Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space-based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long-term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfate matter such as black carbon and organics. Chemistry-climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.

Abstract. Accurately quantifying volcanic impacts on climate is a key requirement for robust attribution of anthropogenic climate change. Here we use the Unified Model – United Kingdom Chemistry and Aerosol (UM-UKCA) composition–climate model to simulate the global dispersion of the volcanic aerosol clouds from the three largest eruptions of the 20th century: 1963 Mt Agung, 1982 El Chichón, and 1991 Mt Pinatubo. The model has interactive stratospheric chemistry and aerosol microphysics, with coupled aerosol–radiation interactions for realistic composition–dynamics feedbacks. Our simulations align with the design of the Interactive Stratospheric Aerosol Model Intercomparison (ISA-MIP) “Historical Eruption SO2 Emissions Assessment”. For each eruption, we perform three-member ensemble model experiments for upper, mid-point, and lower estimates of SO2 emission, each re-initialised from a control run to approximately match the observed transition in the phase of the quasi-biennial oscillation (QBO) in the 6 months after the eruptions. With this experimental design, we assess how each eruption's emitted SO2 translates into a tropical reservoir of volcanic aerosol and analyse the subsequent dispersion to mid-latitudes. We compare the simulations to the volcanic forcing datasets (e.g. Space-based Stratospheric Aerosol Climatology (GloSSAC); Sato et al., 1993, and Ammann et al., 2003) that are used in historical integrations for the two most recent Coupled Model Intercomparison Project (CMIP) assessments. For Pinatubo and El Chichón, we assess the vertical extent of the simulated volcanic clouds by comparing modelled extinction to the Stratospheric Aerosol and Gas Experiment (SAGE-II) v7.0 satellite measurements and to 1964–1965 Northern Hemisphere ground-based lidar measurements for Agung. As an independent test for the simulated volcanic forcing after Pinatubo, we also compare simulated shortwave (SW) and longwave (LW) top-of-the-atmosphere radiative forcings to the flux anomalies measured by the Earth Radiation Budget Experiment (ERBE) satellite instrument. For the Pinatubo simulations, an injection of 10 to 14 Tg SO2 gives the best match to the High Resolution Infrared Sounder (HIRS) satellite-derived global stratospheric sulfur burden, with good agreement also with SAGE-II mid-visible and near-infra-red extinction measurements. This 10–14 Tg range of emission also generates a heating of the tropical stratosphere that is consistent with the temperature anomaly present in the ERA-Interim reanalysis. For El Chichón, the simulations with 5 and 7 Tg SO2 emission give best agreement with the observations. However, these simulations predict a much deeper volcanic cloud than represented in the GloSSAC dataset, which is largely based on an interpolation between Stratospheric Aerosol Measurements (SAM-II) satellite and aircraft measurements. In contrast, these simulations show much better agreement during the SAGE-II period after October 1984. For 1963 Agung, the 9 Tg simulation compares best to the forcing datasets with the model capturing the lidar-observed signature of the altitude of peak extinction descending from 20 km in 1964 to 16 km in 1965. Overall, our results indicate that the downward adjustment to SO2 emission found to be required by several interactive modelling studies when simulating Pinatubo is also needed when simulating the Agung and El Chichón aerosol clouds. This strengthens the hypothesis that interactive stratospheric aerosol models may be missing an important removal or re-distribution process (e.g. effects of co-emitted ash) which changes how the tropical reservoir of volcanic aerosol evolves in the initial months after an eruption. Our model comparisons also identify potentially important inhomogeneities in the CMIP6 dataset for all three eruption periods that are hard to reconcile with variations predicted in the interactive stratospheric aerosol simulations. We also highlight large differences between the CMIP5 and CMIP6 volcanic aerosol datasets for the Agung and El Chichón periods. Future research should aim to reduce this uncertainty by reconciling the datasets with additional stratospheric aerosol observations.

Sustained and coordinated efforts of lidar teams in Latin America at the beginning of the twenty-first century have built the Latin American Lidar Network (LALINET), the only observational network in Latin America created by the agreement and commitment of Latin American scientists. They worked with limited funding but an abundance of enthusiasm and commitment toward their joint goal. Before LALINET, there were a few pioneering lidar stations operating in Latin America, described briefly here. Biannual Latin American lidar workshops, held from 2001 to the present, supported both the development of the regional lidar community and LALINET. At those meetings, lidar researchers from Latin America met to conduct regular scientific and technical exchanges among themselves and with experts from the rest of the world. Regional and international scientific cooperation has played an important role in the development of both the individual teams and the network. The current LALINET status and activities are described, emphasizing the processes of standardization of the measurements, methodologies, calibration protocols, and retrieval algorithms. Failures and successes achieved in the buildup of LALINET are presented. In addition, the first LALINET joint measurement campaign and a set of aerosol extinction profile measurements obtained from the aerosol plume produced by the Calbuco volcano eruption on 22 April 2015 are described and discussed.

On 22 April 2015, the Calbuco volcano in Chile (Lat: 41.33 ∘ S, Long: 72.62 ∘ W) erupted after 43 years of inactivity followed by a great amount of aerosol injection into the atmosphere. The pyroclastic material dispersed into the atmosphere posed a potential threat to aviation traffic and air quality over affected a large area. The plumes and debris spread from its location to Patagonian and Pampean regions, reaching the Atlantic and Pacific Oceans and neighboring countries, such as Argentina, Brazil and Uruguay, driven by the westerly winds at these latitudes. The presence of volcanic aerosol layers could be identified promptly at the proximities of Calbuco and afterwards by remote sensing using satellites and lidars in the path of the dispersed aerosols. The Cloud-Aerosol Lidar and Pathfinder Satellite Observations (CALIPSO), Moderate Resolution Imaging Spectroradiometer (MODIS) on board of AQUA/TERRA satellites and Ozone Mapping and Profiler Suite (OMPS) on board of Suomi National Polar-orbiting Partnership (Suomi NPP) satellite were the space platforms used to track the injected layers and a multi-channel lidar system from Latin America Lidar Network (LALINET) SPU Lidar station in South America allowed us to get the spatial and temporal distribution of Calbuco ashes after its occurrence. The SPU lidar stations co-located Aerosol Robotic Network (AERONET) sunphotometers to help in the optical characterization. Here, we present the volcanic layer transported over São Paulo area and the detection of aerosol plume between 18 and 20 km. The path traveled by the volcanic aerosol to reach the Metropolitan Area of São Paulo (MASP) was tracked by CALIPSO and the aerosol optical and geometrical properties were retrieved at some points to monitor the plume evolution. Total attenuated backscatter profile at 532 nm obtained by CALIPSO revealed the height range extension of the aerosol plume between 18 and 20 km and are in agreement with SPU lidar range corrected signal at 532 nm. The daily evolution of Aerosol Optical Depth (AOD) at 532 and 355 nm, retrieved from AERONET sunphotometer, showed a substantial increasing on 27 April, the day of the volcanic plume detection at Metropolitan Area of São Paulo (MASP), achieving values of 0 . 33 ± 0 . 16 and 0 . 22 ± 0 . 09 at 355 and 532 nm, respectively. AERONET aerosol size distribution was dominated by fine mode aerosol over coarse mode, especially on 27 and 28 April. The space and time coincident aerosol extinction profiles from SPU lidar station and OMPS LP from the Calbuco eruption conducted on 27 April agreed on the double layer structure. The main objective of this study was the application of the transmittance method, using the Platt formalism, to calculate the optical and physical properties of volcanic plume, i.e., aerosol bottom and top altitude, the aerosol optical depth and lidar ratio. The aerosol plume was detected between 18 and 19.3 km, with AOD value of 0.159 at 532 nm and Ånsgtröm exponent of 0 . 61 ± 0 . 58 . The lidar ratio retrieved was 76 ± 27 sr and 63 ± 21 sr at 532 and 355 nm, respectively. Considering the values of these parameters, the Calbuco volcanic aerosol layers could be classified as sulfates with some ash type.

This paper provides early instrumental data recovered for 20 countries of Latin-America and the Caribbean (Argentina, Bahamas, Belize, Brazil, British Guiana, Chile, Colombia, Costa Rica, Cuba, Ecuador, France (Martinique and Guadalupe), Guatemala, Jamaica, Mexico, Nicaragua, Panama, Peru, Puerto Rico, El Salvador and Suriname) during the 18th and 19th centuries. The main meteorological variables retrieved were air temperature, atmospheric pressure, and precipitation, but other variables, such as humidity, wind direction, and state of the sky were retrieved when possible. In total, more than 300,000 early instrumental data were rescued (96% with daily resolution). Especial effort was made to document all the available metadata in order to allow further post-processing. The compilation is far from being exhaustive, but the dataset will contribute to a better understanding of climate variability in the region, and to enlarging the period of overlap between instrumental data and natural/documentary proxies.