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1.
Mean bulk chemical data of recently found H5 and L6 ordinary chondrites from the deserts of Oman generally reflect isochemical features which are consistent with the progressive thermal metamorphism of a common, unequilibrated starting material. Relative differences in abundances range from 0.5–10% in REE (Eu = 14%), 6–13% in siderophile elements (Co = 48%), and >10% in lithophile elements (exceptions are Ba, Sr, Zr, Hf, U = >30%) between H5 and L6 groups. These differences may have accounted for variable temperature conditions during metamorphism on their parent bodies. The CI/Mg‐normalized mean abundances of refractory lithophile elements (Al, Ca, Sm, Yb, Lu, V) show no resolvable differences between H5 and L6 suggesting that both groups have experienced the same fractionation. The REE diagram shows subtle enrichment in LREE with a flat HREE pattern. Furthermore, overall mean REE abundances are ~0.6 × CI with enriched La abundance (~0.9 × CI) in both groups. Precise oxygen isotope compositions demonstrate the attainment of isotopic equilibrium by progressive thermal metamorphism following a mass‐dependent isotope fractionation trend. Both groups show a ~slope‐1/2 line on a three‐isotope plot with subtle negative deviation in ?17O associated with δ18O enrichment relative to δ17O. These deviations are interpreted as the result of liberation of water from phyllosilicates and evaporation of a fraction of the water during thermal metamorphism. The resultant isotope fractionations caused by the water loss are analogous to those occurring between silicate melt and gas phase during CAI and chondrule formation in chondrites and are controlled by cooling rates and exchange efficiency.  相似文献   

2.
Abstract— Calcium, aluminum-rich inclusions (CAIs) are characteristic components in carbonaceous chondrites. Their mineralogy is dominated by refractory oxides and silicates like corundum, perovskite, spinel, hibonite, melilite, and Ca-pyroxene, which are predicted to be the first phases to have condensed from the cooling solar nebula. Allowing insights into processes occurring in the early solar system, CAIs in carbonaceous and ordinary chondrites were studied in great detail, whereas only a few refractory inclusions were found and studied in stratospheric interplanetary dust particles (IDPs) and micrometeorites. This study gives a summary of all previous studies on refractory inclusions in stratospheric IDPs and micrometeorites and will present new data on two Antarctic micrometeorites. The main results are summarized as follows: (a) Eight stratospheric IDPs and six micrometeorites contain Ca, Al-rich inclusions or refractory minerals. The constituent minerals include spinel, perovskite, fassaite, hibonite, melilite, corundum, diopside and anorthite. (b) Four of the seven obtained rare-earth-element (REE) patterns from refractory objects in stratospheric IDPs and micrometeorites are related to Group III patterns known from refractory inclusions from carbonaceous chondrites. A Group II related pattern was found for spinel and perovskite in two micrometeorites. The seventh REE pattern for an orthopyroxene is unique and can be explained by fractionation of Gd, Lu, and Tb at highly reducing conditions. (c) The O-isotopic compositions of most refractory objects in stratospheric IDPs and micrometeorites are similar to those of constituents from carbonaceous chondrites and fall on the carbonaceous chondrites anhydrous minerals mixing line. In fact, in most cases, in terms of mineralogy, REE pattern and O-isotopic composition of refractory inclusions in stratospheric IDPs and micrometeorites are in good agreement with a suggested genetic relation of dust particles and carbonaceous chondrites. Only in the case of one Antarctic micrometeorite does the REE pattern obtained for an orthopyroxene point to a link of this particle to enstatite chondrites.  相似文献   

3.
Abstract— We have determined Nb, Y, and Zr abundances in the carbonaceous chondrites Orgueil (CI), Murray (CM2), Murchison (CM2), Allende (CV3), and Karoonda (CK4), and in the eucrites, Pasamonte and Juvinas, by a recently developed spark source mass spectrometric technique using multiple ion counting (MIC‐SSMS). The abundance of Ta was determined in the same meteorites by radiochemical neutron activation analysis (RNAA). Precision of the MIC‐SSMS and RNAA techniques is ~3% and ≤ 5%, respectively. The new abundances for CI chondrites are: Nb = 0.247, Ta = 0.0142, Zr = 3.86, Y = 1.56 μg/g; or 0.699, 0.0202, 11.2, and 4.64 atoms/106 Si atoms, respectively. The values agree with earlier compilations, but they are a factor of 2 more precise than earlier analyses. Trace element concentrations in the CM, CV, and CK chondrites are higher than in the CI chondrite Orgueil by about 37, 86, and 120%, respectively, in agreement with the variable absolute contents of refractory lithophile elements in different groups of carbonaceous chondrites. Of particular interest are the chondritic Nb/Ta, Zr/Nb, and Nb/U ratios, because these ratios are important tools for interpreting the chemical evolution of planetary bodies. We obtained Nb/Ta = 17.4 ± 0.5 for the carbonaceous chondrites and the Juvinas‐type eucrites investigated. Though this value is similar to previous estimates, it is much more precise. The same is true for Zr/Nb (15.5 ± 0.2) and Zr/Y (2.32 ± 0.12). In combination with recently published MIC‐SSMS U data for carbonaceous chondrites, we obtained a chondritic Nb/U ratio of 29 ± 2. Because Nb, Ta, Zr, Y, and U are refractory lithophile elements and presumably partitioned into the silicate phase of the Earth during core formation, the elemental ratios may also be used to constrain evolution of the Earth's primitive mantle and, with the more precise determinations fractionation of Nb and Ta during magmatic processes and mantle‐crust interactions, can now be interpreted with greater confidence.  相似文献   

4.
Abstract— The cumulative mass distributions (mass range > 100 g) of each type of Japanese and U.S. Antarctic ordinary chondrites are compared with those of non-Antarctic falls and those obtained from the present-day flux of meteorites. The steeper slope of the mass distribution of Antarctic chondrites is indicative of the presence of several chondrite showers. The fall-to-specimen ratio of Antarctic ordinary chondrites larger than 100 g is about 1:2, indicating that half of them are shower components. The fall-to-specimen ratios of each group range from 1:1 to 1:6; those of the Japanese and U.S. Antarctic meteorite collections are 1:1 to 1:2 and 1:4 for H chondrites, 1:1 to 1:2 and 1:2 for L chondrites, and 1:2 and 1:6 for LL chondrites, indicating that the Japanese collection includes less abundant shower components than the U.S. collection. The fall-to-specimen ratios of each H4-6 and L4-6 type range from 1:1 to 1:4, and U.S. H6 and Japanese H4 have the low ratios of 1:4.  相似文献   

5.
Our survey of type 4–6 ordinary chondrites indicates that gas-poor, melt-rock and/or exotic clast-bearing fragmental breccias constitute 5%, 22% and 23%, respectively, of H, L and LL chondrites. These abundances contrast with the percentages of solar-gas-rich regolith breccias among ordinary chondrites: H (14%), L (3%) and LL (8%) (Crabb and Schultz, 1981). Petrologic study of several melt-rock-clast-bearing fragmental breccias indicates that some acquired their clasts prior to breccia metamorphism and others acquired them after metamorphism of host material. In general, the melt-rock clasts in gas-poor H chondrite fragmental breccias were acquired after breccia metamorphism and were probably formed by impacts into boulders or exposed outcrops of H4-6 material in the H chondrite parent body regolith. In contrast, most of the melt-rock clasts in gas-poor L and LL fragmental breccias were acquired prior to breccia metamorphism. The low abundance of regolith breccias among L chondrites and evidence that at least two-thirds of the L chondrites suffered a major shock event 0.5 Gyr ago, suggest that the L parent body may have been disrupted by a major collision at that time and that the remaining parent body fragments were too small to develop substantial regoliths (e.g., Heymann, 1967; Crabb and Schultz, 1981). Such a disruption would have exposed a large amount of L chondrite bedrock, some of which would consist of fragmental breccias that acquired melt-rock clasts very early in solar system history, prior to metamorphism. The exposed bedrock would serve as a potential target for sporadic meteoroid impacts to produce a few fragmental breccias with unmetamorphosed melt-rock clasts. The high proportion of genomict brecciated LL chondrites reflects a complex collisional history, probably including several episodes of parent body disruption and gravitational reassembly. Differences in the abundances of different kinds of breccias among the ordinary chondrite groups are probably due to the stochastic nature of major asteroidal collisions.  相似文献   

6.
The chemical effects of terrestrial alteration, with a particular focus on lithophile trace elements, were studied for a set of H chondrites displaying various degrees of weathering from fresh falls to altered finds collected from hot deserts. According to their trace element distributions, a considerable fraction of rare earth elements (REEs), Th, and U resides within cracks observed in weathered meteorite specimens. These cracks appear to accumulate unbound REEs locally accompanied by Th and U relative to the major element abundances, especially P and Si. The deposition of Ce is observed in cracks in the case of most of the weathered samples. Trace element maps visually confirm the accumulation of these elements in such cracks, as previously inferred based on chemical leaching experiments. Because the positive Ce anomalies and unbound REE depositions in cracks occur in all weathered samples studied here while none of such features are observed in less altered samples including falls (except for altered fall sample Nuevo Mercurio), these features are interpreted to have been caused by terrestrial weathering following chemical leaching. However, the overall effects on the bulk chemical composition remain limited as the data for all Antarctic meteorites studied in this work (except for heavily weathered sample A 09516, H6) are in good agreement with published data for unaltered meteorites.  相似文献   

7.
The Ca-phosphate phases in the Allende CV3 meteorite were selectively dissolved in ammoniacal EDTA solution and measured for abundances of the rare earth elements (REE) by radiochemical neutron activation and mass-spectrometric isotope dilution analyses. The REE abundances in CA-phosphates of Allende are remarkably different from those of ordinary chondrites. All the REE except Eu were observed to be enriched by factors of 50–100 relative to the C1 values. This is 3–4 times lower than concentrations of REE in the ordinary-chondrite phosphates. Allende phosphates have a small positive Eu anomaly, in contrast to the large negative Eu anomaly in phosphates from ordinary chondrites. Though the positive Eu anomaly in Allende Ca-phosphates is puzzling, the lack of a negative Eu anomaly in Allende Ca-phosphates suggests that they never have been in equilibrium with Allende coarse-grained Ca, Al-rich inclusions or their precursor materials.  相似文献   

8.
Abstract— Inductively coupled plasma mass spectrometry (ICP-MS) was successfully applied to bulk samples of Allende, Jilin, Modoc, Saint-Séverin and Atlanta for the determination of rare earth elements (REE) (Y and 14 lanthanoids), Th and U. The results of ICP-MS showed good agreement with recommended values, and their reproducibilities were high enough to discuss the detailed abundances of lanthanoids and actinoids in chondritic meteorites. For the Allende reference sample issued by the Smithsonian Institution, a positive anomaly of Tm, a fractionation between light REE and heavy REE and a high Th/U ratio were observed in the CI-normalized abundances of REE, Th and U. These features are common for group II inclusions in Allende, suggesting that the abundances of refractory lithophiles in Allende are somewhat influenced by those in a specific constituent. For the other chondritic meteorites, a zigzag alteration was commonly observed in the heavy-REE region of their CI-normalized abundance patterns. It is suggested that such a zigzag pattern is attributable to erratically high abundances of monoisotopic REE (Tb, Ho and Tm) in the CI values. Abundances of REE, Th and U in the bulk samples are also discussed separately in detail.  相似文献   

9.
Based on optical microscopy and electron microprobe analyses, eight previously undescribed or poorly known chondrites were classified into compositional groups, petrologic types, and degree of shock alteration. These chondrites are: Leander, L4b; Nazareth(a), L6d; La Villa, H4b; Mereta, H4c; Gail, H4d; Shafter Lake, H5a; Uvalde, H5d; and Howe, H5d.  相似文献   

10.
Abstract— Quantifying the peak temperatures achieved during metamorphism is critical for understanding the thermal histories of ordinary chondrite parent bodies. Various geothermometers have been used to estimate equilibration temperatures for chondrites of the highest metamorphic grade (type 6), but results are inconsistent and span hundreds of degrees. Because different geothermometers and calibration models were used with different meteorites, it is unclear whether variations in peak temperatures represent actual ranges of metamorphic conditions within type 6 chondrites or differences in model calibrations. We addressed this problem by performing twopyroxene geothermometry, using QUILF95, on the same type 6 chondrites for which peak temperatures were estimated using the plagioclase geothermometer (Nakamuta and Motomura 1999). We also calculated temperatures for published pyroxene analyses from other type 6 H, L, and LL chondrites to determine the most representative peak metamorphic temperatures for ordinary chondrites. Pyroxenes record a narrow, overlapping range of temperatures in H6 (865–926 °C), L6 (812–934 °C), and LL6 (874–945 °C) chondrites. Plagioclase temperature estimates are 96–179 °C lower than pyroxenes in the same type 6 meteorites. Plagioclase estimates may not reflect peak metamorphic temperatures because chondrule glass probably recrystallized to plagioclase prior to reaching the metamorphic peak. The average temperature for H, L, and LL chondrites (~900 °C), which agrees with previously published oxygen isotope geothermometry, is at least 50 °C lower than the peak temperatures used in current asteroid thermal evolution models. This difference may require minor adjustments to thermal model calculations.  相似文献   

11.
Olivine grains were analysed by microprobe for Si, Ca, Mg, and Fe. Distribution of Mg and Fe is similar to that already established for Type II and III carbonaceous chondrites. Calcium concentration varies by a factor of about 4 and seems to be independent of fayalite content: its range (about 0.1 ? 0.45 weight percent) resembles that in the olivines of Murray (Fredriksson and Keil, 1964). Olivines of carbonaceous chondrites are the product of mechanical mixing of pre-existing crystals (Van Schmus, 1969). More than one fractionation process is necessary to account for Ca variation superimposed on Mg:Fe fractionation observed in Murray, Murchison and Vigarano.  相似文献   

12.
The brecciation and shock classification of 2280 ordinary chondrites of the meteorite thin section collection at the Institut für Planetologie (Münster) has been determined. The shock degree of S3 is the most abundant shock stage for the H and LL chondrites (44% and 41%, respectively), while the L chondrites are on average more heavily shocked having more than 40% of rocks of shock stage S4. Among the H and LL chondrites, 40–50% are “unshocked” or “very weakly shocked.” Considering the petrologic types, in general, the shock degree is increasing with petrologic type. This is the case for all meteorite groups. The main criteria to define a rock as an S6 chondrite are the solid‐state recrystallization and staining of olivine and the melting of plagioclase often accompanied by the formation of high‐pressure phases like ringwoodite. These characteristics are typically restricted to local regions of a bulk chondrite in or near melt zones. In the past, the identification of high‐pressure minerals (e.g., ringwoodite) was often taken as an automatic and practical criterion for a S6 classification during chondrite bulk rock studies. The shock stage classification of many significantly shocked chondrites (>S3) revealed that most ringwoodite‐bearing rocks still contain more than 25% plagioclase (74%). Thus, these bulk chondrites do not even fulfill the S5 criterion (e.g., 75% of plagioclase has to be transformed into maskelynite) and have to be classified as S4. Studying chondrites on typically large thin sections (several cm2) and/or using samples from different areas of the meteorites, bulk chondrites of shock stage S6 should be extremely rare. In this respect, the paper will discuss the probability of the existence of bulk rocks of S6.  相似文献   

13.
Abstract— Zag is an H3‐6 chondrite regolith breccia within which we have studied 14 halite grains ≤3 mm. The purity of the associated NaCl‐H2O brine is implied by freezing characteristics of fluid inclusions in the halite and EPMA analyses together with a lack of other evaporite‐like phases in the Zag H3–6 component. This is inconsistent with multi‐stage evolution of the fluid involving scavenging of cations in the Zag region of the parent body. We suggest that the halite grains are clastic and did not crystallize in situ. Halite and water‐soluble extracts from Zag have light Cl isotopic compositions, δ37Cl = ?1.4 to ?2.8%. Previously reported bulk carbonaceous chondrite values are approximately δ37Cl = +3 to +4%. This difference is too great to be the result of fractionation during evaporation, and instead, we suggest that Cl isotopes in chondrites are fractionated between a light reservoir associated with fluids and a heavier reservoir associated with higher temperature phases such as phosphates and silicates. Extraterrestrial carbon released at 600 °C from the H3–4 matrix has δ13C = ?20%, consistent with poorly graphitized material being introduced into the matrix rather than indigenous carbonate derived from a brine. We have also examined 28 other H chondrite falls to ascertain how widespread halite or evaporite‐like mineral assemblages are in ordinary chondrites. We did not find any more to add to Zag (H3‐6) and Monahans (H5), which suggests that such highly soluble phases were not usually preserved on the parent bodies.  相似文献   

14.
Abstract— Compositions of four metal nodules from two ordinary chondrites, WIS91627 (H3.7) and Juin (H5), were determined by instrumental and radiochemical neutron activation analyses. Compared with bulk metal fractions, the metal nodules are characterized by strong and variable depletion of the refractory siderophile elements Re, Os, Ir, Ru, Pt and Rh but normal W and Mo, some fractionation of Co from Ni, and low Cu concentrations. These characteristics are difficult to explain by shock-induced vaporization followed by fractional condensation, a mechanism suggested by Widom et al. (1986). We propose formation of metal nodules during metamorphism in the parent body. Refractory siderophile elements, such as Ir, Os, Rh, etc., are partly locked up in noble metal nuggets and cannot participate in kamacite formation. The occurrence of metal nodules in both equilibrated and unequilibrated ordinary chondrites suggests that diffusion along grain boundaries was important in the development of kamacite and taenite in ordinary chondrites.  相似文献   

15.
Abstract— Oxygen‐isotopic compositions were determined for a suite of enstatite chondrites and aubrites. In agreement with previous work (Clayton et al., 1984), most samples have O‐isotopic compositions close to the terrestrial fractionation line (TFL), and there appear to be no significant differences in O‐isotopic compositions between individual EH and EL chondrites and aubrites. Five enstatite meteorites have O‐isotopic compositions that are significantly different from the other samples and >0.2% away from the TFL. Two of these have petrographic evidence of brecciation and interaction between other meteorite types; for the other three, similar scenarios are suggested. There appears to be a systematic increase in δ18O from enstatite chondrites (both EH and EL) of petrologic type 3 to those of type 6. There is also good evidence that the EH meteorites do not fall along a mass fractionation line but along a line slope 0.66. At the present time, detailed understanding of the origin of these O‐isotopic systematics remain elusive but clearly point to a complex accretion history, parent‐body evolution, or both.  相似文献   

16.
Nine twentieth-century ordinary chondrite falls from China are described and classified. They include: Nantong (H6), Zaoyang (H5), Zhaodong (L4), Qidong (L-LL5), Raoyang (L6), Sheyang (L6), Guangnan (L6), Suizhou (L6) and Nan Yang Pao (L6). Kamacite in Qidong is rare and contains much more Co (15 mg/g) than is characteristic of L-group chondrites; Qidong may be a member of a chondrite group intermediate in its properties between L and LL. Zhaodong, Qidong, Raoyang, Sheyang and Suizhou have several olivine and/or low-Ca pyroxene grains with aberrant Fel(Fe + Mg) ratios; it is probable that these five chondrites are fragmental breccias. The lack of correlation between shock facies and occurrence of aberrant silicate grains suggests that breccia lithification caused only minimal shock effects in many meteorites. Alternatively, postshock annealing may have resulted in the recrystallization of shock-indicating phases, leading to assignment of a shock facies that is lower than that present immediately after the shock event.  相似文献   

17.
Abstract— We have carried out a detailed petrographic, mineralogical, and trace element study of Northwest Africa (NWA) 011. This meteorite bears many similarities to the eucrites it was initially identified with, although oxygen isotopic compositions rule out a genetic relationship. Like many eucrites, NWA 011 crystallized from a source with approximately chondritic proportions of REE, although a slightly LREE‐enriched bulk composition with a small positive Eu anomaly, as well as highly fractionated Fe/Mg ratios and depleted Sc abundances (Korotchantseva et al. 2003), suggest that the NWA 011 source experienced some pyroxene and/or olivine fractionation. Thermal metamorphism resulted in homogenization of REE abundances within grains, but NWA 011 did not experience the intergrain REE redistribution seen in some highly metamorphosed eucrites. Despite a similarity in oxygen isotopic compositions, NWA 011 does not represent a basaltic partial melt from the acapulcoite/lodranite parent body. The material from which NWA 011 originated may have been like some CH or CB chondrites, members of the CR chondrite clan, which are all related through oxygen isotopic compositions. The NWA 011 parent body is probably of asteroidal origin, possibly the basaltic asteroid 1459 Magnya.  相似文献   

18.
The principal rock types in the highlands are highland basalt (gabbroic anorthosite) with 28% Al2O3 and low K Fra Mauro basalt with 18% Al2O3. The chemistry of the highland soils and breccias can be represented by simple mixing models involving these rock types as major constituents. The mixing occurred during the intense highland cratering. Layering observed at the Apennine Front is interpreted as produced the Serenitatis basin collision. The plains-forming Cayley Formation and the Descartes Formation are not volcanic, but are derived from pre-existing highland crust.Although the overall chemical composition of the Moon has been affected by pre-accretion processes (e.g. loss of volatile elements), the composition of the highlands is mainly the result of postaccretion melting and element fractionation. Thus the individual rock types show involatile element distribution patterns, relative to primitive abundances, indicative of solid-liquid equilibria, evidence of post-accretion lunar igneous activity.The chemistry of the primitive green glass component (15426) indicates that the abundance of the involatile elements (REE, Ba, Zr, Hf, Th and U) in the source regions is at most only 2–3 times the abundances in chondrites.Paper dedicated to Professor Harold C. Urey on the occasion of his 80th birthday on 29 April, 1973.  相似文献   

19.
High‐precision oxygen three‐isotope ratios were measured for four mineral phases (olivine, low‐Ca and high‐Ca pyroxene, and plagioclase) in equilibrated ordinary chondrites (EOCs) using a secondary ion mass spectrometer. Eleven EOCs were studied that cover all groups (H, L, LL) and petrologic types (4, 5, 6), including S1–S4 shock stages, as well as unbrecciated and brecciated meteorites. SIMS analyses of multiple minerals were made in close proximity (mostly <100 μm) from several areas in each meteorite thin section, to evaluate isotope exchange among minerals. Oxygen isotope ratios in each mineral become more homogenized as petrologic type increases with the notable exception of brecciated samples. In type 4 chondrites, oxygen isotope ratios of olivine and low‐Ca pyroxene are heterogeneous in both δ18O and Δ17O, showing similar systematics to those in type 3 chondrites. In type 5 and 6 chondrites, oxygen isotope ratios of the four mineral phases plot along mass‐dependent fractionation lines that are consistent with the bulk average Δ17O of each chondrite group. The δ18O of three minerals, low‐Ca and high‐Ca pyroxene and plagioclase, are consistent with equilibrium fractionation at temperatures of 700–1000 °C. In most cases the δ18O values of olivine are higher than those expected from pyroxene and plagioclase, suggesting partial retention of premetamorphic values due to slower oxygen isotope diffusion in olivine than pyroxene during thermal metamorphism in ordinary chondrite parent bodies.  相似文献   

20.
Abstract— Age patterns observed in meteorite groups reflect the different thermal or impact histories experienced by their parent bodies. To assess the number of ordinary chondrite (OC) parent bodies rare-gas data in the Schultz and Kruse (1989) data base were used to calculate U,Th-He gas-retention ages. Most H- and LL-chondrite ages are high; ~81% are >2.2 Ga. In contrast, most L-chondrite ages are low; ~69% are ≤2.2 Ga, and ~35% are ≤0.9 Ga. The latter fraction is substantially lower than the value of 44% given by Heymann (1967). The difference is attributed to the preferential inclusion of shocked L chondrites in early studies. Broad age peaks in the H and LL groups near 3.4 Ga probably reflect thermal loss during metamorphism, but in the H distribution there is a hint of minor outgassing “events” near 1 Ga. The L/LL chondrites have chemical properties intermediate between and unresolvable from L and LL chondrites. The high ages of most L/LL chondrites are evidence against these originating on the L parent body; the L/LL age distribution is consistent with an origin on the LL parent body or on an independent body.  相似文献   

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