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All sourcesNASA NTRSDOE OSTI
NASA NTRS1975

Water and soil biotic relations in Mercury distribution

The distribution of Hg is considered both in terms of its availability in soil fractions and the relationship between Hg in plant samples and Hg in ambient soils or other supportive media. The plants were grouped by habitat into epipedic-epiphytic (mosses, lichens) and endopedic-aquatic-marine (Basidiomycetes and algae) samples; nonvascular and vascular forms were also distinguished. Sources included Alaska, Hawaii, New England and Iceland. Brief consideration was also given to Hg distribution in a plant-animal-soil community. Data were expressed in terms of plant Hg content and plant substratum concentration ratio. Average Hg contents and concentration ratios, and modal ranges for the ratios were determined. The results showed similar average Hg contents in all groups (126 to 199 ppb) but a low value (84 ppb) in the lichens; terrestrial forms had ratios of 3.5 to 7.6 whereas the marine algae yielded a figure of 78.7. A secondary mode in the range 0 to 0.1 appeared only in the Alaska-New England Group, over 500 km distant from active thermal sites. Evidence for both exclusion and concentration behavior was obtained.

Siegel, S. M.↗
NASA NTRS1978

Summary of airborne chlorine and hydrogen chloride gas measurements for August 20 and September 5, 1977 Voyager launches at Air Force Eastern Test Range, Florida

Airborne chlorine and hydrogen chloride measurements were made in the tropospheric ground cloud following the Voyager launches of August 20 and September 5, 1977. The maximum observed hydrogen chloride concentration for both launches was about 25 to 30 parts per million (ppm) occurring typically 2 to 6 minutes after launch. By completion of the sampling mission (1-1/2 hours for August, 4-1/2 hours for September), the maximum in-cloud concentration decayed to about 1 to 2 ppm. Maximum observed chlorine concentrations were about 40 to 55 parts per billion (ppb) about 2 to 8 minutes after launch; by about 15 minutes after launch, chlorine concentrations were less than 10 ppb (detection limit). In-cloud chlorine concentrations were well below 1 percent of hydrogen chloride concentrations. The appendix of the report discusses the chlorine instrument and the laboratory evaluation of the detector.

Gregory, G. L.↗
NASA NTRS1978

Application of ion chromatography to the study of hydrolysis of some halogenated hydrocarbons at ambient temperatures

The application of ion chromatography to the study of very slow rates of hydrolysis of some halogenated hydrocarbons was investigated. The halide concentrations in the aqueous phase of mixtures of a carbonate buffer (pH = 10.3) and either chloroform (CHC13) or fluorotrichloromethane (CFC13) after aging for various lengths of time at room temperature, were determined by ion chromatography. Hydrolysis of CHC13 caused the C1(-) concentration to increase by about 1500 ppb per day. On the other hand neither the F(-) or C1(-) concentration in the CFC13 mixture increased by as much as 1 ppb per day. The magnitude of errors in the determination of halides prevented any firm conclusions regarding hydrolysis in this mixture. However, these results were used to show how ion chromatography could expedite identification of the hydrolyzing substance as well as investigations of hydrolysis mechanisms.

Otterson, D. A.↗
NASA NTRS1979

Launch vehicle effluent measurements during the May 12, 1977, Titan 3 launch at Air Force Eastern Test Range

Airborne effluent measurements and cloud physical behavior for the May 21, 1977, Titan 3 launch from the Air Force Eastern Test Range, Fla. are presented. The monitoring program included airborne effluent measurements in situ in the launch cloud, visible and infrared photography of cloud growth and physical behavior, and limited surface collection of rain samples. Airborne effluent measurements included concentrations of HCl, NO, NOx, and aerosols as a function of time in the exhaust cloud. For the first time in situ particulate mass concentration and aerosol number density were measured as a function of time and size in the size range of 0.05 to 25 micro meters diameter. Measurement results were similar to those of earlier launch monitorings. Maximum HCl and NOx concentrations ranged from 10 ppm and 500 ppb, respectively, several minutes after launch to about 1 ppm and 100 ppb at 45 minutes after launch.

Gregory, G. L.↗
NASA NTRS1979

Launch vehicle effluent measurements during the August 20, 1977, Titan 3 launch at Air Force Eastern Test Range

Airborne effluent measurements within the launch cloud and visible and infrared measurements of cloud physical behavior are discussed. Airborne effluent measurements include concentrations of HCl, Cl2, NO, NOX, and particulates as a function of time during each sampling pass through the exhaust cloud. The particle size distribution was measured for each pass through the cloud. Mass concentration as a function of particle diameter was measured over the size range of 0.05- to 25 micron diameter, and particle number density was measured as a function of diameter over a size range of 0.5 to 7.5 micron. Effluent concentrations in the cloud ranged from about 30 ppm several minutes after launch to about 1 to 2 ppm at 100 minutes. Maximum Cl2 concentrations were about 40 to 55 ppb and by 20 minutes were less than 1.0 ppb. A tabulated listing of the airborne data is given in the appendix. Usable cloud imaging data were limited to the first 16 minutes after launch.

Woods, D. C.↗
NASA NTRS1978

DACOM - A rapid, high sensitivity airborne carbon monoxide monitor

A rapid, high sensitivity differential absorption carbon monoxide monitor (DACOM) has been developed to measure CO from an aircraft. The differential absorption measurement is accomplished by rapidly current tuning the wavelength of a PbSSe diode laser across a single 4.7 micron CO absorption line. As the laser wavelength sweeps periodically across the absorption line, the laser beam is amplitude modulated and is then synchronously detected. With this technique a minimum detectable differential transmission of 0.02% is obtained for a 1 second integration time. This performance is equivalent to a CO sensitivity of 5 ppb for a 10 meter absorption path. The techniques used to achieve this high sensitivity will be discussed. In the aircraft installation a 10 meter absorption path is located in the airstream along the fuselage of a C-54 aircraft. During flight tests of DACOM, a sensitivity of 20 ppb for a 1-second integration time has been achieved.

Sachse, G. W.↗
NASA NTRS1979

Li, Be, and B in minerals of a refractory-rich Allende inclusion

The abundances of Li, Be, and B and the isotopic ratios of Li and B have been measured by ion microprobe in melilite, pyroxene, anorthite, and spinel grains in a coarse-grained inclusion from the Allende meteorite. Based on the measurements, it is estimated that the bulk inclusion contains 200 ppb Li, 310 ppb Be, and 18 ppm B. The B is probably due to contamination. The Li-7/Li-6 ratios in spinels, pyroxene, and melilite are indistinguishable at the + or - 15% level and lie within the uncertainty (+ or - 15%) of the range of values reported for samples of the earth and meteorites. It has been determined that this inclusion contains an excess of Al-correlated Mg-26, implying that Al-26 was once present in it. The Li-Be-B effects for two solar-system proton-irradiation models which propose to account for Al-26 in Allende inclusions have been calculated. It is found that the predicted Li-Be-B abundances and isotopic ratios are grossly different from those observed in any solar-system materials.

Phinney, D.↗
NASA NTRS1980

Remote infrared heterodyne radiometer measurements of atmospheric ammonia profiles

An infrared heterodyne radiometer has been used to study the seasonal variation of the vertical distribution of atmospheric ammonia. The ammonia profiles are inferred from high-resolution atmospheric solar transmittance measurements around the ammonia absorption feature at 927.32323 kaysers. The transmittance data are obtained from six IF channels with spectral resolutions ranging from .0067 to .033 kaysers. Results from this study show a marked decrease in the tropospheric ammonia level with a decrease at ground level from approximately 10 ppb in March 1979 to 1.3 ppb in August 1979.

Hoell, J. M.↗
NASA NTRS1980

The vertical distribution of tropospheric ammonia

A one-dimensional tropospheric photochemical model is used to simulate measured profiles of NH3 obtained with the Infrared Heterodyne Radiometer. The relative roles of homogeneous loss, heterogeneous loss, and vertical eddy transport are discussed in terms of selecting parameters which best fit the measurements. The best fit was obtained for a vertical eddy diffusion coefficient of 200,000/sq cm per sec or greater (corresponding to a characteristic vertical transport time in excess of about 35 days), and a characteristic heterogeneous loss time in excess of 10 days. The characteristic homogeneous chemical loss time was found to be about 40 days at the surface and decreased to about 180 days at 10 km, and not very sensitive to model chemical perturbations. Increased ground-level concentrations of NH3 to about 10 ppb, compared to background surface concentrations of about 1 ppb, were measured several weeks after application of ammonium nitrate fertilizer. This suggests that the volatilization of ammonium nitrate fertilizer is rapid, and an important source of NH3. Because of the characteristic times for the loss mechanisms, synoptic time-scale phenomena may play an important role in determining the tropospheric distribution of NH3 concentrations.

Levine, J. S.↗
NASA NTRS1984

Ge abundances in the lunar mantle and implications for the origin of the Moon

Regardless of the origin of the Moon, metal segregation must have occurred within the moon in order to account for its low siderophile element abundances relative to the Earth or chondrites. Germanium is a strongly siderophile element whose bulk distribution coefficient indicates that it is not fractionated during igneous processes on the Moon. The variability in absolute Ge abundances in mare basalts and pristine highland rocks, rather than elemental ratios, can be used to infer lunar mantle abundances and processes. Literature data have been compiled for Ge abundances in mare basalts and pristine highland rocks. For some landing sites, samples with 12 ppb Ge were considered to be extreme outliers and are not included. The Apollo 15 samples are enriched in Ge by a factor of 2.5 over the Apollo 12, 16 and 17 samples. Other siderophile element variations have been found in the Moon. Based on this data, best estimate of the average Ge abundance in the silicate portion of the Moon is 3.52 ppb. The Moon is depleted, relative to chondritic abundances, by a factor of 38,000 normalized to Si. Two possible explanations for the observed variations in Ge abundance in the Moon are: (1) more metal may have segregated from some regions of the Moon than from others; or Ge-bearing material may been been added later in the evolution of the Moon.

Dickinson, T.↗
NASA NTRS1984

Sulfur dioxide and particles in quiescent volcanic plumes from Poas, Arenal, and Colima volcanos, Costa Rica and Mexico

Measurements of SO2 emission rates and concentrations and of particle distribution, size, shape, and composition were made in quiescent volcanic plumes emitted into the troposphere from Poas and Arenal volcanos, Costa Rica, and Colima volcano, Mexico. SO2 emission rates were 700 + or - 180 metric tons per day (t/d) for Poas, 210 + or - 30 t/d for Arenal, and 320 + or - 50 t/d for Colima. The concentrations of SO2 calculated from the COSPEC/lidar data were 5-380 ppb. Concentrations of SO2 measured directly by flame photometry were 10-250 ppb. Particles collected in the plumes with a quartz crystal microbalance impactor were mostly less than 3 microns in diameter and consisted of droplets of dilute sulfur-bearing solutions and minor amounts of layer silicate particles coated with a sulfur-bearing film or crust. Total particle concentrations were 4.7 micrograms per cu.m for Poas and 18.8 micrograms per cu.m for Colima. Comparison of concentrations of SO2 in the plumes with gas samples collected at fumaroles on the ground suggests that the plumes are diluted by the atmosphere by factors of up to 100,000.

Casadevall, T. J.↗
NASA NTRS1986

Seasonal variations of troposheric ozone at Natal, Brazil

An analysis of ozone measurements from Natal, Brazil (6 deg S, 35 W), with a focus on the seasonal behavior in the troposphere, is presented. The amplitude of seasonal cycle at Natal is much larger than at Panama (9 deg N), the only other tropical site for which similar data are available. Concentrations of ozone in the middle troposphere in the southern spring are unexpectedly high, 60-70 ppb, similar to values found at northern midlatitudes in summer, and larger by 20-30 ppb than values found at Panama and at southern midlatitudes. It is suggested that photochemical production of ozone associated with emissions of CO, hydrocarbons, and NO(x) from biomass burning may contribute significantly to the high values of ozone, but note that stratospheric intrusions could also play a role. The data available at present do not permit a definitive evaluation of the relative importance of these two sources of ozone. The data from Natal, in combination with recent aircraft and surface data, show that tropical ozone exhibits strong spatial and temporal inhomogeneities. The distribution of tropospheric ozone appears to be considerably more complex than the traditional view, which suggested a northern midlatitude maximum and north/-south hemispheric asymmetry. The seasonal cycle in the total column of ozone at Natal appears to mirror the behavior of the tropospheric contribution to the ozone column rather than the stratospheric contribution, and this may account for differences in the annual cycle of the total column at Natal versus other tropical locations.

Logan, J. A.↗
NASA NTRS1987

Northwest Airlines flight experiments

An experiment was conducted in which real-time Total Ozone Mapping Spectrometer (TOMS) data was compared with Northwest Airlines upper air charts. It was demonstrated that the regions of steep gradient in total ozone corresponded with fronts in the upper troposphere, specifically breaks in the tropopause associated with jet streams. Other small scale structures in the ozone could be related to minor trough and ridge lines. This suggests that the relation between total ozone and tropopause height might apply even on relatively small scales, and an analysis produced high correlation coefficients provided that the air mass origin was considered. In a second test, cabin ozone mixing at 37,000 ft. varied from less than 100 ppb (300 DU total ozone) to greater than 300 ppb in a trough (400 DU total ozone). A third analysis showed that clear air turbulence was located where upper air fronts were in rapid motion as suggested by comparison of the 1200 UT synoptic charts and the ozone map taken about six hours later.

Krueger, Arlin J.↗
NASA NTRS1987

Atmospheric infrared emission of ClONO2 observed by a balloon-borne Fourier spectrometer

ClONO2 was observed in high-resolution infrared emission spectra obtained on Nov. 6, 1984, by a balloon-borne Fourier spectrometer. The observations took place near 0300 LT at a latitude of 35 N. Spectral simulations are used to determine the mixing ratios of ClONO2. This analysis incorporates line by line calculations and new ClONO2 cross sections measured in the laboratory at 223 K. The inferred mixing ratios of ClONO2 are 1.3 + or - 0.45 ppb and 0.98 + or - 0.35 ppb at 14 and 34 mbar. One-dimensional photochemical model predictions are compared to the observations. The ClONO2 mixing ratio at 34 mbar appears to be larger than theory, while there is agreement at 14 mbar.

Massie, S. T.↗
NASA NTRS1988

Photochemistry of biogenic emissions over the Amazon forest

The boundary layer chemistry over the Amazon forest during the dry season is simulated with a photochemical model. Results are in good agreement with measurements of isoprene, NO, ozone, and organic acids. Photochemical reactions of biogenic isoprene and NOx can supply most of the ozone observed in the boundary layer. Production of ozone is very sensitive to the availability of NOx, but is insensitive to the isoprene source strength. High concentrations of total odd nitrogen (NOy) are predicted for the planetary boundary layer, about 1 ppb in the mixed layer and 0.75 ppb in the convective cloud layer. Most of the odd nitrogen is present as PAN-type species, which are removed by dry deposition to the forest. The observed daytime variations of isoprene are explained by a strong dependence of the isoprene emission flux on sun angle. Nighttime losses of isoprene exceed rates of reaction with NO3 and O3 and appear to reflect dry-deposition processes. The 24-hour averaged isoprene emission flux is calculated to be 38 mg/sq m per day. Photooxidation of isoprene could account for a large fraction of the CO enrichment observed in the boundary layer under unpolluted conditions and could constitute an important atmospheric source of formic acid, methacrylic acid, and pyruvic acid.

Jacob, Daniel J.↗
NASA NTRS1988

Iridium abundance maxima in the Upper Cenomanian extinction interval

Two iridium abundance peaks, both 0.11 ppb (whole-rock basis) over a local background of 0.017 ppb, have been found in Middle Cretaceous marine rocks near Pueblo, Colorado. They occur just below the 92-million-year-old Cenomanian-Turonian (C-T) stage boundary. No other peaks were found in 45 meters of strata (about 2.5 million years of deposition) above and below the boundary interval. The broad lower peak straddles the first in a series of extinctions of benthic and nektonic macrobiota which comprise the C-T extinction event. The sharp upper peak occurs stratigraphically about 1.2 meters above the lower peak. The excess Ir might be from meteoroid impacts.

Orth, C. J.↗
NASA NTRS1988

Sulfur dioxide at the Venus cloud tops, 1978-1986

Ultraviolet spectroscopy from the Pioneer Venus Orbiter shows a decline in the cloud top abundance of SO2 from about 100 ppb to about 10 ppb in the period 1978-1986. A consistent decline in polar haze has occurred over the same period, with the correlation coefficient between these two observables of r = 0.8. Star calibrations determine the instrument sensitivity to within 10 percent which rules out the possibility that this is an instrumental effect. Systematic errors could increase the SO2 abundance to twice the inferred values in later orbits. Tracking of SO2 features and power spectral analysis give rotation periods for the longer-lived features of 3.6-5.2 days, consistent with cloud-tracked winds observed at other wavelengths. The behavior of SO2 and polar haze can be plausibly explained by episodic injection of SO2 into the cloud top regions, for example, by active volcanism.

Esposito, Larry W.↗
NASA NTRS1988

Volatile/mobile trace elements in meteoritic, non-lunar basalts: Guides to Martian sample contents

A variety of genetic processes on or in extraterrestrial objects can be examined by study of volatile/mobile trace elements. Doubtless, considerable efforts will be expended on determining these elements in returned Martian samples. The purpose is to estimate levels of such elements expected to be present in returned Martian samples. Some ideas about Martian genesis were already advanced from the volatile/mobile element contents in SNC meteorites, assuming that Mars was their parent body. Even is Mars and the SNC meteorite parent body are identical, compositional ranges for returned Martian samples should exceed those of SNC meteorites. It is expected, therefore, that Martian samples returned from locations other than Polar regions will have indigenous volatile/mobile element contents within howardite-diogenite ranges. Elements with strong lithophile tendences may be more abundant, as they are in many lunar samples. Most of these elements should be at ppb levels except for Co, Ga, Zn, and Rb, which should lie at ppm levels. If Martian volcanism was accompanied by fumarolic emanations, it should be reflected in occasional huge enrichments of mobile trance elements, as in lunar meteorite Y 791197. During collection and transport Earthward, samples must be contained under conditions appropriate to ppb concentrations. Materials must be used that will not cause contamination which occurred during the Apollo program, where indium from seals contaminated many samples.

Lipschutz, M. E.↗