Isotopic composition of salt crusts in Saskatchewan, Canada

G.N. Dowuona , A.R. Mermut , H.R. Krouse
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Abstract

The source of sulfate salts in the Great Plains region of North America is not well understood. Sulfur and oxygen isotope data of sulfate salt efflorescences and other sulfur-bearing species from selected locations in Saskatchewan were used to understand the sources, mechanism of formation and association of these salts with different facies of the sedimentary rocks in the area. The δ34SSO42 and δ18OSO42-values of the solid salt samples varied widely and ranged from −42.9 to 10.5‰ and −8.3 to +15.1‰, respectively. The δ34S-values of the pyrite, coal, jarosite and gypsum samples also ranged from −39.0 + 4.0‰. The δ18O-values of the jarosite and gypsum samples varied between −10.3 and +14.4‰, indicating their close relationships with the salt crusts. Oxidation of pyrite and hydrolysis of natrojarosite appear to play a major role in the salt formation. The very low negative δ34S-values associated with Cretaceous marine shales suggest a bacterial SO42− reduction during the formation of pyrite at the bottom of the sea (pelagic facies), which once occupied the area. The salts with positive δ18O-values are associated with Tertiary continental environment and are consistent with the high sulfur isotopic composition of coal samples in this sediment. This suggests that the δ34S-values depend on the type of lithofacies of the sediment and can be utilized to establish the formation conditions of sulfur species. The positive δ18O-values of majority of the salt crust samples indicate an incorporation of greater amount of atmospheric oxygen into the SO42−, hence a drier (semi-arid) environment during their formation, than for those salts with negative values, which are likely formed under a more humid environment or regions with high moisture regimes in the landscape. The oxygen isotopic composition of the salt crust from Chaplin Lake showed that incorporation of oxygen from the atmosphere into the sulfate was far more significant than salts from the rest of the study sites.

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加拿大萨斯喀彻温省盐壳的同位素组成
北美大平原地区硫酸盐的来源尚不清楚。利用萨斯喀彻温省选定地点的硫酸盐盐和其他含硫物种的硫氧同位素数据,了解这些盐的来源、形成机制以及与该地区不同沉积岩相的联系。固体盐样品的δ34SSO42和δ 18oso42值变化较大,分别为- 42.9 ~ 10.5‰和- 8.3 ~ +15.1‰。黄铁矿、煤、黄钾铁矾和石膏样品的δ 34s值也在- 39.0 + 4.0‰之间。黄钾铁矾和石膏的δ 18o值在−10.3 ~ +14.4‰之间变化,表明它们与盐壳关系密切。黄铁矿的氧化和钠黄钾铁矾的水解似乎在盐的形成中起主要作用。与白垩纪海相页岩相关的极低负δ 34s值表明,在海底(远洋相)黄铁矿形成过程中,细菌SO42−减少了,黄铁矿曾经占据了该地区。δ 18o值为正的盐类与第三纪大陆环境有关,与该沉积物中煤样的高硫同位素组成一致。这表明,δ 34s值与沉积岩相类型有关,可以用来确定硫种的形成条件。大多数盐壳样品的正δ 18o值表明,与那些可能在更潮湿的环境或景观中湿度较高的地区形成的负δ 18o值相比,它们在SO42−中加入了更多的大气氧,因此在形成过程中处于更干燥(半干旱)的环境。卓别林湖盐壳的氧同位素组成表明,大气中的氧与硫酸盐的结合远比其他研究地点的盐要重要得多。
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