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21.
Ram C. Sharma Ryutaro Tateishi Keitarou Hara Saeid Gharechelou Kotaro Iizuka 《International Journal of Digital Earth》2016,9(10):1004-1020
An improved methodology for the extraction and mapping of urban built-up areas at a global scale is presented in this study. The Moderate Resolution Imaging Spectroradiometer (MODIS)-based multispectral data were combined with the Visible Infrared Imager Radiometer Suite (VIIRS)-based nighttime light (NTL) data for robust extraction and mapping of urban built-up areas. The MODIS-based newly proposed Urban Built-up Index (UBI) was combined with NTL data, and the resulting Enhanced UBI (EUBI) was used as a single master image for global extraction of urban built-up areas. Due to higher variation of the EUBI with respect to geographical regions, a region-specific threshold approach was used to extract urban built-up areas. This research provided 500-m-resolution global urban built-up map of year 2014. The resulted map was compared with three existing moderate-resolution global maps and one high-resolution map in the United States. The comparative analysis demonstrated finer details of the urban built-up cover estimated by the resultant map. 相似文献
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The Mupane gold deposit, which is one of the numerous gold occurrences in the Tati Greenstone Belt in the northeastern part of Botswana, consists of four orebodies, namely Tau, Tawana, Kwena, and Tholo deposits. The present research, which focuses on the genesis of the Tau deposit, was based on ore petrography, mineral chemistry of sulfides, and sulfur isotope data. Mineralogical characteristics of the host rocks indicate that banded iron formation at the Tau deposit includes iron oxides (magnetite), carbonates (siderite and ankerite), silicates (chlorite and amphibole), and sulfides (arsenopyrite and pyrrhotite). The deposit features arsenopyrite-rich zones associated with biotite-chlorite veins, which are indicative of the precipitation of arsenopyrite concomitant with potassic alteration. The replacement of magnetite by pyrrhotite in some samples suggests that sulfidation was likely the dominant gold precipitation mechanism because it is considered to have destabilized gold-thiocomplexes in the ore-forming fluids. Based on textural relationships and chemical composition, arsenopyrite is interpreted to reflect two generations. Arsenopyrite 1 is possibly early in origin, sieve textured with abundant inclusions of pyrrhotite. Arsenopyrite 1 was then overgrown by late arsenopyrite 2 with no porous textures and rare inclusions of pyrrhotite. Gold mineralization was initiated by focused fluid flow and sulfidation of the oxide facies banded iron formation, leading to an epigenetic gold mineralization. The mineralogical assemblages, textures, and mineral chemistry data at the Tau gold deposit revealed two-stage gold mineralizations commencing with the deposition of invisible gold in arsenopyrite 1 followed by the later formation of native gold during hydrothermal alteration and post-depositional recrystallization of arsenopyrite 1. Laser ablation inductively coupled plasma mass spectrometric analysis of arsenopyrite from the Tau deposit revealed that the hydrothermal event responsible for the formation of late native gold also affected the distribution of other trace elements within the grains as evidenced by varying trace elements contents in arsenopyrite 1 and arsenopyrite 2. The range of δ34S of gold-bearing assemblages from the Tau deposit is restricted from +1.6 to +3.9‰, which is typical of Archean orogenic gold deposits and indicates that overall reduced hydrothermal conditions prevailed during the gold mineralization process at the Tau deposit. The results from this study suggest that gold mineralization involved multi-processes such as sulfidation, metamorphism, deformation, hydrothermal alteration, and gold remobilization. 相似文献
23.
Copper–Gold Skarn Mineralization at the Karavansalija Ore Zone,Rogozna Mountain,Southwestern Serbia 
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下载免费PDF全文 Zhivko D. Budinov Kotaro Yonezu Thomas Tindell Jillian Aira Gabo‐Ratio Stanoje Milutinovic Adrian J. Boyce Koichiro Watanabe 《Resource Geology》2015,65(4):328-344
Karavansalija ore zone is situated in the Serbian part of the Serbo‐Macedonian magmatic and metallogenic belt. The Cu–Au mineralization is hosted mainly by garnet–pyroxene–epidote skarns and shifts to lesser presence towards the nearby quartz–epidotized rocks and the overlying volcanic tuffs. Within the epidosites the sulfide mineralogy is represented by disseminated cobalt‐nickel sulfides from the gersdorfite‐krutovite mineral series and cobaltite, and pyrite–marcasite–chalcopyrite–base metal aggregates. The skarn sulfide mineralization is characterized by chalcopyrite, pyrite, pyrrhotite, bismuth‐phases (bismuthinite and cosalite), arsenopyrite, gersdorffite, and sphalerite. The sulfides can be observed in several types of massive aggregates, depending on the predominant sulfide phases: pyrrhotite‐chalcopyrite aggregates with lesser amount of arsenopyrite and traces of sphalerite, arsenopyrite–bismuthinite–cosalite aggregates with subordinate sphalerite and sphalerite veins with bismuthinite, pyrite and arsenopyrite. In the overlying volcanoclastics, the studied sulfide mineralization is represented mainly by arsenopyrite aggregates with subordinate amounts of pyrite and chalcopyrite. Gold is present rarely as visible aggregate of native gold and also as invisible element included in arsenopyrite. The fluid inclusion microthermometry data suggest homogenization temperature in the range of roughly 150–400°C. Salinities vary in the ranges of 0.5–8.5 wt% NaCl eq for two‐phase low density fluid inclusions and 15–41 wt% NaCl eq for two‐phase high‐salinity and three‐phase high‐salinity fluid inclusions. The broad range of salinity values and the different types of fluid inclusions co‐existing in the same crystals suggest that at least two fluids with different salinities contributed to the formation of the Cu–Au mineralization. Geothermometry, based on EPMA data of arsenopyrite co‐existing with pyrite and pyrrhotite, suggests a temperature range of 240–360°C for the formation of the arsenopyrite, which overlaps well with the data for the formation temperature obtained through fluid inclusion microthermometry. The sulfur isotope data on arsenopyrite, chalcopyrite, pyrite and marcasite from the different sulfide assemblages (ranging from 0.4‰ to +3.9‰ δ34SCDT with average of 2.29 δ34SCDT and standard deviation of 1.34 δ34SCDT) indicates a magmatic source of sulfur for all of the investigated phases. The narrow range of the data points to a common source for all of the investigated sulfides, regardless of the host rock and the paragenesis. The sulfur isotope data shows good overlap with that from nearby base‐metal deposits; therefore the Cu–Au mineralization and the emblematic base‐metal sulfide mineralization from this metallogenic belt likely share same fluid source. 相似文献
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Zhekai Zhou Kotaro Yonezu Akira Imai Thomas Tindell Huan Li Jillian Aira Gabo-Ratio 《Resource Geology》2022,72(1):e12279
The Woxi Au-Sb-W deposit is one of the largest polymetallic ore deposits in the Xuefengshan Range, southern China, hosted in low-grade metamorphosed Neoproterozoic volcaniclastic rocks. The orebodies of the deposit are predominantly composed of banded quartz veins, which are strictly controlled by bedding and faults. Petrographic observations and geochemical results are reported on the occurrence of Au and properties of the ore-forming processes for different stages in the deposit. The veins extend vertically up to 2 km without obvious vertical metal zoning. The ore-forming process can be subdivided into four mineralization stages: Pre-ore stage; Early stage (scheelite-quartz stage); Middle stage (pyrite-stibnite-quartz stage); and Late stage (stibnite-quartz sage). Four types of pyrite (Py0, Py1, Py2, and Py3) were identified in the ores and host-rock: Py0 occurs as euhedral grains with voids in the core, ranging in size from 50 to 100 μm and formed mainly in the Pre-ore stage and Early stage; Py1 occurs as subhedral grains. Small grains (around 10 μm) of Py1 form irregularly shaped clusters of variable size ranging from tens to hundreds of μm and mainly formed in the Middle stage; Euhedral-subhedral fine-grained Py2 formed in the Late stage; Minor subhedral fine-grained Py3 was deposited in the Late-stage. Stibnite is widely distributed in the Middle and Late stage ore veins. No systemic difference was recognized in mineralogical features among stibnite formed in different stages. In addition to native gold, the lattice bound Au+1 widely exists in Py1 and Py2 in the deposit, and widespread Py1 is considered as the main Au-bearing mineral with the highest Au contents. Most elements (such as Co, Ni, Cu, As, Sb, Ba, and Pb) are considered to occur as solid solution within the crystal lattice and/or invisible nanoparticles in sulfides minerals. The Co/Ni ratio of most pyrite is lower than 1, suggesting that the metals in the ore-forming fluid are sourced from sedimentary rocks. The coupled behavior between Au and As; Au and Sb suggests that the substitution of As and Sb in pyrite can enhance the incorporation of Au. Variation of trace elements in pyrites of different stages suggests some information on the mineralization processes: Large ion lithophile elements (such as Ba and Pb) are enriched in Py0 indicating that water-rock reaction occurred in the Early stage; Fine-grained Py1 with a heterogeneous distribution of elements suggests fast crystallization of pyrite in the Middle stage. 相似文献
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Akira Imai Kotaro Yonezu Kenzo Sanematsu Takashi Ikuno Shingo Ishida Koichiro Watanabe Visut Pisutha‐Arnond Somchai Nakapadungrat Jarupong Boosayasak 《Resource Geology》2013,63(1):84-98
Geochemical studies were conducted on the hydrothermally altered granitic rocks in the Ranong and Takua Pa tin‐fields in southern Thailand in order to investigate the mode of occurrence of REE (rare earth elements), with emphasis placed on a potential REE resource associated with granitic rocks in the Southeast Asian Tin Belt. The total REE (ΣREE) content of altered granitic rocks ranges from 130 to 350 ppm at Haad Son Paen (which is presently mined for kaolin clay) in the Ranong tin‐field, and that of altered granitic rocks and kaolinite veinlets reaches up to 424 ppm and 872 ppm, respectively, at Nok Hook in the Takua Pa tin‐field. Rare earth elements in the altered granitic rocks and kaolinite veinlets show a relatively flat chondrite‐normalized pattern, thus enriched in heavy REE compared with the original granitic rocks and their weathered crusts. At Nok Hook (Takua Pa), the ΣREE content of kaolinite separated from an altered granitic rock by elutriation is 1313 ppm, a ΣREE amount about four times higher than that of whole‐rock composition of the altered granitic rock. Chondrite‐normalized REE patterns of the elutriated kaolinite and of the altered granite are relatively flat. Sequential extraction experiments suggest that 41 and 85 percent of REE are present as ion exchangeable‐form in the altered granitic rock, and in the kaolinite veinlets, respectively. In addition, more than 90% of REE in the kaolinite veinlets are present as the acid‐soluble state. On the other hand, the ΣREE content of kaolinite veinlets and of the kaolinite concentrated by elutriation from an altered granitic rock at Haad Som Paen (Ranong) is 70 ppm and 75 ppm, respectively, thus enrichment of REE in kaolinite was not confirmed. In addition, by the sequential extraction experiments, 23% and 4% of REE were extracted from the altered granitic rock and the kaolinite veinlets at Haad Som Paen. In the altered granitic rocks at Haad Som Paen, REE are present as refractory phases, and REE in the acid‐soluble states had been leached by hydrothermal fluid. 相似文献
27.
Naoto Takahata Yuji Sano Keika Horiguchi Kotaro Shirai Toshitaka Gamo 《Journal of Oceanography》2008,64(2):293-301
We have collected fifty-five seawater samples at seven stations at various depths in the Yamato and Japan Basins of the Japan
Sea and measured their helium isotopic ratios. The 3He/4He ratios vary from 0.997 Ratm to 1.085 Ratm where Ratm is the atmospheric ratio. The maximum 3He excesses about 8%, are observed at mid-depth (1000 m), and these values are significantly lower than those observed in
deep Pacific waters. This implies that mantle-derived helium in deep Pacific water cannot enter the Japan Sea since it is
an almost landlocked marginal sea. The observed 8% excess 3He may be attributable to the decay product of tritium. Slightly higher 3He/4He ratios in the Bottom Water were observed in the Yamato Basin than in the Japan Basin. The ventilation ages of seawater
shallower than 1000 m are calculated as about 5 to 20 years, which is consistent with the CFC ages reported in the literature.
There is a positive correlation between the apparent oxygen utilization and 3H-3He ages. The estimated oxygen utilization rate from the correlation in a layer between 500 m and 1000 m is about 3 μmol/kg/yr, which is similar to that in the eastern subtropical North Atlantic. 相似文献
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Yuki Tohma Akira Imai Kenzo Sanematsu Kotaro Yonezu Ryohei Takahashi Masaaki Koyama Ryota Sekine Robert Duncan Koichiro Watanabe 《Resource Geology》2010,60(4):348-358
The Fukusen No. 1 vein is located in the southeastern part of the Yamada deposit, Hishikari epithermal gold deposits, southern Kyushu, Japan. 40Ar/39Ar plateau ages of adularia from the margin and the center of the Fukusen vein are determined to be 0.617 ± 0.024 Ma and 0.606 ± 0.009 Ma, respectively. The Fukusen No. 1 vein shows banding structure composed mainly of quartz, adularia and clay minerals. Colloform texture is displayed by cryptocrystalline to amorphous silica material that is associated with fine-grained electrum and sulfides near the center of the vein. Pyrite in the Fukusen No. 1 vein often shows acicular shape resulting from inversion from marcasite. Near the center of the vein, primary marcasite occurs associated with colloform texture of silica. The Fukusen No.1 vein preserves primary texture and materials which were deposited from the ore-forming hydrothermal solution. The Fukusen No. 1 vein was formed in a short period and is one of the youngest veins in the Hishikari deposits. 相似文献
30.
Ichiro Takeuchi Kaoruko Mizukawa Tokutaka Ikemoto Kotaro Tsuchiya 《Marine pollution bulletin》2009,58(5):663-9029
Biomagnification profiles of polycyclic aromatic hydrocarbons (PAHs), alkylphenols, and polychlorinated biphenyls (PCBs) from the innermost part of Tokyo Bay, Japan were analyzed using stable carbon (δ13C) and nitrogen (δ15N) isotope ratios as guides to trophic web structure. δ15N analysis indicated that all species of mollusks tested were primary consumers, while decapods and fish were secondary consumers. Higher concentrations of PCBs occurred in decapods and fish than in mollusks. In contrast, concentrations of PAHs and alkylphenols were lower in decapods and fish than in mollusks. Unlike PCBs, whose concentrations largely increased with increasing δ15N (i.e. increasing trophic level), all PAHs and alkylphenols analyzed followed a reverse trend. Molecular weights of PAHs are lower than those of PCBs, therefore low membrane permeability caused by large molecular size is an unlikely factor in the “biodilution” of PAHs. Organisms at higher trophic levels may rapidly metabolize PAHs or they may assimilate less of them. 相似文献