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The optical, physical, and chemical properties of aerosol particles have been previously studied in the United Arab Emirates (UAE), but there is still a gap in the knowledge of particle sources and in the horizontal and vertical transport of aerosol particles and their precursors in the area. To investigate how aerosol particle and SO2 concentrations at the surface responded to changes in horizontal and vertical transport, we used data from a 1-year measurement campaign at a background site where local sources of SO2 were expected to be minimal. The measurement campaign provided a combination of in situ measurements at the surface and the boundary layer evolution from vertical and horizontal wind profiles measured by a Doppler lidar. The diurnal structure of the boundary layer in the UAE was very similar from day to day, with a deep, well-mixed boundary layer during the day transitioning to a shallow nocturnal layer, with the maximum boundary layer height usually being reached around 14:00 local time. Both SO2 and nucleation-mode aerosol particle concentrations were elevated for surface winds coming from the east or western sectors. We attribute this to oil refineries located on the eastern and western coasts of the UAE. The concentrations of larger cloud condensation nuclei (CCN)-sized particles and their activation fraction did not show any clear dependence on wind direction, but the CCN number concentration showed some dependence on wind speed, with higher concentrations coinciding with the weakest surface winds. Peaks in SO2 concentrations were also observed despite low surface wind speeds and wind directions unfavourable for transport. However, winds aloft were much stronger, with wind speeds of 10ms-1 at 1 km common at night and wind directions favourable for transport; surface-measured concentrations increased rapidly once these particular layers started to be entrained into the growing boundary layer, even if the surface wind direction was from a clean sector. These conditions also displayed higher nucleation-mode aerosol particle concentrations, i.e. new particle formation events occurring due to the increase in the gaseous precursor. [ABSTRACT FROM AUTHOR]

Abstract. Aerosol particle optical, physical and chemical properties have been previously studied in the United Arab Emirates (UAE), but there is still a gap in the knowledge of particle sources, and in the horizontal and vertical transport of aerosol particles and their precursors in the area. To investigate how aerosol particle and SO2 concentrations at the surface responded to changes in horizontal and vertical transport, we used data from a one-year measurement campaign at a background site where local sources of SO2 where expected to be minimal. The measurement campaign provided a combination of in-situ measurements at the surface, and the boundary layer evolution from vertical and horizontal wind profiles measured by a Doppler lidar. The diurnal structure of the boundary layer in the UAE was very similar from day to day, with deep well-mixed boundary layer during the day transitioning to a shallow nocturnal layer, with the maximum boundary layer height usually being reached around 1400 local time. Both SO2 and nucleation mode aerosol particle concentrations were elevated for surface winds coming from the east or western sectors.We attribute this to oil refineries located on the eastern and western coasts of the UAE. The concentrations of larger cloud condensation nuclei (CCN) sized particles and their activation fraction did not show any clear dependence on wind direction, but the CCN number concentration showed some dependence on wind speed, with higher concentrations coinciding with the weakest surface winds. Peaks in SO2 concentrations were also observed despite low surface wind speeds and wind directions unfavourable for transport. However, winds aloft were much stronger, with wind speeds of 10 m s−1 at 1 km common at night, and with wind directions favourable for transport, and surface-measured concentrations increased rapidly once these particular layers started to be entrained into the growing boundary layer, even if the surface wind direction was from a clean sector. These conditions also displayed higher nucleation mode aerosol particle concentrations, i.e. new particle formation events occurring due to the increase in the gaseous precursor. [ABSTRACT FROM AUTHOR]

Optical properties of surface aerosols at Dome C, Antarctica in 2007-2013 and their potential source areas are presented. Scattering coefficients (ssp) were calculated from measured particle number size distributions with a Mie code and from filter samples using mass scattering efficiencies. Absorption coefficients (sap) were determined with a 3-wavelength Particle Soot Absorption Photometer (PSAP) and corrected for scattering by using two different algorithms. The scattering coefficients were also compared with ssp measured with a nephelometer at the South Pole Station (SPO). The minimum sap was observed in the austral autumn and the maximum in the austral spring, similar to other Antarctic sites. The darkest aerosol, i.e., the lowest single scattering albedo ?o ˜ 0.91 was observed in September and October and the highest ?o ˜ 0.99 in February and March. The uncertainty of the absorption Ångström exponent aap is high. The lowest aap monthly medians were observed in March and the highest in August – October. The equivalent black carbon (eBC) mass concentrations were compared with eBC measured at three other Antarctic sites: the SPO and two coastal sites, Neumayer and Syowa. The maximum monthly median eBC concentrations are almost the same (~3 ± 1 ng m-3 ) at all these sites in October-November. This suggests that there is no significant difference in eBC between the coastal and plateau sites. The seasonal cycle of the eBC mass fraction exhibits a minimum f(eBC) ˜ 0.1% in February-March and a maximum ~4-5% in August-October. Source areas were calculated using 50-day FLEXPART footprints. The highest eBC concentrations and the lowest ?o were associated with air masses coming from South America, Australia and Africa. Vertical simulations that take BC particle removal processes into account show that there would be essentially no BC particles arriving at Dome C from north of latitude 10°S at altitudes < 1600 m. The main biomass-burning regions Africa, Australia and Brazil are more to the south and their smoke plumes have been observed at higher altitudes than that so they can get transported to Antarctica. The seasonal cycle of BC emissions from wildfires and agricultural burning and other fires in South America, Africa and Australia were calculated from data downloaded from the Global Fire Emissions Database (GFED). The maximum total emissions were in August-September but the peak of monthly average eBC concentrations is observed 2 – 3 months later in November not only at Dome C but also at SPO and the coastal stations. The air mass residence-time-weighted BC emissions from South America are approximately an order of magnitude larger than from Africa and Oceania suggesting that South American BC emissions are the largest contributors to eBC at Dome C. At Dome C the maximum and minimum scattering coefficients were observed in austral summer and winter, respectively. At SPO ssp was similar to that observed at Dome C in the austral summer but there was a large difference in winter, suggesting that in winter SPO is more influenced by sea spray emissions than Dome C. The seasonal cycles of ssp at Dome C and at the SPO were compared with the seasonal cycles of secondary and primary marine aerosol emissions. The ssp measured at SPO correlated much better with the sea-spray aerosol emission fluxes in the Southern Ocean than ssp at Dome C. The seasonal cycles of biogenic secondary aerosols were estimated from monthly average phytoplankton biomass concentrations obtained from the CALIOP satellite sensor data. The analysis suggests that a large fraction of the biogenic scattering aerosol observed at Dome C has been formed in the polar zone but it may take a month for the aerosol to be formed, grown and get transported from the sea level to Dome C. [ABSTRACT FROM AUTHOR]

Aerosol particles play an important in role in the microphysics of clouds and hence on their likelihood to precipitate. In the changing climate already dry areas such as the United Arab Emirates (UAE) are predicted to become even drier. Comprehensive observations of the daily and seasonal variation in aerosol particle properties in such locations are required reducing the uncertainty in such predictions. We analyse observations from a one-year measurement campaign at a background location in the United Arab Emirates to investigate the properties of aerosol particles in this region, study the impact of boundary layer mixing on background aerosol particle properties measured at the surface and study the temporal evolution of the aerosol particle cloud formation potential in the region. We used in-situ aerosol particle measurements to characterise the aerosol particle composition, size, number and cloud condensation nuclei (CCN) properties, in-situ SO2 measurements as an anthropogenic signature and a long-range scanning Doppler lidar to provide vertical profiles of the horizontal wind and turbulent properties to monitor the evolution of the boundary layer. Anthropogenic sulphate dominated the aerosol particle mass composition in this location. There was a clear diurnal cycle in the surface wind direction, which had a strong impact on aerosol particle total number concentration, SO2 concentration and black carbon mass concentration. Local sources were the predominant source of black carbon, as concentrations clearly depended on the presence of turbulent mixing, with much higher values during calm nights. The measured concentrations of SO2, instead, were highly dependent on the surface wind direction as well as on the depth of the boundary layer when entrainment from the advected elevated layers occurred. The wind direction at the surface or of the elevated layer suggests that the cities of Dubai, Abu Dhabi and other coastal conurbations were the remote sources of SO2. We observed new aerosol particle formation events almost every day (on four days out of five on average). Calm nights had the highest CCN number concentrations and lowest κ values and activation fractions. We did not observe any clear dependence of CCN number concentration and κ parameter on the height of the daytime boundary layer, whereas the activation fraction did show a slight increase with increasing boundary layer height, due to the change in the shape of the aerosol particle size distribution where the relative portion of larger aerosol particles increased with increasing boundary layer height. We believe that this indicates that size is more important than chemistry for aerosol particle CCN activation at this site. The combination of instrumentation used in this campaign enabled us to identify periods when anthropogenic pollution from remote sources that had been transported in elevated layers was present, and had been mixed down to the surface in the growing boundary layer. [ABSTRACT FROM AUTHOR]

Long-term measurements of black carbon (BC) are warranted for investigating changes in its emission, transport, and deposition. However, depending on instrumentation, parameters related to BC such as aerosol absorption coefficient (babs) have been measured instead. Most ground-based measurements of babs in the Arctic have been made by filter-based absorption photometers, including multi-angle absorption photometers (MAAP), particle soot absorption photometers (PSAP), continuous light absorption photometer (CLAP), and Aethalometers. The measured babs can be converted to atmospheric mass concentrations of BC (MBC) by assuming the value of the mass absorption cross section (MAC = babs/MBC). However, the accuracy of conversion of babs to MBC has not been adequately assessed. Here, we introduce a systematic method for deriving MAC values from babs measured by these instruments and independently measured MBC. In this method, MBC was measured with a filter-based absorption photometer with a heated inlet (COSMOS). COSMOS- derived MBC (MBC (COSMOS)) is traceable to a rigorously calibrated single particle soot photometer (SP2) and the absolute accuracy of MBC (COSMOS) has been demonstrated previously to be about 15 % in Asia and the Arctic. The necessary conditions for application of this method are a high correlation of the measured babs with independently measured MBC, and long-term stability of the correlation slope, which represents the MAC. In general, babs - MBC (COSMOS) correlations were high (r² = 0.84-0.96 for hourly data) at Fukue in Japan, Barrow in Alaska, Ny-Ålesund in Svalbard, Pallastunturi in Finland, and Alert in Canada, and stable up to for 10 years. We successfully estimated MAC values (11.0-15.2 m² g-1 at a wavelength of 550 nm) for these instruments and these MAC values can be used to obtain error-constrained estimates of MBC from babs measured at these sites even in the past, when COSMOS measurements were not made. Because the absolute values of MBC in these Arctic sites estimated by this method are consistent with each other, they are applicable to study spatial and temporal variation of MBC and to evaluate performance of numerical model calculations. [ABSTRACT FROM AUTHOR]

The Arctic absorbing aerosols have a high potential to accelerate global warming. Accurate and sensitive measurements of their concentrations, variability and atmospheric mixing are needed. Filter-based aerosol light absorption measurement methods are the most widely applied in the Arctic. Those will be the focus of this study. Aerosol light absorption was measured during one month field campaign in June–July 2019 at the Pallas Global AtmosphericWatch (GAW) station in northern Finland. The campaign provided a real-world test for different absorption measurement techniques supporting the goals of the EMPIR BC metrology project in developing aerosol absorption standard and reference methods. Very low aerosol concentrations prevailed during the campaign which imposed a challenge for the instruments detection. In this study we compare the results from five filter-based absorption techniques: Aethalometer models AE31 and AE33, Particle Soot Absorption Photometer (PSAP), Multi Angle Absorption Photometer (MAAP) and Continuous Soot Monitoring System (COSMOS), and from one indirect method called Extinction Minus Scattering (EMS). The sensitivity of the filter-based techniques was adequate to measure aerosol light absorption coefficients down to around 0.05 Mm-1 levels. The average value measured during the campaign using MAAP was 0.09 Mm-1 (at wavelength of 637 nm). When data were averaged for >1h, an agreement of around 20% was obtained between instruments. COSMOS measured systematically the lowest absorption coefficient values, which was expected due to the sample pre-treatment in COSMOS inlet. PSAP showed the best linear correlation with MAAP (R2 = 0.85), followed by AE33 and COSMOS (R2 = 0.84). The noisy data from AE31 resulted in a slightly lower, yet a significant, correlation with MAAP (R2 = 0.46). In contrast to the filter-based techniques, the sensitivity of the indirect EMS method to measure aerosol absorption was not adequate at such low concentrations levels. An absorption coefficient on the order of >1 Mm-1 was estimated as the lowest limit, to reliably distinguish the signal from the noise. Throughout the campaign the aerosol was highly scattering with an average single-scattering albedo of 0.97. Two different air-mass origins could be identified: the north-east and from the north-west. The north-eastern air masses contained higher fraction of thickly coated light absorbing particles than the westerly air masses. Aerosol scattering, absorption and the particle coating thickness increased on the last ten days of the campaign during the north-eastern air flow. The simultaneous changes in aerosol source region, mixing state, concentration and particle optical size were reflected in the instruments' response in a complex way. The observed decrease in aerosol size suggested additional activation of secondary particle formation mechanisms. The results demonstrate the challenges encountered in the Arctic absorbing aerosol measurements. The applicability and uncertainties of different techniques are discussed and new knowledge on the absorbing aerosol characteristics in summer Arctic air masses reference to the source region is provided. [ABSTRACT FROM AUTHOR]

Following the emergence of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for COVID-19 in December 2019 in Wuhan (China) and its spread to the rest of the world, the World Health Organization declared a global pandemic in March 2020. Without effective treatment in the initial pandemic phase, social distancing and mandatory quarantines were introduced as the only available preventative measure. Despite the socioeconomic impacts, air quality improved due to lower pollutant emissions. Here we investigate the effects of the COVID-19 lockdowns on ambient black carbon (BC), which affects climate and damages health, using in-situ observations from 17 European stations in a Bayesian inversion framework. BC emissions declined by 11 % in Europe (20 % in Italy, 32 % in Germany, 20 % in Spain) during lockdown compared to the same period in the previous five years. BC temporal variation in the countries enduring the most drastic restrictions showed the most distinct lockdown impacts. Increased particle light absorption in at the beginning of the lockdown, confirmed by assimilated satellite and remote sensing data, suggests residential combustion was the dominant BC source. Accordingly, in Central and Eastern Europe, which experienced lower than average temperatures, BC was elevated compared to the previous five years. Except for the comparison of BC emissions in the lockdown with the previous five years, an immediate decrease was also seen, as compared with the period before the lockdown, which averaged about 10 % over Europe. Such a decrease was not seen in the previous years, which also confirms an impact on BC emissions from COVID-19. [ABSTRACT FROM AUTHOR]

In order to assess the global evolution of aerosol parameters affecting climate change, a long-term trend analyses of aerosol optical properties were performed on time series from 52 stations situated across five continents. The time series of measured scattering, backscattering and absorption coefficients as well as the derived single scattering albedo, backscattering fraction, scattering and absorption Ångström exponents covered at least 10 years and up to 40 years for some stations. The non-parametric seasonal Mann-Kendall (MK) statistical test associated with several prewhitening methods and with the Sen's slope were used as main trend analysis methods. Comparisons with General Least Mean Square associated with Autoregressive Bootstrap (GLS/ARB) and with standard Least Mean Square analysis (LMS) enabled confirmation of the detected MK statistically significant trends and the assessment of advantages and limitations of each method. Currently, scattering and backscattering coefficients trends are mostly decreasing in Europe and North America and are not statistically significant in Asia, while polar stations exhibit a mix of increasing and decreasing trends. A few increasing trends are also found at some stations in North America and Australia. Absorption coefficients time series also exhibit primarily decreasing trends. For single scattering albedo, 52 % of the sites exhibit statistically significant positive trends, mostly in Asia, Eastern/Northern Europe and Arctic, 18 % of sites exhibit statistically significant negative trends, mostly in central Europe and central North America, while the remaining 30 % of sites have trends, which are not statistically significant. In addition to evaluating trends for the overall time series, the evolution of the trends in sequential 10 year segments was also analyzed. For scattering and backscattering, statistically significant increasing 10 year trends are primarily found for earlier periods (10 year trends ending in 2010-2015) for polar stations and Mauna Loa. For most of the stations, the present-day statistically significant decreasing 10 year trends of the single scattering albedo were preceded by not statistically significant and statistically significant increasing 10 year trends. The effect of air pollution abatement policies in continental North America is very obvious in the 10 year trends of the scattering coefficient - there is a shift to statistically significant negative trends in 2010-2011 for all stations in the eastern and central US. This long-term trend analysis of aerosol radiative properties with a broad spatial coverage enables a better global view of potential aerosol effects on climate changes. [ABSTRACT FROM AUTHOR]