Spatial dependency of arsenic, antimony, boron and other trace elements in the shallow groundwater systems of the Lower Katari Basin, Bolivian Altiplano.

Spatial patterns, cluster or dispersion trends are statistically different from random patterns of trace elements (TEs), which are essential to recognize, e.g., how they are distributed and change their behavior in different environmental processes and/or in the polluted/contaminated areas caused by urban and industrial pollutant located in upstream basins and/or by different natural geological conditions. The present study focused on a statistical approach to obtain the spatial variability of TEs (As, B and Sb) in shallow groundwater (GW) in a high-altitude arid region (Lower Katari Basin, Bolivian Altiplano), using multivariate analysis (PCA and HCA), geochemical modeling (PHREEQC, MINTEQ) and spatial analyses (Moran's I and LISA), considering the community supply wells. The results indicate that despite of the outliers there is a good autocorrelation in all cases, since Moran's I values are positive. The global spatial dependence analysis indicated a positive and statistically significant spatial autocorrelation (SA) for all cases and TEs are not randomly distributed at 99% confidence level. The results of hydrochemical modeling suggested the precipitation and stability of Fe (III) phases such as goethite. The re-adsorption of As and Sb on the mineral surface in the aquifer could be limiting the concentrations of both metalloids in southern regions. Spatial autocorrelation was positive (High-High) in northwestern (arsenic), southeastern (boron) and northeastern (antimony) region. The results reflected that the As and Sb are the main pollutants linked to the natural geological conditions, but B is a main pollutant due to the anthropogenic activities. Furthermore, >50% shallow groundwater exceeded the WHO limit and NB-512 guideline values for Sb (87%), B (56%) and As (50%); therefore the spatial distribution and concentrations of these TEs in GW raise a significant concern about drinking water quality in the study area.

Contrasting controls on hydrogeochemistry of arsenic-enriched groundwater in the homologous tectonic settings of Andean and Himalayan basin aquifers, Latin America and South Asia.

High groundwater arsenic (As) across the globe has been one of the most well researched environmental concerns during the last two decades. Consequently, a large scientific knowledge-base has been developed on As distributions from local to global scales. However, differences in bulk sediment As concentrations cannot account for the As concentration variability in groundwater. Instead, in general, only aquifers in sedimentary basins adjacent to mountain chains (orogenic foreland basins) along continental convergent tectonic margins are found to be As-enriched. We illustrate this association by integrating observations from long-term studies of two of the largest orogenic systems (i.e., As sources) and the aquifers in their associated foreland basins (As sinks), which are located in opposite hemispheres and experience distinct differences in climate and land-use patterns. The Andean orogenic system of South America (AB), an active continental margin, is in principle a modern analogue of the Himalayan orogenic system associated with the Indus-Ganges-Brahmaputra river systems in South Asia (HB). In general, the differences in hydrogeochemistry between AB and HB groundwaters are conspicuous. Major-solute composition of the arid, oxic AB groundwater exhibits a mixed-ion hydrochemical facies dominated by Na-Ca-Cl-SO4-HCO3. Molar calculations and thermodynamic modeling show that although groundwater of AB is influenced by cation exchange, its hydrochemical evolution is predominated by feldspar dissolution and relationships with secondary clays. In contrast, humid, strongly reducing groundwater of HB is dominated by Ca-HCO3 facies, suggestive of calcite dissolution, along with some weathering of silicates (monosiallitization). This work demonstrates that although hydrogeochemical evolutionary trends may vary with local climate and lithology, the fundamental similarities in global tectonic settings can still lead to the elevated concentrations of groundwater As.

Fractionation of heavy metals and assessment of contamination of the sediments of Lake Titicaca.

Chemical weathering is one of the major geochemical processes that control the mobilization of heavy metals. The present study provides the first report on heavy metal fractionation in sediments (8-156 m) of Lake Titicaca (3,820 m a.s.l.), which is shared by the Republic of Peru and the Plurinational State of Bolivia. Both contents of total Cu, Fe, Ni, Co, Mn, Cd, Pb, and Zn and also the fractionation of these heavy metals associated with four different fractions have been determined following the BCR scheme. The principal component analysis suggests that Co, Ni, and Cd can be attributed to natural sources related to the mineralized geological formations. Moreover, the sources of Cu, Fe, and Mn are effluents and wastes generated from mining activities, while Pb and Zn also suggest that their common source is associated to mining activities. According to the Risk Assessment Code, there is a moderate to high risk related to Zn, Pb, Cd, Mn, Co, and Ni mobilization and/or remobilization from the bottom sediment to the water column. Furthermore, the Geoaccumulation Index and the Enrichment Factor reveal that Zn, Pb, and Cd are enriched in the sediments. The results suggest that the effluents from various traditional mining waste sites in both countries are the main source of heavy metal contamination in the sediments of Lake Titicaca.