Groundwater flow

Summary

In hydrogeology, groundwater flow is defined as the "part of streamflow that has infiltrated the ground, entered the phreatic zone, and has been (or is at a particular time) discharged into a stream channel or springs; and seepage water." It is governed by the groundwater flow equation. Groundwater is water that is found underground in cracks and spaces in the soil, sand and rocks. Where water has filled these spaces is the phreatic (also called) saturated zone. Groundwater is stored in and moves slowly (compared to surface runoff in temperate conditions and watercourses) through layers or zones of soil, sand and rocks: aquifers. The rate of groundwater flow depends on the permeability (the size of the spaces in the soil or rocks and how well the spaces are connected) and the hydraulic head (water pressure). In polar regions groundwater flow may be obstructed by permafrost. See also *Subsurface flow *Groundwater energy balance *Baseflow *Ecohydrology *Groundwater *Hydro

Official source

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Related publications (15)

High spatial and temporal resolution water temperature measurements, using DTS, allow to model and to control stream temperature evolution in the Tambarga’s basin (Burkina Faso). A wireless sensor network recorded solar radiation, air temperature, air humidity, wind speed (among others) on different sites on Tambarga’s basin (B.F.) in 2009. These data are compiled and used as inputs to force the model and to assess simulated river temperatures in the basin. Local parameters as shade coefficient, stream bed heat losses as well as land coverage coefficient are estimated from on field knowledge. Purpose but also need for this study, stream discharge estimation in the Tambarga’s river is paramount. Discharges are formed by subsurface flow, groundwater flow and runoff during rain events. Assuming that all three water discharge components have a different thermal signature leads to imagine that they can be identified with the DTS optical fiber, once they reach the main stream. The inflow emplacements are referred to as springs in this study. Finally, although this study leads to significant results, the last sections propose the installation of some more measuring instruments for controlling and improving the model accuracy.

2010

Contribution à l'étude du comportement thermo-hydraulique du stockage de chaleur en aquifère

Stéphane Dupasquier

In this work, a parametric study is done with computational methods for groundwater flow and heat transport in order to describe the dominant physical phenomena in an Aquifer Thermal Energy Storage (ATES). Optimum operating conditions and geological parameters are deduced from it. The intended use of the ATES is the domestic water or space heating. The stock is seasonal and functions without heat pump. Parametric study is organized as a series of reference simulations relating to the thickness of the aquifer and the injection flow rate. The other parameters and operating conditions of are kept constant. Other simulations are done and compared to the reference simulations in order to describe the influence of injection temperature, hydraulic conductivity, anisotropicity, injection frequencies, phases of rest, outflow rate and doublet wells. The cells of natural convection are strongly affecting the performances of an ATES. The thermal losses by conduction trough bedrock and caprock is an unfavourable factor as well, but to a lesser extent however. The increase of inflow rate always improves the efficiency, whereas an optimum aquifer thickness exists for each inflow rate. This optimum is characterised by weak natural convection phenomena. A greater thickness means strong density-viscosity effects, while a thinner aquifer forms a horizontally stretched stock, with increased conductive losses through the bedrock and cap rock. A maximum thermal recovery rate exists for a given flow rate. This maximum increases with inflow rate. The injection temperature behaves on the stock in the same way as the aquifer thickness for a given inflow: there is an optimal temperature. However it is in general preferable to increase the injection temperature instead of the inflow rate. In terms of optimization of the thermal power at disposal, the most favorable scenario is an increasing flow during the discharge. The precise scenario is different for each problem. The performances of a ATES are the complex result of the many parameters which enter in plays. One will recommend an inflow rate of at least 100m33/d during 6 months, and even rather 500 - 1000m3/d with an injection temperature of 80°C at least. An injection temperature of 60°C will have to be associated with an inflow of 1000m3/d at least. The geological targets proposed in Switzerland are the quaternary alluvial deposits filling the former glaciated valleys, fluvioglacial deposits and alluvial fans.

EPFL2001

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

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EPFL2001