Photochemistry of Sulfur Dioxide and the Origin of Mass-Independent Isotope Fractionation in Earth's Atmosphere

被引:88
|
作者
Ono, Shuhei [1 ]
机构
[1] MIT, Dept Earth Atmospher & Planetary Sci, Cambridge, MA 02139 USA
来源
ANNUAL REVIEW OF EARTH AND PLANETARY SCIENCES, VOL 45 | 2017年 / 45卷
基金
美国国家科学基金会; 美国国家航空航天局;
关键词
Archean; early atmosphere; sulfur isotope; mass-independent fractionation; MIF; anoxic atmosphere; photolysis; SO2; sulfur dioxide; ABSORPTION CROSS-SECTIONS; MICROBIAL SULFATE REDUCTION; JET-COOLED SO2; MULTIPLE-SULFUR; DEPENDENT FRACTIONATION; DRESSER FORMATION; EARLY EVOLUTION; AB-INITIO; OXYGEN; STATE;
D O I
10.1146/annurev-earth-060115-012324
中图分类号
P1 [天文学];
学科分类号
0704 ;
摘要
Archean sulfide and sulfate minerals commonly exhibit anomalous ratios among four stable sulfur isotopes, S-32, S-33, S-34, and S-36. These anomalous relationships, referred to as sulfur mass-independent fractionation (S-MIF), provide strong evidence for an early anoxic atmosphere. Correlated variations among three isotope ratios (delta S-33, delta S-34, and delta S-36) can be observed in rocks throughout the Archean and are a key clue toward identifying the source reaction of S-MIF. Studies to investigate the origin of Archean SMIF so far have primarily focused on the photochemistry of sulfur dioxide (SO2). Photolysis of SO2 at wavelengths <220 nm and photoexcitation at 240-340 nm both yield large-magnitude S-MIF. Proposed mechanisms of S-MIF include isotopologue-dependent self-shielding, cross-sectional amplitudes, and vibronic coupling during intersystem crossing. This review discusses the emerging picture of the physical origins of S-MIF and their implications for the chemistry of the early Earth's atmosphere.
引用
收藏
页码:301 / 329
页数:29
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