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.     

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.     

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.     

Revisiting spectral parameters of silicate‐bearing meteorites

Abstract— Visible and near‐infrared reflectance spectra of a sample of silicate‐bearing meteorites have been used to evaluate the spectral parameters space defined in the pioneering work of Gaffey et al. (1993). The studied sample consisted of 91 ordinary chondrites, 47 basaltic achondrites, and 21 different laboratory mixtures obtained from the RELAB database. Our results indicate that the spectral parameter space, in particular the BAR versus band I center, is not suitable enough to identify the mineralogy of meteorites and asteroids. The grain size of the sample also appears as a very sensitive parameter and can play an important role in locating an object in the spectral parameter space. Finally, the application of our study to the question of a genetic link between V‐type asteroids and HED meteorites shows that these bodies plot in distinct regions in the BAR versus band I center space. This result further confirms that those spectral parameters cannot uniquely define the mineralogy of a sample.     

Portales Valley: Petrology of a metallic‐melt meteorite breccia

Abstract— Portales Valley (PV) is an unusual metal‐veined meteorite that has been classified as an H6 chondrite. It has been regarded either as an annealed impact melt breccia, as a primitive achondrite, or as a meteorite with affinities to silicated iron meteorites. We studied the petrology of PV using a variety of geochemical‐mineralogical techniques. Our results suggest that PV is the first well‐documented metallic‐melt meteorite breccia. Mineral‐chemical and other data suggest that the protolith to PV was an H chondrite. The composition of FeNi metal in PV is somewhat fractionated compared to H chondrites and varies between coarse vein and silicate‐rich portions. It is best modeled as having formed by partial melting at temperatures of ?940–1150 °C, with incomplete separation of solid from liquid metal. Solid metal concentrated in the coarse vein areas and S‐bearing liquid metal concentrated in the silicate‐rich areas, possibly as a result of a surface energy effect. Both carbon and phosphorus must have been scavenged from large volumes and concentrated in metallic liquid. Graphite nodules formed by crystallization from this liquid, whereas phosphate formed by reaction between P‐bearing metal and clinopyroxene components, depleting clinopyroxene throughout much of the meteorite and growing coarse phosphate at metal‐silicate interfaces. Some phosphate probably crystallized from P‐bearing liquids, but most probably formed by solid‐state reaction at ?975‐725 °C. Phosphate‐forming and FeO‐reduction reactions were widespread in PV and entailed a change in the mineralogy of the stony portion on a large scale. Portales Valley experienced protracted annealing from supersolidus to subsolidus temperatures, probably by cooling at depth within its parent body, but the main differences between PV and H chondrites arose because maximum temperatures were higher in PV. A combination of a relatively weak shock event and elevated pre‐shock temperatures probably produced the vein‐and‐breccia texture, with endogenic heating being the main heat source for melting, and with stress waves from an impact event being an essential trigger for mobilizing metal. Portales Valley is best classified as an H7 metallic‐melt breccia of shock stage S1. The meteorite is transitional between more primitive (chondritic) and evolved (achondrite, iron) meteorite types and offers clues as to how differentiation could have occurred in some asteroidal bodies.     

Petrology of magmatic silicate inclusions in the Allan Hills 77005 lherzolitic shergottite

Abstract— Magmatic inclusions occur in both chadacrystic olivine and oikocrystic pigeonite in ALH 77005 but are different from each other. Magmatic inclusions in olivine consist mainly of aluminous pyroxenes, intergrowths of plagioclase and silica, silica-predominant glass, and rhyodacitic glass, with minor amounts of chromite, spinel, pyrrhotite, and whitlockite. Those in pigeonite consist mainly of aluminous pyroxenes, nonaluminous ferroan pyroxenes, kaersutite, spinel, and K-rich trachytic glass, with minor amounts of pyrrhotite and whitlockite. The magmatic inclusions in chadacrystic olivine formed from trapped melts that were basaltic, apparently dry and crystallized additional olivine metastably. The basaltic magma, with entrained olivine, experienced magma mixing with K-rich and wet magmas, or assimilation of such crustal rocks, in the early to middle stages of the crystallization sequence of ALH 77005 during crystallization of chadacrystic olivine prior to precipitation of oikocrystic pigeonite. However the amount of mixed magmas or assimilated rocks was minor in comparison to the basaltic magma. Crystallization of pigeonite, augite, and plagioclase in the host lithologies took place in a shallow magma reservoir under an open-system condition, and the pigeonite trapped basaltic andesite to trachyandesitic melts, which resulted in magmatic inclusions in oikocrystic pigeonite. The magmatic inclusions in both olivine and pigeonite were formed under a rapid-cooling condition, resulting in a variety of inclusions. Kaersutite in magmatic inclusions in oikocrystic pigeonite crystallized under a closed-system wet condition during the late-stage crystallization of the inclusions.     

Replacement of glass in the Nakhla meteorite by berthierine: Implications for understanding the origins of aluminum‐rich phyllosilicates on Mars

A scanning and transmission electron microscope study of aluminosilicate glasses within melt inclusions from the Martian meteorite Nakhla shows that they have been replaced by berthierine, an aluminum‐iron serpentine mineral. This alteration reaction was mediated by liquid water that gained access to the glasses along fractures within enclosing augite and olivine grains. Water/rock ratios were low, and the aqueous solutions were circumneutral and reducing. They introduced magnesium and iron that were sourced from the dissolution of olivine, and exported alkalis. Berthierine was identified using X‐ray microanalysis and electron diffraction. It is restricted in its occurrence to parts of the melt inclusions that were formerly glass, thus showing that under the ambient physico‐chemical conditions, the mobility of aluminum and silicon were low. This discovery of serpentine adds to the suite of postmagmatic hydrous silicates in Nakhla that include saponite and opal‐A. Such a variety of secondary silicates indicates that during aqueous alteration compositionally distinct microenvironments developed on sub‐millimeter length scales. The scarcity of berthierine in Nakhla is consistent with results from orbital remote sensing of the Martian crust showing very low abundances of aluminum‐rich phyllosilicates.     

The formation of IIE iron meteorites investigated by the chondrule‐bearing Mont Dieu meteorite

A 435 kg piece of the Mont Dieu iron meteorite (MD) contains cm‐sized silicate inclusions. Based on the concentration of Ni, Ga, Ge, and Ir (8.59 ± 0.32 wt%, 25.4 ± 0.9 ppm, 61 ± 2 ppm, 7.1 ± 0.4 ppm, respectively) in the metal host, this piece can be classified as a IIE nonmagmatic iron. The silicate inclusions possess a chondritic mineralogy and relict chondrules occur throughout the inclusions. Major element analysis, oxygen isotopic analysis (Δ¹⁷O = 0.71 ± 0.02‰), and mean Fa and Fs molar contents (Fa_{15.7 ± 0.4} and Fs_{14.4 ± 0.5}) indicate that MD originated as an H chondrite. Because of strong similarities with Netschaëvo IIE, MD can be classified in the most primitive subgroup of the IIE sequence. ⁴⁰Ar/³⁹Ar ages of 4536 ± 59 Ma and 4494 ± 95 Ma obtained on pyroxene and plagioclase inclusions show that MD belongs to the old (~4.5 Ga) group of IIE iron meteorites and that it has not been perturbed by any subsequent heating event following its formation. The primitive character of MD sheds light on the nature of its formation process, its thermal history, and the evolution of its parent body.     

Remelting of refractory inclusions in the chondrule‐forming regions: Evidence from chondrule‐bearing type C calcium‐aluminum‐rich inclusions from Allende

Abstract— We describe the mineralogy, petrology, oxygen, and magnesium isotope compositions of three coarse‐grained, igneous, anorthite‐rich (type C) Ca‐Al‐rich inclusions (CAIs) (ABC, TS26, and 93) that are associated with ferromagnesian chondrule‐like silicate materials from the CV carbonaceous chondrite Allende. The CAIs consist of lath‐shaped anorthite (An₉₉), Cr‐bearing Al‐Ti‐diopside (Al and Ti contents are highly variable), spinel, and highly åkermanitic and Na‐rich melilite (Åk_63–74, 0.4–0.6 wt% Na₂O). TS26 and 93 lack Wark‐Lovering rim layers; ABC is a CAI fragment missing the outermost part. The peripheral portions of TS26 and ABC are enriched in SiO₂ and depleted in TiO₂ and Al₂O₃ compared to their cores and contain relict ferromagnesian chondrule fragments composed of forsteritic olivine (Fa_6–8) and low‐Ca pyroxene/pigeonite (Fs₁Wo_1–9). The relict grains are corroded by Al‐Ti‐diopside of the host CAIs and surrounded by haloes of augite (Fs_0.5Wo_30–42). The outer portion of CAI 93 enriched in spinel is overgrown by coarse‐grained pigeonite (Fs_0.5–2Wo_5–17), augite (Fs_0.5Wo_38–42), and anorthitic plagioclase (An₈₄). Relict olivine and low‐Ca pyroxene/pigeonite in ABC and TS26, and the pigeonite‐augite rim around 93 are ¹⁶O‐poor (Δ17O ～ ?1‰ to ?8‰). Spinel and Al‐Ti‐diopside in cores of CAIs ABC, TS26, and 93 are ¹⁶O‐enriched (Δ17O down to ?20‰), whereas Al‐Ti‐diopside in the outer zones, as well as melilite and anorthite, are ¹⁶O‐depleted to various degrees (Δ17O = ?11‰ to 2‰). In contrast to typical Allende CAIs that have the canonical initial ²⁶Al/²⁷Al ratio of ～5 × 10^?5 ABC, 93, and TS26 are ²⁶Al‐poor with (²⁶Al/²⁷Al)₀ ratios of (4.7 ± 1.4) × 10^?6 (1.5 ± 1.8) × 10^?6 <1.2 × 10^?6 respectively. We conclude that ABC, TS26, and 93 experienced remelting with addition of ferromagnesian chondrule silicates and incomplete oxygen isotopic exchange in an ¹⁶O‐poor gaseous reservoir, probably in the chondrule‐forming region. This melting episode could have reset the ²⁶Al‐²⁶Mg systematics of the host CAIs, suggesting it occurred ～2 Myr after formation of most CAIs. These observations and the common presence of relict CAIs inside chondrules suggest that CAIs predated formation of chondrules.     

Trace element studies of silicate‐rich inclusions in the Guin (UNGR) and Kodaikanal (IIE) iron meteorites

Abstract— A devitrified glass inclusion from the Guin (UNGR) iron consists of cryptocrystalline feldspars, pyroxenes, and silica and is rich in SiO₂, Al₂O₃, and Na₂O. It contains a rutile grain and is in contact with a large Cl apatite. The latter is very rich in rare earth elements (REEs) (～80 × CI), which display a flat abundance pattern, except for Eu and Yb, which are underabundant. The devitrified glass is very poor in REEs (<0.1 × CI), except for Eu and Yb, which have positive abundance anomalies. Devitrified glass and Cl apatite are out of chemical equilibrium and their complementary REE patterns indicate a genesis via condensation under reducing conditions. Inclusion 1 in the Kodaikanal (IIE) iron consists of glass only, whereas inclusion 2 consists of clinopyroxene, which is partly overgrown by low‐Ca pyroxene, and apatite embedded in devitrified glass. All minerals are euhedral or have skeletal habits indicating crystallization from the liquid precursor of the glass. Pyroxenes and the apatite are rich in trace elements, indicating crystallization from a liquid that had 10–50 × CI abundances of REEs and refractory lithophile elements (RLEs). The co‐existing glass is poor in REEs (～0.1–1 × CI) and, consequently, a liquid of such chemical composition cannot have crystallized the phenocrysts. Glasses have variable chemical compositions but are rich in SiO₂, Al₂O₃, Na₂O, and K₂O as well as in HFSEs, Be, B, and Rb. The REE abundance patterns are mostly flat, except for the glass‐only inclusion, which has heavy rare earth elements (HREEs) > light rare earth elements (LREEs) and deficits in Eu and Yb—an ultrarefractory pattern. The genetic models suggested so far cannot explain what is observed and, consequently, we offer a new model for silicate inclusion formation in IIE and related irons. Nebular processes and a relationship with E meteorites (Guin) or Ca‐Al‐rich inclusions (CAIs) (Kodaikanal) are indicated. A sequence of condensation (CaS, TiN or refractory pyroxene‐rich liquids) and vapor‐solid elemental exchange can be identified that took place beginning under reducing and ending at oxidizing conditions (phosphate, rutile formation, alkali and Fe²⁺ metasomatism, metasomatic loss of REEs from glass).     

Petrology and mineralogy of volcanic glass in meteorite Northwest Africa 11801: Implications for their petrogenesis

The study of lunar magma evolution holds significant importance within the scientific community due to its relevance in understanding the Moon's thermal and geological history. However, the intricate task of unraveling the history of early volcanic activity on the Moon is hindered by the high flux of impactors, which have substantially changed the morphology of pristine volcanic constructs. In this study, we focus on a unique volcanic glass found in the lunar meteorite Northwest Africa 11801. This kind of volcanic glass is bead-like in shape and compositionally similar to the Apollo-14 and Apollo-17 very low-Ti glass. Our research approach involves conducting a comprehensive analysis of the petrology and mineralogy of the volcanic glass, coupled with multiple thermodynamic modeling techniques. Through the investigation, we aim to shed light on the petrological characteristics and evolutionary history of the glass. The results indicate that the primitive magma of the glass was created at 1398–1436°C and 8.3–11.9 kbar (166–238 km) from an olivine+orthopyroxene mantle source region. Then, the magma ascended toward the surface along a non-adiabatic path with an ascent rate of ~40 m s⁻¹ or 0.2 MPa s⁻¹. During the magma ascent, only olivine crystallized and the onset of magma eruption occurred at ~1320–1343°C. Finally, the glass cooled rapidly on the lunar surface with a cooling rate ranging between 20 and 200 K min⁻¹. Considerable evidence from petrology, mineralogy, cooling rate, and the eruption rate of the glass beads strongly supports the occurrence of ancient explosive volcanism on the Moon.     

Northwest Africa 1500: Plagioclase‐bearing monomict ureilite or ungrouped achondrite?

Abstract— Northwest Africa (NWA) 1500 is an ultramafic meteorite dominated by coarse (?100–500 μm) olivine (95–96%), augite (2–3%), and chromite (0.6–1.6%) in an equilibrated texture. Plagioclase (0.7–1.8%) occurs as poikilitic grains (up to ?3 mm) in vein‐like areas that have concentrations of augite and minor orthopyroxene. Other phases are Cl‐apatite, metal, sulfide, and graphite. Olivine ranges from Fo 65–73, with a strong peak at Fo 68–69. Most grains are reversezoned, and also have ?10–30 μm reduction rims. In terms of its dominant mineralogy and texture, NWA 1500 resembles the majority of monomict ureilites. However, it is more ferroan than known ureilites (Fo ≥75) and other mineral compositional parameters are out of the ureilite range as well. Furthermore, neither apatite nor plagioclase have ever been observed, and chromite is rare in monomict ureilites. Nevertheless, this meteorite may be petrologically related to the rare augite‐bearing ureilites and represent a previously unsampled part of the ureilite parent body (UPB). The Mn/Mg ratio of its olivine and textural features of its pyroxenes are consistent with this interpretation. However, its petrogenesis differs from that of known augite‐bearing ureilites in that: 1) it formed under more oxidized conditions; 2) plagioclase appeared before orthopyroxene in its crystallization sequence; and 3) it equilibrated to significantly lower temperatures (800–1000 °C, from two‐pyroxene and olivine‐chromite thermometry). Formation under more oxidized conditions and the appearance of plagioclase before orthopyroxene could be explained if it formed at a greater depth on the UPB than previously sampled. However, its significantly different thermal history (compared to ureilites) may more plausibly be explained if it formed on a different parent body. This conclusion is consistent with its oxygen isotopic composition, which suggests that it is an ungrouped achondrite. Nevertheless, the parent body of NWA 1500 may have been compositionally and petrologically similar to the UPB, and may have had a similar differentiation history.     

The origins of I‐type spherules and the atmospheric entry of iron micrometeoroids

The Earth's extraterrestrial dust flux includes a wide variety of dust particles that include FeNi metallic grains. During their atmospheric entry iron micrometeoroids melt and oxidize to form cosmic spherules termed I‐type spherules. These particles are chemically resistant and readily collected by magnetic separation and are thus the most likely micrometeorites to be recovered from modern and ancient sediments. Understanding their behavior during atmospheric entry is crucial in constraining their abundance relative to other particle types and the nature of the zodiacal dust population at 1 AU. This article presents numerical simulations of the atmospheric entry heating of iron meteoroids to investigate the abundance and nature of these materials. The results indicate that iron micrometeoroids experience peak temperatures 300–800 K higher than silicate particles explaining the rarity of unmelted iron particles which can only be present at sizes of <50 μm. The lower evaporation rates of liquid iron oxide leads to greater survival of iron particles compared with silicates, which enhances their abundance among micrometeorites by a factor of 2. The abundance of I‐types is shown to be broadly consistent with the abundance and size of metal in ordinary chondrites and the current day flux of ordinary chondrite‐derived MMs arriving at Earth. Furthermore, carbonaceous asteroids and cometary dust are suggested to make negligible contributions to the I‐type spherule flux. Events involving such objects, therefore, cannot be recognized from I‐type spherule abundances in the geological record.     

Oxygen isotopic zoning of reversely zoned melilite crystals in a fluffy type A Ca‐Al‐rich inclusions from the Vigarano meteorite

Abstract– The oxygen isotopic microdistributions within melilite measured using in situ secondary ion mass spectrometry correspond to the chemical zoning profiles in single melilite crystals of a fluffy type A Ca‐Al‐rich inclusions (CAIs) of reduced CV3 Vigarano meteorite. The melilite crystals show chemical reverse zoning within an individual single crystal from the åkermanite‐rich core to the åkermanite‐poor rim. The composition changes continuously with the crystal growth. The zoning structures suggest that the melilite grew in a hot nebular gas by condensation with decreasing pressure. The oxygen isotopic composition of melilite also changes continuously from ¹⁶O‐poor to ¹⁶O‐rich with the crystal growth. These observations suggest that the melilite condensation proceeded with change consistent with an astrophysical setting around the inner edge of a protoplanetary disk where both ¹⁶O‐rich solar coronal gas and ¹⁶O‐poor dense protoplanetary disk gas could coexist. Fluffy type A CAIs could have been formed around the inner edge of the protoplanetary disk surrounding the early sun.     

An experimental study on kinetically‐driven precipitation of calcium‐magnesium‐iron carbonates from solution: Implications for the low‐temperature formation of carbonates in martian meteorite Allan Hills 84001

Abstract— Spherical carbonate globules of similar composition, size, and radial Ca‐, Mg‐, and Fe‐zonation to those in martian meteorite Allan Hills (ALH) 84001 were precipitated from Mg‐rich, supersaturated solutions of Ca‐Mg‐Fe‐CO₂‐H₂O at 150 °C. The supersaturated solutions (pH ? 6–7) were prepared at room temperature and contained in Teflon^TM‐lined stainless steel vessels, which were sealed and heated to 150 °C for 24 h. Experiments were also conducted at 25 °C and no globules comparable to those of ALH 84001 were precipitated. Instead, amorphous Fe‐rich carbonates were formed after 24 h and Mg‐Fe calcites formed after 96 h. These experiments suggest a possible low‐temperature inorganic origin for the carbonates in martian meteorite ALH 84001.     

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.     

Glass‐bearing inclusions in olivine of the Chassigny achondrite: Heterogeneous trapping at sub‐igneous temperatures

Abstract— Three types of glass‐bearing inclusions are present in olivine and chromite of the Chassigny achondrite: pure glass, monocrystal (glass plus a single mineral grain), and multiphase (glass plus a variety of minerals) inclusions. The occurrence, texture, and mineralogy of these inclusions and the chemical composition of the glass suggest an origin by heterogeneous trapping of these phases. The glass is rich in SiO₂, Al₂O₃, Na₂O, K₂O; and poor in MgO, FeO, and CaO; and contains appreciable amounts of Cl. The compositional variability of the glass is independent of the mineral content of the inclusions. Heating experiments with final temperatures of 900, 1000, and 1200 °C were performed with Chassigny inclusions for the first time. The glass of the heated inclusions has a chemical composition similar to that of unheated inclusions. This situation suggests that the glass cannot be a residual melt but rather is an independent component that was trapped with or without mineral phases. The extreme heterogeneity in alkali contents, and in particular Rb and Sr contents, also suggests precipitation and mixing of solid precursors. The most Rb‐rich glasses have near‐chondritic Rb/Sr ratios, possibly indicating a chondritic source for their precursor(s). None of the inclusions contain bubbles like those of typical melt inclusions in terrestrial igneous minerals. Furthermore, many inclusions are at the center of radial cracks in the host olivine, which indicates development of an overpressure within the inclusions at some time. A volume increase of the inclusions could have been achieved by differential thermal expansion of the content of the inclusion during a heating event. That mechanism requires bubble‐free and solid preheating inclusion contents. These features are incompatible with an origin of the inclusions by trapping of a silicate melt and point toward heterogeneous trapping of solid phases. The first N analyses performed in Chassigny glass‐bearing inclusions by nuclear reaction analysis (NRA) revealed high and variable N contents of the glass, which suggests trapping of a solid precursor (presumably at relatively low temperatures) from a fluid rather than a melt. In conclusion, the glass‐bearing inclusions in Chassigny olivine are not residuals after a closed‐system evolution of a trapped melt, but rather heterogeneously trapped precipitates of a fluid that existed during formation of Chassigny constituents. Consequently, it is very unlikely that the host olivine has an igneous origin.     

Matrix and whole‐rock fractionations in the Acfer 094 type 3.0 ungrouped carbonaceous chondrite

Abstract– We used the electron microprobe to study matrix in the ungrouped type 3.0 carbonaceous chondrite Acfer 094 using 7 × 7‐point, focused‐beam arrays; data points attributable to mineral clasts were discarded. The grid areas show resolvable differences in composition, but differences are less pronounced than we observed in studies of CR2 LaPaz Icefield (LAP) 02342 (Wasson and Rubin [2009]) and CO3.0 Allan Hills A77307 (Brearley [1993]). A key question is why Acfer shows an anomalously uniform composition of matrix compared with these other carbonaceous chondrites. Both whole‐rock and matrix samples of Acfer 094 show enhancements of Ca and K; it appears that these reflect contamination during hot desert weathering. By contrast, the whole‐rock abundance of Na is low. Although weathering effects are responsible for some fractionations, it appears that nebular effects are also resolvable in matrix compositions in Acfer 094. As with LAP 02342, we infer that the observed differences among different areas were inherited from the solar nebula and may have been carried by porous chondrules that experienced low (about 20%) degrees of melting. Acfer 094 has been comminuted by one or more impact events that may also have caused volatile loss. Thus, despite preserving evidence (e.g., an exceptionally high content of presolar SiC) implying a high degree of pristinity, Acfer 094 is far from pristine in other respects. This evidence of comminution and an O‐isotopic composition similar to values measured in metamorphosed CM chondrites suggest that Acfer was hydrated before being outgassed by the inferred impact event. Convection within the plume associated with the impact event probably also contributed to the homogenization of the Acfer 094 matrix.     

Forsterite‐bearing type B refractory inclusions from CV3 chondrites: From aggregates to volatilized melt droplets

Abstract– Detailed petrologic and oxygen isotopic analysis of six forsterite‐bearing Type B calcium‐aluminum‐rich inclusions (FoBs) from CV3 chondrites indicates that they formed by varying degrees of melting of primitive precursor material that resembled amoeboid olivine aggregates. A continuous evolutionary sequence exists between those objects that experienced only slight partial melting or sintering through objects that underwent prolonged melting episodes. In most cases, melting was accompanied by surface evaporative loss of magnesium and silicon. This loss resulted in outer margins that are very different in composition from the cores, so much so that in some cases, the mantles contain mineral assemblages that are petrologically incompatible with those in the cores. The precursor objects for these FoBs had a range of bulk compositions and must therefore have formed under varying conditions if they condensed from a solar composition gas. Five of the six objects show small degrees of mass‐dependent oxygen isotopic fractionation in pyroxene, spinel, and olivine, consistent with the inferred melt evaporation, but there are no consistent differences among the three phases. Forsterite, spinel, and pyroxene are ¹⁶O‐rich with Δ¹⁷O ～ ?24‰ in all FoBs. Melilite and anorthite show a range of Δ¹⁷O from ?17‰ to ?1‰.     

Oxygen isotopic compositions and origins of calcium‐aluminum‐rich inclusions and chondrules

Abstract— Primary minerals in calcium‐aluminum‐rich inclusions (CAIs), Al‐rich and ferromagnesian chondrules in each chondrite group have δ¹⁸O values that typically range from ?50 to +5%0. Neglecting effects due to minor mass fractionations, the oxygen isotopic data for each chondrite group and for micrometeorites define lines on the three‐isotope plot with slopes of 1.01 ± 0.06 and intercepts of ?2 ± 1. This suggests that the same kind of nebular process produced the ¹⁶O variations among chondrules and CAIs in all groups. Chemical and isotopic properties of some CAIs and chondrules strongly suggest that they formed from solar nebula condensates. This is incompatible with the existing two‐component model for oxygen isotopes in which chondrules and CAIs were derived from heated and melted ¹⁶O‐rich presolar dust that exchanged oxygen with ¹⁶O‐poor nebular gas. Some FUN CAIs (inclusions with isotope anomalies due to fractionation and unknown nuclear effects) have chemical and isotopic compositions indicating they are evaporative residues of presolar material, which is incompatible with ¹⁶O fractionation during mass‐independent gas phase reactions in the solar nebula. There is only one plausible reason why solar nebula condensates and evaporative residues of presolar materials are both enriched in ¹⁶O. Condensation must have occurred in a nebular region where the oxygen was largely derived from evaporated ¹⁶O‐rich dust. A simple model suggests that dust was enriched (or gas was depleted) relative to cosmic proportions by factors of ～10 to >50 prior to condensation for most CAIs and factors of 1–5 for chondrule precursor material. We infer that dust‐gas fractionation prior to evaporation and condensation was more important in establishing the oxygen isotopic composition of CAIs and chondrules than any subsequent exchange with nebular gases. Dust‐gas fractionation may have occurred near the inner edge of the disk where nebular gases accreted into the protosun and Shu and colleagues suggest that CAIs formed.