The phosphates of IIIAB iron meteorites

Abstract— Thirteen phosphate minerals are found in IIIAB iron meteorites. Four of these (sarcopside, graftonite, johnsomervilleite, and galileiite) constitute the majority of occurrences. The IIIB iron meteorites are confined to occurrences of only these four phosphates. The IIIA iron meteorites may contain one or more of these four phases; they may also contain other rarer phosphates, and silica (in two instances) and a silicate rock (in one instance). Thus, the IIIA lithophile chemistry is more varied than that of the IIIB meteorites. Based on petrographic relations, sarcopside appears to be the first phosphate to form. Graftonite is probably formed by recrystallization of sarcopside. Johnsomervilleite and galileiite exsolved as enclaves in sarcopside or graftonite at lower temperatures, although some of these also nucleated as separate crystals. The IIIAB phosphates are carriers of a group of incompatible lithophile elements: Fe, Mn, Na, Ca, and K, and, rarely, Mg as well as Pb. These elements (and O) were concentrated in a residual, S-rich liquid during igneous fractional crystallization of the IIIAB core mass. The phosphates formed by oxidation of P as the core solidified and excluded O, which increased its partial pressure in the residual liquid. The trace siderophile trends in bulk IIIAB metal are paralleled by a mineralogical trend of the phosphate minerals that formed. For IIIAB meteorites with low-Ir contents in the metal, the phosphates are mainly Fe-Mn phases; at intermediate Ir values, more Na-bearing phosphates appear; at the highest Ir values, the rarer Na-, K-, Mg-, Cr-, and Pb-bearing phosphates appear. The absence of significant amounts of Mg, Si, Al, and Ti suggest depletion of these elements in the core by the overlying mantle.     

Mn‐Cr isotope systematics of the D'Orbigny angrite

Abstract— We have conducted a detailed study of the Mn‐Cr systematics of the angrite D'Orbigny. Here, we report Cr isotopic abundances and Mn/Cr ratios in olivine, pyroxene, glass, chromite, and bulk rock samples from D'Orbigny. ⁵³Cr excesses in these samples correlate well with their respective Mn/Cr ratios and define an isochron with a slope that corresponds to an initial ⁵³Mn/⁵⁵Mn ratio = (3.24 ± 0.04) × 10^?6 and initial ⁵³Cr/⁵²Cr ratio of ?(53) = 0.30 ± 0.03 at the time of isotopic closure. The ⁵³Mn/⁵⁵Mn ratio of the D'Orbigny bulk rock is more than two‐fold the ⁵³Mn/⁵⁵Mn ratio of the angrites Lewis Cliff 86010 (LEW) and Angra dos Reis (ADOR) and implies an older Mn‐Cr age of 4562.9 ± 0.6 Ma for D'Orbigny relative to a Pb‐Pb age of 4557.8 ± 0.5 Ma for LEW and ADOR. One of the most unusual aspects of D'Orbigny is the presence of glass, a phase that has not been identified in any of the other angrites. The Mn‐Cr data for glass and a pyroxene fraction found in druses indicate that they formed contemporaneously with the main phases of the meteorite. Since the Mn‐Cr age of D'Orbigny is ?5 Ma years older than the angrites LEW and ADOR, D'Orbigny likely represents an earlier stage in the evolution of the angrite parent body.     

53Mn‐53Cr ages of Kaidun carbonates

Abstract– We report the ⁵³Mn‐⁵³Cr systematics of three dolomite grains from two different CI1 clasts contained within the Kaidun meteorite breccia. Three internal isochrones result in initial ⁵³Mn/⁵⁵Mn ratios of (4.2 ± 0.4) × 10^?6, (4.6 ± 1.3) × 10^?6, and (5.2 ± 1.1) × 10^?6. These initial values are consistent with those measured for dolomite in the Orgueil CI1 chondrite ( Hoppe et al. 2007 ; Petitat et al. 2009 ) but significantly lower than the initial ratio determined by Hutcheon et al. (1999) from a combination of different carbonate types within various lithologies of the Kaidun meteorite. We construct an accretion scenario for the Kaidun breccia by comparing the mineralogy and formation time scales of carbonates in the Kaidun CI1 lithologies to the analogous ones of the CI1 chondrite Orgueil. In Orgueil, dolomite precipitation precedes the formation of the first bruennerite grains by a few million years ( Hoppe et al. 2007 ; Petitat et al. 2009 ). As the CI1 clasts in Kaidun lack breunnerite grains, and considering that aqueous alteration occurred prior to reaccretion of the various clasts onto the Kaidun parent body (e.g., MacPherson et al. 2009 ), we hypothesize that after rapid accretion and early aqueous alteration occurring within the first approximately 4 Myr after solar system formation, impact disruption of several asteroids and their reassembly into the Kaidun parent asteroid was complete within an additional approximately 2 Myr. This confirms that aqueous alteration, impact, and reaccretion of material in the asteroid belt were early processes that began contemporaneously with chondrule formation.     

Nitrogen‐isotopic compositions of IIIE iron meteorites

Abstract— The (compositionally) closely related iron meteorite groups IIIE and IIIAB were originally separated based on differences in kamacite bandwidth, the presence of carbides only in the IIIE group, and marginally resolvable differences on the Ga‐Ni and Ge‐Ni diagrams. A total of six IIIE iron meteorites have been analyzed for C and N using secondary ion mass spectrometry, and three of these have also been analyzed for N, Ne, and Ar by stepped combustion. We show that these groups cannot be resolved on the basis of N abundances or isotopic compositions but that they are marginally different in C‐isotopic composition and nitride occurrence. Cosmic‐ray exposure age distributions of the IIIE and IIIAB iron meteorites seem to be significantly different. There is a significant N‐isotopic range among the IIIE iron meteorites. A negative correlation between δ15N and N concentration suggests that the increase in s?15N resulted from diffusional loss of N.     

Noble gases and nitrogen in Raghunathpura (IIAB) and Nyaung (IIIAB) iron meteorites

Noble gases and nitrogen were measured in two adjacent samples each from the Raghunathpura (IIAB) and the Nyaung (IIIAB) iron meteorite falls. Light noble gases in both the meteorites were of pure cosmogenic origin. Using (³He/⁴He)_c ratios and the production systematic of Ammon et al. ( 2009 ), we estimated the sample depth and meteoroid size for Nyaung (~8 cm depth in a ~15 cm radius object) and Raghunathpura (~12–14 cm depth in a ~25 cm object). We derived cosmic ray exposure ages of 1710 ± 256 Ma (for Nyaung, the highest reported so far for the IIIAB group) and 224 ± 34 Ma (for Raghunathpura). Variable amounts of trapped Kr and Xe were found in both meteorites. The phase Q‐like elemental ratio (⁸⁴Kr/¹³²Xe) suggests that the trapped component is of indigenous origin, and most likely hosted in the heterogeneously distributed micro‐inclusions of troilite/schreibersite. Trapped phase Q component is being reported for the first time, for a IIAB iron meteorite. Both meteorites showed light isotopic composition for nitrogen, and need at least two N components to explain the observed N isotopic systematic. Variable amounts of trapped noble gases and the presence of more than one N component suggest that the magmatic process that formed the parent body of these meteorites either could not completely homogenize or completely degas all the phases.     

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.     

40Ar‐39Ar chronology of lunar meteorites Northwest Africa 032 and 773

Abstract— The ⁴⁰Ar‐³⁹Ar dating technique has been applied to the lunar meteorites Northwest Africa 032 (NWA 032), an unbrecciated mare basalt, and Northwest Africa 773 (NWA 773), (composed of cumulate and breccia lithologies), to determine the crystallization age and timing of shock events these meteorites may have experienced. Stepped heating analyses of several different samples of NWA 032 gave complex age spectra but indistinguishable total ages with a mean of 2.779 ± 0.014 Gyr. Possible causes of the complex age spectra obtained from NWA 032 include recoil of ³⁹Ar, or the presence of pre‐shock ⁴⁰Ar incorporated into shock‐melt veins. The effects of shock veins were investigated by laser fusion of 20 small samples expected to contain varying proportions of the shock veins. The laser ages show a narrow age distribution between 2.61–2.86 Gyr and a mean of 2.73 ± 0.03 Gyr, identical to the total age of ?2.80 Gyr obtained for the bulk sample. Diffusion calculations based on the stepped heating data indicate that Ar release can be reconciled by release from feldspar (and possibly shock veins) at low temperatures followed by pyroxene at higher temperatures. The exposure age of NWA 032 is 212 ± 11 Myr, and it contains low trapped solar Ar. Stepped heating of cumulate and breccia portions of NWA 773 also give a relatively young age of 2.91 Gyr. The presence of trapped Ar in the breccia makes the age determination of this component less precise, but release of Ar appears to be from the same mineral phase, assumed to be plagioclase, in both lithologies. A marked difference in exposure age between the 2 lithologies also exists, with the breccia having spent 81 Myr longer at the lunar surface; this finding is consistent with the higher trapped Ar content of this lithology. Assuming that 2.80 Gyr and 2.91 Gyr are the crystallization ages of NWA 032 and NWA 773 respectively, these two meteorites are the youngest lunar mare basalts available for study.     

Testing an integrated chronology: I‐Xe analysis of enstatite meteorites and a eucrite

Abstract— We have determined initial ¹²⁹I/¹²⁷I ratios for mineral concentrates of four enstatite meteorites and a eucrite. In the case of the enstatite meteorites the inferred ages are associated with the pyroxene‐rich separates giving pyroxene closure ages relative to the Shallowater standard of Indarch (EH4, 0.04 ± 0.67 Ma), Khairpur (EL6, ?4.22 ± 0.67 Ma), Khor Temiki (aubrite, ?0.06 Ma), and Itqiy (enstatite achondrite, ?2.6 ± 2.6 Ma), negative ages indicate closure after Shallowater. No separate from the cumulate eucrite Asuka (A?) 881394 yielded a consistent ratio, though excess ¹²⁹Xe was observed in a feldspar separate, suggesting disturbance by thermal metamorphism within 25 Ma of closure in Shallowater. Iodine‐129 ages are mapped to the absolute Pb‐Pb time scale using the calibration proposed by Gilmour et al. (2006) who place the closure age of Shallowater at 4563.3 ± 0.4 Ma. Comparison of the combined ¹²⁹I‐Pb data with associated ⁵³Mn ages, for objects that have been dated by both systems, indicates that all three chronometers evolved concordantly in the early solar system. The enstatite chondrites are offset from the linear array described by asteroid‐belt objects when ⁵³Mn ages are plotted against combined ¹²⁹I‐Pb data, supporting the suggestion that ⁵³Mn was radially heterogeneous in the early solar system.     

The formation of IIE iron meteorites investigated by the chondrule‐bearing Mont Dieu meteorite

A 435 kg piece of the Mont Dieu iron meteorite (MD) contains cm‐sized silicate inclusions. Based on the concentration of Ni, Ga, Ge, and Ir (8.59 ± 0.32 wt%, 25.4 ± 0.9 ppm, 61 ± 2 ppm, 7.1 ± 0.4 ppm, respectively) in the metal host, this piece can be classified as a IIE nonmagmatic iron. The silicate inclusions possess a chondritic mineralogy and relict chondrules occur throughout the inclusions. Major element analysis, oxygen isotopic analysis (Δ¹⁷O = 0.71 ± 0.02‰), and mean Fa and Fs molar contents (Fa_{15.7 ± 0.4} and Fs_{14.4 ± 0.5}) indicate that MD originated as an H chondrite. Because of strong similarities with Netschaëvo IIE, MD can be classified in the most primitive subgroup of the IIE sequence. ⁴⁰Ar/³⁹Ar ages of 4536 ± 59 Ma and 4494 ± 95 Ma obtained on pyroxene and plagioclase inclusions show that MD belongs to the old (~4.5 Ga) group of IIE iron meteorites and that it has not been perturbed by any subsequent heating event following its formation. The primitive character of MD sheds light on the nature of its formation process, its thermal history, and the evolution of its parent body.     

Raman spectroscopic properties and Raman identification of CaS‐MgS‐MnS‐FeS‐Cr2FeS4 sulfides in meteorites and reduced sulfur‐rich systems

Raman spectra were acquired on a series of natural and synthetic sulfide minerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite ((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr₂FeS₄). Natural samples come from three enstatite chondrites, three aubrites, and one anomalous ungrouped enstatite meteorite. Synthetic samples range from pure endmembers (CaS, FeS, MgS) to complex solid solutions (Fe, Mg, Ca)S. The main Raman peaks are localized at 225, 285, 360, and 470 cm^?1 for the Mg‐rich sulfides; at 185, 205, and 285 cm^?1 for the Ca‐rich sulfides; at 250, 370, and 580 cm^?1 for the Mn‐rich sulfides; at 255, 290, and 365 cm^?1 for the Cr‐rich sulfides; and at 290 and 335 cm^?1 for troilite with, occasionally, an extra peak at 240 cm^?1. A peak at 160 cm^?1 is present in all Raman spectra and cannot be used to discriminate between the different sulfide compositions. According to group theory, none of the cubic monosulfides oldhamite, niningerite, or alabandite should present first‐order Raman spectra because of their ideal rocksalt structure. The occurrence of broad Raman peaks is tentatively explained by local breaking of symmetry rules. Measurements compare well with the infrared frequencies calculated from first‐principles calculations. Raman spectra arise from activation of certain vibrational modes due to clustering in the solid solutions or to coupling with electronic transitions in semiconductor sulfides.     

Laboratory experiments on the weathering of iron meteorites and carbonaceous chondrites by iron‐oxidizing bacteria

Abstract— Batch culture experiments were performed to investigate the weathering of meteoritic material by iron‐oxidizing bacteria. The aerobic, acidophilic iron oxidizer (A. ferrooxidans) was capable of oxidizing iron from both carbonaceous chondrites (Murchison and Cold Bokkeveld) and iron meteorites (York and Casas Grandes). Preliminary iron isotope results clearly show contrasted iron pathways during oxidation with and without bacteria suggesting that a biological role in meteorite weathering could be distinguished isotopically. Anaerobic iron‐oxidizers growing under pH‐neutral conditions oxidized iron from iron meteorites. These results show that rapid biologically‐mediated alteration of extraterrestrial materials can occur in both aerobic and anaerobic environments. These results also demonstrate that iron can act as a source of energy for microorganisms from both iron and carbonaceous chondrites in aerobic and anaerobic conditions with implications for life on the early Earth and the possible use of microorganisms to extract minerals from asteroidal material.     

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.     

The Cu isotopic composition of iron meteorites

Abstract– High‐precision Cu isotopic compositions have been measured for the metal phase of 29 iron meteorites from various groups and for four terrestrial standards. The data are reported as the δ⁶⁵Cu permil deviation of the ⁶⁵Cu/⁶³Cu ratio relative to the NIST SRM 976 standard. Terrestrial mantle rocks have a very narrow range of variations and scatter around zero. In contrast, iron meteorites show δ⁶⁵Cu approximately 2.3‰ variations. Different groups of iron meteorites have distinct δ⁶⁵Cu values. Nonmagmatic IAB‐IIICD iron meteorites have similar δ⁶⁵Cu (0.03 ± 0.08 and 0.12 ± 0.10, respectively), close to terrestrial values (approximately 0). The other group of nonmagmatic irons, IIE, is isotopically distinct (?0.69 ± 0.15). IVB is the iron meteorite group with the strongest elemental depletion in Cu and samples in this group are enriched in the lighter isotope (δ⁶⁵Cu down to ?2.26‰). Evaporation should have produced an enrichment in ⁶⁵Cu over ⁶³Cu (δ⁶⁵Cu >0) and can therefore be ruled out as a mechanism for volatile loss in IVB meteorites. In silicate‐bearing iron meteorites, Δ¹⁷O correlates with δ⁶⁵Cu. This correlation between nonmass‐dependent and mass‐dependent parameters suggests that the Cu isotopic composition of iron meteorites has not been modified by planetary differentiation to a large extent. Therefore, Cu isotopic ratios can be used to confirm genetic links. Cu isotopes thus confirm genetic relationships between groups of iron meteorites (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites). Several genetic connections between iron meteorites groups are confirmed by Cu isotopes, (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites).     

High‐pressure minerals in shocked meteorites

Heavily shocked meteorites contain various types of high‐pressure polymorphs of major minerals (olivine, pyroxene, feldspar, and quartz) and accessory minerals (chromite and Ca phosphate). These high‐pressure minerals are micron to submicron sized and occur within and in the vicinity of shock‐induced melt veins and melt pockets in chondrites and lunar, howardite–eucrite–diogenite (HED), and Martian meteorites. Their occurrence suggests two types of formation mechanisms (1) solid‐state high‐pressure transformation of the host‐rock minerals into monomineralic polycrystalline aggregates, and (2) crystallization of chondritic or monomineralic melts under high pressure. Based on experimentally determined phase relations, their formation pressures are limited to the pressure range up to ~25 GPa. Textural, crystallographic, and chemical characteristics of high‐pressure minerals provide clues about the impact events of meteorite parent bodies, including their size and mutual collision velocities and about the mineralogy of deep planetary interiors. The aim of this article is to review and summarize the findings on natural high‐pressure minerals in shocked meteorites that have been reported over the past 50 years.     

Mineralogical and chemical composition and cosmic‐ray exposure history of two mesosiderites and two iron meteorites

Abstract— We performed a comprehensive study of the noble gas isotopic abundances, radionuclide activities, and mineralogical and chemical composition of two mesosiderites and two iron meteorites. For the mesosiderites Dong Ujimqin Qi and Weiyuan, the silicate and the metal phases were studied. The anomalous ataxite Rafrüti is not chemically related to any other meteorite class, whereas Ningbo is a type IVA octahedrite. The mineralogy and major and trace element abundances of the silicate phases of Dong Ujimqin Qi and Weiyuan are similar to those of other mesosiderites and distinct from those of the howardites. The cosmic‐ray exposure history was studied based on the concentrations of the cosmogenic noble gas nuclei and radionuclide activities. For the iron meteorites, cosmic‐ray exposure ages were calculated from the pairs ¹⁰Be‐²¹Ne, ²⁶Al‐²¹Ne, and ³⁶Cl‐³⁶Ar. Rafrüti yields the youngest exposure age of all ataxites (6.8 ± 1.7 Ma), whereas that of Ningbo with 107 ± 15 Ma falls within the range observed for the other octahedrites. The parent body break‐up times of the mesosiderites Dong Ujimqin Qi and Weiyuan are 252 ± 50 and 25.9 ± 5.0 Ma, respectively. We find no evidence for a common break‐up event for the mesosiderites and the howardites.     

Formation of the Treysa quintet and the main‐group pallasites by impact‐generated processes in the IIIAB asteroid

Treysa and Delegate have compositions closely similar to those of IIIAB irons but plot above the IIIAB field on Ir‐Au diagrams; for this reason they are designated anomalous members of IIIAB. All refractory siderophiles share this anomaly. Wasson ( 1999 ) interpreted the large spread on IIIAB Ir‐Au diagrams to result from melt‐trapping and generated solid and liquid fractional crystallization tracks; almost all IIIAB irons fall between the tracks. In contrast, Treysa, Delegate, and three other irons (the Treysa quintet) plot beyond the liquid track. Ideal fractional crystallization cannot account for compositions that plot outside the region between the tracks. Possible explanations for the anomalous compositions of the Treysa quintet are that (1) these meteorites did not form in the IIIAB magma or (2) they formed by the mixing of early crystallized solids with a late liquid. The weight of the evidence including cosmic‐ray ages favor the second explanation. Although this explanation can account for positions plotting above the liquid track, it requires special circumstances. The infalling blocks must be assimilated and the resulting melt must crystallize quickly into pockets small enough (<1 m) to allow igneous gradients to be leveled by subsequent diffusion. The Treysa quintet shares the region beyond the liquid track with most main‐group pallasites (PMG), which may have also originated in the IIIAB body. It appears that Treysa, its relatives, and the PMG were formed in one or more impact events that mixed olivine and solid metal formed near the core‐mantle boundary with nearby magma. It is then necessary to cool the melt rapidly; the best way to achieve rapid cooling is by heat exchange with cooler solids. That the Treysa quintet and the PMG can be explained by the same processes operating on late IIIAB magma supports the conclusion that PMG formed on the IIIAB parent asteroid.     

Revisiting spectral parameters of silicate‐bearing meteorites

Abstract— Visible and near‐infrared reflectance spectra of a sample of silicate‐bearing meteorites have been used to evaluate the spectral parameters space defined in the pioneering work of Gaffey et al. (1993). The studied sample consisted of 91 ordinary chondrites, 47 basaltic achondrites, and 21 different laboratory mixtures obtained from the RELAB database. Our results indicate that the spectral parameter space, in particular the BAR versus band I center, is not suitable enough to identify the mineralogy of meteorites and asteroids. The grain size of the sample also appears as a very sensitive parameter and can play an important role in locating an object in the spectral parameter space. Finally, the application of our study to the question of a genetic link between V‐type asteroids and HED meteorites shows that these bodies plot in distinct regions in the BAR versus band I center space. This result further confirms that those spectral parameters cannot uniquely define the mineralogy of a sample.     

53Mn‐53Cr dating of aqueously formed carbonates in the CM2 lithology of the Sutter's Mill carbonaceous chondrite

Radiometric dating of secondary minerals can be used to constrain the timing of aqueous alteration on meteoritic parent bodies. Dolomite is a well‐documented secondary mineral in CM chondrites, and is thought to have formed by precipitation from an aqueous fluid on the CM parent body within several million years of accretion. The petrographic context of crosscutting dolomite veins indicates that aqueous alteration occurred in situ, rather than in the nebular setting. Here, we present ⁵³Mn‐⁵³Cr systematics for dolomite grains in Sutter's Mill section SM51‐1. The Mn‐Cr isotope data show well‐resolved excesses of ⁵³Cr correlated with ⁵⁵Mn/⁵²Cr ratio, which we interpret as evidence for the in situ decay of radioactive ⁵³Mn. After correcting for the relative sensitivities of Mn and Cr using a synthetic Mn‐ and Cr‐bearing calcite standard, the data yield an isochron with slope corresponding to an initial ⁵³Mn/⁵⁵Mn ratio of 3.42 ± 0.86 × 10^?6. The reported error includes systematic uncertainty from the relative sensitivity factor. When calculated relative to the U‐corrected Pb‐Pb absolute age of the D'Orbigny angrite, Sutter's Mill dolomites give a formation age between 4564.8 and 4562.2 Ma (2.4–5.0 Myr after the birth of the solar system). This age is contemporaneous with previously reported ages for secondary carbonates in CM and CI chondrites. Consistent carbonate precipitation ages between the carbonaceous chondrite groups suggest that aqueous alteration was a common process during the early stages of parent body formation, probably occurring via heating from internal ²⁶Al decay. The high‐precision isochron for Sutter's Mill dolomite indicates that late‐stage processing did not reach temperatures that were high enough to further disturb the Mn‐Cr isochron.     

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.