Anaerobic methane oxidation and the formation of dolomite

被引:139
作者
Moore, TS
Murray, RW
Kurtz, AC
Schrag, DP
机构
[1] Boston Univ, Dept Earth Sci, Boston, MA 02215 USA
[2] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02138 USA
关键词
anaerobic methane oxidation; dolomite; diagenesis;
D O I
10.1016/j.epsl.2004.10.015
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
We examine the link between organic matter degradation, anaerobic methane oxidation (AMO), and sulfate depletion and explore how these processes potentially influence dolomitization. We determined rates and depths of AMO and dolomite formation for a variety of organic-rich sites along the west African Margin using data from Ocean Drilling Program (ODP) Leg 175. Rates of AMO are calculated from the diffusive fluxes of CH4 and SO4, and rates of dolomite formation are calculated from the diffusive flux of Mg. We find that the rates of dolomite formation are relatively constant regardless of the depth at which it is forming, indicating that the diffusive fluxes of Mg and Ca are not limiting. Based upon the calculated log IAP values, log K-sp values for dolomite were found to narrowly range between -16.1 and -16.4. Dolomite formation is controlled in part by competition between AMO and methanogenesis, which controls the speciation of dissolved CO2. AMO increases the concentration of CO32- through sulfate reduction, favoring dolomite formation, while methanogenesis increases the pCO(2) of the pore waters, inhibiting dolomite formation. By regulating the pCO(2) and alkalinity, methanogenesis and AMO can regulate the formation of dolomite in organic-rich marine sediments. In addition to providing a mechanistic link between AMO and dolomite formation, our findings provide a method by which the stability constant of dolomite can be calculated in modem sediments and allow prediction of regions and depth domains in which dolomite may be forming. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 154
页数:14
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