The Preparation and Preliminary Characterisation of Four New Geological Survey of Japan Geochemical Reference Materials: Soils, JSO-1 and JSO-2; and Marine Sediments, JMS-1 and JMS-2   总被引：1，自引：0，他引：1  

Shigeru Terashima  Noboru Imai  Masahiro Taniguchi  Takashi Okai  Akira Nishimura 《Geostandards and Geoanalytical Research》2002,26(1):85-94

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A Study on the Formation of Smectite in Silica Scales Precipitated from Geothermal Water: The Effect of Magnesium     

Yoshinobu Aramaki    Takushi Yokoyama  Yoshihiro Okaue  Akira Imai  Koichiro Watanabe 《Resource Geology》2005,55(3):281-284

Abstract. Silica scales containing large amounts of smectite were recently found in the pipelines for geothermal water at a geothermal power plant. To elucidate the mechanism of smectite formation, seven silica scale samples were characterized by powder X-ray diffraction, chemical analysis and ²⁷A1 MAS NMR. Smectite was present in samples with MgO levels above 10 wt% and Al₂O₃ levels below 10 wt%. In ²⁷A1 MAS NMR spectra, peaks assigned to both tetrahedrally and octahedrally coordinated aluminum (Al(4) and Al(6)) were observed for Mg-rich samples, whereas a peak due to Al(4) alone appeared in Mg-poor samples. From these observation and comparison between ²⁷A1 MAS NMR spectra for synthesized precipitates of Al₂O₃-SiO₂ containing MgO and not containing MgO, it is concluded that magnesium plays an important role in the stabilization of Al(6), and results in the formation of smectite  相似文献   

Geochronological Constraints Using ⁴⁰Ar/³⁹Ar Dating on the Mineralization of the Hishikari Epithermal Gold Deposit, Japan     

Kenzo Sanematsu    Robert Duncan  Akira Imai  Koichiro Watanabe 《Resource Geology》2005,55(3):249-266

Abstract. Ages for thirty adularia samples collected from various veins were in the Hishikari gold deposit determined by ⁴⁰Ar/³⁹Ar dating to constrain the timing of adularia‐quartz vein formation and to determine the temporal change in temperature of hydrothermal fluid. Plateau ages were obtained from all adularia samples, and significant excess ⁴⁰Ar is not recognized from inverse isochrones. The duration of mineralization within individual veins was determined by adularia ages from the early and late stages of mineralization within the same vein. The durations of mineralization in the Daisen‐1, Daisen‐3, Hosen‐2 and Keisen‐3 veins in the Honko‐Sanjin zone were 7,000, 140,000, 160,000 and 170,000 years, respectively. The durations of mineralization in the Seisen‐2 and Yusen‐1–2 veins in the Yamada zones were 360,000 and 320,000 years, respectively. Mineralization lasted for a relatively longer period in individual veins at the Yamada zone. Mineralization ages from the Honko‐Sanjin zone range from 1.04 to 0.75 Ma, and most mineralization ages are concentrated in a short period from 1.01 to 0.88 Ma. In contrast, mineralization ages for the Yamada zone range from 1.21 to 0.64 Ma. These results indicate that fracturing and subsequent vein formation lasted for a longer period in the Yamada zone (about 570,000 years) compared with those events in the Honko‐Sanjin zone (about 290,000 years). The homogenization temperatures of liquid‐rich fluid inclusions in columnar adularia used for age determination were determined to be 223°C on average, and most of these temperatures range from 180 to 258d?C. No significant temporal change in homogenization temperature is recognized in this study. However, adularia in the Keisen veins indicated higher homogenization temperatures compared with elsewhere in the deposit, suggesting that the principal ascent of mineralizing hydrothermal fluid was via the Keisen veins.  相似文献   

Compressibility of the calcium aluminosilicate, CAS, phase to 44 GPa     

Shigeaki Ono  Tsuyoshi Iizuka  Takumi Kikegawa 《Physics of the Earth and Planetary Interiors》2005,150(4):331-338

In situ X-ray diffraction measurements on a calcium aluminosilicate (CAS) phase have been carried out using a laser-heated diamond anvil cell up to a pressure of 44 GPa, employing a synchrotron radiation source. CAS is the major mineral formed from sediments subducted into the Earth's mantle. The sample was heated using a YAG laser after each pressure increment to relax the deviatoric stress in the sample. X-ray diffraction measurements were carried out at T = 300 K using an angle-dispersive technique. The pressure was calculated using an internal platinum metal pressure calibrant. The Birch–Murnaghan equation of state for the CAS phase obtained from the experimental unit cell parameters showed a density of ρ₀ = 3.888 g/cm³ and a bulk modulus of K₀ = 229 ± 9 GPa for K^′₀ = 4.7 ± 0.7. When the first pressure derivative of the bulk modulus was fixed at K^′₀ = 4, then the value of K₀ = 239 ± 2 GPa. From the experimental compressibility, the density of the CAS phase was observed to be lower than the density of co-existing Al-bearing stishovite, calcium perovskite, calcium ferrite-type phases, and (Fe,Al)-bearing Mg-perovskite in subducted sediments in the lower mantle. Therefore, the density of subducted sediments in the lower mantle decreases with increasing mineral proportion of the CAS phase.  相似文献   

Resource depletion calculated by the ratio of the reserve plus cumulative consumption to the crustal abundance for gold   总被引：1，自引：0，他引：1  

Takashi Nishiyama  Tsuyoshi Adachi 《Natural Resources Research》1995,4(3):253-261

The magnitude of the world's mineral consumption has increased sharply, and there is no sign that growth is likely to stop in the near future. Currently, new discoveries and technology add to the reserves of varous mineral commodities at a rate that has exceeded depletion. As a result, life expectancies have remained nearly constant. However, it is questionable whether this condition is sustainable in the future. Therefore, most of our attention to the future has been focused on potentially recoverable resources. The potentially recoverable resources for 35 minerals in the Earth's crust were estimated based on the relationship between crustal abundance and the reserve of currently recoverable gold. The ratio of the reserve plus cumulative consumption to the abundance of gold is appropriate for calculating reserves of other mineral resources because gold has the highest profit margin for exploration of reserves. From an economic perspective, the price of gold is 350 times the mean value of 33 other resources for calculating production versus price. New mining technologies and new processing methods have been developed during the last 20 years as a response to high prices. As a result, five times the reserves available in 1970 have now been discovered, and two times the reserves available in 1970 were consumed during the past two decades. It is questionable whether other mineral commodities can reach the ratio of reserve plus cumulative consumption to abundance that gold does. Using this concept, the limit of the Earth's resources under present technology was calculated for 35 mineral resources, based on the ratio of the reserve plus cumulative consumption to abundance for gold. Even though recoverable tonnage of lead, silver, tin, boron, copper, and mercury from ore deposits in the Earth's crust is relatively low, the abundance of these metals is apparently sufficient for future supplies. However, considering the special situation of gold created by its very high price compared to world production, there is anxiety concerning steep increases in the price or depletion of these metals, which have a shorter lifetime from a geochemical point of view.  相似文献   

Characteristics of the Cibaliung Gold Deposit: Miocene Low-Sulfidation-Type Epithermal Gold Deposit in Western Java, Indonesia     

Agung Harijoko    Yukiko Ohbuchi    Yoshinobu Motomura    Akira Imai  Koichiro Watanabe 《Resource Geology》2007,57(2):114-123

Middle Miocene (11.18–10.65 Ma) low sulfidation‐type epithermal gold mineralization occurred in the Cibaliung area, southwestern part of Java Island, Indonesia. It is hosted by andesitic to basaltic andesitic lavas of the Middle Miocene Honje Formation (11.4 Ma) and is covered by Pliocene Cibaliung tuff (4.9 Ma). The exploration estimates mineral resource of approximately 1.3 million tonnes at 10.42 g/t gold and 60.7 g/t silver at a 3 g/t Au cut‐off. This equates to approximately 435,000 ounces of gold and 2.54 million ounces of silver. That resource resulted from two ore shoots: Cibitung and Cikoneng. Studies on ore mineralogy, hydrothermal alteration, geology, fluid inclusion, stable isotopes and age dating were conducted in order to characterize the deposit and to understand a possible mechanism of preservation of the deposit. The ore mineral assemblage of the deposit consists of electrum, naumannite, Ag‐Se‐Te sulfide minerals, chalcopyrite, pyrite, sphalerite and galena. Those ore minerals occur in quartz veins showing colloform–crustiform texture. They are enveloped by mixed layer clay illite/smectite zone, which grades into smectite zone outward. The temperature of mineralization revealed by fluid inclusion study on quartz in the veins ranges from 170 and 220°C at shallow and deep level, respectively. The temperature range is in agreement with the temperature deduced from the hydrothermal alteration mineral assemblage including mixed layered illite/smectite and laumontite. The mineralizing fluid is dilute, with a salinity <1 wt% NaCl equivalent and has stable isotopes of oxygen and hydrogen composition indicating a meteoric water origin. Although the deposit is old enough that it would have been eroded in a tropical island arc setting, the coverage by younger volcanic deposits such as the Citeluk tuff and the Cibaliung tuff most probably prevented this erosion.  相似文献   

Occurrences of Ore Minerals and Fluid Inclusion Study on the Kingking Porphyry Copper–Gold Deposit, Eastern Mindanao, Philippines     

Leilanie O. Suerte    Sho Nishihara    Akira Imai    Koichiro Watanabe    Graciano P. Yumul  Jr Victor B. Maglambayan 《Resource Geology》2007,57(2):219-229

The Kingking deposit is a gold‐rich porphyry copper deposit and the southernmost deposit at the eastern Mindanao mineralized belt, Philippines. It is underlain by Cretaceous–Paleogene sedimentary and volcanic rocks that are intruded by mineralized Miocene diorite porphyries and by barren Miocene–Pliocene dacite and diorite porphyries. The main alteration zones in the deposit are the inner potassic zone and the outer propylitic zone. The biotite‐bearing diorite and hornblende diorite porphyries are the primary host rocks of mineralization. Two dominant copper minerals, bornite and chalcopyrite, which usually occur as fracture fillings, are associated with fine crystalline quartz veinlet stockworks in the mineralized diorites. Minor secondary covellite, chalcocite and digenite are also observed. The primary Cu‐Fe sulfide phases initially deposited from ore fluids consisted of bornite solid solution (bnss) and intermediate solid solution (iss), which decomposed to form the bornite and chalcopyrite. Peculiar bornite pods that are different from dissemination and are associated with volcanic rock xenoliths in biotite‐bearing diorite porphyry are noted in a drill hole. These pods of bornite are not associated with quartz veinlet stockworks. Fluid inclusion analyses show three types of inclusions contained in Kingking samples: two‐phase fluid‐rich and vapor‐rich inclusions and polyphase hypersaline inclusions from porphyry‐type quartz veinlet stockworks. The liquid–vapor homogenization temperatures (T_H) and the dissolution temperature of halite daughter crystals (T_M) from the polyphase hypersaline inclusions predominantly range from 400°C up to >500°C. The wide range of T_H and T_M may be due to heterogeneous trapping of variable ratios of vapor and brine. For some inclusions, T_H > T_M and in some cases, T_H < T_M, indicating that some of the brine was supersaturated or saturated with NaCl at the time of entrapment. Calculated salinity of the polyphase hypersaline inclusions ranges from 40 to 60% NaCl equivalent. Temperature and vapor pressure of mineralized fluid were estimated to be 400°C and 16 MPa.  相似文献   

Porphyry-Type Mineralization at Selogiri Area, Wonogiri Regency, Central Java, Indonesia     

Akira Imai    Jumpei Shinomiya    Maung Thiha Soe    Lucas Donny Setijadji    Koichiro Watanabe  I Wayan Warmada 《Resource Geology》2007,57(2):230-240

The Selogiri area, situated in Wonogiri regency, Central Java, is one of several gold prospecting areas in the Southern areas Mountain Range in Java, Indonesia. Three types of dioritic–andesitic intrusive rocks occur in the Selogiri area, namely, hornblende andesite porphyry, hornblende diorite porphyry and hornblende diorite, exposed in a half‐circular depression where volcanic breccia and tuff are widely distributed. The occurrence of stockwork quartz veinlets and associated with magnetite and malachite coating along the cracks in the diorite porphyry suggests porphyry type mineralization. This is also supported by the occurrence of polyphase hypersaline fluid inclusions in the stockwork veinlet quartz. Small‐scale miners are mining NS‐trending quartz veins for gold associated with base metal sulfides. These veins are probably epithermal‐type mineralization that overprinted porphyry‐type mineralization. The Neogene intermediate to silicic hydrous magmatism in Java could have formed the porphyry‐type mineralization in Selogiri, as in the rest of the Sunda–Banda arc.  相似文献   

Elemental distribution of coastal sea and stream sediments in the island-arc region of Japan and mass transfer processes from terrestrial to marine environments     

Atsuyuki Ohta  Noboru Imai  Shigeru Terashima  Yoshiko Tachibana  Ken Ikehara  Takashi Okai  Masumi Ujiie-Mikoshiba  Ran Kubota 《Applied Geochemistry》2007,22(12):2872

A total of 49 elements have been identified in 338 coastal sea sediment samples collected from an area situated off the Ise-Tokai region of Japan for a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define the natural geochemical background variation, mass transport, and contamination processes. The elemental concentrations of coastal sea sediments are determined primarily by particle size and regional differences. Most elemental concentrations increase with a decrease in particle size. Some elements such as Ca, Mn, and Yb are found to exist in large quantities in coarse particles containing calcareous shells, Fe–Mn oxides, and felsic volcanic sediments. Regional differences reflect the mass transfer process from terrestrial areas to coastal seas and the influence of the local marine geology. An analysis of variance (ANOVA) reveals that for many elements, the particle size effect is predominant over regional difference. The mean chemical compositions of coastal sea sediments are similar to those of stream sediments in adjacent terrestrial areas and in the upper crust of Japan. This observation supports the fact that coastal sea sediments have certainly originated from terrestrial materials. However, the spatial distributions of elemental concentrations are not always continuous between the land and coastal seas. The scale of mass movement observed in marine geochemical maps occurs at a distance of 20 km from the river mouth. A detailed examination of the spatial distribution patterns of K (K₂O) and Cr concentrations suggests that terrestrial materials supplied through rivers are deposited near the shore initially, and then gravity-driven processes shift the sediments deeper into the basin. Contamination with heavy metals such as Zn, Cd and Pb was observed in coastal bays surrounded by urban and industrial areas. It is noteworthy that the areas with the highest concentration of these elements usually do not occur near the shore (not near the contamination source) but at the center of the bay. Unexpected low concentrations of Zn, Cd and Pb near shore may either be due to a decreased anthropogenic load in the most recent sediments or to dilution by unpolluted flood sediments.  相似文献   

Os, Nd, and Sr isotopic and chemical compositions of ultramafic xenoliths from Kurose, SW Japan: Implications for contribution of slab-derived material to wedge mantle     

Ryoko Senda  Tsuyoshi Tanaka  Katsuhiko Suzuki 《Lithos》2007,95(3-4):229-242

We examined seven ultramafic xenoliths from 1~3 Ma alkali olivine basalt reefs near the Eurasian continent and one sample of the host alkali basalt to identify the mantle wedge material and to constrain the origin and evolution of mantle beneath SW Japan. Six xenoliths are from Kurose and one xenolith is from Takashima, northern part of the Kyushu islands, SW Japan. The Sr and Nd isotopic ratios vary from 0.70416 to 0.70773 and from 0.51228 to 0.51283, respectively. The Kurose and Takashima xenoliths have higher Sr isotopic ratios and lower Nd isotopic ratios than those of the peridotite xenoliths from the other arc settings such as Simcoe and NE Japan.

The Kurose xenoliths have less radiogenic Os isotopic ratios (¹⁸⁷Os/¹⁸⁸Os = 0.123–0.129) than the primitive upper mantle (PUM) estimate and limited variation compared to the other arc xenoliths. Their Os isotope compositions are rather similar to the ultramafic xenoliths from NE and east China. In addition, the samples of the Kurose and Takashima xenoliths plot along a mixing line between ultramafic xenoliths from SE and NE China and a slab component in Sr–Nd–Os isotopic space. Our results suggest that fragments of continental lithospheric mantle from the China craton may exist beneath Kurose and Takashima after the Sea of Japan expansion when the Japanese islands were rifted away from the Eurasian continent during Miocene. Later magmatism due to subduction of the Philippine Sea Plate beneath the SW Japan arc around 15 Ma ago may have introduced fluids or melts derived from slab component, interpreted to be oceanic sediments rather than altered oceanic crust, that possibly modified the original composition of the lithospheric mantle sampled by the peridotite xenoliths from Kurose and Takashima.  相似文献