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利用稳定同位素和乙酰磺胺酸钾定量地表水/地下水界面的长期废水通量:综合模型视角

Quantification of long-term wastewater fluxes at the surface water/groundwater-interface: an integrative model perspective using stable isotopes and acesulfame.

机构信息

Forschungszentrum Jülich, Institute of Bio- and Geosciences, Agrosphere - IBG-3, Germany; Technical University of Darmstadt, Institute of Applied Geosciences, Germany.

出版信息

Sci Total Environ. 2014 Jan 1;466-467:16-25. doi: 10.1016/j.scitotenv.2013.06.092. Epub 2013 Jul 25.

Abstract

The suitability of acesulfame to trace wastewater-related surface water fluxes from streams into the hyporheic and riparian zones over long-term periods was investigated. The transport behavior of acesulfame was compared with the transport of water stable isotopes (δ(18)O or δ(2)H). A calibrated model based on a joint inversion of temperature, acesulfame, and piezometric pressure heads was employed in a model validation using data sets of acesulfame and water stable isotopes collected over 5months in a stream and groundwater. The spatial distribution of fresh water within the groundwater resulting from surface water infiltration was estimated by computing groundwater ages and compared with the predicted acesulfame plume obtained after 153day simulation time. Both, surface water ratios calculated with a mixing equation from water stable isotopes and simulated acesulfame mass fluxes, were investigated for their ability to estimate the contribution of wastewater-related surface water inflow within groundwater. The results of this study point to limitations for the application of acesulfame to trace surface water-groundwater interactions properly. Acesulfame completely missed the wastewater-related surface water volumes that still remained in the hyporheic zone under stream-gaining conditions. In contrast, under stream-losing conditions, which developed after periods of stagnating hydraulic exchange, acesulfame based predictions lead to an overestimation of the surface water volume of up to 25% in the riparian zone. If slow seepage velocities prevail a proportion of acesulfame might be stored in smaller pores, while when released under fast flowing water conditions it will travel further downstream with the groundwater flow direction. Therefore, under such conditions acesulfame can be a less-ideal tracer in the hyporheic and riparian zones and additional monitoring with other environmental tracers such as water stable isotopes is highly recommended.

摘要

研究了醋磺胺钾作为示踪剂,追踪来自溪流的废水相关地表水通量,在长时间内进入潜流带和河岸带的适用性。比较了醋磺胺钾的传输行为与水稳定同位素(δ(18)O 或 δ(2)H)的传输行为。在一个溪流和地下水的 5 个月数据集中,使用基于温度、醋磺胺钾和测压水头联合反演的校准模型对模型进行了验证。通过计算地下水年龄来估计地表水入渗引起的地下水中淡水的空间分布,并将其与经过 153 天模拟时间后获得的预测醋磺胺钾羽流进行比较。研究了利用水稳定同位素混合方程计算的地表水比和模拟的醋磺胺钾质量通量,以确定它们估算地下水中废水相关地表水流入量的能力。本研究的结果表明,醋磺胺钾在正确追踪地表水-地下水相互作用方面存在局限性。在溪流增益条件下,醋磺胺钾完全错过了仍滞留在潜流带中的废水相关地表水体积。相比之下,在停滞水力交换后发展的溪流损耗条件下,基于醋磺胺钾的预测会导致河岸带中地表水体积高估高达 25%。如果缓慢的渗流速度占主导地位,一部分醋磺胺钾可能会储存在较小的孔隙中,而当在快速流动的水条件下释放时,它会沿着地下水流动方向向下游移动更远。因此,在这种情况下,醋磺胺钾在潜流带和河岸带中可能不是一个理想的示踪剂,强烈建议使用其他环境示踪剂(如水稳定同位素)进行额外监测。

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