Atomic oxygen distribution in the Venus mesosphere from observations of O2 infrared airglow by VIRTIS-Venus Express

This VIRTIS instrument on board Venus Express has collected spectrally resolved images of the Venus nightside limb that show the presence of the (0,0) band of the infrared atmospheric system of O₂ at 1.27 μm. The emission is produced by three-body recombination of oxygen atoms created by photodissociation of CO₂ on the dayside. It is consistently bright so that emission limb profiles can be extracted from the images. The vertical distribution of O₂() may be derived following Abel inversion of the radiance limb profiles. Assuming photochemical equilibrium, it is combined with the CO₂ vertical distribution to determine the atomic oxygen density. The uncertainties on the O density caused by the Abel inversion reach a few percent at the peak, increasing to about 50% near 120 km. We first analyze a case when the CO₂ density was derived from a stellar occultation observed with the SPICAV spectrometer simultaneously with an image of the O₂ limb airglow. In other cases, an average CO₂ profile deduced from a series of ultraviolet stellar occultations is used to derive the O profile, leading to uncertainties on the O density less than 30%. It is found that the maximum O density is generally located between 94 and 115 km with a mean value of 104 km. It ranges from less than 1×¹⁰¹¹ to about 5×¹⁰¹¹ cm⁻³ with a global mean of 2.2×¹⁰¹¹ cm⁻³. These values are in reasonable agreement with the VIRA midnight oxygen profile. The vertical O distribution is generally in good agreement with the oxygen profile calculated with a one-dimensional chemical-diffusive model. No statistical latitudinal dependence of the altitude of the oxygen peak is observed, but the maximum O density tends to decrease with increasing northern latitudes. The latitudinal distribution at a given time exhibits large variations in the O density profile and its vertical structure. The vertical oxygen distribution frequently shows multiple peaks possibly caused by waves or variations in the structure of turbulent transport. It is concluded that the O₂ infrared night airglow is a powerful tool to map the distribution of atomic oxygen in the mesosphere between 90 and 115 km and improve future Venus reference atmosphere models.     

Spectral properties and composition of potentially hazardous Asteroid (99942) Apophis

The known close approach of Asteroid (99942) Apophis in April 2029 provides the opportunity for the case study of a potentially hazardous asteroid in advance of its encounter. The visible to near-infrared (0.55 to 2.45 μm) reflectance spectrum of Apophis is compared and modeled with respect to the spectral and mineralogical characteristics of likely meteorite analogs. Apophis is found to be an Sq-class asteroid that most closely resembles LL ordinary chondrite meteorites in terms of spectral characteristics and interpreted olivine and pyroxene abundances, although we cannot rule out some degree of partial melting. A meteorite analog allows some estimates and conjectures of Apophis' possible range of physical properties such as the grain density and micro-porosity of its constituent material. Composition and size similarities of Apophis with (25143) Itokawa suggest a total porosity of 40% as a “current best guess” for Apophis. Applying these parameters to Apophis yields a mass estimate of 2×¹⁰¹⁰ kg with a corresponding energy estimate of 375 Mt for its potential hazard. Substantial unknowns, most notably the total porosity, allow uncertainties in these mass and energy estimates to be as large as factors of two or three.     

The study of instabilities in the solar wind and magnetosheath and their interaction with the Earth's magnetosphere

The thesis concentrates on an analysis of the experimental data as well as numerical simulation of propagation of fast forward (FF) shocks in the solar wind and their evolution through the magnetosheath to the inner magnetosphere. The thesis was defended at the Charles University, Prague, Faculty of Mathematics and Physics, Department of Plasma and Surface Science (V Holesovickach 2, 180 00 Prague 8, Czech Republic) on September 30, 2008 under supervision of Doc. Lubomír P?ech. The thesis is written in English and a resume can be found at http://physics.mff.cuni.cz/kfpp/phd/andreeova.pdf.     

A comparison of local simulations and reduced models of MRI-induced turbulence

We run mean-field shearing-box numerical simulations with a temperature-dependent resistivity and compare them to a reduced dynamical model. Our simulations reveal the co-existence of two quasi-steady states, a 'quiet' state and an 'active' turbulent state, confirming the predictions of the reduced model. The initial conditions determine on which state the simulation ultimately settles. The active state is strongly influenced by the geometry of the computational box and the thermal properties of the gas. Cubic domains support permanent channel flows, bar-shaped domains exhibit eruptive behaviour, and horizontal slabs give rise to infrequent channels. Meanwhile, longer cooling time-scales lead to higher saturation amplitudes.     

Water sorption on martian regolith analogs: Thermodynamics and near-infrared reflectance spectroscopy

The near-infrared reflectance spectra of the martian surface present strong absorption features attributed to hydration water present in the regolith. In order to characterize the relationships between this water and atmospheric vapor and decipher the physical state of water molecules in martian regolith analogs, we designed and built an experimental setup to measure near-IR reflectance spectra under martian atmospheric conditions. Six samples were studied that cover part of the diversity of Mars surface mineralogy: a hydrated ferric oxide (ferrihydrite), two igneous samples (volcanic tuff, and dunite sand), and three potential water rich soil materials (Mg-sulfate, smectite powder and a palagonitic soil, the JSC Mars-1 regolith stimulant). Sorption and desorption isotherms were measured at 243 K for water vapor pressure varying from 10⁻⁵ to ∼0.3 mbar (relative humidity: 10⁻⁴ to 75%). These measurements reveal a large diversity of behavior among the sample suite in terms of absolute amount of water adsorbed, shape of the isotherm and hysteresis between the adsorption and desorption branches. Simultaneous in situ spectroscopic observations permit a detailed analysis of the spectral signature of adsorbed water and also point to clear differences between the samples. Ferric (oxy)hydroxides like ferrihydrite or other phases present in palagonitic soils are very strong water adsorbent and may play an important role in the current martian water cycle by allowing large exchange of water between dust-covered regions and atmosphere at diurnal and seasonal scales.     

Melting and Sublimation of Planetary Ices Under Low Pressure Conditions: Laboratory Experiments with a Melting Probe Prototype

One possibility to explore the subsurface layers of icy bodies is to use a probe with a “hot tip", which is able to penetrate ice layers by melting. Such probes have been built and used in the past for the exploration of terrestrial polar ice sheets and may also become useful tools to explore other icy layers in the Solar System. Examples for such layers are the polar areas of Mars or the icy crust of Jupiter’s moon Europa. However, while on Earth a heated probe launched into an ice sheet always causes melting with subsequent refreezing, the behaviour of such a probe in a low pressure environment is quite different. We report on the results of some experiments with a simple “melting probe" prototype with two different kinds of hot tips in a vacuum environment. For one of the tips the probe moved into two types of ice samples: (i) compact water ice and (ii) porous water ice with a snow (firn) like texture. It was also found that the penetration behaviour was basically different for the two sample types even when the same kind of tip was used. While in the porous sample the ice was only subliming, the phase changes occurring during the interaction of the tip with the compact ice are much more complex. Here alternating phases of melting and sublimation occur. The absence of the liquid phase has severe consequences on the performance of a “melting probe" under vacuum conditions: In this environment we find a high thermal resistance between the probe surface and the underlying ice. Therefore, only a low percentage of the heat that is generated in the tip is used to melt or sublime the ice, the bulk of the power is transferred towards the rear end of the probe. This is particularly a problem in the initial phases of an ice penetration experiment, when the probe has not yet penetrated the ice over its whole length. In the compact ice sample, phases could be observed, where a high enough gas pressure had built up locally underneath the probe, so that melting becomes possible. Only during these melting periods the thermal contact between the probe and the ice is good and in consequence the melting probe works effectively.     

The South America VLF NETwork (SAVNET)

In this paper we present the South America VLF NETwork (SAVNET), a new observing facility at very low frequencies. It has been recently installed at different locations spread over Latin America, in Brazil, Peru and Argentina. It consists of a network of seven Very Low Frequency (VLF) receivers with the main scientific objective of monitoring the solar activity on short (minutes to hours) and long (years) time scales. Other objectives include a better understanding of the spatial structure of the South Atlantic Magnetic Anomaly, the study of atmospheric phenomena and the search for genuine seismic-electromagnetic effects. After discussing the scientific goals, the details of the installation are presented as well as the first results recently obtained.     

Solubility of Pt in sulphide mattes: Implications for the genesis of PGE-rich horizons in layered intrusions

The partitioning of Pt in sulphide melt (matte) has been studied as a function of fS₂ and fO₂ at 1200 and 1300 °C. The results show that the solubility of Pt in mattes increases strongly with increasing fS₂ and decreases weakly with increasing fO₂. The increase in Pt solubility with increasing fS₂ is attributed to Pt dissolving in the melt as a sulphide species and the weak inverse dependence of Pt solubility on fO₂ to the diluting effect of increasing O in the melt at high fO₂. These results, coupled with measurements of Pt solubility in silicate melts taken from the literature, allow the calculation of Pt matte/silicate-melt partition coefficients () for a range of conditions pertinent to the formation of Pt-rich horizons in layered intrusions. The calculated values range between 10⁷ and 10¹¹, depending on fO₂ and fS₂, several orders of magnitude higher than previously published values. Our preferred value for for conditions appropriate to the Merensky Reef is 10⁷ and for the Stillwater Pt-rich horizon 10⁸. The new results are consistent with the magmatic hypothesis for Pt-rich horizons in layered intrusions.     

Reduced sulfur species in a stratified seawater lake (Rogoznica Lake, Croatia); seasonal variations and argument for organic carriers of reactive sulfur

Over a period of a year, Hg⁰-reactive, total reduced sulfur species (RSS_T), as well as a non-volatile fraction that cannot be gas-stripped at pH ∼2 (RSS_NV), have been measured by voltammetry in a stratified, saline lake. In the hypolimnion, RSS_T is dominated by unusually high (up to 5 mM) dissolved divalent sulfur (S^−II), present as H₂S + HS⁻ and as inorganic polysulfides (H_xS_n^x−2). Less abundant RSS_NV is attributed to dissolved zero-valent sulfur (S⁰) in inorganic polysulfides. Assuming negligible contribution of organic S⁰ species in the hypolimnion, the equilibrium distribution of polysulfide ions is calculated; S₅²⁻ is found to predominate. In the epilimnion, all RSS_T consists of RSS_NV within analytical uncertainty. Through spring and summer, RSS_T and RSS_NV display little vertical or seasonal variation, but they increase dramatically when stratification breaks down in autumn. Based on decay rate, RSS during mixing events is attributed to dissolved S₈ from oxidation of sulfide and decomposition of inorganic polysulfides. This hypothesis quantitatively predicts precipitation of elemental sulfur in a year when colloidal sulfur was observed and predicts no precipitation in a year when it was not observed. Except during mixing events, the entire water column is undersaturated with respect to both rhombic sulfur and biologic sulfur, and the limited variations of RSS exclude hydrophobic and volatile aqueous S₈ as a major species. During such periods, RSS (typically 8 nM) may be associated with organic carbon, perhaps as adsorbed S₈ or as covalently bound polysulfanes or polysulfides. The hypolimnion is viewed as a zero-valent sulfur reactor that creates S⁰-containing, dissolved organic macromolecules during stable stratification periods. Some are sufficiently degradation-resistant and hydrophilic to be dispersed throughout the lake during mixing events, subsequently giving rise to ∼10⁻⁸ M RSS in the oxic water column. Voltammetrically determined RSS in oxic natural waters has often been described as “sulfide” or “metal complexed sulfide”, implying an oxidation state of S^−II; we argue that RSS in oxic Rogoznica Lake waters is mainly S⁰.     

Oxygen isotopes composition of sapphires from the French Massif Central: implications for the origin of gem corundum in basaltic fields

Alluvial and colluvial gem sapphires are common in the basaltic fields of the French Massif Central (FMC) but sapphire-bearing xenoliths are very rare, found only in the Menet trachytic cone in Cantal. The O-isotope composition of the sapphires ranges between 4.4 and 13.9‰. Two distinct groups have been defined: the first with a restricted isotopic range between 4.4 and 6.8‰ (n = 22; mean δ¹⁸O = 5.6 ± 0.7‰), falls within the worldwide range defined for blue-green-yellow sapphires related to basaltic gem fields (3.0 < δ¹⁸O < 8.2‰, n = 150), and overlaps the ranges defined for magmatic sapphires in syenite (4.4 < δ¹⁸O < 8.3‰, n = 29). A second group, with an isotopic range between 7.6 and 13.9‰ (n = 9), suggests a metamorphic sapphire source such as biotite schist in gneisses or skarns. The δ¹⁸O values of 4.4–4.5‰ for the blue sapphire-bearing anorthoclasite xenolith from Menet is lower than the δ¹⁸O values obtained for anorthoclase (7.7–7.9‰), but suggest that these sapphires were derived from an igneous reservoir in the subcontinental spinel lherzolitic mantle of the FMC. The presence of inclusions of columbite-group minerals, pyrochlore, Nb-bearing rutile, and thorite in these sapphires provides an additional argument for a magmatic origin. In the FMC lithospheric mantle, felsic melts crystallized to form anorthoclasites, the most evolved peraluminous variant of the alkaline basaltic melt. The O-isotopic compositions of the first group suggests that these sapphires crystallized from felsic magmas under upper mantle conditions. The second group of isotopic values, typified for example by the Le Bras sapphire with a δ¹⁸O of 13.9‰, indicates that metamorphic sapphires from granulites were transported to the surface by basaltic magma.