Résumé
The origin of water flowing in faults and fractures at great depth is poorly known in crystalline media. This paper describes a field study designed to characterize the geochemical compartmentalization of a deep aquifer system constituted by a graben structure where a permeable fault zone was identified. Analyses of the major chemical elements, trace elements, dissolved gases and stable water isotopes reveal the origin of dissolved components for each permeable domain and provide information on various water sources involved during different seasonal regimes. The geochemical response induced by performing a pumping test in the fault-zone is examined, in order to quantify mixing processes and contribution of different permeable domains to the flow. Reactive processes enhanced by the pumped fluxes are also identified and discussed. The fault zone presents different geochemical responses related to changes in hydraulic regime. They are interpreted as different water sources related to various permeable structures within the aquifer. During the low water regime, results suggest mixing of recent water with a clear contribution of older water of inter-glacial origin (recharge temperature around 7 degrees C), suggesting the involvement of water trapped in a local low-permeability matrix domain or the contribution of large scale circulation loops. During the high water level period, due to inversion of the hydraulic gradient between the major permeable fault zone and its surrounding domains, modern water predominantly flows down to the deep bedrock and ensures recharge at a local scale within the graben. Pumping in a permeable fault zone induces hydraulic connections with storage-reservoirs. The overlaid regolith domain ensures part of the flow rate for long term pumping (around 20% in the present case). During late-time pumping, orthogonal fluxes coming from the fractured domains surrounding the major fault zone are dominant. Storage in the connected fracture network within the graben structure mainly ensures the main part of the flow rate (80% in the present case). Reactive processes are induced by mixing of water from different sources and transfer conditions. A specific approach is applied to quantify the reaction rate involved along the pumping time. Autotrophic denitrification coupled with iron minerals oxidation is highlighted and water rock interaction is clearly enhanced by the flux changes induced by pumping. Abstract Copyright (2014) Elsevier, B.V.