• Journal of Soil and Groundwater Environment
• /
• v.8 no.2
• /
• pp.9-18
• /
• 2003

Sampling of waters from each stage of treatment system (Successive Alkalinity Producing System; SAPS), tailings seepage, and spring near the Hanchang coal mine of Kangwon Province were carried out seasonally and analyzed to evaluate the source and possible path of groundwater contamination by acid mine drainage (AM). Sulfur isotope compositions were measured to identify the origin of groundwater contaminations and the sulfate reduction processes in the SAPS. Low pH and high metal concentration of spring water indicates possibility of the groundwater contamination by AMD. Removal efficiency of acidity of the SAPS was 18.17 g/$\textrm{m}^2$/day on an average and the metal removal efficiency was almost 100%, which was higher than those of other treatment systems. However, no appreciable decrease of sulfur content and almost similar sulfur isotope compositions of water from each stage of the treatment system may suggest incomplete or very poor sulfate reduction by sulfate reducing bacteria. Chemical and sulfur isotope compositions showed that spring water was contaminated by seepage from mine tailings. And seepage of stonewall, a part of treatment system was affected by both tailings seepage and mine adit drainage. In this study site, the treatment system was constructed for the only AMD from mine adit not for tailings seepages, which resulted in the groundwater contamination from tailing seepages. Similar situation is expected in other abandoned coal mine areas.

• Proceedings of the KSEEG Conference
• /
• 2007.04a
• /
• pp.459-459
• /
• 2007

See Full Text

• Economic and Environmental Geology
• /
• v.32 no.3
• /
• pp.237-245
• /
• 1999

The Mujeong au-Ag hydrothermal vein type deposits occur within the Teriary igneous rocks of the Janggi basin. Ore minerals consist of pyrite, pyrrhotite, sphalertite, chalcopyrite, galena, cosalite, lillianite, argentite and electrum, and associated with epidotization, sericitization and pyritization. Fluid inclusion studies reveal that ore fluids were low saline with a simple NaCl-$H_{2}O$ system. Fluid inclusion data indicate that homogenization temperatures and salinities of fluid are 150 to $340^{\circ}C$ and 1.0 to 6.5wt.% NaCl equivalent, respectively. Sulfur isotope compositions of sulfied minerals ( ${\delta}^{34}S$=6.2 to 9.6$\textperthousand$) indicate that the ${\delta}^{34}S_{H2S}$ value of ore fluids was about 10.4$\textperthousand$. This ${\delta}^{34}S_{H2S}$ value is likely consistent with and hydrothermal sulfur, whereas the fluids were highly influenced by mixing with meteoric water. Measured and calculated oxygen and hydrogen isotope values (${\delta}^{18}O_{H2O}$=-2.7 to 3.4 $\textperthousand$, ${\delta}D_{H2O}$ = -83.6 to -52.7 $\textperthousand$) of ore forming fluids suggest mixing with hydrothermal and meteoric water. Equilibrium thermodynamic interpretation by mineral assemblages and chemistry indicates that sulfur fugacities (-log $fs_2$) ore forming fluids range from 9.0 to 12.6 atm stage II.

• Economic and Environmental Geology
• /
• v.25 no.3
• /
• pp.297-316
• /
• 1992

The Daebong gold-silver deposits is located in 8 km southwest of Cheongyang, Chungcheongnam-Do, Republic of Korea. The gold-silver-bearing hydrothermal quartz veins was formed within the Precambrian metasediments of Gyeonggi massif. Ore minerals occur as mainly of pyrite, sphalerite (0.78~6.19 wt.% Cd), galena, pyrrhotite and minor amounts of chalcopyrite, arsenopyrite, magnetite, ilmenite, chalcocite, electrum (55.00~89.55 wt.% Au) and argentite. The gangue minerals are quartz, calcite, chlorite, K-feldspar, biotite. Wall-rock alterations such as chloritization, silicification, pyritization, carbonatization and sericitization can be observed near the quartz veins. According to the mineral paragenetic sequence based on vein structure and mineral assemblages, three stage mineralizations can be recognized. Fluid inclusion, sulfur isotope and thermodynamic data show that the ore minerals were dominantly deposited at the between 388 and $204^{\circ}C$ from fluids with salinities of 8.1~0.3 wt.% equivalent NaCl, and sulfur isotope value 4.84 to 6.40 per mil of sulfides indicates igneous sources of sulfur in the hydrothermal system and fluid inclusion salinity data suggest that thermal fluids may have magmatic origin with some degree mixing of meteoric water.

• Journal of Plant Biology
• /
• v.8 no.3
• /
• pp.1-3
• /
• 1965

The sulfur-incorporation into amino acids in germinating Soy Bean seeds was studied with the aid of Sulfate-S35. Water imbibition and isotope absorption were almostly pararelled. On the radioautogram $S^35$ was detected in cysteic acids at 90 minutes. Cysteine, cystine and cysteic acid were appeared with radioactivity at 240 minutes after the infiltration of sulfate-$S^35$. Methione was not detected on the radioautogram in the range of 300 minutes. The radioactivity of $S^35$ was detected highly in free amino acids than hydrolyzates.

• Journal of Plant Biology
• /
• v.8 no.1_2
• /
• pp.5-10
• /
• 1965

The effect of radioactive sulfur-35 on the growth and tissue respiration in rye, Secale cereale L., seedlings were studied in this investigation. The growth and respiration rate of the materials treated with the different intensities of radioactivity, represented by the different concentration(${\mu}c$) of radioactive sulfur were shown similar effects in treated groups as those of Gamma-ray or X-ray irradiation on plant materials. However, in the groups of ($0.1{\mu}c$ and ($0.4{\mu}c$ S35-solution, the growth and respiration rate were stimulated somewhat more clearly than in case of control. And the higher concentration groups, $1.6{\mu}c$, $6.4{\mu}c$, and $25.6{\mu}c$ were depressed of the growth and tissue respiration rate. The present data could be explained on the basis that the higher concentration treatments with the radioactive isotope did produce injury to the plant metabolism generally, but the moderate treatment would stimulate to the plant growth and tissue respiration.

• Nuclear Engineering and Technology
• /
• v.55 no.4
• /
• pp.1476-1484
• /
• 2023

Laboratory experiments and point monitoring of reservoir sediments have proven that stable sulfate reduction (SSR) can lower the concentrations of toxic metals and sulfate in acidic groundwater for a long time. Here, we hypothesize that SSR occurred during in situ leaching after uranium mining, which can impact the fate of acid groundwater in an entire region. To test this, we applied a sulfur isotope fractionation method to analyze the mechanism for natural attenuation of contaminated groundwater produced by acid in situ leaching of uranium (Xinjiang, China). The results showed that δ³⁴S increased over time after the cessation of uranium mining, and natural attenuation caused considerable, area-scale immobilization of sulfur corresponding to retention levels of 5.3%-48.3% while simultaneously decreasing the concentration of uranium. Isotopic evidence for SSR in the area, together with evidence for changes of pollutant concentrations, suggest that area-scale SSR is most likely also important at other acid mining sites for uranium, where retention of acid groundwater may be strengthened through natural attenuation. To recapitulate, the sulfur isotope fractionation method constitutes a relatively accurate tool for quantification of spatiotemporal trends for groundwater during migration and transformation resulting from acid in situ leaching of uranium in northern China.

• Economic and Environmental Geology
• /
• v.23 no.1
• /
• pp.1-9
• /
• 1990

A couple of Au-Ag-bearing epithermal quartz veins of Cretaceous(87.9Ma) in age are developed in the Cretaceous(112Ma) granodiorite batholith which was emplaced in Mesozoic Baegyari sedimentary formation. Au minerals consist mostly of electrum with a 54.2-61.9 wt% Au and are closely associated with sulfide minerals including pyrite, chalcopyrite, pyrrhotite, galena and sphalerite. Homogenization temperatures of fluid inclusions in quartz, fluorite and calcite are $196-368^{\circ}C$ (avg. $240^{\circ}C$), $74-176^{\circ}C$ (avg. $115^{\circ}C$) and $75-200^{\circ}C$ (avg. $119^{\circ}C$) respectively. Sulfur isotopic compositions( +5- +8‰) of ore sulfides indicate a deep-seated sulfur origin. Oxygen isotope compositions of different stages of quartz vary from +5.6 to +9.3‰ and calculated ${\delta}^{18}O$ values of ore fluid at $250^{\circ}C$ range from -3.2 to +0.4‰, reflecting an isotopically evolved ore fluid mixed with a $^{18}O$ depleted meteoric water under the variable mixing ratios between hydrothermal and meteoric waters. Isotopic data of calcite minerals support the above conclusions.

• Economic and Environmental Geology
• /
• v.41 no.1
• /
• pp.1-14
• /
• 2008

The Bongsang gold-silver deposit consists of quartz veins that fill along the fault Bone within Cretaceous andesitic lapilli tuff. Mineralization is occurred within fault-breccia zones and can be divided into two stages. Stage I which can be subdivided into early and late depositional stages is main ore mineralization and stage II is barren. Stage I began with deposition of wall-rock alteration minerals and base-metal sulfides, and was deposited by later native silver, Ag-bearing tetrahedrite, polybasite and base-metal sulfides such like pyrite, sphalerite, chalcopyrite and galena. Fluid inclusion data indicate that homogenization temperatures and salinities of stage I range from 137 to $336^{\circ}C$ and from 0.0 to 10.6 wt.% NaCl, respectively. It suggests that ore forming fluids were cooled and diluted with the mixing of meteoric water. Also, temperature and sulfur fugacity deduced mineral assemblages of late stage I are $<210^{\circ}C\;and\;<10^{-15.4}$ atm, respectively. Sulfur(3.4%o) isotope composition indicates that ore sulfur was mainly derived from a magmatic source as well as the host rocks. The calculated oxygen{2.9%o, 10.3%o(quartz: 7.9%o, 8.9%o, calcite: 2.9%o, 10.3%o)}, hydrogen(-75%o) and carbon(-7.0%o, -5.9%o) isotope compositions indicate that hydrothermal fluids may be meteoric origin with some degree of mixing of another meteoric water for paragenetic time.

• Economic and Environmental Geology
• /
• v.20 no.3
• /
• pp.169-177
• /
• 1987

The Manjang copper magnetite-fluorite orebodies are imbedded within the limestone beds of the Hwajonri Formation. The ore deposits are characterized by magnetite-fluorite bearing skarn orebody in the west orebody and copper sulfide veins of the central and main orebodies. This study includes fluid inclusion geothermometry, salinity analysis, stable isotope analysis, and application of phase rule to mineral associations in skarn ore. Ore minerals are closely associated with the skarn silicates such as garnet, wollastonite and epidote. Magnetite and fluorite are remarkable in the west orebody whereas chalcopyrite is dominate in the central and main orebodies where pyrite and pyrrhotite also appear as sulfide gangues. Homogenization temperature and salinity of fluid inclusions are measured ranging between $240^{\circ}C$ and $350^{\circ}C$, 6.3~12.9 wt. percent in quartz and $220^{\circ}C$ and $350^{\circ}C$, 8.5~9.9wt. percent in fluorite, respectively. This indicates that the filling temperature and salinity are higher in quartz than in fluorite with the tendency of both to be linearly decreased suggesting an attribution of meteoric water to the mineralization. $T-fo_2$ diagram in the Ca-Fe-Si system at 1 kb and $Xco_2$=0.02 shows that the mineral assemblages with decreasing temperature are andradite-hedenbergite-calcite, hedenbergite-andradite-quartz, magnetite-andradite-quartz, and magnetite-quartz-calcite, indicating that magnetite crystallizes mostly late skarn stage at lower temperature. According to the carbon and oxygen isotopic values of the host limestone and calcite in ores, the sourec of carbon might be mixture of host limestone and deep seated carbons. Sulfur isotope data imply that ore fluids be relatively homogeneous in sulfur isotopic composition, mainly derived from igneous source.