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1.
In the present work an attempt has been made to investigate statistical association between solar neutrino flux data (both D2O and Salt data) collected from Sudbury Neutrino Observatory and solar irradiance data detected by Earth Radiation Budget Satellite. To serve the present purpose we have used the Multifractal Detrended Cross Correlation Analysis (MF-DCCA) based on Detrended Fluctuation Analysis (MF-X-DFA) method and the Detrending Moving Average Analysis (MF-X-DMA) which explores the long term power-law cross correlations between above two pairs of data sets. Investigation also has been made to find the frequency and time dependent local phase relationship in each pair of data sets using continuous wavelet transform (CWT) based Semblance Analysis. The Semblance Analysis reveals that there exists positive phase correlation as well as negative phase correlation between solar irradiance and D2O data at different time sub-intervals. This type of mixed phase correlation is also experienced between solar irradiance and Salt data at different time sub-intervals. The causal relationship between the D2O and the solar irradiance time series and that between Salt and solar irradiance time series have been revealed using Singular Spectral Analysis (SSA). Calculations indicate that possibly the present solar neutrino flux data (both D2O and Salt data) is supportive to predict the solar irradiance data but may not the vice versa which in turn suggests that the variability of nuclear energy generation process inside the Sun may influence the solar activity.  相似文献   

2.
Abstract— Grain-by-grain analytical electron microscope analyses of two micrometeorites, or interplanetary dust particles (IDPs), of the chondritic porous subtype, show the presence of rare barite (BaSO4) and magnesium carbonate, probably magnesite. Salt minerals in chondritic porous (CP) IDPs give evidence for in situ aqueous alteration in their parent bodies. The uniquely high barium content of CP IDP W7029*C1 is consistent with barite precipitation from a mildly acidic (pH > ～5) aqueous fluid at temperatures below 417 K and low oxygen fugacity. The presence of magnesite in olivine-rich, anhydrous CP IDP W7010*A2 is evidence that carbonate minerals occur in both the chondritic porous and chondritic smooth subtypes of chondritic IDPs. Citing Schramm et al. (1989) for putative asteroidal-type aqueous alteration in IDPs and probable sources of chondritic IDPs, salt minerals in CP IDPs could support low-temperature aqueous activity in nuclei of active short-period comets.  相似文献   

3.
Abstract– Fragments of magnesian anorthositic granulite are found in the lunar highlands meteorites Allan Hills (ALH) A81005 and Dhofar (Dho) 309. Five analyzed clasts of meteoritic magnesian anorthositic granulite have Mg′ [molar Mg/(Mg + Fe)] = 81–87; FeO ≈ 5% wt; Al2O3 ≈ 22% wt; rare earth elements abundances ≈ 0.5–2 × CI (except Eu ≈ 10 × CI); and low Ni and Co in a non‐chondritic ratio. The clasts have nearly identical chemical compositions, even though their host meteorites formed at different places on the Moon. These magnesian anorthositic granulites are distinct from other highlands materials in their unique combination of mineral proportions, Mg′, REE abundances and patterns, Ti/Sm ratio, and Sc/Sm ratio. Their Mg′ is too high for a close relationship to ferroan anorthosites, or to have formed as flotation cumulates from the lunar magma ocean. Compositions of these magnesian anorthositic granulites cannot be modeled as mixtures of, or fractionates from, known lunar rocks. However, compositions of lunar highlands meteorites can be represented as mixtures of magnesian anorthositic granulite, ferroan anorthosite, mare basalt, and KREEP. Meteoritic magnesian anorthositic granulite is a good candidate for the magnesian highlands component inferred from Apollo highland impactites: magnesian, feldspathic, and REE‐poor. Bulk compositions of meteorite magnesian anorthositic granulites are comparable to those inferred for parts of the lunar farside (the Feldspathic Highlands Terrane): ～4.5 wt% FeO; ～28 wt% Al2O3; and Th <1 ppm. Thus, magnesian anorthositic granulite may be a widespread and abundant component of the lunar highlands.  相似文献   

4.
Abstract— We present the results of irradiation experiments aimed at understanding the structural and chemical evolution of silicate grains in the interstellar medium. A series of He+ irradiation experiments have been performed on ultra‐thin olivine, (Mg,Fe)2SiO4, samples having a high surface/volume (S/V) ratio, comparable to the expected S/V ratio of interstellar dust. The energies and fluences of the helium ions used in this study have been chosen to simulate the irradiation of interstellar dust grains in supernovae shock waves. The samples were mainly studied using analytical transmission electron microscopy. Our results show that olivine is amorphized by low‐energy ion irradiation. Changes in composition are also observed. In particular, irradiation leads to a decrease of the atomic ratios O/Si and Mg/Si as determined by x‐ray photoelectron spectroscopy and by x‐ray energy dispersive spectroscopy. This chemical evolution is due to the differential sputtering of atoms near the surfaces. We also observe a reduction process resulting in the formation of metallic iron. The use of very thin samples emphasizes the role of surface/volume ratio and thus the importance of the particle size in the irradiation‐induced effects. These results allow us to account qualitatively for the observed properties of interstellar grains in different environments, that is, at different stages of their evolution: chemical and structural evolution in the interstellar medium, from olivine to pyroxene‐type and from crystalline to amorphous silicates, porosity of cometary grains as well as the formation of metallic inclusions in silicates.  相似文献   

5.
Al–Mg mineral isochron studies using secondary ion mass spectrometry (SIMS) have revealed the initial 26Al/27Al ratios, (26Al/27Al)0, for individual Ca-Al-rich inclusions (CAIs) in meteorites. We find that the relative sensitivity factors of 27Al/24Mg ratio for SIMS analysis of hibonite, one of the major constituent minerals of CAIs, exhibit variations based on their chemical compositions. This underscores the critical need for using appropriate hibonite standards to obtain accurate Al−Mg data. We measured the Al−Mg mineral isochron for hibonite in a fine-grained CAI (FGI) from the Northwest Africa 8613 reduced CV chondrite by SIMS using synthesized hibonite standards with 27Al/24Mg of ~30, ~100, and ~400. The obtained mineral isochron of hibonite in the FGI yields (26Al/27Al)0 of (4.73 ± 0.09) × 10−5, which is identical to that previously obtained from the mineral isochron of spinel and melilite in the same FGI (Kawasaki et al., 2020). The uncertainties of (26Al/27Al)0 indicate that the constituent minerals in the FGI formed within ~0.02 Myr in the earliest solar system. The disequilibrium O-isotope distributions of the minerals in the FGI suggest that the O-isotope compositions of the nebular gas from which they condensed underwent a transitional change from 16O-rich to 16O-poor within ~0.02 Myr in the earliest solar system. Once formed, the FGI may have been removed from the forming region within ~0.02 Myr and transported to the accretion region of the parent body.  相似文献   

6.
Simon Petrie 《Icarus》2004,171(1):199-209
We report results of quantum chemical calculations of Mg+/ligand bond dissociation energies involving ligands identified as major constituents of Titan's upper atmosphere. Trends identified in these results allow elucidation of the important bimolecular and termolecular reactions of Mg+, and of simple molecular ions containing Mg+, arising from meteoric infall into Titan's atmosphere. Our study highlights, and includes calculated rate coefficients for, crucial ligand-switching and ligand-stripping reactions which ensure that a dynamic equilibrium exists between atomic and molecular ions of Mg+. Neutralization of ionized meteoric Mg is expected to produce the radical MgNC in high yield. The highly polar MgNC radical should provide an excellent nucleation site for condensation of polar (e.g., HCN, CH3CN, and HC3N) and highly unsaturated (e.g., C2H2, C4H2, and C2N2) neutrals at comparatively high altitude, leading to precipitation of Mg-doped tholin-like material. The implications for Titan's prebiotic chemical evolution, of the surface deposition of such material (which may feasibly contain magnesium porphyrins, or other bioactive Mg-containing complexes) remain to be assessed.  相似文献   

7.
Abstract— The Carcote meteorite, detected in 1888 in the northern Chilean Andes, is a brecciated, weakly shocked H5 chondrite. It contains a few barred olivine chondrules and, even more rarely, fan-shaped or granular orthopyroxene chondrules. The chondrules are situated in a fine-grained matrix that consists predominantly of olivine and orthopyroxene with accessory clinopyroxene, troilite, chromite, merrillite, and plagioclase. The metal phase is mainly kamacite with subordinate taenite and traces of native Cu. In its bulk rock composition, Carcote compares well with other H5 chondrites so far analysed, except for a distinctly higher C content. Microprobe analyses revealed the following mineral compositions: olivine (Fa16.5–20), orthopyroxene (Fs14–17.5), diopsidic clinopyroxene (FS6–7), plagioclase (An15–20). Troilite is stoichimetric FeS with traces of Ni and Cr; chromite has Cr/(Cr + Al) of 0.86, Fe2+/(Fe2+ + Mg) of 0.80-0.88 and contains considerable amounts of Ti, Mn, and Zn. Merrillite is close to the theoretical formula Ca18(Mg, Fe)2Na2(PO4)14, although with a Na deficiency not compensated for by excess Ca; the Mg/(Mg + Fe2+) ratio of the Carcote merrilite is 0.93-0.95. Kamacite and taenite have Ni contents of 5.6–7.2 and 17.1–23.4 wt%, respectively. Native Cu contains about 3.1–3.3 wt% Fe and 1.6 wt% Ni. Application of different geothermometers to the Carcote H5 chondrite yielded apparently inconsistent results. The highest temperature range of 850–950 °C (at 1 bar) is derived from the Ca-in-opx thermometer. From the cpx-opx solvus geothermometers and the two-pyroxene Fe-Mg exchange geothermometer, a lower temperature range of 750–840 °C is estimated, whereas lower and more variable temperatures of 630–770 °C are obtained from the Ca-in-olivine geothermometer. Recent calibrations of the olivine-spinel geothermometer yielded a still lower temperature range of 570–670 °C, which fits well to the temperature information derived from the Ni distribution between kamacite and taenite. Judging from crystal chemical considerations, we assume that these different temperatures reflect the closure of different exchange equilibria during cooling of the meteorite parent body.  相似文献   

8.
Abstract– Mg isotope data were collected by NanoSIMS with high‐precision and high‐spatial resolution from a coarse‐grained type B Ca‐, Al‐rich inclusion (CAI), EK1‐6‐3, in the Allende CV3 chondrite to evaluate the time scale of parent body thermal metamorphism. The CAI melilite and fassaite contain excesses of 26Mg (26Mg*) from the in‐situ decay of 26Al; the inferred initial ratio, (26Al/27Al)0 = (5.8 ± 2.4) × 10?5, is consistent with many previously reported coarse‐grained CAIs from CV chondrites (e.g., MacPherson et al. 1995 ). However, the anorthite has heterogeneous (26Al/27Al)0, ranging from 1.8 × 10?5 to 3.3 × 10?6. The 26Al‐26Mg systematics within the anorthite is consistent with thermal diffusion of Mg isotopes during metamorphism. We also show that the heterogeneous distribution of 26Mg* in anorthite could have resulted from thermal diffusion of 26Mg* over a 0.6–0.8 Ma time span. Mg diffusion thus may be responsible for the (26Al/27Al)0 heterogeneity within anorthite in CAIs.  相似文献   

9.
Within Gusev Crater and Meridiani Planum on Mars, the Mars exploration rovers have found Br concentrations in soils and rocks in the hundreds of ppm range. Relative to Earth compositions, these are high Br concentrations. Because of low Br concentrations on Earth, Br largely precipitates from seawater as a minor constituent in halite crystals rather than as a separate phase mineral. This is also likely to be the case for Mars. But given that the surface chemistries on Mars are significantly different than on Earth, minerals other than halite could serve as sinks for Br. The specific objectives of this paper were to (1) incorporate Br solution phase chemistries into the FREZCHEM model, (2) integrate the Siemann–Schramm Br/Cl mineral model into FREZCHEM, and (3) apply this mineral model to Br/Cl partitioning in Burns formation rocks as an indicator of past environments in the Meridiani Planum region of Mars. We showed that: (1) a molar-based model for Br substitution into halite and bischofite provided a better fit to experimental data than the standard mass-based model; (2) the concentrations of all of the soluble salts (mainly of Na, Mg, Ca, Cl, Br, and SO4) in the Burns formation, except for Ca, were significantly related to stratigraphic depth; (3) the likely precipitation of Ca as gypsum on Mars precluded Ca precipitating as a CaCl2 salt and thus impacts the possible minimum eutectic brine temperatures relevant to the Burns formation; (4) bischofite (MgCl2⋅6H2O) was a much more important sink for Br than halite; (5) Br/Cl patterns in the Burns formation, and within the three formation layers, argued in support of salt upwelling through groundwater evaporation; and (6) the high concentrations of Br in the surface layers of the Burns formation suggested that there was little water leaching and removal of soluble phases from the upper part of the stratigraphic succession.  相似文献   

10.
Evaporation of solid materials under low-pressure conditions could play important roles in chemical and isotopic fractionations in the early solar system. We have studied anisotropy of isotopic fractionation of 26Mg and 25Mg during kinetic evaporation of forsterite (Mg2SiO4), which is potentially a powerful tool to understand thermal histories of crystals in the early solar system. Ion-microprobe depth profiling revealed that the Mg isotopic zoning profiles of forsterite evaporated at 1500-1700 °C are notably differing along the a-, b-, and c-axes, which can be attributed to anisotropy in self-diffusion coefficient of Mg (D) and an isotopic fractionation factor for evaporation of Mg (α). The D and α were obtained from zoning profiles by applying the diffusion-controlled isotopic fractionation model of Wang et al. [1999. Evaporation of single crystal forsterite: Evaporation kinetics, magnesium isotope fractionation, and implications of mass-dependent isotopic fractionation of a diffusion-controlled reservoir. Geochim. Cosmochim. Acta 63(6), 953-966.].The D is largest and smallest along the a- and c-axes, respectively. The activation energy of 560-670 kJ/mol indicates that Mg diffusion at 1500-1700 °C occurred in the intrinsic diffusion regime.The α seems to be larger along the a- or c-axes than along the b-axis. The α along the a- or c-axes show weak temperature dependence. The α along all the crystallographic orientations is closer to unity than that expected from the kinetic theory of gases. These lines of evidence suggest that surface processes such as breaking of bonds and surface diffusion are responsible for the isotopic fractionation.  相似文献   

11.
NASA’s Phoenix lander identified perchlorate and carbonate salts on Mars. Perchlorates are rare on Earth, and carbonates have largely been ignored on Mars following the discovery by NASA’s Mars Exploration Rovers of acidic precipitated minerals such as jarosite. In light of the Phoenix results, we updated the aqueous thermodynamic model FREZCHEM to include perchlorate chemistry. FREZCHEM models the Na-K-Mg-Ca-Fe(II)-Fe(III)-Al-H-Cl-Br-SO4-NO3-OH-HCO3-CO3-CO2-O2-CH4-Si-H2O system, with 95 solid phases. We added six perchlorate salts: NaClO4·H2O, NaClO4·2H2O, KClO4, Mg(ClO4)2·6H2O, Mg(ClO4)2·8H2O, and Ca(ClO4)2·6H2O. Modeled eutectic temperatures for Na, Mg, and Ca perchlorates ranged from 199 K (−74 °C) to 239 K (−34 °C) in agreement with experimental data.We applied FREZCHEM to the average solution chemistry measured by the Wet Chemistry Laboratory (WCL) experiment at the Phoenix site when soil was added to water. FREZCHEM was used to estimate and alkalinity concentrations that were missing from the WCL data. The amount of is low compared to estimates from elemental abundance made by other studies on Mars. In the charge-balanced solution, the dominant cations were Mg2+ and Na+ and the dominant anions were , and alkalinity. The abundance of calcite measured at the Phoenix site has been used to infer that the soil may have been subject to liquid water in the past, albeit not necessarily locally; so we used FREZCHEM to evaporate (at 280.65 K) and freeze (from 280.65 to 213.15 K) the WCL-measured solution to provide insight into salts that may have been in the soil. Salts that precipitated under both evaporation and freezing were calcite, hydromagnesite, gypsum, KClO4, and Mg(ClO4)2·8H2O. Epsomite (MgSO4·7H2O) and NaClO4·H2O were favored by evaporation at temperatures >0 °C, while meridianite (MgSO4·11H2O), MgCl2·12H2O, and NaClO4·2H2O were favored at subzero temperatures. Incongruent melting of such highly hydrated salts could be responsible for vug formation elsewhere on Mars.All K+ precipitated as insoluble KClO4 during both evaporation and freezing simulations, accounting for 15.8% of the total perchlorates. During evaporation, 35.8% of perchlorates precipitated with Na+ and 48.4% with Mg2+. During freezing, 58.4% precipitated with Na+ and 24.8% with Mg2+. Given its low eutectic temperature, the existence of Mg(ClO4)2 in either case allows for the possibility of liquid brines on Mars today. FREZCHEM also showed that Ca(ClO4)2 would likely not have precipitated at the Phoenix landing site due to the strong competing sinks for Ca as calcite and gypsum. Overall, these results help constrain the salt mineralogy of the soil. Differences between evaporites and cryogenites suggest ways to discriminate between evaporation and freezing during salt formation. Future efforts, such as sample return or in situ X-ray diffraction, may make such a determination possible.  相似文献   

12.
Frans J.M. Rietmeijer 《Icarus》2011,211(2):948-959
Chondrite aggregate interplanetary dust particle IDP L2011K7, collected in the Earth’s lower stratosphere, is an agglomerate of diopside, Mg,Fe-olivine, rare Fe-sulfide and abundant amorphous Mg,Fe-silicates. The overwhelming majority of amorphous silicates have a serpentine-dehydroxylate [(Mg,Fe)3Si2O7] composition; a few have a smectite-dehydroxylate [(Mg,Fe)6Si8O22] composition. The cation ratios of the amorphous silicates are notably identical to those of serpentine and smectite phyllosilicates. This paper follows the chronological changes in the amorphous silicates that include (1) formation of nanometer scale crystalline silicates (Mg,Fe-olivine and pyroxene), (2) partial hydration and formation of antigorite-serpentine proto-phyllosilicates, (3) partial dehydration of these proto-phyllosilicates, and finally oxidation and Fe-oxide formation by flash heating during atmospheric entry. Environmental conditions capable of driving these changes in the diffuse interstellar medium or solar nebula, in a comet nucleus, or in circumsolar orbit as a cometary meteoroid were marginal at best. These changes could only proceed because of the unique amorphous silicate compositions. While this study cannot make a firm statement about an interstellar or solar nebula origin for its amorphous silicates that are irradiation-induced olivine, this study does find that amorphous silicates with serpentine and (rare) smectite compositions are an important fraction of the amorphous silicates in comets in addition to amorphous olivine and pyroxene. It is noted that an ice and water-free, millimeter-scale, structurally coherent crumb would be an ample ‘microenvironment’ to evolve micrometer-scale dust. After all IDP L2011K7 only measures 22 × 17 μm.  相似文献   

13.
Merrillite is a ubiquitous accessory phase in a variety of Martian meteorite lithologies. The Martian merrillites exhibit a positive correlation between Mg# and Na and a negative correlation between Mg# and both Mn and vacancies in the octahedral Na‐site. Their REE patterns are varied and range from LREE‐depleted to LREE‐enriched. The dominant cation substitutions in the Martian merrillites are Fe2+VI Mg‐site?Mg2+VI Mg‐site and Ca2+VI Na‐site +  □VI Na‐site?2Na+VI Na‐site. The REE substitution into the 8‐fold coordinated Ca‐site is accommodated by the coupled substitution CaVIII Ca‐site + (Na)VI Na‐site ?(Y3+ + REE3+)VIII Ca‐site + □VI Na‐site. The REE substitution is significantly more prevalent in lunar merrillite and can be used as a “fingerprint” to distinguish lunar from Martian meteorites. The substitution of OH? (whitlockite) and/or F? (bobdownsite) for O2? on one of the phosphate tetrahedrons appears to be rather insignificant. The correlations among Na, Mg#, Mn, and Na‐site vacancies are linked to the premerrillite crystallization history of the melt and the crystal chemical behavior of the Mg‐ and Na‐sites. The former reflects the sequence and extent of plagioclase and pyroxene crystallization. The differences in REE pattern shapes among the merrillites reflect source regions for the Martian basalts and the shapes are not greatly perturbed by the crystallization history. The occurrence of merrillite does not imply low‐volatile component in the Martian magmas. However, the low whitlockite and bobdownsite contents suggest that these samples were not altered by hydrothermal fluids and therefore not reset owing to aqueous fluid interactions. Consequently, the young ages of the shergottites are probably true igneous crystallization ages.  相似文献   

14.
We studied 149 pyroxenes from 69 pyroxene-bearing micrometeorites collected from deep-sea sediments of the Indian Ocean and South Pole Water Well at Antarctica, Amundsen-Scott South Pole station. The minor elements in pyroxenes from micrometeorites are present in the ranges as follows: MnO ~0.0–0.4 wt%, Al2O3 ~0.0–1.5 wt%, CaO ~0.0–1.0 wt%, Cr2O3 ~0.3–0.9 wt%, and FeO ~0.5–4 wt%. Their chemical compositions suggest that pyroxene-bearing micrometeorites are mostly related to precursors from carbonaceous chondrites rather than ordinary chondrites. The Fe/(Fe+Mg) ratio of the pyroxenes and olivines in micrometeorites shows similarities to carbonaceous chondrites with values lying between 0 and 0.2, and those with values beyond this range are dominated by ordinary chondrites. Atmospheric entry of the pyroxene-bearing micrometeorites is expected to have a relatively low entry velocity of <16 km s−1 and high zenith angle (70–90°) to preserve their chemical compositions. In addition, similarities in the pyroxene and olivine mineralogical compositions between carbonaceous chondrites and cometary particles suggest that dust in the solar system is populated by materials from different sources that are chemically similar to each other. Our results on pyroxene chemical compositions reveal significant differences with those from ordinary chondrites. The narrow range in olivine and pyroxene chemical compositions are similar to those from carbonaceous chondrites, and a small proportion to ordinary chondrites indicates that dust is largely sourced from carbonaceous chondrite-type bodies.  相似文献   

15.
Mg‐phyllosilicate‐bearing, dark surface materials on the dwarf planet Ceres have NH4‐bearing materials, indicated by a distinctive 3.06 μm absorption feature. To constrain the identity of the Ceres NH4‐carrier phase(s), we ammoniated ground particulates of candidate materials to compare their spectral properties to infrared data acquired by Dawn's Visible and Infrared (VIR) imaging spectrometer. We treated Mg‐, Fe‐, and Al‐smectite clay minerals; Mg‐serpentines; Mg‐chlorite; and a suite of carbonaceous meteorites with NH4‐acetate to exchange ammonium. Serpentines and chlorites showed no evidence for ammoniation, as expected due to their lack of exchangeable interlayer sites. Most smectites showed evidence for ammoniation by incorporation of NH4+ into their interlayers, resulting in the appearance of absorptions from 3.02 to 3.08 μm. Meteorite samples tested had weak absorptions between 3.0 and 3.1 μm but showed little clear evidence for enhancement upon ammoniation, likely due to the high proportion of serpentine and other minerals relative to expandable smectite phases or to NH4+ complexing with organics or other constituents. The wavelength position of the smectite NH4 absorption showed no variation between IR spectra acquired under dry‐air purge at 25 °C and under vacuum at 25 °C to ?180 °C. Collectively, data from the smectite samples show that the precise center wavelength of the characteristic ~3.05 μm v3 absorption in NH4 is variable and is likely related to the degree of hydrogen bonding of NH4‐H2O complexes. Comparison with Dawn VIR spectra indicates that the hypothesis of Mg‐saponite as the ammonium carrier phase is the simplest explanation for observed data, and that Ceres dark materials may be like Cold Bokkeveld or Tagish Lake but with proportionally more Mg‐smectite.  相似文献   

16.
The space velocities and Galactic orbital elements of stars calculated from the currently available high-accuracy observations in our compiled catalog of spectroscopic magnesium abundances in dwarfs and subgiants in the solar neighborhood are used to identify thick-disk objects. We analyze the relations between chemical, spatial, and kinematic parameters of F–G stars in the identified subsystem. The relative magnesium abundances in thick-disk stars are shown to lie within the range 0.0 < [Mg/Fe] < 0.5 and to decrease with increasingmetallicity starting from [Fe/H] ≈ ?1.0. This is interpreted as evidence for a longer duration of the star formation process in the thick disk. We have found vertical gradients in metallicity (gradZ[Fe/H] = ?0.13 ± 0.04 kpc?1) and relative magnesium abundance (gradZ[Mg/Fe] = 0.06 ± 0.02 kpc?1), which can be present in the subsystem only in the case of its formation in a slowly collapsing protogalaxy. However, the gradients in the thick disk disappear if the stars whose orbits lie in the Galactic plane, but have high eccentricities and low azimuthal space velocities atypical of the thin-disk stars are excluded from the sample. The large spread in relative magnesium abundance (?0.3 < [Mg/Fe] < 0.5) in the stars of the metal-poor “tail” of the thick disk, which constitute ≈8% of the subsystem, can be explained in terms of their formation inside isolated interstellar clouds that interacted weakly with the matter of a single protogalactic cloud. We have found a statistically significant negative radial gradient in relative magnesium abundance in the thick disk (gradR[Mg/Fe] = ?0.03 ± 0.01 kpc? 1) instead of the expected positive gradient. The smaller perigalactic orbital radii and the higher eccentricities for magnesium-richer stars, which, among other stars, are currently located in a small volume of the Galactic space near the Sun, are assumed to be responsible for the gradient inversion. A similar, but statistically less significant inversion is also observed in the subsystem for the radial metallicity gradient.  相似文献   

17.
Pieces of high-silica, natural glass (Libyan Desert Glass), found on the desert surface of western Egypt, have been treated as an enigma for 50 years although it is virtually certain they are similar to tektites in being impact-derived products. New major element analyses of four Libyan Desert Glass specimens agree extremely well with the only other recent analysis and demonstrate that the original bulk analyses reported by Spencer (1939) are in error. The five modern analyses define a very tight chemical range for SiO2 (97.38–98.25 wt %), Al2O3 (1.16–2.26 wt %), total Fe (0.15–0.60 wt % as Fe2O3) and TiO2 (0.13–0.19 wt %). Measurable MgO (0.04–0.20 wt %) was found in one specimen. No other elements are present in greater than trace amounts. Microprobe analyses show that Al, Fe and Ti are all positively correlated with one another and are almost ubiquitously distributed throughout the glass. They must also have been so distributed in the LDG precursor material as mechanical mixing and elemental diffusion in the short-lived melt were limited. In contrast, Mg is sharply restricted in occurrence and correlates only with Fe, strongly suggesting a precursor Mg-Fe oxide or silicate mineral present as rare, discrete grains. Aside from rare accessory minerals, the parent material was a sand or sandstone composed of quartz grains coated with a mixture of kaolinite, hematite and anatase. This conclusion is based solely on the elemental distribution in the glass but is buttressed by the occurrence of both sand and sandstone, in southwestern Egypt, with the requisite mineralogy. However, mineralogic identity need not, in general, translate to a chemical match and it is entirely possible that the specific sand or sandstone facies involved in the glass formation no longer exists after 28 million years. Consequently, it may well be that evidence other than chemical comparisons will be needed to identify the presently unknown parent crater.  相似文献   

18.
A thermodynamical analysis of the multicomponent system SiTiAlFeMnMgCaNaKPCHO open with respect to CO2, CO, H2O was carried out. Hydration and carbonatization processes are proposed to be geochemical consequences of the hypothesis of quasi-equilibrium conditions between the troposphere and crustal surface rocks. The probable rock-forming hydrated mineral phases are represented by epidote, glaucophane, tremolite, phlogopite, and annite; the carbonatization results in existence of calcite and dolomite as rock-forming minerals of weathered alkaline lavas. The surface rocks are assumed to have high ferric/ferrous iron ratios. The wollastonite equilibrium is rejected as a buffering chemical reaction. Hydrated minerals could be stable at least up to 5-km depths and contribute about 0.1 × 1024 g of H2O whereas about (0.7–0.8) × 1024 g of H2O would be consumed in ferrous iron oxidation with concomitant hydrogen dissipation. The distribution of H2O in the outer planetary shells is possibly a function of their temperatures.  相似文献   

19.
We used chemical equilibrium calculations to model thermal outgassing of ordinary chondritic material as a function of temperature, pressure, and bulk composition and use our results to discuss outgassing on asteroids and the early Earth. The calculations include ∼1000 solids and gases of the elements Al, C, Ca, Cl, Co, Cr, F, Fe, H, K, Mg, Mn, N, Na, Ni, O, P, S, Si, and Ti. The major outgassed volatiles from ordinary chondritic material are CH4, H2, H2O, N2, and NH3 (the latter at conditions where hydrous minerals form). Contrary to widely held assumptions, CO is never the major C-bearing gas during ordinary chondrite metamorphism. The calculated oxygen fugacity (partial pressure) of ordinary chondritic material is close to that of the quartz-fayalite-iron (QFI) buffer. Our results are insensitive to variable total pressure, variable volatile element abundances, and kinetic inhibition of C and N dissolution in Fe metal. Our results predict that Earth's early atmosphere contained CH4, H2, H2O, N2, and NH3; similar to that used in Miller—Urey synthesis of organic compounds.  相似文献   

20.
Abstract— We performed a systematic high‐precision secondary ion mass spectrometry 26Al‐26Mg isotopic study for 11 ferromagnesian chondrules from the highly unequilibrated ordinary chondrite Bishunpur (LL3.1). The chondrules are porphyritic and contain various amounts of olivine and pyroxene and interstitial plagioclase and/or glass. The chemical compositions of the chondrules vary from FeO‐poor to FeO‐rich. Eight chondrules show resolvable 26Mg excesses with a maximum δ26Mg of ?1% in two chondrules. The initial 26Al/27Al ratios inferred for these chondrules range between (2.28 ± 0.73) × 10?5 to (0.45 ± 0.21) × 10?5. Assuming a homogeneous distribution of Al isotopes in the early solar system, this range corresponds to ages relative to CAIs between 0.7 ± 0.2 Ma and 2.4+0.7?0.4 Ma. The inferred total span of the chondrule formation ages is at least 1 Ma, which is too long to form chondrules by the X‐wind. The initial 26Al/27Al ratios of the chondrules are found to correlate with the proportion of olivine to pyroxene suggesting that olivine‐rich chondrules formed earlier than pyroxene‐rich chondrules. Though we do not have a completely satisfactory explanation of this correlation we tentatively interpret it as a result of evaporative loss of Si from earlier generations of chondrules followed by addition of Si to the precursors of later generation chondrules.  相似文献   

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