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1.
Environ Geochem Health ; 46(8): 270, 2024 Jul 02.
Article in English | MEDLINE | ID: mdl-38954122

ABSTRACT

Radioactive nuclides cesium (Cs) and strontium (Sr) possess long half-lives, with 135Cs at approximately 2.3 million years and 87Sr at about 49 billion years. Their persistent accumulation can result in long-lasting radioactive contamination of soil ecosystems. This study employed geo-accumulation index (Igeo), pollution load index (PLI), potential ecological risk index (PEPI), health risk assessment model (HRA), and Monte Carlo simulation to evaluate the pollution and health risks of Cs and Sr in the surface soil of different functional areas in a typical mining city in China. Positive matrix factorization (PMF) model was used to elucidate the potential sources of Cs and Sr and the respective contribution rates of natural and anthropogenic sources. The findings indicate that soils in the mining area exhibited significantly higher levels of Cs and Sr pollution compared to smelting factory area, agricultural area, and urban residential area. Strontium did not pose a potential ecological risk in any studied functional area. The non-carcinogenic health risk of Sr to the human body in the study area was relatively low. Because of the lack of parameters for Cs, the potential ecological and human health risks of Cs was not calculated. The primary source of Cs in the soil was identified as the parent material from which the soil developed, while Sr mainly originated from associated contamination caused by mining activities. This research provides data for the control of Cs and Sr pollution in the surface soil of mining city.


Subject(s)
Cesium Radioisotopes , Mining , Soil Pollutants, Radioactive , Risk Assessment , China , Soil Pollutants, Radioactive/analysis , Cesium Radioisotopes/analysis , Humans , Strontium Radioisotopes/analysis , Cesium/analysis , Cities , Soil/chemistry , Monte Carlo Method , Radiation Monitoring
2.
Arh Hig Rada Toksikol ; 75(2): 155-158, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38963139

ABSTRACT

The invasion of Ukraine and military operations around Ukrainian nuclear power plants and other nuclear facilities have prompted us to search for radiocaesium in mosses from the Kopacki Rit Nature Park in Croatia, since mosses are known bioindicators of airborne radioactive pollution, and Kopacki Rit is a known low radiocaesium background area. Sampling was finished in August 2023, and our analysis found no elevated radiocaesium levels. Kopacki Rit therefore remains a suitable place for future detection of anthropogenic radioactive pollutants.


Subject(s)
Cesium Radioisotopes , Radiation Monitoring , Croatia , Ukraine , Cesium Radioisotopes/analysis , Radiation Monitoring/methods , Nuclear Power Plants , Air Pollutants, Radioactive/analysis , Humans
3.
PLoS One ; 19(7): e0306531, 2024.
Article in English | MEDLINE | ID: mdl-38954696

ABSTRACT

This paper presents research on the assessment of the radioecological state of plant cover surrounding two research reactor facilities located within the Semipalatinsk Test Site (STS) as examples of nuclear fuel cycle facilities (NFC). Source data on the concentrations of artificial radionuclides in the plant cover were obtained. Quantitative values for 137Cs, 241Am, and 239+240Pu activity concentrations were determined in plants across the perimeters of the facilities, indicating that these compounds may be present in the associated media from the perspective of accumulative bioindication. The values determined for artificial radionuclides in the 'soil‒plant' system around the researched NFC facilities were attributed to radioactive contamination of the STS territory.


Subject(s)
Radiation Monitoring , Radioisotopes , Radiation Monitoring/methods , Radioisotopes/analysis , Plants/chemistry , Plants/metabolism , Soil Pollutants, Radioactive/analysis , Cesium Radioisotopes/analysis , Nuclear Reactors , Nuclear Power Plants
4.
Environ Monit Assess ; 196(8): 709, 2024 Jul 06.
Article in English | MEDLINE | ID: mdl-38970718

ABSTRACT

This article focuses on the study of the distribution of 137Cs in the bottom sediments of Arctic rivers of the Barents Sea basin (using the example of the Nenets Autonomous Okrug, Russian Arctic). This research is relevant due to the poorly studied region and the significant number of radiation-hazardous facilities in the Arctic zone of Russia, both those currently in operation and those that are "nuclear heritage sites". The study of 137Cs specific activity in bottom sediments was carried out in the period from 2020 to 2023 in the rivers Chizha, Nes, Vizhas, Oma, Pechora (river delta), as well as the rivers Kolva and Usa (first and second order tributaries, respectively, of the Pechora River). A total of 199 samples were collected. In addition to 137Cs specific activity, the samples were analysed for sediment particle size distribution, organic matter content, carbonate content and ash content. The 137Cs specific activity mainly ranged from the minimum detectable specific activity to 5.4 ± 0.8 Bq·kg-1. In the Nes River basin (Kaninskaya tundra), the 137Cs content in bottom sediments reached 36.0 ± 3.2 Bq·kg-1 (in the case of lake sediments) and 22.9 ± 3.7 Bq·kg-1 (in the case of river sediments), values that are higher than those of the North-West of Russia. Considering the large area of the study area (Kaninskaya tundra, Pechora river delta, southern part of Bolshezemelskaya tundra) and the similarity of physical and chemical parameters of the studied rivers, it is possible to assume the existence of a zone of increased radionuclide content in the Nes river basin. This may be due to the runoff from the Nes River catchment area, its hydrological features, and the accumulation of 137Cs in the small fractions of bottom sediments. The results confirm the conclusions of previous soil studies in the Nes river basin. The main sources of elevated 137Cs content are global atmospheric deposition and the Chernobyl Nuclear Power Plant accident.


Subject(s)
Cesium Radioisotopes , Geologic Sediments , Radiation Monitoring , Rivers , Water Pollutants, Radioactive , Cesium Radioisotopes/analysis , Rivers/chemistry , Geologic Sediments/chemistry , Water Pollutants, Radioactive/analysis , Russia , Arctic Regions
5.
Environ Geochem Health ; 46(7): 235, 2024 Jun 07.
Article in English | MEDLINE | ID: mdl-38849625

ABSTRACT

In our previous study, the decontamination efficiency of cesium-137 (137Cs) by Napier grass (Pennisetum purpureum Schum.) in the field was shown to be variable and often influenced by natural environmental factors. To elucidate the factors influencing this variable 137Cs-decontamination efficiency, we investigated the influences of soil type and drought stress on Cs accumulation using cesium-133 (133Cs) in Napier grass grown in plastic containers. The experiment was performed using two soil types (Soil A and B) and three different soil moisture conditions: well-watered control (CL), slight drought stress (SD), and moderate drought stress (MD). Overall, our results indicate that soil type and drought have a significant impact on plant growth and 133Cs accumulation in Napier grass. Plant height (PH), tiller number (TN), leaf width (Wleaf), and dry matter weight of aboveground parts (DWabove) and root parts (DWroot) in Soil B were greater than those in Soil A. Drought stress negatively affected chlorophyll fluorescence parameters (maximal quantum efficiency of photosystem (PS) II photochemistry and potential activity of PS II), PH, TN, Wleaf, DWabove, DWroot, and total 133Cs content (TCs), but it had a positive effect on 133Cs concentration. The 133Cs concentration in the aboveground parts (Csabove) was increased by MD approximately 1.62-fold in Soil A and 1.11-fold in Soil B compared to each CL counterpart. The TCs in the aboveground parts (TCsabove) decreased due to drought by approximately 19.9%-39.0% in Soil A and 49.9%-62.7% in Soil B; however, there was no significant effect on TCsabove due to soil type. The results of this study indicate that soil moisture is a key factor in maintaining Napier grass 137Cs-decontamination efficiency.


Subject(s)
Cesium Radioisotopes , Droughts , Pennisetum , Soil Pollutants, Radioactive , Cesium Radioisotopes/metabolism , Soil Pollutants, Radioactive/metabolism , Pennisetum/metabolism , Soil/chemistry
6.
Sci Total Environ ; 945: 173583, 2024 Oct 01.
Article in English | MEDLINE | ID: mdl-38851332

ABSTRACT

Accidental release of radiocaesium (137Cs) from nuclear power plants may result in long-term contamination of environmental and food production systems. Assessment of food chain contamination with 137Cs relies on 137Cs soil-to-plant transfer data and models mainly available for regions affected by the Chornobyl and Fukushima accidents. Similar data and models are lacking for other regions. Such information is needed given the global expansion of nuclear energy. We collected 38 soils worldwide of contrasting parent materials and weathering stages. The soils were spiked with 137Cs and sown with ryegrass in greenhouse conditions. The 137Cs grass-soil concentration ratio varied four orders of magnitude among soils. It was highest in Ferralsols due to the low 137Cs interception potential of kaolinite clay and the low exchangeable potassium in these soils. Our results demonstrate, for the first time, the high plant uptake of 137Cs in tropical soils. The most recent 137Cs transfer model, mainly calibrated to temperate soils dominated by weathered micas, poorly predicts the underlying processes in tropical soils but, due to compensatory effect, still reasonably well predicts 137Cs bioavailability across all soils (R2 = 0.8 on a log-log scale).


Subject(s)
Cesium Radioisotopes , Radiation Monitoring , Soil Pollutants, Radioactive , Soil , Cesium Radioisotopes/analysis , Soil Pollutants, Radioactive/analysis , Soil/chemistry , Radioactive Hazard Release , Lolium
7.
Sci Total Environ ; 945: 174010, 2024 Oct 01.
Article in English | MEDLINE | ID: mdl-38880141

ABSTRACT

Approximately 70 % of the area highly 137Cs-contaminated by the Fukushima Daiichi Nuclear Power Plant accident is forested. Decontamination works in most of these forests have not progressed, and the forestry industry remains stagnant. Although the long-term dynamics of 137Cs in the forest ecosystem will be controlled by the amount of 137Cs absorbed by roots in the future, temporal changes in 137Cs of tree roots have rarely been reported. In the present study, we monitored the depth distribution of 137Cs in the soil and absorptive very fine (VF) roots of 0.5 mm or less in a Japanese cedar forest from 2011 to 2023. As a result, the 137Cs inventory in the mineral soil increased over time due to the migration from the forest canopy and litter layers, whereas that in the VF roots tended to decrease since 2020, although there was a large variation. Temporal decrease in the exchangeable 137Cs fraction with fixation and temporal increase in VF root biomass with their growth were not clearly observed, the 137Cs concentration in the VF roots at 0-2 cm decreased with the decrease in 137Cs concentration in the litter layers. Although the 137Cs concentration in the VF roots below 2 cm tended to increase with increasing 137Cs concentration in the soil at the same depth, the downward migration of 137Cs within the soil can reduce the amount of 137Cs absorbed by roots because the VF root biomass decreases exponentially with depth. In other words, 137Cs can be removed from the long-term active cycles of forest ecosystems as they migrate deeper into the soil. This natural migration process can be regarded as a "self-cleaning" of the forest ecosystem, the green and sustainable remediation using such self-cleaning should be actively adopted for the future forest management.


Subject(s)
Cesium Radioisotopes , Cryptomeria , Forests , Fukushima Nuclear Accident , Plant Roots , Radiation Monitoring , Soil Pollutants, Radioactive , Cesium Radioisotopes/analysis , Soil Pollutants, Radioactive/analysis , Japan , Plant Roots/metabolism
8.
J Environ Radioact ; 277: 107466, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38838510

ABSTRACT

Plutonium, as well as fission products such as 137Cs, had been released into the earth environment in 1945 after the first atmospheric nuclear explosion of plutonium bomb in the desert of New Mexico (USA, July 16) and later over Nagasaki (August 9), followed then by many other explosions. Thus, plutonium cycling in the atmosphere and ocean has become a major public concern as a result of the radiological and chemical toxicity of plutonium. However, plutonium isotopes and 137Cs are important transient tracers of biogeochemical and physical processes in the environment, respectively. In this review, we show that both physical and chemical approaches are needed to comprehensively understand the behaviors of plutonium in the atmosphere and ocean. In the atmosphere, plutonium and 137Cs attach with aerosols; thus, plutonium moves according to physical and chemical processes in connection with aerosols; however, since plutonium is a chemically reactive element, its behavior in an aqueous environment is more complicated, because biogeochemical regulatory factors, in addition to geophysical regulatory factors, must be considered. Meanwhile, 137Cs is chemically inert in aqueous environments. Therefore, the biogeochemical characteristics of plutonium can be elucidated through a comparison with those of 137Cs, which show conservative properties and moves according to physical processes. Finally, we suggest that monitoring of both plutonium and 137Cs can help elucidate geophysical and biogeochemical changes from climate changes.


Subject(s)
Air Pollutants, Radioactive , Atmosphere , Plutonium , Radiation Monitoring , Plutonium/analysis , Atmosphere/chemistry , Air Pollutants, Radioactive/analysis , Water Pollutants, Radioactive/analysis , Cesium Radioisotopes/analysis , Oceans and Seas
9.
Radiat Prot Dosimetry ; 200(10): 901-918, 2024 Jun 22.
Article in English | MEDLINE | ID: mdl-38855829

ABSTRACT

The aim of the study is a thorough investigation of the radioactivity level in soils of the town of Bitola (Macedonia) and its environs. Topsoil samples collected from 58 locations within a 5 × 5 km grid were analysed. Serving as a screening, gross alpha and beta activity measurements were performed using gas-flow proportional counter. Gamma-spectrometric measurements revealed the presence of three natural (40K, 226Ra, 232Th) and one artificial radionuclide (137Cs) in the samples. The activity concentrations of these radionuclides were consistent with the results of similar studies in neighbouring areas. Spatial distribution maps and factor analyses have revealed that the activity concentrations of the natural radionuclides are strongly influenced by geology and have no significant influence from human activities. A correlation of 137Cs activity concentrations with terrain elevation was also observed. The aim of the study is a thorough investigation of the radioactivity level in soils of the town of Bitola (Macedonia) and its environs. Topsoil samples collected from 58 locations within a 5 × 5 km grid were analysed. Serving as a screening, gross alpha and beta activity measurements were performed using gas-flow proportional counter. Gamma-spectrometric measurements revealed the presence of three natural (40K, 226Ra, 232Th) and one artificial radionuclide (137Cs) in the samples. The activity concentrations of these radionuclides were consistent with the results of similar studies in neighbouring areas. Spatial distribution maps and factor analyses have revealed that the activity concentrations of the natural radionuclides are strongly influenced by geology and have no significant influence from human activities. A correlation of 137Cs activity concentrations with terrain elevation was also observed.


Subject(s)
Cesium Radioisotopes , Radiation Monitoring , Radium , Soil Pollutants, Radioactive , Spectrometry, Gamma , Soil Pollutants, Radioactive/analysis , Radiation Monitoring/methods , Radium/analysis , Cesium Radioisotopes/analysis , Potassium Radioisotopes/analysis , Thorium/analysis , Humans , Soil/chemistry , Cities
10.
Environ Monit Assess ; 196(7): 615, 2024 Jun 14.
Article in English | MEDLINE | ID: mdl-38871834

ABSTRACT

The Citarum watershed and the Saguling reservoir are vital natural resources in Indonesia, affecting the livelihood of West Java and the DKI Jakarta population. This study aimed to assess the soil erosion in the Upper Citarum watershed and identify its source. The study used the fallout radionuclide technique, geochemical tracers, and an unmixing model to measure soil erosion and the contribution of suspended sediment sources due to erosion. Soil bulk transects and surface soil were sampled using a coring tool on the Ciwidey and Cisangkuy sub-watersheds. Riverbank and suspended sediment samples were collected from tributaries and rivers. With 137Cs, 40% of the samples had values below the minimum detectable activity, and vice versa for 210Pbex, all samples are detectable. For mitigation, bare land needs to be recovered due to its erosion (25.6 t ha-1 year-1) exceeding the tolerance erosion value (17 t ha-1 year-1). Statistically, Mg and Na were the most appropriate composite tracers for suspended sediment contribution. The unmixing model predicted the sediment contributors from bare land (58%), the riverbank (32.7%), and plantation land (9.3%). Proper land conservation could reduce sediment supply by almost 14.7% and extend the reservoir's life. This is the first study to report the feasibility of the unmixing model in Indonesia.


Subject(s)
Environmental Monitoring , Rivers , Soil Erosion , Indonesia , Environmental Monitoring/methods , Rivers/chemistry , Geologic Sediments/chemistry , Soil/chemistry , Cesium Radioisotopes/analysis , Conservation of Natural Resources/methods
11.
Radiat Prot Dosimetry ; 200(9): 836-841, 2024 Jun 18.
Article in English | MEDLINE | ID: mdl-38836581

ABSTRACT

In previous studies, some of the important factors that affect the spread of radioactive aerosols into indoors were considered. The studies were based on a new CFD approach and provided good descriptions for the deposition of aerosol particles inside small spaces and the penetration of aerosols into buildings through wall cracks. In this article, an application of those studies is implemented, where all the graphical relations that are required to estimate the indoor concentrations of radioactive aerosols from nuclear accidents are provided. This includes the deposition velocities, deposition rate, and the penetration factor. Particular interest is in the Fukushima-Daiichi nuclear power plant accident that took place in Japan in 2011. The aerosols carrying the radioiodine iodine-131 and the radiocesium cesium-134 and cesium-137 are studied. Based on the model's assumptions, and assuming steady-state air concentrations, the radioactive aerosols' concentrations in indoor air are about 97% of the concentrations in outdoor air. The applications demonstrate the model to be convenient and practical.


Subject(s)
Aerosols , Air Pollutants, Radioactive , Air Pollution, Indoor , Cesium Radioisotopes , Fukushima Nuclear Accident , Iodine Radioisotopes , Radiation Monitoring , Aerosols/analysis , Air Pollutants, Radioactive/analysis , Radiation Monitoring/methods , Cesium Radioisotopes/analysis , Iodine Radioisotopes/analysis , Air Pollution, Indoor/analysis , Japan , Humans , Radioactive Hazard Release
12.
J Environ Radioact ; 277: 107458, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38781769

ABSTRACT

The expansion of the nuclear industry has led to various radioactive effluents, originating from routine operations or catastrophic incidents such as those at Three Mile Island (USA), Chernobyl (Ukraine), and Fukushima (Japan). Research conducted after these events emphasizes Cesium-137 (137Cs) and iodine 131 (131I) as major contributors to harmful airborne dispersion and fallout. These isotopes infiltrate the human body via inhalation, ingestion, or wounds, posing significant health risks. Understanding contamination mechanisms and devising effective countermeasures are crucial in mitigating nuclear incident consequences. We propose that concurrent administration of Pru-Decorp™/Pru-Decorp-MG and potassium iodide (KI) could synergistically reduce the levels of 137Cs and block uptake of 131I, respectively, in nuclear incident scenarios. Pru-Decorp™ capsules contain insoluble ferric hexacyanoferrate(II) and are equivalent to USFDA-approved Radiogardase®-Cs, offering radiation exposure mitigation for Cs and Tl contamination. Pru-Decorp-MG capsules consist of insoluble PB and magnesium hydroxide, serving as a prophylactic measure to reduce the risk of internal Cs and Tl contamination for rescue responders. Pru-Decorp™/Pru-Decorp-MG binds Cs/Tl ions in the gastrointestinal tract, hindering absorption and promoting excretion, while KI saturates the thyroid gland with stable iodine, decreasing the uptake of radioactive iodine isotopes. Our hypothesis is supported by studies demonstrating the effectiveness of combination therapies, such as calcium alginate, iron(III) ferrocyanide, and KI, in decreasing the retention of radioisotopes in vital organs. To test this hypothesis, we propose a comprehensive research plan, including in vitro studies simulating gastrointestinal conditions, animal studies to evaluate the efficacy of both drugs simultaneously, and safety clinical trials comparing Pru-Decorp™/Pru-Decorp-MG alone, KI alone, and their combination. Expected outcomes include insights into the synergistic effects of Pru-Decorp™/Pru-Decorp-MG and KI, guiding the development of optimized treatment protocols for simultaneous administration during radioactive contamination incidents. This research aims to address significant critical gaps in nuclear incident preparedness by providing evidence-based recommendations for concurrent antidote use in scenarios involving multiple isotope contamination. Ultimately, this will enhance public health and safety during nuclear emergencies.


Subject(s)
Cesium Radioisotopes , Ferrocyanides , Iodine Radioisotopes , Potassium Iodide , Potassium Iodide/chemistry , Ferrocyanides/chemistry , Cesium Radioisotopes/analysis , Iodine Radioisotopes/analysis , Humans , Radiation Monitoring/methods , Fukushima Nuclear Accident , Radioactive Hazard Release
13.
Chemosphere ; 359: 142273, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38750727

ABSTRACT

This comprehensive review examines recent trends in phytoremediation strategies to address soil radionuclide contamination by cesium (Cs) and strontium (Sr). Radionuclide contamination, resulting from natural processes and nuclear-related activities such as accidents and the operation of nuclear facilities, poses significant risks to the environment and human health. Cs and Sr, prominent radionuclides involved in nuclear accidents, exhibit chemical properties that contribute to their toxicity, including easy uptake, high solubility, and long half-lives. Phytoremediation is emerging as a promising and environmentally friendly approach to mitigate radionuclide contamination by exploiting the ability of plants to extract toxic elements from soil and water. This review focuses specifically on the removal of 90Sr and 137Cs, addressing their health risks and environmental implications. Understanding the mechanisms governing plant uptake of radionuclides is critical and is influenced by factors such as plant species, soil texture, and physicochemical properties. Phytoremediation not only addresses immediate contamination challenges but also provides long-term benefits for ecosystem restoration and sustainable development. By improving soil health, biodiversity, and ecosystem resilience, phytoremediation is in line with global sustainability goals and environmental protection initiatives. This review aims to provide insights into effective strategies for mitigating environmental hazards associated with radionuclide contamination and to highlight the importance of phytoremediation in environmental remediation efforts.


Subject(s)
Biodegradation, Environmental , Cesium Radioisotopes , Soil Pollutants, Radioactive , Strontium Radioisotopes , Strontium Radioisotopes/metabolism , Strontium Radioisotopes/analysis , Soil Pollutants, Radioactive/metabolism , Soil Pollutants, Radioactive/analysis , Cesium Radioisotopes/metabolism , Cesium Radioisotopes/analysis , Soil/chemistry , Plants/metabolism , Strontium/metabolism , Strontium/analysis , Cesium/metabolism
14.
Environ Pollut ; 355: 124213, 2024 Aug 15.
Article in English | MEDLINE | ID: mdl-38795818

ABSTRACT

Although 129I discharge from watersheds is fundamental for assessing long-term radiation effects on aquatic ecosystems, 129I originating from the Fukushima nuclear accident is yet be evaluated. This study investigated the transport behavior of 129I by riverbank surveys conducted from 2013 to 2015 in a watershed where the 129I/137Cs activity ratio is low in the mountainous area and high in the plain as of 2011. Until 2015, the 129I/137Cs activity ratio of the levee crown in the studied watershed was similar to that of the surrounding area in 2011. However, the 129I/137Cs ratios of the surface riverbank sediments were all low, indicating that radionuclides transported from the mountainous area were deposited on the riverbank in the plain. The vertical distribution of the 129I/137Cs ratio in the riverbank sediments indicated that some 129I and 137Cs deposited during the accident remained in the lower layers, but most were eroded immediately after the accident. Based on the 129I/137Cs ratios of sediments deposited on the riverbank, which remained constant until 2015 after the accident, the amount of 129I discharged to the ocean was determined from the previously evaluated 137Cs discharge. It was calculated that 1.8 × 105 Bq and 1.2 × 107 Bq of 129I were discharged with sediment from the studied watershed and the contaminated river watersheds (Abukuma River and Fukushima coastal rivers, including the study river), respectively. This amount of 129I was 0.3% of the 129I released from the Fukushima Dai-ichi Nuclear Power Plant into the ocean immediately after the accident. Furthermore, a comparison of the 129I/137Cs ratio showed that the continuous 129I and 137Cs discharge from the river contribute little to their amount in the seafloor sediments along the Fukushima coast.


Subject(s)
Cesium Radioisotopes , Fukushima Nuclear Accident , Geologic Sediments , Iodine Radioisotopes , Radiation Monitoring , Rivers , Water Pollutants, Radioactive , Rivers/chemistry , Geologic Sediments/chemistry , Water Pollutants, Radioactive/analysis , Japan , Cesium Radioisotopes/analysis , Iodine Radioisotopes/analysis
15.
Sci Total Environ ; 940: 173503, 2024 Aug 25.
Article in English | MEDLINE | ID: mdl-38821276

ABSTRACT

Norway's Centre of Excellence for Environmental Radioactivity (CERAD) research programme included studies on transfer of radionuclides in various ecosystems within the context of environmental risk assessment. This article provides highlights from 10 years of research within this topic and summarises lessons learnt from the process. The scope has been extensive, involving laboratory-based experiments, field studies and the implementation of transfer models quantifying radionuclide uptake directly from the surrounding environment and via food chains. Field studies have had a global span and have, inter alia, covered sites contaminated with radionuclides associated with particles, ranging from nanoparticles to fragments, due to nuclear accidents (e.g., Chornobyl and Fukushima accidents) along with sites having enhanced levels of naturally occurring radioactive materials (e.g., Fen Complex in Norway and Taboshar in Tajikistan). Focus has been put on speciation and kinetics in determining radionuclide behavior and fate as well as on the influence of environmental factors that are potentially critical for the transfer of radionuclides. In particular, seasonal factors have been shown to greatly affect the dynamics of 137Cs and 90Sr bioaccumulation and loss in freshwater fish. The work has led to the collation of organism-specific (i) parameters important for kinetic models, i.e., uptake and depuration rates, and (ii) steady-state concentration ratios, CRs, where the use of stable analogue CRs as proxies for radionuclides has been brought into question. Dynamic models have been developed and applied for radiocaesium transfer to reindeer, radionuclide transfer in Arctic marine systems, transfer to fish via water and feed and commonly used agricultural food-chain transfer models applied in the context of nuclear emergency preparedness. The CERAD programme should contribute substantially to the scientific community's understanding of radionuclide transfer in environmental systems.


Subject(s)
Radioisotopes , Radiation Monitoring , Norway , Ecosystem , Cesium Radioisotopes/analysis , Cesium Radioisotopes/metabolism , Food Chain , Animals , Water Pollutants, Radioactive/analysis , Risk Assessment , Strontium Radioisotopes/analysis , Strontium Radioisotopes/metabolism
16.
J Environ Radioact ; 277: 107450, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38762981

ABSTRACT

In the long-term after atmospheric deposit onto a forest ecosystem, Cs-137 becomes incorporated into the biogeochemical cycle of stable elements and progressively reaches a quasi-equilibrium state. This study aimed at determining to what extent Cs-137 activity distribution in tree vegetation could be predicted from that of stable caesium (Cs-133) and potassium (K), which are known to be stable chemical analogues and competitors for Cs-137 intake in tree organs. Field campaigns that focused on beech trees (Fagus sylvatica L.) were conducted in 2021 in three French forest stands with contrasted characteristics regarding either the contribution of global vs. Chornobyl fallouts, soil or climatic conditions. Decades after Cs-137 fallouts, it was found that more than 80% of the total radioactive inventory in the system remained confined in the top 20 cm mineral layers, while organic layers and beech vegetation (including roots) contributed each to less than 1.5%. The enhanced downward migration of Cs-137 in cambisol than podzol forest sites was presumably due to migration of clay particles and bioturbation. The distribution of Cs-137 and Cs-133 inventories in beech trees was very similar among sites but differed from that of K due a higher accumulation of Cs isotopes in roots (40-50% vs. < 25% for K). The aggregated transfer factor (Tag) of Cs-137 calculated for aerial beech organs were all lower than those reported in literature more than 20 years ago, this suggesting a decrease of bioavailability in soil due to ageing processes. Regarding their variability, Tags were generally lower by a factor 5 at the cambisol site, which was fairly well explained by a much higher value of RIP (radiocesium immobilisation potential). Cs-137 concentrations in trees organs normalized by the soil exchangeable fractions were linearly correlated to those of Cs-133 and the best fit was found for the linear regression model without intercept indicating that no more contribution of the foliar uptake could be observed on long term. Provided that the vertical distribution of caesium concentrations and fine root density are properly measured or estimated, Cs-133 was shown to be a much better proxy than K to estimate the root transfer of Cs-137.


Subject(s)
Cesium Radioisotopes , Fagus , Forests , Radiation Monitoring , Soil Pollutants, Radioactive , Fagus/metabolism , Fagus/chemistry , Soil Pollutants, Radioactive/analysis , Soil Pollutants, Radioactive/metabolism , Cesium Radioisotopes/analysis , Cesium Radioisotopes/metabolism , France , Trees/chemistry , Potassium/analysis , Potassium/metabolism , Chernobyl Nuclear Accident
17.
Environ Geochem Health ; 46(6): 181, 2024 May 02.
Article in English | MEDLINE | ID: mdl-38695964

ABSTRACT

This study determined natural and artificial radionuclide concentrations to evaluate natural radioactivity and health risk levels of nine travertines in the Yaprakhisar and Balkayasi regions in Turkey. The samples coded B1-M, B2, B5, B7, B8, and B10 represent waste derived from the Yaprakhisar travertines, as well as samples T5-M, T12, and Z1 travertines derived from Balkayasi. The levels of natural and artificial radionuclide concentrations (232Th, 40K, and 137Cs) were measured using a high-purity germanium (HpGe) detector system. The travertine activity ranged from 2.09 to 12.07 Bq kg-1 for 232Th, 4.21 to 13.41 Bq kg-1 for 40K, and 0.42-3.26 Bq kg-1 for 137Cs. The results showed that the activity concentration values for 232Th, 40K, and 137Cs were coherent with the travertine analysis results in the UNSCEAR, 2000; 2008 publications. The values obtained were lower than the average values in the UNSEAR reports. The radiological hazard parameters calculated in this study were absorbed gamma dose rate (D), radium equivalent activity (Raeq), annual gonadal dose equivalent (AGDE), exposure dose (ER), total annual effective dose (AEDEtotal), excess lifetime cancer risk (ELCRtotal), gamma representative level (GRL), internal hazard index (Hin) and external hazard index (Hex).


Subject(s)
Cesium Radioisotopes , Potassium Radioisotopes , Radiation Monitoring , Turkey , Radiation Monitoring/methods , Potassium Radioisotopes/analysis , Cesium Radioisotopes/analysis , Thorium/analysis , Soil Pollutants, Radioactive/analysis , Background Radiation , Humans , Risk Assessment
18.
PLoS One ; 19(5): e0303093, 2024.
Article in English | MEDLINE | ID: mdl-38722996

ABSTRACT

Radionuclide contamination is a serious health issue caused by nuclear experiments and plant accidents, as seen for the Chernobyl and Fukushima nuclear plants. Italy has been especially interested in northwestern alpine regions, as have several other nations. The aim of this work was to indagate 134Cs and 137Cs contamination in wild boars, which were considered bioindicators sampled in the Chisone/Germanasca Valley and the Pellice Valley districts (Piedmont, Italy) in two hunting seasons (2014 and 2016). In the 2014 season, only the livers of the animals (n = 48) were sampled, whereas in 2016, five different anatomical sampling sites were sampled for each animal (n = 16). The analyses were conducted in an accredited laboratory (Agenzia Regionale per la Protezione dell'Ambiente-ARPA) by the aid of an HPGe detector (Ortec) with a relative efficiency of 50%. In general, the contamination levels registered in 2014 were under the detection limit for 134Cs and low for 137Cs (Chisone/Germanasca valley: min: 0.0, max: 23.9 median 11.0 Bq/kg vs Pellice valley: min 0, max: 31.7, median: 9.6 Bq/kg) and no health concern can be supposed. In the first-year samples, the liver showed a negative correlation between age and contamination level. In the second year of sampling, low levels were confirmed (min: 3.1 Bq/kg, max: 113.3; median 17.7 Bq/kg). Multiple sampling from the same animal showed that the diaphragm (median = 27.7 Bq/kg) kidney (27.4) and tongue (27.6) were more contaminated than the liver (17.7) and spleen (15.3). Moreover, a linear mixed model revealed a negative organ-by-age interaction, meaning that interorgan differences in contamination level were greater in younger (5-11 months) than in older (18-36 months) animals. Different feeding habits can be the explanation. Our paper shows that muscle sites (diaphragm and tongue) can be useful for radionuclide pollution surveillance in wild boar populations and that younger animals show more interorgan variability in contamination levels than older animals. More investigations are needed to confirm this correlation and to fulfill the request for more data to achieve better risk assessment.


Subject(s)
Cesium Radioisotopes , Sus scrofa , Animals , Cesium Radioisotopes/analysis , Italy , Liver , Radiation Monitoring/methods , Male
19.
J Environ Radioact ; 276: 107439, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38692068

ABSTRACT

Radionuclides from the reactor accident Fukushima Daiichi nuclear power plant were observed in the airborne aerosols at CTBT International Monitoring System (IMS) stations (MRP43, CMP13) in Africa. The maximum activity concentrations in the air measured in Mauritania were 186.44 10-6 Bq.m-3, 264.16 10-6 Bq.m-3 and 1269.94 10-6 Bq.m-3 for 134Cs, 137Cs and 131I respectively, and in Cameroon 16.42 10-6 Bq.m-3, 25.53 10-6 and 37.58 10-6 Bq.m-3 respectively for 134Cs, 137Cs and 131I. The activity ratio of 134Cs/137Cs is almost constant throughout the period of time relevant to this study due to their long half-lives of 30.2 years for 137Cs and 2.06 years for 134Cs. Whereas the 131I/137Cs activity ratio varies in time according to the radioactive decay with a half-live of 8.06 days for 131I and different removal rates of both radionuclides from the atmosphere during transport. The EMAC atmospheric chemistry-general circulation was used to simulate the emission and transport of the isotope 137Cs and map the deposition of the 137Cs deposition over Africa.


Subject(s)
Aerosols , Air Pollutants, Radioactive , Cesium Radioisotopes , Fukushima Nuclear Accident , Radiation Monitoring , Air Pollutants, Radioactive/analysis , Aerosols/analysis , Cesium Radioisotopes/analysis , Atmosphere/chemistry , Iodine Radioisotopes/analysis , Nuclear Power Plants , Africa
20.
J Environ Radioact ; 276: 107443, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38733661

ABSTRACT

To follow up field observations in the Chornobyl Exclusion Zone (ChEZ), a series of controlled model aquarium experiments were conducted to determine the uptake and depuration rates of 137Cs and 90Sr in silver Prussian carp (Carassius gibelio) in fresh water, varying in temperature from 5 to 27 °C, with daily feeding rates of 0-1.5 % fish weight day-1. In the present study, the 137Cs uptake rates in muscle tissues directly from water, 0.05-0.09 day-1 at temperatures of 5-27 °C, were significantly lower than previously reported for fish fed under natural conditions in contaminated lakes within the ChEZ. The rate of 90Sr uptake in bone tissues of silver Prussian carp varied from 0.055 day-1 at a water temperature of 5 °C and feeding rates ≤0.15 % fish weight day-1 to 1.5 ± 0.2 day-1 at a temperature of 27 ± 1 °Ð¡ and at the highest tested feeding rate of 1.5 % day-1. The rate of decrease of 137Cs concentration in muscle tissues was kb = 0.0028 ± 0.0004 day-1 (T1/2 = 248 ± 35 days) at the lowest water temperature tested (5 °Ð¡). At water temperatures between 13 and 26 °Ð¡ and a feeding rate of 0.15 % day-1, the rate increased to kb = 0.0071-0.0092 day-1 (T1/2 = 75-99 days). The rates of decrease of 90Sr activity concentration in bone tissues at water temperatures between 22 and 25 °Ð¡ and a feeding rate of 0.5 % day-1 were kb=0.004-0.0014 day-1, and the associated biological half-life T1/2 ranged 50-160 days, respectively. The present work supported conclusions related to the main pathways of 137Cs and 90Sr uptake by silver Prussian carp, and demonstrated the usefulness of combining field and laboratory uptake and depuration experiments.


Subject(s)
Carps , Cesium Radioisotopes , Radiation Monitoring , Strontium Radioisotopes , Water Pollutants, Radioactive , Animals , Cesium Radioisotopes/metabolism , Cesium Radioisotopes/analysis , Water Pollutants, Radioactive/metabolism , Water Pollutants, Radioactive/analysis , Carps/metabolism , Strontium Radioisotopes/metabolism , Strontium Radioisotopes/analysis
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