Over the last two decades, anomalous warming events have been observed in coastal Antarctic regions. While these events have been documented in the Ross Sea sector, the Antarctic interior is believed to have been buffered from warming. In this work, we present data from lakes located near Mt. Heekin and Thanksgiving Valley (~85° S) along the Shackleton Glacier, which are believed to be the southern-most Antarctic dry valley lakes. In 2018, the lakes were characterized, repeat satellite images were examined, and lake water chemistry was measured. Our analysis shows that lake areas recently increased, and the water-soluble ion chemistry indicates a flushing of salts from periglacial soils, likely from increased glacial melt as illustrated by water isotope data. Our results show that high southern latitude ice-free areas have likely been affected by warm pulses over the past 60 years and these pulses may be quasi-synchronous throughout the Transantarctic Mountains.

The Subglacial Antarctic Lakes Scientific Access (SALSA) Project accessed Mercer Subglacial Lake using environmentally clean hot-water drilling to examine interactions among ice, water, sediment, rock, microbes and carbon reservoirs within the lake water column and underlying sediments. A ~0.4 m diameter borehole was melted through 1087 m of ice and maintained over ~10 days, allowing observation of ice properties and collection of water and sediment with various tools. Over this period, SALSA collected: 60 L of lake water and 10 L of deep borehole water; microbes >0.2 μm in diameter from in situ filtration of ~100 L of lake water; 10 multicores 0.32–0.49 m long; 1.0 and 1.76 m long gravity cores; three conductivity–temperature–depth profiles of borehole and lake water; five discrete depth current meter measurements in the lake and images of ice, the lake water–ice interface and lake sediments. Temperature and conductivity data showed the hydrodynamic character of water mixing between the borehole and lake after entry. Models simulating melting of the ~6 m thick basal accreted ice layer imply that debris fall-out through the ~15 m water column to the lake sediments from borehole melting had little effect on the stratigraphy of surficial sediment cores.

Polar subglacial hydrologic systems have garnered much interest since the recognition of Lake Vostok in 1996. In Antarctica, these environments are hydrologically diverse, including isolated lakes of different sizes, river–lake flow-through systems, “swamps” and groundwater (Siegert 2016). The refreezing of subglacial meltwater is also an important process beneath a large portion of the East Antarctic Ice Sheet (Bell et al. 2011). As subglacial water refreezes it exsolves salts, potentially leaving behind saline and hypersaline brines. Brines thought to derive from this cryoconcentration process have been observed in the northern polar permafrost regions and in the McMurdo Dry Valleys (MDVs) region of Antarctica. Additionally, sediments in the Victoria Land Basin have diagenetic signatures produced by brine movement dating from 3–11 m.y.a, suggesting hypersaline brines have existed in the McMurdo region since at least this time (Staudigel et al. 2018).

The stable-isotopic signature of dissolved inorganic carbon (DIC) has been routinely used in temperate lake systems to investigate the biogeochemical dynamics of carbon. We studied seven perennially ice-covered lakes in the McMurdo Dry Valleys, Antarctica, to ascertain how carbon cycling affects the δ13C of DIC in water columns of these systems. Unlike temperate lakes and, in fact, most polar lake systems, the permanent ice covers of these lakes eliminate physical mixing (turnover) and hence redistribution of DIC in the lakes, as well as minimize CO2 exchange with the atmosphere. These important and unique physical constraints have significant impact on carbon dynamics in the lakes, and important consequences for the δ13C distribution. The geochemistry in these lakes is influenced in varying amounts by landscape position, hydrologic input and their evolutionary history. Five of these lakes (both lobes of Lake Bonney, and Lakes Fryxell, Miers and Vanda) have surface water δ13C ratios of 0–4‰, Lake Hoare has more negative values, while Lake Joyce, the highest-elevation lake, has a much higher value (10.5‰). All of the lakes have upper- to mid-depth δ13C maxima reflecting biological uptake of 12C. Only four of the lakes (Lakes Vanda, Joyce, Hoare and Fryxell) have deep waters with negative values of δ13C, implying rigorous remineralization of 12C at depth. Lake Miers, the only lake that is not closed basin, has the smallest δ13C variation with depth, indicating that hydrologic exchange greatly influences the δ13C signal.

This paper reports the lead concentration and flux (where accumulation rate is available) along the route of the 1990 International Trans-Antarctic Expedition. The lead concentration in Larsen Ice Shelf and Antarctic Peninsula, the western part of the route, was 7.4 ± 4.1 pg g−1. The lead concentration in East Antarctic snow (South Pole to Mirny station) was 2 3 times higher than that in West Antarctica (Larsen Ice Shelf to South Pole). Taking into account the difference in site conditions, the difference between the above value over this area in 1989 and the value of 6.3 ±3.3 pg g−1 at a site within this area in 1980 (Wolff and Peel, 1985) is not significant. Because the relative contribution of soil dust, volcanoes and the oceans to lead concentration in Antarctica is about 0.5 pg g−1 under modern climatic conditions (Boutron and Patterson, 1987), it is believed that the lead in Antarctic surface snow is dominated by pollution input. The lead-concentration increase from west to east over the trans-Antarctic route suggests that remote Antarctica has been impacted by anthropogenic activities. The lowest lead flux (0.064 ng cn-2 a−1) was on the Antarctic Plateau, mainly reflecting the background global pollution. The mean flux of 0.273 ng cnT2 a−1 in the western part of the route (Larsen Ice Shelf to the Ellsworth Mountains) may result from the pollution input from the Southern Hemisphere. In addition to the influence of global and/or hemispheric pollution, local activities (notably the use of leaded gasolene) appear to have affected the region from Pionerskaya to Mirny.

Variations in the chemical composition of subsurface runoff within Canada Glacier, Antarctica, are used to identify the main source waters, which are vertical surfaces, and melt from solar-heated debris within channels, cryoconite holes and pools. The main flow paths are subsurface connections between cryoconite holes, pools and riffles. The latter may become partially disconnected during hard freeze. The chemical composition of runoff at the outlet of Canada Glacier during January 2000 was dominated by Ca2+, HCO3– and sea salt (Na+ and Cl–), and became depleted in sea-salt and non-sea-salt (*) SO42– as the subsurface drainage system in a frozen pool-and-riffle system was flushed and the melting ice surface became depleted of overwinter dry deposited salts. Only during 2 days of hard freeze did sea salt and *SO42– increase in concentration together. Otherwise, sea salt and *SO42– declined while *Ca2+ and HCO3– increased. The latter ions are derived from the chemical weathering of sediment in frozen-topped pools, channels and cryoconite holes. It is inferred that the hydrochemical processes which occur in the vestigial, subsurface drainage system are the elution of ions from ice melt, dilution of these ions downstream by ice melt from vertical surfaces and the dissolution of dust, in subsurface pools, channels and/or cryoconite holes.

The 2001/02 austral summer was the warmest summer on record in Taylor Valley, Antarctica, (∼78° S) since continuous records of temperature began in 1985. The highest stream-flows ever recorded in the Onyx River, Wright Valley, were also recorded that year (the record goes back to the 1969/70 austral summer). In early January 2002, a groundwater seep was observed flowing in the southwest portion of Taylor Valley. This flow has been named ‘Wormherder Creek’ (WHC) and represents an unusual event, probably occurring on a decadal time-scale. The physical characteristics of this feature suggest that it may have flowed at other times in the past. Other groundwater seeps, emanating from the north-facing slope of Taylor Valley, were also observed. Little work has been done previously on these very ephemeral seeps, and the source of water is unknown. These features, resembling recently described features on Mars, represent the melting of subsurface ice. The Martian features have been interpreted as groundwater seeps. In this paper we compare the chemistry of the WHC groundwater seep to that of the surrounding streams that flow every austral summer. The total dissolved solids content of WHC was ∼6 times greater than that of some nearby streams. The Na : Cl and SO4 : Cl ratios of the seep waters are higher than those of the streams, but the Mg : Cl and HCO3 : Cl ratios are lower, indicating different sources of solutes to the seeps compared to the streams. The enrichment of Na and SO4 relative to Cl may suggest significant dissolution of mirabilite within the previously unwetted soil. The proposed occurrence of abundant mirabilite in higher-elevation soils of the dry valley region agrees with geochemical models developed, but not tested, in the late 1970s. The geochemical data demonstrate that these seeps could be important in ‘rinsing’ the soils by dissolving and redistributing the long-term accumulation of salts, and perhaps improving habitat suitability for soil biota. The H4SiO4 concentration is 2–3 times greater in WHC than in the surrounding streams, indicating a large silicate-weathering component in the seep waters.

One of the unusual features of Lakes Fryxell and Hnare in Taylor Valley, southern Victoria Land, Antarctica, is their perennial ice cover. This ice cover limits gas exchange between the atmosphere and the lake water, and causesa very stable stratification of the lakes. We analyzed a series of water samples from profiles of these lakes and their tributaries for δ13C of the dissolved inorganic carbon (DIC) in order to qualify the carbon flux from the streams into the lakes, and to investigate the carbon cycling with in the lakes. Isotopic values in the uppermost waters (δ13C = +l.3‰ to 5.3‰ in Lake Hoare, +0.4‰ to +3.0‰ in Lake Fryxell) are close to the carbon-isotope values encountered in the streams feeding Lake Fryxell, but distinctively heavier than in streams feeding Lake Hoare (δ13C= — 2.3%n to 1.4%). These ratios are much heavier than ratios found in the moat that forms around the lakes injanuary February (δC = -10.1%). in the oxic photic zones of the lakes, photosynthesis clearly influences the isotopic composition, with layers of high productivity having enriched carbon-isotope signatures δ13C= +2.7‰ to +6.1‰). in both lakes, the isotopic values become lighter with depth, reaching minima of 3.2‰ and 4.0% in Lakes Fryxell and Hoare, respectively. These minima are caused by the microbial remineralization of isotopically light organic carbon. We present DIC flux calculations that help to interpret the isotopic distribution. For example, in Lake Hoare the higher utilization of CO2aq, and a substantially smaller inflow of CO2 from streams cause the heavier observed isotopic ratios. Differences in the hydrology and stream morphologies of the tributaries also greatly influence the carbon budgets of the basins.

The surface waters of the Southern Ocean play a key role in the global climate and carbon cycles by promoting growth of some of the world’s largest phytoplankton blooms. Several studies have emphasized the importance of glacial and sediment inputs of Fe that fuel the primary production of the Fe-limited Southern Ocean. Although the fertile surface waters along the shelf of the western Antarctic Peninsula (WAP) are influenced by large inputs of freshwater, this freshwater may take multiple pathways (e.g. calving, streams, groundwater discharge) with different degrees of water-rock interactions leading to variable Fe flux to coastal waters. During the summers of 2012–13 and 2013–14, seawater samples were collected along the WAP, near Anvers Island, to observe water column dynamics in nearshore and offshore waters. Tracers (223,224Ra, 222Rn, 18O, 2H) were used to evaluate the source and transport of water and nutrients in coastal fjords and across the shelf. Coastal waters are compared across two field seasons, with increased freshwater observed during 2014. Horizontal mixing rates of water masses along the WAP ranged from 110–3600 m2 s-1. These mixing rates suggest a rapid transport mechanism for moving meltwater offshore.

Taylor Glacier hosts an active englacial hydrologic system that feeds Blood Falls, a supraglacial outflow of iron-rich subglacial brine at the terminus, despite mean annual air temperatures of −17°C and limited surface melt. Taylor Glacier is an outlet glacier of the East Antarctic ice sheet that terminates in Lake Bonney, McMurdo Dry Valleys. To image and map the brine feeding Blood Falls, we used radio echo sounding to delineate a subhorizontal zone of englacial brine upstream from Blood Falls and elongated in the ice flow direction. We estimate volumetric brine content in excess of 13% within 2 m of the central axis of this zone, and likely much higher at its center. Brine content decreases, but remains detectable, up to 45 m away along some transects. Hence, we infer a network of subparallel basal crevasses allowing injection of pressurized subglacial brine into the ice. Subglacial brine is routed towards Blood Falls by hydraulic potential gradients associated with deeply incised supraglacial valleys. The brine remains liquid within the subglacial and englacial environments through latent heat of freezing coupled with elevated salt content. Our findings suggest that cold glaciers could support freshwater hydrologic systems through localized warming by latent heat alone.

We present glaciochemical data from a pilot study of two snow-pits from Quelccaya ice cap, Peruvian Andes. These are the first samples to be analyzed from Quelccaya for nitrate and sulfate by ion chromatography (IC), for nitrate-plus-nitrite, reactive silicate and reactive iron by colorimetry, and for sodium by atomic absorption spectrophotometry. The 3 m pits used in this study represent a one year record of mass accumulation and the 29 samples collected provide the first glaciochemical data from this area which can be compared with glaciochemical studies from other locations.

Reactive iron, reactive silicate and sodium, and the profiles of >0.63μm microparticles from Thompson and others (1984) are coincident, suggesting that transport and deposition into this area of each species are controlled by similar processes. The common source is probably local, resulting from crustal weathering. In general, the reactive silicate values are lower than those observed in other alpine glacier ice. The highest sulfate and nitrate values were observed in the upper few centimeters of the snow-pit. Most of the sulfate concentrations were less than 3 μM and are similar to values obtained for fresh surface snows from Bolivia (Stallard and Edmond 1981). Since biological gaseous emissions are thought to be the major source of sulfur and nitrogen to the atmosphere over the Amazon basin, the sulfate and nitrate fluctuations may be due to seasonal biological input and/or seasonal shifts in wind direction bringing material to Quelccaya.

With only one exception, the colorimetric nitrate-plus-nitrite data were higher than the IC nitrate data. Unfortunately, the IC analyses were conducted 81 d after the colorimetric analyses. The difference between the two data sets could be attributable to the following: (1) the colorimetric technique may yield erroneously high results as suggested for polar ice by Herron (1982), (2) the IC technique yields erroneously low results due, in part, to the possible exclusion of nitrite concentrations, and/or (3) nitrite was lost via biological removal during the 81 d period before the IC analyses. If the IC data are correct, the mean nitrate value is 0.4μΜ (n = 29). This value is similar to those reported from pre-industrial aged polar ice (Herron 1982). If the colorimetric mean value (1.1 μM) is correct, it is similar to colorimetrically determined values from other high-elevation alpine ice (Lyons and Mayewski 1983).

Since 1979 we have been conducting a program of glaciochemical sampling and analysis in selected portions of the Indian Himalayas. The primary purpose of this work has been the retrieval of data that are of specific use in assessing the signal expressed by the chemistry of air masses entering the Himalayas. The techniques used for this purpose provide data sets for the following: chloride, sodium, reactive iron, reactive silicate, reactive phosphate, nitrite-plus-nitrate, ammonium, pH, oxygen isotopes, deuterium, microparticles, total β-activity, density and scanning electron microscopy. The results of this work appear in a series of papers (Lyons and others 1981, Lyons and Mayewski 1983, Mayewski and others 1981, 1983, 1984 and Goss and others 1985). In summary this work demonstrates: (1) problems encountered in high-altitude ice-core recovery, (2) effects of percolation on chemical records, (3) specific requirements necessary for the retrieval of unaltered glaciochemical records from Himalayan glaciers, (4) potential spatial variability of chemical species concentrations and interpretation of this with respect to time series, (5) usefulness of various glaciochemical indicators as applied to relative dating (seasonality) and air mass tracking, (6) specific details of the chemical and physical properties in Himalayan ice, and (7) recommendations for future Himalayan ice-core studies.

Spectral analysis of time series of a c. 17 ± 0.3 year core, calibrated for total ß activity recovered from Sentik Glacier (4908m) Ladakh, Himalaya, yields several recognizable periodicities including subannual, annual, and multi-annual. The time-series, include both chemical data (chloride, sodium, reactive iron, reactive silicate, reactive phosphate, ammonium, δD, δ(18O) and pH) and physical data (density, debris and ice-band locations, and microparticles in size grades 0.50 to 12.70 μm). Source areas for chemical species investigated and general air-mass circulation defined from chemical and physical time-series are discussed to demonstrate the potential of such studies in the development of paleometeorological data sets from remote high-alpine glacierized sites such as the Himalaya.

The production of climatic-change records using glaciochemical time series has seen minimal application in the Transantarctic Mountains. This is true despite the fact that glacial geologic studies in this area are the primary basis for understanding the glacial history of East Antarctica and thus provide an excellent potential framework for the more detailed records obtainable from glaciochemical studies. Numerous sites within the Transantarctic Mountains fit the requirements necessary for the retrieval of ice cores, and pilot studies have been conducted in both southern Victoria Land (Mayewski and Lyons 1982) and northern Victoria Land (Allen and others 1985). These pilot studies have validated the hypothesis that glaciochemical records retrieved from appropriately chosen ice-core sites in the Transantarctic Mountains can be used for: (1) assessing the current stability of the East Antarctic ice sheet, (2) validating models concerning the recent glacial history of the Transantarctic Mountains, (3) searching for relatively high-frequency (1–100 year) climatic signals, (4) determining changes in the relative geography (ocean – land – ice) of a region, and (5) defining the relative importance of the chemical species source areas (i.e. volcanic, biogenic, anthropogenic, marine, crustal) that provide precipitation to the Transantarctic Mountains.

During the 1984–85 austral summer, a combined University of New Hampshire – Polar Ice Coring Office effort resulted in the recovery of a 201 m long core from a 2800 m high snow massif atop the Dominion Range (85°15'S, 166°10'E), close to the confluence of the Mill and Beardmore glaciers. Chemical and physical data sets to be developed from this ice core, which is estimated to span a period of approximately 1000 years, include: a detailed 6 m snow pit, several shallow snow pits, and fresh and aged surface snow, in combination with a radio echo-sounding survey of the general area, which will be used to provide three-dimensional control. Chemical and physical analyses conducted as part of the study include: stratigraphy, density, sulfate, nitrate, fluoride, chloride, phosphate, sodium, reactive silicate, total beta activity and oxygen isotopes. The oxygen-isotope analyses are being provided by P. Grootes and M. Stuiver (University of Washington), and all other analyses are being conducted by the Glacier Research Group (University of New Hampshire).

In 1984 a 200-m ice core was collected from a local accumulation basin in the Dominion Range, Transantarctic Mountains, Antarctica. A complete oxygen isotope record has been obtained and a considerable portion of the core has been analyzed in detail for chloride, nitrate, sulfate, and sodium. About half of the chloride is due to sea salt with the remainder originating as gaseous HCl. Nitrate levels have increased markedly over the last 1000 years whereas the levels of the other constituents have remained fairly constant.

The oxygen isotope results suggest that this region of Antarctica is responding to long-term global climate forcing as well as to shorter-term climatic variations. This data will be compared with the anion and sodium records in order to determine the effects of climatic forcing on these other records. In particular, nitrate appears to vary in concert with fluctuations in long-term climate. Additionally, variations in each constituent over the 3500 year period will be examined in detail to determine the influence of other processes which affect their concentrations.

Two snow and ice cores from the Rennick Glacier area, Antarctica (study area center point lat 71°15ˈS, long 162°30ˈE) were analyzed for the chemical species: chloride, sodium, reactive silicate, sulfate and nitrate. Core E10 (6.35 m) was taken from Evans Névé, a large accumulation basin at the head of Rennick Glacier. Core M1 (4.35 m) was extracted from the accumulation zone on the central plateau of the Morozumi Range, a small mountain massif bordering Rennick Glacier. Cores E10 and M1 span the time periods from 1929 to 1981 and from 1971 to 1981, respectively, as dated using seasonal variations in chloride (E10) and sulfate (M1) concentrations. An estimated net balance of 50 kg m−2 a−1 was derived for site E10 and of 182 kg m−2 a−1 for site M1. The difference in net mass balance may be explained by elevational differences (M1 1400 m a.s.1., E10 2305 m a.s.1.). Recent (1973 to 1980) increases in sodium, silicate and sulfate at site E10 may be linked to decreases in Antarctic pack-ice extent (Kukla and Gavin 1981) for the same period.

The aim of the study was to determine if soil salt deliquescence and brine hydration can occur under laboratory conditions using natural McMurdo Dry Valleys soils. The experiment was a laboratory analogue for the formation of isolated patches of hypersaline, damp soil, referred to as ‘wet patches’. Soils were oven dried and then hydrated in one of two humidity chambers: one at 100% relative humidity and the second at 75% relative humidity. Soil hydration is highly variable, and over the course of 20 days of hydration, ranged from increases in water content by mass from 0–16% for 122 soil samples from Taylor Valley. The rate and absolute amount of soil hydration correlates well with the soluble salt content of the soils but not with grain size distribution. This suggests that the formation of bulk pore waters in these soils is a consequence of salt deliquescence and hydration of the brine from atmospheric water vapour.

Small changes in the availability of liquid water can have profound effects on the water levels, aqueous chemistry and biogeochemical dynamics of the closed-basin, perennially ice-covered lakes of the McMurdo Dry Valleys, Antarctica. We have compiled the published and unpublished data on dissolved gas, tritium and chlorofluorocarbons (CFCs) for Lake Fryxell and Lake Hoare to determine the effects of a high meltwater year (2001–02 summer) on the lakes. The dissolved gas, tritium and CFC data indicate that the pulse of freshwater that flowed onto the surfaces of the lakes did not mix extensively with the upper water column. At the bottom of Lake Hoare, the measurable CFC and lower dissolved gas values suggest that the recent meltwater may have mixed with bottom waters. The probable mechanism for this transportation is weak density currents with c. 0.1–1.5% surface water being transported downwards in Lake Hoare. This deep water input, while not constant, may have a significant effect on the chemistry of the bottom waters in Lake Hoare over time. In Lake Fryxell, the tritium and CFC data indicate that the recent meltwater did not significantly affect the bottom water chemistry; therefore, weak density currents may not be present in Lake Fryxell.

Water tracks are zones of high soil moisture that route shallow groundwater down-slope, through the active layer and above the ice table. A water track in Taylor Valley, McMurdo Dry Valleys, was analysed for surface hydrogeological, geochemical, and biological characteristics in order to test the hypothesis that water tracks provide spatial structure to Antarctic soil ecosystems by changing the physical conditions in the soil environment within the water tracks from those outside the water tracks. The presence of the water track significantly affected the distribution of biotic and abiotic ecosystem parameters: increasing soil moisture, soil salinity, and soil organic matter within the water track relative to soils outside the water track, and reducing soil phosphate, soil pH, and the population of nematodes and other invertebrates in water track soils relative to off track soils. These results suggest that water tracks are distinct and extreme ecological zones in Taylor Valley that provide long-range (kilometre to multi- kilometre) structure to Antarctic hillslope ecosystems through physical control on soil moisture and solute content. Contrary to expectations, these high soil-moisture sites are not hotspots for faunal biological activity because high soil salinity makes them suitable habitats for only the most halo-tolerant organisms.