Hydrogeochemistry of naturally occurring arsenic in the Central Bolivian Altiplano

Defense of PhD thesis

Time: Thursday 2015-06-11 at 13:00

Place: Room V1, Teknikringen 76, KTH

Subject area: Land and water resources engineering

Respondent: Muricio Rodolfo Ormachea Munoz

Opponent: Professor M.E. Donselaar, Delft University of Technology

Main supervisor: Professor Prosun Bhattacharya

The research project was hosted by the Division of Land and Water Resources Engineering , SEED Department, KTH. A link to the dissertation can be found here .

Abstract

The Bolivian Altiplano (BA) is a high plateau located in the western part of the country at an altitude of 3,600 to 3,900 meters above sea level and is bordered by the Eastern and Western Cordillera. Within the BA there is a large endorheic hydrologic system linking the Titicaca Lake in the north the Desaguadero River, lakes Uru-Uru and Poopó in the central part; and the Lacajahuira River and Coipasa and Uyuni salt pans in the south. Several mineralized areas, especially in the Eastern Cordillera, have been intensively exploited for centuries for the extraction of silver, gold, and tin from polymetallic sulfide ore deposits. Presently many urban centers are also contributing for an extensive contamination in localized areas; especially the Poopó Lake and some rivers are affected by high loads of wastewater and solid waste, in addition to the release of heavy metals and arsenic (As) due to acid mine drainage

The presence of As in the BA was known to be related to mining only, but recent studies revealed that As of geogenic origin also contributing to the elevated concentration of As in surface and groundwater. The Poopó Lake basin is characterized by a semiarid climate. Geologic formations predominantly are of volcanic origin and groundwater flow is sluggish in nature. These environmental settings have generated substantially elevated concen- trations of geogenic As and other trace elements in surface and groundwater. Both surface and groundwater used for drinking water have high concentrations of As that by far exceed the World Health Organization (WHO) guideline. The overall objective of the present study has been focused on the determination of the sources and principal mechanisms for mobilization of geogenic As into surface and groundwater of the Poopó Lake basin area. More specifically, this study has determined the spatial distribution and the extent of As contamination in surface and groundwater; chemical composition of surface and groundwater, rock and sediment; major geochemical mechanisms for As mobilization from solid phase to aqueous phases. This study also made an assessment of drinking water quality in rural areas within the Poopó Lake basin.

Arsenic concentration exceeded the WHO guideline and national regulations for drinking water of 10 µg/L in 85% of the samples collected from the area around the Poopó Lake (n=27) and 90% of the samples from the southern part of the lake basin (n=42). Groundwater samples collected from drinking water wells had As concentrations up to 623 µg/L, while samples collected from piezometers had even higher up to 3,497 µg/L. Highest concentration in river water samples was observed 117 µg/L. Alkaline nature of water (median pH 8.3 for groundwater and 9.0 for surface water), predominance of Na-Cl-HCO₃ water type and elevated Eh reflecting oxidized character has been revealed by As(V) as the major species in As speciation. Different rock types were analyzed for their As content and the highest concentration of 27 mg/kg was found in a coral limestone sample. In evaporate it was 13 mg and 11 mg As/kg was measured in calcareous sandstone. Elevated concentration of As was also observed in sediment cores collected from two drilling sites; 51 mg/kg in Condo K and 36 mg/kg in Quillacas. Physical and chemical weathering of volcanic rocks, limestone, carbonates and plagioclase minerals enhance the supply of Na⁺ and HCO₃^- into solution and as a consequence pH and alkalinity increase, which in turn, favor As desorption from solid mineral surfaces (especially Fe(III) oxyhydr- oxides) and therefore dissolved As in water is increased.