Abstract

Pyrite is widely distributed in the Earth’s crust and oceanic systems, and it generally occurs as pentagonal dodecahedra, cubic, octahedral, idiomorphic crystals, or dense, massive, granular, and nodular aggregates. In this study, representative pyrite samples from Hunan, Fujian, Jiangxi, Anhui in China and from Peru were collected. By utilizing a range of analytical techniques, including petrography, X-ray diffraction, infrared spectrum, Raman spectrum, major and trace element analysis, as well as sulfur stable isotope analysis, we comprehensively depict the mineralogical and spectroscopic characteristics of pyrite, and the evolution processes of the physical and chemical conditions of mineralization can be qualitatively constrained. The spectroscopic results indicate all samples show a relatively narrow absorption band with weak to moderate intensity in the vicinity of 343 cm−1, which represents the bending vibration of the Fe-[S2]2− molecular bond. The Co content of pyrite exhibits the characteristics of a positive correlation with temperature and a negative correlation with oxygen fugacity, respectively. The δ34S isotopic compositions of colloidal pyrite are in the range of 0.03 to 0.67, which are close to meteoric sulfur and mantle sulfur compositions, while the δ34S values of nodular pyrite fall within the range of granite, indicating the characteristics of mixtures of sulfur sources are mainly related to magmatic activity. Our results provide insight into the formation mechanisms of pyrite in different environments, its mineralization, and the ore genesis of deposits. Moreover, the integrated analytical methods for pyrite are provided, which can define theoretical guidance for the exploration and development of mineral resources.

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