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Multiple sulfur-isotope signatures in Archean sulfates and their implications for the chemistry and dynamics of the early atmosphere

机译:太古代硫酸盐中的多种硫同位素特征及其对早期大气化学和动力学的影响

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摘要

Sulfur isotopic anomalies (∆33S and ∆36S) have been used to trace the redox evolution of the Precambrian atmosphere and to document the photochemistry and transport properties of the modern atmosphere. Recently, it was shown that modern sulfate aerosols formed in an oxidizing atmosphere can display important isotopic anomalies, thus questioning the significance of Archean sulfate deposits. Here, we performed in situ 4S-isotope measurements of 3.2- and 3.5-billion-year (Ga)-old sulfates. This in situ approach allows us to investigate the diversity of Archean sulfate texture and mineralogy with unprecedented resolution and from then on to deconvolute the ocean and atmosphere Archean sulfur cycle. A striking feature of our data is a bimodal distribution of δ34S values at ∼+5‰ and +9‰, which is matched by modern sulfate aerosols. The peak at +5‰ represents barite of different ages and host-rock lithology showing a wide range of ∆33S between −1.77‰ and +0.24‰. These barites are interpreted as primary volcanic emissions formed by SO2 photochemical processes with variable contribution of carbonyl sulfide (OCS) shielding in an evolving volcanic plume. The δ34S peak at +9‰ is associated with non–33S-anomalous barites displaying negative ∆36S values, which are best interpreted as volcanic sulfate aerosols formed from OCS photolysis. Our findings confirm the occurrence of a volcanic photochemical pathway specific to the early reduced atmosphere but identify variability within the Archean sulfate isotope record that suggests persistence throughout Earth history of photochemical reactions characteristic of the present-day stratosphere.
机译:硫同位素异常(∆ 33 S和∆ 36 S)已被用来追踪前寒武纪大气的氧化还原演化,并记录了现代大气的光化学和输运性质。最近,研究表明在氧化性气氛中形成的现代硫酸盐气溶胶可以显示出重要的同位素异常,从而质疑太古代硫酸盐沉积的重要性。在这里,我们对3.2亿和35亿年(Ga)的硫酸盐进行了原位4S同位素测量。这种原位方法使我们能够以前所未有的分辨率研究太古代硫酸盐质地和矿物学的多样性,并从那时起使海洋和大气太古代硫酸盐循环反卷积。我们数据的一个显着特征是δ 34 S值在〜+ 5‰和+ 9‰处的双峰分布,这与现代硫酸盐气溶胶相匹配。 + 5‰处的峰代表不同年龄的重晶石,并且岩体岩性显示出∆ 33 S的变化范围在-1.77‰至+ 0.24‰之间。这些重晶石被解释为由SO2光化学过程形成的主要火山排放物,在不断演变的火山羽流中,羰基硫(OCS)屏蔽作用各不相同。 δ 34 S峰值为+ 9‰,与非 33 S异常重晶石相关,其∆ 36 S值为负,最好解释为由OCS光解形成的硫酸盐硫酸盐气溶胶。我们的发现证实了特定于早期大气还原的火山光化学途径的发生,但确定了太古硫酸盐同位素记录内的变化,表明在整个地球上存在着当今平流层特征的光化学反应。

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