Basaltic volcanism on the angrite parent body: Comparison with 4 Vesta

Carbon and nitrogen data from stepped combustion analysis of eight angrites, seven eucrites, and two diogenites, alongside literature data from a further nine eucrites and two diogenites, have been used to assess carbon and nitrogen incorporation and isotope fractionation processes on the angrite parent body (APB), for comparison with volatile behavior on the HED parent body (4 Vesta). A subset of the angrite data has been reported previously (Abernethy et al. 2013 ). Two separate families of volatile components were observed. They were (1) moderately volatile material (MVM), mostly combusting between ~500 and 750 °C and indistinguishable from terrestrial contamination and (2) refractory material (RM), mainly released above 750 °C and thought to be carbon (as ) and nitrogen (as N₂ or ) dissolved within the silicate lattice, fitting with the slightly oxidized (~IW to IW+2) angrite fO₂ conditions. Isotopic fractionation trends for carbon and nitrogen within the plutonic and basaltic (quenched) angrites suggest that the behavior of the two volatile elements is loosely coupled, but that the fractionation process differs between the two angrite subgroups. Comparison with results from eucrites and diogenites implies similarities between speciation of carbon and nitrogen on 4 Vesta and the APB, with the latter being more enriched in volatiles than the former.     

Spinel-bearing,Al-rich chondrules in two chondrite finds from Roosevelt County,New Mexico: Indicators of nebular and parent body processes

Abstract— Two rare, spinel-bearing, Al-rich chondrules have been identified in new chondrite finds from Roosevelt County, New Mexico—RC 071 (L4) and RC 072 (L5). These chondrules have unusual mineralogies, dominated by highly and asymmetrically zoned, Al-Cr-rich spinels. Two alternatives exist to explain the origin of this zoning—fractional crystallization or metamorphism. It appears that fractional crystallization formed the zoning of the trivalent cations (Al, Cr) and caused a localized depletion in chromites around the large Al-Cr-rich spinels. The origin of the zoning of the divalent cations (Fe, Mg, Zn) is less certain. Diffusive exchange and partitioning of Fe and Mg between olivine and spinel during parent body metamorphism can explain the asymmetric zoning of these elements. Unfortunately, appropriate studies of natural and experimental systems to evaluate the formation of zoning of the divalent cations by fractional crystallization have not yet been conducted. The bulk compositions of the chondrules suggest affinities with the Na-Al-Cr-rich chondrules, as would be expected from the abundance of Al-Cr-rich spinels. Melting of rare and unusual precursors produced the compositions of Na-Al-Cr-rich chondrules, possibly including a spinel-rich precursor enriched in Cr₂O₃ and ZnO. The two chondrules we studied have larger modal abundances of Al-Cr-rich spinels than reported in other Na-Al-Cr-rich chondrules of similar composition, and Al-rich chondrules even more enriched in spinel are reported in the literature. These differences indicate that factors other than bulk composition control the mineralogy of the chondrules. The most important of these factors are the temperature to which the molten chondrule was heated and the cooling rate during crystallization. These two chondrules cooled rapidly from near the liquidus, as indicated by the zoning, occurrence and sizes of spinels, radiating chondrule textures and localized chromite depletions. The range of mineralogies in other Al-rich chondrules of similar composition reflect a range of peak temperatures and cooling rates. We see no reason to believe that this range is fundamentally different from the range of thermal histories experienced by “normal” Fe-Mg-rich chondrules.     

147Sm‐143Nd and 176Lu‐176Hf systematics of eucrite and angrite meteorites

Comparative planetary geochemistry provides insight into the origin and evolutionary paths of planetary bodies in the inner solar system. The eucrite and angrite achondrite groups are particularly interesting because they show evidence of early planetary differentiation. We present ¹⁴⁷Sm‐¹⁴³Nd and ¹⁷⁶Lu‐¹⁷⁶Hf analyses of eight noncumulate (basaltic) eucrites, two cumulate eucrites, and three angrites, which together place new constraints on the evolution and differentiation histories of the crusts of the eucrite and angrite parent bodies and their mantle mineralogies. The chemical compositions of both eucrites and angrites indicate similar evolutionary paths and petrogenetic models with formation and isolation of differentiated crustal reservoirs associated with segregation of ilmenite. We report a ¹⁴⁷Sm‐¹⁴³Nd mineral isochron age for the Moama cumulate eucrite of 4519 ± 34 Ma (MSWD = 1.3). This age indicates protracted magmatism within deep crustal layers of the eucrite parent body lasting up to about 50 Ma after the formation of the solar system. We further demonstrate that the isotopic compositions of constituent minerals are compromised by secondary processes hindering precise determination of mineral isochron ages of basaltic eucrites and angrites. We interpret the changes in geochemistry and, consequently, the erroneous ¹⁴⁷Sm‐¹⁴³Nd and ¹⁷⁶Lu‐¹⁷⁶Hf internal mineral isochron ages of basaltic eucrites and angrites as the result of metamorphic events such as impacts (effects from pressure, temperature, and peak shock duration) on the surfaces of the eucrite and angrite parent bodies.     

Mineralogy and petrology of the angrite Northwest Africa 1296

Abstract— We report on a new angrite, Northwest Africa (NWA) 1296, a fine‐grained rock with a magmatic texture of rapid cooling. Dendritic olivine (?Fo₅₀) crystallized first in association with anorthite microcrysts (An_98–100) forming composite chains separated from one another by intergrown Al‐Fe diopside‐hedenbergite pyroxenes. In addition, some olivines with lower Mg# and increased CaO (up to 12%) are found between the chains as equant microphenocrysts. Pyroxenes and olivines are both normally zoned from Mg# = 0.52 to less than 0.01 in the rims. Ca‐rich olivines are surrounded by, intergrown with, or replaced by subcalcic kirschsteinite. They appear after plagioclase crystallization stopped, at the end of the crystallization sequence. Minor phases are pyrrhotite, F‐apatite, and titanomagnetite. Pyroxene is the last silicate phase to grow, interstitial to idiomorphic olivine‐kirschsteinite. Numerous small vesicles and some channels are filled with microcristalline carbonate. The mode (vol%) is about 28% olivine, 3% kirschsteinite, 32% anorthite, 34% pyroxene, and 3% of the minor phases—close to that reported previously for D'Orbigny and Sahara (SAH) 99555. The bulk chemical composition of NWA 1296 is similar to D'Orbigny and SAH 99555; NWA 1296 differs by its texture and mineralogy, which are interpreted as resulting from rapid crystallization—an evidence of impact melting. Angrites cannot be produced by partial melting of a CV source because segregation of a “planetary” core is necessary to explain the low FeO/MgO ratio of magnesian olivines. Neither the odd Ca/Al ratio nor the very low SiO₂ content can be explained by conventional partial melting scenarios. We suggest that carbonate is the key to angrite genesis. This is supported by the striking similarities with terrestrial melilitites (low SiO₂, superchondritic Ca/Al ratio, presence of carbonate). The lack of alkalies could be the result of either loss after impact melting or absence of alkalies in the source.     

Effect of chlorine on near‐liquidus crystallization of olivine‐phyric shergottite NWA 6234 at 1 GPa: Implication for volatile‐induced melting of the Martian mantle

Martian magmas are thought to be rich in chlorine compared with their terrestrial counterparts. Here, we experimentally investigate the effect of chlorine on liquidus depression and near‐liquidus crystallization of olivine‐phyric shergottite NWA 6234 and compare these results with previous experimental results on the effect of chlorine on near‐liquidus crystallization of the surface basalts Humphrey and Fastball. Previous experimental results showed that the change in liquidus temperature is dependent on the bulk composition of the basalt. The effect of chlorine on liquidus depression is greater for lower SiO₂ and higher Al₂O₃ magmas than for higher SiO₂ and lower Al₂O₃ magmas. The bulk composition for this study has lower Al₂O₃ and higher FeO contents than previous work; therefore, we provide additional constraints on the effect of the bulk composition on the influence of chlorine on near‐liquidus crystallization. High pressure and temperature crystallization experiments were performed at 1 GPa on a synthetic basalt, of the bulk composition of NWA 6234, with 0–4 wt% Cl added to the sample as AgCl. The results are consistent with previous notions that with increasing wt% Cl in the melt, the crystallization temperature decreases. Importantly, our results have a liquidus depression ?T (°C) from added chlorine that is consistent with the difference in bulk composition and suggest a dependence on both the bulk Al₂O₃ and FeO content. Our results suggest that the addition of chlorine to the Martian mantle may lower magma genesis temperatures and potentially aid in the petrogenesis of Martian magmas.     

Evolution of the angrite parent body: Implications of metamorphic coronas in NWA 3164

Northwest Africa 3164 is a coarse‐grained angrite that shows reaction coronas, a unique character among achondrites. Olivine (Fo₅₇; 1.2 wt% CaO), fassaitic clinopyroxene, anorthite, and spinel account for 46–47, 28–29, 8–13, and 4–8 vol%, respectively; kamacite is an accessory phase. The spinel grains in contact with clinopyroxene are bounded by discontinuous 20 μm thick coronas of anorthite and olivine, indicating the reaction Cpx + Spl → Ol + An (R1). In addition, irregular coronas of clinopyroxene and spinel developed around the primary anorthite in contact with primary olivine, during the reaction Ol + An → Cpx + Spl (R2). R2 also generated clinopyroxene and spinel films between the secondary olivine and anorthite coronas produced during R1, implying that R1 preceded R2. Both are metamorphic reactions that developed in the solid state. Finally, the coronas are cross cut by μm‐thick veinlets due to a late shock. A mass‐balance study shows that R2 is almost the reverse of R1. The P–T metamorphic evolution of the rock, modeled by calculating a P–T isochemical diagram, indicates an equilibrium T of 940 ± 120 °C at P < 0.9 GPa for the initial assemblage, followed by an increase of T up to approximately 1000–1200 °C during reaction R1 and a subsequent cooling during R2. Several causes are envisaged to account for this metamorphic evolution. Contact metamorphism due to a hot magmatic intrusion in the angrite parent body is favored, as similar metamorphic coronas are well known in metamorphic terrestrial rocks. In addition to differentiation and magmatism, there is now evidence for metamorphism in the angrite parent body, which would have been a large asteroid or a planetary‐sized body.     

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.     

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.     

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.     

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

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

Basaltic magmatism and the bulk composition of the moon

The lunar interior is comprised of two major petrological provinces: (1) an outer zone several hundred km thick which experienced partial melting and crystallization differentiation 4.4–4.6 b.y. ago to form the lunar crust together with an underlying complementary zone of ultramafic cumulates and residua, and (2) the primordial deep interior which was the source region for mare basalts (3.2–3.8 b.y.) and had previously been contaminated to varying degrees with highly fractionated material derived from the 4.4–4.6 b.y. differentiation event. In both major petrologic provinces, basaltic magmas have been produced by partial melting. The chemical characteristics and high-pressure phase relationships of these magmas can be used to constrain the bulk compositions of their respective source regions.Primitive low-Ti mare basalts (e.g., 12009, 12002, 15555 and Green Glass) possessing high normative olivine and high Mg and Cr contents, provide the most direct evidence upon the composition of the primordial deep lunar interior. This composition, as estimated on the basis of high pressure equilibria displayed by the above basalts, combined with other geochemical criteria, is found to consist of orthopyroxene + clinopyroxene + olivine with total pyroxenes > olivine, 100 MgO/(MgO + FeO) = 75–80, about 4% of CaO and Al₂O₃ and 2× chondritic abundances of REE, U and Th. This composition is similar to that of the earth's mantle except for a higher pyroxene/olivine ratio and lower 100 MgO/(MgO + FeO).The lunar crust is believed to have formed by plagioclase elutriation within a vast ocean of parental basaltic magma. The composition of the latter is found experimentally by removing liquidus plagioclase from the observed mean upper crust (gabbroic anorthosite) composition, until the resulting composition becomes multiply saturated with plagioclase and a ferromagnesian phase (olivine). This parental basaltic composition is almost identical with terrestrial oceanic tholeiites, except for partial depletion in the two most volatile components, Na₂ and SiO₂. Similarity between these two most abundant classes of lunar and terrestrial basaltic magmas strongly implies corresponding similarities between their source regions. The bulk composition of the outer 400 km of the Moon as constrained by the 4.6-4.4 b.y. parental basaltic magma is found to be peridotitic, with olivine > pyroxene, 100 MgO/ (MgO + FeO) 86, and about 2× chondritic abundances of Ca, Al and REE. The Moon thus appears to have a zoned structure, with the deep interior (below 400 km) possessing somewhat higher contents of FeO and SiO₂ than the outer 400 km. This zoned model, derived exclusively on petrological grounds, provides a quantitative explanation of the Moon's mean density, moment of inertia and seismic velocity profile.The bulk composition of the entire Moon, thus obtained, is very similar to the pyrolite model composition for the Earth's mantle, except that the Moon is depleted in Na (and other volatile elements) and somewhat enriched in iron. The similarity in major element composition extends also to the abundances of REE, U and Th. These compositional similarities, combined with the identity in oxygen isotope ratios between the Moon and the Earth's mantle, are strongly suggestive of a common genetic relationship.     

Petrology,mineralogy, and oxygen isotope compositions of aluminum‐rich chondrules from CV3 chondrites

Bulk major element composition, petrography, mineralogy, and oxygen isotope compositions of twenty Al‐rich chondrules (ARCs) from five CV3 chondrites (Northwest Africa [NWA] 989, NWA 2086, NWA 2140, NWA 2697, NWA 3118) and the Ningqiang carbonaceous chondrite were studied and compared with those of ferromagnesian chondrules and refractory inclusions. Most ARCs are marginally Al‐richer than ferromagnesian chondrules with bulk Al₂O₃ of 10–15 wt%. ARCs are texturally similar to ferromagnesian chondrules, composed primarily of olivine, pyroxene, plagioclase, spinel, Al‐rich glass, and metallic phases. Minerals in ARCs have intermediate compositions. Low‐Ca pyroxene (Fs_0.6–8.8Wo_0.7–9.3) has much higher Al₂O₃ and TiO₂ contents (up to 12.5 and 2.3 wt%, respectively) than that in ferromagnesian chondrules. High‐Ca pyroxene (Fs_0.3–2.0Wo_33–54) contains less Al₂O₃ and TiO₂ than that in Ca,Al‐rich inclusions (CAIs). Plagioclase (An_77–99Ab_1–23) is much more sodic than that in CAIs. Spinel is enriched in moderately volatile element Cr (up to 6.7 wt%) compared to that in CAIs. Al‐rich enstatite coexists with anorthite and spinel in a glass‐free chondrule, implying that the formation of Al‐enstatite was not due to kinetic reasons but is likely due to the high Al₂O₃/CaO ratio (7.4) of the bulk chondrule. Three ARCs contain relict CAIs. Oxygen isotope compositions of ARCs are also intermediate between those of ferromagnesian chondrules and CAIs. They vary from ?39.4‰ to 13.9‰ in δ¹⁸O and yield a best fit line (slope = 0.88) close to the carbonaceous chondrite anhydrous mineral (CCAM) line. Chondrules with 5–10 wt% bulk Al₂O₃ have a slightly more narrow range in δ¹⁸O (?32.5 to 5.9‰) along the CCAM line. Except for the ARCs with relict phases, however, most ARCs have oxygen isotope compositions (>?20‰ in δ¹⁸O) similar to those of typical ferromagnesian chondrules. ARCs are genetically related to both ferromagnesian chondrules and CAIs, but the relationship between ARCs and ferromagnesian chondrules is closer. Most ARCs were formed during flash heating and rapid cooling processes like normal chondrules, only from chemically evolved precursors. ARCs extremely enriched in Al and those with relict phases could have had a hybrid origin (Krot et al. 2002) which incorporated refractory inclusions as part of the precursors in addition to ferromagnesian materials. The occurrence of melilite in ARCs indicates that melilite‐rich CAIs might be present in the precursor materials of ARCs. The absence of melilite in most ARCs is possibly due to high‐temperature interactions between a chondrule melt and the solar nebula.     

The water content and parental magma of the second chassignite NWA 2737: Clues from trapped melt inclusions in olivine

NWA 2737, the second known chassignite, mainly consists of cumulate olivine crystals of homogeneous composition (Fo = 78.7 ± 0.9). These brown colored olivine grains exhibit two sets of perpendicular planar defects due to shock. Two forms of trapped liquids, interstitial melts and magmatic inclusions, have been examined. Mineral assemblages within the olivine‐hosted magmatic inclusions include low‐Ca pyroxene, augite, kaersutite, fluorapatite, biotite, chromite, sulfide, and feldspathic glass. The reconstructed parental magma composition (A^#) of the NWA 2737 is basaltic and resembles both the experimentally constrained parental melt composition of chassiginites and the Gusev basalt Humphrey, albeit with lower Al contents. A^# also broadly resembles the average of shergottite parent magmas or LAR 06319. However, we suggest that the mantle source for the chassignite parental magmas was distinct from that of the shergottite meteorites, particularly in CaO/Al₂O₃ ratio. In addition, based on the analysis of the volatile contents of kaersutite, we derived a water content of 0.48–0.67 wt% for the parental melt. Finally, our MELTS calculations suggest that moderate pressure (approximately 6.8 kb) came closest to reproducing the crystallized melt‐inclusion assemblages.     

Petrogenetic models for magmatism on the eucrite parent body: Evidence from orthopyroxene in diogenites

Abstract— Diogenites are recognized as a major constituent of the howardite, eucrite and diogenite (HED) meteorite group. Recently, several papers (Mittlefehldt, 1994; Fowler et al, 1994, 1995) have identified trace-element systematics in diogenites that appeared to mimic simple magmatic processes that involved large degrees of crystallization (up to 95% orthopyroxene) of basalt with extremely high normative hypersthene. Such a crystallization scenario linking all the diogenites is highly unlikely. The purpose of this study is to explore other possible models relating the diogenites. Computational major-element melting models of a variety of different potential bulk compositions for the eucrite parent body (EPB) mantle indicate that these compositions show a similar sequence in residuum mineral assemblage with increasing degrees of partial melting. Numerous bulk compositions would produce melts with Mg# appropriate for diogenitic parent magmas at low to moderate degrees of partial melting (15% to 30%). These calculations also show that melts with similar Mg# and variable incompatible element concentrations may be produced during small to moderate degrees of EPB mantle melting. The trace-element characteristic of the orthopyroxene in diogenites does not support a model for large amounts of fractional crystallization of a single “hypersthene normative” basaltic magma following either small-scale or large-scale EPB mantle melting. Small degrees of fractional crystallization of a series of distinct basaltic magmas are much more likely. Only two melting models that we considered hold any promise for producing different batches of “diogenitic magmas.” The first model involves the fractional melting of a homogeneous source that produces parental magmas to diogenites with an extensive range of incompatible elements and limited variations in Mg#. There are several requirements for this model to work. The first requirement of this model is that the D^{orthopyroxene/melt} must change during melting or crystallization to compress the range of incompatible elements in the calculated diogenitic magmas. The second prerequisite is that either some of the calculated diogenitic magmas are parental to eucrites or the Mg# in diogenitic magmas are influenced by slight changes in oxygen fugacity during partial melting. The second model involves batch melting of a source that reflects accretional heterogeneities capable of generating diogenitic magmas with the calculated Mg# and incompatible element contents. Both of these models require small to moderate degrees of partial melting that may limit the efficiency of core separation.     

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

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

Transmission electron microscope study of compact Type A calcium-aluminum-rich inclusions from CV3 chondrites: Clues to their origin

Abstract— A transmission electron microscope (TEM) study of three coarse-grained Type A Ca, Al-rich inclusions (CAIs) from Allende, Acfer 082 and Acfer 086 (all CV3 chondrites) was performed in order to decipher their origin and effects of possible metamorphism. The constituent minerals of the CAIs are found to exhibit very similar microstructural characteristics in each of the inclusions studied. In general, the minerals show a well-developed equilibrium texture with typical 120° triple junctions. Melilites are clearly considerably strained and characterized by high dislocation densities up to 3 × 10¹¹ cm^?2. The dislocations have Burgers vectors of [001], [110] or [011] and often form subgrain boundaries subparallel {100}. Melilite in the Allende CAI additionally contains thin amorphous lamellae mostly oriented parallel to {001}. Fassaite (Al-Ti-diopside) is almost featureless even on the TEM scale. Only a few subplanar dislocation walls composed of dislocations with Burgers vectors [001] and 1/2 [110] were detected. Although enclosed within the highly strained melilites, the euhedral spinels contain only low dislocation densities (<2 × 10⁴ cm^?2). In the Allende CAI, spinels were found twinned on {111}. Perovskite is also characterized by a low number of linear lattice defects. All grains possess orthorhombic symmetry and are commonly twinned according to a 90° rotation around [101]. Many crystals exhibit typical domain structures as well as curved twin walls where two orthogonal sets intersect. In addition to the mineral phases described above, tiny inclusions of the simple oxides CaO and TiO₂ were found within melilite (CaO), spinel (CaO, TiO₂) and perovskite (CaO, TiO₂). Based on these observations, it is assumed that at the beginning of the formation of the CAIs a condensed solid precursor was present. Euhedral spinels poikilitically enclosed within melilites suggest that this solid aggregate was then molten. If the pure oxides represent relict condensates, their presence proves that this melting was incomplete. While still plastic, the CAIs were shocked by microimpacts causing the high dislocation densities in melilite as well as diaplectic melilite glass and twinned spinels in the Allende CAI. In Acfer 082 and 086, the deformation took place at elevated temperatures, preventing the solid phase transition and mechanical twinning. The absence of linear lattice defects in spinel, fassaite and perovskite most probably reflects inhomogeneous pressure distribution in the polycrystalline CAI as well as the different strengths of the minerals. According to cooling-rate experiments on perovskite by Keller and Buseck (1994), the dominating (101) twins in the CAI perovskites point to cooling rates ≤50 °C/min. Finally, after crystallization of the CAI was complete, mild thermal metamorphism caused the formation of subgrain boundaries, 120° triple junctions and chemical homogenization of the melilites.     

Magnetite in the unequilibrated CK chondrites: Implications for metamorphism and new insights into the relationship between the CV and CK chondrites

Bulk isotopic and elemental compositions of CV and CK chondrites have led to the suggestion that both originate from the same asteroid. It has been argued that magnetite compositions also support this model; however, magnetite has been studied almost exclusively in the equilibrated (type 4‐6) CKs. Magnetite in seven unequilibrated CKs analyzed here is enriched in MgO, TiO₂, and Al₂O₃ relative to the equilibrated CKs, suggesting that magnetite compositions are affected by metamorphism. Magnetite in CKs is compositionally distinct from CVs, particularly in abundances of Cr₂O₃, NiO, and TiO₂. Although there are minor similarities between CV and equilibrated CK chondrite magnetite, this is contrary to what we would expect if the CVs and CKs represent a single metamorphic sequence. CV magnetite should resemble CK3 magnetite, as both were metamorphosed to type 3 conditions. Oxygen fugacities and temperatures of CV_ox and CK chondrites are also difficult to reconcile using existing CV‐CK parent body models. Mineral chemistries, which eliminate issues of bulk sample heterogeneity, provide a reliable alternative to techniques that involve a small amount of sample material. CV and CK chondrite magnetite has distinct compositional differences that cannot be explained by metamorphism.     

Origin of a metamorphosed lithic clast in CM chondrite Grove Mountains 021536

Abstract– A metamorphosed lithic clast was discovered in the CM chondrite Grove Mountains 021536, which was collected in the Antarctica by the Chinese Antarctic Research Exploration team. The lithic clast is composed mainly of Fe‐rich olivine (Fo₆₂) with minor diopside (Fs_9.7–11.1Wo_48.3–51.6), plagioclase (An_43–46.5), nepheline, merrillite, Al‐rich chromite (21.8 wt% Al₂O₃; 4.43 wt% TiO₂), and pentlandite. Δ¹⁷O values of olivine in the lithic clast vary from ?3.9‰ to ?0.8‰. Mineral compositions and oxygen isotopic compositions of olivine suggest that the lithic clast has an exotic source different from the CM chondrite parent body. The clast could be derived from strong thermal metamorphism of pre‐existing chondrule that has experienced low‐temperature anhydrous alteration. The lithic clast is similar in mineral assemblage and chemistry to a few clasts observed in oxidized CV3 chondrites (Mokoia and Yamato‐86009) and might have been derived from the interior of the primitive CV asteroid. The apparent lack of hydration in the lithic clast indicates that the clast accreted into the CM chondrite after hydration of the CM components.     

Neodymium,strontium and chromium isotopic studies of the LEW86010 and Angra dos Reis meteorites and the chronology of the angrite parent body

Abstract— Neodymium, strontium, and chromium isotopic studies of the LEW86010 angrite established its absolute age and the formation interval between its crystallization and condensation of Allende CAIs from the solar nebula. Pyroxene and phosphate were found to contain ～98% of its Sm and Nd inventory. A conventional ¹⁴⁷Sm-¹⁴³Nd isochron yielded an age of 4.53 ± 0.04 Ga (2 σ) and ?¹⁴³ _Nd = 0.45 ± 1.1. An ¹⁴⁶Sm-¹⁴²Nd isochron gives initial ¹⁴⁶Sm/¹⁴⁴Sm = 0.0076 ± 0.0009 and ?¹⁴³ _Nd = ?2.5 ± 0.4. The Rb-Sr analyses give initial ⁸⁷Sr/⁸⁶Sr (I⁸⁷_Sr) = 0.698972 ± 8 and 0.698970 ± 18 for LEW and ADOR, respectively, relative to ⁸⁷Sr/⁸⁶Sr = 0.71025 for NBS987. The difference, ΔI⁸⁷_Sr, between I⁸⁷_Sr for the angrites and literature values for Allende CAIs, corresponds to ～9 Ma of growth in a solar nebula with a CI chondrite value of ⁸⁷Rb/⁸⁶Sr = 0.91, or ～5 Ma in a nebula with solar photospheric ⁸⁷Rb/⁸⁶Sr = 1.51. Excess ⁵³Cr from extinct ⁵³Mn (t1/2 = 3.7 Ma) in LEW86010 corresponds to initial ⁵³Mn/⁵⁵Mn = 1.44 ± 0.07 × 10^?6 and closure to Cr isotopic homogenization 18.2 ± 1.7 Ma after formation of Allende inclusions, assuming initial ⁵³Mn/⁵⁵Mn = 4.4 ± 1.0 × 10^?5 for the inclusions as previously reported by the Paris group (Birck and Allegre, 1988). The ¹⁴⁶Sm/¹⁴⁴Sm value found for LEW86010 corresponds to solar system initial (¹⁴⁶Sm/¹⁴⁴Sm)_o = 0.0080 ± 0.0009 for crystallization 8 Ma after Allende, the difference between Pb-Pb ages of angrites and Allende, or 0.0086 ± 0.0009 for crystallization 18 Ma after Allende, using the Mn-Cr formation interval. The isotopic data are discussed in the context of a model in which an undifferentiated “chondritic” parent body formed from the solar nebula ～2 Ma after Allende CAIs and subsequently underwent differentiation accompanied by loss of volatiles. Parent bodies with Rb/Sr similar to that of CI, CM, or CO chondrites could satisfy the Cr and Sr isotopic systematics. If the angrite parent body had Rb/Sr similar to that of CV meteorites, it would have to form slightly later, ～2.6 Ma after the CAIs, to satisfy the Sr and Cr isotopic systematics.     

Magnesium oxide-iron oxide mass balance constraints and a more detailed model for the relationship between eucrites and diogenites

Abstract— According to a currently popular model for petrogenesis on the howardite, eucrite, and diogenite (HED) parent asteroid, the diogenites are not comagmatic with most eucrites but instead formed in separate orthopyroxenite-dominated plutons. This model can be tested for consistency with mass balance for MgO and FeO, assuming the overall diogenite/(diogenite + eucrite) ratio, d, of the parent asteroid is at least comparable to the average d for the eucrite + diogenite dominated howardite regolith breccias. Average mg# (=MgO/[MgO + FeO]) is much lower for eucrites, especially noncumulate eucrites, than for diogenites. Unless the diogenite parent magmas eventually produced a large proportion of low-mg# residual basalt and gabbro (RBG), the implied initial magma's mg# is vastly higher than that of any noncumulate eucrite. Starting from a source previously depleted by putative primary eucrite genesis, melt mg# can be estimated as a function of the exchange reaction K_D and degree of melting. Using several very conservative assumptions (e.g., assuming that the total [MgO + FeO] concentration is nearly the same in the nascent melt as in the residual solids), the degree of melting required to yield a melt with mg# high enough to satisfy mass balance, without implying an RBG component that accounts for >50% of all eucrites, is an implausibly high 60–80 wt%. The separate orthopyroxenitic plutons (SOP) model also seems inconsistent with the uniform density of melts across the diogenite-eucrite compositional spectrum (2.77–2.82 g/cm³), which implies that diogenitic magmas should have been as capable as eucrites of extruding to form lavas. This difficulty cannot be reduced by simply assuming that later-formed magmas were systematically both more plutonic and more MgO-rich than earlier ones, because the plutonic cumulate eucrites equilibrated with melts systematically lower in mg# than noncumulate eucrites. Conceivably, the bulk mg# of the asteroid's silicate system was increased between primary-melt eucrite genesis and SOP diogenite genesis by graphite-fueled reduction of FeO. However, the graphite oxidation process generates a huge proportion of gas, which would have enhanced the buoyancy of the nascent diogenite-parent magmas, thus exacerbating the difficulty of achieving the implied high degrees of partial melting. To avoid these difficulties but still form most eucrites as rapidly cooled extrusives, I propose the NERD (noncumulate eucrites as extruded residua of diogenites) model. In this model, the diogenites form as early cumulates from a large magma system (probably a global “magma ocean”) that yields a large proportion of eucritic melt as residuum. This residual melt zone undergoes relatively little crystallization during a period when it is episodically tapped to produce extrusions, dikes and sills of rapidly cooled noncumulate eucrites. Slight (～5–10%) porosity in the nascent eucritic crust keeps it marginally buoyant over the residual melt zone. The common thermal metamorphism of noncumulate eucrites results from baking by superjacent flows during the episodic venting of the melt zone. The NERD model's greatest advantage is that it does not require implausibly high degrees of localized melting in the mature stages of igneous evolution of the HED asteroid.