Groundwater pollution | EPFL Graph Search

Groundwater pollution (also called groundwater contamination) occurs when pollutants are released to the ground and make their way into groundwater. This type of water pollution can also occur naturally due to the presence of a minor and unwanted constituent, contaminant, or impurity in the groundwater, in which case it is more likely referred to as contamination rather than pollution. Groundwater pollution can occur from on-site sanitation systems, landfill leachate, effluent from wastewater treatment plants, leaking sewers, petrol filling stations, hydraulic fracturing (fracking) or from over application of fertilizers in agriculture. Pollution (or contamination) can also occur from naturally occurring contaminants, such as arsenic or fluoride. Using polluted groundwater causes hazards to public health through poisoning or the spread of disease (water-borne diseases). The pollutant often creates a contaminant plume within an aquifer. Movement of water and dispersion within the aquif

Study of the microbial communities of core and water samples in a chloroethenes contaminated aquifer

Guillaume Laulan

Widely used in industrial activities, chloroethenes have become common groundwater contaminants. Dehalorespiration is an anaerobic bacterial respiration coupling their sequential degradation to energy production. The interactions between the dehalorespiring bacteria and the other guilds and environmental variables are presumed to influence the dehalorespiration efficiency. Here, water and core samples were extracted from the PCE-contaminated site of Lyss (BE, Switzerland). Bacterial DNA was extracted and the 16S rRNA gene amplified by PCR. Terminal restriction fragment length polymorphism (T-RFLP) was used to assess the diversity of the bacterial communities. Core and groundwater environmental variables were analyzed as well. The T-RFLP profiles and the environmental data obtained were processed using statistical multivariate analysis. Within a period of two months, the bacterial communities remained relatively specific to their respective sampling origins. Communities from the oxic layer shared a similar set of bacterial species whereas piezometers from the anoxic layer had a specific one. The T-RFLP profiles obtained from single depth and multi-level piezometers were clearly distinct, probably due to differences in the pumping flow rates and their associated transport regimes, which can have an impact on i) the sediments extracted from the aquifer, ii) the hydraulic zone reached and iii) a potential selective bacterial adsorption onto the pumping tube wall. Environmental factors related to the groundwater redox state appeared as the major variables influencing the bacterial populations. Bacterial communities from core samples clustered into two distinct sets: i) samples from the strongly reductive silt layer, and ii) samples from the coarser and less reductive layer. Grain size distribution and redox state both had a major influence on the bacterial communities of core samples. Finally, it was shown that microbial populations extracted from groundwater differed from the ones extracted from core material, and thus were not representative of the overall aquifer microbial diversity.

2009

Fonctionnement et gestion des aquifères alluviaux de haute altitude

The Haute Sarine alpine valley is located at an average altitude of approximately 1'000 to 1'200 masl. It was formed in its southern part up to the area of Gstaad to the favour of a typical North-South tectonic fault according to the main structures of the Préalpes, then followed normal fault striking East-West to end up on the rock bolt of the Vanel hill. The late and postglacial period was marked by the deposition of glaciolacustrines, glaciofluviatile and flurecent fluviatile sediments which have filled the ice free valley bottom probably starting from a period older than the Bölling-Alleröd interstadial. The depth of this overdeepening varies between 20 and more than 50 m of depth. Drillings which we carried out could document series of typical glaciolacustrine sediments. The implementation of several geophysical survey methods (resistivity, seismic refraction and reflexion, well logs and pumping tests) enabled us to analyse several sources of information which we confronted between them in order to produce a 3D model of the quaternary deposits and their hydrological properties. Most of these sediments are relatively quite permeable and build a free groundwater reservoir that we subdivided into 3 parts. The basin of Gsteig in the south is closed, the valley having been blocked by a massive landslide that probably occurred in several successive stages starting at the first climate improvements. The second part, the basin of Feutersoey has not been retained as a potential important hydrogeologic resource based on our preliminary investigations. The last basin, that of Gstaad-Saanen is the largest and thickest. It is also in this basin that most of the tourist and industrial activities of the area are concentrated. The observation network was established in order to characterize the groundwater flows enabling us at the same time to carry out piezometric measurements and chemical as well as and bacteriological analyses. We also carried out a δ18O isotope analysis campaign. The whole of these approaches highlighted the particular characteristics of the groundwater recharge. The groundwater system is mainly fed by the Sarine and the precipitations infiltration. We also located an underground karstic feeding of evaporitic type. We finally propose a groundwater management and protection concept adapted to the particular situation of the Sarine alluvial mountain aquifer system on both quantitative and qualitative aspects. The high altitude alpine groundwater catchment areas such as the Haute Sarine represent as a whole a quality resource, with high potentials yet to be defined on a larger scale, for example by applying numerical modeling and by organizing and maintaining long term observation networks that will enable us to define a sustainable groundwater resource management within the alpine area.

EPFL2000

Typology of recent groundwaters from different aquifer environments based on geogenic tracer elements

A key problem in environmental science and in engineering geology is the often incomplete understanding of the origin of dissolved components in groundwater. The dissolved contents of trace elements in groundwater are of special importance for groundwater quality control. The AQUITYP project aims to establish a detailed typology of recent groundwaters based on their geogenic trace element compositions, and to derive a so-called "geo-reference" for groundwaters from five principal aquifer lithologies in the Alpine belt. This geo-reference provides a database for investigations related to groundwater contamination, groundwater resources management and engineering geology. Groundwaters from crystalline, carbonate, and evaporite rocks, as well as molasse and flysch sediments in Switzerland and in neighbouring countries were sampled and documented by previous researchers (Dubois, 1993; Dematteis, 1995; Mandia, 1993; Hesske, 1995; Basabe, 1993). Based on a statistical analysis of the data and examination of the relationship between aquifer lithology and chemical groundwater composition these researchers identified a number of characteristic tracer elements (geogenic tracers). The present study includes (1) a synthesis of the hydrogeology and the hydrochemistry of recent groundwaters in these five aquifer types based on groundwater data acquired within the AQUITYP project, and (2) a hydro-geochemical investigation of the origin and chemical behaviour of the geogenic tracer chromium, based on a comprehensive field and laboratory study. To enable a comparison of the chemical groundwater data gathered and analysed over a time span of 20 years, a rigorous quality control of the entire database was made. An assessment was made of the sampling techniques, the sample treatment and the analytical methods applied in the AQUITYP project since 1981. Different tests were carried out to evaluate the quality and comparability of the data, including geochemical model calculations, comparison of different analytical techniques, and tests to estimate the influence of the filtration procedure. In order to make this large number of quality controlled data accessible also for future investigations, a groundwater data storage system was developed (AQUITYP-DataBase). 1.) Typology of recent groundwaters In the synthesis of groundwater hydrochemistry, the emphasis was laid on the hydro-geochemical evolution leading to the characteristic groundwater composition in each of the five aquifer types. Chemical characteristics and differences between the groundwaters from the different aquifer types were identified and natural concentration ranges for each aquifer type derived. The proposed geogenic tracers were evaluated and the potential sources of these tracers identified. The dominant processes leading to the typical mineralisation of recent groundwaters were investigated using geochemical modelling strategies. Finally, the concentrations of chemical elements in the groundwaters from the different aquifer types were compared to the Swiss drinking water standards in order to assess the quality of the investigated groundwaters. It has been found that each rock type contributes in a characteristic way to the major and trace element composition of the corresponding groundwater: The groundwaters derived from the crystalline Mont-Blanc and Aiguilles-Rouges massifs are characterised by a low total mineralisation (TDS 22 to 158 mg/L) dominated by Ca2+, Na+, Mg2+, alkalinity, SO42-, and F- (Ca-Na-HCO3,-SO4, waters). Elevated amounts of Mo, U, W, and As occur. These groundwaters derive their mineralisation mainly from the interaction with hydrothermal minerals present along fractures. Fractures act as major groundwater flow paths. Minerals relevant for groundwater mineralisation include carbonates (Ca2+, Mg2+, HCO3-), clay minerals (Ca-Na ion exchange), fluorite (F-, Ca2+), Fe-, As-, and Mo-sulphides (SO42-, As, Mo), and U- and W-minerals (U, W). In these crystalline groundwaters the natural concentrations of F- (23% of the investigated springs) and As (7%) exceed the Swiss limits for drinking water. In addition, the WHO guideline values for U are exceeded in 65% of the cases and for Mo in 15% of the cases. The carbonate karst groundwaters obtain their low to intermediate mineralisation (TDS 161 to 547 mg/L) from the dissolution of calcite (Ca-HCO3, waters), as well as in certain regions dolomite (Ca-Mg-HCO3, waters) and gypsum (Ca-Mg-HCO3,-SO4, waters). Together with their very short residence times, the carbonate karst groundwaters generally contain very low trace element contents. Nevertheless, geogenic trace elements occur in specific regions in relation with fossil organic matter (I, V) and accessory minerals such as barite in deep sea limestones (Ba), evaporite minerals (gypsum, celestite: Sr, Li), clay- and Fe-minerals (V), and Mo-sulphides and U-minerals in dolomitic limestones (Mo, U). In 18% of the carbonate karst springs atmospheric derived Pb exceeds the Swiss drinking water quality target value. The groundwaters from Triassic evaporites in the Swiss Rhone basin are characterised by a high total mineralisation (TDS 760 to 2788 mg/L) expressed by elevated amounts of Ca2+, Mg2+, Sr2+, SO42-, and alkalinity (Ca-Mg-SO4-HCO3 waters). Elevated amounts of the trace elements Mn, Ni, Cu, Li, Rb, Y, and Cd occur. The hydrochemical evolution of these groundwaters is governed by incipient dedolomitisation, involving dissolution of gypsum, celestite and dolomite and simultaneous precipitation of calcite. The Na+ and K+ contents probably controlled by ion-exchange reactions on clay minerals. Characteristic trace elements originate mainly from the dissolution of dolomite (Mn, Ni) and small amounts of apatite (Y, Cd), and from the oxidation of sulphide minerals (Cu, Ni, Cd). The elevated concentrations of the highly soluble Li and Rb may be related to brine inclusions in evaporite minerals and eventually to clay minerals. These evaporite groundwaters contain SO42- concentrations exceeding the Swiss quality target for drinking water in all springs, and the concentrations of U and Ni exceed the WHO guideline values in respectively 58% and 2% of the cases. In addition, Mn, Cd, and As concentrations exceed the Swiss quality targets in respectively 11%, 10%, and 7% of the investigated springs. Recent groundwaters circulating in the porous and fissured molasse sandstones and conglomerates acquire their intermediate mineralisation (TDS 48 to 714 mg/L) primarily by dissolution of calcite and minor dolomite (Ca-Mg-HCO3 waters). The particular mineralogy of certain Molasse formations is reflected in specific trace element compositions of corresponding groundwaters: ophiolite detritus in OMM sandstones in western Switzerland (Cr), barite fracture mineralisations in subalpine and folded Molasse units (Ba), granitic detritus containing sulphides (Mo), U-minerals (U) and abundant mica (Li) in the "Glimmersand" (OSM, Ca-Mg-HCO3-SO4 waters), and evaporite minerals (Li, Sr), sulphides (Mo), and U-minerals (U) in the "Gypsum-bearing Molasse" (USM, highly mineralised Ca-Mg-SO4-HCO3 waters, TDS 984 to 1346 mg/L) . In these molasse groundwaters the Swiss quality target values for drinking water of Cr and Pb are exceeded in 36% and 6% of the springs, respectively. The U concentrations of 14% of the molasse groundwaters ("Gypsum-bearing Molasse" and "Glimmersand"), exceed the WHO guideline value. The groundwaters from the "Gypsum-bearing Molasse" display similar quality problems as the evaporite groundwaters. Groundwaters derived from the shallow flysch aquifers in the Niesen and Gurnigel nappes are poorly evolved Ca-(Mg)-HCO3 waters. Their low to intermediate total mineralisation (TDS 160 to 459 mg/L) is acquired primarily by dissolution of calcite and to a lesser degree dolomite. The low trace element content is dominated by Ba originating from barite fracture mineralisations. The poor chemical evolution of recent flysch groundwaters results from (1) their short residence time in the fractured flysch rocks, and (2) the absence of readily dissolving minerals except carbonates and barite. In 32% of the flysch springs Pb derived from atmospheric sources exceeds the Swiss quality target value. 2.) Case study on the chemical weathering of molasse sandstone: Sources and chemical behaviour of Cr For the characterisation of the potentially toxic tracer element Cr a comprehensive field study was carried out on a selected catchment (Lutry spring catchment near Lausanne) situated in a molasse sandstone (OMM, Burdigalian). The investigation of the processes controlling the dissolved Cr content in these groundwaters was based on the groundwater chemical data, as well as on mineralogical, geochemical, and hydrological data. Relic Cr-bearing spinel and pyroxene in the sandstone were identified to be the primary sources of Cr. An electron microscope study showed that in the Burdigalian sandstone and overlying soil these minerals are strongly weathered. The slow weathering of these minerals is the major Cr releasing process. Under the oxidising conditions reigning in the investigated groundwaters, Cr prevails in solution in its highly soluble and toxic hexavalent state (CrO42-). In this case, retention by secondary Cr-hydroxide phases does not occur, as can be shown by geochemical model calculations. Laboratory leaching experiments were carried out with Burdigalian molasse sandstone from the field site, in order to support the field study findings and to quantify the processes responsible for the Cr mineralisation observed in the Lutry groundwater. Two experiments with mountain-wet oxidised and reduced sandstone were carried out over a time span of 2 months each, to obtain information about the influence of the oxidation state of the substratum on the mobilisation of Cr. The experiments clearly showed that the Cr-releasing processes are fast enough to explain the Cr contents found in the groundwater, and that the release of Cr into the groundwater depends on the weathering state of the sandstone. In the oxidised, Fe-hydroxide-coated sandstone, Cr is faster released into solution than in the less altered reduced sandstone. This indicates that the Cr contained in the reduced sandstone is in a more stable state, i.e. mainly incorporated in detrital minerals, while in the oxidised sandstone, the Cr is partly in an unstable state, i.e. adsorbed on the surface of secondary Fe-hydroxides, from where it is more easily leached.

EPFL2001