The origin of the unique achondrite Northwest Africa 6704: Constraints from petrology, chemistry and Re-Os, O and Ti isotope systematics.

Northwest Africa (NWA) 6704 is a unique achondrite characterized by a near-chondritic major element composition with a remarkably intact igneous texture. To investigate the origin of this unique achondrite, we have conducted a combined petrologic, chemical, and 187Re-187Os, O, and Ti isotopic study. The meteorite consists of orthopyroxene megacrysts (En55-57Wo3-4Fs40-42; Fe/Mn = 1.4) up to 1.7 cm in length with finer interstices of olivine (Fa50-53; Fe/Mn = 1.1-2.1), chromite (Cr# ~ 0.94), awaruite, sulfides, plagioclase (Ab92An5Or3) and merrillite. The results of morphology, lattice orientation analysis, and mineral chemistry indicate that orthopyroxene megacrysts were originally hollow dendrites that most likely crystallized under high super-saturation and super-cooling conditions (1-102 °C/h), whereas the other phases crystallized between branches of the dendrites in the order of awaruite, chromite → olivine → merrillite → plagioclase. In spite of the inferred high supersaturation, the remarkably large size of orthopyroxene can be explained as a result of crystallization from a melt containing a limited number of nuclei that are preserved as orthopyroxene megacryst cores having high Mg# or including vermicular olivine. The Re-Os isotope data for bulk and metal fractions yield an isochron age of 4576 ± 250 Ma, consistent with only limited open system behavior of highly siderophile elements (HSE) since formation. The bulk chemical composition is characterized by broadly chondritic absolute abundances and only weakly fractionated chondrite-normalized patterns for HSE and rare earth elements (REE), together with substantial depletion of highly volatile elements relative to chondrites. The HSE and REE characteristics indicate that the parental melt and its protolith had not undergone significant segregation of metals, sulfides, or silicate minerals. These combined results suggest that a chondritic precursor to NWA 6704 was heated well above its liquidus temperature so that highly volatile elements were lost and the generated melt initially contained few nuclei of relict orthopyroxene, but the melting and subsequent crystallization took place on a timescale too short to allow magmatic differentiation. Such rapid melting and crystallization might occur as a result of impact on an undifferentiated asteroid. The O-Ti isotope systematics (Δ17O = -1.052 ± 0.004, 2 SD; ε50Ti = 2.28 ± 0.23, 2 SD) indicate that the NWA 6704 parent body sampled the same isotopic reservoirs in the solar nebula as the carbonaceous chondrite parent bodies. This is consistent with carbonaceous chondrite-like refractory element abundances and oxygen fugacity (FMQ = -2.6) in NWA 6704. Yet, the Si/Mg ratio of NWA 6704 is remarkably higher than those of carbonaceous chondrites, suggesting significant nebular fractionation of forsterite in its provenance.

Siderophile element constraints on the thermal history of the H chondrite parent body.

The abundances of highly siderophile elements (HSE: Re, Os, Ir, Ru, Pt, Pd), as well as 187Re-187Os and 182Hf-182W isotopic systematics were determined for separated metal, slightly magnetic, and nonmagnetic fractions from seven H4 to H6 ordinary chondrites. The HSE are too abundant in nonmagnetic fractions to reflect metal-silicate equilibration. The disequilibrium was likely a primary feature, as 187Re-187Os data indicate only minor open-system behavior of the HSE in the slightly and non-magnetic fractions. 182Hf-182W data for slightly magnetic and nonmagnetic fractions define precise isochrons for most meteorites that range from 5.2 ± 1.6 Ma to 15.2 ± 1.0 Ma after calcium aluminum inclusion (CAI) formation. By contrast, 182W model ages for the metal fractions are typically 2-5 Ma older than the slope-derived isochron ages for their respective, slightly magnetic and nonmagnetic fractions, with model ages ranging from 1.4 ± 0.8 Ma to 12.6 ± 0.9 Ma after CAI formation. This indicates that the W present in the silicates and oxides was not fully equilibrated with the metal when diffusive transport among components ceased, consistent with the HSE data. Further, the W isotopic compositions of size-sorted metal fractions from some of the H chondrites also differ, indicating disequilibrium among some metal grains. The chemical/isotopic disequilibrium of siderophile elements among H chondrite components is likely the result of inefficient diffusion of siderophile elements from silicates and oxides to some metal and/or localized equilibration as H chondrites cooled towards their respective Hf-W closure temperatures. The tendency of 182Hf-182W isochron ages to young from H5 to H6 chondrites may indicate derivation of these meteorites from a slowly cooled, undisturbed, concentrically-zoned parent body, consistent with models that have been commonly invoked for H chondrites. Overlap of isochron ages for H4 and H5 chondrites, by contrast, appear to be more consistent with shallow impact disruption models. The W isotopic composition of metal from one CR chondrite was examined to compare with H chondrite metals. In contrast to the H chondrites, the CR chondrite metal is characterized by an enrichment in 183W that is consistent with nucleosynthetic s-process depletion. Once corrected for the correlative nucleosynthetic effect on 182W, the 182W model age for this meteorite of 7.0 ± 3.6 Ma is within the range of model ages of most metal fractions from H chondrites. The metal is therefore too young to be a direct nebular condensate, as proposed by some prior studies.

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.

High-precision analysis of 182W/184W and 183W/184W by negative thermal ionization mass spectrometry: Per-integration oxide corrections using measured 18O/16O.

Here we describe a new analytical technique for the high-precision measurement of 182W/184W and 183W/184W using negative thermal ionization mass spectrometry (N-TIMS). We improve on the recently reported method of Trinquier et al. (2016), which described using Faraday cup collectors coupled with amplifiers utilizing 1013 Ω resistors to continuously monitor the 18O/16O of WO3 - and make per-integration oxide corrections. In our study, we report and utilize a newly measured oxygen mass fractionation line, as well as average 17O/16O and 18O/16O, which allow for more accurate per-integration oxide interference corrections. We also report a Faraday cup and amplifier configuration that allows 18O/16O to be continuously monitored for WO3 - and ReO3 -, both of which are ionized during analyses of W using Re ribbon. The long-term external precision of 182W/184W is 5.7 ppm and 3.7 ppm (2SD) when mass bias corrected using 186W/184W and 186W/183W, respectively. For 183W/184W mass bias is corrected using 186W/184W, yielding a long-term external precision of 6.6 ppm. An observed, correlated variation in 182W/184W and 183W/184W, when mass bias corrected using 186W/184W, is most likely the result of Faraday cup degradation over months-long intervals.