Geochemistry of 4 Vesta based on HED meteorites: Prospective study for interpretation of gamma ray and neutron spectra for the Dawn mission

Abstract— Asteroid 4 Vesta, believed to be the parent body of the howardite, eucrite, and diogenite (HED) meteorites, will be investigated by the Dawn orbiting spacecraft. Dawn carries a gamma ray and neutron detector (GRaND) that will measure and map some major‐ and trace‐element abundances. Drawing on HED geochemistry, we propose a mixing model that uses element ratios appropriate for the interpretation of GRaND data. Because the spatial resolution of GRaND is relatively coarse, the analyzed chemical compositions on the surface of Vesta will likely reflect mixing of three endmember components: diogenite, cumulate eucrite, and basaltic eucrite. Reliability of the mixing model is statistically investigated based on published whole‐rock data for HED meteorites. We demonstrate that the mixing model can accurately estimate the abundances of all the GRaND‐analyzed major elements, as well as of minor elements (Na, Cr, and Mn) not analyzed by this instrument. We also show how a similar mixing model can determine the modal abundance of olivine, and we compare estimated and normative olivine data for olivine‐bearing diogenites. By linking the compositions of well‐analyzed HED meteorites with elemental mapping data from GRaND, this study may help constrain the geological context for HED meteorites and provide new insight into the magmatic evolution of Vesta.     

Using HED meteorites to interpret neutron and gamma‐ray data from asteroid 4 Vesta

Here, we construct a comprehensive howardite, eucrite, and diogenite (HED) bulk chemistry data set to compare with Dawn data. Using the bulk chemistry data set, we determine four gamma‐ray/neutron parameters in the HEDs (1) relative fast neutron counts (fast counts), (2) macroscopic thermal neutron absorption cross section (absorption), (3) a high‐energy gamma‐ray compositional parameter (C_p), and (4) Fe abundance. These correspond to the four measurements of Vesta made by Dawn's Gamma Ray and Neutron Detector (GRaND) that can be used to discern HED lithologic variability on the Vestan surface. We investigate covariance between fast counts and average atomic mass (<A>) in the meteorite data set, where a strong correlation (r² = 0.99) is observed, and we demonstrate that systematic offsets from the fast count/<A> trend are linked to changes in Fe and Ni concentrations. To compare the meteorite and GRaND data, we investigate and report covariance among fast counts, absorption, C_p, and Fe abundance in the HED meteorite data set. We identify several GRaND measurement spaces where the Yamato type B diogenites are distinct from all other HED lithologies, including polymict mixtures. The type B's are diogenites that are enriched in Fe + pigeonite + diopside ± plagioclase, relative to typical, orthopyroxenitic diogenites. We then compare these results to GRaND data and demonstrate that regions north of ~70°N latitude on Vesta (including the north pole) are consistent with type B diogenites. We propose two models to explain type B diogenite compositions in the north (1) deposition as Rheasilvia ejecta, or (2) type B plutons that were emplaced at shallow depths in the north polar region and sampled by local impacts. Lastly, using principal component (PC) analysis, we identify unique PC spaces for all HED lithologies, indicating that the corresponding GRaND measurables may be used to produce comprehensive lithologic maps for Vesta.     

Mixing relations of the howardite‐eucrite‐diogenite suite: A new statistical approach of independent component analysis for the Dawn mission

Dawn has recently revealed that the surface of Vesta is heterogeneously covered by polymictic regoliths represented by mixtures of howardite, eucrite, and diogenite (HED) meteorites. Mixing relations of the HED suite are examined here using a new computational statistical approach of independent component analysis (ICA). We performed eight‐component ICA (Si, Ti, Al, Cr, Fe, Mn, Mg, and Ca) for 209 HED bulk‐rock compositions. The ICA results indicate that the HED bulk‐rock compositions can be reduced into three independent components (IC) and these IC vectors can reasonably explain compositional variation, petrographic observations, and the mixing relations of the HED suite. The IC‐1 vector represents a eucrite variation that extends from cumulate eucrite toward main‐group (MG) and incompatible‐element enriched eucrites. The IC‐2 vector represents a compositional variation of howardites that extends from diogenites to MG‐eucrites, indicating the well‐known two‐component mixing trend of diogenite and eucrite. The IC‐3 vector represents a compositional variation defined by diogenites and olivine‐bearing diogenites, suggesting mixing of olivine and orthopyroxene. Among the three ICs, the diogenite‐eucrite mixing trend IC‐2 is most statistically robust and dominates the compositional variations of the HED suite. Our ICA study further indicates that the combination of only three elements (Mg, Si, and Fe) approximates the eight‐component ICA model, and that the limited number of resolvable γ‐ray spectra obtained by the Dawn mission possibly discriminates olivine lithologies from the olivine‐free regolith breccias on the surface of Vesta.     

Models for the X‐ray spectra and variability of luminous accreting black holes

The X‐ray spectra of luminous Seyfert 1 galaxies often appear to be reflection dominated. In a number of Narrow Line Seyfert 1 (NLS1) galaxies and galactic black holes in the very high state, the variability of the continuum and of the iron line are decoupled, the reflected component being often much less variable than the continuum. These properties have been interpreted as effects of gravitational light bending. In this framework, we present detailed Monte‐Carlo simulations of the reflection continuum in the Kerr metric. These calculations confirm that the spectra and variability behaviour of these sources can be reproduced by the light bending model. As an alternative to the light bending model, we show that similar observational properties are expected from radiation pressure dominated discs subject to violent clumping instabilities and, as a result, have a highly inhomogeneous two‐phase structure. In this model, most of the observed spectral and variability features originate from the complex geometrical structure of the inner regions of near‐Eddington accretion flows and are therefore a signature of accretion physics rather than general relativity. (© 2006 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Proper motion and X‐ray selected search for new members of the young TW Hya association

We have searched for new members of the TWHya association (TWA) among unidentified ROSAT X‐ray sources by identifying them in proper motion catalogues and selecting those that would be consistent with kinematical membership to the TWA. Spectroscopic follow‐up observations of 19 member candidates revealed the detection of moderate lithium absorption lines for the following three stars: GSC 7206 845, TYC 7216‐55, and TYC 7247‐12. The isochronal ages of the latter TYC stars are estimated to be ∼20 Myr while the other one has ∼100 Myr age based on a kinematic distance estimate that assumes TWA membership. However, the moderately Li‐rich stars are not likely to be new pre‐main sequence members of TWA partly because of the discrepant radial velocities. Infrared follow‐up imaging in the H‐band for the 3 stars shows companion candidates near two of them.While one system (TYC 7216‐55) is probably a near‐equal‐magnitude stellar binary, our follow‐up H‐band spectrum of the faint companion candidate near GSC 7206 845 shows that it is instead a background K‐type star rather than a companion. (© 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

In situ micro‐Raman and X‐ray diffraction study of diamonds and petrology of the new ureilite UAE 001 from the United Arab Emirates

Abstract— A new olivine‐pigeonite ureilite containing abundant diamonds and graphite was found in the United Arab Emirates. This is the first report of a meteorite in this country. The sample is heavily altered, of medium shock level, and has a total weight of 155 g. Bulk rock, olivine (Fo_79.8–81.8) and pyroxene (En_73.9–75.2, Fs_15.5–16.9, Wo_8.8–9.5) compositions are typical of ureilites. Olivine rims are reduced with Fo increasing up to Fo_96.1–96.8. Metal in these rims is completely altered to Fehydroxide during terrestrial weathering. We studied diamond and graphite using micro‐Raman and in situ synchrotron X‐ray diffraction. The main diamond Raman band (LO = TO mode at ?1332 cm^?1) is broadened when compared to well‐ordered diamond single crystals. Full widths at half maximum (FWHM) values scatter around 7 cm^?1. These values resemble FWHM values obtained from chemical vapor deposition (CVD) diamond. In situ XRD measurements show that diamonds have large grain sizes, up to >5 μm. Some of the graphite measured is compressed graphite. We explore the possibilities of CVD versus impact shock origin of diamonds and conclude that a shock origin is much more plausible. The broadening of the Raman bands might be explained by prolonged shock pressure resulting in a transitional Raman signal between experimentally shock‐produced and natural diamonds.     

Comparison of FT‐IR spectra of bulk and acid insoluble organic matter in chondritic meteorites: An implication for missing carbon during demineralization

Past studies of the various separable carbonaceous fractions have been unable to account for all of C in primitive chondrites. In particular, up to 20–50% of the C is lost during acid leaching of bulk samples even after the C in carbonates and soluble organic matter is accounted for. To try to better characterize the nature of this “missing C,” we have compared the bulk infrared (IR) absorption spectra of a number of primitive chondrites with those of their previously reported insoluble organic matter (IOM). The aliphatic C–H stretching bands, in particular, allow us to compare the molecular structures of bulk C with that of IOM. The spectral differences between bulk C and IOM reflect “missing C” phases that were lost during acid leaching, although we cannot completely exclude the possibility that the OM was modified after demineralization. Comparing IR spectra of bulk meteorite powder and IOM suggests that the missing C varies in its molecular structure, and that mildly thermally metamorphosed type 3 chondrites tend to be richer in an aliphatic fraction with lower CH₂/CH₃ ratios, relative to IOM, compared to aqueously altered carbonaceous chondrites (CI/CM/CR). The missing C is most likely released from acid‐labile functional groups, such as esters, acetals, and amides, during demineralization, although it cannot be ruled out that some fraction of the missing C is in small grains that are difficult to recover from suspension, or in water‐soluble compounds trapped in phyllosilicates.     

The Miller Range 090340 and 090206 meteorites: Identification of new brachinite‐like achondrites with implications for the diversity and petrogenesis of the brachinite clan

Miller Range (MIL) 090340 and MIL 090206 are olivine‐rich achondrites originally classified as ureilites. We investigate their petrography, mineral compositions, olivine Cr valences, equilibration temperatures, and (for MIL 090340) oxygen isotope compositions, and compare them with ureilites and other olivine‐rich achondrites. We conclude that they are brachinite‐like achondrites that provide new insights into the petrogenesis of brachinite clan meteorites. MIL 090340,6 has a granoblastic texture and consists of ~97 modal % by area olivine (Fo = molar Mg/[Mg+Fe] = 71.3 ± 0.6). It also contains minor to trace augite, chromite, chlorapatite, orthopyroxene, metal, troilite, and terrestrial Fe‐oxides. Approximately 80% by area of MIL 090206,5 has a granoblastic texture of olivine (Fo 72.3 ± 0.1) plus minor augite and chromite, similar to MIL 090340 but also containing minor plagioclase. The rest of the section consists of a single crystal of orthopyroxene (~11 × 3 mm), poikilitically enclosing rounded grains of olivine (Fo = 76.1 ± 0.6), augite, chromite, metal, and sulfide. Equilibration temperatures for MIL 090340 and MIL 090206, calculated from olivine‐spinel, olivine‐augite, and two‐pyroxene thermometry range from ~800 to 930 °C. In both samples, symplectic intergrowths of Ca‐poor orthopyroxene + opaque phases (Fe‐oxides, sulfide, metal) occur as rims on and veins/patches within olivine. Before terrestrial weathering, the opaques were probably mostly sulfide, with minor metal. All petrologic properties of MIL 090340 and MIL 090206 are consistent with those of brachinite clan meteorites, and largely distinct from those of ureilites. Oxygen isotope compositions of olivine in MIL 090340 (δ¹⁸O = 5.08 ± 0.30‰, δ¹⁷O = 2.44 ± 0.21‰, and Δ¹⁷O = ?0.20 ± 0.12‰) are also within the range of brachinite clan meteorites, and well distinguished from ureilites. Olivine Cr valences in MIL 090340 and the granoblastic area of MIL 090206 are 2.57 ± 0.06 and 2.59 ± 0.07, respectively, similar to those of three brachinites also analyzed here (Brachina, Hughes 026, Nova 003). They are higher than those of olivine in ureilites, even those containing chromite. The valence systematics of MIL 090340, MIL 090206, and the three analyzed brachinites (lower Fo = more oxidized Cr) are consistent with previous evidence that brachinite‐like parent bodies were inherently more oxidized than the ureilite parent body. The symplectic orthopyroxene + sulfide/metal assemblages in MIL 090340, MIL 090206, and many brachinite clan meteorites have superficial similarities to characteristic “reduction rims” in ureilites. However, they differ significantly in detail. They likely formed by reaction of olivine with S‐rich fluids, with only minor reduction. MIL 090340 and the granoblastic area of MIL 090206 are similar in modal mineralogy and texture to most brachinites, but have higher Fo values typical of brachinite‐like achondrites. The poikilitic pyroxene area of MIL 090206 is more typical of brachinite‐like achondrites. The majority of their properties suggest that MIL 090340 and MIL 090206 are residues of low‐degree partial melting. The poikilitic area of MIL 090206 could be a result of limited melt migration, with trapping and recrystallization of a small volume of melt in the residual matrix. These two samples are so similar in mineral compositions, Cr valence, and cosmic ray exposure ages that they could be derived from the same lithologic unit on a common parent body.     

A new model for the origin of Type‐B and Fluffy Type‐A CAIs: Analogies to remelted compound chondrules

Abstract– In the scenario developed here, most types of calcium‐aluminum‐rich inclusions (CAIs) formed near the Sun where they developed Wark‐Lovering rims before being transported by aerodynamic forces throughout the nebula. The amount of ambient dust in the nebula varied with heliocentric distance, peaking in the CV–CK formation location. Literature data show that accretionary rims (which occur outside the Wark‐Lovering rims) around CAIs contain substantial ¹⁶O‐rich forsterite, suggesting that, at this time, the ambient dust in the nebula consisted largely of ¹⁶O‐rich forsterite. Individual sub‐millimeter‐size Compact Type‐A CAIs (each surrounded by a Wark‐Lovering rim) collided in the CV–CK region and stuck together (in a manner similar to that of sibling compound chondrules); the CTAs were mixed with small amounts of ¹⁶O‐rich mafic dust and formed centimeter‐size compound objects (large Fluffy Type‐A CAIs) after experiencing minor melting. In contrast to other types of CAIs, centimeter‐size Type‐B CAIs formed directly in the CV–CK region after gehlenite‐rich Compact Type‐A CAIs collided and stuck together, incorporated significant amounts of ¹⁶O‐rich forsteritic dust (on the order of 10–15%) and probably some anorthite, and experienced extensive melting and partial evaporation. (Enveloping compound chondrules formed in an analogous manner.) In those cases where appreciably higher amounts of ¹⁶O‐rich forsterite (on the order of 25%) (and perhaps minor anorthite and pyroxene) were incorporated into compound Type‐A objects prior to melting, centimeter‐size forsterite‐bearing Type‐B CAIs (B3 inclusions) were produced. Type‐B1 inclusions formed from B2 inclusions that collided with and stuck to melilite‐rich Compact Type‐A CAIs and experienced high‐temperature processing.     

A Mössbauer spectroscopy and X‐ray diffraction study of ordinary chondrites: Quantification of modal mineralogy and implications for redox conditions during metamorphism

Abstract— We present a method that combines Mössbauer spectroscopy and X‐ray diffraction to quantify the modal mineralogy of unequilibrated ordinary chondrites (UOCs). Despite being a fundamental tool in the interpretation of geological systems, there are no modal mineralogical data available for these meteorites. This is due to their fine‐grained nature, highly heterogeneous silicate mineralogy, and the presence of poorly characterized phases. Consequently, it has not been possible to obtain accurate modal mineralogy by conventional techniques such as point counting. Here we use Mössbauer spectroscopy as a preliminary identification technique and X‐ray diffraction provides the quantification for a suite of recent UOC falls. We find the most primitive UOCs to contain a significant amount of phyllosilicate material that was converted during metamorphism to form ferromagnesian silicates. A complete suite of Antarctic samples is analyzed by each method to observe mineralogical trends and these are compared with trends shown by recent falls. The fact that mineralogical relationships shown by finds and falls are in agreement allows us to be confident that we are observing the products of pre‐terrestrial alteration. Mössbauer spectroscopy reveals evidence of steadily increasing reduction with metamorphism in the UOCs. Because this technique allows comparisons to be made between UOCs and EOCs, our reduction sequence can be combined with other evidence showing progressive oxidation in the EOCs. This yields an integrated model of changing redox conditions on equilibrating ordinary chondrite parent bodies.     

Strontium and neodymium isotopic study of Libyan Desert Glass: Inherited Pan‐African age signatures and new evidence for target material

Abstract— Libyan Desert Glass (LDG) is an impact‐related, natural glass of still unknown target material. We have determined Rb‐Sr and Sm‐Nd isotopic ratios from seven LDG samples and five associated sandstones from the LDG strewn field in the Great Sand Sea, western Egypt. Planar deformation features were recently detected in quartz from these sandstones. ⁸⁷Sr/⁸⁶Sr ratios and ?‐Nd values for LDG range between 0.71219 and 0.71344, and between –16.6 and –17.8, respectively, and hence are distinct from the less radiogenic ⁸⁷Sr/⁸⁶Sr ratios of 0.70910–0.71053 and ?‐Nd values from –6.9 to –9.6 for the local sandstones from the LDG strewn field. Previously published isotopic ratios from the Libyan BP and Oasis crater sandstones are generally incompatible with our LDG values. LDG formation undoubtedly occurred at 29 Ma, but neither the Rb‐Sr nor the Sm‐Nd isotopic system were rehomogenised during the impact event, as we can deduce from Pan‐African ages of ?540 Ma determined from the regression lines from a total of 14 LDG samples from this work and the literature. Together with similar Sr and Nd isotopic values for LDG and granitoid rocks from northeast Africa west of the Nile, these findings point to a sandy matrix target material for the LDG derived from a Precambrian crystalline basement, ruling out the Cretaceous sandstones of the former “Nubian Group” as possible precursors for LDG.