脉状方解石及其流体包裹体的同位素组成:对古水文系统、构造事件和脉状形成过程的启示

Aldo Shemesh , Hagai Ron , Yigal Erel , Yehoshua Kolodny , Amos Nur
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摘要

在构造活跃区发育的第三纪脉系中测定了方解石的同位素组成及其流体包裹体的氘含量。静脉系统由三组(I、II、III)组成,各组趋势不同,通过横切关系建立了相对年龄。每组方解石δ18O-和δ 13c值都有其特征值:组1为−7.9‰,组1为+ 1.59‰;组II为−15.3‰和+ 0.54‰;ⅲ组流体包裹体δD值分别为- 15.9‰和+ 1.73‰,最老组流体包裹体δD值(ⅰ,- 23.99‰)与以色列沿海平原雨水δD值相似,最年轻组地下水δD值(ⅲ,- 49.69‰)与黑门山雨水和地下水δD值相似。我们将δD差异归因于同位素的“海拔效应”,认为水文系统的主要变化与黑门地区的山体形成和海拔有关。利用大气水δ18O和δD的关系计算了第1组(35°C)和第3组(64°C)的形成温度,表明该地区的脉状地层发生在浅埋(1.7 km)处。方解石δ13C表明脉状方解石的来源为乡村岩石,且由于压力释放,δ13C被修正了~ 1‰。基于方解石溶解度的压力依赖性和引起水力压裂和压降的孔隙压力增加循环,讨论了更一般的静脉形成模型。
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Isotopic composition of vein calcite and its fluid inclusions: Implication to paleohydrological systems, tectonic events and vein formation processes

The isotopic composition of calcite and the deuterium content of its fluid inclusions were determined in a Tertiary vein system that developed in a tectonically active region. The vein system is composed of three sets (I, II, III) with different trends and their relative age has been established by cross-cutting relations. Each set has its characteristic calcite δ18O- and δ13C-values: − 7.9 and + 1.59‰ for set 1; − 15.3 and + 0.54‰ for set II; and −15.9 and + 1.73‰ for set III, respectively, while fluid-inclusion δD of the oldest set (I, −23.99‰) resembles that of Israeli coastal plain rainwater and groundwater δD-values of the youngest set (III, −49.69‰) resemble rain- and groundwaters of Mount Hermon. We attribute the δD differences to the isotopic “altitude effect” and conclude that the major change in the hydrologic system was related to the mountain formation and the elevation of the Hermon region. Formation temperatures for set I (35°C) and set III (64°C) are calculated using the relationship between δ18O and δD of meteoric water and suggest that vein formation occurred at shallow depths (1.7 km) in this region. The calcite δ13C indicates that the country rock was the source of vein calcite and that δ13C was modified by ∼ 1‰ due to pressure release. A more general model for vein formation, based on the pressure dependence of calcite solubility and cycles of increasing pore pressure that cause hydrofracturing and pressure drop, is discussed.

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