The oxygen isotopic properties of olivines in the Semarkona ordinary chondrite

Abstract— In order to explore the origin of chondrules and the chondrites, the O isotopic compositions of nine olivine grains in seven chondrules from the primitive Semarkona LL3.0 chondrite have been determined by ion microprobe. The data plot in the same general region of the three-isotope plot as whole-chondrule samples from ordinary chondrites previously measured by other techniques. There are no significant differences between the O isotopic properties of olivine in the various chondrule groups in the present study, but there is a slight indication that the data plot at the ¹⁶O-rich end of the ordinary chondrite field. This might suggest that the mesostasis contains isotopically heavy O. The olivines in the present study have O isotopic compositions unlike the ¹⁶O-rich olivine grains from the Julesburg ordinary chondrite. Even though olivines in group A chondrules have several properties in common with them, the ¹⁶O-rich Julesburg olivines previously reported are not simply olivines from group A chondrules.     

From whom Bells tolls: Reclassifying Bells among CR chondrites and implications for the formation conditions of CR parent bodies

The ungrouped carbonaceous chondrite (CC) Bells has long been considered petrographically similar to CM chondrites based on its matrix abundance and degree of aqueous alteration, but also shows significant isotopic affinities to CR chondrites. Its taxonomic status is thus important for clarifying the relationship of the CRHB (formerly “CR”) clan with other CCs. In this study, we measured the oxygen isotopic compositions of olivines in type I chondrules and isolated olivine grains in Bells. Bells olivines mostly have ∆¹⁷O > −4‰, similar to CR chondrites but unlike other CCs that are rich in refractory inclusions, in which chondrules are generally richer in ¹⁶O. Therefore, Bells is a CR chondrite (albeit an anomalous one), most similar to the rare, matrix-rich CRs like Al Rais. These chondrites (i) may not necessarily derive from the same primary parent body as mainstream CRs, (ii) bear witness to significant variations of the matrix/chondrule ratio within the CRHB clan, and (iii) may be a good analog for samples retrieved by the space mission OSIRIS-REx.     

Evidence in CO3.0 chondrules for a drift in the O isotopic composition of the solar nebula

Abstract— Several recent studies have shown that materials such as magnetite that formed in asteroids tend to have higher Δ¹⁷O (=δ¹⁷O ? 0.52 × δ¹⁸O) values than those recorded in unaltered chondrules. Other recent studies have shown that, in sets of chondrules from carbonaceous chondrites, Δ¹⁷O tends to increase as the FeO contents of the silicates increase. We report a comparison of the O isotopic composition of olivine phenocrysts in low‐FeO (≤Fa₁) type I and high‐FeO (≥Fa₁₅) type II porphyritic chondrules in the highly primitive CO3.0 chondrite Yamato‐81020. In agreement with a similar study of chondrules in CO3.0 ALH A77307 by Jones et al. (2000), Δ¹⁷O tends to increase with increasing FeO. We find that Δ¹⁷O values are resolved (but only marginally) between the two sets of olivine phenocrysts. In two of the high‐FeO chondrules, the difference between Δ¹⁷O of the late‐formed, high‐FeO phenocryst olivine and those in the low‐FeO cores of relict grains is well‐resolved (although one of the relicts is interpreted to be a partly melted amoeboid olivine inclusion by Yurimoto and Wasson [2002]). It appears that, during much of the chondrule‐forming period, there was a small upward drift in the Δ¹⁷O of nebular solids and that relict cores preserve the record of a different (and earlier) nebular environment.     

Refractory calcium‐aluminum‐rich inclusions and aluminum‐diopside‐rich chondrules in the metal‐rich chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94411

Abstract— The metal‐rich chondrites Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627, contain relatively rare (<1 vol%) calcium‐aluminum‐rich inclusions (CAIs) and Al‐diopside‐rich chondrules. Forty CAIs and CAI fragments and seven Al‐diopside‐rich chondrules were identified in HH 237 and QUE 94411/94627. The CAIs, ～50–400 μm in apparent diameter, include (a) 22 (56%) pyroxene‐spinel ± melilite (+forsterite rim), (b) 11 (28%) forsterite‐bearing, pyroxene‐spinel ± melilite ± anorthite (+forsterite rim) (c) 2 (5%) grossite‐rich (+spinel‐melilite‐pyroxene rim), (d) 2 (5%) hibonite‐melilite (+spinel‐pyroxene ± forsterite rim), (e) 1 (2%) hibonite‐bearing, spinel‐perovskite (+melilite‐pyroxene rim), (f) 1 (2%) spinel‐melilite‐pyroxene‐anorthite, and (g) 1 (2%) amoeboid olivine aggregate. Each type of CAI is known to exist in other chondrite groups, but the high abundance of pyroxene‐spinel ± melilite CAIs with igneous textures and surrounded by a forsterite rim are unique features of HH 237 and QUE 94411/94627. Additionally, oxygen isotopes consistently show relatively heavy compositions with Δ¹⁷O ranging from ?6%0 to ?10%0 (1σ = 1.3%0) for all analyzed CAI minerals (grossite, hibonite, melilite, pyroxene, spinel). This suggests that the CAIs formed in a reservoir isotopically distinct from the reservoir(s) where “normal”, ¹⁶O‐rich (Δ¹⁷O < ?20%0) CAIs in most other chondritic meteorites formed. The Al‐diopside‐rich chondrules, which have previously been observed in CH chondrites and the unique carbonaceous chondrite Adelaide, contain Al‐diopside grains enclosing oriented inclusions of forsterite, and interstitial anorthitic mesostasis and Al‐rich, Ca‐poor pyroxene, occasionally enclosing spinel and forsterite. These chondrules are mineralogically similar to the Al‐rich barred‐olivine chondrules in HH 237 and QUE 94411/94627, but have lower Cr concentrations than the latter, indicating that they may have formed during the same chondrule‐forming event, but at slightly different ambient nebular temperatures. Aluminum‐diopside grains from two Al‐diopside‐rich chondrules have O‐isotopic compositions (Δ¹⁷O ? ?7 ± 1.1 %0) similar to CAI minerals, suggesting that they formed from an isotopically similar reservoir. The oxygen‐isotopic composition of one Ca, Al‐poor cryptocrystalline chondrule in QUE 94411/94627 was analyzed and found to have Δ¹⁷O ? ?3 ± 1.4%0. The characteristics of the CAIs in HH 237 and QUE 94411/94627 are inconsistent with an impact origin of these metal‐rich meteorites. Instead they suggest that the components in CB chondrites are pristine products of large‐scale, high‐temperature processes in the solar nebula and should be considered bona fide chondrites.     

Oxygen isotope systematics of chondrule olivine,pyroxene, and plagioclase in one of the most pristine CV3Red chondrites (Northwest Africa 8613)

We performed in situ oxygen three‐isotope measurements of chondrule olivine, pyroxenes, and plagioclase from the newly described CV_Red chondrite NWA 8613. Additionally, oxygen isotope ratios of plagioclase in chondrules from the Kaba CV3_OxB chondrite were determined to enable comparisons of isotope ratios and degree of alteration of chondrules in both CV lithologies. NWA 8613 was affected by only mild thermal metamorphism. The majority of oxygen isotope ratios of olivine and pyroxenes plot along a slope‐1 line in the oxygen three‐isotope diagram, except for a type II and a remolten barred olivine chondrule. When isotopic relict olivine is excluded, olivine, and low‐ and high‐Ca pyroxenes are indistinguishable regarding Δ¹⁷O values. Conversely, plagioclase in chondrules from NWA 8613 and Kaba plot along mass‐dependent fractionation lines. Oxygen isotopic disequilibrium between phenocrysts and plagioclase was caused probably by exchange of plagioclase with ¹⁶O‐poor fluids on the CV parent body. Based on an existing oxygen isotope mass balance model, possible dust enrichment and ice enhancement factors were estimated. Type I chondrules from NWA 8613 possibly formed at moderately high dust enrichment factors (50× to 150× CI dust relative to solar abundances); estimates for water ice in the chondrule precursors range from 0.2× to 0.6× the nominal amount of ice in dust of CI composition. Findings agree with results from an earlier study on oxygen isotopes in chondrules of the Kaba CV chondrite, providing further evidence for a relatively dry and only moderately high dust‐enriched disk in the CV chondrule‐forming region.     

Oxygen isotopes in forsterite grains from Julesburg and Allende: Oxygen-16-rich material in an ordinary chondrite

Abstract— We have used the Manchester ISOLAB 54 ion microprobe to make in situ measurements of the ¹⁷O/¹⁶O and ¹⁸O/¹⁶O ratios of olivine grains in the Julesburg (L3.6) and Allende (CV3) chondrites. We have discovered a population of olivines in Julesburg characterised by (1) the most ¹⁶O-rich compositions yet reported for olivine from an ordinary chondrite; (2) cores of low-Fa olivine, which frequently shows blue cathodoluminesce; (3) thick coats of more Fa-rich (Fa ～20) olivine, which is also ¹⁶O-enriched. In an O isotopic plot, the Julesburg ¹⁶O-rich grains form a roughly linear array that is offset from the Allende mixing line. The presence of very low Fa olivine and, sometimes, well-defined Fa-rich coats indicates that these grains experienced significantly less thermal metamorphism than most of the olivine in the meteorite. Some ¹⁶O-rich Julesburg grains are associated with minor feldspar or pyroxene and are probably chondrule fragments. They are isotopically indistinguishable from forsterite in Allende; however, Allende forsterite grains do not have the thick Fa20 coats typical of those in Julesburg. These ¹⁶O-rich forsterite grains appear to be related to the “blue olivine” of Steele (1986). Both cores and coats of ¹⁶O-rich grains in Julesburg are isotopically distinct from olivine in Semarkona group A and group B chondrules.     

Oxygen isotope and chemical compositions of magnetite and olivine in the anomalous CK3 Watson 002 and ungrouped Asuka‐881595 carbonaceous chondrites: Effects of parent body metamorphism

We report in situ O isotope and chemical compositions of magnetite and olivine in chondrules of the carbonaceous chondrites Watson‐002 (anomalous CK3) and Asuka (A)‐881595 (ungrouped C3). Magnetite in Watson‐002 occurs as inclusion‐free subhedral grains and rounded inclusion‐bearing porous grains replacing Fe,Ni‐metal. In A‐881595, magnetite is almost entirely inclusion‐free and coexists with Ni‐rich sulfide and less abundant Ni‐poor metal. Oxygen isotope compositions of chondrule olivine in both meteorites plot along carbonaceous chondrite anhydrous mineral (CCAM) line with a slope of approximately 1 and show a range of Δ¹⁷O values (from approximately ?3 to ?6‰). One chondrule from each sample was found to contain O isotopically heterogeneous olivine, probably relict grains. Oxygen isotope compositions of magnetite in A‐881595 plot along a mass‐dependent fractionation line with a slope of 0.5 and show a range of Δ¹⁷O values from ?2.4‰ to ?1.1‰. Oxygen isotope compositions of magnetite in Watson‐002 cluster near the CCAM line and a Δ¹⁷O value of ?4.0‰ to ?2.9‰. These observations indicate that magnetite and chondrule olivine are in O isotope disequilibrium, and, therefore, not cogenetic. We infer that magnetite in CK chondrites formed by the oxidation of pre‐existing metal grains by an aqueous fluid during parent body alteration, in agreement with previous studies. The differences in Δ¹⁷O values of magnetite between Watson‐002 and A‐881595 can be attributed to their different thermal histories: the former experienced a higher degree of thermal metamorphism that led to the O isotope exchange between magnetite and adjacent silicates.     

Correlations and zoning patterns of phosphorus and chromium in olivine from H chondrites and the LL chondrite Semarkona

Phosphorus zoning is observed in olivines in high‐FeO (type IIA) chondrules in H chondrites over the entire range of petrologic grades: H3.1–H6. Features in P concentrations such as oscillatory and sector zoning, and high P cores are present in olivines that are otherwise unzoned in the divalent cations. Aluminum concentrations are low and not significantly associated with P zoning in chondrule olivines. In highly unequilibrated H chondrites, phosphorus zoning is generally positively correlated with Cr. Atomic Cr:P in olivine is roughly 1:1 (3:1 for one zone in one olivine in RC 075), consistent with Cr³⁺ charge‐balancing P⁵⁺ substituting for Si⁴⁺. Normal igneous zonation involving the dominant chrome species Cr²⁺ was observed only in the LL3.0 chondrite Semarkona. In more equilibrated chondrites (H3.5–H3.8), Cr spatially correlated with P is occasionally observed but it is diffuse relative to the P zones. In H4–H6 chondrites, P‐correlated Cr is absent. One signature of higher metamorphic grades (≥H3.8) is the presence of near matrix olivines that are devoid of P oscillatory zoning. The restriction to relatively high metamorphic grade and to grains near the chondrule–matrix interface suggests that this is a response to metasomatic processes. We also observed P‐enriched halos near the chondrule–matrix interface in H3.3–H3.8 chondrites, likely reflecting the loss of P and Ca from mesostasis and precipitation of Ca phosphate near the chondrule surface. These halos are absent in equilibrated chondrites due to coarsening of the phosphate and in unequilibrated chondrites due to low degrees of metasomatism. Olivines in type IA chondrules show none of the P‐zoning ubiquitous in type IIA chondrules or terrestrial igneous olivines, likely reflecting sequestration of P in reduced form within metallic alloys and sulfides during melting of type IA chondrules.     

Mineralogy and petrology of amoeboid olivine inclusions in CO3 chondrites: Relationship to parent‐body aqueous alteration

Abstract— Petrographic and mineralogic studies of amoeboid olivine inclusions (AOIs) in CO3 carbonaceous chondrites reveal that they are sensitive indicators of parent‐body aqueous and thermal alteration. As the petrologic subtype increases from 3.0 to 3.8, forsteritic olivine (Fa_0–1) is systematically converted into ferroan olivine (Fa_60–75). We infer that the Fe, Si and O entered the assemblage along grain boundaries, forming ferroan olivine that filled fractures and voids. As temperatures increased, Fe⁺² from the new olivine exchanged with Mg⁺² from the original AOI to form diffusive haloes around low‐FeO cores. Cations of Mn⁺², Ca⁺² and Cr⁺³ were also mobilized. The systematic changes in AOI textures and olivine compositional distributions can be used to refine the classification of CO3 chondrites into subtypes. In subtype 3.0, olivine occurs as small forsterite grains (Fa_0–1), free of ferroan olivine. In petrologic subtype 3.2, narrow veins of FeO‐rich olivine have formed at forsterite grain boundaries. With increasing alteration, these veins thicken to form zones of ferroan olivine at the outside AOI margin and within the AOI interior. By subtype 3.7, there is a fairly broad olivine compositional distribution in the range Fa_63–70, and by subtype 3.8, no forsterite remains and the high‐Fa peak has narrowed, Fa_64–67. Even at this stage, there is incomplete equilibration in the chondrite as a whole (e.g., data for coarse olivine grains in Isna (CO3.8) chondrules and lithic clasts show a peak at Fa₃₉). We infer that the mineral changes in AOI identified in the low petrologic types required aqueous or hydrothermal fluids whereas those in subtypes ?3.3 largely reflect diffusive exchange within and between mineral grains without the aid of fluids.     

Oxygen isotope characteristics of chondrules from the Yamato‐82094 ungrouped carbonaceous chondrite: Further evidence for common O‐isotope environments sampled among carbonaceous chondrites

High‐precision secondary ion mass spectrometry (SIMS) was employed to investigate oxygen three isotopes of phenocrysts in 35 chondrules from the Yamato (Y) 82094 ungrouped 3.2 carbonaceous chondrite. Twenty‐one of 21 chondrules have multiple homogeneous pyroxene data (?¹⁷O 3SD analytical uncertainty: 0.7‰); 17 of 17 chondrules have multiple homogeneous pyroxene and plagioclase data. Twenty‐one of 25 chondrules have one or more olivine data matching coexisting pyroxene data. Such homogeneous phenocrysts (1) are interpreted to have crystallized from the final chondrule melt, defining host O‐isotope ratios; and (2) suggest efficient O‐isotope exchange between ambient gas and chondrule melt during formation. Host values plot within 0.7‰ of the primitive chondrule mineral (PCM) line. Seventeen chondrules have relict olivine and/or spinel, with some δ¹⁷O and δ¹⁸O values approaching ?40‰, similar to CAI or AOA‐like precursors. Regarding host chondrule data, 22 of 34 have Mg#s of 98.8–99.5 and ?¹⁷O of ?3.9‰ to ?6.1‰, consistent with most Acfer 094, CO, CR, and CV chondrite chondrules, and suggesting a common reduced O‐isotope reservoir devoid of ¹⁶O‐poor H₂O. Six Y‐82094 chondrules have ?¹⁷O near ?2.5‰, with Mg#s of 64–97, consistent with lower Mg# chondrules from Acfer 094, CO, CR, and CV chondrites; their signatures suggest precursors consisting of those forming Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules plus ¹⁶O‐poor H₂O, at high dust enrichments. Three type II chondrules plot slightly above the PCM line, near the terrestrial fractionation line (?¹⁷O: ~+0.1‰). Their O‐isotopes and olivine chemistry are like LL3 type II chondrules, suggesting they sampled ordinary chondrite‐like chondrule precursors. Finally, three Mg# >99 chondrules have ?¹⁷O of ?6.7‰ to ?8.1‰, potentially due to ¹⁶O‐rich refractory precursor components. The predominance of Mg# ~99, ?¹⁷O: ?5‰ ± 1‰ chondrules and a high chondrule‐to‐matrix ratio suggests bulk Y‐82094 characteristics are closely related to anhydrous dust sampled by most carbonaceous chondrite chondrules.     

Geochemical and oxygen isotope perspective of a new R chondrite Dhofar 1671: Affinity with ordinary chondrites

Dhofar 1671 is a relatively new meteorite that previous studies suggest belongs to the Rumuruti chondrite class. Major and REE compositions are generally in agreement with average values of the R chondrites (RCs). Moderately volatile elements such as Se and Zn abundances are lower than the R chondrite values that are similar to those in ordinary chondrites (OCs). Porphyritic olivine pyroxene (POP), radial pyroxene (RP), and barred olivine (BO) chondrules are embedded in a proportionately equal volume of matrix, one of the characteristic features of RCs. Microprobe analyses demonstrate compositional zoning in chondrule and matrix olivines showing Fa‐poor interior and Fa‐rich outer zones. Precise oxygen isotope data for chondrules and matrix obtained by laser‐assisted fluorination show a genetic isotopic relationship between OCs and RCs. On the basis of our data, we propose a strong affinity between these groups and suggest that OC chondrule precursors could have interacted with a ¹⁷O‐rich matrix to form RC chondrules (i.e., ?¹⁷O shifts from ~1‰ to ~3‰). These interactions could have occurred at the same time as “exotic” clasts in brecciated samples formed such as NWA 10214 (LL3–6), Parnallee (LL3), PCA91241 (R3.8–6), and Dhofar 1671 (R3.6). We also infer that the source of the oxidation and ¹⁷O enrichment is the matrix, which may have been enriched in ¹⁷O‐rich water. The abundance of matrix in RCs relative to OCs, ensured that these rocks would be apparently more oxidized and appreciably ¹⁷O‐enriched. In situ analysis of Dhofar 1671 is recommended to further strengthen the link between OCs and RCs.     

Refractory forsterite in primitive meteorites: Condensates from the solar nebula?

Abstract— All groups of chondritic meteorites contain discrete grains of forsteritic olivine with FeO contents below 1 wt% and high concentrations of refractory elements such as Ca, Al, and Ti. Ten such grains (52 to 754 μg) with minor amounts of adhering matrix were separated from the Allende meteorite. After bulk chemical analysis by instrumental neutron activation analysis (INAA), some samples were analyzed with an electron microprobe and some with an ion microprobe. Matrix that accreted to the forsterite grains has a well‐defined unique composition, different from average Allende matrix in having higher Cr and lower Ni and Co contents, which implies limited mixing of Allende matrix. All samples have approximately chondritic relative abundances of refractory elements Ca, Al, Sc, and rare‐earth elements (REE), although some of these elements, such as Al, do not quantitatively reside in forsterite; whereas others (e.g., Ca) are intrinsic to forsterite. The chondritic refractory element ratios in bulk samples, the generally high abundance level of refractory elements, and the presence of Ca‐Al‐Ti‐rich glass inclusions suggest a genetic relationship of refractory condensates with forsteritic olivine. The Ca‐Al‐Ti‐rich glasses may have acted as nuclei for forsterite condensation. Arguments are presented that exclude an origin of refractory forsterite by crystallization from melts with compositions characteristic of Allende chondrules: (a) All forsterite grains have CaO contents between 0.5 and 0.7 wt% with no apparent zoning, requiring voluminous parental melts with 18 to 20 wt% CaO, far above the average CaO content of Allende chondrules. Similar arguments apply to Al contents. (b) The low FeO content of refractory forsterite of 0.2‐0.4 wt% imposes an upper limit of ～1 wt% of FeO on the parental melt, too low for ordinary and carbonaceous chondrule melts, (c) The Mn contents of refractory forsterites are between 30 to 40 ppm. This is at least one order of magnitude below the Mn content of chondrule olivines in all classes of meteorites. The observed Mn contents of refractory forsterite are much too low for equilibrium between olivine and melts of chondrule composition, (d) As shown earlier, refractory forsterites have O‐isotopic compositions different from chondrules (Weinbruch et al., 1993a). Refractory olivines in carbonaceous chondrites are found in matrix and in chondrules. The compositional similarity of both types was taken to indicate that all refractory forsterites formed inside chondrules (e.g., Jones, 1992). As refractory forsterite cannot have formed by crystallization from chondrule melts, we conclude that refractory forsterite from chondrules are relic grains that survived chondrule melting and probably formed in the same way as refractory forsterite enclosed in matrix. We favor an origin of refractory forsterite by condensation from an oxidized nebular gas.     

Origin of isolated olivine grains in carbonaceous chondrites

We report microscopic, cathodoluminescence, chemical, and O isotopic measurements of FeO‐poor isolated olivine grains (IOG) in the carbonaceous chondrites Allende (CV3), Northwest Africa 5958 (C2‐ung), Northwest Africa 11086 (CM2‐an), and Allan Hills 77307 (CO3.0). The general petrographic, chemical, and isotopic similarity with bona fide type I chondrules confirms that the IOG derived from them. The concentric CL zoning, reflecting a decrease in refractory elements toward the margins, and frequent rimming by enstatite are taken as evidence of interaction of the IOG with the gas as stand‐alone objects. This indicates that they were splashed out of chondrules when these were still partially molten. CaO‐rich refractory forsterites, which are restricted to ?¹⁷O <?4‰ likely escaped equilibration at lower temperatures because of their large size and possibly quicker quenching. The IOG thus bear witness to frequent collisions in the chondrule‐forming regions.     

Anorthite‐rich chondrules in CR and CH carbonaceous chondrites: Genetic link between calcium‐aluminum‐rich inclusions and ferromagnesian chondrules

Abstract— Anorthite‐rich chondrules in CR and CH carbonaceous chondrites consist of magnesian low‐Ca pyroxene and forsterite phenocrysts, FeNi‐metal nodules, interstitial anorthite, Al‐Ti‐Cr‐rich low‐Ca and high‐Ca pyroxenes, and crystalline mesostasis composed of silica, anorthite and high‐Ca pyroxene. Three anorthite‐rich chondrules contain relic calcium‐aluminum‐rich inclusions (CAIs) composed of anorthite, spinel, ±Al‐diopside, and ± forsterite. A few chondrules contain regions which are texturally and mineralogically similar to magnesian (type I) chondrules and consist of forsterite, low‐Ca pyroxene and abundant FeNi‐metal nodules. Anorthite‐rich chondrules in CR and CH chondrites are mineralogically similar to those in CV and CO carbonaceous chondrites, but contain no secondary nepheline, sodalite or ferrosilite. Relatively high abundances of moderately‐volatile elements such as Cr, Mn and Si in the anorthite‐rich chondrules suggest that these chondrules could not have been produced by volatilization of the ferromagnesian chondrule precursors or by melting of the refractory materials only. We infer instead that anorthite‐rich chondrules in carbonaceous chondrites formed by melting of the reduced chondrule precursors (olivine, pyroxenes, FeNi‐metal) mixed with the refractory materials, including relic CAIs, composed of anorthite, spinel, high‐Ca pyroxene and forsterite. The observed mineralogical and textural similarities of the anorthite‐rich chondrules in several carbonaceous chondrite groups (CV, CO, CH, CR) may indicate that these chondrules formed in the region(s) intermediate between the regions where CAIs and ferromagnesian chondrules originated. This may explain the relative enrichment of anorthite‐rich chondrules in ¹⁶O compared to typical ferromagnesian chondrules (Russell et al., 2000).     

Origin of fayalitic olivine rims and lath-shaped matrix olivine in the CV3 chondrite Allende and its dark inclusions

Abstract— We have studied an Allende dark inclusion by optical microscopy, scanning electron microscopy, electron microprobe analysis and transmission electron microscopy. The inclusion consists of chondrules, isolated olivines and matrix, which, as in the Allende host, is mainly composed of 5–20 μm long lath-shaped fayalitic grains with a narrow compositional range (Fa_{42 ± 2}) and nepheline. Olivine phenocrysts in chondrules and isolated olivine grains show various degrees of replacement by 5–10 μm wide fayalitic rims (Fa_{39 ± 2}) and 100–1000 μm wide translucent zones, which consist of 5–20 μm long lath-shaped fayalitic grains (Fa_{41 ± 1}) intergrown with nepheline. These fayalitic olivines, like those in the matrix of the dark inclusion, contain 10–20 nm sized inclusions of chromite, hercynite, and Fe-Ni sulfides. The fayalitic rims around remnant olivines are texturally and compositionally identical to those in Allende host, suggesting that they have similar origins. Chondrules are surrounded by opaque rims consisting of tiny lath-shaped fayalitic olivines (<1–3 μm long) intergrown with nepheline. As in the Allende host, fayalitic olivine veins may crosscut altered chondrules, fine-grained chondrule rims and extend into the matrix, indicating that alteration occurred after accretion. We infer that fayalitic olivine rims and lath-shaped fayalites in Allende and its dark inclusions formed from phyllosilicate intermediate phases. This explanation accounts for (1) the similarity of the replacement textures observed in the dark inclusion and Allende host to aqueous alteration textures in CM chondrites; (2) the anomalously high abundances of Al and Cr and the presence of tiny inclusions of spinels and sulfides in fayalitic olivines in Allende and Allende dark inclusions; (3) abundant voids and defects in lath-shaped fayalites in the Allende dark inclusion, which may be analogous to those in partly dehydrated phyllosilicates in metamorphosed CM/CI chondrites. We conclude that the matrix and chondrule rims in Allende were largely converted to phyllosilicates and then completely dehydrated. The Allende dark inclusions experienced diverse degrees of aqueous/hydrothermal alteration prior to complete dehydration. The absence of low-Ca pyroxene in the dark inclusion and its significant replacement by fayalitic olivine in Allende is consistent with the lower resistance of low-Ca pyroxene to aqueous alteration relative to forsteritic olivine. Hydro-thermal processing of Allende probably also accounts for the low abundance of planetary noble gases and interstellar grains, and the formation of nepheline, sodalite, salite-hedenbergite pyroxenes, wollastonite, kirschsteinite and andradite in chondrules and Ca,Al-rich inclusions.     

Olivine dissolution in molten silicates: An experimental study with application to chondrule formation

Mg‐rich olivine is a ubiquitous phase in type I porphyritic chondrules in various classes of chondritic meteorites. The anhedral shape of olivine grains, their size distribution, as well as their poikilitic textures within low‐Ca pyroxene suggest that olivines suffer dissolution during chondrule formation. Owing to a set of high‐temperature experiments (1450–1540 °C) we determined the kinetics of resorption of forsterite in molten silicates, using for the first time X‐ray microtomography. Results indicate that forsterite dissolution in chondrule‐like melts is a very fast process with rates that range from ~5 μm min^?1 to ~22 μm min^?1. Forsterite dissolution strongly depends on the melt composition, with rates decreasing with increasing the magnesium and/or the silica content of the melt. An empirical model based on forsterite saturation and viscosity of the starting melt composition successfully reproduces the forsteritic olivine dissolution rates as a function of temperature and composition for both our experiments and those of the literature. Application of our results to chondrules could explain the textures of zoned type I chondrules during their formation by gas‐melt interaction. We show that the olivine/liquid ratio on one hand and the silica entrance from the gas phase (SiO_g) into the chondrule melt on the other hand, have counteracting effects on the Mg‐rich olivine dissolution behavior. Silica entrance would favor dissolution by maintaining disequilibrium between olivine and melt. Hence, this would explain the preferential dissolution of olivine as well as the preferential abundances of pyroxene at the margins of chondrules. Incipient dissolution would also occur in the silica‐poorer melt of chondrule core but should be followed by crystallization of new olivine (overgrowth and/or newly grown crystals). While explaining textures and grain size distributions of olivines, as well as the centripetal distribution of low‐Ca pyroxene in porphyritic chondrules, this scenario could also be consistent with the diverse chemical, isotopic, and thermal conditions recorded by olivines in a given chondrule.     

Oxygen and magnesium isotopic compositions of amoeboid olivine aggregates from the Semarkona LL3.0 chondrite

Abstract— Amoeboid olivine aggregates (AOAs) in the LL3.0 Semarkona chondrite have been studied by secondary ion mass spectrometry. The AOAs mainly consist of aggregates of olivine grains with interstitial Al‐Ti‐rich diopside and anorthite. Oxygen‐isotopic compositions of all phases are consistently enriched in ¹⁶O, with δ^17,18O = ～?50‰. The initial ²⁶Al/²⁷Al ratios are calculated to be 5.6 ± 0.9 (2σ) × 10^?5. These values are equivalent to those of AOAs and fine‐grained calcium‐aluminum‐rich inclusions (FGIs) from pristine carbonaceous chondrites. This suggests that AOAs in ordinary chondrites formed in the same ¹⁶O‐rich calcium‐aluminum‐rich inclusion (CAI)‐forming region of the solar nebula as AOAs and FGIs in carbonaceous chondrites, and subsequently moved to the accretion region of the ordinary chondrite parent body in the solar nebula.     

Bo Xian (LL3.9): Oxygen‐isotopic and mineralogical characterisation of separated chondrules

Abstract— We report the results of a mineralogical and O‐isotopic study of 362 chondrules disaggregated from the Bo Xian chondrite. The range of mineral compositions (Fa = 0.8–31.2%, mean = 23.5%, mode = 27–28%) are consistent with a reclassification of this meteorite from LL4 to LL3.9. Chondrule diameters range from 0.20 to 3.40 mm (mean = 0.74 mm) in the disaggregated population. A lower mean diameter (0.64 mm) calculated from thin‐section measurements partly reflects the high proportion of chondrule fragments. The chondrule size distribution, which is approximately log‐normal, is consistent with size‐sorting mechanisms. This sorting could be linked to the fragmentation of many chondrules on the parent body. However, in detail, the variation in diameter of different chondrule types and a hiatus in the size distribution at 0.6 mm indicate that there may have been complex controls perhaps partly being determined by the chondrule formation mechanism. Seven percent of the sectioned chondrules (102) contain chemically fractionated mineral assemblages: cristobalite‐bearing and Al‐rich. This significant degree of chemical heterogeneity probably resulted from both igneous and volatility controls. Oxygen‐isotopic compositions were determined on mineral separates and 16 of the sectioned chondrules. Three separate isotopic exchange events have been identified. The dominant one is a low‐temperature hydrous gas‐solid exchange event between ¹⁶O‐rich solid and ¹⁶O‐poor gas reservoirs that lay along a slope 1.0 line on three‐isotope plots. Partial equilibration with the gas by feldspar and cristobalite, which exchanged more rapidly than olivine or pyroxene, led to formation of a slope 0.77 mixing line for Bo Xian and other LL chondrites. Mineralogy is the dominant control on the extent of this exchange; no relationship between isotopic composition and chondrule texture or size was identified. The feldspar separate and cristobalite‐rich chondrules have the most ¹⁶O‐poor compositions. Subsequently, thermal metamorphism in the parent body led to partial isotopic equilibration between the different mineral phases. A third exchange event, predating the other two events, is probably shown by one of the Al‐rich chondrules. This has an ¹⁶O‐rich composition, lying below the terrestrial fractionation line. Another Al‐rich chondrule has a normal ordinary chondrite isotopic composition. It is not clear whether the isotopic fractionation recorded in some Al‐rich chondrules can be achieved by the dominant gas‐solid exchange. Instead, the precursor O to the mineral phases may have become ¹⁶O‐rich during an earlier phase of mass‐independent fractionation.     

Mineralogical characterization of primitive,type‐3 lithologies in Rumuruti chondrites

Abstract— Rumuruti (R) chondrites constitute a new, well‐established chondrite group different from the carbonaceous, ordinary, and enstatite chondrites. Many of these samples are gas‐rich regolith breccias showing the typical light‐dark structure and consist of abundant fragments of various parent‐body lithologies embedded in a fine‐grained olivine‐rich matrix. Unequilibrated type‐3 lithologies among these fragments have frequently been mentioned in various publications. In this study, detailed mineralogical data on seven primitive fragments from the R‐chondrites Dar al Gani 013 and Hughes 030 are presented. The fragments range from ～300 μ in size up to several millimeters. Generally, the main characteristics can be summarized as follows: (1) Unequilibrated type‐3 fragments have a well‐preserved chondritic texture with a chondrule‐to‐matrix ratio of ～1:1. Chondrules and chondrule fragments are embedded in a fine‐grained olivine‐rich matrix. Thus, the texture is quite similar to that of type‐3 carbonaceous chondrites. (2) In all cases, matrix olivines in type‐3 fragments have a significantly higher Fa content (44–57 mol%) than olivines in other (equilibrated) lithologies (38–40 mol% Fa). (3) Olivines and pyroxenes occurring within chondrules or as fragments are highly variable in composition (Fa_0–65 and Fs_0–33, respectively) and, generally, more magnesian than those found in equilibrated R chondrites. Agglomerated material of the R‐chondrite parent body (or bodies) was highly unequilibrated. It is suggested that the material that accreted to form the parent body consisted of chondrules and chondrule fragments, mainly having Mg‐rich silicate constituents, and Fe‐rich highly oxidized fine‐grained materials. The dominating phase of this fine‐grained material may have been Fa‐rich olivine from the beginning. The brecciated whole rocks, the R‐chondrite regolith breccias, were not significantly reheated subsequent to brecciation or during lithification, as indicated by negligible degree of equilibration between matrix components and Mg‐rich olivines and pyroxenes in primitive type‐3 fragments.     

Oxygen isotopes in magnetite and fayalite in CV chondrites Kaba and Mokoia

Abstract— We report in situ measurements of O‐isotopic compositions of magnetite and primary and secondary olivine in the highly unequilibrated oxidized CV chondrites Kaba and Mokoia. In both meteorites, the magnetite and the secondary olivine (fayalite, Fa_90–100) have O‐isotopic compositions near the terrestrial fractionation (TF) line; the mean Δ¹⁷O (= δ¹⁷O‐0.52 × δ¹⁸O) value is about ?1%‰. In contrast, the compositions of nearby primary (chondrule), low‐FeO olivines (Fa_1–2) are well below the TF line; Δ¹⁷O values range from ?3 to ?9%‰. Krot et al. (1998) summarized evidence indicating that the secondary phases in these chondrites formed by aqueous alteration in an asteroidal setting. The compositions of magnetite and fayalite in Kaba and Mokoia imply that the O‐isotopic composition of the oxidant was near or somewhat above the TF line. In Mokoia the fayalite and magnetite differ in δ¹⁸O by ～20%‰, whereas these same materials in Kaba have virtually identical compositions. The difference between Mokoia magnetite and fayalite may indicate formation in isotopic equilibrium in a water‐rich environment at low temperatures, ～300 K. In contrast, the similar compositions of these phases in Kaba may indicate formation of the fayalite by replacement of preexisting magnetite in dry environment, with the O coming entirely from the precursor magnetite and silica. The Δ¹⁷O of the oxidant incorporated into the CV parent body (as phyllosilicates or H₂O) appears to have been much (7–8%‰) lower than that in that incorporated into the LL parent body (Choi et al, 1998), which suggests that the O‐isotopic composition of the nebular gas was spatially or temporally variable.