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At least 1,567 records · Page 87
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NASA NTRS1978

Trace elemental characteristics of aerosols emitted from municipal incinerators

As part of a continuing investigation of high temperature combustion aerosols, elemental composition of size differentiated aerosols emitted from a local municipal incinerator was studied. Aerosols were aerodynamically separated into eight diameter groups ranging from 0.43 mm to 20 mm, collected, and analyzed by charged particle induced X-ray emission technique. On line data collection and reduction codes generated aerial densities for elements from Na to U with sensitivities in the ng/cu m range for most elements. From the total weights of aerosols collected per stage, their size distribution was determined to be bimodal, with one group centered at a diameter of 0.54 mm and the other at a diameter of 5.6 mm. Measured elemental concentrations in various size ranges indicate that K and S show a strong tendency to concentrate on aerosol surfaces. A weaker trend for surface preference was also observed for Mn and Ni, but other elements show no such trend.

Singh, J. J.↗
NASA NTRS1978

Albedo enhancement and perturbation of radiation balance due to stratospheric aerosols

The effect of stratospheric aerosols on the earth's monthly zonal radiation balance is investigated using a model layer consisting of 75% H2SO4, which is the primary constituent of the background aerosol layer. The reduction in solar energy absorbed by the earth-atmosphere system is determined through the albedo sensitivity, defined here as the change in albedo per unit mid-visible optical depth of the aerosol layer. The optically thin approximation is used in conjunction with the Henyey-Greenstein phase function for scattering to simplify computations. Satellite derived planetary albedos are used as the frame of reference about which the change in albedo is computed. An infrared radiative transfer model is used to estimate the increased greenhouse effect attributed to the aerosol layer. The infrared heating tends to compensate for the albedo effect in altering the radiation balance. The results indicate that the dominant influence of the thin model stratospheric aerosol layer is an increased reflection of solar energy all over the globe except for the polar-winter region, but the change in the radiation balance is seen to be uniform and small equatorwards of 50%.

HARSHVARDHAN↗
NASA NTRS1978

Post-volcanic stratospheric aerosol decay as measured by lidar

The paper summarizes and discusses results of lidar observations, at Hampton (Virginia), of the stratospheric aerosol vertical distribution for a period of 22 months (October 1974 to July 1976) after the volcanic eruption of the Volcan de Fuego in Guatemala. Data are presented in terms of lidar scattering ratio, vertically integrated aerosol backscattering, layer structure and location, and rawinsonde temperature profiles as a function of time. The results reveal a sudden increase in the stratospheric aerosol content after the volcanic eruption as well as its subsequent decline. There exists a high degree of correlation between the integrated aerosol backscattering and the tropopause height such that as one decreases the other increases and vice versa. Rapid decay of the stratospheric aerosol is found to occur over the late winter to early spring period.

Mccormick, M. P.↗
NASA NTRS1979

The investigation of advanced remote sensing techniques for the measurement of aerosol characteristics

Advanced remote sensing techniques and inversion methods for the measurement of characteristics of aerosol and gaseous species in the atmosphere were investigated. Of particular interest were the physical and chemical properties of aerosols, such as their size distribution, number concentration, and complex refractive index, and the vertical distribution of these properties on a local as well as global scale. Remote sensing techniques for monitoring of tropospheric aerosols were developed as well as satellite monitoring of upper tropospheric and stratospheric aerosols. Computer programs were developed for solving multiple scattering and radiative transfer problems, as well as inversion/retrieval problems. A necessary aspect of these efforts was to develop models of aerosol properties.

Deepak, A.↗
NASA NTRS1979

The NASA-Ames Research Center stratospheric aerosol model. 2. Sensitivity studies and comparison with observatories

Sensitivity tests were performed on a one-dimensional, physical-chemical model of the unperturbed stratospheric aerosols, and model calculations were compared with observations. The tests and comparisons suggest that coagulation controls the particle number mixing ratio, although the number of condensation nuclei at the tropopause and the diffusion coefficient at high altitudes are also important. The sulfur gas source strength and the aerosol residence time are much more important than the supply of condensation nuclei in establishing mass and large particle concentrations. The particle size is also controlled mainly by gas supply and residence time. In situ observations of the aerosols and laboratory measurements of aerosols, parameters that can provide further information about the physics and chemistry of the stratosphere and the aerosols found there are provided.

Toon, O. B.↗
NASA NTRS1979

Latitudinal variations of stratospheric aerosols

We have obtained stratospheric aerosols from tropical to northern latitudes using special collectors on U-2 aircraft during 1976 and 1977. Aerosols characterized by large numbers of small particles are found in the tropical zone suggesting this is a region of particle growth; whereas aerosols containing mostly larger particles are distributed throughout the Northern Hemisphere indicating a well-mixed, mature population. We find the aerosol layer extends from higher altitudes near the equator to lower ones toward the pole. Although this gradient suggests mature aerosols may leave the stratosphere at high latitudes, the data are, as yet, inconclusive. Comparisons of our data with those of other investigators using different instruments are generally encouraging, suggesting that if similar populations were sampled, the results would be similar. When our calculated sulfate mass mixing ratios are compared with those measured directly by others, we find better agreement is achieved if we assume more dilute sulfate and water mixtures than previously proposed.

Farlow, N. H.↗
NASA NTRS1980

Stratospheric aerosol modification by supersonic transport and space shuttle operations - Climate implications

The potential effects on stratospheric aerosols of supersonic transport emissions of sulfur dioxide gas and submicron soot granules, and space shuttle rocket emissions of aluminum oxide particulates are estimated. An interactive particle-gas model of the stratospheric aerosol layer is used to calculate changes due to exhaust emissions, and an accurate radiation transport model is employed to compute the effect of aerosol changes on the earth's average surface temperature. It is concluded that the release of large numbers of small particles (soot or aluminum oxide) into the stratosphere should not lead to a corresponding significant increase in the concentration of large, optically active aerosols, but that the increase in large particles is severely limited by the total mass of sulfate available to make large particles in situ, and by the rapid loss of small seed particles via coagulation. We find that a fleet of several hundred advanced supersonic aircraft operating daily at 20 km, or the launch of one space shuttle rocket per week, could produce roughly a 20% increase in the large-particle concentration of the stratosphere. We find, in addition, that aerosol increases of this magnitude would reduce the global surface temperature by less than 0.01 K.

Turco, R. P.↗
NASA NTRS1979

Formation and deposition of volcanic sulfate aerosols on Mars

The paper considers the formation and deposition of volcanic sulfate aerosols on Mars. The rate limiting step in sulfate aerosol formation on Mars is the gas phase oxidation of SO2 by chemical reactions with O, OH, and HO2; submicron aerosol particles would circuit Mars and then be removed from the atmosphere by gravitational forces, globally dispersed, and deposited over a range of equatorial and mid-latitudes. Volcanic sulfate aerosols on Mars consist of liquid droplets and slurries containing sulfuric acid; aerosol deposition on a global or hemispheric scale could account for the similar concentrations of sulfur within surficial soils at the two Viking lander sites.

Settle, M.↗
NASA NTRS1981

Measurements of the absorption coefficient of stratospheric aerosols

The absorption coefficients of stratospheric aerosols are measured using a variation on the integrating plate method. The technique is based on the decrease in the transparency of a substrate when an absorbing aerosol is deposited on it. A Lambert scatterer is placed behind the substrate to integrate forward scattered light and minimize the effect of scattering on the measurement. The low pressure in the stratosphere is used for the direct impaction of particles onto a narrow strip of opal glass. The eight samples collected had a median value of 4 x 10 to the -9th m with an uncertainty of + or - 5 x 10 to the -9th m. If this absorption is due to graphitic carbon, then its concentration is estimated at about 0.4 ng/cu m, or about 0.25% of the total aerosol mass concentration. Estimates of the aerosol scattering coefficients based on satellite extinction inversions result in an aerosol single-scattering albedo in the range of 0.96-1.0.

Ogren, J. A.↗
NASA NTRS1981

SAM 2 measurements of the polar stratospheric aerosol, volume 1: October to April 1979

Weekly averages of Antarctic and Arctic stratospheric aerosol data as well as corresponding temperature profiles for the time and place of each stratospheric aerosol measurement (SAM) II measurement during the first 6 months of satellite flight are presented. From the aerosol extinction profile data, contours of aerosol extinction as a function of altitude and longitude or time are plotted. Aerosol optical depths are calculated for each week. Polar stratospheric clouds at altitudes of about 22 km were observed during the Arctic winter at various times and locations. A representative sample of the first 6 months of data to be used in atmospheric and climatic studies is outlined.

Mccormick, M. P.↗
NASA NTRS1981

Aerosol generation and distribution system for the Third International Cloud Condensation Nuclei Workshop

In order to obtain identical samples participating CCN instruments and aerosol characterizing equipment were located along and connected to a 8.2 cm diameter aluminum tube through which the test aerosols were pumped directly from the source at very slight overpressure. Of the total of 29 experiments, 18 were carried out with artificial NaCl or (NH4)2SO4 aerosols. These were generated from salt solutions by pneumatic atomizers of special design to ensure high constancy of the aerosol output concentration. In three experiments with insoluble CCN (AgI, paraffin wax) the aerosols were generated thermally. In some of the tests, an electrostatic classifier was used for narrowing the particle size distributions.

Katz, U.↗
NASA NTRS1982

Altitude variations in stratospheric aerosols of a tropical region

To investigate the possibility that significant amounts of tropical tropospheric air may be convectively introduced into the stratosphere, aerosol samplings over Panama were made at various altitudes using a wire impactor collector. The percentage of particle sizes less than the mean mode decreases with height above the tropopause, suggesting depletion of small particles, possibly due to coagulation. Larger aerosols (greater than 0.3 micron in diam.) are more abundant farther above the tropopause, indicating growth, mainly by condensation. The total particle concentration decreases with increasing height above the tropopause, and also with increasing temperature. Aerosols containing smaller-size particles are thus found closer to the tropopause, and larger-size, more-evolved aerosols occur at higher altitudes. These data indicate that convective activity at the Intertropical Convergence Zone may be a source mechanism for stratospheric aerosols.

Goodman, J.↗
NASA NTRS1983

SAM 2 measurements of the polar stratospheric aerosol. Volume 4: April 1980 to October 1980

The Stratospheric Aerosol Measurement (SAM) 2 sensor is aboard the Nimbus 7 spacecraft providing extinction measurements of the Antarctic and Arctic stratospheric aerosols with a vertical resolution of 1 km. Representative examples and weekly averages of these aerosol data and corresponding temperature profiles are presented. Contours of aerosols extinction as a function of altitude and longitude or time are plotted and weekly aerosol optical depths are calculated. Stratospheric optical depths are 0.002 to 0.003 for the Antarctic and 0.002 to 0.003 at the beginning to 0.005 to 0.006 at the end of the time period for the Arctic. Polar stratospheric clouds at altitudes between the tropopause and 20 km were observed during the Antarctic winter. A ready-to-use format containing a representative sample of the fourth 6 months of data to be used in atmospheric and climatic studies is reported.

Mccormick, M. P.↗
NASA NTRS1983

Effect of the eruption of El Chichon stratospheric aerosol size and composition

Dominant effects of the El Chichon eruption on stratospheric aerosols at 19.8 to 20.7 km are: (1) vapor depositional growth of the small-aerosol (background) mode; (2) development of a large-particle mode by sedimentation from the highest altitudes in the cloud; (3) a change in the large-particle mode from sulfate-coated silicates to sulfate aerosols, some with silicate cores; (4) a 100-fold increase in sulfate mass in the large particle mode. Terminal velocities of large silicate particles, maximum r = 2.3 micron, sampled 1 month after eruption, and calibrated with the aid of lidar data, indicate initial injection to 26 to 27 km. Smaller velocities of sulfate aerosols, median r = 0.5 micron, are compatible with major growth in 2 to 3 months at 27 to 28 km. Aerosol settling accounts for the descent of the main lidar return to 26.5 km in August and to 20 to 21 km in December.

Oberbeck, V. R.↗
NASA NTRS1984

Climate studies with a multilayer energy balance model. III - Climatic impact of stratospheric volcanic aerosols

A multilayer energy balance model is applied in an examination of the sensitivity of climate to stratospheric aerosols induced by volcanic eruptions. Zonally and annually averaged quantities are considered, with ocean and land temperatures computed separately and the atmosphere below the 200 mb level divided into eight layers of 24 sublayers each. The aerosol is assumed to form in the 150-200 mb range. Aerosol parameters for radiative transfer calculations are reflection in the solar spectral region and absorption in the solar and IR regions. A 75 percent aqueous solution of sulfuric acid is assumed for the aerosols. The sensitivity of the hemispherically averaged surface temperature is enhanced 37 percent, with a 20 percent uncertainty, when the thermal IR radiation is excluded. The solar radiation enhances the surface temperatures to a higher degree than the thermal radiation. The maximum response to the evenly distributed aerosols is in the 60-70 deg N latitudes and propagates, weakening, to lower latitudes.

Chou, M.-D.↗
NASA NTRS1985

SAM 2 measurements of the polar stratospheric aerosol, volume 5

The Stratospheric Aerosol Measurement (SAM) 2 sensor is aboard the Earth-orbiting Nimbus 7 spacecraft providing extinction measurements of the Antarctic and Arctic stratospheric aerosol with a vertical resolution of 1 km. Representative examples and weekly averages of aerosol data and corresponding temperature profiles for the time and place of each SAM 2 mesurement (Oct. 1980 through Apr. 1981) are presented. Contours of aerosol extinction as a function of altitude and longitude or time are plotted and weekly aerosol optical depths are calculated. Seasonal variations and variations in space (altitude and longitude) for both polar regions are easily seen. Stratospheric optical depths are 0.002 to 0.003 for the Antarctic region and 0.005 to 0.006 at the beginning to 0.002 to 0.003 at the end of the time period for the Arctic region. The Northern Hemisphere values are quite large due mainly to the eruption of Mount St. Helens (46.2 deg N, 122.2 deg W) in May 1980. Polar stratospheric clouds at altitudes of about 20 km were observed during the Arctic winter. A ready-to-use format containing a representative sample of the fifth 6 months of data to be used in atmospheric and climatic studies is presented.

Mccormick, M. P.↗
NASA NTRS1985

SAM II measurements of the polar stratospheric aerosol. Volume 6: April to October 1981

The Stratospheric Aerosol Measurement (SAM) II sensor is aboard the Earth-orbiting Nimbus 7 spacecraft providing extinction measurements of the Antarctic and Arctic stratospheric aerosols with a vertical resolution of 1 km. Representative examples and weekly averages of these aerosol data and corresponding temperature profiles (Apr. 1981 to Oct. 1981) are presented. Contours of aerosol extinction as a function of altitude and longitude or time are plotted and weekly aerosol optical depths are calculated. Stratospheric optical depths are 0.002 to 0.003 for the Antarctic region and 0.006 to 0.007 at the beginning to 0.003 to 0.004 at the end of the time period for the Arctic region. Polar stratospheric clouds at altitudes between the tropopause and 20 km were observed during the Antarctic winter. A ready-to-use format containing a representative sample of the sixth 6 months of data to be used in atmospheric and climatic studies is reported.

Mccormick, M. P.↗
NASA NTRS1985

Influence of meteorological conditions on aerosol vertical distribution and composition off the northeast American coastline

The size distribution and composition of lower tropospheric aerosols were measured off the northeast American coastline under clear air and disturbed meteorological conditions. Under the clear air conditions observed on 5 August 1982, with air flow from west to east, sulfate-rich stratified layers are the dominant feature of aerosol distribution in the lowest 3000 m of the troposphere. The encroachment of a warm frontal system over the study area on 9 August 1982 resulted in dramatic changes in aerosol distribution and composition prior to any precipitation, probably due to increased vertical mixing and dilution of pollutant aerosols. Chloride becomes the dominant water soluble anion in the lower 3000 m, primarily due to a several fold decrease in sulfate. Although these results are limited to only two sets of measurements, the data indicate the variability which can occur in the tropospheric vertical aerosol distributions at remote locations. A knowledge of the structure and stability of these stratified layers is of particular importance to studies of the ocean-troposphere chemistry problem.

Sebacher, D. I.↗