Early diagenetic redistribution and burial of phosphorus in the sediments of the Southwestern East Sea (Japan Sea)

被引:99
作者
Cha, HJ [1 ]
Lee, CB
Kim, BS
Choi, MS
Ruttenberg, KC
机构
[1] Korea Atom Energy Res Inst, Nucl Environm Res Div, Taejon 305600, South Korea
[2] Seoul Natl Univ, Sch Earth & Environm Sci, Seoul 151747, South Korea
[3] Med Univ Gdansk, Coll Pharm, Dept Food Sci, Gdansk, Poland
[4] Chungnam Natl Univ, Dept Oceanog & Ocean Environm Sci, Taejon 305764, South Korea
[5] Univ Hawaii, Sch Ocean & Earth Sci & Technol, Dept Geol & Geophys, Dept Oceanog, Honolulu, HI 96822 USA
关键词
phosphorus; early diagenesis; redistribution; Fe oxides; carbonate fluorapatite; burial flux; sedimentation rate;
D O I
10.1016/j.margeo.2005.02.001
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
This study was carried out in order to understand the early diagenetic redistribution of phosphorus and relevant mass balance in the sediments of the East Sea. In two cruises during May 1993 and October 1995, 11 box cores were collected in the southwestern part of the East Sea. Dissolved phosphorus and iron were analyzed in the porewater from the cores. Sediment samples were analyzed for solid-phase P species and solid-phase Fe oxyhydroxide by sequential extraction. Phosphorus speciation results show that organic P is the major chemical form of phosphorus in young sediments within the upper 50 cm of sediment. However, the authigenic fraction of total P increases with depth, indicating the precipitation of carbonate fluorapatite (CFA) in the sediments. The authigenic CFA (Ca-5(PO4)(2.6)(CO3)(0.4)F) was formed and buried at rates of 11-110 mu mol cm(-2) kyr(-1). The main source of dissolved phosphorus for the precipitation of CIA is organic P. Dissolved phosphorus, released from the decomposition of organic P, diffuses upward to return to bottom water, or is sorbed to iron oxides in the oxidized sediments. As sedimentation proceeds, the iron oxide-bound P is released in the reduced layer and enters the dissolved phase, which contributes P to the formation of CIA in addition to that contributed by the organic P. The burial flux of reactive P (iron oxide-bound P+authigenic P+organic P) is 0.09-0.53 g p m(-2) yr(-1) that accounts for 18-58% of the reactive P arriving at the sediment/water interface. The burial flux of reactive P is high in the upper and lower continental margin sediment. The burial flux of reactive P in the Ulleung Basin sediment is less than those in the continental margin sites by a factor of 6, indicating that the reactive P burial flux is mainly dependent on sedimentation rate. (c) 2005 Elsevier B.V. All rights reserved.
引用
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页码:127 / 143
页数:17
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