Fractionation of refractory siderophile elements in metal from the Rose City meteorite

Abstract— An ～4 × 9 × 12-mm concentration of metal (dubbed RC1) situated between silicate melt and a relict chondritic clast in the Rose City H5 impact-melt breccia is compositionally heterogeneous. Approximately 65 wt% of RC1 is enriched in the refractory siderophile elements, Os and Ir, by 30–40% relative to bulk H chondrite metal; ～20 wt% is depleted in these elements by 31–35%; and 15 wt% is depleted by a considerably greater amount (75%). Common and volatile siderophile elements are essentially unfractionated in all three regions; W is fractionated to only a moderate degree. The compositions of the different regions of RC1 are similar to those of previously analyzed metal nodules and veins in shocked but unmelted ordinary chondrites. All of these objects probably formed by a complex process involving vaporization of chondritic material, rapidly followed by oxidation of W to form volatile oxides, fractional condensation of refractory siderophile elements, transport of the residual vapor (containing common and volatile siderophile elements as well as W oxide) and condensation of this vapor in fractures and voids or on metallic liquid substrates. The common occurrence of vugs in shock-heated chondrites and the pervasiveness of vaporization effects recorded in metal masses and veins underscores the important role of superheating in the formation of impact breccias.     

Are high‐temperature fractionations in the solar nebula preserved in highly siderophile element systematics of the Earth's mantle?

Abstract— The relative abundances of the highly siderophile elements (HSE) Os, Ir, Ru, Pt, Rh, and Pd in relatively pristine lherzolites differ from solar abundance ratios and are several orders of magnitude higher than predicted for equilibrium distribution between metal/silicate (core‐mantle). The samples are characterized by a mean Ca/Al ratio of 1.18 ± 0.09 σ_M and a mean Ca/Si ratio of 0.10 ± 0.01 σ_M, overlapping with a mean Ca/Al of 1.069 ± 0.044 σ_M and a mean Ca/Si of 0.081 ± 0.023 σ_M found in chondrites (Wasson and Kallemeyn 1988). Interestingly, the CI‐normalized abundance pattern shows decreasing solar system normalized abundances with increasing condensation temperatures. The abundance of the moderately volatile element Pd is about 2x higher than those in the most refractory siderophiles Ir and Os. Thus, the HSE systematics of upper mantle samples suggest that the late bombardment, which added these elements to the accreting Earth, more closely resembles materials of highly reduced EH or EL chondrites than carbonaceous chondrites. In fact, the HSE in the Earth mantle are even more fractionated than the enstatite chondrites—an indication that some inner solar system materials were more highly fractionated than the latter.     

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.     

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.     

Roosevelt County 075: A petrologic,chemical and isotopic study of the most unequilibrated known H chondrite

Abstract— Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite, δ¹³C). Petrologic subtype 3.2± 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most unequilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.     

Highly siderophile element and 187Re‐187Os isotopic systematics of ungrouped achondrite Northwest Africa 7325: Evidence for complex planetary processes

The abundances of highly siderophile elements (HSE; including Re, Os, Ir, Ru, Pt, and Pd) and ¹⁸⁷Re‐¹⁸⁷Os isotopic systematics were determined for two fragments from ungrouped achondrite NWA 7325. Rhenium‐Os systematics are consistent with closed‐system behavior since formation or soon after. The abundances of the HSE were therefore largely unaffected by late‐stage secondary processes such as shock or terrestrial weathering. As an olivine gabbro cumulate, this meteorite has a bulk composition consistent with derivation from a body that produced a core, mantle, and crust. Also consistent with derivation from a body that produced a core, both fragments of NWA 7325 have HSE abundances that are highly depleted compared to bulk chondrites. One fragment has ~0.002× CI chondrite Ir and relative HSE abundances similar to bulk chondrites. The other fragment has ~0.0002× CI chondrite Ir and relative HSE abundances that are fractionated compared to bulk chondrites. The chondritic relative HSE abundances of the fragment characterized by higher HSE abundances most likely reflect the addition of exogenous chondritic material during or after crystallization by surface impacts. The HSE in the other fragment is likely more representative of the parent body crust. One formation model that can broadly account for the HSE abundances in this fragment is multiple episodes of low‐pressure metal‐silicate equilibration, followed by limited late accretion and mantle homogenization. Given the different HSE compositions of the two adjoining fragments, this meteorite provides an example of the overprint of global processes (differentiation and late accretion) by localized impact contamination.     

Clues to the nature of the impacting bodies from platinum-group elements (rhenium and gold) in borehole samples from the Clearwater East crater (Canada) and the Boltysh impact crater (Ukraine)

Abstract— Seven large (10 g) impact melt rock samples from boreholes from the Boltysh impact crater (Ukraine) and six samples from the East Clearwater crater (Canada) were analyzed for Os, Ir, Ru, Rh, Pd, Re and Au by the nickel sulfide technique in combination with neutron activation. Earlier analyses of Clearwater East impact melt rocks have shown that they are strongly enriched in Ir, Os, Pd and Re. In this work, I confirm earlier findings and demonstrate similarly high enrichments of Rh and Ru. The average Os/Ir, Ru/Ir, Pd/Ir, Rh/Ir and Ru/Rh ratios of the melt rock samples from Clearwater East are CI-chondritic and yield an average Ir content of 25.2 ± 6.5 ng/g relative to an average upper crust concentration of 0.03 ± 0.02 ng/g Ir. The amount of meteoritic component corresponds to 4 to 7% of a nominal CI component for Clearwater East. The impact melt rock samples from a bore hole from Boltysh are low in Ir with an average of 0.2 ± 0.1 ng/g. The CI-normalized abundances increase from the refractory to the more volatile siderophile elements (Os < Ir < Ru < Rh ～ Pd ～ Au ～ Ni ～ Co). Because of the low Ir anomaly and uncertainties in making corrections (correlations are weak) for indigenous siderophile elements, no clear projectile assignment can be made.     

Radiogenic isotope investigation of the St‐Robert H5 fall

Abstract— The St‐Robert H5 chondrite yields a mineral/whole‐rock Pb‐Pb age of 4565 ± 23 Ma (2σ) comparable to the accepted age of most chondrites. The regression of chondrule data give a similar age of 4566 ± 7 Ma (2σ). These results imply that no major perturbation affected the Pb‐Pb systematics of this meteorite's parent body within the first few billion years following its accretion. Re and Os concentrations along with Os isotopic compositions of whole‐rock fragments, surface fusion crusts and metal phases are also reported. The whole rock measurements for this ordinary chondrite are characterized by high Re/Os ratio coupled with relatively high ¹⁸⁷Os/¹⁸⁸Os (compared to average ordinary chondrites), that we interpret as a long term Re enrichment. As for most chondrites, no precise geochronological information could be extracted from the Re/Os systematics, although most data plot near the IIIAB reference isochron (Smoliar et al. 1996). From the fusion crust results, we rule out the possibility that atmospheric entry caused the perturbations in the Re‐Os system, since melted crust analysis yields among the most concordant data points. Evidence from metal phases suggests that a very recent process perturbed the isochron, relocating Re from kamacite toward troilite.     

Re-Os isotope systematics and fractionation of siderophile elements in metal phases from CBa chondrites

We report Os isotope compositions of metal grains in two CB_a chondrites (Bencubbin and Gujba) determined using a micromilling sampling coupled with thermal ionization mass spectrometry, together with the abundances of major and trace siderophile elements obtained by electron probe microanalysis and femtosecond laser ablation inductively coupled plasma–mass spectrometry. The CB_a metal grains presented ¹⁸⁷Os/¹⁸⁸Os ratios akin to carbonaceous chondrites with limited variations (0.1257–0.1270). Most of the CB_a metal grains were scattered along a ¹⁸⁷Re-¹⁸⁷Os reference isochron of IIIAB iron meteorites, indicating that the CB_a metals experienced limited Re-Os fractionation at the time of their formation. The Re/Os ratios of sampling spots for the CB_a metals, recast from the observed ¹⁸⁷Os/¹⁸⁸Os ratios, had a positive correlation with their Os/Ir ratios. In addition, the metal grains showed a positive correlation in a Pd/Fe versus Ni/Fe diagram. These correlations suggest that the CB_a metal grains have formed via equilibrium condensation or evaporation from a gaseous reservoir at ~10⁻⁴ bar with enhanced metal abundances. Compared to the Bencubbin metals, the Gujba metals are characterized by having systematically lower Pd/Fe and Ni/Fe ratios that span subchondritic values. Such a difference was most likely induced by the compositionally heterogeneous impact plume from which the metals were condensed.     

Origin and age of metal veins in Canyon Diablo graphite nodules

Previous studies attributed the origin of metal veins penetrating graphite nodules in the Canyon Diablo IAB main group iron meteorite to condensation from vapor or melting of host metal. Abundances of 16 siderophile elements measured in kamacite within vein and host meteorite are most consistent with an origin by melting of the host metal followed by fractional crystallization of the liquid. The presence of the veins within graphite nodules may be explained by impact, as peak shock temperatures, and thus the most likely areas to undergo metal melting are at metal–graphite interfaces. The origin of the veins is constrained by Re‐Os chronometry to have occurred early (>4 Ga) in solar system history.     

Highly siderophile element and osmium isotope evidence for postcore formation magmatic and impact processes on the aubrite parent body

Abstract– Aubrites exhibit a wide range of highly siderophile element (HSE—Re, Os, Ir, Ru, Rh, Pt, Pd, Au) concentrations and ¹⁸⁷Os/¹⁸⁸Os compositions. Their HSE concentrations are one to three orders of magnitude less than chondrites, with the exception of the Shallowater and Mt. Egerton samples. While most aubrites show chondritic HSE abundance ratios, significant enrichments of Pd and Re relative to Os, Ir, and Ru are observed in 12 of 16 samples. Present‐day ¹⁸⁷Os/¹⁸⁸Os ratios range from subchondritic values of 0.1174 to superchondritic values of up to 0.2263. Half of the samples have ¹⁸⁷Os/¹⁸⁸Os ratios of 0.127 to 0.130, which is in the range of enstatite chondrites. Along with the brecciated nature of aubrites, the HSE and Re‐Os isotope systematics support a history of extensive postaccretion processing, including core formation, late addition of chondritic material and/or core material and potential breakup and reassembly. Highly siderophile element signatures for some aubrites are consistent with a mixing of HSE‐rich chondritic fragments with a HSE‐free aubrite matrix. The enrichments in incompatible HSE such as Pd and Re observed in some aubrites, reminiscent of terrestrial basalts, suggest an extensive magmatic and impact history, which is supported by both the ¹⁸⁷Re‐¹⁸⁷Os isotope system and silicate‐hosted isotope systems (Rb‐Sr, K‐Ar) yielding young formation ages of 1.3–3.9 Ga for a subset of samples. Compared with other differentiated achondrites derived from small planetary bodies, aubrites show a wide range in HSE concentrations and ¹⁸⁷Os/¹⁸⁸Os, most similar to angrites. While similarities exist between the diverse groups of achondrites formed early in solar system history, the aubrite parent body(ies) clearly underwent a distinct evolution, different from angrites, brachinites, ureilites, howardites, eucrites, and diogenites.     

Origin of EL3 chondrites: Evidence for variable C/O ratios during their course of formation—A state of the art scrutiny

Mineral inventories of enstatite chondrites; (EH and EL) are strictly dictated by combined parameters mainly very low dual oxygen (fO₂) and sulfur (fS₂) fugacities. They are best preserved in the Almahata Sitta MS‐17, MS‐177 fragments, and the ALHA 77295 and MAC 88136 Antarctic meteorites. These conditions induce a stark change of the geochemical behavior of nominally lithophile elements to chalcophile or even siderophile and changes in the elemental partitioning thus leading to formation of unusual mineral assemblages with high abundance of exotic sulfide species and enrichment in the metallic alloys, for example, silicides and phosphides. Origin and mode of formation of these exotic chondrites, and their parental source regions could be best scrutinized by multitask research experiments of the most primitive members covering mineralogical, petrological, cosmochemical, and indispensably short‐lived isotopic chronology. The magnitude of temperature and pressure prevailed during their formation in their source regions could eventually be reasonably estimated: pre‐ and postaccretionary could eventually be deduced. The dual low fugacities are regulated by the carbon to oxygen ratios estimated to be >0.83 and <1.03. These parameters not only induce unusual geochemical behavior of the elements inverting many nominally lithophile elements to chalcophile or even siderophile or anthracophile. Structure and mineral inventories in EL3 and EH3 chondrites are fundamentally different. Yet EH3 and EL3 members store crucial information relevant to eventual source regions and importantly possible variation in C/O ratio in the course of their evolution. EL3 and EH3 chondrites contain trichotomous lithologies (1) chondrules and their fragments, (2) polygonal enstatite‐dominated objects, and (3) multiphase metal‐rich nodules. Mineralogical and cosmochemical inventories of lithologies in the same EL3 indicate not only similarities (REE inventory and anomalies in oldhamite) but also distinct differences (sinoite‐enstatite‐graphite relationship). Oldhamite in chondrules and polygonal fragments in EL3 depict negative Eu anomaly attesting a common cosmochemical source. Metal‐dominated nodules in both EL3 and EH3 are conglomerates of metal clasts and sulfide fragments in EH3 and concentrically zoned C‐bearing metal micropebbles (≥25 μm ≤50 μm) in EL3 thus manifesting a frozen in unique primordial accretionary metal texture and composition. Sinoite‐enstatite‐diopside‐graphite textures reveal a nucleation and growth strongly suggestive of fluctuating C/O ratio during their nucleation and growth in the source regions. Mineral inventories, sulfide phase relations, sinoite‐enstatite‐graphite intergrowth, carbon and nitrogen isotopic compositions of graphite, spatial nitrogen abundance in graphite in metal nodules, and last but not least ¹²⁹I/¹²⁹Xe and ⁵³Mn/⁵³Cr systematics negate any previously suggested melting episode, pre‐accretionary or dynamic, in parental asteroids.     

Secondary‐volatiles linked metallic iron in eucrites: The dual‐origin metals of Camel Donga

The unique occurrence of abundant (~1 vol%) near‐pure‐Fe metal in the Camel Donga eucrite is more complicated than previously believed. In addition to that component of groundmass metal, scattered within the meteorite are discrete nodules of much higher kamacite abundance. We have studied the petrology and composition of two of these nodules in the form of samples we call CD2 and CD3. The nodules are ovoids 11 (CD2) to 15 (CD3) mm across, with metal, or inferred preweathering metal, abundances of 12–17 vol% (CD2 is unfortunately quite weathered). The CD3 nodule also includes at its center a 5 mm ovoid clumping (6 vol%) of F‐apatite. Both nodules are fine‐grained, so the high Fe metal and apatite contents are clearly not flukes of inadequate sampling. The metals within the nodules are distinctly Ni‐rich (0.3–0.6 wt%) compared to the pure‐Fe (Ni generally 0.01 wt%) groundmass metals. Bulk analyses of three pieces of the CD2 nodule show that trace siderophile elements Ir, Os, and Co are commensurately enriched; Au is enriched to a lesser degree. The siderophile evidence shows the nodules did not form by in situ reduction of pyroxene FeO. Moreover, the nodules do not show features such as silica‐phase enrichment or pyroxene with reduced FeO (as constrained by FeO/MgO and especially FeO/MnO) predicted by the in situ reduction model. The oxide minerals, even in groundmass samples well away from the nodules, also show little evidence of reduction. Although the nodule boundaries are generally sharp, groundmass‐metal Ni content is anti‐correlated with distance from the CD3 nodule. We infer that the nodules represent materials that originated within impactors into the Camel Donga portion of the eucrite crust, but probably were profoundly altered during later metamorphism/metasomatism. Origin of the pure‐Fe groundmass metal remains enigmatic. In situ reduction probably played an important role, and association in the same meteorite of the Fe‐nodules is probably significant. But the fluid during alteration was probably not (as previously modeled) purely S and O, of simple heat‐driven internal derivation. We conjecture a two‐stage metasomatism, as fluids passed through Camel Donga after impact heating of volatile‐rich chondritic masses (survivors of gentle accretionary impacts) within the nearby crust. First, reduction to form troilite may have been triggered by fluids rich in S₂ and CO (derived from the protonodules?), and then in a distinct later stage, fluids were (comparatively) H₂O‐rich, and thus reacted with troilite to form pure‐Fe metal along with H₂S and SO₂. The early eucrite crust was in places a dynamic fluid‐bearing environment that hosted complex chemical processes, including some that engendered significant diversity among metal+sulfide alterations.     

Rapid effects of terrestrial alteration on highly siderophile elements in the Sutter's Mill meteorite

The ¹⁸⁷Re-¹⁸⁷Os isotopic systematics of many bulk chondrites plot well beyond analytical uncertainties of a primordial isochron. Limited variations in ¹⁸⁷Os/¹⁸⁸Os, coupled with large variations in Re/Os ratios among chondrites, suggest that this apparently open-system behavior is a result of the comparatively recent gain or loss of Re and/or Os. In order to assess whether or not rapid alteration in the terrestrial environment could be responsible for open-system behavior in chondrites, four pieces of the Sutter's Mill meteorite were examined for Os isotopic systematics and abundances of highly siderophile elements. Pieces SM1 and SM2 were collected prior to a rain event, within 2 days of the fall. Pieces SM51 and SM53 were collected after a rain event. There are significant but minor relative and absolute variations in the abundances of the highly siderophile elements, as well as ¹⁸⁷Os/¹⁸⁸Os among the four pieces. Rhenium-Os isotopic data for SM1 and SM2 plot within analytical uncertainties of a primordial isochron, while powders made from SM51 and SM53 do not. These results suggest that interactions with rain caused some redistribution of Re, and to a lesser extent Os, within small pieces of the meteorite. Thus, Re-Os isotopic systematics of <dm-size pieces of chondrites must be considered susceptible to modification after only a short time on the surface, where exposed to rain.     

Ordinary chondrite metallography: Part 2. Formation of zoned and unzoned metal particles in relatively unshocked H,L, and LL chondrites

Abstract— We studied the metallography of Fe‐Ni metal particles in 17 relatively unshocked ordinary chondrites and interpreted their microstructures using the results of P‐free, Fe‐Ni alloy cooling experiments (described in Reisener and Goldstein 2003). Two types of Fe‐Ni metal particles were observed in the chondrites: zoned taenite + kamacite particles and zoneless plessite particles, which lack systematic Ni zoning and consist of tetrataenite in a kamacite matrix. Both types of metal particles formed during metamorphism in a parent body from homogeneous, P‐poor taenite grains. The phase transformations during cooling from peak metamorphic temperatures were controlled by the presence or absence of grain boundaries in the taenite particles. Polycrystalline taenite particles transformed to zoned taenite + kamacite particles by kamacite nucleation at taenite/taenite grain boundaries during cooling. Monocrystalline taenite particles transformed to zoneless plessite particles by martensite formation and subsequent martensite decomposition to tetrataenite and kamacite during the same cooling process. The varying proportions of zoned taenite + kamacite particles and zoneless plessite particles in types 4–6 ordinary chondrites can be attributed to the conversion of polycrystalline taenite to monocrystalline taenite during metamorphism. Type 4 chondrites have no zoneless plessite particles because metamorphism was not intense enough to form monocrystalline taenite particles. Type 6 chondrites have larger and more abundant zoneless plessite particles than type 5 chondrites because intense metamorphism in type 6 chondrites generated more monocrystalline taenite particles. The distribution of zoneless plessite particles in ordinary chondrites is entirely consistent with our understanding of Fe‐Ni alloy phase transformations during cooling. The distribution cannot be explained by hot accretion‐autometamorphism, post‐metamorphic brecciation, or shock processing.     

Siderophile elements in Earth's upper mantle and lunar breccias: Data synthesis suggests manifestations of the same late influx

Abstract— The platinum group elements (PGE; Ru, Rh, Pd, Os, Ir, Pt), Re and Au comprise the highly siderophile elements (HSE). We reexamine selected isotopic and abundance data sets for HSE in upper mantle peridotites to resolve a longstanding dichotomy. Re‐Os and Pt‐Os isotope systematics, and approximately chondritic proportions of PGE in these rocks, suggest the presence in undepleted mantle of a chondrite‐like component, which is parsimoniously explained by late influx of large planetisimals after formation of the Earth's core and the Moon. But some suites of xenolithic and orogenic spinel lherzolites, and abyssal peridotites, have a CI‐normalized PGE pattern with enhanced Pd that is sometimes termed “non‐chondritic”. We find that this observation is consistent with other evidence of a late influx of material more closely resembling enstatite, rather than ordinary or carbonaceous, chondrites. Regional variations in HSE patterns may be a consequence of a late influx of very large objects of variable composition. Studies of many ancient (>3.8 Ga) lunar breccias show regional variations in Au/Ir and suggest that “graininess” existed during the early bombardment of the Earth and Moon. Reliable Pd values are available only for Apollo 17 breccias 73215 and 73255, however. Differences in HSE patterns between the aphanitic and anorthositic lithologies in these breccias show fractionation between a refractory group (Re, Os and Ir) and a normal (Pd, Ni, and Au) group and may reflect the compositions of the impacting bodies. Similar fractionation is apparent between the EH and EL chondrites, whose PGE patterns resemble those of the aphanitic and anorthositic lithologies, respectively. The striking resemblance of HSE and chalcogen (S, Se) patterns in the Apollo aphanites and high‐Pd terrestrial peridotites suggest that the “non‐chondritic” abundance ratios in the latter may be reflected in the composition of planetisimals striking the Moon in the first 700 Ma of Earth–Moon history. Most notably, high Pd may be part of a general enhancement of HSE more volatile than Fe suggesting that the Au abundance in at least parts of the upper mantle may be 1.5 to 2x higher than previously estimated. The early lunar influx may be estimated from observed basin‐sized craters. Comparison of relative influx to Earth and Moon suggests that the enrichment of HSE is limited to the upper mantle above 670 km. To infer enrichment of the whole mantle would require several large lunar impacts not yet identified.     

A database of chondrite analyses including platinum group elements,Ni, Co,Au, and Cr: Implications for the identification of chondritic projectiles

Abstract— Siderophile elements have been used to constrain projectile compositions in terrestrial and lunar impact melt rocks. To obtain a better knowledge of compositional differences between potential chondritic projectile types, meteorite analyses of the elements Ru, Rh, Pd, Os, Ir, Pt, Cr, Co, Ni, and Au were gathered into a database. The presented compilation comprises 806 analyses of 278 chondrites including new ICP‐MS analyses of Allende and two ordinary chondrites. Each data set was evaluated by comparing element ratios of meteorites from the same chondrite group. Characteristic element abundances and ratios were determined for each group. Features observed in the element abundance patterns can be linked directly to the presence of certain components, such as the abundance of refractory elements Os, Ir, and Ru correlating with the occurrence of refractory inclusions in CV, CO, CK, and CM chondrites. The refined characteristic element ratios appear to be representative not only for meteorites, but also for related asteroidal bodies. Chondrite element ratios were compared to previously published values from impact melt rocks of the Popigai and Morokweng impact structures confirming that an identification of the specific type of projectile (L and LL chondrite, respectively) is possible. The assessment for Morokweng is supported by the recent discovery of an LL chondrite fragment in the impact melt rocks. Ultimately, the database provides valuable information for understanding processes in the solar nebula as they are recorded in chondrites. A new type of complementarity between element patterns of CK and EH chondrites is suggested to be the result of condensation, redox, and transportation processes in the solar nebula.     

Impact processing of chondritic planetesimals: Siderophile and volatile element fractionation in the Chico L chondrite

Abstract— A large impact event 500 Ma ago shocked and melted portions of the L‐chondrite parent body. Chico is an impact melt breccia produced by this event. Sawn surfaces of this 105 kg meteorite reveal a dike of fine‐grained, clast‐poor impact melt cutting shocked host chondrite. Coarse (1–2 cm diameter) globules of FeNi metal + sulfide are concentrated along the axis of the dike from metal‐poor regions toward the margins. Refractory lithophile element abundance patterns in the melt rock are parallel to average L chondrites, demonstrating near‐total fusion of the L‐chondrite target by the impact and negligible crystal‐liquid fractionation during emplacement and cooling of the dike. Significant geochemical effects of the impact melting event include fractionation of siderophile and chalcophile elements with increasing metal‐silicate heterogeneity, and mobilization of moderately to highly volatile elements. Siderophile and chalcophile elements ratios such as Ni/Co, Cu/Ga, and Ir/Au vary systematically with decreasing metal content of the melt. Surprisingly small (?10²) effective metal/silicate‐melt distribution coefficients for highly siderophile elements probably reflect inefficient segregation of metal despite the large degrees of melting. Moderately volatile lithophile elements such K and Rb were mobilized and heterogeneously distributed in the L‐chondrite impact breccias whereas highly volatile elements such as Cs and Pb were profoundly depleted in the region of the parent body sampled by Chico. Volatile element variations in Chico and other L chondrites are more consistent with a mechanism related to impact heating rather than condensation from a solar nebula. Impact processing can significantly alter the primary distributions of siderophile and volatile elements in chondritic planetesimals.     

Opaque assemblages in CR2 Graves Nunataks (GRA) 06100 as indicators of shock‐driven hydrothermal alteration in the CR chondrite parent body

We have studied the petrologic characteristics of sulfide‐metal lodes, polymineralic Fe‐Ni nodules, and opaque assemblages in the CR2 chondrite Graves Nunataks (GRA) 06100, one of the most altered CR chondrites. Unlike low petrologic type CR chondrites, alteration of metal appears to have played a central role in the formation of secondary minerals in GRA 06100. Differences in the mineralogy and chemical compositions of materials in GRA 06100 suggest that it experienced higher temperatures than other CR2 chondrites. Mineralogic features indicative of high temperature include: (1) exsolution of Ni‐poor and Ni‐rich metal from nebular kamacite; (2) formation of sulfides, oxides, and phosphates; (3) changes in the Co/Ni ratios; and (4) carbidization of Fe‐Ni metal. The conspicuous absence of pentlandite may indicate that peak temperatures exceeded 600 °C. Opaques appear to have been affected by the action of aqueous fluids that resulted in the formation of abundant oxides, Fe‐rich carbonates, including endmember ankerite, and the sulfide‐silicate‐phosphate scorzalite. We suggest that these materials formed via impact‐driven metamorphism. Mineralogic features indicative of impact metamorphism include (1) the presence of sulfide‐metal lodes; (2) the abundance of polymineralic opaque assemblages with mosaic‐like textures; and (3) the presence of suessite. Initial shock metamorphism probably resulted in replacement of nebular Fe‐Ni metal in chondrules and in matrix by Ni‐rich, Co‐rich Fe metal, Al‐Ti‐Cr‐rich alloys, and Fe sulfides, while subsequent hydrothermal alteration produced accessory oxides, phosphates, and Fe carbonates. An extensive network of sulfide‐metal veins permitted effective exchange of siderophile elements from pre‐existing metal nodules with adjacent chondrules and matrix, resulting in unusually high Fe contents in these objects.     

Parent body histories recorded in Rumuruti chondrite sulfides: Implications for the onset of oxidized,sulfur-rich core formation

Models of planetary core formation beginning with melting of Fe,Ni metal and troilite are not readily applicable to oxidized and sulfur-rich chondrites containing only trace quantities of metal. Cores formed in these bodies must be dominated by sulfides. Siderophile trace elements used to model metallic core formation could be used to model oxidized, sulfide-dominated core formation and identify related meteorites if their trace element systematics can be quantified. Insufficient information exists regarding the behavior of these core-forming elements among sulfides during metamorphism prior to anatexis. Major, minor, and trace element concentrations of sulfides are reported in this study for petrologic type 3–6 R chondrite materials. Sulfide-dominated core-forming components in such oxidized chondrites (ƒO₂ ≥ iron-wüstite) follow metamorphic evolutionary pathways that are distinct from reduced, metal-bearing counterparts. Most siderophile trace elements partition into pentlandite at approximately 10× chondritic abundances, but Pt, W, Mo, Ga, and Ge are depleted by 1–2 orders of magnitude relative to siderophile elements with similar volatilities. The distribution of siderophile elements is further altered during hydrothermal alteration as pyrrhotite oxidizes to form magnetite. Oxidized, sulfide-dominated core formation differs from metallic core formation models both physically and geochemically. Incongruent melting of pentlandite at 865°C generates melts capable of migrating along solid silicate grains, which can segregate to form a Ni,S-rich core at lower temperatures compared to reduced differentiated parent bodies and with distinct siderophile interelement proportions.