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1.
Nuclide-specific activity and sediment grain size were analyzed at locations along the North Branch of the Yangtze (Changjiang) Estuary. The spatial distributions of various radioisotopes are presented, along with the sources and applications of these nuclides for studies of the aquatic environment. The specific activities of sediment radionuclides in the North Branch increase toward the ocean, indicating that the sediment is transported from the downstream side of the estuary into the North Branch. The 226Ra/228Ra ratio agrees well with the observed results and can be used to identify trends in erosion and accretion in the North Branch.  相似文献   

2.
One hundred and twenty one samples from every major plutonic body (mainly granitic) of Greece have been analyzed by γ-ray spectrometry to determine the specific activities of 238U, 232Th and 40K (Bq/kg). The range of the activity concentrations of these radionuclides was 2.3–266.4, 1.8–375.5 and 55.0–1632.0 Bq/kg and their average values were 79.2, 85.3 and 881.4 Bq/kg respectively. Any possible connection between the specific activities of 238U, 232Th and 40K and some characteristics of the studied samples (age, rock-type, colour, grain-size, occurrence and chemical composition) is investigated. Samples of particular colour, rock-type, occurrence and chemical composition have been identified for their distinctive levels of natural radioactivity, while age and grain-size do not affect the concentrations of 238U, 232Th and 40K. The range of the Th/U ratio was 0.7–12.69. This great variation in the Th/U ratios, especially when it is found among the samples of the same pluton, is also discussed and explained by alteration and tectonic–metamorphic processes.  相似文献   

3.
Natural radioactivity in sediment of Wei River,China   总被引：1，自引：0，他引：1  
The concentrations of natural radionuclides in sediment of Wei River of China were measured using γ-ray spectrometry with the aim of estimating the radiation hazard as establishing a database for radioactivity levels of river sediment of China. The activity concentrations of 226Ra, 232Th and 40K in sediment samples ranged from 10.4 to 39.9 Bq kg−1, 15.3 to 54.8 Bq kg−1 and 514.8 to 1,175.5 Bq kg−1, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities of Chinese soil and Shaanxi soil. Radium equivalent activity (Raeq), external hazard index (H ex) and representative level index (I γr) were calculated for the samples to assess the radiation hazards arising due to the use of these sediment samples in the construction of dwellings. All the sediment samples have Raeq lower than the limit of 370 Bq kg−1, H ex less than unity and I γr close to 1 Bq kg−1. The overall mean outdoor terrestrial gamma dose rate is 64.8 nGy h−1 and the corresponding outdoor annual effective dose is 0.079 mSv. None of the studied location is considered a radiological risk and sediment can be safely used in construction.  相似文献   

4.
This study centers on the question: How sensitive are 231Pa/230Th and 10Be/230Th to sediment composition and redistribution? The natural radionuclides 231Pa, 230Th and 10Be recorded in deep sea sediments are tracers for water mass advection and particle fluxes. We investigate the influence of oceanic particle composition on the element adsorption in order to improve our understanding of sedimentary isotope records. We present new data on particle size specific 231Pa and 10Be concentrations. An additional separation step, based on settling velocities, led to the isolation of a very opal-rich phase. We find that opal-rich particles contain the highest 231Pa and 10Be concentrations, and higher 231Pa/230Th and 10Be/230Th isotope ratios than opal-poor particles. The fractionation relative to 230Th induced by the adsorption to opal-rich particles is more pronounced for 231Pa than for 10Be. We conclude that bulk 231Pa/230Th in Southern Ocean sediments is most suitable as a proxy for past opal fluxes. The comparison between two neighboring cores with rapid and slow accumulation rates reveals that these isotope ratios are not influenced significantly by the intensity of sediment focusing at these two study sites. However, a simulation shows that particle sorting by selective removal of sediment (winnowing) could change the isotope ratios. Consequently, 231Pa/230Th should not be used as paleocirculation proxy in cases where a strong loss of opal-rich material due to bottom currents occurred.  相似文献   

5.
The adsorption rate constants of Ra and Th were estimated from empirical data from a freshwater lake and its feeding saline springs. We utilized the unique setting of Lake Kinneret (Sea of Galilee, northern Israel) in which most of the Ra and Th nuclides are introduced into the lake by saline springs with high 226Ra activities and a high 224Ra/228Ra ratio of 1.5. The mixing of the Ra enriched saline waters and freshwater in the lake causes the 224Ra/228Ra ratio to drop down to 0.1 in the Kinneret due to preferential adsorption of 228Th. These conditions constitute a “natural experiment” for estimating adsorption rates. We developed a simple mass-balance model for the radionuclides in Lake Kinneret that accurately predicted the Ra isotope ratios and the 226Ra activity in the lake. The model is comprised of simultaneous equations; one for each radionuclide. The equations have one input term: supply of radionuclides from the saline springs; and three output terms: adsorption on particles in the lake, radioactive decay and outflow from the lake. The redundancy in the analytical solutions to the mass balance equations for the relevant nuclides constrained the values of Ra and Th adsorption rate constants to a very narrow range. Our results indicate that the adsorption rate constant for Ra is between 0.005 d−1 and 0.02 d−1. The rate constant for Th is between 0.5 d−1 and 1 d−1, about fifty to a hundred times higher. The estimated desorption rate coefficient for Ra is about 50-100 times larger than its adsorption rate constant. The mass-balance equations show that the residence times of all Ra isotopes (226Ra, 228Ra,223Ra, 224Ra) and of 228Th in the lake are about 95, 92, 14, 6 and 1 d, respectively. These residence times are much shorter than the residence time of water in the lake (about 5.5 y). The steady state activity ratios in Lake Kinneret depend mainly on the adsorption rate constants, decay constants, the outflow rate from the lake and the activity ratios in the saline springs. The activity ratios are independent of the saline springs flow rate.  相似文献   

6.
The study referred to measure activity concentrations of some primordial radionuclides and anthropogenic of 137Cs in soil samples of Mami-water in the Menoua subdivision, Dschang employing gamma-ray spectrometry-based characterized Broad Energy Germanium (BE6350) detector and a comparison of radiological and safety impact parameters on human due to primordial radioactivity in soil with some internationally approved values. In addition, statistical analysis of primordial radionuclides of 226Ra, 232Th and 40K was performed to evaluate the distribution and the interrelation of radionuclides. Samples were randomly collected from a depth of about 0 to 5 cm from the top surface layer. Each of the sampling points was considered as being overlaid with a grid and subdivided into cells. The observed radioactivity level of 226Ra, 232Th and 40K in the investigated soil samples was compared with some published data available in some countries including Cameroon and observed varying within some reported data of radioactivity in soil from bauxite ore deposit. 235U and 137Cs were found in very few samples with a very low average of activity concentrations. In the majority of the samples, the observed radiological safety parameters seem to be greater than the internationally approved values. Consequently, using bricks made of soil as building materials might lead to an increase in radiation risk for the population. Multivariate statistical analysis of activity concentrations of primordial radionuclides performed showed an asymmetrical distribution with more peaked than Gaussian distribution and relatively flatter distribution of radionuclides in soil. In addition, a good positive interrelation between 226Ra and 232Th was observed and a weak negative one observed between 40K and 226Ra–232Th.  相似文献   

7.
Cesium and Strontium concentrations were analyzed in eight pedogenetic soil profiles developed on different rocks from a semiarid mediterranean region: La Mancha (Central Spain). Concentration activities of 137Cs and 90Sr, as for some soil properties, were also measured. The results are presented in this document: Cs concentrations range between 0.4 and 18.3 mg kg−1 and Sr varies widely between 11.0 and 3,384 mg kg−1. Therefore, it is clear that there is a broad range of concentrations and there are also values significantly higher than the average values stated by several authors. Concentrations of long-life artificial radionuclides (137Cs, 90Sr) were determined in some of the same soils. The activity concentration mean values (Bq kg−1) were ranging between 0.82 and 21.76 for 137Cs and 90Sr variations range between 6.73 and 0.35. There were no significant correlations between radionuclides and stable trace elements. The data indicate that the soils do not show significant radioactivity of these elements and therefore they do not pose a danger. By the same token, no risk of contamination by this activity was detected. Finally, spatial patterns seem to be affected by the soil type and some soil properties.  相似文献   

8.
The concentrations and distribution of natural and artificial radionuclides in sediment and water samples collected from Fırtına River in the Eastern Black Sea region of Turkey were investigated with an aim of evaluating the environmental radioactivity and radiation hazard. Natural gross α and gross β activities were determined for 21 different water samples, and the activity concentrations were obtained for 226Ra, 214Pb, 214Bi, 228Ac, 208Tl, 40K and 137Cs in 20 different sediment samples. The obtained results showed that natural gross α and gross β activity concentrations in water samples range from 12.4 ± 3.4 to 66.2 ± 9.2 mBq l−1 and from 27.9 ± 3.3 to 133.3 ± 4.1 mBq l−1, respectively. The mean activity concentrations were 32.6 ± 3.8 mBq l−1 for gross α and 69.9 ± 4.4 mBq l−1 for gross β. Generally, the gross β activities were higher than the corresponding gross α activities. The average concentrations of 238U and 232Th daughter products vary from 11 to 167 Bq kg−1 and from 16 to 107 Bq kg−1, respectively. The concentrations of 40K and 137Cs vary from 51 to 1,605 Bq kg−1 and from 0.8 to 42 Bq kg−1, respectively. Sediment characterization was also investigated using grain size, thin section and XRD analysis.  相似文献   

9.
South India is one of the regions in the world that has the highest background radiation levels. In this region, river sediments are used in large quantities as building material. Therefore, the knowledge of the radionuclides distribution in such sediments is important for assessing their potential adverse effects on humans residing in buildings made of sediment material. For this goal, we focus on the determination of the natural radioactivity levels and magnetic properties in sediment samples collected from 33 locations along the southwestern Bharathapuzha river originating from the Anamalai hills. The sediment samples were subdivided into two categories according to particle size. It is observed that the average activity concentrations of 226Ra, 232Th, and 40K in sediment samples varied greatly with granulometric and geological differences. The average values of 226Ra, 232Th, and 40K and its associated radiological hazard parameters for category II samples (particle size between 149 μm and 2 mm) were lower than category I sediment samples (bulk samples). Moreover, the average radionuclide activity concentrations (except for 40K) and the calculated radiation hazard parameters are higher in the lowland region compared to the highland and the midland regions. The mass-specific magnetic susceptibility values ranged widely along the river, as well as between physiographic regions, e.g., average values for category I sediment samples were 950.2 × 10?8, 351.1 × 10?8 and 131.8 × 10?8 m3 kg?1 (for high-, mid- and lowland regions, respectively). Differences between physiographic regions and sediment fractions from both radioactivity determinations and magnetic parameters were analyzed with statistical tests and multivariate analysis, which showed the advantages of using both independent techniques.  相似文献   

10.
In this study, activity concentrations of 40K, 226Ra and 232Th in fertilized soil samples and different organic and inorganic fertilizers used in agricultural soil were analysed using gamma-ray spectrometry NaI (Tl) detector in order to access the implications of extended use of fertilizers in 2–3 years. The concentrations of radionuclides in some granular fertilizer brands were discovered to be higher for 40K, 226Ra and 232Th than those obtained in leafy fertilizer, animal fertilizer and fertilized soil samples. From the results, the highest overall mean concentrations of the specific activities of 40K, 226Ra and 232Th were 2301.8 (granular fertilizer), 42.5 (leafy fertilizer) and 327.1 (animal fertilizer) in Bq kg?1, while the lowest values observed in the specific activities of the same radionuclides were 357.7 (leafy fertilizer), 28.1 (animal fertilizer) and 36.5 (animal fertilizer). The radiological hazards of the radium equivalent (Raeq), normative value (NRN), outdoor radium equivalent (Raeq-out), external hazard index (H ext), internal hazard index (H in), dose rate, annual effective dose rate, activity utilization index and concentration accumulation index (CAI) and RaFZ due to the presence of these radionuclides in the investigated samples were calculated. Nevertheless, some of the fertilizer brands have higher concentration values than the recommended limit, and the values of hazard indices of fertilizer brands used in the selected teaching and research farms were within acceptable limit. Therefore, the fertilized soil samples in the studied farms are safe.  相似文献   

11.
The objective of this study was chemical and radiological characterization of Kastela Bay sediments exposed to numerous anthropogenic sources like deposition of fly and bottom ash enriched in radionuclides and heavy metals, chemical plant, cement plant, iron plant, shipyard, electroplating facility, untreated industrial and domestic waste waters as well as heavy traffic. Totally, 33 samples of the mixture of fly and bottom ash, 12 sediment cores ranging from 0 to 40 cm and nine surface sediment samples were analyzed. Enrichment in heavy metals in the mixture of fly and bottom ash was ranging from 1.5 to 36 times compared to flysch soil while 226Ra and 238U were up to 50 times enriched compared to average activities characteristic for surrounding soils developed on the Middle and Upper Eocene flysch. Maximum 238U activity was approximately 32 times higher and 226Ra approximately 40 times higher in the Kastela Bay sediment compared to mean value determined for Adriatic sediments. The highest enrichment in sediment cores compared to background values were found for Zn (35.6 times), Pb (16 times), Cr (9.1 times) and Ni (4 times)  相似文献   

12.
Several water and surface microlayer samples from Lake St. Clair, the Niagara River, and the North Shore of Lake Ontario collected during 1983–1986 have been assayed for a variety of radionuclides. In addition, the foam accumulating in the pool just below Niagara Falls was also analyzed and found to be the most efficient aqueous phase collector of137Cs,210Pb, and226Ra.The order of radioisotope specific activities from highest to lowest is: Lake Ontario sediment, Niagara River suspended solids, Niagara River foam, surface microlayer water, and subsurface water. Radiological dose rates to the sediments from137Cs,226Ra, and228Th total about 5 mGy/y.  相似文献   

13.
This paper presents a detailed survey of the activities of selected man-made radionuclides in peat deposits located in SW Spitsbergen. Peat cores from the High Arctic (SW Spitsbergen) were analyzed by gamma spectrometry (137Cs), alpha spectrometry (238Pu, 239,240Pu, 241Am activities) and by ICPMS (240Pu/239Pu atom ratios). Maximum activities evident in the peats correspond to the 1963/1964 global maximum fallout from atmospheric testing of nuclear weapons; some of the activity profiles have been altered post-deposition by water infiltration. Activity ratios of 238Pu/239+240Pu, 241Am/239+240Pu, 239+240Pu/137Cs and 240Pu/239Pu atom ratios indicate mixing between global (stratospheric) and regional (tropospheric) sources of these radionuclides in the Svalbard area. The 238Pu/239+240Pu activity ratios varied from 0.02 ± 0.01 to 0.09 ± 0.03, suggesting global fallout as the dominant source of Pu. The 239+240Pu/137Cs activity ratios varied from 0.01 ± 0.01 to 0.42 ± 0.11, which apparently arises from the post-depositional mobility of 137Cs. The 241Am/239+240Pu activity ratios ranged between 0.10 ± 0.02 and 1.5 ± 0.3 and exceed the published global fallout ratio for Svalbard of 0.37 due to the relatively higher geochemical mobility of Pu vs. Am and/or ingrowth of Am from the decay of 241Pu. The atom ratio 240Pu/239Pu ranged from 0.142 ± 0.006 to 0.241 ± 0.027; however, the vast majority of peat samples exhibited 240Pu/239Pu atom ratios similar to the stratospheric fallout (∼0.18).  相似文献   

14.
Multiple sediment cores were collected in June 1994 in the turbidity maximum zone of the Hudson River estuary off Manhattan, New York. Results from X-radiography of the sediments and measurements of natural radionuclides (234Th,7Be, and210Pb) and trace metals (Ag, Cd, Cu, Pb, and Zn) show significant spatial variability of sediment composition and structure and patchy distributions of radionuclides activities and trace metal concentrations in this small area (0.6 km × 0.5 km). Radionuclide and trace metal analyses confirm prior work (Olsen et al. 1978; Olsen et al. 1981; Hirschberg et al. 1996) that show the western margin area of the river acts as a repository of these chemical constituents at least for the short-term period (0.5–1 yr), and the mid-channel area is not a depositional area for sediments and associated chemical constituents.7Be profiles reveal short-term sediment deposition rates ranging from 6 cm yr?1 to 26 cm yr?1 in the western margin area. Significant spatial variations in excess234Th and7Be inventories (up to a factor of 10 and 5 for234Th and7Be, respectively) are found in the western margin depositional area, although the inventories are balanced, on average, with in situ production in water column and atmospheric supply. The spatial variation of surficial excess210Pb and trace metal concentrations in depositional areas of the western margin are ≤10% for Ag, Cu, Pb, and Zn and 29% for Cd. However, the variations in the transition zone range from 28% to 93%. This variability is likely related to variations in tidal current velocity, bottom shear stress, and river channel morphology.  相似文献   

15.
U-series disequilibria measured in waters and rocks from a chalk aquifer in France have been used as an analog for long-term radionuclide migration. Drill core samples from a range of depths in the vadose zone and in the saturated zone, as well as groundwater samples were analyzed for 238U, 234U, 232Th and 230Th to determine transport mechanisms at the water/rock interface and to quantify parameters controlling the migration of radionuclides. Isotope measurements in rocks were done by TIMS, whereas (234U/238U) and (230Th/232Th) activity ratios in water samples were measured by multi-collector-ICP-MS. Both depletion and enrichment in 234U relative to 238U were observed in carbonate rock samples resulting from chemical weathering in the unsaturated zone and calcite precipitation in the zone of water-table oscillation, respectively. The correlation between (230Th/232Th) activity ratios and 87Sr/86Sr ratios found in the chalk samples indicates that thorium is mainly contained in a minor silicate phase whose abundance is variable in chalk samples. Water samples are all characterized by (234U/238U) > 1 resulting from α-recoil effect of 234Th. Groundwaters are characterized by a more radiogenic signature in 87Sr/86Sr than the rocks. Moreover, (230Th/232Th) activity ratios in the waters are lower than in the rocks, and increase with distance from the water divide, which suggests that Th transport is controlled by colloids formed during water infiltration in the soil. A 1-D transport model has been developed in order to constrain the U-series nuclide transport considering a transient behavior of radionuclides in the aquifer and a time-dependent composition for the solid phase. This model permits a prediction of the time scale of equilibration of the system, and an estimation of parameters such as weathering rate, distribution coefficients and α-recoil fractions. Retardation factors of 10-35 and from 1 × 104 to 2 × 105 were predicted for U and Th, respectively, and can be used to predict the migration of radionuclides released as contaminants in the environment. At the scale of our watershed (∼32 km2), a characteristic migration time from recharge to riverine discharge of 200-600 yr for U and 0.2-3.7 Myr for Th was obtained.  相似文献   

16.
The activities of the most common, naturally occurring radionuclides 238U, 226Ra, 210Pb, 228Ra, 228Th, and 40K were measured by gamma-ray spectrometry in samples from reservoir rocks, geothermal fluids, and mineral precipitates at the geothermal research site Groß Schönebeck (North German Basin). Results demonstrated that the specific activity of the reservoir rock is within the range of the mean concentration in the upper earth crust of <800 Bq/kg for 40K and <60 Bq/kg for radionuclides of the 238U and 232Th series, respectively. The geothermal fluid showed elevated activity concentrations (up to 100 Bq/l) for 226Ra, 210Pb, and 228Ra, as compared to concentrations found in natural groundwater. Their concentration in filter residues even increased up to 100 Bq/g. These residues contain predominantly two different mineral phases: a Sr-rich barite (Sr, BaSO4) and laurionite (PbOHCl), which both precipitate upon cooling from the geothermal fluid. Thereby they presumably enrich the radionuclides of Ra (by substitution of Ba) and Pb. Analysis of these precipitates further showed an increased 226Ra/228Ra ratio from around 1–1.7 during the initial months of fluid production indicating a change in fluid composition over time which can be explained by different contributions of stimulated reservoir rock areas to the overall produced fluid.  相似文献   

17.
The collection of large volumes of pore water (1–2 liters per 2 cm horizon of sediment) and low level radiochemical measurements of 239,240Pu and 137Cs have been combined to produce the first study of these fallout artificial radionuclides in marine pore waters. Profiles from box cores taken in June and September 1982 from Buzzards Bay, Mass., are reported along with profiles of many diagenetic constituents (i.e. SO42?, alkalinity, Fe, Mn, DOC, and nutrients).The 239,240Pu pore water profile is characterized by a subsurface maximum of about 0.28 dpm/100 kg lying between 3–11 cm. Overlying seawater, in contrast, has an activity of 0.01 ± 0.02 dpm/100 kg. Below about 11 cm, the pore water 239,240Pu distribution follows that of the solid phase which decreases rapidly with depth. The pore water profiles of 137Cs are characterized by a broad and deeply penetrating maximum where activities of about 35–40 dpm/100 kg extend from 3 to 20 cm. Overlying seawater, in contrast, has an activity of 17–24 dpm/100 kg. The 137Cs and 239,240Pu pore water data show that there is preferential downward transport of 137Cs and that 239,240Pu does not have an active diagenetic chemistry and is not significantly mobile in these coastal sediments.  相似文献   

18.
This study of environmental radioactivity was carried out in the soils of an urban area. Naturally occurring gamma-emitting radionuclides and man-made 137Cs were found in the soil profiles collected from four parks in the central Belgrade city area and the soil layer was examined every 10 cm and to a depth of 50 cm. Radioisotope activity concentrations (Bq kg?1) in the samples of urban soil using the gamma-ray spectrometry method were in the range of 14–46 for 238U, 33–50 for 226Ra, 29–63 for 210Pb, 1.2–3.4 for 235U, 28–50 for 232Th, 424–576 for 40K and 0.7–35.8 for 137Cs. Some of the basic physicochemical soil properties (pH, organic matter content, calcium-carbonate content, particle size distribution) were determined to investigate the impact on the vertical distribution of radionuclides. The results of this investigation showed that variations of activity concentration ratios of radionuclides that belong to the same (238U/226Ra) or different radioactive series (232Th/226Ra; 235U/238U), including 210Pb/137Cs ratios could well be explained by the properties of the soil. Alkaline pH reaction, the accumulation of organic matter in the uppermost and of carbonates in the deepest layers of urban soil had an effect on 238U/226Ra, and 210Pb/137Cs activity concentration ratio values, while 232Th/226Ra and partially 235U/238U ratios were associated with the particle sizes vertical distribution. A study of radionuclides in the samples of leaves of two deciduous tree species common for these parks was also conducted and 210Pb and 40K were found concentrated in leaves rather than other investigated radionuclides.  相似文献   

19.
《Chemical Geology》2002,182(2-4):409-421
An improved method was developed to measure 226Ra, 228Ra and 224Ra in freshwaters by gamma spectrometry. Radium was selectively extracted from acidified samples using specific filters (3M EMPORE™ Radium Rad disks). The latter was subsequently analysed by gamma spectrometry. Simultaneous and direct determination of the activities of the three isotopes was performed by comparison of gamma rays of the Radium Rad disks with those of a calibrated standard disk. This efficient and reliable method allowed a reduction of sample processing to a few hours.This technique was applied to analyse the Ra isotope compositions of several CO2-rich hydrothermal springs of the western border of the Limagne graben (French Massif Central). The studied springs emerge from a succession of granitic outcrops lined up along a major fault. Their chemical compositions evolve from calcic and magnesian chloro-bicarbonated to sodic bicarbonated. All the springs display high Ra activities, probably linked to high CO2 content and/or high cation content of these waters, with various Ra isotope ratios. 226Ra activity ranges from 588 to 2287 mBq/l and 228Ra activity from 260 to 1590 mBq/l, whereas 224Ra displays an activity between 245 and 1808 mBq/l. Four of the six analysed springs have (228Ra/226Ra) activity ratios lower than 0.7, thus, significantly lower than the ratio expected from an interaction with a calc-alkaline granitoid (typically having (232Th/238U) activity ratio between 1 and 2). Low (228Ra/226Ra) ratio (0.27) of the northern water (Montpensier) suggests the existence in this area of a zone of U concentration, possibly resulting from U mobilization and accumulation induced by previous hydrothermal events. The (224Ra/228Ra) ratios display smaller variations. They suggest short transit times from the zone of Ra leaching to the surface (a few days) or a very shallow addition of 224Ra (e.g., from a localised zone where 228Th could be preferentially adsorbed on the mineral surfaces). In some cases, these ratios might be used to infer differences in transit times of waters between neighboring springs.  相似文献   

20.
Field experiments and laboratory studies were performed to investigate migration processes of plutonium isotopes from a near-surface radioactive waste trench to the underlying sandy aquifer at the Red Forest waste dump in the Chernobyl zone. The objectives of these experiments were to characterize the spatial distribution and possible migration mechanisms of plutonium in the aquifer. During 2002–2007 experimental investigations were carried out and spatial distributions of plutonium isotopes (239,240Pu, 238Pu), 90Sr and major ions in the aquifer in the direction of the groundwater flow were obtained. Specific activities of radionuclides in groundwater depended on the location of the piezometer and varied in the range of 1–360 mBq kg−1 for 239,240Pu, 0.5–180 mBq kg−1 for 238Pu and n–n·104 Bq kg−1 for 90Sr. It was found that the spatial features of the distributions of plutonium and strontium specific activities in the upper eolian aquifer were similar, i.e. there was a correlation between the positions of the activity maxima of the radionuclides. The Pu isotopes plume in the aquifer spreads about 15 m downstream of the radionuclides source. Characterization of the initial radionuclide composition of the waste showed that all plutonium in the aquifer originated from the trench. The ratio of plutonium isotopes (239,240Pu/238Pu) at the sampling time was the same in waste material and in groundwater samples. In situ ultrafiltration of several groundwater samples was carried out. The size fractionation data obtained suggest that a significant part of plutonium (50–98%) in the groundwater sampled close to the source from the upper part of the aquifer is associated with a very low molecular weight fraction (<1 kDa).  相似文献   

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