137Cs, 239+240Pu and 240Pu/239Pu atom ratios in the surface waters of the western North Pacific Ocean, eastern Indian Ocean and their adjacent seas.

Surface seawater samples were collected along the track of the R/V Hakuho-Maru cruise (KH-96-5) from Tokyo to the Southern Ocean. The (137)Cs activities were determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas, the eastern Indian Ocean, the Bay of Bengal, the Andaman Sea, and the South China Sea. The (137)Cs activities showed a wide variation with values ranging from 1.1 Bq m(-3) in the Antarctic Circumpolar Region of the Southern Ocean to 3 Bq m(-3) in the western North Pacific Ocean and the South China Sea. The latitudinal distributions of (137)Cs activity were not reflective of that of the integrated deposition density of atmospheric global fallout. The removal rates of (137)Cs from the surface waters were roughly estimated from the two data sets of Miyake et al. [Miyake Y, Saruhashi K, Sugimura Y, Kanazawa T, Hirose K. Contents of (137)Cs, plutonium and americium isotopes in the Southern Ocean waters. Pap Meteorol Geophys 1988;39:95-113] and this study to be 0.016 yr(-1) in the Sulu and Indonesian Seas, 0.033 yr(-1) in the Bay of Bengal and Andaman Sea, and 0.029 yr(-1) in the South China Sea. These values were much lower than that in the coastal surface water of the western Northwest Pacific Ocean. This was likely due to less horizontal and vertical mixing of water masses and less scavenging. (239+240)Pu activities and (240)Pu/(239)Pu atom ratios were also determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas and the South China Sea. The (240)Pu/(239)Pu atom ratios ranged from 0.199+/-0.026 to 0.248+/-0.027 on average, and were significantly higher than the global stratospheric fallout ratio of 0.18. The contributions of the North Pacific Proving Grounds close-in fallout Pu were estimated to be 20% for the western North Pacific Ocean, 39% for the Sulu and Indonesian Seas and 42% for the South China Sea by using the two end-member mixing model. The higher (240)Pu/(239)Pu atom ratios could be attributed to close-in fallout Pu delivered from the Enewetak and Bikini Atolls by ocean currents of branches of the North Equatorial Current to the Southeast Asian seas.

[1]  Kiyoshi Nakamura,et al.  239, 240Pu,137Cs and90Sr in the central North Pacific , 1984 .

[2]  M. Aoyama,et al.  Analysis of 137Cs and 239,240Pu concentrations in surface waters of the Pacific Ocean , 2003 .

[3]  R. Anderson,et al.  Large particle transport of plutonium and other fallout radionuclides to the deep ocean , 1983, Nature.

[4]  Masatoshi Yamada,et al.  Sediment core record of global fallout and Bikini close-in fallout Pu in Sagami Bay, Western Northwest Pacific margin. , 2004, Environmental science & technology.

[5]  Ken O. Buesseler,et al.  The isotopic signature of fallout plutonium in the North Pacific , 1997 .

[6]  Bo Qiu,et al.  Kuroshio And Oyashio Currents , 2001 .

[7]  S. Godfrey Indonesian Throughflow And Leeuwin Current , 2001 .

[8]  裕之 長屋,et al.  北太平洋中部の239, 240Pu, 137Csおよび90Srの分布 , 1984 .

[9]  P. Povinec,et al.  90Sr, 137Cs and (239,240)Pu concentration surface water time series in the Pacific and Indian Oceans--WOMARS results. , 2005, Journal of environmental radioactivity.

[10]  Yoshihiro Ikeuchi,et al.  IAEA’97 expedition to the NW Pacific Ocean—results of oceanographic and radionuclide investigations of the water column , 2003 .

[11]  M. Yamada,et al.  Temporal variations of137Cs concentrations in the surface seawater and marine organisms collected from the Japanese coast during the 1980's , 1998 .

[12]  Kiyoshi Nakamura,et al.  Artificial radionuclides in the western Northwest Pacific (I)90Sr and137Cs in the deep waters , 1981 .

[13]  岩崎 民子 SOURCES AND EFFECTS OF IONIZING RADIATION : United Nations Scientific Committee on the Effects of Atomic Radiation UNSCEAR 2000 Report to the General Assembly, with Scientific Annexes , 2002 .

[14]  S. Fowler,et al.  Vertical transport of particulate-associated plutonium and americium in the upper water column of the Northeast Pacific , 1983 .

[15]  T. Beasley,et al.  Global distribution of Pu isotopes and 237Np. , 1999, The Science of the total environment.

[16]  R. Lukas Pacific Ocean Equatorial Currents , 2001 .

[17]  V. T. Bowen,et al.  Fallout radionuclides in the Pacific Ocean: Vertical and horizontal distributions, largely from GEOSECS stations , 1980 .

[18]  G. Hong,et al.  Plutonium isotopes in seas around the Korean Peninsula. , 2004, The Science of the total environment.

[19]  Edward D. Goldberg,et al.  The240Pu239Pu ratio, a potential geochronometer , 1985 .

[20]  Karl K. Turekian,et al.  Encyclopedia of Ocean Sciences , 2001 .

[21]  P. Povinec,et al.  Spatial distribution of 3H, 90Sr, 137Cs and (239,240)Pu in surface waters of the Pacific and Indian Oceans--GLOMARD database. , 2004, Journal of environmental radioactivity.

[22]  Masatoshi Yamada,et al.  Plutonium activities and 240Pu/239Pu atom ratios in sediment cores from the east China sea and Okinawa Trough: Sources and inventories , 2005 .

[23]  H. Métivier,et al.  Radionuclides in the oceans : inputs and inventories , 1996 .

[24]  239+240Pu and137Cs distributions in seawater from the Yamato Basin and the Tsushima Basin in the Japan Sea , 1996 .

[25]  M. Kennish,et al.  Practical Handbook of Marine Science , 1988 .

[26]  Glenn T. Seaborg,et al.  Heavy Isotope Abundances in Mike Thermonuclear Device , 1960 .

[27]  Masatoshi Yamada,et al.  Inductively coupled plasma-sector field mass spectrometry with a high-efficiency sample introduction system for the determination of Pu isotopes in settling particles at femtogram levels. , 2006, Talanta.

[28]  Kiyoshi Nakamura,et al.  Artificial radionuclides in the western Northwest Pacific (II):137Cs and239,240Pu inventories in water and sediment columns observed from 1980 to 1986 , 1987 .

[29]  P. Povinec,et al.  Anthropogenic radionuclides in Indian Ocean surface waters—the Indian Ocean transect 1998 , 2003 .

[30]  酒井 均,et al.  Biogeochemical processes and ocean flux in the Western Pacific , 1995 .

[31]  T. Aono,et al.  Large particle flux of 239+240Pu on the continental margin of the East China Sea. , 2002, The Science of the total environment.

[32]  Chih-An Huh,et al.  Sedimentation in the Southern Okinawa Trough: enhanced particle scavenging and teleconnection between the Equatorial Pacific and western Pacific margins , 2004 .

[33]  Y. Nagaya,et al.  Distributions and mass-balance of 239,240Pu and 137Cs in the northern North Pacific , 1993 .

[34]  F. Pointurier,et al.  240Pu/239Pu isotopic ratios and 239 + 240Pu total measurements in surface and deep waters around Mururoa and Fangataufa atolls compared with Rangiroa atoll (French Polynesia). , 1999, The Science of the total environment.

[35]  A. Aarkrog Input of anthropogenic radionuclides into the World Ocean , 2003 .

[36]  Masatoshi Yamada,et al.  Vertical distributions of 239+240Pu activities and 240Pu/239Pu atom ratios in sediment cores: implications for the sources of Pu in the Japan Sea. , 2005, The Science of the total environment.

[37]  Edward D. Goldberg,et al.  Plutonium isotopes in the environment: some existing problems and some new ocean results , 1986 .

[38]  Y. Sugimura,et al.  Contents of 137Cs, plutonium and americium isotopes in the Southern Ocean waters. , 1988 .