A Geochemical Approach to Determine Sources and Movement of Saline Groundwater in a Coastal Aquifer

Geochemical evaluation of the sources and movement of saline groundwater in coastal aquifers can aid in the initial mapping of the subsurface when geological information is unavailable. Chloride concentrations of groundwater in a coastal aquifer near San Diego, California, range from about 57 to 39,400 mg/L. On the basis of relative proportions of major‐ions, the chemical composition is classified as Na‐Ca‐Cl‐SO₄, Na‐Cl, or Na‐Ca‐Cl type water. δ²H and δ¹⁸O values range from ?47.7‰ to ?12.8‰ and from ?7.0‰ to ?1.2‰, respectively. The isotopically depleted groundwater occurs in the deeper part of the coastal aquifer, and the isotopically enriched groundwater occurs in zones of sea water intrusion. ⁸⁷Sr/⁸⁶Sr ratios range from about 0.7050 to 0.7090, and differ between shallower and deeper flow paths in the coastal aquifer. ³H and ¹⁴C analyses indicate that most of the groundwater was recharged many thousands of years ago. The analysis of multiple chemical and isotopic tracers indicates that the sources and movement of saline groundwater in the San Diego coastal aquifer are dominated by: (1) recharge of local precipitation in relatively shallow parts of the flow system; (2) regional flow of recharge of higher‐elevation precipitation along deep flow paths that freshen a previously saline aquifer; and (3) intrusion of sea water that entered the aquifer primarily during premodern times. Two northwest‐to‐southeast trending sections show the spatial distribution of the different geochemical groups and suggest the subsurface in the coastal aquifer can be separated into two predominant hydrostratigraphic layers.     

Hydrochemical Analyses and Evaluation of Groundwater Resources of North Jordan

The hydrochemical analyses of twenty-three springs were used to determine the properties and types of groundwater of the Tertiary-Quaternary Aquifer of northern Jordan. The result shows that the geological formation influences the quality of the investigated groundwater more than the anthropogenic factors. The water of the Quaternary-Tertiary aquifer is enriched in Ca⁺⁺ due to the dissolution of the nearby carbonate rocks. The investigated water has a low EC values with Ca(Na)-HCO₃ water type. Most springs belong to this hydrochemical facies except Malka. Groundwater in the Malka wells has high salinity with NaCl waters and a strong Ca(Mg)-HCO₃ facies (900 to 1000 mg/l TDS). The area long-term hydrochemical data have been also evaluated; general trend of increase of the analyzed ion was observed. Bicarbonate represents the most abundant anion in the studied water, which exceeds the permissible limits. Nitrates (NO ₃ ^? ) also exceed the permissible limit and are the most common contaminant in the investigated water. Data on dissolved major and trace elements (K⁺, Na⁺, Mg²⁺, Ca²⁺, Cl^?, SO ₄ ^2? , Fe, Zn, Cu and Pb) in the investigated water revealed that the concentrations lie within the natural background range. The positive correlation values between various ions indicate that most of ions come from same lithological sources. According to the residual sodium carbonate, and EC values, the studied springs are suitable for agricultural purposes.     

Origin and chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta,Botswana

The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ¹⁸O and δ¹³C_DIC). The δD and δ¹⁸O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO₃ type and the deep (≥10 m) groundwater is Na–K–HCO₃ to HCO₃–Cl–SO₄ to Cl–SO₄–HCO₃. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ¹³C_DIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.     

Risk assessment and ranking of heavy metals concentration in Iran’s Rayen groundwater basin using linear assignment method

Groundwater is an important source of freshwater for domestic, agricultural and industrial uses in Iran. Groundwater quality assessment and environmental evaluation are considered as critical issues in recent years. Intensive human activities have resulted in significant changes in environment leading to serious groundwater contamination. This research proposes a two-part systematic approach to tackle heavy metals contamination problem in Rayen Basin (southeast Iran). The first part consists of determining geochemical characteristics and evaluating groundwater quality through application of water quality index and heavy metal pollution indices (i.e. HPI and MI). The second part includes ranking sampling stations based on heavy metals concentration in groundwater using linear assignment method. Six types of water could be identified according to the dominant cations and anions in samples: Ca–HCO₃, Ca–SO₄, Na–Cl, Na–HCO₃, Na–SO₄ and mixed water type. Calculation of indices revealed that natural and anthropogenic activities are playing a vital role in degrading groundwater quality in the study area. The proposed methodology can help in groundwater resource management and preventative activities by identifying risk factors and recognizing their pollution level. The results of this research provide useful and effective information for water pollution control and management and can be used in environmental studies in order to protect groundwater resources in the future.     

The impact of freshwater and wastewater irrigation on the chemistry of shallow groundwater: a case study from the Israeli Coastal Aquifer

Differences in the impact of irrigation with freshwater versus wastewater on the underlying shallow groundwater quality were investigated in the Coastal Aquifer of Israel. Seven research boreholes were drilled to the top-most 3–5 m of the saturated zone (the water table region-WTR) in the agricultural fields. The unsaturated zone and the WTR below the irrigated fields consist mainly of clayey sands, while the main aquifer comprises mainly of calcareous sandstones and sands. We show that the salinity and composition of the groundwater at the WTR are highly variable over a distance of less than 1 km and are controlled by the irrigating water and the processes in the overlying unsaturated zone. Tritium data in this groundwater (4.6 tritium units (TU)) support that these water are modern recharge. The water at the WTR is more saline and has a different chemical composition relative to the overlying irrigation water. High SAR values (sodium adsorption ratio) in wastewater irrigation lead to absorption of Na⁺ onto the clay and release of Ca²⁺ into the recharging water, resulting in low Na/Cl (0.4 compared to 1.2 in the wastewater) and high Ca/Cl ratios. In contrast, in the freshwater-irrigated field the irrigation water pumped from the aquifer (Na/Cl=0.9; SAR=0.6) is modified into Na-rich groundwater (Na/Cl=2.0) due to reverse base-exchange reactions. The high NO₃ concentration (>100 mg/l) in the WTR below both fields is derived from the agricultural activities. In the freshwater field, the source of NO₃ is fertilizer leachates, whereas in the wastewater field, where less fertilizers are applied, nitrate is probably derived from nitrification of the NH₄ in the wastewater. Some of the original inorganic nitrogen in the wastewater is consumed by the agricultural plants, resulting in a lower inorganic-N/Cl ratio in the WTR as compared to that in the wastewater. This study demonstrates the important role of the composition of irrigation water, combined with lithology and land use, in determining the quality of the water that recharge the aquifer below agricultural fields.     

Evaluation of groundwater hydrochemical characteristics and mixing behavior in the Daying and Qicun geothermal systems,Xinzhou Basin

This paper examines groundwater hydrochemical characteristics during mixing between thermal and non-thermal groundwater in low-to-medium temperature geothermal fields. A case study is made of Daying and Qicun geothermal fields in the Xinzhou basin of Shanxi province, China. The two geothermal fields have similar flow patterns, with recharge sourced from precipitation in mountain areas heated through a deep cycle, before flowing into overlying Quaternary porous aquifers via fractures. Hydrochemical features of 60 ground- and surface water samples were examined in the context of hydrogeologic information. The average temperatures of the deep geothermal reservoirs are estimated to be 125 °C in Daying field, and 159 °C in Qicun field, based on Na–K–Mg geothermometry, while slightly lower estimates are obtained using silica geothermometers. Hydrochemical features of thermal water are distinct from cold water. Thermal groundwater is mainly Cl·SO₄–Na type, with high TDS, while non-thermal groundwater is mostly HCO₃–Ca·Mg and HCO₃–Ca type in the Daying and Qicun regions, respectively. Hydrogeochemical processes are characterized by analyzing ion ratios in various waters. Higher contents of some minor elements in thermal waters, such as F, Si, B and Sr, are probably derived from extended water–rock interaction, and these elements can be regarded as indicators of flow paths and residence times. Mixing ratios between cold and thermal waters were estimated with Cl, Na, and B concentrations, using a mass balance approach. Mixing between ascending thermal waters and overlying cold waters is extensive. The proportion of water in the Quaternary aquifer derived from a deep thermal source is lower in Daying geothermal field than in Qicun field (5.3–7.3% vs. 6.3–49.3%). Mixing between thermal and non-thermal groundwater has been accelerated by groundwater exploitation practices and is enhanced near faults. Shallow groundwater composition has also been affected by irrigation with low-temperature thermal water.     

Ground-Water Chemistry of Dibdiba Formation, North Kuwait

Chemical studies have been carried out on a number of water wells from the Dibdiba Formation northeast of Kuwait. Water salinity of this formation ranges between 3,300 mg/l to 7,000 mg/l, increasing with depth. The water entrapped in Dibdiba Formation is mainly sodium chloride type which can be differentiated into three different groups according to the ranges of concentration of the main cations and anions. These groups are: (3331113) sodium chloride water type in which Cl > Na, group (3333113) sodium chloride water type in which Na > Cl. In both groups the sequence of dominant cations is Na > Ca > Mg. Group (3333111) sodium chloride water type has Na > Cl and the sequence of dominant cations is Na > Mg > Ca. Chemical ratios of Ca/Mg, Na/Cl, and C1/HCO₃ were worked out for Dibdiba ground water. The ratio of Ca/Mg Dibdiba Formation ranges from 0.4 to 8.58, the ratio of Na/Cl ranges between 0.98 to 1.33, and the ratio of C1/HCO₃ is 232. A plot of chemical analysis on a trilinear diagram shows that Dibdiba Formation ground-water chemical properties are dominated by alkalies (Na > Ca) and strong acid (Cl > SO₄). Water chemistry may reflect the history of the flow path, indicating regional flow as shown by increasing Na⁺, Cl^-, SO^–₄ and where Ca⁺, Mg⁺ achieve equilibrium.     

Separating baseline conditions from anthropogenic impacts: example of the Damour coastal aquifer (Lebanon)

Abstract

A new structured approach is presented to derive groundwater baseline conditions, in this case for a dolomitic limestone aquifer suffering from salinization and other anthropogenic impacts. It builds on the HydroChemical System Analysis (HCSA) to map different groundwater bodies (hydrosomes) and hydrochemical zones within them, each of which show significant differences in baseline conditions. It also comprises a rigorous elimination scheme for samples affected by bias or pollution. The method is applied to the Damour coastal aquifer system, south of Beirut (Lebanon). Concentrations of Cl, Cl/Br, ²H, ¹⁸O and Ca/Sr were used to discern five hydrosomes and to determine mixing ratios. The dominant hydrochemical facies was (sub)oxic, calcareous and salinized, indicating a very low reduction capacity of the aquifer system, strong dissolution of dolomitic limestone and clear traces of seawater encroachment. The method proposed was capable of filtering out baseline conditions for 16 main constituents, 64 trace elements and two isotopes.     

Using hydrochemical tracers to assess impacts of unsewered urban catchments on hydrochemistry and nutrients in groundwater

We applied graphical methods and multivariate statistics to understand impacts of an unsewered slum catchment on nutrients and hydrochemistry of groundwater in Kampala, Uganda. Data were collected from 56 springs (groundwater), 22 surface water sites and 13 rain samples. Groundwater was acidic and dominated by Na, Cl and NO₃. These ions were strongly correlated, indicating pollution originating from wastewater infiltration from on‐site sanitation systems. Results also showed that rain, which was acidic, impacted on groundwater chemistry. Using Q‐mode hierarchical cluster analysis, we identified three distinct water quality groups. The first group had springs dominated by Ca‐Cl‐NO₃, low values of electrical conductivity (EC), pH and cations, and relatively high NO₃ values. These springs were shown to have originated from the acidic rains because their chemistry closely corresponded to ion concentrations that would occur from rainfall recharge, which was around 3.3 times concentrated by evaporation. The second group had springs dominated by Na‐K‐Cl‐NO₃ and Ca‐Cl‐NO₃, low pH but with higher values of EC, NO₃ and cations. We interpreted these as groundwater affected by both acid rain and infiltration of wastewater from urban areas. The third group had the highest EC values (average of 688 μS/cm), low pH and very high concentrations of NO₃ (average of 2.15 mmol/l) and cations. Since these springs were all located in slum areas, we interpreted them as groundwater affected by infiltration of wastewater from poorly sanitized slums areas. Surface water was slightly reducing and eutrophic because of wastewater effluents, but the contribution of groundwater to nutrients in surface water was minimal because o‐PO₄ was absent, whereas NO₃ was lost by denitification. Our findings suggest that groundwater chemistry in the catchment is strongly influenced by anthropogenic inputs derived from nitrogen‐containing rains and domestic wastewater. Copyright © 2013 John Wiley & Sons, Ltd.     

Hydrogeochemical characteristics of surface water and groundwater in the karst basin,southwest China

Groundwater is a very significant water source used for irrigation and drinking purposes in the karst region, and therefore understanding the hydrogeochemistry of karst water is extremely important. Surface water and groundwater were collected, and major chemical compositions and environmental isotopes in the water were measured in order to reveal the geochemical processes affecting water quality in the Gaoping karst basin, southwest China. Dominated by Ca²⁺, Mg²⁺, HCO₃^? and SO₄^2?, the groundwater is typically characterized by Ca? Mg? HCO₃ type in a shallow aquifer, and Ca? Mg? SO₄ type in a deeper aquifer. Dissolution of dolomite aquifer with gypsiferous rocks and dedolomitization in karst aquifers are important processes for chemical compositions of water in the study basin, and produce water with increased Mg²⁺, Ca²⁺ and SO₄^2? concentrations, and also increased TDS in surface water and groundwater. Mg²⁺/Ca²⁺ molar ratios in groundwater decrease slightly due to dedolomitization, while the mixing of discharge of groundwater with high Mg²⁺/Ca²⁺ ratios may be responsible for Mg²⁺/Ca²⁺ ratios obviously increasing in surface water, and Mg²⁺/Ca²⁺ ratios in both surface water and groundwater finally tending to a constant. In combination with environmental isotopic analyses, the major mechanism responsible for the water chemistry and its geochemical evolution in the study basin can be revealed as being mainly from the water–rock interaction in karst aquifers, the agricultural irrigation and its infiltration, the mixing of surface water and groundwater and the water movement along faults and joints in the karst basin. Copyright © 2009 John Wiley & Sons, Ltd.     

Using principal component analysis in the investigation of groundwater hydrochemistry of Upper Jezireh Basin,Syria

Principal component analysis (PCA) was applied to hydrochemical and isotopic data of 34 groundwater samples. This allowed the reduction of 20 variables to four significant PCs that explain 81.9% of the total variance; F1 (47.1%) explains the groundwater mineralization, whereas F2 (17%) shows isotopic enrichment and nitrate pollution. Based on an iso-factor scores map of F1, three water zones were delineated: Zone A (F1 < ?1), with fresh groundwater from the unconfined aquifer; Zone B (1 > F1 > ?1), with moderate mineralization from the confined–unconfined aquifer boundary; and Zone C (F1 > 1), with the most mineralized hot water from the confined aquifer. The iso-factor scores map of F2 delineates positive values representing samples from the unconfined aquifer, with freshwater and nitrate contamination associated with stable isotope enrichment, whereas negative values represent samples from the confined aquifer. The results clearly demonstrate the usefulness of PCA in groundwater hydrochemistry investigations.     

Exploring Groundwater Resources and Recharge Potentialities at El-Gallaba Plain,Western Desert,Egypt

Egypt has a fast-growing population rate of 2.5%/year; consequently, there is an increase in the water demand for living and launching different development plans. Meanwhile, there is intensive construction of several dams in the upstream Nile basin countries. Thus, it is necessary to search for new water resources to overcome the expected shortages of the Nile water supply by focusing on alternative groundwater resources. El-Gallaba Plain area is one of the most promising areas in the western desert of Egypt attaining the priority for new reclamation projects; however, its hydrogeological setting is not well understood. The present work aims at identifying the recharge potential of the groundwater aquifers in El-Gallaba Plain, as well as exploring the role of geologic structures as natural conduits, and evaluating the groundwater types, origin and distribution. The integration of hydrogeophysical studies (aero and land magnetic surveys, vertical electrical sounding), hydrochemical analyses and remote sensing were successfully used for assessing the groundwater development potential. The hydrogeophysical studies show a large graben bound aquifer with thickness exceeding 220 m. The hydrochemical results indicate the presence of three major water types; Na mix, Na Cl, Na Cl HCO₃ with salinities ranging between 227 and 4324 mg/L. The aquifer receives little recharge from the western fractured calcareous plateau from past pluvial periods and scarce present flashfloods. There is no indication for recent recharge from Lake Nasser to the aquifer domain. Further modeling studies are essential for establishing sustainable abstraction levels from this aquifer.     

Effects of ultrafiltration on salt migration and isotopic composition of pore water in groundwater depression area in Hengshui,NCP

Clay aquitards are semipermeable membranes that allow groundwater flow while retarding solute migration has been researched extensively but also subjected to much debate. At present, there is no evidence of whether the physical and chemical properties of clay soil and the isotopic composition of pore water affect the semipermeable membrane effect. In this study, we collected clay samples from drilling cores (30–90 m) in the Hengshui area located in the North China Plain (NCP), then extracted pore water using a high-pressure squeezing device. Vertical hydrochemical and isotopic profile variation trends for the pore water were revealed using hydrochemical (Cl⁻, Na⁺, Ca²⁺, K⁺, Mg²⁺, and SO₄²⁻) and stable isotopic measurements of H, O and Cl. The results showed that the hydrochemical clay interlayer pore water of the saline aquifer is Cl/SO₄-Na/Mg type and the average total dissolved solids (TDS) are 10.17 g/L. However, the hydrochemical clay aquitard pore water is of the Cl/SO₄-Na/Ca type with an average TDS of 1.90 g/L. The hydrochemical clay interlayer pore water of aquifer II is of Cl-Na/Ca type with an average TDS of 1.10 g/L. Our results showed that the water quality of the aquifer II is not affected by the upper part of the saline aquifer, thus the clay aquitard acts as a significant barrier to salt movement. A polarization layer concentrated in ions was formed between the upper part of the saline aquifer and the clay aquitard. The concentration polarization layer increases the salt-inhibition effect. H, O and Cl isotopic composition results showed significant fractionation. The pore water of aquifer II lacked heavy isotopes (²H, ¹⁸O, ³⁷Cl), but had significant heavy isotope enrichment in the concentrated polarized layer (the δ²H value was −76‰, the δ¹⁸O value was −8.4‰, and the δ³⁷Cl value was 1.59‰). Hyperfiltration thus played a significant role in isotope fractionation.     

Characterization of the groundwater flow regime and hydrochemistry of groundwater from the Buem formation,Eastern Ghana

This study demonstrates the application of multivariate statistical methods in definition of groundwater recharge and discharge areas in a sedimentary basin in Ghana. Q‐mode hierarchical cluster analysis (HCA) was applied to 57 hydrochemical data from the Buem formation in the northern part of the Volta Region in Ghana. R‐mode HCA and R‐mode factor analysis were then applied to the same dataset to reveal the processes controlling the hydrochemistry of groundwater from this hydrogeological formation. Results of both the Q‐ and R‐mode analyses were backed by graphical methods. The analyses revealed two major water types, differentiated by salinity levels into four spatial groundwater associations. The characteristics of the four groundwater types are discussed. The recharge areas are characterized by Ca? HCO₃ low salinity waters which evolve through rock–water interactions to Na? HCO₃ high salinity waters in the discharge areas. This study finds that the hydrochemistry of groundwater from this formation is mainly controlled by the weathering of minerals, principally silicates in the aquifer matrix. The effects of the chemistry of recharging precipitation are higher in the recharge areas, while mineral weathering tends to be severe close to the discharge areas in the groundwater flow regime. All the four spatial groundwater associations have low sodium content, but salinity levels increase towards the discharge areas, such that some of wells in the discharge areas may not be acceptable for irrigation on grounds of high salinities which might affect the osmotic potentials of plants. Copyright © 2011 John Wiley & Sons, Ltd.     

Multivariate statistical analysis and environmental isotopes of Amman/Wadi Sir (B2/A7) groundwater,Yarmouk River Basin,Jordan

Multivariate statistical techniques, cluster and factor analyses were applied on the Amman/Wadi Sir groundwater chemistry, Yarmouk River basin, north Jordan. The main objective was to investigate the main processes affecting the groundwater chemical quality and its evolution. The k‐means cluster analysis yields three groups with distinct ionic concentrations. Cluster 1 comprises the vast majority of the sampled wells, and the water that belongs to this cluster can be classified as freshwater. Cluster 2 comprises only 2% of the sampled wells; it has the highest ionic concentration. The water of this cluster can be classified as brackish water. Cluster 3 involves 23% of the sampled wells, and it has total ionic concentration intermediate to that of clusters 1 and 2. Factor analysis yields a three‐factor model, which explains 76.77% of the groundwater quality variation. Factor 1 ‘salinity factor’ involves EC, Na⁺, Cl^‐, SO₄^‐2, K⁺ and Mg⁺² and reflects groundwater salinization because of overpumping. Factor 2 ‘hardness factor’ includes Ca⁺², HCO₃^‐ and the pH value and signifies soil–water/rock interaction. Factor 3 ‘nitrate factor’ involves only NO₃^‐ and points to groundwater contamination because of human activities, mainly untreated wastewater, and crops and animal cultivation in the unconfined portion of the aquifer. Factors 1 and 3 can be described as human‐induced factors, whereas factor 2 can be described as geogenic factor. Factors' scores were mapped to deduce the controlling processes on the groundwater chemistry. Stable isotope composition of ¹⁸O and ²H has revealed that the groundwater is a mixture of two water types. The radioactive isotopes tritium and ¹⁴ C were used to evaluate present day recharge to the aquifer and to estimate the groundwater age, respectively. Present day recharge to the groundwater is taking place in the unconfined portion of the aquifer as it is indicated by the measurable tritium content and low groundwater age. Copyright © 2012 John Wiley & Sons, Ltd.     

HYDROGEOCHEMISTRY OF GROUNDWATER IN CENTRAL ISRAEL

ABSTRACT

The regional groundwater groups of central Israel include:

1. bicarbonate waters representing the replenishment areas;

2. chloride waters representing the confined and the base-level zones;

3. sulfate waters of the intermediate zones (fig. 2).

These water types were found to fit broadly into five hydrogeographical groups.

The chemical evolution of the ground waters is a function of: a) lithology and solubility of the aquifer components and of the surrounding strata; b) mixing between groundwater bodies of different composition. The first factor is important mainly within the confined zones while the latter is conspicuous in the Rift Valley and adjacent areas.

Groundwater mixing within the Dead Sea basin produces waters with Mg > Na > Ca, and Cl ? SO > HCO₃. Other brines show the order: Ca > Na > Mg. All these brines show compositions different from ocean water.     

Assessment of seasonal groundwater quality and potential saltwater intrusion: a study case in Urmia coastal aquifer (NW Iran) using the groundwater quality index (GQI) and hydrochemical facies evolution diagram (HFE-D)

Coastal aquifers are at threat of salinization in most parts of the world. This work investigated the seasonal hydrochemical evolution of coastal groundwater resources in Urmia plain, NW Iran. Two recently proposed methods have been used to comparison, recognize and understand the temporal and spatial evolution of saltwater intrusion in a coastal alluvial aquifer. The study takes into account that saltwater intrusion is a dynamic process, and that seasonal variations in the balance of the aquifer cause changes in groundwater chemistry. Pattern diagrams, which constitute the outcome of several hydrochemical processes, have traditionally been used to characterize vulnerability to sea/saltwater intrusion. However, the formats of such diagrams do not facilitate the geospatial analysis of groundwater quality, thus limiting the ability of spatio-temporal mapping and monitoring. This deficiency calls for methodologies which can translate information from some diagrams such Piper diagram into a format that can be mapped spatially. Distribution of groundwater chemistry types in Urmia plain based on modified Piper diagram using GQI_Piper(mix) and GQI_Piper(dom) indices that Mixed Ca–Mg–Cl and Ca-HCO₃ are the dominant water types in the wet and dry seasons, respectively. In this study, a groundwater quality index specific to seawater intrusion (GQI_SWI) was used to check its efficiency for the groundwater samples affected by Urmia hypersaline Lake, Iran. Analysis of the main processes, by means of the Hydrochemical Facies Evolution Diagram (HFE-Diagram), provides essential knowledge about the main hydrochemical processes. Subsequently, analysis of the spatial distribution of hydrochemical facies using heatmaps helps to identify the general state of the aquifer with respect to saltwater intrusion during different sampling periods. The HFE-D results appear to be very successful for differentiating variations through time in the salinization processes caused by saltwater intrusion into the aquifer, distinguishing the phase of saltwater intrusion from the phase of recovery, and their respective evolutions. Both GQI and HFE-D methods show that hydrochemical variations can be read in terms of the pattern of saltwater intrusion and groundwater quality status. But generally, in this case (i.e. saltwater and not seawater intrusion) the HFE-D method was presented better efficiency than GQI method (including GQI_Piper and GQI_SWI).     

Hydrogeochemistry of thermal and mineral water springs of the Azores archipelago (Portugal)

Mineral and thermal water chemistry from the Azores archipelago was investigated in order to discriminate among hydrochemical facies and isotopic groups and identify the major geochemical processes that affect water composition. A systematic geochemical survey of mineral and thermal water chemistry was carried out, incorporating new data as well as results from the literature. The Azores are a volcanic archipelago consisting of nine islands and samples were collected at São Miguel, Graciosa, Faial, São Jorge, Pico and Flores islands. Hydrothermal manifestations show the effects of active volcanism on several islands. Discharges are mainly related to active Quaternary central volcanoes, of basaltic to trachytic composition, but also some springs are related to older dormant or extinct volcanoes.Multivariate analysis – principal component and cluster analysis – enables classification of water compositions into 4 groups and interpretation of processes affecting water compositions. Groups 1 and 2 discharge from perched-water bodies, and mostly correspond to Na–HCO₃ and Na–HCO₃–Cl type waters. These groups comprise of cold, thermal (27 °C–75 °C) and boiling waters (92.2 °C–93.2 °C), with a wide TDS range (77.3–27, 145.7 mg/L). Group 3 is made of samples of dominated Na–SO₄ from very acid boiling pools (pH range of 2.02–2.27) which are fed by steam-heated perched-water bodies. Group 4 is representative of springs from the basal aquifer system and corresponds to Na–Cl type fluids, with compositions dominated by seawater.Results are used to further develop a conceptual model characterizing the geochemical evolution of the studied waters. Mineral and thermal waters discharging from perched-water bodies are of meteoric origin and chemically evolve by absorption of magmatic volatiles (CO₂) and by a limited degree of rock leaching. Existing data also suggest mixture between cold waters and thermal water. Water chemistry from springs that discharge from the basal aquifer system evolves by mixing with seawater; although, processes such as absorption of magmatic volatiles (CO₂), rock leaching and mixture with hydrothermal waters are not excluded by the data because the actual composition of these waters deviates from that expected considering only conservative mixing between fresh and seawater.     

Variation of hydrogeochemical characteristics of water in surface flows,shallow wells,and boreholes in the coastal city of Douala (Cameroon)

ABSTRACT

Groundwater is used by 3?million inhabitants in the coastal urban city of Douala, Cameroon, but comprehensive data are too sparse for it to be managed in a sustainable manner. Hence this study aimed to (1) assess the potability of the groundwater; (2) evaluate the spatial variation of groundwater composition; and (3) assess the interaction and recharge mechanisms of different water bodies. Hydrogeochemical tools and methods revealed the following results in the Wouri and Nkappa formations of the Douala basin, which is beneath Douala city: 30% of water samples from hand-dug wells in the shallow Pleistocene alluvium aquifer were saline and highly mineralized. However, water from boreholes in the deeper (49–92 m depth) Palaeocene aquifer was saline-free, less mineralized and potable. Water in the shallow aquifer (0.5–22 m depth) was of Na⁺-K⁺-Cl^?-NO₃^? type and not potable due to point source pollution, whereas Ca⁺-HCO₃^? unpolluted water dominates in the deeper aquifer. Water in the deep and shallow aquifers indicates the results of preferential flow pass and evaporative recharge, respectively. Possible hydrogeochemical processes include point source pollution, reverse ion exchange, remote recharge areas and mixing of waters with different chemical signatures.

EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M.D. Fidelibus     

Hydro-geochemical simulation for the evolution of groundwater quality in Yinchuan Plain,China

ABSTRACT

Water quality in the arid regions has long been an issue of great concern in the world. In this study, quantitative research was carried out to create new knowledge to understand the processes that determine the variation in the groundwater chemical composition of the Yinchuan Plain, China. In this context, the distribution and zonation characteristics of groundwater in this area were assessed using geochemical modelling of groundwater quality evolution. The results show the existence of an obvious zonation from the recharge area to the discharge area in the study area. Dominant anions transform from HCO₃ in the inclined pluvial area to HCO₃·SO₄·Cl in the discharge region, while the main cations vary from Ca and Mg to Na and Mg. The simulation results indicate that the evaporation process triggers 2–35% of groundwater loss, leading to an increase in the total dissolved solids. The irrigation leakage mixes with the groundwater at about 8:2, suggesting that the irrigation leakage dilutes the groundwater.