New Constraints on Precambrian Ocean Composition

石盐 石膏 地质学 前寒武纪 蒸发岩 海水 硬石膏 地球化学 碳酸盐 文石 方解石 太古宙 降水 矿物学 海洋学 古生物学 沉积岩 化学 有机化学 气象学 物理
作者
J. Grotzinger,James F. Kasting
出处
期刊:The Journal of Geology [University of Chicago Press]
卷期号:101 (2): 235-243 被引量:408
标识
DOI:10.1086/648218
摘要

The Precambrian record of carbonate and evaporite sedimentation is equivocal. In contrast to most previous interpretations, it is possible that Archean, Paleoproterozoic, and to a lesser extent, Meso to Neoproterozoic seawater favored surplus abiotic carbonate precipitation, as aragonite and (hi-Mg?) calcite, in comparison to younger times. Furthermore, gypsum/anhydrite may have been only rarely precipitated prior to halite precipitation during evaporation prior to about 1.8 Ga. Two effects may have contributed to these relationships. First, sulfate concentration of seawater may have been critically low prior to about 1.9 Ga so the product $$m_{Ca^{++}}\cdot m_{SO^{--}}$$ would not have produced gypsum before halite, as in the Mesoproterozoic to modern ocean. Second, the bicarbonate to calcium ratio was sufficiently high so that during progressive evaporation of seawater, calcium would have been exhausted before the gypsum field was reached. The pH of the Archean and Paleoproterozoic ocean need not have been significantly different from the modern value of 8.1, even at $$CO_{2}$$ partial pressures of a tenth of an atmosphere. Higher $$CO_{2}$$ partial pressures require somewhat lower pH values.

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