Precipitation scavenging of 7Be and 137Cs radionuclides in air

Atmospheric depositional fluxes of the naturally occurring 7Be of cosmogenic origin and 137Cs from fallout of the Chernobyl accident were measured over a 6-year period (January 1987-December 1992) at Thessaloniki, Greece (40 degrees 38'N, 22 degrees 58'E). Total precipitation accumulation during 1987-1992 varied between 33.7 cm and 65.2 cm, reflecting a relatively dry (precipitation-free) climate. The activity concentrations of 7Be and 137Cs in rainwater depended on the precipitation rate, being higher for low precipitation rates and lesser for high precipitation rates. 137Cs was removed by rain and snow more efficiently than 7Be. Snowfall was more efficient than rainfall in removing the radionuclides from the atmosphere. The annual bulk depositional fluxes of 7Be varied between 477 and 1133 Bq m(-2) y(-1) and this variability was attributed to the amount of precipitation and the variations of the atmospheric concentrations of 7Be. The annual bulk depositional fluxes of 137Cs showed a significant decrease over time from 1987 to 1992, resulting in a removal half-life of 1.33 years. The presence of 137Cs in air, and therefore in rainwater and snow, long after the Chernobyl accident (26 April 1986) was mainly due to the resuspension process. The normalized depositional fluxes of both radionuclides showed maximal values during the spring season where the maximum amount of precipitation occurred. The relatively high positive correlation between 7Be and 137Cs normalized depositional fluxes indicates that the scavenging process of local precipitation controlled the fluxes of both radionuclides. The dry depositional flux of 7Be was less than 9.37% of total (wet and dry) depositional flux. The fraction of dry-to-total depositional flux of 137Cs was much higher than that of 7Be, due to the resuspended soil.     

Temporal changes of 7Be, 137Cs and 210Pb activity concentrations in surface air at Monaco and their correlation with meteorological parameters

Results of analysis of ⁷Be, ¹³⁷Cs and ²¹⁰Pb on aerosol filters carried out from 1998 to 2010 in Monaco show that a weak correlation between activity concentrations of these radionuclides in the atmosphere and meteorological parameters has been found for ⁷Be and temperature (r = 0.50), ²¹⁰Pb and temperature and humidity (r = 0.43 and 0.41, respectively), and ¹³⁷Cs and precipitation (r = 0.51). The minimum and maximum ⁷Be activity concentrations were observed during 2000 and 2009, corresponding with the maximum and minimum solar activity, respectively. The maximum ¹³⁷Cs activity concentration found in May-June 1998 was due to the accident at Algeciras in Spain. The deposition velocities of ⁷Be, ¹³⁷Cs and ²¹⁰Pb depended on the precipitation rate, and attained maximum values during dry seasons. The investigated radionuclides may be used as atmospheric tracers, especially in long-term periods.     

137Cs distribution among annual rings of different tree species contaminated after the Chernobyl accident

The distributions of 137Cs among annual rings of Pinus sylvestris and Betula pendula at four experimental sites located in the most contaminated areas in the Russian territory after the Chernobyl accident in 1986 were studied. Trees of different ages were sampled from four forest sites with different tree compositions and soil properties. The data analysis shows that 137Cs is very mobile in wood and the 1986 rings do not show the highest contamination. The difference between pine and birch in the pattern of radial 137Cs distribution can be satisfactorily explained by the difference in radial ray composition. 137Cs radial distribution in the wood can be described as the sum of two exponential functions for both species. The function parameters are height, age and species dependent. The distribution of 137Cs in birch wood reveals much more pronounced dependence on site characteristics and/or the age of trees than pines. The data obtained can be used to assess 137Cs content in wood.     

Radioactivity in surface air and precipitation in Japan after the Chernobyl accident

Radioactive plumes from the Chernobyl reactor accident first passed over Japan on 3 May 1986. Measurements of ¹⁰³Ru, ¹³¹I and ¹³⁷Cs in rainfall and airborne dust collected at Chiba near Tokyo show that, in fact, at least two or more kinds of plume arrived during May. Their altitudes were calculated to be about 1500 m in early May and 6300 m in late May.Radionuclides detected in 33 precipitation samples collected by the network of prefectural radiation monitoring stations from 1 to 22 May were ⁷Be, ⁸⁹Sr, ⁹⁵Sr, ⁹⁵Zr, ⁹⁵Nb, ¹⁰³Ru, ¹⁰⁶Ru, ^110mAg, ¹²⁵Sb, ^129mTe, ¹³¹I, ¹³²Te, ¹³²I, ¹³⁴Cs, ¹³⁶Cs, ¹³⁷Cs, ¹⁴⁰Ba, ¹⁴⁰La, ¹⁴¹Ce and ¹⁴⁴Ce, the measurements being made using germanium detectors and low-background GM counters after radiochemical separation. The radiation was characterized by higher levels of the volatile nuclides, such as ¹⁰³Ru (in the form of RuO₂), ¹³²Te, ¹³¹I and ¹³⁷Cs, than fallout levels in nuclear weapons testing, and by activity ratios of 0·48 and 14 for, respectively, ¹³⁴Cs/¹³⁷Cs and ⁸⁹Sr/⁹⁰Sr, as on 26 April. The fallout activity was higher in northwestern Japan, the average depositions of ⁹⁰Sr and ¹³⁷Cs in Japan from 1 May (or 30 April) to 22 May being 1·4 Bq m⁻² and 95 Bq m⁻², inventories which are 14 and 550 times higher than the pre-Chernobyl values.     

Vertical migration studies of 137Cs from nuclear weapons fallout and the Chernobyl accident

The vertical migration of (137)Cs originating from nuclear weapons fallout (NWF) and the Chernobyl accident has been studied at 33 sampling sites in western Sweden. An attempt to describe the present depth distribution with a solution to the convection-diffusion equation (CDE) with a pulse-like fallout event as the initial condition was made. A sum of two CDEs describing the NWF and Chernobyl debris was fitted to the actual depth profiles measured by soil sampling. The fitted depth profiles were used to correct in situ measurements for the actual depth distribution, showing good agreement with the accumulated activities in soil samples. As expected, the vertical migration was very slow and most caesium was still present in the upper soil layers. The ranges of the apparent convection velocity, v, and apparent diffusion coefficient, D, were between 0 and 0.35 cm/year and 0.06 and 2.63 cm(2)/year, respectively.     

Simulation of 137Cs Migration over the Soil–Plant System of Peat Soils Contaminated after the Chernobyl Accident

A mathematical model was constructed to simulate the processes of ¹³⁷Cs migration in peat soils and its uptake by vegetation. Model parameters were assessed and the pattern of ¹³⁷Cs distribution over soil profile was predicted in case of peat soils, which are typical of the Russian regions contaminated after the Chernobyl accident. The ecological half-life of ¹³⁷Cs in the plant-root soil zone was calculated, and a long-term prognosis of the radionuclide uptake by plants was made.     

Soil-dependent uptake of 137Cs by mushrooms: experimental study in the Chernobyl accident areas

The influence of agrochemical properties of forest soils and growth conditions on 137Cs aggregated transfer factors from soil to different species of forest mushrooms have been analysed. Statistically significant correlations between 137Cs soil to mushroom aggregated transfer factors and agrochemical soil properties have been revealed. The experimental data show that 137Cs aggregated transfer factors depend on the mushroom's trophic group, biological family, genus and species. They also strongly depend on forest soil properties and their values can be estimated with the use of multiple regression equations constructed from agrochemical soil parameters which most closely correlate with the 137Cs transfer parameters for particular mushroom groups.     

Reconstruction of 137Cs signal in Cuba using 7Be as tracer of vertical transport processes in the atmosphere

Levels of 137Cs and 7Be in aerosols have been measured in the region of Cienfuegos (Cuba) during the period 1994-1998. 137Cs showed the same seasonal trend as 7Be and the monthly regimes of precipitation seemed to be responsible for the observed pattern. The 137Cs/7Be ratio obtained in Cienfuegos and Miami (FL) in this period was used to calibrate the long-term database of 137Cs concentrations recorded in Miami (250 km from Cienfuegos). The database was then employed to reconstruct the 137Cs monthly concentrations in Cienfuegos since 1957.     

137Cs concentration in meat of wild boars (Sus scrofa) in Croatia a decade and half after the Chernobyl accident

Gamma-spectrometric measurements of 137Cs activities in meat of wild boars collected in Croatia at several locations with different levels of 137Cs contamination are presented. Samples were collected during the period between 2000 and 2002, about 15 years after the Chernobyl accident. 137Cs concentrations ranged over three orders of magnitude: 0.4-611.5 Bq kg(-1). On the basis of these results, 137Cs concentrations at researched areas could be categorized into three groups: (i) the area of Slavonski Brod, Lipik and Slunj with 137Cs concentrations in meat of only a few Bq kg(-1); (ii) the area of Vrbovsko and Sirac with 137Cs concentrations of a few tens of Bq kg(-1); and (iii) the Fuzine area with 137Cs values in wild boar meat of a few hundreds of Bq kg(-1). In areas with approximately equal contamination level, 137Cs concentrations in wild boar meat varied over two orders of magnitude. This fact suggests that the main reason for high 137Cs values in wild boar meat could be due to food consumed by wild boars, and only secondarily in contamination level of area where they live. Intensive mushroom consumption during autumn months could be one of the factors responsible for high 137Cs values in wild boar meat. An average dose arising from 137Cs due to ingestion of wild boar meat in Croatia is below radiological health concern except in the area of Fuzine, and only in cases of high annual wild boar meat intake, probably by hunters or members of their families.     

Consequences of the Chernobyl reactor accident on the 137Cs internal dose to the Japanese population

The consequences of the Chernobyl reactor accident on the Japanese population are assessed here, for the one-year period from May 1986, in terms of the internal dose due to ¹³⁷Cs. The calculations are made via an approach which combines whole body counting with analysis of food intake data. First, the dose from ¹³⁷Cs is assessed, for a group of healthy adult males, on the basis of their observed body burdens of ¹³⁷Cs determined by whole body counting. The annual individual dose estimate thus obtained is 1·5 μSv, which is 6–15% and 3·7% respectively of the doses determined by whole body counting in UK and the Federal Republic of Germany. The temporal change in the average body burden is successfully explained here by a single-compartment model. Secondly, this latter model is used, along with the daily ¹³⁷Cs intake data for each district in Japan, to calculate the dose for the whole of Japan. Appropriate values were chosen for the relevant biological parameters for each age and sex group. The estimates of the population dose and the average individual dose thus obtained are 148 man Sv, for the population of 120 million, and 1·24 μSv, respectively. Although comparatively small, these values nonetheless also include the residual contribution from past nuclear weapon tests. The average annual individual dose of 1·24 μSv corresponds to 0·7% of the dose from natural ⁴⁰K in the body. Although whole body counting indicates that ¹³⁷Cs burdens were still increasing as of May 1987, it is concluded that, in terms of radiocaesium, the effect of the Chernobyl reactor accident on Japan was negligible.     

Describing the annual cyclic behaviour of 7Be concentrations in surface air in Oceania

Surface air concentrations of (7)Be at a number of stations in Oceania show a distinct annual cycle. We apply a sinusoidal model to describe this cycle. The results show that peak (7)Be concentrations in surface air occur during early spring at tropical latitudes and during mid-to-late summer at middle latitudes. Comparison with available (90)Sr surface air data for the southern hemisphere indicates that stratosphere-to-troposphere exchange is an active atmospheric process controlling the (7)Be annual cycle throughout the Oceania region. Vertical transport of air within the troposphere also seems to influence the observed annual cycle. Seasonality in rainfall is not thought to control the annual cyclic behaviour of (7)Be in surface air.     

Distribution of fallout radionuclides (7Be, 137Cs, 210Pb and 239,240Pu) in soils of Taiwan

Depth profiles and cumulative deposition of four fallout radionuclides (7Be, 137Cs, 210Pb and 239,240Pu) were determined in presumably undisturbed soils in Taiwan. Inventories of these radionuclides in different areas correlate significantly with each other (except 7Be) and with mean annual rainfall, providing a necessary condition for the development of soil erosion studies in Taiwan. However, the data show very large spatial variability between and within landscape units, reflecting the steep topographic and meteorological gradients in the island. Thus, the application of fallout radionuclides to study soil conservation in Taiwan is expected to be a demanding task; it will call for dense sampling even at undisturbed reference sites.     

Model testing using data on 137Cs from Chernobyl fallout in the Iput River catchment area of Russia

Data collected for 10 years following the Chernobyl accident in 1986 have provided a unique opportunity to test the reliability of computer models for contamination of terrestrial and aquatic environments. The Iput River scenario was used by the Dose Reconstruction Working Group of the BIOMASS (Biosphere Modelling and Assessment Methods) programme. The test area was one of the most highly contaminated areas in Russia following the accident, with an average contamination density of 137Cs of 800,000 Bq m-2 and localized contamination up to 1,500,000 Bq m-2, and a variety of countermeasures that were implemented in the test area had to be considered in the modelling exercise. Difficulties encountered during the exercise included averaging of data to account for uneven contamination of the test area, simulating the downward migration and changes in bioavailability of 137Cs in soil, and modelling the effectiveness of countermeasures. The accuracy of model predictions is dependent at least in part on the experience and judgment of the participant in interpretation of input information, selection of parameter values, and treatment of uncertainties.     

Vertical distributions of 210Pb excess, 7Be and 137Cs in selected grass covered soils in Southeast Queensland, Australia

Net accumulated areal activity densities and profiles of (210)Pb(ex), (7)Be and (137)Cs in the surface 10 cm of the soil are reported for eight sites in Southeast Queensland, Australia. Areal activity densities of (210)Pb(ex) and (7)Be varied from 1,080 to 4,100 Bqm(-2) and from 176 to 778 Bqm(-2), respectively. A significant (p < 0.001) portion of the variance (R(2) > 0.99) in their vertical distributions was explained by depth in the profile using an exponential function. Around 85% of accumulated (210)Pb(ex) was present in the surface 10 cm of the soil. Beryllium-7 was mainly confined to the grass and surface 2 cm of the soil. Average penetration half-depths of 3.6 +/- 0.2 and 0.3 +/- 0.1cm were determined for (210)Pb(ex) and (7)Be, respectively. Areal activity densities of global fallout (137)Cs varied from 10 to 361 Bqm(-2). Its signal was well mixed within the surface 10 cm. Comparison of the measured (137)Cs values to the estimated input value for the region ( approximately 490 Bqm(-2)) and profiling of a 1m deep soil core suggests a vertical migration of (137)Cs over the past decades. The paleo-radon activity flux determined from the (210)Pb(ex) areal activity density (5.1 +/- 0.9 mBqm(-2) s(-1)) was not statistically different to that measured using activated charcoal cups (5.5 +/- 0.4 mBqm(-2) s(-1)), tending to suggest that Southeast Queensland is neither a net source nor a net sink of (210)Pb-bearing aerosols.     

Plutonium, 137Cs and 90Sr in selected invertebrates from some areas around Chernobyl nuclear power plant

Results are presented for ¹³⁷Cs, ⁹⁰Sr and plutonium activity concentrations in more than 20 samples of terrestrial invertebrates, including species of beetles, ants, spiders and millipedes, collected in the highly contaminated area of the Chernobyl exclusion zone. The majority of samples were collected in Belarus, with some also collected in the Ukraine. Three other samples were collected in an area of lower contamination. Results show that seven samples exceed an activity concentration of 100 kBq/kg (ash weight - a.w.) for ¹³⁷Cs. The maximum activity concentration for this isotope was 1.52 ± 0.08 MBq/kg (a.w.) determined in ants (Formica cynerea). Seven results for ⁹⁰Sr exceeded 100 kBq/kg (a.w.), mostly for millipedes. Relatively high plutonium activity concentrations were found in some ants and earth-boring dung beetles. Analyses of activity ratios showed differences in transfer of radionuclides between species. To reveal the correlation structure of the multivariate data set, the Partial Least-Squares method (PLS) was used. Results of the PLS model suggest that high radiocesium activity concentrations in animal bodies can be expected mainly for relatively small creatures living on the litter surface. In contrast, high strontium activity concentrations can be expected for creatures which conduct their lives within litter, having mixed trophic habits and a moderate lifespan. No clear conclusions could be made for plutonium.     

Global and local cancer risks after the Fukushima Nuclear Power Plant accident as seen from Chernobyl: A modeling study for radiocaesium (134Cs & 137Cs)

The accident at the Fukushima Daiichi Nuclear Power Plant (NPP) in Japan resulted in the release of a large number of fission products that were transported worldwide. We study the effects of two of the most dangerous radionuclides emitted, ¹³⁷Cs (half-life: 30.2 years) and ¹³⁴Cs (half-life: 2.06 years), which were transported across the world constituting the global fallout (together with iodine isotopes and noble gasses) after nuclear releases. The main purpose is to provide preliminary cancer risk estimates after the Fukushima NPP accident, in terms of excess lifetime incident and death risks, prior to epidemiology, and compare them with those occurred after the Chernobyl accident. Moreover, cancer risks are presented for the local population in the form of high-resolution risk maps for 3 population classes and for both sexes. The atmospheric transport model LMDZORINCA was used to simulate the global dispersion of radiocaesium after the accident. Air and ground activity concentrations have been incorporated with monitoring data as input to the LNT-model (Linear Non-Threshold) frequently used in risk assessments of all solid cancers. Cancer risks were estimated to be small for the global population in regions outside Japan. Women are more sensitive to radiation than men, although the largest risks were recorded for infants; the risk is not depended on the sex at the age-at-exposure. Radiation risks from Fukushima were more enhanced near the plant, while the evacuation measures were crucial for its reduction. According to our estimations, 730–1700 excess cancer incidents are expected of which around 65% may be fatal, which are very close to what has been already published (see references therein). Finally, we applied the same calculations using the DDREF (Dose and Dose Rate Effectiveness Factor), which is recommended by the ICRP, UNSCEAR and EPA as an alternative reduction factor instead of using a threshold value (which is still unknown). Excess lifetime cancer incidents were estimated to be between 360 and 850, whereas 220–520 of them will be fatal. Nevertheless, these numbers are expected to be even smaller, as the response of the Japanese official authorities to the accident was rapid. The projected cancer incidents are much lower than the casualties occurred from the earthquake itself (> 20,000) and also smaller than the accident of Chernobyl.     

(137)Cs concentrations in Atlantic and western Antarctic surface waters: results of the 7th Ukrainian Antarctic Expedition, 2002

The latitudinal distribution of (137)Cs in the Atlantic--western Antarctic surface waters was studied during the 7th Ukrainian Antarctic Expedition in January--May 2002. The (137)Cs concentrations have also been measured in the upper ice of the coastal glacier Woozle Hill located near the Ukrainian Antarctic station "Akademik Vernadsky" (western Antarctica, 65 degrees 15' S-64 degrees 16' W). Comparison of these data with results of previous same-route expeditions SWEDARP (Swedish Antarctic Research Expedition, 1988/1989) and the French R/V "Jeanne d'Arc" (1992/1993), has shown practically parallel changes of (137)Cs surface concentrations between 40 degrees N and 20 degrees S, pointing to decrease of (137)Cs radioactivity at these latitudes with an apparent half-life of 10--15 years (12.5+/-2.1 years on average). This suggests that decrease of (137)Cs surface concentration within this latitude band is controlled, besides the radioactive decay of (137)Cs (half-life=30 years), by vertical mixing of the upper water masses. South of 20 degrees S, the (137)Cs concentrations in surface water have decreased more rapidly because of the influence of the less contaminated Antarctic waters. At 50--60 degrees S and near the Antarctic coast, the (137)Cs activity in 2002 was similar to those measured during the SWEDARP and "Jeanne d'Arc" expeditions, suggesting an additional input of (137)Cs to these waters from the melted ice from the adjacent glaciers.     

Present background levels of surface 137Cs and (239,240)Pu concentrations in the Pacific

The present levels of anthropogenic radionuclides, 137Cs and (239,240)Pu, in surface waters of the Pacific are estimated using the HAM database, which is a comprehensive data set of 137Cs, (239,240)Pu and other anthropogenic radionuclides. The time-series data of surface 137Cs and (239,240)Pu suggests that surface 137Cs and (239,240)Pu concentrations in the Pacific since 1971 decrease exponentially in each sea area, although the temporal changes of surface 137Cs and (239,240)Pu differed between sea areas of the Pacific. The calculated 137Cs concentrations in the Pacific surface waters in 2000 are homogeneous in the Pacific, comparing with that in the 1960s and 1970s, although they are still high in the North Pacific and low in the South Pacific. The biogeochemical and physical processes are significant factors to control present levels of surface (239,240)Pu concentrations, which are high in the Subarctic and equatorial Pacific and low in the mid-latitude region of the eastern North Pacific.     

Distribution of 137Cs in the Tree Layer of Forest Ecosystems in the Zone of the Accident at the Chernobyl Nuclear Power Plant

Trends in ¹³⁷Cs distribution over the parts of coniferous (Pinus sylvestrisL.) and deciduous (Betula pendula Rocht.) trees are described. The trees have been selected in the stationary experimental plots located in southwestern Bryansk oblast, Russian Federation. The distribution of ¹³⁷Cs in the wood along the trunk height is shown to be nonuniform. The effects of ¹³⁷Cs content in the xylem sap on the accumulation of this radionuclide in the leaves and needles are assessed. The factors controlling ¹³⁷Cs accumulation in the components of woody plants are revealed, and their significance is estimated.