4.6 Article

Combining stable isotope (2H, 18O, and 87Sr/86Sr) and hydrochemistry to understand hydrogeochemical processes in karst groundwater system, Xin'an, northern China

Journal

ENVIRONMENTAL EARTH SCIENCES
Volume 82, Issue 9, Pages -

Publisher

SPRINGER
DOI: 10.1007/s12665-023-10906-2

Keywords

Karst groundwater; Hydrogeochemical process; Strontium isotope; Water-rock interactions; Principal component analysis

Ask authors/readers for more resources

In this study, multiple hydrogeochemical indices and isotopes were used to analyze the factors controlling groundwater salinization and processes in the Xin'an karst groundwater system in Shanxi, China. The region's karst groundwater system was divided into three subsystems with distinct geological characteristics. The dominant chemical type of the karst groundwater system was HCO3-Ca center dot Mg. Hydrogeochemical processes differed between subsystems, with Sr2+ content and TDS concentrations increasing along the flow direction in two subsystems, while decreasing in the third subsystem. Major ions originated from carbonate and sulfate minerals dissolution, with sulfate minerals dissolution being the main contributor to the increase in groundwater salinity. The results provide valuable insights for the management and utilization of karst groundwater resources.
Karst groundwater is the most important source of water supply for Shanxi province, northern China. In this study, different hydrogeochemical indices along with multiple isotope (H-2, O-18, and Sr-87/Sr-86) were used to identify the main factors controlling groundwater salinization and hydrogeochemical processes in the Xin'an karst groundwater system at Shanxi. The region's karst groundwater system was divided into three geologically distinct subsystems, namely, the Changzhi-Xiangyuan subsystem (C-X), Huguan-Pingshun subsystem (H-P), and Licheng subsystem (LC). HCO3-Ca center dot Mg was dominant chemical type for karst groundwater system. The H-P and LC subsystems experienced similar hydrogeochemical processes; from the recharge zone to discharge zone, the Sr2+ content, Sr2+/Ca2+ ratio, and TDS concentrations of karst groundwater gradually increase along the flow direction. However, for C-X subsystem, from the deep buried zone to discharge zone, the Sr2+ content, Sr2+/Ca2+ ratio, and TDS concentrations gradually decrease due to the mixing of fresh water. The main source of karst groundwater was meteoric water, and it is also recharged by surface water and shallow groundwater. The water-rock interactions in conjunction with the cation exchange absolutely predominated in hydrogeochemical evolution of karst groundwater. Major ions, such as Ca2+, Mg2+, HCO3-, and SO42-, originated from the dissolution of carbonate and sulfate minerals. Dissolution of sulfate minerals was the major process for the increase of groundwater salinity. The NO3-, Cl-, and K+ could be attributed to agricultural and human activities, and the Na+ originated from intense mining activities in the study area. The results will facilitate understanding of hydrogeochemical processes and groundwater pollution to enable effective management and utilization of karst groundwater resources.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available