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Global to Microscale Evolution of the Pinatubo Volcanic Aerosol Derived from Diverse Measurements and AnalysesWe assemble data on the Pinatubo aerosol from space, air, and ground measurements, develop a composite picture, and assess the consistency and uncertainties of measurement and retrieval techniques. Satellite infrared spectroscopy, particle morphology, and evaporation temperature measurements agree with theoretical calculations in showing a dominant composition of H2SO4-H20 mixture, with H2SO4 weight fraction of 65-80% for most stratospheric temperatures and humidities. Important exceptions are (1) volcanic ash, present at all heights initially and just above the tropopause until at least March 1992, and (2) much smaller H2SO4 fractions at the low temperatures of high-latitude winters and the tropical tropopause. Laboratory spectroscopy and calculations yield wavelength- and temperature-dependent refractive indices for the H2SO4-H20 droplets. These permit derivation of particle size information from measured optical depth spectra, for comparison to impactor and optical-counter measurements. All three techniques paint a generally consistent picture of the evolution of R(sub eff), the effective radius. In the first month after the eruption, although particle numbers increased greatly, R(sub eff) outside the tropical core was similar to preeruption values of approx. 0.1 to 0.2 microns, because numbers of both small (r < 0.2 microns) and large (r > 0.6 microns) particles increased. In the next 3-6 months, extracore R(sub eff) increased to approx. 0.5 microns, reflecting particle growth through condensation and coagulation. Most data show that R(sub eff) continued to increase for about 1 year after the eruption. R(sub eff) values up to 0.6 - 0.8 microns or more are consistent with 0.38 - 1 micron optical depth spectra in middle to late 1992 and even later. However, in this period, values from in situ measurements are somewhat less. The difference might reflect in situ undersampling of the very few largest particles, insensitivity of optical depth spectra to the smallest particles, or the inability of flat spectra to place an upper limit on particle size. Optical depth spectra extending to wavelengths lambda > 1 micron are required to better constrain R(sub eff), especially for R(sub eff) > 0.4 microns. Extinction spectra computed from in situ size distributions are consistent with optical depth measurements; both show initial spectra with lambda(sub max) <= 0.42 microns, thereafter increasing to 0.78 <= lambda(sub max) <= 1 micron. Not until 1993 do spectra begin to show a clear return to the preeruption signature of lambda(sub max) <= 0.42 microns. The twin signatures of large R(sub eff) (> 0.3 microns) and relatively flat extinction spectra (0.4 - 1 microns) are among the longest-lived indicators of Pinatubo volcanic influence. They persist for years after the peaks in number, mass, surface area, and optical depth at all wavelengths <= 1 microns. This coupled evolution in particle size distribution and optical depth spectra helps explain the relationship between global maps of 0.5- and 1.0-micron optical depth derived from the Advanced Very High Resolution Radiometer (AVHRR) and Stratospheric Aerosol and Gas Experiment (SAGE) satellite sensors. However, there are important differences between the AVHRR and SAGE midvisible optical thickness products. We discuss possible reasons for these differences and how they might be resolved.
Document ID
20000052535
Acquisition Source
Ames Research Center
Document Type
Reprint (Version printed in journal)
Authors
Russell, P. B.
(NASA Ames Research Center Moffett Field, CA United States)
Livingston, J. M.
(SRI International Corp. Menlo Park, CA United States)
Pueschel, R. F.
(NASA Ames Research Center Moffett Field, CA United States)
Bauman, J. J.
(State Univ. of New York Stony Brook, NY United States)
Pollack, J. B.
(NASA Ames Research Center Moffett Field, CA United States)
Brooks, S. L.
(Synernet Corp. Fremont, CA United States)
Hamill, P.
(San Jose State Univ. CA United States)
Thomason, L. W.
(NASA Langley Research Center Hampton, VA United States)
Stowe, L. L.
(National Environmental Satellite Service Washington, DC United States)
Deshler, T.
(Wyoming Univ. Laramie, WY United States)
Dutton, E. G.
(National Oceanic and Atmospheric Administration Boulder, CO United States)
Bergstrom, Robert W.
(Bay Area Environmental Research Inst. San Francisco, CA United States)
Date Acquired
August 19, 2013
Publication Date
February 28, 2000
Publication Information
Publication: Analysis of Atmospheric Aerosol Data Sets and Application of Radiative Transfer Models to Compute Aerosol Effects
Subject Category
Environment Pollution
Report/Patent Number
Paper 96JD01162
Distribution Limits
Public
Copyright
Other

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