The natural radioactivity in Guarani aquifer groundwater, Brazil.

The measurements of gross alpha and gross beta radioactivity in groundwater samples from Guarani aquifer in Brazil are reported in this paper together with the activity concentration of the natural dissolved radionuclides (40)K, (238)U, (234)U, (226)Ra, (222)Rn, (210)Po, (210)Pb, (232)Th, (228Th), and (228)Ra. Most of the gross alpha radioactivity values were below the critical level of detection corresponding to 1mBq/L, however, the whole data set for the gross beta radioactivity and radionuclides (40)K, (238)U, (234)U, (226)Ra, (222)Rn, (210)Po, (210)Pb, and (228)Ra was submitted to a statistical treatment, considering class intervals arranged in geometric progression, because of the great variability of the activity. The analysis indicated lognormal distribution of the data, as usually observed in samples taken from the natural context. An inverse relationship between the gross alpha and gross beta activity has been identified and is related to an increase in the K content in the water. The mobility coefficient has been estimated for (238)U, (226)Ra, (232)Th and (228)Ra in Guarani aquifer and the results indicated that the radioelement solubility in the studied system varies according to the following order: radium>uranium>thorium. The implications of the data obtained in terms of standards established for defining the drinking water quality have also been discussed.     

Certified reference material for radionuclides in fish flesh sample IAEA-414 (mixed fish from the Irish Sea and North Sea).

A certified reference material (CRM) for radionuclides in fish sample IAEA-414 (mixed fish from the Irish Sea and North Seas) is described and the results of the certification process are presented. Nine radionuclides (40K, 137Cs, 232Th, 234U, 235U, 238U, 238Pu, 239+240Pu and 241Am) were certified for this material. Information on massic activities with 95% confidence intervals is given for six other radionuclides (90Sr, 210Pb(210Po), 226Ra, 239Pu, 240Pu 241Pu). Less frequently reported radionuclides (99Tc, 129I, 228Th, 230Th and 237Np) and information on some activity and mass ratios are also included. The CRM can be used for quality assurance/quality control of the analysis of radionuclides in fish sample, for the development and validation of analytical methods and for training purposes. The material is available from IAEA, Vienna, in 100 g units.     

Classification of soil samples according to geographic origin using gamma-ray spectrometry and pattern recognition methods.

Multivariate data analysis methods were used to recognize and classify soils of unknown geographic origin. A total of 103 soil samples were differentiated into classes, according to regions in Serbia and Montenegro from which they were collected. Their radionuclide (226Ra, 238U, 235U, 40K, 134Cs, 137Cs, 232Th and 7Be) activities detected by gamma-ray spectrometry were then used as the inputs in different pattern recognition methods. For the classification of soil samples using eight selected radionuclides, the prediction ability of linear discriminant analysis (LDA), k-nearest neighbours (kNN), soft independent modelling of class analogy (SIMCA) and artificial neural network (ANN) were 82.8%, 88.6%, 60.0% and 92.1%, respectively.     

Investigation of the soil-plant transfer of primordial radionuclides in tomatoes by low-level gamma-ray spectrometry.

The paper presents actual data from investigations of the soil-plant transfer of the primordial radionuclides 40K, 238U, 226Ra, 210Pb and 227Ac for tomatoes growing at soils from former uranium mining areas. The analysis were carried out using low-level gamma-ray spectrometry in a 47 m deep underground laboratory. For tomato fruits transfer factors of (0.0007 +/- 0.0006) for 235U, (0.0021 +/- 0.0017) for 226Ra, (0.0015 +/- 0.0009) for 210Pb and (0.0018 +/- 0.0012) for 227Ac were obtained. The investigation of the soil-plant transfer by low-level gamma-ray spectrometry is often limited by the Compton-continuum from the always present high-energy gamma-ray emitter 40K.     

Behavior and environmental impacts of radionuclides during the hydrometallurgy of calcareous and argillaceous rocks, southwestern Sinai, Egypt

The hydrometallurgy of radionuclides means getting the radioelements from the rocks into solution by leaching, getting the radionuclides from the solution by extraction process, and then precipitation of the desired elements to obtain concentrate. The follow-up of the radionuclides during these processes is the main target of this work to identify the identity of the original samples, pregnant solutions (leachates), residuals and the concentrate. Six samples were chosen to achieve this work. The leaching process was carried out under the conditions; 20-30% acid (H(2)SO(4)) concentration, 1:3 solid/liquid ratios, 60 min stirring time at room temperature. The activity concentrations of (238)U, (235)U, (234)U, (226)Ra, (214)Pb, (214)Bi, (232)Th and (40)K were measured in the original samples, residuals and U-concentrate (Bq/kg), and leachates (Bq/?). The results indicate that, the radionuclides before (226)Ra in the (238)U decay series are more leachable (released) than those from (226)Ra to (214)Bi in the order; (234)U>(238)U=(235)U > (226)Ra>(214)Pb>(214)Bi. (232)Th and (40)K are immobile under the present conditions. The radiological hazards of natural radioactivity in the original samples, leachates, residuals and U-concentrate were calculated and compared with the internationally recommended values and were found to be much higher than the world average values.     

Distribution of natural and anthropogenic radionuclides in soil and beach sand samples of Kalpakkam (India) using hyper pure germanium (HPGe) gamma ray spectrometry.

Pre-operational survey at Kalpakkam coast, indicated elevated gamma background radiation levels in the range of 100-4000 nGy h(-1) over the large tracts of the coastal sands due to the presence of pockets of monazite mineral in beach sands. In view of the prevalence of monazite, a systematic gamma spectrometric study of distribution of natural radionuclides in soil and beach sand samples collected from the terrestrial and coastal environment of Kalpakkam was performed and concentrations of primordial radionuclides such as 238U, 232Th and 40K and anthropogenic radionuclide 137Cs were determined. The concentrations of 238U, 232Th and 40K in soil samples were 5-71, 15-776 and 200-854 Bq kg(-1) dry, respectively. In beach sand samples, 238U, 232Th and 40K contents varied in the range of 36-258, 352-3872 and 324-405 Bq kg(-1) dry, respectively. The total absorbed gamma dose rate in air due to the presence of 238U, 232Th and 40K in Kalpakkam soil samples varied between 24 and 556 nGy h(-1) with a mean of 103 nGy h(-1). The contribution to the total absorbed gamma dose rate in air in the decreasing order was due to the presence of 232Th (76.4%), followed by 40K (16.9%) and 238U (6.7%) in Kalpakkam soils. However, in beach areas of Kalpakkam, the presence of 232Th in beach sand contributed maximum (94.0%) to the total absorbed gamma dose rate in air followed by 238U (4.7%) and minimum contribution was by 40K (1.3%). 137Cs in Kalpakkam soils ranged from < or = 1.0 to 2.8 Bq kg(-1) dry, which was 1-3 order of magnitude less than the concentration of primordial radionuclides in soil.     

Distribution of 226Ra, 232Th and 40K in soils and sugar cane crops at Corumbataí river basin,São Paulo State,Brazil

The common use of phosphate fertilizers NPK and amendments in sugar cane crops in Brazilian agriculture may increase the ²²⁶Ra, ²³²Th and ⁴⁰K activity concentrations in soils and their availability for plants and human food chain. Thus, the main aim of this study was to evaluate the distribution of ²²⁶Ra, ²³²Th and ⁴⁰K in soils and sugar cane crops in the Corumbataí river basin, São Paulo State, Brazil. The gamma spectrometry was utilized to measure the ²²⁶Ra, ²³²Th and ⁴⁰K activity concentration in all samples. The soil-to-sugar cane transfer factors (TF) were quantified using the ratio between the radionuclide activity concentration in sugar cane and its activity concentration in soil. The results show that, although radionuclides incorporated in phosphate fertilizers and amendments are annually added in the sugar cane crops, if utilized in accordance with the recommended rates, their use does not lead to hazards levels in soils. The soil-to-sugar cane transfer of radionuclides occurred in the following order ⁴⁰K>²²⁶Ra>²³²Th. Therefore, under these conditions, radionuclides intake through consumption of sugar is not hazardous to human health.     

Investigation of natural radioactivity levels in water around Kadugli, Sudan.

Surface water from Miri Lake and groundwater from around Kadugli (West-Central Sudan) obtained by means of hand-pumps was analysed for (238)U, (226)Ra, (222)Rn, and (232)Th activity concentrations. The surface water showed very low levels of radionuclide concentrations: <1.0-7.5, 8.5-16.5, <1.6, and <0.1-0.39mBqL(-1) for (238)U, (226)Ra, (222)Rn, and (232)Th, respectively. Groundwater revealed a significant amount of natural radioactivity (16.1-1720, 7.7-14.3, 3000-139,000, <0.1-39mBqL(-1)) respectively. The overall annual effective dose was below the WHO reference dose level of 0.1mSvyr(-1) except in one groundwater sample with an associated dose of 0.7mSvyr(-1).     

The effect of uranium migration on radionuclide distributions for soil samples at the El-Gor area,Sinai, Egypt

The concentrations and distributions of the activity of natural radionuclides in soil samples were investigated in fifteen soil samples at El-Gor area representing two profiles (A and B) using a HP–Ge detector and alpha counting by SSNTD (CR-39), respectively. The average concentrations of the radionuclides ²³⁸U, ²²⁶Ra, ²³⁵U, ²³²Th and ⁴⁰K are 203.4, 177.23, 9.77, 43.33 and 386.22 Bq kg⁻¹ (dry weight), respectively, and profile A and ²³⁸U, ²²⁶Ra, ²³⁵U, ²³²Th and ⁴⁰K have average concentrations of 232.58, 246, 11.7, 31.7, and 277.07 Bq kg⁻¹ for profile B, respectively. The eTh and eU were estimated to detect the migration process of uranium into or out of an area or uranium to or from the studied profiles. The results indicate a migration of uranium by 29% for profile A and 65.37% for profile B. The activity ratio (²³⁸U/²²⁶Ra) was found to be 0.9 in profile A and 1.15 in profile B. These ratios coincide with the uranium migration processes. The responsible mass corresponding to the measured ²²⁶Ra activity was also calculated. The radon activity concentrations for the two profiles are nearly 300 Bq m⁻³. The emanation coefficient (η) was calculated from the ratio of the expected radon activity to the measured radon for the studied soil samples. The value of η was found to depend only on the radium activity regardless to soil formation.     

云南省部分地区环境放射性水平调查及居民所受外照射剂量估算

目的 探讨云南省部分地区的环境放射性水平及所致居民外照射剂量。方法 通过对表层土壤、近地面空气气溶胶和水中放射性核素的γ能谱测量分析,利用卫生系统全国土壤调查中选用的模式,估算环境中²³⁸U、²²⁶Ra、²³²Th、⁴⁰K和¹³⁷Cs所致居民的受照剂量。利用美国航空管理局的CARI-6软件,估算了调查地区居民的宇宙辐射剂量。 结果 调查地区近地面空气气溶胶和水样中各核素比活度都低于探测下限。土壤中放射性核素所致居民人均外照射年有效剂量为0.5206 mSv/年,其中,0.52 mSv/年来自土壤中天然放射性核素,0.6 μSv/年来自土壤中¹³⁷Cs。宇宙辐射所致居民剂量为0.61 mSv/年。结论 宇宙辐射和土壤中天然辐射对居民所受外照射剂量贡献为99.95%,人工放射性核素¹³⁷Cs所致居民的外照射剂量贡献仅为0.05%。     

Radioactivity levels of recent sediments in the Butrint Lagoon and the adjacent coast of Albania.

Sediment samples have been collected in the Butrint area, located in the south-west Albania to determine the radioactivity levels of (40)K, (137)Cs, (212)Bi, (212)Pb, (214)Bi, (214)Pb, (226)Ra and (228)Ac on the bed of the lagoon and adjacent sea, using direct counting gamma spectroscopy. The concentration of (137)Cs and (40)K varied from 2.8 to 37.5 Bq/kg and from 266 to 675 Bq/kg dry weight (dw), respectively (central values). The average concentrations of (238)U and (232)Th daughter products varied from 8 to 27 Bq/kg and from 13 to 40 Bq/kg dw, respectively. The measured (235)U activity ranged from 0.7 to 2.5 Bq/kg dw. Samples of different sedimentary properties, studied for the radioactivity concentration, revealed an inversely proportional relation between grain size and a linear combination of measured specific activities of (226)Ra, (232)Th ((228)Ac, (212)Bi and (212)Pb), (40)K and (137)Cs.     

Study of natural radioactivity and the state of radioactive disequilibrium in U-series for rock samples, North Eastern Desert, Egypt.

Twenty rock samples collected from North Eastern Desert in Egypt have been investigated. Natural radionuclide contents have been measured by gamma-ray spectrometry employing a shielded HPGe detector. The activities of (238)U, (232)Th and (40)K have been determined in Bq/kg dry weight. The absorbed dose rate of gamma radiation ranged from 100.48 to 22,140.53 nGy/h. The representative external hazard index values (H(ex)) for the corresponding samples were estimated. In the present work, the state of radioactive disequilibrium in the U-series at Wadi Baligh area was studied. The activity ratios between (226)Ra/(214)Pb and (214)Pb/(214)Bi were measured. The thorium-to-uranium concentration ratios (Clark value) were also estimated.     

Transfer of 238U, 230Th, 226Ra,and 210Pb from soils to tree and shrub species in a Mediterranean area

The soil-to-plant transfer factors of natural uranium isotopes (²³⁸U and ²³⁴U), ²³⁰Th, ²²⁶Ra, and ²¹⁰Pb were studied in a disused uranium mine located in the Extremadura region in the south-west of Spain. The plant samples included trees (Quercus ilex, Quercus suber, and Eucalyptus cameldulensis) and one shrub (Cytisus multiflorus). All of them are characteristic of Mediterranean environments. The activity concentrations in leaves and fruit were determined for the tree species at different stages of growth. For the shrub, the total above-ground fraction was considered in three seasons. For old leaves and fruit, the highest activity concentrations were found in Eucalyptus cameldulensis for all the radionuclides studied, except in the case of ²³⁰Th that presented similar activity concentrations in all of the tree species studied. In every case, the transfer to fruit was less than the transfer to leaves. In the shrub, the results depended on the season of sampling, with the highest value obtained in spring and the lowest in autumn. Important correlations were obtained for ²³⁸U and ²²⁶Ra between the activity ratio in soils with that in leaves or fruit.     

Natural radioactivity in Algerian building materials.

Samples of natural and manufactured building materials collected from Algiers have been analysed for 226Ra, 232Th and 40K using a high-resolution HPGe gamma-spectrometry system. The specific concentrations for 226Ra, 232Th and 40K, from the selected building materials, ranged from (12-65 Bq kg(-1)), (7-51 B qkg(-1)) and (36-675 Bq kg(-1)), respectively. The measured activity concentrations for these natural radionuclides were compared with the reported data of other countries and with the world average activity of soil. Radium-equivalent activities were calculated for the measured samples to assess the radiation hazards arising from using those materials in the construction of dwellings. All building materials showed Ra(eq) activities lower than the limit set in the OECD report (370 Bq kg(-1)), equivalent to external gamma-dose of 1.5 mSv yr(-1).     

Prediction of peak-to-background ratio in gamma-ray spectrometry using simplex optimized artificial neural network.

An artificial neural network (ANN) model was used for the prediction of peak-to-background ratio (PBR) as a function of measurement time in gamma-ray spectrometry. In order to make the ANN model with good predictive power, the ANN parameters were optimized simultaneously employing a variable-size simplex method. Most of the predicted and the experimental PBR values for eight radionuclides ((226)Ra, (238)U, (235)U, (40)K, (232)Th, (134)Cs, (137)Cs, and (7)Be) commonly detected in soil samples agreed to within +/-19.4% of the expanded uncertainty and 2.61% of average bias.     

Disequilibrium in naturally occurring radioactive series in some phosphate ores

Eight phosphate ore samples from Egypt and Saudi Arabia were studied by atomic absorption spectrometry for the Bi, Pb, Th and Al concentrations in ppm or ppb or per cent. Also X-ray diffraction spectrometry was applied for determining the mineral and chemical composition of the phosphate ore samples. A gamma spectrometry system, based on HPGe crystal, was applied for determining the concentrations of the radioactive elements in (238)U, (226)Ra and (232)Th series as well as (40)K, in Bq/kg dry weight. Concentrations in ppm were found to be from <10.0 to 20.48, from <7.50 to 27.30 and from <1.0 to 50.0 for Bi, Pb and Th, respectively. Al ranged from <0.05 to 3.13%. Major, minor and trace chemical and mineral compositions were assigned for each sample by XRD spectrometry. Concentrations of the different elements in both radioactive series, (238)U, (226)Ra and (232)Th were compared. Disequilibrium was found in both series.     

Impact of phosphate industry on the environment: a case study.

This paper presents results obtained from studying the impact of the Syrian phosphate industry on the environment. This work is based on evaluating naturally occurring radionuclide concentrations in the surrounding environment at the locations of this industry, viz. mines, phosphate fertilizers factory and phosphate export platforms. Air particulates, soil, water (river, lake and sea water), biota and plant samples were collected and analyzed. Natural radionuclides ((226)Ra, (nat)U, (210)Po, (210)Pb) were determined by means of low background gamma spectrometry and alpha spectrometry. The results showed that the distribution and enhancement of natural radionuclides in the surrounding environment in these three locations are mainly due to fallout of phosphate dust generated during loading and processing of phosphate ore. The extent of contamination was related to climate conditions. Radon gas and its daughters generated from phosphate ores were found to be the main source of enhanced concentrations of (210)Po and (210)Pb in soil and leafy plants. These results can be considered as baseline data and can be used to prove the effectiveness of any future pollution controls adopted.     

Determination of the natural radioactivity levels in north west of Dukhan, Qatar using high-resolution gamma-ray spectrometry

This study is aimed at the determination of the activity concentrations of naturally occuring and technologically enhanced levels of radiation in 34 representative soil samples that have been collected from an inshore oil field area which was found to have, in a previous study, the highest observed value of 226Ra concentration among 129 soil samples. The activity concentrations of 238U and 226Ra have been inferred from gamma-ray transitions associated with their decay progenies and measured using a hyper-pure germanium detector. Details of the sample preparation and the gamma-ray spectroscopic analysis techniques are presented, together with the values of the activity concentrations associated with the naturally occuring radionuclide chains for all the samples collected from NW Dukhan. Discrete-line, gamma-ray energy transitions from spectral lines ranging in energy from ～100 keV up to 2.6 MeV have been associated with characteristic decays of the various decay products within the 235.8U and 232Th radioactive decay chains. These data have been analyzed, under the assumption of secular equilibrium for the U and Th decay chains. Details of the sample preparation and the gamma-ray spectroscopic analysis techniques are presented. The weighted mean value of the activity concentrations of 226Ra in one of the samples was found to be around a factor of 2 higher than the values obtained in the previous study and approximately a factor of 10 higher than the accepted worldwide average value of 35 Bq/kg. The weighted mean values of the activity concentrations of 232Th and 40K were also deduced and found to be within the worldwide average values of 30 and 400 Bq/kg, respectively. Our previous study reported a value of 201.9±1.5Stat.±13Syst.Bq/kg for 226Ra in one sample and further investigation in the current work determined a measured value for 226Ra of 342.00±1.9Stat.±25Syst.Bq/kg in a sample taken from the same locality. This is significantly higher than all the other investigated soil samples in the current and previous works. Notably, the Th levels in the same sample are within the worldwide average expectations, implying that the increased 226Ra concentration arises from TENORM processes.     

Determination of radioactivity levels and hazards of soil and sediment samples in Firtina Valley (Rize, Turkey).

The natural radioactivity levels in soil and sediment samples of Firtina Valley have been determined. To our knowledge, there seems to be no information about radioactivity level in the Firtina Valley soils and sediments so far. For this reason, soil and sediment samples were collected along the Firtina Valley and analysis on the collected samples were carried out to determine 238U, 232Th, 40K and 137Cs radioisotopes using high purity germanium detector. The activity concentrations obtained for 226Ra, 214Pb, 214Bi, 228Ac, 208Tl, 40K and 137Cs are given in the unit of Bq/kg. The results have been compared with other radioactivity measurements in different country's soils and sediments. The radium equivalent activity (Raeq), the absorbed dose rate (D), the external hazard index (Hex), the annual gonadal dose equivalent (AGDE) and the annual effective dose equivalent (AEDE) were also calculated and compared with the international recommended values.     

Factor analysis applied to distribution of elements in western Turkey.

This paper examines the results of R-mode factor analysis performed on four radionuclides and two elements data from a geochemical survey from western Turkey. Sediment and soil samples numbering 321 were collected along the Gediz river and analysed for 238eU, 232eTh, 40K, 226Ra, Mg and Pb. Two factors in soil and sediment, which account for 59% and 56% of the total variance, respectively, were extracted and named as geological structure and volcano.