• Economic and Environmental Geology
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• v.19 no.3
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• pp.199-218
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• 1986

Arsenopyrite in arsenic and polymetallic ores from calcic Fe-W skarn deposit of the Ulsan mine, Republic of Korea, has been investigated by means of electron microprobe analysis and X-ray diffractometry. As a result, it is revealed that the Ulsan arsenopyrite may be classified into the following three species with different generation on the basis of its mode of occurrence, chronological order during polymetallic mineralization and chemical composition; arsenopyrites I, II and III. 1) Arsenopyrite I-(Ni, Co)-bearing species belonging to the oldest generation, which has crystallized together with (Ni, Co)-arsenides and -sulpharsenides in the early stage of polymetallic mineralization. In rare cases, it contains a negligible amount of antimony. It occurs usually as discrete grains with irregular outline, showing rarely subhedral form, and is diffused in skarn zone. The maximum contents of nickel and cobalt are 10.04 Ni and 2.45 Co (in weight percent). Occasionally, it shows compositional zoning with narrow rim of lower (Ni+Co) content. 2) Arsenopyrite II-arsenian species, in which (Ni+Co) content is almost negligible, may occur widely in arsenic ores, and its crystallization has followed that of arsenopyrite I. It usually shows subhedral to euhedral form and is closely associated with $l{\ddot{o}}llingite$, bismuth, bismuthinite, chalcopyrite, sphalerite, bismuthian tennantite, etc. It is worthy of note that arsenopyrite II occasionally contains particles consisting of both bismuth and bismuthinite. 3) Arsenopyrite III-(Ni, Co)-free, S-excess and As-deficient species is close to the stoichiometric composition, FeAsS. It occurs in late hydrothermal veins, which cut clearly the Fe-W ore pipe and the surrounding skarn zone. It shows euhedral to subhedral form, being extremely coarse-grained, and is closely associated with pyrite, "primary" monoclinic pyrrhotite, galena, sphalerite, etc. Among three species of the Ulsan arsenopyrite, arsenopyrite I does not serve as a geothermometer, because (Ni+Co) content always exceeds 1 weight percent. In spite of the absence of Fe-S minerals as sulphur-buffer assemblage, the presence of $Bi(l)-Bi_2S_3$ sulphur-buffer enables arsenopyrite II to apply successfully to the estimation of either temperature and sulphur fugacity, the results are, $T=460{\sim}470^{\circ}C$, and log $f(S_2)=-7.4{\sim}7.0$. With reference to arsenopyrite III, only arsenopyrite coexisting with pyrite and "primary" monoclinic pyrrhotite may serve to restrict the range of both temperature and sulphur fugacity, $T=320{\sim}440^{\circ}C$, log $f(S_2)=-9.0{\sim}7.0$. These temperature data are consistent with those obtained by fluid inclusion geothermometry on late grandite garnet somewhat earlier than arsenopyrite II. At the beginning of this paper, the geological environments of the ore formation at Ulsan are considered from regional and local geologic settings, and physicochemical conditions are suspected, in particular the formation pressure (lithostatic pressure) is assumed to be 0.5kb (50MPa). The present study on arsenopyrite geothermometry, however, does not bring about any contradictions against the above premises. Thus, the following genetical view on the Ulsan ore deposit previously advocated by two of the present authors (Choi and Imai) becomes more evident; the ore deposit was formed at shallow depth and relatively high-temperature with steep geothermal gradient-xenothermal conditions.

• Economic and Environmental Geology
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• v.56 no.3
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• pp.239-257
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• 2023

Sangdong deposit, a W-Mo skarn deposit, is located in Taebaeksan mineralized district, hosting vertically developed scheelite-quartz veins that formed at the late ore-forming stage. In this study, we tried to examine the geochemical signatures of ore-forming fluids and vein-forming mechanisms by analyzing the micro-texture of quartz veins and trace element concentrations of quartz. As a result of texture analyses, quartz veins in the hanging wall orebody and the foot wall orebody commonly exhibit the blocky and the elongate blocky texture, respectively, whereas quartz veins in the main orebody show both textures. These textural differences indicate that quartz veins from the hanging wall orebody were precipitated by the primary hydrofracturing due to H₂O saturation in the igneous body with relatively high temperature and pressure at a vein-skarn stage, and after that, repeated hydrofracturing caused the formation of quartz veins from the main orebody and foot wall orebody. The results of trace element concentrations show that Li⁺+Al³⁺↔Si⁴⁺ is a main substitution mechanism. However, those of the foot wall orebody were clearly divided into a Li⁺-dominated substitution and a Na⁺-, K⁺-dominated substitution. Considering that quartz veins from the foot wall orebody commonly show the elongate blocky texture, such a distinction means that it is a result of repeated injections of fluid with the different composition. Ti concentrations of quartz from the hanging wall, main, and the foot wall orebody are 28.6, 8.2, and 15.7 ppm in average, respectively. Given a proportional relationship between the precipitation temperature and Ti concentrations, it seems that quartz veins from the hanging wall orebody were precipitated at the highest temperature. Al concentrations of the hanging wall, main, and the foot wall orebody having an inverse relationship with fluid pH are 162.3, 114.2, and 182.5 ppm in average, respectively. These results show that Al concentrations in vein-forming fluids were not changed dramatically. Moreover, these concentrations are extremely low in comparison with the other hydrothermal deposits. This indicates that quartz in overall ore veins at Sangdong deposit was precipitated from the constant condition with slightly acidic to near neutral pH.

• Economic and Environmental Geology
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• v.48 no.2
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• pp.169-175
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• 2015

Silver production in Peru was 118 Moz in 2013, which was $3^{rd}$ ranked in the world. Silver production mines which were ranked from $1^{st}$ to $5^{th}$ in Peru in 2013 were Antamina(16.7 Moz), Uchuchacua(12 Moz), Pallancata(7.6 Moz), Anim$\acute{o}$n(7 Moz), and Arcata(5.4 Moz). Total reported silver resources in Peru is about 7,012 Moz, and resources from the belts of Miocene epithermal deposits and the belts of Miocene skarn, replacement and vein deposits are 4,812 Moz, which corresponds to 69% of total resources. There are 14 ongoing projects which will be developed to the production stage from 2014 to 2019. Through these projects, silver production in Peru is expected to be 148 Moz in 2017.

• Economic and Environmental Geology
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• v.44 no.1
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• pp.1-10
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• 2011

The geology of the Pacitan district which occupies Southern mountain zone in the southwestern margin of East Java, Indonesia, consists of a pile of clastics and pyroclastics grading upwards into a series of sediments of Middle Miocene age which are intruded by a number of quartz porphyries and subvolcanic dacitic to andesitic bodies in after that time. The geochemical exploration in the Pacitan district to find out anomalous areas related with metallic mineral dispersion from the concealed ore deposits had been carried out using traditional exploration techniques of geological mapping, stream sediment, panned concentrate and outcrop sampling. The anomalous zones of each element were detected in the following areas: Gempol for Cu; Jompong for Au; Kasihan for Cu-Pb-Zn. The strongest Cu-Pb-Zn anomalous values are overlapped at the Kasihan area. The geochemical survey of soil was conducted with the geological survey at the Kasihan area. The statistical values were calculated by the statistical analysis method. The patterns for Cu, Pb and Zn are similar to the normal distribution. The anomalous values of copper-lead-zinc and/or copper and zinc are overlapped at five zones surrounding quartz porphyry at the central part of the Kasihan area. The area was interpreted and chosen as an anomalous zone related with stockwork and skam mineralization, extending to approximately NNW-SSE direction.

• Journal of the Mineralogical Society of Korea
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• v.16 no.1
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• pp.49-63
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• 2003

Rare and unusual occurrence of hydrothermal minerals were found in Geode mine area. They are developed in the late stage of hydrothermal alteration of earlier skarns and later by the open-space filling crystallization. The alteration of earlier skarns of clinopyroxene, garnet, and plagioclase formed mainly chlorite or sometimes uncommon hydrothermal minerals of prehnite, illite, and pumpellyite. Open-space filling crystallization characterized by hydrothermal minerals developedin open sapce or good are prehnite, pumpellyite, clinozoisite, illite, and Ca-zeolites of stilbite annstellerite. Mineral phases and paragenesis are examined in detail by microscopy, XRD, SEM, and EPMA. Using the Schreinemaker's method, equibrium reactions among these minerals are establishedand isothemal-isobaric phase diagrams of $\mu$$H_2O$-$\mu$$CO_2$cot are plotted. Hydrothermal minerals such asprehnite, pumpellyite, clinozoisite, illite, and some chlorite were ffrmed under high partial pressure of $CO_2$with relatively low $H_2$O fugacity. Later, stilbite and calcite in association with illite crystallized under relatively both high partial Pressure of $CO_2$and high $H_2$O fugacity.

• Economic and Environmental Geology
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• v.16 no.1
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• pp.1-10
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• 1983

The Yeonhwa (I, II) and Keodo mines, neighboring in the middle part of the Taebaegsan mineral belt, contain three distinct classes of skarn deposits: the zinc-lead skarn at Yeonhwa (I, II), the iron skarn at Keodo south (Jangsan orebodies), and the copper skarn at Keodo north (78 orebodies). The present study characterizes the three classes of skarn deposits mainly in terms of skarn/ore associations examined from chemical compositional point of view, and applies existing quantitative phase diagrams to some pertinent mineral assemblages in these mines. At Yeonhwa I the Wolam I orebody shows a vertical variation in skarn minerals ranging from clinopyroxene/garnet zone on the lower levels through clinopyroxene (without garnet) zone on the intermediate levels, and finally to rhodochrosite veins on the upper levels and surface. Ore minerals, sphalerite and galena, associate most closely with the intermediate clinopyroxene zone. At Keodo, the Jangsan iron skarn hosted in quartz monzodiolite as a typical endoskarn, shows a skarn zoning, from center of orebody to outer side, magnetite zone, magnetite/garnet zone, garnet clinopyroxene zone, and clinopyroxene/epidote/plagioclase zone. The 78 copper skarn in the Hwajeol limestone indicates a zoning, from quartz porphyry side toward limestone side, orthoclase/epidote zone, epidote/clinopyroxene zone, and clinopyroxene/garnet zone; chalcopyrite and other copper sulfides tend to be in clinopyroxene/garnet zone. Mioroprobe analyses of clinopyroxenes and garnets from the various skarn zones mentioned above revealed that the Yeonhwa zinc/lead skarns are characterized by johansenitic clinopyroxene (Hd 25-78, Jo 15-23) and manganoan andraditic garnet (Ad 13-97, Sp 1-24), whereas the Jangsan iron skarn at Keodo by Mn-poor diopsidic clinopyroxene (Di 78-93, Jo 0.2-1.0) and Mn-poor grossularitic grandite (Gr 65-77, Sp 0.5-1.0). The 78 copper skarn at Keodo is characterized by Mn-poor diopsidic-salite (Di 66-91, Jo 0.2-1.1) and Mn-poor andraditic grandite(Ad 40-74, Sp 0.5-1.1). The compositional charateristics of iron, copper, and zinc-lead skarns in the Yeonhwa-Keodo mines are in good correlations with those of the foreign counterparts. Compiling a $T-XCO_2$ phase diagram for the Jangsan endoskarns, a potential upper limit of temperature of the main stage of skarn formation is estimated to be about $530^{\circ}C$, and a lower limit to be $400^{\circ}C$ or below assuming $XCO_2=0.05$ at P total=1kb. Applying a published log $fS_2$-log $fo_2$ diagram to the Keodo 78 and Yeonhwa exoskarns, it is revealed that copper sulfides and zinc-lead sulfides do not co-exist stably below log $fS_2=-4$ and log $fO_2=-23$ at $T=400^{\circ}C$ and ${\times}CO=1$ atm.

• Journal of the Mineralogical Society of Korea
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• v.19 no.4 s.50
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• pp.325-336
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• 2006

Domestic serpentinite is one of the important industrial minerals utilizing in the iron manufacturing company such as POSCO in Korea. Serpentinite is distributed in the Ulsan Fe deposit, Andong, Hongseong-Cheongyang, and Gapyeong areas. This study tries to interpret the relationship among the formation of carbonate rocks, iron mineralization, and serpentinite alteration throughout the study of field occurrence, mineralogy, and chemical compositions. Serpentine is formed by the break-down of olivine and pyroxene of parent peridotite. The serpentinization is inferred to be formed by the hydrothermal fluid derived from intruded Cretaceous granite and the addition of meteoric water. Variation of major oxides such as $SiO_2,\;Fe_2O_3$, and MgO in serpentinized rocks are controlled by the degree of serpentinization and Fe mineralization. Variation of $Al_2O_3$ and CaO contents of altered rocks is dependent on the amount of the residual minerals such as calcite and homblende, and on the degree of chloritization. The presence of carbonate rocks reported in the sedimentary origin or igneous origin (carbonatite) provided a geological environment to form skarn type Fe deposit regardless of its origin. The geological processes of Ulsan Fe deposits are inferred to be formed as the order of the formation of carbonate rocks ${\to}$ the intrusion of Cretaceous granite ${\to}$ serpentinization ${\to}$ Fe mineralization by the interprelation of field occurrence and mineralogical characteristics.

• Economic and Environmental Geology
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• v.25 no.1
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• pp.1-16
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• 1992

The Wondong Fe-Pb-Zn deposit is located in endo and exoskarns formed along the contact between the Makkol limestone interbedding pelitic limestone of Ordovician age and quartz porphyry of Cretaceous age. At the Wondong mine, the endoskarn shows a discontinuous zonal arrangement from quartz porphyry to pelitic limestone as follows: unaltered quartz porphyry, weakly altered quartz porphyry zone, intensively altered pinkish quartz porphyry zone, garnet zone, and greyish white and fine-grained clinopyroxene zone developed at pelitic limestone side. In terms of chemical mass balance, intensively altered pinkish quartz porphyry relative to unaltered quartz porphyry shows substantial enrichments in $K_2O$, $Na_2O$, and HREE and depletions in MgO, CaO, total $Fe_2O_3$, and LREE. On the other hand, garnet zone of endoskarn is enriched in CaO, MnO, total $Fe_2O_3$, MgO and depleted in $K_2O$, $Na_2O$. $Al_2O_3$ seems to be determining inert component. Thus the behavior of elements indicates that the mobility of elements depends on the equilibration of hydrothermal fluid and minerals and affects on enrichments by fractionation from and depletions by partition to hydrothermal fluid, respectively. Traversing toward pelitic limestone from a central zone of exoskarn, the exoskarn also shows a zonal arrangement as follows: garnet zone, clinopyroxene zone, and decolored pelitic limestone. The arrangement of mineral assemblages in skarns of the Wondong mine is the result of an increase in CaO and $K_2O$ toward the pelitic limestone. Skarn and ore minerals were formed in the following sequence: early skarn, late skarn and magnetite, pyrite, sphalerite, galena, and molybdenite. On the basis of stabilities of mineral assemblages, physicochemical conditions of the late skarn and magnetite mineralization are estimated to be $350^{\circ}C{\leq}T{\leq}400^{\circ}C$ at 1 Kb, $-23{\leq}log\;fO_2{\leq}-18$, and $0.005{\leq}XCO_2{\leq}0.01$, while those of the early skarn to be $420^{\circ}C{\leq}T{\leq}550^{\circ}C$ at 1 Kb.

• Economic and Environmental Geology
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• v.50 no.1
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• pp.73-83
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• 2017

The surveyed mines are located in a polymetallic vein, replacement, and skarn mineral district in the central Andes of Peru. Iscaycruz, which includes underground and open pit mines that produce zinc and lead concentrates, was the largest mineral deposit of an important group of base metal deposits in the Andes of central Peru. The deposits are sub-vertical seams of polymetallic ores(Zn, Cu, and Pb). These seams are hosted by Jurassic and Cretaceous sedimentary rock formation. The intrusion of igneous rocks in these formations originated metallic deposits of metasomatic and skarn types. The Raura mine is composed of polymetallic deposit of veins and replacement orebodies. The main sedimentary unit in the area is Cretaceous Machay Limestone. The Raura depression contains several orebodies each with different mineralization: predominantly Pb-Zn bearing Catuvo orebody; Ag-rich galena-bearing Lake Ninacocha orebody; Cu-Ag bearing Esperanza and Restauradora orebody. Huaron is a hydrothermal polymetallic deposit of silver, lead, zinc, and copper mineralization hosted within structures likely related to the intrusion of monzonite dikes, principally located within the Huaron anticline. Mineralization is encountered in veins parallel to the main fault systems, in replacement bodies known as "mantos" associated with the calcareous sections of the conglomerates and other favourable stratigraphic horizons, and as dissemination in the monzonitic intrusions at vein intersections.

• 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.