Ordinary chondrite metallography: Part 2. Formation of zoned and unzoned metal particles in relatively unshocked H,L, and LL chondrites

Abstract— We studied the metallography of Fe‐Ni metal particles in 17 relatively unshocked ordinary chondrites and interpreted their microstructures using the results of P‐free, Fe‐Ni alloy cooling experiments (described in Reisener and Goldstein 2003). Two types of Fe‐Ni metal particles were observed in the chondrites: zoned taenite + kamacite particles and zoneless plessite particles, which lack systematic Ni zoning and consist of tetrataenite in a kamacite matrix. Both types of metal particles formed during metamorphism in a parent body from homogeneous, P‐poor taenite grains. The phase transformations during cooling from peak metamorphic temperatures were controlled by the presence or absence of grain boundaries in the taenite particles. Polycrystalline taenite particles transformed to zoned taenite + kamacite particles by kamacite nucleation at taenite/taenite grain boundaries during cooling. Monocrystalline taenite particles transformed to zoneless plessite particles by martensite formation and subsequent martensite decomposition to tetrataenite and kamacite during the same cooling process. The varying proportions of zoned taenite + kamacite particles and zoneless plessite particles in types 4–6 ordinary chondrites can be attributed to the conversion of polycrystalline taenite to monocrystalline taenite during metamorphism. Type 4 chondrites have no zoneless plessite particles because metamorphism was not intense enough to form monocrystalline taenite particles. Type 6 chondrites have larger and more abundant zoneless plessite particles than type 5 chondrites because intense metamorphism in type 6 chondrites generated more monocrystalline taenite particles. The distribution of zoneless plessite particles in ordinary chondrites is entirely consistent with our understanding of Fe‐Ni alloy phase transformations during cooling. The distribution cannot be explained by hot accretion‐autometamorphism, post‐metamorphic brecciation, or shock processing.     

Low‐temperature phase decomposition in iron‐nickel metal of the Portales Valley meteorite

Abstract— The Portales Valley meteorite provides an opportunity to investigate and compare the microstructure in Fe‐Ni metal of the metallic particles in the chondritic portion and in the metal veins. The low‐temperature phase decomposition of Fe‐Ni metal was investigated using scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. The microstructure is formed as the Portales Valley meteorite cooled from high temperatures and includes the outer taenite rim, the cloudy zone, clear taenite, and martensite. Martensite in turn decomposes into a fine admixture of fcc rods in a bcc matrix. The width of the island phase of the cloudy zone in the metal particles of the chondritic portion and the metal veins can be used to estimate a low‐temperature cooling rate. The microstructural evidence indicates that the chondritic portions and the metal veins in the Portales Valley meteorite cooled together as a mixture with a cooling rate of roughly 6.5 K/Ma.     

Mineralogy,petrography, and thermometry of the H5 chondrite Carcote,Chile

Abstract— The Carcote meteorite, detected in 1888 in the northern Chilean Andes, is a brecciated, weakly shocked H5 chondrite. It contains a few barred olivine chondrules and, even more rarely, fan-shaped or granular orthopyroxene chondrules. The chondrules are situated in a fine-grained matrix that consists predominantly of olivine and orthopyroxene with accessory clinopyroxene, troilite, chromite, merrillite, and plagioclase. The metal phase is mainly kamacite with subordinate taenite and traces of native Cu. In its bulk rock composition, Carcote compares well with other H5 chondrites so far analysed, except for a distinctly higher C content. Microprobe analyses revealed the following mineral compositions: olivine (Fa_16.5–20), orthopyroxene (Fs_14–17.5), diopsidic clinopyroxene (FS_6–7), plagioclase (An_15–20). Troilite is stoichimetric FeS with traces of Ni and Cr; chromite has Cr/(Cr + Al) of 0.86, Fe²⁺/(Fe²⁺ + Mg) of 0.80-0.88 and contains considerable amounts of Ti, Mn, and Zn. Merrillite is close to the theoretical formula Ca₁₈(Mg, Fe)₂Na₂(PO₄)₁₄, although with a Na deficiency not compensated for by excess Ca; the Mg/(Mg + Fe²⁺) ratio of the Carcote merrilite is 0.93-0.95. Kamacite and taenite have Ni contents of 5.6–7.2 and 17.1–23.4 wt%, respectively. Native Cu contains about 3.1–3.3 wt% Fe and 1.6 wt% Ni. Application of different geothermometers to the Carcote H5 chondrite yielded apparently inconsistent results. The highest temperature range of 850–950 °C (at 1 bar) is derived from the Ca-in-opx thermometer. From the cpx-opx solvus geothermometers and the two-pyroxene Fe-Mg exchange geothermometer, a lower temperature range of 750–840 °C is estimated, whereas lower and more variable temperatures of 630–770 °C are obtained from the Ca-in-olivine geothermometer. Recent calibrations of the olivine-spinel geothermometer yielded a still lower temperature range of 570–670 °C, which fits well to the temperature information derived from the Ni distribution between kamacite and taenite. Judging from crystal chemical considerations, we assume that these different temperatures reflect the closure of different exchange equilibria during cooling of the meteorite parent body.     

Ordinary chondrite metallography: Part 1. Fe‐Ni taenite cooling experiments

Abstract— Cooling rate experiments were performed on P‐free Fe‐Ni alloys that are compositionally similar to ordinary chondrite metal to study the taenite ? taenite + kamacite reaction. The role of taenite grain boundaries and the effect of adding Co and S to Fe‐Ni alloys were investigated. In P‐free alloys, kamacite nucleates at taenite/taenite grain boundaries, taenite triple junctions, and taenite grain corners. Grain boundary diffusion enables growth of kamacite grain boundary precipitates into one of the parent taenite grains. Likely, grain boundary nucleation and grain boundary diffusion are the applicable mechanisms for the development of the microstructure of much of the metal in ordinary chondrites. No intragranular (matrix) kamacite precipitates are observed in P‐free Fe‐Ni alloys. The absence of intragranular kamacite indicates that P‐free, monocrystalline taenite particles will transform to martensite upon cooling. This transformation process could explain the metallography of zoneless plessite particles observed in H and L chondrites. In P‐bearing Fe‐Ni alloys and iron meteorites, kamacite precipitates can nucleate both on taenite grain boundaries and intragranularly as Widmanstätten kamacite plates. Therefore, P‐free chondritic metal and P‐bearing iron meteorite/pallasite metal are controlled by different chemical systems and different types of taenite transformation processes.     

Rumanová H5 chondrite,Slovaki

Abstract— An H5 chondrite was found near the village of Rumanová, Slovakia. dominant minerals of the meteorite are enstatite, olivine, kamacite, taenite and troilite. The minor minerals are oligoclase, augite, pigeonite, accessory chromite, whitlockite and chlorapatite. The composition of olivine (Fa_19.0) and low-Ca orthopyroxene (Fs_17.0), and the density and chemical composition of the meteorite correspond to those of an H chondrite. Normal zoning of Ni in metal grains and parallel planar fractures in olivine suggest weak shock metamorphism of stage S3. Due to moderate oxidation of metal, iron hydroxides were formed corresponding to weathering stage W2.     

Cooling rates of porphyritic olivine chondrules in the Semarkona (LL3.00) ordinary chondrite: A model for diffusional equilibration of olivine during fractional crystallization

Abstract— Cooling rates of chondrules provide important constraints on the formation process of chondrite components at high temperatures. Although many dynamic crystallization experiments have been performed to obtain the cooling rate of chondrules, these only provide a possible range of cooling rates, rather than providing actual measured values from natural chondrules. We have developed a new model to calculate chondrule cooling rates by using the Fe‐Mg chemical zoning profile of olivine, considering diffusional modification of zoning profiles as crystals grow by fractional crystallization from a chondrule melt. The model was successfully verified by reproducing the Fe‐Mg zoning profiles obtained in dynamic crystallization experiments on analogs for type II chondrules in Semarkona. We applied the model to calculating cooling rates for olivine grains of type II porphyritic olivine chondrules in the Semarkona (LL3.00) ordinary chondrite. Calculated cooling rates show a wide range from 0.7 °C/h to 2400 °C/h and are broadly consistent with those obtained by dynamic crystallization experiments (10–1000 °C/h). Variations in cooling rates in individual chondrules can be attributed to the fact that we modeled grains with different core Fa compositions that are more Fe‐rich either because of sectioning effects or because of delayed nucleation. Variations in cooling rates among chondrules suggest that each chondrule formed in different conditions, for example in regions with varying gas density, and assembled in the Semarkona parent body after chondrule formation.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

On the lower limit of chondrule cooling rates: The significance of iron loss in dynamic crystallization experiments

Abstract— Dynamic crystallization experiments performed with different container materials (Fe crucible, pure Pt wire loop, presaturated Pt wire loop) demonstrate the strong influence of Fe loss on texture, mineralogy and chemical zoning in olivine. The use of pure Pt wire loops results in severe Fe loss and prevents the development of strong Fe/Mg zoning in olivine in slower cooled runs (≤ 100 °C/h). Presaturated Pt wire loops reduce Fe loss to some extent but not completely. If severe Fe loss from the melt is avoided by the use of Fe crucibles, then cooling rates between 2000 and 1.2 °C/h yield textures, modal mineral abundances and Fe/Mg zoning in olivine comparable to natural porphyritic olivine chondrules. However, Fe gain from the crucible may possibly enhance Fe/Mg zoning in olivine for cooling rates < 10 °C/h. Therefore, it is concluded that the lower limit of cooling rates of porphyritic olivine chondrules derived from dynamic crystallization experiments is 10 °C/h, perhaps it is even lower, on the order of a few degrees Celsius per hour. This value is not significantly different from estimates for subsolidus temperatures based on the microstructure of chondrule minerals (Weinbruch and Müller, 1995). The lower limit of chondrule cooling rates of 100 °C/h advocated by Hewins (1988) and Radomsky and Hewins (1990) seems to be an artifact of the experimental technique, as their samples were crystallized in pure Pt wire loops.     

What metal‐troilite textures can tell us about post‐impact metamorphism in chondrite meteorites

Abstract— Metal‐troilite textures are examined in metamorphosed and impact‐affected ordinary chondrites to examine the response of these phases to rapid changes in temperature. Complexly intergrown metal‐troilite textures are shown to form in response to three different impact‐related processes. (1) During impacts, immiscible melt emulsions form in response to spatially focused heating. (2) Immediately after impact events, re‐equilibration of heterogeneously distributed heat promotes metamorphism adjacent to zones of maximum impact heating. Where temperatures exceed ～850 ° C, this post‐impact metamorphism results in melting of conjoined metal‐troilite grains in chondrites that were previously equilibrated through radiogenic metamorphism. When the resulting Fe‐Ni‐S melt domains crystallize, a finely intergrown mixture of troilite and metal forms, which can be zoned with kamacite‐rich margins and taenite‐rich cores. (3) At lower temperatures, post‐impact metamorphism can also cause liberation of sulfur from troilite, which migrates into adjacent Fe‐Ni metal, allowing formation of troilite and occasionally copper within the metal during cooling. Because impact events cause heating within a small volume, post‐impact metamorphism is a short duration event (days to years) compared with radiogenic metamorphism (>10⁶ years). The fast kinetics of metal‐sulfide reactions allows widespread textural changes in conjoined metal‐troilite grains during post‐impact metamorphism, whereas the slow rate of silicate reactions causes these to be either unaffected or only partially annealed, except in the largest impact events. Utilizing this knowledge, information can be gleaned as to whether a given meteorite has suffered a post‐impact thermal overprint, and some constraints can be placed on the temperatures reached and duration of heating.     

Minor and trace element concentrations in adjacent kamacite and taenite in the Krymka chondrite

We report in situ NanoSIMS siderophile minor and trace element abundances in individual Fe‐Ni metal grains in the unequilibrated chondrite Krymka (LL3.2). Associated kamacite and taenite of 10 metal grains in four chondrules and one matrix metal were analyzed for elemental concentrations of Fe, Ni, Co, Cu, Rh, Ir, and Pt. The results show large elemental variations among the metal grains. However, complementary and correlative variations exist between adjacent kamacite‐taenite. This is consistent with the unequilibrated character of the chondrite and corroborates an attainment of chemical equilibrium between the metal phases. The calculated equilibrium temperature is 446 ± 9 °C. This is concordant with the range given by Kimura et al. (2008) for the Krymka postaccretion thermal metamorphism. Based on Ni diffusivity in taenite, a slow cooling rate is estimated of the Krymka parent body that does not exceed ~1K Myr^?1, which is consistent with cooling rates inferred by other workers for unequilibrated ordinary chondrites. Elemental ionic radii might have played a role in controlling elemental partitioning between kamacite and taenite. The bulk compositions of the Krymka metal grains have nonsolar (mostly subsolar) element/Ni ratios suggesting the Fe‐Ni grains could have formed from distinct precursors of nonsolar compositions or had their compositions modified subsequent to chondrule formation events.     

Heavily metamorphosed clasts from the CV chondrite breccias Mokoia and Yamato‐86009

Abstract– Metamorphosed clasts in the CV carbonaceous chondrite breccias Mokoia and Yamato‐86009 (Y‐86009) are coarse‐grained, granular, polymineralic rocks composed of Ca‐bearing (up to 0.6 wt% CaO) ferroan olivine (Fa_34–39), ferroan Al‐diopside (Fs_9–13Wo_47–50, approximately 2–7 wt% Al₂O₃), plagioclase (An_37–84Ab_63–17), Cr‐spinel (Cr/(Cr + Al) = 0.19–0.45, Fe/(Fe + Mg) = 0.60–0.79), nepheline, pyrrhotite, pentlandite, Ca‐phosphate, and rare grains of Ni‐rich taenite; low‐Ca pyroxene is absent. Most clasts have triple junctions between silicate grains, indicative of prolonged thermal annealing. Based on the olivine‐spinel and pyroxene thermometry, the estimated metamorphic temperature recorded by the clasts is approximately 1100 K. Few clasts experienced thermal metamorphism to a lower degree and preserved chondrule‐like textures. The Mokoia and Y‐86009 clasts are mineralogically unique and different from metamorphosed chondrites of known groups (H, L, LL, R, EH, EL, CO, CK) and primitive achondrites (acapulcoites, brachinites, lodranites). On a three‐isotope oxygen diagram, compositions of olivine in the clasts plot along carbonaceous chondrite anhydrous mineral line and the Allende mass‐fractionation line, and overlap with those of the CV chondrule olivines; the Δ¹⁷O values of the clasts range from about ?4.3‰ to ?3.0‰. We suggest that the clasts represent fragments of the CV‐like material that experienced metasomatic alteration, high‐temperature metamorphism, and possibly melting in the interior of the CV parent asteroid. The lack of low‐Ca pyroxene in the clasts could be due to its replacement by ferroan olivine during iron‐alkali metasomatic alteration or by high‐Ca ferroan pyroxene during melting under oxidizing conditions.     

Ferrous silicate spherules with euhedral iron‐nickel metal grains from CH carbonaceous chondrites: Evidence for supercooling and condensation under oxidizing conditions

Abstract— The CH carbonaceous chondrites contain a population of ferrous (Fe/(Fe + Mg) ? 0.1‐0.4) silicate spherules (chondrules), about 15–30 μm in apparent diameter, composed of cryptocrystalline olivinepyroxene normative material, ±SiO₂‐rich glass, and rounded‐to‐euhedral Fe, Ni metal grains. The silicate portions of the spherules are highly depleted in refractory lithophile elements (CaO, Al₂O₃, and TiO₂ <0.04 wt%) and enriched in FeO, MnO, Cr₂O₃, and Na₂O relative to the dominant, volatile‐poor, magnesian chondrules from CH chondrites. The Fe/(Fe + Mg) ratio in the silicate portions of the spherules is positively correlated with Fe concentration in metal grains, which suggests that this correlation is not due to oxidation, reduction, or both of iron (FeO_sil ? Fe_met) during melting of metal‐silicate solid precursors. Rather, we suggest that this is a condensation signature of the precursors formed under oxidizing conditions. Each metal grain is compositionally uniform, but there are significant intergrain compositional variations: about 8–18 wt% Ni, <0.09 wt% Cr, and a sub‐solar Co/Ni ratio. The precursor materials of these spherules were thus characterized by extreme elemental fractionations, which have not been observed in chondritic materials before. Particularly striking is the fractionation of Ni and Co in the rounded‐to‐euhedral metal grains, which has resulted in a Co/Ni ratio significantly below solar. The liquidus temperatures of the euhedral Fe, Ni metal grains are lower than those of the coexisting ferrous silicates, and we infer that the former crystallized in supercooled silicate melts. The metal grains are compositionally metastable; they are not decomposed into taenite and kamacite, which suggests fast postcrystallization cooling at temperatures below 970 K and lack of subsequent prolonged thermal metamorphism at temperatures above 400–500 K.     

Restriction of parent body heating by metal‐troilite melting: Thermal models for the ordinary chondrites

Ordinary chondrite meteorites contain silicates, Fe,Ni‐metal grains, and troilite (FeS). Conjoined metal‐troilite grains would be the first phase to melt during radiogenic heating in the parent body, if temperatures reached over approximately 910–960 °C (the Fe,Ni‐FeS eutectic). On the basis of two‐pyroxene thermometry of 13 ordinary chondrites, we argue that peak temperatures in some type 6 chondrites exceeded the Fe,Ni‐FeS eutectic and thus conjoined metal‐troilite grains would have begun to melt. Melting reactions consume energy, so thermal models were constructed to investigate the effect of melting on the thermal history of the H, L, and LL parent asteroids. We constrained the models by finding the proportions of conjoined metal‐troilite grains in ordinary chondrites using high‐resolution X‐ray computed tomography. The models show that metal‐troilite melting causes thermal buffering and inhibits the onset of silicate melting. Compared with models that ignore the effect of melting, our models predict longer cooling histories for the asteroids and accretion times that are earlier by 61, 124, or 113 kyr for the H, L, and LL asteroids, respectively. Because the Ni/Fe ratio of the metal and the bulk troilite/metal ratio is higher in L and LL chondrites than H chondrites, thermal buffering has the greatest effect in models for the L and LL chondrite parent bodies, and least effect for the H chondrite parent. Metal‐troilite melting is also relevant to models of primitive achondrite parent bodies, particularly those that underwent only low degrees of silicate partial melting. Thermal models can predict proportions of petrologic types formed within an asteroid, but are systematically different from the statistics of meteorite collections. A sampling bias is interpreted to explain these differences.     

Spade: An H chondrite impact‐melt breccia that experienced post‐shock annealing

Abstract— The low modal abundances of relict chondrules (1.8 vol%) and of coarse (i.e., ≥200 μm‐size) isolated mafic silicate grains (1.8 vol%) in Spade relative to mean H6 chondrites (11.4 and 9.8 vol%, respectively) show Spade to be a rock that has experienced a significant degree of melting. Various petrographic features (e.g., chromite‐plagioclase assemblages, chromite veinlets, silicate darkening) indicate that melting was caused by shock. Plagioclase was melted during the shock event and flowed so that it partially to completely surrounded nearby mafic silicate grains. During crystallization, plagioclase developed igneous zoning. Low‐Ca pyroxene that crystallized from the melt (or equilibrated with the melt at high temperatures) acquired relatively high amounts of CaO. Metallic Fe‐Ni cooled rapidly below the Fe‐Ni solvus and transformed into martensite. Subsequent reheating of the rock caused transformation of martensite into abundant duplex plessite. Ambiguities exist in the shock stage assignment of Spade. The extensive silicate darkening, the occurrence of chromite‐plagioclase assemblages, and the impact‐melted characteristics of Spade are consistent with shock stage S6. Low shock (stage S2) is indicated by the undulose extinction and lack of planar fractures in olivine. This suggests that Spade reached a maximum prior shock level equivalent to stage S6 and then experienced post‐shock annealing (probably to stage S1). These events were followed by a less intense impact that produced the undulose extinction in the olivine, characteristic of shock stage S2. Annealing could have occurred if Spade were emplaced near impact melts beneath the crater floor or deposited in close proximity to hot debris within an ejecta blanket. Spade firmly establishes the case for post‐shock annealing. This may have been a common process on OC asteroids.     

The formation and alteration of the Renazzo‐like carbonaceous chondrites III: Toward understanding the genesis of ferromagnesian chondrules

To better understand the formation conditions of ferromagnesian chondrules from the Renazzo‐like carbonaceous (CR) chondrites, a systematic study of 210 chondrules from 15 CR chondrites was conducted. The texture and composition of silicate and opaque minerals from each observed FeO‐rich (type II) chondrule, and a representative number of FeO‐poor (type I) chondrules, were studied to build a substantial and self‐consistent data set. The average abundances and standard deviations of Cr₂O₃ in FeO‐rich olivine phenocrysts are consistent with previous work that the CR chondrites are among the least thermally altered samples from the early solar system. Type II chondrules from the CR chondrites formed under highly variable conditions (e.g., precursor composition, redox conditions, cooling rate), with each chondrule recording a distinct igneous history. The opaque minerals within type II chondrules are consistent with formation during chondrule melting and cooling, starting as S‐ and Ni‐rich liquids at 988–1350 °C, then cooling to form monosulfide solid solution (mss) that crystallized around olivine/pyroxene phenocrysts. During cooling, Fe,Ni‐metal crystallized from the S‐ and Ni‐rich liquid, and upon further cooling mss decomposed into pentlandite and pyrrhotite, with pentlandite exsolving from mss at 400–600 °C. The composition, texture, and inferred formation temperature of pentlandite within chondrules studied here is inconsistent with formation via aqueous alteration. However, some opaque minerals (Fe,Ni‐metal versus magnetite and panethite) present in type II chondrules are a proxy for the degree of whole‐rock aqueous alteration. The texture and composition of sulfide‐bearing opaque minerals in Graves Nunataks 06100 and Grosvenor Mountains 03116 suggest that they are the most thermally altered CR chondrites.     

Opal‐A in the Nakhla meteorite: A tracer of ephemeral liquid water in the Amazonian crust of Mars

The nakhlite meteorites are clinopyroxenites that are derived from a ~1300 million year old sill or lava flow on Mars. Most members of the group contain veins of iddingsite whose main component is a fine‐grained and hydrous Fe‐ and Mg‐rich silicate. Siderite is present in the majority of veins, where it straddles or cross‐cuts the Fe‐Mg silicate. This carbonate also contains patches of ferric (oxy)hydroxide. Despite 40 years of investigation, the mineralogy and origins of the Fe‐Mg silicate is poorly understood, as is the paragenesis of the iddingsite veins. Nanometer‐scale analysis of Fe‐Mg silicate in the Nakhla meteorite by electron and X‐ray imaging and spectroscopy reveals that its principal constituents are nanoparticles of opal‐A. This hydrous and amorphous phase precipitated from acidic solutions that had become supersaturated with respect to silica by dissolution of olivine. Each opal‐A nanoparticle is enclosed within a ferrihydrite shell that formed by oxidation of iron that had also been liberated from the olivine. Siderite crystallized subsequently and from solutions that were alkaline and reducing, and replaced both the nanoparticles and olivine. The fluids that formed both the opal‐A/ferrihydrite and the siderite were sourced from one or more reservoirs in contact with the Martian atmosphere. The last event recorded by the veins was alteration of the carbonate to a ferric (oxy)hydroxide that probably took place on Mars, although a terrestrial origin remains possible. These results support findings from orbiter‐ and rover‐based spectroscopy that opaline silica was a common product of aqueous alteration of the Martian crust.     

Eutectic metal + troilite + Fe‐Mn‐Na phosphate + Al‐free chromite assemblage in shock‐produced chondritic melt of the Yanzhuang chondrite

An assemblage with FeNi metal, troilite, Fe‐Mn‐Na phosphate, and Al‐free chromite was identified in the metal‐troilite eutectic nodules in the shock‐produced chondritic melt of the Yanzhuang H6 meteorite. Electron microprobe and Raman spectroscopic analyses show that a few phosphate globules have the composition of Na‐bearing graftonite (Fe_,Mn,Na)₃(PO₄)₂, whereas most others correspond to Mn‐bearing galileiite Na(Fe,Mn)₄(PO₄)₃ and a possible new phosphate phase of Na₂(Fe,Mn)₁₇(PO₄)₁₂ composition. The Yanzhuang meteorite was shocked to a peak pressure of 50 GPa and a peak temperature of approximately 2000 °C. All minerals were melted after pressure release to form a chondritic melt due to very high postshock heat that brought the chondrite material above its liquidus. The volatile elements P and Na released from whitlockite and plagioclase along with elements Cr and Mn released from chromite are concentrated into the shock‐produced Fe‐Ni‐S‐O melt at high temperatures. During cooling, microcrystalline olivine and pyroxene first crystallized from the chondritic melt, metal‐troilite eutectic intergrowths, and silicate melt glass finally solidified at about 950–1000 °C. On the other hand, P, Mn, and Na in the Fe‐Ni‐S‐O melt combined with Fe and crystallized as Fe‐Mn‐Na phosphates within troilite, while Cr combined with Fe and crystallized as Al‐free chromite also within troilite.     

The silicate inclusions of the Ocotillo IAB iron meteorite

Abstract— The Ocotillo IAB iron meteorite contains small silicate inclusions consisting of olivine, low-Ca pyroxene, chromian diopside, plagioclase, magnesiochromite, apatite, troilite and metal. The ferromagnesian silicates have a small range of Fe/(Fe + Mg) ratios that are not due to zoning. These phases appear to be not well equilibrated. The FeO content of magnesiochromite is lower than values normally seen in silicate assemblages in IAB iron meteorites. The minerals in Ocotillo are generally like silicate assemblages in other IAB meteorites, covering similar composition ranges and exhibiting a metamorphic (granoblastic) texture. An estimate was made of the bulk composition of Ocotillo silicate inclusions. The bulk composition is close to that of ordinary chondrites with the exception of a deficiency in CaO that might be due to a sampling problem associated with the method used to estimate the bulk composition.     

Complex origins of silicate veinlets in HED meteorites: A case study of Northwest Africa 1109

We report on the petrography and mineralogy of three types of silicate veinlets in the brecciated eucrite Northwest Africa (NWA) 1109. These include Fe‐rich olivine, Mg‐rich olivine, and pyroxene veinlets. The Fe‐rich olivine veinlets mainly infill fractures in pyroxene and also occur along grain boundaries between pyroxene and plagioclase crystals, in both nonequilibrated and equilibrated lithic clasts. The host pyroxene of Fe‐rich olivine veinlets shows large chemical variations between and within grains. The Fe‐rich olivine veinlets also contain fine‐grained Fe³⁺‐bearing chromite, highly calcic plagioclase, merrillite, apatite, and troilite. Based on texture and mineral chemistry, we argue that the formation of Fe‐rich olivine was related to fluid deposition at relatively high temperatures. However, the source of Fe‐rich olivine in the veinlets remains unclear. Magnesium‐rich olivine veinlets were found in three diogenitic lithic clasts. In one of these, the Mg‐rich olivine veinlets only occur in one of the fine‐grained interstitial regions and extend into fractures within surrounding coarse‐grained orthopyroxene. Based on the texture of the interstitial materials, we suggest that the Mg‐rich olivine veinlets formed by shock‐induced localized melting and recrystallization. Pyroxene veinlets were only observed in one clast where they infill fractures within large plagioclase grains and are associated with fine‐grained pyroxene surrounding coarse‐grained pyroxene. The large chemical variations in pyroxene and the fracture‐filling texture indicate that the pyroxene veinlets might also have formed by shock‐induced localized melting and rapid crystallization. Our study demonstrates that silicate veinlets formed by a range of different surface processes on the surface of Vesta.     

Thuathe,a new H4/5 chondrite from Lesotho: History of the fall,petrography, and geochemistry

Abstract— On July 21, 2002, a meteorite fall occurred over the Thuathe plateau of western Lesotho. The well‐defined strewn field covers an area of 1.9 times 7.4 km. Many of the recovered specimens display a brecciated texture with leucocratic, angular to subrounded clasts in a somewhat darker groundmass. Mineralogical and chemical data, as well as oxygen isotopic analysis, indicate that Thuathe is an H4/5, S2/3 meteorite, with local H3 or H6 character. A number of anomalous features include somewhat high Co contents of kamacite and taenite relative to normal H‐group chondrites. Oxygen isotopic data plot at the edge of the normal H chondrite data field. Variable contents of metallic mineral phases and troilite result in a heterogeneous bulk composition (e.g., with regard to Si, Fe, and Mg), resulting in a spread of major element ratios that is not consistent with previously accepted H‐group composition. Trace element abundances are generally consistent with H chondritic composition, and Kr and Xe isotopic data agree with an H4 classification for this meteorite. Noble gas analysis gave U, Th‐⁴He gas retention and K‐Ar ages typical for H chondrites; no major thermal event affected this material since ～3.7 Ga. The exposure age for Thuathe is 5 Ma, somewhat lower than for other H chondrites. Cosmogenic nuclide analysis indicates a pre‐atmospheric radius of this meteorite between 35 and 40 cm. In the absence of evidence for solar gases, we classify Thuathe as a fragmental breccia. Numerous narrow, black veins cut across samples of Thuathe and are the result of a brittle deformation event that also caused local melting, especially in portions rich in sulfide. The formation of these veinlets is not the result of locally enhanced shock pressures (i.e., of shock melting) but rather of shearing under brittle conditions with local, friction‐related temperature excursions causing melting mostly of Fe‐sulfide and FeNi‐metal but also, locally, of silicate minerals. Frictional temperature excursions must have attained values in excess of 1500 °C to permit complete melting of forsteritic olivine.