Artificial recharge of groundwater is often used to either purify partially treated wastewater or to enhance the quality of surface water by percolation through a variably saturated zone. In many cases, the most substantial purification process within the infiltration water is the redox-dependent biodegradation of organic substances. The present study was aimed at understanding the spatial and temporal distribution of the redox reactions that develop below an artificial recharge pond near Lake Tegel, Germany. At this site, like at many artificial recharge sites, the hydraulic regime immediately below the pond is characterised by cyclic changes between saturated and unsaturated conditions. These changes, which occur during each operational cycle, result from the repeated formation of a clogging layer at the pond bottom. Regular hydrogeochemical analyses of groundwater and seepage water in combination with continuous hydraulic measurements indicate that NO3 - and Mn-reducing conditions dominate beneath the pond as long as water-saturated conditions prevail. Manganese-, Fe- and SO24 -reducing conditions are confined to a narrow zone directly below the clogging layer and in zones of lower hydraulic conductivity. The formation of the clogging layer leads to a steady decrease of the infiltration rate, which ultimatively causes a shift to unsaturated conditions below the clogging layer. Atmospheric O2 then starts to penetrate from the pond fringes into this region, leading to: (i) the re-oxidation of the previously formed sulphide minerals and (ii) the enhanced mineralisation of sedimentary particulate organic C. The mineralisation of sedimentary particulate organic C leads to an increased H2CO3 production and subsequent dissolution of calcite.

A modelling study was carried out to provide a process-based quantitative interpretation of the biogeochemical changes that were observed during an ASR experiment in which reclaimed water was injected into a limestone aquifer at a field-site near Bolivar, South Australia. A site-specific conceptual model for the interacting hydrodynamic and biogeochemical processes that occur during reclaimed water ASR was developed and incorporated into an existing reactive multi-component transport model. The major reactive processes considered in the model were microbially mediated redox reactions, driven by the mineralisation of organic carbon, mineral precipitation/ dissolution and ion exchange. The study showed that the geochemical changes observed in the vicinity of the ASR well could only be adequately described by a model that explicitly considers microbial growth and decay processes, while an alternative, simpler model formulation based on the assumption of steady state biomass concentration failed to reproduce the observed hydrochemical changes. However, both, the simpler and the more complex model approach were able to reproduce the geochemical changes further away from the injection/extraction well. These changes were interpretated as a result of the combined effect of ion exchange, calcite dissolution and mineralisation of dissolved organic carbon.

Managed aquifer recharge is an increasingly popular technique to secure and enhance water supplies. Among a range of recharging techniques, single-well aquifer storage and recovery (ASR) is becoming a common option to either augment drinking water supplies or facilitate reuse of reclaimed water. For the present study a conceptual biogeochemical model for reclaimed water ASR was developed and incorporated into an existing reactive multicomponent transport model. The conceptual and numerical model for carbon cycling includes various forms of organic and inorganic carbon and several reactive processes that transfer carbon within and across different phases. The major geochemical processes considered in the model were microbially mediated redox reactions, driven by the mineralization of organic carbon, mineral dissolution/ precipitation, and ion exchange. The numerical model was tested and applied for the analysis of observed data collected during an ASR field experiment at Bolivar, South Australia. The model simulation of this experiment provides a consistent interpretation of the observed hydrochemical changes. The results suggest that during the storage phase, dynamic changes in bacterial mass have a significant influence on the local geochemistry in the vicinity of the injection/extraction well. Farther away from the injection/extraction well, breakthrough of cations is shown to be strongly affected by exchange reactions and, in the case of calcium, by calcite dissolution.

In Berlin, 70 % of the drinkinq water is derived from bank filtrate or artificially recharged water. Because the surface water system contains elevated proportions of secondary treated municipal sewage, a number of sewage indicators from various sources can be detected in the bank filtrate. An artificial recharge site and a bank filtration site in Berlin Tegel are introduced and compared in terms of their hydrogeological and hydrochemical properties. Because of a permanent clogging layer and the geological properties, travel times are slower at the BF site and the hydrochemical conditions are more reducing. First estimates for the reaction rate constants of oxygen and nitrate are obtained with exponential data fitting. Some of the effects of the different redox conditions on minor substances such as drug residues are highlighted.

The present report characterizes the field sites Lake Tegel and Lake Wannsee as well as the artificial recharge site GWA Tegel in terms of their clogging layer, sedimentary, hydraulic and hydrochemical properties. As a result, a solid basis for the interpretation of specific compounds evaluated within NASRI and for subsequent modeling and quantification of the data is given. Major problems or difficulties where identified, in order to focus investigations on aspects not fully understood to date in the next project phase. The combination of different tracers enables the interpretation of the flow regime. With the help of T/He analysis, ages of different water bodies can be estimated. The analysis of tracer showing distinct seasonal variations is used to estimate travel times while water constituents which are either mainly present in the bank filtrate or the background water are used for mixing calculations. The proportions of treated wastewater in the surface water were estimated in front of the transects. The surface water composition varies largely both in time and space, which is a problem at Wannsee, where the surface water sampling point is not representative for the bank filtration input. Estimates for travel times of the bank filtrate to individual observation and production wells are given and vary between days and several months. The production wells are a mixture of bank filtrate and water from inland of the wells and deeper aquifers, proportions of bank filtrate are given where possible to differentiate between contaminant removal and dilution. They vary between < 20 and > 80 %. The new observation wells enable a vertical differentiation of the infiltrate. It becomes clear that at Tegel and Wannsee, there is a strong vertical succession towards larger proportions of considerably older bank filtrate with depth. At the Wannsee transect, the observation wells deeper than the lake do not reflect the surface water signal at all. It will be important to combine the new information with hydraulic information of existing flow models (mainly of the IGB “model” group). The evaluation of the redox conditions shows that redox successions proceed with depth rather than (only) in flow direction. In addition, the redox zoning (as characterised by the appearance or disappearance of redox sensitive species) is very transient. The zones are much wider in winter than in summer, in particular at the artificial recharge site GWA Tegel, probably due to temperature effects. This poses a challenge for the desired modelling and the interpretation of data from redoxsensitive substances.