Concentrations Of 238U Research Articles

Disequilibrium in natural decay series in samples from Czech water treatment plants: Uranium, radium and thorium isotopes determination

In the Czech Republic, underground or mixed source water treatment plants are classified as the workplaces with possible increased exposure from a natural source of radiation. When releasing waste materials or residues from these NORM workplaces into the environment, the content of natural radionuclides is measured and compared with the clearance levels established by Czech legislation. The content of natural radionuclides in solid samples is determined primarily by high-resolution gamma-ray spectrometry. Six radionuclides, 238U, 228Th, 226Ra, 228Ra, 210Pb, 40K, are measured directly or by their measurable decay products (assuming equilibrium), the activity concentration of the other four radionuclides, 234U, 230Th, 210Po, 232Th is conservatively estimated. The study is focused on mapping the properties of NORM arising from the treatment of groundwater and, based on the real samples measurement, verification of new proposed assessment approach. It was tested whether the knowledge of the content of natural radionuclides in water can be practically used to estimate the content in NORM. Samples of water, filter material or sludge were taken from 16 different water treatment plants. Combination of gamma-ray spectrometry and radiochemical methods were applied to determine the content of radionuclides 234U, 238U, 226Ra, 228Ra, 228Th, 230Th and 232Th in solid NORM, and radionuclides 234U, 238U, 226Ra, 228Ra in water. Based on the results the proposed modification of the assessment was verified.

Using stable oxygen isotope dual-inlet isotope-ratio mass spectrometry to elucidate uranium transport and mixed 230Th/U calcite formation ages at the seminal Devils Hole, Nevada, natural laboratory.

Vein calcite in Devils Hole has been precipitating continuously in oxygen-isotope equilibrium at a constant temperature for over 500 000years, providing an unmatched δ18O paleoclimate time series. A substantial issue is that coeval calcite (based on matching δ18O values) has uranium-series ages differing by 12 000years. An unparalleled high-accuracy δ18O chronology series from continuously submerged calcite was used to correct the published uranium-series ages of non-continuously formed calcite in two cores, cyclically exposed by water-table decline during glacial-interglacial transitions. This method relies on the premise that the δ18O values of coevally precipitated calcite are identical, allowing matching calcite δ18O values to establish formation ages. Exposed calcite can have apparent ages that are 12 000years too young due to unrecognized uranium mobility and resulting mixed ages identified in over 50 mixed uranium-series ages from previous studies. Secondary uranium in fluids, sourced from the formation or dissolution of porous carbonate deposits (folia) with high uranium-238 (238U) concentrations, has migrated up to 10mm into vein calcite. The continuously submerged Devils Hole δ18O chronology is not explained by orbital forcing. Rather, this chronology represents a regional climate record in the southern Great Basin of sea-surface-temperature (SST) variations off California, variations that preceded the last and penultimate deglaciations by 5000 to approximately 10 000years. Temporal discrepancies between the continuously submerged Devils Hole chronology and other regional δ18O records (e.g., the Leviathan chronology) can be explained by unrecognized cryptic, pernicious uranium mobility, leading to model estimations that may be thousands of years younger than actual ages. Consequently, paleo-moisture availability, water-table, and groundwater recharge models based on these mixed uranium-series ages are too young by as much as 12 000years. The potential for post-formation uranium addition in subaerial cores and speleothems underscores the need for caution in uranium-series dating, highlighting δ18O time-series comparisons as a method for identifying mixed ages.

Environmental assessment of toxic heavy metals and natural radionuclides in irrigation water from Rustenburg, South Africa

Water is a transparent, tasteless and odourless inorganic compound, essential for life and sustainable development. It is important for food and energy production, socio-economic growth, healthy ecosystems and human existence. Global attention is given to water quality monitoring due to the role it plays in human exposure to different kinds of contaminants, including radioactive and toxic contaminants from industrial, agrochemicals, mining and other anthropogenic activities. This work presents the results of measured natural radionuclides and toxic heavy metals in Rustenburg, and their associated non-carcinogenic and carcinogenic risk. The average concentrations of Cd, Cu, Co, Fe, Ni, Mn, Pb and Zn are 0.00007 mg/l, 0.0087 mg/l, 0.0033 mg/l, 0.0636 mg/l, 0.0052 mg/l, 0.0217 mg/l, 0.0003 mg/l and 0.0047 mg/l respectively and are below the safe limit of toxic heavy metals in water. The activity concentration of 40K and 238U ranges from 7.07 Bq/l to 13.2 Bq/l and 1.24 × 10−04 Bq/l to 1.09 × 10−02 Bq/l, with a mean activity concentration of 11.6 Bq/l and 2.78 × 10−03 Bq/l respectively. 232Th was not found in all measured water samples. The estimated average committed effective dose from ingestion of natural radionuclides was observed to be below 170 μSv/yr for 40K, 120 μSv/yr for 232Th and 238U, and a total of 290 μSv/yr reported by the United Nations Scientific Committee on the Effects of Atomic Radiation. The assessment of human health risks resulting from exposure to toxic heavy metals shows negligible carcinogenic and non-carcinogenic health risks to the exposed population, making the water sources from which the sample was collected, safe for agricultural and domestic use. The obtained results will also serve as reference data for future environmental studies.

Activity Concentration of Natural Radionuclides in Surface Sediments of Major River Watersheds in Korea and Assessment of Radiological Hazards

The assessment of potential radiation hazards in accumulated sediments in aquatic ecosystems is vital for the management and disposal of sediments. Furthermore, preemptive management of radionuclides in terrestrial ecosystems is critical for marine ecosystem conservation. We analyzed the activity concentrations of natural radionuclides (226Ra,232Th, 238U, and 40K) in the surface sediments of major river watersheds in Korea and evaluated the radiation hazards stemming from these activity concentrations. The mean activity concentrations of 226Ra and 238U were lower than the global average, whereas those of 232Th and 40K were higher. The mean values of radium equivalent activity, external hazard index, and internal hazard index calculated from these activity concentrations did not exceed the recommended maximum values. The mean values of absorbed gamma dose rate in air and annual outdoor effective dose rate (AEDRout) were higher than the global average by the United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) but remarkably lower than the recommended and background values by the International Commission on Radiological Protection (ICRP) and the Korea Institute of Nuclear Safety (KINS). The contribution of 40K and 232Th to the AEDRout mean value was predominant. In conclusion, the surface sediments of major river watersheds in Korea are associated with negligible radiation hazards. These findings provide fundamental data for the management and treatment of sediments in terrestrial and marine ecosystems.

Assessment of radiological contamination due to gold mining in soil and food crops of Babban Tsauni, Gwagwalada, Nigeria.

This work assessed the activity concentrations of 238U(226Ra), 232Th, and 40K and their associated radiological risks due to exposure to soil and consumption of food crops in Babban Tsauni artisanal gold mine, Gwagwalada, Nigeria, using the gamma spectrometry technique. The mean activity concentrations of 226Ra, 232Th, and 40K in the mine soil were 60.2±9.9, 161.4±16.2, and 664.6±138.2, while they were 46.4±4.9, 79.9±39.3, 266.4±185.4 for tubers and 46.9±15.7, 100.5±35.8, 311.4±132.7 (Bq/kg) for grains, respectively. The results reveal that the activity concentrations of radionuclides in all samples exceeded the recommended values set by United Nations Scientific Committee on the Effects of Atomic Radiation (33, 45, and 420 Bq/kg) except 40K, which fell within the acceptable limit in all food crop sample types. Estimated results for radiological hazard parameters, radium equivalent, annual effective dose due to ingestion, and excess life cancer risk were within safe limits, while the annual effective dose due to external gamma radiation in soil and annual gonadal equivalent dose were significantly high in all investigated samples; these call for constant radiological monitoring.

Estimation of soil-to-plant transfer factor across six local government areas of Kwara state, Nigeria

Transfer factors (TFs) are among the necessary parameter values for the mathematical modeling of radiological pollution's environmental impact. In this study, 238U, 232Th, and 40K activity concentrations and TFs were estimated in 48 soil and plant samples through gamma-ray spectrometry NaI(Tl) in six selected areas of local governments in Kwara State, Nigeria. The findings revealed that the soil and plant samples' 238U and 232Th activity concentrations were within the radiological safety limits. The TFs of soil to plant fell within the worldwide ranges. A set of statistical tests were applied to verify the validity of the data, such as descriptive analysis, the analysis of variance (ANOVA) test, frequency distribution, and Spearman's correlation. The study reveals a skewed distribution in data. Spearman correlation coefficient analysis indicates a moderately negative correlation between 238U, 232Th, and 40K's activity concentrations and their respective TFs (TFU, TFTh, and TFK). In terms of future research in the study area, it is hoped that the data from this study will contribute to improved scientific knowledge.

Uranium isotopes and several heavy elements in selected waters in Quang Nam-Da Nang provinces, Central Vietnam

238U and 234U concentrations, 238U/234U ratios and Na, Ca, Mg, K, Al, As, Cd concentrations were measured in selected surface waters (streams, rivers and lakes), ground waters (dug wells) and underground waters (drill wells and thermal waters) in Quang Nam and Da Nang provinces, Central Vietnam. The mineralization was < 500 mg L−1 and Al, As, Cd contents were a few tenths of µg L−1. 234U and 238U activities were between 0.47–27.6 mBq L−1 and 0.6–15.0 mBq L−1 respectively, these values are lower than WHO recommended limits. Uranium contents trended as Urivers < Ustreams < Ulakes < Udig wells < Uthermal water < Udrill wells. The 234U/238U ratio ranged from 0.69 to 2.31 with 1.26 on average. For groundwaters, the ratio scattered around one. Effects of Nong Son uranium deposit located in Quang Nam region were not observed.

Distribution features of &lt;sup&gt;238&lt;/sup&gt;U, &lt;sup&gt;232&lt;/sup&gt;Th and &lt;sup&gt;226&lt;/sup&gt;Ra in bottom sediments of the shelf and continental slope of Svalbard

The features of the distribution of concentrations of238U,232Th and226Ra in the surface layer of bottom sediments in the bottom sediments of the shelf and continental slope of Svalbard are considered. The content of226Ra,232Th, and238U varied in the range 22–134.3, 22.4–50.9, and 10.9–37.7 Bq/kg, respectively. The amount of226Ra nonequilibrium with238U (226Raex) ranged from 23 to 73% of the total226Ra content in sediments. The maximum concentrations of226Ra,238U,232Th and226Raex(134.3, 37.7, 50.9, and 98.2 Bq/kg, respectively) were obtained in the area of increased bioproductivity (Eagle Trough). In this zone, the relationship between the concentrations of226Ra and226Raexwith the content of organic matter in sediment is well expressed, the correlation coefficients areR= 0.94 and 0.92, respectively, which indicates a significant contribution of the biological community to the accumulation of226Ra in bottom sediments. The226Ra concentration and the226Ra excess value are negatively related to the redox potential of the sediment (R= –0.88). This pattern is also true in other areas of the Svalbard waters. In general, for the entire array of observations, the concentrations of238U and232Th increase with increasing content of organic carbon in the sediment (R= 0.72 and 0.7, respectively). The concentrations of238U and232Th decrease with increasing Ccarbcontent in the sediment (R= –0.79 and –0.81, respectively). The data obtained indicate the need to take into account the226Ra excess when assessing the total natural radioactivity of marine sediments, the value of which may exceed the radioactivity of238U and232Th.

Natural radioactivity and heavy metal contamination in edible fish, shellfish and mollusks at the Bay of Bengal, Kuakata, Bangladesh

In this study, gamma activity concentrations, gross alpha and gross beta activity of natural radionuclides, and heavy metal concentrations were measured in eleven edible marine fish, four shellfish, two mollusks, and a common seaweed sample collected from a local sea fish market and sea beach area of the northern part of the Bay of Bengal, Kuakata, Bangladesh. Using HPGe gamma spectrometry, the activity concentrations of 238U, 232Th, and 40K were measured and found to be 19.7 ± 1.5 Bq/kg, 12.2 ± 0.9 Bq/kg, and 188 ± 15 Bq/kg, respectively, with the 232Th concentration surpassing that of 238U. The ZnS scintillation detector was used to assess the gross alpha and gross beta activity. The average gross alpha activity and gross beta activity were found to be 9.4 ± 1.4 Bq/kg and 26 ± 4 Bq/kg, respectively, with the latter attributed to beta emitting radionuclides's abundance. The activity concentrations of 238U, 232Th, and 40K in the analyzed samples varied in the order of Shellfish > Seaweed > Fish > Mollusks, Seaweed > Shellfish > Mollusks > Fish, and Seaweed > Shellfish > Fish > Mollusks. The annual effective dose due to consumption of analyzed seafood was found to be within the world limit of 2400 μSv/y recommended by UNSCEAR. The main contributor to the annual effective dose was 238U. The excess lifetime cancer risk (ELCR) results were below the permissible threshold of 10−3 for radiological risks. Furthermore, average concentrations of Zn and Mn were higher than WHO/FAO recommended values, and carcinogenic Pb, Cd, Cr, and Hg concentrations were below detection limits, according to heavy metal analysis performed by AAS. The average concentration of heavy metals in all of the seafood samples under investigation was in the order of Zn > Fe > Mn. The calculated hazard index (HI), target hazard quotient (THQ), and estimated daily intake (EDI) were compared to the permissible safety limits.

Radon Gas Detection of Soil Samples in Primary Schools at Najaf City, Iraq

Abstract: The radon concentration, specific activity of 226Ra (CRa), and 238U concentrations (CU) in soil samples from 100 primary schools of Al-Najaf province, Iraq, were measured to determine the safety of students and staff using the CR-39 nuclear track detector based on the sealed can technique. The mean values of 222Rn concentration in the air space of the container (C) and the soil sample (CRn) were 23.53±1.149Bq/m3 and 960.38±47 Bq/m3, respectively. The mean values of CRa and CU were 0.035±0.002 Bq/kg and 0.043±0.002 ppm, respectively. The 222Rn,226Ra, and 238U concentrations were lower than the worldwide level. Radiological parameters such as annual effective dose (AED) and radon exhalation rate per unit mass (EM) and per unit surface (ES) also were determined. The results indicate normal levels for these parameters, except for higher values of AED in some primary schools, according to UNSCEAR data. Keywords: Radon, CR-39 detector, Soil of primary schools, Al-Najaf province.

Dose Measurement and Cancer Risk from Natural Radioactivity in Cleaning Powders at Kurdistan Markets, Iraq

Abstract: The Kurdistan region of Iraq has seen a rise in the use of cleaning powders due to their favorable effects on health. However, various levels of radioactive isotopes, including 238U, 232Th, and 40K, can be found in the ore used to make some cleaning powders. Therefore, washing powder is regarded as one of the environmental sources of radionuclides and radioactivity. In this study, 25 samples of ordinary cleaning powder were analyzed to estimate the specific activities of 238U, 232Th, and 40K using a gamma-ray sodium iodide NaI(Tl) detector. The mean activity concentrations of 238U, 232Th, and 40K were found to be 0.27±0.027, 1.881±0.149, and 19.213±0.899 Bq.kg-1, respectively, which are well below the recommended values set by UNSCEAR 2000: 32, 45, and 400 Bq/kg for 238U, 232Th, and 40K, respectively. The radiological hazard parameters determined for each sample of detergent were also found to be lower than the maximum allowable values recommended by international organizations. Therefore, cleaning powders sold in the Kurdistan region markets pose no radioactive risk to users. Keywords: Cancer risk, NaI(Tl) detector, Detergent, Radioactivity, Primordial radionuclide.

Determination of potentially toxic metals and natural radionuclides in airborne pollens produced different urban environments in Turkey and health risk assessment

ABSTRACT Air pollutants are associated with potentially toxic metals (PTMs) and natural and/or artificial radionuclides, which can pose a major threat to human and environmental health. Pollens can be utilized as a bioindicator to determine the level of air pollution in urban areas. In this study, the concentrations of PTMs and natural radionuclides in 35 airborne pollen samples of 22 species belonging to Pinaceae, Cupressaceae, Araucariaceae, Betulaceae, Salicaceae, and Oleaceae families grown in different urban areas in Turkey were determined using an energy-dispersive X-ray fluorescence spectrometry. For the first time, non-carcinogenic and radiologic health risk assessments for adults were done, estimating hazard index (HI) and annual effective dose (AED), respectively. The concentrations of Fe, Mn, Zn, Ti, Sr, Cu, Ni, Co, Cr, V and Pb analyzed in airborne pollen samples varied from 52.1 to 3078.0, 26.1 to 159.6, 15.6 to 199.7, 9.1 to 282.2, 1.0 to 128.4, 5.0 to 40.1, 5.4 to 23.6, <LD to 11.3, 1.6 to 26.6, <LD to 11.1 and <LD to 5.7 mg/kg, respectively. The average concentrations of K (2%), Th (1.3 mg/kg) and U (1.0 mg/kg) were converted into the activity concentrations (in Bq/kg) of 40K (595.8), 232Th (5.2) and 238U (11.8), respectively. All HI and AED values revealed a very low non-carcinogenic and radiological health risk due to exposure to all PTMs and radionuclides in the pollen samples studied.

Model of U and 226Ra uptake by Spergularia rubra (L.) J. Presl & C. Presl in an area affected by Cu ore mining

Spergularia rubra (L.) J. Presl & C. Presl has a mycorrhizal resistance that leads to increased uranium uptake. The results show that 35% of the 238U is retained in the carbonate fraction and 59% in the residual or non-reactive fraction. 226Ra shows a different pattern with an average association of 19% in the organic matter fraction, 10% in the carbonate compounds and the remaining 71% in the residual fraction. The relationships between the activity concentrations of 238U and 226Ra in the soil fractions and in Spergularia were found to be statistically representative of the carbonate and organic matter fractions, respectively.

Environmental Radiological Impact and Risk Assessment of Natural Radioactivity at the Heap Leach Facility of Tarkwa Goldmine, Ghana: Radiotoxicity and Public Exposure

In this study, a comprehensive investigation was conducted to determine the radioactivity levels of naturally occurring radioactive materials (NORMs) in heap pads/soil and water samples within and around the operational area of Tarkwa Gold Mine in Ghana. Gamma-ray spectrometry was used to determine the activity concentrations of 238U, 232Th, and 40K in heap pads/soil, and 226Ra, 228Th, and 40K in water samples. The average activity concentrations of 226Ra and 228Th in all water samples were below the World Health Organisation (WHO) recommended guidelines for drinking water. Similarly, the average activity concentrations of measured radionuclides in heap pads/soil samples taken from depths of 0–20 cm and 20–50 cm were found to be below the worldwide average reported values. The annual effective dose to the public was estimated to be around 0.16 mSv, which is below the recommended limit. The values of the hazard indices are also below the recommended limits, implying that if heap pads/soils are used for building purposes and construction, they will not pose any significant radiation hazard. The results of this study indicate that radiation levels are within the natural background radiation levels reported in the literature and are consistent with findings from similar studies conducted in Ghana.

Determination of uranium isotopes in ground water by alpha spectrometry and associated age-dependent ingestion dose.

Determination of uranium isotopes in ground water plays a key role in assessment of geochemical condition of ground water and for estimating ingestion dose received by the general public because of uranium intake through drinking water. An attempt has been made in the present study to estimate isotopic composition and activity ratios (AR) of uranium isotopes by analysing the ground water samples using alpha spectrometry. Associated age-dependent ingestion dose was also calculated for the public of different age groups. 238U, 235U and 234U activity concentration was found to vary in the ranges of 5.85±1.19 to 76.67±4.16, < 0.90 to 3.15±0.84 and 6.52±1.25 to 107.02±4.92 mBq/L, respectively. 235U/238U AR varies from 0.038 to 0.068 with an average of 0.047 which is close to 0.046 implies that uranium in the ground water is from natural origin. Uranium concentration was found to vary in the range of 0.47±0.10μg/L to 6.20±0.34μg/L with a mean value of 3.01±0.23μg/L, which is much lower than national as well as international recommendation value. Annual ingestion dose to the public of all age groups for uranium intake through drinking water ranges from 0.60±0.11 to 19.50±1.03μSv/y.

Radioactivity determination in depth distribution of stone samples of Kalaburagi District, Karnataka, India.

The activity concentrations of 238U, 232Th and 40K were found using high-resolution gamma-ray spectrometry on depth profile samples collected from the Kalaburagi districts. This study aims to ascertain the radioactivity Changes concerning the depth profile. With values of 51.64±0.50 Bqkg-1 for 238U, 58.77±0.23 for 232Th and 313.92±3.57 for 40K, respectively, the depth profile samples of Jayanagar in the Kalaburagi region exhibit significant activity concentrations among the measured values. Moreover, estimates of the K/Th and K/U ratios have been made, based on surface-level collected samples, which may have values that differ from the samples under study.

Assessment of radiation dose due to 238U, 226Ra, 222Rn and 210Po in groundwater of Kodagu district, India.

Natural radionuclides are universally spread and can be found in varying levels in rock, soil and water depending on the geology. A potential health threat may be caused by them to humans on consumption of water, food and inhalation of air due to the presence of radionuclides. In the present study, an attempt has been made to study the distribution of 238U, 226Ra, 222Rn and 210Po in groundwater samples of Kodagu district, India. The activity concentrations of 238U, 226Ra, 222Rn and 210Po were found to vary from 0.44 to 8.81μgL-1, 0.71 to 7.66 mBqL-1, 1.54 to 9.61BqL-1 and 0.47 to 4.35 mBqL-1, respectively. The associated dose due to radiation was assessed and was observed to be below the recommended standards. The total effective dose to the population was calculated and was found to be less than the recommended WHO standard of 100mSv.

Apatite Fission-Track Dating: A Comparative Study of Ages Obtained by the Automated Counting LA-ICP-MS and External Detector Methodologies

Abstract Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) in combination with developments in digital microscopy, image analysis, and computer software has allowed the implementation of an automated counting approach for the apatite fission-track (AFT) analysis. We refer to this approach as the “automated counting-LA-ICP-MS” (ACLA) method. Two major components comprise the ACLA method: (i) the digital counting of spontaneous tracks performed on high-resolution images captured from apatite grains and (ii) the measurement of 238U content in apatite by LA-ICP-MS. This study includes ACLA analyses from Fish Canyon Tuff (FCT) and Durango apatite standard crystals. Furthermore, a comparative age study between the ACLA and conventional external detector method (EDM) strategies was performed on a set of thirteen granitoid samples from northwestern Mexico and four granitic samples from the eastern Dharwar craton (EDC), India. ACLA analyses on FCT yielded an AFT age of 28.1 ± 0.6 (1σ) and 28.8 ± 1.1 (1σ) Ma for Durango apatite, whereas reported EDM ages are 27.5 ± 0.5 and 31.4 ± 0.5 Ma, respectively. Calculated AFT ages using the ACLA method from northwestern Mexico samples range from 11.1 ± 1.1 to 42.0 ± 3.6 Ma (EDM ages range from 10.0 ± 0.8 to 54.0 ± 3.0 Ma), whereas AFT ages from the EDC samples range from 147 ± 3.1 to 220.5 ± 12.5 Ma (EDM ages range from 120.9 ± 4.5 to 197.1 ± 19.4 Ma). Based on a statistical comparison with ages previously determined by the conventional EDM on the same samples and considering their 2σ uncertainties, these ages are in good agreement.

Assessment of the level and risk of radioactive hazards in coastal sediments in northern Vietnam

ABSTRACT Radioactivity in coastal sediments in northern Vietnam was examined using data from five sediment cores to assess radioactivity concentrations and radiation risk indices. Radiation risk indices included radium equivalent activity (Raeq), the absorbed dose rate (ADR), the annual effective dose equivalent (AEDE), the activity utilization index (AUI), the external hazard index (Hex), the representative level gamma index (Iγr), and the annual gonadal effective dose rate (AGDE). The radioactivity concentrations of 40K, 232Th, 226Ra, 238U, and 137Cs were 567, 56.1, 35.1, 37.9, and 1.18 Bq/kg, respectively. The average concentrations of 40K, 232Th, 226Ra, and 238U were above the global average at five sites, except for 137Cs, which was low. The Raeq, Hex, and AUI indices were below the recommended values, while the AEDE, ADR, AGDE, and Iγr indices were above the recommended values. Moreover, 40K, 232Th, 226Ra, and 238U had significant impacts on the radiation hazard indices Raeq, ADR, AEDE, Iγr, AUI, Hex, and AGDE. There are three coastal sediment groups on the northern coast of Vietnam: Group 1 has a higher radioactivity and radiation risk index than Group 2 but a lower value than Group 3. Group 3 had the highest radioactivity and radiation risk index. The values of 40K, 232Th, 226Ra, and 238U and the ADR, AUI, Iγr, and AGDE indices in the sediment threaten the living environment.

Adsorption rate of uranium and thorium isotopes in soil and plants grown in a high background radiation area

ABSTRACT An important method for measuring radionuclide activity is alpha spectrometry. Ten soil samples were collected from the studied area. The activity concentrations of 238U and 234U in the collected soil samples ranged between 135 and 218 Bq kg–1 and between 117 and 183 Bq kg–1, respectively. 232Th, 230Th and 228Th activity concentrations ranged between 101 and 339, between 122 and 234 and between 106 and 385 Bq kg–1, respectively. When calculating the amount of radionuclide transport across the food chain, assessment models usually employ a transfer factor. Through root uptake, U and Th are transferred from the soil to food plants. To monitor the movement of radionuclides from the uranium series in diverse environments, it may be possible to use the ratios of uranium and thorium isotopes. Uranium mobility in soil depends on different physicochemical, organic and enzymatic factors and mechanisms. The high mobility of uranium is the main reason for the accumulation of uranium in the soil at root level and the possibility of its transfer to plants. A group of plants were selected that are grown in this area and the population relies on them mainly to meet their food needs. The concentration and transfer factor values of uranium isotopes were the highest in roots as compared with leaves and stems. Uranium in plants accumulates in roots and is then transferred to leaves. The mobility of uranium in plant tissues is constrained because it frequently adsorbs cell wall components. As a result, concentrations are frequently higher in tissues located in lower parts of the plant, with root surfaces having the highest concentrations.