• Proceedings of the KSEEG Conference
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• 2000.04b
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• pp.258-259
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• 2000

• Economic and Environmental Geology
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• v.18 no.4
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• pp.343-355
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• 1985

Spectral reflectivity and microhardness were measured quantitatively on polished surfaces of a selection of bireflecting minerals obtained from several well known metallic deposits. Incremental errors are much higher than decremental errors and errors were found to be lowest in the spectral region close to the green wavelength ($544m{\mu}$). The characteristics of the spectral profile are significant in their control of white light color. The covellite and graphite have reflectivity profiles similar in shape for each principal direction, showing noticeable difference in magnitude between the profiles: The spectral reflectivity of covellite parallel to the extraordinary vibration is higher (R$$\simeq_-$$10%) than that parallel to the ordinary vibration and graphite shows opposite feature. Reflectivity of the enargite and famatinite cut parallel to the cleavage plane is always higher (R$$\simeq_-$$5%) than that of the section cut normal. The optical symmetry of 5 bireflecting minerals was determined by noting the variation in reflectivity at $544m{\mu}$. The data indicate that covellite is optically uniaxial positive and graphite is optically uniaxial negative. The Rm values for enargite and famatinite are clearly closer to the minimum value for the mineral ($R_1$) than to the maximum value ($R_2$) : the minerals can be recognized as optically biaxial positive. Enargite and famatinite cut parallel to cleavage have much higher hardness values (HV=> $200kg/mm^2$) than those cut normal to cleavage. Vickers indentations exhibit characteristic features for all the bireflecting mineral species studied. Broad radicle groupings of the mineral species can be made with regard to the reflectivity microhardness numbers.

• Economic and Environmental Geology
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• v.48 no.4
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• pp.273-285
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• 2015

The extensive hydrothermal deposits have been found, for the first time, on the western TA25 seamount caldera in the Tonga arc. The seafloor hydrothermal vents are active and immature, emitting the transparent fluids of which temperatures range from $150^{\circ}C$ to $242^{\circ}C$ (average=$203^{\circ}C$). The recovered hydrothermal sulfides are mainly composed of sphalerite, pyrite, marcasite, galena, chalcopyrite, covellite, tennantite, enargite and sulfates such as barite, gypsum/anhydrite. Predominant sphalerite categorize it into Zn-rich hydrothermal ore body. Zn-rich sulfide ores have minor enargite, indicating that mineralization occurred in high sulfidation environment. The proportion and FeS content of sphalerite increase from outside to inside of the hydrothermal ores, respectively. In particular, sphalerite has a great silver content (up to ~10 wt.%). Chalcopyrite is more frequently observed in mound than in the chimney, implying mineralization temperature in the mound is higher than in the chimney. Homogenization temperatures and salinities from fluid inclusions in barite at the mound range from $148^{\circ}C$ to $341^{\circ}C$ (average=$213^{\circ}C$) and 0.4 to 3.6 equiv. wt.% NaCl, respectively. Homogenization temperatures suggest that sulfides in the mound mineralized at a higher temperature (${\geq}200^{\circ}C$) than in the chimney.

• Korean Journal of Soil Science and Fertilizer
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• v.47 no.2
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• pp.113-119
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• 2014

Arsenic and its compounds which is one of the most toxic elements that can be found naturally on earth in small concentrations are used in the production of pesticides, herbicides, and insecticides. Most arsenic that cannot be mobilized easily when it is immobile is also found in conjunction with sulfur in minerals such as arsenopyrite (AsFeS), realgar, orpiment and enargite. In this investigation we observed the leaching of arsenic in soils amended with several levels of gravel size of arsenopyrite collected from a road construction site. Soil and gravel size of arsenopyrite were characterized by chemical and mineralogical analyses. Results of XRF analysis of arsenopyrite indicated that the proportion of arsenate was 0.075% (wt $wt^{-1}$) while the maximum amount of arsenic in soil samples was 251.3 mg $kg^{-1}$. Cumulative amounts of effluent collected from the bottom of the soil column for different mixing rate of the gravel were gradually increased where proportion of the gravel mixed was greater than 70% whereas the effluent was stabilized to the maximum after approximately 45 pore volumes of effluent or greater were collected. The arsenic in the effluent was recovered from the soil columns in which the proportion of arsenopyrite gravel was 60% or greater. The total amount of arsenic recovered as effluent was increased with increasing proportion of gravel in a soil, indicating that the arsenic in the effluent was closely related with gravel fraction of arsenopyrite.

• 한국정보컨버전스학회:학술대회논문집
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• 2008.06a
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• pp.99-102
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• 2008

Mineralogical studies of ore and alteration minerals have been conducted for the Hugo Dummett porphyry copper deposit. The Hugo Dummett porphyry copper gold deposit is located in the South Gobi region, Mongolia and currently being explored. This deposit divided into the Cu-rich Hugo Dummett South and the Cu-Au-rich Hugo Dummett North deposits. The Hugo Dummett deposits contain 1.08% copper(1.16 billion tonnes in total) and 0.23 g/t gold(Oyunchimeg et al., 2006). Copper-gold mineralization at these deposit are centered on a high-grade copper(typically>2.5%) and gold(0.5-2 g/t) zone of intense quartz stockwork veining. The high grade copper and gold zone is mainly within the Late Devonian quartz monzodiorite intrusions and augite basalt, also locally occurs in dacitic rocks. Intense quartz veining forms a lens up to 100 m wide hosted by augite basalt and partly by quartz monzodiorite. Although many explorations have been carried out, only a few scientific works were done in the Oyu Tolgoi mining area. Therefore the nature of copper-gold mineralization and orgin of the deposit is not fully understood. Copper-gold mineralization in the Hugo Dummett deposits occurs in dominantly quartz monzodiorite and minor augite basalt, dacitic rocks and locally biotite granodiorite. Chalcopyrite, pyrite, bornite, molybdenite, tennantite, tetrahedrite, enargite, sphalerite, chalcocite, covellite, eugenite, galena and gold occur as main ore minerals in the Hugo Dummett North and South deposits. These sulfides occur as: (1) a vague vein-like trail 1-3cm long and 2-3 mm wide, (2) minute, discontinuous cracks within quartz(micron scales), and (3) irregular blebs/spots(micron scales)and (4) disseminated within the sericite and plagioclase, commonly concentrated in the quartz. Sulfide minerals commonly display as a replacement, intergrown and minor exsolution texture in the both of the Hugo Dummet deposits.

• Economic and Environmental Geology
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• v.55 no.5
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• pp.465-475
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• 2022

The seafloor massive sulfide deposits are important mineral resources for base and precious metals, and their ore genesis and metal contents are mainly controlled by wall-rock leaching process and/or magmatic volatile input from the underlying magma chamber. However, the contribution of two different metal sources to the seafloor hydrothermal mineralization significantly varies in diverse geological settings and thus still remains controversial. In this review, mineralogical and geochemical characteristics of SMS deposits from mid-ocean ridges (MORs) and volcanic arcs were investigated to understand the contribution from different metal sources and to suggest future challenges that need to be addressed. As a result, the genetic occurrences of enargite and cubanite, galena and barite indicate the effects of magmatic input and water-rock interaction, respectively. Also, the distributional behaviors of Co, As, and Hg in pyrite and FeS content of sphalerite could be useful empirical indicators to discriminate the significant roles of different metal sources between MOR and Arc settings. To date, as most studies have focused on sulfide samples recovered from the seabed, further studies on magmatic sulfides and sulfate minerals are required to fully understand the genetic history of SMS deposits.