Assessment of cancer risk and radiological effects from 210Po and 210Pb with consumption of wild medicinal herbal plants.

BACKGROUND: Plants' raw materials can accumulate chemical elements, including radioisotopes, to some extent and reflect the region they grow in. Due to their high environmental content and toxicity, natural radionuclides - polonium 210Po and lead 210Pb are the most dangerous radioisotopes for human health. METHODS: 70 raw medicinal herbal materials from 54 popular wild-growing medicinal plant species, most of them included in the European Pharmacopoeia, were collected across three regions. In 210 samples, the activity concentrations of 210Po and 210Pb were determined, and their radiotoxicity and cancer risk were calculated. RESULTS: The results of 210Po and 210Pb activities measured in herbal raw material were from 0.12 mBq g-1 dry weight in the fruits of the common chestnut (Aesculus hippocastanum) to 19.7 mBq g-1 dw in herb of ground elder (Aegopodium podagraria) for 210Po, while for 210Pb ranged from 0.16 mBq g-1 dw to 34.3 mBq g-1 dw in the same plants. There were statistically significant differences between 210Po and 210Pb content in leaves, herbs, flowers, and fruit. The studies indicated that the estimated annual effective radiation dose from Polish medicinal herbs consumption was low, ranging 0.03-105 µSv from 210Po and 0.02-98.2 µSv from 210Pb, while the risk of cancer morbidity and mortality ranged from 10-5 to 10-9. CONCLUSIONS: Consumption of the tested medicinal herbs is safe from the radiological point of view and, based on the predictions related to the calculated risk of cancer, should not increase the probability of its occurrence.

The presence of radiotoxic 210Po and 210Pb in Ukrainian wild medicinal plants and the assessment of related dose and cancer risk.

Herbal plants are considered natural pharmaceuticals but also accumulate chemical elements and compounds at high levels. 210Po and 210Pb are highly radiotoxic and may cause carcinogenesis due to ionizing radiation. Thirteen of the most popular wild-growing herbaceous plant species, mostly included in the European Pharmacopoeia, were collected across Ukraine. 210Po and 210Pb were determined in the medicinal plants, and their radiotoxicity and cancer risk were calculated. The results of 210Po activities measured in herbal raw material ranged from 2.28 Bq kg-1 dw (where dw is dry weight) in herb of common horsetail (Equisetum arvense L.) collected near Lviv to 37.7 Bq kg-1 dw in leaves of common birch (Betula pendula Roth.) from Rava Ruska. The activity concentrations of 210Pb varied from 0.44 Bq kg-1 dw in leaves of common birch from Starokostyantyniv to 28.4 Bq kg-1 dw in leaves of common birch from Mizhhirya. There were statistically significant differences between 210Po and 210Pb content in flowers, leaves, and aerial portions. The studies indicated that the estimated annual effective radiation dose from Ukrainian herbs consumption was low, ranging 5.00-82.6 µSv from 210Po and 0.56-35.8 µSv from 210Pb, while the cancer morbidity and mortality risk ranged from 10-4 to 10-6. The presented data indicated no radiological risk related to using herbal plant materials.

210Pb-dating of sediments with models assuming a constant flux: CFCS, CRS, PLUM, and the novel χ-mapping. Review, performance tests, and guidelines.

The 210Pb-based method has been widely used for five decades to determine absolute ages in recent sediments on the centennial scale. Decoding a chronology from the empirical data set requires a series of assumptions that define a mathematical model of the sedimentary conditions. This work aims to provide a comprehensive review of the fundamentals of the existing family of models assuming a constant flux of excess 210Pb at the sediment surface, namely the CFCS, CRS, and PLUM models, and to present the novel χ-mapping versions of the CFCS and CF models. Their performance is assessed with a selected group of five cores from literature data, with varve chronologies or independent time marks. The PLUM model did not produce reliable chronologies in any of the cores studied. The CRS model is too sensitive to an accurate estimation of the total inventory. A weighted-fit and the χ-mapping versions of the CFCS model are prone to over-represent the younger regions of the core. The CFCS model with least squares fitting and the χ-CF models performed best under the most common sedimentary conditions, which involve temporal variability in the fluxes randomly distributed in the time line. A practical strategy is suggested to identify the occurrence of such sedimentary conditions through the combined use of a set of models, providing this way further strength to the 210Pb-dating.

Measurement of Natural Radionuclides and Assessment of Radiation Hazard in Coal from Parts of China.

ABSTRACT: To study the content of radionuclides in coal and to assess its associated radiological impact on the environment for potential radiological risk assessment, a total of 40 coal samples were collected from various mining areas in eight provinces of China. The specific activities of 226Ra, 232Th, 40K, 210Pb, and 238U were measured in all samples using an HPGe gamma-ray spectrometer, and results were compared with available data from other similar studies. The results reveal that the radium equivalent activity was 74.20 Bq kg-1, external hazard index was 0.20, internal hazard index was 0.27, representative gamma index was 0.52, and indoor and outdoor annual effective dose rates were 0.16 nSv y-1 and 0.04 nSv y-1, respectively. Absorbed gamma dose rate in air was 32.87 nGy h-1. In general, these values are lower than the respective threshold limits recommended by UNSCEAR, and the radiation risk to the public is extremely small.

EFFECT OF WORKING CONDITIONS AND NATURAL RADIOACTIVITY LEVELS ON OCCUPATIONAL DOSES TO WORKERS OF AN OLD MANGANESE MINE.

The aim of this work was to use RESRAD-Build model to predict the resulting external and internal radiological doses received by the workers of manganese mine located in Southern Sinai. In order to achieve that goal, measurement of the activity concentrations of natural radionuclides in rock samples collected from the inside gallery of such mine, using hyper pure germanium (HPGe) detector. Radon gas concentrations were also measured. The average activity concentrations of 238U, 226Ra, 232Th, 40K and 210Pb in rock samples were 207.3, 155.5, 59.7, 304.5 and 119.3 Bq kg-1, respectively. The average radon activity concentration was 1254.6 Bqm-3, which is equivalent to 0.135 WL. The radon concentration increases further as going deep inside the mine up to 6238 Bqm-3. RESRAD-Build model occupational effective dose equivalent (EDE) received by the workers, from natural radionuclides, dominated by 222Rn emanated from the parent nuclide 226Ra.There was good agreement between the occupational annual EDE calculated from the measured rock samples and that predicted by modeling, with estimated values of 83.8 and 82.1 mSvy-1, respectively. This radiological dose assessment indicated the predominance of internal pathways owing to radon decay products, in both cases (measured and modeled). The occupational radiological dose from the inhalation of radon and radon decay products resulted in a high lung cancer risk based on the current measurements and ventilation conditions within the mine.

Bolete mushroom Boletus bainiugan from Yunnan as a reflection of the geographical distribution of 210Po, 210Pb and uranium (234U, 235U, 238U) radionuclides, their intake rates and effective exposure doses.

This pioneering study aimed to determine the activity concentrations of 210Po, 210Pb and uranium (234U, 235U, 238U) radionuclides in fruit bodies of wild bolete Boletus bainiugan Dentinger and to estimate its edible safety, which may give scientific evidence for the consumption of this species. The analyses were performed using alpha spectrometer after digestion, exchange resins separation and deposition. Measurement data were analysed and interpolation maps reflecting 210Po, 210Pb and uranium (234U, 235U, 238U) geographical distribution in Yunnan province (China) were presented. In addition, from the perspective of food safety, the possible related effective radiation dose to mushrooms consumers were estimated. The results indicated that 210Po, 210Pb and uranium (234U, 235U, 238U) radionuclides contents in B. bainiugan were significantly different with respect to geographical distribution, and their possible intake in a part of the region was considerably higher. A very interesting observation was done according to the values of 235U/238U activity ratio indicating the occurrence of uranium faction from the global fallout of nuclear weapon tests.

Activity concentrations of 137Cs, 40K, and 210Pb radionuclides in selected medicinal herbs from Central Serbia and their effective dose due to ingestion.

Specific activity of 137Cs, 40K, and 210Pb radionuclides in fifteen selected medicinal herbs from three locations in Central Serbia (two mountains, Kopaonik and Zlatar, and a valley, Sokobanja) was measured using two semiconductor HPGe spectrometer systems. The obtained values are in intervals (<0.3 ÷ 9.7) Bq/kg, (<0.2 ÷ 24.7) Bq/kg, and (<0.2 ÷ 5.7) Bq/kg for 137Cs; in intervals (125 ÷ 1100) Bq/kg, (104 ÷ 872) Bq/kg, and (103 ÷ 954) Bq/kg for 40K, and in intervals (3.6 ÷ 49.0) Bq/kg, (3.9 ÷ 57.9) Bq/kg, and (2.8 ÷ 103) Bq/kg for 210Pb, for herbs from Kopaonik, Sokobanja and Zlatar, respectively. The highest activity measured in individual herbs was: 24.7 Bq/kg for 137Cs (Sokobanja valley), 1100 Bq/kg for 40K (Mt. Kopaonik) and 103 Bq/kg for 210Pb (Mt. Zlatar). The corresponding individual annual effective doses due to ingestion calculated from the measured activity concentrations, of the radionuclides are: in intervals (<1.7 ÷ 82.9) nSv, (<1.4 ÷ 211) nSv, and (<1.1 ÷ 48.7) nSv for 137Cs; in intervals (0.76 ÷ 4.5) µSv, (0.64 ÷ 4.4) µSv, and (0.63 ÷ 4.9) µSv for 40K, and in intervals (1.1 ÷ 18.2) µSv, (1.3 ÷ 21.6) µSv, (0.9 ÷ 38.3) µSv for 210Pb, respectively. The specific activity concentration values of 137Cs and 40K obtained for the investigated herbs are similar to the literature data, while no information was found in literature about specific activity concentration of 210Pb. The all values obtained for individual annual effective dose due to ingestion are less than 100 µSv, which means that the daily use of 200 mL of herbal infusion during a year made from the investigated herbs does not represent a radiological risk for health. However, a high individual annual effective dose of ingestion of 210Pb obtained for some herbs indicate that their consumption in larger amounts 2-3 cups of infusion daily over a year could make the dose to exceed the recommended level, and points to necessity for extensive investigation of 210Pb activity concentration worldwide.

The level of 210Pb extraction efficiency in Polish herbal teas and the possible effective dose to consumers.

The article presents the results of a study on the level of 210Pb efficiency extraction in Polish herbal teas as a possible additional source of this radioactive isotope in the human diet. The twelve most popular herbal teas available in Poland and their infusions in filtered and tap water were analyzed as well as 210Pb activity concentrations and effective doses (radiation) were calculated. The highest activity concentration of 210Pb in dried plants was determined in cistus - 35.5 Bq kg-1 dry wt, while the lowest was in milk thistle - 3.25 Bq kg-1 dry wt what gives respectively for cistus 46.1 ± 0.7 and 6.50 ± 0.29 mBq for milk thistle per one tea bag. The extraction efficiencies in the filtered water oscillated from 5.1 ± 0.5 for milk thistle to 27.3 ± 0.8% for cistus, while for the tap water they ranged from 7.3 ± 0.6% for lime to 33.3 ± 2.2% for white mulberry. Based on the study, it was found that the analyzed herbal tea consumption would give a small portion of the annual effective dose of 210Pb received in Poland - the annual effective radiation dose of 210Pb taken with herbal tea infusions (one glass daily) was calculated from 0.08 ± 0.01 to 3.17 ± 0.08 µSv.

Characterization and radiological impacts assessment of scale TENORM waste produced from oil and natural gas production in Egypt.

This study aims to identify the analytical and radiological characterization of scale TENORM waste produced from oil and natural gas productions in the western desert in Egypt and evaluates their radiological impacts. The mean activity concentration of 238U, 226Ra, 210Pb, 228Ra, 224Ra, and 40K measured in scale TENORM samples is 660 ± 63, 1979 ± 435, 1399 ± 211, 645 ± 104, 794 ± 116, and 556 ± 86 Bq/kg, respectively. Radiological hazard parameters (Raeq, Hex, Hin, etc.) were estimated form the scale TENORM waste sample. All the calculated hazard parameters were found greater than the permissible and recommended safe levels. So the exposure to radiations released from the accumulation of the petroleum scale TENORM waste may cause health risks to the operators and who inhale radioactive radon gases and/or ingest contaminants by radiotoxic nuclides of U, Th, Ra, and Pb. Also, the risks may be extended to the near and/or the general environment.

Naturally occurring radioactive material and risk assessment of tailings of polymetallic and Ra/U mines from legacy sites.

Old mine tailings from Northern and Central Portugal were studied in order to perform a radiological and chemical characterization. The evaluation of massic activity of natural radionuclides and concentrations in tailings of polymetallic and Ra/U mines was performed by gamma spectrometry and neutron activation analysis. Iron speciation was carried out by Mössbauer spectroscopy. In polymetallic tailings with physical ore processing (Cumieira and Verdes - exploited for Sn, Nb-Ta) higher contents of Th, 228Ra and 226Ra in the coarser materials occur, probably due to their presence in host rock and ore fragments. In finer tailings, washing may explain the lower 226Ra and 210Pb massic activity. In tailings with physical/chemical ore processing (Covas - exploited for W and Sn) high U contents and a tendency for higher 226Ra and 210Pb massic activity in the fine materials is observed, probably due to their incorporation in nano-sized particles of iron oxides. A high variation of the 210Pb/226Ra ratio occurs in polymetallic tailings; a deficit of 210Pb can be observed particularly in deposits of settling tanks drained from dumps of chemically treated ore. In Ervideira-Mestras tailings (Ra/U exploitation) where no ore process in situ was performed, a near equilibrium between 210Pb and 226Ra occurs. Dose risk assessment was carried out by calculating external outdoor Annual Effective Dose Rate; the dose rates in air due to terrestrial gamma radiation are low for the polymetallic tailings (<47 nGy/h), and higher for tailings of Ra/U (up to 4130 nGy/h), in the worst scenario.

Comparison of 238U, 210Po and 210Pb Speciation in Six Different Types of Soils.

Speciation of 238U, 210Po and 210Pb in six different types of Syrian soil (Entisols, Inceptisol, Aridisol, Mollisols, Vertisols and Rock outcrops) was studied using a four-step sequential extraction procedure. The binding nature of 238U, 210Po and 210Pb was correlated with soil properties including soil particles, pH, EC, OM, sand, silt and clay. The results showed that the exchangeable and carbonate fractions of 238U did not exceed 10%. In addition, the 238U, 210Po and 210Pb fractions bonded to organic matter increased as the soil clay content decreased. The highest 210Po fraction was found to be bonded to soil Fe/Al/Mn-oxides for Entisols soils (56%) and silica for Aridisol soils (53%). Soil clay content showed a linear correlation with 210Po concentrations in soils ranging from 0.34 to 0.91. The results are considered useful in assessing the risks resulting from soils contaminated by naturally occurring radioactive material from the phosphate and oil industry.

Factors that control the spatial and temporal distributions of phosphorus, nitrogen, and carbon in the sediments of a tropical reservoir.

The impacts of anthropic activities have had profound effects on the nitrogen (N) and phosphorus (P) cycles in many aquatic ecosystems. We investigated the spatial and temporal distributions of carbon (C), N, and P in the sediments of a tropical Paiva Castro Reservoir (São Paulo, Brazil), as well as their release and retention in the system. In 2010, surface sediments were collected at nine sites in the reservoir, and a core was obtained in the limnetic zone, in 2010. The core was dated using the 210Pb technique. The organic C content was estimated from organic matter concentration, which was measured by the loss-on-ignition method, and the concentrations of P and N were determined by spectrophotometry. Marked spatial heterogeneity in the Paiva Castro sediments associated with both natural variations in the water body and variations induced by human impacts was observed. Heterogeneity was evidenced by a decrease in the allochthonous contribution of organic matter (C/N) in the upstream-downstream direction and increases of N and P, mainly associated with water flows in the different compartments of the reservoir. In the core, C and N concentrations display significant positive correlations with increases in population and agricultural activities in the drainage basin through time. The C/P molar ratios in surface sediments are indicative of human impacts in the region, as C:P ratios in the sediment are low (7.8:1) compared to the Redfield ratio (C:P = 108:1). Predominance of oxic conditions at the sediment surface and particles sizes < 63 µm provided favorable conditions for P retention in the sediments, which helps prevent eutrophication. Approaches used in this research should be extended to other locations, especially in mesotrophic and oligotrophic reservoirs, to provide information on historical impacts in such aquatic ecosystems.

Using river sediments to analyze the driving force difference for non-point source pollution dynamics between two scales of watersheds.

The formation and transportation processes of non-point source (NPS) pollution varied among the studied watersheds in the Northeastern China, so we hypothesized that the driving force behind NPS pollution followed the spatial scale effect. With a watershed outlet sedimentary flux analysis and a distributed NPS pollution loading model, we investigated the temporal dynamics of NPS and the differences in driving forces. Sediment core samples were collected from two adjacent watersheds, the smaller Abujiao watershed and the larger Naoli watershed. The natural climatic conditions, long-term variations in the distribution of land use, soil properties and tillage practices were the same in the two watersheds. The vertical distributions of total nitrogen, total phosphorus, Zn and As at 1-cm intervals in the section showed clear differences between the watersheds. There were higher concentrations of total nitrogen and total phosphorus in the larger watershed, but the heavy metals were more concentrated in the smaller watershed. Lead-210 (210Pb) analyses and the constant rate of supply model provided a dated sedimentary flux, which was correlated with the corresponding yearly loading of NPS total nitrogen and total phosphorus in the two watersheds. The total phosphorus showed a stable relationship in both watersheds with an R2 value that ranged from 0.503 to 0.682. A rose figure comparison also demonstrated that the pollutant flux in the sediment was very different in the two watersheds, which had similar territorial conditions and different hydrological patterns. Redundancy analysis further indicated that expanding paddy areas had a large impact on the sedimentary flux of nitrogen and phosphorus in the smaller watershed, but precipitation had a direct impact on NPS loading in the larger watershed. We concluded that the spatial scale effect affected the NPS pollution via the transport processes in the waterway, which was mainly influenced by branch length and drainage density.

RADIONUCLIDE AND MAJOR ELEMENT ANALYSIS OF THERMAL AND MINERAL WATERS IN CROATIA WITH A RELATED DOSE ASSESSMENT.

Major elements concentrations (Na, K, Ca, Mg) and the activity concentrations of 226,228Ra, 234,238U, 210Po, 210Pb, 40K and 137Cs in northern and eastern Croatian thermal and mineral waters, collected directly from springs (or wells), are presented herein with total effective doses assessed for those waters that are considered as drinking 'cures' and are available for consumption. The methods used for radionuclide determination included alpha-particle spectrometry, gas-proportional counting and gamma-ray spectrometry, while the major element composition was determined by ICP-MS. The activity concentrations of all of the radionuclides were found to be below the guidance levels set by the WHO and EC Directive, with the exception of one water sample that measured 0.26 Bq L-1 of 228Ra. The effective ingestion dose assessment for the consumption of the so-called water 'cures' during 1, 2 or 4 weeks' time period throughout 1 year was well below the recommended 0.1 mSv for drinking water.

A REVIEW OF NATURAL RADIONUCLIDES IN CANADIAN DRINKING WATER (1975-16).

Historical results of natural radioactivity in drinking water were reviewed for a total of 21 communities across Canada from 1975 to 2016. Analyses for 226Ra, 210Pb and total uranium were carried out on monthly composite samples of drinking water from selected Canadian municipalities. Generally speaking, levels of 226Ra, 210Pb and total uranium were found to be low compared to national and international standards for drinking water quality. Because levels were low, federal monitoring programs were discontinued in most communities in 1986 except for Regina, Elliot Lake and Port Hope. The population-weighted average levels for these three communities, using data from the most recent 5 years, are <1 mBq/L for 226Ra, <5 mBq/L for 210Pb and <0.4 µg/L for total uranium. The average effective dose resulting from drinking water intake at these levels would be <4.3 µSv per year.

A REVIEW ON VARIATION OF NATURAL RADIOACTIVITY ALONG THE SOUTHEAST COAST OF TAMIL NADU FOR THE PAST 4 DECADES (1974-2016).

This review deals with natural radioactivity variation along the southeast coast of Tamil Nadu for the past four decades (1974-2016). About 40 research works have been conducted along the coast since 1974 in various environmental matrices using a variety of experimental methods. For these measurements researchers are adopted different experimental methods. The measured gamma dose rate ranged from 30 to 8700 nGy/h. The mean specific activity of 238U, 232Th and 40K was found to be 58.8 ± 28.7, 465.2 ± 147.3 and 311.2 ± 27.8 Bq/kg, respectively. The calculated annual exposure rate ranged from 0.29 to 12.8 mSv/y with the mean value of 3.7 mSv/y which is above the global average of 2.4 mSv/y as reported by United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) (Report to General Assembly, Annex B Exposures of the public and workers from various sources of radiation. United Nations, New York (2008)). Plant food items recorded low 210Po activities as compared to seafood organisms. Grain size, season and place of sampling have a decisive bearing on coastal radioactivity. Therefore, it is concluded from the review data that there is an appreciable elevation in background radiation level in the coastal region. This review suggests that new radiological surveys using improved methodology that cover the entire coastal stretch are needed.

Naturally Occurring Radioactive Materials in Uranium-Rich Coals and Associated Coal Combustion Residues from China.

Most coals in China have uranium concentrations up to 3 ppm, yet several coal deposits are known to be enriched in uranium. Naturally occurring radioactive materials (NORM) in these U-rich coals and associated coal combustion residues (CCRs) have not been well characterized. Here we measure NORM (Th, U, 228Ra, 226Ra, and 210Pb) in coals from eight U-rich coal deposits in China and the associated CCRs from one of these deposits. We compared NORM in these U-rich coals and associated CCRs to CCRs collected from the Beijing area and natural loess sediments from northeastern China. We found elevated U concentrations (up to 476 ppm) that correspond to low 232Th/238U and 228Ra/226Ra activity ratios (≪1) in the coal samples. 226Ra and 228Ra activities correlate with 238U and 232Th activities, respectively, and 226Ra activities correlate well with 210Pb activities across all coal samples. We used measured NORM activities and ash yields in coals to model the activities of CCRs from all U-rich coals analyzed in this study. The activities of measured and modeled CCRs derived from U-rich coals exceed the standards for radiation in building materials, particularly for CCRs originating from coals with U > 10 ppm. Since beneficial use of high-U Chinese CCRs in building materials is not a suitable option, careful consideration needs to be taken to limit potential air and water contamination upon disposal of U- and Ra-rich CCRs.

SEISMIC PREDICTION USING UNATTACHED RADON DECAY PRODUCTS.

Long-term measurements of the 222Rn concentration, 222Rn decay product activity, particle size distribution, and unattached, and attached 222Rn decay products, were made at two locations using the 22 y radon decay product 210Pb as their tracer. The particle size sampler collects both short lived 222Rn decay products that ultimately decay to 210Pb on the filters, and also airborne 210Pb. The measurements were made outdoors, at a suburban home and at Fernald, OH, a former uranium processing facility, on top of one of the two 226Ra storage silos containing 150 TBq 226Ra. The size distributions showed the unattached fractions, i.e. particle diameter 2-4 nm, to be 1.5% at the home and 14% at the silos. The unattached fraction of 218Po can be shown to be an immediate measure of the 222Rn concentration. The data indicates detection of the pressure driven 222Rn flow at the silo and with the enhanced measurement capability of a filtered air source versus the usual 222Rn gas measurement. It is proposed that real time measurements of unattached 218Po may be used to identify rapidly changing 222Rn concentrations associated with pressure driven soil air flow associated with seismic activity.

Naturally Occurring Radioactive Material (NORM) in seawater of the northern Arabian Gulf - Baseline measurements.

This study focuses on creating baseline for 238U, 235U, 234U, 210Pb, 210Po and 40K concentrations in the northern Arabian Gulf. The respective concentration ranges were 0.047-0.050, 0.00186-0.00198, 0.054-0.057, 0.00085-0.00092, 0.00051-0.00062 and 18.6-19.1Bql-1. These results suggest that the levels are generally comparable to other marine waters in the northern hemisphere. There were no hot spots observed from oil and gas industry. These data will serve as a baseline to gauge possible future inputs of TENORMs in the northern Gulf. A positive and linear correlation was observed between 238,234U, 40K isotopes and seawater salinity. The results also suggest significant fractionation between 210Po and 210Pb, attributed to rapid removal of 210Po by biota compared to 210Pb. The mean residence time for 210Po in the study area was 371days. The 234U/238U and 238U/235U activity ratios in seawater samples vary between 1.14-1.15, and 0.038-0.040. The 234U/238U and 235U/238U ratio is similar to the expected composition of seawater (1.148±0.002) and 0.0462.

Plant uptake of 238U, 235U, 232Th, 226Ra, 210Pb and 40K from a coal ash and slag disposal site and control soil under field conditions: A preliminary study.

The aim of this study was to investigate the uptake of 238U, 235U, 232Th, 226Ra, 210Pb and 40K by plants that grow on a coal ash and slag disposal site known for its higher content of naturally occurring radionuclides. Plant species that were sampled are common for the Mediterranean flora and can be divided as follows: grasses & herbs, shrubs and trees. To compare the activity concentrations and the resultant concentration ratios of the disposal site with those in natural conditions, we used control data specific for the research area, obtained for plants growing on untreated natural soil. Radionuclide activity concentrations were determined by high resolution gamma-ray spectrometry. Media parameters (pH, electrical conductivity and organic matter content) were also analysed. We confirmed significantly higher activity concentrations of 238U, 235U, 226Ra and 210Pb in ash and slag compared to control soil. However, a significant increase in the radionuclide activity concentration in the disposal site's vegetation was observed only for 226Ra. On the contrary, a significantly smaller activity concentration of 40K in ash and slag had no impact on its activity concentration in plant samples. The calculated plant uptake of 238U, 235U, 226Ra and 210Pb is significantly smaller in comparison with the uptake at the control site, while it is vice versa for 40K. No significant difference was observed between the disposal site and the control site's plant uptake of 232Th. These results can be the foundation for further radioecological assessment of this disposal site but also, globally, they can contribute to a better understanding of nature and long-term management of such disposal sites.