CALCIUM-ALUMINIUM-RICH CHONDRULES IN THE UNEQUILIBRATED ORDINARY CHONDRITES

Calcium-aluminium-rich chondrules were found in L-3 (ALH-77015) and LL-3 (ALH-77278) chondrites. They consist of spinel, olivine, fassaite and glassy groundmass enriched in anorthite component. The bulk chemical compositions of the two chondrules are nearly the same and resemble those of the calcium-aluminium-rich inclusions in the carbonaceous chondrites, but the former is more enriched in MgO and SiO₂ and depleted in Al₂O₃ and CaO. The calcium-aluminium-rich chondrules would have been primarily early condensates which existed at the place where the chondrules were formed, and heated up to 1400 °C or higher to have melted and cooled at the rate similar to those for other chondrules, or the products of intensive heating followed by reaction with gas.     

A condensation model for the formation of chondrules in enstatite chondrites

Abstract— It is proposed that the chondrules in enstatite chondrites formed near the Sun from rain‐like supercooled liquid silicate droplets and condensed Fe‐Ni alloys in thermodynamic equilibrium with a slowly cooling nebula. FeO formed and dissolved in the droplets in an initial stage when the nucleation of iron was blocked, and was later mostly reduced to unalloyed Fe. At high temperatures, the silicate droplets contained high concentrations of the less volatile components CaO and Al₂O₃. At somewhat lower temperatures the equilibrium MgO content of the droplets was relatively high. As cooling progressed, some droplets gravitated toward the Sun, and moved in other directions, depleting the region in CaO, Al₂O₃, and MgO and accounting for the relatively low observed CaO/SiO₂, Al₂O₃/SiO₂, and MgO/SiO₂ ratios in enstatite chondrites. At approximately 1400 K, the remaining supercooled silicate droplets crystallized to form MgSiO₃ (enstatite) with small amounts of olivine and a high‐SiO₂ liquid phase which became the mesostases. The high enstatite content is the result of the supercooled chondrules crystallizing at a relatively low temperature and relatively high total pressure. Finally, FeS formed at temperatures below 680 K by reaction of the condensed Fe with H₂S. All calculations were performed with the evaluated optimized thermodynamic databases of the FactSage thermodynamic computer system. The thermodynamic properties of compounds and solutions in these databases were optimized completely independently of any meteoritic data. Agreement of the model with observed bulk and phase compositions of enstatite chondrules is very good and is generally within experimental error limits for all components and phases.     

Reclassification of Hart and Northwest Africa 6047: Criteria for distinguishing between CV and CK3 chondrites

The single parent body model for the CV and CK chondrites (Greenwood et al. 2010 ) was challenged by Dunn et al. ( 2016a ), who argued that magnetite compositions could not be reconciled by a single metamorphic sequence (i.e., CV3 → CK3 → CK4–6). Cr isotopic compositions, which are distinguishable between the CV and CK chondrites, also support two different parent bodies (Yin et al. 2017 ). Despite this, there are many petrographic and mineralogical similarities between the unequilibrated (petrologic type 3) CK chondrites and the CV chondrites (also type 3), which may result in misclassification of samples. Hart and Northwest Africa 6047 (NWA 6047) are an excellent example of this. In this study, we revisit the classification of Hart and NWA 6047 using magnetite compositions, petrography, and compositions of olivine, the most ubiquitous mineral in both CV and CK chondrites. Not only do our results suggest that NWA 6047 and Hart were misclassified, but our assessment of CV and CK3 chondrites has also led to the development of criteria that can be used to distinguish between CV and CK3 chondrites. These criteria include: abundances of Cr₂O₃, TiO₂, NiO, and Al₂O₃ in magnetite; Fa content and NiO abundance of matrix olivine; FeO content of chondrules; and the chondrule:matrix ratio. Classification as a CV chondrite is also supported by the presence of igneous chondrule rims, calcium‐aluminum‐rich inclusions, and an elongated petrofabric. However, none of these petrographic characteristics can be used conclusively to distinguish between CV and CK3 chondrites.     

AN H4–6 CHONDRITE: MOTTA DI CONTI

The mineralogical and chemical compositions of meteorites from the Motta di Conti, Vercelli, Italy, shower (February 29, 1868) have been determined. Microprobe analyses, of olivine (Fa_19,6) and orthopyroxene (Fs_17,8), as well as the bulk chemical composition, particularly the ratios of SiO₂/MgO (1.50), Fe°/Ni° (11.03), Fe_total/SiO₂ (0.81), Fe°/Fe_total (0.70) and the content of Fe_total (28.60%) classify the meteorite as an H-group chondrite. The percentage of total metallic nickel-iron (22.06%) is somewhat higher than the average in H-group chondrites. The texture of our stone shows evidence of metamorphism. The integration between matrix and chondrules is advanced and may suggest a high petrographic grade, but the identification of several microscopic features (e.g. small grains of monoclinic twinned pyroxene, FeNi-FeS intergrowths, globules and mosaic) leads to the conclusion that a variety of petrographic types (4–6) are present. Metamorphic equilibration in chondrites is discussed and a preliminary hypothesis for H4–6 chondrites is suggested.     

Petrographic classification of Middle Ordovician fossil meteorites from Sweden

Abstract— The maximum diameter of chromite (FeCr₂O₄) grains within L chondrites reflects the petrographic type of the sample. On the basis of our measurements of nine recent L chondrites, L3 chromite D_max = 34–50 μm, L4 = 87–150 μm, L5 = 76–158 μm, and L6 = 253–638 μm. This variation reflects the crystallization of the chromite grains during parent body thermal metamorphism. We use this calibration to classify six fossil meteorites from the Middle Ordovician in Sweden as type 3 (or 4) to 6. The high flux of L chondrites at 470 Ma contained a range of petrographic types and may have had a higher proportion of lower petrographic type meteorites than are found in recent L chondrite falls. The fossil meteorites have in places preserved recognizable chondrule textures, including porphyritic olivine, barred olivine, and radiating pyroxene. A large relict clast and fusion crust have also been tentatively identified in one fossil meteorite. Apart from chromite, all of the original meteorite minerals have been replaced by carbonate (and sheet silicate and sulfate) during diagenesis within the limestone host. The preservation of chondrule definition has allowed us to measure the mean diameters of relict chondrules. The range (0.4–0.6 mm) is consistent with measurements made in the same way on recent L chondrites.     

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 (Fs_0.6–8.8Wo_0.7–9.3) has much higher Al₂O₃ and TiO₂ contents (up to 12.5 and 2.3 wt%, respectively) than that in ferromagnesian chondrules. High‐Ca pyroxene (Fs_0.3–2.0Wo_33–54) contains less Al₂O₃ and TiO₂ than that in Ca,Al‐rich inclusions (CAIs). Plagioclase (An_77–99Ab_1–23) 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.     

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.     

40Ar-39Ar Ages of Types 3 and 4, L and H Chondrites from Antarctica

Abstract— This is a report on ⁴⁰Ar-³⁹Ar studies of 7 low petrographic type L and H chondrites from Antarctica. From petrographic similarities it has been argued that the L3 chondrites ALHA77015, ?77167, ?77249, and ?77260 are pieces from a common fall (McKinley et al., 1981). Our results now confirm this supposition: The four meteorites have identical characteristic Ar-degassing patterns, very similar K, Ca, Cl, and ³⁶Ar_trapped contents, and similar ⁴⁰Ar-³⁹Ar ages of <4 Ga which are rather unusual for ordinary chondrites and might be due to shock. The undulating age patterns could be due to weathering or to ³⁹Ar recoil. The L4 chondrite ALHA77230 shows no age plateau and only a lower limit for the time of a severe degassing, 4.0 Ga, can be given. ALHA77226 and RKPA78002, two H4 chondrites, exhibit reasonably well defined age plateaus at about 4.3 and 4.4 Ga. Two individual chondrules from RKPA78002 have the same age as the whole rock sample.     

A petrogenetic model for the origin and compositional variation of the martian basaltic meteorites

Abstract— The major element, trace element, and isotopic compositional ranges of the martian basaltic meteorite source regions have been modeled assuming that planetary differentiation resulted from crystallization of a magma ocean. The models are based on low to high pressure phase relationships estimated from experimental runs and estimates of the composition of silicate Mars from the literature. These models attempt to constrain the mechanisms by which the martian meteorites obtained their superchondritic CaO/Al₂O₃ ratios and their source regions obtained their parent/daughter (⁸⁷Rb/⁸⁶Sr, ¹⁴⁷Sm/¹⁴⁴Nd, and ¹⁷⁶Lu/¹⁷⁷Hf) ratios calculated from the initial Sr, Nd, and Hf isotopic compositions of the meteorites. High pressure experiments suggest that majoritic garnet is the liquidus phase for Mars relevant compositions at or above 12 GPa. Early crystallization of this phase from a martian magma ocean yields a liquid characterized by an elevated CaO/Al₂O₃ ratio and a high Mg#. Olivine‐pyroxene‐garnet‐dominated cumulates that crystallize subsequently will also be characterized by superchondritic CaO/Al₂O₃ ratios. Melting of these cumulates yields liquids with major element compositions that are similar to calculated parental melts of the martian meteorites. Furthermore, crystallization models demonstrate that some of these cumulates have parent/daughter ratios that are similar to those calculated for the most incompatible‐element‐depleted source region (i.e., that of the meteorite Queen Alexandra [QUE] 94201). The incompatible‐element abundances of the most depleted (QUE 94201‐like) source region have also been calculated and provide an estimate of the composition of depleted martian mantle. The incompatible‐element pattern of depleted martian mantle calculated here is very similar to the pattern estimated for depleted Earth's mantle. Melting the depleted martian mantle composition reproduces the abundances of many incompatible elements in the parental melt of QUE 94201 (e.g., Ba, Th, K, P, Hf, Zr, and heavy rare earth elements) fairly well but does not reproduce the abundances of Rb, U, Ta and light rare earth elements. The source regions for meteorites such as Shergotty are successfully modeled as mixtures of depleted martian mantle and a late stage liquid trapped in the magma ocean cumulate pile. Melting of this hybrid source yields liquids with major element abundances and incompatible‐element patterns that are very similar to the Shergotty bulk rock.     

Nonporphyritic chondrules and chondrule fragments in enstatite chondrites: Insights into their origin and secondary processing

Sixteen nonporphyritic chondrules and chondrule fragments were studied in polished thin and thick sections in two enstatite chondrites (ECs): twelve objects from unequilibrated EH3 Sahara 97158 and four objects from equilibrated EH4 Indarch. Bulk major element analyses, obtained with electron microprobe analysis (EMPA) and analytical scanning electron microscopy (ASEM), as well as bulk lithophile trace element analyses, determined by laser ablation inductively coupled plasma–mass spectrometry (LA‐ICP‐MS), show that volatile components (K₂O + Na₂O versus Al₂O₃) scatter roughly around the CI line, indicating equilibration with the chondritic reservoir. All lithophile trace element abundances in the chondrules from Sahara 97158 and Indarch are within the range of previous analyses of nonporphyritic chondrules in unequilibrated ordinary chondrites (UOCs). The unfractionated (solar‐like) Yb/Ce ratio of the studied objects and the mostly unfractionated refractory lithophile trace element (RLTE) abundance patterns indicate an origin by direct condensation. However, the objects possess subchondritic CaO/Al₂O₃ ratios; superchondritic (Sahara 97158) and subchondritic (Indarch) Yb/Sc ratios; and chondritic‐normalized deficits in Nb, Ti, V, and Mn relative to RLTEs. This suggests a unique nebular process for the origin of these ECs, involving elemental fractionation of the solar gas by the removal of oldhamite, niningerite, and/or another phase prior to chondrule condensation. A layered chondrule in Sahara 97158 is strongly depleted in Nb in the core compared to the rim, suggesting that the solar gas was heterogeneous on the time scales of chondrule formation. Late stage metasomatic events produced the compositional diversity of the studied objects by addition of moderately volatile and volatile elements. In the equilibrated Indarch chondrules, this late process has been further disturbed, possibly by a postaccretional process (diffusion?) that preferentially mobilized Rb with respect to Cs in the studied objects.     

Chemistry and oxygen isotopic composition of cluster chondrite clasts and their components in LL3 chondrites

Cluster chondrites are characterized by close‐fit textures of deformed and indented chondrules, taken as evidence for hot chondrule accretion (Metzler 2012 ). We investigated seven cluster chondrite clasts from six brecciated LL3 chondrites and measured their bulk oxygen isotopic and chemical composition, including REE, Zr, and Hf. The same parameters were measured in situ on 93 chondrules and 4 interchondrule matrix areas. The CI‐normalized REE patterns of the clasts are flat, showing LL‐chondritic concentrations. The mean chemical compositions of chondrules in clasts and other LL chondrites are indistinguishable and we conclude that cluster chondrite chondrules are representative of the normal LL chondrule population. Type II chondrules are depleted in MgO, Al₂O₃ and refractory lithophiles (REE, Zr, Hf) by factors between 0.65 and 0.79 compared to type I chondrules. The chondrule REE patterns are basically flat with slight LREE < HREE fractionations. Many chondrules exhibit negative Eu anomalies while matrix shows a complementary pattern. Chondrules scatter along a correlation line with a slope of 0.63 in the oxygen 3‐isotope diagram, interpreted as the result of O‐isotope exchange between chondrule melts and ¹⁸O‐rich nebular components. In one clast, a distinct anticorrelation between chondrule size and δ¹⁸O is found, which may indicate a more intense oxygen isotope exchange by smaller chondrules. In some clasts the δ¹⁸O values of type I chondrules are correlated with concentrations of SiO₂ and MnO and anticorrelated with MgO, possibly due to the admixture of a SiO₂‐ and MnO‐rich component to chondrule melts during oxygen isotope exchange. Two chondrules with negative anomalies in Sm, Eu, and Yb were found and may relate their precursors to refractory material known from group III CAIs. Furthermore, three chondrules with strong LREE > HREE and Zr/Hf fractionations were detected, whose formation history remains to be explained.     

Perceptive of the pyroxene-bearing micrometeorites and their relation to chondrites

We studied 149 pyroxenes from 69 pyroxene-bearing micrometeorites collected from deep-sea sediments of the Indian Ocean and South Pole Water Well at Antarctica, Amundsen-Scott South Pole station. The minor elements in pyroxenes from micrometeorites are present in the ranges as follows: MnO ~0.0–0.4 wt%, Al₂O₃ ~0.0–1.5 wt%, CaO ~0.0–1.0 wt%, Cr₂O₃ ~0.3–0.9 wt%, and FeO ~0.5–4 wt%. Their chemical compositions suggest that pyroxene-bearing micrometeorites are mostly related to precursors from carbonaceous chondrites rather than ordinary chondrites. The Fe/(Fe+Mg) ratio of the pyroxenes and olivines in micrometeorites shows similarities to carbonaceous chondrites with values lying between 0 and 0.2, and those with values beyond this range are dominated by ordinary chondrites. Atmospheric entry of the pyroxene-bearing micrometeorites is expected to have a relatively low entry velocity of <16 km s⁻¹ and high zenith angle (70–90°) to preserve their chemical compositions. In addition, similarities in the pyroxene and olivine mineralogical compositions between carbonaceous chondrites and cometary particles suggest that dust in the solar system is populated by materials from different sources that are chemically similar to each other. Our results on pyroxene chemical compositions reveal significant differences with those from ordinary chondrites. The narrow range in olivine and pyroxene chemical compositions are similar to those from carbonaceous chondrites, and a small proportion to ordinary chondrites indicates that dust is largely sourced from carbonaceous chondrite-type bodies.     

Experimental constraints on alkali condensation in chondrule formation

Abstract— To assess whether the alkali behavior observed in chondrules of primitive meteorites is attributable to volatilization from the raw materials of chondrules during chondrule formation events or attributable to condensation processes from the nebular gas, we set up a new experimental device able to expose silicate melt samples to a controlled alkali partial pressure at high temperature under fixed O fugacity. Using a mixture of potassium carbonate (K₂CO₃) and graphite (C) as the source of the K gas (K_g), we studied the condensation kinetics of K and its solubility in CaO‐MgO‐Al₂O₃‐SiO₂ silicate melts, according to the reaction 2 K _(g) + 1/2 _(g) = K₂O _(melt) From these results, we show that alkali entering in chondrules from the nebular gas is a viable mechanism to explain the chondrules alkali contents and their δ⁴¹K‐isotopic signatures, at timescales relevant to chondrule formation. Finally, we also suggest that chondrules may have formed in non‐canonical nebular environments and that the flash‐heating scenario is not a prerequisite to chondrule formation.     

Oxygen isotope and 26Al‐26Mg systematics of aluminum‐rich chondrules from unequilibrated enstatite chondrites

Abstract— Correlated in situ analyses of the oxygen and magnesium isotopic compositions of aluminum‐rich chondrules from unequilibrated enstatite chondrites were obtained using an ion microprobe. Among eleven aluminum‐rich chondrules and two plagioclase fragments measured for ²⁶Al‐²⁶Mg systematics, only one aluminum‐rich chondrule contains excess ²⁶Mg from the in situ decay of ²⁶Al; the inferred initial ratio (²⁶Al/²⁷Al)_o = (6.8 ± 2.4) × 10^?6 is consistent with ratios observed in chondrules from carbonaceous chondrites and unequilibrated ordinary chondrites. The oxygen isotopic compositions of five aluminum‐rich chondrules and one plagioclase fragment define a line of slope ?0.6 ± 0.1 on a three‐oxygen‐isotope diagram, overlapping the field defined by ferromagnesian chondrules in enstatite chondrites but extending to more ¹⁶O‐rich compositions with a range in δ¹⁸O of about ?12‰. Based on their oxygen isotopic compositions, aluminum‐rich chondrules in unequilibrated enstatite chondrites are probably genetically related to ferromagnesian chondrules and are not simple mixtures of materials from ferromagnesian chondrules and calcium‐aluminum‐rich inclusions (CAIs). Relative to their counterparts from unequilibrated ordinary chondrites, aluminum‐rich chondrules from unequilibrated enstatite chondrites show a narrower oxygen isotopic range and much less resolvable excess ²⁶Mg from the in situ decay of ²⁶Al, probably resulting from higher degrees of equilibration and isotopic exchange during post‐crystallization metamorphism. However, the presence of ²⁶Al‐bearing chondrules within the primitive ordinary, carbonaceous, and now enstatite chondrites suggests that ²⁶Al was at least approximately homogeneously distributed across the chondrite‐forming region.     

SIZE FREQUENCY DISTRIBUTIONS OF FLUID DROP CHONDRULES IN ORDINARY CHONDRITES

The size frequency distributions of fluid drop chondrules in 11 ordinary chondrites (five H3, one H4, four L3, one LL3) have been determined by optical measurements in petrographic thin sections. The extreme range of median size of the fluid drop chondrules in individual meteorites is only slightly greater than lφ unit, and the grain size frequency distributions are approximately log normal. Chondrule size frequency distributions generally are fine skewed, platykurtic, and indicate moderate sorting. The size frequency distributions of fluid drop chondrules in ordinary chondrites are distinctly coarser than similar chondrules measured previously in CM2 and C03 carbonaceous chondrites.     

The Bencubbin chondrite breccia and its relationship to CR chondrites and the ALH85085 chondrite

Abstract— Bencubbin is an unclassified meteorite breccia which consists mainly of host silicate (～40 vol.%) and host metal (～60%) components. Rare (< 1%) ordinary chondrite clasts and a dark xenolith (formerly called a carbonaceous chondrite clast) are also found. A petrologic study of the host silicates shows that they have textures, modes, mineralogy and bulk compositions that are essentially the same as that of barred olivine (BO) chondrules, and they are considered to be BO chondritic material. Bulk compositions of individual host silicate clasts are identical and differ only in their textures which are a continuum from coarsely barred, to finely barred, to feathery microcrystalline; these result from differing cooling rates. The host silicates differ from average BO chondrules only in being angular clasts rather than fluid droplet-shaped objects, and in being larger in size (up to 1 cm) than most chondrules; but large angular to droplet-shaped chondrules occur in many chondrites. Bencubbin host metallic FeNi clasts have a positive Ni-Co trend, which coincides with that of a calculated equilibrium nebular condensation path. This appears to indicate a chondritic, rather than impact, origin for this component as well. The rare ordinary chondrite clast and dark xenolith also contain FeNi metal with compositions similar to that of the host metal. Two scenarios are offered for the origin of the Bencubbin breccia. One is that the Bencubbin components are chondritic and were produced in the solar nebula. Later brecciation, reaggregation and minor melting of the chondritic material resulted in it becoming a monomict chondritic breccia. The alternative scenario is that the Bencubbin components formed as a result of major impact melting on a chondritic parent body; the silicate fragments were formed from an impact-induced lava flow and are analogous to the spinifex-textured rocks characteristic of terrestrial komatiites. Both scenarios have difficulties, but the petrologic, chemical and isotopic data are more consistent with Bencubbin being a brecciated chondrite. Bencubbin has a number of important chemical and isotopic characteristics in common with the major components in the CR (Renazzo-type) chondrites and the unique ALH85085 chondrite, which suggests that their major components may be related. These include: (1) Mafic silicates that are similarly Mg-rich and formed in similar reducing environments. (2) Similarly low volatiles; TiO₂, Al₂O₃ and Cr₂O₃ contents are also similar. (3) Similar metallic FeNi compositions that sharply differ from those in other chondrites. (4) Remarkable enrichments in ¹⁵N. (5) Similar oxygen isotopic compositions that lie on the same mixing line. Thus, the major components of the Bencubbin breccia are highly similar to those of the ALH85085 and CR chondrites and they may have all formed in the same isotopic reservoir, under similar conditions, in the CR region of the solar nebula.     

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.     

TWO NEW CHONDRITE-FALLS IN JAPAN

In the summer of 1984, two meteorites fell in the northern part of Honshu, Japan; Aomori, at 1:50 p.m. on June 30, and Tomiya, at 1:35 p.m. on August 22. Coordinates of the falls of the Aomori and the Tomiya are at 140°47.1'E., 40°48.6'N., and 140°51.9'E., 38°22.0'N., respectively. Results of chemical analyses of major elements, ratios of Fe_total/SiO₂ (0.546 and 0.803) and Fe_metal/Fe_total (0.332 and 0.581), and molar compositions of olivines (Fa₂₅ and Fa₁₉) indicate that the Aomori and the Tomiya are typical L- and H-group ordinary chondrites, respectively. In the Aomori, chondrules are present as relicts in the well-recrystallized matrix. Olivine and pyroxene are homogeneous in composition, and coarse clear feldspar, up to 100 micrometers in size, is well developed in the chondrules and matrix. Though the Aomori is a petrologic type 6 based on its texture and mineralogy, it includes a few grains of multiple twinned clinobronzite which is rarely observed in highly equilibrated ordinary chondrites. In the Tomiya, chondrules possess a fine-grained mesostasis, and both orthopyroxene and clinobronzite are noticeable in thin sections. Plagioclase is mostly microcrystalline, but is also sparsely present as tiny, visible grains. Thus, the Tomiya was classified to be petrologic type between 4 and 5. The deformation texture of olivine, pyroxene and plagioclase indicates that both meteorites were shocked by 0.2-0.25 Mb. In conjunction with the discussion of the frequency of meteorite-falls, all observed falls of meteorites in Japan are tabulated in this paper.     

THE CORREO AND SUWANEE SPRING METEORITES: TWO NEW ORDINARY CHONDRITE FINDS

Two new ordinary chondrites were found about 40 km west of Albuquerque, New Mexico. Correo is an H4 chondrite with distinct chondrules and major olivine (Fo_81.4), orthopyroxene (En_82.3) and plagioclase (An₁₂). Suwanee Spring is an L5 chondrite with few distinct chondrules and a highly recrystallized matrix. Major minerals are olivine (Fo_75.4), orthopyroxene (En_77.7) and plagioclase (An₉). The metallic Ni-Fe phases of both meteorites are typical of slowly-cooled ordinary chondrites.     

Petrology and Raman spectroscopy of high pressure phases in the Gujba CB chondrite and the shock history of the CB parent body

Abstract– High pressure phases majorite, possibly majorite‐pyrope_ss, wadsleyite, and coesite are present in the matrix and in barred olivine fragments in the Gujba CB chondrite. Grossular‐pyrope was also observed in some small inclusions. The CB chondrites are metal‐rich meteorites with characteristics that sharply distinguish them from other chondrite groups. All of the CB chondrites contain impact melt regions interstitial to their chondrules, fragments and metal and a major impact event (or events), on the CB chondrite parent body is clearly a significant stage in its history. We studied three areas interstitial to chondrules and metal in the Gujba CB_a chondrite. From Raman spectra, the barred olivine fragments and matrix in these regions have various combinations of olivine and low‐Ca pyroxene, as well as majorite garnet (Mg₄Si₄O₁₂), a phase that forms by high‐pressure transformation of low‐Ca pyroxene and wadsleyite, a high pressure product of olivine. Compositions of the majorite suggest both majorite and majorite‐pyrope solid solution may be present. The mineral assemblage of majorite and wadsleyite suggest minimum shock pressures and temperatures of ～19 GPa and ～2000 °C, respectively. The occurrences of high pressure phases are variable from one area to another, on the scale of millimeters or less, suggesting heterogeneous distribution of shock and/or back transformation to low pressure polymorphs throughout the meteorite. The high pressure phases record a high temperature–pressure impact event that is superimposed onto, and thus postdates formation of, the chondrules and other components in the CB chondrites. The barred chondrules and metal in the CB chondrites are primary materials formed prior to the impact event either generated in an earlier planetesimal scale impact event or in the nebula.