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1.
Bulk chemical compositions of matrix material in Antarctic CM chondrites and other non-Antarctic CM and CI chondrites have been determined using microprobe defocused beam techniques. These are used, along with the results of previously published mineralogical studies, to provide mass balance constraints on the relative proportions of intergrown and intermixed phyllosilicate phases in carbonaceous chondrite matrices. Results of these calculations indicate differing amounts of PCP (a mixture of approximately 25% tochilinite and 75% cronstedtite) and serpentines (Mg-rich and Fe-rich varieties in varying proportions or intermediate compositional varieties). Additional sulfide phases are also probably necessary to account for excess Ni and S. Fe/Si ratios for matrices of individual meteorites range from 1.21 to 2.77, corresponding to PCP/(PCP + SERF) ratios of 0.16 to 0.58. Progressive aqueous alteration of matrix appears to have occurred by formation of tochilinite, then cronstedtite and Mg-rich serpentine, and finally Fe-rich serpentine and sulfides. CM matrix clearly did not behave as an isolated system during alteration. CI chondrite matrices appear to contain little if any PCP; this may be a natural consequence of the absence of chondrule-associated metal, from which PCP forms, in the unaltered precursor material. These data provide a more quantitative picture of low-temperature aqueous alteration processes in carbonaceous chondrite parent bodies than has heretofore been possible from TEM studies alone.  相似文献   

2.
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   

3.
A chrysotile-like phase, cronstedtite, polygonal serpentine, pentlandite, and finely intergrown tochilinite comprise the fine-grained rim (FGR) mineralogy of the Cold Bokkeveld CM chondrite. Transmission electron microscope images combined with compositional data indicate reaction among cronstedtite, the chrysotile-like phase, and polygonal serpentine. The Mg/(Mg+Fe) ratios of the cronstedtite are higher than those reported for the less altered Murchison CM chondrite. Cronstedtite grains exhibit layer separations, particularly at their boundaries.The FGRs surround different chondrule types but have similar bulk compositions and mineralogy. Ca is depleted in the FGRs relative to the bulk CM chondrite. The FGRs display non-uniform thicknesses, especially where they coat embayed chondrule areas, and they exhibit grain-size coarsening outward from the chondrules they enclose. FGR formation in Cold Bokkeveld is most plausibly explained by multiple accretionary episodes during which progressively coarser dust was deposited onto chondrules, presumably in the solar nebula. The compositional and mineralogic data are consistent with aqueous alteration on the parent body.  相似文献   

4.
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5.
A petrographic and electron microscopic study of the Mokoia CV3 carbonaceous chondrite shows that all of the chondrules and inclusions (>400 μm in diameter) and most of their fine-grained rims studied (referred to as chondrules/rims) contain various amounts of hydrous phyllosilicates (mostly saponite) formed by aqueous alteration of anhydrous silicates. The rims mainly consist of fine-grained olivine and saponite in varying proportions and contain crosscutting veins of Fe-rich olivine. The boundaries between the chondrules and their rims are irregular and show abundant evidence of aqueous alteration interactions between them. In contrast, the host matrix contains very minor amounts of saponite and shows no evidence of such extensive aqueous alteration. The boundaries between the chondrules/rims and the matrix are sharp and show no traces of the matrix having been involved in the alteration of the chondrules/rims. These observations indicate that the aqueous alteration in the chondrules/rims did not occur in the present setting.We suggest that the chondrules/rims are actually clasts transported from a location on the meteorite parent body different from where the Mokoia meteorite was from. The aqueous alteration of the chondrules/rims probably occurred there. The veins in the rims were originally fractures produced in an interchondrule matrix by impacts; these were later filled by Fe-rich olivine during aqueous activity. This location was then involved in impact brecciation, and individual chondrules were ejected as clasts with remnants of the matrix surrounding them. During the continuing brecciation, those chondrule/rim clasts were transported, mixed with anhydrous matrix grains, and finally lithified to the present meteorite. Therefore, the rims are fragmented remnants of a former matrix.Textures characterized by fine-grained rims surrounding chondrules in chondrites have been widely thought to have formed in the solar nebula before they accreted into their parent bodies. However, our results suggest that some textures may not be explained by such an accretionary model; instead, the multi-stage parent-body process modeled for the Mokoia rim formation may be a more plausible explanation.  相似文献   

6.
We have performed an experimental study of the aqueous alteration of the Allende CV3 carbonaceous chondrite under highly oxidizing conditions, in order to examine the alteration behavior of Allende’s anhydrous mineralogy. The experiments were carried out at temperatures of 100, 150, and 200 °C, for time periods between 7 and 180 days, with water/rock ratios ranging from 1:1 to 9:1. Uncrushed cubes of Allende were used so that the spatial relationships between reactant and product phases could be examined in detail. Scanning electron microscope studies show that in all the experiments, even those of short duration (7 days), soluble salts of Ca and Mg (CaSO4, CaCO3, and MgSO4) precipitated on the sample surface, indicating that these elements are rapidly mobilized during alteration. In addition, iron oxides and hydroxides formed on the sample surfaces. The sulfates, carbonates, and the majority of the iron-bearing secondary minerals are randomly distributed over the surface of samples. In some instances the iron oxides and hydroxides are constrained to the boundaries of altering mineral grains. Transmission electron microscope studies show that the FeO-rich olivine in the interior of the samples has altered to form interlayered serpentine/saponite and Fe-oxyhydroxides. The degree of alteration increases significantly with increasing water/rock ratio, and to a lesser extent with increasing duration of heating. The serpentine/saponite forms both by direct replacement of the olivine in crystallographically oriented intergrowths, and by recrystallization of an amorphous Si-rich phase that precipitates in pore space between the olivine grains. The alteration assemblage bears many similarities to those found in altered carbonaceous chondrites, although in detail there are important differences, which we attribute to (a) the relatively high temperatures of our experiments and (b) comparatively short reaction times compared with the natural examples. In terms of mineral assemblage, our experiments most closely resemble alteration in the CI chondrites, although the degree of alteration of our experiments is much lower. CI chondrites contain serpentine/saponite intergrowths and veins of Ca-sulfate and Ca-carbonate as well as the Fe-oxyhydroxide, ferrihydrite. However, the phyllosilicate phases formed in our experiments are somewhat coarser-grained than the finest phyllosilicate fraction present in CI chondrites, suggesting that alteration of the CI chondrites occurred at lower temperatures. In terms of mineral assemblage, our experiments also appear to come close to matching CR chondrites, although we infer that CR alteration probably occurred at temperatures <100 °C, based on the very fine-grained size of phyllosilicates in CR matrices.  相似文献   

7.
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   

8.
Petrographic, mineralogical and chemical analysis of naturally weathered equilibrated ordinary chondrites collected from ‘ hot’ deserts and Antarctica has revealed striking similarities and also pronounced differences in weathering between the two environments. Terrestrial weathering in all meteorites studied is dominated by oxidation and hydration of Fe,Ni metal, producing Fe-oxides and oxyhydroxides that have partially replaced the metal grains and have also occluded primary intergranular pores to form veins. Troilite weathers readily in ‘ hot’ desert environments but undergoes very little alteration under Antarctic conditions. Most of the primary porosity of ordinary chondrites has been occluded by the time that ∼ 15 to 25% of the initial Fe0 and Fe2+ has been oxidised to Fe3+ in both environments. Results from modelling the volume changes upon alteration of primary minerals to a range of weathering products demonstrates that the primary porosity of most meteorites is sufficient to accommodate weathering products. Dilation of primary pores and brecciation, which has been observed in parts of some meteorites, will only occur if the meteorite is especially metal-rich, or has a low primary porosity. These weathering products are absent from recent falls but have formed in a fall after ∼ 100 yr of museum storage.Cl-bearing akaganéite and hibbingite are common weathering products in Antarctic finds but occur in abundance in only one ‘ hot’ desert meteorite, Daraj 014. The majority of Fe-rich weathering products in meteorites from both environments contain low, but variable concentrations of Si, Mg and Ca. In most meteorites a proportion of these elements are inferred to be present as a very finely crystalline mineral with a ∼ 1.0-nm lattice fringe spacing; where seen within intragranular fractures this mineral has a topotactic relationship with olivine and orthopyroxene. In the heavily-weathered Antarctic finds ALHA 78045 and 77002, Si is concentrated in cronstedtite, a Fe-rich phyllosilicate. An unidentified hydrous Si-Fe-Ni-Mg mineral or gel has also partially replaced taenite in ALHA 78045. In addition to Fe-rich weathering products, ‘ hot’ desert meteorites contain sulphates, Ca-carbonate and silica, whereas such minerals are largely absent from Antarctic finds. The abundance of silicate weathering products in Antarctic meteorites is unexpected and indicates that olivine and pyroxene undergo significant chemical weathering in these environments. As preterrestrial cronstedtite is abundant in CM2 carbonaceous chondrites, the Antarctic environment may be a powerful analog for aqueous alteration in the asteroidal parent bodies of primitive meteorites.  相似文献   

9.
It appears that the highly unequilibrated Bishunpur ordinary chondrite preserves phase relations acquired during solar nebular processes to a relatively high degree; metamorphic temperatures may not have exceeded 300–350°C. The major categories of metal are: 3 kinds of metal in the metal matrix, three kinds in chondrule interiors and 2 kinds in chondrule rims. The fine-grained matrix metal is highly variable in composition: the kamacite Co content (7.8 ± 2.0 mg/g) is within the L-group range (6.7–8.2 mg/g) but extends well above and below; its Ni content (38 ± 5 mg/g) is considerably lower than in more equilibrated chondrites and taenite is Ni-rich ( > 450 mg/g) and unzoned. These compositions imply equilibration at very low temperatures of about 300–350°C. It seems unlikely that volume diffusion could account for the observed relatively unzoned phases; a better model involves mass transport by grain boundary diffusion and grain growth at the indicated temperatures. We find no evidence that the matrix was ever at higher temperatures. Large (50–650 μm) polycrystalline metal aggregates consisting of individually zoned crystals are also found in the matrix; they probably represent clusters formed in the solar nebula. A few large (50–250 μm) round monocrystalline grains are also present in the matrix.Metal-bearing chondrules tend to be highly reduced; they contain low-Ni metal that occasionally contains Si and/or Cr. Silicates in these chondrules tend to have low FeO(FeO + MgO) ratios. The Si-rich metal grains are never in contact with silicates and are always surrounded by troilite with a poorly characterized Ca, Cr-sulfide at the metal-troilite interface; they appear to be high temperature nebular condensates that avoided oxidation even during the chondrule forming process. Silicon contents drop below our detection limit when the sulfide coating is absent. Much more common in chondrule interiors are Si-free spheroidal metal grains not associated with sulfides. These have Ni and Co contents very similar to the Si-bearing grains, and appear to be oxidized variants of the same material. The third class of chondrule metal is fine ( ~1 μm) dusty grains inside individual olivine grains. These seem to reflect high temperature in situ reduction of FeO from the olivine.The composition of kamacite is different in sulfide-rich and sulfide-poor chondrule rims and in both cases it is dissimilar to the compositions in the chondrule interiors and matrix; this indicates that chondrule rims could not have resulted from reactions with the matrix, but are primary features acquired prior to accretton.  相似文献   

10.
Of the six chondrites that were listed as EH6 or EH6-an during the course of this study, we confirm the EH classification of Y-8404, Y-980211 and Y-980223 and the EH-an classification of Y-793225; two chondrites (A-882039 and Y-980524) are reclassified as EL (the former contains ferroan alabandite and both contain kamacite with ∼1 wt% Si). All of the meteorites contain euhedral enstatite grains surrounded by metal ± sulfide (although this texture is rare in Y-793225), consistent with enstatite crystallizing from a mixed melt. All contain enstatite with <0.04 wt% MnO; the three EH chondrites average 0.25 wt% Mn in troilite. (Literature data show that typical EH3-EH5 chondrites contain enstatite with 0.13-0.20 wt% MnO and troilite with 0.05-0.11 wt% Mn.) The three EH chondrites contain keilite [(Fe>0.5,Mg<0.5)S], which has been interpreted in the literature as a product of impact melting. Y-8404 and Y-980223 contain abundant silica (∼13 and ∼10 wt%, respectively), a rare phase in most enstatite chondrites. We suggest that all six meteorites have experienced impact melting; Mn was preferentially partitioned into sulfide during subsequent crystallization. The silica-rich samples may have become enriched in the aftermath of the impact by a redox reaction involving FeO and reduced Si. A-882039, Y-8404, Y-980211, Y-980223 and Y-980524 were incompletely melted; they contain rare relict chondrules and are classified as impact-melt breccias; Y-793225 is a chondrule-free impact-melt rock. If these EH and EH-an chondrites (which were previously listed as petrologic type 6) have, in fact, been impact melted, it seems plausible that collisional heating is generally responsible for EH-chondrite metamorphism. This is consistent with literature data showing that a large fraction (?0.7) of those chondrites classified EH5-7 and a significant fraction (?0.3) of those chondrites classified EH4 and EH4/5 possess textural and mineralogical properties suggestive of impact melting. In addition, ∼60% of classified EL6-7 chondrites (now including A-882039 and Y-980524) appear to have formed by impact melting. It thus seems likely that collisional heating is mainly responsible for EL- and EH-chondrite metamorphism.  相似文献   

11.
A set of troilite-silicate-metal (TSM) inclusions and chondrule rims in the Bishunpur (LL3.1) chondrite provide information regarding impact brecciation of small bodies in the early solar system. The TSM inclusions and chondrule rims consist of numerous angular to subrounded silicate grains that are individually enclosed by fine networks of troilite. FeNi metal also occurs in the troilite matrix. The silicates include olivine (Fo55-98), low-Ca pyroxene (En78-98), and high-Ca pyroxene (En48-68Wo11-32). Al- and Si-rich glass coexists with the silicates. Relatively coarse silicate grains are apparently fragments of chondrules typical of petrologic type-3 chondrites. Troilite fills all available cracks and pores in the silicate grains. Some of the TSM inclusions and rims are themselves surrounded by fine-grained silicate-rich rims (FGR).The TSM inclusions and rims texturally resemble the troilite-rich regions in the Smyer H-chondrite breccia. They probably formed by shock-induced mobilization of troilite during an impact event on a primitive asteroidal body. Because silicates in the TSM inclusions and rims have highly unequilibrated compositions, their precursor was presumably type-3 chondritic material like Bishunpur itself. The TSM inclusions and the chondrules with the TSM rims were fragmented and dispersed after the impact-induced compaction, then reaccreted onto the Bishunpur parent body. FGR probably formed around the TSM inclusions and rims, as well as around some chondrules, during the reaccumulation process. Components of most type-2 and 3 chondrites probably experienced similar processing, i.e., dispersal of unconsolidated materials and subsequent reaccumulation.  相似文献   

12.
A correlation of petrography, mineral chemistry and in situ oxygen isotopic compositions of fine-grained olivine from the matrix and of fine- and coarse-grained olivine from accretionary rims around Ca-Al-rich inclusions (CAIs) and chondrules in CV chondrites is used here to constrain the processes that occurred in the solar nebula and on the CV parent asteroid. The accretionary rims around Leoville, Vigarano, and Allende CAIs exhibit a layered structure: the inner layer consists of coarse-grained, forsteritic and 16O-rich olivine (Fa1-40 and Δ17O = −24‰ to −5‰; the higher values are always found in the outer part of the layer and only in the most porous meteorites), whereas the middle and the outer layers contain finer-grained olivines that are more fayalitic and 16O-depleted (Fa15-50 and Δ17O = −18‰ to +1‰). The CV matrices and accretionary rims around chondrules have olivine grains of textures, chemical and isotopic compositions similar to those in the outer layers of accretionary rims around CAIs. There is a correlation between local sample porosity and olivine chemical and isotopic compositions: the more compact regions (the inner accretionary rim layer) have the most MgO- and 16O-rich compositions, whereas the more porous regions (outer rim layers around CAIs, accretionary rims around chondrules, and matrices) have the most MgO- and 16O-poor compositions. In addition, there is a negative correlation of olivine grain size with fayalite contents and Δ17O values. However, not all fine-grained olivines are FeO-rich and 16O-poor; some small (<1 μm in Leoville and 5-10 μm in Vigarano and Allende) ferrous (Fa>20) olivine grains in the outer layers of the CAI accretionary rims and in the matrix show significant enrichments in 16O (Δ17O = −20‰ to −10‰). We infer that the inner layer of the accretionary rims around CAIs and, at least, some olivine grains in the finer portions of accretionary rims and CV matrices formed in an 16O-rich gaseous reservoir, probably in the CAI-forming region. Grains in the outer layers of the CAI accretionary rims and in the rims around chondrules as well as matrix may have also originated as 16O-rich olivine. However, these olivines must have exchanged O isotopes to variable extents in the presence of an 16O-poor reservoir, possibly the nebular gas in the chondrule-forming region(s) and/or fluids in the parent body. The observed trend in isotopic compositions may arise from mixtures of 16O-rich forsterites with grain overgrowths or newly formed grains of 16O-poor fayalitic olivines formed during parent body metamorphism. However, the observed correlations of chemical and isotopic compositions of olivine with grain size and local porosity of the host meteorite suggest that olivine accreted as a single population of 16O-rich forsterite and subsequently exchanged Fe-Mg and O isotopes in situ in the presence of aqueous solutions (i.e., fluid-assisted thermal metamorphism).  相似文献   

13.
The mineralogical and chemical characteristics of the fine-grained matrix (< or = 3 micrometers) of the unique primitive carbonaceous chondrite Acfer 094 have been investigated in detail by scanning electron microscopy (SEM) and analytical transmission electron microscopy (ATEM). Generally, the fine-grained matrix represents a highly unequilibrated assemblage of an amorphous material, small forsteritic olivines (200-300 nm), low Ca-pyroxenes (300-400 nm), and Fe,Ni-sulfides (100-300 nm). The matrix is basically unaffected by secondary processes. Only minor amounts of serpentine and ferrihydrite, as products of hydrous alteration, are present. Texturally, the amorphous material acts as a groundmass to olivines, pyroxenes, and sulfides, mostly exhibiting rounded or elongated morphologies. Only very few clastic mineral grains have been found. The texture and chemical composition of the amorphous material are consistent with an origin by disequilibrium condensation in either the cooling solar nebula or a circumstellar environment. As such, the amorphous material may be considered as a possible precursor of matrix materials in other types of chondrites. The non-clastic matrix olivines (Fo98-99) and pyroxenes (En97-100) are suggested to have formed either by condensation in the solar nebula under highly oxidizing conditions or by recrystallization from the amorphous material. The formation of these grains by fragmentation of chondrule components is unlikely due to chemical and microstructural reasons. Rapid cooling caused the observed intergrowths of clino/orthoenstatite in the Mg-rich matrix pyroxenes. Although some similarities exist comparing the fine-grained matrix of Acfer 094 with the matrices of the unequilibrated CO3 chondrite ALHA77307 and the unique type 3 chondrite Kakangari, Acfer 094 remains unique. Since it contains the highest measured concentrations of circumstellar SiC and the second highest of diamond (highest is Orgueil), it seems reasonable to suggested that at least parts of the amorphous material in the fine-grained matrix may be of circumstellar origin.  相似文献   

14.
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   

15.
The degrees of thermal metamorphism of 10 CM chondrites and of the Allende CV3 chondrite were evaluated from the viewpoint of “graphitization” of the carbonaceous macromolecular matter by means of flash pyrolysis-gas chromatography (GC). The unheated chondrites, Yamato- (Y-) 791198, Murray and Cold Bokkeveld, yielded larger amounts and wider varieties of pyrolyzates than the chondrites strongly heated in the parent asteroids, Y-82054, Y-86695, and Belgica- (B-) 7904, and Asuka- (A-) 881334 (more strongly heated than Y-793321, which has been weakly heated, but lesser than the other strongly heated meteorites). The weakly heated chondrites, Y-793321 and A-881458, showed intermediate features. The data indicate that graphitization of the carbonaceous matter is most extreme in the strongly heated chondrites and that during graphitization, the matter has lost its labile portion, which can generate pyrolyzates such as naphthalene. In order to establish a new method for the evaluation of the degree of graphitization of chondritic carbonaceous matter, a diagram was developed to show the relationship between the total amounts of pyrolyzates with retention times later than 5 min (=SRT>5) and the ratio of the amount of naphthalene, a pyrolysis product, to SRT>5 (=SN/SRT>5). The diagram indicates a possible evolutionary pathway of graphitization of the carbonaceous matter in carbonaceous chondrites.  相似文献   

16.
Linear saturated dicarboxylic acids are present in carbonaceous chondrite samples at concentrations that suggest aqueous alteration under conditions of metastable equilibrium. In this study, previously published values of dicarboxylic acid concentrations measured in Murchison, Yamato-791198, and Tagish Lake carbonaceous chondrites are converted to aqueous activities during aqueous alteration assuming water:rock ratios that range from 1:10 to 10:1. Logarithmic plots of the aqueous activities of any two dicarboxylic acids are proximal to lines whose slope is fixed by the stoichiometry of reactions describing the oxidation-reduction equilibrium between the two species. The precise position of any line is controlled by the equilibrium constant of the reaction relating the species and the hydrogen fugacity for the reaction of interest. Reactions among succinic (C4), glutaric (C5), and adipic (C6) acids obtained from CM2 chondrites show evidence of metastable equilibrium and yield values that agree to within 0.3 log units at 298.15 K and 0.6 log units at 473.15 K. At a water:rock ratio of 1:1, metastable equilibrium among succinic, glutaric, and adipic acids results in calculated values during aqueous alteration that range from −6.2 at 298.15 K to −3.3 at 373.15 K. These values are consistent with those obtained in previous work on carbonaceous chondrites and with metastable equilibrium at temperatures ranging from 300 to 355 K in contact with cronstedtite + magnetite.  相似文献   

17.
Tochilinite and tochilinite-serpentine-intergrowth (TSI) phases, including their nanotubes, are major components of CM carbonaceous chondrites. The laboratory synthesis of tochilinite and TSI phases, particularly their nanotubular forms, has rarely been reported. In this article, we show that FeMgAl tochilinite nanotubes and TSI nanotubes can be hydrothermally prepared from heat-treated metal particle mixtures below 200 °C under reducing and basic conditions. The metal particles used in the preparation of FeMgAl tochilinite were Fe, Mg and Al and those used for the preparation of TSI were Fe, Mg, Al, Si, Cr and Ni. FE-SEM, TEM, HRTEM, ED, EDX and XRD were used to characterize the reaction products. The yield of FeMgAl tochilinite and TSI was generally low and the FeMgAl tochilinite and TSI samples were very heterogeneous. Both the FeMgAl tochilinite and TSI crystallites existed in two forms, i.e. flakes and nanotubes. They generally had micrometer to sub-micrometer sizes and low crystallinity, and they were extremely sensitive to the electron beam. The FeMgAl tochilinite showed various structural modifications; however, the chemical compositions of these structural modifications were similar. The same phenomenon existed for TSI. The structural modifications of FeMgAl tochilinite and TSI may originate mainly from their mixed-layer structures, two-dimensional incommensurability of their sub-structures and the synthetic conditions. Some of the FeMgAl tochilinite nanotubes and the TSI nanotubes were likely to have been formed by curling of the corresponding flakes. The curling process appears to be delicate, requiring a quiet reaction environment with stable temperature and pressure and without vibrations. Our synthetic FeMgAl tochilinite and TSI showed remarkable similarities to natural tochilinite and TSI, respectively. Therefore, meteoritic tochilinite and TSI probably formed by reaction of metal particles with S2− bearing water at temperatures of around 50-100 °C.  相似文献   

18.
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   

19.
CM chondrites are aqueously altered rocks that contain ∼9 wt% H2O+ (i.e., indigenous water) bound in phyllosilicates; also present are clumps of serpentine-tochilinite intergrowths (previously called “poorly characterized phases” or PCP), pentlandite and Ni-bearing pyrrhotite. We studied 11 CM chondrites that span the known range from least altered to most altered. We used various petrologic properties (many previously identified) that provide information regarding the degree of aqueous alteration. There are no known unaltered or slightly altered CM chondrites (e.g., rocks containing numerous chondrules with primary igneous glass). Some CM properties result from processes associated with early and intermediate stages of the alteration sequence (i.e., hydration of matrix, alteration of chondrule glass, and production of large PCP clumps). Other petrologic properties reflect processes active throughout the alteration sequence; these include oxidation of metallic Fe-Ni, alteration of chondrule phenocrysts, changes in PCP composition (reflecting an increase in the phyllosilicate/sulfide ratio), and changes in carbonate mineralogy (reflecting the development of dolomite and complex carbonates at the expense of Ca carbonate).On the basis of these parameters, we propose a numerical alteration sequence for CM chondrites. Because there are no known CM samples that display only incipient alteration, the least altered sample was arbitrarily assigned to subtype 2.6. The most altered CM chondrites, currently classified CM1, are assigned to subtype 2.0. These highly altered rocks have essentially no mafic silicates; they contain chondrule pseudomorphs composed mainly of phyllosilicate. However, their bulk compositions are CM-like, and they are closer in texture to other C2 chondrites than to CI1 chondrites (which lack chondrule pseudomorphs). Using several diagnostic criteria, we assigned petrologic subtypes (±0.1) to every CM chondrite in our study: QUE 97990, CM2.6; Murchison, CM2.5; Kivesvaara, CM2.5; Murray, CM2.4/2.5; Y 791198, CM2.4; QUE 99355, CM2.3; Nogoya, CM2.2; Cold Bokkeveld, CM2.2; QUE 93005, CM2.1; LAP 02277, CM2.0; MET 01070, CM2.0.The proposed CM numerical alteration sequence improves upon the existing scheme of Browning et al. (1996) in that it does not require a complicated algorithm applied to electron-microprobe data to determine the average matrix phyllosilicate composition. The new sequence is more comprehensive and employs petrologic subtypes that are easier to use and remember than mineralogic alteration index values.New neutron-activation analyses of QUE 97990, QUE 93005, MET 01070, Murchison and Crescent, together with literature data, confirm the compositional uniformity of the CM group; different degrees of alteration among CM chondrites do not lead to resolvable bulk compositional differences. This suggests that the textural differences among individual CM chondrites reflect progressive alteration of similar hypothetical CM3.0 starting materials in different regions of the same parent body, with minimal aqueous transport of materials over appreciable (e.g., meters) distances.  相似文献   

20.
Amoeboid olivine aggregates (AOAs) are the most common type of refractory inclusions in CM, CR, CH, CV, CO, and ungrouped carbonaceous chondrites Acfer 094 and Adelaide; only one AOA was found in the CBb chondrite Hammadah al Hamra 237 and none were observed in the CBa chondrites Bencubbin, Gujba, and Weatherford. In primitive (unaltered and unmetamorphosed) carbonaceous chondrites, AOAs consist of forsterite (Fa<2), Fe, Ni-metal (5-12 wt% Ni), and Ca, Al-rich inclusions (CAIs) composed of Al-diopside, spinel, anorthite, and very rare melilite. Melilite is typically replaced by a fine-grained mixture of spinel, Al-diopside, and ±anorthite; spinel is replaced by anorthite. About 10% of AOAs contain low-Ca pyroxene replacing forsterite. Forsterite and spinel are always 16O-rich (δ17,18O∼−40‰ to −50‰), whereas melilite, anorthite, and diopside could be either similarly 16O-rich or 16O-depleted to varying degrees; the latter is common in AOAs from altered and metamorphosed carbonaceous chondrites such as some CVs and COs. Low-Ca pyroxene is either 16O-rich (δ17,18O∼−40‰) or 16O-poor (δ17,18O∼0‰). Most AOAs in CV chondrites have unfractionated (∼2-10×CI) rare-earth element patterns. AOAs have similar textures, mineralogy and oxygen isotopic compositions to those of forsterite-rich accretionary rims surrounding different types of CAIs (compact and fluffy Type A, Type B, and fine-grained, spinel-rich) in CV and CR chondrites. AOAs in primitive carbonaceous chondrites show no evidence for alteration and thermal metamorphism. Secondary minerals in AOAs from CR, CM, and CO, and CV chondrites are similar to those in chondrules, CAIs, and matrices of their host meteorites and include phyllosilicates, magnetite, carbonates, nepheline, sodalite, grossular, wollastonite, hedenbergite, andradite, and ferrous olivine.Our observations and a thermodynamic analysis suggest that AOAs and forsterite-rich accretionary rims formed in 16O-rich gaseous reservoirs, probably in the CAI-forming region(s), as aggregates of solar nebular condensates originally composed of forsterite, Fe, Ni-metal, and CAIs. Some of the CAIs were melted prior to aggregation into AOAs and experienced formation of Wark-Lovering rims. Before and possibly after the aggregation, melilite and spinel in CAIs reacted with SiO and Mg of the solar nebula gas enriched in 16O to form Al-diopside and anorthite. Forsterite in some AOAs reacted with 16O-enriched SiO gas to form low-Ca pyroxene. Some other AOAs were either reheated in 16O-poor gaseous reservoirs or coated by 16O-depleted pyroxene-rich dust and melted to varying degrees, possibly during chondrule formation. The most extensively melted AOAs experienced oxygen isotope exchange with 16O-poor nebular gas and may have been transformed into magnesian (Type I) chondrules. Secondary mineralization and at least some of the oxygen isotope exchange in AOAs from altered and metamorphosed chondrites must have resulted from alteration in the presence of aqueous solutions after aggregation and lithification of the chondrite parent asteroids.  相似文献   

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