Photochemistry of nitrogen in the Martian atmosphere

Models are developed for the photochemistry of a CO₂H₂ON₂ atmosphere on Mars and estimates are given for the concentrations of N, NO, NO₂, NO₃, N₂O₅, HNO₂, HNO₃, and N₂O as a function of altitude. Nitric oxide is the most abundant form of odd nitrogen, present with a mixing ratio relative to CO₂ of order 10^?8. Deposition rates for nitrite and nitrate minerals could be as large as 3× 10⁵ N equivalent atoms cm^?2 sec^?1 under present conditions and may have been higher in the past.     

Oxidation state of the atmosphere and crust of Venus from pioneer Venus results

Recent spacecraft observations of Venus permit a detailed model of sulfur chemistry in the atmosphere-lithosphere system. Pioneer Venus experiments confirm that, as predicted, COS and H₂S are dominant over SO₂ in the lower atmosphere, and that the equilibrium concentrations of S₂ and S₃ are significant. Many criteria serve to bracket the oxidation state of the crust: it is nearly certain that the S₂^2?/SO₄^2? buffer regulates the oxygen fucagity, and that FeO is at least as abundant as Fe₂O₃ in crustal silicates. A highly oxidized crust (as, for example, would result from O₂ absorption complementary to escape of vast amounts of H₂) is incompatible with the gas-phase sulfur chemistry. If the Pioneer Venus mass spectrometer estimates of the abundance of sulfur gases are correct, Earth-like models for the bulk composition of Venus are seriously in error, and a far lower FeO content is required for Venus.     

S.E.M.A.Ph.Or.E COMETAIRE,a tool for the study of the photochemical decomposition of probable large organic molecules in comets. first application: Polyoxymethylene

This paper presents a current experimental program concerning the study of the photochemical evolution of the organic matter ejected from the cometary nucleus. The aim of the work is to better understand, using laboratory simulations, the mechanisms which are involved in the degradation of the high molecular weight organics in cometary ices and dust when they are submitted to the warming up and to the bombardment of photons in the surrounding area of the Sun. This experimental study will establish correlations between the nucleus and the molecular composition of the coma. Furthermore, experimental data will provide useful information to bring to a close the question of the origin of the extended sources of H₂CO and CO. Polyoxymethylene, suspected to be present in the cometary nucleus, is often mentioned as a possible parent molecule for the extended source of H₂CO. In order to test this hypothesis, irradiation of POM has been performed at 147 nm. The preliminary results show effectively H₂CO as one photodegradation product as well as CO. C0₂ and HCOOH. Tentative detections of CH₃0CH₃, CH₃OCH₂OCH₃, CH₃OCHO and C₃H₆O₃ are also presented.     

Relationships among some parameters of GPS radio sources

Data on the parameters of the complete sample of gigahertz-peaked spectrum (GPS) radio sources available in the literature are analyzed to find statistical relationships among them. Correlations are found among the following parameters: l)flux density S_m at the turnover point of the spectrum as a function of the corresponding observed frequency v_m; 2) the turnover frequency v_rest in a fixed coordinate system as a function of the linear size LS in projection; 3 the linear size LS in projection as a function of redshift z; 4 the flux density S_m at the turnover point of a galaxy’s GPS as a function of the corresponding linear size LS in projection. Translated from Astrofizika, Vol. 42, No. 4, pp. 589–595, October–December, 1999.     

Fabrication and response of high concentration SIMPLE superheated droplet detectors with different liquids

The combined measurement of dark matter interactions with different superheated liquids has recently been suggested as a cross-correlation technique in identifying WIMP candidates. We describe the fabrication of high concentration superheated droplet detectors based on the light nuclei liquids C₃F₈, C₄F₈, C₄F₁₀ and CCl₂F₂, and investigation of their irradiation response with respect to C₂ClF₅. The results are discussed in terms of the basic physics of superheated liquid response to particle interactions, as well as the necessary detector qualifications for application in dark matter search investigations. The possibility of heavier nuclei SDDs is explored using the light nuclei results as a basis, with CF₃I provided as an example.     

The role of hydrocarbons in the lonospheres of the outer planets

The role of hydrocarbons as a possible sink for H⁺ and H₃⁺ ions in the lower ionosphere of the outer planets is examined. Calculations indicate that H⁺ and H₃⁺ are efficiently converted to hydrocarbon ions on reaction with methane. The terminal ions, CH₅⁺ and C₂H₅⁺ are rapidly neutralized in dissociative recombination with electrons. Extreme ultraviolet photolysis of hydrocarbons as a potential additional source of lower elevation ions in investigated.     

The Martian paleoclimate and enhanced atmospheric carbon dioxide

Current evidence indicates that the Martian surface is abundant with water presently in the form of ice, while the atmosphere was at one time more massive with a past surface pressure of as much as 1 atm of CO₂. In an attempt to understand the Martian paleoclimate, we have modeled a past CO₂H₂O greenhouse and find global temperatures which are consistent with an earlier presence of liquid surface water, a finding which agrees with the extensive evidence for past fluvial erosion. An important aspect of the CO₂H₂O greenhouse model is the detailed inclusion of CO₂ hot bands. For a surface pressure of 1 atm of CO₂, the present greenhouse model predicts a global mean surface temperature of 294°K, but if the hot bands are excluded, a surface temperature of only 250°K is achieved.     

A hydrocode equation of state for SiO2

Abstract— The thermodynamic properties of SiO₂ are approximated over a range of pressures and temperatures important under the extreme conditions achieved in impacts at typical solar system velocities from 5 to about 70 km/s. The liquid/vapor phase curve and critical point of SiO₂ are computed using the equation of state (EOS) program ANEOS. To achieve this goal, two shortcomings of ANEOS are corrected. ANEOS, originally developed at Sandia National Laboratories to describe metals, treats the vapor phase as a monatomic mixture of atoms, rather than molecular clusters. It also assumes a Morse potential for the expanded solid state. Neither of these assumptions is accurate for geologic materials, such as SiO₂, that contain molecular clusters in the vapor phase and are better described by a Mie‐type potential in the solid state. Using the updates described here, an EOS adequate for numerical hydrocode computations is constructed that agrees well with shock data at pressures up to at least 600 GPa and temperatures up to 50,000 K. This EOS also gives a good representation of the liquid/vapor transition at much lower pressures and temperatures. The estimated critical point parameters for SiO₂ are P_c = 0.19 GPa, T_c = 5400K, ρ_c = 550 kg/m³.     

Effects of ion excitation on charge transfer reactions of the Mars, Venus, and Earth ionospheres

The absolute reaction cross sections and reaction rate coefficients as a function of photoionisation energy for 25 ion-molecule reactions (charge transfer reactions except for one) have been measured between the most abundant species present as ions or neutral in the Mars, Venus and Earth ionospheres: O₂, N₂, NO, CO, Ar and CO₂.This study shows the strong influence of electronic as well as vibrational internal energy on most ion-molecule reactions. In particular endothermic charge transfer reactions are driven by electronic excitation of O₂⁺ and NO⁺ ions in their a⁴Π_u and a³Σ⁺ metastable states, respectively. Moreover, it is shown that lifetimes of these metastable states are sufficient to survive the mean free path in the lowest part of ionospheres and therefore express their enhanced reactivity. The reactions of O₂⁺ with NO as well as the reactions of CO₂⁺ with NO, O₂, CO and to a less extent N₂ are driven by vibrational excitation. N₂⁺ and CO⁺ reactions vary much less with photon energy than the other ones, except for the case of reactions with Ar. The effects of the molecular ion internal energy content on their reactivity must be included in the ionospheric models for most of the reactions investigated in the present work. It is also the case for the effect of collision energy on the CO⁺+M reactions as we expect that a significant proportion of these CO⁺ could be produced with translational energy by dissociation of doubly charged CO₂²⁺, in particular in the Mars ionosphere. Recommended effective rate constant values are given as a function of VUV photon energy.     

On the accuracy of line-of-sight velocity measurements using telluric lines as reference lines

It is demonstrated that telluric lines H₂O and O₂ are displaced as much as 0.2 mÅ as the solar disk is being scanned. The temporal variations of such displacements have a quasi-periodic character.     

Petrology and geochemistry of the Elephant Moraine A79002 diogenite: A genomict breccia containing a magnesian harzburgite component

Abstract— The Elephant Moraine A79002 (EETA79002) diogenite is a fragmental breccia with a subtle lightdark structure. It is composed of orthopyroxene, with minor olivine, chromite, and ubiquitous, inhomogeneously distributed, approximately 5–500 μm sized troilite and metal grains. These latter are present in the matrix, and as inclusions in and as symplectic intergrowths with orthopyroxene and olivine. Trace amounts of silica and diopside are also present. Most orthopyroxene compositions (typical orthopyroxenes) are in the narrow range Wo_2.1–2.7En_74.1–75.6Fs_22.2–23.8 like those of most diogenites. A few magnesian orthopyroxenes are present with compositions of Wo_1.7‐2.5En_77.5–80.2 Fs_18.2–20.3. These are among the most magnesian orthopyroxenes known from diogenites. A few ferroan orthopyroxenes have compositions of Wo_2.1–2.9En_71.7–73.7Fs_24.2–25.5. Differences in Al₂O₃, TiO₂, and Cr₂O₃ between the different orthopyroxene groups are inconsistent with a simple igneous fractionation relationship between them. Olivine compositions are Fo_75.0–76.9. The olivines could be in equilibrium with the magnesian orthopyroxenes, but not with the typical or ferroan orthopyroxenes that form the bulk of EETA79002. Metal grains exhibit a range of Ni and Co contents and Ni/Co ratios; their compositions indicate that they are primary igneous metal. Metal and troilite grains are more prevalent in the dark samples. The trace incompatible lithophile element contents of 16 samples are remarkably uniform. Their Yb concentrations are all within their 2s? analytical uncertainties of the mean. The uniformity and low content of light rare earth elements in EETA79002 indicate that negligible amounts of a trapped liquid component, or foreign material mixed in the breccia, could be present. The siderophile and chalcophile element data show that the light‐dark structure is due to the distribution of metal and troilite grains; dark samples contain higher Ni, Co, and Se compared to light samples. Meteorite EETA79002 appears to contain material from three or more related plutons, a magnesian harzburgite, and two orthopyroxenites, and is a genomict breccia.     

Laboratory studies on the reactions between Chlorine,Sulfur Dioxide,and Oxygen: Implications for the Venus Stratosphere

The title reaction was studied by photolyzing mixtures of Cl₂ and SO₂ with and without O₂ present in an atmosphere of N₂, using Fourier transform infrared spectrophotometry to monitor reactants and products. In the absence of oxygen, sulfur dioxide is quantitatively converted to sulfuryl chloride. With 10 to 150 Torr O₂ present H₂SO₄ is produced as well as SO₂Cl₂. When a number of speculative reactions inferred from these experiments are added to a published model for Venus stratospheric chemistry, it emerges that SO₂Cl₂ is a key reservoir species for chlorine and that the reaction between Cl and So₂ provides an important cycle for destroying O₂ and converting SO₂ to H₂So₄. The modified model could provide a possible solution to the photochemistry of the Venus stratosphere if the mixing ratio of chlorine on Venus were as high as 8 ppm.     

Atmospheric Chemistry in Giant Planets, Brown Dwarfs, and Low-Mass Dwarf Stars: I. Carbon, Nitrogen, and Oxygen

The chemical species containing carbon, nitrogen, and oxygen in atmospheres of giant planets, brown dwarfs (T and L dwarfs), and low-mass stars (M dwarfs) are identified as part of a comprehensive set of thermochemical equilibrium and kinetic calculations for all elements. The calculations cover a wide temperature and pressure range in the upper portions of giant planetary and T-, L-, and M-dwarf atmospheres. Emphasis is placed on the major gases CH₄, CO, NH₃, N₂, and H₂O but other less abundant gases are included. The results presented are independent of particular model atmospheres, and can be used to constrain model atmosphere temperatures and pressures from observations of different gases. The influence of metallicity on the speciation of these key elements under pressure-temperature (P-T) conditions relevant to low-mass object atmospheres is discussed. The results of the thermochemical equilibrium computations indicate that several compounds may be useful to establish temperature or pressure scales for giant planet, brown dwarf, or dwarf star atmospheres. We find that ethane and methanol abundance are useful temperature probes in giant planets and methane dwarfs such as Gl 229B, and that CO₂ can serve as a temperature probe in more massive objects. Imidogen (NH) abundances are a unique pressure-independent temperature probe for all objects. Total pressure probes for warmer brown dwarfs and M dwarfs are HCN, HCNO, and CH₂O. No temperature-independent probes for the total pressure in giant planets or T-dwarf atmospheres are identified among the more abundant C, N, and O bearing gases investigated here.     

Superconducting critical field in cold magnetic white dwarfs and in neutron stars

For an evaluation of the superconducting critical fieldH _c as a function of the mass-density in the external layers of cold magnetic white dwarfs and in the superconducting proton fluid in neutron stars, we use the solution of a differential equation involvingH _c as a function of the pressure. The differential equation and its solution are obtained by pure thermodynamic way.Finally other thermodynamic quantities are calculated for the above superconducting astrophysical systems.     

Mass spectroscopic investigation of dissociation and ionization in a simulated re-entry plasma

With a new type of a miniaturized fourfold monopole mass spectrometer the hypersonic flow around suitable model targets is investigated and gaseous reactions studied. Flow parameters are chosen such as to simulate the re-entry conditions of a spacecraft returning into the Earth's atmosphere. The dissociation of N₂ and O₂ is measured in the flow around a half sphere as well as in the stagnation point. Under the given condition the degree of ionization of N₂ never reached the sensitivity limit of 5 per cent. O₂, however, was always dissociated to a measurable degree at the stagnation point, while in the flow noticeable dissociation occurred only with small gas density. Theoretical computations are in good agreement with the observed data. Three kinds of ions were found in the stagnation point, NO⁺ abundance as predicted by theory is confirmed for high but not for low pressure.     

High-resolution 3-μm spectra of Jupiter: Latitudinal spectral variations influenced by molecules, clouds, and haze

We present latitudinally-resolved high-resolution (R = 37,000) pole-to-pole spectra of Jupiter in various narrow longitudinal ranges, in spectral intervals covering roughly half of the spectral range 2.86-3.53 μm. We have analyzed the data with the aid of synthetic spectra generated from a model jovian atmosphere that included lines of CH₄, CH₃D, NH₃, C₂H₂, C₂H₆, PH₃, and HCN, as well as clouds and haze. Numerous spectral features of many of these molecular species are present and are individually identified for the first time, as are many lines of and a few unidentified spectral features. In both polar regions the 2.86-3.10-μm continuum is more than 10 times weaker than in spectra at lower latitudes, implying that in this wavelength range the single-scattering albedos of polar haze particles are very low. In contrast, the 3.24-3.53 μm the weak polar and equatorial continua are of comparable intensity. We derive vertical distributions of NH₃, C₂H₂ and C₂H₆, and find that the mixing ratios of NH₃ and C₂H₆ show little variation between equatorial and polar regions. However, the mixing ratios of C₂H₂ in the northern and southern polar regions are ∼6 and ∼3 times, respectively, less than those in the equatorial regions. The derived mixing ratio curves of C₂H₂ and C₂H₆ extend up to the 10⁻⁶ bar level, a significantly higher altitude than most previous results in the literature. Further ground-based observations covering other longitudes are needed to test if these mixing ratios are representative values for the equatorial and polar regions.     

Analysis of Titan's neutral upper atmosphere from Cassini Ion Neutral Mass Spectrometer measurements

In this paper we present an in-depth study of the distributions of various neutral species in Titan's upper atmosphere, between 950 and 1500 km for abundant species (N₂, CH₄, H₂) and between 950 and 1200 km for other minor species. Our analysis is based on a large sample of Cassini/INMS (Ion Neutral Mass Spectrometer) measurements in the CSN (Closed Source Neutral) mode, obtained during 15 close flybys of Titan. To untangle the overlapping cracking patterns, we adopt Singular Value Decomposition (SVD) to determine simultaneously the densities of different species. Except for N₂, CH₄, H₂ and ⁴⁰Ar (as well as their isotopes), all species present density enhancements measured during the outbound legs. This can be interpreted as a result of wall effects, which could be either adsorption/desorption of these molecules or heterogeneous surface chemistry of the associated radicals on the chamber walls. In this paper, we provide both direct inbound measurements assuming ram pressure enhancement only and abundances corrected for wall adsorption/desorption based on a simple model to reproduce the observed time behavior. Among all minor species of photochemical interest, we have firm detections of C₂H₂, C₂H₄, C₂H₆, CH₃C₂H, C₄H₂, C₆H₆, CH₃CN, HC₃N, C₂N₂ and NH₃ in Titan's upper atmosphere. Upper limits are given for other minor species.The globally averaged distributions of N₂, CH₄ and H₂ are each modeled with the diffusion approximation. The N₂ profile suggests an average thermospheric temperature of 151 K. The CH₄ and H₂ profiles constrain their fluxes to be and , referred to Titan's surface. Both fluxes are significantly higher than the Jeans escape values. The INMS data also suggest horizontal/diurnal variations of temperature and neutral gas distribution in Titan's thermosphere. The equatorial region, the ramside, as well as the nightside hemisphere of Titan appear to be warmer and present some evidence for the depletion of light species such as CH₄. Meridional variations of some heavy species are also observed, with a trend of depletion toward the north pole. Though some of the above variations might be interpreted by either the solar-driven models or auroral-driven models, a physical scenario that reconciles all the observed horizontal/diurnal variations in a consistent way is still missing. With a careful evaluation of the effect of restricted sampling, some of the features shown in the INMS data are more likely to be observational biases.     

The effect of ammonia ice on the outgoing thermal radiance from the atmosphere of Jupiter

We examine the effects of NH₃ ice particle clouds in the atmosphere of Jupiter on outgoing thermal radiances. The cloud models are characterized by a number density at the cloud base, by the ratio of the scale height of the vertical distribution of particles (H_p) to the gas scale height (H_g), and by an effective particle radius. NH₃ ice particle-scattering properties are scaled from laboratory measurements. The number density for the various particle radius and scale height models is inferred from the observed disk average radiance at 246 cm^?1, and preliminary lower limits on particle sizes are inferred from the lack of apparent NH₃ absorption features in the observed spectral radiances as well as the observed minimum flux near 2100 cm^?1. We find lower limits on the particle size of 3 μm if H_p/H_g = 0.15, or 10μmif H_p/H_g = 0.50 or 0.05. NH₃ ice particles are relatively dark near the far-infrared and 8.5-μm atmospheric windows, and the outgoing thermal radiances are not very sensitive to various assumptions about the particle-scattering function as opposed to radiances at 5 μm, where particles are relatively brighter. We examined observations in these three different spectral window regions which provide, in principle, complementary constraints on cloud parameters. Characterization of the cloud scale height is difficult, but a promising approach is the examination of radiances and their center-to-limb variation in spectral regions where there is significant opacity provided by gases of known vertical distribution. A blackbody cloud top model can reduce systematic errors due to clouds in temperature sounding to the level of 1K or less. The NH₃ clouds provide a substantial influence on the internal infrared flux field near the 600-mbar level.     

Regularization and linearization of the equations of motion in central force-fields

Within the framework of linear and regular celestial mechanics, a wide class of central force field problems are considered. We take as potential function a polynomial whose variable is the reciprocal of the distance from the origin, and, as regularizing function the square root of a certain reciprocal polynomial, related to the potential function. The relations between the coefficients of both functions, in order to arrive to linear equations, are given. In particular, the case of a quintic polynomial is analyzed, and an application is made to artificial earth satellites considering harmonicsJ ₂,J ₃,J ₄.