Interannual and seasonal variations in the aerosol optical depth of the atmosphere in two regions of Spitsbergen (2002–2018)

In this work, hourly averaged sun photometer data from Barentsburg and Ny-Ålesund, both located on Spitsbergen in the European Arctic, are compared. Our data set comprises the years from 2002 to 2018 with overlapping measurements from both sites during the period from 2011 to 2018. For more turbid periods (aerosol optical depth, AOD, τ0.5>0.1), we found that Barentsburg is typically more polluted than Ny-Ålesund, especially in the shortwave spectrum. However, the diurnal variation in the AOD is highly correlated. Next, τ was divided into a fine and coarse mode. It was found that the fine-mode aerosol optical depth generally dominates and also shows a larger interannual than seasonal variation. The fine-mode optical depth is in fact largest in spring during the Arctic haze period. Overall the aerosol optical depth seems to decrease (at 500 nm the fine-mode optical depth decreased by 0.016 over 10 years), although this is hardly statistically significant

Comparison of atmospheric aerosol optical depths measured with different sun photometers in three regions of Spitsbergen Archipelago

Results of multiyear (2011-2017) aerosol monitoring were used to compare the spectral aerosol optical depths (AOD) of the atmosphere, measured with different sun photometers at three Arctic stations on Spitsbergen Archipelago: Hornsund, Barentsburg, Ny-Ålesund. In addition to agreement of data in three regions, we also found that AOD in Barentsburg slightly (comparable to error) exceeds those from other stations located 110-120 km away. The AOD discrepancy is more pronounced in the shortwave part of the spectrum, indicating more abundant fine-mode aerosol in Barentsburg

Spatiotemporal Variations of Aerosol Optical Depth in the Atmosphere over Baikal Region Based on MODIS Data

This paper considers spatiotemporal distribution and seasonal variability of aerosol optical depth (AOD) of the atmosphere at the 0.55 μm wavelength in the atmosphere over the Baikal region of Russia based on long-term data (2005–2019) from satellite observations (MODIS/AQUA). A comparison of satellite AOD values with the AERONET record at the Geophysical Observatory of Institute of Solar-Terrestrial Physics of Siberian Brunch of Russian Academy of Science was performed. The results show that interannual AOD variability is mainly due to forest fires. The highest atmospheric transparency was in 2010, 2013 and 2016, and the lowest was in 2008, 2012 and 2014. It is noted that AOD decreased with latitude with a gradient ΔAOD = 0.002 ÷ 0.001 per degree of latitude. The mean seasonal variations in AOD at the six satellite overpass points were characterized by spring (April) and summer (July) highs and low AOD values in autumn. From June to November, the drop in AOD monthly means was more than 60%

Spatiotemporal Variations of Aerosol Optical Depth in the Atmosphere over Baikal Region Based on MODIS Data

This paper considers spatiotemporal distribution and seasonal variability of aerosol optical depth (AOD) of the atmosphere at the 0.55 μm wavelength in the atmosphere over the Baikal region of Russia based on long-term data (2005–2019) from satellite observations (MODIS/AQUA). A comparison of satellite AOD values with the AERONET record at the Geophysical Observatory of Institute of Solar-Terrestrial Physics of Siberian Brunch of Russian Academy of Science was performed. The results show that interannual AOD variability is mainly due to forest fires. The highest atmospheric transparency was in 2010, 2013 and 2016, and the lowest was in 2008, 2012 and 2014. It is noted that AOD decreased with latitude with a gradient ΔAOD = 0.002 ÷ 0.001 per degree of latitude. The mean seasonal variations in AOD at the six satellite overpass points were characterized by spring (April) and summer (July) highs and low AOD values in autumn. From June to November, the drop in AOD monthly means was more than 60%

Spatial Distribution of Atmospheric Aerosol Physicochemical Characteristics in the Russian Sector of the Arctic Ocean

The results from studies of aerosol in the Arctic atmosphere are presented: the aerosol optical depth (AOD), the concentrations of aerosol and black carbon, as well as the chemical composition of the aerosol. The average aerosol characteristics, measured during nine expeditions (2007–2018) in the Eurasian sector of the Arctic Ocean, had been 0.068 for AOD (0.5 µm); 2.95 cm−3 for particle number concentrations; 32.1 ng/m3 for black carbon mass concentrations. Approximately two–fold decrease of the average characteristics in the eastern direction (from the Barents Sea to Chukchi Sea) is revealed in aerosol spatial distribution. The average aerosol characteristics over the Barents Sea decrease in the northern direction: black carbon concentrations by a factor of 1.5; particle concentrations by a factor of 3.7. These features of the spatial distribution are caused mainly by changes in the content of fine aerosol, namely: by outflows of smokes from forest fires and anthropogenic aerosol. We considered separately the measurements of aerosol characteristics during two expeditions in 2019: in the north of the Barents Sea (April) and along the Northern Sea Route (July–September). In the second expedition the average aerosol characteristics turned out to be larger than multiyear values: AOD reached 0.36, particle concentration up to 8.6 cm−3, and black carbon concentration up to 179 ng/m3. The increased aerosol content was affected by frequent outflows of smoke from forest fires. The main (99%) contribution to the elemental composition of aerosol in the study regions was due to Ca, K, Fe, Zn, Br, Ni, Cu, Mn, and Sr. The spatial distribution of the chemical composition of aerosols was analogous to that of microphysical characteristics. The lowest concentrations of organic and elemental carbon (OC, EC) and of most elements are observed in April in the north of the Barents Sea, and the maximal concentrations in Far East seas and in the south of the Barents Sea. The average contents of carbon in aerosol over seas of the Asian sector of the Arctic Ocean are OC = 629 ng/m3, EC = 47 ng/m3

Radiative Characteristics of Aerosol During Extreme Fire Event over Siberia in Summer 2012

Microphysical and optical properties of aerosol were studied during a mega-fire event in summer 2012 over Siberia using ground-based measurements of spectral solarradiation at the AERONET site in Tomsk and satellite observations. The data were analyzed using multi-year (2003-2013) measurements of aerosol characteristics under back-ground conditions and for less intense fires, differing in burning biomass type, stage of fire, remoteness from observation site, etc. (ordinary smoke). In June-August 2012, the average aerosol optical depth (AOD, 500 nm) had been 0.95+/-0.86, about a factor of 6 larger than background values (0.16+/-0.08), and a factor of 2.5 larger than in ordinary smoke. The AOD values were extremely high on 24-28 July and reached 3-5. A comparison with satellite observations showed that ground-based measurements in the region of Tomsk not only reflect the local AOD features, but are also characteristic for the territory of Western Siberia as a whole. Single scattering albedo (SSA, 440 nm) in this period ranged from 0.91 to 0.99 with an average of approx. 0.96 in the entire wavelength range of 440-1020 nm. The increase in absorptance of aerosol particles (SSA(440 nm)=0.92) and decrease in SSA with wavelength observed in ordinary smoke agree with the data from multi-year observations in analogous situations in the boreal zone of USA and Canada. Volume aerosol size distribution in extreme and ordinary smoke had a bimodal character with significant prevalence of fine-mode particles, but in summer 2012 the mean median radius and the width of the fine-mode distribution somewhat increased. In contrast to data from multi-year observations, in summer 2012 an increase in the volume concentration and median radius of the coarse mode was observed with growing AOD

Spatio-Temporal Distributions of the Natural Non-Sea-Salt Aerosol Over the Southern Ocean and Coastal Antarctica and Its Potential Source Regions

International audienceMore than 40 years of aerosol data including concentrations of particle number and of nine major ions collected over the Southern Ocean and coastal stations have been aggregated and filtered with back trajectories to reduce the risk of influence from adjacent continents. That provided a rich dataset including latitudinal distribution and seasonality of physical and chemical aerosol parameters that allow insights into aerosol sources over the Southern Ocean. These data together with statistics of back trajectory paths of high (75% percentile) and low (25% percentile) concentrations of the studied aerosol parameters were used to identify potential source regions of the respective compounds. For particle number concentrations, MSA, and the non-seasalt fractions of Ca and potassium the most prominent source regions were found in high DMS-areas close to Antarctica, whereas the potential source regions of NH 4 and the non-sea-salt fraction of Mg were located in part further north over the Southern Ocean. These geographical differences would reflect differences in the marine biota

Spatial Distribution of Aerosol Characteristics over the South Atlantic and Southern Ocean Using Multiyear (2004–2021) Measurements from Russian Antarctic Expeditions

Since 2004, we have carried out yearly measurements of physicochemical aerosol characteristics onboard research vessels at Southern Hemisphere high latitudes (34–72° S; 45° W–110° E). In this work, we statistically generalize the results from multiyear (2004–2021) measurements in this area of the aerosol optical depth (AOD) of the atmosphere, concentrations of aerosol and equivalent black carbon (EBC), as well as the ionic composition of aerosol. A common regularity was that the aerosol characteristics decreased with increasing latitude up to the Antarctic coast, where the aerosol content corresponded to the global background level. Between Africa and Antarctica, AOD decreased from 0.07 to 0.024, the particle volume decreased from 5.5 to 0.55 µm3/cm3, EBC decreased from 68.1 to 17.4 ng/m3, and the summed ion concentration decreased from 24.5 to 2.5 µg/m3. Against the background of the common tendency of the latitude decrease in aerosol characteristics, we discerned a secondary maximum (AOD and ion concentrations) or a plateau (aerosol and EBC concentrations). The obtained spatial distribution of aerosol characteristics qualitatively agreed with the model-based MERRA-2 reanalysis data, but showed quantitative differences: the model AOD values were overestimated (by 0.015, on average); while the EBC concentrations were underestimated (by 21.7 ng/m3). An interesting feature was found in the aerosol spatial distribution in the region of Antarctic islands: at a distance of 300 km from the islands, the concentrations of EBC decreased on average by 29%, while the aerosol content increased by a factor of 2.5

Spatial Distribution of Black Carbon Concentrations in the Atmosphere of the North Atlantic and the European Sector of the Arctic Ocean

We discuss the measurements of black carbon concentrations in the composition of atmospheric aerosol over the seas of the North Atlantic and European sector of the Arctic Ocean (21 expeditions in 2007–2020). The black carbon concentrations were measured by an aethalometer and filter method. The comparison of the two variants of the measurements of the black carbon concentrations showed that the data acceptably agreed and can be used jointly. It is noted that the spatial distribution of black carbon over the ocean is formed under the influence of outflows of air masses from the direction of continents, where the main sources of emission of absorbing aerosol are concentrated. We analyzed the statistical characteristics of black carbon concentrations in five marine regions, differing by the outflows of continental aerosol. The largest black carbon content is a salient feature of the atmosphere of the North and Baltic Seas, surrounded by land: average values of concentrations are 210 ng/m3, and modal values are 75 ng/m3. In other regions (except in the south of the Barents Sea), the average black carbon concentrations are 37–44 ng/m3 (modal concentrations are 18–26 ng/m3). We discuss the specific features of the spatial (latitude-longitude) distributions of black carbon concentrations, relying on ship-based measurements and model calculations (MERRA-2 reanalysis data). A common regularity of the experimental and model spatial distributions of black carbon is that the concentrations decrease in the northern direction and with the growing distance from the continent: from several hundred ng/m3 in the southern part of the North Sea to values below 50 ng/m3 in polar regions of the ocean