Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China

The Yuku is a large porphyry Mo deposit (1.5 Mt at 0.12% Mo) in the Luanchuan ore district of the East Qinling orogen, central China. The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum miner...

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Veröffentlicht in:Geological journal (Chichester, England) England), 2021-08, Vol.56 (8), p.4380-4400
Hauptverfasser: Xue, Liwei, Wang, Gongwen, Du, Yangsong, Cao, Yi
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Cao, Yi
description The Yuku is a large porphyry Mo deposit (1.5 Mt at 0.12% Mo) in the Luanchuan ore district of the East Qinling orogen, central China. The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum mineralization is generally associated with potassic and phyllic alteration. Hydrothermal processes in the Yuku deposit are divided into four stages: (I) a quartz–K‐feldspar–biotite ± pyrite stage, (II) a quartz–molybdenite ± pyrite ± K‐feldspar ± sericite stage, (III) a quartz–polymetallic sulphide stage, and (IV) a calcite ± quartz ± fluorite ± pyrite stage. The fluid evolution during these hydrothermal stages was constrained through systematic investigation of fluid inclusions (FIs) and H−O isotopes. Four types of primary or pseudosecondary FIs were recognized in hydrothermal quartz and calcite: two‐phase liquid‐rich inclusions (L‐type), two‐phase vapour‐rich inclusions (V‐type), halite‐bearing (hypersaline) inclusions (H‐type), and three‐phase CO2‐bearing inclusions (C‐type). FIs within Stages I–IV have homogenization temperatures of 375 to >550, 297–400, 198–298, and 149–188°C, with salinities of 0.53–13.18, 0.35–40.23, 5.11–11.81, and 5.71–9.73 wt% NaCl equiv., respectively. In Stage I, coexisting vapour‐rich (V‐type) and liquid‐rich (L‐type) FIs have similar homogenization temperatures (488 to >550°C) and distinct salinities, indicating fluid boiling during the formation of quartz–K‐feldspar–biotite veins at a pressure of 550–700 bar and a lithostatic depth of 2.3–2.8 km. In Stage II, FIs in quartz were also trapped under boiling conditions, as evidenced by coexisting hypersaline H‐type (34.13–40.23 wt% NaCl equiv.) and low‐salinity V‐type (0.35–2.24 wt% NaCl equiv.) inclusions, which formed at temperatures of 309–361°C and hydrostatic depths of 1.0–2.0 km, equivalent to pressures of 100–200 bar. During Stage III, the ore‐forming fluids were cooler (198–298°C) and more dilute (5.11–11.81 wt% NaCl equiv.) due to the involvement of meteoric water, with minimum trapping pressures estimated at
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The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum mineralization is generally associated with potassic and phyllic alteration. Hydrothermal processes in the Yuku deposit are divided into four stages: (I) a quartz–K‐feldspar–biotite ± pyrite stage, (II) a quartz–molybdenite ± pyrite ± K‐feldspar ± sericite stage, (III) a quartz–polymetallic sulphide stage, and (IV) a calcite ± quartz ± fluorite ± pyrite stage. The fluid evolution during these hydrothermal stages was constrained through systematic investigation of fluid inclusions (FIs) and H−O isotopes. Four types of primary or pseudosecondary FIs were recognized in hydrothermal quartz and calcite: two‐phase liquid‐rich inclusions (L‐type), two‐phase vapour‐rich inclusions (V‐type), halite‐bearing (hypersaline) inclusions (H‐type), and three‐phase CO2‐bearing inclusions (C‐type). FIs within Stages I–IV have homogenization temperatures of 375 to &gt;550, 297–400, 198–298, and 149–188°C, with salinities of 0.53–13.18, 0.35–40.23, 5.11–11.81, and 5.71–9.73 wt% NaCl equiv., respectively. In Stage I, coexisting vapour‐rich (V‐type) and liquid‐rich (L‐type) FIs have similar homogenization temperatures (488 to &gt;550°C) and distinct salinities, indicating fluid boiling during the formation of quartz–K‐feldspar–biotite veins at a pressure of 550–700 bar and a lithostatic depth of 2.3–2.8 km. In Stage II, FIs in quartz were also trapped under boiling conditions, as evidenced by coexisting hypersaline H‐type (34.13–40.23 wt% NaCl equiv.) and low‐salinity V‐type (0.35–2.24 wt% NaCl equiv.) inclusions, which formed at temperatures of 309–361°C and hydrostatic depths of 1.0–2.0 km, equivalent to pressures of 100–200 bar. During Stage III, the ore‐forming fluids were cooler (198–298°C) and more dilute (5.11–11.81 wt% NaCl equiv.) due to the involvement of meteoric water, with minimum trapping pressures estimated at &lt;100–150 bar, corresponding to a hydrostatic depth of &lt;1.0 km. In Stage IV, temperatures decreased further to 149–188°C, with lower salinities (5.71–9.73 wt% NaCl equiv.), indicating a post‐ore fluid stage. These data suggest that the mineralizing fluids forming the Yuku Mo deposit changed from early moderate‐ to low‐salinity CO2‐rich fluids in the H2O–NaCl–CO2 system that formed at high temperature and pressure, to late H2O–NaCl low‐salinity fluids that formed at low temperature and pressure. H−O isotopic compositions indicate that the mineralizing fluids had a dominantly magmatic signature but were diluted by meteoric waters. Combining our integrated analysis of the fluid evolution and deposit geology, we propose that fluid boiling and fluid–rock interaction, including intensive potassic alteration, changed the salinity and triggered CO2 escape, leading to a decrease in fO2 and an increase in the acidity of the ore‐forming fluids, which ultimately controlled the deposition of molybdenite in the Yuku Mo deposit. Fluid evolution paths of the Yuku Mo deposit. The initial fluids exsolved from deep magma chamber are assumed supercritical magmatic fluids with an initial salinity of 6–8 wt% NaCl equiv. These fluids followed three different cooling paths: (a) path 1 shows the fluid trajectory forming quartz–K‐feldspar–biotite vein (488–550°C, 550–700 bar, and 2.3–2.8 km under a lithostatic condition); (b) path 2 shows the trajectory forming Mo‐dominated mineralization (309–361°C, 100–200 bar, and 1.0–2.0 km under a hydrostatic depth); (c) path 3 shows the trajectory forming quartz–polymetallic sulfide stage of mineralization (198–298°C, &lt;100–150 bar, and &lt;1.0 km under a hydrostatic depth).</description><identifier>ISSN: 0072-1050</identifier><identifier>EISSN: 1099-1034</identifier><identifier>DOI: 10.1002/gj.4191</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>Acidity ; Biotite ; Boiling ; Calcite ; Carbon dioxide ; Depth ; Dilution ; East Qinling ; Economics ; Evolution ; Feldspars ; Fluid inclusions ; Fluids ; Fluorite ; Geology ; Halite ; High temperature ; Homogenization ; Hydrothermal activity ; H−O isotopes ; Isotopes ; Low temperature ; Mesozoic ; Meteoric water ; Mineralization ; Molybdenite ; Molybdenum ; Orogeny ; porphyry ; Pressure ; Pyrite ; Quartz ; Salinity ; Salinity effects ; Sodium chloride ; Sulfides ; Sulphides ; Yuku Mo deposit</subject><ispartof>Geological journal (Chichester, England), 2021-08, Vol.56 (8), p.4380-4400</ispartof><rights>2021 John Wiley &amp; Sons Ltd</rights><rights>2021 John Wiley &amp; Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a3781-7c1dc5b03a73ebecc46b24e3bced996e4fafbfbb76b88c9e0f55693e529328193</citedby><cites>FETCH-LOGICAL-a3781-7c1dc5b03a73ebecc46b24e3bced996e4fafbfbb76b88c9e0f55693e529328193</cites><orcidid>0000-0002-6339-9720</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fgj.4191$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fgj.4191$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45552,45553</link.rule.ids></links><search><creatorcontrib>Xue, Liwei</creatorcontrib><creatorcontrib>Wang, Gongwen</creatorcontrib><creatorcontrib>Du, Yangsong</creatorcontrib><creatorcontrib>Cao, Yi</creatorcontrib><title>Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China</title><title>Geological journal (Chichester, England)</title><description>The Yuku is a large porphyry Mo deposit (1.5 Mt at 0.12% Mo) in the Luanchuan ore district of the East Qinling orogen, central China. The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum mineralization is generally associated with potassic and phyllic alteration. Hydrothermal processes in the Yuku deposit are divided into four stages: (I) a quartz–K‐feldspar–biotite ± pyrite stage, (II) a quartz–molybdenite ± pyrite ± K‐feldspar ± sericite stage, (III) a quartz–polymetallic sulphide stage, and (IV) a calcite ± quartz ± fluorite ± pyrite stage. The fluid evolution during these hydrothermal stages was constrained through systematic investigation of fluid inclusions (FIs) and H−O isotopes. Four types of primary or pseudosecondary FIs were recognized in hydrothermal quartz and calcite: two‐phase liquid‐rich inclusions (L‐type), two‐phase vapour‐rich inclusions (V‐type), halite‐bearing (hypersaline) inclusions (H‐type), and three‐phase CO2‐bearing inclusions (C‐type). FIs within Stages I–IV have homogenization temperatures of 375 to &gt;550, 297–400, 198–298, and 149–188°C, with salinities of 0.53–13.18, 0.35–40.23, 5.11–11.81, and 5.71–9.73 wt% NaCl equiv., respectively. In Stage I, coexisting vapour‐rich (V‐type) and liquid‐rich (L‐type) FIs have similar homogenization temperatures (488 to &gt;550°C) and distinct salinities, indicating fluid boiling during the formation of quartz–K‐feldspar–biotite veins at a pressure of 550–700 bar and a lithostatic depth of 2.3–2.8 km. In Stage II, FIs in quartz were also trapped under boiling conditions, as evidenced by coexisting hypersaline H‐type (34.13–40.23 wt% NaCl equiv.) and low‐salinity V‐type (0.35–2.24 wt% NaCl equiv.) inclusions, which formed at temperatures of 309–361°C and hydrostatic depths of 1.0–2.0 km, equivalent to pressures of 100–200 bar. During Stage III, the ore‐forming fluids were cooler (198–298°C) and more dilute (5.11–11.81 wt% NaCl equiv.) due to the involvement of meteoric water, with minimum trapping pressures estimated at &lt;100–150 bar, corresponding to a hydrostatic depth of &lt;1.0 km. In Stage IV, temperatures decreased further to 149–188°C, with lower salinities (5.71–9.73 wt% NaCl equiv.), indicating a post‐ore fluid stage. These data suggest that the mineralizing fluids forming the Yuku Mo deposit changed from early moderate‐ to low‐salinity CO2‐rich fluids in the H2O–NaCl–CO2 system that formed at high temperature and pressure, to late H2O–NaCl low‐salinity fluids that formed at low temperature and pressure. H−O isotopic compositions indicate that the mineralizing fluids had a dominantly magmatic signature but were diluted by meteoric waters. Combining our integrated analysis of the fluid evolution and deposit geology, we propose that fluid boiling and fluid–rock interaction, including intensive potassic alteration, changed the salinity and triggered CO2 escape, leading to a decrease in fO2 and an increase in the acidity of the ore‐forming fluids, which ultimately controlled the deposition of molybdenite in the Yuku Mo deposit. Fluid evolution paths of the Yuku Mo deposit. The initial fluids exsolved from deep magma chamber are assumed supercritical magmatic fluids with an initial salinity of 6–8 wt% NaCl equiv. These fluids followed three different cooling paths: (a) path 1 shows the fluid trajectory forming quartz–K‐feldspar–biotite vein (488–550°C, 550–700 bar, and 2.3–2.8 km under a lithostatic condition); (b) path 2 shows the trajectory forming Mo‐dominated mineralization (309–361°C, 100–200 bar, and 1.0–2.0 km under a hydrostatic depth); (c) path 3 shows the trajectory forming quartz–polymetallic sulfide stage of mineralization (198–298°C, &lt;100–150 bar, and &lt;1.0 km under a hydrostatic depth).</description><subject>Acidity</subject><subject>Biotite</subject><subject>Boiling</subject><subject>Calcite</subject><subject>Carbon dioxide</subject><subject>Depth</subject><subject>Dilution</subject><subject>East Qinling</subject><subject>Economics</subject><subject>Evolution</subject><subject>Feldspars</subject><subject>Fluid inclusions</subject><subject>Fluids</subject><subject>Fluorite</subject><subject>Geology</subject><subject>Halite</subject><subject>High temperature</subject><subject>Homogenization</subject><subject>Hydrothermal activity</subject><subject>H−O isotopes</subject><subject>Isotopes</subject><subject>Low temperature</subject><subject>Mesozoic</subject><subject>Meteoric water</subject><subject>Mineralization</subject><subject>Molybdenite</subject><subject>Molybdenum</subject><subject>Orogeny</subject><subject>porphyry</subject><subject>Pressure</subject><subject>Pyrite</subject><subject>Quartz</subject><subject>Salinity</subject><subject>Salinity effects</subject><subject>Sodium chloride</subject><subject>Sulfides</subject><subject>Sulphides</subject><subject>Yuku Mo deposit</subject><issn>0072-1050</issn><issn>1099-1034</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp10E9LwzAYBvAgCs4pfoWABw-uM2n6ZznKmFOZiKCIp5C0b7rUmtSkVfrtrc6rp-c5_HhfeBA6pWROCYkvq3qeUE730IQSziNKWLKPJoTk8dhTcoiOQqgJoZQkdIJe1mAhmIClLbFuelNi-HRN3xlnsdO42wJ-7d963Drfbgc_4HuHS2hdMN0Mr2To8KOxjbEVdt5VYGd4uTVWHqMDLZsAJ385Rc_Xq6flTbR5WN8urzaRZPmCRnlByyJVhMmcgYKiSDIVJ8BUASXnGSRaaqWVyjO1WBQciE7TjDNIY87iBeVsis52d1vvPnoInahd7-34UsRpmmeMM5aM6nynCu9C8KBF68279IOgRPysJqpa_Kw2youd_DINDP8xsb771d8NpWyU</recordid><startdate>202108</startdate><enddate>202108</enddate><creator>Xue, Liwei</creator><creator>Wang, Gongwen</creator><creator>Du, Yangsong</creator><creator>Cao, Yi</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H96</scope><scope>L.G</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-6339-9720</orcidid></search><sort><creationdate>202108</creationdate><title>Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China</title><author>Xue, Liwei ; Wang, Gongwen ; Du, Yangsong ; Cao, Yi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a3781-7c1dc5b03a73ebecc46b24e3bced996e4fafbfbb76b88c9e0f55693e529328193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acidity</topic><topic>Biotite</topic><topic>Boiling</topic><topic>Calcite</topic><topic>Carbon dioxide</topic><topic>Depth</topic><topic>Dilution</topic><topic>East Qinling</topic><topic>Economics</topic><topic>Evolution</topic><topic>Feldspars</topic><topic>Fluid inclusions</topic><topic>Fluids</topic><topic>Fluorite</topic><topic>Geology</topic><topic>Halite</topic><topic>High temperature</topic><topic>Homogenization</topic><topic>Hydrothermal activity</topic><topic>H−O isotopes</topic><topic>Isotopes</topic><topic>Low temperature</topic><topic>Mesozoic</topic><topic>Meteoric water</topic><topic>Mineralization</topic><topic>Molybdenite</topic><topic>Molybdenum</topic><topic>Orogeny</topic><topic>porphyry</topic><topic>Pressure</topic><topic>Pyrite</topic><topic>Quartz</topic><topic>Salinity</topic><topic>Salinity effects</topic><topic>Sodium chloride</topic><topic>Sulfides</topic><topic>Sulphides</topic><topic>Yuku Mo deposit</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xue, Liwei</creatorcontrib><creatorcontrib>Wang, Gongwen</creatorcontrib><creatorcontrib>Du, Yangsong</creatorcontrib><creatorcontrib>Cao, Yi</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) 2: Ocean Technology, Policy &amp; Non-Living Resources</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Environment Abstracts</collection><jtitle>Geological journal (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xue, Liwei</au><au>Wang, Gongwen</au><au>Du, Yangsong</au><au>Cao, Yi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China</atitle><jtitle>Geological journal (Chichester, England)</jtitle><date>2021-08</date><risdate>2021</risdate><volume>56</volume><issue>8</issue><spage>4380</spage><epage>4400</epage><pages>4380-4400</pages><issn>0072-1050</issn><eissn>1099-1034</eissn><abstract>The Yuku is a large porphyry Mo deposit (1.5 Mt at 0.12% Mo) in the Luanchuan ore district of the East Qinling orogen, central China. The economic Mo ore bodies occur as veins, veinlets, and disseminated ore and are developed mainly within the late Mesozoic Yuku porphyritic granite. Molybdenum mineralization is generally associated with potassic and phyllic alteration. Hydrothermal processes in the Yuku deposit are divided into four stages: (I) a quartz–K‐feldspar–biotite ± pyrite stage, (II) a quartz–molybdenite ± pyrite ± K‐feldspar ± sericite stage, (III) a quartz–polymetallic sulphide stage, and (IV) a calcite ± quartz ± fluorite ± pyrite stage. The fluid evolution during these hydrothermal stages was constrained through systematic investigation of fluid inclusions (FIs) and H−O isotopes. Four types of primary or pseudosecondary FIs were recognized in hydrothermal quartz and calcite: two‐phase liquid‐rich inclusions (L‐type), two‐phase vapour‐rich inclusions (V‐type), halite‐bearing (hypersaline) inclusions (H‐type), and three‐phase CO2‐bearing inclusions (C‐type). FIs within Stages I–IV have homogenization temperatures of 375 to &gt;550, 297–400, 198–298, and 149–188°C, with salinities of 0.53–13.18, 0.35–40.23, 5.11–11.81, and 5.71–9.73 wt% NaCl equiv., respectively. In Stage I, coexisting vapour‐rich (V‐type) and liquid‐rich (L‐type) FIs have similar homogenization temperatures (488 to &gt;550°C) and distinct salinities, indicating fluid boiling during the formation of quartz–K‐feldspar–biotite veins at a pressure of 550–700 bar and a lithostatic depth of 2.3–2.8 km. In Stage II, FIs in quartz were also trapped under boiling conditions, as evidenced by coexisting hypersaline H‐type (34.13–40.23 wt% NaCl equiv.) and low‐salinity V‐type (0.35–2.24 wt% NaCl equiv.) inclusions, which formed at temperatures of 309–361°C and hydrostatic depths of 1.0–2.0 km, equivalent to pressures of 100–200 bar. During Stage III, the ore‐forming fluids were cooler (198–298°C) and more dilute (5.11–11.81 wt% NaCl equiv.) due to the involvement of meteoric water, with minimum trapping pressures estimated at &lt;100–150 bar, corresponding to a hydrostatic depth of &lt;1.0 km. In Stage IV, temperatures decreased further to 149–188°C, with lower salinities (5.71–9.73 wt% NaCl equiv.), indicating a post‐ore fluid stage. These data suggest that the mineralizing fluids forming the Yuku Mo deposit changed from early moderate‐ to low‐salinity CO2‐rich fluids in the H2O–NaCl–CO2 system that formed at high temperature and pressure, to late H2O–NaCl low‐salinity fluids that formed at low temperature and pressure. H−O isotopic compositions indicate that the mineralizing fluids had a dominantly magmatic signature but were diluted by meteoric waters. Combining our integrated analysis of the fluid evolution and deposit geology, we propose that fluid boiling and fluid–rock interaction, including intensive potassic alteration, changed the salinity and triggered CO2 escape, leading to a decrease in fO2 and an increase in the acidity of the ore‐forming fluids, which ultimately controlled the deposition of molybdenite in the Yuku Mo deposit. Fluid evolution paths of the Yuku Mo deposit. The initial fluids exsolved from deep magma chamber are assumed supercritical magmatic fluids with an initial salinity of 6–8 wt% NaCl equiv. These fluids followed three different cooling paths: (a) path 1 shows the fluid trajectory forming quartz–K‐feldspar–biotite vein (488–550°C, 550–700 bar, and 2.3–2.8 km under a lithostatic condition); (b) path 2 shows the trajectory forming Mo‐dominated mineralization (309–361°C, 100–200 bar, and 1.0–2.0 km under a hydrostatic depth); (c) path 3 shows the trajectory forming quartz–polymetallic sulfide stage of mineralization (198–298°C, &lt;100–150 bar, and &lt;1.0 km under a hydrostatic depth).</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/gj.4191</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-6339-9720</orcidid></addata></record>
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subjects Acidity
Biotite
Boiling
Calcite
Carbon dioxide
Depth
Dilution
East Qinling
Economics
Evolution
Feldspars
Fluid inclusions
Fluids
Fluorite
Geology
Halite
High temperature
Homogenization
Hydrothermal activity
H−O isotopes
Isotopes
Low temperature
Mesozoic
Meteoric water
Mineralization
Molybdenite
Molybdenum
Orogeny
porphyry
Pressure
Pyrite
Quartz
Salinity
Salinity effects
Sodium chloride
Sulfides
Sulphides
Yuku Mo deposit
title Genesis and fluid evolution of the Yuku porphyry Mo deposit, East Qinling orogen, China
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