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  • 1
    Publication Date: 2006-02-14
    Description: Recent atmospheric calculation suggest that the prebiological atmosphere was most probably composed of nitrogen, carbon dioxide, and water vapor, resulting from volatile outgassing, as opposed to the older view of a strongly reducing early atmosphere composed of methane, ammonia, and hydrogen. Photochemical calculations indicate that methane would have been readily destroyed via reaction with the hydroxyl radical produced from water vapor and that ammonia would have been readily lost via photolysis and rainout. The rapid loss of methane and ammonia, coupled with the absence of a significant source of these gases, suggest that atmospheric methane and ammonia were very short lived, if they were present at all. An early atmosphere of N2, CO2, and H2O is stable and leads to the chemical production of a number of atmospheric species of biological significance, including oxygen, ozone, carbon monoxide, formaldehyde, and hydrogen cyanide. Using a photochemical model of the early atmosphere, the chemical productionof these species over a wide range of atmospheric parameters were investigated. These calculations indicate that early atmospheric levels of O3 were significantly below the levels needed to provide UV shielding. The fate of volcanically emitted sulfur species, e.g., sulfur dioxide and hydrogen sulfide, was investigated in the early atmosphere to assess their UV shielding properties. The photochemical calculations show that these species were of insufficient levels, due in part to their short photochemical lifetimes, to provide UV shielding.
    Keywords: GEOPHYSICS
    Type: NASA, Washington Second Symposium on Chemical Evolution and the Origin and Evolution of Life; p 47
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  • 2
    Publication Date: 2011-08-19
    Description: Seasonal and diurnal emissions of NO and N2O from agricultural sites in Jamestown, Virginia and Boulder, Colorado are estimated in terms of soil temperature; percent moisture; and exchangeable nitrate, nitrite, and ammonium concentrations. The techniques and procedures used to analyze the soil parameters are described. The spatial and temporal variability of the NO and N2O emissions is studied. A correlation between NO fluxes in the Virginia sample and nitrate concentration, temperature, and percent moisture is detected, and NO fluxes for the Colorado site correspond with temperature and moisture. It is observed that the N2O emissions are only present when percent moisture approaches or exceeds the field capacity of the soil. The data suggest that NO is produced primarily by nitrification in aerobic soils, and N2O is formed by denitrification in anaerobic soils.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 92; 965-976
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  • 3
    Publication Date: 2011-08-19
    Description: Daytime and nighttime vertical profiles of the tropospheric trace gas N2O were determined from grab sample collections off the Atlantic and Gulf coasts of Florida. The grab samples were collected during the week of October 7-13, 1984, from a Lear jet during descent spirals over an altitude range of 12.5-0.3 km in approximately 1.2-km intervals. During this period there were two distinct airflow regimes sampled: (1) the surface boundary layer (less than 2 km), in which the wind direction was typically easterly; and (2) the regime above the boundary layer, which was predominantly characterized by westerly flow. N2O mixing ratios, normalized to dry air, were determined from 148 daytime and nighttime samplings. N2O was found to be uniformly mixed at all altitudes at 301.9 + or - 2.4 parts per billion by volume.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 91; 11911-11
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  • 4
    Publication Date: 2011-08-19
    Description: Smoke-plume gas samples were collected at altitudes from 35-670 m above the ground over the San Dimas Experimental Forest during a 400-acre prescribed chaparral fire. Mean emission ratios relative to CO2 for CO, H2, CH4, and total nonmethane hydrocarbons were lower than previous values obtained for large biomass-burning field experiments. Comparison of samples from vigorously flaming and mixed stages of combustion revealed little differences in CO2 normalized emission ratios for these gases (except for N2O).
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 93; 1653-165
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  • 5
    Publication Date: 2011-08-19
    Description: The vertical distributions of molecular hydrogen (H2) and carbon monoxide (CO) were determined during spiraling maneuvers from aircraft off the eastern coast of the United States and over the Gulf of Mexico. H2 was always at its lowest levels in the boundary layer, averaging about 500 parts per billion by volume (ppbv). H2 mixing ratios determined in the free troposphere were typically higher (600-700 ppbv), and often suggested a small progressive increase with altitude. Several large free-tropospheric H2 plumes (mixing ratios as high as 1-2 parts per million by volume) were implied by the data. These H2 plumes were not always accompanied by corresponding increases in CO mixing ratios. This result is most difficult to explain when it is noted that the primary atmospheric sources for molecular H2 are considered to be combustion and photochemistry, both of which should be strong CO sources also.
    Keywords: GEOPHYSICS
    Type: Journal of Geophysical Research (ISSN 0148-0227); 91; 14561-14
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  • 6
    Publication Date: 2011-08-19
    Description: C2H6 absorption features in the 2980/cm spectral region of the solar spectrum recorded in April, 1951 were analyzed to determine the total vertical column amount and average free tropospheric mixing ratio of C2H6 above Jungfraujoch in the Swiss Alps. The PQ1 subbranch is the best isolated of the three C2H6 features in the 1951 spectrum, with an equivalent width of 0.0099 + or - 0.0025/cm. Results give a total vertical column amount of 9.7 x 10 to the 15th C2H6 molecules/sq cm, with an accuracy of + or - 30 percent. March 1981 measurements from this region give a mixing ratio of about 2.0 ppbv, 2.2 times larger than the 1951 value, suggesting a long-term increase in the free tropospheric C2H6 concentration over western Europe.
    Keywords: GEOPHYSICS
    Type: Applied Optics (ISSN 0003-6935); 25; 4522-452
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  • 7
    Publication Date: 2011-08-19
    Description: The first simultaneous measurements of ammonia and nitric acid in the troposphere have been made from an aircraft using a tungsten oxide denuder system. Vertical profiles of NH3 and HNO3 taken over coastal Virginia and Maryland in March and September, 1983, at altitudes from 150 m to 3000 m, show mixing ratios that decrease with altitude. Ammonia profiles show substantial seasonal variation, while nitric acid profiles do not. Using the measured profiles and a one-dimensional photochemical model, lifetimes due to heterogeneous loss of one day for HNO3 and ten days for NH3 are calculated. In contrast, NH3 profiles up to 5300 m over the North Atlantic Ocean during August 1982 show mixing ratios that increase slightly with altitude. These data represent the first ammonia profiles measured over the ocean. It is suggested that the increase in NH3 with altitude is a result of an ammonia-rich continental air mass advected over the ocean, followed by the dissolution of NH3 in the marine boundary layer on water-covered sea salt particles.
    Keywords: GEOPHYSICS
    Type: Geophysical Research Letters (ISSN 0094-8276); 12; 401-404
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  • 8
    Publication Date: 2011-08-19
    Description: The distribution of gases in the prebiologial paleoatmosphere is investigated using photochemical models. A chart of the photochemical and chemical reactions and reaction rates for CH4, NH3, H2S, N2O, and CO atmospheric gases is given. Mixing ratios and surface mixing ratios for CH4, NH3, CO, and N2O are obtained using thermodynamic equilibrium calculations; an increase in CH4 and N2O is observed. The reactions, which explain the photochemistry of the gases studied, are presented. The sources of these gases and their concentration with regards to altitude are examined. Graphs of the vertical distribution of CH4, NH3, H2S, CO, O2, and N2O in prebiological paleoatmosphere are provided. The data reveals the presence of only N2, CO2, and N2O in the early atmosphere; with the evolution of life, sources of atmospheric gases increased and their influence on the photochemistry of the troposphere and stratosphere increased.
    Keywords: GEOPHYSICS
    Type: Origins of Life (ISSN 0302-1688); 15; 4, 19
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  • 9
    Publication Date: 2011-08-19
    Description: The 1-2 percent increase in tropospheric methane determined from gas chromatographic measurements since 1977 has important implications for atmospheric photochemistry and climate. To extend the measurement baseline, solar absorption spectra have been analyzed and mean troposphere CH4 mixing ratios for the years 1951 and 1981, and an average rate of CH4 increase of 1.1 + or - 0.2 percent per year is found for this period.
    Keywords: GEOPHYSICS
    Type: Nature (ISSN 0028-0836); 318; 245-249
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  • 10
    Publication Date: 2011-08-19
    Description: Published total vertical column amounts of carbon monoxide deduced from infrared solar spectra recorded during 1950-51 in the Swiss Alps have been reanalyzed based on improved spectroscopic parameters for CO and a curve of growth. From a comparison of the 1950-51 results and modern measurements, an average increase of about 2 percent per year in the free tropospheric concentration of CO above Europe is estimated for 1950-77.
    Keywords: GEOPHYSICS
    Type: Nature (ISSN 0028-0836); 318; 250-254
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