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Yablokov et al.: Atmospheric, Water, and Soil Contamination 229TABLE 8.7. Rainfall and Surface Water Radionuclide Concentrations in Several Countries, 1986–1987MaximumRadionuclide concentration Location Date ReferenceCs-137 5,300 Bq/m 3∗ Finland 1986 Saxen and Aaltonen, 1987325 mBq/liter Canada, Ontario May 1986 Joshi, 1988700 Bq/liter France, Paris Apr. 29–30, 1986 Thomas and Martin, 1986Sr-89 11,000 Bq/m 3 Finland 1986 Saxen and Aaltonen, 1987Te-132 7,400 Bq/liter France, Paris Apr. 29–30, 1986 Thomas and Martin, 1986∗ About 1,000 times higher than the precatastrophe concentration, and up to 80 times higher than the highest valuesafter the nuclear weapons test period in the 1960s.(2.7 kBq/liter for I-131 and 2.3 kBq/liter eachfor Te-132 and I-132). The total activity precipitatedper square kilometer in this periodwas about 55 GBq (Beentjes and Duijsings,1987).6. POLAND. Average values <strong>of</strong> Pu-239 + Pu-240 in the Polish economic zone <strong>of</strong> the BalticSea ranged from 30 to 98 Bq/m 2 in three samplinglocations. The highest concentration <strong>of</strong>Pu in sediment probably came from the VistulaRiver, which delivered 192 MBq <strong>of</strong> Chernobyl’sPu-239 + Pu-240 to the Baltic Sea in1989 (Skwarzec and Bojanowski, 1992). Thetotal Cs-137 loading <strong>of</strong> Lake Sniardwy was estimatedto average 6,100 Bq/m 2 (Robbins andJasinski, 1995).7. SWEDEN. The annual mean concentration<strong>of</strong> Cs-137 (in Bq/kg) in surface water nearGotland Island from 1984 to 2004 is shown inFigure 8.2.TABLE 8.8. Composition and Activity <strong>of</strong> the ChernobylRadioactive Fallout in Thessaloniki, Greece,(Total Wet Deposition, Bq/m 2 ), May 5–6, 1986 (Papastefanouet al., 1988)RadionuclideMaximum concentrationI-131 117,278Te-132 70,700I-132 64,686Ru-103 48,256Ba-140 35,580Cs-137 23,900La-140 15,470Cs-134 12,2768. TYRRHENIAN SEA. Concentration <strong>of</strong> Cs-137 in surface water <strong>of</strong> the Tyrrhenian Sea rosesignificantly immediately after the catastrophe(Figure 8.3).8.3. Chernobyl’s Contamination<strong>of</strong> the Soil MantleThe soil mantle will accumulate Chernobyl’sradionuclides with long half-lives for centuries.As in the previous review, this material is onlya representative selection from the very largebody <strong>of</strong> existing data.8.3.1. Belarus, Ukraine, and Russia1. Radionuclides on sod-podzol and heavilypodzolized sandy clay soils move from thesurface to the bottom soil layer during thecourse <strong>of</strong> time, resulting in the concentration <strong>of</strong>radionuclides in the root zone. It is in thisway that soils with low surface contaminationtransfer radioactivity to the vegetative (and edible)parts <strong>of</strong> plants (Borysevich and Poplyko,2002).2. Plowed and natural pastures located 50to 650 km from the Chernobyl site have levels<strong>of</strong> Cs-137 activity in the 1,000 to 25 kBq/m 2range in the upper soil layers (0–5 cm). Levels <strong>of</strong>contamination are higher in natural pastures ascompared with plowed pastures, with the Sr-90activity ranging from 1.4 to 40 kBq/m 2 (Salbuet al., 1994).

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