Formation of radioactivity enriched soils in mountain areas

A field study was carried out in the Mercantour Mountains at 2200 m altitude to investigate the processes of soil enrichment in atmospheric Chernobyl (137)Cs. Soils with high (137)Cs activities have been collected in the pasture areas with frequently measured (137)Cs activity values of the order of 7000 Bq m(-2). At some single spots (about 6% of the studied area), activity in soils reached 300000 Bq m(-2), which represents 44% of the (137)Cs of the total area. Data further showed that spatial distribution of Cs depends widely on its origin: Chernobyl Cs is mainly concentrated in "enriched" soils, whereas older Cs and (241)Am fallout from nuclear weapons tests (NWTs) and natural atmospheric (210)Pb in soils is less heterogeneously distributed.In order to elucidate the processes which have led to the enrichment in Chernobyl (137)Cs in the Alps in May of 1986, we have studied the repartition of atmospheric (7)Be isotope (half-life=53.3 d) in the pasture compartments (soil, litter, grass, and snow). Snow (7)Be data give evidence that fallout enrichment is related to snow accumulation (snow drift). The transfer of beryllium occurs rapidly to the grass and litter, where the strongest pollutant accumulations were measured. However, (7)Be transport to the soil required more than 8 months.     

南京地区7Be沉降特征

7Be是研究大气科学与地球化学的核元素之一,对研究短期过程的地表土壤颗粒迁移具有较大价值。为了解南京地区利用7Be进行土壤侵蚀示踪研究的合适时机,于2010年1月~2011年12月收集南京地区各月的7Be沉降样品,经实验室化学实验处理和γ谱仪测量,计算7Be沉降通量,并分析7Be大气沉降的季节性变化趋势。结果表明：南京地区平均7Be沉降量为1 62178 Bq/（m2·a）,沉降通量为066～1449 Bq/（m2·d）,平均沉降通量为444 Bq/（m2·d）;7Be沉降通量的季节变化呈现双峰型趋势,冬末春初和夏季是两个高值区;7Be沉降的а值冬春季较大,夏季最低;降雨量大小与沉降量存在明显的正相关     

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.     

Evaluation of 137Cs fallout from the Chernobyl accident in a forest soil and its impact on Alpine Lake sediments, Mercantour Massif, S.E. France

The Boréon area in the Mercantour Massif, S.E. France, was contaminated by radionuclides after the Chernobyl accident in the first days of May 1986. Sediments from a small mountain lake in this area were collected, as well as forest soils in its vicinity, in order to obtain 137Cs and 210Pb profiles. Calculated from the 210Pb inventory in a soil of a horizontal area, the flux is high in the area (0.06 Bqcm(-2)y(-1)) probably because of the great frequency of rain and uranium ores outcropping in the massif. The comparison of the 137Cs soil inventories and the unsupported 210Pb suggests that the 137Cs fallout due to the Chernobyl accident in the study site (Boréon) was at least 3.5 Bqcm(-2), more probably the double. The recent lake sediments still undergo a rather strong contamination by 137Cs and the sediment profiles show that the residence time of 137Cs in the catchment area is long. The study area is frequented by many inhabitants of the city of Nice and other cities at the Mediterranean coast during week-end and during summer and winter holidays. Thus the 137Cs external exposure impact was evaluated at 2 mSvy(-1) for 2002 in the most contaminated point.     

Coloured rain dust from Sahara Desert is still radioactive

A coloured rain event originating from the Sahara Desert occurred on April 9, 2000 at Thessaloniki, Northern Greece (40 degrees 38'N, 22 degrees 58'E). The radioactive nuclides that were determined in a coloured rain dust sample were 137Cs of Chernobyl origin, 7Be of cosmogenic origin and 40K of terrestrial origin. Cesium-137 still remained 14 years after the Chernobyl accident, reaching 26.6 Bq kg-1 in the coloured rain dust.     

210Pb and 137Cs as chronometers for salt marsh accretion in the Venice Lagoon - links to flooding frequency and climate change

Five salt marsh sediment cores from different parts of the Venice Lagoon were studied to determine their depositional history and its relationship with the environmental changes occurred during the past approximately 100 years. X-radiographs of the cores show no disturbance related to particle mixing. Accretion rates were calculated using a constant flux model applied to excess (210)Pb distributions in the cores. The record of (137)Cs fluxes to the sites, determined from (137)Cs profiles and the (210)Pb chronologies, shows inputs from the global fallout of (137)Cs in the late 1950s to early 1960s and the Chernobyl accident in 1986. Average accretion rates in the cores are comparable to the long-term average rate of mean sea level rise in the Venice Lagoon ( approximately 0.25 cm y(-1)) except for a core collected in a marsh presumably affected by inputs from the Dese River. Short-term variations in accretion rate are correlated with the cumulative frequency of flooding, as determined by records of Acqua Alta, in four of the five cores, suggesting that variations in the phenomena causing flooding (such as wind patterns, storm frequency and NAO) are short-term driving forces for variations in marsh accretion rate.     

The radiological impact of the Chernobyl debris compared with that from nuclear weapons fallout

Our basic knowledge of the radiological impact of fallout from nuclear accidents is based on the experience gained from the study of nuclear weapons fallout. Radioecologically, the most important radionuclides generated by the Chernobyl accident were ¹³⁷Cs, ¹³⁴Cs, ¹³¹I and, to a lesser degree, ⁹⁰Sr. These nuclides are well known from global fallout, although in different relative amounts to those observed in the Chernobyl debris. Another important difference between the fallout from Chernobyl and that from nuclear weapon tests is that their seasonal and geographical distributions were quite dissimilar. A number of examples show how these differences influenced transfer factors and thus population doses. Special emphasis is paid to the contamination of milk and cereal products.Furthermore, it is shown how the composition of the Chernobyl debris changed with distance from Chernobyl, due to the differences in volatility of the various radionuclides involved. Finally, the paper compares the dose equivalents received from unit releases (1 P Bq ¹³⁷Cs) of global fallout and of Chernobyl accident debris.     

Determining the Chernobyl impact on sediments of a pre-Alpine lake with a very comprehensive set of data

Man-made and natural radionuclides in Lake Wallersee were determined in the pre-Alpine environment at the northern slope of the Alps, which was heavily affected by the Chernobyl fallout in May 1986. The objective of this study was to get knowledge of location and quantity of man-made radionuclide input (especially (137)Cs) generated in the Chernobyl accident to lake sediments. Eleven sediment cores were sampled and activity depth profiles of (137)Cs and (210)Pb were determined with 5mm depth-resolution. The Chernobyl fallout produced an extreme (137)Cs peak in the sediment cores providing an excellent time marker. The chronological interpretation of deeper sediment layers was done by radiochemical analysis of (90)Sr and (239+240)Pu, which were released during atmospheric weapons' tests in the 1950s and 1960s. This allowed a complete chronological analysis of the sediment cores with a very compact set of data.     

Seasonal 7Be and 137Cs activities in surface air before and after the Chernobyl event

Seasonal fluctuations of cosmogenic (7)Be (T(1/2)=53.4 days) and anthropogenic (137)Cs (T(1/2)=30 years) activities in surface air (aerosols) have been extracted from a long data record (1972-2000) at high latitude (56 degrees N-68 degrees N, Sweden). Normalization to weekly average values was used to control long-term trends so that cyclical trends could be investigated. Enhanced (7)Be activity was observed in spring and summer seasons and likely relates to the seasonal thinning of the tropopause. Variations in the (137)Cs activity record seem to reflect how the isotope was injected in the atmosphere (stratospheric from bomb tests and tropospheric from the Chernobyl accident) and subsequent transport mechanisms. Accordingly, until 1986, the surface air (137)Cs activity was strongly related to nuclear weapons test fallout and exhibits temporal fluctuations resembling the (7)Be. Conversely, since 1986 the Chernobyl-produced (137)Cs dominates the long-term record that shows annual cycles that are strongly controlled by atmospheric boundary layer conditions. Additionally, short-term data within the post-Chernobyl period suggest subtle intrusion of air masses rich in (137)Cs that may occur throughout the year, and differences resulting from spatial occurrence at these latitudes. This is an important observation that may have to do with year-to-year variation and calls for caution when interpreting short-term data records.     

The marine impact of caesium-134 and -137 from the Chernobyl reactor accident

¹³⁴Cs and ¹³⁷Cs from the Chernobyl reactor accident were detected in UK shoreline seawater very quickly after activity from the accident reached this country. Concentrations were highest in areas adjacent to those where deposition over land was highest, but they declined quickly and did not reach radiologically significant levels in terms of public radiation exposure. Subsequently, the distribution in seawater was investigated further afield. Radiocaesium attributable to the Chernobyl accident was found to be widespread: it was readily distinguished from other sources by having a different ¹³⁷Cs:¹³⁴Cs ratio (about 2:1). Its presence was especially noticeable in northern UK waters rather than those to the south; much of the North Sea has been surveyed as well as the Norwegian Sea. Evidence of Chernobyl radiocaesium was found as far north as 70°N and in many of these areas, including the northern North Sea, it overshadowed the effect of BNFL (British Nuclear Fuels plc) Sellafield discharges, previously the main source of these radionuclides.     

Occurrence and behaviour of radionuclides in the Moselle River—Part I: Entry of natural and artificial radionuclides

Various sources contribute to the radioactive contamination of the Moselle River, among which the French NPP Cattenom with four units of 1300 M We represents the most important. Appropriate operational precautions were taken in order to monitor the nuclide transfer on different pathways under normal and accidental conditions and the effectiveness of these measures has been tested using natural (²¹⁴Pb/²¹⁴Bi, ⁷Be, ⁴⁰K) and artificial radionuclides. (³H, ⁵⁸Co, ⁶⁰Co, ¹³¹I, ¹³⁷Cs) as tracers. Measurements of suspended matter have revealed that the inputs of natural nuclides exceed the discharges of the NPP Cattenom. In 1992 the annual loads of ⁷Be and ⁴⁰K in suspended matter at Palzem amounted to 21 and 130 GBq year⁻¹, whereas the emission rates of ⁶⁰Co and ¹³⁷Cs were about 2.6 and 1.0 GBq year⁻¹. The total nuclide load of ¹³⁷Cs at Palzem reached 6.2 GBq year⁻¹, which is about six times the quantity emitted by the NPP Cattenom in the same year. This excess is due to the accident at Chernobyl and to a lesser extent to prior atmospheric weapons tests.     

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.     

Determination of radionuclide levels in rainwater using ion exchange resin and γ-spectrometry

The evaluation of radioactivity accidentally released into the atmosphere involves determining the radioactivity levels of rainwater samples. Rainwater scavenges atmospheric airborne radioactivity in such a way that surface contamination can be deduced from rainfall rate and rainwater radioactivity content. For this purpose, rainwater is usually collected in large surface collectors and then measured by γ-spectrometry after such treatments as evaporation or iron hydroxide precipitation. We found that collectors can be adapted to accept large surface (diameter 47 mm) cartridges containing a strongly acidic resin (Dowex AG 88) which is able to quantitatively extract radioactivity from rainwater, even during heavy rainfall. The resin can then be measured by γ-spectrometry. The detection limit is 0.1 Bq per sample of resin (80 g) for ¹³⁷Cs. Natural ⁷Be and ²¹⁰Pb can also be measured and the activity ratio of both radionuclides is comparable with those obtained through iron hydroxide precipitation and air filter measurements. Occasionally ²²Na has also been measured above the detection limit. A comparison between the evaporation method and the resin method demonstrated that 2/3 of ⁷Be can be lost during the evaporation process. The resin method is simple and highly efficient at extracting radioactivity. Because of these great advantages, we anticipate it could replace former rainwater determination methods. Moreover, it does not necessitate the transportation of large rainwater volumes to the laboratory.     

Accumulation of radionuclides from radioactive substrata by some micromycetes

Overgrowing (interaction) and dissolution of intact and milled hot particles by various micromycetes were studied under laboratory conditions. Hot particles used for the investigation originated from the Chernobyl accident release and atomic bomb testing sites. The micromycetes investigated were mitosporic fungi mainly isolated from the Chernobyl site and vicinity. Most of the fungal species and strains showed a tendency to grow towards the hot particle, overgrow it and dissolve it after prolonged contact. The accumulation (absorption and adsorption) of radionuclides from intact hot particles was generally more intensive for (152)Eu than for (137)Cs by a factor of about 2.6-134, while in experiments with milled samples the (152)Eu and (137)Cs accumulation was similar, except for some fungal species, which showed higher (152)Eu than (137)Cs sorption. It could be shown that the main factors influencing Cs and Eu accumulation in fungi are: fungal species and strains and the size and composition of the hot particle.     

Radioactivity in tobacco leaves

The radioactivity in tobacco leaves collected from 15 different regions of Greece before cigarette production was studied in order to find any association between the uptake of the naturally occurring radionuclides and the isotopes of cesium of Chernobyl origin. The activities of the isotopes of radium, 226Ra and 228Ra, in the tobacco leaves reflected their origin from the soil by root uptake rather than from fertilizers used in the tobacco cultivation. Lead-210 originated from the air and was deposited onto the tobacco leaves and trapped by the trichomes. Potassium-40 in the tobacco leaves was due to root uptake either from soil or from fertilizer. The isotopes of cesium, 137Cs and 134Cs, in the tobacco leaves were due to root uptake and not due to deposition onto the leaf foliage as they still remained in soil four years after the Chernobyl reactor accident but were absent from the atmosphere in rain washout (precipitation) and gravitational settling.     

A 10-year study of the 137Cs distribution in soil and a comparison of Cs soil inventory with precipitation-determined deposition

During a 10-year period, 1988-1998, surface soil samples have been collected at Blentarp in southern Sweden and analysed for 137Cs from the Chernobyl accident and from the nuclear weapons tests. The distance between the sampling plots on the different sampling occasions has been no more than 3 m. The results show that the depth distribution of 137Cs is very similar for each of the sampling occasions, indicating that the caesium migration at this site is very small. The total activity measured in the soil cores is in agreement with the calculated activity of 137Cs deposited at the site after nuclear weapons tests and the Chernobyl accident, based on air activity concentration and the amount of precipitation. The calculated deposition of 137Cs originating from the bomb tests amounts to 1.41 kBq m-2 for the period 1962-1986, which is in agreement with the activity of nuclear weapons fallout measured in the soil samples (1.60 kBq m-2 as a mean value of the first four years of sampling). The calculated activity of 137Cs of Chernobyl origin was 0.79 kBq m-2, which agrees well with the value of 0.79 kBq m-2 measured in the soil samples in 1988.     

Mesoscale modelling of radioactive contamination formation in Ukraine caused by the Chernobyl accident

This work is devoted to the reconstruction of time-dependent radioactive contamination fields in the territory of Ukraine in the initial period of the Chernobyl accident using the model of atmospheric transport LEDI (Lagrangian-Eulerian DIffusion model). The modelling results were compared with available 137Cs air and ground contamination measurement data. The 137Cs atmospheric transport over the territory of Ukraine was simulated during the first 12 days after the accident (from 26 April to 7 May 1986) using real aerological information and rain measurement network data. The detailed scenario of the release from the accidental unit of the Chernobyl nuclear plant has been built (including time-dependent radioactivity release intensity and time-varied height of the release). The calculations have enabled to explain the main features of spatial and temporal variations of radioactive contamination fields over the territory of Ukraine on the regional scale, including the formation of the major large-scale spots of radioactive contamination caused by dry and wet deposition.     

Evidence of the radioactive fallout in the center of Asia (Russia) following the Fukushima Nuclear Accident

It was recently reported that radioactive fallout due to the Fukushima Nuclear Accident was detected in environmental samples collected in the USA and Greece, which are very far away from Japan. In April-May 2011, fallout radionuclides (¹³⁴Cs, ¹³⁷Cs, ¹³¹I) released in the Fukushima Nuclear Accident were detected in environmental samples at the city of Krasnoyarsk (Russia), situated in the center of Asia. Similar maximum levels of ¹³¹I and ¹³⁷Cs/¹³⁴Cs and ¹³¹I/¹³⁷Cs ratios in water samples collected in Russia and Greece suggest the high-velocity movement of the radioactive contamination from the Fukushima Nuclear Accident and the global effects of this accident, similar to those caused by the Chernobyl accident.     

Radionuclides deposition over Antarctica

A detailed and comprehensive map of the distribution patterns for both natural and artificial radionuclides over Antarctica has been established. This work integrates the results of several decades of international programs focusing on the analysis of natural and artificial radionuclides in snow and ice cores from this polar region. The mean value (37+/-20 Bq m(-2)) of (241)Pu total deposition over 28 stations is determined from the gamma emissions of its daughter (241)Am, presenting a long half-life (432.7 yrs). Detailed profiles and distributions of (241)Pu in ice cores make it possible to clearly distinguish between the atmospheric thermonuclear tests of the fifties and sixties. Strong relationships are also found between radionuclide data ((137)Cs with respect to (241)Pu and (210)Pb with respect to (137)Cs), make it possible to estimate the total deposition or natural fluxes of these radionuclides. Total deposition of (137)Cs over Antarctica is estimated at 760 TBq, based on results from the 90-180 degrees East sector. Given the irregular distribution of sampling sites, more ice cores and snow samples must be analyzed in other sectors of Antarctica to check the validity of this figure.     

238Pu, 239,240Pu, 241Am, 90Sr and 137Cs in soils around nuclear research centre Rez, near Prague

Forty-four soil samples were taken around the nuclear research centre Rez, near Prague. The mean activity concentrations of 238Pu, 239,240Pu, 241Am, 90Sr and 137Cs in uncultivated soil were 0.010, 0.26, 0.12, 2.7 and 23 Bq.kg(-1), respectively. Contents of radionuclides in cultivated soil were lower and in forest soil higher than in uncultivated soil. The mean activity ratios of 238Pu/239,240Pu, 241Am/239,240Pu, 90Sr/239,240Pu and 239,240Pu/137Cs in uncultivated soil were 0.041, 0.47, 10.9 and 0.013, respectively. The mean activity ratios in cultivated and forest soils were close to the values given above. It follows from the results that the source of 239,240Pu, 90Sr and 137Cs in the studied area is deposition from atmospheric nuclear tests, in the case of 137Cs also deposition from Chernobyl accident. The contribution of the research centre effluents was not proved for these radionuclides. Increased activity ratio of 241Am/239,240Pu indicates the presence of 241Am in the soils studied emanating from sources other than nuclear tests. Uniform distribution of the 241Am/239,240Pu activity ratio around the nuclear research centre and the absence of an area with evidently higher activity ratio, including at sites lying in the main wind direction, suggest that the additional activity of 241Am does not originate from the nuclear research centre. The additional source might be the deposition following the Chernobyl accident.