Understanding the cooling effect of recent volcanoes is of particular interest in the context of the post-2000 slowing of the rate of global warming. Satellite observations of aerosol optical depth above 15 km have demonstrated that small-magnitude volcanic eruptions substantially perturb incoming solar radiation. Here we use lidar, Aerosol Robotic Network, and balloon-borne observations to provide evidence that currently available satellite databases neglect substantial amounts of volcanic aerosol between the tropopause and 15 km at middle to high latitudes and therefore underestimate total radiative forcing resulting from the recent eruptions. Incorporating these estimates into a simple climate model, we determine the global volcanic aerosol forcing since 2000 to be À0.19 ± 0.09 Wm À2 . This translates into an estimated global cooling of 0.05 to 0.12°C. We conclude that recent volcanic events are responsible for more post-2000 cooling than is implied by satellite databases that neglect volcanic aerosol effects below 15 km.

An analytical inversion method is used to estimate the vertical profile of sulfur dioxide (SO2) emissions from the major 2008 eruption of Kasatochi Volcano, located on the Aleutian Arc, Alaska. The method uses satellite‐observed total SO2 columns from the Global Ozone Monitoring Experiment‐2 (GOME‐2), Ozone Monitoring Instrument (OMI), and Atmospheric InfraRed Sounder (AIRS) during the first 2 days after the eruption, and an atmospheric transport model, FLEXPART, to calculate the vertical emission profile. The inversion yields an emission profile with two large emission maxima near 7 km above sea level (asl) and around 12 km asl, with smaller emissions up to 20 km. The total mass of SO2 injected into the atmosphere by the eruption is estimated to 1.7 Tg, with ∼1 Tg reaching the stratosphere (above 10 km asl). The estimated vertical emission profile is robust against changes of the assumed eruption time, meteorological input data, and satellite data used. Using the vertical emission profile, a simulation of the transport extending for 1 month after the eruption is performed. The simulated cloud agrees very well with SO2 columns observed by GOME‐2, OMI, and AIRS until 6 days after the eruption, and the altitudes agree with both Cloud‐Aerosol Lidar and Infrared Pathfinder Satellite Observation measurements and ground‐based lidar observations to within 1 km. The method is computationally very fast. It is therefore suitable for implementation within an operational environment, such as the Volcanic Ash Advisory Centers, to predict the threat posed by volcanic emissions for air traffic.

Abstract. During the 1-year MOSAiC (Multidisciplinary drifting Observatory for the Study of Arctic Climate) expedition, the German icebreaker Polarstern drifted through Arctic Ocean ice from October 2019 to May 2020, mainly at latitudes between 85 and 88.5∘ N. A multiwavelength polarization Raman lidar was operated on board the research vessel and continuously monitored aerosol and cloud layers up to a height of 30 km. During our mission, we expected to observe a thin residual volcanic aerosol layer in the stratosphere, originating from the Raikoke volcanic eruption in June 2019, with an aerosol optical thickness (AOT) of 0.005–0.01 at 500 nm over the North Pole area during the winter season. However, the highlight of our measurements was the detection of a persistent, 10 km deep aerosol layer in the upper troposphere and lower stratosphere (UTLS), from about 7–8 to 17–18 km height, with clear and unambiguous wildfire smoke signatures up to 12 km and an order of magnitude higher AOT of around 0.1 in the autumn of 2019. Case studies are presented to explain the specific optical fingerprints of aged wildfire smoke in detail. The pronounced aerosol layer was present throughout the winter half-year until the strong polar vortex began to collapse in late April 2020. We hypothesize that the detected smoke originated from extraordinarily intense and long-lasting wildfires in central and eastern Siberia in July and August 2019 and may have reached the tropopause layer by the self-lifting process. In this article, we summarize the main findings of our 7-month smoke observations and characterize the aerosol in terms of geometrical, optical, and microphysical properties. The UTLS AOT at 532 nm ranged from 0.05–0.12 in October–November 2019 and 0.03–0.06 during the main winter season. The Raikoke aerosol fraction was estimated to always be lower than 15 %. We assume that the volcanic aerosol was above the smoke layer (above 13 km height). As an unambiguous sign of the dominance of smoke in the main aerosol layer from 7–13 km height, the particle extinction-to-backscatter ratio (lidar ratio) at 355 nm was found to be much lower than at 532 nm, with mean values of 55 and 85 sr, respectively. The 355–532 nm Ångström exponent of around 0.65 also clearly indicated the presence of smoke aerosol. For the first time, we show a distinct view of the aerosol layering features in the High Arctic from the surface up to 30 km height during the winter half-year. Finally, we provide a vertically resolved view on the late winter and early spring conditions regarding ozone depletion, smoke occurrence, and polar stratospheric cloud formation. The latter will largely stimulate research on a potential impact of the unexpected stratospheric aerosol perturbation on the record-breaking ozone depletion in the Arctic in spring 2020.

[1] We present particle effective radii and Å ngström exponents of aged free-tropospheric forest-fire smoke. The particle plumes were observed with different multiwavelength Raman lidars downwind of the fires that burned in boreal areas of the northern hemisphere. We find an increase of particle size, respectively decrease of the Å ngström exponent with transport time which was more than two weeks in some of the investigated cases. Mean effective radii were as large as 0.4 mm. Mean Å ngström exponents were as low as 0.04 for the wavelength pair at 355/532 nm. A fit curve that describes particle growth with time is derived. Particle growth levels off after approximately ten days of transport time. Citation: Müller, D., I. Mattis, A. Ansmann, U. Wandinger, C. Ritter, and D. Kaiser (2007), Multiwavelength Raman lidar observations of particle growth during long-range transport of forest-fire smoke in the free troposphere, Geophys. Res. Lett., 34, L05803,

Multi-year sets of ground-based sun-photometer measurements conducted at 12 Arctic sites and 9 Antarctic sites were examined to determine daily mean values of aerosol optical thickness () at visible and near-infrared wavelengths, from which best-fit values of Ångström"s exponent  were calculated. Analysing these data, the monthly mean values of (0.50 µm) and  and the relative frequency histograms of the daily mean values of both parameters were determined for winterspring and summer-autumn in the Arctic and for austral summer in Antarctica. The Arctic and Antarctic covariance plots of the seasonal median values of  versus (0.50 µm) showed: (i) a considerable increase in (0.50 µm) for the Arctic aerosol from summer to winter-spring, without marked changes in ; and (ii) a marked increase in (0.50 µm) passing from the Antarctic Plateau to coastal sites, whereas  decreased considerably due to the larger fraction of sea-salt aerosol. Good agreement was found when comparing ground-based sun-photometer measurements of () and  at Arctic and Antarctic coastal sites with Microtops measurements conducted during numerous AERONET/MAN cruises from 2006 to 2013 in three Arctic Ocean sectors and in coastal and offshore regions of the Southern Atlantic, Pacific, and Indian Oceans, and the Antarctic Peninsula. Lidar measurements were also examined to characterise vertical profiles of the aerosol backscattering coefficient measured throughout the year at Ny-Ålesund. Satellite-based MODIS, MISR, and AATSR retrievals of () over large parts of the oceanic polar regions during spring and summer were in close agreement with ship-borne and coastal ground-based sun-photometer measurements. An overview of the chemical composition of fine and accumulation/coarse mode particles is also presented, based on in-situ measurements at Arctic and Antarctic sites. Fourteen log-normal aerosol number size-distributions were defined to represent the average features of fine and accumulation/coarse mode particles for Arctic haze, summer background aerosol, Asian dust and boreal forest fire smoke, and for various background austral summer aerosol types at coastal 4 and high-altitude Antarctic sites. The main columnar aerosol optical characteristics were determined for all particle modes, based on in-situ measurements of the scattering and absorption coefficients. Diurnally averaged direct aerosol-induced radiative forcing and efficiency were calculated for a set of multimodal aerosol extinction models, using various Bidirectional Reflectance Distribution Function models over vegetation-covered, oceanic and snow-covered surfaces. These gave a reliable measure of the pronounced effects of aerosols on the radiation balance of the surface-atmosphere system over polar regions.