Igneous Rims Research Articles

Evaluation of petrologic evidence for high partial pressures of SiO(g) in the solar nebula

AbstractAlthough they cannot be ruled out, high partial pressures of SiO(g) in the solar nebula are not required to produce various petrologic features of chondrules. These features include the low‐Ca‐pyroxene‐rich margins of type‐IAB chondrules, high concentrations of SiO2 and Na2O in mesostasis near the surface of some chondrules in LL3.0 Semarkona, and silica‐rich igneous rims around many type‐I chondrules in CR chondrites. It is a misconception that low‐Ca pyroxene phenocrysts are restricted mainly to the periphery of type‐IAB chondrules; instead, they are widely distributed in most of these chondrules. Type‐IAB chondrules can be modeled as having formed by remelting of type‐IB chondrules that contained relict olivine grains derived from disrupted type‐IA chondrules. Semarkona chondrule mesostases that show increased concentrations of SiO2 and Na2O from the core to the rim were probably affected by parent‐body aqueous alteration. The silica‐rich igneous rims around many type‐I chondrules in CR chondrites may have formed by melting of pyroxene‐rich dust aggregates that had been previously enriched in Na, K, and Mn derived from volatilized chondrules.

A new type of oxidized and pre-irradiated micrometeorite

This paper investigates the mineralogy and noble gas composition of a unique micrometeorite from the Transantarctic Mountains, #45c.29. The magnetite rim and the particle interior with olivine, pyroxene and magnetite relict grains (30–250 µm in size) set in a vesicular mesostasis are typical features of coarse-grained, partially melted micrometeorites. Particle #45c.29 stands out from other micrometeorites of this type by the texture of the mesostasis made of abundant plagioclase and augite laths, the remarkably high Ni contents in magnetite and olivine relict grains, and by the similarly high abundance of cosmogenic noble gases (21Necos up to 1.62 × 10−7 cm3 STP/g and 38Ar up to 7.2 × 10−8 cm3 STP/g). The high Ni content of Fa26 olivine relict grains (NiO ∼ 0.65 wt%), the high Ni (NiO ∼ 0.8 wt%) and Ti (TiO2 ∼ 0.3 wt%) contents of magnetite relicts, and the oxygen isotope composition of a sample of the particle (δ18O ∼ 2.3‰, δ17O ∼ −1.5‰), suggest a parentage with rare equilibrated CK chondrites. Pyroxene and plagioclase are not expected to crystallize during atmospheric entry of micrometeoroids. Their occurrence in #45c.29 may be explained by the Ca-, Al- and Na- rich composition of its precursor – in agreement with the high abundance of plagioclase reported in the matrix of CK chondrites – if combined with a relatively low cooling rate and, therefore, unusual atmospheric entry parameters (velocity/angle) of the micrometeoroid. Given these specific entry parameters, the particle has recorded unique information on mineralogical and textural transformations of micrometeoroids during atmospheric entry, with solid-state oxidation of the olivine relict grains in the igneous rim, and partial melting of relict mineral phases and relict/melt reactions in the particle interior. The cosmogenic 21Ne/22Ne ratio of 0.94 ± 0.02 is incompatible with major production by cosmogenic ray irradiation of a small particle in space. We propose that micrometeorite #45c.29 mostly records an earlier irradiation stage, in a meteoroid or more likely near the surface (<20 cm in depth) of an asteroid. In contrast, most of the other unmelted and scoriaceous micrometeorites analyzed for noble gases – if coming from asteroidal sources of the Main Belt – seem to have sampled deeper parts of their parent body, where they were shielded from cosmic rays and from where they were excavated during high-energy disruptive processes.

High-temperature rims around calcium–aluminum-rich inclusions from the CR, CB and CH carbonaceous chondrites

We describe the mineralogy, petrology and oxygen isotopic compositions of high-temperature rims around mineralogically pristine calcium–aluminum-rich inclusions (CAIs) from the CR, CB and CH carbonaceous chondrites. In CR chondrites, nearly all CAIs are surrounded by single- or multi-layered rims composed of CAI-like minerals; relict CAIs inside chondrules in which the rims were resorbed by the host chondrule melt (Aléon et al., 2002; Makide et al., 2009) are the only exception. A complete multi-layered rim sequence (from inside outward: spinel+hibonite+perovskite→melilite→anorthite replacing melilite→Al-diopside→forsterite) is rarely observed; Al-diopside±forsterite rims are more common. The CR CAIs and all rim layers are uniformly 16O-rich (Δ17O ∼−24‰), indicating formation in a 16O-rich gaseous reservoir. The mineralogy, petrology and 16O-rich compositions of these rims suggest formation by evaporation/condensation, melting (?), and thermal annealing in the formation region of the host CAIs. We define such rims as the primordial Wark–Lovering (WL) rims.In CH chondrites, most CAIs are uniformly 16O-rich and surrounded by the primordial WL rims. One of the 16O-rich CAIs is surrounded by an anorthite–Al-diopside WL rim showing a range of Δ17O values, from ∼−24‰ to ∼−6‰; Δ17O decreases towards the CAI core. We infer that this rim experienced incomplete melting and O-isotope exchange in an 16O-poor nebular gas, most likely during chondrule formation.Most CAIs in CB chondrites and about 10% of CAIs in CH chondrites are uniformly 16O-depleted igneous inclusions; Δ17O values between individual CAIs vary from ∼−12‰ to ∼−5‰. These CAIs have diverse mineralogies (grossite-rich, hibonite-rich, melilite-rich, spinel-rich, and Al,Ti-diopside±forsterite-rich), but are surrounded by the mineralogically similar igneous rims composed of ±melilite, Al-diopside and Ca-rich forsterite (0.5–1.4wt% CaO). The igneous rims and the host igneous CAIs have identical (within uncertainties of our SIMS measurements) O-isotope compositions, suggesting that they crystallized from isotopically similar, but chemically distinct melts. We suggest that the uniformly 16O-depleted igneous rims around the uniformly 16O-depleted igneous CAIs in CB and CH chondrites formed during melting of pre-existing CAIs in an impact-generated plume invoked for the origin of CB chondrites (Krot et al., 2005), followed by O-isotope exchange with an 16O-poor plume gas (Δ17O ∼−2‰), condensation of gaseous SiO and Mg into CAI melt, and its subsequent crystallization.We conclude that high-temperature rims around CAIs from CR, CH and CB chondrites recorded thermal processing in gaseous reservoirs with different oxygen isotopic compositions. In contrast to the isotopically heterogeneous WL rims around CV CAIs, our data provide no evidence that CAIs were transported between 16O-rich and 16O-poor gaseous reservoirs multiple times. We suggest instead that oxygen-isotope heterogeneity in the CV WL rims resulted from a fluid-rock interaction on the CV parent asteroid.

Calcium–aluminum-rich inclusions recycled during formation of porphyritic chondrules from CH carbonaceous chondrites

We report on the mineralogy, petrography, and O-isotope compositions of ∼60 Ca, Al-rich inclusions (CAIs) incompletely melted during formation of porphyritic chondrules from the CH metal-rich carbonaceous chondrites and Isheyevo (CH/CB). These include (i) relict polymineralic CAIs in porphyritic chondrules, (ii) CAIs surrounded by chondrule-like igneous rims, (iii) igneous pyroxene-rich and Type C-like CAIs, and (iv) plagioclase-rich chondrules with clusters of relict spinel grains. 26Al–26Mg systematics were measured in 10 relict CAIs and 11 CAI-bearing plagioclase-rich chondrules. Based on the mineralogy, the CH CAIs incompletely melted during chondrule formation can be divided into grossite-rich (n=13), hibonite-rich (n=11), spinel±melilite-rich (n=33; these include plagioclase-rich chondrules with clusters of relict spinel grains) types. Mineralogical observations indicate that these CAIs were mixed with different proportions of ferromagnesian silicates and experienced incomplete melting and gas–melt interaction during chondrule formation. These processes resulted in partial or complete destruction of the CAI Wark–Lovering rims, replacement of melilite by Na-bearing plagioclase, and dissolution and overgrowth of nearly end-member spinel by chromium- and iron-bearing spinel. Only two relict CAIs and two CAI-bearing chondrules show resolvable excess of radiogenic 26Mg; the inferred initial 26Al/27Al ratios are (1.7±1.3)×10–6, (3.7±3.1)×10–7, (1.9±0.9)×10–6 and (4.9±2.6)×10–6. There is a large range of Δ17O among the CH CAIs incompletely melted during chondrule formation, from ∼−37‰ to ∼−5‰; the unmelted minerals in individual CAIs, however, are isotopically uniform and systematically 16O-enriched relative to the host chondrules and chondrule-like igneous rims, which have Δ17O ranging from ∼−7‰ to ∼+4‰. Most of the CH CAIs incompletely melted during chondrule formation are mineralogically and isotopically similar to the CH CAIs surrounded by Wark–Lovering rims and apparently unaffected by chondrule melting. The mineralogy and O-isotope compositions of the CH CAI-bearing chondrules are similar to those of the CH porphyritic chondrules without relict CAIs.We conclude that CH porphyritic chondrules formed by incomplete melting of isotopically diverse solid precursors, including mineralogically and isotopically unique CAIs commonly observed only in CH chondrites. Therefore, the CH porphyritic chondrules must have formed in a distinct disk region, where the CH CAIs were present at the time of chondrule formation. Because most CH CAIs avoided chondrule melting, we infer that chondrule formation was highly localized. These observations preclude formation of CH porphyritic chondrules by splashing of molten planetesimals, by impact processing of differentiated planetesimals, and by large scale nebular shocks, e.g., shocks driven by disk gravitational instabilities or by X-ray flares. Instead, they are consistent with small-scale chondrule-forming mechanisms proposed in the literature, such as nebular processing of dust balls by bow shocks and by current sheets.

Chondrules in CK carbonaceous chondrites and thermal history of the CV–CK parent body

AbstractCK chondrites are the only group of carbonaceous chondrites with petrologic types ranging from 3 to 6. It is commonly reported than ~15 vol% of CK4–6 samples are composed of chondrules. The modal abundance of chondrules estimated here for 18 CK3–6 (including five CK3s) ranges from zero (totally recrystallized) to 50.5%. Although almost all chemically re‐equilibrated with the host matrix, we recognized in CK3s and Tanezrouft (Tnz) 057 (CK4) up to 85% of chondrules as former type I chondrules. Mean diameters of chondrules range from 0.22 to 1.05 mm for Karoonda (CK4) and Tnz 057 (CK4), respectively. Up to ~60% of chondrules in CK3–4 are surrounded by igneous rims (from ~20 μm to 2 mm width). Zoned olivines were found in unequilibrated chondrules from DaG 431 (CK3‐an), NWA 4724 (CK3.8), NWA 4423 (CK3.9), and Tnz 057 (CK4). We modeled Fe/Mg interdiffusion profiles measured in zoned olivines to evaluate the peak metamorphic temperatures and time scales of the CK parent body metamorphism, and proposed a two‐stage diffusion process in order to account for the position of inflection points situated within chondrules. Time scales inferred from Fe/Mg interdiffusion in olivine from unequilibrated chondrules are on the order of tens to a hundred thousand years (from 50 to 70,000 years for peak metamorphic temperatures of 1140 and 920 K, respectively). These durations are longer than what is commonly accepted for shock metamorphism and shorter than what is required for nuclide decay. Using the concept of a continuous CV–CK metamorphic series, which is reinforced by this study, we estimated peak metamorphic temperatures &lt;850 K for CV, 850–920 K for CK3, and 920–1140 K for CK4–6 chondrites considering a duration of 70,000 years.

Oxygen-isotope compositions of chondrule phenocrysts and matrix grains in Kakangari K-grouplet chondrite: Implication to a chondrule-matrix genetic relationship

To investigate a possible relationship between chondrules and matrix, we studied mineralogy, mineral chemistry, and in situ O-isotope compositions of chondrules, clastic matrix grains, and amoeboid olivine aggregates (AOAs) in the Kakangari K-grouplet chondrite. Most olivines and low-Ca pyroxenes in the Kakangari chondrules, matrix, and AOAs have similar magnesium-rich compositions, Fo∼95–97 (∼0.3–0.5wt% MnO) and En∼90–96, respectively. These rather uniform chemical compositions of the different chondritic components are likely due to partial Fe–Mg–Mn equilibration during thermal metamorphism experienced by the host meteorite. Oxygen-isotope compositions of olivine and low-Ca pyroxene grains in chondrules and matrix plot along a slope-1 line on a three O-isotope diagram and show a range from 16O-enriched composition similar to that of the Sun to 16O-depleted composition similar to the terrestrial O-isotope composition. Most olivines and low-Ca pyroxenes in chondrules are 16O-poor and plot on or close to the terrestrial mass-fractionation line (mean Δ17O values ±2 standard deviations: 0.0±0.8‰ and +0.2±0.9‰ for olivine and pyroxene, respectively), consistent with the previously reported compositions of bulk chondrules (Δ17O=−0.16±0.70‰). In addition to these 16O-poor grains, a coarse-grained igneous rim surrounding a porphyritic chondrule contains abundant 16O-rich relict olivines (Δ17O∼−24‰). Oxygen-isotope compositions of olivines and low-Ca pyroxenes in matrix show a bimodal distribution: 12 out of 13 olivine and 4 out of 17 pyroxene grains measured are similarly 16O-rich (Δ17O∼−23.5±2.9‰), others are similarly 16O-poor (Δ17O∼−0.1±1.7‰). Due to slow oxygen self-diffusion, olivines and low-Ca pyroxenes largely retained their original oxygen-isotope compositions. The nearly identical O-isotope compositions between the chondrule phenocrysts and the 16O-poor matrix grains suggest both chondrules and matrix of Kakangari sampled isotopically the same reservoirs. In addition, the presence of abundant 16O-rich grains in matrix and the chondrule igneous rim suggests both components acquired similar precursor inventories. These observations imply that chondrules and matrix in Kakangari are genetically related in the sense that material that formed matrix was one of the precursors of chondrules and chondrules and some fraction of matrix experienced the same thermal processing event. The 16O-enriched bulk matrix value compared to the bulk chondrules reported previously is likely due to presence of abundant 16O-rich grains in the Kakangari matrix.

MINERAL PROCESSING BY SHORT CIRCUITS IN PROTOPLANETARY DISKS

Meteoritic chondrules were formed in the early solar system by brief heating of silicate dust to melting temperatures. Some highly refractory grains (Type B calcium-aluminum-rich inclusions, CAIs) also show signs of transient heating. A similar process may occur in other protoplanetary disks, as evidenced by observations of spectra characteristic of crystalline silicates. One possible environment for this process is the turbulent magnetohydrodynamic flow thought to drive accretion in these disks. Such flows generally form thin current sheets, which are sites of magnetic reconnection, and dissipate the magnetic fields amplified by a disk dynamo. We suggest that it is possible to heat precursor grains for chondrules and other high-temperature minerals in current sheets that have been concentrated by our recently described short-circuit instability. We extend our work on this process by including the effects of radiative cooling, taking into account the temperature dependence of the opacity; and by examining current sheet geometry in three-dimensional, global models of magnetorotational instability. We find that temperatures above 1600 K can be reached for favorable parameters that match the ideal global models. This mechanism could provide an efficient means of tapping the gravitational potential energy of the protoplanetary disk to heat grains strongly enough to form high-temperature minerals. The volume-filling nature of turbulent magnetic reconnection is compatible with constraints from chondrule-matrix complementarity, chondrule-chondrule complementarity, the occurrence of igneous rims, and compound chondrules. The same short-circuit mechanism may perform other high-temperature mineral processing in protoplanetary disks such as the production of crystalline silicates and CAIs.

Compositional and petrographic similarities of CV and CK chondrites: A single group with variations in textures and volatile concentrations attributable to impact heating, crushing and oxidation

Greenwood et al. (2010) gathered data on O-isotopic and elemental compositions and reevaluated literature data for CV and CK chondrites. They concluded that these two chondrite groups originated on the same parent asteroid, with CK chondrites being metamorphosed CV chondrites (which are otherwise missing types 4 through 6). To test this interpretation we have gathered new instrumental neutron-activation-analysis (INAA) data for CV and CK chondrites and reexamined their petrographic features. The new INAA data like the older data show scatter attributable to weathering effects, but we conclude that the refractory lithophile abundances are the same in CV and CK, in agreement with the Greenwood et al. interpretation. Several volatile elements are significantly lower in CK than in CV chondrites. Among the elements we determine, the greatest difference between CV and CK is found for Br, for which the CV/CK ratio is ∼4; As and Sb are about 20% lower in CK than CV and smaller differences are observed for Zn, Ga and Se. It seems likely that volatiles were lost during impact-heating events that also provided the heat responsible for metamorphic recrystallization. Within statistical uncertainty, chondrules in CV and CK chondrites are the same size and have similar textural distributions. A significant petrographic difference between CK and CV chondrites cited by Kallemeyn et al. (1991) was the much higher percentage of igneous rims around CV chondrules. However, we now recognize that many chondrules in CK3.8 NWA 1559 have igneous rims and in CK4 chondrites, igneous rims are recognizable by their associated sulfide-rich rings; there are no quantifiable CV–CK differences in igneous-rim abundances. We used Ca and Al maps to show that CK chondrites have CAI abundances similar to those of CV chondrites. It thus appears that there are no resolvable pre-metamorphic petrographic differences between CV and CK chondrites. We recommend that the “CK” designation be abandoned and that the CV group be acknowledged as spanning the range of petrologic types 3–6. We suggest that CK3 chondrites be designated CV3OxK. Most CK4 chondrites are highly fragmental; collisional crushing appears to be much more common than in CV chondrites. It seems likely that CK chondrites formed from reduced CV3 materials after the latter was impacted, buried, aqueously altered and annealed.

The origin of chondrules and chondrites: Debris from low‐velocity impacts between molten planetesimals?

Abstract–We investigate the hypothesis that many chondrules are frozen droplets of spray from impact plumes launched when thin‐shelled, largely molten planetesimals collided at low speed during accretion. This scenario, here dubbed “splashing,” stems from evidence that such planetesimals, intensely heated by26Al, were abundant in the protoplanetary disk when chondrules were being formed approximately 2 Myr after calcium‐aluminum‐rich inclusions (CAIs), and that chondrites, far from sampling the earliest planetesimals, are made from material that accreted later, when26Al could no longer induce melting. We show how “splashing” is reconcilable with many features of chondrules, including their ages, chemistry, peak temperatures, abundances, sizes, cooling rates, indented shapes, “relict” grains, igneous rims, and metal blebs, and is also reconcilable with features that challenge the conventional view that chondrules are flash‐melted dust‐clumps, particularly the high concentrations of Na and FeO in chondrules, but also including chondrule diversity, large phenocrysts, macrochondrules, scarcity of dust‐clumps, and heating. We speculate that type I (FeO‐poor) chondrules come from planetesimals that accreted early in the reduced, partially condensed, hot inner nebula, and that type II (FeO‐rich) chondrules come from planetesimals that accreted in a later, or more distal, cool nebular setting where incorporation of water‐ice with high Δ17O aided oxidation during heating. We propose that multiple collisions and repeated re‐accretion of chondrules and other debris within restricted annular zones gave each chondrite group its distinctive properties, and led to so‐called “complementarity” and metal depletion in chondrites. We suggest that differentiated meteorites are numerically rare compared with chondrites because their initially plentiful molten parent bodies were mostly destroyed during chondrule formation.

Petrology, trace element abundances and oxygen isotopic compositions of a compound CAI–chondrule object from Allende

We report the petrology, trace element abundances and oxygen isotopic characteristics of a compound CAI–chondrule object, WI-025, found in the Allende CV3 chondrite. The WI-025 is an irregularly shaped inclusion consisting of three texturally and chemically distinct portions: the interior portion, the igneous rim and the intermediate zone located between these two portions. The interior portion consists of anorthite, spinel, olivine and Al-bearing low-Ca pyroxene. The major element chemistry of the interior portion corresponds to that of Al-rich chondrules and is of intermediate character between fine-grained spinel-rich CAIs and ferromagnesian chondrules. The interior portion has abundant 16O-rich spinel (Δ17O=−14.2 to −24.7) and displays a group II CAI-like REE composition. These observations indicate that the interior portion contains a CAI component formed by fractional condensation. The major and trace element chemistry of the interior portion indicate that the CAI had subsequently assimilated chondrule materials through partial melting. The maximum heating temperature of the partial melting is estimated at approximately 1400°C, similar to the maximum heating temperature of Type-B CAIs. The oxygen isotopic compositions of the olivine and low-Ca pyroxene (Δ17O=−6.3) in the interior portion indicate that the partial melting and chondrule assimilation took place under a moderately 16O-poor nebular gas. The igneous rim is texturally and chemically similar to ferromagnesian chondrules and entirely surrounds the interior portion. The oxygen isotopic compositions of the olivine and low-Ca pyroxene in the igneous rim are indistinguishable from those of the interior olivine and Al-bearing low-Ca pyroxenes. These observations indicate that a chondrule material, which was melted in the same nebular gas as the interior portion, was accreted to the interior portion. The intermediate zone represents a reaction zone accompanying the igneous rim formation. The formation history of WI-025 can be summarized by the following processes: (1) original CAI formation, (2) partial melting and chondrule assimilation, (3) igneous rim formation and (4) secondary alteration on the parent body.

Chondritic ingredients: I. Usual suspects and some oddballs in the Leoville CV3 meteorite

Abstract– Reduced CV3 chondrites are relatively pristine rocks and prime candidates for studies exploring processes that predated planet formation. We closely examined the petrographic features and trace elemental composition of different CV3 constituents in the accretionary breccia Leoville. The petrographic results are presented here. Our sample (2.2 cm2) is not brecciated. The main ingredient—about 65 area%—is fine‐ to coarse‐grained ferromagnesian type I chondrules. Minor constituents (in order of 2‐D abundance) include refractory inclusions, Al‐rich chondrules, and very fine‐crystalline clasts of moderately volatile composition. Type II chondrules and metal nuggets occur sporadically. The chondrule–matrix ratio is approximately 3:1. Medium‐ and coarse‐grained chondrules exhibit porphyritic textures, probably caused by incomplete melting, and frequent, partial or continuous, recrystallized dust rims. The fine‐grained population most likely represents randomly sectioned dust rims. The rim material and some of the medium‐grained objects are relatively troilite‐rich. Iron‐nickel metal is rare. In addition, almost all constituents show strikingly ragged or convoluted outlines. Only a few, rim‐less components exhibit smooth contours. Evidence for incomplete melting and the formation of recrystallized or igneous rims in carbonaceous chondrites is well established, suggesting that both processes were widespread events. The observed features in Leoville support this conclusion. In addition, our findings indicate that surface abrasion in a turbulent dust‐filled regime may have taken place after the consolidation of dust rims. Alternatively, the irregular, convoluted nature of at least the rimmed chondrules may have been inherent to the dust accretion event and was not erased by subsequent heating.

Physical properties of chondrules in different chondrite groups: Implications for multiple melting events in dusty environments

Chondrite groups (CV, CK, CR) with large average chondrule sizes have low proportions of RP plus C chondrules, high proportions of enveloping compound chondrules, high proportions of chondrules with (thick) igneous rims, and relatively low proportions of type-I chondrules containing sulfide. In contrast, chondrite groups (CM, CO, OC, R, EH, EL) with smaller average chondrule sizes have the opposite properties. Equilibrated CK chondrites have plagioclase with relatively low Na; equilibrated OC, R, EH and EL chondrites have more sodic plagioclase. Enveloping compound chondrules and chondrules with igneous rims formed during a remelting event after the primary chondrule was incorporated into a dustball. Repeated episodes of remelting after chondrules were surrounded by dust would tend to produce large chondrules. RP and C chondrules formed by complete melting of their precursor assemblages; remelting of RP and C chondrules surrounded by dust would tend to produce porphyritic chondrules as small dust particles mixed with the melt, providing nuclei for crystallizing phenocrysts. This process would tend to diminish the numbers of RP and C chondrules. Correlations among these chondrule physical properties suggest that chondrite groups with large chondrules were typically surrounded by thick dust-rich mantles that formed in locally dusty nebular environments. Chondrules that were surrounded by thick dust mantles tended to cool more slowly because heat could not quickly radiate away. Slow cooling led to enhanced migration of sulfide to chondrule surfaces and more extensive sulfide evaporation. These chondrules also lost Na; the plagioclase that formed from equilibrated CK chondrites was thus depleted in Na.

Quantifying the error of 2D bulk chondrule analyses using a computer model to simulate chondrules (SIMCHON)

– Bulk chondrule compositions are important to many questions in cosmochemistry, however, the number of available bulk chondrule data sets is still small. A main reason for this is the difficulties of determining bulk chondrule compositions. A commonly used technique is to obtain 2D bulk chondrule compositions from meteorite sections. This technique has an error that we quantify here for the first time using a mathematical model of a chondrule called SIMCHON. The theoretically calculated errors are compared to errors that we determined from serial sectioning of eight Efremovka chondrules. The errors obtained from both approaches are in excellent agreement, proving that our mathematical model produces reliable errors that can be assigned to 2D bulk chondrule compositions. These errors allow a much better interpretation of 2D bulk chondrule data. We provide a table that contains typical errors for 2D bulk compositions of porphyritic chondrules. The errors are in the range of ±<1–30 relative-%. This should be acceptable for many problems in cosmochemistry. The effect of a chemical layering inside chondrules and the occurrence of a rim around them, as well as the occurrence of opaque and other accessory phases have been studied. A spreadsheet is provided that enables the calculation of errors for any desired chondrule mineral composition. BO chondrules have a negligible error, but it is impossible to provide reasonable error estimates for BO chondrules with an igneous rim. Radial pyroxene chondrules have negligible errors.

Type C Ca, Al-rich inclusions from Allende: Evidence for multistage formation

The coarse-grained, igneous, anorthite-rich (Type C) CAIs from Allende studied ( 100, 160, 6-1-72, 3529-40, CG5, ABC, TS26, and 93) have diverse textures and mineralogies, suggesting complex nebular and asteroidal formation histories. CAIs 100, 160, 6-1-72, and 3529-40 consist of Al,Ti-diopside (fassaite; 13–23 wt% Al 2O 3, 2–14 wt% TiO 2), Na-bearing åkermanitic melilite (0.1–0.4 wt% Na 2O; Åk 30–75), spinel, and fine-grained (∼5–10 μm) anorthite groundmass. Most of the fassaite and melilite grains have “lacy” textures characterized by the presence of abundant rounded and prismatic inclusions of anorthite ∼5–10 μm in size. Lacy melilite is pseudomorphed to varying degrees by grossular, monticellite, and pure forsterite or wollastonite. CAI 6-1-72 contains a relict Type B CAI-like portion composed of polycrystalline gehlenitic melilite (Åk 10–40), fassaite, spinel, perovskite, and platinum-group element nuggets; the Type B-like material is overgrown by lacy melilite and fassaite. Some melilite and fassaite grains in CAIs 100 and 160 are texturally similar to those in the Type B portion of 6-1-72. CAIs ABC and TS26 contain relict chondrule fragments composed of forsteritic olivine and low-Ca pyroxene; CAI 93 is overgrown by a coarse-grained igneous rim of pigeonite, augite, and anorthitic plagioclase. These three CAIs contain very sodium-rich åkermanitic melilite (0.4–0.6 wt% Na 2O; Åk 63–74) and Cr-bearing Al,Ti-diopside (up to 1.6 wt% Cr 2O 3, 1–23 wt% Al 2O, 0.5–7 wt% TiO 2). Melilite and anorthite in the Allende Type C CAI peripheries are replaced by nepheline and sodalite, which are crosscut by andradite-bearing veins; spinel is enriched in FeO. The CAI fragment CG5 is texturally and mineralogically distinct from other Allende Type Cs. It is anorthite-poor and very rich in spinel poikilitically enclosed by Na-free gehlenitic melilite (Åk 20–30), fassaite, and anorthite; neither melilite nor pyroxene have lacy textures; secondary minerals are absent. The Al-rich chondrules 3655b-2 and 3510-7 contain aluminum-rich and ferromagnesian portions. The Al-rich portions consist of anorthitic plagioclase, Al-rich low-Ca pyroxene, and Cr-bearing spinel; the ferromagnesium portions consist of fosteritic olivine, low-Ca pyroxene, and opaque nodules. We conclude that Type C CAIs 100, 160, 6-1-72, and 3529-40 formed by melting of coarse-grained Type B-like CAIs which experienced either extensive replacement of melilite and spinel mainly by anorthite and diopside (traces of secondary Na-bearing minerals, e.g., nepheline or sodalite, might have formed as well), or addition of silica and sodium during the melting event. CG5 could have formed by melting of fine-grained spinel-melilite CAI with melilite and spinel partially replaced anorthite and diopside. CAIs ABC, 93, and TS-26 experienced melting in the chondrule-forming regions with addition of chondrule-like material, such as forsteritic olivine, low-Ca pyroxene, and high-Ca pyroxene. Anorthite-rich chondrules formed by melting of the Al-rich (Type C CAI-like) precursors mixed with ferromagnesian, Type I chondrule-like precursors. The Allende Type C CAIs and Al-rich chondrules experienced fluid-assisted thermal metamorphism, which resulted in pseudomorphic replacement of melilite and anorthite by grossular, monticellite, and forsterite ( 100, 160, 6-1-72, 3592-40) or by grossular, monticellite, and wollastonite ( ABC, 93, TS-26). The pseudomorphic replacement was followed or accompanied by iron–alkali metasomatic alteration resulting in replacement of melilite and anorthite by nepheline and sodalite, enrichment of spinel in FeO, and precipitation of salite–hedenbergite pyroxenes, wollastonite, and andradite in fractures and pores in and around CAIs.

Chondrules in the CB/CH-like carbonaceous chondrite Isheyevo: Evidence for various chondrule-forming mechanisms and multiple chondrule generations

The recently discovered metal-rich carbonaceous chondrite Isheyevo consists of Fe, Ni-metal grains, chondrules, heavily hydrated matrix lumps and rare refractory inclusions. It contains several lithologies with mineralogical characteristics intermediate between the CH and CB carbonaceous chondrites; the contacts between the lithologies are often gradual. Here we report the mineralogy and petrography of chondrules in the metal-rich (∼70 vol%) and metal-poor (∼20 vol%) lithologies. The chondrules show large variations in textures [cryptocrystalline, skeletal olivine, barred olivine, porphyritic olivine, porphyritic olivine-pyroxene, porphyritic pyroxene], mineralogy and bulk chemistry (magnesian, ferrous, aluminum-rich, silica-rich). The porphyritic magnesian (Type I) and ferrous (Type II) chondrules, as well as silica- and Al-rich plagioclase-bearing chondrules are texturally and mineralogically similar to those in other chondrite groups and probably formed by melting of mineralogically diverse precursor materials. We note, however, that in contrast to porphyritic chondrules in other chondrite groups, those in Isheyevo show little evidence for multiple melting events; e.g., relict grains are rare and igneous rims or independent compound chondrules have not been found. The magnesian cryptocrystalline and skeletal olivine chondrules are chemically and mineralogically similar to those in the CH and CB carbonaceous chondrites Hammadah al Hamra 237, Queen Alexandra Range 94411 (QUE94411) and MacAlpine Hills 02675 (MAC02675), possibly indicating a common origin from a vapor–melt plume produced by a giant impact between planetary embryos; the interchondrule metal grains, many of which are chemically zoned, probably formed during the same event. The magnesian cryptocrystalline chondrules have olivine–pyroxene normative compositions and are generally highly depleted in Ca, Al, Ti, Mn and Na; they occasionally occur inside chemically zoned Fe, Ni-metal grains. The skeletal olivine chondrules consist of skeletal forsteritic olivine grains overgrown by Al-rich (up to 20 wt% Al 2O 3) low-Ca and high-Ca pyroxene, and interstitial anorthite-rich mesostasis. Since chondrules with such characteristics are absent in ordinary, enstatite and other carbonaceous chondrite groups, the impact-related chondrule-forming mechanism could be unique for the CH and CB chondrites. We conclude that Isheyevo and probably other CH chondrites contain chondrules of several generations, which may have formed at different times, places and by different mechanisms, and subsequently accreted together with the heavily hydrated matrix lumps and refractory inclusions into a CH parent body. Short-lived isotope chronology, oxygen isotope and trace element studies of the Isheyevo chondrules can provide a possible test of this hypothesis.

Igneous rims on micrometeorites

Melting of micrometeorites (MMs) due to atmospheric entry heating causes significant changes in the textures, mineralogies and compositions of particles that obscure their primary properties and greatly complicate interpretation of these extraterrestrial materials. Despite the abundance of melted MMs, the nature of melting processes in these materials is poorly constrained. In this study, mineralogical, textural, and compositional data on 77 MMs with igneous rims are presented, which suggest that fusion of micrometeorites during atmospheric entry occurs initially by surface melting. Textural and mineralogical evidence are presented that demonstrate unequivocally that igneous rims crystallized from a melt surrounding a largely unmelted core and establish melting as a gradational process. The compositions of igneous rims on fine-grained MMs (fgMMs) are broadly similar to those of the unmelted core except for depletions in volatile and moderately volatile elements produced by partial evaporation and suggest the formation of the rims by melting of the fine-grained matrix core. Enrichments in Fe/Si, Ni/Si, and Mn/Si in igneous rims compared with unmelted cores within fgMMs are suggested to occur due to the migration of Fe–S eutectic liquids from the core of the particle into the surface melt layer. The sulphide liquids are probably generated in the core of the particle under reducing conditions resulting by the pyrolysis of carbonaceous materials. The presence of igneous rims on fgMMs is enabled by the thermal decomposition of phyllosilicates and, therefore, indicates that fgMMs were hydrated particles prior to atmospheric entry. In contrast the compositions of igneous rims on coarse-grained MMs (cgMMs) are difficult to reconcile with those of the unmelted core and instead closely resemble those of fgMMs. The igneous rims of cgMMs are, therefore, suggested to form by melting of fine-grained matrix that was present on the exterior of these particles prior to atmospheric entry. Coarse-grained MMs with igneous rims thus were originally composite micrometeoroids, which consist of both fine-grained and coarse-grained materials, and are thought to be samples of chondrule-like objects. The abundance of composite MMs to cgMMs allows a first estimate of the mean chondrule radius within the parent bodies of MMs of ∼625 μm to be made.

Origin of low-Ca pyroxene in amoeboid olivine aggregates: Evidence from oxygen isotopic compositions

Amoeboid olivine aggregates (AOAs) in primitive carbonaceous chondrites consist of forsterite (Fa <2), Fe,Ni-metal, spinel, Al-diopside, anorthite, and rare gehlenitic melilite (Åk <15). ∼10% of AOAs contain low-Ca pyroxene (Fs 1–3Wo 1–5) that is in corrosion relationship with forsterite and is found in three major textural occurrences: ( i) thin (<15 μm) discontinuous layers around forsterite grains or along forsterite grain boundaries in AOA peripheries; ( ii) 5–10-μm-thick haloes and subhedral grains around Fe,Ni-metal nodules in AOA peripheries, and ( iii) shells of variable thickness (up to 70 μm), commonly with abundant tiny (3–5 μm) inclusions of Fe,Ni-metal grains, around AOAs. AOAs with the low-Ca pyroxene shells are compact and contain euhedral grains of Al-diopside surrounded by anorthite, suggesting small (10%–20%) degree of melting. AOAs with other textural occurrences of low-Ca pyroxene are rather porous. Forsterite grains in AOAs with low-Ca pyroxene have generally 16O-rich isotopic compositions (Δ 17O < −20‰). Low-Ca pyroxenes of the textural occurrences ( i) and ( ii) are 16O-enriched (Δ 17O < −20‰), whereas those of ( iii) are 16O-depleted (Δ 17O = −6‰ to −4‰). One of the extensively melted (>50%) objects is texturally and mineralogically intermediate between AOAs and Al-rich chondrules. It consists of euhedral forsterite grains, pigeonite, augite, anorthitic mesostasis, abundant anhedral spinel grains, and minor Fe,Ni-metal; it is surrounded by a coarse-grained igneous rim largely composed of low-Ca pyroxene with abundant Fe,Ni-metal-sulfide nodules. The mineralogical observations suggest that only spinel grains in this igneous object were not melted. The spinel is 16O-rich (Δ 17O ∼ −22‰), whereas the neighboring plagioclase mesostasis is 16O-depleted (Δ 17O ∼ −11‰). We conclude that AOAs are aggregates of solar nebular condensates (forsterite, Fe,Ni-metal, and CAIs composed of Al-diopside, anorthite, spinel, and ±melilite) formed in an 16O-rich gaseous reservoir, probably CAI-forming region(s). Solid or incipiently melted forsterite in some AOAs reacted with gaseous SiO in the same nebular region to form low-Ca pyroxene. Some other AOAs appear to have accreted 16O-poor pyroxene-normative dust and experienced varying degrees of melting, most likely in chondrule-forming region(s). The most extensively melted AOAs experienced oxygen isotope exchange with 16O-poor nebular gas and may have been transformed into chondrules. The original 16O-rich signature of the precursor materials of such chondrules is preserved only in incompletely melted grains.

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 &lt;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 (&gt;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.

Amoeboid olivine aggregates with low-Ca pyroxenes: a genetic link between refractory inclusions and chondrules?

Amoeboid olivine aggregates (AOAs) in primitive (unmetamorphosed and unaltered) carbonaceous chondrites are uniformly 16O-enriched (Δ 17O ∼ −20‰) and consist of forsterite (Fa <2), FeNi-metal, and a refractory component (individual CAIs and fine-grained minerals interspersed with forsterite grains) composed of Al-diopside, anorthite, ±spinel, and exceptionally rare melilite (Åk <15); some CAIs in AOAs have compact, igneous textures. Melilite in AOAs is replaced by a fine-grained mixture of spinel, Al-diopside, and anorthite. Spinel is corroded by anorthite or by Al-diopside. In ∼10% of > 500 AOAs studied in the CR, CV, CM, CO, CH, CB, and ungrouped carbonaceous chondrites Acfer 094, Adelaide, and LEW85332, forsterite is replaced to a various degree by low-Ca pyroxene. There are three major textural occurrences of low-Ca pyroxene in AOAs: (i) thin (<10 μm) discontinuous layers around forsterite grains or along forsterite grain boundaries in AOA peripheries; (ii) haloes and subhedral grains around FeNi-metal nodules in AOA peripheries, and (iii) thick (up to 70 μm) continuous layers with abundant tiny inclusions of FeNi-metal grains around AOAs. AOAs with low-Ca pyroxene appear to have experienced melting of various degrees. In the most extensively melted AOA in the CV chondrite Leoville, only spinel grains are relict; forsterite, anorthite and Al-diopside were melted. This AOA has an igneous rim of low-Ca pyroxene with abundant FeNi-metal nodules and is texturally similar to Type I chondrules. Based on these observations and thermodynamic analysis, we conclude that AOAs are aggregates of relatively low temperature solar nebular condensates originated in 16O-rich gaseous reservoir(s), probably CAI-forming region(s). Some of the CAIs were melted before aggregation into AOAs. Many AOAs must have also experienced melting, but of a much smaller degree than chondrules. Before and possibly after aggregation, melilite and spinel reacted with the gaseous SiO and Mg to form Ca-Tschermakite (CaAl 2SiO 6)-diopside (CaMgSi 2O 6) solid solution and anorthite. Solid or incipiently melted olivine in some AOAs reacted with gaseous SiO in the CAI- or chondrule-forming regions to form low-Ca pyroxene: Mg 2SiO 4 + SiO (g) + H 2O (g) = Mg 2Si 2O 6 + H 2(g). Some low-Ca pyroxenes in AOAs may have formed by oxidation of Si-bearing FeNi-metal: Mg 2SiO 4 + Si (in FeNi) + 2H 2O (g) = Mg 2Si 2O 6 + 2H 2(g) and by direct gas-solid condensation: Mg (g) + SiO (g) +H 2O (g) = Mg 2Si 2O 6(s) + H 2(g) from fractionated (Mg/Si ratio < solar) nebular gas. Although bulk compositions of AOAs are rather similar to those of Type I chondrules, on the projection from spinel onto the plane Ca 2SiO 4-Mg 2SiO 4-Al 2O 3, these objects plot on different sides of the anorthite-forsterite thermal divide, suggesting that Type I chondrules cannot be produced from AOAs by an igneous fractionation. Formation of low-Ca pyroxene by reaction of AOAs with gaseous SiO and by melting of silica-rich dust accreted around AOAs moves bulk compositions of the AOAs towards chondrules, and provide possible mechanisms of transformation of refractory materials into chondrules or chondrule precursors. The rare occurrences of low-Ca pyroxene in AOAs may indicate that either AOAs were isolated from the hot nebular gas before condensation of low-Ca pyroxene or that condensation of low-Ca pyroxene by reaction between forsterite and gaseous SiO was kinetically inhibited. If the latter is correct, then the common occurrences of pyroxene-rich Type I chondrules may require either direct condensation of low-Ca pyroxenes or SiO 2 from fractionated nebular gas or condensation of gaseous SiO into chondrule melts.

Plagioclase‐rich chondrules in the reduced CV chondrites: Evidence for complex formation history and genetic links between calcium‐aluminum‐rich inclusions and ferromagnesian chondrules

Abstract— Plagioclase‐rich chondrules (PRCs) in the reduced CV chondrites Efremovka, Leoville, Vigarano and Grosvenor Mountains (GRO) 94329 consist of magnesian low‐Ca pyroxene, Al‐Ti‐Cr‐rich pigeonite and augite, forsterite, anorthitic plagioclase, FeNi‐metal‐sulfide nodules, and crystalline mesostasis composed of silica, anorthitic plagioclase and Al‐Ti‐Cr‐rich augite. The silica grains in the mesostases of the CV PRCs are typically replaced by hedenbergitic pyroxenes, whereas anorthitic plagioclase is replaced by feldspathoids (nepheline and minor sodalite). Some of the PRCs contain regions that are texturally and mineralogically similar to type I chondrules and consist of forsterite, low‐Ca pyroxene and abundant FeNi‐metal nodules. Several PRCs are surrounded by igneous rims or form independent compound objects. Twelve PRCs contain relic calcium‐aluminum‐rich inclusions (CAIs) composed of anorthite, spinel, high‐Ca pyroxene, ± forsterite, and ± Al‐rich low‐Ca pyroxene. Anorthite of these CAIs is generally more heavily replaced by feldspathoids than anorthitic plagioclase of the host chondrules. This suggests that either the alteration predated formation of the PRCs or that anorthite of the relic CAIs was more susceptible to the alteration than anorthitic plagioclase of the host chondrules. These observations and the presence of igneous rims around PRCs and independent compound PRCs suggest that the CV PRCs may have had a complex, multistage formation history compared to a more simple formation history of the CR PRCs.Relatively high abundances of moderately‐volatile elements such as Cr, Mn and Si in the PRCs suggests that these chondrules could not have been produced by volatilization of ferromagnesian chondrule precursors or by melting of refractory materials only. We infer instead that PRCs in carbonaceous chondrites formed by melting of the reduced chondrule precursors (magnesian olivine and pyroxene, FeNi‐metal) mixed with refractory materials (relic CAIs) composed of anorthite, spinel, high‐Ca pyroxene, and forsterite. The mineralogical, chemical and textural similarities of the PRCs in several carbonaceous chondrite groups (CV, CO, CH, CR) and common presence of relic CAIs in these chondrules suggest that PRCs may have formed in the region(s) intermediate between the regions where CAIs and ferromagnesian chondrules originated.