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1.
Abstract— The fine-grained matrix of the unique, unequilibrated carbonaceous chondrite Lewis Cliff (LEW) 85332 has been studied by scanning electron microscopy (SEM), electron probe microanalysis (EPMA) and transmission electron microscopy (TEM). Compositionally, LEW 85332 has a matrix that is more Fe-rich than typical CI chondrites but has elemental abundance ratios that appear to be closer to CI matrices than to CM or CR chondrites. The mineralogy of the matrix is dominated by phyllosilicate phases that are predominantly interlayered Fe-rich serpentine/saponite; anhydrous silicate phases such as olivine and pyroxene are rare. Minor magnetite, troilite and ferrihydrite also occur associated with the phyllosilicates. Despite the high degree of weathering in LEW 85332, the phyllosilicates appear to have an extraterrestrial origin, but the highly variable Mg/Fe ratios of saponite may be the result of partial terrestrial oxidation of Fe-rich saponite to a more Mg-rich saponite and ferrihydrite. Alternatively, some of the ferrihydrite may have formed as a result of terrestrial weathering of Fe-Ni metal. The compositional and mineralogical data suggest that the matrix of LEW 85332 may represent a very early stage in the type of aqueous alteration experienced by the CI chondrites, although it is improbable that LEW 85332 was a precursor to the CI chondrites because of its high abundance of chondrules. The absence of carbonates, the high-Fe content of the matrix and phyllosilicate phases and relatively low abundance of magnetite all indicate that the degree of oxidation and leaching of LEW 85332 matrix was significantly less than that experienced by the CI chondrites. The absence of clear evidence for alteration of chondrules suggests that either the formation of the hydrous phases in the matrix occurred prior to accretion or that alteration occurred on a parent body and involved limited amounts of fluid, such that the reactions took place preferentially and exclusively within the fine-grained (anhydrous?) matrix materials.  相似文献   

2.
We investigated the petrologic, geochemical, and spectral parameters that relate to the type and degree of aqueous alteration in nine CM chondrites and one CI (Ivuna) carbonaceous chondrite. Our underlying hypothesis is that the position and shape of the 3 μm band is diagnostic of phyllosilicate mineralogy. We measured reflectance spectra of the chondrites under dry conditions (elevated temperatures) and vacuum (10?8 to 10?7 torr) to minimize adsorbed water and mimic the space environment, for subsequent comparison with reflectance spectra of asteroids. We have identified three spectral CM groups in addition to Ivuna. “Group 1,” the least altered group as determined from various alteration indices, is characterized by 3 μm band centers at longer wavelengths, and is consistent with cronstedtite (Fe‐serpentine). “Group 3,” the most altered group, is characterized by 3 μm band centers at shorter wavelengths and is consistent with antigorite (serpentine). “Group 2” is an intermediate group between group 1 and 3. Ivuna exhibits a unique spectrum that is distinct from the CM meteorites and is consistent with lizardite and chrysotile (serpentine). The petrologic and geochemical parameters, which were determined using electron microprobe analyses and microscopic observations, are found to be consistent with the three spectral groups. These results indicate that the distinct parent body aqueous alteration environments experienced by these carbonaceous chondrites can be distinguished using reflectance spectroscopy. High‐quality ground‐based telescopic observations of Main Belt asteroids can be expected to reveal not just whether an asteroid is hydrated, but also details of the alteration state.  相似文献   

3.
The CM carbonaceous chondrite meteorites experienced aqueous alteration in the early solar system. They range from mildly altered type 2 to almost completely hydrated type 1 chondrites, and offer a record of geochemical conditions on water‐rich asteroids. We show that CM1 chondrites contain abundant (84–91 vol%) phyllosilicate, plus olivine (4–8 vol%), magnetite (2–3 vol%), Fe‐sulfide (<5 vol%), and calcite (<2 vol%). The CM1/2 chondrites contain phyllosilicate (71–88 vol%), olivine (4–20 vol%), enstatite (2–6 vol%), magnetite (2–3 vol%), Fe‐sulfides (1–2 vol%), and calcite (~1 vol%). As aqueous alteration progressed, the abundance of Mg‐serpentine and magnetite in the CM chondrites increased. In contrast, calcite abundances in the CM1/2 and CM1 chondrites are often depleted relative to the CM2s. The modal data support the model, whereby metal and Fe‐rich matrix were the first components to be altered on the CM parent body(ies), before further hydration attacked the coarser Mg‐rich silicates found in chondrules and fragments. Based on the absence of tochilinite, we suggest that CM1 chondrites experienced increased alteration due to elevated temperatures (>120 °C), although higher water/rock ratios may also have played a role. The modal data provide constraints for interpreting the composition of asteroids and the mineralogy of samples returned from these bodies. We predict that “CM1‐like” asteroids, as has been proposed for Bennu—target for the OSIRIS‐REx mission—will have a high abundance of Mg‐rich phyllosilicates and Fe‐oxides, but be depleted in calcite.  相似文献   

4.
Here, we present the results of a multitechnique study of the bulk properties of insoluble organic material (IOM) from the Tagish Lake meteorite, including four lithologies that have undergone different degrees of aqueous alteration. The IOM C contents of all four lithologies are very uniform and comprise about half the bulk C and N contents of the lithologies. However, the bulk IOM elemental and isotopic compositions vary significantly. In particular, there is a correlated decrease in bulk IOM H/C ratios and δD values with increasing degree of alteration—the IOM in the least altered lithology is intermediate between CM and CR IOM, while that in the more altered lithologies resembles the very aromatic IOM in mildly metamorphosed CV and CO chondrites, and heated CMs. Nuclear magnetic resonance (NMR) spectroscopy, C X‐ray absorption near‐edge (XANES), and Fourier transform infrared (FTIR) spectroscopy confirm and quantitate this transformation from CR‐like, relatively aliphatic IOM functional group chemistry to a highly aromatic one. The transformation is almost certainly thermally driven, and probably occurred under hydrothermal conditions. The lack of a paramagnetic shift in 13C NMR spectra and 1s‐σ* exciton in the C‐XANES spectra, both typically seen in metamorphosed chondrites, shows that the temperatures were lower and/or the timescales were shorter than experienced by even the least metamorphosed type 3 chondrites. Two endmember models were considered to quantitatively account for the changes in IOM functional group chemistry, but the one in which the transformations involved quantitative conversion of aliphatic material to aromatic material was the more successful. It seems likely that similar processes were involved in producing the diversity of IOM compositions and functional group chemistries among CR, CM, and CI chondrites. If correct, CRs experienced the lowest temperatures, while CM and CI chondrites experienced similar more elevated temperatures. This ordering is inconsistent with alteration temperatures based on mineralogy and O isotopes.  相似文献   

5.
We have carried out a SEM-EPMA-TEM study to determine the textures and compositions of relict primary iron sulfides and their alteration products in a suite of moderately to heavily altered CM1 carbonaceous chondrites. We observed four textural groups of altered primary iron sulfides: (1) pentlandite+phyllosilicate (2P) grains, characterized by pentlandite with submicron lenses of phyllosilicates; (2) pyrrhotite+pentlandite+magnetite (PPM) grains, characterized by pyrrhotite–pentlandite exsolution textures with magnetite veining and secondary pentlandite; (3) pentlandite+serpentine (PS) grains, characterized by relict pentlandite exsolution, serpentine, and secondary pentlandite; and (4) pyrrhotite+pentlandite+magnetite+serpentine (PPMS) grains, characterized by features of both the PPM and PS grains. We have determined that all four groups were initially primary iron sulfides, which formed from crystallization of immiscible sulfide melts within silicate chondrules in the solar nebula. The fact that such different alteration products could result from the same precursor sulfides within even the same meteorite sample further underscores the complexity of the aqueous alteration environment for the CM chondrites. The different alteration reactions for each textural group place constraints on the mechanisms and conditions of alteration with evidence for acidic environments, oxidizing environments, and changing fluid compositions (Ni-bearing and Si-Mg-bearing).  相似文献   

6.
Abstract— In most groups of carbonaceous chondrites, minerals occur that are formed due to aqueous alteration in the nebula and/or within meteorite parent bodies. For determining the evolution of materials in the early solar system, it is of significant importance to clearly identify evidence for either nebular or planetary aqueous alteration. Therefore, results from the study of chondrites have fundamental implications for ideas concerning nebular dynamics, gas-solid interactions in the nebula, and accretionary processes. Considering the topic of this review, it is important to define nebular and parent body processes. The solar nebula activity should include condensation processes of high- and low-temperature components as well as processes of chemical fractionation and grain-size sorting, mixing of solids and gas, and interactions between early formed solids with the remaining gas; but it should exclude processes that occurred in small uncompacted protoplanetary objects that may have been totally destroyed again before accretion of the final meteorite parent bodies. Therefore, the term “preaccretionary” instead of “nebula” is used in this paper to include all these processes that may have occurred in small precursor planetesimals. Currently, there is no doubt that parent body aqueous alteration is a fundamental process in the evolution of several groups of carbonaceous chondrites. However, due to textural and mineralogical observations and chemical analyses, strong arguments have been found also indicating preaccretionary aqueous alteration of distinct components in carbonaceous chondrites. In this paper, evidence for preaccretionary aqueous alteration in carbonaceous chondrites and their components taken from previous studies is discussed in detail. The strongest evidence for preaccretionary alteration comes from studies of CM chondrites. The survival of highly unequilibrated mineral assemblages in accretionary rims, and sharp contacts between chondrule glass and surrounding phyllosilicates, are only two important arguments for preaccretionary alteration features among many others discussed in the paper. Similar observations were also made in CR, CH and related chondrites. Due to the small abundance of water-bearing phases in CO and CV chondrites, the origin of phyllosilicates in these groups is less clear. A preaccretionary origin of hydrous phases in Ca-Al-rich inclusions (CAIs) has also been suggested by several scientists. In CI chondrites, no strong indications for such processes have been found, mainly due to heavy brecciation and severe parent body alteration.  相似文献   

7.
Abstract— The oxidized CV3 chondrites can be divided into two major subgroups or lithologies, Bali-like (CV3oxB) and Allende-like (CV3oxA), in which chondrules, calcium-aluminum-rich inclusions (CAIs) and matrices show characteristic alteration features (Weisberg et al, 1997; Krot et al, 1997d; Kimura and Ikeda, 1997). The CV3oxB lithology is present in Bali, Kaba, parts of the Mokoia breccia and, possibly, in Grosnaja and Allan Hills (ALH) 85006. It is characterized by the presence of the secondary low-Ca phyllosilicates (saponite and sodium phlogopite), magnetite, Ni-rich sulfides, fayalite (Fa>90), Ca-Fe-rich pyroxenes (Fs10–50Wo45–50) and andradite. Phyllosilicates replace primary Ca-rich minerals in chondrules and CAIs, which suggests mobilization of Ca during aqueous alteration. Magnetite nodules are replaced to various degrees by fayalite, Ca-Fe-rich pyroxenes and minor andradite. Fayalite veins crosscut fine-grained rims around chondrules and extend into the matrix. Thermodynamic analysis of the observed reactions indicates that they could have occurred at relatively low temperatures (<300 °C) in the presence of aqueous solutions. Oxygen isotopic compositions of the coexisting magnetite and fayalite plot close to the terrestrial fractionation line with large Δ18Ofayalite-magnetite fractionation (～20%). We infer that phyllosilicates, magnetite, fayalite, Ca-Fe-rich pyroxenes and andradite formed at relatively low temperatures (<300 °C) by fluid-rock interaction in an asteroidal environment. Secondary fayalite and phyllosilicates are virtually absent in chondrules and CAIs in the CV3oxA lithology, which is present in Allende and its dark inclusions, Axtell, ALHA81258, ALH 84028, Lewis Cliff (LEW) 86006, and parts of the Mokoia and Vigarano breccias. Instead secondary nepheline, sodalite, and fayalitic olivine are common. Fayalitic olivine in chondrules replaces low-Ca pyroxenes and rims and veins forsterite grains; it also forms coarse lath-shaped grains in matrix. Secondary Ca-Fe-rich pyroxenes are abundant. We infer that the CV3oxA lithology experienced alteration at higher temperatures than the CV3oxB lithology. The presence of the reduced and CV3oxA lithologies in the Vigarano breccia and CV3oxA and CV3oXB lithologies in the Mokoia breccia indicates that all CV3 chondrites came from one heterogeneously altered asteroid. The metamorphosed clasts in Mokoia (Krot and Hutcheon, 1997) may be rare samples of the hotter interior of the CV asteroid. We conclude that the alteration features observed in the oxidized CV3 chondrites resulted from the fluid-rock interaction in an asteroid during progressive metamorphism of a heterogeneous mixture of ices and anhydrous materials mineralogically similar to the reduced CV3 chondrites.  相似文献   

8.
Abstract— Small particles 200 μm in diameter from the hydrous carbonaceous chondrites Orgueil CI, Murchison CM2, and Tagish Lake were experimentally heated for short durations at subsolidus temperatures under controlled ambient pressures in order to examine the bulk mineralogical changes of hydrous micrometeorites during atmospheric entry. The three primitive meteorites consist mainly of various phyllosilicates and carbonates that are subject to decomposition at low temperatures, and thus the brief heating up to 1000 °C drastically changed the mineralogy. Changes included shrinkage of interlayer spacing of saponite due to loss of molecular water at 400–600 °C, serpentine and saponite decomposition to amorphous phases at 600 and 700 °C, respectively, decomposition of Mg‐Fe carbonate at 600 °C, recrystallization of secondary olivine and Fe oxide or metal at 700–800 °C, and recrystallization of secondary low‐Ca pyroxene at 800 °C. The ambient atmospheric pressures controlled species of secondary Fe phase: taenite at pressures lower than 10?2 torr, magnesiowüstite from 10?3 to 10?1 torr, and magnetite from 10?2 to 1 torr. The abundance of secondary low‐Ca pyroxene increases in the order of Murchison, Orgueil, and Tagish Lake, and the order corresponds to saponite abundance in samples prior to heating. Mineralogy of the three unmelted micrometeorites F96CI024, kw740052, and kw740054 were investigated in detail in order to estimate heating conditions. The results showed that they might have come from different parental objects, carbonaterich Tagish Lake type, carbonate‐poor Tagish Lake or CI type, and CM type, respectively, and experienced different peak temperatures, 600, 700, and 800?900 °C, respectively, at 60–80 km altitude upon atmospheric entry.  相似文献   

9.
Abstract— Twenty-two carbonaceous chondrite clasts from the two howardites Bholghati and EET87513 were analyzed. Clast N from EET87513 is a fragment classified as CM2 material on the basis of texture, bulk composition, mineralogy, and bulk O isotopic composition. Carbonaceous chondrite clasts from Bholghati, for which less data are available because of their small size, can be divided into two petrologic types: C1 and C2. C1 clasts are composed of opaque matrix with rare coarse-grained silicates as individual mineral fragments; textures resemble CI meteorites and some dark inclusions from CR meteorites. Opaque matrix is predominantly composed of flaky saponite; unlike typical CI and CR meteorites, serpentine is absent in the samples we analyzed. C2 clasts contain chondrules, aggregates, and individual fragments of coarse-grained silicates in an opaque matrix principally composed of saponite and anhydrous ferromagnesian silicates with flaky textures similar to phyllosilicates. These anhydrous ferromagnesian silicates are interpreted as the product of heating of pre-existing serpentine. The carbonaceous chondrite clasts we have studied from these two howardites are, with one notable exception (clast N from EET87513), mineralogically distinct from typical carbonaceous chondrites. However, these clasts have very close affinities to carbonaceous chondrites and have also experienced thermal metamorphism and aqueous alteration, but to different degrees.  相似文献   

10.
Abstract— Iron‐rich aureoles in CM carbonaceous chondrites are previously unidentified domains of aqueously altered matrix material, whose FeO content may exceed that of the surrounding matrix by up to more than 15 wt%. We describe the petrography and mineralogy of these objects in the CM chondrites Murray, Murchison, and Allan Hills (ALH) 81002. The size of Fe‐rich aureoles ranges from a few hundred microns to several millimeters in diameter and appears to be a function of the degree of alteration of the host chondrite. The origin of Fe‐rich aureoles is related to the alteration of large metal grains that has resulted in the formation of characteristic PCP‐rich reaction products that are frequently observed at the centers of the aureoles. This suggests that Fe‐rich aureoles in CM chondrites are the result of the mobilization of Fe from altering metal grains into the matrix. The fact that Fe‐rich aureoles enclose numerous chondritic components such as chondrules, calcium‐aluminum‐rich inclusions (CAIs), and mineral fragments, as well as their radial symmetric appearance, are strong evidence that they formed in situ and that significant directional fluid flow was not involved in the alteration process. This and additional constraints, such as the distribution of S and other elements, as well as the inferred alteration conditions, are consistent with in situ parent‐body alteration. The observations are, however, entirely incompatible with preaccretionary alteration models in which the individual CM chondrite components have experienced diverse alteration histories. The presence of numerous intact aureoles in the brecciated CM chondrites Murray and Murchison further suggests that the alteration occurred largely after brecciation affected these meteorites. Therefore, the progressive aqueous alteration of CM chondrites may not be necessarily coupled to brecciation as has been previously proposed.  相似文献   

11.
Abstract– Eight saponite‐rich micrometeorites with very similar mineralogy were found from the recent surface snow in Antarctica. They might have come to Earth as a larger meteoroid and broke up into pieces on Earth, because they were recovered from the same layer and the same location of the snow. Synchrotron X‐ray diffraction (XRD) analysis indicates that saponite, Mg‐Fe carbonate, and pyrrhotite are major phases and serpentine, magnetite, and pentlandite are minor phases. Anhydrous silicates are entirely absent from all micrometeorites, suggesting that their parental object has undergone heavy aqueous alteration. Saponite/serpentine ratios are higher than in the Orgueil CI chondrite and are similar to the Tagish Lake carbonaceous chondrite. Transmission electron microscope (TEM) observation indicates that serpentine occupies core regions of fine‐grained saponite, pyrrhotite has a low‐Ni concentration, and Mg‐Fe carbonate shows unique concentric ring structures and has a mean molar Mg/(Mg + Fe) ratio of 0.7. Comparison of the mineralogy to hydrated chondrites and interplanetary dust particles (IDPs) suggests that the micrometeorites are most similar to the carbonate‐poor lithology of the Tagish Lake carbonaceous chondrite and some hydrous IDPs, but they show a carbonate mineralogy dissimilar to any primitive chondritic materials. Therefore, they are a new variant of saponite‐rich micrometeorite extracted from a primitive hydrous asteroid and recently accreted to Antarctica.  相似文献   

12.
Abstract– CM chondrites are primitive solar‐system materials that have undergone high degrees of aqueous alteration, resulting in the formation of secondary minerals including carbonates. Two different carbonate minerals (calcite/aragonite and dolomite) together constitute 1.4–2.8 vol% of CM chondrites. In contrast, CI chondrites contain four different carbonate minerals: calcite/aragonite, dolomite, breunnerite, and siderite. CI chondrites have abundant dolomite, a mineral that seems to be absent in the most aqueously altered CM chondrites. In this study, carbonates in seven CM chondrites (Y‐791198, LaPaz Icefield 04796, Cold Bokkeveld, Nogoya, Queen Alexandra Range 93005, Allan Hills 83100, and Meteorite Hills 01070) were studied petrographically and by electron microprobe. The results indicate that carbonate formation in CM chondrites differs from that in CI chondrites and is more complex than previously recognized. Our studies of CM chondrites indicate that (1) carbonates formed on the parent asteroid in an aqueous environment that gradually changed in composition, (2) at some stage, Ca and Mg activities in the environment were high enough to form metastable dolomite, and (3) dolomites disappeared in the most aqueously altered CM chondrites.  相似文献   

13.
Tochilinite/cronstedtite intergrowths are commonly observed as alteration products in CM chondrite matrices, but the conditions under which they formed are still largely underconstrained due to their scarcity in terrestrial environments. Here, we report low temperature (80 °C) anoxic hydrothermal experiments using starting assemblages similar to the constituents of the matrices of the most pristine CM chondrite and S‐rich and S‐free fluids. Cronstedtite crystals formed only in S‐free experiments under circumneutral conditions with the highest Fe/Si ratios. Fe‐rich tochilinite with chemical and structural characteristics similar to chondritic tochilinite was observed in S‐bearing experiments. We observed a positive correlation between the Mg content in the hydroxide layer of synthetic tochilinite and temperature, suggesting that the composition of tochilinite is a proxy for the alteration temperature in CM chondrites. Using this relation, we estimate the mean precipitation temperatures of tochilinite to be 120–160 °C for CM chondrites. Given the different temperature ranges of tochilinite and cronstedtite in our experiments, we propose that Fe‐rich tochilinite crystals resulted from the alteration of metal beads under S‐bearing alkaline conditions at T = 120–160 °C followed by cronstedtite crystals formed by the reaction of matrix amorphous silicates, metal beads, and water at a low temperature (50–120 °C).  相似文献   

14.
Abstract— CM2 carbonaceous chondrites are the most primitive material present in the solar system, and some of their subtypes, the CM and CI chondrites, contain up to 2 wt% of organic carbon. The CM2 carbonaceous chondrites contain a wide variety of complex amino acids, while the CI1 meteorites Orgueil and Ivuna display a much simpler composition, with only glycine and β‐alanine present in significant abundances. CM1 carbonaceous chondrites show a higher degree of aqueous alteration than CM2 types and therefore provide an important link between the CM2 and CI1 carbonaceous chondrites. Relative amino acid concentrations have been shown to be indicative for parent body processes with respect to the formation of this class of compounds. In order to understand the relationship of the amino acid composition between these three types of meteorites, we have analyzed for the first time three Antarctic CM1 chondrites, Meteorite Hills (MET) 01070, Allan Hills (ALH) 88045, and LaPaz Icefield (LAP) 02277, using gas chromatography‐mass spectrometry (GC‐MS) and high performance liquid chromatography‐fluorescence detection (HPLC‐FD). The concentrations of the eight most abundant amino acids in these meteorites were compared to those of the CM2s Murchison, Murray, Mighei, Lewis Cliff (LEW) 90500, ALH 83100, as well as the CI1s Orgueil and Ivuna. The total amino acid concentration in CM1 carbonaceous chondrites was found to be much lower than the average of the CM2s. Relative amino acid abundances were compared in order to identify synthetic relationships between the amino acid compositions in these meteorite classes. Our data support the hypothesis that amino acids in CM‐ and CI‐type meteorites were synthesized under different physical and chemical conditions and may best be explained with differences in the abundances of precursor compounds in the source regions of their parent bodies in combination with the decomposition of amino acids during extended aqueous alteration.  相似文献   

15.
Abstract— We used high‐resolution transmission electron microscopy (HRTEM), electron tomography, electron energy‐loss spectroscopy (EELS), and energy‐dispersive spectroscopy (EDS) to investigate the structure and composition of polyhedral serpentine grains that occur in the matrices and fine‐grained rims of the Murchison, Mighei, and Cold Bokkeveld CM chondrites. The structure of these grains is similar to terrestrial polygonal serpentine, but the data show that some have spherical or subspherical, rather than cylindrical morphologies. We therefore propose that the term polyhedral rather than polygonal be used to describe this material. EDS shows that the polyhedral grains are rich in Mg with up to 8 atom% Fe. EELS indicates that 70% of the Fe occurs as Fe3+. Alteration of cronstedtite on the meteorite parent body under relatively oxidizing conditions is one probable pathway by which the polyhedral material formed. The polyhedral grains are the end‐member serpentine in a mineralogic alteration sequence for the CM chondrites.  相似文献   

16.
Abstract— The fall and recovery of the Tagish Lake meteorite in British Columbia in January 2000 provided a unique opportunity to study relatively pristine samples of carbonaceous chondrite material. Measurements of the oxygen isotopic composition of water extracted under stepped pyrolysis from a bulk sample of this meteorite have allowed us to make comparisons with similar data obtained from CI and CM chondrites and so further investigate any relationships that may exist between these meteorites. The much lower yield of water bearing a terrestrial signature in Tagish Lake is indicative of the pristine nature of the meteorite. The relationship between the isotopic composition of this water and reported isotopic values for carbonates, bulk matrix and whole rock have been used to infer the extent and conditions under which parent‐body aqueous alteration occurred. In Tagish Lake the difference in Δ17O isotopic composition between the water and other phases is greater than that found in either CM or CI chondrites suggesting that reaction and isotopic exchange between components was more limited. This in turn suggests that in the case of Tagish Lake conditions during the processes of aqueous alteration on the parent body, which ultimately controlled the formation of new minerals, were distinct from those on both CI and CM parent bodies.  相似文献   

17.
Abstract— Thermochemical equilibria are calculated in the multicomponent gas‐solution‐rock system in order to evaluate the formation conditions of fayalite, (Fe0.88–1.0Mg0.12–0)2SiO4, Fa88–100, in unequilibrated chondrites. Effects of temperature, pressure, water/rock ratio, rock composition, and progress of alteration are evaluated. The modeling shows that fayalite can form as a minor secondary and transient phase with and without aqueous solution. Fayalite can form at temperatures below ?350 °C, but only in a narrow range of water/rock ratios that designates a transition between aqueous and metamorphic conditions. Pure fayalite forms at lower temperatures, higher water/rock ratios, and elevated pressures that correspond to higher H2/H2O ratios. Lower pressure and water/rock ratios and higher temperatures favor higher Mg content in olivine. In equilibrium assemblages, fayalite usually coexists with troilite, kamacite, magnetite, chromite, Ca‐Fe pyroxene, and phyllosilicates. Formation of fayalite can be driven by changes in temperature, pressure, H2/H2O, and water/rock ratios. However, in fayalite‐bearing ordinary and CV3 carbonaceous chondrites, the mineral could have formed during the aqueous‐to‐metamorphic transition. Dissolution of amorphous silicates in matrices and/or silica grains, as well as low activities of Mg solutes, favored aqueous precipitation of fayalite. During subsequent metamorphism, fayalite could have formed through the reduction of magnetite and/or dehydration of ferrous serpentine. Further metamorphism should have caused reductive transformation of fayalite to Ca‐Fe pyroxene and secondary metal, which is consistent with observations in metamorphosed chondrites. Although bulk compositions of matrices/chondrites have only a minor effect on fayalite stability, specific alteration paths led to different occurrences, quantities, and compositions of fayalite in chondrites.  相似文献   

18.
Abstract— Ar‐rich noble gases, the so‐called “subsolar” noble gases, are a major component of heavy primordial noble gases in unequilibrated ordinary chondrites and some classes of anhydrous carbonaceous chondrites, whereas they are almost absent in hydrous carbonaceous chondrites that suffered extensive aqueous alteration. To understand the effects of aqueous alteration on the abundance of Ar‐rich noble gases, we performed an aqueous alteration experiments on the Ningqiang type 3 carbonaceous chondrite that consists entirely of anhydrous minerals and contains Ar‐rich noble gases. Powdered samples and deionized neutral water were kept at 200 °C for 10 and 20 days, respectively. Mineralogical analyses show that, during the 10‐day alteration, serpentine and hematite formed at the expense of olivine, low‐Ca pyroxene, and sulfide. Noble gas analyses show that the 10‐day alteration of natural Ningqiang removed 79% of the primordial 36Ar, 68% of the 84Kr, and 60% of the 132Xe, but only 45% of the 4He and 53% of the primordial 20Ne. Calculated elemental ratios of the noble gases removed during the 10‐day alteration are in the range of those of Ar‐rich noble gases. These results indicate that Ar‐rich noble gases are located in materials that are very susceptible to aqueous alteration. In contrast, heavy primordial noble gases remaining in the altered samples are close to Q gas in elemental and isotope compositions. This indicates that phase Q is much more resistant to aqueous alteration than the host phases of Ar‐rich noble gases. In the 20‐day sample, the mineralogical and noble gas signatures are basically similar to those of the 10‐day sample, indicating that the loss of Ar‐rich noble gases was completed within the 10‐day alteration. Our results suggest that almost all of the Ar‐rich noble gases were lost from primitive asteroids during early, low‐temperature aqueous alteration.  相似文献   

19.
Abstract— Mid‐infrared absorption spectra for all types of carbonaceous chondrites were obtained in this study to establish a versatile method for spectroscopic classification of carbonaceous chondrites. Infrared spectra were measured using a conventional KBr pellet method and diamond press method. Spectra of hydrous carbonaceous chondrites exhibit intense O‐H stretching vibrations. CI chondrites are identifiable by a characteristic sharp absorption band appearing at 3685 cm?1, which is mainly attributable to serpentine. X‐ray diffraction analysis showed the presence of serpentine. However, Yamato (Y‐) 82162 (C1) does not have the band at 3685 cm?1 because of its thermal metamorphism. CM and CR chondrites have an intense absorption band at approximately 3600 cm?1. This absorption tends to appear in CM chondrites more strongly than CR chondrites because the intensity ratios of an OH stretching mode at 3520 cm?1 compared to 3400 cm?1 for CM chondrites are in the range of 0.95–1.04, which is systematically higher than those of CR chondrites (0.86–0.88). Therefore, the two types of chondrites are distinguishable by their respective infrared spectra. The spectrum feature of the Tagish Lake meteorite is attributable to neither CI nor CM chondrites. CO chondrites are characterized by weak and broad absorption at 3400 cm?1. CV chondrites have weak or negligible absorption of water. CK chondrites also have no water‐induced absorption. CH and CB chondrites have a sharp absorption at 3692 cm?1 indicating the presence of chrysotile, which is also supported by observations of X‐ray diffraction and TEM. The combination of spectroscopic classification and the diamond press method allows classification of carbonaceous chondrites of very valuable samples with small quantities. As one example, carbonaceous chondrite clasts in brecciated meteorites were classified using our technique. Infrared spectra for a fragment of carbonaceous clasts (<1 μg) separated from Willard (b) and Tsukuba were measured. The 3685 cm?1 band found in CI chondrites was clearly detected in the clasts, indicating that they are CI‐like clasts.  相似文献   

20.
Meteorite Hills (MET) 01075 is unique among the CM carbonaceous chondrites in containing the feldspathoid mineral sodalite, and hence it may provide valuable evidence for a nebular or parent body process that has not been previously recorded by this meteorite group. MET 01075 is composed of aqueously altered chondrules and calcium‐ and aluminum‐rich inclusions (CAIs) in a matrix that is predominantly made of serpentine‐ and tochilinite‐rich particles. The chondrules have been impact flattened and define a foliation petrofabric. Sodalite occurs in a 0.6 mm size CAI that also contains spinel, perovskite, and diopside together with Fe‐rich phyllosilicate and calcite. By analogy with feldspathoid‐bearing CAIs in the CV and CO carbonaceous chondrites, the sodalite is interpreted to have formed by replacement of melilite or anorthite during alkali‐halogen metasomatism in a parent body environment. While it is possible that the CAI was metasomatized in a precursor parent body, then excavated and incorporated into the MET 01075 parent body, in situ metasomatism is the favored model. The brief episode of relatively high temperature water–rock interaction was driven by radiogenic or impact heating, and most of the evidence for metasomatism was erased by subsequent lower temperature aqueous alteration. MET 01075 is very unusual in sampling a CM parent body region that underwent early alkali‐halogen metasomatism and has retained one of its products.  相似文献   

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