Composition of matrix in the CR chondrite LAP 02342     

John T. Wasson  Alan E. Rubin 《Geochimica et cosmochimica acta》2009,73(5):1436-325

We report evidence of interchondrule matrix heterogeneity on a scale of ∼50 μm in the well-preserved CR2 chondrite LAP 02342. Despite minor effects resulting from asteroidal aqueous alteration, the matrix in this CR chondrite seems to preserve much of the compositional record of nebular fines. We carried out electron-microprobe studies using a 3-μm-diameter beam; we analyzed 10 elements in 36- or 49-point grids on 11 ca. 50 × 50-μm rectangular areas of matrix. Each grid area has a distinct composition, inconsistent with a simple model of matrix material having a uniform composition throughout the nebular formation region of the CR chondrites. On S-Fe, Mg-Si, K-Na and K-Al scatter diagrams, the grid areas (i.e., different matrix patches) are largely separated from each other; plots of means with 95% confidence limits demonstrate that the compositions are resolvable. Five matrix areas were analyzed again in duplicate runs; excellent agreement was observed between duplicate studies. LAP 02342 experienced two forms of mild aqueous alteration - as patchy enrichments in Ca (inferred to reflect CaCO₃) and as regions in which sulfide laths are embedded within phyllosilicates. Despite this evidence of aqueous transport, the effect on the composition of matrix is not resolvable. For example, matrix points that were adjacent to points with high CaCO₃ contents show elemental concentrations similar to those in regions having only one or two points with a Ca enrichment. It appears that secondary minerals are found in areas where there are suitable precursor phases and voids into which new phases could grow unimpeded. Calcium appears to be unique in forming a phase that greatly lowers the Ca⁺⁺ content of the aqueous medium, thus enhancing the rate of diffusion. Because chondrules vary widely in bulk composition, the formation of chondrules in small sets (100 or less) could generate “smoke” and mesostasis spray with compositions unique to each set. However, if these nanoparticles were moving independently in the nebula, it would not have been possible to have preserved compositional variations. We therefore infer that the anomalous materials were preserved in small nebular structures, probably as porous chondrules formed by low degrees of melting.  相似文献   

Mn-Cr systematics of carbonates in CM chondrites: Implications for the timing and duration of aqueous alteration     

Simone de Leuw  Alan E. Rubin  John T. Wasson 《Geochimica et cosmochimica acta》2009,73(24):7433-2751

CM chondrites contain carbonates and other secondary minerals such as phyllosilicates, sulfides, sulfates, oxides and hydroxides that are believed to have formed by aqueous alteration reactions on their parent asteroid. We report in situ Mn-Cr isotope measurements in the highly aqueously altered CM2.1 chondrites QUE 93005 and ALH 83100 using secondary ion mass spectrometry (Cameca ims-1270 ion microprobe). The ⁵³Cr excesses are correlated with the ⁵³Mn/⁵⁵Mn ratio and result from the in situ decay of ⁵³Mn, a short-lived radioisotope with a half-life of 3.7 Ma. If we assume that carbonate grains in samples QUE 93005 and ALH 83100 are cogenetic, then the excesses define initial ⁵³Mn/⁵⁵Mn ratios ((⁵³Mn/⁵⁵Mn)₀) of (4.1 ± 1.2) × 10⁻⁶ and (5.1 ± 1.7) × 10⁻⁶, respectively. These values are comparable to those in carbonates from other CM chondrites as reported in the literature. Initial ⁵³Mn/⁵⁵Mn ratios for calculated model isochrones for individual carbonate grains range from (3.8 ± 1.4) × 10⁻⁶ to (4.8 ± 2.1) × 10⁻⁶ for QUE 93005 and from (3.1 ± 1.6) × 10⁻⁶ to (1.3 ± 0.5) × 10⁻⁵ for ALH 83100. A possible interpretation for the ranges in (⁵³Mn/⁵⁵Mn)₀ could be that alteration in individual CM chondrites was episodic and occurred over an extended period of time. However, isochrones based on the entire set of carbonate grains in each of the CM chondrites imply that the degree of aqueous alteration is roughly correlated with the age of carbonate formation in CM chondrites of different subtypes and that alteration on the CM parent asteroid started contemporaneously with or shortly after CAI formation and lasted at least 4 Ma.  相似文献   

Compositions of three low-FeO ordinary chondrites: Indications of a common origin with the H chondrites     

Julianne Troiano  Mark L. Rivers 《Geochimica et cosmochimica acta》2011,75(21):6511-6519

Burnwell, EET 96031, and LAP 04575 are ordinary chondrites (OC) that possess lower than typical olivine Fa content than has been established for the H chondrites (<∼17 mol%). Mean low-Ca pyroxene Fs contents are typically lower than mean Fa content, with generally ?16 mol% Fs. We have investigated these three low-FeO chondrites by measuring their trace element abundances, oxygen isotopic compositions, and examining their three-dimensional (3D) petrography with synchrotron X-ray microtomography. We compare our results with those established for more common OC. The low FeO chondrites studied here have bulk trace element abundances that are identical to the H chondrites. From bulk oxygen isotopic analysis, we show that Burnwell, EET 96010, and LAP 04757 sampled oxygen reservoirs identical to the H chondrites. Burnwell, EET 96031, and LAP 04575 possess common 3D opaque mineral structures that could be distinct from the H chondrites, as evidenced by X-ray microtomographic analysis, but our comparison suite of H chondrites is small and unrepresentative. Overall, our data suggest a common origin for the low-FeO chondrites Burnwell, EET 96010, and LAP 04757 and the H chondrites. These three samples are simply extreme members of a redox process where a limiting nebular oxidizing agent, probably ice, reacted with material containing slightly higher amounts of metal than typically seen in the H chondrites.  相似文献   

A comparative study of the hydroxy acids from the Murchison, GRA 95229 and LAP 02342 meteorites     

Sandra Pizzarello  Yi Wang 《Geochimica et cosmochimica acta》2010,74(21):6206-7595

The hydroxy acid suites extracted from the Murchison (MN), GRA 95229 (GRA) and LAP 02342 (LAP) meteorites have been investigated for their molecular, chiral and isotopic composition. Substantial amounts of the compounds have been detected in all three meteorites, with a total abundance that is lower than that of the amino acids in the same stones. Overall, their molecular distributions mirror closely that of the corresponding amino acids and most evidently so for the LAP meteorite. A surprising l-lactic acid enantiomeric excess was found present in all three stones, which cannot be easily accounted by terrestrial contamination; all other compounds of the three hydroxy acid suites were found racemic. The branched-chain five carbon and the diastereomer six-carbon hydroxy acids were also studied vis-a-vis the corresponding amino acids and calculated ab initio thermodynamic data, with the comparison allowing the suggestion that meteoritic hydroxyacid at these chain lengths formed under thermodynamic control and, possibly, at a later stage than the corresponding amino acids. ¹³C and D isotopic enrichments were detected for many of the meteoritic hydroxy acids and found to vary between molecular species with trends that also appear to correlate to those of amino acids; the highest δD value (+3450‰) was displayed by GRA 2-OH-2-methylbutyric acid. The data suggest that, while the amino- and hydroxy acids likely relate to common presolar precursor, their final distribution in meteorites was determined to large extent by the overall composition of the environments that saw their formation, with ammonia being the determining factor in their final abundance ratios.  相似文献   

Nature of volatile depletion and genetic relationships in enstatite chondrites and aubrites inferred from Zn isotopes   总被引：1，自引：0，他引：1  

Frédéric Moynier  Randal C. Paniello  Francis Albarède  Frank Podosek 《Geochimica et cosmochimica acta》2011,75(1):297-271

Enstatite meteorites include the undifferentiated enstatite chondrites and the differentiated enstatite achondrites (aubrites). They are the most reduced group of all meteorites. The oxygen isotope compositions of both enstatite chondrites and aubrites plot along the terrestrial mass fractionation line, which suggests some genetic links between these meteorites and the Earth as well.For this study, we measured the Zn isotopic composition of 25 samples from the following groups: aubrites (main group and Shallowater), EL chondrites, EH chondrites and Happy Canyon (impact-melt breccia). We also analyzed the Zn isotopic composition and elemental abundance in separated phases (metal, silicates, and sulfides) of the EH4, EL3, and EL6 chondrites. The different groups of meteorites are isotopically distinct and give the following values (‰): aubrite main group (−7.08 < δ⁶⁶Zn < −0.37); EH3 chondrites (0.15 < δ⁶⁶Zn < 0.31); EH4 chondrites (0.15 < δ⁶⁶Zn < 0.27); EH5 chondrites (δ⁶⁶Zn = 0.27 ± 0.09; n = 1); EL3 chondrites (0.01 < δ⁶⁶Zn < 0.63); the Shallowater aubrite (1.48 < δ⁶⁶Zn < 2.36); EL6 chondrites (2.26 < δ⁶⁶Zn < 7.35); and the impact-melt enstatite chondrite Happy Canyon (δ⁶⁶Zn = 0.37).The aubrite Peña Blanca Spring (δ⁶⁶Zn = −7.04‰) and the EL6 North West Forrest (δ⁶⁶Zn = 7.35‰) are the isotopically lightest and heaviest samples, respectively, known so far in the Solar System. In comparison, the range of Zn isotopic composition of chondrites and terrestrial samples (−1.5 < δ⁶⁶Zn < 1‰) is much smaller ( [Luck et al., 2005] and [Herzog et al., 2009]).EH and EL3 chondrites have the same Zn isotopic composition as the Earth, which is another example of the isotopic similarity between Earth and enstatite chondrites. The Zn isotopic composition and abundance strongly support that the origin of the volatile element depletion between EL3 and EL6 chondrites is due to volatilization, probably during thermal metamorphism. Aubrites show strong elemental depletion in Zn compared to both EH and EL chondrites and they are enriched in light isotopes (δ⁶⁶Zn down to −7.04‰). This is the opposite of what would be expected if Zn elemental depletion was due to evaporation, assuming the aubrites started with an enstatite chondrite-like Zn isotopic composition. Evaporation is therefore not responsible for volatile loss from aubrites. On Earth, Zn isotopes fractionate very little during igneous processes, while differentiated meteorites show only minimal Zn isotopic variability. It is therefore very unlikely that igneous processes can account for the large isotopic fractionation of Zn in aubrites. Condensation of an isotopically light vapor best explains Zn depletion and isotopically light Zn in these puzzling rocks. Mass balance suggests that this isotopically light vapor carries Zn lost by the EL6 parent body during thermal metamorphism and that aubrites evolved from an EL6-like parent body. Finally, Zn isotopes suggest that Shallowater and aubrites originate from distinct parent bodies.  相似文献   

Opaque phases in type-II chondrules from CR2 chondrites: Implications for CR parent body formation     

Devin L. Schrader  Harold C. Connolly Jr.  Dante S. Lauretta 《Geochimica et cosmochimica acta》2008,72(24):6124-6140

We report the results of a detailed study of sulfide-bearing opaque assemblages from the MAC 87320, EET 92011, and Renazzo CR carbonaceous chondrites. The objectives of this study are to (1) characterize sulfide and associated phases within CR2 chondrites; (2) determine the petrographic relationship between sulfides, metals, and chondrules; (3) constrain the history of type-II chondrules; (4) ascertain the environments in which type-II chondrules formed and were altered; and (5) unravel the formation and alteration history of the CR parent body as recorded in sulfide-bearing assemblages. Sulfide-bearing opaque assemblages occur primarily within type-II (FeO-rich) chondrules. The sulfide assemblages are concentrated near the chondrule edges. Assemblages in MAC 87320 are composed of troilite, phosphate, and Ni-rich metal. EET 92011 contains assemblages composed of pentlandite, troilite, and Ni-rich metal. The assemblages in Renazzo contain tochilinite, magnetite, troilite, pentlandite, and phosphate. In all of the assemblages in Renazzo the tochilinite is fine grained and intimately mixed with troilite, pentlandite, or magnetite. Opaque assemblages in CR chondrites record a complex history that includes both high- and low-temperature processes. The morphology and composition of sulfides in CR2 chondrites suggests that the sulfide-bearing assemblages originally formed in gas-solid reactions in the nebula at temperatures above the Fe-FeS eutectic (988 °C). Many of the assemblages were subsequently aqueously altered on the CR-chondrite parent body to various degrees at temperatures from ∼50 to 200 °C. We combine these observations and interpretations to provide a detailed model of the history of the CR parent body.  相似文献   

Compositions of four unusual CM or CM-related Antarctic chondrites     

Gina M. Moriarty  Douglas Rumble III 《Chemie der Erde / Geochemistry》2009,69(2):161-2323

To identify chemical group affinities and infer the occurrence of thermal metamorphism or aqueous alteration in their histories, we quantified 43 trace elements in the CM or CM-related Antarctic carbonaceous chondrites EET 96010, LAP 02277, MET 01070, and WIS 91600. We also analyzed LAP 02206, a CV chondrite, to add to our comparison database. We present whole-rock oxygen isotope data for LAP 02206, LAP 02277, and MET 01070 to complement our trace element results. With these data, we confirm the CV classification of LAP 02206 and CM or CM-like classification for the other four chondrites in this study. On the basis of moderately volatile element content, our results show that EET 96010 experienced open-system heating, while any heating LAP 02277 and MET 01070 may have experienced was in a chemically closed-system. WIS 91600, on a trace element basis, appears to be CM-like material. Our analyses support the idea that CM material has experienced a wide variety of post-accretionary processing.  相似文献   

Deuterium enrichments in chondritic macromolecular material—Implications for the origin and evolution of organics, water and asteroids     

C.M.O’D. Alexander  S.D. Newsome  L.R. Nittler  G.D. Cody 《Geochimica et cosmochimica acta》2010,74(15):4417-7532

Here we report the elemental and isotopic compositions of the insoluble organic material (IOM) isolated from several previously unanalyzed meteorites, as well as the reanalyses of H isotopic compositions of some previously measured samples (Alexander et al., 2007). The IOM in ordinary chondrites (OCs) has very large D enrichments that increase with increasing metamorphism and decreasing H/C, the most extreme δD value measured being almost 12,000‰. We propose that such large isotopic fractionations could be produced in the OC parent bodies through the loss of isotopically very light H₂ generated when Fe was oxidized by water at low temperatures (<200 °C). We suggest that similar isotopic fractionations were not generated in the IOM of CV and CO chondrites with similar metamorphic grades and IOM H/C ratios because proportionately less water was consumed during metamorphism, and the remaining water buffered the H isotopic composition of the IOM even a H was being lost from it.Hydrogen would also have been generated during the alteration of CI, CM and CR carbonaceous chondrites. The IOM in these meteorites exhibit a considerable range in isotopic compositions, but all are enriched in D, as well as ¹⁵N, relative to terrestrial values. We explore whether these enrichments could also have been produced by the loss of H₂, but conclude that the most isotopically anomalous IOM compositions in meteorites from these groups are probably closest to their primordial values. The less isotopically anomalous IOM has probably been modified by parent body processes. The response of IOM to these processes was complex and varied, presumably reflecting differences in conditions within and between parent bodies.The D enrichments associated with H₂ generation, along with exchange between D-rich IOM and water in the parent bodies, means that it is unlikely that any chondrites retain the primordial H isotopic composition of the water ice that they accreted. The H isotopic compositions of the most water-rich chondrites, the CMs and CIs, are probably the least modified and their compositions (δD ? −25‰) suggest that their water did not form at large radial distances from the Sun where ice is predicted to be very D-rich. Yet models to explain the O isotopic composition of inner Solar System bodies require that large amounts of ice were transported from the outer to the inner Solar System.  相似文献   

Graves Nunataks 95209: A snapshot of metal segregation and core formation     

T.J. McCoy  W.D. Carlson  R.M. Stroud  D.H. Garrison 《Geochimica et cosmochimica acta》2006,70(2):516-531

GRA 95209 may provide our best opportunity to date to understand the earliest stages of core formation in asteroidal bodies. This lodranite preserves a physically, chemically, and mineralogically complex set of metal-sulfide veins. High-resolution X-ray computed tomography revealed three distinct lithologies. The dominant mixed metal-silicate-sulfide matrix is cut by metal-rich, graphite-bearing veins exceeding 1 cm in width and grades into a volumetrically minor metal-poor region. Silicate compositions and modal abundances are typical for lodranites, while the mineralogy of the metal-sulfide component is complex and differs among the three lithologies. Kamacite and troilite occur with chromite, tetrataenite, schreibersite, graphite, and a range of phosphates. An ³⁹Ar-⁴⁰Ar age of 4.521 ± 0.006 Ga measures the time of closure of the K-Ar system. Carbon rosettes within the metal-rich vein are nitrogen-poor, well crystallized, include kamacite sub-grains of composition comparable to the host metal, and are essentially isotopically homogeneous (δ¹³C ∼ −33‰). In contrast, carbon rosettes within metal of the metal-poor lithology are N-poor, poorly crystallized, include kamacite grains that are Ni-poor compared to their host metal, and are isotopically heterogeneous (δ¹³C ranging from −50 to +80‰) even within a single metal grain. The silicate portion of GRA 95209 is similar to the lodranite EET 84302, sharing a common texture, silicate mineral compositions, and Ar-Ar age. GRA 95209 and EET 84302 are intermediate between acapulcoites and lodranites. Both experienced Fe,Ni-FeS melting with extensive melt migration, but record only the onset of silicate partial melting with limited migration of silicate melt. The complex metal-sulfide veins in GRA 95209 resulted from low-degree partial melting and melt migration and intruded the matrix lithology. Reactions between solid minerals and melt, including oxidation-reduction reactions, produced the array of phosphates, schreibersite, and tetrataenite. Extensive reduction in the metal-rich vein resulted from its origin in a hotter portion of the asteroid. This difference in thermal history is supported by the graphite structures and isotopic compositions. The graphite rosettes in the metal-rich vein are consistent with high-temperature igneous processing. In contrast, the carbon in the metal-poor lithology appears to preserve a record of formation in the nebula prior to parent-body formation. Carbon incorporated from the solar nebula into a differentiating asteroid is preferentially incorporated in metal-sulfide melts that form a core, but does not achieve isotopic homogeneity until extensive thermal processing occurs.  相似文献   

Oxygen isotopic compositions of chondrules from the metal-rich chondrites Isheyevo (CH/CB_b), MAC 02675 (CB_b) and QUE 94627 (CB_b)     

Alexander N. Krot  Kazuhide Nagashima  Hisayoshi Yurimoto 《Geochimica et cosmochimica acta》2010,74(7):2190-7611

It has been recently suggested that (1) CH chondrites and the CB_b/CH-like chondrite Isheyevo contain two populations of chondrules formed by different processes: (i) magnesian non-porphyritic (cryptocrystalline and barred) chondrules, which are similar to those in the CB chondrites and formed in an impact-generated plume of melt and gas resulted from large-scale asteroidal collision, and (ii) porphyritic chondrules formed by melting of solid precursors in the solar nebula. (2) Porphyritic chondrules in Isheyevo and CH chondrites are different from porphyritic chondrules in other carbonaceous chondrites ( [Krot et al., 2005], [Krot et al., 2008a] and [Krot et al., 2008b]). In order to test these hypotheses, we measured in situ oxygen isotopic compositions of porphyritic (magnesian, Type I and ferroan, Type II) and non-porphyritic (magnesian and ferroan cryptocrystalline) chondrules from Isheyevo and CB_b chondrites MAC 02675 and QUE 94627, paired with QUE 94611, using a Cameca ims-1280 ion microprobe.On a three-isotope oxygen diagram (δ¹⁷O vs. δ¹⁸O), compositions of chondrules measured follow approximately slope-1 line. Data for 19 magnesian cryptocrystalline chondrules from Isheyevo, 24 magnesian cryptocrystalline chondrules and 6 magnesian cryptocrystalline silicate inclusions inside chemically-zoned Fe,Ni-metal condensates from CB_b chondrites have nearly identical compositions: Δ¹⁷O = −2.2 ± 0.9‰, −2.3 ± 0.6‰ and −2.2 ± 1.0‰ (2σ), respectively. These observations and isotopically light magnesium compositions of cryptocrystalline magnesian chondrules in CB_b chondrites (Gounelle et al., 2007) are consistent with their single-stage origin, possibly as gas-melt condensates in an impact-generated plume. In contrast, Δ¹⁷O values for 11 Type I and 9 Type II chondrules from Isheyevo range from −5‰ to +4‰ and from −17‰ to +3‰, respectively. In contrast to typical chondrules from carbonaceous chondrites, seven out of 11 Type I chondrules from Isheyevo plot above the terrestrial fractionation line. We conclude that (i) porphyritic chondrules in Isheyevo belong to a unique population of objects, suggesting formation either in a different nebular region or at a different time than chondrules from other carbonaceous chondrites; (ii) Isheyevo, CB and CH chondrites are genetically related meteorites: they contain non-porphyritic chondrules produced during the same highly-energetic event, probably large-scale asteroidal collision; (iii) the differences in mineralogy, petrography, chemical and whole-rock oxygen isotopic compositions between CH and CB chondrites are due to various proportions of the nebular and the impact-produced materials.  相似文献   

Modal mineralogy of CM chondrites by X-ray diffraction (PSD-XRD): Part 2. Degree, nature and settings of aqueous alteration     

K.T. Howard  G.K. Benedix  P.A. Bland  G. Cressey 《Geochimica et cosmochimica acta》2011,75(10):2735-7828

Within 5 million years after formation of calcium aluminium rich inclusions (CAI), high temperature anhydrous phases were transformed to hydrous phyllosilicates, mostly serpentines, which dominate the matrices of the most primitive carbonaceous chondrites. CMs are the largest group of meteorites to provide samples of this material. To understand the nature of the availability, and role of H₂O in the early solar system - as well as the settings of aqueous alteration - defining CM petrogenesis is critical. By Position Sensitive Detector X-ray Diffraction (PSD-XRD), we determine the modal abundance of crystalline phases present in volumes >1% for a suite of CMs - extending Part 1 of this work that dealt only with CM2 falls (Howard et al., 2009) to now include CM2 and CM1 finds. CM2 samples contain 13-31% Fe,Mg silicates (olivine + pyroxene) and from 67% to 82% total phyllosilicate (mean 75% ± 1.3 2σ). CM1 samples contain 6-10% olivine + pyroxene and 86-88% total phyllosilicate. Magnetite (0.6-5.2%), sulphide (0.6-3.9%), calcite (0-1.9%) and gypsum (0-0.8%) are minor phases across all samples. Since phyllosilicate forms from hydration of anhydrous Fe,Mg silicates (olivine + pyroxene), the ratio of total phyllosilicate to total anhydrous Fe,Mg silicate defines the degree of hydration and the following sequence results (in order of increasing hydration): QUE 97990 < Y 791198 < Murchison < Murray < Mighei < ALHA 81002 < Nogoya ? Cold Bokkeveld ? Essebi < QUE 93005 < ALH 83100 < MET 01070 < SCO 06043. High activities of Al (mostly from reactive mesostasis) and Si help to explain the composition and structure of CM serpentines that are distinct from terrestrial standards. Our data allows inference as to CM mineralogy at the point of accretion and challenges the conceptual validity of progressive alteration sequences. Modal mineralogy also provides new insights into CM petrogenesis and hints at a component of aqueous alteration occurring in the nebula, in addition to on the CM parent body(ies).  相似文献   

Non-nebular origin of dark mantles around chondrules and inclusions in CM chondrites     

Josep M. Trigo-Rodriguez  Alan E. Rubin 《Geochimica et cosmochimica acta》2006,70(5):1271-1290

Our examination of nine CM chondrites that span the aqueous alteration sequence leads us to conclude that compact dark fine mantles surrounding chondrules and inclusions in CM chondrites are not discrete fine-grained rims acquired in the solar nebula as modeled by Metzler et al. [Accretionary dust mantles in CM chondrites: evidence for solar nebula processes. Geochim. Cosmochim. Acta56, 1992, 2873-2897]. Nebular processes that lead to agglomeration produce materials with porosities far higher than those in the dark mantles. We infer that the mantles were produced from porous nebular materials on the CM parent asteroid by impact-compaction (a process that produces the lowest porosity adjacent to chondrules and inclusions). Compaction was followed by aqueous alteration that formed tochilinite, serpentine, Ni-bearing sulfide, and other secondary products in voids in the interchondrule regions. Metzler et al. reported a correlation between mantle thickness and the radius of the enclosed object. In Yamato 791198 we find no correlation when all sizes of central objects and dark lumps are included but a significant correlation (r² = 0.44) if we limit consideration to central objects with radii >35 μm; a moderate correlation is also found in QUE 97990. We suggest that impact-induced shear of a plum-pudding-like precursor produced the observed “mantles”; these were shielded from comminution during impact events by the adjacent stronger chondrules and inclusions. Some mantles in CM chondrites with low degrees of alteration show distinct layers that may largely reflect differences in porosity. Typically, a gray, uniform inner layer is surrounded by an outer layer consisting of darker silicates with BSE-bright speckles. The CM-chondrite objects characterized as “primary accretionary rocks” by Metzler et al. did not form in the nebula, but rather on the parent body. The absence of solar-flare particle tracks and solar-wind-implanted rare gases in these clasts reflect their lithified nature and low surface/volume ratios during the period when they resided in the regolith and were subject to irradiation by solar particles. The clasts are analogous to the light-colored metamorphosed clasts in ordinary-chondrite regolith breccias (which also lack solar-flare particle tracks and solar-wind gas).  相似文献   

The LaPaz Icefield 04840 meteorite: Mineralogy, metamorphism, and origin of an amphibole- and biotite-bearing R chondrite     

M.C. McCanta  A.H. Treiman  C.M.O’D. Alexander  E.J. Essene 《Geochimica et cosmochimica acta》2008,72(23):5757-5780

The R chondrite meteorite LaPaz Icefield (LAP) 04840 is unique among metamorphosed, non-carbonaceous chondrites in containing abundant OH-bearing silicate minerals: ∼13% ferri-magnesiohornblende and ∼0.4% phlogopite by volume. Other minerals include olivine (Fo₆₂), orthopyroxene (En₆₉Fs₃₀Wo₁), albite (An₈Ab₉₀Or₂), magnetite, pyrrhotite, pentlandite, and apatite. Ferromagnesian minerals are rich in Fe³⁺, as determined by Mössbauer spectrometry and electron microprobe chemical analyses. Fe³⁺/Fe_tot values are olivine ?5%, amphibole 80%, phlogopite 65%, and magnetite 42%. Mineral compositions are nearly constant across grains and the section, except for a small variability in amphibole compositions reflecting the edenite exchange couple (^ANa + ^IVAl ↔ ^A□ + Si). These mineral compositions, the absence of Fe-Ni metal, and the oxygen isotope data support its classification as an R (Rumuruti) chondrite. LAP 04840 is classified as petrologic grade 5, based on the chemical homogeneity of its minerals, and the presence of distinctly marked chondrules and chondrule fragments in a fine-grained crystalline matrix. The mineral assemblage of LAP 04840 allows calculation of physical and chemical conditions at the peak of its metamorphism: T = 670 ± 60 °C from a amphibole-plagioclase thermometer; P_H2O between 250 and 500 bars as constrained by the assemblage phlogopite + orthopyroxene + olivine + feldspar and the absence of diopside; P_CO2 unconstrained; f_O2 at QFM + 0.5 log units; . The hydrogen in LAP 04840 is very heavy, an average δD value of +3660 ± 75‰ in the magnesiohornblende. Only a few known sources of hydrogen have such high δD and are suitable sources for LAP 04840: ordinary chondrite phyllosilicates (as in the Semarkona chondrite), and insoluble organic matter (IOM) in ordinary chondrites and CR chondrites. Hydrogen from the IOM could have been released by oxidation, and then reacted with an anhydrous R chondrite (at high temperature), but it is not clear whether this scenario is correct.  相似文献   

Temperatures of aqueous alteration and evidence for methane generation on the parent bodies of the CM chondrites     

Weifu Guo  John M. Eiler 《Geochimica et cosmochimica acta》2007,71(22):5565-5575

Aqueous alteration of primitive meteorites was among the earliest geological processes during the evolution of our solar system. ‘Clumped-isotope’ thermometry of carbonates in the CM chondrites, Cold Bokkeveld, Murray, and Murchison, demonstrates that they underwent aqueous alteration at 20-71 °C from a fluid with δ¹⁸O_VSMOW of 2.0‰ to 8.1‰ and δ¹⁷O_VSMOW of −0.1‰ to 3.0‰. The δ¹³C_VPDB values of these carbonates exhibit a negative correlation with the δ¹⁸O_VSMOW of their formation waters, consistent with formation and escape of ¹³C-depleted CH₄ during aqueous alteration. Methane generation under these conditions implies that the alteration fluid was characterized by an Eh ? −0.67 and pH ? 12.5 (or lower at the highest alteration temperatures). Our findings suggest that methane generation may have been a widespread consequence of planetesimal and planetary aqueous alteration, perhaps explaining the occurrence of methane on Titan, Triton, Pluto, and other Kuiper-belt objects.  相似文献   

Oxygen- and magnesium-isotope compositions of calcium-aluminum-rich inclusions from CR2 carbonaceous chondrites     

Kentaro Makide  Alexander N. Krot  Gary R. Huss  Addi Bischoff 《Geochimica et cosmochimica acta》2009,73(17):5018-325

We report both oxygen- and magnesium-isotope compositions measured in situ using a Cameca ims-1280 ion microprobe in 20 of 166 CAIs identified in 47 polished sections of 15 CR2 (Renazzo-type) carbonaceous chondrites. Two additional CAIs were measured for oxygen isotopes only. Most CR2 CAIs are mineralogically pristine; only few contain secondary phyllosilicates, sodalite, and carbonates - most likely products of aqueous alteration on the CR2 chondrite parent asteroid. Spinel, hibonite, grossite, anorthite, and melilite in 18 CAIs have ¹⁶O-rich (Δ¹⁷O = −23.3 ± 1.9‰, 2σ error) compositions and show no evidence for postcrystallization isotopic exchange commonly observed in CAIs from metamorphosed CV carbonaceous chondrites. The inferred initial ²⁶Al/²⁷Al ratios, (²⁶Al/²⁷Al)₀, in 15 of 16 ¹⁶O-rich CAIs measured are consistent with the canonical value of (4.5-5) × 10⁻⁵ and a short duration (<0.5 My) of CAI formation. These data do not support the “supra-canonical” values of (²⁶Al/²⁷Al)₀ [(5.85-7) × 10⁻⁵] inferred from whole-rock and mineral isochrons of the CV CAIs. A hibonite-grossite-rich CAI El Djouf 001 MK #5 has uniformly ¹⁶O-rich (Δ¹⁷O = −23.0 ± 1.7‰) composition, but shows a deficit of ²⁶Mg and no evidence for ²⁶Al. Because this inclusion is ¹⁶O-rich, like CAIs with the canonical (²⁶Al/²⁷Al)₀, we infer that it probably formed early, like typical CAIs, but from precursors with slightly nonsolar magnesium and lower-than-canonical ²⁶Al abundance. Another ¹⁶O-enriched (Δ¹⁷O = −20.3 ± 1.2‰) inclusion, a spinel-melilite CAI fragment Gao-Guenie (b) #3, has highly-fractionated oxygen- and magnesium-isotope compositions (∼11 and 23‰/amu, respectively), a deficit of ²⁶Mg, and a relatively low (²⁶Al/²⁷Al)₀ = (2.0 ± 1.7) × 10⁻⁵. This could be the first FUN (Fractionation and Unidentified Nuclear effects) CAI found in CR2 chondrites. Because this inclusion is slightly ¹⁶O-depleted compared to most CR2 CAIs and has lower than the canonical (²⁶Al/²⁷Al)₀, it may have experienced multistage formation from precursors with nonsolar magnesium-isotope composition and recorded evolution of oxygen-isotope composition in the early solar nebula over  My. Eight of the 166 CR2 CAIs identified are associated with chondrule materials, indicating that they experienced late-stage, incomplete melting during chondrule formation. Three of these CAIs show large variations in oxygen-isotope compositions (Δ¹⁷O ranges from −23.5‰ to −1.7‰), suggesting dilution by ¹⁶O-depleted chondrule material and possibly exchange with an ¹⁶O-poor (Δ¹⁷O > −5‰) nebular gas. The low inferred (²⁶Al/²⁷Al)₀ ratios of these CAIs (<0.7 × 10⁻⁵) indicate melting >2 My after crystallization of CAIs with the canonical (²⁶Al/²⁷Al)₀ and suggest evolution of the oxygen-isotope composition of the inner solar nebula on a similar or a shorter timescale. Because CAIs in CR2 and CV chondrites appear to have originated in a similarly ¹⁶O-rich reservoir and only a small number of CR2 and CV CAIs were affected by chondrule melting events in an ¹⁶O-poor gaseous reservoir, the commonly observed oxygen-isotope heterogeneity in CAIs from metamorphosed CV chondrites is most likely due to fluid-solid isotope exchange on the CV asteroidal body rather than gas-melt exchange. This conclusion does not preclude that some CV CAIs experienced oxygen-isotope exchange during remelting, instead it implies that such remelting is unlikely to be the dominant process responsible for oxygen-isotope heterogeneity in CV CAIs. The mineralogy, oxygen and magnesium-isotope compositions of CAIs in CR2 chondrites are different from those in the metal-rich, CH and CB carbonaceous chondrites, providing no justification for grouping CR, CH and CB chondrites into the CR clan.  相似文献