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El Chichon volcanic aerosols: Impact of radiative, thermal, and chemical perturbations
Author(s) -
Michelangeli Diane V.,
Allen Mark,
Yung Yuk L.
Publication year - 1989
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/jd094id15p18429
Subject(s) - photodissociation , radiative transfer , aerosol , volcano , atmospheric sciences , reaction rate constant , stratosphere , wavelength , chemistry , photochemistry , physics , meteorology , kinetics , geology , optics , quantum mechanics , seismology
We examine the consequences of the eruption of the El Chichon volcano on the Earth's stratospheric chemistry. Formed after the eruption, the volcanic aerosol cloud, with a peak particle density at 27 km, was very efficient at altering the radiation field. The results of a one‐dimensional radiative transfer model show that the total radiation increased by 8% within the aerosol layer longward of 3000 Å. At certain altitudes and wavelengths below 3000 Å, the total radiation decreased by 15%. Consequently, there are changes in the photolysis rates obtained with a one‐dimensional photochemical model: for example, O 2 photodissociation rate constants decrease by 10%, while O 3 photodissociation rate constants increase by a comparable amount. A combination of this radiation change and the effect of a temperature variation of a few degrees causes the abundance of O 3 to decrease by 7% at 24 km, in good agreement with the Solar Backscattered Ultraviolet experiment (SBUV) measurements of a 5–10% decrease. The combined radiative and thermal perturbations on the concentrations of O, O( 1 D ), OH, HO 2 , H 2 O 2 , NO, NO 2 , NO 3 , N 2 O 5 , HNO 3 , HO 2 NO 2 , Cl, ClO, ClO 2 , HOCl, ClNO 3 , and HCl are computed and presented in detail. However, these changes as calculated are insufficient to explain the observations of significant decreases in NO and NO 2 and increases in HCl. A heterogeneous reaction catalyzed by aerosol surfaces which transforms ClNO 3 into HCl provides a pathway for sequestering NO x , and at the same time reduces ClNO 3 in favor of HCl. The inclusion of this reaction in the model leads to a satisfactory single‐step explanation of the otherwise puzzling observations of NO, NO 2 , and HCl. The observed lack of change in HNO 3 cannot be explained by this hypothesis. The effects of a number of heterogenous reactions, some believed to be important for the Antarctic stratosphere, have been assessed with our model. We also examine the hypothesis of direct injection of gases from the volcano into the stratosphere. Only an unrealistically large injection (60% column increase above 12 km) results in an HCl increase in agreement with observations. An equally large water injection decreases HCl, and decreases the NO and NO 2 by as much as 20%, but still does not simulate the observed NO x decrease.

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