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Sebacher, D. I.

Publications and source records attributed to Sebacher, D. I..

At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS2000

BOREAS TGB-5 Biogenic Soil Emissions of NO and N2O

The BOReal Ecosystem-Atmosphere Study Trace Gas Biogeochemistry (BOREAS TGB)-5 team made several measurements of trace gas concentrations and fluxes at various NSA sites. This data set contains biogenic soil emissions of nitric oxide and nitrous oxide that were measured over a wide range of spatial and temporal site parameters. Since very little is known about biogenic soil emissions of nitric oxide and nitrous oxide from the boreal forest, the goal of the measurements was to characterize the biogenic soil fluxes of nitric oxide and nitrous oxide from black spruce and jack pine areas in the boreal forest. The diurnal variation and monthly variation of the emissions was examined as well as the impact of wetting through natural or artificial means. Temporally, the data cover mid-August 1993, June to August 1994, and mid-July 1995. The data are provided in tabular ASCII files. The data files are available on a CD-ROM (see document number 20010000884).

Levine, J. S.↗
NASA NTRS1986

Evaluation of standard radiation atmosphere aerosol models for a coastal environment

Calculations are compared with data from an experiment to evaluate the utility of standard radiation atmosphere (SRA) models for defining aerosol properties in atmospheric radiation computations. Initial calculations with only SRA aerosols in a four-layer atmospheric column simulation allowed a sensitivity study and the detection of spectral trends in optical depth, which differed from measurements. Subsequently, a more detailed analysis provided a revision in the stratospheric layer, which brought calculations in line with both optical depth and skylight radiance data. The simulation procedure allows determination of which atmospheric layers influence both downwelling and upwelling radiation spectra.

Whitlock, C. H.↗
NASA NTRS1986

Air chemistry over the tropical forest of Guyana

A comparison is made of the atmospheric chemistry within and above the atmospheric boundary layer over the tropical forest of Guyana. The data were gathered by NASA during the Global Tropospheric Experiment program in 1984, with an instrumented aircraft being used to collect data at altitudes of 3.5 km and between 150-450 m. The synoptic data covered concentrations of O3, CO, dimethylsulfide (DMS), halocarbons and isoprene and three different aerosol particulate measurements (DIAL system). The forest boundary layer proved to be a significant sink for O3, and a source for substantial emissions of DMS. Isoprene emitted by the forest was photochemically oxidized and became a source of CO.

Gregory, G. L.↗
NASA NTRS1986

Distribution and geochemistry of aerosols in the tropical North Atlantic troposphere - Relationship to Saharan dust

Estimates of global aerosol production suggest that mobilization of natural eolian material greatly exceeds anthropogenic-related emissions, and it appears that soil material transported from arid regions by wind might be mainly responsible for the distribution of certain clay materials in oceanic sediments. In connection with studies related to an investigation of these possibilities, the present paper provides a discussion of the aerosol spatial distribution and its water-soluble chemical composition in the tropical North Atlantic troposphere during the ABLE-Barbados mission. Particular attention is given to the composition of the water-soluble fraction, since its chemical reactivity is important with respect to various atmospheric and biogeochemical processes. On the basis of the obtained results, it is suggested that Saharan dust has also a significant impact on the aerosol chemistry over the tropical North Atlantic.

Talbot, R. W.↗
NASA NTRS1986

Atmospheric methane sources - Alaskan tundra bogs, an alpine fen, and a subarctic boreal marsh

Methane (CH4) flux measurements from Alaska tundra bogs, an alpine fen, and a subarctic boreal marsh were obtained at field sites ranging from Prudhoe Bay on the coast of the Arctic Ocean to the Alaskan Range south of Fairbanks during August 1984. In the tundra, average CH4 emission rates varied from 4.9 mg CH4 per sq m per day (moist tundra) to 119 mg CH4 per sq m per day (waterlogged tundra). Fluxes averaged 40 mg CH4 per sq m per day from wet tussock meadows in the Brooks Range and 289 mg Ch4 per sq m per day from an alpine fen in the Alaskan Range. The boreal marsh had an average CH4 emission rate of 106 mg CH4 per sq m per day. Significant emissions were detected in tundra areas where peat temperatures were as low as 4 C, and permafrost was only 25 cm below the ground surface. Emission rates from the 17 sites sampled were found to be logarithmically related to water levels at the sites. Extrapolation of the data to an estimate of the total annual CH4 emission from all arctic and boreal wetlands suggests that these ecosystems are a major source of atmospheric CH4 and could account for up to 23 percent of global CH4 emissions from wetlands.

Sebacher, D. I.↗
NASA NTRS1985

Sources of atmospheric methane from wetlands

Through the use of a computerized Geographic Information Service (GIS), field data on methane emissions and water inundation levels have been combined with remotely sensed vegetation cover data. This permits a more precise extrapolation of point flux measurements to regional scale flux estimates. Since the GIS allows changes in environmental variables to be included in the model, the sensitivity of emissions on large scales to changes in these parameters may be studied. Here, methane flux measurements from the Everglades marsh complex are reported, giving the flux by vegetation class.

Bartlett, K. B.↗
NASA NTRS1985

Methane flux from coastal salt marshes

It is thought that biological methanogenesis in natural and agricultural wetlands and enteric fermentation in animals are the dominant sources of global tropospheric methane. It is pointed out that the anaerobic soils and sediments, where methanogenesis occurs, predominate in coastal marine wetlands. Coastal marine wetlands are generally believed to be approximately equal in area to freshwater wetlands. For this reason, coastal marine wetlands may be a globally significant source of atmospheric methane. The present investigation is concerned with the results of a study of direct measurements of methane fluxes to the atmosphere from salt marsh soils and of indirect determinations of fluxes from tidal creek waters. In addition, measurements of methane distributions in coastal marine wetland sediments and water are presented. The results of the investigation suggest that marine wetlands provide only a minor contribution to atmospheric methane on a global scale.

Bartlett, K. B.↗
NASA NTRS1985

Methane emissions to the atmosphere through aquatic plants

The movement of methane (CH4) from anaerobic sediments through the leaves, stems, and flowers of aquatic plants and into the atmosphere was found to provide a significant pathway for the emission of CH4 from the aquatic substrates of flooded wetlands. Methane concentrations well above the surrounding ambient air levels were found in the mesophyll of 16 varies of aquatic plants and are attributed to transpiration, diffusion, and pressure-induced flow of gaseous CH4 from the roots when they are embedded in CH4-saturated anaerobic sediments. Methane emissions from the emergent parts of aquatic plants were measured using floating chamber techniques and by enclosing the plants in polyethylene bags of known volume. Concentration changes were monitored in the trapped air using syringes and gas chromatographic techniques. Vertical profiles of dissolved CH4 in sediment pore water surrounding the aquatic plants' rhizomes were obtained using an interstitial sampling technique. Methane emissions from the aquatic plants studied varied from 14.8 mg CH4/d to levels too low to be detectable. Rooted and unrooted freshwater aquatic plants were studied as well as saltwater and brackish water plants. Included in the experiment is detailed set of measurements on CH4 emissions from the common cattail (Typha latifolia). This paper illustrates that aquatic plants play an important gas exchange role in the C cycle between wetlands and the atmosphere.

Sebacher, D. I.↗
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.↗
NASA NTRS1984

Surface chloride salt formation on Space Shuttle exhaust alumina

Aluminum oxide samples from the exhaust of Space Shuttle launches STS-1, STS-4, STS-5, and STS-6 were collected from surfaces on or around the launch pad complex and chemically analyzed. The results indicate that the particulate solid-propellant rocket motor (SRM) alumina was heavily chlorided. Concentrations of water-soluble aluminum (III) ion were large, suggesting that the surface of the SRM alumina particles was rendered soluble by prior reactions with HCl and H2O in the SRM exhaust cloud. These results suggest that Space Shuttle exhaust alumina particles are good sites for nucleation and condensation of atmospheric water. Laboratory experiments conducted at 220 C suggest that partial surface chloriding of alumina may occur in hot Space Shuttle exhaust plumes.

Cofer, W. R., III↗
NASA NTRS1984

Atmospheric transport of pollutants from North America to the North Atlantic Ocean

Ground-based measurements strongly support the hypothesis that pollutant materials of anthropogenic origin are being transported over long distances in the midtroposphere and are a significant source of acid rain, acid snow, trace metal deposition, ozone and visibility-reducing aerosols in remote oceanic and polar regions of the Norhern Hemisphere. Atmospheric sulphur budget calculations and studies of acid rain on Bermuda indicate that a large fraction of pollutant materials emitted into the atmosphere in eastern North America are advected eastwards over the North Atlantic Ocean. The first direct airborne measurements of the vertical distribution of tropospheric aerosols over the western North Atlantic is reported here. A newly developed airborne differential adsorption lidar system was used to obtain continuous, remotely sensed aerosol distributions along its flight path. The data document two episodes of long-distance transport of pollutant materials from North America over the North Atlantic Ocean.

Harriss, R. C.↗
NASA NTRS1984

Airborne measurements of launch vehicle effluent of STS-2 launch on November 12, 1981 at Cape Canaveral, Florida

The second Space Shuttle (STS-2) was launched from the John F. Kennedy Space Center at 1010 EST on November 12, 1981. An instrumented light airplane was used to measure the emitted concentration of Shuttle exhaust products produced during launch. The airplane accomplished 31 passes through and under the exhaust cloud in the 1 hr 45 min immediately following the launch. Measurements included the following: (1) particulate data in the form of a light scattering coefficient obtained from an integrating nephelometer, (2) particulate concentrations and mass concentrations obtained from a spectrometer probe, (3) gaseous HCl and total HCl concentrations obtained from a gas-filter-correlation instrument and a chemiluminescent instrument, respectively, and (4) outside-air temperature and dew-point temperature. These data are presented along with time, altitude, and position for each cloud pass. These data are within the range of values observed during similar measurements made during the first Space Shuttle launch on April 12, 1981.

Maddrea, G. L., Jr.↗
NASA NTRS1984

Hydrogen chloride and aerosol ground cloud characteristics resulting from Space Shuttle launches

Airborne measurements of gaseous HCl, gaseous and aerosol HCl, particulates, relative humidity and temperature were obtained in ground clouds produced during three Space Shuttle launches. Partitioning of HCl between HCl aerosol and gaseous HCl was investigated as the solid rocket exhaust cloud diluted with ambient air to evaluate the conditions under which aerosol formation occurs in the troposphere in the presence of hygroscopic HCl vapor. Equilibrium predictions for aqueous HCl aerosol formation generally agree with the measured HCl partitioning over HCl concentrations from 0.5 to 36 ppm. HCl concentration dispersion within four cloud segments at time t (min) was evaluated using the expression C = C(0) (t to the alpha power) where C(0) varied from 145 to 2250 ppm and alpha varied from -1.14 to -1.73. Aerosol fallout from the exhaust clouds was measured with time by monitoring HCl concentrations and aerosol distributions 100 m below the cloud as it drifted away from the launch site. Significant amounts of HCl were found to be removed by fallout of particles in the 80-220 micron diameter range up to 30 min after launch.

Sebacher, D. I.↗
NASA NTRS1983

Methane flux across the air-water interface - Air velocity effects

Methane loss to the atmosphere from flooded wetlands is influenced by the degree of supersaturation and wind stress at the water surface. Measurements in freshwater ponds in the St. Marks Wildlife Refuge, Florida, demonstrated that for the combined variability of CH4 concentrations in surface water and air velocity over the water surface, CH4 flux varied from 0.01 to 1.22 g/sq m/day. The liquid exchange coefficient for a two-layer model of the gas-liquid interface was calculated as 1.7 cm/h for CH4 at air velocity of zero and as 1.1 + 1.2 v to the 1.96th power cm/h for air velocities from 1.4 to 3.5 m/s and water temperatures of 20 C.

Sebacher, D. I.↗
NASA NTRS1983

HCl in rocket exhaust clouds - Atmospheric dispersion, acid aerosol characteristics, and acid rain deposition

Both measurements and model calculations of the temporal dispersion of peak HCl (g + aq) concentration in Titan III exhaust clouds are found to be well characterized by one-term power-law decay expressions. The respective coefficients and decay exponents, however, are found to vary widely with meteorology. The HCl (g), HCl (g + aq), dewpoint, and temperature-pressure-altitude data for Titan III exhaust clouds are consistent with accurately calculated HCl/H2O vapor-liquid compositions for a model quasi-equilibrated flat surface aqueous aerosol. Some cloud evolution characteristics are also defined. Rapid and extensive condensation of aqueous acid clearly occurs during the first three min of cloud rise. Condensation is found to be intensified by the initial entrainment of relatively moist ambient air from lower levels, that is, from levels below eventual cloud stabilization. It is pointed out that if subsequent dilution air at stabilization altitude is significantly drier, a state of maximum condensation soon occurs, followed by an aerosol evaporation phase.

Pellett, G. L.↗
NASA NTRS1983

Airborne measurements of launch vehicle effluent: Launch of Space Shuttle (STS-1) on 12 April 1981

Launch vehicle effluent environmental impact activities from the first space shuttle (STS-1) included airborne measurements within the exhaust cloud from about 9 min after launch (T + 9) to T + 120 min. Measurements included total hydrogen chloride (gaseous plus aqueous) concentrations, particulate concentrations, temperature, and dewpoint temperature. The airborne measurements are summarized. The physical growth and behavior of exhaust clouds is presented as well as the results of laboratory analysis of elemental composition of particulate samples collected by the aircraft. Observed results from the STS-1 launch are compared with earlier Titan III results. Shuttle effluent concentrations are found to be within the range of Titan III observations.

Gregory, G. L.↗
NASA NTRS1983

Airborne measurements of Space Shuttle exhaust constituents

Airborne measurements of hydrogen chloride (HCl) and particulates made during penetrations into and flights under Space Shuttle exhaust clouds from launches STS-1, -2, and -5 are presented to permit comparison with dispersion model predictions for Space Shuttle exhaust clouds, and with previous measurements made in Titan III exhaust clouds. Analytical techniques employed for the Shuttle measurements were developed and refined during earlier Titan III exhaust cloud measurements and include the measurements of particulate concentrations, size distributions, and the partitioning of HCl between the gaseous and aerosol phases. The results are useful in understanding the dynamics of ground cloud development, atmospheric dispersion, and potential environmental effects of Shuttle effluents.

Cofer, W. R., III↗