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Sulfur and oxygen isotopes in the gypsum deposits of the Provalata sulfuric acid cave (Macedonia)

机译:Provalata硫酸洞穴(马其顿)的石膏沉积物中的硫和氧同位素

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Sulfur stable isotopes from cave sulfates (mainly gypsum) have been used in a number of studies to trace the source of sulfur in caves formed by sulfuric acid, but only few studies apply combined use of sulfur and oxygen stable isotopes to further understand the processes operating in sulfuric acid speleogenesis (SAS). Here we present results of a detailed study of the distribution of sulfur and oxygen stable isotopes within the gypsum deposits formed during sulfuric acid speleogenesis of Provalata Cave (Macedonia). The delta O-18 (vs VSMOW) values range between -3.9 parts per thousand and +8.2 parts per thousand, and the delta S-34 (vs CDT) values between -7.5 parts per thousand and +0.7 parts per thousand. We found a strong positive correlation between the delta O-18 and delta S-34 values, with a 0.5 parts per thousand increase in the delta S-34 for every 1 parts per thousand increase in the delta O-18, indicating that both oxygen and sulfur isotopes were concurrently affected during the oxidation process. We attribute these effects to be either due to environmental control (concentrations of H2S and O-2) or due to isotope fractionation during multi-step microbial oxidation, also affected by the environmental conditions. Additionally a shift of +1.85 parts per thousand in the delta S-34 values prior to the H2S oxidation is found, indicating evolution of the H2S delta S-34 in the SAS system. The wide range of both delta O-18 and delta S-34 values in the gypsum deposits of the small Provalata Cave show that both the number of samples and their location can be an important factor for the understanding of sulfuric acid speleogenesis using stable isotopes. (C) 2018 Elsevier B.V. All rights reserved.
机译:来自洞穴硫酸盐(主要是石膏)的硫稳定同位素已用于许多研究中,以追踪由硫酸形成的洞穴中的硫源,但只有很少的研究将硫和氧稳定同位素结合使用以进一步了解操作过程在硫酸形成过程中(SAS)。在这里,我们介绍了在Provalata Cave(马其顿)的硫酸星团形成过程中形成的石膏沉积物中,硫和氧稳定同位素分布的详细研究结果。增量O-18(vs VSMOW)值在-3.9千分之内和+8.2千分之内,而S-34(vs CDT)增量在-7.5千分之几和+0.7千分之二之间。我们发现增量O-18和增量S-34值之间存在很强的正相关关系,增量O-18每增加千分之一,增量S-34就会增加0.5千分之多,这表明氧硫同位素在氧化过程中同时受到影响。我们将这些影响归因于环境控制(H2S和O-2的浓度),或者归因于多步微生物氧化过程中的同位素分馏,也受到环境条件的影响。另外,在硫化氢氧化之前,δS-34值每千分之几+1.85位移,这表明SAS系统中硫化氢δS-34的演变。小Provalata洞穴的石膏矿床中的δO-18和δS-34值范围很广,表明样品的数量及其位置都是理解使用稳定同位素进行硫酸成因的重要因素。 (C)2018 Elsevier B.V.保留所有权利。

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