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首页> 外文期刊>Earth and Planetary Science Letters: A Letter Journal Devoted to the Development in Time of the Earth and Planetary System >New insights into Archean sulfur cycle from mass-independent sulfur isotope records from the Hamersley Basin, Australia
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New insights into Archean sulfur cycle from mass-independent sulfur isotope records from the Hamersley Basin, Australia

机译:澳大利亚哈默斯利盆地质量无关的硫同位素记录对太古代硫循环的新见解

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We have measured multiple sulfur isotope ratios (~(34)S/~(33)S/~(32)S) for sulfide sulfur in shale and carbonate lithofacies from the Hamersley Basin, Western Australia. The Δ~(33)S values (Δ~(33)S ≈ δ~(33)S - 0.515 * δ~(34)S) shift from -1.9 to +6.9‰ over a 22-m core section of the lower Mount McRae Shale (~2.5 Ga). Likewise, sulfide sulfide sulfur analyses of the Jeerinah Formation (~2.7 Ga) yield Δ~(33)S values of -0.1 to +8.1‰ over a 50-m section of core. Despite wide variations in Δ~(33)S and δ~(34)S, these two shale units yield a similar positive correlation between Δ~(33)S and δ~(34)S. In contrast, pyrite sulfur analyses of the Carawine Dolomite (~2.6 Ga) yield a broad range in δ~(34)S (+3.2 to +16.2‰) but a relatively small variation and negative values in Δ~(33)S (-2.5 to -1.1‰). The stratigraphic distribution of δ~(33)S, δ~(34)S and Δ~(33)S in Western Australia allows us to speculate on the sulfur isotopic composition of Archean sulfur reservoirs and to trace pathways in the Archean sulfur cycle. Our data are explained by a combination of mass-independent fractionation (MIF) in the atmosphere and biological mass-dependent fractionation in the ocean. In the Archean, volcanic, sulfur-bearing gas species were photolysed by solar ultraviolet (UV) radiation in an oxygen-free atmosphere, resulting in MIF of sulfur isotopes. Aerosols of S_8 (with Δ~(33)S > 0) and sulfuric acid (with Δ~(33)S < 0) formed from the products of UV photolysis and carried mass-independently fractionated sulfur into the hydrosphere. The signatures of atmospheric photolysis were preserved by precipitation of pyrite in sediments. Pyrite precipitation was mediated by microbial enzymatic catalysis that superimposed mass-dependent fractionation no mass-independent atmospheric effects. Multiple sulfur isotope analyses provide new insights into the early evolution of the atmosphere and the evolution and distribution of early sulfur-metabolizing organisms.
机译:我们测量了澳大利亚西部哈默斯利盆地页岩和碳酸盐岩相中硫化物硫的多种硫同位素比(〜(34)S /〜(33)S /〜(32)S)。下部的22 m岩心段上的Δ〜(33)S值(Δ〜(33)S≈δ〜(33)S-0.515 *δ〜(34)S)从-1.9变为+ 6.9‰麦克雷页岩山(〜2.5 Ga)。同样,对杰里纳组(〜2.7 Ga)的硫化物硫化物硫分析,在岩心50 m的剖面上得出的Δ〜(33)S值为-0.1至+ 8.1‰。尽管Δ〜(33)S和δ〜(34)S差异很大,但这两个页岩单元在Δ〜(33)S和δ〜(34)S之间产生相似的正相关。相比之下,对Carawine白云石(〜2.6 Ga)的硫铁矿硫分析得出的δ〜(34)S范围较宽(+3.2至+ 16.2‰),但Δ〜(33)S的变化较小且为负值( -2.5至-1.1‰)。西澳大利亚州δ〜(33)S,δ〜(34)S和Δ〜(33)S的地层分布使我们能够推测太古代硫储层的硫同位素组成,并追踪太古代硫循环的路径。我们的数据通过大气中质量无关的分级分离(MIF)和海洋中生物质量相关的分级分离的结合来解释。在太古代中,火山中的含硫气体在无氧气氛中被太阳紫外线(UV)辐射光解,从而形成了硫同位素的MIF。 S_8(Δ〜(33)S> 0)和硫酸(Δ〜(33)S <0)的气溶胶是由UV光解产物形成的,并且将质量独立地分馏的硫带入水球。黄铁矿在沉积物中的沉淀保留了大气光解的特征。硫铁矿的沉淀是由微生物酶催化介导的,该酶催化的质量依赖性分馏没有质量依赖性的大气效应。多种硫同位素分析为大气的早期演化以及早期硫代谢生物的演化和分布提供了新的见识。

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