In situ elemental and Sr-Nd isotopic compositions of hydrothermal apatite from the Shazhou U deposit in the Xiangshan complex: Implications for the origins of ore-forming fluids of volcanic related U deposits in South China

The origin of ore-forming fluids of volcanic related U deposits remains controversial. This study reports in situ elemental and Sr-Nd isotopic compositions of apatite associated with U mineralization from the Shazhou volcanic related U deposit in South China, which provides a new perspective to constrain the origin and evolution of its ore-forming fluids. Hydrothermal apatites from the hematized rocks and U-mineralized rocks show distinct textures and chemical features, indicating two types of fluids involved in the U mineralization process. The hematitization fluid was oxidizing and enriched in U and Cl. A reducing fluid with lower Cl/F and U was introduced and mixed with the oxidizing hematitization fluid to cause U precipitation. Apatite from the hematized rocks has a lower ⁸⁷Sr/⁸⁶Sr (0.709246–0.714383) than that of apatite in U ore veins (0.710383–0.719318). The εNd(t) of apatite in the hematized rocks is from −7.6 to −9.4, whereas apatite in U ore veins has higher εNd(t) ranging from −1.2 to −8.4, close to that of mafic dikes intruded into the volcanic rocks. In situ Sr-Nd isotopes of apatite indicate the oxidizing fluid originated from the red-bed basins, whilst the origin of the reducing fluid was related to the mantle-derived mafic dikes. The reducing fluid has experienced assimilation by the metamorphic basement rocks to gain higher radiogenic strontium. This study demonstrates that in situ elemental and Sr-Nd isotopic compositions of apatite are effective in identifying different ore-forming hydrothermal fluids and constraining their origins and chemical evolution.