Fallout 137 Cs in reservoir sediment.
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In order to compare the transfer factors of 137Cs deposited after the fallout from the Chernobyl accident with 137Cs from nuclear weapons testing, soil and vegetation samples have been collected from a semi-natural ecosystem in western Norway. For the 137Cs from Chernobyl, 85% is found in the upper 5 cm of soil, whereas most of the nuclear weapons test 137Cs is found between 3 and 12 cm in the soil profile. The transfer factors from soil to vegetation are calculated to be 0.41 +/- 0.07 m2 kg-1 for the nuclear weapons test 137Cs and 0.40 +/- 0.22 m2 kg-1 for Chernobyl 137Cs. Hence, the results show no significant difference between the two fallouts. The effective ecological half-life of 137Cs for this ecosystem is estimated to be between 10 and 20 years. Wash-out and binding effects seem to be of minor importance for the uptake.
The vertical distribution of weapons testing fallout 237Np has been determined in an undisturbed grassland soil (Alfisol). By using a compartmental model for multi-layered soils, the mean residence half-times of 237Np in each soil layer were calculated and compared with results on weapons fallout 239 + 240Pu, 241Am and 137Cs in the same soil. The results show that the mobility of 237Np was in most soil horizons either equal or slightly enhanced as compared to that of Pu, Am, and radiocesium.
In three soils typical for Northern Germany including Eutric Cambisol, Orthic Podsol and Eutric Histosol (Food and Agriculture Organization nomenclature), distributions of 90Sr, 134Cs, 137Cs and 239Pu + 240Pu in the soil profiles were determined. Sampling was performed more than 3 years after deposition of Chernobyl fallout nuclides. Migration rates calculated with a compartmental model showed no significant differences between Cs originating from either atomic weapons or Chernobyl fallout. This result indicates that Chernobyl Cs may have reached sorption equilibrium with the soil matrix 3 years after the accident. Both the compartmental model and the dispersion equation reproduce distributions of most of the activities, but fail to reproduce some (minor) activity fractions that show increased mobility.
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To study the levels and distributions of radionuclides released in the Chernobyl accident, we sampled surface peat from 62 sites in Southern and Central Finland and measured 131I, 134Cs, 137Cs, 132Te, 140Ba, 103Ru, 90Sr, 141Ce, and 95Zr. The distribution of fallout activities was highly uneven, depending on movement of the contaminated air mass and rainfall distribution during the critical days. The highest values observed were 420 kBq m-2 of 131I and 70 kBq m-2 of 137Cs. The nuclide ratios showed wide and partly unexpected variations. The high-boiling-point, or nonvolatile, elements Ce and Zr were spread mostly on a 200-km-wide zone extending across Finland from southwest to northeast. The more volatile elements, I, Ce, and Te, showed quite a different, more widespread, fallout distribution, while an intermediate behavior was observed for Ba, Ru, and possibly Sr. These results can be explained by assuming that pulverized nuclear fuel material released in the reactor explosion on 26 April reached Finland via Poland and the Baltic Sea and traversed the country along the above-mentioned narrow zone, while volatile material, evaporated in the reactor fire from 26 April to 5 May, arrived in several waves and was consequently more widely and evenly spread. From their elemental melting and boiling points, Ru and Mo would appear to belong to the nonvolatile group and Sr to the volatile. Yet, their actual behaviors were opposite; Ru in particular was found in the nonvolatile as well as the volatile fallout, possibly because Ru activities were present in the fuel partly in the metallic state and partly as volatile oxides.
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