Frontier Mountain meteorite specimens of the acapulcoite‐lodranite clan: Petrography,pairing, and parent‐rock lithology of an unusual intrusive rock

Abstract— In this paper we reconstruct the heterogeneous lithology of an unusual intrusive rock from the acapulcoite‐lodranite (AL) parent asteroid on the basis of the petrographic analysis of 5 small (<8.3 g) meteorite specimens from the Frontier Mountain ice field (Antarctica). Although these individual specimens may not be representative of the parent‐rock lithology due to their relatively large grain size, by putting together evidence from various thin sections and literature data we conclude that Frontier Mountain (FRO) 90011, FRO 93001, FRO 99030, and FRO 03001 are paired fragments of a medium‐ to coarse‐grained igneous rock which intrudes a lodranite and entrains xenoliths. The igneous matrix is composed of enstatite (Fs_{13.3 ± 0.4} Wo_{3.1 ± 0.2}), Cr‐rich augite (Fs_{6.1 ± 0.7} Wo_{42.3 ± 0.9}), and oligoclase (Ab_{80.5 ± 3.3} Or_{3.2 ± 0.6}). The lodranitic xenoliths show a fine‐grained (average grain size 488 ± 201 μm) granoblastic texture and consist of olivine Fa_{9.5 ± 0.4} and Fe,Ni metal and minor amounts of enstatite Fs_{12.7 ± 0.4} Wo_{1.8 ± 0.1}, troilite, chromite, schreibersite, and Ca‐phosphates. Crystals of the igneous matrix and lodranitic xenoliths are devoid of shock features down to the scanning electron microscope scale. From a petrogenetic point of view, the lack of shock evidence in the lodranitic xenoliths of all the studied samples favors the magmatic rather than the impact melting origin of this rock. FRO 95029 is an acapulcoite and represents a separate fall from the AL parent asteroid, i.e., it is not a different clast entrained by the FRO 90011, FRO 93001, FRO 99030, and FRO 03001 melt, as in genomict breccias common in the meteoritic record. The specimen‐to‐meteorite ratio for the AL meteorites so far found at Frontier Mountain is thus 2.5.     

Remelting of refractory inclusions in the chondrule‐forming regions: Evidence from chondrule‐bearing type C calcium‐aluminum‐rich inclusions from Allende

Abstract— We describe the mineralogy, petrology, oxygen, and magnesium isotope compositions of three coarse‐grained, igneous, anorthite‐rich (type C) Ca‐Al‐rich inclusions (CAIs) (ABC, TS26, and 93) that are associated with ferromagnesian chondrule‐like silicate materials from the CV carbonaceous chondrite Allende. The CAIs consist of lath‐shaped anorthite (An₉₉), Cr‐bearing Al‐Ti‐diopside (Al and Ti contents are highly variable), spinel, and highly åkermanitic and Na‐rich melilite (Åk_63–74, 0.4–0.6 wt% Na₂O). TS26 and 93 lack Wark‐Lovering rim layers; ABC is a CAI fragment missing the outermost part. The peripheral portions of TS26 and ABC are enriched in SiO₂ and depleted in TiO₂ and Al₂O₃ compared to their cores and contain relict ferromagnesian chondrule fragments composed of forsteritic olivine (Fa_6–8) and low‐Ca pyroxene/pigeonite (Fs₁Wo_1–9). The relict grains are corroded by Al‐Ti‐diopside of the host CAIs and surrounded by haloes of augite (Fs_0.5Wo_30–42). The outer portion of CAI 93 enriched in spinel is overgrown by coarse‐grained pigeonite (Fs_0.5–2Wo_5–17), augite (Fs_0.5Wo_38–42), and anorthitic plagioclase (An₈₄). Relict olivine and low‐Ca pyroxene/pigeonite in ABC and TS26, and the pigeonite‐augite rim around 93 are ¹⁶O‐poor (Δ17O ～ ?1‰ to ?8‰). Spinel and Al‐Ti‐diopside in cores of CAIs ABC, TS26, and 93 are ¹⁶O‐enriched (Δ17O down to ?20‰), whereas Al‐Ti‐diopside in the outer zones, as well as melilite and anorthite, are ¹⁶O‐depleted to various degrees (Δ17O = ?11‰ to 2‰). In contrast to typical Allende CAIs that have the canonical initial ²⁶Al/²⁷Al ratio of ～5 × 10^?5 ABC, 93, and TS26 are ²⁶Al‐poor with (²⁶Al/²⁷Al)₀ ratios of (4.7 ± 1.4) × 10^?6 (1.5 ± 1.8) × 10^?6 <1.2 × 10^?6 respectively. We conclude that ABC, TS26, and 93 experienced remelting with addition of ferromagnesian chondrule silicates and incomplete oxygen isotopic exchange in an ¹⁶O‐poor gaseous reservoir, probably in the chondrule‐forming region. This melting episode could have reset the ²⁶Al‐²⁶Mg systematics of the host CAIs, suggesting it occurred ～2 Myr after formation of most CAIs. These observations and the common presence of relict CAIs inside chondrules suggest that CAIs predated formation of chondrules.     

High‐pressure phases in shock‐induced melt veins of the Umbarger L6 chondrite: Constraints of shock pressure

Abstract— We report a previously undocumented set of high‐pressure minerals in shock‐induced melt veins of the Umbarger L6 chondrite. High‐pressure minerals were identified with transmission electron microscopy (TEM) using selected area electron diffraction and energy‐dispersive X‐ray spectroscopy. Ringwoodite (Fa₃₀), akimotoite (En₁₁Fs₈₉), and augite (En₄₂Wo₃₃Fs₂₅) were found in the silicate matrix of the melt vein, representing the crystallization from a silicate melt during the shock pulse. Ringwoodite (Fa₂₇) and hollandite‐structured plagioclase were also found as polycrystalline aggregates in the melt vein, representing solid state transformation or melting with subsequent crystallization of entrained host rock fragments in the vein. In addition, Fe₂SiO₄‐spinel (Fa₆₆‐Fa₉₉) and stishovite crystallized from a FeO‐SiO₂‐rich zone in the melt vein, which formed by shock melting of FeO‐SiO₂‐rich material that had been altered and metasomatized before shock. Based on the pressure stabilities of the high‐pressure minerals, ringwoodite, akimotoite, and Ca‐clinopyroxene, the melt vein crystallized at approximately 18 GPa. The Fe₂SiO₄‐spinel + stishovite assemblage in the FeO‐SiO₂‐rich melts is consistent with crystallization of the melt vein matrix at the pressure up to 18 GPa. The crystallization pressure of ?18 GPa is much lower than the 45–90 GPa pressure one would conclude from the S6 shock effects in melt veins (Stöffler et al. 1991) and somewhat less than the 25–30 GPa inferred from S5 shock effects (Schmitt 2000) found in the bulk rock.     

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.     

The Antarctic achondrite,Grove Mountains 021663: An olivine‐rich winonaite

Abstract– The Grove Mountains (GRV) 021663 meteorite was collected from the Grove Mountains region of Antarctica. The meteorite is composed primarily of olivine (Fa_5.4), orthopyroxene (Fs_4.7Wo_3.0), chromian diopside (En_53.6Fs_2.4Wo₄₄), troilite, kamacite, and plagioclase (Ab_74.5Or₄An_21.5). Minor phases include schreibersite and K‐feldspar. The meteorite is highly weathered (W3) and weakly shocked (S2). We determine a whole rock oxygen isotopic composition of δ¹⁸O = 7.50‰, δ¹⁷O = 3.52‰. Comparisons of these data with other primitive achondrites have resulted in the reclassification of this meteorite as a member of the winonaite group. The occurrences of troilite, metal, and schreibersite in GRV 021663 indicate that these minerals were once completely molten. Euhedral inclusions of pyroxene within plagioclase further suggest that these may have crystallized from a silicate melt, while the depletion of plagioclase, metal, and troilite indicates that GRV 021663 could represent a residuum following partial melting on its parent asteroid. Trace element distributions in silicate minerals do not, however, confirm this scenario. As with other winonaite meteorites, the formation of GRV 021663 probably relates to brecciation and mixing of heterogeneous lithologies, followed by varying degrees of thermal metamorphism on the parent body asteroid. Peak metamorphic conditions may have resulted in localized partial melting of metal and silicate mineralogies, but our data are not conclusive.     

Petrology and geochemistry of Patuxent Range 91501, a clast‐poor impact melt from the L‐chondrite parent body and Lewis Cliff 88663, an L7 chondrite

Abstract— We have performed petrologic and geochemical studies of Patuxent Range (PAT) 91501 and Lewis Cliff (LEW) 88663. PAT 91501, originally classified as an L7 chondrite, is rather a unique, near total impact melt from the L‐chondrite parent body. Lewis Cliff 88663 was originally classified as an “achondrite (?)”, but we find that it is a very weakly shocked L7 chondrite. PAT 91501 is an unshocked, homogeneous, igneous‐textured ultramafic rock composed of euhedral to subhedral olivine, low‐Ca pyroxene, augite and chrome‐rich spinels with interstitial albitic plagioclase and minor silica‐alumina‐alkali‐rich glass. Only ～10% relic chondritic material is present. Olivine grains are homogeneous (Fa_25.2–26.8). Low‐Ca pyroxene (Wo_1.9–7.2En_71.9–78.2Fs_19.9–20.9) and augite (Wo_29.8–39.0En_49.2–55.3Fs_11.8–14.9) display a strong linear TiO₂‐Al₂O₃ correlation resulting from igneous fractionation. Plagioclase is variable in composition; Or_3.0–7.7Ab_79.8–84.1An_8.2–17.2.‐Chrome‐rich spinels are variable in composition and zoned from Cr‐rich cores to Ti‐Al‐rich rims. Some have evolved compositions with up to 7.9 wt% TiO₂. PAT 91501 bulk silicate has an L‐chondrite lithophile element composition except for depletions in Zn and Br. Siderophile and chalcophile elements are highly depleted due to sequestration in centimeter‐size metal‐troilite nodules. The minerals in LEW 88663 are more uniform in composition than those in PAT 91501. Olivine grains have low CaO and Cr₂O₃ contents similar to those in L5–6 chondrites. Pyroxenes have high TiO₂ contents with only a diffuse TiO₂‐Al₂O₃ correlation. Low‐Ca pyroxenes are less calcic (Wo_1.6–3.1En_76.5–77.0Fs_20.4–21.4), while augites (Wo_39.5–45.6En_46.8–51.1Fs_7.6–9.4) and plagioclases (Or_2.6–5.7Ab_74.1–83.1An_11.2–23.3) are more calcic. Spinels are homogeneous and compositionally similar to those in L6 chondrites. LEW 88663 has an L‐chondrite bulk composition for lithophile elements, and only slight depletions in siderophile and chalcophile elements that are plausibly due to weathering and/or sample heterogeneity.     

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.     

Petrology of silicate inclusions in the Sombrerete ungrouped iron meteorite: Implications for the origins of IIE‐type silicate‐bearing irons

Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo_1–4Fs_25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An_70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.     

Northwest Africa 4797: A strongly shocked ultramafic poikilitic shergottite related to compositionally intermediate Martian meteorites

Abstract– Northwest Africa (NWA) 4797 is an ultramafic Martian meteorite composed of olivine (40.3 vol%), pigeonite (22.2%), augite (11.9%), plagioclase (9.1%), vesicles (1.6%), and a shock vein (10.3%). Minor phases include chromite (3.4%), merrillite (0.8%), and magmatic inclusions (0.4%). Olivine and pyroxene compositions range from Fo_66–72,En_58–74Fs_19–28Wo_6–15, and En_46–60Fs_14–22Wo_34–40, respectively. The rock is texturally similar to “lherzolitic” shergottites. The oxygen fugacity was QFM?2.9 near the liquidus, increasing to QFM?1.7 as crystallization proceeded. Shock effects in olivine and pyroxene include strong mosaicism, grain boundary melting, local recrystallization, and pervasive fracturing. Shock heating has completely melted and vesiculated igneous plagioclase, which upon cooling has quench‐crystallized plagioclase microlites in glass. A mm‐size shock melt vein transects the rock, containing phosphoran olivine (Fo_69–79), pyroxene (En_44–51Fs_14–18Wo_30–42), and chromite in a groundmass of alkali‐rich glass containing iron sulfide spheres. Trace element analysis reveals that (1) REE in plagioclase and the shock melt vein mimics the whole rock pattern; and (2) the reconstructed NWA 4797 whole rock is slightly enriched in LREE relative to other intermediate ultramafic shergottites, attributable to local mobilization of melt by shock. The shock melt vein represents bulk melting of NWA 4797 injected during pressure release. Calculated oxygen fugacity for NWA 4797 indicates that oxygen fugacity is decoupled from incompatible element concentrations. This is attributed to subsolidus re‐equilibration. We propose an alternative nomenclature for “lherzolitic” shergottites that removes genetic connotations. NWA 4797 is classified as an ultramafic poikilitic shergottite with intermediate trace element characteristics.     

Petrology,geochemistry, and cosmic‐ray exposure age of Iherzolitic shergottite Northwest Africa 1950

Northwest Africa (NWA) 1950 is a new member of the lherzolitic shergottite clan of the Martian meteorites recently found in the Atlas Mountains. The petrological, mineralogical, and geochemical data are very close to those of the other known lherzolitic shergottites. The meteorite has a cumulate gabbroic texture and its mineralogy consists of olivine (Fo₆₆ to Fo₇₅), low and high‐Ca pyroxenes (En₇₈Fs₁₉Wo₂‐En₆₀Fs₂₆W₁₄; En₅₃Fs₁₆Wo₃₁‐En₄₅Fs₁₄Wo₄₁), and plagioclase (An₅₇Ab₄₁Or₁ to An₄₀Ab₅₇Or₃; entirely converted into maskelynite during intense shock metamorphism). Accessory minerals include phosphates (merrillite), chromite and spinels, sulfides, and a glass rich in potassium. The oxygen isotopic values lie on the fractional line defined by the other SNC meteorites (Δ¹⁷O = 0.312 %o). The composition of NWA 1950 is very similar to the other lherzolitic shergottites and suggests an origin from the same magmatic system, or at least crystallization from a close parental melt. Cosmogenic ages indicate an ejection age similar to those of the other lherzolitic shergottites. The intensity of the shock is similar to that observed in other shergottites, as shown by the occurrence of small melt pockets containing glass interwoven with stishovite.     

The Divnoe meteorite: Petrology,chemistry, oxygen isotopes and origin

Abstract— The Divnoe meteorite is an olivine-rich primitive achondrite with subchondritic chemistry and mineralogy. It has a granoblastic, coarse-grained, olivine groundmass (CGL: coarse-grained lithology) with relatively large pyroxene-plagioclase poikilitic patches (PP) and small fine-grained domains of an opaque-rich lithology (ORL). Both PP and ORL are inhomogeneously distributed and display reaction boundaries with the groundmass. Major silicates, olivine (Fa_20–28) and orthopyroxene (Fs_20–28 Wo_0.5–2.5), display systematic differences in composition between CGL and ORL as well as a complicated pattern of variations within CGL. Accessory plagioclase has low K content and displays regular igneous zoning with core compositions An_40–45 and rims An_32–37. The bulk chemical composition of Divnoe is similar to that of olivine-rich primitive achondrites, except for a depletion of incompatible elements and minor enrichment of refractory siderophiles. Oxygen isotope compositions for whole-rock and separated minerals from Divnoe fall in a narrow range, with mean δ¹⁸O = +4.91, δ¹⁷O = +2.24, and Δ¹⁷O = ?0.26 ± 0.11. The isotopic composition is not within the range of any previously recognized group but is very close to that of the brachinites. To understand the origin of Divnoe lithologies, partial melting and crystallization were modelled using starting compositions equal to that of Divnoe and some chondritic meteorites. It was found that the Divnoe composition could be derived from a chondritic source region by ～20 wt% partial melting at T ～ 1300 °C and log(fO₂) = IW-1.8, followed by ～60 wt% crystallization of the partial melt formed, and removal of the still-liquid portion of the partial melt. Removal of the last partial melt resulted in depletion of the Divnoe plagioclase in Na and K. In this scenario, CGL represents the residue of partial melting, and PP is a portion of the partial melt that crystallized in situ. The ORL was formed during the final stages of partial melting by reaction between gaseous sulfur and residual olivine in the source region. A prominent feature of Divnoe is fine μm-scale chemical variations within olivine grains, related to lamellar structures the olivines display. The origin of these structures is not known.     

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

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

Transmission electron microscope texture and crystal chemistry of coexisting ortho- and clinopyroxene in the Antarctic ureilite Frontier Mountain 90054: Implications for thermal history

Abstract— Frontier Mountain (FRO) 90054, from Antarctica, is a rare clino- and orthopyroxene-bearing ureilite with a coarse equigranular oriented texture (grains up to 3 mm); it is classified as a low-shock Ca-rich type. The crystal chemistry of its clinopyroxene (Wo_39.3En_54.6Fs_6.1), orthopyroxene (En_{84 2}Fs₁₁Wo_4.8) and olivine (Fa_12.6Fo_86.9) was investigated by single-crystal x-ray structural refinements and transmission electron microscope (TEM) observations to obtain data on the evolutionary history of the parent body. The M1 octahedron and unit cell volumes of the orthopyroxene and clinopyroxene are consistent with low-pressure crystallization. The closure temperatures for intracrystalline Mg-Fe²⁺ ordering yielded values of 674 °C and 804 °C for opx and 596 °C for cpx, which indicate high-temperature equilibration and fast cooling. Trasmission electron microscope investigations were performed on clinopyroxene, orthopyroxene and pigeonite. The (100) twin lamellae in the clinopyroxene and intergrowth of clino- and orthoenstatite lamellae in orthopyroxene most probably originated by deformation. Exsolution was not observed in any of the phases, which suggests rapid cooling. Analysis by TEM also revealed interstitial Na-rich glass and pigeonite with sharp h + k odd reflections and rare stacking faults parallel to (100). Textural and crystal chemical data, obtained by TEM, indicated rapid cooling that was probably due to fast radiative heat loss as a result of the disintegration of the parent body into small fragments, which subsequently reassembled into a larger body. One or more collisional events caused fine-scale stacking faults and partial melting.     

Mineralogical composition of (25143) Itokawa 1998 SF36 from visible and near‐infrared reflectance spectroscopy: Evidence for partial melting

Abstract— –In March 2001, asteroid (25143) Itokawa, the target of the Japanese Hayabusa spacecraft mission, was in a favorable viewing geometry for ground‐based telescopic study. Visible/near‐infrared (VNIR) spectra (～～0.48 to 0.9 μm) obtained on March 24, 26, and 27 UT, and near‐infrared (NIR) spectra (～～0.75 to 2.5 μm) obtained on March 10, 11, 12, 23, and 24 UT collectively show absorption features centered near 1.0 and 2.0 μm, which are indicative of olivine and pyroxene. Analyses of these absorption features indicate an abundance ratio of olivine to pyroxene of approximately 75:25 ± 5, respectively, with no significant variation in the relative abundance of these minerals across its surface on a regional scale. The band center positions indicate that the mean pyroxene chemistry is ～～Wo_{14 ± 5}Fs_{43 ± 5}. There appear to be at least two pyroxene components: primarily a low‐Ca orthopyroxene accompanied by a spectrally significant (～～15–20%) high Fe‐rich pigeonite phase. The mean pyroxene composition is significantly more Fe‐rich than the Fs_14–26 range found in ordinary chondrites. These pyroxene compositions are suggestive of phases crystallized from partial melts. This would indicate that the parent body of (25143) Itokawa reached temperatures sufficient to initiate partial melting (～～1050 to 1250 °C), but that it did not attain the degree of melting required for significant melt mobilization and efficient segregation of the basaltic melt component from the unmelted residual olivine portion. Itokawa's spectral band parameters place it near the S(III)/S(IV) boundary, but within the S(III) taxonomic field. In meteoritic nomenclature, Itokawa would be most analogous to an olivine‐rich primitive achondrite. Alternatively, if the high Fs value is not related to partial melting, then Itokawa could also represent a rare atypical LL chondrite, or a previously unsampled oxidized Fe‐rich chondritic‐like assemblage.     

NWA 1152 and Sahara 00182: New primitive carbonaceous chondrites with affinities to the CR and CV groups

Abstract— We have investigated the mineralogy, petrography, bulk chemistry, and light element isotope composition of the ungrouped chondrites North West Africa (NWA) 1152 and Sahara 00182. NWA 1152 contains predominantly type 1 porphyritic olivine (PO) and porphyritic olivinepyroxene (POP) chondrules. Chondrule silicates are magnesium‐rich (Fo_{98.8 ± 1.2}, n = 36; Fs_{2.3 ± 2.1} Wo_{1.2 ± 0.3}, n = 23). Matrix comprises ?40 vol% of the sample and is composed of a micron sized silicate groundmass with larger silicate, sulfide, magnetite, and Fe‐Ni metal (Ni ?50 wt%) grains. Phyllosilicates were not observed in the matrix. Refractory inclusions are rare (0.3 vol%) and are spinel pyroxene aggregates or amoeboid olivine aggregates; melilite is absent from the refractory inclusions. Sahara 00182 contains predominantly type 1 PO chondrules, POP chondrules are less common. Most chondrules contain blebs of, and are often rimmed with, Fe‐Ni metal and sulfide. Chondrule phenocrysts are magnesium‐rich (Fo_{92.2 ± 0.6}, n = 129; Fs_{4.4 ± 1.8} Wo_{1.3 ± 1.1}, n = 16). Matrix comprises ?30 vol% of the meteorite and is predominantly sub‐micron silicates, with rare larger silicate gains. Matrix Fe‐Ni metal (mean Ni = 5.8 wt%) and sulfide grains are up to mm scale. No phyllosilicates were observed in the matrix. Refractory inclusions are rare (1.1 vol%) and melilite is absent. The oxygen isotope composition of NWA 1152 falls within the range of the CV chondrites with δ¹⁷O = ?3.43%0 δ¹⁸O = 0.70%0 and is similar to Sahara 00182, δ¹⁷O = ?3.89%0, δ¹⁸O = ?0.19%0 (Grossman and Zipfel 2001). Based on mineralogical and petrographic characteristics, we suggest NWA 1152 and Sahara 00182 show many similarities with the CR chondrites, however, oxygen isotopes suggest affinity with the CVs. Thus, neither sample can be assigned to any of the currently known carbonaceous chondrite groups based on traditionally recognized characteristics. Both samples demonstrate the complexity of inter‐ and intra‐group relationships of the carbonaceous chondrites. Whatever their classification, N WA 1152 and Sahara 00182 represent a source of relatively pristine solar system material.     

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

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

Fe‐bearing phases in a ureilite fragment from the asteroid 2008 TC3 (= Almahata Sitta meteorites): A combined Mössbauer spectroscopy and X‐ray diffraction study

The iron‐bearing phases in a ureilite fragment (AS#051) from the Almahata Sitta meteorite are studied using Mössbauer spectroscopy, X‐ray diffraction (XRD), and electron microprobe analysis (EMPA). AS#051 has a typical ureilite texture of medium‐ to coarse‐grained silicates (olivine, orthopyroxene, and pigeonite) with minor opaques (Fe‐Ni metal, troilite, and graphite). The silicate compositions, determined by EMPA, are homogeneous: olivine (Fo_90.2), orthopyroxene (En_86.3Fs_8.6Wo_5.1), and pigeonite (En_81.6Fs_8.9Wo_9.5), and are similar to those of magnesian ureilites. The modal abundance of mineral phases was determined by Rietveld refinement of the powder XRD data. The Mössbauer spectra at 295 K and 78 K are composed of two sharp well‐defined paramagnetic doublets superimposed on a well‐resolved magnetic sextet and other weak absorption features. The two paramagnetic doublets are assigned to olivine and pyroxene (orthopyroxene and pigeonite), and the ferromagnetic sextet to kamacite (magnetic hyperfine field ≈ 33.2 T), in agreement with the XRD characterization. The Mössbauer results also show the presence of small amounts of troilite (FeS) and cohenite ([Fe,Ni,Co]₃C). Using the Mössbauer data, the relative abundance of each Fe‐bearing phase is determined and compared with the results obtained by XRD.     

METEOMOD: A numerical model for the calculation of melting-crystallization relationships in meteoritic igneous systems

Abstract— The METEOMOD model is a computer program designed to calculate melting-crystallization relationships in igneous systems compositionally similar to ordinary chondrites and basaltic achondrites. The core of METEOMOD is a set of empirically calibrated equations, called geothermometers, which describe equilibria between silicate melt and minerals such as olivine, orthopyroxene, pigeonite, augite, plagioclase, and metallic Fe in terms of pressure, temperature, and liquid compositions. The silicate mineral geothermometers are calibrated from a database containing the compositions of melts and minerals produced in melting experiments on 113 meteoritic and 141 synthetic systems. The metallic iron-silicate melt geothermometer is calibrated from a database of 396 melting experiments. The Meteorite Melting Model or METEOMOD calculates crystallization temperatures and contents of major end members in mineral solid solutions with accuracies of ±10–15 °C and ±1–2 mol%, respectively. Input parameters for the program are (1) increment in crystallization degree; (2) one of 12f_O2 buffers routinely used in petrology; (3) shift from the buffer in log units, if any; (4) a choice of equilibrium or fractional crystallization trajectory; (5) terminal crystallization degree; (6) contents of ten major elements in wt%; (7) a set of minor and trace elements in parts per million; (8) the number of initial compositions to be modeled in a single computation run. The output consists of a series of tables that list equilibrium temperatures, O fugacities, and proportions of melt and minerals and their compositions, as a function of the degree of crystallization. The results of application of METEOMOD to modeling of melting-crystallization of the St. Severin LL chondrite are compared with the experimental data of Jurewicz et al. (1995).     

Petrogenesis of Grove Mountains 020090: An enriched “lherzolitic” shergottite

Grove Mountains (GRV) 020090 is a “lherzolitic” shergottite found in the Grove Mountains, Antarctica. It exhibits two distinct textures: poikilitic and nonpoikilitic. In poikilitic areas, large pyroxene oikocrysts enclose subhedral olivine and chromite chadacrysts. Pyroxene oikocrysts are zoned from pigeonite cores to augite rims. In nonpoikilitic areas, olivine, pyroxene, and interstitial maskelynite occur as major phases, and minor phases include chromite and merrillite. Compared with typical “lherzolitic” shergottites, GRV 020090 contains a distinctly higher abundance of maskelynite (19 vol%). Olivine and pyroxene are more ferroan (Fa_28–40, En_57–72Fs_24–31Wo_4–14 and En_46–53Fs_17–21Wo_26–35), and maskelynite is more alkali‐rich (Ab_43–65Or_2–7). The major phases, whole‐rock (estimated) and fusion crust of GRV 020090, are relatively enriched in light rare earth elements (LREE), similar to those of the geochemically enriched basaltic shergottites, but distinct from those of LREE‐depleted “lherzolitic” shergottites. Combined with a high oxygen fugacity of log fO₂ = QFM ? 1.41 ± 0.04 (relative to the quartz‐fayalite‐magnetite buffer), it is clear that GRV 020090 sampled from an oxidized and enriched mantle reservoir similar to those of other enriched shergottites. The calculated REE abundances and patterns of the melts in equilibrium with the cores of major phases are parallel to but higher than that of the whole rock, suggesting that GRV 020090 originated from a single parent magma and experienced progressive fractional crystallization in a closed system. The crystallization age recorded by baddeleyite is 192 ± 10 (2σ) Ma, consistent with the young internal isochron ages of enriched shergottites. Baddeleyite dating results further demonstrated that the young ages, rather than ancient ages (>4 Ga), appear to represent the crystallization of Martian surface lava flow. GRV 020090 shares many similarities with Roberts Massif (RBT) 04261/2, the first enriched “lherzolitic” shergottite. Detailed comparisons suggest that these two rocks are petrologically and geochemically closely related, and probably launch paired.     

Watson: A new link in the HE iron chain

Abstract— Watson, which was found in 1972 in South Australia, contains the largest single silicate rock mass seen in any known iron meteorite. A comprehensive study has been completed on this unusual meteorite: petrography, metallography, analyses of the silicate inclusion (whole rock chemical analysis, INAA, RNAA, noble gases, and oxygen isotope analysis) and mineral compositions (by electron microprobe and ion microprobe). The whole rock has a composition of an H-chondrite minus the normal H-group metal and troilite content. The oxygen isotope composition is that of the silicates in the HE iron meteorites and lies along an oxygen isotope fractionation line with the H-group chondrites. Trace elements in the metal confirm Watson is a new HE iron. Whole rock Watson silicate shows an enrichment in K and P (each ～2X H-chondrites). The silicate inclusion has a highly equilibrated igneous (peridotite-like) texture with olivine largely poikilitic within low-Ca pyroxene: olivine (Fa₂₀), opx (Fs₁₇Wo₃), capx (Fs₉Wo₄₁) (with very fine exsolution lamellae), antiperthite feldspar (An_1–Or₅) with <1 μm exsolution lamellae (An_1–3Or_>40), shocked feldspar with altered stoichiometry, minor whitlockite (also a poorly characterized interstitial phosphate-rich phase) and chromite, and only traces of metal and troilite. The individual silicate minerals have normal chondritic REE patterns, but whitlockite has a remarkable REE pattern. It is very enriched in light REE (La is 720X C1, and Lu is 90X C1, as opposed to usual chonditic values of ～300X and 100–150X, respectively) with a negative Eu anomaly. The enrichment of whole rock K is expressed both in an unusually high mean modal Or content of the feldspar, Or₁₃, and in the presence of antiperthite. Whole rock trace element data for the silicate mass support the petrography. Watson silicate was an H-chondrite engulfed by metal and melted at > 1550 °C. A flat refractory lithophile and flat REE pattern (at ～1x average H-chondrites) indicate that melting took place in a relatively closed system. Immiscible metal and sulfide were occluded into the surrounding metal host. Below 1100 °C, the average cooling rate is estimated to have been ～1000 °C/Ma; Widmanstätten structure formed, any igneous zoning in the silicates was equilibrated, and feldspar and pyroxene exsolution took place. Cooling to below 300 °C was completed by 3.5 Ga B. P. At 8 Ma, a shock event took place causing some severe metal deformation and forming local melt pockets of schreibersite/metal. This event likely caused the release of Watson into interplanetary space. The time of this event, 8Ma, corresponds to the peak frequency of exposure ages of the H-chondrites. This further confirms the link between HE irons and the H-chondrites, a relationship already indicated by their common oxygen isotope source. Watson metal structures are very similar to those in Kodaikanal. Watson, Kodaikanal and Netschaëvo form the young group of HE meteorites (ages 3.7 ± 0.2 Ga). They appear to represent steps in a chain of events that must have taken place repeatedly on the HE parent body or bodies from which they came: chondrite engulfed in metal (Netschaëvo); chondrite melted within metal (Watson); and finally melted silicate undergoing strong fractionation with the fractionated material emplaced as globules within metal (Kodaikanal). Watson fills an important gap in understanding the sequence of events that took place in the evolution of the IIE-H parent body(ies). This association of H-chondrite with HE metal suggests a surface, or near surface process-a suggestion made by several other researchers.