A pragmatic approach to study the groundwater quality suitability for domestic and agricultural usage,Saq aquifer,northwest of Saudi Arabia

The present study deals with detailed hydrochemical assessment of groundwater within the Saq aquifer. The Saq aquifer which extends through the NW part of Saudi Arabia is one of the major sources of groundwater supply. Groundwater samples were collected from about 295 groundwater wells and analyzed for various physico-chemical parameters such as electrical conductivity (EC), pH, temperature, total dissolved solids (TDS), Na⁺, K⁺, Ca²⁺, Mg²⁺, CO₃ ^?, HCO₃ ^?, Cl^?, SO₄ ^2?, and NO₃ ^?. Groundwater in the area is slightly alkaline and hard in nature. Electrical conductivity (EC) varies between 284 and 9,902?μS/cm with an average value of 1,599.4 μS/cm. The groundwater is highly mineralized with approximately 30 % of the samples having major ion concentrations above the WHO permissible limits. The NO₃ ^? concentration varies between 0.4 and 318.2 mg/l. The depth distribution of NO₃ ^? concentration shows higher concentration at shallow depths with a gradual decrease at deeper depths. As far as drinking water quality criteria are concerned, study shows that about 33 % of samples are unfit for use. A detailed assessment of groundwater quality in relation to agriculture use reveals that 21 % samples are unsuitable for irrigation. Using Piper’s classification, groundwater was classified into five different groups. Majority of the samples show Mix-Cl-SO₄- and Na-Cl-types water. The abundances of Ca²⁺ and Mg²⁺ over alkalis infer mixed type of groundwater facies and reverse exchange reactions. The groundwater has acquired unique chemical characteristics through prolonged rock-water interactions, percolation of irrigation return water, and reactions at vadose zone.     

Hydrochemical characterization and pollution assessment of groundwater in Jammu Siwaliks,India

Physico-chemical groundwater (GW) parameters were evaluated to understand the hydrogeochemical processes in the Siwalik plains of Jammu and Kashmir, India. During the 2012–2013 post-monsoon (POM) and pre-monsoon (PRM) seasons, GW samples (n = 207) from deep bore wells and shallow open wells were chemically analysed. Cations (Ca²⁺, Mg²⁺, Na⁺, K⁺ and Fe²⁺) and anions (HCO₃ ^?, Cl^?, SO₄ ^2? and F^?) showed a wide spatio-temporal variation. Results suggest that weathering and dissolution of carbonates and silicate rocks is the main source of water mineralization. The major hydrochemical facies is characterized by Ca-Mg-HCO₃ and Ca-HCO₃ during the PRM and POM seasons respectively. The presence of sulphate-bearing water in a large number of the samples indicates a significant role of gypsum dissolution and anthropogenic contamination of the GW. Factor analysis (FA) and hierarchical cluster analysis (HCA) revealed that the variability of hydrochemistry is mainly related to rock-water interaction, dissolution of carbonates and other lithological units as well as the influence of anthropogenic activities in the area. Overall, it was found that the GW quality is within the limits of human consumption. The higher concentration of a few chemicals indicates an increasing trend of industrial contamination of the GW. For sustainable development of the portable GW in Siwaliks, it is necessary to minimize the adverse impacts of the anthropogenic and industrial contamination on the GW resources through best management practices and prevent its further contamination to a level that could make GW unsuitable for human uses.     

Delineating shallow saline groundwater zones from Southern India using geophysical indicators

A geophysical survey was conducted over an industrial belt encompassing 80 functional leather factories in Southern India. These factories discharge untreated effluents which pollute shallow groundwater where electrical conductivity (EC) value had a wide range between 545 and 26,600 μS/cm (mean, 3, 901 μS/cm). The ranges of Na⁺ and Cl^? ions were from 46 to 4,850 mg/L (mean, 348 mg/L) and 25 to 10,390 mg/L (mean, 1,079 mg/L), respectively. Geoelectrical layer parameters of 37 vertical electrical soundings were analyzed to demarcate fresh and saline water zones. However, the analysis not did lead to a unique resolution of saline and fresh waters. It was difficult to assign a definitive value to the aquifer resistivity of any area. Thus, geophysical indicators, namely longitudinal unit conductance (S), transverse unit resistance (T), and average longitudinal resistivity (R _s), were calculated for identifying fresh and saline waters. Spatial distributions of S, T, and R _s reflected widely varying ranges for the saline and fresh water zones. Further, the empirical relation of formation factor (F) was established from pore-water resistivity and aquifer resistivity for fresh and saline aquifers, which may be used to estimate local EC values from the aquifer resistivity, where well water is not available.     

Assessment of geochemical processes occurring in groundwaters in the coastal alluvial aquifer

Groundwater samples are collected from 30 observation wells in the study area to analyze the hydrochemical quality for determining the seawater encroachment in the part of Central Godavari Delta, Bay of Bengal, India. In order to establish the baseline hydrochemical conditions and processes determining the groundwater quality, an integrated investigation coupled with multivariate statistical analysis and hydrochemical methods are used to identify and interpret the groundwater chemistry of the aquifer system. The major land use is irrigated agriculture and aquaculture in the study area. The ground waters affected by the seawater intrusion featured high levels of sodium (Na⁺), chloride (Ca⁺), and TDS, which are the simplest common indicators for seawater influence. The elevated levels of NO₃–N at some monitoring wells indicate nitrate pollution of groundwater due to anthropogenic origin such as septic effluents or chemical fertilizers. Besides the major chemical compositions, it was also demonstrated that ionic ratios would be useful to delineate seawater intrusion and they include Na⁺/Ca²⁺, Mg²⁺/Ca²⁺, SO₄ ^2?/Ca²⁺, Na⁺/(Na⁺?+?Cl^?), and Ca^?/sum of anions. This paper demonstrates the variations in hydrochemical quality of groundwater and its evolution processes in two different seasons in the coastal aquifer alluvial settings     

Hydrogeochemical characterization of contaminated groundwater in Patancheru industrial area,southern India

The groundwater is one of the most contaminated natural resources in Patancheru industrial area due to unplanned and haphazard industrial growth and urbanization without following basic pollution control norms. The rapid industrialization initiated in early 1970 has started showing up its after effects few years later in the form of physiochemical contamination of the both surface and groundwater bodies of the area. It has resulted in local people being deprived of safe drinking water, plant and aquatic life has severely affected, and situation is deteriorating over the years in the area in spite of some preventive and remedial measures being initiated. The focus of the present study is to understand the chemical characteristics of groundwater and geochemical processes the contaminant water is undergoing which are normally imprinted in its ionic assemblages. The water samples collected in pre- and post-monsoon seasons from forty two groundwater and four surface water sources were analyzed for major constituents such as Ca²⁺, Mg²⁺, Na⁺, K⁺, CO₃⁻, HCO₃⁻, Cl⁻, SO₄²⁻, NO₃⁻, and F⁻, and selected samples were tested for ten important trace metals like Fe, Pb, Bi, Mn, Cr, Co, Ni, Cu, Zn, and Cd. Na⁺ among cations and Cl⁻ among anions dominate the water in both the seasons where as Ca²⁺, HCO₃⁻, and Cl⁻ show significant reduction in their ionic strength in post-monsoon. The groundwater in general is of mixed type, but most of it belong to Na⁺–Cl⁻, Na⁺–HCO₃⁻, Ca²⁺–Mg²⁺–HCO₃⁻, and Ca²⁺–Mg²⁺–Cl⁻ facies. The Na⁺ and Ca²⁺ are in the transitional state with Na⁺ replacing Ca²⁺ and HCO₃⁻–Cl⁻ due to physiochemical changes in the aquifer system. The evaluation of hydrochemistry through various ionic indices, ratios, and plots suggest that silicate–carbonate weathering, ion exchange, dissolution, and evaporation processes are responsible for origin of the present chemical status of the groundwater which is also controlled by the contamination from extraneous sources that could have accelerated the dissolution processes. Gibbs plots authenticate that the evolution of water chemistry is influenced by interaction of percolating water with aquifer matrix apart from anthropogenic enrichment of elements which get over concentrated due to evaporation.     

Leachate Characterization and Assessment of Groundwater Pollution Near Municipal Solid Waste Landfill Site

Leachate and groundwater samples were collected from Gazipur landfill-site and its adjacent area to study the possible impact of leachate percolation on groundwater quality. Concentration of various physico-chemical parameters including heavy metal (Cd, Cr, Cu, Fe, Ni, Pb and Zn) and microbiological parameters (total coliform (TC) and faecal coliform (FC)) were determined in groundwater and leachate samples. The moderately high concentrations of Cl⁻, NO⁻ ₃, SO²⁻ ₄, NH⁺ ₄, Phenol, Fe, Zn and COD in groundwater, likely indicate that groundwater quality is being significantly affected by leachate percolation. Further they proved to be as tracers for groundwater contamination. The effect of depth and distance of the well from the pollution source was also investigated. The presence of TC and FC in groundwater warns for the groundwater quality and thus renders the associated aquifer unreliable for domestic water supply and other uses. Although some remedial measures are suggested to reduce further groundwater contamination via leachate percolation, the present study demand for the proper management of waste in Delhi.     

Arsenic-safe alternate aquifers and their hydraulic characteristics in contaminated areas of Middle Ganga Plain, Eastern India

Arsenic groundwater contamination exceeding 0.05 mg/l affecting the Newer Alluvial tracts of Patna and Bhojpur, the two worst affected districts located in the Middle Ganga Plain in the Bihar state, has been studied The area is underlain by two-tier Quaternary aquifer systems within a depth of 300 m below ground level, separated by a 15?C32-m-thick clay/sandy clay aquitard. The upper part (<50 m depth) of the shallow aquifer system is arsenic-contaminated. The deeper aquifer system (lying below 120?C130 m depth) exhibits low arsenic load (max 0.0035 mg/l), having hydraulic conductivity between 64.88 and 82.04 m/day. Groundwater in the deeper aquifer occurs under semi-confined to confined condition due to poor hydraulic conductivity of the middle clay (4.7 × 10^???2???7.2 × 10^???3 m/day). Hydraulic head of the deeper aquifer remains close to the surface than the shallow aquifer. The two aquifer systems in the Newer Alluvium are replaced by a thick single aquifer system in the adjoining Older Alluvium, within a depth of 330 m below ground. In the arsenic-contaminated area, deeper aquifer is protected by a middle clay, which may be developed for community drinking water supply by deep tube wells having a yield capacity of 150 m³/h.     

Modelling of lindane transport in groundwater of metropolitan city Vadodara,Gujarat, India

Migration pattern of organochloro pesticide lindane has been studied in groundwater of metropolitan city Vadodara. Groundwater flow was simulated using the groundwater flow model constructed up to a depth of 60 m considering a three-layer structure with grid size of 40?×?40?×?40 m³. The general groundwater flow direction is from northeast to south and southwest. The river Vishwamitri and river Jambua form natural hydrologic boundary. The constant head in the north and south end of the study area is taken as another boundary condition in the model. The hydraulic head distribution in the multilayer aquifer has been computed from the visual MODFLOW groundwater flow model. TDS has been computed though MT3D mass transport model starting with a background concentration of 500 mg/l and using a porosity value of 0.3. Simulated TDS values from the model matches well with the observed data. Model MT3D was run for lindane pesticide with a background concentration of 0.5?μg/l. The predictions of the mass transport model for next 50 years indicate that advancement of containment of plume size in the aquifer system both spatially and depth wise as a result of increasing level of pesticide in river Vishwamitri. The restoration of the aquifer system may take a very long time as seen from slow improvement in the groundwater quality from the predicted scenarios, thereby, indicating alarming situation of groundwater quality deterioration in different layers. It is recommended that all the industries operating in the region should install efficient effluent treatment plants to abate the pollution problem.     

Physicochemical quality evaluation of groundwater and development of drinking water quality index for Araniar River Basin, Tamil Nadu, India

Groundwater is the most important natural resource which cannot be optimally used and sustained unless its quality is properly assessed. In the present study, the spatial and temporal variations in physicochemical quality parameters of groundwater of Araniar River Basin, India were analyzed to determine its suitability for drinking purpose through development of drinking water quality index (DWQI) maps of the post- and pre-monsoon periods. The suitability for drinking purpose was evaluated by comparing the physicochemical parameters of groundwater in the study area with drinking water standards prescribed by the World Health Organization (WHO) and Bureau of Indian Standards (BIS). Interpretation of physicochemical data revealed that groundwater in the basin was slightly alkaline. The cations such as sodium (Na⁺) and potassium (K⁺) and anions such as bicarbonate (HCO₃ ^?) and chloride (Cl^?) exceeded the permissible limits of drinking water standards (WHO and BIS) in certain pockets in the northeastern part of the basin during the pre-monsoon period. The higher total dissolved solids (TDS) concentration was observed in the northeastern part of the basin, and the parameters such as calcium (Ca²⁺), magnesium (Mg²⁺), sulfate (SO₄ ^2?), nitrate (NO₃ ^?), and fluoride (F^?) were within the limits in both the seasons. The hydrogeochemical evaluation of groundwater of the basin demonstrated with the Piper trilinear diagram indicated that the groundwater samples of the area were of Ca²⁺-Mg²⁺-Cl^?-SO₄ ^2?, Ca²⁺-Mg²⁺-HCO₃ ^? and Na⁺-K⁺-Cl^?-SO₄ ^2? types during the post-monsoon period and Ca²⁺-Mg²⁺-Cl^?-SO₄ ^2?, Na⁺-K⁺-Cl^?-SO₄ ^2? and Ca²⁺-Mg²⁺-HCO₃ ^? types during the pre-monsoon period. The DWQI maps for the basin revealed that 90.24 and 73.46 % of the basin area possess good quality drinking water during the post- and pre-monsoon seasons, respectively.     

Major ion chemistry of shallow groundwater of a fast growing city of Central India

Nagpur City located in semiarid area of central India is a fast-growing industrial centre. In recent years, rapid development has created an increased demand for drinking water, which is increasingly being fulfilled by groundwater abstraction. The present study was undertaken to assess major ion chemistry of shallow groundwater to understand geochemical evolution of groundwater and water quality for promoting sustainable development and effective management of groundwater resources. A total of 47 water samples were collected from shallow aquifer of selected parts of the city and the water chemistry of various ions viz. Ca^2 +, Mg^2 +, Na⁺, K⁺, CO₃  ^2-_{3}^{\ \, 2-}, HCO₃  ^-_{3}^{\ \, -}, Cl⁻, SO₄  ^2-_{4}^{\ \,2-} and NO₃  ^-_{3}^{\ \,-} are carried out. The chemical relationships in Piper diagram identify Ca–HCO₃–Cl and mixed Ca–Na–HCO₃–Cl as most prevalent water types. Alkaline earth exceeds alkalis and weak acids exceed strong acids. Ionic ratios and Gibb’s diagram suggest that silicate rock weathering and anthropogenic activities are the main processes that determine the ionic composition in the study area. The nitrate appeared as a major problem of safe drinking water in this region. We recorded highest nitrate concentration, i.e., 411 mg/l in one of the dug well. A comparison of groundwater quality in relation to drinking water quality standards revealed that about half of the shallow aquifer samples are not suitable for drinking.     

The occurrence and hydrochemistry of fluoride and boron in carbonate aquifer system, central and western Estonia

Silurian–Ordovician (S–O) aquifer system is an important drinking water source of central and western Estonia. The fluoride and boron contents of groundwater in aquifer system vary considerably. The fluoride concentration in 60 collected groundwater samples ranged from 0.1 to 6.1 mg/l with a mean of 1.95 mg/l in the study area. Boron content in groundwater varied from 0.05 mg/l to 2.1 mg/l with a mean value of 0.66 mg/l. Considering the requirements of EU Directive 98/83/EC and the Estonian requirements for drinking water quality, the limit value for fluoride (1.5 mg/l) and for boron (1.0 mg/l) is exceeded in 47 and 28 % of wells, respectively. Groundwater with high fluoride and boron concentrations is found mainly in western Estonia and deeper portion of aquifer system, where groundwater chemical type is HCO₃–Cl–Na–Mg–Ca, water is alkaline, and its Ca²⁺ content is low. Groundwater of the study area is undersaturated with respect to fluorite and near to equilibrium phase with respect to calcite. The comparison of TDS versus Na/(Na?+?Ca) and Cl/(Cl?+?HCO₃) points to the dominance of rock weathering as the main process, which promotes the availability of fluoride and boron in the groundwater. The geological sources of B in S–O aquifer system have not been studied so far, but the dissolution of fluorides from carbonate rocks (F?=?100–400 mg/kg) and K-bentonites (F?=?2,800–4,500 mg/kg) contributes to the formation of F-rich groundwater.     

Groundwater quality and its suitability for drinking and agricultural use in the Yanqi Basin of Xinjiang Province, Northwest China

The Yanqi Basin in Xinjiang Province is an important agricultural area with a high population density. The extensive agricultural activities in the Yanqi Basin started in the 1950s with flood irrigation techniques. Since then, the groundwater table was raised because of the absence of an efficient drainage system. This obstacle is a crucial factor that restricts sustainable socioeconomic development. Hydrochemical investigations were conducted in the Yanqi Basin, Northwestern China, to determine the chemical composition of groundwater. Sixty groundwater samples were collected from different wells to monitor the water chemistry of various ions. The results of the chemical analysis indicate that the groundwater in the area is generally neutral to slightly alkaline and predominantly contains Na⁺ and Ca²⁺ cations as well as HCO₃ ^? and SO₄ ²⁺ anions. High positive correlations between HCO₃ ^?–Mg²⁺ + Ca²⁺, SO ₄ ^2?–Mg²⁺, SO₄ ^2?–Na⁺ + K⁺, and Cl^?–Na⁺ + K⁺ were obtained. The total dissolved solids (TDS) mainly depend on the concentration of major ions such as HCO₃ ^?, SO₄ ^2?, Cl^?, Ca²⁺, Mg²⁺, and Na⁺ + K⁺. The dominant hydrochemical facies for groundwater are Ca²⁺–Mg²⁺–HCO₃ ^?, Mg²⁺–Ca²⁺–SO₄ ^2?–Cl^?, Na⁺–K⁺–Cl^?–SO₄ ^2?, and Na⁺–K⁺–Mg²⁺–Cl^?–HCO₃ ^? types. The hydrochemical processes are the main factors that determine the water quality of the groundwater system. These processes include silicate mineral weathering, dissolution, ion exchange, and, to a lesser extent, evaporation, which seem to be more pronounced downgradient of the flow system. The saturation index (SI), which is calculated according to the ionic ratio plot, indicates that the gypsum–halite dissolution reactions occur during a certain degree of rock weathering. SI also indicates that evaporation is the dominant factor that determines the major ionic composition in the study area. The assessment results of the water samples using various methods indicate that the groundwater in the study area is generally hard, fresh to brackish, high to very high saline, and low alkaline in nature. The high total hardness and TDS of the groundwater in several places indicate the unsuitability of the groundwater for drinking and irrigation. These areas require particular attention, particularly in the construction of adequate drainage as well as in the introduction of an alternative salt tolerance cropping.     

Arsenic mobilization in the Brahmaputra plains of Assam: groundwater and sedimentary controls

Arsenic (As) mobilization to the groundwater of Brahmaputra floodplains was investigated in Titabor, Jorhat District, located in the North Eastern part of India. The groundwater and the aquifer geochemistry were characterized in the study area. The range of As concentration in the groundwater varies from 10 to 440 μg/l with mean concentration 210 μg/l. The groundwaters are characterized by high dissolved Fe, Mn, and HCO₃ ^? and low concentrations of NO₃ ^? and SO₄ ^2? indicating the reduced conditions prevailing in the groundwater. In order to understand the actual mobilization processes in the area, six core drilling surrounding the two target tube wells (T1 and T2) with high As concentration (three drill-cores surrounds each tube well closely) was done. The sediment was analyzed its chemical, mineralogical, and elemental compositions. A selective sequential extraction suggested that most of the As in the sediment is bound to Fe oxides fractions (32 to 50 %) and the competition for adsorption site by anions (PO₄ ^3?) also accounts to significant fractions of the total arsenic extracted. High variability in the extraction as well as properties of the sediment was observed due to the heterogeneity of the sediment samples with different chemical properties. The SEM and EDX results indicate the presence of Fe, Mn coating along with As for most of the sample, and the presence of As associated minerals were calculated using PHREEQC. The mobilization of As into the groundwater was anticipated to be largely controlled by the reductive dissolution of Fe oxides and partly by the competitive anions viz. PO₄ ^3?.     

Groundwater quality assessment in the urban-west region of Zanzibar Island

This paper highlights the levels of anions (nitrate, nitrite, sulfate, bromide, chloride, and fluoride) and cations (potassium, sodium, magnesium, and calcium) in selected springs and groundwater sources in the urban-west region of Zanzibar Island. The levels of total dissolved solids (TDS) and sodium adsorption ratio (SAR) were also studied. Thirty water samples were collected in December 2012 from various types of water sources, which included closed hand-dug wells (CHDW), open hand-dug wells (OHDW), springwater (SW), public bore wells (PBW), and bore wells owned by private individuals (BWP), and analyzed after filtration and sometimes dilution. The cations were analyzed using inductively coupled plasma-optical emission spectrometry (ICP-OES). The anions were analyzed by chemically suppressed ion chromatography (IC). The ranges of the levels of the investigated parameters were as follows: Na 13.68–3,656 mg L^?1, K 2.66–583 mg L^?1, Mg 0.63–131.10 mg L^?1, Ca 16.79–189.9 mg L^?1, Cl^? 8.61–4,340.97 mg L^?1, F^? 0–1.02 mg L^?1, Br^? 0–10.88 mg L^?1, NO₃ ^? 0.18–342.4 mg L^?1, NO₂ ^? 0–1.39, SO₄ ^2? 4.43–534.02 mg L^?1, TDS 7–6,380 mg L^?1, and SAR 0.63–50. Except fluoride, most of the studied parameters in the water samples had concentrations beyond the permissible limits of the World Health Organization (WHO). The elevated concentrations are a result of seepage of contaminated water from on-site septic tanks, pit latrines, landfill leachates, fertilizer applications, and domestic effluents. These results should alert domestic water stakeholders in Zanzibar to the urgent task of initiating a quick mitigation response to control these alarming water risks.     

Heavy metals in the habitat and throughout the food chain of the Neotropical otter, Lontra longicaudis, in protected Mexican wetlands

Top predators like the Neotropical otter, Lontra longicaudis annectens, are usually considered good bioindicators of habitat quality. In this study, we evaluated heavy metal contamination (Hg_tot, Pb, Cd) in the riverine habitat, prey (crustaceans and fish), and otter feces in two Ramsar wetlands with contrasting upstream contamination discharges: Río Blanco and Río Caño Grande in Veracruz, Mexico, during the dry, the wet, and the nortes seasons. Most comparisons revealed no differences between sites while seasonal differences were repeatedly detected for all of the compartments. Higher concentrations of Pb during the dry season and of Cd during the wet season in otter feces mirrored differences detected in the most seasonally consumed prey. Compared with fecal methylmercury values reported for the European otter (0.25–0.75 mg kg^?1) in unprotected areas, the Hg_tot levels that we measured were lower (0.02–0.17 mg kg^?1). However, Pb (117.87 mg kg^?1) and Cd (9.14 mg kg^?1) concentrations were higher (Pb, 38.15 mg kg^?1 and Cd, 4.72 mg kg^?1) in the two Ramsar wetlands. Protected areas may shelter species, but those with water-linked diets may suffer the effect of chemicals used upstream.     

Groundwater quality assessment in semi-arid regions using integrated approaches: the case of Grombalia aquifer (NE Tunisia)

As many arid and semi-arid regions in the Mediterranean Basin, the Grombalia coastal aquifer (NE Tunisia) is affected by severe groundwater exploitation and contamination. Therefore, quality assessments are becoming increasingly important as the long-term protection of water resources is at stake. Multidisciplinary investigations, like the one presented in this paper, are particularly effective in identifying the different origins of mineralization within an aquifer and investigating the impact of anthropogenic activities on groundwater quality. An integrated assessment, focused on the combined use of geostatistical, geochemical and isotopic (δ¹⁸O, δ²H and ³H) tools, was performed in the Grombalia aquifer between February and March 2014. The overall goal was to study the main processes controlling aquifer salinization, with special focus to nitrate contamination. Results indicate a persisting deterioration of water quality over the whole basin except the south-eastern zone juxtaposing the recharge area of the aquifer. Nitrate contents exceed the drinking water standard (50 mg/l) in 70% of groundwater samples, mainly due to the excessive use of fertilizers and urban activities. Stable isotope measurements showed the contribution of modern rainwater to aquifer recharge and proved the presence of evaporation contributing to the salinity increase. Tritium values of groundwater samples suggested two hypotheses: the existence of mixture between old and recent water or/and the existence of two recharge periods of the aquifer, pre- and post-nuclear weapons test. Principal component analysis confirmed the geochemical interpretation, highlighting that water-rock interaction evaporation effect and intensive anthropogenic activities constitute the main processes controlling the regional groundwater mineralization.     

Hydrogeochemistry and Groundwater Quality Assessment of Lower Part of the Ponnaiyar River Basin, Cuddalore District, South India

The Lower Ponnaiyar River Basin forms an important groundwater province in South India constituted by Tertiary formations dominated by sandstones and overlain by alluvium. The region enjoyed artesian conditions 50 years back but at present frequent failure of monsoon and over exploitation is threatening the aquifer. Further, extensive agricultural and industrial activities and urbanization has resulted in the increase in demand and contamination of the aquifer. To identify the sources and quality of groundwater, water samples from 47 bore wells were collected in an area of 154 km² and were analysed for major ions and trace metals. The results reveal that the groundwater in many places is contaminated by higher concentrations of NO₃, Cl, PO₄ and Fe. Four major hydrochemical facies Ca–Mg–Cl, Na–Cl, Ca–HCO₃ and Na–HCO₃ were identified using Piper trilinear diagram. Salinity, sodium adsorption ratio, and sodium percentage indicate that most of the groundwater samples are not suitable for irrigation as well as for domestic purposes and far from drinking water standards. The most serious pollution threat to groundwater is from nitrate ions, which are associated with sewage and fertilizers application. The present state of the quality of the lower part of Ponnaiyar River Basin is of great concern and the higher concentration of toxic metals (Fe and Ni) may entail various health hazards.     

Assessment of phenol infiltration resilience in soil media by HYDRUS-1D transport model for a waste discharge site

The movement of contaminants through soil imparts a variety of geo-environmental problem inclusive of lithospheric pollution. Near-surface aquifers are often vulnerable to contamination from surface source if overlying soil possesses poor resilience or contaminant attenuation capacity. The prediction of contaminant transport through soil is urged to protect groundwater from sources of pollutants. Using field simulation through column experiments and mathematical modeling like HYDRUS-1D, assessment of soil resilience and movement of contaminants through the subsurface to reach aquifers can be predicted. An outfall site of effluents of a coke oven plant comprising of alarming concentration of phenol (4–12.2 mg/L) have been considered for studying groundwater condition and quality, in situ soil characterization, and effluent characterization. Hydrogeological feature suggests the presence of near-surface aquifers at the effluent discharge site. Analysis of groundwater of nearby locality reveals the phenol concentration (0.11–0.75 mg/L) exceeded the prescribed limit of WHO specification (0.002 mg/L). The in situ soil, used in column experiment, possess higher saturated hydraulic conductivity (K _S ?=?5.25?×?10^?4 cm/s). The soil containing 47 % silt, 11 % clay, and 1.54 % organic carbon content was found to be a poor absorber of phenol (24 mg/kg). The linear phenol adsorption isotherm model showed the best fit (R ²?=?0.977, RMSE?=?1.057) to the test results. Column experiments revealed that the phenol removal percent and the length of the mass transfer zone increased with increasing bed heights. The overall phenol adsorption efficiency was found to be 42–49 %. Breakthrough curves (BTCs) predicted by HYDRUS-1D model appears to be close fitting with the BTCs derived from the column experiments. The phenol BTC predicted by the HYDRUS-1D model for 1.2 m depth subsurface soil, i.e., up to the depth of groundwater in the study area, showed that the exhaustion point was reached within 12 days of elapsed time. This clearly demonstrated poor attenuation capacity of the soil to retard migration of phenol to the groundwater from the surface outfall site. Suitable liner, based on these data, may be designed to inhibit subsurface transport of phenol and thereby to protect precious groundwater from contamination.     

GC estimation of organic hydrocarbons that threaten shallow Quaternary sandy aquifer Northwestern Gulf of Suez,Egypt

Soil and groundwater contamination is one of the important environmental problems at petroleum-related sites, which causes critical environmental and health defects. Severe petroleum hydrocarbon contamination from coastal refinery plant was detected in a shallow Quaternary sandy aquifer is bordered by Gulf in the Northwestern Gulf of Suez, Egypt. The overall objective of this investigation is to estimate the organic hydrocarbons in shallow sandy aquifers, released from continuous major point-source of pollution over a long period of time (91 years ago). This oil refinery contamination resulted mainly in the improper disposal of hydrocarbons and produced water releases caused by equipment failures, vandalism, and accidents that caused direct groundwater pollution or discharge into the gulf. In order to determine the fate of hydrocarbons, detailed field investigations were made to provide intensive deep profile information. Eight composite randomly sediment samples from a test plot were selected for demonstration. The tested plot was 50 m long?×?50 m wide?×?70 cm deep. Sediment samples were collected using an American auger around the point 29° 57′ 33″ N and 32° 30′ 40″ E in 2012 and covered an area of 2,500 m² which represents nearly 1/15 of total plant area (the total area of the plant is approximately 3.250 km²). The detected total petroleum hydrocarbons (TPHs) were 2.44, 2.62, 4.54, 4.78, 2.83, 3.22, 2.56, and 3.13 wt%, respectively. TPH was calculated by differences in weight and subjected to gas chromatography (GC). Hydrocarbons were analyzed on Hewlett–Packard (HP-7890 plus) gas chromatograph equipped with a flame ionization detector (FID). The percentage of paraffine of the investigated TPH samples was 7.33, 7.24, 7.58, 8.25, 10.25, 9.89, 14.77, and 17.53 wt%, respectively.