...
首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Monitoring and reactive-transport modeling of the spatial and temporal variations of the Strengbach spring hydrochemistry
【24h】

Monitoring and reactive-transport modeling of the spatial and temporal variations of the Strengbach spring hydrochemistry

机译:Strengbach春季水化空间和时间变化的监测与反应运输建模

获取原文
获取原文并翻译 | 示例

摘要

This study focuses on 20 years of hydrochemical monitoring of the small springs that emerge in the experimental granitic catchment of Strengbach (OHGE, France) and the simulation of these data using the KIRMAT code. The data indicate that the Strengbach springs display chemostatic behavior; that is, limited temporal variations were noted in the concentrations of dissolved silica (H4SiO4) and most of the basic cations during the studied period (1987-2010), resulting in relative stability of the global weathering fluxes exported by the springs. Only the Ca2+ concentrations reflect a significant decrease in all the Strengbach springs since 1987, and the variations differ from one spring to another. The modeling results show that the decrease in Ca2+ in the Strengbach springs is due to the response of the water-rock interactions within the bedrock to the variations in the chemical composition of the soil solutions, which were characterized by a significant increase in pH and a decrease in Ca2+ concentrations between 1987 and 2010. The decrease in Ca2+ concentrations seen in the Strengbach springs is controlled by changes in the apatite dissolution rate and the compositions of clay minerals induced by the soil solution changes. The differences observed between the Ca2+ trends of the springs are related to changes in the residence time of the water supplying the different springs. The weak impact of the soil solution modifications on the dissolution rates of other primary minerals and on the bulk precipitation rates of the clay minerals explains the relative stability over time of the concentrations of the other cations and dissolved silica in the water derived from the Strengbach springs. Further, the hydrochemical simulations suggest that the chemostatic behavior of the Strengbach springs cannot be explained by the mobilization of waters that are close to chemical equilibrium, but rather by a hydrological control of the spring water residence times. Finally, a compariso
机译:本研究侧重于20年的小泉水监测,在Strengbach(OHGE,法国)的实验性削减中出现的小型泉水和使用Kirmat代码的模拟这些数据的模拟。数据表明Strengbach Springs显示出化学行为;即,在溶解二氧化硅(H4SIO4)的浓度下,在研究期间(1987-2010)期间,在溶解二氧化硅(H4SIO4)和大部分基本阳离子的浓度下,导致由弹簧出口的全球风化助熔剂的相对稳定性。只有1987年以来,只有CA2 +浓度反映了所有Strengbach弹簧的显着降低,并且变化与一个弹簧不同。建模结果表明,Strengbach弹簧中的CA2 +降低是由于岩石内的水岩相互作用对土壤溶液化学成分的变化的响应,其特征在于pH和a的显着增加1987年至2010年之间的Ca2 +浓度降低。在Strentbach弹簧中看到的Ca2 +浓度的降低由磷灰石溶出速率的变化和土壤溶液诱导的粘土矿物质的组成进行控制。弹簧的CA2 +趋势之间观察到的差异与供应不同弹簧的水的停留时间的变化有关。土壤溶液改性对其他初级矿物质溶出速率的弱势和对粘土矿物的块状沉淀速率的影响解释了其他阳离子浓度随时间的相对稳定性,并在来自Strengbach弹簧的水中的水中的溶解二氧化硅随着时间的推移。此外,水化学模拟表明Strengbach弹簧的化疗行为不能通过靠近化学平衡的水,而是通过弹簧水停留时间的水文控制来解释。最后,比较

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号