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  • Meteorology and Climatology; Earth Resources and Remote Sensing  (2)
  • Toba  (1)
  • Volcanology  (1)
  • 1
    Publication Date: 2023-09-12
    Description: Supervolcano eruptions have occurred throughout Earth’s history and have major environmental impacts. These impacts are mostly associated with the attenuation of visible sunlight by stratospheric sulfate aerosols, which causes cooling and deceleration of the water cycle. Supereruptions have been assumed to cause so-called volcanic winters that act as primary evolutionary factors through ecosystem disruption and famine, however, winter conditions alone may not be sufficient to cause such disruption. Here we use Earth system model simulations to show that stratospheric sulfur emissions from the Toba supereruption 74,000 years ago caused severe stratospheric ozone loss through a radiation attenuation mechanism that only moderately depends on the emission magnitude. The Toba plume strongly inhibited oxygen photolysis, suppressing ozone formation in the tropics, where exceptionally depleted ozone conditions persisted for over a year. This effect, when combined with volcanic winter in the extra-tropics, can account for the impacts of supereruptions on ecosystems and humanity.
    Description: Stratospheric sulfur emissions from the Toba supereruption about 74,000 years ago suppressed ozone formation which caused severe tropical ozone layer depletion and enhanced solar ultraviolet radiation stress, according to Earth system model simulations.
    Description: King Abdullah University of Science and Technology (KAUST) https://doi.org/10.13039/501100004052
    Description: http://hdl.handle.net/10754/667404
    Description: https://github.com/SeregaOsipov/NASA-GISS-ModelE/releases/tag/toba_o3
    Description: https://simplex.giss.nasa.gov/snapshots/
    Keywords: ddc:551 ; Atmospheric chemistry ; Natural hazards ; Palaeoclimate ; Volcanology
    Language: English
    Type: doc-type:article
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  • 2
    Publication Date: 2019-07-13
    Description: This study evaluates model-simulated dust aerosols over North Africa and the North Atlantic from five global models that participated in the Aerosol Comparison between Observations and Models phase II model experiments. The model results are compared with satellite aerosol optical depth (AOD) data from Moderate Resolution Imaging Spectroradiometer (MODIS), Multiangle Imaging Spectroradiometer (MISR), and Sea-viewing Wide Field-of-view Sensor, dust optical depth (DOD) derived from MODIS and MISR, AOD and coarse-mode AOD (as a proxy of DOD) from ground-based Aerosol Robotic Network Sun photometer measurements, and dust vertical distributions/centroid height from Cloud Aerosol Lidar with Orthogonal Polarization and Atmospheric Infrared Sounder satellite AOD retrievals. We examine the following quantities of AOD and DOD: (1) the magnitudes over land and over ocean in our study domain, (2) the longitudinal gradient from the dust source region over North Africa to the western North Atlantic, (3) seasonal variations at different locations, and (4) the dust vertical profile shape and the AOD centroid height (altitude above or below which half of the AOD is located). The different satellite data show consistent features in most of these aspects; however, the models display large diversity in all of them, with significant differences among the models and between models and observations. By examining dust emission, removal, and mass extinction efficiency in the five models, we also find remarkable differences among the models that all contribute to the discrepancies of model-simulated dust amount and distribution. This study highlights the challenges in simulating the dust physical and optical processes, even in the best known dust environment, and stresses the need for observable quantities to constrain the model processes.
    Keywords: Meteorology and Climatology; Earth Resources and Remote Sensing
    Type: GSFC-E-DAA-TN17508 , Journal of Geophysical Research: Atmospheres; 119; 10; 6259-6277
    Format: application/pdf
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  • 3
    Publication Date: 2019-07-13
    Description: Atmospheric aerosols from anthropogenic and natural sources reach the polar regions through long-range transport and affect the local radiation balance. Such transport is, however, poorly constrained in present-day global climate models, and few multi-model evaluations of polar anthropogenic aerosol radiative forcing exist. Here we compare the aerosol optical depth (AOD) at 550 nm from simulations with 16 global aerosol models from the AeroCom Phase II model intercomparison project with available observations at both poles. We show that the annual mean multi-model median is representative of the observations in Arctic, but that the intermodel spread is large. We also document the geographical distribution and seasonal cycle of the AOD for the individual aerosol species: black carbon (BC) from fossil fuel and biomass burning, sulfate, organic aerosols (OAs), dust, and sea-salt. For a subset of models that represent nitrate and secondary organic aerosols (SOAs), we document the role of these aerosols at high latitudes. The seasonal dependence of natural and anthropogenic aerosols differs with natural aerosols peaking in winter (seasalt) and spring (dust), whereas AOD from anthropogenic aerosols peaks in late spring and summer. The models produce a median annual mean AOD of 0.07 in the Arctic (defined here as north of 60 degrees N). The models also predict a noteworthy aerosol transport to the Antarctic (south of 70 degrees S) with a resulting AOD varying between 0.01 and 0.02. The models have estimated the shortwave anthropogenic radiative forcing contributions to the direct aerosol effect (DAE) associated with BC and OA from fossil fuel and biofuel (FF), sulfate, SOAs, nitrate, and biomass burning from BC and OA emissions combined. The Arctic modelled annual mean DAE is slightly negative (-0.12 W m(exp. -2), dominated by a positive BC FF DAE in spring and a negative sulfate DAE in summer. The Antarctic DAE is governed by BC FF. We perform sensitivity experiments with one of the AeroCom models (GISS modelE) to investigate how regional emissions of BC and sulfate and the lifetime of BC influence the Arctic and Antarctic AOD. A doubling of emissions in eastern Asia results in a 33 percent increase in Arctic AOD of BC. A doubling of the BC lifetime results in a 39 percent increase in Arctic AOD of BC. However, these radical changes still fall within the AeroCom model range.
    Keywords: Meteorology and Climatology; Earth Resources and Remote Sensing
    Type: GSFC-E-DAA-TN48871 , Atmospheric Chemistry and Physics (ISSN 1680-7316) (e-ISSN 1680-7324); 17; 19; 12197-12218
    Format: text
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  • 4
    Publication Date: 2021-10-07
    Description: Volcanic eruptions are an important climate driver. The impact of Pinatubo-sized eruptions has been observed and is well constrained. The magnitude and duration of volcanic winter effects after supereruptions such as Toba remain disputed due to disagreement between the strong cooling predicted by models and much milder climate perturbations according to the paleodata. Here we present a reevaluated climate impact of a Toba-sized supereruption based on up-to-date GISS ModelE simulations. In this study, we account for all known primary mechanisms that govern the evolution of the volcanic plume and their nonlinear interactions. The SO 2 radiative effects are evaluated for the first time in coupled climate simulations with the interactive atmospheric chemistry module. We found that SO 2 effects on photochemistry, dynamics, and radiative forcing are especially prominent. Due to strong absorption in ultraviolet, SO 2 feedback on photochemistry partially offsets the limiting effect associated with aerosol microphysical processes. SO 2 greenhouse warming soothes the radiative cooling exerted by sulfate aerosols. SO 2 absorption in the shortwave and longwave causes radiative heating and lofting of the volcanic plume, and boosts the efficiency of SO 2 impact on photochemistry. Our analysis shows that SO 2 lifetime and magnitude of effects scale up and increase with the amount of emitted material. For a Pinatubo-sized eruption, SO 2 feedbacks on chemistry and dynamics are relevant only during the initial stage of the volcanic plume evolution, while local SO 2 concentrations are high. For a Toba-sized eruption, SO 2 effects are as important as sulfate aerosols and produce a less extreme volcanic winter.
    Keywords: 551.5 ; supereruption ; Toba ; volcanic winter ; sulfate aerosols ; climate impact ; sulfur dioxide
    Language: English
    Type: map
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