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1.
Transmission electron microscope studies of fine‐grained rims in three CM2 carbonaceous chondrites, Y‐791198, Murchison, and ALH 81002, have revealed the presence of widespread nanoparticles with a distinctive core–shell structure, invariably associated with carbonaceous material. These nanoparticles vary in size from ~20 nm up to 50 nm in diameter and consist of a core of Fe,Ni carbide surrounded by a continuous layer of polycrystalline magnetite. These magnetite shells are 5–7 nm in thickness irrespective of the diameter of the core Fe,Ni carbide grains. A narrow layer of amorphous carbon a few nanometers in thickness is present separating the carbide core from the magnetite shell in all the nanoparticles observed. The Fe,Ni carbide phases that constitute the core are consistent with both haxonite and cohenite, based on electron diffraction data, energy dispersive X‐ray analysis, and electron energy loss spectroscopy. Z‐contrast scanning transmission electron microscopy shows that these core–shell magnetite‐carbide nanoparticles can occur as individual isolated grains, but more commonly occur in clusters of multiple particles. In addition, energy‐filtered transmission electron microscopy (EFTEM) images show that in all cases, the nanoparticles are embedded within regions of carbonaceous material or are coated with carbonaceous material. The observed nanostructures of the carbides and their association with carbonaceous material can be interpreted as being indicative of Fischer–Tropsch‐type (FTT) reactions catalyzed by nanophase Fe,Ni metal grains that were carburized during the catalysis reaction. The most likely environment for these FTT reactions appears to be the solar nebula consistent with the high thermal stability of haxonite and cohenite, compared with other carbides and the evidence of localized catalytic graphitization of the carbonaceous material. However, the possibility that such reactions occurred within the CM parent body cannot be excluded, although this scenario seems unlikely, because the kinetics of the reaction would be extremely slow at the temperatures inferred for CM asteroidal parent bodies. In addition, carbides are unlikely to be stable under the oxidizing conditions of alteration experienced by CM chondrites. Instead, it is most probable that the magnetite rims on all the carbide particles are the product of parent body oxidation of Fe,Ni carbides, but this oxidation was incomplete, because of the buildup of an impermeable layer of amorphous carbon at the interface between the magnetite and the carbide phase that arrested the reaction before it went to completion. These observations suggest that although FTT catalysis reactions may not have been the major mechanism of organic material formation within the solar nebula, they nevertheless contributed to the inventory of complex insoluble organic matter that is present in carbonaceous chondrites.  相似文献   

2.
The Kamiomi, Sashima-gun (Iwai-shi), Ibaraki-ken, Japan, chondrite (observed to fall in spring, during the period 1913–6), consists of olivine, orthopyroxene, nickel-iron and troilite with minor amount of plagioclase, clinopyroxene, apatite and chromite. The average molar composition of olivine (Fa19) and orthopyroxene (Fs17) indicates that Kamiomi is a typical olivine bronzite chondrite. From the well-recrystallized texture, the presence of poorly-definable chondrules, homogeneous composition of olivine and absence of glass, this chondrite could be classified in petrologic type 5. The bulk chemical composition, especially, total Fe (27.33%) and metallic Fe (17.00%) as well as Fetotal/SiO2(0.72), Femetal/Fetotal (0–633) and SiO2/MgO (1.59) support the above conclusion. Coexistence of heavily-shocked olivine grains in the matrix composed of olivines and pyroxenes which suffered from light to moderate shock effect suggest that impacting phenomena, small-scaled but locally strong, occurred on the Kamiomi parent body.  相似文献   

3.
Abstract— We report the results of our petrological and mineralogical study of Fe‐Ni metal in type 3 ordinary and CO chondrites, and the ungrouped carbonaceous chondrite Acfer 094. Fe‐Ni metal in ordinary and CO chondrites occurs in chondrule interiors, on chondrule surfaces, and as isolated grains in the matrix. Isolated Ni‐rich metal in chondrites of petrologic type lower than type 3.10 is enriched in Co relative to the kamacite in chondrules. However, Ni‐rich metal in type 3.15–3.9 chondrites always contains less Co than does kamacite. Fe‐Ni metal grains in chondrules in Semarkona typically show plessitic intergrowths consisting of submicrometer kamacite and Ni‐rich regions. Metal in other type 3 chondrites is composed of fine‐ to coarse‐grained aggregates of kamacite and Ni‐rich metal, resulting from metamorphism in the parent body. We found that the number density of Ni‐rich grains in metal (number of Ni‐rich grains per unit area of metal) in chondrules systematically decreases with increasing petrologic type. Thus, Fe‐Ni metal is a highly sensitive recorder of metamorphism in ordinary and carbonaceous chondrites, and can be used to distinguish petrologic type and identify the least thermally metamorphosed chondrites. Among the known ordinary and CO chondrites, Semarkona is the most primitive. The range of metamorphic temperatures were similar for type 3 ordinary and CO chondrites, despite them having different parent bodies. Most Fe‐Ni metal in Acfer 094 is martensite, and it preserves primary features. The degree of metamorphism is lower in Acfer 094, a true type 3.00 chondrite, than in Semarkona, which should be reclassified as type 3.01.  相似文献   

4.
We have investigated the fine‐grained matrix of the least‐altered unequilibrated ordinary chondrite (UOC) Semarkona (LL3.00) using different electron microscope techniques. Unlike previous studies, which found that the matrix of Semarkona was extensively altered to phyllosilicates, we have discovered the widespread occurrence of much more pristine amorphous silicates in the sample that we have studied. Detailed TEM study shows that these materials occur pervasively in the matrix as (1) continuous groundmass; (2) distinct, circular to subrounded features, which contain nanometric‐size sulfides and carbides; or (3) distinct objects containing parallel, linear features composed of sulfides and voids. These amorphous silicates have many textural and compositional similarities to the occurrences of amorphous silicates found in pristine carbonaceous chondrites (CCs); however, minor differences were also identified. Most of the textural and chemical differences suggest that these materials formed at different times and locations in the solar nebula, compared to matrix materials in CCs. Nevertheless, their occurrence suggests that the amorphous silicates in Semarkona formed by similar processes to those proposed for amorphous silicates in CCs, that is, rapid cooling that favored disequilibrium condensation of material evaporated during chondrule‐forming events. In addition, the occurrence of minimally altered amorphous silicates in Semarkona demonstrates that the effects of aqueous alteration, which have been widely described in this meteorite, are not pervasive. Instead, our new observations demonstrate that aqueous alteration has affected Semarkona heterogeneously and that locally, regions of much more pristine matrix that have escaped extensive alteration are still preserved within this meteorite. Such materials provide significant new insights into the pristine characteristics of ordinary chondrite matrix material that has not been previously available.  相似文献   

5.
The mineralogical and chemical compositions of meteorites from the Motta di Conti, Vercelli, Italy, shower (February 29, 1868) have been determined. Microprobe analyses, of olivine (Fa19,6) and orthopyroxene (Fs17,8), as well as the bulk chemical composition, particularly the ratios of SiO2/MgO (1.50), Fe°/Ni° (11.03), Fetotal/SiO2 (0.81), Fe°/Fetotal (0.70) and the content of Fetotal (28.60%) classify the meteorite as an H-group chondrite. The percentage of total metallic nickel-iron (22.06%) is somewhat higher than the average in H-group chondrites. The texture of our stone shows evidence of metamorphism. The integration between matrix and chondrules is advanced and may suggest a high petrographic grade, but the identification of several microscopic features (e.g. small grains of monoclinic twinned pyroxene, FeNi-FeS intergrowths, globules and mosaic) leads to the conclusion that a variety of petrographic types (4–6) are present. Metamorphic equilibration in chondrites is discussed and a preliminary hypothesis for H4–6 chondrites is suggested.  相似文献   

6.
Compositional and structural analyses of CI chondrite iron–nickel sulfide grains reveal heterogeneity both across and within the Orgueil and Alais meteorites. Orgueil grains with the 4C monoclinic pyrrhotite structure have variable metal‐to‐sulfur ratios and nickel contents. These range from the nominal ratio of 0.875 for Fe7S8 with <1 atom% nickel to a high metal‐to‐sulfur ratio of 0.97 with 15 atom% nickel. These data reveal a previously unrecognized low‐temperature solid solution between Fe7S8 and Fe5Ni3S8. We have also identified 6C monoclinic pyrrhotite among the Orgueil iron–nickel sulfides. The occurrence of pentlandite in Orgueil is confirmed for the first time crystallographically. In contrast, sulfide grains in Alais do not show the same spread in composition and structure; rather they represent the endmembers: low‐Ni 4C monoclinic pyrrhotite and pentlandite. We investigate possible formation/alteration scenarios: crystallization from a melt, solid‐state diffusion and/or exsolution, oxidation of pre‐existing sulfides, and precipitation from a fluid. Sulfide grains are sensitive to alteration conditions; these data suggest that the structures and compositions of the sulfide assemblages in Orgueil and Alais were established by late‐stage parent body aqueous alteration, followed in some cases by low‐temperature solid‐state processes. The samples record different alteration histories, with Orgueil experiencing lower equilibration temperatures (25 °C) than Alais (100–135 °C). We conclude that millimeter‐scale heterogeneity existed in alteration conditions (e.g., temperature, pH, oxygen fugacity, sulfur fugacity, duration of alteration) on the parent body. This variability is evidenced by the diversity among sulfide grains located within millimeters of one another.  相似文献   

7.
TAM5.29 is an extraterrestrial dust grain, collected on the Transantarctic Mountains (TAM). Its mineralogy is dominated by an Fe‐rich matrix composed of platy fayalitic olivines and clasts of andradite surrounded by diopside‐jarosite mantles; chondrules are absent. TAM5.29 records a complex geological history with evidence of extensive thermal metamorphism in the presence of fluids at T < 300 °C. Alteration was terminated by an impact, resulting in shock melt veins and compaction‐orientated foliation of olivine. A second episode of alteration at lower temperatures (<100 °C) occurred postimpact and is either parent body or terrestrial in origin and resulted in the formation of iddingsite. The lack of chondrules is explained by random subsampling of the parent body, with TAM5.29 representing a matrix‐only fragment. On the basis of bulk chemical composition, mineralogy, and geological history TAM5.29 demonstrates affinities to the CVox group with a mineralogical assemblage in between the Allende‐like and Bali‐like subgroups (CVoxA and TAM5.29 are rich in andradite, magnetite, and FeNiS, but CVoxA lacks hydrated minerals, common in TAM5.29; conversely, CVoxB are rich in hydrated phyllosilicates but contain almost pure fayalite, not found in TAM5.29). In addition, TAM5.29 has a slightly different metasomatic history, in between the oxidized and reduced CV metamorphic grades while also recording higher oxidizing conditions as compared to the known CV chondrites. This study represents the third CV‐like cosmic dust particle, containing a unique composition, mineralogy, and fabric, demonstrating variation in the thermal metamorphic history of the CV parent body(‐ies).  相似文献   

8.
Abstract— The thermal metamorphism grade of organic matter (OM) trapped in 6 unequilibrated ordinary chondrites (UOCs) (Semarkona [LL 3.0], Bishunpur [L/LL 3.1], Krymka [LL 3.1], Chainpur [LL 3.4], Inman [L/LL 3.4], and Tieschitz [H/L 3.6]) has been investigated with Raman spectroscopy in the region of the first‐order carbon bands. The carbonaceous chondrite Renazzo (CR2) was also investigated and used as a reference object for comparison, owing to the fact that previous studies pointed to the OM in this meteorite as being the most pristine among all chondrites. The results show that the OM thermal metamorphic grade: 1) follows the hierarchy Renazzo << Semarkona << other UOCs; 2) is well correlated to the petrographic type of the studied objects; and 3) is also well correlated with the isotopic enrichment δ15N. These results are strikingly consistent with earlier cosmochemical studies, in particular, the scenario proposed by Alexander et al. (1998). Thermal metamorphism in the parent body appears as the main evolution process of OM in UOCs, demonstrating that nebular heating was extremely weak and that OM burial results in the destabilization of an initial isotopic composition with high δD and δ15N. Furthermore, the clear discrimination between Renazzo, Semarkona, and other UOCs shows: 1) Semarkona is a very peculiar UOC—by far the most pristine; and 2) Raman spectroscopy is a valid and valuable tool for deriving petrographic sub‐types (especially the low ones) that should be used in the future to complement current techniques. We compare our results with other current techniques, namely, induced thermo‐luminescence and opaques petrography. Other results have been obtained. First, humic coals are not strictly valid standard materials for meteoritic OM but are helpful in the study of evolutionary trends due to thermal metamorphism. Second, terrestrial weathering has a huge effect on OM structure, particularly in Inman, which is a find. Finally, the earlier statement that fine‐grained chondrule rims and matrix in Semarkona could be the source of smectite‐rich IDPs is not valid, given the different degree of structural order of their OM.  相似文献   

9.
Abstract The matrix of Vigarano, a meteorite which belongs to the reduced subgroup of the CV3 chondrites, contains small amounts (<10%) of ferrihydrite and smectite. These hydrous minerals occur together as fine fibrous intergrowths between anhydrous silicate and oxide grains. Coarser crystals of ferrihydrite fill fractures that cut matrix minerals, and smectite also lines narrow channels within olivine grains. These channels may have formed by preferential alteration of olivines along (100)-parallel defects. Formation of ferrihydrite and smectite in the matrix of Vigarano was the result of mild aqueous alteration in a low-temperature (<150 °C), oxidising parent body environment. Partial equilibration of matrix olivines indicates that alteration was followed by thermal metamorphism with a peak temperature of 400–500 °C. Mineralogically similar alteration products, which also were formed by parent body processes, have previously been described from the matrices of four CV meteorites: Bali, Grosnaja, Kaba and Mokoia, all of which belong to the oxidised subgroup. This discovery of the products of oxidative aqueous alteration in Vigarano has important consequences for understanding the chemical and thermal history of the CV class of meteorites.  相似文献   

10.
Abstract— Calculations of the formation of seven types of chondrules in Semarkona from a gas of solar composition were performed with the FACT computer program to predict the chemistries of oxides (including silicates), developed by the authors and their colleagues. The constrained equilibrium theory was used in the calculations with two nucleation constraints suggested by nucleation theory. The first constraint was the blocking of Fe and other metal gaseous atoms from condensing to form solids or liquids because of very high surface free energies and high surface tensions of the solid and liquid metals, respectively. The second constraint was the blocking of the condensation of solids and the formation of metastable liquid oxides (including silicates) well below their liquidus temperatures. Our laboratory experiments suggested subcooling of type IIA chondrule compositions of 400 degrees or more below the liquidus temperature. The blocking of iron leads to a supersaturation of Fe atoms, so that the partial pressure of Fe (pFe) is larger than the partial pressure at equilibrium (pFe(eq)). The supersaturation ratio S = pFe/pFe(eq) becomes larger than 1 and increases rapidly with a decrease in temperature. This drives the reaction Fe + H2O ? H2 + FeO to the right. With S = 100, the activity of FeO in the liquid droplet is 100 times as large as the value at equilibrium. The FeO activities are a function of temperature and provide relative average temperatures of the crystallization of chondrules. Our calculations for the LL3.0 chondrite Semarkona and our study of some non‐equilibrium effects lead to accurate representations of the compositions of chondrules of types IA, IAB, IB, IIA, IIAB, IIB, and CC. Our concepts readily explain both the variety of FeO concentrations in the different chondrule types and the entire process of chondrule formation. Our theory is unified and could possibly explain the formation of chondrules in all chondritic meteorites as well as provide a simple explanation for the complex chemistries of chondrites, and especially for type 3 chondrites.  相似文献   

11.
Dmisteinbergite, a hexagonal form of CaAl2Si2O8, was found in a compact type A Ca-Al-rich inclusion (CAI) in the Allende CV3 chondrite. Scanning and transmission electron microscopic observations show that dmisteinbergite was always in contact with grossular and grossular was in contact with melilite. In addition, there is a crystallographic relationship between dmisteinbergite and anorthite. Based on the textural and crystallographic evidence, the following mineralogical alteration processes are proposed to have occurred in the CAI. (1) Melilite was replaced by grossular. High densities of vesicles in the grossular indicate that hydrogrossular might have been the primary alteration phase and dehydrated by later metamorphism. (2) Dmisteinbergite formed from (hydro)grossular through a reaction with Si-rich fluid. (3) Nano-sized minerals are formed within dmisteinbergite. (4) Dmisteinbergite was transformed to anorthite. (5) Both anorthite and dmisteinbergite were altered to nepheline. (6) Hydrogrossular was dehydrated to grossular. (Hydro)grossular, dmisteinbergite, anorthite, and nepheline in the CAI seem to have formed in the course of metasomatism that occurred in the Allende parent body. Except for the hydrogrossular dehydration, these reactions could have occurred at moderate temperature (200–250°C) in high pH fluids (pH 13–14) according to past experimental studies. Episodic changes in fluid composition seem to have occurred before reactions (2), (4), and (5), because these reactions were not completed before the next reaction started. Higher temperature is required for reactions (5) and (6) to occur. Our observation of the CAI suggests that it experienced multiple episodes of metasomatism as temperatures were rising in the Allende parent asteroid.  相似文献   

12.
The crystal structures of orthopyroxene (En86.3Fs8.6Wo5.1, space group Pbca) and pigeonite (En81.7Fs8.8Wo9.5, space group P21/c) from the Almahata Sitta ureilite (fragment#051) have been refined to R1 indices of 3.10% and 2.53%, respectively, using single-crystal X-ray diffraction data. The unit formulas were calculated from electron microprobe analysis, and the occupancies at the M1 and M2 sites were refined for both pyroxenes from the single-crystal diffraction data. The results indicate a rather disordered intracrystalline Fe2+-Mg cation distribution over the M1 and M2 sites, with a closure temperature of 726(±55)°C for orthopyroxene and 704(±110)°C for pigeonite, suggesting fast cooling of these pyroxenes. The Mössbauer spectrum of the Fe-Ni metal particles of Almahata Sitta ureilite (fragment#051) is dominated by two overlapping magnetic sextets that are assigned to Fe atoms in Si-bearing kamacite, and arise from two different nearest-neighbor configurations of Fe* (=Fe+Ni) and Si atoms in the bcc structure of kamacite; (8F*, 0Si) and (7Fe*, 1Si). In addition, the spectrum shows weak absorption peaks that are attributed to the presence of small amounts of cohenite [(Fe,Ni)3C], schreibersite [(Fe,Ni)3P], and an Fe-oxide/hydroxide phase. The fast cooling of pyroxene to the closure temperature (after equilibration at ~1200°C) and the incorporation of Si in kamacite can be interpreted as due to a shock event that took place on the meteorite parent body, consistent with the proposed formation history of ureilites parent body where a fast cooling has occurred at a later stage of its formation.  相似文献   

13.
Abstract— We report measurements of K isotope ratios in 28 Semarkona chondrules with a wide range of petrologic types and bulk compositions as well as the compositions of CPX‐mesostasis pairs in 17 type I Semarkona chondrules, including two chondrules with radial alkali zonation and 19 type II chondrules. Despite the wide range in K/Al ratios, no systematic variations in K isotopic compositions were found. Semarkona chondrules do not record a simple history of Rayleigh‐type loss of K. Experimentally determined evaporation rates suggest that considerable alkali evaporation would have occurred during chondrule formation. Nevertheless, based on Na CPX‐mesostasis distribution coefficients, the alkali contents of the cores of most chondrules in Semarkona were probably established at the time of final crystallization. However, Na CPX‐mesostasis distribution coefficients also show that alkali zonation in type I Semarkona chondrules was produced by entry of alkalis after solidification, probably during parent body alteration. This alkali metasomatism may have gone to completion in some chondrules. Our preferred explanation for the lack of systematic isotopic enrichments, even in alkali depleted type I chondrule cores, is that they exchanged with the ambient gas as they cooled.  相似文献   

14.
Northwest Africa (NWA) 5232, an 18.5 kg polymict eucrite, comprises eucritic and exogenic CM carbonaceous chondrite clasts within a clastic matrix. Basaltic clasts are the most abundant eucritic clast type and show a range of textures and grain size, from subophitic to granoblastic. Other eucritic clast types present include cumulate (high‐En pyroxene), pyroxene‐lath, olivine rich with symplectite intergrowths as a break‐down product of a quickly cooled Fe‐rich metastable pyroxferroite, and breccia (fragments of a previously consolidated breccia) clasts. A variable cooling rate and degree of thermal metamorphism, followed by a complex brecciation history, can be inferred for the clasts based on clast rounding, crystallization (and recrystallization) textures, pyroxene major and minor element compositions, and pyroxene exsolution. The range in δ18O of clasts and matrix of NWA 5232 reflects its origin as a breccia of mixed clasts dominated by eucritic lithologies. The oxygen isotopic compositions of the carbonaceous chondrite clasts identify them as belonging to CM group and indicate that these clasts experienced a low degree of aqueous alteration while part of their parent body. The complex evolutionary history of NWA 5232 implies that large‐scale impact excavation and mixing was an active process on the surface of the HED parent body, likely 4 Vesta.  相似文献   

15.
The Kyle, Texas, U.S.A., chondrite was identified in 1965. Electron microprobe analyses and microscopic examination show the following mineralogy: olivine (Fa 26.2 mole %), orthopyroxene (Fs 21.0 mole %), clinopyroxene, plagioclase (An 10.3 mole %), chlorapatite, whitlockite, kamacite, taenite, troilite, chromite, and an iron-bearing terrestrial weathering product. Eutectic intergrowths of metaltroilite and a brecciated matrix indicate that the Kyle chondrite was shocked. Recrystallization and shock have obliterated chondrule-matrix boundaries. A chemical analysis of the meteorite shows the following results (in weight %): Fe 0.38, Ni 1.22, Co 0.05, FeS 5.98, SiO2 38.41, TiO2 0.11, Al2O3 2.13, Cr2O3 0.55, Fe2O3 8.02, FeO 14.83, MnO 0.31, MgO 23.10, CaO 1.60, Na2O 0.74, K2O 0.08, P2O5 0.19, H2O+ 1.73, H2O? 0.37, C 0.03, Sum 99.83. On the basis of bulk chemistry, composition of olivine and orthopyroxene, and the recrystallized matrix, the Kyle meteorite is classified as an L6 chondrite.  相似文献   

16.
Abstract— The Carcote meteorite, detected in 1888 in the northern Chilean Andes, is a brecciated, weakly shocked H5 chondrite. It contains a few barred olivine chondrules and, even more rarely, fan-shaped or granular orthopyroxene chondrules. The chondrules are situated in a fine-grained matrix that consists predominantly of olivine and orthopyroxene with accessory clinopyroxene, troilite, chromite, merrillite, and plagioclase. The metal phase is mainly kamacite with subordinate taenite and traces of native Cu. In its bulk rock composition, Carcote compares well with other H5 chondrites so far analysed, except for a distinctly higher C content. Microprobe analyses revealed the following mineral compositions: olivine (Fa16.5–20), orthopyroxene (Fs14–17.5), diopsidic clinopyroxene (FS6–7), plagioclase (An15–20). Troilite is stoichimetric FeS with traces of Ni and Cr; chromite has Cr/(Cr + Al) of 0.86, Fe2+/(Fe2+ + Mg) of 0.80-0.88 and contains considerable amounts of Ti, Mn, and Zn. Merrillite is close to the theoretical formula Ca18(Mg, Fe)2Na2(PO4)14, although with a Na deficiency not compensated for by excess Ca; the Mg/(Mg + Fe2+) ratio of the Carcote merrilite is 0.93-0.95. Kamacite and taenite have Ni contents of 5.6–7.2 and 17.1–23.4 wt%, respectively. Native Cu contains about 3.1–3.3 wt% Fe and 1.6 wt% Ni. Application of different geothermometers to the Carcote H5 chondrite yielded apparently inconsistent results. The highest temperature range of 850–950 °C (at 1 bar) is derived from the Ca-in-opx thermometer. From the cpx-opx solvus geothermometers and the two-pyroxene Fe-Mg exchange geothermometer, a lower temperature range of 750–840 °C is estimated, whereas lower and more variable temperatures of 630–770 °C are obtained from the Ca-in-olivine geothermometer. Recent calibrations of the olivine-spinel geothermometer yielded a still lower temperature range of 570–670 °C, which fits well to the temperature information derived from the Ni distribution between kamacite and taenite. Judging from crystal chemical considerations, we assume that these different temperatures reflect the closure of different exchange equilibria during cooling of the meteorite parent body.  相似文献   

17.
Abstract— Cooling rates of chondrules provide important constraints on the formation process of chondrite components at high temperatures. Although many dynamic crystallization experiments have been performed to obtain the cooling rate of chondrules, these only provide a possible range of cooling rates, rather than providing actual measured values from natural chondrules. We have developed a new model to calculate chondrule cooling rates by using the Fe‐Mg chemical zoning profile of olivine, considering diffusional modification of zoning profiles as crystals grow by fractional crystallization from a chondrule melt. The model was successfully verified by reproducing the Fe‐Mg zoning profiles obtained in dynamic crystallization experiments on analogs for type II chondrules in Semarkona. We applied the model to calculating cooling rates for olivine grains of type II porphyritic olivine chondrules in the Semarkona (LL3.00) ordinary chondrite. Calculated cooling rates show a wide range from 0.7 °C/h to 2400 °C/h and are broadly consistent with those obtained by dynamic crystallization experiments (10–1000 °C/h). Variations in cooling rates in individual chondrules can be attributed to the fact that we modeled grains with different core Fa compositions that are more Fe‐rich either because of sectioning effects or because of delayed nucleation. Variations in cooling rates among chondrules suggest that each chondrule formed in different conditions, for example in regions with varying gas density, and assembled in the Semarkona parent body after chondrule formation.  相似文献   

18.
Abstract— The iron-magnesium exchange between M1 and M2 sites in orthopyroxene is a reversible reaction that records the latest event in the thermal evolution of the host rock. A kinetic analysis of this process has been applied to 16 orthopyroxene single crystals from 7 different diogenites to constrain the cooling history of their parent body. The Fe2+-Mg ordering degrees have been determined by single-crystal x-ray diffraction. The Fe2+-Mg ordering closure temperatures were very homogeneous within each sample and ranged, for all diogenites studied, between 311 ± 29 °C and 408 ± 10 °C. Cooling rates at these closure temperatures were calculated using a numerical method developed by Ganguly (1982). These ranged between ～5 °C/104 year in Johnstown and ～0.8 °C/year in Roda. A comparison with other achondrites studied with the same method showed that increasing closure temperatures correspond to increasing cooling rates and that meteorites from a same parent body exhibit similar closure temperature and cooling rate values. The cooling rates obtained for these diogenites, at their low closure temperatures, should probably be ascribed to a complex thermal history of their parent body, thus confirming Miyamoto and Takeda's theory (1994a) of excavation of deep crustal material due to impact events. The differences on cooling rate values for different diogenites could be due to different burial depths in the fragment ejected from the parent body.  相似文献   

19.
Abstract— We have measured the titanium isotopic compositions of 23 silicon carbide grains from the Orgueil (CI) carbonaceous chondrites for which isotopic compositions of silicon, carbon, and nitrogen and aluminum‐magnesium systematics had been measured previously. Using the 16 most‐precise measurements, we estimate the relative contributions of stellar nucleosynthesis during the asymptotic giant branch (AGB) phase and the initial compositions of the parent stars to the compositions of the grains. To do this, we compare our data to the results of several published stellar models that employ different values for some important parameters. Our analysis confirms that s‐process synthesis during the AGB phase only slightly modified the titanium compositions in the envelopes of the stars where mainstream silicon carbide grains formed, as it did for silicon. Our analysis suggests that the parent stars of the >1 μm silicon carbide grains that we measured were generally somewhat more massive than the Sun (2–3 M⊙) and had metallicities similar to or slightly higher than solar. Here we differ slightly from results of previous studies, which indicated masses at the lower end of the range 1.5–3 M⊙ and metallicities near solar. We also conclude that models using a standard 13C pocket, which produces a good match for the main component of s‐process elements in the solar system, overestimate the contribution of the 13C pocket to s‐process nucleosynthesis of titanium found in silicon carbide grains. Although previous studies have suggested that the solar system has a significantly different titanium isotopic composition than the parent stars of silicon carbide grains, we find no compelling evidence that the Sun falls off of the array defined by those stars. We also conclude that the Sun does lie on the low‐metallicity end of the silicon and titanium arrays defined by mainstream silicon carbide grains.  相似文献   

20.
We report the bulk C abundances, and C and O isotopic compositions of carbonates in 64 CM chondrites, 14 CR chondrites, 2 CI chondrites, LEW 85332 (C2), Kaba (CV3), and Semarkona (LL3.0). For the unheated CMs, the total ranges of carbonate isotopic compositions are δ13C ≈ 25–75‰ and δ18O ≈ 15–35‰, and bulk carbonate C contents range from 0.03 to 0.60 wt%. There is no simple correlation between carbonate abundance and isotopic composition, or between either of these parameters and the extent of alteration. Unless accretion was very heterogeneous, the uncorrelated variations in extent of alteration and carbonate abundance suggests that there was a period of open system behavior in the CM parent body, probably prior to or at the start of aqueous alteration. Most of the ranges in CM carbonate isotopic compositions can be explained by their formation at different temperatures (0–130 °C) from a single fluid in which the carbonate O isotopes were controlled by equilibrium with water (δ18O ≈ 5‰) and the C isotopes were controlled by equilibrium with CO and/or CH4 (δ13C ≈ ?33‰ or ?20‰ for CO‐ or CH4‐dominated systems, respectively). However, carbonate formation would have to have been inefficient, otherwise carbonate compositions would have resembled those of the starting fluid. A quite similar fluid composition (δ18O ≈ ?5.5‰, and δ13C ≈ ?31‰ or ?17‰ for CO‐ or CH4‐dominated systems, respectively) can explain the carbonate compositions of the CIs, although the formation temperatures would have been lower (~10–40 °C) and the relative abundances of calcite and dolomite may play a more important role in determining bulk carbonate compositions than in the CMs. The CR carbonates exhibit a similar range of O isotopes, but an almost bimodal distribution of C isotopes between more (δ13C ≈ 65–80‰) and less altered samples (δ13C ≈ 30–40‰). This bimodality can still be explained by precipitation from fluids with the same isotopic composition (δ18O ≈ ?9.25‰, and δ13C ≈ ?21‰ or ?8‰ for CO‐ or CH4‐dominated systems, respectively) if the less altered CRs had higher mole fractions of CO2 in their fluids. Semarkona and Kaba carbonates have some of the lightest C isotopic compositions of the meteorites studied here, probably because they formed at higher temperatures and/or from more CO2‐rich fluids. The fluids responsible for the alteration of chondrites and from which the carbonates formed were almost certainly accreted as ices. By analogy with cometary ices, CO2 and/or CO would have dominated the trapped volatile species in the ices. The chondrites studied are too oxidized for CO‐dominated fluids to have formed in their parent bodies. If CH4 was the dominant C species in the fluids during carbonate formation, it would have to have been generated in the parent bodies from CO and/or CO2 when oxidation of metal by water created high partial pressures of H2. The fact that the chondrite carbonate C/H2O mole ratios are of the order predicted for CO/CO2‐H2O ices that experienced temperatures of >50–100 K suggests that the chondrites formed at radial distances of <4–15 AU.  相似文献   

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