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1.
Abstract— The C contents and isotopic compositions of four eucrites, four diogenites and two howardites have been determined. Stepped heating in an O atmosphere was employed to convert selectively different carbonaceous materials to CO2 gas at various temperatures. This technique successfully distinguishes between terrestrial contaminants and indigenous C. With the exception of the Kapoeta howardite, the howardite, eucrite, and diogenite (HED) meteorites contain ～10–30 ppm indigenous C with δ13C between ?29% and ?19%. Kapoeta (a regolith breccia) has an elevated C content and δ13C, due to the presence of 13C-enriched carbonate minerals (δ13C ～ +20%) in CM2- or CR2-like clasts. The range in δ13C displayed by HED samples is similar to that of other solar system basalts, such as lunar rocks and Martian meteorites but distinctly different from that of the terrestrial mantle. The diogenites have a slightly lower total C yield and higher δ13C than the eucrites, which is a result of degassing of trapped CO/CC2/CO2–3 from the silicate lattice during metamorphism or annealing. However, three out of the four diogenites studied appear to contain a discrete component, possibly of graphitic C coating silicate grains, that is seemingly unaffected by the extended annealing period experienced by the diogenites. It is possible that this component might host the indigenous primitive Xe recently identified in diogenites.  相似文献   

2.
Abstract— The nature and isotopic composition of carbonaceous components in a variety of ordinary chondrites have been studied using stepped combustion. The samples were chosen to include falls, finds and Antarctic meteorites; specimens from all three chemical groups (H, L and LL) have been analysed. Effort was concentrated mostly on the low petrologic type meteorites (i.e., type 3); however, types 4–6 were also included in the study. Apart from terrestrial contaminants and weathering products, some of the unequilibrated ordinary chondrites appear to contain an indigenous organic component. In addition, most of the samples studied show evidence for an amorphous/graphitic component. This exists as C-rich aggregates or as carbon associated with “Huss” matrix. There does not appear to be any difference in δ13C for this carbon between Antarctic and non-Antarctic meteorites. In contrast, low temperature carbon in Antarctic samples is characterized by a 13C-enrichment. This is thought to be due to the influence of terrestrial weathering products introduced in the Antarctic. Curiously, the low temperature carbon in non-Antarctic finds appears to be intermediate in δ13C between Antarctic finds and non-Antarctic falls. This suggests that the weathering processes which are so obviously apparent from Antarctic samples may also extend, albeit in a more limited way, to non-Antarctic meteorites.  相似文献   

3.
Abstract— The Sahara Desert is a region of high diurnal temperature variation and sporadic rainfall that has recently yielded over 450 meteorites. Eighteen of these Saharan samples are carbonaceous chondrites, of which we have analysed 17 for C content and isotopic composition. Ten of the 18 are paired CR chondrites, of which four have also had N and H contents and compositions determined. A primitive ordinary chondrite (L/LL3.2) found in the region has also been analysed for C, N and H contents and isotopic composition. Saharan samples contain between 21% and 45% of the light elements of their non-Saharan counterparts. Paired Saharan samples show a greater heterogeneity in both C content and isotopic composition than multiple analyses of non-Saharan samples. The cause of the observed isotopic and abundance effects is due to the hot desert weathering processes experienced by these samples. Peak temperatures of meteorites on the desert floor may be in excess of 100 °C, leading to low-temperature hydrous pyrolysis and oxidation reactions, liberating volatile organics and CO2. This may also cause the remaining material to become partially solubilised and ultimately lost during rainfall. The low δD of the CR and ordinary chondrites can be attributed to the destruction and loss of organic material through dehydrogenation and exchange reactions on the desert surface. The increased 13C abundance suggests that the less tightly bound C from the macromolecular organic material is isotopically lighter than the remaining C. Carbon contents and isotopic compositions are also affected by the addition of terrestrial calcitic evaporite deposits, up to 10,000 ppm carbonate has been measured, with a δ13C of between 0 and ?10%0.  相似文献   

4.
Abstract— Micrometeorites (MMs) currently represent the largest steady‐state mass flux of extraterrestrial matter to Earth and may have delivered a significant fraction of volatile elements and organics to the Earth's surface. Nitrogen and noble gases contents and isotopic ratios have been measured in a suite of 17 micrometeorites recovered in Antarctica (sampled in blue ice at Cap Prudhomme) and Greenland (separated from cryoconite) that have experienced variable thermal metamorphism during atmospheric entry. MMs were pyrolized using a CO2 laser and the released gases were analyzed for nitrogen and noble gas abundances and isotopic ratios by static mass spectrometry after specific purification. Noble gases are a mixture of cosmogenic, solar, atmospheric, and possibly chondritic components, with atmospheric being predominant in severely heated MMs. δ15N values vary between ?240 ± 62‰ and +206 ± 12‰, with most values being within the range of terrestrial and chondritic signatures, given the uncertainties. Crystalline MMs present very high noble gas contents up to two orders of magnitude higher than carbonaceous chondrite concentrations. In contrast, nitrogen contents between 4 ppm and 165 ppm are much lower than those of carbonaceous chondrites, evidencing either initially low N content in MMs and/or degradation of phases hosting nitrogen during atmospheric entry heating and terrestrial weathering. Assuming that the original N content of MMs was comparable to that of carbonaceous chondrites, the contribution of nitrogen delivery by these objects to the terrestrial environment would have been probably marginal from 3.8 Gyr ago to present but could have been significant (?10%) in the Hadean, and even predominant during the latest stages of terrestrial accretion.  相似文献   

5.
In this study, we present a method for high precision Δ′17O (Δ′17ORL = ln(δ17O + 1) – λRL ln(δ18O + 1)) analysis of small mass silicate and oxide materials. The analyses were conducted by laser fluorination in combination with gas chromatography and continuous flow isotope ratio monitoring gas spectrometry. We could analyze the oxygen isotope composition of samples down to 1 μg, which corresponded to about 13 nmol O2. The analytical error (we report the 1σ external reproducibility of a single analysis) in δ18O increases with decreasing sample sizes from ~0.2‰ for ~20 μg samples to ~0.9‰ for 1 μg samples. For Δ′17O, we achieved an external reproducibility of 0.04‰ for a sample mass range between 1 and 27 μg. The uncertainty in Δ′17O is smaller than the uncertainty in δ18O due to the correlated errors in δ17O and δ18O. We applied the method to urban micrometeorites, that is, small meteorites (<2 mm) that were sampled from a rooftop in Berlin, Germany. A total of 10 melted micrometeorites (S-type cosmic spherules, masses between 11 and 22 μg) were analyzed. The oxygen isotope compositions are comparable to that of modern Antarctic collections, indicating that the urban micrometeorites sample the same population. No indication for terrestrial weathering had been identified in the studied set of urban micrometeorites making them suitable materials for the study of micrometeorite origins.  相似文献   

6.
The bulk chlorine concentrations and isotopic compositions of a suite of non‐carbonaceous (NC) and carbonaceous (CC) iron meteorites were measured using gas source mass spectrometry. The δ37Cl values of magmatic irons range from ?7.2 to 18.0‰ versus standard mean ocean chloride and are unrelated to their chlorine concentrations, which range from 0.3 to 161 ppm. Nonmagmatic IAB irons are comparatively Cl‐rich containing >161 ppm with δ37Cl values ranging from ?6.1 to ?3.2‰. The anomalously high and low δ37Cl values are inconsistent with a terrestrial source, and as Cl contents in magmatic irons are largely consistent with derivation from a chondrite‐like silicate complement, we suggest that Cl is indigenous to iron meteorites. Two NC irons, Cape York and Gibeon, have high cooling rates with anomalously high δ37Cl values of 13.4 and 18.0‰. We interpret these high isotopic compositions to result from Cl degassing during the disruption of their parent bodies, consistent with their low volatile contents (Ga, Ge, Ag). As no relevant mechanisms in iron meteorite parent bodies are expected to decrease δ37Cl values, whereas volatilization is known to increase δ37Cl values by the preferential loss of light isotopes, we interpret the low isotope values of <?5‰ and down to ?7.2‰ to most closely represent the primordial isotopic composition of Cl in the solar nebula. Similar conclusions have been derived from low δ37Cl values down to ?6, and ?3.8‰ measured in Martian and Vestan meteorites, respectively. These low δ37Cl values are in contrast to those of chondrites which average around 0‰ previously explained by the incorporation of isotopically heavy HCl clathrate into chondrite parent bodies. The poor retention of low δ37Cl values in many differentiated planetary materials suggest that extensive devolatilization occurred during planet formation, which can explain Earth's high δ37Cl value by the loss of approximately 60% of the initial Cl content.  相似文献   

7.
Abstract Diamonds isolated from primitive chondrites of the carbonaceous, ordinary and enstatite groups have been analysed by high-resolution stepped combustion, followed by measurement of their C and N isotopes using a newly adapted technique that allows quantitative measurements of C/N ratios. The δ13C of the diamond is shown to vary between meteorite groups from ?32 to ?38%0, and the measured C/N ratios suggest that the N concentration of diamond ranges over a factor of 7 from 1800 ppm (Tieschitz) to 13,000 ppm (Adrar 003). The δ15N of N released from diamond is constrained to ?348 ± 7%. The complexity of the C release pattern and C/N ratio during combustion implies the presence of more than one component, which suggests that either more than one type of diamond is present in the samples, or unidentified additional phases are located in the acid-resistant residue. The components are present in varying proportions between meteorite groups. The data are compatible with a model of a mix of different diamond populations (some probably presolar and some possibly solar) existing in the early solar nebula, where each population originally contributed a roughly equal amount to chondrites of every class. Subsequent metamorphism has resulted in overall variations in δ13C and C/N ratios in diamond isolated from meteorites of differing petrologic grade without significantly altering the N isotopic composition. Possible ways for this to be achieved are explored.  相似文献   

8.
Abstract— We have studied the carbon and nitrogen stable isotope geochemistry of a small pristine sample of the Tagish Lake carbonaceous chondrite by high‐resolution stepped‐combustion mass spectrometry, and compared the results with data from the Orgueil (CI1), Elephant Moraine (EET) 83334 (CM1) and Murchison (CM2) chondrites. The small chip of Tagish Lake analysed herein had a higher carbon abundance (5.81 wt%) than any other chondrite, and a nitrogen content (?1220 ppm) between that of CI1 and CM2 chondrites. Owing to the heterogeneous nature of the meteorite, the measured carbon abundance might be artificially high: the carbon inventory and whole‐rock carbon isotopic composition (δ13C ? +24.4%o) of the chip was dominated by 13C‐enriched carbon from the decomposition of carbonates (between 1.29 and 2.69 wt%; δ13C ? +67%o and δ18O ? +35%o, in the proportions ?4:1 dolomite to calcite). In addition to carbonates, Tagish Lake contains organic carbon (?2.6 wt%, δ13C ? ?9%o; 1033 ppm N, δ15N ? +77%o), a level intermediate between CI and CM chondrites. Around 2% of the organic material is thermally labile and solvent soluble. A further ?18% of the organic species are liberated by acid hydrolysis. Tagish Lake also contains a complement of presolar grains. It has a higher nanodiamond abundance (approximately 3650–4330 ppm) than other carbonaceous chondrites, along with ?8 ppm silicon carbide. Whilst carbon and nitrogen isotope geochemistry is not diagnostic, the data are consistent with classification of Tagish Lake as a CI2 chondrite.  相似文献   

9.
Abstract— The N and C abundances and isotopic compositions of acid-insoluble carbonaceous material in thirteen primitive chondrites (five unequilibrated ordinary chondrites, three CM chondrites, three enstatite chondrites, a CI chondrite and a CR chondrite) have been measured by stepped combustion. While the range of C isotopic compositions observed is only ～δ13C = 30%, the N isotopes range from δ15N ' -40 to 260%. After correction for metamorphism, presolar nanodiamonds appear to have made up a fairly constant 3–4 wt% of the insoluble C in all the chondrites studied. The apparently similar initial presolar nanodiamond to organic C ratios, and the correlations of elemental and isotopic compositions with metamorphic indicators in the ordinary and enstatite chondrites, suggest that the chondrites all accreted similar organic material. This original material probably most closely resembles that now found in Renazzo and Semarkona. These two meteorites have almost M-shaped N isotope release profiles that can be explained most simply by the superposition of two components, one with a composition between δ15N = -20 and -40% and a narrow combustion interval, the other having a broader release profile and a composition of δ15N ～ 260%. Although isotopically more subdued, the CI and the three CM chondrites all appear to show vestiges of this M-shaped profile. How and where the components in the acid-insoluble organics formed remains poorly constrained. The small variation in nanodiamond to organic C ratio between the chondrite groups limits the local synthesis of organic matter in the various chondrite formation regions to at most 30%. The most 15N-rich material probably formed in the interstellar medium, and the fraction of organic N in Renazzo in this material ranges from 40 to 70%. The isotopically light component may have formed in the solar system, but the limited range in nanodiamond to total organic C ratios in the chondrite groups is consistent with most of the organic material being presolar.  相似文献   

10.
Abstract— We used the nuclear reaction 37Cl (n,γ) 38Ar, achieved during neutron irradiation for dating meteorites by the 39Ar‐40Ar technique, to calculate the elemental Cl concentration of 132 samples of 94 different meteorites (mostly finds) representing several different classes. determined k and ca concentrations are also reported. Total [Cl] varies considerably, both among meteorites of the same class and among different meteorite classes. The range in [Cl] is approximately 15–177 ppm for ordinary chondrites; approximately 24–650 ppm for enstatite chondrites; approximately 4–177 ppm for eucrites; approximately 7–128 ppm for mesosiderites; approximately 35–268 ppm for acapulcoites and lodranites; and approximately 12–507 ppm for winonaites and iron silicates. As expected, most differentiated meteorites have lower [Cl] compared to chondrites and iron silicates. Analyses of 11 interior samples (～0.1 g each) of a large L6 chondrite varied over 68–129 ppm, which is a measure of the homogeneity of Cl distribution. By evaluating Ar release during stepwise sample degassing, we separated the Cl into low‐temperature and high‐temperature components, the former of which may consist of terrestrial contamination. Most samples show low‐temperature Cl concentrations of <40 ppm, but for several samples terrestrial Cl contamination constitutes significant fractions of the total Cl. Among most differentiated meteorites, finds show considerably greater low‐temperature [Cl] compared to falls.  相似文献   

11.
We report on the investigation of presolar grain inventories of hydrated lithic clasts in three metal-rich carbonaceous chondrites from the CR clan, Acfer 182 (CH3), Isheyevo (CH3/CBb3), and Lewis Cliff (LEW) 85332 (C3-un), as well as the carbon- and nitrogen-isotopic compositions of the fine-grained clast material. Eleven presolar silicate grains as well as nine presolar silicon carbide (SiC) grains were identified in the clasts. Presolar silicate abundances range from 4 to 22 parts per million (ppm), significantly lower than in pristine meteorites and interplanetary dust particles (IDP), and comparable to recent findings for CM2s and CR2 interchondrule matrix. SiC concentrations lie between 9 and 23 ppm, and are comparable to the values for CI, CM, and CR chondrites. The results of our investigation suggest similar alteration pathways for the clast material, the interchondrule matrix of the CR2 chondrites, and the fine-grained fraction of CM2 chondrites. Fine-grained matter of all three meteorites contains moderate to high 15N-enrichments (~50‰ ≤ δ15N ≤ ~1600‰) compared to the terrestrial value, indicating the presence of primitive organic material. We observed no correlation between 15N-enrichments and presolar dust concentrations in the clasts. This is in contrast to the findings from a suite of primitive IDPs, which display in several cases enhanced bulk 15N/14N ratios and high presolar grain abundances of several hundred or even thousand ppm. The bulk 15N/14N ratios of the clasts are comparable to the range for primitive IDPs, suggesting a nitrogen carrier less susceptible to destruction by aqueous alteration than silicate stardust.  相似文献   

12.
Abstract– We have investigated the terrestrial ages, or residence times, of 78 meteorites (representing 73 discrete falls) recovered in Western Australia, and one from South Australia, using both 14C measurements and also 14C/10Be. The samples studied included two ureilites, one CK and one EL chondrite. We have included 10Be measurements from 30 meteorites, including some meteorites for which the 14C terrestrial age was previously determined. We find that the 14C/10Be terrestrial ages are more precise than 14C alone, as we can correct for shielding effects. In general, the two different age determinations age by 14C–10Be are precise to 0.5–1 ka and 14C alone within 1–2 ka. However, measurement of the 14C age alone gives good agreement with the 14C–10Be for most samples. The study of the terrestrial ages of meteorites gives us useful information concerning the storage and weathering of meteorites and the study of fall times and terrestrial age. We have compared the terrestrial ages to weathering, degree of oxidation (estimated from Mössbauer studies) and Δ17O. In this study, we found that weathering is not well correlated with terrestrial age for Nullarbor meteorites. However, there is a good correlation between degree of oxidation and Δ17O. The implications for the study of terrestrial ages and weathering from other desert environments will be discussed.  相似文献   

13.
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   

14.
Abstract— We report the discovery of presolar silicate, oxide (hibonite), and (possibly) SiC grains in four Antarctic micrometeorites (AMMs). The oxygen isotopic compositions of the eighteen presolar silicate (and one oxide) grains found are similar those observed previously in primitive meteorites and interplanetary dust particles, and indicate origins in oxygen‐rich red giant or asymptotic giant branch stars, or in supernovae. Four grains with anomalous C isotopic compositions were also detected. 12C/13C as well as Si ratios are similar to those of mainstream SiC grains; the N isotopic composition of one grain is also consistent with a mainstream SiC classification. Presolar silicate grains were found in three of the seven AMMs studied, and are heterogeneously distributed within these micrometeorites. Fourteen of the 18 presolar silicate grains and 3 of the 4 C‐anomalous grains were found within one AMM, T98G8. Presolar silicate‐bearing micrometeorites contain crystalline silicates that give sharp X‐ray diffractions and do not contain magnesiowüstite, which forms mainly through the decomposition of phyllosilicates and carbonates. The occurrence of this mineral in AMMs without presolar silicates suggests that secondary parent body processes probably determine the presence or absence of presolar silicates in Antarctic micrometeorites.  相似文献   

15.
Abstract— We have measured the 13C/12C and 14C/12C ratios in CO2 released by acid etching of the carbonate-bearing SNC meteorites Allan Hills 84001 and Nakhla. Most of the C released is strongly enriched in 13C. In 10 out of 12 samples, 15‰ <δ13C < 55‰. Terrestrial values of carbonateδ13C from weathering products are generally between ?10 and +10‰. Two leachate samples especially rich in 13C, ALH 84001,27 and Nakhla 25, have elemental Si/Mg ratios much lower than those of the bulk meteorites and 14C activities that are much lower than the values expected for terrestrial carbonates. The former observation indicates that these leachates consist primarily of carbonates and, less likely, phosphates. The latter observation implies that heavy C was introduced not by terrestrial weathering but by extraterrestrial processes. For ALH 84001,121 (sample 27) and Nakhla (BM 1913,26) δ13C = +41‰ and +35‰, respectively. The measured 18O/16O ratios in the leaches are similar: δ18O ～ 15 ± 5‰, contrasting with 4.2‰ in the bulk silicates. We infer that the C in the carbonates retains an extraterrestrial isotopic signature, but probably not O, due to its ease of isotopic exchange (Cole and Ohmoto, 1986).  相似文献   

16.
Abstract The 244Pu-fission-136Xe retention ages of howardites, eucrites, and diogenites (HEDs) show that these meteorites have retained Xe since they were formed about 4500 Ma ago. For the Garland diogenite and the Millbillillie eucrite, we obtain fission Xe ages of 4525 ± 40 Ma and 4486 ± 40 Ma, respectively. If Xe isotope data reported by other workers are also considered, we conclude that the monomict equilibrated eucrites Camel Donga, Juvinas, and Millbillillie formed about 40 Ma later than Pasamonte, a polymict unequilibrated eucrite. Stannern, a monomict equilibrated brecciated eucrite, yields a 244Pu-136Xe age of 4442 Ma. The 40K-40Ar retention ages fall, for most HEDs, into the 1000–4000 Ma age range, indicating that 40Ar is generally not well retained. The good retentivity for Xe of HEDs allows us to study primordial trapped Xe in these meteorites. Except for Shalka, in which other authors found Kr and Xe from terrestrial atmospheric contamination only, we present for the first time Kr and Xe isotopic data for diogenites. We studied Ellemeet, Garland, Ibbenbühren, Shalka, and Tatahouine. We show that Tatahouine contains two types of trapped Xe: a terrestrial contamination acquired by an irreversible adsorption process and released at pyrolysis temperatures up to 800 °C, and indigenous primordial Xe released primarily between 800 °C and 1200 °C. The isotopic composition of this primordial Xe is identical to that proposed earlier to be present in primitive achondrites and termed U-Xe or “primitive” Xe, but it has not been directly observed in achondrites until now. This type of primitive Xe is important for understanding the evolution of other Xe reservoirs in the Solar System. Terrestrial atmospheric Xe (corrected for fission Xe and radiogenic Xe from outgassing of the Earth) is related to it by a mass dependent fractionation favoring the heavier Xe isotopes. This primitive Xe is isotopically very similar to solar Xe except for 134Xe and 136Xe. Solar Xe appears to contain an enrichment of unknown origin for these isotopes relative to the primitive Xe.  相似文献   

17.
Abstract— The varied organic suite extracted from the Murchison meteorite contains several amino acids that are common to the biosphere. Some of these have been found to be non‐racemic, but the indigenous nature of their L‐enantiomeric excesses has been subject to debate in view of possible terrestrial contamination. We have investigated two amino acids of common terrestrial and meteoritic occurrence, alanine and glutamic acid, and assessed their indigenous enantiomeric ratios in the Murchison and Murray meteorites through the ratios of some of their derivatives. Analyzed were N‐acetyl alanine, α‐imino propioacetic acid, N‐acetyl glutamic acid and pyroglutamic acid. Both alanine derivatives were found to be racemic, while those of glutamic acid showed L‐enantiomeric excesses varying from 16% to 47.2% for pyroglutamic acid, and from 8.6% to 41% for N‐acetyl glutamic acid. The δ13C was determined for the two enantiomers of Murchison pyroglutamic acid both before and after acid hydrolysis to glutamic acid. The values of +27.7%0 (D‐pyro), +10.0%0 (L‐pyro), +32.2%0 (D‐glu) and +14.6%0 (L‐glu) were obtained. The racemic nature of alanine derivatives strongly suggests that alanine itself, as indigenous to the meteorite, is racemic. The explanation of the L‐enantiomeric excesses found for glutamic acid derivatives is less direct; however, the variability of the enantiomeric ratios for these compounds and the distinctly lower δ13C values determined for pyroglutamic L‐enantiomer point to a terrestrial contamination, possibly dating to the time of fall.  相似文献   

18.
Abstract— Ten glass cosmic spherules (CS) from the South Pole water well collection were analyzed by electron microprobe. Nine of them have Fe/Mn and Fe/Mg ratios in the range typical of chondrites. One of them (SP37‐3), along with up to six other previously analyzed CS, have nonchondritic Fe/Mn and Fe/Mg ratios that agree well with values typical of either (basaltic) howardite, eucrite, and diogenite (HED) meteorites or Martian basalts, but not of lunar samples. SP37‐3 also contains an anorthite relic grain. Anorthite has not previously been reported in cosmic spherules, but is well known in HED meteorites. The much greater frequency of HEDs among hand‐sized meteorites suggests but does not prove that HED precursors are more likely for the nonchondritic spherules. We estimate that HED‐like micrometeorites constitute ～0.5 ± 0.4% of the total population of micrometeorites in the South Pole water well, a fraction that translates to a flux of 1.6 ± 0.3 × 10?8g HED micrometeorites/m2‐y. The ratio of HED‐like objects to carbonaceous objects is about 100 times less in micrometeorites than among hand‐size specimens. We infer that the comparative mechanical weakness of carbonaceous precursor materials tends to encourage spherule formation.  相似文献   

19.
Abstract— Isotopic analysis of nesquehonite recovered from the surface of the LEW 85320 H5 ordinary chondrite shows that the δ13C and δ18O values of the two generations of bicarbonate (Antarctic and Texas) are different: δ13C = +7.9‰ and +4.2‰; δ18O = +17.9‰ and + 12.1‰ respectively. Carbon isotopic compositions are consistent with equilibrium formation from atmospheric carbon dioxide at ?2 ± 4 °C (Antarctic) and +16 ± 4 °C (Texas). Oxygen isotopic data imply that the water required for nesquehonite precipitation was derived from atmospheric water vapour or glacial meltwater which had locally exchanged with silicates, either in the meteorite or in underlying bedrock. Although carbonates with similar δ13C values have been identified in the SNC meteorites EETA 79001 and Nakhla, petrographic and temperature constraints argue against their simply being terrestrial weathering products.  相似文献   

20.
This study characterizes carbon and nitrogen abundances and isotopic compositions in ureilitic fragments of Almahata Sitta. Ureilites are carbon‐rich (containing up to 7 wt% C) and were formed early in solar system history, thus the origin of carbon in ureilites has significance for the origin of solar system carbon. These samples were collected soon after they fell, so they are among the freshest ureilite samples available and were analyzed using stepped combustion mass spectrometry. They contained 1.2–2.3 wt% carbon; most showed the major carbon release at temperatures of 600–700 °C with peak values of δ13C from ?7.3 to +0.4‰, similar to literature values for unbrecciated (“monomict”) ureilites. They also contained a minor low temperature (≤500 °C) component (δ13C = ca ?25‰). Bulk nitrogen contents (9.4–27 ppm) resemble those of unbrecciated ureilites, with major releases mostly occurring at 600–750 °C. A significant lower temperature release of nitrogen occurred in all samples. Main release δ15N values of ?53 to ?94‰ fall within the range reported for diamond separates and acid residues from ureilites, and identify an isotopically primordial nitrogen component. However, they differ from common polymict ureilites which are more nitrogen‐rich and isotopically heavier. Thus, although the parent asteroid 2008TC3 was undoubtedly a polymict ureilite breccia, this cannot be deduced from an isotopic study of individual ureilite fragments. The combined main release δ13C and δ15N values do not overlap the fields for carbonaceous or enstatite chondrites, suggesting that carbon in ureilites was not derived from these sources.  相似文献   

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