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Breig, E. L.

Publications and source records attributed to Breig, E. L..

At least 19 records

Charge transfer and momentum exchange in exospheric D-H(+) and H-D(+) collisions

Mechanisms that control the escape of deuterium from planetary exospheres include the acceleration of D(+) in the polar wind, and the production of suprathermal D atoms through nonthermal collisions. In this paper we examine the effects of neutral-ion interactions involving deuterium and hydrogen on the velocity distribution of neutral D. A two-center scattering approximation is used as the basis for calculations of the differential cross sections for charge transfer and elastic scatter in collision of H with D(+) and of D with H(+) for ionosphere-exosphere collision energies below 10 e V. These data are used to derive temperature dependent rate coefficients for the charge transfer branches of these interactions, and to determine the effects of ion-neutral temperature differences on the rate of generation of suprathermal D through charge transfer and elastic scatter.

Hodges, R. R., Jr.↗

Deuterium and hydrogen flows in the thermosphere

Processes that affect vertical distributions and flows of deuterium and hydrogen between 100 and 500 km in the daytime thermosphere are investigated using a steady state numerical model that includes HD and H2 molecular flows, relevant chemistry, and transport by both molecular and eddy diffusion. The results of calculations indicate that the outward thermospheric fuxes and, hence, the planetary loss rates for D must be large compared to evaporative escape (as is also the case for H), confirming the suggestion of Breig et al. (1987). Results of measurements of H in the mesosphere and lower thermosphere and of H and D in the thermosphere were used to derive upward fluxes through the daytime thermosphere, showing that the upward fluxes exceeded the corresponding Jeans evaporative escape rates by factors of about 5 for H, and greater than 500 for D.

Breig, E. L.↗

Ionosphere-exosphere coupling through charge exchange and momentum transfer in hydrogen-proton collisions

The implications of a traditional assumption of exospheric physics, that collisions of hydrogen atoms and protons preferentially result in charge exchange with negligible momentum transfer are examined. Initially adopted as a necessary convenience to accommodate limited computer resources in exosphere model calculations, this approximation results in a direct transformation of the proton velocity distribution into a hot component of neutral hydrogen. With expanding computational facilities, the need for the approximation has passed. As the first step toward its replacement with a realistic, quantum mechanical model of the H - H(+) collision process, differential and cumulative cross sections were calculated for quantum elastic scattering of indistinguishable nuclei for a fine grid of encounter energies and scattering angles. These data are used to study the nature of ionosphere-exosphere coupling through H - H(+) collisions, and to demonstrate that the distribution of velocities of scattered H produced in the traditional exospheric charge exchange approximation, as well as that arising from an alternative, fluid dynamic approach, leads to unacceptable abundances of coronal atoms in long-term, highly elliptic trajectories.

Hodges, R. R., Jr.↗

Latitudinal variation of thermospheric hydrogen near solstice from AE-D observations

Variations of thermospheric neutral atomic hydrogen with latitude during a solstice season near solar minimum were investigated using data acquired with the polar-orbiting AE-D satellite. Hydrogen concentrations at low latitude were found to be comparable to those found from observations with the AE-E satellite, but were slightly higher than concentrations derived from the 1983 mass spectrometer incoherent scatter atmospheric model. Results confirm the general summer-to-winter density increase, large latitudinal gradients in the summer hemisphere, and the winter enhancement of hydrogen observed in AE-C nighttime measurements. The AE-D data, however, show a small polar depression in hydrogen concentration at high winter latitudes, attributed to atmospheric dynamics following auroral heating. The density gradients observed by AE-D in the summer hemisphere were in sharp contrast to the more constant horizontal daytime profiles reported from OGO-6 and previous AE-C measurements, indicating the possibility of local time effects.

Sanatani, S.↗

Thermospheric ion and neutral composition and chemistry

A summary is presented of research contributions by U.S. scientists during the years 1983-1986, toward an increased understanding of the properties and behavior of the earth's thermosphere and F-region ionosphere. As part of the more extensive aeronomy report to IUGG, this review addresses specifically the composition and relevant chemical and thermal processes that influence this region of the atmosphere. The discussion focuses on the separate neutral and ion species, and on the temperatures of the electrons, ions, and neutral gas. Related aspects of the solar radiation and photoelectrons are also included. Direct observational results and analyses are emphasized, along with references to pertinent findings from basic laboratory and theoretical studies.

Breig, E. L.↗

Deuterium in the daytime thermosphere

Ion concentration measurements for H(+) and D(+) from the magnetic ion mass spectrometer on the Atmosphere Explorer C satellite are used, in conjunction with other atmospheric data, to determine the concentrations of H and D in the nonpolar daytime thermosphere. The ratio of the observed D(+) to H(+) concentrations has essentially the same height dependence in the 300 to 800-km region as expected for their neutral counterparts, even in the presence of ion temperature gradients and probable large vertical ion fluxes. Rapid charge exchange with atomic oxygen ensures that D/H is about equal to D(+)/H(+) at the lower altitudes where the derived D to H concentration ratio is a factor of about 6 larger than its sea level value, for an exospheric temperature of 930 K. This relative enhancement of deuterium arises from the fact that hydrogen more readily escapes the earth, and a large vertical gradient in the H concentration relative to its diffusive equilibrium value is necessary to drive this upward flux through the lower thermosphere. If these planetary losses of hydrogen are much greater than those associated with evaporative escape, as is the current view, then correspondingly larger deuterium loss rates are also likely in order that the thermospheric D/H ratio not increase well above the observed value. The absolute winter daytime concentration of deuterium at 300 km is found to be 210 + or - 50 atoms/cu cm.

Breig, E. L.↗

Thermospheric hydrogen - The long-term solar influence

Atmospheric Explorer C and E satellite data are employed for a long-term analysis of the behavior of thermospheric hydrogen with respect to the 11 yr solar cycle. The data covered the period 1974-79 (increasing solar activity) and comprised in situ ionospheric (F region) and neutral atmospheric data. The data were analyzed statistically to characterize low latitude hydrogen behavior, e.g., the diurnal variation and mean concentration over the 5 yr data sampling period. Both the mean and daily maximum/minimum ratio (DMMR) varied with the solar F index. The escaping flux of H ions became a contant around 1000 K. Increasing thermospheric temperatures lowered the DMMR value. However, the DMMR values calculated were consistently large enough to require inclusion of neutral winds and/or diurnal variations in charge exchange fluxes moving in and out of the plasmasphere in any model for thermospheric hydrogen behavior.

Breig, E. L.↗

Results of a comprehensive study of the photochemistry of N2(+) in the ionosphere

The improved match that can be obtained between the Atmospheric Explorer (AE) data on the ionospheric F layer N2(+) abundance and theoretical predictions by changing the dissociative recombination rate coefficient is demonstrated. Historically, models have overestimated the N2(+) concentration. It is shown that the calculated enhancement is due to charge exchange between 0(+)(2D) with N2. Increasing alpha by a factor of 2-3, at least in the orbits examined, can augment the destruction of vibrationally excited N2(+) ions. However, the validity of the correction is dependent on the availability of further laboratory data.

Abdou, W. A.↗

Relative abundance of the light ions in the winter nighttime topside ionosphere

Ion concentration measurements with the retarding potential analyzer onboard OGO 6 satellite have served as basis for investigation of the distribution of the light ions, H(+) and He(+), relative to that of O(+) in the 500- to 800-km height range in the winter nighttime ionosphere. This concentration ratio exhibits distinct large-scale horizontal variations, with a relative depression in the ratio observed over a broad region about -45 deg longitude northward of approximately 40 deg dip latitude. The lower ratios are associated primarily with well-defined relative increases in the abundance of O(+), and occur in the same longitude sector that has been characterized in an earlier study by both an observed concurrent relative enhancement in ion temperature and the presence of large fluxes of energetic electrons. Comparisons are presented for the altitude distributions of the concentration ratio between regions representing extremes of the horizontal variation. A simple diffusive-equilibrium model demonstrates that the effects of ion temperature on the O(+) vertical distribution are a significant factor leading to the observed variation of the concentration ratio.

Sanatani, S.↗

Ionospheric chemistry of NO(+)

An investigation is described of the behavior of NO(+) in the daytime F region, with basic ion concentration measurements from the Atmosphere Explorer C satellite. The data set was acquired along select orbits at low latitudes and exhibits substantial variations in the NO(+) concentration, both along and between nearby orbits. An excellent consistency is demonstrated between these observations and current chemical equilibrium theory, in contrast to differences that have been reported for the related N2(+) ion. Large variations in the concurrently observed electron temperature permit a relevant comparison between different laboratory determinations of the dissociative recombination rate coefficient. Contributions to the NO(+) production from several secondary sources are also evaluated. Results strengthen the basis for the current theoretical ionospheric chemistry of NO(+) and establish important constraints on resolution of the difficulties with N2(+).

Breig, E. L.↗

Photochemistry of N2(+) in the daytime F region

The photochemistry of N2(+) in the daytime F region continues to be a source of concern due primarily to the uncertain roles of the metastable O+(2D) ion and possible vibrational excitation. This investigation adopts a unique subset of data from the Atmospheric Explorer C satellite that spans distinct regions near the low-latitude F peak wherein either chemical reactions or electron processes alternatively control the N2(+) abundances. Concentrations of N2(+) calculated according to current theory and including recent laboratory data for O+(2D) losses via N2 are found to exceed ionospheric observations between 220 and 400 km by a factor near 2. Relevant characteristics of the basic molecular ion concentration measurements are described, along with an analysis for select orbits conducted according to current photochemical equilibrium theory. Possible simple modifications of this theory are discussed in terms of the constraints suggested by the nature of the observations.

Breig, E. L.↗

Observations and photochemistry of O/++/ in the daytime thermosphere

An analysis is conducted for the Atmosphere Explorer C observations of O(++) in the daytime thermosphere which supercedes that of Breig et al (1977) and restricts attention to five orbits of data from the high-grain mode of the magnetic ion-mass spectrometer. The present investigation adopts a model for O(++) ionospheric chemistry which has been revised in light of recent laboratory measurements of a fast loss rate for O(++) through reaction with N2. An improved procedure is also introduced which analyzes the basic ion currents recorded by the magnetic ion-mass spectrometer and has special application for the very low concentrations near and below 200 km. It is found that large scale features in the low altitude data are best represented with an additive term which is proportional to the N2 or O2 density, with the preferred interpretation as a contaminant signal induced by neutral particles impinging on instrument or spacecraft surfaces.

Breig, E. L.↗

Winter nighttime ion temperatures and energetic electrons from OGO 6 plasma measurements

In the reported investigation, ion temperature and suprathermal electron flux data were acquired with the retarding potential analyzer on board the OGO 6 satellite when it was in solar eclipse. Attention is given to measurements in the 400- to 800-km height interval between midnight and predawn in the northern winter nonpolar ionosphere. Statistical analysis of data recorded during a 1 month time span permits a decoupling of horizontal and altitude effects. A distinct longitudinal variation is observed for ion temperature above 500 km, with a significant relative enhancement over the western North Atlantic. Altitude distributions of ion temperature are compatible with Millstone Hill profiles within the common region of this enhancement. Large fluxes of energetic electrons are observed and extend to much lower geomagnetic latitudes in the same longitude sector.

Sanatani, S.↗

Neutral thermospheric temperature from ion concentration measurements

A technique for extracting information on neutral temperature from in situ F region measurements of O(+) and H(+) ion concentrations is analyzed and evaluated. Advantage is taken of the condition of charge-exchange equilibrium of these species in the neighborhood of 320 km to infer the associated relative abundances of neutral oxygen and hydrogen. Results are shown to be generally consistent with other concurrent in situ measurements.

Breig, E. L.↗

Nighttime temperatures and ion chemistry from OGO 6 plasma measurements

Results are presented of a statical investigation of temperature and molecular ion chemistry in the nighttime thermosphere, with data from plasma measurements between 400 and 450 km from the retarding potential analyzer on the OGO 6 satellite. Temperatures and ion concentrations from the equatorial region are discussed. Emphasis is placed on statistical analyses of all data acquired within small cells of finite width in latitude and day of observation. Attention is given to a significant fraction of the nighttime hemisphere between low summer and middle winter latitudes.

Sanatani, S.↗

Direct in situ measurements of thermospheric temperature

The open source neutral mass spectrometer on the Atmosphere Explorer satellites used for direct in situ measurements of the neutral gas temperature by means of the 'fly-through' mode of operation is evaluated. The derived neutral temperature (Tn) is compared with ion temperatures (T1) obtained simultaneously from the on-board retarding potential analyzer for altitudes and conditions where the two temperatures should be equal. A statistical analysis showed consistency between concurrently observed values of Tn and T1, also shown through profiles depicting their altitude distributions between 150 and 225 km. The overall magnitude of temperatures calculated from the Jacchia (1971) model results in a better representation of the observations than the higher temperatures predicted for this region by the MSIS model (Hedin, 1977), and agreement is also found between observed temperatures and neutral temperatures derived from altitude distributions of N2 particle densities.

Kayser, D. C.↗

Doubly charged atomic oxygen ions in the thermosphere. I - Photochemistry

Measurements of O(++) concentrations made by the Atmosphere Explorer C satellite are analyzed for altitudes where photochemical equilibrium conditions prevail in order to determine the photochemical sources and sinks of the doubly charged ion. The major loss process is found to be through partial charge exchange with neutral atomic oxygen with a rate coefficient of 1 x 10 to the -11th cu cm/s with an uncertainty of 40%. Above 220 km the major source is photo-ionization of O(+). However, X ray ionization of O (at not greater than 23.3 A) producing O(++) directly through the Auger process provides a better fit to the observed profile at lower altitudes.

Breig, E. L.↗