Petrologic Type Research Articles

Mineral Composition and Structure of the Sverdlovsk Meteorite (H4-5)

A fragment of the Sverdlovsk Meteorite, which was found in 1985 in the Central Urals, is studied by modern analytical methods. It belongs to H chondrites of petrologic type 4–5; shock stage of meteorite is S1-2, terrestrial weathering is W1. The composition of minerals of the meteorite is studied. It is found for the first time that the metal and sulfides are concentrated in fine veinlets of the recrystallized matrix of the chondrite and are accompanied by segregations of metal and troilite inside these veinlets. The distribution of trace elements of the metal phase of the meteorite is studied.

Spectral evidence for amorphous silicates in least-processed CO meteorites and their parent bodies

Least-processed carbonaceous chondrites (carbonaceous chondrites that have experienced minimal aqueous alteration and thermal metamorphism) are characterized by their predominately amorphous iron-rich silicate interchondrule matrices and chondrule rims. This material is highly susceptible to destruction by the parent body processes of thermal metamorphism or aqueous alteration. The presence of abundant amorphous material in a meteorite indicates that the parent body, or at least a region of the parent body, experienced minimal processing since the time of accretion. The CO chemical group of carbonaceous chondrites has a significant number of these least-processed samples. We present visible/near-infrared and mid-infrared spectra of eight least-processed CO meteorites (petrologic type 3.0–3.1). In the visible/near-infrared, these COs are characterized by a broad weak feature that was first observed by Cloutis et al. (2012) to be at 1.3-µm and attributed to iron-rich amorphous silicate matrix materials. This feature is observed to be centered at 1.4-µm for terrestrially unweathered, least-processed CO meteorites. At mid-infrared wavelengths, a 21-µm feature, consistent with Si–O vibrations of amorphous materials and glasses, is also present. The spectral features of iron-rich amorphous silicate matrix are absent in both the near- and mid-infrared spectra of higher metamorphic grade COs because this material has recrystallized as crystalline olivine. Furthermore, spectra of least-processed primitive meteorites from other chemical groups (CRs, MET 00426 and QUE 99177, and C2-ungrouped Acfer 094), also exhibit a 21-µm feature. Thus, we conclude that the 1.4- and 21-µm features are characteristic of primitive least-processed meteorites from all chemical groups of carbonaceous chondrites. Finally, we present an IRTF + SPeX observation of asteroid (93) Minerva that has spectral similarities in the visible/near-infrared to the least-processed CO carbonaceous chondrites. While Minerva is not the only CO-like asteroid (e.g., Burbine et al., 2001), Minerva is likely the least-processed CO-like asteroid observed to date.

Petrology, phase equilibria modelling, noble gas chronology and thermal constraints of the El Pozo L5 meteorite

We present the results of physical properties, petrography, bulk chemistry, mineral compositions, phase relations modelling and Noble gases study of the meteorite El Pozo. The petrography and mineral compositions indicate that the meteorite is an L5 chondrite with a low shock stage of S2-S3. Heterogenous weathering was preferentially along shock structures. Thermobarometric calculations indicate thermal equilibrium conditions between 768 °C and 925 °C at ∼4 to 6 kb, which are substantially consistent with the petrological metamorphism type 5. A pseudosection phase diagram is relatively consistent with the mineral assemblage observed and PT conditions calculated. Temperature vs. fO2 diagram shows that plagioclase compositional stability is very sensitive to Tschermack substitution in orthopyroxene, clinopyroxene and XAn plagioclase during the high temperature metamorphic process. Based on noble gases He, Ne, Ar and K contents a cosmogenic exposure age CRE of 1.9 Myr was calculated. The 21Ne would be totally cosmogenic, with no primordial Ne. The 21Ne/22Ne value (0.97) is higher than solar value. According to the cosmogenic Ne content, we argue that El Pozo chondrite originally had a pre-atmospheric mass of 9–10 kg, which would have been produced by a later collision after the recognized collision of the L-chondrite parent body ∼470 Ma ago.

Chemical variations of sulfides and metal in enstatite chondrites—Introduction of a new classification scheme

AbstractIn this study, the metal and sulfide compositions of 45 enstatite chondrites were analyzed to determine possible mineral‐chemical trends correlated with the petrologic type. Data for 35 additional samples were taken from the literature. Considering the data from this huge number of different E chondrite samples (80 in total), none of the trends previously described in the literature could be clearly confirmed. Also, among the opaque phases of enstatite chondrites, no other “new” correlations between mineral chemistry and the petrologic type were found. However, major differences in the sulfide and metal chemistry became obvious. Specifically, a certain number of chondrites in the EH and the EL groups have Cr in troilite above 2 wt%, Fe in niningerite or alabandite above 20 wt%, and lack abundant daubréelite. Differences were also found for Ni concentrations in kamacite. Thus, we propose a system for classifying E chondrites by defining four major subgroups: EHa, ELa, EHb, and ELb. All subgroups show full petrologic sequences that are similar to each other. This observation, in combination with the differences in sulfide and metal chemistry, suggests an origin of the samples from different parent bodies. Considering the anomalous E chondrite samples that neither fit in the previous classification scheme nor in the new one described here, the samples investigated in this study require at least eight different parent bodies.

Origin of isotopically light nitrogen in meteorites

Bulk meteorite samples of various chemical classes and petrologic types (mainly carbonaceous chondrites) were systematically investigated by the stepped combustion method with the simultaneous isotopic analysis of carbon, nitrogen, and noble gases. A correlation was revealed between planetary noble gases associating with the Q phase and isotopically light nitrogen (δ15N up to –150‰). The analysis of this correlation showed that the isotopically light nitrogen (ILN) is carried by Q. In most meteorites, isotopically heavy nitrogen (IHN) of organic compounds (macromolecular material) is dominant. The ILN of presolar grains (diamond and SiC) and Q can be detected after separation from dominant IHN. Such a separation of nitrogen from Q and macromolecular material occurs under natural conditions and during laboratory stepped combustion owing to Q shielding from direct contact with oxygen, which results in Q oxidation at temperatures higher than the temperatures of the release of most IHN. There are arguments that ILN released at high temperature cannot be related to nanodiamond and SiC. The separation effect allowed us to constrain the contents of noble gases in Q, assuming that this phase is carbon-dominated. The directly measured 36Ar/C and 132Xe/C ratios in ILN-rich temperature fractions are up to 0.1 and 1 × 10–4 cm3/g, respectively. These are only lower constraints on the contents. The analysis of the obtained data on the three-isotope diagram δ15N–36Ar/14N showed that Q noble gases were lost to a large extent from most meteorites during the metamorphism of their parent bodies. Hence, the initial contents of noble gases in Q could be more than an order of magnitude higher than those directly measured. Compared with other carbon phases, Q was predominantly transformed to diamond in ureilites affected by shock metamorphism. The analysis of their Ar–N systematics showed that, similar to carbonaceous chondrites, noble gases were lost from Q probably before its transformation to diamond.

Halogens in chondritic meteorites and terrestrial accretion.

Volatile element delivery and retention played a fundamental part in Earth's formation and subsequent chemical differentiation. The heavy halogens-chlorine (Cl), bromine (Br) and iodine (I)-are key tracers of accretionary processes owing to their high volatility and incompatibility, but have low abundances in most geological and planetary materials. However, noble gas proxy isotopes produced during neutron irradiation provide a high-sensitivity tool for the determination of heavy halogen abundances. Using such isotopes, here we show that Cl, Br and I abundances in carbonaceous, enstatite, Rumuruti and primitive ordinary chondrites are about 6 times, 9 times and 15-37 times lower, respectively, than previously reported and usually accepted estimates. This is independent of the oxidation state or petrological type of the chondrites. The ratios Br/Cl and I/Cl in all studied chondrites show a limited range, indistinguishable from bulk silicate Earth estimates. Our results demonstrate that the halogen depletion of bulk silicate Earth relative to primitive meteorites is consistent with the depletion of lithophile elements of similar volatility. These results for carbonaceous chondrites reveal that late accretion, constrained to a maximum of 0.5 ± 0.2 per cent of Earth's silicate mass, cannot solely account for present-day terrestrial halogen inventories. It is estimated that 80-90 per cent of heavy halogens are concentrated in Earth's surface reservoirs and have not undergone the extreme early loss observed in atmosphere-forming elements. Therefore, in addition to late-stage terrestrial accretion of halogens and mantle degassing, which has removed less than half of Earth's dissolved mantle gases, the efficient extraction of halogen-rich fluids from the solid Earth during the earliest stages of terrestrial differentiation is also required to explain the presence of these heavy halogens at the surface. The hydropilic nature of halogens, whereby they track with water, supports this requirement, and is consistent with volatile-rich or water-rich late-stage terrestrial accretion.

Mineralogy and Surface Chemistry of Alberta Oil Sands: Relevance to Nonaqueous Solvent Bitumen Extraction

The mineralogy, chemistry, surface properties, and pore structure characteristics of the four different petrologic types of Alberta oil sands were determined in order to better understand their impact on nonaqueous solvent bitumen extraction. Quartz, clay minerals, and carbonates were the main mineral constituents of the studied samples. With increasing weight percentage of clay minerals, the solvent bitumen extraction (by the Dean–Stark procedure using toluene) decreased. Fine grained illite and illite-smectite had more detrimental effect on solvent bitumen extraction than coarse grained kaolinite. The pore structure data revealed that the extractability of bitumen from the oil sands depends on accessibility, more specifically on the size of bitumen-filled pores, by the solvent. The relative abundance and size of pores in the oil sands were controlled by mineral composition and particle size. Fine size fractions were typically enriched in kaolinite and 2:1 clay minerals (illite and illite-smectite) and c...

Intermineral oxygen three-isotope systematics of silicate minerals in equilibrated ordinary chondrites.

High precision oxygen three-isotope ratios were measured for four mineral phases (olivine, low-Ca and high-Ca pyroxene, and plagioclase) in equilibrated ordinary chondrites (EOC) using a secondary ion mass spectrometer. Eleven EOCs were studied that cover all groups (H, L, LL) and petrologic types (4, 5, 6), including S1-S4 shock stages, as well as unbrecciated and brecciated meteorites. SIMS analyses of multiple minerals were made in close proximity (mostly <100 μm) from several areas in each meteorite thin section, to evaluate isotope exchange among minerals. Oxygen isotope ratios in each mineral become more homogenized as petrologic type increases with the notable exception of brecciated samples. In type 4 chondrites, oxygen isotope ratios of olivine and low-Ca pyroxene are heterogeneous in both δ18O and Δ17O, showing similar systematics to those in type 3 chondrites. In types 5 and 6 chondrites, oxygen isotope ratios of the four mineral phases plot along mass dependent fractionation lines that are consistent with the bulk average Δ17O of each chondrite group. The δ18O of three minerals, low-Ca and high-Ca pyroxene and plagioclase, are consistent with equilibrium fractionation at temperatures of 700-1000°C. In most cases the δ18O values of olivine are higher than those expected from pyroxene and plagioclase, suggesting partial retention of premetamorphic values due to slower oxygen isotope diffusion in olivine than pyroxene during thermal metamorphism in ordinary chondrite parent bodies.

Trace element inventory of meteoritic Ca-phosphates

Most extraterrestrial samples feature the two accessory Ca-phosphates (apatite-group minerals and merrillite), which are important carrier phases of the rare earth elements (REE). The trace-element concentrations (REE, Sc, Ti, V, Cr, Mn, Co, As, Rb, Sr, Y, Zr, Nb, Ba, Hf, Ta, Pb, Th, and U) of selected grains were analyzed by LA-ICP-MS and/or SIMS (REE only). This systematic investigation includes 99 apatite and 149 merrillite analyses from meteorites deriving from various asteroidal bodies including 1 carbonaceous chondrite, 8 ordinary chondrites, 3 acapulcoites, 1 winonaite, 2 eucrites, 5 shergottites, 1 ureilitic trachyandesite, 2 mesosiderites, and 1 silicate-bearing IAB iron meteorite. Although Ca-phosphates predominantly form in metamorphic and/or metasomatic reactions, some are of igneous origin. As late-stage phases that often incorporate the vast majority of their host’s bulk REE budget, the investigated Ca-phosphates have REE enrichments of up to two orders of magnitude compared to the host rock’s bulk concentrations. Within a single sample, each phosphate species displays a uniform REE-pattern, and variations are mainly restricted to their enrichment, therefore indicating similar formation conditions. Exceptions are brecciated samples, i.e., the Adzhi-Bogdo (LL3-6) ordinary chondrite. Despite this uniformity within single samples, distinct meteorite groups do not necessarily have unique REE-patterns. Four basic shapes dominate the REE patterns of meteoritic Ca-phosphates: (1) flat patterns, smoothly decreasing from La-Lu with prominent negative Eu anomalies (acapulcoites, eucrites, apatite from the winonaite and the ureilitic trachyandesite, merrillite from ordinary chondrites); (2) unfractionated patterns, with only minor or no anomalies (mesosiderites, enriched shergottites, IAB-iron meteorite); (3) LREE-enriched patterns, with either positive or slightly negative Eu anomalies (chondritic apatite); and (4) strongly LREE-depleted patterns, with negative Eu anomalies (depleted shergottites). The patterns do not correlate with the grade of metamorphism (petrologic type), specific adjacent mineral assemblages or with Ca-phosphate grain size. Neither the proportions of different REE, nor particular REE patterns themselves are universally correlated to a specific formation mechanism yet Eu (i.e., magnitude of the Eu anomaly) is a sensitive indicator to evaluate the timing of plagioclase and phosphate crystallization. Based on our data, U and Th abundances in apatite increase (almost linearly) with the grade of metamorphism, as well as with the differentiation of their host rock.

Reclassification of Hart and Northwest Africa 6047: Criteria for distinguishing between CV and CK3 chondrites

AbstractThe single parent body model for the CV and CK chondrites (Greenwood et al. ) was challenged by Dunn et al. (), who argued that magnetite compositions could not be reconciled by a single metamorphic sequence (i.e., CV3 → CK3 → CK4–6). Cr isotopic compositions, which are distinguishable between the CV and CK chondrites, also support two different parent bodies (Yin et al. ). Despite this, there are many petrographic and mineralogical similarities between the unequilibrated (petrologic type 3) CK chondrites and the CV chondrites (also type 3), which may result in misclassification of samples. Hart and Northwest Africa 6047 (NWA 6047) are an excellent example of this. In this study, we revisit the classification of Hart and NWA 6047 using magnetite compositions, petrography, and compositions of olivine, the most ubiquitous mineral in both CV and CK chondrites. Not only do our results suggest that NWA 6047 and Hart were misclassified, but our assessment of CV and CK3 chondrites has also led to the development of criteria that can be used to distinguish between CV and CK3 chondrites. These criteria include: abundances of Cr2O3, TiO2, NiO, and Al2O3 in magnetite; Fa content and NiO abundance of matrix olivine; FeO content of chondrules; and the chondrule:matrix ratio. Classification as a CV chondrite is also supported by the presence of igneous chondrule rims, calcium‐aluminum‐rich inclusions, and an elongated petrofabric. However, none of these petrographic characteristics can be used conclusively to distinguish between CV and CK3 chondrites.

CORRELATIONS BETWEEN PHYSICAL PROPERTIES AND POINT LOAD STRENGTH INDEX OF PRASINITES: A CASE STUDY FROM EAST ATTICA PREFECTURE

The aim of this study is to investigate the statistical correlations between the point load strength index and certain physical properties, e.g. the dry density and the dry longitudinal ultrasonic wave velocity of prasinites (metabasites). Statistically significant correlations established between the physical properties as well as between each physical quantity and the point load strength index. According to bibliography, this is one of the first efforts to develop relations between physical and mechanical properties for this particular petrological type, and therefore the derived equations can be a useful tool to the investigation of these petrological types, either in the study area or in other sites, where prasinites of similar structural characteristics, are examined for the foundation of various constructions.

Magnesium isotope systematics in Martian meteorites

Magnesium isotope compositions are reported for a suite of Martian meteorites that span the range of petrological and geochemical types recognized to date for Mars, including crustal breccia Northwest Africa (NWA) 7034. The δ26Mg values (per mil units relative to DSM-3 reference material) range from −0.32 to −0.11‰; basaltic shergottites and nakhlites lie to the heavier end of the Mg isotope range whereas olivine-phyric, olivine–orthopyroxene-phyric and lherzolitic shergottites, and chassignites have slightly lighter Mg isotope compositions, attesting to modest correlation of Mg isotopes and petrology of the samples. Slightly heavier Mg isotope compositions found for surface-related materials (NWA 7034, black glass fraction of the Tissint shergottite fall; δ26Mg > −0.17‰) indicate measurable Mg isotope difference between the Martian mantle and crust but the true extent of Mg isotope fractionation for Martian surface materials remains unconstrained. The range of δ26Mg values from −0.19 to −0.11‰ in nakhlites is most likely due to accumulation of clinopyroxene during petrogenesis rather than garnet fractionation in the source or assimilation of surface material modified at low temperatures. The rather restricted range in Mg isotope compositions between spatially and temporally distinct mantle-derived samples supports the idea of inefficient/absent major tectonic cycles on Mars, which would include plate tectonics and large-scale recycling of isotopically fractionated surface materials back into the Martian mantle. The cumulative δ26Mg value of Martian samples, which are not influenced by late-stage alteration processes and/or crust–mantle interactions, is −0.271±0.040‰ (2SD) and is considered to reflect δ26Mg value of the Bulk Silicate Mars. This value is robust taking into account the range of lithologies involved in this estimate. It also attests to the lack of the Mg isotope variability reported for the inner Solar System bodies at current analytical precision, also noted for several other major elements.

Petrography, classification, oxygen isotopes, noble gases, and cosmogenic records of Kamargaon (L6) meteorite: The latest fall in India

AbstractA single piece of meteorite fell on Kamargaon village in the state of Assam in India on November 13, 2015. Based on mineralogical, chemical, and oxygen isotope data, Kamargaon is classified as an L‐chondrite. Homogeneous olivine (Fa: 25 ± 0.7) and low‐Ca pyroxene (Fs: 21 ± 0.4) compositions with percent mean deviation of &lt;2, further suggest that Kamargaon is a coarsely equilibrated, petrologic type 6 chondrite. Kamargaon is thermally metamorphosed with an estimated peak metamorphic temperature of ~800 °C as determined by two‐pyroxene thermometry. Shock metamorphism studies suggest that this meteorite include portions of different shock stages, e.g., S3 and S4 (Stöffler et al. ); however, local presence of quenched metal‐sulfide melt within shock veins/pockets suggest disequilibrium melting and relatively higher shock stage of up to S5 (Bennett and McSween ). Based on noble gas isotopes, the cosmic‐ray exposure age is estimated as 7.03 ± 1.60 Ma and nitrogen isotope composition (δ15N = 18‰) also correspond well with the L‐chondrite group. The He‐U, Th, and K‐Ar yield younger ages (170 ± 25 Ma 684 ± 93, respectively) and are discordant. A loss of He during the resetting event is implied by the lower He‐U and Th age. Elemental ratios of trapped Ar, Kr, and Xe can be explained through the presence of a normal Q noble gas component. Relatively low activity of 26Al (39 dpm/kg) and the absence of 60Co activity suggest a likely low shielding depth and envisage a small preatmospheric size of the meteoroid (&lt;10 cm in radius). The Kr isotopic ratios (82Kr/84Kr) further argue that the meteorite was derived from a shallow depth.

Characterizing amorphous silicates in extraterrestrial materials: Polymerization effects on Raman and mid‐IR spectral features of alkali and alkali earth silicate glasses

AbstractAmorphous silicates are common in extraterrestrial materials, especially in carbonaceous chondrites of petrologic types 1 and 2. In addition, high percentage of amorphous components and poorly crystalline phyllosilicates were found in the mudstones at Gale Crater by the CheMin instruments on board of Mar Curiosity rover, which illustrates the importance of characterizing amorphous silicates in future planetary surface explorations. The structure of an amorphous silicate can vary in two aspects: the degree of polymerization and the degree of crystallinity. Here we present the first phase study on characterizing synthetic alkali and alkali earth silicate glasses with different degrees of polymerization by using vibration spectroscopy. Compared with crystalline silicates, their Raman and mid‐IR spectra show broad spectral peaks but have the similar peak positions. We find that a change in the degree of polymerization of these silicate glasses affects their Raman band positions, especially the ratio of Raman band intensities, as well as the positions of the Christiansen feature and reststrahlen bands in their mid‐IR absorbance spectra. Based on these observations, we establish a calibration curve that could enable semiquantification of the polymerization degree of silicate glasses in planetary surface/subsurface materials during future robotic planetary surface exploration missions.

Diffusion of Oxygen Isotopes in Thermally Evolving Planetesimals and Size Ranges of Presolar Silicate Grains

Abstract Presolar grains are small particles found in meteorites through their isotopic compositions, which are considerably different from those of materials in the solar system. If some isotopes in presolar grains diffused out beyond their grain sizes when they were embedded in parent bodies of meteorites, their isotopic compositions could be washed out, and hence the grains could no longer be identified as presolar grains. We explore this possibility for the first time by self-consistently simulating the thermal evolution of planetesimals and the diffusion length of 18O in presolar silicate grains. Our results show that presolar silicate grains smaller than ∼0.03 μm cannot keep their original isotopic compositions even if the host planetesimals experienced a maximum temperature as low as 600 °C. Since this temperature corresponds to that experienced by petrologic type 3 chondrites, isotopic diffusion can constrain the size of presolar silicate grains discovered in such chondrites to be larger than ∼0.03 μm. We also find that the diffusion length of 18O reaches ∼0.3–2 μm in planetesimals that were heated up to 700–800°C. This indicates that, if the original size of presolar grains spans a range from ∼0.001 μm to ∼0.3 μm like that in the interstellar medium, then the isotopic records of the presolar grains may be almost completely lost in such highly thermalized parent bodies. We propose that isotopic diffusion could be a key process to control the size distribution and abundance of presolar grains in some types of chondrites.

The accretion and impact history of the ordinary chondrite parent bodies

A working timeline for the history of ordinary chondrites includes chondrule formation as early as 0–2Ma after our Solar System’s earliest forming solids (CAIs), followed by rapid accretion into undifferentiated planetesimals that were heated internally by 26Al decay and cooled over a period of tens of millions of years. There remains conflict, however, between metallographic cooling rate (Ni-metal) and radioisotopic thermochronometric data over the sizes and lifetimes of the chondrite parent bodies, as well as the timing of impact related disruptions. The importance of establishing the timing of parent body disruption is heightened by the use of meteorites as recorders of asteroid belt wide disruption events and their use to interpret Solar System dynamical models. Here we attempt to resolve these records by contributing new 207Pb–206Pb data obtained on phosphates isolated from nine previously unstudied ordinary chondrites. These new results, along with previously published Pb-phosphate, Ni-metal and thermometry data, are interpreted with a series of numerical models designed to simulate the thermal evolution for a chondrite parent body that either remains intact or is disrupted by impact prior to forming smaller unsorted “rubble piles”.Our thermal model and previously published thermometry data limit accretion time to 2.05–2.25Ma after CAIs. Measured Pb-phosphate data place minimum estimates on parent body diameters of ∼260–280km for both the L and H chondrite parent bodies. They also consistently show that petrologic Type 6 (highest thermal metamorphism) chondrites from both the H and L bodies have younger ages and, therefore, cooled more slowly than Type 5 (lesser metamorphism) chondrites. This is interpreted as evidence for Type 5 chondrite origination from shallower depths than Type 6 chondrites within initially concentrically zoned bodies. This contrasts metallographic cooling rate data that are inconsistent with such a simple onion shell scenario. One model that can reconcile these two data sets takes into account subtle differences in temperature to which each system responds. This working model requires that disruption occur early enough such that the Ni-metal system can record the cooling rate associated with a rubble pile (<70Ma), yet late enough that the Pb-phosphate system can record an onion shell structure (>30Ma). For this 30–70Ma timeline, reaccretion into smaller rubble piles will ensure that the originally deeply buried and hot Type 6 samples will always cool faster as a result of disruption, yielding nearly uniform ages that record the time of parent body disruption. This is consistent with the available Pb-phosphate data, where all but one Type 6 chondrite (H, n=3; L, n=4) yields a cooling age within a narrow 4505±5Ma timeframe. These data collectively imply that both the H and L chondrite parent bodies were catastrophically disrupted at ∼60Ma. In addition, combined Ni-metal and Pb-phosphate models confirm that a subset of Type 4 chondrites record early rapid cooling likely associated with erosional impacting of the H and L parent bodies on ∼5Ma timescales.

The Ozernoye meteorite: New data on mineralogy

New data on the mineral composition of the Ozernoye meteorite, found in the Kurgan region in 1983, are presented. It has been found that that the meteorite’s matter is composed of olivine (chrysolite), orthopyroxene (bronzite), clinopyroxene (augite), maskelynite, chromite, ilmenite, metals Fe and Ni (kamasite, taenite), sulfides (troilite, pentlandite), chlorapatite, and merrillite. Augite, taenite, pentlandite, and merrillite were identified in the Ozernoye meteorite for the first time. The chemical compositions are given for all these minerals. The meteorite itself is an ordinary chondrite stone belonging to petrological type L5.

Phosphate minerals in the H group of ordinary chondrites, and fluid activity recorded by apatite heterogeneity in the Zag H3-6 regolith breccia

Phosphate minerals in ordinary chondrites provide a record of fluids that were present during metamorphic heating of the chondrite parent asteroids. We have carried out a petrographic study of the phosphate minerals, merrillite and apatite, in metamorphosed H group ordinary chondrites of petrologic type 4–6, to understand development of phosphate minerals and associated fluid evolution during metamorphism. In unbrecciated chondrites, apatite is Cl rich and shows textural evolution from fine-grained apatite-merrillite assemblages in type 4 toward larger, uniform grains in type 6. The Cl/F ratio in apatite shows a similar degree of heterogeneity in all petrologic types, and no systematic change in compositions with metamorphic grade, which suggests that compositions in each meteorite are dictated by localized conditions, possibly because of a limited fluid/rock ratio. The development of phosphate minerals in H chondrites is similar to that of L and LL chondrites, despite the fact that feldspar equilibration resulting from albitization is complete in H4 chondrites but not in L4 or LL4 chondrites. This suggests that albitization took place during an earlier period of the metamorphic history than that recorded by preserved apatite compositions, and chemical equilibrium was not achieved throughout the H chondrite parent body or bodies during the late stages of metamorphism. A relict igneous clast in the H5 chondrite, Oro Grande has apatite rims on relict phenocrysts of (possibly) diopside that have equilibrated with the host chondrite. Apatite in the Zag H3–6 regolith breccia records a complex fluid history, which is likely related to the presence of halite in this meteorite. The porous dark H4 matrix of Zag, where halite is observed, has a high apatite/merrillite ratio, and apatite is extremely Cl rich. One light H6 clast contains similarly Cl-rich apatite. In a second light H6 clast, apatite compositions are very heterogeneous and more F-rich. Apatites in both H4 matrix and H6 clasts have very low H_2O contents. Heterogeneous apatite compositions in Zag record multiple stages of regolith processing and shock at the surface of the H chondrite parent body, and apatite records either the passage of fluids of variable compositions resulting from different impact-related processes, or the passage of a single fluid whose composition evolved as it interacted with the chondrite regolith. Unraveling the history of apatite can potentially help to interpret the internal structure of chondrite parent bodies, with implications for physical and mechanical properties of chondritic asteroids. The behavior of halogens recorded by apatite is important for understanding the behavior of volatile elements in general: if impact-melt materials close to the surface of a chondritic asteroid are readily degassed, the volatile inventories of terrestrial planets could be considerably more depleted than the CI carbonaceous chondrite abundances that are commonly assumed.

Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies

AbstractIn ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent‐body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4–6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all threeOCgroups. Apatite in L chondrites is Cl‐rich, similar to H chondrites, whereas apatite inLLchondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend toLLchondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4–6. Alkali‐ and halogen‐rich and likely hydrous metasomatic fluids acted during prograde metamorphism onOCparent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl‐rich composition after the asteroid began to cool. Differences in secondary minerals between H and L,LLchondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology‐dependent apatite compositions. Bulk Cl/F ratios forOCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios inOCs are similar toCI.

Why is it so difficult to classify Renazzo-type (CR) carbonaceous chondrites? – Implications from TEM observations of matrices for the sequences of aqueous alteration

A number of different classifications have been proposed for the CR chondrites; this study aims at reconciling these different schemes. Mineralogy-based classification has proved particularly challenging for weakly to moderately altered CRs because incipient mineral replacement and elemental mobilization arising from aqueous alteration only affected the most susceptible primary phases, which are generally located in the matrix. Secondary matrix phases are extremely fine-grained (generally sub-micron) and heterogeneously mixed with primary nebular materials. Compositional and isotopic classification parameters are fraught with confounding factors, such as terrestrial weathering, impact processes, and variable abundance of clasts from different regions of the CR parent body or from altogether different planetary bodies. Here, detailed TEM observations from eighteen FIB sections retrieved from the matrices of nine Antarctic CR chondrites (EET 96259, GRA 95229, GRO 95577, GRO 03116, LAP 02342, LAP 04516, LAP 04720, MIL 07525, and MIL 090001) are presented, representing a range of petrologic types. Amorphous Fe–Mg silicates are found to be the dominant phase in all but the most altered CR chondrite matrices, which still retain significant amounts of these amorphous materials. Amorphous Fe–Mg silicates are mixed with phyllosilicates at the nanometer scale. The ratio of amorphous Fe–Mg silicates to phyllosilicates decreases as: (1) the size of phyllosilicates, (2) abundance of magnetite, and (3) replacement of Fe–Ni sulfides increase. Carbonates are only abundant in the most altered CR chondrite, GRO 95577. Nanophase Fe–Ni metal and tochilinite are present small abundances in most CR matrices. Based on the presence, abundance and size of phyllosilicates with respect to amorphous Fe–Mg silicates, the sub-micron features of CR chondrites have been linked to existing classification sequences, and possible reasons for inconsistencies among classification schemes are discussed.