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Hydrogeochemistry, groundwater ages and sources of salts in a granitic batholith on the Canadian Shield, southeastern Manitoba

机译:马尼托巴东南部加拿大盾构的花岗岩基岩中的水文地球化学,地下水年龄和盐分来源

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The hydrogeochemistry of the Lac du Bonnet granitic batholith has been determined for the region of the Whiteshell Research Area (WRA) in southeastern Manitoba, Canada. This work forms part of the geosciences studies performed for the Canadian Nuclear Fuel Waste Management Program over the period 1980-1995 by Atomic Energy of Canada Limited (AECL). Knowledge of the variation of groundwater chemistry and its causes is useful in assessing the performance and safety of a nuclear fuel waste vault located at depths of up to 1000 m in a crystalline rock formation of the Canadian Shield. Groundwaters and matrix pore fluids have been obtained by standard sampling methods from shallow piezometers in clay-rich overburden, from packer-isolated borehole zones intersecting fractures or fault zones in the bedrock, and from boreholes in unfractured rock in AECL's Underground Research Laboratory (URL). Eighty-six individual fracture groundwaters have been sampled and analysed from permeable zones in 53 boreholes drilled to depths of up to 1000 m in the Lac du Bonnet batholith. In addition, 28 groundwaters from piezometers in a large wetland area near the URL have been sampled and analysed to determine the influence of clay-rich overburden on the bedrock hydrogeochemistry. Analyses have been made for major and minor ions, pH, Eh, trace metals, and stable and radioactive isotopes, to characterise these groundwaters and relate them to their hydrogeologic regimes. Shallow groundwaters in the fractured bedrock are generally dilute (TDS <0.3 g/l), Ca-Na-HCO3 waters and show little indication of mixing with Ca-Mg-HCO3-SO4 groundwater from overburden sediments. The near-modern levels of 3 H and C-14, and a warm-climate H-2/O-18 signature in these groundwaters, indicates that the upper similar to200 m of fractured bedrock contains an active groundwater circulation system with a residence time of tens to hundreds of years. Deeper fracture groundwaters (200-400 m depth) in recharge areas, are more alkaline, Na-Ca-HCO3 waters and evolve to Na-Ca-HCO3-O-SO4 waters with increasing distance along the flow path. Isotopic data indicate the presence of a glacial melt-water component suggesting that the residence times of these waters are 10(3)-10(5) a. These waters form a transition zone between the upper, advective flow regime and a deeper regime in sparsely fractured rock where groundwater in fractures and fracture zones is largely stagnant. At these depths (> 500 m), Na-Ca-Cl-SO4 waters of increasing salinity (up to 50 g/l) with depth are found and in some fractures the waters have evolved to a Ca-Na-Cl composition. Isotopic data indicate that these waters are warm-climate and pre-glacial in origin, with residence times of over 1 Ma. Pore fluids observed to drain from the unfractured rock matrix in the URL facility are almost pure Ca-Cl in composition, similar to90 g/l salinity, and have a H-2/O-18 composition displaced well to the left of the global meteoric water line, about which all other WRA groundwaters lie. This information indicates that these pore fluids have undergone prolonged water-rock interaction and have residence times of 10(1-)10(3) Ma. Most of the deeper fracture groundwaters and pore fluids have low Br/Cl ratios and moderate to high delta(34)S values of dissolved SO4 which indicates that their salinity could be derived from a marine source such as the basinal sedimentary brines and evaporites to the west of the batholith. These fluids may have entered the batholith during early Palcozoic times when sedimentary rocks were deposited over the granite and were driven by a hydraulic gradient resulting from higher ground in western Canada. The hydrogeochemical data and interpretations show that below similar to500 m in the WRA, fracture-hosted groundwaters are very saline, reducing and old, and are, therefore, indicative of stagnant conditions over the period of concern for nuclear waste disposal (1 Ma). The intact rock matrix at these depths i
机译:已经确定了加拿大东南部曼尼托巴省怀特贝研究区(WRA)地区的Lac du Bonnet花岗岩基岩的水文地球化学。这项工作是加拿大原子能有限公司(AECL)在1980-1995年间为加拿大核燃料废物管理计划进行的地球科学研究的一部分。了解地下水化学变化及其成因有助于评估位于加拿大盾构结晶岩层中深达1000 m的核燃料废物库的性能和安全性。地下水和基质孔隙流体是通过标准采样方法从富粘土覆盖层中的浅压计,与岩层中裂缝或断层带相交的与封隔器隔离的钻孔区域以及AECL地下研究实验室(URL)的未破裂岩石的钻孔中获得的。在Lac du Bonnet基岩中,从53个钻孔中的渗透性区域采样了86个单独的裂缝性地下水,并进行了分析,钻孔深度达1000 m。此外,对URL附近一个大湿地中的压力计中的28个地下水进行了采样和分析,以确定富含粘土的覆盖层对基岩水文地球化学的影响。已对主要和次要离子,pH,Eh,痕量金属以及稳定和放射性同位素进行了分析,以表征这些地下水并将其与水文地质状况联系起来。裂隙基岩中的浅层地下水通常是稀水(TDS <0.3 g / l),Ca-Na-HCO3水,几乎没有迹象表明与上覆沉积物中的Ca-Mg-HCO3-SO4地下水混合。这些地下水中3 H和C-14的水平接近现代水平,并具有温暖气候的H-2 / O-18特征,这表明与200 m裂缝基岩相似的上部包含一个活跃的地下水循环系统,其停留时间为几十到数百年。补给区中较深的裂缝性地下水(深度为200-400 m)是碱性更强的Na-Ca-HCO3水,并随着沿流径的距离的增加而演化为Na-Ca-HCO3-O-SO4水。同位素数据表明存在冰川融化水成分,表明这些水的停留时间为10(3)-10(5)a。这些水在稀疏裂隙岩石中形成较高的对流流动状态和较深状态之间的过渡区域,在该区域中,裂隙和裂隙区域中的地下水大部分处于停滞状态。在这些深度(> 500 m)处,发现了随着深度增加盐度(高达50 g / l)的Na-Ca-Cl-SO4水,并且在某些裂缝中,水已演化为Ca-Na-Cl成分。同位素数据表明,这些水源是温暖气候和冰期前的,停留时间超过1 Ma。在URL设施中观察到从未破裂的岩石基质中排出的孔隙液的成分几乎是纯Ca-Cl,类似于90 g / l的盐度,并且H-2 / O-18成分很好地排到了全球陨石的左侧WRA所有其他地下水所在的水线。该信息表明,这些孔隙流体经历了长时间的水-岩相互作用,并且停留时间为10(1-)10(3)Ma。大多数较深的裂缝性地下水和孔隙流体的Br / Cl比率低,溶解的SO4的中值(34)S值较高,这表明其盐度可能来自海洋来源,如盆地沉积盐水和蒸发岩。基岩以西。这些流体可能是在古生代初期进入沉积岩层的,当时沉积岩沉积在花岗岩上,并且受加拿大西部高地的水力梯度驱动。水文地球化学数据和解释表明,在WRA中,类似于500 m以下,裂缝带动的地下水含盐量高,减少且陈旧,因此表明在核废料处置期间(1 Ma)停滞不前。在这些深度下完整的岩石矩阵

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