The effect of CO ratio on the condensation of planetary material     

John W. Larimer 《Geochimica et cosmochimica acta》1975,39(3):389-392

The condensation temperatures of refractory silicates and oxides in a gas of cosmic composition are strongly dependent on the $\text{C}\text{O}$ ratio. As the ratio increases from 0.4 to 0.9 (solar ~ cosmic ~ 0.6), condensation temperatures of compounds such as A1₂O₃, Ca₂Al₂SiO₇, MgAl₂O₄, Mg₂SiO₄ and MgSiO₃ decrease by 50–100°. As $\text{C}\text{O}$ increases from 0.9 to 1.0, these temperatures drop an additional 300–400°. Other chemical differences result when $\text{C}\text{O}\text{\$}\text{?}\text{0.9}$ include: a new suite of high temperature minerals appears (graphite, CaS, Fe₃C, SiC and TiN); the reaction CO + 3H₂ → CH₄ + H₂O proceeds to the right at higher temperatures; and iron, whose condensation temperature is unaffected, condenses at higher temperatures than any silicate or oxide.  相似文献   

Silicate inclusions in group IAB irons and a relation to the anomalous stones Winona and Mt Morris (Wis)     

Richard W Bild 《Geochimica et cosmochimica acta》1977,41(10):1439-1456

Silicates are found in many group IAB irons; in some cases as abundant angular cm-sized inclusions and in other cases as smaller fragments or single grains in troilite or graphite nodules. The mineralogy of the silicates is chondritic—olivine, pyroxene, albitic plagioclase—as is the bulk composition. The degree of oxidation of the olivine and pyroxene is intermediate between E and H chondrites (Fa 1–8, Fs 4–9). IAB inclusions have ages of about 4.5 Gyr, I¹²⁹-Xe¹²⁹ formation intervals in the ranges of chondrites and contain planetary-type rare gases.Samples of San Cristobal, Campo del Cielo, Mundrabilla and Woodbine were examined by microprobe and bulk inclusions from Campo del Cielo, Copiapo, Landes and Woodbine were analyzed by instrumental and radiochemical neutron activation analysis. Nonvolatile lithophilic and siderophih'c elements in Copiapo, Landes and Woodbine have approximately chondritic abundances. The chondritic level of lithophiles indicates the inclusions have not undergone igneous differentiation while the chondritic levels of siderophiles is evidence the metal is native to the inclusions and not matrix metal injected into the silicates. The two Campo del Cielo inclusions analyzed have roughly chondritic abundances of lithophiles but have fractionated rare earth patterns and widely varying amounts and abundances (relative to Ni) of siderophiles. These inclusions appear to have experienced some partial melting. Siderophile ratios for the inclusions have some differences when compared to matrix metal. One Campo del Cielo inclusion contains kamacite (5.5% Ni) with over 1000 μg Ge.Three-isotope O analyses by Clayton and coworkers of parts of the same or neighboring inclusions to those analyzed chemically place the inclusions slightly below the terrestrial fractionation line of clayton et al. (1976) and rule out the possibility of the inclusions being trapped fragments of one of the ordinary chondrite groups.The IAB silicates formed probably in a similar manner as chondrite groups but in a different region of the nebula and they record the O₂ fugacity and O isotopic composition of that location. They later became trapped in the metal-rich matrix probably as the result of collisions producing the breccialike texture. The relationship of the silicates to the kamacite-taenite structure of the metal requires that the metal-silicate mix have been heated to over 1000 K for an extended period.Two anomalous stony meteorites, Winona and Mt. Morris (Wis), are similar to IAB inclusions in mineralogy, bulk composition, $\text{FeO}\text{(FeO + Mg)}$ ratio of the silicates, and chromite composition and are possibly related to the IAB silicates. Winona also has an age of 4.6 Gyr and contains planetary-type rare gases. Microprobe data are reported for the major minerals of these anomalous meteorites. Although attempts to detect IAB levels of Ge in the metal phases were not successful, the weight of the evidence favors a relationship between these meteorites and IAB  相似文献   

Can enstatite meteorites form from a nebula of solar composition?     

J.M. Herndon  H.E. Suess 《Geochimica et cosmochimica acta》1976,40(4):395-399

Doubts have been expressed as to whether solar matter is sufficiently reducing to explain the minerals occurring in the enstatite chondrites and in the enstatite achondrites. Thermodynamic calculations on the stabilities of TiN, Si₂N₂O, CaS and silicon-bearing iron metal show that these substances can form under equilibrium conditions from a nebula of solar composition provided that the total pressure exceeds ~ 1 atm and that thermodynamic equilibria are frozen in at near-formation temperatures.  相似文献   

The mineral chemistry and origin of inclusion matrix and meteorite matrix in the Allende CV3 chondrite     

Alan S. Kornacki  John A. Wood 《Geochimica et cosmochimica acta》1984,48(8):1663-1676

The two textural varieties of olivine-rich Allende inclusions (rimmed and unrimmed olivine aggregates) consist primarily of a porous, fine-grained mafic constituent (inclusion matrix) that differs from the opaque meteorite matrix of CV3 chondrites by being relatively depleted in sulfides, metal grains, and (perhaps) carbonaceous material. Olivine is the most abundant mineral in Allende inclusion matrix; clinopyroxene, nepheline, sodalite, and Ti-Al-pyroxene occur in lesser amounts. Olivine in unrimmed olivine aggregates (Type 1A inclusions) is ferrous and has a narrow compositional range (Fo_50–65). Olivine in rimmed olivine aggregates (Type 1B inclusions) is, on average, more magnesian, with a wider compositional range (Fo_53–96). Olivine grains in the granular rims of Type 1B inclusions are zoned, with magnesian cores (Fo_>80) and ferrous rinds (Fo_<70). Ferrous olivines (Fo_<65) in both varieties of inclusions commonly contain significant amounts of Al₂O₃ (as much as ~0.7 wt%), CaO (as much as ~0.4 wt%), and TiO₂ (as much as ~0.2 wt%), refractory elements that probably occur in submicroscopic inclusions of Ca,Al,Ti-rich glass (rather than in the olivine crystal structure). Defocussed beam analyses of Allende matrix materials demonstrate that: (1) inclusion matrix in Type 1A inclusions is more enriched in olivine and FeO than inclusion matrix in the cores of Type 1B inclusions; (2) opaque matrix materials are depleted in feldspathoids and enriched in sulfides and metal grains relative to inclusion matrix; (3) the bulk compositions of Type 1A and Type 1B inclusions overlap; and (4) excluding sulfides and metal, the bulk compositions of Allende matrix materials cluster in a complementary pattern around the bulk composition of C1 chondrites.Inclusion matrix and meteorite matrix in Allende and other CV3 chondrites are probably relatively primitive nebular material, but a careful evaluation of the equilibrium condensation model suggests that these matrix materials do not consist of crystalline phases that formed under equilibrium conditions in a relatively cool gas of solar composition. Allende inclusion matrix is interpreted as an aggregate of condensates that formed under relatively oxidizing, non-equilibrium conditions from supercooled, supersaturated vapors produced during the vaporization of interstellar dust by aerodynamic drag heating in the solar nebula; CV3 meteorite matrix contains, in addition, a proportion of interstellar material that was heated (but not vaporized) in the nebula. Granular olivine in rimmed olivine aggregates may have formed during the recrystallization and incipient melting of aggregates of inclusion matrix in the nebula. The mineral chemistry of matrix olivine in Allende seems to have been established by three different processes: non-equilibrium vapor → solid condensation; recrystallization and partial melting in the nebula; and $\text{Fe}\text{Mg}$ equilibration (without textural homogenization) in the meteorite parent body.  相似文献   

Elemental fractionations among enstatite chondrites     

Philip A Baedecker  John T Wasson 《Geochimica et cosmochimica acta》1975,39(5):735-765

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Presolar diamond, silicon carbide, and graphite in carbonaceous chondrites: implications for thermal processing in the solar nebula     

Gary R. Huss  Alex P. Meshik  C.M. Hohenberg 《Geochimica et cosmochimica acta》2003,67(24):4823-4848

We have determined abundances of presolar diamond, silicon carbide, graphite, and Xe-P1 (Q-Xe) in eight carbonaceous chondrites by measuring the abundances of noble gas tracers in acid residues. The meteorites studied were Murchison (CM2), Murray (CM2), Renazzo (CR2), ALHA77307 (CO3.0), Colony (CO3.0), Mokoia (CV3_ox), Axtell (CV3_ox), and Acfer 214 (CH). These data and data obtained previously by Huss and Lewis (1995) provide the first reasonably comprehensive database of presolar-grain abundances in carbonaceous chondrites. Evidence is presented for a currently unrecognized Ne-E(H) carrier in CI and CM2 chondrites.After accounting for parent-body metamorphism, abundances and characteristics of presolar components still show large variations across the classes of carbonaceous chondrites. These variations correlate with the bulk compositions of the host meteorites and imply that the same thermal processing that was responsible for generating the compositional differences between the various chondrite groups also modified the initial presolar-grain assemblages. The CI chondrites and CM2 matrix have the least fractionated bulk compositions relative to the sun and the highest abundances of most types of presolar material, particularly the most fragile types, and thus are probably most representative of the material inherited from the sun's parent molecular cloud. The other classes can be understood as the products of various degrees of heating of bulk molecular cloud material in the solar nebula, removing the volatile elements and destroying the most fragile presolar components, followed by chondrule formation, metal-silicate fractionation in some cases, further nebula processing in some cases, accretion, and parent body processing. If the bulk compositions and the characteristics of the presolar-grain assemblages in various chondrite classes reflect the same processes, as seems likely, then differential condensation from a nebula of solar composition is ruled out as the mechanism for producing the chondrite classes. Presolar grains would have been destroyed if the nebula had been completely vaporized. Our analysis shows that carbonaceous chondrites reflect all stages of nebular processing and thus are no more closely related to one another than they are to ordinary and enstatite chondrites.  相似文献   

The metal content of the eucrite parent body: constraints from the partitioning behavior of tungsten     

Horton E. Newsom  Michael J. Drake 《Geochimica et cosmochimica acta》1982,46(12):2483-2489

The solid metal/silicate melt partition coefficient for W has been determined experimentally to have a value of 25 ± 5 at 1190°C and an oxygen fugacity of 10^?13.4, the temperature and oxygen fugacity conditions at which eucritic basalts formed. Given this partition coefficient, scenarios for the metal content and evolution of the eucrite parent body (EPB) are constructed to explain the reduction by a factor of 30, relative to the chondrites, of the $\text{W}\text{La}$ ratio in the eucrites.A possible model for the early geologic history of the EPB begins with accretion of a parent body, chondritic in composition with respect to nonvolatile siderophile and lithophile elements. The solid metal content was between 2% and 10%, which is within the range observed in the ordinary chondrites. Subsequent heating of the EPB caused the metal phase to separate and become isolated from the silicate phases before the degree of partial melting of the silicates reached 4% to 5%. Equilibrium partitioning of most of the W into the solid metal phase at low degrees of partial melting reduced the $\text{W}\text{La}$ ratio in the remaining silicates. Continued partial melting of the silicates generated primary eucritic magmas which recorded the reduced $\text{W}\text{La}$ ratio.  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   

Interstellar organic matter in meteorites     

Jongmann Yang  Samuel Epstein 《Geochimica et cosmochimica acta》1983,47(12):2199-2216

Hydrogen which is highly enriched in deuterium is present in organic matter in a variety of meteorites including non-carbonaceous chondrites. The concentrations of this hydrogen are quite large. For example Renazzo contains 140 μmoles/g of the 10,000‰ δD hydrogen. The $\text{D}\text{H}$ ratios of hydrogen in the organic matter vary from 8 × 10^?5 to 170 × 10^?5 (δD ranges from ? 500‰ to 10,000‰) as compared to 16 × 10^?5 for terrestrial hydrogen and 2 × 10^?5 for cosmic hydrogen. The majority of the unequilibrated primitive meteorites contain hydrogen whose $\text{D}\text{H}$ ratios are greater than 30 × 10^?5. If the $\text{D}\text{H}$ ratios in these compounds were due to enrichment relative to cosmic hydrogen by isotope exchange reactions, it would require that these reactions take place below 150 K. In addition the organic compounds having $\text{D}\text{H}$ ratios above 50 × 10^?5 would require temperatures of formation of < 120 K. These types of deuterium enrichments must take place by ion-molecule reactions in interstellar clouds where both ionization and low temperatures exist. Astronomically observed $\text{D}\text{H}$ ratios in organic compounds in interstellar clouds are typically 180 × 10^?5 and range between about 40 × 10^?5 and 5000 × 10^?5. The $\text{D}\text{H}$ values we have determined are the lower limits for the organic compounds derived from interstellar molecules because all processes subsequent to their formation, including terrestrial contamination, decrease their $\text{D}\text{H}$ ratios.In contrast, the $\text{D}\text{H}$ ratios of hydrogen associated with hydrated silicates are relatively uniform for the meteorites we have analyzed with an average value of 14 × 10^?5; very similar to the terrestrial value. These phyllosilicates values suggest equilibration of H₂O with H₂ in the solar nebula at temperatures of about 200 K and higher.The ${}^{13}\text{C}{}^{12}\text{C}$ ratios of organic matter, irrespective its $\text{D}\text{H}$ ratio, lie well within those observed for the earth. If organic matter originated in the interstellar medium, our data would indicate that the ${}^{13}\text{C}{}^{12}\text{C}$ ratio of interstellar carbon five billion years ago was similar to the present terrestrial value.Our findings suggest that other interstellar material, representing various inputs from various stars, in addition to the organic matter is preserved and is present in the meteorites which contain the high $\text{D}\text{H}$ ratios. We feel that some elements existing in trace quantities which possess isotopic anomalies in the meteorites may very well be such materials.  相似文献   

Oxygen isotopic compositions of chondrules: Implications for evolution of oxygen isotopic reservoirs in the inner solar nebula   总被引：1，自引：0，他引：1  

Alexander N. Krot  Hisayoshi Yurimoto  Kevin D. McKeegan  Laurie Leshin  Marc Chaussidon  Guy Libourel  Miwa Yoshitake  Gary R. Huss  Yunbin Guan  Brigitte Zanda 《Chemie der Erde / Geochemistry》2006,66(4):249-276

We review the oxygen isotopic compositions of minerals in chondrules and compound objects composed of a chondrule and a refractory inclusion, and bulk oxygen isotopic compositions of chondrules in unequilibrated ordinary, carbonaceous, enstatite, and Kakangari-like chondrites, focusing on data acquired using secondary ion mass-spectrometry and laser fluorination coupled with mass-spectrometry over the last decade. Most ferromagnesian chondrules from primitive (unmetamorphosed) chondrites are isotopically uniform (within 3–4‰ in Δ¹⁷O) and depleted in ¹⁶O (Δ¹⁷O>−7‰) relative to amoeboid olivine aggregates (AOAs) and most calcium–aluminum-rich inclusions (CAIs) (Δ¹⁷O<−20‰), suggesting that these classes of objects formed in isotopically distinct gaseous reservoirs, ¹⁶O-poor and ¹⁶O-rich, respectively. Chondrules uniformly enriched in ¹⁶O (Δ¹⁷O<−15‰) are exceptionally rare and have been reported only in CH chondrites. Oxygen isotopic heterogeneity in chondrules is mainly due to the presence of relict grains. These appear to consist of chondrules of earlier generations and rare refractory inclusions; with rare exceptions, the relict grains are ¹⁶O-enriched relative to chondrule phenocrysts and mesostasis. Within a chondrite group, the magnesium-rich (Type I) chondrules tend to be ¹⁶O-enriched relative to the ferrous (Type II) chondrules. Aluminum-rich chondrules in ordinary, enstatite, CR, and CV chondrites are generally ¹⁶O-enriched relative to ferromagnesian chondrules. No systematic differences in oxygen isotopic compositions have been found among these chondrule types in CB chondrites. Aluminum-rich chondrules in carbonaceous chondrites often contain relict refractory inclusions. Aluminum-rich chondrules with relict CAIs have heterogeneous oxygen isotopic compositions (Δ¹⁷O ranges from −20‰ to 0‰). Aluminum-rich chondrules without relict CAIs are isotopically uniform and have oxygen isotopic compositions similar to, or approaching, those of ferromagnesian chondrules. Phenocrysts and mesostases of the CAI-bearing chondrules show no clear evidence for ¹⁶O-enrichment compared to the CAI-free chondrules. Spinel, hibonite, and forsterite of the relict refractory inclusions largely retained their original oxygen isotopic compositions. In contrast, plagioclase and melilite of the relict CAIs experienced melting and ¹⁶O-depletion to various degrees, probably due to isotopic exchange with an ¹⁶O-poor nebular gas. Several igneous CAIs experienced isotopic exchange with an ¹⁶O-poor nebular gas during late-stage remelting in the chondrule-forming region. On a three-isotope diagram, bulk oxygen isotopic compositions of most chondrules in ordinary, enstatite, and carbonaceous chondrites plot above, along, and below the terrestrial fractionation line, respectively. Bulk oxygen isotopic compositions of chondrules in altered and/or metamorphosed chondrites show evidence for mass-dependent fractionation, reflecting either interaction with a gaseous/fluid reservoir on parent asteroids or open-system thermal metamorphism. Bulk oxygen isotopic compositions of chondrules and oxygen isotopic compositions of individual minerals in chondrules and refractory inclusions from primitive chondrites plot along a common line of slope of 1, suggesting that only two major reservoirs (gas and solids) are needed to explain the observed variations. However, there is no requirement that each had a permanently fixed isotopic composition. The absolute (²⁰⁷Pb–²⁰⁶Pb) and relative (²⁷Al–²⁶Mg) chronologies of CAIs and chondrules and the differences in oxygen isotopic compositions of most chondrules (¹⁶O-poor) and most refractory inclusions (¹⁶O-rich) can be interpreted in terms of isotopic self-shielding during UV photolysis of CO in the initially ¹⁶O-rich (Δ¹⁷O−25‰) parent molecular cloud or protoplanetary disk. According to these models, the UV photolysis preferentially dissociates C¹⁷O and C¹⁸O in the parent molecular cloud and in the peripheral zones of the protoplanetary disk. If this process occurs in the stability field of water ice, the released atomic ¹⁷O and ¹⁸O are incorporated into water ice, while the residual CO gas becomes enriched in ¹⁶O. During the earliest stages of evolution of the protoplanetary disk, the inner solar nebula had a solar H₂O/CO ratio and was ¹⁶O-rich. During this time, AOAs and the ¹⁶O-rich CAIs and chondrules formed. Subsequently, the inner solar nebula became H₂O- and ¹⁶O-depleted, because ice-rich dust particles, which were depleted in ¹⁶O, agglomerated outside the snowline (5 AU), drifted rapidly towards the Sun and evaporated. During this time, which may have lasted for 3 Myr, most chondrules and the ¹⁶O-depleted igneous CAIs formed. We infer that most chondrules formed from isotopically heterogeneous, but ¹⁶O-depleted precursors, and experienced isotopic exchange with an ¹⁶O-poor nebular gas during melting. Although the relative roles of the chondrule precursor materials and gas–melt isotopic exchange in establishing oxygen isotopic compositions of chondrules have not been quantified yet, mineralogical, chemical, and isotopic evidence indicate that Type I chondrules may have formed in chemical and isotopic equilibrium with nebular gas of variable isotopic composition. Whether these variations were spatial or temporal are not known yet.  相似文献   

$\text{Ca}\text{Al}$ ratio and composition of the Earth's upper mantle     

H Palme  K.G Nickel 《Geochimica et cosmochimica acta》1985,49(10):2123-2132

Undifferentiated meteorites (chondrites) have the same relative abundances of refractory lithophile elements (Ca, Al, Ti, Sc, REE, etc.), despite variable absolute concentrations. The reasonable assumption of chondritic ratios among refractory elements in the bulk Earth is used to constrain the chemical composition of the upper mantle in the following way: Correlations of the compatible refractory elements Ca, Al, Ti, Sc and Yb with MgO are worldwide very similar in suites of spinel-lherzolite xenoliths from basaltic rocks. Such suites represent upper mantle material depleted to differing degrees by extraction of partial melts. From these refractory elements vs. MgO correlations, ratios of pairs of refractory elements were calculated at various MgO contents. Chondritic $\text{Al}\text{Ti}$ and $\text{Sc}\text{Ti}$ ratios were only obtained for MgO contents below 36%. A chrondritic $\text{Sc}\text{Yb}$ ratio requires an MgO content above 35%. We therefore accept 35.5% as the most reasonable MgO content of undepleted upper mantle. This MgO content is slightly below the spinel-lherzolite with the lowest measured MgO content (36.22%). The corresponding Al₂O₃ content of 4.75% is higher than in previous estimates of upper mantle composition. The concentrations of other elements were obtained from similar correlations at a MgO content of 35.5%. The resulting present upper mantle composition is enriched in refractory elements by a factor of 1.49 relative to Si and Cl and by a factor of 1.12 for Mg relative to Si and Cl. These enrichments are in the same range as those for the Vigarano type carbonaceous chondrites. The Mg/Mg + Fe ratio of 89 is slightly lower than previous estimates.The $\text{Ca}\text{Al}$ ratio in spinel lherzolite suites is, however, uniformly higher worldwide than the chondritic ratio by about 15%. Orogenic peridotites as well as komatiites appear to have similar non-chondritic $\text{Ca}\text{Al}$ ratios. It is therefore suggested that this non-chondritic $\text{Ca}\text{Al}$ ratio is a characteristic of the upper mantle, possibly since the Archean. A minor fractionation of about 4% of garnet in an early, global melting event (deep magma ocean?) is presented as the most likely cause for the high $\text{Ca}\text{Al}\text{-}\text{ratio}$. In this case the addition of 4% of such a garnet component to the undepleted present upper mantle would be required to obtain the composition of the primordial upper mantle. The $\text{Ca}\text{Al}\text{-}\text{ratio}$ of this primordial mantle would be 15% higher than that of the undepleted present upper mantle, resulting in an enrichment of refractory elements of 1.70 ($\text{Al}\text{Si}$ relative to Cl) for the primordial upper mantle.  相似文献   

Unequilibrated ordinary chondrites: A tentative subclassification based on volatile-element content     

Edward Anders  M.G. Zadnik 《Geochimica et cosmochimica acta》1985,49(5):1281-1291

For unequilibrated ordinary chondrites (= UOC), two measures of primitiveness are available: volatile content, in principle reflecting accretion conditions from the solar nebula, and metamorphism, reflecting reheating in the parent bodies. These two measures do not always correlate, and we have therefore developed a tentative classification scheme based on volatile content that complements the Searset al. (1980) scheme based on metamorphism. Like the latter, it subdivides type 3 chondrites on a scale of 3.0 to 3.9; the notation 3.4/0 indicates a meteorite that is subtype 3.4 according to metamorphism and 3.0 according to volatile content.The classification is based mainly on C and Xe—two elements that are little affected by shock-induced reheating—and to a lesser extent on Ar³⁶,Bi,In, and Tl. Of 22 meteorites considered, the majority have concordant classifications (±0.2) on the two scales. However, 5 meteorites are richer in volatiles than their metamorphic grade indicates: Sharps 3.4/0, ALHA 77011 3.5/0, Ngawi 3.6/3, ALHA 77299 3.7/4, and Mezö-Madaras 3.7/3. It remains to be seen whether these differences indeed denote a more primitive nature.Some new clues to the formation of chondrites may eventually come from Xe and C. Their concentrations in UOC's vary by more than 5×, but the $\text{Xe}\text{C}$ ratio remains nearly constant at 3.4 × 10^?3 of the solar-system ratio. Even the ratios for other chondrite classes differ only slightly from that for UOC's, e.g., C3O (1.5×) and E3,4 (0.4×). Either the 4 factors determining this ratio (T, t, P, and internal surface area of the carbon) varied in complementary fashion, or—more probably—they varied only slightly in the entire source region of chondrites.  相似文献   

Experimental investigation of the partitioning of phosphorus between metal and silicate phases: implications for the Earth,Moon and Eucrite Parent Body     

Horton E. Newsom  Michael J. Drake 《Geochimica et cosmochimica acta》1983,47(1):93-100

The solid metal/silicate melt partition coefficient for P, D(P), has been determined experimentally at 1190°C and 1300°C. The dependence of the partition coefficient on oxygen fugacity has been investigated, and is consistent with a valence state of 5 for P in the silicate melt. The experimental partition coefficients are given by: $\text{log D(P) = ?1.21 log ?O}{}_2\text{? 15.95 at 1190°C}$$\text{log D(P) = ?1.53 log ?O}{}_2\text{? 17.73 at 1300°C}$The experimentally determined partition coefficients may be used to interpret the low $\text{P}\text{La}$ ratios of the Earth, Moon and eucrites relative to C1 chondrites. The low $\text{P}\text{La}$ ratios in the eucrites may be explained by partitioning of P into 5% to 25% of a sulfur-bearing metallic liquid assuming equilibration and separation of the liquid metal from the silicates at low degrees of partial melting of the silicates. The low $\text{W}\text{La}$ ratios in the eucrites compared to C1 chondrites require the separation of an additional 2% to 10% solid metal.The lowering of both $\text{P}\text{La}$ and $\text{W}\text{La}$ ratios in the Moon may be explained by partitioning of P and W into metal during formation of a small core by separation of liquid metal from silicate at low degrees of partial melting of the silicates. The $\text{W}\text{La}$ ratios in the Earth and Moon are virtually indistinguishable, while $\text{P}\text{La}$ ratios differ by a factor of two. The concentrations of FeO also appear to be different. These observations are difficult to reconcile with the hypothesis of a terrestrial origin of the Moon following formation of the Earth's core, but are consistent with independent formation of the Earth and Moon.  相似文献   

Electron microprobe study of a ‘mysterite’-bearing inclusion from the Krymka LL-chondrite     

Lawrence Grossman  John M. Allen  Glenn J. MacPherson 《Geochimica et cosmochimica acta》1980,44(2):211-216

The black inclusion from the Krymka LL3 chondrite previously found to contain ‘mysterite’ by Lewiset al. (1979) belongs to a hitherto unknown class of carbonaceous chondrites. Its olivine and pyroxene compositions. Fo 97–99 and En 96, respectively, are characteristic of carbonaceous chondrites and its plagioclase composition. An 100, is characteristic of C3's. It contains a peculiar group of Co-, Cr-rich metal grains whose compositions are similar, but not identical, to those in C2 chondrites and which also bear some similarities to those in Renazzo. Its weight ratios of total $\text{Fe}\text{SiO}{}_2$ and $\text{solSiO}{}_2\text{MgO}$ are 0.74 and 1.43, respectively, and its atomic ratio of $\text{Si}\text{Al}$ is 10.7, exactly the same as in carbonaceous chondrites. Its bulk chemical composition is very close to that of the Murchison C2 chondrite. The association of mysterite with a special type of carbonaceous chondrite material suggests that mysterite formed by low-temperature condensation in a different region of the nebula from other carbonaceous chondrites.  相似文献   

Chemical fractionations in meteorites—IX. C3 chondrites     

Edward Anders  Hideo Higuchi  R. Ganapathy  John W. Morgan 《Geochimica et cosmochimica acta》1976,40(9):1131-1139

Four C3V chondrites (Grosnaja, Kaba, Mokoia, Vigarano) and three C3O chondrites (Felix, Kainsaz, and Lancé) were analyzed by radiochemical neutron activation for 17 trace elements. Both classes show a typical chondritic step pattern, reflecting loss of volatiles during chondrule formation. Elements condensing above 1300 K (U, Re, Ir, Ni) are present in essentially Cl chondrite proportions, while moderately volatile elements condensing between 1300 K and 800 K (Ge, Rb, Ag) are depleted by a factor of 0.44. However, elements condensing below 700 K (S, Cs, Bi, Tl, Br, Se, Te, In, Cd) are depleted to a still greater degree, and more so in the Ornans subclass (factor of 0.24, except Cd 0.007) than in the Vigarano subclass (factor of 0.29). This additional depletion may be due to a slight (less than 3-fold) dust-gas fractionation, by settling of dust to the median plane of the solar nebula. Among other chondrite classes, ordinary chondrites show a similar depletion, but C2 chondrites do not. Possibly the undepleted meteorites formed in one of the convection zones of the nebula predicted by Cameron and Pine, whereas the depleted meteorites formed in a quiescent region.The condensation of chalocophile elements as a function of H₂S partial pressure is discussed, in an attempt to explain the drastic difference in Cd abundance between the two subclasses. It appears that the $\text{H}{}_2\text{S}\text{H}{}_2$ ratio is the key variable. C3O's seem to have condensed in a region where enough metallic Fe was present to buffer the H₂S pressure, while C3V's condensed in a more oxidized region, where H₂S was in excess. Accretion temperatures, for an assumed nebular pressure of 10^?5 atm, were between 415 and 430 K for C3O's and less than 440 K for C3V's.Two slightly volatile elements, Sb and Au, show variable depletion, presumably reflecting variable loss during chondrule formation. Indeed, their depletion correlates with the abundance of iron-poor olivine, a measure of the peak temperature and time during chondrule formation.  相似文献   

Amoeboid olivine aggregates and related objects in carbonaceous chondrites: records of nebular and asteroid processes     

Alexander N. Krot  Michail I. Petaev  Shoichi Itoh  Timothy J. Fagan  Hisayoshi Yurimoto  Michael K. Weisberg  Matsumi Komatsu  Klaus Keil 《Chemie der Erde / Geochemistry》2004,64(3):185-239

Amoeboid olivine aggregates (AOAs) are the most common type of refractory inclusions in CM, CR, CH, CV, CO, and ungrouped carbonaceous chondrites Acfer 094 and Adelaide; only one AOA was found in the CB_b chondrite Hammadah al Hamra 237 and none were observed in the CB_a chondrites Bencubbin, Gujba, and Weatherford. In primitive (unaltered and unmetamorphosed) carbonaceous chondrites, AOAs consist of forsterite (Fa_<2), Fe, Ni-metal (5-12 wt% Ni), and Ca, Al-rich inclusions (CAIs) composed of Al-diopside, spinel, anorthite, and very rare melilite. Melilite is typically replaced by a fine-grained mixture of spinel, Al-diopside, and ±anorthite; spinel is replaced by anorthite. About 10% of AOAs contain low-Ca pyroxene replacing forsterite. Forsterite and spinel are always ¹⁶O-rich (δ^17,18O∼−40‰ to −50‰), whereas melilite, anorthite, and diopside could be either similarly ¹⁶O-rich or ¹⁶O-depleted to varying degrees; the latter is common in AOAs from altered and metamorphosed carbonaceous chondrites such as some CVs and COs. Low-Ca pyroxene is either ¹⁶O-rich (δ^17,18O∼−40‰) or ¹⁶O-poor (δ^17,18O∼0‰). Most AOAs in CV chondrites have unfractionated (∼2-10×CI) rare-earth element patterns. AOAs have similar textures, mineralogy and oxygen isotopic compositions to those of forsterite-rich accretionary rims surrounding different types of CAIs (compact and fluffy Type A, Type B, and fine-grained, spinel-rich) in CV and CR chondrites. AOAs in primitive carbonaceous chondrites show no evidence for alteration and thermal metamorphism. Secondary minerals in AOAs from CR, CM, and CO, and CV chondrites are similar to those in chondrules, CAIs, and matrices of their host meteorites and include phyllosilicates, magnetite, carbonates, nepheline, sodalite, grossular, wollastonite, hedenbergite, andradite, and ferrous olivine.Our observations and a thermodynamic analysis suggest that AOAs and forsterite-rich accretionary rims formed in ¹⁶O-rich gaseous reservoirs, probably in the CAI-forming region(s), as aggregates of solar nebular condensates originally composed of forsterite, Fe, Ni-metal, and CAIs. Some of the CAIs were melted prior to aggregation into AOAs and experienced formation of Wark-Lovering rims. Before and possibly after the aggregation, melilite and spinel in CAIs reacted with SiO and Mg of the solar nebula gas enriched in ¹⁶O to form Al-diopside and anorthite. Forsterite in some AOAs reacted with ¹⁶O-enriched SiO gas to form low-Ca pyroxene. Some other AOAs were either reheated in ¹⁶O-poor gaseous reservoirs or coated by ¹⁶O-depleted pyroxene-rich dust and melted to varying degrees, possibly during chondrule formation. The most extensively melted AOAs experienced oxygen isotope exchange with ¹⁶O-poor nebular gas and may have been transformed into magnesian (Type I) chondrules. Secondary mineralization and at least some of the oxygen isotope exchange in AOAs from altered and metamorphosed chondrites must have resulted from alteration in the presence of aqueous solutions after aggregation and lithification of the chondrite parent asteroids.  相似文献   

Timescales for the evolution of oxygen isotope compositions in the solar nebula     

J.R. Lyons  E.A. Bergin  A.M. Davis  K. Hashizume 《Geochimica et cosmochimica acta》2009,73(17):4998-6266

We review two models for the origin of the calcium-, aluminum-rich inclusion (CAI) oxygen isotope mixing line in the solar nebula: (1) CO self-shielding, and (2) chemical mass-independent fractionation (MIF). We consider the timescales associated with formation of an isotopically anomalous water reservoir derived from CO self-shielding, and also the vertical and radial transport timescales of gas and solids in the nebula. The timescales for chemical MIF are very rapid. CO self-shielding models predict that the Sun has Δ¹⁷O_SMOW ∼ −20‰ (Clayton, 2002), and chemical mass-independent fractionation models predict Δ¹⁷O_SMOW ∼0‰. Preliminary Genesis results have been reported by McKeegan et al. (McKeegan K. D., Coath C. D., Heber, V., Jarzebinski G., Kallio A. P., Kunihiro T., Mao P. H. and Burnett D. S. (2008b) The oxygen isotopic composition of captured solar wind: first results from the Genesis. EOS Trans. AGU 89(53), Fall Meet. Suppl., P42A-07 (abstr)) and yield a Δ¹⁷O_SMOW of ∼ −25‰, consistent with a CO self-shielding scenario. Assuming that subsequent Genesis analyses support the preliminary results, it then remains to determine the relative contributions of CO self-shielding from the X-point, the surface of the solar nebula and the parent molecular cloud.The relative formation ages of chondritic components can be related to several timescales in the self-shielding theories. Most importantly the age difference of ∼1-3 My between CAIs and chondrules is consistent with radial transport from the outer solar nebula (>10 AU) to the meteorite-forming region, which supports both the nebular surface and parent cloud self-shielding scenarios. An elevated radiation field intensity is predicted by the surface shielding model, and yields substantial CO photolysis (∼50%) on timescales of 0.1-1 My. An elevated radiation field is also consistent with the parent cloud model. The elevated radiation intensities may indicate solar nebula birth in a medium to large cluster, and may be consistent with the injection of ⁶⁰Fe from a nearby supernova and with the photoevaporative truncation of the solar nebula at KBO orbital distances (∼47 AU). CO self-shielding is operative at the X-point even when H₂ absorption is included, but it is not yet clear whether the self-shielding signature can be imparted to silicates. A simple analysis of diffusion times shows that oxygen isotope exchange between ¹⁶O-depleted nebular H₂O and chondrules during chondrule formation events is rapid (∼minutes), but is also expected to be rapid for most components of CAIs, with the exception of spinel. This is consistent with the observation that spinel grains are often the most ¹⁶O-rich component of CAIs, but is only broadly consistent with the greater degree of exchange in other CAI components. Preliminary disk model calculations of self-shielding by N₂ demonstrate that large δ¹⁵N enrichments (∼ +800‰) are possible in HCN formed by reaction of N atoms with organic radicals (e.g., CH₂), which may account for ¹⁵N-rich hotspots observed in lithic clasts in some carbonaceous chondrites and which lends support to the CO self-shielding model for oxygen isotopes.  相似文献   

Presolar Grains and Their Isotopic Anomalies in Meteorites     

林杨挺  王世杰 《中国地球化学学报》2001,20(1):1-11

Study on presolar grains including diamond,silicon carbide,graphite,silicon nitrite(Si3N4),coundum and spinel isolated from meteorites is summarized in this paper.Except for nanometer-sized diamond,the other grains are micrometers to submicrometers in size.The presolar grains survived mainly in the fine-grained matrix of primitive chondrites and were isolated by chemical treatments.Diamond contains Xe isotopes(Xe-HL),typically produced in p-and r-processes,probably formed in supernovae.Mainstream silicon carbides are enriched in ^29,30Si and ^13C,but depleted in ^15N.They also contain various s-process products,consistent with calculations of AGB stars.Other silicon carbides exhibit much larger isotopic anomalies and are classified as groups X,Y,Z and AB.Among them,group X of SiC is characterized by enrichment of ^28Si and daughter isotopes of various short-lived nuclides,suggesting an origin from supernovae.Graphite can be divided into four density fractions with distince isotopic compositions.They may form in AGB stars,novae and supernovae,respctively,Si3N4 is similar to X-SiC in isotopic composition.Corundum is classified as four groups based on theid oxygen isotopic compositions.AGB and red giang stare are possible sources for the oxide.More comprehensive study of presolar grains,especially discovery of the other types of oxides and silicates,isotopic analyses of individual submicrometer-sized grains and distribution of presolar grains among various chemical groups and petropaphic types of chondrites will provide new information on nucleosynthesis,stellar evolution and formation of the solar nebula.  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   

Use of stable carbon isotope compositions of pyrolytically derived methane as maturity indices for carbonaceous materials     

H.Moses Chung  William M. Sackett 《Geochimica et cosmochimica acta》1979,43(12):1979-1988

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