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Photographs and photomicrographs of representative hydrothermal alteration features in the Fukeshan Cu (Mo) deposit. (A) Pervasive potassic alteration assemblages are mainly composed of secondary K-feldspar and biotite. (B) Intensive silicic alteration, associated with dense disseminated chalcopyrite. (C) Silicic alteration in the granodiorite. (D) Potassic alteration locally overprinted by chlorite alteration in the granodiorite. (E) Pervasive illite/sericite replaced feldspars and mafic minerals, showing a yellow-green color. (F) Phyllic alteration in the granodiorite, with sericite replace feldspar. Abbreviations: Qz, quartz; Kfs, K-feldspar; Bt, Biotite; Chl, Chlorite; Ser, sericite; and Ccp, chalcopyrite.

Photographs and photomicrographs of representative hydrothermal alteration features in the Fukeshan Cu (Mo) deposit. (A) Pervasive potassic alteration assemblages are mainly composed of secondary K-feldspar and biotite. (B) Intensive silicic alteration, associated with dense disseminated chalcopyrite. (C) Silicic alteration in the granodiorite. (D) Potassic alteration locally overprinted by chlorite alteration in the granodiorite. (E) Pervasive illite/sericite replaced feldspars and mafic minerals, showing a yellow-green color. (F) Phyllic alteration in the granodiorite, with sericite replace feldspar. Abbreviations: Qz, quartz; Kfs, K-feldspar; Bt, Biotite; Chl, Chlorite; Ser, sericite; and Ccp, chalcopyrite.

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The Fukeshan Cu (Mo) deposit is a newfound porphyry deposit in the northern Great Xing’an Range (GXR), northeast China. In this paper, we present results of chalcopyrite Re–Os geochronology, microthermometry of the fluid inclusions (FIs), and isotopic (H–O–S–Pb) compositions of the Fukeshan Cu (Mo) deposit. Its ore-forming process can be divided in...

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... the alteration zonation is not obvious due to superposition of multiple post-metallogenic magmatism. Potassic and silicic alterations are mainly distributed in the quartz diorite porphyry and its surrounding rocks ( Figure 3A-C). Potassic alteration are characterized by the mineral assemblage of secondary K-feldspar and biotite, irregular secondary K-feldspar was intensively developed in the quartz diorite porphyry, with fuzzy boundary between the crystals ( Figure 3A). ...
Context 2
... and silicic alterations are mainly distributed in the quartz diorite porphyry and its surrounding rocks ( Figure 3A-C). Potassic alteration are characterized by the mineral assemblage of secondary K-feldspar and biotite, irregular secondary K-feldspar was intensively developed in the quartz diorite porphyry, with fuzzy boundary between the crystals ( Figure 3A). Metallic minerals that coexist with potassic and silicic alterations are mainly composed of magnetite, chalcopyrite, and minor molybdenite (Figures 3B and 4A-C). ...
Context 3
... minerals that coexist with potassic and silicic alterations are mainly composed of magnetite, chalcopyrite, and minor molybdenite (Figures 3B and 4A-C). Chlorite-illite/sericite alteration contains chlorite, illite/sericite, and minor epidote, it only locally overprints the potassic and silicic alteration ( Figure 3D,E). The main Cu mineralization is closely associated with potassic, silicic, and chlorite-illite/sericite alterations. ...
Context 4
... alteration overprints the preexisting potassic, silicic, and chlorite-illite/sericite alterations. Sericite can completely/partially replace feldspars ( Figure 3F). Minor veined and disseminated Cu (Mo) mineralization develop in the phyllic alteration zone. ...

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Citations

... 148 Ma; [2]), the Fukeshan Cu (Mo) (ca. 149 Ma; [3,4]), and the Xiaokele Cu (Mo) (ca. 150 Ma; [5]) deposits. ...
... The δ 34 S V-CDT values (0.2‰ to 3.7‰) of the seven sulfides from the Huoluotai Cu (Mo) deposit overlap those of typical porphyry deposits in the NGXR, such as the Badaguan (-2.4‰ to 3.5‰; [45]), the Chalukou (-1.9‰ to 3.6‰; [43]), the Xiaokele (-1.2‰ to 2.4‰; [5]), and the Fukeshan (-2.3‰ to 3.4‰; [4]) deposits ( Figure 10). These values are also consistent with the δ 34 S V-CDT values of typical porphyry deposits elsewhere in the world (−5‰ to 5‰; [39]). ...
... Previous studies have shown that the relatively depleted isotopic values of fluids could have been caused by water-rock interactions or magma degassing [57,58]. The depleted δ 18 O H 2 O and δD isotopic characteristics were extensively recorded by fluids from an early stage in porphyry deposits of the NGXR [59], such as the Xiaokele Cu (Mo) (-1.2‰ to 2.4‰; [5]), the Fukeshan Cu (Mo) (-2.3‰ to 3.4‰; [4]), and the Chalukou Mo (-1.9‰ to 3.6‰; [43]) deposits, which were interpreted to be predominantly of magmatic origin. The δD and δ 18 O H 2 O values for stages II, III, and IV were relatively lower than those for stage I and plotted in the region between the meteoric water line and the magmatic water field (close to the magmatic water field) (Figure 8), suggesting the involvement of some meteoric water but still dominated by magmatic water. ...
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... Moreover, the mixing of magmatic water with meteoric water occurred during stage III (as discussed in Section 7.2.3). Incursions of cooler meteoric water into the magmatic fluids may have also assisted in the temperature decrease and further promoted Cu precipitation ( Fig. 15C; Hezarkhani et al., 1999;Sun et al., 2020a). ...
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... Yong-gang Sun, Bi-le Li, Zhong-hai Zhao et al. Geoscience Frontiers 13 (2022) 101344 The Great Xing'an Range (GXR) is an important polymetallic mineralization belt in China Chen et al., 2017), and is characterized by a number of epithermal and orogenic Au, porphyry, hydrothermal vein Ag-Pb-Zn, and skarn deposits (Sun et al., 2020). Some latest Jurassic porphyry deposits are located in the northern segment of the Great Xing'an Range (NSGXR; Fig. 1C), including the Daheishan Mo (147 Hu et al., 2014), Chalukou Mo (148 Liu et al., 2014), Xiaokelehe Cu-(Mo) (150 Deng et al., 2019a), and Fukeshan Cu-(Mo) (148.7 Deng et al., 2019b) deposits, from southeast to northwest, which form a porphyry mineralization belt (Fig. 1C). ...
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Maodeng deposit is a large-sized Mo-Bi-Sn-Cu deposit located in the Xinlinhot of Inner Mongolia in the southern segment of the Great Xing’an Range. The ore-forming elements in the deposit are found in the volcanic breccia of Lower–Middle Permian Dashizhai Formation and granite porphyry of the Alubaogeshan complex, constituting distinct regional mineralization zones such as hydrothermal vein-type of Sn-Cu orebodies in the upper parts and stockworks, veinlets and disseminated-type of Mo-Bi orebodies in the lower parts. This paper has conducted an integrated study using a comprehensive field survey, molybdenite Re-Os age, fluid inclusion, and isotopic (O, H, S, and Pb) analyses. The mineralization in the deposit can be divided into four stages, which are molybdenite-native bismuth-quartz (stage I), cassiterite-wolframite-topaz-quartz (stage II), chalcopyrite-sphalerite-galena-fluorite-sericite-quartz (stage III) and stibnite-pyrite-quartz-fluorite (stage IV). The Re-Os isochron age of four molybdenite samples was estimated as 139.2 ± 3.9 Ma, indicating the deposit was formed during the Early Cretaceous. The Maodeng deposit is characterized by three kinds of fluid inclusions (FIs): liquid-rich two-phase, vapor-rich two-phase, and daughter mineral-bearing three-phase FIs. The homogenization temperatures for the FIs of stages I through IV are 292–387 °C, 222–333 °C, 172–252 °C, and 122–197 °C, with calculated salinities of 4.2–43.6 wt%, 2.1–38.9 wt%, 1.9–33.6 wt% and 0.7–5.1 wt% NaCl equiv., respectively, showing the gradual reduction in temperature and salinity of hydrothermal fluids. Hydrogen and oxygen isotopic data of quartz indicate that the dominant origin of the ore-forming solutions from deep granitic intrusions followed by their dilution by limited meteoric water. The sulfides have δ³⁴S values ranging from − 6 ‰ to − 0.49 ‰, and have ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios similar to those of K-feldspars from the Alubaogeshan pluton, suggesting the primary origin of ore-forming materials of the Maodeng deposit are magmatic. Molybdenite and native bismuth may precipitate primarily by fluid boiling, chalcopyrite could deposit mainly by fluid mixing, and cassiterite precipitate mainly through fluid boiling and mixing.
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