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Author |
Jesús Carrera, Juan J. Hidalgo, Luit J. Slooten, Enric Vázquez-Suñé |
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Title |
Computational and conceptual issues in the calibration of seawater intrusion models |
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Journal Article |
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Year |
2010 |
Publication |
Hydrogeology Journal |
Abbreviated Journal |
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Volume |
18 |
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Pages |
131-145 |
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Keywords  |
Coastal aquifers; Inverse modelling; Numerical modeling |
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Abstract |
The inverse problem of seawater intrusion(SWI) is reviewed. It represents a challenge because of both conceptual and computational difficulties and because coastal aquifer models display many singularities:(1) head measurements need to be complemented with density information; (2) salinity concentration data are
very sensitive to flow within the borehole. Data problems can be reduced by incorporating the measurement process within model calibration; (3) SWI models are extremely sensitive to aquifer bottom topography; (4) the initial conditions may be far from steady state and depend on the location and type of sea-aquifer connection. Problems with aquifer geometry and initial conditions can be addressed by parameterization, which allows for modification during inversion. The four sets of difficulties can be partly overcome by using tidal response and electrical conductivity data, which are highly informative and
provide extensive coverage. Still, SWI inversion is extremely demanding from a computation point of view. Computational improvements are discussed. |
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J. Carrera : J. J. Hidalgo ()) : L. J. Slooten : E. Vázquez-Suñé, Spain e-mail: juan.hidalgo@upc.edu |
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Corporate Author |
Institute of Environmental Ass Institute of Environmental Assessment and Water Research (IDAEA), Spanish National Research Council (CSIC), Jordi Girona 18, 08034 Barcelona, e-mail: juan.hidalgo@upc.edu |
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IAH |
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Springer |
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English |
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1431- 2174 (online: 1435-0157) |
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'Hydrogeology'; 'groundwater modelling' |
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yes |
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Call Number |
MGRE @ redha.menani @ |
Serial |
51 |
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Author |
Petelet-Giraud, E.; Négrel, P.; Aunay, B.; Ladouche, B.; Bailly-Comte, V.; Guerrot, C.; Flehoc, C.; Pezard, P.; Lofi, J.; Dörfliger, N. |
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Title |
Coastal groundwater salinization: Focus on the vertical variability in a multi-layered aquifer through a multi-isotope fingerprinting (Roussillon Basin, France) |
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Journal Article |
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Year |
2016 |
Publication |
Science of The Total Environment |
Abbreviated Journal |
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Volume |
566-567 |
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Pages |
398-415 |
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Keywords |
Groundwater salinization, Coastal aquifer, Roussillon Basin, Isotopes, Westbay System, Barcarès and Canet sites |
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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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Author |
Sarker, M.M.R.; Van Camp, M.; Islam, M.; Ahmed, N.; Walraevens, K. |
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Title |
Hydrochemistry in coastal aquifer of southwest Bangladesh : origin of salinity |
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Journal Article |
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Year |
2018 |
Publication |
Environmental Earth Sciences |
Abbreviated Journal |
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Volume |
77 |
Issue |
2 |
Pages |
20 |
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Keywords |
Hydrochemistry,Stable isotope,Seawater intrusion,Coastal aquifer,Bangladesh,DAR-ES-SALAAM,SEAWATER INTRUSION,DELTA PLAIN,GROUNDWATER,DRINKING,TANZANIA,DROUGHT,COMPLEX |
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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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Kim, Y.; Lee, K.-S.; Koh, D.-C.; Lee, D.-H.; Lee, S.-G.; Park, W.-B.; Koh, G.-W.; Woo, N.-C. |
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Title |
Hydrogeochemical and isotopic evidence of groundwater salinization in a coastal aquifer: a case study in Jeju volcanic island, Korea |
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Journal Article |
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Year |
2003 |
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Journal of Hydrology |
Abbreviated Journal |
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270 |
Issue |
3 |
Pages |
282-294 |
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Keywords |
Jeju volcanic island, Coastal aquifer, Groundwater salinization, Hydrogeochemistry, Environmental isotopes, Mixing process |
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Abstract |
In order to identify the origin of saline groundwater in the eastern part of Jeju volcanic island, Korea, a hydrogeochemical and isotopic study has been carried out for 18 observation wells located in east and southeast coastal regions. The total dissolved solid contents of groundwaters are highly variable (77–21,782mg/l). Oxygen, hydrogen, sulfur, and strontium isotopic data clearly show that the saline water results from mixing of groundwater with seawater. Strontium isotopic compositions and Br/Cl and I/Cl ratios strongly suggest that the source of salinity is modern seawater intrusion. Hydrogeochemical characteristics based on bivariate diagrams of major and minor ions show that changes in the chemical composition of groundwater are mainly controlled by the salinization process followed by cation-exchange reactions. The highly permeable aquifers at the east coastal region are characterized by low hydraulic gradient and discharge rate and high hydraulic conductivity as compared with other regions. These properties enhance the salinization of groundwater observed in the study area. Based on the Cl, Br, and δ18O data, seawater was determined to have intruded inland some 2.5km from the coastline. Considering the poor correlation of sampling depth and Cl concentrations observed, the position of seawater-freshwater interface is not uniformly distributed in the study area, due to heterogeneities of the basaltic aquifers. |
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0022-1694 |
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THL @ christoph.kuells @ Kim2003282 |
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172 |
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Author |
Han, D.M.; Song, X.F.; Currell, M.J.; Yang, J.L.; Xiao, G.Q. |
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Title |
Chemical and isotopic constraints on evolution of groundwater salinization in the coastal plain aquifer of Laizhou Bay, China |
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Journal Article |
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Year |
2014 |
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Journal of Hydrology |
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508 |
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12-27 |
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Keywords |
Laizhou Bay, Coastal aquifers, Groundwater hydrochemistry, Stable isotopes, Saltwater intrusion |
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Abstract |
Summary A hydrochemical-isotopic investigation of the Laizhou Bay Quaternary aquifer in north China provides new insights into the hydrodynamic and geochemical relationships between freshwater, seawater and brine at different depths in coastal sediments. Saltwater intrusion mainly occurs due to two cones of depression caused by concentrated exploitation of fresh groundwater in the south, and brine water for salt production in the north. Groundwater is characterized by hydrochemical zonation of water types (ranging from Ca–HCO3 to Na–Cl) from south to north, controlled by migration and mixing of saline water bodies with the regional groundwater. The strong adherence of the majority of ion/Cl ratios to mixing lines between freshwater and saline water end-members (brine or seawater) indicates the importance of mixing under natural and/or anthropogenic influences. Examination of the groundwater stable isotope δ18O and δ2H values (between −9.5‰ and −3.0‰ and −75‰ and −40‰, respectively) and chloride contents (∼2 to 1000meq/L) of the groundwater indicate that the saline end-member is brine rather than seawater, and most groundwater samples plot on mixing trajectories between fresh groundwater (δ18O of between −6.0‰ and −9.0‰; Cl<5meq/L) and sampled brines (δ18O of approximately −3.0‰ and Cl>1000meq/L). Locally elevated Na/Cl ratios likely result from ion exchange in areas of long-term freshening. The brines, with radiocarbon activities of ∼30 to 60 pMC likely formed during the Holocene as a result of the sequence of transgression-regression and evaporation; while deep, fresh groundwater with depleted stable isotopic values (δ18O=−9.7‰ and δ2H=−71‰) and low radiocarbon activity (<20 pMC) was probably recharged during a cooler period in the late Pleistocene, as is common throughout northern China. An increase in the salinity and tritium concentration in some shallow groundwater sampled in the 1990s and re-sampled here indicates that intensive brine extraction has locally resulted in rapid mixing of young, fresh groundwater and saline brine. The δ18O and δ2H values of brines (∼−3.0‰ and −35‰) are much lower than that of modern seawater, which could be explained by 1) mixing of original (δ18O enriched) brine that was more saline than presently observed, with fresh groundwater recharged by precipitation and/or 2) dilution of the palaeo-seawater with continental runoff prior to and/or during brine formation. The first mechanism is supported by relatively high Br/Cl molar ratios (1.7×10−3–2.5×10−3) in brine water compared with ∼1.5×10−3 in seawater, which could indicate that the brines originally reached halite saturation and were subsequently diluted with fresher groundwater over the long-term. Decreasing 14C activities with increasing sampling depth and increasing proximity to the coastline indicate that the south coastal aquifer in Laizhou Bay is dominated by regional lateral flow, on millennial timescales. |
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0022-1694 |
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THL @ christoph.kuells @ Han201412 |
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174 |
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