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1.
《Applied Geochemistry》1993,8(5):447-471
Ground water is the main source of domestic and public supply in the Carson River Basin. Ground water originates as precipitation primarily in the Sierra Nevada in the western part of Carson and Eagle Valleys, and flows down gradient in the direction of the Carson River through Dayton and Churchill Valleys to a terminal sink in the Carson Desert. Because radionuclides dissolved in ground water can pose a threat to human health, the distribution and sources of several naturally occurring radionuclides that contribute to gross-alpha and gross-beta activities in the study area were investigated. Generally, alpha and beta activities and U concentration increase from the up-gradient to down-gradient hydrographic areas of the Carson River Basin, whereas222Rn concentration decreases. Both226Ra and228Ra concentrations are similar throughout the study area. Alpha and beta activities and U concentration commonly exceed 100 pCi/l in the Carson Desert at the distal end of the flow system. Radon-222 commonly exceeds 2,000 pCi/l in the western part of Carson and Eagle Valleys adjacent to the Sierra Nevada. Radium-226 and228Ra concentrations are <5pCi/l. Four ground water samples were analyzed for210Po and one sample contained a high concentration of 21 pCi/l. Seven samples were analyzed for210Pb; six contained <3pCi/l and one contained 12 pCi/l. Thorium-230 was detected at concentrations of 0.15 and 0.20 pCi/l in two of four samples.Alpha-emitting radionuclides in the ground water originated from the dissolution of U-rich granitic rocks in the Sierra Nevada by CO2, oxygenated water. Dissolution of primary minerals, mainly titanite (sphene) in the granitic rocks, releases U to the water. Dissolved U is probably removed from the water by adsorption on Fe- and Mn-oxide coatings on fracture surfaces and fine-grained sediment, by adsorption on organic matter, and by coprecipitation with Fe and Mn oxides. These coated sediments are transported throughout the basin by fluvial processes. Thus, U is transported as dissolved and adsorbed species. A rise in the water table in the Carson Desert because of irrigation has resulted in the oxidation of U-rich organic matter and dissolution of U-bearing coatings on sediments, producing unusually high U concentration in the ground water.Alpha activity in the ground water is almost entirely from the decay of U dissolved in the water. Beta activity in ground water samples is primarily from the decay of40K dissolved in the water and ingrowth of238U progeny in the sample before analysis. Approximately one-half of the measured beta activity may not be present in ground water in the aquifer, but instead is produced in the sample after collection and before analysis. Potassium-40 is primarily from the dissolution of K-containing minerals, probably K-feldspar and biotite. Radon-222 is primarily from the decay of226Ra in the aquifer materials. Radium in the ground water is thought to be mainly from alpha recoil associated with the decay of Th in the aquifer material. Some Ra may be from dissolution (or desorption) or Ra-rich coatings on sediments.  相似文献   

2.
228Ra, 226Ra, and 222Rn activities were determined on over 150 ground water samples collected from drilled, public water supply wells throughout South Carolina. A wide range of aquifer lithologies were sampled including the crystalline rocks of the Piedmont and sedimentary deposits of the Coastal Plain. A significant linear relationship between log 228Ra and log 226Ra (n = 182, r = 0.83) was indistinguishable between Piedmont and Coastal Plain ground water. Median 228Ra226Ra activity ratios for the Piedmont, 1.2, and Coastal Plain, 1.3, ground water are close to estimated average crustal 232Th238U activity ratios of 1.2 to 1.5 corresponding to Th/U weight ratios of 3.5 to 4.5. A linear correlation was also found between log 222Rn and log 226Ra for Piedmont (n = 68, r = 0.62) and Coastal Plain (n = 89, r = 0.64) ground water. However, the median 222Rn226Ra activity ratio for Piedmont ground water, 6100, was much higher than for Coastal Plain ground water, 230. Higher excess 222Rn activities may be due to greater retention of 226Ra by the chemically active Piedmont aquifers compared to the more inert sand aquifers sampled in the Coastal Plain. The relationship between log 228Ra and log 226Ra was used to predict total Ra (228Ra + 226Ra) distributions in Appalachian and Atlantic and Gulf Coastal Plain ground water. Predictions estimate that 2.4% of Appalachian and 5.3% of Atlantic and Gulf Coastal Plain ground water supplies contain total Ra activities in excess of the 5 pCi/l limit established by the U.S. Environmental Protection Agency. These predictions also indicate that 40–50% of these ground water wells may be overlooked using the presently suggested screening activity of 3.0 pCi/l of 226Ra for 228Ra analysis.  相似文献   

3.
?The gross beta and 228Ra radioactivity measurements in mineral waters were performed by proportional counter and gamma spectrometry, respectively, in this study. The natural mineral water samples were collected from various regions of Turkey for this study. Gross beta activities have been determined according to the United States Environmental Protection Agency standard method (EPA 900). In the case that the gross beta activity was determined to be greater than 1 Bq/L, then the 228Ra activity concentration in the related mineral water sample was specifically measured. 228Ra activity in mineral water samples was determined by high-purity germanium (HPGe) detector. The photopeak efficiencies were calculated by modeling the sample geometry and the detector in Canberra software LabSOCS. The gross beta activities in the eight of 32 bottled mineral water samples were greater than 1 Bq/L. 228Ra activity concentrations in bottled mineral waters were determined within 0.100–1.04 Bq/L. The committed effective doses were calculated for three different scenarios according to mineral water consumption rates.  相似文献   

4.
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   

5.
A total of 1270 raw-water samples (before treatment) were collected from 15 principal and other major aquifer systems (PAs) used for drinking water in 45 states in all major physiographic provinces of the USA and analyzed for concentrations of the Ra isotopes 224Ra, 226Ra and 228Ra establishing the framework for evaluating Ra occurrence. The US Environmental Protection Agency Maximum Contaminant Level (MCL) of 0.185 Bq/L (5 pCi/L) for combined Ra (226Ra plus 228Ra) for drinking water was exceeded in 4.02% (39 of 971) of samples for which both 226Ra and 228Ra were determined, or in 3.15% (40 of 1266) of the samples in which at least one isotope concentration (226Ra or 228Ra) was determined. The maximum concentration of combined Ra was 0.755 Bq/L (20.4 pCi/L) in water from the North Atlantic Coastal Plain quartzose sand aquifer system. All the exceedences of the MCL for combined Ra occurred in water samples from the following 7 PAs (in order of decreasing relative frequency of occurrence): the Midcontinent and Ozark Plateau Cambro-Ordovician dolomites and sandstones, the North Atlantic Coastal Plain, the Floridan, the crystalline rocks (granitic, metamorphic) of New England, the Mesozoic basins of the Appalachian Piedmont, the Gulf Coastal Plain, and the glacial sands and gravels (highest concentrations in New England).  相似文献   

6.
In this study, radioactivity measurements in the environment of Akhisar, Gölmarmara, Gördes and Sindirgi regions in Western Turkey were investigated in order to evaluate the implications of any excess radioactivity in the environment of geological formation. The radioactivity concentrations of 40K, 238U and 232Th radionuclides in the soil samples were measured by a NaI(Tl) gamma spectrometer system, and the radium activity concentrations in the water samples were also analyzed by an ZnS(Ag) alpha counter by the collector chamber method. The radioactivity of 40K, 238U and 232Th in soils ranged 2.80–2,347.77, 9.90–256.19 and 9.66–106.53 Bq kg?1, respectively. The activity of 226Ra in the water samples ranged from 0.03 Bq L?1 (0.89pCi/L) to 0.80 Bq L?1 (21.58pCi/L). In addition, the external terrestrial gamma dose rate in air (nGy h?1), annual effective dose rate (mSv year?1) and radium equivalent activity (Bq kg?1) were calculated and compared with international standard values.  相似文献   

7.
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   

8.
The increasing interest in radioactivity has brought about the need for an assessment of human exposure to radiation. It is, therefore, necessary to examine naturally occurring radioactivity in the environment, especially its occurrence in groundwater. The aim of this work was then to study the levels and behavior of the most significant natural radionuclides, also in order to improve the knowledge of the hydrochemical processes involved in the selected groundwater systems. Natural radioactivity in fifteen Calabrian groundwaters for human use was investigated through high-resolution gamma spectrometry (with a negative-biased Ortec HPGe detector) and liquid scintillation measurements. Particular attention was given on those radionuclides (3H, 238U, 226Ra, and 228Ra), which contribute in a significant way to the overall effective dose received by members of the public due to the intake of drinking water originating from groundwater systems. The activity concentration of 238U varied from 1 to 51 mBq/L, as a result of the geology of the investigated area and of the oxidizing conditions that favored U dissolution. 226Ra presented a broad range of activity concentrations (0.011–0.14 mBq/L), lower than uranium ones because radium occurs in groundwater under reducing conditions. Some heavy metals (Cd, Pb, Be, Hg, Ag, As, Tl, Sb, Se, and Ni) were also investigated through ICP-MS measurements and compared with the limits set by the Italian Legislation. Metals are released into the environment by both natural and anthropogenic sources; they leach into underground waters, moving along water pathways and eventually depositing in the aquifer.  相似文献   

9.
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   

10.
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   

11.
The correlation between specific activities of some natural radionuclides (238U, 226Ra, 232Th, 40K) measured in sediment taken from river bottom was studied. The sediment was taken from the Serbian part of the Danube River. Good correlation between some of the isotopes is observed, so that their specific activity ratios are spread over a lower range than specific activities themselves. This suggests that evaluation of specific activity ratios of some natural radionuclides could be a more sensitive method for the determination of increased levels of some of them than the straightforward analysis of specific activities.  相似文献   

12.
Factors controlling the groundwater transport of U, Th, Ra, and Rn   总被引：1，自引：0，他引：1  
A model for the groundwater transport of naturally occurring U, Th, Ra, and Rn nuclides in the238U and232Th decay series is discussed. The model developed here takes into account transport by advection and the physico-chemical processes of weathering, decay, α-recoil, and sorption at the water-rock interface. It describes the evolution along a flowline of the activities of the238U and232Th decay series nuclides in groundwater. Simple sets of relationships governing the activities of the various species in solution are derived, and these can be used both to calculate effective retardation factors and to interpret groundwater data. For the activities of each nuclide, a general solution to the transport equation has been obtained, which shows that the activities reach a constant value after a distance ϰi, characteristic of each nuclide. Where ϰi is much longer than the aquifer length, (for238U,234U, and232Th), the activities grow linearly with distance. Where gKi is short compared to the aquifer length, (for234Th,230Th,228Th,228Ra, and224Ra), the activities rapidly reach a constant or quasi-constant activity value. For226Ra and222Rn, the limiting activity is reached after 1 km. High δ234U values (proportional to the ratioɛ234Th/W238U) can be obtained through high recoil fraction and/or low weathering rates. The activity ratios230Th/232Th,228Ra/226Ra and224Ra/226Ra have been considered in the cases where either weathering or recoil is the predominant process of input from the mineral grain. Typical values for weathering rates and recoil fractions for a sandy aquifer indicate that recoil is the dominant process for Th isotopic ratios in the water. Measured data for Ra isotope activity ratios indicate that recoil is the process generally controlling the Ra isotopic composition in water. Higher isotopic ratios can be explained by different desorption kinetics of Ra. However, the model does not provide an explanation for228Ra/226Ra and224Ra/226Ra activity ratios less than unity. From the model, the highest222Rn emanation equals 2ɛ. This is in agreement with the hypothesis that222Rn activity can be used as a first approximation for input by recoil (Krishnaswamiet al 1982). However, high222Rn emanation cannot be explained by production from the surface layer as formulated in the model. Other possibilities involve models including surface precipitation, where the surface layer is not in steady-state.  相似文献   

13.
This paper describes the use of 210Pb and 137Cs radioactivity measurements to determine the rates of sedimentation in the Great Lakes. Cores from eight locations in Lake Michigan were chosen for examination to cover as wide as possible a range of sedimentation rates and representative sedimentary environments. The surficial 210Pb activity in the sediments varies between 7 and 23 pCi/g dry wt and its profile in each core shows the expected exponential decrease with depth consistent with the assumption of uniform sedimentation rate over the last hundred years and secular equilibrium between supported 210Pb and 226Ra (0.5-1.0 pCi/g dry wt). Companion measurements of 137Cs indicate that the coring technique satisfactorily recovered the uppermost levels of the deposit and that the mobility of both radionuclides within the sediment is probably small.Based on the limited number of cores analyzed to date, it appears that modern sedimentation rates are not very different from average rates for the last 7000 yr. The excess 210Pb appears to originate primarily from atmospheric fallout, but a further inventory of the 210Pb distribution over the lake bottom must be made to properly assess the significance of other sources. The spatial distributions of both 137Cs and 210Pb at certain stations suggest that the mode of transport of these radionuclides are comparable and involve attachment to settling particles. A mathematical model is developed which accounts for the observed limited mobility of both 210Pb and 137Cs in several of the cores in terms of post-depositional redistribution by physical or biological mixing processes.  相似文献   

14.
Submarine groundwater discharge (SGD) is herein recognized as a significant pathway of material transport from land to the coastal SW Atlantic Ocean and thus, it can be a relevant factor affecting the marine biogeochemical cycles in the region. This paper focuses on the initial measurements of 226Ra, 228Ra and 222Rn made in Patagonia’s coastal zone of Chubut and Santa Cruz provinces (42°S–48°S, Argentina). 226Ra activity ranged from 2.9 to 73.5 dpm 100 L?1, and 228Ra activity ranged from 11.9 to 311.0 dpm 100 L?1 in groundwater wells. The radium activities found in Patagonia’s marine coastal regions and adjacent shelf indicate significant enrichment throughout the coastal waters. Groundwater samples presented the largest 222Rn activity and ranged from 2.66 to 1083 dpm L?1. Conversely, in the coastal marine environment, the 222Rn activity ranged from 1.03 to 6.23 dpm L?1. The Patagonian coastal aquifer showed a larger enrichment in 228Ra than in 226Ra, which is a typical feature for sites where SGD is dominant, probably playing a significant role in the biogeochemistry of these coastal waters.  相似文献   

15.
《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   

16.
The unadjusted 72-h gross alpha activities in water from two wells completed in marine and alluvial deposits in a coastal southern California aquifer 40 km north of San Diego were 15 and 25 picoCuries per liter (pCi/L). Although activities were below the Maximum Contaminant Level (MCL) of 15 pCi/L, when adjusted for uranium activity; there is concern that new wells in the area may exceed MCLs, or that future regulations may limit water use from the wells. Coupled well-bore flow and depth-dependent water-quality data collected from the wells in 2011 (with analyses for isotopes within the uranium, actinium, and thorium decay-chains) show gross alpha activity in marine deposits is associated with decay of naturally-occurring 238U and its daughter 234U. Radon activities in marine deposits were as high as 2230 pCi/L. In contrast, gross alpha activities in overlying alluvium within the Piedra de Lumbre watershed, eroded from the nearby San Onofre Hills, were associated with decay of 232Th, including its daughter 224Ra. Radon activities in alluvium from Piedra de Lumbre of 450 pCi/L were lower than in marine deposits. Chromium VI concentrations in marine deposits were less than the California MCL of 10 μg/L (effective July 1, 2014) but δ53Cr compositions were near zero and within reported ranges for anthropogenic chromium. Alluvial deposits from the nearby Las Flores watershed, which drains a larger area having diverse geology, has low alpha activities and chromium as a result of geologic and geochemical conditions and may be more promising for future water-supply development.  相似文献   

17.
《Applied Geochemistry》2001,16(1):109-122
The purpose of this study was to elucidate the processes controlling the distribution and behavior of the longer-lived Ra isotopes in continuous Paleozoic carbonate aquifers of parts of Missouri, Kansas, and Oklahoma. Activities of (228Ra) and (226Ra) were analyzed in fresh and saline ground waters, brines, and rocks. The fluids have a wide salinity range (200–250,000 mg l−1 total dissolved solids). The (226Ra) activity ranges from 0.66–7660 dpm kg−1 and correlates with salinity and other alkaline earth element (Ca, Sr, and Ba) concentrations. The range of (228Ra:226Ra) ratios in the fluids (0.06–1.48) is similar to that in the aquifer rocks (0.21–1.53). The relatively low mean fluid (228Ra:226Ra) ratio (0.30) reflects the low Th:U ratio of the predominant carbonate aquifer rock. Radium occurs mostly (≥77%) as Ra2+ species in the fluids. Salinity-dependent sorption–desorption processes (with log K values from 100–104 and negatively correlated with salinity), involving Th-enriched surface coatings on aquifer flow channels, can explain the rapid solid–fluid transfer of Ra isotopes in the system and the correlation of Ra with salinity.  相似文献   

18.
A study of natural radionuclides and radon concentration of Hamirpur District of Himachal Pradesh, India is carried out using various methodologies. The activity concentration of the natural radionuclides viz. 226Ra, 232Th and 40K is measured using high-resolution-based HPGe detector. Indoor radon measurements in the dwellings of Hamirpur district is carried out using LR-115 type II cellulose nitrate films in the bare mode. The average activity concentrations of 226Ra, 232Th and 40K are 35.58, 54.95 and 580.58 Bq kg?1, respectively. The annual average indoor radon value in the study area varies from 173.90 to 198.25 Bq m?3, which is well within the recommended action level given by International Commission on Radiological Protection. The indoor radon values obtained in the present investigation are higher than the world average of 40 Bq m?3. Radon concentration in water samples is measured using RAD7, an active radon detector. The annual effective dose for stomach and lung is determined from the measured value of radon concentration in water. To assess the radiation hazard of the natural radioactivity in all samples to the people, the radium equivalent activity, external hazard index, lifetime fatality risk, absorbed dose rate and total annual effective dose is estimated. The results signify that the studied area does not possess any radiation hazards due to the presence of natural radioactivity concentration.  相似文献   

19.
Naturally-occurring radionuclides (uranium, radium, and radon), major dissolved constituents, and trace elements were investigated in fresh groundwater in 117 wells in fractured crystalline rocks from the Piedmont region (North Carolina, USA). Chemical variations show a general transition between two water types: (1) slightly acidic (pH 5.0–6.0), oxic, low-total dissolved solids (TDS) waters, and (2) near neutral, oxic to anoxic, higher-TDS waters. The uranium, radium, and radon levels in groundwater associated with granite (Rolesville Granite) are systematically higher than other rock types (gneiss, metasedimentary, and metavolcanic rocks). Water chemistry plays a secondary role on radium and radon distributions as the 222Rn/226Ra activity ratio is correlated with redox-sensitive solutes such as dissolved oxygen and Mn concentrations, as well as overall dissolved solids content including major divalent cations and Ba. Since 224Ra/228Ra activity ratios in groundwater are close to 1, we suggest that mobilization of Ra and Rn is controlled by alpha recoil processes from parent nuclides on fracture surfaces, ruling out Ra sources from mineral dissolution or significant long-distance Ra transport. Alpha recoil is balanced by Ra adsorption that is influenced by redox conditions and/or ion concentrations, resulting in an approximately one order of magnitude decrease (~ 20,000 to ~ 2000) in the apparent Ra distribution coefficient between oxygen-saturated and anoxic conditions and also across the range of dissolved ion concentrations (up to ~ 7 mM). Thus, the U and Th content of rocks is the primary control on observed Ra and Rn activities in groundwater in fractured crystalline rocks, and in addition, linked dissolved solids concentrations and redox conditions impart a secondary control.  相似文献   

20.
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   

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