| 2. |
- Myint, Aung Zaw, et al.
(författare)
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Stable isotope and geochronological study of the Mawchi Sn-W deposit, Myanmar : Implications for timing of mineralization and ore genesis
- 2018
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Ingår i: Ore Geology Reviews. - : Elsevier BV. - 0169-1368. ; 95, s. 663-679
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Tidskriftsartikel (refereegranskat)abstract
- Myanmar is endowed with abundant Sn-W mineralization, pre-eminent amongst which is the world-class Mawchi deposit. In the Mawchi area, N-S trending vertical or steeply dipping quartz veins are hosted by both Eocene granite and Carboniferous to Early Permian metasediments. Three stages of ore formation are recognized; (i) tourmaline-cassiterite stage (ii) main ore stage and (iii) sulfide stage. Tourmaline, cassiterite and pyrite-I are early-formed minerals and are representative of the first stage. Their deposition continued together with wolframite, scheelite, molybdenite, arsenopyrite, pyrite-II, fluorite and danalite, which form the second stage. This was followed by the successive deposition of sulfides such as chalcopyrite, sphalerite, galena and Pb-Bi sulfides. A 40Ar/39Ar magmatic biotite plateau age of 41.50 ± 0.16 Ma (MSWD = 2.5) is determined for the Mawchi biotite granite which we interpret as the time the granite cooled through the biotite blocking temperature, and is consistent with a previously reported LA-ICP-MS U-Pb zircon concordia age of 42.72 ± 0.94 Ma (MSWD = 2). A molybdenite Re-Os model age of 42.4 ± 1.2 Ma indicates that Sn-W mineralization was synchronous with late Eocene granitic magmatism. Our 40Ar/39Ar hydrothermal muscovite plateau ages from the tourmaline granite (40.14 ± 0.14 Ma; MSWD = 1.48) and quartz vein selvages (40.80 ± 0.12 Ma; MSWD = 0.47) define the timing of hydrothermal alteration and simultaneous veining that accompanied the late stage of ore forming at Mawchi. Fluid inclusion microthermometry from cassiterite, scheelite, quartz, and fluorite reveals that ore fluids in the cassiterite-tourmaline stage and main ore stage are characterized by moderate homogenization temperatures (Th = 260–345 °C) and salinities (4.5–15.7 wt% NaCl equiv), while the sulfide stage is characterized by lower temperatures (Th = 175–260 °C) and moderate to low salinity (2.5–13 wt% NaCl equiv). The mean δ34S of all sulfides is 2.9 ± 2.9‰ which is suggestive that the overall system is dominated by magmatic sulfur. The similarity of δ34S values in galena and Pb-Bi sulfides (−1.3 to 2.7‰) suggest that sulfur, and inference the Pb and Bi were transported by a common fluid, probably of magmatic origin. The calculated δ18OH2O of the hydrothermal fluid associated with cassiterite and tourmaline is 7.3–8.4‰. Scheelite and quartz deposition is characterized by lighter δ18OH2O values (2.1–4.9‰) indicating that the ore fluid might be mixed with another source of water, perhaps, meteoric. Hydrogen isotopic compositions (δD = −51 to −121‰) again indicate that origin of the ore fluid is magmatic, but δD (∼−120‰) is low enough to support the δ18OH2O data that suggests, in part, a meteoric water component to the hydrothermal fluids at Mawchi.
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| 3. |
- Tindell, Thomas, et al.
(författare)
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The Kago low-sulfidation gold and silver deposit : A peripheral mineralisation to the Nansatsu high-sulfidation system, southern Kyushu, Japan
- 2018
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Ingår i: Ore Geology Reviews. - : Elsevier BV. - 0169-1368. ; 102, s. 951-966
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Tidskriftsartikel (refereegranskat)abstract
- The Kago deposit is a small deposit located at the southern tip of the Satsuma Peninsula of Southern Kyushu, Japan. It lies proximal to the well-known Nansatsu-type mineralisation province dominated by high-sulfidation type epithermal deposits. The deposit was heavily mined in the 18 th Century, largely for its relatively higher gold compared to that of surrounding and regional deposits. The Kago deposit is a typical low-sulfidation deposit, characterised by adularia-quartz veins, composed of electrum, Ag-tetrahedrite, polybasite, chalcopyrite and pyrite. Based on mine records, the grade ranged from 4.1 to 13.3 g/t Au and 2.6-6.6 g/t Ag. Alteration grades from low to high temperature argillic into a propylitic zone at the extremes of the vein exposures. Carbonate is absent. Fluid inclusion microthermometry reveals a typical temperature range of 220-240 °C with salinity of 0.7-2.6 NaCl eq. wt%. Electrum from high-grade ore ranges from 66 to 69 wt% Au. 40Ar/39Ar age dating of adularia bearing colloform/crustiform and brecciated veins, suggests a mineralisation event from 4.23 to 4.0 Ma. δ18O of veined and silicified quartz ranges from +4.0 to +18.4‰. δ18OH2O of fluids in equilibrium with quartz, in the dominant range of measured fluid inclusion temperatures, ranges from -6.5‰ to -0.2‰. δ34S of pyrite has a narrow range from -1.8 to 2.7‰. The deposit lies at the northern extent of the classic Nansatsu high-sulfidation epithermal area, in which a number of silicified bodies punctuate the region in a roughly semi-circular shape. The Kago deposit lies within the principle mineralisation age range of the high-sulfidation deposits, which range from 5.5 to 3.7 Ma. The structural displacement of the Kago deposit from the Nansatsu mineralisation and the differing host rocks has greatly influenced alteration, ore and rock-water interaction of the ore depositing fluids. Here we seek to establish the relationship that this extended mineral province has between the differing styles of mineralisation.
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