Geochemical features of Eurasian evaporites in the context of the chemical evolution of seawater in Phanerozoic

Аnatolіy R. Galamay, A. Poberezhskyy, S. Hryniv, S. Vovnyuk, Dariya Sydor, I. Iaremchuk, Sofiya Maksymuk, Oksana Oliyovych-Hladka, Lyudmila Bilyk
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Abstract

Studies of evaporites provide new data to characterize the seawater chemistry in the Early Paleozoic and Middle Mesozoic. In particular, we studied the fluid inclusions in halite from Ordovician (China) and Cretaceous (Laos) evaporites. The corresponding sections on the plot of Ca/SO4 oscillations curve in the Phanerozoic seawater are updated. The calcium content in seawater concentrated to halite precipitation stage was 45.6 mol %, 485 million years ago and 24.3 mol % 112.2–93.5 million years ago. By analyzing the previously published and new factual material, it is established that in Permian evaporites the sulfur isotopic composition is inversely correlated with the sulfate ion content in evaporite basin brines. Thus, the evolution of seawater chemistry in Permian is confirmed by the evolution of the isotopic composition of dissolved seawater sulfate. According to the generalization of 38 Phanerozoic marine evaporite formations, it was found that the peculiarities of the clay minerals associations correlate with the change of the seawater chemical type. Clay minerals associations precipitated from the SO4-rich seawater are characterized by a larger set of minerals, among which smectite and mixed-layered minerals often occur; Mg-rich clay minerals (corensite, paligorskite, sepiolite, talc) also occur. Instead, in the associations of evaporite clay minerals formed from the Ca-rich seawater are represented by the smaller amount of minerals, and Mg-rich minerals are extremely rare. The increased content of magnesium in seawater of SO4-rich type is the main factor in the formation of Mg-rich silicates in evaporites. The composition of clay minerals associations depends on the evaporate basin brine concentration; with its increase, unstable minerals are transformed, which theoretically leads to a decrease in the number of minerals in the associations. However, it was found that evaporite deposits of higher stages of brine concentration often still contain unstable clay minerals – products of incomplete transformation of a significant amount of pyroclastic material from coeval volcanic activity. The main factor determining the composition of clay minerals associations of Phanerozoic evaporites was the seawater (and basin brines) chemical type. Geochemical studies of scattered organic matter and fluid inclusions with hydrocarbon phase in evaporites of the Upper Pechora Basin (overlying oil and gas deposits) indicate the presence of allochthonous bitumoids and allow to use this method to predict oil and gas potential of other areas. Analysis of the results of oil and gas exploration in a number of areas of the Transcarpathian Trough indicates the presence of fluid-saturated reservoirs and the prospects for the discovery of new accumulations of hydrocarbons. Geochemical studies proved the effectiveness of gas-flow survey method for oil and gas exploration, assessing the prospects for fluid saturation of seismic structures.
显生宙海水化学演化背景下欧亚大陆蒸发岩地球化学特征
蒸发岩的研究为表征早古生代和中中生代的海水化学提供了新的资料。重点研究了中国奥陶系和老挝白垩系蒸发岩中岩盐岩的流体包裹体。更新了显生宙海水Ca/SO4振荡曲线图的相应剖面。4.85亿年前海水中钙含量为45.6% mol %, 1.122 ~ 9350万年前海水中钙含量为243% mol %。通过对已有文献和新的事实资料的分析,确定了二叠纪蒸发岩中硫同位素组成与蒸发岩盆地卤水中硫酸盐离子含量呈负相关关系。因此,二叠纪海水化学的演化可以通过溶解海水硫酸盐同位素组成的演化得到证实。通过对38个显生宙海相蒸发岩组的综合分析,发现黏土矿物组合的特殊性与海水化学类型的变化有关。从富so4海水中沉淀的粘土矿物组合具有矿物种类较多的特点,其中常出现蒙脱石和混层矿物;也有富镁的粘土矿物(钙长石、硅长石、海泡石、滑石)。相反,在富钙海水形成的蒸发岩黏土矿物组合中,矿物数量较少,富镁矿物极为罕见。富so4型海水中镁含量的增加是蒸发岩中富镁硅酸盐形成的主要因素。黏土矿物组合的组成取决于蒸发盆地卤水浓度;随着它的增加,不稳定的矿物质被转化,这在理论上导致组合中矿物质数量的减少。然而,研究发现,较高阶段卤水浓度的蒸发岩矿床往往仍含有不稳定的粘土矿物——同时期火山活动产生的大量火山碎屑物质不完全转化的产物。显生宙蒸发岩粘土矿物组合组成的主要因素是海水(和盆地盐水)化学类型。对上佩科拉盆地(上覆油气矿床)蒸发岩中散在有机质和含烃流体包裹体的地球化学研究表明,异源沥青的存在,为利用该方法预测其他地区的油气潜力提供了依据。对喀尔巴阡海槽若干地区的石油和天然气勘探结果的分析表明,存在流体饱和的储层,并有发现新的碳氢化合物聚集的前景。地球化学研究证明了气流量测量方法在油气勘探中的有效性,评价了地震构造流体饱和度的前景。
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