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Guo, D.; Li, Y.; Duan, C.; Fan, C.; Sun, P. Porphyry Mo Deposits. Encyclopedia. Available online: https://encyclopedia.pub/entry/47315 (accessed on 15 November 2024).
Guo D, Li Y, Duan C, Fan C, Sun P. Porphyry Mo Deposits. Encyclopedia. Available at: https://encyclopedia.pub/entry/47315. Accessed November 15, 2024.
Guo, Dongwei, Yanhe Li, Chao Duan, Changfu Fan, Pengcheng Sun. "Porphyry Mo Deposits" Encyclopedia, https://encyclopedia.pub/entry/47315 (accessed November 15, 2024).
Guo, D., Li, Y., Duan, C., Fan, C., & Sun, P. (2023, July 26). Porphyry Mo Deposits. In Encyclopedia. https://encyclopedia.pub/entry/47315
Guo, Dongwei, et al. "Porphyry Mo Deposits." Encyclopedia. Web. 26 July, 2023.
Porphyry Mo Deposits
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Porphyry Mo deposits are the most important type of Mo resource. They result from a high oxygen fugacity of the parent magma, which acts as an effective indicator for evaluating the mineralization. In the ore-forming system of porphyry Mo deposits, sulfur exists mainly as sulfate in highly oxidized magma but as sulfide in ores. What triggers the reduction in the mineralization system that leads to sulfide precipitation has not yet been determined. 

porphyry Mo deposits high oxygen fugacity redox state transformation

1. Introduction

Porphyry Mo deposits are an important source of Mo resources. The distribution of Mo resources is uneven globally, with approximately 90% of molybdenum distributed in China, America, Peru, Chile, and Canada [1]. The formation of porphyry molybdenum deposits is closely related to the subduction of the oceanic crust [2]. They have been classified as Climax-type (rift-related, represented by the deposits in the Climax-Henderson Mo belt in America) [3][4][5], Endako-type (arc-related, represented by the Endako and MAX deposits in Canada; Quartz Hill, Thompson Creek, and Buckingham deposits in America; Tamboras deposit in Peru; and deposits in the Gangdese metallogenic belt and the Central Asian orogenic belt in China) [6][7][8][9][10][11][12][13][14][15][16][17][18], and Dabie-type (collision-related, typified by deposits in the Qingling-Dabie Mo belt in China) deposits [19][20][21][22][23].
The parent magma of porphyry Mo deposits often contains primitive gypsum, magnetite/hematite, and other highly oxidized minerals, implying a very high oxygen fugacity of the primitive magma [3][4][24][25][26][27][28][29][30][31]. The high oxygen fugacity of the initial magma is favorable for chalcophile ore metal elements such as Cu and Mo to enter the magma as incompatible components during partial melting, forming sulfur-rich and Mo-rich ore-forming magma. Furthermore, the high oxygen fugacity makes the sulfur present mainly as sulfate anions, which prevents ore-forming metal elements from precipitating as sulfide in the magma during the migration and evolution of magma [32][33][34]. Therefore, a high oxygen fugacity has become a widely accepted criterion for distinguishing mineralized and nonmineralized porphyries [34][35][36][37][38][39][40][41][42][43][44]. A high fractionation and oxygen fugacity of the parent magma and enrichment of Mo, S, and H2O are favorable conditions for porphyry Mo ore production [45]. However, in some deposits, melts and fluids in mineralization systems have lower Mo contents (2–25 ppm) [30][46][47][48], indicating conditions for the accumulation and efficient unloading of ore-forming materials, which may be more important than the initial Mo concentration of magma [49].
Sulfur exists mainly as sulfate anions in the highly oxidized magma but also as sulfide in ores, indicating significant changes in redox conditions during mineralization. This variation is an essential scientific issue related to the genesis and efficient evaluation of porphyry Mo deposits. However, there is no specific interpretation yet. Li and his coauthors proposed that highly oxidized porphyry with reductive carbonaceous surrounding rocks or Fe-rich volcanic rocks was a new indicator for efficiently evaluating porphyry mineralization [42]. There are two primary reductive surrounding rocks related to porphyry mineralization: carbonaceous surrounding rocks and Fe-rich volcanic rocks [42]. Carbonaceous surrounding rocks are more developed in porphyry Mo deposits in China [22][50][51][52][53][54][55], and Fe-rich volcanic rocks are prevalent in porphyry Mo deposits in South America [56][57][58][59].

2. Geological Characteristics of Porphyry Mo Deposits and Their Relationship with Carbonaceous Surrounding Rocks

Numerous studies have demonstrated that dark-black reductive carbonaceous sedimentary layers are widely developed in the roof and surrounding rocks of giant or large porphyry Mo deposits, such as the Shuidigou Formation of the Proterozoic Taihua Supergroup and the Xianrenchong Formation of the Proterozoic Luzhenguan Group, which contains graphitic schist and graphite gneiss; the Baishugou, Sanchuan, Nannihu and Meiyaogou Formations of the Neoproterozoic Luanchuan Group, which contains carbonaceous slate and shale developed in the East Qinglin-Dabie Mo mineralization belt (Figure 1) [22][50][51][52][53][54][55][60][61]; and the Cretaceous Mancos Formation and Mesaverde Group, which contains coal and carbonaceous shale and siltstone that are widely distributed in the Climax-Henderson Mo mineralization belt in North America [25][62][63][64][65][66][67]. Carbonaceous sedimentary layers provide reductive agents for the porphyry mineralization system and serve as an ideal natural water-resisting layer, critical factors, and conditions for forming high-grade porphyry Mo ores. The CH4, produced by organic matter pyrolysis or carbonaceous interaction with hydrothermal fluids, triggers a sulfate reduction in highly oxidizing mineralization solutions and subsequent efficient ore precipitation. To further understand the role of carbonaceous surrounding rocks in porphyry mineralization, researchers chose several typical Mo deposits in East Qinling-Dabie and Climax-Henderson, which are the world’s two most extensive Mo mineralization belts, as shown below in Figure 1.
Figure 1. Carbonaceous surrounding rocks are closely related to Mo mineralization in the East Qinling-Dabie Mo mineralization belt. (A) The surface exposure of the Sanhe graphite deposit occurred in the Xianrenchong Formation of the Luzhenguan Group in the periphery of the Shapinggou Mo deposit in Jinzhai. (B) Rock cores from the Sanhe graphite deposit in Xingfu village. (C) The thick-layered black carbonaceous slate of the Baishugou Formation within the boundary of the Nannihu-Sandaozhuang Mo deposits. (D) Black carbonaceous slate and shale of the Baishugou Formation within the boundary of the Nannihu-Sandaozhuang Mo deposits.

2.1. Nannihu-Sandaozhuang-Shangfanggou Mo-(W) Porphyry-Skarn Deposits

The Luanchuan ore field, which is situated in the western part of the East Qinling-Dabie Mo mineralization belt, includes the Nannihu Mo-(W) porphyry deposit, the Sandaozhuang Mo-(W) skarn deposit, and the Shangfanggou Mo-Fe porphyry deposit (Figure 2 and Figure 3) [50][68]. The total measured Mo reserves are more than 200 × 104 t, with a large W reserve of more than 70 × 104 t [51]. The outcropping strata consist of the Mesoproterozoic Guandaokou Group and the Neoproterozoic Luanchuan Group, comprising the Baishugou, Sanchuan, Nannihu, and Meiyaogou Formations, listed in ascending order. The Yanshanian metallogenic granite porphyry intrudes into the Nannihu Formation and the ore body occurs in the granite porphyry and altered biotite-feldspar hornfels in the Nannihu Mo-(W) porphyry deposit. Similarly, the thick-layered ore body is mainly hosted in the calc-silicate hornfels and the skarns in the upper Sanchuan Formation in the Sandaozhuang Mo-(W) skarn deposit (Figure 4). In the Shangfanggou Mo-Fe deposit, the Mo orebodies occur in the porphyritic biotite granite and its contact zones with the Meiyaogou Formation, including stone coal seams with thicknesses greater than 154 m, as well as in the altered gabbro. The layered Fe ores occur in the contact zone between the granite porphyry and the marble (Figure 5).
Figure 2. Simplified geology and distribution of Mo deposits in the East Qinling–Dabie Mo mineralization belt (after [68]).
Figure 3. Geological map of the Luanchuan Mo field (after [68]).
Figure 4. Geological section along the No. 9 exploration line in the Nannihu-Sandaozhuang W-Mo deposit (after [53]).
Figure 5. Geological map at the 1132 m level (A) and cross-section (B) of the Shangfanggou porphyry Mo deposit (after [27]).
The mineralization process can be divided Into four stages: (1) stage I, characterized by silicification, potassium and skarn alteration, with small amounts of magnetite and molybdenite; (2) stage II, the main Mo mineralization stage, characterized by intense silicification and sericitization, containing numerous quartz–K-feldspar–molybdenite veins, quartz–molybdenite veins and quartz–sulfide veins; (3) stage III, characterized by polymetallic sulfide mineralization, dominated by pyrite veins and quartz-sulfide-carbonate veins; and (4) stage IV, characterized by carbonate veins, quartz–carbonate veins and carbonate–fluorite veins, with almost no sulfides. Mineralization assemblages indicate a gradual decrease followed by an increase in the ore-forming system’s oxygen fugacity from the early to late stage.
The calcite in the Nannihu-Sandaozhuang-Shangfanggou Mo (W) porphyry-skarn deposits exhibits extremely low δ13CV-PDB values (−9.1‰ to −1.6‰, mean of −5.9‰), which are significantly different from those of the sedimentary marine carbonates in the Sanchuan Formation. This indicates that some carbon-enriched 12C originates from the carbonaceous rocks surrounding the deposits [53][55][69]. During ore formation, the δ13CV-PDB values of calcite gradually increase, but its δ18OV-SMOW values gradually decrease [69]. This suggests a decrease in the addition of CH4 from the carbonaceous surrounding rocks and an increase in the amount of atmospheric precipitation from the early to late stages, which is consistent with the redox state transformation revealed by mineral assemblages. During the mineralization process, carbonaceous surrounding rocks undergo thermal decomposition or react with hydrothermal fluids to produce CH4 and CO2, resulting in an increased CO2 concentration and a decreased oxygen fugacity in the ore-forming solutions. Sulfate is reduced to sulfide and combines with Mo2+ and other metallic elements to form much sulfide precipitation.

2.2. Shapinggou Porphyry Mo Deposit

The Shapinggou porphyry Mo deposit is in the eastern Dabie orogenic belt, with a total proven reserve of 1.6 Mt Mo metal, averaging a grade of 0.125% Mo. The main sedimentary layers exposed in this area are metavolcanic and metasedimentary rocks of the Neoproterozoic Luzhenguan Group, which is composed of biotite plagioclase gneiss, monzonite gneiss, plagioclase amphibolite gneiss, variolite, marble, muscovite schists, and graphite schists. Due to intense Yanshanian magmatic activity, the Luzhenguan Group is preserved as residual and captured bodies in the western and northern areas of this region (Figure 6) [70][71][72]. Graphite-mica-quartz schist and graphite-andalusite phyllite in the Xianrenchong Formation of the Luzhenguan Group are enriched to form graphite deposits in Jinzhai-Tiechongxiang-Zaohe (Figure 1A,B). Faults control the cylindric orebodies, which are mainly hosted in the contact zone between the porphyry granite and the surrounding diorite, with scattered orebodies distributed around the area. Lead-zinc and fluorite ores are abundant and encircle the Shapinggou deposit. The deposit shows well-defined alteration zoning of K (Na)-feldspar-quartz, pyrite-sericite-quartz, and chlorite-carbonate from the center granite porphyry outward. The mineralization process can be divided into four stages: (I) K (Na)-feldspar-quartz-magnetite/hematite stage; (II) quartz-K-feldspar-molybdenite stage, which is the main mineralization stage of molybdenite, dominated by quartz-(pyrite)-molybdenite veins in the contact zone between porphyry and surrounding rocks; (III) pyrite-sericite stage, characterized by abundant pyrite, sericitization, and silicification, with weak Mo mineralization; and (IV) quartz-fluorite-gypsum stage, characterized by abundant quartz-fluorite and gypsum veins (Figure 7). The above mineral assemblages indicate that the oxidation state of the mineralizing system gradually decreases from the early stage to the main ore-forming stage, and then increases in the late stage.
Figure 6. Geological map of the Shapinggou Mo deposit (modified from [71]).
Figure 7. Photographs of geological features in the Shapinggou porphyry Mo deposit. (A) Primitive magnetite developed in fresh quartz syenite from deep deposits. (B) Potassium alteration, silicification, and fluoritization from the early to late stages. (C) Potassium alteration and vein of molybdenite mineralization. (D) Sawtooth-shaped molybdenite filled in the fissures. (E) Later disseminated pyrite replaced earlier molybdenite. (F) White gypsum veins filled in the fractures in the late stage.
Due to the regional crustal uplift and erosion, the argillization, propylitic alteration zone, and vein-type Pb–Zn orebodies above the granite porphyry have been completely eroded, whereas the alteration zones and orebodies on both sides of the granite porphyry are preserved. The granite porphyry is now preserved approximately 400 m underground, with its top surface formed at a depth of approximately 2.2 km, and the erosion zone is estimated to be 1.8 km, making the main orebodies approach the surface. Most carbonaceous layers in the Luzhenguan Group in the Shapingou Mo deposit may have been eroded and distributed sporadically as remnants inside and outside the field.

2.3. Yuchiling Porphyry Mo Deposit

The Yuchiling deposit is a giant porphyry Mo deposit located west of the East Qinling–Dabie Mo mineralization belt in Henan Province, China. The main lithostratigraphic units are the Taihua Supergroup (basement) and the Xiong’er Group (cover) (Figure 8) [73]. The Taihua Supergroup, composed of a suite of amphibolite- to granulite-facies metamorphic rocks containing graphite-rich schist, is widely distributed in the Qinling-Dabie metallogenic belt. The carbonaceous sedimentary layers in the Taihua Supergroup, such as the Shuidigou Formation, containing carbonaceous mudstone and limestone, and the Huanchiyu Formation, composed of clastic, argillaceous, carbonaceous dolomitic limestone, and ferrimafic volcanic rocks, have formed graphite deposits in Lushan and Lingbao, respectively [60][61]. The Jidanping Formation and Majiahe Formation of the Xiong’er Group, which are predominantly composed of basaltic andesite, andesite, and dacite, are widely distributed north of the Machaoying Fault.
Figure 8. Geological map of the Yuchiling Mo deposit (after [73]).
The Heyu batholith is a concentrically zoned suite consisting of four nested, texturally distinguishable phases. There are breccia pipes genetically associated with Mo mineralization in the granite intrusion, which contain predominant granulite of the Taihua Supergroup and andesite of the Xiong’er Group. The orebody is mainly hosted in the top and bottom of the breccia and in the surrounding granite and fault zones in the central part of the Heyu batholith and occurs as a thick tabular shape with an average thickness of 178.11 m, showing decreasing grades upward [29][74][75]. The ore-forming processes can generally be divided into three stages: (I) molybdenite-K-feldspar stage, with pervasive potassic alteration and weak Mo mineralization. Fluid inclusions in this stage contain gypsum, hematite, and other highly oxidized minerals, indicating a high oxygen fugacity of fluids rich in SO42−. (II) The quartz-pyrite-molybdenite stage is characterized by veinlets, net veins, and disseminated molybdenite and pyrite (the main mineralization stage). Fluid inclusions contain less SO42− but show the presence of CH4, indicating a lower oxygen fugacity than the previous stage; (III) The quartz–fluorite-calcite stage is characterized by pyritic sericitization with weak mineralization. Fluid inclusions contain CH4 and C2H6, indicating a further decrease in oxygen fugacity during this stage [28][29].
The Yuchiling deposit contains a shallowly buried orebody spanning from 730 to 190 m in elevation. The deposit displays an outcrop of the orebody and the mineralized porphyry, suggesting that it has undergone extensive tectonic uplift and erosion since its formation. The widespread graphite-bearing phyllite of the Taihua Supergroup and volcanic rocks of the Xionger Group, which existed during the formation of the deposit, have been significantly eroded and now exist only in the breccia pipes situated in the southwestern and northeastern parts of the mining area. It is possible that the graphite-bearing phyllite of the Taihua Supergroup may have played a role in the formation of the deposit by providing CH4 as a reductive agent, thereby reducing the oxidized porphyry and efficiently facilitating sulfide precipitation.

2.4. Mt. Emmons Porphyry Mo Deposit

Mt. Emmons lies in the west-central portion of the Colorado (Climax-Henderson) Mo mineralization belt on the eastern coast of the Pacific Ocean. Giant or large Mo deposits, such as the Urad-Henderson, Climax, Mt. Emmons, and Silver Creek deposits, are developed in this belt (Figure 9A). The Mt. Emmons ore field contains two deposits below the Redwell Basin and a third deposit under the Red Lady Basin (Figure 9B). The surrounding sedimentary rocks of the Mancos and Mesaverde Formations consist of dark carbonaceous shale and sandstone beds, which are capped by conglomeratic sandstone beds of the Tertiary Ohio Creek and Wasatch Formations [76]. The granite porphyry stocks intrude the carbonaceous surrounding rocks, forming an altered hornfel contact zone bearing pyrite-pyrrhotite. The black carbonaceous surrounding rocks are altered and discolored, and an innermost 300 m-thick facies of brown hornfels surrounding the stocks grade outward to a 150 m-thick facies of black hornfels [25][77].
The Climax and Urad-Henderson superlarge Mo deposits have geological characteristics and mineralization ages similar to those of the Mt. Emmons deposit. Orebodies occur in the Mesoproterozoic silver plume granite pluton [3][4][78][79]. Previous studies have demonstrated the prevalence of carbonaceous shale, sandstone, mudstone, oil shale, and coal within the Wasatch Formation and the Mesaverde Group in Wyoming and Utah in Colorado [25][62][63][64][65][66][67]. Technically, the mean recoverable gas resources have been estimated at 7 × 1012 m3 with primary sources being coal, carbonaceous shale and siltstone in the Mesaverde Group [80]. In this region, dark carbonaceous shale and mudstone serve as the dominant hydrocarbon sources, providing reductive agents and effective water-resisting layers for mineralization. The absence of carbonaceous sedimentary layers from the Wasatch Formation and Mesaverde Group in the Climax and Urad-Henderson Mo deposits may be attributed to regional crustal uplift and erosion.
Figure 9. (A) Map of Colorado showing the locations of the Urad–Henderson, Mt. Emmons and Silver Creek porphyry Mo deposits and the outlines of the Colorado Mineral Belt; (B) Schematic cross-section through the porphyry Mo deposits in the Redwell Basin and Mt. Emmons, Colorado, in America (modified from [40][46][77]). Black carbonaceous sedimentary layers are widespread in porphyry Mo deposits. Due to tectonic uplift and erosion in some areas, the reductive carbonaceous rocks that once covered the Mo deposits have been completely eroded, such as at the Climax and Urad-Henderson porphyry Mo deposits in America [79]. Carbonaceous rocks may remain only at the periphery of the mining area, such as at the Yuchiling porphyry Mo deposit [73], or appear sporadically in the form of remnants inside and outside the mining area, such as at the Shapinggou porphyry Mo deposit [71]. Notably, the development of reductive components such as graphite ores/coal, dark carbonaceous mudstone/limestone, and natural gas nearby indicates that pre-existing carbonaceous surrounding rocks involved in porphyry Mo mineralization may have been eroded in these deposits. Carbonaceous surrounding rocks provide reductive agents for oxidizing ore-forming fluids and promote sulfate reduction to form Mo and other mineral ores, which is an essential factor for forming large high-grade porphyry Mo deposits.

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