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).     

Mass‐dependent fractionation of nickel isotopes in meteoritic metal

Abstract— We measured nickel isotopes via multicollector inductively coupled plasma mass spectrometry (MC‐ICPMS) in the bulk metal from 36 meteorites, including chondrites, pallasites, and irons (magmatic and non‐magmatic). The Ni isotopes in these meteorites are mass fractionated; the fractionation spans an overall range of ～0.4‰ amu^?1. The ranges of Ni isotopic compositions (relative to the SRM 986 Ni isotopic standard) in metal from iron meteorites (～0.0 to ～0.3‰ amu^?1) and chondrites (～0.0 to ～0.2‰ amu^?1) are similar, whereas the range in pallasite metal (～–0.1 to 0.0‰ amu^?1) appears distinct. The fractionation of Ni isotopes within a suite of fourteen IIIAB irons (～0.0 to ～0.3‰ amu^?1) spans the entire range measured in all magmatic irons. However, the degree of Ni isotopic fractionation in these samples does not correlate with their Ni content, suggesting that core crystallization did not fractionate Ni isotopes in a systematic way. We also measured the Ni and Fe isotopes in adjacent kamacite and taenite from the Toluca IAB iron meteorite. Nickel isotopes show clearly resolvable fractionation between these two phases; kamacite is heavier relative to taenite by ～0.4‰ amu^?1. In contrast, the Fe isotopes do not show a resolvable fractionation between kamacite and taenite. The observed isotopic compositions of kamacite and taenite can be understood in terms of kinetic fractionation due to diffusion of Ni during cooling of the Fe‐Ni alloy and the development of the Widmanstätten pattern.     

Nitrogen components in IAB/IIICD iron meteorites

Abstract— Isotopic variations have been reported for many elements in iron meteorites, with distinct N signatures found in the metal and graphite of IAB irons. In this study, a dozen IAB/IIICD iron meteorites (see Table 1 for new classifications) were analyzed by stepwise pyrolysis to resolve nitrogen components. Although isotopic heterogeneity has been presumed to be lost in thermally processed parent objects, the high‐resolution nitrogen isotopic data indicate otherwise. At least one reservoir has a light nitrogen signature, δ¹⁵N = ?(74 ± 2)‰, at 900 °C to 1000 °C, with a possible second, even lighter, reservoir in Copiapo (δ¹⁵N ≤ ?82‰). These releases are consistent with metal nitride decomposition or low‐temperature metal phase changes. Heavier nitrogen reservoirs are observed in steps ≤700 °C and at 1200 °C to 1400 °C. The latter release has a δ¹⁵N signature with a limit of ≥?16‰. Xenon isotopic signatures are sensitive indicators for the presence of inclusions because of the very low abundances of Xe in metal. The combined high‐temperature release shows ¹³¹Xe and ¹²⁹Xe excesses to be consistent with shifts expected for Te(n,γ) reaction in troilite by epithermal neutrons, but there are also possible alterations in the isotopic ratios likely due to extinct ¹²⁹I and cosmic‐ray spallation. The IAB/IIICD iron data imply that at least one light N component survived the formation processes of iron parent objects which only partially exchanged nitrogen between phases. Preservation of separate N reservoirs conflicts with neither the model of impact‐heating effects for these meteorites nor reported age differences between metal and silicates.     

Mn‐Cr chronology of five IIIAB iron meteorites

Abstract— Mn‐Cr systematics in phosphates (sarcopside, graftonite, beusite, galileiite, and johnsomervilleite) in IIIAB iron meteorites were investigated by secondary ion mass spectrometry (SIMS). In most cases, excesses in ⁵³Cr are found and δ⁵³Cr is well correlated with Mn/Cr ratios, suggesting that ⁵³Mn was alive at the time of IIIAB iron formation. The inferred Mn‐Cr “ages” are different for different phosphate minerals. This is presumably due to a combined effect of the slow cooling rates of IIIAB iron meteorites and the difference in the diffusion properties of Cr and Mn in the phosphates. The ages of sarcopside are the same for the IIIAB iron meteorites. Johnsomervilleite shows apparent old ages, probably because of a gain of Cr enriched in ⁵³Cr during the closure process. Apparently, old Mn‐Cr ages reported in previous studies can also be explained in a similar way. Therefore, the IIIAB iron meteorites probably experienced identical thermal histories and thus derived from the core of a parent body. Thermal histories of the parent body of IIIAB iron meteorites that satisfy the Mn‐Cr chronology and metallographic cooling rates were constructed by computer simulation. The thermal history at an early stage (<10 Ma after CAI formation) is well determined, though later history may be more model‐dependent. It is suggested that relative timing of various events in the IIIAB parent body may be estimated with the aid of the thermal history. There is a systematic difference in Mn and Cr concentrations in various minerals (phosphates, sulfide, etc.) among the IIIAB iron meteorites, which seems to be mainly controlled by redox conditions.     

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.     

Tungsten isotopes in bulk meteorites and their inclusions—Implications for processing of presolar components in the solar protoplanetary disk

We present high precision, low‐ and high‐resolution tungsten isotope measurements of iron meteorites Cape York (IIIAB), Rhine Villa (IIIE), Bendego (IC), and the IVB iron meteorites Tlacotepec, Skookum, and Weaver Mountains, as well as CI chondrite Ivuna, a CV3 chondrite refractory inclusion (CAI BE), and terrestrial standards. Our high precision tungsten isotope data show that the distribution of the rare p‐process nuclide ¹⁸⁰W is homogeneous among chondrites, iron meteorites, and the refractory inclusion. One exception to this pattern is the IVB iron meteorite group, which displays variable excesses relative to the terrestrial standard, possibly related to decay of rare ¹⁸⁴Os. Such anomalies are not the result of analytical artifacts and cannot be caused by sampling of a protoplanetary disk characterized by p‐process isotope heterogeneity. In contrast, we find that ¹⁸³W is variable due to a nucleosynthetic s‐process deficit/r‐process excess among chondrites and iron meteorites. This variability supports the widespread nucleosynthetic s/r‐process heterogeneity in the protoplanetary disk inferred from other isotope systems and we show that W and Ni isotope variability is correlated. Correlated isotope heterogeneity for elements of distinct nucleosynthetic origin (¹⁸³W and ⁵⁸Ni) is best explained by thermal processing in the protoplanetary disk during which thermally labile carrier phases are unmixed by vaporization thereby imparting isotope anomalies on the residual processed reservoir.     

Mineral and chemical composition of the new iron meteorite Javorje from Slovenia

Abstract– The single‐piece iron meteorite Javorje, with a mass of 4920 g, is the heaviest and largest meteorite found in the territory of Slovenia. The meteorite Javorje is a medium octahedrite with kamacite bandwidth of 0.85 ± 0.26 mm. The bulk composition of Ni (7.83 wt%), Co (0.48 wt%) and trace elements Ga (25 μg/g), Ge (47 μg/g), Ir (7.6 μg/g), As (5.8 μg/g), Au (0.47 μg/g), and Pt (13.4 μg/g) indicates that the meteorite Javorje belongs to the chemical group IIIAB. Mineral and bulk chemical compositions are consistent with other reported group IIIAB meteorites. The presence of numerous rhabdites, carlsbergite, sparse troilite, and chromite and abundance of daubréelites are in accordance with low‐Ni and low‐P IIIAB iron meteorites. The severely weathered surface and secondary weathering products in the interior of the meteorite suggest its high terrestrial age.     

Ion probe measurements of carbon and nitrogen in iron meteorites

Abstract— Carbon and nitrogen distributions in iron meteorites, their concentrations in various phases, and their isotopic compositions in certain phases were measured by secondary ion mass spectrometry (SIMS). Taenite (and its decomposition products) is the main carrier of C, except for IAB iron meteorites, where graphite and/or carbide (cohenite) may be the main carrier. Taenite is also the main carrier of N in most iron meteorites unless nitrides (carlsbergite CrN or roaldite (Fe, Ni)₄N) are present. Carbon and N distributions in taenite are well correlated unless carbides and/or nitrides are exsolved. There seem to be three types of C and N distributions within taenite. (1) These elements are enriched at the center of taenite (convex type). (2) They are enriched at the edge of taenite (concave type). (3) They are enriched near but some distance away from the edge of taenite (complex type). The first case (1) is explained as equilibrium distribution of C and N in Fe-Ni alloy with M-shape Ni concentration profile. The second case (2) seems to be best explained as diffusion controlled C and N distributions. In the third case (3), the interior of taenite has been transformed to the α phase (kamacite or martensite). Carbon and N were expelled from the α phase and enriched near the inner border of the remaining γ phase. Such differences in the C and N distributions in taenite may reflect different cooling rates of iron meteorites. Nitrogen concentrations in taenite are quite high approaching 1 wt% in some iron meteorites. Nitride (carlsbergite and roaldite) is present in meteorites with high N concentrations in taenite, which suggests that the nitride was formed due to supersaturation of the metallic phases with N. The same tendency is generally observed for C (i.e., high C concentrations in taenite correlate with the presence of carbide and/or graphite). Concentrations of C and N in kamacite are generally below detection limits. Isotopic compositions of C and N in taenite can be measured with a precision of several permil. Isotopic analysis in kamacite in most iron meteorites is not possible because of the low concentrations. The C isotopic compositions seem to be somewhat fractionated among various phases, reflecting closure of C transport at low temperatures. A remarkable isotopic anomaly was observed for the Mundrabilla (IIICD anomalous) meteorite. Nitrogen isotopic compositions of taenite measured by SIMS agree very well with those of the bulk samples measured by conventional mass spectrometry.     

New Chilean iron meteorites: Medium octahedrites from Northern Chile are unique

Abstract— We report data on three new iron meteorites from Northern Chile and propose names. All are unnamed iron meteorites from the meteorite collection at the Universidad de La Serena. For two, the provenance is unknown; for the third, the presumed discovery site is in the countryside east of Iquique. The three meteorites have been analyzed by instrumental neutron activation analysis (INAA) and their structures examined with a binocular microscope. La Serena is a complete 663 g iron, a new member of group IIICD; it is not paired with any other iron. Elqui has a mass of 260 g; two faces are fractures, possibly produced by human actions, but fusion crust appears to be present on some of the remaining surface. It is a hexahedrite and a member of group IIAB, but its composition differs from that of all other Chilean hexahedrites. The third iron, Pozo Almonte, is a medium octahedrite member of group IIIAB, one of the most common meteorite groups. To find out whether it is paired, we assembled a full set of IIIAB iron meteorites from Northern Chile. Our compositional data show that Pozo Almonte is not paired with any other IIIAB iron, and that there are no pairings within the full set with the possible exception of Joel's Iron and Sierra Sandon, which differ only in their contents of Ir, 0.39 and 0.34 μg/g, respectively. However, Buchwald's (1975) structural observations rule out this possible pairing. We find appreciable differences in Cu, As and Au between the previously paired IIIAB irons Chañaral and Ilimaës and conclude that these should not be paired.     

The pyroxene pallasites,Vermillion and Yamato 8451: Not quite a couple

Abstract— Two pallasites, Vermillion and Yamato (Y)‐8451, have been studied to obtain petrologic, trace element, and O‐isotopic data. Both meteorites contain low‐Ca and high‐Ca pyroxenes (<2% by volume) and have been dubbed “pyroxene pallasites.” Pyroxene occurs as large individual grains, as inclusions in olivine and in other pyroxene, and as grains along the edges of olivine. Symplectic overgrowths, sometimes found in Main Group and Eagle Station pallasites, are not seen in the pyroxene pallasites. Olivine compositions are Fa_10–12, similar to those of Main Group pallasites. Siderophile trace element data show that metal in the two meteorites have significantly differing compositions that are, for many elements, outside the range of the Main Group and Eagle Station pallasites. These compositions also differ from those of IAB and IIIAB iron meteorites. Rare earth element (REE) patterns in merrillite are similar to those seen in other pallasites, indicating formation by subsolidus reaction between metal and silicate, with the merrillite inheriting its pattern from the surrounding silicates. The O‐isotopic compositions of Vermillion and Y‐8451 are similar but differ from Main Group or Eagle Station pallasites, as well as other achondrite and primitive achondrite groups. Although Vermillion and Y‐8451 have similar mineralogy, pyroxene compositions, REE patterns, and O‐isotopic compositions, there is sufficient evidence to resist formally grouping these two meteorites. This evidence includes the texture of Vermillion, siderophile trace element data, and the presence of cohenite in Vermillion.     

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

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

Ulasitai: A new iron meteorite likely paired with Armanty (IIIE)

Abstract— The Ulasitai iron was recently found about 130 km southeast to the find site of the Armanty (Xinjiang, IIIE) meteorite. It is a coarse octahedrite with a kamacite bandwidth of 1.2 ± 0.2 (0.9–1.8) mm. Plessite is abundant, as is taenite, kamacite, cohenite, and schreibersite with various microstructures. Schreibersite is Ni‐rich (30.5–55.5 wt%) in plessite or coexisting with troilite and daubreelite, in comparison with the coarse laths (20.6–21.2 wt%) between the Widmanstätten pattern plates. The correlation between the center Ni content and the half bandwidth of taenite suggest a cooling rate of ?20 °C/Myr based on simulations. The petrography and mineral chemistry of Ulasitai are similar to Armanty. The bulk samples of Ulasitai were measured, together with Armanty, Nandan (IIICD), and Mundrabilla (IIICD), by inductively coupled plasma atomic emission spectrometry (ICP‐AES) and mass spectrometry (ICP‐MS). The results agree with literature data of the same meteorites, and our analyses of four samples of Armanty (L1, L12, L16, L17) confirm a homogeneous composition (Wasson et al. 1988). The bulk composition of Ulasitai is identical to that of Armanty, both plotting within the IIIE field. We classify Ulasitai as a new IIIE iron and suggest that it pairs with Armanty.     

Diffusion‐driven kinetic isotope effect of Fe and Ni during formation of the Widmanstätten pattern

Abstract— Iron meteorites show resolvable Fe and Ni isotopic fractionation between taenite and kamacite. For Toluca (IAB), the isotopic fractionations between the two phases are around +0.1‰/amu for Fe and ?0.4‰/amu for Ni. These variations may be due to i) equilibrium fractionation, ii) differences in the diffusivities of the different isotopes, or iii) a combination of both processes. A computer algorithm was developed in order to follow the growth of kamacite out of taenite during the formation of the Widmanstätten pattern as well as calculate the fractionation of Fe and Ni isotopes for a set of cooling rates ranging from 25 to 500 °C/Myr. Using a relative difference in diffusion coefficients of adjacent isotopes of 4‰/amu for Fe and Ni (β = 0.25), the observations made in Toluca can be reproduced for a cooling rate of 50 °C/Myr. This value agrees with earlier cooling rate estimates based on Ni concentration profiles. This supports the idea that the fractionation measured for Fe and Ni in iron meteorites is driven by differences in diffusivities of isotopes. It also supports the validity of the value of 0.25 adopted for β for diffusion of Fe and Ni in Fe‐Ni alloy in the temperature range of 400–700 °C.     

Trace Element Partitioning between Taenite and Kamacite; Relationship to the Cooling Rates of Iron Meteorites

Abstract— Instrumental neutron activation analysis (INAA) was used to determine Ni, Co, Cu, Ga, As, Au, W, Re and Ir in taenite lamellae isolated by acid dissolution from eight iron meteorites from groups IA, IIIAB and IVA. Taenite is enriched in Ni, Cu, Ga, As, Au, W, Re and Ir relative to kamacite, whereas taenite is depleted in Co. Taenite/kamacite partition ratios in slowly cooled IAB meteorites are farther from unity than those in rapidly cooled IVA meteorites. Taenite/kamacite partition ratios for Cu, Ir, Au and Co may be sensitive cooling rate indicators.     

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.     

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.     

A detailed mineralogical,petrographic, and geochemical study of the highly reduced chondrite,Acfer 370

Among the many ungrouped meteorites, Acfer 370, NWA 7135, and El Médano 301—probably along with the chondritic inclusion in Cumberland Falls and ALHA 78113—represent a homogeneous grouplet of strongly reduced forsterite‐rich chondrites characterized by common textural, chemical, mineralogical, and isotopic features. All of these meteorites are much more reduced than OCs, with a low iron content in olivine and low‐Ca pyroxene. In particular, Acfer 370 is a type 4 chondrite that has olivine and low‐Ca pyroxene compositional ranges of Fa 5.2–5.8 and Fs 9.4–33.4, respectively. The dominant phase is low‐Ca pyroxene (36.3 vol%), followed by Fe‐Ni metal (16.3 vol%) and olivine (15.5 vol%); nevertheless, considering the Fe‐oxyhydroxide (due to terrestrial weathering), the original metal content was around 29.6 vol%. Finally, the mean oxygen isotopic composition Δ¹⁷O = +0.68‰ along with the occurrence of a silica phase, troilite, Ni‐rich phosphides, chromite, and oldhamite confirms that these ungrouped meteorites have been affected by strong reduction and are different from any other group recognized so far.     

Variations in impact effects among IIIE iron meteorites

Group‐IIIE iron meteorites can be ordered into four categories reflecting increasing degrees of shock alteration. Weakly shocked samples (Armanty, Colonia Obrera, Coopertown, Porto Alegre, Rhine Villa, Staunton, and Tanokami Mountain) have haxonite within plessite, unrecrystallized kamacite grains containing Neumann lines or possessing the ? structure, and sulfide inclusions typically consisting of polycrystalline troilite with daubréelite exsolution lamellae. The only moderately shocked sample is NWA 4704, in which haxonite has been partially decomposed to graphite; the majority of the kamacite in NWA 4704 is recrystallized, and its sulfide inclusions were partly melted. Strongly shocked samples (Cachiyuyal, Kokstad, and Paloduro) contain graphite and no haxonite, suggesting that pre‐existing haxonite fully decomposed. Also present in these rocks are recrystallized kamacite and melted troilite. Residual heat from the impact caused annealing and recrystallization of kamacite as well as the decomposition of haxonite into graphite. Severely shocked samples (Aliskerovo and Willow Creek) have sulfide‐rich assemblages consisting of fragmental and subhedral daubréelite crystals, 1–4 vol% spidery troilite filaments, and 30–50 vol% low‐Ni kamacite grains, some of which contain up to 6.0 wt% Co; haxonite in these inclusions has fully decomposed to graphite. The wide range of impact effects in IIIE irons is attributed to one or more major collision(s) on the parent asteroid that affected different group members to different extents depending on their proximity to the impact point.     

The formation of the Widmanstätten structure in meteorites

Abstract— We have evaluated various mechanisms proposed for the formation of the Widmanstätten pattern in iron meteorites and propose a new mechanism for low P meteoritic metal. These mechanisms can also be used to explain how the metallic microstructures developed in chondrites and stony‐iron meteorites. The Widmanstätten pattern in high P iron meteorites forms when meteorites enter the three‐phase field α + γ + Ph via cooling from the γ + Ph field. The Widmanstätten pattern in low P iron meteorites forms either at a temperature below the (α + γ)/(α + γ + Ph) boundary or by the decomposition of martensite below the martensite start temperature. The reaction γ → α + γ, which is normally assumed to control the formation of the Widmanstätten pattern, is not applicable to the metal in meteorites. The formation of the Widmanstätten pattern in the vast majority of low P iron meteorites (which belong to chemical groups IAB‐IIICD, IIIAB, and IVA) is controlled by mechanisms involving the formation of martensite α₂. We propose that the Widmanstätten structure in these meteorites forms by the reaction γ → α₂ + γ → α + γ, in which α₂ decomposes to the equilibrium α and γ phases during the cooling process. To determine the cooling rate of an individual iron meteorite, the appropriate formation mechanism for the Widmanstätten pattern must first be established. Depending on the Ni and P content of the meteorite, the kamacite nucleation temperature can be determined from either the (γ + Ph)/(α + γ + Ph) boundary, the (α + γ)/(α + γ + Ph) boundary, or the M_s temperature. With the introduction of these three mechanisms and the specific phase boundaries and the temperatures where transformations occur, it is no longer necessary to invoke arbitrary amounts of under‐cooling in the calculation of the cooling rate. We conclude that martensite decomposition via the reactions γ → α₂ → α + γ and γ → α₂ + γ → α + γ are responsible for the formation of plessite in irons and the metal phases of mesosiderites, chondrites, and pallasites. The hexahedrites (low P members of chemical group IIAB) formed by the massive transformation through the reaction γ → α_m → α at relatively high temperature in the two‐phase α + γ region of the Fe‐Ni‐P phase diagram near the α/(α + γ) phase boundary.     

Differentiation of metal‐rich meteoritic parent bodies: I. Measurements of PGEs,Re, Mo,W, and Au in meteoritic Fe‐Ni metal

Abstract— We describe an analytical technique for measurements of Fe, Ni, Co, Mo, Ru, Rh, W, Re, Os, Ir, Pt, and Au in bulk samples of iron meteorites. The technique involves EPMA (Fe, Ni, Co) and LA‐ICP‐MS analyses of individual phases of iron meteorites, followed by calculation of bulk compositions based on the abundances of these phases. We report, for the first time, a consistent set of concentrations of Mo, Ru, Rh, Pd, W, Re, Os, Ir, Pt, and Au in the iron meteorites Arispe, Bennett County, Grant, Cape of Good Hope, Cape York, Carbo, Chinga, Coahuila, Duchesne, Gibeon, Henbury, Mundrabilla, Negrillos, Odessa, Sikhote‐Alin, and Toluca and the Divnoe primitive achondrite. The comparison of our LA‐ICP‐MS data for a number of iron meteorites with high‐precision isotope dilution and INAA data demonstrates the good precision and accuracy of our technique. The narrow ranges of variations of Mo and Pd concentrations within individual groups of iron meteorites suggest that these elements can provide important insights into the evolution of parent bodies of iron meteorites. Under certain assumptions, the Mo concentrations can be used to estimate mass fractions of the metal‐sulfide cores in the parent bodies of iron meteorites. It appears that a range of Pd variations within a group of iron meteorites can serve as a useful indicator of S content in the core of its parent body.