Most studies on the weathering of mine waste rock focus on the generation of acidic drainage with high metal concentrations, whereas metal(loid) release under neutral-rock drainage (NRD) conditions has received limited attention. Here, we present geochemical and mineralogical data from a long-term (>10 years) kinetic testing program with 50 waste-rock field barrels at the polymetallic Antamina mine in Peru. The weathering of most rock lithologies in the field experiments generated circumneutral to alkaline drainage (6 < pH < 9) but with concentrations of the oxyanion-forming metal(loid)s As, Mo, Se, and Sb in the mg/L range. The mobilization of As and Sb was particularly efficient from intrusive, marble and hornfels rocks that contained labile As- and Sb-sulfides, irrespective of bulk elemental content or waste-rock reactivity. High-alkalinity drainage from these materials sustained neutral-pH conditions that are unfavorable to oxyanion adsorption onto Fe-(oxyhydr)oxides and, therefore, enhanced As and Sb leaching. The release of Mo and Se from sulfidic skarn and intrusive waste rock was more proportional to elemental content but equally enhanced by pH-inhibited adsorption and negligible secondary mineral precipitation under NRD conditions. Our results demonstrate that oxyanion concentrations of environmental concern may be conveyed by neutral- to alkaline-pH waste-rock drainage and should be a focus of mine wastewater monitoring programs.

Research in geocryology is currently principally concerned with the effects of climate change on permafrost terrain. The motivations for most of the research are (1) quantification of the anticipated net emissions of CO₂ and CH₄ from warming and thaw of near‐surface permafrost and (2) mitigation of effects on infrastructure of such warming and thaw. Some of the effects, such as increases in ground temperature or active‐layer thickness, have been observed for several decades. Landforms that are sensitive to creep deformation are moving more quickly as a result, and Rock Glacier Velocity is now part of the Essential Climate Variable Permafrost of the Global Climate Observing System. Other effects, for example, the occurrence of physical disturbances associated with thawing permafrost, particularly the development of thaw slumps, have noticeably increased since 2010. Still, others, such as erosion of sedimentary permafrost coasts, have accelerated. Geochemical effects in groundwater from trace elements, including contaminants, and those that issue from the release of sediment particles during mass wasting have become evident since 2020. Net release of CO₂ and CH₄ from thawing permafrost is anticipated within two decades and, worldwide, may reach emissions that are equivalent to a large industrial economy. The most immediate local concerns are for waste disposal pits that were constructed on the premise that permafrost would be an effective and permanent containment medium. This assumption is no longer valid at many contaminated sites. The role of ground ice in conditioning responses to changes in the thermal or hydrological regimes of permafrost has re‐emphasized the importance of regional conditions, particularly landscape history, when applying research results to practical problems.

We investigated geochemical processes controlling uranium release in neutral-pH (pH ≥ 6) rock drainage (NRD) at a prospective gold deposit hosted in granite, schist, and gneiss. Although uranium is not an economic target at this deposit, it is present in the host rock at a median abundance of 3.7 µg/g, i.e., above the average uranium content of the Earth’s crust. Field bin and column waste-rock weathering experiments using gneiss and schist mine waste rock produced circumneutral-pH (7.6 to 8.4) and high-alkalinity (41 to 499 mg/L as CaCO₃) drainage, while granite produced drainage with lower pH (pH 4.7 to >8) and lower alkalinity (<10 to 210 mg/L as CaCO₃). In all instances, U release was associated with calcium release and formation of weakly sorbing calcium-carbonato-uranyl aqueous complexes. This process accounted for the higher release of uranium from carbonate-bearing gneiss and schist than from granite despite the latter’s higher solid-phase uranium content. In addition, unweathered carbonate-bearing rocks having a higher sulfide-mineral content released more uranium than their oxidized counterparts because sulfuric acid produced during sulfide-mineral oxidation promoted dissolution of carbonate minerals, release of calcium, and formation of calcium-carbonato-uranyl aqueous complexes. Substantial uranium attenuation occurred during a sequencing experiment involving application of uranium-rich gneiss drainage into columns containing Fe-oxide rich schist. Geochemical modeling indicated that uranium attenuation in the sequencing experiment could be explained through surface complexation and that this process is highly sensitive to dissolved calcium concentrations and pCO₂ under NRD conditions.

Uranium (U) contamination in groundwater from geogenic sources affects water quality globally. Here, we use a multifaceted isotopic and geochemical approach to elucidate U sources and controls on geogenic U release to groundwater and surface water at a prospective subarctic gold deposit in Yukon, Canada, that is characterized by permafrost, fractured bedrock, and cold (<2 °C) groundwater. X-ray absorption spectroscopy, sequential extractions, and micro X-ray fluorescence mapping show extensive subsurface oxidation and solid-phase U present in its hexavalent and mobile form. Limited ²³⁸U/²³⁵U isotope fractionation and predominance of U(VI) in rocks suggest U(VI) sorption–desorption is the main driver of U mobilization. Groundwater U concentrations are appreciable (median 38 μg/L, range 1.2–535 μg/L) and are explained by high-alkalinity, Ca-rich groundwater produced from oxidative weathering of sulfide and carbonate-mineralized structures around the deposit. Minor ²³⁸U/²³⁵U isotope fractionation in groundwater indicates that limited U(VI) reduction occurs beneath permafrost despite groundwater redox conditions below Fe(III) and S(VI) reduction, and groundwater ages inferred from ³H and ¹⁴C to be on the order of thousands of years. The complexation of U as uranyl–calcium–carbonate complexes and the resilience of these complexes to U(VI) reduction contributes to high U(VI) mobility under cold groundwater conditions. This study provides insight into processes and time scales of U transport in subarctic groundwater at a pivotal time when hydrogeochemical changes may be anticipated in cold regions worldwide due to permafrost degradation.