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.     

Chemical and genetic characterization of the ungrouped pallasite Lieksa

The meteorite Lieksa was found in 2017 in Löpönvaara, Finland, and later donated to the Finnish Museum of Natural History. Here, we report siderophile element concentrations, genetic isotopic data, and a metal–silicate segregation age for the meteorite. The ~280 g Lieksa is ~80% metal and ~20% silicate and oxide inclusions by volume, with the inclusions consisting primarily of Fe-rich olivine. Due to Lieksa's silicate content, coupled with a texture characterized by metal enclosing the silicates, it has been classified as a pallasite. Lieksa's olivine and bulk chemical characteristics are distinct from those of the known pallasite and iron meteorite groups, consistent with its classification as ungrouped. The meteorite exhibits a flat, chondrite-normalized highly siderophile element pattern, consistent with an origin as an early crystallization product from a metallic melt with chondritic relative abundances. Molybdenum, Ru, and ¹⁸³W isotopic data indicate that Lieksa formed in the non-carbonaceous (NC) domain of the solar nebula. Radiogenic ¹⁸²W abundances for Lieksa yield a model metal–silicate segregation age of 1.5 ± 0.8 Myr after calcium-aluminum-rich inclusion formation, which is within the range established for other NC-type pallasite and iron meteorite parent bodies.     

Olivine zoning and retrograde olivine‐orthopyroxene‐metal equilibration in H5 and H6 chondrites

Abstract— Electron microprobe studies of several H5 and H6 chondrites reveal that olivine crystals exhibit systematic Fe‐Mg zoning near olivine‐metal interfaces. Olivine Fa concentrations decrease by up to 2 mol% toward zoned taenite + kamacite particles (formed after relatively small amounts of taenite undercooling) and increase by up to 2 mol% toward zoneless plessite particles (formed after ?200 °C of taenite undercooling). The olivine zoning can be understood in terms of localized olivine‐orthopyroxene‐metal reactions during cooling from the peak metamorphic temperature. The silicate‐metal reactions were influenced by solid‐state metal phase transformations, and the two types of olivine zoning profiles resulted from variable amounts of taenite undercooling at temperatures <700 °C. The relevant silicate‐metal reactions are modeled using chemical thermodynamics. Systematic olivine Fe‐Mg zoning adjacent to metal is an expected consequence of retrograde silicate‐metal reactions, and the presence of such zoning provides strong evidence that the silicate and metallic minerals evolved in situ during cooling from the peak metamorphic temperature.     

Petrology and geochemistry of a silicate clast from the Mount Padbury mesosiderite: Implications for metal‐silicate mixing events of mesosiderite

Abstract— Petrological and bulk geochemical studies were performed on a large silicate clast from the Mount Padbury mesosiderite. The silicate clast is composed mainly of pyroxene and plagioclase with minor amounts of ilmenite, spinel, and other accessory minerals, and it shows subophitic texture. Pyroxenes in the clast are similar to those in type 5 eucrites and could have experienced prolonged thermal metamorphism after rapid crystallization from a near‐surface melt. Ilmenite and spinel vary chemically, indicating growth under disequilibrium conditions. The clast seems to have experienced an episode of rapid reheating and cooling, possibly as a result of metal‐silicate mixing. Abundances of siderophile elements are obviously higher than in eucrites, although the clast is also extremely depleted in highly siderophile elements. The fractionated pattern can be explained by injection of Fe‐FeS melts generated by partial melting of metallic portions during metal‐silicate mixing. The silicate clast had a complex petrogenesis that could have included: 1) rapid crystallization from magma in a lava flow or a shallow intrusion; 2) prolonged thermal metamorphism to equilibrate the mineral compositions of pyroxene and plagioclase after primary crystallization; 3) metal‐silicate mixing probably caused by the impact of solid metal bodies on the surface of the mesosiderite parent body; and 4) partial melting of metal and sulfide portions (and silicate in some cases) caused by the collisional heating, which produced Fe‐FeS melts with highly fractionated siderophile elements that were injected into silicate portions along cracks and fractures.     

Crystallization of magmatic iron meteorites: The effects of phosphorus and liquid immiscibility

Abstract— Magmatic iron meteorites are commonly thought to have formed by fractional crystallization of the metallic cores of asteroid‐sized bodies. As fractional crystallization proceeds, light elements such as P and S become enriched in the molten portion of the core. The light element content of the metallic liquid influences the partitioning behavior of trace elements and may cause liquid immiscibility to occur. The elemental trends observed in magmatic iron meteorites may have been affected by both of these processes. We have examined experimentally the effect of P on the solid‐metal‐liquid‐metal partitioning behavior of Ag and Pd, Re and Os, two element pairs used to date iron meteorite processes. Phosphorus has no effect on the partition coefficient of either Ag or Pd, which are incompatible and identical within experimental error. Compatible Re and Os also have identical partitioning behavior, within experimental error, and show increasing compatibility in the solid metal with increasing P content of the metallic liquid. Including the effects of both S and P on the partitioning behavior of Re and Os, simple fractional crystallization calculations can reproduce the large variation of Re and Os concentrations observed in four magmatic iron meteorite groups but have difficulty matching the later crystallizing portions of the trends. We have also conducted experiments with three phases—solid metal and two immiscible metallic liquids—to determine the location of the liquid immiscibility field near conditions thought to be relevant to magmatic iron meteorites. Our results show a significantly smaller liquid immiscibility field as compared to the previously published Fe‐P‐S phase diagram. Our revised phase diagram suggests that liquid immiscibility was encountered during the crystallization of asteroidal cores, but much later during the crystallization process than predicted by the previously published diagram.     

Petrology of the Asuka 881931 ureilite with special reference to crystallization of interstitial silicate melt

Abstract— The Asuka 881931 meteorite is an unbrecciated ferroan ureilite and consists mainly of equi—granular olivine and pigeonite grains, a metal—sulfide network, interstitial silicates, and glass. Peripheral portions of equigranular olivine grains are often replaced by fine-grained forsterite—metal aggregates and sometimes by fine-grained enstatite—metal aggregates. These aggregates may have been produced from the equigranular olivine by reduction. Peripheral portions of equigranular pigeonite grains also are sometimes replaced by fine-grained orthopyroxene aggregates with tiny patches of Si-rich glass and may have been produced from the pigeonite by reduction reaction with silicate melt. Interstitial silicates are mainly orthopyroxene, magnesian pigeonite, high-Ca pyroxene (diopside/fassaite), and CaO-poor enstatite; and they crystallized from interstitial silicate melt. Interstitial glass is classified into two types—-Si-poor and Si-rich. The Si-poor glass is always in contact with equigranular olivine, but the Si-rich glass never contacts equigranular olivine and is in contact with pyroxene and the metal—sulfide network. Both types of glass were produced from an original interstitial silicate melt, but the Si-poor glass formed mainly by fractional crystallization of pyroxenes, and the Si-rich glass may have formed by addition of Si mainly from nearby metal—sulfide melt, as well as crystallization of pyroxenes. The Si-poor and Si-rich melts were finally quenched as interstitial glasses under rapid cooling conditions.     

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.     

Highly siderophile element (HSE) abundances in the mantle of Mars are due to core formation at high pressure and temperature

Highly siderophile elements (HSEs) can be used to understand accretion and core formation in differentiated bodies, due to their strong affinity for FeNi metal and sulfides. Coupling experimental studies of metal–silicate partitioning with analyses of HSE contents of Martian meteorites can thus offer important constraints on the early history of Mars. Here, we report new metal–silicate partitioning data for the PGEs and Au and Re across a wide range of pressure and temperature space, with three series designed to complement existing experimental data sets for HSE. The first series examines temperature effects for D(HSE) in two metallic liquid compositions—C‐bearing and C‐free. The second series examines temperature effects for D(Re) in FeO‐bearing silicate melts and FeNi‐rich alloys. The third series presents the first systematic study of high pressure and temperature effects for D(Au). We then combine our data with previously published partitioning data to derive predictive expressions for metal–silicate partitioning of the HSE, which are subsequently used to calculate HSE concentrations of the Martian mantle during continuous accretion of Mars. Our results show that at midmantle depths in an early magma ocean (equivalent to approximately 14 GPa, 2100 °C), the HSE contents of the silicate fraction are similar to those observed in the Martian meteorite suite. This is in concert with previous studies on moderately siderophile elements. We then consider model calculations that examine the role of melting, fractional crystallization, and sulfide saturation/undersaturation in establishing the range of HSE contents in Martian meteorites derived from melting of the postcore formation mantle. The core formation modeling indicates that the HSE contents can be established by metal–silicate equilibrium early in the history of Mars, thus obviating the need for a late veneer for HSE, and by extension volatile siderophile elements, or volatiles in general.     

A study of the minor element concentrations of spinels from two type B calcium-aluminum-rich inclusions: An investigation into potential formation conditions of calcium-aluminum-rich inclusions

Abstract— We have conducted an electron microprobe study of minor element distributions among spinels from two type B1 calcium-aluminum-rich inclusions (CAIs): Allende TS-23 and Leoville 3537–2. We show that by maintaining the petrologic context (edge, middle, and center of the inclusion plus their host silicate phase), four populations of spinels are resolvable based on their minor element contents. One population resides within the edge area (mainly mantle melilite) and is characterized by the highest V contents. Unlike Leoville 3537–2, many edge grains from Allende TS-23 also have high-Fe contents (up to 4.0 wt%) and low-Cr values. Based on their V and Ti concentrations (which is positively correlated), middle and center grains define a trend that is divided into three populations: spinels enclosed by melilite, fassaite, and anorthite. The overall range in Ti concentration based on fractional crystallization should be much less than a factor of 2; however, the observed range is considerably larger. The minor element contents of these grains are interpreted as recording alteration, primary fractional crystallization, and a complex igneous history that may involve remelting and recrystallization. From our data, Allende TS-23 has experienced more alteration than Leoville 3537–2, which is consistent with previous petrologic studies of silicates within these objects; yet both objects have likely been remelted (at least one additional melting event, possibly two, postdating the initial formation of these CAIs). By invoking a remelting history, the large range ir Ti concentrations and the different populations of spinels can be explained. Although our data suggest that more than one generation of spinels exist within these objects, we are unable to establish any population of relic spinel grains that predate the initial melting event.     

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.     

The most primitive mesosiderite Northwest Africa 1878, subgroup 0

All mesosiderites previously reported were subjected to thermal metamorphism and/or partial melting on the parent body. Therefore, their primordial features have been mostly lost. Here, we report detailed petrological and mineralogical features on a mesosiderite, Northwest Africa (NWA) 1878. This meteorite comprises silicate lithology and aggregates of small spheroidal Fe‐Ni metal grains. Silicate lithology typically shows igneous texture without recrystallization features, and mainly consists of low‐Ca pyroxene and plagioclase. Pyroxenes often show normal zoning. Exsolution lamella of augite is rarely noticed and very thin in width, compared with other mesosiderites. A few magnesian olivine grains are encountered without typical corona texture around them. They are not equilibrated with pyroxene on a large scale. Plagioclase shows a wide compositional range. These results show that NWA 1878 hardly experienced thermal metamorphism, distinguished from mesosiderites of subgroups 1–4. Therefore, we propose that this is classified as subgroup 0 mesosiderite. Nevertheless, NWA 1878 was locally subjected to secondary reactions, such as weak reduction of pyroxene and Fe‐Mg diffusion between olivine and pyroxene, on the parent body.     

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.     

An analytical electron microscopy (AEM) investigation of opaque inclusions in some type 6 ordinary chondrites

Abstract— A large number of ordinary chondrites contains micron-sized particles of metal and/or troilite dispersed in their silicate grains. Such metallic phases are responsible for the so-called darkening of the silicate grains and might be either precipitates, which formed during reduction of the silicates, or inclusions injected as a melt during a shock event. We have investigated these tiny foreign phases by analytical transmission electron microscopy in three unweathered, metamorphosed ordinary chondrites (Saint Séverin, LL6, Tsarev, L6 and Kernouvé, H6). We also looked for remnant shock indices. Our TEM observations suggest the following sequence of events in the three meteorites. First, a number of relatively strong shock events occurred on the parent body/bodies producing an Fe-FeS melt that was injected into silicate grains along a dense network of open fractures. Most of these shock defects were subsequently erased by high-temperature (700–900 °C) thermal metamorphism. Some remnants of the shock events are the observed trails of tiny metal and/or sulfide inclusions that formed as a result of fracture healing. Chemical homogenization of the silicates and limited oxidation of the metallic blebs also occurred during this high-temperature annealing event, resulting in Ni-rich inclusions. This effect was especially pronounced in the L and LL-chondrites studied. During subsequent cooling of the body/bodies, inclusions of chromite and phosphate precipitated, nucleating preferentially on lattice defects (dislocations, subgrain boundaries) and on the metal and sulfide inclusions. A later shock event of moderate intensity, probably corresponding to the separation of the meteorite from its parent body, produced new shock features in the silicate grains of the Saint Séverin meteorite, including mechanical twins in diopside and straight free screw dislocations in olivine.     

Crystallization of magmatic iron meteorites: The role of mixing in the molten core

Abstract— The IIIAB group is the largest of the magmatic iron meteorite groups and consequently is commonly used to test models of asteroid core crystallization. Simple fractional crystallization calculations appear to reproduce the general shape of the elemental trends observed in the IIIAB group when these trends are plotted vs. Ni, as is traditionally done. However, when the elemental trends are examined vs. another element (such as Ge vs. Ir), simple fractional crystallization fails to match a significant portion of the trend, specifically meteorites formed during the final stages of crystallization. Our simple mixing model, which attempts to account for the possibility of inhomogeneities in the molten metallic core, is able to reproduce the entire IIIAB trend observed. This model is a variant of simple fractional crystallization and involves mixing between a zone of liquid involved in the crystallization process and a second zone too far from the crystallizing solid to be actively involved in crystallization. This model does not suggest one unique solution for the method by which an asteroidal core crystallizes; rather it demonstrates that including the effects of mixing in the molten core can account for the observed IIIAB elemental trends, particularly the late-stage crystallizing members, which other models have difficulty explaining.     

Differentiation and evolution of the IVA meteorite parent body: Clues from pyroxene geochemistry in the Steinbach stony‐iron meteorite

Abstract— We analyzed the Steinbach IVA stony‐iron meteorite using scanning electron microscopy (SEM), electron microprobe analysis (EMPA), laser ablation inductively‐coupled‐plasma mass spectroscopy (LA‐ICP‐MS), and modeling techniques. Different and sometimes adjacent low‐Ca pyroxene grains have distinct compositions and evidently crystallized at different stages in a chemically evolving system prior to the solidification of metal and troilite. Early crystallizing pyroxene shows evidence for disequilibrium and formation under conditions of rapid cooling, producing clinobronzite and type 1 pyroxene rich in troilite and other inclusions. Subsequently, type 2 pyroxene crystallized over an extensive fractionation interval. Steinbach probably formed as a cumulate produced by extensive crystal fractionation (?60–70% fractional crystallization) from a high‐temperature (?1450–1490 °C) silicate‐metallic magma. The inferred composition of the precursor magma is best modeled as having formed by ≥30–50% silicate partial melting of a chondritic protolith. If this protolith was similar to an LL chondrite (as implied by O‐isotopic data), then olivine must have separated from the partial melt, and a substantial amount (?53–56%) of FeO must have been reduced in the silicate magma. A model of simultaneous endogenic heating and collisional disruption appears best able to explain the data for Steinbach and other IVA meteorites. Impact disruption occurred while the parent body was substantially molten, causing liquids to separate from solids and oxygen‐bearing gas to vent to space, leading to a molten metal‐rich body that was smaller than the original parent body and that solidified from the outside in. This model can simultaneously explain the characteristics of both stony‐iron and iron IVA meteorites, including the apparent correlation between metal composition and metallographic cooling rate observed for metal.     

Contribution of early impact events to metal‐silicate separation,thermal annealing,and volatile redistribution: Evidence in the Pułtusk H chondrite

Three‐dimensional X‐ray tomographic reconstructions and petrologic studies reveal voluminous accumulations of metal in Pu?tusk H chondrite. At the contact of these accumulations, the chondritic rock is enriched in troilite. The rock contains plagioclase‐rich bands, with textures suggesting crystallization from melt. Unusually large phosphates are associated with the plagioclase and consist of assemblages of merrillite, and fluorapatite and chlorapatite. The metal accumulations were formed by impact melting, rapid segregation of metal‐sulfide melt and the incorporation of this melt into the fractured crater basement. The impact most likely occurred in the early evolution of the H chondrite parent body, when post‐impact heat overlapped with radiogenic heat. This enabled slow cooling and separation of the metallic melt into metal‐rich and sulfide‐rich fractions. This led to recrystallization of chondritic rock in contact with the metal accumulations and the crystallization of shock melts. Phosphorus was liberated from the metal and subsumed by the silicate shock melt, owing to oxidative conditions upon slow cooling. The melt was also a host for volatiles. Upon further cooling, phosphorus reacted with silicates leading to the formation of merrillite, while volatiles partitioned into the residual halogen‐rich, dry fluid. In the late stages, the fluid altered merrillite to patchy Cl/F‐apatite. The above sequence of alterations demonstrates that impact during the early evolution of chondritic parent bodies might have contributed to local metal segregation and silicate melting. In addition, postshock conditions supported secondary processes: compositional/textural equilibration, redistribution of volatiles, and fluid alterations.     

THE Mg-Cr RELATIONSHIP IN ACHONDRITES AND IN THE SILICATE FRACTION OF MESOSIDERITES,AND ADDITIONAL OBSERVATIONS ON EUCRITES

New data are used to confirm the positive correlation between Mg and Cr in howardites and eucrites, and the identity of the Mg/Cr ratio in the two meteorite groups is established, provided Chaves is treated as an anomalous howardite. Macibini, usually classed as a eucrite, has higher contents of Mg and Cr than all but the cumulate eucrites; the suggestion is made, on the basis of its polymict character, the wide compositional range of its constituent clasts, and its bulk chemistry, that it should be re-classified as a howardite. The Mg-Cr relationship in diogenites is one of almost constant Mg but extremely variable Cr. The “average diogenite” plots fairly close to the trend established for the howardites and eucrites, indicative of the genetic link between these three meteorite classes. The silicate fractions of nine mesosiderites studied do not show a close coherence of Mg and Cr. With the exception of Patwar, they contain more Cr than howardites and eucrites, and exhibit greater variation of Cr relative to Mg. The general lack of clear inter-element trends in these silicate fractions suggests that they had a more complex origin and evolution than the silicates of the achondrites. Preliminary results of quantitative computer modeling of major and trace elements in the eucrites indicate that about 32 percent fractional crystallization of a eucritic liquid of the composition of Sioux County yields a residual liquid similar to Nuevo Laredo; the cumulate produced has the approximate composition of the cumulate eucrite Moama. These results are in agreement with the model developed by Consolmagno and Drake (1977), using the rare earth elements, for a corresponding stage in the solidification of an initial eucritic liquid produced by equilibrium partial melting of the source region of the parent body (Stolper, 1977). Plotting of the Ti concentrations of the meteorites studied against their Fe/Fe+Mg ratios supports Stolper's idea that the eucrites and the Mg-rich achondrites do not lie on the same liquid line of descent, and shows that the mesosiderite silicates do not conform to either trend.     

Evidence for fractional condensation and reprocessing at high temperatures in CH chondrites

Abstract— We performed a detailed study of silica‐rich components (SRC) in the paired CH chondrites Acfer 182 and 207. These SRCs appear either as chondrules or fragments, and they contribute <0.1 vol% to the bulk meteorite. They usually contain a silica and a silicate portion. Both portions are, in most cases, cryptocrystalline and have bulk SiO₂‐concentrations between 65 and 85 wt%. The silicate generally has a pyroxene normative composition. The silica often appears as blebs within the silicate matrix or vice versa. If there are no blebs, silica and silicate still form rounded interfaces. The SRCs are depleted in refractory elements like Ca, Al, and Ti relative to CI. A few SRC‐like objects are extremely rich in Mn and show no depletion in refractory elements. We conducted micro‐Raman studies on the silica portions of the SRCs to determine their structure, and we identified several silica phases: α‐quartz, cristobalite, glass, and a yet unidentified polymorph. The silicate portion is glass when the silica is glass and crystalline when the silica is crystalline. The low contents of Al and Ca make an igneous origin of the SRCs very unlikely, and the absence of metal excludes the formation by reduction of pyroxene. We suggest, instead, a fractional condensation origin of the SRCs from a Si‐enriched gas after removal of gaseous Mg by forsterite condensation. Additional evidence for fractional condensation is provided by a unique layered object with olivine in the core, pyroxene and metal at the rim, and silica at the outermost border; these layers record the condensation sequence. Two chondrules were found with several percent of Mn and high Cr, Na, and K contents, providing further evidence for condensation from a fractionated gas. The texture of the SRCs and the occurrence of cristobalite and silica glass, however, require formation by liquid immiscibility at high temperatures, above 1968 K, and subsequent fast cooling. Therefore, we propose a 2‐stage model for the formation of SRCs in CH chondrites: 1) fractional condensation of forsterite, enstatite, and SiO₂‐rich phases; and 2) reheating of SiO₂‐rich components to temperatures above 1968 K followed by rapid cooling. All other phases identified in CH chondrites can be understood within the framework of this model. Thus, the extremely unequilibrated CH chondrites provide a wealth of evidence for fractional condensation processes in the early solar nebula, in metals (Meibom et al. 1999), and in silicates.     

Condensation processes in astrophysical environments: The composition and structure of cometary grains

Abstract— We review the results of our recent experimental studies of astrophysical dust analogs. We discuss the condensation of amorphous silicates from mixed metal vapors, including evidence that such condensates form with metastable eutectic compositions. We consider the spectral evolution of amorphous magnesium silicate condensates as a function of time and temperature. Magnesium silicate smokes anneal readily at temperatures of about 1000–1100 K. In contrast we find that iron silicates require much higher temperatures (?1300 K) to bring about similar changes on the same timescale (days to months). We first apply these results to infrared space observatory observations of crystalline magnesium silicate grains around high‐mass‐outflow asymptotic giant branch stars in order to demonstrate their general utility in a rather simple environment. Finally, we apply these experimental results to infrared observations of comets and protostars in order to derive some interesting conclusions regarding large‐scale nebular dynamics, the natural production of organic molecules in protostellar nebulae, and the use of crystalline magnesium silicates as a relative indicator of a comet's formation age.     

Light noble gases and cosmogenic radionuclides in Estherville,Budulan, and other mesosiderites: Implications for exposure histories and production rates

Abstract— We report measurements of ²⁶AI, ¹⁰Be, ⁴¹Ca, and ³⁶Cl in the silicate and metal phases of 11 mesosiderites, including several specimens each of Budulan and Estherville, of the brecciated meteorite Bencubbin, and of the iron meteorite Udei Station. Average production rate ratios (atom/atom) for metal phase samples from Estherville and Budulan are ²⁶Al/¹⁰Be = 0.77 ± 0.02; ³⁶Cl/¹⁰Be = 5.3 ± 0.2. For a larger set of meteorites that includes iron meteorites and other mesosiderites, we find ²⁶Al/¹⁰Be = 0.72 ± 0.01 and ³⁶Cl/¹⁰Be = 4.5 ± 0.2. The average ⁴¹Ca/³⁶Cl production rate ratio is 1.10 ± 0.04 for metal separates from Estherville and four small iron falls. The ⁴¹Ca activities in dpm/(kg Ca) of various silicate separates from Budulan and Estherville span nearly a factor of 4, from <400 to >1600, indicating preatmospheric radii of >30 cm. After allowance for composition, the activities of ²⁶Al and ¹⁰Be (dpm/kg silicate) are similar to values measured in most ordinary chondrites and appear to depend only weakly on bulk Fe content. Unless shielding effects are larger than suggested by the ³⁶Cl and ⁴¹Ca activities of the metal phases, matrix effects are unimportant for ¹⁰Be and minor for ²⁶Al. Noble gas concentrations and isotopic abundances are reported for samples of Barea, Emery, Mincy, Morristown, and Marjalahti. New estimates of ³⁶Cl/³⁶Ar exposure ages for the metal phases agree well with published values. Neon‐21 production rates for mesosiderite silicates calculated from these ages and from measured ²¹Ne contents are consistently higher than predicted for L chondrites despite the fact that the mesosiderite silicates have lower Mg contents than L chondrites. We suggest that the elevation of the ²¹Ne production rate in mesosiderite silicates reflects a “matrix effect,” that is, the influence of the higher Fe content of mesosiderites, which acts to enhance the flux of low‐energy secondary particles and hence the ²¹Ne production from Mg. As ¹⁰Be production is relatively insensitive to this matrix effect, ¹⁰Be/²¹Ne ages give erroneously low production rates and high exposure ages. By coincidence, standard ²²Ne/²¹Ne based “shielding” corrections give fairly reliable ²¹Ne production rates in the mesosiderite silicates.