A measurement of the O2 ultra-violet nightglow emission

New measurements of the Herzberg I emission height profile in the night airglow are reported and indicate a peak emission height near 96 km in agreement with previous measurements. Using an atomic oxygen concentration profile determined from the oxygen green line profile measured on the same rocket it is concluded that the O₂(A³Σ_u⁺) state is not excited in the direct three body recombination of atomic oxygen. It is suggested that the excitation mechanism is a two step process, similar to the Barth mechanism for the atomic oxygen green lineand that the excited intermediate state is C³Δ_u.     

The excitation of O2(b1Σg+) in the nightglow

It is proposed that the available measurements of the O₂(b¹Σ_g⁺ ?X³Σ_g^?) atmospheric bands both in the nightglow and in the laboratory indicate that the excitation mechanism is a two-step process rather than the direct three body recombination of atomic oxygen. It is shown that such a two-step mechanism can explain observations of the atmospheric bands both in altitude and intensity.     

The altitude dependence of the O2(A3Σu+) vibrational distribution in the terrestrial nightglow

A simple vibrational relaxation model which reproduces the observed altitude integrated vibrational distribution of the Herzberg I bands in the nightglow is used to derive the altitude profiles of the individual vibrational levels at 1 km intervals in the 85–115 km height range. The possible errors associated with using rocket-borne photometer measurements of a limited number of bands in the O₂(A³Σ_u⁺?X³Σ_g^?) system to infer the total Herzberg I emission profile are assessed.     

ETON 6: A rocket measurement of the O2 Infrared Atmospheric (0-0) band in the nightglow

Co-ordinated rocket measurements of the O₂(a¹Δ_g−X³Σ_g⁻) Infrared Atmospheric (0-0) band emission profile and the atomic oxygen densities in an undisturbed night-time atmosphere are used to investigate the processes responsible for the excitation of O₂(a¹Δ_g) in the terrestrial nightglow. It is shown that three-body recombination of atomic oxygen, and subsequent energy transfer processes, can explain only part of the observed emission profile and that at least two other sources of O₂(a¹Δ_g) emission must exist. One of these additional sources, responsible for most of the emission observed below 90km, is identified as arising from the night-time residual of the very large dayglow ¹Δ_g population. The other additional source is required to explain most of the emission observed above 95km. The processes responsible for this high altitude component cannot be identified but the vertical distribution of the required source function strongly resembles the profile of the atomic oxygen density squared and suggests that a two-body radiative recombination process may be involved. However, the measured zenith emission rates can also be explained without the high altitude source of O₂(a¹Δ_g) if optical emission at 1.27 μm was induced by the rocket as it penetrated the nightglow layer.     

Radiation chemistry of H2O + O2 ices

The chemistry and spectroscopy of proton-irradiated H₂O + O₂ ices have been investigated in relation to the production of oxidants in icy satellite surfaces. Hydrogen peroxide (H₂O₂), ozone (O₃), and the hydroperoxy (HO₂) and hydrogen trioxide (HO₃) radicals have all been observed, and their temperature and dose dependent production trends have been measured. We find that O₂ aggregates form during the growth of H₂O + O₂ ice films, and the presence of these aggregates greatly affects the HO₂ and H₂O₂ yields. In addition, we have found that the position of the spectral maximum of the ν₃ vibration of O₃ shifts with ice composition, giving an indication of the degree of dispersion of O₃ molecules within the ice. We discuss the relevance of these measurements to icy satellite surfaces.     

Brightness of the O2 atmospheric bands in the daytime thermosphere

The Fabry-Perot interferometer on Dynamics Explorer 2 was used as a low sensitivity photometer to study the O₂ Atmospheric A band during the daytime. A study of the brightness of the emission showed that the assumed source of O₂(b¹Σ_g⁺) in the thermosphere, O(¹D), can account for the observed intensity up to about 250 km but with a significantly different scale height. This combined with an enhanced brightness above this altitude suggests an additional source for this emission.     

The spatial morphology of Europa's near-surface O2 atmosphere

Results from a three-dimensional ballistic model of Europa's O₂ atmosphere are presented. Hubble Space Telescope (HST) ultraviolet observations show spatially non-uniform O₂ airglow from Europa. One explanation for this is that the O₂ atmosphere is spatially non-uniform. We show that non-uniform ejection of O₂ alone cannot reproduce the required morphology, but that a non-uniform distribution of reactive species in Europa's porous regolith can result in a non-uniform O₂ atmosphere. By allowing O₂ molecules to react with Europa's visibly dark surface material, we produced a spatially non-uniform atmosphere which, assuming uniform electron excitation of O₂ over the trailing hemisphere, compares favorably with the morphology suggested by the HST observations. This model, which requires a larger source of O₂ than has previously been estimated, can in principal be tested by the New Horizons observations of Europa's O₂ atmosphere.     

Energy transfer from excited N2 and O2 as a source of O(1S) in the Aurora

It is proposed that energy transfer from excited O₂ contributes to the production of O(¹S) in aurora. An analysis is presented of the OI5577 Å emission in an IBC II⁺ aurora between 90 and 130 km. The volume emission rate of the emission at these altitudes is consistent with the production rate of O(¹S) by energy transfer to O(³P) from N₂ in the A³Σ₂⁺ state and O₂ in the A³Σ_u⁺, C³Δc¹Σ_u^? states, the N₂A state being populated by direct electron impact excitation and B → A cascade and the excited O₂ states by direct excitation. Above the peak emission altitude (~105 km), energy transfer from N₂A is the predominant production mechanism for O(¹S). Below it, the contribution from quenching of the O₂ states becomes significant.     

Hydrogen peroxide dimers and the production of O2 in icy satellite surfaces

Oxygen is seen in the reflectance spectra of the icy surfaces of Ganymede and Europa via absorption bands at 627 and 573 nm. Here we show that the trapped O₂ associated with these spectral features can be produced via radiation-induced decomposition of hydrogen peroxide dimers contained in hydrogen peroxide inclusions in these icy satellite surfaces.     

Simultaneous measurements of No and No2 in the stratosphere

Simultaneous measurements of NO and NO₂ in the stratosphere leading to an NO_x determination have been performed by means of i.r. absorption spectrometry using the Sun as a source in the 5·2 μm band of NO and in the 6·2 μm band of NO₂. The observed abundance of NO_P peaks at 26 km where it is equal to (4·2 ± 1) × 10⁹ cm^?3. The volume mixing ratio of NO_p was observed to vary from 1·3 × 10^?9 at 20 km to 1·3 × 10^?8 at 34 km.     

Production, ionization and redistribution of O2 in Saturn's ring atmosphere

Molecular oxygen produced by the decomposition of icy surfaces is ubiquitous in Saturn's magnetosphere. A model is described for the toroidal O₂ atmosphere indicated by the detection of and O⁺ over the main rings. The O₂ ring atmosphere is produced primarily by UV photon-induced decomposition of ice on the sunlit side of the ring. Because O₂ has a long lifetime and interacts frequently with the ring particles, equivalent columns of O₂ exist above and below the ring plane with the scale height determined by the local ring temperature. Energetic particles also decompose ice, but estimates of their contribution over the main rings appear to be very low. In steady state, the O₂ column density over the rings also depends on the relative efficiency of hydrogen to oxygen loss from the ring/atmosphere system with oxygen being recycled on the grain surfaces. Unlike the neutral density, the ion densities can differ on the sunlit and shaded sides due to differences in the ionization rate, the quenching of ions by the interaction with the ring particles, and the northward shift of the magnetic equator relative to the ring plane. Although O⁺ is produced with a significant excess energy, is not. Therefore, should mirror well below those altitudes at which ions were detected. However, scattering by ion-molecule collisions results in much larger mirror altitudes, in ion temperatures that go through a minimum over the B-ring, and in the redistribution of both molecular hydrogen and oxygen throughout the magnetosphere. The proposed model is used to describe the measured oxygen ion densities in Saturn's toroidal ring atmosphere and its hydrogen content. The oxygen ion densities over the B-ring appear to require either significant levels of UV light scattering or ion transmission through the ring plane.     

The global distribution of O3 on mars

Models are developed to describe the photochemistry of ozone on Mars. Catalytic reactions involving H, OH and HO₂ play a major role at low latitudes where they ensure a vertical column density for O₃ of less than 2 × 10^?4 cm atm. The source for odd hydrogen (H + OH + HO₂) is relatively smaller at high latitudes in winter due to the small concentrations of H₂O present there at that time. Odd hydrogen is also efficiently removed from the high-latitude winter atmosphere by condensation of H₂O₂. The role of catalytic chemistry is reduced accordingly and the vertical column density of O₃ may be as large as 5.7 × 10^?3 cm atm in accord with earlier observations carried out by Barth and co-workers with instruments on Mariner 9.     

Dayglow emissions of the O2 Herzberg bands and the Rayleigh backscattered spectrum of the earth

Numerous fluorescent emissions from the Herzberg bands of molecular oxygen lie in the spectral region 242–300 nm. This coincides with the wavelength range used by orbiting spectrometers which observe the Rayleigh backscattered spectrum of the earth for the purpose of monitoring the vertical distribution of stratospheric ozone. Model calculations indicate that Herzberg band emissions in the dayglow could provide significant contamination of the ozone measurements if the quenching rate of O₂(A³Σ) is sufficiently small. This is especially true near 255 nm, where the most intense fluorescent emissions relative to the Rayleigh scattered signal are located and where past satellite measurements show a persistent excess radiance above that expected for a pure ozone absorbing and molecular scattering atmosphere. However, very small quenching rates are adequate to reduce the dayglow emission to negligible levels. Available laboratory data have not definitely established the quenching on the rate of O₂(A³Σ) as a function of vibrational level, and such information is required before the Herzberg band contributions can be evaluated with confidence.     

Mesospheric O3, H and H2O at high latitudes: A theoretical model

The high latitude thermosphere is characterized by a large heat input which produces a strong wind field. In a previous work, the modification of the vertical transport mechanisms produced by high latitude horizontal winds was studied and the resulting concentration profiles are used here to study the influence at mesospheric levels. We obtain an improved agreement with experimental measurements. High solar zenithal angles could explain other differences between the high and middle latitude's mesosphere, especially below 80 km, approximately.     

The dissociative recombination of O2+ in the ionosphere

Aeronomical determinations of the dissociative recombination reaction rate coefficient for O₂⁺, α, depend directly on a knowledge of the rate coefficient for the charge exchange of O⁺ with O₂, k. A re-evaluation of the aeronomical determination of α using Atmosphere Explorer satellite data is necessary in the light of a subsequent laboratory measurement of k. The results reported here are in reasonable agreement with laboratory determinations to within the uncertainty of the analysis for night-time conditions. However, for data obtained under sunlit conditions the aeronomical determination differs significantly from the laboratory measurements. The results imply that the state of the O₂⁺ molecule resulting from the major thermospheric processes requires further examination.     

Observations of C2H6 and C2H2 in the stratosphere of Saturn

We have performed high-resolution spectral observations at mid-infrared wavelengths of C₂H₆ (12.16 μm), and C₂H₂ (13.45 μm) on Saturn. These emission features probe the stratosphere of the planet and provide information on the hydrocarbon photochemical processes taking place in that region of the atmosphere. The observations were performed using our cryogenic echelle spectrometer Celeste, in conjunction with the McMath-Pierce 1.5-m solar telescope in November and December 1994. We used Voyager IRIS CH₄ observations (7.67 μm) to derive a temperature profile on the saturnian atmosphere for the region of the stratosphere. This profile was then used in conjunction with height-dependent volume mixing ratios of each hydrocarbon to determine global abundances for ethane and acetylene. Our ground-based measurements indicate abundances of for C₂H₆ (1.0 mbar pressure level), and for C₂H₂ (1.6 mbar pressure level). We also derived new mixing ratios from the Voyager mid-latitude IRIS observations; 8.6±0.9×¹⁰⁻⁶ for C₂H₆ (0.1-3.0 mbar pressure level), and 1.6±0.2×¹⁰⁻⁷ for C₂H₂ (2.0 mbar pressure level).     

Long-term spectroscopic observations of Mars using IRTF/CSHELL: Mapping of O2 dayglow, CO, and search for CH4

Long-term spectroscopic observations of the O₂ dayglow at 1.27 μm result in a map of the latitudinal and seasonal behavior of the dayglow intensity for the full martian year. The O₂ dayglow is a sensitive tracer of Mars' photochemistry, and this map reflects variations of Mars' photochemistry at low and middle latitudes. It may be used to test photochemical models. Long-term observations of the CO mixing ratio have been also combined into the seasonal-latitudinal map. Seasonal and latitudinal variations of the mixing ratios of CO and the other incondensable gases (N₂, Ar, O₂, and H₂) discovered in our previous work are caused by condensation and sublimation of CO₂ to and from the polar regions. They reflect dynamics of the atmosphere and polar processes. The observed map may be used to test global circulation models of the martian atmosphere. The observed global abundances of CO are in reasonable agreement with the predicted variations with the 11-year solar cycle. Despite the perfect observing conditions, methane has not been detected using the IRTF/CSHELL with a 3σ upper limit of 14 ppb. This upper limit does not rule out the value of 10 ppb observed using the Canada-France-Hawaii Telescope and the Mars Express Planetary Fourier Spectrometer.     

Stratospheric in situ measurements of H2SO4 and HSO3 vapors during a volcanically active period

In situ measurements of stratospheric H₂SO₄ and HSO₃vapors using passive chemical ionization mass spectrometry were made in October 1982 after the eruption of volcano El Chichon. Data were obtained between about 20 and 41 km showing [H₂SO₄ + HSO₃] sum concentrations between about 10⁴ and 2 × 10⁵ cm^?3 below 29 km and a steep rise above this altitude. Maximum [H₂SO₄ + HSO₃] values of about 3 × 10⁶ cm^?3 are reached above 35 km.Partial [HSO₃] concentrations increase above 34 km reaching about $\text{4 × 10}{}^5\text{cm}{}^{\mathrm{?3}}$ around 40 km. From the measurements it is concluded that H₂SO₄ and probably HSO₃photolysis have an important influence above 34 km leading to the observed increase of [HSO₃] and a depletion of H₂SO₄vapor.It also seems that the data support the view of heterogeneous HSO₃ removal. If correct, this would imply that stratospheric aerosols are formed primarily from HSO₃ rather than H₂SO₄vapor.