Transport and fate of Fukushima-derived 137Cs and 134Cs in the seawater of the Northwest Pacific in 2015.

To understand the influence of the Fukushima accident on the Northwest Pacific, the distributions and transportations of 134Cs and 137Cs in the seawater in the Northwest Pacific in May and September 2015 were studied. The data showed that the Fukushima-derived 134Cs and 137Cs at some stations can still be distinguished from background level ~ 4 years later. On the whole, the activities of 137Cs and 134Cs in seawater were decreasing from May to Sep 2015. But the increased inventories and the surface activities of 137Cs imply that there has ever been an extra 137Cs from offshore water transported to this study area (from 31° N to 27° N, 145° E to 152.5° E) in May 2015. The average activities of 137Cs in subtropical gyre area in south of KE were the highest and the least were to the east of Luzon Strait in 2015. In vertical direction, 137Cs in subtropical gyre area were mainly distributed at 100 ~ 500 m layer and 137Cs only at 500 m layer in this area showed an increasing trend from May to Sep 2015 which reflects more 137Cs were still penetrating to deeper layer of 500 m from upper water. But they were almost not found below 1000 m layer. It was associated with the subsurface transport of radiocesiums by Northwest Pacific Mode Water (NPMW) and the diffusion of mesoscale eddy. Different distribution characteristics of 137Cs existed between north of KE and south of KE. The low-temperature-low-salinity water mass likely to be the first Oyashio Intrusion was the main factor that resulted in higher 137Cs appearing at the upper 100 m layers in north of KE.

Radiocaesium in mosses from the Kopacki rit Nature Park in Croatia: searching for undeclared releases from nuclear facilities in war-torn Ukraine.

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.

Assessment of radiation in fishes derived from radiocesium in the port of Fukushima Daiichi nuclear power plant.

This study established specialized radiation dose models to evaluate the internal radiation doses derived from 137Cs and 134Cs in fishes in the port of the Fukushima Daiichi Nuclear Power Plant from 2012 to 2023. By August 2018, the activities of 134Cs and 137Cs in fishes decreased at the T1/2 of 176 d and 191 d, respectively. The corresponding mass concentrations were far lower than 1 mg/kg and the chemical toxicity can be negligible. Regarding radiotoxicity, 18,000 Bq/kgfresh weight of 134Cs and 137Cs in grouper Sebastes schlegelii produced 276 µGy/h of radiation dose, which was below the no-effect-dose-rate benchmarks (400 µGy/h). 740,000 Bq/kgfresh weight of 134Cs and 137Cs in greenling Hexagrammos otakii produced 12,600 µGy/h of radiation dose, which was much higher than 400 µGy/h, indicating the possibility of radiation effects. If a person eats these two reported fishes, the resulting committed effective doses for humans are 7.7 µSv and 6.31 mSv, respectively.

Half-century trends of radioactivity in fish from Danish areas of the North Sea, Kattegat, and Baltic Sea.

This work reports comprehensive time-series datasets over the past 50 years for natural (210Po) and anthropogenic (134Cs and 137Cs) radionuclides in three fish species (cod, herring and plaice) from Danish marine areas covering the North Sea, Kattegat, and Baltic Sea. Impact from the global fallout of atmospheric nuclear weapons testing, radioactive discharges from the European nuclear reprocessing plants and release from Chernobyl accident are clearly detected in the fish samples. While 210Po concentrations in each fish species demonstrated comparable levels across the three regions without notable temporal trends, significantly higher median 210Po concentration was observed in the lower trophic level fish, namely herring and plaice, compared to cod. In contrast, 137Cs concentrations in all three species steadily decrease over time after the Chernobyl-attributed peaks in late 1980s in the entire study area, whereas 137Cs always demonstrated higher concentrations in cod than herring and plaice. Our calculated concentration factors (CFs) for 137Cs in this work indicate that the mean CFs for 137Cs over the past 50 years are significantly different across the three species, following the order of cod < herring < plaice. Based on the time-series data, ecological half-lives (Teco) of 137Cs in fish from Danish marine areas were estimated to evaluate the long-term impact of anthropogenic radioactive contamination in different regions. Our results indicate no significant difference in Teco across different fish species, whereas the weighted mean Teco for fish in the Baltic Sea (29.3 ± 3.9 y) is significantly longer than those of the North Sea (9.8 ± 0.9 y) and Kattegat (11.7 ± 1.2 y), reflecting the strong 'memory effect' of the Baltic Sea due to its slow water renewal. However, the dose assessment demonstrates that the contribution of the natural radionuclide 210Po to ingestion dose from fish consumption is 1-2 order of magnitude higher compared to that of 137Cs.

Utilizing low-cost purple coneflower (Echniacea purpurea) marc for competitive sorption of 152+154Eu(III), 60Co(II) and 134Cs(I) radionuclides.

Echinacea purpurea marc (EPM), a residual of echinacea herb after the extraction process, was used as a natural low-cost sorbent for competitive sorption of 152+154Eu(III), 60Co(II) and 134Cs(I) radionuclides. The EPM was ground to prepare it for use in the sorption process. The variables influencing the sorption process were assessed, including pH, contact time, concentrations of metal ions, and temperature. EPM was characterized by different analytical instruments such as FTIR, SEM, XRD, and DTA/TGA. pH 4.0 was selected as the ideal pH value for competitive sorption of the studied ions. Adsorption kinetics data found that the sorption followed a pseudo-second-order model. The adsorption isotherm data was significantly better suited by the Langmuir isotherms in the case of Eu(III) ions while following Freundlich in the case of Co(II) and Cs(I) ions. Positive ΔHo values confirm the endothermic character of metal ion sorption onto EPM. The loading efficiencies of Eu(III), Co(II), and Cs(I) ions in the EPM column were 66.67%, 9.59%, and 4.81%, respectively. The EPM is a cost-effective and efficient separation of Eu(III) ions more than Cs(I) and Co(II) ions. Therefore, in the future, it will be a starting point for the separation of trivalent elements of lanthanide ions.

Development of metal radioactive liquid reference material for proficiency test.

This study developed liquid reference materials containing various metals, to be used for quality assurance of radiation measurements of the most common metallic wastes generated during the operation or decommissioning of nuclear power plants. The liquid reference materials were prepared by assuming the dissolution of stainless-steel using acid and melting of the major metals present in the stainless steel, namely Fe, Ni, Cr, and Mn, along with the standard sources (134Cs, 137Cs, 60Co, 90Sr). The theoretical massic activity of the standard sources added to the samples and the measured reference values of the gamma and beta emitters in the samples were compared, and they showed good agreement within a one-sigma confidence interval (k = 1). Using the developed reference materials, a proficiency test was conducted on three domestic labs, and the results were evaluated using Z-score. While the evaluation results showed good agreement between the reference values and the reported values for 137Cs and 60Co, all participating labs reported lower values than the reference value for 134Cs. For 90Sr, two out of the three labs reported significantly higher values than the reference value. Based on the results of this study, the developed metal radioactive liquid reference material is expected to be registered as certified reference material (CRM) in the future. They will be used as the CRM for measuring and ensuring the quality of radioactive metal waste.

Radiation risk assessment of coastal biota from a quasi-Fukushima hypothetical accident in the Mediterranean Sea.

The occurrence of the February 6, 2023, earthquake in Turkey was the idea of this research to define a Fukushima-like accident scenario in the Akkuyu nuclear reactor and investigate its radiation effects on the coastal organisms of the Mediterranean Sea. The concentration rate (CR), activity concentration in organisms, internal dose, external dose, and total dose rate were estimated using the ERICA Tool from 137Cs, 134Cs and 131I radionuclides. The minimum and maximum radiocesium CR were calculated at 0.063 Bq kg-1 fresh weight (f.w)/Bq kg-1 soil and 4.042 Bq kg-1 (f.w)/Bq kg-1 soil dry weight (d.w). Where this value for 131I ranged from 0.005 to 0.295 Bq kg-1 (f.w)/Bq kg-1 soil. For mammals-large and arthropods, we calculated the significant internal and external dose rates. All of the estimated dose rates were higher than the ICRP's derived consideration reference levels (10 µGy h-1).

Internal organ dose rate conversion coefficients of Japanese macaques to 134Cs,137Cs and 131I†.

The purpose of this study was to estimate the internal dose of radiation in Japanese macaques (aka Nihonzaru or snow monkey) due to the Fukushima nuclear power plant accident. Images of a male Japanese macaque weighing ~10 kg were acquired using a multi-slice computed tomography (CT) scan with a 64-row segment detector. The CT images were used to create voxel phantoms of the bones, bone marrow, brain, eyes, heart, lungs, stomach, liver, spleen, pancreas, kidneys, intestines, bladder, testes, thyroid and miscellaneous tissue. The Particle and Heavy Ion Transport System (PHITS) Monte Carlo code was used to calculate the internal exposure rate conversion factors for 134Cs, 137Cs and 131I isotopes for the created voxel phantoms with a statistical precision higher than 1%. The PHITS-calculated energy deposits were compared with those for rhesus monkeys. The results showed that the fractions of energy deposits for ß-radiation in different organs were almost identical between the two species. For γ-radiation, there was excellent agreement in the self-absorption rate with the approximate curve of the Japanese macaque, with an average deviation of 2%. The maximum deviation of 12% was for the kidney, which has two organs, so the error with the approximate curve is slightly larger due to the energy loss created between organs.

Bioaccumulation and risk assessment of radiocesium in the Northwest Pacific Ocean from Fukushima Dai-ichi Nuclear Power Plant accident.

To understand which biota are more exposed to radionuclides, the bioaccumulation and risk assessment of radiocesium (137Cs and 134Cs) release from FDNPP in the Northwest Pacific Ocean were analyzed using ERICA tools. The activity level was determined by the Japanese Nuclear Regulatory Authority (RNA) in 2013. The data were used as input to the ERICA Tool modeling software to evaluate the accumulation and dose of marine organisms. The highest and lowest accumulate concentration rate were observed in birds (4.78E+02 Bq kg-1/Bq L-1) and the Vascular plant (1.04E+01 Bq kg-1/Bq L-1), respectively. The total dose rate range for the 137Cs and 134Cs ranged between 7.39E-04 and 2.65E+00 µGy h-1 and 4.24E-05 and 2.91E-01 µGy h-1, respectively. There is no considerable risk to the marine biota in the research region since the cumulative dose rates of radiocesium to the chosen species were all less than 10 µGy h-1.

Testing mosses exposed in bags as biointerceptors of airborne radiocaesium after the Fukushima Dai-ichi Nuclear Power Station accident.

Eight years after the Fukushima nuclear accident, mosses exposed in bags were used to investigate their ability to accumulate radiocaesium and therefore to act as biointerceptors of 134Cs and 137Cs in the evacuated area of the Fukushima territory. Bags were filled with 3 widely studied moss species (Sphagnum palustre, Hypnum cupressiforme, and Hypnum plumaeforme) and exposed for 3, 6 or 9 weeks at 5 former residential sites within the Fukushima area and, for comparison, at three background sites located 700 km away. The radiocaesium activity concentrations found in moss bags were evaluated as function of exposure time, site conditions and moss species. In the Fukushima area, the moss bags accumulated 137Cs at all exposure sites and in all exposure periods, with S. palustre having the highest 137Cs accumulation ability. The 137Cs activity concentrations (from 28 to 4700 Bq kg-1) measured in moss bags increased with the exposure time and were consistent with the decontamination status of each exposure site, highlighting the big potential of moss bags to discriminate among exposure sites. Time dependency of 137Cs activity concentrations measured in mosses allowed the calculation of location-specific and species-specific factors, which can be used to predict radiocaesium accumulation trends in future biomonitoring surveys performed in the same area with the same experimental design. Autoradiography and electron microscopy analyses of the moss surfaces revealed a prevalence of soil-derived particulate form of radiocaesium, suggesting the use of moss bags as warning sensors of resuspended particles potentially harmful for local residents.

Comment on "Development of a gamma ray dose rate calculation and mapping tool for Lagrangian marine nuclear emergency response models" by Little et al.

Care must be taken when calculating the sum of released amounts to the environment for different radionuclides of whose physical and chemical characteristics are quite different and the radiological impact of the radionuclides are also quite different. In this comment, the mishandling of summation in "Development of a gamma ray dose rate calculation and mapping tool for Lagrangian marine nuclear emergency response models by Little et al." is pointed out and the correct way is suggested.

Doses from external irradiation and ingestion of 134Cs, 137Cs and 90Sr of the population of Belarus accumulated over 35 years after the Chernobyl accident.

This study considers the exposure of the population of the most contaminated Gomel and Mogilev Oblasts in Belarus to prolonged sources of irradiation resulting from the Chernobyl accident. Dose reconstruction methods were developed and applied in this study to estimate the red bone-marrow doses (RBMs) from (i) external irradiation from gamma-emitting radionuclides deposited on the ground and (ii) 134Cs, 137Cs and 90Sr ingestion with locally produced foodstuffs. The mean population-weighted RBM doses accumulated during 35 years after the Chernobyl accident were 12 and 5.7 mGy for adult residents in Gomel and Mogilev Oblasts, respectively, while doses for youngest age groups were 20-40% lower. The highest mean area-specific RBM doses for adults accumulated in 1986-2021 were 63, 56 and 46 mGy in Narovlya, Vetka and Korma raions in Gomel Oblast, respectively. For most areas, external irradiation was the predominant pathway of exposure (60-70% from the total dose), except for areas with an extremely high aggregated 137Cs soil to cow's milk transfer coefficient (≥ 5.0 Bq L-1 per kBq m-2), where the contribution of 134Cs and 137Cs ingestion to the total RBM dose was more than 70%. The contribution of 90Sr intake to the total RBM dose did not exceed 4% for adults and 10% for newborns in most raion in Gomel and Mogilev Oblasts. The validity of the doses estimated in this study was assessed by comparison with doses obtained from measurements by thermoluminescence dosimeters and whole-body counters done in 1987-2015. The methodology developed in this study can be used to calculate doses to target organs other than RBM such as thyroid and breast doses. The age-dependent and population-weighted doses estimated in this study are useful for ecological epidemiological studies, for projection of radiation risk, and for justification of analytical epidemiological studies in populations exposed to Chernobyl fallout.

Fukushima-derived radiocesium in the western subarctic area of the North Pacific Ocean, Bering Sea, and Arctic Ocean in 2019 and 2020.

We measured dissolved radiocesium (134Cs and 137Cs) in surface seawater collected in the western subarctic area of the North Pacific Ocean, Bering Sea, and Arctic Ocean in 2019 and 2020. The radiocesium released from the accident of the Fukushima Dai-ichi nuclear power plant (FNPP1) in 2011 was still observed in these areas (∼2 Bq m-3 decay-corrected to the date of the accident). In 2019/2020, the FNPP1-derived radiocesium concentrations in the Bering Sea and the Chukchi Sea, which is a marginal sea of the Arctic Ocean connecting the Bering Sea to the Arctic Ocean, were within the range of those observed in 2017/2018. On the other hand, the FNPP1-derived radiocesium was detected in the Arctic Ocean farther north of the Chukchi Sea in 2019/2020 for the first time. This was probably derived from the long-range transport of the FNPP1-derived radiocesium from the North Pacific coastal area of Japan to the Arctic Ocean through the Bering Sea during the past decade. The transport of the FNPP1-derived radiocesium from the Bering Sea to the western subarctic area in 2019/2020 is not clear, which implies the retainment of the FNPP1-derived radiocesium within the Bering Sea.

Updated soil to fruit concentration ratios for radiocaesium compiled under the IAEA MODARIA II Programme.

Under the International Atomic Energy Agency (IAEA) Modelling and Data for Radiological Impact Assessments (MODARIA II) Programme, Working Group 4 activities included collating radionuclide transfer data from Japan following the Fukushima Daiichi Nuclear Power Plant accident and separately collating concentration ratio (CR) data for root uptake of radionuclides by crops grown in tropical and arid climates. In this paper, the newly compiled radiocaesium CR data for fruit from Japan, tropical and arid climates have been combined with the data originally compiled for the IAEA Technical Reports Series No. 472 (TRS 472) and additional data identified from the literature to produce an enhanced MODARIA II dataset of fruit radiocaesium CR values. Statistical analysis of the MODARIA II dataset by climate class (based on the Köppen-Geiger climate classification) indicated that the CR values for tropical climates were significantly higher (p< 0.05) than those for arid, temperate and cold climates. Statistical analysis of the MODARIA II dataset by soil group (based on soil texture) indicated that the CR values for coral sand soil (tropical climates only) and organic soil (temperate climates only) were significantly higher (p< 0.05) than those for the clay, loam and sand soil groups. Statistical analysis of the MODARIA II dataset by plant group (based on plant morphology) indicated that the CR values for non-woody trees (tropical climate bias) were significantly higher (p< 0.05) than those for herbaceous plants, shrubs and woody trees. Comparison of the MODARIA II dataset with original TRS 472 values showed only small changes in the fruit radiocaesium CR values for herbaceous plants and shrubs in temperate climates. There was a decrease in the CR values for woody trees in temperate climate across all soil groups. There was also a decrease in the CR values for tropical climates for all comparable soil groups.

Fukushima-derived radiocesium in the waters of the Northwest Pacific Ocean in the winter of 2011.

To understand the transport of Fukushima Dai-ichi Nuclear Power Plant Accident (FDNPPA)-derived nuclear contaminated water, which will be discharged into the Pacific Ocean in the future, the distributions of 134Cs and 137Cs in seawater in the public areas east of Japan in winter 2011 were reported in this study. The ranges of 134Cs and 137Cs activities were

Intrusion of Fukushima-derived radiocesium into the East China sea and the Northeast South China Sea in 2011-2015.

To investigate the potential long-term impact of the Fukushima Dai-ichi Nuclear Power Plant Accident (FDNPPA) on the South China Sea (SCS) and the East China Sea (ECS), radiocesium isotopes 134Cs and 137Cs in seawater from 2011 to 2015 were measured. The highest activities of 134Cs and 137Cs in seawater were 0.73 Bq/m3 and 3.34 Bq/m3, respectively. The results demonstrated that FDNPPA-derived radiocesium intruded into the Northeast SCS and the ECS in 2013 and reached a maximum in 2014. The intrusion occurred within the upper 100 m and contributed ≤72.5% of the total 137Cs in the seawater of the SCS and ECS. The formation, subduction, and transport of subtropical mode water (STMW)/central mode water (CMW) trapped FDNPPA-derived radiocesium in the ocean interior and transported it southwestward from the high-latitude open ocean to the low-latitude western boundary area. Then, the FDNPPA-derived radiocesium entered the Northeast SCS and the ECS by the intrusion of the subsurface high-salinity water of the Kuroshio Current into the Northeast SCS and the ECS.

An experimental approach to assess the post-depositional mobility of 134Cs.

The partitioning coefficient, Kd, which is defined by the reversible sorption processes between a solid and an aqueous phase at equilibrium, is one of the most important parameters to assess environmental transport and risk. In this study, a series of simple laboratory experiments were conducted to investigate sorption properties of 134Cs on a model sediment under two treatments (shaken vs non-shaken) and with three (small: <75 µm, large: > 75 µm and bulk i.e., composite) particle size fractions. Vertical transport of 134Cs across the water-sediment interface and into sediment was also evaluated. As expected, grain size had the strongest influence on 134Cs Kd values, with the small particle size fraction yielding significantly higher Kd values than the large and bulk fractions. The mean Kd values obtained from the various experiments ranged from 89 ± 13-130 ± 5 L kg-1 (small), 44 ± 10-91 ± 13 L kg-1 (large), 73 ± 3-112 ± 11 L kg-1 (bulk, shaken) and 73 ± 5-110 ± 4 L kg-1 (bulk, non-shaken). Most of the 134Cs partitioning processes occurred rapidly (<2 h) into the experiment. Physical mixing (shaken) did not appear to significantly affect the 134Cs Kd values. In complement, a separate experiment on the vertical penetration of 134Cs into a bulk sediment column showed that 134Cs was able to penetrate up to 5 cm into the sediment column after 88 days (∼0.6 mm d-1) and this flux rate is comparable to natural settings. Adsorption and contact time were found to be key for the 134Cs penetration process. Results from these experiments add to the literature on post-event radionuclide transport studies in marine settings and provide an experimental perspective that can be built upon to complement field observations.

Concentration of 7Be, 210Pb, 40K, 137Cs, 134Cs radionuclides in the ground layer of the atmosphere in the polar (Hornsund, Spitsbergen) and mid-latitudes (Otwock-Swider, Poland) regions.

This paper presents results of measurements of selected gamma-radioactive radionuclide concentrations (7Be, 210Pb, 40K, 137Cs, 134Cs) in atmospheric aerosols registered in 2002-2017 at the Polish Polar Station of the Institute of Geophysics Polish Academy of Science in Hornsund and in the S. Kalinowski's Geophysical Observatory Institute of Geophysics Polish Academy of Science in Swider. The above measurements and tests are used to control and track long-term concentrations of radionuclides depending on the geometeorological conditions prevailing in the vicinity of the station. Collecting radiological data from polar regions and comparing them with data from medium latitudes leads to a better understanding of the mechanisms of creation and propagation of radionuclides in the air. Hornsund station is one of the northernmost measuring site for continuous airborne radionuclide monitoring in the Spitsbergen archipelago. It also allows the analysis of the relationship of radionuclides to the Earth's magnetic field.

Radioactive impacts of the Fukushima Dai-ichi Nuclear Power Plant Accident on blue sharks in the Northwest Pacific.

The Fukushima Dai-ichi Nuclear Power Plant Accident (FDNPPA) derived 134Cs, 137Cs and 110mAg in blue sharks captured in the Northwest Pacific during 2011-2018 were assessed for the first time in the aspects of radioactive contamination, temporal variation, maternal-to-fetus transfer, tissue distribution and radiation dose, to demonstrate the impacts of the FDNPPA on blue sharks. The contribution of the FDNPPA derived radiocesium in blue sharks (>52%) was estimated based on 134Cs/137Csactivity ratios. The effective and ecological half-lives of the FDNPPA derived 134Cs (270 d, 410 d), and 137Cs (430 d, 450 d) were calculated. These contaminations decreased with time and returned to the level before the FDNPPA during the period of Sep. 2017-Sep. 2018.134Cs and 137Cs tended to distribute in muscles, while 110mAg mainly distribute in their guts. 134Cs and 137Cs were also transferred to fetuses and the activities were up to ~30% of the maternal activities. Dose assessment demonstrated that the highest FDNPPA derived dose rate in blue sharks (~0.42 nGy/h) was far below the ERICA ecosystem screening benchmark of 10 µGy/h and the committed effective dose in humans from ingesting blue shark meat (0.06-0.90 µSv) was far less than that from annual consumption of food and water. It was far from causing radiation harm to blue sharks and humans, suggesting that the impacts of the FDNPPA on blue sharks were not significant.

Safety and efficacy of a feed additive consisting of ferric (III) ammonium hexacyanoferrate (II) for ruminants (domestic and wild), calves prior the start of rumination, lambs prior the start of rumination, kids prior the start of rumination and pigs (domestic and wild) (Honeywell Specialty Chemicals Seelze GmbH).

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the safety and efficacy of ferric (III) ammonium hexacyanoferrate (II) as technological feed additive for ruminants (domestic and wild), calves prior the start of rumination, lambs prior the start of rumination, kids prior the start of rumination and pigs (domestic and wild). The additive is already authorised for use in ruminants (domestic and wild), calves prior the start of rumination, lambs prior the start of rumination, kids prior the start of rumination and pigs (domestic and wild). The additive is effective at the minimum recommended concentration of 50 mg/kg complete feedingstuffs (corresponding to about 10 mg/10 kg bw) in reducing the contamination of food derived from ruminants (domestic and wild), calves, lambs and kids prior to the start of rumination, and pigs (domestic and wild) by caesium. Considering the scarce information available, the Panel is not in the position to conclude on the safety of the additive for the target species. The use of ferric (III) ammonium hexacyanoferrate (II) in feed for ruminants, calves, lambs, kids and pigs at the maximum recommended concentration of 500 mg/kg feed (corresponding to about 150 mg ferric (III) ammonium hexacyanoferrate (II)/10 kg bw) is safe for the consumer. In the absence of data, the Panel is not in the position to conclude on the safety of the additive for the user. The use of ferric (III) ammonium hexacyanoferrate (II) as a feed additive is considered safe for the environment.