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The residence time of subglacial meltwater impacts aquifer recharge, nutrient production, and chemical signals that reflect underlying bedrock/substrate, but is inaccessible to direct observation. Here we report the seasonal evolution of subglacial meltwater chemistry from the 2011 melt season at the terminus of the Athabasca Glacier, Canada. We measured major and trace analytes and U-series isotopes for twenty-nine bulk meltwater samples collected over the duration of the melt season. This dataset, which is the longest time-series record of ( 234 U/ 238 U) isotopes in a glacial meltwater system, provides insight into the hydrologic evolution of the subglacial system during active melting. Meltwater samples, measured from the outflow, were analyzed for ( 238 U), ( 222 Rn) and ( 234 U/ 238 U) activity , conductivity, alkalinity, pH and major cations. Subglacial meltwater varied in [ 238 U] and ( 222 Rn) from 23 to 832 ppt and 9 to 171 pCi/L, respectively. Activity ratios of ( 234 U/ 238 U) ranged from 1.003 to 1.040, with the highest ( 238 U), ( 222 Rn) and ( 234 U/ 238 U) activity values occurring in early May when delayed-flow basal meltwater composed a significant portion of the bulk melt. From the chemical evolution of the meltwater, we posit that the relative subglacial water residence times decrease over the course of the melt season. This decrease in qualitative residence time during active melt is consistent with prior field studies and model-predicted channel switching from a delayed, distributed network to a fast, channelized network flow. As such, our study provides support for linking U-series isotopes to storage lengths of meltwater beneath glacial systems as subglacial hydrologic networks evolve with increased melting and channel network efficiency.

The Upper Fremont Glacier (UFG), Wyoming, is one of the few continental glaciers in the contiguous United States known to preserve environmental and climate records spanning recent centuries. A pair of ice cores taken from UFG have been studied extensively to document changes in climate and industrial pollution (most notably, mid-19th century increases in mercury pollution). Fundamental to these studies is the chronology used to map ice-core depth to age. Here, we present a revised chronology for the UFG ice cores based on new measurements and using a novel dating approach of synchronizing continuous water isotope measurements to a nearby tree-ring chronology. While consistent with the few unambiguous age controls underpinning the previous UFG chronologies, the new interpretation suggests a very different time scale for the UFG cores with changes of up to 80 years. Mercury increases previously associated with the mid-19th century Gold Rush now coincide with early-20th century industrial emissions, aligning the UFG record with other North American mercury records from ice and lake sediment cores. Additionally, new UFG records of industrial pollutants parallel changes documented in ice cores from southern Greenland, further validating the new UFG chronologies while documenting the extent of late 19th and early 20th century pollution in remote North America.

Over the past ~ 5000 years, amplified dust generation and deposition in the American West has been linked to human activity. In recent decades, intensified rates of agriculture and livestock grazing have been correlated with greater dust production detected on seasonal to annual timescales. The combination of land use intensification and climate change (i.e. increased drought frequency) in North America highlights the importance of characterizing the sources of dust both before and after the influence of anthropogenic activity. We apply high-precision geochemical and isotopic (Sr and Nd isotopes) techniques to an ice core from the Upper Fremont Glacier (Wyoming, USA) to produce the first glacial dataset from the American West. Our Sr-Nd isotopic composition data indicates the evolving dust provenance to the Upper Fremont Glacier (UFG) from a long-range transport of mineral dust to a local source. This increasing input of dust from a local source is supported by a rise in average dust particle diameter combined with greater average dust concentration throughout the record. The greater presence of dust particles smaller than 2.5 μm in the most recent samples from UFG ice core record support existing satellite and sediment core data regarding the effects of anthropogenic activity upon dust sources and pathways in the American West. Although the Sr-Nd isotope database in North America needs be expanded, our results provide a survey of windborne dust through the past 270 years.

Changes in the composition of dust trapped in ice provide evidence of past atmospheric circulation and earth surface conditions. Investigations of dust provenance in Antarctic ice during glacial and interglacial periods indicate that South America is the primary dust source during both climate regimes. Here, we present results from a new ice core dust archive extracted from the Taylor Glacier in coastal East Antarctica during the deglacial transition from Marine Isotope Stage 6 to 5e. Radiogenic strontium and neodymium isotopes indicate that last interglacial dust is young and volcanic, in contrast to the observed preindustrial and Holocene (Marine Isotope Stage 1) dust composition. The dust composition differences from the last interglacial and current interglacial period at the site require a profound difference in atmospheric transport and environmental conditions. We consider several potential causes for enhanced transport of volcanic material to the site, including increased availability of volcanic material and large-scale atmospheric circulation changes.