The steps followed, in this research, are resumed in Fig. 6.
Hydrochemical data
A statistical view of hydrochemical parameters (min, max, and standard deviation) is given in Table 2. The pH data ranged from 7.15 to 8.45 and 7.63 to 8.24 for the shallow and the deep samples, respectively. These results show that the both aquifers have a pH close to neutrality with a slight tendency toward the basic composition. The temperatures are characterized by heterogeneous values varying from 10.3 to 24.8 °C and 13.1 to 30.2 °C for the shallow and the deep samples, respectively. The temperature of water depends on the well depth, with an average value and standard deviation equal to 17.9 °C and 3.97 °C, for the shallow and springs samples, and equal to 22.8 °C and 4.96 °C for the deep samples. For the shallow and springs samples, the electrical conductivity values vary from 1544 to 9770 μs/cm with a mean of 2685 μs/cm. For the deep samples, the EC varies from 393 to 3960 μs/cm with a mean of 1729 μs/cm.
Table 2 Statistical summary of the physical and chemical parameters of HJB samples (ionic contents in mg/l) For the both type of samples (shallow/springs and deep), the chemical analysis indicated that the abundance order of the major cations is Na > Mg > Ca > K. For the shallow and springs samples, the concentration of major cations, Na+, Ca2+, Mg2+, and K+, are ranged from 142.6 to 1075, 37.8 to 70.4, 41.8 to 148.23, and 4.68 to 19.89 mg/l with a mean value of 265.54, 47.2, 84.38, and 7.61 mg/l, respectively. For the deep samples, the cations, Na+, Ca2+, Mg2+, and K+, are ranged from 17.48 to 459.31, 5.8 to 55.6, 0.47 to 117.67, and 2.34 to 15.6 mg/l with a mean value of 138.35, 37.7, 35.53, and 4.88 mg/l, respectively. The order of abundance of anion is Cl > HCO3− > SO4. The abundance of these cations and anion is derived from a mineralization process, which can be natural or anthropogenic.
The groundwater salinity shows a wide variation from 100 to 1800 mg/l with a mean value equal to 700 mg/l and from 700 to 6500 mg/l with a mean value equal to 1400 mg/l for the deep and the shallow aquifers, respectively. The distribution of the salinity presented in Fig. 7 reveals that in the shallow, aquifer has high soluble salts in the totality of samples (one sample, salinity < 1 and 13 samples, salinity > 1 g l−1 with one sample exceeding 6 g l−1) (Fig. 7). The deep aquifer has moderate salinity: 3 samples exceeding 1 g l−1 and the rest (11 samples) indicate salinity less than 1 g l−1. The high salinity values would be related to the leaching of salts from soils, the use of fertilizers in agriculture activities, or/and return flow from irrigation water (Mnassri et al. 2018). This hypothesis is confirmed by analyzing the samples that are taken from wells located in the irrigated perimeters (see Fig. 5).
Groundwater mineralization processes
Correlation of parameters
The correlation matrix of the shallow and springs samples indicated that the contents of sodium, magnesium, chloride, and calcium are high positively correlated with salinity (Table 3(a)). These positive correlations indicate the continuous addition of these ions along groundwater flow path. Therefore, these elements contribute to the groundwater mineralization. The concentration of Cl− is correlated with Na+ with a correlation index of 0.95, indicating that the halite dissolution may be the important reaction affecting the water chemistry. The electrical conductivity also shows a perfect positive correlation with Na+ (R = 0.98), Ca2+ (R = 0.82), salinity (R = 0.98), Cl− (R = 0.95), and moderately positive correlation with Mg2+ (R = 0.67).
Table 3 Pearson correlation matrix of HJB. (a) Shallow wells/springs, and (b) deep wells. Italics indicates significant 50% confidence level The matrix of the deep samples (Table 3(b)) indicates that EC shows a high correlation (positive) with salinity (R = 0.98), Na+ (R = 0.97), and Cl− (R = 0.96) and moderately positive correlation with Ca2+, Mg+, K+, and HCO3− with correlation value equal to 0.77, 0.75, 0.72, and 0.61, respectively. Na+ also shows a high correlation index (positive) with all the major ions except SO42−. The high correlation observed between some parameters suggests the extent of interdependence and also suggests that these ions may be derived from a common source.
Identification of water-rock interaction
To understand the main mechanisms governing groundwater chemistry, Gibbs’ diagrams have been used. The weight ratios of ratio I: (Na+/(Na++Ca2+)) and ratio II: (Cl−/(Cl− + HCO3−)) are plotting as a function of total dissolved solids (TDS), representing Gibbs’ diagrams. This diagram is used to identify the origin of dissolved constituents, such as rock weathering dominance, precipitation dominance, and evaporation dominance or by combination of these influences (Gibbs 1970). According to the Gibbs’ diagrams (Fig. 8), the data indicates that the chemical composition’s HJB samples are governed by evaporation and rock weathering. The importance of evaporation processes and rock weathering are also confirmed by the calculation of Hounslow ratio (Cl−/Σ anions) which indicates, for the both aquifers, two chemical sources: evaporate or brine water sources (ratios > 0.8 and TDS > 500) and rock weathering (ratios < 0.8) (Hounslow 1995).
A plot of Ca2+ and SO42− shows that for the shallow samples (Fig. 9a), one sample below the line 1:1 (PS 3) indicates a deficit in Ca2+, suggesting carbonate precipitation; two samples (PS10 and S1) are close to the bisector line (1:1), indicating that gypsum is the source of calcium, while the majority of samples are located above the dissolution straight line and indicated an excess in Ca2+, suggesting carbonate dissolution (Fig. 9a). For the deep samples, two samples (F11 and F14) are close to the bisector line (1:1), indicating that gypsum is a source of calcium, while the majority of the water samples are located above the dissolution straight line and indicated an excess in Ca2+, suggesting carbonate dissolution (Fig. 9a).
Evaporation process is also a major process in controlling the groundwater’s chemistry. The both type of samples (shallow/springs and deep) represented in Fig. 9b are very close to the bisector line (1:1) of sodium against chloride’s plot, suggesting that in these wells, salinity is controlled by halite dissolution.
According to scatter diagrams (Fig. 9c), the groundwater mineralization is controlled, in addition to minerals dissolution, by ion exchange with clay minerals present in the aquifers and also reverse ion exchange.
The indicator of carbonate and silicate weathering is confirmed by the (Ca2++Mg2+) against (HCO3− + SO4 2−) scatter diagrams in Fig. 9d showing that:
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The shallow and springs samples are distributed at the left and the right part of the 1:1 (line). One sample indicating the abundance of SO4 2− + HCO3− by 54% over Ca2++Mg2+ is a sign of silicate weathering. The most of samples located in the left part of the 1:1 (line) indicates that the water samples are related to carbonate rock.
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The deep samples are distributed at the left part of the 1:1 (line) indicating a weathering of carbonates which represents the main source of bicarbonate ion.
Hydrochemical water type
Considering the piper trilinear plot (Figs. 10 and 11), we can distinguish three major groundwater groups for the deep aquifer: Na-Cl, Ca-Mg-Cl, and Ca-Cl and two water type for the shallow aquifer: Na-Cl and Ca-Mg-Cl. For the deep aquifer; the first group (Ca-Cl) type waters are highly mineralized. They represent the northwest part of Beglia aquifer (recharge zone). The high Ca+ concentration in the northwest part of Beglia aquifer is derived from dissolution of carbonate present in the cretaceous of Dj Mghilla. The second water type is Na-Cl; it presents 78% of samples for the deep aquifer and also for the shallow aquifer. The Na cation is derived from the ion exchange with the clay of the adjacent layer (Saouaf formation). Two much closed wells, in the deep aquifer, present two different water type (Na-Cl and Ca-Mg-Cl); the Na-Cl water type presents 78% of samples while Ca-Mg-Cl is present only in one sample. Based on the screen position of wells, we can detect that the well corresponding to the Ca-Mg-Cl water type presents very different screen position; so, we can conclude that Beglia aquifer presents vertical water-type stratification.
The chemical data of shallow/springs and deep samples, collected from the studied area, are plotted in the Chadha diagram presented in Figs. 10 and 11. All the samples fall in fields 6 and 7, and this means that “alkaline earths exceed alkali metals and strong acidic anions exceed weak acidic anion” and “Alkali metals exceed alkaline earths and strong acidic anions exceed weak acidic anions.”
Multivariate statistical analyses
Principal component analysis was achieved for the two aquifers separately: a dataset of 28 samples (14 deep samples and 14 shallow and springs samples) and 12 physico-chemical elements to determine relationships between major elements and also physical parameters. Table 4 shows the eigenvalues, the percentage of variance, associated with each other, and the cumulative percentage.
Table 4 Variance explained by the first three principal components The results of the analysis presented in Fig. 12 reveal that the first three factors illustrate approximately 78%, of total variance, for the shallow and springs samples and 86% for the deep samples. For the shallow and springs samples, the first factor is responsible for about 48%, of total variance, and is well represented by salinity, Na+, EC, Mg, Ca2+, and Cl−. These elements ensure the mineralization of the shallow aquifer’s water. Consequently, component “1” is defined as the salinity component representing the weathering of halite and evaporate minerals. Component “2” is represented by O2, SO42−, and HCO3−. Additional 12.25%, of total variance, was explained in F3 and was represented by K+, O2, and pH.
For the deep samples, the first factor is responsible for about 63.11%, of total variance, and is well represented by Mg2+, salinity, Na+, K+, Ca2+, HCO3−, Cl−, and EC; this component is defined as the salinity component representing the weathering of halite and evaporate minerals. Component 2 is represented by SO42− defined as a factor of sulfates. The third component represents 10.85%, of total variance, was explained in F3, and was represented by O2 and pH.
Water quality
Drinking use
Standard limits
The physical (pH and EC (μs/cm)) and chemical parameters (K+, Ca+, Mg+, Cl−, SO2−, Na+, HCO3−/in mg/l) were compared with the world’s standard (WHO 2011) and the national standard (NT 2013). As show in Fig. 13, all samples (n = 28) respect the maximum permissible limit, for the both WHO and NT standards, for the pH, the potassium (K+), the calcium (Ca+), the magnesium (Mg+), the bicarbonates (HCO3−), and the sulfates (SO2−). For the electrical conductivity (EC), the limit given by the WHO (1500 μs/cm) is not respected by all the shallow samples and the most of deep samples (58%). For the chlorides (Cl−), all the shallow samples exceeded the WHO limit (250 mg/l) and 29% of the shallow samples exceeded the national limit (600 mg/l). For the deep aquifer, 9 samples (64%) exceeded the WHO limit and two samples (14%) exceeded the national limit (600 mg/l). For the sodium (Na+) parameter, the permissible value given by the WHO (200 mg/l) was respected only by four samples (29%) in the shallow aquifer and exceeded by three samples (21%) from the deep one. In all collected samples, only one physical parameter and two major ions (one cation and one anion) not respect the WHO and NT limit in the most of samples. In the total, only 15% of samples respect the permissible limits, of all physico-chemical parameter, given by the WHO, which can affect the human health.
Water quality indices
The evaluation of water quality, of HJB, for drinking uses was effectuated using three quality indices: EWQI, WQI, and ImpWQI.
The WHO standards were selected to calculate the quality rating scale (Q). The WQI ranged from 64.41 to 328.64 for the shallow aquifer and from 22 to 155.61 for the deep aquifer. It shows four classes of both aquifers (Table 5), extended from “good” to “extremely poor” for the shallow aquifer and from “excellent” to “poor” for the deep one. For the EWQI, the index value ranged from 55.29 to 248.41 for the shallow aquifer and from 22 to 122.8 for the deep aquifer. It shows three classes of both aquifers (Table 5, extended from “good” to “extremely poor” for the shallow aquifer and from “excellent” to “Medium” for the deep one. For the ImpWQI, the value ranged from 178.69 to 1011 for the shallow aquifer and from 43.93 to 475.6 for the deep aquifer. It shows various classes of both aquifers (Table 5), extended from “poor” to “extremely poor” for the shallow aquifer and from “excellent” to “poor” for the deep one.
Table 5 Classification of shallow and deep samples quality based on EWQI, WQI, and ImpWQI A correlation was effectuated between the physico-chemical parameters, used in the calculation of the indices, and the three indices (Table 6). For the both aquifers, the three indices (ImpWQI, EWQI, and WQI) present a negative low correlation with the pH, a low correlation with sulfates (SO4−), and a strong correlation with the major physico-chemical parameters (EC, Na+, Ca2+, Mg2+, Cl−, HCO3−) except in the shallow aquifer the potassium K+ and the bicarbonates HCO3− present a low correlation value with the three indices (Table 6). The correlation values are related to the parameter’s weight which is given in WQI method and calculated in the two indices (ImpWQI and EWQI). For the both types of samples (shallow/deep), the three indices indicate very similar correlation values but the EWQI indicate the high values with very negligible differences with the two other indices.
Table 6 Correlation between the various water quality indices (ImpWQI, EWQI, and WQI) and physico-chemical parameters for the deep and shallow aquifer Figure 14 shows the water quality index values calculated by the three proposed indices (WQI, ImpWQI, and EWQI) in the deep and shallow aquifers. The indices showed similar results, regarding EWQI and WQI. The ImpWQI indicate the higher index values; for the shallow samples, the ImpWQI indices are ranged from 178.69 to 1011 which indicate poor to extremely poor water quality. For the deep samples, the ImpWQI indicated that the samples with Na-Cl water type indicate the low water quality then the other water types.
The spatial distribution of the water quality based on the three indices (EWQI, WQI, and ImpWQI) is shown in Fig. 15.
For the both aquifers, the ImpWQI method shows the best result; it indicates that the Na-Cl water type coincides with the poor, and the extremely poor water quality and the two other indices (WQI and EWQI) indicate good to poor water types. These results reflect the effect of the parameter’s weight in the calculation of the water quality index.
Irrigation purposes
The collected samples were assessed for irrigation uses using different indices; the results are illustrated in the Table 7. According the TH (total hardness) values, all samples of the both aquifers present a soft water (TH < 75).
Table 7 Irrigation quality indices of Hajeb Layoun-Jelma aquifers The EC values of HJB are ranked into various categories for the both aquifers (shallow and deep aquifer). For the deep aquifer, 79% of samples present good to permissible water quality and 21% of samples indicated a doubtful water class (samples with Na-Cl water type). For the shallow aquifer, 21% of samples are permissible; 79% of samples present doubtful to unsuitable water class (including samples with Na-Cl water type). The %Na indicated that only 71% shallow samples are permissible for irrigation; the %Na of samples with Na-Cl water type varies from 54.3 to 76.71 indicating permissible to doubtful water quality. For the deep samples, three samples (F7, F9, and F10) present a good water class which coincide with the Ca-Cl and Ca-Mg-Cl water type; 58% (Na-Cl water type) indicate permissible water for irrigation, and three samples (Na-Cl water type; F2, F8, and F13) indicate a doubtful water class. The SAR values for HJB samples are ranked into two groups; for the both aquifers, all samples have a low degree of alkalinity hazards (2 < SAR < 10), except three samples with a high alkalinity hazards (10 < SAR < 18). Based only on the SAR values, the samples of HJB are distributed on two water classes (“excellent” to “good”) and its can be utilized for most types of soil. According the calculated values of MH (magnesium hazard) and the PI (permeability index), all samples of the shallow, springs, and deep aquifers are unsuitable for irrigation. The calculated values of Kr show that the groundwater samples of HJB, with Na-Cl water type, are more than 1, indicating moderate to unsuitable water quality for irrigation uses. Based on the seven estimated indices, the most of HJB’s samples are unsuitable for irrigation uses which the shallow samples present an irrigation quality less than the deep samples, and it is due to the shallow aquifer position, the thickness of the vadose zone which has a strong effect on the pollutants infiltration.
WILCOX and USSL classification
The %Na vs. EC values for HJB’s samples were plotted in the Wilcox graphical diagram of irrigation water (Wilcox 1955). The diagram shows that 10 samples present a water quality permissible to doubtful (Na-Cl water type), 3 samples are classed under good to permissible (Ca-Cl and Na-Cl water type), 13 samples are doubtful to unsuitable (Na-Cl water type), and 2 samples are excellent to good (Ca-Cl and Ca-Mg-Cl water type) (Fig. 16a).
The SAR vs. EC values for groundwater samples of HJB were plotted in the USSL diagram of irrigation water (Fig. 16b). Based on USSL diagram (USSL 1954), the water samples show five categories; “C2-S1” (medium salinity with low sodium), “C3-S1” (high salinity with low sodium), “C4-S2” (very high salinity with medium sodium), “C3-S2” (high salinity with medium sodium), and “C4-S3” (very high salinity with high sodium). Based on the combination between EC and SAR, in USSL diagram, HJB have only two deep samples suitable for irrigation (F9 and F10) (medium salinity with low sodium) which coincide with Ca-Cl and Ca-Mg-Cl water type.