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 Published and unpublished data on minor and trace elements in the bulk meteorite and in the pyroxene are presented in tabular form.     

Geochemistry and Sm‐Nd chronology of a Stannern‐group eucrite,Northwest Africa 7188

We report the results of a detailed study of the basaltic eucrite Northwest Africa (NWA) 7188, including its mineralogical and bulk geochemical characteristics, oxygen isotopic composition, and ^147,146Sm‐^143,142Nd mineral isochron ages. The texture and chemical composition of pyroxene and plagioclase demonstrate that NWA 7188 is a monomict eucrite with a metamorphic grade of type 4. The oxygen isotopic composition and the Fe/Mn ratios of pyroxene confirmed that NWA 7188 belongs to the howardite–eucrite–diogenite meteorite suite, generally considered to originate from asteroid 4 Vesta. Whole‐rock TiO₂, La, and Hf concentrations and a CI chondrite‐normalized rare earth element pattern are in good agreement with those of representative Stannern‐group eucrites. The ^147,146Sm‐^143,142Nd isochrons for NWA 7188 yielded ages of 4582 ± 190 and 4554 +17/?19 Ma, respectively. The closure temperature of the Sm‐Nd system for different fractions of NWA 7188 was estimated to be >865 °C, suggesting that the Sm‐Nd decay system has either been resistant to reheating at ~800 °C during the global metamorphism or only partially reset. Therefore, the ¹⁴⁶Sm‐¹⁴²Nd age of NWA 7188 corresponds to the period of initial crystallization of basaltic magmas and/or global metamorphism on the parent body, and is unlikely to reflect Sm‐Nd disturbance by late reheating and impact events. In either case, NWA 7188 is a rare Stannern‐group eucrite that preserves the chronological information regarding the initial crustal evolution of Vesta.     

Phase equilibria of the Shergotty meteorite: Constraints on pre‐eruptive water contents of martian magmas and fractional crystallization under hydrous conditions

Abstract— An experimental investigation of the Shergotty meteorite was performed at 0.1 MPa under anhydrous conditions at the quartz‐fayalite‐magnetite buffer and at 100 and 200 MPa under H₂O‐saturated conditions at the nickel‐nickel oxide buffer. The results of these experiments are used to infer magmatic conditions recorded by co‐crystallization of augite and pigeonite phenocrysts found in Shergotty and to investigate the effect of H₂O on fractional crystallization paths followed by shergottite magmas. The phase relations and compositions of the homogeneous magnesian pyroxene cores in Shergotty are most closely approximated by crystallization under H₂O‐saturated conditions at 1120 °C (± 10 °C) and 56 MPa (± 18 MPa), corresponding to dissolved H₂O contents of 1.8 wt% (± 0.6 wt%) and a depth of 5 km (± 1.5 km) in the martian crust (uncertainties are 2s? values). The Shergotty magma then lost this water during ascent and eruption. Fractional crystallization of the Shergotty magma under anhydrous conditions produces liquids that follow a strong Fe‐enrichment trend at nearly constant SiO₂. Crystallization under H₂O‐saturated conditions generates derivative liquids, depleted in FeO and Al₂O₃ and enriched in SiO₂, that are compositionally similar to the Mars Pathfinder andesite rock composition. The presence of ～1.8 wt% water in Shergotty parental magmas could result from assimilation of hydrated crustal materials or from dehydration of hydrous phases in the mantle source region.     

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.     

QUE 94204: A primitive enstatite achondrite produced by the partial melting of an E chondrite‐like protolith

Abstract– Queen Alexandra Range (QUE) 94204, an enstatite achondrite, is a coarse‐grained, highly recrystallized, chondrule‐free and unbrecciated rock dominated (about 70 vol%) by anhedral, equigranular crystals of orthoenstatite of nearly endmember composition (Fs_0.1–0.4, Wo_0.3–0.4) with interstitial plagioclase, kamacite, and troilite. Abundance of approximately 120° triple junctions and the close association of metal–sulfide and plagioclase‐rich melts indicate that QUE 94204 has undergone limited partial melting with inefficient melt extraction. Mineral chemistry indicates a high degree of thermal metamorphism. Kamacite in QUE 94204 contains between 2.09 and 2.55 wt% Si, similar to highly metamorphosed EL chondrites. Plagioclase has between 4.31 and 6.66 wt% CaO, higher than other E chondrites but closer in composition to plagioclase from metamorphosed EL chondrites. QUE 94204 troilite contains up to 2.55 wt% Ti, consistent with extensive thermal metamorphism of an E chondrite‐like precursor. Results presented in this study indicate that QUE 94204 is the result of low degree, (about 5–20 vol%, probably toward the lower end of this range) partial melting of an E chondrite protolith. Textural and chemical evidence suggests that during the metamorphism of QUE 94204, melts formed first at the Fe,Ni‐FeS cotectic near approximately 900 °C, followed by plagioclase‐pyroxene silicate partial melts near approximately 1100 °C. Neither the Fe,Ni‐FeS nor the plagioclase‐pyroxene melts were efficiently segregated or extracted. QUE 94204 belongs to a grouplet of similar “primitive enstatite achondrites” that are analogous to the acapulcoites‐lodranites, but that have resulted from the partial melting of an E chondrite‐like protolith.     

CHEMICAL COMPOSITION,PETROGRAPHY AND MINERALOGY OF THE SHIBAYAMA CHONDRITE FOUND IN SHIBAYAMA-MACHI,SANBU-GUN,CHIBA-KEN,JAPAN

In April 1969, the chondrite was accidentally found in the side wall of the vegetable storage excavated at Shibayama-machi, Sanbu-gun, Chiba-ken, Japan, by Mr. A. Ishii and his grandson, Mr. S. Ito. The chondrite named Shibayama has been weathered thoroughly for a long period of burial underground. The bulk chemical composition, especially total Fe (21.41%) and ratios of Fe_total/SiO₂(0.557), SiO₂/MgO (1.59) and molar composition of olivine (Fa₂₃) and pyroxene (Fs₂₂) as well as mineral composition, indicate that Shibayama is a typical olivine-hypersthene chondrite. If the oxidized Fe is assumed only from metallic Fe, the original metallic Fe (7.75%) and Fe_metal/Fe_total(0.361) also support the above conclusion. From the well-recrystallized texture, indistinct and obliterated chondrule-matrix boundary, homogeneous composition of olivine and pyroxene, absence of igneous glass, and interstitial and well-developed plagioclase, this chondrite could be classified in petrologic type 6. Mosaic texture, kink bands, undulatory extinction of silicate grains and maskelynitization of plagioclase indicate that Shibayama suffered from a heavy shock effect, as is seen in other L-6 group chondrites.     

Eutectic metal + troilite + Fe‐Mn‐Na phosphate + Al‐free chromite assemblage in shock‐produced chondritic melt of the Yanzhuang chondrite

An assemblage with FeNi metal, troilite, Fe‐Mn‐Na phosphate, and Al‐free chromite was identified in the metal‐troilite eutectic nodules in the shock‐produced chondritic melt of the Yanzhuang H6 meteorite. Electron microprobe and Raman spectroscopic analyses show that a few phosphate globules have the composition of Na‐bearing graftonite (Fe_,Mn,Na)₃(PO₄)₂, whereas most others correspond to Mn‐bearing galileiite Na(Fe,Mn)₄(PO₄)₃ and a possible new phosphate phase of Na₂(Fe,Mn)₁₇(PO₄)₁₂ composition. The Yanzhuang meteorite was shocked to a peak pressure of 50 GPa and a peak temperature of approximately 2000 °C. All minerals were melted after pressure release to form a chondritic melt due to very high postshock heat that brought the chondrite material above its liquidus. The volatile elements P and Na released from whitlockite and plagioclase along with elements Cr and Mn released from chromite are concentrated into the shock‐produced Fe‐Ni‐S‐O melt at high temperatures. During cooling, microcrystalline olivine and pyroxene first crystallized from the chondritic melt, metal‐troilite eutectic intergrowths, and silicate melt glass finally solidified at about 950–1000 °C. On the other hand, P, Mn, and Na in the Fe‐Ni‐S‐O melt combined with Fe and crystallized as Fe‐Mn‐Na phosphates within troilite, while Cr combined with Fe and crystallized as Al‐free chromite also within troilite.     

Secondary‐volatiles linked metallic iron in eucrites: The dual‐origin metals of Camel Donga

The unique occurrence of abundant (~1 vol%) near‐pure‐Fe metal in the Camel Donga eucrite is more complicated than previously believed. In addition to that component of groundmass metal, scattered within the meteorite are discrete nodules of much higher kamacite abundance. We have studied the petrology and composition of two of these nodules in the form of samples we call CD2 and CD3. The nodules are ovoids 11 (CD2) to 15 (CD3) mm across, with metal, or inferred preweathering metal, abundances of 12–17 vol% (CD2 is unfortunately quite weathered). The CD3 nodule also includes at its center a 5 mm ovoid clumping (6 vol%) of F‐apatite. Both nodules are fine‐grained, so the high Fe metal and apatite contents are clearly not flukes of inadequate sampling. The metals within the nodules are distinctly Ni‐rich (0.3–0.6 wt%) compared to the pure‐Fe (Ni generally 0.01 wt%) groundmass metals. Bulk analyses of three pieces of the CD2 nodule show that trace siderophile elements Ir, Os, and Co are commensurately enriched; Au is enriched to a lesser degree. The siderophile evidence shows the nodules did not form by in situ reduction of pyroxene FeO. Moreover, the nodules do not show features such as silica‐phase enrichment or pyroxene with reduced FeO (as constrained by FeO/MgO and especially FeO/MnO) predicted by the in situ reduction model. The oxide minerals, even in groundmass samples well away from the nodules, also show little evidence of reduction. Although the nodule boundaries are generally sharp, groundmass‐metal Ni content is anti‐correlated with distance from the CD3 nodule. We infer that the nodules represent materials that originated within impactors into the Camel Donga portion of the eucrite crust, but probably were profoundly altered during later metamorphism/metasomatism. Origin of the pure‐Fe groundmass metal remains enigmatic. In situ reduction probably played an important role, and association in the same meteorite of the Fe‐nodules is probably significant. But the fluid during alteration was probably not (as previously modeled) purely S and O, of simple heat‐driven internal derivation. We conjecture a two‐stage metasomatism, as fluids passed through Camel Donga after impact heating of volatile‐rich chondritic masses (survivors of gentle accretionary impacts) within the nearby crust. First, reduction to form troilite may have been triggered by fluids rich in S₂ and CO (derived from the protonodules?), and then in a distinct later stage, fluids were (comparatively) H₂O‐rich, and thus reacted with troilite to form pure‐Fe metal along with H₂S and SO₂. The early eucrite crust was in places a dynamic fluid‐bearing environment that hosted complex chemical processes, including some that engendered significant diversity among metal+sulfide alterations.     

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.     

Experimental studies of magnetite formation in the solar nebula

Abstract— Oxidation of Fe metal and Gibeon meteorite metal to magnetite via the net reaction 3 Fe (metal) + 4 H₂O (gas) = Fe₃O₄ (magnetite) + 4 H₂ (gas) was experimentally studied at ambient atmospheric pressure at 91–442 °C in H₂ and H₂-He gas mixtures with H₂/H₂O molar ratios of ～4–41. The magnetite produced was identified by x-ray diffraction. Electron microprobe analyses showed 3.3 wt% NiO and 0.24 wt% CoO (presumably as NiFe₂O₄ and CoFe₂O₄) in magnetite formed from Gibeon metal. The NiO and CoO concentrations are higher than expected from equilibrium between metal and oxide under the experimental conditions. Elevated NiO contents in magnetite were also observed by metallurgists during initial stages of oxidation of Fe-Ni alloys. The rate constants for magnetite formation were calculated from the weight gain data using a constant surface area model and the Jander, Ginstling-Brounshtein, and Valensi-Carter models for powder reactions. Magnetite formation followed parabolic (i.e., diffusion-controlled) kinetics. The rate constants and apparent activation energies for Fe metal and Gibeon metal are: These rate constants are significantly smaller than the parabolic rate constants for FeS growth on Fe metal in H₂S-H₂ gas mixtures containing 1000 or 10 000 ppmv H₂S (Lauretta et al., 1996a). The experimental data for Fe and Gibeon metal are used to model the reaction time of Fe alloy grains in the solar nebula as a function of grain size and temperature. The reaction times for 0.1–1 μm radius metal grains are generally within estimated lifetimes of the solar nebula (0.1–10 Ma). However, the calculated reaction times are probably lower limits, and further study of magnetite formation at larger H₂/H₂O ratios, at lower temperatures and pressures, and as a function of metal alloy composition is needed for further modeling of nebular magnetite formation.     

Identification of magnetite in lunar regolith breccia 60016: Evidence for oxidized conditions at the lunar surface

Lunar regolith breccias are temporal archives of magmatic and impact bombardment processes on the Moon. Apollo 16 sample 60016 is an “ancient” feldspathic regolith breccia that was converted from a soil to a rock at ~3.8 Ga. The breccia contains a small (70 × 50 μm) rock fragment composed dominantly of an Fe‐oxide phase with disseminated domains of troilite. Fragments of plagioclase (An_95‐97), pyroxene (En_74‐75, Fs_21‐22,Wo_3‐4), and olivine (Fo_66‐67) are distributed in and adjacent to the Fe‐oxide. The silicate minerals have lunar compositions that are similar to anorthosites. Mineral chemistry, synchrotron X‐ray absorption near edge spectroscopy (XANES) and X‐ray diffraction (XRD) studies demonstrate that the oxide phase is magnetite with an estimated Fe³⁺/ΣFe ratio of ~0.45. The presence of magnetite in 60016 indicates that oxygen fugacity during formation was equilibrated at, or above, the Fe‐magnetite or wüstite–magnetite oxygen buffer. This discovery provides direct evidence for oxidized conditions on the Moon. Thermodynamic modeling shows that magnetite could have been formed from oxidization‐driven mineral replacement of Fe‐metal or desulphurisation from Fe‐sulfides (troilite) at low temperatures (<570 °C) in equilibrium with H₂O steam/liquid or CO₂ gas. Oxidizing conditions may have arisen from vapor transport during degassing of a magmatic source region, or from a hybrid endogenic–exogenic process when gases were released during an impacting asteroid or comet impact.     

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.     

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.     

Thermodynamic constraints on fayalite formation on parent bodies of chondrites

Abstract— Thermochemical equilibria are calculated in the multicomponent gas‐solution‐rock system in order to evaluate the formation conditions of fayalite, (Fe_0.88–1.0Mg_0.12–0)₂SiO₄, Fa_88–100, in unequilibrated chondrites. Effects of temperature, pressure, water/rock ratio, rock composition, and progress of alteration are evaluated. The modeling shows that fayalite can form as a minor secondary and transient phase with and without aqueous solution. Fayalite can form at temperatures below ?350 °C, but only in a narrow range of water/rock ratios that designates a transition between aqueous and metamorphic conditions. Pure fayalite forms at lower temperatures, higher water/rock ratios, and elevated pressures that correspond to higher H₂/H₂O ratios. Lower pressure and water/rock ratios and higher temperatures favor higher Mg content in olivine. In equilibrium assemblages, fayalite usually coexists with troilite, kamacite, magnetite, chromite, Ca‐Fe pyroxene, and phyllosilicates. Formation of fayalite can be driven by changes in temperature, pressure, H₂/H₂O, and water/rock ratios. However, in fayalite‐bearing ordinary and CV3 carbonaceous chondrites, the mineral could have formed during the aqueous‐to‐metamorphic transition. Dissolution of amorphous silicates in matrices and/or silica grains, as well as low activities of Mg solutes, favored aqueous precipitation of fayalite. During subsequent metamorphism, fayalite could have formed through the reduction of magnetite and/or dehydration of ferrous serpentine. Further metamorphism should have caused reductive transformation of fayalite to Ca‐Fe pyroxene and secondary metal, which is consistent with observations in metamorphosed chondrites. Although bulk compositions of matrices/chondrites have only a minor effect on fayalite stability, specific alteration paths led to different occurrences, quantities, and compositions of fayalite in chondrites.     

Incremental melting in the ureilite parent body: Initial composition,melting temperatures,and melt compositions

Ureilites are carbon‐rich ultramafic achondrites that have been heated above the silicate solidus, do not contain plagioclase, and represent the melting residues of an unknown planetesimal (i.e., the ureilite parent body, UPB). Melting residues identical to pigeonite‐olivine ureilites (representing 80% of ureilites) have been produced in batch melting experiments of chondritic materials not depleted in alkali elements relative to the Sun’s photosphere (e.g., CI, H, LL chondrites), but only in a relatively narrow range of temperature (1120 ºC–1180 ºC). However, many ureilites are thought to have formed at higher temperature (1200 ºC–1280 ºC). New experiments, described in this study, show that pigeonite can persist at higher temperature (up to 1280 ºC) when CI and LL chondrites are melted incrementally and while partial melts are progressively extracted. The melt productivity decreases dramatically after the exhaustion of plagioclase with only 5–9 wt% melt being generated between 1120 ºC and 1280 ºC. The relative proportion of pyroxene and olivine in experiments is compared to 12 ureilites, analyzed for this study, together with ureilites described in the literature to constrain the initial Mg/Si ratio of the UPB (0.98–1.05). Experiments are also used to develop a new thermometer based on the partitioning of Cr between olivine and low‐Ca pyroxene that is applicable to all ureilites. The equilibration temperature of ureilites increases with decreasing Al₂O₃ and Wo contents of pyroxene and decreasing bulk REE concentrations. The UPB melted incrementally, at different fO₂, and did not cool significantly (0 ºC–30 ºC) prior to its disruption. It remained isotopically heterogenous, but the initial concentration of major elements (SiO₂, MgO, CaO, Al₂O₃, alkali elements) was similar in the different mantle reservoirs.     

Petrology and Pairing of Mesosiderites from Victoria Land,Antarctica

Abstract— The Allan Hills mesosiderites A77219, A81059 and A81098 are classified as subgroup 1B (Hewins, 1984), on the basis of very fine-grained silicate matrix, low plagioclase content and absence of highly ferroan pyroxenes. Since they are so similar petrologically, it is reasonable to pair them. ALHA 81208, a highly weathered orthopyroxenite, is probably a clast from one of the Allan Hills mesosiderites. Reckling Peak A80258, is a Floran 2B or Hewins 4B mesosiderite. It contains reversely zoned orthopyroxene clasts in a sparse matrix with interstitial/poikilitic plagioclase and highly magnesian (chadacryst) orthopyroxene (close to En₈₀). All pyroxene is much lower in FeO/MnO than Allan Hills mesosiderite pyroxene of similar FeO content. The other Reckling Peak mesosiderites A79015, A80229, A80246 and A80263 contain orthopyroxene and recrystallized orthopyroxenite clasts in a metal-troilite matrix. Orthopyroxenite clasts in ALH A81059 are very similar texturally and modally to RKPA 79015 orthopyroxenite, but differ in pyroxene composition. Orthopyroxene in RKPA 79015 (Prinz et al., 1982) is very similar in Fe/Mg and Fe/Mn to the cores of (reversely zoned) pyroxene clasts in RKPA 80258. On this basis, RKPA 80258 is related to the other Reckling Peak mesosiderites and they could all be paired, assuming that three components (metal, pyroxenite and silicate matrix) were very irregularly mixed in these breccias. Pairing is problematical, in that specimens of a polymict breccia can be so different that they would not be paired if they were not known to have fallen together. The silicate fraction of mesosiderites ranges from diogenitic (RKPA 79015) to analogous to polymict eucrite (Dyarrl Island) although the silicate fractions are not equivalent in detail. The mesosiderite subdivision scheme is amended recognizing this, permitting the classification of the formerly “anomalous” RKPA 79015.     

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.     

Origin of the metamorphosed clasts in the CV3 carbonaceous chondrite breccias of Graves Nunataks 06101, Vigarano,Roberts Massif 04143, and Yamato‐86009

We observed metamorphosed clasts in the CV3 chondrite breccias Graves Nunataks 06101, Vigarano, Roberts Massif 04143, and Yamato‐86009. These clasts are coarse‐grained polymineralic rocks composed of Ca‐bearing ferroan olivine (Fa_24–40, up to 0.6 wt% CaO), diopside (Fs_7–12Wo_44–50), plagioclase (An_52–75), Cr‐spinel (Cr/[Cr + Al] = 0.4, Fe/[Fe + Mg] = 0.7), sulfide and rare grains of Fe‐Ni metal, phosphate, and Ca‐poor pyroxene (Fs₂₄Wo₄). Most clasts have triple junctions between silicate grains. The rare earth element (REE) abundances are high in diopside (REE ~3.80–13.83 × CI) and plagioclase (Eu ~12.31–14.67 × CI) but are low in olivine (REE ~0.01–1.44 × CI) and spinel (REE ~0.25–0.49 × CI). These REE abundances are different from those of metamorphosed chondrites, primitive achondrites, and achondrites, suggesting that the clasts are not fragments of these meteorites. Similar mineralogical characteristics of the clasts with those in the Mokoia and Yamato‐86009 breccias (Jogo et al. 2012 ) suggest that the clasts observed in this study would also form inside the CV3 chondrite parent body. Thermal modeling suggests that in order to reach the metamorphosed temperatures of the clasts of >800 °C, the clast parent body should have accreted by ~2.5–2.6 Ma after CAIs formation. The consistency of the accretion age of the clast parent body and the CV3 chondrule formation age suggests that the clasts and CV3 chondrites could be originated from the same parent body with a peak temperature of 800–1100 °C. If the body has a peak temperature of >1100 °C, the accretion age of the body becomes older than the CV3 chondrule formation age and multiple CV3 parent bodies are likely.     

The condensation and fractionation of refractory lithophile elements

It has long been recognized that Cr, Mg, and Si are fractionated in chondritic material along with, but to a much lesser extent than, a large group of more refractory elements. Reasoning that this might imply some unique distribution at the time of fractionation, the patterns have been reexamined. It now appears as if two distinct fractionation patterns can be resolved: one involving ordinary and enstatite chondrites and the other involving carbonaceous chondrites, the Earth, the Moon, and the eucrite parent body. Significantly, the two trends inevitably intersect at C1 composition. Ordinary and enstatite chondrites appear to have evolved from C1 composition via the removal of about 40 and 56% of a high-temperature condensate. Another high-temperature condensate, with a distinctly different composition, appears to be enriched in the carbonaceous chondrites, the Moon, and possibly the Earth, but depleted in the eucrite parent body. The compositions of these two components are constrained to fall on the appropriate mixing lines. These lines intersect the condensation path at two points, one where Mg₂SiO₄ has just begun to condense (～20%) and a second where Mg₂SiO₄ was almost completely condensed (～90%). This represents about an 80° temperature difference. But it is within this range that the largest fraction of planetary matter (Mg, Si, and Fe) condenses. Conceivably the relatively sudden appearance of large amounts of condensed material is in some way related to the fractionation process, although the exact relationship cannot be specified.     

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.