Heavily‐hydrated lithic clasts in CH chondrites and the related,metal‐rich chondrites Queen Alexandra Range 94411 and Hammadah al Hamra 237

Abstract— Fine‐grained, heavily‐hydrated lithic clasts in the metal‐rich (CB) chondrites Queen Alexandra Range (QUE) 94411 and Hammadah al Hamra 237 and CH chondrites, such as Patuxent Range (PAT) 91546 and Allan Hills (ALH) 85085, are mineralogically similar suggesting genetic relationship between these meteorites. These clasts contain no anhydrous silicates and consist of framboidal and platelet magnetite, prismatic sulfides (pentlandite and pyrrhotite), and Fe‐Mn‐Mg‐bearing Ca‐carbonates set in a phyllosilicate‐rich matrix. Two types of phyllosilicates were identified: serpentine, with basal spacing of ?0.73 nm, and saponite, with basal spacings of about 1.1–1.2 nm. Chondrules and FeNi‐metal grains in CB and CH chondrites are believed to have formed at high temperature (>1300 K) by condensation in a solar nebula region that experienced complete vaporization. The absence of aqueous alteration of chondrules and metal grains in CB and CH chondrites indicates that the clasts experienced hydration in an asteroidal setting prior to incorporation into the CH and CB parent bodies. The hydrated clasts were either incorporated during regolith gardening or accreted together with chondrules and FeNi‐metal grains after these high‐temperature components had been transported from their hot formation region to a much colder region of the solar nebula.     

Simulations of baryon oscillations

The coupling of photons and baryons by Thomson scattering in the early universe imprints features in both the cosmic microwave background (CMB) and matter power spectra. The former have been used to constrain a host of cosmological parameters, the latter have the potential to strongly constrain the expansion history of the universe and dark energy. Key to this program is the means to localize the primordial features in observations of galaxy spectra which necessarily involve galaxy bias, non-linear evolution and redshift space distortions. We present calculations, based on mock catalogs produced from high-resolution N-body simulations, which show the range of behaviors we might expect of galaxies in the real universe. We investigate physically motivated fitting forms which include the effects of non-linearity, galaxy bias and redshift space distortions and discuss methods for analysis of upcoming data. In agreement with earlier work, we find that a survey of several Gpc³ would constrain the sound horizon at z  1 to about 1%.     

Experimental determination of photostability and fluorescence‐based detection of PAHs on the Martian surface

Abstract– Even in the absence of any biosphere on Mars, organic molecules, including polycyclic aromatic hydrocarbons (PAHs), are expected on its surface due to delivery by comets and meteorites of extraterrestrial organics synthesized by astrochemistry, or perhaps in situ synthesis in ancient prebiotic chemistry. Any organic compounds exposed to the unfiltered solar ultraviolet spectrum or oxidizing surface conditions would have been readily destroyed, but discoverable caches of Martian organics may remain shielded in the subsurface or within surface rocks. We have studied the stability of three representative polycyclic aromatic hydrocarbons (PAHs) in a Mars chamber, emulating the ultraviolet spectrum of unfiltered sunlight under temperature and pressure conditions of the Martian surface. Fluorescence spectroscopy is used as a sensitive indicator of remaining PAH concentration for laboratory quantification of molecular degradation rates once exposed on the Martian surface. Fluorescence‐based instrumentation has also been proposed as an effective surveying method for prebiotic organics on the Martian surface. We find the representative PAHs, anthracene, pyrene, and perylene, to have persistence half‐lives once exposed on the Martian surface of between 25 and 60 h of noontime summer UV irradiation, as measured by fluorescence at their peak excitation wavelength. This equates to between 4 and 9.6 sols when the diurnal cycle of UV light intensity on the Martian surface is taken into account, giving a substantial window of opportunity for detection of organic fluorescence before photodegradation. This study thus supports the use of fluorescence‐based instrumentation for surveying recently exposed material (such as from cores or drill tailings) for native Martian organic molecules in rover missions.     

The organic composition of C/2001 A2 (LINEAR): II. Search for heterogeneity within a comet nucleus

The nucleus of Comet C/2001 A2 (LINEAR) split several times during its recent apparition, presenting an unusual opportunity to search for chemical differences in freshly exposed material. We conducted this search using NIRSPEC at the W.M. Keck Observatory on four dates in 2001: 9.5 and 10.5 July and 4.4 and 10.5 August. We detected the R0 and R1 lines of the ν₃ vibrational band of CH₄ near 3.3 μm on all dates. The R2 line was detected on 4.4 and 10.5 August. When we compare production rates of CH₄ to H₂O, we find evidence of a significant enhancement in August relative to that found in July. H₂CO was securely detected via its ν₁ and ν₅ bands on 9.5 July. On 10.5 July, H₂CO emission was much weaker, and its mixing ratio had dropped by a factor of about four. The mixing ratios for other detected volatile species did not change significantly over the course of the observations. We discuss the implications of this evidence for chemical heterogeneity in the nucleus of Comet C/2001 A2.     

Altered basaltic glass: A terrestrial analog to the soil of Mars

Analyses of Martian surface soil by Viking and Earth-based telescopes have been interpreted as indicating a regolith dominated by the weathering products of mafic or ultramafic rocks. Basaltic glass has previously been proposed as a more likely precursor than crystalline rock, given the low efficiency of surface weathering under present Martian conditions. On Earth large volumes of basaltic glass formed by quenching of magma by water. A similar interaction, between magma and ground ice, may have been a common occurrence on Mars. On the basis of this scenario palagonite, the alteration product of basaltic sideromelane glass, was studied as a possible analog to Martian soil. Samples from Iceland, Alaska, Antarctica, Hawaii, and the desert of New Mexico and Mexico were examined by optical and scanning electron microscopy, electron microprobe analysis, X-ray diffraction, spectrophotometry, and magnetic and thermogravimetric analysis. We suggest that palagonite is a good analog to the surface soil of Mars in chemical composition, particle size, spectral signature, and magnetic properties. Our model for the formation of fine-grained Martian surface soil begins with eruptions of basaltic magma through ground ice, forming deposits of glassy tuff. Individual glass shards are then altered by low-temperature hydrothermal systems to palagonitic material. Dehydration and aeolian abrasion strip the alteration rinds from the glass, and wind storms distribute the silt-sized palagonitic fragments in a planet-wide deposit.     

Analysis of Cassini/CIRS limb spectra of Titan acquired during the nominal mission II: Aerosol extinction profiles in the 600–1420 cm spectral range

We have analyzed the continuum emission of limb spectra acquired by the Cassini/CIRS infrared spectrometer in order to derive information on haze extinction in the 3–0.02 mbar range (∼150–350 km). We focused on the 600–1420 cm⁻¹ spectral range and studied nine different limb observations acquired during the Cassini nominal mission at 55°S, 20°S, 5°N, 30°N, 40°N, 45°N, 55°N, 70°N and 80°N. By means of an inversion algorithm solving the radiative transfer equation, we derived the vertical profiles of haze extinction coefficients from 17 spectral ranges of 20-cm⁻¹ wide at each of the nine latitudes. At a given latitude, all extinction vertical profiles retrieved from various spectral intervals between 600 and 1120 cm⁻¹ display similar vertical slopes implying similar spectral characteristics of the material at all altitudes. We calculated a mean vertical extinction profile for each latitude and derived the ratio of the haze scale height (H_haze) to the pressure scale height (H_gas) as a function of altitude. We inferred H_haze/H_gas values varying from 0.8 to 2.4. The aerosol scale height varies with altitude and also with latitude. Overall, the haze extinction does not show strong latitudinal variations but, at 1 mbar, an increase by a factor of 1.5 is observed at the north pole compared to high southern latitudes. The vertical optical depths at 0.5 and 1.7 mbar increase from 55°S to 5°N, remain constant between 5°N and 30°N and display little variation at higher latitudes, except the presence of a slight local maximum at 45°N. The spectral dependence of the haze vertical optical depth is uniform with latitude and displays three main spectral features centered at 630 cm⁻¹, 745 cm⁻¹ and 1390 cm⁻¹, the latter showing a wide tail extending down to ∼1000 cm⁻¹. From 600 to 750 cm⁻¹, the optical depth increases by a factor of 3 in contrast with the absorbance of laboratory tholins, which is generally constant. We derived the mass mixing ratio profiles of haze at the nine latitudes. Below the 0.4-mbar level all mass mixing ratio profiles increase with height. Above this pressure level, the profiles at 40°N, 45°N, 55°N, at the edge of the polar vortex, display a decrease-with-height whereas the other profiles increase. The global increase with height of the haze mass mixing ratio suggest a source at high altitudes and a sink at low altitudes. An enrichment of haze is observed at 0.1 mbar around the equator, which could be due to a more efficient photochemistry because of the strongest insolation there or an accumulation of haze due to a balance between sedimentation and upward vertical drag.