Origin of kamacite,schreibersite, and perryite in metal‐sulfide nodules of the enstatite chondrite Sahara 97072 (EH3)

Abstract– Perryite [(Fe,Ni)_x(Si,P)_y], schreibersite [(Fe,Ni)₃P], and kamacite (αFeNi) are constituent minerals of the metal‐sulfide nodules in the Sahara 97072 (EH3) enstatite chondrite meteorite. We have measured concentrations of Ni, Cu, Ga, Au, Ir, Ru, and Pd in these minerals with laser ablation, inductively coupled plasma mass spectrometry (ICP‐MS). We also measured their Fe, Ni, P, Si, and Co concentrations with electron microprobe. In kamacite, ratios of Ru/Ir, Pd/Ir, and Pd/Ru cluster around their respective CI values and all elements analyzed plot near the intersection of the equilibrium condensation trajectory versus Ni and the respective CI ratios. In schreibersite, the Pd/Ru ratio is near the CI value and perryite contains significant Cu, Ga, and Pd. We propose that schreibersite and perryite formed separately near the condensation temperatures of P and Si in a reduced gas and were incorporated into Fe‐Ni alloy. Upon further cooling, sulfidation of Fe in kamacite resulted in the formation of additional perryite at the sulfide interface. Still later, transient heating re‐melted this perryite near the Fe‐FeS eutectic temperature during partial melting of the metal‐sulfide nodules. The metal‐sulfide nodules are pre‐accretionary objects that retain CI ratios of most siderophile elements, although they have experienced transient heating events.     

FeO‐rich silicates in the Sahara 97159 (EH3) enstatite chondrite: Mineralogy,oxygen isotopic compositions,and origin

Abstract— We report the mineralogy and oxygen isotopic compositions of FeO‐rich silicates in the Sahara 97159 EH3 chondrite. This component is referred to as FeO‐rich because it contains substantially more FeO than the characteristic FeO‐poor silicates in the highly reduced enstatite meteorites. These FeO‐rich silicates are mostly low‐Ca pyroxene (Fs5–35) and their compositions suggest an origin under more oxidizing conditions, like those for the ordinary chondrites. However, the mafic silicates in ordinary and carbonaceous chondrites are dominantly olivine, and the FeO‐rich silicates in the E chondrites are less commonly olivine. The oxygen isotopic compositions of the FeO‐rich silicates are indistinguishable from those of FeO‐poor silicates in Sahara 97159. These observations suggest that both the FeO‐rich silicates and the FeO‐poor silicates in EH chondrites formed from the same oxygen reservoir where redox conditions varied widely.     

The formation conditions of enstatite chondrites: Insights from trace element geochemistry of olivine‐bearing chondrules in Sahara 97096 (EH3)

We report in situ LA‐ICP‐MS trace element analyses of silicate phases in olivine‐bearing chondrules in the Sahara 97096 (EH3) enstatite chondrite. Most olivine and enstatite present rare earth element (REE) patterns comparable to their counterparts in type I chondrules in ordinary chondrites. They thus likely share a similar igneous origin, likely under similar redox conditions. The mesostasis however frequently shows negative Eu and/or Yb (and more rarely Sm) anomalies, evidently out of equilibrium with olivine and enstatite. We suggest that this reflects crystallization of oldhamite during a sulfidation event, already inferred by others, during which the mesostasis was molten, where the complementary positive Eu and Yb anomalies exhibited by oldhamite would have possibly arisen due to a divalent state of these elements. Much of this igneous oldhamite would have been expelled from the chondrules, presumably by inertial acceleration or surface tension effects, and would have contributed to the high abundance of opaque nodules found outside them in EH chondrites. In two chondrules, olivine and enstatite exhibit negatively sloped REE patterns, which may be an extreme manifestation of a general phenomenon (possibly linked to near‐liquidus partitioning) underlying the overabundance of light REE observed in most chondrule silicates relative to equilibrium predictions. The silicate phases in one of these two chondrules show complementary Eu, Yb, and Sm anomalies providing direct evidence for the postulated occurrence of the divalent state for these elements at some stage in the formation reservoir of enstatite chondrites. Our work supports the idea that the peculiarities of enstatite chondrites may not require a condensation sequence at high C/O ratios as has long been believed.     

Petrographic and mineralogical study of new EH melt rocks and a new enstatite chondrite grouplet

Abstract— Enstatite chondrites are classified into EH and EL groups, and some of them were melted once. In this paper, we report petrography and mineral chemistry of five new Antarctic enstatite chondrites. Yamato 793225 is characterized by intermediate properties between the EH and EL groups and probably represents a new grouplet of enstatite chondrites. The three paired meteorites (Y-8404, Y-8414 and Y-86004) may have cooled rapidly near the surface of the parent body as impact EH melt rocks. Yamato 82189 is also classified as EH melt rock, but it experienced slow cooling as did Y-793225. Yamato 82189 contains the first occurrence of phlogopite in enstatite meteorites.     

Properties of chondrules in EL3 chondrites,comparison with EH3 chondrites,and the implications for the formation of enstatite chondrites

Abstract— The study of chondrules provides information about processes occurring in the early solar system. In order to ascertain to what extent these processes played a role in determining the properties of the enstatite chondrites, the physical and chemical properties of chondrules from three EL3 chondrites and three EH3 chondrites have been examined by optical, cathodoluminescence (CL), and electron microprobe techniques. Properties examined include size, texture, CL, and composition of both individual phases and bulk chondrules. The textures, distribution of textures, and composition of silicates of the EL3 chondrules resemble those of EH3 chondrules. However, the chondrules from the two classes differ in that (1) the size distribution of the EL chondrules is skewed to larger values than EH chondrules, (2) the enstatite in EL chondrules displays varying shades of red CL due to the presence of fine‐grained sulfides and metal in the silicates, and (3) the mesostasis of EH chondrules is enriched in Na relative to that of EL chondrules. The similarities between the chondrules of the two classes suggest similar precursor materials, while the differences suggest that there was not a single reservoir of meteoritic chondrules, but that their origin was fairly local. The differences in the size distribution of chondrules in EH and EL chondrites may be explained by aerodynamic and gravitational sorting during accumulation of the meteoric material, while differences in CL and mesostasis properties may reflect differences in formation conditions and cooling rate following chondrule formation. We argue that our observations are consistent with the formation of enstatite chondrites in a thick dynamic regolith on their parent body.     

Molecular study of insoluble organic matter in Kainsaz CO3 carbonaceous chondrite: Comparison with CI and CM IOM

Abstract— Kainsaz CO3 insoluble organic matter (IOM) was studied using Curie point pyrolysis, electronic paramagnetic resonance (EPR), and high‐resolution transmission electron microscopy (HRTEM) to determine the effect of thermal metamorphism on molecular chondritic fingerprints. Pyrolysis released a very low amount of products that consist of one‐ and two‐ring aromatic units with methyl, dimethyl, and ethyl substituents. Moreover, Kainsaz IOM contains two orders of magnitude fewer radicals than Orgueil, Murchison, and Tagish Lake IOM. In addition, no diradicaloids were found in Kainsaz, although they are thought to constitute a specific signature for weakly organized extraterrestrial organic compounds in contrast to terrestrial ones. HRTEM reveals a very heterogeneous structure, with microporous disordered carbon, mesoporous graphitic carbons and graphite. Graphitization likely occurs and explains the differences between Kainsaz and CI or CM IOM. Heating stress experienced by Kainsaz IOM, on the parent body and/or prior its accretion, is likely responsible for the differences in molecular and structural organizations compared with those of CI and CM IOM.     

Evidence for a late thermal event of unequilibrated enstatite chondrites: A Rb-Sr study of Qingzhen and Yamato 6901 (EH3) and Khairpur (EL6)

Abstract— The Rb-Sr whole rock and internal systematics of two EH3 chondrites, Qingzhen and Yamato 6901, and of one EL6 chondrite, Khairpur, were determined. Sulfides were separated using a stepwise dissolution technique. The mineral species in each fraction were estimated based on the chemical analyses of 12 major elements. The internal Rb-Sr systematics of the EH3 chondrites are highly disturbed. Fractions corresponding to sulfide phases show excess ⁸⁷Sr, while other fractions corresponding to silicate phases produce a linear trend on a Rb-Sr evolution diagram. If these linear relations are interpreted as isochrons, the ages of the silicate phases are 2.12 ± 0.23 Ga and 2.05 ± 0.33 Ga with the initial Sr isotopic ratios of 0.7112 ± 0.0018 and 0.7089 ± 0.0032, for Qingzhen and Yamato 6901, respectively. The process of the isotopic disturbance probably involved the breakdown of the major K-bearing sulfide (djerfisherite), and a lack of isotopic exchange between sulfide and silicate phases indicates moderate temperatures of reheating. Although a complete Sr isotopic re-homogenization among silicate phases was not attained, we interpret the Rb-Sr results as indicative of a late thermal event about 2 Ga ago on the parent bodies of these EH3 chondrites. These ages agree well with previously published K-Ar ages. An older isochron age of 4.481 ± 0.036 Ga with a low initial Sr isotopic ratio of 0.69866 ± 0.00038 was obtained for the data from silicate fractions of Khairpur, indicating early petrological equilibration on the parent body of EL6 chondrites.     

The Kaidun meteorite: Composition and origin of inclusions in the metal of an enstatite chondrite clast

Abstract— Metal nodules are one of the major textural components of Kaidun sample #01.3.06 EH3-4. In terms of structure, the nodules are of three types: (1) globular, (2) zoned with a massive core and globular mantle, and (3) nodules with no internal structure. The size and composition of the globules in the nodules and grains of metal of the matrix are almost identical: no greater than 20 μm and Ni, 5.95; Si, 3.33 wt%. The nodules contain small (usually <5 μm) inclusions of SiO₂; albitic glass; enstatite; roedderite; and a mixture of SiO₂ and Na₂S₂. This is the first reported occurrence of a simple sulfide of an alkaline metal in nature. The formation of the inclusions appears to be related to condensation of material onto the surfaces of metal grains. The nodules appear to have formed by aggregation of separate grains (globules) of metal, with conservation of condensates on the grain surfaces as inclusions. The inclusions probably condensed over a significant temperature range from 1400 to 600 K. The aggregation of metal grains and formation of the nodules probably occurred simultaneously with condensation.     

Impact melting of the largest known enstatite meteorite: Al Haggounia 001, a fossil EL chondrite

Al Haggounia 001 and paired specimens (including Northwest Africa [NWA] 2828 and 7401) are part of a vesicular, incompletely melted, EL chondrite impact melt rock with a mass of ~3 metric tons. The meteorite exhibits numerous shock effects including (1) development of undulose to weak mosaic extinction in low‐Ca pyroxene; (2) dispersion of metal‐sulfide blebs within silicates causing “darkening”; (3) incomplete impact melting wherein some relict chondrules survived; (4) vaporization of troilite, resulting in S₂ bubbles that infused the melt; (5) formation of immiscible silicate and metal‐sulfide melts; (6) shock‐induced transportation of the metal‐sulfide melt to distances >10 cm; (7) partial resorption of relict chondrules and coarse silicate grains by the surrounding silicate melt; (8) crystallization of enstatite in the matrix and as overgrowths on relict silicate grains and relict chondrules; (9) crystallization of plagioclase from the melt; and (10) quenching of the vesicular silicate melt. The vesicular samples lost almost all of their metal during the shock event and were less susceptible to terrestrial weathering; in contrast, the samples in which the metal melt accumulated became severely weathered. Literature data indicate the meteorite fell ~23,000 yr ago; numerous secondary phases formed during weathering. Both impact melting and weathering altered the meteorite's bulk chemical composition: e.g., impact melting and loss of a metal‐sulfide melt from NWA 2828 is responsible for bulk depletions in common siderophile elements and in Mn (from alabandite); weathering of oldhamite caused depletions in many rare earth elements; the growth of secondary phases caused enrichments in alkalis, Ga, As, Se, and Au.     

Formation of feldspathic and metallic melts by shock in enstatite chondrite Reckling Peak A80259

Abstract— The enstatite chondrite reckling peak (rkp) a80259 contains feldspathic glass, kamacite, troilite, and unusual sets of parallel fine‐grained enstatite prisms that formed by rapid cooling of shock melts. Metallic Fe,Ni and troilite occur as spherical inclusions in feldspathic glass, reflecting the immiscible Fe‐Ni‐S and feldspathic melts generated during the impact. The Fe‐Ni‐S and feldspathic liquids were injected into fractures in coarse‐grained enstatite and cooled rapidly, resulting in thin (≤ 10 μm) semicontinuous to discontinuous veins and inclusion trails in host enstatite. Whole‐rock melt veins characteristic of heavily shocked ordinary chondrites are conspicuously absent. Raman spectroscopy shows that the feldspathic material is a glass. Elevated MgO and SiO₂ contents of the glass indicate that some enstatite and silica were incorporated in the feldspathic melt. Metallic Fe,Ni globules are enclosed by sulfide and exhibit Nienrichment along their margins characteristic of rapid crystallization from a Fe‐Ni‐S liquid. Metal enclosed by sulfide is higher in Si and P than metal in feldspathic glass and enstatite, possibly indicating lower O fugacities in metal/sulfide than in silicate domains. Fine‐grained, elongate enstatite prisms in troilite or feldspathic glass crystallized from local pyroxene melts that formed along precursor grain boundaries, but most of the enstatite in the target rock remained solid during the impact and occurs as deformed, coarsegrained crystals with lower CaO, Al₂O₃, and FeO than the fine‐grained enstatite. Reckling Peak A80259 represents an intermediate stage of shock melting between unmelted E chondrites and whole‐rock shock melts and melt breccias documented by previous workers. The shock petrogenesis of RKPA80259 reflects the extensive impact processing of the enstatite chondrite parent bodies relative to those of other chondrite types.     

A comparative study of opaque phases in Qingzhen (EH3) and MacAlpine Hills 88136 (EL3): Representatives of EH and EL parent bodies

Abstract— Opaque minerals in the Qingzhen (EH3) and MacAlpine Hills (MAC) 88136 (EL3) enstatite chondrites were studied and compared with other EH and EL chondrites. All opaque minerals usually occur in multi‐sulfide‐metal clasts and nodules in the matrix between chondrules (El Goresy et al., 1988). The higher abundance of opaque minerals, the occurrence of niningerite and various alkali‐sulfides (e.g., caswellsilverite, phases A and B, djerfisherite) are diagnostic criteria for EH chondrites, while alabandite is characteristic for EL chondrites. In addition, EH chondrites are characterized by enrichments of Si in both kamacite and perryite, and alkali elements in sphalerite and chalcopyrite. The Mn contents of daubreelite and sphalerite are lower in EH than in EL chondrites. These are consistent with lower oxygen fugacity and higher H₂S fugacity of EH than EL chondrites. In contrast, the discovery of sphalerite and Zn‐rich daubreelite in MAC 88136 indicates that their absence in EL6 chondrites is probably related to thermal metamorphism in the parent body. Schreibersite microspherules are commonly enclosed in most sulfides in Qingzhen, but are absent in MAC 88136. They were once molten, and probably predated all sulfide host phases. The petrographic setting and chemical compositions of the sulfide hosts of the schreibersite microspherules in EH3 chondrites are consistent with formation by condensation. The earliest sulfide condensates oldhamite and niningerite occupy the interiors of the clasts and nodules, whereas the rims consist of troilite and djerfisherite. In addition, in Qingzhen, some other troilite, djerfisherite and sphalerite assemblages coexist with perryite. They were produced by sulfurization of metallic Fe‐Ni in the nebula. In MAC 88136, sulfurization of Si‐bearing Fe‐Ni metal is less pronounced, and it produced troilite, schreibersite and less abundant perryite. Two kinds of normal zoning and a reverse zoning trends of niningerite, and both normal and reverse zoning of sphalerite were found in clasts and nodules in Qingzhen. The coexistence of normal and reverse zoning profiles in niningerite grains in the same meteorite strongly suggests that they formed before accretion in the parent body, because an asteroidal metamorphic or an impact event in the parent body would have erased these contrasting profiles and destroyed the textural settings. In contrast, alabandite in MAC 88136 shows only normal zoning, with the FeS content decreasing to 9.3 mol% toward troilite, indicating very slow cooling at low temperature.     

Spatial distribution of organic matter in the Bells CM2 chondrite using near‐field infrared microspectroscopy

Abstract– Distributions of organic functional groups as well as inorganic features were analyzed in the Bells (CM2) carbonaceous chondrite using near‐field infrared (NFIR) spectroscopy. NFIR spectroscopy has recently been developed to enable infrared spectral mapping beyond the optical diffraction limit of conventional Fourier transform infrared microspectroscopy. NFIR spectral mapping of the Bells 300 nm thick sections on Al plates for 7.5 × 7.5 μm² areas showed some C‐H‐rich areas which were considered to represent the organic‐rich areas. Heterogeneous distributions of organic matter as well as those of inorganic phases such as silicates (Si‐O) were observed with 1 μm spatial resolution. The NFIR mappings of aliphatic C‐H (2960 and 2930 cm^?1) and structural OH (3650 cm^?1) confirm that organic matter is associated with phyllosilicates as previously suggested. The NFIR mapping method can provide 1 μm spatial distribution of organic functional groups and their association with minerals. High local sensitivity of NFIR enables us to find organic‐rich areas and to characterize them by their aliphatic CH₂/CH₃ ratios. The aliphatic CH₂/CH₃ ratio of Bells is slightly higher than Murchison, similar to Orgueil, and lower than literature values of IDPs and cometary dust particles.     

Aqueous alteration in the matrix of the Vigarano (CV3) carbonaceous chondrite

Abstract The matrix of Vigarano, a meteorite which belongs to the reduced subgroup of the CV3 chondrites, contains small amounts (<10%) of ferrihydrite and smectite. These hydrous minerals occur together as fine fibrous intergrowths between anhydrous silicate and oxide grains. Coarser crystals of ferrihydrite fill fractures that cut matrix minerals, and smectite also lines narrow channels within olivine grains. These channels may have formed by preferential alteration of olivines along (100)-parallel defects. Formation of ferrihydrite and smectite in the matrix of Vigarano was the result of mild aqueous alteration in a low-temperature (<150 °C), oxidising parent body environment. Partial equilibration of matrix olivines indicates that alteration was followed by thermal metamorphism with a peak temperature of 400–500 °C. Mineralogically similar alteration products, which also were formed by parent body processes, have previously been described from the matrices of four CV meteorites: Bali, Grosnaja, Kaba and Mokoia, all of which belong to the oxidised subgroup. This discovery of the products of oxidative aqueous alteration in Vigarano has important consequences for understanding the chemical and thermal history of the CV class of meteorites.     

Search for isotopic anomalies in oldhamite (CaS) from unequilibrated (E3) enstatite chondrites

Abstract— The Ca isotopic compositions of 32 oldhamite (CaS) grains from the Qingzhen (EH3), MAC88136 (EL3), and Indarch (EH4) enstatite chondrites were determined by ion microprobe mass spectrometry. Also measured were the S isotopic compositions of eight oldhamite, two niningerite (MgS), and seven troilite (FeS) grains. The S isotopic compositions of all minerals are normal, but oldhamite grains of the first two meteorites exhibit apparent small ⁴⁸Ca excesses and deficits that are correlated with isotopic mass fractionation as determined from the ⁴⁰Ca-⁴⁴Ca pair. The interpretation of these results is complicated by the fact that none of the established mass fractionation laws can account for the data in the Norton County oldhamite standard. The method of analysis is carefully scrutinized for experimental artifacts. Neither interferences nor any known mass fractionation effect can satisfactorily explain the observed small deviations from normal isotopic composition. If these are truly isotopic anomalies, they are much smaller than those observed in hibonite. The nucleosynthetic origin of Ca isotopes is discussed.     

Cobalt-rich,nickel-poor metal (wairauite) in the Ningqiang carbonaceous chondrite

Abstract— A structurally ordered cubic metal grain containing ～39 wt% Co, 61 wt% Fe, and <0.6 wt% Ni (～Fe₃Co₂) was found associated with troilite and pentlandite in the matrix of the Ningqiang carbonaceous chondrite. This mineral is similar to terrestrial wairauite. Experimental data in the Fe-Co system indicate that this CsCl-type Co-rich metal is stable below 700 °C. Phase relations in the Fe-Co-Ni system show that Co cannot fractionate from Ni above 500 °C. The dominant opaque minerals of awaruite, magnetite, and pentlandite in Ningqiang suggest relatively oxidizing conditions.     

Enstatite aggregates with niningerite,heideite, and oldhamite from the Kaidun carbonaceous chondrite: Relatives of aubrites and EH chondrites?

Abstract— We studied 2 enstatite aggregates (En >99), with sizes of 0.5 and 1.5 mm, embedded in the carbonaceous matrix of Kaidun. They contain sulfide inclusions up to 650 μm in length, which consist mainly of niningerite but contain numerous grains of heideite as well as oldhamite and some secondary phases (complex Fe, Ti, S hydroxides and Ca carbonate). Both niningerite and heideite are enriched in all trace elements relative to the co‐existing enstatite except for Be and Sc. The niningerite has the highest Ca content (about 5 wt%) of all niningerites analyzed so far in any meteorite and is the phase richest in trace elements. The REE pattern is fractionated, with the CI‐normalized abundance of Lu being higher by 2 orders of magnitude than that of La, and has a strong negative Eu anomaly. Heideite is, on average, poorer in trace elements except for Zr, La, and Li. Its REE pattern is flat at about 0.5 × CI, and it also has a strong negative Eu anomaly. The enstatite is very poor in trace elements. Its Ce content is about 0.01 that of niningerite, but Li, Be, Ti, and Sc have between 0.1 and 1 × CI abundances. The preferential partitioning of typical lithophile elements into sulfides indicates highly O‐deficient and S‐dominated formation conditions for the aggregates. The minimum temperature of niningerite formation is estimated to be ?850–900 °C. The texture and the chemical characteristics of the phases in the aggregates suggest formation by aggregation and subsequent sintering before incorporation into the Kaidun breccia. The trace element data obtained for heideite, the first on record, show that this mineral, in addition to oldhamite and niningerite, is also a significant carrier of trace elements in enstatite meteorites.     

A multi‐step model for the origin of E3 (enstatite) chondrites

Abstract— It appears that the mineralogy and chemical properties of type 3 enstatite chondrites could have been established by fractionation processes (removal of a refractory component, and depletion of water) in the solar nebula, and by equilibration with nebular gas at low‐to‐intermediate temperatures (approximately 700–950 K). We describe a model for the origin of type 3 enstatite chondrites that for the first time can simultaneously account for the mineral abundances, bulk‐chemistry, and phase compositions of these chondrites by the operation of plausible processes in the solar nebula. This model, which assumes a representative nebular gas pressure of 10^?5 bar, entails three steps: (1) initial removal of 56% of the equilibrium condensed phases in a system of solar composition at 1270 K; (2) an average loss of 80–85% water vapor in the remaining gas; and (3) two different closure temperatures for the condensed phases. The first step involves a “refractory element fractionation” and is needed to account for the overall major element composition of enstatite chondrites, assuming an initial system with a solar composition. The second step, water‐vapor depletion, is needed to stabilize Si‐bearing metal, oldhamite, and niningerite, which are characteristic minerals of the enstatite chondrites. Variations in closure temperatures are suggested by the way in which the bulk chemistry and mineral assemblages of predicted condensates change with temperature, and how these parameters correlate with the observations of enstatite chondrites. In general, most phases in type 3 enstatite chondrites appear to have ceased equilibrating with nebular gas at approximately 900–950 K, except for Fe‐metal, which continued to partially react with nebular gas to temperatures as low as ～700 K.     

Shape,metal abundance,chemistry, and origin of chondrules in the Renazzo (CR) chondrite

Abstract— We used synchrotron X‐ray microtomography to image in 3‐dimensions (3D) eight whole chondrules in a ?1 cm³piece of the Renazzo (CR) chondrite at ?17 μm per volume element (voxel) edge. We report the first volumetric (3D) measurement of metal/silicate ratios in chondrules and quantify indices of chondrule sphericity. Volumetric metal abundances in whole chondrules range from 1 to 37 volume % in 8 measured chondrules and by inspection in tomography data. We show that metal abundances and metal grain locations in individual chondrules cannot be reliably obtained from single random 2D sections. Samples were physically cut to intersect representative chondrules multiple times and to verify 3D data. Detailed 2D chemical analysis combined with 3D data yield highly variable whole‐chondrule Mg/Si ratios with a supra‐chondritic mean value, yet the chemically diverse, independently formed chondrules are mutually complementary in preserving chondritic (solar) Fe/Si ratios in the aggregate CR chondrite. These results are consistent with localized chondrule formation and rapid accretion resulting in chondrule + matrix aggregates (meteorite parent bodies) that preserve the bulk chondritic composition of source regions.     

Fall,classification and cosmogenic records of the Sabrum (LL6) chondrite

Abstract— The petrographic and chemical characteristics of a fresh Indian meteorite fall at Sabrum are described. Its mean mineral composition is defined by olivine (Fa_31.4), orthopyroxene (Fs_25.1,Wo_2.0), clinopyroxene (Wo₄₅En_45.6Fs_9.4) and plagioclase (An_10.6Ab_83.6Or_5.8). The meteorite shows moderate shock features, which indicate that it belongs to the S4 category. Based on mineralogical and chemical criteria the meteorite is classified as an LL6 brecciated veined chondrite. Several cosmogenic radioisotopes (⁴⁶Sc, ⁷Be, ⁵⁴Mn, ²²Na and ²⁶Al), noble gas (He, Ne, Ar, Kr and Xe), nitrogen isotopes, and particle tracks density have been measured. Concentrations of cosmogenic ²¹Ne and ³⁸Ar indicate that its cosmic‐ray exposure age is 24.8 Ma. Small amounts of trapped Kr and Xe, consistent with petrologic class 5/6, are present. The track density in olivines is found to be (1.3 ± 0.3) × 10⁶/cm². Activities of most of the short‐lived isotopes are lower than those expected from solar cycle variation. ²²Na/²⁶Al (1.12 ± 0.02) is found to be significantly anomalous, being ?25% lower than expected from the Climax neutron monitor data. These results indicate that the cosmic‐ray flux during the terminal segment of the meteoroid orbit was low. The activities of ²⁶Al and ⁶⁰Co and the track density indicate small meteoroid size with a radius ?15 cm.     

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.