A petrologic study of the IAB iron meteorites: Constraints on the formation of the IAB‐Winonaite parent body

Abstract— We studied 26 IAB iron meteorites containing silicate‐bearing inclusions to better constrain the many diverse hypotheses for the formation of this complex group. These meteorites contain inclusions that fall broadly into five types: (1) sulfide‐rich, composed primarily of troilite and containing abundant embedded silicates; (2) nonchondritic, silicate‐rich, comprised of basaltic, troctolitic, and peridotitic mineralogies; (3) angular, chondritic silicate‐rich, the most common type, with approximately chondritic mineralogy and most closely resembling the winonaites in composition and texture; (4) rounded, often graphite‐rich assemblages that sometimes contain silicates; and (5) phosphate‐bearing inclusions with phosphates generally found in contact with the metallic host. Similarities in mineralogy and mineral and O‐isotopic compositions suggest that IAB iron and winonaite meteorites are from the same parent body. We propose a hypothesis for the origin of IAB iron meteorites that combines some aspects of previous formation models for these meteorites. We suggest that the precursor parent body was chondritic, although unlike any known chondrite group. Metamorphism, partial melting, and incomplete differentiation (i.e., incomplete separation of melt from residue) produced metallic, sulfide‐rich and silicate partial melts (portions of which may have crystallized prior to the mixing event), as well as metamorphosed chondritic materials and residues. Catastrophic impact breakup and reassembly of the debris while near the peak temperature mixed materials from various depths into the re‐accreted parent body. Thus, molten metal from depth was mixed with near‐surface silicate rock, resulting in the formation of silicate‐rich IAB iron and winonaite meteorites. Results of smoothed particle hydrodynamic model calculations support the feasibility of such a mixing mechanism. Not all of the metal melt bodies were mixed with silicate materials during this impact and reaccretion event, and these are now represented by silicate‐free IAB iron meteorites. Ages of silicate inclusions and winonaites of 4.40‐4.54 Ga indicate this entire process occurred early in solar system history.     

The silicate inclusions of the Ocotillo IAB iron meteorite

Abstract— The Ocotillo IAB iron meteorite contains small silicate inclusions consisting of olivine, low-Ca pyroxene, chromian diopside, plagioclase, magnesiochromite, apatite, troilite and metal. The ferromagnesian silicates have a small range of Fe/(Fe + Mg) ratios that are not due to zoning. These phases appear to be not well equilibrated. The FeO content of magnesiochromite is lower than values normally seen in silicate assemblages in IAB iron meteorites. The minerals in Ocotillo are generally like silicate assemblages in other IAB meteorites, covering similar composition ranges and exhibiting a metamorphic (granoblastic) texture. An estimate was made of the bulk composition of Ocotillo silicate inclusions. The bulk composition is close to that of ordinary chondrites with the exception of a deficiency in CaO that might be due to a sampling problem associated with the method used to estimate the bulk composition.     

Portales Valley: Petrology of a metallic‐melt meteorite breccia

Abstract— Portales Valley (PV) is an unusual metal‐veined meteorite that has been classified as an H6 chondrite. It has been regarded either as an annealed impact melt breccia, as a primitive achondrite, or as a meteorite with affinities to silicated iron meteorites. We studied the petrology of PV using a variety of geochemical‐mineralogical techniques. Our results suggest that PV is the first well‐documented metallic‐melt meteorite breccia. Mineral‐chemical and other data suggest that the protolith to PV was an H chondrite. The composition of FeNi metal in PV is somewhat fractionated compared to H chondrites and varies between coarse vein and silicate‐rich portions. It is best modeled as having formed by partial melting at temperatures of ?940–1150 °C, with incomplete separation of solid from liquid metal. Solid metal concentrated in the coarse vein areas and S‐bearing liquid metal concentrated in the silicate‐rich areas, possibly as a result of a surface energy effect. Both carbon and phosphorus must have been scavenged from large volumes and concentrated in metallic liquid. Graphite nodules formed by crystallization from this liquid, whereas phosphate formed by reaction between P‐bearing metal and clinopyroxene components, depleting clinopyroxene throughout much of the meteorite and growing coarse phosphate at metal‐silicate interfaces. Some phosphate probably crystallized from P‐bearing liquids, but most probably formed by solid‐state reaction at ?975‐725 °C. Phosphate‐forming and FeO‐reduction reactions were widespread in PV and entailed a change in the mineralogy of the stony portion on a large scale. Portales Valley experienced protracted annealing from supersolidus to subsolidus temperatures, probably by cooling at depth within its parent body, but the main differences between PV and H chondrites arose because maximum temperatures were higher in PV. A combination of a relatively weak shock event and elevated pre‐shock temperatures probably produced the vein‐and‐breccia texture, with endogenic heating being the main heat source for melting, and with stress waves from an impact event being an essential trigger for mobilizing metal. Portales Valley is best classified as an H7 metallic‐melt breccia of shock stage S1. The meteorite is transitional between more primitive (chondritic) and evolved (achondrite, iron) meteorite types and offers clues as to how differentiation could have occurred in some asteroidal bodies.     

Restriction of parent body heating by metal‐troilite melting: Thermal models for the ordinary chondrites

Ordinary chondrite meteorites contain silicates, Fe,Ni‐metal grains, and troilite (FeS). Conjoined metal‐troilite grains would be the first phase to melt during radiogenic heating in the parent body, if temperatures reached over approximately 910–960 °C (the Fe,Ni‐FeS eutectic). On the basis of two‐pyroxene thermometry of 13 ordinary chondrites, we argue that peak temperatures in some type 6 chondrites exceeded the Fe,Ni‐FeS eutectic and thus conjoined metal‐troilite grains would have begun to melt. Melting reactions consume energy, so thermal models were constructed to investigate the effect of melting on the thermal history of the H, L, and LL parent asteroids. We constrained the models by finding the proportions of conjoined metal‐troilite grains in ordinary chondrites using high‐resolution X‐ray computed tomography. The models show that metal‐troilite melting causes thermal buffering and inhibits the onset of silicate melting. Compared with models that ignore the effect of melting, our models predict longer cooling histories for the asteroids and accretion times that are earlier by 61, 124, or 113 kyr for the H, L, and LL asteroids, respectively. Because the Ni/Fe ratio of the metal and the bulk troilite/metal ratio is higher in L and LL chondrites than H chondrites, thermal buffering has the greatest effect in models for the L and LL chondrite parent bodies, and least effect for the H chondrite parent. Metal‐troilite melting is also relevant to models of primitive achondrite parent bodies, particularly those that underwent only low degrees of silicate partial melting. Thermal models can predict proportions of petrologic types formed within an asteroid, but are systematically different from the statistics of meteorite collections. A sampling bias is interpreted to explain these differences.     

Zinc isotopic composition of iron meteorites: Absence of isotopic anomalies and origin of the volatile element depletion

High‐precision Zn isotopic compositions measured by MC‐ICP‐MS are documented for 32 iron meteorites from various fractionally crystallized and silicate‐bearing groups. The δ⁶⁶Zn values range from ?0.59‰ up to +5.61‰ with most samples being slightly enriched in the heavier isotopes compared with carbonaceous chondrites (0 < δ⁶⁶Zn < 0.5). The δ⁶⁶Zn versus δ⁶⁸Zn plot of all samples defines a common linear fractionation line, which supports the hypothesis that Zn was derived from a single reservoir or from multiple reservoirs linked by mass‐dependent fractionation processes. Our data for Redfields fall on a mass fractionation line and therefore refute a previous claim of it having an anomalous isotopic composition due to nonmixing of nucleosynthetic products. The negative correlation between δ⁶⁶Zn and the Zn concentration of IAB and IIE is consistent with mass‐dependent isotopic fractionation due to evaporation with preferential loss of lighter isotopes in the vapor phase. Data for the Zn concentrations and isotopic compositions of two IVA samples demonstrate that volatile depletion in the IVA parent body is not likely the result of evaporation. This is important evidence that favors the incomplete condensation origin for the volatile depletion of the IVA parent body.     

Silicon in iron meteorite metal

Abstract– We report Si concentrations in the metal phases of iron meteorites. Analyses were performed by secondary ion mass spectrometry using a CAMECA 1270 ion probe. The Si concentrations are low (0.09–0.46 μg g^?1), with no apparent difference in concentration between magmatic and nonmagmatic iron meteorites. Coexisting kamacite and Ni‐rich metal phases have similar Si contents. Thermodynamic calculations show that Fe,Ni‐metal in equilibrium with silicate melts at temperatures where metal crystallizes should contain approximately 100 times more Si than found in iron meteorites in this work. The missing Si may either occur as tiny silicate inclusions in metal or it may have diffused as Si‐metal into surrounding silicates at low temperatures. In both cases, extensive low‐temperature diffusion of Si in metal is required. It is therefore concluded that low Si in iron meteorites is a result of subsolidus reactions during slow cooling.     

The Antarctic achondrite,Grove Mountains 021663: An olivine‐rich winonaite

Abstract– The Grove Mountains (GRV) 021663 meteorite was collected from the Grove Mountains region of Antarctica. The meteorite is composed primarily of olivine (Fa_5.4), orthopyroxene (Fs_4.7Wo_3.0), chromian diopside (En_53.6Fs_2.4Wo₄₄), troilite, kamacite, and plagioclase (Ab_74.5Or₄An_21.5). Minor phases include schreibersite and K‐feldspar. The meteorite is highly weathered (W3) and weakly shocked (S2). We determine a whole rock oxygen isotopic composition of δ¹⁸O = 7.50‰, δ¹⁷O = 3.52‰. Comparisons of these data with other primitive achondrites have resulted in the reclassification of this meteorite as a member of the winonaite group. The occurrences of troilite, metal, and schreibersite in GRV 021663 indicate that these minerals were once completely molten. Euhedral inclusions of pyroxene within plagioclase further suggest that these may have crystallized from a silicate melt, while the depletion of plagioclase, metal, and troilite indicates that GRV 021663 could represent a residuum following partial melting on its parent asteroid. Trace element distributions in silicate minerals do not, however, confirm this scenario. As with other winonaite meteorites, the formation of GRV 021663 probably relates to brecciation and mixing of heterogeneous lithologies, followed by varying degrees of thermal metamorphism on the parent body asteroid. Peak metamorphic conditions may have resulted in localized partial melting of metal and silicate mineralogies, but our data are not conclusive.     

A new Martian meteorite from Oman: Mineralogy,petrology, and shock metamorphism of olivine‐phyric basaltic shergottite Sayh al Uhaymir 150

Abstract— The Sayh al Uhaymir (SaU) 150 meteorite was found on a gravel plateau, 43.3 km south of Ghaba, Oman, on October 8, 2002. Oxygen isotope (δ¹⁷O 2.78; δ¹⁸O 4.74), CRE age (?1.3 Ma), and noble gas studies confirm its Martian origin. SaU 150 is classified as an olivine‐phyric basalt, having a porphyritic texture with olivine macrocrysts set in a finer‐grained matrix of pigeonite and interstitial maskelynite, with minor augite, spinel, ilmenite, merrillite, pyrrhotite, pentlandite, and secondary (terrestrial) calcite and iron oxides. The bulk rock composition, in particular mg (68) [molar Mg/(Mg + Fe) x 100], Fe/Mn (37.9), and Na/Al (0.22), are characteristic of Martian meteorites. Based on mineral compositions, cooling rates determined from crystal morphology, and crystal size distribution, it is deduced that the parent magma formed in a steady‐state growth regime (magma chamber) that cooled at <°C/hr. Subsequent eruption as a thick lava flow or hypabyssal intrusion entrained a small fraction of xenocrystic olivine and gave rise to a magmatic foliation, with slow cooling allowing for near homogenization of igneous minerals. SaU 150 experienced an equilibration shock pressure of 33–45 GPa in a single impact event. Post‐shock heat gave rise to localized melting (?11 vol%). Larger volume melts remained fluid after pressure release and crystallized dendritic olivine and pyroxene with fractal dimensions of 1.80–1.89 and 1.89–1.95, respectively, at ‐ΔT >70–365 °C. SaU 150 is essentially identical to SaU 005/094, all representing samples of the same fall that are similar to, but distinct from, the DaG shergottites.     

Watson: A new link in the HE iron chain

Abstract— Watson, which was found in 1972 in South Australia, contains the largest single silicate rock mass seen in any known iron meteorite. A comprehensive study has been completed on this unusual meteorite: petrography, metallography, analyses of the silicate inclusion (whole rock chemical analysis, INAA, RNAA, noble gases, and oxygen isotope analysis) and mineral compositions (by electron microprobe and ion microprobe). The whole rock has a composition of an H-chondrite minus the normal H-group metal and troilite content. The oxygen isotope composition is that of the silicates in the HE iron meteorites and lies along an oxygen isotope fractionation line with the H-group chondrites. Trace elements in the metal confirm Watson is a new HE iron. Whole rock Watson silicate shows an enrichment in K and P (each ～2X H-chondrites). The silicate inclusion has a highly equilibrated igneous (peridotite-like) texture with olivine largely poikilitic within low-Ca pyroxene: olivine (Fa₂₀), opx (Fs₁₇Wo₃), capx (Fs₉Wo₄₁) (with very fine exsolution lamellae), antiperthite feldspar (An_1–Or₅) with <1 μm exsolution lamellae (An_1–3Or_>40), shocked feldspar with altered stoichiometry, minor whitlockite (also a poorly characterized interstitial phosphate-rich phase) and chromite, and only traces of metal and troilite. The individual silicate minerals have normal chondritic REE patterns, but whitlockite has a remarkable REE pattern. It is very enriched in light REE (La is 720X C1, and Lu is 90X C1, as opposed to usual chonditic values of ～300X and 100–150X, respectively) with a negative Eu anomaly. The enrichment of whole rock K is expressed both in an unusually high mean modal Or content of the feldspar, Or₁₃, and in the presence of antiperthite. Whole rock trace element data for the silicate mass support the petrography. Watson silicate was an H-chondrite engulfed by metal and melted at > 1550 °C. A flat refractory lithophile and flat REE pattern (at ～1x average H-chondrites) indicate that melting took place in a relatively closed system. Immiscible metal and sulfide were occluded into the surrounding metal host. Below 1100 °C, the average cooling rate is estimated to have been ～1000 °C/Ma; Widmanstätten structure formed, any igneous zoning in the silicates was equilibrated, and feldspar and pyroxene exsolution took place. Cooling to below 300 °C was completed by 3.5 Ga B. P. At 8 Ma, a shock event took place causing some severe metal deformation and forming local melt pockets of schreibersite/metal. This event likely caused the release of Watson into interplanetary space. The time of this event, 8Ma, corresponds to the peak frequency of exposure ages of the H-chondrites. This further confirms the link between HE irons and the H-chondrites, a relationship already indicated by their common oxygen isotope source. Watson metal structures are very similar to those in Kodaikanal. Watson, Kodaikanal and Netschaëvo form the young group of HE meteorites (ages 3.7 ± 0.2 Ga). They appear to represent steps in a chain of events that must have taken place repeatedly on the HE parent body or bodies from which they came: chondrite engulfed in metal (Netschaëvo); chondrite melted within metal (Watson); and finally melted silicate undergoing strong fractionation with the fractionated material emplaced as globules within metal (Kodaikanal). Watson fills an important gap in understanding the sequence of events that took place in the evolution of the IIE-H parent body(ies). This association of H-chondrite with HE metal suggests a surface, or near surface process-a suggestion made by several other researchers.     

A review of the chondrite–achondrite transition,and a metamorphic facies series for equilibrated primitive stony meteorites

Here, the petrological features of numerous primitive achondrites and highly equilibrated chondrites are evaluated to review and expand upon our knowledge of the chondrite–achondrite transition, and primitive achondrites in general. A thermodynamic model for the initial silicate melting temperature and progressive melting for nearly the entire known range of oxidation states is provided, which can be expressed as T_m = 0.035Fa²?3.51Fa + 1109 (in °C, where Fa is the proportion of fayalite in olivine). This model is then used to frame a discussion of textural and mineralogical evolution of stony meteorites with increasing temperature. We suggest that the metamorphic petrology of these meteorites should be based on diffusive equilibration among the silicate minerals, and as such, the chondrite–achondrite transition should be defined by the initial point of silicate melting, not by metal–troilite melting. Evidence of silicate melting is preserved by a distinctive texture of interconnected interstitial plagioclase ± pyroxene networks among rounded olivine and/or pyroxene (depending on ?O₂), which pseudomorph the former silicate melt network. Indirectly, the presence of exsolution lamellae in augite in slowly cooled achondrites also implies that silicate melting occurred because of the high temperatures required, and because silicate melt enhances diffusion. A metamorphic facies series is defined: the Plagioclase Facies is equivalent to petrologic types 5 and 6, the Sub‐calcic Augite Facies is bounded at lower temperatures by the initiation of silicate melting and at higher temperatures by the appearance of pigeonite, which marks the transition to the Pigeonite Facies.     

Genesis of the IIICD iron meteorites: Evidence from silicate-bearing inclusions

Abstract— Our studies of the silicate-bearing inclusions in the IIICD iron meteorites Maltahöhe, Carlton and Dayton suggest that their mineralogy and mineral compositions are related to the composition of the metal in the host meteorites. An inclusion in the low-Ni Maltahöhe is similar in mineralogy to those in IAB irons, which contain olivine, pyroxene, plagioclase, graphite and troilite. With increasing Ni concentration of the metal, silicate inclusions become poorer in graphite, richer in phosphates, and the phosphate and silicate assemblages become more complex. Dayton contains pyroxene, plagioclase, SiO₂, brianite, panethite and whitlockite, without graphite. In addition, mafic silicates become more FeO-rich with increasing Ni concentration of the hosts. In contrast, silicates in IAB irons show no such correlation with host Ni concentration, nor do they have the complex mineral assemblages of Dayton. These trends in inclusion composition and mineralogy in IIICD iron meteorites have been established by reactions between the S-rich metallic magma and the silicates, but the physical setting is uncertain. Of the two processes invoked by other authors to account for groups IAB and IIICD, fractional crystallization of S-rich cores and impact generation of melt pools, we prefer core crystallization. However, the absence of relationships between silicate inclusion mineralogy and metal compositions among IAB irons analogous to those that we have discovered in IIICD irons suggests that the IAB and IIICD cores/metallic magmas evolved in rather different ways. We suggest that the solidification of the IIICD core may have been very complex, involving fractional crystallization, nucleation effects and, possibly, liquid immiscibility.     

Petrology of silicate inclusions in the Sombrerete ungrouped iron meteorite: Implications for the origins of IIE‐type silicate‐bearing irons

Abstract— The petrography and mineral and bulk chemistries of silicate inclusions in Sombrerete, an ungrouped iron that is one of the most phosphate‐rich meteorites known, was studied using optical, scanning electron microscopy (SEM), electron microprobe analysis (EMPA), and secondary ion mass spectrometry (SIMS) techniques. Inclusions contain variable proportions of alkalic siliceous glass (?69 vol% of inclusions on average), aluminous orthopyroxene (?9%, Wo_1–4Fs_25–35, up to ?3 wt% Al), plagioclase (?8%, mainly An_70–92), Cl‐apatite (?7%), chromite (?4%), yagiite (?1%), phosphate‐rich segregations (?1%), ilmenite, and merrillite. Ytterbium and Sm anomalies are sometimes present in various phases (positive anomalies for phosphates, negative for glass and orthopyroxene), which possibly reflect phosphate‐melt‐gas partitioning under transient, reducing conditions at high temperatures. Phosphate‐rich segregations and different alkalic glasses (K‐rich and Na‐rich) formed by two types of liquid immiscibility. Yagiite, a K‐Mg silicate previously found in the Colomera (IIE) iron, appears to have formed as a late‐stage crystallization product, possibly aided by Na‐K liquid unmixing. Trace‐element phase compositions reflect fractional crystallization of a single liquid composition that originated by low‐degree (?4–8%) equilibrium partial melting of a chondritic precursor. Compositional differences between inclusions appear to have originated as a result of a “filter‐press differentiation” process, in which liquidus crystals of Cl‐apatite and orthopyroxene were less able than silicate melt to flow through the metallic host between inclusions. This process enabled a phosphoran basaltic andesite precursor liquid to differentiate within the metallic host, yielding a dacite composition for some inclusions. Solidification was relatively rapid, but not so fast as to prevent flow and immiscibility phenomena. Sombrerete originated near a cooling surface in the parent body during rapid, probably impact‐induced, mixing of metallic and silicate liquids. We suggest that Sombrerete formed when a planetesimal undergoing endogenic differentiation was collisionally disrupted, possibly in a breakup and reassembly event. Simultaneous endogenic heating and impact processes may have widely affected silicate‐bearing irons and other solar system matter.     

Accretion of differentiated achondritic and aqueously altered chondritic materials in the early solar system—Significance of an igneous fragment in the CM chondrite NWA 12651

One approach to decipher the dynamics of material transport and planetary accretion in the early solar system is to investigate xenolithic fragments in meteorites. In this work, we examined an igneous fragment from the NWA 12651 meteorite—the first igneous fragment found in any CM chondrite—by analyzing its mineralogy, rare earth elements (REEs), and O‐isotopes. The study shows that the exsolution lamellae of the igneous fragment consist of Fe‐rich and Ca‐rich pyroxene. Thus, the fragment was part of a progressive crystallization in a closed system, such as in a depleted magma reservoir or mantle. In this environment, the pyroxene co‐crystallized with plagioclase, resulting in a negative Eu anomaly and enrichment of the heavy REEs compared to the light REEs. The O‐isotopes of the fragment are more ¹⁶O‐enriched than the mafic minerals in the matrix or in other bulk CM chondrites; therefore, the fragment was formed in a different region than the NWA 12651 parent body. The iron meteorites Tucson and Deep Springs, the pallasite Milton, and the CB chondrites have similar O‐isotopes as the igneous fragment. However, no direct connection can be drawn and it is questionable if the fragment shares a same parent body with one of these meteorites. The close formation region to the CB chondrites may suggest a formation of the fragment in the carbonaceous chondrite region. Thus, a wide transport through the nebula of the early solar system may not have been necessary to move the fragment to the CM chondrite formation region.     

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.     

Spectral properties and mineral compositions of acapulcoite–lodranite clan meteorites: Establishing S‐type asteroid–meteorite connections

Except for asteroid sample return missions, measurements of the spectral properties of both meteorites and asteroids offer the best possibility of linking meteorite groups with their parent asteroid(s). Visible plus near‐infrared spectra reveal distinguishing absorption features controlled mainly by the Fe²⁺ contents and modal abundances of olivine and pyroxene. Meteorite samples provide relationships between spectra and mineralogy. These relationships are useful for estimating the olivine and pyroxene mineralogy of stony (S‐type) asteroid surfaces. Using a suite of 10 samples of the acapulcoite–lodranite clan (ALC), we have developed new correlations between spectral parameters and mafic mineral compositions for partially melted asteroids. A well‐defined relationship exists between Band II center and ferrosilite (Fs) content of orthopyroxene. Furthermore, because Fs in orthopyroxene and fayalite (Fa) content in olivine are well correlated in these meteorites, the derived Fs content can be used to estimate Fa of the coexisting olivine. We derive new equations for determining the mafic silicate compositions of partially melted S‐type asteroid parent bodies. Stony meteorite spectra have previously been used to delineate meteorite analog spectral zones in Band I versus band area ratio (BAR) parameter space for the establishment of asteroid–meteorite connections with S‐type asteroids. However, the spectral parameters of the partially melted ALC overlap with those of ordinary (H) chondrites in this parameter space. We find that Band I versus Band II center parameter space reveals a clear distinction between the ALC and the H chondrites. This work allows the distinction of S‐type asteroids as nebular (ordinary chondrites) or geologically processed (primitive achondrites).     

Reclassification of four aubrites as enstatite chondrite impact melts: Potential geochemical analogs for Mercury

We present petrologic and isotopic data on Northwest Africa (NWA) 4799, NWA 7809, NWA 7214, and NWA 11071 meteorites, which were previously classified as aubrites. These four meteorites contain between 31 and 56 vol% of equigranular, nearly endmember enstatite, Fe,Ni metal, plagioclase, terrestrial alteration products, and sulfides, such as troilite, niningerite, daubréelite, oldhamite, and caswellsilverite. The equigranular texture of the enstatite and the presence of the metal surrounding enstatite indicate that these rocks were not formed through igneous processes like the aubrites, but rather by impact processes. In addition, the presence of pre‐terrestrially weathered metal (7.1–14 vol%), undifferentiated modal abundances compared to enstatite chondrites, presence of graphite, absence of diopside and forsterite, low Ti in troilite, and high Si in Fe,Ni metals suggest that these rocks formed through impact melting on chondritic and not aubritic parent bodies. Formation of these meteorites on a parent body with similar properties to the EHa enstatite chondrite parent body is suggested by their mineralogy. These parent bodies have undergone impact events from at least 4.5 Ga (NWA 11071) until at least 4.2 Ga (NWA 4799) according to ³⁹Ar‐⁴⁰Ar ages, indicating that this region of the solar system was heavily bombarded early in its history. By comparing NWA enstatite chondrite impact melts to Mercury, we infer that they represent imperfect petrological analogs to this planet given their high metal abundances, but they could represent important geochemical analogs for the behavior and geochemical affinities of elements on Mercury. Furthermore, the enstatite chondrite impact melts represent an important petrological analog for understanding high‐temperature processes and impact processes on Mercury, due to their similar mineralogies, Fe‐metal‐rich and FeO‐poor silicate abundances, and low oxygen fugacity.     

Sulfide‐rich metallic impact melts from chondritic parent bodies

Abstract– Sacramento Wash 005 (SaW) 005, Meteorite Hills 00428 (MET) 00428, and Mount Howe 88403 (HOW) 88403 are S‐rich Fe,Ni‐rich metal meteorites with fine metal structures and homogeneous troilite. We compare them with the H‐metal meteorite, Lewis Cliff 88432. Phase diagram analyses suggest that SaW 005, MET 00428, and HOW 88403 were liquids at temperatures above 1350 °C. Tridymite in HOW 88403 constrains formation to a high‐temperature and low‐pressure environment. The morphology of their metal‐troilite structures may suggest that MET 00428 cooled the slowest, SaW 005 cooled faster, and HOW 88403 cooled the quickest. SaW 005 and MET 00428 contain H‐chondrite like silicates, and SaW 005 contains a chondrule‐bearing inclusion that is texturally and compositionally similar to H4 chondrites. The compositional and morphological similarities of SaW 005 and MET 00428 suggest that they are likely the result of impact processing on the H‐chondrite parent body. SaW 005 and MET 00428 are the first recognized iron‐ and sulfide‐rich meteorites, which formed by impact on the H‐chondrite parent body, which are distinct from the IIE‐iron meteorite group. The morphological and chemical differences of HOW 88403 suggest that it is not from the H‐chondrite body, although it likely formed during an impact on a chondritic parent body.     

Two distinct assemblages of high‐pressure liquidus phases in shock veins of the Sixiangkou meteorite

Abstract— Shock‐produced complex veins, including earlier and later veins, are identified in the Sixiangkou L6 chondrite. The early vein is intersected by the late vein and consists of coarse‐grained aggregates of ringwoodite, majorite, and lingunite, and fragments of olivine, pyroxene, plagioclase, metal, and troilite, as well as a fine‐grained matrix of garnet, ringwoodite, metal, and troilite. The late vein mainly consists of a fine‐grained matrix of garnet, magnesiowüstite, metal, and troilite, as well as a small amount of coarse‐grained aggregates. The amount of fine‐grained matrix suggests that the late vein was nearly completely melted, whereas the early vein underwent partial melting. Both fine‐grained assemblages of garnet plus ringwoodite in the early vein and garnet plus magnesiowüstite in the late vein are liquidus phases crystallized from shock‐induced melt. Based on our understanding of the liquidus assemblages, the late vein experienced a higher pressure and temperature than the early vein.