首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >An evaporated seawater origin for the ore-forming brines in unconformity-related uranium deposits (Athabasca Basin, Canada): Cl/Br and δ~(37)Cl analysis of fluid inclusions
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An evaporated seawater origin for the ore-forming brines in unconformity-related uranium deposits (Athabasca Basin, Canada): Cl/Br and δ~(37)Cl analysis of fluid inclusions

机译:与不整合有关的铀矿床中的成矿盐水的蒸发海水成因(加拿大阿萨巴斯卡盆地):流体包裹体的Cl / Br和δ〜(37)Cl分析

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Analyses of halogen concentration and stable chlorine isotope composition of fluid inclusions from hydrothermal quartz and carbonate veins spatially and temporally associated with giant unconformity-related uranium deposits from the Paleoproterozoic Athabasca Basin (Canada) were performed in order to determine the origin of chloride in the ore-forming brines. Microthermometric analyses show that samples contain variable amounts of a NaCl-rich brine (Cl concentration between 120,000 and 180,000ppm) and a CaCl_2-rich brine (Cl concentration between 160,000 and 220,000ppm). Molar Cl/Br ratios of fluid inclusion leachates range from ~100 to ~900, with most values between 150 and 350. Cl/Br ratios below 650 (seawater value) indicate that the high salinities were acquired by evaporation of seawater. Most δ~(37)Cl values are between -0.6‰ and 0‰ (seawater value) which is also compatible with a common evaporated seawater origin for both NaCl- and CaCl_2-rich brines.Slight discrepancies between the Cl concentration, Cl/Br, δ~(37)Cl data and seawater evaporation trends, indicate that the evaporated seawater underwent secondary minor modification of its composition by: (i) mixing with a minor amount of halite-dissolution brine or re-equilibration with halite during burial; (ii) dilution in a maximum of 30% of connate and/or formation waters during its migration towards the base of the Athabasca sandstones; (iii) leaching of chloride from biotites within basement rocks and (iv) water loss by hydration reactions in alteration haloes linked to uranium deposition.The chloride in uranium ore-forming brines of the Athabasca Basin has an unambiguous dominantly marine origin and has required large-scale seawater evaporation and evaporite deposition. Although the direct evidence for evaporative environments in the Athabasca Basin are lacking due to the erosion of ~80% of the sedimentary pile, Cl/Br ratios and δ37Cl values of brines have behaved conservatively at the basin scale and throughout basin history.
机译:为了确定矿石中氯化物的来源,对时空与时间上与古元古代阿萨巴斯卡盆地(加拿大)不整合相关的铀矿床有关的热液石英和碳酸盐脉状流体包裹体中的卤素浓度和稳定的氯同位素组成进行了分析。形成盐水。微量热分析表明,样品中含有可变数量的富NaCl盐水(Cl浓度在120,000至180,000ppm之间)和富CaCl_2盐水(Cl浓度在160,000至220,000ppm之间)。流体包裹渗滤液的摩尔Cl / Br比在〜100至〜900范围内,大多数值在150至350之间。Cl/ Br比低于650(海水值)表明高盐度是通过蒸发海水获得的。对于富含NaCl和CaCl_2的盐水,大多数δ〜(37)Cl值都在-0.6‰至0‰(海水值)之间,这也与常见的蒸发海水来源相容.Cl浓度,Cl / Br之间的微小差异δ〜(37)Cl数据和海水蒸发趋势表明,蒸发的海水通过以下方式进行了次要的次要改变:(i)在埋葬期间与少量的盐酸盐溶解盐水混合或与盐酸盐重新平衡; (ii)在向阿萨巴斯卡砂岩底部迁移的过程中,最多稀释30%的原生水和/或地层水; (iii)从基底岩中的黑云母中浸出氯化物,以及(iv)与铀沉积有关的蚀变晕中由于水合反应而发生水合作用而失水。阿萨巴斯卡盆地铀矿形成盐水中的氯化物具有明确的主要海洋成因,并且需要大量大规模海水蒸发和蒸发物沉积。尽管由于〜80%的沉积堆被侵蚀而缺乏阿萨巴斯卡盆地蒸发环境的直接证据,但在盆地规模和整个盆地历史上,盐水的Cl / Br比和δ37Cl值都表现出保守性。

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