PLUTONIUM RELEASED BY THE NAGASAKI A-BOMB - MOBILITY IN THE ENVIRONMENT
PLUTONIUM RELEASED BY THE NAGASAKI A-BOMB - MOBILITY IN THE ENVIRONMENT
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DOI:
10.1016/0969-8043(95)00161-6
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发表时间:
1995-11-01
影响因子:
1.6
通讯作者:
KUDO, A
中科院分区:
文献类型:
--
作者:
MAHARA, Y;KUDO, A
The first and second environmental releases of man-made Pu-239 + 240 came from nuclear explosions at Alamagordo and Nagasaki in 1945. The release at Nagasaki was more serious than at Alamagordo, because it happened in an area with a high population density. Unfissioned Pu-239 + 240 and various fission products (e.g. Sr-90 and Cs-137) have been interacting here with various environmental materials (soils, sediments, and plants) under wet and temperate conditions for more than 45 years. To assess the environmental mobility of Pu-239 + 240, the distributions of radionuclides from this release were investigated at Nishiyama (3 km east of the hypocenter) where heavy black rain containing unfissioned plutonium and fission products fell 30 minutes after the nuclear explosion. The vertical distributions of Sr-90, Cs-137 and Pu-239 + 240 were determined in unsaturated soil cores up to 450 cm deep. Most radionuclides were found in the soil column 30 cm from the ground surface (95% of Sr-90, 99% of Cs-137 and 97% of Pu-239 + 240). However, Sr-90 and Pu-239 + 240 were detected in the groundwater as well below a depth of 200 cm. No Cs-137 was found below 40 cm from the ground surface or in groundwater. These observations reveal that about 3% of the total Pu-239 + 240 has been migrating in the soil at a faster rate than the remaining Pu-239 + 240. Sharp peak of Cs-137 and Pu-239 + 240, indicating heavy deposition from the Nagasaki local fallout of 1945, were found in sediment cores collected from the Nishiyama reservoir. On the other hand, since Sr-90 is mobile in fresh water sediments, there was no 1945 Sr-90 peak in the sediment cores. Pu-239 + 240 peaks were unexpectedly discovered in pre-1945 sediment core sections. Although Sr-90 was found in these sections, no Cs-137 was found. By contrast to the distribution in sediment cores, Cs-137 in tree rings had spread by diffusion from the bark to the center of the tree without holding a fallout deposition record. Most of the Pu-239 + 240 was distributed in the tree rings following a similar deposition record to that found in sediment cores. Furthermore, a very small amount of Pu-239 + 240 (about 1%) was found unexpectedly in pre-1945 tree rings. The only reasonable explanation for these unexpected discoveries is the existence of mobile Pu-239 + 240 in the environment.