Carbonaceous chondrites of the Ornans type: A metamorphic sequence     

Harry Y. McSween 《Geochimica et cosmochimica acta》1977,41(4):477-491

C3(O) chondrites comprise a metamorphic sequence. The following order reflects increasing grade: Kainsaz. Felix. Ornans. Lance. Isna, Warrenton. Assignment of Karoonda to the Ornans subtype is uncertain, but it is certainly of higher petrologic type than C3. Average olivine and pyroxene compositions in the metamorphic sequence change progressively from Fo₁₂. Fs₃ to Fo₃₄, Fs₁₁, respectively, and per cent mean deviation decreases. Kamacite and taenite change composition with increasing grade, reflecting higher equilibration temperatures. Blurring of textural features and Fe/Mg exchange between matrix and inclusions are also evident. As in the ordinary chondrites. contents of rare gases and possibly volatiles correlate with degree of metamorphism, but the effects are small. The meteorite Ornans presents an intriguing paradox. Observed chemical enrichment and depletion patterns reflect a higher metamorphic grade than do petrographic properties. The data suggest that abundance patterns of volatile components were not generated by metamorphism, but may represent primary differences. Strong correlations present in other C3(O) chondrites indicate some genetic link between metamorphism and composition, although the relationship is probably not causal. The autometamorphism model of Larimer and Anders (1967) appears to be the most straightforward explanation, but an observed negative correlation between the amount of matrix and content of volatiles suggests a re-examination of the two-component model. The decoupling mechanism required for Ornans is uncertain.  相似文献   

Dark inclusions in CO3 chondrites: new indicators of parent-body processes     

Daisuke Itoh 《Geochimica et cosmochimica acta》2003,67(1):153-169

A petrographic and scanning electron microscopic study of the four CO3 chondrites Kainsaz, Ornans, Lancé, and Warrenton reveals for the first time that dark inclusions (DIs) occur in all the meteorites. DIs are mostly smaller in size than those reported from CV3 chondrites. They show evidence suggesting that they were formed by aqueous alteration and subsequent dehydration of a chondritic precursor and so probably have a formation history similar to that of DIs in CV3 chondrites. DIs in the CO3 chondrites consist mostly of fine-grained, Fe-rich olivine and can be divided into two types on the basis of texture. Type I DIs contain rounded, porous aggregates of fine grains in a fine-grained matrix and have textures suggesting that they are fragments of chondrule pseudomorphs. Veins filled with Fe-rich olivine are common in type I DIs, providing evidence that they experienced aqueous alteration on the parent body. Type II DIs lack rounded porous aggregates and have a matrix-like, featureless texture. Bulk chemical compositions of DIs and mineralogical characteristics of olivine grains in DIs suggest that these two types of DIs have a close genetic relationship.The DIs are probably clasts that have undergone aqueous alteration and subsequent dehydration at a location different from the present location in the meteorites. The major element compositions, the mineralogy of metallic phases, and the widely dispersed nature of the DIs suggest that their precursor was CO chondrite material. The CO parent body has been commonly regarded to have been dry, homogeneous, and unprocessed. However, the DIs suggest that the CO parent body was a heterogeneous conglomerate consisting of water-bearing regions and water-free regions and that during asteroidal heating, the water-bearing regions were aqueously altered and subsequently dehydrated. Brecciation may also have been active in the parent body.The DIs and the matrices are similarly affected by thermal metamorphism in their own host CO3 chondrites (petrologic subtypes 3.1 to 3.6), but the degree of the secondary processing (aqueous alteration and subsequent dehydration) of the DIs has no apparent correlation with the petrologic grades of the host chondrites. These observations suggest that the DIs had been incorporated into the host chondrites before the thermal metamorphism took place and that the secondary processes that affected the DIs largely occurred before the thermal metamorphism.  相似文献   

Pb-Pb dating constraints on the accretion and cooling history of chondrites     

Audrey Bouvier  Janne Blichert-Toft  Jeffrey D. Vervoort 《Geochimica et cosmochimica acta》2007,71(6):1583-1604

We have analyzed the Pb isotopic compositions of whole-rocks and various components (CAIs, chondrules, and/or mineral separates) of two carbonaceous chondrites, Allende (CV3) and Murchison (CM2), and nine ordinary chondrites, Sainte Marguerite (H4), Nadiabondi and Forest City (H5), Kernouvé (H6), Bjurböle (L/LL4), Elenovka and Ausson (L5), Tuxtuac (LL5), and Saint-Séverin (LL6) by MC-ICP-MS. Three CAI fractions from Allende define an isochron with an age of 4568.1 ± 9.4 Ma (MSWD = 0.08) and plot on the same isochron as fragments of the Efremovka inclusion E60 analyzed by Amelin et al. [Amelin, Y., Krot, A. N., Hutcheon, I. D., and Ulyanov, A. A. (2002a). Lead isotopic ages of chondrules and calcium-aluminum-rich inclusions. Science297, 1679-1683]. When these two groups of samples are combined, the isochron yields an age of 4568.5 ± 0.5 (MSWD = 0.90), which is our best estimate of the age of the Solar System. Chondrules and pyroxene-olivine fractions from the ordinary chondrites yield ages that reflect the blocking of Pb isotope equilibration with the nebular gas. The combination of these ages with the corresponding metamorphic phosphate ages provides constraints on the thermal history of the different chondrite parent bodies. Among the H chondrites, Sainte Marguerite cooled to below ∼1100 K within a few My at 4565 Ma and to ∼800 K at 4563 Ma. Nadiabondi appears to have experienced a slightly more protracted cooling history with the corresponding interval lasting from 4559 to 4556 Ma. The data from Forest City and Kernouvé show evidence of late-stage perturbation with resulting U/Pb fractionation. Likewise, Pb isotopes in Tuxtuac (LL5) record a cooling history lasting from ∼4555 to 4544 Ma, which may indicate that the cooling history for the LL parent body was more prolonged than for the H parent body. We suggest a thermal evolution model for the growth of the planetary bodies based on the release of radiogenic heat from ²⁶Al and ⁶⁰Fe. This model incorporates the accretion rate, which determines the time at which the radiogenic heat becomes efficiently trapped, and the terminal size of the parent body, which controls its overall thermal inertia. The parent bodies of carbonaceous chondrites, which show little indication of metamorphic transformation, collect cooler nebular material at a relatively late stage. Small asteroids of ∼10-50 km radius accreting within 1-3 My could be the parent bodies of H and LL chondrites. The parent body of the L chondrites is likely to be a larger asteroid (r > 100 km) or possibly the product of collisions of smaller planetary bodies.  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   

Unequilibrated ordinary chondrites: A tentative subclassification based on volatile-element content     

Edward Anders  M.G. Zadnik 《Geochimica et cosmochimica acta》1985,49(5):1281-1291

For unequilibrated ordinary chondrites (= UOC), two measures of primitiveness are available: volatile content, in principle reflecting accretion conditions from the solar nebula, and metamorphism, reflecting reheating in the parent bodies. These two measures do not always correlate, and we have therefore developed a tentative classification scheme based on volatile content that complements the Searset al. (1980) scheme based on metamorphism. Like the latter, it subdivides type 3 chondrites on a scale of 3.0 to 3.9; the notation 3.4/0 indicates a meteorite that is subtype 3.4 according to metamorphism and 3.0 according to volatile content.The classification is based mainly on C and Xe—two elements that are little affected by shock-induced reheating—and to a lesser extent on Ar³⁶,Bi,In, and Tl. Of 22 meteorites considered, the majority have concordant classifications (±0.2) on the two scales. However, 5 meteorites are richer in volatiles than their metamorphic grade indicates: Sharps 3.4/0, ALHA 77011 3.5/0, Ngawi 3.6/3, ALHA 77299 3.7/4, and Mezö-Madaras 3.7/3. It remains to be seen whether these differences indeed denote a more primitive nature.Some new clues to the formation of chondrites may eventually come from Xe and C. Their concentrations in UOC's vary by more than 5×, but the $\text{Xe}\text{C}$ ratio remains nearly constant at 3.4 × 10^?3 of the solar-system ratio. Even the ratios for other chondrite classes differ only slightly from that for UOC's, e.g., C3O (1.5×) and E3,4 (0.4×). Either the 4 factors determining this ratio (T, t, P, and internal surface area of the carbon) varied in complementary fashion, or—more probably—they varied only slightly in the entire source region of chondrites.  相似文献   

The Pb-Pb age of Angrite SAH99555 revisited     

J.N. Connelly  M. Bizzarro  J.A. Baker 《Geochimica et cosmochimica acta》2008,72(19):4813-4824

Representing a suite of well-preserved basaltic meteorites with reported ages from 4566.18 ± 0.14 Ma to 4557.65 ± 0.13 Ma, angrites have been recurring targets for cross-calibrating extinct and absolute chronometers. However, inconsistencies exist in the available chronological data set, including a 4566.18 ± 0.14 Ma Pb-Pb age reported by Baker et al. [Baker J., Bizzarro M., Wittig N., Connelly J. and Haack H. (2005) Early planetesimal melting from an age of 4.5662 Gyr for differentiated meteorites. Nature436, 1127-1131] for Sahara 99555 (herein SAH99555) that is significantly older than a Pb-Pb age for D’Orbigny, despite the two meteorites yielding indistinguishable Hf-W and Mn-Cr ages. We re-evaluate the Pb-Pb age of SAH99555 using a stepwise dissolution procedure on a whole rock fragment and a pyroxene separate. The combined data set yields a linear array that reflects a mixture of radiogenic Pb and terrestrial contamination and corresponds to an age of 4564.58 ± 0.14 Ma, which is 1.60 ± 0.20 Ma younger than that reported by Baker et al. [Baker J., Bizzarro M., Wittig N., Connelly J. and Haack H. (2005) Early planetesimal melting from an age of 4.5662 Gyr for differentiated meteorites. Nature436, 1127-1131]. Our conclusion that SAH99555 crystallized at 4564.58 ± 0.14 Ma requires that all initial Pb was removed in the first progressive dissolution steps, an assertion supported by linearity of data generated by stepwise dissolution of a single fragment and the removal of an obvious highly-radiogenic component early in the dissolution process. We infer that the linear array defined by Baker et al. [Baker J., Bizzarro M., Wittig N., Connelly J. and Haack H. (2005) Early planetesimal melting from an age of 4.5662 Gyr for differentiated meteorites. Nature436, 1127-1131] and their older age reflects a ternary mixture of Pb with constant relative proportions of highly-radiogenic initial Pb and radiogenic Pb with varying amounts of a terrestrial contamination. This requires that the phase harboring the initial Pb is insoluble in 2 M HCl, the only acid applied to the samples by Baker et al. [Baker J., Bizzarro M., Wittig N., Connelly J. and Haack H. (2005) Early planetesimal melting from an age of 4.5662 Gyr for differentiated meteorites. Nature436, 1127-1131] prior to dissolution.  相似文献   

Assessment of the Re decay constant by cross calibration of Re-Os molybdenite and U-Pb zircon chronometers in magmatic ore systems     

David Selby  Robert A. Creaser  Richard J. Markey 《Geochimica et cosmochimica acta》2007,71(8):1999-2013

The past decade has seen renewed interest in ¹⁸⁷Re-¹⁸⁷Os geochronology using a variety of matrices including sulfide minerals, shales and meteorites. The most widely used value of the ¹⁸⁷Re decay constant (λ¹⁸⁷Re) is 1.666 ± 0.005 × 10⁻¹¹ a⁻¹ (±0.31%), which is based on cross calibration of Re-Os and Pb-Pb chronometers for certain meteorites [Smoliar M. I., Walker R. J., and Morgan J. W. (1996) Re-Os isotope constraints on the age of Group IIA, IIIA, IVA, and IVB iron meteorites. Science271, 1099-1102]. However, other recent studies have yielded alternate values of λ¹⁸⁷Re, based upon either direct counting experiments or analysis of meteorites. Here, we provide an independent assessment of λ¹⁸⁷Re, using methodology, sample materials, and preparation of Os standard solutions different from those of Smoliar et al. (1996). Combining Re-Os age data for molybdenite formed in magmatic ore deposits, with the U-Pb zircon age of the magmatic rocks, a refined λ¹⁸⁷Re value is determined by averaging 11 individual cross-calibration experiments spanning ca. 2700 Ma of Earth history. Using the U decay constants of Jaffey [Jaffey A. H., Flynn K. F., Glendenin L. E., Bentley W. C., and Essling A. M. (1971) Precision measurement of half-lives and specific activities of 235U and 238U. Phys. Rev.4, 1889-1906], a value for λ¹⁸⁷Re of 1.6668 ± 0.0034 × 10⁻¹¹ a⁻¹ is determined. Using the λ²³⁸U value of Jaffey et al. (1971) and λ²³⁵U value of Schoene [Schoene B., Crowley J. L., Condon D. J., Schmitz M. D., and Bowring S. A. (2006) Reassessing the uranium decay constants for geochronology using ID-TIMS U-Pb data. Geochim. Cosmochim. Acta70, 426-445], a value for λ¹⁸⁷Re of 1.6689 ± 0.0031 × 10⁻¹¹ a⁻¹ is determined. These values are nominally higher (ca. 0.1 and ca. 0.2%) than the value determined by Smoliar et al. [Smoliar M. I., Walker R. J., and Morgan J. W. (1996) Re-Os isotope constraints on the age of Group IIA, IIIA, IVA, and IVB iron meteorites. Science271, 1099-1102], but within calculated uncertainty. Further refinement of λ¹⁸⁷Re by cross calibrating the molybdenite and U-Pb zircon chronometers should be possible by utilizing high precision, single-grain, chemical abrasion zircon U-Pb analyses.  相似文献   

Silicon isotopic fractionation of CAI-like vacuum evaporation residues     

Kim B. Knight  Noriko T. Kita  Frank M. Richter  Andrew M. Davis  John W. Valley 《Geochimica et cosmochimica acta》2009,73(20):6390-5891

Calcium-, aluminum-rich inclusions (CAIs) are often enriched in the heavy isotopes of magnesium and silicon relative to bulk solar system materials. It is likely that these isotopic enrichments resulted from evaporative mass loss of magnesium and silicon from early solar system condensates while they were molten during one or more high-temperature reheating events. Quantitative interpretation of these enrichments requires laboratory determinations of the evaporation kinetics and associated isotopic fractionation effects for these elements. The experimental data for the kinetics of evaporation of magnesium and silicon and the evaporative isotopic fractionation of magnesium is reasonably complete for Type B CAI liquids (Richter F. M., Davis A. M., Ebel D. S., and Hashimoto A. (2002) Elemental and isotopic fractionation of Type B CAIs: experiments, theoretical considerations, and constraints on their thermal evolution. Geochim. Cosmochim. Acta66, 521-540; Richter F. M., Janney P. E., Mendybaev R. A., Davis A. M., and Wadhwa M. (2007a) Elemental and isotopic fractionation of Type B CAI-like liquids by evaporation. Geochim. Cosmochim. Acta71, 5544-5564.). However, the isotopic fractionation factor for silicon evaporating from such liquids has not been as extensively studied. Here we report new ion microprobe silicon isotopic measurements of residual glass from partial evaporation of Type B CAI liquids into vacuum. The silicon isotopic fractionation is reported as a kinetic fractionation factor, α_Si, corresponding to the ratio of the silicon isotopic composition of the evaporation flux to that of the residual silicate liquid. For CAI-like melts, we find that α_Si = 0.98985 ± 0.00044 (2σ) for ²⁹Si/²⁸Si with no resolvable variation with temperature over the temperature range of the experiments, 1600-1900 °C. This value is different from what has been reported for evaporation of liquid Mg₂SiO₄ (Davis A. M., Hashimoto A., Clayton R. N., and Mayeda T. K. (1990) Isotope mass fractionation during evaporation of Mg₂SiO₄. Nature347, 655-658.) and of a melt with CI chondritic proportions of the major elements (Wang J., Davis A. M., Clayton R. N., Mayeda T. K., and Hashimoto A. (2001) Chemical and isotopic fractionation during the evaporation of the FeO-MgO-SiO₂-CaO-Al₂O₃-TiO₂-REE melt system. Geochim. Cosmochim. Acta65, 479-494.). There appears to be some compositional control on α_Si, whereas no compositional effects have been reported for α_Mg. We use the values of α_Si and α_Mg, to calculate the chemical compositions of the unevaporated precursors of a number of isotopically fractionated CAIs from CV chondrites whose chemical compositions and magnesium and silicon isotopic compositions have been previously measured.  相似文献   

LA-MC-ICPMS Pb-Pb dating of rutile from slowly cooled granulites: Confirmation of the high closure temperature for Pb diffusion in rutile   总被引：2，自引：0，他引：2  

Julie K. Vry  Joel A. Baker 《Geochimica et cosmochimica acta》2006,70(7):1807-1820

Rapid Pb-Pb dating of natural rutile crystals by laser ablation multiple-collector inductively coupled plasma mass spectrometry (LA-MC-ICPMS) is investigated as a tool for constraining geological temperature-time histories. LA-MC-ICPMS was used to analyse Pb isotopes in rutile from granulite-facies rocks from the Reynolds Range, Northern Territory, Australia. The resultant ages were compared with previous U-Pb zircon and monazite age determinations and new mica (muscovite, phlogopite, and biotite) Rb-Sr ages from the same metamorphic terrane. Rutile crystals ranging in size from 3.5 to 0.05 mm with ?20 ppm Pb were ablated with a 300-25 μm diameter laser beam. Crystals larger than 0.5 mm yielded sufficiently precise ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁷Pb/²⁰⁴Pb ratios to correct for the presence of common Pb, and individual rutile crystals often exhibited sufficient Pb isotopic heterogeneity to allow isochron calculations to be performed on replicate analyses of a single crystal. The mean of 12 isochron ages is 1544 ± 8 Ma (2 SD), with isochron ages for single crystals having uncertainties as low as ±1.3 Myr (2 SD). The ²⁰⁷Pb-²⁰⁶Pb ages calculated without correction for common Pb are typically <0.5% higher than the common-Pb-corrected isochron ages reflecting the very minor amounts of common Pb present in the rutile. The LA-MC-ICPMS method described samples only the outer 0.1-0.2 mm of the rutile crystals, resulting in a grain size-independent apparent closure temperature (T_c) for Pb diffusion in rutile that is less than the T_c of monazite ?0.1 mm in diameter, but significantly higher than the Rb-Sr system in muscovite (550 °C), phlogopite (435 °C) and biotite (400 °C). Even small rutile crystals are extremely resistant to isotopic resetting. For the established slow cooling rate of ca. 3 °C/Myr, the T_c for Pb diffusion in the analysed rutile is ca. 630 °C. This is in excellent agreement with recent experimental results that indicate that rutile has a higher T_c than previously thought (ca. 600-640 °C for rutile 0.1-0.2 mm diameter cooled at 3 °C/Myr; near 600 °C [Cherniak D.J., 2000. Pb diffusion in rutile. Contrib. Mineral. Petrol. 139, 198-207], versus 400 °C [Mezger, K., Hanson G.N., Bohlen S.R., 1989a. High precision U-Pb ages of metamorphic rutile: applications to the cooling history of high-grade terranes. Earth Planet. Sci. Lett. 96, 106-118.] for 1 °C/Myr), and with current T_c estimates for monazite and other high temperature geochronometers, which have been revised upwards in recent years. The new rutile ages, together with the other geochronological data from the region, support the interpretation that the Reynolds Range underwent prolonged slow cooling on a conductive geotherm, under nearly steady-state conditions. Slow cooling at ca. 3 °C/Myr persisted for at least 40 Myr followed the peak of high-T/low-P metamorphism to granulite-facies conditions, and probably continued at ca. 2-3 °C/Myr for ca. 200 Myr overall.  相似文献   

Isotopic anomalies of noble gases in meteorites and their origins—IV. C3 (Ornans) carbonaceous chondrites     

Leo Alaerts  Roy S Lewis  Edward Anders 《Geochimica et cosmochimica acta》1979,43(9):1421-1432

The C3O chondrites Kainsaz, Lancé and Ornans were studied by an acid dissolution technique, to characterize the noble-gas components in 3 mineral fractions: HF, HCl-solubles (99% of the meteorite), chromite and carbon (0.3–0.9%), and ‘phase Q’, a poorly characterized trace mineral (0.05–0.4%) containing most of the Ar, Kr, Xe. For all fractions, gas contents decline in the order Kainsaz > Lancé > Ornans; this trend parallels volatile contents but not heterogeneity of olivine composition or degree of metamorphism and seems to reflect progressively higher condensation temperatures from the solar nebula.Solubles contain nearly unfractionated Xe, and show ${}^{136}\text{Ar}{}^{132}\text{Xe}$ ratios up to 850. Hence the high $\text{Ar}\text{Xe}$ ratios (200–400) of bulk C3O chondrites must be due to an HF-soluble mineral (possibly magnetite). Phase Q contains ordinary planetary gases and a Ne component of ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{= 10.3 ± 0.4.}$Chromite and carbon contain Ne of ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{= 8.6 ± 0.1}$ and ‘CCF’ xenon (a peculiar component of possibly fissiogenic origin, enriched in the heavy isotopes but accompanied by a component enriched in the light isotopes).In all primitive chondrites, both the amount and the chemical separability of CCFXe parallel the abundance of promordial noble gases and other volatiles, such as C, N, Tl, Bi and In. The close correlation of CCFXe with various properties of undoubtedly local origin (volatile content, petrologic type, presence of ferrichromite and carbon, etc.) is more consistent with a local than with an extrasolar origin of this component. A volatile superheavy element seems to be the most plausible source, but the evidence is not conclusive.  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   

Further studies of trace elements in C3 chondrites     

H. Takahashi  Marie-Josée Janssens  John W. Morgan  Edward Anders 《Geochimica et cosmochimica acta》1978,42(1):97-106

Five carbonaceous chondrites (Renazzo C2V, Allende C3V, Omans C3O, Warrenton C3O, and Orgueil Cl) were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs. Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Te, Tl, U and Zn. These data, together with earlier measurements on seven additional C3 s, are interpreted in the light of pétrographie studies by MCSWEEN (1977a, b) and revised condensation temperatures (WAI and Wasson, 1977). Elements condensing between ~ 700 and 420 K (Se, Zn, S, Te, Br, In, Bi, Tl) are systematically more depleted than those condensing between 1000 and 900 K (Ge, Ag, Rb), by factors of 1.3 to 2, and the depletion correlates inversely with matrix content and directly with degree of metamorphism. The most plausible explanation appears to be a gas-dust fractionation during condensation, by settling of dust to the median plane of the nebula. In this model, gas/dust ratios relative to the cosmic ratio ranged from 0.7 at 1000 K to 0.5 at 700 K for those C3O s that accreted first (Ornans, Warrenton) and from 1.3 to 0.6 for the last (Kainsaz). There appears to have been no further gas/dust fractionation below 700 K.Abundances of Sb, Au and Cd follow earlier trends. Depletion of Sb and Au correlates with abundance of Fe-poor olivine and seems to reflect greater volatilization upon more prolonged or intense heating during chondrule formation. The 50–100-fold depletion of Cd in C3Os compared to C3Vs suggests condensation in a region where enough Fe was present to buffer the H₂S pressure.  相似文献   

Two oxygen isotopic components with extra-selenial origins observed among lunar metallic grains - In search for the solar wind component     

Ko Hashizume  Marc Chaussidon 《Geochimica et cosmochimica acta》2009,73(10):3038-1532

Oxygen isotopic analyses were performed in the surface layers of lunar metallic grains from lunar regolith samples 71501 and 79035, presumably exposed at the Moon surface at different times. We were able to reproduce the two extreme O components previously found [Hashizume K. and Chaussidon M. (2005) A non-terrestrial ¹⁶O-rich isotopic composition for the protosolar nebula. Nature434, 619-622; Ireland T. R., Holden P., Norman M. D. and Clarke J. (2006) Isotopic enhancements of ¹⁷O and ¹⁸O from solar wind particles in the lunar regolith. Nature440, 776-778], with a range observed of −12 ± 5 < Δ¹⁷O < +33 ± 3‰ (1σ). The relatively minor ¹⁶O-rich component corresponding to an end-member Δ¹⁷O value lower than −20‰ is likely the solar component. This comes from the fact that its concentration roughly agrees with the maximum solar wind abundance expected among the grains from the two samples. At variance the ¹⁶O-poor component is 5-10 times more abundant and thus likely non-solar. The δ¹⁸O range found for the ¹⁶O-poor component may reflect various processes such as isotope exchange reaction during oxidation of metallic iron and/or isotope fractionation by evaporation/condensation at the surface of the Moon or during implantation at depth in the lunar metallic grains. The present study suggests that planetary solid materials in bulk are systematically depleted in ¹⁶O relative to the solar isotopic composition, suggesting the existence of non-mass-dependent isotopic fractionations associated to the formation of solids in the accretion disk.  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   

The compositional classification of chondrites: III. Ungrouped carbonaceous chondrites     

Gregory W. Kallemeyn  John T. Wasson 《Geochimica et cosmochimica acta》1982,46(11):2217-2228

Seven carbonaceous chondrites (Allan Hills A77307, Adelaide, Al Rais, Coolidge, Grosnaja, Karoonda and Renazzo) with uncertain classifications were analyzed by instrumental and radiochemical neutron activation analysis for 29 elements: Na, Mg, Al, K, Ca, Sc, V, Cr, Mn, Fe, Co, Ni, Zn, Ga, Ge, As, Se, Br, Ru, Cd, Sb, La, Sm, Eu, Yb, Lu, Os, Ir and Au. Five of these chondrites (A77307, Adelaide, Al Rais, Karoonda and Renazzo) are unique ‘grouplets’, not closely related to other groups or to each other. Only Coolidge (CV4) and Grosnaja (CV3-an) are members of previously established groups. A77307 and Adelaide have refractory lithophile abundances similar to those in the CM-CO clan; A77307 probably is a member of that clan, but Adelaide, which shows CV-like petrographic characteristics, cannot as yet be assigned to a clan. Al Rais and Renazzo have similar refractory lithophile abundances (essentially at CI levels) and probably belong to the same clan, i.e., formed in the same region of the nebula. There are insufficient data to determine whether they formed at the same general region as the CI chondrites, but separates having O-isotope compositions near the terrestrial fractionation line indicate that this is plausible. Karoonda has refractory lithophile abundances ~ 1.21 × CI and appears to belong to a new clan distinct from CM-CO (1.11 × CI) and CV (1.34×).  相似文献   

Stable isotope records (δO and δC) of Lower-Middle Jurassic belemnites from the Western Balkan mountains (Bulgaria): Palaeoenvironmental application     

Lubomir Metodiev  Elena Koleva-Rekalova 《Applied Geochemistry》2008

Stable O and C isotope data of 110 Upper Pliensbachian-Lower Bajocian belemnites have been obtained and used to attempt a reconstruction of palaeotemperature and its variation in two epicontinental depositional environments from the Western Balkan mountains (Bulgaria). The samples were collected from 3 sections with high-resolution ammonite subdivision. Initially taphonomic, cathodoluminescence and geochemical analyses were used for evidence of diagenetic alteration. Non-luminescent parts of the belemnite rostra have been sampled for isotope analyses and 76 samples, having δ¹⁸O < −4‰ (PDB), δ¹³C > −0.5‰ (PDB), Fe < 250 ppm, Mn < 50 ppm, Sr > 950 ppm and Sr/Mn ratio > 80 were used for palaeotemperature interpretations. The O and C isotope data generally exhibit little stratigraphical variability with minor fluctuations, however, there are prominent positive C isotope excursions and coeval negative O isotope shifts detected in the Lower Toarcian Tenuicostatum, Falciferum and Bifrons Zones. The O isotope data, interpreted in terms of palaeotemperature, revealed relatively high seawater temperatures during the Toarcian, Aalenian and Early Bajocian, with detectable temperature rises during the Early Toarcian (maximum value of 29.6 °C). Both C isotope maxima and O isotope minima are used as evidence of the Early Toarcian anoxic event reported from many localities of the same age and in similar facies in Western Europe. In the study the latter is recognized as 3 episodes, which are closely related with the seawater temperature maxima. This isotope record pattern is considered as a consequence of a global Tethyan transgression during the Early Toarcian.  相似文献   

The thermal history of equilibrated ordinary chondrites and the relationship between textural maturity and temperature   总被引：1，自引：0，他引：1  

Ronit Kessel  John R. Beckett  Edward M. Stolper 《Geochimica et cosmochimica acta》2007,71(7):1855-1881

The compositions and textures of phases in eleven equilibrated ordinary chondrites from the H, L, and LL groups spanning petrographic types 4-6 were studied and used to constrain the thermal histories of their parent bodies. Based on Fe-Mg exchange between olivine and spinel, average equilibration temperatures for type 4-6 chondrites encompass a small range, 586-777 °C, relative to what is commonly assumed for peak temperatures (600-950 °C). The maximum temperatures recorded by individual chondrites, which are minima relative to peak metamorphic temperatures, increase subtly but systematically with metamorphic type and are tightly clustered for H4-6 (733-754 °C) and LL4-6 (670-777 °C). For the Ls, Ausson (L5) records a higher maximum olivine-spinel temperature (761 °C) than does the L4 chondrite Saratov (673 °C) or the L6 chondrite Glatton (712 °C). Our data combined with olivine-spinel equilibration temperatures calculated for other equilibrated ordinary chondrites using mineral compositions from the literature demonstrate that, in general, type 4 chondrites within each chemical group record temperatures lower than or equal to those of types 5-6 chondrites.For H chondrites, the olivine-spinel closure temperature is a function of spinel grain size, such that larger grains, abundant in types 5-6 chondrites, record temperatures of ∼740 °C or more while smaller grains, rare in types 5-6 but abundant in type 4 chondrites, record lower temperatures. Olivine-spinel temperatures in the type 6 chondrites Guareña and Glatton are consistent with rapid (50-100 °C/Myr) cooling from high temperatures in the ordinary chondrite parent bodies. With one exception (∼500 °C/Myr), olivine-spinel data for St.-Séverin (LL6) are consistent with similar cooling rates. Cooling rates of order 100 °C/Myr at ∼750 °C for type 6 chondrites are considerably higher than previously determined cooling rates for lower temperatures (?550 °C) based on metallography, fission tracks, and geochronology. For H chondrites, current thermal models of an “onion shell” parent body are inconsistent with a small range of peak temperatures based on olivine-spinel and two pyroxene thermometry combined with a wide dispersion of cooling rates at low temperatures. Equilibrated chondrites may have sampled regions near a major transition in physical properties such as near the base of a regolith pile.  相似文献   

Hemimorphite as a natural sink for arsenic in zinc deposits and related mine tailings: Evidence from single-crystal EPR spectroscopy and hydrothermal synthesis     

Mao Mao 《Geochimica et cosmochimica acta》2010,74(10):2943-2956

Hemimorphite is a refractory mineral in surface environments and occurs commonly in supergene non-sulfide Zn deposits and Zn mine tailings. Single-crystal electron paramagnetic resonance (EPR) spectra of gamma-ray-irradiated hemimorphite from Mapimi (Durango, Mexico) reveal two arsenic-associated oxyradicals: [AsO₄]⁴⁻ and [AsO₄]²⁻. Inductively coupled plasma mass spectrometry analyses confirm this sample to contain 270 ppm As and that hemimorphite from other Zn deposits has appreciable amounts of arsenic as well. Spin Hamiltonian parameters, including matrices g, A (⁷⁵As) and P(⁷⁵As), show that the [AsO₄]⁴⁻ radical formed from electron trapping by a locally uncompensated [AsO₄]³⁻ ion substituting for [SiO₄]⁴⁻. Matrices g, A(⁷⁵As) and P(⁷⁵As) of the [AsO₄]²⁻ radical show it to have the unpaired spin on the bridging oxygen of an [AsO₄]³⁻ ion at a Si site and linked to a monovalent impurity ion. This structural model for the [AsO₄]²⁻ radical is further supported by observed ²⁹Si and ¹H superhyperfine structures arising from interactions with a single Si atom (A/g_eβ_e = ∼1 mT at B//c) and two equivalent H atoms (A/g_eβ_e = ∼0.3 mT at B∧b = 10°), respectively. Hydrothermal experiments at 200 °C and ∼9.5 MPa show that hemimorphite contains up to ∼2.5 wt% As₂O₅ and suggest that both the arsenate concentration and the pH value in the solution affect the As content in hemimorphite. These results demonstrate that hemimorphite is capable of sequestering arsenate in its crystal lattice, hence is a natural sink for attenuating As in supergene non-sulfide Zn deposits and Zn mine tailings. Moreover, results from hemimorphite potentially have more far-reaching implications for major silicates such as zeolites in the immobilization and removal of arsenic in surface environments.  相似文献   

Evidence from Ar/Ar ages of lunar impact glasses for an increase in the impact rate ∼800 Ma ago     

N.E.B. Zellner  J.W. Delano  F. Barra  E. Olsen 《Geochimica et cosmochimica acta》2009,73(15):4590-7388

Geochemical and ⁴⁰Ar/³⁹Ar data on nine impact glasses from the Apollo 14, 16, and 17 landing sites indicate at least seven distinct impact events with ages ∼800 Ma. Rock fragments analyzed by Barra et al. [Barra F., Swindle T. D., Korotev R. L., Jolliff B. L., Zeigler R. A., and Olsen E. (2006) ⁴⁰Ar-³⁹Ar dating of Apollo 12 regolith: implications for the age of Copernicus and the source of nonmare materials, Geochim. Cosmochim. Acta,70, 6016-6031] from the Apollo 12 landing site and some Apollo 12 spherules reported by Levine et al. [Levine J., Becker T. A., Muller R. A., Renne P. R. (2005) ⁴⁰Ar/³⁹Ar dating of Apollo 12 impact spherules, Geophys. Res. Let., 32, L15201, doi: 10.1029/2005GL022874.] show ∼800 Ma ages, close to the accepted age of the Copernicus event, 800 ± 15 Ma [Bogard D. D., Garrison D. H., Shih C. Y., and Nyquist L. E. (1994) ³⁹Ar-⁴⁰Ar dating of two lunar granites: The age of Copernicus, Geochim. Cosmochim. Acta, 58, 3093-3100]. These Apollo 12 samples are thought to have been affected by material from the Copernicus event since there is a Copernicus ray going through the Apollo 12 landing site. When all of these data are viewed collectively, including an Apollo 16 glass bomb [Borchardt R., Stöffler D., Spettel B., Palme H. and Wänke H. (1986) Composition, structure, and age of the Apollo 16 subregolith basement as deduced from the chemistry of post-Imbrium melt bombs. In Proceedings, 17th Lunar and Planetary Science Conference, pp. E43-E54], and in the context of diverse compositional range and sample location, there is a suggestion that there may have been a transient increase in the global lunar impact flux at ∼800 Ma. Therefore, the Copernicus impact event could have been one of many. If correct, there should be evidence for this increased impact flux around 800 Ma ago in the age statistics of terrestrial impact samples.  相似文献   

Sorption and catalytic oxidation of Fe(II) at the surface of calcite   总被引：1，自引：0，他引：1  

Suzanne Mettler  Mariëtte Wolthers  Laurent Charlet 《Geochimica et cosmochimica acta》2009,73(7):1826-442

The effect of sorption and coprecipitation of Fe(II) with calcite on the kinetics of Fe(II) oxidation was investigated. The interaction of Fe(II) with calcite was studied experimentally in the absence and presence of oxygen. The sorption of Fe(II) on calcite occurred in two distinguishable steps: (a) a rapid adsorption step (seconds-minutes) was followed by (b) a slower incorporation (hours-weeks). The incorporated Fe(II) could not be remobilized by a strong complexing agent (phenanthroline or ferrozine) but the dissolution of the outmost calcite layers with carbonic acid allowed its recovery. Based on results of the latter dissolution experiments, a stoichiometry of 0.4 mol% Fe:Ca and a mixed carbonate layer thickness of 25 nm (after 168 h equilibration) were estimated. Fe(II) sorption on calcite could be successfully described by a surface adsorption and precipitation model (Comans & Middelburg, GCA51 (1987), 2587) and surface complexation modeling (Van Cappellen et al., GCA57 (1993), 3505; Pokrovsky et al., Langmuir16 (2000), 2677). The surface complex model required the consideration of two adsorbed Fe(II) surface species, >CO₃Fe⁺ and >CO₃FeCO₃H⁰. For the formation of the latter species, a stability constant is being suggested. The oxidation kinetics of Fe(II) in the presence of calcite depended on the equilibration time of aqueous Fe(II) with the mineral prior to the introduction of oxygen. If pre-equilibrated for >15 h, the oxidation kinetics was comparable to a calcite-free system (t_1/2 = 145 ± 15 min). Conversely, if Fe(II) was added to an aerated calcite suspension, the rate of oxidation was higher than in the absence of calcite (t_1/2 = 41 ± 1 min and t_1/2 = 100 ± 15 min, respectively). This catalysis was due to the greater reactivity of the adsorbed Fe(II) species, >CO₃FeCO₃H⁰, for which the species specific rate constant was estimated.  相似文献