Speciation and spatial distribution of solid-phase iron in surface sediments of the East China Sea continental shelf

被引:67
|
作者
Zhu, Mao-Xu [1 ]
Hao, Xiao-Chen
Shi, Xiao-Ning
Yang, Gui-Peng
Li, Tie
机构
[1] Ocean Univ China, Coll Chem & Chem Engn, Qingdao 266100, Peoples R China
基金
美国国家科学基金会;
关键词
SULFIDE MINERAL FORMATION; ORGANIC-CARBON; SULFATE REDUCTION; YANGTZE-RIVER; BUFFERING CAPACITY; ISOTOPIC COMPOSITIONS; COASTAL SEDIMENTS; FE(III) REDUCTION; MARINE-SEDIMENTS; EARLY DIAGENESIS;
D O I
10.1016/j.apgeochem.2012.01.004
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Speciation and reactivity characterization of solid-phase Fe in marine sediments are of significance to understanding its heterogeneous mineralogy and crystallinity, the diagenetic cycling of Fe and its regulating roles on many other elements in sediments. In this study, a combination of sequential and single-step extractions was used for the determination of seven Fe pools in surface sediments of the East China Sea (ECS) continental shelf: (1) carbonate associated Fe (Fe(II)(carb)) plus acid volatile sulfide-Fe (Fe(II)(AVS)), (2) easily reducible amorphous/poorly crystalline Fe oxides (Fe-ox1), (3) reducible crystalline Fe oxides (Fe-ox2), (4) magnetite (Fe-mag), (5) poorly reactive sheet silicate Fe (Fe-PRS), (6) pyrite-Fe (Fe-py), and (7) unreactive silicate Fe (Fe-U). Total Fe (Fe-T) in the sediments is largely determined by terrestrial aluminosilicate particles as indicated by a great similarity of the Fe-T with that of the Yangtze River and global riverine particulates. The size of Fe-PRS is found to be the largest pool, followed by Fe-U, Fe-ox2, Fe-mag, Fe(II)(AVS+carb), Fe-ox1 and Fe-py. The large Fe-PRS may result from neoformation of Fe-rich clay minerals via reverse weathering and subsequent ageing. The small sizes of Fe(II)(AVS+carb) and Fe-py pools is believed to be the result of low SO4 reduction due to generally low labile organic matter together with the oxic/suboxic, dynamic environments of the surface sediments. The occurrence of Fe-ox1, Fe-ox2 and Fe-PRS in the sediments is closely associated with the clay fraction as indicated by a high spatial correlation between the former and the latter. Highly reactive Fe(Fe-HR) in the sediments is comparable to that in global marine sediments, but apparently lower than in the Yangtze River and global riverine particulates due probably to sequestration in the Yangtze Estuary. The ratios of Fe-HR/Fe-T, Fe-PR/Fe-T and Fe-U/Fe-T in the ECS surface sediments consistently show more similarity to those in the Yangtze River particulates than in the global continental margin or deep-sea sediments. The surface sediments maintain a high level of buffering capacity toward sulfidation suggested by a large fraction of highly reactive Fe(III) oxides (Fe(III)(HR)) in Fe-HR. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:892 / 905
页数:14
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