Ferromagnesian Chondrules Research Articles

Deciphering recycling processes during solar system evolution from magnesium-rich relict olivine grains in type II chondrules

Ferromagnesian chondrules present a remarkable dichotomy between reduced (type I) and oxidized (type II) varieties. How these formed, and how they may be related remains contentious. Many type II chondrules, especially in carbonaceous chondrites, contain forsteritic grains in disequilibrium with FeO-rich host olivine grains, which must be relicts of precursor material. In this study, we analyzed the oxygen isotopic composition of magnesian relict and host olivine grains in type II chondrules in CO and CR chondrites. The analyzed Mg-rich relicts are generally more 16O-rich than ferroan olivine (mostly host) grains and plot in the range (in term of chemistry and isotopic composition) of type I chondrules in carbonaceous chondrites. Remarkably, they tend to cluster around the dominant Δ17O peaks of the type I chondrules in their host chondrites, viz. –6 ‰ and –2 ‰ for CO and CR, respectively. With the occurrence of relatively intact type I chondrules within some type II chondrules, this corroborates that local type I chondrules were among the precursors of type II chondrules, and that chondrule formation occurred within the accretion reservoir of the eventual chondrites. This supports the nebular brand of chondrule-forming scenarios. Since not all previous generations of chondrules (or other precursor objects) have been recycled, chondrule formation events must also have been extremely localized.

Origin of Al-rich chondrules in CV chondrites: Incorporation of diverse refractory components into the ferromagnesian chondrule-forming region

Aluminum-rich (Al2O3 > 10 wt%) chondrules (ARCs) are important chondritic components that petrologically link two other major chondritic components, ferromagnesian chondrules (FMCs) and calcium-aluminum-rich inclusions (CAIs), which formed in different regions of the protoplanetary disk. They are closely related to FMCs as indicated by their similar igneous textures, mineral assemblages, and Al-Mg isotope systematics; meanwhile, they have genetic a relationship with CAIs as indicated by their distinctly Al2O3-rich compositions and occasional occurrences of relict CAI minerals. In order to further understand their formation mechanism and genetic relationships to FMCs and CAIs, nine ARCs and three ARC-related objects from Allende (CV3 oxidized), Leoville (CV3 reduced), and the ungrouped Ningqiang carbonaceous chondrites were studied for petrology, mineralogy, bulk compositions, rare earth element (REE) abundances, and in situ oxygen isotopic compositions. Our results suggest that (i) ARCs crystallized from incompletely molten droplets with crystallization sequences mainly determined based on their bulk compositions. Projection of their bulk compositions onto the forsterite-saturated tridymite-diopside-spinel diagram allows us to classify them into Al-rich [Sp], Al-rich [En], and Al-rich [Plag]; (ii) ARC precursors are mixtures of refractory materials and the precursors of FMCs, in which the refractory materials have diverse sources rather than a single type of CAI/AOA (amoeboid olivine aggregate); this is inferred from the bulk compositions, relict minerals (both coarse- and fine-grained spinel, olivine, and Al-Ti-diopside), and various CAI-like REE patterns (unfractionated Group I/III and highly fractionated Group II/II-like) of ARCs. The sources include AOAs and igneous Type B/C CAIs; (iii) ARCs were melted in the FMC-forming region, possibly by the same heating mechanism or during the same transient heating event, which is consistent with the similar oxygen isotopic compositions of their phenocrysts (Δ17O = −5.2 ± 1.7‰, 2SD). Thus, we consider that ARCs formed by melting of mixtures of diverse refractory components with the FMC precursors in the FMC-forming region.

Time and duration of chondrule formation: Constraints from 26Al-26Mg ages of individual chondrules

Chondrules from unequilibrated ordinary and carbonaceous chondrites belong to the oldest and most primitive materials from the early solar system and record chemical and isotopic signatures relating to their formation and evolution. These signatures allow tracing protoplanetary disk processes that eventually led to the formation of planetary building blocks and rocky planets. 26Al-26Mg ages based on mineral-mesostasis isochrons of 31 porphyritic ferromagnesian chondrules, that belong mainly to type-II, constrain the time of chondrule melting prior to incorporation into the respective chondrite parent bodies. For this study chondrules from the unequilibrated L, L(LL) and LL ordinary chondrites (UOCs) NWA 5206, NWA 8276, MET 96503, MET 00452, MET 00526, NWA 7936 and QUE 97008 were selected, which are of petrologic types 3.00–3.15 and were thus least metamorphosed after formation. Magnesium and Al isotopes were measured in-situ by Secondary Ion Mass Spectrometry (SIMS) using a CAMECA 1280 ims. 26Mg excess from in-situ decay of 26Al correlating with 27Al/24Mg has been detected in the mesostasis of all but one chondrule. The initial Al isotopic compositions (26Al/27Al)0 and 26Mg/24Mg ratios (δ26Mg0∗) deduced from internal mineral isochron regressions range from (9.5 ± 2.8) × 10−6 to (3.1 ± 1.2) × 10−6 and −0.020 ± 0.028‰ to 0.011 ± 0.039‰, respectively. The corresponding chondrule ages (ΔtCAI), calculated relative to calcium-aluminum-rich inclusions (CAIs) using the canonical 26Al/27Al = (5.23 ± 0.13) × 10−5, are between 1.76-0.27+0.36 and 2.92-0.34+0.51 Ma and date the melt formation and thus primary chondrule formation from dust-like precursors or reprocessing of older chondrules. The age range agrees with those acquired with different short-lived chronometers and with published 26Al-26Mg ages, the majority of which were obtained for chondrules from the Bishunpur and Semarkona meteorites, although no chondrule with (26Al/27Al)0 > 10−5 was found.Chondrules in single chondrite samples or between different chondrite groups show no distinct age distributions. The initial 26Al/27Al of the oldest chondrules in the L(LL)/LL and L chondrite samples are identical within their 1σ uncertainties and yield a mean age of 1.99-0.08+0.08 Ma and 1.81-0.10+0.11 Ma, respectively. The oldest chondrules from six of the seven studied samples record a mean age of 1.94-0.06+0.07 Ma. Since heating events in the protoplanetary disk could have partially reset the Al-Mg systematics in pre-existing chondrules and this would have shifted recorded 26Al-26Mg ages toward younger dates, the oldest mean age of 1.81-0.10+0.11 Ma recorded in L chondrite chondrules is interpreted to date the rapid and punctuated onset of chondrule formation. The density distribution of chondrule ages from this study, which comprises the largest single dataset of OC chondrule ages, combined with published ages for chondrules from ordinary and carbonaceous chondrites reveals major age peaks for OC chondrules at 2.0 and 2.3 Ma. Chondrules in ordinary and carbonaceous chondrites formed almost contemporaneously (with a possible distinction between CC groups) in two chemically distinct reservoirs, probably in density-enriched regions at the edges of Jupiter’s orbit. The young formation ages of chondrules suggest that they do not represent precursors but rather by-products of planetesimal accretion.

Chronology of formation of early solar system solids from bulk Mg isotope analyses of CV3 chondrules

We have analysed the petrography, major element abundances and bulk Al-Mg isotope systematics of 19 ferromagnesian chondrules from the CV3 chondrites Allende, Mokoia, and Vigarano, together with an Al-rich chondrule and refractory olivine from Mokoia. Co-variations of Al/Mg with Na/Mg and Ti/Mg in our bulk chondrules suggest their compositions are dominantly controlled by reworking of different proportions of chondrule components (e.g. mafic minerals and mesostatis); their precursors are thus fragments from prior generations of chondrules. Our samples show a range in fractionation corrected 26Mg/24Mg (Δ′26Mg) ∼ 60 ppm, relative to precisions <±5 ppm (2se) and these values broadly covary with 27Al/24Mg. The data can be used to calculate model initial 26Al/27Al, or (26Al/27Al)0, of the chondrule precursors. Our resolvably radiogenic chondrules yield model (26Al/27Al)0 ∼ 1–2 × 10−5, equivalent to model “ages” of precursor formation ≦1 Ma post CAI. However, many of our chondrules show near solar Δ′26Mg and no variability despite a range in 27Al/24Mg. This suggests their derivation either from younger precursor chondrules or open system behaviour once 26Al was effectively extinct ((26Al/27Al)0 < 0.8 × 10−5, given the resolution here). Evidence for the latter explanation is provided by marked rims of orthopyroxene replacing olivine, indicating reaction of chondrules with a surrounding silicate vapour. Concurrent isotopic exchange of Mg with a near chondritic vapour during late reworking could explain their isotopic systematics. One ferromagnesian object is dominated by a high Mg# olivine with elevated Ti and Ca abundances. This refractory olivine has a markedly negative Δ′26Mg = −16 ± 3 ppm (2se), reflecting its early removal (model age of <0.5 Ma post CAI), from a reservoir with evolving Δ′26Mg. If representative of the chondrule forming region, this grain defines a minimum interval of radiogenic ingrowth for CV chondrites commensurate with (26Al/27Al)0 > 3.4 ± 0.6 × 10−5. Overall, our samples record a sequence of events from the formation of ferromagnesian objects within 0.5 Ma of CAI to re-equilibration of chondrules and silicate vapour >2 Ma post CAI, assuming an initially homogeneous 26Al/27Al. Metamorphism on the asteroid parent body may have played a subsequent role in affecting Mg isotope composition, but we argue this had a minor influence on the observations here.

Relationship between CAIs and chondrules: A case study of a compound chondrule from the Allende (CV3) meteorite

We report the mineralogy, petrology, major, minor and trace element geochemistry, O and Si isotopes of a complex compound chondrule from the Allende meteorite. The chondrule contains zones of refractory (Ca, Al-rich) regions along with regions more similar to ferromagnesian chondrules. The bulk silicon isotopic composition of the object is δ30Si = –0.71 ± 0.03‰. The oxygen isotopic composition of the different phases within the compound chondrules fall along the Allende chondrule line and range from Δ17O – 12.5 to –2‰. Rare earth element abundances are enriched compared to chondritic levels by up to 15× CI, and show a nebular condensate signature with depletions in Eu and Yb. Our data show that the object evolved in oxygen isotopes in a nebular environment, most likely due to formation from a mixture of diverse components combined with interaction with nebular gas. In addition, differences in olivine composition across the inclusion suggest isotopically distinct oxygen regions also existed in dust in the protoplanetary disk. This object and other compound objects demonstrate that CAIs were present in the chondrule forming region, however they are not found in the majority of chondrules. We speculate that the bulk of the CAIs may have been added into the CV parent body after initial accretion of the body.

Petrology, mineralogy, and oxygen isotope compositions of aluminum-rich chondrules from CV3 chondrites

Bulk major element composition, petrography, mineralogy, and oxygen isotope compositions of twenty Al-rich chondrules (ARCs) from five CV3 chondrites (Northwest Africa [NWA] 989, NWA 2086, NWA 2140, NWA 2697, NWA 3118) and the Ningqiang carbonaceous chondrite were studied and compared with those of ferromagnesian chondrules and refractory inclusions. Most ARCs are marginally Al-richer than ferromagnesian chondrules with bulk Al2O3 of 10–15 wt%. ARCs are texturally similar to ferromagnesian chondrules, composed primarily of olivine, pyroxene, plagioclase, spinel, Al-rich glass, and metallic phases. Minerals in ARCs have intermediate compositions. Low-Ca pyroxene (Fs0.6–8.8Wo0.7–9.3) has much higher Al2O3 and TiO2 contents (up to 12.5 and 2.3 wt%, respectively) than that in ferromagnesian chondrules. High-Ca pyroxene (Fs0.3–2.0Wo33–54) contains less Al2O3 and TiO2 than that in Ca,Al-rich inclusions (CAIs). Plagioclase (An77–99Ab1–23) is much more sodic than that in CAIs. Spinel is enriched in moderately volatile element Cr (up to 6.7 wt%) compared to that in CAIs. Al-rich enstatite coexists with anorthite and spinel in a glass-free chondrule, implying that the formation of Al-enstatite was not due to kinetic reasons but is likely due to the high Al2O3/CaO ratio (7.4) of the bulk chondrule. Three ARCs contain relict CAIs. Oxygen isotope compositions of ARCs are also intermediate between those of ferromagnesian chondrules and CAIs. They vary from −39.4‰ to 13.9‰ in δ18O and yield a best fit line (slope = 0.88) close to the carbonaceous chondrite anhydrous mineral (CCAM) line. Chondrules with 5–10 wt% bulk Al2O3 have a slightly more narrow range in δ18O (−32.5 to 5.9‰) along the CCAM line. Except for the ARCs with relict phases, however, most ARCs have oxygen isotope compositions (>−20‰ in δ18O) similar to those of typical ferromagnesian chondrules. ARCs are genetically related to both ferromagnesian chondrules and CAIs, but the relationship between ARCs and ferromagnesian chondrules is closer. Most ARCs were formed during flash heating and rapid cooling processes like normal chondrules, only from chemically evolved precursors. ARCs extremely enriched in Al and those with relict phases could have had a hybrid origin (Krot et al. 2002) which incorporated refractory inclusions as part of the precursors in addition to ferromagnesian materials. The occurrence of melilite in ARCs indicates that melilite-rich CAIs might be present in the precursor materials of ARCs. The absence of melilite in most ARCs is possibly due to high-temperature interactions between a chondrule melt and the solar nebula.

In situ SIMS oxygen isotope analyses: Evidence for the formation of aluminum-rich chondrules from ordinary chondrites

Aluminum-rich chondrules (ARCs), which share mineralogic and chemical properties with both Ca, Al-rich inclusions (CAIs) and ferromagnesian chondrules, play an important role in revealing their temporal and petrogenetic relationships. In this work, seven ARCs were found in three ordinary chondrites GRV 022410 (H4), GRV 052722 (H3.7) and Julesburg (L3.6). They contain bulk Al2O3 ∼ 17%–33% and exhibit igneous textures composed of olivine, high- and low-Ca pyroxene, plagioclase, spinel and glass. In situ SIMS analyses show that ARCs have oxygen isotopic compositions (δ 18O=−6.1‰–7.1‰; δ 17O= −4.5‰–5.1‰) close to ferromagnesian chondrules but far more depleted in 16O than CAIs (δ 18O=−40‰; δ 17O=−40‰). Most ARCs plot close to the terrestrial mass fractionation (TF) line, and a few between the TF and carbonaceous chondrite anhydrous mixing (CCAM) lines. Plagioclase, nepheline and glass suffered O-isotopic exchanges during the metamorphism processes in the parent body. Spinel, olivine and pyroxene represent the primary O-isotopic compositions of ARCs, and define a fitted line with a slope of ∼ 0.7±0.1. Compared with the results of previous studies, shallower slope as well as more depleted 16O compositions further demonstrates that ARCs in ordinary chondrites are not a simple mixing product of ferromagnesian chondrules and CAIs. Instead, they probably experienced higher-degree oxygen isotope exchange with a 16O-poor nebular gas reservoir during multiple melting episodes.

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

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

EH3 matrix mineralogy with major and trace element composition compared to chondrules

AbstractWe investigated the matrix mineralogy in primitive EH3 chondrites Sahara 97072, ALH 84170, and LAR 06252 with transmission electron microscopy; measured the trace and major element compositions of Sahara 97072 matrix and ferromagnesian chondrules with laser‐ablation, inductively coupled, plasma mass spectrometry (LA‐ICPMS); and analyzed the bulk composition of Sahara 97072 with LA‐ICPMS, solution ICPMS, and inductively coupled plasma atomic emission spectroscopy. The fine‐grained matrix of EH3 chondrites is unlike that in other chondrite groups, consisting primarily of enstatite, cristobalite, troilite, and kamacite with a notable absence of olivine. Matrix and pyroxene‐rich chondrule compositions differ from one another and are distinct from the bulk meteorite. Refractory lithophile elements are enriched by a factor of 1.5–3 in chondrules relative to matrix, whereas the matrix is enriched in moderately volatile elements. The compositional relation between the chondrules and matrix is reminiscent of the difference between EH3 pyroxene‐rich chondrules and EH3 Si‐rich, highly sulfidized chondrules. Similar refractory element ratios between the matrix and the pyroxene‐rich chondrules suggest the fine‐grained material primarily consists of the shattered, sulfidized remains of the formerly pyroxene‐rich chondrules with the minor addition of metal clasts. The matrix, chondrule, and metal‐sulfide nodule compositions are probably complementary, suggesting all the components of the EH3 chondrites came from the same nebular reservoir.

Terminal particle from Stardust track 130: Probable Al-rich chondrule fragment from comet Wild 2

A 4×6μm terminal particle from Stardust track 130, named Bidi, is composed of a refractory assemblage of Fo97 olivine, Al- and Ti-bearing clinopyroxene and anorthite feldspar (An97). Mineralogically, Bidi resembles a number of components found in primitive chondritic meteorites including Al-rich chondrules, plagioclase-bearing type I ferromagnesian chondrules and amoeboid olivine aggregates (AOAs). Measured widths of augite/pigeonite lamellae in the clinopyroxene indicate fast cooling rates suggesting that Bidi is more likely to be a chondrule fragment than an AOA. Bulk element concentrations, including an Al2O3 content of 10.2wt%, further suggests that Bidi is more akin to Al-rich rather than ferromagnesian chondrules. This is supported by high anorthite content of the plagioclase feldspar, overall bulk composition and petrogenetic analysis using a cosmochemical Al2O3–Ca2SiO4–Mg2SiO4 phase diagram. Measured minor element abundances of individual minerals in Bidi generally support an Al-rich chondrule origin but are not definitive between any of the object types. Oxygen isotope ratios obtained from olivine (+minor high-Ca pyroxene)fall between the TF and CCAM lines and overlap similar minerals from chondrules in primitive chondrites but are generally distinct from pristine AOA minerals. Oxygen isotope ratios are similar to some minerals from both Al-rich and type I ferromagnesian chondrules in unequilibrated carbonaceous, enstatite and ordinary chondrites. Although no single piece of evidence uniquely identifies Bidi as a particular object type, the preponderance of data, including mineral assemblage, bulk composition, mineral chemistry, inferred cooling rates and oxygen isotope ratios, suggest that Bidi is more closely matched to Al-rich chondrules than AOAs or plagioclase-bearing type I ferromagnesian chondrules and likely originated in a chondrule-forming region in the inner solar system.

Experimental investigation of condensation predictions for dust-enriched systems

Condensation models describe the equilibrium distribution of elements between coexisting phases (mineral solid solutions, silicate liquid, and vapor) in a closed chemical system, where the vapor phase is always present, using equations of state of the phases involved at a fixed total pressure (<1bar) and temperature (T). The VAPORS code uses a CaO–MgO–Al2O3–SiO2 (CMAS) liquid model at T above the stability field of olivine, and the MELTS thermodynamics algorithm at lower T. Quenched high-T crystal+liquid assemblages are preserved in meteorites as Type B Ca-, Al-rich inclusions (CAIs), and olivine-rich ferromagnesian chondrules. Experimental tests of compositional regions within 100K of the predicted T of olivine stability may clarify the nature of the phases present, the phase boundaries, and the partition of trace elements among these phases. Twenty-three Pt-loop equilibrium experiments in seven phase fields on twelve bulk compositions at specific T and dust enrichment factors tested the predicted stability fields of forsteritic olivine (Mg2SiO4), enstatite (MgSiO3), Cr-bearing spinel (MgAl2O4), perovskite (CaTiO3), melilite (Ca2Al2SiO7–Ca2Mg2Si2O7) and/or grossite (CaAl4O7) crystallizing from liquid. Experimental results for forsterite, enstatite, and grossite are in very good agreement with predictions, both in chemistry and phase abundances. On the other hand the stability of spinel with olivine, and stability of perovskite and gehlenite are quite different from predictions. Perovskite is absent in all experiments. Even at low oxygen fugacity (IW-3.4), the most TiO2-rich experiments do not crystallize Al-, Ti-bearing calcic pyroxene. The stability of spinel and olivine together is limited to a smaller phase field than is predicted. The melilite stability field is much larger than predicted, indicating a deficiency of current liquid or melilite activity models. In that respect, these experiments contribute to improving the data for calibrating thermodynamic models including MELTS.

Origins of Al-rich chondrules: Clues from a compound Al-rich chondrule in the Dar al Gani 978 carbonaceous chondrite

Aluminum-rich chondrules are one of the most interesting components of primitive chondrites, because they have characteristics that are similar to both Ca, Al-rich inclusions (CAIs) and ferromagnesian chondrules. However, their precursor and formation history remain poorly constrained, especially with respect to their oxygen isotopic distributions. In this study, we report on the petrography, mineralogy, oxygen isotope ratios, and rare-earth-element compositions of a sapphirine-bearing Al-rich chondrule (SARC) in the ungrouped chondrite Dar al Gani (DaG) 978. The SARC has a complex core-mantle-rim texture; while both the core and the mantle are mainly composed of Al-rich enstatite and anorthite with minor amounts of mesostasis, these regions are distinguished by the presence of Fe-rich spinel and sapphirine in the core and their absence in the mantle. The rim of the SARC consists mainly of Fe-rich olivine, enstatite, and Fe–Ni metal. Spinel and some olivine grains in the SARC are 16O-rich, with Δ17O values down to −20‰ and −23‰, respectively. Enstatite, sapphirine, and most olivine grains have similar Δ17O values (∼ −7‰), which are lower than those of anorthite and the mesostasis (including augite therein) (Δ17O: ∼ −3‰). Mesostasis from both the core and mantle have Group II rare-earth-element (REE) patterns; however, the core mesostasis has higher REE concentrations than the mantle mesostasis. These observations provide a strong indication that the SARC formed by the melting and crystallization of a mixture of materials from Group II CAIs and ferromagnesian chondrules. Both spinel and olivine with 16O-rich features could be of relict origin. The 16O-poor isotopic compositions of most components in Al-rich chondrules can be explained by oxygen isotopic exchange between the melt and 16O-poor nebular gas (Δ17O: ∼ −7‰) during melting in chondrule-forming regions; whereas the anorthite and mesostasis could have experienced further oxygen isotopic exchange with a relatively 16O-poor reservoir (Δ17O: ∼ −3‰) on the parent body, likely during fluid-assisted thermal metamorphism. During the same thermal metamorphism event, spinel, olivine, some enstatite, and the mesostasis experienced Mg–Fe exchange to various extents.

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.

The formation and alteration of the Renazzo-like carbonaceous chondrites II: Linking O-isotope composition and oxidation state of chondrule olivine

To better understand the formation conditions of type-I and type-II chondrules in the Renazzo-like carbonaceous (CR) chondrites, an in situ major- and minor-element and O-isotope study was conducted. Twenty-one ferromagnesian chondrules from three CR chondrites (GRA 95229, GRA 06100, and QUE 99177) were analyzed to establish an internally-consistent data set. From this study we infer that type-II chondrule precursors contained enhanced S-bearing dust and ice abundances relative to type-I chondrules. There is a relationship between the O-isotope composition and oxidation state of olivine, which may be related to the amount of 16O-poor ice and reduced carbon accreted by chondrule precursors before melting. Type-II chondrules formed under H2O/H2 ratios of ∼230–740 times solar. In contrast, type-I chondrules formed under more reducing conditions with lower H2O/H2 ratios of ∼10–100 times solar. We find a relationship between type-II chondrule petrology (relict free vs. relict grain-bearing) and O-isotope composition, which is due to degree of melting and exchange with a 16O-poor gas reservoir. The 16O-poor gas that interacted with both type-I and type-II chondrules is estimated to have an isotopic composition between ∼δ18Og=13–27‰ and δ17Og=10–22‰, different from the O-isotope composition of the water accreted by the CR chondrite parent body. Due to partial melting, type-I chondrules and relict grain-bearing type-II chondrules exchanged with the 16O-poor gas to a lower degree than relict-free type-II chondrules.

Lack of relationship between 26Al ages of chondrules and their mineralogical and chemical compositions

Previous studies have suggested the existence of a correlation between 26Al relative crystallisation ages and mineralogical and bulk chemical compositions of ferromagnesian chondrules from the Bishunpur and Semarkona unequilibrated ordinary (Mostefaoui et al., 2002; Tachibana et al., 2003). However, because the precision in 26Al ages was moderate, these correlations are questionable. Here, we report mineralogical and chemical compositions of 14 ferromagnesian chondrules from Semarkona for which precise 26Al ages were previously obtained (Villeneuve et al., 2009). We find global correlation of 26Al ages neither with bulk chemical composition of chondrules, nor with the different types of ferromagnesian chondrules, i.e. PO, POP and PP. This indicates that if some kind of correlations between chemical compositions of chondrules and their ages of formation exists, they do not exist at timescales that can be measured with the 26Al-26Mg systematics but presumably at much shorter timescales.

Equilibrium condensation from chondritic porous IDP enriched vapor: Implications for Mercury and enstatite chondrite origins

The origin of Mercury's anomalous core and low FeO surface mineralogy are outstanding questions in planetary science. Mercury's composition may result from cosmochemical controls on the precursor solids that accreted to form Mercury. High temperatures and enrichment in solid condensates are likely conditions near the midplane of the inner solar protoplanetary disk. Silicate liquids similar to the liquids quenched in ferromagnesian chondrules are thermodynamically stable in oxygen-rich systems that are highly enriched in dust of CI-chondrite composition. In contrast, the solids surviving into the orbit of Mercury's accretion zone were probably similar to highly unequilibrated, anhydrous, interstellar organic- and presolar grain-bearing chondritic, porous interplanetary dust particles (C-IDPs). Chemical systems enriched in an assumed C-IDP composition dust produce condensates (solid+liquid assemblages in equilibrium with vapor) with super-chondritic atomic Fe/Si ratios at high temperatures, approaching 50% of that estimated for bulk Mercury. Sulfur behaves as a refractory element, but at lower temperatures, in these chemical systems. Stable minerals are FeO-poor, and include CaS and MgS, species found in enstatite chondrites. Disk gradients in volatile compositions of planetary and asteroidal precursors can explain Mercury's anomalous composition, as well as enstatite chondrite and aubrite parent body compositions. This model predicts high sulfur content, and very low FeO content of Mercury's surface rocks.

Bulk chemical compositions of Al-rich objects from Rumuruti (R) chondrites: Implications for their origin

R chondrites are a distinct group of chondritic meteorites with unique mineralogical and chemical compositions. They contain various types of Al-rich objects [Ca,Al-rich inclusions (CAIs), Al-rich chondrules and fragments], whose mineralogical compositions and classifications were previously determined by Rout and Bischoff (2008). Here, we report on the bulk compositions of 126 such Al-rich objects determined by broad-beam electron probe microanalysis. Most of the CAIs, except a few, are significantly altered by complex nebular and/or parent body processes and the determination of their pristine composition is difficult. We found that the simple concentric spinel-rich inclusions have high Al 2O 3 (21–72 wt%) correlated with their high modal spinel. The subgroup of simple concentric spinel-rich CAIs have a high Al 2O 3 (21–57 wt%) and also sometimes high FeO (up to 36 wt%), due to a high hercynitic component in the spinel. One simple concentric spinel- and hibonite-rich CAI H030/L, identified as a HAL-type CAI by isotopic studies reported elsewhere, has a highly refractory composition (Al 2O 3∼72 wt%). Most of the simple concentric spinel- and fassaite-rich CAIs have consistently high CaO (∼2.5–17 wt%) compared to other simple concentric spinel-rich inclusions group, where only some inclusions have high CaO (up to 15 wt%). Simple concentric spinel- and Na,Al-alteration product-rich CAIs are heavily altered and have high Na 2O (up to ∼12.5 wt%). The three analyzed fassaite-rich spherules have high CaO and Al 2O 3, and complex spinel- and fassaite-rich CAIs have high CaO (up to 23 wt%) and SiO 2 (up to 41 wt%). Most of the complex spinel- and plagioclase-rich CAIs are altered and contain high amounts of secondary oligoclase. However, a few are less affected by secondary alteration and these are characterized by relatively high CaO (up to 24 wt%) and Al 2O 3 (18–33 wt%); complex spinel and Na,Al-alteration product-rich CAIs are similar to the concentric spinel- and Na,Al-alteration product-rich CAIs. Due to Fe- and alkali-metasomatism, the vast majority of the inclusions in this subgroup were heavily altered, either in a nebular or parent body environment. As a result of this alteration, they contain high FeO and Na 2O+K 2O+Cl. Almost all inclusions have a Ca/Al-ratio below the solar ratio. This suggests that significant Ca/Al fractionation occurred during the formation of most CAIs, most probably due to disequilibrium condensation of spinel prior to melilite. However, a distillation process cannot be ruled out for some CAIs in producing the spinel enrichment. Some porous and fine grained CAIs may have been produced by agglomeration of refractory dust rich in spinel and fassaite. The HAL-type CAI, H030/L, most likely formed by distillation, similar to most of the HAL-type inclusions. Phase equilibrium analysis, in the CMAS system, shows that the fassaite-bearing spherules most likely formed by metastable crystallization and disequilibrium processes. Al-rich chondrules are characterized by >10 wt% Al 2O 3, and most of these also have high FeO and Na 2O. Considering their bulk compositions, their precursors seem to have been a mixture of a ferromagnesian chondrule component rich in olivine and an anorthite–spinel–pyroxene–nepheline-rich CAI component. The mineral assemblages of some of the less altered Al-rich chondrules conform to those predicted by phase equilibrium studies.

Refractory inclusions and aluminum‐rich chondrules in Sayh al Uhaymir 290 CH chondrite: Petrography and mineralogy

Abstract— Here we report the petrography, mineralogy, and bulk compositions of Ca,Al‐rich inclusions (CAIs), amoeboid olivine aggregate (AOA), and Al‐rich chondrules (ARCs) in Sayh al Uhaymir (SaU) 290 CH chondrite. Eighty‐two CAIs (0.1% of the section surface area) were found. They are hibonite‐rich (9%), grossite‐rich (18%), melilite ± spinel‐rich (48%), fassaite ± spinel‐rich (15%), and fassaite‐anorthite‐rich (10%) refractory inclusions. Most CAIs are rounded in shape and small in size (average = 40 μm). They are more refractory than those of other groups of chondrites. CAIs in SaU 290 might have experienced higher peak heating temperatures, which could be due to the formation region closer to the center of protoplanetary disk or have formed earlier than those of other groups of chondrites. In SaU 290, refractory inclusions with a layered texture could have formed by gas‐solid condensation from the solar nebula and those with an igneous texture could have crystallized from melt droplets or experienced subsequent melting of pre‐existing condensates from the solar nebula. One refractory inclusion represents an evaporation product of pre‐existing refractory solid on the basis of its layered texture and melting temperature of constituting minerals. Only one AOA is observed (75 μm across). It consists of olivine, Al‐diopside, anorthite, and minor spinel with a layered texture. CAIs and AOA show no significant low‐temperature aqueous alteration. ARCs in SaU 290 consist of diopside, forsterite, anorthite, Al‐enstatite, spinel, and mesostasis or glass. They can be divided into diopside‐rich, Al‐enstatite‐rich, glass‐rich, and anorthite‐rich chondrules. Bulk compositions of most ARCs are consistent with a mixture origin of CAIs and ferromagnesian chondrules. Anorthite and Al‐enstatite do not coexist in a given ARC, implying a kinetic effect on their formation.

Petrology and mineralogy of the Ningqiang carbonaceous chondrite

Abstract— We report detailed chemical, petrological, and mineralogical studies on the Ningqiang carbonaceous chondrite. Ningqiang is a unique ungrouped type 3 carbonaceous chondrite. Its bulk composition is similar to that of CV and CK chondrites, but refractory lithophile elements (1.01 × CI) are distinctly depleted relative to CV (1.29 × CI) and CK (1.20 × CI) chondrites. Ningqiang consists of 47.5 vol% chondrules, 2.0 vol% Ca,Al‐rich inclusions (CAIs), 4.5 vol% amoeboid olivine aggregates (AOAs), and 46.0 vol% matrix. Most chondrules (95%) in Ningqiang are Mg‐rich. The abundances of Fe‐rich and Al‐rich chondrules are very low. Al‐rich chondrules (ARCs) in Ningqiang are composed mainly of olivine, plagioclase, spinel, and pyroxenes. In ARCs, spinel and plagioclase are enriched in moderately volatile elements (Cr, Mn, and Na), and low‐Ca pyroxenes are enriched in refractory elements (Al and Ti). The petrology and mineralogy of ARCs in Ningqiang indicate that they were formed from hybrid precursors of ferromagnesian chondrules mixed with refractory materials during chondrule formation processes. We found 294 CAIs (55.0% type A, 39.5% spinel‐pyroxene‐rich, 4.4% hibonite‐rich, and several type C and anorthite‐spinel‐rich inclusions) and 73 AOAs in 15 Ningqiang sections (equivalent to 20 cm2surface area). This is the first report of hibonite‐rich inclusions in Ningqiang. They are texturally similar to those in CM, CH, and CB chondrites, and exhibit three textural forms: aggregates of euhedral hibonite single crystals, fine‐grained aggregates of subhedral hibonite with minor spinel, and hibonite ± Al,Ti‐diopside ± spinel spherules. Evidence of secondary alteration is ubiquitous in Ningqiang. Opaque assemblages, formed by secondary alteration of pre‐existing alloys on the parent body, are widespread in chondrules and matrix. On the other hand, nepheline and sodalite, existing in all chondritic components, formed by alkali‐halogen metasomatism in the solar nebula.

26Al– 26Mg systematics of chondrules in a primitive CO chondrite

We have conducted systematic investigations of formation age, chemical compositions, and mineralogical characteristics of ferromagnesian chondrules in Yamato-81020 (CO3.05), one of the most primitive carbonaceous chondrites, to get better understanding of the origin of chemical groups of chondrites. The 26Al– 26Mg isotopic system were measured in fourteen FeO-poor (Type I), six FeO-rich (Type II) and two aluminum-rich (Al-rich) chondrules using a secondary ion mass spectrometer. Excesses of 26Mg in plagioclase (1.0–13.5‰) are resolved with sufficient precision (mostly 0.4–6.6‰ at 2 σ level) in all the chondrules studied except one. Chemical zoning of Mg and Na in plagioclase were investigated in detail in order to evaluate the applicability of 26Al– 26Mg chronometer. We conclude that the Al–Mg isotope system of the chondrules in Y-81020 have not been disturbed by parent-body metamorphism and can be used as chronometer assuming homogeneous distribution of 26Al. Assuming an initial 26Al/ 27Al ratio of 5 × 10 −5 in the early solar system, 26Al– 26Mg ages were found to be 1.7–2.5 Ma after CAI formation for Type I, 2.0–3.0 Ma for Type II and 1.9 and 2.6 Ma for Al-rich chondrules. The formation ages of ferromagnesian chondrules in Y-81020 are in good agreement with those of L and LL (type 3.0–3.1) chondrites in the literature, which indicates that common chondrules in the CO chondrite were formed contemporaneously with those in L and LL chondrites. The concurrent formation of chondrules of CO and L/LL chondrites suggests that the chemical differences between CO and L/LL chondrites might be caused by spatial separation of chondrule formation environments in the protoplanetary disk.