Parent body depth–pressure–temperature relationships and the style of the ureilite anatexis

Abstract– New analyses of mafic silicates from 14 ureilite meteorites further constrain a strong correlation ( Singletary and Grove 2003 ) between olivine‐core Fo ratio and the temperature of equilibration (T_E) recorded by the composition of pigeonite. This correlation may be compared with relationships implied by various postulated combinations of Fo and pressure P in models for ureilite genesis by a putative process of anatectic (depth‐linked, P‐controlled) smelting. In such models, any combination of Fo and P together fixes the temperature of smelting. Agreement between the observed correlation and these models is poor. The anatectic smelting model also carries implausible implications for the depth range at which ureilites of a given composition (Fo) form. Actual ureilites (and polymict ureilite clasts: Downes et al. 2008 ) show a distribution strongly skewed toward the low‐Fo end of the compositional range, with approximately 58% in the range Fo_76–81. In contrast, the P‐controlled smelting model implies that the Fo_76–81 region is a small fraction of the volume of the parent body: not more than 3.2%, in a model consistent with the Fo‐T_E observations; and even ignoring the Fo‐T_E evidence not more than 11% (percentages cited require optimal assumptions concerning the size of the parent body). This region also must occur deep within the body, where no straightforward model would imply a strong bias in the impact‐driven sampling process. The ureilites did not derive preponderantly from one atypical “largest offspring” disruption survivor, because cooling history evidence shows that after the disruption (whose efficiency was increased by gas jetting), all of the known ureilites cooled in bodies that were tiny (mass of order 10^?9) in comparison with the precursor body. The Ca/Al ratio of the ureilite starting matter cannot be 2.5 times chondritic, as has been suggested, unless the part of the body from which ureilites come is at most 50% of the whole body. Published variants of the anatectic, P‐controlled smelting model have the ureilites coming from a region that is >50 vol% of their parent body; and to invoke a larger body would have the drawback of implying that the Fo_76–81 spike represents an even smaller fraction of the parent body’s interior. The ureilites’ moderate depletions in incompatible elements are difficult to reconcile with a fractional fusion model. It is not plausible that melt formed grossly out of equilibrium with the medium‐sized ureilite crystals. The alternative to pressure‐controlled smelting, i.e., a model of gasless or near‐gasless anatexis, has very different implications for the size and evolution of the original parent body. To yield internal pressures prohibitive of smelting in even the shallowest and most ferroan portion of its anatectic mantle, the body would have to be larger than roughly 690 km in diameter. A 400 km body would have approximately 12 vol% of the interior (or 13 vol% of the interior apart from the thermal “skin” that never undergoes anatexis) prone, if both extremely shallow and extremely ferroan, to mild smelting. Gasless anatexis also implies that this large parent body was compositionally, at least in terms of mg, grossly heterogeneous before anatexis, probably (in view of the oxygen isotopic diversity) as a result of mixed accretion.     

Early petrologic processes on the ureilite parent body

Abstract— We present a petrographic and petrologic analysis of 21 olivine‐pigeonite ureilites, along with new experimental results on melt compositions predicted to be in equilibrium with ureilite compositions. We conclude that these ureilites are the residues of a partial melting/smelting event. Textural evidence preserved in olivine and pigeonite record the extent of primary smelting. In pigeonite cores, we observe fine trains of iron metal inclusions that formed by the reduction of olivine to pigeonite and metal during primary smelting. Olivine cores lack metal inclusions but the outer grain boundaries are variably reduced by a late‐stage reduction event. The modal proportion of pigeonite and percentage of olivine affected by late stage reduction are inversely related and provide an estimation of the degree of primary smelting during ureilite petrogenesis. In our sample suite, this correlation holds for 16 of the 21 samples examined. Olivine‐pigeonite‐liquid phase equilibrium constraints are used to obtain temperature estimates for the ureilite samples examined. Inferred smelting temperatures range from ～1150°C to just over 1300°C and span the range of estimates published for ureilites containing two or more pyroxenes. Temperature is also positively correlated with modal percent pigeonite. Smelting temperature is inversely correlated with smelting depth—the hottest olivine‐pigeonite ureilites coming from the shallowest depth in the ureilite parent body. The highest temperature samples also have oxygen isotopic signatures that fall toward the refractory inclusion‐rich end of the carbonaceous chondrite‐anhydrous mineral (CCAM) slope 1 mixing line. These temperature‐depth variations in the ureilite parent body could have been created by a heterogeneous distribution of heat producing elements, which would indicate that isotopic heterogeneities existed in the material from which the ureilite parent body was assembled.     

Ureilite petrogenesis: A limited role for smelting during anatexis and catastrophic disruption

Abstract— A popular model for ureilites assumes that during anatexis in an asteroidal mantle, pressure‐buffered equilibrium smelting (partial reduction coincident with partial melting) engendered their conspicuous mafic‐silicate‐core mg diversity (75–96 mol%). Several mass‐balance problems arise from this hypothesis. Smelting inevitably consumes a large proportion of any plausible initial carbon while generating significant proportions of Fe metal and copious proportions of CO gas. The most serious problem concerns the yield of CO gas. If equilibrium smelting produced the ureilites’ entire 21 mol% range in olivine‐core mg, the proportion of gas within the asteroidal mantle (assuming plausibly low pressure <～80 bar) should have reached ≥85 vol%. Based on the remarkably stepwise cooling history inferred from ureilite texture and mineralogy, a runaway, CO‐leaky process that can loosely be termed smelting appears to have occurred, probably triggered by a major impact. The runaway scenario appears likely because, by Le Chǎtelier's principle, CO leakage would tend to accelerate the smelting process. Also, the copious volumes of gas produced by smelting would have led to explosive, mass‐leaky eruptions into the vacuum surrounding the asteroid. Loss of mass would mean diminution of interior pressure, which would induce further smelting, leading to further loss of mass (basalt), and so on. Such a disruptive runaway process may have engendered the ureilites’ distinctive reduced olivine rims. But the only smelting, according to this scenario, was a short‐lived disequilibrium process that reduced only the olivine rims, not the cores; and the ureilites were cooling, not melting, during the abortive “smelting” episode.     

Origin of mass‐independent oxygen isotope variation among ureilites: Clues from chondrites and primitive achondrites

Ureilite meteorites are abundant, carbon‐rich, primitive achondrites made of coarse‐grained, equilibrated olivine and pyroxene (usually pigeonite). They probably sample the baked, heterogeneous, melt‐depleted mantle of a large, once‐chondritic parent body that was broken up catastrophically while still young and hot. Heterogeneity in the parent body is inferred from a considerable “slope‐1” variation from one meteorite to another in oxygen isotopes (?2.5‰ < Δ¹⁷O < ?0.2‰), which correlates with both molar FeO/MgO (range 0.03–0.35) and molar FeO/MnO (range 3–57), i.e., Δ¹⁷O correlates with the redox state. No consensus has yet emerged on the cause of these correlated trends. One view favors their inheritance via silicates from hot nebular (preaccretion) processes. Another invokes smelting (reduction of FeO by C in the hot parent body). Here, guided mainly by similar trends among equilibrated ordinary and R chondrites, studies of their unequilibrated counterparts, and work on other primitive achondrites, we propose a new model for ureilites in which the parent body accreted nebular ice with high‐?¹⁷O, Mg‐rich silicates with low ?¹⁷O, and varying amounts of metallic iron. Water from the thawing ice then oxidized the metal yielding secondary FeO‐bearing minerals with high ?¹⁷O that, with metamorphism, became incorporated into the ureilite silicates. FeO/MgO, FeO/MnO, and ?¹⁷O correlate because they rose in unison by amounts that varied spatially, depending on the local amount of metal that was oxidized. We suggest that the parent body was so large (radius ? 100 km) that smelting was inhibited and that carbon played a passive role in ureilite evolution. Although ureilites are regarded as complicated meteorites, we believe our analysis explains their mass‐independent oxygen isotope trend and related FeO variation through well‐understood processes and enlightens our understanding of the evolution of early planetesimals from cold, wet bodies to hot, dry ones.     

Si‐bearing metal and niningerite in Almahata Sitta fine‐grained ureilites and insights into the diversity of metal on the ureilite parent body

A detailed mineralogical and chemical study of Almahata Sitta fine‐grained ureilites (MS‐20, MS‐165, MS‐168) was performed to shed light on the origin of these lithologies and their sulfide and metal. The Almahata Sitta fine‐grained ureilites (silicates <30 μm grain size) show textural and chemical evidence for severe impact smelting as described for other fine‐grained ureilites. Highly reduced areas in Almahata Sitta fine‐grained ureilites show large (up to ～1 mm) Si‐bearing metal grains (up to ～4.5 wt% Si) and niningerite [Mg_>0.5,(Mn,Fe)_<0.5S] with some similarities to the mineralogy of enstatite (E) chondrites. Overall, metal grains show a large compositional variability in Ni and Si concentrations. Niningerite grains probably formed as a by‐product of smelting via sulfidation. The large Si‐Ni variation in fine‐grained ureilite metal could be the result of variable degrees of reduction during impact smelting, inherited from coarse‐grained ureilite precursors, or a combination of both. Large Si‐bearing metal grains probably formed via coalescence of existing and newly formed metal during impact smelting. Bulk and in situ siderophile trace element abundances indicate three distinct populations of (1) metal crystallized from partial melts in MS‐20, (2) metal resembling bulk chondritic compositions in MS‐165, and (3) residual metal in MS‐168. Almahata Sitta fine‐grained ureilites developed their distinctive mineralogy due to severe reduction during smelting. Despite the presence of E chondrite and ureilite stones in the Almahata Sitta fall, a mixing relation of E chondrites or their constituents and ureilite material in Almahata Sitta can be ruled out based on isotopic, textural, and mineral‐chemical reasons.     

Ureilite petrogenesis: A limited role for smelting during anatexis and catastrophic disruption

Abstract— A popular model for ureilites assumes that during anatexis in an asteroidal mantle, pressure‐buffered equilibrium smelting (partial reduction coincident with partial melting) engendered their conspicuous mafic‐silicate‐core mg diversity (75–96 mol%). Several mass‐balance problems arise from this hypothesis. Smelting inevitably consumes a large proportion of any plausible initial carbon while generating significant proportions of Fe metal and copious proportions of CO gas. The most serious problem concerns the yield of CO gas. If equilibrium smelting produced the ureilites' entire 21 mol% range in olivine‐core mg, the proportion of gas within the asteroidal mantle (assuming plausibly low pressure <˜80 bar) should have reached ≥85 vol%. Based on the remarkably stepwise cooling history inferred from ureilite texture and mineralogy, a runaway, CO‐leaky process that can loosely be termed smelting appears to have occurred, probably triggered by a major impact. The runaway scenario appears likely because, by Le Châtelier's principle, CO leakage would tend to accelerate the smelting process. Also, the copious volumes of gas produced by smelting would have led to explosive, mass‐leaky eruptions into the vacuum surrounding the asteroid. Loss of mass would mean diminution of interior pressure, which would induce further smelting, leading to further loss of mass (basalt), and so on. Such a disruptive runaway process may have engendered the ureilites' distinctive reduced olivine rims. But the only smelting, according to this scenario, was a short‐lived disequilibrium process that reduced only the olivine rims, not the cores; and the ureilites were cooling, not melting, during the abortive “smelting” episode.     

Northwest Africa 1500: Plagioclase‐bearing monomict ureilite or ungrouped achondrite?

Abstract— Northwest Africa (NWA) 1500 is an ultramafic meteorite dominated by coarse (?100–500 μm) olivine (95–96%), augite (2–3%), and chromite (0.6–1.6%) in an equilibrated texture. Plagioclase (0.7–1.8%) occurs as poikilitic grains (up to ?3 mm) in vein‐like areas that have concentrations of augite and minor orthopyroxene. Other phases are Cl‐apatite, metal, sulfide, and graphite. Olivine ranges from Fo 65–73, with a strong peak at Fo 68–69. Most grains are reversezoned, and also have ?10–30 μm reduction rims. In terms of its dominant mineralogy and texture, NWA 1500 resembles the majority of monomict ureilites. However, it is more ferroan than known ureilites (Fo ≥75) and other mineral compositional parameters are out of the ureilite range as well. Furthermore, neither apatite nor plagioclase have ever been observed, and chromite is rare in monomict ureilites. Nevertheless, this meteorite may be petrologically related to the rare augite‐bearing ureilites and represent a previously unsampled part of the ureilite parent body (UPB). The Mn/Mg ratio of its olivine and textural features of its pyroxenes are consistent with this interpretation. However, its petrogenesis differs from that of known augite‐bearing ureilites in that: 1) it formed under more oxidized conditions; 2) plagioclase appeared before orthopyroxene in its crystallization sequence; and 3) it equilibrated to significantly lower temperatures (800–1000 °C, from two‐pyroxene and olivine‐chromite thermometry). Formation under more oxidized conditions and the appearance of plagioclase before orthopyroxene could be explained if it formed at a greater depth on the UPB than previously sampled. However, its significantly different thermal history (compared to ureilites) may more plausibly be explained if it formed on a different parent body. This conclusion is consistent with its oxygen isotopic composition, which suggests that it is an ungrouped achondrite. Nevertheless, the parent body of NWA 1500 may have been compositionally and petrologically similar to the UPB, and may have had a similar differentiation history.     

Alkali‐feldspathic material entrained in Fe,S‐rich veins in a monomict ureilite

Abstract— The Elephant Moraine (EET) 96001 ureilite contains a remarkable diversity of feldspars, which occur as tiny (no more than 60 μm maximum dimension) grains within a few Fe,S‐rich (now weathered to mostly Fe oxide) veins. Molar S: Fe ratio in the veins averages 0.08 ± 0.02. The veins meander and feature large fluctuations in apparent width; they appear to have entered this monomict breccia by a gentle, percolative process, not by violent impact injection. The feldspars are accompanied by a diverse suite of K‐rich (and generally also Ti‐rich) feldspathic glasses, and also major proportions of silica and pyroxene, which is largely fassaitic. A rhönite‐like phase is also found, and, as inclusions in one of the fassaites, a Cr‐poor spinel‐like phase. The feldspars mostly feature remarkably high K/Na compared to feldspars of comparable An from polymict ureilites. The EET 96001 feldspathic component was probably once part of a thin basaltic crust on a ureilite asteroid. The spinel included in one of the fassaites formed at remarkably high f0₂ (apparent oxidation state of iron: ～41 atom% Fe³⁺), suggesting that the parent magma possibly assimilated near‐surface water (however, the Fe³⁺ was not directly measured, and has conceivably been affected by terrestrial weathering; also, there is no assurance that this fassaite originated together with the typical feldspar). We speculate that the feldspathic component was mixed into the dense, Fe,S‐rich vein material, and very soon thereafter the Fe,S‐rich vein material was emplaced adjacent to the EET 96001 host ureilite, at an advanced stage in a chaotic catastrophic disruption and partial reassembly process that affected all ureilites. The high‐K nature of the EET 96001 feldspathic component, including the feldspathic glasses, suggests that fractional fusion may not have been as common during ureilite anatexis as has been inferred from recent studies of clast assemblages in polymict ureilites.     

Ureilites: A critical review

Abstract— Ureilites are coarse-grained ultramafic rocks whose petrography, mineral chemistry, lithophile element bulk chemistry, and Sm-Nd isotopic systematics suggest that they are highly fractionated igneous rocks and thus are products of common planetary differentiation processes. However, they also have primitive characteristics that are difficult to reconcile with extensive igneous processing. These include high abundances of siderophile elements, planetary-type noble gases, and the oxygen isotopic signature of unequilibrated solar system materials. The incongruity between igneous and primitive features constitutes the most important problem in understanding ureilite petrogenesis. In this review the petrographic, chemical, and isotopic characteristics of ureilites are summarized, and the petrogenetic implications of these characteristics are discussed. The most important constraints on ureilite petrogenesis are: 1) Ureilites have lost a basaltic complement; 2) Ureilites had a two-stage cooling history; 3) Ureilites are probably residues but partly crystallized from melts; 4) Ureilites are derived from a minimum of six reservoirs which were distinct in oxygen isotopic composition and did not equilibrate with one another; 5) A correlation between oxygen isotopic composition and mg ratio was established in ureilite parent material in the solar nebula; 6) If carbon-metal-silicate-CO/CO₂ equilibrium was maintained then the mg ratios of ureilites were pressure/depth-dependent; however, if the pressure was sufficiently high (> 100–200 bars) that a CO/CO₂ gas phase was not present then carbon and metal could have been at equilibrium with all ureilite mg ratios at the same pressure; 7) Ureilites either lost a low-melting temperature metal fraction or gained a refractory-rich metal component; 8) Primordial noble gases were retained in carbon in ureilites; 9) The ultramafic ureilite assemblage formed at ～4.55 Ga, but Sm-Nd and Rb-Sr isotopic systematics have been subsequently disturbed. Recently proposed models for ureilite petrogenesis are evaluated in terms of how well they satisfy these constraints; no models unequivocally satisfy all of them. Reconciling constraints 5 and 6 requires a large ureilite parent body.     

Microdistributions and petrogenetic implications of rare earth elements in polymict ureilites

Abstract— Polymict ureilites contain various mineral and lithic clasts not observed in monomict ureilites, including plagioclase, enstatite, feldspathic melt clasts and dark inclusions. This paper investigates the microdistributions and petrogenetic implications of rare earth elements (REEs) in three polymict ureilites (Elephant Moraine (EET) 83309, EET 87720 and North Haig), focusing particularly on the mineral and lithic clasts not found in monomict ureilites. As in monomict ureilites, olivine and pyroxene are the major heavy (H)REE carriers in polymict ureilites. They have light (L)REE‐depleted patterns with little variation in REE abundances, despite large differences in major element compositions. The textural and REE characteristics of feldspathic melt clasts in the three polymict ureilites indicate that they are most likely shocked melt that sampled the basaltic components associated with ureilites on their parent body. Simple REE modeling shows that the most common melt clasts in polymict ureilites can be produced by 20–30% partial melting of chondritic material, leaving behind a ureilitic residue. The plagioclase clasts, as well as some of the high‐Ca pyroxene grains, probably represent plagioclase‐pyroxene rock types on the ureilite parent body. However, the variety of REE patterns in both plagioclase and melt clasts cannot be the result of a single igneous differentiation event. Multiple processes, probably including shock melting and different sources, are required to account for all the REE characteristics observed in lithic and mineral clasts. The C‐rich matrix in polymict ureilites is LREE‐enriched, like that in monomict ureilites. The occurrence of Ce anomalies in C‐rich matrix, dark inclusions and the presence of the hydration product, iddingsite, imply significant terrestrial weathering. A search for ²⁶Mg excesses, from the radioactive decay of ²⁶Al, in the polymict ureilite EET 83309 was negative.     

The magnetic effects of brecciation and shock in meteorites: II. The ureilites and evidence for strong nebular magnetic fields

We have examined the magnetic characteristics of representative ureilites, with a view to identify the magnetic effects of shock and to isolate a primary component of the natural remanent magnetization (NRM). As a group, the ureilites show remarkably uniform patterns of magnetic behavior, attesting to a common genesis and history. However, a clearly observed gradation in magnetic properties of the ureilites studied with shock level, parallels their classification based on petrologic and chemical fractionation shock-related trends.The ureilite meteorites possess a strong and directionally stable NRM. Laboratory thermal modelling of this presumably primordial NRM preserved in Goalpara and Kenna produced reliable paleointensity estimates of order 1 Oe, thus providing evidence for strong early, nebular magnetic fields. This paleofield strength is compatible with values obtained previously from carbonaceous chondrites and supports isotopic evidence for a contemporary origin of these two groups of meteorites in the same nebular region. The mechanism for recording nebular fields, manifestly different in carbonaceous chondrite vs. ureilite meteorites, is thus relatively unimportant: violent collisional shock in ureilites seems to have only partially altered an original magnetization, by preferential removal of its least stable portion.     

Magmatic inclusions and felsic clasts in the Dar al Gani 319 polymict ureilite

Abstract— Magmatic inclusions occur in type II ureilite clasts (olivine‐orthopyroxene‐augite assemblages with essentially no carbon) and in a large isolated plagioclase clast in the Dar al Gani (DaG) 319 polymict ureilite. Type I ureilite clasts (olivine‐pigeonite assemblages with carbon), as well as other lithic and mineral clasts in this meteorite, are described in Ikeda et al.(2000). The magmatic inclusions in the type II ureilite clasts consist mainly of magnesian augite and glass. They metastably crystallized euhedral pyroxenes, resulting in feldspar component‐enriched glass. On the other hand, the magmatic inclusions in the large plagioclase clast consist mainly of pyroxene and plagioclase, with a mesostasis. They crystallized with a composition along the cotectic line between the pyroxene and plagioclase liquidus fields. DaG 319 also contains felsic lithic clasts that represent various types of igneous lithologies. These are the rare components not found in the common monomict ureilites. Porphyritic felsic clasts, the main type, contain phenocrysts of plagioclase and pyroxene, and their groundmass consists mainly of plagioclase, pyroxene, and minor phosphate, ilmenite, chromite, and/or glass. Crystallization of these porphyritic clasts took place along the cotectic line between the pyroxene and plagioclase fields. Pilotaxitic felsic clasts crystallized plagioclase laths and minor interstitial pyroxene under metastable conditions, and the mesostasis is extremely enriched in plagioclase component in spite of the ubiquitous crystallization of plagioclase laths in the clasts. We suggest that there are two crystallization trends, pyroxene‐metal and pyroxene‐plagioclase trends, for the magmatic inclusions and felsic lithic clasts in DaG 319. The pyroxene‐metal crystallization trend corresponds to the magmatic inclusions in the type II ureilite clasts and the pilotaxitic felsic clasts, where crystallization took place under reducing and metastable conditions, suppressing precipitation of plagioclase. The pyroxene‐plagioclase crystallization trend corresponds to the magmatic inclusions in the isolated plagioclase clast and the porphyritic felsic clasts. This trend developed under oxidizing conditions in magma chambers within the ureilite parent body. The felsic clasts may have formed mainly from albite component‐rich silicate melts produced by fractional partial melting of chondritic precursors. The common monomict ureilites, type I ureilites, may have formed by the fractional partial melting of alkali‐bearing chondritic precursors. However, type II ureilites may have formed as cumulates from a basaltic melt.     

The Miller Range 090340 and 090206 meteorites: Identification of new brachinite‐like achondrites with implications for the diversity and petrogenesis of the brachinite clan

Miller Range (MIL) 090340 and MIL 090206 are olivine‐rich achondrites originally classified as ureilites. We investigate their petrography, mineral compositions, olivine Cr valences, equilibration temperatures, and (for MIL 090340) oxygen isotope compositions, and compare them with ureilites and other olivine‐rich achondrites. We conclude that they are brachinite‐like achondrites that provide new insights into the petrogenesis of brachinite clan meteorites. MIL 090340,6 has a granoblastic texture and consists of ~97 modal % by area olivine (Fo = molar Mg/[Mg+Fe] = 71.3 ± 0.6). It also contains minor to trace augite, chromite, chlorapatite, orthopyroxene, metal, troilite, and terrestrial Fe‐oxides. Approximately 80% by area of MIL 090206,5 has a granoblastic texture of olivine (Fo 72.3 ± 0.1) plus minor augite and chromite, similar to MIL 090340 but also containing minor plagioclase. The rest of the section consists of a single crystal of orthopyroxene (~11 × 3 mm), poikilitically enclosing rounded grains of olivine (Fo = 76.1 ± 0.6), augite, chromite, metal, and sulfide. Equilibration temperatures for MIL 090340 and MIL 090206, calculated from olivine‐spinel, olivine‐augite, and two‐pyroxene thermometry range from ~800 to 930 °C. In both samples, symplectic intergrowths of Ca‐poor orthopyroxene + opaque phases (Fe‐oxides, sulfide, metal) occur as rims on and veins/patches within olivine. Before terrestrial weathering, the opaques were probably mostly sulfide, with minor metal. All petrologic properties of MIL 090340 and MIL 090206 are consistent with those of brachinite clan meteorites, and largely distinct from those of ureilites. Oxygen isotope compositions of olivine in MIL 090340 (δ¹⁸O = 5.08 ± 0.30‰, δ¹⁷O = 2.44 ± 0.21‰, and Δ¹⁷O = ?0.20 ± 0.12‰) are also within the range of brachinite clan meteorites, and well distinguished from ureilites. Olivine Cr valences in MIL 090340 and the granoblastic area of MIL 090206 are 2.57 ± 0.06 and 2.59 ± 0.07, respectively, similar to those of three brachinites also analyzed here (Brachina, Hughes 026, Nova 003). They are higher than those of olivine in ureilites, even those containing chromite. The valence systematics of MIL 090340, MIL 090206, and the three analyzed brachinites (lower Fo = more oxidized Cr) are consistent with previous evidence that brachinite‐like parent bodies were inherently more oxidized than the ureilite parent body. The symplectic orthopyroxene + sulfide/metal assemblages in MIL 090340, MIL 090206, and many brachinite clan meteorites have superficial similarities to characteristic “reduction rims” in ureilites. However, they differ significantly in detail. They likely formed by reaction of olivine with S‐rich fluids, with only minor reduction. MIL 090340 and the granoblastic area of MIL 090206 are similar in modal mineralogy and texture to most brachinites, but have higher Fo values typical of brachinite‐like achondrites. The poikilitic pyroxene area of MIL 090206 is more typical of brachinite‐like achondrites. The majority of their properties suggest that MIL 090340 and MIL 090206 are residues of low‐degree partial melting. The poikilitic area of MIL 090206 could be a result of limited melt migration, with trapping and recrystallization of a small volume of melt in the residual matrix. These two samples are so similar in mineral compositions, Cr valence, and cosmic ray exposure ages that they could be derived from the same lithologic unit on a common parent body.     

Shock,post‐shock annealing,and post‐annealing shock in ureilites

Abstract— The thermal and shock histories of ureilites can be divided into four periods: 1) formation, 2) initial shock, 3) post‐shock annealing, and 4) post‐annealing shock. Period 1 occurred ?4.55 Ga ago when ureilites formed by melting chondritic material. Impact events during period 2 caused silicate darkening, undulose to mosaic extinction in olivines, and the formation of diamond, lonsdaleite, and chaoite from indigenous carbonaceous material. Alkali‐rich fine‐grained silicates may have been introduced by impact injection into ureilites during this period. About 57% of the ureilites were unchanged after period 2. During period 3 events, impact‐induced annealing caused previously mosaicized olivine grains to become aggregates of small unstrained crystals. Some ureilites experienced reduction as FeO at the edges of olivine grains reacted with C from the matrix. Annealing may also be responsible for coarsening of graphite in a few ureilites, forming euhedral‐appearing, idioblastic crystals. Orthopyroxene in Meteorite Hills (MET) 78008 may have formed from pigeonite by annealing during this period. The Rb‐Sr internal isochron age of ?4.0 Ga for MET 78008 probably dates the annealing event. At this late date, impacts are the only viable heat source. About 36% of ureilites experienced period 3 events, but remained unchanged afterwards. During period 4, ?7% of the ureilites were shocked again, as is evident in the polymict breccia, Elephant Moraine (EET) 83309. This rock contains annealed mosaicized olivine aggregates composed of small individual olivine crystals that exhibit undulose extinction. Ureilites may have formed by impact‐melting chondritic material on a primitive body with heterogeneous O isotopes. Plagioclase was preferentially lost from the system due to its low impedance to shock compression. Brief melting and rapid burial minimized the escape of planetary‐type noble gases from the ureilitic melts. Incomplete separation of metal from silicates during impact melting left ureilites with relatively high concentrations of trace siderophile elements.     

Ureilite smelting

Abstract— Ureilites containing homogeneous Fo₇₆ olivine cores in intimate co-existence with graphite must have recrystallized at pressures of at least ～100 bars to suppress smelting of the fayalite component of the olivine to Fe metal. Smelting of olivine and pyroxene-saturated magmatic liquids produces orthopyroxene-without-olivine crystalline derivatives unlike those in ureilites. Thus the Mg# compositional variation within the ureilite suite, which is commonly attributed to partial smelting, cannot plausibly be produced by assemblages rich in liquid. In situ smelting of graphitic olivine + pigeonite crystal mushes can produce the correct crystal assemblage, but fails to provide a plausible account for the removal of metal from ureilites or for the correlation of Mg# with Δ¹⁷O. Even if Mg# and Δ¹⁷O variations are established in the nebula, ureilite recrystallization with graphite must have occurred at pressures greater than the minima we have experimentally established, corresponding to parent objects not less than ～100 km in radius.     

Differentiation processes in FeO‐rich asteroids revealed by the achondrite Lewis Cliff 88763

Olivine‐dominated (70–80 modal %) achondrite meteorite Lewis Cliff (LEW) 88763 originated from metamorphism and limited partial melting of a FeO‐rich parent body. The meteorite experienced some alteration on Earth, evident from subchondritic Re/Os, and redistribution of rhenium within the sample. LEW 88763 is texturally similar to winonaites, has a Δ¹⁷O value of ?1.19 ± 0.10‰, and low bulk‐rock Mg/(Mg+Fe) (0.39), similar to the FeO‐rich cumulate achondrite Northwest Africa (NWA) 6693. The similar bulk‐rock major‐, minor‐, and trace‐element abundances of LEW 88763, relative to some carbonaceous chondrites, including ratios of Pd/Os, Pt/Os, Ir/Os, and ¹⁸⁷Os/¹⁸⁸Os (0.1262), implies a FeO‐ and volatile‐rich precursor composition. Lack of fractionation of the rare earth elements, but a factor of approximately two lower highly siderophile element abundances in LEW 88763, compared with chondrites, implies limited loss of Fe‐Ni‐S melts during metamorphism and anatexis. These results support the generation of high Fe/Mg, sulfide, and/or metal‐rich partial melts from FeO‐rich parent bodies during partial melting. In detail, however, LEW 88763 cannot be a parent composition to any other meteorite sample, due to highly limited silicate melt loss (0 to <<5%). As such, LEW 88763 represents the least‐modified FeO‐rich achondrite source composition recognized to date and is distinct from all other meteorites. LEW 88763 should be reclassified as an anomalous achondrite that experienced limited Fe,Ni‐FeS melt loss. Lewis Cliff 88763, combined with a growing collection of FeO‐rich meteorites, such as brachinites, brachinite‐like achondrites, the Graves Nunataks (GRA) 06128/9 meteorites, NWA 6693, and Tafassasset, has important implications for understanding the initiation of planetary differentiation. Specifically, regardless of precursor compositions, partial melting and differentiation processes appear to be similar on asteroidal bodies spanning a range of initial oxidation states and volatile contents.     

ROOSEVELT COUNTY 027: A LOW-SHOCK UREILITE WITH INTERSTITIAL SILICATES AND HIGH NOBLE GAS CONCENTRATIONS

The lightly-shocked ureilite RC027 was found in Roosevelt County, New Mexico in 1984. In terms of petrography, texture, mineral compositions, bulk chemical composition, and oxygen isotopic composition it is a typical ureilite. It contains ～75% olivine (Fo 79.4) and 25% pigeonite (mg 81.3, Wo 8.0), with intergranular graphite and (Fe, Ni) metal. It also contains less than 1% of fine-grained, interstitial silicate material, which had not previously been recognized in any ureilite. This material is an assemblage of low-Ca pyroxene (Wo 3.5–9, mg 87–93), augite (Wo 24–36, mg 90–98), glass (typically ～95% SiO₂, 4% Al₂O₃, 0.5% Na₂O), and crystalline SiO₂. This material has an igneous texture, indicating that it crystallized from an interstitial liquid. Low-Ca pyroxene compositions indicate that the interstitial liquid was not in equilibrium with core pigeonite and olivine and cannot have been either an evolved intercumulus liquid or a low-degree partial melt. It may contain a component of shock-melted olivine and pigeonite, although petrographic evidence indicates that it could not have been an in situ shock melt. One sample of RC027 has a V-shaped rare earth element pattern, typical of ureilites. Another is depleted in light rare earth elements (LREE), similar to acid-treated samples of ureilites, which suggests that LREE in ureilites are contained in an inhomogeneously-distributed phase. RC027 shows the strongest olivine preferred-orientation yet observed in a ureilite. Its fabric is characteristic of fabrics formed by tabular minerals in a fluid laminar flow regime and is unlike those formed by syntectonic recrystallization and plastic flow. The elemental and isotopic compositions of noble gases in RC027 are typical of previously analyzed ureilites. This result indicates that there is no correlation of noble gas content with degree of shock in ureilites, and thus suggests that the gases were present in the ureilite material before shock. Cosmogenic He and Ne contents indicate cosmic ray exposure ages of 1.7 and 1.9 Myr, respectively. Thus, RC027 is not paired with Kenna (a ureilite also found in Roosevelt County), which has an exposure age of ～33 Myr.     

Mineralogy and cooling history of the calcium-aluminum-chromium enriched ureilite,Lewis Cliff 88774

Abstract— The LEW 88774 ureilite is extraordinarily rich in Ca, Al, and Cr, and mineralogically quite different from other ureilites in that it consists mainly of exsolved pyroxene, olivine, Cr-rich spinel, and C. The presence of coarse exsolved pyroxene in LEW 88774 is unique because pyroxene in most other ureilites is not exsolved. The pyroxene has bulk Wo contents of 15–20 mol% and has coarse exsolution lamellae of augite and low-Ca pyroxene, 50 μm in width. The compositions of the exsolved augite (Ca_33.7Mg_52.8Fe_13.5) and host low-Ca pyroxene (Ca_4.4Mg₇₅Fe_20.6) show that these exsolution lamellae were equilibrated at 1280 °C. A computer simulation of the cooling rate, obtained by solving the diffusion equation for reproducing the diffusion profile of CaO across the lamellae, suggests that the pyroxene was cooled at 0.01 °C/year until the temperature reached 1160 °C. This cooling rate corresponds to a depth of at least 1 km in the parent body, assuming it was covered by a rock-like material. Therefore, LEW 88774 was held at this high temperature for 1.2 × 10⁴years. The proposed cooling history is consistent with that of other ureilites with coarsegrained unexsolved pigeonites. Lewis Cliff 88774 includes abundant Cr-rich spinel in comparison with other ureilites. The range of FeO content of spinels in LEW 88774 is from 1.3 wt% to 21 wt% [Fe/(Fe + Mg) = 0.04–0.6]. The Cr-rich and Fe-poor spinel in LEW 88774 has less Fe (FeO, 1.3 wt%) than spinels in other achondrites. We classify this spinel as an Fe, Al-bearing picrochromite. Most ureilites are depleted in Ca and Al, but this meteorite has high-Ca and Al concentrations. In this respect, as well as mineral assemblage and the presence of coarse exsolution lamellae in pyroxene, LEW 88774 is a unique ureilite. Most differentiated meteorites are poor in volatile elements such as Zn, but the LEW 88774 spinels contain abundant Zn (up to 0.6 wt%). We note that such a high Zn concentration in spinel has been observed in the carbonaceous chondrites and recrystallized chondrites. This unusual ureilite has more primitive characteristics than most other ureilites.     

TEM investigations on the monomict ureilites Jalanash and Hammadah al Hamra 064

Abstract— We studied the petrography and mineralogy of two monomict ureilites, Hammadah al Hamra 064 (HH064) and Jalanash, by using reflected light and scanning electron microscopy. Quantitative analyses were performed by electron microprobe and the microstructures were investigated with transmission electron microscopy (TEM). HH064 features two different textures, a poikilitic and a typical one, whereas Jalanash shows only the typical ureilite texture. Our synergetic chemical and microstructural investigations reveal a complex cooling history for both ureilites. The temperature for the first equilibrium deduced from the pigeonite‐augite assemblage in HH064 is ～1200°C. The presence of antiphase domains in low‐Ca pyroxenes proves that they are clearly pigeonite. The occurrences of tweed micro structure and orthopyroxene lamellae, which are incompletely developed, imply a faster cooling rate from the first equilibrium with a sudden end. Although both ureilites contain shock induced diamonds, dislocations in silicates are rare. This observation suggests that the meteorites were hot at the time of strong shock metamorphism or that they were heated after strong shock metamorphism. After this event, new microstructural features were generated by different cooling processes and were frozen by a final rapid decrease in temperature possibly due to excavation from the ureilite parent body, or bodies.     

Are ureilites residues from partial melting of chondritic material? The answer from MAGPOX

Abstract— Calculations performed using MAGPOX show that no bulk compositions having chondritic Ca/Al ratio and within the range of chondritic Si/Mg ratios can produce the olivine-pigeonite ureilites (which constitute 65% of those for which modal abundances are known) as residues of single-stage equilibrium partial melting. Calcium/aluminum ratios of 2–3.5 × CI are required. In addition, all the ureilites could not have formed from a single composition at various degrees of reduction, because they show no correlation between pigeonite/olivine ratio and mg ratio. Materials with various Al/Mg ratios, ranging from subchondritic to superchondritic, are required. If these materials are primitive (i.e., created by nebular processes rather than planetary igneous processes), they are unknown in the meteorite record. Excess accretion (relative to chondrites) of 5–10 mol% of a high-temperature condensate component, which was itself almost completely depleted in corundum due to early fractionation, could create the necessary compositions. The plausibility that such processes occurred on a parent-body sized scale is difficult to assess. In contrast, lodranites can be produced as residues of ～3–30% equilibrium partial melting of an average ordinary chondritic composition at the appropriate level of reduction. Although many features of ureilites suggest that they are relatively primitive residues produced by low degrees of melting of chondritic materials, and thus resemble lodranites and other groups of primitive achondrites, their predominantly pigeonite + olivine mineralogy remains difficult to explain within this simple scenario.