Glaciers draining to the Hornsund basin (southern Spitsbergen, Svalbard) have experienced a significant retreat and mass volume loss over the last decades, increasing the input of freshwater into the fjord. An increase in freshwater input can influence fjord hydrology, hydrodynamics, sediment flux and biota, especially in a changing climate. Here, we describe the sources of freshwater supply to the fjord based on glaciological and meteorological data from the period 2006 to 2015. The average freshwater input from land to the Hornsund bay is calculated as 2517 ± 82 Mt a −1 , with main contributions from glacier meltwater runoff (986 Mt a −1 ; 39%) and frontal ablation of tidewater glaciers (634 Mt a −1 ; 25%). Tidewater glaciers in Hornsund lose ca. 40% of their mass by frontal ablation. The terminus retreat component accounts for ca. 30% of the mass loss by frontal ablation, but it can vary between 17% and 44% depending on oceanological, meteorological and geomorphological factors. The contribution of the total precipitation over land excluding winter snowfall (520 Mt a −1), total precipitation over the fjord area (180 Mt a −1) and melting of the snow cover over unglaciated areas (197 Mt a −1) to the total freshwater input appear to be small: 21%, 7% and 8%, respectively.

Rapid Arctic warming results in increased winter rain frequencies, which may impact glacial systems. In this paper, we discuss climatology and precipitation form trends, followed by examining the influence of winter rainfall (Oct‒May) on both the mass balance and dynamics of Hansbreen (Svalbard). We used data from the Hornsund meteorological station (01003 WMO), in addition to the original meteorological and glaciological data from three measurement points on Hansbreen. Precipitation phases were identified based on records of weather phenomena and used—along with information on lapse rate—to estimate the occurrence and altitudinal extent of winter rainfall over the glacier. We found an increase in the frequency of winter rain in Hornsund, and that these events impact both glacier mass balance and glacier dynamics. However, the latter varied depending on the degree of snow cover and drainage systems development. In early winter, given the initial, thin snow cover and an inefficient drainage system, rainfall increased glacier velocity. Full-season winter rainfall on well-developed snow was effectively stored in the glacier, contributing on average to 9% of the winter accumulation.

Metals and metalloids in snow on glaciers, depending on the season of deposition, may come from various sources: local rock dust (erosion of the geological substratum), marine aerosol, local human activity (e.g., impurities in combusted fuel and waste incineration), and long-range atmospheric transport. Hansbreen, a glacier located close to the Polish Polar Station in southern Svalbard, is a perfect site to study metals and metalloids: it has a complex geological substratum, has a year-round presence of a small group of people, and is near the coast. We analyzed a snapshot of metal and metalloid concentrations in snow samples from shallow cores corresponding to autumn, winter, and spring deposition on Hansbreen. Eighteen cores of snow were collected across the glacier, revealing the influence of potential local sources of metals and metalloids. In these samples, we predominantly found Na, Mg, and K, followed by Zn, Ca, Al, and Fe. Heavy metals, such as Bi or Hg, were also detected. Cluster analysis of the determined elemental concentrations divided them into three distinct groups: Group 1: Ag, As, Bi, Cd, Hg, Mo, Sb, Se, and Zn—the most diverse cluster, representing mostly long-range transported volatile elements, with possible extra local geological sources; Group 2: Al, Fe, Cu, and Mn—elements with crustal sources; and Group 3: Na, Ca, Mg, K, and Sr—with the main source in sea spray aerosol. The latter interpretation was confirmed by the calculation of sea salt contribution based on the composition of mean seawater and the positive significant correlation between their concentrations and the electrical conductivity of snow samples. In the study site, snow was up to six times more efficient in bringing metal pollution into terrestrial environment, when compared to rain.

Abstract. The Svalbard archipelago, located at the Arctic sea-ice edge between 74 and 81∘ N, is ∼60 % covered by glaciers. The region experiences rapid variations in atmospheric flow during the snow season (from late September to May) and can be affected by air advected from both lower and higher latitudes, which likely impact the chemical composition of snowfall. While long-term changes in Svalbard snow chemistry have been documented in ice cores drilled from two high-elevation glaciers, the spatial variability of the snowpack composition across Svalbard is comparatively poorly understood. Here, we report the results of the most comprehensive seasonal snow chemistry survey to date, carried out in April 2016 across 22 sites on seven glaciers across the archipelago. At each glacier, three snowpits were sampled along the altitudinal profiles and the collected samples were analysed for major ions (Ca2+, K+, Na+, Mg2+, NH4+, SO42-, Br−, Cl−, and NO3-) and stable water isotopes (δ18O, δ2H). The main aims were to investigate the natural and anthropogenic processes influencing the snowpack and to better understand the influence of atmospheric aerosol transport and deposition patterns on the snow chemical composition. The snow deposited in the southern region of Svalbard is characterized by the highest total ionic loads, mainly attributed to sea-salt particles. Both NO3- and NH4+ in the seasonal snowpack reflect secondary aerosol formation and post-depositional changes, resulting in very different spatial deposition patterns: NO3- has its highest loading in north-western Spitsbergen and NH4+ in the south-west. The Br− enrichment in snow is highest in north-eastern glacier sites closest to areas of extensive sea-ice coverage. Spatial correlation patterns between Na+ and δ18O suggest that the influence of long-range transport of aerosols on snow chemistry is proportionally greater above 600–700 m a.s.l.

Abstract. The Svalbard archipelago, between 74° and 81° N, is ∼60 % covered by glaciers and located at the Arctic sea ice edge. The region experiences rapid variations in atmospheric flow during the snow season (from late September to May) and can be affected by air advected both from lower and higher latitudes, which likely impact the chemical composition of snowfall. While long-term changes in Svalbard snow chemistry have been documented in ice cores drilled from two high-elevation glaciers, the spatial variability of the snowpack composition across Svalbard is comparatively poorly understood. Here, we report the results of the most comprehensive seasonal snow chemistry survey to date, carried out in April 2016 across 22 sites on 7 glaciers across the archipelago. At each glacier, three snow pits were sampled along altitudinal profiles and the collected samples were analysed for major ions (Ca2+, K+, Na+, Mg2+, NH+4, SO42−, Br−, Cl− and NO3−) and stable water isotopes (δ18O, δ2H). The main aims were to investigate the natural and anthropogenic processes influencing the snowpack and to better understand the influence of atmospheric aerosol transport and deposition patterns on the snow chemical composition. The snow deposited in the southern region of Svalbard was characterized by the highest total ionic loads, mainly attributed to sea salt particles. Both NO3− and NH4+ in the seasonal snowpack reflected secondary aerosol formation and post-depositional changes, resulting in very different spatial deposition patterns: NO3− had its highest loading in northwestern Spitsbergen, and NH4+ in the southwest. The Br− enrichment in snow was highest in northeastern glacier sites closest to areas of extensive sea ice coverage. Spatial correlation patterns between Na+ and δ18O suggest that the influence of long-range transport of aerosols on snow chemistry is proportionally greater above 600–700 m a.s.l.