The formation of eucrites: Constraints from metal‐silicate partition coefficients

Abstract— This study explores the controls of oxygen fugacity and temperature on the solubilities of Fe, Ni, Co, Mo, and W in natural eucritic liquids to better constrain the formation of eucritic melts. The solubilities of all five elements in molten silicate in equilibrium with FeNiCo‐, FeMo‐, and FeW‐ alloys increase with increasingly oxidizing conditions and decrease with decreasing temperatures. In applying these data to formation scenarios of the eucrite parent body, we find that the siderophile element abundances in eucrites (meteoritic basalts) cannot be explained by a single‐step partialmelting process from a chondritic, metal‐containing source. The Ni content of the partial melt is too high, and the W and Mo contents are too low compared to the abundances in eucritic meteorites. But Fe, Ni, and Co concentrations in eucrites can be modeled by metal‐silicate equilibrium during more or less complete melting of the eucrite parent body with subsequent fractional crystallization of olivine and orthopyroxene. However, the computed values of Mo are still too low and those of W too high when compared with Mo and W abundances in eucritic meteorites. One possibility is that the Mo and W partition coefficients strongly depend on pressure, although the howardite‐eucrite‐diogenite (HED) parent body only had a minimal pressure gradient (maximum interior pressure = 0.1 GPa). Alternatively, sulfides may have played some role in establishing Mo abundances.     

Complexities on the acapulcoite‐lodranite parent body: Evidence from trace element distributions in silicate minerals

Abstract— The trace element distributions of individual minerals from seven acapulcoites and lodranites have been studied. Systematic differences are evident between some members of the two groups. Specifically, pyroxenes from the lodranites MacAlpine Hills (MAC) 88177 and Lewis Cliff (LEW) 88280 exhibit depletions of the rare earth elements (REE) and other incompatible trace elements (Ti, Zr, Y), relative to acapulcoite (Acapulco, Allan Hills (ALH) A81261) pyroxenes, that are consistent with the formation and removal of 15% or more silicate partial melts from these meteorites. Phosphate REE patterns in these lodranites also support this scenario. However, other members of the acapulcoite‐lodranite clan exhibit more complex trace element variations. Elephant Moraine (EET) 84302, which has been classified as transitional between the acapulcoites and lodranites, generally has trace element characteristics similar to the acapulcoites. However, its plagioclase REE compositions suggest a somewhat greater degree of metamorphism than that experienced by acapulcoites such as Acapulco and ALHA81261. Similar and elevated REE abundances in the silicate phases from acapulcoite ALHA81187 and lodranite Graves Nunataks (GRA) 95209 suggest that these two meteorites, in fact, experienced similar thermal histories. This probably included some silicate partial melting, although little melt appears to have been lost from the samples. The observed variations in the trace element abundances of these samples from the acapulcoite‐lodranite clan emphasize the complex and varied processes that have acted on their parent body. The simple bimodal classification of these meteorites based primarily on petrographic criteria, which has been used to date, appears to be inadequate to describe this diverse group of samples, as they represent a range of degrees of partial melting, both with and without accompanying melt migration. In some instances, secondary processes on the parent body, such as cryptic metasomatism, have further modified sample compositions.     

Geochemistry and 40Ar‐39Ar geochronology of impact‐melt clasts in feldspathic lunar meteorites: Implications for lunar bombardment history

Abstract— We studied 42 impact‐melt clasts from lunar feldspathic regolith breccias MacAlpine Hills (MAC) 88105, Queen Alexandra Range (QUE) 93069, Dar al Gani (DaG) 262, and DaG 400 for texture, chemical composition, and/or chronology. Although the textures are similar to the impactmelt clasts identified in mafic Apollo and Luna samples, the meteorite clasts are chemically distinct from them, having lower Fe, Ti, K, and P, thus representing previously unsampled impacts. The ⁴⁰Ar‐³⁹Ar ages on 31 of the impact melts, the first ages on impact‐melt samples from outside the region of the Apollo and Luna sampling sites, range from ～4 to ～2.5 Ga. We interpret these samples to have been created in at least six, and possibly nine or more, different impact events. One inferred impact event may be consistent with the Apollo impact‐melt rock age cluster at 3.9 Ga, but the meteorite impact‐melt clasts with this age are different in chemistry from the Apollo samples, suggesting that the mechanism responsible for the 3.9 Ga peak in lunar impact‐melt clast ages is a lunar‐wide phenomenon. No meteorite impact melts have ages more than 1s? older than 4.0 Ga. This observation is consistent with, but does not require, a lunar cataclysm.     

Petrology and geochemistry of a silicate clast from the Mount Padbury mesosiderite: Implications for metal‐silicate mixing events of mesosiderite

Abstract— Petrological and bulk geochemical studies were performed on a large silicate clast from the Mount Padbury mesosiderite. The silicate clast is composed mainly of pyroxene and plagioclase with minor amounts of ilmenite, spinel, and other accessory minerals, and it shows subophitic texture. Pyroxenes in the clast are similar to those in type 5 eucrites and could have experienced prolonged thermal metamorphism after rapid crystallization from a near‐surface melt. Ilmenite and spinel vary chemically, indicating growth under disequilibrium conditions. The clast seems to have experienced an episode of rapid reheating and cooling, possibly as a result of metal‐silicate mixing. Abundances of siderophile elements are obviously higher than in eucrites, although the clast is also extremely depleted in highly siderophile elements. The fractionated pattern can be explained by injection of Fe‐FeS melts generated by partial melting of metallic portions during metal‐silicate mixing. The silicate clast had a complex petrogenesis that could have included: 1) rapid crystallization from magma in a lava flow or a shallow intrusion; 2) prolonged thermal metamorphism to equilibrate the mineral compositions of pyroxene and plagioclase after primary crystallization; 3) metal‐silicate mixing probably caused by the impact of solid metal bodies on the surface of the mesosiderite parent body; and 4) partial melting of metal and sulfide portions (and silicate in some cases) caused by the collisional heating, which produced Fe‐FeS melts with highly fractionated siderophile elements that were injected into silicate portions along cracks and fractures.     

“New” lunar meteorites: Impact melt and regolith breccias and large‐scale heterogeneities of the upper lunar crust

Abstract— We have analyzed nine highland lunar meteorites (lunaites) using mainly INAA. Several of these rocks are difficult to classify. Dhofar 081 is basically a fragmental breccia, but much of its groundmass features a glassy‐fluidized texture that is indicative of localized shock melting. Also, much of the matrix glass is swirly‐brown, suggesting a possible regolith derivation. We interpret Dar al Gani (DaG) 400 as an extremely immature regolith breccia consisting mainly of impact‐melt breccia clasts; we interpret Dhofar 026 as an unusually complex anorthositic impact‐melt breccia with scattered ovoid globules that formed as clasts of mafic, subophitic impact melt. The presence of mafic crystalline globules in a lunar material, even one so clearly impact‐heated, suggests that it may have originated as a regolith. Our new data and a synthesis of literature data suggest a contrast in Al₂O₃‐incompatible element systematics between impact melts from the central nearside highlands, where Apollo sampling occurred, and those from the general highland surface of the Moon. Impact melts from the general highland surface tend to have systematically lower incompatible element concentration at any given Al₂O₃ concentration than those from Apollo 16. In the case of Dhofar 026, both the bulk rock and a comparatively Al‐poor composition (14 wt% Al₂O₃, 7 μg/g Sm) extrapolated for the globules, manifest incompatible element contents well below the Apollo 16 trend. Impact melts from Luna 20 (57°E) distribute more along the general highland trend than along the Apollo 16 trend. Siderophile elements also show a distinctive composition for Apollo 16 impact melts: Ni/Ir averaging ?1.8x chondritic. In contrast, lunaite impact‐melt breccias have consistently chondritic Ni/Ir. Impact melts from Luna 20 and other Apollo sites show average Ni/Ir almost as high as those from Apollo 16. The prevalence of this distinctive Ni/Ir ratio at such widely separated nearside sites suggests that debris from one extraordinarily large impact may dominate the megaregolith siderophile component of a nearside region 2300 km or more across. Highland polymict breccia lunaites and other KREEP‐poor highland regolith samples manifest a strong anticorrelation between Al₂O₃ and mg. The magnesian component probably represents the chemical signature of the Mg‐suite of pristine nonmare rocks in its most “pure” form, unaltered by the major KREEP‐assimilation that is so common among Apollo Mg‐suite samples. The average composition of the ferroan anorthositic component is now well constrained at Al₂O₃ ?29–30 wt% (implying about 17–19 wt% modal mafic silicates), in good agreement with the composition predicted for flotation crust over a “ferroan” magma ocean (Warren 1990).     

Minor and trace element concentrations in adjacent kamacite and taenite in the Krymka chondrite

We report in situ NanoSIMS siderophile minor and trace element abundances in individual Fe‐Ni metal grains in the unequilibrated chondrite Krymka (LL3.2). Associated kamacite and taenite of 10 metal grains in four chondrules and one matrix metal were analyzed for elemental concentrations of Fe, Ni, Co, Cu, Rh, Ir, and Pt. The results show large elemental variations among the metal grains. However, complementary and correlative variations exist between adjacent kamacite‐taenite. This is consistent with the unequilibrated character of the chondrite and corroborates an attainment of chemical equilibrium between the metal phases. The calculated equilibrium temperature is 446 ± 9 °C. This is concordant with the range given by Kimura et al. (2008) for the Krymka postaccretion thermal metamorphism. Based on Ni diffusivity in taenite, a slow cooling rate is estimated of the Krymka parent body that does not exceed ~1K Myr^?1, which is consistent with cooling rates inferred by other workers for unequilibrated ordinary chondrites. Elemental ionic radii might have played a role in controlling elemental partitioning between kamacite and taenite. The bulk compositions of the Krymka metal grains have nonsolar (mostly subsolar) element/Ni ratios suggesting the Fe‐Ni grains could have formed from distinct precursors of nonsolar compositions or had their compositions modified subsequent to chondrule formation events.     

Lunar meteorite regolith breccias: An in situ study of impact melt composition using LA‐ICP‐MS with implications for the composition of the lunar crust

Dar al Gani (DaG) 400, Meteorite Hills (MET) 01210, Pecora Escarpment (PCA) 02007, and MacAlpine Hills (MAC) 88104/88105 are lunar regolith breccia meteorites that provide sampling of the lunar surface from regions of the Moon that were not visited by the US Apollo or Soviet Luna sample return missions. They contain a heterogeneous clast population from a range of typical lunar lithologies. DaG 400, PCA 02007, and MAC 88104/88105 are primarily feldspathic in nature, and MET 01210 is composed of mare basalt material mixed with a lesser amount of feldspathic material. Here we present a compositional study of the impact melt and impact melt breccia clast population (i.e., clasts that were generated in impact cratering melting processes) within these meteorites using in situ electron microprobe and LA‐ICP‐MS techniques. Results show that all of the meteorites are dominated by impact lithologies that are relatively ferroan (Mg#_<70), have high Sc/Sm ratios (typically >10), and have low incompatible trace element (ITE) concentrations (i.e., typically <3.2 ppm Sm, <1.5 ppm Th). Feldspathic impact melt in DaG 400, PCA 02007, and MAC 88104/05 are similar in composition to that estimated composition for upper feldspathic lunar crust ( Korotev et al. 2003 ). However, these melt types are more mafic (i.e., less Eu, less Sr, more Sc) than feldspathic impact melts returned by the Apollo 16 mission (e.g., the group 3 and 4 varieties). Mafic impact melt clasts are common in MET 01210 and less common in PCA 02007 and MAC 88104/05. We show that unlike the Apollo mafic impact melt groups ( Jolliff 1998 ), these meteorite impact melts were not formed from melting large amounts of KREEP‐rich (typically >10 ppm Sm), High Magnesium Suite (typically >70 Mg#) or High Alkali Suite (high ITEs, Sc/Sm ratios <2) target rocks. Instead the meteorite mafic melts are more ferroan, KREEP‐poor and Sc‐rich, and represent mixing between feldspathic lithologies and low‐Ti or very low‐Ti (VLT) basalts. As PCA 02007 and MAC 88104/05 were likely sourced from the Outer‐Feldspathic Highlands Terrane our findings suggest that these predominantly feldspathic regions commonly contain a VLT to low‐Ti basalt contribution.     

Major and trace element compositions of melt particles and associated phases from the Yaxcopoil‐1 drill core,Chicxulub impact structure,Mexico

Abstract— Melt particles found at various depths in impactites from the Yaxcopoil‐1 borehole into the Chicxulub impact structure (Yucatán) have been analyzed for their major and trace element abundances. A total of 176 electron microprobe and 45 LA‐ICP‐MS analyses from eight different melt particles were investigated. The main purpose of this work was to constrain the compositions of precursor materials and secondary alteration characteristics of these melt particles. Individual melt particles are highly heterogeneous, which makes compositional categorization extremely difficult. Melt particles from the uppermost part of the impactite sequence are Ca‐ and Na‐depleted and show negative Ce anomalies, which is likely a result of seawater interaction. Various compositional groupings of melt particles are determined with ternary and binary element ratio plots involving major and trace elements. This helps distinguish the degree of alteration versus primary heterogeneity of melt phases. Comparison of the trace element ratios Sc/Zr, Y/Zr, Ba/Zr, Ba/Rb, and Sr/Rb with compositions of known target rocks provides some constraints on protolith compositions; however, the melt compositions analyzed exceed the known compositional diversity of possible target rocks. Normalized REE patterns are unique for each melt particle, likely reflecting precursor mineral or rock compositions. The various discrimination techniques indicate that the highly variable compositions are the products of melting of individual minerals or of mixtures of several minerals. Small, angular shards that are particularly abundant in units 2 and 3 represent rapidly quenched melts, whereas larger particles (>0.5 mm) that contain microlites and have fluidal, schlieric textures cooled over a protracted period. Angular, shard‐like particles with microlites in unit 5 likely crystallized below the glass transition temperature or underwent fragmentation during or after deposition.     

Major and trace element geochemistry of S‐type cosmic spherules

Micrometeorites that pass through the Earth's atmosphere undergo changes in their chemical compositions, thereby making it difficult to understand if they are sourced from the matrix, chondrules, or calcium–aluminum‐rich inclusions (CAIs). These components have the potential to provide evidence toward the understanding of the early solar nebular evolution. The variations in the major element and trace element compositions of 155 different type (scoriaceous, relict bearing, porphyritic, barred, cryptocrystalline, and glass) of S‐type cosmic spherules are investigated with the intent to decipher the parent sources using electron microprobe and laser ablation inductively coupled plasma‐mass spectrometry. The S‐type cosmic spherules appear to show a systematic depletion in volatile element contents, but have preserved their refractory trace elements. The trends in their chemical compositions suggest that the S‐type spherules comprise of components from similar parent bodies, that is, carbonaceous chondrites. Large fosteritic relict grains observed in this investigation appear to be related to the fragments of chondrules from carbonaceous chondrites. Furthermore, four spherules (two of these spherules enclose spinels and one comprised entirely of a Ca‐Al‐rich plagioclase) show enhanced trace element enrichment patterns that are drastically different from all the other 151 cosmic spherules. The information on the chemical composition and rare earth elements (REEs) on cosmic spherules suggest that the partially to fully melted ones can preserve evidences related to their parent bodies. The Ce, Eu, and Tm anomalies found in the cosmic spherules have similar behavior as that of chondrites. Distinct correlations observed between different REEs and types of cosmic spherules reflect the inherited properties of the precursors.     

Characterization of mesostasis regions in lunar basalts: Understanding late‐stage melt evolution and its influence on apatite formation

Recent studies geared toward understanding the volatile abundances of the lunar interior have focused on the volatile‐bearing accessory mineral apatite. Translating measurements of volatile abundances in lunar apatite into the volatile inventory of the silicate melts from which they crystallized, and ultimately of the mantle source regions of lunar magmas, however, has proved more difficult than initially thought. In this contribution, we report a detailed characterization of mesostasis regions in four Apollo mare basalts (10044, 12064, 15058, and 70035) in order to ascertain the compositions of the melts from which apatite crystallized. The texture, modal mineralogy, and reconstructed bulk composition of these mesostasis regions vary greatly within and between samples. There is no clear relationship between bulk‐rock basaltic composition and that of bulk‐mesostasis regions, indicating that bulk‐rock composition may have little influence on mesostasis compositions. The development of individual melt pockets, combined with the occurrence of silicate liquid immiscibility, exerts greater control on the composition and texture of mesostasis regions. In general, the reconstructed late‐stage lunar melts have roughly andesitic to dacitic compositions with low alkali contents, displaying much higher SiO₂ abundances than the bulk compositions of their host magmatic rocks. Relevant partition coefficients for apatite‐melt volatile partitioning under lunar conditions should, therefore, be derived from experiments conducted using intermediate compositions instead of compositions representing mare basalts.     

Effect of silicon on trace element partitioning in iron‐bearing metallic melts

Abstract– Despite the fact that Si is considered a potentially important metalloid in planetary systems, little is known about the effect of Si in metallic melts on trace element partitioning behavior. Previous studies have established the effects of S, C, and P, nonmetals, through solid metal/liquid metal experiments in the corresponding Fe binary systems, but the Fe‐Si system is not appropriate for similar experiments because of the high solubility of Si in solid metal. In this work, we present the results from 0.1 MPa experiments with two coexisting immiscible metallic liquids in the Fe‐S‐Si system. By leveraging the extensive available knowledge about the effect of S on trace element partitioning behavior, we explore the effect of Si. Results for 22 trace elements are presented. Strong Si avoidance behavior is demonstrated by As, Au, Ga, Ge, Sb, Sn, and Zn. Iridium, Os, Pt, Re, Ru, and W exhibit weak Si avoidance tendencies. Silicon appears to have no significant effect on the partitioning behaviors of Ag, Co, Cu, Cr, Ni, Pd, and V, all of which had similar partition coefficients over a wide range of Si liquid concentrations from Si‐free to 13 wt%. The only elements in our experiments to show evidence of a potentially weak attraction to Si were Mo and Rh. Applications of the newly determined effects of Si to problems in planetary science indicate that (1) The elements Ni, Co, Mo, and W, which are commonly used in planetary differentiation models, are minimally affected by the presence of Si in the metal, especially in comparison to other effects such as from oxygen fugacity. 2) Reduced enstatite‐rich meteorites may record a chemical signature due to Si in the metallic melts during partial melting, and if so, elements identified by this study as having strong Si avoidance may offer unique insight into unraveling the history of these meteorites.     

Contribution of early impact events to metal‐silicate separation,thermal annealing,and volatile redistribution: Evidence in the Pułtusk H chondrite

Three‐dimensional X‐ray tomographic reconstructions and petrologic studies reveal voluminous accumulations of metal in Pu?tusk H chondrite. At the contact of these accumulations, the chondritic rock is enriched in troilite. The rock contains plagioclase‐rich bands, with textures suggesting crystallization from melt. Unusually large phosphates are associated with the plagioclase and consist of assemblages of merrillite, and fluorapatite and chlorapatite. The metal accumulations were formed by impact melting, rapid segregation of metal‐sulfide melt and the incorporation of this melt into the fractured crater basement. The impact most likely occurred in the early evolution of the H chondrite parent body, when post‐impact heat overlapped with radiogenic heat. This enabled slow cooling and separation of the metallic melt into metal‐rich and sulfide‐rich fractions. This led to recrystallization of chondritic rock in contact with the metal accumulations and the crystallization of shock melts. Phosphorus was liberated from the metal and subsumed by the silicate shock melt, owing to oxidative conditions upon slow cooling. The melt was also a host for volatiles. Upon further cooling, phosphorus reacted with silicates leading to the formation of merrillite, while volatiles partitioned into the residual halogen‐rich, dry fluid. In the late stages, the fluid altered merrillite to patchy Cl/F‐apatite. The above sequence of alterations demonstrates that impact during the early evolution of chondritic parent bodies might have contributed to local metal segregation and silicate melting. In addition, postshock conditions supported secondary processes: compositional/textural equilibration, redistribution of volatiles, and fluid alterations.     

Petrology and geochemistry of feldspathic impact‐melt breccia Abar al' Uj 012, the first lunar meteorite from Saudi Arabia

Abar al' Uj (AaU) 012 is a clast‐rich, vesicular impact‐melt (IM) breccia, composed of lithic and mineral clasts set in a very fine‐grained and well‐crystallized matrix. It is a typical feldspathic lunar meteorite, most likely originating from the lunar farside. Bulk composition (31.0 wt% Al₂O₃, 3.85 wt% FeO) is close to the mean of feldspathic lunar meteorites and Apollo FAN‐suite rocks. The low concentration of incompatible trace elements (0.39 ppm Th, 0.13 ppm U) reflects the absence of a significant KREEP component. Plagioclase is highly anorthitic with a mean of An_96.9Ab_3.0Or_0.1. Bulk rock Mg# is 63 and molar FeO/MnO is 76. The terrestrial age of the meteorite is 33.4 ± 5.2 kyr. AaU 012 contains a ~1.4 × 1.5 mm² exotic clast different from the lithic clast population which is dominated by clasts of anorthosite breccias. Bulk composition and presence of relatively large vesicles indicate that the clast was most probably formed by an impact into a precursor having nonmare igneous origin most likely related to the rare alkali‐suite rocks. The IM clast is mainly composed of clinopyroxenes, contains a significant amount of cristobalite (9.0 vol%), and has a microcrystalline mesostasis. Although the clast shows similarities in texture and modal mineral abundances with some Apollo pigeonite basalts, it has lower FeO and higher SiO₂ than any mare basalt. It also has higher FeO and lower Al₂O₃ than rocks from the FAN‐ or Mg‐suite. Its lower Mg# (59) compared to Mg‐suite rocks also excludes a relationship with these types of lunar material.     

Mineralogy,petrology, and shock history of lunar meteorite Sayh al Uhaymir 300: A crystalline impact‐melt breccia

Abstract— Sayh al Uhaymir (SaU) 300 comprises a microcrystalline igneous matrix (grain size <10 μm), dominated by plagioclase, pyroxene, and olivine. Pyroxene geothermometry indicates that the matrix crystallized at ?1100 °C. The matrix encloses mineral and lithic clasts that record the effects of variable levels of shock. Mineral clasts include plagioclase, low‐ and high‐Ca pyroxene, pigeonite, and olivine. Minor amounts of ilmenite, FeNi metal, chromite, and a silica phase are also present. A variety of lithic clast types are observed, including glassy impact melts, impact‐melt breccias, and metamorphosed impact melts. One clast of granulitic breccia was also noted. A lunar origin for SaU 300 is supported by the composition of the plagioclase (average An₉₅), the high Cr content in olivine, the lack of hydrous phases, and the Fe/Mn ratio of mafic minerals. Both matrix and clasts have been locally overprinted by shock veins and melt pockets. SaU 300 has previously been described as an anorthositic regolith breccia with basaltic components and a granulitic matrix, but we here interpret it to be a polymict crystalline impact‐melt breccia with an olivine‐rich anorthositic norite bulk composition. The varying shock states of the mineral and lithic clasts suggest that they were shocked to between 5–28 GPa (shock stages S1–S2) by impact events in target rocks prior to their inclusion in the matrix. Formation of the igneous matrix requires a minimum shock pressure of 60 GPa (shock stage >S4). The association of maskelynite with melt pockets and shock veins indicates a subsequent, local 28–45 GPa (shock stage S2–S3) excursion, which was probably responsible for lofting the sample from the lunar surface. Subsequent fracturing is attributed to atmospheric entry and probable breakup of the parent meteor.     

Trace element concentrations in the Mexico‐Belize ejecta layer: A link between the Chicxulub impact and the global Cretaceous‐Paleogene boundary

Abstract— Four exposures of Chicxulub impact ejecta along the Mexico‐Belize border have been sampled and analyzed for major and trace element abundances. The ejecta deposits consist of a lower spheroid bed, containing clay and dolomite spheroids, and an upper diamictite bed with boulders and clasts of limestone and dolomite. The matrix of both beds is composed of clay and micritic dolomite. The rare earth element (REE) compositions in the matrix of both units show strong similarities in concentrations and pattern. Furthermore, the Zr/TiO₂ scatter plot shows a linear correlation indicating one source. These results indicate that the basal spheroid bed has the same source and was generated during the same event as the overlying diamictite bed, which lends support to a single‐impact scenario for the Albion Formation ejecta deposits. The elevated concentrations of non‐meteoritic elements such as Sb, As, U, and Zn in the matrix of the lower spheroid bed are regarded to have been derived from the sedimentary target rocks at the Chicxulub impact site. The positive Eu and Ce anomalies in clay concretion and in the matrix of the lower part of the spheroid bed in Albion Island quarry is probably related to processes involved in the impact, such as high temperature and oxidizing conditions. Analogous trace element anomalies have been reported from the distal Cretaceous‐Paleogene (K/T) boundary clay layer at different sites. Thus, the trace element signals, reported herein, are regarded to support a genetic link between the Chicxulub impact, the ejecta deposits along the Mexico‐Belize border, and the global K/T boundary layer.     

Major and trace element characteristics of impactites from the Yaxcopoil‐1 borehole,Chicxulub structure,Mexico

Abstract— Approximately 100 m of impactites were retrieved from the ICDP borehole Yaxcopoil‐1 (Yax‐1), located ～60 km south‐southwest from the center of the Chicxulub impact crater on the Yucatán Peninsula of Mexico. Here, we characterize and discuss this impact breccia interval according to its geochemical characteristics. Chemical analysis of samples from all five recognized breccia units reveals that the impactites are of heterogeneous composition with regard to both major and trace elements at the single sample (8–16 cm³) scale. This is primarily due to a strong mixing relationship between carbonate and silicate fractions. However, averaged compositions for suevitic units 1 to 3 are similar, and the silicate fraction (after removal of the carbonate component) indicates thorough mixing and homogenization. Analysis of the green melt breccia horizon, unit 4, indicates that it contains a distinct mafic component. Large brown melt particles (in units 2, 3, and 4) represent a mixture of feldspathic and mafic components, with high CaO abundances. Unit 5 shows the greatest compositional diversity, with highly variable abundances of SiO₂, CaO, and MgO. Inter‐sample heterogeneity is the result of small sample size combined with inherent heterogeneous lithological compositions, highly variable particle size of melt and lithic components, and post‐depositional alteration. In contrast to samples from the Y6 borehole from closer to the center of the structure, Yax‐1 impactites have a strong carbonate component. Elevated loss on ignition, Rb, and Cs contents in the upper two impactite units indicate strong interaction with seawater. The contents of the siderophile elements, including Ni, Co, Ir, and Cr, do not indicate the presence of a significant extraterrestrial component in the Yax‐1 impactites.     

Partitioning of Ca and Al between forsterite and silicate melt in dynamic systems with implications for the origin of Ca,Al‐rich forsterites in primitive meteorites

Abstract— We report the results of dynamic crystallization experiments that were specifically designed to study the dependence of Ca and Al partitioning between forsterite and melt in rapidly cooling Caand Al‐rich melts. The partitioning of Ca between olivine and silicate melt is found to be independent of the cooling rate within the range of 1.5 to 1000°C/hr and at CaO contents of up to 25 wt%. Within analytical uncertainty, our data plot on the equilibrium partitioning curve obtained by Libourel (1999). The partitioning behavior of Al at high cooling rates is more complex. Aluminum is much more heterogenously distributed in the olivine and the co‐existing melt than Ca. But, no systematic trend of Al partition coefficient with cooling rate is observed. We apply the results of the experiments to the formation of meteoritic forsterites with relatively high contents of Ca and Al. Although these forsterites are found frequently inside chondrules, the Ca contents of their host chondrules are far too low to crystallize these high Ca‐forsterites. This is also true for very rapid cooling of chondrule melts. The parental melt of these forsterites requires CaO contents above 20 wt%.     

The non‐igneous genesis of angrites: Support from trace element distribution between phases in D'Orbigny

Abstract— D'Orbigny is an exceptional angrite. Chemically, it resembles other angrites such as Asuka‐881371, Sahara 99555, Lewis Cliff (LEW) 87051, and LEW 86010, but its structure and texture are peculiar. It has a compact and porous lithology, abundant glasses, augite‐bearing druses, and chemical and mineralogical properties that are highly unusual for igneous rocks. Our previous studies led us to a new view on angrites: they can possibly be considered as CAIs that grew to larger sizes than the ones we know from carbonaceous chondrites. Thus, angrites may bear a record of rare and special conditions in some part of the early solar nebula. Here we report trace element contents of D'Orbigny phases. Trace element data were obtained from both the porous and the compact part of this meteorite. We have confronted our results with the popular igneous genetic model. According to this model, if all phases of D'Orbigny crystallized from the same system, as an igneous origin implies, a record of this genesis should be expressed in the distribution of trace elements among early and late phases. Our results show that the trace element distribution of the two contemporaneous phases olivine and plagioclase, which form the backbone of the rock, seem to require liquids of different composition. Abundances of highly incompatible elements in all olivines, including the megacrysts, indicate disequilibrium with the bulk rock and suggest liquids very rich in these elements (>10,000 x CI), which is much richer than any fractional crystallization could possibly produce. In addition, trace element contents of late phases are incompatible with formation from the bulk system's residual melt. These results add additional severe constraints to the many conflicts that existed previously between an igneous model for the origin of angrites and the mineralogical and chemical observations. This new trace element content data, reported here, corroborate our previous results based on the shape, structure, mineralogy, chemical, and isotopic data of the whole meteorite, as well as on a petrographic and chemical composition study of all types of glasses and give strength to a new genetic model that postulates that D'Orbigny (and possibly all angrites) could have formed in the solar nebula under changing redox conditions, more akin to chondritic constituents (e.g., CAIs) than to planetary differentiated rock.     

Production rates of cosmogenic helium‐3, neon‐21, and neon‐22 in ordinary chondrites and the lunar surface

Abstract— The production of ³He, ²¹Ne, and ²²Ne in meteoroids of various sizes and in the lunar surface was investigated. The LAHET code system, a purely physical model for calculating cosmic‐ray particle fluxes, was used to simulate cosmic‐ray particle interactions with extraterrestrial matter. We discuss the depth and size dependence of the shielding parameter ²²Ne/²¹Ne, which is used for reconstruction of pre‐atmospheric sizes, depth, and exposure histories. The ²²Ne/²¹Ne ratio decreases with increasing depth or pre‐atmospheric size but then increases with depth in very large objects. This increase with depth in the ²²Ne/²¹Ne ratio means that this ratio is a poor indicator of shielding in some large objects. The dependence of ³He/²¹Ne as function of ²²Ne/²¹Ne was also calculated, and differences between the calculations and the Bern line are discussed.     

Refractory calcium‐aluminum‐rich inclusions and aluminum‐diopside‐rich chondrules in the metal‐rich chondrites Hammadah al Hamra 237 and Queen Alexandra Range 94411

Abstract— The metal‐rich chondrites Hammadah al Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627, contain relatively rare (<1 vol%) calcium‐aluminum‐rich inclusions (CAIs) and Al‐diopside‐rich chondrules. Forty CAIs and CAI fragments and seven Al‐diopside‐rich chondrules were identified in HH 237 and QUE 94411/94627. The CAIs, ～50–400 μm in apparent diameter, include (a) 22 (56%) pyroxene‐spinel ± melilite (+forsterite rim), (b) 11 (28%) forsterite‐bearing, pyroxene‐spinel ± melilite ± anorthite (+forsterite rim) (c) 2 (5%) grossite‐rich (+spinel‐melilite‐pyroxene rim), (d) 2 (5%) hibonite‐melilite (+spinel‐pyroxene ± forsterite rim), (e) 1 (2%) hibonite‐bearing, spinel‐perovskite (+melilite‐pyroxene rim), (f) 1 (2%) spinel‐melilite‐pyroxene‐anorthite, and (g) 1 (2%) amoeboid olivine aggregate. Each type of CAI is known to exist in other chondrite groups, but the high abundance of pyroxene‐spinel ± melilite CAIs with igneous textures and surrounded by a forsterite rim are unique features of HH 237 and QUE 94411/94627. Additionally, oxygen isotopes consistently show relatively heavy compositions with Δ¹⁷O ranging from ?6%0 to ?10%0 (1σ = 1.3%0) for all analyzed CAI minerals (grossite, hibonite, melilite, pyroxene, spinel). This suggests that the CAIs formed in a reservoir isotopically distinct from the reservoir(s) where “normal”, ¹⁶O‐rich (Δ¹⁷O < ?20%0) CAIs in most other chondritic meteorites formed. The Al‐diopside‐rich chondrules, which have previously been observed in CH chondrites and the unique carbonaceous chondrite Adelaide, contain Al‐diopside grains enclosing oriented inclusions of forsterite, and interstitial anorthitic mesostasis and Al‐rich, Ca‐poor pyroxene, occasionally enclosing spinel and forsterite. These chondrules are mineralogically similar to the Al‐rich barred‐olivine chondrules in HH 237 and QUE 94411/94627, but have lower Cr concentrations than the latter, indicating that they may have formed during the same chondrule‐forming event, but at slightly different ambient nebular temperatures. Aluminum‐diopside grains from two Al‐diopside‐rich chondrules have O‐isotopic compositions (Δ¹⁷O ? ?7 ± 1.1 %0) similar to CAI minerals, suggesting that they formed from an isotopically similar reservoir. The oxygen‐isotopic composition of one Ca, Al‐poor cryptocrystalline chondrule in QUE 94411/94627 was analyzed and found to have Δ¹⁷O ? ?3 ± 1.4%0. The characteristics of the CAIs in HH 237 and QUE 94411/94627 are inconsistent with an impact origin of these metal‐rich meteorites. Instead they suggest that the components in CB chondrites are pristine products of large‐scale, high‐temperature processes in the solar nebula and should be considered bona fide chondrites.