Int J App Pharm, Vol 13, Issue 6, 2021, 221-231Original Article

HYDROCHEMICAL CHARACTERISTICS AND WATER QUALITY ASSESSMENT IN ABU-ZAABAL AREA, EASTERN NILE DELTA, EGYPT

RAGAA EL-SHEIKH1, IBRAHIM HEGAZY1, EHAB ZAGHLOOL2, MOHAMED E. A. ALI2, AYMAN A. GOUDA1*

1Chemistry Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt, 2Hydrogeochemistry Department, Desert Research Centre, Cairo, Egypt
Email: aymangouda77@gmail.com

Received: 17 Jun 2021, Revised and Accepted: 16 Aug 2021


ABSTRACT

Objective: The study presents simple tools for water resources quality classification based on its chemical compositions in Abu Zaabal area, eastern Nile Delta, Egypt and assess the water quality for different uses.

Methods: 31 water samples were collected from different water resources in the study area and analyzed for physicochemical parameters. Hydrochemical relations, contour maps and statistical methods were used to estimate the contamination indices and evaluate the water resources for different purposes.

Results: 83.3% of groundwater samples is fresh water and 16.7% are brackish water. 85.7% of surface water samples are fresh and 14.3% is saline. 92% of groundwater samples and 71.5% of surface water samples are very hard water. According to HPI values, 8% of the quaternary groundwater samples are good, 4% are poor, 4% are very poor and 84% of the samples are unsuitable. All groundwater samples and 71% of surface water samples are contaminated with respect to ammonia.

Conclusion: Higher concentrations of TDS and heavy metal may be due to the clay nature of the soil, the marine sediments in the aquifer matrix together with the dissolution and leaching of minerals from agricultural, anthropogenic and industrial activities. The groundwater in the polluted zones is considered unsuitable for human drinking.

Keywords: Water resources, Hydrochemistry, Water quality indices


INTRODUCTION

Surface and Groundwater have an associated hydrological relationship affected by different factors related to geological; hydrological and climatic conditions where these factors control the circumstances of groundwater movement in shallow aquifers as well as the quantity of water can be gained or lost from the aquifer and river [1].

Due to industrial and agricultural activities, large amounts of untreated urban, industrial wastewater and rural household waste discharge into the Nile River, canals or agricultural drain, which become an easy dumping site for all types of wastes [2]. Ismailia Canal is the most distal downstream of the principal Nile River. And the water contains all the toxins that are discharged into the Nile. The Ismailia Canal has many pollution sources which potentially affect and deteriorate the canal's water quality [3]. Heavy metals are considered to be a serious pollution of aquatic ecosystems due to their environmental persistence and toxicity effects on living organisms [4]. In the aquatic environment, trace elements are partitioned between different environmental components (water, suspended solids, sediments and biota [5]. Water resources chemistry is due to long-term interaction between the water systems and the surrounding environment, which can indicate the water formation and migration [6, 7].

The objective of this present study is to highlight the chemical compositions of different water resources in Abu Zaabal area, Eastern Nile Delta, Egypt. Assess the water quality for different uses.

The study area lies in the eastern portion of the River Nile delta in Qalyoubiya governorate, northeast Cairo city bounded by longitudes 31.320 and 31.440 E and latitudes 30.240 and 30.320 N, (fig. 1) occupies about 20 km2. The study area is bounded by Cairo ring road from the North, Belbis city from the south, Shebin El Qanater city from the west and Cairo–Belbeis desert road from the east.

Fig. 1: The location map and sampling points of the area under investigation

Abu Zaabal is considered as a plain area with an average elevation of 27 m above the mean sea level [8]. The area under investigation is characterized by cultivating lands surrounded by urban localities, The urban area is served by freshwater pipelines coming from a Mostorod water station is situated in the northern part of the study area as well as many shallow-private wells have been drilled for water extraction.

Geologically The Pleistocene and Holocene quaternary deposits cover most of the study area; the Basaltic rocks belonging to an Upper Oligocene age are exposed at Abu Zaabal area, while the Pliocene and Miocene sediments outcrops at the eastern part of Ismailia canal. The Holocene Nile silt and clay cover the majority of the study area with different thickness varies from 0 to 20 m, the sand dune unites belongs to the Holocene age found in the eastern part of the study area.

The hydrological conditions and the groundwater aquifers of the eastern portion of the Nile delta were discussed by many authors [9-13].

The surface water infrastructure in the study area consists of a network of the surface water system (Ismailia canal, Belbies drain and Shebin El Qanater drain). The surface water systems are passing through Holocene deposits (Nile silt and clay deposits) and the Pleistocene sediments after the disappearance of the Holocene deposits. The contaminated liquids are directly discharged into canals, drain and on the land surface. The Pleistocene aquifer is influenced by the contaminated water infiltrates due to the small thickness of the clay cap.

The Quaternary aquifers are discriminated into the upper unit (Holocene aquitard) and the lower one (the Pleistocene aquifer) [11, 13 and 14]. The Pleistocene aquifer is overlain by the Holocene unit and underlain by the Pliocene clay in the majority of the area. Around Abu Zaabal Quarries, it is underlain by Miocene sediments or the Oligocene Basaltic sheet. The Holocene aquifer is composed of the Nile silt and clay, with thickness ranges between 0 m at the eastern portions of 20 m at the southwestern part of the study area. The Pleistocene aquifer consists of sand and gravel with clay lenses with thickness ranges between 0 to nearly 50 m, while at the northwestern part of the investigated area, they may reach 200 m. The groundwater movements in the Pleistocene aquifer are mainly due north and northwest reflected that Ismailia canal is the main recharging source as the surface water level in the canal is higher than the groundwater level. Besides, the recharges from irrigation canals and return flow after irrigation. Septic tanks and sewer systems are considered a local source of recharge. The main discharge of the Pleistocene aquifer takes place artificially through pumping wells used for irrigation and domestic uses.

MATERIALS AND METHODS

Sampling procedures

Thirty-one water samples were collected from different water resources (24 samples from groundwater wells and 7 samples represents surface water systems) in August 2019; Surface water samples were collected using an autosampler and polyvinyl chloride Van Dorn bottle

Field measurements

The location (longitudes and latitudes) of the water points was recorded using global positioning system (GPS) model etrex 10 (Germany).

Water samples were collected in a 1000 ml clean polyethylene bottle which was used for major ions measurements, whereas a 50 ml clean polyethylene bottles was acidified with concentrated HNO3 to pH<2 for heavy metals detections. E. C and pH were measured in situ using portable meters (AD 310 and 3510, Jenway, UK).

Laboratory measurements

The chemistry of water samples was detected in Hydrogeochemistry laboratories, Desert Research Center, Cairo, Egypt. The measuring of the major, minor constituents of the water samples (total dissolved solids (TDS), major ions as Ca2+, Mg2+, Na+, K+, CO32-, HCO3-, SO42-, Cl-, NH4+, NO2-, NO3-and PO43-) were carried out according to the methods adopted by Bufflap SE and Allen HE (1995), Onken and Sunderman (1977), Fishman and Friedman (1985), Barer et al. (2000) and American Public Health Association (2005) [15-19] table 1.

Table 1: Methods adopted for water quality analysis

Quality parameter Method used
PH Potentiometric (1:2.5 H2O, v/v)
Electrical Conductivity EC Conductometery (1:2.5 H2O, v/v)
Calcium Ca2+ EDTA (0.05 N) titrimetric
Magnesium Mg2+ EDTA (0.05 N) titrimetric
Sodium Na+ Flame photometric
Potassium K+ Flame photometric
Chloride Cl- Titration using 0.05 N AgNO3
Carbonate CO32- Titration (with 0.01 N H2SO4)
Bicarbonate HCO3- Titration (with 0.01 N H2SO4)
Sulphate SO42- Spectrophotometric

After physiochemical analysis, the accuracy of the analysis results (% Balance error (%E)) was checked. Generally speaking, the relative error should be within±5%.

Heavy metals and trace components (Al, B, Cd, Co, Cr, Cu, Fe, Pb, Mn, Mo, Ni, Sr, V and Zn) were detected by plasma optical emission mass spectrometer (ICP) (POEMSIII, thermo Jarrell elemental company USA), using 1000 mg/l (Merck) Stock solution for standard preparation. The water quality parameters were estimated to evaluate the water resources in the study area (tables 2, 3).

RESULTS AND DISCUSSION

Physicochemical parameters of water resources

The physical and chemical analyses of water samples in Abu Zaabal area are summarized in (tables 4, 5).

Hydrogen ion concentration (pH)

The pH value reflects the acidic or alkaline material present in the water. The decrease of pH less than 7 reflects an increase in hydrogen ion concentration. Where the increase in pH more than 7 is reflects an increase in the hydroxyl ion. In the study area, the pH values range from 7.8 to 8.6 and from 8.0 to 8.7 for the ground and surface water, respectively, which indicates that the water resources in the study area are generally alkaline in nature.

Table 2: Water quality parameter estimation methods from measured parameters

Quality parameters Formula adopted Reference/source
Total dissolved solids (TDS) TDS = (Ca2++Mg2++Na++K++CO3-+(HCO3-/2)+SO42-+Cl-) [20]
Total hardness (TH) TH = (Ca+Mg) ˣ 50 [21]
Heavy metal pollution index (HPI)

HPI= (∑ Wi× Qi)/∑ Wi (1)

Wi is the unit weightage of the heavy metal (i), n is the number of heavy metals, Qi is the sub-index of the heavy metal.

Wi= (2) K is the proportionality constant; Si is the standard permissible limit of the heavy metal. K== (3)

Where, S1, S2, S3, and Si represent standards for different heavy metals in the groundwater samples. Qi= (4) Vi is the monitored value of the i parameter in mg/l, HPI is classified into five classes, excellent (0–25), good (26–50), poor (51–75), very poor (76–100) and unsuitable (100).

[22, 23]
Nitrate pollution index (NPI) Where Cs: The analytical concentration of nitrate. HAV: The threshold value of anthropogenic source (human affected value) taken as 20 mg/l. The water quality according to NPI values was classified into five types: clean (unpolluted)(NPI<0), light pollution (0<NPI<1), moderate pollution (1<NPI<2), significant pollution (2<NPI<3), very significant pollution (NPI>3). [24]
Drinking water quality index (DWQI)

The relative weight (Wi) is computed from the following equation: Wi = wi/ where Wi is the relative weight wi is the weight of each parameter n is the number of parameters qi= (Ci/Si) × 100 where qi is the quality rating Ci is the concentration of each chemical parameter in each water sample in milligrams per liter Si is the Egyptian drinking water standard for each chemical parameter in milligrams per liter according to the guidelines of the (Egyptian Higher Committee, 2007; WHO, 2011). For computing the WQI, the SI is first determined for each chemical parameter, which is then used to determine the WQI as per the following equation SIi =Wi × qi WQI =SIi where SIi is the sub-index of ith parameter qi is the rating based on the concentration of ith parameter n is the number of parameters

The standard is the standard of the water quality parameter. The water samples were classified according to WQI rate as excellent, good, poor, very poor and unfit for human consumption (table 4).

[25]
Sodium Adsorption Ratio (SAR) [26]
Residual Sodium Carbonate (RSC) RSC = (CO32-+HCO3-)-(Ca2++Mg2+) [27]
Sodium percentage (Na%) %Na = [(Na++K+)/(Na++K++Ca2++Mg2+)] X 100 [28]
Magnesium ratio (MAR) MAR = [Mg2+/(Ca2++Mg2+)] X 100 [29]
% Balance error (%E) %E = [(∑cation–anion)/(∑ cation+anion)] x 100 [20]

Table 3: Water quality parameters, their standard values, their ideal values and the assigned weighting factors

Parameter Standard value (Si) Weight (wi) Realative weight Wi
TDS 1000 5 0.161
Ca2+ 200 3 0.097
Mg2+ 150 3 0.097
Na+ 200 4 0.129
HCO3- 500* 1 0.032
SO42- 250 5 0.161
Cl- 250 5 0.161
NO3 45 5 0.161
The values according to Egyptian standards (2007) and WHO (2011) [30, 31]

Total dissolved solids (TDS)

The water salinity of groundwater ranges of 243 mg/l to 3390 mg/l and in surface water of 240 mg/l to 5600 mg/l, as shown in (fig. 2). 83.3% of groundwater samples are fresh water and 16.7% are brackish water. 85.7% from surface water samples are fresh and 14.3% is saline. Higher concentrations of may be credited to the impact of evaporation and the marine sediments in the aquifer matrix together with the dissolution and leaching of minerals from agricultural, anthropogenic and industrial activities [32, 33].

Total hardness

The total hardness (TH) is caused primarily by the presence of cations such as calcium and magnesium and anions such as carbonate, bicarbonate, chloride and sulfate in water. The total hardness values of groundwater samples range from 150 mg/l to 1300 mg/l reflected that 8% of these samples are hard and 92% are very hard water. The total hardness values in surface water range from 140 mg/l to 1480 mg/l reflected that 28.5% of samples are hard and 71.5% are very hard.

Fig. 2: TDS classification map for the quaternary groundwater in the study area

Soluble anions

Bicarbonate ion (HCO3-) source is from the dissolution of carbonate rocks (dolomite, limestone, magnesites etc.). HCO3 is mainly formed due to the action of CO2 from the atmosphere and that released from organic decomposition [34, 35]. Bicarbonate concentration in groundwater of the Quaternary (Pleistocene) aquifer varies from 138 mg/l to 520 mg/l and in surface water from 134 mg/l to 420 mg/l. The bicarbonate distribution in groundwater indicates that high content and the presence of local variations advocates the existence of local pollution sources. The distribution of bicarbonate salts increased from west to east. This direction may be due to the recharge of the quaternary aquifer from the Ismailia canal (fig. 3. a).

Sulfate ion (SO42-) is naturally formed due to rock weathering, input from volcanoes and biochemical process [36]. The oxidation and decomposition of substances containing sulfur (fossil fuels and dissolution of sulfur-bearing minerals such as gypsum and pyrite) and anthropogenic activities are other sources of SO4 ions [35]. The sulfate content in groundwater of the Quaternary aquifer varies from 23.1 mg/l to 780 mg/l and from 28.9 mg/l to 1080 mg/l in surface water. The groundwater distribution of sulfate indicates the presence of local zones of high concentrations at Abu Zaabal, reflecting that the effect of the saline pond from the west and the influence of the sulfate fertilizers in the new reclaimed land in the east (fig. 3. b).

The Cl-ion form in nature is usually of chlorine salts (CaCl2, MgCl2 and NaCl). The main source is due to the leaching and dissolution of sedimentary rocks; common evaporates minerals and saline deposits. Industrial, municipal wastes and irrigated agricultural activities are other main sources of chloride salts [37]. The chloride content varies from 32 mg/l to 970 mg/l in the quaternary groundwater samples and from 35 mg/l to 1750 mg/l in surface water. The chloride content distribution in groundwater shows the presence of local zones of high concentrations at Abu Zaabal. The local variations in the chloride concentrations are attributed to local recharge from the saline ponds in the study area; this also confirms the existence of local pollution sources (fig. 3. c).

Fig. 3: Spatial distribution map of anions concentrations in the quaternary groundwater in the study area

Soluble cations

Calcium plays an important role in the health of water bodies which reduces the toxicity of s chemical compounds in natural water [38]. The removal of Ca2+ ion from the water resources is due to an ion-exchange or calcite (CaCO32-) precipitation. Calcite precipitation occurs when CO2 content is low, causing the chemical reaction process in the reverse direction [35]. The calcium content in groundwater of the Quaternary aquifer varies from 32.8 mg/l to 392 mg/l and from 32.8 mg/l to 384 mg/l in the surface water samples. The calcium distribution in groundwater confirms the presence of local zones of high concentrations that occurred at Abu Zaabal (fig. 4. a). Hardness of water is attributed to the presence of calcium and magnesium ions; the water in the study area varied from hard to very hard.

A magnesium source water resources is due to chemical weathering and dissolution of dolomite, marls and other rocks [39]. Magnesium content in the Quaternary aquifer samples varies from 13.92 mg/l to 114 mg/l and from 11.5 mg/l to 124.8 mg/l in surface water. The magnesium distribution in groundwater shows the presence of local zones of high concentrations, but the magnesium contents are still below the excessive limits for drinking (fig. 4. b).

A sodium source in the water resources is due to weathering of Na bearing minerals/rocks (halite, feldspar and montmorillonite), cation-exchange process (displacement from absorbing complex of rocks and soils by Ca and Mg), and anthropogenic activities (pollution from industrial effluent, domestic sewage, and agricultural activities). Sodium content in groundwater of the Quaternary (Pleistocene) aquifer varies from 18 mg/l to 442.9 mg/l and from 20 mg/l to 1265 mg/l in surface water. The distribution of sodium ions in the study area reflects local variations may be attributed to local recharge from the saline ponds in the study area. The groundwater in the polluted zones is considered unsuitable for drinking (fig. 4. c). Potassium is slightly less common than sodium in igneous rocks, but more abundant in all sedimentary rocks. In igneous rocks, potassium is present as feldspars (orthoclase and microcline (KAlSi3O3)), wherein sediments it is present in clay minerals. Potassium is slightly less common than sodium in igneous rocks, but more abundant in all sedimentary rocks. In igneous rocks, potassium is present as feldspres (orthoclase and microcline (KAlSi3O3)), wherein sediments it is present in clay minerals. The concentration of potassium in natural water is generally less than 10 mg/l as much as 100 mg/l in hot springs and about 25000 mg/l in brines.

Minor, trace and heavy metals

Nitrate concentrations in the groundwater samples ranges between 12 mg/l to 42 mg/l and from 8 mg/l to 75 mg/l in the surface water samples. Nitrite concentration in the groundwater samples ranged between 0.05 mg/l to 0.51 mg/l and from 0.01 mg/l to 0.61 mg/l in the surface water samples. Ammonia concentration in the groundwater samples ranges between 0.5 mg/l to 3.7 mg/l and from 0.1 mg/l to 8 mg/l in the surface water samples. From the previous data, the groundwater samples are contaminated with ammonia. This shows that groundwater samples is mixed with sewage and the presence of Escherichia coli bacteria from bacteriological analysis of some groundwater samples proved that.

Iron content, 83.3% of groundwater samples in the Pleistocene aquifers of Abu Zaabal area are unsuitable for human drinking, while the rest of the samples (16.7%) are suitable for drinking. On the other hand, 71.4% of surface water samples are unsuitable for human drinking, while the rest of the samples (28.6%) are suitable for drinking. Iron values of groundwater ranges from 0.004 mg/l to 5.39 mg/l and in surface water from 0.03 mg/l to 6.96 mg/l. This is due to the clay nature of the soil.

Manganese content (33.3%) of the groundwater samples and 28.6% of surface water samples are unsuitable for drinking. Lead content (12.5%) of the groundwater samples is unsuitable for drinking. Cadmium content, (83.3%) of the groundwater samples and 71.4% of surface water samples are unsuitable for drinking. Aluminum content (8.3%) of the groundwater samples and 71.4% of surface water samples are unsuitable for drinking. Nickel content (12.5%) of the groundwater samples and 42.8% of surface water samples are unsuitable for drinking.

Fig. 4: Spatial distribution map of cations concentrations in the quaternary groundwater in the study area

Table 4: Major and minor element concentrations of water samples in Abu Zaabal area

 Sample pH EC TDS

T.

Hardness

Ca 2+ Mg 2+ Na+ CO3 2- HCO3- SO4 2- Cl- %E NH4+ NO2 NO3 PO4---
(μS/cm) (mg/l) (mg/l) (mg/l) (mg/l (mg/l) (mg/l) (mg/l) (mg/l) (mg/l) (mg/l) (mg/l) (mg/l)
  Surface water
1S 8 1375 880 355 82 36 130 8 220 170.2 225 -3.0 8 0.61 75 5.5
3S 8.1 375 240 140 36.8 11.5 20 2 136 29.3 37 -3.0 0.1 0.01 10 0
8S 8.1 8750 5600 1480 384 124.8 1265 10 420 1080 1750 3.5 5.5 0.6 70 18
9S 8.2 1390.6 890 360 88 33.6 125 9 223 171.1 218.7 -3.1 6.3 0.61 58 24
13S 8.7 806.3 516 239 62 20.2 76.7 2 134 108 156 -4.5 0.9 0.12 28 7.4
17S 8.5 406.3 260 196 52 15.8 21.5 4 140 32.9 58 2.3 0.9 0.14 14 3.8
29S 8.1 400 256 156 32.8 17.8 21.7 2 146 28.9 35 0.7 0.1 0.01 8 0.01
Groundwater
2G 8.5 392.2 251 161 32.85 18.9 18.2 4 138 32.3 32 2.0 0.9 0.05 16 2.7
4G 8.3 695.3 445 290 61.6 32.6 35 4 172 110.1 53 4.9 0.8 0.24 14 0.01
5G 7.8 4312.5 2760 1300 392 76.8 442.9 6 396 820 680 2.7 3.7 0.51 42 0.08
6G 7.8 1073.4 687 400 104 33.6 64 4 258 183.8 65 4.1 0.9 0.13 24 0.18
7G 7.9 1995.3 1277 643 144 68 170 4 316 392.4 187.8 3.9 1.1 0.15 25 0.27
10G 7.7 3031.3 1940 1075 240 114 225 4 440 547.1 395.8 2.3 1.5 0.19 26 0.01
11G 8.3 1378.1 882 525 164.8 27.1 95 8 318 217.5 131 4.1 1.4 0.17 25 0.05
12G 8 1315.6 842 436 96 47 115 6 234 158 200 3.4 0.7 0.08 19 0.01
14G 8 1226.6 785 346 96 25.7 115 2 240 98.3 238 -3.2 0.9 0.15 24 0.07
15G 7.7 5296.9 3390 780 172 84 860 8 520 780 970 0.7 2.3 0.51 30 0.03
16G 8.3 2625 1680 383 112 24.8 420 7 312 592.8 312 -0.7 1.1 0.16 19 0.27
18G 8.3 875 560 240 53.6 25.4 83.3 6 150 134.8 123 -2.0 1.8 0.22 28 0.26
19G 8.2 1953.1 1250 394 99.2 35 260 6 480 340.8 174 -1.9 1.2 0.15 24 0.37
20G 8.4 1054.7 675 336 76.8 34.6 116 4 292 140.8 120 2.7 1 0.13 18 0.05
21G 8.6 412.5 264 152 37.6 13.9 25 4 138 42 38.7 -1.4 1.6 0.09 27 0.01
22G 7.9 2229.7 1427 662.5 194 42.6 190 4 322 620.9 156 -2.6 1.1 0.16 23 0.01
23G 8 1129.7 723 422.5 130 23.4 80 4 298 140.6 136 1.0 0.9 0.09 18 0.028
24G 8.2 379.7 243 150 32.8 16.3 24.6 2 144 22.5 52.4 -3.1 0.6 0.08 16 0.01
25G 7.9 812.5 520 294 78.8 23.3 46.7 8 249 86.3 65.7 0.9 1.3 0.16 25 0.05
26G 7.8 721.9 462 366 102.4 26.4 35 4 280 69.2 72.9 4.2 0.5 0.07 12 0.01
27G 7.8 837.5 536 313 72 32 50 4 158 170.7 76 0.7 1.2 0.13 25 0.05
28G 8.1 1937.5 1240 760 258.4 27.4 110 4 162 620.6 117 2.7 2.5 0.17 26 0.01
30G 8.2 864.1 553 346.6 92 28 40 4 318 34.8 68 4.7 0.8 0.21 21 0.01
31G 8.1 760.9 487 356 72.8 41.8 42.9 8 296 23.1 103 4.0 2.5 0.15 32 0.01

Table 5: Trace and heavy metal concentrations of water samples in Abu Zaabal area in mg/l unit

 Sample Al Co Cu Cd Fe Pb Sr Mn Mo Ni Ba
Surface water
1S 1.29 0.035 0.050 0.042 2.368 <0.008 1.556 0.192 0.090 0.082 0.092
3S 1.26 0.097 <0.006 <0.0006 0.030 <0.008 0.400 0.090 0.107 <0.002 0.071
8S 14.29 <0.001 0.065 0.047 6.960 <0.008 12.290 0.819 0.036 <0.002 0.097
9S 1.04 <0.001 0.078 0.027 2.836 <0.008 1.578 0.158 <0.001 0.072 0.098
13S 2.01 0.007 0.039 0.028 1.430 <0.008 0.584 0.118 <0.001 <0.002 0.067
17S 0.01 <0.001 <0.006 0.015 1.827 <0.008 1.444 0.661 0.075 0.028 0.041
29S 0.15 0.010 0.034 <0.0006 0.061 <0.008 0.599 <0.002 0.025 <0.002 0.082
Groundwater
2G 0.10 0.023 <0.006 0.028 0.695 <0.008 0.348 0.035 0.043 <0.002 0.0720
4G <0.01 <0.001 <0.006 0.029 0.495 <0.008 0.645 0.192 0.027 <0.002 0.070
5G 0.08 0.008 0.006 0.050 0.463 <0.008 3.808 0.902 0.051 0.020 0.070
6G 0.16 0.010 0.022 0.026 0.518 0.052 1.909 0.421 0.003 0.011 0.069
7G 0.12 <0.001 0.012 0.009 0.445 <0.008 2.954 0.016 0.065 <0.002 0.060
10G 0.06 0.003 0.020 0.027 4.730 0.019 2.282 0.848 <0.001 0.028 0.135
11G 0.00 0.000 <0.006 0.024 3.980 <0.008 1.281 0.509 0.018 0.014 0.131
12G 0.11 <0.001 <0.006 0.025 0.500 <0.008 1.433 0.200 <0.001 0.010 0.111
14G 0.0738 0.033 0.021 0.009 0.304 <0.008 0.857 0.206 0.112 <0.002 0.030
15G <0.01 0.039 <0.006 0.045 0.159 0.156 4.524 0.843 0.064 0.035 0.0469
16G 0.03 0.043 0.019 0.003 5.390 <0.008 4.795 0.921 0.051 <0.002 0.049
18G 0.33 0.072 <0.006 <0.0006 2.220 <0.008 0.332 0.041 <0.001 <0.002 0.034
19G <0.01 0.021 0.014 0.011 2.190 <0.008 1.394 0.115 0.003 0.013 0.138
20G 0.16 <0.001 0.001 0.018 0.940 <0.008 0.463 0.044 0.061 <0.002 0.067
21G 0.05 0.001 0.057 0.056 0.218 <0.008 7.011 0.221 <0.001 <0.002 0.144
22G <0.01 <0.001 <0.006 0.038 1.277 <0.008 1.564 0.139 0.000 <0.002 0.497
23G 0.04 0.062 <0.006 0.025 0.777 <0.008 0.337 0.102 <0.001 <0.002 0.073
24G <0.01 0.049 0.024 0.011 0.028 <0.008 1.315 0.008 <0.001 <0.002 0.089
25G <0.01 0.021 0.032 0.037 0.004 <0.008 0.728 0.088 <0.001 0.015 0.143
26G 0.18 0.047 0.085 0.071 0.400 <0.008 1.112 0.881 0.159 <0.002 0.307
27G <0.01 <0.001 0.001 <0.0006 2.670 <0.008 4.574 0.061 0.067 0.054 0.083
28G 1.20 0.019 0.034 0.070 2.259 <0.008 0.339 0.108 0.171 0.010 0.041
30G 0.07 <0.001 <0.006 <0.0006 1.151 <0.008 1.243 0.189 <0.001 0.015 0.080
31G 0.18 0.008 0.004 0.023 0.436 <0.008 0.400 0.726 0.040 <0.002 0.078

Water resources contamination indices

Nitrate pollution index

The source of nitrate in the groundwater is classified to nonpoint sources such as intensive agricultural activities and point sources such as irrigation of land by sewage effluents [40]. The surface water samples in the Abu Zaabal area are classified according to NPI values as follows: 43 % of the samples are cleaned (unpolluted), 14% are light-polluted, 14% of the samples are moderately polluted and 28% are significant pollution. Where the groundwater samples are 33% of samples are clean (unpolluted), 63% are samples are light polluted and 4% of the samples are moderate polluted table 6. The distribution of the NPI values presented that the majority of the study area located under light-polluted zone may be due to the influence of agricultural activities (nitrification of synthetic fertilizers and soil organic nitrogen). Where is the moderate pollution is located close to Bilbeis drain reflected the influence of groundwater recharge from the drain (fig. 5).

Heavy metal pollution index (HPI)

The Heavy metal pollution index (HPI) for water resources in the study area was calculated based on the concentration of Al, Cu, Cd, Fe, Pb, Mn, Mo and Ni use the permissible limits according to WHO, 2011. HPI of surface water samples ranged between 31.8 and 993.2 reflected wide variation in the surface water resources in the study area (table 6). Ismailia canal samples (3S and 29 S) are classified as good samples according to HPI values. The Quaternary groundwater samples can be classified according to HPI values as: 8% of the quaternary groundwater samples are good, 4% are poor, 4% are very poor and 84% of the samples are unsuitable. The distribution map of HPI values (fig. 6) reflects the increasing of the HPI values in the majority of the study area may be due to wider sources of pollution.

Fig. 5: Spatial distribution of the NPI values for the quaternary water samples in Abu Zaabal area

Fig. 6: Spatial distribution of the HPI values for the quaternary water samples in Abu Zaabal area

Table 6: The contamination indices, water quality indices for drinking and evaluation for water resources in the study area

Sample NPI HPI DWQI SAR % Na MR RSC
Surface water samples
1S 2.75 993.2 82.6 3 58.5 72.4 -3.2
3S -0.5 40.7 16.4 0.7 35.8 51.6 -0.5
8S 2.5 1136.2 408.4 14.3 78.4 53.6 -22.2
9S 1.9 655.3 76.1 2.9 62.9 62.9 -3.2
13S 0.4 644.3 45.4 2.2 57.9 53.6 -2.5
17S -0.3 366.6 20.9 0.7 35.4 50.2 -1.5
29S -0.6 31.8 16.2 0.8 35.7 89.2 -0.6
Groundwater samples
2G -0.2 634.9 18.8 0.6 33.2 95.1 -0.8
4G -0.3 655.5 31.1 0.9 32.9 87.3 -2.8
5G 1.1 1127.2 211.1 5.4 59 32.3 -19.2
6G 0.2 681.1 48.7 1.4 41.3 53.2 -3.6
7G 0.25 218.4 91.2 2.9 53.8 77.8 -7.5
10G 0.3 655.5 137.6 3 46.7 78.3 -14
11G 0.25 559.3 63.5 1.8 44.6 27.1 -5
12G -0.05 571.1 60.0 2.4 52.8 80.8 -4.6
14G 0.2 220 58.2 2.7 59.2 44.1 -2.9
15G 0.5 1316.6 250.6 13.4 81.6 80.5 -6.7
16G -0.05 97.8 128.2 9.4 81.2 36.5 -2.3
18G 0.4 36.5 46.2 2.3 59.6 78.2 -2.1
19G 0.2 268.7 88.8 5.7 74.2 58.2 0.2
20G -0.1 417.1 49.4 2.8 60.6 74.2 -1.8
21G 0.35 1246.4 24.3 0.9 42 61 -0.6
22G 0.15 853.5 107.7 3.2 54.3 36.2 -7.8
23G -0.1 567.3 50.8 1.7 43.9 29.7 -3.4
24G -0.2 258.3 19.6 0.9 39.8 82 -0.6
25G 0.25 835.2 37.0 1.2 39.6 48.7 -1.5
26G -0.4 1583.7 31.6 0.8 27.9 42.5 -2.6
27G 0.25 64.3 43.3 1.2 40.2 73.2 -3.5
28G 0.3 1574.4 99.2 1.7 37.2 17.5 -12.4
30G 0.05 39.5 33.9 0.9 31.3 50.2 -1.5
31G 0.6 525.7 38.3 1 29.6 94.5 -1.9

Evaluation of groundwater for human drinking

The comparison between the maximum permissible limits major, minor, trace and heavy metals for human drinking (table 7) with the concentrations of these constituents in groundwater and surface water of the investigated samples in the study area leads to the following conclusions:

  1. Evaluation of water in human drinking suitability according to physical properties reflected that 100% of water samples (ground and surface) are suitable in respect to pH. 66.7% of groundwater samples and 85.7% of surface water samples are suitable for human drinking in respect to TDS. 70.8% of groundwater samples and 85.7% of surface water samples are suitable for human drinking in respect to TH.

  2. Evaluation of water for human drinking suitability according to major constituents reflected that 100%, 91.6%, 66.7%, 83.3% and 79.2% of groundwater samples are suitable for drinking purposes in respect to Mg, Ca, SO4, Cl and Na, respectively. 100% and 85.7% of surface water samples are suitable for drinking purposes in respect (Mg, Ca) and (SO4, Cl, Na), respectively.

  3. Evaluation of water for human drinking suitability according to minor–trace constituents and heavy metals reflected that:

Table 7: Water quality guidelines used in evaluation for human drinking water quality index

Parameter Egyptian1 maximum permissible limit in mg/l (2007) [30] WHO guidelines for human drinking 2003 [41]
pH-value 6.5–8.5 6.5-9.5
Na (mg/l) 200 200
Mg (mg/l) 150 150
K (mg/l) 12
Ca (mg/l) 350 200
Cl (mg/l) 250 250
SO4 (mg/l) 250 250
NO3 (mg/l) 45 50
TDS (mg/l) 1000 (at 120 C) 1000
Hardness as CaCO3 (mg/l) 500 500
Al (mg/l) 0.2 0.2
Fe (mg/l) 0.3 0.3
Mn (mg/l) 0.4 0.4
Cu (mg/l) 2 2
Zn (mg/l) 3 3
Pb (mg/l) 0.01 0.01
Cr (mg/l) - 0.05
Cd (mg/l) 0.005 0.003
Ni (mg/l) 0.02 0.02
B (mg/l) 0.5 0.5

Fig. 7: Spatial distribution of the DWQI values for the quaternary water samples in Abu zaabal area

Table 8: Water quality index scale

Range Type of water
<50 Excellent
50–100 Good water
100.1-200 Poor water
200.1-300 Very poor water
>300 Water unsuitable for drinking purposes

The evaluation of water resources for irrigation purposes

The suitability of water for irrigation is determined by its mineral constituents and the type of the plant and soil to be irrigated. Water quality used for irrigation is well recognized as an important factor in the productivity of crops. The suitability of water for irrigation is determined not only by the total amount of salt present but also by the kind of salt. Different chemical factors affecting the suitability of water for irrigation and its effect on crop production and soil quality. Among these are:

-Salinity hazard (EC)-total soluble salt content

-Sodium hazard (SAR)

-Sodium percentage (Na %):

-Magnesium ratio (MR)

-Residual sodium carbonate (RSC)

Salinity hazard (EC)

Based on the EC, irrigation water can be classified into four categories [42] as shown in table 9.

Table 9: Classification of irrigation water based on salinity (EC) values

Level EC (µS/cm) Total dissolved salts (mg/l) Hazard and limitations
C1 <250 <200 Low hazard; no detrimental effects on plants, and no soil buildup expected.
C2 250-750 200-500 Sensitive plants may show stress; moderate leaching prevents salt accumulation in soil.
C3 750-2250 500-1500 Salinity will adversely affect most plants; requires selection of salt-tolerant plants, careful irrigation, good drainage, and leaching.
C4 >2250 >1500 Generally unacceptable for irrigation, except for very salt tolerant plants, excellent drainage, frequent leaching, and intensive management.

Based on this classification, it should be noted that 20.8% of groundwater samples (samples Nos. 2 G, 4G, 21G, 24G and 26G) and 42.85% of surface water samples (samples Nos. 3S, 17S, and 29S) are classified as class C2. 62.5% of groundwater samples (Samples Nos. 6G, 7G, 11G, 12G, 14G, 18G, 19G, 20G, 22G, 23G, 25G, 27G, 28G, 30G and 31G) and 42.85% of surface water samples (Samples Nos. 1S, 9S and 13S,) are classified as class C3 which are saline and then require selection of salt-tolerant plants, careful irrigation, good drainage, and leaching. 16.7% of groundwater samples (samples Nos. 5G, 10G, 15G and 16G) and 14.3% of surface water samples (Sample No. 8S) are classified as class C4.

Sodium adsorption ratio (SAR)

Continued use of water having a high SAR leads to a breakdown in the physical structure of the soil. The sodium replaces calcium and magnesium sorbed on clay minerals and causes dispersion of soil particles. This dispersion results in the breakdown of soil aggregates and causes cementation of the soil under drying conditions as well as preventing infiltration of rainwater. Classification of irrigation water based on SAR values is shown in table 10.

Based on this classification, it should be noted that all samples are classified as class S1 except samples 8S and 15G are classified S2 table 6. 20.8% of groundwater samples (samples Nos.2G, 4G, 21G, 24G and 26G) and 42.85% of surface water samples (samples Nos. 3S, 17S, and 29S) in the study area lie in the fields C2-S1. 62.5% of groundwater samples (Samples Nos. 6G, 7G, 11G, 12G, 14G, 18G, 19G, 20G, 22G, 23G, 25G, 27G, 28G, 30G and 31G) and 42.85% of surface water samples(Samples Nos. 1S, 9S and 13S,) lie in the fields C3-S1.16.7% of groundwater samples (samples Nos. 5G, 10G and 16G) lie in the fields C4-S1. 4.2% of groundwater samples (samples No. 15G) and 14.3% of surface water samples (Samples No. 8S) lie in the fields C4-S2, which reflect unacceptable for irrigation, except for very salt-tolerant plants, excellent drainage, frequent leaching, and intensive management and problems on fine texture soils and sodium-sensitive plants, especially under low-leaching conditions, but could be used on sandy soils with good permeability.

Sodium percentage (Na %)

The groundwater samples are suitable for irrigation in 33.3% of samples and 42.8% of surface water samples according to Na% values. 50% and 28.6% from groundwater samples and surface water samples, respectively, were Permissible. 8.3% and 28.6% from groundwater samples and surface water samples, respectively, were doubtful. 8.3% and zero% from groundwater samples and surface water samples, respectively, were unsuitable (table 11).

Table 10: Classification of irrigation water based on SAR values [42]

Level SAR Quality Hazard
S1 <10 Low sodium No harmful effects from sodium.
S2 10-18 Medium sodium Problems on fine texture soils and sodium-sensitive plants, especially under low-leaching conditions, but could be used on sandy soils with good permeability.
S3 18-26 High sodium Harmful effects could be anticipated in most soils and amendments such as gypsum would be necessary to exchange sodium ions.
S4 >26 Very high sodium Generally unsatisfactory for irrigation.

Table 11: Suitability for irrigation based on sodium percent

Na% Suitability for irrigation No. of samples Percentage (%)
<20 Excellent - -
20-40 Good 8 G-3S 33.33-42.8
40-60 Permissible 12G-2S 50-28.6
60-80 Doubtful 2G-2S 8.33-28.6
>80 Unsuitable 2G 8.33

Magnesium ratio (MR)

Calcium and magnesium maintain equilibrium in most waters, in equilibrium. Mg2+in the waters will adversely affect crop yield; magnesium impact on irrigated water is expressed as magnesium ratio (MR) (MR>50% is suitable for irrigation and MR<50% is unsuitable).

M. R values reflected that 45.8% of investigating groundwater samples are unsuitable for irrigation table 6.

Residual sodium carbonate (RSC)

An excess of sodium bicarbonate and carbonate is considered to be detrimental to the physical properties of soils as it causes dissolution of organic matter in the soil, which in turn leaves a black stain on the soil surface on drying; this excess amount is denoted by Residual Sodium Carbonate (RSC).

All samples (ground and surface) is good for irrigation table 6. (R. S. C>2.5 meq/l is unsuitable for irrigation, RSC values from 1.25 to 2.5 meq/l are doubtful and R. S. C<1.25 meq/l are good for irrigation) [43].

CONCLUSION

The water resources in the study area are generally alkaline in nature. 83.3% of groundwater samples are fresh water and 16.7% are brackish water. 85.7% of surface water samples are fresh and 14.3% is saline. The groundwater distribution of sulfate indicates the presence of local zones of high concentrations at Abu Zaabal, reflecting the effect of the saline pond from the west and the influence of the sulfate fertilizers in the new reclaimed land in the east. The NPI values presented that the majority of the study area located under light polluted zone due to the influence of agricultural activities (nitrification of synthetic fertilizers and soil organic nitrogen) and moderate pollution zone is located closed to Bilbeis drain reflected that the influence of groundwater recharge from the drain According to WQI values, the distribution of drinking water quality index values for the groundwater samples in Abu Zaabal area reflected the effect of the Belbis drain on the groundwater quality. 33.3% of groundwater and 42.8% of surface water samples are suitable for irrigation according to Na% values. 45.8% of investigated groundwater samples are unsuitable for irrigation according to M. R values.

FUNDING

Nil

AUTHORS CONTRIBUTIONS

Prof. Dr. Ragaa El-Sheikh; Prof. Dr. Ayman A. Gouda and Dr. Ehab Zaghlool have been generated the research idea and interpreted the data and helped to draft the manuscript. Dr. Mohamed E. A. Ali has suggested the research idea and participated in the design of the study. Mr. Ibrahim Hegazy was prepared the solutions, carried out the experiments, interpreted the data and helped to draft the manuscript.

CONFLICTS OF INTERESTS

The authors confirm that this article's content has no conflict of interest.

REFERENCES

  1. Al-Shamaa IM, Ali BM. Hyrological relationship between surface and groundwater in badra-jassan basin. Iraqi J Sci. 2012;2:335-40.

  2. Drain B, El-Baqar Drain B. System/Egypt environmental studies on water. Quality; 2009.

  3. Geriesh MH, Balke KD, El-Rayes AE. Problems of drinking water treatment along Ismailia Canal Province, Egypt. J Zhejiang Univ Sci B. 2008;9(3):232-42. doi: 10.1631/jzus.B0710634, PMID 18357626.

  4. Khalil MK, Radwan A, El-Moselhy KM. Distribution of phosphorus fractions and some of the heavy metals in surface sediments of Burullus lagoon and the adjacent Mediterranean Sea. Egypt J Aquat Res. 2007;33:277-89.

  5. Abbas M, Shakweer L. Effect of ecological and biological factors on the uptake and concentration of trace elements by aquatic organisms at Edku Lake. Egypt J Aquat Res. 2005;31:271-87.

  6. Gupta NV, Hm N, G R. Validation of the water purification system. Asian J Pharm Clin Res. 2017;10(4):409-16. doi: 10.22159/ajpcr.2017.v10i4.16955.

  7. Rashid I, Romshoo SA. Impact of anthropogenic activities on water quality of Lidder River in Kashmir Himalayas. Environ Monit Assess. 2013;185(6):4705-19. doi: 10.1007/s10661-012-2898-0, PMID 23001554.

  8. Korany E, Abdel Aal M. Groundwater response in the urban sectors of Cairo environs, Egypt. In: Hydrological processes and water management in urban areas. International Symposium; 1988. p. 429-36.

  9. El-Fakharany MA, Mansour NM, Yehia MM, Monem M. Evaluation of groundwater quality of the Quaternary aquifer through multivariate statistical techniques at the southeastern part of the Nile Delta, Egypt. Sustain Water Resour Manag. 2017;3(1):71-81. doi: 10.1007/s40899-017-0087-6.

  10. Korany B, Brynen R, Noble P. The analysis of national security in the Arab context: restating state of the art. In: The many faces of national security in the Arab world Palgrave. London: Macmillan; 1993. p. 1-23.

  11. Taha AA, Serag El-Din H, El-Hadad M. Hydrogeological situation of the area between ismailia canal and caro–ismailia desert road. J Environ Sci. 1997;14:147-79.

  12. Pawlikowski M, Pająk L, Mazurek J, Eweida A, Mahmoud K. Wody geotermalne Zatoki Suezkiej (Egipt) i możliwości ich praktycznego wykorzystania. Gospod Surowcami Min. 1999;15:89-97.

  13. Yehia MM. Environmental impacts of sewage irrigation water on groundwater quality of northeast Cairo, Egypt. Eur Res J. 2000;72:176-93.

  14. El Fakharany MA, Mansour NM. Assessment of water resources quality at the southeastern part of the Nile Delta, Egypt. ICWCAR; 2009. p. 12-4.

  15. Onken A, Sunderman HD. Colorimetric determinations of exchangeable ammonium, urea, nitrate, and nitrite in a single soil extract1,2. Agron J 1977;69(1):49-53. doi: 10.2134/agronj1977.00021962006900010013x.

  16. Fishman MJ, Friedman LC, Chapter A. Methods for determination of inorganic substances in water and fluvial sediments. US Geol Surv. In: Open-file report, Denver, CO, USA. Bk. 5; 1985. p. 485-98.

  17. Brar MS, Malhi SS, Singh AP, Arora CL, Gill KS. Sewage water irrigation effects on some potentially toxic trace elements in soil and potato plants in northwestern India. Can J Soil Sci. 2000;80(3):465-71. doi: 10.4141/S99-106.

  18. APHA (American Public Health Association). Standard methods for the examination of water and wastewater. 21st ed. Washington, DC: American Public Health Association; 2005.

  19. Appelo A, Postma D. Geochemistry, groundwater and pollution. 2nd ed. Balkama, Rotterdam; 2005.

  20. Ragunath HM. Groundwater. New Delhi: Wiley Eastern Ltd; 1987. p. 563-69.

  21. Horton RK. An index number system for rating water quality. J (Water Pollut Control Fed). 1965;37:300-6.

  22. Mohan S, Nithila P, Reddy S. Estimation of heavy metal in drinking water and development of heavy metal pollution index. J Environ Sci Health. 1996;31:283-9.

  23. Spalding RF, Exner ME. Occurrence of nitrate in groundwater- a review. J Environ Qual. 1993;22(3):392-402. doi: 10.2134/jeq1993.00472425002200030002x.

  24. Kumar GVSRP, Sanand VS, Kumar NS, Murthy BS. Assessment of water quality of Thatipudi reservoir of vizianagaram distrinct of Andhra Pradesh. Innovare J Sci. 2013;1:20-4.

  25. Doneen LD. Notes on water quality in agriculture. Water science and engineering. Department of Water Sciences and Engineering, University of California; 1964. p. 4001.

  26. Ayers RS, Westcot DW. Water quality for agriculture. Rome: food and agriculture organization of United Nations; 1985. p. 174.

  27. Khodapanah L, Sulaiman WNA, Khodapanah N. Groundwater quality assessment for different purposes in Eshteharddistrict, Tehran, Iran. Eur J Sci Res. 2009;36:543-53.

  28. Paliwal KV. Irrigation with saline water. ICARI Monograph No. 2 (New Series). New Delhi; 1972. p. 198.

  29. Egyptian Higher Committee for Water. Water quality guidelines for human drinking, domestic and laundry uses. Egypt; 2007.

  30. World Health Organization (WHO). Guidelines for drinking water quality, 4thed. Geneva; 2011. p. 924-78.

  31. El-Sayed MH, El-Aassar AM, El-Fadl MA, El-Gawad AM. Hydro-geochemistry and pollution problems in 10th of Ramadan City, East El-Delta, Egypt. JASR. 2012;4:1959-72.

  32. Taha A, El-Mahmoudi A, El-Haddad I. Pollution sources and related environmental impacts in the new communities southeast Nile Delta, Egypt. EJER. 2004;9:35-49.

  33. Goher ME, Hassan AM, Abdel-Moniem IA, Fahmy AH, El-sayed SM. Evaluation of surface water quality and heavy metal indices of Ismailia Canal, Nile River, Egypt. Egypt J Aquat Res. 2014;40(3):225-33. doi: 10.1016/j.ejar.2014.09.001.

  34. Nikanorov AM, Brazhnikova LV. Types and properties of water II: Water chemical composition of rivers. Lakes Wetlands. 2009;2:42-80.

  35. Islam MJ, Hossain AM, Rahman MS, Khandoker MH, Zahan MN. Hydrogeochemistry and usability of groundwater at the Tista river basin in Northern Bangladesh. IJST. 2019;12(47):1-12. doi: 10.17485/ijst/2019/v12i47/147961.

  36. El-Rawy M, Ismail E, Abdalla O. Assessment of groundwater quality using GIS, hydrogeochemistry, and statistical factor analysis in Qena governorate, Egypt. Desalin Water Treat. 2019;162:14-29. doi: 10.5004/dwt.2019.24423.

  37. Lewis WM, Morris DP. Toxicity of Nitrite to Fish: A Review. Trans Am Fish Soc. 1986;115(2):183-95. doi: 10.1577/1548-8659(1986)115<183:TONTF>2.0.CO;2.

  38. Ramesh K, Jagadeeswari BP. Hydrochemical characteristics of groundwater for domestic and irrigation purposes in Periyakulam taluk of Theni district, Tamil nadu. Int Res J Environ Sci. 2012;1:19-27.

  39. McLay CDA, Dragten R, Sparling G, Selvarajah N. Predicting groundwater nitrate concentrations in a region of mixed agricultural land use: a comparison of three approaches. Environ Pollut. 2001;115(2):191-204. doi: 10.1016/s0269-7491(01)00111-7, PMID 11706792.

  40. World Health Organization (WHO). WHO guidelines for drinking-water Quality. Chromium in Drinking-Water; 2003.

  41. College of Agriculture sciences. Irrigation water quality. Pennsylvania State Univ. Ersity USA; 2002.

  42. El Behairy RA, El Baroudy AA, Ibrahim MM, Shokr MS. Assessment and mapping of surface water quality index for irrigation purpose: case study northwest of Nile Delta, Egypt. Menoufia J Soil Sci. 2021;6(5):163-82. doi: 10.21608/ mjss.2021.182346.