Arctic Snowpack Research Articles

Springtime Bromine Activation over Coastal and Inland Arctic Snowpacks

With the return of sunlight in the polar spring, the snowpack serves as an effective source of molecular halogens to the Arctic boundary layer. Reactive bromine production and associated ozone depl...

Mercury in the Arctic tundra snowpack: temporal and spatial concentration patterns and trace gas exchanges

Abstract. In the Arctic, the snowpack forms the major interface between atmospheric and terrestrial cycling of mercury (Hg), a global pollutant. We investigated Hg dynamics in an interior Arctic tundra snowpack in northern Alaska during two winter seasons. Using a snow tower system to monitor Hg trace gas exchange, we observed consistent concentration declines of gaseous elemental Hg (Hggas0) from the atmosphere to the snowpack to soils. The snowpack itself was unlikely a direct sink for atmospheric Hggas0. In addition, there was no evidence of photochemical reduction of HgII to Hggas0 in the tundra snowpack, with the exception of short periods during late winter in the uppermost snow layer. The patterns in this interior Arctic snowpack thus differ substantially from observations in Arctic coastal and temperate snowpacks. We consistently measured low concentrations of both total and dissolved Hg in snowpack throughout the two seasons. Chemical tracers showed that Hg was mainly associated with local mineral dust and regional marine sea spray inputs. Mass balance calculations show that the snowpack represents a small reservoir of Hg, resulting in low inputs during snowmelt. Taken together, the results from this study suggest that interior Arctic snowpacks are negligible sources of Hg to the Arctic.

Molecular Halogens Above the Arctic Snowpack: Emissions, Diurnal Variations, and Recycling Mechanisms

AbstractElevated levels of reactive bromine and chlorine species in the springtime Arctic boundary layer contribute to ozone depletion and mercury oxidation, as well as reactions with volatile organic compounds. Recent laboratory and field studies have revealed that snowpack photochemistry leads to Br2 and Cl2 production, the mechanisms of which remain poorly understood. In this work, we use a photochemical box model, with a simplified snow module, to examine the halogen chemistry occurring during the March 2012 Bromine, Ozone, and Mercury Experiment (BROMEX) near Utqiaġvik (Barrow), Alaska. Elevated daytime Br2 levels (e.g., 6–30 parts per trillion (ppt) at around local noon) reported in previous studies and in this work may be explained by Br + BrNO2/BrONO2 reactions under conditions of depleted O3 (<~10 ppb) and background NO2 (10–100 ppt). Even at low background NOx levels at Utqiaġvik, ClONO2 is predicted to be important in the production of Cl2 via multiphase reaction with Cl−. In the late afternoon, photolysis alone cannot explain the rapid decrease of Cl2 observed in the Arctic boundary layer. Heterogeneous reactions of Cl2 on aerosol particles and surface snowpack are suggested to play a key role in atmospheric Cl2 removal and possible BrCl production. Given the importance of the snowpack in the multiphase chemistry of the Arctic boundary layer, future measurements should focus on vertically resolved measurements of NOx and reactive halogens, as well as simultaneous particulate and snow halide measurements, to further evaluate and isolate the halogen production and vertical propagation mechanisms through one‐dimensional modeling.

Seasonal evolution of the effective thermal conductivity of the snow and the soil in high Arctic herb tundra at Bylot Island, Canada

Abstract. The values of the snow and soil thermal conductivity, ksnow and ksoil, strongly impact the thermal regime of the ground in the Arctic, but very few data are available to test model predictions for these variables. We have monitored ksnow and ksoil using heated needle probes at Bylot Island in the Canadian High Arctic (73° N, 80° W) between July 2013 and July 2015. Few ksnow data were obtained during the 2013–2014 winter, because little snow was present. During the 2014–2015 winter ksnow monitoring at 2, 12 and 22 cm heights and field observations show that a depth hoar layer with ksnow around 0.02 W m−1 K−1 rapidly formed. At 12 and 22 cm, wind slabs with ksnow around 0.2 to 0.3 W m−1 K−1 formed. The monitoring of ksoil at 10 cm depth shows that in thawed soil ksoil was around 0.7 W m−1 K−1, while in frozen soil it was around 1.9 W m−1 K−1. The transition between both values took place within a few days, with faster thawing than freezing and a hysteresis effect evidenced in the thermal conductivity–liquid water content relationship. The fast transitions suggest that the use of a bimodal distribution of ksoil for modelling may be an interesting option that deserves further testing. Simulations of ksnow using the snow physics model Crocus were performed. Contrary to observations, Crocus predicts high ksnow values at the base of the snowpack (0.12–0.27 W m−1 K−1) and low ones in its upper parts (0.02–0.12 W m−1 K−1). We diagnose that this is because Crocus does not describe the large upward water vapour fluxes caused by the temperature gradient in the snow and soil. These fluxes produce mass transfer between the soil and lower snow layers to the upper snow layers and the atmosphere. Finally, we discuss the importance of the structure and properties of the Arctic snowpack on subnivean life, as species such as lemmings live under the snow most of the year and must travel in the lower snow layer in search of food.

Bromide and chloride distribution across the snow‐sea ice‐ocean interface: A comparative study between an Arctic coastal marine site and an experimental sea ice mesocosm

AbstractDuring springtime in the Arctic, bromine explosion events occur when high concentrations of reactive bromine species are observed in the boundary layer with the concurrence of ozone depletion events and mercury depletion events. While a variety of substrates including snow, sea ice, frost flowers, and aerosols have been proposed to be the substrate and/or source of bromine activation in the Arctic, recent studies have highlighted the role of snow. Here we report concentration profiles of halides (Br− and Cl−), Na+, and mercury across the snow‐sea ice‐seawater interface at a coastal marine site in the Canadian Arctic Archipelago in March and June 2014, as well as in an experimental sea ice mesocosm in Winnipeg in January and February 2014. The occurrence of bromine activation at the Arctic site in March was indicated by the high mercury concentrations in snowpack. At both the Arctic and mesocosm sites, the molar ratios of Br−/Na+ were nearly constant throughout the sea ice depth, but highly variable in the upper layer of the overlying snowpack, revealing that bromine activation takes place in the sunlit snow instead of sea ice. This is supported by calculations showing that the loss of Br– from the upper layer of the snowpack is large enough to produce the observed concentrations of reactive bromine in the atmospheric boundary layer. However, the upper layer of the Arctic snowpack tends to be generally enriched in Br– due to the net addition of Br–‐containing gases and nonsea‐salt aerosols.

Pre-Melt Energy Budget of an Arctic Snowpack on Landfast First-Year Sea Ice

ABSTRACTThe pre-melt energy budget of a snowpack on landfast first-year sea ice at a remote site in the Canadian Arctic Archipelago was analyzed. Over a 19-day period, the total heat conducted into the snowpack at the snow–sea-ice interface was the largest single energy transfer to the snowpack, while each of the turbulent heat fluxes removed comparable amounts of energy. The total energy transferred from the snowpack (∑Q ≈ −7027 kJ m−2) should have reduced its temperature; however, the opposite occurred. The snowpack’s temperature at both the 7 and 13 cm depths increased over the pre-melt period. The total change in internal energy and latent heat of the snowpack (ΔUsnowpack), derived from 15-minute changes in the snowpack’s temperature over the pre-melt period, was approximately 672 kJ m−2. Closure of the energy budget was not achieved for either the daily or the total pre-melt period. The terms of the energy budget were determined independently; thus, the failure to close the energy budget was the result of the accumulation of errors associated with all the terms. However, for snow on first-year sea ice, the parameterization of the salinity and temperature dependence of the “specific heat” of the basal layer of the snowpack was likely the primary source of error. The snowpack plays a central role in the transfer of energy across the ocean–sea-ice–atmosphere interface, but an adequate method for modelling the evolution of snow on Arctic sea ice including the energy budget, which determines the warming rate and subsequent melt rate of the snow, has yet to be developed.

Potential drivers of microbial community structure and function in Arctic spring snow.

The Arctic seasonal snowpack can extend at times over a third of the Earth’s land surface. This chemically dynamic environment interacts constantly with different environmental compartments such as atmosphere, soil and meltwater, and thus, strongly influences the entire biosphere. However, the microbial community associated with this habitat remains poorly understood. Our objective was to investigate the functional capacities, diversity and dynamics of the microorganisms in snow and to test the hypothesis that their functional signature reflects the snow environment. We applied a metagenomic approach to nine snow samples taken over 2 months during the spring season. Fungi, Bacteroidetes, and Proteobacteria were predominant in metagenomic datasets and changes in community structure were apparent throughout the field season. Functional data that strongly correlated with chemical parameters like mercury or nitrogen species supported that this variation could be explained by fluctuations in environmental conditions. Through inter-environmental comparisons we examined potential drivers of snowpack microbial community functioning. Known cold adaptations were detected in all compared environments without any apparent differences in their relative abundance, implying that adaptive mechanisms related to environmental factors other than temperature may play a role in defining the snow microbial community. Photochemical reactions and oxidative stress seem to be decisive parameters in structuring microbial communities inside Arctic snowpacks.

Microbial Cell Retention in a Melting High Arctic Snowpack, Svalbard

While elution processes of ions and solutes from alpine and arctic snowpacks are well known, the scientific knowledge of the effects on microbial cells and their link to glacial surface ecology during this period is very limited. Here we show that dissolved substances are eluted from a High Arctic snowpack according to previous reports, while the microbial cells are retained and most likely also proliferate. Their retention enhances the interaction between the snowpack-derived microorganisms and microbial communities living on the surface of glaciers, a habitat known for its cell retention, especially those associated with debris known as cryoconite. Microbial biomass is retained during all stages of the summer ablation upon these Arctic glaciers, emphasizing the need to explore the feedback between microbial growth and meltwater biogeochemistry. Furthermore, the snowpack stratigraphy at Midtre Lovénbreen, Svalbard, shows a frequently low abundance of cells, typically corresponding to those of cloud water. However, a few layers show higher bacterial numbers (up to 104 cells mL−1) that occur with an increase of dust particles and most likely originate from local sources.

Elemental carbon measurements in European Arctic snow packs

AbstractBlack carbon (BC) and other light‐absorbing particles deposited on snow and ice are known to perturb the surface radiative balance. There are few published observations of the concentration of these particles in the snow in Scandinavia and the European Arctic. We measured BC concentrations in snow samples collected in this region from 2007 to 2009, and we present the results here. The data set includes 484 surface samples and 24 column samples (covering the accumulation season) from snow on land, glaciers, and sea ice. Concentrations up to 88 ng of carbon per gram of snow (ng/g) were found in Scandinavia, while lower values were observed at higher latitudes: 11–14 ng/g in Svalbard, 7–42 ng/g in the Fram Strait, and 9 ng/g in Barrow. Values compare well with other observations but are generally found to be a factor of 2–3 higher than modeled BC concentrations in snow in the chemical transport model Oslo CTM2. This model underestimation comes in spite of potentially significant undercatch in the observations. The spring melt period enhanced BC levels in surface snow at the four sites where the BC concentrations were monitored from March to May in 2008 and 2009. A data set of replicate samples is used to establish a concentration‐dependent estimate of the meter‐scale variability of BC concentration in snow, found to be around ±30% of the average concentration.

Interactions between snow chemistry, mercury inputs and microbial population dynamics in an Arctic snowpack.

We investigated the interactions between snowpack chemistry, mercury (Hg) contamination and microbial community structure and function in Arctic snow. Snowpack chemistry (inorganic and organic ions) including mercury (Hg) speciation was studied in samples collected during a two-month field study in a high Arctic site, Svalbard, Norway (79°N). Shifts in microbial community structure were determined by using a 16S rRNA gene phylogenetic microarray. We linked snowpack and meltwater chemistry to changes in microbial community structure by using co-inertia analyses (CIA) and explored changes in community function due to Hg contamination by q-PCR quantification of Hg-resistance genes in metagenomic samples. Based on the CIA, chemical and microbial data were linked (p = 0.006) with bioavailable Hg (BioHg) and methylmercury (MeHg) contributing significantly to the ordination of samples. Mercury was shown to influence community function with increases in merA gene copy numbers at low BioHg levels. Our results show that snowpacks can be considered as dynamic habitats with microbial and chemical components responding rapidly to environmental changes.

Microbial nitrogen cycling in Arctic snowpacks

Arctic snowpacks are often considered as chemical reactors for a variety of chemicals deposited through wet and dry events, but are overlooked as potential sites for microbial metabolism of reactive nitrogen species. The fate of deposited species is critical since warming leads to the transfer of contaminants to snowmelt-fed ecosystems. Here, we examined the role of microorganisms and the potential pathways involved in nitrogen cycling in the snow. Next generation sequencing data were used to follow functional gene abundances and a 16S rRNA (ribosomal ribonucleic acid) gene microarray was used to follow shifts in microbial community structure during a two-month spring-time field study at a high Arctic site, Svalbard, Norway (79° N). We showed that despite the low temperatures and limited water supply, microbial communities inhabiting the snow cover demonstrated dynamic shifts in their functional potential to follow several different pathways of the nitrogen cycle. In addition, microbial specific phylogenetic probes tracked different nitrogen species over time. For example, probes for Roseomonas tracked nitrate concentrations closely and probes for Caulobacter tracked ammonium concentrations after a delay of one week. Nitrogen cycling was also shown to be a dominant process at the base of the snowpack.

Modeling the influence of photochemistry on hydrogen peroxide concentrations in an Arctic snowpack

While laboratory experiments suggest that hydrogen peroxide (HOOH) on polar snow grains should be completely photolyzed during summer, field measurements show a continuous, multiyear record of HOOH in the snowpack. To understand this discrepancy, we apply a snow parcel model to follow HOOH in the snowpack at Summit, Greenland. Taking into account snowfall and variations in actinic flux, we evaluate the impact of three photochemical factors on HOOH preservation: the quantum efficiency of HOOH photodestruction, HOOH recycling through organic compounds, and HOOH photoproduction from snowpack chromophores. We find that 60%–100% of deposited HOOH is preserved in the first year, with less preservation of HOOH deposited during summer, and that the OH produced from HOOH photolysis likely contributes strongly to transforming snowpack bromide and organic compounds. Our findings suggest that photochemistry plays an important role in HOOH loss in snows at Summit and other polar sites, complementing temperature‐dependent physical processes.

Arctic snowpack bromine release

Snow and ice influence the climate and chemistry of the polar atmosphere. Field experiments in Alaska point to the significance of surface snow for polar ozone depletion events.

The dynamic arctic snow pack: an unexplored environment for microbial diversity and activity.

The Arctic environment is undergoing changes due to climate shifts, receiving contaminants from distant sources and experiencing increased human activity. Climate change may alter microbial functioning by increasing growth rates and substrate use due to increased temperature. This may lead to changes of process rates and shifts in the structure of microbial communities. Biodiversity may increase as the Arctic warms and population shifts occur as psychrophilic/psychrotolerant species disappear in favor of more mesophylic ones. In order to predict how ecological processes will evolve as a function of global change, it is essential to identify which populations participate in each process, how they vary physiologically, and how the relative abundance, activity and community structure will change under altered environmental conditions. This review covers aspects of the importance and implication of snowpack in microbial ecology emphasizing the diversity and activity of these critical members of cold zone ecosystems.

Production of gas phase NO2 and halogens from the photolysis of thin water films containing nitrate, chloride and bromide ions at room temperature

Nitrate and halide ions coexist in particles generated in marine regions, around alkaline dry lakes, and in the Arctic snowpack. Although the photochemistry of nitrate ions in bulk aqueous solution is well known, there is recent evidence that it may be more efficient at liquid-gas interfaces, and that the presence of other ions in solution may enhance interfacial reactivity. This study examines the 311 nm photolysis of thin aqueous films of ternary halide-nitrate salt mixtures (NaCl-NaBr-NaNO3) deposited on the walls of a Teflon chamber at 298 K. The films were generated by nebulizing aqueous 0.25 M NaNO3 solutions which had NaCl and NaBr added to vary the mole fraction of halide ions. Molar ratios of chloride to bromide ions were chosen to be 0.25, 1.0, or 4.0. The subsequent generation of gas phase NO2 and reactive halogen gases (Br2, BrCl and Cl2) were monitored with time. The rate of gas phase NO2 formation was shown to be enhanced by the addition of the halide ions to thin films containing only aqueous NaNO3. At [Cl(-)]/[Br(-)] ≤ 1.0, the NO2 enhancement was similar to that observed for binary NaBr-NaNO3 mixtures, while with excess chloride NO2 enhancement was similar to that observed for binary NaCl-NaNO3 mixtures. Molecular dynamics simulations predict that the halide ions draw nitrate ions closer to the interface where a less complete solvent shell allows more efficient escape of NO2 to the gas phase, and that bromide ions are more effective in bringing nitrate ions closer to the surface. The combination of theory and experiments suggests that under atmospheric conditions where nitrate ion photochemistry plays a role, the impact of other species such as halide ions should be taken into account in predicting the impacts of nitrate ion photochemistry.

Carbonaceous species and humic like substances (HULIS) in Arctic snowpack during OASIS field campaign in Barrow

Snowpacks contain many carbonaceous species that can potentially impact on snow albedo and arctic atmospheric chemistry. During the OASIS field campaign, in March and April 2009, Elemental Carbon (EC), Water insoluble Organic Carbon (WinOC) and Dissolved Organic Carbon (DOC) were investigated in various types of snow: precipitating snows, remobilized snows, wind slabs and depth hoars. EC was found to represent less than 5% of the Total Carbon Content (TCC = EC + WinOC + DOC), whereas WinOC was found to represent an unusual 28 to 42% of TCC. Snow type was used to infer physical processes influencing the evolution of different fractions of DOC. DOC is highest in soil influenced indurated depth hoar layers due to specific wind related formation mechanisms in the early season. Apart from this specific snow type, DOC is found to decrease from precipitating snow to remobilized snow to regular depth hoar. This decrease is interpreted as due to cleaving photochemistry and physical equilibration of the most volatile fraction of DOC. Depending on the relative proportions of diamond dust and fresh snow in the deposition of the seasonal snowpack, we estimate that 31 to 76% of DOC deposited to the snowpack is reemitted back to the boundary layer. Under the assumption that this reemission is purely photochemical, we estimate an average flux of VOC out of the snowpack of 20 to 170 μgC m−2 h−1. Humic like substances (HULIS), short chain diacids and aldehydes are quantified, and showed to represent altogether a modest (<20%) proportion of DOC, and less than 10% of DOC + WinOC. HULIS optical properties are measured and could be consistent with aged biomass burning or a possible marine source.

Production of Gas Phase NO2 and Halogens from the Photochemical Oxidation of Aqueous Mixtures of Sea Salt and Nitrate Ions at Room Temperature

Nitrate and halide ions coexist in a number of environmental systems, including sea salt particles, the Arctic snowpack, and alkaline dry lakes. However, little is known about potential synergisms between halide and nitrate ions. The effect of sea salt on NO(3)(-) photochemistry at 311 nm was investigated at 298 K using thin films of deliquesced NaNO(3)-synthetic sea salt mixtures. Gas phase NO(2), NO, and halogen products were measured as a function of photolysis time using NO(y) chemiluminescence and atmospheric pressure ionization mass spectrometry (API-MS). The production of NO(2) increases with the halide-to-nitrate ratio, and is similar to that for mixtures of NaCl with NaNO(3). Gas phase halogen production also increased with the halide-to-nitrate ratio, consistent with NO(3)(-) photolysis yielding OH which oxidizes halide ions in the film. Yields of gas phase halogens and NO were strongly dependent on the acidity of the solution, while that of NO(2) was not. An additional halogen formation mechanism in the dark involving molecular HNO(3) is proposed that may be important in other systems such as reactions on surfaces. These studies show that the yield of Br(2) relative to NO(2) during photolysis of halide-nitrate mixtures could be as high as 35% under some atmospheric conditions.

Hydroxyl radical and NOx production rates, black carbon concentrations and light‐absorbing impurities in snow from field measurements of light penetration and nadir reflectivity of onshore and offshore coastal Alaskan snow

Photolytic production rates of NO, NO2 and OH radicals in snow and the total absorption spectrum due to impurities in snowpack have been calculated for the Ocean‐Atmosphere‐Sea‐Ice‐Snowpack (OASIS) campaign during Spring 2009 at Barrow, Alaska. The photolytic production rate and snowpack absorption cross‐sections were calculated from measurements of snowpack stratigraphy, light penetration depths (e‐folding depths), nadir reflectivity (350–700 nm) and UV broadband atmospheric radiation. Maximum NOx fluxes calculated during the campaign owing to combined nitrate and nitrite photolysis were calculated as 72 nmol m−2 h−1 for the inland snowpack and 44 nmol m−2 h−1 for the snow on sea‐ice and snowpack around the Barrow Arctic Research Center (BARC). Depth‐integrated photochemical production rates of OH radicals were calculated giving maximum OH depth‐integrated production rates of ∼160 nmol m−2 h−1 for the inland snowpack and ∼110–120 nmol m−2 h−1 for the snow around BARC and snow on sea‐ice. Light penetration (e‐folding) depths at a wavelength of 400 nm measured for snowpack in the vicinity of Barrow and snow on sea‐ice are ∼9 cm and 14 cm for snow 15 km inland. Fitting scaled HULIS (HUmic‐LIke Substances) and black carbon absorption cross‐sections to the determined snow impurity absorption cross‐sections show a “humic‐like” component to snowpack absorption, with typical concentrations of 1.2–1.5 μgC g−1. Estimates of black carbon concentrations for the four snowpacks are ∼40 to 70 ng g−1 for the terrestrial Arctic snowpacks and ∼90 ng g−1 for snow on sea‐ice.

An isotopic view on the connection between photolytic emissions of NOx from the Arctic snowpack and its oxidation by reactive halogens

We report on dual isotopic analyses (δ15N and Δ17O) of atmospheric nitrate at daily time‐resolution during the OASIS intensive field campaign at Barrow, Alaska, in March–April 2009. Such measurements allow for the examination of the coupling between snowpack emissions of nitrogen oxides (NOx = NO + NO2) and their involvement in reactive halogen‐mediated chemical reactions in the Arctic atmosphere. The measurements reveal that during the spring, lowδ15N values in atmospheric nitrate, indicative of snowpack emissions of NOx, are almost systematically associated with local oxidation of NOx by reactive halogens such as BrO, as indicated by 17O‐excess measurements (Δ17O). The high time‐resolution data from the intensive field campaign were complemented by weekly aerosol sampling between April 2009 and February 2010. The dual isotopic composition of nitrate (δ15N and Δ17O) obtained throughout this nearly full seasonal cycle is presented and compared to other seasonal‐scale measurements carried out in the Arctic and in non‐polar locations. In particular, the data allow for the investigation of the seasonal variations of reactive halogen chemistry and photochemical snowpack NOx emissions in the Arctic. In addition to the well characterized peak of snowpack NOx emissions during springtime in the Arctic (April to May), the data reveal that photochemical NOx emissions from the snowpack may also occur in other seasons as long as snow is present and there is sufficient UV radiation reaching the Earth's surface.

Formaldehyde in the Alaskan Arctic snowpack: Partitioning and physical processes involved in air-snow exchanges

[1] The snowpack is a photochemically active medium which produces numerous key reactive species involved in the atmospheric chemistry of polar regions. Formaldehyde (HCHO) is one such reactive species produced in the snow, and which can be released to the atmospheric boundary layer. Based on atmospheric and snow measurements, this study investigates the physical processes involved in the HCHO air‐snow exchanges observed during the OASIS 2009 field campaign at Barrow, Alaska. HCHO concentration changes in a fresh diamond dust layer are quantitatively explained by the equilibration of a solid solution of HCHO in ice, through solid‐state diffusion of HCHO within snow crystals. Because diffusion of HCHO in ice is slow, the size of snow crystals is a major variable in the kinetics of exchange and the knowledge of the snow specific surface area is therefore crucial. Air‐snow exchanges of HCHO can thus be explained without having to consider processes taking place in the quasi‐liquid layer present at the surface of ice crystals. A flux of HCHO to the atmosphere was observed simultaneously with an increase of HCHO concentration in snow, indicating photochemical production in surface snow. This study also suggests that the difference in bromine chemistry between Alert (Canadian Arctic) and Barrow leads to different snow composition and post‐deposition evolutions. The highly active bromine chemistry at Barrow probably leads to low HCHO concentrations at the altitude where diamond dust formed. Precipitated diamond dust was subsequently undersaturated with respect to thermodynamic equilibrium, which contrasts to what was observed elsewhere in previous studies.