Engineering topics

Solomon, S.

Publications and source records attributed to Solomon, S..

At least 37 records · Page 2

NASA NTRS1990

Interpretation of aircraft measurements of NO, ClO, and O3 in the lower stratosphere

Results are presented from an October 17, 1988, flight of the NASA ER-2 stratospheric research aircraft. The flight sampled a nearly constant air mass at 20 km altitude, near 39 deg N latitude, from before sunrise until near noon. The instrumentation on board simultaneously measured NO, ClO, O3, temperature, and pressure. The measurements are combined with modeled photodissociation coefficients and known reaction kinetics to infer abundances of other important species, and the results are compared to previous estimates as a test for consistency in the understanding of the photochemical processes governing the species distributions.

Kawa, S. R.↗

NASA NTRS1990

A diagnostic for denitrification in the winter polar stratospheres

The pairwise correlation of NO(y) and N2O data from the Southern and Northern Hemispheres is presented. Both data sets show a linear correlation region, defined as a reference state, and regions of denitrification where the correlation breaks down. Using two-dimensional photochemical model simulations of the atmosphere, a similar linear correlation is found between NO(y) and N2O, thereby establishing a theoretical framework for the reference state. This general approach, which can be extended to other pairs of molecules, should prove to be powerful in further comparisons of aircraft data with numerical models.

Fahey, D. W.↗

NASA NTRS1990

The polar stratospheric cloud event of January 24, 1989. I - Microphysics

Rapid adiabatic cooling induced by synoptic forcing led to polar stratospheric cloud (PSC) formation on January 24, 1989, at altitudes sampled by the ER-2 aircraft. Particle characteristics measured by the Forward Scattering Spectrometer Probe (FSSP) on the ER-2 were compared to those calculated using a theoretical PSC microphysics model. Although calculations were sensitive to local changes in cooling rate, generally favorable agreement was found, that in particle surface area being especially important since this parameter dictates heterogeneous chemical rates. The overall model performance suggests that the current approach for simulating Type 1 (nitric acid trihydrate) PSC formation under rapid cooling conditions is well founded and can be used to study the effects of heterogeneous chemistry on stratospheric composition.

Poole, L. R.↗

NASA NTRS1990

The polar stratospheric cloud event of January 24. II - Photochemistry

During the 1988/89 Airborne Arctic Stratospheric Expedition (AASE), observations of the chemical composition, aerosol characteristics and atmospheric state were obtained from two aircraft, a NASA ER-2 and a DC-8. This paper presents a diagnosis of observations obtained using the ER-2 on January 24, 1989, using a Lagrangian coupled microphysical-photochemical model. The high chlorine monoxide mixing ratios observed from the ER-2 on the afternoon of January 24, 1989 are interpreted as a result of in situ heterogeneous release of reactive chlorine from the reservoirs HCl and CIONO2 on type-1 polar stratospheric cloud particles observed to be present at that time. This essential element in theories of polar ozone depletion has never before been observed directly in the stratosphere.

Jones, R. L.↗

NASA NTRS1990

On the influence of polar stratospheric cloud formation on chemical composition during the 1988/89 Arctic winter

The northern winter polar vortex is more disturbed dynamically and warmer than the Antarctic equivalent, and correspondingly fewer polar stratospheric clouds (PSCs) are observed to form. However, the rapid flow of stratospheric air through slow moving synoptically forced PSC regions can result in exposure of both vortical and extra vortical air to PSCs intermittently throughout the winter months. This periodic exposure to PSCs may be sufficient to perturb the chemical composition of large volumes of nothern hemisphere air. The synoptic forcing also leads to marked meridional flow which has a profound effect on chemical composition, having major impacts on both short term ozone depletion and the longer term recovery to lower ClOx abundances. Accurate simulation of the air flow is thus essential for the reliable calculation of ozone loss in polar regions.

Jones, R. L.↗

NASA NTRS1990

Simulating the evolution of the chemical composition of the 1988/89 winter vortex

During the 1988/89 Airborne Arctic Stratospheric Expedition (AASE) observations of the chemical composition and aerosol characteristics of the winter vortex were obtained from a NASA ER-2 aircraft. In this paper we present interpretations of observations obtained on three ER-2 flights using a Lagrangian coupled photochemical-microphysical model. It is argued that observations obtained on Jaunary 16 and 19, and February 10, represent different stages of the chemical evolution of the vortex, from the early stages of chlorine release, the onset of denitrification and the intensively processed state.

Jones, R. L.↗

NASA NTRS1990

Homogeneous and heterogeneous chemistry along air parcel trajectories

The study of coupled heterogeneous and homogeneous chemistry due to polar stratospheric clouds (PSC's) using Lagrangian parcel trajectories for interpretation of the Airborne Arctic Stratosphere Experiment (AASE) is discussed. This approach represents an attempt to quantitatively model the physical and chemical perturbation to stratospheric composition due to formation of PSC's using the fullest possible representation of the relevant processes. Further, the meteorological fields from the United Kingdom Meteorological office global model were used to deduce potential vorticity and inferred regions of PSC's as an input to flight planning during AASE.

Jones, R. L.↗

NASA NTRS1990

Polar ozone

The observation and interpretation of a large, unexpected ozone depletion over Antarctica has changed the international scientific view of stratospheric chemistry. The observations which show the veracity, seasonal nature, and vertical structure of the Antarctic ozone hole are presented. Evidence for Arctic and midlatitude ozone loss is also discussed. The chemical theory for Antarctic ozone depletion centers around the occurrence of polar stratospheric clouds (PSCs) in Antarctic winter and spring; the climatology and radiative properties of these clouds are presented. Lab studies of the physical properties of PSCs and the chemical processes that subsequently influence ozone depletion are discussed. Observations and interpretation of the chemical composition of the Antarctic stratosphere are described. It is shown that the observed, greatly enhanced abundances of chlorine monoxide in the lower stratosphere are sufficient to explain much if not all of the ozone decrease. The dynamic meteorology of both polar regions is given, interannual and interhemispheric variations in dynamical processes are outlined, and their likely roles in ozone loss are discussed.

Solomon, S.↗

NASA NTRS1989

OH-asterisk (7-5) Meinel band dayglow and nightglow measured by the SME limb scanning near infrared spectrometer - Comparison of the observed seasonal variability with two-dimensional model simulations

Seasonal variations of the OH-asterisk (7-5) mesospheric hydroxyl emission at 1.89 microns observed by the SME near-IR spectrometer are compared with the theoretical predictions of a two-dimensional dynamical/chemical model. The good agreement found at low latitudes for both dayglow and nightglow provides support for the model assumption that breaking gravity waves induce seasonal and latitudinal variations in diffusion. The seasonal behavior of atomic hydrogen in the upper mesosphere (related to vertical transport) and/or uncertainties in the OH Meinel band parameters are proposed as possible explanations for the discrepancy noted between model and observational data for the middle latitudes.

Le Texier, H.↗

NASA NTRS1989

Observations and theories related to Antarctic ozone changes

In 1985, there was a report of a large, sudden, and unanticipated decrease in the abundance of springtime Antarctic ozone over the last decade. By 1987, ozone decreases of more than 50 percent in the total column, and 95 percent locally between 15 and 20 km, had been observed. The scientific community quickly rose to the challenge of explaining this remarkable discovery; theoreticians soon developed a series of chemical and dynamical hypotheses to explain the ozone loss. Three basic theories were proposed to explain the springtime ozone hole. (1) The ozone hole is caused by the increasing atmospheric loadings of manmade chemicals containing chlorine (chlorofluorocarbons (CFC's) and bromine (halons)). These chemicals efficiently destroy ozone in the lower stratosphere in the Antarctic because of the special geophysical conditions, of an isolated air mass (polar vortex) with very cold temperatures, that exist there. (2) The circulation of the atmosphere in spring has changed from being predominantly downward over Antarctica to upward. This would mean that ozone poor air from the troposphere, instead of ozone rich air from the upper stratosphere, would be transported into the lower Antarctic stratosphere. (3) The abundance of the oxides of nitrogen in the lower Antarctic stratosphere is periodically enhanced by solar activity. Nitrogen oxides are produced in the upper mesosphere and thermosphere and then transported downward into the lower stratosphere in Antarctica, resulting in the chemical destruction of ozone. The climatology and trends of ozone, temperature, and polar stratospheric clouds are discussed. Also, the transport and chemical theories for the Antarctic ozone hole are presented.

Hartmann, D.↗

NASA NTRS1988

Ground-based measurements of O3, NO2, OClO, and BrO during the 1987 Antarctic ozone depletion event

Near-ultraviolet absorption spectroscopy in the wavelength range from 330 to 370 nm was used to measure O3, NO2, OClO, and BrO at McMurdo Station (78S) during 1987. Visible absorption measurements of O3, NO2, and OClO were also obtained using the wavelength range from about 403 to 453 nm. These data are described and compared to observations obtained in 1986. It is shown that comparisons of observations in the two wavelength ranges provide a sensitive measure of the altitude where the bulk of atmospheric absorption takes place.

Sanders, R. W.↗

NASA NTRS1988

Observations of diurnal variations of BrO and OClO at McMurdo Station, Antarctica (78S)

Observations of the diurnal variations of OClO and BrO during austral spring, 1987 using long-path visible and near-ultraviolet absorption spectroscopy are presented and compared to simplified model calculations. It is shown that care must be taken to compare model calculations and measurements along the line of sight of the instrument. Evening twilight observations of OClO are shown to be broadly consistent with current photochemical schemes, assuming ClO and BrO levels near 50 mb of about 0.5 ppbv and 7 pptv, respectively, throughout the observing period from late Aug. to mid-Oct. Nighttime observations of OClO obtained using the moon as a light source display evidence for growth through the night in late-Aug., but not in late-Sept. Further, the observed morning twilight OClO abundances are in agreement with model calculations in late August, but generally fall below in late September and October. Observations of BrO in mid-Sept. systematically show far greater evening twilight than morning twilight abundances.

Solomon, S.↗

NASA NTRS1988

Visible and near-ultraviolet spectroscopy at Thule AFB (76.5 N) from January 28 - February 15, 1988

Near-ultraviolet and visible spectrographs identical to those employed at McMurdo Station, Antarctica (77.8 S) during the austral spring seasons of 1986 and 1987 were used to study the stratosphere above Thule, Greenland (76.5 N) during early spring, 1988. Observations were carried out both at night using the direct moon as a light source, and during the day by collecting the scattered light from the zenith sky when solar zenith angles were less than about 94.5 degrees. Excellent meteorological conditions prevailed in the troposphere and stratosphere at Thule. Surface weather was extremely clear over most of the period, facilitating measurements of the direct light from the moon. The lower stratospheric arctic polar vortex was located very near Thule throughout the observing period, and temperature at the 30 mbar level were typically below -80 C above Thule, according to the National Meteorological Center daily analyses. Thus conditions were favorable for polar stratospheric cloud formation above Thule. Total column ozone abundances were about 350 to 400 Dobson units, and did not suggest a clear temporal trend over the observing period. Stratospheric nitrogen dioxide measurements were complicated by the presence of a large component of tropospheric pollution on many occasions. Stratospheric nitrogen dioxide could be identified on most days using the absorption in the scattered light from the zenith sky, which greatly enhances the stratospheric airmass while suppressing the tropospheric contribution. These measurements suggest that the total vertical column abundance of nitrogen dioxide present over Thule in February was extremely low, sometimes as low as 3 x 10 to the 14th per sq cm. The abundance of nitrogen dioxide increased systemically from about 3 x 10 to the 14th in late January to 1.0 x 10 to the 15th per sq cm in mid-February, perhaps because of photolysis of N2O5 in the upper part of the stratosphere, near 25 to 35 km.

Mount, G. H.↗

NASA NTRS1988

The role of molecular hydrogen and methane oxidation in the water vapour budget of the stratosphere

The detailed photochemistry of methane oxidation has been studied in a coupled chemical/dynamical model of the middle atmosphere. The photochemistry of formaldehyde plays an important role in determining the production of water vapor from methane oxidation. At high latitudes, the production and transport of molecular hydrogen is particularly important in determining the water vapor distribution. It is shown that the ratio of the methane vertical gradient to the water vapor vertical gradient at any particular latitude should not be expected to be precisely 2, due both to photochemical and dynamical effects. Modeled H2O profiles are compared with measurements from the Limb Infrared Monitor of the Stratosphere (LIMS) experiment at various latitudes. Molecular hydrogen is shown to be responsible for the formation of a secondary maximum displayed by the model water vapor profiles in high latitude summer, a feature also found in the LIMS data.

Le Texier, H.↗

NASA NTRS1987

Seasonal variability of the OH Meinel bands

The influence of seasonal and latitudinal changes in the distribution of mesospheric components on the OH Meinel-band nightglow is investigated by means of numerical simulations using the two-dimensional dynamical/chemical model of Garcia and Solomon (1985). The processes responsible for the formation and destruction of vibrationally excited OH in the mesosphere are described; the seasonal/latitudinal evolution for the higher (v greater than 6) and lower (v = 1-6) levels is shown in graphs and maps and characterized in detail; and the theoretical results are compared with published observational data. The lower-level emission is shown to depend on both O and H, suggesting that the variation of the Meinel-band nightglow can provide important information on the roles of advection and diffusion in the transport of water vapor and odd oxygen near the mesopause.

Le Texier, H.↗

NASA NTRS1987

Mesospheric ionization and O2 1Delta(g) depletion

Observations of O2 1Delta(g) emission during solar proton events reveal large depletions below 80 and near 90 km. The lower-altitude depletions are believed to be due to odd hydrogen production and associated depletion of ozone, but the mechanism producing the depletion near 90 km has not yet been established. In this paper, it is proposed that an exothermic charge exchange reaction between O2(+) and O2 1Delta(g) is likely to be responsible for these high-altitude depletions. In particular, it is shown that the vertical structure of the observed change in airglow emission is consistent with this mechanism.

Spear, K. A.↗

NASA NTRS1987

Joule heating in the mesosphere and thermosphere during the July 13, 1982, solar proton event

The solar proton event of July 13, 1982 produced considerable ionization in the polar-cap mesosphere. Energetic solar proton fluxes were measured by the NOAA-6 satellite. The DE-2 satellite measured the low-energy electrons, the ion drift velocity, and other atmospheric and ionospheric properties during the event in the region of the measured maximum electric field (189 mV/m at 2215 UT near 60 deg N), a Joule heating rate of 1-3 K/day is calculated between 70 and 80 km, exceeding the heating due to ozone absorption at noon in the summer hemisphere in that altitude range. The Joule heating rate above 90 km greatly exceeded 20 K/day. The calculated height-integrated Joule heating rate above 100 km in the same region exceeded 400 ergs/sq cm sec, and DE-2 near 350 km measured neutral winds of nearly 1000 m/s and neutral gas temperatures of over 2000 K. The overall ionospheric structure calculated below the DE-2 satellite is described.

Roble, R. G.↗

NASA NTRS1987

Martian surface physical properties to be derived by radar altimeter on the Mars observer spacecraft

The potential is described of a candidate Mars Observer altimeter for determining dielectric properties of Mars regolith. It is pointed out that it is straightforward to use the time between altimeter pulse trains for passive radiometry (hence dielectric properties) and roughness can be derived. Given the mission plan the whole surface can be mapped at least three times, yielding data on seasonal variability.

Garvin, J. B.↗