Depth–Sequential Investigation of Major Ions, δ18O, δ2H and δ13C in Fractured Aquifers of the St. Lawrence Lowlands (Quebec, Canada) Using Passive Samplers

Abstract

General and isotopic geochemistry of groundwater is an essential tool to decipher hydrogeological contexts and flow paths. Different hydrogeochemical patterns may result from the inherent physical aquifer heterogeneity, which may go unnoticed without detailed investigations gathered from multilevel or multiple observation wells. An alternative to overcome the frequent unavailability of multiple wellbores at sites is to perform a detailed investigation on the single wellbore available. In this perspective, the aim of this study is to use passive samplers to sequentially collect groundwater at depths in long–screened wellbores. Such investigation is carried out for major ions and stable isotopes compositions (δ2H, δ18O, δ13C) at ten sites in the context of fractured carbonate aquifers of the St. Lawrence Lowlands (Quebec, Canada). The information gathered from the calco–carbonic system, major ions and stable isotopes report poorly stratified and evolved groundwater bodies. Contribution of water impacted by anthropogenic activities, such as road salts pollution and carbon sources from C4 vegetation, when they occur, are even observed at the greatest depths. Such observations suggest quick flow paths and efficient mixing conditions, which leads to significant contributions of contemporary groundwater bodies in the fractured aquifers investigated down to depths of about 100 m. Although physical aquifer investigation reported few and heterogeneously distributed fractures per wellbore, hydrogeochemical findings point to at overall well interconnected fracture networks in the aquifer and high vulnerability of groundwater, even at significant depths.