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    Ozone depletion in the Arctic and Antarctic stratosphere induced by wildfire smoke
    (Katlenburg-Lindau : EGU, 2022) Ansmann, Albert; Ohneiser, Kevin; Chudnovsky, Alexandra; Knopf, Daniel A.; Eloranta, Edwin W.; Villanueva, Diego; Seifert, Patric; Radenz, Martin; Barja, Boris; Zamorano, Félix; Jimenez, Cristofer; Engelmann, Ronny; Baars, Holger; Griesche, Hannes; Hofer, Julian; Althausen, Dietrich; Wandinger, Ulla
    A record-breaking stratospheric ozone loss was observed over the Arctic and Antarctica in 2020. Strong ozone depletion occurred over Antarctica in 2021 as well. The ozone holes developed in smoke-polluted air. In this article, the impact of Siberian and Australian wildfire smoke (dominated by organic aerosol) on the extraordinarily strong ozone reduction is discussed. The study is based on aerosol lidar observations in the North Pole region (October 2019-May 2020) and over Punta Arenas in southern Chile at 53.2°S (January 2020-November 2021) as well as on respective NDACC (Network for the Detection of Atmospheric Composition Change) ozone profile observations in the Arctic (Ny-Ålesund) and Antarctica (Neumayer and South Pole stations) in 2020 and 2021. We present a conceptual approach on how the smoke may have influenced the formation of polar stratospheric clouds (PSCs), which are of key importance in the ozone-depleting processes. The main results are as follows: (a) the direct impact of wildfire smoke below the PSC height range (at 10-12 km) on ozone reduction seems to be similar to well-known volcanic sulfate aerosol effects. At heights of 10-12 km, smoke particle surface area (SA) concentrations of 5-7 μm2 cm-3 (Antarctica, spring 2021) and 6-10 μm2 cm-3 (Arctic, spring 2020) were correlated with an ozone reduction in terms of ozone partial pressure of 0.4-1.2 mPa (about 30 % further ozone reduction over Antarctica) and of 2-3.5 mPa (Arctic, 20 %-30 % reduction with respect to the long-term springtime mean). (b) Within the PSC height range, we found indications that smoke was able to slightly increase the PSC particle number and surface area concentration. In particular, a smoke-related additional ozone loss of 1-2 mPa (10 %-20 % contribution to the total ozone loss over Antarctica) was observed in the 14-23 km PSC height range in September-October 2020 and 2021. Smoke particle number concentrations ranged from 10 to 100 cm-3 and were about a factor of 10 (in 2020) and 5 (in 2021) above the stratospheric aerosol background level. Satellite observations indicated an additional mean column ozone loss (deviation from the long-term mean) of 26-30 Dobson units (9 %-10 %, September 2020, 2021) and 52-57 Dobson units (17 %-20 %, October 2020, 2021) in the smoke-polluted latitudinal Antarctic belt from 70-80°S. Copyright:
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    The vertical aerosol type distribution above Israel – 2 years of lidar observations at the coastal city of Haifa
    (Katlenburg-Lindau : EGU, 2022) Heese, Birgit; Floutsi, Athena Augusta; Baars, Holger; Althausen, Dietrich; Hofer, Julian; Herzog, Alina; Mewes, Silke; Radenz, Martin; Schechner, Yoav Y.
    For the first time, vertically resolved long-term lidar measurements of the aerosol distribution were conducted in Haifa, Israel. The measurements were performed by a PollyXT multi-wavelength Raman and polarization lidar. The lidar was measuring continuously over a 2-year period from March 2017 to May 2019. The resulting data set is a series of manually evaluated lidar optical property profiles. To identify the aerosol types in the observed layers, a novel aerosol typing method that was developed at TROPOS is used. This method applies optimal estimation to a combination of lidar-derived intensive aerosol properties to determine the statistically most-likely contribution per aerosol component in terms of relative volume. A case study that shows several elevated aerosol layers illustrates this method and shows, for example, that coarse dust particles are observed up to 5ĝ€¯km height over Israel. From the whole data set, the seasonal distribution of the observed aerosol components over Israel is derived. Throughout all seasons, coarse spherical particles like sea salt and hygroscopically grown continental aerosol were observed. These particles originate from continental Europe and were transported over the Mediterranean Sea. Sea-salt particles were observed frequently due to the coastal site of Haifa. The highest contributions of coarse spherical particles are present in summer, autumn, and winter. During spring, mostly coarse non-spherical particles that are attributed to desert dust were observed. This is consistent with the distinct dust season in spring in Israel. An automated time-height-resolved air mass source attribution method identifies the origin of the dust in the Sahara and the Arabian deserts. Fine-mode spherical particles contribute significantly to the observed aerosol mixture during all seasons. These particles originate mainly from the industrial region at the bay of Haifa.
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    Long-term profiling of aerosol light extinction, particle mass, cloud condensation nuclei, and ice-nucleating particle concentration over Dushanbe, Tajikistan, in Central Asia
    (Katlenburg-Lindau : EGU, 2020) Hofer, Julian; Ansmann, Albert; Althausen, Dietrich; Engelmann, Ronny; Baars, Holger; Abdullaev, Sabur F.; Makhmudov, Abduvosit N.
    For the first time, continuous, vertically resolved long-term aerosol measurements were conducted with a state-of-the-art multiwavelength lidar over a Central Asian site. Such observations are urgently required in efforts to predict future climate and environmental conditions and to support spaceborne remote sensing (ground truth activities). The lidar observations were performed in the framework of the Central Asian Dust Experiment (CADEX) at Dushanbe, Tajikistan, from March 2015 to August 2016. An AERONET (AErosol RObotic NETwork) sun photometer was operated at the lidar field site. During the 18-month campaign, mixtures of continental aerosol pollution and mineral dust were frequently detected from ground to cirrus height level. Regional sources of dust and pollution as well as long-range transport of mineral dust mainly from Middle Eastern and the Saharan deserts determine the aerosol conditions over Tajikistan. In this study, we summarize our findings and present seasonally resolved statistics regarding aerosol layering (main aerosol layer depth, lofted layer occurrence); optical properties (aerosol and dust optical thicknesses at 500–532 nm, vertically resolved light-extinction coefficient at 532 nm); profiles of dust and non-dust mass concentrations and dust fraction; and profiles of particle parameters relevant for liquid water, mixed-phase cloud, and cirrus formation such as cloud condensation nuclei (CCN) and ice-nucleating particle (INP) concentrations. The main aerosol layer over Dushanbe typically reaches 4–5 km height in spring to autumn. Frequently lofted dust-containing aerosol layers were observed at heights from 5 to 10 km, indicating a sensitive potential of dust to influence cloud ice formation. Typical dust mass fractions were of the order of 60 %–80 %. A considerable fraction is thus anthropogenic pollution and biomass burning smoke. The highest aerosol pollution levels (in the relatively shallow winter boundary layer) occur during the winter months. The seasonal mean 500 nm AOT (aerosol optical thickness) ranges from 0.15 in winter to 0.36 in summer during the CADEX period (March 2015 to August 2016); DOTs (dust optical thicknesses) were usually below 0.2; seasonally mean particle extinction coefficients were of the order of 100–500 Mm−1 in the main aerosol layer during the summer half year and about 100–150 Mm−1 in winter but were mainly caused by anthropogenic haze. Accordingly, the highest dust mass concentrations occurred in the summer season (200–600 µg m−3) and the lowest during the winter months (20–50 µg m−3) in the main aerosol layer. In winter, the aerosol pollution mass concentrations were 20–50 µg m−3, while during the summer half year (spring to autumn), the mass concentration caused by urban haze and biomass burning smoke decreases to 10–20 µg m−3 in the lower troposphere. The CCN concentration levels are always controlled by aerosol pollution. The INP concentrations were found to be high enough in the middle and upper troposphere to significantly influence ice formation in mixed-phase and ice clouds during spring and summer seasons.
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    Optical properties of Central Asian aerosol relevant for spaceborne lidar applications and aerosol typing at 355 and 532nm
    (Katlenburg-Lindau : EGU, 2020) Hofer, Julian; Ansmann, Albert; Althausen, Dietrich; Engelmann, Ronny; Baars, Holger; Fomba, Khanneh Wadinga; Wandinger, Ulla; Abdullaev, Sabur F.; Makhmudov, Abduvosit N.
    For the first time, a dense data set of particle extinction-to-backscatter ratios (lidar ratios), linear depolarization ratios, and backscatter- and extinction-related Ångström exponents for a Central Asian site are presented. The observations were performed with a continuously running multiwavelength polarization Raman lidar at Dushanbe, Tajikistan, during an 18-month campaign (March 2015 to August 2016). The presented seasonally resolved observations fill an important gap in the database of aerosol optical properties used in aerosol typing efforts with spaceborne lidars and ground-based lidar networks. Lidar ratios and depolarization ratios are also basic input parameters in spaceborne lidar data analyses and in efforts to harmonize long-term observations with different space lidar systems operated at either 355 or 532 nm. As a general result, the found optical properties reflect the large range of occurring aerosol mixtures consisting of long-range-transported dust (from the Middle East and the Sahara), regional desert, soil, and salt dust, and anthropogenic pollution. The full range from highly polluted to pure dust situations could be observed. Typical dust depolarization ratios of 0.23–0.29 (355 nm) and 0.30–0.35 (532 nm) were observed. In contrast, comparably low lidar ratios were found. Dust lidar ratios at 532 nm accumulated around 35–40 sr and were even lower for regional background dust conditions (20–30 sr). Detailed correlation studies (e.g., lidar ratio vs. depolarization ratios, Ångström exponent vs. lidar ratio and vs. depolarization ratio) are presented to illuminate the complex relationships between the observed optical properties and to identify the contributions of anthropogenic haze, dust, and background aerosol to the overall aerosol mixtures found within the 18-month campaign. The observation of 532 nm lidar ratios (<25 sr) and depolarization ratios (around 15 %–20 %) in layers with very low particle extinction coefficient (<30 sr) suggests that direct emission and emission of resuspended salt dust (initially originated from numerous desiccating lakes and the Aralkum desert) have a sensitive impact on the aerosol background optical properties over Dushanbe.