Cross equator transport of 137Cs from North Pacific Ocean to South Pacific Ocean (BEAGLE2003 cruises)

被引:54
作者
Aoyama, M. [1 ]
Fukasawa, M. [2 ]
Hirose, K. [1 ]
Hamajima, Y. [3 ]
Kawano, T. [2 ]
Povinec, P. P. [4 ]
Sanchez-Cabeza, J. A. [5 ,6 ,7 ]
机构
[1] Meteorol Res Inst, Geochem Res Dept, Tsukuba, Ibaraki 3050052, Japan
[2] Japan Agcy Marine Earth Sci & Technol, Yokosuka, Kanagawa 2370061, Japan
[3] Kanazawa Univ, Inst Nat & Environm Technol, Low Level Radioact Lab, Nomi, Ishikawa 9231224, Japan
[4] Comenius Univ, Fac Math Phys & Informat, SK-84248 Bratislava, Slovakia
[5] Autonomous Univ Barcelona, Environm Sci & Technol Inst, Bellaterra 08193, Spain
[6] Autonomous Univ Barcelona, Dept Phys, Bellaterra 08193, Spain
[7] CIEMAT, Dept Medio Ambiente, E-28040 Madrid, Spain
关键词
SEAWATER SAMPLES; SURFACE WATERS; INDIAN OCEANS; RADIONUCLIDES; TRITIUM; SR-90; PU-239; PU-240; THROUGHFLOW; CIRCULATION; PATHWAYS;
D O I
10.1016/j.pocean.2010.12.003
中图分类号
P7 [海洋学];
学科分类号
0707 ;
摘要
The anthropogenic radionuclides such as Cs-137, Sr-90, Tc-99, I-129 and some transuranics are important tracers of transport and biogeochemical processes in the ocean. Cs-137, with a half-life of 30 years, a major fission product present in a dissolved form in seawater, is a good tracer of oceanic circulation at a time scale of several decades. At WOCE P6 line along 30 degrees S during the BEAGLE cruise in 2003, surface seawater (around 80 L) was collected a few meters below the ocean surface by a pumping system. Water column samples (from 5 to 20 L) were collected using a Rosette multisampling system and Niskin bottles. Cs-137 was separated from seawater samples using ammonium phosphomolybdate (AMP) and analysed for Cs-137 in low-level HPGe gamma-ray spectrometers. Results allowed to draw a detailed picture of the distribution of Cs-137 in the South Pacific Ocean along P6 line. A Cs-137 depth section was depicted from about 160 samples. Cs-137 concentrations in the subsurface layers ranged from 0.07 +/- 0.04 Bq m(-3) to 1.85 +/- 0.145 Bq m(-3), high in the Tasman Sea and very low in the eastern region where upwelling occurs. Water column inventories of Cs-137 from surface to 1000 dbar depth ranged from 270 +/- 104 to 1048 +/- 127 Bq m(-2). It was concluded that the source of higher Cs-137 concentration and inventories in the Tasman Sea was Cs-137 deposited in the mid latitude of the North Pacific Ocean and transported across the equator during four decades. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 16
页数:10
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