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Geochemical Evolution of Fracture Filling Minerals from the Chalk River Laboratory Site, Ontario, Canada

机译:加拿大安大略省粉笔河实验室现场的裂缝填充矿物的地球化学演化

摘要

The isotope geochemistry combined with fluid inclusion studies of several generations of fracture minerals from the Chalk River Laboratory site (CRL) has been applied to investigate the past fluid evolution including hydrothermal processes and hydrogeochemical evolution of the rock mass. Typical fracture minerals found at the CRL site include chlorite, quartz, dolomite, and calcite. Fracture mineral investigations use oxygen and carbon isotopes from calcites combined with fluid inclusion information such as homogenization temperatures (Th), and melting temperatures (Tm) to calculate temperature and salinity of calcite forming fluids. By combining Th with oxygen isotopic data, we were able to use δ18O geothermometry calculations to estimate past isotopic characteristics and composition of the fluids responsible for calcite precipitation. From petrologic evidence, calcite from the CRL site mainly includes four varieties: fibrous calcite, metasomatic calcite, crystal calcite, and vuggy calcite. Fibrous calcite precipitated at a temperature of 78 to 128 oC with a δ13C signature of -4.91 to -7.88 ‰ (VPDB) and a δ18O signature of -9.36 to -17.34 ‰ (VPDB). These calcites were formed at an elevated temperature, in a low salinity, Na-Cl fluid that could have been a mixture of hydrothermal water derived from meteoric fluids or seawater. Metasomatic calcite precipitated at 62.1 to 90.0 oC with a δ13C signature of -4.64 to -8.59 ‰ (VPDB) and a δ18O signature of -11.98 to -15.08 ‰ (VPDB). These fluids were elevated in temperature, had higher salinity and a Ca-Na-Cl composition similar to a sedimentary basinal brine. Crystal calcite separated into three groups according to fluid inclusion analyses and results, which are (a) elevated-temperature (67 to 113 oC) low-salinity calcite (lower than 15.14 wt. %), (b) elevated-temperature (73.7 to 91.7 oC) high-salinity (30 to 40 wt. %) calcite, and (c) higher-temperature (179.6 to 199 oC) low-salinity (lower than 7.33 wt. %) calcite. Group (a) has a δ13C isotopic signature of -5.61 to -10.42 ‰ (VPDB) and a δ18O signature of -8.35 to -16.04 ‰ (VPDB), Group (b) has a δ13C isotopic signature of -4.64 to -8.60 ‰ (VPDB) and a δ18O signature of -12.34 to -15.04 ‰ (VPDB), and Group (c) has δ13C signature of -5.59 to -8.06 ‰ (VPDB) and a δ18O signature of -10.03 to -16.17 ‰ (VPDB). Group (a) most likely formed from a hydrothermal fluid with a meteoric water origin, Group (b) could have formed during hydrothermal fluid mixing with an evaporated seawater or basinal brine, and group (c) seems to have formed as a result of a mixture of meteoric and lower salinity metamorphic or crystalline rock fluids. Vuggy calcite precipitated at 85 to 89 oC with a δ13C signature of -7.47 to -9.04 ‰ (VPDB) and a δ18O signature of -9.32 to -10.59 ‰ (VPDB). This case is from a high temperature, high Ca-Na-Cl salinity fluid which is hydrothermal fluids mixed with basinal brines. Strontium isotopic ratios, thorium-uranium ratios and REE data associated with the fracture calcites show that they have a limited water/rock interaction with the host bedrock. Some elevated thorium or uranium concentration were sourced from specific rock types such as pegmatite intrusions in the site.
机译:同位素地球化学与粉笔河实验室站点(CRL)的几代压裂矿物的流体包裹体研究相结合,已用于研究过去的流体演化,包括岩浆的热液过程和水地球化学演化。在CRL现场发现的典型压裂矿物包括绿泥石,石英,白云石和方解石。断裂矿物研究使用方解石中的氧和碳同位素,结合流体包裹体信息(例如均质温度(Th)和熔化温度(Tm))来计算方解石形成液的温度和盐度。通过将Th与氧同位素数据结合起来,我们能够使用δ18O地热法计算来估算过去的同位素特征和引起方解石沉淀的流体成分。根据岩石学证据,CRL站点的方解石主要包括四个种类:纤维方解石,交代方解石,晶体方解石和疏松方解石。方解石纤维在78至128 oC的温度下析出,其δ13C签名为-4.91至-7.88‰(VPDB),而δ18O签名为-9.36至-17.34‰(VPDB)。这些方解石是在高温下,低盐度的Na-Cl流体中形成的,该流体可能是源自流星流体或海水的热水混合而成。交代方解石沉淀在62.1至90.0 oC处,δ13C签名为-4.64至-8.59‰(VPDB),δ18O签名为-11.98至-15.08‰(VPDB)。这些流体温度升高,盐度更高,并且钙-Na-Cl组成类似于沉积盆地盐水。根据流体包裹体分析和结果将方解石晶体分为三组,即(a)高温(67至113 oC)低盐度方解石(低于15.14 wt。%),(b)高温(73.7至91.7 oC)高盐度(30至40重量%)方解石,和(c)高温(179.6至199 oC)低盐度(低于7.33 wt。%)方解石。 (a)组的δ13C同位素签名为-5.61至-10.42‰(VPDB)和δ18O签名为-8.35至-16.04‰(VPDB),(b)组的δ13C同位素签名为-4.64至-8.60‰ (VPDB)的δ18O签名为-12.34至-15.04‰(VPDB),(c)组的δ13C签名为-5.59至-8.06‰(VPDB)和δ18O签名为-10.03至-16.17‰(VPDB) 。 (a)组最有可能是由起源于水的热液形成的,(b)组可能是在与蒸发的海水或盆地盐水混合的热液过程中形成的,(c)组似乎是由于陨石和低盐度变质或结晶岩流体的混合物。孔状方解石在85至89 oC析出,其δ13C签名为-7.47至-9.04‰(VPDB),而δ18O签名为-9.32至-10.59‰(VPDB)。这种情况来自高温,高Ca-Na-Cl盐度流体,该流体是与盆地盐水混合的热液。锶同位素比率,th铀比率和与裂缝方解石有关的REE数据表明,它们与主体基岩的水/岩相互作用有限。 specific或铀的某些浓度升高是由于特定岩石类型引起的,例如现场的伟晶岩侵入。

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    Tian Long;

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  • 年度 2016
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