Atmospheric and juvenile noble gases in the Skaergaard layered igneous intrusion     

Stephen P Smith 《Geochimica et cosmochimica acta》1984,48(5):1033-1041

Gabbro and diorite from the Skaergaard layered igneous intrusion contain noble gases which are mixtures of atmospheric and juvenile components. Atmospheric noble gases predominate in samples that have undergone extensive oxygen isotope exchange with meteoric-hydrothermal water. The source of the atmospheric noble gas component is inferred to be the hydrothermal circulation system. A juvenile component with ${}^{40}\text{Ar}{}^{36}\text{Ar}\text{≥ 6100}$ and containing fission xenon is also present This component predominates in samples showing unaltered magmatic oxygen isotope compositions. Neon of atmospheric isotopic composition is associated with the juvenile radiogenic ⁴⁰Ar and fission xenon. The source of this second noble gas component may be either the crustal country rock or the upper mantle. If the neon is juvenile primordial neon from a mantle source region, terrestrial primordial ${}^{20}\text{Ne}{}^{22}\text{Ne}$ is the same as atmospheric to within 4%. However, subduction of atmospheric noble gases into the upper mantle may provide an alternate source of neon and other noble gases in the mantle.  相似文献   

Trapped solar wind noble gases and exposure age of Luna 16 lunar fines     

O Eugster  N Grögler  M.D Mendia  P Eberhardt  J Geiss 《Geochimica et cosmochimica acta》1973,37(9):1991-2003

He, Ne, Ar, Kr and Xe concentrations and isotopic abundances were measured in three bulk grain size fractions prepared from sample L-16-19, No. 120 (C level, 20–22 cm depth) returned by the Luna 16 mission. The expected anticorrelation between the concentrations of trapped solar wind noble gases and grain size is observed. Elemental abundances of solar wind trapped noble gases are similar to those previously found in corresponding grain size fractions of the Apollo 11 and 12 fines. The trapped ratio ${}^4\text{He}{}^{20}\text{Ne}$ varies in the soils from different lunar maria due to diffusion losses. A rough correlation of ${}^4\text{He}{}^{20}\text{Ne}$ with the proportion of ilmenite in these samples is apparent. The elemental and isotopic ratios of the surface correlated noble gases in Luna 16 resemble those previously found in Apollo fines. Based on ²¹Ne, ⁷⁸Kr and ¹²⁶Xe a cosmic ray exposure age of 360 my was determined. This age is similar to those obtained for the soils from other lunar maria.  相似文献   

Noble gases in E-chondrites     

Jane Crabb  Edward Anders 《Geochimica et cosmochimica acta》1981,45(12):2443-2464

Noble gas data are reported for 12 E-chondrites. Combined with literature data, they show that K-Ar ages are >4 Æ for 14 out of 18 meteorites, yet U, Th-He ages are often shorter, perhaps due to late, mild reheating. Cosmic-ray exposure ages differ systematically between types 4 and 6, with E4's mostly below 16 Myr and E6's above 30 Myr. This may mean that the E-chondrite parent body contains predominantly a single petrologic type on the (~ 1 km) scale of individual impacts, in contrast to the more thoroughly mixed parent bodies of the ordinary chondrites.The heavy noble gases consist of at least two primordial components: the usual planetary component (${}^{36}\text{Ar}{}^{132}\text{Xe}\text{~ 80}$) and a less fractionated, ‘subsolar’ component ($\text{2700 ≤}{}^{36}\text{Ar}{}^{132}\text{Xe}\text{≤ 3800}$). The latter is found in highest concentration in the E4 chondrite South Oman (³⁶Ar = 760 × 10^?8cc/g, ${}^{36}\text{Ar}{}^{132}\text{Xe}\text{= 2700}$). The isotopic compositions of both components are similar to typical planetary values, indicating that some factor other than mass controlled the noble gas elemental ratios. The heavy Xe isotopes occasionally show some of the lowest ${}^{134}\text{Xe}{}^{132}\text{Xe}$ and ${}^{136}\text{Xe}{}^{132}\text{Xe}$ ratios measured in bulk chondrites, suggestive of nearly fission-free Xe (e.g. ${}^{136}\text{Xe}{}^{132}\text{Xe}\text{= 0.3095 ± 0.0020}$). Amounts of planetary gas in E4 E6 chondrites fall in the range for ordinary chondrites of types 4–6, but, in contrast to the ordinary chondrites. fail to correlate with petrologic type or volatile trace element contents. Another unusual feature of E-chondrites is that primordial Ne is present even in most 4's and 5's (²⁰Ne_p ~ 1 to 7 × 10^?8cc/g). with an isotopic composition consistent with planetary Ne.Analyses of mineral separates show that the planetary gases are concentrated in an HF- and HCl-insoluble mineral similar to phase Q, the poorly characterized, HNO₃-soluble carrier of primordial gases in carbonaceous and ordinary chondrites. The subsolar gases, on the other hand, are located in an HCl- and HNO₃-resistant phase, possibly enstatite or a minor phase included in enstatite. Much of the ¹²⁹Xe_r (50% for E4's, > 70% for E6's) is in HCl-resistant but HF-soluble sites, suggestive of a silicate.A similar subsolar component may be responsible for the high ${}^{36}\text{Ar}{}^{132}\text{Xe}$ ratios of some C3's, unequilibrated ordinary chondrites, and the unique aubrite Shallowater. The planet Venus also has a high $\text{Ar}\text{Kr}$ ratio, well above the planetary range, and hence may have acquired its noble gases from an E-chondrite-like material, similar to South Oman.  相似文献   

On the siting of noble gases in E-chondrites     

Jane Crabb  Edward Anders 《Geochimica et cosmochimica acta》1982,46(11):2351-2361

We have investigated the siting of noble gases in 6 E-chondrites, by analyzing fractions separated by density, grain size, and chemical resistance from Qingzhen (E3), Indarch (E4), Abee and Saint Sauveur (E4-5) and Yilmia and North West Forrest (E6).The new “subsolar” (i.e. Ar-rich) component in E6's is concentrated in the main, ensatite-rich fraction of the meteorites, with density 3.06–3.3 g/cm³. It is unaffected by HCl and HNO₃ treatments of such fractions and remains in unchanged concentration when the samples are partially dissolved by HF. These properties suggest that the subsolar component is located in enstatite, or less likely, in a phase closely associated with it. E4-5's have at least half of their subsolar gases in HCl- and HNO₃-resistant sites (enstatite?), but fail to show the increasing gas concentration with decreasing grain size that is characteristic of most other primordial gas carriers. This may mean that the subsolar gases originally were in some other phase, but were then transferred to enstatite by metamorphism.Most of the ¹²⁹Xe_r of E6's is concentrated in the same fractions as the subsolar gases, again suggesting enstatite or an associated phase as the host. Only a few percent of the ¹²⁹Xe_r is contained in fractions enriched in other major and minor minerals. In E4's, on the other hand, ¹²⁹Xe_r is enhanced in finegrained, low density fractions and is also partly associated with chondrules. Perhaps ¹²⁹I was originally contained in fine-grained matrix, but was transferred to enstatite during metamorphism.A carbon-rich fraction of Indarch (E4) is enhanced in Ne-A, CCF-Xe, and L-Xe. Interestingly, both the isotopic composition of Xe and the Ne/CCF-Xe ratios resemble those of C-chondrites, yet these two meteorite classes probably formed rather far apart. Thus, if these components were mixed at a late stage, it must have been in fairly constant ratio over a large scale. Alternatively, they may have been mixed at an earlier stage, into a common carrier that was spread through a significant portion of the solar nebula.The primordial gases of Qingzhen (E3) resemble those of Indarch: they are present in moderate amounts (${}^{20}\text{Ne}{}_{\mathrm{p}}\text{= 1.2 × 10}{}^{\mathrm{?8}}\text{cc/g,}{}^{132}\text{Xe = 10 × 10}{}^{\mathrm{?10}}\text{cc/g)}$, with little or no contribution from the subsolar component. Thus Qingzhen reinforces our earlier finding that E-chondrites show no regular increase in noble gas content with decreasing petrologic type. One notable feature of Qingzhen is its very low ${}^3\text{He}{}^{21}\text{Ne}$ ratio of 1.07, which indicates that ³He has been lost by solar heating. Solar heating may also account for its low, discordant gas retention ages (U,Th-He age = 1.1 AE, KAr age = 3.2AE).  相似文献   

Isotopic anomalies of noble gases in meteorites and their origins—IV. C3 (Ornans) carbonaceous chondrites     

Leo Alaerts  Roy S Lewis  Edward Anders 《Geochimica et cosmochimica acta》1979,43(9):1421-1432

The C3O chondrites Kainsaz, Lancé and Ornans were studied by an acid dissolution technique, to characterize the noble-gas components in 3 mineral fractions: HF, HCl-solubles (99% of the meteorite), chromite and carbon (0.3–0.9%), and ‘phase Q’, a poorly characterized trace mineral (0.05–0.4%) containing most of the Ar, Kr, Xe. For all fractions, gas contents decline in the order Kainsaz > Lancé > Ornans; this trend parallels volatile contents but not heterogeneity of olivine composition or degree of metamorphism and seems to reflect progressively higher condensation temperatures from the solar nebula.Solubles contain nearly unfractionated Xe, and show ${}^{136}\text{Ar}{}^{132}\text{Xe}$ ratios up to 850. Hence the high $\text{Ar}\text{Xe}$ ratios (200–400) of bulk C3O chondrites must be due to an HF-soluble mineral (possibly magnetite). Phase Q contains ordinary planetary gases and a Ne component of ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{= 10.3 ± 0.4.}$Chromite and carbon contain Ne of ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{= 8.6 ± 0.1}$ and ‘CCF’ xenon (a peculiar component of possibly fissiogenic origin, enriched in the heavy isotopes but accompanied by a component enriched in the light isotopes).In all primitive chondrites, both the amount and the chemical separability of CCFXe parallel the abundance of promordial noble gases and other volatiles, such as C, N, Tl, Bi and In. The close correlation of CCFXe with various properties of undoubtedly local origin (volatile content, petrologic type, presence of ferrichromite and carbon, etc.) is more consistent with a local than with an extrasolar origin of this component. A volatile superheavy element seems to be the most plausible source, but the evidence is not conclusive.  相似文献   

Isotopic anomalies of noble gases in meteorites and their origins—VI. Presolar components in the Murchison C2 chondrite     

Leo Alaerts  Roy S. Lewis  Jun-ichi Matsuda  Edward Anders 《Geochimica et cosmochimica acta》1980,44(2):189-209

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Intensive sampling of noble gases in fluids at Yellowstone: I. Early overview of the data; regional patterns     

B.M. Kennedy  M.A. Lynch  J.H. Reynolds  S.P. Smith 《Geochimica et cosmochimica acta》1985,49(5):1251-1261

The Roving Automated Rare Gas Analysis (RARGA) lab of Berkeley's Physics Department was deployed in Yellowstone National Park for a 19 week period commencing in June, 1983. During this time 66 gas and water samples representing 19 different regions of hydrothermal activity within and around the Yellowstone caldera were analyzed on site. Routinely, the abundances of five stable noble gases and the isotopic compositions of He, Ne, and Ar were determined for each sample. In a few cases the isotopes of Kr and Xe were also determined and found to be of normal atmospheric constitution.Correlated variations in the isotopic compositions of He and Ar can be explained within the precision of the measurements by mixing of only three distinct components. The first component is of magmatic origin and is enriched in the primordial isotope ³He with ${}^3\text{He}{}^4\text{He}\text{≥ 16}$ times the air value. This component also contains radiogenic ⁴⁰Ar and possible ³⁶Ar with ${}^{40}\text{Ar}{}^{36}\text{Ar}\text{≥ 500}$, resulting in a ${}^3\text{He}{}^{36}\text{Ar}$ ratio ≥ 41,000 times the air value. The second component is assumed to be purely radiogenic ⁴He and ⁴⁰Ar (${}^{41}\text{He}{}^{401}\text{Ar}\text{= 4.08 ± .33}$). This component is the probable carrier of observed excesses of ²¹¹Ne, attributed to the α,n reaction on ¹⁸O. Its radiogenic character implies a crustal origin in U. Th, and Krich aquifer rocks. The third component, except for possible mass fractionation, is isotopically indistinguishable from the noble gases in the atmosphere. This component originates largely from infiltrating run-off water saturated with atmospheric gases.In addition to exhibiting nucleogenic ²¹¹Ne, Ne data show anomalies in the ratio ${}^{20}\text{Ne}{}^{20}\text{Ne}$, which correlate roughly with the ${}^{21}\text{Ne}{}^{22}\text{Ne}$ anomalies for the most part, but not as would occur from simple mass fractionation. Some exaggerated instances of the ${}^{20}\text{Ne}{}^{22}\text{Ne}$ anomaly occur which could be explained by combined mass fractionation of Ne and Ar isotopes to a severe degree coupled with remixing with normally isotopic gases. Otherwise exotic processes have to be invoked to explain the ²⁰Ne data.Relative abundances of the non-radiogenic and non-nucleogenic noble gases (²²Ne, ³⁶Ar, ⁸⁴Kr, and ¹³²Xe) are highly variable but strongly correlated. High Xe/Ar ratios are always accompanied by low Ne/ Ar ratios and vice versa. Except for water from the few cold (T < 20°C) springs analyzed, none of the samples have relative abundances consistent with air saturated water and the observed variations are not readily explained by the distillation of air saturated water.In characterizing each area of hydrothermal activity by the highest ${}^3\text{He}{}^4\text{He}$ ratio found for that area, we find that within the caldera this parameter is somewhat uniform at ~7 ± 1 times the air value. There are exceptions, most notably at Mud Volcano, an area located along a crest of recent and rapid uplift. Here the maximum ${}^3\text{He}{}^4\text{He}$ ratio is ~ 16 times the air value. Also noteworthy is Gibbon Basin which is in the vicinity of the most recent rhyolitic volcanism and exhibits a ${}^3\text{He}{}^4\text{He}$ ratio ~ 13 times the air value. Immediately outside the caldera the maximum $\text{sol}{}^3\text{He}{}^4\text{He}$ ratio decreases rapidly to values < ~3 times the air value.  相似文献   

Laboratory simulation of meteoritic noble gases. II. Sorption of xenon on carbon: Etching and heating experiments     

M.G. Zadnik  John F. Wacker  Roy S. Lewis 《Geochimica et cosmochimica acta》1985,49(4):1049-1059

Sixteen amorphous carbon (lampblack) samples that had been exposed to Xe¹²⁷ and pumped for >9 hrs to remove the most labile gas were examined by etching with HNO₃, for comparison with the release pattern of meteoritic xenon. Samples originally exposed at 100–200°C lost 90% of their Xe very readily, when the surface had been etched to a mean depth of only ~0.2 Å. This suggests that the Xe is adsorbed mainly at rare sites that are unusually reactive to HNO₃. The adsorbed Xe survived several months' storage in vacuum, but on exposure to air, part of it was lost within a few hours, while the remainder persisted without measurable exchange. Samples exposed at 800–1000°C had a similar adsorbed component, as well as a second, tightly bound component extending to a mean depth of up to 30 Å; this component had apparently diffused into the carbon during exposure. The (microscopic) diffusion coefficient for graphitic crystallites is 5 × 10^?20 cm²/sec at 1000°C.PVDC carbon lost its adsorbed Xe at about the same rate as lampblack on exposure to air or HNO₃, though it differs from lampblack in being non-graphitizable and more porous. It had only a small diffused component, however.The most tightly bound part of the Xe adsorbed on lampblack resembles planetary Xe in most characteristics: surface siting, etchability, persistence in vacuum, and lack of exchange with atmospheric Xe. The Xe concentrations—if interpreted as equilibrium distribution coefficients—are some 10⁶× too small to account for meteoritic Xe, but it appears that equilibrium had not been reached by any of the samples, even after 1 day's exposure to Xe. If the uptake of Xe is controlled by rate rather than equilibrium, then the high noble gas concentrations in meteorites may simply reflect the much longer uptake times in the solar nebula. It seems likely that the trapping mechanisms discussed here can also explain two other features: elemental fractionations of noble gases, and the close correlation between planetary Xe and CCFXe.  相似文献   

The solubility of noble gases in water and in NaCl brine     

S.P. Smith  B.M. Kennedy 《Geochimica et cosmochimica acta》1983,47(3):503-515

A direct-sampling, mass-spectrometric technique has been used to measure simultaneously the solubilities of He, Ne, Ar, Kr, and Xe in fresh water and NaCl brine (0 to 5.2 molar) from 0° to 65 °C, and at 1 atm total pressure of moist air. The argon solubility in the most concentrated brines is 4 to 7 times less than in fresh water at 65 °C and 0°C, respectively. The salt effect is parameterized using the Setschenow equation. where M is NaCl moiarity, βⁱ_o(T) and βⁱ(T) the Bunsen solubility coefficients for gas i in fresh water and brine, and Kⁱ_M(T) the empirical salting coefficient. Values of Kⁱ_M(T) are calculated using volumetric concentration units for noble gas and NaCl content and are independent of NaCl molarity. Below about 40°C, temperature coefficients of all Kⁱ_M are negative. The value of K^He_M is a minimum at 40°C. K^Ar_M decreases from about 0.40 at 0°C to 0.28 at 65 °C. The absolute magnitudes of the differences in salting coefficients (relative to K^Ar_M) decrease from 0° to 65°C. Over the range of conditions studied, all noble gases are salted out, and K^He_M ? K^Ne_M < K^Ar_M < K^Kr_M < K^Xe_M.From the solubility data, we calculated $\text{Δ}\text{G}{}^0{}_{\mathrm{tr}}$, $\text{Δ}\text{S}{}^0{}_{\mathrm{tr}}$, $\text{Δ}\text{H}{}^0{}_{\mathrm{tr}}$ and $\text{Δ}\text{C}{}^{\mathrm{O}}{}_{\mathrm{p,tr}}$ for the transfer of noble gases from fresh water to 1 molar NaCl solutions. At low temperatures $\text{Δ}\text{S}{}^0{}_{\mathrm{tr}}$, is positive, but decreases and becomes negative at temperatures ranging from about 25°C for He to 45°C for Xe. At low temperatures, the dissolved electrolyte apparently interferes with the formation of a cage of solvent molecules about the noble gas atom. At higher temperatures, the local environment of the gas atom in the brine appears to be slightly more ordered than in pure water, possibly reflecting the longer effective range of the ionic fields at higher temperature.The measured solubilities can be used to model noble gas partitioning in two-phase geothermal systems at low temperatures. The data can also be used to estimate the temperature and concentration dependence of the salt effect for other alkali halides. Extrapolation of the measured data is not possible due to the incompletely-characterized minima in the temperature dependence of the salting coefficients. The regularities in the data observed at low temperatures suggest relatively few high-temperature data will be required to model the behavior of noble gases in high-temperature geothermal brines.  相似文献   

Colloidally separated samples from Allende residues: Noble gases,carbon and an ESCA-study     

Ulrich Ott  Johann Kronenbitter  Jose Flores  Sherwood Chang 《Geochimica et cosmochimica acta》1984,48(2):267-280

A non-colloidal fraction separated by physical means from an $\text{HF}\text{HCl}$-resistant residue of the Allende carbonaceous meteorite exhibits a ratio of isotopically “normal” (Q-type) xenon to “anomalous” xenon (X-type) that is ~4 times larger than usually observed. Coincidentally this fraction contains carbon that is isotopically heavier by ~10%. than bulk Allende residue samples. ESCA analyses of companion colloidal separates show that the major portion of the S contained in our $\text{HF}\text{HCl}$-residues is elemental rather than a sulfide. They also confirm earlier observations that no elementally distinct surface coating is present, in accord with the absence of a surface-sited sulfur-bearing gas carrier, and that the oxygen content is increased after etching with nitric acid. For these separates noble gas data coupled with the ESCA data for nitrogen and the isotopic data for carbon point to the existence of heterogeneities among the noble gas-, carbon- and nitrogen-bearing phases and, thus, preservation of discrete components from the variety of source regions (or production mechanisms, or both) sampled by the Allende parent body. In sharp contrast to the success of physical and chemical methods in yielding samples in which one of the major noble gas components predominates to an extraordinary degree over the other, carbon isotopic compositions that have been inferred for the respective carrier phases in these same samples are strongly contradictory. Mass and isotope balance considerations lead us to conclude that a major fraction of the carbonaceous matter in Allende is noble-gas-poor, a result that could be confirmed by direct isolation of a sample, the carbon in which is dominated by this variety; and for that reason no simple relationship is discernable yet between observed isotopic compositions and either major noble gas component. Similar ambiguities may exist for nitrogen. The possible relationship between carbon-rich phases in ureilites and carbonaceous chondrites is considered.  相似文献   

Variability of the He³ and Ne²¹ production rates in ordinary chondrites     

G.F Herzog 《Geochimica et cosmochimica acta》1973,37(9):2125-2133

Al²⁶ and noble gas contents of 6 ordinary chondrites with $\text{He}{}^3\text{Ne}{}^{21}$ ratios above 6.0 or below 4.0 are used to infer the variability of the production rates of He³ and Ne²¹ (P_He³ and P_Ne²¹). The ratio of the observed Al²⁶ content to a calculated, normal value is taken as a measure of the change of P_Ne²¹ from its normal value. The corresponding change in P_He³ is then computed from the observed $\text{He}{}^3\text{Ne}{}^{21}$ ratio and an average value of P_He³.According to these calculations which exclude orbital effects, P_He³ will be near the average value in meteorites with high $\text{He}{}^3\text{Ne}{}^{21}$ ratios, while P_Ne²¹ will be about 30 per cent below normal. In meteorites with low $\text{He}{}^3\text{Ne}{}^{21}$ ratios, P_He³ may be depressed by as much as 25 per cent from normal while P_Ne²¹ may be 15–20 per cent above the average.  相似文献   

Inert gases in a terra sample: measurements in six grain-size fractions and two single particles from Luna 20     

D Heymann  S Lakatos  J.R Walton 《Geochimica et cosmochimica acta》1973,37(4):875-885

The inert gases have been measured in six size fractions covering the range below 500 μm, in a single feldspathic fragment weighing 523 μg, and in an agglutinate particle weighing 465 μg. The two size fractions between 125 and 250 μm as well as 250 and 500 μm were separated into magnetic and non-magnetic portions, which were measured separately. Like the Apollo and Luna 16 fines, the terra fines represented by Luna 20 are very rich in trapped solar-wind gases, but they contain relatively less He⁴ and Ne²⁰, which is revealed by their average $\text{He}{}^4\text{Ne}{}^{20}$ ratio of 35 and $\text{Ne}{}^{20}\text{Ar}{}^{36}$ ratio of 2.9. Obviously the terra materials are less retentive for solar-wind He and Ne than typical mare fines such as 10084. Whether this is due to the relatively small TiO₂ or the relatively large plagioclase content of the former is not resolved. ($\text{Ar}{}^{36}\text{Kr}{}^{84}\text{)}{}_{\mathrm{trapped}}$ and ($\text{Ar}{}^{36}\text{Xe}{}^{132}\text{)}{}_{\mathrm{trapped}}$ ratios are relatively large; the average values are 2800 and 14400, respectively. The apparent Ne²¹ radiation ages of all the size fractions are in the range 209–286 × 10⁶ yr; the average is 260 × 10⁶ yr. This is in the range of values known for the Apollo and Luna 16 fines. The feldspathic fragment has a much greater apparent Ne_c²¹ age of 780 × 10⁶ yr. The Ar⁴⁰-Ar³⁶ systematic reveals the presence of two Ar⁴⁰ components, because Ar⁴⁰ = (1.41 ± 0.076)Ar³⁶ + (0.490 ± 0.130) × 10^?4 (cm³ STP/g). The $\text{Ar}{}^{40}\text{Ar}{}^{36}$ slope of 1.41 is not inconsistent with an origin of the sample from a relatively old terra region.  相似文献   

Isotopic anomalies of noble gases in meteorites and their origins—III. LL-chondrites     

Leo Alaerts  Roy S Lewis  Edward Anders 《Geochimica et cosmochimica acta》1979,43(9):1399-1415

Nine LL-chondrites were studied by a selective etching technique, to characterize the noblegas components in three mineral fractions: HF-HCl-solubles (silicates, metal, troilite, etc.; comprising ～ 99% of the meteorite), chromite and carbon (～ 0.3–0.7%) and Q (a poorly characterized mineral defined by its solubility in HNO₃, comprising ～ 0.05% of the meteorite but containing most of the Ar, Kr, Xe and a neon component of ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{= 10.9 ± 0.8}$). The ${}^{20}\text{Ne}{}^{36}\text{Ar}$ ratio in Q falls wi petrologic type and rising ³⁶Ar content, as expected for condensation from a cooling solar nebula, but contrary to the trend expected for metamorphic losses. Chondrites of different petrologic types therefore cannot all be derived from the same volatile-rich ancestor, but must have formed over a range of temperatures, with correspondingly different intrinsic volatile contents.The CCFXe (carbonaceous chondrite fission) component varies systematically with petrologic type. The most primitive LL3s (Krymka, Bishunpur, Chainpur) contain substantial amounts of CCFXe in chromite-carbon, enriched relative to primordial Xe as shown by high ${}^{136}\text{Xe}{}^{132}\text{Xe}$ (0.359–0.459, vs 0.310 for primordial Xe). These are accompanied by He and by Ne with ${}^{20}\text{Ne}{}^{22}\text{Ne}\text{≈ 8.0}$ and by variable amounts of a xenon component enriched in the light isotopes. The chromite in these meteorites is compositionally peculiar, containing substantial amounts of Fe(III). These meteorites, as well as Parnallee (LL3) and Hamlet (LL4) also contain CCFXe in phase Q, heavily diluted by primordial $\text{Xe}\text{(}{}^{136}\text{Xe}{}^{132}\text{Xe}\text{= 0.317–0.329)}$. On the other hand, LL5s and 6s (Olivenza, St. Séverin, Manbhoom and Dhurmsala) contain no CCFXe in either mineral. This deficiency must be intrinsic rather than caused by metamorphic loss, because Q in these meteorites still contains substantial amounts of primordial Ne.If CCFXe comes from a supernova, then its distribution in LL-chondrites requires three presolar carrier minerals of the right solubility properties, containing three different xenon components in certain combinations. These minerals must be appropriately distributed over the petrologic types, together with locally produced Q containing primordial gases, and they must be isotopically normal, in contrast to the gases they contain. On the other hand, if CCFXe comes from fission of a volatile superheavy element, then its decrease from LL3 to LL6 can be attributed to progressively less complete condensation from the solar nebula. Ad hoc assumptions must of the host phase Q, its association with ferrichromite and the origin of the associated xenon component enriched in the light isotopes.Soluble minerals in LL3s and LL4s contain a previously unobserved, solar xenon component, which, however, is not derived from the solar wind. Three types of ‘primordial’ xenon thus occur side-by-side in different minerals of the same meteorite: strongly fractionated Xe in ferrichromite and carbon, lightly fractionated Xe in phase Q, and ‘solar’ Xe in solubles. Because the first two can apparently be derived from the third by mass fractionation, it seems likely that all were trapped from the same solar nebula reservoir, but with different degrees of mass fractionation.  相似文献   

Noble gas evidence for two fluids in the Baca (Valles Caldera) geothermal reservoir     

S.P. Smith  B.M. Kennedy 《Geochimica et cosmochimica acta》1985,49(4):893-902

Noble gas elemental and isotopic abundances were measured in steam from four wells in the Baca geothermal reservoir located in the Valles Caldera, New Mexico. The ${}^{40}\text{Ar}{}^{36}\text{Ar}$ ratio and noble gas elemental abundances relative to ³⁶Ar are all strongly correlated with 1/³⁶Ar, the inverse of the argon content. Ratios of (α,n)-produced ²¹Ne1 and radiogenic ⁴⁰Ar1 to total ⁴He (dominantly radiogenic) are nearly constant at 2.1 × 10?8 and 0.20, respectively. The ${}^3\text{He}{}^4\text{He}$ ratio covers a restricted range of 3.9 to 4.8 times atmospheric. The high ³He content of the gas indicates the presence of a helium component ultimately derived from the mantle. Kr and Xe isotopic compositions are close to atmospheric; excess ¹²⁹Xe1 is <0.25% of the total ¹²⁹Xe.The high degree of linear correlation among the various noble gas results strongly suggests that the Baca reservoir contains two distinct fluids that are produced in varying proportions from individual wells. The noble gases in fluid A (~2900 mg/1 C1) are air-like, but with lighter gases and isotopes preferentially enriched. The fluid A ³⁶Ar content is low, only 13% that of 10°C air-saturated water (ASW). The second fluid, B (~ 1700 mg/1 C1), is the dominant carrier of the radiogenic and mantle-derived gases. The heavier non-radiogenic gases are preferentially enriched in fluid B, and its ³⁶Ar content is very low, only 5–7% ASW. The source of the noble gases in fluid A is tentatively ascribed to leaching of the relatively young (<1.4 m.y.) volcanic Bandelier Tuff. The radiogenic gases and mantle-derived helium in fluid B suggest a deeper source, possibly including gases escaping from a magma.  相似文献   

Trapping of xenon in ice: implications for the origin of the Earth's noble gases     

John F Wacker  Edward Anders 《Geochimica et cosmochimica acta》1984,48(11):2373-2380

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Noble-gas-rich separates from ordinary chondrites     

Robert Keith Moniot 《Geochimica et cosmochimica acta》1980,44(2):253-271

Acid-resistant residues were prepared by HCl-HF demineralization of three H-type ordinary chondrites: Brownfield 1937 (H3), Dimmitt (H3,4), and Estacado (H6). These residues were found to contain a large proportion of the planetary-type trapped Ar, Kr, and Xe in the meteorites. The similarity of these acid residues to those from carbonaceous chondrites and LL-type ordinary chondrites suggests that the same phase carries the trapped noble gases in all these diverse meteorite types. Because the H group represents a large fraction of all meteorites, this result indicates that the gas-rich carrier phase is as universal as the trapped noble-gas component itself. When treated with an oxidizing etchant, the acid residues lost almost all their complement of noble gases. In addition, the Xe in at least one oxidized residue, from Dimmitt, displayed isotopic anomalies of the type known as CCFX or DME-Xe, which is characterized by simultaneous excesses of both the lightest and heaviest isotopes. The anomaly in the Dimmitt sample differs from that observed in carbonaceous-chondrite samples, however, in the relative proportions of the light- and heavy-isotope excesses.The results of this study do not show an inverse correlation between trapped ${}^{20}\text{Ne}{}^{36}\text{Ar}$ and trapped ³⁶Ar abundance, as has been reported for acid-resistant residues from LL-chondrites. The results of this work therefore fail to support the hypothesis that meteoritic trapped noble gas abundances were established at the time of condensation.  相似文献   

On the calculation of cosmic-ray exposure ages of stone meteorites     

Philip J. Cressy  Donald D. Bogard 《Geochimica et cosmochimica acta》1976,40(7):749-762

Abundances of cosmic ray-produced noble gases and ²⁶Al, including some new measurements, have been compiled for some 23 stone meteorites with exposure ages of < 3 × 10⁶ yr. Concentrations of cosmogenic He, Ne, and Ar in these meteorites have been corrected for differences in target element abundances by normalization to L-chondrite chemistry. Combined noble gas measurements in depth samples of the Keyes and St. Séverin chondrites are utilized to derive equations for normalizing the production rates of cosmogenic ³He, ²¹Ne, and ³⁸Ar in chondrites to an adopted ‘average’ shielding: ${}^{22}\text{Ne}{}^{21}\text{Ne}\text{= 1.114.}$ The measured unsaturated ²⁶Al concentrations and the calculated equilibrium ²⁶Al for these meteorites are combined to estimate exposure ages. These exposure ages are statistically compared with chemistry- and shielding-corrected concentrations of cosmogenic He, Ne, and Ar to derive absolute production rates for these nuclides. For L-chondrites, at ‘average’ shielding, these production rates (in 10^?8 cm³/g 10⁶ yr) are: ³He = 2.45,²¹Ne = 0.47, and ³⁸Ar = 0.069, which are ~ 25% higher than production rates used in the past. From these production rates and relative chemical correction factors, production rates for other classes of stone meteorites are derived.  相似文献   

Laboratory simulation of meteoritic noble gases. I. Sorption of xenon on carbon: Trapping experiments     

John F. Wacker  M.G. Zadnik  Edward Anders 《Geochimica et cosmochimica acta》1985,49(4):1035-1048

We have studied trapping of radioactive ¹²⁷Xe in three types of carbon: carbon black (lamp black  LB), pyrolyzed polyvinylidene chloride (PVDC), and pyrolyzed acridine (C₁₃H₉N). A total of 86 samples were exposed to Xe at T between 100 and 1000°C, for times between 5 min and 240 hours, at p_xe ~ 5 × 10^?7 atm. Excess gas phase and loosely sorbed Xe were pumped away and the remaining, tightly bound Xe was measured by γ-spectrometry.At 100°C,× >90% of the Xe desorbs within a few minutes' pumping but a small amount remains even after 4000 min. Distribution coefficients for this tightly bound Xe are ~1 × 10^?2, 1 and 10 ccSTP/g atm for LB, acridine and PVDC carbons. The tightly bound Xe consists of two components. One occurs over the entire range 100–1000°C, becoming less abundant at high T; it appears to be physisorbed. The other occurs only at T > 500°C and is probably due to volume diffusion. The adsorbed component in LB has an apparent ΔH between ?2.3 and ?5.7 kcal/mole. The diffused component, which occurs in LB and possibly in acridine carbon, has an activation energy Q = 27 ± 8 kcal/mole and a diffusion coefficient D = 1.3 × 10^?17 cm²/sec at 1000°C. These values are comparable to those found for other types of amorphous carbon (Morrisonet al., 1963; Nakai et al., 1960).The low-T component displays two paradoxical features: low ΔH_ads, in the range for Xe physisorbed on carbon, but exceedingly long adsorption or desorption times (~10³ min at 100–400 or 1000°C). Although these long times seem to suggest a high energy process such as chemisorption, our results are best explained by a model that invokes physisorption within a labyrinth of micropores—of atomic dimensions—known to exist in amorphous carbons. The long adsorption/desorption times reflect either the long distances (~5 cm) Xe atoms must migrate by random walk to enter or leave the labyrinth, or the long times needed for Xe atoms to traverse tight spots or constricted pores that connect interior and exterior surfaces of the carbon (activated entry). Both variants of this model predict long equilibration times for the observed ΔH_ads of ?2 to ?6 kcal/mole. Apparently, xenon can be tightly trapped in carbon without resorting to high-energy bonding or to exotic mechanisms.These results suggest that “planetary” type noble gases in meteorites, located at or near grain surfaces of amorphous carbon, may be trapped by adsorption in micropores, whereas components such as CCFXe, which are uniformly distributed in their carrier phases, may be trapped by mechanisms such as volume diffusion or ion implantation.  相似文献