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Oxygen isotope and trace element data for 13 samples of the Kaidun chondritic breccia reaffirm the complex polymict nature of this unique meteorite. Bulk Kaidun samples most closely resemble CR chondrites, but the matrix is CI-like. Two separated clasts are CR-like but have some properties that resemble CM, two clasts are enstatite chondrites (one EL and one EH), one clast is an aubrite-like metal-rich impact melt, and one clast is a unique layered olivine-bearing pyroxenite with the isotopic composition of an aubrite. Yet, although each clast resembles a known meteorite group, all deviate in some respect from the norms for those groups. Collectively, Kaidun has sampled materials not yet represented in the world meteorite collections and which greatly extend the definitions of known meteorite groups. Phyllosilicates in Kaidun span a very wide range in composition and vary from clast to clast, suggesting that the aqueous alteration experienced by the clasts predated assembly of the Kaidun parent body.

Laboratory studies of vacuum dehydration of Mg-O-H units in minerals and rocks reveal large kinetic isotope effects in oxygen, with light-isotope enrichment in the liberated water, and concomitant heavy-isotope enrichment in the residual solids. Application of the same techniques to a meteorite assemblage including hydrous magnesium silicates shows a much more complex behavior, probably due to isotopic heterogeneity inherited from processes on the meteorite parent body. Measurements of both the 17 O/ 16 O variations and the 18 O/ 16 O variations confirm theoretical predictions that slopes of three-isotope correlation lines are systematically larger for equilibrium isotope effects than for kinetic isotope effects.

Bulk chemical and O-, Mg- and Si-isotopic compositions were measured for each of 17 Types A and B refractory inclusions from CV3 chondrites. After bulk chemical compositions were corrected for non-representative sampling in the laboratory, the Mg- and Si-isotopic compositions of each inclusion were used to calculate its original chemical composition assuming that the heavy-isotope enrichments of these elements are due to Rayleigh fractionation that accompanied their evaporation from CMAS liquids. The resulting pre-evaporation chemical compositions are consistent with those predicted by equilibrium thermodynamic calculations for high-temperature nebular condensates, but only if different inclusions condensed from nebular regions that ranged in total pressure from 10−6 to 10−1 bar, regardless of whether they formed in a system of solar composition or in one enriched in dust of ordinary chondrite composition relative to gas by a factor of 10 compared to solar composition. This is similar to the range of total pressures predicted by dynamic models of the solar nebula for regions whose temperatures are in the range of silicate condensation temperatures. Alternatively, if departure from equilibrium condensation and/or non-representative sampling of condensates in the nebula occurred, the inferred range of total pressure could be smaller. Simple kinetic modeling of evaporation successfully reproduces observed chemical compositions of most inclusions from their inferred pre-evaporation compositions, suggesting that closed-system isotopic exchange processes did not have a significant effect on their isotopic compositions. Comparison of pre-evaporation compositions with observed ones indicates that 80% of the enrichment in refractory CaO + Al2O3 relative to more volatile MgO + SiO2 is due to initial condensation and 20% due to subsequent evaporation for both Types A and B inclusions.

On the night of March 26, 2003, a large meteorite broke up and fell upon the south suburbs of Chicago. The name Park Forest, for the village that is at the center of the strewnfield, has been approved by the nomenclature committee of the Meteoritical Society. Satellite data indicate that the bolide traveled from the southwest toward the northeast. The strewnfield has a southeast-northwest trend; however, this is probably due to the effects of strong westerly winds at high altitudes. Its very low 56Co and very high 60Co activities indicate that Park Forest had a preatmospheric mass that was at least ~900 kg and could have been as large as ~7 x 10^3 kg, of which only ~30 kg have been recovered. The average compositions of olivine and low-Ca pyroxene, Fa24.7 ± 1.1 and Fs20.8 ± 0.7, respectively, and its bulk oxygen isotopic composition, δ18O = +4.68‰, δ17O = +3.44‰, show that Park Forest is an L chondrite. The ferromagnesian minerals are well equilibrated, chondrules are easily recognized, and maskelynite is mostly ≤50 μm across. Based on these observations, we classify Park Forest as type 5. The meteorite has been strongly shocked, and based on the presence of maskelynite, mosaicism and planar deformation features in olivine, undulatory extinction in pyroxene, and glassy veins, the shock stage is S5. The meteorite is a monomict breccia, consisting of light-colored, angular to rounded clasts in a very dark host. The light and dark lithologies have essentially identical mineral and oxygen isotopic compositions. Their striking difference in appearance is due to the presence of a fine, pervasive network of sulfide veins in the dark lithology, resulting in very short optical path lengths. The dark lithology probably formed from the light lithology in an impact that formed a sulfide-rich melt and injected it into cracks.

Gujba is a coarse-grained meteorite fall composed of 41 vol% large kamacite globules, 20 vol% large light-colored silicate globules with cryptocrystalline, barred pyroxene and barred olivine textures, 39 vol% dark-colored, silicate-rich matrix, and rare refractory inclusions. Gujba resembles Bencubbin and Weatherford in texture, oxygen-isotopic composition and in having high bulk delta N-15 values (approximately +685%0). The He-3 cosmic-ray exposure age of Gujba (26 +/- 7 Ma) is essentially identical to that of Bencubbin, suggesting that they were both reduced to meter-size fragments in the same parent-body collision. The Gujba metal globules exhibit metal-troilite quench textures and vary in their abundances of troilite and volatile siderophile elements. We suggest that the metal globules formed as liquid droplets either via condensation in an impact-generated vapor plume or by evaporation of preexisting metal particles in a plume. The lower the abundance of volatile elements in the metal globules, the higher the globule quench temperature. We infer that the large silicate globules also formed from completely molten droplets; their low volatile-element abundances indicate that they also formed at high temperatures, probably by processes analogous to those that formed the metal globules. The coarse-grained Bencubbin-Weatherford-Gujba meteorites may represent a depositional component from the vapor cloud enriched in coarse and dense particles. A second class of Bencubbin-like meteorites (represented by Hammadah a1 Hamra 237 and QUE 94411) may be a finer fraction derived from the same vapor cloud

The meteorite Northwest Africa 773 (NWA 773) is a lunar sample with implications for the evolution of mafic magmas on the moon. A combination of key parameters including whole-rock oxygen isotopic composition, Fe/Mn ratios in mafic silicates, noble gas concentrations, a KREEP-like rare earth element pattern, and the presence of regolith agglutinate fragments indicate a lunar origin for NWA 773. Partial maskelynitization of feldspar and occasional twinning of pyroxene are attributed to shock deformation. Terrestrial weathering has caused fracturing and precipitation of Carich carbonates and sulfates in the fractures, but lunar minerals appear fresh and unoxidized. The meteorite is composed of two distinct lithologies: a two-pyroxene olivine gabbro with cumulate texture, and a polymict, fragmental regolith breccia. The olivine gabbro is dominated by cumulate olivine with pigeonite, augite, and interstitial plagioclase feldspar. The breccia consists of several types of clasts but is dominated by clasts from the gabbro and more FeO-rich derivatives. Variations in clast mineral assemblage and pyroxene Mg/(Mg + Fe) and Ti/(Ti + Cr) record an igneous Fe-enrichment trend that culminated in crystallization of fayalite + silica + hedenbergitebearing symplectites. The Fe-enrichment trend and cumulate textures observed in NWA 773 are similar to features of terrestrial ponded lava flows and shallow-level mafic intrusives, indicating that NWA 773 may be from a layered mafic intrusion or a thick, differentiated lava flow. NWA 773 and several other mafic lunar meteorites have LREE-enriched patters distinct from Apollo and Luna mare basalts, which tend to be LREE-depleted. This is somewhat surprising in light of remote sensing data that indicates that the Apollo and Luna missions sampled a portion of the moon that was enriched in incompatible heatproducing elements.

In this paper we report petrological and chemical data of the unusual chondritic meteorites Yamato (Y)-792947, Y-93408 and Y-82038. The three meteorites are very similar in texture and chemical composition, suggesting that they are pieces of a single fall. The whole-rock oxygen isotopes and the chemical compositions are indicative ofH chondrites. In addition, the mineralogy, and the abundances of chondrule types, opaque minerals and matrices suggest that these meteorites are H3 chondrites. They were hardly affected by thermal and shock metamorphism. The degree of weathering is very low. We conclude that these are the most primitive H chondrites, H3.2-3.4 (SI), known to date. On the other hand, these chondrites contain extraordinarily high amounts of refractory inclusions, intermediate between those of ordinary and carbonaceous chondrites. The distribution of the inclusions may have been highly heterogeneous in the primitive solar nebula. The mineralogy, chemistry and oxygen isotopic compositions of inclusions studied here are similar to those in CO and E chondrites.

Dhofar 019 is a new martian meteorite found in the desert of Oman. In texture, mineralogy, and major and trace element chemistry, this meteorite is classified as a basaltic shergottite. Olivine megacrysts are set within a groundmass composed of finer grained olivine, pyroxene (pigeonite and augite), and maskelynite. Minor phases are chromite-ulvospinel, ilmenite, silica, K-rich feldspar, merrillite, chlorapatite, and pyrrhotite. Secondary phases of terrestrial origin include calcite, gypsum, celestite, Fe hydroxides, and smectite. Dhofar 019 is most similar to the Elephant Moraine (EETA) 79001 lithology A and Dar al Gani (DaG) 476/489 shergottites. The main features that distinguish Dhofar 019 from other shergottites are lack of orthopyroxene; lower Ni contents of olivine; the heaviest oxygen-isotopic bulk composition; and larger compositional ranges for olivine, maskelynite, and spinel, as well as a wide range for pyroxenes. The large compositional ranges of the minerals are indicative of relatively rapid crystallization. Modeling of olivine chemical zonations yield minimum cooling rates of 0.5-0.8 °C/h. Spinel chemistry suggests that crystallization took place under one of the most reduced conditions for martian meteorites, at an f O2 3 log units below the quartz-fayalite-magnetite (QFM) buffer. The olivine megacrysts are heterogeneously distributed in the rock. Crystal size distribution analysis suggests that they constitute a population formed under steady-state conditions of nucleation and growth, although a few grains may be cumulates. The parent melt is thought to have been derived from partial melting of a light rare earth element- and platinum group element-depleted mantle source. Shergottites, EETA79001 lithology A, DaG 476/489, and Dhofar 019, although of different ages, comprise a particular type of martian rocks. Such rocks could have formed from chemically similar source(s) and parent melt(s), with their bulk compositions affected by olivine accumulation.

Mineralogy, major element compositions of minerals, and elemental and oxygen isotopic compositions of the whole rock attest to a lunar origin of the meteorite Northwest Africa 032 (NWA 032), an unbrecciated basalt found in October 1999. The rock consists predominantly of olivine, pyroxene and chromite phenocrysts, set in a crystalline groundmass of feldspar, pyroxene, ilmenite, troilite and trace metal. Whole-rock shock veins comprise a minor, but ubiquitous portion of the rock. Undulatory to mosaic extinction in olivine and pyroxene phenocrysts and micro-faults in groundmass and phenocrysts also are attributed to shock. Several geochemical signatures taken together indicate unambiguously that NWA 032 originated from the Moon. The most diagnostic criteria include whole-rock oxygen isotopic composition and ratios of Fe:Mn in the whole rock, olivine, and pyroxene. A lunar origin is documented further by the presence of Fe-metal, troilite, and ilmenite; zoning to extremely Fe-rich compositions in pyroxene; the ferrous oxidation state of all Fe in pyroxene; and the rare-earth element pattern with a well-defined negative europium anomaly. This rock is similar in major element chemistry to basalts from Apollo 12 and 15, but is enriched in light rare-earth elements and has an unusually high Th/Sm ratio. Some Apollo 14 basalts yield a closer match to NWA 032 in rare-earth element patterns, but have higher concentrations of Al2O3. Ar-Ar step release results are complex, but yield a whole-rock age of ca. 2.8 Ga, suggesting that NWA 032 was extruded at 2.8 Ga or earlier. This rock may be the youngest sample of mare basalt collected to date. Noble gas concentrations combined with previously collected radionuclide data indicate that the meteorite exposure history is distinct from currently recognized lunar meteorites. In short, the geochemical and petrographic features of NWA 032 are not matched by Apollo or Luna samples, nor by previously identified lunar meteorites, indicating that it originates from a previously unsampled mare deposit. Detailed assessment of petrographic features, olivine zoning, and thermodynamic modelling indicate a relatively simple cooling and crystallization history for NWA 032. Chromite-spinel, olivine, and pyroxene crystallized as phenocrysts while the magma cooled no faster than 2 °C/hr based on the polyhedral morphology of olivine. Comparison of olivine size with crystal growth rates and preserved Fe-Mg diffusion profiles in olivine phenocrysts suggest that olivine was immersed in the melt for no more than 40 days. Plumose textures in groundmass pyroxene, feldspar, and ilmenite, and Fe-rich rims on the phenocrysts formed during rapid crystallization (cooling rates ~ 20 to 60 °C/hr) after eruption.

A new grouplet of primitive, metal-rich chondrites, here called the CB (C, carbonaceous; B, bencubbinite) chondrites, has been recognized. It includes Bencubbin, Weatherford, Hammadah a1 Hamra (HH) 237 and Queen Alexandra Range (QUE) 94411, paired with QUE 94627. Their mineral compositions, as well as their oxygen and nitrogen isotopic compositions, indicate that they are closely related to the CR and CH chondrites, all of which are members of the more inclusive CR clan. CB chondrites have much greater metal/silicate ratios than any other chondrite group, widely increasing the range of metal/silicate fractionation recorded in solar nebular processes. They also have the greatest moderately volatile lithophile element depletions of any chondritic materials. Metal has compositional trends and zoning patterns that suggest a primitive condensation origin, in contrast with metal from other chondrite groups. CB chondrites, as well as other CR clan chondrites, have much heavier nitrogen (higher 15N/14N) than that in other chondrite groups. The primitive characteristics of the CB chondrites suggest that they contain one of the best records of early nebular processes. Another chondrite, Grosvenor Mountains 9555 1, is petrographically similar to the CB chondrites, but its mineral and oxygen and nitrogen isotope compositions indicate that it formed from a different nebular reservoir.

A synthetic material with solar elemental proportions of iron, magnesium, silicon, titanium, calcium, and aluminum oxides and doped with rare earth elements was evaporated in a vacuum furnace at 1800 and 2000°C for different durations to study its chemical and isotopic evolution during the evaporation process. It is demonstrated that kinetic evaporation of solar composition material can produce residues of calcium-, aluminum-rich inclusion bulk chemistry. The evaporation sequence of the main constituents in this solar composition material is iron > silicon ≈ magnesium > titanium. Calcium and aluminum remain unevaporated after evaporation of 95% of the solar composition material. The chemical fractionation between the gas and condensed phase is a function not only of temperature and pressure, but also of the bulk chemical composition of the condensed phase. During the evaporation process, cerium is almost as volatile as iron. The 2,000-fold cerium depletion found in some refractory inclusions in carbonaceous chondrites was reproduced in the evaporation experiment and can be readily explained as a result of evaporation of preexisting meteoritic material. Kinetic isotopic fractionation of magnesium, oxygen, and silicon follows the Rayleigh distillation law during the laboratory evaporation of synthetic solar composition material. This implies that the residue is well mixed during the evaporation process and that the evaporation kinetic processes (both chemical and isotopic) are surface reaction-controlled. The isotopic mass fractionation factors are lower than those predicted from theoretical calculations by using the square root of mass ratios of likely evaporating species. Thus, the surface reaction is more complicated than decomposition into single gas species of each element.

Los Angeles is a new martian meteorite that expands the compositional range of basaltic shergottites. Compared to Shergotty, Zagami, QUE94201, and EET79001-B, Los Angeles is more differentiated, with higher concentrations of incompatible elements (e.g., La) and a higher abundance of late-stage phases such as phosphates and K-rich feldspathic glass. The pyroxene crystallization trend starts at compositions more ferroan than in other martian basaits. Trace elements indicate a greater similarity to Shergotty and Zagami than to QUE94201 or EET79001-B, but the Mg/Fe ratio is low even compared to postulated parent melts of Shergotty and Zagami. Pyroxene in Los Angeles has 0.7-4-microns-thick exsolution lamellae, approx. 10 times thicker than those in Shergotty and Zaganii. Opaque oxide compositions suggest a low equilibration temperature at an oxygen fugacity near the fayafite-magnetitequartz buffer. Los Angeles cooled more slowly than Shergotty and Zagami. Slow cooling, coupled with the ferroan bulk composition, produced abundant fine-grained intergrowths of fayalite, hedenbergite, and silica, by the breakdown of pyroxferroite. Shock effects in Los Angeles include maskelynitized plagioclase, pyroxene with mosaic extinction, and rare fault zones. One such fault ruptured a previously decomposed zone of pyroxferroite. Although highly differentiated, the bulk composition of Los Angeles is not close to the low-Ca/Si composition or the globally wind-stirred soil of Mars.

— Two pallasites, Vermillion and Yamato (Y)-8451, have been studied to obtain petrologic, trace element, and O-isotopic data. Both meteorites contain low-Ca and high-Ca pyroxenes (

The carbonaceous chondrites display the widest range of oxygen isotopic composition of any meteorite group, as a consequence of the interaction of primordial isotopic reservoirs in the solar nebula. These isotopic variations can be used to identify the reservoirs and to determine conditions and loci of their interactions. We present a comprehensive set of whole-rock analyses of CV, CO, CK, CM, CR, CH, and CI chondrites, as well as selected components of some of these meteorites. A simple model is developed which describes the isotopic behavior during parent-body aqueous alteration processes. The process of thermal dehydration also produces a recognizable effect in the oxygen isotopic composition.

— We studied the petrography, mineralogy, bulk chemical, I-Xe, and O-isotopic compositions of three dark inclusions (E39, E53, and E80) in the reduced CV3 chondrite Efremovka. They consist of chondrules, calcium-aluminum-rich inclusions (CAIs), and fine-grained matrix. Primary minerals in chondrules and CAIs are pseudomorphed to various degrees by a mixture largely composed of abundant (>95%), fine-grained (>0.2 μm) fayalitic olivine (Fa35–42) and minor amounts of chlorite, poorly-crystalline Si-Al-rich material, and chromite; chondrule and CAI shapes and textures are well-preserved. Secondary Ca-rich minerals (Ti-andradite, kirschsteinite, Fe-diopside) are common in chondrule pseudomorphs and matrices in E39 and E80. The degree of replacement increases from E53 to E39 to E80. Fayalitic olivines are heavily strained and contain abundant voids similar to those in incompletely dehydrated phyllosilicates in metamorphosed CM and CI chondrites. Opaque nodules in chondrules consist of Ni- and Co-rich taenite, Co-rich kamacite, and wairauite; sulfides are rare; magnetite is absent. Bulk O-isotopic compositions of E39 and E53 plot in the field of aqueously altered CM chondrites, close to the terrestrial fractionation line; the more heavily altered E39 is isotopically heavier than the less altered E53. The apparent I-Xe age of E53 is 5.4 Ma earlier than Bjurbole and 5.7 ± 2.0 Ma earlier than E39. The I-Xe data are consistent with the most heavily altered dark inclusion, E39 having experienced either longer or later alteration than E53. Bulk lithophile elements in E39 and E53 most closely match those of CO chondrites, except that Ca is depleted and K and As are enriched. Both inclusions are depleted in Se by factors of 3–5 compared to mean CO, CV, CR, or CK chondrites. Zinc in E39 is lower than the mean of any carbonaceous chondrite groups, but in E53 Zn is similar to the means in CO, CV, and CK chondrites. The Efremovka dark inclusions experienced various degrees of aqueous alteration, followed by low degree thermal metamorphism in an asteroidal environment. These processes resulted in preferential oxidation of Fe from opaque nodules and formation of Ni- and Co-rich metal, metasomatic alteration of primary minerals in chondrules and CAIs, and the formation of fayalitic olivine and secondary Ca-Fe-rich minerals. Based on the observed similarities of the alteration mineralization in the Efremovka and Allende dark inclusions, we infer that the latter may have experienced similar alteration processes.

— Lunar meteorite Dar al Gani 262 (DG 262)—found in the Libyan part of the Sahara—is a mature, anorthositic regolith breccia with highland affinities. The origin from the Moon is undoubtedly indicated by its bulk chemical composition; radionuclide concentrations; noble gas, N, and O isotopic compositions; and petrographic features. Dar al Gani 262 is a typical anorthositic highland breccia similar in mineralogy and chemical composition to Queen Alexandra Range (QUE) 93069. About 52 vol% of the studied thin sections of Dar al Gani 262 consist of fine-grained(100 μm) constituents, and 48 vol% is mineral and lithic clasts and impact-melt veins. The most abundant clast types are feldspathic fine-grained to microporphyritic crystalline melt breccias (50.2 vol%; includes recrystallized melt breccias), whereas mafic crystalline melt breccias are extremely rare (1.4 vol%). Granulitic lithologies are 12.8 vol%, intragranularly recrystallized anorthosites and cataclastic anorthosites are 8.8 and 8.2 vol%, respectively, and (devitrified) glasses are 2.7 vol%. Impact-melt veins (5.5 vol% of the whole thin sections) cutting across the entire thin section were probably formed subsequent to the lithification process of the bulk rock at pressures below 20 GPa, because the bulk rock never experienced a higher peak shock pressure. Mafic crystalline melt breccias are very rare in Dar al Gani 262 and are similar in abundance to those in QUE 93069. The extremely low abundance of mafic components and the bulk composition may constrain possible areas of the Moon from which the breccia was derived. The source area of Dar al Gani 262 must be a highland terrain lacking significant mafic impact melts or mare components. On the basis of radionuclide activities, an irradiation position of DG 262 on the Moon at a depth of 55–85 g/cm3and a maximum transit time to Earth

Oxygen isotope analyses have been obtained for magnetite and diopside from mafic alkaline volcanic rocks of kamafugitic affinities from Brazil. These rocks are part of the Alto do Paranaiba and Santo Antonio volcanic provinces of Cretaceous age. Based on the clinopyroxene–magnetite pair, the isotopic temperatures obtained for the rocks of the two provinces are: mafitites −1140–920°C; leucitites −920–830°C; kalsilitites −820°C; analcimites (originally leucitites) −1060–1050°C; cumulate pyroxenites 750–690°C. The Mata da Corda (Alto Paranaiba Province) and Santo Antonio da Barra range in δ 18 O coincides with typical values for mantle-derived magmas.

We have characterized the most phyllosilicate-rich members of the CM chondrite group. Based upon petrographic and compositional factors, we conclude that these particular meteorites have experienced pervasive aqueous alteration far beyond that witnessed by typical CMs. The lack of anhydrous silicates, CAI and (except as relicts) chondrules merits the classification of type CMI for three meteorites (EET 83334, ALH 88045, and one Kaidun lithology). Still other CMs, notably ALH 83100, EET 90047, and Yamato 82042, are clearly intermediate between types 1 and 2. Brecciated CM chondrites like Cold Bokkeveld contain all of these varied lithologies. The CM chondrites thus exhibit the complete petrologic range from 2 through 1. Our results show that progressive aqueous alteration on the parent CM asteroid(s) was, locally, accompanied by significant increases in temperature (to a peak of ∼450°C for the Kaidun lithology), fO2, and (locally) degree of chemical leaching, all well beyond the conditions recorded by typical CM2s. The most altered CMs also are commonly deformed, displaying a distinct lineation probably due to static rather than dynamic forces.

We have conducted petrologic, chemical, and isotopic studies of lodranites in an attempt to constrain their genesis. Lodran, Gibson, Y-791491, Y-791493, Y-74357, Y-8002, Y-75274, MAC 88177, LEW 88280, EET 84302, FRO 90011, and QUE 93148 are classified as lodranites. Lodranites and acapulcoites are indistinguishable on the basis of oxygen isotopic compositions but are distinct in average grain sizes of their mafic silicates, with lodranites being significantly coarser-grained. Lodranites exhibit a diverse range of petrologic and mineralogic features: they range widely in mafic silicate compositions (Fa3–13), plagioclase (0–11.4 vol%), Fe,Ni metal (0.5–20 vol%), and troilite (0.2–5.3 vol%) contents; and shock levels (S1–S4) . They appear to have experienced high peak temperatures and rapid cooling in the temperature range recorded by metallographic cooling rates (i.e., 700-350°C). The only dated lodranite, Gibson, cooled to Ar closure temperatures at 4.49 ± 0.01 Ga. Lodranites formed from chemically and isotopically heterogeneous precursors in which the mineral and oxygen isotopic compositions were correlated. Heating of their parent body to temperatures between ∼ 1050–1200°C resulted in formation of Fe,NiFeS and basaltic partial melts. Depletions of troilite and/ or plagioclase in most lodranites testify to the removal of some of these partial melts, although melt migration was complex. Lodranites appear to have experienced a complex cooling history of slow cooling at high temperatures, followed by rapid cooling at intermediate temperatures, possibly related to breakup of the parent body. Lodranites were liberated from their parent body during 1–3 impact events, with most having cosmic ray exposure ages of 5.5–7 Ma. The acapulcoites are samples from the same parent body but were heated to lower temperatures and, thus, experienced lower degrees of partial melting.

Diamond-bearing eclogites are an important component of the xenoliths that occur in the Mir kimberlite, Siberian platform, Russia. We have studied 16 of these eclogite xenoliths, which are characterized by coarse-grained, equigranular garnet and omphacite. On the basis of compositional variations in garnet and clinopyroxene, this suite of eclogites can be divided into at least two groups: a high-Ca group and a low-Ca group. The high-Ca group consists of high-Ca garnets in equilibrium with pyroxenes that have high Ca-ratios [Ca/(Ca+Fe+Mg)] and high jadeite contents. These high-Ca group samples have high modal% garnet, and garnet grains often are zoned. Garnet patches along rims and along amphibole- and phlogopite-filled veins have higher Mg and lower Ca contents compared to homogeneous cores. The low-Ca group consists of eclogites with low-Ca garnets in equilibrium with pyroxenes with a low Ca-ratio, but variable jadeite contents. These low-Ca group samples typically have low modal% of garnet, and garnets are rarely compositionally zoned. Three samples have mineralogic compositions and modes transitional to the high- and low-Ca groups. We have arbitrarily designated these samples as the intermediate-Ca group. The rare-earth-element (REE) contents of garnet and clinopyroxene have been determined by ion microprobe. Garnets from the low-Ca group have low LREE contents and typically have [Dy/Yb]n 1. Garnets from the intermediate-Ca group have REE contents between the high- and low-Ca groups. Clinopyroxenes from the low-Ca group have convex-upward REE patterns with relatively high REE contents (ten times chondrite), whereas those from the high-Ca group have similar convex-upward shapes, but lower REE contents, approximately chondritic. Reconstructed bulk-rock REE patterns for the low-Ca group eclogites are relatively flat at approximately ten times chondrite. In contrast, the high-Ca group samples typically have LREE-depleted patterns and lower REE contents. The δ18O values measured for garnet separates range from 7.2 to 3.1‰. Although there is a broad overlap of δ18O between the low-Ca and high-Ca groups, the low-Ca group samples range from mantle-like to high δ18O values (4.9 to 7.2‰), and the high-Ca group garnets range from mantle-like to low δ18O values (5.3 to 3.1‰). The oxygen isotopic compositions of two of the five high-Ca group samples and four of the eight low-Ca group eclogites are consistent with seawater alteration of basaltic crust, with the low-Ca group eclogites representative of low-temperature alteration, and the high-Ca group samples representative of high-temperature hydrothermal seawater alteration. We interpret the differences between the low- and high-Ca group samples to be primarily a result of differences in the protoliths of these samples. The high-Ca group eclogites are interpreted to have protoliths similar to the mid to lower sections of an ophiolite complex. This section of oceanic crust would be dominated by rocks which have a significant cumulate component and would have experienced high-temperature seawater alteration. Such cumulate rocks probably would be LREE-depleted, and can be Ca-rich because of plagioclase or clinopyroxene accumulation. The protoliths of the low-Ca group eclogites are interpreted to be the upper section of an ophiolite complex. This section of oceanic crust would consist mainly of extrusive basalts that would have been altered by seawater at low temperatures. These basaltic lavas would probably have relatively flat REE patterns, as seen for the low-Ca group eclogites.

The Kakangari, LEW 87232, and Lea Co. 002 chondrites have a similar set of petrologic and oxygen isotopic characteristics that distinguishes them from other chondrite groups. They are here established to constitute a single chondrite grouplet—the K (after Kakangari) chondrites. The K chondrites have (1) high matrix abundances (33–77 vol%) as do carbonaceous chondrites, (2) metal abundances (6–10 vol%) that are similar to the H group ordinary chondrites, (3) average mafic silicate compositions (average Kakangari olivine = Fa2.2; enstatite Fs4.4) that indicate an oxidation state intermediate between H and E chondrites, (4) matrix that differs from that in other chondrite groups in being enstatite-rich with compositions more Mg-rich (average = Fs3) than those in the chondrules, (5) refractory lithophile element abundances (

— The Mbosi iron meteorite contains millimeter size silicate inclusions. Mbosi is an ungrouped iron meteorite with a Ge/Ga ratio >10, which is an anomalous property shared with the five-member IIF iron group, the Eagle Station pallasites and four other ungrouped irons. Neither the IIF group nor the four other ungrouped irons are known to have silicate inclusions. Chips from three Mbosi inclusions were studied, but most of the work concentrated on a whole 3.1 mm circular inclusion. This inclusion consists of a mantle and a central core of different mineralogies. The mantle is partially devitrified quartz-normative glass, consisting of microscopic crystallites of two pyroxenes and plagioclase, which are crystalline enough to give an x-ray powder diffraction pattern but not coarse enough to permit analyses of individual minerals. The core consists of silica. The bulk composition does not match any known meteorite type, although there is a similarity in mode of occurrence to quartz-normative silicate inclusions in some HE irons. Mbosi silicate appears to be unique. The bulk rare earth element (REE) pattern of the mantle is flat at ≅ 7×C1; the core is depleted in REE but shows a small positive Eu anomaly. The O-isotope composition of bulk silicate lies on a unit slope mixing line (parallel and close to the C3 mixing line) that includes the Eagle Station pallasites and the iron Bocaiuva (related to the IIF irons); all of these share the property of having Ge/Ga ratios >10. It is concluded that Mbosi silicate represents a silica-bearing source rock that was melted and injected into metal. Melting occurred early in the history of the parent body because the metal now shows a normal Widmanstatten structure with only minor distortion that was caused when the parent body broke up and released meteorites into interplanetary space. The cause of Ge/Ga ratios being >10 in these irons is unknown. The fact that silicates in Mbosi, Bocaiuva (related to IIF irons) and the Eagle Station trio of pallasites, all characterized by a Ge/Ga ratio >10, lie on a unit slope mixing line in the O-isotope diagram suggests that their origins are closely related. The C3 chondrites appear to be likely precursors for silicates in Mbosi, Bocaiuva and the Eagle Station pallasites.

We have conducted petrologic, chemical, and isotopic studies of acapulcoites (Acapulco, Monument Draw, Yamato 74063, ALH A77081, ALH A81261, ALH A81315, ALH 78230, ALH A81187 and ALH 84190) in an attempt to constrain their genesis. Acapulcoites have distinctly different oxygen isotopic compositions than silicate inclusions in IAB and IIICD irons, winonaites and ureilites and, thus, formed on a different parent body. Oxygen isotopic compositions, which are slightly heterogeneous within the group, overlap with lodranites, indicating a likely origin on a common parent body. These groups can be distinguished on the basis of mafic silicate grain size. All acapulcoites have mafic silicate compositions intermediate between E and H chondrites, roughly chondritic mineralogies, achondritic, equigranular textures, micrometer to centimeter sized veins of Fe,NiFeS which cross-cut silicate phases, rapid metallographic cooling rates at ∼600−400°C (103–105°C/Myr) and trapped noble gas abundances comparable to type 3–4 ordinary chondrites. They exhibit variable mafic silicate zoning, abundance of Fe,NiFeS veins, REE abundances and patterns and, possibly, cosmic ray exposure ages (∼5–7 Ma). Momument Draw and Yamato 74063 retain rare relict chondrules. Phosphates are associated with Fe,NiFeS veins or form separate veins in Monument Draw and Acapulco. Heating and cooling of acapulcoites occurred very early in the history of the Solar System, as evidenced by the 39Ar40Ar ages of ∼4.51 Ga. These ages appear distinctly younger than the likely formation time for Acapulco of 4.557 Ga, but are older than analogous 39Ar40Ar ages for most chondrites. Acapulcoites formed from a precursor chondrite which differs from known chondrites in mineral and oxygen isotopic compositions. Heating to ∼950–1000°C resulted in melting at the Fe,NiFeS cotectic, but silicates did not melt. Silicate textures resulted from extensive solid-state recrystallization. Heating was by noncollisional sources (e.g., 26Al, electromagnetic induction). Despite uncertainties owing to a lack of data, acapulcoites may have experienced a three-stage thermal history of slow cooling at high temperature, rapid cooling at intermediate temperatures, and slow cooling at low temperatures, possibly resulting from breakup and gravitational reassembly of the parent body. The complex thermal history is also reflected in disequilibrium REE abundances. One or at most two impact events (∼7 Ma and possibly ∼5 Ma ago) are consistent with the cosmic ray exposure ages of all four acapulcoites for which cosmogenic noble gas data exist.

Oxygen isotope fractionations in laboratory systems have been determined for each of the following minerals relative to calcite: muscovite, phlogopite, fluorophlogopite, and rutile. Statistical mechanical calculations following the method of Kieffer (1982) were fit to the experimental data and then used to extrapolate the experimental results to higher and lower temperatures. The calculations are represented by a series of equations which allow the reduced partition function ratios (β factors) for each of these minerals to be calculated at T > 400 K. These equations can be combined with corresponding equations for calcite, quartz, albite, anorthite, diopside, forsterite, and magnetite (Clayton and Kieffer, 1991) to give a large number of mineral-pair fractionations for use as isotopic thermometers. It was found that the high-frequency vibrations of OH bonds contribute such a small amount of the fractionation factors that they do not introduce significant nonlinearity to plots of Δ vs. T−2. The commonly used calibrations of quartz-muscovite and quartz-biotite fractionations are not in good agreement with the present experimental measurements. This probably reflects disturbance of the rock assemblages on which those calibrations were based, as a consequence of the high diffusivity of oxygen in micas. The experimental quartz-rutile fractionations are in good agreement with some earlier hydrothermal experiments and with an empirically determined calibration. The calculated rutile partition functions of Kieffer (1982) are not consistent with the experimental results, probably due in part to the neglect of the effect of cation mass on the vibrational energies. The large number of mineral systems with measured fractionation factors allows a test of various empirical relationships based on oxygen bond strengths. In general, these relationships are successful for anhydrous silicates, but do not adequately account for the behavior of hydrous minerals or metal oxides.

Oxygen isotope abundances provide a powerful tool for recognizing genetic relationships among meteorites. Among the differentiated achondrites, three isotopic groups are recognized: (l ) SNC (Mars), (2) Earth and Moon, and (3) HED (howardites, eucrites, diogenites). The HED group also contains the mesosiderites, main-group pallasites, and silicates from IIIAB irons. The angrites may be marginally resolvable from the HED group. Within each of these groups, internal geologic processes give rise to isotopic variations along a slope- 1 2 fractionation line, as is well known for terrestrial materials. Variations of Δ17O from one planet to another are inherited from the inhomogeneities in the solar nebula, as illustrated by the isotopic compositions of chondrites and their constituents. Among the undifferentiated achondrites, five isotopic groups are found: (1) aubrites, (2) winonaites and IAB-IIICD irons, (3) brachinites, (4) acapulcoites and lodranites, and (5) ureilites. The isotopic compositions of aubrites coincide with the Earth and Moon, and also with the enstatite chondrites. These bodies apparently were derived from a. common reservoir, the isotopic composition of which was established at the chondrule scale by nebular processes. Isotopic similarities between chondrites and achondrites are seen only for the following instances: (1) enstatite chondrites and aubrites, (2) H chondrites and HE irons, and (3) L or LL chondrites and IVA irons. The isotopic data also support the following genetic associations: (1) winonaites and IAB-IIICD irons, (2) acapulcoites and lodranites, and (3) ureilites and dark inclusions of C3 chondrites. An attempt to reconcile the whole-planet isotopic compositions of Earth, Mars, and the eucrite parent body with mixing models of their chemical compositions failed. It is not possible to satisfy both the chemical and isotopic compositions of the terrestrial planets using known primitive Solar System components.

Data are presented for the O isotopic composition of clinopyroxene and garnet, the C isotopic composition of diamond, and the OH- content of garnet from eclogite xenoliths brought to the surface by the Udachnaya kimberlite pipe, Yakutia, Siberia. Radiogenic isotopic data suggest that the eclogites could have been derived from an ultradepleted mantle at approximately 2.9 Ga (Pearson et al., 1995; Snyder et al., in preparation). O isotopic compositions generally show equilibration between the eclogitic minerals (Δ_(cpx-Grt) = 0.11-0.41‰) and have δ^(18)O_(SMOW) for both garnet and clinopyroxene that lie near the range of accepted mantle values of 5.7±0.7‰. However, several eclogites indicate significant deviations from this range, at higher values of 6.8-7.0‰. Also, two eclogites lie at the lower end of the mantle range, at values of 4.8 and 5.0‰ (all in clinopyroxene). C isotopic compositions of diamonds all have δ^(13)C_(PDB) in the range of -1 to -7‰ and are centered at approximately -5‰, also within the range of accepted mantle values. The OH- contents of the garnet are generally between 0 and 22 ppm (as H_(2)0), although two samples exceed 70 ppm. This range of OH- is similar to eclogitic garnet from the Kaapvaal craton of southern Africa. The mantle C isotopic values of associated diamonds, the majority of O isotopic data, and the low OH- content of the minerals, although suggesting a general lack of crustal participation in the formation of the Udachnaya eclogites, do not rule out the participation of some ancient crustal material. That these eclogites include both ^(18)O-enriched and ^(18)O-depleted types suggests that the protoliths may have been overprinted by both low- and high-temperature hydrothermal events (cf. Jacob et aI., 1994). A positive correlation between δ^(18)O and ^(87)Sr/^(86)Sr allows the interpretation of these eclogites as representing a cross section of an Archean ophiolite. However, the lack of a single coherent grouping on a plot of δ^(18)O vs. ^(87)Sr/^(86)Sr suggests that, if the Udachnaya eclogites were derived from oceanic crust, they cannot be cogenetic and must represent at least two separate ophiolite sequences. Conversely, if the eclogites are found to be cogenetic, then a totally different process affected their formation and a probable metasomatic mechanism was operative. Because of the total lack of correlation of δ^(18)O with other geochemical parameters, we find no compelling evidence that all eclogites are derived ultimately from oceanic crust.

Laboratory experiments have been conducted to determine rates and other details of the oxygen isotopic exchange process between meteoritic material and water vapor. The meteoritic samples were totally or partially melted, or completely unmelted. The furnace atmosphere consisted of water vapor and hydrogen, and was diluted with helium for some of the experiments. Both isothermal and flash heating experiments were performed. Extensive oxygen isotope exchange has been observed between chondrule analogue melt and surrounding dilute water vapor, such that 50% equilibration occurs in charges near their liquidus in five minutes or less. The principal rate-limiting mechanism of the exchange is diffusion within the melt. The initial exchange rate also depends on the partial pressure of water, which points to the effect of the surface exchange process. The kinetics of the surface reaction have not been determined due to the restrictions of our experimental configuration. The extent of exchange observed in short time isothermal runs and in flash heating runs suggests that much of the isotopic variability of natural chondrules can be produced during chondrule-forming events by the gas/melt isotopic exchange processes. However, due to the very low gas densities in the nebula, multiple melting events might be needed to produce the chondrules with highly exchanged isotopic compositions. For a partially melted sample, as is often the case in natural chondrules, the rate of isotopic change of the bulk sample is determined by the exchange rates of both the melt and unmelted relict minerals. If the melt and relict minerals have a large difference in isotopic compositions, the exchange trajectory becomes markedly nonlinear. These observations are consistent with the observed dependence of extent of exchange in natural chondrules on the degree of melting, and imply that for each of the linear trends on the three-isotope diagram observed for natural chondrules, only two initial isotopic reservoirs might have existed.

The (1) CR chondrites, (2) LEW 85332,(3) Acfer 182,(4) ALH 85085-like chondrites, and (5) Bencubbin-like chondritic breccias are five kinds of chondritic groups which have dramatically different petrographic characteristics, but have mineralogical, bulk chemical, and oxygen and nitrogen isotopic similarities that indicate they are closely related. They are all considered to be members of what we term the CR chondrite clan. Distinguishing characteristics of CR clan chondrites include : (a) reduced, Mg-rich mafic silicates, (b) hydrous matrix and/or dark inclusions (except for Bencubbin-like chondrites), (c) high modal abundances of FeNi metal, (d) FeNi metal having a solar Ni : Co ratio, (e) solar (CI) abundances of refractory and moderately volatile lithophiles, and highly depleted abundances of volatile lithophiles, (f) similar oxygen isotopic compositions of whole rocks, chondrules and matrices, which are on or near the CR mixing line, and (g) anomalously high ^N abundances. CR clan chondrites must have formed in the same local region of the nebula, from closely related reservoirs of materials. The coexistence of anhydrous chondrules with hydrous matrix (and dark inclusions) in the LEW 85332,Acfer 182,and ALH 85085-like chondrites, as well as the widely differing degrees of hydration within and between chondritic samples, implies that hydration of the components was not variable in a single locality, but took place at a variety of locales prior to final lithification of the CR clan chondrites.

A large (greater than 4.5 x 7 x 4 mm), igneous-textured clast in the Bovedy (L3) chondrite is notable for its high bulk SiO2 content (is approximately equal to 57.5 wt%). The clast consists of normally zoned orthopyroxene (83.8 vol%), tridymite (6.2%), an intergrowth of feldspar (5.8%) and sodic glass (3.1%), pigeonite (1.0%), and small amounts of chromite (0.2%), augite, and Fe,Ni-metal; it is best described as a silica-rich orthopyroxenite. The oxygen-isotopic composition of the clast is similar, but not identical, to Bovedy and other ordinary chondrites. The clast has a superchondritic Si/Mg ratio, but has Mg/(Mg + Fe) and Fe/Mn ratios that are similar to ordinary chondrite silicate. The closest chemical analogues to the clast are radial-pyroxene chondrules, diogenites, pyroxene-silica objects in ordinary chondrites, and silicates in the IIE iron meteorite Weekeroo Station. The clast crystallized from a siliceous melt that cooled fast enough to prevent complete attainment of equilibrium but slow enough to allow nearly complete crystallization. The texture, form, size and composition of the clast suggestion that it is an igneous differentiate from an asteroid or planetesimal that formed in the vicinity of ordinary chondrites. The melt probably cooled in the near-surface region of the parent object. It appears that in the source region of the clast, metallic and silicate partial melt were largely-to-completely lost during a relatively low degree of melting, and that during a higher degree of melting, olivine and low-Ca pyroxene separated from the remaining liquid, which ultimately solidified to form the clast. While these fractionation steps could not have all occurred at the same temperature, they could have been accomplished in a single melting episode, possibly as a result of heating by radionuclides or by electromagnetic induction. Fractionated magmas can also account for other Si-rich objects in chondrites.

Oxygen isotopic compositions have been determined for whole-rock and separated components from the CI chondrites Alais, Ivuna, and Orgueil, and from the atypical CM chondrites Bells and Essebi. The composition of CI matrix is in agreement with previous measurements and is systematically different from that of CM matrix, probably due to warmer and wetter conditions of aqueous alteration for CI matrix. Although Bells matrix is like that of other CM chondrites, the matrix of Essebi falls in the CI field. Essebi also contains abundant magnetite, like CIs and unlike other CMs. The isotopic compositions of magnetite in Alais, Ivuna, Orgueil and Essebi define a trend with Δ17O of +1.3 to +1.8, distinctly out of isotopic equilibrium with the phyllosilicates in each meteorite. The magnetite serves as an isotopic tracer for the fluid which brought about aqueous alteration and oxidation, and thus provides additional evidence for a gaseous reservoir in the solar nebula which was more 16O-depleted than the earth.

— Previously, three meteorites from Australia and Antarctica were described as a new chondritic “grouplet” (Carlisle Lakes, Allan Hills (ALH) 85151, Yamato (Y) −75302; Rubin and Kallemeyn, 1989). This grouplet was classified as the “Carlisle Lakes-type” chondrites (Weisberg et al., 1991). Recently, one Saharan sample and four more Antarctic meteorites were identified to belong to this group (Acfer 217, Y-793575, Y-82002, PCA91002, PCA91241). The latter two are probably paired. With the meteorite Rumuruti, the first fall of this type of chondrite is known (Schulze et al., 1994). We report here on the Saharan meteorite Acfer 217 which has chemical and mineralogical properties very similar to Rumuruti and Carlisle Lakes. All eight members of this group, Rumuruti, Carlisle Lakes, ALH85151, Y-75302, Y-793575, Y-82002, Acfer 217, and the paired samples PCA91002 and PCA91241 justify the introduction of a new group of chondritic meteorites, the Rumuruti meteorites (R). Acfer 217 is a regolith breccia consisting of up to cm-sized clasts (∼33 vol%) embedded in a fine-grained, well-lithified clastic matrix. The most abundant mineral is olivine (∼72 vol%), which has a high Fa-content of 37–39 mol%. The major minerals (olivine, low-Ca pyroxene, Ca-pyroxene, and plagioclase) show some compositional variability indicating a slightly unequilibrated nature of the meteorite. Considering the mean olivine composition of Fa37.8 ± 5.7, a classification of Acfer 217 as a R3.8 chondrite would result; however, Acfer 217 is a regolith breccia consisting of clasts of various petrologic types. Therefore, we suggest to classify Acfer 217 as a R3–5 chondrite regolith breccia. The bulk meteorite is very weakly shocked (S2). The bulk composition of Acfer 217 and other R-meteorites show that the R-meteorites are basically chondritic in composition. The pattern of moderately volatile elements is unique in R chondrites; Na and Mn are essentially undepleted, similar to ordinary chondrites, while Zn and Se contents are similar to concentrations in CM chondrites. The oxygen isotopic composition in Acfer 217 is similar to that of Rumuruti, Carlisle Lakes, ALH 85151, and Y-75302. In a δ17O vs. δ18O-diagram, the R-meteorites form a group well resolved from other chondrite groups. Acfer 217 was a meteoroid of common size with a radius between 15–65 cm and with a single stage exposure history. Based on 21Ne, an exposure age of about 35 Ma was calculated.

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 IIE 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 IIE iron. Whole rock Watson silicate shows an enrichment in K and P (each approximately 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 (Fs9Wo14)(with very fine exsolution lamellae), antiperthite feldspar (An1-3Or5) with less than 1 micron exsolution lamellae (An1-3Or greater than 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 approximately 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.

Igneous inclusions and hosts of the Yamato ordinary chondrites Y-75097 (L6), Y-793241 (L6) and Y-794046 (H5) were analyzed for lithophile trace elements, and Rb-Sr, rare gas and oxygen isotopes, together with preliminary petrographic examinations. On a three oxygen-isotope plot, all the inclusions lie near the H-chondrite field. The Y-75097 host and inclusion were severely shocked and the Rb-Sr systematics were disturbed by a 500Ma event which was defined by the K-Ar age. The Y-793241 host and inclusion are unshocked and have an old K-Ar age of 4270±170Ma and undisturbed Rb-Sr systematics for the bulk meteorite. Both Y-75097 and Y-793241 inclusions have similar chemical compositions and mineral assemblages consisting mainly of olivine (Fa_), and minor plagioclase (An_), chlor-apatite, merrillite and chromite. Olivines in both inclusions equilibrated with those of their L6 hosts. The two inclusion mantles consisting of mainly olivine and plagioclase show a highly fractionated REE pattern with middle REE depletion and a large positive Eu anomaly (50-100 times chondritic) (V-shaped). A model calculation suggests that this remarkable REE fractionation was produced by thermal equilibration with the phosphate-rich cores of inclusions during the igneous formation and the metamorphic event. The Y-794046 inclusion comprises abundant anhedral olivines (Fa_), fractured pyroxenes (Fs_) and microcrystalline plagioclase (An_Ab_Or_). The inclusion did not equilibrate with its host which has less Fe-rich olivines (Fa_) and more Fe in pyroxenes (Fs_). The inclusion shows an unfractionated REE pattern. We suggest that the three inclusions formed by melting of differentiated precursor materials carrying unfractionated REE. They were then incorporated into the L-or H-chondrite parent bodies and subjected to the early thermal metamorphism, which eventually overprinted the fractionated REE in the Y-75097 and Y-793241 inclusions by solid/solid equilibrium partitioning. The Y-794046 inclusion was subjected to less extensive equilibration, so that REE abundances remained unfractionated.

The Divnoe meteorite is an olivine-rich primitive achondrite with subchondritic chemistry and mineralogy. It has a granoblastic, coarse-grained, olivine groundmass (CGL: coarse-grained lithology) with relatively large pyroxene-plagioclase poiklitic patches (PP) and small fine-grained domains of an opaque-rich lithology (ORL). Both PP and ORL are inhomogeneously distributed and display reaction boundaries with the groundmass. Major silicates, olivine Fa(20-28) and orthopyroxyene Fs(20-28 Wo(0.5-2.5), display systematic differences in composition between CGL and ORL as well as a complicated pattern of variations within CGL. Accessory plagioclase has low K content and displays regular igneous zoning with core compositions An(40-45) and rims An(32-37). The bulk chemical composition of Divnoe is similar to that of olivine-rich primitive achondrites, except for a depletion of incompatible elements and minor enrichment of refractory siderophiles. Oxygen isotope compositions for whole-rock and separated minerals from Divnoe fall in a narrow range, with mean delta O-18 = +4.91, delta O-17 = +2.24, and Delta O-17 = -0.26 +/- 0.11. The isotopic composition is not within the range of any previously recognized group but is very close to that of the brachinites. To understand the origin of Divnoe lithologies, partial melting and crystallization were modelled using starting compositions equal to that of Divnoe and some chondritic meteorites. It was found that the Divnoe composition could be derived from a chondritic source region by approximately 20 wt% partial melting at Ta approximately 1300 C and log(fO2) = IW-1.8, followed by approximtely 60 wt% crystallization of the partial melt formed, and removal of the still-liquid portion of the partial melt. Removal of the last partial melt resulted in depletion of the Divnoe plagioclase in Na and K. In this scenario, CGL represents the residue of partial melting, and PP is a portion of the partial melt that crystallized in situ. The ORL was formed during the final stages of partial melting by reaction between gaseous sulfur and residual olivine in the source region. A prominent feature of Divnoe is fine micron-scale chemical variations within olivine grains, related to lamellar structures the olivines display. The origin of these structures is not known.

The ten specimens of the paired Acfer 059/El Djouf 001 CR2 chondrite contain abundant lithic fragments which we refer to as dark clasts. Petrological and mineralogical studies reveal that they are not related to the CR2 host meteorite but are similar to dark clasts in other CR2 chondrites. Dark clasts consist of chondrule and mineral fragments, phyllosilicate fragments and clusters, magnetite, sulfides and accessory phases, embedded into a very fine-grained, phyllosilicate-rich matrix. Magnetite has morphologies known from CI chondrites: spherules, framboids and platelets. Average abundances of major elements in the dark clasts are mostly in the range of both CR and CV chondrites, but strong depletions in Na and S are apparent. Oxygen isotopic compositions of two dark clasts suggest relationships to type 3 carbonaceous chondrites and dark inclusions in Allende. The dark clasts are clearly different in texture and mineralogical compositions from the host matrix of Acfer 059/El Djouf 001. Therefore, these dark clasts are xenoliths and are quite unlike the Acfer 059/El Djouf 001 CR2 host meteorite. We suggest that dark clasts accreted at the same time with all other components during the formation of Acfer 059/El Djouf 001 whole rock.

Eucrites are a class of basaltic meteorites that share common mineralogical, isotopic, and chemical properties and are thought to have been derived from the same parent body, possibly asteroid 4 Vesta. The texture, mineralogy, and noble gas data of the recently recovered meteorite, Northwest Africa (NWA) 011, are similar to those of basaltic eucrites. However, the oxygen isotopic composition of NWA011 is different from that of other eucrites, indicating that NWA011 may be derived from a different parent body. The presence of basaltic meteorites with variable oxygen isotopic composition suggests the occurrence of multiple basaltic meteorite parent bodies, perhaps similar to 4 Vesta, in the early solar system.

Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite delta C-13). Petrologic subtype 3.2 +/- 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most equilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.

A petrologic, geochemical, and oxygen isotropic study of the CR chondrites including Renazzo, Al Rais, El Djouf 001 and the paired Acfer meteorites, EET87770 and the paired samples, MAC87320, Y790112, Y793495, and Y791498 is presented. It is concluded that the CR group is characterized by abundant large multilayered, Fe, Ni metal-rich, type I chondrules; abundant matrix and dark inclusions; unique assemblages of serpentine and chlorite-rich phyllosilicates and Ca-carbonates; Ca-carbonate rims on chondrules; abundant Fe, Ni metal with a positive Ni vs. Co trend and a solar Ni:Co ratio; and amoeboid olivine aggregates with Mn-rich and Mn-poor forsterite.

Oxygen and carbon isotopic fractionation factors have been measured by direct exchange between carbon dioxide and calcite over the temperature range 400–950°C at pressures of 1–13 kilobars. Equilibrium constants for oxygen exchange are well determined from 400 to 800°C, and differ substantially from previous experimental and theoretical estimates. Carbon isotopic fractionations have larger uncertainties at all temperatures. Both oxygen and carbon isotopic fractionations are well reproduced by statistical mechanical calculations with simple treatment of the calcite lattice vibrations. A recalculated calcite-graphite fractionation curve based on new calculations of partition functions ratios for calcite suggests that this system is well suited for high-temperature isotopic thermometry of graphitic marbles as first proposed by Valley and O'Neil (1981). The rate of exchange of both oxygen and carbon between carbon dioxide and calcite is rapid, and proceeds by a combination of diffusion and minor recrystallization.

The petrogenesis of the Carlisle Lakes-type chondrites and their relationship to other chondrites are studied using new petrologic data, especially on mineralogical zoning patterns, and oxygen isotopic analyses of the whole chondrites and some of chondrules. Detailed zoning profiles of mafic silicates are measured in order to determine the environment(s) in which their oxidation states are established. It is concluded that the zoning did not form during crystallization from a melt droplet chondrule but post-dated chondrule formation. Parent-body thermal metamorphism and nebular gas-solid exchange reactions accompanied by condensation of new FeO-rich olivine, utilizing existing olivine surfaces as nucleation sites are considered as hypotheses explaining the zoning. The occurrence of zoned grains in a host that is mainly equilibrated suggests that the equilibration of the Carlisle Lakes-type chondrites occurred prior to final lithification.

Several stages in the evolution of ordinary chondritic meteorites are recorded in the oxygen isotopic composition of the meteorites and their separable components (chondrules, fragments, clasts, and matrix). The whole-rock isotopic compositions reflect the iron-group of the meteorite (H, L, or LL). Isotopic uniformity of H3 to H6 and L3 to L6 are consistent with closed-system metamorphism within each parent body. LL3 chondrites differ slightly from LL4 to LL6, implying a small degree of open-system aqueous alteration and carbon reduction. On the scale of individual chondrules, the meteorites are isotopically heterogeneous, allowing recognition of the solar-nebular processes of chondrule formation. Chondrules for all classes of ordinary chondrites are derived from a common population, which was separate from the population of chondrules in carbonaceous or enstatite chondrites. Chondrules define an isotopic mixing line dominated by exchange between (O - 16)-rich and (O - 16)-poor reservoirs. The oxygen isotopic compositions of chondrites serve as 'fingerprints' for identification of genetic association with other meteorite types (achondrites and iron) and for recognition of source materials in meteoritic breccias.

Results are presented on a detailed petrologic, chemical, and isotopic study of the so-called FUN inclusion (1623-5) from the Vigarano C3V chondrite. It is shown that the precursor material from which the Vigarano 1623-5 has formed contained some nuclear isotopic anomalies; this precursor was composed of melted and crystallized spinel, olivine, fassaite, and melilite. The results on the petrologic and isotopic properties of 1623-5 indicate unambiguously the action of volatilization in the evolution of this inclusion.

Synthetic forsterite (Mg2SiO4) was partially evaporated in vacuum for various durations and at different temperatures. The residual charges obtained when molten Mg2SiO4 was evaporated to 12 percent of its initial mass were enriched in heavy isotopes by about 20, 30, and 15 per mil/amu for O, Mg, and Si, respectively, whereas solid forsterite evaporated to a similar residual mass fraction showed negligible fractionations. These results imply that calcium and aluminum-rich refractory inclusions in carbonaceous chondrites must have been at least partially molten in the primordial solar nebula if the observed large mass fractionation effects were caused by evaporation processes in the nebula.

The Sr, Nd, and O isotopic compositions of garnet and clinopyroxene mineral separates from nine eclogite xenoliths from the Bellsbank kimberlite (erupted at 120 Ma) define three groups. Group A eclogites, considered to be mantle cumulates, are characterized by 6180, and 87Sr/Srsr values typical of mantle-derived materials (+5.1 to +5.6%o and 0.7042-0.7046, respectively), and very low Sm/Nd ratios, (apparent) Rb/Sr ratios and ~NaLlZ01 values (0.057-0.078, 0.00005-0.00136 and - 14 to - 16 respectively). The REE and isotopic data for these eclogites can be modelled in terms of crystallization from a Group II kimberlite magma at - 1-1.5 Ga. Group B and C eclogites, believed to be the metamorphosed products of ancient subducted oceanic crust, are characterized by low 3180 (+2.9 to +4.7), extremely high ~Nd[a20] (-- +40 to +219), and radiogenic 87Sr/S6Sr ratios (0.708-0.710). The Sm/Nd ratios of the Group B eclogites are very high (up to 1.6). The data for Group B and C eclogites define a linear correlation on Sm/Nd and 1/Nd vs. ~Nal~201 diagrams. These relationships are consistent with mixing of the Bellsbank kimberlite (CNO [1201 = --10; Sm/Nd = 0.10) with a depleted eclogite end-member (eNd[120 ] + 219; Sm/Nd = 1.6) during a cryptic metasomatic event. The Sr isotopic variations in Group B and C eclogites cannot be generated by simple two-component mixing. The St, Nd, and O isotope data for Group B and C eclogites probably reflect a complex sequence of depletion and enrichment events, in both crust and mantle settings. Enrichments which possibly affected the Group B and C eclogites include seawater-alteration of a MORB-like protolith, which lowered the 6180 and raised the SVSr/86Sr ratio, but left the Nd isotopic compositions unchanged, and cryptic metasomatism by the magmatism that produced the Bellsbank kimberlite. The high Sm/Nd ratio of the depleted eclogite end-member cannot be generated by extraction of a melt from a modern MORB composition. Rather, it is argued that such high Sm/Nd ratios are produced as a result of partitioning during the recrystallization of a MORB-like component to eclogite during subduction. Nd model ages suggest that this process occurred - 2.3-2.4 Ga.

The origin and the history of dark inclusions (DIs) are investigated using petrologic, chemical, and oxygen isotopic data on ten DI samples from Allende, Leoville, and Vigarano. These data indicate that the DIs of the Leoville and Vigarano are closely similar to those of Allende. The inclusions appear to be fragments of CV3 parent bodies which were processed to different degrees prior to their incorporation as clasts into the Allende, Leoville, and Vigarano chondrites. The processing homogenized the olivine compositions, presumably through heating, and also involved oxygen exchange with O-16-poorer surroundings.

The relationship between the porphyritic chondrules and coase-grained chondrule rims of the Allende CV chondrite are examined. The oxygen isotopic compositions of seven chondrule-rim pairs and a large rimless refractory chondrule from Allende are determined. The results suggest that, to account for the O-isotopic compositions of the CV chondrules and rims, three solid precursor components are required: a high-temperature, refractory-, alkali, and (O-16)-rich component; a low-temperature, FeO-rich, refractory, and (O-16)-poor component, and an additional component to explain the composition of BO chondrules.

The IIIA and IIIB iron meteorites are considered to have formed in the cores of asteroids. A silicate inclusion within the IIIA meteorite Puente del Zacate consisting of olivine (Fa 4 ), low-calcium pyroxene (Fs 6 Wo 1 ), chromium diopside (Fs 3 Wo 47 ), plagioclase (An 14 Or 4 ), graphite, troilite, chromite, daubreelite, and iron metal resembles inclusions in IAB iron meteorites. The oxygen isotopic composition of the Puente del Zacate inclusion is like chromite and phosphate inclusions in other IIIA and IIIB irons. The Puente del Zacate inclusion may have been derived from the lower mantle of the IIIAB parent asteroid.

The preatmospheric mass of the Tagish Lake meteoroid was about 200,000 kilograms. Its calculated orbit indicates affinity to the Apollo asteroids with a semimajor axis in the middle of the asteroid belt, consistent with a linkage to low-albedo C, D, and P type asteroids. The mineralogy, oxygen isotope, and bulk chemical composition of recovered samples of the Tagish Lake meteorite are intermediate between CM and CI meteorites. These data suggest that the Tagish Lake meteorite may be one of the most primitive solar system materials yet studied.

Weathering effects on meteorite finds from the Acfer region were studied by various analytical techniques and in dependence on the depth of sampling. In thin sections of weathered meteorites, weathering effects usually decrease from the outside to the interior of the meteorite. The results of evolved gas analysis indicate that variation in weathering between surface and core is not significant in respect to the formation of Fe-oxyhydroxides. The secondary alteration effects in the noble gases are distributed unevenly throughout the specimens, as seen in the nonsystematic differences observed for the heavy noble gases. Chemical analyses show significant enrichment of Ba and Sr in the outer parts of the weathered samples due to element contamination through aqueous solution. Iron, Ni, and Co are partly flushed from the system as the metal oxidation proceeds. Oxygen isotopes show increases in delta(sup 18)O and delta(sup 17)O with increasing terrestrial age. For a set of H3 chondrites, the degree of weathering determined from the water content was correlated with terrestrial ages and is discussed with respect to possible weathering mechanisms.