scholarly journals Impact of the Ambae, Raikoke and Ulawun eruptions in 2018-2019 on the global stratospheric aerosol layer and climate

Author(s):  
Corinna Kloss ◽  
Pasquale Sellitto ◽  
Bernard Legras ◽  
Jean-Paul Vernier ◽  
Fabrice Jégou ◽  
...  

<p>Using a combination of satellite, ground-based and in-situ observations, and radiative transfer modelling, we quantify the impact of the most recent moderate volcanic eruptions (Ambae, Vanuatu in July 2018; Raikoke, Russia and Ulawun, New Guinea in June 2019) on the global stratospheric aerosol layer and climate.</p><p>For the Ambae volcano (15°S and 167°E), we use the Stratospheric Aerosol and Gas Experiment III (SAGE III), the Ozone Mapping Profiler Suite (OMPS), the Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) and Himawari geostationary satellite observations of the aerosol plume evolution following the Ambae eruption of July 2018. It is shown that the aerosol plume of the main eruption at Ambae in July 2018 was distributed throughout the global stratosphere within the global large-scale circulation (Brewer-Dobson circulation, BDC), to both hemispheres. Ground-based LiDAR observations in Gadanki, India, as well as in-situ Printed Optical Particle Spectrometer (POPS) measurements acquired during the BATAL campaign confirm a widespread perturbation of the stratospheric aerosol layer due to this eruption. Using the UVSPEC radiative transfer model, we also estimate the radiative forcing of this global stratospheric aerosol perturbation. The climate impact is shown to be comparable to that of the well-known and studied recent moderate stratospheric eruptions from Kasatochi (USA, 2008), Sarychev (Russia, 2009) and Nabro (Eritrea, 2011). Top of the atmosphere radiative forcing values between -0.45 and -0.60 W/m<sup>2</sup>, for the Ambae eruption of July 2018, are found.</p><p>In a similar manner the dispersion of the aerosol plume of the Raikoke (48°N and 153°E) and Ulawun (5°S and 151°E) eruptions of June 2019 is analyzed. As both of those eruptions had a stratospheric impact and happened almost simultaneously, it is challenging to completely distinguish both events. Even though the eruptions occurred very recently, first results show that the aerosol plume of the Raikoke eruption resulted in an increase in aerosol extinction values, double as high as compared to that of the Ambae eruption. However, as the eruption occurred on higher latitudes, the main bulk of Raikoke aerosols was transported towards the northern higher latitude’s in the stratosphere within the BDC, as revealed by OMPS, SAGE III and a new detection algorithm for SO<sub>2</sub> and sulfate aerosol using IASI (Infrared Atmospheric Sounder Interferometer). Even though the Raikoke eruption had a larger impact on the stratospheric aerosol layer, both events (the eruptions at Raikoke and Ambae) have to be considered in stratospheric aerosol budget and climate studies.</p>

2021 ◽  
Author(s):  
Jie Gao ◽  
Jonathon Wright

<p>The Asian Tropopause Aerosol Layer (ATAL) has emerged over recent decades to play an increasingly prominent role in the upper troposphere and lower stratosphere above the Asian monsoon region. Although the effects of the ATAL on the surface and top-of-atmosphere radiation budget have been examined by several studies, the processes and effects by which the ATAL alters radiative transfer within the tropopause layer have been much less discussed. We have used a conditional composite approach to investigate aerosol mixing ratios and their impacts on radiative heating rates in the Asian monsoon tropopause layer in MERRA-2. We have then subsampled in time based on known volcanic eruptions and the evolution of emission and data assimilation inputs to the MERRA-2 aerosol analysis to isolate the ATAL contribution and compare it to radiative heating signatures in the monsoon anticyclone region after volcanic eruptions. The results indicate that the ATAL impact on radiative heating rates in this region is on the order of 0.1 K/day, similar to that associated with ozone variability in MERRA-2 but weaker than cloud radiative effects at these altitudes. We have validated these results and tested their sensitivity to variations in the vertical structure and composition of ATAL aerosols using offline radiative transfer simulations. The idealized simulations produce similar but slightly stronger responses of radiative heating rates to the ATAL and are in good agreement with previous estimates of the top-of-atmosphere radiative forcing. Although the ATAL perturbations inferred from MERRA-2 are only about 10% of mean heating rates at these levels, their spatial distribution suggests potential implications for both isentropic and diabatic transport within the monsoon anticyclone, which should be examined in future work. Our results are limited by uncertainties in the composition and spatiotemporal variability of the ATAL, and reflect only the conditions in this layer as represented by MERRA-2. Targeted observations and model simulations are needed to adequately constrain the uncertainties, particularly with respect to the relative proportions and contributions of nitrate aerosols, which are not included in the MERRA-2 aerosol analysis.</p>


2021 ◽  
Author(s):  
Filippo Calì Quaglia ◽  
Daniela Meloni ◽  
Alcide Giorgio di Sarra ◽  
Tatiana Di Iorio ◽  
Virginia Ciardini ◽  
...  

<p>Extended and intense wildfires occurred in Northern Canada and, unexpectedly, on the Greenlandic West coast during summer 2017. The thick smoke plume emitted into the atmosphere was transported to the high Arctic, producing one of the largest impacts ever observed in the region. Evidence of Canadian and Greenlandic wildfires was recorded at the Thule High Arctic Atmospheric Observatory (THAAO, 76.5°N, 68.8°W, www.thuleatmos-it.it) by a suite of instruments managed by ENEA, INGV, Univ. of Florence, and NCAR. Ground-based observations of the radiation budget have allowed quantification of the surface radiative forcing at THAAO. </p><p>Excess biomass burning chemical tracers such as CO, HCN, H2CO, C2H6, and NH3 were  measured in the air column above Thule starting from August 19 until August 23. The aerosol optical depth (AOD) reached a peak value of about 0.9 on August 21, while an enhancement of wildfire compounds was  detected in PM10. The measured shortwave radiative forcing was -36.7 W/m2 at 78° solar zenith angle (SZA) for AOD=0.626.</p><p>MODTRAN6.0 radiative transfer model (Berk et al., 2014) was used to estimate the aerosol radiative effect and the heating rate profiles at 78° SZA. Measured temperature profiles, integrated water vapour, surface albedo, spectral AOD and aerosol extinction profiles from CALIOP onboard CALIPSO were used as model input. The peak  aerosol heating rate (+0.5 K/day) was  reached within the aerosol layer between 8 and 12 km, while the maximum radiative effect (-45.4 W/m2) is found at 3 km, below the largest aerosol layer.</p><p>The regional impact of the event that occurred on August 21 was investigated using a combination of atmospheric radiative transfer modelling with measurements of AOD and ground surface albedo from MODIS. The aerosol properties used in the radiative transfer model were constrained by in situ measurements from THAAO. Albedo data over the ocean have been obtained from Jin et al. (2004). Backward trajectories produced through HYSPLIT simulations (Stein et al., 2015) were also employed to trace biomass burning plumes.</p><p>The radiative forcing efficiency (RFE) over land and ocean was derived, finding values spanning from -3 W/m2 to -132 W/m2, depending on surface albedo and solar zenith angle. The fire plume covered a vast portion of the Arctic, with large values of the daily shortwave RF (< -50 W/m2) lasting for a few days. This large amount of aerosol is expected to influence cloud properties in the Arctic, producing significant indirect radiative effects.</p>


2019 ◽  
Vol 12 (11) ◽  
pp. 6173-6191 ◽  
Author(s):  
Jayanta Kar ◽  
Kam-Pui Lee ◽  
Mark A. Vaughan ◽  
Jason L. Tackett ◽  
Charles R. Trepte ◽  
...  

Abstract. In August 2018, the Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) project released a new level 3 stratospheric aerosol profile data product derived from nearly 12 years of measurements acquired by the spaceborne Cloud–Aerosol Lidar with Orthogonal Polarization (CALIOP). This monthly averaged, gridded level 3 product is based on version 4 of the CALIOP level 1B and level 2 data products, which feature significantly improved calibration that now makes it possible to reliably retrieve profiles of stratospheric aerosol extinction and backscatter coefficients at 532 nm. This paper describes the science algorithm and data handling techniques that were developed to generate the CALIPSO version 1.00 level 3 stratospheric aerosol profile product. Further, we show that the extinction profiles (retrieved using a constant lidar ratio of 50 sr) capture the major stratospheric perturbations in both hemispheres over the last decade resulting from volcanic eruptions, extreme smoke events, and signatures of stratospheric dynamics. Initial assessment of the product by intercomparison with the stratospheric aerosol retrievals from the Stratospheric Aerosol and Gas Experiment III (SAGE III) on the International Space Station (ISS) indicates good agreement in the tropical stratospheric aerosol layer (30∘ N–30∘ S), where the average difference between zonal mean extinction profiles is typically less than 25 % between 20 and 30 km (CALIPSO biased high). However, differences can exceed 100 % in the very low aerosol loading regimes found above 25 km at higher latitudes. Similarly, there are large differences (≥100 %) within 2 to 3 km above the tropopause that might be due to cloud contamination issues.


2017 ◽  
Vol 17 (18) ◽  
pp. 10937-10953 ◽  
Author(s):  
Bengt G. Martinsson ◽  
Johan Friberg ◽  
Oscar S. Sandvik ◽  
Markus Hermann ◽  
Peter F. J. van Velthoven ◽  
...  

Abstract. This study is based on fine-mode aerosol samples collected in the upper troposphere (UT) and the lowermost stratosphere (LMS) of the Northern Hemisphere extratropics during monthly intercontinental flights at 8.8–12 km altitude of the IAGOS-CARIBIC platform in the time period 1999–2014. The samples were analyzed for a large number of chemical elements using the accelerator-based methods PIXE (particle-induced X-ray emission) and PESA (particle elastic scattering analysis). Here the particulate sulfur concentrations, obtained by PIXE analysis, are investigated. In addition, the satellite-borne lidar aboard CALIPSO is used to study the stratospheric aerosol load. A steep gradient in particulate sulfur concentration extends several kilometers into the LMS, as a result of increasing dilution towards the tropopause of stratospheric, particulate sulfur-rich air. The stratospheric air is diluted with tropospheric air, forming the extratropical transition layer (ExTL). Observed concentrations are related to the distance to the dynamical tropopause. A linear regression methodology handled seasonal variation and impact from volcanism. This was used to convert each data point into stand-alone estimates of a concentration profile and column concentration of particulate sulfur in a 3 km altitude band above the tropopause. We find distinct responses to volcanic eruptions, and that this layer in the LMS has a significant contribution to the stratospheric aerosol optical depth and thus to its radiative forcing. Further, the origin of UT particulate sulfur shows strong seasonal variation. We find that tropospheric sources dominate during the fall as a result of downward transport of the Asian tropopause aerosol layer (ATAL) formed in the Asian monsoon, whereas transport down from the Junge layer is the main source of UT particulate sulfur in the first half of the year. In this latter part of the year, the stratosphere is the clearly dominating source of particulate sulfur in the UT during times of volcanic influence and under background conditions.


2018 ◽  
Vol 11 (7) ◽  
pp. 2581-2608 ◽  
Author(s):  
Claudia Timmreck ◽  
Graham W. Mann ◽  
Valentina Aquila ◽  
Rene Hommel ◽  
Lindsay A. Lee ◽  
...  

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.


2021 ◽  
Vol 21 (8) ◽  
pp. 6565-6591
Author(s):  
Clarissa Alicia Kroll ◽  
Sally Dacie ◽  
Alon Azoulay ◽  
Hauke Schmidt ◽  
Claudia Timmreck

Abstract. Increasing the temperature of the tropical cold-point region through heating by volcanic aerosols results in increases in the entry value of stratospheric water vapor (SWV) and subsequent changes in the atmospheric energy budget. We analyze tropical volcanic eruptions of different strengths with sulfur (S) injections ranging from 2.5 Tg S up to 40 Tg S using EVAens, the 100-member ensemble of the Max Planck Institute – Earth System Model in its low-resolution configuration (MPI-ESM-LR) with artificial volcanic forcing generated by the Easy Volcanic Aerosol (EVA) tool. Significant increases in SWV are found for the mean over all ensemble members from 2.5 Tg S onward ranging between [5, 160] %. However, for single ensemble members, the standard deviation between the control run members (0 Tg S) is larger than SWV increase of single ensemble members for eruption strengths up to 20 Tg S. A historical simulation using observation-based forcing files of the Mt. Pinatubo eruption, which was estimated to have emitted (7.5±2.5) Tg S, returns SWV increases slightly higher than the 10 Tg S EVAens simulations due to differences in the aerosol profile shape. An additional amplification of the tape recorder signal is also apparent, which is not present in the 10 Tg S run. These differences underline that it is not only the eruption volume but also the aerosol layer shape and location with respect to the cold point that have to be considered for post-eruption SWV increases. The additional tropical clear-sky SWV forcing for the different eruption strengths amounts to [0.02, 0.65] W m−2, ranging between [2.5, 4] % of the aerosol radiative forcing in the 10 Tg S scenario. The monthly cold-point temperature increases leading to the SWV increase are not linear with respect to aerosol optical depth (AOD) nor is the corresponding SWV forcing, among others, due to hysteresis effects, seasonal dependencies, aerosol profile heights and feedbacks. However, knowledge of the cold-point temperature increase allows for an estimation of SWV increases of 12 % per Kelvin increase in mean cold-point temperature. For yearly averages, power functions are fitted to the cold-point warming and SWV forcing with increasing AOD.


2017 ◽  
Author(s):  
Nelson Bègue ◽  
Damien Vignelles ◽  
Gwenaël Berthet ◽  
Thierry Portafaix ◽  
Guillaume Payen ◽  
...  

Abstract. After 43 years of inactivity, the Calbuco volcano which is located in the southern part of Chile erupted on 22 April 2015. The space-time evolutions (distribution and transport) of its aerosol plume are investigated by combining satellite (CALIOP, IASI, OMPS), in situ aerosol counting (LOAC OPC) and lidar observations, and the MIMOSA advection model. The Calbuco aerosol plume reached the Indian Ocean 1 week after the eruption. Over the Reunion Island site (21° S; 55.5° E), the aerosol signal was unambiguously enhanced in comparison with "background" conditions with a volcanic aerosol layer extending from 18 km to 21 km during the May–July period. All the data reveal an increase by a factor of ~ 2 in the SAOD (Stratospheric Aerosol Optical Depth) with respect to values observed before the eruption. The aerosol e-folding time is approximately 90 days. Microphysical measurements obtained before, during and after the eruption reflecting the impact of the Calbuco eruption on the lower stratospheric aerosol content have been analyzed over Reunion site. During the passage of the plume, the volcanic aerosol was characterized by an effective radius of 0.16 ± 0.02 µm with an unimodal lognormal size distribution and the aerosol number concentration appears 20 times higher than before and one year after the eruption. A tendency toward "background" conditions has been observed about one year after the eruption, by April 2016. The volcanic aerosol plume is advected eastward in the Southern Hemisphere and its latitudinal extent is clearly bounded by the subtropical barrier and the polar vortex. The transient behavior of the aerosol layers observed above Reunion Island between May and July 2015 reflects an inhomogeneous geographical distribution of the plume which is controlled by the latitudinal motion of these dynamical barriers.


2020 ◽  
Vol 20 (11) ◽  
pp. 6821-6839 ◽  
Author(s):  
Fernando Chouza ◽  
Thierry Leblanc ◽  
John Barnes ◽  
Mark Brewer ◽  
Patrick Wang ◽  
...  

Abstract. As part of the Network for the Detection of Atmospheric Composition Change (NDACC), ground-based measurements obtained from the Jet Propulsion Laboratory (JPL) stratospheric ozone lidar and the NOAA stratospheric aerosol lidar at Mauna Loa, Hawaii, over the past 2 decades were used to investigate the impact of volcanic eruptions and pyrocumulonimbus (PyroCb) smoke plumes on the stratospheric aerosol load above Hawaii since 1999. Measurements at 355 and 532 nm conducted by these two lidars revealed a color ratio of 0.5 for background aerosols and small volcanic plumes and 0.8 for a PyroCb plume recorded on September 2017. Measurements of the Nabro plume by the JPL lidar in 2011–2012 showed a lidar ratio of (64±12.7) sr at 355 nm around the center of the plume. The new Global Space-based Stratospheric Aerosol Climatology (GloSSAC), Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP) Level 3 and Stratospheric Aerosol and Gas Experiment III on the International Space Station (SAGE III-ISS) stratospheric aerosol datasets were compared to the ground-based lidar datasets. The intercomparison revealed a generally good agreement, with vertical profiles of extinction coefficient within 50 % discrepancy between 17 and 23 km above sea level (a.s.l.) and 25 % above 23 km a.s.l. The stratospheric aerosol depth derived from all of these datasets shows good agreement, with the largest discrepancy (20 %) being observed between the new CALIOP Level 3 and the other datasets. All datasets consistently reveal a relatively quiescent period between 1999 and 2006, followed by an active period of multiple eruptions (e.g., Nabro) until early 2012. Another quiescent period, with slightly higher aerosol background, lasted until mid-2017, when a combination of extensive wildfires and multiple volcanic eruptions caused a significant increase in stratospheric aerosol loading. This loading maximized at the very end of the time period considered (fall 2019) as a result of the Raikoke eruption, the plume of which ascended to 26 km altitude in less than 3 months.


2017 ◽  
Author(s):  
Thibaut Lurton ◽  
Fabrice Jégou ◽  
Gwenaël Berthet ◽  
Jean-Baptiste Renard ◽  
Lieven Clarisse ◽  
...  

Abstract. Volcanic eruptions impact climate through the injection of sulfur dioxide (SO2), which is oxidized to form sulfuric acid aerosol particles that can enhance the stratospheric aerosol optical depth (SAOD). Besides large-magnitude eruptions, moderate-magnitude eruptions such as Kasatochi in 2008 and Sarychev Peak in 2009 can have a significant impact on stratospheric aerosol and hence climate. However, uncertainties remain in quantifying the atmospheric and climatic impacts of the 2009 Sarychev Peak eruption due to limitations in previous model representations of volcanic aerosol microphysics and particle size, whilst biases have been identified in satellite estimates of post-eruption SAOD. In addition, the 2009 Sarychev Peak eruption co-injected hydrogen chloride (HCl) alongside SO2, whose potential stratospheric chemistry impacts have not been investigated to date. We present a study of the stratospheric SO2-particle-HCl processing and impacts following Sarychev Peak eruption, using the CESM1(WACCM)-CARMA sectional aerosol microphysics model (with no a priori assumption on particle size). The Sarychev Peak 2009 eruption injected 0.9 Tg of SO2 into the upper troposphere and lower stratosphere (UTLS), enhancing the aerosol load in the Northern hemisphere. The post-eruption evolution of the volcanic SO2 in space and time are well reproduced by the model when compared to IASI (Infrared Atmospheric Sounding Interferometer) satellite data. Co-injection of 27 Gg HCl causes a lengthening of the SO2 lifetime and a slight delay in the formation of aerosols, and acts to enhance the destruction of stratospheric ozone and mono-nitrogen oxides (NOx) compared to the simulation with volcanic SO2 only. We therefore highlight the need to account for volcanic halogen chemistry when simulating the impact of eruptions such as Sarychev on stratospheric chemistry. The model-simulated evolution of effective radius (reff), reflects new particle formation followed by particle growth that enhances reff to reach up to 0.2 µm on zonal average. Comparisons of the model-simulated particle number and size-distributions to balloon-borne in-situ stratospheric observations over Kiruna, Sweden, in August and September 2009, and over Laramie, U.S.A., in June and November 2009 show good agreement and quantitatively confirms the post-eruption particle enhancement. We show that the model-simulated SAOD is consistent with that derived from OSIRIS (Optical Spectrograph and InfraRed Imager System) when both the saturation bias of OSIRIS and the fact that extinction profiles may terminate well above the tropopause are taken into account. Previous modelling studies (involving assumptions on particle size) that reported agreement to (biased) post-eruption estimates of SAOD derived from OSIRIS likely underestimated the climate impact of the 2009 Sarychev Peak eruption.


2019 ◽  
Author(s):  
Jayanta Kar ◽  
Kam-Pui Lee ◽  
Mark A. Vaughan ◽  
Jason L. Tackett ◽  
Charles R. Trepte ◽  
...  

Abstract. In August 2018, the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) project released a new level 3 stratospheric aerosol profile data product derived from nearly 12 years of measurements acquired by the space-borne Cloud-Aerosol Lidar with Orthogonal Polarization (CALIOP). This monthly averaged, gridded level 3 product is based on version 4.2 of the CALIOP level 1 and level 2 data products, which feature significantly improved calibration that now makes it possible to reliably retrieve profiles of stratospheric aerosol extinction and backscatter coefficients. This paper describes the science algorithm and data handling techniques that were developed to generate the CALIPSO version 1.00 level 3 stratospheric aerosol profile product. Further, we show that the retrieved extinction profiles capture the major stratospheric perturbations over the last decade resulting from volcanic eruptions, extreme smoke events, and signatures of stratospheric dynamics. Initial assessment of the product by inter-comparison with the stratospheric aerosol retrievals from the Stratospheric Aerosol and Gas Experiment III (SAGE III) on the International Space Station (ISS) indicates good agreement in the tropical stratospheric aerosol layer (30° N–30° S), where the average difference between zonal mean extinction profiles is typically less than 25 % between 20 km and 30 km. However, differences can exceed 100 % in the very low aerosol loading regimes found above 25 km at higher latitudes.


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