Small quantities of liquid water lining triple junctions in polycrystalline glacier ice form connected vein networks that enable material exchange with underlying basal environments. Diffuse debris concentrations commonly observed in ice marginal regions might be attributed to this mechanism. Following recent cryogenic ring-shear experiments, we observed emplacement along grain boundaries of loess particles several tens of microns in size. Here, we describe an idealized model of vein liquid flow to elucidate conditions favoring such particle transport. Gradients in liquid potential drive flow toward colder temperatures and lower solute concentrations, while deviations of the ice stress state from hydrostatic balance produce additional suction toward anomalously low ice pressures. Our model predicts particle entrainment following both modest warming along the basal interface resulting from anticipated natural changes in effective stress, and the interior relaxation of temperature and solute concentration imposed by our experimental protocols. Comparisons with experimental observations are encouraging, but suggest that liquid flow rates are somewhat higher and/or more effective at dragging larger particles than predicted by our idealized model with nominal parameter choices. Diffuse debris entrainment extending several meters above the glacier bed likely requires a more sophisticated treatment that incorporates effects of ice deformation or other processes.

We report detailed chemical and isotopic data from a subglacial siliceous deposit on andesitic bedrock recently exposed by glacier retreat. Whereas a single, <1 μm, Si-rich layer covers the highly polished bedrock on the up-glacier (stoss) surfaces, distinct, lithified deposits commonly occur at the lee of small bedrock protuberances, on a scale <0.1 meter. The deposit is millimeters in thickness and consists of laminae tens to hundreds microns thick that differ from one another in color, rock-fragment abundance and chemical composition. Ca-rich laminae that are sufficiently enriched in uranium (~2–50 ppm) to permit U-series isotopic analysis suggest that the subglacial deposit formed 10–20 ka, much earlier than previously assumed. We conclude that (1) the siliceous deposit persisted for at least 10 000 years despite the intervening erosion and weathering, (2) distinct episodes of formation due to significant changes in hydrology and water chemistry are recorded in the deposit, and (3) a siliceous slurry may have existed at the ice-rock interface and influenced the local friction. This work reinforces earlier findings that subglacial chemical deposits can form and persist on geologic time scales and may have implications for the role of the cryosphere in the Earth's geochemical cycles and climate system.

The subglacial chemical weathering environment is largely controlled by low temperatures and the presence of freshly comminuted minerals with a high surface area. These characteristics are believed to promote dissolution processes that give rise to low silica and high Ca2+ fluxes emanating from glacierized basins. We test an alternative hypothesis, that mineral precipitation reactions in the subglacial environment play an equally important role in controlling the water chemistry in glacierized basins. We analyze borehole and proglacial water chemistry from a subarctic polythermal glacier, complemented by mineral XRD analysis of suspended sediment, till and bedrock samples. In conjunction with a thermodynamic analysis of the water and mineral chemistry, we use reaction-path modelling to study the chemical enrichment of water through the glacier system. We find that the high pH of the subglacial environment is conducive to secondary mineral precipitation, and that it is not possible to balance the water chemistry using dissolution reactions alone. We show that low silica can be explained by standard weathering reactions without having to invoke mineral-leaching reactions. Our results suggest that subglacial weathering intensity may be significantly underestimated if the production of secondary minerals is not considered.