Chemical fractionations in meteorites—VI. Accretion temperatures of H-, LL- and E-chondrites,from abundance of volatile trace elements     

J.C. Laul  R. Ganapathy  Edward Anders  John W. Morgan 《Geochimica et cosmochimica acta》1973,37(2):329-357

Extending our earlier work on 11 L-chondrites, we have measured 9 volatile elements (Ag, Bi, Cs, In, Rb, Tl, Se, Cd, Zn) by neutron activation analysis in 11 LL- and 10 E-chondrites; the first 6 elements also in 22 H-chondrites. The observed fractionation patterns are consistent with theoretical condensation curves and hence were apparently established during condensation from the solar nebula. Ordinary chondrites seem to have accreted between 420 and 500°K at $\text{P ≈ 10}{}^{\mathrm{?5}}$ atm; enstatite chondrites, at 460 to 520°K and P ≈ 5 x? 10^?4 atm. The values for ordinary chondrites agree with O¹⁸-based temperatures by Onuma. et al. (1972) and with other characteristics such as Fe²⁺ content, presence of FeS and absence of Fe₃O₄.A few detailed trends were noted. Seven of the 54 meteorites seem to contain small amounts of a material enriched in Ag, Bi and especially T1; possibly a late condensate from a region depleted in metal. Silver shows considerable scatter, which suggests inhomogeneous distribution in the meteorites. Xenon correlates with In approximately as expected for equilibrium solubility, with some differences (petrologic type 3; E-chondrites) attributable to mineralogical factors. Meteorites of higher petrologic types are slightly deficient in Xe, probably due to gas losses during metamorphism. Cesium also appears to have been redistributed during metamorphism.Various features of the two-component model are critically examined in the light of the latest evidence. Apparently this model still is an adequate approximation of reality.  相似文献   

Isotopic anomalies of noble gases in meteorites and their origins—VII. C3V carbonaceous chondrites     

Jun-Ichi Matsuda  Roy S. Lewis  Hiroshi Takahashi  Edward Anders 《Geochimica et cosmochimica acta》1980,44(11):1861-1874

Noble gases were measured in bulk samples of the C3V chondrites Grosnaja, Vigarano, and Leoville, and in HF,HCl-insoluble residues before and after etching with HNO₃. The residues were characterized by INAA and SEM. Gas components were determined, directly or by subtraction, for the following fractions: HF,HCl-solubles (?98% of the meteorite), ‘sphase Q’, a poorly characterized trace mineral that is insoluble in HCl-HF but soluble in HNO₃, and an insoluble residue, consisting of ferrichromite, carbonaceous matter, and spinel.Bulk meteorites show some correlation of the noble-gas pattern with McSween's subclasses: two ‘oxidized’ C3V's—Allende (LEWIS et al, 1975) and Grosnaja— have lower Ar/Xe but higher Ne/Xe ratios than the ‘reduced’ C3V's—Vigarano and Leoville—which are transitional to LL3's and C3O chondrites in both respects. An HCl-soluble mineral of high Ar/Xr ratio seems to be responsible. In other respects, the 3 C3V's of this study resemble Allende, with only moderate differences. Phase Q contains most of the Ar, Kr, Xe, but only small amounts of Ne; the etched residues contain planetary Ne ($\text{Ne}{}^{20}\text{Ne}{}^{22}\text{? 8.5}$) and the controversial CCFXe component, enriched in the heavy Xe isotopes ($\text{Xe136}\text{Xe132 ? 0.4–0.5}$). The CCFXe is accompanied by an ‘L-Xe’ component that is enriched in the light Xe isotopes. The proportion of the two is virtually constant in C3V's. as in all other C-chondrites. in contrast to the ~ 2-fold variation in ordinary chondrites.C3V's have systematically higher $\text{Xe}{}^{136}\text{Xe}{}^{132}$ ratios, and hence higher ratios of CCFXe to planetary Xe, than do other chondrite classes. This may reflect some peculiarity in their formation conditions, favoring uptake of CCFXe.  相似文献   

Extinct I129 in C3 chondrites     

Jane Crabb  Roy S. Lewis  Edward Anders 《Geochimica et cosmochimica acta》1982,46(12):2511-2525

Eight C3 chondrites were examined by the I¹²⁹Xe¹²⁹ dating method, to see whether their IXe “ages” (better, initial $\text{I}{}^{129}\text{I}{}^{127}$ratios ≡ R₀) correlate with any other properties. The R₀'s range from 1.60 × 10^?4 to 1.09 × 10^?4, corresponding to IXe ages from 2.0 Myr before to 6.7 Myr after Murchison magnetite. Three C3O's (Lancé, Felix, Ornans) have essentially indistinguishable R₀'s of (1.41 ± 0.13) to (1.17 ± 0.10) × 10^?4; the fourth C3O, Warrenton, is undatable owing to homogenization of radiogenic and trapped Xe.Four C3V's show a distinct spread: Vigarano and Grosnaja are highest [R₀ = (1.60 ± 0.07) and (1.57 ± 0.14) × 10^?4], Mokoia is intermediate, and Kaba is lowest [R₀ = (1.38 ± 0.06) and (1.09 ± 0.10) × 10^?4]. Literature values for Allende place it near Kaba. These R₀'s correlate inversely with 4 other properties: I-, Br-, and Cd-content, and olivine composition, both percent mean deviation (PMD) and proportion of iron-poor olivine grains (≤2% fayalite).It is difficult to accept the ～9 Myr spread in R₀ as a true age, reflecting either nebular or parent-body processes. This time span is more than an order of magnitude longer than the lifetime of the solar nebula inferred from astronomical evidence. Nor does the degree of thermal metamorphism, which is slight for C3's anyway, correlate with R₀. A more plausible interpretation is that the variations in R₀ reflect mainly isotopic heterogeneity of iodine. The simplest model that accounts for the correlations with R₀ involves mixing of two iodine components in the solar nebula, associated with gas and grains, respectively. The second, of lower $\text{I}{}^{129}\text{I}{}^{127}$ ratio, predominated at later times and thus became enriched in late-formed meteorites, along with other volatiles such as Cd and Br. The low Fe content and large PMD of olivine may reflect either less metamorphism owing to shallow location in the parent body, or greater reduction of Fe²⁺ during chondrule formation.  相似文献   

Chronology and petrogenesis of young achondrites,Shergotty, Zagami,and ALHA77005: late magmatism on a geologically active planet     

C.-Y. Shih  L.E. Nyquist  D.D. Bogard  G.A. McKay  J.L. Wooden  B.M. Bansal  H. Wiesmann 《Geochimica et cosmochimica acta》1982,46(11):2323-2344

A study was undertaken to determine the chronology, petrogenesis and relationships among the shergottites, Shergotty and Zagami and the unique achondrite ALHA77005. These meteorites are the product of a variety of complex processes.Petrogenesis: Chondrite-normalized abundance patterns of Shergotty and Zagami are very similar and show pronounced depletions of both the light REE (La-Nd) and heavy REE (Dy-Lu) relative to Sm-Gd. These characteristic depletions are even more pronounced for ALHA77005. The light REE depletion is qualitatively consistent with the presence of cumulus pyroxene and/or olivine in these meteorites, but trace element models show that the parental magmas of all three meteorites were probably also light REE depleted. Both trace element model calculations and combined Rb-Sr and Sm-Nd isotopic systematics show that the meteorites could not have been co-magmatic nor can ALHA77005 be representative of the source material of the shergottites. Light REE depletion of the parental magmas also implies light REE depletion of the source material. The Sm-Nd systematics of the shergottites require a time-averaged sub-chondritic (light REE enriched) Sm-Nd ratio since 4.6 AE ago. The Sm-Nd systematics of ALHA77005 permit a time-averaged super-chondritic (light REE depleted) Sm/Nd ratio if its crystallization age is less than T_ICE = 0.72 AE.Chronology. Rb-Sr internal isochrons for all three meteorites and a Sm-Nd internal isochron for Zagami are concordant at ~ 180 Myr. ³⁹Ar-⁴⁰Ar plateau ages of Shergotty and Zagami maskelynite are ~250–260 Myr. These ages apparently reflect resetting of these isotopic systems by shock metamorphism which converted the feldspar to maskelynite. The concordance of these ages suggests a single shock event during which the meteorites were in close physical proximity. The time of this event is most precisely given by the Rb-Sr age of 180 ± 4 Myr for Zagami.The crystallization ages of the meteorites were not precisely determined. Extreme upper limits are determined by Sm-Nd model ages relative to an eucrite initial ${}^{143}\text{Nd}{}^{144}\text{Nd = 0.505835}$ at 4.6 AE ago. These model ages for Shergotty, Zagami and ALHA77005 are 3600, 3500 and 2850 Myr, respectively. The Sm-Nd whole rock age of 1340 ± 60 Myr for the three meteorites gives the crystallization age if the Sm/Nd ratios of the precursor materials were always the same. We consider this 1340 Myr age as a “best estimate” upper limit. “Best estimate” lower limits for Shergotty and Zagami are taken from the average ³⁹Ar-⁴⁰Ar ages of 1200 and 900 Myr of pyroxene separates. The average ³⁹Ar-⁴⁰Ar age of a whole rock sample of ALHA77005 was 1600 Myr and can be partitioned between a low temperature (feldspar) phase and a high temperature (olivine + pyroxene + inclusions) “phase”. The average apparent ³⁹Ar-⁴⁰Ar age of the low temperature phase is ~1050 Myr, which is chosen as the “best estimate” lower limit to the age. The crystallization ages of Shergotty, Zagami and ALHA77005 probably lie within the ranges of 1200–1300, 900–1300 and 1000–1300 Myr, respectively. The Rb-Sr whole rock age of 4400 ± 400 Myr and single-stage BABI model ages of ~4800–5100 Myr are interpreted as reflecting differentiation of the parent body at ~4600 Myr ago.The complex geochemical and isotopic evolution recorded by these meteorites suggests a geologically active parent body capable of sustaining melting at two or more epochs in its history.  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   

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   

The behavior of actinides,phosphorus, and rare earth elements during chondrite metamorphism     

M.T Murrell  D.S Burnett 《Geochimica et cosmochimica acta》1983,47(11):1999-2014

New data on the U, Pu, and P distributions in less metamorphosed H-chondrites (type 3–5), coupled with literature results, permit a provisional picture to be assembled of the chemistry of these elements and for the rare earth elements in ordinary chondrites and the changes brought about by chondritic metamorphism. Preferential associations of phosphates with metals and/or sulndes in all chondrites strongly indicate an “initially” siderophile or conceivably chalcophile character for P in ordinary chondrite precursor materials with phosphate subsequently formed by oxidation. This oxidation occurred prior to or during chondritic metal-silicate fractionation. Uranium is initially concentrated in chondrule glass at ~ 100 ppb levels with phosphates (primarily merrillite) in H-3 chondrites being essentially U-free (<20 ppb). As chondrule glass devitrified during metamorphism, U migrated into phosphates reaching ~ 50 ppb in Nadiabondi (H-5) merrillite and 200–300 ppb in merrillite from equilibrated chondrites but “froze out” before total concentration in phosphates occurred. Relative ²⁴⁴Pu fission track densities in the outer 5 μm of olivine and pyroxene grains in contact with merrillite and with chondrule mesostasis in Bremervörde (H-3) give Pu(mesostasis)/Pu(merrillite) <0.01, implying total concentration of Pu in phosphates. Similarly, no detectable Pu (<0.1 ppb) was found in chondrule mesostasis in Tieschitz and Sharps; whereas, direct measurements of tracks in phosphates in H-3 chondrites are consistent with high (?10 ppb) Pu concentrations. Thus, a strong Pu-P correlation is indicated for ordinary chondrites. There is variable Pu/U fractionation in all chondritic phosphates reaching an extreme degree in the unequilibrated chondrites; therefore, the Pu/U ratio in phosphates appears relatively useless for relative meteorite chronology. Literature data indicate that the REE are located in chondrules in unequilibrated chondrites, most likely in glass; thus there may also be strong Pu/Nd fractionation within these meteorites. Like U, the REE migrate into phosphates during metamorphism but, unlike U, appear to be quantitatively concentrated in phosphates in equilibrated chondrites. Thus relative ages, based on Pu/Nd, may be possible for equilibrated chondrites, but the same chronological conclusions are probably obtainable from Pu concentrations in phosphates, i.e., on the Pu/P ratio. However, Pu/P chronology is possible only for ordinary chondrites; so there appears to be no universal reference element to cancel the effects of Pu chemical fractionation in all meteorites. Available data are consistent with — but certainly do not prove-that variations in Pu/P represent age differences, but if these age differences do not exist, then it is conceivable that the solar system ${}^{244}\text{Pu}{}^{238}\text{U}$ ratio, important for cosmochronology, is still lower than the presently accepted value of 0.007.  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   

${}^{40}\text{Ar}{}^{39}\text{Ar}$ dating,Ar diffusion properties,and cooling rate determinations of severely shocked chondrites     

D.D. Bogard  W.C. Hirsch 《Geochimica et cosmochimica acta》1980,44(11):1667-1682

Determinations of ${}^{40}\text{Ar}{}^{39}\text{Ar}$ ages are reported for seven severely shock-heated chondrites. Shaw gives a plateau age of 4.29 Gyr. Louisville, Farmington, and Wickenburg give well-defined intercept ages of 0.5–0.6 Gyr. Orvinio, Arapahoe, and Lubbock show complex ${}^{40}\text{Ar}{}^{39}\text{Ar}$ release curves, with age minima of 0.7–1.0 Gyr. Degassing times of 0.5–1.0 Gyr are suggested for these meteorites. Most severely shocked chondrites were apparently not totally degassed of ⁴⁰Ar by the event, but retained from ~ 2 to ~45% of their ⁴⁰Ar. When calculated values of the diffusion parameter, $\text{D}\text{a}{}^2$, for Ar are examined in Arrhenius plots, they show two distinct linear relationships, which apparently correspond to the degassing of different mineral phases with distinct $\text{K}\text{Ca}$ ratios and different average temperatures for Ar release. The experimentally determined values of $\text{D}\text{a}{}^2$ for the high temperature phase of several severely shocked chondrites are ~10^?7 to 10^?5sec^?1 for their determined shock-heating temperatures of ~950°C to ~ 1200°C. The inferred reheating temperatures, $\text{D}\text{a}{}^2$ values, and fraction of ⁴⁰Ar loss during the reheating event for these seven chondrites suggest post-shock cooling rates and burial depth of ~ 10^?2 10^?4°C/sec and ~0.5–2m, respectively. For three chondrites these cooling rates agree with those determined from Ni diffusion in metal grains: for five chondrites the cooling rates derived from ⁴⁰Ar and Ni disagree by a factor of ~10⁵. It is suggested that five of these severely shocked chondrites were part of large ejecta blankets containing hot material and cold clasts with a distribution of sizes and that the cooling rate of this ejecta appreciably decreased as a function of time.  相似文献   

K–Ar ages of meteorites: Clues to parent-body thermal histories     

Donald D. Bogard 《Chemie der Erde / Geochemistry》2011,71(3):207-226

Whereas most radiometric chronometers give formation ages of individual meteorites >4.5 Ga ago, the K–Ar chronometer rarely gives times of meteorite formation. Instead, K–Ar ages obtained by the ³⁹Ar–⁴⁰Ar technique span the entire age of the solar system and typically measure the diverse thermal histories of meteorites or their parent objects, as produced by internal parent body metamorphism or impact heating. This paper briefly explains the Ar–Ar dating technique. It then reviews Ar–Ar ages of several different types of meteorites, representing at least 16 different parent bodies, and discusses the likely thermal histories these ages represent. Ar–Ar ages of ordinary (H, L, and LL) chondrites, R chondrites, and enstatite meteorites yield cooling times following internal parent body metamorphism extending over ∼200 Ma after parent body formation, consistent with parent bodies of ∼100 km diameter. For a suite of H-chondrites, Ar–Ar and U–Pb ages anti-correlate with the degree of metamorphism, consistent with increasing metamorphic temperatures and longer cooling times at greater depths within the parent body. In contrast, acapulcoites–lodranites, although metamorphosed to higher temperatures than chondrites, give Ar–Ar ages which cluster tightly at ∼4.51 Ga. Ar–Ar ages of silicate from IAB iron meteorites give a continual distribution across ∼4.53–4.32 Ga, whereas silicate from IIE iron meteorites give Ar–Ar ages of either ∼4.5 Ga or ∼3.7 Ga. Both of these parent bodies suffered early, intense collisional heating and mixing. Comparison of Ar–Ar and I–Xe ages for silicate from three other iron meteorites also suggests very early collisional heating and mixing. Most mesosiderites show Ar–Ar ages of ∼3.9 Ga, and their significantly sloped age spectra and Ar diffusion properties, as well as Ni diffusion profiles in metal, indicate very deep burial after collisional mixing and cooling at a very slow rate of ∼0.2 °C/Ma. Ar–Ar ages of a large number of brecciated eucrites range over ∼3.4–4.1 Ga, similar to ages of many lunar highland rocks. These ages on both bodies were reset by large impact heating events, possibly initiated by movements of the giant planets. Many impact-heated chondrites show impact-reset Ar–Ar ages of either >3.5 Ga or <1.0 Ga, and generally only chondrites show these younger ages. The younger ages may represent orbital evolution times in the asteroid belt prior to ejection into Earth-crossing orbits. Among martian meteorites, Ar–Ar ages of nakhlites are similar to ages obtained from other radiometric chronometers, but apparent Ar–Ar ages of younger shergottites are almost always older than igneous crystallization ages, because of the presence of excess (parentless) ⁴⁰Ar. This excess ⁴⁰Ar derives from shock-implanted martian atmosphere or from radiogenic ⁴⁰Ar inherited from the melt. Differences between meteorite ages obtained from other chronometers (e.g., I–Xe and U–Pb) and the oldest measured Ar–Ar ages are consistent with previous suggestions that the ⁴⁰K decay parameters in common use are incorrect and that the K–Ar age of a 4500 Ma meteorite should be possibly increased, but by no more than ∼20 Ma.  相似文献   

Sorption of noble gases by solids,with reference to meteorites. I. Magnetite and carbon     

Jongmann Yang  Roy S. Lewis  Edward Anders 《Geochimica et cosmochimica acta》1982,46(6):841-860

To simulate trapping of meteoritic noble gases by solids, 18 samples of Fe₃O₄ were synthesized in a noble gas atmosphere at 350–720 K by the reactions: 3Fe + 4H₂O → Fe₃O₄ + 4H₂ (Ne, Ar, Kr, Xe) 3Fe + 4CO → Fe₃O₃ + 4C + carbides (Xe only) Phases were separated by selective solvents (HgCl₂, HCl). Noble gas contents were analyzed by mass spectrometry, or, in runs where 36 d Xe¹²⁷ tracer was used, by γ-counting. Surface areas, as measured by the BET method, ranged from 1 to 400 m²/g. Isotopic fractionations were below the detection limit of 0.5%/m.u.Sorption of Xe on Fe₃O₄ and C obeys Henry's Law between $\text{1 × 10}{}^{\mathrm{?8}}$ and $\text{4 × 10}{}^{\mathrm{?5}}$ atm, but shows only a slight temperature dependence between 650 and 720 K ($\text{ΔH}{}_{\mathrm{sol}}\text{= ?4 ± 2}\text{kcal/mole}$). The mean distribution coefficient K_Xe is $\text{0.28 ± 0.09}$ cc STP/g atm for Fe₃O₄ and only a factor of $\text{1.2 ± 0.4}$ greater for C; such similarity for two cogenetic phases was predicted by Lewis et al. (1977). Stepped heating and etching experiments show that 20–50% of the total Xe is physically adsorbed and about 20% is trapped in the solid. The rest is chemisorbed with $\text{ΔH}{}_{\mathrm{s}}\text{? ?13}\text{kcal/mole}$. The desorption or exchange half-time for the last two components is >10² yr at room temperature.Etching experiments showed a possible analogy to “Phase $\text{Q}$” in meteorites. A typical carbon + carbide sample, when etched with HNO₃, lost 47% of its Xe but only 0.9% of its mass, corresponding to a ~0.6 Å layer. Though this etchable, surficial gas component was more thermolabile than $\text{Q}$ (release $\text{T}$ below 1000°C, compared to 1200–1600°C), another experiment shows that the proportion of chemisorbed Xe increases upon moderate heating (1 hr at 450°C). Apparently adsorbed gases can become “fixed” to the crystal, by processes not involving volume diffusion (recrystallization, chemical reaction, migration to traps, etc.). Such mechanisms may have acted in the solar nebula, to strengthen the binding of adsorbed gases.Adsorbed atmospheric noble gases are present in all samples, and dominate whenever the noble gas partial pressure in the atmosphere is greater than that in the synthesis. Many of the results of Lancet and Anders (1973) seem to have been dominated by such an atmospheric component; others are suspect for other reasons, whereas still others seem reliable. When the doubtful samples of Lancet and Anders are eliminated or corrected, the fractionation pattern—as in our samples—no longer peaks at Ar, but rises monotonically from Ne to Xe. No clear evidence remains for the strong temperature dependence claimed by these authors.  相似文献   

Volatile elements in chondrites: metamorphism or nebular fractionation?     

H Takahashi  Jacques Gros  H Higuchi  John W Morgans  Edward Anders 《Geochimica et cosmochimica acta》1978,42(12):1859-1869

Three of the most highly metamorphosed meteorites of their respective classes, Shaw (LL7), Karoonda (C5), and Coolidge (C4), were analyzed by radiochemical neutron activation analysis for Ag, Au, Bi, Br, Cd, Cs, Ge, In, Ir, Ni, Os, Pd, Rb, Re, Sb, Se, Te, Tl, U, and Zn. Comparison with data by Lipschutz and coworkers on artificially heated primitive meteorites shows that the natural metamorphism of meteorites cannot have taken place in a system open to volatiles. Shaw, metamorphosed at 1300°C for >10⁶ yr, is less depleted in In, Bi, Ag, Te, Zn, and Tl than Krymka heated at 1000°C for 1 week. Karoonda, metamorphosed at 600°C for many millennia, is less depleted in Bi and Tl than Allende heated at 600°C for 1 week.Data on primordial noble gases also show that the volatile-element patterns of ordinary and carbonaceous chondrites were established by nebular condensation, and changed little if at all during metamorphism. For enstatite chondrites, the evidence is still incomplete, but seems to favor a nebular origin of the volatile pattern.The general constancy of Tl/Rb, Tl/Cs and Tl/U ratios in terrestrial and lunar rocks suggests that loss of volatile metals such as Tl is rare during normal magmatism or metamorphism. Only impact melts show such loss with any frequency.  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   

Noble gases,nitrogen and cosmic ray exposure age of the Sulagiri chondrite     

Ramakant R. Mahajan 《地学前缘(英文版)》2017,8(1):205-210

The Sulagiri meteorite fell in India on 12 September 2008,LL6 chondrite class is the largest among all the Indian meteorites.Isotopic compositions of noble gases(He,Ne,Ar,Kr and Xe) and nitrogen in the Sulagiri meteorite and cosmic ray exposure history are discussed.Low cosmogenic(~(22)Ne/~(21)Ne)_c ratio is consistent with irradiation in a large body.Cosmogenic noble gases indicate that Sulagiri has a 4πcosmic-ray exposure(CRE) age of 27.9 ± 3.4 Ma and is a member of the peak of CRE age distribution of IX chondrites.Radiogenic ~4He and ~(40)Ar concentrations in Sulagiri yields the radiogenic ages as 2.29 and4.56 Ca,indicating the loss of He from the meteorite.Xenon and krypton are mixture of Q and spallogenic components.  相似文献   

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   

I-Xe dating of silicate and troilite from IAB iron meteorites     

Sidney Nemeyer 《Geochimica et cosmochimica acta》1979,43(6):843-860

The IAB iron meteorites may be related to the chondrites: siderophile elements in the metal matrix have chondritic abundances, and the abundant silicate inclusions are chondritic both in mineralogy and in chemical composition. Silicate and troilite (FeS) from IAB irons were analyzed by the I-Xe technique. Four IAB silicate samples gave well-defined I-Xe ages [in millions of years relative to Bjurböle; the monitor error (± 2.5 Myr) is not included]: ?3.7 ± 0.3 for Woodbine, ?0.7 ± 0. 6 for Mundrabilla, +1.4 ± 0.7 for Copiapo, and +2.6 ± 0.6 for Landes. The (¹²⁹Xe/¹³²Xe)_trapped ratios are consistent with previous values for chondrites, with the exception of Landes which has an extraordinary trapped ratio of 3.5 ± 0.2. Both analyses of silicate from Pitts gave anomalous I-Xe patterns.Troilite samples were also analyzed: Pitts troilite gave a complex I-Xe pattern, which suggests an age of +17 Myr; Mundrabilla troilite defined a good I-Xe correlation, which after correction for neutron capture on ¹²⁸Te gave an age of ?10.8 ± 0.7 Myr. Thus, surprisingly, low-melting troilite substantially predates high-melting silicate in Mundrabilla.Abundances of Ga, Ge, and Ni in metal from these meteorites are correlated with I-Xe ages of the silicate; meteorites with older silicates have greater Ni contents. No model easily accounts for this result as well as other properties of IAB irons; nevertheless, these results, taken at face value, overall favor a nebular formation model (e.g. Wasson, 1970, Icarus 12, 407–423). The great age of troilite from Mundrabilla suggests that this troilite formed in a different nebular region from the silicate and metal, and was later mechanically mixed with these other phases.The correlation between the trace elements in the metal and the I-Xe ages of the silicate provides one of the first known instances in which another well-defined meteoritic property correlates with I-Xe ages. In addition, almost all the ¹²⁹Xe in Mundrabilla silicate (etched in acid) was correlated with ¹²⁸Xe. These two results further support the validity of the I-Xe dating method.  相似文献   

Noble gas and oxygen isotope studies of aubrites: A clue to origin and histories     

Yayoi N. Miura  Hiroshi Hidaka  Minoru Kusakabe 《Geochimica et cosmochimica acta》2007,71(1):251-270

Noble gas measurements were performed for nine aubrites: Bishopville, Cumberland Falls, Mayo Belwa, Mount Egerton, Norton County, Peña Blanca Spring, Shallowater, ALHA 78113 and LAP 02233. These data clarify the origins and histories, particularly cosmic-ray exposure and regolith histories, of the aubrites and their parent body(ies). Accurate cosmic-ray exposure ages were obtained using the ⁸¹Kr-Kr method for three meteorites: 52 ± 3, 49 ± 10 and 117 ± 14 Ma for Bishopville, Cumberland Falls and Mayo Belwa, respectively. Mayo Belwa shows the longest cosmic-ray exposure age determined by the ⁸¹Kr-Kr method so far, close to the age of 121 Ma for Norton County. These are the longest ages among stony meteorites. Distribution of cosmic-ray exposure ages of aubrites implies 4-9 break-up events (except anomalous aubrites) on the parent body. Six aubrites show “exposure at the surface” on their parent body(ies): (i) neutron capture ³⁶Ar, ⁸⁰Kr, ⁸²Kr and/or ¹²⁸Xe probably produced on the respective parent body (Bishopville, Cumberland Falls, Mayo Belwa, Peña Blanca Spring, Shallowater and ALHA 78113); and/or (ii) chondritic trapped noble gases, which were likely released from chondritic inclusions preserved in the aubrite hosts (Cumberland Falls, Peña Blanca Spring and ALHA 78113). The concentrations of ¹²⁸Xe from neutron capture on ¹²⁷I vary among four measured specimens of Cumberland Falls (0.5-76 × 10⁻¹⁴ cm³STP/g), but are correlated with those of radiogenic ¹²⁹Xe, implying that the concentrations of (¹²⁸Xe)_n and (¹²⁹Xe)_rad reflect variable abundances of iodine among specimens. The ratios of (¹²⁸Xe)_n/(¹²⁹Xe)_rad obtained in this work are different for Mayo Belwa (0.045), Cumberland Falls (0.015) and Shallowater (0.001), meaning that neutron fluences, radiogenic ¹²⁹Xe retention ages, or both, are different among these aubrites. Shallowater contains abundant trapped Ar, Kr and Xe (2.2 × 10⁻⁷, 9.4 × 10⁻¹⁰ and 2.8 × 10⁻¹⁰ cm³STP/g, respectively) as reported previously (Busemann and Eugster, 2002). Isotopic compositions of Kr and Xe in Shallowater are consistent with those of Q (a primordial noble gas component trapped in chondrites). The Ar/Kr/Xe compositions are somewhat fractionated from Q, favoring lighter elements. Because of the unbrecciated nature of Shallowater, Q-like noble gases are considered to be primordial in origin. Fission Xe is found in Cumberland Falls, Mayo Belwa, Peña Blanca Spring, ALHA 78113 and LAP 02233. The majority of fission Xe is most likely ²⁴⁴Pu-derived, and about 10-20% seems to be ²³⁸U-derived at ¹³⁶Xe. The observed (¹³⁶Xe)_Pu corresponds to 0.019-0.16 ppb of ²⁴⁴Pu, from which the ²⁴⁴Pu/U ratios are calculated as 0.002-0.009. These ratios resemble those of chondrites and other achondrites like eucrites, suggesting that no thermal resetting of the Pu-Xe system occurred after ∼4.5 Ga ago. We also determined oxygen isotopic compositions for four aubrites with chondritic noble gases and a new aubrite LAP 02233. In spite of their chondritic noble gas signatures, oxygen with chondritic isotopic compositions was found only in a specimen of Cumberland Falls (Δ¹⁷O of ∼0.3‰). The other four aubrites and the other two measured specimens of Cumberland Falls are concurrent with the typical range for aubrites.  相似文献   

New data on the abundance of palladium in meteorites     

N Mermelengas  J.R De Laeter  K.J.R Rosman 《Geochimica et cosmochimica acta》1979,43(5):747-753

The concentration of Pd in 7 carbonaceous chondrites, 18 ordinary chondrites, 3 achondrites, 29 iron meteorites and other samples has been determined by stable isotope dilution using solid source mass spectrometry. The Cl chondrite Orgueil gives a ‘cosmic’ abundance for Pd of 1.5 (Si = 10⁶ atoms), in good agreement with the currently accepted value.The concentration of Pd shows little variation among the carbonaceous chondrites, but in ordinary chondrites decreases from the H to L to LL groups. Pd in achondrites is approx 100 times lower than in chondrites. Data for iron meteorites plot around the ‘cosmic’ $\text{Pd}\text{Ni}$ ratio; however the Pd data falls into distinct groups, corresponding to the chemical group classification. These results support the hypothesis that at least two fractionation processes have occurred during the formation of iron meteorites.  相似文献   

Origin of isotopically light nitrogen in meteorites     

A. B. Verchovsky 《Geochemistry International》2017,55(11):957-970

Bulk meteorite samples of various chemical classes and petrologic types (mainly carbonaceous chondrites) were systematically investigated by the stepped combustion method with the simultaneous isotopic analysis of carbon, nitrogen, and noble gases. A correlation was revealed between planetary noble gases associating with the Q phase and isotopically light nitrogen (δ¹⁵N up to –150‰). The analysis of this correlation showed that the isotopically light nitrogen (ILN) is carried by Q. In most meteorites, isotopically heavy nitrogen (IHN) of organic compounds (macromolecular material) is dominant. The ILN of presolar grains (diamond and SiC) and Q can be detected after separation from dominant IHN. Such a separation of nitrogen from Q and macromolecular material occurs under natural conditions and during laboratory stepped combustion owing to Q shielding from direct contact with oxygen, which results in Q oxidation at temperatures higher than the temperatures of the release of most IHN. There are arguments that ILN released at high temperature cannot be related to nanodiamond and SiC. The separation effect allowed us to constrain the contents of noble gases in Q, assuming that this phase is carbon-dominated. The directly measured ³⁶Ar/C and ¹³²Xe/C ratios in ILN-rich temperature fractions are up to 0.1 and 1 × 10^–4 cm³/g, respectively. These are only lower constraints on the contents. The analysis of the obtained data on the three-isotope diagram δ¹⁵N–³⁶Ar/¹⁴N showed that Q noble gases were lost to a large extent from most meteorites during the metamorphism of their parent bodies. Hence, the initial contents of noble gases in Q could be more than an order of magnitude higher than those directly measured. Compared with other carbon phases, Q was predominantly transformed to diamond in ureilites affected by shock metamorphism. The analysis of their Ar–N systematics showed that, similar to carbonaceous chondrites, noble gases were lost from Q probably before its transformation to diamond.  相似文献   

The abundances of titanium,zirconium and hafnium in stony meteorites     

Masako Shima 《Geochimica et cosmochimica acta》1979,43(3):353-362

The concentrations of Ti, Zr and Hf have been determined, by a stable isotope dilution method, in 27 chondrites, seven achondrites and standard rock samples BCR-1 and W-1.Among all chondrites investigated, enstatite chondrite Abee is lowest in Ti atomic ratio compared with Si while all carbonaceous chondrites show higher values. The Zr contents are higher in CII and CIII chondrites, relative to the other groups of chondrites. There is a clustering of Ti and Zr within each group. The $\text{Zr}\text{Hf}$ ratios in CII, CIII. E and H chondrites are essentially the same, while that in the CI chondrite is lower and in L, LL and unequilibrated chondrites are higher.The concentrations of Ti, Zr, Hf and $\text{Ti}\text{Zr}$, $\text{Zr}\text{Hf}$ ratios in achondrites are variable, even among members of the same group.Based on these results, condensation models for these elements are discussed. The variable results for Ti, Zr and Hf in achondrites may be due to the reheating recrystallization and metamorphic processes.‘Cosmic atomic abundances’ of Ti, Zr and Hf are calculated as 2470, 11.2 and 0.185. respectively for Si = 10⁶ atoms.  相似文献