Rare earth element (REE) concentrations in river water reflect both local geological background and the intensity of anthropogenic activities. The increasing demand for high-tech applications is accompanied by an increase in REEs in water environments, especially in urban regions. Therefore, the dissolved REEs in a typical urban river (Yongding River) were analyzed to reveal the influence of anthropogenic inputs. It was found that the sum of dissolved REE (ΣREE) concentrations in river water were 6.27~86.26 ng L−1 (mean 31.05 ng L−1). The spatial distribution of REEs is significantly affected by both natural processes and human activities. To eliminate the effect of upstream land use on downstream measurements, this study established a 500 m buffer zone alongside the river and identified the anthropogenic origin of REEs through correlations among land use proportions within the buffer zone, the population density, and REEs. The Post-Archean Australian Shale (PAAS)-normalized REEs revealed pronouncedly positive Gd anomalies in the range 0.30~20.16 in all river samples. Spearman correlation analysis indicated that the proportion of cultivated land was positively correlated with most of the REEs. A three-dimensional tracer system was established via Gdanth, NO3−/Na+ and Cl−/Na+ to characterize the impact of sewage treatment plants, hospitals and agricultural activities on river water. The results indicate that with the acceleration of urbanization, abnormal REEs can be considered as a sensitive indicator to assess the influence of anthropogenic activities on water ecosystems.
Dissolved heavy metals (HMs), derived from natural and anthropogenic sources, are an important part of aquatic environment research and gain more international concern due to their acute toxicity. In this study, the geochemistry of dissolved HMs was analyzed in the upper Three Gorges Reservoir (TGR) of the Yangtze River (YZR) watershed to explore their distribution, status, and sources and further evaluate the water quality and HM-related risks. In total, 57 water samples were collected from the main channel and tributaries of the upper TGR. The concentrations of eight HMs, namely V, Ni, Cu, Zn, As, Mo, Cd, and Pb, were measured by ICP-MS. The mean concentrations (in μg/L) of eight HMs decreased in the order: As (1.46), V (1.44), Ni (1.40), Mo (0.94), Cu (0.86), Zn (0.63), Pb (0.03), and Cd (0.01). The concentrations of most HMs were 1.4~8.1 times higher than that in the source area of the YZR, indicating a potential anthropogenic intervention in the upper TGR. Spatially, the concentrations of V, Cu, As, and Pb along the main channel gradually decreased, while the others were relatively stable (except for Cd). The different degrees of variations in HM concentrations were also found in tributaries. According to the correlation analysis and principal component (PC) analysis, three PCs were identified and explained 75.1% of the total variances. combined with the concentrations of each metal, PC1 with high loadings of V, Ni, As, and Mo was considered as the main contribution of human inputs, PC2 (Cu and Pb) was primarily attributed to the contribution of mixed sources of human emissions and natural processes, and Zn and Cd in PC3 were controlled by natural sources. Water quality assessment suggested the good water quality (meeting the requirements for drinking purposes) with WQI values of 14.1 ± 3.4 and 11.6 ± 3.6 in the main channel and tributaries, respectively. Exposure risk assessment denoted that the health effects of selected HMs on the human body were limited (hazard index, HI < 1), but the potential risks of V and As with HI > 0.1 were non-negligible, especially for children. These findings provide scientific support for the environmental management of the upper TGR region and the metal cycle in aquatic systems.
As the largest and most representative tributary of the Mekong River, the Mun River Basin (MRB) provides critical understanding of regional hydro-geochemical features and rock weathering processes on a basin scale. The present study measured strontium (Sr) isotopes with hydro-geochemistry data of 56 water samples in detail in the MRB in northeast Thailand. The dissolved Sr contents and 87Sr/86Sr isotopic ratios were reported to be 8.7–344.6 μg/L (average 126.9 μg/L) and 0.7085–0.7281 (average 0.7156), respectively. The concentrations of dissolved Sr in the mainstream slightly decreased from upstream to downstream, while the variation trend of 87Sr/86Sr was on the contrary. Correlation analysis showed that Na+ strongly correlated with Cl− (0.995, p < 0.01), while Ca2+ exhibited weak relationships with SO42− (0.356, p < 0.01). Samples of the MRB exhibited lower Mg2+/Na+, Ca2+/Na+, HCO3−/Na+ and 1000Sr/Na ratios, and gathered around the end-member of evaporite dissolution, with slight shift to silicate weathering end-member, demonstrating the dominant contribution of evaporite dissolution and silicate weathering on dissolved loads. Comparing with data of major world rivers from previous research, our results remained consistency with rivers draining through similar geological conditions. The dissolved Sr flux to the adjacent Mekong River was estimated to be 20.7 tons/year. In accordance with the forward model, silicate weathering rate and CO2 consumption rate during dry season were calculated to be 0.73 tons/km2/year and 1.94 × 104 mol/km2/year, and may get underestimated due to intense water consumption by extensive agricultural activities. The superimposed effect of anthropogenic impacts on the water environment could enhance chemical weathering, and thus should be taken into account in regional ion cycles and carbon budgets. These findings highlight the coupling analysis of Sr isotopes and hydro-geochemistry in Earth surface processes and provide basic investigation for sustainable regional water treatment mechanisms in the pan basin of the Mekong River.
Air pollutants have been investigated in many studies, but the variations of atmospheric pollutants and their relationship with rainwater chemistry are not well studied. In the present study, the criteria atmospheric pollutants in nine monitoring stations and rainwater chemistry were analyzed in karst Guiyang city, since the time when the Chinese Ambient Air Quality Standards (CAAQS, third revision) were published. Based on the three-year daily concentration dataset of SO2, NO2, CO, PM10 and PM2.5, although most of air pollutant concentrations were within the limit of CAAQS III-Grade II standard, the significant spatial variations and relatively heavy pollution were found in downtown Guiyang. Temporally, the average concentrations of almost all air pollutants (except for CO) decreased during three years at all stations. Ratios of PM2.5/PM10 in non- and episode days reflected the different contributions of fine and coarse particles on particulate matter in Guiyang, which was influenced by the potential meteorological factors and source variations. According to the individual air quality index (IAQI), the seasonal variations of air quality level were observed, that is, IAQI values of air pollutants were higher in winter (worst air quality) and lower in summer (best air quality) due to seasonal variations in emission sources. The unique IAQI variations were found during the Chinese Spring Festival. Air pollutant concentrations are also influenced by meteorological parameters, in particular, the rainfall amount. The air pollutants are well scoured by the rainfall process and can significantly affect rainwater chemistry, such as SO42−, NO3−, Mg2+, and Ca2+, which further alters the acidification/alkalization trend of rainwater. The equivalent ratios of rainwater SO42−/NO3− and Mg2+/Ca2+ indicated the significant contribution of fixed emission sources (e.g., coal combustion) and carbonate weathering-influenced particulate matter on rainwater chemistry. These findings provide scientific support for air pollution management and rainwater chemistry-related environmental issues.
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