Mineralogy and petrology of the angrite Northwest Africa 1296

Abstract— We report on a new angrite, Northwest Africa (NWA) 1296, a fine‐grained rock with a magmatic texture of rapid cooling. Dendritic olivine (?Fo₅₀) crystallized first in association with anorthite microcrysts (An_98–100) forming composite chains separated from one another by intergrown Al‐Fe diopside‐hedenbergite pyroxenes. In addition, some olivines with lower Mg# and increased CaO (up to 12%) are found between the chains as equant microphenocrysts. Pyroxenes and olivines are both normally zoned from Mg# = 0.52 to less than 0.01 in the rims. Ca‐rich olivines are surrounded by, intergrown with, or replaced by subcalcic kirschsteinite. They appear after plagioclase crystallization stopped, at the end of the crystallization sequence. Minor phases are pyrrhotite, F‐apatite, and titanomagnetite. Pyroxene is the last silicate phase to grow, interstitial to idiomorphic olivine‐kirschsteinite. Numerous small vesicles and some channels are filled with microcristalline carbonate. The mode (vol%) is about 28% olivine, 3% kirschsteinite, 32% anorthite, 34% pyroxene, and 3% of the minor phases—close to that reported previously for D'Orbigny and Sahara (SAH) 99555. The bulk chemical composition of NWA 1296 is similar to D'Orbigny and SAH 99555; NWA 1296 differs by its texture and mineralogy, which are interpreted as resulting from rapid crystallization—an evidence of impact melting. Angrites cannot be produced by partial melting of a CV source because segregation of a “planetary” core is necessary to explain the low FeO/MgO ratio of magnesian olivines. Neither the odd Ca/Al ratio nor the very low SiO₂ content can be explained by conventional partial melting scenarios. We suggest that carbonate is the key to angrite genesis. This is supported by the striking similarities with terrestrial melilitites (low SiO₂, superchondritic Ca/Al ratio, presence of carbonate). The lack of alkalies could be the result of either loss after impact melting or absence of alkalies in the source.     

Nickel abundance in stony cosmic spherules: Constraining precursor material and formation mechanisms

Abstract– We report bulk and olivine compositions in 66 stony cosmic spherules (Na₂O < 0.76 wt%), 200–800 μm in size, from the Transantarctic Mountains, Antarctica. In porphyritic cosmic spherules, relict olivines that survived atmospheric entry heating are always Ni‐poor and similar in composition to the olivines in carbonaceous or unequilibrated ordinary chondrites (18 spherules), and equilibrated ordinary chondrites (one spherule). This is consistent with selective survival of high temperature, Mg‐rich olivines during atmospheric entry. Olivines that crystallized from the melts produced during atmospheric entry have NiO contents that increase with increasing NiO in the bulk spherule, and that range from values similar to those observed in chondritic olivines (NiO generally <0.5 wt%) to values characteristic of olivines in meteoritic ablation spheres (NiO > 2 wt%). Thus, NiO content in olivine cannot be used alone to distinguish meteoritic ablation spheres from cosmic spherules, and the volatile element contents have to be considered. We propose that the variation in NiO contents in cosmic spherules and their olivines is the result of variable content of Fe, Ni metal in the precursor. NiO contents in olivines and in cosmic spherules can thus be used to discuss their parent body. Ni‐poor spherules can be derived from C‐rich and/or metal‐poor precursors, either related to CM, CI, CR chondrites or to chondritic fragments dominated by silicates, regardless of the parent body. Ni‐rich spherules (NiO > 0.7 wt%) that represent 55% of the 47 barred‐olivine spherules we studied, were derived from the melting of C‐poor, metal‐rich precursors, compatible with ordinary chondrite or CO, CV, CK carbonaceous chondrite parentages.     

AN UNEQUILIBRATED INCLUSION IN THE ROMERO (H3–4) CHONDRITE

Within the chondritic matrix of Romero (H3–4) is a metal-poor inclusion consisting largely of olivines showing quench textures, minor low-Ca pyroxene and rare metal and sulphide. The olivines within this inclusion have the dominant composition Fa⁸ with a range Fa^{7, 5–17}. The matrix (Romero host) olivines are, in the main, equilibrated with an average composition of Fa¹⁸, but are lower in CaO and Cr²O³ than the inclusion olivines. The high chromium content of the inclusion olivines suggests that they formed under conditions different from those represented by the other olivines in Romero.     

Trace elements in olivine and the petrogenesis of the intermediate,olivine‐phyric shergottite NWA 10170

Olivine‐phyric shergottites represent primitive basaltic to picritic rocks, spanning a large range of Mg# and olivine abundances. As primitive olivine‐bearing magmas are commonly representative of their mantle source on Earth, understanding the petrology and evolution of olivine‐phyric shergottites is critical in our understanding of Martian mantle compositions. We present data for the olivine‐phyric shergottite Northwest Africa (NWA) 10170 to constrain the petrology with specific implications for magma plumbing‐system dynamics. The calculated oxygen fugacity and bulk‐rock REE concentrations (based on modal abundance) are consistent with a geochemically intermediate classification for NWA 10170, and overall similarity with NWA 6234. In addition, we present trace element data using laser ablation ICP‐MS for coarse‐grained olivine cores, and compare these data with terrestrial and Martian data sets. The olivines in NWA 10170 contain cores with compositions of Fo₇₇ that evolve to rims with composition of Fo₅₈, and are characterized by cores with low Ni contents (400–600 ppm). Nickel is compatible in olivine and such low Ni content for olivine cores in NWA 10170 suggests either early‐stage fractionation and loss of olivine from the magma in a staging chamber at depth, or that Martian magmas have lower Ni than terrestrial magmas. We suggest that both are true in this case. Therefore, the magma does not represent a primary mantle melt, but rather has undergone 10–15% fractionation in a staging chamber prior to extrusion/intrusion at the surface of Mars. This further implies that careful evaluation of not only the Mg# but also the trace element concentrations of olivine needs to be conducted to evaluate pristine mantle melts versus those that have fractionated olivine (±pyroxene and oxide minerals) in staging chambers.     

Ararki (L5) chondrite: The first meteorite find in Thar Desert of India

Abstract— We report here a chance find of a meteorite in the sand dunes of Ararki village of Hanumangarh district in the Rajasthan desert of northwest India. Chemical and petrological evidence in conjunction with isotopic composition of oxygen indicate that it is an L5 chondrite. The fayalite content of olivines is 26.3 mol%. The meteorite has some serpentinized olivines and 0.3% carbon having a terrestrial isotopic composition, indicating that it is moderately weathered. The absence of ²²Na indicate that the meteorite fell to Earth more than a decade ago. The cosmic‐ray exposure age based on cosmogenic ²¹Ne is 7.2 Ma. Low density of cosmic‐ray heavy nuclei tracks, low ²⁶A1 activity, the shielding parameter [(²²Ne/²¹Ne)_C = 1.094] and absence of neutron capture effects indicate cosmic‐ray shielding in a meteoroid having radius of about 16 cm, implying a meteoroid mass of about 60 kg and ablation of about 93%. The gas retention ages, based on U/Th‐⁴He and K‐⁴⁰Ar are 1.1 and 0.58 Ga, respectively, suggesting a heating and degassing event late in the history of this meteorite.     

Terrestrial ages of ordinary chondrites from the Lewis Cliff stranding area,East Antarctica

Abstract— We determined terrestrial ages of ordinary chondrites from the Lewis Cliff stranding area, East Antarctica, on the basis of the concentrations of cosmogenic ¹⁰Be (t_½; = 1.51 Ma), ²⁶Al (t_½; = 0.705 Ma), and ³⁶Cl (t_½; = 0.301 Ma). After an initial ²⁶Al γ-ray survey of 91 meteorites suggested that many have terrestrial ages >0.1 Ma, we selected 62 meteorites for ¹⁰Be and ²⁶Al measurements by accelerator mass spectrometry (AMS) and measured ³⁶Cl in twelve of those. Low terrestrial ages (<0.1 Ma) were found for ～60% of the meteorites, whereas all others have ages between 0.1 and 0.5 Ma, except for one exceptional age of >2 Ma (Welten et al., 1997). Our major conclusions are: (1) The Lewis Cliff H-chondrites show similar ages to those from the Allan Hills icefields, but the L-chondrites are about a factor of 2 younger than those from Allan Hills, which indicates that Lewis Cliff is a younger stranding area. (2) The terrestrial age distributions at different parts of the Lewis Cliff stranding area generally agree with simple meteorite concentration models, although differences in weathering rate may also play a role. (3) We confirm that meteorites with natural thermoluminescence (TL) levels >80 krad are associated with low terrestrial ages (Benoit et al., 1992) but conclude that natural TL levels <80 krad can not be used to calculate the terrestrial age of a meteorite. Natural TL levels do seem useful to estimate relative terrestrial ages of large groups of meteorites and to determine differences in the surface exposure age of paired meteorite fragments. (4) Of the 62 meteorites measured with AMS, 31 were assigned to 11 different pairing groups, mainly on the basis of their cosmogenic nuclide record. The meteorites are estimated to represent between 42 and 52 distinct falls.     

Experimental study and TEM characterization of dusty olivines in chondrites: Evidence for formation by in situ reduction

Abstract— An analytical transmission electron microscopy (ATEM) study was undertaken in order to better understand the formation conditions of dusty olivines (i.e., olivines containing abundant tiny inclusions of Fe‐Ni metal) in primitive meteorites. Dusty olivines from type I chondrules in the Bishunpur chondrite (LL3.1) and from synthetic samples obtained by reduction of San Carlos olivines were examined. In both natural and experimental samples, micron size metal blebs observed in the dusty region often show preferential alignments along crystallographic directions of the olivine grains, have low Ni contents (typically <2 wt%), and are frequently surrounded by a silica‐rich glass layer. These features suggest that dusty olivines are formed by a sub‐solidus reduction of initially fayalitic olivines according to the following reaction: Some volatilization of SiO_gas may account for the apparent excess of metal relative to silica‐rich glass observed in both experimental and natural samples. Comparison with experimentally produced dusty olivines suggests that time scales of the order of minutes usually inferred for chondrule formation are also adequate for the formation of dusty olivines. These observations are in agreement with the hypothesis that at least part of the metal phase in chondrites originated from reduction during chondrule formation.     

Chemical and isotopic characteristics of the Didwana‐Rajod (H5) chondrite

Abstract— The mineralogical and chemical characteristics of the Didwana‐Rajod chondrite are described. The mean mineral composition is found to be olivine (Fo_83.2) and pyroxene (En_83.5Wo_0.7Fs_15.8), and feldspar is mainly oligoclase. Oxygen isotopic analysis shows δ¹⁸O = +3.8%0 and δ¹⁷O = +2.59%0. The nitrogen content of Didwana‐Rajod is ～2 ppm with δ¹⁵N ? 3.4%0. Based on microscopic, chemical, isotopic and electron probe microanalysis, the meteorite is classified as an H5 chondrite. Cosmogenic tracks, radionuclides and the isotopic composition of rare gases were also measured in this meteorite. The track density in olivines varies in a narrow range with an average value of (6.5 ± 0.5) × 10⁵/cm² for four spot samples taken at the four corners of the stone. The cosmic‐ray exposure age based on neon and argon is 9.8 Ma. ²²Na/²⁶Al ? 0.94 is lower than the solar‐cycle average value of ～1.5 and is consistent with irradiation of the meteoroid to lower galactic cosmic‐ray fluxes as expected at the solar maximum. The track density, rare gas isotopic ratios, ⁶⁰Co activity and other radionuclide data are consistent with a preatmospheric radius of ～15 cm, corresponding to a mass of ～50 kg. The cosmogenic properties are consistent with a simple exposure history in interplanetary space.     

Roosevelt County 075: A petrologic,chemical and isotopic study of the most unequilibrated known H chondrite

Abstract— Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite, δ¹³C). Petrologic subtype 3.2± 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most unequilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.     

Oxygen isotopes in chondrule olivine and isolated olivine grains from the CO3 chondrite Allan Hills A77307

Abstract— We have measured O‐isotopic ratios in a variety of olivine grains in the CO3 chondrite Allan Hills (ALH) A77307 using secondary ion mass spectrometry in order to study the chondrule formation process and the origin of isolated olivine grains in unequilibrated chondrites. Oxygen‐isotopic ratios of olivines in this chondrite are variable from δ¹⁷O = ?15.5 to +4.5% and δ¹⁸O = ?11.5 to +3.9%, with Δ¹⁷O varying from ?10.4 to +3.5%. Forsteritic olivines, Fa_<1, are enriched in ¹⁶O relative to the bulk chondrite, whereas more FeO‐rich olivines are more depleted in ¹⁶O. Most ratios lie close to the carbonaceous chondrite anhydrous minerals (CCAM) line with negative values of Δ¹⁷O, although one grain of composition Fa₄ has a mean Δ¹⁷O of +1.6%. Marked O‐isotopic heterogeneity within one FeO‐rich chondrule is the result of incorporation of relic, ¹⁶O‐rich, Mg‐rich grains into a more ¹⁶O‐depleted host. Isolated olivine grains, including isolated forsterites, have similar O‐isotopic ratios to olivine in chondrules of corresponding chemical composition. This is consistent with derivation of isolated olivine from chondrules, as well as the possibility that isolated grains are chondrule precursors. The high ¹⁶O in forsteritic olivine is similar to that observed in forsterite in CV and CI chondrites and the ordinary chondrite Julesburg and suggests nebula‐wide processes for the origin of forsterite that appears to be a primitive nebular component.     

Mid‐infrared study of stones from the Sutter's Mill meteorite

The Sutter's Mill meteorite fell in northern California on April 22, 2012. Several fragments of the meteorite were recovered, some of them shortly after the fall, others several days later after a heavy rainstorm. In this work, we analyzed several samples of four fragments―SM2, SM12, SM20, and SM30―from the Sutter's Mill meteorite with two infrared (IR) microscopes operating in the 4000–650 cm^?1 (2.5–15.4 μm) range. Spectra show absorption features associated with minerals such as olivines, phyllosilicates, carbonates, and possibly pyroxenes, as well as organics. Spectra of specific minerals vary from one particle to another within a given stone, and even within a single particle, indicating a nonuniform mineral composition. Infrared features associated with aliphatic CH₂ and CH₃ groups associated with organics are also seen in several spectra. However, the presence of organics in the samples studied is not clear because these features overlap with carbonate overtone bands. Finally, other samples collected within days after the rainstorm show evidence for bacterial terrestrial contamination, which indicates how quickly meteorites can be contaminated on such small scales.     

Correlations and zoning patterns of phosphorus and chromium in olivine from H chondrites and the LL chondrite Semarkona

Phosphorus zoning is observed in olivines in high‐FeO (type IIA) chondrules in H chondrites over the entire range of petrologic grades: H3.1–H6. Features in P concentrations such as oscillatory and sector zoning, and high P cores are present in olivines that are otherwise unzoned in the divalent cations. Aluminum concentrations are low and not significantly associated with P zoning in chondrule olivines. In highly unequilibrated H chondrites, phosphorus zoning is generally positively correlated with Cr. Atomic Cr:P in olivine is roughly 1:1 (3:1 for one zone in one olivine in RC 075), consistent with Cr³⁺ charge‐balancing P⁵⁺ substituting for Si⁴⁺. Normal igneous zonation involving the dominant chrome species Cr²⁺ was observed only in the LL3.0 chondrite Semarkona. In more equilibrated chondrites (H3.5–H3.8), Cr spatially correlated with P is occasionally observed but it is diffuse relative to the P zones. In H4–H6 chondrites, P‐correlated Cr is absent. One signature of higher metamorphic grades (≥H3.8) is the presence of near matrix olivines that are devoid of P oscillatory zoning. The restriction to relatively high metamorphic grade and to grains near the chondrule–matrix interface suggests that this is a response to metasomatic processes. We also observed P‐enriched halos near the chondrule–matrix interface in H3.3–H3.8 chondrites, likely reflecting the loss of P and Ca from mesostasis and precipitation of Ca phosphate near the chondrule surface. These halos are absent in equilibrated chondrites due to coarsening of the phosphate and in unequilibrated chondrites due to low degrees of metasomatism. Olivines in type IA chondrules show none of the P‐zoning ubiquitous in type IIA chondrules or terrestrial igneous olivines, likely reflecting sequestration of P in reduced form within metallic alloys and sulfides during melting of type IA chondrules.     

Deconvolution of lunar olivine reflectance spectra: Implications for remote compositional assessment

Lunar olivines typically contain inclusions of Cr-spinel (chromite) that influence their measured optical properties. These altered optical properties complicate modeled predictions of olivine composition from reflectance spectra. Approaches developed for inclusion-free terrestrial olivine spectra must be modified to be applied to chromite-bearing lunar olivine spectra. We present a revised approach for predicting the compositions of chromite-bearing lunar olivines using the Modified Gaussian Model (MGM). The results of this revised approach for chromite-bearing lunar olivines are consistent with previous results for terrestrial olivine reflectance spectra, and successfully predict the olivine’s composition. These results are an important step in compositional assessment of remotely-sensed olivine spectra, and are essential to ongoing investigations of that topic. Our results are based on a limited set of available lunar olivine separates, and would be strengthened by the inclusion of additional compositions.     

Origin of fayalitic olivine rims and lath-shaped matrix olivine in the CV3 chondrite Allende and its dark inclusions

Abstract— We have studied an Allende dark inclusion by optical microscopy, scanning electron microscopy, electron microprobe analysis and transmission electron microscopy. The inclusion consists of chondrules, isolated olivines and matrix, which, as in the Allende host, is mainly composed of 5–20 μm long lath-shaped fayalitic grains with a narrow compositional range (Fa_{42 ± 2}) and nepheline. Olivine phenocrysts in chondrules and isolated olivine grains show various degrees of replacement by 5–10 μm wide fayalitic rims (Fa_{39 ± 2}) and 100–1000 μm wide translucent zones, which consist of 5–20 μm long lath-shaped fayalitic grains (Fa_{41 ± 1}) intergrown with nepheline. These fayalitic olivines, like those in the matrix of the dark inclusion, contain 10–20 nm sized inclusions of chromite, hercynite, and Fe-Ni sulfides. The fayalitic rims around remnant olivines are texturally and compositionally identical to those in Allende host, suggesting that they have similar origins. Chondrules are surrounded by opaque rims consisting of tiny lath-shaped fayalitic olivines (<1–3 μm long) intergrown with nepheline. As in the Allende host, fayalitic olivine veins may crosscut altered chondrules, fine-grained chondrule rims and extend into the matrix, indicating that alteration occurred after accretion. We infer that fayalitic olivine rims and lath-shaped fayalites in Allende and its dark inclusions formed from phyllosilicate intermediate phases. This explanation accounts for (1) the similarity of the replacement textures observed in the dark inclusion and Allende host to aqueous alteration textures in CM chondrites; (2) the anomalously high abundances of Al and Cr and the presence of tiny inclusions of spinels and sulfides in fayalitic olivines in Allende and Allende dark inclusions; (3) abundant voids and defects in lath-shaped fayalites in the Allende dark inclusion, which may be analogous to those in partly dehydrated phyllosilicates in metamorphosed CM/CI chondrites. We conclude that the matrix and chondrule rims in Allende were largely converted to phyllosilicates and then completely dehydrated. The Allende dark inclusions experienced diverse degrees of aqueous/hydrothermal alteration prior to complete dehydration. The absence of low-Ca pyroxene in the dark inclusion and its significant replacement by fayalitic olivine in Allende is consistent with the lower resistance of low-Ca pyroxene to aqueous alteration relative to forsteritic olivine. Hydro-thermal processing of Allende probably also accounts for the low abundance of planetary noble gases and interstellar grains, and the formation of nepheline, sodalite, salite-hedenbergite pyroxenes, wollastonite, kirschsteinite and andradite in chondrules and Ca,Al-rich inclusions.     

MgAl2O4 spinels from Allende and NWA 763 carbonaceous chondrites: Structural refinement,cooling history,and trace element contents

MgAl₂O₄ spinels from Allende and NWA 763 carbonaceous chondrites were studied by X‐ray single crystal diffraction, SEM, electron microprobe, LA‐ICP‐MS, and Raman spectroscopy. Those from Allende are almost pure, but, in one case, we found a strong FeO_tot zonation. Spinels from NWA 763 show Mg‐Fe²⁺ substitutions. Almost pure MgAl₂O₄ spinels from both meteorites underwent slow cooling and reached their intracrystalline closure temperature (T_c) in the range 460–520 °C. The NWA 763 spinel with higher FeO content shows a T_c of about 720 °C. X‐ray single crystal diffraction and Raman spectroscopy suggest a slow cooling and an ordered structure with trivalent cations in M site and divalent in T site. Among the trace elements, Ti and Co are enriched with respect to the terrestrial analogs, while Mn, Ni, and Sn show intermediate values between different terrestrial occurrences. Vanadium cannot be used as a tracer of extraterrestrial origin as for Cr‐spinels, because its content is similar in extraterrestrial and terrestrial spinels. In the zoned crystal from Allende, Co show a strong zonation similar to that of FeO.     

Lithium isotopes and light lithophile element abundances in shergottites: Evidence for both magmatic degassing and subsolidus diffusion

Degassed magmatic water was potentially the major source of surficial water on Mars. We measured Li, B, and Be abundances and Li isotope profiles in pyroxenes, olivines, and maskelynite from four compositionally different shergottites—Shergotty, QUE 94201, LAR 06319, and Tissint—using secondary ion mass spectrometry (SIMS). All three light lithophile elements (LLE) are incompatible: Li and B are soluble in H₂O‐rich fluids, whereas Be is insoluble. In the analyzed shergottites, Li concentration decreases and Be concentration increases from cores to rims in pyroxenes. However, B concentrations do not vary consistently with Li and Be abundances, except in QUE 94201 pyroxenes. Additionally, abundances of these three elements in olivines show a normal igneous‐fractionation trend consistent with the crystallization of olivine before magma ascent and degassing. We expect that kinetic effects would lead to fractionation of ⁶Li in the vapor phase compared to ⁷Li during degassing. The Li isotope profiles, with increasing δ⁷Li from cores to rims, as well as Li and B profiles indicate possible degassing of hydrous fluids only for the depleted shergottite QUE 94201, as also supported by degassing models. Conversely, Shergotty, LAR 06319, and Tissint appear to have been affected by postcrystallization diffusion, based on their LLE and Li isotope profiles, accompanied by diffusion models. This process may represent an overlay on a degassing pattern. The LLE profiles and isotope profiles in QUE 94201 support the hypothesis that degassing of some basaltic shergottite magmas provided water to the Martian surface, although evidence may be obscured by subsolidus diffusion processes.     

THE COLONY METEORITE AND VARIATIONS IN CO3 CHONDRITE PROPERTIES

The Colony meteorite is an accretionary breccia containing several millimeter-to centimeter-size chondritic clasts embedded in a chondritic host. Colony is one of the least equilibrated CO3 chondrites; it has an unrecrystallized texture and contains compositionally heterogeneous olivine and low-Ca pyroxene, kamacite with low Ni and Co and high Cr, amoeboid inclusions with low FeO and MnO, a fine-grained silicate matrix with very high FeO, and numerous small chondrules with clear pink glass. However, Colony differs from normal CO chondrites in several respects: Although Al, Sc, V, Cr, Ir, Fe, Au and Ga abundances are consistent with a CO chondrite classification, certain lithophiles (Mg and Mn), siderophiles (Ni and Co) and chalcophiles (Se and Zn) are depleted by factors of 10–40%. The shape of Colony's thermoluminescence (TL) glow curve is similar to that of Allan Hills A77307 (another unequilibrated chondrite with CO3 petrological characteristics) and different from those of normal CO chondrites. [ALHA77307 also resembles Colony in having low Mg, Mn, Ni and Co, compared to normal CO chondrites, but it possesses CO-CV levels of Se and Zn and nearly CV levels of Cd.] Colony is badly weathered; it contains 22.7 wt.% Fe₂O₃ and 5.7 wt.% H₂O. Recalculating the analysis on an H₂O-free basis with all Fe₂O₃, NiO and CoO converted to metal, yields an inferred original metallic Fe, Ni abundance of ～ 19 wt.%. This is similar to that of Kainsaz (an unweathered CO3 fall), but much higher than that of all other CO3 chondrites (< 6.3 wt.%). Although it is possible that Colony and either ALHA77307 or Kainsaz constitute distinct CO3 chemical subgroups, the weathered nature of Colony and ALHA77307 preclude the drawing of firm conclusions. Nevertheless, it is clear that CO3 chondrites vary more in compositional and petrological properties than was previously recognized.     

Oxygen isotopes in magnetite and fayalite in CV chondrites Kaba and Mokoia

Abstract— We report in situ measurements of O‐isotopic compositions of magnetite and primary and secondary olivine in the highly unequilibrated oxidized CV chondrites Kaba and Mokoia. In both meteorites, the magnetite and the secondary olivine (fayalite, Fa_90–100) have O‐isotopic compositions near the terrestrial fractionation (TF) line; the mean Δ¹⁷O (= δ¹⁷O‐0.52 × δ¹⁸O) value is about ?1%‰. In contrast, the compositions of nearby primary (chondrule), low‐FeO olivines (Fa_1–2) are well below the TF line; Δ¹⁷O values range from ?3 to ?9%‰. Krot et al. (1998) summarized evidence indicating that the secondary phases in these chondrites formed by aqueous alteration in an asteroidal setting. The compositions of magnetite and fayalite in Kaba and Mokoia imply that the O‐isotopic composition of the oxidant was near or somewhat above the TF line. In Mokoia the fayalite and magnetite differ in δ¹⁸O by ～20%‰, whereas these same materials in Kaba have virtually identical compositions. The difference between Mokoia magnetite and fayalite may indicate formation in isotopic equilibrium in a water‐rich environment at low temperatures, ～300 K. In contrast, the similar compositions of these phases in Kaba may indicate formation of the fayalite by replacement of preexisting magnetite in dry environment, with the O coming entirely from the precursor magnetite and silica. The Δ¹⁷O of the oxidant incorporated into the CV parent body (as phyllosilicates or H₂O) appears to have been much (7–8%‰) lower than that in that incorporated into the LL parent body (Choi et al, 1998), which suggests that the O‐isotopic composition of the nebular gas was spatially or temporally variable.     

Fayalitic olivine in CV3 chondrite matrix and dark inclusions: A nebular origin

Abstract— Fayalitic olivine (Fa₃₂) is the major component of the matrices and dark inclusions of CV3 and other unequilibrated chondrites. It occurs most commonly as rims, veins and halos in and around chondrule silicates in the Allende-type (CV3_OXA) chondrites and, to a much lesser extent, in the reduced (CV3R) and Bali-type (CV3OXB) chondrites. The olivines have distinctive platy, tabular and lath- or irregular-shaped crystals, with the ratio of the two types varying widely. In CV3_OXB chondrites, matrix fayalitic olivines range up to Fag_99.9; whereas, in the other CV3 chondrites, the range is much smaller. The platy and tabular anisotropic forms of the fayalitic olivines strongly suggest growth from a vapor, and the nature of the occurrences suggests that CV3 matrices are unequilibrated mixtures of nebular materials. We argue that the parent body hydration/dehydration model has numerous inconsistencies that make this hypothesis highly unlikely. These include: (1) There is no direct evidence linking fayalitic olivine to precursor phyllosilicates. (2) Dehydration of phyllosilicates cannot explain the wide range of morphologies of the fayalitic olivines. (3) Fayalitic olivine clearly predates the formation of the hydrous phases in CV3 chondrites and is one of the phases that breaks down to form phyllosilicates (Keller et al., 1994). (4) The unequilibrated nature of the matrix, including fine-scale zoning in 10 μm sized fayalitic olivine crystals, would not survive the parent body metamorphism required in the dehydration model. (5) A dark inclusion in the Ningqiang chondrite contains fayalitic olivine rimmed by glassy and microcrystalline material (Zolensky et al., 1997), which probably formed by radiation damage. This indicates that the fayalitic olivine was exposed to solar radiation in a nebular setting. (6) Some Allende chondrules contain unaltered primary, anhydrous glassy mesostasis in contact with the host matrix (e.g., Ikeda and Kimura, 1995). Chondrule mesostases would not have survived parent body hydration without becoming hydrated and would probably not survive the metamorphic heating required in the dehydration scenario. (7) Single platy and barrel-shaped crystals of fayalitic olivine are present in accretionary rims in calcium-aluminum-rich inclusions (CAIs) (MacPherson and Davis, 1997), which developed in the nebula. (8) Matrix lumps completely encased in chondrules in ordinary chondrites contain mainly fayalitic olivine (Scott et al., 1984), which indicates a nebular origin. (9) Oxygen isotopic compositions of Allende matrix and dark inclusions strongly indicate little or no hydration for Allende and its components (Clayton, 1997). We favor a nebular vaporization/recondensation model in which vaporization of chondritic dust produced a fayalite-rich vapor, followed by formation of the fayalitic olivine by direct recondensation from the vapor, epitactic growth on surfaces of existing forsterite and enstatite in chondrules, and replacement of existing forsterite and enstatite by gas-solid exchange.