首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
Carbonaceous chondrites are classified into several groups. However, some are ungrouped. We studied one such ungrouped chondrite, Y‐82094, previously classified as a CO. In this chondrite, chondrules occupy 78 vol%, and the matrix is distinctly poor in abundance (11 vol%), compared with CO and other C chondrites. The average chondrule size is 0.33 mm, different from that in C chondrites. Although these features are similar to those in ordinary chondrites, Y‐82094 contains 3 vol% Ca‐Al‐rich inclusions and 5% amoeboid olivine aggregates (AOAs). Also, the bulk composition resembles that of CO chondrites, except for the volatile elements, which are highly depleted. The oxygen isotopic composition of Y‐82094 is within the range of CO and CV chondrites. Therefore, Y‐82094 is an ungrouped C chondrite, not similar to any other C chondrite previously reported. Thin FeO‐rich rims on AOA olivine and the mode of occurrence of Ni‐rich metal in the chondrules indicate that Y‐82094 is petrologic type 3.2. The extremely low abundance of type II chondrules and high abundance of Fe‐Ni metal in the chondrules suggest reducing condition during chondrule formation. The depletion of volatile elements indicates that the components formed under high‐temperature conditions, and accreted to the parent body of Y‐82094. Our study suggests a wider range of formation conditions than currently recorded by the major C chondrite groups. Additionally, Y‐82094 may represent a new, previously unsampled, asteroidal body.  相似文献   

2.
Abstract– Chondrule compositions suggest either ferroan precursors and evaporation, or magnesian precursors and condensation. Type I chondrule precursors include granoblastic olivine aggregates (planetary or nebular) and fine‐grained (dustball) precursors. In carbonaceous chondrites, type I chondrule precursors were S‐free, while type II chondrules have higher Fe/Mn than in ordinary chondrites. Many type II chondrules contain diverse forsteritic relicts, consistent with polymict dustball precursors. The relationship between finer and coarser grained type I chondrules in ordinary chondrites suggests more evaporation from more highly melted chondrules. Fe metal in type I, and Na and S in type II chondrules indicate high partial pressures in ambient gas, as they are rapidly evaporated at canonical conditions. The occurrence of metal, sulfide, or low‐Ca pyroxene on chondrule rims suggests (re)condensation. In Semarkona type II chondrules, Na‐rich olivine cores, Na‐poor melt inclusions, and Na‐rich mesostases suggest evaporation followed by recondensation. Type II chondrules have correlated FeO and MnO, consistent with condensation onto forsteritic precursors, but with different ratios in carbonaceous chondrites and ordinary chondrites, indicating different redox history. The high partial pressures of lithophile elements require large dense clouds, either clumps in the protoplanetary disk, impact plumes, or bow shocks around protoplanets. In ordinary chondrites, clusters of type I and type II chondrules indicate high number densities and their similar oxygen isotopic compositions suggest recycling together. In carbonaceous chondrites, the much less abundant type II chondrules were probably added late to batches of type I chondrules from different O isotopic reservoirs.  相似文献   

3.
Abstract– We have examined Fe/Mn systematics of 34 type IIA chondrules in eight highly unequilibrated CO, CR, and ordinary chondrites using new data from this study and prior studies from our laboratory. Olivine grains from type IIA chondrules in CO chondrites and unequilibrated ordinary chondrites (UOC) have significantly different Fe/Mn ratios, with mean molar Fe/Mn = 99 and 44, respectively. Olivine analyses from both these chondrite groups show well‐defined trends in Mn versus Fe (afu) and molar Fe/Mn versus Fe/Mg diagrams. In general, type IIA chondrules in CR chondrites have properties intermediate between those in UOC and CO chondrites. In most UOC and CR type IIA chondrules, the Fe/Mn ratio of olivine decreases during crystallization, whereas in CO chondrites the Fe/Mn ratio does not appear to change. It is difficult to interpret the observed Fe/Mn trends in terms of differing moderately volatile element depletions inherited from precursor materials. Instead, we suggest that significant differences in the abundances of silicates and sulfides ± metals in the precursor material, as well as open‐system behavior during chondrule formation, were responsible for establishing the different Fe/Mn trends. Using Fe‐Mn‐Mg systematics, we are able to identify relict grains in type IIA chondrules, which could be derived from previous generations of chondrules, including chondrules from other chondrite groups, and possibly chondritic reservoirs that have not been sampled previously.  相似文献   

4.
Abstract— We report the results of an extensive study of the Fountain Hills chondritic meteorite. This meteorite is closely related to the CBa class. Mineral compositions and O‐isotopic ratios are indistinguishable from other members of this group. However, many features of Fountain Hills are distinct from the other CB chondrites. Fountain Hills contains 23 volume percent metal, significantly lower than other members of this class. In addition, Fountain Hills contains porphyritic chondrules, which are extremely rare in other CBa chondrites. Fountain Hills does not appear to have experienced the extensive shock seen in other CB chondrites. The chondrule textures and lack of fine‐grained matrix suggests that Fountain Hills formed in a dust‐poor region of the early solar system by melting of solid precursors. Refractory siderophiles and lithophile elements are present in near‐CI abundances (within a factor of two, related to the enhancement of metal). Moderately volatile and highly volatile elements are significantly depleted in Fountain Hills. The abundances of refractory siderophile trace elements in metal grains are consistent with condensation from a gas that is reduced relative to solar composition and at relatively high pressures (10?3bars). Fountain Hills experienced significant thermal metamorphism on its parent asteroid. Combining results from the chemical gradients in an isolated spinel grain with olivine‐spinel geothermometry suggests a peak temperature of metamorphism between 535 °C and 878 °C, similar to type‐4 ordinary chondrites.  相似文献   

5.
Abstract— We have studied the relationship between bulk chemical compositions and relative formation ages inferred from the initial 26Al/27Al ratios for sixteen ferromagnesian chondrules in least equilibrated ordinary chondrites, Semarkona (LL3.0) and Bishunpur (LL3.1). The initial 26Al/27Al ratios of these chondrules were obtained by Kita et al. (2000) and Mostefaoui et al. (2002), corresponding to relative ages from 0.7 ± 0.2 to 2.4 ?0.4/+0.7 Myr after calcium‐aluminum‐rich inclusions (CAIs), by assuming a homogeneous distribution of 26Al in the early solar system. The measured bulk compositions of the chondrules cover the compositional range of ferromagnesian chondrules reported in the literature and, thus, the chondrules in this study are regarded as representatives of ferromagnesian chondrules. The relative ages of the chondrules appear to correlate with bulk abundances of Si and the volatile elements (Na, K, Mn, and Cr), but there seems to exist no correlation of relative ages neither with Fe nor with refractory elements. Younger chondrules tend to be richer in Si and volatile elements. Our result supports the result of Mostefaoui et al. (2002) who suggested that pyroxene‐rich chondrules are younger than olivine‐rich ones. The correlation provides an important constraint on chondrule formation in the early solar system. It is explained by chondrule formation in an open system, where silicon and volatile elements evaporated from chondrule melts during chondrule formation and recondensed as chondrule precursors of the next generation.  相似文献   

6.
To better understand the formation conditions of ferromagnesian chondrules from the Renazzo‐like carbonaceous (CR) chondrites, a systematic study of 210 chondrules from 15 CR chondrites was conducted. The texture and composition of silicate and opaque minerals from each observed FeO‐rich (type II) chondrule, and a representative number of FeO‐poor (type I) chondrules, were studied to build a substantial and self‐consistent data set. The average abundances and standard deviations of Cr2O3 in FeO‐rich olivine phenocrysts are consistent with previous work that the CR chondrites are among the least thermally altered samples from the early solar system. Type II chondrules from the CR chondrites formed under highly variable conditions (e.g., precursor composition, redox conditions, cooling rate), with each chondrule recording a distinct igneous history. The opaque minerals within type II chondrules are consistent with formation during chondrule melting and cooling, starting as S‐ and Ni‐rich liquids at 988–1350 °C, then cooling to form monosulfide solid solution (mss) that crystallized around olivine/pyroxene phenocrysts. During cooling, Fe,Ni‐metal crystallized from the S‐ and Ni‐rich liquid, and upon further cooling mss decomposed into pentlandite and pyrrhotite, with pentlandite exsolving from mss at 400–600 °C. The composition, texture, and inferred formation temperature of pentlandite within chondrules studied here is inconsistent with formation via aqueous alteration. However, some opaque minerals (Fe,Ni‐metal versus magnetite and panethite) present in type II chondrules are a proxy for the degree of whole‐rock aqueous alteration. The texture and composition of sulfide‐bearing opaque minerals in Graves Nunataks 06100 and Grosvenor Mountains 03116 suggest that they are the most thermally altered CR chondrites.  相似文献   

7.
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   

8.
We investigated the matrix mineralogy in primitive EH3 chondrites Sahara 97072, ALH 84170, and LAR 06252 with transmission electron microscopy; measured the trace and major element compositions of Sahara 97072 matrix and ferromagnesian chondrules with laser‐ablation, inductively coupled, plasma mass spectrometry (LA‐ICPMS); and analyzed the bulk composition of Sahara 97072 with LA‐ICPMS, solution ICPMS, and inductively coupled plasma atomic emission spectroscopy. The fine‐grained matrix of EH3 chondrites is unlike that in other chondrite groups, consisting primarily of enstatite, cristobalite, troilite, and kamacite with a notable absence of olivine. Matrix and pyroxene‐rich chondrule compositions differ from one another and are distinct from the bulk meteorite. Refractory lithophile elements are enriched by a factor of 1.5–3 in chondrules relative to matrix, whereas the matrix is enriched in moderately volatile elements. The compositional relation between the chondrules and matrix is reminiscent of the difference between EH3 pyroxene‐rich chondrules and EH3 Si‐rich, highly sulfidized chondrules. Similar refractory element ratios between the matrix and the pyroxene‐rich chondrules suggest the fine‐grained material primarily consists of the shattered, sulfidized remains of the formerly pyroxene‐rich chondrules with the minor addition of metal clasts. The matrix, chondrule, and metal‐sulfide nodule compositions are probably complementary, suggesting all the components of the EH3 chondrites came from the same nebular reservoir.  相似文献   

9.
Abstract— We report detailed chemical, petrological, and mineralogical studies on the Ningqiang carbonaceous chondrite. Ningqiang is a unique ungrouped type 3 carbonaceous chondrite. Its bulk composition is similar to that of CV and CK chondrites, but refractory lithophile elements (1.01 × CI) are distinctly depleted relative to CV (1.29 × CI) and CK (1.20 × CI) chondrites. Ningqiang consists of 47.5 vol% chondrules, 2.0 vol% Ca,Al‐rich inclusions (CAIs), 4.5 vol% amoeboid olivine aggregates (AOAs), and 46.0 vol% matrix. Most chondrules (95%) in Ningqiang are Mg‐rich. The abundances of Fe‐rich and Al‐rich chondrules are very low. Al‐rich chondrules (ARCs) in Ningqiang are composed mainly of olivine, plagioclase, spinel, and pyroxenes. In ARCs, spinel and plagioclase are enriched in moderately volatile elements (Cr, Mn, and Na), and low‐Ca pyroxenes are enriched in refractory elements (Al and Ti). The petrology and mineralogy of ARCs in Ningqiang indicate that they were formed from hybrid precursors of ferromagnesian chondrules mixed with refractory materials during chondrule formation processes. We found 294 CAIs (55.0% type A, 39.5% spinel‐pyroxene‐rich, 4.4% hibonite‐rich, and several type C and anorthite‐spinel‐rich inclusions) and 73 AOAs in 15 Ningqiang sections (equivalent to 20 cm2surface area). This is the first report of hibonite‐rich inclusions in Ningqiang. They are texturally similar to those in CM, CH, and CB chondrites, and exhibit three textural forms: aggregates of euhedral hibonite single crystals, fine‐grained aggregates of subhedral hibonite with minor spinel, and hibonite ± Al,Ti‐diopside ± spinel spherules. Evidence of secondary alteration is ubiquitous in Ningqiang. Opaque assemblages, formed by secondary alteration of pre‐existing alloys on the parent body, are widespread in chondrules and matrix. On the other hand, nepheline and sodalite, existing in all chondritic components, formed by alkali‐halogen metasomatism in the solar nebula.  相似文献   

10.
Abstract– Nineteen nonporphyritic pyroxene and pyroxene/olivine chondrules, chondrule fragments, and irregular objects were studied from two equilibrated chondrites, the ordinary (L/LL5) Knyahinya chondrite and the Rumuruti type (R4) Ouzina chondrite. Major element contents for almost all objects in the chondrites are disturbed from their chondritic ratios, most probably during metamorphic re‐equilibration. However, the volatile elements (Na2O + K2O) in Ouzina scatter around the CI line, probably the result of being generated and/or processed in different environments as compared with those for Knyahinya. All studied objects from Knyahinya and Ouzina possess systematically fractionated trace element abundances. Depletion of LREE with respect to HREE and ultra‐refractory HFSE documents variable degrees of LREE transport into an external mineral sink and restricted mobility of most of the HREE and HFSE. Moderately volatile elements preserve volatility‐controlled abundances. Strongly fractionated Rb/Cs ratios (up to 10× CI) in all studied objects suggest restricted mobility of the large Cs ion. All studied objects sampled and preserved Y and Ho in solar proportions, a feature that they share with the nonporphyritic chondrules of unequilibrated ordinary chondrites.  相似文献   

11.
Cluster chondrites are characterized by close‐fit textures of deformed and indented chondrules, taken as evidence for hot chondrule accretion (Metzler 2012 ). We investigated seven cluster chondrite clasts from six brecciated LL3 chondrites and measured their bulk oxygen isotopic and chemical composition, including REE, Zr, and Hf. The same parameters were measured in situ on 93 chondrules and 4 interchondrule matrix areas. The CI‐normalized REE patterns of the clasts are flat, showing LL‐chondritic concentrations. The mean chemical compositions of chondrules in clasts and other LL chondrites are indistinguishable and we conclude that cluster chondrite chondrules are representative of the normal LL chondrule population. Type II chondrules are depleted in MgO, Al2O3 and refractory lithophiles (REE, Zr, Hf) by factors between 0.65 and 0.79 compared to type I chondrules. The chondrule REE patterns are basically flat with slight LREE < HREE fractionations. Many chondrules exhibit negative Eu anomalies while matrix shows a complementary pattern. Chondrules scatter along a correlation line with a slope of 0.63 in the oxygen 3‐isotope diagram, interpreted as the result of O‐isotope exchange between chondrule melts and 18O‐rich nebular components. In one clast, a distinct anticorrelation between chondrule size and δ18O is found, which may indicate a more intense oxygen isotope exchange by smaller chondrules. In some clasts the δ18O values of type I chondrules are correlated with concentrations of SiO2 and MnO and anticorrelated with MgO, possibly due to the admixture of a SiO2‐ and MnO‐rich component to chondrule melts during oxygen isotope exchange. Two chondrules with negative anomalies in Sm, Eu, and Yb were found and may relate their precursors to refractory material known from group III CAIs. Furthermore, three chondrules with strong LREE > HREE and Zr/Hf fractionations were detected, whose formation history remains to be explained.  相似文献   

12.
Abstract— I have determined the composition via instrumental neutron activation analysis of a bulk pristine sample of the Tagish Lake carbonaceous chondrite fall, along with bulk samples of the CI chondrite Orgueil and of several CM chondrites. Tagish Lake has a mean of refractory lithophile element/Cr ratios like those of CM chondrites, and distinctly higher than the CI chondrite mean. Tagish Lake exhibits abundances of the moderately volatile lithophile elements Na and K that are slightly higher than those of mean CM chondrites. Refractory through moderately volatile siderophile element abundances in Tagish Lake are like those of CM chondrites. Tagish Lake is distinct from CM chondrites in abundances of the most volatile elements. Mean CI‐normalized Se/Co, Zn/Co and Cs/Co for Tagish Lake are 0.68 ± 0.01, 0.71 ± 0.07 and 0.76 ± 0.02, while for all available CM chondrite determinations, these ratios lie between 0.31 and 0.61, between 0.32 and 0.58, and between 0.39 and 0.74, respectively. Considering petrography, and oxygen isotopic and elemental compositions, Tagish Lake is an ungrouped member of the carbonaceous chondrite clan. The overall abundance pattern is similar to those of CM chondrites, indicating that Tagish Lake and CMs experienced very similar nebular fractionations. Bells is a CM chondrite with unusual petrologic characteristics. Bells has a mean CI‐normalized refractory lithophile element/Cr ratio of 0.96, lower than for any other CM chondrite, but shows CI‐normalized moderately volatile lithophile element/Cr ratios within the ranges of other CM chondrites, except for Na which is low. Iridium, Co, Ni and Fe abundances are like those of CM chondrites, but the moderately volatile siderophile elements, Au, As and Sb, have abundances below the ranges for CM chondrites. Abundances of the moderately volatile elements Se and Zn of Bells are within the CM ranges. Bells is best classified as an anomalous CM chondrite.  相似文献   

13.
Abstract— Roosevelt County (RC) 075 was recovered in 1990 as a single 258-gram stone. Classification of this meteorite is complicated by its highly unequilibrated nature and its severe terrestrial weathering, but we favor H classification. This is supported by O isotopes and estimates of the original Fe, Ni metal content. The O isotopic composition is similar to that of a number of reduced ordinary chondrites (e.g., Cerro los Calvos, Willaroy), although RC 075 exhibits no evidence of reduced mineral compositions. Chondrule diameters are consistent with classification as an L chondrite, but large uncertainties in chondrule diameters of RC 075 and poorly constrained means of H, L and LL chondrites prevent use of this parameter for reliable classification. Other parameters are compromised by severe weathering (e.g., siderophile element abundances) or unsuitable for discrimination between unequilibrated H, L and LL chondrites (e.g., Co in kamacite, δ13C). Petrologic subtype 3.2± 0.1 is suggested by the degree of olivine heterogeneity, the compositions of chondrule olivines, the thermoluminescence sensitivity, the abundances and types of chondrules mapped on cathodoluminescence mosaics, and the amount of presolar SiC. The meteorite is very weakly shocked (S2), with some chondrules essentially unshocked and, thus, is classified as an H3.2(S2) chondrite. Weathering is evident by a LREE enrichment due to clay contamination, reduced levels of many siderophile elements, the almost total loss of Fe, Ni metal and troilite, and the reduced concentrations of noble gases. Some components of the meteorite (e.g., type IA chondrules, SiC) appear to preserve their nebular states, with little modification from thermal metamorphism. We conclude that RC 075 is the most unequilibrated H chondrite yet recovered and may provide additional insights into the origin of primitive materials in the solar nebula.  相似文献   

14.
Abstract— We present the first detailed study of a population of texturally distinct chondrules previously described by Kurat (1969), Christophe Michel‐Lévy (1976), and Skinner et al. (1989) that are sharply depleted in alkalis and Al in their outer portions. These “bleached” chondrules, which are exclusively radial pyroxene and cryptocrystalline in texture, have porous outer zones where mesostasis has been lost. Bleached chondrules are present in all type 3 ordinary chondrites and are present in lower abundances in types 4–6. They are most abundant in the L and LL groups, apparently less common in H chondrites, and absent in enstatite chondrites. We used x‐ray mapping and traditional electron microprobe techniques to characterize bleached chondrules in a cross section of ordinary chondrites. We studied bleached chondrules from Semarkona by ion microprobe for trace elements and H isotopes, and by transmission electron microscopy. Chondrule bleaching was the result of low‐temperature alteration by aqueous fluids flowing through finegrained chondrite matrix prior to thermal metamorphism. During aqueous alteration, interstitial glass dissolved and was partially replaced by phyllosilicates, troilite was altered to pentlandite, but pyroxene was completely unaffected. Calcium‐rich zones formed at the inner margins of the bleached zones, either as the result of the early stages of metamorphism or because of fluid‐chondrule reaction. The mineralogy of bleached chondrules is extremely sensitive to thermal metamorphism in type 3 ordinary chondrites, and bleached zones provide a favorable location for the growth of metamorphic minerals in higher petrologic types. The ubiquitous presence of bleached chondrules in ordinary chondrites implies that they all experienced aqueous alteration early in their asteroidal histories, but there is no relationship between the degree of alteration and metamorphic grade. A correlation between the oxidation state of chondrite groups and their degree of aqueous alteration is consistent with the source of water being either accreted ices or water released during oxidation of organic matter. Ordinary chondrites were probably open systems after accretion, and aqueous fluids may have carried volatile elements with them during dehydration. Individual radial pyroxene and cryptocrystalline chondrules were certainly open systems in all chondrites that experienced aqueous alteration leading to bleaching.  相似文献   

15.
Abstract— Anorthite‐rich chondrules in CR and CH carbonaceous chondrites consist of magnesian low‐Ca pyroxene and forsterite phenocrysts, FeNi‐metal nodules, interstitial anorthite, Al‐Ti‐Cr‐rich low‐Ca and high‐Ca pyroxenes, and crystalline mesostasis composed of silica, anorthite and high‐Ca pyroxene. Three anorthite‐rich chondrules contain relic calcium‐aluminum‐rich inclusions (CAIs) composed of anorthite, spinel, ±Al‐diopside, and ± forsterite. A few chondrules contain regions which are texturally and mineralogically similar to magnesian (type I) chondrules and consist of forsterite, low‐Ca pyroxene and abundant FeNi‐metal nodules. Anorthite‐rich chondrules in CR and CH chondrites are mineralogically similar to those in CV and CO carbonaceous chondrites, but contain no secondary nepheline, sodalite or ferrosilite. Relatively high abundances of moderately‐volatile elements such as Cr, Mn and Si in the anorthite‐rich chondrules suggest that these chondrules could not have been produced by volatilization of the ferromagnesian chondrule precursors or by melting of the refractory materials only. We infer instead that anorthite‐rich chondrules in carbonaceous chondrites formed by melting of the reduced chondrule precursors (olivine, pyroxenes, FeNi‐metal) mixed with the refractory materials, including relic CAIs, composed of anorthite, spinel, high‐Ca pyroxene and forsterite. The observed mineralogical and textural similarities of the anorthite‐rich chondrules in several carbonaceous chondrite groups (CV, CO, CH, CR) may indicate that these chondrules formed in the region(s) intermediate between the regions where CAIs and ferromagnesian chondrules originated. This may explain the relative enrichment of anorthite‐rich chondrules in 16O compared to typical ferromagnesian chondrules (Russell et al., 2000).  相似文献   

16.
Abstract— Petrographic and bulk compositional data suggest the existence of a new grouplet of carbonaceous chondrites consisting of Coolidge and Loongana 001. Coolidge is a carbonaceous chondrite find from Kansas, USA, previously considered a metamorphosed CV chondrite. Loongana 001 is a recent find from Western Australia. It has a high matrix/chondrule modal abundance ratio, 1–2 vol% refractory inclusions and high refractory lithophile abundance ratios (～1.35x CI), indicating that it is a carbonaceous chondrite. Coolidge and Loongana 001 have many compositional and petrographic similarities. They have refractory element abundances in the range of CV chondrites, significantly higher than those in the CR chondrites. They have similar volatile element abundance patterns showing low volatile element abundances relative to both CR and CV chondrites. Coolidge and Loongana 001 have similar chondrule dimensions and shapes, oxidation states and opaque mineral assemblages. They are also similar in petrologic type (3.8–4) and shock stage (S2). Although both Coolidge and Loongana 001 may be related to the CV clan, they are not CV chondrites, nor are they formed by metamorphism of a CV precursor. They are distinctly different in composition from CV chondrites and their chondrules are smaller and have a much lower abundance of coarse-grained chondrule rims. Coolidge and Loongana 001 constitute a distinct carbonaceous chondrite grouplet.  相似文献   

17.
Abstract— We carried out a petrologic and instrumental neutron activation analysis (INAA) whole chondrite compositional study of Grosvenor Mountains (GRO) 95577. GRO 95577 has many petrological similarities to the CR chondrites. Although the INAA data show patterns indicative of terrestrial weathering, some of the elemental abundances are consistent with a relationship to CR chondrites. The oxygen isotopic composition of GRO 95577 plots close to the Renazzo CR chondrite on the three‐isotope diagram. However, GRO 95577 is remarkable in that the chondrules are completely hydrated, consisting almost entirely of phyllosilicates, magnetite, and sulfides. Although GRO 95577 is completely hydrated, the initial chondrule textures are perfectly preserved. The chondrules are in sharp contact with the matrix, their fine‐grained rims are clearly visible, and the boundaries of the dark inclusions can be easily discerned. Many chondrules in GRO 95577 have textures suggestive of type I chondrules, but the phenocrysts have undergone perfect pseudomorphic replacement by yellow to brownish serpentine‐rich phyllosilicate, with sharp original crystal outlines preserved. The chondrule mesostasis is a green aluminous chlorite‐rich material, most likely a hydration product of the feldspathic mesostasis commonly found in anhydrous type I chondrules. Some chondrules contain magnetite spheres, most likely formed by oxidation of metal. We propose that GRO 95577 be classified as a CR1 chondrite, making it the first known CR1 chondrite and expanding the range of alteration conditions on the CR parent body.  相似文献   

18.
  相似文献   

19.
Sixteen nonporphyritic chondrules and chondrule fragments were studied in polished thin and thick sections in two enstatite chondrites (ECs): twelve objects from unequilibrated EH3 Sahara 97158 and four objects from equilibrated EH4 Indarch. Bulk major element analyses, obtained with electron microprobe analysis (EMPA) and analytical scanning electron microscopy (ASEM), as well as bulk lithophile trace element analyses, determined by laser ablation inductively coupled plasma–mass spectrometry (LA‐ICP‐MS), show that volatile components (K2O + Na2O versus Al2O3) scatter roughly around the CI line, indicating equilibration with the chondritic reservoir. All lithophile trace element abundances in the chondrules from Sahara 97158 and Indarch are within the range of previous analyses of nonporphyritic chondrules in unequilibrated ordinary chondrites (UOCs). The unfractionated (solar‐like) Yb/Ce ratio of the studied objects and the mostly unfractionated refractory lithophile trace element (RLTE) abundance patterns indicate an origin by direct condensation. However, the objects possess subchondritic CaO/Al2O3 ratios; superchondritic (Sahara 97158) and subchondritic (Indarch) Yb/Sc ratios; and chondritic‐normalized deficits in Nb, Ti, V, and Mn relative to RLTEs. This suggests a unique nebular process for the origin of these ECs, involving elemental fractionation of the solar gas by the removal of oldhamite, niningerite, and/or another phase prior to chondrule condensation. A layered chondrule in Sahara 97158 is strongly depleted in Nb in the core compared to the rim, suggesting that the solar gas was heterogeneous on the time scales of chondrule formation. Late stage metasomatic events produced the compositional diversity of the studied objects by addition of moderately volatile and volatile elements. In the equilibrated Indarch chondrules, this late process has been further disturbed, possibly by a postaccretional process (diffusion?) that preferentially mobilized Rb with respect to Cs in the studied objects.  相似文献   

20.
Abstract— The outer portions of many type I chondrules (Fa and Fs <5 mol%) in CR chondrites (except Renazzo and Al Rais) consist of silica‐rich igneous rims (SIRs). The host chondrules are often layered and have a porphyritic core surrounded by a coarse‐grained igneous rim rich in low‐Ca pyroxene. The SIRs are sulfide‐free and consist of igneously‐zoned low‐Ca and high‐Ca pyroxenes, glassy mesostasis, Fe, Ni‐metal nodules, and a nearly pure SiO2 phase. The high‐Ca pyroxenes in these rims are enriched in Cr (up to 3.5 wt% Cr2O3) and Mn (up to 4.4 wt% MnO) and depleted in Al and Ti relative to those in the host chondrules, and contain detectable Na (up to 0.2 wt% Na2O). Mesostases show systematic compositional variations: Si, Na, K, and Mn contents increase, whereas Ca, Mg, Al, and Cr contents decrease from chondrule core, through pyroxene‐rich igneous rim (PIR), and to SIR; FeO content remains nearly constant. Glass melt inclusions in olivine phenocrysts in the chondrule cores have high Ca and Al, and low Si, with Na, K, and Mn contents that are below electron microprobe detection limits. Fe, Ni‐metal grains in SIRs are depleted in Ni and Co relative to those in the host chondrules. The presence of sulfide‐free, SIRs around sulfide‐free type I chondrules in CR chondrites may indicate that these chondrules formed at high (>800 K) ambient nebular temperatures and escaped remelting at lower ambient temperatures. We suggest that these rims formed either by gas‐solid condensation of silica‐normative materials onto chondrule surfaces and subsequent incomplete melting, or by direct SiO(gas) condensation into chondrule melts. In either case, the condensation occurred from a fractionated, nebular gas enriched in Si, Na, K, Mn, and Cr relative to Mg. The fractionation of these lithophile elements could be due to isolation (in the chondrules) of the higher temperature condensates from reaction with the nebular gas or to evaporation‐recondensation of these elements during chondrule formation. These mechanisms and the observed increase in pyroxene/olivine ratio toward the peripheries of most type I chondrules in CR, CV, and ordinary chondrites may explain the origin of olivine‐rich and pyroxene‐rich chondrules in general.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号