Simulated lidar return from a one-dimensional stratospheric aerosol model

Nature ◽  
1979 ◽  
Vol 278 (5700) ◽  
pp. 149-152 ◽  
Author(s):  
PATRICK HAMILL ◽  
T. J. SWISSLER ◽  
R. P. TURCO ◽  
O. B. TOON
Keyword(s):  
Stratospheric Aerosol ◽  
One Dimensional ◽  
Aerosol Model ◽  
Lidar Return

scholarly journals Improved tropospheric and stratospheric sulfur cycle in the aerosol–chemistry–climate model SOCOL-AERv2

2019 ◽  
Vol 12 (9) ◽  
pp. 3863-3887 ◽  
Author(s):  
Aryeh Feinberg ◽  
Timofei Sukhodolov ◽  
Bei-Ping Luo ◽  
Eugene Rozanov ◽  
Lenny H. E. Winkel ◽  
...  
Keyword(s):  
Climate Model ◽  
Model Performance ◽  
Stratospheric Aerosol ◽  
Sulfur Cycle ◽  
Sulfate Aerosol ◽  
Tropospheric Chemistry ◽  
Sulfur Deposition ◽  
Aerosol Chemistry ◽  
Deposition Fluxes ◽  
Aerosol Model

Abstract. SOCOL-AERv1 was developed as an aerosol–chemistry–climate model to study the stratospheric sulfur cycle and its influence on climate and the ozone layer. It includes a sectional aerosol model that tracks the sulfate particle size distribution in 40 size bins, between 0.39 nm and 3.2 µm. Sheng et al. (2015) showed that SOCOL-AERv1 successfully matched observable quantities related to stratospheric aerosol. In the meantime, SOCOL-AER has undergone significant improvements and more observational datasets have become available. In producing SOCOL-AERv2 we have implemented several updates to the model: adding interactive deposition schemes, improving the sulfate mass and particle number conservation, and expanding the tropospheric chemistry scheme. We compare the two versions of the model with background stratospheric sulfate aerosol observations, stratospheric aerosol evolution after Pinatubo, and ground-based sulfur deposition networks. SOCOL-AERv2 shows similar levels of agreement as SOCOL-AERv1 with satellite-measured extinctions and in situ optical particle counter (OPC) balloon flights. The volcanically quiescent total stratospheric aerosol burden simulated in SOCOL-AERv2 has increased from 109 Gg of sulfur (S) to 160 Gg S, matching the newly available satellite estimate of 165 Gg S. However, SOCOL-AERv2 simulates too high cross-tropopause transport of tropospheric SO2 and/or sulfate aerosol, leading to an overestimation of lower stratospheric aerosol. Due to the current lack of upper tropospheric SO2 measurements and the neglect of organic aerosol in the model, the lower stratospheric bias of SOCOL-AERv2 was not further improved. Model performance under volcanically perturbed conditions has also undergone some changes, resulting in a slightly shorter volcanic aerosol lifetime after the Pinatubo eruption. With the improved deposition schemes of SOCOL-AERv2, simulated sulfur wet deposition fluxes are within a factor of 2 of measured deposition fluxes at 78 % of the measurement stations globally, an agreement which is on par with previous model intercomparison studies. Because of these improvements, SOCOL-AERv2 will be better suited to studying changes in atmospheric sulfur deposition due to variations in climate and emissions.

scholarly journals Simulation of ash clouds after a Laacher See-type eruption

2021 ◽  
Author(s):  
Ulrike Niemeier ◽  
Felix Riede ◽  
Claudia Timmreck
Keyword(s):  
Explosive Volcanism ◽  
Stratospheric Aerosol ◽  
Radiative Heating ◽  
The Arctic ◽  
Current Evidence ◽  
Aerosol Model ◽  
Model Experiments ◽  
North East ◽  
Volcanic Cloud ◽  
The Impact

<p>The large explosive eruption of the Laacher See volcano c. 12,900 yrs BP marked the end of explosive volcanism in the East Eifel volcanic zone (Germany). We have reviewed the current evidence for the impact of the Laacher See Eruption (LSE) on the immediate and wider environment as recorded in a range of proxies with a series of interactive stratospheric aerosol model experiments. Recent studies about the climate impact of NH extratropical eruptions and new insights about the dating of the LSE warrant a return to this cataclysmic eruption and its potential influence on Northern Hemisphere climate. Rather detailed reconstructions of its eruption dynamics have been proposed. The eruption might have lasted several weeks or even months, most likely with an initial (~10h) intense early phase resulting in deposits over north-east Germany and the Baltic Sea, and a slightly later and weaker phase leaving deposits south of the volcano towards the Alps.</p><p>Our interactive stratospheric aerosol model experiments are based on a reference LSE experiment with emission estimates of 20 Tg of sulfur dioxide (SO<sub>2</sub>) and 200 Tg of fine-ash, across two eruptive phases in May and June. Additional sensitivity experiments reflect the estimated range of uncertainty of the injection rate and altitude and, assess how the solar-absorptive heating from the 150 Tg of sub-micron ash emitted in the first eruptive phase changed the LSE cloud’s dispersion. Our simulations reveal that the heating of the ash likely played an important role in the transport of ash and sulfate. Depending on the altitude of the injection, our simulated volcanic cloud begins to rotate shortly after the eruption. This meso-cyclone, as well as the additional radiative heating of the fine ash then changes the dispersion of the cloud to be more southerly compared to dispersal estimated without fine-ash heating. Sulfate transport is similarly impacted by the heating of the ash, resulting in a stronger transport to low-latitudes, later arrival of the volcanic cloud in the Arctic regions and a longer lifetime compared to cases without injection of fine ash.</p>

scholarly journals The Interactive Stratospheric Aerosol Model Intercomparison Project (ISA-MIP): motivation and experimental design

2018 ◽  
Vol 11 (7) ◽  
pp. 2581-2608 ◽  
Author(s):  
Claudia Timmreck ◽  
Graham W. Mann ◽  
Valentina Aquila ◽  
Rene Hommel ◽  
Lindsay A. Lee ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Volcanic Eruptions ◽  
Stratospheric Aerosol ◽  
Transport Processes ◽  
Aerosol Layer ◽  
Model Intercomparison ◽  
Aerosol Model ◽  
Model Experiments ◽  
Aerosol Forcing ◽  
Intercomparison Project

Abstract. The Stratospheric Sulfur and its Role in Climate (SSiRC) Interactive Stratospheric Aerosol Model Intercomparison Project (ISA-MIP) explores uncertainties in the processes that connect volcanic emission of sulfur gas species and the radiative forcing associated with the resulting enhancement of the stratospheric aerosol layer. The central aim of ISA-MIP is to constrain and improve interactive stratospheric aerosol models and reduce uncertainties in the stratospheric aerosol forcing by comparing results of standardized model experiments with a range of observations. In this paper we present four co-ordinated inter-model experiments designed to investigate key processes which influence the formation and temporal development of stratospheric aerosol in different time periods of the observational record. The Background (BG) experiment will focus on microphysics and transport processes under volcanically quiescent conditions, when the stratospheric aerosol is controlled by the transport of aerosols and their precursors from the troposphere to the stratosphere. The Transient Aerosol Record (TAR) experiment will explore the role of small- to moderate-magnitude volcanic eruptions, anthropogenic sulfur emissions, and transport processes over the period 1998–2012 and their role in the warming hiatus. Two further experiments will investigate the stratospheric sulfate aerosol evolution after major volcanic eruptions. The Historical Eruptions SO2 Emission Assessment (HErSEA) experiment will focus on the uncertainty in the initial emission of recent large-magnitude volcanic eruptions, while the Pinatubo Emulation in Multiple models (PoEMS) experiment will provide a comprehensive uncertainty analysis of the radiative forcing from the 1991 Mt Pinatubo eruption.

Volcanic forcing of climate since 1850 in an interactive aerosol-chemistry-climate model

2021 ◽  
Author(s):  
Thomas Aubry ◽  
Anja Schmidt ◽  
Alix Harrow ◽  
Jeremy Walton ◽  
Jane Mulcahy ◽  
...  
Keyword(s):  
Optical Properties ◽  
Radiative Forcing ◽  
Climate Models ◽  
Climate Model ◽  
Coupled Model ◽  
Ice Cores ◽  
Volcanic Eruptions ◽  
Stratospheric Aerosol ◽  
Aerosol Model ◽  
Volcanic Forcing

<p>Reconstructions of volcanic aerosol forcing and its climatic impacts are undermined by uncertainties in both the models used to build these reconstructions as well as the proxy and observational records used to constrain those models. Reducing these uncertainties has been a priority and in particular, several modelling groups have developed interactive stratospheric aerosol models. Provided with an initial volcanic injection of sulfur dioxide, these models can interactively simulate the life cycle and optical properties of sulfate aerosols, and their effects on climate. In contrast, most climate models that took part in the Coupled Model Intercomparison Project Phase 5 and 6 (CMIP6) directly prescribe perturbations in atmospheric optical properties associated with an eruption. However, before the satellite era, the volcanic forcing dataset used for CMIP6 mostly relies on a relatively simple aerosol model and a volcanic sulfur inventory derived from ice-cores, both of which have substantial associated uncertainties.</p><p>In this study, we produced a new set of historical simulations using the UK Earth System Model UKESM1, with interactive stratospheric aerosol capability (referred to as interactive runs hereafter) instead of directly prescribing the CMIP6 volcanic forcing dataset as was done for CMIP6 (standard runs, hereafter). We used one of the most recent volcanic sulfur inventories as input for the interactive runs, in which aerosol properties are consistent with the model chemistry, microphysics and atmospheric components. We analyzed how the stratospheric aerosol optical depth, the radiative forcing and the climate response to volcanic eruptions differed between interactive and standard runs, and how these compare to observations and proxy records. In particular, we investigate in detail the differences in the response to the large-magnitude Krakatoa 1883 eruption between the two sets of runs. We also discuss differences for the 1979-2015 period where the forcing data in standard runs is directly constrained from satellite observations. Our results shed new light on uncertainties affecting the reconstruction of past volcanic forcing and highlight some of the benefits and disadvantages of using interactive stratospheric aerosol capabilities instead of a unique prescribed volcanic forcing dataset in CMIP’s historical runs.</p>

scholarly journals Improvement of stratospheric aerosol extinction retrieval from OMPS/LP using a new aerosol model

2018 ◽  
Vol 11 (12) ◽  
pp. 6495-6509 ◽  
Author(s):  
Zhong Chen ◽  
Pawan K. Bhartia ◽  
Robert Loughman ◽  
Peter Colarco ◽  
Matthew DeLand
Keyword(s):  
Size Distribution ◽  
Gamma Function ◽  
Spectral Dependence ◽  
Stratospheric Aerosol ◽  
Cumulative Distribution ◽  
Aerosol Size Distribution ◽  
Retrieval Algorithm ◽  
Aerosol Extinction ◽  
Aerosol Model ◽  
The Impact

Abstract. The Ozone Mapping and Profiler Suite Limb Profiler (OMPS/LP) has been flying on the Suomi National Polar-orbiting Partnership (S-NPP) satellite since October 2011. It is designed to produce ozone and aerosol vertical profiles at ∼2 km vertical resolution over the entire sunlit globe. Aerosol extinction profiles are computed with Mie theory using radiances measured at 675 nm. The operational Version 1.0 (V1.0) aerosol extinction retrieval algorithm assumes a bimodal lognormal aerosol size distribution (ASD) whose parameters were derived by combining an in situ measurement of aerosol microphysics with the Stratospheric Aerosol and Gas Experiment (SAGE II) aerosol extinction climatology. Internal analysis indicates that this bimodal lognormal ASD does not sufficiently explain the spectral dependence of LP-measured radiances. In this paper we describe the derivation of an improved aerosol size distribution, designated Version 1.5 (V1.5), for the LP retrieval algorithm. The new ASD uses a gamma function distribution that is derived from Community Aerosol and Radiation Model for Atmospheres (CARMA)-calculated results. A cumulative distribution fit derived from the gamma function ASD gives better agreement with CARMA results at small particle radii than bimodal or unimodal functions. The new ASD also explains the spectral dependence of LP-measured radiances better than the V1.0 ASD. We find that the impact of our choice of ASD on the retrieved extinctions varies strongly with the underlying reflectivity of the scene. Initial comparisons with collocated extinction profiles retrieved at 676 nm from the SAGE III instrument on the International Space Station (ISS) show a significant improvement in agreement for the LP V1.5 retrievals. Zonal mean extinction profiles agree to within 10  % between 19 and 29 km, and regression fits of collocated samples show improved correlation and reduced scatter compared to the V1.0 product. This improved agreement will motivate development of more sophisticated ASDs from CARMA results that incorporate latitude, altitude and seasonal variations in aerosol properties.

scholarly journals The Interactive Stratospheric Aerosol Model Intercomparison Project (ISA-MIP): Motivation and experimental design

2018 ◽  
Author(s):  
Claudia Timmreck ◽  
Graham W. Mann ◽  
Valentina Aquila ◽  
Rene Hommel ◽  
Lindsay A. Lee ◽  
...  
Keyword(s):  
Radiative Forcing ◽  
Volcanic Eruptions ◽  
Stratospheric Aerosol ◽  
Transport Processes ◽  
Aerosol Layer ◽  
Model Intercomparison ◽  
Aerosol Model ◽  
Model Experiments ◽  
Aerosol Forcing ◽  
Intercomparison Project

Abstract. The Stratospheric Sulfur and its Role in Climate (SSiRC) interactive stratospheric aerosol model intercomparison project (ISA-MIP) explores uncertainties in the processes that connect volcanic emission of sulphur gas species and the radiative forcing associated with the resulting enhancement of the stratospheric aerosol layer. The central aim of ISA-MIP is to constrain and improve interactive stratospheric aerosol models and reduce uncertainties in the stratospheric aerosol forcing by comparing results of standardized model experiments with a range of observations. In this paper we present 4 co-ordinated inter-model experiments designed to investigate key processes which influence the formation and temporal development of stratospheric aerosol in different time periods of the observational record. The Background (BG) experiment will focus on microphysics and transport processes under volcanically quiescent conditions, when the stratospheric aerosol is controlled by the transport of aerosols and their precursors from the troposphere to the stratosphere. The Transient Aerosol Record (TAR) experiment will explore the role of small- to moderate-magnitude volcanic eruptions, anthropogenic sulphur emissions and transport processes over the period 1998–2012 and their role in the warming hiatus. Two further experiments will investigate the stratospheric sulphate aerosol evolution after major volcanic eruptions. The Historical Eruptions SO2 Emission Assessment (HErSEA) experiment will focus on the uncertainty in the initial emission of recent large-magnitude volcanic eruptions, while the Pinatubo Emulation in Multiple models (PoEMS) experiment will provide a comprehensive uncertainty analysis of the radiative forcing from the 1991 Mt. Pinatubo eruption.

scholarly journals Recovery of the first ever multi-year lidar dataset of the stratospheric aerosol layer, from Lexington, MA, and Fairbanks, AK, January 1964 to July 1965

2021 ◽  
Vol 13 (9) ◽  
pp. 4407-4423
Author(s):  
Juan-Carlos Antuña-Marrero ◽  
Graham W. Mann ◽  
John Barnes ◽  
Albeht Rodríguez-Vega ◽  
Sarah Shallcross ◽  
...  
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Coupled Model ◽  
Stratospheric Aerosol ◽  
Aerosol Layer ◽  
Large Variability ◽  
Aerosol Model ◽  
Intercomparison Project ◽  
Relative Errors ◽  
The Tropics

Abstract. We report the recovery and processing methodology of the first ever multi-year lidar dataset of the stratospheric aerosol layer. A Q-switched ruby lidar measured 66 vertical profiles of 694 nm attenuated backscatter at Lexington, Massachusetts, between January 1964 and August 1965, with an additional nine profile measurements conducted from College, Alaska, during July and August 1964. We describe the processing of the recovered lidar backscattering ratio profiles to produce mid-visible (532 nm) stratospheric aerosol extinction profiles (sAEP532) and stratospheric aerosol optical depth (sAOD532) measurements, utilizing a number of contemporary measurements of several different atmospheric variables. Stratospheric soundings of temperature and pressure generate an accurate local molecular backscattering profile, with nearby ozone soundings determining the ozone absorption, which are used to correct for two-way ozone transmittance. Two-way aerosol transmittance corrections are also applied based on nearby observations of total aerosol optical depth (across the troposphere and stratosphere) from sun photometer measurements. We show that accounting for these two-way transmittance effects substantially increases the magnitude of the 1964/1965 stratospheric aerosol layer's optical thickness in the Northern Hemisphere mid-latitudes, then ∼ 50 % larger than represented in the Coupled Model Intercomparison Project 6 (CMIP6) volcanic forcing dataset. Compared to the uncorrected dataset, the combined transmittance correction increases the sAOD532 by up to 66 % for Lexington and up to 27 % for Fairbanks, as well as individual sAEP532 adjustments of similar magnitude. Comparisons with the few contemporary measurements available show better agreement with the corrected two-way transmittance values. Within the January 1964 to August 1965 measurement time span, the corrected Lexington sAOD532 time series is substantially above 0.05 in three distinct periods, October 1964, March 1965, and May–June 1965, whereas the 6 nights the lidar measured in December 1964 and January 1965 had sAOD values of at most ∼ 0.03. The comparison with interactive stratospheric aerosol model simulations of the Agung aerosol cloud shows that, although substantial variation in mid-latitude sAOD532 are expected from the seasonal cycle in the stratospheric circulation, the Agung cloud's dispersion from the tropics would have been at its strongest in winter and weakest in summer. The increasing trend in sAOD from January to July 1965, also considering the large variability, suggests that the observed variations are from a different source than Agung, possibly from one or both of the two eruptions that occurred in 1964/1965 with a Volcanic Explosivity Index (VEI) of 3: Trident, Alaska, and Vestmannaeyjar, Heimaey, south of Iceland. A detailed error analysis of the uncertainties in each of the variables involved in the processing chain was conducted. Relative errors for the uncorrected sAEP532 were 54 % for Fairbanks and 44 % Lexington. For the corrected sAEP532 the errors were 61 % and 64 %, respectively. The analysis of the uncertainties identified variables that with additional data recovery and reprocessing could reduce these relative error levels. Data described in this work are available at https://doi.org/10.1594/PANGAEA.922105 (Antuña-Marrero et al., 2020a).

scholarly journals Improvement of stratospheric aerosol extinction retrieval from OMPS/LP using a new aerosol model

2018 ◽  
Author(s):  
Zhong Chen ◽  
Pawan K. Bhartia ◽  
Robert Loughman ◽  
Peter Colarco ◽  
Matthew DeLand
Keyword(s):  
Size Distribution ◽  
Gamma Function ◽  
Spectral Dependence ◽  
Stratospheric Aerosol ◽  
Cumulative Distribution ◽  
Aerosol Size Distribution ◽  
Retrieval Algorithm ◽  
Aerosol Extinction ◽  
Aerosol Model ◽  
The Impact

Abstract. The Ozone Mapping and Profiler Suite Limb Profiler (OMPS/LP) has been flying on the Suomi NPP satellite since October 2011. It is designed to produce ozone and aerosol vertical profiles at ~2 km vertical resolution over the entire sunlit globe. Aerosol extinction profiles are computed with Mie theory using radiances measured at 675 nm. The operational Version 1.0 (V1.0) aerosol extinction retrieval algorithm assumes a bimodal lognormal aerosol size distribution (ASD) whose parameters were derived by combining an in situ measurement of aerosol microphysics with the SAGE II aerosol extinction climatology. Internal analysis indicates that this bimodal lognormal ASD does not sufficiently explain the spectral dependence of LP measured radiances. In this paper we describe the derivation of an improved aerosol size distribution, designated Version 1.5 (V1.5), for the LP retrieval algorithm. The new ASD uses a gamma function distribution that is derived from Community Aerosol and Radiation Model for Atmospheres (CARMA) calculated results. A cumulative distribution fit derived from the gamma function ASD gives better agreement with CARMA results at small particle radii than bimodal or unimodal functions. The new ASD also explains the spectral dependence of LP measured radiances better than the V1.0 ASD. We find that the impact of our choice of ASD on the retrieved extinctions varies strongly with the underlying reflectivity of the scene. Initial comparisons with co-located extinction profiles retrieved at 676 nm from the SAGE III/ISS instrument show a significant improvement in agreement for the LP V1.5 retrievals. Zonal mean extinction profiles agree to within 10 % between 19–29 km, and regression fits of collocated samples show improved correlation and reduced scatter compared to the V1.0 product. This improved agreement will motivate development of more sophisticated ASDs from CARMA results that incorporate latitude, altitude, and seasonal variations in aerosol properties.

scholarly journals Evaluating the simulated radiative forcings, aerosol properties and stratospheric warmings from the 1963 Agung, 1982 El Chichón and 1991 Mt Pinatubo volcanic aerosol clouds

2020 ◽  
Author(s):  
Sandip S. Dhomse ◽  
Graham W. Mann ◽  
Juan Carlos Antuña Marrero ◽  
Sarah E. Shallcross ◽  
Martyn P. Chipperfield ◽  
...  
Keyword(s):  
Volcanic Eruptions ◽  
Stratospheric Aerosol ◽  
Volcanic Aerosol ◽  
Model Intercomparison ◽  
Tropical Reservoir ◽  
So2 Emission ◽  
Aerosol Model ◽  
Volcanic Forcing ◽  
El Chichón ◽  
El Chichon

Abstract. Accurate quantification of the effects of volcanic eruptions on climate is a key requirement for better attribution of anthropogenic climate change. Here we use the UM-UKCA composition-climate model to simulate the atmospheric evolution of the volcanic aerosol clouds from the three largest eruptions of the 20th century: 1963 Agung, 1982 El Chichón and 1991 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 3-member ensemble model experiments with upper, mid-point and lower estimates for SO2 emission, each initialised to a meteorological state to match the observed phase of the quasi-biennial oscillation (QBO) at the times of the eruptions. We assess how each eruption's emitted SO2 evolves into a tropical reservoir of volcanic aerosol and analyse the subsequent dispersion to mid-latitudes. We compare the simulations to the three volcanic forcing datasets used in historical integrations for the two most recent Coupled Model Intercomparison Project (CMIP) assessments: the Global Space-based Stratospheric Aerosol Climatology (GloSSAC) for CMIP6, and the Sato et al. (1993) and Ammann et al. (2003) datasets used in CMIP5. We also assess the vertical extent of the volcanic aerosol clouds by comparing simulated extinction to Stratospheric Aerosol and Gas Experiment II (SAGE-II) v7.0 satellite aerosol data (1985–1995) for Pinatubo and El Chichón, and to 1964–65 northern hemisphere ground-based lidar measurements for Agung. As an independent test for the simulated volcanic forcing after Pinatubo, we also compare to the shortwave (SW) and longwave (LW) Top-of-the-Atmosphere 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 sulphur burden, with good agreement also to SAGE-II mid-visible and near-infrared extinction measurements. This 10–14 Tg range of emission also generates a heating of the tropical stratosphere that is comparable with the temperature anomaly seen in the ERA-Interim reanalyses. For El Chichón the simulations with 5 Tg and 7 Tg SO2 emission give best agreement with the observations. However, these runs predict a much deeper volcanic cloud than present in the CMIP6 data, with much higher aerosol extinction than the GloSSAC data up to October 1984, but better agreement during the later SAGE-II period. For 1963 Agung, the 9 Tg simulation compares best to the forcing datasets with the model capturing the lidar-observed signature of peak extinction descending from 20 km in 1964 to 16 km in 1965. Overall, our results indicate that the downward adjustment to previous SO2 emission estimates for Pinatubo as suggested by several interactive modelling studies is also needed for the Agung and El Chichón aerosol clouds. This strengthens the hypothesis that interactive stratospheric aerosol models may be missing an important removal or redistribution 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 analysis identifies potentially important inhomogeneities in the CMIP6 dataset for all three periods that are hard to reconcile with variations predicted by the interactive stratospheric aerosol model. 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.

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