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In August 2023, the long-planned discharging of radioactive wastewater from the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) started after the confirmation of its feasibility and safety. As this water contains elevated amounts of tritium even after being diluted, a lot of resources have been invested in the monitoring of the Fukushima coastal region where the discharge outlet is located. We compare the first 3H surface activity concentrations from these measurements (up to the end of November 2023) with the available background values to evaluate a possible impact of the long-term discharging on humans and environmental levels of the radionuclide of interest in the same or nearby area. From our results, we can conclude that the joint effect of horizontal and vertical mixing has been significant enough to reduce tritium concentrations at the monitored locations in the region close to the FDNPP port two days after the end of the respective phase of the discharging beyond the detection limit of the applied analytical methods (∼0.3 Bq L-1) which is by five orders of magnitude lower than safety limit for drinking water set by the World Health Organization (WHO). Moreover, the distant correlation analysis showed that tritium concentrations at stations located further than 1.4 km were very close to pre-discharge levels (∼0.4 Bq L-1). We also estimated that the 3H activity concentration in the offshore Fukushima region would be elevated by 0.01 Bq L-1 at maximum over a year of continuous discharging, which is in concordance with the already published modeling papers and much less than the impact of the FDNPP accident in 2011.

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Radiocarbon measurements of total carbon (TC) fraction of aerosol samples collected at the campus of the Comenius University in Bratislava (Slovakia) during 2022-2023 were carried out. Based on radiocarbon activity of these samples and a source apportionment model we have determined the relative proportion of fossil and non-fossil carbon in collected atmospheric aerosols. The carbon from non-fossil sources (biomass burning and biogenic emissions) was dominant in this time period, on average it formed 72% of carbon present in the aerosols from the atmosphere of Bratislava. The whole range of determined non-fossil fraction was relatively small as it varied only from 0.67 (August-September) to 0.82 (December-January). These changes do not exhibit any significant seasonal variation as was previously observed in Bratislava during 2017-2018 in the elemental carbon (EC) aerosol fraction.

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Deep-ocean sediments, similarly to seawater, are important reservoirs of 137Cs, an anthropogenic radionuclide with a relatively long half-live found in the Earth system. To better understand the geochemical behaviour of 137Cs in the ocean, we examined the temporal changes of 137Cs activity concentrations in the overlying waters and in sediments from the Far Eastern Seas (Sea of Japan, SOJ, and Okhotsk Sea, OS) during the period of 1998-2021. The 137Cs activity levels showed exponential changes during the observed period. The decay-corrected change rates of 137Cs in deep waters of SOJ exhibited a slow increase, while 137Cs levels in seawater and sediment in OS decreased gradually. This reflects a topographical difference, as SOJ is a semi-closed sea, whereas OS receives continuously inflow of subarctic waters. It was confirmed that 137Cs released after the Fukushima Dai-ichi Nuclear Power Plant accident was rapidly transported into the deep waters of the SOJ. To elucidate the transfer processes of 137Cs from seawater to sediment, we discussed the temporal changes of the partition coefficients (Kd) of 137Cs between the overlying water and the surface sediment. In shallow areas (< 1500 m water depth), Kd values were almost constant within the sampling periods, although the temporal changes in the Kd values occurred in deeper waters (> 2500 m depth). The Kd values increased with increasing depth, which may reflect a pressure effect as a possible mechanism. These findings suggest that chemical processes may be important factors controlling the transport of 137Cs between seawater and sediment, although more complicated phenomena occurred in deep waters and sediments of the SOJ (> 3000 m depth).

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The investigation of the impact of the Fukushima accident is still going on although more than ten years have passed since the disaster. The main goal of this paper was to summarize the results of tritium and radiocarbon determinations in different environmental samples, possibly connected with the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident. A document containing compiled data may serve as a solid basis for further research in the selected fields. To accomplish such effort, we went through dozens of relevant published papers, reporting 3H and 14C activity concentrations in precipitations, groundwater, seawater, river systems, tree rings, and, in some more extraordinary samples, such as herbaceous plants or debris from the damaged reactor buildings. As the referenced results would not be obtainable without adequate analytical techniques, the most common methods for routine measurement of tritium and radiocarbon concentrations are discussed as well. We believe that the correct identification of the affected environmental compartments could help quantify the released 3H and 14C activities and track their following fate, which could be especially important for plans to discharge contaminated water from the FDNPP in the upcoming years.

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PURPOSE: We investigated iron accumulation and the possible mechanisms in the rabbit cerebellum after the exposure to the real GSM and generated radiofrequency electromagnetic fields (RF EMF) using inductively coupled plasma mass spectrometry (ICP MS) and particles induced X-ray emission (PIXE). MATERIALS AND METHODS: Four groups of rabbits were exposed to the real EMF, generated EMF, combination of both the real and generated signals and the control group with no exposition. For determination of iron concentration in the four groups of cerebellum samples ICP MS was used. Iron accumulation in samples by PIXE analysis using the 3 MeV proton beam was carried out. RESULTS: Iron concentration measured by ICP MS revealed no significant differences for all the groups. PIXE results showed a focal accumulation of iron with the size up to 3 mm. Highest concentration of iron after exposure to real signal was observed. CONCLUSION: We suggest that the iron accumulation after the exposure to RF ELF is not the result of higher permeability of blood-brain barrier and leaking out of iron from the bloodstream into the brain cells and tissues. It could be the result of an iron actuation and its redistribution in the tissue (Fig. 2, Ref. 86).

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Organic inclusions in lime binders provide useful samples for radiocarbon dating of historical objects. Two Czech castles Týrov and Pysolec from Late Middle Ages were explored, and tens of charcoals were found in their walls. The radiocarbon content of the charcoals was measured with accelerator mass spectrometry. The dating results showed that none of the charcoals were younger than the known historical ages (Týrov: 1260 - 1270, Pysolec: 1300 - 1340), but some were considerably older. Two charcoals from Pysolec castle dated to Palaeolithic, likely originating from fluvial sediments added as an aggregate to the mortar. When excluding these two charcoals, the others indicated most likely dates being 50-100 y older than the building dates of the castles. This systemic effect corresponds to the age of wood used for lime burning and shall be accounted for when dating mortars using charcoals.

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The scientific interest in radiocesium and plutonium found in the oceans and seas has increased enormously in the past years as a consequence of the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident and is expected to be ongoing due to many unresolved questions. Hence, continuous development of new and verification of old analytical methods should be at the top of the list of the community, working on the topic. In this study, we processed and analyzed several seawater samples, collected in different time frames (2011-2015) from the North Pacific Ocean offshore Fukushima, to determine their radiocesium activities, 134Cs/137Cs activity ratios and 240Pu/239Pu isotopic ratios using the sequential scavenging method, gamma spectrometry and accelerator mass spectrometry (AMS). The observed radiocesium levels in seawater (0.07-0.042 Bq L-1) clearly indicated that the investigated region remained impacted by releases from the damaged power plant even after four years after the accident. Regarding plutonium, its successful separation from large volume seawater samples was confirmed by detection of 240Pu by AMS. However, several problems emerged during the analyzes, which we tried to address with the use of additional methods (e.g., measurements of uranium by ICPMS). The efficiencies of the applied methods and other issues are also discussed.

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In March 2011, severe nuclear accident happened at the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) after the gigantic earthquake and following huge tsunami wave. A lot of investigations to assess environmental and radiological impacts of released radionuclides have been conducted by domestic and international organizations. Environmental radioactivity research related to the FDNPP accident has spread widely over different scientific fields due to specific features of the accident, and specifically its impact on the marine environment. The present paper summarizes major lessons learned from the environmental investigations of the FDNPP accident. Environmental radioactivity studies have typical interdisciplinary character; especially physics and chemistry are fundamental as a base of process studies in the environment. In this sight, we review chemical aspects regarding FDNPP-derived radiocesium transfer within and between compartments (atmosphere, ocean and land). We also discuss future trends in investigations of behavior of anthropogenic radionuclides in the environment, important not only for a better understanding of impacts of the FDNPP accident on the environment, but also for improving our general knowledge of the total environment in the Anthropocene era and its protection for the future.

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Distribution trends and temporal variations of 241Am and Pu isotopes in the south-eastern Baltic Sea during the study period of 1999-2001 and 2011-2015 were investigated with the aim to study temporal changes of radionuclide levels in seawater, suspended particles and sediment, to estimate 241Am and 239,240Pu levels in marine biota and to assess the radiation doses received by the biota. The activities of 241Am and 239,240Pu were measured by alpha spectrometry after radiochemical purification. 241Pu was determined radiometrically via the ingrown daughter 241Am after 10-12 years of storage, while the 240Pu/239Pu atom ratio of was measured by accelerator mass spectrometry. The 239,240Pu activities in suspended particles collected in the coastal waters of the Baltic Sea decreased by a factor of ∼3 during the study period, while they decreased about fourfold in the Curonian Lagoon. This could indicate a decrease in the influx of particles containing Pu isotopes into the Baltic Sea. While in the Curonian Lagoon, the 239,240Pu activities in the sediment samples varied insignificantly during the study periods, in the Baltic Sea, the maximum activity decreased by a factor of 6, and the mean/median values decreased by ∼4 times. The assessment tool ERICA was used to calculate the dose rates for biota. The total dose rate from all analysed radionuclides was <0.1 µGy/h, therefore no risk to organisms was identified.

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Long-term temporal variations of plutonium in Sea of Japan (SOJ) surface waters have been examined with the aim to better understand its behavior during several decades. The first observation is that 239,240Pu activity concentrations in surface waters of the SOJ during 1977-2019 were 6.5 ± 4.7 mBq m-3 in average, and 5.1 mBq m-3 as the median, whereas 137Cs and 90Sr activity concentrations decreased with time, except of the perturbation due to the 2011 Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident. Another observation is that sporadic high 239,240Pu activity concentrations occurred in the east Japan Basin, ranging from 1 to 39 mBq m-3. The spatial distribution of 239,240Pu activity concentrations in surface waters revealed that high 239,240Pu levels (>20 mBq m-3) occurred in 1994 in the northern SOJ, which was considered to be due to winter convection. To elucidate factors controlling the temporal variability of surface 239,240Pu levels in the SOJ, a relationship between surface 239,240Pu activity concentrations and vertical diffusion coefficients was examined. The results revealed that this relationship could be classified into two groups: one group did not show a change with increasing diffusion coefficient, while the other group showed a positive correlation. The vertical 239,240Pu distribution in SOJ waters suggests that the high surface 239,240Pu levels occurred due to the upwelling of cyclonic eddy. The rapid recycling of deeper plutonium occurred in the SOJ due to deep winter convection and upwelling associated with cyclonic eddy. The plutonium levels in the SOJ have been found to be sensitive to climate changes. Warming of the SOJ may cause a reduction of winter convection and eddy activity as a result of increasing sea surface temperature. This leads to a decline of recirculation of plutonium and other bioavailable elements from Japan Sea Proper Water (JSPW) to surface water layers. Plutonium would be, therefore, an important indicator of biogeochemical processes in the marine environment, helping to assess climate change impacts on marine ecological systems.

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From early April 2020, wildfires raged in the highly contaminated areas around the Chernobyl nuclear power plant (CNPP), Ukraine. For about 4 weeks, the fires spread around and into the Chernobyl exclusion zone (CEZ) and came within a few kilometers of both the CNPP and radioactive waste storage facilities. Wildfires occurred on several occasions throughout the month of April. They were extinguished, but weather conditions and the spread of fires by airborne embers and smoldering fires led to new fires starting at different locations of the CEZ. The forest fires were only completely under control at the beginning of May, thanks to the tireless and incessant work of the firefighters and a period of sustained precipitation. In total, 0.7-1.2 TBq 137Cs were released into the atmosphere. Smoke plumes partly spread south and west and contributed to the detection of airborne 137Cs over the Ukrainian territory and as far away as Western Europe. The increase in airborne 137Cs ranged from several hundred µBq·m-3 in northern Ukraine to trace levels of a few µBq·m-3 or even within the usual background level in other European countries. Dispersion modeling determined the plume arrival time and was helpful in the assessment of the possible increase in airborne 137Cs concentrations in Europe. Detections of airborne 90Sr (emission estimate 345-612 GBq) and Pu (up to 75 GBq, mostly 241Pu) were reported from the CEZ. Americium-241 represented only 1.4% of the total source term corresponding to the studied anthropogenic radionuclides but would have contributed up to 80% of the inhalation dose.

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In order to study radiocarbon levels at a clean air location in Slovakia with no significant local anthropogenic effects, we took tree ring samples from a tree in the vicinity of Jasná recreational area in the Low Tatras region in the central part of Slovakia. There are no significant local fossil fuel emission sources, so these samples represent a regional clean air background important for 14C studies in Slovakia and Central Europe. The growth rings from the sampled tree (European spruce, Picea abies) cover the period from 1911 to 2016. The first part of the data (1911-1952) represents natural radiocarbon levels influenced by Suess effect. The following period exhibits an increase in radiocarbon levels due to atmospheric nuclear weapons tests (Δ14C maximum of 850‰ in 1964), and then a gradual decrease characterized by an exponential trend with time constant of 14.3 ± 0.5 years. The Δ14C data from Jasná was used as a reference for comparison with two previously reported modern tree ring data sets from Slovakia. This comparison showed that radiocarbon levels at both locations are lower than clean air reference values, indicating the influence of local fossil fuel emissions.

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The western North Pacific is one of the most studied oceanic basins due to its diverse structure and important role in connection with the adjacent reservoirs. Tritium (3H) and radiocarbon (14C) have been frequently exploited as oceanographic tracers due to their suitable properties; several extensive observation projects, such as GEOSECS, WOCE and WOMARS, used these two radionuclides to investigate different oceanographic processes, pathways, ocean currents and time scales of deep and bottom water formation. Here we evaluate temporal changes in 3H and 14C levels in seawater of the western North Pacific Ocean from 1993 to 2012. When compared to the background levels from 1993, the data from 2012 suggests significant impact of the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident on surface and vertical 3H seawater profiles, increasing its water column inventories in the southern part of the 149°E meridian by a factor of 2-7. On the other hand, 14C content in surface seawater has been steadily decreasing from 1993, with the accelerated rate from 2005, probably due to downwelling of bomb-produced radiocarbon and its transport along isopycnal layers. The influence of the Oyashio current on 14C levels in the northern part of the investigated transect and formation of its intrusion was also clearly visible in the collected datasets. Regarding bomb-produced radiocarbon, its water column inventories decreased or remained same from 2005 to 2012 at all stations, except the ones located in the coastal areas of the New Guinea island (3.5°S).

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Aerosols dispersed in the atmosphere represent important factors influencing not only the environment, but also human health. Carbonaceous aerosols are one of the main components of total atmospheric aerosols, and their sources are of great interest. Radiocarbon analysis provides an excellent way to determine the fraction of fossil and non-fossil aerosols in the atmosphere. Over the period of one year (June 2017-June 2018), we sampled atmospheric aerosols with size greater than 0.3 µm in Bratislava, Slovakia and used the exposed quartz filters for radiocarbon analysis of the elemental carbon (EC) aerosol fraction. The results show that on average the fossil fuel combustion is the dominant source of EC aerosol particles in Bratislava. In summer months, they represent more than half (65-80%) of the total EC aerosols. The relative amount of EC particles derived from biomass burning was 20-35% in summer, which increased to 40-55% in winter months. The dominance of fossil fraction is caused by high degree of industrialization and urbanization of the city. The increase of biomass fraction in winter is probably caused by domestic wood burning in areas surrounding the Bratislava city.

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Wine dating methods based on anthropogenic 14C and 137Cs, as well as on the cosmogenic 14C were studied with the aim to improve the accuracy and precision of the dating results. While the 14C dating method has proved to be useful for dating young and old wines, the 137Cs has been effective for dating of wines originating around the 137Cs bomb-peak observed in 1963. A new method was developed for simultaneous 14C and 137Cs dating of wines, which helped to distinguish wines originating before or after the bomb peak. The δ13C values also helped to solve the 14C age ambiguity in dating of wines around the 14C bomb peak. While the 14C dating method is always destructive one, the 137Cs method may use a radiochemical separation of cesium from wine samples when better precision of results is required, but it can be also a nondestructive one with direct gamma-spectrometry of wine samples, especially those that are very rare.

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Vertical distributions of 90Sr and 137Cs in Sea of Japan/East Sea (SOJ/ES) water in the period of 1977-2010 exhibited a typical diffusion shape with surface/subsurface maxima and decreasing values with increasing depth. Apparent vertical diffusion coefficients (AVDCs) and apparent initial surface fluxes (AIFs) of 90Sr and 137Cs, which were estimated using a curve-fitting method from a vertical diffusion model, showed temporal and spatial variability. A diffusion depth introduced for understanding of vertical movements of 90Sr and 137Cs in the SOJ/ES well correlated with corresponding AIFs, suggesting that spatial variations of the 90Sr and 137Cs inventories have been governed by oceanic conditions such as changes in AVDCs, which may be related with eddy field, characterizing the SOJ/ES. The temporal changes of the AVDCs suggest that the production of eddies increased during the 2000s comparing with that in the 1990s. These observations represent the first applications of radionuclides as tracers in production of oceanic eddies.

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Recently environmental radionuclide signals were observed in the atmosphere which could be associated with undeclared nuclear activities, not directly connected with development of nuclear weapons. Large-scale contamination of European air with Ru-106 observed in 2017 may represent such an accident, which was probably associated with the Mayak nuclear fuel reprocessing facility in the Chelyabinsk region of Russia. A recently announced nuclear accident at Nyonoska in the Archangelsk region may represent an undeclared nuclear activity associated with the development of a nuclear jet engine which could be based on radionuclide energy generator or a small nuclear reactor. It is concluded that environmental radioactivity impacts associated with recent nuclear activities create new challenges for fast and reliable national and international monitoring systems which would require development of new monitoring strategies.

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90Sr and 137Cs activity concentrations in surface waters of the Sea of Japan (SOJ) decreased during the period of 1993-2010 with effective half-lives of 18 and 15 y, respectively. The longer effective half-life of 90Sr in the SOJ may suggest a surplus of 90Sr to SOJ surface waters, however, no clear evidence of possible 90Sr source has been found. After the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, temporal variations of 137Cs in the surface water of the SOJ have changed, while 90Sr variations followed the pre-accident trends. The 90Sr/137Cs ratios reveal that increases of 137Cs due to the FDNPP accident continued in surface waters of the SOJ until 2016.

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Recent developments in radiometric and mass spectrometry technologies have been associated in the radiometric sector mainly with underground operations of large volume Ge detectors, while the mass-spectrometry sector, represented mainly by accelerator mass spectrometry and inductively coupled plasma mass spectrometry has become the most sensitive technique for ultra-low-level analyses of long-lived radionuclides. These new developments have had great impact on investigations of rare nuclear processes and applications of radionuclides in environmental, life and space sciences. New scientific investigations have been carried out therefore which have not been possible before either because of lack of sensitivity or required large sample size.

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Impact of the Fukushima Dai-ichi Nuclear Power Plant (FNPP1) accident on tritium (3H) and radiocarbon (14C) levels in the water column of the western North Pacific Ocean in winter 2012 is evaluated and compared with radiocesium (134,137Cs) data collected for the same region. Tritium concentrations in surface seawater, varying between 0.4 and 2.0 TU (47.2-236 Bq m-3), follow the Fukushima radiocesium trend, however, some differences in the vertical profiles were observed, namely in depths of 50-400 m. No correlation was visible in the case of 14C, whose surface Δ14C levels raised from negative values (about -40‰) in the northern part of transect, to positive values (∼68‰) near the equator. Homogenously mixed 14C levels in the subsurface layers were observed at all stations. Sixteen surface (from 30 in total) and 6 water profile (from 7) stations were affected by the Fukushima tritium. Surface and vertical profile data together with the calculated water column inventories indicate that the total amount of the FNPP1-derived tritium deposited to the western North Pacific Ocean was 0.7 ±â€¯0.3 PBq. No clear impact of the Fukushima accident on 14C levels in the western North Pacific was observed.

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