Radioactive and stable metal bioaccumulation, crystalline compound and siderophore detection in Clavariadelphus truncatus

137Cs and 40K activity concentrations and stable elements have been measured in Clavariadelphus truncatus collected in Mexico. Iron-chelating compounds of siderophore-type was also studied in the species. 137Cs and 40K were determined in soil and mushroom samples with HpGe gamma-ray spectrometry. Macro- and micro-elemental concentrations were determined by XRF and ICP-MS. Siderophore detection was obtained with a colorimetric assay and X-ray diffraction analysis was performed using a Siemens D5000 diffractometer. 137Cs geometric mean concentration in C. truncatus was 26 times higher as compared with other Mexican edible mushroom species, while 40K showed stability. Soil-C. truncatus concentration ratio for 137Cs and other micro-elements such as Cs, Rb and Pb were also higher than other Mexican edible species. The 137Cs committed effective dose due to the ingestion of C. truncatus was 8 x 10(-6) Sv year(-1). The main crystalline structure found in C. truncatus was D-Mannitol.     

Radioactivity in trinitite six decades later

The first nuclear explosion test, named the Trinity test, was conducted on July 16, 1945 near Alamogordo, New Mexico. In the tremendous heat of the explosion, the radioactive debris fused with the local soil into a glassy material named Trinitite. Selected Trinitite samples from ground zero (GZ) of the test site were investigated in detail for radioactivity. The techniques used included alpha spectrometry, high-efficiency gamma-ray spectrometry, and low-background beta counting, following the radiochemistry for selected radionuclides. Specific activities were determined for fission products (90Sr, 137Cs), activation products (60Co, 133Ba, 152Eu, 154Eu, 238Pu, 241Pu), and the remnants of the nuclear fuel (239Pu, 240Pu). Additionally, specific activities of three natural radionuclides (40K, 232Th, 238U) and their progeny were measured. The determined specific activities of radionuclides and their relationships are interpreted in the context of the fission process, chemical behavior of the elements, as well as the nuclear explosion phenomenology.     

Distribution of gamma-ray emitting radionuclides in the environment of Burullus Lake: I. Soils and vegetations

The concentrations and distribution of gamma-ray emitting isotopes in Burullus Lake were investigated with the aim of evaluating the environmental radioactivity. Particularly in wetlands, natural properties of the environment can cause the actual inventory to be different from the activity originally deposited. The mean concentrations of (226)Ra, (232)Th and (40)K were 14.3, 15.5 and 224 Bq/kg, respectively, in the coastal soils. On the other hand, soil samples from the islands had mean concentrations of 13.5, 17.4 and 341 Bq/kg for (226)Ra, (232)Th and (40)K, respectively. Samples from coast and islands show evidence of possible transfer and accumulation of the (137)Cs radionuclide. The mean (137)Cs activity concentrations in the soil samples were 1.2 and 15.1 Bq/kg in the coast and islands, respectively. The vertical migration of (137)Cs was studied based on its content in the consequently located three soil layers down to 30 cm depth. The radium equivalent, dose rate in air and annual dose equivalent from the terrestrial natural gamma-radiation were evaluated. The mean activity concentrations of the gamma-ray emitting radionuclides in vegetation were relatively low.     

Survey of natural and anthropogenic radioactivity in environmental samples from Yugoslavia

The radioactivity of 238U, 226Ra, 232Th, 40K and 137Cs in sediments, soil, turf and honey from Serbia and Kosovo (Yugoslavia) was measured using gamma and alpha spectrometry in order to estimate the radiation hazard from natural and man-made sources, as well as to compile a database for radioactivity levels in those regions. One sample, collected in the vicinity of a "depleted uranium" (DU) shell of the recent Balkan war, revealed a high 238U activity and a non-natural 235U/238U activity ratio, confirming therefore its anthropogenic origin. However, some other soil samples coming from characteristic DU craters did not show any characteristic level of radioactivity. The other sediment and turf samples taken all around the country show low radioactivity levels for all the isotopes here considered. With the aim of obtaining some indication about radioactivity migration in the food chain, several honey samples have been examined too. All samples show very low radioactivity content, often indistinguishable from natural background.     

Determination of thorium, uranium and potassium elemental concentrations in surface soils in Cyprus

A comprehensive study was conducted to determine thorium, uranium and potassium elemental concentrations in surface soils throughout the accessible area of Cyprus using high-resolution gamma-ray spectrometry. A total of 115 soil samples was collected from all over the bedrock surface of the island based on the different lithological units of the study area. The soil samples were air-dried, sieved through a fine mesh, sealed in 1000-ml plastic Marinelli beakers, and measured in the laboratory in terms of their gamma radioactivity for a counting time of 18 h each. From the measured gamma-ray spectra, elemental concentrations were determined for thorium (range from 2.5 x 10(-3) to 9.8 microg g(-1)), uranium (from 8.1 x 10(-4) to 3.2 microg g(-1)) and potassium (from 1.3 x 10(-4) to 1.9%). The arithmetic mean values (A.M. +/- S.D.) calculated from all samples are: (1.2+/-1.7 microg g(-1)), (0.6+/-0.7) microg g(-1), and (0.4+/-0.3%), for thorium, uranium and potassium, respectively, which are by a factor of three-six lower than the world average values of 7.4 microg g(-1) (Th), 2.8 microg g(-1) (U) and 1.3% (K) derived from all data available worldwide. The best-fitting relation between the concentrations of Th and K versus U and also of K versus Th, is essentially of linear type with a correlation coefficient of 0.93, 0.84 and 0.90, respectively. The Th/U, K/U and K/Th ratios (slopes) extracted are equal to 2.0, 2.8 x 10(3) and 1.4 x 10(3), respectively.     

Fate of 60Co at a sludge land application site

Vertical distributions of (60)Co are determined in soil cores obtained from a 10-ha grassland, where anaerobically digested sludge was applied by surface spraying from 1986 to 1995 on the U.S. Department of Energy's Oak Ridge Reservation. These results, along with historical application records, are used to estimate vertical-migration rates and perform a mass balance. The presence of (60)Co results solely from the sludge-application process. Soil, vegetation, and surface-water samples were collected. Eleven soil cores were sectioned into 3-cm increments and analyzed by gamma-ray spectrometry. No (60)Co was detected in the vegetation or water samples. The downward migration rate of (60)Co in the upper 15cm of soil ranged from 0.50 to 0.73cm/yr. About 98%, 0.020+/-0.011Bq/cm(2), of (60)Co remained in the upper 15cm of soil, which compared favorably with the expected (60)Co activity based on historical records of 0.019+/-0.010Bq/cm(2).     

Natural radioactivity, dose assessment and uranium uptake by agricultural crops at Khan Al-Zabeeb, Jordan

Khan Al-Zabeeb, an irrigated cultivated area lies above a superficial uranium deposits, is regularly used to produce vegetables and fruits consumed by the public. Both soil and plant samples collected from the study area were investigated for their natural radioactivity to determine the uranium uptake by crops and hence to estimate the effective dose equivalent to human consumption. Concentrations of (238)U, (235)U, (232)Th, (226)Ra, (222)Rn, (137)Cs and (40)K in nine soil profiles were measured by gamma-ray spectrometry whereas watermelon and zucchini crops were analyzed for their uranium content by means of alpha spectrometry after radiochemical separation. Correlations between measured radionuclides were made and their activity ratios were determined to evaluate their geochemical behavior in the soil profiles. Calculated soil-plant transfer factors indicate that the green parts (leaves, stems and roots) of the studied crops tend to accumulate uranium about two orders of magnitude higher than the fruits. The maximum dose from ingestion of 1 kg of watermelon pulp was estimated to be 3.1 and 4.7 nSv y(-1) for (238)U and (234)U, respectively. Estimations of the annual effective dose equivalent due to external exposure showed extremely low values. Radium equivalent activity and external hazard index were seen to exceed the permissible limits of 370 Bq kg(-1) and 1, respectively.     

Multi-technique characterization of a nuclear bomb particle from the Palomares accident

A January 1966 accident dispersed Pu and other nuclear bomb materials in the vicinity of Palomares, a village in southeastern Spain. Radioactive particles were identified in a soil sample collected in 1998 and analytical results obtained from one of the isolated particles are presented here. Isolation of the particle was performed using gamma-ray spectrometry and imaging plates. Scanning electron microscopy with X-ray microanalysis revealed the presence of U and Pu as well as Pb and Fe in the particle of approximately 10microm diameter. Radioisotopes of U, Pu, and Am were quantified using radiometric methods, inductively coupled plasma mass spectrometry and secondary ion mass spectrometry. The elevated (235)U/(238)U atom ratio indicates enriched U, and the Pu atom ratios are consistent with weapons-grade material. This work demonstrates that the analysis of individual particles provides information not available through bulk sample analysis.     

Evaluation of Monte Carlo-based calibrations of HPGe detectors for in situ gamma-ray spectrometry

The aim of this work was to evaluate the use of Monte Carlo-based calibrations for in situ gamma-ray spectrometry. We have performed in situ measurements at five different sites in Sweden using HPGe detectors to determine ground deposition activity levels of ¹³⁷Cs from the 1986 Chernobyl accident. Monte Carlo-calculated efficiency calibration factors were compared with corresponding values calculated using a more traditional semi-empirical method. In addition, results for the activity ground deposition were also compared with activity densities found in soil samples. In order to facilitate meaningful comparisons between the different types of results, the combined standard uncertainty of in situ measurements was assessed for both calibration methods. Good agreement, both between the two calibration methods, and between in situ measurements and soil samples, was found at all five sites. Uncertainties in in situ measurements for the given measurement conditions, about 20 years after the fallout occurred, were found to be in the range 15–20% (with a coverage factor k = 1, i.e. with a confidence interval of about 68%).     

The extremely high 137Cs inventory in the Sulu Sea: a possible mechanism

Large-volume seawater samples were collected in the Sulu and South China Seas and their (137)Cs activities were determined by gamma-ray spectrometry using a low background type high-purity Ge detector. Vertical distributions of (137)Cs activity showed an exponential decrease in the South China Sea, whereas a subsurface maximum at 200m depth and monotonic decrease below 300m were observed in the Sulu Sea. A significant difference in intermediate water (137)Cs activities in the 500-2000m depth was observed between the Sulu and South China Seas, i.e., the (137)Cs activities in the Sulu Sea were remarkably higher than those in the South China Sea. The difference in the (137)Cs inventory below 500m was approximately 1200Bqm(-2) between the Sulu and South China Seas. The (137)Cs total inventory of 3200Bqm(-2) in the Sulu Sea was 5.7 times higher than that expected from global fallout. A possible mechanism controlling this extremely high (137)Cs total inventory may be inflows of the (137)Cs rich water masses through the Luzon Strait, lateral transport across the Mindoro Strait into the Sulu Sea, and then subduction into the deep layer in the basin.     

Seabed gamma-ray spectrometry: applications at IAEA-MEL

The technique of underwater gamma-ray spectrometry has been developed to complement or replace the traditional sampling-sample analysis approach for applications with space-time constraints, e.g. large areas of investigation, emergency response or long-term monitoring. IAEA-MEL has used both high-efficiency NaI(Tl) and high-resolution HPGe spectrometry to investigate contamination with anthropogenic radionuclides in a variety of marine environments. Surveys at the South Pacific nuclear test sites of Mururoa and Fangataufa have been used to guide sampling in areas of high contamination around ground zero points. In the Irish Sea offshore from the Sellafield nuclear reprocessing plant, a gamma-ray survey of seabed sediment was carried out to obtain estimates of the distribution and subsequently, for the inventory of 137Cs in the investigated area.     

Natural radioactivity measurements in the city of Ptolemais (Northern Greece)

Specific activities of the natural radionuclides (238)U, (226)Ra, (232)Th and (40)K were measured by means of gamma-ray spectrometry in surface soil samples collected from the city of Ptolemais, which is located near lignite-fired power plants. The mean activity values for (238)U, (226)Ra, (232)Th and (40)K were found to be 42+/-11, 27+/-6, 36+/-5 and 496+/-56 Bq kg(-1), respectively. These values fall within the range of typical world and Greek values for soil. The indoor radon concentration levels, which were also measured in 66 dwellings by means of SSNTD, ranged from 12 to 129 Bq m(-3), with an average value of 36+/-2 Bq m(-3). This value is close to world and Greek average values for indoor radon concentrations. The total effective dose due to outdoor external irradiation of terrestrial origin and to indoor internal irradiation from the short-lived decay products of (222)Rn was estimated to be 1.2 mSv y(-1) for adults, which is lower than the global effective dose due to natural sources of 2.4 mSv y(-1).     

Equilibrium of radiocesium with stable cesium within the biological cycle of contaminated forest ecosystems

Concentrations of (137)Cs and stable Cs were determined in plant, mushroom, lichen and soil samples collected at two forest sites with different contamination levels in Belarus in 1998. The concentration of (137)Cs in soil was the highest in near-surface organic layers (Of and Oh horizons) and decreased with depth in the mineral layers, whereas the concentrations of stable Cs were almost constant in the soil profile. The levels of (137)Cs and stable Cs in biological samples varied depending both on the species and the plant part sampled. Even though different species and parts of the same species were included, the concentration ratios of (137)Cs to stable Cs were fairly constant for samples collected at the same forest site, and were in the same order of magnitude as the (137)Cs to stable Cs ratios for the organic soil layers. This finding suggests that (137)Cs, mainly deposited on the forest ecosystems from the Chernobyl accident in 1986, was well mixed with stable Cs within the biological cycle in the forest ecosystems by 1998. The transfer factor for each biological sample of (137)Cs was almost the same as that of stable Cs, if they were calculated based on the concentrations in the Of + Oh layer. This suggests that the stable-Cs-based transfer factor could be used as equilibrium transfer factor of (137)Cs for different types of biological samples in the forest.     

Radioactivity concentrations of 40K, 134Cs, 137Cs, 90Sr, 241Am, 238Pu and 239+240Pu radionuclides in Jordanian soil samples

In November 2000, surface and core soil samples were collected from different regions of Jordan. The samples were analyzed by direct gamma spectrometry and combined radiochemical separation procedure to quantify (40)K, (134)Cs, (137)Cs, (90)Sr, (241)Am, (238)Pu and (239+240)Pu radioactivity. Concentrations (Bq.kg(-1) dry weight) have been observed to vary in the range 1.5-2.6 for (134)Cs, 2.8-11.4 for (90)Sr, and 0.13-0.48 for (241)Am, 0.016-0.062 for (238)Pu, 0.28-1.01 for (239+240)Pu and 155-543 for (40)K. The typical concentration of (137)Cs found in topsoils (0-2 cm) ranged in 7.5-576 Bq.kg(-1), dry weight. These values were greater than those observed in samples taken at greater depths (up to 32 cm). Activity ratios of (134)Cs/(137)Cs, (90)Sr/(137)Cs, (239+240)Pu/(137)Cs, (238)Pu/(137)Cs, (241)Am/(137)Cs, (239+240)Pu/(238)Pu and (241)Am /(238)Pu have mean values of 0.0049 (R=1), 0.29 (R=0.76), 0.41 (R=0.90), 0.39 (R=0.85), 0.41 (R=0.88), 7.72 (R=0.97) and 16.66 (R=0.98), respectively. The underlying concentrations were correlated and relatively higher than those reported in neighboring countries. One moss sample, as a biomonitor indicator, was measured and evaluated along with the soil samples. Its data showed higher concentrations of all measured radionuclides due to accumulations over years. The depth distribution of the fission product (137)Cs and the total deposition (Bq.m(-2)) were also studied in selected samples. Estimations of the annual effective dose equivalent due to (137)Cs-soil contamination showed values up to more than 200 microSv.     

Measurements of radiation level in petroleum products and wastes in Riyadh City Refinery

Recent concern has been devoted to the hazard arising from naturally occurring radioactive materials (NORM) in oil and gas facilities. Twenty-seven petroleum samples were collected from Riyadh Refinery. Fourteen samples were products and 13 were waste samples; three of them were scale samples and 10 were sludge samples. The specific radioactivities of (238)U, (232)Th, (226)Ra, (224)Ra, (40)K, and (235)U for all samples were determined using high-resolution gamma-ray spectrometry. The radium equivalent activity, radiation hazard indices and absorbed dose rate in air for all waste samples were estimated. The radon emanation coefficient of the waste samples was estimated. It ranged between 0.574 and 0.154. The age of two scale samples was determined and found to be 2.39 and 3.66 years. The chemical structure of the waste samples was investigated using X-ray florescence analysis (XRF) and Mg, Al, Si, S, Cl, Ca and Fe were found in all samples. From this study, it was noticed that the concentrations of the natural radionuclides in the petroleum wastes were higher than that of the petroleum products.     

Gamma-ray activity in the volcanic islands of the Southern Tyrrhenian Sea

Field gamma-ray spectrometry was used for the quantitative assessment of U, Th and K of rocks of Stromboli, Salina, Filicuidi and Panarea (Aeolian arc of the Southern Tyrrhenian, Italy). The air absorbed dose rate was calculated from radioelement concentrations. For some rocks the gamma-ray spectra were analysed with the three photo-peak methods and the response matrix method, which converts the pulse height distribution into the true incident gamma-ray energy spectrum. The higher values of U (8.2-9.8 ppm) coincide with higher Th (20.6-27.8 ppm) concentrations associated with rocks of shoshonitic composition. The spatial variation in radioelement concentration reflects the geochemical differences among the rocks. The air absorbed dose rate varies from 25 to 215 nGy h(-1). The highest values correspond to outcrops located in the eastern part of Stromboli, where the annual effective dose equivalent reaches a value of 264 microSv.     

Determination of extremely low (236)U/(238)U isotope ratios in environmental samples by sector-field inductively coupled plasma mass spectrometry using high-efficiency sample introduction

A method by inductively coupled plasma mass spectrometry (ICP-MS) was developed which allows the measurement of (236)U at concentration ranges down to 3 x 10(-14)g g(-1) and extremely low (236)U/(238)U isotope ratios in soil samples of 10(-7). By using the high-efficiency solution introduction system APEX in connection with a sector-field ICP-MS a sensitivity of more than 5,000 counts fg(-1) uranium was achieved. The use of an aerosol desolvating unit reduced the formation rate of uranium hydride ions UH(+)/U(+) down to a level of 10(-6). An abundance sensitivity of 3 x 10(-7) was observed for (236)U/(238)U isotope ratio measurements at mass resolution 4000. The detection limit for (236)U and the lowest detectable (236)U/(238)U isotope ratio were improved by more than two orders of magnitude compared with corresponding values by alpha spectrometry. Determination of uranium in soil samples collected in the vicinity of Chernobyl nuclear power plant (NPP) resulted in that the (236)U/(238)U isotope ratio is a much more sensitive and accurate marker for environmental contamination by spent uranium in comparison to the (235)U/(238)U isotope ratio. The ICP-MS technique allowed for the first time detection of irradiated uranium in soil samples even at distances more than 200 km to the north of Chernobyl NPP (Mogilev region). The concentration of (236)U in the upper 0-10 cm soil layers varied from 2 x 10(-9)g g(-1) within radioactive spots close to the Chernobyl NPP to 3 x 10(-13)g g(-1) on a sampling site located by >200 km from Chernobyl.     

Monte Carlo calculation of entire in situ gamma-ray spectra

We present a method for the synthesis of entire in situ gamma-ray spectra based on Monte Carlo calculations and measured data that characterize the detector properties. The method can serve for the determination of the effective depth of 137Cs in soil based on the information contained in the low-energy part of an in situ spectrum. Effective depth is defined as the depth of a plane distribution of 137Cs beneath the surface that reproduces the fluence energy and angular distribution at 1 m above the ground of gamma rays belonging to the real 137Cs distributions. We managed to reproduce the measured in situ spectra with our method and to demonstrate that the method allows the determination of the effective depth of 137Cs with a precision of 10(-2) m. The method requires minimal experimental characterization of the detector and is not sensitive to the details of the detector model and the soil composition and density employed in the Monte Carlo calculations.     

Radiocesium contamination behavior and its effect on potassium absorption in tropical or subtropical plants

The accumulation and long-term decline of radiocesium contamination in tropical plant species was studied through measurements of gamma-ray spectra from pomegranate (Punica granatum) and chili pepper (Capsicum fructescens) trees. The plants were originally grown at a (137)Cs contaminated site (where a radiological accident occurred in the city of Goiania, Brazil, in 1987), and transplanted to uncontaminated soil, so that the main source of contamination of the new leaves and fruits would be the fraction of the available radiocesium in the body of the plants. Measurements of (137)Cs and (40)K concentrations along the roots, main trunk, twigs, leaves and fruits before and after the transplant process of both plant species indicated a direct competition between Cs and K ions, suggesting that these elements could have a common accumulation mechanism. Cesium transfer factors from soil to pomegranate, green and red chili pepper fruits were evaluated as 0.4 +/- 0.1, 0.06 +/- 0.01 and 0.05 +/- 0.01, respectively. Biological half-life values due to (137)Cs translocation from the tree reservoir (BHL(T)) were calculated as 0.30 years for pomegranate, 0.12 years and 0.07 years for red and green peppers, respectively.     

The investigation of 137Cs and 90Sr background radiation levels in soil and plant around Tianwan NPP, China

(137)Cs and (90)Sr background levels in soil and plant around Tianwan Nuclear Power Plant (NPP) are reported. Eighty-four soil samples and 44 plant samples were collected from March 2000 to April 2002. The samples were analyzed by gamma spectrometry and radiochemical separation procedure to quantify (137)Cs and (90)Sr radioactivities. The concentrations (Bqkg(-1) dry weight) have been observed in the range of 0.6-1.6 for (90)Sr and 1.4-6.9 for (137)Cs in soils, their average values are 1.0+/-0.3 and 4.6+/-1.6, respectively, which are relatively lower than the reported values in neighboring countries. The mean concentrations (in Bqkg(-1) fresh weight except for tea and grass which is expressed in Bqkg(-1) dry weight) of (137)Cs and (90)Sr are 0.1+/-0.03 and 7.7+/-4.1 in pine needle, 0.27+/-0.05 and 3.0+/-1.1 in tea, 0.65+/-0.19 and 2.1+/-0.3 in grass, 0.033+/-0.021 and 0.084+/-0.045 in wheat, 0.019+/-0.01 and 0.23+/-0.06 in China cabbage, and 0.009+/-0.007 and 0.024+/-0.084 in rice, respectively. The pine needle and tea can be regarded as indicator species for (90)Sr and (137)Cs. The soil-to-plant transfer factor (TF) values of (90)Sr and (137)Cs are, respectively, 0.022 and 0.031 for rice, 0.066 and 3.83 for China cabbage, 0.0088 and 0.089 for wheat, and 0.037 and 0.56 for grass.