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1.
Lithium abundances and isotope compositions are presented for a suite of sediments from the surroundings of the Ries Impact structure, paralleled by new Li data for central European tektites (moldavites) from several substrewn fields (South Bohemia, Moravia, Cheb Basin, Lusatia), including a specimen from the newly discovered substrewn field in Poland. The data set was supplemented by three clay fractions isolated from sedimentary samples. Moldavites measured in this study show a very narrow range in δ7Li values (?0.6 to 0.3‰ relative to L‐SVEC) and Li contents (23.9–48.1 ppm). This contrasts with sediments from the Ries area which show remarkable range in Li isotope compositions (from ?6.9 to 13.4‰) and Li contents (0.6–256 ppm). The OSM sediments which, based on chemical similarity, formed the major part of moldavites, show a range in δ7Li values from ?2.0 to 7.9‰ and Li contents from 5.8 to 78.9 ppm. Therefore, the formation of moldavites was apparently accompanied by large‐scale mixing, paralleled by chemical and isotope homogenization of their parent matter. The proposed Li mixing model indicates that sands, clayey sediments, and low volumes of carbonates are the major components for tektite formation whereas residual paleokarst sediments could have been a minor but important component for a subset of moldavites. Striking homogenization of Li in tektites, combined with limited Li loss during impacts, may suggest that moderately volatile elements are not scavenged and isotopically fractionated during large‐scale collisions, which is consistent with recent models. In general, whether homogenization of bodies with distinct Li isotope systematics takes place, or collision of bodies with similar Li systematics operates cannot be resolved at present stage but Li isotope homogeneity of solar system planets and asteroidal bodies tentatively implies the latter.  相似文献   

2.
Moldavites represent tektites derived from the Ries impact structure (~24 km diameter, ~15 Myr old) in southern Germany. Two new localities with parautochthonous moldavites in southwestern Poland were found. In these localities, fluvial sediments of the so‐called Gozdnicka formation host the moldavites. Characteristic tektite features, especially bubbles and inclusions of lechatelierite, are reported. The moldavites' size distribution and their abraded shapes indicate that they were redeposited from the nearby Lusatia substrewn field.  相似文献   

3.
Abstract— 40Ar/39Ar ages of four tektites (moldavites) from southern Bohemia (near ?eské Budějovice, Czech Republic) and a tektite from Lusatia (near Dresden, Germany) have been determined by 11 step‐degassing experiments. The purpose of the study was to enlarge the 40Ar/39Ar data base of moldavites and to check the age relations of the Bohemian and Lusatian samples. The mean plateau‐age of the Bohemian samples, which range from 14.42 to 14.70 Ma, is 14.50 ± 0.16 (0.42) (2σ) Ma (errors in parentheses include age error and uncertainty of standard monitor age). The plateau age of the Lusatian sample of 14.38 ± 0.26 (0.44) (2σ) Ma confirms the previously published 40Ar/39Ar age of 14.52 ± 0.08 (0.40) (2σ) Ma, and demonstrates that the fall of Lusatian and Bohemian tektites were contemporaneous. Because of their geochemistry and their ages there is no doubt that the Lusatian tektites are moldavites. Accepting that moldavites are ejecta from the Nördlinger Ries impact, the new ages also date the impact event. This age is slightly younger (about 0.2–0.3 Ma) than the age suggested by earlier K‐Ar determinations.  相似文献   

4.
Abstract— A new 40Ar/39Ar data set is presented for tektites from the Central European strewn field (moldavites). This is the only strewn field that is entirely situated in a continental environment and still characterized by scattered ages (14–15.3 Myr). The main objectives of the study were to define more precisely the moldavite formation age and provide a good calibration for a glass standard proposed for fission‐track dating. The laser total fusion ages obtained on chips from 7 individual specimens from the Southern Bohemian and Moravian subfields are restricted to a narrow interval of time, with an average of 14.34 ± 0.08 Myr relative to the 27.95 ± 0.09 Myr of the Fish Canyon Tuff biotite. This result gives a more precise age not only for the tektite field but also for its producing impact. If the genetic link between the moldavites and the Nördlinger Ries impact crater is maintained, then this new age has to be considered a reliable estimate for the Ries crater also. This new value places the formation of Central European tektites within the Lower Serravallian period in the latest geologic timescales. Evidence of their impact products, such as glass spherules or shocked minerals, can, therefore, be sought in sedimentary marine formations in a more precisely defined age interval.  相似文献   

5.
Abstract– The isotope fractionation of Zn in meteorites has been measured for the first time using thermal ionization mass spectrometry and a double spiking technique. The magnitude of δZn ranged from ?0.29 to +0.38‰ amu?1 for five stone meteorites whereas the iron meteorite Canyon Diablo displays δZn of 1.11 ± 0.11‰ amu?1. The results for chondrites in this work can be divided into positive and negative δZn, supporting a previous proposal that chondrites are a mixture of materials from two different temperature sources. The Zn isotope fractionation present in meteorites may represent a primordial heterogeneity formed in the early solar system. An anomalous isotopic composition of Zn obtained for the Redfields iron meteorite suggests large‐scale inherited isotope heterogeneity of the protosolar nebula, or the presence of a parent body that has formed within its own isotopically anomalous reservoir. These anomalies are in the same direction but smaller than nuclear field shift effects observed in chemical exchange reactions. The isotope dilution mass spectrometry (IDMS) technique was used to measure Zn concentration, yielding a range from 20.1 μg g?1 to 302 μg g?1 in five stone meteorites and from 0.019 to 26 μg g?1 in seven iron meteorites. The IDMS‐measured abundance of Zn in Orgueil is 302 ± 14 μg g?1 and should be considered for future compilations of the abundance of Zn in the solar system.  相似文献   

6.
Major and trace element analyses and triple oxygen isotope measurements were performed on 11 individual specimens of Australasian tektites (AAT) with exactly known field positions from Laos. The sample set was dominated by Muong Nong‐type tektites (MNAAT), including separated layers of glass of different appearance and chemistry from four samples. This first larger set of oxygen isotope data of MNAAT revealed the δ18O range 8.7 ≤ δ18O ≤ 11.6‰ on VSMOW2 scale (12 analyses), only slightly wider than the previously reported range for splash‐form AAT. The Δ’17O values of MNAAT (?0.098 ≤ Δ’17O ≤ ?0.069‰; 12 analyses) and splash‐form AAT (?0.080 ≤ Δ’17O ≤ ?0.068‰; three analyses) are all in the range of data typical for terrestrial crustal rocks, with no mass‐independent oxygen isotope fractionation (from impactor or from exchange with atmospheric O2) being observed.  相似文献   

7.
Abstract— Using detailed geological, petrographic, geochemical, and geographical constraints we have performed numerical modeling studies that relate the Steinheim crater (apparent diameter Da = 3.8 km), the Ries crater (Da = 24 km) in southern Germany, and the moldavite (tektite) strewn field in Bohemia and Moravia (Czech Republic), Lusatia (East Germany), and Lower Austria. The moldavite strewn field extends from ～200 to 450 km from the center of the Ries to the east‐northeast forming a fan with an angle of ～57°. An oblique impact of a binary asteroid from a west‐southwest direction appears to explain the locations of the craters and the formation and distribution of the moldavites. The impactor must have been a binary asteroid with two widely separated components (some 1.5 and 0.15 km in diameter, respectively). We carried out a series of three‐dimensional hydrocode simulations of a Ries‐type impact. The results confirm previous results suggesting that impacts around 30–50° (from the horizontal) are the most favorable angles for near‐surface melting, and, consequently for the formation of tektites. Finally, modeling of the motion of impact‐produced tektite particles through the atmosphere produces, in the downrange direction, a narrow‐angle distribution of the moldavites tektites in a fan like field with an angle of ～75°. An additional result of modeling the motion of melt inside and outside the crater is the preferred flow of melt from the main melt zone of the crystalline basement downrange towards the east‐northeast rim. This explains perfectly the occurrence of coherent impact melt bodies (some tens of meters in size) in a restricted zone of the downrange rim of the Ries crater. The origin of these melt bodies, which represent chemically a mixture of crystalline basement rocks similar to the main melt mass contained (as melt particles <0.5 m in size) in the suevite, do not occur at any other portion of the Ries crater rim and remained enigmatic until now. Although the calculated distribution of moldavites still deviates to some degree from the known distribution, our results represent an important step toward a better understanding of the origin and distribution of the high‐velocity surface melts and the low‐velocity, deep‐seated melt resulting from an oblique impact on a stratified target.  相似文献   

8.
Abstract– High‐precision Cu isotopic compositions have been measured for the metal phase of 29 iron meteorites from various groups and for four terrestrial standards. The data are reported as the δ65Cu permil deviation of the 65Cu/63Cu ratio relative to the NIST SRM 976 standard. Terrestrial mantle rocks have a very narrow range of variations and scatter around zero. In contrast, iron meteorites show δ65Cu approximately 2.3‰ variations. Different groups of iron meteorites have distinct δ65Cu values. Nonmagmatic IAB‐IIICD iron meteorites have similar δ65Cu (0.03 ± 0.08 and 0.12 ± 0.10, respectively), close to terrestrial values (approximately 0). The other group of nonmagmatic irons, IIE, is isotopically distinct (?0.69 ± 0.15). IVB is the iron meteorite group with the strongest elemental depletion in Cu and samples in this group are enriched in the lighter isotope (δ65Cu down to ?2.26‰). Evaporation should have produced an enrichment in 65Cu over 63Cu (δ65Cu >0) and can therefore be ruled out as a mechanism for volatile loss in IVB meteorites. In silicate‐bearing iron meteorites, Δ17O correlates with δ65Cu. This correlation between nonmass‐dependent and mass‐dependent parameters suggests that the Cu isotopic composition of iron meteorites has not been modified by planetary differentiation to a large extent. Therefore, Cu isotopic ratios can be used to confirm genetic links. Cu isotopes thus confirm genetic relationships between groups of iron meteorites (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites). Several genetic connections between iron meteorites groups are confirmed by Cu isotopes, (e.g., IAB and IIICD; IIIE and IIIAB); and between iron meteorites and chondrites (e.g., IIE and H chondrites).  相似文献   

9.
High‐precision Zn isotopic compositions measured by MC‐ICP‐MS are documented for 32 iron meteorites from various fractionally crystallized and silicate‐bearing groups. The δ66Zn values range from ?0.59‰ up to +5.61‰ with most samples being slightly enriched in the heavier isotopes compared with carbonaceous chondrites (0 < δ66Zn < 0.5). The δ66Zn versus δ68Zn plot of all samples defines a common linear fractionation line, which supports the hypothesis that Zn was derived from a single reservoir or from multiple reservoirs linked by mass‐dependent fractionation processes. Our data for Redfields fall on a mass fractionation line and therefore refute a previous claim of it having an anomalous isotopic composition due to nonmixing of nucleosynthetic products. The negative correlation between δ66Zn and the Zn concentration of IAB and IIE is consistent with mass‐dependent isotopic fractionation due to evaporation with preferential loss of lighter isotopes in the vapor phase. Data for the Zn concentrations and isotopic compositions of two IVA samples demonstrate that volatile depletion in the IVA parent body is not likely the result of evaporation. This is important evidence that favors the incomplete condensation origin for the volatile depletion of the IVA parent body.  相似文献   

10.
Abstract– We present NanoSIMS four‐isotope S analyses of 24 comet Wild 2 dust impact residues in craters on aluminum foil C2037N returned by NASA’s Stardust mission. Except for one sample, all impact residues have normal S isotopic compositions within 2σ uncertainties of at least two S isotope ratios. This implies that most S‐rich Wild 2 dust impactors formed in the solar system. Instrumental isotope fractionation due to sample topography is the main contribution to our analytical uncertainty. One impact crater residue shows small anomalies of δ33S = ?57 ± 17‰, and δ34S = ?41 ± 17‰ (1σ uncertainties). Although this could be simply a statistical outlier or the fingerprint of a chemical isotope fractionation it is also possible that the observed anomaly results from the mixture of a cometary FeS particle with a small (150 nm diam.) presolar FeS supernova grain. This would translate into a presolar sulfide abundance of approximately 200 ppm.  相似文献   

11.
Seven impact melts from various places in the Nördlinger Ries were dated by 40Ar‐39Ar step‐heating. The aim of these measurements was to increase the age data base for Ries impact glasses directly from the Ries crater, because there is only one Ar‐Ar step‐heating spectrum available in the literature. Almost all samples display saddle‐shaped age spectra, indicating the presence of excess argon in most Ries glass samples, most probably inherited argon from incompletely degassed melt and possibly also excess argon incorporated during cooling from adjacent phases. In contrast, moldavites usually contain no inherited argon, probably due to their different formation process implying solidification during ballistic transport. The plateau age of the only flat spectrum is 14.60 ± 0.16 (0.20) Ma (2σ), while the total age of this sample is 14.86 ± 0.20 (0.22) Ma (isochron age: 14.72 ± 0.18 [0.22] Ma [2σ]), proofing the chronological relationship of the Ries impact and moldavites. The total ages of the other samples range between 15.77 ± 0.52 and 20.4 ± 1.0 Ma (2σ), implying approximately 2–40% excess 40Ar (compared to the nominal age of the Ries crater) in respective samples. Thus, the age of 14.60 ± 0.16 (0.20) (2σ) (14.75 ± 0.16 [0.20 Ma] [2σ], calculated using the most recent suggestions for the K decay constants) can be considered as reliable and is within uncertainties indistinguishable from the most recent compilation for the age of the moldavite tektites.  相似文献   

12.
We report the first occurrence of moldavites in Poland. This discovery confirms the hypothesis that moldavites could have been distributed up to 500 km from the Ries crater in Germany. The tektites were reworked from Middle Miocene sediments and redeposited in Late Miocene (Pannonian) fluvial deposits of the Gozdnicka Formation in Lower Silesia. The Polish moldavites are represented by nine (<8 mm) fragments with a total of 0.471 g. The lack of the autochthonous tektites indicates that tektites investigated here had to be redeposited in a fluvial environment, probably from the Lusatian area. The chemical composition of the Polish moldavites plots in the same area with those from other localities.  相似文献   

13.
Abstract– Tektites, natural silica‐rich glasses produced during impact events, commonly contain bubbles. The paper reviews published data on pressure and composition of a gas phase contained in the tektite bubbles and data on other volatile compounds which can be released from tektites by either high‐temperature melting or by crushing or milling under vacuum. Gas extraction from tektites using high‐temperature melting generally produced higher gas yield and different gas composition than the low‐temperature extraction using crushing or milling under vacuum. The high‐temperature extraction obviously releases volatiles not only from the bubbles, but also volatile compounds contained directly in the glass. Moreover, the gas composition can be modified by reactions between the released gases and the glass melt. Published data indicate that besides CO2 and/or CO in the bubbles, another carbon reservoir is present directly in the tektite glass. To clarify the problem of carbon content and carbon isotopic composition of the tektite glass, three samples from the Central European tektite strewn field—moldavites—were analyzed. The samples contained only 35–41 ppm C with δ13C values in the range from ?28.5 to ?29.9‰ VPDB. This indicates that terrestrial organic matter was a dominant carbon source during moldavite formation.  相似文献   

14.
Rhenium is an important element with which to test hypotheses of isotope variation. Historically, it has been difficult to precisely correct the instrumental mass bias in thermal ionization mass spectrometry. We used W as an internal standard to correct mass bias on the MC‐ICP‐MS, and obtained the first precise δ187Re values (~±0.02‰, 2SE) for iron meteorites and chondritic metal. Relative to metal from H chondrites, IVB irons are systematically higher in δ187Re by ~0.14 ‰. δ187Re for other irons are similar to H chondritic metal, although some individual samples show significant isotope fractionation. Since 185Re has a high neutron capture cross section, the effect of galactic cosmic‐ray (GCR) irradiation on δ187Re was examined using correlations with Pt isotopes. The pre‐GCR irradiation δ187Re for IVB irons is lower, but the difference in δ187Re between IVB irons and other meteoritic metal remains. Nuclear volume‐dependent fractionation for Re is about the right magnitude near the melting point of iron, but because of the refractory and compatible character of Re, a compelling explanation in terms of mass‐dependent fractionation is elusive. The magnitude of a nucleosynthetic s‐process deficit for Re estimated from Mo and Ru isotopes is essentially unresolvable. Since thermal processing reduced nucleosynthetic effects in Pd, it is conceivable that Re isotopic variations larger than those in Mo and Ru may be present in IVBs since Re is more refractory than Mo and Ru. Thus, the Re isotopic difference between IVBs and other irons or chondritic metal remains unexplained.  相似文献   

15.
Abstract— Twenty‐three moldavites from a new locality, the Cheb Basin in Western Bohemia, were analyzed by instrumental neutron activation analysis for 45 major and trace elements. Detailed comparison of the Cheb Basin moldavites with moldavites from other substrewn fields in both major and trace element composition shows that the Cheb Basin is a separate substrewn field. The geochemical data obtained are discussed with respect to the source materials and processes leading to formation of moldavites. The data show that three groups of Cheb Basin moldavites exist. Ten samples of group 1 are characterized by the lowest content of Al, Fe, Na, and other elements representing phyllosilicate minerals, and by high Ca + Mg contents related probably to carbonates. They resemble the “poisonous green” moldavites, a subgroup of the Southern Bohemian moldavites. Seven samples of group 2 and 6 samples of group 3 are similar to typical moldavites of the Southern Bohemian substrewn field. These two groups differ from each other mainly in Al contents; with higher contents of Al and the elements associated with phyllosilicate minerals (namely Ba and Sr), group 3 also resembles the Moravian moldavites. Significant positive correlations between K, Ca, Mg, and Mn found in group 2 of the Cheb Basin moldavites and the enrichment in these elements observed generally in all moldavites, as well as other facts, e.g., high K/Na and K/Rb ratios and the reduced conditions during formation of moldavites, have been attributed to possible contribution to the moldavite source materials of the ash produced by burning of vegetation and soil organic matter present at the pre‐impact area.  相似文献   

16.
Meteorite fusion crust formation is a brief event in a high‐temperature (2000–12,000 K) and high‐pressure (2–5 MPa) regime. We studied fusion crusts and bulk samples of 10 ordinary chondrite falls and 10 ordinary chondrite finds. The fusion crusts show a typical layering and most contain vesicles. All fusion crusts are enriched in heavy Fe isotopes, with δ56Fe values up to +0.35‰ relative to the solar system mean. On average, the δ56Fe of fusion crusts from finds is +0.23‰, which is 0.08‰ higher than the average from falls (+0.15‰). Higher δ56Fe in fusion crusts of finds correlate with bulk chondrite enrichments in mobile elements such as Ba and Sr. The δ56Fe signature of meteorite fusion crusts was produced by two processes (1) evaporation during atmospheric entry and (2) terrestrial weathering. Fusion crusts have either the same or higher δ18O (0.9–1.5‰) than their host chondrites, and the same is true for Δ17O. The differences in bulk chondrite and fusion crust oxygen isotope composition are explained by exchange of oxygen between the molten surface of the meteorites with the atmosphere and weathering. Meteorite fusion crust formation is qualitatively similar to conditions of chondrule formation. Therefore, fusion crusts may, at least to some extent, serve as a natural analogue to chondrule formation processes. Meteorite fusion crust and chondrules exhibit a similar extent of Fe isotope fractionation, supporting the idea that the Fe isotope signature of chondrules was established in a high‐pressure environment that prevented large isotope fractionations. The exchange of O between a chondrule melt and an 16O‐poor nebula as the cause for the observed nonmass dependent O isotope compositions in chondrules is supported by the same process, although to a much lower extent, in meteorite fusion crusts.  相似文献   

17.
Lithium isotope and abundance data are reported for Apollo 15 and 17 mare basalts and the LaPaz low‐Ti mare basalt meteorites, along with lithium isotope data for carbonaceous, ordinary, and enstatite chondrites, and chondrules from the Allende CV3 meteorite. Apollo 15 low‐Ti mare basalts have lower Li contents and lower δ7Li (3.8 ± 1.2‰; all uncertainties are 2 standard deviations) than Apollo 17 high‐Ti mare basalts (δ7Li = 5.2 ± 1.2‰), with evolved LaPaz mare basalts having high Li contents, but similar low δ7Li (3.7 ± 0.5‰) to Apollo 15 mare basalts. In low‐Ti mare basalt 15555, the highest concentrations of Li occur in late‐stage tridymite (>20 ppm) and plagioclase (11 ± 3 ppm), with olivine (6.1 ± 3.8 ppm), pyroxene (4.2 ± 1.6 ppm), and ilmenite (0.8 ± 0.7 ppm) having lower Li concentrations. Values of δ7Li in low‐ and high‐Ti mare basalt sources broadly correlate negatively with 18O/16O and positively with 56Fe/54Fe (low‐Ti: δ7Li ≤4‰; δ56Fe ≤0.04‰; δ18O ≥5.7‰; high‐Ti: δ7Li >6‰; δ56Fe >0.18‰; δ18O <5.4‰). Lithium does not appear to have acted as a volatile element during planetary formation, with subequal Li contents in mare basalts compared with terrestrial, martian, or vestan basaltic rocks. Observed Li isotopic fractionations in mare basalts can potentially be explained through large‐degree, high‐temperature igneous differentiation of their source regions. Progressive magma ocean crystallization led to enrichment in Li and δ7Li in late‐stage liquids, probably as a consequence of preferential retention of 7Li and Li in the melt relative to crystallizing solids. Lithium isotopic fractionation has not been observed during extensive differentiation in terrestrial magmatic systems and may only be recognizable during extensive planetary magmatic differentiation under volatile‐poor conditions, as expected for the lunar magma ocean. Our new analyses of chondrites show that they have δ7Li ranging between ?2.5‰ and 4‰. The higher δ7Li in planetary basalts than in the compilation of chondrites (2.1 ± 1.3‰) demonstrates that differentiated planetary basalts are, on average, isotopically heavier than most chondrites.  相似文献   

18.
We present high‐precision measurements of the Mg isotopic compositions of a suite of types I and II chondrules separated from the Murchison and Murray CM2 carbonaceous chondrites. These chondrules are olivine‐ and pyroxene‐rich and have low 27Al/24Mg ratios (0.012–0.316). The Mg isotopic compositions of Murray chondrules are on average lighter (δ26Mg ranging from ?0.95‰ to ?0.15‰ relative to the DSM‐3 standard) than those of Murchison (δ26Mg ranging from ?1.27‰ to +0.77‰). Taken together, the CM2 chondrules exhibit a narrower range of Mg isotopic compositions than those from CV and CB chondrites studied previously. The least‐altered CM2 chondrules are on average lighter (average δ26Mg = ?0.39 ± 0.30‰, 2SE) than the moderately to heavily altered CM2 chondrules (average δ26Mg = ?0.11 ± 0.21‰, 2SE). The compositions of CM2 chondrules are consistent with isotopic fractionation toward heavy Mg being associated with the formation of secondary silicate phases on the CM2 parent body, but were also probably affected by volatilization and recondensation processes involved in their original formation. The low‐Al CM2 chondrules analyzed here do not exhibit any mass‐independent variations in 26Mg from the decay of 26Al, with the exception of two chondrules that show only small variations just outside of the analytical error. In the case of the chondrule with the highest Al/Mg ratio (a type IAB chondrule from Murchison), the lack of resolvable 26Mg excess suggests that it either formed >1 Ma after calcium‐aluminum‐rich inclusions, or that its Al‐Mg isotope systematics were reset by secondary alteration processes on the CM2 chondrite parent body after the decay of 26Al.  相似文献   

19.
We determined the chlorine isotope composition of 16 Martian meteorites using gas source mass spectrometry on bulk samples and in situ secondary ion microprobe analysis on apatite grains. Measured δ37Cl values range from ?3.8 to +8.6‰. The olivine‐phyric shergottites are the isotopically lightest samples, with δ37Cl mostly ranging from ?4 to ?2‰. Samples with evidence for a crustal component have positive δ37Cl values, with an extreme value of 8.6‰. Most of the basaltic shergottites have intermediate δ37Cl values of ?1 to 0‰, except for Shergotty, which is similar to the olivine‐phyric shergottites. We interpret these data as due to mixing of a two‐component system. The first component is the mantle value of ?4 to ?3‰. This most likely represents the original bulk Martian Cl isotope value. The other endmember is a 37Cl‐enriched crustal component. We speculate that preferential loss of 35Cl to space has resulted in a high δ37Cl value for the Martian surface, similar to what is seen in other volatile systems. The basaltic shergottites are a mixture of the other two endmembers. The low δ37Cl value of primitive Mars is different from Earth and most chondrites, both of which are close to 0‰. We are not aware of any parent‐body process that could lower the δ37Cl value of the Martian mantle to ?4 to ?3‰. Instead, we propose that this low δ37Cl value represents the primordial bulk composition of Mars inherited during accretion. The higher δ37Cl values seen in many chondrites are explained by later incorporation of 37Cl‐enriched HCl‐hydrate.  相似文献   

20.
We report precise triple oxygen isotope data of bulk materials and separated fractions of several Shergotty–Nakhla–Chassigny (SNC) meteorites using enhanced laser‐assisted fluorination technique. This study shows that SNCs have remarkably identical Δ17O and a narrow range in δ18O values suggesting that these meteorites have assimilated negligibly small surface materials (<5%), which is undetectable in the oxygen isotope compositions reported here. Also, fractionation factors in coexisting silicate mineral pairs (px‐ol and mask‐ol) further demonstrate isotopic equilibrium at magmatic temperatures. We present a mass‐dependent fractionation line for bulk materials with a slope of 0.526 ± 0.016 (1SE) comparable to the slope obtained in an earlier study (0.526 ± 0.013; Franchi et al. 1999). We also present a new Martian fractionation line for SNCs constructed from separated fractions (i.e., pyroxene, olivine, and maskelynite) with a slope of 0.532 ± 0.009 (1SE). The identical fractionation lines run above and parallel to our terrestrial fractionation line with Δ17O = 0.318 ± 0.016‰ (SD) for bulk materials and 0.316 ± 0.009‰ (SD) for separated fractions. The conformity in slopes and Δ17O between bulk materials and separated fractions confirm oxygen isotope homogeneity in the Martian mantle though recent studies suggest that the Martian lithosphere may potentially have multiple oxygen isotope reservoirs.  相似文献   

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