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Hydrochemical and quality of water resources in Saudi Arabia ...

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44<br />

Proceed<strong>in</strong>gs <strong>of</strong> the International Academy <strong>of</strong> Ecology <strong>and</strong> Environmental Sciences, 2013, 3(1): 42-51<br />

Fig. 1 Location <strong>of</strong> studied areas<br />

2.2 Water <strong>quality</strong> measurements<br />

The <strong>water</strong> pH, EC, soluble ions, Boron, <strong>and</strong> Heavy metals were determ<strong>in</strong>ed as follow:<br />

i: The Water reaction (pH) was determ<strong>in</strong>ed us<strong>in</strong>g a pH meter (pH meter - CG 817).<br />

ii: The Total soluble salts was measured by us<strong>in</strong>g electrical conductivity meter (EC) <strong>in</strong> dS/m at 25 o C (Test kit<br />

Model 1500_20 Cole <strong>and</strong> Parmer).<br />

iii: The Soluble Potassium <strong>and</strong> Sodium were determ<strong>in</strong>ed by us<strong>in</strong>g flame photometer apparatus.<br />

iv: The Ca 2+ , Mg 2+ , Na + , K + , Cl - , SO 2- 4 , <strong>and</strong> NO - 3 were determ<strong>in</strong>ed accord<strong>in</strong>g to Matiti (2004)<br />

v: The Heavy metals (Zn, Cu, Fe, Mn, Co, Cd, Ni, B, Cr, <strong>and</strong> Pb) <strong>and</strong> Boron were determ<strong>in</strong>ed us<strong>in</strong>g ICP-<br />

Perk<strong>in</strong> Elemer Model 4300DV.<br />

2.3 Water <strong>quality</strong> evaluation for irrigation<br />

The suitability <strong>of</strong> <strong>water</strong> <strong>resources</strong> <strong>in</strong> Riyadh <strong>and</strong> Al-Ahsa for irrigation was evaluated by FAO (Ayers <strong>and</strong><br />

Westcoat, 1985), U.S. sal<strong>in</strong>ity laboratory (Richard, 1954), <strong>and</strong> KSA (K<strong>in</strong>gdom <strong>of</strong> <strong>Saudi</strong> <strong>Arabia</strong>, 2003)<br />

methods.<br />

2.4 <strong>Hydrochemical</strong> facies<br />

The hydro-chemical characteristics <strong>of</strong> the m<strong>in</strong>eral <strong>water</strong> were evaluated by Piper diagram (Piper, 1944).<br />

2.5 Geochemical model<strong>in</strong>g<br />

Interaction between <strong>water</strong> <strong>and</strong> surround<strong>in</strong>g rocks <strong>and</strong> soil are considered to be the ma<strong>in</strong> processes controll<strong>in</strong>g<br />

the observed chemical characteristics. The deviation <strong>of</strong> <strong>water</strong> from equilibrium with respect to dissolved<br />

m<strong>in</strong>erals is quantitatively described by saturation <strong>in</strong>dex (SI). The SI <strong>of</strong> a m<strong>in</strong>eral is obta<strong>in</strong>ed from the<br />

follow<strong>in</strong>g formula:<br />

SI = log IAP/k t (1)<br />

where IAP is ion activity product <strong>of</strong> dissociated chemical species <strong>in</strong> solution <strong>and</strong> k t is the equilibrium solubility<br />

product <strong>of</strong> the chemical <strong>in</strong>volved (Alexakis, 2011).<br />

The hydro-geochemical equilibrium model, Phreeqc model (Parkhurst <strong>and</strong> Appelo, 1999), was used to<br />

calculate the SI <strong>of</strong> <strong>water</strong> with respect to the ma<strong>in</strong> m<strong>in</strong>eral phases.<br />

IAEES<br />

www.iaees.org

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