Silica as a shock index in shergottites: A cathodoluminescence study

Abstract— Silica in shergottites is a minor phase of great significance. Determining its structural state as either silica glass, quartz, cristobalite, tridymite, coesite, stishovite, or post‐stishovite could provide informations about their shock history. The purpose of this work is to assess the shock intensity in shergottites using two spectroscopic methods. On a conventional polished section, a scanning electron microscope (SEM) enables us to study the cathodoluminescence (CL) of silica at variable magnification. The results were crosschecked by systematic Raman spectroscopy of the selected areas. CL spectra differ substantially from one another and enable separating stishovite, high and low pressure silica glass, quartz, and cristobalite. We studied a set of five shergottites: Northwest Africa (NWA) 480, NWA 856, Zagami, Shergotty, and Los Angeles. Stishovite is common in Shergotty, Zagami, NWA 856, and NWA 480 and absent in the studied section of Los Angeles. High‐pressure glass is very common, particularly in close association with stishovite. According to the textural relationship, it may be a product of the retromorphosis (amorphization during decompression) of stishovite. Large stishovite areas result from the transformation of preexisting low‐pressure silica crystals, while needles result from the high‐pressure transformation of pyroxene to glass (melt) and silica. In the latter case, they are found in melt pockets and represent a small fraction of areas of overall pyroxene composition. Needles exhibit square sections of about 1 μm. Silica spots identical to those described previously as post‐stishovite are found in Shergotty, Zagami, NWA 480, and NWA 856. At present, the spectroscopic distinction of post‐stishovite from stishovite is difficult. Post‐stishovite is destroyed under the Raman beam, and CL spectra are possible mixtures of several phases (e.g., glass and post‐stishovite). It is concluded that the shock intensity is highly heterogeneous, and the pressure probably exceeded 60 GPa in all shergottites studied here.     

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.     

Northwest Africa 10414, a pigeonite cumulate shergottite

Northwest Africa (NWA) 10414 is an unusual shergottite with a cumulate texture. It contains 73% coarse prismatic pigeonite, plus 18% interstitial maskelynite, 2% Si‐rich mesostasis, 2% merrillite, and minor chromite‐ulvöspinel. It contains no olivine, and only ~3% augite. Phase compositions are pigeonite (En_68‐43Fs_27‐48Wo_5‐15) and maskelynite An_~54‐36, more sodic than most maskelynite in shergottites. Chromite‐ulvöspinel composition plots between the earliest and most fractionated spinel‐group minerals in olivine‐phyric shergottites. NWA 10414 mineralogically resembles the contact facies between Elephant Moraine 79001 lithologic units A and B, with abundant pigeonite phenocrysts, though it is coarser grained. Its most Mg‐rich pigeonite also has a similar composition to the earliest crystallized pyroxenes in several other shergottites, including Shergotty. The Shergotty intercumulus liquid composition crystallizes pigeonite with a similar composition range to NWA 10414 pigeonite, using PETROLOG. Olivine‐phyric shergottite NWA 6234, with a pure magma composition, produces an even better match to this pigeonite composition range, after olivine crystallization. These observations suggest that after the accumulation of olivine from an olivine‐phyric shergottite magma, the daughter liquid could precipitate pigeonite locally to form this pigeonite cumulate, before the crystallization of overlying liquid as a normal basaltic shergottite.     

The Ksar Ghilane 002 shergottite—The 100th registered Martian meteorite fragment

We report on the discovery of a new shergottite from Tunisia, Ksar Ghilane (KG) 002. This single stone, weighing 538 g, is a coarse‐grained basaltic shergottite, mainly composed of maskelynitized plagioclase (approximately 52 vol%) and pyroxene (approximately 37 vol%). It also contains Fe‐rich olivine (approximately 4.5 vol%), large Ca‐phosphates, including both merrillites and Cl‐apatites (approximately 3.4 vol%), minor amounts of silica or SiO₂‐normative K‐rich glass, pyrrhotite, Ti‐magnetite, ilmenite, and accessory baddeleyite. The largest crystals of pyroxene and plagioclase reach sizes of approximately 4 to 5 mm. Pyroxenes (Fs_26–96En_5–50Wo_2–41). They typically range from cores of about Fs₂₉En₄₁Wo₃₀ to rims of about Fs₆₈En₁₄Wo₁₇. Maskelynite is Ab_41–49An_39–58Or_1–7 in composition, but some can be as anorthitic as An₉₃. Olivine (Fa_91–96) occurs mainly within symplectitic intergrowths, in paragenesis with ilmenite, or at neighboring areas of symplectites. KG 002 is heavily shocked (S5) as indicated by mosaic extinction of pyroxenes, maskelynitized plagioclase, the occurrence of localized shock melt glass pockets, and low radiogenic He concentration. Oxygen isotopes confirm that it is a normal member of the SNC suite. KG 002 is slightly depleted in LREE and shows a positive Eu anomaly, providing evidence for complex magma genesis and mantle processes on Mars. Noble gases with a composition thought to be characteristic for Martian interior is a dominant component. Measurements of ¹⁰Be, ²⁶Al, and ⁵³Mn and comparison with Monte Carlo calculations of production rates indicate that KG 002 has been exposed to cosmic rays most likely as a single meteoroid body of 35–65 cm radius. KG 002 strongly resembles Los Angeles and NWA 2800 basaltic shergottites in element composition, petrography, and mineral chemistry, suggesting a possible launch‐pairing. The similar CRE ages of KG 002 and Los Angeles may suggest an ejection event at approximately 3.0 Ma.     

Petrology and chemistry of the basaltic shergottite North West Africa 480

Abstract— North West Africa (NWA) 480 is a new martian meteorite of 28 g found in the Moroccan Sahara in November 2000. It consists mainly of large gray pyroxene crystals (the largest grains are up to 5 mm in length) and plagioclase converted to maskelynite. Excluding the melt pocket areas, modal analyses indicate the following mineral proportions: 72 vol% pyroxenes extensively zoned, 25% maskelynite, 1% phosphates (merrillite and chlorapatite), 1% opaque oxides (ilmenite, ulvöspinel and chromite) and sulfides, and 1% others such as silica and fayalite. The compositional trend of NWA 480 pyroxenes is similar to that of Queen Alexandra Range (QUE) 94201 but in NWA 480 the pyroxene cores are more Mg‐rich (En₇₇‐En₆₅). Maskelynites display a limited zoning (An_42–50Ab_54‐48Or_2–4). Our observations suggest that NWA 480 formed from a melt with a low nuclei density at a slow cooling rate. The texture was achieved via a single‐stage cooling where pyroxenes grew continuously. A similar model was previously proposed for QUE 94201 by McSween et al. (1996). NWA 480 is an Al‐poor ferroan basaltic rock and resembles Zagami or Shergotty for major elements and compatible trace element abundances. The bulk rock analysis for oxygen isotopes yields Δ¹⁷O = +0.42%, a value in agreement at the high margin, with those measured on other shergottites (Clayton and Mayeda, 1996; Romanek et al., 1998; Franchi et al., 1999). Its CI‐normalized rare earth element pattern is similar to those of peridotitic shergottites such as Allan Hills (ALH)A77005, suggesting that these shergottites shared a similar parent liquid, or at least the same mantle source.     

Petrogenesis of basaltic shergottite Northwest Africa 8657: Implications for fO2 correlations and element redistribution during shock melting in shergottites

Northwest Africa (NWA) 8657 is an incompatible trace element-enriched, low-Al basaltic shergottite, similar in texture and chemistry to Shergotty, Zagami, and NWA 5298. It is composed of zoned pyroxene, maskelynite, merrillite, and Ti-oxide minerals with minor apatite, silica, and pyrrhotite. Pyroxene grains are characterized by patchy zoning, with pigeonite or augite cores zoned to Fe-rich pigeonite mantles. The cores have rounded morphologies and irregular margins. Combined with the low Ti/Al of the cores, the morphology and chemistry of the pyroxene grains are consistent with initial crystallization at depth (30–70 km) followed by partial resorption en route to the surface. Enriched rare earth element (REE) equilibrium melt compositions and calculated oxygen fugacities (fO₂) conditions for pigeonite cores indicate that the original parent melts were enriched shergottite magmas that staged in chambers at depth within the Martian crust. NWA 8657 does not represent a liquid but rather entrained a proportion of pyroxene crystals from magma chambers where fractional crystallization was occurring at depth. Variation between fO₂ and bulk-rock (La/Yb)_N of the enriched and intermediate shergottites suggests that oxidation conditions and degree of incompatible element enrichment in the source may not be correlated, as thought previously. Shock melt pockets are characterized by an absence of phosphates and oxide minerals. It is likely that these phases were melted during shock. REEs were redistributed during this process into maskelynite and to a lesser extent the shock melt; however, the overall normalized REE profile of the shock melt is like that of the bulk-rock, but at lower absolute concentrations. Overall, shock melting has had a significant effect on the mineralogy of NWA 8657, especially the distribution of phosphates, which may be significant for geochronological applications of this meteorite and other Martian meteorites with extensive shock melt.     

Sayh al Uhaymir 094: A new martian meteorite from the Oman desert

Abstract— Sayhal Uhaymir (SaU) 094 is a 223.3 g, partially crusted, strongly to very strongly shocked melanocratic olivine-porphyric rock of the shergottite group showing a microgabbroic texture. The rock consists of pyroxene (52.0–58.2 vol%)—dominantly prismatic pigeonite (En_60–68Fs_20–27Wo^7–9) associated with minor augite (En_46–49Fs_15–16Wo_28–31)—brown (shock-oxidized) olivine (Fo_65–69; 22.1–31%), completely isotropic interstitial plagioclase glass (maskelynite; An_50–64Or_0.3-0.9; 8.6–13.0%), chromite and titanian magnesian chromite (0.9-1.0%), traces of ilmenite (Ilm_80–86), pyrrhotite (Fe_92–100; 0.1-0.2%), merrillite (<<0.1%), and pockets (4.8-6.7%) consisting of green basaltic to basaltic andesitic shock glass that is partially devitrified into a brown to black product along boundaries with the primary minerals. The average maximum dimensions of minerals are: olivine (1.5 mm), pyroxene (0.3 mm) and maskelynite (0.3 mm). Primary melt inclusions in olivine and chromite are common and account for 0.1-0.6% of the rock. X-ray tomography revealed that the specimen contains ˜0.4 vol% of shock-melt associated vesicles, up to 3 mm in size, which show a preferred orientation. Fluidization of the maskelynite, melting and recrystallization of pyroxene, olivine and pyrrhotite indicate shock stage S6. Minor terrestrial weathering resulted in calcite-veining and minor oxidation of sulfides. The meteorite is interpreted as paired with SaU 005/008/051. The modal composition is similar to Dar al Gani 476/489/670/735/876, with the exception that neither mesostasis nor titanomagnetite nor apatite are present and that all phases show little zonation. The restricted mineral composition, predominance of chromite among the oxides, and abundance of olivine indicate affinities to the lherzolitic shergottites.     

Mineralogy of Antarctic basaltic shergottite Queen Alexandra Range 94201: Similarities to Elephant Moraine A79001 (Lithology B) martian meteorite

Abstract— Antarctic meteorite QUE 94201 is a new basaltic shergottite that is mainly composed of subequal amounts of maskelynite and pyroxenes (pigeonite and augite) plus abundant merrillite and accessory phases. It also contains impact melt. Complex zoning patterns in QUE 94201 pyroxenes revealed by elemental map analyses using an electron microprobe suggest a crystallization sequence from Mg-rich pigeonite (En₆₂Fss₃₀Wo_g) to extremely Fe-rich pigeonite (En₅Fs₈₁Wo₁₄) via {110} Mg-rich augite bands (En₄₄Fs₂₀Wo₃₆) in a single crystal. These textures, along with the abundant plagioclase (maskelynite), indicates single-stage rapid cooling (>5 °C/year) of this rock from a supercooled magma. Transition from Mg-rich augite to Fe-rich pigeonite reflects the onset of plagioclase crystallization. Enrichment of late-stage phases in QUE 94201 implies crystallization from an evolved magma and suggests a different parent magma composition from the other basaltic shergottites. Lithology B of EETA79001 basaltic shergottite contains pyroxenes that show complex zoning with augite bands similar to those in QUE 94201 pyroxene, which suggests similar one-stage rapid cooling. Lithology B of EETA79001 also resembles QUE 94201 in its coarse-grained texture of silicates and its high abundance of maskelynite, although QUE 94201 probably crystallized from a more fractionated magma. We also note that some Apollo lunar mare basalts (e.g., 12020 and 12021) have similar mineralogy and petrology to QUE 94201, especially in pyroxene zoning. All these basaltic rocks with complex pyroxene zoning suggest rapid metastable crystallization from supercooled magmas.     

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.     

Pervasive shock melting at >65 GPa in a Martian basalt,the shergottite Northwest Africa 14672

Shergottites have provided abundant information on the volcanic and impact history of Mars. Northwest Africa (NWA) 14672 contributes to both of these aspects. It is a vesicular ophitic depleted olivine–phyric shergottite, with average plagioclase An₆₁Ab₃₉Or_0.2. It is highly ferroan, with pigeonite compositions En_49-25Fs_41-61Wo_10-14 like those of basaltic shergottites, for example, NWA 12335. Olivine (Fo_53-15) has discrete ferroan overgrowths, more ferroan when in contact with plagioclase than when enclosed by pyroxene. The pyroxene (a continuum of augite, subcalcic augite, and pigeonite) is patchy, with ragged “cores” enveloped or invaded by ferroan pyroxene. Magma mixing may be responsible for capture of olivine and formation of pyroxene mantles. The plagioclase is maskelynite-like in appearance, but the original laths were (congruently) melted and the melt partly crystallized as fine dendrites. Most of the 14% vesicles occur within plagioclase. Olivine, pyroxene, and ilmenite occur in part as fine aggregates crystallized after congruent melting with limited subsequent liquid mixing. There are two fine-grained melt components, barred plagioclase with interstitial Fe-bearing phases, and glass with olivine dendrites, derived by melting of mainly plagioclase and mainly pyroxene, respectively. Rare silica particles contain coesite and/or quartz, and silica glass. The rock has experienced >50% melting, compatible with peak pressure >~65 GPa. It is the most highly shocked shergottite so far, at shock stage S6/7. It may belong to the group of depleted shergottites ejected at ~1 Myr from Tooting Crater.     

Petrogenesis of the Northwest Africa 4898 high‐Al mare basalt

Northwest Africa (NWA) 4898 is the only low‐Ti, high‐Al basaltic lunar meteorite yet recognized. It predominantly consists of pyroxene (53.8 vol%) and plagioclase (38.6 vol%). Pyroxene has a wide range of compositions (En_12–62Fs_25–62Wo_11–36), which display a continuous trend from Mg‐rich cores toward Ca‐rich mantles and then to Fe‐rich rims. Plagioclase has relatively restricted compositions (An_87–96Or_0–1Ab_4–13), and was transformed to maskelynite. The REE zoning of all silicate minerals was not significantly modified by shock metamorphism and weathering. Relatively large (up to 1 mm) olivine phenocrysts have homogenous inner parts with Fo ~74 and sharply decrease to 64 within the thin out rims (~30 μm in width). Four types of inclusions with a variety of textures and modal mineralogy were identified in olivine phenocrysts. The contrasting morphologies of these inclusions and the chemical zoning of olivine phenocrysts suggest NWA 4898 underwent at least two stages of crystallization. The aluminous chromite in NWA 4898 reveals that its high alumina character was inherited from the parental magma, rather than by fractional crystallization. The mineral chemistry and major element compositions of NWA 4898 are different from those of 12038 and Luna 16 basalts, but resemble those of Apollo 14 high‐Al basalts. However, the trace element compositions demonstrate that NWA 4898 and Apollo 14 high‐Al basalts could not have been derived from the same mantle source. REE compositions of its parental magma indicate that NWA 4898 probably originated from a unique depleted mantle source that has not been sampled yet. Unlike Apollo 14 high‐Al basalts, which assimilated KREEPy materials during their formation, NWA 4898 could have formed by closed‐system fractional crystallization.     

Mineralogy and petrology of the Dar al Gani 476 martian meteorite: Implications for its cooling history and relationship to other shergottites

Abstract— Dar al Gani 476, the 13th martian meteorite, was recovered from the Sahara in 1998. It is a basaltic shergottitic rock composed of olivine megacrysts reaching 5 mm (24 vol%) set in a finegrained groundmass of pyroxene (59 vol%) and maskelynitized plagioclase (12 vol%) with minor amounts of accessory phases (spinel, merrillite, ilmenite). Dar al Gani 476 is similar to lithology A of Elephant Moraine A79001 (EETA79001) in petrography and mineralogy, but is distinct in several aspects. Low‐Ca pyroxenes in the Dar al Gani 476 groundmass are more magnesian (En₇₆Fs₂₁ Wo₃～En₅₈Fs₃₀Wo₁₂) than those in lithology A of EETA79001 (En₇₃Fs₂₂Wo₅～En₄₅Fs₄₃Wo₁₂), rather similar to pyroxenes in lherzolitic martian meteorites (En₇₆Fs₂₁ Wo₃～En₆₃Fs₂₂Wo₁₅). Dar al Gani 476 olivine is less magnesian and shows a narrower compositional range (Fo_76‐58) than EETA79001 olivine (Fo_81‐53), and is also similar to olivines in lherzolitic martian meteorites (Fo_74‐65). The orthopyroxene‐olivine‐chromite xenolith typical in the lithology A of EETA79001 is absent in Dar al Gani 476. It seems that Dar al Gani 476 crystallized from a slightly more primitive mafic magma than lithology A of EETA79001 and several phases (olivine, pyroxene, chromite, and ilmenite) in Dar al Gani 476 may have petrogenetic similarities to those of lherzolitic martian meteorites. Olivine megacrysts in Dar al Gani 476 are in disequilibrium with the bulk composition. The presence of fractured olivine grains in which the most Mg‐rich parts are in contact with the groundmass suggests that little diffusive modification of original olivine compositions occurred during cooling. This observation enabled us to estimate the cooling rates of Dar al Gani 476 and EETA79001 olivines, giving similar cooling rates of 0.03‐3 °C/h for Dar al Gani 476 and 0.05‐5 °C/h for EETA79001. This suggests that they were cooled near the surface (burial depth shallower than about 3 m at most), probably in lava flows during crystallization of groundmass. As is proposed for lithology A of EETA79001, it may be possible to consider that Dar al Gani 476 has an impact melt origin, a mixture of martian lherzolite and other martian rock (Queen Alexandra Range 94201, nakhlites?).     

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.     

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.     

Magmatic cristobalite and quartz in the NWA 856 Martian meteorite

Abstract— Silica‐rich late‐stage crystallization pockets in the Martian meteorite Northwest Africa (NWA) 856 were investigated by transmission electron microscopy (TEM). The pockets occur as wedges between maskelynite laths or between maskelynite and pyroxene. They consist of elongated grains of cristobalite and quartz embedded in a silica‐rich glass. Interstitial to the amorphous phase and silica minerals, a number of small accessory minerals have been identified, typical for late‐stage crystallization products. They are ilmenite, tranquillityite, fayalite, troilite, baddeleyite, apatite, and chloroapatite. Cristobalite and quartz are shocked, as revealed by the occurrence of numerous amorphous lamellae. This assemblage suggests metastable dendritic crystallization under hydrous conditions. Cristobalite crystallization was probably facilitated by the presence of impurities such as Na or H₂O. Our observations show that silica minerals can be formed under magmatic conditions on Mars.     

Localized shock melting in lherzolitic shergottite Northwest Africa 1950: Comparison with Allan Hills 77005

Abstract— The lherzolitic Martian meteorite Northwest Africa (NWA) 1950 consists of two distinct zones: 1) low‐Ca pyroxene poikilically enclosing cumulate olivine (Fo_70–75) and chromite, and 2) areas interstitial to the oikocrysts comprised of maskelynite, low‐ and high‐Ca pyroxene, cumulate olivine (Fo_68–71) and chromite. Shock metamorphic effects, most likely associated with ejection from the Martian subsurface by large‐scale impact, include mechanical deformation of host rock olivine and pyroxene, transformation of plagioclase to maskelynite, and localized melting (pockets and veins). These shock effects indicate that NWA 1950 experienced an equilibration shock pressure of 35–45 GPa. Large (millimeter‐size) melt pockets have crystallized magnesian olivine (Fo_78–87) and chromite, embedded in an Fe‐rich, Al‐poor basaltic to picro‐basaltic glass. Within the melt pockets strong thermal gradients (minimum 1 °C/μm) existed at the onset of crystallization, giving rise to a heterogeneous distribution of nucleation sites, resulting in gradational textures of olivine and chromite. Dendritic and skeletal olivine, crystallized in the melt pocket center, has a nucleation density (1.0 × 10³ crystals/mm²) that is two orders of magnitude lower than olivine euhedra near the melt margin (1.6 × 10⁵ crystals/mm²). Based on petrography and minor element abundances, melt pocket formation occurred by in situ melting of host rock constituents by shock, as opposed to melt injected into the lherzolitic target. Despite a common origin, NWA 1950 is shocked to a lesser extent compared to Allan Hills (ALH) 77005 (45–55 GPa). Assuming ejection in a single shock event by spallation, this places NWA 1950 near to ALH 77005, but at a shallower depth within the Martian subsurface. Extensive shock melt networks, the interconnectivity between melt pockets, and the ubiquitous presence of highly vesiculated plagioclase glass in ALH 77005 suggests that this meteorite may be transitional between discreet shock melting and bulk rock melting.     

Petrology and mineralogy of the angrite Northwest Africa 1670

Abstract— Northwest Africa (NWA) 1670, contains olivines of up to 5 mm in size representing about 30% of the studied section. With subordinate clinopyroxene and chrome‐spinel microphenocrysts (0.2‐0.5 mm), they represent a xenocrystic association. Phenocrysts are surrounded by a groundmass, predominantly comprising bundles of plagioclase and clinopyroxene (typically 20 × 200 μm crystals). Olivine and kirschsteinite are present in the groundmass in lesser amounts. The olivine xenocrysts (Fo90) are significantly fractured and show mosaicism for their major part, the remaining showing faint undulatory extinction. They are surrounded with a rim of 100–200 μm zoned down to Fo80 and overgrown with serrated olivine, Fo80 to Fo60 (about 100 μm). Olivine in the groundmass is zoned from Mg# 0.55 to 0.15; its CaO content ranges 2.0 to 8.4%. Subcalcic kirschsteinite is zoned from Mg# 0.13 to 0.03, CaO increasing from 15.8 to 21.3%. Pyroxenes xenocrysts (Mg# = 0.77) are superseded in the groundmass by less magnesian pyroxenes, Mg# 0.61 to 0.17, with an average FeO/ MnO of 98. Their compositions range from En₃₀ Fs₂₂ Wo₂₇ Al‐Ts₂₈ Ti‐Ts₂ to En₂ Fs₃₇ Wo₂₂ Al‐Ts₄₀ Ti‐Ts₁. Anorthite microcrysts (An99‐100) are restricted to the groundmass. Accessories are pyrrhotite, kamacite, Ca‐phosphate, titanomagnetite, hercynite and Ca‐carbonate. The bulk chemical composition confirms that NWA 1670 corresponds to a normal angrite melt that incorporated olivine. High Mg olivine xenocrysts and the associated mineralogy are typical of angrites. We suggest that it is an impact melt with relict phenocrysts. The strong silica undersaturation, the presence of Fo90 olivine xenocrysts and carbonate support their derivation as melilite‐like melts in the presence of carbonate.     

Petrogenesis of lunar mare basalt meteorite Miller Range 05035

Abstract— Miller Range (MIL) 05035 is a low‐Ti mare basalt that consists predominantly of pyroxene (62.3 vol%) and plagioclase (26.4 vol%). Pyroxenes are strongly shocked and complexly zoned from augite (Wo₃₃) and pigeonite (Wo₁₇) cores with Mg# = 50–54 to hedenbergite rims. Coexisting pyroxene core compositions reflect crystallization temperatures of 1000 to 1100 °C. Plagioclase has been completely converted to maskelynite with signs of recrystallization. Maskelynite is relatively uniform in composition (An₉₄Ab₆–An₉₁Ab₉), except at contacts with late‐stage mesostasis areas (elevated K contents, An₈₂Ab₁₅Or₃). Symplectites (intergrowth of Fe‐augite, fayalite, and silica) of different textures and bulk compositions in MIL 05035 suggest formation by decomposition of ferro‐pyroxene during shock‐induced heating, which is supported by the total maskelynitization of plagioclase, melt pockets, and the presence of a relict pyroxferroite grain. Petrography and mineral chemistry imply that crystallization of MIL 05035 occurred in the sequence of Fe‐poor pyroxenes (Mg# = 50–54), followed by plagioclase and Fe‐rich pyroxenes (Mg# = 20–50), and finally hedenbergite, Fe‐Ti oxides, and minor late‐stage phases. Petrography, bulk chemistry, mineral compositions, and the age of MIL 05035 suggest it is possibly source crater‐paired with Asuka (A‐) 881757 and Yamato (Y‐) 793169, and may also be launch‐paired with Meteorite Hills (MET) 01210. MIL 05035 represents an old (?3.8–3.9 Ga), incompatible element‐depleted low‐Ti basalt that was not sampled during the Apollo or Luna missions. The light‐REE depleted nature and lack of Eu anomalies for this meteorite are consistent with an origin distant from the Procellarum KREEP Terrane, and genesis from an early cumulate mantle‐source region generated by extensive differentiation of the Moon.     

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.