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At least 181 records · Page 10

Germane in the atmosphere of Jupiter

Germane, GeH4, is a tetrahedral molecule like methane. The nu 3 fundamental mode of GeH4 falls in the middle of the 5-micrometer Jupiter window. Jupiter observations were made in December 1975 during three flights with the 0.9-m telescope of the Kuiper Airborne Observatory. The spectrometer is a rapid-scanning Michelson interferometer having InSb detectors at each of the two outputs. The germane identification procedure is based on a comparison of the obtained Jupiter spectrum with that of laboratory germane. It appears that the detection of GeH4 in Jupiter's atmosphere with a mixing ratio of 0.6 ppb is the smallest concentration of a trace constituent yet detected in a nonterrestrial planetary atmosphere. It is pointed out that a strict interpretation of thermochemical equilibrium predictions for the spectral line forming regions of Jupiter's atmosphere does not explain the observation of GeH4.

Fink, U.↗

The moon - Composition determined by nebular processes

The Ganapathy-Anders seven-component model is used as the basis for an analysis of conditions in the early solar nebula as they pertain to the formation of the moon. Calculations incorporating improved geological data and petrological constraints are presented in terms of a model moon which meets trace element restrictions and conforms to known parameters of heat flow, density, and moment of inertia ratio, ie., 40 ppb U, and a core of 2% by weight. It is noted that a melt of the model composition approximates that of Apollo 15 green glass, together with a residuum of olivine, plus 3-4% spinel.

Morgan, J. W.↗

Launch vehicle effluent measurements during the September 5, 1977, Titan 3 launch at Air Force eastern test range

Airborne effluent measurements and cloud physical behavior data 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. Effluent measurements included concentrations of HCl, Cl2, NO, nitric oxide, and particles as a function of time in the exhaust cloud. In situ particle mass concentration and number density were measured as a function of time and size in the range of 0.05 micron m to 30 micron m diameter. Measurement results were similar to those of previous launch monitorings. Maximum HCl and nitric oxide concentrations of Cl2 were maximum about 2 minutes after launch and by 10 to 15 minutes had decayed to less than 10 ppb (detection limit). Particle measurements showed most of the particles present to be below about 3-micron m diameter. Postlaunch analyses of collected particle samples showed significant amounts of Al (some cases Cl) from about 3-micron m to 0.04-micron m diameter.

Wornom, D. E.↗

Tropospheric ozone

Photochemical equilibrium models have been used to study the effect of recent revisions in important chemical reaction rates on the calculated tropospheric ozone concentration. Reasonable agreement with observed values is obtained if the NO(x) background is approximately 0.02 to 0.03 ppb, about an order of magnitude less than used in many previous model studies, but consistent with present nitrogen budget considerations and with observations of NO2. Chemical production and loss of ozone may dominate transport terms depending on values of key chemical rate constants and of the NO(x) background. This is consistent with the structure observed in the mean annual latitudinal distribution of ozone since ozone is its own chemical precursor and regions of enhanced stratosphere-troposphere exchange are also regions of enhanced photochemical activity.

Stewart, R. W.↗

Effect of chlorofluoromethane infrared radiation on zonal atmospheric temperatures

Estimates are made of changes in the atmospheric climate due to the radiative effects of 10 ppb of chlorofluoromethanes (CFM's). The estimates are derived on the basis of a 12-layer stratospheric general circulation model with a specified change of ocean temperature. Two tropical maxima in zonal average temperature change were observed: one in the upper troposphere and one centered at the tropopause. The temperature change exceeds the surface temperature change by a factor of at least two. If the 1975 CFM emission rate were to continue indefinitely, stratospheric water-vapor concentrations would increase by up to 60% due to CFM radiative effects. This would reduce ozone concentrations by an additional 4% of the natural ozone column.

Dickinson, R. E.↗

Sensitivity of the predicted CO-OH-CH4 perturbation to tropospheric NOx concentrations

Measurements indicate that ambient NOx(NO + NO2) concentrations vary over at least an order of magnitude in the troposphere. Thus it is of interest to study atmospheric chemistry with NOx concentrations covering this range. In this paper we present steady state calculations which show that as NOx concentrations are increased from very low values, the hydroxyl radical concentration increases at first and then decreases. This change of behavior occurs at a concentration of NO2 of about 0.23 ppb in the model. Also, the response of the atmosphere to increased CO fluxes undergoes a qualitative change as a function of the concentration of NOx. At low levels of NOx concentration, an increase in CO fluxes into the atmosphere depletes the OH concentration and increases the concentrations of CH4 and H2, as reported in the literature. However, at high values of NOx concentration, increased CO fluxes give rise to an increase in the OH concentration and, consequently, a decrease in the concentrations of CH4 and H2.

Hameed, S.↗

Remote measurement of ClO in the stratosphere

ClO has been detected in the stratosphere from observations of the solar spectrum in the infrared, in a small spectral interval near 12 micrometers. The observations were made with a balloon-borne laser heterodyne radiometer, launched from Palestine, Texas on September 20. By comparing high sun spectra with a number of sequential spectra taken during sunset, an altitude profile has been calculated in the 29-38 km altitude range. The results show a peak mixing ratio in excess of one ppb above 34 km, and a rapid decrease in mixing ratio with decreasing altitude below 34 km.

Menzies, R. T.↗

Qualitative and quantitative flow visualization technique using ozone

The paper describes a new flow-visualization technique based on the absorption of ultraviolet light by ozone. Ozone is an excellent tracer, because as a gas it has the same effective physical properties as air. Ozone strongly absorbs the principal line (253.7 nm) of a mercury lamp, so that when an ozone-traced flow passes between a mercury lamp and a fluorescent screen, a sharp, shadow-like image of the ozone tracer is cast on the screen. Quantitative photometry can be carried out by replacing the screen with ultraviolet detectors that yield the path-integrated column density of ozone in the flow. High-speed quantitative point monitoring (10 Hz at 10 ppb O3) is possible with capillary probes and chemiluminescent analysis.

Dickerson, R. R.↗

Ries impact crater, southern Germany - Search for meteoritic material

Twenty-three samples covering a wide range of shock metamorphism from the Ries impact crater in southern Germany were analyzed for siderophile and volatile elements in order to determine the chemical nature of the impacting meteorite. Slight enrichments in the siderophile elements Ir and Os above the indigenous level of 0.015 ppb were observed in only eight samples, including a shocked, metal-bearing amphibolite and two weakly shocked biotite gneisses, whereas those samples expected to contain meteoritic material (heavily shocked glasses) do not exhibit a perceptible siderophile enrichment. The Ir, Os and Ni enrichments of the metal bearing amphibolite are found to be compatible with chondritic ratios, while in the other enriched samples, Ir, Ni and Se relationships suggest an achondritic meteoritic origin. An aubritic projectile is concluded to be most compatible with the data.

Morgan, J. W.↗

Further laboratory studies and stratospheric flight of a mass spectrometer beam system

A gas expansion system combined with a mass spectrometer has been tested and flown successfully in the stratosphere. Through a sequence of orifices and high speed pumping, gas particles were formed into a molecular beam and analyzed by a sensitive mass spectrometer. During two balloon flights, vertical profiles of all major atmospheric constituents as well as O3, CO2, H2O and others were obtained. Gases such as AR38 and O16;O17 provided in-flight calibration standards. The sensitivity of the system was such that gases with mixing ratios of 10 ppb at an ambient pressure of about 10 mbar were detectable.

Mauersberger, K.↗

The bounds of the heat production rate within the moon

A new approach is proposed to the evaluation of the lower and upper bounds of the global heat production rate within planetary interiors. The approach is based on the relationship between the internal energy change and the volume change of a planetary object. For illustration, the approach is applied to the moon. Using an average global surface heat flux of 18 erg/sq cm-sec, and assuming constancy of the lunar radius during the past 3.2 billion years. the lunar heat release within the past 3.2 billion years is estimated at (30 to 40) x 10 to the tenth erg/cu cm. This is equivalent to the present day uranium concentration of 35 to 50 ppb provided the radiogenic isotopes are of the same proportion as that given by Toksoz et al. (1978).

Hsui, A. T.↗

Instrument development for a toxic level hypergolic vapor detector

The development and deployment of technology applicable to the field measurement of hypergolic propellants is discussed. The propellants include hydrazine (H) monomethylhydrazine (MMH), and 1,1-dimethylhydrazine (UDMH) at the parts per billion (PPB) level in air or a diluent gas. Four major areas are reviewed: (1) development of an improved electrochemical sensor for the measurement of hydrazines (H, MMH and UDMH) in air; (2) prototype instrument fabrication and subsequent laboratory evaluation; (3) initial instrument field test results; and (4) future requirements and applications.

Rogers, P. M.↗

Ambient ammonia measurements using laser photo-acoustic spectroscopy

Ammonia concentrations reached minimal levels (approximately 0.1 ppb) in early winter, followed by a sudden later winter increase. A direct relationship between ambient ammonia levels and air temperature was inferred from the data (linear correlation coefficient r=0.53). Ammonia concentrations were determined to be directly related to the absolute humidity of the air (r=0.72); a weaker relationship between ammonia concentrations and relative humidity was discovered (r=0.37). The data also indicated that ammonia levels were generally higher within continental air masses than those of maritime origin. Soil parameters such as pH and moisture content were found to have a major bearing on the release of gaseous ammonia from soils in the region.

Aldridge, M. D., III↗

Approach to forecasting daily maximum ozone levels in St. Louis

Measurements taken in 1976 from the St. Louis Regional Air Pollution Study (RAPS) data base, conducted by EPA, were analyzed to determine an optimum set of air-quality and meteorological variables for predicting maximum ozone levels for each day in 1976. A 'leaps and bounds' regression analysis was used to identify the best subset of variables. Three particular variables, the 9 a.m. ozone level, the forecasted maximum temperature, and the 6-9 a.m. averaged wind speed, have useful forecasting utility. The trajectory history of air masses entering St. Louis was studied, and it was concluded that transport-related variables contribute to the appearance of very high ozone levels. The final empirical forecast model predicts the daily maximum ozone over 341 days with a standard deviation of 11 ppb, which approaches the estimated error.

Prior, E. J.↗

Absolute tracer dye concentration using airborne laser-induced water Raman backscatter

The use of simultaneous airborne-laser-induced dye fluorescence and water Raman backscatter to measure the absolute concentration of an ocean-dispersed tracer dye is discussed. Theoretical considerations of the calculation of dye concentration by the numerical comparison of airborne laser-induced fluorescence spectra with laboratory spectra for known dye concentrations using the 3400/cm OH-stretch water Raman scatter as a calibration signal are presented which show that minimum errors are obtained and no data concerning water mass transmission properties are required when the laser wavelength is chosen to yield a Raman signal near the dye emission band. Results of field experiments conducted with an airborne conical scan lidar over a site in New York Bight into which rhodamine dye had been injected in a study of oil spill dispersion are then indicated which resulted in a contour map of dye concentrations, with a minimum detectable dye concentration of approximately 2 ppb by weight.

Hoge, F. E.↗

Remote probing of the atmosphere using a CO2 DIAL system

An overview of our laser remote sensing effort is presented. Using both fundamental and frequency-doubled CO2 laser radiation in a differential absorption LIDAR (DIAL) system, background concentrations of CO, NO, and C2H4 in the atmosphere as well as increases due to localized emission sources have been measured. These species have been detected using the backscattered laser radiation from topographic targets at ranges to 2.7 km with a sensitivity of plus or minus 10 ppb. In addition, using a dual-laser DIAL system, the effect of induced correlation of the LIDAR returns due to atmospheric turbulence has been investigated. These results have been used to help quantify the accuracy of the DIAL measurements and are shown to be consistent with theory.

Killinger, D. K.↗

Atmospheric chemistry of ethane and ethylene

It is shown by a study of ethane and ethylene photochemistry that the loss of ethane is controlled by OH in the troposphere and Cl in the stratosphere. Ethane observations indicating free Cl concentrations below 30 km that are only 10% of the value predicted by the present model calculations cannot be explained by heterogeneous aerosol concentration processes, and contradict current stratospheric photochemistry. The chemical destruction of ethane and ethylene leads to the generation of such compounds as carbon monoxide and formaldehyde, and it is found that the tropospheric concentrations of the latter are enhanced by nearly a factor of three for an ethylene mixing ratio of 2 ppb.

Aikin, A. C.↗