Open access peer-reviewed chapter

Hydrogeology and Groundwater Geochemistry of the Clastic Aquifer and Its Assessment for Irrigation, Southwest Kuwait

Written By

Fawzia Mohammad Al-Ruwaih

Submitted: 15 May 2017 Reviewed: 10 October 2017 Published: 20 December 2017

DOI: 10.5772/intechopen.71577

From the Edited Volume

Aquifers - Matrix and Fluids

Edited by Muhammad Salik Javaid and Shaukat Ali Khan

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Abstract

Al-Atraf field, is located southwest of Kuwait City, the groundwater is produced from the Kuwait Group aquifer. The objectives are to identify aquifer type and its characteristics. The major geochemical processes operating in the aquifer have to be revealed. In addition, to evaluate the groundwater quality and its suitability of drinking and agriculture usage, an investigation was carried out by estimating physiochemical parameters like pH, EC, TDS, TH, Na+, K+ Ca2+, Mg2+, Cl−, HCO3−, SO42−, total alkalinity, and SiO2. Irrigation parameters like SAR, %Na, RSC, potential salinity, magnesium ratio, Kelly?s ratio, permeability index, and chloro-alkaline index have been determined. The aquifer is confined and occupied by brackish groundwater mainly of NaCl type. Gibb?s plot suggests that the chemical weathering of rock primarily controls the chemistry of the study area. WATEVAL program revealed that the main geochemical processes are silicate weathering, dissolution, precipitation, and reverse ion exchange. WATEQ4F indicates that the groundwater is oversaturated with respect to calcite and dolomite and undersaturated with respect to gypsum and anhydrite. The high total hardness and TDS identify the unsuitability of groundwater for drinking, while irrigation parameters indicate that this water cannot be used on soil without special management for salinity control and salt tolerance plants.

Keywords

  • Kuwait Group aquifer
  • saturation index
  • geochemical processes
  • Gibb’s ratio
  • irrigation parameters

1. Introduction

The State of Kuwait is located at the northwestern side of the Arabian Gulf and occupies an area of about 18,000 km2. Kuwait is bordered on the north and west by Iraq and on the south by the Kingdom of Saudi Arabia. The climate is extremely hot and dry in summer and mild-to-cold in winter. The rainfall is scarce and limited to the period from October to May. The highest ever temperature recorded in Kuwait was 54°C on July 2016. The average annual precipitation recorded during the period 2001–2016 is 114.5 mm. It lies within an arid-semiarid zone lacking renewable surface water. The natural water resources are the brackish groundwater located in the Kuwait Group and the Dammam Formation aquifers, which have been utilized since 1953 on a small scale and for limited purpose, but with increasing population and growth of demands, the production of groundwater embarked on a wide scale project to provide consumers with it through a separate pipe network. This groundwater is used for blending with distilled water for fresh water production, irrigation and landscaping plus household purposes, livestock watering, and construction works. The present total output installed capacity of groundwater wells is around 145 MIGD, meanwhile the maximum consumption hit 114.6 MIGD. However, the demand for water in Kuwait is met from three sectors: desalination, brackish groundwater, and tertiary treated waste water.

The Al-Atraf field is one of the brackish groundwater fields and is located southwest of Kuwait between 29° 18 to 29° 24 north latitudes and 47° 31 to 47° 38 east longitudes. The area under study is about 87.75 km2 and includes 83 water wells, producing groundwater from the Kuwait Group aquifer, where the nominal production capacity is 30 MIGPD. The salinity of the aquifer ranges from 3504 to 6366 mg/l, with an average value of 4441 mg/l.

1.1. Topography

The topography of Kuwait is generally flat, with a gentle rise from sea level at the coast to an elevation of about 270 m in the southwest corner of the country (Figure 1). Local relief is low except in the Jal-Az-Zor escarpment, the Ahmadi Ridge, the Wara Hill, and the Wadi Al-Batin [1]. The Jal-Az-Zor escarpment, about 60 km in length and 145 m in height above MSL, borders the northwestern shore of Kuwait Bay. It trends from Al-Atraf southwest to Bahra northeast. The Ahmadi Ridge parallels to the coastline south of Kuwait City and rises to a height of 137 m above MSL. The east and west slopes of the ridge are very gentle. Another elevation is the Wara Hill, located southeastern Kuwait and has a local relief of about 31 m. The Wadi Al-Batin is a major and shallow depression marking the western boundary of the country for a distance of 75 km with an average width of 6–8 km. The central part of Kuwait and the Neutral Zone are featureless with few wadis and little vegetation. Furthermore, small and shallow depressions exist throughout the northern, western, and central areas. The northern and the western parts of the country have a dense drainage pattern of small and shallow wadi systems, draining northeast toward the Iraq border and toward the shallow depressions near Al-Rawdhatain [2].

Figure 1.

The topographic and the dominant northeast drainage patterns of Kuwait.

1.2. General stratigraphy

The surface of Kuwait is formed by sedimentary rocks and sediments ranging from Middle Eocene to Recent. The Dammam Formation represents the oldest exposed sedimentary rocks. The Recent deposits of fine-grained beach sands cover the southern coast of Kuwait and the Neutral Zone. The Cenozoic (Tertiary-Quaternary) sediments can be divided into two groups: the Kuwait Group and the Hasa Group. The Mesozoic (Late Cretaceous) sediments are characterized by carbonate rocks [3]. A generalized lithostratigraphic subdivisions of Tertiary-Quaternary sediments in Kuwait with the groundwater conditions [4] is summarized and discussed below.

1.3. The Kuwait Group

The Kuwait Group consists of sand, gravel, sandstone, clay, silt, calcareous and gypseous cemented sandstones, and marl covering the entire surface of Kuwait and extending down to the top of the underlying Dammam Formation. The thickness of the Kuwait Group increases from 150 m in the southwest to about 400 m in the northeast. The Kuwait Group is relatively dry in the extreme southwest and is almost saturated with water along the coast of the Arabian Gulf. In the north of Kuwait, the Kuwait Group can be divided into three formations based on the presence of an intermediate evaporite development. These divisions are Dibdibba, Lower Fars, and Ghar Formations, arranged from top to bottom. The undivided Kuwait Group extends under all of Kuwait with an extension eastwards beneath the Arabian Gulf. The Dibdibba Formation was named after the type locality Al-Dibdibba Plain, which extends from Basra to the northern part of Kuwait. The Dibdibba Formation is overlain by unconsolidated Recent and sub-Recent sediments of varying lithologies. The Lower Fars Formation ranges in thickness from 61 m in the west to more than 100 m in the eastern area into the offshore and it is absent in the south. It consists of fine to coarse-grained conglomeratic sandstone, variegated shale, and thin, fossiliferous limestone. The outcrop thickness of the Ghar Formation is only 33 m but it increases in subsurface and ranges from 195 to 250 m of marine to terrestrial, coarse-grained, unconsolidated sandstone with a few thin, sandy limestone, clay and anhydrite layers. At the base of the formation, above the eroded top of the Dammam Formation, is a brown, marly, coarse-grained sandstone with white, crystalline limestone resting unconformably over the Dammam Formation, and in gradational contact with the Lower Fars Formation.

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2. Hydrogeology

The northeastern part of Arabian Peninsula is characterized by four major systems of aquifers. These are (1) The Paleozoic-Triassic System, (2) The Cretaceous System, (3) The Eocene System, and (4) The Neogene-Quaternary System. The last two aquifers contain usable water, while the other deeper aquifers have connate water. Thus, the principle aquifer system in Kuwait consists of the Kuwait Group and the Dammam Formation of the Hasa Group. Many hydrological and hydrochemical evidences indicate local hydraulic connection between the Kuwait Group and the Dammam Formation aquifers in which both aquifers are considered as one complex system forming the main potential aquifers in Kuwait. Basically, the saturated part of the Kuwait Group and the Dammam Formation aquifers are replenished by infiltration on the outcrop area of Hasa Group at the eastern-northeastern part of Saudi Arabia and groundwater is discharged in Shatt Al-Arab and the Arabian Gulf [5]. Potentiometric level maps of the Kuwait Group and the Dammam Formation aquifers indicate a direction of groundwater movement from southwest to northeast direction. Due to the variations of clay percentage and cementation degree, the Kuwait Group is divided into two aquifers separated by an aquitard formation of clay and sand. Accordingly, the Kuwait Group appears to be semi-confined aquifer with a free water surface in the uppermost horizons. The saturated thickness of the Kuwait Group aquifer gradually increases toward northeast direction, as related to the structure of the Dammam Formation, where the groundwater in the aquifer becomes very saline.

The Kuwait Group aquifer is hydraulically connected with the underlying Dammam Formation aquifer under natural hydrological conditions; the flow occurs in a dynamic equilibrium state, in SW-NE direction, to be discharged finally by seepage into Kuwait Bay and the Arabian Gulf [6]. The Kuwait Group aquifer gains part of its water by leakage from the Dammam Formation aquifer. The other sources of aquifer replenishment are the infiltration through the well-developed wadies and depression system, and lateral flow coming from Saudi Arabia. It is generally estimated that the hydraulic conductivity in the aquifer conjunctively decreases with depth by the increase of cementation degree. The hydraulic conductivity is relatively high in the upper saturated zones of the aquifer.

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3. Objectives of the study

The main objectives of this piece of research are to identify the aquifer type and its characteristics, to reveal the geochemistry of the study area in order to recognize the prevailing and the major geochemical processes that control the quality of the groundwater. Moreover, to evaluate the suitability of groundwater for drinking and irrigation, physiochemical and irrigation parameters have been determined.

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4. Methodology

Seventy-one groundwater samples have been collected and analyzed to determine physical parameters like pH, EC, TDS, total hardness (TH), total alkalinity, and SiO2. In addition, the chemical parameters of the major cations and anions such as Ca2+, Mg2+, Na+, K+, HCO3, SO42−, and Cl expressed in mg/l were analyzed and converted to equivalent per million (e.p.m), and %e.p.m. [7]. Ion balance equation was applied to validate the accuracy of the chemical analyses where ±5% is acceptable [8]. The reaction error of all groundwater samples was less than the accepted limit of ±10% [9].

A speciation model has been used to determine the degree of saturation of groundwater with respect to some minerals using WATEQ4F program [10]. A mass-balance modeling WATEVAL computer program [11] is used to reveal the major geochemical reactions that control the geochemistry of the study area, along with the application of Gibb’s ratio to assess the functional sources of dissolved chemical constituents, and to recognize the main processes governing the groundwater chemistry of the study area [12]. Hydrochemical facies interpretation is used to determine flow pattern and origin of chemical histories of groundwater by plotting the major cations and anions on the Piper diagram [13]. The assessment of groundwater for irrigation purposes based on different irrigation indices is carried out which includes sodium adsorption ratio (SAR), residual sodium carbonate (RSC), %Na. permeability index (PI), potential salinity (PS), salinity hazard, magnesium ratio (MgR), Kelly’s ratio (KR), and chloro-alkaline index [14].

Wilcox diagram Wilcox [15] and Doneen permeability index [16, 17] have also been utilized for classification of groundwater for irrigation.

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5. Analyses and evaluation of pumping test data

A pumping test is a tool to determine the hydraulic characteristics of water-bearing formations such as transmissivity, storage coefficient, and any relevant hydrogeological properties. Such a test is called an aquifer test.

Analytical methods were applied to determine the aquifer type and hydrogeological properties of the Kuwait Group aquifer of the study area. These methods are Theis type curve [18], Cooper and Jacob straight line method for confined aquifer [19], and Walton method for semi-confined aquifer [20]. In effect, the pumping test data analyses indicated that the Kuwait Group aquifer is confined to semi-confined aquifer as shown in Figure 2 for the well AT-15 and Figure 3 for the well AT-18. The aquifer transmissivity ranges between 62.03 and 320.51 m2/day, where the estimated storage coefficient equals 7.5 × 10−4. The flow net analysis shows that the groundwater flows from the southwest to the northeast. Recharge to the aquifer is primarily from subsurface flow from adjacent bed rocks and by leakage from the underlying Dammam Formation aquifer. The presence of an aquitard layer (i.e., sandy clay) that bounds the aquifer from the top acts as a semipermeable layer and can leak water into the aquifer in the direction of the hydraulic gradient.

Figure 2.

Time-drawdown curve of well no. AT-15, using Cooper and Jacob straight line method.

Figure 3.

Time-drawdown curve of well no. AT-18, Walton method.

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6. Mechanisms of controlling groundwater chemistry

It is important to study the relationship between the water chemistry and the aquifer lithology. Gibbs as mentioned in [12] suggested a diagram that represents the ratio of dominant anions and cations plotted against the value of TDS. These ratios can be divided into two formulas, the first ratio is for the cations [(Na+ + K+)/(Na+ + K+ + Ca2+)] and the second ratio is for the anions Cl/ (Cl + HCO3) as a function of TDS. This diagram is widely used to evaluate the functional sources of dissolved constituents such as precipitation dominance, rock dominance, and evaporation dominance. The chemical analyses of the study area are plotted in Gibb’s diagram as shown in Figure 4, and they showed that the predominant samples fall into the category of rock-water interaction field and few samples are located in evaporation-dominance field and precipitation-dominance field, which revealed that the chemical weathering of rock-forming minerals is influencing the groundwater quality by dissolution of rock through which there is circulation, while the data in the evaporation-dominance field indicate that the increasing ions of Na+ and Cl are in relation with the increasing of the TDS, as evaporation will increase the concentration of total dissolved in groundwater.

Figure 4.

Gibbs plots represent groundwater chemistry and geochemical process in the study area.

6.1. Hydrochemical facies

Hydrochemical facies interpretation using Piper trilinear diagram is a useful tool for determining the flow pattern and origin of chemical histories of groundwater. The Piper trilinear diagram is presented in Figure 5. One principal hydrochemical water type has been delineated. The majority of the groundwater samples of the study area fall in Ca 2+– Na+ − Cl water type, where alkaline earth (Ca2+ + Mg2+) exceeds the alkaline (Na+ + K+) and strong acid (Cl and SO42−) exceeds the weak acid (HCO3 and CO32−), and non-carbonate hardness exceeds 50%.

Figure 5.

Piper trilinear diagram representing the chemical analysis of the study area.

6.2. Saturation index

Geochemical models are tools used to calculate chemical reaction in groundwater system such as dissolution and precipitation of solids, ion exchange, and sorption by clay minerals. In this study, the speciation model has been applied to the groundwater samples of Al-Atraf field to determine the saturation index (SI) of minerals. The SI for a given mineral measures the degree of saturation of that mineral with respect to the surrounding system. The degree of saturation index is defined as follows [21]:

SI=logKiapKspE1

where “iap” is the ion activity product of the dissociated chemical species in solution and “Ksp” is the solubility product of the mineral. When SI is <0, it indicates that the groundwater is undersaturated with respect to that particular mineral. When SI > 0, it means that the groundwater is being saturated with respect to the mineral and incapable of dissolving more of the minerals. The oversaturation can also be produced by incongruent dissolution, common ion effect.

Table 1 shows the saturation indices of anhydrite, calcite, gypsum, dolomite, halite, and silica along with Pco2. Nearly, all groundwater samples of the study area are undersaturated with respect to anhydrite, gypsum, halite, and silica and oversaturated with respect to calcite and dolomite.

Table 1.

Results of thermodynamic speciation calculation of the study area.

The partial pressure of the carbon dioxide value (Pco2) of the study area ranges between 1.32 × 10−3 and 8.23 × 10−3 atm., with an average value of 3.78 × 10−3 atm. This indicates that the groundwater of the Kuwait Group aquifer becomes charged with CO2 during infiltration through the soil zones. According to Appelo et al. [22], when Pco2 values range between 10−2.5 and 10−6.4 atm., it represents a closed system. Since the Kuwait Group aquifer is acting as a confined to semi-confined aquifer, it is more likely that the groundwater represents a deep, closed environment system. The mass-balance modeling as mentioned in Ref. [11] has been applied to specify the amounts of reacting minerals and to determine the possible source of the major ions in a specific groundwater system. This is in order to deduce groundwater source rock and to determine the nature and the extent of the geochemical reactions that occur in this system, that is, water-rock interaction. By the application of Hounslow concept, all groundwater samples of the study area showed that Cl > Na+ indicating that the reverse ion exchange is likely to occur in aquifer. The ratio Ca2+ / Ca2+ + SO42− of most groundwater samples ranged between 0.41 and <0.5 indicating calcium removed by ion exchange or calcite precipitation, and few groundwater samples show a range value of 0.5–0.6, which is due to gypsum dissolution. According to reference [11], waters with HCO3/SiO2 < 5 indicated mainly silicate weathering. However, the ratio HCO3/SiO2 of the groundwater samples found to be ranged between 1.45 and 4.77 which indicate that silicate weathering is a dominant chemical process in the aquifer. Dissolved silica data show the influences of silicate weathering on water chemistry in the study area. Participation of silicate minerals in the chemical reactions plays a vital role in groundwater chemistry. Silicate weathering can be evaluated by estimating the ratio between Na+ + K+ and the total cation (e.p.m) as shown in Figure 6a. This reveals that the silicate weathering contributes mainly Na+ and K+ ions to groundwater [23]. Further, the plot of Ca2+ + Mg2+ versus total cations of the groundwater samples as in Figure 6b has a linear spread, indicating that some of these ions (Ca2+ + Mg2+) are resulted from the weathering of silicate minerals. In addition, all the groundwater samples exhibited an oversaturation with respect to calcite, which suggest the prevailing of calcite precipitation process in the aquifer.

Figure 6.

(a) Relation between total cations and (Na+K) in the study area. (b) Relation between total cations and (Ca+Mg) in the study area.

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7. Geochemical evolution of groundwater

The initial composition of groundwater originates from rainfall with low concentrations of dissolved ions. During its return path to the ocean, the water composition is altered by rock weathering and evaporation causing more Ca2+, Mg2+, Na+, SO42−, HCO3, Cl, and SiO2 to be added. The concentration of these ions depends on the rock mineralogy that the water encounters and its rapidity along the flow path. The abundance of the major cations in Al-Atraf field is in the order of Na+ > Ca2+ > Mg2+ > K+. The sequence of the anions is in the order of Cl > SO42− > HCO3. The majority of the groundwater samples of the study area (75.36%) exhibited NaCl water chemical type, followed by (23.19%) of Na2SO4 and (1.45%) of CaSO4 water chemical types. The average TDS of 4441 mg/l represents brackish groundwater as presented in Table 2. Calcium and magnesium present in the groundwater are mainly due to the dissolution of gypsum and anhydrite, the most rock-forming minerals of the Kuwait Group aquifer of the study area. Calcium ions are derived also from cation exchange process. The concentration of calcium ions in the study area ranges from 332 to 743 mg/l with an average value of 484.23 mg/l and magnesium ranges from 85 to 203 mg/l, with an average value of 140.87 mg/l. This indicates that the Ca2+ ion concentration in the study area is relatively higher than magnesium ion. Alkalinity is the quantitative capacity of an aqueous solution to neutralize an acid. The ideal range of the total alkalinity is from 80 to 140 mg/l. In natural environment, carbonate alkalinity tends to make up most of the total alkalinity due to the common occurrence and dissolution of carbonate rocks and the presence of carbon dioxide in the atmosphere. The total alkalinity of the study area ranges between 51.2 and 127 mg/l as CaCO3 with an average value of 91.39 mg/l. Figure 7a represents Ca2+ + Mg2+ versus alkalinity + SO42− in e.p.m., suggesting that these ions have resulted from weathering of carbonate and sulfate minerals (gypsum and anhydrite). However, most of the points are placed in Ca2+ + Mg2+ side, which indicates excess calcium and magnesium derived from other processes such as reverse ion exchange reactions. In Ca2+ versus alkalinity diagram, Figure 7b indicates the contribution of both calcite and dolomite weathering on groundwater chemistry of the study area. Moreover, in Ca2+ versus SO42− diagram (Figure 7c), most of the sample show excess calcium over sulfate, which reveal that the groundwater samples seem to be derived from gypsum or anhydrite dissolution. Moreover, excess sulfate over calcium in few samples expresses the removal of calcium from the system likely by calcite precipitation. Therefore, silicate weathering and carbonate dissolution are the prevailing geochemical processes in the aquifer of the study area.

Figure 7.

(a) Relation between Ca+Mg and alkalinity + SO4. (b) Relation between Ca2+ and alkalinity. (c) Relation between Ca2+ and SO2−4.

7.1. Ion exchange

Ion exchange is one of the important processes responsible for the concentration of ions in groundwater.

CAI1=ClNa++K+ClE2

Where all values are expressed in meq/l. When there is an exchange between Ca2+ or Mg2+ in groundwater with Na+ and K+ in the aquifer material, the CAI-1 is negative, and if there is a reverse ion exchange, CAI-1 will be positive [24]. The values of CAI-1 of the study area are positive in most wells, and very few wells show negative, and the CAI-1 ranges from −0.05 to 0.39 with an average value of 0.19 as presented in Table 3. Thus, it reveals that reverse ion exchange is the dominant process in the groundwater, whereas normal ion exchange is also noticed in a very few wells.

Table 2.

Report of physico-chemical parameters of the studied groundwater samples of the study area.

Table 3.

Irrigation water quality parameters for groundwater samples of the study area.

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8. Drinking and irrigation water quality

The assessment of suitability of the groundwater for drinking and irrigation purposes can be determined through the parameters such as EC, TDS, pH, SAR, %Na, RSC, Kelley’s ratio, MgR, CAI-1, P.I, and P.S as displayed in Table 3.

8.1. Drinking water quality

The suitability of the groundwater in the study area is evaluated for drinking by comparing with the standard guideline values [25]. According to WHO specifications, TDS up to 500 mg/l is the highest desirable and up to 1500 mg/l is the maximum permissible level. Based on this classification, the TDS of the groundwater of the study area ranges between 3504 and 6366 mg/l with an average value of 4441 mg/l, which exceeds the recommended limit. However, the major cations and anions composition of the study area are all above the standard guideline of the WHO for drinking purposes. Water hardness causes more consumption of detergents at the time of cleaning, and some evidences indicate its role in heart disease [26]. The total hardness was determining by the following equation according to [27]:

TH=2.5Ca2++4.1Mg2+.E3

where Ca2+ and Mg2+ concentrations are expressed in mg/l as CaCO3. Hardness of water is due to the precipitation of Ca2+ and Mg2+ salts like carbonate, sulfates, and chlorides. Hardness of water causes scaling of pots, boilers, and irrigation pipes. However, the total hardness of the study area is varying from 1326 to 4040 mg/l as CaCO3, with an average value of 1826.22 mg/l as shown in Table 2. The analytical result of TH indicates that the groundwater of the study area is exceeding very hard water type according to [28] as shown in Table 4. Therefore, according to TDS and TH standards the groundwater is not suitable for drinking purposes.

Table 4.

Water classes (After [28]).

8.2. Irrigational suitability

The suitability of groundwater for irrigation depends on the effect of mineral composition of water on the soil and plants. The effect of the salt on soils causes change in soil structure, permeability, and hence it effects on plant growth.

8.2.1. Residual sodium carbonate

Residual sodium carbonate has been calculated to determine the hazard effects of carbonate and bicarbonate on the quality of water for irrigation and is expressed by the equation:

RSC=HCO3+CO32Ca2++Mg2+E4

Where all ionic concentrations are expressed in meq/l. The classification of irrigation water according to the RSC presents in Table 5 after [29], where water containing more than 2.5 meq/l of RSC are not suitable for irrigation, while those having <1.25 meq/l are good for irrigation. Eaton (1950) indicated that if waters which are used for irrigation contain excess of HCO3 + CO32− than its equivalent Ca2+ + Mg2+, there will be a residue of Na+ + HCO3 when evaporation takes place and the pH of the soil increases up to 3 [30]. When total carbonate levels exceed the total amount of calcium and magnesium, the water quality diminished [31]. The calculated RSC values of the groundwater samples of the study area are ranged from −52.63 to −24.52 meq/l with an average value of −34.31 meq/l. Negative RSC indicates that sodium buildup is unlikely, since sufficient calcium and magnesium are in excess of what can be precipitated as carbonates [32]. Hence, the groundwater of the study area is safe for irrigation.

Table 5.

Water classes based on RSC (after [29]).

8.2.2. Permeability index

The permeability of soil is affected by long-term use of irrigation water and is influenced by sodium, calcium, magnesium, and bicarbonate contents in soil. Doneen (1964) set a criteria for assessing the suitability of water for irrigation based on permeability index; accordingly, waters can be classified as Class I, Class II, and Class III. The Class I and Class II waters are suitable for irrigation with 50–75% or more of maximum permeability, whereas Class III water is unsuitable with 25% of maximum permeability. Therefore, soil permeability is affected by consistent use of irrigation water which increases the presence of sodium, calcium, magnesium, and bicarbonate in the soil [33].

The permeability index is used to measure the suitability of water for irrigation purpose when compared with the total ions in meq/l, and it is expressed as follows:

PI=Na++HCO3Ca2++Mg2++Na+100E5

In the present study, the P.I of the groundwater samples ranged from 37.86 to 56.63% with a mean value of 49.1%, and it is observed that all the groundwater samples fall in Class II category of Doneen Chart (Figure 8). Therefore, the groundwater of the study area is good for use in irrigation.

Figure 8.

Permeability index diagram of the study area.

8.2.3. Potential salinity

Doneen as in Ref. [17] introduced an important parameter “Potential Salinity” for assessing the suitability of water for irrigation uses, which defined as chloride concentration plus half of the sulfate concentration expressed in meq/l.

Potential salinity = Cl + ½ SO42−. On the basis of the potential salinity, Doneen [17] subdivided the irrigation water into three classes as presented in Table 6. The potential salinity of the majority of the analyzed groundwater samples of the study area ranges between 36.55 and 83.56 meq/l with an average value of 54.17 meq/l, indicating high values of potential salinity. However, it is found that the classification of the groundwater of the study area for irrigation purposes fall in Class III; therefore, the groundwater should be used in case of a soil of high permeability.

Table 6.

Classification of irrigation water based on potential salinity.

8.2.4. Sodium adsorption ratio

Sodium concentration is considered an important factor to express reaction with the soil and reduction in its permeability. Therefore, sodium adsorption ratio is considered as a better measure of sodium (alkali) hazard in irrigation water as it is directly related to the adsorption of Na+ on soil and is the important criteria for estimating the suitability of the water for irrigation. SAR can be computed as follows:

SAR=Na+Ca2++Mg2+2E6

Where all ionic concentrations are expressed in meq/l. The SAR of the study area ranges between 4.65 and 9.4, with an average value of 7.54. The SAR values of all the study area are found to be <10 and are classified as categories S1 and S2, as low and medium sodium water, respectively. Therefore, based on the sodium hazard class the groundwater of the study area is suitable for irrigation.

8.2.5. Salinity hazard

The most important criteria regarding salinity and water availability to the plant is the total salt concentration. Since there exists a straight line correlation between electrical conductivity (EC) and total salt concentration of waters, the most expedient procedure to evaluate salinity hazard is to measure its electrical conductivity measured in (μmohs/cm) [34]. On the basis of salt concentration, the US Salinity Laboratory Staff divided the irrigation waters into four classes. Later on, another class was added to it [35] as given in Table 7. Waters having EC values above 1500 μmohs/cm can cause serious damage.

Table 7.

Classification of waters based on EC [35].

For rating irrigation waters, the US salinity diagram was used, in which the SAR is plotted against EC as shown in Figure 9, where the EC values of samples of the study area range from 4370 to 8230 with an average value of 5837 μmohs/cm and water exhibited very high to extensively high water salinity and medium sodium, high sodium type (C4-S2, C4-S3). Few samples are located on C4-S4 type. Therefore, the groundwater can be used with tolerant crops of clayey, sandy loam, and loamy sand soil texture, and special management for salinity control.

Figure 9.

Wilcox diagram illustrating the groundwater quality of the study area.

8.2.6. Magnesium ratio

In most waters, calcium and magnesium maintain a state of equilibrium. A ratio namely index of magnesium hazard was developed by [36]. According to this, a high magnesium hazard value of >50% has an adverse effect on the crop yield as the soil becomes more alkaline, and effect on the agricultural yield, and a harmful effect on soil will appear.

Mgratio=Mg2+Ca2++Mg2+×100E7

Where all ionic concentrations are expressed in meq/l.

In the study area, the magnesium hazard values fall in the range value of 25.65–40.46% with an average value of 32.48%, that is, magnesium hazard ratio is <50%, which is recognized as suitable for irrigation.

8.2.7. Sodium percentage (%Na)

Sodium is an important ion used for the classification of irrigation water due to its reaction with soil, reduces its permeability. The %Na is computed as:

%Na+=Na+K+Ca2++Mg2++K++Na+×100E8

Where all ionic concentrations are expressed in meq/l. According to [15], in all natural waters, %Na+ is a common parameter to assess its suitability for irrigation purpose as shown in Table 8. If the concentration of Na+ is high in irrigation water, Na+ gets absorbed by clay particles, displacing Mg2+ and Ca2+ ions. This exchange process of Na+ in water for Ca2+ and Mg2+ in soil reduces the permeability of soil and eventually results in poor internal drainage of the soil, and such soils are usually hard when dry [37]. The values of %Na+ of the study area varies from 35.28 to 54.23% with an average value of 46.73% which fall in good to permissible category, showing that the groundwater of the study area is suitable for irrigation; meanwhile, the EC ranges between 4370 and 8230 μmohs/cm, in which the groundwater salinity is classified as very extensively high as presented in Figure 10; therefore, the groundwater can be used for irrigation under specific conditions.

Table 8.

Classification of groundwater based on %Na [15].

Figure 10.

A plot of percentage of sodium vs. electrical conductivity of groundwater of the study area.

8.2.8. Kelly’s ratio

Kelly’s ratio is used for the classification of water for irrigation purposes. A Kelly’s index (>1) indicates an excess level of sodium in waters [38]. Therefore, water with a KR (<1) is suitable for irrigation. KR is calculated by using the formulae, where all the ions are expressed in meq/l.

Kellysratio=Na+Ca2++Mg2+E9

The values of the KR in the present study varied between 0.55 and 1.2 with an average value of 0.89 which is <1. It is found that 87.32% of the groundwater samples have KR <1, and 12.68% KR > 1. Accordingly, the groundwater of the study area is suitable for irrigation.

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9. Conclusion

The study area is located in the southwest of Kuwait. It includes 83 wells that produce brackish groundwater from Kuwait Group aquifer. Pumping test analyses revealed that the aquifer is acting as a confined to semi-confined aquifer, and transmissivity ranges between 62.03 and 320.51 m2/day and increases toward N-NE. The estimated storage coefficient is 7.5 × 10−4.

In the present study, the pH values range from 7 to 7.9, indicating an alkaline type of groundwater. The total alkalinity ranges from 51.2 to 127 mg/l with an average value of 91.39 mg/l. The electrical conductivity values range from 4370 to 8230 μmohs/cm with an average value of 5837 μmohs/cm. Total dissolved solids vary from 3504 to 6366 mg/l, with an average value of 4441 mg/l representing brackish groundwater. The majority of the groundwater samples of the study area exhibited NaCl water chemical type, followed by Na2SO4, and CaSO4 water chemical types, respectively.

The groundwater is very hard, where the average TH is 1826 mg/l as CaCO3. The sequence of the abundance of the major cations and anions is Na+ > Ca2+ > Mg2+ > K+ and Cl > SO42− > HCO3. The dominant hydrochemical facies of the groundwater in the study area is Ca-Na-Cl. According to Gibb’s plot, most of the samples of the study area are under the category of rock interaction and few samples are found to have the category of evaporation. Few samples fall in the precipitation-dominance area suggesting the influence of precipitation on the groundwater. Silicate weathering is the dominant weathering process in the study area; however, the carbonate weathering processes are also responsible for the supply of some ionic species to the groundwater. The calculation of the saturation indices revealed that the groundwater is oversaturated with respect to calcite and dolomite and undersaturated with respect to gypsum, anhydrite, halite, and SiO2.

The positive index of base exchange for most of the samples (>98%) indicates that there exists a chloro-alkaline equilibrium, and there is an ion exchange of Na+ and K+ from water with magnesium and calcium in the rock, except one well, where the value is negative, revealed cation-anion exchange (chloro-alkaline disequilibrium).

Most of the TDS and TH values obtained are beyond the permissible limits making the groundwater of the study area unsuitable for drinking and for various domestic activities.

The suitability of groundwater for irrigation was evaluated based on the irrigation quality parameters like RSC, permeability index, potential salinity, SAR, salinity hazard, magnesium ratio, %Na, and Kelley’s ratio. The majority of the groundwater samples exhibited very high salinity to extensively high water salinity class, medium and high sodium water type, respectively, According to the values of these parameters, the groundwater of the study area was found to be used for irrigation under high soil permeability, good drainage, and plants with good salt tolerance should be selected.

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Acknowledgments

The author would like to thank the Ministry of Electricity and Water for providing the chemical and pumping test data of Al-Atraf field.

References

  1. 1. Milton DI. Geology of the Arabian Peninsula, Kuwait. Geological Survey Professional Paper 560-F. U.S Government Printing Office, Washington, U.S.A; 1967. pp. 1-7 F
  2. 2. Fuchs W, Gattinger TE, Holzer HF. Explanatory Text to the Synoptic Geologic Map of Kuwait. A Surface Geology of Kuwait and the Neutral Zone. Vienn: Geological Survey of Austria; 1968. 87 pp
  3. 3. Al-Sharhan AS, Nairn AE. Sedimentary Basins and Petroleum Geology of the Middle East. Amsterdam, Netherlands: Elsevier Science B.V; 1997. p. 843
  4. 4. Besharah J, Al-Saad A. Oil Lakes Formation and Means of Remediation, Petroleum, Petrochemicals and Materials Division. Unpublished report. Kuwait Institute for Scientific Research, Kuwait; 1992
  5. 5. Omar SA, Al-Yaqubi AS, Senay Y. Geology and groundwater hydrology of the State of Kuwait. Journal of the Gulf and Arabian Peninsula Studies. 1981;1:5-51
  6. 6. Al-Ruwaih FM, Al-Awadi E. Groundwater utilization and Management in the State of Kuwait. Water International. 2000;25(3):378-389
  7. 7. Fetter WC. Applied hydrogeology. 4th ed. Prentice-Hall, Inc; 2001. 598pp
  8. 8. Saether OM, De-Caritat P. Geochemical processes, weathering and groundwater recharge in catchments. Balkema, Rotterdam. The Netherlands; 1997. 400pp
  9. 9. Hem JD. Study and Interpretation of Chemical Characteristics of Natural Water. 3rd ed. Jodhpur, India: Book 2254: Scientific publ; 1991
  10. 10. Ball JW, Nordstrom DK. Geochemical Model to Calculate Speciation of Major, Trace and Redox Elements in Natural Waters. Report, U.S. U.S.A: Geological Survey, International Groundwater Modeling Center; 1992
  11. 11. Hounslow AW. Water Quality Data. Analysis and Interpretation. New York: Lewis Publishers; 1995
  12. 12. Gibbs RT. Mechanisms controlling world's water chemistry. Science. 1970;170:1088-1090
  13. 13. Piper AM. A graphical procedure in geochemical interpretation of water analyses. Transactions of the American Geophysical Union. 1953;25:914-923
  14. 14. Al-Ruwaih FM, Shaflullah GS. Geochemical processes and assessment of irrigation water quality using GIS for Al-Shagaya Field-C, Kuwait. International Journal of Environment, Agriculture and Biotechnology (IJEAB). 2017;2(1):165-180
  15. 15. Wilcox LV. Classification and Use of Irrigation Waters. Washington. D.C: US Department of Agriculture; 1955. 19pp
  16. 16. Doneen LD. In: Davis CA, editor. Notes on Water Quality in Agriculture. Water Science and Engineering, University of California; 1964
  17. 17. Doneen LD. The influence of crop and soil on percolating water. Proceedings of Groundwater Recharge Conference. California, U.S.A. 1961
  18. 18. Theis CV. The relation between the lowering of the Piezometric surface and the rate and duration of discharge of a well using groundwater storage. Transactions of the American Geophysical Union. 1935;25:519-524
  19. 19. Cooper HH, Jacob CE. A generalized graphical method for evaluating formation constants and summarizing well-field history. Transactions of the American Geophysical Union. 1946;27:526-534
  20. 20. Walton WC. Groundwater Resources Evaluation. Tokyo, Japan: McGraw Hill Book Company; 1970. 664 P
  21. 21. Deutsch WJ. Groundwater Geochemistry: Fundamentals and Applications to Contamination. U.S.A: Lewis Publishers, New York; 1997. 221pp
  22. 22. Appelo CAJ, Postma D. Geochemistry, Groundwater and Pollution. Rotterdam, The Netherlands: Balkema; 2005. 649pp
  23. 23. Stallard RF, Edmond JM. Geochemistry of the Amazon, the influence of geology and weathering environment on the dissolved load. Journal of Geophysical Research. 1983;88:9671-9688
  24. 24. Schoeller H. Geochemistry of groundwater. In: groundwater Studies- An international guide for research and practice (ch. 15, p.p. 1-18). Paris: UNESCO; 1977
  25. 25. WHO, editor. Guidelines for Drinking-Water Quality [Electronic Source]: Incorporations. 3rd ed. Geneva: WHO; 2008. 515pp
  26. 26. Schroeder HA. Relations between hardness of water and death rate from certain chronic and degenerative diseases in the United States. Journal of Chronic Diseases. 1960;12:586-591
  27. 27. Todd DK, Mays LW. Groundwater Hydrology. 3rd ed. John Wiley & sons, Inc; 2005. 636 pp
  28. 28. Sawyer GN, McCarthy DL. Chemistry of Sanitary Engineers. 2nd ed. New York: Mc Grow Hill; 1967. 518pp
  29. 29. Richards LA. Diagnosis and improvement of saline and alkaline soils. In: US Department of Agriculture Hand Book. 1954. 60pp
  30. 30. Eaton EM. Significance of carbonate in irrigation water. Soil Science. 1950;69:12-133
  31. 31. Sundaray SK, Nayak BB, Bhatta D. Environmental studies on river waters quality with reference to suitability for agricultural purposes: Mahanadi river esturarine system. India- a case study, Environmental Monitoring and Assessment. 2009;155:227243
  32. 32. Satyanarayanan M, Balaram V, Al Hussin MS, Al Jemaili MA, Rao TG, Mathur R, Dasaram B, Ramesh SL. Assessment of groundwater quality in structurally deformed granitic terrain in Hyderabad, India. Environmental Monitoring and Assessment. 2007;113:117-127
  33. 33. Chandu SN, Subbarao NV, Prakash SR. Suitability of groundwater for domestic and irrigation purposes in some part of Jhansi District, U. P. Bhujal Newa. 1995;10(1):12-17
  34. 34. Chhabra R. Soil Salinity and Water Quality. U.S.A.: A.A. Balkema Publishers; 1996. 284pp
  35. 35. Handa BK. Groundwater pollution in India. In: Proceedings of National Symposium on Hydrology. IAHS, publ. Univ. Roorkee, India. 1969. pp. 34-49
  36. 36. Paliwal KV. Irrigation with Saline Water. Monogram No.2 (new series). New Delhi: I A R I; 1972. 198pp
  37. 37. Saleh A, Al-Ruwaih FM, Shehata M. Hydrogeochemical processes operating within the main aquifers of Kuwait. Journal of Arid Environments. 1999;42:195-209
  38. 38. Kelly WP. Alkali Soils- their Formation Properties and Reclamation. 3rd ed. New York, U.S.A: Reinhold publication; 1951. 92pp

Written By

Fawzia Mohammad Al-Ruwaih

Submitted: 15 May 2017 Reviewed: 10 October 2017 Published: 20 December 2017