Geochemical zoning and magnetic mineralogy at Fe,Ni‐alloy–troilite interfaces of three iron meteorites from Morasko,Coahuila II,and Mundrabilla

We combined high‐resolution and space‐resolved elemental distribution with investigations of magnetic minerals across Fe,Ni‐alloy and troilite interfaces for two nonmagmatic (Morasko and Mundrabilla) IAB group iron meteorites and an octahedrite found in 1993 in Coahuila/Mexico (Coahuila II) preliminarily classified on Ir and Au content as IIAB group. The aim of this study was to elucidate the crystallization and thermal history using gradients of the siderophile elements Ni, Co, Ge, and Ga and the chalcophile elements Cr, Cu, and Se with a focus on magnetic minerals. The Morasko and Coahuila II meteorite show a several mm‐thick carbon‐ and phosphorous‐rich transition zone between Fe,Ni‐alloy and troilite, which is characterized by magnetic cohenite and nonmagnetic or magnetic schreibersite. At Morasko, these phases have a characteristic trace element composition with Mo enriched in cohenite. In both Morasko and Coahuila II, Ni is enriched in schreibersite. The minerals have crystallized from immiscible melts, either by fractional crystallization and C‐ and P‐enrichment in the melt, or by partial melting at temperatures slightly above the eutectic point. During crystallization of Mundrabilla, the field of immiscibility was not reached. Independent of meteorite group and cooling history, the magnetic mineralogy (daubreelite, cohenite and/or schreibersite, magnetite) is very similar to the troilite (and transition zone) for all three investigated iron meteorites. If these minerals can be separated from the metal, they might provide important information about the early solar system magnetic field. Magnetite is interpreted as a partial melting or a terrestrial weathering product of the Fe,Ni‐alloy under oxidizing conditions.     

The Twannberg (Switzerland) IIG iron meteorites: Mineralogy,chemistry, and CRE ages

Abstract— The original mass (15915 g) of the Twannberg IIG (low Ni‐, high P) iron was found in 1984. Five additional masses (12 to 2488 g) were recovered between 2000 and 2007 in the area. The different masses show identical mineralogy consisting of kamacite single crystals with inclusions of three types of schreibersite crystals: cm‐sized skeletal (10.5% Ni), lamellar (17.2% Ni), and 1–3 × 10 μm‐sized microprismatic (23.9% Ni). Masses I and II were compared in detail and have virtually identical microstructure, hardness, chemical composition, cosmic‐ray exposure (CRE) ages, and ¹⁰Be and ²⁶Al activities. Bulk concentrations of 5.2% Ni and 2.0% P were calculated. The preatmospheric mass is estimated to have been at least 11,000 kg. The average CRE age for the different Twannberg samples is 230 ± 50 Ma. Detrital terrestrial mineral grains in the oxide rinds of the three larger masses indicate that they oxidized while they were incorporated in a glacial till deposited by the Rhône glacier during the last glaciation (Würm). The find location of mass I is located at the limit of glaciation where the meteorite may have deposited after transport by the glacier over considerable distance. All evidence indicates pairing of the six masses, which may be part of a larger shower as is indicated by the large inferred pre‐atmospheric mass.     

An investigation of the behavior of Cu and Cr during iron meteorite crystallization

Abstract— The measured Cu and Cr contents in magmatic iron meteorites appear to contradict the behavior predicted by experimental fractional crystallization studies currently available. To investigate the origin of Cu and Cr concentrations observed in these meteorites, a thorough set of solid metal/liquid metal experiments were conducted in the Fe‐Ni‐S system. In addition to Cu and Cr, partitioning values were also determined for As, Au, Bi, Co, Mo, Ni, Pb, Rh, Ru, Sb, Sn, V, and Zn from the experiments. Experimental results for Cu and Cr showed similar chalcophile partitioning behavior, whereas these elements have differently sloped trends within magmatic iron meteorite groups. Thus, fractional crystallization alone cannot control both the Cu and Cr concentrations in these iron meteorite groups. A simple fractional crystallization model based on our experimental Cu partitioning results was able to match the Cu versus Au trend observed in the S‐poor IVB iron meteorite group but not the decreasing Cu versus Au trends in the IIAB and IIIAB groups or the unique S‐shaped Cu versus Au trend in the IVA group. However, the crystallization model calculations were found to be very sensitive to the specific choice for the mathematical expression of D(Cu), suggesting that any future refinement of the parameterization of D(Cu) should include a reassessment of the Cu fractional crystallization trends. The Cr versus Au trends in magmatic iron meteorite groups are steeper than those of Cu and not explained by fractional crystallization. Other influences, such as the removal of chromite from the crystallizing system or sampling biases during iron meteorite compositional analyses, are likely responsible for the Cr trends in magmatic iron meteorite groups.     

The effect of Ni on element partitioning during iron meteorite crystallization

Abstract— ‐Iron meteorites exhibit a large range in Ni concentrations, from only 4% to nearly 60%. Most previous experiments aimed at understanding the crystallization of iron meteorites have been conducted in systems with about 10% Ni or less. We performed solid metal/liquid metal experiments to determine the effect of Ni on partition coefficients for 20 trace elements pertinent to iron meteorites. Experiments were conducted in both the end‐member Ni‐S system as well as in the Fe‐Ni‐S system with intermediate Ni compositions applicable to high‐Ni iron meteorites. The Ni content of the system affects solid metal/liquid metal partitioning behavior. For a given S concentration, partition coefficients in the Ni‐S system can be over an order of magnitude larger than in the Fe‐S system. However, for compositions relevant to even the most Ni‐rich iron meteorites, the effect of Ni on partitioning behavior is minor, amounting to less than a factor of two for the majority of trace elements studied. Any effect of Ni also appears minor when it is compared to the large influence S has on element partitioning behavior. Thus, we conclude that in the presence of an evolving S‐bearing metallic melt, crystallization models can safely neglect effects from Ni when considering the full range of iron meteorite compositions.     

Experimental determination of partitioning in the Fe‐Ni system for applications to modeling meteoritic metals

Experimental trace element partitioning values are often used to model the chemical evolution of metallic phases in meteorites, but limited experimental data were previously available to constrain the partitioning behavior in the basic Fe‐Ni system. In this study, we conducted experiments that produced equilibrium solid metal and liquid metal phases in the Fe‐Ni system and measured the partition coefficients of 25 elements. The results are in good agreement with values modeled from IVB iron meteorites and with the limited previous experimental data. Additional experiments with low levels of S and P were also conducted to help constrain the partitioning behaviors of elements as a function of these light elements. The new experimental results were used to derive a set of parameterization values for element solid metal–liquid metal partitioning behavior in the Fe‐Ni‐S, Fe‐Ni‐P, and Fe‐Ni‐C ternary systems at 0.1 MPa. The new parameterizations require that the partitioning behaviors in the light‐element–free Fe‐Ni system are those determined experimentally by this study, in contrast to previous parameterizations that allowed this value to be determined as a best‐fit parameter. These new parameterizations, with self‐consistent values for partitioning in the endmember Fe‐Ni system, provide a valuable resource for future studies that model the chemical evolution of metallic phases in meteorites.     

Effects of liquid immiscibility on trace element fractionation in magmatic iron meteorites: A case study of group IIIAB

Abstract— Magmatic iron meteorites are generally agreed to represent metal that crystallized in asteroidal cores from a large pool of liquid. Estimates suggest that the metallic liquid contained significant amounts of S and P, both of which are incompatible and exert a strong effect on trace element partitioning. In tandem, S and P are also prone to cause immiscibility between sulfide liquid and P-rich metal liquid. The liquid immiscibility field occupies ～70% of the portion of the Fe-Ni-S-P system in which Fe is the first phase to crystallize. In spite of this, previous fractional crystallization models have taken into account only one liquid phase and have encountered significant discrepancies between the meteorite data and model values for the key elements Ni, Ir, Ga, Ge and Au at even moderate degrees of fractionation. For the first time, a model for trace element partitioning between immiscible liquids in the Fe-Ni-S-P system is presented in order to assess the effects on fractionation in magmatic iron meteorite groups. The onset of liquid immiscibility causes a significant change in the enrichment patterns of S and P in both liquids; so elements with contrasting partitioning behavior will show trends deviating clearly from one-liquid trends. A trend recorded in the solid metal will either be a smooth curve as long as equilibrium is maintained between the two liquids or the trend may diverge into a field limited by two extreme curves depending on the degree of disequilibrium. Bulk initial liquids for most magmatic groups have S/P (wt%) ratios well below 25. In these cases and due to the constitution of the Fe-Ni-S-P system, most of the metal will crystallize from the rapidly decreasing volume of metal liquid and only a subordinate amount from the sulfide liquid. Because of the strong extraction of P into the metal liquid, P will have a much larger influence on trace element partitioning than a low initial P content might suggest. My model calculations suggest that liquid immiscibility played a significant role during the solidification of the IIIAB parent body's core. The two-liquid model reproduces the IIIAB trends more closely than previous one-liquid models and can account for: (a) the general widening of the IIIAB trend with increasing Ni and decreasing Ir contents, (b) the occurrence of high-Ni members that are not strongly depleted in Ir, Ga and Ge; and (c) an upper limit at ～11 wt% Ni where the metal liquid was almost consumed.     

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.     

Crystallization of magmatic iron meteorites: The effects of phosphorus and liquid immiscibility

Abstract— Magmatic iron meteorites are commonly thought to have formed by fractional crystallization of the metallic cores of asteroid‐sized bodies. As fractional crystallization proceeds, light elements such as P and S become enriched in the molten portion of the core. The light element content of the metallic liquid influences the partitioning behavior of trace elements and may cause liquid immiscibility to occur. The elemental trends observed in magmatic iron meteorites may have been affected by both of these processes. We have examined experimentally the effect of P on the solid‐metal‐liquid‐metal partitioning behavior of Ag and Pd, Re and Os, two element pairs used to date iron meteorite processes. Phosphorus has no effect on the partition coefficient of either Ag or Pd, which are incompatible and identical within experimental error. Compatible Re and Os also have identical partitioning behavior, within experimental error, and show increasing compatibility in the solid metal with increasing P content of the metallic liquid. Including the effects of both S and P on the partitioning behavior of Re and Os, simple fractional crystallization calculations can reproduce the large variation of Re and Os concentrations observed in four magmatic iron meteorite groups but have difficulty matching the later crystallizing portions of the trends. We have also conducted experiments with three phases—solid metal and two immiscible metallic liquids—to determine the location of the liquid immiscibility field near conditions thought to be relevant to magmatic iron meteorites. Our results show a significantly smaller liquid immiscibility field as compared to the previously published Fe‐P‐S phase diagram. Our revised phase diagram suggests that liquid immiscibility was encountered during the crystallization of asteroidal cores, but much later during the crystallization process than predicted by the previously published diagram.     

An experimental test of Henry's Law in solid metal‐liquid metal systems with implications for iron meteorites

Abstract— Experimental solid metal‐liquid metal partition coefficients have been used to model the crystallization of magmatic iron meteorites and understand the evolution of asteroid cores. However, the majority of the partitioning experiments have been conducted with trace elements doped at levels that are orders of magnitude higher than measured in iron meteorites. Concern about Henry's Law and the unnatural doping levels have been cited as one reason that two recent iron meteorite studies have dismissed the experimental partition coefficients in their modeling. Using laser ablation ICP‐MS analysis, this study reports experimentally determined solid metal‐liquid metal trace element partition coefficients from runs doped down to the levels occurring in iron meteorites. The analyses for 12 trace elements (As, Co, Cr, Cu, Ga, Ge, Ir, Os, Pd, Pt, Re, and W) show no deviations from Henry's Law, and these results support decades of experimental work in which the partition coefficients were assumed to be independent of trace element concentration. Further, since our experiments are doped with natural levels of trace elements, the partitioning results are directly applicable to iron meteorites and should be used when modeling their crystallization. In contrast, our new Ag data are inconsistent with previous studies, suggesting the high Ag‐content in previous studies may have influenced the measured Ag partitioning behavior.     

METAL AND SCHREIBERSITE IN MAYO BELWA,AN ENSTATITE ACHONDRITE

The Mayo Belwa meteorite (an aubrite) contains discrete metal grains ranging in size from less than 1 μm to 300 μm across, and schreibersites up to 25 μm across. Intergrowths of metal and schreibersite also occur. These phases are distributed heterogeneously throughout the meteorite and are present both in the fine-grained matrix and within silicate crystals. The concentrations of the elements Ni, Fe, Si, Co, P, were determined in grains larger than 4 μm across. Most metal grains have 1–8% Ni, the total range being 0.8–23.5% Ni. The 1–8% Ni metal may be sub-divided into two compositional groups, one relatively compact, having 1–3.8% Ni, 0.1-0.3% Si; the second having a much greater range in both Ni and Si (～ 4–12%, 0.1-1.2% respectively). There is no zonation in the Si contents of individual grains. Neither the size of the grains nor their environment correlates with their Ni or Si contents, though there is a tendency for low Ni, low Si metal to be within enstatite crystals. Schreibersite (8–14.4% Ni) occurs as isolated grains or associated with low-Ni metal; it generally contains less than 500 ppm Si. The wide range in the Ni contents of the metal distinguishes it from the metal of the E-chondrites, and argues against an E-chondrite source for this metal.     

Petrogenesis of anomalous Queen Alexandra Range enstatite meteorites and their relation to enstatite chondrites,primitive enstatite achondrites,and aubrites

Queen Alexandra Range (QUE) meteorite 94204 is an anomalous enstatite meteorite whose petrogenesis has been ascribed to either partial melting or impact melting. We studied the meteorite pairs QUE 94204, 97289/97348, 99059/99122/99157/99158/99387, and Yamato (Y)‐793225; these were previously suggested to represent a new grouplet. We present new data for mineral abundances, mineral chemistries, and siderophile trace element compositions (of Fe,Ni metal) in these meteorites. We find that the texture and composition of Y‐793225 are related to EL6, and that this meteorite is unrelated to the QUEs. The mineralogy and siderophile element compositions of the QUEs are consistent with petrogenesis from an enstatite chondrite precursor. We caution that potential re‐equilibration during melting and recrystallization of enstatite chondrite melt‐rocks make it unreliable to use mineral chemistries to assign a specific parent body affinity (i.e., EH or EL). The QUEs have similar mineral chemistries among themselves, while slight variations in texture and modal abundances exist between them. They are dominated by inclusion‐bearing millimeter‐sized enstatite (average En_99.1–99.5) with interstitial spaces filled predominantly by oligoclase feldspar (sometimes zoned), kamacite (Si approximately 2.4 wt%), troilite (≤2.4 wt% Ti), and cristobalite. Siderophile elements that partition compatibly between solid metal and liquid metal are not enriched like in partial melt residues Itqiy and Northwest Africa (NWA) 2526. We find that the modal compositions of the QUEs are broadly unfractionated with respect to enstatite chondrites. We conclude that a petrogenesis by impact melting, not partial melting, is most consistent with our observations.     

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.     

Portales Valley: Petrology of a metallic‐melt meteorite breccia

Abstract— Portales Valley (PV) is an unusual metal‐veined meteorite that has been classified as an H6 chondrite. It has been regarded either as an annealed impact melt breccia, as a primitive achondrite, or as a meteorite with affinities to silicated iron meteorites. We studied the petrology of PV using a variety of geochemical‐mineralogical techniques. Our results suggest that PV is the first well‐documented metallic‐melt meteorite breccia. Mineral‐chemical and other data suggest that the protolith to PV was an H chondrite. The composition of FeNi metal in PV is somewhat fractionated compared to H chondrites and varies between coarse vein and silicate‐rich portions. It is best modeled as having formed by partial melting at temperatures of ?940–1150 °C, with incomplete separation of solid from liquid metal. Solid metal concentrated in the coarse vein areas and S‐bearing liquid metal concentrated in the silicate‐rich areas, possibly as a result of a surface energy effect. Both carbon and phosphorus must have been scavenged from large volumes and concentrated in metallic liquid. Graphite nodules formed by crystallization from this liquid, whereas phosphate formed by reaction between P‐bearing metal and clinopyroxene components, depleting clinopyroxene throughout much of the meteorite and growing coarse phosphate at metal‐silicate interfaces. Some phosphate probably crystallized from P‐bearing liquids, but most probably formed by solid‐state reaction at ?975‐725 °C. Phosphate‐forming and FeO‐reduction reactions were widespread in PV and entailed a change in the mineralogy of the stony portion on a large scale. Portales Valley experienced protracted annealing from supersolidus to subsolidus temperatures, probably by cooling at depth within its parent body, but the main differences between PV and H chondrites arose because maximum temperatures were higher in PV. A combination of a relatively weak shock event and elevated pre‐shock temperatures probably produced the vein‐and‐breccia texture, with endogenic heating being the main heat source for melting, and with stress waves from an impact event being an essential trigger for mobilizing metal. Portales Valley is best classified as an H7 metallic‐melt breccia of shock stage S1. The meteorite is transitional between more primitive (chondritic) and evolved (achondrite, iron) meteorite types and offers clues as to how differentiation could have occurred in some asteroidal bodies.     

Shock‐thermal history of the Agoudal (IIAB) iron meteorite from microstructural studies

The Agoudal IIAB iron meteorite exhibits only kamacite grains (~6 mm across) without any taenite. The kamacite is homogeneously enriched with numerous rhabdite inclusions of different size, shape, and composition. In some kamacite domains, this appears frosty due to micron‐scale rhabdite inclusions (~5 to 100 μm) of moderate to high Ni content (~26 to 40 wt%). In addition, all the kamacite grains in matrix are marked with a prominent linear crack formed during an atmospheric break‐up event and subsequently oxidized. This feature, also defined by trails of lowest Ni‐bearing (mean Ni: 23 wt%) mm‐scale rhabdite plates (fractured and oxidized) could be a trace of a pre‐existing γ–α interface. Agoudal experienced a very slow rate of primary cooling ~4 °C Ma^?1 estimated from the binary plots of true rhabdite width against corresponding Ni wt% and the computed cooling rate curves after Randich and Goldstein (1978). Chemically, Agoudal iron (Ga: 54 ppm; Ge: 140 ppm; Ir: 0.03 ppm) resembles the Ainsworth iron, the coarsest octahedrite of the IIAB group. Agoudal contains multiple sets of Neumann bands that are formed in space and time at different scales and densities due to multiple impacts with shock magnitude up to 130 kb. Signatures of recrystallization due to postshock low temperature mild reheating at about 400 °C are also locally present.     

The parameterization of solid metal‐liquid metal partitioning of siderophile elements

Abstract— Many solar system processes involve a metallic liquid, and the composition of the metallic liquid, such as the liquid's concentrations of S, P, and C, will influence the partitioning of elements during such processes. We present a method for parameterizing solid metal‐liquid metal partition coefficients for siderophile (metal‐loving) elements as a function of the metallic liquid composition. Our parameterization method is based on an older theory of Jones and Malvin (1990), which stated that the metallic liquid is composed of metal and non‐metal‐bearing domains, and the domains are the dominant influence on the partitioning behavior. By revising the means by which the metal domains are calculated, our revised parameterization method is able to match experimental partitioning data from the Fe‐Ni‐S, Fe‐Ni‐P, Fe‐Ni‐S‐P, and Fe‐Ni‐C systems. Mathematical expressions were derived for the solid metal‐liquid metal partitioning of 13 siderophile elements. Elements that are chalcophile (S‐loving), P‐loving, or C‐loving prefer the non‐metal‐bearing domains in the metallic liquid and, consequently, aren't fit by the parameterization method presented here. Possible applications for our parameterization method include modeling the crystallization of iron meteorites, planetary differentiation, and the solidification of Earth's inner core.     

Noble gases in metal and schreibersite of the Acuña (IIIAB) iron meteorite

Abstract— We measured abundances and isotopic compositions of noble gases in metal and schreibersite of the Acuña (IIIAB) iron meteorite. The concentrations of noble gases in Acuña metal are very low compared to those reported so far for other iron meteorites. The isotopic ratios of He, Ne and Ar indicate that they are mostly of cosmogenic origin. Cosmogenic components are even present in Kr and Xe, which could not have been produced from Fe, Ni and P and are probably due to the spallation of trace elements of higher masses. The high ⁴He/²¹Ne ratio of 420 in Acuña metal indicates that the samples were at a deep position within a very large meteoroid. The exposure ages of Acuña were estimated to be 50–200 Ma from ³He, ²¹Ne and ³⁸Ar abundances and by utilizing the diagrams of production rates vs. the ⁴He/²¹Ne ratio based on the Signer-Nier model. The low exposure age of Acuña may indicate a history different from that of other IIIAB irons whose exposure ages cluster at ～670 Ma. Otherwise, Acuña may be one of the samples with the low production rate, which can not be estimated from the diagrams of the Signer-Nier model.     

Remnants of altered meteorite in the Cretaceous‐Paleogene clay boundary in Poland

Fossil iron meteorites are extremely rare in the geological sedimentary record. The paleometeorite described here is the first such finding at the Cretaceous‐Paleogene (K‐Pg) boundary. In the boundary clay from the outcrop at the Lechówka quarry (Poland), fragments of the paleometeorite were found in the bottom part of the host layer. The fragments of meteorite (2–6 mm in size) and meteoritic dust are metallic‐gray in color and have a total weight of 1.8181 g. Geochemical and petrographic analyses of the meteorite from Lechówka reveal the presence of Ni‐rich minerals with a total Ni amount of 2–3 wt%. The identified minerals are taenite, kamacite, schreibersite, Ni‐rich magnetite, and Ni‐rich goethite. No relicts of silicates or chromites were found. The investigated paleometeorite apparently represents an independent fall and does not seem to be derived from the K‐Pg impactor. The high degree of weathering did not permit the chemical classification of the meteorite fragments. However, the recognized mineral inventory, lack of silicates, and their pseudomorphs and texture may indicate that the meteorite remains were an iron meteorite.     

Frontier Mountain 93001: A coarse‐grained,enstatite‐augite‐oligoclase‐rich,igneous rock from the acapulcoite‐lodranite parent asteroid

Abstract— The Frontier Mountain (FRO) 93001 meteorite is a 4.86 g fragment of an unshocked, medium‐ to coarse‐grained rock from the acapulcoite‐lodranite (AL) parent body. It consists of anhedral orthoenstatite (Fs_{13.3 ± 0.4}Wo_{3.1 ± 0.2}), augite (Fs_{6.1 ± 0.7}Wo_{42.3 ± 0.9}; Cr₂O₃ = 1.54 ± 0.03), and oligoclase (Ab_{80.5 ± 3.3}Or_{3.1 ± 0.6}) up to >1 cm in size enclosing polycrystalline aggregates of fine‐grained olivine (average grain size: 460 ± 210 μm) showing granoblastic textures, often associated with Fe,Ni metal, troilite, chromite (cr# = 0.91 ± 0.03; fe# = 0.62 ± 0.04), schreibersite, and phosphates. Such aggregates appear to have been corroded by a melt. They are interpreted as lodranitic xenoliths. After the igneous (the term “igneous” is used here strictly to describe rocks or minerals that solidified from molten material) lithology intruding an acapulcoite host in Lewis Cliff (LEW) 86220, FRO 93001 is the second‐known silicate‐rich melt from the AL parent asteroid. Despite some similarities, the silicate igneous component of FRO 93001 (i.e., the pyroxene‐plagioclase mineral assemblage) differs in being coarser‐grained and containing abundant enstatite. Melting‐crystallization modeling suggests that FRO 93001 formed through high‐degree partial melting (≥35 wt%; namely, ≥15 wt% silicate melting and ?20 wt% metal melting) of an acapulcoitic source rock, or its chondritic precursor, at temperatures ≥1200 °C, under reducing conditions. The resulting magnesium‐rich silicate melt then underwent equilibrium crystallization; prior to complete crystallization at ?1040 °C, it incorporated lodranitic xenoliths. FRO 93001 is the highest‐temperature melt from the AL parent‐body so far available in laboratory. The fact that FRO 93001 could form by partial melting and crystallization under equilibrium conditions, coupled with the lack of quench‐textures and evidence for shock deformation in the xenoliths, suggests that FRO 93001 is a magmatic rock produced by endogenic heating rather than impact melting.     

Gebel Kamil: The iron meteorite that formed the Kamil crater (Egypt)

Abstract– The 45 m in diameter Kamil impact crater was formed <5000 yr ago in the eastern Sahara, close to the southern border of modern Egypt. The original features of this structure, including thousands of fragments of the meteorite impactor, are extremely well preserved. With the exception of a single 83 kg regmaglypted individual, all specimens of Gebel Kamil (the iron meteorite that formed the Kamil crater) are explosion fragments weighing from <1 g to 34 kg. Gebel Kamil is an ungrouped Ni‐rich (about 20 wt% Ni) ataxite characterized by high Ge and Ga contents (approximately 120 μg g^?1 and approximately 50 μg g^?1, respectively) and by a very fine‐grained duplex plessite metal matrix. Accessory mineral phases in Gebel Kamil are schreibersite, troilite, daubréelite, and native copper. Meteorite fragments are cross‐cut by curvilinear shear bands formed during the explosive terrestrial impact. A systematic search around the crater revealed that meteorite fragments have a highly asymmetric distribution, with greater concentrations in the southeast sector and a broad maximum in meteorite concentration in the 125–160° N sector at about 200 m from the crater rim. The total mass of shrapnel specimens >10 g, inferred from the density map compiled in this study is 3400 kg. Field data indicate that the iron bolide approached the Earth’s crust from the northwest (305–340° N), travelling along a moderately oblique trajectory. Upon hypervelocity impact, the projectile was disrupted into thousands of fragments. Shattering was accompanied by some melting of the projectile and of the quartz‐arenite target rocks, which also suffered shock metamorphism.