Raman spectroscopic properties and Raman identification of CaS‐MgS‐MnS‐FeS‐Cr2FeS4 sulfides in meteorites and reduced sulfur‐rich systems

Raman spectra were acquired on a series of natural and synthetic sulfide minerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite ((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr₂FeS₄). Natural samples come from three enstatite chondrites, three aubrites, and one anomalous ungrouped enstatite meteorite. Synthetic samples range from pure endmembers (CaS, FeS, MgS) to complex solid solutions (Fe, Mg, Ca)S. The main Raman peaks are localized at 225, 285, 360, and 470 cm^?1 for the Mg‐rich sulfides; at 185, 205, and 285 cm^?1 for the Ca‐rich sulfides; at 250, 370, and 580 cm^?1 for the Mn‐rich sulfides; at 255, 290, and 365 cm^?1 for the Cr‐rich sulfides; and at 290 and 335 cm^?1 for troilite with, occasionally, an extra peak at 240 cm^?1. A peak at 160 cm^?1 is present in all Raman spectra and cannot be used to discriminate between the different sulfide compositions. According to group theory, none of the cubic monosulfides oldhamite, niningerite, or alabandite should present first‐order Raman spectra because of their ideal rocksalt structure. The occurrence of broad Raman peaks is tentatively explained by local breaking of symmetry rules. Measurements compare well with the infrared frequencies calculated from first‐principles calculations. Raman spectra arise from activation of certain vibrational modes due to clustering in the solid solutions or to coupling with electronic transitions in semiconductor sulfides.     

A comparative study of opaque phases in Qingzhen (EH3) and MacAlpine Hills 88136 (EL3): Representatives of EH and EL parent bodies

Abstract— Opaque minerals in the Qingzhen (EH3) and MacAlpine Hills (MAC) 88136 (EL3) enstatite chondrites were studied and compared with other EH and EL chondrites. All opaque minerals usually occur in multi‐sulfide‐metal clasts and nodules in the matrix between chondrules (El Goresy et al., 1988). The higher abundance of opaque minerals, the occurrence of niningerite and various alkali‐sulfides (e.g., caswellsilverite, phases A and B, djerfisherite) are diagnostic criteria for EH chondrites, while alabandite is characteristic for EL chondrites. In addition, EH chondrites are characterized by enrichments of Si in both kamacite and perryite, and alkali elements in sphalerite and chalcopyrite. The Mn contents of daubreelite and sphalerite are lower in EH than in EL chondrites. These are consistent with lower oxygen fugacity and higher H₂S fugacity of EH than EL chondrites. In contrast, the discovery of sphalerite and Zn‐rich daubreelite in MAC 88136 indicates that their absence in EL6 chondrites is probably related to thermal metamorphism in the parent body. Schreibersite microspherules are commonly enclosed in most sulfides in Qingzhen, but are absent in MAC 88136. They were once molten, and probably predated all sulfide host phases. The petrographic setting and chemical compositions of the sulfide hosts of the schreibersite microspherules in EH3 chondrites are consistent with formation by condensation. The earliest sulfide condensates oldhamite and niningerite occupy the interiors of the clasts and nodules, whereas the rims consist of troilite and djerfisherite. In addition, in Qingzhen, some other troilite, djerfisherite and sphalerite assemblages coexist with perryite. They were produced by sulfurization of metallic Fe‐Ni in the nebula. In MAC 88136, sulfurization of Si‐bearing Fe‐Ni metal is less pronounced, and it produced troilite, schreibersite and less abundant perryite. Two kinds of normal zoning and a reverse zoning trends of niningerite, and both normal and reverse zoning of sphalerite were found in clasts and nodules in Qingzhen. The coexistence of normal and reverse zoning profiles in niningerite grains in the same meteorite strongly suggests that they formed before accretion in the parent body, because an asteroidal metamorphic or an impact event in the parent body would have erased these contrasting profiles and destroyed the textural settings. In contrast, alabandite in MAC 88136 shows only normal zoning, with the FeS content decreasing to 9.3 mol% toward troilite, indicating very slow cooling at low temperature.     

On the significance of diopside and oldhamite in enstatite chondrites and aubrites

Abstract— Enstatite is the primary silicate phase of equilibrated enstatite chondrites (EECs). The CaO contents of these enstatites lie close to or on the enstatite-diopside phase boundary, yet, curiously, diopside has always been absent from EEC assemblages. In contrast, aubrites contain abundant diopside even though they are thought to be derived from an E chondrite-like protolith. A phase equilibrium analysis of the Ca-Mg-Fe-Mn-Si-O-S system under reducing conditions solves this enigma and shows that diopside-bearing EECs should commonly be found. When S fugacity is sufficiently high (e.g., Fe-FeS buffer), low O fugacity limits the stability of diopside in favor of oldhamite. Under such conditions, the relative stability of diopside and oldhamite is described by the reaction: CaMgSi₂O₆ + MgS = CaS + Mg₂Si₂O₆ A large bulk compositional field exists where diopside and oldhamite are simultaneously stable. The existence of oldhamite does not preclude the stability of diopside. Phase diagram topology demonstrates that bulk compositions lying in the enstatite-oldhamite field and enstatite-oldhamite-alabandite field have enstatite CaO contents nearly identical to that of enstatite in equilibrium with diopside alone. This explains the high enstatite CaO contents of all EECs that do not contain diopside. This study also reports the discovery of the first EEC to contain metamorphic diopside, the Antarctic meteorite EET 90102. Elephant Moraine 90102 has a typical EL6 texture and contains the assemblage: enstatite, diopside, albite, kamacite, troilite, sinoite, and graphite. Trace quantities of alabandite, oldhamite and daubreelite are also present. Diopside is stable in EET 90102 because its bulk composition lies within either the enstatite-diopside-oldhamite-alabandite or diopside-alabandite-enstatite stability fields. In contrast, all other EECs analyzed to date have bulk compositions lying in the enstatite-oldhamite-alabandite stability field. The discovery of diopside in EET 90102 helps confirm the predictions of the phase equilibrium analysis. Elephant Moraine 90102 experienced a high-temperature metamorphic equilibration from which it was quenched. The enstatite-diopside, CaS in alabandite and Fe in alabandite, geothermometers yield temperatures of last equilibration of ～900 °C. The absence of daubreelite and schreibersite along with high troilite Cr contents and high kamacite P contents confirm a high-temperature metamorphic quench. The EET 90102 chondrite experienced a somewhat different cooling history and has a slightly different bulk composition than all other EECs studied to date; however, the close mineralogic, petrologic and textural similarities between EET 90102 and nominal EL6 chondrites signify that it should be classified as a diopside- and sinoite-bearing EL6 chondrite. Assuming that the aubrites formed from an E chondrite-like protolith, a source rock similar to that of a diopside-bearing EEC offers a clear advantage for aubrite formation. Melting of a diopside-saturated EEC protolith would not require conversion of CaS to achieve diopside-saturation upon cooling.     

Metal‐saturated sulfide assemblages in NWA 2737: Evidence for impact‐related sulfur devolatilization in Martian meteorites

NWA 2737, a Martian meteorite from the Chassignite subclass, contains minute amounts (0.010 ± 0.005 vol%) of metal‐saturated Fe‐Ni sulfides. These latter bear evidence of the strong shock effects documented by abundant Fe nanoparticles and planar defects in Northwest Africa (NWA) 2737 olivine. A Ni‐poor troilite (Fe/S = 1.0 ± 0.01), sometimes Cr‐bearing (up to 1 wt%), coexists with micrometer‐sized taenite/tetrataenite‐type native Ni‐Fe alloys (Ni/Fe = 1) and Fe‐Os‐Ir‐(Ru) alloys a few hundreds of nanometers across. The troilite has exsolved flame‐like pentlandite (Fe/Fe + Ni = 0.5–0.6). Chalcopyrite is almost lacking, and no pyrite has been found. As a hot desert find, NWA 2737 shows astonishingly fresh sulfides. The composition of troilite coexisting with Ni‐Fe alloys is completely at odds with Chassigny and Nahkla sulfides (pyrite + metal‐deficient monoclinic‐type pyrrhotite). It indicates strongly reducing crystallization conditions (close to IW), several log units below the fO₂ conditions inferred from chromites compositions and accepted for Chassignites (FMQ‐1 log unit). It is proposed that reduction in sulfides into base and precious metal alloys is operated via sulfur degassing, which is supported by the highly resorbed and denticulated shape of sulfide blebs and their spongy textures. Shock‐related S degassing may be responsible for considerable damages in magmatic sulfide structures and sulfide assemblages, with concomitant loss of magnetic properties as documented in some other Martian meteorites.     

Solar activity variations of thermospheric temperatures on Mars and a problem of CO in the lower atmosphere

Long-term MGS drag density observations at 390 km reveal variations of the density with season L_S (by a factor of 2) and solar activity index F_10.7 (by a factor of 3 for F_10.7 = 40-100). According to Forbes et al. (Forbes, J.M., Lemoine, F.G., Bruinsma, S.L., Smith, M.D., Zhang, X. [2008]. Geophys. Res. Lett. 35, L01201, doi:10.1029/2007GL031904), the variation with F_10.7 reflects variations of the exospheric temperature from 192 to 284 K. However, the derived temperature range corresponds to variation of the density at 390 km by a factor of 8, far above the observed factor of 3. The recent thermospheric GCMs agree with the derived temperatures but do not prove their adequacy to the MGS densities at 390 km. A model used by Forbes et al. neglects effects of eddy diffusion, chemistry and escape on species densities above 138 km. We have made a 1D-model of neutral and ion composition at 80-400 km that treats selfconsistently chemistry and transport of species with F_10.7, T_∞, and [CO₂]_80 km as input parameters. Applying this model to the MGS densities at 390 km, we find variation of T_∞ from 240 to 280 K for F_10.7 = 40 and 100, respectively. The results are compared with other observations and models. Temperatures from some observations and the latest models disagree with the MGS densities at low and mean solar activity. Linear fits to the exospheric temperatures are T_∞ = 122 + 2.17F_10.7 for the observations, T_∞ = 131 + 1.46F_10.7 for the latest models, and T_∞ = 233 + 0.54F_10.7 for the MGS densities at 390 km. Maybe the observed MGS densities are overestimated near solar minimum when they are low and difficult to measure. Seasonal variations of Mars’ thermosphere corrected for the varying heliocentric distance are mostly due to the density variations in the lower and middle atmosphere and weakly affect thermospheric temperature. Nonthermal escape processes for H, D, H₂, HD, and He are calculated for the solar minimum and maximum conditions.Another problem considered here refers to Mars global photochemistry in the lower and middle atmosphere. The models gave too low abundances of CO, smaller by an order of magnitude than those observed. Our current work shows that modifications in the boundary conditions proposed by Zahnle et al. (Zahnle, K., Haberle, R.M., Catling, D.C., Kasting, J.F. [2008]. J. Geophys. Res. 113, E11004, doi:10.1029/2008JE003160) are reasonable but do not help to solve the problem.     

Mechanistic studies on the decomposition of carbon suboxide in a cometary ice analog

A cometary ice analog sample consisting primarily of carbon suboxide ice (C₃O₂) was produced from the irradiation of its precursor, carbon monoxide. This carbon suboxide sample was subjected to irradiation with energetic electrons at 10 K to simulate the interaction of carbon suboxide-rich cometary analog ices with ionizing radiation. The destruction of carbon suboxide as well as the production of the primary degradation products, dicarbon monoxide (C₂O), and carbon monoxide (CO), were monitored quantitatively by infrared spectroscopy in situ; the gas phase was simultaneously sampled via quadrupole mass spectrometry. A kinetic model was produced to help explain the decomposition kinetics of carbon suboxide in cometary ices and to infer the underlying reaction mechanisms.     

Flowing afterglow studies of temperature dependencies for electron dissociative recombination of HCNH, CH3CNH and CH3CH2CNH and their symmetrical proton-bound dimers

A study has been made using a variable temperature flowing afterglow Langmuir probe technique (VT-FALP) to determine the equilibrium temperature dependencies of the dissociative electron-ion recombination of the protonated cyanide ions (RCNH⁺, where R=H, CH₃ and C₂H₅) and their symmetrical proton-bound dimers (RCNH⁺NCR). The power law temperature dependencies of the recombination coefficients, α_e, over the temperature range 180 to 600 K for the protonated ions are α_e(T)(cm³ s⁻¹)=3.5±0.5×10⁻⁷ (300/T)^1.38 for HCNH⁺, α_e(T)=3.4±0.5×10⁻⁷ (300/T)^1.03 for CH₃CNH⁺, and α_e(T)=4.6±0.7×10⁻⁷ (300/T)^0.81 for CH₃CH₂CNH⁺. The equivalent values for the proton-bound dimers are α_e(T)(cm³ s⁻¹)=2.4±0.4×10⁻⁶(300/T)^0.5 for (HCN)₂H⁺ to α_e(T)=2.8±0.4×10⁻⁶(300/T)^0.5 for (CH₃CN)₂H⁺, and α_e(T)=2.3±0.3×10⁻⁶(300/T)^0.5 for (CH₃CH₂CN)₂H⁺. The relevance of these data to molecular synthesis in the interstellar medium and the Titan ionosphere are discussed.     

Impact-induced N2 production from ammonium sulfate: Implications for the origin and evolution of N2 in Titan’s atmosphere

Chemical reactions and volatile supply through hypervelocity impacts may have played a key role for the origin and evolution of both planetary and satellite atmospheres. In this study, we evaluate the role of impact-induced N₂ production from reduced nitrogen-bearing solids proposed to be contained in Titan’s crust, ammonium sulfate ((NH₄)₂SO₄), for the replenishment of N₂ to the atmosphere in Titan’s history. To investigate the conversion of (NH₄)₂SO₄ into N₂ by hypervelocity impacts, we measured gases released from (NH₄)₂SO₄ that was exposed to hypervelocity impacts created by a laser gun. The sensitivity and accuracy of the measurements were enhanced by using an isotope labeling technique for the target. We obtained the efficiency of N₂ production from (NH₄)₂SO₄ as a function of peak shock pressure ranging from ∼8 to ∼45 GPa. Our results indicate that the initial and complete shock pressures for N₂ degassing from (NH₄)₂SO₄ are ∼10 and ∼25 GPa, respectively. These results suggest that cometary impacts on Titan (i.e., impact velocity v_i > ∼8 km/s) produce N₂ efficiently; whereas satellitesimal impacts during the accretion (i.e., v_i < 4 km/s) produce N₂ only inefficiently. Even when using the proposed small amount of (NH₄)₂SO₄ content in the crust (∼4 wt.%) (Fortes, A.D. et al., 2007. Icarus 188, 139-153), the total amount of N₂ provided through cometary impacts over 4.5 Ga reaches ∼2-6 times the present atmospheric N₂ (i.e., ∼7 × 10²⁰-2 × 10²¹ [mol]) based on the measured production efficiency and results of a hydrodynamic simulation of cometary impacts onto Titan. This implies that cometary impacts onto Titan’s crust have the potential to account for a large part of the present N₂ through the atmospheric replenishment after the accretion.     

The Umov effect for single irregularly shaped particles with sizes comparable with wavelength

The Umov effect manifests itself as an inverse correlation between the linear polarization maximum of an object’s scattered light P_max and its geometric albedo A. This effect is observed for the Moon, Mercury and Mars, and there are data suggesting this effect is valid for asteroids. The Umov effect is due to the contribution of interparticle multiple scattering that increases albedo and decreases polarization. We here study if the Umov effect can be extended to the case of single irregularly shaped particles with sizes comparable with the wavelength. This, in particular, is important for cometary dust polarimetry. We show the Umov effect being valid for weakly absorbing irregular particles (Im(m) ? 0.02) almost through the entire range of size parameters x considered. Highly absorbing particles (Im(m) > 0.02) follow the Umov effect only if x exceeds 14. In the case of weakly absorbing particles, the inverse correlation is essentially non-linear, which is caused by the contribution of particles with small x. However, averaging over many different types of irregularly shaped particles could make it significantly more linear. The size averaging does not change qualitatively the diagram log(P_max)-log(A) for weakly absorbing particles. For single irregular particles whose sizes are comparable with wavelength, there is no reliable correlation between the slope of the polarization curve h near the inversion phase angle and geometric albedo A. Using the extended Umov Law, we estimate the geometric albedo of dust particles forming cometary circumnuclear haloes A = 0.1 − 0.2, which is a few times larger than the average geometric albedo over the entire comae. Note that, using the obtained values for A of cometary particles, one can derive their number density in circumnuclear haloes from photometric observations.     

New findings for the equilibrated enstatite chondrite Grein 002

Abstract— We report new petrographic and chemical data for the equilibrated EL chondrite Grein 002, including the occurrence of osbornite, metallic copper, abundant taenite, and abundant diopside. As inferred from low Si concentrations in kamacite, the presence of ferroan alabandite, textural deformation, chemical equilibration of mafic silicates, and a subsolar noble gas component, we concur with Grein 002's previous classification as an EL4‐5 chondrite. Furthermore, the existence of pockets consisting of relatively coarse, euhedral enstatite crystals protruding large patches of Fe‐Ni alloys suggests to us that this EL4‐5 chondrite has been locally melted. We suspect impact induced shock to have triggered the formation of the melt pockets. Mineralogical evidence indicates that the localized melting of metal and adjacent enstatite must have happened relatively late in the meteorite's history. The deformation of chondrules, equilibration of mafic silicates, and generation of normal zoning in Fe, Zn‐sulfides took place during thermal alteration before the melting event. Following parent body metamorphism, daubreelite was exsolved from troilite in response to a period of slow cooling at subsolidus temperatures. Exsolution of schreibersite from the coarse metal patches probably occurred during a similar period of slow cooling subsequent to the event that induced the formation of the melt pockets. Overall shock features other than localized melting correspond to stage S2 and were likely established by the final impact that excavated the Grein 002 meteoroid.     

The thermal and physical characteristics of the Gao-Guenie (H5) meteorite

Measurements of the bulk density, grain density, porosity, and magnetic susceptibility of 19 Gao-Guenie H5 chondrite meteorite samples are presented. We find average values of bulk density 〈ρ_bulk〉=3.46±0.07 g/cm³, grain density 〈ρ_grain〉=3.53±0.08 g/cm³, porosity 〈P(%)〉=2.46±1.39, and bulk mass magnetic susceptibility 〈log χ〉=5.23±0.11. Measurements of the specific heat capacity for a 3.01-g Gao-Guenie sample, a 61.37-g Gao-Guenie sample, a 62.35-g Jilin H5 chondrite meteorite sample, and a 51.37-g Sikhote-Alin IIAB Iron meteorite sample are also presented. Temperature interpolation formula are further provided for the specific heat capacity, thermal conductivity, and thermal diffusivity of the 3.01-g Gao-Guenie sample in the temperature range 300<T (K)<800. We briefly review the possible effects of the newly deduced specific heat and thermal conductivity values on the ablation of meteoroids within the Earth's atmosphere, the modeling of asteroid interiors and the orbital evolution of meteoroids through the Yarkovsky-O’Keefe-Radzievskii-Paddack (YORP) effect.     

Mineralogy and crystallization history of the Ilafegh 009 EL-chondritic impact melt rock: An ATEM investigation

Abstract— The Ilafegh 009 meteorite is an impact melt rock from an EL-chondritic parent body. Its mineralogic assemblage is the result of rapid crystallization after shock-induced melting. We report here an analytical transmission electron microscopy (ATEM) study of the major minerals of this meteorite (enstatite, plagioclase, Fe-Ni metal and sulfides). Based on this study, we discuss the crystallization sequence and the further evolution of the rock in the solid state. Microstructure and microanalyses confirm that the mineralogy of Ilafegh 009 results from the crystallization of an EL-chondritic melt. The high compositional variability of plagioclases and the presence of silica-rich glass pockets indicate fast cooling. During crystallization, the large enstatite grains trapped a large number of phases (plagioclase, silica-rich glass and enstatite nuclei). Sulfides (troilite, alabandite and daubreelite) form finely polycrystalline areas and reveal a complex crystallization sequence. Although Fe-Ni metal grains formed during rapid cooling, their microstructures show that some postsolidification process occurred in Ilafegh 009. A large number of tiny Ni-P-Si-rich precipitates were detected that formed as a result of exsolution of elements that become insoluble in kamacite at low temperature. Finally, the microstructure (dislocation arrangements and phase transformations) observed in enstatite and Fe-Ni metal attests that Ilafegh 009 also experienced a moderate postsolidification shock event.     

A spatially resolved high spectral resolution study of Neptune’s stratosphere

Using TEXES, the Texas Echelon cross Echelle Spectrograph, mounted on the Gemini North 8-m telescope we have mapped the spatial variation of H₂, CH₄, C₂H₂ and C₂H₆ thermal-infrared emission of Neptune. These high-spectral-resolution, spatially resolved, thermal-infrared observations of Neptune offer a unique glimpse into the state of Neptune’s stratosphere in October 2007, L_S = 275.4° just past Neptune’s southern summer solstice (L_S = 270°). We use observations of the S(1) pure rotational line of molecular hydrogen and a portion of the ν₄ band of methane to retrieve detailed information on Neptune’s stratospheric vertical and meridional thermal structure. We find global-average temperatures of 163.8 ± 0.8, 155.0 ± 0.9, and 123.8 ± 0.8 K at the 7.0 × 10⁻³-, 0.12-, and 2.1-mbar levels with no meridional variations within the errors. We then use the inferred temperatures to model the emission of C₂H₂ and C₂H₆ in order to derive stratospheric volume mixing ratios (hence forth, VMR) as a function of pressure and latitude. There is a subtle meridional variation of the C₂H₂ VMR at the 0.5-mbar level with the peak abundance found at −28° latitude, falling off to the north and south. However, the observations are consistent within error to a meridionally constant C₂H₂ VMR of at 0.5 mbar. We find that the VMR of C₂H₆ at 1-mbar peaks at the equator and falls by a factor of 1.6 at −70° latitude. However, a meridionally constant VMR of at the 1-mbar level for C₂H₆ is also statistically consistent with the retrievals. Temperature predictions from a radiative-seasonal climate model of Neptune that assumes the hydrocarbon abundances inferred in this paper are lower than the measured temperatures by 40 K at 7 × 10⁻³ mbar, 30 K at 0.12 mbar and 25 K at 2.1 mbar. The radiative-seasonal model also predicts meridional temperature variations on the order of 10 K from equator to pole, which are not observed. Assuming higher stratospheric CH₄ abundance at the equator relative to the south pole would bring the meridional trends of the inferred temperatures and radiative-seasonal model into closer agreement.We have also retrieved observations of C₂H₄ emission from Neptune’s stratosphere using TEXES on the NASA Infrared Telescope Facility (IRTF) in June 2003, L_S = 266°. Using the observations from the middle of the planet and an average of the middle three latitude temperature profiles from the 2007 observations (9.5° of L_S later, the seasonal equivalent of 9.5 Earth days within Earth’s seasonal cycle), we infer a C₂H₄ VMR of at 1.5 × 10⁻³ mbar, a value that is 3.25 times that predicted by global-average photochemical models.     

Appearance of layered structures in numerical simulations of polydisperse bodies accretion: Application to cometary nuclei

A model for the aggregation of size distribution of cometesimals (Gaussian or power law) into cometary nuclei is developed. Upon disruption induced by collisions, sticking and evolution of the tensile strength and density of the cometesimals by sintering processes are taken into account. The resulting cometary nuclei present specific internal structures that have been quantified to allow the comparison with observational constraints and future in situ observations and cometary nucleus sounding with the CONSERT radar on-board the Rosetta mission. A parameter called the homogeneity exponent, μ, determines different aggregation regimes. Fractal aggregates are formed for μ < 0.4. Radial variations in tensile strength appear for 0.4 < μ < 0.6 and vanish for larger values of μ. The initial size distribution (following a Gaussian or power law) of aggregating cometesimals does not influence strongly these values but can change the extent of corresponding layers. If the layering observed on the surface of some cometary nuclei occurs often and originates from primordial structures, this constrains the velocity distribution of aggregating bodies to follow v∝m^-0.25, while a differential size distribution following a power law with exponent between −2 and −3 should result for large bodies, in agreement with current estimations of the size distributions. Such a layered structure would lead to more cohesive, dense and less porous material located near the center of mass of the nucleus predicting an increase of bulk density of comet nuclei with their erosion state.     

Absolute properties of the neglected eclipsing B-type binary HD 194495

We present the results of the high-resolution spectroscopic observations of the neglected binary system HD 194495 (B3 IV-V+B4 V). A combined analysis of three different photometric data set (Tycho B_T and V_T photometry, H_p-band data of Hipparcos and V-band data of ASAS3 photometry) and radial velocities indicates that the system has an orbital period of 4.90494 ± 0.00005 days and an inclination of 69 ± 1 degrees. This solution yields masses and radii of M₁ = 7.57 ± 0.08 M_⊙ and R₁ = 5.82 ± 0.03 R_⊙ for the primary and M₂ = 5.46 ± 0.09 M_⊙ and R₂ = 3.14 ± 0.08 R_⊙ for the secondary. Based on the position of the two stars plotted on a theoretical H-R diagram, we find that the age of the system is ?28 Myr, according to stellar evolutionary models. The spectroscopic and photometric results are in agreement with those obtained using theoretical predictions.     

Dark energy and the anthropic principle

The Hubble constant is split into two terms H = H₁ + H₂ , where H₁ is a decreasing function due to the Big Bang and the subsequent gravitational interaction that slows the expansion of the Universe and H₂ is an increasing function that corresponds to dark energy which accelerates this expansion. For T = 13.7 Gyr we prove that H₂(T) > 5 m/(yr AU). This is a quite large number and thus the impact of dark energy, which is spread almost everywhere uniformly, should be observable not only on large scales, but also in our Solar system. In particular, we show that Earth, Mars and other planets were closer to the Sun 4.5 Gyr ago. The recession speed ≈5.3 m/yr of the Earth from the Sun seems to be just right for an almost constant influx of solar energy from the origin of life on Earth up to the present over which time the Sun’s luminosity has increased approximately linearly. This presents further support for the Anthropic Principle. Namely, the existence of dark energy guarantees very stable conditions for the development of intelligent life on Earth over a period of 3.5 Gyr.     

A possible YORP effect on C and S Main Belt Asteroids

A rotating frequency analysis in a previous paper, showed that two samples of C and S-type asteroids belonging to the Main Belt, but not to any families, present two different values for the transition diameter to a Maxwellian distribution of the rotation frequency, respectively 48 and 33 km. In this paper, after a more detailed statistical analysis, aiming to verify that the result is physically relevant, we found a better estimate for the transition diameter, respectively D_C = 44 ± 2 km and D_S = 30 ± 1 km. The ratio between these estimated transition diameters, D_C/D_S = 1.5 ± 0.1, can be supported with the help of the YORP (Yarkovsky-O’Keefe-Radzievskii-Paddack) effect, although other physical causes cannot be completely ruled out.In this paper we have derived a simple scaling law for YORP which, taking into account the different average heliocentric distance, the bulk density, the albedo and the asteroid “asymmetry surface factor”, has enabled us to reasonably justify the ratio between the diameters transition of C-type and S-type asteroids. The same scaling law can be used to estimate a new ratio between the bulk densities of S and C asteroids samples (giving ρ_S/ρ_C ≈ 2.9 ± 0.3), and can explain why the asteroids near the transition diameter have about the same absolute magnitude. For C-type asteroids, using the found density ratio and other estimates of S-type density, it is also possible to estimate an average bulk density equal to 0.9 ± 0.1 g cm⁻³, a value compatible with icy composition. The suggested explanation for the difference of the transition diameters is a plausible hypothesis, consistent with the data, but it needs to be studied more in depth with further observations.     

Mineralogy and 57Fe Mössbauer spectroscopy of opaque phases in the Neuschwanstein EL6 chondrite

Abstract— This study presents compositional data and ⁵⁷Fe Mössbauer spectra, taken at 295 K and 85 K, of two fragments of the enstatite (EL6) chondrite Neuschwanstein that fell near the famous Neuschwanstein castle (Bavaria, southern Germany) on April 6, 2002. Main silicate minerals are enstatite (Fs 2) and plagioclase (An 20), the main opaque minerals are kamacite and troilite. Small amounts of oldhamite, daubreelite, and schreibersite have been found. The presented Mössbauer data are the first data gathered for an EL6 chondrite. The dominant parts of each Mössbauer spectrum consist of two six‐line patterns due to the presence of ferromagnetic phases kamacite and troilite. In contrast to other chondrites, peaks of other iron species in the central parts of the spectra are missing due to an extremely low content of Fe‐bearing paramagnetic components. The hyperfine interaction parameters for kamacite are internal magnetic hyperfine field H_hf = 333.2 kOe, isomer shift (relative to a metallic Fe foil) IS = 0.01 mm/s, quadrupole splitting QS = 0 mm/s, line width W = 0.41 mm/s. The data for troilite are H_hf = 305.5 kOe, IS = 0.75 mm/s, QS = ?0.85 mm/s, W = 0.34 mm/s.     

Trapping and dynamical evolution of interplanetary dust particles in Earth’s quasi-satellite resonance

We used numerical simulations to model the orbital evolution of interplanetary dust particles (IDPs) evolving inward past Earth’s orbit under the influence of radiation pressure, Poynting–Robertson light drag (PR drag), solar wind drag, and gravitational perturbations from the planets. A series of β values (where β is the ratio of the force from radiation pressure to that of central gravity) were used ranging from 0.0025 up to 0.02. Assuming a composition consistent with astronomical silicate and a particle density of 2.5 g cm⁻³ these β values correspond to dust particle diameters ranging from 200 μm down to 25 μm. As the dust particle orbits decay past 1 AU between 4% (for β = 0.02, or 25 μm) and 40% (for β = 0.0025, or 200 μm) of the population became trapped in 1:1 co-orbital resonance with Earth. In addition to traditional horseshoe type co-orbitals, we found about a quarter of the co-orbital IDPs became trapped as so-called quasi-satellites. Quasi-satellite IDPs always remain relatively near to Earth (within 0.1–0.3 AU, or 10–30 Hill radii, R_H) and undergo two close-encounters with Earth each year. While resonant perturbations from Earth halt the decay in semi-major axis of quasi-satellite IDPs their orbital eccentricities continue to decrease under the influence of PR drag and solar wind drag, forcing the IDPs onto more Earth-like orbits. This has dramatic consequences for the relative velocity and distance of closest approach between Earth and the quasi-satellite IDPs. After 10⁴–10⁵ years in the quasi-satellite resonance dust particles are typically less than 10R_H from Earth and consistently coming within about 3R_H. In the late stages of evolution, as the dust particles are escaping the 1:1 resonance, quasi-satellite IDPs can have deep close-encounters with Earth significantly below R_H. Removing the effects of Earth’s gravitational acceleration reveals that encounter velocities (i.e., velocities “at infinity”) between quasi-satellite IDPs and Earth during these close-encounters are just a few hundred meters per second or slower, well below the average values of 2–4 km s⁻¹ for non-resonant Earth-crossing IDPs with similar initial orbits. These low encounter velocities lead to a factor of 10–100 increase in Earth’s gravitationally enhanced impact cross-section (σ_grav) for quasi-satellite IDPs compared to similar non-resonant IDPs. The enhancement in σ_grav between quasi-satellite IDPs and cometary Earth-crossing IDPs is even more pronounced, favoring accretion of quasi-satellite dust particles by a factor of 100–3000 over the cometary IDPs. This suggests that quasi-satellite dust particles may dominate the flux of large (25–200 μm) IDPs entering Earth’s atmosphere. Furthermore, because quasi-satellite trapping is known to be directly correlated with the host planet’s orbital eccentricity the accretion of quasi-satellite dust likely ebbs and flows on 10⁵ year time scales synchronized with Earth’s orbital evolution.     

An Observational Study of the Molecular Cloud Core Toward IRAS 23133+6050

This paper reports ¹³CO, C¹⁸O, HCO⁺ (J = 1−0) spectral observations toward IRAS 23133+6050 with the 13.7 m millimeter-wave telescope at Qinghai Station of PMO. Corresponding to the ¹³CO, C¹⁸O, HCO⁺ line emissions, the size of the observed molecular cloud core is 4.0 pc, 2.1 pc and 2.3 pc, the virial mass is 2.7 × 10³ M_⊙, 0.9 × 10³ M_⊙ and 2.3 × 10³ M_⊙, and the volume density of H₂ is 2.7 × 10³ cm⁻³, 5.1 × 10³ cm⁻³ and 4.6 × 10³ cm⁻³, respectively. Using the power-law function n(r) ∼r^−p, the spatial density distribution of the cloud core was analyzed, the obtained exponent p is respectively 1.75, 1.56 and 1.48 for the ¹³CO, C¹⁸O and HCO⁺ cores, and it is found that the density distribution becomes gradually flatter from the outer region to the inner region of the core. The HCO⁺ abundance is 4.6 × 10⁻¹⁰, one order of magnitude less than the value for dark clouds, and slightly less than that for giant molecular clouds. The ¹³CO/C¹⁸O relative abundance ratio is 12.2, comparable with the value 11.8 for dark clouds, and the value 9.0 ∼ 15.6 for giant molecular clouds. A ¹³CO bipolar outflow is found in this region. The IRAS far-infrared luminosity and the virial masses give the luminosity-mass ratios 18.1, 51.1 and 21.2 from the three lines.