Svalbard Ice Cores Research Articles

Climate change is rapidly deteriorating the climatic signal in Svalbard glaciers

Abstract. The Svalbard archipelago is particularly sensitive to climate change due to the relatively low altitude of its main ice fields and its geographical location in the higher North Atlantic, where the effect of Arctic amplification is more significant. The largest temperature increases have been observed during winter, but increasing summer temperatures, above the melting point, have led to increased glacier melt. Here, we evaluate the impact of this increased melt on the preservation of the oxygen isotope (δ18O) signal in firn records. δ18O is commonly used as a proxy for past atmospheric temperature reconstructions, and, when preserved, it is a crucial parameter to date and align ice cores. By comparing four different firn cores collected in 2012, 2015, 2017 and 2019 at the top of the Holtedahlfonna ice field (1100 m a.s.l.), we show a progressive deterioration of the isotope signal, and we link its degradation to the increased occurrence and intensity of melt events. Our findings indicate that, starting from 2015, there has been an escalation in melting and percolation resulting from changes in the overall atmospheric conditions. This has led to the deterioration of the climate signal preserved within the firn or ice. Our observations correspond with the model's calculations, demonstrating an increase in water percolation since 2014, potentially reaching deeper layers of the firn. Although the δ18O signal still reflects the interannual temperature trend, more frequent melting events may in the future affect the interpretation of the isotopic signal, compromising the use of Svalbard ice cores. Our findings highlight the impact and the speed at which Arctic amplification is affecting Svalbard's cryosphere.

Organic Compounds, Radiocarbon, Trace Elements and Atmospheric Transport Illuminating Sources of Elemental Carbon in a 300‐Year Svalbard Ice Core

AbstractBlack carbon (BC) particles produced by incomplete combustion of biomass and fossil fuels warm the atmosphere and decrease the reflectivity of snow and ice, hastening their melt. Although the significance of BC in Arctic climate change is widely acknowledged, observations on its deposition and sources are few. We present BC source types in a 300‐year (1700–2005) Svalbard ice core by analysis of particle‐bound organic compounds, radiocarbon, and trace elements. According to the radiocarbon results, 58% of the deposited elemental carbon (EC, thermal‐optical proxy of BC) is of non‐fossil origin throughout the record, while the organic compounds suggest a higher percentage (68%). The contribution of fossil fuels to EC is suggested to have been elevated between 1860 and 1920, particularly based on the organics and trace element data. A second increase in fossil fuel sources seems to have occurred near the end of the record: according to radiocarbon measurements between 1960 and 1990, while the organics and trace element data suggest that the contribution of fossil fuels has increased since the 1970s to the end of the record, along with observed increasing EC deposition. Modeled atmospheric transport between 1948 and 2004 shows that increasing EC deposition observed at the glacier during that period can be associated with increased atmospheric transport from Far East Asia. Further observational BC source data are essential to help target climate change mitigation efforts. The combination of robust radiocarbon with organic compound analyses requiring low sample amounts seems a promising approach for comprehensive Arctic BC source apportionment.

Levels and distribution profiles of Per- and Polyfluoroalkyl Substances (PFAS) in a high Arctic Svalbard ice core

Per- and polyfluoroalkyl substances (PFAS) are a group of persistent organic contaminants of which some are toxic and bioaccumulative. Several PFAS can be formed from the atmospheric degradation of precursors such as fluorotelomer alcohols (FTOHs) as well as hydrochlorofluorocarbons (HFCs) and other ozone-depleting chlorofluorocarbon (CFC) replacement compounds. Svalbard ice cores have been shown to provide a valuable record of long-range atmospheric transport of contaminants to the Arctic. This study uses a 12.3 m ice core from the remote Lomonosovfonna ice cap on Svalbard to understand the atmospheric deposition of PFAS in the Arctic. A total of 45 PFAS were targeted, of which 26 were detected, using supercritical fluid chromatography (SFC) tandem mass spectrometry (MS/MS) and ultra-performance liquid chromatography (UPLC) MS/MS. C2 to C11 perfluoroalkyl carboxylic acids (PFCAs) were detected continuously in the ice core and their fluxes ranged from 2.5 to 8200 ng m−2 yr−1 (9.51–16,500 pg L−1). Trifluoroacetic acid (TFA) represented 71 % of the total mass of C2 – C11 PFCAs in the ice core and had increasing temporal trends in deposition. The distribution profile of PFCAs suggested that FTOHs were likely the atmospheric precursor to C8 – C11 PFCAs, whereas C2 – C6 PFCAs had alternative sources, such as HFCs and other CFC replacement compounds. Perfluorooctanesulfonic acid (PFOS) was also widely detected in 82 % of ice core subsections, and its isomer profile (81 % linear) indicated an electrochemical fluorination manufacturing source. Comparisons of PFAS concentrations with a marine aerosol proxy showed that marine aerosols were insignificant for the deposition of PFAS on Lomonosovfonna. Comparisons with a melt proxy showed that TFA and PFOS were mobile during meltwater percolation. This indicates that seasonal snowmelt and runoff from post-industrial accumulation on glaciers could be a significant seasonal source of PFAS to ecosystems in Arctic fjords.

Ice core records of levoglucosan and dehydroabietic and vanillic acids from Aurora Peak in Alaska since the 1660s: a proxy signal of biomass-burning activities in the North Pacific Rim

Abstract. A 180 m long (343 years) ice core was drilled in the saddle of Aurora Peak in Alaska (63.52∘ N, 146.54∘ W; elevation: 2825 m) and studied for biomass-burning tracers. Concentrations of levoglucosan and dehydroabietic and vanillic acids exhibit multidecadal variability, with higher spikes in 1678, 1692, 1695, 1716, 1750, 1764, 1756, 1834, 1898, 1913, 1966 and 2005 CE. Historical trends of these compounds showed enhanced biomass-burning activities in the deciduous broadleaf forests, boreal conifer forests, and/or tundra woodland and mountain ecosystems before the 1830s and after the Great Pacific Climate Shift (GPCS). The gradually elevated level of dehydroabietic acid after the GPCS is similar to p-hydroxybenzoic acid (p-HBA) from the Svalbard ice core, suggesting common climate variability in the Northern Hemisphere. The periodic cycle of levoglucosan, which seemed to be associated with the Pacific Decadal Oscillation (PDO), may be more involved with the long-range atmospheric transport than other species. These compounds showed significant correlations with global lower-tropospheric temperature anomalies (GLTTAs). The relations of the biomass-burning tracers with the PDO and GLTTA in this study suggest that their emission, frequency and deposition are controlled by the climate-driven forces. In addition, historical trends of dehydroabietic and vanillic acids (burning products of resin and lignin, respectively) from our ice core demonstrate the Northern Hemispheric connections to the common source regions as suggested from other ice core studies from Svalbard, Akademii Nauk and Tunu Greenland in the Northern Hemisphere.

Do contemporary (1980–2015) emissions determine the elemental carbon deposition trend at Holtedahlfonna glacier, Svalbard?

Abstract. The climate impact of black carbon (BC) is notably amplified in the Arctic by its deposition, which causes albedo decrease and subsequent earlier snow and ice spring melt. To comprehensively assess the climate impact of BC in the Arctic, information on both atmospheric BC concentrations and deposition is essential. Currently, Arctic BC deposition data are very scarce, while atmospheric BC concentrations have been shown to generally decrease since the 1990s. However, a 300-year Svalbard ice core showed a distinct increase in EC (elemental carbon, proxy for BC) deposition from 1970 to 2004 contradicting atmospheric measurements and modelling studies. Here, our objective was to decipher whether this increase has continued in the 21st century and to investigate the drivers of the observed EC deposition trends. For this, a shallow firn core was collected from the same Svalbard glacier, and a regional-to-meso-scale chemical transport model (SILAM) was run from 1980 to 2015. The ice and firn core data indicate peaking EC deposition values at the end of the 1990s and lower values thereafter. The modelled BC deposition results generally support the observed glacier EC variations. However, the ice and firn core results clearly deviate from both measured and modelled atmospheric BC concentration trends, and the modelled BC deposition trend shows variations seemingly independent from BC emission or atmospheric BC concentration trends. Furthermore, according to the model ca. 99 % BC mass is wet-deposited at this Svalbard glacier, indicating that meteorological processes such as precipitation and scavenging efficiency have most likely a stronger influence on the BC deposition trend than BC emission or atmospheric concentration trends. BC emission source sectors contribute differently to the modelled atmospheric BC concentrations and BC deposition, which further supports our conclusion that different processes affect atmospheric BC concentration and deposition trends. Consequently, Arctic BC deposition trends should not directly be inferred based on atmospheric BC measurements, and more observational BC deposition data are required to assess the climate impact of BC in Arctic snow.

Taxonomic characterization and the bio-potential of bacteria isolated from glacier ice cores in the High Arctic.

Glacier ice and firn cores have ecological and biotechnological importance. The present study is aimed at characterizing bacteria in crustal ice cores from Svalbard, the Arctic. Counts of viable isolates ranged from 10 to 7000 CFU/ml (mean 803 CFU/ml) while the total bacterial numbers ranged from 7.20 × 10(4) to 2.59 × 10(7) cells ml(-1) (mean 3.12 × 10(6) cells ml(-1) ). Based on 16S rDNA sequence data, the identified species belonged to seven species, namely Bacillus barbaricus, Pseudomonas orientalis, Pseudomonas oryzihabitans, Pseudomonas fluorescens, Pseudomonas syncyanea, Sphingomonas dokdonensis, and Sphingomonas phyllosphaerae, with a sequence similarity ranging between 93.5 and 99.9% with taxa present in the database. The isolates exhibited unique phenotypic properties, and three isolates (MLB-2, MLB-5, and MLB-9) are novel species, yet to be described. To the best of our knowledge, this is the first report on characterization of cultured bacterial communities from Svalbard ice cores. We conclude that high lipase, protease, cellulase, amylase, and urease activities expressed by most of the isolates provide a clue to the potential industrial applications of these organisms. These microbes, producing cold-adapted enzymes may provide an opportunity for biotechnological research.

Increase in elemental carbon values between 1970 and 2004 observed in a 300-year ice core from Holtedahlfonna (Svalbard)

Abstract. Black carbon (BC) is a light-absorbing particle that warms the atmosphere–Earth system. The climate effects of BC are amplified in the Arctic, where its deposition on light surfaces decreases the albedo and causes earlier melt of snow and ice. Despite its suggested significant role in Arctic climate warming, there is little information on BC concentrations and deposition in the past. Here we present results on BC (here operationally defined as elemental carbon (EC)) concentrations and deposition on a Svalbard glacier between 1700 and 2004. The inner part of a 125 m deep ice core from Holtedahlfonna glacier (79°8' N, 13°16' E, 1150 m a.s.l.) was melted, filtered through a quartz fibre filter and analysed for EC using a thermal–optical method. The EC values started to increase after 1850 and peaked around 1910, similar to ice core records from Greenland. Strikingly, the EC values again increase rapidly between 1970 and 2004 after a temporary low point around 1970, reaching unprecedented values in the 1990s. This rise is not seen in Greenland ice cores, and it seems to contradict atmospheric BC measurements indicating generally decreasing atmospheric BC concentrations since 1989 in the Arctic. For example, changes in scavenging efficiencies, post-depositional processes and differences in the vertical distribution of BC in the atmosphere are discussed for the differences between the Svalbard and Greenland ice core records, as well as the ice core and atmospheric measurements in Svalbard. In addition, the divergent BC trends between Greenland and Svalbard ice cores may be caused by differences in the analytical methods used, including the operational definitions of quantified particles, and detection efficiencies of different-sized BC particles. Regardless of the cause of the increasing EC values between 1970 and 2004, the results have significant implications for the past radiative energy balance at the coring site.

Nitrate and Sulfate Anthropogenic Trends in the 20th Century from Five Svalbard Ice Cores

Sulfate and nitrate records from 5 ice cores spread across Svalbard were compared and revealed strong temporal similarities with previously published global estimates of SO2 and NOx anthropogenic emissions during the 20th century. A significant departure from the early century sulfate and nitrate levels was evident at all drilling sites starting from the mid-1940s. A steady increase was observed in both sulfate and nitrate profiles at most sites until the late 1960s, when the annual concentrations started to increase at a higher rate. This peak activity lasted for about a decade, and was observed to decrease steadily from the early 1980s on, when sulfate levels declined significantly and when nitrate levels finally reached sulfate levels for the first time in 20th century. The timing of these trends in Svalbard with global SO2 and NOx concentration profiles was best appraised when considering composite concentration profiles of all Svalbard ice cores for sulfate and nitrate, respectively. Composite profiles were also found to provide a convenient mean for distinguishing between the most important world source regions. Based on correlation analysis, the major pollutant sources appeared to be Western Europe and North America for both sulfate and nitrate, followed by Central Europe and former U.S.S.R. in generally similar proportions.

A 150-year Record of Heavy Metals in the Varved Sediments of Lake Bolterskardet, Svalbard

Laminated sediments from Bolterskardet Lake on Svalbard provide a new 150-year record of heavy metals in the Arctic. Independent data of 137Cs and 210Pb indicate that these laminations are annually deposited varves. The high sedimentation rate and varved sediments make Lake Bolterskardet a good site for studying history of heavy metal pollution in the region. A suite of heavy metals (Pb, As, Cd , Cu, Cr, Co, Ni, and Sn) were studied. The variations of Cu, Cr, Co, and Ni concentrations show an inverse pattern with the median grain size. It suggests that the particle size has a significant role in the accumulation and enrichment of heavy metals in the sediments. In the concentration profiles of studied heavy metals, only Pb concentrations show a significant increase from the lower parts to the upper parts of the core. Profiles of “total,” “lithogenic,” and “anthropogenic” Pb flux also show an increasing pattern. Anthropogenic Pb flux varies between 0.1 μg cm−2 yr−1 and 12.3 μg cm−2 yr−1, with a mean value of 2.4 μg cm−2 yr−1. The anthropogenic Pb fluxes were relatively low at around 0.7 μg cm−2 yr−1 prior to 1945, slowly increased after 1945, and reached a sidestep (between 1940s and 1970s) with mean value of 1.8 μg cm−2 yr−1. Second high value period was between 1980s and 1990s with mean value of 5.9 μg cm−2 yr−1. The variation of anthropogenic Pb fluxes before 1970 in Bolterskardet Lake coincides with the sulfate record and Pb concentration data from Greenland snow and ice, and the acidity concentration in the Svalbard ice cores. However, the anthropogenic Pb fluxes during the last two decades show a rapidly increasing trend. This regional pattern may suggest that local source is an important factor for heavy metal contamination in Svalbard, and the complex of long-range transport contaminations for regional and global process.

Two ice-core δ18O records from Svalbard illustrating climate and sea-ice variability over the last 400 years

Ice cores from the relatively low-lying ice caps in Svalbard have not been widely exploited in climatic studies owing to uncertainties about the effect of meltwater percolation. However, results from two new Svalbard ice cores, at Lomonosovfonna and Austfonna, have shown that with careful site selection, high-resolution sampling and multiple chemical analyses it is possible to recover ice cores from which part of the annual signals are preserved, despite the considerable meltwater percolation. The new Svalbard ice cores are positioned in different parts of Svalbard and cover the past 800 years. In this paper we focus on the last 400 years. The 6180 signals from the cores are qualitatively similar over most of the twentieth century, suggesting that they record the same atmospheric signal. Prior to AD 1920, the Austfonna ice core exhibits more negative 6180 values than Lomonosovfonna, although there are intermittent decadal-scale periods throughout the record with similar values. We suggest that the differences reflect the effect of the inversion layer during the winter. The pattern in the 6180 records is similar to the Longyearbyen airtemperature record, but on an annual level the correlation is low. The Austfonna record correlates well with the temperature record from the more distant and southwesterly located Jan Mayen. A comparison of the ice-core and sea-ice records from this period suggests that sea-ice extent and Austfonna 6180 are related over the past 400 years. This may reflect the position of the storm tracks and their direct influence on the relatively low-altitude Austfonna. Lomonosovfonna may be less sensitive to such changes and primarily record free atmospheric changes instead of variations in sea-ice extent, the latter is probably a result of its higher elevation.

Climate oscillations as recorded in svalbard ice core ω18o records between ad 1200 and 1997

ABSTRACT. We apply two different time series analytical tools to ω18O records from two Svalbard ice cores. One ice core is from Lomonosovfonna at 1250 ma.s.l. and the other from Austfonna at 750 m a.s.l. These cores are estimated to cover at least the past 800 years and have been dated using a combination of known reference horizons and glacial modelling. Wavelet analysis reveals low frequency oscillations on the 60–120–year scale on the lower elevation site Austfonna while the higher altitude site on Lomonosovfonna does not reveal such variability throughout the record. The second method, Significant Zero Crossing of Derivates (SiZer) does not resolve the low‐frequency periodicity seen in the wavelet analysis. The low‐frequency variability resolved by the wavelet analysis is similar to what has been found in various climate records including instrumental temperatures and tree‐rings, and has been proposed as the most important oscillation for the observed trends in Arctic air temperatures.

The methanesulfonic acid (MSA) record in a Svalbard ice core

AbstractSvalbard ice cores have not yet been fully exploited for studies of climate and environmental conditions. In one recently drilled ice core from Lomonosovfonna, we have studied the methanesulfonic acid (MSA) records in relation to temperature and sea ice. Under the present climatic conditions, MSA appears to be negatively correlated with the sea-ice conditions in the Barents Sea, and positively correlated with the instrumental temperature record from Svalbard. However, prior to about 1920 the MSA concentrations were about twice as high, despite the more extensive sea-ice coverage. After exploring different possibilities, we suggest that MSA concentrations were higher in the 19th century than in the 20th century due to increased primary production, in response to increased vertical stability of the sea surface layers, caused by increased meltwater production from the more extensive sea-ice cover. Thus, the MSA record from Lomonosovfonna probably both is a measure of the regional sea-ice variability on the multi-decadal scale and reflects locally favorable conditions for marine biogenic dimethyl sulfide (DMS) production on the sub-decadal scale.

Ice cores from Svalbard––useful archives of past climate and pollution history

Ice cores from the relatively low-lying ice caps in Svalbard have not been widely exploited in climatic and environmental studies due to uncertainties about the effect of melt water percolation. However, results from two recent Svalbard ice cores, at Lomonosovfonna (1250 m asl) and Austfonna (750 m asl), have shown that with careful site selection, high-resolution sampling and multiple chemical analyses, it is possible to recover ice cores with partly preserved annual signals. These cores are estimated to cover at least the past 600 years and have been dated using a combination of known reference horizons and glacial modeling. The δ 18O data from both Lomonosovfonna and Austfonna ice cores suggest that the 20th century was the warmest during the past 600 years. A comparison of the ice core and sea ice records from this period suggests that sea ice extent and Austfonna δ 18O are linked over the past 400 years. This may reflect the position of the storm tracks and their direct influence on the relatively low altitude Austfonna. Lomonosovfonna may be less sensitive to such changes and primarily record atmospheric changes due to its higher elevation. The anthropogenic influence on Svalbard environment is illustrated by increased levels of non-sea-salt sulphate, nitrate, acidity, fly-ash and organic contaminants particularly during the second half of 1900s. Decreased concentrations of some components in recent decades most likely reflect emission and use restrictions. However, some current-use organic pesticide compounds show growing concentrations in near surface layers.

Methanesulfonic acid in a Svalbard Ice Core as an indicator of ocean climate

Methanesulfonic acid (MSA) is an atmospheric oxidation product of dimethyl sulfide, produced by marine biota. MSA preserved in a Svalbard glacier between 1920 and 1996 is compared with the sea surface temperature (SST) and sea‐ice extent of the surrounding ocean over the same period. On decadal timescales high MSA concentrations are found to be associated with warm SST and reduced sea‐ice extent. MSA appears to be influenced by climatic changes related to variations in the import of warm Atlantic Water to the Barents Sea. Atlantic Water plays an important role in the Arctic climate system, therefore MSA concentrations may indirectly reflect larger‐scale changes in the region and may be useful as a proxy for past climate.