Metallogenesis and hydrothermal evolution of the Saibo copper deposit in the western Tianshan: evidence from fluid inclusions, H-O-S isotopes, and Re-Os geochronology

被引:5
作者
Zhang, Bowen [1 ,2 ]
Tang, Xiaofei [1 ,2 ]
Chen, Chuan [1 ,2 ]
Gong, Xiaoping [1 ,2 ]
Su, Chunmei [1 ,2 ]
机构
[1] Xinjiang Univ, Inst Geol & Mines Engn, 666 Shengli Rd, Urumqi 830047, Xinjiang, Peoples R China
[2] Xinjiang Univ, Xinjiang Key Lab Geodynam Proc & Metallogen Progn, Urumqi 830047, Xinjiang, Peoples R China
关键词
C-H-O isotope; fluid inclusions; Re-Os dating; Saibo copper deposit; West Tianshan; PORPHYRY MO DEPOSIT; STABLE-ISOTOPE; SKARN DEPOSIT; GEOCHEMISTRY; CARBON; OXYGEN; MINERALIZATION; MECHANISMS; HYDROGEN; GENESIS;
D O I
10.1007/s12303-022-0017-y
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
The Saibo copper polymetallic deposit, located in the West Tianshan Sailimu-Sitaihaiquan copper lead and zinc ore belt, is a new breakthrough in medium-large copper mine. Through the thin section authentication and the thermometric analysis of fluid inclusion, it is concluded that skarnization was developed in this deposit, the mineralization stage can be divided into retrograde skarn stage (S-1), quartz-sulfide stage (S-2) and quartz-carbonate stage (S-3). Fluid inclusions (FIs) were distinguished as liquid-rich aqueous FIs (LV-type), vapor-rich aqueous FIs (VL-type), and NaCl daughter mineral-bearing three phase FIs (S-type). The mineralization fluids indicate that the initial stage (S-1 stage) is of high temperature and high salinity, with a handful of metallic matters. During the main metallogenic stage (S-2 stage), the meteoric water is mixed, the temperature and salinity gradually decrease, the fluid is distinctly boiling, and a large amount of metallic matters are precipitated, and then to the S-3 stage, when the temperature and salinity decrease along with the carbonation. Chalcopyrite Re-Os dating yielded a mineralization age of 379.2 +/- 7.7 Ma, which corresponds well with the zircon U-Pb age (385.9 +/- 1.3 Ma) of the granite porphyry. The C-H-O isotopes indicate that the ore-forming fluid was dominated by initial mixed magmatic water in the early stage and by meteoric water in the late stage, and C is derived from limestone strata metasomatized by magmatic fluids. The S and Pb isotopes indicate that the ore-forming materials are derived from the mixed crust-mantle source, of which S is almost entirely derived from the mantle, while Pb is mainly derived from the crustal material of the orogenic belt. On the whole, the Saibo copper deposit is a typical calcium skarn type deposit, which formed in the shallower setting at active continental margin in the Late Devonian period.
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页码:45 / 65
页数:21
相关论文
共 82 条
[1]  
[薛春纪 Xue Chunji], 2014, [地学前缘, Earth Science Frontiers], V21, P128
[2]   Paleozoic Tian-Shan as a transitional region between the Rheic and Urals-Turkestan oceans [J].
Biske, Yu. S. ;
Seltmann, R. .
GONDWANA RESEARCH, 2010, 17 (2-3) :602-613
[3]   THE CANTUNG E ZONE SCHEELITE SKARN OREBODY, TUNGSTEN, NORTHWEST TERRITORIES - OXYGEN, HYDROGEN, AND CARBON ISOTOPE STUDIES [J].
BOWMAN, JR ;
COVERT, JJ ;
CLARK, AH ;
MATHIESON, GA .
ECONOMIC GEOLOGY, 1985, 80 (07) :1872-1895
[4]   Iron transport and deposition mechanisms in the Taochong iron-rich skarn deposit, Middle-Lower Yangtze Valley, Eastern China [J].
Cao, Yi ;
Du, Yangsong ;
Pang, Zhenshan ;
Gao, Fuping ;
Du, Yilun ;
Liu, Xiaoming .
ORE GEOLOGY REVIEWS, 2016, 72 :1037-1052
[5]  
Chen B., 2011, THESIS CHANGAN U XIA, DOI 10.7666/d.y1948523
[6]  
Chen YJ, 2007, ACTA PETROL SIN, V23, P2085
[7]  
Cheng ZY., 2014, GEOLOGY GEOCHEMISTRY
[8]   OXYGEN ISOTOPE-EXCHANGE BETWEEN QUARTZ AND WATER [J].
CLAYTON, RN ;
MAYEDA, TK ;
ONEIL, JR .
JOURNAL OF GEOPHYSICAL RESEARCH, 1972, 77 (17) :3057-+
[9]  
[董玉翠 Dong Yucui], 2013, [高校地质学报, Geological Journal of China Universities], V19, P245
[10]   The system H2O-NaCl.: Part I:: Correlation formulae for phase relations in temperature-pressure-composition space from 0 to 1000 °C, 0 to 5000 bar, and 0 to 1 XNaCl [J].
Driesner, Thomas ;
Heinrich, Christoph A. .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2007, 71 (20) :4880-4901