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At least 685 records · Page 38

Stratospheric aerosols in the intertropical convergence zone, Panama Canal zone

To investigate whether injection sources of the stratospheric aerosol layer could be detected in the tropical stratosphere, an examination of the aerosol vertical and horizontal size distribution around the Intertropical Convergence Zone (ITCZ) at the Panama Canal Zone was performed during the summer of 1977. By comparing these data with similar measurements in temperate and polar regions, it was hoped to discover variations in particle size that would indicate whether a young aerosol is forming and entering the stratosphere at the ITCZ; where the aerosol matures; and finally, where it reenters the troposphere. The methods used in the investigations and the results obtained from the analyses are described.

Farlow, N. H.↗

Effect of the reaction HO2 + O3 yields OH + 2O2 on stratospheric ozone

It is noted that recent measurements of large values of the rate coefficient for the reaction NO + HO2 yields NO2 + OH lead to model predictions of excessive amounts of stratospheric ozone. This letter shows that a recent measurement of the rate coefficient (k2) for the reaction HO2 + O3 yields OH + 2O2 largely resolves these problems of excessive stratospheric ozone in models. A two-dimensional model of stratospheric trace constituents is used to calculate the concentrations of 35 constituents; the results are compared with experimental measurements of ozone column densities. It is found that the model predictions of excess ozone abundances diminish significantly when the measured value of k2 is employed.

Whitten, R. C.↗

The reaction Cl + H2CO yields HCl + HCO: Decreased sensitivity of stratospheric ozone to chlorine perturbations

The absolute rate constant for the reaction Cl + H2CO yields HCl + HCO has been determined by the flash-photolysis-resonance fluorescence method to be + or - 0.9 (2 sigma) x 10 to the -11th power cu cm/molecule per sec at 298 K and to have a negligible temperature dependence. This rate, which at stratospheric temperatures is more than 2000 times faster than the rate of Cl + CH4 and more than a factor of 2 faster than Cl + HO2, indicates that formaldehyde (H2CO) will compete significantly with methane (CH4) and HO2 for the conversion of active chlorine in the stratosphere to the inactive reservoir HCl. Chlorine will thus be a less efficient destroyer of stratospheric ozone than previously believed. One-dimensional eddy-diffusion photochemical model calculations indicate that the eventual ozone depletion for a steady-state chlorfluoromethane release at 1975 rates (750,000 tons/year) will be lowered from 20% to 18.5% by the inclusion of this reaction.

Stief, L. J.↗

Stratospheric-related research using the shock tube

The capabilities of shock tubes used in stratospheric-related research are considered, and the results of three independent shock tube research projects are reported. The studies are concerned with the evaluation of stratospheric ozone depletion. In the first experiment, photoabsorption cross sections of Freon 11 and 12 at stratospheric temperatures were measured using rarefaction waves. In the second experiment, reaction-rate coefficients were determined from measurements made behind reflected shock waves. In the third experiment, electronic-transition moments of the O2 Schumann-Runge system and the A2Pi-X2Pi system of ClO were deduced from intensity measurements made behind the incident shock.

Cooper, D. M.↗

COS in the stratosphere

Carbonyl sulfide (COS) has been detected in the stratosphere, and mixing ratio measurements are reported for altitudes of 15.2 to 31.2 km. A large volume, cryogenic sampling system mounted on board a U-2 aircraft has been used for lower stratosphere measurements and a balloon platform for measurement at 31.2 km. These observations and measurements strongly support the concept that stratospheric COS is an important precursor in the formation of sulfuric acid aerosols.

Inn, E. C. Y.↗

The behavior of tropical ozone during the stratospheric warming of March-April 1976

The backscatter ultraviolet spectrometer on the Atmosphere Explorer-E satellite obtained ozone data for the upper stratosphere and lower mesosphere from an equatorial orbit near the time of the March-April 1976 stratospheric warming. A simple inversion technique allows the extraction of information on the absolute ozone abundance and its longitudinal variation from the measured radiances. Between altitudes of 35 and 60 km tropical O3 in constant pressure layers exhibits increased spatial variations on length scales of 20 to 30 deg in longitude after the onset of the polar warming, indicating enhanced wave activity. One week after the polar vortex breakdown, upper stratospheric O3 begins a relaxation toward the unperturbed state, while that in the lower mesosphere continues to show maximum variations near + or 10% of the longitudinally averaged value. Although the degree of horizontal structure increases during the warming, the absolute O3 amounts averaged over longitude between 35 and 60 km in altitude remain nearly constant in time. The observed behavior is consistent with that expected from enhanced vertical transport of O3 in the tropics with accompanying adiabatic temperature changes which alter the chemical loss rate.

Frederick, J. E.↗

Comparison of seasonal variations of upper stratospheric ozone concentrations revealed by Umkehr and Nimbus 4 BUV observations

This paper reports the results of a comparison between upper stratospheric ozone concentration profiles in the region between 22 and 1.4 mbar, as determined from surface-based Umkehr observations and satellite Nimbus 4 BUV observations. The Umkehr data, consisting of monthly averages of observations extending over several years or longer, were obtained at three stations located in the Northern Hemisphere and two in the Southern Hemisphere. The BUV data were obtained during the period from May 1970 to March 1971. Aside from some bias in the magnitudes of the Umkehr and BUV data, marked annual cycles of ozone concentration in the upper stratosphere are clearly revealed. Above 4 mbar the profiles show a summer minimum and a winter maximum, while below 4 mbar the annual variation is reversed from this pattern. In the Northern Hemisphere the winter maximum is accompanied by a secondary minimum of 1- to 2-month duration near 3 mbar. This short-term minimum is much less obvious in the Southern Hemisphere data. Some of the problem of attempting to monitor long-term changes in the upper stratosphere are discussed briefly.

Deluisi, J. J.↗

Minor constituents in the stratosphere and mesosphere

A review of the research in minor constituents in the stratosphere and mesosphere, carried out between 1975 and 1978, is presented. Much of the theoretical research was done with the aid of one-dimensional models. Different aspects of these models are discussed. Measurements of the chlorofluoromethanes, hydrochloric acid, nitric oxide, nitrous oxide, and hydrogen oxide were conducted. It is noted that the hydrogen oxides are now assuming a larger role in stratospheric photochemistry than have been postulated before. The effect of water vapor and the hydrogen oxides on the overall chemistry of the stratosphere was investigated theoretically, along with the possible relationship between solar activity and atmospheric ozone. The mesosphere study included ozone, water vapor, nitric oxide, and odd nitrogen investigations.

Hudson, R. D.↗

Stratospheric aerosol modification by supersonic transport operations with climate implications

The potential effects on stratospheric aerosois of supersonic transport emissions of sulfur dioxide gas and submicron size soot granules are estimated. An interactive particle-gas model of the stratospheric aerosol is used to compute particle changes due to exhaust emissions, and an accurate radiation transport model is used to compute the attendant surface temperature changes. It is shown that a fleet of several hundred supersonic aircraft, operating daily at 20 km, could produce about a 20% increase in the concentration of large particles in the stratosphere. Aerosol increases of this magnitude would reduce the global surface temperature by less than 0.01 K.

Toon, O. B.↗

Aircraft search for millimeter-wavelength emission by stratospheric ClO

Three millimeter-wavelength transitions of ClO were searched for in the stratospheric emission spectrum during May-August 1977 using aircraft-based instruments. The measurements indicate that if stratospheric ClO has a vertical distribution of the form predicted by present photochemical models, then the ClO volume mixing ratio at the profile peak did not exceed 10 to the -9th at the time and place of the measurements. The observed spectra suggest the presence of ClO in the stratosphere but do not provide a definitive detection.

Waters, J. W.↗

Possible existence and chemistry of ClO.O2 in the stratosphere

The influence of the existence and chemistry of the possible atmospheric constituent ClO.O2 on current models of stratospheric photochemistry is discussed. It is suggested that the formation of an asymmetric ClO.O2 complex may explain the observed suppression of the quantum yield in the chlorine-photosensitized decomposition of ozone in the presence of O2, and that the presence of the ClO.O2 formed may account for the current discrepancy between measurements and theoretical predictions of stratospheric ClO mixing ratio profiles. The presence of stratospheric ClO.O2 is also invoked as a possible mitigating influence on present estimates of ozone destruction due to chlorofluoromethane release.

Prasad, S. S.↗

Rocket observations of the vertical distribution of ozone in the polar night and during a mid-winter stratospheric warming

Rocket ozone soundings have been conducted in the stratosphere and lower mesosphere at high latitudes during winter. The collection of soundings show a high degree of variability when compared to ozone distributions measured during summer and at lower latitudes. The concurrently observed temperature and winds also show large variations which can be qualitatively related to the ozone profiles. Two most unusual ozone profiles were observed in January 1979 over Alaska during a stratospheric warming event. Both ozone profiles were consistent in showing the measured mixing ratios to be higher at 50 km than those measured at 40 km, a feature never reported before. This feature is related to the concurrently observed wind and temperature distributions and the NMC analyses of pressure height fields. The polar night ozone observations in the upper stratosphere and lower mesosphere suggest some temperature dependence, but transports seem to play an important role.

Hilsenrath, E.↗

A search for correlation between geomagnetic activity and stratospheric ozone

The total ozone column content (TOZ) measured from the Nimbus 4 BUV experiment is analyzed in geomagnetic coordinates to study a possible link between the solar corpuscular radiation and the lower stratosphere. Using planetary magnetic index Ap as a measure of the solar corpuscular radiation, it is shown that the correlation between TOZ and Ap, if any, occurs predominantly at high latitudes during winter seasons. This is typical of most of the claimed correlations between sun and weather and may be the result of the winter increase of planetary wave activity which by coincidence have periods comparable to magnetic activity. The fact that even major magnetic storms have no detectable effect on the stratospheric ozone during summer does not support a direct cause and effect relation between solar and stratospheric perturbations.

Chandra, S.↗

Size distributions and mineralogy of ash particles in the stratosphere from eruptions of Mount St. Helens

Samples from the stratosphere obtained by U-2 aircraft after the first three major eruptions of Mount St. Helens contained large globules of liquid acid and ash. Because of their large size, these globules had disappeared from the lower stratosphere by late June 1980, leaving behind only smaller acid droplets. Particle size distributions and mineralogy of the stratospheric ash grains demonstrate inhomogeneity in the eruption clouds.

Farlow, N. H.↗

A study of stratospheric aerosol maturity

A sampling and analysis technique that uses the binomial distribution to characterize stratospheric aerosol populations at the 95% level of confidence is described. Particle samples obtained over Alaska during July 15-19, 1979, are used; the results show the presence of more small particles at lower altitude than at high altitudes. Calculations of the surface area and volume distributions for all aerosol samples collected are given. Evidence from these data suggests either that Aitken nuclei are injected or diffused across the tropopause and rise into the stratosphere, where they mature into larger particles, or nuclei form in the lower stratosphere and become mature aerosols at high altitude. Samples obtained at another site give the same results, supporting the view that the process of injection or nucleation and maturing of aerosols with altitude may be global and need not occur only in locations exhibiting unique meteorologic features.

Oberbeck, V. R.↗

Radiative properties of the background stratospheric aerosols and implications for perturbed conditions

A series of Mie scattering calculations has been performed to define the wavelength-dependent, single scattering properties of aerosols present in the stratosphere during July 1979. Additional radiative transfer computations were conducted to assess the impact of aerosols on the earth's radiation budget. For these purposes, an extensive set of measurements of aerosol characteristics that were obtained in Alaska from aircraft and satellite platforms was used. At that time, the optical depth was too small for aerosols to significantly impact earth's climate. But the optical depth of the stratospheric aerosol layer has been large enough during some volcanically perturbed periods for the aerosols to have caused a noticeable warming of the stratosphere and cooling of the troposphere.

Pollack, J. R.↗

Stratospheric hydroxyl radical concentrations - New limitations suggested by observations of gaseous and particulate sulfur

A one-dimensional aerosol model is employed in investigating the sensitivity of the stratospheric distributions of gaseous sulfur compounds and sulfate aerosol particles to changes in OH and CS2 concentrations, in eddy diffusion coefficients, and in important chemical rate constants. By comparing model predictions with recent observational data for SO2, OCS, and particulates, it is found that, with regard to atmospheric sulfur, CS2 is only a secondary source of sulfur for the stratosphere relative to OCS and that background tropospheric CS2 concentrations by volume are likely to be less than 70 parts per trillion. It is also established that under stratospheric conditions the rate coefficients for the reactions of OH with OCS and CS2 may be substantially smaller than the room temperature laboratory values of Kurylo (1978).

Turco, R. P.↗

Numerical simulation of stratospheric sudden warmings with a primitive equation spectral model

A 26-level primitive equation spherical harmonic spectral model allowing for wave-wave and wave-zonal flow interactions is presented for the study of stratospheric sudden warmings. The warmings are simulated by the forcing of a single planetary wave at the tropopause. Four numerical experiments were performed. Nonlinear wave-wave interactions appear to play an important role in the evolution of the flow and temperature fields in the middle to upper stratosphere. In the case involving both wave-wave and wave-zonal flow interactions, this was manifested by the split in the initial polar vortex into a quasi-wave number 2 pattern. In the cases at 60 deg N, easterlies develop first in the upper mesosphere and descend gradually. About the same time or a little later, easterlies also develop in the mid-stratosphere. The linear cases exhibit warmings which are more shallow and more intense at 30 km than the nonlinear cases.

Lordi, N. J.↗