Abstract
The Jiaodong gold concentration area, one of the most important gold metallogenic belts in China, has long been the focus of contentious debates regarding the genetic mechanisms and timing of gold mineralization. This study presents the new monazite U-Pb and pyrite Rb-Sr isotopic chronology data for the No. I ore zone of the Xidouya gold deposit, integrated with H-O-S isotopic geochemical analyses, to systematically investigate the mineralization age, ore-forming fluid sources and material provenance of the deposit. The main mineralization age of the deposit is constrained to 117 Ma, which is highly consistent with the regional mineralization peak of 120 ± 5 Ma in the Jiaodong gold concentration area. The δD values of the fluids range from −88.0‰ to −75.0‰ (mean = −82.6‰), while the δ18OH2O values are calculated to be between 4.6‰ and 6.1‰. H-O isotopic data indicate that the ore-forming fluids of the Xidouya gold deposit originated from a mixed magmatic and meteoric source. As mineralization progressed from Stage I through Stage III, there was a detectable trend of increasing meteoric water involvement and a general decrease in δD and δ18OH2O values. This signature indicates that the initial mineralizing system was dominated by primary magmatic water which subsequently underwent significant water–rock interaction with Early Cretaceous granitic bodies and progressive dilution by meteoric fluids in an open tectonic environment. Furthermore, sulfur isotopes (average δ34S = +7.43‰) and the initial strontium isotope ratio (87Sr/86Sr = 0.71012) support a mixed-source model for the ore-forming materials, likely dominated by the anatexis of ancient crust with potential minor mantle-derived contributions. During the Early Cretaceous, lithospheric thinning and extension in the North China Craton (NCC) triggered large-scale magmatism and mineralization. The Xidouya gold deposit is a direct product of these regional tectono-magmatic-mineralizing events. This study provides new high-precision isotopic dating data for the Xidouya gold deposit, clarifies the evolutionary history of ore-forming fluids and the supply mechanism of ore-forming materials, and provides important theoretical insights and practical references for gold prospecting and exploration in the eastern part of the Jiaodong gold concentration area.
1. Introduction
The Jiaodong gold concentration area represents a major gold resource base in China with favorable metallogenic conditions, hosting proven gold resources of 5800 t [1,2,3,4]. It can be further subdivided into three concentration areas from west to east: the Jiaoxibei (Zhaoyuan–Laizhou), Qipengfu (Qixia–Penglai–Fushan) and Muru (Muping–Rushan) gold concentration areas [5,6]. The large to super-large gold deposits are predominantly distributed in the Jiaoxibei gold concentration area, whereas the Qipengfu gold concentration area is dominated by small and medium-sized gold deposits [7]. The Xidouya gold deposit investigated in this study is located in the Qipengfu gold concentration area, with proven gold reserves of 11.56 t [8]. As one of the few gold deposits with reserves exceeding 10 t in this concentration area, it is adjacent to the Hushan gold deposit with reserves of nearly 20 t [7]. The discovery of these two medium-to-large gold deposits demonstrates the significant metallogenic potential of this region. In-depth research on the Xidouya gold deposit not only serves as a key supplement to the gold metallogenic patterns of the Qipengfu gold concentration area but also challenges the traditional perception that only small and medium-sized deposits are present in this area. The mineralized concentration area formed by the Xidouya and Hushan gold deposits provides a typical case for analyzing the ore-controlling structures, mineralization age, ore-forming fluid evolution and gold enrichment mechanisms of the Qipengfu gold concentration area, and the research findings will also offer important theoretical and practical guidance for gold prospecting and exploration in the eastern part of the entire Jiaodong gold concentration area.
In recent years, the controlling effects of Mesozoic granites on gold mineralization have attracted extensive attention from geoscientists worldwide. Similarly, the role of the lithospheric mantle in regulating gold mineralization has also become a major research focus. Some researchers propose that metasomatism of the convective mantle or subducted slab materials and their overlying sediments may lead to the anomalous enrichment of gold and volatiles in the mantle, which could represent the source of ore-forming fluids and materials for gold deposits in the Jiaodong gold concentration area [9,10,11]. Other researchers argue that the ore-forming materials of gold deposits were derived from the metasomatically enriched lithospheric mantle during subduction events, with the incorporation of crustal components during migration [12,13,14]. A consensus has been reached that the main phase of gold mineralization in the Jiaodong gold concentration area occurred at 120 ± 5 Ma [15,16,17,18]. Some studies suggest a west-to-east younging trend of mineralization ages across the province [19,20].
Previous studies have been conducted on the geological characteristics, deep prospecting potential, and implications of fluid inclusions for ore-forming fluid evolution of the Xidouya gold deposit, yielding preliminary understandings [7,21,22,23,24]. Some researchers have proposed that the Xidouya gold deposit is an epigenetic mesothermal-to-epithermal hydrothermal-altered cataclastic rock-type deposit with favorable prospecting potential in the deep and peripheral areas [22]. Others suggest that the No. I orebody of the Xidouya gold deposit is contiguous with that of the Hushan gold deposit, belonging to a single deposit with total gold reserves reaching 30 t (a large gold deposit) [7]. Additionally, studies on the No. II orebody of the Xidouya gold deposit indicate that the ore-forming fluids are dominated by mixed magmatic and meteoric water, characterized by mesothermal to epithermal temperatures, moderate to low salinity and low density, with a mineralization depth ranging from 5.81 to 7.82 km [23]. However, the aforementioned studies are relatively limited in investigating the relationship between Mesozoic tectono-magmatic activities and gold mineralization, as well as the source of ore-forming materials and the precise mineralization age. The genetic type of the gold deposit and the tectonic dynamic setting of mineralization remain unclear.
The widely developed quartz–pyrite–polymetallic sulfide gold ores in the Xidouya gold deposit provide a new opportunity to elucidate the timing and genesis of gold mineralization. As the most common gold-bearing sulfide in gold deposits, pyrite is a direct recorder of fluid activity and material migration during mineralization [17]. U-Pb isotope analysis was conducted on monazite separated from the gold-bearing quartz–pyrite veins within the main ore body of the Xidouya gold deposit, combined with Rb-Sr isotope analysis of pyrite, to precisely constrain the mineralization age of the deposit. Based on detailed geological evidence and petrographic characteristics, the newly obtained isotopic chronology data are interpreted as the precise mineralization age of the Xidouya gold deposit. Using the H-O-S isotopic compositions, we reconstruct the physico-chemical conditions of mineralization, clarify the origin and evolutionary process of ore-forming fluids, identify the end-members of ore-forming material supply, and discuss the deposit genesis, thereby providing key geochemical evidence for summarizing regional metallogenic regularity and guiding gold prospecting and exploration.
2. Regional Geological Setting
The Jiaodong gold concentration area is tectonically located at the southeastern margin of the North China Craton (NCC), consisting of the Jiaobei Uplift in the north, the Jiaolai Basin in the central part and the Jiaodong Terrane in the southeast (Figure 1a) [25,26,27,28]. The Jiaobei Uplift and the Jiaodong Terrane are bounded by the Muping–Jimo Fault, which also constitutes the suture zone between the North China Craton and the Yangtze Craton [26,27]. The Qipengfu gold concentration area is situated within the Jiaobei Uplift, where the metamorphic basement is well developed, mainly comprising the Neoarchean tonalite–trondhjemite–granodiorite (TTG) gneiss suite with Triassic ultra-high-pressure metamorphic rocks (UHP gneiss) [29]. The exposed strata include the Neoarchean biotite leptynite, plagioclase amphibolite, hornblende leptynite intercalated with magnetite quartzite assemblage, Paleoproterozoic meta-sedimentary rocks, Neoproterozoic slate and sandstone, Early Cretaceous volcanic sedimentary rocks, and Quaternary sediments (Figure 1b) [30]. Mesozoic intrusive rocks are extensively developed, mainly including the Late Jurassic granites (Linglong granite) and Early Cretaceous granites (Guojialing granite, Weideshan granite and Yushan granodiorite porphyry) [6]. In addition, various dykes such as Mesozoic lamprophyre, diabase and quartz diorite dykes are widely distributed throughout the area.
The Jiaodong gold concentration area is characterized by well-developed ductile shear zones and brittle fault structures. Ductile shear zones are mainly exposed in the ancient metamorphic basement; the Archean Qixia granite–greenstone belt is featured by widespread striped and banded structures in rocks, accompanied by numerous small folds of various morphologies, with elongated “school-of-fish” mafic rock inclusions visible within the zones [31]. Brittle fault structures are dominated by NNE- and NE-trending faults, which are closely associated with gold mineralization, with scattered EW-, NW- and SN-trending faults interspersed among them (Figure 1b). These brittle faults and their associated secondary and tertiary fault systems provide essential channels and reservoir spaces for the migration, enrichment and precipitation of ore-bearing hydrothermal fluids.
Figure 1.
Regional distribution and simplified geological map of the Jiaodong Peninsula (modified after [25,32]). (a) The tectonic division for the Jiaodong Peninsula between the North China Craton and the Sulu orogen along the Tan–Lu Fault. (b) Simplified geology in the Jiaodong Peninsula.
Figure 1.
Regional distribution and simplified geological map of the Jiaodong Peninsula (modified after [25,32]). (a) The tectonic division for the Jiaodong Peninsula between the North China Craton and the Sulu orogen along the Tan–Lu Fault. (b) Simplified geology in the Jiaodong Peninsula.

3. Ore Deposit Geology
The stratigraphy in the study area is relatively simple. The basement lithology of the mining area is primarily composed of Paleoproterozoic metamorphic strata, which are dominated by fine-grained biotite leptynite with local enclaves of tremolite-feldspar-quartzite (Figure 2a). In addition, Quaternary sediments, such as sandy clay and conglomerate, are distributed across the surface of the mining area. The surface-exposed magmatic rocks mainly include Meso-Neoarchean gneissic hornblende–trondhjemitic gneiss and fine-grained hornblende trondhjemite, Early Neoarchean plagioclase amphibolite, Late Jurassic porphyritic medium-coarse grained monzogranite, and the dykes are mainly Late Yanshanian quartz diorite dykes (Figure 2) [22].
Figure 2.
Geological map of the Xidouya gold deposit (a) and the exploration profile of line 65 (b) (modified after [23]).
The NE-trending Taiqian–Douya Fault Zone runs through the entire study area and represents the first-order fault in the mining area. The fault has a total length of 36 km, with a strike of approximately 30–40°, dipping southeast at an angle of 28–35° and a length of about 3 km within the study area [22]. The fault is mostly developed near the contact zones of different rock masses and exhibits distinct polyphase activity characteristics. Early-stage activity formed mylonite and cataclasite; middle-stage activity was characterized by extensional (transtensional) features with breccias of various sizes; late-stage activity transformed into a transpressional fault with extensive grayish-white cataclasite and mylonite developed [23]. Disseminated and veinlet pyritization can be observed in the deep part of the fault. NNE-trending secondary faults developed in groups in the footwall of this fault, and several faults with roughly parallel strikes and close spacing form a composite fault zone. All ore-bearing altered zones in the area are strictly controlled by the above types of faults.
Orebodies are mainly located in the footwall of the Taiqian–Douya Fault Zone, with their occurrence and scale strictly controlled by the fault system, and the host rocks are mainly porphyritic medium–coarse-grained monzogranite. There are seven industrially valuable orebodies in the deposit, represented by No. I, VI and IX orebodies [22]. This study selects the No. I orebody for a detailed description, which can be further divided into the No. I-1 main orebody and the No. I-2 minor orebody. The No. I-1 orebody occurs as vein and lenticular shapes, with a strike of 23–29°, dipping southeast at an angle of 25–30° (Figure 2b). It extends about 700 m along the strike and 450 m along the dip, with a thickness ranging from 0.87 to 25 m and an average thickness of approximately 5.12 m. The gold grade varies from 1.12 ppm to 13.31 ppm, with an average grade of 3.28 ppm and a maximum grade of 13.31 ppm in a single sample [21]. The No. I-2 orebody is lenticular and vein-shaped, with a strike of 20–36°, dipping southeast at an angle of 28–30°. It stretches about 485 m along the strike and 350 m along the dip, with a thickness of 1.0–6.3 m (average 1.34 m) and a gold grade of 1.74–4.02 ppm (average 2.85 ppm) [21].
The ores exhibit a variety of textures, dominated by crystalline granular, metasomatic relict, interstitial and euhedral–subhedral textures. The ore structures are mainly disseminated and brecciated structures. The mineral composition is relatively simple; metallic minerals are mainly native gold and pyrite, with minor pentlandite, pyrrhotite and chalcopyrite (Figure 3). Gangue minerals are mainly quartz, sericite and carbonate minerals. Native gold occurs mainly as angular grains, followed by elliptical grains, and is primarily hosted in the interior of pyrite grains and intergranular fractures of pyrite, with a grain size generally less than 50 μm (Figure 3). Hydrothermal alteration types mainly include pyritization, potassic alteration, propylitization (including zoisitization, epidotization and clinozoisitization), sericitization, silicification and carbonatization.
Figure 3.
Representative photographs of outcrops and photomicrographs of samples from the Xidouya gold deposit. (a–c) Field outcrop photographs showing the spatial relationship between two stages of mineralized veins. Stage I (Qtz) consists of early-stage milky quartz veins, which occur as banded bodies, are relatively pure, and contain well-developed microfractures. Stage II (Qtz + Py) quartz–pyrite polymetallic sulfide veins developed along both sides of Stage I veins, exhibiting a bedding-parallel relationship. (d) Hand specimen photograph of pyrite-bearing polymetallic sulfide ore, with a mineral assemblage of quartz, pyrite, and pentlandite. (e) Photomicrograph (reflected light) showing native gold occurring as granular particles in the intercrystalline spaces or fractures of pyrite, with quartz present as a gangue mineral. (f) Photomicrograph (reflected light) showing native gold occurring as fine inclusions within pyrite. (g) Assemblage of monazite and pyrite. Abbreviations: Qtz: Quartz; Au: Gold; Py: Pyrite; Pn: Pentlandite; Mnz: Monazite.
Based on mineral paragenetic associations and cross-cutting relationships, the mineralization process of the deposit is divided into three distinct stages: I, Au–quartz–pyrite stage; II, Au–quartz–polymetallic sulfide stage (the main mineralization stage); III, quartz-carbonate stage [22].
4. Sampling and Analytical Methods
Samples for experimental analysis were collected from the No. I ore zone of the Xidouya gold deposit at a depth of −100 to −105 m, including ore types of quartz–pyrite and quartz–polymetallic sulfide. Polished sections were prepared for ore microscopic and petrographic observations, and some samples were completely ground to separate single minerals, followed by mount preparation and photography. H-O-S isotopic analyses were conducted at the Key Laboratory of Metallogenic Processes and Resource Assessment, Ministry of Natural Resources, Institute of Mineral Resources, Chinese Academy of Geological Sciences, Beijing, China. Isotopic chronology analyses were all completed at the Isotopic Chronology Laboratory, Tianjin Center, as part of the China Geological Survey, Tianjin, China.
4.1. H-O Isotope Analysis
Quartz from each mineralization stage was selected for H-O isotopic analysis. Samples were crushed to 40–60 mesh, and pure quartz single minerals (purity > 99%) were carefully hand-picked under a binocular microscope. Analyses were performed on a MAT-251EM mass spectrometer (Finnigan MAT GmbH, Bremen, Germany), with an analytical precision of ±0.2‰relative to the Vienna Standard Mean Ocean Water (V-SMOW) standard. δD values were determined by the Zn reduction method for hydrogen production: water was extracted from fluid inclusions in quartz by the vacuum thermal decrepitation method, and the extracted water reacted with high-purity Zn at 400 °C to generate H2 for mass spectrometric analysis [33]. δ18O values were measured by the BrF5 equilibration method: quartz single minerals reacted with BrF5 at 450–550 °C for nearly 2 h to produce oxygen, and pure oxygen was obtained by separating impurities such as SiF4 and BrF3 using a combined cold trap. The purified oxygen reacted with carbon rods step by step at 700 °C under platinum catalysis, and the generated CO2 gas was collected sequentially for mass spectrometric analysis [34].
4.2. S Isotope Analysis
Fresh and pure pyrite single minerals (purity > 99%) were hand-picked after crushing the ore samples. Sulfide samples were oxidized to SO2 with Cu2O as the oxidant under high-vacuum conditions at 1000 °C for 15 min, and the generated SO2 was used for sulfur isotope analysis. The analysis was carried out on a MAT-251EM mass spectrometer relative to the Vienna Canyon Diablo Troilite standard, with an analytical precision of ±0.2‰.
4.3. Monazite U-Pb Dating
Monazite single minerals were separated from quartz-pyritized ores of the mineralization Stage II. Backscattered electron (BSE) images of monazite were obtained at the Experimental Testing Laboratory, Tianjin Center, China Geological Survey. U-Pb isotopic dating was performed using a New Wave 193 nm laser ablation system coupled with a Thermo Fisher Neptune (Thermo Fisher Scientific, Bremen, Germany) multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS). The laser spot diameter for monazite analysis was 25 μm, with a pulse frequency of 5 Hz and a laser energy density of 10–11 J/cm2. The monazite standard 44069 (pale-yellow euhedral equigranular monazite from the Wilmington Complex, Delaware, USA) was used for external calibration. Detailed experimental procedures refer to previous studies [35,36]. Data processing was conducted using the ICPMSData program [37], and weighted mean age calculation and concordia diagram plotting were completed with the Isoplot program [38,39]. Experimental analytical errors were reported at the 1σ level.
4.4. Pyrite Rb-Sr Dating
Rb-Sr isotopic analysis was also separated from quartz-pyritized ores of the mineralization Stage II, with a total of eight samples selected for analysis. To ensure the isotopic signature accurately reflected the primary ore-forming fluid and to eliminate potential contamination from late-stage carbonate veins or secondary inclusions, the pyrite grains were subjected to rigorous ultrasonic cleaning and a sequential acid-leaching procedure prior to dissolution. Following this purification step, appropriate amounts of the pyrite samples were accurately weighed and dissolved using a mixed acid solution of HNO3 and HClO4. The dissolved sample solution was evenly divided into two parts: one part was spiked with an appropriate amount of 87Rb + 84Sr mixed diluent, and after chemical separation and purification, it was used for the determination of Rb and Sr content; the other part was used for the determination of Sr isotopic ratios after separation and purification. The Rb and Sr separation procedure adopted the traditional AG50W × 12 cation exchange resin separation process, with gradient elution using HCl solutions of different concentrations to collect Rb and Sr fractions separately. Rb and Sr isotopic analyses were performed on a TRITON thermal ionization mass spectrometer (TIMS, manufactured by Thermo Fisher Scientific, Bremen, Germany). Specific experimental separation procedures and instrumental test parameters refer to previous studies [40] and isochron age calculation was completed with the Isoplot program [38,39].
5. Results
5.1. H-O Isotopic Compositions of Quartz
A total of nine sets of H-O isotopic data were obtained in this study, combined with three sets of previously published data (Table 1). The δD values range from −88.0‰ to −75.0‰ with an average of −82.6‰, and the δ18O values vary from 10.3‰ to 12.2‰ with a mean of 11.2‰. The hydrogen isotopic composition of the ore-forming fluid is consistent with that of water in quartz fluid inclusions, and the oxygen isotopic composition of the fluid was calculated based on the oxygen isotopic composition of quartz and the mineralization temperature of different stages. To calculate the oxygen isotopic composition of the fluid (δ18OH2O), the maximum homogenization temperature of the fluid inclusions at each stage was used. Because the homogenization temperatures generally represent the lower limit of the actual mineralization temperature, and our studied system lacks clear evidence of fluid boiling, applying the maximum homogenization temperature provides the most reasonable approximation to the true trapping conditions during mineralization. Previously measured homogenization temperatures of fluid inclusions for stages I, II and III of the No. I ore zone in the Xidouya gold deposit are 323 °C, 336 °C, and 353 °C, respectively [24]. Based on the oxygen isotope fractionation equation between quartz and water, “1000lnαQ−W = 3.38 × 106/T2 − 2.90” [41], the oxygen isotope composition δ18OH2O of water in the mineralizing hydrothermal fluid is estimated as follows: δ18OH2O = δ18OSMOW − 1000lnαQ−W.
Table 1.
Hydrogen and oxygen isotope compositions in the Xidouya gold deposit.
In terms of different mineralization stages, the fluid in Stage I has δD values of −81.0‰ to −75.0‰ (average −77.7‰, n = 3), δ18O values of 11.8‰ to 12.2‰ (average 12.0‰), and δ18OH2O values of 5.7‰ to 6.1‰ (average 5.9‰). The fluid in Stage II exhibits δD values of −86.0‰ to −79.0‰ (average −83.0‰, n = 6), δ18O values of 10.3‰ to 11.5‰ (average 10.9‰), and δ18OH2O values of 4.6‰ to 5.8‰ (average 5.2‰). The fluid in Stage III has δD values of −88.0‰ to −85.0‰ (average −86.7‰, n = 3), δ18O values of 10.6‰ to 11.1‰ (average 10.9‰), and δ18OH2O values of 5.4‰ to 5.9‰ (average 5.6‰).
5.2. S Isotopic Compositions
S isotopic studies were mainly conducted for Stage I and II of mineralization, with a total of 14 sets of new S isotopic data obtained and 22 sets of previously published data collected, amounting to 36 sets of data in total (Table 2). The δ34S values show a narrow range of variation from 5.82‰ to 8.63‰ with an average of +7.43‰, all positively deviated from meteoritic sulfur (δ34S = 0‰) (Figure 4). By stages, the δ34S values of pyrite in the ore-forming fluid of Stage I range from 7.51‰ to 8.63‰ with an average of 8.13‰. In Stage II, the δ34S values of pyrite in the ore-forming fluid vary from 5.93‰ to 8.22‰ (average 7.44‰), and the δ34S values of chalcopyrite range from 5.82‰ to 6.85‰ (average 6.30‰).
Table 2.
Sulfur isotopic analyses in the Xidouya gold deposit.
Figure 4.
The sulfur isotope compositions of pyrite from the Xidouya gold deposit as well as those from other geological units in Jiaodong. The Intermediate–basic Diles complex δ34S data from [42]. The Early Cretaceous granitic complex δ34S data from [43]. The Late Jurassic granitic complex δ34S data from [43,44]. The Jingshan group δ34S data from [45]. The Jiaodong group δ34S data from [43,46,47,48].
5.3. Monazite U-Pb Ages
Monazite grains recovered from the Stage II quartz–pyrite veins are dark gray and exhibit euhedral to subhedral morphologies, with grain sizes typically ranging from 50 to 100 μm (Figure 5). Th content is an effective geochemical indicator for distinguishing monazite genetic types: hydrothermal monazite typically has low U and Th content, with highly variable Th/U ratios in low-temperature metamorphic and hydrothermal monazite; high-grade metamorphic and magmatic monazite have high Th contents, usually greater than 3% [49,50]. Backscattered electron (BSE) imaging reveals that these grains possess a homogeneous internal texture and lack obvious compositional zoning—features that are consistent with a hydrothermal rather than a magmatic or high-grade metamorphic origin (Figure 5). Furthermore, the maximum Th content is approximately 2.3%, which provides additional support for a hydrothermal genesis (Table 3). Notably, two monazite grains yielded older 206Pb/238U ages of 132.7 Ma and 123.4 Ma (Table 3). Based on their distinct textural positioning and older isotopic signatures, these grains are interpreted as inherited relicts derived from the host wall-rock; consequently, they were excluded from the final age calculation. The remaining 26 analyses plot on or closely along the concordia line, yielding a weighted mean 206Pb/238U age of 116.69 ± 1.2 Ma (MSWD = 2.4) (Figure 6). Given their paragenetic association with the primary sulfide minerals and their geochemical characteristics, this date is interpreted to represent the timing of the syn-ore hydrothermal event.
Figure 5.
Backscattered images of Monazites from the pyrite–quartz vein in the Xidouya gold deposit.
Table 3.
Monazite LA-ICP-MS U-Pb data for spot analysis.
Figure 6.
Monazite U-Pb concordia diagrams of the Xidouya gold deposit.
5.4. Pyrite Rb-Sr Ages
Rb-Sr isotopic analysis of eight pyrite samples from the mineralization Stage II (Table 4) shows that the 87Rb/86Sr ratios range from 0.7351 to 20.3274, and the measured (87Sr/86Sr) ratios vary from 0.711461 to 0.743643, with a good linear relationship observed in the 87Rb/86Sr vs. 87Sr/86Sr diagram (Figure 7). The isochron age of pyrite calculated using the ISOPLOT 3.0 software [39] is 117.2 ± 3.3 Ma, with an initial 87Sr/86Sr ratio of 0.71012 ± 0.00042 (MSWD = 1.02) (Figure 7).
Table 4.
The mass fractions and isotope ratios of Rb and Sr in pyrite from the Xidouya gold deposit.
Figure 7.
Rb-Sr isotope data and isochron ages of pyrite from the Xidouya gold deposit. The numbers (1.1–1.8) are meaning the sequence no. in Table 4.
6. Discussion
6.1. Mineralization Timing
Precise determination of mineralization timing is the key to understanding deposit genesis and regional metallogenic regularity. This study carries out high-precision monazite U-Pb and pyrite Rb-Sr isotopic dating for the Xidouya gold deposit. The hydrothermal monazite separated from quartz–pyrite ores of the mineralization Stage II yields a weighted mean 206Pb/238U age of 116.69 ± 1.2 Ma (MSWD = 2.4). Monazite can crystallize directly from ore-forming fluids in hydrothermal deposits and has a high closure temperature for the U-Pb isotopic system, which can effectively record the precise timing of hydrothermal mineralization activity [51,52,53]. This age can be reliably interpreted as the main mineralization age of the Xidouya gold deposit.
Pyrite is a ubiquitous and dominant sulfide mineral in hydrothermal gold deposits, typically precipitating synchronously with the main ore-forming processes. During its crystallization from hydrothermal fluids, trace amounts of rubidium (Rb) and strontium (Sr) can be incorporated into the pyrite lattice or trapped within primary fluid inclusions. Because the Rb-Sr isotopic system in pyrite is characterized by a relatively high closure temperature, it strongly resists isotopic resetting from subsequent low-temperature thermal or tectonic events [17,54,55,56,57]. Consequently, pyrite Rb-Sr isochron dating has been proven to be a highly reliable and robust method for directly determining the absolute timing of hydrothermal mineralization, accurately reflecting the age of the ore-forming fluid activity [17,54]. The pyrite Rb-Sr isochron age of the same mineralization stage is 117.2 ± 3.3 Ma, with an initial 87Sr/86Sr ratio of 0.71012 ± 0.00042 (Figure 7). This age is in good agreement with the monazite U-Pb age within analytical errors, and the two independent isotopic dating methods mutually corroborate each other, precisely constraining the main mineralization age of the Xidouya gold deposit to 117 Ma. This age is highly consistent with the mainstream regional mineralization peak of 120 ± 5 Ma in the Jiaodong gold concentration area [15,18,19,57,58,59], indicating that the Xidouya gold deposit is a typical product of the large-scale regional gold mineralization event in the Early Cretaceous.
6.2. Ore-Forming Fluid Source
H-O isotopic composition is a powerful and effective geochemical tool for tracing the origin of ore-forming fluids, which has been widely used to constrain the source of ore-forming fluids for various genetic types of mineral deposits [60,61]. In this study, the δD values of ore-forming fluids in different mineralization stages range from −88.0‰ to −75.0‰ with an average of −82.6‰, which falls entirely within the typical δD range of mixed magmatic and meteoric fluids, indicating that the ore-forming fluids are not dominated by metamorphic water (Figure 8). Extensive H-O isotopic studies have been conducted in the Jiaodong gold concentration area by previous researchers, yielding a relatively mature understanding of the H-O isotopic geochemical background of major rocks and fluids in this area. The δ18OSMOW values of the Jiaodong Group strata range from 5.1‰ to 11.3‰, and the δD values vary from −96‰ to −81‰ [62]. Previous determinations of δD compositions of biotite in Late Jurassic granites and Early Cretaceous granodiorites in the Jiaodong gold concentration area show that the δD ranges of the two rock types are −72 ± 11‰ and −102 ± 15‰ [63], respectively, with corresponding δ18OSMOW values of < 7‰ and 10.1 ± 0.4‰ [64,65]. Accurate H-O isotopic background values of Mesozoic meteoric water in the Jiaodong gold concentration area have also been obtained by previous geochemical calculations [65,66].
Figure 8.
Isotopic compositions of oxygen and hydrogen in the Xidouya gold deposit (modified after [67,68]). Regions A, B, and C represent the mixing areas of meteoric water with metamorphic water of the Jiaodong Group, magmatic water of Late Jurassic granite, and magmatic water of Early Cretaceous granite, respectively.
From the δD-δ18OH2O isotopic cross-plot (Figure 8), it can be found that the H-O isotopic compositions of quartz from the Xidouya gold deposit show a good overlap with Zone A (mixed fluid zone of primary magmatic water and meteoric water of the Jiaodong Group) and Zone C (mixed fluid zone of Early Cretaceous primary magmatic water and meteoric water). Previous sampling and dating of granodiorite in the deep part of the Xidouya gold deposit yielded an age of 127.8 ± 1.1 Ma [23], indicating the presence of an Early Cretaceous granite body in the deep part of the deposit. Ore-forming fluids underwent intense water–rock interaction with this granite body during migration and ascent, which significantly affected the geochemical properties of the ore-forming fluids. The average δ18OH2O value of the ore-forming fluid in Stage I is 5.9‰, which is close to the characteristic range of magmatic water (5‰–10‰), suggesting the presence of a magmatic water-dominated fluid in the early stage. The average δ18OH2O value of Stage II drops to 5.2‰, reflecting an increased incorporation of meteoric water into the fluid system. The average δ18OH2O value of Stage III slightly increases, but the δD and δ18OH2O values of the ore-forming fluid show an overall decreasing trend with the evolution of mineralization from Stage I to III. While other fluid models cannot be entirely ruled out, these geochemical characteristics are highly compatible with a mixed fluid system that underwent progressive meteoric water influx and fluid–rock interaction during migration.
6.3. Ore-Forming Processes
Sulfur isotope is a core geochemical indicator for tracing the source of ore-forming materials in hydrothermal mineral deposits. The sulfide δ34S values obtained in this study range from 5.82‰ to 8.63‰ with an average of 7.43‰, showing a narrow and concentrated distribution with a consistent positive deviation from meteoritic sulfur (δ34S = 0‰), which is highly consistent with the sulfur isotopic characteristics of major geological bodies in the Jiaodong gold concentration area. These geochemical characteristics suggest that the sulfur source of the Xidouya gold deposit is not derived from a single end-member. Instead, the data support a mixed-source hypothesis, predominantly involving anatectic ancient crustal materials with a potential minor contribution of mantle-derived sulfur. The δ34S values are relatively high in Stage I and distinctly lower in Stage II, and this evolutionary trend is closely related to the regional tectonic stress transition from compression to extension in the Early Cretaceous (Figure 4). Extensional tectonics provided open pathways for fluid migration and increased the oxidation state of the mineralization environment. This oxidizing environment intensified sulfur isotope fractionation, resulting in δ34S values that are consistently higher in pyrite than in chalcopyrite. This distinct fractionation pattern strongly indicates a multi-source origin for the ore-forming sulfur. The host rocks of the mining area are Paleoproterozoic metamorphic rocks and Mesozoic granites, and sulfur in these rocks can generate crust-derived sulfur with high δ34S values through metamorphism and anatexis, providing an important material basis for gold mineralization in the Xidouya deposit.
The initial pyrite Rb-Sr isotopic ratio (0.71012 ± 0.00042) falls between typical mantle (0.703–0.707) and average crustal (0.715–0.720) compositions. While this is consistent with a crust–mantle mixing signature, it is important to note that such isotopic values can also result from the assimilation of highly radiogenic crustal fluids. Based on sulfur and strontium isotopic data, the Xidouya gold deposit is characterized by a typical “crust–mantle mixed” source system. The ore-forming materials were mainly derived from the host monzogranite’s source region, which is dominated by melted ancient crust, and later incorporated Early Cretaceous granitic crustal components during fluid ascent.
6.4. Metallogenic Geodynamic Setting
This Early Cretaceous metallogenic event occurred within a well-established regional geodynamic framework characterized by the destruction of the North China Craton. Combined with the regional tectonic evolution background, the North China Craton experienced extensive lithospheric thinning and the establishment of an extensional tectonic regime during the Early Cretaceous (135–110 Ma) [15,69,70,71]. Before 135 Ma, the Paleo-Pacific Plate subducted slowly toward the northwest. During 135–125 Ma, the subduction direction gradually rotated clockwise and the subduction rate accelerated significantly. After 125 Ma, the sudden break-off and rollback of the subducting Paleo-Pacific Plate triggered a regional tectonic shift from a transpressional to a transtensional regime. This Early Cretaceous transition drove subsequent lithospheric extension, thinning, and asthenospheric upwelling [15,69,70,71].
These deep-seated processes provided a highly favorable geodynamic setting for large-scale gold mineralization in the Jiaodong concentration area. The mineralization age of the Xidouya gold deposit coincides exactly with the peak of this tectono-magmatic activity, indicating that the formation of the deposit is closely related to mantle partial melting, crustal material anatexis and intense hydrothermal fluid activity induced by lithospheric extension. Its metallogenic dynamic setting is thus controlled by the regional tectono-magmatic events during the destruction of the North China Craton in the Early Cretaceous.
7. Conclusions
Consistent monazite U-Pb and pyrite Rb-Sr isotopic dating precisely constrains the main mineralization age of the Xidouya gold deposit to 117 Ma. This timing perfectly aligns with the regional mineralization peak in the Jiaodong area, indicating the deposit formed during the Early Cretaceous extensional regime triggered by the destruction of the North China Craton.
H-O isotopic compositions suggest that the ore-forming fluids are of mixed magmatic and meteoric origin. The data trace an evolution from a magmatic water-dominated system in the early mineralization stage to a system with an increasing proportion of meteoric water input in the late stage, reflecting a mineralization process characterized by intense water–rock interaction and progressive fluid mixing in an open tectonic system.
Sulfur isotopic compositions indicate that the sulfur source of the ore-forming materials is a mixed product, dominated by crust-derived sulfur with a potential minor mantle input. The initial pyrite Rb-Sr isotopic composition further supports the hypothesis that the ore-forming materials are derived from a typical crust–mantle mixing system, which is likely related to the anatexis of ancient crust and the intense Early Cretaceous magmatic activity in the Jiaodong gold concentration area.
Author Contributions
Conceptualization, F.Z. and J.T.; methodology, J.T.; investigation, F.Z., Z.L., P.G., T.T. and D.L.; resources, Z.L.; data curation, F.Z., B.L., T.T., J.Y. and P.Z.; writing—original draft preparation, F.Z., Z.L., P.G. and T.T.; writing—review and editing, F.Z., Z.L. and J.T.; project administration, J.T.; funding acquisition, J.T. All authors have read and agreed to the published version of the manuscript.
Funding
This research was financially supported by the Shandong Provincial Natural Science Foundation, China (No. ZR2025QC426), the Open Fund of Shandong Engineering Research Center of Underground Resources and Environment High Precision Detection/Shandong Engineering Research Center of Underground Resources and Environment High Precision Detection (No. KY2025005), and the Doctoral Research Foundation of Shandong Jianzhu University (No. X21005Z).
Data Availability Statement
All data are contained within the article.
Conflicts of Interest
The authors declare no conflicts of interest.
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