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Lu, C.; Xin, P.; Kong, J.; Li, L.; Luo, J. |
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Title |
Analytical solutions of seawater intrusion in sloping confined and unconfined coastal aquifers |
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Journal Article |
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2016 |
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Water Resources Research |
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52 |
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9 |
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6989-7004 |
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Keywords |
seawater intrusion, sloping coastal aquifer, analytical solution |
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Abstract Sloping coastal aquifers in reality are ubiquitous and well documented. Steady state sharp-interface analytical solutions for describing seawater intrusion in sloping confined and unconfined coastal aquifers are developed based on the Dupuit-Forchheimer approximation. Specifically, analytical solutions based on the constant-flux inland boundary condition are derived by solving the discharge equation for the interface zone with the continuity conditions of the head and flux applied at the interface between the freshwater zone and the interface zone. Analytical solutions for the constant-head inland boundary are then obtained by developing the relationship between the inland freshwater flux and hydraulic head and combining this relationship with the solutions of the constant-flux inland boundary. It is found that for the constant-flux inland boundary, the shape of the saltwater interface is independent of the geometry of the bottom confining layer for both aquifer types, despite that the geometry of the bottom confining layer determines the location of the interface tip. This is attributed to that the hydraulic head at the interface is identical to that of the coastal boundary, so the shape of the bed below the interface is irrelevant to the interface position. Moreover, developed analytical solutions with an empirical factor on the density factor are in good agreement with the results of variable-density flow numerical modeling. Analytical solutions developed in this study provide a powerful tool for assessment of seawater intrusion in sloping coastal aquifers as well as in coastal aquifers with a known freshwater flux but an arbitrary geometry of the bottom confining layer. |
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THL @ christoph.kuells @ Lu.etal.2016 |
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15 |
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Cary, L.; Petelet-Giraud, E.; Bertrand, G.; Kloppmann, W.; Aquilina, L.; Martins, V.; Hirata, R.; Montenegro, S.M.G.L.; Pauwels, H.; Chatton, E.; Franzen, Melissa; Aurouet, A.; Lasseur, E.; Picot-Colbeaux, G.; Guerrot, C.; Fléhoc, C.; Labasque, T.; Santos, Jeane Glaucia; Paiva, Anderson L.R.; Braibant, G.; Pierre, D. |
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Origins and processes of groundwater salinization in the urban coastal aquifers of Recife (Pernambuco, Brazil): a multi-isotope approach |
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Journal Article |
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2015 |
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Science of the Total Environment |
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530-531 |
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411-429 |
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Salinization origins; Salinization processes; Groundwater; Coastal aquifer; Strontium isotopes; Boron isotopes; Recife; Brazil |
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Elsevier |
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THL @ christoph.kuells @ cary:hal-01161949 |
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85 |
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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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Hydrogeochemical and isotopic evidence of groundwater salinization in a coastal aquifer: a case study in Jeju volcanic island, Korea |
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2003 |
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Journal of Hydrology |
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270 |
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3 |
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282-294 |
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Jeju volcanic island, Coastal aquifer, Groundwater salinization, Hydrogeochemistry, Environmental isotopes, Mixing process |
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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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Han, D.M.; Song, X.F.; Currell, M.J.; Yang, J.L.; Xiao, G.Q. |
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Chemical and isotopic constraints on evolution of groundwater salinization in the coastal plain aquifer of Laizhou Bay, China |
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2014 |
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Journal of Hydrology |
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508 |
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12-27 |
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Laizhou Bay, Coastal aquifers, Groundwater hydrochemistry, Stable isotopes, Saltwater intrusion |
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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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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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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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2016 |
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Science of The Total Environment |
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566-567 |
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398-415 |
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Groundwater salinization, Coastal aquifer, Roussillon Basin, Isotopes, Westbay System, Barcarès and Canet sites |
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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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