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1.
Abstract— Isotopic variations have been reported for many elements in iron meteorites, with distinct N signatures found in the metal and graphite of IAB irons. In this study, a dozen IAB/IIICD iron meteorites (see Table 1 for new classifications) were analyzed by stepwise pyrolysis to resolve nitrogen components. Although isotopic heterogeneity has been presumed to be lost in thermally processed parent objects, the high‐resolution nitrogen isotopic data indicate otherwise. At least one reservoir has a light nitrogen signature, δ15N = ?(74 ± 2)‰, at 900 °C to 1000 °C, with a possible second, even lighter, reservoir in Copiapo (δ15N ≤ ?82‰). These releases are consistent with metal nitride decomposition or low‐temperature metal phase changes. Heavier nitrogen reservoirs are observed in steps ≤700 °C and at 1200 °C to 1400 °C. The latter release has a δ15N signature with a limit of ≥?16‰. Xenon isotopic signatures are sensitive indicators for the presence of inclusions because of the very low abundances of Xe in metal. The combined high‐temperature release shows 131Xe and 129Xe excesses to be consistent with shifts expected for Te(n,γ) reaction in troilite by epithermal neutrons, but there are also possible alterations in the isotopic ratios likely due to extinct 129I and cosmic‐ray spallation. The IAB/IIICD iron data imply that at least one light N component survived the formation processes of iron parent objects which only partially exchanged nitrogen between phases. Preservation of separate N reservoirs conflicts with neither the model of impact‐heating effects for these meteorites nor reported age differences between metal and silicates.  相似文献   

2.
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   

3.
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   

4.
Abstract— Nitrogen and noble gases were measured in a bulk sample and in acid‐resistant carbon‐rich residues of the ureilite Allan Hills (ALH) 78019 which has experienced low shock and is free of diamond. A small amount of amorphous carbon combusting at ≤500 °C carries most of the noble gases, while the major carbon phase consisting of large crystals of graphite combusts at ≥800 °C, and is almost noble‐gas free. Nitrogen on the other hand is present in both amorphous carbon and graphite, with different δ15N signatures of ?21%o and +19%o, respectively, distinctly different from the very light nitrogen (about ?100%o) of ureilite diamond. Amorphous carbon in ALH 78019 behaves similar to phase Q of chondrites with respect to noble gas release pattern, behavior towards oxidizing acids as well as nitrogen isotopic composition. In situ conversion of amorphous carbon or graphite to diamond through shock would require an isotopic fractionation of 8 to 12% for nitrogen favoring the light isotope, an unlikely proposition, posing a severe problem for the widely accepted shock origin of ureilite diamond.  相似文献   

5.
We report new data from Pesyanoe‐90,1 (dark lithology) on the isotopic signature of solar wind (SW) Xe as recorded in this enstatite achondrite which represents a soil‐breccia of an asteroidal regolith. The low temperature (≤800°C) steps define the Pesyanoe‐S xenon component, which is isotopically consistent with SW Xe reported for the lunar regolith. This implies that the SW Xe isotopic signature was the same at two distinct solar system locations and, importantly, also at different times of solar irradiation. Further, we compare the calculated average solar wind “SW‐Xe” signature to Chass‐S Xe, the indigenous Xe observed in SNC (Mars) meteorites. Again, a close agreement between these compositions is observed, which implies that a mass‐dependent differential fractionation of Xe between SW‐Xe and Chass‐S Xe is >1.5%o per amu. We also observe fractionated (Pesyanoe‐F) Xe and Ar components in higher temperature steps and we document a fission component due to extinct 244Pu. Interestingly, the Pesyanoe‐F Xe component is revealed only at the highest temperatures (>1200°C). The Pesyanoe‐F gas reveals Xe isotopic signatures that are consistent with lunar solar energetic particles (SEP) data and may indicate a distinct solar energetic particle radiation as was inferred for the moon. However, we cannot rule out fractionation processes due to parent body processes. We note that ratios 36Ar/38Ar≤5 are also consistent with SEP data. Calculated abundances of the fission component correlate well with radiogenic 40Ar concentrations, revealing rather constant 244Pu/K ratios in Pesyanoe, and separates thereof, and indicate that both components were retained. We identify a nitrogen component (δ15N = 44%o) of non‐solar origin with an isotopic signature distinct from indigenous N (δ15N = ?33%o). While large excesses at 128Xe and 129Xe are observed in the lunar regolith samples, these excesses in Pesyanoe are small. On the other hand, significant 126Xe isotopic excesses, comparable to relative excesses observed in lunar soils and breccias, are prominent in the intermediate temperature steps of Pesyanoe‐90,1.  相似文献   

6.
The present study has shown that the dependence of the isotopic composition of nitrogen on the N/C ratio, revealed from the data for bulk samples of meteoritic nanodiamond, can be obtained within the framework of the following model of the composition of populations of nanodiamond grains: (a) initial nanodiamond, i.e., the nanodiamond in the protoplanetary cloud before the accretion of the meteorite parent bodies, was composed mainly of grains of two populations (denoted as CN and CF), the ratio of which changed in meteorites depending on the degree of hydrothermal metamorphism; (b) only the grains of one of these populations (CN) contain volume-bound nitrogen with δ15N = ?350‰; (c) the grains of both populations contain surface-bound nitrogen (δ15N ≡ 0). The calculations revealed the following properties of population grains in this model. (1) The grains of the CN and CF populations are most likely the same in isotopic composition of carbon and heterogeneous in distribution of its isotopes: the central part of grains is enriched with the δ12C isotope relative to the remainder of the grain. While the value of δ13C is ?37.3 ± 1.1‰ for carbon in the central part, it is ?32.8 ± 1.5‰ for the whole volume of the grains. (2) The noble gases of the HL component, specifically Xe-HL, are anomalous in isotopic composition and are most likely contained in the third population of nanodiamond grains (denoted as CHL), the mass fraction of which is negligible relative to that for other grain populations. Only the grains of the CHL population have an undoubtedly presolar origin, while the grains of the other nanodiamond populations could have formed at the early stages of the evolution of the protoplanetary cloud material before the accretion of the meteoritic parent bodies.  相似文献   

7.
Angrites are a small group of ancient basaltic achondrites, notable for their unusual chemistry and extreme volatile depletion. No comprehensive study of indigenous light elements currently exists for the group. Measurement of the abundances and isotopic composition of carbon and nitrogen could provide information pertaining to the evolution of the angrite parent body. Bulk‐sample stepped combustion analyses of five angrites and a glass separate from D'Orbigny were combined with earlier data and acid dissolution experiments of carbonates found in D'Orbigny to compile an inventory of indigenous carbon and nitrogen. Indigenous carbon combusted between 700 °C and 1200 °C, with abundances of 10–140 ppm and a mass‐weighted δ13C of ?25 to ?20‰ with the exception of D'Orbigny (δ13C approximately ?5‰). Nitrogen was released at 850–1200 ºC, 1–20 ppm with a δ15N ?3‰ to +4‰; again, D'Orbigny (δ15N approximately +20 to +25‰) was an exception. We interpret these components as largely indigenous and decoupled; the carbon in graphitic or amorphous form, while the nitrogen is present as a dissolved component in the silicates. No relationship with the textural sub‐classification of angrites is apparent. We suggest that the angrite parent body contains a reservoir of reduced carbon and thus may have undergone a change in redox conditions, although the timing and mechanism for this remain unclear.  相似文献   

8.
We report new nitrogen and argon isotope and abundance results for single breccia clasts and agglutinates from four different sections of the Luna 24 drill core in order to re-evaluate the provenance of N trapped in lunar regolith, and to place limits on the flux of planetary material to the Moon’s surface. Single Luna 24 grains with 40Ar/36Ar ratios <1 show δ15N values between ?54.5‰ and +123.3‰ relative to terrestrial atmosphere. Thus, low-antiquity lunar soils record both positive and negative δ15N signatures, and the secular increase of the δ15N value previously postulated by Kerridge (Kerridge, J.F. [1975]. Science 188(4184), 162–164. doi:10.1126/science.188.4184.162) is no longer apparent when the Luna and Apollo data are combined. Instead, the N isotope signatures, corrected for cosmogenic 15N, are consistent with binary mixing between isotopically light solar wind (SW) N and a planetary N component with a δ15N value of +100‰ to +160‰. The lower δ15N values of Luna 24 grains compared to Apollo samples reflect a higher relative proportion of solar N, resulting from the higher SW fluence in the region of Mare Crisium compared to the central near side of the Moon. Carbonaceous chondrite-like micro-impactors match well the required isotope characteristics of the non-solar N component trapped in low-antiquity lunar regolith. In contrast, a possible cometary contribution to the non-solar N flux is constrained to be ?3–13%. Based on the mixing ratio of SW to planetary N obtained for recently exposed lunar soils, we estimate the flux of micro-impactors to be (2.2–5.7) × 103 tons yr?1 at the surface of the Moon. Our estimate for Luna 24 agrees well with that for young Apollo regolith, indicating that the supply of planetary material does not depend on lunar location. Thus, the continuous influx of water-bearing cosmic dust may have represented an important source of water for the lunar surface over the past ～1 Ga, provided that water removal rates (i.e., by meteorite impacts, photodissociation, and sputtering) do not exceed accumulation rates.  相似文献   

9.
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   

10.
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   

11.
Abstract— Nitrogen and noble gas isotopic compositions and C abundance of ureilites were analyzed using a stepwise combustion technique. Four Antarctic ureilites, ALHA77257, Asuka 881931, Yamato 791538 and Yamato 790981 were analyzed. Multiple N isotopic components were observed in these ureilites. The δ15N values of these N components ranged from +160 to ?120%. The minimum δ15N values of typically ?120% were observed at combustion temperatures at 700–900 °C where large amounts of C were released. A heavy N component was observed in only two ureilites, ALHA77257 and Asuka 881931. Silicate-enriched fractions and C-concentrated fractions were prepared for these two ureilites. We conclude that both the light N and the heavy N are trapped in the carbonaceous vein minerals. The lack of correction between the N/C ratio and the 36Ar/C ratio suggests that the primary carrier phase of the light N does not correspond to that of the planetary noble gases. We consider that the isotopically heavy N, which was observed in this study, is related to the heavy N observed among polymict ureilites. Small amounts (<0.5 ppm) of light N with the minimum δ15N value of ?120% were observed among the silicate fractions at the highest combustion temperature of 1200 °C, although the exact carrier phase of this light N is not known. We consider that the currently observed ureilites were produced by injection of several volatile-rich objects into volatile-poor ureilitic silicates.  相似文献   

12.
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   

13.
Abstract— Nitrogen abundances and isotopic compositions of four CK chondrites (ALH85002, EET92002, Yamato6903 and Karoonda) were measured by a stepped-combustion method. Neon and Ar were also measured for the same samples. Two types of isotopically light N were observed. One of them is labile N released at low temperatures (～300 °C). This N is observed only in ALH85002. The other N is extracted at high temperatures (900?1200 °C) from all CK chondrites; although, the isotopic compositions are somewhat variable. There is a fair correlation between the excess 15N values and the abundance of trapped 36Ar for the high-temperature component, suggesting presolar origin of these species. The light N (δ15N = ?106.8‰) observed in Karoonda is one of the lightest N components ever reported for bulk chondrites.  相似文献   

14.
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   

15.
We report the bulk C abundances, and C and O isotopic compositions of carbonates in 64 CM chondrites, 14 CR chondrites, 2 CI chondrites, LEW 85332 (C2), Kaba (CV3), and Semarkona (LL3.0). For the unheated CMs, the total ranges of carbonate isotopic compositions are δ13C ≈ 25–75‰ and δ18O ≈ 15–35‰, and bulk carbonate C contents range from 0.03 to 0.60 wt%. There is no simple correlation between carbonate abundance and isotopic composition, or between either of these parameters and the extent of alteration. Unless accretion was very heterogeneous, the uncorrelated variations in extent of alteration and carbonate abundance suggests that there was a period of open system behavior in the CM parent body, probably prior to or at the start of aqueous alteration. Most of the ranges in CM carbonate isotopic compositions can be explained by their formation at different temperatures (0–130 °C) from a single fluid in which the carbonate O isotopes were controlled by equilibrium with water (δ18O ≈ 5‰) and the C isotopes were controlled by equilibrium with CO and/or CH4 (δ13C ≈ ?33‰ or ?20‰ for CO‐ or CH4‐dominated systems, respectively). However, carbonate formation would have to have been inefficient, otherwise carbonate compositions would have resembled those of the starting fluid. A quite similar fluid composition (δ18O ≈ ?5.5‰, and δ13C ≈ ?31‰ or ?17‰ for CO‐ or CH4‐dominated systems, respectively) can explain the carbonate compositions of the CIs, although the formation temperatures would have been lower (~10–40 °C) and the relative abundances of calcite and dolomite may play a more important role in determining bulk carbonate compositions than in the CMs. The CR carbonates exhibit a similar range of O isotopes, but an almost bimodal distribution of C isotopes between more (δ13C ≈ 65–80‰) and less altered samples (δ13C ≈ 30–40‰). This bimodality can still be explained by precipitation from fluids with the same isotopic composition (δ18O ≈ ?9.25‰, and δ13C ≈ ?21‰ or ?8‰ for CO‐ or CH4‐dominated systems, respectively) if the less altered CRs had higher mole fractions of CO2 in their fluids. Semarkona and Kaba carbonates have some of the lightest C isotopic compositions of the meteorites studied here, probably because they formed at higher temperatures and/or from more CO2‐rich fluids. The fluids responsible for the alteration of chondrites and from which the carbonates formed were almost certainly accreted as ices. By analogy with cometary ices, CO2 and/or CO would have dominated the trapped volatile species in the ices. The chondrites studied are too oxidized for CO‐dominated fluids to have formed in their parent bodies. If CH4 was the dominant C species in the fluids during carbonate formation, it would have to have been generated in the parent bodies from CO and/or CO2 when oxidation of metal by water created high partial pressures of H2. The fact that the chondrite carbonate C/H2O mole ratios are of the order predicted for CO/CO2‐H2O ices that experienced temperatures of >50–100 K suggests that the chondrites formed at radial distances of <4–15 AU.  相似文献   

16.
Abstract— A glass separate from the LEW88516 shergottite was analyzed by step-wise combustion for N and noble gases to determine whether it contained trapped gas similar in composition to the martian atmosphere-like component previously observed in lithology C of EETA79001. Excesses of 40Ar and 129Xe were in fact observed in this glass, although the amounts of these excesses are ≤20% of those seen in the latter meteorite, and are comparable to the amounts seen in whole-rock analyses of LEW88516. The isotopic composition of N in LEW88516 does not show an enrichment in 15N commensurate with the amount of isotopically-heavy N expected from the noble gases excesses. One must posit some extreme assumptions about the nature of the N components present in LEW88516 in order to allow the presence of the trapped nitrogen component. Alternatively, the N has somehow been decoupled from the noble gases, and was either never present or has been lost.  相似文献   

17.
We have investigated the H and Cl systematics in apatite from four brecciated lunar meteorites. In Northwest Africa (NWA) 4472, most of the apatites contain ～2000–6000 ppm H2O with δD between ?200 and 0‰, except for one grain isolated in the matrix, which contains ～6000 ppm H2O with δD of ～500–900‰. This low‐δD apatite contains ～2500–7500 ppm Cl associated with δ37Cl of ～15–20‰, while the high‐δD grain contains ～2500 ppm Cl with δ37Cl of ～7–15‰. In NWA 773, apatites in a first group contain ～700–2500 ppm H2O with δD values averaging around ～0 ± 100‰, while apatites in a second group contain ～5500–16500 ppm H2O with δD ～250 ± 50‰. In Sayh al Uhaymir (SaU) 169 and Kalahari (Kal) 009, apatites are similar in terms of their H2O contents (～600–3000 ppm) and δD values (?100 to 200‰). In SaU 169, apatites contain ～6000–10,000 ppm Cl, characterized by δ37Cl of ～5–12‰. Overall, most of the analyzed apatite grains have δD within the range reported for carbonaceous chondrites, similar to apatite analyzed in ancient (>3.9 Ga) lunar magmatic. One grain in NWA 4472 has H and Cl isotope compositions similar to apatite from mare basalts. With an age of 4.35 Ga, this grain could be a representative of the oldest known lunar volcanic activity. Finally, since numerous evolved clasts in NWA 773 formed through silicate liquid immiscibility, the apatite grains with extremely high H2O contents, reaching pure hydroxylapatite composition, could provide insights into the effects of such process on the evolution of volatiles in lunar magmas.  相似文献   

18.
The nitrogen isotope ratio of middle atmosphere nitrogen oxide is predicted as a function of altitude. Nitrogen oxides originate photochemically either from stratospheric nitrous oxide reacting with O(1D) or in the mesosphere and thermosphere from direct dissociation of N2 and ionization-initiated reactions involving O2 and N2. During its formation process, N2O acquires a nitrogen isotopic composition of N isotopes different than N2. Photodissociation within the stratosphere also modifies the proportion of isotopes. Reaction of stratospheric NO with O3 produces NO2, which when photodissociated yields NO depleted in 15N relative to NO2 in laboratory air. The value of δ15NO in the stratosphere is −100‰. In the altitude region between 50 and 65 km, NO is transformed into NO2 and then returned to NO by reaction of NO2 with O and by NO2 photodissociation. These reactions determine the isotopic makeup of NO. Above 65 km, nitric oxide is produced by local ionization processes and gas phase photochemical reactions involving N2 and excited O2. These processes determine the isotopic composition of NO in the upper mesosphere and thermosphere. Here δ15NO is 0‰. Air transported into the mesosphere above 65 km will reflect the NO isotopic values of the region below, while mesospheric NO transported below 65 km will not be distinguishable from NO originating in the stratosphere.  相似文献   

19.
Abstract— We performed in situ morphological and isotopic studies of graphite in the primitive chondrites Khohar (L3), Mezö‐Madaras (L3), Inman (L3), Grady (H3), Acfer 182 (CH3), Acfer 207 (CH3), Acfer 214 (CH3), and St. Marks (EH5). Various graphite morphologies were identified, including book, veins, fibrous, fine‐grained, spherulitic, and granular graphite, and cliftonite. SIMS measurements of H, C, N, and O isotopic compositions of the graphites revealed large variations in the isotopic ratios of these four elements. The δ15N and δ13C values show significant variations among the different graphite types without displaying any strict correlation between the isotopic composition and morphology. In the Khohar vein graphites, large 15N excesses are found, with δ15Nmax ～+955‰, confirming previous results. Excesses in 15N are also detected in fine‐grained graphites in chondrites of the CH clan, Acfer 182, Acfer 207, and Acfer 214, with δ15N ranging up to +440‰. The 15N excesses are attributed to ion‐molecule reactions at low temperatures in the interstellar molecular cloud (IMC) from which the solar system formed, though the largest excesses seem to be incompatible with the results of some recent calculation. Significant variations in the carbon isotopic ratios are detected between graphite from different chondrite groups, with a tendency for a systematic increase in δ13C from ordinary to enstatite to carbonaceous chondrites. These variations are interpreted as being due to small‐ and large‐scale carbon isotopic variations in the solar nebula.  相似文献   

20.
Noble gases and nitrogen were measured in two adjacent samples each from the Raghunathpura (IIAB) and the Nyaung (IIIAB) iron meteorite falls. Light noble gases in both the meteorites were of pure cosmogenic origin. Using (3He/4He)c ratios and the production systematic of Ammon et al. ( 2009 ), we estimated the sample depth and meteoroid size for Nyaung (~8 cm depth in a ~15 cm radius object) and Raghunathpura (~12–14 cm depth in a ~25 cm object). We derived cosmic ray exposure ages of 1710 ± 256 Ma (for Nyaung, the highest reported so far for the IIIAB group) and 224 ± 34 Ma (for Raghunathpura). Variable amounts of trapped Kr and Xe were found in both meteorites. The phase Q‐like elemental ratio (84Kr/132Xe) suggests that the trapped component is of indigenous origin, and most likely hosted in the heterogeneously distributed micro‐inclusions of troilite/schreibersite. Trapped phase Q component is being reported for the first time, for a IIAB iron meteorite. Both meteorites showed light isotopic composition for nitrogen, and need at least two N components to explain the observed N isotopic systematic. Variable amounts of trapped noble gases and the presence of more than one N component suggest that the magmatic process that formed the parent body of these meteorites either could not completely homogenize or completely degas all the phases.  相似文献   

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