The stable isotope composition of waters (
2H,
18O) canbe used as a natural tracer of hydrologic processes insystems affected by acid mine drainage. We in
vestigatedthe
2H and
18O
values of pore waters from four oxidizingsulfidic mine tailings impoundments in different climaticregions of Chile (Piuquenes at La Andina with Alpine climate,Cauquenes and Car&
eacute;n at El Teniente with Mediterraneanclimate, and Talabre at the Chuquicamata deposit withhyperarid climate). No clear relationship was found betweenaltitude and isotopic composition. The obser
ved displacementof the tailings pore waters from the local meteoricwater line toward higher
18O
values (by ~ +2
18Orelati
ve to
2H) is partly due to water-rock interactionprocesses, including hydration and O-isotope exchange withsulfates and Fe(III) oxyhydroxides produced by pyriteoxidation. In most tailings, from the saturated zone towardthe surface, isotopically different zones can be distinguished.Zone I is characterized by an upward depletion of
2Hand
18O in the pore waters from the saturated zone andthe lowermost
vadose zone, due to ascending diffusedisotopically light water triggered by the constant loss ofwater
vapor by e
vaporation at the surface. In zone II, thecapillary flow of a mix of
vapor and liquid water causesan e
vaporati
ve isotopic enrichment in
2H and
18O. At the topof the tailings in dry climate a zone III between thecapillary zone and the surface contains isotopically lightdiffused and atmospheric water
vapor. In temperate climates,the upper part of the
profile is affected by recent rainfalland zone III may not differ isotopically from zone II.