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The geochemical and mineralogical study of the Quiulacocha tailings impoundment has shown that the hydrological connection of the three studied mine-waste systems at Cerro de Pasco (Pyrite-rich waste-rock dump Excelsior, old tailings impoundment Quiulacocha, and the active tailings impoundment Ocroyoc) is a critical concern for effective acid mine drainage (AMD) control and mine-waste management. The Quiulacocha tailings covered 114 ha, comprising 79 Mt of tailings, which contained 50 wt.% pyrite, and are located at 4340 m altitude in a tropical puna climate with about 1025 mm/a rainfall and 988 mm/a of evaporation. The tailings were partially overlain by the Excelsior waste-rock dump, which contains about 26,400,000 m3 of waste rocks that cover 94 ha and contained 60 wt.% of pyrite, which origin from a massive pyrite-quartz replacement body. Therefore, these two mine-waste deposits had a direct hydrological connection, resulting in the export of AMD produced at Excelsior towards Quiulacocha. In the Quiulacocha impoundment there are two different types of tailings recognized, that interact with the AMD from Excelsior: 1) Zn–Pb-rich tailings and 2) Cu–As-rich tailings. During the sampling, the Zn–Pb-rich part of Quiulacocha was not producing important excesses of AMD from the oxidation zone, since the pH increased to near neutral values at 1 m depth. The underlying tailings were still able to neutralize the acidity produced in the oxidation zone through sulfide oxidation by the carbonates (mainly dolomite and siderite) contained in the Zn–Pb mineral assemblage. The main source of AMD in this mine-waste system is the Excelsior waste-rock dump. Its acid seepage infiltrates into Quiulacocha forming a Fe–Zn–Pb plume with a pH 5.5–6.1 and containing up to 7440 mg/L Fe, 627 mg/L Zn, and 1.22 mg/L Pb. The plume was detected at 10–13 m depth in the stratigraphy of Quiulacocha tailings. Additionally, the AMD seepage outcropping at the base of the Excelsior waste-rock dump was channeled on the tailings surface into the Quiulacocha pond (pH 2.3), which covered the Cu–As-rich tailings. Infiltration of this Fe(III)-rich AMD increased tailings oxidation in the southwestern part of the impoundment, and subsequently liberated arsenic by enargite oxidation. Additionally, the AMD collected in the Quiulacocha pond was pumped into the active Ocroyoc tailings impoundment, where sulfide oxidation was strongly enhanced by the input of dissolved Fe(III). Therefore, the AMD management and a hydrological separation of the different mine-waste systems could be a first step to prevent further extension of the AMD problem in order to prevent increased sulfide oxidation by Fe(III)-rich solutions. 相似文献
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Mineral zoning and gold occurrence in the Fortuna skarn mine, Nambija district, Ecuador 总被引：1，自引：0，他引：1
Agnès Markowski Jean Vallance Massimo Chiaradia Lluìs Fontboté 《Mineralium Deposita》2006,41(4):301-321
The Fortuna oxidized gold skarn deposit is located in the northern part of the Nambija gold district, southern Ecuador. It has been subdivided into four mineralized sites, covering a distance of 1 km, which are named from north to south: Cuerpo 3, Mine 1, Mine 2, and Southern Sector. Massive skarn bodies occur in K–Na metasomatized volcanic and volcaniclastic rocks of the Triassic Piuntza unit. They appear to result from selective replacement of volcaniclastic rocks. Very minor presence of bioclast relicts suggests the presence of subordinate limestone. Endoskarn type alteration with development of Na-rich plagioclase, K-feldspar, epidote, actinolite, anhedral pyroxene, and titanite affects a quartz–diorite porphyritic intrusion which crops out below the skarn bodies in Mine 2 and the Southern Sector. Endoskarn alteration in the intrusion grades into a K-feldspar ± biotite ± magnetite assemblage (K-alteration), suggesting that skarn formation is directly related to the quartz–diorite porphyritic intrusion, the latter being probably emplaced between 141 and 146 Ma. The massive skarn bodies were subdivided into a dominant brown garnet skarn, a distal green pyroxene–epidote skarn, and two quartz-rich varieties, a blue-green garnet skarn and light green pyroxene–garnet skarn, which occur as patches and small bodies within the former skarn types. The proximal massive brown garnet skarn zone is centered on two 060° trending faults in Mine 2, where the highest gold grades (5–10 g/t) were observed. It grades into a distal green pyroxene–epidote skarn zone to the North (Cuerpo 3). Granditic garnet shows iron enrichment from the proximal to the distal zone. Diopsidic pyroxene exhibits iron and manganese enrichment from proximal to distal zones. The retrograde stage is weakly developed and consists mainly of mineral phases filling centimeter-wide veins, vugs, and interstices between garnet and pyroxene grains. The main filling mineral is quartz, followed by K-feldspar, epidote, calcite, and chlorite, with minor sericite, apatite, titanite, hematite, pyrite, chalcopyrite, and gold. Metal and sulfur contents are low at Fortuna, and the highest gold grades coincide with high hematite abundance, which suggests that retrograde stage and gold deposition took place under oxidizing conditions. Fluid inclusions from pyroxene indicate precipitation from high temperature—high to moderate salinity fluids (400 to 460°C and 54- to 13-wt% eq. NaCl), which result probably from boiling of a moderately saline (∼8-wt% eq. NaCl) magmatic fluid. Later cooler (180 to 475°C) and moderate to low saline fluids (1- to 20-wt% eq. NaCl) were trapped in garnet, epidote, and quartz, and are interpreted to be responsible for gold deposition. Chlorite analysis indicates temperature of formation between 300 and 340°C in accordance with fluid inclusion data. It appears, thus, that gold was transported as chloride complexes under oxidizing conditions and was deposited at temperatures around 300°C when transport of chloride complexes as gold carriers is not efficient. 相似文献
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B.?RottierEmail author H.?Rezeau V.?Casanova K.?Kouzmanov R.?Moritz K.?Schl?glova M.?W?lle L.?Fontboté 《Contributions to Mineralogy and Petrology》2017,172(4):23
Heating of quartz crystals in order to study melt and high-temperature fluid inclusions is a common practice to constrain major physical and chemical parameters of magmatic and hydrothermal processes. Diffusion and modification of trace element content in quartz and its hosted melt inclusions have been investigated through step-heating experiments of both matrix-free quartz crystals and quartz crystals associated with sulfides and other minerals using a Linkam TS1500 stage. Magmatic and hydrothermal quartz were successively analyzed after each heating step for Cu, Al, and Ti using electron probe micro-analyzer. After the last heating step, quartz crystals and their hosted melt inclusions were analyzed by laser ablation inductively coupled plasma mass spectrometry and compared to unheated samples. Heated samples reveal modification of Cu, Li, Na, and B contents in quartz and modification of Cu, Li, Ag, and K concentrations in melt inclusions. Our results show that different mechanisms of Cu, Li, and Na incorporation occur in magmatic and hydrothermal quartz. Heated magmatic quartz records only small, up to a few ppm, enrichment in Cu and Na, mostly substituting for Li. By contrast, heated hydrothermal quartz shows enrichment up to several hundreds of ppm in Cu, Li, and Na, which substitute for originally present H. This study reveals that the composition of both quartz and its hosted melt inclusions may be significantly modified upon heating experiments, leading to erroneous quantification of elemental concentrations. In addition, each quartz crystal also becomes significantly enriched in Cu in the sub-surface layer during heating. We propose that sub-surface Cu enrichment is a direct indication of Cu diffusion in quartz externally sourced from both the surrounding sulfides as well as the copper pins belonging to the heating device. Our study shows that the chemical compositions of both heated quartz and its hosted inclusions must be interpreted with great caution to avoid misleading geological interpretations. 相似文献