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1.
A non-colloidal fraction separated by physical means from an HFHCl-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 HFHCl-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   

2.
The abundance and isotopic composition of Hg was determined in bulk samples of both the Murchison (CM) and Allende (CV) carbonaceous chondrites using single- and multi-collector inductively coupled plasma mass spectrometry (ICP-MS). The bulk abundances of Hg are 294 ± 15 ng/g in Murchison and 30.0 ± 1.5 ng/g in Allende. These values are within the range of previous measurements of bulk Hg abundances by neutron activation analysis (NAA). Prior studies suggested that both meteorites contain isotopically anomalous Hg, with δ196/202Hg values for the anomalous, thermal-release components from bulk samples ranging from −260 ‰ to +440 ‰ in Murchison and from −620 ‰ to +540 ‰ in Allende Jovanovic and Reed 1976a, Jovanovic and Reed 1976b, Kumar and Goel 1992. Our multi-collector ICP-MS measurements suggest that the relative abundances of all seven stable Hg isotopes in both meteorites are identical to terrestrial values within 0.2 to 0.5 ‰.On-line thermal-release experiments were performed by coupling a programmable oven with the single-collector ICP-MS. Powdered aliquots of each meteorite were linearly heated from room temperature to 900°C over twenty-five minutes under an Ar atmosphere to measure the isotopic composition of Hg released from the meteorites as a function of temperature. In separate experiments, the release profiles of S and Se were determined simultaneously with Hg to constrain the Hg distribution within the meteorites and to evaluate the possibility of Se interferences in previous NAA studies. The Hg-release patterns differ between Allende and Murchison. The Hg-release profile for Allende contains two distinct peaks, at 225° and 343°C, whereas the profile for Murchison has only one peak, at 344°C. No isotopically anomalous Hg was detected in the thermal-release experiments at a precision level of 5 to 30 ‰, depending on the isotope ratio. In both meteorites the Hg peak at ∼340°C correlates with a peak in the S-release profile. This correlation suggests that Hg is associated with S-bearing phases and, thus, that HgS is a major Hg-bearing phase in both meteorites. The Hg peak at 225°C for Allende is similar to release patterns of physically adsorbed Hg on silicate and metal grains. Prior studies suggested that the isotopic anomalies reported from NAA resulted from interference between 203Hg and 75Se. However, the amount of Se released from both meteorites, relative to Hg, is insufficient to produce all of the observed anomalies.  相似文献   

3.
The absolute isotope abundance of Ti has been determined in Ca-Al-rich inclusions from the Allende and Leoville meteorites and in samples of whole meteorites. The absolute Ti isotope abundances differ by a significant mass dependent isotope fractionation transformation from the previously reported abundances, which were normalized for fractionation using 46Ti48Ti. Therefore, the absolute compositions define distinct nucleosynthetic components from those previously identified or reflect the existence of significant mass dependent isotope fractionation in nature. We provide a general formalism for determining the possible isotope compositions of the exotic Ti from the measured composition, for different values of isotope fractionation in nature and for different mixing ratios of the exotic and normal components. The absolute Ti and Ca isotopic compositions still support the correlation of 50Ti and 48Ca effects in the FUN inclusions and imply contributions from neutron-rich equilibrium or quasi-equilibrium nucleosynthesis. The present identification of endemic effects at 46Ti, for the absolute composition, implies a shortfall of an explosive-oxygen component or reflects significant isotope fractionation. Additional nucleosynthetic components are required by 47Ti and 49Ti effects. Components are also defined in which 48Ti is enhanced.Bulk samples of carbonaceous meteorites (C2 and C3 types) show distinct excesses at 50Ti but no nonlinear effects at the other Ti isotopes. Other chondrites, including Orgueil (Cl), show no nonlinear effects. Relative to terrestrial Ti, a small isotope fractionation is found for only an enstatite chondrite. The Ti absolute compositions in Ca-Al-rich inclusions show significant isotope fractionation effects corresponding to an enhancement in the heavier isotopes relative to the lighter isotopes as compared to Ti in a TiO2 standard and in chondrites. The absence of a correlation of Ti isotope fractionation effects with those for Ca and Mg is indicative of multiple processes of condensation, volatilization and recondensation; however, the mechanisms causing the isotope fractionation are not well understood.  相似文献   

4.
Silicate from two unusual iron-rich meteorites were analyzed by the I-Xe and 40Ar-39Ar techniques, Enon, an anomalous iron meteorite with chondritic silicate, shows no loss of radiogenic 40Ar at low temperature, and gives a plateau age of 4.59 ± 0.03 Ga. Although the Xe data fail to define an I-Xe correlation (possibly due to a very low iodine content), the inferred PuU ratio is more than 2σ above the chondritic value, and the Pu abundance derived from the concentration of Pu-fission Xe is 6 times greater than the abundance inferred for Cl meteorites. These findings for Enon, coupled with data for IAB iron meteorites, suggest that presence of chondritic silicate in an iron-rich meteorite is diagnostic of an old radiometric age with little subsequent thermal disturbance. The Eagle Station pallasite, the most 16O-rich meteorite known, gives a complex 40Ar-39Ar age pattern which suggests a recent (?0.85 Ga) severe thermal disturbance. The absence of excess 129Xe, and the low trapped Ar and Xe contents, are consistent with this interpretation. The similarity between 40Ar-39Ar data for Eagle Station and for the olivine-rich meteorite Chassigny lends credence to the previous suggestion of a connection between Chassigny and pallasites, in the sense that similar processes operating at similar times on different parent bodies may have been involved in the formation of olivine in both types of meteorites.  相似文献   

5.
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 (Ne20Ne22 ? 8.5) and the controversial CCFXe component, enriched in the heavy Xe isotopes (Xe136Xe132 ? 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 Xe136Xe132 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   

6.
We report measurements of the absolute isotope abundance of Ca in Ca-Al-rich inclusions from the Allende and Leoville meteorites. Improved high precision measurements are reported also for 46Ca. We find that nonlinear isotope effects in Ca are extremely rare in these inclusions. The absence of nonlinear effects in Ca, except for the effects in FUN inclusions, is in sharp contrast to the endemic effects in Ti. One fine-grained inclusion shows an excess of 46Ca of (7 ± 1)%., which is consistent with addition of only 46Ca or of an exotic (1) component with 46Ca1 ~ 48Ca1. FUN inclusion EK-1-4-1 shows a small 46Ca excess of (3.3 ± 1.0)%.; this confirms that the exotic Ca components in EK-1-4-1 were even more deficient in 46Ca relative to 48Ca than is the case for normal Ca. The Ca in the Ca-Al-rich inclusions shows mass dependent isotope fractionation effects (as deduced from the absolute 40Ca44Ca) which have a range from ?3.8 to +6.7%. per mass unit difference. This range is a factor of 20 wider than the range previously established for bulk meteorites and for terrestrial and lunar samples. Ca and Mg isotope fractionation effects in the Ca-Al-rich inclusions are common and attributed to kinetic isotope effects which imply the production of the inclusions by complex sequences of condensation, vaporization and recondensation. A correlation was found between Ca and Mg isotope fractionation effects and inclusion type. A possible correlation between isotope fractionation and rare earth element abundance patterns is discussed.  相似文献   

7.
Isotopically anomalous Te is a by-product of the nuclear processes in zones of supernovae that have been proposed as sources for isotopically anomalous Xe. The calculated composition of the anomalous Te is roughly consistent with the disputed measurements made by Balladet al. (1979) and Oliveret al. (1979) of samples of the Allende meteorite with the exception that the large 123Te overabundance reported by Oliveret al. (1979) is not predicted by the theory.  相似文献   

8.
Recent results on cosmic ray interactions in lunar samples and meteorites resulting in production of stable and radionuclides, particle tracks and thermoluminescence are reviewed. A critical examination of26A1 depth profiles in lunar rocks and soil cores, together with particle track data, enables us to determine the long term average fluxes of energetic solar protons (>10 MeV) which can be represented by (J s,R o)=(125, 125). The lunar rock data indicate that this flux has remained constant for 5×105 to 2×106 years. Production rates of stable and radionuclides produced by galactic cosmic rays is given as a function of size and depth of the meteoroid. Radionuclide (53Mn,28Al) depth profiles in meteorite cores, whose preatmospheric depths are deduced from track density profiles are used to develop a general procedure for calculating isotope production rates as a function of meteoroid size. Based on the track density and22Ne/21Ne production rates, a criterion is developed to identify meteorites with multiple exposure history.22Ne/21Ne ratio <1·06 is usually indicative of deep shielded exposure. An examination of the available data suggests that the frequency of meteorites with multiple exposure history is high, at least 15% for LL, 27% for L and 31% for H chondrites. The epi-thermal and the thermal neutron density profiles in different meteorites are deduced from60Co and track density data in Dhajala, Kirin and Allende chondrites. The data show that the production profile depends sensitively on the size and the chemical composition of the meteoroid. Cosmic ray-induced thermoluminescence in meteorites of known preatmospheric sizes has been measured which indicates that its production profile is nearly flat and insensitive to the size of the meteoroid. Some new possibilities in studying cosmic ray implanted radionuclides in meteorites and lunar samples using resonance ionisation spectroscopy are discussed.  相似文献   

9.
To simulate trapping of noble gases by meteorites, we reacted 15 FeCr or FeCrNi alloy samples with CO, H2O or H2S at 350–720 K, in the presence of noble gases. The reaction products, including (Fe,Cr)2O3, FeCr2S4, FeS, C, and Fe3C, were analyzed by mass spectrometry, usually after chemical separation by selective solvents. Three carbon samples were prepared by catalytic decomposition of CO or by dehydration of carbohydrates with H2SO4.The spinel and carbon samples were similar to those of earlier studies (Yang et al., 1982 and Yang and Anders, 1982), with only minor effects attributable to the presence of Ni. All samples sorted substantial amounts of noble gases, with distribution coefficients of 10?1–10?2 cm3 STP/g atm for Xe. On the basis of release temperature three gas components were distinguished: a generally dominant physisorbed component (20–80% of total), and two more strongly bound, chemisorbed and trapped components. Judging from the elemental pattern, the adsorbed components were acquired at the highest noble gas partial pressure encountered by the sample—atmosphere or synthesis vessel.Sulfides, particularly daubréelite, showed three distinctive trends relative to chromite or magnetite: the high-T component was larger, 30–70% of the total; NeXe ratios were higher, by up to 102, possibly due to preferential diffusion of Ne during synthesis. In one synthesis, at relatively high P, the gases were sorbed with only minimal elemental fractionation, presumably by occlusion.Most of the features of primordial noble gases can be explained in terms of the data and concepts presented in the three papers of this series. The elemental fractionation pattern of Ar, Kr, Xe in meteorites, terrestrial rocks, and planets resembles the adsorption pattern on the solids studied: carbon, spinels, Sulfides, etc. The variation in NeAr ratio may be explained by preferential diffusion of Ne. The high release temperature of meteoritic noble gases may be explained by transformation of physisorbed to chemisorbed gas, as observed in some experiments. The ready loss of meteoritic heavy gases on surficial oxidation (“Phase Q”) is consistent with adsorption, as is the high abundance. Extrapolation of the limited laboratory data suggests that the observed amounts of noble gases could have been adsorbed from a solar gas at 160–170 K and 10?6–10?5 atm, i.e. in the early contraction stages of the solar nebula. The principal unsolved problem is the origin of isotopically anomalous, apparently mass-fractionated noble gases in the Earth's atmosphere and in meteoritic carbon and chromite.  相似文献   

10.
We describe the analytical techniques developed for the precise measurement of the titanium isotope abundances using a TiO+ ion beam. Terrestrial, lunar, and bulk meteorite samples yield identical results. Using a normalization to 46Ti48Ti for mass dependent isotope fractionation, we obtain the normal Ti composition: 46Ti48Ti = 0.108548; 47Ti48Ti = 0.099315 ± 0.000005; 49Ti48Ti = 0.074463 ± 0.000004; 50Ti48Ti = 0.072418 ± 0.000004 (2σ grand mean), taking 18O16O = 0.002045 and 17O16O = 0.00037. Measurements on thirteen coarse-grained and fine-grained Ca-Al-Ti-rich inclusions from the Allende and Leoville meteorites show the presence of widespread, significant, nonlinear isotope anomalies in the Ti isotopes which were not used for normalization. The data require the addition of at least three exotic components. The distinct correlation of non-linear effects for the most neutron-rich isotopes of Ca and Ti and the absence of substantial effects at 46Ca in the FUN samples EK-1-4-1 and C-1 indicate that the effects reflect neutron-rich equilibrium or quasi-equilibrium nucleosynthetic processes in the outer layers of a supernova core. The results on Ca and Ti in conjunction with the isotopic effects on other elements (Mg, Sr, Ba, Nd, Sm) show that the samples represent mixtures of different nucleosynthetic components from distinctive processes (‘e’, ‘r’, ‘p’) which do not appear to be related to processes in the same stellar sites.  相似文献   

11.
We measured the 153Eu/151Eu ratio by MC-ICP-MS for a terrestrial basalt, two terrestrial soils, and four meteorites (whole rocks and/or chondrules of Bjurböle, Forest City, Murchison, and Allende) and found no isotopic variations. By contrast, two CAI separates from two different pieces of Allende show a 153Eu deficit of up to one per mil. Such a shortage in the heavy isotopes, which had also been identified in Allende CAIs for Sr [Patchett, P.J. 1980b. Sr isotopic fractionation in Allende chondrules: a reflection of solar nebular processes. Earth Planet. Sci. Lett.50, 181-188], cannot reflect evaporative fractionation. The lack of Sm isotope fractionation in the same samples further makes fractionation by purely kinetic processes an unlikely cause of the anomalous Eu isotopic composition. An alternative interpretation is condensation from a vapor already significantly depleted in Eu, but in such a scenario the fate of the missing material is unclear. We therefore prefer yet another interpretation, based on the low ionization potential of Eu (and Sr), in which electromagnetic separation of the ionized gas preferentially depletes the nebular gas in heavy isotopes.  相似文献   

12.
Samples studied were residual, carbonaceous /Alates—a coined word to designate colloids prepared sometimes before and sometimes after acid demineralization—from Murray, Murchison, Cold Bokkeveld (type C2s) and Allende (type CV3) meteorites. Characterization: C2 /Alates, comprising 0.5% of the bulk meteorite are fine-grained (< 100 Å), amorphous, sulfide-free, oxidizable, 95% carbonaceous materials which pyrolyze bimodally at 200–700 and 800–1200°C. Allende /Alates are similar but with traces of inferred spinel and chromite and of sulfur, Rare gas results: Elemental: Release from stepwise heated Murray is bimodal with maximum release and upper temperature peak at 1000°C, probably accompanying chemical reaction. All /Alates studied had very nearly the same elemental concentrations, distinctly planetary in pattern. Isotopic: Trapped neon compositions are unprecedentedly close to Pepin's neon-A corner but nevertheless show signs of complexity, as if accompanied by neon-E. The trapped 3He/4He ratio is essentially constant at (1.42 ± 0.2 × 10?4. The isotopically anomalous heavy noble gases, easily detected in the residues of oxidized /Alates, were not conspicuous in this particular study. Comparison and Chicago results: Concentrations of heavy rare gases in our /Alates agree with concentrations measured directly (as opposed to inferred by difference) in acid resistant residues at Chicago. Alone, our results support the idea of a carbonaceous gas-carrier uniformly present in meteorites of various types, but Chicago characterizations of the samples can apply to both their samples and ours provided that the right amount of gas was lost in the Berkeley procedures to make the uniform gas contents in various samples a coincidence.  相似文献   

13.
High-precision analyses of Ti are reported for samples from a variety of meteorite classes. The expanded data base for Allende inclusions still shows Ti isotopic anomalies in every inclusion. All the coarse-grained inclusions give quite similar patterns, but fine-grained inclusions show more variable, and sometimes larger, anomalies. One inclusion, 3675A, was analyzed because others identified it as a possible “FUN” inclusion due to its mass-fractionated Mg. This designation is supported by the significantly more complex Ti isotopic pattern for 3675A compared to all our other Allende inclusions. Available data fail to suggest that any particular Allende mineral phase, including a chromite-carbon fraction from an acid residue, is especially rich in anomalous Ti. We also find anomalous Ti in a bulk sample of a Cl chondrite and in matrix separates from C2 chondrites. The excesses of 50Ti are smaller than for Allende inclusions, and subtle differences in Ti isotopic patterns tentatively suggest that parent materials for C1-C2 matrix and Allende inclusions are not directly related. Analyses of chondrules from unequilibrated ordinary chondrites did not yield clear evidence for anomalous Ti, but some “larger than usual” deficits at 5046 give encouragement for future work in this direction. Comparing the magnitude of isotopic shifts at 50Ti and 16O for all these meteorite samples indicates that they are not correlated, but the data do not preclude a correlation between concentrations of “exotic” 50Ti and 16O atoms.Whether or not Allende “FUN” inclusions are considered, at least 4 distinct isotopic components of Ti are required to account for the observed isotopic variations. The Ti data cannot be plausibly explained in terms of an early solar-system particle irradiation; instead, neutron-rich hydrostatic burning within a star is probably responsible for the dominant 50Ti anomalies, while s-process mechanisms are viable sources for some of the more subtle Ti variations. We suggest that the Ti anomalies are linked to a diversity of nucleosynthetic sources and the highly refractory behavior of Ti. Therefore, some form of “chemical memory” from the ISM, rather than “late stage supernova injection”, is most likely responsible for the preservation of observed isotopic heterogeneities.  相似文献   

14.
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’ PdNi 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   

15.
The sulphur isotope composition of 233 sulphides and 40 sulphates has been investigated and evaluated in combination with 29 earlier published data. The total variation of δ34S values for the sulphides and the sulphates ranges from ?40 up to ?1 ‰ and from +7 up to +20 ‰, respectively. For the mineral species the variations are (with number of samples in brackets): galena (96) ?32 up to ?2 ‰, sphalerite (141) ?30 up to ?4 ‰, marcasite (16) ?27 up to ?1 ‰, pyrite (10) ?26 up to ?13 ‰, molybedenite (3) ?40 up to ?29 ‰, anhydrite and gypsum (8) +15 up to +20 ‰, coelestine (1) +19 ‰, and barite (33) +7 up to +18 ‰. The frequency distribution of the δ34S values corresponds with the complexity of the ore forming processes which resulted in six strata-bound ore mineralizations. The sulphate values clearly show that the sulphate sulphur originates from sea water sulphate. The sulphides are formed by bacteriogeneric processes from seawater sulphate, and their sulphur isotope composition depends on the lithofacies of the sediments as well as on the following diagenetic processes.  相似文献   

16.
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 (Fo50–65). Olivine in rimmed olivine aggregates (Type 1B inclusions) is, on average, more magnesian, with a wider compositional range (Fo53–96). 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 FeMg equilibration (without textural homogenization) in the meteorite parent body.  相似文献   

17.
Uranium distributions have been determined in seventeen meteorites using fission track techniques. In seven cases, Th was also determined by a new method using fast neutrons. The actinides are generally concentrated in phosphates, usually whitlockite and/or chlorapatite. Wherever whitlockite and chlorapatite coexist, chlorapatite is richer in uranium. U concentrations in a given phosphate phase are highly variable from meteorite to meteorite and sometimes also show large variations in the same meteorite. A clinopyroxene phase enriched in U (0.2–0.3 ppm) is usually found in Ca-rich achondrites. The ThU ratios of phosphates differ considerably from whole rock values indicating that these elements were fractionated during the meteorite formation.  相似文献   

18.
A new condensation sequence appears if the CO ratio in a gas of otherwise solar composition is increased by less than a factor of two. As the ratio increases from the solar value of 0.6 to ? 1 the gas becomes extremely reduced, the condensation temperatures of silicates and oxides are depressed markedly ~ 400 K and a new suite of refractory minerals appears: AIN, CaS, MgS, SiC, TiN, graphite, Si2N2O and probably metastable (Fe,Ni)3C. Many of these minerals are unique to enstatite chondrites and may be analogues of the refractory silicates and oxides found in more oxidized meteorites such as Allende.The change in chemistry is related to the stability of CO, the most stable C or O compound at high T. Since the elements occur in a 1:1 ratio in CO, only the element which is in excess is free to form other compounds. But as T decreases CO reacts with H2 to form graphite, CH4 or other hydrocarbons thereby freeing O to form H2O. If equilibrium is maintained oxides and silicates form at about 1000 K (CO > 1, Pτ = 10?4atm) as products of reactions among the carbides, nitrides, sulfides and the gas. The possibility that equilibrium was not maintained among the C-bearing species was also investigated. If either graphite or CH4 does not form as predicted the stability fields of the reduced minerals expands to lower temperatures. If neither graphite nor CH4 form as predicted, CO remains stable and the nebular gas is highly reduced at all temperatures.Enstatite chondrites appear to have originated in a region of the nebula where the CO ratio was somewhat higher than the solar value. Various fractionation mechanisms are considered. An interesting possibility is that graphite, which is quite refractory under a wide range of conditions, survived the collapse of the solar nebula.  相似文献   

19.
Al26 and noble gas contents of 6 ordinary chondrites with He3Ne21 ratios above 6.0 or below 4.0 are used to infer the variability of the production rates of He3 and Ne21 (PHe3 and PNe21). The ratio of the observed Al26 content to a calculated, normal value is taken as a measure of the change of PNe21 from its normal value. The corresponding change in PHe3 is then computed from the observed He3Ne21 ratio and an average value of PHe3.According to these calculations which exclude orbital effects, PHe3 will be near the average value in meteorites with high He3Ne21 ratios, while PNe21 will be about 30 per cent below normal. In meteorites with low He3Ne21 ratios, PHe3 may be depressed by as much as 25 per cent from normal while PNe21 may be 15–20 per cent above the average.  相似文献   

20.
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 DH 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 DH ratios are greater than 30 × 10?5. If the DH 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 DH 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 DH ratios in organic compounds in interstellar clouds are typically 180 × 10?5 and range between about 40 × 10?5 and 5000 × 10?5. The DH 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 DH ratios.In contrast, the DH 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 13C12C ratios of organic matter, irrespective its DH ratio, lie well within those observed for the earth. If organic matter originated in the interstellar medium, our data would indicate that the 13C12C 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 DH 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   

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