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| Author |
Sebben, M.L.; Werner, A.D.; Graf, T. |
| Title |
Seawater intrusion in fractured coastal aquifers: A preliminary numerical investigation using a fractured Henry problem |
Type |
Journal Article |
| Year |
2015 |
Publication |
Advances in Water Resources |
Abbreviated Journal |
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| Volume |
85 |
Issue |
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Pages |
93-108 |
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| Abstract |
Despite that fractured coastal aquifers are widespread, the influence of fracture characteristics on seawater intrusion (SWI) has not been explored in previous studies. This research uses numerical modelling in a first step towards understanding the influence of fracture orientation, location and density on the extent of seawater and accompanying patterns of groundwater discharge in an idealised coastal aquifer. Specifically, aquifers containing single fractures or networks of regularly spaced fractures are studied using modified forms of the Henry SWI benchmark problem. The applicability of equivalent porous media (EPM) models for representing simple fracture networks in steady-state simulations of SWI is tested. The results indicate that the influence of fractures on SWI is likely to be mixed, ranging from enhancement to reduction in seawater extent and the width of the mixing zone. For the conceptual models considered here, vertical fractures in contact with the seawater wedge increase the width of the mixing zone, whereas vertical fractures inland of the wedge have minimal impact on the seawater distribution. Horizontal fractures in the lower part of the aquifer force the wedge seaward, whereas horizontal fractures located within the zone of freshwater discharge enhance the wedge. Inclined fractures roughly parallel to the seawater-freshwater interface increase the landward extent of seawater and fractures perpendicular to the interface inhibit the wedge. The results show that EPM models are likely inadequate for inferring salinity distributions in most of the fractured cases, although the EPM approach may be suitable for orthogonal fracture networks if fracture density is high and appropriate dispersivity values can be determined. |
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0309-1708 |
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THL @ christoph.kuells @ Sebben2015 |
Serial |
37 |
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| Author |
Sarker, M.M.R.; Van Camp, M.; Islam, M.; Ahmed, N.; Walraevens, K. |
| Title |
Hydrochemistry in coastal aquifer of southwest Bangladesh : origin of salinity |
Type |
Journal Article |
| Year |
2018 |
Publication |
Environmental Earth Sciences |
Abbreviated Journal |
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| Volume |
77 |
Issue |
2 |
Pages |
20 |
| Keywords |
Hydrochemistry,Stable isotope,Seawater intrusion,Coastal aquifer,Bangladesh,DAR-ES-SALAAM,SEAWATER INTRUSION,DELTA PLAIN,GROUNDWATER,DRINKING,TANZANIA,DROUGHT,COMPLEX |
| Abstract |
In the coastal region of Bangladesh, groundwater is mainly used for domestic and agricultural purposes, but salinization of many groundwater resources limits its suitability for human consumption and practical application. This paper reports the results of a study that has mapped the salinity distribution in different aquifer layers up to a depth of 300 m in a region bordering the Bay of Bengal based on the main hydrochemistry and has investigated the origin of the salinity using Cl/Br ratios of the samples. The subsurface consists of a sequence of deltaic sediments with an alternation of more sandy and clayey sections in which several aquifer layers can be recognized. The main hydrochemistry shows different main water types in the different aquifers, indicating varying stages of freshening or salinization processes. The most freshwater, soft NaHCO3-type water with Cl concentrations mostly below 100 mg/l, is found in the deepest aquifer at 200-300 m below ground level (b.g.l.), in which the fresh/saltwater interface is pushed far to the south. Salinity is a main problem in the shallow aquifer systems, where Cl concentrations rise to nearly 8000 mg/l and the groundwater is mostly brackish NaCl water. Investigation of the Cl/Br ratios has shown that the source of the salinity in the deep aquifer is mixing with old connate seawater and that the saline waters in the more shallow aquifers do not originate from old connate water or direct seawater intrusion, but are derived from the dissolution of evaporite salts. These must have been formed in a tidal flat under influence of a strong seasonal precipitation pattern. Long dry seasons with high evaporation rates have evaporated seawater from inundated gullies and depressions, leading to salt precipitation, while subsequent heavy monsoon rains have dissolved the formed salts, and the solution has infiltrated in the subsoil, recharging groundwater. |
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1866-6280 |
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THL @ christoph.kuells @ Sarker2018 |
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194 |
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Russak, A.; Sivan, O.; Yechieli, Y. |
| Title |
Trace elements (Li, B, Mn and Ba) as sensitive indicators for salinization and freshening events in coastal aquifers |
Type |
Journal Article |
| Year |
2016 |
Publication |
Chemical Geology |
Abbreviated Journal |
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441 |
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Pages |
35-46 |
| Keywords |
Seawater intrusion, Fresh-saline water interface, Trace metal, Manganese, Lithium, Boron |
| Abstract |
The current global intrusion of seawater into coastal aquifers causes salinization of groundwater and thus significant degradation of its quality. This study quantified the effect of seawater intrusion and freshening events in coastal aquifers on trace elements (Li, B, Mn and Ba) across the fresh-saline water interface (FSI) and their possible use as indicators for these events. This was done by combining field data and column experiments simulating these events. The experiments enabled quantification of the processes affecting the trace element composition and examination of whether salinization and freshening events are geochemically reversible, which has been seldom investigated. The dominant process affecting trace element composition during salinization and freshening is ion exchange. The results of the experiments show that the concentrations of major cations and Li+ were reversible during salinization and freshening, whereas B, Mn2+ and Ba2+ were not. During salinization, Li+ and B were depleted due to sorption by 10 and 100μmol·L−1, respectively, to about half of their expected conservative concentrations. The relative depletion of Li+ increased with distance from the shore, representing the propagation of salinization. Ba2+ and Mn2+ were desorbed from the sediment during salinization and enriched by tenfold in the aqueous phase compared to their concentration in seawater ( 0.1 μeq·L−1). During freshening both were depleted by almost tenfold compared to their concentration in fresh groundwater ( 0.7 μeq·L−1). The depletion of Mn2+ is a sensitive marker for freshening because Mn2+ has a strong affinity to the solid phase. Moreover, this study shows that both Mn2+ and Ba2+ can be used as sensitive hydrogeochemical tools to distinguish between salinization and freshening events in the FSI zone in coastal aquifers. |
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en |
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0009-2541 |
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THL @ christoph.kuells @ Russak201635 |
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197 |
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Post, V.E.A.; Houben, G.J.; van Engelen, J. |
| Title |
What is the Ghijben-Herzberg principle and who formulated it? |
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Journal Article |
| Year |
2018 |
Publication |
Hydrogeology Journal |
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26 |
Issue |
6 |
Pages |
1801-1807 |
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It has been suggested in a number of historical notes that it was neither Willem Badon Ghijben nor Alexander Herzberg who formulated the famous principle now carrying their name, which relates the water-table elevation to the depth of the freshwater saltwater interface in coastal aquifers. In this paper, a systematic review of the literature pre-dating the publication of their work is presented. The aim is to establish to what extent these previous works captured the essence of the Ghijben-Herzberg principle, that is, the combination of a correct conceptual model of the hydrogeological conditions with a quantitative relationship. It was found that references to coastal fresh groundwater reserves can be traced back to Roman times, while the earliest detailed descriptions of a freshwater lens that could be found dates from the eighteenth century. The correct understanding of the hydrostatic equilibrium between fresh and salt groundwater is evident in works from the early nineteenth century. However, it was Badon Ghijben and Herzberg who combined this with the correct understanding of the groundwater conditions of a freshwater lens. It was further found that Herzberg had already recorded his findings in 1888 in a hand-written report, confirming speculation that such a report might exist. |
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1435-0157 |
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THL @ christoph.kuells @ Post2018 |
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89 |
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Petelet-Giraud, E.; Négrel, P.; Aunay, B.; Ladouche, B.; Bailly-Comte, V.; Guerrot, C.; Flehoc, C.; Pezard, P.; Lofi, J.; Dörfliger, N. |
| Title |
Coastal groundwater salinization: Focus on the vertical variability in a multi-layered aquifer through a multi-isotope fingerprinting (Roussillon Basin, France) |
Type |
Journal Article |
| Year |
2016 |
Publication |
Science of The Total Environment |
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566-567 |
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Pages |
398-415 |
| Keywords |
Groundwater salinization, Coastal aquifer, Roussillon Basin, Isotopes, Westbay System, Barcarès and Canet sites |
| Abstract |
The Roussillon sedimentary Basin (South France) is a complex multi-layered aquifer, close to the Mediterranean Sea facing seasonally increases of water abstraction and salinization issues. We report geochemical and isotopic vertical variability in this aquifer using groundwater sampled with a Westbay System® at two coastal monitoring sites: Barcarès and Canet. The Westbay sampling allows pointing out and explaining the variation of water quality along vertical profiles, both in productive layers and in the less permeable ones where most of the chemical processes are susceptible to take place. The aquifer layers are not equally impacted by salinization, with electrical conductivity ranging from 460 to 43,000μS·cm−1. The δ2H–δ18O signatures show mixing between seawater and freshwater components with long water residence time as evidenced by the lack of contribution from modern water using 3H, 14C and CFCs/SF6. S(SO4) isotopes also evidence seawater contribution but some signatures can be related to oxidation of pyrite and/or organically bounded S. In the upper layers 87Sr/86Sr ratios are close to that of seawater and then increase with depth, reflecting water–rock interaction with argillaceous formations while punctual low values reflect interaction with carbonate. Boron isotopes highlight secondary processes such as adsorption/desorption onto clays in addition to mixings. At the Barcarès site (120m deep), the high salinity in some layers appear to be related neither to present day seawater intrusion, nor to Salses-Leucate lagoonwater intrusion. Groundwater chemical composition thus highlights binary mixing between fresh groundwater and inherited salty water together with cation exchange processes, water–rock interactions and, locally, sedimentary organic matter mineralisation probably enhanced by pyrite oxidation. Finally, combining the results of this study and those of Caballero and Ladouche (2015), we discuss the possible future evolution of this aquifer system under global change, as well as the potential management strategies needed to preserve quantitatively and qualitatively this water resource. |
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0048-9697 |
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THL @ christoph.kuells @ Peteletgiraud2016398 |
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181 |
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