Hydrochemistry of the Lhasa River, Tibetan Plateau: Spatiotemporal Variations of Major Ions Compositions and Controlling Factors Using Multivariate Statistical Approaches

Spatiotemporal variations of the hydrochemical major ions compositions and their controlling factors are essential features of a river basin. However, similar studies in the southern Tibetan Plateau are relatively limited. This study focuses on the chemical compositions of the dissolved loads in the Lhasa River (LR) in the southern Tibetan Plateau. Two sampling campaigns were conducted during the rainy and dry seasons across the LR basin to systematically investigate the spatiotemporal variations of water chemistry and sources of the dissolved loads. The results show that the river water possesses slight alkalinity with an average pH of 8.05 ± 0.04. Total dissolved solids (TDS) and oxidation-reduction potential (ORP) range widely from 39.8 mg/L to 582.6 mg/L with an average value of 165.6 ± 7.7 mg/L and from −9.4 mV to 295 mV with a mean value of 153.7 ± 6.9 mV, respectively. The major cations follow the decreasing order of Ca²⁺, Mg²⁺, Na⁺, and K⁺ while HCO₃⁻, SO₄²⁻, Cl⁻, and NO₃⁻ for anions. Ca²⁺ and Mg²⁺ account for 87.8% of the total cations, while HCO₃⁻ and SO₄²⁻ accounts for 93.9% of the total anions. All the major ions show higher concentrations in the dry season. NO₃⁻, HCO₃⁻, and Mg²⁺ show significant spatial variations due to the influence of basin lithology and anthropogenic activity. Multi-variables statistical analysis reveals that the mechanisms controlling the LR hydrochemistry are mainly carbonate weathering followed by silicate weathering. Geothermal springs and anthropogenic activities also play crucial roles in altering river water ions composition in the middle stream and downstream. The relatively high NO₃⁻ value (3 ± 0.2 mg/L) suggests water quality will be under the threat of pollution with the increase of anthropogenic activities. View Full-Text