文献
12.
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
13.
D. Knapinska-Skiba R. Bojanowski Z. Radecki G. E. Millward 《Estuarine, Coastal and Shelf Science》2001,53(6):779
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
14.
90Sr长期被视为最重要的人工放射性核素之一，日本福岛核事故导致包括90Sr在内的大量放射性物质泄漏进入海洋，厂区储水罐中冷却废水至今仍然存在大量90Sr。海洋中90Sr分析方法却繁琐耗时，导致核事故后的90Sr研究较为匮乏，且缺乏系统的认识。本研究在2015?2018年期间测量南海海水和多种海洋生物(马尾藻、海虾、牡蛎、红树林植物、造礁珊瑚)中90Sr的基础上，深入分析核事故后日本周边海域和南海90Sr的比活度水平与环境半衰期。结合文献资料，本研究发现1975?2010年期间日本近岸海水90Sr的环境半衰期为15.4 a，2011年的核事故后日本周边海洋中90Sr比活度显著升高，基于ERICA软件定量计算核事故后90Sr对海洋鱼类的剂量率比核事故前的结果高5个数量级。南海作为福岛核事故后北太平洋环流的下游海域，本文进一步构建1984?2018年期间南海90Sr比活度的历史曲线，发现核事故前后南海90Sr比活度水平没有可识别的变化，进一步定量计算南海90Sr的环境半衰期为26.7 a，发现边缘海和大洋中90Sr和137Cs环境半衰期格局差异与核素(90Sr和137Cs)的源汇过程(河流输入和海洋生物泵)密切相关。鉴于海洋中90Sr分析方法的挑战性，本文发现在10多种海洋生物中造礁珊瑚骨骼几乎拥有最高的90Sr浓集因子(约1 000 L/kg)，同时具有较易大量获取、固定附着生长、连续高分辨率记录、前处理简单快速等优点，很可能是海洋中90Sr可靠的指示生物。造礁珊瑚中90Sr研究将有利于揭示人工放射性核素的源汇过程，同时为我国海洋放射性监测方案和相关标准导则的优化和完善提供有益的参考。 相似文献
15.
Sang-Han Lee Pavel P. Povinec Janine Gastaud Beniamino Oregioni Laurent Coppola Catherine Jeandel 《Journal of Oceanography》2009,65(3):397-406
Anthropogenic 90Sr, 239,240Pu and 241Am were used as tracers of water mass circulation in the Crozet Basin of the South Indian Ocean, represented by three main
water fronts—Agulhas (AF), Subtropical (STF) and Subantarctic (SAF). Higher 90Sr concentrations observed north of 43°S were due to the influence of AF and STF, which are associated with the south branch
of the Subtropical gyre, which acts as a reservoir of radionuclides transported from the North to the South Indian Ocean.
On the other hand, the region south of 43°S has been influenced by SAF, bringing to the Crozet Basin Antarctic waters with
lower radionuclide concentrations. The 238Pu/239,240Pu activity ratios observed in water and zooplankton samples indicated that, even 35 years after the injection of 238Pu to the Indian Ocean from the burn-up of the SNAP-9A satellite, the increased levels of 238Pu in surface water and zooplankton are still well visible. The radionuclide concentrations in seawater and their availability
to zooplankton are responsible for the observed 210Po, 239,240Pu and 241Am levels in zooplankton. 相似文献
16.
Interaction of 54Mn and 55(59)Fe with EDTA in seawater and NaCl solutions was investigated by high-voltage paper electrophoresis. These two radionuclides were chosen because they represent two modes of behaviour of radionuclides in seawater—EDTA systems. In seawater without EDTA or at low EDTA concentrations in the systems 54Mn behaves as a cation while 55(59)Fe gives a zone at the starting point of the electrophoretic strip. At higher EDTA concentrations, both radionuclides give only one anionic zone showing complexing with EDTA. In the intermediate range of the EDTA concentration (“transition region”) 54Mn shows continuous change of the electrophoretic mobility from cationic to anionic (fast rate of interaction with EDTA), while 55(59)Fe reacts very slowly giving two well-separated zones in the transition region of the EDTA concentration.EDTA concentrations were varied from 10?6 to 10?2M, pH being adjusted to 8.0. The behaviour of radionuclides was followed by measuring the electrophoretic mobilities of radionuclides in dependence on the EDTA concentration at different aging times from 0 to 7 days.From the experimental data effective stability constants and the number of EDTA-ligands of 54MnEDTA and 55(59)FeEDTA complexes in seawater and 0.55 M NaCl solutions were calculated. 相似文献
17.
Further studies on the transport in sea water and accumulation in marine sediment of the radionuclides, released from a nuclear power plant, on Urazoko Bay, Fukui Prefecture were reported.The partition of radionuclides among the particle size fractions of a sediment sample indicated that the accumulation of60Co,137Cs and54Mn in the sediment were dominated substantially by the sorption on the particle surface in sea water, and the patterns of their sorption were considerably similar to each other.In regard to the60Co contamination of marine sediments in an area of about 13 km2 around the nuclear power plant, 60% of the60Co contamination were retained in Urazoko Bay, which occupies only 7% of the bottom surface of the region.It is clear that a part of60Co accumulated in the sediment of Urazoko Bay gradually moved to the outerward. 相似文献
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历次核试验进入海洋的~(137)Cs对中国近海影响的模拟研究 总被引：1，自引：0，他引：1
1945年以来,世界各主要核国家进行了数千次核试验,这些核试验产生的绝大部分放射性物质通过多种途径进入海洋,对海洋环境造成放射性污染。本文建立了一个准全球海洋的放射性物质输运和扩散数值模式,通过数值模拟手段评估了历史核试验释放的放射性物质137 Cs对中国近海海洋环境的影响。本文借助前人工作评估了核试验释放137Cs进入海洋的途径和总量;通过比较模拟结果与观测资料,表明本文建立的放射性物质模式能够较好地模拟出137Cs在中国近海及其邻近海域的分布情况和随时间演变特征;模拟结果表明中国近海里的137Cs浓度在20世纪50年代中期达到最大,其中吕宋海峡海域137Cs浓度最高,达80.99Bq/m3;进一步分析了2011年3月份日本福岛核事故前中国近海137Cs浓度分布状况,2011年整个中国近海137Cs浓度介于1.0~1.6Bq/m3间,且其浓度垂向分布较均匀,相对封闭的南海浓度略高于其他海域。 相似文献