• Economic and Environmental Geology
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• v.45 no.6
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• pp.623-641
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• 2012

The Janggun lead-zinc-silver deposit is hydrothermal-metasomatic deposit. We have sampled wallrock, hydrother-maly-altered rock and lead-zinc-silver ore vein to study the element dispersion during wallrock alteration. The hydrothermal alteration that is remarkably recognized at this deposit consists of rhodochrositization and dolomitization. Wallrock is dolomite and limestone that consisit of calcite, dolomite, quartz, phlogopite and biotite. Rhodochrosite zone occurs near lead-zinc-silver ore vein and include mainly rhodochrosite with amounts of calcite, dolomite, kutnahorite, arsenopyrite, pyrite, chalcopyrite, sphalerite, galena and stannite. Dolomite zone occurs far from lead-zinc-silver ore vein and is composed of mainly dolomite and minor calcite, rhodochrosite, pyrite, sphalerite, chalcopyrite, galena and stannite. The correlation coefficients among major, trace and rare earth elements during wallrock alteration show high positive correlations(dolomite and limestone = $Fe_2O_3(T)$/MnO, Ga/MnO and Rb/MnO), high negative correlations(dolomite = MgO/MnO, CaO/MnO, $CO_2$/MnO, Sr/MnO; limestone = CaO/MnO, Sr/MnO). Remarkable gain elements during wallrock alteration are $Fe_2O_3(T)$, MnO, As, Au, Cd, Cu, Ga, Pb, Rb, Sb, Sc, Sn and Zn. Remarkable loss elements are CaO, $CO_2$, MgO and Sr. Therefore, elements(CaO, $CO_2$, $Fe_2O_3(T)$, MgO, MnO, Ga, Pb, Rb, Sb, Sn, Sr and Zn) represent a potential tools for exploration in hydrothermal-metasomatic lead-zinc-silver deposits.

• Economic and Environmental Geology
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• v.42 no.6
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• pp.513-525
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• 2009

The Buyeong gold-silver deposit consists of quartz veins that fill along the NS fault zone within Cretaceous Goseong formation. Mineralization can be divided into hypogene and supergene stages. Hypogene stage is associated with hydrothermal alteration minerals such as sericite, pyrite, chlorite, epidote and sulfides such as pyrite, pyrrhotite, marcasite, sphalerite, chalcopyrite, galena and galenobismutite. Supergene stage is composed of malachite, goethite, chalcocite, and sphalerite oxide. Fluid inclusion data indicate that homogenization temperatures and salinities range from 112 to $340^{\circ}C$ and from 0.2 to 7.9 wt.% NaCl, respectively. Sulfur(3.2~3.9‰) isotope composition indicates that ore sulfur was derived from mainly magmatic source as well as partly host rocks. The calculated oxygen(4.3~6.0‰) and hydrogen(-60~-64‰) isotope compositions indicate that hydrothermal fluids may be meteoric origin with some degree of mixing of another meteoric water for paragenetic time.

• The Journal of the Petrological Society of Korea
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• v.11 no.2
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• pp.90-102
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• 2002

The studied Fe-REE ore consists of magnetite, ankerite, siderite, magnesite and strontianite as the major constituent, and monazite, columbite, fergusonite, apatite, aegirine-augite, Na-amphibole, pyrite, chalcopyrite, sphalerite, molybdenite and barite as accessaries. Wall rock of ore deposits is replaced to fenite due to Na-metasomatism and mainly consists of sugary albite and Na-amphibole. Monazite $Ce_{0.49}La_{0.31}Pr_{0.14}Nd_{0.03}Gd_{0.03})PO_4$ is the main mineral for REE deposit and shows myrmekitic intergrowth with strontianite $Ca_{0.02-0.16}Sr_{0.84-0.98}CO_3$ and is corroded by carbonate minerals. Mineral forming sequence can be divided into early and late periods by the development of microfractures. The early period minerals such as magnetite, ankerite, magnesite, monazite and apatite show well developed networks of microfractures due to cataclastic deformation caused by enriched $CO_2$ gas in melts during emplacement. The late minerals of columbite, fergusonite, siderite molybdenite, chalcopyrite and sphalerite formed after the brecciation event and have little micro-fractures. Ankerite, magnesite, monazite, strontianite, barite and pyrite seem to be formed continuously from the ealy to the late period since they show textures both with well developed fractures and also with little fractures. Mineral chemistry, mineral assemblages such as various carbonate minerals, magnetite, REE minerals of monazite and fergusonite, Sr mineral of strontianite, and Nb minerals of columbite, myrmekitic texture of monazite and ankerite, and well developed fenite along ore deposits observed from this studied area strongly indicate that this Hongcheon Fe-REE ore deposits are formed from carbonatitic melt and its rock type is late differentiated Fe-carbonatite or ankerite-carbonatite.

• Journal of the Mineralogical Society of Korea
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• v.19 no.4 s.50
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• pp.337-346
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• 2006

The Jinwon Pb-Zn deposit is located within the Precambrian Youngnam Massif. Ore mineralization at the Jinwon deposit occurred in quartz veins that filled fractures in the Hongjesa granite. Mineral paragenesis can be divided into two stages(stage I and II). Stage I, at which the precipitation of major ore minerals occurred, is further divided into two substages with paragenetic time based on minor fractures and discernible mineral assemblages: substage la is characterized by pyrite, arsenopyrite ($28.4{\sim}30.3$ atomic % As), pyrrhotite, magnetite, chalcopyrite, sphalerite ($13.1{\sim}16.0$ mole % FeS) assemblages; substage $I_a$ is represented by main precipitation of Zn, Pb minerals and is characterized by sphalerite ($15.1{\sim}19.0$ mole % FeS), galena, miargyrite, argentile assemblages. Stage II is economically barren quartz veins. Thermodynamics study is used to estimate changes in chemical conditions of the hydrothermal fluids during stage I mineralization, the main ore deposition period at the Jinwon hydrothermal system. The range of estimated sulfur fugacity ($fs_2$) was from $10^{-7}\;to\;10^{-16}$ atm and oxygen fugacity ($fo_2$) was in the range of $10^{-32.8}{\sim}10^{-38.5} atm$. Carbon dioxide fugacity ($fco_2$) was $<10^{-0.6} atm$.

• Journal of the Mineralogical Society of Korea
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• v.21 no.1
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• pp.1-15
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• 2008

The Cretaceous Gajok gold-silver deposit within porphyry granite is located nearby the Cretaceous Pungam basin at the northeastern area in Republic of Korea. The Gajok gold-silver deposit is distinctively composed of a multiple-complex hydrothermal veins with comb, crustiform chalcedony quartz and vug textures, implying it was formed relatively shallower depth. The hypogene open-space filling veins could be divided into 5 paragenetic sequences, increasing tendency of Ag-rich electrum and Ag-phases with increasing paragenetic time. Electrum with high gold contents (${\sim}50$ atomic % Au) as well as sphalerite with high FeS contents (${\sim}6$ mole % FeS) are representative ore minerals in the middle stage. The late stage is characterized by silver-phase such like native silver and/or argentite, coexisting with Ag-rich electrum ($10{\sim}30$ atomic % Au) and Fe-poor sphalerite (< 1 mole % FeS). The ore-forming fluids evolution started at relatively high temperature and salinity (${\sim}360^{\circ}C$, ${\sim}7\;wt.%$ eq. NaCl) and were evolved by dilution and mixing mechanisms on the basis of fluid inclusion study. The gold-silver mineralization proceeded from ore-forming fluids containing greater amounts of less-evolved meteoric waters(${\delta}^{18}O$; $-0.6{\sim}-6.7\;%o$). These results imply that gold-silver mineralization of the Cretaceous Gaiok deposit formed at shallow-crustal level and could be categorized into low-sulfidation epithermal type, related to Cretaceous igneous activity.

• Journal of the Mineralogical Society of Korea
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• v.31 no.2
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• pp.87-101
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• 2018

The Manjang deposit developed in the Hwajeonri formation of the Okcheon metamorphic belt consists of the Central and Main orebodies of Cu-bearing hydrothermal vein type and the Western orebody of Fe-skarn type. This study focuses on the Cu mineralization of the Central and Main orebodies to compare with the genetic environments of the Western orebody previously studied. The Central orebody produced pyrrhotite and chalcopyrite as major ore minerals with vein texture, while the Main orebody contains pyrite, arsenopyrite, and chalcopyrite as major ore minerals with vein, massive, and brecciated texture. Sphalerite, galena, magnetite, ilmenite, rutile, cassiterite, wolframite, and stannite are also accompanied. Local occurrence of skarn is dominated by grossular and hedenbergite, reflecting the reduced condition of the skarnization. Geothermometries of sphalerite-stannite in the Central orebody and arsenopyrite-pyrite in the Main orebody indicate the formation temperature of $204-263^{\circ}C$ and $383-415^{\circ}C$, respectively. Sulfur fugacity of $10^{-6}-10^{-7}atm$. in the Main orebody decreased toward the Central orebody. Sulfur isotope compositions of sulfide minerals from the Central and Main orebodies are 4.6-7.9‰ and 4.3-7.0‰, respectively, reflecting magmatic origin with slight influence by host rock. Considering ore mineralogy, texture as well as physicochemical conditions, the Main and Central orebodies of hydrothermal Cu mineralization reflect the characteristics of proximal and distal type ore mineralization, respectively, related to hidden igneous rocks, and they were generated under different hydrothermal systems from the Fe-skarn Western orebody.

• Economic and Environmental Geology
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• v.32 no.2
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• pp.129-139
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• 1999

Hydrothermal gold deposits of the Trabong district in Vietnam occur as single-stage quartz $\pm$ calcite veins (0.3-1.2 m thick) which fill fault fractures in graphite-bearing gneiss and schist of the Chulai Complex and Kham Duc Formation of the Proterozoic age. Ore grades are 1.3 to 92.4 g/ton Au. Ore mineralogy is very simple, consisting mainly of pyrite with minor amounts of base-metal sulfides and electrum. Gold grains occur in two assemblages as follows: (1) early, Fe-rich (7.2-10.4 mole % FeS) sphalerite + electrum (50.4-64.3 atom % Au) assemblage occurring as inclusions in pyrite; (2) late, Fe-poor «4.7 mole % FeS) sphalerite + galena + electrum (47.6-81.7 atom % Au) assemblage occurring along fractures of pyrites. Based on fluid inclusion data and thermochemical considerations of ore mineral assemblages, ore minerals were formed at high temperatures (about $230^{\circ}C$ to $420^{\circ}C$) from $H_{2}O-CO_{2}(-CH_{4})$-NaCI fluids with the sulfur fugacity of about $10^{-6}$ to $10^{-10}$ atm. Fluid inclusion data also indicate that ore mineralization occurred mainly as a result of fluid unmixing accompanying $CO_2$ effervescence. Calculated oxygen and measured hydrogen isotope compositions of mineralizing waters (${\delta}^{18}O_{V-SMOW}$ values = 5.3 to 8.6$\textperthousand$, ${\delta}D_{V-SMOW}$ values = - 60 to - 52$\textperthousand$), along with the sulfur isotope compositions of vein sulfides (${\delta}^{34}S_{CDR}$ values = - 1.2 to 2.8$\textperthousand$) and carbon isotope compositions of inclusion $CO_2$ (${\delta}^{13}C_{PDB}$ values = - 4.7 to - 2.0$\textperthousand$) indicate that the high temperature (mesohypothermal) gold mineralization formed from a magmatic fluid.

• Journal of the Mineralogical Society of Korea
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• v.21 no.4
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• pp.383-395
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• 2008

To enhance the grade and recovery rate of the gold/silver ores which yield at Philippine Mankayan mine, we studied the characteristics which are the geologic and mineralogical features of gold and silver ore, the liberation by crushing and grinding, the separation by sieving and shaking table. Gold/silver ore is composed of the sulfide minerals like pyrite, sphalerite, galena; and the gangue minerals which is quartz, clay. Gold/silver element are mainly contained in a sulfide minerals like pyrite, sphalerite and galena. To increase the liberation rate of sulfide minerals containing gold/silver element, the gold/silver ore has to be grounded under $100{\mu}m$ very finely because the crystal size of sulfide minerals is distributed from $1{\mu}m$ to $100{\mu}m$. The liberation rate of gold/silver ore increases to 92% when the particle size ($d_{90}$) of ore is grounded below $100{\mu}m$ by jaw crusher $\to$ cone crusher $\to$ rod mill by steps. The grade and recovery of sulfide minerals could not be enhanced by sieving separation because those crystal size is distributed homogeneously below $100{\mu}m$. But, when we separated the sieved ore using shaking table, the gold and silver grade increased to 40 ppm and 140 ppm, respectively. Then the recovery rate of gold reach almost 100% but that of silver is no more that 50%.

• Geophysics and Geophysical Exploration
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• v.17 no.4
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• pp.247-252
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• 2014

Gagok Mine, which is skarn deposits, includes sulfide minerals such as sphalerite, galena, chalcopyrite, and pyrrhotite. To explore these minerals, spectral induced polarization (SIP) is relatively effective compared to other geophysical exploration methods because there is a strong IP effect caused by electrode polarization. In the SIP, the chargeability related to sulfide mineral contents and the time constant related to the grain size of the minerals are obtained. For this reason, we aim to compare difference in the mineralized characteristics between two orebodies in the Gagok Mine by using the chargeability and the time constant. For this study, we sampled ores from the south of Wolgok orebody and the north of Sungok orebody. In order to recognize the mineralization characteristics, the metal content of the samples was measured by a potable XRF and the SIP data of the samples were acquired by using a laboratory SIP measurement system. As a result, the metals in the samples such as Pb, Zn, Cu, and Fe were detected by the portable XRF measurement. In particular, the Fe and Zn contents were far higher than the other metals. The Fe and the Zn were caused by the sphalerite and the pyrrhotite through microscopy. The Wolgok orebody had higher sulfide mineral contents than the Sungok orebody and the result corresponded with the chargeability result. However, we considered that the Sungok orebody had a larger sulfide mineral grain size than the Wolgok orebody because the time constant of the Sungok orebody was larger.

• Journal of the Mineralogical Society of Korea
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• v.20 no.2 s.52
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• pp.115-124
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• 2007

Electrum-sulfide mineralization of the Youngbogari mine area occurred in two stages of massive quartz veins that fill the fractures along the fault/shear zones in the Precambrian gneiss. Ore mineralogy is simple, consisting of arsenopyrite $(31.4{\sim}33.4atom.%As)$, pyrite, sphalerite $(4.1{\sim}17.6mole%FeS)$, galena, chalcopyrite, argentite, and electrum. Electrum $(60.3{\sim}87.6atom.%Ag)$ is associated with galena, chalcopyrite and late sphalerite infilling the fractures in quartz and sulfides. Fluid inclusion data show that ore mineralization was formed from $H_2O-CO_2-CH_4-NaCl$ fluids $(X_{CO2+CH4}=0.0\;to\;0.2)$ with low salinities (0 to 10wt.% eq. NaCl) at temperatures between $200^{\circ}\;and\;370^{\circ}C$. Gold-silver mineralization occurred later than the base-metal sulfide deposition, at temperatures near $250^{\circ}C$ and was probably a result of cooling and decreasing sulfur fugacity caused by sulfide precipitation and/or $H_2S$ loss through fluid unmixing.