Drinking water quality is a major concern, especially in African countries. This manuscript aims to analyze the chemical composition of Lioua’s groundwater in order to determine the geological processes influencing the chemical elements' composition and origin. Therefore, chemometrics techniques such as multivariate statistical analysis (MSA) and time series methods (TSM) are used. Indeed, MSA includes a component analysis (PCA) and a cluster analysis (CA), while au-tocorrelation analysis (AA) supplemented by simple spectral density analysis (SDA) is used for TMS. PCA displays three main factors explaining a total variance (TV) of 85.01 %. Factors 1, 2, and 3 are 68.72%, 11.96%, and 8.89 % of TV, respectively. In the CA, three groups were controlled by TDS and EC. G1 reveals a close association between SO42−, K+, Ca2+, and TDS; G2 reveals a close association between Na+, Cl−, Mg2+, and EC; G3 shows the dissociation of bicarbonates HCO3− and NO3− from other chemical elements. AA shows a linear interrelationship of EC, Mg2+, Na+, K+, Cl−, and SO42−. However, NO3− and HCO3− indicate uncorrelated characteristics with other parameters. For SDA, the correlograms of Mg2+, Na+, K+, Cl−, and SO42− have a similar trend with EC. None-theless, pH, Ca2+, HCO3− and NO3− exhibit multiple peaks related to the presence of several dis-tinct cyclic mechanisms. The methods enabled the authors to conclude that the geochemical processes influencing the chemical composition are: (i) dissolution of evaporated mineral depos-its, (ii) water-rock interaction, and (iii) evaporation process. In addition, Groundwater exhibits two bipolar characteristics, one recorded with negative and positive charges on pH and Ca+ and another recorded only with negative charges on HCO3− and NO3−. On the other hand, SO42-, K+, Ca2+, and TDS are the major predominant elements in the groundwater’s chemical composition. The major participation of salts and chlorides is in the electrical conductivity of water. The dominance of the lithological factor in the overall mineralization of the Plio-Quaternary surface aquifer waters. The origins of HCO3− and NO3− are different. Indeed, carbonated for HCO3- has a carbonate origin, whereas NO3– has an anthropogenic origin. The salinity was affected by Mg2+, SO42-, Cl-, Na+, K+, and EC. Ca2+, HCO3− and NO3− are resulted from human activity fertilizers, the carbonate facies outcrops, and domestic sewage.