Description: This paper presents the results of measurements of aerosol physical and chemical properties during iAREA2014 campaign that took place on Svalbard between 15th of Mar and 4th of May 2014. With respect to field area, the experiment consisted of two sites: NyeÅlesund (78�550N, 11�560E) and Longyearbyen (78�130N, 15�330E) with further integration of Aerosol Robotic Network (AERONET) station in Hornsund (77�000N, 15�330E). The subject of this study is to investigate the inesitu, passive and active remote sensing observations as well as numerical simulations to describe the temporal variability of aerosol singleescattering properties during spring season on Spitsbergen. The retrieval of the data indicates several event days with enhanced singleescattering properties due to the existence of sulphate and additional seaesalt load in the atmosphere which is possibly caused by relatively high wind speed. Optical results were confirmed by numerical simulations made by the GEMeAQ model and by chemical observations that indicated up to 45% contribution of the seaesalt to a PM10 total aerosol mass concentration. An agreement between the in-situ optical and microphysical properties was found, namely: the positive correlation between aerosol scattering coefficient measured by the nephelometer and effective radius obtained from laser aerosol spectrometer as well as negative correlation between aerosol scattering coefficient and the Ångstrom exponent indicated that slightly larger particles dominated during special events. The inesitu surface observations do not show any significant enhancement of the absorption coefficient as well as the black carbon concentration which might occur during spring. All of extensive singleescattering properties indicate a diurnal cycle in Longyearbyen, where 21:00e5:00 data stays at the background level, however increasing during the day by the factor of 3e4. It is considered to be highly connected with local emissions originating in combustion, traffic and harbour activities. On the other hand, no daily fluctuations in NyeÅlesund are observed. Mean values in NyeÅlesund are equal to 8.2, 0.8 Mm�1 and 103 ng/m3 for scattering, absorption coefficients and black carbon concentration; however in Longyearbyen (only data from 21:00e05:00 UTC) they reach 7.9, 0.6 Mm�1 as well as 83 ng/ m3 respectively. Overall, the spring 2014 was considerably clean and seaesalt was the major aerosol component

Description: In this work, a closure experiment for tropospheric aerosol is presented. Aerosol size distributions and single scattering albedo from remote sensing data are compared to those measured in-situ. An aerosol pollution event on 4 April 2009 was observed by ground based and airborne lidar and photometer in and around Ny-Ålesund, Spitsbergen, as well as by DMPS, nephelometer and particle soot absorption photometer at the nearby Zeppelin Mountain Research Station. The presented measurements were conducted in an area of 40 20 km around Ny-Ålesund as part of the 2009 Polar Airborne Measurements and Arctic Regional Climate Model Simulation Project (PAMARCMiP). Aerosol mainly in the accumulation mode was found in the lower troposphere, however, enhanced backscattering was observed up to the tropopause altitude. A comparison of meteorological data available at different locations reveals a stable multi-layer-structure of the lower troposphere. It is followed by the retrieval of optical and microphysical aerosol parameters. Extinction values have been derived using two different methods, and it was found that extinction (especially in the UV) derived from Raman lidar data significantly surpasses the extinction derived from photometer AOD profiles. Airborne lidar data shows volume depolarization values to be less than 2.5% between 500 m and 2.5 km altitude, hence, particles in this range can be assumed to be of spherical shape. In-situ particle number concentrations measured at the Zeppelin Mountain Research Station at 474m altitude peak at about 0.18 mmdiameter, which was also found for the microphysical inversion calculations performed at 850 m and 1500 m altitude. Number concentrations depend on the assumed extinction values, and slightly decrease with altitude as well as the effective particle diameter. A low imaginary part in the derived refractive index suggests weakly absorbing aerosols, which is confirmed by low black carbon concentrations, measured at the Zeppelin Mountain as well as on board the Polar 5 aircraft.

Description: The Arctic atmospheric boundary layer (AABL) in the central Arctic was characterized by dropsonde, lidar, ice thickness and airborne in situ measurements during the international Polar Airborne Measurements and Arctic Regional Climate Model Simulation Project (PAMARCMiP) in April 2009. We discuss AABL observations in the lowermost 500 m above (A) open water, (B) sea ice with many open/refrozen leads (C) sea ice with few leads, and (D) closed sea ice with a front modifying the AABL. Above water, the AABL had near-neutral stratification and contained a high water vapor concentration. Above sea ice, a low AABL top, low near-surface temperatures, strong surface-based temperature inversions and an increase of moisture with altitude were observed. AABL properties and particle concentrations were modified by a frontal system, allowing vertical mixing with the free atmosphere. Above areas with many leads, the potential temperature decreased with height in the lowest 50 m and was nearly constant above, up to an altitude of 100–200 m, indicating vertical mixing. The increase of the backscatter coefficient towards the surface was high. Above sea ice with few refrozen leads, the stably stratified boundary layer extended up to 200–300 m altitude. It was characterized by low specific humidity and a smaller increase of the backscatter coefficient towards the surface.

Description: Aircraft borne optical in situ size distribution measurements were performed within Arctic boundary layer clouds with a special emphasis on the cloud top layer during the VERtical Distribution of Ice in Arctic clouds (VERDI) campaign in April and May 2012. An instrumented Basler BT-67 research aircraft operated out of Inuvik over the Mackenzie River delta and the Beaufort Sea in the Northwest Territories of Canada. Besides the cloud particle and hydrometeor size spectrometers the aircraft was equipped with instrumentation for aerosol, radiation and other parameters. Inside the cloud, droplet size distributions with monomodal shapes were observed for predominantly liquid-phase Arctic stratocumulus. With increasing altitude inside the cloud the droplet mean diameters grew from 10 to 20 μm. In the upper transition zone (i.e., adjacent to the cloud-free air aloft) changes from monomodal to bimodal droplet size distributions (Mode 1 with 20 μm and Mode 2 with 10 μm diameter) were observed. It is shown that droplets of both modes co-exist in the same (small) air volume and the bimodal shape of the measured size distributions cannot be explained as an observational artifact caused by accumulating data point populations from different air volumes. The formation of the second size mode can be explained by (a) entrainment and activation/condensation of fresh aerosol particles, or (b) by differential evaporation processes occurring with cloud droplets engulfed in different eddies. Activation of entrained particles seemed a viable possibility as a layer of dry Arctic enhanced background aerosol (which was detected directly above the stratus cloud) might form a second mode of small cloud droplets. However, theoretical considerations and model calculations (adopting direct numerical simulation, DNS) revealed that, instead, turbulent mixing and evaporation of larger droplets are the most likely reasons for the formation of the second droplet size mode in the uppermost region of the clouds.

Description: On December 6, 2002, during winter darkness, an extraordinary event occured in the sky as viewed from Longyearbyen (78°N, 15°E), Svalbard, Norway. At 07:30 UT the South - East sky was surprisingly lit up in a deep red colour. The light increased in intensity and spread out across the sky, and at 10:00 UT the illumination was observed to reach the zenith. The event died out at about 12:30 UT. Spectral measurements from the Auroral Station in Adventdalen confirm that the light was scattered sunlight. Even though the Sun was between 11.8 and 14.6 degrees below the horizon during the event, the measured intensities of scattered light on the southern horizon from the scanning photometers coincided with the rise and setting of the Sun. Calculations of actual heights, including refraction and atmospheric screening, indicate that the event most likely is scattered solar light from a target below the horizon. This is also confirmed by the OSIRIS instrument onboard the Odin satellite. The deduced height profile indicates that the scattering target is located 20-25 km up in the Stratosphere at a latitude close to 73 - 75°N, South - East of Longyearbyen. The temperatures in this region were found to be low enough for Polar Stratospheric Clouds (PSC) to be formed. The target was also identified as PSC by the LIDAR systems at the Koldewey Station in Ny-Ålesund (79°N, 12°E). The event is most likely caused by solar illuminated type II Polar Stratospheric Clouds that scattered light towards Svalbard. Two types of scenarios are presented to explain how light is scattered.

Description: Biomass burning related aerosol episodes are becoming a serious threat to the radiative balance of the Arctic region. Since early July 2017 intense wildfires were recorded between August and September in Canada and Greenland, covering an area up to 4674 km2 in size. This paper describes the impact of these biomass burning (BB) events measured over Svalbard, using an ensemble of ground-based, columnar, and vertically-resolved techniques. BB influenced the aerosol chemistry via nitrates and oxalates, which exhibited an increase in their concentrations in all of size fractions, indicating the BB origin of particles. The absorption coefficient data (530 nm) at ground reached values up to 0.6 Mm–1, highlighting the impact of these BB events when compared to average Arctic background values, which do not exceed 0.05 Mm–1. The absorption behavior is fundamental as implies a subsequent atmospheric heating. At the same time, the AERONET Aerosol Optical Depth (AOD) data showed high values at stations located close to or in Canada (AOD over 2.0). Similarly, increased values of AODs were then observed in Svalbard, e.g., in Hornsund (daily average AODs exceeded 0.14 and reached hourly values up to 0.5). Elevated values of AODs were then registered in Sodankylä and Andenes (daily average AODs exceeding 0.150) a few days after the Svalbard observation of the event highlighting the BB columnar magnitude, which is crucial for the radiative impact. All the reported data suggest to rank the summer 2017 plume of aerosols as one of the biggest atmosphere related environmental problems over Svalbard region in last 10 years

Description: The synergy between airborne lidar, radar, passive microwave, and passive imaging spectrometer measurements was used to characterize the vertical and small-scale (down to 10 m) horizontal distribution of the cloud thermodynamic phase. Two case studies of low-level Arctic clouds in a cold air outbreak and a warm air advection observed during the Arctic CLoud Observations Using airborne measurements during polar Day (ACLOUD) were investigated. Both clouds exhibited the typical vertical mixed-phase structure with mostly liquid water droplets at cloud top and ice crystals in lower layers. The cloud top horizontal small-scale variability observed during the cold air outbreak is dominated by the liquid water close to the cloud top and shows no indication of ice in lower cloud layers. Contrastingly, the cloud top variability of the case observed during a warm air advection showed some ice in areas of low reflectivity or cloud holes. Radiative transfer simulations considering homogeneous mixtures of liquid water droplets and ice crystals were able to reproduce the horizontal variability of this warm air advection. To account for more realistic vertical distributions of the thermodynamic phase, large eddy simulations (LES) were performed to reconstruct the observed cloud properties and were used as input for radiative transfer simulations. The simulations of the cloud observed during the cold air outbreak, with mostly liquid water at cloud top, realistically reproduced the observations. For the warm air advection case, the simulated cloud field underestimated the ice water content (IWC). Nevertheless, it revealed the presence of ice particles close to the cloud top and confirmed the observed horizontal variability of the cloud field. It is concluded that the cloud top small-scale horizontal variability reacts to changes in the vertical distribution of the cloud thermodynamic phase. Passive satellite-borne imaging spectrometer observations with pixel sizes larger than 100 m miss the small-scale cloud top structures, which limits their capabilities to provide indications about the cloud vertical structure.