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.     

Petrology and geochemistry of a silicate clast from the Mount Padbury mesosiderite: Implications for metal‐silicate mixing events of mesosiderite

Abstract— Petrological and bulk geochemical studies were performed on a large silicate clast from the Mount Padbury mesosiderite. The silicate clast is composed mainly of pyroxene and plagioclase with minor amounts of ilmenite, spinel, and other accessory minerals, and it shows subophitic texture. Pyroxenes in the clast are similar to those in type 5 eucrites and could have experienced prolonged thermal metamorphism after rapid crystallization from a near‐surface melt. Ilmenite and spinel vary chemically, indicating growth under disequilibrium conditions. The clast seems to have experienced an episode of rapid reheating and cooling, possibly as a result of metal‐silicate mixing. Abundances of siderophile elements are obviously higher than in eucrites, although the clast is also extremely depleted in highly siderophile elements. The fractionated pattern can be explained by injection of Fe‐FeS melts generated by partial melting of metallic portions during metal‐silicate mixing. The silicate clast had a complex petrogenesis that could have included: 1) rapid crystallization from magma in a lava flow or a shallow intrusion; 2) prolonged thermal metamorphism to equilibrate the mineral compositions of pyroxene and plagioclase after primary crystallization; 3) metal‐silicate mixing probably caused by the impact of solid metal bodies on the surface of the mesosiderite parent body; and 4) partial melting of metal and sulfide portions (and silicate in some cases) caused by the collisional heating, which produced Fe‐FeS melts with highly fractionated siderophile elements that were injected into silicate portions along cracks and fractures.     

Shock‐induced formation of wüstite and fayalite in a magnetite‐quartz target rock

Projectile–target interactions as a result of a large bolide impact are important issues, as abundant extraterrestrial material has been delivered to the Earth throughout its history. Here, we report results of shock‐recovery experiments with a magnetite‐quartz target rock positioned in an ARMCO iron container. Petrography, synchrotron‐assisted X‐ray powder diffraction, and micro‐chemical analysis confirm the appearance of wüstite, fayalite, and iron in targets subjected to 30 GPa. The newly formed mineral phases occur along shock veins and melt pockets within the magnetite‐quartz aggregates, as well as along intergranular fractures. We suggest that iron melt formed locally at the contact between ARMCO container and target, and intruded the sample causing melt corrosion at the rims of intensely fractured magnetite and quartz. The strongly reducing iron melt, in the form of μm‐sized droplets, caused mainly a diffusion rim of wüstite with minor melt corrosion around magnetite. In contact with quartz, iron reacted to form an iron‐enriched silicate melt, from which fayalite crystallized rapidly as dendritic grains. The temperatures required for these transformations are estimated between 1200 and 1600 °C, indicating extreme local temperature spikes during the 30 GPa shock pressure experiments.     

Origin of kamacite,schreibersite, and perryite in metal‐sulfide nodules of the enstatite chondrite Sahara 97072 (EH3)

Abstract– Perryite [(Fe,Ni)_x(Si,P)_y], schreibersite [(Fe,Ni)₃P], and kamacite (αFeNi) are constituent minerals of the metal‐sulfide nodules in the Sahara 97072 (EH3) enstatite chondrite meteorite. We have measured concentrations of Ni, Cu, Ga, Au, Ir, Ru, and Pd in these minerals with laser ablation, inductively coupled plasma mass spectrometry (ICP‐MS). We also measured their Fe, Ni, P, Si, and Co concentrations with electron microprobe. In kamacite, ratios of Ru/Ir, Pd/Ir, and Pd/Ru cluster around their respective CI values and all elements analyzed plot near the intersection of the equilibrium condensation trajectory versus Ni and the respective CI ratios. In schreibersite, the Pd/Ru ratio is near the CI value and perryite contains significant Cu, Ga, and Pd. We propose that schreibersite and perryite formed separately near the condensation temperatures of P and Si in a reduced gas and were incorporated into Fe‐Ni alloy. Upon further cooling, sulfidation of Fe in kamacite resulted in the formation of additional perryite at the sulfide interface. Still later, transient heating re‐melted this perryite near the Fe‐FeS eutectic temperature during partial melting of the metal‐sulfide nodules. The metal‐sulfide nodules are pre‐accretionary objects that retain CI ratios of most siderophile elements, although they have experienced transient heating events.     

P‐O‐rich sulfide phase in CM chondrites: Constraints on its origin on the CM parent body

CM chondrites are a group of primitive meteorites that have recorded the alteration history of the early solar system. We report the occurrence, chemistry, and oxygen isotopic compositions of P‐O‐rich sulfide phase in two CM chondrites (Grove Mountains [GRV] 021536 and Murchison). This P‐O‐rich sulfide is a polycrystalline aggregate of nanometer‐size grains. It occurs as isolated particles or aggregates in both CM chondrites. These grains, in the matrix and in type‐I chondrules from Murchison, were partially altered into tochilinite; however, grains enclosed by Ca‐carbonate are much less altered. This P‐O‐rich sulfide in Murchison is closely associated with magnetite, FeNi phosphide, brezinaite (Cr₃S₄), and eskolaite (Cr₂O₃). In addition to sulfur as the major component, this sulfide contains ~6.3 wt% O, ~5.4 wt% P, and minor amounts of hydrogen. Analyses of oxygen isotopes by SIMS resulted in an average δ¹⁸O value of ?22.5 ‰ and an average Δ¹⁷O value of 0.2 ± 9.2 ‰ (2σ). Limited variations in both chemical compositions and electron‐diffraction patterns imply that the P‐O‐rich sulfide may be a single phase rather than a polyphase mixture. Several features indicate that this P‐O‐rich sulfide phase formed at low temperature on the parent body, most likely through the alteration of FeNi metal (a) close association with other low‐temperature alteration products, (b) the presence of hydrogen, (c) high Δ¹⁷O values and the presence in altered mesostasis of type‐I chondrules and absence in type‐II chondrules. The textural relations of the P‐O‐rich sulfide and other low‐temperature minerals reveal at least three episodic‐alteration events on the parent body of CM chondrites (1) formation of P‐O‐rich sulfide during sulfur‐rich aqueous alteration of P‐rich FeNi metal, (2) formation of Ca‐carbonate during local carbonation, and (3) alteration of P‐O‐rich sulfide and formation of tochilinite during a period of late‐stage intensive aqueous alteration.     

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.     

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.     

Si‐bearing metal and niningerite in Almahata Sitta fine‐grained ureilites and insights into the diversity of metal on the ureilite parent body

A detailed mineralogical and chemical study of Almahata Sitta fine‐grained ureilites (MS‐20, MS‐165, MS‐168) was performed to shed light on the origin of these lithologies and their sulfide and metal. The Almahata Sitta fine‐grained ureilites (silicates <30 μm grain size) show textural and chemical evidence for severe impact smelting as described for other fine‐grained ureilites. Highly reduced areas in Almahata Sitta fine‐grained ureilites show large (up to ～1 mm) Si‐bearing metal grains (up to ～4.5 wt% Si) and niningerite [Mg_>0.5,(Mn,Fe)_<0.5S] with some similarities to the mineralogy of enstatite (E) chondrites. Overall, metal grains show a large compositional variability in Ni and Si concentrations. Niningerite grains probably formed as a by‐product of smelting via sulfidation. The large Si‐Ni variation in fine‐grained ureilite metal could be the result of variable degrees of reduction during impact smelting, inherited from coarse‐grained ureilite precursors, or a combination of both. Large Si‐bearing metal grains probably formed via coalescence of existing and newly formed metal during impact smelting. Bulk and in situ siderophile trace element abundances indicate three distinct populations of (1) metal crystallized from partial melts in MS‐20, (2) metal resembling bulk chondritic compositions in MS‐165, and (3) residual metal in MS‐168. Almahata Sitta fine‐grained ureilites developed their distinctive mineralogy due to severe reduction during smelting. Despite the presence of E chondrite and ureilite stones in the Almahata Sitta fall, a mixing relation of E chondrites or their constituents and ureilite material in Almahata Sitta can be ruled out based on isotopic, textural, and mineral‐chemical reasons.     

A large shock vein in L chondrite Roosevelt County 106: Evidence for a long‐duration shock pulse on the L chondrite parent body

A large shock‐induced melt vein in L6 ordinary chondrite Roosevelt County 106 contains abundant high‐pressure minerals, including olivine, enstatite, and plagioclase fragments that have been transformed to polycrystalline ringwoodite, majorite, lingunite, and jadeite. The host chondrite at the melt‐vein margins contains olivines that are partially transformed to ringwoodite. The quenched silicate melt in the shock veins consists of majoritic garnets, up to 25 μm in size, magnetite, maghemite, and phyllosilicates. The magnetite, maghemite, and phyllosilicates are the terrestrial alteration products of magnesiowüstite and quenched glass. This assemblage indicates crystallization of the silicate melt at approximately 20–25 GPa and 2000 °C. Coarse majorite garnets in the centers of shock veins grade into increasingly finer grained dendritic garnets toward the vein margins, indicating increasing quench rates toward the margins as a result of thermal conduction to the surrounding chondrite host. Nanocrystalline boundary zones, that contain wadsleyite, ringwoodite, majorite, and magnesiowüstite, occur along shock‐vein margins. These zones represent rapid quench of a boundary melt that contains less metal‐sulfide than the bulk shock vein. One‐dimensional finite element heat‐flow calculations were performed to estimate a quench time of 750–1900 ms for a 1.6‐mm thick shock vein. Because the vein crystallized as a single high‐pressure assemblage, the shock pulse duration was at least as long as the quench time and therefore the sample remained at 20–25 GPa for at least 750 ms. This relatively long shock pulse, combined with a modest shock pressure, implies that this sample came from deep in the L chondrite parent body during a collision with a large impacting body, such as the impact event that disrupted the L chondrite parent body 470 Myr ago.     

Silica‐rich igneous rims around magnesian chondrules in CR carbonaceous chondrites: Evidence for condensation origin from fractionated nebular gas

Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO₂ phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr₂O₃) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na₂O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO_(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.     

QUE 94204: A primitive enstatite achondrite produced by the partial melting of an E chondrite‐like protolith

Abstract– Queen Alexandra Range (QUE) 94204, an enstatite achondrite, is a coarse‐grained, highly recrystallized, chondrule‐free and unbrecciated rock dominated (about 70 vol%) by anhedral, equigranular crystals of orthoenstatite of nearly endmember composition (Fs_0.1–0.4, Wo_0.3–0.4) with interstitial plagioclase, kamacite, and troilite. Abundance of approximately 120° triple junctions and the close association of metal–sulfide and plagioclase‐rich melts indicate that QUE 94204 has undergone limited partial melting with inefficient melt extraction. Mineral chemistry indicates a high degree of thermal metamorphism. Kamacite in QUE 94204 contains between 2.09 and 2.55 wt% Si, similar to highly metamorphosed EL chondrites. Plagioclase has between 4.31 and 6.66 wt% CaO, higher than other E chondrites but closer in composition to plagioclase from metamorphosed EL chondrites. QUE 94204 troilite contains up to 2.55 wt% Ti, consistent with extensive thermal metamorphism of an E chondrite‐like precursor. Results presented in this study indicate that QUE 94204 is the result of low degree, (about 5–20 vol%, probably toward the lower end of this range) partial melting of an E chondrite protolith. Textural and chemical evidence suggests that during the metamorphism of QUE 94204, melts formed first at the Fe,Ni‐FeS cotectic near approximately 900 °C, followed by plagioclase‐pyroxene silicate partial melts near approximately 1100 °C. Neither the Fe,Ni‐FeS nor the plagioclase‐pyroxene melts were efficiently segregated or extracted. QUE 94204 belongs to a grouplet of similar “primitive enstatite achondrites” that are analogous to the acapulcoites‐lodranites, but that have resulted from the partial melting of an E chondrite‐like protolith.     

Differentiation processes in FeO‐rich asteroids revealed by the achondrite Lewis Cliff 88763

Olivine‐dominated (70–80 modal %) achondrite meteorite Lewis Cliff (LEW) 88763 originated from metamorphism and limited partial melting of a FeO‐rich parent body. The meteorite experienced some alteration on Earth, evident from subchondritic Re/Os, and redistribution of rhenium within the sample. LEW 88763 is texturally similar to winonaites, has a Δ¹⁷O value of ?1.19 ± 0.10‰, and low bulk‐rock Mg/(Mg+Fe) (0.39), similar to the FeO‐rich cumulate achondrite Northwest Africa (NWA) 6693. The similar bulk‐rock major‐, minor‐, and trace‐element abundances of LEW 88763, relative to some carbonaceous chondrites, including ratios of Pd/Os, Pt/Os, Ir/Os, and ¹⁸⁷Os/¹⁸⁸Os (0.1262), implies a FeO‐ and volatile‐rich precursor composition. Lack of fractionation of the rare earth elements, but a factor of approximately two lower highly siderophile element abundances in LEW 88763, compared with chondrites, implies limited loss of Fe‐Ni‐S melts during metamorphism and anatexis. These results support the generation of high Fe/Mg, sulfide, and/or metal‐rich partial melts from FeO‐rich parent bodies during partial melting. In detail, however, LEW 88763 cannot be a parent composition to any other meteorite sample, due to highly limited silicate melt loss (0 to <<5%). As such, LEW 88763 represents the least‐modified FeO‐rich achondrite source composition recognized to date and is distinct from all other meteorites. LEW 88763 should be reclassified as an anomalous achondrite that experienced limited Fe,Ni‐FeS melt loss. Lewis Cliff 88763, combined with a growing collection of FeO‐rich meteorites, such as brachinites, brachinite‐like achondrites, the Graves Nunataks (GRA) 06128/9 meteorites, NWA 6693, and Tafassasset, has important implications for understanding the initiation of planetary differentiation. Specifically, regardless of precursor compositions, partial melting and differentiation processes appear to be similar on asteroidal bodies spanning a range of initial oxidation states and volatile contents.     

Fe‐Ni metal in primitive chondrites: Indicators of classification and metamorphic conditions for ordinary and CO chondrites

Abstract— We report the results of our petrological and mineralogical study of Fe‐Ni metal in type 3 ordinary and CO chondrites, and the ungrouped carbonaceous chondrite Acfer 094. Fe‐Ni metal in ordinary and CO chondrites occurs in chondrule interiors, on chondrule surfaces, and as isolated grains in the matrix. Isolated Ni‐rich metal in chondrites of petrologic type lower than type 3.10 is enriched in Co relative to the kamacite in chondrules. However, Ni‐rich metal in type 3.15–3.9 chondrites always contains less Co than does kamacite. Fe‐Ni metal grains in chondrules in Semarkona typically show plessitic intergrowths consisting of submicrometer kamacite and Ni‐rich regions. Metal in other type 3 chondrites is composed of fine‐ to coarse‐grained aggregates of kamacite and Ni‐rich metal, resulting from metamorphism in the parent body. We found that the number density of Ni‐rich grains in metal (number of Ni‐rich grains per unit area of metal) in chondrules systematically decreases with increasing petrologic type. Thus, Fe‐Ni metal is a highly sensitive recorder of metamorphism in ordinary and carbonaceous chondrites, and can be used to distinguish petrologic type and identify the least thermally metamorphosed chondrites. Among the known ordinary and CO chondrites, Semarkona is the most primitive. The range of metamorphic temperatures were similar for type 3 ordinary and CO chondrites, despite them having different parent bodies. Most Fe‐Ni metal in Acfer 094 is martensite, and it preserves primary features. The degree of metamorphism is lower in Acfer 094, a true type 3.00 chondrite, than in Semarkona, which should be reclassified as type 3.01.     

The Fountain Hills impact‐modified CB chondrite and thermal history of the CB asteroid

Abstract— Fountain Hills is a metal‐rich chondrite with mineral and whole chondrite oxygen isotope compositions that suggest it is a CB chondrite. However, its petrologic characteristics suggest that it has been modified by shock and recrystallization to a greater degree than other CB chondrites. It differs texturally from the CB chondrites in that its metal is interstitial to the silicate and does not occur as discrete clasts as in the other CB chondrites. Portions of Fountain Hills appear to be recrystallized and it contains large (mm‐size) olivine rimmed by pyroxene. A characteristic of the CB chondrites is the presence of small sulfide blebs in large metal clasts and anomalously heavy (¹⁵N‐enriched) nitrogen often associated with metal surrounding the sulfide blebs, but Fountain Hills lacks sulfide and its nitrogen is relatively light. The differences between Fountain Hills and the other CB chondrites can be attributed to a secondary process, most likely impact‐melting and recrystallization, that overprinted its primary features and it is inferred that Fountain Hills is an impact‐modified CB chondrite.     

Two distinct assemblages of high‐pressure liquidus phases in shock veins of the Sixiangkou meteorite

Abstract— Shock‐produced complex veins, including earlier and later veins, are identified in the Sixiangkou L6 chondrite. The early vein is intersected by the late vein and consists of coarse‐grained aggregates of ringwoodite, majorite, and lingunite, and fragments of olivine, pyroxene, plagioclase, metal, and troilite, as well as a fine‐grained matrix of garnet, ringwoodite, metal, and troilite. The late vein mainly consists of a fine‐grained matrix of garnet, magnesiowüstite, metal, and troilite, as well as a small amount of coarse‐grained aggregates. The amount of fine‐grained matrix suggests that the late vein was nearly completely melted, whereas the early vein underwent partial melting. Both fine‐grained assemblages of garnet plus ringwoodite in the early vein and garnet plus magnesiowüstite in the late vein are liquidus phases crystallized from shock‐induced melt. Based on our understanding of the liquidus assemblages, the late vein experienced a higher pressure and temperature than the early vein.     

Along‐track compositional and textural variation in extensively melted grains returned from comet 81P/Wild 2 by the Stardust mission: Implications for capture‐melting process

Abstract— Five amorphous (extensively melted) grains from Stardust aerogel capture Track 35 were examined by transmission electron microscopy (TEM); two from the bulb, two from near the bulb‐stylus transition, and one from near the terminal particle. Melted grains consist largely of a texturally and compositionally heterogeneous emulsion of immiscible metal/sulfide beads nanometers to tens of nanometers in diameter in a silica‐rich vesicular glass. Most metal/sulfide beads are spherical, but textures of non‐spherical beads indicate that some solidified as large drops during stretching and breaking while in translational and rotational motion, and others solidified from lenses of immiscible liquid at the silicate‐melt/vesicle (vapor) interface. Melted grains appear to become richer in Fe relative to Mg, and depleted in S relative to Fe and Ni with increasing penetration distance along the aerogel capture track. Fe/S ratios are near unity in grains from the bulb of Track 35, consistent with the dominance of Fe‐monosulfide minerals inferred by previous research on Stardust materials. Near‐stoichiometric Fe/S in melted grains from the bulb suggests that Fe‐sulfides in the bulb were dispersed and melted during formation of the bulb but did not lose S. Along‐track increases in Fe/S in melted grains from the bulb through the bulb‐stylus transition and continuing into the stylus indicate that S initially present as iron monosulfide may have been progressively partially volatilized and lost from the melted grains with greater penetration of the grains deeper into the aerogel during capture‐melting of comet dust. Extensively melted grains from the bulbs of aerogel capture tracks may preserve better primary compositional information with less capture‐related modification than grains from farther along the same capture tracks.     

Petrogenesis and shock metamorphism of the enriched lherzolitic shergottite Northwest Africa 7755

Northwest Africa (NWA) 7755 is a newly found enriched lherzolitic shergottite. Here, we report its detailed petrography and mineralogy. NWA 7755 contains both poikilitic and non‐poikilitic lithologies. Olivine has different compositional ranges in the poikilitic and non‐poikilitic lithologies, Fa_30–39 and Fa_37–40, respectively. Pyroxene in the non‐poikilitic lithology is systematically Fe‐richer than that in the poikilitic lithology. The chromite grains in non‐poikilitic lithology are highly Ti‐richer than those in the poikilitic lithology. The chemical variations of olivine, pyroxene, and chromite between the poikilitic and non‐poikilitic lithologies support a two‐stage formation model of lherzolitic shergottites. Besides planar fractures and strong mosaicism in olivine and pyroxene, shock‐induced melt veins and pockets are observed in NWA 7755. Olivine grains within and adjacent to melt veins and/or pockets have either transformed to ringwoodite, amorphous phase, or dissociated to bridgmanite plus magnesiowüstite. Merrillite in melt veins has completely transformed to tuite; however, apatite only has partially transformed to tuite, indicating a relatively sluggish transformation rate. The partial transformation from apatite to tuite resulted in fractional devolatilization of Cl and F in apatite. The fine‐grained mineral assemblage in melt veins consists mainly of bridgmanite, minor magnesiowüstite, Fe‐sulfide, Fe‐phosphide, and Ca‐phosphate minerals. The coexistence of bridgmanite and magnesiowüstite in these veins indicates a shock pressure of >~24 GPa and a temperature of 1800–2000 °C. Coesite and seifertite are probably present in NWA 7755. The presence of these high‐pressure minerals indicates that NWA 7755 has experienced a more intense shock metamorphism than other enriched lherzolitic shergottites.     

New observations on high‐pressure phases in a shock melt vein in the Villalbeto de la Peña meteorite: Insights into the shock behavior of diopside

The petrology and mineralogy of shock melt veins in the L6 ordinary chondrite host of Villalbeto de la Peña, a highly shocked, L chondrite polymict breccia, have been investigated in detail using scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, and electron probe microanalysis. Entrained olivine, enstatite, diopside, and plagioclase are transformed into ringwoodite, low‐Ca majorite, high‐Ca majorite, and an assemblage of jadeite‐lingunite, respectively, in several shock melt veins and pockets. We have focused on the shock behavior of diopside in a particularly large shock melt vein (10 mm long and up to 4 mm wide) in order to provide additional insights into its high‐pressure polymorphic phase transformation mechanisms. We report the first evidence of diopside undergoing shock‐induced melting, and the occurrence of natural Ca‐majorite formed by solid‐state transformation from diopside. Magnesiowüstite has also been found as veins injected into diopside in the form of nanocrystalline grains that crystallized from a melt and also occurs interstitially between majorite‐pyrope grains in the melt‐vein matrix. In addition, we have observed compositional zoning in majorite‐pyrope grains in the matrix of the shock‐melt vein, which has not been described previously in any shocked meteorite. Collectively, all these different lines of evidence are suggestive of a major shock event with high cooling rates. The minimum peak shock conditions are difficult to constrain, because of the uncertainties in applying experimentally determined high‐pressure phase equilibria to complex natural systems. However, our results suggest that conditions between 16 and 28 GPa and 2000–2200 °C were reached.     

Opaque assemblages in CR2 Graves Nunataks (GRA) 06100 as indicators of shock‐driven hydrothermal alteration in the CR chondrite parent body

We have studied the petrologic characteristics of sulfide‐metal lodes, polymineralic Fe‐Ni nodules, and opaque assemblages in the CR2 chondrite Graves Nunataks (GRA) 06100, one of the most altered CR chondrites. Unlike low petrologic type CR chondrites, alteration of metal appears to have played a central role in the formation of secondary minerals in GRA 06100. Differences in the mineralogy and chemical compositions of materials in GRA 06100 suggest that it experienced higher temperatures than other CR2 chondrites. Mineralogic features indicative of high temperature include: (1) exsolution of Ni‐poor and Ni‐rich metal from nebular kamacite; (2) formation of sulfides, oxides, and phosphates; (3) changes in the Co/Ni ratios; and (4) carbidization of Fe‐Ni metal. The conspicuous absence of pentlandite may indicate that peak temperatures exceeded 600 °C. Opaques appear to have been affected by the action of aqueous fluids that resulted in the formation of abundant oxides, Fe‐rich carbonates, including endmember ankerite, and the sulfide‐silicate‐phosphate scorzalite. We suggest that these materials formed via impact‐driven metamorphism. Mineralogic features indicative of impact metamorphism include (1) the presence of sulfide‐metal lodes; (2) the abundance of polymineralic opaque assemblages with mosaic‐like textures; and (3) the presence of suessite. Initial shock metamorphism probably resulted in replacement of nebular Fe‐Ni metal in chondrules and in matrix by Ni‐rich, Co‐rich Fe metal, Al‐Ti‐Cr‐rich alloys, and Fe sulfides, while subsequent hydrothermal alteration produced accessory oxides, phosphates, and Fe carbonates. An extensive network of sulfide‐metal veins permitted effective exchange of siderophile elements from pre‐existing metal nodules with adjacent chondrules and matrix, resulting in unusually high Fe contents in these objects.