Aerosols as dynamical tracers in the lower stratosphere: Ozone versus aerosol correlation after the Mount Pinatubo eruption

1995 ◽  
Vol 100 (D6) ◽  
pp. 11147 ◽  
Author(s):  
S. Borrmann ◽  
J. E. Dye ◽  
D. Baumgardner ◽  
M. H. Proffitt ◽  
J. J. Margitan ◽  
...  
2015 ◽  
Vol 15 (23) ◽  
pp. 13507-13518 ◽  
Author(s):  
M. Fujiwara ◽  
T. Hibino ◽  
S. K. Mehta ◽  
L. Gray ◽  
D. Mitchell ◽  
...  

Abstract. The global temperature responses to the eruptions of Mount Agung in 1963, El Chichón in 1982, and Mount Pinatubo in 1991 are investigated using nine currently available reanalysis data sets (JRA-55, MERRA, ERA-Interim, NCEP-CFSR, JRA-25, ERA-40, NCEP-1, NCEP-2, and 20CR). Multiple linear regression is applied to the zonal and monthly mean time series of temperature for two periods, 1979–2009 (for eight reanalysis data sets) and 1958–2001 (for four reanalysis data sets), by considering explanatory factors of seasonal harmonics, linear trends, Quasi-Biennial Oscillation, solar cycle, and El Niño Southern Oscillation. The residuals are used to define the volcanic signals for the three eruptions separately, and common and different responses among the older and newer reanalysis data sets are highlighted for each eruption. In response to the Mount Pinatubo eruption, most reanalysis data sets show strong warming signals (up to 2–3 K for 1-year average) in the tropical lower stratosphere and weak cooling signals (down to −1 K) in the subtropical upper troposphere. For the El Chichón eruption, warming signals in the tropical lower stratosphere are somewhat smaller than those for the Mount Pinatubo eruption. The response to the Mount Agung eruption is asymmetric about the equator with strong warming in the Southern Hemisphere midlatitude upper troposphere to lower stratosphere. Comparison of the results from several different reanalysis data sets confirms the atmospheric temperature response to these major eruptions qualitatively, but also shows quantitative differences even among the most recent reanalysis data sets. The consistencies and differences among different reanalysis data sets provide a measure of the confidence and uncertainty in our current understanding of the volcanic response. The results of this intercomparison study may be useful for validation of climate model responses to volcanic forcing and for assessing proposed geoengineering by stratospheric aerosol injection, as well as to link studies using only a single reanalysis data set to other studies using a different reanalysis data set.


2015 ◽  
Vol 15 (9) ◽  
pp. 13315-13346 ◽  
Author(s):  
M. Fujiwara ◽  
T. Hibino ◽  
S. K. Mehta ◽  
L. Gray ◽  
D. Mitchell ◽  
...  

Abstract. Global temperature response to the eruptions of Mount Agung in 1963, El Chichón in 1982 and Mount Pinatubo in 1991 is investigated using nine reanalysis datasets (JRA-55, MERRA, ERA-Interim, NCEP-CFSR, JRA-25, ERA-40, NCEP-1, NCEP-2, and 20CR). Multiple linear regression is applied to the zonal and monthly mean time series of temperature for two periods, 1979–2009 (for eight reanalysis datasets) and 1958–2001 (for four reanalysis datasets), by considering explanatory factors of seasonal harmonics, linear trends, Quasi-Biennial Oscillation, solar cycle, and El Niño Southern Oscillation. The residuals are used to define the volcanic signals for the three eruptions separately. In response to the Mount Pinatubo eruption, most reanalysis datasets show strong warming signals (up to 2–3 K for one-year average) in the tropical lower stratosphere and weak cooling signals (down to −1 K) in the subtropical upper troposphere. For the El Chichón eruption, warming signals in the tropical lower stratosphere are somewhat smaller than those for the Mount Pinatubo eruption. The response to the Mount Agung eruption is asymmetric about the equator with strong warming in the Southern Hemisphere midlatitude upper troposphere to lower stratosphere. The response to three other smaller-scale eruptions in the 1960s and 1970s is also investigated. Comparison of the results from several different reanalysis datasets confirms the atmospheric temperature response to these major eruptions qualitatively, but also shows quantitative differences even among the most recent reanalysis datasets.


2017 ◽  
Author(s):  
Laura Revell ◽  
Andrea Stenke ◽  
Beiping Luo ◽  
Stefanie Kremser ◽  
Eugene Rozanov ◽  
...  

Abstract. To simulate the impacts of volcanic eruptions on the stratosphere, chemistry-climate models that do not include an online aerosol module require temporally and spatially resolved aerosol size parameters for heterogeneous chemistry and aerosol radiative properties as a function of wavelength. For phase 1 of the Chemistry-Climate Model Initiative (CCMI-1) and, later, for phase 6 of the Coupled Model Intercomparison Project (CMIP6) two such stratospheric aerosol data sets were compiled, whose functional capability and representativeness are compared here. For CCMI-1, the SAGE-4λ data set was compiled, which hinges on the measurements at four wavelengths of the SAGE (Stratospheric Aerosol and Gas Experiment) II satellite instrument and uses ground-based Lidar measurements for gap-filling immediately after the Mt. Pinatubo eruption, when the stratosphere was optically opaque for SAGE II. For CMIP6, the new SAGE-3λ data set was compiled, which excludes the least reliable SAGE II wavelength and uses CLAES (Cryogenic Limb Array Etalon Spectrometer) measurements on UARS, the Upper Atmosphere Research Satellite, for gap-filling following the Mt. Pinatubo eruption instead of ground-based Lidars. Here, we performed SOCOLv3 (Solar Climate Ozone Links version 3) chemistry-climate model simulations of the recent past (1986–2005) to investigate the impact of the Mt. Pinatubo eruption in 1991 on stratospheric temperature and ozone and how this response differs depending on which aerosol data set is applied. The use of SAGE-4λ results in heating and ozone loss being overestimated in the lower stratosphere compared to observations in the post-eruption period by approximately 3 K and 0.2 ppmv, respectively. However, less heating occurs in the model simulations based on SAGE-3λ, because the improved gap-filling procedures after the eruption lead to less aerosol loading in the tropical lower stratosphere. As a result, simulated temperature anomalies in the model simulations based on SAGE-3λ for CMIP6 are in excellent agreement with MERRA and ERA-Interim reanalyses in the post-eruption period. Less heating in the simulations with SAGE-3λ means that the rate of tropical upwelling does not strengthen as much as it does in the simulations with SAGE-4λ, which limits dynamical uplift of ozone and therefore provides more time for ozone to accumulate in tropical mid-stratospheric air. Ozone loss following the Mt. Pinatubo eruption is overestimated by 0.1 ppmv in the model simulations based on SAGE-3λ, which is a better agreement with observations than in the simulations based on SAGE-4λ. Overall, the CMIP6 stratospheric aerosol data set, SAGE-3λ, allows SOCOLv3 to more accurately simulate the post-Pinatubo eruption period.


1996 ◽  
Author(s):  
David C. Woods ◽  
David M. Winker ◽  
Otto Youngbluth, Jr. ◽  
Mary T. Osborn ◽  
Robert J. DeCoursey

2015 ◽  
Vol 15 (20) ◽  
pp. 11501-11512 ◽  
Author(s):  
J.-X. Sheng ◽  
D. K. Weisenstein ◽  
B.-P. Luo ◽  
E. Rozanov ◽  
F. Arfeuille ◽  
...  

Abstract. We have performed more than 300 atmospheric simulations of the 1991 Pinatubo eruption using the AER 2-D sulfate aerosol model to optimize the initial sulfur mass injection as a function of altitude, which in previous modeling studies has often been chosen in an ad hoc manner (e.g., by applying a rectangular-shaped emission profile). Our simulations are generated by varying a four-parameter vertical mass distribution, which is determined by a total injection mass and a skew-normal distribution function. Our results suggest that (a) the initial mass loading of the Pinatubo eruption is approximately 14 Mt of SO2; (b) the injection vertical distribution is strongly skewed towards the lower stratosphere, leading to a peak mass sulfur injection at 18–21 km; (c) the injection magnitude and height affect early southward transport of the volcanic clouds as observed by SAGE II.


2014 ◽  
Vol 14 (2) ◽  
pp. 2799-2855 ◽  
Author(s):  
S. S. Dhomse ◽  
K. M. Emmerson ◽  
G. W. Mann ◽  
N. Bellouin ◽  
K. S. Carslaw ◽  
...  

Abstract. We have enhanced the capability of a microphysical aerosol-chemistry module to simulate the atmospheric aerosol and precursor gases for both tropospheric and stratospheric conditions. Using the Mount Pinatubo eruption (June 1991) as a test case, we evaluate simulated aerosol properties in a composition-climate model against a range of satellite and in-situ observations. Simulations are performed assuming an injection of 20 Tg SO2 at 19–27 km in tropical latitudes, without any radiative feedback from the simulated aerosol. In both quiescent and volcanically perturbed conditions, simulated aerosol properties in the lower stratosphere show reasonable agreement with the observations. The model captures the observed timing of the maximum aerosol optical depth (AOD) and its decay timescale in both tropics and Northern Hemisphere (NH) mid-latitudes. There is also good qualitative agreement with the observations in terms of spatial and temporal variation of the aerosol effective radius (Reff), which peaks 6–8 months after the eruption. However, the model shows significant biases against some observational data sets. Simulated AOD and Surface Area Density (SAD) in the tropics are substantially higher than the gap-filled satellite data products during the first 6 months after the eruption. The model shows consistently weaker enhancement in Reff compared to satellite and in-situ measurements. Simulated aerosol particle size distribution is also compared to NH mid-latitude in-situ balloon sounding measurements of size-resolved number concentrations. Before the eruption, the model captures the observed profiles of lower stratospheric particle number concentrations with radii larger than 5, 150 and 250 nm (N5, N150 and N250) very well. However, in the first 6 months after the eruption, the model shows high bias in N5 concentrations in the lower stratosphere, suggesting too strong nucleation. Following particle growth via condensation and coagulation, this bias in the finest particles propagates into a factor 2 high bias in N150. Our comparison suggests that new particle formation in the initial phase of large eruptions, and subsequent particle growth to optically-active sizes, might be playing an important role in determining the magnitude of the climate impacts from volcanoes like Pinatubo.


2015 ◽  
Vol 15 (13) ◽  
pp. 19111-19160
Author(s):  
N. Bândă ◽  
M. Krol ◽  
M. van Weele ◽  
T. van Noije ◽  
P. Le Sager ◽  
...  

Abstract. The CH4 growth rate in the atmosphere showed large variations after the Pinatubo eruption in June 1991. A decrease of more than 10 ppb yr-1 in the growth rate over the course of 1992 was reported and a partial recovery in the following year. Although several reasons have been proposed to explain the evolution of CH4 after the eruption, their contributions to the observed variations are not yet resolved. CH4 is removed from the atmosphere by the reaction with tropospheric OH, which in turn is produced by O3 photolysis under UV radiation. The CH4 removal after the Pinatubo eruption might have been affected by changes in tropospheric UV levels due to the presence of stratospheric SO2 and sulfate aerosols, and due to enhanced ozone depletion on Pinatubo aerosols. The perturbed climate after the eruption also altered both sources and sinks of atmospheric CH4. Furthermore, CH4 concentrations were influenced by other factors of natural variability in that period, such as ENSO and biomass burning events. Emissions of CO, NOX and NMVOCs also affected CH4 concentrations indirectly by influencing tropospheric OH levels. Potential drivers of CH4 variability are investigated using the TM5 global chemistry model. The contribution that each driver had to the global CH4 variability during the period 1990 to 1995 is quantified. We find that a decrease of 8–10 ppb yr-1 CH4 is explained by a combination of the above processes. However, the timing of the minimum growth rate is found 6–9 months later than observed. The long-term decrease in CH4 growth rate over the period 1990 to 1995 is well captured and can be attributed to an increase in OH concentrations over this time period. Potential uncertainties in our modelled CH4 growth rate include emissions of CH4 from wetlands, biomass burning emissions of CH4 and other compounds, biogenic NMVOC and the sensitivity of OH to NMVOC emission changes. Two inventories are used for CH4 emissions from wetlands, ORCHIDEE and LPJ, to investigate the role of uncertainties in these emissions. Although the higher climate sensitivity of ORCHIDEE improves the simulated CH4 growth rate change after Pinatubo, none of the two inventories properly captures the observed CH4 variability in this period.


Science ◽  
1993 ◽  
Vol 259 (5100) ◽  
pp. 1411-1415 ◽  
Author(s):  
P. Minnis ◽  
E. F. Harrison ◽  
L. L. Stowe ◽  
G. G. Gibson ◽  
F. M. Denn ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document