Geochemical and isotopic evidence for palaeo-seawater intrusion into the south coast aquifer of Laizhou Bay, China

This research aims to improve the current knowledge of groundwater salinisation processes in coastal aquifers using combined hydrochemical and isotopic parameters and inverse hydrochemical modelling. Field investigations were conducted in Laizhou Bay, which is the area most seriously affected by seawater intrusion in north China. During three sampling campaigns along a vertical transect in the Changyi-Liutuan area, 95 ground- and surface-water samples were collected for major ion and isotope analysis (²H/¹⁸O, ³H, ¹⁴C, ³⁴S). The groundwater changes along the general flowpath towards the coast from fresh (<1 g/L), brackish (1-10 g/L), saline (10-100 g/L) to brine water (>100 g/L). Molar Cl/Br ratios are close to those of seawater in almost all groundwater samples, indicating that brines and deep seawater evolved from different events of palaeo-seawater intrusion. Depleted isotopic signatures of brines and deep saline water point to a former, initially depleted seawater reservoir due to runoff dilution. Tritium and ¹⁴C activities in deep saline water below confining units indicate isolation from modern precipitation and significant residence times. Brine water shows a wide range of ³H and ¹⁴C ages due to the complex conditions of mixing without isolation from modern groundwater. Sulphur-34 isotope ratios support seawater intrusion as a possible salt origin, although this parameter does not exclude gypsum dissolution. The combined use of Cl and ¹⁸O yields four different end-members of groundwater, and three different mixing scenarios were identified explaining the hydrochemical composition of groundwater samples with intermediate salinity in the different areas. To improve understanding of the various water types and their related processes in a spatial context, a conceptual model was developed integrating the results derived from the presented data in a vertical cross-section. Results of three inverse modelling simulations using PHREEQC-2 show that all hypothetical mixing scenarios derived from conservative components are thermodynamically feasible. In all scenarios, mixing, ion exchange, dissolution of dolomite and precipitation of gypsum and calcite account for the hydrochemical changes.     

Hydrogeochemical Analysis of Processes Through Modeling of Seawater Intrusion Impacts in Biscayne Aquifer Water Quality,USA

Hydrogeochemical processes that accompany seawater intrusion in coastal aquifers can alter the resulting water quality and are important ingredients in coastal aquifer management. The presence of dissolution–precipitation reactions and ion exchange in the mixing zone of the Biscayne aquifer (FL, USA) are suggested based on changes in major ion concentrations and mineral saturation indices (SI). Major ion concentrations from 11 groundwater samples are compared with theoretical mixing between freshwater and seawater. PHREEQC code was used to calculate saturation indices of the samples with respect to common phases in the Biscayne aquifer. High Ca²⁺ and HCO₃ ^? content of the samples is typical of waters in contact with carbonate aquifers. Water quality of the samples is mainly attributed to mixing and precipitation–dissolution reactions with calcite and dolomite. The samples were saturated with calcite (SI ~ 0) and undersaturated for dolomite (SI < 0), while a few samples showed dolomite saturation. Because gypsum and halite SI could be predicted by theoretical mixing, reactions with those minerals, if present, are thought to be insignificant. In the active intrusion areas, cation exchange also appears to modify water quality leading to excess Ca²⁺, but depleted Na⁺, Mg²⁺ and K⁺ concentrations. On the other hand, samples from previous intrusion areas plotted very close to the theoretical mixing line and approached equilibrium with the seawater.     

Factors controlling mechanisms of groundwater salinization and hydrogeochemical processes in the Quaternary aquifer of the Eastern Nile Delta, Egypt

In this study, combining interpretations of conservative dissolved ions and environmental isotopes in water were used to investigate the main factors and mechanisms controlling groundwater salinization and hydrogeochemical processes in the Eastern Nile Delta, Egypt. Hydrogeochemical and isotopic study has been carried out for 61 water samples from the study area. Total dissolved solid (TDS) contents of groundwater are highly variable rising along flowpath from the south (410 mg/L) to the north (14,784 mg/L), implying significant deterioration and salinization of groundwater. Based on TDS and ionic ratios, groundwater samples were classified into three groups. In low-saline groups, water chemistry is greatly influenced by cation exchange, mineral dissolution/precipitation, anthropogenic pollutants and mixing with surface water. Whilst, in high-saline groups, water chemistry is affected by salt-water intrusion, reverse cation exchange and evaporation. The chemical constituents originating from saline water sources, reverse ion exchange and mineral dissolution are successfully differentiated using ionic delta and saturation index approaches. The δ¹⁸O–δ²H relationship plots on a typical evaporation line, suggesting potential evaporation of the recharging water prior to infiltration. Isotope evidence concludes that the groundwater have been considerably formed by mixing between depleted meteoric water recharged under different climatic conditions and recently infiltrating enriched surface water and excess of irrigation water. The δ¹⁸O data in conjunction with chloride concentrations provide firm evidence for impact of dissolution of marine-origin evaporite deposits, during past geologic periods, on groundwater salinity in the northern region. Moreover, the relation between ¹⁴C activities and Cl^? concentration confirms this hypothesis.     

Origin of groundwater salinity in the Fasa Plain,southern Iran,hydrogeochemical and isotopic approaches

The study area, the Fasa Plain, is situated in the semiarid region of Fars Province in the south of Iran. The Salloo diapir is a salt dome that crops out in the northwest of the study area. Isotopic and hydrochemical analyses were used to examine the water and how the origin of salinity and the diapir affect the quality of the groundwater quality in the study area. Groundwater was sampled from 31 representative pumping wells in alluvial aquifer and five springs in order to measure their stable isotope compositions, bromide ion concentration, and physical and chemical parameters. The alluvial aquifer was organized into two main groups based on the chemistry, with Group 1 consisting of low-salinity well samples (544–1744 µS/cm) with water type Ca–Mg–HCO₃–SO₄ which were taken in the center and north of the area, and Group 2 consisting of high-salinity samples (2550–4620 µS/cm) with water type Ca–Mg–Cl–SO₄ which were taken from the wells in the south and southwest of the area. A saline spring near the salt dome with an EC of 10,280 µS/cm has water type Na–Cl, while the compositions of the water in the other karstic springs is comparable to the fresh groundwater samples. All groundwater samples are undersaturated with respect to gypsum, anhydrite, and halite and are supersaturated with respect to calcite and dolomite. Stable isotopes (δ¹⁸O and δ²H) differentiated four water types: saline springs, freshwater spring, fresh groundwater, and saline groundwater. The results indicate that meteoric water is the main origin of these water resources. Halite dissolution from the salt dome was identified as the origin of salinity. The Na/Cl and Cl/Br ratios confirmed the results. Groundwater compositions in the southwestern part of the area are affected by the intrusion of saltwater from the salt dome. The average saltwater fraction in the some water wells is about 0.2%. In the south and southwestern part of the area, the saltwater fraction is positive in mixed freshwater/saltwater (Group 2). Different processes interact together to change the hydrochemical properties of Fasa’s alluvial aquifer. The main processes that occur in the aquifer are mixing, gypsum dissolution, and calcite precipitation.     

Geochemical evolution and timescale of seawater intrusion into the coastal aquifer of Israel

This study is an attempt to quantify the geochemical processes and the timescale of seawater intrusion into a coastal aquifer from changes in the major ionic composition of the water and the natural distribution of the cosmogenic isotopes ¹⁴C and ³H. For that purpose, we sampled saline and brackish groundwaters from the Israeli coastal aquifer. A multilayer sampler (MLS) was used to obtain very high resolution (10 cm) profiles across the fresh-saline water interface (FSI).The chemical and stable isotope data revealed three distinct water types (end members) that are located in different zones on the route to the coastal aquifer: (1) slightly modified Mediterranean seawater (SWS); (2) slightly diluted (with up to 20% fresh groundwater) saline groundwater (SDS); and (3) fresh groundwater (FGW).The SWS samples generally show an excess of total alkalinity and total dissolved inorganic carbon (DIC), and a depletion of ¹³C_DIC and ¹⁴C_DIC with respect to normal seawater indicating that anaerobic oxidation of organic matter is the first diagenetic reaction that affects seawater during its penetration into the bottom sediments. SDS waters appear when SWS is slightly diluted, gain Ca²⁺ and Sr²⁺, and is depleted in K⁺, suggesting that the main processes that transform SWS into SDS are slight dilution with fresh groundwater and cation exchange. At the fresh-saline water interface, SDS generally shows conservative mixing with FGW.Inspection of chemical data from coastal aquifers around the world indicates that intensive ion exchange in slightly diluted saline groundwater is a globally important phenomenon of seawater intrusion. Most of our saline groundwater samples contain substantial amounts of ³H suggesting that penetration of Mediterranean seawater and its inland travel to a distance of 50-100 m onshore occurred 15-30 yr ago. This is supported by the ¹⁴C_DIC mass balance that explains the relatively low ¹⁴C_DIC activities in the SDS as influenced by diagenesis and not by simple radioactive decay.     

Hydrogeochemistry and geochemical simulations to assess water–rock interactions in complex carbonate aquifers: The case of Aguadulce (SE Spain)

The hydrogeological unit of Aguadulce (Campo de Dalías aquifers, SE Spain) has a complex geometry. This fact, together with a continuous rise in water demand due to intensive agriculture and tourism create problems for groundwater quantity and quality. In this paper classic geochemical tools managed by means of GIS software and geochemical simulations are combined to delineate, identify and locate the possible physicochemical processes acting in the Aguadulce groundwater. Two main aquifers can be distinguished: the carbonate or lower aquifer of Triassic age, and the calcodetritic or upper aquifer of Plio-Quaternary age. Groundwaters from the latter are more saline and, assuming all chlorinity originates from seawater intrusion, the seawater contribution to their composition would be up to 7%. Nevertheless the carbonate aquifer appears not to be homogeneous: it is compartmentalised into 4 zones where different processes explain the different groundwaters compositions. Zone 4 samples (E margin of the carbonate aquifer) resemble those of the Plio-Quaternary aquifer, where calcite precipitation, dolomite and gypsum dissolution and some cation exchange (water–rock interaction) together with seawater–freshwater mixing occur. In contrast, water–rock interaction predominates in zones 1 and 3 of the carbonate aquifer. Moreover, zone 2 samples, located between zones 1 and 3, are explained by water–rock interaction in addition to mixing with Plio-Quaternary aquifer waters. The combination of geochemical simulations with GIS and hydrogeochemical analyses has proven to be effective in identifying and locating the different physicochemical processes in the aquifer areas, thus improving understanding of hydrogeochemistry in complex aquifers.     

Geochemical process regulating groundwater quality in a coastal region with complex contamination sources: Barka,Sultanate of Oman

An investigation was carried out to evaluate the geochemical processes regulating groundwater quality in a coastal region, Barka, Sultanate of Oman. The rapid urban developments in Barka cause depletion of groundwater quantity and deterioration of quality through excessive consumption and influx of pollutants from natural and anthropogenic activities. In this study, 111 groundwater samples were collected from 79 wells and analysed for pH, EC, DO, temperature, major ions, silica and nutrients. In Barka, water chemistry shows large variation in major ion concentrations and in electrical conductivity, and implies the influence of distinguished contamination sources and hydrogeochemical processes. The groundwater chemistry in Barka is principally regulated by saline sources, reverse ion exchange, anthropogenic pollutants and mineral dissolution/precipitation reactions. Due to ubiquitous pollutants and processes, groundwater samples were classified into two groups based on electrical conductivity. In group1, water chemistry is greatly influenced by mineral dissolution/precipitation process and lateral recharge from upstream region (Jabal Al-Akdar and Nakhal mountains). In group 2, the water chemistry is affected by saline water intrusion, sea spray, reverse ion exchange and anthropogenic pollutants. Besides, high nitrate concentrations, especially in group 2 samples, firm evidence for impact of anthropogenic activities on groundwater quality, and nitrate can be originated by the effluents recharge from surface contamination sources. Ionic ratios such as SO₄/Cl, alkalinity/Cl and total cation/Cl indicate that effluents recharged from septic tank, waste dumping sites and irrigation return flow induce dissolution of carbonate minerals, and enhances solute load in groundwater. The chemical constituents originating from saline water sources, reverse ion exchange and mineral dissolution are successfully differentiated using ionic delta, the difference between the actual concentration of each constituent and its theoretical concentration for a freshwater–seawater mix calculated from the chloride concentration of the sample, and proved that this approach is a promising tool to identify and differentiate the geochemical processes in coastal region. Hence, both regular geochemical methods and ionic delta ensured that groundwater quality in Barka is impaired by natural and human activities.     

Using 87Sr/86Sr, δ18O and δ2H isotopes along with major chemical composition to assess groundwater salinization in lower Shire valley,Malawi

Groundwater resources in some parts of the lower section of Shire River valley, Malawi, are not useable for rural domestic water supply due to high salinity. In this study, a combined assessment of isotopic (⁸⁷Sr/⁸⁶Sr, δ¹⁸O and δ²H) and major ion composition was conducted in order to identify the hydro-geochemical evolution of the groundwater and thereby the causes of salinity. Three major end-members (representing fresh- and saline groundwater, and evaporated recharge) were identified based on major ion and isotopic composition. The saline groundwater is inferred to result from dissolution of evaporitic salts (halite) and the fresh groundwater shows influence of silicate weathering. Conservative mixing models show that brackish groundwater samples result from a three component mixture comprising the identified end-members. Hence their salinity is interpreted to result from mixing of fresh groundwater with evaporated recharge and saline groundwater. On the other hand, the groundwater with low TDS, found at some distance from areas of high salinity, is influenced by mixing of evaporated recharge and fresh groundwater only. Close to the Shire marshes, where there is shallow groundwater, composition of stable isotopes of water indicates that evaporation may also be an important factor.     

Delineation of groundwater salinization in a coastal aquifer, Bousheher, South of Iran

The geochemical processes controlling chemical composition of groundwater are studied using hydrochemical and isotopic data in Abdan-Dayer coastal plain, south of Iran. The salinity of groundwater in the coastal plain ranges from 1,000, a fresh end-member, to more than 50,000 μS cm^?1, a saline end-member. Groundwater salinity increases from the recharge area toward areas with a shallow water table close to the Persian Gulf coast due to direct evaporation and sea water intrusion as confirmed by mixing binary diagrams, stable isotope content, and Br^?/Cl^? ratio. Groundwater flow pattern in the study area has been modified due to over-pumping of groundwater in recent years which resulted in further saline water migration toward fresh water and their mixing. The maximum mixing ratio is estimated about 15% in different parts of the study area according to chloride concentration.     

Hydrogeochemical conditions and evolution at the Äspö HRL,Sweden

The overall hydrogeochemical conditions at and in the near vicinity of the underground experimental Äspö Hard Rock Laboratory (HRL) in SE Sweden have been investigated. Groundwater data from more than 400 samples have been compiled and evaluated. The groundwater samples represent depths down to 1700 m below sea level and sampling has been performed prior to and during the HRL tunnel excavation. Episodic events have to a great extent influenced the hydrochemical evolution since the last glaciation which ended some 13 ka ago. At that time glacial melt water was flushed under hydraulic pressure down into the fracture system to a depth of at least several hundred metres. The next episodic event took place when the Baltic freshwater lake transformed into the brackish Litorina Sea some 7 ka ago. At this time Äspö was covered by the sea and these denser, more saline waters partly replaced the glacial water down to a depth where the density equilibrated with the replacement sea water. At some time around 3–4 ka ago, Äspö started to rise above sea level and meteoric water began to infiltrate the rock.The overall trend of increasing salinity with depth may easily be misinterpreted as a fairly simple groundwater system, evolving from a two component evolution path between non-saline and saline groundwaters. However, when combining the results from environmental isotopes and the chemical parameters using a new modelling tool named M3 (Multivariate Mixing and Mass balance calculations), a higher resolution was obtained and a more complex groundwater pattern, which reflects the present and paleo-hydrogeological events, can be recognised.The measured groundwater composition was modelled to be a mixture of meteoric, past and present Baltic seawater, glacial (or cold climate recharge) and brine type of waters. The modelling result shows that the processes considered to have a dominating impact on the present Äspö groundwater chemistry are mixing, both in disturbed and undisturbed systems, calcite dissolution and precipitation, redox reactions and biological processes. The undisturbed groundwater conditions prior to the HRL tunnel construction at Äspö consisted of:

• 1.A dominating proportion of meteoric fresh water in the upper 250 m of the aquifer.
• 2.A brackish–saline water consisting of mixing proportions of present and ancient Baltic Sea water and glacial melt water present to a depth of 250–600 m.
• 3.Saline water still containing proportions of glacial water which could represent even older glaciations, and brines, a large portion of which have been stagnant for perhaps millions of years, below a depth of 600 m.

During the HRL tunnel construction there were changes in the composition of the water flowing into the tunnel at different locations. Although the variation in salinity was relatively small, the variations in the mixing proportions of the different water types were substantial.     

环境同位素特征对滨海岩溶地区海水入侵过程的指示意义

大连大魏家水源地位于中国北方典型滨海岩溶地区。近30年来,地下淡水的不合理开采造成的地下水位降落漏斗引发了严重的海水入侵。以大魏家水源地为研究对象,通过大量的水文地质调查和水化学及同位素采样测试分析,探讨海水入侵形成的水动力条件,通过分析滨海岩溶含水层中地下水主要水化学和多种同位素(δ2H-δ18O,δ34S,δ13C)组成特征,识别了海水入侵过程中发生的主要水文地球化学作用,并对其进行了定量模拟,从而阐明了岩溶含水层中的海水入侵机理。研究结果表明:大连大魏家海水入侵主要通道为大魏家地区存在的导水断裂、岩溶裂隙以及第四系松散地层。对δ2H-δ18O同位素的组成分析表明,研究区地下水主要来自大气降水补给,结合Cl-浓度分布,认为除海水入侵淡水含水层后增加了地下水中的盐分外,浅层地下水的蒸发也对地下水中盐分的累积起到了重要作用。根据不同水体中δ34SSO4,δ13CHCO3等同位素特征,结合水化学成分(如SO2-4,Cl-)分析认为,研究区微咸水和咸水并不是地下水淡水和海水简单混合而成。利用反向水文地球化学模拟揭示了控制滨海岩溶含水层中水化学演化的主要水文地球化学反应有方解石、蒙脱石和石膏的溶解作用,伊利石的沉淀作用以及Ca-Na离子交换作用,伴随着CO2的释放。     

Saltwater intrusion and nitrate pollution in the coastal aquifer of Dar es Salaam, Tanzania

Dar es Salaam Quaternary coastal aquifer is a major source of water supply in Dar es Salaam City used for domestic, agricultural, and industrial uses. However, groundwater overdraft and contamination are the major problems affecting the aquifer system. This study aims to define the principal hydrogeochemical processes controlling groundwater quality in the coastal strip of Dar es Salaam and to investigate whether the threats of seawater intrusion and pollution are influencing groundwater quality. Major cations and anions analysed in 134 groundwater samples reveal that groundwater is mainly affected by four factors: dissolution of calcite and dolomite, weathering of silicate minerals, seawater intrusion due to aquifer overexploitation, and nitrate pollution mainly caused by the use of pit latrines and septic tanks. High enrichment of Na⁺ and Cl^? near the coast gives an indication of seawater intrusion into the aquifer as also supported from the Na–Cl signature on the Piper diagram. The boreholes close to the coast have much higher Na/Cl molar ratios than the boreholes located further inland. The dissolution of calcite and dolomite in recharge areas results in Ca–HCO₃ and Ca–Mg–HCO₃ groundwater types. Further along flow paths, Ca²⁺ and Na⁺ ion exchange causes groundwater evolution to Na–HCO₃ type. From the PHREEQC simulation model, it appears that groundwater is undersaturated to slightly oversaturated with respect to the calcite and dolomite minerals. The results of this study provide important information required for the protection of the aquifer system.     

The Hydrogeochemistry Of Fractured Plutonic Rocks In The Canadian Shield

The composition of groundwater has been determined in selected granitic, gabbroic and gneissic plutons in the Canadian Shield as part of the Canadian Nuclear Fuel Waste Management Program. A similar geochemical evolution of the groundwater is seen with increasing depth or with flow along the hydraulic gradient, irrespective of rock type. This pattern is comparable to that seen in mine groundwaters from throughout the Canadian Shield. Near-surface groundwaters are typically dilute, slightly alkaline and Ca-(Na)-HCO₃ in composition. They evolve to higher pH, Na-(Ca)-HCO₃ compositions along the flow path because of interaction with plagioclase, calcite precipitation and ion exchange on clay minerals. At greater depths (>≈200 m), groundwater salinity increases as a result of the dissolution of Cl-rich salts in the rock matrix and, in certain areas, mixing with Na-Cl brines from seawater or basinal formation water. Stable and radioactive isotopic data for the groundwaters help to interpret these characteristics and indicate high residence times for the deeper, saline groundwater.

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3 évoluent du fait des interactions avec les plagioclases, de la précipitation de la calcite et des échanges d'ions avec les argiles. Aux plus grandes profondeurs (>≈200 m), l'accroissement de la salinité de l'eau souterraine est provoqué par la dissolution de chlorures de la matrice et, en certains endroits, par le mélange avec des saumures à Na et Cl d'eau de mer ou d'eau de formation de bassin. Les données des isotopes stables et radioactifs des eaux souterraines aident à interpréter leurs caractéristiques; elles indiquent des temps de séjour longs pour les eaux souterraines salées, les plus profondes.

     

Origin of groundwater salinity (current seawater vs. saline deep water) in a coastal karst aquifer based on Sr and Cl isotopes. Case study of the La Clape massif (southern France)

In this study a typical coastal karst aquifer, developed in lower Cretaceous limestones, on the western Mediterranean seashore (La Clape massif, southern France) was investigated. A combination of geochemical and isotopic approaches was used to investigate the origin of salinity in the aquifer. Water samples were collected between 2009 and 2011. Three groundwater groups (A, B and C) were identified based on the hydrogeological setting and on the Cl⁻ concentrations. Average and maximum Cl⁻ concentrations in the recharge waters were calculated (Cl_Ref. and Cl_Ref.Max) to be 0.51 and 2.85 mmol/L, respectively). Group A includes spring waters with Cl⁻ concentrations that are within the same order of magnitude as the Cl_Ref concentration. Group B includes groundwater with Cl⁻ concentrations that range between the Cl_Ref and Cl_Ref.Max concentrations. Group C includes brackish groundwater with Cl⁻ concentrations that are significantly greater than the Cl_Ref.Max concentration. Overall, the chemistry of the La Clape groundwater evolves from dominantly Ca–HCO₃ to NaCl type. On binary diagrams of the major ions vs. Cl, most of the La Clape waters plot along mixing lines. The mixing end-members include spring waters and a saline component (current seawater or fossil saline water). Based on the Br/Cl_molar ratio, the hypothesis of halite dissolution from Triassic evaporites is rejected to explain the origin of salinity in the brackish groundwater.Groundwaters display ⁸⁷Sr/⁸⁶Sr ratios intermediate between those of the limestone aquifer matrix and current Mediterranean seawater. On a Sr mixing diagram, most of the La Clape waters plot on a mixing line. The end-members include the La Clape spring waters and saline waters, which are similar to the deep geothermal waters that were identified at the nearby Balaruc site. The ³⁶Cl/Cl ratios of a few groundwater samples from group C are in agreement with the mixing hypothesis of local recharge water with deep saline water at secular equilibrium within a carbonate matrix. Finally, PHREEQC modelling was run based on calcite dissolution in an open system prior to mixing with the Balaruc type saline waters. Modelled data are consistent with the observed data that were obtained from the group C groundwater. Based on several tracers (i.e. concentrations and isotopic compositions of Cl and Sr), calculated ratios of deep saline water in the mixture are coherent and range from 3% to 16% and 0% to 3% for groundwater of groups C and B, respectively.With regard to the La Clape karst aquifer, the extension of a lithospheric fault in the study area may favour the rise of deep saline water. Such rises occur at the nearby geothermal Balaruc site along another lithospheric fault. At the regional scale, several coastal karst aquifers are located along the Gulf of Lion and occur in Mezosoic limestones of similar ages. The ⁸⁷Sr/⁸⁶Sr ratios of these aquifers tend toward values of 0.708557, which suggests a general mixing process of shallow karst waters with deep saline fossil waters. The occurrence of these fossil saline waters may be related to the introduction of seawater during and after the Flandrian transgression, when the highly karstified massifs invaded by seawater, formed islands and peninsulas along the Mediterranean coast.     

Hydrochemistry in coastal aquifer of southwest Bangladesh: origin of salinity

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.     

Identification of probable groundwater paths in the Amargosa Desert vicinity

In this study, the hydrogeochemical program PHREEQC was used to determine the chemical speciation and mineral saturation indices (SIs) of groundwater in the vicinity of the proposed high-level nuclear waste repository at Yucca Mountain, Nevada (USA). In turn, these data were used to interpret the origin and recharge mode of groundwater, to elucidate the mechanisms of flow and transport, and to determine potential sources of groundwater contamination. PHREEQC was run to determine aqueous dissolved species and minerals that would be in equilibrium with the study area’s groundwater. Selected major ions, associated SI, F⁻ and Ca/Na ion exchange were then examined using the multivariate statistical methods of principal component factor analysis and k-means cluster analysis. Analysis of dissolved ion concentrations, SIs, and Ca/Na ion exchange allows simultaneous consideration of arithmetic (raw concentrations) and logarithmic (SI, ion exchange) variables that describe the hydrochemical system and, therefore, can provide further insight into the system’s behavior. The analysis indicates that the dominant processes and reactions responsible for the hydrochemical evolution in the system are (1) evaporative concentration prior to infiltration, (2) carbonate equilibrium, (3) silicate weathering reactions, (4) limited mixing with saline water, (5) dissolution/precipitation of calcite, dolomite and fluorite, and (6) ion exchange. Principal component factor analysis and k-means cluster analysis of factor scores allow the reduction of dimensions describing the system and the identification of hydrogeochemical facies and the processes that defined and govern their evolution.Statistical analysis results indicate that the northern, west face and southern Yucca Mountain groundwater is fresh water with low concentrations of Ca²⁺, Mg²⁺, Cl⁻, Ca²⁺/(Na⁺)², and CaF₂. The Fortymile Wash groundwater is dilute. The carbonate signature is shown in the Ash Meadows and Death Valley waters with high fluorite SI. Finally, the Crater Flat, Stripped Hills, and Skeleton Hills are dominated by Ca/Na ion exchange, Mg and Ca. The hydrochemical and statistical analyses showed three main groundwater signatures or hydrochemical processes indicating groundwater evolution, potential flowpaths, and recharge areas. The flowpaths are the trace of the Amargosa River, the trace of Fortymile Wash, and its convergence with the Amargosa River. This appears to represent not just a groundwater flow path, but traces of surface runoff infiltration as well.     

Hydrochemical changes in a small tropical island’s aquifer: Manukan Island, Sabah, Malaysia

Small islands groundwater are often exposed to heavy pumpings as a result of high demand for freshwater consumption. Intensive exploitation of groundwater from Manukan Island’s aquifer has disturbed the natural equilibrium between fresh and saline water, and has resulted increase the groundwater salinity and leap to the hydrochemical complexities of freshwater–seawater contact. An attempt was made to identify the hydrochemical processes that accompany current intrusion of seawater using ionic changes and saturation indices. It was observed that the mixing between freshwater–seawater created diversity in geochemical processes of the Manukan Island’s aquifer and altered the freshwater and seawater mixture away from the theoretical composition line. This explained the most visible processes taking place during the displacement.     

唐山曹妃甸浅层水咸化机制及反向模拟

采集了唐海至渤海湾剖面的13组水样,分析了研究区浅层地下水的化学特征及成因机制.运用Phreeqc软件反向模拟了地下水流路径上浅层微咸水(咸水)的补给机理及咸化过程.结果显示:浅层地下水由北向南,ρ(TDS)由0.36 g/L逐渐上升到39.2 g/L,水化学类型从HCO3·Cl-Ca·Mg·Na型过渡为Cl· HCO3-Na型再转变为Cl-Na· Mg型.微咸水形成以咸淡混合为主,期间伴随着岩盐、斜长石、CO2、高岭石、钾长石、石膏的溶解及钙蒙脱石、方解石的沉淀析出.咸水形成初期主要受海水入侵影响,后期受蒸发作用影响又进一步咸化.     

Effect of saline water bodies on the hydrogeochemical evaluation of groundwater at Kalpakkam coastal site, Tamil Nadu

Geochemical signatures of groundwater in Kalpakkam plant site were used to identify the geochemistry of the unconfined coastal aquifer. Ground water samples collected from 14 borewells around the study area were studied for four different seasons viz. Summer, South-west monsoon, North-east monsoon and Post-monsoon to identify the major geochemical processes activated in the study area. Data obtained through chemical analyses of groundwater samples were used for graphical plots and geochemical calculations. Piper, Chloro alkaline indices and Chadda’s diagram were determined for geochemical classification of the groundwaters. Identified geochemical processes were verified and quantified using hydrogeochemical aqueous speciation model, PHREEQC to find out the Saturation Indices (SI) of the possible minerals of the study area. It was observed that majority of the bore well samples were under saturated with respect to minerals such as Gypsum, Aragonite and oversaturated with respect to dolomite and calcite. Parameters such as ion exchange and reverse ion exchange, saline water incursion were observed due to the presence of saline water bodies in addition to dissolution of minerals.     

Groundwater resource sustainability in the Wadi Watir delta, Gulf of Aqaba, Sinai, Egypt

The Wadi Watir delta, in the arid Sinai Peninsula, Egypt, contains an alluvial aquifer underlain by impermeable Precambrian basement rock. The scarcity of rainfall during the last decade, combined with high pumping rates, resulted in degradation of water quality in the main supply wells along the mountain front, which has resulted in reduced groundwater pumping. Additionally, seawater intrusion along the coast has increased salinity in some wells. A three-dimensional (3D) groundwater flow model (MODFLOW) was calibrated using groundwater-level changes and pumping rates from 1982 to 2009; the groundwater recharge rate was estimated to be 1.58?×?10⁶ m³/year. A variable-density flow model (SEAWAT) was used to evaluate seawater intrusion for different pumping rates and well-field locations. Water chemistry and stable isotope data were used to calculate seawater mixing with groundwater along the coast. Geochemical modeling (NETPATH) determined the sources and mixing of different groundwaters from the mountainous recharge areas and within the delta aquifers; results showed that the groundwater salinity is controlled by dissolution of minerals and salts in the aquifers along flow paths and mixing of chemically different waters, including upwelling of saline groundwater and seawater intrusion. Future groundwater pumping must be closely monitored to limit these effects.