A transmission electron microscope study of exsolution and coarsening in iron‐bearing clinopyroxene from synthetic analogues of chondrules

Abstract— The microstructure of Fe‐rich clinopyroxene from synthetic analogues of chondrules was studied by transmission electron microscopy. The samples were cooled at various rates from 1455 °C to the quench temperature of 1000 °C. Slow cooling at rates below approximately 50–60 °C/h leads to the development of coherent pigeonite/augite exsolution lamallae on (001). A final wavelength of 19.6 ± 1.1 nm was obtained at a cooling rate of 10 °C/h, and 17.4 ± 2.4 ran at a cooling rate of 50 °C/h. Faster cooling at rates between approximately 50 and 450 °C/h yields only modulated structures with a wavelength on the order of 17–19 nm for the (001) orientation. Coherent exsolution lamellae on (001) in clinopyroxene occur in chondrules of H, L, LL, and CV chondrites, indicating that slow cooling of chondrules at subsolidus temperatures is a widespread phenomenon. The variation of the lamellar wavelength observed in natural chondrules corresponds to a variation of the subsolidus cooling rates between ～0.1 and 50 °C/h. The low cooling rates at subsolidus temperatures deduced from the microstructure of Fe‐rich clinopyroxene point to nonlinear cooling, with cooling rates decreasing with decreasing temperature.     

Pyroxene microstructure in the Northwest Africa 856 martian meteorite

Abstract— Transmission electron microscopy was used to examine pyroxene microstructure in the Northwest Africa (NWA) 856 martian meteorite to construct its cooling and shock histories. All pyroxenes contain strained coherent pigeonite/augite exsolution lamellae on (001). The average width and periodicity of lamellae are 80 and 400 nm, respectively, indicating a cooling rate below 0.1 °C/hr for the parent rock. Pigeonite and augite are topotactic, with strained coherent interfaces parallel to (001). The closure temperature for Ca‐Fe, Mg interdiffusion, estimated from the composition at the augite pigeonite interface, is about 700 °C. Tweed texture in augite reveals that a spinodal decomposition occurred. Locally, tweed evolved toward secondary pigeonite exsolutions on (001). Due to the decreasing diffusion rate with decreasing temperature, “M‐shaped” concentration profiles developed in augite lamellae. Pigeonite contains antiphase boundaries resulting from the C2/c to P2₁/c space group transition that occurred during cooling. The reconstructive phase transition from P2₁/c clinopyroxene to orthopyroxene did not occur. The deformation (shock) history of the meteorites is revealed by the presence of dislocations and mechanical twins. Dislocations are found in glide configuration, with the [001](100) glide system preferentially activated. They exhibit strong interaction with the strained augite/pigeonite interfaces and did not propagate over large distances. Twins are found to be almost all parallel to (100) and show moderate interaction with the augite/pigeonite interfaces. These twins are responsible for the plastic deformation of the pyroxene grains. Comparison with microstructure of shocked clinopyroxene (experimentally or naturally shocked) suggests that NWA 856 pyroxenes are not strongly shocked.     

Cooling rates of type I chondrules from Renazzo: Implications for chondrule formation

Cooling rates are one of the few fundamental constraints on models of chondrule formation. In this study, we used Cu and Ga diffusion profiles in metal grains to determine the cooling rates of type I chondrules in the Renazzo CR2 chondrite. To improve previous estimations of cooling rates obtained using this method, we used CT scanning and serial polishing of our sections to analyze equatorial sections of large metal grains. Through the cores of these metal grains situated at the surface of chondrules, the cooling rates calculated range from 21 to 86 K h⁻¹ for a peak temperature T_p ~ 1623–1673 K. A metal grain embedded in the core of a chondrule exhibits a cooling rate of 1.2 K h⁻¹ at a T_p ~ 1573 K. We also measured Cu-Ga diffusion profiles from nonequatorial sections of metal grains and calculated a lower range of cooling rates of 15–69 K h⁻¹ for T_p ~ 1473–1603 K compared to our results from equatorial sections. The high cooling rates inferred from the lightning model (several thousand K h⁻¹) are clearly at odds with the values obtained in this work. The X-wind model predicts cooling rates (~6–10 K h⁻¹) lower than most of our results. The cooling rates calculated here are in close agreement with those inferred from shock wave models, in particular for temperatures at which olivine crystallizes (from ~10 to several hundreds K h⁻¹ between 1900 and 1500 K). However, the chemical compositions of metal grains in Renazzo are consistent with the splashing model, in which a spray of metal droplets originated from a partially molten planetesimal. Volatile siderophile element depletion is explained by evaporation before metal was engulfed within silicate droplets. Liquid metal isolated from the liquid silicate crystallized during cooling, reacted with the ambient gas, and then re-accreted within partially molten chondrules.     

Silica minerals in cumulate eucrites: Insights into their thermal histories

Some eucrites contain up to 10 vol% silica minerals; however, silica minerals have not been studied in detail so far. We performed a mineralogical study of silica minerals in three cumulate eucrites (Moore County, Moama, and Yamato [Y] 980433). Monoclinic tridymite was common in all three samples. Moama contained orthorhombic tridymite as lamellae within monoclinic tridymite grains. Y 980433 included quartz around an impact melt vein. The presence of orthorhombic tridymite in Moama indicates that Moama cooled more rapidly than the other two samples at low temperatures (<400 °C). This result is different from the slower cooling rates of Moama (?0.0004 °C yr^?1) than that of Moore County (>0.3 °C yr^?1, after the shock event) at high temperatures (>500 °C) estimated from compositional profiles of pyroxene exsolution lamellae. The difference of the cooling rates may reflect their geological settings. Y 980433 cooled slowly at low temperature, as did Moore County. Quartz in Y 980433 could be a local product transformed from monoclinic tridymite by a shock event. We suggest that silica minerals in meteorites record thermal histories at low temperatures and shock events.     

Enstatite chemical composition and microstructures in the La Villa H4 chondrite

Abstract— La Villa is an unshocked H4 chondrite. Chemical compositions require crystallization at temperatures >1250 °C for enstatite and >1211 °C for augite. Widespread (100) polysynthetic twins and (001) contraction cracks in enstatite indicate crystallization as protoenstatite, inverted to either ortho‐ or clinoenstatite or both on cooling. High‐resolution transmission electron microscopy shows a range of ortho‐clinoenstatite intergrowths: heavily faulted clinoenstatite in radial and poikilitic chondrules, almost regular orthoenstatite in a microgranular chondrule and in the matrix. In the former, the clinoenstatite lamellae are both even or odd multiples of the 9Å periodicity, a few unit cells thick, twinned and interleaved with minor orthoenstatite. In the latter, orthoenstatite lamellae are regularly stacked for more than 2000 Å. Localized annealing effects, reversing clinoenstatite to orthoenstatite, are revealed by “U‐shaped” and “Z‐shaped” terminations. The variable microstructures suggest different cooling rates for the different chondrule types, soon after the liquidus‐to‐solidus transition (1200 to 1300 °C) but prior to accretion. In particular, clinoenstatite‐rich crystals from radial and poikilitic chondrules give cooling rates on the order of 100 and 10 °C/h. Comparisons with previous works on dynamic crystallization experiments and orthopyroxene Fe‐Mg cation ordering indicate a nonlinear cooling path from the high chondrule formation temperatures to a postaccretionary low‐temperature (340–480 °C) evolution.     

Crystallization experiments of intercumulus melts for nakhlites under QFM ± 2 at 1 bar

Abstract— Crystallization of parent melts for nakhlites was experimentally studied under QFM ± 2 at one bar. Isothermal experiments suggest that melts having parent magma composition for nakhlites crystallize both augites and titanomagnetites at liquidus temperatures of 1144–1154 °C. Compositions of the augites are identical to those of phenocrystic core augites (En_36–38Fs_22–25Wo_39–40) in nakhlites. No olivines crystallize from the isothermal runs, and solidus temperature is about 1000 °C. Linear‐cooling experiments were carried out at various cooling rates (1–17 °C/h) ranging from liquidus to solidus temperatures under similar pressure conditions to the isothermal runs. Augites, titanomagnetites, and fayalites crystallized in the cooling runs, but magnesian olivines never crystallized there. Magnesian core augite in the cooling runs has the same composition as those of nakhlites. Rims of augite crystals from the cooling runs of 1–4 °C/h consist of two layers, ferroan augite inner rim and hedenbergite outer rim, which are very similar to those in the Miller Range (MIL) 03346 nakhlite. Small amounts of pyroxferroite crystallized in mesostasis and augite rims from two cooling runs. Titanomagnetites from cooling runs never accompany ilmenite lamellae as seen in nakhlites, suggesting that the subsolidus cooling rate of the cooling runs was much more rapid than those of nakhlite intercumulus melts. The cooling experiments reproduce the crystallization processes of pyroxenes and the compositional change of residual melt for a rapidly cooled magma such as MIL 03346.     

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

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

Microtextures and crystal chemistry of pigeonite in the ureilites ALHA77257, RKPA80239, Y‐791538, and ALHA81101

Abstract— The microtextures of pigeonite in four ureilites, Allan Hills (ALH) 77257, Reckling Peak (RKP) A80239, Yamato (Y‐) 791538, and Allan Hills A81101, chosen to span a range of composition and shock level, were investigated by transmission electron microscopy (TEM); two of the samples were also investigated by single crystal X‐ray diffraction to determine Fe²⁺‐Mg cation site partitioning. The low‐shock and compositionally homogeneous pigeonites in ALHA77257 and RKPA80329 (Wo 6.4 for both, mg 86.3 and 84.3 respectively) display irregularly spaced, shock‐induced stacking faults oriented parallel to (100), and large antiphase domains (50–100 nm). Antiphase domains have no preferential orientation. No evidence of exsolution was observed. The low‐shock Y‐791538 pigeonite is homogeneous and has higher Ca and mg (Wo 9.4, mg 91.2). TEM investigation showed spinodal decomposition, indicative of incipient exsolution; small antiphase domains were observed (～5 nm). Single crystal refinement yielded R_4s? = 5.71%, with Fe²⁺‐Mg partitioning coefficient k_d = 0.077(8) and T_c = 658(35) °C. ALHA81101 has compositionally heterogeneous pyroxenes, with large local variations in Wo and mg (Wo = 4–13, mg = 86–68). No compositional gradients from core to rim of grains were observed, and the heterogeneity is interpreted as related to cation migration during shock. In one relatively Ca‐rich region (Wo～12), TEM analysis showed augite‐pigeonite exsolution lamellae, with spacing 145(20) nm. Results for ALHA77257, RKPA80239, and Y‐791538 support a model of rapid cooling following breakup of the ureilite parent body. The presence of exsolution lamellae in ALHA81101 can be related to a local shock‐induced Ca enrichment and provides no constraint on the late cooling history.     

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.     

Thermal history of the Ibitira noncumulate eucrite as inferred from pyroxene exsolution lamella: Evidence for reheating and rapid cooling

Abstract— Ibitira is a strongly recrystallized and unbrecciated noncumulate eucrite. We measured Ca compositional profiles of Ibitira pyroxene by electron microprobe and computed the cooling rate and burial depth from pyroxene exsolution profiles to gain information on early thermal history of Ibitira. Pyroxene begins to exsolve at 1082 °C and cools down to 550 °C at a rate of 0.02 °C/year, forming an augite lamella about 7.0 μm in width. A notable characteristic of the Ca profile of augite lamellae in Ibitira pyroxene is a gradient near the interface between augite and low‐Ca pyroxene (pigeonite). This profile suggests that after thermal metamorphism Ibitira pyroxene experienced a sudden temperature rise to above solidus temperature of pyroxene (～1082 °C), and subsequent rapid cooling. The ³⁹Ar‐⁴⁰Ar age of 4.485 Ga for Ibitira, which is the oldest ³⁹Ar‐⁴⁰Ar age for noncumulate eucrites, may date this reheating event.     

The formation and alteration of the Renazzo‐like carbonaceous chondrites III: Toward understanding the genesis of ferromagnesian chondrules

To better understand the formation conditions of ferromagnesian chondrules from the Renazzo‐like carbonaceous (CR) chondrites, a systematic study of 210 chondrules from 15 CR chondrites was conducted. The texture and composition of silicate and opaque minerals from each observed FeO‐rich (type II) chondrule, and a representative number of FeO‐poor (type I) chondrules, were studied to build a substantial and self‐consistent data set. The average abundances and standard deviations of Cr₂O₃ in FeO‐rich olivine phenocrysts are consistent with previous work that the CR chondrites are among the least thermally altered samples from the early solar system. Type II chondrules from the CR chondrites formed under highly variable conditions (e.g., precursor composition, redox conditions, cooling rate), with each chondrule recording a distinct igneous history. The opaque minerals within type II chondrules are consistent with formation during chondrule melting and cooling, starting as S‐ and Ni‐rich liquids at 988–1350 °C, then cooling to form monosulfide solid solution (mss) that crystallized around olivine/pyroxene phenocrysts. During cooling, Fe,Ni‐metal crystallized from the S‐ and Ni‐rich liquid, and upon further cooling mss decomposed into pentlandite and pyrrhotite, with pentlandite exsolving from mss at 400–600 °C. The composition, texture, and inferred formation temperature of pentlandite within chondrules studied here is inconsistent with formation via aqueous alteration. However, some opaque minerals (Fe,Ni‐metal versus magnetite and panethite) present in type II chondrules are a proxy for the degree of whole‐rock aqueous alteration. The texture and composition of sulfide‐bearing opaque minerals in Graves Nunataks 06100 and Grosvenor Mountains 03116 suggest that they are the most thermally altered CR chondrites.     

Petrology of the Yamato nakhlites

Abstract— The Yamato nakhlites, Y‐000593, Y‐000749, and Y‐000802, were recovered in 2000 from the bare icefield around the Yamato mountains in Antarctica, consisting of three independent specimens with black fusion crusts. They are paired cumulate clinopyroxenites. We obtained the intercumulus melt composition of the Yamato nakhlites and here call it the Yamato intercumulus melt (YIM). The YIM crystallized to form the augite rims, the olivine rims and the mesostasis phases in the cumulates. The augite rims consist of two layers: inner and outer. The crystallization of the inner rim drove the interstitial melt into the plagioclase liquidus field. Subsequently, the residual melt crystallized pigeonites and plagioclase to form the outer rims and the mesostasis. Three types of inclusions were identified in olivine phenocrysts: rounded vitrophyric, angular vitrophyric, and monomineralic augite inclusions. The monomineralic augite inclusions are common and may have been captured by growing olivine phenocrysts. The rounded vitrophyric inclusions are rare and may represent the composition of middle‐stage melts, whereas the angular vitrophyric inclusions seem to have been derived from fractionated late‐stage melts. Glass inclusions occur in close association with titanomagnetite and ferroan augite halo in phenocryst core augites and the assemblages may be magmatic inclusions in augites. We compared the YIM with compositions of magmatic inclusions in olivine and augite. The composition of magmatic inclusions in augite is similar to the YIM. Phenocrystic olivines contain exsolution lamellae, augite‐magnetite aggregates, and symplectites in the cores. The symplectites often occur at the boundaries between olivine and augite grains. The aggregates, symplectite and lamellae formed by exsolution from the host olivine at magmatic temperatures. We present a formational scenario for nakhlites as follows: (1) accumulation of augite, olivine, and titanomagnetite phenocrysts took place on the floor of a magma chamber; (2) olivine exsolved augite and magnetite as augite‐magnetite aggregates, symplectites and lamellae; (3) the overgrowth on olivine phenocrysts formed their rims, and the inner rims crystallized on augite phenocryst cores; and finally, (4) the outer rim formed surrounding the inner rims of augite phenocrysts, and plagioclase and minor minerals crystallized to form mesostasis under a rapid cooling condition, probably in a lava flow or a sill.     

A new calibration to determine the closure temperatures of Fe‐Mg ordering in augite from nakhlites

Recently it has been shown that the relatively low closure temperature (T_c) of 500 (100)°C calculated for augite from Miller Range nakhlite (MIL 03346,13) using the available geothermometers would correspond to a slow cooling rate inconsistent with the petrologic evidence for an origin from a fast‐cooled lava flow. Moreover, previous annealing experiments combined with HR‐SC‐XRD on an augite crystal from MIL 03346 clearly showed that at 600 °C, the Fe²⁺‐Mg degree of order remained unchanged, thus suggesting that the actual T_c is close to this temperature. In order to clarify this discrepancy, we undertook an ex situ annealing experimental study at 700, 800, and 900 °C, until the equilibrium in the intracrystalline Fe²⁺‐Mg exchange is reached, using an augite crystal from Miller Range nakhlite (MIL 03346,13) with a composition of about En₃₆Fs₂₄Wo₄₀. These data allowed us to calculate the following new geothermometer calibration for Martian nakhlites: where The application of this new equation to other Martian nakhlites (NWA 988 and Nakhla) suggests that for augite with composition close to that of MIL 03346, the T_c is up to 170 °C higher with respect to the one calculated using the previous available geothermometer equation, thus suggesting a significantly faster cooling in agreement with petrologic evidence.     

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.     

Symplectic exsolution in olivine from the Nakhla martian meteorite

Abstract— The Nakhla meteorite, commonly accepted to have originated from Mars, is a cumulus clinopyroxenite with ～10 vol% of Fe‐rich olivine. Almost all olivine grains in Nakhla contain dark lamellar inclusions (less than 2–3 μm wide). High‐resolution scanning and transmission electron microscopy revealed that the inclusions are complex intergrowths of augite and magnetite. Such a symplectic intergrowth of augite and magnetite in olivine was known in some terrestrial rocks, lunar rocks, and a few meteorites. The inclusion in Nakhla olivine is the first symplectite found in a martian rock. Apparently, the presence of Fe³+ in olivine under an oxidizing condition on Mars caused symplectic exsolution at high temperature (>900 °C) during cooling.     

Orthopyroxene as a geospeedometer: Thermal history of Kapoeta,Old Homestead 001, and Hughes 002 howardites

Abstract— Single crystals of orthopyroxene from small fragments of the Kapoeta, Old Homestead 001, and Hughes 002 howardites were studied by x‐ray diffraction and microprobe analyses. The Fe‐Mg equilibrium distribution coefficients k_D of the crystals were used to calculate the closure temperatures (T_c) using the calibration by Stimpfl et al. (1999). The compositions, the presence of exsolved augite lamellae, and the T_c values (from 365 to 385 °C) obtained for Kapoeta orthopyroxene s suggest that our fragment comes from a diogenitic cumulate clast. The more Fe‐rich composition, the absence of exsolved lamellae, and the higher T_c values (from 583 to 605 °C) measured in the Old Homestead 001 orthopyroxenes suggest that this fragment comes from a cumulitic clast affected by fast cooling at high temperature. For the Hughes 002 orthopyroxenes, close in composition to Old Homestead 001, the different T_c values (339, 358, and 607 °C) recorded by the various crystals and the presence of augite lamellae in the crystals with the lowest T_c support the hypothesis that this howardite sample is an unheated breccia containing a mixture of cumulitic orthopyroxenes with different thermal histories.     

A layered-crust model of a Howardite parent body

A Howardite parent body is a Vesta-like hypothetical asteroid composed of diogenites, eucrites, and howardites (polymict breccias of various diogenites and eucrites). Combined single-crystal X-ray diffraction and microprobe studies of their pyroxenes indicate that their exsolution and inversion textures vary systematically with respect to their crystallization trend deduced from their Mg and Ca concentrations. Mg-Rich, early crystallized (presumably deep-seated) members revealed slowly cooled textures, except Mg-Rich pyroxene fragments in eucritic polymict breccias. Present study of such pyroxenes in Yamato-74450 and -75015 found in Antarctica confirmed that they were originally cores of the very rapidly cooled Pasamonte-like pigeonites. Based on these data, we reconstructed a layered-crust model from bottom to top as: (A) Mg-rich diogenite layer with orthopyroxenes with or without exsolution lamellae of augite with common (100) plane; (B) Fe-rich diogenite layer with inverted low-Ca pigeonites and orthopyroxenes; (C) cumulate eucrite layer with low-Ca inverted pigeonites with blebby augite inclusions with (100) in common generally, and plagioclase (Binda is the most Mg-rich member of this layer); (D) Moore County-like layer with partially inverted pigeonites with (001) augite lamellae and plagioclase; (E) common eucrite layer with the Juvinas-like pigeonites with fine (001) augite lamellae and plagiocalse; (F) surface eucrite layer with the Pasamonte-like pigeonites which are chemically zoned.     

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

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

Chondrule thermal history from unequilibrated H chondrites: A transmission and analytical electron microscopy study

Abstract— Sixteen texturally different (porphyritic, barred, radial, cryptocrystalline) FeO‐rich chondrules from the unequilibrated ordinary chondrites Brownfield, Frontier Mountain (FRO) 90003 and FRO 90032 were characterized by optical and scanning electron microscopy and then thoroughly studied by transmission and analytical electron microscopy. Nanotextural and nanochemical data indicate similar thermal evolution for chondrules of the same textural groups; minor, yet meaningful differences occur among the different groups. Olivine is the earliest phase formed and crystallizes between 1500 and 1400 °C. Protoenstatite crystallizes at temperatures higher than 1350–1200 °C; it later inverts to clinoenstatite in the 1250–1200 °C range. Enstatite is surrounded by pigeonitic or (less frequently) augitic rims; the minimal crystallization temperature for the rims is 1000 °C; high pigeonite later inverts to low pigeonite, between 935 and 845 °C. The outer pigeonitic or augitic rims are constantly exsolved, producing sigmoidal augite or enstatite precipitates; sigmoidal precipitates record exsolution temperatures between 1000 and 640 °C. Cooling rate (determined using the speedometer based upon ortho‐clinoenstatite intergrowth) was in the order of 50–3000 °C/h at the clinoenstatite‐orthoenstatite transition temperature (close to 1250–1200 °C), but decreased to 5–10 °C/h or slower at the exsolution temperature (between 1000 and 650 °C), thus revealing nonlinear cooling paths. Nanoscale observations indicate that the individual chondrules formed and cooled separately from 1500 °C down to at least 650 °C. Accretion into chondritic parent body occurred at temperatures lower than 650 °C.     

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

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