scholarly journals Atmospheric composition in the European Arctic and 30 years of the Zeppelin Observatory, Ny-Ålesund

2021 ◽  
Author(s):  
Stephen M. Platt ◽  
Øystein Hov ◽  
Torunn Berg ◽  
Knut Breivik ◽  
Sabine Eckhardt ◽  
...  
Keyword(s):  
Atmospheric Transport ◽  
Monitoring And Evaluation ◽  
High Arctic ◽  
Atmospheric Composition ◽  
The Arctic ◽  
Observation System ◽  
Research Station ◽  
Svalbard Archipelago ◽  
European Arctic ◽  
Norwegian Polar Institute

Abstract. The Zeppelin Observatory (78.90° N, 11.88° E) is located on the Zeppelin Mountain at 472 m above sea level on Spitsbergen, the largest island of the Svalbard archipelago. Established in 1989, the observatory is part of the “Ny-Ålesund Research Station” and an important atmospheric measurement site, one of only a few in the high Arctic and as a part of several European and global monitoring programs and research infrastructures, notably the European Monitoring and Evaluation Programme (EMEP), the Arctic Monitoring and Assessment Programme (AMAP), the Global Atmosphere Watch (GAW), the Aerosols, Clouds, and Trace gases Research InfraStructure (ACTRIS), the Advanced Global Atmospheric Gases Experiment (AGAGE) network, and the Integrated Carbon Observation System (ICOS). The observatory is jointly operated by the Norwegian Polar Institute (NPI), Stockholm University and the Norwegian Institute for Air Research (NILU). Here we detail the establishment of the Zeppelin Observatory including historical measurements of atmospheric composition in the European Arctic leading to its construction. We present a history of the measurements at the observatory and review the current state of the European Arctic atmosphere, including results from trends in greenhouse gases, chlorofluorocarbons (CFCs) and hydrochlorofluorocarbons (HCFCs), other traces gases, persistent organic pollutants (POPs) and heavy metals, aerosols and Arctic haze, and atmospheric transport phenomena.

scholarly journals A trajectory analysis of atmospheric transport of black carbon aerosols to Canadian High Arctic in winter and spring (1990–2005)

2010 ◽  
Vol 10 (2) ◽  
pp. 2221-2244 ◽  
Author(s):  
L. Huang ◽  
S. L. Gong ◽  
S. Sharma ◽  
D. Lavoué ◽  
C. Q. Jia
Keyword(s):  
Regression Model ◽  
Black Carbon ◽  
North American ◽  
Emission Intensity ◽  
Atmospheric Transport ◽  
High Arctic ◽  
The Arctic ◽  
Canadian High Arctic ◽  
Near Surface ◽  
Annual Variations

Abstract. Black carbon (BC) particles accumulated in the Arctic troposphere and deposited over snow have significant effects on radiative forcing of the Arctic regional climate. Applying cluster analysis technique on 10-day backward trajectories, transport pathways affecting Alert (82.5° N, 62.5° W), Nunavut in Canada are identified in this work, along with the associated transport frequency. Based on the atmospheric transport frequency and the estimated BC emission intensity from surrounding regions, a linear regression model is constructed to investigate the inter-annual variations of BC observed at Alert in January and April, representative of winter and spring respectively, between 1990 and 2005. Strong correlations are found between BC concentrations predicted with the regression model and measured at Alert for both seasons (R2 equals 0.77 and 0.81 for winter and spring, respectively). Results imply that atmospheric transport and BC emission are the major contributors to the inter-annual variations in BC concentrations observed at Alert in the cold seasons for the 16-year period. Based on the regression model the relative contributions of regional BC emissions affecting Alert are attributed to the Eurasian sector, composed of the European Union and the former USSR, and the North American sector. Considering both seasons, the model suggests that Eurasia is the major contributor to the near-surface BC levels at the Canadian High Arctic site with an average contribution of over 85% during the 16-year period. In winter, the atmospheric transport of BC aerosols from Eurasia is found to be even more predominant with a multi-year average of 94%. The model estimates smaller contribution from the Eurasian sector in spring (70%) than that in winter. It is also found that the change in Eurasian contributions depends mainly on the reduction of emission intensity, while the changes in both emission and atmospheric transport contributed to the inter-annual variation of North American contributions.

scholarly journals Characterization of transport regimes and the polar dome during Arctic spring and summer using in situ aircraft measurements

2019 ◽  
Vol 19 (23) ◽  
pp. 15049-15071
Author(s):  
Heiko Bozem ◽  
Peter Hoor ◽  
Daniel Kunkel ◽  
Franziska Köllner ◽  
Johannes Schneider ◽  
...  
Keyword(s):  
Potential Temperature ◽  
Lower Troposphere ◽  
High Arctic ◽  
Atmospheric Composition ◽  
The Arctic ◽  
Trace Gas ◽  
Chemical Compositions ◽  
Second Phase ◽  
Air Masses ◽  
Mixing Ratios

Abstract. The springtime composition of the Arctic lower troposphere is to a large extent controlled by the transport of midlatitude air masses into the Arctic. In contrast, precipitation and natural sources play the most important role during summer. Within the Arctic region sloping isentropes create a barrier to horizontal transport, known as the polar dome. The polar dome varies in space and time and exhibits a strong influence on the transport of air masses from midlatitudes, enhancing transport during winter and inhibiting transport during summer. We analyzed aircraft-based trace gas measurements in the Arctic from two NETCARE airborne field campaigns (July 2014 and April 2015) with the Alfred Wegener Institute Polar 6 aircraft, covering an area from Spitsbergen to Alaska (134 to 17∘ W and 68 to 83∘ N). Using these data we characterized the transport regimes of midlatitude air masses traveling to the high Arctic based on CO and CO2 measurements as well as kinematic 10 d back trajectories. We found that dynamical isolation of the high Arctic lower troposphere leads to gradients of chemical tracers reflecting different local chemical lifetimes, sources, and sinks. In particular, gradients of CO and CO2 allowed for a trace-gas-based definition of the polar dome boundary for the two measurement periods, which showed pronounced seasonal differences. Rather than a sharp boundary, we derived a transition zone from both campaigns. In July 2014 the polar dome boundary was at 73.5∘ N latitude and 299–303.5 K potential temperature. During April 2015 the polar dome boundary was on average located at 66–68.5∘ N and 283.5–287.5 K. Tracer–tracer scatter plots confirm different air mass properties inside and outside the polar dome in both spring and summer. Further, we explored the processes controlling the recent transport history of air masses within and outside the polar dome. Air masses within the springtime polar dome mainly experienced diabatic cooling while traveling over cold surfaces. In contrast, air masses in the summertime polar dome were diabatically heated due to insolation. During both seasons air masses outside the polar dome slowly descended into the Arctic lower troposphere from above through radiative cooling. Ascent to the middle and upper troposphere mainly took place outside the Arctic, followed by a northward motion. Air masses inside and outside the polar dome were also distinguished by different chemical compositions of both trace gases and aerosol particles. We found that the fraction of amine-containing particles, originating from Arctic marine biogenic sources, is enhanced inside the polar dome. In contrast, concentrations of refractory black carbon are highest outside the polar dome, indicating remote pollution sources. Synoptic-scale weather systems frequently disturb the transport barrier formed by the polar dome and foster exchange between air masses from midlatitudes and polar regions. During the second phase of the NETCARE 2014 measurements a pronounced low-pressure system south of Resolute Bay brought inflow from southern latitudes, which pushed the polar dome northward and significantly affected trace gas mixing ratios in the measurement region. Mean CO mixing ratios increased from 77.9±2.5 to 84.9±4.7 ppbv between these two regimes. At the same time CO2 mixing ratios significantly decreased from 398.16 ± 1.01 to 393.81 ± 2.25 ppmv. Our results demonstrate the utility of applying a tracer-based diagnostic to determine the polar dome boundary for interpreting observations of atmospheric composition in the context of transport history.

scholarly journals Contrasting molecular diversity and demography patterns in two intertidal amphipod crustaceans reflect Atlantification of High Arctic

2019 ◽  
Vol 166 (12) ◽  
Author(s):  
Michał Grabowski ◽  
Aleksandra Jabłońska ◽  
Agata Weydmann-Zwolicka ◽  
Mikhail Gantsevich ◽  
Petr Strelkov ◽  
...  
Keyword(s):  
Operational Taxonomic Unit ◽  
Molecular Study ◽  
High Arctic ◽  
The Arctic ◽  
Amphipod Species ◽  
Distribution Analysis ◽  
Svalbard Archipelago ◽  
Postglacial Expansion ◽  
Northern Atlantic ◽  
The Last Glacial

Abstract The distribution of two common intertidal amphipod species Gammarus oceanicus and Gammarus setosus was studied along the coast of Svalbard Archipelago. Genetic analysis showed geographical homogeneity of G. oceanicus with only one molecular operational taxonomic unit (MOTU) and much higher diversification of G. setosus (5 MOTUs) in the studied area. Only two MOTUs of G. setosus are widespread along the whole studied Svalbard coastline, whereas the remaining three MOTUs are present mainly along the northern and eastern parts of archipelago’s largest island, Spitsbergen. Distribution analysis indicates that the demographic and spatial expansion of G. oceanicus in the northern Atlantic has started already during the Last Glacial Maximum (LGM, ca. 18 ka), while G. setosus seems to be a long-persistent inhabitant of the Arctic, possibly even through the LGM, with slower distribution dynamics. Combining the results of our molecular study with previous field observations and the knowledge upon the direction of ocean currents around the Svalbard Archipelago, it can be assumed that G. oceanicus is a typical boreal Atlantic species that is still continuing its postglacial expansion northwards. In recent decades it colonized High Arctic due to the climate warming and has partly displaced G. setosus, that used to be the only common gammarid of the Svalbard intertidal zone.

scholarly journals Long-Term Performance Assessment of Low-Cost Atmospheric Sensors in the Arctic Environment

Sensors ◽  
2020 ◽  
Vol 20 (7) ◽  
pp. 1919 ◽  
Author(s):  
Federico Carotenuto ◽  
Lorenzo Brilli ◽  
Beniamino Gioli ◽  
Giovanni Gualtieri ◽  
Carolina Vagnoli ◽  
...  
Keyword(s):  
Particulate Matter ◽  
Relative Humidity ◽  
Air Temperature ◽  
Meteorological Parameters ◽  
Low Cost ◽  
Absolute Error ◽  
Atmospheric Composition ◽  
The Arctic ◽  
Svalbard Archipelago ◽  
Arctic Environment

The Arctic is an important natural laboratory that is extremely sensitive to climatic changes and its monitoring is, therefore, of great importance. Due to the environmental extremes it is often hard to deploy sensors and observations are limited to a few sparse observation points limiting the spatial and temporal coverage of the Arctic measurement. Given these constraints the possibility of deploying a rugged network of low-cost sensors remains an interesting and convenient option. The present work validates for the first time a low-cost sensor array (AIRQino) for monitoring basic meteorological parameters and atmospheric composition in the Arctic (air temperature, relative humidity, particulate matter, and CO2). AIRQino was deployed for one year in the Svalbard archipelago and its outputs compared with reference sensors. Results show good agreement with the reference meteorological parameters (air temperature (T) and relative humidity (RH)) with correlation coefficients above 0.8 and small absolute errors (≈1 °C for temperature and ≈6% for RH). Particulate matter (PM) low-cost sensors show a good linearity (r2 ≈ 0.8) and small absolute errors for both PM2.5 and PM10 (≈1 µg m−3 for PM2.5 and ≈3 µg m−3 for PM10), while overall accuracy is impacted both by the unknown composition of the local aerosol, and by high humidity conditions likely generating hygroscopic effects. CO2 exhibits a satisfying agreement with r2 around 0.70 and an absolute error of ≈23 mg m−3. Overall these results, coupled with an excellent data coverage and scarce need of maintenance make the AIRQino or similar devices integrations an interesting tool for future extended sensor networks also in the Arctic environment.

scholarly journals Simultaneous measurements of aerosol size distributions at three sites in the European high Arctic

2019 ◽  
Vol 19 (11) ◽  
pp. 7377-7395 ◽  
Author(s):  
Manuel Dall'Osto ◽  
David C. S. Beddows ◽  
Peter Tunved ◽  
Roy M. Harrison ◽  
Angelo Lupi ◽  
...  
Keyword(s):  
Cluster Analysis ◽  
Cloud Condensation Nuclei ◽  
High Arctic ◽  
The Arctic ◽  
Research Station ◽  
Size Distributions ◽  
Aerosol Formation ◽  
Condensation Nuclei ◽  
Main Mode ◽  
Accumulation Mode

Abstract. Aerosols are an integral part of the Arctic climate system due to their direct interaction with radiation and indirect interaction through cloud formation. Understanding aerosol size distributions and their dynamics is crucial for the ability to predict these climate relevant effects. When of favourable size and composition, both long-range-transported – and locally formed particles – may serve as cloud condensation nuclei (CCN). Small changes of composition or size may have a large impact on the low CCN concentrations currently characteristic of the Arctic environment. We present a cluster analysis of particle size distributions (PSDs; size range 8–500 nm) simultaneously collected from three high Arctic sites during a 3-year period (2013–2015). Two sites are located in the Svalbard archipelago: Zeppelin research station (ZEP; 474 m above ground) and the nearby Gruvebadet Observatory (GRU; about 2 km distance from Zeppelin, 67 m above ground). The third site (Villum Research Station at Station Nord, VRS; 30 m above ground) is 600 km west-northwest of Zeppelin, at the tip of north-eastern Greenland. The GRU site is included in an inter-site comparison for the first time. K-means cluster analysis provided eight specific aerosol categories, further combined into broad PSD classes with similar characteristics, namely pristine low concentrations (12 %–14 % occurrence), new particle formation (16 %–32 %), Aitken (21 %–35 %) and accumulation (20 %–50 %). Confined for longer time periods by consolidated pack sea ice regions, the Greenland site GRU shows PSDs with lower ultrafine-mode aerosol concentrations during summer but higher accumulation-mode aerosol concentrations during winter, relative to the Svalbard sites. By association with chemical composition and cloud condensation nuclei properties, further conclusions can be derived. Three distinct types of accumulation-mode aerosol are observed during winter months. These are associated with sea spray (largest detectable sizes, >400 nm), Arctic haze (main mode at 150 nm) and aged accumulation-mode (main mode at 220 nm) aerosols. In contrast, locally produced particles, most likely of marine biogenic origin, exhibit size distributions dominated by the nucleation and Aitken mode during summer months. The obtained data and analysis point towards future studies, including apportioning the relative contribution of primary and secondary aerosol formation processes and elucidating anthropogenic aerosol dynamics and transport and removal processes across the Greenland Sea. In order to address important research questions in the Arctic on scales beyond a singular station or measurement events, it is imperative to continue strengthening international scientific cooperation.

scholarly journals Atmospheric black carbon and sulfate concentrations in Northeast Greenland

2015 ◽  
Vol 15 (16) ◽  
pp. 9681-9692 ◽  
Author(s):  
A. Massling ◽  
I. E. Nielsen ◽  
D. Kristensen ◽  
J. H. Christensen ◽  
L. L. Sørensen ◽  
...  
Keyword(s):  
Black Carbon ◽  
Correlation Coefficient ◽  
Seasonal Pattern ◽  
Maximum Level ◽  
High Arctic ◽  
The Arctic ◽  
Research Station ◽  
Summer Period ◽  
Transport Pathways ◽  
Inorganic Matter

Abstract. Measurements of equivalent black carbon (EBC) in aerosols at the high Arctic field site Villum Research Station (VRS) at Station Nord in North Greenland showed a seasonal variation in EBC concentrations with a maximum in winter and spring at ground level. Average measured concentrations were about 0.067 ± 0.071 for the winter and 0.011 ± 0.009 for the summer period. These data were obtained using a multi-angle absorption photometer (MAAP). A similar seasonal pattern was found for sulfate concentrations with a maximum level during winter and spring analyzed by ion chromatography. Here, measured average concentrations were about 0.485 ± 0.397 for the winter and 0.112 ± 0.072 for the summer period. A correlation between EBC and sulfate concentrations was observed over the years 2011 to 2013 stating a correlation coefficient of R2 = 0.72. This finding gives the hint that most likely transport of primary emitted BC particles to the Arctic was accompanied by aging of the aerosols through condensational processes. BC and sulfate are known to have only partly similar sources with respect to their transport pathways when reaching the high Arctic. Aging processes may have led to the formation of secondary inorganic matter and further transport of BC particles as cloud processing and further washout of particles is less likely based on the typically observed transport patterns of air masses arriving at VRS. Additionally, concentrations of EC (elemental carbon) based on a thermo-optical method were determined and compared to EBC measurements. EBC measurements were generally higher, but a correlation between EC and EBC resulted in a correlation coefficient of R2 = 0.64. Model estimates of the climate forcing due to BC in the Arctic are based on contributions of long-range transported BC during spring and summer. The measured concentrations were here compared with model results obtained by the Danish Eulerian Hemispheric Model, DEHM. Good agreement between measured and modeled concentrations of both EBC/BC and sulfate was observed. Also, the correlation between BC and sulfate concentrations was confirmed based on the model results observed over the years 2011 to 2013 stating a correlation coefficient of R2 = 0.74. The dominant source is found to be combustion of fossil fuel with biomass burning as a minor, albeit significant source.

scholarly journals Dynamics of gaseous oxidized mercury at Villum Research Station during the High Arctic summer

2021 ◽  
Vol 21 (17) ◽  
pp. 13287-13309
Author(s):  
Jakob Boyd Pernov ◽  
Bjarne Jensen ◽  
Andreas Massling ◽  
Daniel Charles Thomas ◽  
Henrik Skov
Keyword(s):  
General Pattern ◽  
Ground Level ◽  
High Arctic ◽  
Atmospheric Mercury ◽  
The Arctic ◽  
Research Station ◽  
Cold Temperatures ◽  
Air Masses ◽  
Arctic Summer ◽  
Gaseous Oxidized Mercury

Abstract. While much research has been devoted to the subject of gaseous elemental mercury (GEM) and gaseous oxidized mercury (GOM) in the Arctic spring during atmospheric mercury depletion events, few studies have examined the behavior of GOM in the High Arctic summer. GOM, once deposited and incorporated into the ecosystem, can pose a threat to human and wildlife health, though there remain large uncertainties regarding the transformation, deposition, and assimilation of mercury into the food web. Therefore, to further our understanding of the dynamics of GOM in the High Arctic during the late summer, we performed measurements of GEM and GOM, along with meteorological parameters and atmospheric constituents, and utilized modeled air mass history during two summer campaigns in 2019 and 2020 at Villum Research Station (Villum) in northeastern Greenland. Seven events of enhanced GOM concentrations were identified and investigated in greater detail. In general, the common factors associated with event periods at ground level were higher levels of radiation and lower H2O mixing ratios, accumulated precipitation, and relative humidity (RH), although none were connected with cold temperatures. Non-event periods at ground level each displayed a different pattern in one or more parameters when compared to event periods. Generally, air masses during event periods for both campaigns were colder and drier, arrived from higher altitudes, and spent more time above the mixed layer and less time in a cloud compared to non-events, although some events deviated from this general pattern. Non-event air masses displayed a different pattern in one or more parameters when compared to event periods, although they were generally warmer and wetter and arrived from lower altitudes with little radiation. Coarse-mode aerosols were hypothesized to provide the heterogenous surface for halogen propagation during some of the events, while for others the source is unknown. While these general patterns were observed for event and non-event periods, analysis of individual events showed more specific origins. Five of the seven events were associated with air masses that experienced similar conditions: transported from the cold, dry, and sunlit free troposphere. However, two events experienced contrasting conditions, with air masses being warm and wet with surface layer contact under little radiation. Two episodes of extremely high levels of NCoarse and BC, which appear to originate from flaring emissions in Russia, did not contribute to enhanced GOM levels. This work aims to provide a better understanding of the dynamics of GOM during the High Arctic summer.

scholarly journals 40 years High Arctic climatological dataset of the Polish Polar Station Hornsund (SW Spitsbergen, Svalbard)

2019 ◽  
Author(s):  
Tomasz Wawrzyniak ◽  
Marzena Osuch
Keyword(s):  
Environmental Changes ◽  
High Arctic ◽  
The Arctic ◽  
Data Series ◽  
Annual Data ◽  
Climate Data ◽  
Atlantic Sector ◽  
Svalbard Archipelago

Abstract. The article presents the climatological dataset from the Polish Polar Station Hornsund located in the SW part of Spitsbergen - the biggest island of the Svalbard Archipelago. Due to a general lack of long-term in situ measurements and observations, the high Arctic remains one of the largest climate‐data deficient regions on the Earth, so described series is of unique value. To draw conclusions on the climatic changes in the Arctic, it is necessary to analyse the long-term series of continuous, systematic, in situ observations from different locations and comparing the corresponding data, rather than rely on the climatic simulations only. In recent decades, rapid environmental changes occurring in the Atlantic sector of the Arctic are reflected in the data series collected by the operational monitoring conducted at the Hornsund Station. We demonstrate the results of the 40 years-long series of observations. Climatological mean values or totals are given, and we also examined the variability of meteorological variables at monthly and annual scale using the modified Mann-Kendall test for trend and Sen’s method. The relevant daily, monthly, and annual data are provided on the PANGAEA repository (https://doi.org/10.1594/PANGAEA.909042, Wawrzyniak and Osuch, 2019).

scholarly journals Biogenic and anthropogenic sources of aerosols at the High Arctic site Villum Research Station

2019 ◽  
Vol 19 (15) ◽  
pp. 10239-10256 ◽  
Author(s):  
Ingeborg E. Nielsen ◽  
Henrik Skov ◽  
Andreas Massling ◽  
Axel C. Eriksson ◽  
Manuel Dall'Osto ◽  
...  
Keyword(s):  
Sea Ice ◽  
Organic Aerosol ◽  
High Arctic ◽  
Polar Front ◽  
Anthropogenic Sources ◽  
The Arctic ◽  
Research Station ◽  
Aerosol Formation ◽  
Sea Ice Extent ◽  
Arctic Haze

Abstract. There are limited measurements of the chemical composition, abundance and sources of atmospheric particles in the High Arctic To address this, we report 93 d of soot particle aerosol mass spectrometer (SP-AMS) data collected from 20 February to 23 May 2015 at Villum Research Station (VRS) in northern Greenland (81∘36′ N). During this period, we observed the Arctic haze phenomenon with elevated PM1 concentrations ranging from an average of 2.3, 2.3 and 3.3 µg m−3 in February, March and April, respectively, to 1.2 µg m−3 in May. Particulate sulfate (SO42-) accounted for 66 % of the non-refractory PM1 with the highest concentration until the end of April and decreasing in May. The second most abundant species was organic aerosol (OA) (24 %). Both OA and PM1, estimated from the sum of all collected species, showed a marked decrease throughout May in accordance with the polar front moving north, together with changes in aerosol removal processes. The highest refractory black carbon (rBC) concentrations were found in the first month of the campaign, averaging 0.2 µg m−3. In March and April, rBC averaged 0.1 µg m−3 while decreasing to 0.02 µg m−3 in May. Positive matrix factorization (PMF) of the OA mass spectra yielded three factors: (1) a hydrocarbon-like organic aerosol (HOA) factor, which was dominated by primary aerosols and accounted for 12 % of OA mass, (2) an Arctic haze organic aerosol (AOA) factor and (3) a more oxygenated marine organic aerosol (MOA) factor. AOA dominated until mid-April (64 %–81 % of OA), while being nearly absent from the end of May and correlated significantly with SO42-, suggesting the main part of that factor is secondary OA. The MOA emerged late at the end of March, where it increased with solar radiation and reduced sea ice extent and dominated OA for the rest of the campaign until the end of May (24 %–74 % of OA), while AOA was nearly absent. The highest O∕C ratio (0.95) and S∕C ratio (0.011) was found for MOA. Our data support the current understanding that Arctic aerosols are highly influenced by secondary aerosol formation and receives an important contribution from marine emissions during Arctic spring in remote High Arctic areas. In view of a changing Arctic climate with changing sea-ice extent, biogenic processes and corresponding source strengths, highly time-resolved data are needed in order to elucidate the components dominating aerosol concentrations and enhance the understanding of the processes taking place.

scholarly journals Dynamics of gaseous oxidized mercury at Villum Research Station during the High Arctic summer

2021 ◽  
Author(s):  
Jakob Boyd Pernov ◽  
Bjarne Jensen ◽  
Andreas Massling ◽  
Daniel Charles Thomas ◽  
Henrik Skov
Keyword(s):  
Meteorological Data ◽  
High Arctic ◽  
Atmospheric Mercury ◽  
The Arctic ◽  
Research Station ◽  
Cold Temperatures ◽  
Air Mass ◽  
Back Trajectories ◽  
Arctic Summer ◽  
Gaseous Oxidized Mercury

Abstract. While much research has been devoted to the subject of gaseous elemental mercury (GEM) and gaseous oxidized mercury (GOM) in the Arctic spring, during atmospheric mercury depletion events, few studies have examined the behavior of GOM in the High Arctic summer. GOM, once introduced into the ecosystem, can pose a threat to human and wildlife health, though there remain large uncertainties regarding the transformation, deposition, and assimilation of mercury into the ecosystem. Therefore, to further our understanding of the dynamics of gaseous oxidized mercury in the High Arctic during the late summer, we performed measurements of GEM and GOM along with meteorological parameters, atmospheric constituents, and air mass history during two summer campaigns in 2019 and 2020 at Villum Research Station (Villum) in Northeastern Greenland. Five events of enhanced GOM concentrations were identified and investigated in greater detail. The origin of these events was identified, through analysis of air mass back-trajectories, associated meteorological data, and other atmospheric constituents, to be the cold, dry free troposphere. These events were associated with low RH, limited precipitation, cold temperatures, and intense sunlight along the trajectory path. Events were positively correlated with ozone, aerosol particle number, and black carbon mass concentration, which were interpreted as an indication of tropospheric air masses. This work aims to provide a better understanding of the dynamics of GOM during the High Arctic summer.

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