Examination of mineral assemblage and chemical composition in the fracture zone of the Nojima Fault at a depth of 1140 m: Analyses of the Hirabayashi NIED drill cores     

Tatsuo Matsuda  Takashi Arai  Ryuji Ikeda  Kentaro Omura  Kenta Kobayashi  Hiroyuki Sano  Takashi Sawaguchi  Hidemi Tanaka  Tomoaki Tomita  Naoto Tomida  Satoshi Hirano  Akiko Ymazaki 《Island Arc》2001,10(3-4):422-429

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The mesozoic evolution of the mino terrane, central Japan: A geologic and paleomagnetic synthesis   总被引：1，自引：0，他引：1  

Isamu Hattori 《Tectonophysics》1982,85(3-4)

The Mino tectono-stratigraphic terrane, central Japan, underlain by Permian to Jurassic sedimentary and volcanic rocks of various origins, was formed through accretion processes associated with the Mesozoic sea-floor spreading. This conclusion has been reached mainly from the following reasoning:

1. (1) the entire boundary of this terrane is defined by tectonic belts with high-pressure metamorphic rocks and serpentinized ultramafic rocks,

2. (2) the chemistry and petrology of the Permian greenstones demonstrate their affinity with abyssal tholeiitic and alkalic basalts,

3. (3) the widespread, but chaotic, occurrence of Permian greenstones, Triassic cherts, and Jurassic siliceous shales in the younger Jurassic clastic rocks of this terrane suggests extensive post-depositional mixing of strata,

4. (4) the sedimentology of the Jurassic sandstones strongly suggests that they are turbidity-current deposits supplied from cratonic lands,

5. (5) the South-Pacific type fossil assemblage in the Mino terrane shows strong contrast with the North-Pacific type fossil assemblage of the adjacent terranes,

6. (6) the paleomagnetism of the Permian and Jurassic greenstones, the Triassic cherts, and the Jurassic siliceous shales implies long-distance northward drift in Cretaceous time of these rocks from their original low latitudinal regions.

Along with this northward migration, the Mino terrane was accreted with extensive internal deformation to northeast Asia including the present Hida terrane. Recent accumulation of paleomagnetic and paleontologic data in the Pacific peripheral regions appears to support the existence of many allochthonous terranes which migrated from the equatorial regions. The Mino terane may be regarded as one example of these Circum-Pacific allochthons.  相似文献   

Stochastic analysis of bed-thickness distribution of sediments     

S. Mizutani  I. Hattori 《Mathematical Geosciences》1972,4(2):123-146

On formation of a bed and distribution of bed thickness, A. N. Kolmogorov presented a mathematical explanation that if repetitive alternations of material accumulation and erosion form a sequence of beds, the resultant bed-thickness distribution curve takes a shape truncated by the ordinate at zero thickness. In this truncated distribution curve, its continuation and extension from positive to negative thickness represents the distribution of beds with negative thickness, that is, the depth of erosion. When a distribution curve, including both positive and negative parts, is expressed by a function f(x),the ratio \(\int_0^\infty {f(x)dx to} \int_{ - \infty }^\infty {f(x)dx} \) ,called Kolmogorov's coefficient and designated as p,is a parameter representing the degree of accumulation in the depositional environment. On the assumption that f(x)is described by the Gaussian distribution function, the coefficient pfor Permian and Pliocene sequences in central Japan was calculated. The coefficients also were obtained from published data for different types of sediments from other areas. It was determined that they are more or less different depending on their depositional environments. The calculated results are summarized as follows: $$\begin{gathered} p = 0.80 - 1.0for{\text{ }}alluvial{\text{ }}or{\text{ }}fluvial{\text{ }}deposits \hfill \\ p = 0.65 - 0.95for{\text{ }}nearshore{\text{ }}sediments \hfill \\ p = 0.55 - 0.95for{\text{ }}geosynclinal{\text{ }}sediments \hfill \\ p = 0.90 - 1.0for{\text{ }}varves \hfill \\ \end{gathered} $$ In addition, a ratio \(q = \int_0^\infty {xf(x)dx/} \int_{ - \infty }^\infty {|x|f(x)dx} \) ,called Kolmogorov's ratio in this paper, is introduced for estimating a degree of total thickness actually observed in the field relative to total thickness once present in a basin. The calculated results of Kolmogorov's ratio are as follows: $$\begin{gathered} q = 0.88 - 1.0for{\text{ }}alluvial{\text{ }}or{\text{ }}fluvial{\text{ }}deposits \hfill \\ q = 0.68 - 0.98for{\text{ }}nearshore{\text{ }}sediments \hfill \\ q = 0.55 - 0.96for{\text{ }}geosynclinal{\text{ }}sediments \hfill \\ q = 0.92 - 1.0for{\text{ }}varves \hfill \\ \end{gathered} $$ The sedimentological significance of these values is discussed.  相似文献   

Contributions from mafic alkaline magmas to the Bingham porphyry Cu–Au–Mo deposit, Utah, USA   总被引：1，自引：0，他引：1  

Daniel T. Maughan  Jeffrey D. Keith  Eric H. Christiansen  Tamalyn Pulsipher  Keiko Hattori  Noreen J. Evans 《Mineralium Deposita》2002,37(1):14-37

The Bingham porphyry Cu-Au-Mo deposit, Utah, may only be world-class because of substantial contributions of sulfur and metals from mafic alkaline magma to an otherwise unremarkable calc-alkaline system. Volcanic mafic alkaline rocks in the district are enriched in Cr, Ni, and Ba as well as Cu, Au, platinum group elements (PGE), and S. The bulk of the volcanic section that is co-magmatic with ore-related porphyries is dacitic to trachytic in composition, but has inherited the geochemical signature of high Cr, Ni, and Ba from magma mixing with the mafic alkaline rocks. The volcanic section that most closely correlates in time with ore-related porphyries is very heterogeneous containing clasts of scoriaceous latite, latitic, and minette, and flows of melanephelinite, shoshonite, and olivine latite in addition to volumetrically dominant dacite/trachyte. Bingham ore-related porphyries show ample evidence of prior mixing with mafic alkaline magmas. Intrusive porphyries that have not been previously well-studied have several chemical and mineralogical indications of magma mixing. These "mixed" lithologies include the hybrid quartz monzonite porphyry, biotite porphyry, and minette dikes. Even some of the more silicic latite and monzonite porphyries retain high Cr and Ba contents indicative of mixing and contain trace amounts of sapphire (<1 mm). The heterogeneous block and ash flow deposits also contain sapphire and are permissively correlated with the intrusions based on chemical, mineralogical, and isotopic data. Magma mixing calculations suggest about 10% of the monzonitic/latitic ore-related magma may have been derived from mafic alkaline magma similar to the melanephelinite. If the original S content of the mafic magma was about 2,000-4,000 ppm, comparable with similar magmas, then the mafic magma may have been responsible for contributing more than half of the S and a significant portion of the Cu, Au, and PGE in the Bingham deposit.  相似文献   

Carbonatization of oceanic crust by the seafloor hydrothermal activity and its significance as a CO₂ sink in the Early Archean     

Kentaro Nakamura 《Geochimica et cosmochimica acta》2004,68(22):4595-4618

Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO₂ flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO₂ fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ¹³C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K₂O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K₂O, Rb, and Ba, and are depleted in Na₂O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO₂ enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO₂ in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO₂ ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 10¹³ mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10^-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 10¹¹ cm²/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO₂ in the Early Archean.  相似文献   

Geochemical Features and Tectonic Setting of Greenstones from Kunimiyama, Northern Chichibu Belt, Central Shikoku, Japan     

Tatsuo Nozaki    Kentaro Nakamura  Hiroshi Osawa    Koichiro Fujinaga  Yasuhiro Kato 《Resource Geology》2005,55(4):301-310

Abstract. We report whole‐rock chemical data for the greenstones from the Kunimiyama area in the Northern Chichibu Belt and their implications on the tectonic setting of these rocks. The Kunimiyama greenstones are associated with stratiform fer‐romanganese deposits or bedded cherts in the northern part of the study area, but are closely associated with a thick limestone block or bedded cherts in the southern part. The constituent minerals of greenstones are albitized plagioclase, clinopy‐roxene, chlorite, calcite, epidote, pumpellyite, prehnite, quartz, celadonite, sericite and opaque minerals such as iron oxyhy‐droxide and hematite. These mineral assemblages, epidote + pumpellyite + chlorite and chlorite + pumpellyite + prehnite, suggest that the metamorphic grade of greenstones from the Kunimiyama area is prehnite‐pumpellyite facies. The whole‐rock chemical compositions of greenstones associated with ferromanganese deposits are generally similar to those of normal mid‐ocean ridge basalt (N‐MORB). In contrast, the chemical compositions of the greenstones associated with the limestone block are comparable to those of ocean island alkaline basalt. Greenstones associated with bedded cherts are of enriched MORB and ocean island basalt, as well as N‐MORB origins, suggesting they probably formed as a result of plume‐related MOR volcanism in the Panthalassa Ocean in Early Permian and by tectonic mixing of ocean island basalts with oceanic ridge crustal fragments during accretion/subduction processes. These geological and geochemical lines of evidence suggest that the Kunimiyama greenstones are allochthonous blocks of accreted oceanic crust and seamounts. The ferromanganese deposits are frequently accompanied by reddish greenstones. Compared to common greenish greenstones, the reddish greenstones are characterized by high MnO and rare earth element contents and distinct negative Ce anomalies, implying a slight contribution of hydro thermal component forming the ferromanganese deposits.  相似文献   

Contribution of mafic melt to porphyry copper mineralization: evidence from Mount Pinatubo, Philippines, and Bingham Canyon, Utah, USA   总被引：13，自引：0，他引：13  

Kéiko H. Hattori  Jeffrey D. Keith 《Mineralium Deposita》2001,36(8):799-806

Mount Pinatubo in the Philippines, known for its cataclysmic eruption in 1991, hosts several porphyry copper deposits and active geothermal systems. An underlying mafic melt supplied much of the sulphur for the dacitic magma and its injection into the dacitic magma chamber triggered the eruption. The eruption caused purging of the sulphur-rich fluid from the dacite to the atmosphere and extensive fracturing. Similar events took place at Bingham Canyon, Utah, site of the largest copper and gold deposit in North America at 38 Ma. The Bingham Canyon mineralization took place beneath an active stratovolcano and pyroclastic flows contemporaneous with the mineralization show evidence for magma mingling. Ascent of mafic melt supplied sulphur and chalcophile elements to the felsic magma, which consolidated to form the Bingham stock and its underlying magma chamber. Injections of the mafic melt caused periodic eruptions of felsic magma to form the stratovolcano and deposition of sulphide minerals in highly fractured rocks in and around the stock.  相似文献   

Pyrite of distinctive isotopic composition from the Hemlo deposit: A potential tool to identify this type of gold mineralization in Archean terrain     

Keiko Hattori  Eion M. Cameron   《Journal of Geochemical Exploration》1987,28(1-3)

Most sulphides from various rock types and mineralization of Archean age exhibit sulphur isotope values (δ³⁴S) near 0‰. This is due to a general absence of conditions suitable for the oxidation-reduction reactions essential for isotopic fractionation. However, some important occurrences of Archean Au mineralization do display significant variations in δ³⁴S). One such occurrence with unusual isotopic compositions is the Hemlo gold deposit: pyrite from the ore typically has δ³⁴S < −6‰ to a minimum value of −17.5‰ The isotopic composition of the pyrite is correlated with the content of Au, indicating that they are genetically related.The sulphur isotope data suggest that sulphur compounds experienced redox reactions in the hydrothermal system at Hemlo and that sulphate was present prior to the Au mineralization. This sulphate may be of exogenic origin from a restricted basin, or of endogenic origin from magmatic-hydrothermal fluids. Other characteristic features of the deposit, such as enrichment in Sb, Tl and Hg, may also be explained by ore deposition under moderately oxidizing conditions.Distinctive δ³⁴S values were also observed in pyrite from Au mineralization at Heron Bay, 30 km west of Hemlo, and from baritic strata 21 to 27 km west and on approximate strike from Hemlo. These occurrences also represent sulphate-bearing hydrothermal systems and, as such, give distant information on the unusual environment of the mineralization at Hemlo. Since the isotopes of sulphur are sensitive to oxidation conditions they may be used to identify hydrothermal activities characteristic of this type of Au mineralization and to explore for other unusual areas of sulphate accumulation in Archean terrains.  相似文献   

A Simple Method for Precise Determination of 23 Trace Elements in Granitic Rocks by ICP-MS after Lithium Tetraborate Fusion   总被引：1，自引：0，他引：1  

Shunsaku Awaji    Kentaro Nakamura  Tatsuo Nozaki  Yasuhiro Kato 《Resource Geology》2006,56(4):471-478

Abstract. An improved alkali fusion method followed by HF-HNO₃-HC1O₄ treatment is performed for simultaneous determination of 23 trace elements (Sr, Y, Zr, Nb, Ba, Hf, Ta, Th, U, and REE) by ICP-MS in rock reference materials: basaltic rocks (JB-2, JB-3) and granitic rocks (JG-la, JG-2, JG-3). Our improved method offers several advantages including: (1) suppression of whitish precipitates probably composed of insoluble fluorides by addition of HCIO4, (2) simple and reliable preparation procedure, (3) instrument calibration which enables straightforward simultaneous multi-elemental analysis, and (4) the very low background levels by using pure lithium tetraborate flux. We obtained the analytical results with a reproducibility of mostly <2 % (1) for the basaltic rocks and <7 % for the granitic rocks. The higher relative standard deviation (RSD) values for granitic rocks may be attributed to sample heterogeneity of coarse-grained granitic rocks. The analytical results of the granitic rocks demonstrate that Zr and Hf abundances are consistent with the compiled values and that REE concentrations agree well with recently published data, suggesting that the Li₂B₄O₇ fusion method applied in the present study is suitable for the analysis of the granitic rocks.  相似文献   

Whole-rock Geochemistry of Basic Schists from the Besshi Area, Central Shikoku: Implications for the Tectonic Setting of the Besshi Sulfide Deposit     

Tatsuo Nozaki    Kentaro Nakamura  Shunsaku Awaji  Yasuhiro Kato 《Resource Geology》2006,56(4):423-432

Abstract. Whole-rock chemical compositions of the Besshi basic schist closely associated with the Besshi massive sulfide deposit from the Sanbagawa Belt are reported. Studied samples were collected from four outcrops around the Dozan-goe, central Shikoku. Common metamorphic mineral assemblage of the basic schist is albite + epidote + actinolite + chlorite ± muscovite ± quartz. Major element contents are similar to those of typical tholeiitic basalts. Trace element patterns of the basic schist normalized to normal mid-ocean ridge basalt (N-MORB) are generally flat, although concentrations of highly mobile large-ion lithophile elements are quite variable. Chondrite-normalized rare earth element (REE) patterns are flat to slightly light REE-depleted patterns. In the Hf-Th-Ta and Nb-Zr-Y discrimination diagrams, basic schist samples closely associated with the sulfide deposit are plotted within the N-MORB field. The Th/Nb ratios of the basic schist are also comparable to those of N-MORB. These geo-chemical lines of evidence indicate that the protolith of the Besshi basic schist is N-MORB and the Besshi sulfide deposit was formed by hydrothermal activity in conjunction with MOR volcanism.  相似文献