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1.
Chondrules in E3 chondrites differ from those in other chondrite groups. Many contain near-pure endmember enstatite (Fs<1). Some contain Si-bearing FeNi metal, Cr-bearing troilite, and, in some cases Mg, Mn- and Ca-sulfides. Olivine and more FeO-rich pyroxene grains are present but much less common than in ordinary or carbonaceous chondrite chondrules. In some cases, the FeO-rich grains contain dusty inclusions of metal. The oxygen three-isotope ratios (δ18O, δ17O) of olivine and pyroxene in chondrules from E3 chondrites, which are measured using a multi-collection SIMS, show a wide range of values. Most enstatite data plots on the terrestrial fractionation (TF) line near whole rock values and some plot near the ordinary chondrite region on the 3-isotope diagram. Pyroxene with higher FeO contents (∼2-10 wt.% FeO) generally plots on the TF line similar to enstatite, suggesting it formed locally in the EC (enstatite chondrite) region and that oxidation/reduction conditions varied within the E3 chondrite chondrule-forming region. Olivine shows a wide range of correlated δ18O and δ17O values and data from two olivine-bearing chondrules form a slope ∼1 mixing line, which is approximately parallel to but distinct from the CCAM (carbonaceous chondrite anhydrous mixing) line. We refer to this as the ECM (enstatite chondrite mixing) line but it also may coincide with a line defined by chondrules from Acfer 094 referred to as the PCM (Primitive Chondrite Mineral) line (Ushikubo et al., 2011). The range of O isotope compositions and mixing behavior in E3 chondrules is similar to that in O and C chondrite groups, indicating similar chondrule-forming processes, solid-gas mixing and possibly similar 16O-rich precursors solids. However, E3 chondrules formed in a distinct oxygen reservoir.Internal oxygen isotope heterogeneity was found among minerals from some of the chondrules in E3 chondrites suggesting incomplete melting of the chondrules, survival of minerals from previous generations of chondrules, and chondrule recycling. Olivine, possibly a relict grain, in one chondrule has an R chondrite-like oxygen isotope composition and may indicate limited mixing of materials from other reservoirs. Calcium-aluminum-rich inclusions (CAIs) in E3 chondrites have petrologic characteristics and oxygen isotope ratios similar to those in other chondrite groups. However, chondrules from E3 chondrites differ markedly from those in other chondrite groups. From this we conclude that chondrule formation was a local event but CAIs may have all formed in one distinct place and time and were later redistributed to the various chondrule-forming and parent body accretion regions. This also implies that transport mechanisms were less active at the time of and following chondrule formation.  相似文献   

2.
Intrinsic oxygen-fugacity (fO2) measurements were made on five ordinary chondrites, a carbonaceous chondrite, an enstatite chondrite, a pallasite, and a tektite. Results are of the form of linear log fO2 ? 1T plots. Except for the enstatite chondrite, measured results agree well with calculated estimates by others.The tektite produced fO2 values well below the range measured for terrestrial and lunar rocks. The lowpressure atmospheric regime that is reported to follow large terrestrial explosions, coupled with a very high temperature, could produce glass with fO2 in the range measured.The meteorite Salta (pallasite) has low fO2 and lies close to Hvittis (E6). Unlike the other samples, results for Salta do not parallel the iron-wüstite buffer, but are close to the fayalite-quartz-iron buffer in slope.Minor reduction by graphite appears to have taken place during metamorphism of ordinary chondrites. fO2 values of unequilibrated chondrites show large scatter during early heating suggesting that the constituent phases were exposed to a range of fO2 conditions. The samples equilibrated with respect to fO2 in relatively short time on heating. Equilibration with respect to fO2 in ordinary chondrites takes place between grades 3 and 4 of metamorphism. Application of P ? T ? fO2 relations in the system C-CO-CO2 indicates that the ordinary chondrites were metamorphosed at pressures of 3–20 bars, as it appears that they lay on the graphite surface.A steep positive thermal gradient in a meteorite parent body lying at the graphite surface will produce thin reduced exterior, an oxidized near-surface layer, and an interior that is increasingly reduced with depth; a shallow thermal gradient will produce the reverse. A body heated by accretion on the outside will have a reduced exterior and oxidized interior. Meteorites from the same parent body clearly are not required to have similar redox states.  相似文献   

3.
Samples are available from 37 stony meteorites falling in China. Twenty-two chondrites are examined in terms of chemical and mineral compositions, cosmogenic nuclides, formation and exposure ages, impact effect and chondrule textures. On the basis of chemical-petrologic features these chondrites are classified asE 4 (Qingzhen),H 5 (Jilin, Changde, Shuangyang, Anlong, Xinyi and Yangjang),L 6 (Renqiu, Junan, Heze, Rugao and Nei Monggol) andLL 6 (Dongtai). E 4 is characterized by high iron and sulfur, with the former occurring mainly as Feo and FeS. FromH 5 throughH 6 toLL 6, iron and nickel decrease gradually while FeO and the ratio of Fe silicate to total iron increase gradually. indicating a general increase in the orderE-H-L-LL in the degree of oxidation at the time of formation. E 4 consists mainly of enstatite and, to much less extent, free SiO2 but olivine is hardly to be found. The olivine proportions amount to 29.07, 41.98 and 51.36 percent inH 5,L 6 andLL 6 respectively, with Fa increasing from 17 to 27 percent. Recrystallization has been noticed to different degrees inH 4,H 5,L 6 andLL 6 chondrites. The extent to which the original structure disappears and the boundaries of chondrules become indistinct decreases from type 6 through type 5 to type 4, reflecting different degrees of thermal metamorphism. Major minerals in the meteorites all exhibit signs of low to medium shock metamorphism. Specific activity, depth effect and orbit effect are also measured on some chondrites that have fallen in recent years and some new information has been obtained with respect to the orbit and source region for meteorite parent bodies in space. This results show that the environment of formation ofE group may be nearer to Mars than that ofO group. Each chemical group of chondrites has its own evolutionary history, and chondritets of different chemical groups may have originated from parent bodies of different compositions. Or owing to the differentiation caused by thermal melamorphism, various kinds of meteorites may be derived from a common parent body. From this argument it is suggested that five stages may be recognized during the formation process of chondrites.  相似文献   

4.
Initial 129I/127I values (I-Xe ages) have been obtained for individual mineralogically characterized chondrules and interchondrule matrix from the enstatite chondrites Qingzhen (EH3) and Kota Kota (EH3). In view of the absence of aqueous alteration and the low-peak metamorphic temperatures experienced by these meteorites, we suggest that the I-Xe ages for the chondrules record the event in which they were formed. These ages are within the range recorded for chondrules from ordinary chondrites, demonstrating that chondrules formed during the same time interval in the source regions of both ordinary chondrites and enstatite chondrites. The timing of this chondrule-forming episode or episodes brackets the I-Xe closure age of planetesimal bodies such as the Shallowater aubrite parent body. Although chondrule formation need not have occurred close to planetesimals, the existence of planetesimals at the same time as chondrule formation provides constraints on models of this process. Whichever mechanisms are proposed to form and transport chondrules, they must be compatible with models of the protosolar nebula which predict the formation of differentiated bodies on the same timescale at the same heliocentric distance.  相似文献   

5.
Chondrules from the Semarkona (LL3.0) chondrite show refractory and common lithophile fractionation trends similar to those observed among the chondrite groups. It appears that chondrules are mixtures of a small number of pre-existing solid components, and we infer that chondrule precursor materials were related to the nebular components involved in the lithophile element fractionations recognized in ordinary chondrites. Compositional trends among the chondrules can be used to deduce the compositions of these components.We use instrumental neutron activation analysis to measure many (~20) of the lithophile elements in 30 chondrules. The amounts of oxidized iron were calculated from other compositional parameters; concentrations of Si were estimated using mass-balance considerations. The data were corrected for the diluting effects of non-lithophile constituents. Plots of lithophile elements versus a reference refractory element such as Al show that there were two major chondrule silicate precursor components: a refractory, olivine-rich, FeO-free one, and a non-refractory, SiO2-, FeO-rich one.The refractory component probably forms from olivine-enriched condensates formed above the condensation temperature of enstatite. The non-refractory component must have formed from fine-grained materials that were able to equilibrate down to lower nebular temperatures. Chondrite matrix may have had an origin similar to that of the non-refractory material, and constitutes a third lithophile-bearing component that took part in chondrite fractionation processes. The low abundance of refractories and Mg in ordinary and enstatite chondrites was produced by the loss of materials having a higher refractory-element/Mg ratio than that in the refractory component of chondrules.  相似文献   

6.
The oxygen-isotope compositions (obtained by laser fluorination) of hand-picked separates of isolated forsterite, isolated olivine and chondrules from the Tagish Lake carbonaceous chondrite describe a line (δ17O = 0.95 * δ18O − 3.24; R2 = 0.99) similar to the trend known for chondrules from other carbonaceous chondrites. The isolated forsterite grains (Fo99.6-99.8; δ18O = −7.2‰ to −5.5‰; δ17O = −9.6‰ to −8.2‰) are more 16O-rich than the isolated olivine grains (Fo39.6-86.8; δ18O = 3.1‰ to 5.1‰; δ17O = −0.3‰ to 2.2‰), and have chemical and isotopic characteristics typical of refractory forsterite. Chondrules contain olivine (Fo97.2-99.8) with oxygen-isotope compositions (δ18O = −5.2‰ to 5.9‰; δ17O = −8.1‰ to 1.2‰) that overlap those of isolated forsterite and isolated olivine. An inverse relationship exists between the Δ17O values and Fo contents of Tagish Lake isolated forsterite and chondrules; the chondrules likely underwent greater exchange with 16O-poor nebular gases than the forsterite. The oxygen-isotope compositions of the isolated olivine grains describe a trend with a steeper slope (1.1 ± 0.1, R2 = 0.94) than the carbonaceous chondrite anhydrous mineral line (CCAMslope = 0.95). The isolated olivine may have crystallized from an evolving melt that exchanged with 16O-poor gases of somewhat different composition than those which affected the chondrules and isolated forsterite. The primordial components of the Tagish Lake meteorite formed under conditions similar to other carbonaceous chondrite meteorite groups, especially CMs. Its alteration history has its closest affinities to CI carbonaceous chondrites.  相似文献   

7.
The carbon isotopic composition of the total carbon in the enstatite chondrites Indarch, Abee, St. Marks, Pillistfer, Hvittis and Daniel's Kuil and the enstatite achondrite Cumberland Falls has been measured. The empirical relationhip between carbon isotopic composition and total carbon content is distinct from that of carbonaceous and ordinary chondrites. Within the enstatite chondrite group the average 13C content increases with petrographic type: E4 < E5 < E6. Daniel's Kuil shows the largest 13C enrichment in the bulk carbon of any meteorite. The carbon isotopic composition is most clearly correlated with the abundance of the elements Zn, Cd and In. Insofar as these elements may hold the key to the understanding of enstatite chondrites, more detailed combined carbon isotope and trace element studies of these meteorites will play an important role in the deciphering of their history.  相似文献   

8.
Enstatite-rich meteorites include EH and EL chondrites, rare ungrouped enstatite chondrites, aubrites, a few metal-rich meteorites (possibly derived from the mantle of the aubrite parent body), various impact-melt breccias and impact-melt rocks, and a few samples that may be partial-melt residues ultimately derived from enstatite chondrites. Members of these sets of rocks exhibit a wide range of impact features including mineral-lattice deformation, whole-rock brecciation, petrofabrics, opaque veins, rare high-pressure phases, silicate darkening, silicate-rich melt veins and melt pockets, shock-produced diamonds, euhedral enstatite grains, nucleation of enstatite on relict grains and chondrules, low MnO in enstatite, high Mn in troilite and oldhamite, grains of keilite, abundant silica, euhedral graphite, euhedral sinoite, F-rich amphibole and mica, and impact-melt globules and spherules. No single meteorite possesses all of these features, although many possess several. Impacts can also cause bulk REE fractionations due to melting and loss of oldhamite (CaS) – the main REE carrier in enstatite meteorites. The Shallowater aubrite can be modeled as an impact-melt rock derived from a large cratering event on a porous enstatite chondritic asteroid; it may have been shock melted at depth, slowly cooled and then excavated and quenched. Mount Egerton may share a broadly similar shock and thermal history; it could be from the same parent body as Shallowater. Many aubrites contain large pyroxene grains that exhibit weak mosaic extinction, consistent with shock-stage S4; in contrast, small olivine grains in some of these same aubrites have sharp or undulose extinction, consistent with shock stage S1 to S2. Because elemental diffusion is much faster in olivine than pyroxene, it seems likely that these aubrites experienced mild post-shock annealing, perhaps due to relatively shallow burial after an energetic impact event. There are correlations among EH and EL chondrites between petrologic type and the degree of shock, consistent with the hypothesis that collisional heating is mainly responsible for enstatite-chondrite thermal metamorphism. Nevertheless, the apparent shock stages of EL6 and EH6 chondrites tend to be lower than EL3-5 and EH3-5 chondrites, suggesting that the type-6 enstatite chondrites (many of which possess impact-produced features) were shocked and annealed. The relatively young Ar–Ar ages of enstatite chondrites record heating events that occurred long after any 26Al that may have been present initially had decayed away. Impacts remain the only plausible heat source at these late dates. Some enstatite meteorites accreted to other celestial bodies: Hadley Rille (EH) was partly melted when it struck the Moon; Galim (b), also an EH chondrite, was shocked and partly oxidized when it accreted to the LL parent asteroid. EH, EL and aubrite-like clasts also occur in the polymict breccias Kaidun (a carbonaceous chondrite) and Almahata Sitta (an anomalous ureilite). The EH and EL clasts in Kaidun appear unshocked; some clasts in Almahata Sitta may have been extensively shocked on their parent bodies prior to being incorporated into the Almahata Sitta host.  相似文献   

9.
The carbonaceous chondrites are intriguing and unique in the sense that they are the only rocks that provide pristine records of the early solar nebular processes. We report here results of a detailed mineralogical, chemical, amino acid and isotopic studies of a recently observed fall at Mukundpura, near Jaipur in Rajasthan, India. Abundance of olivines in this meteorite is low and of serpentine minerals is high. FeO/SiO_2 = 1.05 in its Poorly Characterized Phases(PCP) is similar to that observed in other CM2.0 chondrites. The water content of ～9.8 wt.% is similar to that found in many other CM chondrites.Microscopic examination of matrix shows that its terrestrial weathering grade is WO but aqueous parent body alteration is high, as reflected in low abundance of identifiable chondrules and abundant remnants of chondrules(～7%). Thus, most of the chondrules formed initially have been significantly altered or dissolved by aqueous alterations on their parent bodies. The measured bulk carbon(2.3%) and nitrogen content and their isotopic(δ13C =-5.5‰, δ15N = 23.6%0) composition is consistent with CM2.0 classification probably bordering CM1. Several amino acids such as Alanine, Serine, Proline, Valine, Threonine,Leucine, Isoleucine, Asparagine and Histamine are present. Tyrosine and Tryptophan may occur in trace amounts which could not be precisely determined. All these data show that Mukundpura chondrite lies at the boundary of CM2.0 and CM1 type carbonaceous chondrites making it one of the most primitive chondrites.  相似文献   

10.
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   

11.
The Bovedy L-group chondrite contains a light-colored poikilitic lithic fragment with olivine, low-Ca pyroxene and kamacite compositions characteristic of porphyritic chondrules from unequilibrated ordinary chondrites. Its texture, compositional similarities to porphyritic chondrules, and low Na2O, K2O and P2O5 content indicate that the fragment represents a solidified, slightly fractionated impact melt formed from a source that was rich in porphyritic chondrules. The fragment is heterogeneous, with a progressive increase in the bulk MgOFeO ratio and in MgO content of olivines and low-Ca pyroxenes across its length. 39Ar40Ar analyses of the fragment and host indicate that the meteorite experienced extensive degassing due to reheating. The approximate age of 0.5–0.94 Byr dates the reheating event and not the formation of the lithic fragment or the Bovedy breccia. This reheating event renders the fragment's and host's metallographic cooling rate of ~ 5 C/Myr (through 500°C) imprecise. However, the absence of martensite and the presence of kamacite. zoned taenite and tetrataenite in the fragment and host are consistent with such slow cooling through 500°C. This cooling rate must have resulted from burial of the fragment-host assemblage beneath insulating material on the Bovedy parent body. If the thermal diffusivity (κ) of this overburden was approximately comparable to that of the lunar regolith (10?4cm2/sec), then the fragment was buried at a depth ≌ 6.5 km; if K = 10?2 cm2/sec (similar to chondritic material), then the fragment was buried at a depth ?65 km.  相似文献   

12.
The R chondrite meteorite LaPaz Icefield (LAP) 04840 is unique among metamorphosed, non-carbonaceous chondrites in containing abundant OH-bearing silicate minerals: ∼13% ferri-magnesiohornblende and ∼0.4% phlogopite by volume. Other minerals include olivine (Fo62), orthopyroxene (En69Fs30Wo1), albite (An8Ab90Or2), magnetite, pyrrhotite, pentlandite, and apatite. Ferromagnesian minerals are rich in Fe3+, as determined by Mössbauer spectrometry and electron microprobe chemical analyses. Fe3+/Fetot values are olivine ?5%, amphibole 80%, phlogopite 65%, and magnetite 42%. Mineral compositions are nearly constant across grains and the section, except for a small variability in amphibole compositions reflecting the edenite exchange couple (ANa + IVAl ↔ A□ + Si). These mineral compositions, the absence of Fe-Ni metal, and the oxygen isotope data support its classification as an R (Rumuruti) chondrite. LAP 04840 is classified as petrologic grade 5, based on the chemical homogeneity of its minerals, and the presence of distinctly marked chondrules and chondrule fragments in a fine-grained crystalline matrix. The mineral assemblage of LAP 04840 allows calculation of physical and chemical conditions at the peak of its metamorphism: T = 670 ± 60 °C from a amphibole-plagioclase thermometer; PH2O between 250 and 500 bars as constrained by the assemblage phlogopite + orthopyroxene + olivine + feldspar and the absence of diopside; PCO2 unconstrained; fO2 at QFM + 0.5 log units; . The hydrogen in LAP 04840 is very heavy, an average δD value of +3660 ± 75‰ in the magnesiohornblende. Only a few known sources of hydrogen have such high δD and are suitable sources for LAP 04840: ordinary chondrite phyllosilicates (as in the Semarkona chondrite), and insoluble organic matter (IOM) in ordinary chondrites and CR chondrites. Hydrogen from the IOM could have been released by oxidation, and then reacted with an anhydrous R chondrite (at high temperature), but it is not clear whether this scenario is correct.  相似文献   

13.
The Varre-Sai meteorite fell along the border of the states of Espirito Santo and Rio de Janeiro, Brazil; on 19 June 2010 at 5:40 pm. Petrography and X-ray powder diffraction (XRD) indicate that the rock is an L5 S4 chondrite, with blastoporphyritic texture that has not been previously described. Geochemical data based on major and rare-earth elements (REEs) show that Varre-Sai is highly similar to the other L chondrites. In Harker diagrams, Varre-Sai, L, and LL chondrites form a single group, suggesting no significant chemical differences between them and contributing to the long-standing debate of whether LL chondrites form a distinct group or whether they are a subset of the L group. Harker diagrams also define a trend from E to H and L/LL chondrites, similar to the cosmochemical trends suggested by other authors. The behaviour of Fe2O3t and NiO indicates a relationship with Fe-Ni alloys, and their trend in the diagram suggests some chemical differentiation in the ordinary chondrite parental bodies. The REE content in Varre-Sai, normalized to C chondrites, falls in the field of L chondrites and others, but with slight REE enrichment. The chemical differences in chondrites, mainly in REEs, Fe2O3t and NiO could be alternatively interpreted as variations in the inherited agglutinated materials as chondrules, Ca–Al-rich inclusions and Fe–Ni nodules.  相似文献   

14.
Forty-six reversed determinations of the Al2O3content of enstatite in equilibrium with garnet were made in the P/T range 15–40 kbar/900–1,600° C in the MgO-Al2O3-SiO2 system. Starting materials were mixtures of synthetic pyrope+Al-free enstatite and pyrope+enstatite (5–12% Al2O3). Al2O3 contents in reversal run pairs closely approached common values from both the high- and low-Al sides. Most experiments were done in a piston-cylinder device using a NaCl medium; some runs at very high temperatures were made in pyrex/NaCl or pyrex/talc assemblies. The measured enstatite compositions, expressed as mole fractions of Mg2(MgAl)(AlSi3)O12(X Opy En ) were fitted by a Monte-Carlo method to the equilibrium condition: $$\begin{gathered} \Delta H_{970}^0 - 970\Delta S_{970}^0 \hfill \\ + \mathop \smallint \limits_1^P \Delta V_{970}^0 dP - \mathop \smallint \limits_{970}^T \Delta S_T^0 dT + RT\ln X_{Opy}^{En} = 0 \hfill \\ \end{gathered}$$ where the best fit parameters of ΔH, ΔS and ΔV (1 bar, 970 K) for the reaction pyrope=opy are 2,040 cal/mol, 2.12 eu and 9.55 cc/mol. In addition to the determination of Al2O3 contents of enstatite, the univariant reaction pyrope+forsterite=enstatite+spinel was reversibly located in the range 1,100–1,400°C. A “best-fit” line passes through 22, 22.5 and 25 kbar at 1,040, 1,255 and 1,415°C, respectively. Our results for the univariant reaction are in agreement with previous studies of MacGregor (1974) and Haselton (1979). However, comparison of the experimentally determined curve with thermochemical calculations suggests that there may be a small error in the tabulated ΔH f(970,1) 0 value for enstatite. A value of?8.32 rather than?8.81 kcal/mole (Charlu et al. 1975) is consistent with the present data. Application of garnet-enstatite-spinel-forsterite equilibria to natural materials is fraught with difficulties. The effects of nonternary components are poorly understood, and the low solubilities of Al2O3 in enstatite under most geologically reasonable conditions make barometric or thermometric calculations highly sensitive. More detailed studies, including reversed determinations in low-friction assemblies, are sorely needed before the effects of important diluents such as Fe, Ca and Cr can be fully understood.  相似文献   

15.
An Fe isotope study of ordinary chondrites   总被引：3，自引：0，他引：3  
The Fe isotope composition of ordinary chondrites and their constituent chondrules, metal and sulphide grains have been systematically investigated. Bulk chondrites fall within a restricted isotopic range of <0.2‰ δ56Fe, and chondrules define a larger range of >1‰ (−0.84‰ to 0.21‰ relative to the IRMM-14 Fe standard). Fe isotope compositions do not vary systematically with the very large differences in total Fe concentration, or oxidation state, of the H, L, and LL chondrite classes. Similarly, the Fe isotope compositions of chondrules do not appear to be determined by the H, L or LL classification of their host chondrite. This may support an origin of the three ordinary chondrite groups from variable accretion of identical Fe-bearing precursors.A close relationship between isotopic composition and redistribution of Fe during metamorphism on ordinary chondrite parent bodies was identified; the largest variations in chondrule compositions were found in chondrites of the lowest petrologic types. The clear link between element redistribution and isotopic composition has implications for many other non-traditional isotope systems (e.g. Mg, Si, Ca, Cr). Isotopic compositions of chondrules may also be determined by their melting history; porphyritic chondrules exhibit a wide range in isotope compositions whereas barred olivine and radial pyroxene chondrules are generally isotopically heavier than the ordinary chondrite mean. Very large chondrules preserve the greatest heterogeneity of Fe isotopes.The mean Fe isotope composition of bulk ordinary chondrites was found to be −0.06‰ (±0.12‰ 2 SD); this is isotopically lighter than the terrestrial mean composition and all other published non-chondritic meteorite suites e.g. lunar and Martian samples, eucrites, pallasites, and irons. Ordinary chondrites, though the most common meteorites found on Earth today, were not the sole building blocks of the terrestrial planets.  相似文献   

16.
In the Piancaldoli LL3 chondrite, we found a mm-sized clast containing ~100 chondrules 0.2–64 μm in apparent diameter (much smaller than any previously reported) that are all of the same textural type (radial pyroxene; FS1–17). This clast, like other type 3 chondrites, has a fine-grained Ferich opaque silicate matrix, sharply defined chondrules, abundant low-Ca clinopyroxene and minor troilite and Si- and Cr-bearing metallic Fe,Ni. However, the very high modal matrix abundance (63 ± 8 vol. %), unique characteristics of the chondrules, and absence of microscopically-observable olivine indicate that the clast is a new kind of type 3 chondrite. Most chondrules have FeO-rich edges, and chondrule size is inversely correlated with chondrule-core FeO concentration (the first reported correlation of chondrule size and composition). Chondrules acquired Fe by diffusion from Fe-rich matrix material during mild metamorphism, possibly before final consolidation of the rock. Microchondrules (those chondrules ? 100 μm in diameter) are also abundant in another new kind of type 3 chondrite clast in the Rio Negro L chondrite regolith breccia. In other type 3 chondrite groups, microchondrule abundance appears to be anticorrelated with mean chondrule size, viz. 0.02–0.04 vol. % in H and CO chondrites and ?0.006 vol. % in L, LL, and CV chondrites.Microchondrules probably formed by the same process that formed normal-sized droplet chondrules: melting of pre-existing dustballs. Because most compound chondrules in the clast and other type 3 chondrites formed by collisions between chondrules of the same textural type, we suggest that dust grains were mineralogically sorted in the nebula before aggregating into dustballs. The sizes of compound chondrules and chondrule craters, which resulted from collisions of similarly-sized chondrules while they were plastic, indicate that size-sorting (of dustballs) occurred before chondrule formation, probably by aerodynamic processes in the nebula. We predict that other kinds of type 3 chondrites exist which contain chondrule abundances, size-ranges and proportions of textural types different from known chondrite groups.  相似文献   

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It has been recently suggested that (1) CH chondrites and the CBb/CH-like chondrite Isheyevo contain two populations of chondrules formed by different processes: (i) magnesian non-porphyritic (cryptocrystalline and barred) chondrules, which are similar to those in the CB chondrites and formed in an impact-generated plume of melt and gas resulted from large-scale asteroidal collision, and (ii) porphyritic chondrules formed by melting of solid precursors in the solar nebula. (2) Porphyritic chondrules in Isheyevo and CH chondrites are different from porphyritic chondrules in other carbonaceous chondrites ( [Krot et al., 2005], [Krot et al., 2008a] and [Krot et al., 2008b]). In order to test these hypotheses, we measured in situ oxygen isotopic compositions of porphyritic (magnesian, Type I and ferroan, Type II) and non-porphyritic (magnesian and ferroan cryptocrystalline) chondrules from Isheyevo and CBb chondrites MAC 02675 and QUE 94627, paired with QUE 94611, using a Cameca ims-1280 ion microprobe.On a three-isotope oxygen diagram (δ17O vs. δ18O), compositions of chondrules measured follow approximately slope-1 line. Data for 19 magnesian cryptocrystalline chondrules from Isheyevo, 24 magnesian cryptocrystalline chondrules and 6 magnesian cryptocrystalline silicate inclusions inside chemically-zoned Fe,Ni-metal condensates from CBb chondrites have nearly identical compositions: Δ17O = −2.2 ± 0.9‰, −2.3 ± 0.6‰ and −2.2 ± 1.0‰ (2σ), respectively. These observations and isotopically light magnesium compositions of cryptocrystalline magnesian chondrules in CBb chondrites (Gounelle et al., 2007) are consistent with their single-stage origin, possibly as gas-melt condensates in an impact-generated plume. In contrast, Δ17O values for 11 Type I and 9 Type II chondrules from Isheyevo range from −5‰ to +4‰ and from −17‰ to +3‰, respectively. In contrast to typical chondrules from carbonaceous chondrites, seven out of 11 Type I chondrules from Isheyevo plot above the terrestrial fractionation line. We conclude that (i) porphyritic chondrules in Isheyevo belong to a unique population of objects, suggesting formation either in a different nebular region or at a different time than chondrules from other carbonaceous chondrites; (ii) Isheyevo, CB and CH chondrites are genetically related meteorites: they contain non-porphyritic chondrules produced during the same highly-energetic event, probably large-scale asteroidal collision; (iii) the differences in mineralogy, petrography, chemical and whole-rock oxygen isotopic compositions between CH and CB chondrites are due to various proportions of the nebular and the impact-produced materials.  相似文献   

18.
The enstatite chondrites formed under highly reducing (and/or sulfidizing) conditions as indicated by their mineral assemblages and compositions, which are sharply different from those of other chondrite groups. Enstatite is the major silicate mineral. Kamacite is Si-bearing and the enstatite chondrites contain a wide variety of monosulfide minerals that are not present in other chondrite groups. The unequilibrated enstatite chondrites are comprised of two groups (EH3 and EL3) and one anomalous member (LEW 87223), which can be distinguished by differences in their mineral assemblages and compositions. EH3 chondrites have >1.8 wt.% Si in their kamacite and contain the monosulfide niningerite (MgS), whereas EL3 chondrites have less than 1.4 wt.% Si in their kamacite and contain the monosulfide alabandite (MnS). The distinct mineralogies, compositions and textures of E3 chondrites make comparisons with ordinary chondrites (OCs) and carbonaceous chondrites (CCs) difficult, however, a range of recrystallization features in the E3s are observed, and some may be as primitive as type 3.1 OCs and CCs. Others, especially the EL3 chondrites, may have been considerably modified by impact processes and their primary textures disturbed. The chondrules in E3 chondrites, although texturally similar to type I pyroxene-rich chondrules, are sharply different from chondrules in other chondrite groups in containing Si-bearing metal, Ca- and Mg–Mn-rich sulfides and silica. This indicates formation in a reduced nebular environment separate from chondrules in other chondrites and possibly different precursor materials. Additionally the oxygen isotope compositions of E3 chondrules indicate formation from a unique oxygen reservoir. Although the abundance, size distribution, and secondary alteration minerals are not always identical, CAIs in E3 chondrites generally have textures, mineral assemblages and compositions similar to those in other groups. These observations indicates that CAIs in O, C and E chondrites all formed in the reservoir under similar conditions, and were redistributed to the different chondrite accretion zones, where the secondary alteration took place. Thus, chondrule formation was a local process for each particular chondrite group, but all CAIs may have formed in the similar nebular environment. Lack of evidence of water (hydrous minerals), and oxygen isotope compositions similar to Earth and Moon suggest formation of the E chondrites in the inner solar system and make them prime candidates as building blocks for the inner planets.  相似文献   

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