REE abundances in the matrix of the Allende (CV) meteorite: Implications for matrix origin

Abstract— The trace element distributions in the matrix of primitive chondrites were examined using four least‐contaminated matrix specimens from the polished sections of the Allende (CV) meteorite. Analysis of rare earth element (REE), Ba, Sr, Rb, and K abundances by isotope dilution mass spectrometry revealed that the elemental abundances of lithophile elements except for alkali metals (K, Rb) in the specimens of the Allende matrix studied here are nearly CI (carbonaceous Orgueil) chondritic (～1 × CI). Compared to refractory elements, all the matrix samples exhibited systematic depletion of the moderately volatile elements K and Rb (0.1–0.5 × CI). We suggest that the matrix precursor material did not carry significant amounts of alkali metals or that the alkalis were removed from the matrix precursor material during the parent body process and/or before matrix formation and accretion. The matrix specimens displayed slightly fractionated REE abundance patterns with positive Ce anomalies (CI‐normalized La/Yb ratio = 1.32–1.65; Ce/Ce* = 1.16–1.28; Eu/Eu* = 0.98–1.10). The REE features of the Allende matrix do not indicate a direct relationship with chondrules or calcium‐aluminum‐rich inclusions (CAIs), which in turn suggests that the matrix was not formed from materials produced by the breakage and disaggregation of the chondrules or CAIs. Therefore, we infer that the Allende matrix retains the REE features acquired during the condensation process in the nebula gas.     

DISTRIBUTION OF RARE EARTH ELEMENTS AND URANIUM IN VARIOUS COMPONENTS OF ORDINARY CHONDRITES

Rare earth elements (REE) and uranium were studied for their distributions in various component phases of four ordinary chondrites, Kesen (H4), Richardton (H5), Bruderheim (L6), and Saint Séverin (LL6). A selective dissolution method was applied for the phase fractionation. The REE were analysed by neutron activation analysis, and U was determined by neutron-induced fission tracks. The present study revealed that both REE and U are highly enriched in the Ca-phosphate minerals with different enrichment factors, implying chemical fractionation between them. The phosphates seem to be responsible for more than 80% of the light REE in all chondrites. On the other hand, only 20–40% of the total U resides in the Ca-phosphates. This difference in enrichments might have been caused through the levels of metamorphic activity on the meteoritic parent bodies.     

Detailed abundances of rare earth elements,thorium and uranium in chondritic meteorites: An ICP-MS study

Abstract— Inductively coupled plasma mass spectrometry (ICP-MS) was successfully applied to bulk samples of Allende, Jilin, Modoc, Saint-Séverin and Atlanta for the determination of rare earth elements (REE) (Y and 14 lanthanoids), Th and U. The results of ICP-MS showed good agreement with recommended values, and their reproducibilities were high enough to discuss the detailed abundances of lanthanoids and actinoids in chondritic meteorites. For the Allende reference sample issued by the Smithsonian Institution, a positive anomaly of Tm, a fractionation between light REE and heavy REE and a high Th/U ratio were observed in the CI-normalized abundances of REE, Th and U. These features are common for group II inclusions in Allende, suggesting that the abundances of refractory lithophiles in Allende are somewhat influenced by those in a specific constituent. For the other chondritic meteorites, a zigzag alteration was commonly observed in the heavy-REE region of their CI-normalized abundance patterns. It is suggested that such a zigzag pattern is attributable to erratically high abundances of monoisotopic REE (Tb, Ho and Tm) in the CI values. Abundances of REE, Th and U in the bulk samples are also discussed separately in detail.     

The formation conditions of enstatite chondrites: Insights from trace element geochemistry of olivine‐bearing chondrules in Sahara 97096 (EH3)

We report in situ LA‐ICP‐MS trace element analyses of silicate phases in olivine‐bearing chondrules in the Sahara 97096 (EH3) enstatite chondrite. Most olivine and enstatite present rare earth element (REE) patterns comparable to their counterparts in type I chondrules in ordinary chondrites. They thus likely share a similar igneous origin, likely under similar redox conditions. The mesostasis however frequently shows negative Eu and/or Yb (and more rarely Sm) anomalies, evidently out of equilibrium with olivine and enstatite. We suggest that this reflects crystallization of oldhamite during a sulfidation event, already inferred by others, during which the mesostasis was molten, where the complementary positive Eu and Yb anomalies exhibited by oldhamite would have possibly arisen due to a divalent state of these elements. Much of this igneous oldhamite would have been expelled from the chondrules, presumably by inertial acceleration or surface tension effects, and would have contributed to the high abundance of opaque nodules found outside them in EH chondrites. In two chondrules, olivine and enstatite exhibit negatively sloped REE patterns, which may be an extreme manifestation of a general phenomenon (possibly linked to near‐liquidus partitioning) underlying the overabundance of light REE observed in most chondrule silicates relative to equilibrium predictions. The silicate phases in one of these two chondrules show complementary Eu, Yb, and Sm anomalies providing direct evidence for the postulated occurrence of the divalent state for these elements at some stage in the formation reservoir of enstatite chondrites. Our work supports the idea that the peculiarities of enstatite chondrites may not require a condensation sequence at high C/O ratios as has long been believed.     

Northwest Africa 011: A “eucritic” basalt from a non‐eucrite parent body

Abstract— We have carried out a detailed petrographic, mineralogical, and trace element study of Northwest Africa (NWA) 011. This meteorite bears many similarities to the eucrites it was initially identified with, although oxygen isotopic compositions rule out a genetic relationship. Like many eucrites, NWA 011 crystallized from a source with approximately chondritic proportions of REE, although a slightly LREE‐enriched bulk composition with a small positive Eu anomaly, as well as highly fractionated Fe/Mg ratios and depleted Sc abundances (Korotchantseva et al. 2003), suggest that the NWA 011 source experienced some pyroxene and/or olivine fractionation. Thermal metamorphism resulted in homogenization of REE abundances within grains, but NWA 011 did not experience the intergrain REE redistribution seen in some highly metamorphosed eucrites. Despite a similarity in oxygen isotopic compositions, NWA 011 does not represent a basaltic partial melt from the acapulcoite/lodranite parent body. The material from which NWA 011 originated may have been like some CH or CB chondrites, members of the CR chondrite clan, which are all related through oxygen isotopic compositions. The NWA 011 parent body is probably of asteroidal origin, possibly the basaltic asteroid 1459 Magnya.     

Investigation of the dependence of rare-earth element abundances on the effective temperature and magnetic field in the atmospheres of chemically peculiar (Ap) stars

We have derived the abundances of the rare-earth elements (REEs) Ce, Pr, Nd, and Eu in the atmospheres of 26 magnetic peculiar (Ap) stars in the range of effective temperatures 7000–10 000 K from spectra with resolutions R = 48 000 and 80 000 and investigated the dependence of the CePrNdEu anomalies (the difference in the element abundances determined separately from lines of the first and second ionization stages) on the effective temperature. The REE anomaly is shown to decrease with increasing effective temperature virtually to the point of disappearance for all of the investigated elements, except Eu. For the best-studied element Nd the Nd anomaly has also been found to decrease with increasing magnetic field strength for cool stars. For hot stars there is no Nd anomaly in a wide range of magnetic field strengths. Since the presence of anomalies in cool Ap stars is associated with the REE concentration in the upper atmospheric layers, the lower boundary of the REE layer apparently sinks into deeper layers with increasing effective temperature and magnetic field, causing the anomalies to disappear. We have detected an anticorrelation between the abundances of iron-peak elements and rare-earth elements, which serves as additional evidence for different stratification of these elements in the atmospheres of Ap stars.     

Mineralogy and chemistry of Rumuruti: The first meteorite fall of the new R chondrite group

Abstract— The Rumuruti meteorite shower fell in Rumuruti, Kenya, on 1934 January 28 at 10:43 p.m. Rumuruti is an olivine-rich chondritic breccia with light-dark structure. Based on the coexistence of highly recrystallized fragments and unequilibrated components, Rumuruti is classified as a type 3–6 chondrite breccia. The most abundant phase of Rumuruti is olivine (mostly Fa_～39) with about 70 vol%. Feldspar (～14 vol%; mainly plagioclase), Ca-pyroxene (5 vol%), pyrrhotite (4.4 vol%), and pentlandite (3.6 vol%) are major constituents. All other phases have abundances below 1 vol%, including low-Ca pyroxene, chrome spinels, phosphates (chlorapatite and whitlockite), chalcopyrite, ilmenite, tridymite, Ni-rich and Ge-containing metals, kamacite, and various particles enriched in noble metals like Pt, Ir, arid Au. The chemical composition of Rumuruti is chondritic. The depletion in refractory elements (Sc, REE, etc.) and the comparatively high Mn, Na, and K contents are characteristic of ordinary chondrites and distinguish Rumuruti from carbonaceous chondrites. However, S, Se, and Zn contents in Rumuruti are significantly above the level expected for ordinary chondrites. The oxygen isotope composition of Rumuruti is high in δ¹⁷O (5.52 ‰) and δ¹⁸O (5.07 ‰). Previously, a small number of chondritic meteorites with strong similarities to Rumuruti were described. They were called Carlisle Lakes-type chondrites and they comprise: Carlisle Lakes, ALH85151, Y-75302, Y-793575, Y-82002, Acfer 217, PCA91002, and PCA91241, as well as clasts in the Weatherford chondrite. All these meteorites are finds from hot and cold deserts having experienced various degrees of weathering. With Rumuruti, the first meteorite fall has been recognized that preserves the primary mineralogical and chemical characteristics of a new group of meteorites. Comparing all chondrites, the characteristic features can be summarized as follows: (a) basically chondritic chemistry with ordinary chondrite element patterns of refractory and moderately volatile lithophiles but higher abundances of S, Se, and Zn; (b) high degree of oxidation (37–41 mol% Fa in olivine, only traces of Fe, Ni-metals, occurrence of chalcopyrite); (c) exceptionally high Δ¹⁷O values of about 2.7 for bulk samples; (d) high modal abundance of olivine (～70 vol%); (e) Ti-Fe³⁺?rich chromite (～5.5 wt% TiO₂); (f) occurrence of various noble metal-rich particles; (g) abundant chondritic breccias consisting of equilibrated clasts and unequilibrated lithologies. With Rumuruti, nine meteorite samples exist that are chemically and mineralogically very similar. These meteorites are attributed to at least eight different fall events. It is proposed in this paper to call this group R chondrites (rumurutiites) after the first and only fall among these meteorites. These meteorites have a close relationship to ordinary chondrites. However, they are more oxidized than any of the existing groups of ordinary chondrites. Small, but significant differences in chemical composition and in oxygen isotopes between R chondrites and ordinary chondrites exclude formation of R chondrites from ordinary chondrites by oxidation. This implies a separate, independent R chondrite parent body.     

Chemical and physical studies of type 3 chondrites XII: The metamorphic history of CV chondrites and their components

Abstract— The induced thermoluminescence (TL) properties of 16 CV and CV-related chondrites, four CK chondrites and Renazzo (CR2) have been measured in order to investigate their metamorphic history. The petrographic, mineralogical and bulk compositional differences among the CV chondrites indicate that the TL sensitivity of the ～130 °C TL peak is reflecting the abundance of ordered feldspar, especially in chondrule mesostasis, which in turn reflects parent-body metamorphism. The TL properties of 18 samples of homogenized Allende powder heated at a variety of times and temperatures, and cathodoluminescence mosaics of Axtell and Coolidge, showed results consistent with this conclusion. Five refractory inclusions from Allende, and separates from those inclusions, were also examined and yielded trends reflecting variations in mineralogy indicative of high peak temperatures (either metamorphic or igneous) and fairly rapid cooling. The CK chondrites are unique among metamorphosed chondrites in showing no detectable induced TL, which is consistent with literature data that suggests very unusual feldspar in these meteorites. Using TL sensitivity and several mineral systems and allowing for the differences in the oxidized and reduced subgroups, the CV and CV-related meteorites can be divided into petrologic types analogous to those of the ordinary and CO type 3 chondrites. Axtell, Kaba, Leoville, Bali, Arch and ALHA81003 are type 3.0–3.1, while ALH84018, Efremovka, Grosnaja, Allende and Vigarano are type 3.2–3.3 and Coolidge and Loongana 001 are type 3.8. Mokoia is probably a breccia with regions ranging in petrologic type from 3.0 to 3.2. Renazzo often plots at the end of the reduced and oxidized CV chondrite trends, even when those trends diverge, suggesting that in many respects it resembles the unmetamorphosed precursors of the CV chondrites. The low-petrographic types and low-TL peak temperatures of all samples, including the CV3.8 chondrites, indicates metamorphism in the stability field of low feldspar (i.e., <800 °C) and a metamorphic history similar to that of the CO chondrites but unlike that of the ordinary chondrites.     

Chemical and oxygen isotopic properties of ordinary chondrites (H5, L6) from Oman: Signs of isotopic equilibrium during thermal metamorphism

Mean bulk chemical data of recently found H5 and L6 ordinary chondrites from the deserts of Oman generally reflect isochemical features which are consistent with the progressive thermal metamorphism of a common, unequilibrated starting material. Relative differences in abundances range from 0.5–10% in REE (Eu = 14%), 6–13% in siderophile elements (Co = 48%), and >10% in lithophile elements (exceptions are Ba, Sr, Zr, Hf, U = >30%) between H5 and L6 groups. These differences may have accounted for variable temperature conditions during metamorphism on their parent bodies. The CI/Mg‐normalized mean abundances of refractory lithophile elements (Al, Ca, Sm, Yb, Lu, V) show no resolvable differences between H5 and L6 suggesting that both groups have experienced the same fractionation. The REE diagram shows subtle enrichment in LREE with a flat HREE pattern. Furthermore, overall mean REE abundances are ~0.6 × CI with enriched La abundance (~0.9 × CI) in both groups. Precise oxygen isotope compositions demonstrate the attainment of isotopic equilibrium by progressive thermal metamorphism following a mass‐dependent isotope fractionation trend. Both groups show a ~slope‐1/2 line on a three‐isotope plot with subtle negative deviation in ?¹⁷O associated with δ¹⁸O enrichment relative to δ¹⁷O. These deviations are interpreted as the result of liberation of water from phyllosilicates and evaporation of a fraction of the water during thermal metamorphism. The resultant isotope fractionations caused by the water loss are analogous to those occurring between silicate melt and gas phase during CAI and chondrule formation in chondrites and are controlled by cooling rates and exchange efficiency.     

Phosphate and feldspar mineralogy of equilibrated L chondrites: The record of metasomatism during metamorphism in ordinary chondrite parent bodies

In ordinary chondrites (OCs), phosphates and feldspar are secondary minerals known to be the products of parent‐body metamorphism. Both minerals provide evidence that metasomatic fluids played a role during metamorphism. We studied the petrology and chemistry of phosphates and feldspar in petrologic type 4–6 L chondrites, to examine the role of metasomatic fluids, and to compare metamorphic conditions across all three OC groups. Apatite in L chondrites is Cl‐rich, similar to H chondrites, whereas apatite in LL chondrites has lower Cl/F ratios. Merrillite has similar compositions among the three chondrite groups. Feldspar in L chondrites shows a similar equilibration trend to LL chondrites, from a wide range of plagioclase compositions in petrologic type 4 to a homogeneous albitic composition in type 6. This contrasts with H chondrites which have homogeneous albitic plagioclase in petrologic types 4–6. Alkali‐ and halogen‐rich and likely hydrous metasomatic fluids acted during prograde metamorphism on OC parent bodies, resulting in albitization reactions and development of phosphate minerals. Fluid compositions transitioned to a more anhydrous, Cl‐rich composition after the asteroid began to cool. Differences in secondary minerals between H and L, LL chondrites can be explained by differences in fluid abundance, duration, or timing of fluid release. Phosphate minerals in the regolith breccia, Kendleton, show lithology‐dependent apatite compositions. Bulk Cl/F ratios for OCs inferred from apatite compositions are higher than measured bulk chondrite values, suggesting that bulk F abundances are overestimated and that bulk Cl/F ratios in OCs are similar to CI.     

Origin of fayalitic olivine rims and lath-shaped matrix olivine in the CV3 chondrite Allende and its dark inclusions

Abstract— We have studied an Allende dark inclusion by optical microscopy, scanning electron microscopy, electron microprobe analysis and transmission electron microscopy. The inclusion consists of chondrules, isolated olivines and matrix, which, as in the Allende host, is mainly composed of 5–20 μm long lath-shaped fayalitic grains with a narrow compositional range (Fa_{42 ± 2}) and nepheline. Olivine phenocrysts in chondrules and isolated olivine grains show various degrees of replacement by 5–10 μm wide fayalitic rims (Fa_{39 ± 2}) and 100–1000 μm wide translucent zones, which consist of 5–20 μm long lath-shaped fayalitic grains (Fa_{41 ± 1}) intergrown with nepheline. These fayalitic olivines, like those in the matrix of the dark inclusion, contain 10–20 nm sized inclusions of chromite, hercynite, and Fe-Ni sulfides. The fayalitic rims around remnant olivines are texturally and compositionally identical to those in Allende host, suggesting that they have similar origins. Chondrules are surrounded by opaque rims consisting of tiny lath-shaped fayalitic olivines (<1–3 μm long) intergrown with nepheline. As in the Allende host, fayalitic olivine veins may crosscut altered chondrules, fine-grained chondrule rims and extend into the matrix, indicating that alteration occurred after accretion. We infer that fayalitic olivine rims and lath-shaped fayalites in Allende and its dark inclusions formed from phyllosilicate intermediate phases. This explanation accounts for (1) the similarity of the replacement textures observed in the dark inclusion and Allende host to aqueous alteration textures in CM chondrites; (2) the anomalously high abundances of Al and Cr and the presence of tiny inclusions of spinels and sulfides in fayalitic olivines in Allende and Allende dark inclusions; (3) abundant voids and defects in lath-shaped fayalites in the Allende dark inclusion, which may be analogous to those in partly dehydrated phyllosilicates in metamorphosed CM/CI chondrites. We conclude that the matrix and chondrule rims in Allende were largely converted to phyllosilicates and then completely dehydrated. The Allende dark inclusions experienced diverse degrees of aqueous/hydrothermal alteration prior to complete dehydration. The absence of low-Ca pyroxene in the dark inclusion and its significant replacement by fayalitic olivine in Allende is consistent with the lower resistance of low-Ca pyroxene to aqueous alteration relative to forsteritic olivine. Hydro-thermal processing of Allende probably also accounts for the low abundance of planetary noble gases and interstellar grains, and the formation of nepheline, sodalite, salite-hedenbergite pyroxenes, wollastonite, kirschsteinite and andradite in chondrules and Ca,Al-rich inclusions.     

Modification of REE distribution of ordinary chondrites from Atacama (Chile) and Lut (Iran) hot deserts: Insights into the chemical weathering of meteorites

The behavior of rare earth elements (REEs) during hot desert weathering of meteorites is investigated. Ordinary chondrites (OCs) from Atacama (Chile) and Lut (Iran) deserts show different variations in REE composition during this process. Inductively coupled plasma–mass spectrometry (ICP‐MS) data reveal that hot desert OCs tend to show elevated light REE concentrations, relative to OC falls. Chondrites from Atacama are by far the most enriched in REEs and this enrichment is not necessarily related to their degree of weathering. Positive Ce anomaly of fresh chondrites from Atacama and the successive formation of a negative Ce anomaly with the addition of trivalent REEs are similar to the process reported from Antarctic eucrites. In addition to REEs, Sr and Ba also show different concentrations when comparing OCs from different hot deserts. The stability of Atacama surfaces and the associated old terrestrial ages of meteorites from this region give the samples the necessary time to interact with the terrestrial environment and to be chemically modified. Higher REE contents and LREE‐enriched composition are evidence of contamination by terrestrial soil. Despite their low degrees of weathering, special care must be taken into account while working on the REE composition of Atacama meteorites for cosmochemistry applications. In contrast, chondrites from the Lut desert show lower degrees of REE modification, despite significant weathering signed by Sr content. This is explained by the relatively rapid weathering rate of the meteorites occurring in the Lut desert, which hampers the penetration of terrestrial material by forming voluminous Fe oxide/oxyhydroxides shortly after the meteorite fall.     

Origin of the metamorphosed clasts in the CV3 carbonaceous chondrite breccias of Graves Nunataks 06101, Vigarano,Roberts Massif 04143, and Yamato‐86009

We observed metamorphosed clasts in the CV3 chondrite breccias Graves Nunataks 06101, Vigarano, Roberts Massif 04143, and Yamato‐86009. These clasts are coarse‐grained polymineralic rocks composed of Ca‐bearing ferroan olivine (Fa_24–40, up to 0.6 wt% CaO), diopside (Fs_7–12Wo_44–50), plagioclase (An_52–75), Cr‐spinel (Cr/[Cr + Al] = 0.4, Fe/[Fe + Mg] = 0.7), sulfide and rare grains of Fe‐Ni metal, phosphate, and Ca‐poor pyroxene (Fs₂₄Wo₄). Most clasts have triple junctions between silicate grains. The rare earth element (REE) abundances are high in diopside (REE ~3.80–13.83 × CI) and plagioclase (Eu ~12.31–14.67 × CI) but are low in olivine (REE ~0.01–1.44 × CI) and spinel (REE ~0.25–0.49 × CI). These REE abundances are different from those of metamorphosed chondrites, primitive achondrites, and achondrites, suggesting that the clasts are not fragments of these meteorites. Similar mineralogical characteristics of the clasts with those in the Mokoia and Yamato‐86009 breccias (Jogo et al. 2012 ) suggest that the clasts observed in this study would also form inside the CV3 chondrite parent body. Thermal modeling suggests that in order to reach the metamorphosed temperatures of the clasts of >800 °C, the clast parent body should have accreted by ~2.5–2.6 Ma after CAIs formation. The consistency of the accretion age of the clast parent body and the CV3 chondrule formation age suggests that the clasts and CV3 chondrites could be originated from the same parent body with a peak temperature of 800–1100 °C. If the body has a peak temperature of >1100 °C, the accretion age of the body becomes older than the CV3 chondrule formation age and multiple CV3 parent bodies are likely.     

Minor element zoning and trace element geochemistry of pallasites

Abstract— I report here on an ion probe study of minor element spatial distributions and trace element concentrations in six pallasites. Pallasite olivines exhibit ubiquitous minor element zoning that is independent of grain size, morphology, and adjacent phases. Ca, Cr, Ti, V, and Ni concentrations decrease from center to rim by factors of up to 10, while Mn is generally unzoned or increases slightly at the very edge of some olivine grains. The maximum concentrations of these elements at the center of olivine vary from grain to grain within the same meteorite and among the pallasites studied. These zoning profiles are consistent with thermal diffusion during rapid cooling. The inferred cooling rates at high temperature regimes are orders of magnitude faster than the low‐temperature metallographic cooling rates (?0.5 to 2°C/Ma). This suggests that pallasites, like mesosiderites, have experienced rather complicated thermal histories, i.e., cooling rapidly at high temperatures and slowly at low temperatures. Pallasite olivines are essentially free of REEs. However, the phosphates display a wide range of REE abundances (0.001 to 100 x CI) with distinct patterns. REEs are generally homogeneous within a given grain but vary significantly from grain to grain by a factor of up to 100. Albin and Imilac whitlockite are highly enriched in HREEs (?50 x CI) but are relatively depleted in LREEs (?0.1 to 1 x CI). Eagle Station whitlockite has a very unusual REE pattern: flat LREEs at a 0.1 x CI level, a large positive Eu anomaly, and a sharp increase from Gd (0.1 x CI) to Lu (70 x CI). Eagle Station stanfieldite has a similar REE pattern to that of whitlockite but with much lower REEs by a factor of 10 to 100. Springwater farringtonite has relatively low REE concentrations (0.001 to 1 x CI) with a highly fractionated HREE‐enriched pattern (CI‐normalized Lu/La ?100). Postulating any igneous processes that could have fractionated REEs in these phosphates is difficult. Possibly, phosphates were incorporated into pallasites during mixing of olivine and IIIAB‐like molten Fe. These phosphates preserve characteristics of a previous history. Pallasites have not necessarily formed at the mantle‐core boundary of their parent bodies. The pallasite thermal histories suggest that pallasites may have formed at a shallow depth and were subsequently buried deep under a regolith blanket.     

GENESIS OF THE CUMULATE EUCRITES SERRA DE MAGÉ AND MOORE COUNTY: A GEOCHEMICAL STUDY

Major, minor and trace element abundances have been determined by instrumental neutron activation analysis (INAA) in whole rock and plagioclase separates of Serra de Magé (SdM). The whole rock contains 52% normative plagioclase and its chondritic normalized REE abundance pattern shows a large Eu anomaly, dominated by the plagioclase REE distribution, and nearly unfractionated La-Sm and Sm-Lu abundances. The plagioclase separates contained ～ 6% pyroxenes and exhibited a typical plagioclase REE distribution. The REE abundances in the derivative equilibrium magmas from which SdM and Moore County (MC) plagioclases crystallized have been estimated from the plagioclase data and the plagioclase mineral/liquid partition coefficients. The REE distributions in possibly earlier parental magmas were calculated by assuming that various degrees of plagioclase and pigeonite (plagioclase/pigeonite = 1) fractional crystallization had been operative prior to the crystallization of SdM and MC. The calculated La/Sm and Sm/Yb ratios for the earlier magmas are essentially the same as the equilibrium magmas over a wide range (10–95%) of the assumed fractional crystallization. Considering the REE distributions and the Fe/Fe+Mg ratios, calculation shows that there is no simple genetic relationship between MC and SdM via fractional crystallization processes. A hypothesis for the derivation of these cumulate eucrites in the plutonic environment from residual diogenitic liquid, which was produced by the extensive partial melting of an eucritic source material followed by the crystallization of diogenite, also fails to account for the fractionated REE patterns calculated for the equilibrium and the possible parental magmas for either SdM or MC. Equilibrium non-modal partial melting calculations indicate that SdM and MC could be genetically related by a factor ～ 6 difference in the degrees of partial melting from a similar source material. However, this common source material which should contain > 30% high-Ca clinopyroxene and has a chondritic normalized La/Yb ～ 3, is different than that proposed for the non-cumulate eucrites.     

Impact-induced chondrule flattening in the Allende CV3 carbonaceous chondrite: Shock experiments

Abstract— We have carried out shock-recovery experiments on the Allende CV3 carbonaceous chondrite using a single-stage propellant gun and succeeded in reproducing oriented, flattened chondrules like those observed in some natural CV3 chondrites. The Allende samples were shocked at equilibrium pressures of 11 and 21 GPa, which are close to the highest values in shock stages S2 and S3, respectively (Stöffler et al., 1991). Chondrules are flattened nearly perpendicular to the compaction axis with mean aspect ratios of 1.34 and 1.62 at pressures of 11 and 21 GPa, respectively; thus, the degree of chondrule flattening is proportional to the shock intensity. The chondrule flattening and foliation are mainly due to collapse of pores in the matrix under shock pressure. High matrix abundance of CV3 chondrites could result in much apparent chondrule flattening relative to ordinary chondrites. Optical and electron microscope observations show that textural and mineralogical characteristics of chondrules and matrix in the shock-loaded samples are very similar to those observed in naturally shocked CV3 chondrites. Our results provide strong support for the interpretation that the chondrule flattening and foliation in CV3 chondrites were caused by shock-induced pressure due to hypervelocity impacts on the meteorite parent bodies.     

Petrographic comparison of refractory inclusions from different chemical groups of chondrites

Abstract— Twenty‐four refractory inclusions (40–230 μm, with average of 86 ± 40 μm) were found by X‐ray mapping of 18 ordinary chondrites. All inclusions are heavily altered, consisting of finegrained feldspathoids, spinel, and Ca‐pyroxene with minor ilmenite. The presence of feldspathoids and lack of melilite are due to alteration that took place under oxidizing conditions as indicated by FeO‐ZnO‐rich spinel and ilmenite. The pre‐altered mineral assemblages are dominated by two types: one rich in melilite, referred to as type A‐like, and the other rich in spinel, referred to as spinelpyroxene inclusions. This study and previous data show similar type and size distributions of refractory inclusions in ordinary and enstatite chondrites. A survey of refractory inclusions was also conducted on Allende and Murchison in order to make unbiased comparison with their counterparts in other chondrites. The predominant inclusions are type A and spinel‐pyroxene, with average sizes of 170 ± 130 μm (except for two mm‐sized inclusions) in Allende and 150 ± 100 μm in Murchison. The relatively larger sizes are partially due to common conglomerating of smaller nodules in both chondrites. The survey reveals closely similar type and size distributions of refractory inclusions in various chondrites, consistent with our previous data of other carbonaceous chondrites. The petrographic observations suggest that refractory inclusions in various groups of chondrites had primarily formed under similar processes and conditions, and were transported to different chondrite‐accreting regions. Heterogeneous abundance and distinct alteration assemblages of refractory inclusions from various chondrites could be contributed to transporting processes and secondary reactions under different conditions.     

Analysis of ordinary chondrites using powder X‐ray diffraction: 2. Applications to ordinary chondrite parent‐body processes

Abstract– We evaluate the chemical and physical conditions of metamorphism in ordinary chondrite parent bodies using X‐ray diffraction (XRD)‐measured modal mineral abundances and geochemical analyses of 48 type 4–6 ordinary chondrites. Several observations indicate that oxidation may have occurred during progressive metamorphism of equilibrated chondrites, including systematic changes with petrologic type in XRD‐derived olivine and low‐Ca pyroxene abundances, increasing ratios of MgO/(MgO+FeO) in olivine and pyroxene, mean Ni/Fe and Co/Fe ratios in bulk metal with increasing metamorphic grade, and linear Fe addition trends in molar Fe/Mn and Fe/Mg plots. An aqueous fluid, likely incorporated as hydrous silicates and distributed homogeneously throughout the parent body, was responsible for oxidation. Based on mass balance calculations, a minimum of 0.3–0.4 wt% H₂O reacted with metal to produce oxidized Fe. Prior to oxidation the parent body underwent a period of reduction, as evidenced by the unequilibrated chondrites. Unlike olivine and pyroxene, average plagioclase abundances do not show any systematic changes with increasing petrologic type. Based on this observation and a comparison of modal and normative plagioclase abundances, we suggest that plagioclase completely crystallized from glass by type 4 temperature conditions in the H and L chondrites and by type 5 in the LL chondrites. Because the validity of using the plagioclase thermometer to determine peak temperatures rests on the assumption that plagioclase continued to crystallize through type 6 conditions, we suggest that temperatures calculated using pyroxene goethermometry provide more accurate estimates of the peak temperatures reached in ordinary chondrite parent bodies.     

A database of chondrite analyses including platinum group elements,Ni, Co,Au, and Cr: Implications for the identification of chondritic projectiles

Abstract— Siderophile elements have been used to constrain projectile compositions in terrestrial and lunar impact melt rocks. To obtain a better knowledge of compositional differences between potential chondritic projectile types, meteorite analyses of the elements Ru, Rh, Pd, Os, Ir, Pt, Cr, Co, Ni, and Au were gathered into a database. The presented compilation comprises 806 analyses of 278 chondrites including new ICP‐MS analyses of Allende and two ordinary chondrites. Each data set was evaluated by comparing element ratios of meteorites from the same chondrite group. Characteristic element abundances and ratios were determined for each group. Features observed in the element abundance patterns can be linked directly to the presence of certain components, such as the abundance of refractory elements Os, Ir, and Ru correlating with the occurrence of refractory inclusions in CV, CO, CK, and CM chondrites. The refined characteristic element ratios appear to be representative not only for meteorites, but also for related asteroidal bodies. Chondrite element ratios were compared to previously published values from impact melt rocks of the Popigai and Morokweng impact structures confirming that an identification of the specific type of projectile (L and LL chondrite, respectively) is possible. The assessment for Morokweng is supported by the recent discovery of an LL chondrite fragment in the impact melt rocks. Ultimately, the database provides valuable information for understanding processes in the solar nebula as they are recorded in chondrites. A new type of complementarity between element patterns of CK and EH chondrites is suggested to be the result of condensation, redox, and transportation processes in the solar nebula.     

Re‐examining the role of chondrules in producing the elemental fractionations in chondrites

Abstract— The matrices of all primitive chondrites contain presolar materials (circumstellar grains and interstellar organics) in roughly CI abundances, suggesting that all chondrites accreted matrix that is dominated by a CI‐like component. The matrix‐normalized abundances of the more volatile elements (condensation temperatures <750–800 K) in carbonaceous and ordinary chondrites are also at or slightly above CI levels. The modest excesses may be due to low levels of these elements in chondrules and associated metal. Subtraction of a CI‐like matrix component from a bulk ordinary chondrite composition closely matches the average composition of chondrules determined by instrumental neutron activation analysis (INAA) if some Fe‐metal is added to the chondrule composition. Measured matrix compositions are not CI‐like. Sampling bias and secondary redistribution of elements may have played a role, but the best explanation is that ?10–30% of refractory‐rich, volatile depleted material was added to matrix. If most of the more volatile elements are in a CI‐dominated matrix, the major and volatile element fractionations must be largely carried by chondrules. There is both direct and indirect evidence for evaporation during chondrule formation. Type IIA and type B chondrules could have formed from a mixture of CI material and material evaporated from type IA chondrules. The Mg‐Si‐Fe fractionations in the ordinary chondrites can be reproduced with the loss of type IA chondrule material and associated metal. The loss of evaporated material from the chondrules could explain the volatile element fractionations. Mechanisms for how these fractionations occurred are necessarily speculative, but two possibilities are briefly explored.