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.     

Assessment of the factors controlling groundwater quality in a coastal aquifer adjacent to the Bay of Bengal,India

A study has been conducted in the heavily populated coastal areas of the Puri district (Odisha, India) with the aim to: (1) identify the factors that influence the major ion composition and concentrations of trace elements in groundwater; (2) determine the spatial distribution of the water-quality parameters and how they vary on a seasonal basis. To do this, groundwater samples were collected from 60 shallow tube wells located along the Puri coast during the pre-monsoon and post-monsoon seasons. Based on their TDS content, 52% of the collected groundwater samples were identified as being brackish-to-saline and unsuitable for drinking purposes in both the pre- and post-monsoon seasons. Significant concentrations of trace elements including Ba, Br, F, Fe, Mn, and Sr were detected in most of the samples. Iron concentrations were found to be higher than the WHO drinking water guideline value (0.3 mg/l) in 92% of the samples irrespective of seasons. Elevated Mn concentrations were observed in 37% and 40% of samples during the pre-monsoon and post-monsoon seasons, respectively. In addition, fluoride concentrations in excess of the WHO limit (1.5 mg/l) were found in 15% of samples during the pre-monsoon and 23% of samples during the post-monsoon season. The concentrations of major and trace elements show wide spatial and minor temporal variations. Large spatial and limited temporal variations in Cl and Na concentrations along with considerable Br and Sr concentrations in groundwater suggest that saltwater intrusion is the dominant process controlling groundwater quality in the study area, although other processes including ion exchange, the precipitation and dissolution of minerals, microbial activity, and the weathering of aquifer material also play roles to some extent in determining the spatial and seasonal distribution of the major and trace elements in coastal groundwater. Grouping of various water-quality parameters related to these processes by principal component analysis and their linking to one cluster in the hierarchical cluster analysis further supports the view that these processes control the groundwater chemistry in the coastal aquifer.     

Quantification of groundwater–seawater interaction in a coastal sandy aquifer system: a study from Panama,Sri Lanka

The Panama coastal aquifer system is an important water resource in the southeast coast of Sri Lanka that provides adequate supplies of water for agriculture and domestic uses. One of the biggest threats to these fragile aquifers is the sea water intrusion. In this study, recharging mechanism and geochemical evaluation of groundwater in the coastal sandy aquifer of Panama were evaluated using chemical and stable isotope techniques. Thirty groundwater samples were collected and analyzed for their major ion concentrations and stable isotope ratios of oxygen (¹⁸O/¹⁶O) and hydrogen (D/H). All studied samples showed a ranking of major anions in the order Cl^? > HCO ₃ ^?  > SO ₄ ^2?  > N-NO₃ ^? while cations showed a decreasing order of abundance with Na⁺ > Ca²⁺ > Mg²⁺ > K⁺. Dominant groundwater hydrogeochemical types were Na–Cl and mixed Ca–Mg–Cl. Results of saturation index calculations indicate that the investigated groundwater body was mostly saturated with respect to calcite, dolomite and gypsum. In addition, stable isotope and geochemical data suggest that fresh groundwater in the aquifer is recharged mainly by local precipitation with slight modification from evaporation and saline water intrusions. Isotope data suggest that mixing of salt water with freshwater occurs in aquifers which are located towards the lagoon. Since the communities in the study area depend entirely on groundwater, an understanding of the hydrogeochemical characteristics of the aquifer system is extremely important for the better water resource management in the region.     

Geochemistry and assessment of hydrogeochemical processes in groundwater in the southern part of Bathinda district of Punjab, northwest India

Hydrogeochemistry of groundwater is important for sustainable development and effective management of the groundwater resource. Fifty-six groundwater samples were collected from shallow tube wells of the intensively cultivated southern part of district Bathinda of Punjab, India, during pre- and post-monsoon seasons. Conventional graphical plots were used to define the geochemical evaluation of aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. Negative values of chloroalkaline indices suggest the prevalence of reverse ion exchange process irrespective of the seasons. A significant effect of monsoon is observed in terms chemical facies as a considerable amount of area with temporary hardness of Ca²⁺–Mg²⁺–HCO₃ ^? type in the pre-monsoon switched to Ca²⁺–Mg²⁺–Cl^? type (18%) followed by Na⁺–HCO₃ ^? type (14%) in the post-monsoon. Evaporation is the major geochemical process controlling the chemistry of groundwater process in pre-monsoon; however, in post-monsoon ion exchange reaction dominates over evaporation. Carbonate weathering is the major hydrogeochemical process operating in this part of the district, irrespective of the season. The abundance of Ca²⁺ + Mg²⁺ in groundwater of Bathinda can be attributed mainly to gypsum and carbonate weathering. Silicate weathering also occurs in a few samples in the post-monsoon in addition to the carbonate dissolution. Water chemistry is deteriorated by land-use activities, especially irrigation return flow and synthetic fertilisers (urea, gypsum, etc.) as indicted by concentrations of nitrate, sulphate and chlorides. Overall, results indicate that different natural hydrogeochemical processes such as simple dissolution, mixing, weathering of carbonate minerals locally known as ‘‘kankar’’ and silicate weathering are the key factors in both seasons.     

Geochemical Appraisal of Groundwater Quality in Ottapidaram Taluk,Thoothukudi District,Tamil Nadu using Graphical and Numerical Method

Groundwater qualities of coastal aquifers in the Ottapidaram taluk of Thoothukudi district, Tamil Nadu have been extensively monitored in post monsoon seasons in 2014 to assess its suitability in relation to domestic and drinking uses in four regions (N-S-EW). 34 groundwater samples were analyzed for various physicochemical attributes like pH, electrical conductivity (EC), Total dissolved solid (TDS), Na, K, Ca, Mg, Cl, HCO₃, CO₃, SO₄, NO₃, PO₄. Most of these parameters fall under not permissible limits. The western part of the study area is highly polluted from K, Cl, HCO₃ due to industrial/agriculture activity. The southern part is less polluted compared to other region. Hydrogeochemical processes controlling the water chemistry (Gibbs) indicates that most of groundwater samples fall at rock-weathering supremacy zone. Geochemical processes and temporal variation in the groundwater in this area are influenced by evaporation processes, ion exchange and dissolution of minerals. Major cation and anion ionic interaction indicate that weathering reactions have an inconsequential role in the hydrochemical processes of the shallow groundwater system. As a result of the hydrogeochemical analysis, seawater intrusion, aquifer rock weathering, sewer leakage are the overriding factors that determine the major ionic composition. The appropriate management plan is necessary to preserve precious groundwater resources.     

Multivariate statistical analyses of the groundwater system in Darb El-Arbaein, Southwestern Desert, Egypt

In Darb El-Arbaein, the groundwater is the only water resource. The aquifer system starts from Paleozoic–Mesozoic to Upper Cretaceous sandstone rocks. They overlay the basement rocks and the aquifer is confined. In the present research, the performance of the statistical analyses to classify groundwater samples depending on their chemical characters has been tested. The hydrogeological and hydrogeochemical data of 92 groundwater samples were obtained from the General Authority for Rehabilitation Projects and Agricultural Development authority in northern, central, and southern Darb El-Arbaein. A robust classification scheme for partitioning groundwater chemistry into homogeneous groups was an important tool for the characterization of Nubian sandstone aquifer. We test the performance of the many available graphical and statistical methodologies used to classify water samples. R-mode, Q-mode, correlation analysis, and principal component analysis were investigated. All the methods were discussed and compared as to their ability to cluster, ease of use, and ease of interpretation. The correlation investigation clarifies the relationship among the lithologic, hydrogeologic, and anthropogenic factors. Factor investigation revealed three factors, namely, the evaporation process–agricultural impact–lithogenic dissolution, the hydrogeological characteristics of the aquifer system, and the surface meteoric water that recharge the aquifer system. Two main clusters that subdivided into four subclusters were identified in the groundwater system based on hydrogeological and hydrogeochemical data. They reflect the impact of geomedia, hydrogeology, geographic position, and agricultural wastewater. The groundwater is undersaturated with respect to most selected minerals. The groundwater was supersaturated with respect to iron minerals in northern and southern Darb El-Arbaein. The partial pressure of the groundwater versus saturation index of calcite shows the gradual change in PCO₂ from atmospheric to the present aquifer pressures.     

Hydrogeochemical characterization and groundwater quality assessment in the intensive agricultural zone of the Upper Cheliff plain,Algeria

The alluvial aquifer of Upper Cheliff (northern Algeria) is known for its intensive agricultural activities, which is based especially on groundwater exploitation. This aquifer is now facing a dual problem of quantity and quality, with a decrease in the groundwater levels and an increase in mineralization. Twenty monitoring samples were collected and analyzed for major ion during the dry season 2014. In the present study, we try to characterize the hydrogeochemical processes and to assess the impact of natural and anthropogenic conditions on groundwater mineralization. The analytical results of the dry season 2014 show a groundwater quality slightly alkaline (pH > 7) and indicate that the majority of samples have a values exceeding the limits of potability fixed by WHO in 2008, due to the various sources of anthropogenic pollution. The Piper diagram shows the dominance of groundwater types: Ca–Cl, the mixed facies (Cl–SO₄–Ca–Mg), and Ca–HCO₃: The mineralization process in this aquifer is mainly controlled by the lithology of the aquifer (exchange water–rock and weathering of calcareous crust dissolution in the unsaturated zone), by anthropogenic factors (discharges of untreated urban sewage, intensive use of fertilizers in agriculture and the use of domestic septic tanks by rural inhabitants) and also by geoclimatic conditions (semiarid climate). Suitability of groundwater shows more than 80% of samples have very poor quality for drinking and more than 20% of samples indicate a quality unsuitable for irrigation.     

Hydrogeochemical parameters for assessment of groundwater quality in the upper Gunjanaeru River basin,Cuddapah District,Andhra Pradesh,South India

In the management of water resources, quality of water is just as important as its quantity. In order to know the quality and/or suitability of groundwater for domestic and irrigation in upper Gunjanaeru River basin, 51 water samples in post-monsoon and 46 in pre-monsoon seasons were collected and analyzed for various parameters. Geological units are alluvium, shale and quartzite. Based on the analytical results, chemical indices like percent sodium, sodium adsorption ratio, residual sodium carbonate, permeability index (PI) and chloroalkaline indices were calculated. The pre-monsoon waters have low sodium hazard as compared to post-monsoon season. Residual sodium carbonate values revealed that one sample is not suitable in both the seasons for irrigation purposes due the occurrence of alkaline white patches and low permeability of the soil. PI values of both seasons revealed that the ground waters are generally suitable for irrigation. The positive values of Chloroalkaline indices in post-monsoon (80%) and in pre-monsoon (59%) water samples indicate absence of base-exchange reaction (chloroalkaline disequilibrium), and remaining samples of negative values of the ratios indicate base-exchange reaction (chloroalkaline equilibrium). Chadha rectangular diagram for geochemical classification and hydrochemical processes of groundwater for both seasons indicates that most of waters are Ca–Mg–HCO₃ type. Assessment of water samples from various methods indicated that majority of the water samples in both seasons are suitable for different purposes except at Yanadipalle (sample no. 8) that requires precautionary measures. The overall quality of groundwater in post-monsoon season in all chemical constituents is on the higher side due to dissolution of surface pollutants during the infiltration and percolation of rainwater and at few places due to agricultural and domestic activities.     

Source of salinity in the groundwater of Lenjanat Plain,Isfahan, Iran

The present study aimed at identifying the salinity source in the groundwater of Lenjanat Plain. To do so, non-isotopic geochemical methods were employed: groundwater samples were collected seasonally from 33 wells widespread in the area, and physicochemical parameters as well as major and minor elements were measured in the 132 samples. The data collected from the field and laboratory measurements were interpreted through statistical and hydrogeochemical graphs, mass ratios and saturation indexes obtained from modeling. The results revealed that hydrogeochemical properties of the study aquifer were controlled by rock/water interactions including ion exchange, dissolution of evaporation deposits (halite and gypsum) and precipitation/dissolution of carbonates. Based on the values of Cl/Br ratio in Lenjanat groundwater (329–4,492), dissolution of evaporation deposits in aquifer was the main cause for groundwater salinity. Considering the Lenjanat groundwater geochemical properties, the data confirm the reported Cl/Br ratios for groundwater affected by the dissolution of evaporation deposits (Cl/Br > 300) and overlaps with the range of Cl/Br ratios for domestic sewage effluent groundwater. Selecting the best chemical components and their ratios in non-isotopic geochemical methods provides an accurate distinction between sources of groundwater salinity.     

Hydrochemical analysis and evaluation of groundwater quality of a Mio-Plio-Quaternary aquifer system in an arid regions: case of El Hancha, Djebeniana and El Amra regions, Tunisia

A hydrogeochemical approach has been carried out in the Mio-Plio-Quaternary aquifer system of northern Sfax to investigate the geochemical evolution, the origin of groundwaters and their circulation patterns. The groundwater samples collected from different wells seem to be dominated by sodium chloride type to sulphate chloride type. Detail analysis of chemical data including the thermodynamic calculations was used to assess that the chemical evolution of groundwater is primarily controlled by water–rock interactions. The values of sodium absorption ratio and electrical conductivity of the groundwater were plotted in the US Salinity Laboratory diagram for irrigation water. Most of the water samples in northern Sfax fall in the fields of C4S1, C4S2 and C4S3 indicating very high salinity and medium to high sodium alkalinity hazard. Thus, groundwater quality is ranging between doubtful to unsuitable for irrigation uses under normal condition, and further action for salinity control is required in remediating such problem. Principal component analysis of geochemical data used in conjunction with bivariate diagrams of major elements indicates that groundwater mineralization is mainly controlled by (1) water–rock interaction processes, (2) anthropogenic process in relation with return flow of NO₃-rich irrigation waters and (3) domestic discharges.     

Characteristic of groundwater potentialities in West Nile Valley South,Minia Governorate,Egypt

The main aim of the present study is to detect the status of groundwater resources in west Mallawi area which represented one of the new reclamation lands. In order to achieve this aim, the hydrogeological and hydrogeochemical studies are carried out, based on the results of 21 pumping tests and chemical analysis of 29 water samples. Two water-bearing units are detected in the study area, namely, the Eocene fractured limestone aquifer which occupies the east portion of the studied area. The second aquifer consists of friable sediments of sand and gravel and may be related to the late Oligocene–early Miocene age and overlies the limestone rocks in the west, and this aquifer were studied for the first time in this work. Regionally, the groundwater flow in the area under study occurs toward the north and east directions. There is a hydraulic connection between both aquifers through the structural pattern affected the area. The partial recharge of the both aquifers takes place through the upward leakage from deep aquifers and the Nile water. There is a general decrease in the water salinity from west to east direction. The groundwater of both aquifers was evaluated for the different purposes and concluded that, it is considered suitable for different uses.     

The hydrogeochemical characterization of Morsott-El Aouinet aquifer, Northeastern Algeria

A study of the hydrogeochemical processes in the Morsott-El Aouinet aquifer was carried out with the objective of identifying the geochemical processes and their relation with groundwater quality as well as to get an insight into the hydrochemical evaluation of groundwater. The high salinity coupled with groundwater level decline pose serious problems for current irrigation and domestic water supplies as well as future exploitation. A combined hydrogeologic and isotopic investigation have been carried out using chemical and isotopic data to deduce a hydrochemical evaluation of the aquifer system based on the ionic constituents, water types, hydrochemical facies and factors controlling groundwater quality. The ionic speciation and mineral dissolution/precipitation was calculated by WATEQF package software. The increase in salinity is related to the dissolution and/or precipitation processes during the water–rock interaction and to the cationic exchange reactions between groundwater and clay minerals. The isotopic analysis of some groundwater samples shows a similarity with the meteoric waters reflect their short residence time and a lowest evaporation phenomenon of infiltrated groundwater.     

Hydrogeochemical characteristics of surface water (SW) and groundwater (GW) of the Chinnaeru River basin,northern part of Nalgonda District,Andhra Pradesh,India

Groundwater and surface water samples from 47 locations (28 groundwater, 10 tanks and 9 stream channel) were collected during the pre-monsoon (May–June) and post-monsoon season (November) from Chinnaeru River basin. Chinnaeru River basin is situated 30 km east of Hyderabad City and its area covers 250 km² and falls in the Survey of India Toposheet No. 56 K/15. The extensive agricultural, industrial and urbanization activities resulted in the contamination of the aquifer. To study the contamination of groundwater, water samples were collected from an area and analyzed for major cations and anions. Various widely accepted methods such as salinity, sodium absorption ratio, Kelly’s ratio, residual sodium carbonate, soluble sodium percentage, permeability index and water quality index are used to classify groundwater and surface water (tank and stream) for drinking as well as irrigation purposes. Besides this, Piper trilinear diagram, Wilcox diagram, Doneen’s classification and Gibb’s plot were studied for geochemical controls, and hydrogeochemistry of groundwater and surface water samples were studied.     

Assessment of hydrogeochemistry and contamination of Varamin deep aquifer,Tehran Province,Iran

The present study investigates the hydrogeochemistry and contamination of Varamin deep aquifer located in the southeast of Tehran province, Iran. The study also evaluates groundwater suitability for irrigation uses. The hydrogeochemical study was conducted by collecting and analyzing 154 groundwater samples seasonally during 2014. Based on evolutionary sequence of Chebotarev, the aquifer is in the stage of SO₄ + HCO₃ in the north half of the plain and it has evolved into SO₄ + Cl in the south half. The unusual increase in TDS and Cl^? toward the western boundaries of the aquifer indicates some anomalies. These anomalies have originated from discharge of untreated wastewater of Tehran city in these areas. The studied aquifer contains four dominant groundwater types including Na–Ca–SO₄ (55%), Na–Ca–HCO₃ (22%), Na–Cl (13%) and Ca–Cl (10%). The spatial distributions of Na–Cl and Ca–Cl water types coincide with observed anomalies. Ionic relationships of SO₄ ^2? versus Cl^? and Na⁺ versus Cl^? confirm that water–rock interaction and anthropogenic contribution are main sources of these ions in the groundwater. The main processes governing the chemistry of the groundwater are the dissolution of calcite, dolomite and gypsum along the flow path, and direct ion exchange. Reverse ion exchange controls the groundwater chemistry in the areas contaminated with untreated wastewater. Based on Na% and SAR, 10.3 and 27% of water samples are unsuitable for irrigation purposes, respectively. Regarding residual sodium carbonate, there is no treat for crop yields. Only 6% of water samples represent magnesium adsorption ratios more than 50% which are harmful and unsuitable for irrigation.     

Study of hydrogeochemical processes of the groundwater in Ghatprabha river sub-basin, Bagalkot District, Karnataka, India

The alluvial aquifer of the Ghatprabha River comprises shallow tertiary sediment deposits underlain by peninsular gneissic complex of Archean age, located in the central–eastern part of the Karnataka in southern India. In order to establish the baseline hydrochemical conditions and processes determining the groundwater quality, groundwater samples were collected as part of an integrated investigation that coupled multivariate statistical analysis with hydrochemical methods to identify and interpret the groundwater chemistry of the aquifer system. Three main hydrochemical types (Ca–Mg–Cl, Ca–Mg–HCO₃, and Na–SO₄) were identified. Gibbs plots indicate that the evolution of water chemistry is influenced by water–rock interaction followed by evapotranspiration process. The results of factor analysis indicated the total variance explained by the extracted factor 79.9% and 87.1% for both pre- and post-monsoon, respectively. And other processes such as silicate weathering, ion exchange, and local anthropogenic activities affect the groundwater chemistry.     

Identification of a Holocene aquifer–lagoon system using hydrogeochemical data

The hydrogeochemical characteristics of the Cabo de Gata coastal aquifer (southeastern Spain) were studied in an attempt to explain the anomalous salinity of its groundwater. This detritic aquifer is characterised by the presence of waters with highly contrasting salinities; in some cases the salinity exceeds that of seawater. Multivariate analysis of water samples indicates two groups of water (G1 and G2). Group G1 is represented in the upper part of the aquifer, where the proportion of seawater varies between 10 and 60%, whilst G2 waters, taken from the lower part of the aquifer, contain 60−70% seawater. In addition, hydrogeochemical modelling was applied, which reveals that the waters have been subject to evaporation between 25 and 35%. There was a good agreement between the modelled results and the observed water chemistry. This evaporation would have occurred during the Holocene, in a coastal lagoon environment; the resulting brines would have infiltrated into the aquifer and, due to their greater density, sunk towards the impermeable base. The characteristics of this water enabled us to reconstruct the interactions that must have occurred between the coastal aquifer and the lagoon, and to identify the environmental conditions that prevailed in the study area during the Middle Holocene.     

Investigation of the hydrogeochemical processes in an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa

An investigation was conducted to assess the hydrogeochemical processes of an alluvial channel aquifer located in a typical Karoo Basin of Southern Africa. The investigation was aimed at identifying and describing the groundwater chemistry evolution and its contribution to the overall groundwater quality. X-ray fluorescent spectrometry (XRF) and X-ray diffractometry (XRD) analyses were performed on geological samples to identify and quantify the major element oxides and minerals. The study utilises the conventional Piper diagram, bivariate plots and PHREEQC hydrogeochemical model to analyse groundwater chemistry data obtained during the wet (February and May) and dry seasons (August and December) of 2011. The XRF and XRD results show that the channel deposits are dominated by SiO₂ element oxides and quartz minerals, thus elevated concentrations of silicon (Si⁴⁺) were found in the groundwater. Dolomite and calcite minerals were also detected in the unconsolidated aquifer sediments. The detailed study of the alluvial aquifer system has shown that dissolution of dolomite and calcite minerals and ion exchange are the dominant hydrogeochemical processes influencing the groundwater quality. The groundwater evolves from Ca²⁺–Mg²⁺–HCO₃ ^? recharge water that goes through ion exchange with Na⁺ in the clay-silt sediment to give a Na⁺–HCO₃ ^? water type. The groundwater is supersaturated with respect to quartz, dolomite and calcite minerals. The study shows the potential usefulness of simple bivariate plots as a complimentary tool to the conventional methods for analyzing groundwater hydrogeochemical processes.     

Hydrogeochemistry and arsenic contamination of groundwater in the Rayen area, southeastern Iran

High As contents in groundwater were found in Rayen area and chosen for a detailed hydrogeochemical study. A total of 121 groundwater samples were collected from existing tube wells in the study areas in January 2012 and analyzed. Hydrogeochemical data of samples suggested that the groundwater is mostly Na–Cl type; also nearly 25.62 % of samples have arsenic concentrations above WHO permissible value (10 μg/l) for drinking waters with maximum concentration of aqueous arsenic up to 25,000 μg/l. The reducing conditions prevailing in the area and high arsenic concentration correlated with high bicarbonate and pH. Results show that arsenic is released into groundwater by two major phenomena: (1) through reduction of arsenic-bearing iron oxides/oxyhydroxides and Fe may be precipitated as iron sulfide when anoxic conditions prevail in the aquifer sediments and (2) transferring of As into the water system during water–acidic volcanic rock interactions.