A new mineralogical approach for CO3 chondrite characterization by X-ray diffraction: Identification of primordial phases and thermal history

Using the in-plane rotation of polished thin section, the X-ray diffraction patterns exhibiting a high degree of randomness similar to powder pattern were obtained for 10 CO3 chondrites, which distinguished 130 reflections of olivine in the chondrules from that in the matrix, and showed systematic differences among subtypes based on the full width at half maximum intensity of two olivine 130 peaks. A lower petrologic subtype is characterized by sharp and strong peaks for forsteritic olivines in type I chondrules and by a weak and broad peak for ferroan matrices, and the higher petrologic subtypes are characterized by sharp and strong peaks for recrystallized matrices and a weakened or absent peak of magnesian olivines. The systematic change in the split peak of olivine 130 was linked with the mean diffusion length of Mg-Fe in olivine phenocrysts in type I chondrules. Fe-Ni diffusion in metals was considered to estimate the peak temperature of CO3.0, near the surface on the parent body. The peak metamorphic temperatures were estimated to be ~600–910 K using the onion-shell model when the cooling time was 10⁶–10⁸ yr on the parent body. A weak peak for ferroan olivine of CO3.0 suggests the amorphous silicate in matrices. The modal abundance of the amorphous Fe-silicate for subtype 3.0 (15% for Allan Hills [ALH] 77307 and 9% for Yamato [Y]-81020) was also evaluated from the deviation in trend of the relative peak ratios of the Fe-rich (≥Fa₂₅) and Mg-rich (<Fa₂₅) olivines for subtypes. The existence of martensites was suggested for ALH 77307. Amorphous silicate in matrices is a more resistant primordial component that produced the CO3 chondrites than martensite.     

Oxygen isotopes in chondrule olivine and isolated olivine grains from the CO3 chondrite Allan Hills A77307

Abstract— We have measured O‐isotopic ratios in a variety of olivine grains in the CO3 chondrite Allan Hills (ALH) A77307 using secondary ion mass spectrometry in order to study the chondrule formation process and the origin of isolated olivine grains in unequilibrated chondrites. Oxygen‐isotopic ratios of olivines in this chondrite are variable from δ¹⁷O = ?15.5 to +4.5% and δ¹⁸O = ?11.5 to +3.9%, with Δ¹⁷O varying from ?10.4 to +3.5%. Forsteritic olivines, Fa_<1, are enriched in ¹⁶O relative to the bulk chondrite, whereas more FeO‐rich olivines are more depleted in ¹⁶O. Most ratios lie close to the carbonaceous chondrite anhydrous minerals (CCAM) line with negative values of Δ¹⁷O, although one grain of composition Fa₄ has a mean Δ¹⁷O of +1.6%. Marked O‐isotopic heterogeneity within one FeO‐rich chondrule is the result of incorporation of relic, ¹⁶O‐rich, Mg‐rich grains into a more ¹⁶O‐depleted host. Isolated olivine grains, including isolated forsterites, have similar O‐isotopic ratios to olivine in chondrules of corresponding chemical composition. This is consistent with derivation of isolated olivine from chondrules, as well as the possibility that isolated grains are chondrule precursors. The high ¹⁶O in forsteritic olivine is similar to that observed in forsterite in CV and CI chondrites and the ordinary chondrite Julesburg and suggests nebula‐wide processes for the origin of forsterite that appears to be a primitive nebular component.     

Correlated petrologic and geochemical characteristics of CO3 chondrites

Abstract— Many properties of CO3 chondrites have been shown previously to have resulted from thermal metamorphism; petrologic subtypes 3.0–3.7 have been assigned to members of the group. Additional properties that correlate with the metamorphic sequence but seem to have resulted from hydrothermal alteration include the modal abundance of amoeboid olivine inclusions (AOI), chondrule size, the types of refractory inclusions and whole rock O isotopic composition. The percentage of rimmed AOI increases with petrologic subtype. The rims most likely formed during hydrothermal alteration. The previously reported correlation between AOI abundance and chondrite subtype is probably an artifact due to the difficulty in recognizing small unrimmed AOI in the least metamorphosed CO3 chondrites. Because large (≥ 200 μm size) porphyritic chondrules have nearly the same mean size in all CO3 chondrites, it seems likely that the correlation between chondrule size and subtype is due to alteration of the smallest chondrules to the point of unrecogizability as complete objects in the more metamorphosed CO3 chondrites. The previously reported decrease in the proportion of melilite-rich refractory inclusions with increasing petrologic subtype may have resulted from more extensive hydrothermal alteration in CO3.4–3.7 chondrites that converted primary melilite into Ca-pyroxene, andradite and nepheline. Alteration probably caused the preferential occurrence of ¹⁶O-poor oxygen isotopes in the more metamorphosed whole rock samples.     

An amoeboid olivine inclusion (AOI) in CK3 NWA 1559, comparison to AOIs in CV3 Allende,and the origin of AOIs in CK and CV chondrites

An amoeboid olivine inclusion in CK3 NWA 1559 (0.54 × 1.3 mm) consists of a diopside‐rich interior (approximately 35 vol%) and an olivine‐rich rim (approximately 65 vol%). It is the first AOI to be described in CK chondrites; the apparent paucity of these inclusions is due to extensive parent‐body recrystallization. The AOI interior contains irregular 3–15 μm‐sized Al‐bearing diopside grains (approximately 70 vol%), 2–20 μm‐sized pores (approximately 30 vol%), and traces of approximately 2 μm plagioclase grains. The 75–160 μm‐thick rim contains 20–130 μm‐sized ferroan olivine grains, some with 120º triple junctions. A few coarse (25–50 μm‐sized) patches of plagioclase with 2–18 μm‐thick diopside rinds occur in several places just beneath the rim. The occurrence of olivine rims around AOI‐1 and around many AOIs in CV3 Allende suggests that CK and CV AOIs formed by the acquisition of porous forsteritic rims around fine‐grained, rimless CAIs that consisted of diopside, anorthite, melilite, and spinel. Individual AOIs in carbonaceous chondrites may have formed after transient heating events melted their olivine rims as well as portions of the underlying interiors. In AOI‐1, coarse plagioclase grains with diopside rinds crystallized immediately below the olivine rim. Secondary parent‐body alteration transformed forsterite in the rims of CV and CK AOIs into more‐ferroan olivine. Some of the abundant pores in the interior of AOI‐1 may have formed during aqueous alteration after fine‐grained melilite and anorthite were leached out. Chondrite groups with large chondrules tend to have large AOIs. AOIs that formed in dust‐rich nebular regions (where CV and CK chondrites later accreted) tend to be larger than AOIs from less‐dusty regions.     

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.     

Heavily metamorphosed clasts from the CV chondrite breccias Mokoia and Yamato‐86009

Abstract– Metamorphosed clasts in the CV carbonaceous chondrite breccias Mokoia and Yamato‐86009 (Y‐86009) are coarse‐grained, granular, polymineralic rocks composed of Ca‐bearing (up to 0.6 wt% CaO) ferroan olivine (Fa_34–39), ferroan Al‐diopside (Fs_9–13Wo_47–50, approximately 2–7 wt% Al₂O₃), plagioclase (An_37–84Ab_63–17), Cr‐spinel (Cr/(Cr + Al) = 0.19–0.45, Fe/(Fe + Mg) = 0.60–0.79), nepheline, pyrrhotite, pentlandite, Ca‐phosphate, and rare grains of Ni‐rich taenite; low‐Ca pyroxene is absent. Most clasts have triple junctions between silicate grains, indicative of prolonged thermal annealing. Based on the olivine‐spinel and pyroxene thermometry, the estimated metamorphic temperature recorded by the clasts is approximately 1100 K. Few clasts experienced thermal metamorphism to a lower degree and preserved chondrule‐like textures. The Mokoia and Y‐86009 clasts are mineralogically unique and different from metamorphosed chondrites of known groups (H, L, LL, R, EH, EL, CO, CK) and primitive achondrites (acapulcoites, brachinites, lodranites). On a three‐isotope oxygen diagram, compositions of olivine in the clasts plot along carbonaceous chondrite anhydrous mineral line and the Allende mass‐fractionation line, and overlap with those of the CV chondrule olivines; the Δ¹⁷O values of the clasts range from about ?4.3‰ to ?3.0‰. We suggest that the clasts represent fragments of the CV‐like material that experienced metasomatic alteration, high‐temperature metamorphism, and possibly melting in the interior of the CV parent asteroid. The lack of low‐Ca pyroxene in the clasts could be due to its replacement by ferroan olivine during iron‐alkali metasomatic alteration or by high‐Ca ferroan pyroxene during melting under oxidizing conditions.     

Compositional diversity of ordinary chondrites inferred from petrology,bulk chemical,and oxygen isotopic compositions of the lowest FeO ordinary chondrite,Yamato 982717

We performed a petrologic, geochemical, and oxygen isotopic study of the lowest FeO ordinary chondrite (OC), Yamato (Y) 982717. Y 982717 shows a chondritic texture composed of chondrules and chondrule fragments, and mineral fragments set in a finer grained, clastic matrix, similar to H4 chondrites. The composition of olivine (Fa_{11.17 ± 0.48 (1σ)}) and low‐Ca pyroxene (Fs_{11.07 ± 0.98 (1σ)}Wo_{0.90 ± 0.71(1σ)}) is significantly more magnesian than those of typical H chondrites (Fa_16.0‐20, Fs_14.5‐18.0), as well as other known low‐FeO OCs (Fa_12.8‐16.7; Fs_13‐16). However, the bulk chemical composition of Y 982717, in particular lithophile and moderately volatile elements, is within the range of OCs. The bulk siderophile element composition (Ni, Co) is within the range of H chondrites and distinguishable from L chondrites. The O‐isotopic composition is also within the range of H chondrites. The lack of reduction textures indicates that the low olivine Fa content and low‐Ca pyroxene Fs content are characteristics of the precursor materials, rather than the result of reduction during thermal metamorphism. We suggest that the H chondrites are more compositionally diverse than has been previously recognized.     

Pecora Escarpment 91002: A member of the new Rumuruti (R) chondrite group

Abstract— Pecora Escarpment (PCA)91002 is a light/dark-structured chondrite breccia related to Carlisle Lakes and Rumuruti; the meteorite contains ～10–20 vol% equilibrated (type ?5 and ?6) clasts within a clastic groundmass, much of which was metamorphosed to type-3.8 levels. The olivine compositional distribution forms a tight cluster that peaks at Fa_38–40; by contrast, low-Ca pyroxene compositions are highly variable. Opaque phases identified in PCA91002 and its paired specimen, PCA91241, include pyrrhotite, pentlandite, pyrite, chromite, ilmenite, metallic Cu and magnetite. The majority of the rock is of shock stage S3-S4; there are numerous sulfide-rich shock veins and 50-μm plagioclase melt pockets. Instrumental neutron activation analysis shows that, unlike Carlisle Lakes and ALH85151, PCA91002 exhibits no Ca enrichment or Au depletion; because PCA91002 is relatively unweathered, it seems probable that the Ca and Au fractionations in Carlisle Lakes and ALH85151 were caused by terrestrial alteration. The Rumuruti-like (formerly Carlisle-Lakes-like) chondrites now include eight separate meteorites. Their geochemical and petrographic similarities suggest that they constitute a distinct chondrite group characterized by unfractionated refractory lithophile abundances (0.95 ± 0.05x CI), high bulk Δ¹⁷O, a low chondrule/groundmass modal abundance ratio, mean chondrule diameters in the 400 ± 100 μm range, abundant NiO-bearing ferroan olivine, sodic plagioclase, titanian chromite, abundant pyrrhotite and pentlandite and negligible metallic Fe-Ni. We propose that this group be called R chondrites after Rumuruti, the only fall. The abundant NiO-bearing ferroan olivine grains, the occurrence of Cu-bearing sulfide, and the paucity of metallic Fe-Ni indicate that R chondrites are highly oxidized. It is unlikely that appreciable oxidation took place on the parent body because of the essential lack of plausible oxidizing agents (e.g., magnetite or hydrated silicates). Therefore, oxidation of R chondrite material must have occurred in the nebula. A few type-I porphyritic olivine chondrules containing olivine grains with cores of Fa_3–4 composition occur in PCA91002; these chondrules probably formed initially as metallic-Fe-Ni-bearing objects at high nebular temperatures. As temperatures decreased and more metallic Fe was oxidized, these chondrules accreted small amounts of oxidized material and were remelted. The ferroan compositions of the >5-μm olivine grains in the R chondrites reflect equilibration with fine-grained FeO-rich matrix material during parent body metatnorphism.     

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.     

Evidence for low‐temperature growth of fayalite and hedenbergite in MacAlpine Hills 88107, an ungrouped carbonaceous chondrite related to the CM‐CO clan

Abstract— The carbonaceous chondrite MacAlpine Hills (MAC) 88107 has bulk composition and mineralogy that are intermediate between those of CO and CM chondrites. This meteorite experienced minor alteration and a low degree of thermal metamorphism (petrologic type 3.1) and escaped post‐accretional brecciation. The alteration resulted in the formation of fayalite (Fa_90–100). Al‐free hedenbergite (～Fs₅₀Wo₅₀), phyllosilicates (saponite‐serpentine intergrowths), magnetite, and Ni‐bearing sulfides (pyrrhotite and pentlandite). Fayalite and hedenbergite typically occur as veins, which start at the opaque nodules in the chondrule peripheries, crosscut fine‐grained rims and either terminate at the boundaries with the neighboring fine‐grained rims or continue as layers between these rims. These observations suggest that fayalite and hedenbergite crystallized after accretion and compaction of the fine‐grained rims. Fayalite also overgrows isolated forsteritic (Fa_1–5) and fayalitic (Fa_20–40) olivine grains without any evidence for Fe‐Mg interdiffusion; it also replaces massive magnetite‐sulfide grains. The initial ⁵³Mn/⁵⁵Mn ratio of (1.58 ± 0.26) × 10^?6 in the MAC 88107 fayalite corresponds to an age difference between the formation of fayalite and refractory inclusions in Allende of either ～9 or 18 Ma, depending upon the value of the solar system initial abundance of ⁵³Mn used in age calculations. Formation of secondary fayalite and hedenbergite requires mobilization and transport of Ca, Si, and Fe either through a high‐temperature gaseous phase (Hua and Buseck, 1995) or low‐temperature aqueous solution (Krot et al., 1998a, b). The high‐temperature nebular model for the origin of fayalite (Hua and Buseck, 1995) fails to explain (a) formation of fayalite‐hedenbergite assemblages after accretion of fine‐grained rims that lack any evidence for high‐temperature processing; (b) extreme fractionation of refractory lithophile elements of similar volatility, Ca and Al, in hedenbergite; and (c) absence of Fe‐Mg interdiffusion along fayalite‐forsterite boundaries. We conclude that fayalite and hedenbergite in MAC 88107 formed during late‐stage, low‐temperature (approximately 150–200 °C) aqueous alteration. The data for MAC 88107 extend the evidence for an early onset of aqueous activity on chondrite parent bodies and reinforce the conclusion that liquid water played an important role in the chemical and mineralogical evolution of the first chondritic planetesimals.     

Petrology and oxygen isotopic compositions of calcium‐aluminum‐rich inclusions in primitive CO3.0‐3.1 chondrites

The petrologic and oxygen isotopic characteristics of calcium‐aluminum‐rich inclusions (CAIs) in CO chondrites were further constrained by studying CAIs from six primitive CO3.0‐3.1 chondrites, including two Antarctic meteorites (DOM 08006 and MIL 090010), three hot desert meteorites (NWA 10493, NWA 10498, and NWA 7892), and the Colony meteorite. The CAIs can be divided into hibonite‐bearing inclusions (spinel‐hibonite spherules, monomineralic grains, hibonite‐pyroxene microspherules, and irregular/nodular objects), grossite‐bearing inclusions (monomineralic grains, grossite‐melilite microspherules, and irregular/nodular objects), melilite‐rich inclusions (fluffy Type A, compact type A, monomineralic grains, and igneous fragments), spinel‐pyroxene inclusions (fluffy objects resembling fine‐grained spinel‐rich inclusions in CV chondrites and nodular/banded objects resembling those in CM chondrites), and pyroxene‐anorthite inclusions. They are typically small (98.4 ± 54.4 µm, 1SD) and comprise 1.54 ± 0.43 (1SD) area% of the host chondrites. Melilite in the hot desert and Colony meteorites was extensively replaced by a hydrated Ca‐Al‐silicate during terrestrial weathering and converted melilite‐rich inclusions into spinel‐pyroxene inclusions. The CAI populations of the weathered COs are very similar to those in CM chondrites, suggesting that complete replacement of melilite by terrestrial weathering, and possibly parent body aqueous alteration, would make the CO CAIs CM‐like, supporting the hypothesis that CO and CM chondrites derive from similar nebular materials. Within the CO3.0‐3.1 chondrites, asteroidal alteration significantly resets oxygen isotopic compositions of CAIs in CO3.1 chondrites (?¹⁷O: ?25 to ?2‰) but left those in CO3.0‐3.05 chondrites mostly unchanged (?¹⁷O: ?25 to ?20‰), further supporting the model whereby thermal metamorphism became evident in CO chondrites of petrologic type ≥3.1. The resistance of CAI minerals to oxygen isotope exchange during thermal metamorphism follows in the order: melilite + grossite < hibonite + anorthite < spinel + diopside + forsterite. Meanwhile, terrestrial weathering destroys melilite without changing the chemical and isotopic compositions of melilite and other CAI minerals.     

THE KRAMER CREEK,COLORADO METEORITE: A NEW L4 CHONDRITE

The Kramer Creek, Colorado, chondrite was found in 1966 and identified as a meteorite in 1972. Bulk chemical analysis, particularly the total iron content (20.36%) and the ratio of Fe_total/SiO₂ (0.52), as well as the compositions of olivine (Fa_21.7) and orthopyroxene (Fs_18.3) place the meteorite into the L-group of chondrites. The well-defined chondritic texture of the meteorite, the presence of igneous glass in the chondrules and of low-Ca clinopyroxene, as well as the slight variations in FeO contents of olivine (2.4% MD) and orthopyroxene (5.6% MD) indicate that the chondrite belongs to the type 4 petrologic class.     

Fe‐Mg interdiffusion profiles in rimmed forsterite grains in the Allende matrix: Time–temperature constraints for the parent body metamorphism

The Allende matrix is dominated by micron‐sized lath‐shaped fayalitic olivine grains with a narrow compositional range (Fa_40–50). Fayalitic olivines also occur as rims around forsterite grains in chondrules and isolated forsterite fragments in the matrix or as veins cross‐cutting the grains. Allende is a type 3 CV carbonaceous chondrite having experienced a moderate thermal metamorphism. There is therefore a strong chemical disequilibrium between the large forsterite grains and the fayalite‐rich fine‐grained matrix. Chemical gradients at interfaces are poorly developed and thus not accessible using conventional techniques. Here, we used analytical transmission electron microscopy to study the microstructure of the fayalite‐rich matrix grains and interfaces with forsterite fragments. We confirm that fayalitic grains in the matrix and fayalitic rims around forsterite fragments have the same properties, suggesting a common origin after the accretion of the parent body of Allende. Composition profiles at the rim/forsterite interfaces exhibit a plateau in the rim (typically Fa₄₅), a compositional jump of 10 Fa% at the interface, and a concentration gradient in the forsterite grain. Whatever the studied forsterite grain or whatever the nature of the interface, the Fe‐Mg profiles in forsterite grains have the same length of about 1.5 μm. This strongly suggests that the composition profiles were formed by solid‐state diffusion during the thermal metamorphism episode. Time–temperature couples associated with the diffusion process during thermal metamorphism are deduced from profile modeling. Considering the uncertainties on the diffusion coefficient value, we found that the peak temperature in Allende is ranging from 425 to 505 °C.     

A review of the chondrite–achondrite transition,and a metamorphic facies series for equilibrated primitive stony meteorites

Here, the petrological features of numerous primitive achondrites and highly equilibrated chondrites are evaluated to review and expand upon our knowledge of the chondrite–achondrite transition, and primitive achondrites in general. A thermodynamic model for the initial silicate melting temperature and progressive melting for nearly the entire known range of oxidation states is provided, which can be expressed as T_m = 0.035Fa²?3.51Fa + 1109 (in °C, where Fa is the proportion of fayalite in olivine). This model is then used to frame a discussion of textural and mineralogical evolution of stony meteorites with increasing temperature. We suggest that the metamorphic petrology of these meteorites should be based on diffusive equilibration among the silicate minerals, and as such, the chondrite–achondrite transition should be defined by the initial point of silicate melting, not by metal–troilite melting. Evidence of silicate melting is preserved by a distinctive texture of interconnected interstitial plagioclase ± pyroxene networks among rounded olivine and/or pyroxene (depending on ?O₂), which pseudomorph the former silicate melt network. Indirectly, the presence of exsolution lamellae in augite in slowly cooled achondrites also implies that silicate melting occurred because of the high temperatures required, and because silicate melt enhances diffusion. A metamorphic facies series is defined: the Plagioclase Facies is equivalent to petrologic types 5 and 6, the Sub‐calcic Augite Facies is bounded at lower temperatures by the initiation of silicate melting and at higher temperatures by the appearance of pigeonite, which marks the transition to the Pigeonite Facies.     

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.     

Mineralogy and petrography of amoeboid olivine aggregates from the reduced CV3 chondrites Efremovka,Leoville and Vigarano: Products of nebular condensation,accretion and annealing

Abstract— Amoeboid olivine aggregates (AOAs) from the reduced CV chondrites Efremovka, Leoville and Vigarano are irregularly‐shaped objects, up to 5 mm in size, composed of forsteritic olivine (Fa_<10) and a refractory, Ca, Al‐rich component. The AOAs are depleted in moderately volatile elements (Mn, Cr, Na, K), Fe, Ni‐metal and sulfides and contain no low‐Ca pyroxene. The refractory component consists of fine‐grained calcium‐aluminum‐rich inclusions (CAIs) composed of Al‐diopside, anorthite (An₁₀₀), and magnesium‐rich spinel (～1 wt% FeO) or fine‐grained intergrowths of these minerals; secondary nepheline and sodalite are very minor. This indicates that AOAs from the reduced CV chondrites are more pristine than those from the oxidized CV chondrites Allende and Mokoia. Although AOAs from the reduced CV chondrites show evidence for high‐temperature nebular annealing (e.g., forsterite grain boundaries form 120° triple junctions) and possibly a minor degree of melting of Al‐diopside‐anorthite materials, none of the AOAs studied appear to have experienced extensive (>50%) melting. We infer that AOAs are aggregates of high‐temperature nebular condensates, which formed in CAI‐forming regions, and that they were absent from chondrule‐forming regions at the time of chondrule formation. The absence of low‐Ca pyroxene and depletion in moderately volatile elements (Mn, Cr, Na, K) suggest that AOAs were either removed from CAI‐forming regions prior to condensation of these elements and low‐Ca pyroxene or gas‐solid condensation of low‐Ca‐pyroxene was kinetically inhibited.     

Northwest Africa 428: Impact‐induced annealing of an L6 chondrite breccia

Abstract— Northwest Africa (NWA) 428 is an L chondrite that was successively thermally metamorphosed to petrologic type‐6, shocked to stage S4–S5, brecciated, and annealed to approximately petrologic type‐4. Its thermal and shock history resembles that of the previously studied LL6 chondrite, Miller Range (MIL) 99301, which formed on a different asteroid. The petrologic type‐6 classification of NWA 428 is based on its highly recrystallized texture, coarse metal (150 ± 150 μm), troilite (100 ± 170 μm), and plagioclase (20–60 μm) grains, and relatively homogeneous olivine (Fa_{24.4 ± 0.6}), low‐Ca pyroxene (Fs_{20.5 ± 0.4}), and plagioclase (Ab_{84.2 ± 0.4}) compositions. The petrographic criteria that indicate shock stage S4–S5 include the presence of chromite veinlets, chromite‐plagioclase assemblages, numerous occurrences of metallic Cu, irregular troilite grains within metallic Fe‐Ni, polycrystalline troilite, duplex plessite, metal and troilite veins, large troilite nodules, and low‐Ca clinopyroxene with polysynthetic twins. If the rock had been shocked before thermal metamorphism, low‐Ca clinopyroxene produced by the shock event would have transformed into orthopyroxene. Post‐shock brecciation is indicated by the presence of recrystallized clasts and highly shocked clasts that form sharp boundaries with the host. Post‐shock annealing is indicated by the sharp optical extinction of the olivine grains; during annealing, the damaged olivine crystal lattices healed. If temperatures exceeded those approximating petrologic type‐4 (?600–700°C) during annealing, the low‐Ca clinopyroxene would have transformed into orthopyroxene. The other shock indicators, likewise, survived the mild annealing. An impact event is the most plausible source of post‐metamorphic, post‐shock annealing because any ²⁶Al that may have been present when the asteroid accreted would have decayed away by the time NWA 428 was annealed. The similar inferred histories of NWA 428 (L6) and MIL 99301 (LL6) indicate that impact heating affected more than 1 ordinary chondrite parent body.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

A relict‐grain‐bearing porphyritic olivine compound chondrule from LL3.0 Semarkona that experienced limited remelting

Abstract— Chondrule D8n in LL3.0 Semarkona is a porphyritic olivine (PO) chondrule, 1300 times 1900 μm in size, with a complicated thermal history. The oldest recognizable portion of D8n is a moderately high‐FeO, PO chondrule that is modeled as having become enmeshed in a dust ball containing a small, intact, low‐FeO porphyritic chondrule and fine‐grained material consisting of forsterite, kamacite, troilite, and possibly reduced C. The final chondrule melting event may have been a heat pulse that preferentially melted the low‐FeO material and produced a low‐FeO, opaque‐rich, exterior region, 45–140 μm in thickness, around the original chondrule. At one end of the exterior region, a kamacite‐ and troilite‐rich lump 960 μm in length formed. During the final melting event, the coarse, moderately ferroan olivine phenocrysts within the original chondrule appear to have been partly resorbed (These relict phenocrysts have the highest concentrations of FeO, MnO, and Cr₂O₃—7.5, 0.20, and 0.61 wt%, respectively—in D8n.). Narrow olivine overgrowths crystallized around the phenocrysts following final chondrule melting; their compositions seem to reflect mixing between melt derived from the exterior region and the resorbed margins of the phenocrysts. During the melting event, FeO in the relict phenocrysts was reduced, producing numerous small blebs of Ni‐poor metallic Fe along preexisting curvilinear fractures. The reduced olivine flanking the trails of metal blebs has lower FeO than the phenocrysts but virtually identical MnO and Cr₂O₃ contents. Subsequent parent‐body aqueous alteration in the exterior region of the chondrule formed pentlandite and abundant magnetite.     

The onset of metamorphism in ordinary and carbonaceous chondrites

Abstract— Ordinary and carbonaceous chondrites of the lowest petrologic types were surveyed by X‐ray mapping techniques. A variety of metamorphic effects were noted and subjected to detailed analysis using electron microprobe, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and cathodoluminescence (CL) methods. The distribution of Cr in FeO‐rich olivine systematically changes as metamorphism increases between type 3.0 and type 3.2. Igneous zoning patterns are replaced by complex ones and Cr‐rich coatings develop on all grains. Cr distributions in olivine are controlled by the exsolution of a Cr‐rich phase, probably chromite. Cr in olivine may have been partly present as tetrahedrally coordinated Cr³⁺. Separation of chromite is nearly complete by petrologic type 3.2. The abundance of chondrules showing an inhomogeneous distribution of alkalis in mesostasis also increases with petrologic type. TEM shows this to be the result of crystallization of albite. Residual glass compositions systematically change during metamorphism, becoming increasingly rich in K. Glass in type I chondrules also gains alkalis during metamorphism. Both types of chondrules were open to an exchange of alkalis with opaque matrix and other chondrules. The matrix in the least metamorphosed chondrites is rich in S and Na. The S is lost from the matrix at the earliest stages of metamorphism due to coalescence of minute grains. Progressive heating also results in the loss of sulfides from chondrule rims and increases sulfide abundances in coarse matrix assemblages as well as inside chondrules. Alkalis initially leave the matrix and enter chondrules during early metamorphism. Feldspar subsequently nucleates in the matrix and Na re‐enters from chondrules. These metamorphic trends can be used to refine classification schemes for chondrites. Cr distributions in olivine are a highly effective tool for assigning petrologic types to the most primitive meteorites and can be used to subdivide types 3.0 and 3.1 into types 3.00 through 3.15. On this basis, the most primitive ordinary chondrite known is Semarkona, although even this meteorite has experienced a small amount of metamorphism. Allan Hills (ALH) A77307 is the least metamorphosed CO chondrite and shares many properties with the ungrouped carbonaceous chondrite Acfer 094. Analytical problems are significant for glasses in type II chondrules, as Na is easily lost during microprobe analysis. As a result, existing schemes for chondrule classification that are based on the alkali content of glasses need to be revised.