TY - JOUR
T1 - Stable isotope and geochronological study of the Mawchi Sn-W deposit, Myanmar
T2 - Implications for timing of mineralization and ore genesis
AU - Myint, Aung Zaw
AU - Yonezu, Kotaro
AU - Boyce, Adrian J.
AU - Selby, David
AU - Scherstén, Anders
AU - Tindell, Thomas
AU - Watanabe, Koichiro
AU - Swe, Ye Myint
N1 - Funding Information:
Sincere thanks are due to the Japan International Cooperation Agency (JICA) for the PhD scholarship for AZM and Global COE Program of Kyushu University for support for the field work. The Society of Economic Geologists Foundation is thanked for their student research grant to AZM. We would like to thank Alison McDonald and Julie Dougan from SUERC, UK for their valuable assistance during stable isotopic experiments. EPMA analysis was supported by Professor Yasuhito Osanai and Dr. Tatsuro Adachi from Kyushu University . We are deeply appreciated to two reviewers for their critical reading of manuscript and providing valuable comments. Special thanks are also due to Kayah Metal Production Co. Ltd and Ye Htut Kyaw Mining Co. Ltd for generously providing the first author an office space to work in and for providing logistical support. DS acknowledges the Total Endowment Fund .
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/4
Y1 - 2018/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85044459656&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85044459656&partnerID=8YFLogxK
U2 - 10.1016/j.oregeorev.2018.03.014
DO - 10.1016/j.oregeorev.2018.03.014
M3 - Article
AN - SCOPUS:85044459656
SN - 0169-1368
VL - 95
SP - 663
EP - 679
JO - Ore Geology Reviews
JF - Ore Geology Reviews
ER -