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1.
Abstract— We have the elemental abundances and isotopic compositions of noble gases in Muong Nong‐type tektites from the Australasian strewn field by crushing and by total fusion of the samples. We found that the abundances of the heavy noble gases are significantly enriched in Muong Nong‐type tektites compared to those in normal splash‐form tektites from the same strewn field. Neon enrichments were also observed in the Muong Nong‐type tektites, but the Ne/Ar ratios were lower than those in splash‐form tektites because of the higher Ar contents in the former. The absolute concentrations of the heavy noble gases in Muong Nong‐type tektites are similar to those in impact glasses. The isotopic ratios of the noble gases in Muong Nong‐type tektites are mostly identical to those in air, except for the presence of radiogenic 40Ar. The obtained K‐Ar ages for Muong Nong‐type tektites were about 0.7 Myr, similar to ages of other Australasian tektites. The crushing experiments suggest that the noble gases in the Muong Nong‐type tektites reside mostly in vesicles, although Xe was largely affected by adsorbed atmosphere after crushing. We used the partial pressure of the heavy noble gases in vesicles to estimate the barometric pressure in the vesicles of the Muong Nong‐type tektites. Likely, Muong Nong‐type tektites solidified at the altitude (between the surface and a maximum height of 8–30 km) lower than that for splash‐form tektites.  相似文献   

2.
Abstract— Elemental and isotopic compositions of the noble gases have been determined in six North American tektites (4 bediasites and 2 georgiaites) and one Ivory Coast tektite. Radiogenically produced 4He may explain the large 4He/36Ar ratios measured relative to air, despite significant diffusive losses. The Ne isotopic composition is enriched in 20Ne consistent with a single stage mass fractionation process. The enormous 20Ne/36Ar enrichments observed in all tektite samples, similar to those reported from other tektites and impact glasses, are attributed to atmospheric diffusion into the samples following solidification. The North American tektites show a systematic increase in 84Kr/36Ar and 132Xe/36Ar relative to air, with enrichments greater than those determined for any other tektite group or terrestrial samples other than shales. These enrichments are inconsistent with existing models of dissolving Kr and Xe in tektite glass without elemental fractionation at atmospheric pressures equivalent to ∼40 km altitude. The Kr and Xe isotopic compositions are indistinguishable from atmospheric within experimental uncertainty.  相似文献   

3.
Abstract— Three samples of Muong Nong tektites have been studied for N and noble gases. The isotopic composition of noble gases is airlike. The noble gas amounts are much higher in Muong Nong tektites than in splash-form tektites. As compared to air, He and Ne have been enriched, most likely due to inward diffuion from ambient air, subsequent to glass formation. Nitrogen contents range from 0.3 to 1.34 ppm, with a non-atmospheric δ15N ranging from 8 to 17%. The release pattern of δ15N clearly shows the presence of two N components. Higher N/36Ar values than those of air, together with positive δ15N, show that a major portion of N in Muong Nong tektites is a remnant from the sedimentary source material.  相似文献   

4.
Abstract Solar noble gases He, Ne, Ar and Kr implanted in the H3–6 meteorite regolith breccia Acfer 111 agree in their elemental composition with that in present-day solar wind and, except for a 25% deficit of 4He, also with adopted solar abundances. The presence of such unfractionated solar gases makes Acfer 111 unique (until now). Closed system stepped etching releases noble gases that can be explained as mixtures of two distinct types of He, Ne, and Kr of isotopic compositions as they have been derived previously from meteorites and lunar samples that contain heavily fractionated solar gases. Since the same putative end members, ascribed to the solar wind (SW) and supra-thermal solar energetic particles (SEP), are also present in Acfer 111, we argue that these end members represent two truly independent components. We discount the possibility that one isotopic composition derived from the other by diffusion of the gases within, or upon their release from, their host phases. The isotopic signatures of noble gases in Acfer 111 agree with those in a lunar ilmenite of young antiquity ?100 Ma) but are in disagreement with the noble gases in lunar ilmenite 79035 of 1–2 Ga antiquity. Systematic changes are discussed of the nuclide abundance ratios as etching proceeds; they are ascribed to differences in trapping efficiency and in penetration depth of the different noble gas ion species upon their implantation.  相似文献   

5.
Abstract— Abundances and isotopic compositions of noble gases in metal and graphite of the Bohumilitz IAB iron meteorite were measured. The abundance ratios of spallogenic components in metal reveal a 3He deficiency which is due to the diffusive loss of parent isotopes, that is, tritium (Tilles, 1963; Schultz, 1967). The diffusive loss likely has been induced by thermal heating by the Sun during cosmic‐ray exposure (～160 Ma; Lavielle et al, 1999). Thermal process such as impact‐induced partial loss may have affected the isotopic composition of spallogenic Ne. The 129Xe/131Xe ratio of cosmogenic components in the metal indicates an enhanced production of epi‐thermal neutrons. The abundance ratios of spallogenic components in the graphite reveal that it contained small amounts of metal and silicates. The isotopic composition of heavy noble gases in graphite itself was obtained from graphite treated with HF/HCl. The isotopic composition of the etched graphite shows that it contains two types of primordial Xe (i.e., Q‐Xe and El Taco Xe). The isotopic heterogeneity preserved in the Bohumilitz graphite indicates that the Bohumilitz graphite did not experience any high‐temperature event and, consequently, must have been emplaced into the metal at subsolidus temperatures. This situation is incompatible with an igneous model as well as the impact melting models for the IAB‐IIICD iron meteorites as proposed by Choi et al. (1995) and Wasson et al (1980).  相似文献   

6.
Abstract— The HF/HCI‐resistant residues of the chondrites CM2 Cold Bokkeveld, CV3 (ox.) Grosnaja, CO3.4 Lancé, CO3.7 Isna, LL3.4 Chainpur, and H3.7 Dimmitt have been measured by closed‐system stepped etching (CSSE) in order to better characterise the noble gases in “phase Q”, a major carrier of primordial noble gases. All isotopic ratios in phase Q of the different meteorites are quite uniform, except for (20Ne/22Ne)Q. As already suggested by precise earlier measurements (Schelhaas et al., 1990; Wieler et al., 1991, 1992), (20Ne/22Ne)Q is the least uniform isotopic ratio of the Q noble gases. The data cluster ～10.1 for Cold Bokkeveld and Lancé and 10.7 for Chainpur, Grosnaja, and Dimmitt, respectively. No correlation of (20Ne/22Ne)Q with the classification or the alteration history of the meteorites has been found. The Ar, Kr, and Xe isotopic ratios for all six samples are identical within their uncertainties and similar to earlier Q determinations as well as to Ar‐Xe in ureilites. Thus, an unknown process probably accounts for the alteration of the originally incorporated Ne‐Q. The noble gas elemental compositions provide evidence that Q consists of at least two carbonaceous carrier phases “Q1” and “Q2” with slightly distinct chemical properties. Ratios (Ar/Xe)Q and (Kr/Xe)Q reflect both thermal metamorphism and aqueous alteration. These parent‐body processes have led to larger depletions of Ar and Kr relative to Xe. In contrast, meteorites that suffered severe aqueous alteration, such as the CM chondrites, do not show depletions of He and Ne relative to Ar but rather the highest (He/Ar)Q and (Ne/Ar)Q ratios. This suggests that Q1 is less susceptible to aqueous alteration than Q2. Both subphases may well have incorporated noble gases from the same reservoir, as indicated by the nearly constant, though very large, depletion of the lighter noble gases relative to solar abundances. However, the elemental ratios show that Q1 and Q2 must have acquired (or lost) noble gases in slightly different element proportions. Cold Bokkeveld suggests that Q1 may be related to presolar graphite. Phases Q1 and Q2 might be related to the subphases that have been suggested by Gros and Anders (1977). The distribution of the 20Ne/22Ne ratios cannot be attributed to the carriers Q1 and Q2. The residues of Chainpur and Cold Bokkeveld contain significant amounts of Ne‐E(L), and the data confirm the suggestion of Huss (1997) that the 22Ne‐E(L) content, and thus the presolar graphite abundances, are correlated with the metamorphic history of the meteorites.  相似文献   

7.
Abstract— Noble gases in two ureilites, Kenna and Allan Hills (ALH) 78019, were measured with two extraction methods: mechanical crushing in a vacuum and heating. Large amounts of noble gases were released by crushing, up to 26.5% of 132Xe from ALH 78019 relative to the bulk concentration. Isotopic ratios of the crush‐released Ne of ALH 78019 resemble those of the trapped Ne components determined for some ureilites or terrestrial atmosphere, while the crush‐released He and Ne from Kenna are mostly cosmogenic. The crush‐released Xe of ALH 78019 and Kenna is similar in isotopic composition to Q gas, which indicates that the crush‐released noble gases are indigenous and not caused by contamination from terrestrial atmosphere. In contrast to the similarities in isotopic composition with the bulk samples, light elements in the crush‐released noble gases are depleted relative to Xe and distinct from those of each bulk sample. This depletion is prominent especially in the 20Ne/132Xe ratio of ALH 78019 and the 36Ar/132Xe ratio of Kenna. The values of measured 3He/21Ne for the gases released by crushing are significantly higher than those for heating‐released gases. This suggests that host phases of the crush‐released gases might be carbonaceous because cosmogenic Ne is produced mainly from elements with a mass number larger than Ne. Based on our optical microscopic observation, tabular‐foliated graphite is the major carbon mineral in ALH 78019, while Kenna contains abundant polycrystalline graphite aggregates and diamonds along with minor foliated graphite. There are many inclusions at the edge and within the interior of olivine grains that are reduced by carbonaceous material. Gaps can be seen at the boundary between carbonaceous material and silicates. Considering these petrologic and noble gas features, we infer that possible host phases of crush‐released noble gases are graphite, inclusions in reduction rims, and gaps between carbonaceous materials and silicates. The elemental ratios of noble gases released by crushing can be explained by fractionation, assuming that the starting noble gas composition is the same as that of amorphous carbon in ALH 78019. The crush‐released noble gases are the minor part of trapped noble gases in ureilites but could be an important clue to the thermal history of the ureilite parent body. Further investigation is needed to identify the host phases of the crush‐released noble gases.  相似文献   

8.
The isotopic compositions of noble gases in the solar wind show high enrichments of light isotopes. When corrected for mass fractionation all five noble gases there can be resolved in terms of the two primitive noble gas components that have been identified in planetary solids. Reasons are presented for assigning the fractionation to a solar process that selectively enriches lighter nuclei at the surface of the Sun. When abundances of the elements at the Sun's surface are corrected for this fractionation, it is shown that atomic abundances for major elements in the bulk Sun are (in decreasing order): Fe, Ni, O, Si, S and Mg. Solar elements at about the 1% atomic abundance level include He, C, Ne, Ca and Cr. These results suggest that fusion of hydrogen is probably not the Sun's primary energy source.  相似文献   

9.
Abstract— We measured abundances and isotopic compositions of noble gases in metal and schreibersite of the Acuña (IIIAB) iron meteorite. The concentrations of noble gases in Acuña metal are very low compared to those reported so far for other iron meteorites. The isotopic ratios of He, Ne and Ar indicate that they are mostly of cosmogenic origin. Cosmogenic components are even present in Kr and Xe, which could not have been produced from Fe, Ni and P and are probably due to the spallation of trace elements of higher masses. The high 4He/21Ne ratio of 420 in Acuña metal indicates that the samples were at a deep position within a very large meteoroid. The exposure ages of Acuña were estimated to be 50–200 Ma from 3He, 21Ne and 38Ar abundances and by utilizing the diagrams of production rates vs. the 4He/21Ne ratio based on the Signer-Nier model. The low exposure age of Acuña may indicate a history different from that of other IIIAB irons whose exposure ages cluster at ～670 Ma. Otherwise, Acuña may be one of the samples with the low production rate, which can not be estimated from the diagrams of the Signer-Nier model.  相似文献   

10.
Abstract– We have determined the elemental abundances and the isotopic compositions of noble gases in a bulk sample and an HF/HCl residue of the Saratov (L4) chondrite using stepwise heating. The Ar, Kr, and Xe concentrations in the HF/HCl residue are two orders of magnitude higher than those in the bulk sample, while He and Ne concentrations from both are comparable. The residue contains only a portion of the trapped heavy noble gases in Saratov; 40 ± 9% for 36Ar, 58 ± 12% for 84Kr, and 48 ± 10% for 132Xe, respectively. The heavy noble gas elemental pattern in the dissolved fraction is similar to that in the residue but has high release temperatures. Xenon isotopic ratios of the HF/HCl residue indicate that there is no Xe‐HL in Saratov, but Ne isotopic ratios in the HF/HCl residue lie on a straight line connecting the cosmogenic component and a composition between Ne‐Q and Ne‐HL. This implies that the Ne isotopic composition of Q has been changed by incorporating Ne‐HL (Huss et al. 1996) or by being mass fractionated during the thermal metamorphism. However, it is most likely that the Ne‐Q in Saratov is intrinsically different from this component in other meteorites. The evidence of this is a lack of correlation between the isotopic ratio of Ne‐Q and petrologic types of meteorites (Busemann et al. 2000). A neutron capture effect was observed in the Kr isotopes, and this process also affected the 128Xe/132Xe ratio. The 3He and 21Ne exposure ages for the bulk sample are 33 and 35 Ma, respectively.  相似文献   

11.
Abstract— Five indochinites from Hainan Island and the Leizhou Peninsula, China were analyzed for noble gas abundances and isotopic ratios. These splash‐form tektites show vesiculation ranging from 0.4 vol% to 8 vol%, as determined by digital image analysis (software SXM®) on thin section photographs. To study the distribution of noble gases in vesicles and in glass, the gases were extracted by heating and by crushing, respectively, on 2 aliquots of the same sample. The results show that 5 to 53% of the total measured 20Ne resides in vesicles. The calculated concentration of neon dissolved in the glass is higher (0.7‐1 times 10?7 cm3STP/g) than that expected from solubility equilibrium (1 times 10?8 cm3STP/g), assuming solubility data from MORB glasses. The neon concentration of splash‐form tektites, those analyzed in this work and those from other strewn‐fields worldwide, is correlated with the SiO2 content of glass and with the nonbridging oxygen per tetrahedral cation in the melt (hereafter NBO/T ratio), the latter being an index of the free‐volume in the silica network where neon could be dissolved. These correlations suggest that the glass structure of tektite has a larger free‐volume available for dissolving noble gases than MORB glasses.  相似文献   

12.
Abstract— High-purity separates of presolar diamond were prepared from 14 primitive chondrites from 7 compositional groups. Their noble gases were measured using stepped pyrolysis. Three distinct noble gas components are present in diamonds, HL, P3, and P6, each of which is found to consist of five noble gases. P3 , released between 200 °C and 900 °C, has a “planetary” elemental abundance pattern and roughly “normal” isotopic ratios. HL , consisting of isotopically anomalous Xe-HL and Kr-H, Ar with high 38Ar/36Ar, and most of the gas making up Ne-A2 and He-A, is released between 1100 °C and 1600 °C. HL has “planetary” elemental ratios, except that it has much more He and Ne than other known “planetary” components. HL gases are carried in the bulk diamonds, not in some trace phase. P6 has a slightly higher median release temperature than HL and is not cleanly separated from HL by stepped pyrolysis. Our data suggest that P6 has roughly “normal” isotopic compositions and “planetary” elemental ratios. Both P3 and P6 seem to be isotopically distinct from P1, the dominant “planetary” noble-gas component in primitive chondrites. Release characteristics suggest that HL and P6 are sited in different carriers within the diamond fractions, while P3 may be sited near the surfaces of the diamonds. We find no evidence of separability of Xe-H and Xe-L or other isotopic variations in the HL component. However, because ～1010 diamonds are required to measure a Xe composition, a lack of isotopic variability does not constrain diamonds to come from a single source. In fact, the high abundance of diamonds in primitive chondrites and the presence of at least three distinct noble-gas components strongly suggest that diamonds originated in many sources. Relative abundances of noble-gas components in diamonds correlate with degree of thermal processing (see companion paper), indicating that all meteorites sampled essentially the same mixture of diamonds. That mixture was probably inherited from the Sun's parent molecular cloud.  相似文献   

13.
The Genesis Discovery mission returned solar matter in the form of the solar wind with the goal of obtaining precise solar isotopic abundances (for the first time) and greatly improved elemental abundances. Measurements of the light noble gases in regime samples demonstrate that isotopes are fractionated in the solar wind relative to the solar photosphere. Theory is required for correction. Measurement of the solar wind O and N isotopes shows that these are very different from any inner solar system materials. The solar O isotopic composition is consistent with photochemical self‐shielding. For unknown reasons, the solar N isotopic composition is much lighter than essentially all other known solar system materials, except the atmosphere of Jupiter. Ne depth profiling on Genesis materials has demonstrated that Ne isotopic variations in lunar samples are due to isotopic fractionation during implantation without appealing to higher energy solar particles. Genesis provides a precise measurement of the isotopic differences of Ar between the solar wind and the terrestrial atmosphere. The Genesis isotopic compositions of Kr and Xe agree with data from lunar ilmenite separates, showing that lunar processes have not affected the ilmenite data and that solar wind composition has not changed on 100 Ma time scales. Relative to Genesis solar wind, ArKrXe in Q (the chondrite noble gas carrier) and the terrestrial atmosphere show relatively large light isotope depletions.  相似文献   

14.
Abstract– Noble gas isotopic compositions were measured for a eucritic pebble and bulk material of a silicate–metal mixture from the Vaca Muerta mesosiderite as well as pyroxene and plagioclase separated from the eucritic pebble by total melting and stepwise heating methods. Trapped noble gases were degassed completely by a high‐temperature thermal event, probably at the formation of the Vaca Muerta parent body (VMPB). The presence of fissiogenic Xe isotopes from extinct 244Pu in the bulk samples might be a result of rapid cooling from an early high‐temperature metamorphism. High concentrations of cosmogenic noble gases enabled us to determine precise isotopic ratios of cosmogenic Kr and Xe. Spallogenic Ne from Na and unique Ar isotopic compositions were observed. The 81Kr‐Kr exposure age of 168 ± 8 Myr for the silicate pebble is distinctly longer than the age of 139 ± 8 Myr for the bulk samples. The precursor of the pebble had been irradiated on the surface of the VMPB for more than 60 Myr (first stage irradiation), with subsequent incorporation into bulk materials approximately 4 Gyr ago. The Vaca Muerta meteorite was excavated from the VMPB 140 Myr ago (second stage irradiation). Relative diffusion rates among the cosmogenic Ar, Kr, and Xe based on data obtained by stepwise heating indicate that Kr and Xe can be partially retained in pyroxene and plagioclase under the condition that resets the K‐Ar system. This result supports the presence of fission Xe and of excess concentration of cosmogenic Kr, which could have survived the thermal event approximately 3.8 Gyr ago.  相似文献   

15.
Abstract— From November 1998 to January 1999, the 39th Japanese Antarctic Research Expedition (JARE) conducted a large‐scale micrometeorite collection at 3 areas in the meteorite ice field around the Yamato Mountains, Antarctica. The Antarctic micrometeorites (AMMs) collected were ancient cosmic dust particles. This is in contrast with the Dome Fuji AMMs, which were collected previously from fresh snows in 1996 and 1997 and which represent modern micrometeorites. To determine the noble gas concentrations and isotopic compositions of individual AMMs, noble gas analyses were carried out using laser‐gas extraction for 35 unmelted Yamato Mountains AMMs and 3 cosmic spherules. X‐ray diffraction analyses were performed on 13 AMMs before the noble gas measurement and mineral compositions were determined. AMMs are classified into 4 main mineralogical groups, defined from the heating they suffered during atmospheric entry. Heating temperatures of AMMs, inferred from their mineral compositions, are correlated with 4He concentrations and reflect the effect of degassing during atmospheric entry. Jarosite, an aqueous alteration product, is detected for 4 AMMs, indicating the aqueous alteration during long‐time storage in Antarctic ice. Jarosite‐bearing AMMs have relatively low concentrations of 4He, which is suggestive of loss during the alteration. High 3He/4He ratios are detected for AMMs with high 20Ne/4He ratios, showing both cosmogenic 3He and preferential He loss. SEP (solar energetic particles)‐He and Ne, rather than the solar wind (SW), were dominant in AMMs, presumably showing a preferential removal of the more shallowly implanted SW by atmospheric entry heating. The mean 20Ne/22Ne ratio is 11.27 ± 0.35, which is close to the SEP value of 11.2. Cosmogenic 21Ne is not detected in any of the particles, which is probably due to the short cosmic ray exposure ages. Ar isotopic compositions are explained by 3‐component mixing of air, Q, and SEP‐Ar. Ar isotopic compositions can not be explained without significant contributions of Q‐Ar. SEP‐Ne contributed more than 99% of the total Ne. As for 36Ar and 38Ar, the abundance of the Q component is comparable to that of the SEP component. 84Kr and 132Xe are dominated by the primordial component, and solar‐derived Xe is almost negligible.  相似文献   

16.
Abstract— We measured the noble gas isotopic abundances in lunar meteorite QUE 94269 and in bulk-, glass-, and crystal-phases of lunar meteorite QUE 94281. Our results confirm that QUE 94269 originated from the same meteorite fall as QUE 93069: both specimens yield the same signature of solar-particle irradiation and also the cosmogenic noble gases are in agreement within their uncertainities. Queen Alexandra Range 93069/94269 was exposed to cosmic rays in the lunar regolith for ～1000 Ma, and it trapped 3.5 × 10?4 cm3STP/g solar 36Ar, the other solar noble gases being present in proportions typical for the solar-particle irradiation. The bulk material of QUE 94281 contains about three times less cosmogenic and trapped noble gases than QUE 93069/94269 and the lunar regolith residence time corresponds to 400 ± 60 Ma. We show that in lunar meteorites the trapped solar 20Ne/22Ne ratio is correlated with the trapped ratio 40Ar/36Ar, that is, trapped 20Ne/22Ne may also serve as an antiquity indicator. The upper limits of the breccia compaction ages, as derived from the trapped ratio 40Ar/36Ar for QUE 93069/94269 and QUE 94281 are ～400 Ma and 800 Ma, respectively. We found very different regolith histories for the glass phase and the crystals separated from QUE 94281. The glass phase contains much less cosmogenic and solar noble gases than the crystals, in contrast to the glasses of lunar meteorite EET 87521, that were enriched in noble gases relative to the crystalline material. The QUE 94281 phases yield a 40K-40Ar gas retention age of 3770 Ma, which is in the range of that for lunar mare rocks.  相似文献   

17.
Abstract— A philippinite with a large bubble (volume ?5 cm3) was crushed in a specifically constructed device under vacuum. The total pressure, the major gas components, and the concentration and the isotopic composition of noble gases in the trapped gas were measured. The total gas pressure was found to be low, ～10?4 atm. Compared to terrestrial atmosphere, the abundances of He and Ne are considerably more enriched than the concentrations of the heavy noble gases. Unusually high 20Ne/22Ne and 21Ne/22Ne ratios were measured in the bubble gas. These ratios are higher than values expected for any steady state process and are interpreted to reflect very fast nonsteady state diffusion in the early stages of tektite formation.  相似文献   

18.
Abstract— We present Ne data from plagioclase separates from the solar noble‐gas‐rich meteorite Kapoeta, obtained mainly by in vacuo etching. samples rich in solar gases contain an excess of cosmogenic ne compared to solar‐gas‐poor samples, testifying to an exposure to cosmic rays in the parent body regolith. The 21Ne/22Ne ratio of the excess component is slightly lower than that of the Ne acquired during the meteoroid flight. Model calculations indicate that the observed isotopic composition of the excess Ne can be produced by galactic cosmic rays at a reasonable mean shielding of around a hundred to a few hundred grams per square centimeter. No substantial contribution from Ne produced by solar cosmic rays is needed to explain the data. We therefore conclude that they do not offer evidence for a substantially enhanced flux of solar energetic particles early in solar history, contrary to other claims. This conclusion is in agreement with solar flare track data.  相似文献   

19.
Abstract Noble gases and N were analyzed in handpicked metal separates from lunar soil 68501 by a combination of step-wise combustions and pyrolyses. Helium and Ne were found to be unfractionated with respect to one another when normalized to solar abundances, for both the bulk sample and for all but the highest temperature steps. However, they are depleted relative to Ar, Kr and Xe by at least a factor of 5. The heavier gases exhibit mass-dependent fractionation relative to solar system abundance ratios but appear unfractionated, both in the bulk metal and in early temperature steps, when compared to relative abundances derived from lunar ilmenite 71501 by chemical etching, recently put forward as representing the abundance ratios in solar wind. Estimates of the contribution of solar energetic particles (SEP) to the originally implanted solar gases, derived from a basic interpretation of He and Ne isotopes, yield values of about 10%. Analysis of the Ar isotopes requires a minimum of 20% SEP, and Kr isotopes, using our preferred composition for solar wind Kr, yield a result that overlaps both of these values. It is possible to reconcile the data from these gases if significant loss of solar wind Ar, Kr and presumably Xe has occurred relative to the SEP component, most likely by erosive processes that are mass independent, although mass-dependent losses (Ar > Kr > Xe) cannot be excluded. If such losses did occur, the SEP contribution to the solar implanted gases must have been no more than a few percent. Nitrogen is a mixture of indigenous meteoritic N, whose isotopic composition is inferred to be relatively light, and implanted solar N, which has probably undergone diffusive redistribution and fractionation. If the heavy noble gases have not undergone diffusive loss, then N/Ar in the solar wind can be inferred to be at least several times the accepted solar ratio. The solar wind N appears, even after correction for fractionation effects, to have a minimum δ15N value ≥+150‰ and a more probable value ≥+200‰.  相似文献   

20.
Effects of aqueous alteration on primordial noble gas carriers were investigated by analyzing noble gases and determining presolar SiC abundances in insoluble organic matter (IOM) from four Tagish Lake meteorite (C2‐ung.) samples that experienced different degrees of aqueous alteration. The samples contained a mixture of primordial noble gases from phase Q and presolar nanodiamonds (HL, P3), SiC (Ne‐E[H]), and graphite (Ne‐E[L]). The second most altered sample (11i) had a ~2–3 times higher Ne‐E concentration than the other samples. The presolar SiC abundances in the samples were determined from NanoSIMS ion images and 11i had a SiC abundance twice that of the other samples. The heterogeneous distribution of SiC grains could be inherited from heterogeneous accretion or parent body alteration could have redistributed SiC grains. Closed system step etching (CSSE) was used to study noble gases in HNO3‐susceptible phases in the most and least altered samples. All Ne‐E carried by presolar SiC grains in the most altered sample was released during CSSE, while only a fraction of the Ne‐E was released from the least altered sample. This increased susceptibility to HNO3 likely represents a step toward degassing. Presolar graphite appears to have been partially degassed during aqueous alteration. Differences in the 4He/36Ar and 20Ne/36Ar ratios in gases released during CSSE could be due to gas release from presolar nanodiamonds, with more He and Ne being released in the more aqueously altered sample. Aqueous alteration changes the properties of presolar grains so that they react similar to phase Q in the laboratory, thereby altering the perceived composition of Q.  相似文献   

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