Mass alkaline magmatic activities in Western Shandong during the late Mesozoic controlled the mineralization processes of gold and rare earth element (REE) polymetallic deposits in the region. The Chishan alkaline complex is closely associated with the mineralization of the Chishan REE deposit, which, as the third largest light REE deposit in China following the Baiyenebo (Inner Mongolia) and Mianning (Sichuan) deposits, is considered a typical example of alkaline rock mineralization throughout the North China Craton. To determine how the Chishan alkaline complex and REE deposit interact with each other, a systematic study was conducted on the petrology, rock geochemistry, zircon U–Pb geochronology, Lu–Hf isotopes of the quartz syenite, and alkali granite contained in the Chishan alkaline complex. The results reveal that the deposits feature similar geochemical characteristics typical of an alkaline rock series—both are rich in alkali, high in potassium, metaluminous, and poor in Ti, Fe, Mg, and Mn. In terms of REEs, the deposits are strongly rich in light REEs but poor in heavy REEs, with weak negative Eu anomalies. In terms of trace elements, they are rich in large ion lithophile elements Ba, Sr, and Rb but poor in high field-strength elements Nb, Ta, and Hf. Zircon LA-ICP-MS U–Pb dating indicated that the quartz syenite and alkali granite formed in Early Cretaceous at 125.8 ± 1.2 Ma and 127.3 ± 1.0 Ma, respectively; their εHf(t) values are −22.67 to −13.19, with depleted model ages (T_DM) ranging from 1296 Ma to 1675 Ma and crustal model ages (T_DM^C) of 2036–2617 Ma. The Chishan alkaline complex originated from partial of the EM I-type (enriched mantle I) lithospheric mantle with assimilation of ancient crustal materials. The complex is of the same origin as the REE deposit, and developed in an extensional setting that resulted from plate subduction and lithospheric thinning and upwelling in the eastern area of the North China Craton.

The Houge’zhuang gold deposit, located in the Penglai–Qixia gold belt of the Jiaodong peninsula, is a representative auriferous quartz vein-style deposit. Pyrite is the most common and main gold-bearing mineral and shows complex textures in the Houge’zhuang gold deposit. Study of ore-related pyrite is of great significance for understanding the metallogenesis of this deposit, especially the gold precipitation mechanism. The present study applied systematic microscopic observation, fluid inclusion analysis, electron microprobes,in situ LA-ICP-MS trace-element analysis, and in situ sulfur isotope analyses. Three types of fluid inclusions were identified, among which the ore-forming fluids exhibited medium–low salinity and temperature, with the fluid inclusions mainly comprising H₂O and CO₂. Three types of pyrites were identified: 1) Py0, characterized by low concentrations of As and Au and low δ³⁴S values (5.51–6.86‰). 2) Py1, found in the gold-quartz-pyrite veins and homogeneous in chemical composition with no obvious zonal growth but with notably more gold and chalcopyrite inclusions. Py1 contained medium and uniform concentrations of As and was Au-rich, with δ³⁴S values ranging from 7.13 to 7.89‰ (mean 7.44‰). 3) Py2 contained arsenic-bearing pyrite and was found in quartz-polymetallic sulfide veins, with distinct As enrichment and As-rich rims of pyrite and growth zoning. Consequently, the primary ore-forming fluids passed through some arsenic and δ³⁴S-rich sedimentary rocks, such as the Jingshan, Fenzishan, and Penglai groups. With the occurrence of stable water-rock interaction, the extracted fluids were enriched for As and δ³⁴S. Furthermore, Au was closely associated with As, visible gold grains tended to occur in association with Py1 at stage II, and invisible gold was related to the Au-As-rich Py2 of stage III. The As-bearing pyrites shared a close spatiotemporal relationship with gold, playing an important role in the formation and exploration of high-grade gold deposits.

The Jiaodong Peninsula is the most important gold mineralization area in China, and the formation of gold deposits is closely related to granitoids. The isotopic ages of the Early Cretaceous granodiorites in the northwestern Jiaodong Peninsula are concentrated in the range of 111~123 Ma, and are coeval with the formation of the gold deposits in the area. However, the studies on the geotectonic settings of the granodiorites, especially their petrogenesis and relationship with gold deposits in the northwestern Jiaodong Peninsula, are scarce. Based on field and petrographic observations, geochemistry, EPMA analysis, zircon U-Pb chronology, and Sr-Nd isotopes of the Early Cretaceous Zhouguan granodiorite in the Jiaodong area, the formation age of Zhouguan granodiorite is determined as 115 Ma ± 0.77 Ma; the analysis of EPMA shows that biotite is mainly composed of Fe-biotite and Mg-biotite, with its MgO content ranging from 9.797% to 11.635%. The crystallization temperature of biotite is in the range of 500 °C~625 °C and the emplacement depth of the rock mass is 3.98~8.71 km. The amphibole in the mass mainly includes magnesiohornblende, pargasite, and magnesiosadanagaite; among them, the former two are of crustal origin, while magnesiosadanagaite is of mantle origin. The crystallization pressure and depth of the former two are in the range of 0.75~3.02 kbar and 2.81~11.4 km, respectively, while the crystallization pressure and depth for the latter is 4.64 kbar and 17.53 km, respectively. The (⁸⁷Sr/⁸⁶Sr) values range from 0.710424 to 0.711074 and the (¹⁴³Nd/¹⁴⁴Nd) values range from 0.511530 to 0.511808. The parental magma of the Zhouguan granodiorite is highly oxidized with high-water content that is favorable for Au enrichment. Combined with the Nb-Y and Yb-Ta diagrams, a model describing the formation of Zhouguan granodiorite is proposed.

With a focus on the Cu isotope geochemistry of chalcopyrite, this paper analyzed the Cu isotope geochemistry of the Qibaoshan crypto-explosive breccia-type Cu–Au polymetallic ore district in Wulian, Shandong Province, North China Craton (NCC). Combined with the results of the in situ sulfur isotope analysis of sulfides, a certain reference and evidence for the study of the genetic mechanism of the epithermal-porphyry Cu polymetallic metallogenic system were provided. The results of the in situ isotope analysis show that the δ³⁴S values of the main sulfides in the Qibaoshan Cu–Au polymetallic ore district range from −6.81‰ to +3.82‰ and are likely to be attributed to the mixing of the derived mantle with the surrounding sedimentary rock assimilation. The ore-forming mechanism may be related to the progressive cooling and transition of the earliest hydrothermal fluids that were dominated by H₂S under relatively reducing conditions, followed by a gradual transition from oxidation to reduction. The Cu isotopic composition of the sulfides in ores (δ⁶⁵Cu = +0.169‰–+0.357‰) decreases with depth, which is likely caused by the upward transport of heavier Cu isotopes. The upper part of the crypto-explosive breccia pipe in the Qibaoshan area may be relatively more gaseous, resulting in the enrichment of δ⁶⁵Cu. As the gas phase decreases and the liquid phase increases with depth, the δ⁶⁵Cu value gradually decreases. This indicates the transition from a low-temperature phyllic alteration to a high-temperature K-feldspar alteration. Large, concealed pluton intrusions or orebodies may be present at a depth of the Qibaoshan area. The heavy δ⁶⁵Cu characteristic is a potential indicator for tracing the fluid activity of the porphyry system and searching for Cu mines. The results provide a reference for the study of the genetic mechanisms of the epithermal-porphyry Cu polymetallic metallogenic system.