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.

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.