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51.
The oxygen isotopic distribution in an amoeboid olivine aggregate (AOA), TTA1-02, from the Allende CV3 chondrite has been determined by secondary ion mass spectrometry. The irregular shaped TTA1- 02 (5×3mm) consists mostly of olivine grains of ca. 5μm in diameter. Olivine grains of Mg-rich (Fo95) and Fe-rich (Fo60) composition are in direct contact with each other, with a sharp compositional boundary. Oxygen isotopic compositions of Fe-rich olivine grains are 16O-poor (Δ17O ≅ −5‰), whereas Mg-rich olivine is 16O-rich (Δ17O ≅ −25‰). Several Al-rich inclusions (<ca. 500 μm in diameter) are enclosed by olivine grains in the AOA. Oxygen isotopic compositions of spinel and fassaite in Al-rich inclusions are 16O-rich (Δ17O ≅ −20‰), whereas those of anorthite, nepheline and phyllosilicate are 16O-poor (Δ17O ≅ −5‰). We propose the following sequence of events during the formation of AOAs in the Allende meteorite: 1) Formation of Al-rich inclusions with 16O-rich oxygen isotopic composition; 2) Accretion of Mg-rich olivine grains with 16O-rich oxygen isotopic composition around Al-rich inclusions; 3) Accretion into parent body; and 4) Aqueous alteration in the parent body, which led to crystallization of 16O-poor minerals, Fe-rich olivine, anorthite, nepheline, and phyllosilicate. This is reflecting reactions among primary 16O-rich AOA minerals and aqueous fluid having 16O-poor oxygen isotopic composition. Fe-rich olivine grains precipitated from aqueous fluids, which partially dissolved pre-existing Mg-rich olivine grains. Sintering and Mg-Fe diffusion occurred during thermal metamorphism. Anorthite, nepheline and phyllosilicate in Al-rich inclusions replaced primary anorthite or melilite during the aqueous alteration stage. 相似文献
52.
Peridotites from the Mariana Trough: first look at the mantle beneath an active back-arc basin 总被引:3,自引:0,他引:3
Yasuhiko Ohara Robert J. Stern Teruaki Ishii Hisayoshi Yurimoto Toshitsugu Yamazaki 《Contributions to Mineralogy and Petrology》2002,143(1):1-18
Two dives of the DSV Shinkai 6500 in the Mariana Trough back-arc basin in the western Pacific sampled back-arc basin mantle exposures. Reports of peridotite exposures in back-arc basin setting are very limited and the lack of samples has hindered our understanding of this important aspect of lithospheric evolution. The Mariana Trough is a slow-spreading ridge, and ultramafic exposures with associated gabbro dykes or sills are located within a segment boundary. Petrological data suggest that the Mariana Trough peridotites are moderately depleted residues after partial melting of the upper mantle. Although some peridotite samples are affected by small-scale metasomatism, there is no evidence of pervasive post-melting metasomatism or melt-mantle interaction. Spinel compositions plot in the field for abyssal peridotites. Clinopyroxenes show depletions in Ti, Zr, and REE that are intermediate between those documented for peridotites from the Vulcan and Bouvet fracture zones (the American-Antarctic and Southwest Indian ridges, respectively). The open-system melting model indicates that the Mariana Trough peridotite compositions roughly correspond to theoretical residual compositions after ~7% near-fractional melting of a depleted MORB-type upper mantle with only little melt or fluid/mantle interactions. The low degree of melting is consistent with a low magma budget, resulting in ultramafic exposure. We infer that the mantle flow beneath the Mariana Trough Central Graben is episodic, resulting in varying magma supply rate at spreading segments. 相似文献
53.
Rain‐induced deep‐seated catastrophic rockslides controlled by a thrust fault and river incision in an accretionary complex in the Shimanto Belt,Japan 下载免费PDF全文
To clarify the geological causes of rockslides induced by rainstorms in accretionary complexes, the geology and geomorphology of two large rockslides (volumes > 106 m3) induced by the heavy rainfall of Typhoon Talas in the Shimanto Belt, Kii Mountains, Japan in 2011 are investigated. Our analysis reveals that thrusts with brittle crush zones controlled the occurrence of the rockslides. The properties and distribution of thrusts were poorly constrained before this study. Flooding during the rainstorm removed surface materials along rivers, allowing thorough geological mapping to be performed. Gravitationally deformed slopes were studied using GIS analysis of 1 m digital elevation models (DEMs) and fieldwork, and X‐ray diffraction (XRD) analysis, permeability, and direct shear tests were used to characterize the mineralogy and geotechnical properties of fault gouge. The Kawarabi thrust has a brittle crush zone up to 6 m thick and acts as the sliding surface for both landslides. The thrust dips 34° downslope and is cut by high‐angle faults and joints along one or both sides of each landslide body. Prior to failure, the upper part of the slope contained small scarps, suggesting that the slopes were already gravitationally deformed. The slope instability can be attributed to long‐term river erosion, which has undercut the slope and exposed the thrust at the base of the slope. The groundwater level, monitored in boreholes, suggests that the Kawarabi thrust is a barrier to groundwater flow. The weak and impermeable nature of the thrust played an essential role in the generation of gravitational slope deformation and catastrophic failure during periods of increased rainfall. Thrusts are a common feature of accretionary complexes, including in the Shimanto Belt, and the mechanism of slope failure stated above can be typical of rockslides in accretionary complexes and provide new insights into landslide disaster mitigation. 相似文献
54.
Mineral chemistry and petrogenesis of chromitites from the Khoy ophiolite complex,Northwestern Iran: Implications for aggregation of two ophiolites 下载免费PDF全文
Fatemeh Zaeimnia Ali Kananian Shoji Arai Mirsaleh Mirmohammadi Ali Imamalipour Mohamed Zaki Khedr Makoto Miura Khadidja Abbou‐Kebir 《Island Arc》2017,26(6)
The Khoy ophiolitic complex in Northwestern Iran is a part of the Tethyan ophiolite belt, and is divided into two sections: the Eastern ophiolite in Qeshlaq and Kalavanes (Jurassic–Cretaceous) and the Western ophiolite in Barajouk, Chuchak and Hessar (Late Cretaceous). Our chromitites can be clearly classified into two groups: high‐Al chromitites (Cr# = 0.38–0.44) from the Eastern ophiolite, and high‐Cr chromitites (Cr# = 0.54–0.72) from the Western ophiolite. The chromian spinels in high‐Al chromitite include primary mineral inclusions mainly as Na‐bearing diopside and pargasite with subordinate rutile and their formation was probably related to reaction between a MORB (mid‐ocean‐ridge basalt)‐like melt with depleted harzburgite, possibly in a back‐arc setting. Their host harzburgites contain clinopyroxene with higher contents of Al2O3, Na2O, Cr2O3, and TiO2 relative to Western harzburgites and are possibly residue after moderate partial melting (~15 %) whereas the Western harzburgite is residue after high partial melting (~25 %). The chromian spinel in the Western Khoy chromitites contains inclusions such as clinopyroxene, olivine and platinum group mineral‐bearing sulfides. These Western chromitites were possibly formed at two stages during arc growth and are divided into the moderately high‐Cr# chromitites (Barajouk and Hessar) and the high‐Cr# chromitites (Chuchak A and C). The former crystallized from island‐arc‐tholeiite (IAT) melts during reaction with the host depleted harzburgites, whereas the latter crystallized from boninitic melts (second stage melt) during reaction with highly depleted harzburgite in a supra‐subduction‐zone environment. Based on the mineral chemistry of chromian spinels, pyroxenes, and mineral inclusions, the chromitites and the host peridotites from the Eastern and Western Khoy ophiolites were formed in a back‐arc basin and arc‐related setting, respectively. The Khoy ophiolitic complex is a tectonic aggregate of the two different ophiolites formed in two different tectonic settings at different ages. 相似文献
55.
Mantle peridotites from the Western Pacific 总被引:1,自引:0,他引:1
We review petrographical and petrological characteristics of mantle peridotite xenoliths from the Western Pacific to construct a petrologic model of the lithospheric mantle beneath the convergent plate boundary. The peridotite varies from highly depleted spinel harzburgite of low-pressure origin at the volcanic front of active arcs (Avacha of Kamchatka arc and Iraya of Luzon–Taiwan arc) to fertile spinel lherzolite of high-pressure origin at the Eurasian continental margin (from Sikhote-Alin through Korea to eastern China) through intermediate lherzolite–harzburgite at backarc side of Japan island arcs. Oxygen fugacity recorded by the peridotite xenoliths decreases from the frontal side of arc to the continental margin. The sub-arc type peridotite is expected to exist beneath the continental margin if accretion of island arc is one of the important processes for continental growth. Its absence suggests replacement by the continental lherzolite at the region of backarc to continental margin. Asthenospheric upwelling beneath the continental region, which has frequently occurred at the Western Pacific, has replaced depleted sub-cratonic peridotite with the fertile spinel lherzolite. Some of these mantle diapirs had opened backarc basins and strongly modified the lithospheric upper mantle by metasomatism and formation of Group II pyroxenites. 相似文献
56.
Uranyl adsorption and surface speciation at the imogolite-water interface: Self-consistent spectroscopic and surface complexation models 总被引:1,自引:0,他引:1
Macro- and molecular-scale knowledge of uranyl (U(VI)) partitioning reactions with soil/sediment mineral components is important in predicting U(VI) transport processes in the vadose zone and aquifers. In this study, U(VI) reactivity and surface speciation on a poorly crystalline aluminosilicate mineral, synthetic imogolite, were investigated using batch adsorption experiments, X-ray absorption spectroscopy (XAS), and surface complexation modeling. U(VI) uptake on imogolite surfaces was greatest at pH ∼7-8 (I = 0.1 M NaNO3 solution, suspension density = 0.4 g/L [U(VI)]i = 0.01-30 μM, equilibration with air). Uranyl uptake decreased with increasing sodium nitrate concentration in the range from 0.02 to 0.5 M. XAS analyses show that two U(VI) inner-sphere (bidentate mononuclear coordination on outer-wall aluminol groups) and one outer-sphere surface species are present on the imogolite surface, and the distribution of the surface species is pH dependent. At pH 8.8, bis-carbonato inner-sphere and tris-carbonato outer-sphere surface species are present. At pH 7, bis- and non-carbonato inner-sphere surface species co-exist, and the fraction of bis-carbonato species increases slightly with increasing I (0.1-0.5 M). At pH 5.3, U(VI) non-carbonato bidentate mononuclear surface species predominate (69%). A triple layer surface complexation model was developed with surface species that are consistent with the XAS analyses and macroscopic adsorption data. The proton stoichiometry of surface reactions was determined from both the pH dependence of U(VI) adsorption data in pH regions of surface species predominance and from bond-valence calculations. The bis-carbonato species required a distribution of surface charge between the surface and β charge planes in order to be consistent with both the spectroscopic and macroscopic adsorption data. This research indicates that U(VI)-carbonato ternary species on poorly crystalline aluminosilicate mineral surfaces may be important in controlling U(VI) mobility in low-temperature geochemical environments over a wide pH range (∼5-9), even at the partial pressure of carbon dioxide of ambient air (pCO2 = 10−3.45 atm). 相似文献
57.
John T. WASSON Alan E. RUBIN Hisayoshi YURIMOTO 《Meteoritics & planetary science》2004,39(9):1591-1598
Abstract— Several recent studies have shown that materials such as magnetite that formed in asteroids tend to have higher Δ17O (=δ17O ? 0.52 × δ18O) values than those recorded in unaltered chondrules. Other recent studies have shown that, in sets of chondrules from carbonaceous chondrites, Δ17O tends to increase as the FeO contents of the silicates increase. We report a comparison of the O isotopic composition of olivine phenocrysts in low‐FeO (≤Fa1) type I and high‐FeO (≥Fa15) type II porphyritic chondrules in the highly primitive CO3.0 chondrite Yamato‐81020. In agreement with a similar study of chondrules in CO3.0 ALH A77307 by Jones et al. (2000), Δ17O tends to increase with increasing FeO. We find that Δ17O values are resolved (but only marginally) between the two sets of olivine phenocrysts. In two of the high‐FeO chondrules, the difference between Δ17O of the late‐formed, high‐FeO phenocryst olivine and those in the low‐FeO cores of relict grains is well‐resolved (although one of the relicts is interpreted to be a partly melted amoeboid olivine inclusion by Yurimoto and Wasson [2002]). It appears that, during much of the chondrule‐forming period, there was a small upward drift in the Δ17O of nebular solids and that relict cores preserve the record of a different (and earlier) nebular environment. 相似文献
58.
Abstract Peridotite xenoliths from the subarc mantle, which have been rarely documented, are described from Iraya volcano of the Luzon arc, the Philippines, and are discussed in the context of wedge-mantle processes. They are mainly harzburgite, with subordinate dunite, and show various textures from weakly porphyroclastic (C-type) to extremely fine-grained equigranular (F-type). Textural characteristics indicate a transition from the former to the latter by recrystallization. The F-type peridotite has inclusion-rich fine-grained olivine and radially aggregated orthopyroxene, being quite different in texture from ordinary mantle-derived peridotites previously documented. Despite their strong textural contrast, the two types do not show any systematic difference in modal composition. The harzburgite of C-type has ordinary mantle peridotite mineralogy; olivine is mostly Fo91–92 and chromian spinel mostly has Cr#s (= Cr/[Cr + Al] atomic ratios) from 0.3 to 0.6. Olivine is slightly more Fe-rich (Fo89–91) and spinel is more enriched in Cr (the Cr#, 0.4–0.8) and Fe3+ in F-type peridotites than in C-type harzburgite. Orthopyroxene in F-type peridotites is relatively low in CaO (<1 wt%), Al2 O3 (<2 wt%) and Cr2 O3 (<0.4 wt%). The F-type peridotite was possibly formed from the C-type one by recrystallization including local dissolution and precipitation of orthopyroxene assisted by fluid (or melt) of subduction origin. Textural characteristics, however, indicate a deserpentinization origin from abyssal serpentinite of which protolith was a C-type peridotite. In this scenario the initial abyssal serpentinite was possibly dehydrated due to an initiation of magmatic activity beneath an incipient oceanic arc like Batan Island. The F-type peridotite is characteristic of the upper mantle of island arc, especially of incipient arc. 相似文献
59.
Masayuki Uesugi Ryo Noguchi Tooru Matsumoto Junya Matsuno Takashi Nagano Akira Tsuchiyama Shigenori Harada Kaori Yokoyama Yoshiaki Yodo Noboru Takeda Toru Yada Shogo Yakame Yuzuru Karouji Yukihiro Ishibashi Masanao Abe Tatsuaki Okada Akio Fujimura Mitsuru Ebihara Fumio Kitajima Keisuke Nagao Tomoki Nakamura Hiroshi Naraoka Takaaki Noguchi Ryuji Okazaki Hisayoshi Yurimoto 《Meteoritics & planetary science》2014,49(7):1186-1201
We report the investigation of cutting methods for Hayabusa samples. The purpose of our study is to explore the possibility of applying multiple analyses to a single particle effectively. We investigated the cutting performance of a blade dicing saw, laser, focused ion beam (FIB), and physical breaking by microindenter. Cutting performance was examined by estimating the aspect ratio of the cut slit, i.e., depth over width of the slit. We also investigated the possible contamination and sample damage by cutting. The result of the investigation shows that we can cut the samples from <50 μm to 500 μm using those methods with aspect ratios from 10 to 20, although they would introduce some contamination or damage to the samples. Our investigations also provide an important basis for the analysis of samples obtained by future sample return missions. 相似文献
60.
Ai‐Cheng Zhang Shoichi Itoh Hisayoshi Yurimoto Wei‐Biao Hsu Ru‐Cheng Wang Lawrence A. Taylor 《Meteoritics & planetary science》2016,51(1):56-69
CM chondrites are a group of primitive meteorites that have recorded the alteration history of the early solar system. We report the occurrence, chemistry, and oxygen isotopic compositions of P‐O‐rich sulfide phase in two CM chondrites (Grove Mountains [GRV] 021536 and Murchison). This P‐O‐rich sulfide is a polycrystalline aggregate of nanometer‐size grains. It occurs as isolated particles or aggregates in both CM chondrites. These grains, in the matrix and in type‐I chondrules from Murchison, were partially altered into tochilinite; however, grains enclosed by Ca‐carbonate are much less altered. This P‐O‐rich sulfide in Murchison is closely associated with magnetite, FeNi phosphide, brezinaite (Cr3S4), and eskolaite (Cr2O3). In addition to sulfur as the major component, this sulfide contains ~6.3 wt% O, ~5.4 wt% P, and minor amounts of hydrogen. Analyses of oxygen isotopes by SIMS resulted in an average δ18O value of ?22.5 ‰ and an average Δ17O value of 0.2 ± 9.2 ‰ (2σ). Limited variations in both chemical compositions and electron‐diffraction patterns imply that the P‐O‐rich sulfide may be a single phase rather than a polyphase mixture. Several features indicate that this P‐O‐rich sulfide phase formed at low temperature on the parent body, most likely through the alteration of FeNi metal (a) close association with other low‐temperature alteration products, (b) the presence of hydrogen, (c) high Δ17O values and the presence in altered mesostasis of type‐I chondrules and absence in type‐II chondrules. The textural relations of the P‐O‐rich sulfide and other low‐temperature minerals reveal at least three episodic‐alteration events on the parent body of CM chondrites (1) formation of P‐O‐rich sulfide during sulfur‐rich aqueous alteration of P‐rich FeNi metal, (2) formation of Ca‐carbonate during local carbonation, and (3) alteration of P‐O‐rich sulfide and formation of tochilinite during a period of late‐stage intensive aqueous alteration. 相似文献