Mineralogy of iron sulfides in CM1 and CI1 lithologies of the Kaidun breccia: Records of extreme to intense hydrothermal alteration

The polymict Kaidun microbreccia contains lithologies of C‐type chondrites with euhedral iron sulfide crystals of hydrothermal origin. Our FIB‐TEM study reveals that acicular sulfides in a CM1 lithology are composed of Fe‐rich pyrrhotite with nonintegral vacancy superstructures (NC‐pyrrhotite), troilite, and pentlandite, all showing distinct exsolution textures. Based on phase relations in the Fe‐Ni‐S system, we constrain the temperature of formation of the originally homogeneous monosulfide solid solution to the range of 100–300 °C. In some crystals the exsolution of pentlandite and the microtextural equilibration was incomplete, probably due to rapid cooling. We use thermodynamic modeling to constrain the physicochemical conditions of the extreme hydrothermal alteration in this lithology. Unless the CM1 lithology was sourced from a large depth in the parent body (internal pressure >85 bar) or the temperatures were in the lower range of the interval determined, the water was likely present as vapor. Previously described light δ³⁴S compositions of sulfides in Kaidun's CM1 lithology are likely due to the loss of ³⁴S‐enriched H₂S during boiling. Platy sulfide crystals in an adjacent, intensely altered CI1 lithology are composed of Fe‐poor, monoclinic 4C‐pyrrhotite and NC‐pyrrhotite and probably formed at lower temperatures and higher fS₂ relative to the CM1 lithology. However, a better understanding of the stability of Fe‐poor pyrrhotites at temperatures below 300 °C is required to better constrain these conditions.     

Organics preserved in anhydrous interplanetary dust particles: Pristine or not?

The chondritic‐porous subset of interplanetary dust particles (CP‐IDPs) are thought to have a cometary origin. Since the CP‐IDPs are anhydrous and unaltered by aqueous processes that are common to chondritic organic matter (OM), they represent the most pristine material of the solar system. However, the study of IDP OM might be hindered by their further alteration by flash heating during atmospheric entry, and we have limited understanding on how short‐term heating influences their organic content. In order to investigate this problem, five CP‐IDPs were studied for their OM contents, distributions, and isotopic compositions at the submicro‐ to nanoscale levels. The OM contained in the IDPs in this study spans the spectrum from primitive OM to that which has been significantly processed by heat. Similarities in the Raman D bands of the meteoritic and IDP OMs indicate that the overall gain in the sizes of crystalline domains in response to heating is similar. However, the Raman Γ_G values of the OM in all of the five IDPs clearly deviate from those of chondritic OM that had been processed during a prolonged episode of parent body heating. Such disparity suggests that the nonaromatic contents of the OM are different. Short duration heating further increases the H/C ratio and reduces the δ¹³C and δD values of the IDP OM. Our findings suggest that IDP OM contains a significant proportion of disordered C with low H content, such as sp² olefinic C=C, sp³ C–C, and/or carbonyl contents as bridging material.     

Heterogeneous histories of Ni‐bearing pyrrhotite and pentlandite grains in the CI chondrites Orgueil and Alais

Compositional and structural analyses of CI chondrite iron–nickel sulfide grains reveal heterogeneity both across and within the Orgueil and Alais meteorites. Orgueil grains with the 4C monoclinic pyrrhotite structure have variable metal‐to‐sulfur ratios and nickel contents. These range from the nominal ratio of 0.875 for Fe₇S₈ with <1 atom% nickel to a high metal‐to‐sulfur ratio of 0.97 with 15 atom% nickel. These data reveal a previously unrecognized low‐temperature solid solution between Fe₇S₈ and Fe₅Ni₃S₈. We have also identified 6C monoclinic pyrrhotite among the Orgueil iron–nickel sulfides. The occurrence of pentlandite in Orgueil is confirmed for the first time crystallographically. In contrast, sulfide grains in Alais do not show the same spread in composition and structure; rather they represent the endmembers: low‐Ni 4C monoclinic pyrrhotite and pentlandite. We investigate possible formation/alteration scenarios: crystallization from a melt, solid‐state diffusion and/or exsolution, oxidation of pre‐existing sulfides, and precipitation from a fluid. Sulfide grains are sensitive to alteration conditions; these data suggest that the structures and compositions of the sulfide assemblages in Orgueil and Alais were established by late‐stage parent body aqueous alteration, followed in some cases by low‐temperature solid‐state processes. The samples record different alteration histories, with Orgueil experiencing lower equilibration temperatures (25 °C) than Alais (100–135 °C). We conclude that millimeter‐scale heterogeneity existed in alteration conditions (e.g., temperature, pH, oxygen fugacity, sulfur fugacity, duration of alteration) on the parent body. This variability is evidenced by the diversity among sulfide grains located within millimeters of one another.     

Infrared spectroscopy of interplanetary dust in the laboratory

Diagnostic infrared spectra of individual nanogram-sized interplanetary dust particles (IDPs) collected in the Earth's stratosphere have been obtained. A mount containing three crushed “chondritic” IDPs shows features near 1000 and 500 cm^?1, suggestive of crystalline pyroxene, and different from those of crystalline olivine, amorphous olivine, or meteoritic clay minerals. The structural diversity of chondritic IDPs and possible effects of atmospheric heating must be considered when comparing this spectrum with astrophysical spectra of interplanetary and cometary dust. Transmission electron microscope (TEM) and infrared observations are also reported on one member of the rare subset of IDPs which resemble hydrated carbonaceous chondrite matrix material. The infrared spectrum of this particle between 4000 and 400 cm^?1 closely matches that of the C2 meteorite Murchison. TEM observations suggest that this class of particles might serve as a thermometer for the process of heating on atmospheric entry.     

A new variant of saponite‐rich micrometeorites recovered from recent Antarctic snowfall

Abstract– Eight saponite‐rich micrometeorites with very similar mineralogy were found from the recent surface snow in Antarctica. They might have come to Earth as a larger meteoroid and broke up into pieces on Earth, because they were recovered from the same layer and the same location of the snow. Synchrotron X‐ray diffraction (XRD) analysis indicates that saponite, Mg‐Fe carbonate, and pyrrhotite are major phases and serpentine, magnetite, and pentlandite are minor phases. Anhydrous silicates are entirely absent from all micrometeorites, suggesting that their parental object has undergone heavy aqueous alteration. Saponite/serpentine ratios are higher than in the Orgueil CI chondrite and are similar to the Tagish Lake carbonaceous chondrite. Transmission electron microscope (TEM) observation indicates that serpentine occupies core regions of fine‐grained saponite, pyrrhotite has a low‐Ni concentration, and Mg‐Fe carbonate shows unique concentric ring structures and has a mean molar Mg/(Mg + Fe) ratio of 0.7. Comparison of the mineralogy to hydrated chondrites and interplanetary dust particles (IDPs) suggests that the micrometeorites are most similar to the carbonate‐poor lithology of the Tagish Lake carbonaceous chondrite and some hydrous IDPs, but they show a carbonate mineralogy dissimilar to any primitive chondritic materials. Therefore, they are a new variant of saponite‐rich micrometeorite extracted from a primitive hydrous asteroid and recently accreted to Antarctica.     

Fe‐Ni metal and sulfide minerals in CM chondrites: An indicator for thermal history

Abstract– CM chondrites were subjected to aqueous alteration and, in some cases, to secondary metamorphic heating. The effects of these processes vary widely, and have mainly been documented in silicate phases. Herein, we report the characteristic features of Fe‐Ni metal and sulfide phases in 13 CM and 2 CM‐related chondrites to explore the thermal history of these chondrites. The texture and compositional distribution of the metal in CM are different from those in unequilibrated ordinary and CO chondrites, but most have similarities to those in highly primitive chondrites, such as CH, CR, and Acfer 094. We classified the CM samples into three categories based on metal composition and sulfide texture. Fe‐Ni metal in category A is kamacite to martensite. Category B is characterized by pyrrhotite grains always containing blebs or lamellae of pentlandite. Opaque mineral assemblages of category C are typically kamacite, Ni‐Co‐rich metal, and pyrrhotite. These categories are closely related to the degree of secondary heating and are not related to degree of the aqueous alteration. The characteristic features of the opaque minerals can be explained by secondary heating processes after aqueous alteration. Category A CM chondrites are unheated, whereas those in category B experienced small degrees of secondary heating. CMs in category C were subjected to the most severe secondary heating process. Thus, opaque minerals can provide constraints on the thermal history for CM chondrites.     

Noble gases in interplanetary dust particles,II: Excess helium‐3 in cluster particles and modeling constraints on interplanetary dust particle exposures to cosmic‐ray irradiation

Abstract— Measurements of He isotopes in cluster interplanetary dust particles (IDPs) from stratospheric dust collector L2009 reveal anomalous ³He/⁴He ratios comparable to those seen earlier, up to ～40x the solar wind ratio, in particles from the companion collector L2011. These overabundances of ³He in the L2009 samples are masked by much higher ⁴He contents compared to the L2011 particles, and are visible only in minor gas fractions evolved by stepwise heating at high temperatures. Cosmic‐ray induced spallogenic reactions are efficient producers of ³He. The majority of this paper is devoted to a detailed assessment of the possible role of spallation in generating the ³He excesses in these and other cluster IDPs. A model of collisional erosion and fragmentation during inward transit through the interplanetary dust environment is used to estimate space lifetimes of particles from asteroidal and Edgeworth–Kuiper Belt sources. Results of the modeling indicate that Poynting–Robertson orbital evolution timescales of IDPs small enough to elude destruction on their way to Earth from either location are far shorter than the cosmic‐ray exposure ages required to account for observed ³He overabundances. Grains large enough to have sufficiently long space residence times are fragmented close to their sources. An alternative to long in‐space exposure could be prolonged irradiation of particles buried in parent body regoliths prior to their ejection as IDPs. A qualitative calculation suggests, however, that collisional erosion of asteroidal upper‐regolith materials is likely to occur on timescales shorter than the > 1 Ga burial times needed for accumulation of spallogenic ³He to the levels seen in several cluster particles. In contrast, regoliths on Edgeworth–Kuiper Belt objects may be stable enough to account for the ³He excesses, and delivery of heavily pre‐irradiated IDPs to the inner solar system by short‐period Edgeworth–Kuiper Belt comets remains a possibility. A potential problem is that the expected associated abundances of spallation‐produced ²¹Ne appear to be absent, although here the present IDP data base is too sparse and for the most part too imprecise to rule out a spallogenic origin. Relatively short periods of pre‐ejection residence in asteroidal regoliths may be responsible for the curiously broad exposure age distributions reported for micrometeorites extracted from Greenland and sea‐floor sediments.     

Survival of organic phases in porous IDPs during atmospheric entry: A pulse‐heating study

Abstract— In this study, we have performed pulse‐heating experiments at different temperatures for three organic molecules (a polycyclic aromatic hydrocarbon [PAH], a ketone, and an amino acid) absorbed into microporous aluminum oxide (Al₂O₃) in order to imitate the heating of the organic molecules in interplanetary dust particles (IDPs) and micrometeorites (MMs) during atmospheric entry and to investigate their survival. We have shown that modest amounts (a few percent) of these organic molecules survive pulse‐heating at temperatures in the 700 to 900 °C range. This suggests that the porosity in IDPs and MMs, combined with a sublimable phase (organic material, water), produces an ablative cooling effect, which permits the survival of organic molecules that would otherwise be lost either by thermal degradation or evaporation during atmospheric entry.     

The smallest comet 81P/Wild 2 dust dances around the CI composition

The bulbous Stardust track #80 (C2092,3,80,0,0) is a huge cavity. Allocations C2092,2,80,46,1 nearest the entry hole and C2092,2,80,47,6 about 0.8 mm beneath the entry hole provide evidence of highly chaotic conditions during capture. They are dominated by nonvesicular low‐Mg silica glass instead of highly vesicular glass found deeper into this track which is consistent with the escape of magnesiosilica vapors generated from the smallest comet grains. The survival of delicate (Mg,Al,Ca)‐bearing silica glass structures is unique to the entry hole. Both allocations show a dearth of surviving comet dust except for a small enstatite, a low‐Ca hypersthene grain, and a Ti‐oxide fragment. Finding scattered TiO₂ fragments in the silica glass could support, but not prove, TiO₂ grain fragmentation during hypervelocity capture. The here reported dearth in mineral species is in marked contrast to the wealth of surviving silicate and oxide minerals deeper into the bulb. Both allocations show Fe‐Ni‐S nanograins dispersed throughout the low‐Mg silica glass matrix. It is noted that neither comet Halley nor Wild 2 had a CI bulk composition for the smallest grains. Using the analogs of interplanetary dust particles (IDPs) and cluster IDPs it is argued that a CI chondritic composition requires the mixing of nonchondritic components in the appropriate proportions. So far, the fine‐grained Wild 2 dust is biased toward nonchondritic ferromagnesiosilica materials and lacking contributions of nonchondritic components with Mg‐Fe‐Ni‐S[Si‐O] compositions. To be specific, “Where are the GEMS”? The GEMS look‐alike found in this study suggests that evidence of GEMS in comet Wild 2 may still be found in the Stardust glass.     

Space radiation processing of sulfides and silicates in primitive solar systems materials: Comparative insights from in situ TEM ion irradiation experiments

Abstract– Mineral grains that comprise dust particles in circumstellar, interstellar, and protostellar environments can potentially undergo amorphization and other solid‐state transformations from exposure to energetic ions from space plasmas. The Fe‐sulfide minerals troilite (FeS) and pyrrhotite (Fe_1?xS) are important known dust components, but their potential to undergo structural changes, including amorphization, from space radiation processing in dusty space environments has not been experimentally evaluated relative to silicates. We used a transmission electron microscope (TEM) with capabilities for in situ ion irradiation to precisely follow structural changes in troilite and pyrrhotite exposed to 1.0 MeV Kr⁺⁺ ions selected to optimize the probability of inducing amorphization from nuclear elastic collisional processes. No indication of amorphization was found in either mineral up to an experimentally practical ion dose of 1 × 10¹⁶ Kr⁺⁺ ions cm^?2, indicating that both structures can remain crystalline up to a modeled collisional damage level of at least 26 displacements‐per‐atom. This behavior matches that of some of the most radiation‐resistant nonmetallic phases known, and is two orders of magnitude higher than the levels at which Mg‐rich olivine and enstatite become amorphous under the same irradiation conditions. Although pyrrhotite retained short‐range crystalline order during irradiation, its longer range vacancy‐ordered superstructure is removed at modeled damage levels equivalent to those at which olivine and enstatite become amorphous. This suggests that space radiation conditions sufficient to amorphize olivine and enstatite in circumstellar and interstellar environments would convert coexisting pyrrhotite to its disordered structural form, thereby changing magnetic and possibly other properties that determine how pyrrhotite will behave in these environments.     

Noble gas space exposure ages of individual interplanetary dust particles

Abstract— The He, Ne, and Ar compositions of 32 individual interplanetary dust particles (IDPs) were measured using low‐blank laser probe gas extraction. These measurements reveal definitive evidence of space exposure. The Ne and Ar isotopic compositions in the IDPs are primarily a mixture between solar wind (SW) and an isotopically heavier component dubbed “fractionated solar” (FS), which could be implantation‐fractionated solar wind or a distinct component of the solar corpuscular radiation previously identified as solar energetic particles (SEP). Space exposure ages based on the Ar content of individual IDPs are estimated for a subset of the grains that appear to have escaped significant volatile losses during atmosphere entry. Although model‐dependent, most of the particles in this subset have ages that are roughly consistent with origin in the asteroid belt. A short (<1000 years) space exposure age is inferred for one particle, which is suggestive of cometary origin. Among the subset of grains that show some evidence for relatively high atmospheric entry heating, two possess elevated ²¹Ne/²²Ne ratios generated by extended exposure to solar and galactic cosmic rays. The inferred cosmic ray exposure ages of these particles exceeds 10⁷ years, which tends to rule out origin in the asteroid belt. A favorable possibility is that these ²¹Ne‐rich IDPs previously resided on a relatively stable regolith of an Edgeworth‐Kuiper belt or Oort cloud body and were introduced into the inner solar system by cometary activity. These results demonstrate the utility of noble gas measurements in constraining models for the origins of interplanetary dust particles.     

Sulfide mineralogy and redox conditions in some shergottites

Abstract— Magmatic sulfide mineralogy has been studied in 2 olivine‐phyric shergottites (DaG 476 and SaU 005) and 4 basaltic shergottites (Zagami, Shergotty, Los Angeles, and NWA 480). Modal abundances of magmatic sulfides, as estimated by image analysis on thin section, are high (0.16 to 0.53 area percent) and correlate positively with abundances of Fe‐Ti oxides. Sulfides are mesostasis minerals, being mostly interstitial grains or locally enclosed in post‐cumulus melt inclusions (e.g., SaU 005) in olivine. Sulfides in shergottites are composed of major pyrrhotite containing pentlandite exsolutions associated with minor amounts of Cu sulfides (chalcopyrite and/or cubanite). Hot desert finds (e.g., DaG 476) show abundant fracture‐filling iron (oxy)hydroxides of probable terrestrial origin. Unaltered sulfides show metal‐rich hexagonal pyrrhotite compositions with metal/sulfur (M/S) ratio ranging between 0.936 ± 0.005 and 0.962 ± 0.01. This compositional range corresponds to the two‐phase structural domain 2C + nC of the Fe‐S system; however, the high‐temperature disordered hexagonal 1C pyrrhotite structure would be in better agreement with magnetic properties of shergottites. Ni contents in pyrrhotite increase from Los Angeles (<0.05 at%) to Shergotty, Zagami, and NWA 480 (0.2–0.5 at%), and DaG 476 and SaU 005 (up to 3 at%). The higher Ni values of pyrrhotite in olivine‐phyric shergottites correlate with the abundance of pentlandite exsolutions, both reflecting more primitive Ni‐rich sulfide liquids where abundant olivine crystallized. This result and the strong correlation between sulfide abundances and Fe‐Ti oxides argue for a primary magmatic origin of these sulfides. Although they reproduce the trend of magmatic oxygen fugacity conditions determined from Fe‐Ti oxide pairs, observed pyrrhotite compositions are systematically more metal‐deficient compared to those calculated from the Fe‐S‐O system. This suggests post‐magmatic oxidation during cooling on Mars, followed by terrestrial weathering for hot desert finds.     

What metal‐troilite textures can tell us about post‐impact metamorphism in chondrite meteorites

Abstract— Metal‐troilite textures are examined in metamorphosed and impact‐affected ordinary chondrites to examine the response of these phases to rapid changes in temperature. Complexly intergrown metal‐troilite textures are shown to form in response to three different impact‐related processes. (1) During impacts, immiscible melt emulsions form in response to spatially focused heating. (2) Immediately after impact events, re‐equilibration of heterogeneously distributed heat promotes metamorphism adjacent to zones of maximum impact heating. Where temperatures exceed ～850 ° C, this post‐impact metamorphism results in melting of conjoined metal‐troilite grains in chondrites that were previously equilibrated through radiogenic metamorphism. When the resulting Fe‐Ni‐S melt domains crystallize, a finely intergrown mixture of troilite and metal forms, which can be zoned with kamacite‐rich margins and taenite‐rich cores. (3) At lower temperatures, post‐impact metamorphism can also cause liberation of sulfur from troilite, which migrates into adjacent Fe‐Ni metal, allowing formation of troilite and occasionally copper within the metal during cooling. Because impact events cause heating within a small volume, post‐impact metamorphism is a short duration event (days to years) compared with radiogenic metamorphism (>10⁶ years). The fast kinetics of metal‐sulfide reactions allows widespread textural changes in conjoined metal‐troilite grains during post‐impact metamorphism, whereas the slow rate of silicate reactions causes these to be either unaffected or only partially annealed, except in the largest impact events. Utilizing this knowledge, information can be gleaned as to whether a given meteorite has suffered a post‐impact thermal overprint, and some constraints can be placed on the temperatures reached and duration of heating.     

The ultrafine mineralogy of a molten interplanetary dust particle as an example of the quench regime of atmospheric entry heating

Abstract— Melting and degassing of interplanetary dust particle L2005B22 at ～1200 °C was due to flash heating during atmospheric entry. Preservation of the porous particle texture supports rapid quenching from the peak heating temperature whereby olivine and pyroxene nanocrystals (3 nm-26 nm) show partial devitrification of the quenched melt at T ? 450 °C–740 °C. The implied ultrahigh cooling rates are calculated at ～105 °C/h–106 °C/h, which is consistent with quench rates inferred from the temperature-time profiles based on atmospheric entry heating models. A vesicular rim on a nonstoichiometric relic forsterite grain in this particle represents either evaporative magnesium loss during flash heating or thermally annealed ion implantation texture.     

Combined noble gas and trace element measurements on individual stratospheric interplanetary dust particles

Abstract— The trace element compositions and noble gas contents of 32 individual interplanetary dust particles (IDPs) collected in the Earth's stratosphere were measured. Trace element compositions are generally similar to CI meteorites, with occasional depletions in Zn/Fe with respect to CI. Noble gases were detected in all but one of the IDPs. Noble gas elemental compositions are consistent with the presence of fractionated solar wind. A rough correlation between surface‐normalized He abundances and Zn/Fe ratios is observed; Zn‐poor particles generally have lower He contents than the other IDPs. This suggests that both elements were lost by frictional heating during atmospheric entry and confirms the view that Zn can serve as an entry‐heating indicator in IDPs.     

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.     

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

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

Sulfide–oxide assemblages in Acfer 094—Clues to nebular metal–gas interactions

The ungrouped carbonaceous chondrite Acfer 094 is among the least altered samples of the early solar system. We have studied concentric sulfide–oxide aggregates from this meteorite by transmission electron microscopy (TEM) and nanoscale secondary ion mass spectrometry (NanoSIMS). The main minerals present are magnetite, pentlandite, and pyrrhotite/troilite. The outer parts of the aggregates include μm-sized olivine and pyroxenes with variable Mg/Fe ratios. One aggregate contains taenite (56.7 wt% Ni) within its central part that is surrounded by pentlandite and magnetite. We conclude that both phases have formed by oxidation and sulfidization of metal and, based on the metal and sulfide Fe/Ni ratio, a (sulfide)-formation temperature of 400–550 °C can be constrained. This temperature is higher than any temperature that could be expected to have occurred on the Acfer 094 parent body, and also textural evidence indicates that the aggregates formed before parent-body accretion. We therefore conclude that the formation of the sulfide–oxide aggregates occurred most likely in the solar nebular at highly variable H₂O and H₂S fugacities. Oxygen-isotopic compositions of magnetite within these assemblages show that they are indistinguishable from the meteorite's matrix (δ¹⁷O_SMOW ≈ 4 ± 8‰, δ¹⁸O_SMOW ≈ 10 ± 6‰, and ∆¹⁷O_SMOW ≈ −1 ± 5‰). An enrichment of ^17,18O relative to chondrules of Acfer 094 suggests a link between the formation of the sulfide–oxide aggregates and the preaccretionary processing of matrix grains in a volatile-enriched nebular environment.     

Investigation of iron sulfide impact crater residues: A combined analysis by scanning and transmission electron microscopy

Abstract– Samples returned from comet 81P/Wild 2 by the Stardust mission provided an unequaled opportunity to compare previously available extraterrestrial samples against those from a known comet. Iron sulfides are a major constituent of cometary grains commonly identified within cometary interplanetary dust particles (IDPs) and Wild 2 samples. Chemical analyses indicate Wild 2 sulfides are fundamentally different from those in IDPs. However, as Wild 2 dust was collected via impact into capture media at approximately 6.1 km s^?1, it is unclear whether this is due to variation in preaccretional/parent body processes experienced by these materials or due to heating and alteration during collection. We investigated alteration in pyrrhotite and pentlandite impacted into Stardust flight spare Al foils under encounter conditions by comparing scanning and transmission electron microscope (SEM, TEM) analyses of preimpact and postimpact samples and calculating estimates of various impact parameters. SEM is the primary method of analysis during initial in situ examination of Stardust foils, and therefore, we also sought to evaluate the data obtained by SEM using insights provided by TEM. We find iron sulfides experience heating, melting, separation, and loss of S, and mixing with molten Al. These results are consistent with estimated peak pressures and temperatures experienced (approximately 85 GPa, approximately 2600 K) and relative melting temperatures. Unambiguous identification of preserved iron sulfides may be possible by TEM through the location of Al‐free regions. In most cases, the Ni:Fe ratio is preserved in both SEM and TEM analyses and may therefore also be used to predict original chemistry and estimate mineralogy.     

A NanoSIMS and Raman spectroscopic comparison of interplanetary dust particles from comet Grigg‐Skjellerup and non‐Grigg Skjellerup collections

Abstract– Interplanetary dust particles (IDPs) are the most primitive extraterrestrial material available for laboratory studies and may, being likely of cometary origin, sample or represent the unaltered starting material of the solar system. Here we compare IDPs from a “targeted” collection, acquired when the Earth passed through the dust stream of comet 26P/Grigg‐Skjellerup (GSC), with IDPs from nontargeted collections (i.e., of nonspecific origin). We examine both sets to further our understanding of abundances and character of their isotopically anomalous phases to constrain the nature of their parent bodies. We identified ten presolar silicates, two oxides, one SiC, and three isotopically anomalous C‐rich grains. One of seven non‐GSC IDPs contains a wealth of unaltered nebula material, including two presolar silicates, one oxide, and one SiC, as well as numerous δD and δ¹⁵N hotspots, demonstrating its very pristine character and suggesting a cometary origin. One of these presolar silicates is the most ¹⁷O‐rich discovered in an IDP and has been identified as a possible GEMS (glass with embedded metal and sulfides). Organic matter in an anhydrous GSC IDP is extremely disordered and, based on Raman spectral analyses, appears to be the most primitive IDP analyzed in this study, albeit only one presolar silicate was identified. No defining difference was seen between the GSC and non‐GSC IDPs studied here. However, the GSC collectors are expected to contain IDPs of nonspecific origin. One measure alone, such as presolar grain abundances, isotopic anomalies, or Raman spectroscopy cannot distinguish targeted cometary from unspecified IDPs, and therefore combined studies are required. Whilst targeted IDP populations as a whole may not show distinguishable parameters from unspecified populations (due to statistics, heterogeneity, sampling bias, mixing from other cometary sources), particular IDPs in a targeted collection may well indicate special properties and a fresh origin from a known source.