Genesis of the IIICD iron meteorites: Evidence from silicate-bearing inclusions

Abstract— Our studies of the silicate-bearing inclusions in the IIICD iron meteorites Maltahöhe, Carlton and Dayton suggest that their mineralogy and mineral compositions are related to the composition of the metal in the host meteorites. An inclusion in the low-Ni Maltahöhe is similar in mineralogy to those in IAB irons, which contain olivine, pyroxene, plagioclase, graphite and troilite. With increasing Ni concentration of the metal, silicate inclusions become poorer in graphite, richer in phosphates, and the phosphate and silicate assemblages become more complex. Dayton contains pyroxene, plagioclase, SiO₂, brianite, panethite and whitlockite, without graphite. In addition, mafic silicates become more FeO-rich with increasing Ni concentration of the hosts. In contrast, silicates in IAB irons show no such correlation with host Ni concentration, nor do they have the complex mineral assemblages of Dayton. These trends in inclusion composition and mineralogy in IIICD iron meteorites have been established by reactions between the S-rich metallic magma and the silicates, but the physical setting is uncertain. Of the two processes invoked by other authors to account for groups IAB and IIICD, fractional crystallization of S-rich cores and impact generation of melt pools, we prefer core crystallization. However, the absence of relationships between silicate inclusion mineralogy and metal compositions among IAB irons analogous to those that we have discovered in IIICD irons suggests that the IAB and IIICD cores/metallic magmas evolved in rather different ways. We suggest that the solidification of the IIICD core may have been very complex, involving fractional crystallization, nucleation effects and, possibly, liquid immiscibility.     

The extremely reduced silicate‐bearing iron meteorite Northwest Africa 6583: Implications on the variety of the impact melt rocks of the IAB‐complex parent body

Northwest Africa (NWA) 6583 is a silicate‐bearing iron meteorite with Ni = 18 wt%. The oxygen isotope composition of the silicates (?′¹⁷O = ?0.439 ‰) indicates a genetic link with the IAB‐complex. Other chemical, mineralogical, and textural features of NWA 6583 are consistent with classification as a new member of the IAB‐complex. However, some unique features, e.g., the low Au content (1.13 μg g^?1) and the extremely reducing conditions of formation (approximately ?3.5 ?IW), distinguish NWA 6583 from the known IAB‐complex irons and extend the properties of this group of meteorites. The chemical and textural features of NWA 6583 can be ascribed to a genesis by impact melting on a parent body of chondritic composition. This model is also consistent with one of the most recent models for the genesis of the IAB‐complex. Northwest Africa 6583 provides a further example of the wide lithological and mineralogical variety that impact melting could produce on the surface of a single asteroid, especially if characterized by an important compositional heterogeneity in space and time like a regolith.     

Ar‐Ar and I‐Xe ages and the thermal history of IAB meteorites

Abstract— Studies of several samples of the large Caddo County IAB iron meteorite reveal andesitic material enriched in Si, Na, Al, and Ca, which is essentially unique among meteorites. This material is believed to have formed from a chondritic source by partial melting and to have further segregated by grain coarsening. Such an origin implies extended metamorphism of the IAB parent body. New ³⁹Ar‐⁴⁰Ar ages for silicate from three different Caddo samples are consistent with a common age of 4.50‐4.51 Gyr. Less well‐defined Ar‐Ar degassing ages for inclusions from two other IABs, EET (Elephant Moraine) 83333 and Udei Station, are ?4.32 Gyr, whereas the age for Campo del Cielo varies considerably over about 3.23‐4.56 Gyr. New ¹²⁹I‐¹²⁹Xe ages for Caddo County and EET 83333 are 4557.9 ± 0.1 Myr and 4557–4560 Myr, respectively, relative to an age of 4562.3 Myr for Shallowater. Considering all reported Ar‐Ar degassing ages for IABs and related winonaites, the range is ?4.32‐4.53 Gyr, but several IABs give similar Ar ages of 4.50‐4.52 Gyr. We interpret these older Ar ages to represent cooling after the time of last significant metamorphism on the parent body and the younger ages to represent later ⁴⁰Ar diffusion loss. The older Ar‐Ar ages for IABs are similar to Sm‐Nd and Rb‐Sr isochron ages reported in the literature for Caddo County. Considering the possibility that IAB parent body formation was followed by impact disruption, reassembly, and metamorphism (e.g., Benedix et al. 2000), the Ar‐Ar ages and IAB cooling rates deduced from Ni concentration profiles in IAB metal (Herpfer et al. 1994) are consistent if the time of the postassembly metamorphism was as late as about 4.53 Gyr ago. However, I‐Xe ages reported for some IABs define much older ages of about 4558–4566 Myr, which cannot easily be reconciled with the much younger Ar‐Ar and Sm‐Nd ages. An explanation for the difference in radiometric ages of IABs may reside in combinations of the following: a) I‐Xe ages have very high closure temperatures and were not reset during metamorphism about 4.53 Gyr ago; b) a bias exists in the ⁴⁰K decay constants which makes these Ar‐Ar ages approximately 30 Myr too young; c) the reported Sm‐Nd and Rb‐Sr ages for Caddo are in error by amounts equal to or exceeding their reported 2‐sigma uncertainties; and d) about 30 Myr after the initial heating that produced differentiation of Caddo silicate and mixing of silicate and metal, a mild metamorphism of the IAB parent body reset the Ar‐Ar ages.     

Siderophile element characteristics of acapulcoite–lodranites and winonaites: Implications for the early differentiation processes of their parent bodies

We have studied magnetic fractions of five acapulcoites, three lodranites, and two winonaites to investigate chemical compositions of their precursor materials and metallic partial melting processes occurring on their parent bodies. One winonaite metal is similar in composition to low Au, low Ni IAB iron subgroup, indicating genetic relationship between them. Magnetic fractions of chondrule‐bearing acapulcoite and winonaite have intermediate chemical compositions of metals between H chondrites and EL chondrites. This fact indicates that the precursor materials of acapulcoite–lodranites and winonaites were similar to H and/or EL chondrites in chemical compositions. Magnetic fractions in acapulcoite–lodranites have a large variety of chemical compositions. Most of them show enrichments of W, Re, Ir, Pt, Mo, and Rh, and one of them shows clear depletion in Re and Ir relative to those of chondrule‐bearing acapulcoite. Chemical compositional variations among acapulcoite–lodranite metals cannot be explained by a single Fe‐Ni‐S partial melting event, but a two‐step partial melting model can explain it.     

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.     

Sulfide‐rich metallic impact melts from chondritic parent bodies

Abstract– Sacramento Wash 005 (SaW) 005, Meteorite Hills 00428 (MET) 00428, and Mount Howe 88403 (HOW) 88403 are S‐rich Fe,Ni‐rich metal meteorites with fine metal structures and homogeneous troilite. We compare them with the H‐metal meteorite, Lewis Cliff 88432. Phase diagram analyses suggest that SaW 005, MET 00428, and HOW 88403 were liquids at temperatures above 1350 °C. Tridymite in HOW 88403 constrains formation to a high‐temperature and low‐pressure environment. The morphology of their metal‐troilite structures may suggest that MET 00428 cooled the slowest, SaW 005 cooled faster, and HOW 88403 cooled the quickest. SaW 005 and MET 00428 contain H‐chondrite like silicates, and SaW 005 contains a chondrule‐bearing inclusion that is texturally and compositionally similar to H4 chondrites. The compositional and morphological similarities of SaW 005 and MET 00428 suggest that they are likely the result of impact processing on the H‐chondrite parent body. SaW 005 and MET 00428 are the first recognized iron‐ and sulfide‐rich meteorites, which formed by impact on the H‐chondrite parent body, which are distinct from the IIE‐iron meteorite group. The morphological and chemical differences of HOW 88403 suggest that it is not from the H‐chondrite body, although it likely formed during an impact on a chondritic parent body.     

A TEM study of four particles extracted from the Stardust track 80

Abstract— Four particles extracted from track 80 at different penetration depths have been studied by analytical transmission electron microscopy (ATEM). Regardless of their positions within the track, the samples present a comparable microstructure made of a silica rich glassy matrix embedding a large number of small Fe‐Ni‐S inclusions and vesicles. This microstructure is typical of strongly thermally modified particles that were heated and melted during the hypervelocity impact into the aerogel. X‐ray intensity maps show that the particles were made of Mg‐rich silicates (typically 200 nm in diameter) cemented by a fine‐grained matrix enriched in iron sulfide. Bulk compositions of the four particles suggest that the captured dust particle was an aggregate of grains with various iron sulfide fraction and that no extending chemical mixing in the bulb occurred during the deceleration. The bulk S/Fe ratios of the four samples are close to CI and far from the chondritic meteorites from the asteroidal belt, suggesting that the studied particles are compatible with chondritic‐porous interplanetary dust particles or with material coming from a large heliocentric distance for escaping the S depletion.     

The Lueders,Texas, IAB iron meteorite with silicate inclusions

Abstract The Lueders iron meteorite with silicate inclusions was recovered as a single specimen of ～35.4 kg in Shackelford County, Texas, in 1973 and recognized as a meteorite in 1993. Siderophile element concentrations indicate chemical classification as a low-Ni IAB iron meteorite closely related to Landes; like Landes, it has a Cu content ～4σ above the main IAB-IIICD trend and therefore we also designate Lueders as an anomalous member of IAB. The metallic host is composed of equigranular kamacite but with a suggestion of octahedral structure and with a bandwidth of 1.4 mm, suggesting structural classification as a coarse octahedrite (Og). The meteorite contains ～23 wt% of roughly millimeter to centimeter-sized angular silicate inclusions. Classification as a IAB is confirmed by O isotopic analysis of silicate inclusions. These inclusions contain an assemblage rich in silicates, troilite and graphite; lack certain minor phases (e.g., daubreelite); and have angular shapes. A variety of processes (e.g., fragmentation, partial melting, reduction) appear to have played a significant role in the formation of Lueders and all IAB iron meteorites. Petrologic and chemical differences confirm that Lueders is not paired with the widely distributed Odessa meteorite.     

Interpreting the I‐Xe system in individual silicate grains from Toluca IAB

Abstract— Detailed isotopic and mineralogical studies of silicate inclusions separated from a troilite nodule of the Toluca IAB iron meteorite reveal the presence of radiogenic ¹²⁹Xe in chlorapatite, plagioclase, perryite, and pyroxene grains. Subsequent I‐Xe studies of 32 neutron‐irradiated pyroxene grains indicate that high‐Mg and low‐Mg pyroxenes have distinctive I‐Xe signatures. The I‐Xe system in high‐Mg pyroxenes closed at 4560.5 ± 2.4 Ma, probably reflecting exsolution of silicates from the melt, while the low‐Mg pyroxenes closed at 4552.0 ± 3.7 Ma, 8.5 Ma later, providing a means for determining the cooling rate at the time of exsolution. If the host Toluca graphite‐troilite‐rich inclusion formed after the breakup and reassembly of the IAB parent body as has been suggested, the I‐Xe ages of the high‐Mg pyroxenes separated from this inclusions indicate that this catastrophic impact occurred not later than 4560.5 Ma, 6.7 Ma after formation of CAIs. The cooling rate at the time of silicates exsolution in Toluca is 14.5 ± 10.0 °C/Ma.     

Differentiation and evolution of the IVA meteorite parent body: Clues from pyroxene geochemistry in the Steinbach stony‐iron meteorite

Abstract— We analyzed the Steinbach IVA stony‐iron meteorite using scanning electron microscopy (SEM), electron microprobe analysis (EMPA), laser ablation inductively‐coupled‐plasma mass spectroscopy (LA‐ICP‐MS), and modeling techniques. Different and sometimes adjacent low‐Ca pyroxene grains have distinct compositions and evidently crystallized at different stages in a chemically evolving system prior to the solidification of metal and troilite. Early crystallizing pyroxene shows evidence for disequilibrium and formation under conditions of rapid cooling, producing clinobronzite and type 1 pyroxene rich in troilite and other inclusions. Subsequently, type 2 pyroxene crystallized over an extensive fractionation interval. Steinbach probably formed as a cumulate produced by extensive crystal fractionation (?60–70% fractional crystallization) from a high‐temperature (?1450–1490 °C) silicate‐metallic magma. The inferred composition of the precursor magma is best modeled as having formed by ≥30–50% silicate partial melting of a chondritic protolith. If this protolith was similar to an LL chondrite (as implied by O‐isotopic data), then olivine must have separated from the partial melt, and a substantial amount (?53–56%) of FeO must have been reduced in the silicate magma. A model of simultaneous endogenic heating and collisional disruption appears best able to explain the data for Steinbach and other IVA meteorites. Impact disruption occurred while the parent body was substantially molten, causing liquids to separate from solids and oxygen‐bearing gas to vent to space, leading to a molten metal‐rich body that was smaller than the original parent body and that solidified from the outside in. This model can simultaneously explain the characteristics of both stony‐iron and iron IVA meteorites, including the apparent correlation between metal composition and metallographic cooling rate observed for metal.     

Carbon‐silicate aggregates in the CH chondrite Pecora Escarpment 91467: A carrier of heavy nitrogen of interstellar origin

Abstract— Scanning electron microscopy and secondary ion mass spectrometry of the unequilibrated CH chondrite Pecora Escarpment (PCA) 91467 revealed four carriers of isotopically heavy N: (1) aggregates of carbonaceous material and silicates, (2) iron‐nickel metal grains with fine Fe‐Cr sulfide inclusions, (3) Si‐rich Fe‐Ni metal associated with Fe‐sulfide and (4) hydrated areas in the matrix. N in carbon‐silicate aggregates is isotopically heavy (δ¹⁵N is as high as 2500%0), whereas the other elements are isotopically normal, suggesting interstellar origin of carbonaceous material in the aggregates. Based on isotopic and textural evidence, we suggest that the carriers (2) and (3) were formed by brief heating in the solar nebula, whereas the carrier (4) was formed in a parent‐body asteroid. The carbon‐silicate aggregates are likely to be related to interstellar graphite found in Murchison and may also be the source of heavy N in bencubbinites.     

The halite‐bearing Zag and Monahans (1998) meteorite breccias: Shock metamorphism,thermal metamorphism and aqueous alteration on the H‐chondrite parent body

Abstract— Zag and Monahans (1998) are H‐chondrite regolith breccias comprised mainly of light‐colored metamorphosed clasts, dark clasts that exhibit extensive silicate darkening, and a halite‐bearing clastic matrix. These meteorites reflect a complex set of modification processes that occurred on the H‐chondrite parent body. The light‐colored clasts are thermally metamorphosed H5 and H6 rocks that were fragmented and deposited in the regolith. The dark clasts formed from light‐colored clasts during shock events that melted and mobilized a significant fraction of their metallic Fe‐Ni and troilite grains. The clastic matrices of these meteorites are rich in solar‐wind gases. Parent‐body water was required to cause leaching of chondritic minerals and chondrule glass; the fluids became enriched in Na, K, Cl, Br, Al, Ca, Mg and Fe. Evaporation of the fluids caused them to become brines as halides and alkalies became supersaturated; grains of halite (and, in the case of Monahans (1998), halite with sylvite inclusions) precipitated at low temperatures (≤100 °C) in the porous regolith. In both meteorites fluid inclusions were trapped inside the halite crystals. Primary fluid inclusions were trapped in the growing crystals; secondary inclusions formed subsequently from fluid trapped within healed fractures.     

The effects of disk building on the distributions of refractory materials in the solar nebula

Abstract– Refractory materials, such as calcium‐aluminum‐rich inclusions (CAIs) and crystalline silicates, are widely found in chondritic meteorites as well as comets, taken as evidence for large‐scale mixing in the solar nebula. Most models for mixing in the solar nebula begin with a well‐formed protoplanetary disk. Here, we relax this assumption by modeling the formation and evolution of the solar nebula during and after the period when it accreted material from its parent molecular cloud. We consider how disk building impacts the long‐term evolution of the disk and the implications for grain transport and mixing within it. Our model shows that materials that formed before infall was complete could be preserved in primitive bodies, especially those that accreted in the outer disk. This potentially explains the discovery of refractory objects with low initial ²⁶Al/²⁷Al ratios in comets. Our model also shows that the highest fraction of refractory materials in meteorites formed around the time that infall stopped. Thus, we suggest that the calcium‐aluminum‐rich inclusions in chondrites would be dominated by the population that formed during the transition from class I to class II stage of young stellar objects. This helps us to understand the meaning of t = 0 in solar system chronology. Moreover, our model offers a possible explanation for the existence of isotopic variations observed among refractory materials—that the anomalous materials formed before the collapse of the parent molecular cloud was complete.     

Mineralogy of new Antarctic achondrites with affinity to Lodran and a model of their evolution in an asteroid

Abstract— We studied five new Antarctic achondrites, MacAlpine Hills (MAC) 88177, Yamato (Y)74357, Y75274, Y791491 and Elephant Moraine (EET)84302 by mineralogical techniques to gain a better understanding of the mineral assemblages of a group of meteorites with an affinity to Lodran (stony-iron meteorite) and their formation processes. This group is being called lodranites. These meteorites contain major coarse-grained orthopyroxene (Opx) and olivine as in Lodran and variable amounts of FeNi metal and troilite etc. MAC88177 has more augite and less FeNi than Lodran; Y74357 has more olivine and contains minor augite; Y791491 contains in addition plagioclase. EET84302 has an Acapulco-like chondritic mineral assembladge and is enriched in FeNi metal and plagioclase, but one part is enriched in Opx and chromite. The EET84302 and MAC88177 Opx crystals have dusty cores as in Acapulco. EET84302 and Y75274 are more Mg-rich than other members of the lodranite group, and Y74357 is intermediate. Since these meteorites all have coarse-grained textures, similar major mineral assemblages, variable amounts of augite, plagioclase, FeNi metal, chromite and olivine, we suggest that they are related and are linked to a parent body with modified chondritic compositions. The variability of the abundances of these minerals are in line with a proposed model of the surface mineral assemblages of the S asteroids. The mineral assemblages can best be explained by differing degrees of loss or movements of lower temperature partial melts and recrystallization, and reduction. A portion of EET84302 rich in metal and plagioclase may represent a type of component removed from the lodranite group meteorites. Y791058 and Caddo County, which were studied for comparison, are plagioclase-rich silicate inclusions in IAB iron meteorites and may have been derived by a similar process but in a different body.     

Petrography and mineralogy of the ungrouped type 3 carbonaceous chondrite Dar al Gani 978

Dar al Gani (DaG) 978 is an ungrouped type 3 carbonaceous chondrite. In this study, we report the petrography and mineralogy of Ca,Al‐rich inclusions (CAI), amoeboid olivine aggregates (AOAs), chondrules, mineral fragments, and the matrix in DaG 978. Twenty‐seven CAIs were found: 13 spinel‐diopside‐rich inclusions, 2 anorthite‐rich inclusions, 11 spinel‐troilite‐rich inclusions, and 1 spinel‐melilite‐rich inclusion. Most CAIs have a layered texture that indicates a condensation origin and are most similar to those in R chondrites. Compound chondrules represent a high proportion (approximately 8%) of chondrules in DaG 978, which indicates a local dusty chondrule‐forming region and multiple heating events. Most spinel and olivine in DaG 978 are highly Fe‐rich, which corresponds to a petrologic type of >3.5 and a maximum metamorphic temperature of approximately 850–950 K. This conclusion is also supported by other observations in DaG 978: the presence of coarse inclusions of silicate and phosphate in Fe‐Ni metal, restricted Ni‐Co distributions in kamacite and taenite, and low S concentrations in the matrix. Mineralogic records of iron‐alkali‐halogen metasomatism, such as platy and porous olivine, magnetite, hedenbergite, nepheline, Na‐rich in CAIs, and chlorapatite, are present, but relatively limited, in DaG 978. The fine‐grained, intergrowth texture of spinel‐troilite‐rich inclusions was probably formed by reaction between pre‐existing Al‐rich silicates and shock‐induced, high‐temperature S‐rich gas on the surface of the parent body of DaG 978. A shock‐induced vein is present in the matrix of DaG 978, which indicates that the parent body of DaG 978 at least experienced a shock event with a shock stage up to S3.     

MINERALOGY OF THE BOCAIUVA IRON METEORITE: A PRELIMINARY STUDY

The Bocaiuva iron contains 10 to 15% by volume of silicate inclusions which are surrounded by kamacite (6.5 wt % Ni). The metal shows a Widmanstätten pattern in metal areas devoid of silicates; taenite evolved in plessite fields. The silicate inclusions occur as nodules, and as irregular or chain-like aggregates in which olivine may be rounded or faceted. The magnesian silicates (forsterite, enstatite, diopside) are similar in composition to those of the group IAB irons, whereas the interstitial plagioclase is much more calcic (An 50) than that usually found. Iron sulfide occurs as pyrrhotite and contains 1–2 wt% Cu. Chromite and euhedral magnetite are accessory phases always associated with pyrrhotite. Some patches of pyrrhotite enclose rounded chromite and small plagioclase crystals displaying compositions different from those of the ground mass of the inclusions. Schreibersite shows a compositional variability. This preliminary study underlines the unusual nature of Ms iron and raises several questions concerning the genetic relations between silicates, sulfide and metal, and the thermal history of the whole material.     

Contribution of early impact events to metal‐silicate separation,thermal annealing,and volatile redistribution: Evidence in the Pułtusk H chondrite

Three‐dimensional X‐ray tomographic reconstructions and petrologic studies reveal voluminous accumulations of metal in Pu?tusk H chondrite. At the contact of these accumulations, the chondritic rock is enriched in troilite. The rock contains plagioclase‐rich bands, with textures suggesting crystallization from melt. Unusually large phosphates are associated with the plagioclase and consist of assemblages of merrillite, and fluorapatite and chlorapatite. The metal accumulations were formed by impact melting, rapid segregation of metal‐sulfide melt and the incorporation of this melt into the fractured crater basement. The impact most likely occurred in the early evolution of the H chondrite parent body, when post‐impact heat overlapped with radiogenic heat. This enabled slow cooling and separation of the metallic melt into metal‐rich and sulfide‐rich fractions. This led to recrystallization of chondritic rock in contact with the metal accumulations and the crystallization of shock melts. Phosphorus was liberated from the metal and subsumed by the silicate shock melt, owing to oxidative conditions upon slow cooling. The melt was also a host for volatiles. Upon further cooling, phosphorus reacted with silicates leading to the formation of merrillite, while volatiles partitioned into the residual halogen‐rich, dry fluid. In the late stages, the fluid altered merrillite to patchy Cl/F‐apatite. The above sequence of alterations demonstrates that impact during the early evolution of chondritic parent bodies might have contributed to local metal segregation and silicate melting. In addition, postshock conditions supported secondary processes: compositional/textural equilibration, redistribution of volatiles, and fluid alterations.     

Petrology of silicate inclusions in the Sombrerete ungrouped iron meteorite: Implications for the origins of IIE‐type silicate‐bearing irons

Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo_1–4Fs_25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An_70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.     

The pyroxene pallasites,Vermillion and Yamato 8451: Not quite a couple

Abstract— Two pallasites, Vermillion and Yamato (Y)‐8451, have been studied to obtain petrologic, trace element, and O‐isotopic data. Both meteorites contain low‐Ca and high‐Ca pyroxenes (<2% by volume) and have been dubbed “pyroxene pallasites.” Pyroxene occurs as large individual grains, as inclusions in olivine and in other pyroxene, and as grains along the edges of olivine. Symplectic overgrowths, sometimes found in Main Group and Eagle Station pallasites, are not seen in the pyroxene pallasites. Olivine compositions are Fa_10–12, similar to those of Main Group pallasites. Siderophile trace element data show that metal in the two meteorites have significantly differing compositions that are, for many elements, outside the range of the Main Group and Eagle Station pallasites. These compositions also differ from those of IAB and IIIAB iron meteorites. Rare earth element (REE) patterns in merrillite are similar to those seen in other pallasites, indicating formation by subsolidus reaction between metal and silicate, with the merrillite inheriting its pattern from the surrounding silicates. The O‐isotopic compositions of Vermillion and Y‐8451 are similar but differ from Main Group or Eagle Station pallasites, as well as other achondrite and primitive achondrite groups. Although Vermillion and Y‐8451 have similar mineralogy, pyroxene compositions, REE patterns, and O‐isotopic compositions, there is sufficient evidence to resist formally grouping these two meteorites. This evidence includes the texture of Vermillion, siderophile trace element data, and the presence of cohenite in Vermillion.     

Evolution of the winonaite parent body: Clues from silicate mineral trace element distributions

Abstract— We have measured the trace element compositions of individual plagioclase, pyroxene, and olivine grains in 6 different winonaites that span the range of textures and mineralogies observed in these meteorites. Textural evidence in these meteorites, including the presence of a plagioclase/clinopyroxene‐rich lithology and coarse‐grained olivine lithologies, suggests that they may have experienced some silicate partial melting. However, trace element distributions in these lithologies do not show any clear signatures for such an event. Pyroxene trace element compositions do exhibit systematic trends, with abundances generally lowest in Pontlyfni and highest in Winona. The fact that the same trends are present for both incompatible and compatible trace elements suggests, however, that the systematics are more likely the result of equilibration of minerals with initially heterogeneous and distinct compositions, rather than partial melting of a compositionally homogeneous precursor. The winonaites have experienced brecciation and mixing of lithologies, followed by varying degrees of thermal metamorphism on their parent body. These factors probably account for the variable bulk rare earth element (REE) patterns noted for these meteorites and may have led to re‐equilibration of trace elements in different lithologies.