质量无关分馏
太古宙
硫黄
分馏
硫酸盐
硫同位素
环境化学
缺氧水域
同位素分馏
大气(单位)
元古代
同位素特征
化学
硫循环
δ34S
同位素
地质学
地球化学
古生物学
热液循环
蛋氨酸
流体包裹体
氨基酸
构造学
生物化学
量子力学
热力学
物理
有机化学
作者
Alexander A. Pavlov,James F. Kasting
出处
期刊:Astrobiology
[Mary Ann Liebert, Inc.]
日期:2002-03-01
卷期号:2 (1): 27-41
被引量:882
标识
DOI:10.1089/153110702753621321
摘要
Mass-independent fractionation (MIF) of sulfur isotopes has been reported in sediments of Archean and Early Proterozoic Age (> 2.3 Ga) but not in younger rocks. The only fractionation mechanism that is consistent with the data on all four sulfur isotopes involves atmospheric photochemical reactions such as SO2 photolysis. We have used a one-dimensional photochemical model to investigate how the isotopic fractionation produced during SO2 photolysis would have been transferred to other gaseous and particulate sulfur-bearing species in both low-O2 and high-O2 atmospheres. We show that in atmospheres with O2 concentrations < 10(-5) times the present atmospheric level (PAL), sulfur would have been removed from the atmosphere in a variety of different oxidation states, each of which would have had its own distinct isotopic signature. By contrast, in atmospheres with O2 concentrations > or = 10(-5) PAL, all sulfur-bearing species would have passed through the oceanic sulfate reservoir before being incorporated into sediments, so any signature of MIF would have been lost. We conclude that the atmospheric O2 concentration must have been < 10(-5) PAL prior to 2.3 Ga.
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