THE COMPOSITION OF THE JOHNSTOWN METEORITE

A new analysis of the Johnstown meteorite, a hypersthene achondrite, gives the following results (weight percent): SiO₂ 53.48, TiO₂ 0.12, Al₂O₃ 1.43, Cr₂O₃ 0.83, FeO 15.63, MnO 0.54, MgO 25.87, CaO 1.40, Na₂O 0.04, K₂O 0.00, P₂O₅ 0.00, H₂O+ <0.1, H₂O- 0.05, Ni <0.05, Co <0.01, FeS 1.18, sum 100.57. Published and unpublished data on minor and trace elements in the bulk meteorite and in the pyroxene are presented in tabular form.     

Spinels and oxygen fugacity in olivine‐phyric and lherzolitic shergottites

Abstract— We examine the occurrences, textures, and compositional patterns of spinels in the olivine‐phyric shergottites Sayh al Uhaymir (SaU) 005, lithology A of Elephant Moraine A79001 (EET‐A), Dhofar 019, and Northwest Africa (NWA) 1110, as well as the Iherzolitic shergottite Allan Hills (ALH) A77005, in order to identify spinel‐olivine‐pyroxene assemblages for the determination of oxygen fugacity (using the oxybarometer of Wood [1991]) at several stages of crystallization. In all of these basaltic martian rocks, chromite was the earliest phase and crystallized along a trend of strict Cr‐Al variation. Spinel (chromite) crystallization was terminated by the appearance of pyroxene but resumed later with the appearance of ulvöspinel. Ulvöspinel formed overgrowths on early chromites (except those shielded as inclusions in olivine or pyroxene), retaining the evidence of the spinel stability gap in the form of a sharp core/rim boundary (except in ALH A77005, where subsolidus reequilibration diffused this boundary). Secondary effects seen in chromites include reaction with melt before ulvöspinel overgrowth, reaction with melt inclusions, reaction with olivine hosts (in ALH A77005), and exsolution of ulvöspinel or ilmenite. All chromites experienced subsolidus Fe/Mg reequilibration. Spinel‐olivine‐pyroxene assemblages representing the earliest stages of crystallization in each rock essentially consist of the highest‐Cr#, lowest‐fe# chromites not showing secondary effects plus the most magnesian olivine and equilibrium low‐Ca pyroxene. Assemblages representing the onset of ulvöspinel crystallization consist of the lowest‐Ti ulvöspinel, the most magnesian olivine in which ulvöspinel occurs as inclusions, and equilibrium low‐Ca pyroxene. The results show that, for early crystallization conditions, oxygen fugacity (fO₂) increases from SaU 005 and Dhofar 019 (?QFM ‐3.8), to EET‐A (QFM ‐2.8) and ALH A77005 (QFM ‐2.6), to NWA 1110 (QFM ‐1.7). Estimates for later conditions indicate that in SaU 005 and Dhofar 019 oxidation state did not change during crystallization. In EET‐A, there was an increase in fO₂ that may have been due to mixing of reduced material with a more oxidized magma. In NWA 1110, there was a dramatic increase, indicating a non‐buffered system, possibly related to its high oxidation state. Differences in fO₂ among shergottites are not primarily due to igneous fractionation but, rather, to derivation from (and possibly mixing of) different reservoirs.     

Petrology of unique achondrite Queen Alexandra Range 93148: A piece of the pallasite (howardite‐eucrite‐diogenite?) parent body?

Abstract— Queen Alexandra Range (QUE) 93148 is a small (1.1 g) olivine‐rich achondrite (mg 86) that contains variable amounts of orthopyroxene (mg 87) and kamacite (6.7 wt% Ni), with minor augite. Olivine in QUE 93148 contains an unusual suite of inclusions: (1) 5 × 100 μm sized lamellae with a CaO‐ and Cr₂O₃‐rich (～10 and 22 wt%, respectively) composition that may represent a submicrometer‐scale intergrowth of chromite and pyroxene(s); (2) 75 × 500 μm sized lamellar symplectites composed of chromite and two pyroxenes, with minor metal; (3) 15–20 μm sized, irregularly‐shaped symplectites composed of chromite and pyroxene(s); (4) 100–150 μm sized, elliptical inclusions composed of chromite, two pyroxenes, metal, troilite, and rare whitlockite. Type 1, 2, and 3 inclusions probably formed by exsolution from the host olivine during slow cooling, whereas type 4 more likely resulted from early entrapment of silicate and metallic melts followed by closed‐system oxidation. Queen Alexandra Range 93148 can be distinguished from most other olivine‐rich achondrites (ureilites, winonaites, lodranites, acapulcoites, brachinites, Eagle‐Station‐type pallasites, and pyroxene pallasites), as well as from mesosiderites, by some or all of the following properties: O‐isotopic composition, Fe‐Mn‐Mg relations of olivine, CaO and Cr₂O₃ contents of olivine, orthopyroxene compositions, molar Cr/(Cr + Al) ratios of chromite, metal composition, texture, and the presence of the inclusions. In terms of many of these properties, it shows an affinity to main‐group pallasites. Nevertheless, it cannot be identified as belonging to this group. Meteorite QUE 93148 appears to be a unique achondrite. Possibly it should be considered to be a pyroxene pallasite that is genetically related to main‐group pallasites. Alternatively, it may be derived from the mantle of the pallasite (howardite‐eucrite‐diogenite?) parent body.     

THE MINERALOGY AND CHEMISTRY OF THE ALTA'AMEEM METEORITE

The Alta'ameem hypersthene chondrite is a light gray brecciated and metamorphosed meteorite composed mainly of olivine (27% Fa), orthopyroxene (24.5% Fs) and plagioclase (An¹⁰). Other minerals include troilite, kamacite, taenite, chromite, ilmenite, clinopyroxene, chalcopyrite, and apatite or merrillite. The mineralogical and chemical analyses suggest that the Alta'ameem meteorite belongs to the amphoterite group of chondrites. The chemical composition includes the following: Fe 3.39, Ni 1.13, Co 0.05, Cu 0.01, FeS 6.48, SiO₂ 39.48, TiO₂ 0.28, Al₂O₃ 2.25, FeO 16.46, MnO 0.40, MgO 25.66, CaO 1.47, Na₂O 1.05, K₂O 0.15, P₂O₅ 0.47, Cr₂O₃ 0.45; total 99.18.     

CAMEL DONGA METEORITE,A NEW EUCRITE FROM THE NULLARBOR PLAIN,WESTERN AUSTRALIA

Twelve stones, ranging up to 504 g (total weight 2.92 kg), of a very fresh eucrite have been collected from a 1 km² area on the Nullarbor Plain in Western Australia. The location is approximately 75 km N6°E from Nurina Siding on the Trans-Australian Railway; coordinates 30°19′S, 126°37′E. This eucrite consists almost entirely of pyroxene (mean composition Wo 16 Fs 49) and plagioclase (mean composition An 85) in approximate proportions 3: 2, with 2% almost pure Fe metal and accessory amounts of troilite, ilmenite, and an SiO₂ phase. Gabbroic and doleritic clasts are present in a groundmass of comminuted pyroxene and plagioclase. The chemical composition (weight per cent) is: SiO₂ 49.53, TiO₂ 0.74, Al₂O₃ 12.49, Cr₂O₃ 0.33, FeO 16.07, MnO 0.56, MgO 6.31, CaO 10.41, Na₂O 0.49, K₂O 0.04, P₂O₅ < 0.01, H₂O + < 0.1, H₂O — 0.07, Fe metal 2.07, Ni < 0.01, Co < 0.01, FeS 0.19, C 0.03, sum 99.33.     

Complexly zoned chromium‐aluminum spinel found in situ in the Allende meteorite

Abstract— In addition to the Mg‐, Al‐, ¹⁶O‐rich spinels that are known to occur in refractory inclusions, the Murchison meteorite contains Cr‐rich, ¹⁶O‐poor spinels, most of whose sources are unknown because they are rarely found in situ. Here we report the in situ occurrence in Allende of Cr‐rich spinels, found in 13 chondrules and 4 “olivine‐rich objects”. The Allende spinels exhibit major and minor element contents, isotopic compositions, and zoning of Cr₂O₃ contents like those of the Cr‐spinels from Murchison. Some chondrules contain patchy‐zoned spinel (Simon et al., 1994), which suggests that such grains did not form by sintering but perhaps by formation of overgrowths on relic grains. Unlike the olivine‐rich objects, phases in all three chondrules that were analyzed by ion microprobe have uniform, near‐normal O‐isotopic compositions. One olivine‐rich object, ALSP1, has a huge (1 mm) fragment of chevron‐zoned spinel. This spinel has near‐normal O‐isotopic compositions that are quite distinct from those of adjacent forsteritic olivine, which are relatively ¹⁶O‐rich and plot on the calcium‐aluminum‐inclusion (CAI) line, like some isolated forsterite grains found in Allende. The spinel and olivine in this object are therefore not genetically related to each other. Another olivine‐rich object, ALSP11A, contains a rectangular, 150 ×s 100 μm, homogeneous spinel grain with 50 wt% Cr₂O₃ and 23 wt% FeO in a vuggy aggregate of finer‐grained (5–90 μm), FeO‐rich (Fo_47–55) olivine. The magnesian core of one olivine grain has a somewhat ¹⁶O‐rich isotopic composition like that of the large spinel, whereas the FeO‐rich olivine is relatively ¹⁶O‐poor. The composition of the spinel in ALSP11A plots on the CAI line, the first Cr‐rich spinel found to do so. Chevron‐zoned spinel has not been observed in chondrules, and it is unlikely that either ALSP1 or ALSP11A were ever molten. Calculations show that a spinel with the composition of that in ALSP1 can condense at 1780 K at a P^tot of 10^?3 atm and a dust/gas ratio of 100 relative to solar. The Cr‐rich spinel in ALSP11A could condense at ～1420 K, but this would require a dust/gas enrichment of 1000 relative to solar. The data presented here confirm that, as in Murchison, the coarse Cr‐rich spinels in Allende are relatively ¹⁶O‐depleted and are isotopically distinct from the ¹⁶O‐enriched MgAl₂O₄ from CAIs. Sample ALSP11A may represent a third population, one that is Cr‐rich and plots on the CAI line. That the O‐isotopic composition of ALSP1 is like those of Cr‐rich spinels from chondrules indicates that O‐isotopic compositions cannot be used to distinguish whether grains from such unequilibrated objects are condensates or are fragments from a previous generation of chondrules.     

MINERALOGY AND CHEMISTRY OF THE KYLE,TEXAS, CHONDRITE

The Kyle, Texas, U.S.A., chondrite was identified in 1965. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 26.2 mole %), orthopyroxene (Fs 21.0 mole %), clinopyroxene, plagioclase (An 10.3 mole %), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. Eutectic intergrowths of metaltroilite and a brecciated matrix indicate that the Kyle chondrite was shocked. Recrystallization and shock have obliterated chondrule-matrix boundaries. A chemical analysis of the meteorite shows the following results (in weight %): Fe 0.38, Ni 1.22, Co 0.05, FeS 5.98, SiO₂ 38.41, TiO₂ 0.11, Al₂O₃ 2.13, Cr₂O₃ 0.55, Fe₂O₃ 8.02, FeO 14.83, MnO 0.31, MgO 23.10, CaO 1.60, Na₂O 0.74, K₂O 0.08, P₂O₅ 0.19, H₂O⁺ 1.73, H₂O^? 0.37, C 0.03, Sum 99.83. On the basis of bulk chemistry, composition of olivine and orthopyroxene, and the recrystallized matrix, the Kyle meteorite is classified as an L6 chondrite.     

NIOBIAN RUTILE IN AN APOLLO 14 KREEP FRAGMENT

Niobian rutile was found in a KREEP lithic fragment of basaltic texture. The niobian rutile contains 85.3% TiO₂, 7.1% Nb₂O₅, 2.65% Cr₂O₃, 0.70% ZrO₂, 0.61% SiO₂, 0.82% Al₂O₃ 0.61% FeO, 0.52% CaO, 0.22% V₂O₃ in addition to minor amounts of MnO, MgO, and CeO₂. Rare earth elements were not detected, in contrast with lunar niobian rutile of Marvin (1971). Coexisting minerals in the KREEP fragment are major amounts of plagioclase and orthopyroxene, and minor amounts of olivine, ilmenite, augite, barian K-feldspar, whitlockite, troilite, Ni-Fe, zirkelite and chromite     

THE CHEMISTRY AND MINERALOGY OF THE HOMEWOOD,MANITOBA, METEORITE

The Homewood meteorite is a slightly weathered find of 325 grams discovered in 1970 about 64 km southwest of Winnipeg, Manitoba. It consists of olivine (Fa_25.4; 43.8 normative wt. percent), orthopyroxene (Fs_23.3; 28.5 percent), kamacite and taenite (7.5 percent), troilite (5.6 percent), maskelynite (8.3 percent), chromite (1.0 percent), whitlockite (0.7 percent) and minor patchy Ca pyroxene. Bulk chemical analysis yielded Fe_total 21.60 wt. percent, Fe/SiO₂0.55, SiO₂/MgO 1.53 and Fe^O/Fe_total 0.29. Barred olivine, radiating pyroxene and porphyritic chondrules, all with ill-defined outlines, occur in the meteorite. Most chemical and mineralogical features characterize the Homewood meteorite as an L6 (hypersthene) chondrite. The presence of maskelynite, the undulatory extinction, extensive fracturing and pervasive mosaicism of olivine, and the poor definition of chondrule outlines suggest that the Homewood meteorite has been shocked in the range of 300–350 kbar.     

THE ORO GRANDE,NEW MEXICO,CHONDRITE AND ITS LITHIC INCLUSION

The Oro Grande, New Mexico, U.S.A., chondrite was found in 1971. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 19.3 mole percent), orthopyroxene (Fs 16.2 mole percent), diopside, feldspar (An 13.6 mole percent), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. A bulk chemical analysis of the meteorite shows the following results (weight percent): Fe 0.84, Ni 1.46, Co 0.07, FeS 3.62, SiO₂ 34.18, TiO₂ 0.14, Al₂O₃ 1.83, Cr₂O₃ 0.55, Fe₂O₃ 21.25, FeO 9.13, MnO 0.31, MgO 21.52, CaO 1.72, Na₂O 0.70, K₂O 0.08, P₂O₅ 0.25, H₂O+ 2.14, H₂O^- 0.40, C 0.22, Sum 100.41. On the basis of composition and texture, the Oro Grande meteorite is classified as an H5 chondrite. A large lithic fragment (～5 mm long) with a very fine-grained texture different from that of the host meteorite was analyzed for bulk composition using the broad beam of an electron microprobe, and was found to be enriched in Ca, Al, Na, and K, and depleted in Mg and Fe relative to the bulk composition of the host meteorite. Its mineral compositions, however, are very similar to those of the host. It is suggested that the fragment is not a xenolith of a previously undescribed type of achondrite, but is probably an impact-produced partial melt of the host chondrite or a fragment of an unusually large chondrule.     

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.     

K2O‐rich trapped melt in olivine in the Nakhla meteorite: Implications for petrogenesis of nakhlites and evolution of the Martian mantle

We used new analytical and theoretical methods to determine the major and minor element compositions of the primary trapped liquid (PTLs) represented by melt inclusions in olivine and augite in the Martian clinopyroxenite, Nakhla, for comparison with previously proposed compositions for the Nakhla (or nakhlite) parent magma. We particularly focused on obtaining accurate K₂O contents, and on testing whether high K₂O contents and K₂O/Na₂O ratios obtained in previous studies of melt inclusions in olivine in Nakhla could have been due to unrepresentative sampling, systematic errors arising from electron microprobe techniques, late alteration of the inclusions, and/or boundary layer effects. Based on analyses of 35 melt inclusions in olivine cores, the PTL in olivine, PTL_oliv, contained (by wt) approximately 47% SiO₂, 6.3% Al₂O₃, 9.6% CaO, 1.8% K₂O, and 0.9% Na₂O, with K₂O/Na₂O = 2.0. We infer that the high K₂O content of PTL_oliv is not due to boundary layer effects and represents a real property of the melt from which the host olivine crystallized. This melt was cosaturated with olivine and augite. Its mg# is model‐dependent and is constrained only to be ≥19 (equilibrium Fo = 40). Based on analyses of 91 melt inclusions in augite cores, the PTL in augite, PTL_aug, contained (by wt) 53–54% SiO₂, 7–8% Al₂O₃, 0.8–1.1% K₂O, and 1.1–1.4% Na₂O, with K₂O/Na₂O = 0.7–0.8. This K₂O content and K₂O/Na₂O ratio are significantly higher than inferred in studies of melt inclusions in augite in Nakhla by experimental rehomogenization. PTL_aug was saturated only with augite, and in equilibrium with augite cores of mg# 62. PTL_aug represents the Nakhla parent magma, and does not evolve to PTL_oliv by fractional crystallization. We therefore conclude that olivine cores in Nakhla (and, by extension, other nakhlites) are xenocrystic. We propose that PTL_oliv and PTL_aug were generated from the same source region. PTL_oliv was generated first and emplaced to form olivine‐rich cumulate rocks. Shortly thereafter, PTL_aug was generated and ascended through these olivine‐rich cumulates, incorporating fragments of wallrock that became the xenocrystic olivine cores in Nakhla. The Nakhla (nakhlite) mantle source region was pyroxenitic with some olivine, and could have become enriched in K relative to Na via metasomatism. A high degree of melting of this source produced the silica‐poor, alkali‐rich magma PTL_oliv. Further ascension and decompression of the source led to generation of the silica‐rich, relatively alkali‐poor magma PTL_aug. Potassium‐rich magmas like those involved in the formation of the nakhlites represent an important part of the diversity of Martian igneous rocks.     

CLAST-LADEN MELT-ROCK FRAGMENT IN THE ADAMS COUNTY,COLORADO, H5 CHONDRITE

The Adams County, Colorado, H5 chondrite contains a lithic fragment, 1 cm in size, that is texturally and mineralogically quite different from the chondritic host. It is composed of: a groundmass of fine-grained euhedral to subhedral olivine (3–15 μm) and interstitial glass enclosing larger olivine and pyroxene grains (0.15-0.5 mm; about 15 vol %); an assemblage of enstatite grains (subfragment within) and an assemblage of olivine plus orthopyroxene (a second subfragment); and about 11 vol % grains of mixed troilite and nickel-iron metal. Analyses yielded these results: (i) olivine grains of the fragment groundmass have a compositional range (Fa_12–45) and most grains contain substantial CaO and Cr₂O₃ (～ 0.20 and 0.30 avg. wt%, respectively); interstitial glass has ～ 55 wt% SiO₂; (ii) larger olivine grains of the fragment are similarly high in CaO and Cr₂O₃ and also have a wide FeO/MgO range; one unusual pyroxene is an Mg-rich pigeonite; (iii) the metal is martensite in composition (11–14 wt% Ni); and (iv) major and trace element analyses by INAA indicate an H-group bulk composition for the entire 1 cm lithic fragment. On the basis of its texture and bulk and mineral compositions, the fragment is interpreted to represent unequilibrated H-group material that was partly melted by impact. The Ca- and Cr-enriched groundmass olivine and interstitial glass resulted from rapid crystallization of the chondritic melt. The Ca- and Cr-enriched larger silicate grains, including the enstatite sub-fragment and the pigeonite grain, are residual, unmelted clasts from the target material (this is supported by the presence of similar material in actual H3 chondrites). Further impact brecciation of the clast-laden melt material, and resultant impact-splashing accounts for the presence of the fragment in the H-group Adams County host and documents the coexistence of unequilibrated and equilibrated H-group material as surface regolith on one parent body.     

PIANCALDOLI METEORITE: CHEMISTRY,MINERALOGY AND PETROLOGY

The fall occurred near Piancaldoli, Florence, Italy, at 19.14 U.T. on the 10th August 1968. The fireball broke up in the atmosphere producing a cloud like a balloon. The trajectory and the terminal point were calculated, leading to the recovery of three small meteoritic fragments, found on the roof of a house. Chemical analysis gave the following results: SiO₂ 40.80; TiO₂ 0.15; Al₂O₃ 2. 70; Cr₂O₃ 0.47; FeO 17.20; MnO 0.07; MgO 25.18; CaO 1.95; Na₂O 0.64; K₂O 0.07; P₂O₅ 0.20; NiS 0.93; FeS 6.24; Fe° 2.40; Ni° 0.40; Co 0.05; sum 99.45. In the lithic portion of the meteorite the following minerals were found: both clino and orthopyroxenes (En = 76 to 98%), olivines (Fo = 66 to 98%), troilite, pyrrhotite, pentlandite, kamacite, ilmenite, apatite, merillite, schreibersite, chromite and Henderson phase. From all the mineralogical and petrological data, we conclude that the Piancaldoli meteorite is an “unequilibrated ordinary chondrite,” LL3. The microbrecciated structure of the rock and some shock features were observed, while the rock as a whole is unshocked, suggesting that these features were caused by impact events which took place during the accretion of the parent body.     

Characterization of weathering and heterogeneous mineral phase distribution in brachinite Northwest Africa 4872

Terrestrial weathering of hot desert achondrite meteorite finds and heterogeneous phase distributions in meteorites can complicate interpretation of petrological and geochemical information regarding parent‐body processes. For example, understanding the effects of weathering is important for establishing chalcophile and siderophile element distributions within sulfide and metal phases in meteorites. Heterogeneous mineral phase distribution in relatively coarsely grained meteorites can also lead to uncertainties relating to compositional representativeness. Here, we investigate the weathering and high‐density (e.g., sulfide, spinel, Fe‐oxide) phase distribution in sections of ultramafic achondrite meteorite Northwest Africa (NWA) 4872. NWA 4872 is an olivine‐rich brachinite (Fo_{63.6 ± 0.5}) with subsidiary pyroxene (Fs_9.7 ± 0.1Wo_{46.3 ± 0.2}), Cr‐spinel (Cr# = 70.3 ± 1.1), and weathered sulfide and metal. Raman mapping confirms that weathering has redistributed sulfur from primary troilite, resulting in the formation of Fe‐oxide (‐hydroxide) and marcasite (FeS₂). From Raman mapping, NWA 4872 is composed of olivine (89%), Ca‐rich pyroxene (0.4%), and Cr‐spinel (1.1%), with approximately 7% oxidized metal and sulfide and 2.3% marcasite‐dominated sulfide. Microcomputed tomography (micro‐CT) observations reveal high‐density regions, demonstrating heterogeneities in mineral distribution. Precision cutting of the largest high‐density region revealed a single 2 mm Cr‐spinel grain. Despite the weathering in NWA 4872, rare earth element (REE) abundances of pyroxene determined by laser‐ablation inductively coupled plasma mass spectrometry (LA‐ICP‐MS) indicate negligible modification of these elements in this mineral phase. The REE abundances of mineral grains in NWA 4872 are consistent with formation of the meteorite as the residuum of the partial melting process that occurred on its parent body. LA‐ICP‐MS analyses of sulfide and alteration products demonstrate the mobility of Re and/or Os; however, highly siderophile element (HSE) abundance patterns remain faithful recorders of processes acting on the brachinite parent body(ies). Detailed study of weathering and phase distribution offers a powerful tool for assessing the effects of low‐temperature alteration and for identifying robust evidence for parent‐body processes.     

Mineralogy of a refractory inclusion in the Allende (C3V) meteorite

Abstract— A spherical, 220-μm diameter, spinel-hibonite-perovskite inclusion from the Allende C3V meteorite contains a central hibonite cluster with an angular boundary. This central hibonite is enclosed within spinel that is zoned from Mg-rich at the hibonite boundary to more Fe-rich at the inclusion boundary. This spinel zone includes lath-shaped hibonites usually oriented subradial to the central hibonites. Two textural types of perovskites are present as exsolution from the central hibonite and as equidimensional grains within both the central hibonite and spinel. These second perovskites have exsolution lamellae of Al₂O₃. Within the central hibonite and adjacent to some equidimensional perovskites, a fine porous phase interpreted as alteration has a composition of nearly pure Al₂O₃ with minor amounts of Na and Si. This is possibly either an intergrowth of corundum and nepheline or a modified Al₂O₃, β-alumina. The central hibonites and equidimensional perovskites are considered relict grains on which the spinel-hibonite layer crystallized. The relict material had undergone slow cooling in a previous event to produce exsolution of original high-temperature compositions. Later alteration caused breakdown of hibonite to give an Al₂O₃-rich phase. This inclusion represents a composite body which formed in a Ca-Al-rich environment.     

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.     

SHERGOTTY METEORITE: MINERALOGY,PETROGRAPHY AND MINOR ELEMENTS

The unusual achondrite Shergotty resembles terrestrial diabases, and textural and chemical evidence indicates pre-settling and post-settling crystallization of zoned augite (En₄₈Fs₁₉Wo₃₃-En₂₅Fs₄₇Wo₂₈) and pigeonite (En₆₁Fs₂₆Wo₁₃-En₂₁Fs₆₁Wo₁₈) coupled with late crystallization of plagioclase (Ab₄₃An₅₆/Or₁-Ab₅₆An₄₁Or₃: now shocked to maskelynite), titanomagnetite-ilmenite composite grains, mesostasis (normative Qz₃₄Ab₂₁An₅Or₃₈Fs₂, assuming Fe as ferrous), whitlockite, pyrrhotite (Fe_0.94S), fayalite (Fo₁₀), baddeleyite and chlorapatite. The oxide compositions (Usp₆₂Mt₃₈, Al₂O₃ 2.4, Cr₂O₃ 0.8 wt %; Ilm₉₅Hm₅) indicate ～ 850 °C and log oxygen fugacity ? 14, while the occurrence of fayalite rims on mesostasis next to ilmenite indicates 890 °C. Bearing in mind experimental uncertainties, these data are consistent with late-stage crystallization under relatively high oxygen fugacity, as indicated by coexistence of fayalite, Ti-magnetite and a silica glass. The high alkali content of the maskelynite and mesostasis, coupled with the redox state, indicates that the Shergotty meteorite resembles terrestrial basalts more than any other meteorites. Nevertheless the absence of H₂O, as shown by the occurrence of phosphorus in whitlockite rather than in hydroxylapatite, distinguish the Shergotty achondrite from typical terrestrial diabases. Whereas the FeO/MnO ratios of pyroxenes from the Moon, Earth and several differentiated meteorites are independent of FeO, the ratio for Shergotty pyroxenes changes from 30 to 40 with increasing FeO, and the linear trend extrapolates to 0.2 MnO for zero iron. Hence caution is needed in using FeO/MnO as a planetary indicator. For pyroxenes, Na is almost independent of Fe/Mg while Ti increases and Cr decreases with increasing Fe/Mg. Maskelynite contains 0.5–0.25 wt % K₂O, 0.6 wt % FeO, 0.04 TiO₂, 0.04–0.07 MgO, ～ 0.01 BaO and 0.02–0.03 P₂O₅. A bulk analysis calculated from the mode and compositions of the minerals matches quite well with two bulk chemical analyses but not with a third.     

THE NARAGH METEORITE: A NEW OLIVINE-BRONZITE CHONDRITE FALL

At 9:20 A.M. on August 18, 1974, a stony meteorite of approximately 3200 grams struck the roof of a secondary school at Naragh, Central Iran, (51°30′E, 33°45′N). The ellipsoidal dark-gray meteorite was 17 × 15 × 13 cm (density 3.62 gr/cm³). XRF and wet chemical analysis yields the bulk composition of the meteorite as follows in weight percent: Fe 11.95, Ni 1.05, Co 0.07, FeS 5.49, SiO₂ 37.15, TiO₂ 0.15, Al₂O₃ 2.43, Cr₂O₃0.62, FeO 14.25, MnO 0.23, MgO 23.79, CaO 1.61, Na₂O 0.92, K₂O 0.08, P₂O₅ 0.26. Modal mineral contents (in volume percent) are olivine 40, orthopyroxene 25, clinopyroxene 3, plagioclase 10.5, chromite 0.80, phosphate 0.70, troilite 6, metal phases 14. The meteorite is fine-grained, with average grain size about 0.4–0.6 mm and contains numerous recrystallized glassy chondrules. Olivine occurs as laths and radiating crystals in chondrules and as coarse-grained phenocrysts and interstitial microcrystalline grains in the matrix. These olivines have relatively uniform composition (Fo_80–82Fa_20–18). Fine-grained skeletal orthopyroxenes of average composition (En₁₆Fs₈₂Wo₀₁) are inter-grown with olivine in both chondrules and matrix. Clinopyroxene and plagioclase of average composition (En_6.5Fs₄₈Wo_45.5) and (Ab₈₂An₁₂Or₀₆) respectively, are evenly distributed in the matrix, together with kamacite (Fe_92–95), plessite (Fe_69.6–82.2) and taenite (Fe_46.7–66.1), troilite (Ni-free) and chromite grains. The high ratios of total Fe to SiO₂ of 0.71, metallic Fe to total Fe of 0.54, and SiO₂ to MgO of 1.56 in the bulk composition, the Fa component of olivine grains of 17.5–19.6, and the high Ca content of orthopyroxenes between 0.53 and 0.87 wt % suggest that the Naragh meteorite belongs to the H-group and petrologic type 6 of Van Schmus and Wood (1967) classification. In addition, the occurrence of fine-grained clear sodic plagioclase, the presence of numerous recrystallized chondrules with homogeneous silicate minerals, and the absence of Ni in the sulfide phase indicate that the Naragh meteorite has been metamorphosed after the initial crystallization in the parental body.     

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.