Abstract:Nishiyama district in Nagasaki is located approximately 3000 m east of the hypocenter of the atomic bomb that was dropped on 9 August 1945. This district is also known as an area where there was a concentrated radioactive fallout with the black rain that was carried by a westerly wind. The Nagasaki atomic bomb was a Pu bomb, and the fallout must have included 239Pu without fission in addition to fission products. The presence of 239Pu in Nishiyama district has been confirmed previously. In this study, the dist… Show more
“…The highest 239þ240 Pu activity concentration in surface 0e5 cm, 59.9 AE 0.81 Bq/kg (dry weight), was observed at N1 on the slope 300 m west from the Nishiyama reservoir (2.4 km east from the hypocenter). This value is comparable with the values reported before (Mahara and Miyahara, 1984;Okajima et al, 1990). The concentration decreased sharply with increasing distance from the Nishiyama reservoir, and reached the same range as global fallout Pu in surface soil of Japanese forests, 0.15e4.31 Bq/kg (dry weight) (Muramatsu et al, 2003).…”
Section: Pu Isotopes In Soilssupporting
confidence: 89%
“…1b and c. As reported in previous papers (e.g. Yamamoto et al, 1983Yamamoto et al, , 1985Okajima et al, 1990;Kudo et al, 1991), high concentrations of Pu isotopes in soils around the Nishiyama reservoir were observed. The highest 239þ240 Pu activity concentration in surface 0e5 cm, 59.9 AE 0.81 Bq/kg (dry weight), was observed at N1 on the slope 300 m west from the Nishiyama reservoir (2.4 km east from the hypocenter).…”
Section: Pu Isotopes In Soilssupporting
confidence: 81%
“…At the time of detonation of the Pu nuclear weapon over Nagasaki city on August 9, 1945, radionuclide contaminated rain, so-called ''black rain'', was deposited on the Nishiyama area, about 3 km east from the hypocenter. Several studies have demonstrated that the area was contaminated by Pu isotopes (Yamamoto et al, 1983(Yamamoto et al, , 1985Okajima et al, 1990;Kudo et al, 1991). However, the data for the 240 Pu/ 239 Pu ratio are rather scarce, and there are only limited studies describing the present situation of the contamination after 60 years from the bombing.…”
“…The highest 239þ240 Pu activity concentration in surface 0e5 cm, 59.9 AE 0.81 Bq/kg (dry weight), was observed at N1 on the slope 300 m west from the Nishiyama reservoir (2.4 km east from the hypocenter). This value is comparable with the values reported before (Mahara and Miyahara, 1984;Okajima et al, 1990). The concentration decreased sharply with increasing distance from the Nishiyama reservoir, and reached the same range as global fallout Pu in surface soil of Japanese forests, 0.15e4.31 Bq/kg (dry weight) (Muramatsu et al, 2003).…”
Section: Pu Isotopes In Soilssupporting
confidence: 89%
“…1b and c. As reported in previous papers (e.g. Yamamoto et al, 1983Yamamoto et al, , 1985Okajima et al, 1990;Kudo et al, 1991), high concentrations of Pu isotopes in soils around the Nishiyama reservoir were observed. The highest 239þ240 Pu activity concentration in surface 0e5 cm, 59.9 AE 0.81 Bq/kg (dry weight), was observed at N1 on the slope 300 m west from the Nishiyama reservoir (2.4 km east from the hypocenter).…”
Section: Pu Isotopes In Soilssupporting
confidence: 81%
“…At the time of detonation of the Pu nuclear weapon over Nagasaki city on August 9, 1945, radionuclide contaminated rain, so-called ''black rain'', was deposited on the Nishiyama area, about 3 km east from the hypocenter. Several studies have demonstrated that the area was contaminated by Pu isotopes (Yamamoto et al, 1983(Yamamoto et al, , 1985Okajima et al, 1990;Kudo et al, 1991). However, the data for the 240 Pu/ 239 Pu ratio are rather scarce, and there are only limited studies describing the present situation of the contamination after 60 years from the bombing.…”
“…The half-life of cesium-137 is relatively short (30.1y), nevertheless it is still possible to use this radionuclide for identification of source of the contamination. The main source of this isotope in the environment were the Chernobyl accident and nuclear weapon testing [17]- [20]. The 239,240 Pu/ 137 Cs activity ratio of 0.018 and 238 Pu/ 137 Cs activity ratio of 0.00068 the representative value of global fallout in soil were determined by Bunzl and Kracke in 1988 [21].…”
“…A review article entitled "Plutonium in the Environment" (Harley6» stimulated studies for Nagasaki. Yamamoto et al7> and Okajima et al 8 ) measured plutonium concentrations in environmental samples around the city of Nagasaki and found that there were some elevated levels of 239+24~and 137CS. They were, however, not able to recognize the degree of scientific importance of the radioactive residues from the first Pu A-bomb explosion with a human loss.…”
Section: Introduction a Nagasaki A-bomb And Sciencementioning
An artificial single dose contaminant was released at Nagasaki, Japan on August 9, 1945 detonating plutonium (10-15 kg) atomic bomb. A portion, 1.2 kg of 23~was fissioned releasing 21 kt TNT energy along with various fission products. The rest of the unexpended fissile material, 239+24~, 13.8 kg (3.49 x 1013 Bq), was dispersed into the atmosphere along with a fission product, 137CS, 23.4 g (7.44 x 1013 Bq). The fate of 239+24~and 137CS was investigated by analysing both local and global fallout.The highest concentration of 239+24~was 64.5 mBq/g (181 mBq/cm 2 ) while it was 188 mBq/g (526 mBq/cm 2 ) for 137CS both at 2.8 km east from the hypocentre. The total amount of deposition in the local fallout region of 264 km 2 was 37.5 g (9.48 xl0 1 0Bq) for 239+24~and 3.14 mg (5.88 x 10 10 Bq) for 137CS. The ratio of the local fallout against the total amount of the radionuclides released was 0.27 % for 239+24~and 0.134 % for 137CS.Recent advancements in analytical technology made it possible for artificial radionuclides released from the Nagasaki explosion to be detected in the Arctic ice core layer of 1945. The 239+24~and the 137CS, were measured by collecting 10 ice cores on the Agassiz ice cap, Ellesmere Island, Canada. The deposition was 0.16 JlBq/cm 2 for 239+24~and 20 JlBq/cm 2 for 131CS. During the atmospheric testing, the deposition of 239+24OpU and 131CS varied more than 100 times with the highest peaks of over 50 JlBq/cm 2 for 239+24~and over 800 JlBq/cm 2 for 137CS both occurred in 1962. Analyzing Arctic data, there are many new information for long global transport, the history of nuclear weapons development etc.
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