Early diagenesis of organic-matter-rich sediments in a ria environment: Organic matter sources, pyrites morphology and limitation of pyritization at depth

被引:34
作者
Alvarez-Iglesias, P. [1 ]
Rubio, B. [1 ]
机构
[1] Univ Vigo, Fac Marine Sci, Dept Marine Geosci & Land Use Management, Vigo 36310, Pontevedra, Spain
关键词
diagenesis; organic-matter-rich sediments; C/N; carbon isotopes; pyrites; DOP; Spain; Ria de Vigo; SIMON BAY RIA; IRON II MONOSULFIDE; NW SPAIN; DE-VIGO; INTERTIDAL SEDIMENTS; SUBTIDAL SEDIMENTS; METAL CONCENTRATIONS; ISOTOPIC COMPOSITION; SULFUR SPECIATION; FRAMBOIDAL PYRITE;
D O I
10.1016/j.ecss.2012.01.005
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
The subtidal sediments of the inner Ria de Vigo (NW Spain) are fine-grained, rich in organic matter, and accumulate at rates of around 3 mm/yr. Redoxomorphic pyrites formation was studied in four sediment cores. Four operationally-defined iron fractions were determined (HCl-extracted, silicate-bound, organic and pyritic), and the dimensions and morphology of pyrites (which mainly occurred as isolated framboids 3-5 mu m in diameter) were studied by SEM. Sediment appearance and degree of pyritization (DOP) identified an oxic zone limited to the top few millimetres, a suboxic zone that in most cores was just a few decimetres thick (the exception was a core obtained in an area of strong turbulent currents), and an underlying anoxic zone with DOP values of around 60%. Pyritic iron increased at the expense of the HCl-extracted fraction in approximately the top metre, but no further pyrite formation occurred at greater depths. Pyrite formation in these lower levels was not limited by lack of either HCl-extracted iron or metabolizable organic matter, but apparently by lack of sulphate ion, the diffusion of which to these depths was probably prevented by the fine texture of the sediments. Our findings highlight the interest of studying transitional sedimentary environments in order to explore in detail the geochemical parameters controlling pyrite formation. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:113 / 123
页数:11
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