Articles | Volume 26, issue 12
https://doi.org/10.5194/acp-26-8999-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-26-8999-2026
© Author(s) 2026. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
A global view of the stratospheric background, volcanic and wildfire aerosol in the CALIOP era (2006–2023)
Bengt G. Martinsson
CORRESPONDING AUTHOR
Department of Physics, Lund University, Lund, Sweden
Johan Friberg
Department of Physics, Lund University, Lund, Sweden
Moa K. Sporre
Department of Physics, Lund University, Lund, Sweden
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Highly variable stratospheric aerosol bears great importance for Earth's climate. The 1-year average aerosol load from the 2022 volcanic eruption in Hunga Tonga is the highest since the 1991 Mt. Pinatubo eruption. The usual volcanic aerosol precursor gas (SO2) mass was not sufficient to explain the aerosol load. Intense volcanism–sea interaction amplified the eruption, and sea salt emission forms a plausible explanation for the high aerosol loading.
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Large amounts of wildfire smoke reached the stratosphere in 2017. The literature on stratospheric aerosol is mainly based on horizontally viewing sensors that saturate in dense smoke. Using also a vertically viewing sensor with orders of magnitude shorter path in the smoke, we show that the horizontally viewing sensors miss a dramatic exponential decline of the aerosol load with a half-life of 10 d, where 80 %–90 % of smoke is lost. We attribute the decline to photolytic loss of organic aerosol.
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A method to form SO2 profiles in the stratosphere with high vertical resolution following volcanic eruptions is introduced. The method combines space-based high-resolution vertical aerosol profiles and SO2 measurements the first 2 weeks after an eruption with air mass trajectory analyses. The SO2 is located at higher altitude than in most previous studies. The detailed resolution of the SO2 profile is unprecedented compared to other methods.
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Highly variable stratospheric aerosol bears great importance for Earth's climate. The 1-year average aerosol load from the 2022 volcanic eruption in Hunga Tonga is the highest since the 1991 Mt. Pinatubo eruption. The usual volcanic aerosol precursor gas (SO2) mass was not sufficient to explain the aerosol load. Intense volcanism–sea interaction amplified the eruption, and sea salt emission forms a plausible explanation for the high aerosol loading.
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We investigate the importance of using high-vertical-resolution (HR) SO2 data when simulating volcanic eruptions' impact on the stratospheric aerosol load and climate, using WACCM, and compare simulations with aerosol observations from CALIOP. Simulations with HR SO2 data match the observations well, whereas simulations with the model's default low-resolution (LR) data underestimate the aerosol load by ~ 50 %. The resulting climate cooling is twice as high for the HR than the LR SO2 data.
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We study the short- and long-term stratospheric impact of smoke from the massive Australian wildfires in Dec 2019–Jan 2020 using four satellite sensors. Smoke entered the stratosphere rapidly via transport by firestorms, as well as weeks after the fires. The smoke particle properties evolved over time together with rapidly decreasing stratospheric aerosol load, suggesting photolytic loss of organics in the smoke particles. The depletion rate was estimated to a half-life (e folding) of 10 (14) d.
Bengt G. Martinsson, Johan Friberg, Oscar S. Sandvik, and Moa K. Sporre
Atmos. Chem. Phys., 22, 3967–3984, https://doi.org/10.5194/acp-22-3967-2022, https://doi.org/10.5194/acp-22-3967-2022, 2022
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Large amounts of wildfire smoke reached the stratosphere in 2017. The literature on stratospheric aerosol is mainly based on horizontally viewing sensors that saturate in dense smoke. Using also a vertically viewing sensor with orders of magnitude shorter path in the smoke, we show that the horizontally viewing sensors miss a dramatic exponential decline of the aerosol load with a half-life of 10 d, where 80 %–90 % of smoke is lost. We attribute the decline to photolytic loss of organic aerosol.
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Oscar S. Sandvik, Johan Friberg, Moa K. Sporre, and Bengt G. Martinsson
Atmos. Meas. Tech., 14, 7153–7165, https://doi.org/10.5194/amt-14-7153-2021, https://doi.org/10.5194/amt-14-7153-2021, 2021
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A method to form SO2 profiles in the stratosphere with high vertical resolution following volcanic eruptions is introduced. The method combines space-based high-resolution vertical aerosol profiles and SO2 measurements the first 2 weeks after an eruption with air mass trajectory analyses. The SO2 is located at higher altitude than in most previous studies. The detailed resolution of the SO2 profile is unprecedented compared to other methods.
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Short summary
The highly variable stratospheric aerosol with great importance for the Earth’s climate was investigated with the satellite-based lidar CALIOP (Cloud-Aerosol LIdar with Orthogonal Polarization) during its entire active period 2006–2023. The background aerosol was identified, showing excellent agreement with solar occultation from the volcanically quiescent period (1998–2000), and indicate strong influence from carbonyl sulfide. 15 volcanic eruptions and 5 wildfires caused variability, from background radiative forcing of -0.14 to -0.4 W/m2.
The highly variable stratospheric aerosol with great importance for the Earth’s climate was...
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