Partial melting kinetics of plagioclase-diopside pairs     

Akira Tsuchiyama 《Contributions to Mineralogy and Petrology》1985,91(1):12-23

Partial melting experiments on plagioclase (An₆₀) and diopside have been carried out using pairs of large crystals to investigate textures and kinetics of melting. The experiments were done at one atmosphere pressure as a function of temperature (1,190–1,307° C) and time (1.5–192 h). Melting took place mainly at the plagioclase-diopside contact planes. Reaction zones composed of fine mixtures of calcic plagioclase and melt were developed from the surface of the plagioclase crystal inward. There exists a critical temperature, below which only a few % melting can occur over the duration of the experiments. This sluggish melting is caused by slow NaSi-CaAl diffusion in plagioclase, because the plagioclase crystal must change its composition to produce albite-rich cotectic melts. Diffusion in the solid also affects the chemical composition of the melts. During initial melting, potassium is preferentially extracted from plagioclase because K-Na diffusion in plagioclase is faster than that of NaSi-CaAl. This also causes a shift in the cotectic compositions. Above the critical temperature, on the other hand, melting is promoted by a metastable reaction in which the plagioclase composition does not change, and which produces melts with compositional gradients along the original An₆₀-diopside tie line. The critical temperature is determined by the intersection of the cotectic and the An₆₀-diopside tie line. Interdiffusion coefficients of plagioclase-diopside components in the melt are estimated from melting rates above the critical temperature by using a simplified steady-state diffusion model (e.g., 10^–8 cm²/sec at 1,300° C).Many examples of reaction zones due to partial melting have been described as spongy or fingerprint-like textures in xenoliths. Metastable melting above the critical temperature is considered to take place in natural melting where there is a high degree of melting. However, we cannot exclude the possibility of disequilibrium created by sluggish melting controlled by diffusion in the minerals. If melting occurs close to the solidus, this process can be important even for partial melting in the upper mantle.  相似文献   

Dissolution kinetics of plagioclase in the melt of the system diopside-albite-anorthite,and origin of dusty plagioclase in andesites   总被引：9，自引：5，他引：9  

Akira Tsuchiyama 《Contributions to Mineralogy and Petrology》1985,89(1):1-16

The textures and kinetics of reaction between plagioclase and melts have been investigated experimentally, and origin of dusty plagioclase in andesites has been discussed. In the experiments plagioclase of different compositions (An₉₆, An₆₁, An₅₄, An₂₃, and An₂₂) surrounded by glasses of six different compositions in the system diopside-albite-anorthite was heated at temperatures ranging from 1,200 to 1,410° C for 30 min to 88 h. Textures were closely related to temperature and chemical compositions. A crystal became smaller and rounded above the plagioclase liquidus temperature of the starting melt (glass) and remained its original euhedral shape below the liquidus. Whatever the temperature, the crystal-melt interface became rough and often more complicated (sieve-like texture composed of plagioclase-melt mixture in the scale of a few m was developed from the surface of the crystal inward; formation of mantled plagioclase) if the crystal is less calcic than the plagioclase in equilibrium with the surrounding melt, and the interface remained smooth if the crystal is more calcic than the equilibrium plagioclase. From these results the following two types of dissolution have been recognized; (1) a crystal simply dissolves in the melt which is undersaturated with respect to the phase (simple dissolution), and a crystal is partially dissolved to form mantled plagioclase by reaction between sodic plagioclase and calcic melt (partial dissolution). The amount of a crystal dissolved and reacted increased proportional to the square root of time. This suggests that these processes are controlled by diffusion, probably in the crystal.Mantled plagioclase produced in the experiments were very similar both texturally and chemically to some of the so-called resorbed plagioclase in igneous rocks. Chemical compositions and textures of plagioclase phenocrysts in island-arc andesites of magma mixing origin have been examined. Cores of clear and dusty plagioclase were clacic (about An₉₀) and sodic (about An₅₀), respectively. This result indicates that dusty plagioclases were formed by the partial melting due to reaction between sodic plagioclase already precipitated in a dacitic magma and a melt of intermediate composition in a mixed magma during the magma mixing.  相似文献   

Sulfur isotope study of Quaternary volcanic rocks from the Japanese Islands Arc     

Akira Ueda  Hitoshi Sakai 《Geochimica et cosmochimica acta》1984,48(9):1837-1848

The sulfide and sulfate contents and their δ³⁴S values were determined in Quaternary volcanic rocks from the Japanese Islands Arc. The total sulfur contents are much lower (less than 40 ppm) and the δ³⁴S values are higher (+4.4 ± 2.1) than those of ocean-floor basalts (800 ± 100 ppm and +0.8 ± 0.5, respectively; Moore and Fabbi, 1971; Sakaiet al., 1982). Lateral variations of both sulfur content and δ³⁴S values were observed in the four volcanic belts in Japan. In the Northeast Japan belt, the sulfur content (30 ± 10 ppm) of the rocks in the inner zone (the Japan Sea side) is 3 to 5 times that in the outer zone (the Pacific side), although the δ³⁴S values of the two zones are almost the same (+4.3 ± 1.0). The δ³⁴S values for the two belts in West Japan are on the average 2%. higher than those of East Japan.This study suggests that the primary magmas that formed the island arc volcanic rocks are initially depleted in sulfur (<120 ppm) and enriched in ³⁴S ($\text{δ}{}^{34}\text{S: +5 ～ +7}$) compared to ocean-floor tholeiitic basalts which formed at mantle under oceanic region. This indicates that the upper-mantle is heterogeneous in sulfur content and isotope composition.  相似文献   

The ionic conductivity in high-pressure polymorphs of calcite     

M. Ishikawa  A. Sawaoka  M. Ichikuni 《Physics and Chemistry of Minerals》1982,8(6):247-250

Ionic conductivity of polycrystalline calcite containing varying amounts of PO ₄ ^3? ions was measured in the pressure range of 1–6 GPa and at room temperature. Electrical conductivity increased with pressure corresponding to the phase transition of calcite I to calcite II. The conductivity in calcite III decreased exponentially with pressure. Calculated activation volumes of the conductivity varied with PO ₄ ^3? content in the range of 0.94–5.34 cm³/mol. This variation corresponded to the lattice parameter change of calcite I due to PO ₄ ^3? incorporation and indicated the contribution of CO ₃ ^2? -vacancies associated with PO ₄ ^3? ions to the conductivity.  相似文献   

Sea navigation, challenges and potentials in South East Asia: an assessment of suitable sites for a shipping canal in the South Thai Isthmus     

Rajesh B. Thapa  Michiro Kusanagi  Akira Kitazumi  Yuji Murayama 《GeoJournal》2007,70(2-3):161-172

This paper discusses the situation of sea navigation in south East Asia focusing on the Strait of Malacca. The strait links the Indian and Pacific oceans, which is considered one of the busiest in several narrow channels around the world. The paper highlights the significance of the strait to global maritime trade, volume of traffic, and rising environmental and social consequences in the strait. A feasibility study of constructing a new shipping canal in the South Thai Kra Isthmus as an alternative option of Malacca route had been studied since 19th century. The paper explores suitable sites for a potential shipping canal in the Kra Isthmus using physiographic spatial data i.e., elevation, sea charts, geology, soils and river systems. Each spatial data was considered as a separate decision variable for site evaluation. Separate evaluation criterions were prepared for each variable based on shipping canal requirements. Overlaying the maps in GIS environment, the variables were carefully evaluated, and five geographic sites for the canal were derived. The length of the shipping canal over sea and land was computed for each site. Site B located in south of Ranong and Chumphon provinces, was the shortest one, whereas site C in Surat Thani, Pangnna and Krabi provinces was the longest. However, each site consisted of benefits and constraints.  相似文献   

Garnet metagabbro-ultramafic complexes in the Pekulney Range, northeast Russia     

Akira  Ishiwatari  Galina V.  Ledneva  Boris A.  Bazylev  Yasutaka  Hayasaka  Suren A.  Palandzhyan  Odin L.  Morozov  Kazuto  Koizumi  Vasily D.  Stcherbakov  Sergey D.  Sokolov 《Island Arc》2007,16(1):1-3

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Dual publication     

Simon Wallis  Akira IshiwatariEditors-in-Chief  Keiji Takeuchi  Toshiaki TsunogaeExecutive Editors 《Island Arc》2007,16(2):211-211

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Carbonate deposits on submerged seamounts in the northwestern Pacific Ocean     

Hideko  Takayanagi  Yasufumi  Iryu  Tsutomu  Yamada  Motoyoshi  Oda  Kazuyuki  Yamamoto  Tokiyuki  Sato  Shun  Chiyonobu  Akira  Nishimura  Tsutomu  Nakazawa  Satoshi  Shiokawa 《Island Arc》2007,16(3):394-419

Abstract   The lithology of shallow-water carbonates collected from 19 sites on 16 seamounts in six areas of the northwestern Pacific Ocean using the Deep-sea Boring Machine System are described. The areas include the Amami Plateau, Daito Ridge, Oki-Daito Ridge, Urdaneta Plateau, Kyushu-Palau Ridge and Ogasawara Plateau. Chronological constraint is provided by calcareous nannofossil biostratigraphy, planktonic foraminiferal biostratigraphy, larger foraminiferal biostratigraphy and strontium (Sr) isotope stratigraphy. Large amounts of shallow-water carbonates accumulated on the seamounts during the Oligocene, a relatively cool period, whereas limited carbonate deposits formed during the Early Miocene, a relatively warm period. This might indicate that deposition of shallow-water carbonates on seamounts in the northwestern Pacific Ocean was not necessarily controlled by climatic conditions, but was related to volcanism and tectonics that served as foundations for reef/carbonate-platform formation. Remarkable differences in biotic composition exist between Cretaceous and Cenozoic shallow-water carbonates. Late Cretaceous shallow-water carbonates are distinguished by the occurrence of rudists, solenoporacean algae and microencrusters. Middle Eocene to Early Oligocene shallow-water carbonates are dominated by Halimeda or nummulitid and discocyclinid larger foraminifers. Scleractinian corals became common from the Oligocene onward. Nongeniculate coralline algae and larger foraminifers were common to abundant throughout the Eocene to the Pleistocene. The replacement of major carbonate producers in the shallow-water carbonate factory during post-Cretaceous time is in accordance with previous studies and is considered to reflect a shift in seawater chemistry.  相似文献   

Analysis of Physical and Chemical Parameters for Discrimination of Water Origin in a Hydroelectric Reservoir     

Wagner José Barreto  Ieda Scarminio  Maria Cristina Solci  Dílson Norio Ishikawa  Melissa Tiemi Ogasawara  Sônia Naomi Nomi  Sônia Regina Giancoli Barreto 《洁净——土壤、空气、水》2007,35(3):239-245

Seventeen physical and chemical parameters were obtained from a hydroelectric reservoir located in a tropical region in the south of Brazil. Multivariate Principal Component Analysis (PCA) and Hierarchical Group Analysis (HGA) were used to identify the parameters discriminating the origin of water from the Tibagi and the Primeiro de Maio River, after it has passed the mixing region. The study was conducted during the dry and rainy seasons in July 2002 and February 2003 at three depths and three sampling sites located 0, 5, and 10 km away from the mixing region. The statistical methods showed to be appropriate for identifying the contribution of each tributary in the water mixing site of a complex water system. The most important discriminating parameter was the absorbance relation A(253 nm)/A(203 nm), followed by the concentrations of Fe(III), Mn(III), and Ni(II). An anthropogenic interference was found in the reservoir due to high Ni(II) and orthophosphate concentrations caused by a nearby town sewage discharge. The interference was more important during the dry periods due to the lower dispersion of the pollutants. Urgent initiatives should be taken from the state government to build treatment stations for the wastewater of the small cities around the Capivara hydroelectric reservoir to prevent the drinking water quality from deteriorating.  相似文献   

Magnetic petrology of the 1991–1995 dacite lava of Unzen volcano,Japan: Degree of oxidation and implications for the growth of lava domes     

Takeshi Saito  Naoto Ishikawa  Hiroki Kamata 《Journal of Volcanology and Geothermal Research》2007

To understand the oxidation state and process of oxidation of lava domes, we carried out magnetic petrological analyses of lava samples obtained from domes and block-and-ash-flow deposits associated with the 1991–1995 eruption of Unzen volcano, Japan. As a result, we recognize three different types of magnetic petrology, each related to deuteric high-temperature oxidation during initial cooling. Type A oxides are characterized by homogenous titanomagnetite and titanohematite, indicating a low oxidation state and high titanomagnetite concentrations. Type B oxides are weakly exsolved and contain titanohematite laths and rutile lenses, indicating a higher oxidation state. Type C oxides, which represent the highest oxidation state, are completely exsolved and composed of Ti-poor titanomagnetite, titanohematite, rutile, and pseudobrookite, indicating high hematite concentrations. Some grains in Types A and B show indications of reduction, which was related to interaction with volcanic gases subsequent to high-temperature oxidation. In terms of geological occurrence, the oxidation processes probably differed for endogenous and exogenous domes. Endogenous dome lavas are oxidized concentrically and are classified into the three types according to their location within the dome: samples from the surface are strongly oxidized and classified as Type C, while the inner part is unoxidized and classified as Type A. Exogenous dome lavas are unoxidized and assigned to Type A. Some samples show signs of reduction, which may have occurred around fumaroles. We propose that location within the dome and the process of dome growth are the factors that control oxidation.  相似文献