The Zhangquanzhuang gold deposit is a special deposit in the Zhangjiakou district, on the northern margin of the North China Craton. It is characterized by the enrichment of sulfides, the scarcity of tellurides and zero to positive sulfur isotope compositions compared with the famous Dongping and Xiaoyingpan Te-Au-Ag deposit types of the same district. In this paper, we use the in-situ LA-(MC)-ICP-MS and bulk trace element concentrations of pyrite, and in-situ sulfur isotope compositions of sulfides, to study physicochemical conditions and mechanisms of mineral deposition in the Zhangquanzhuang deposit. Pyrite from stage I (PyI) contains high Te contents, pyrite from stage II (PyII) has the highest Co and Ni contents, and pyrite from stage III (PyIII) contains high Cr, Zn, Pb, Ag, Cu, Sb, Bi and Au contents. The calculated in-situ δ³⁴S_H2S values range from 0.9‰ to 6.1‰, and the values for stages I and II are higher than those for stage III. The mineral assemblages and trace element contents in pyrite show that large amounts of metals precipitated during stage III, in which the pH and logfO₂ were constrained within the range of 4.1 to 5.2 and −36.9 to −32.1, respectively. Sulfidation and boiling derived from decreasing pressure may be the main mechanisms leading to mineral deposition in stage III. The Zhangquanzhuang gold deposit was formed in a mineral system that was different from the one that formed the Dongping and Xiaoyingpan Te-Au-Ag deposits, and should thus be called the “Zhangquanzhuang−type” deposit and considered a third gold deposit type in the Zhangjiakou ore field.

The specific source of ancient sedimentary manganese (Mn) deposits is commonly complex. Here we use systematic major and trace element data with strontium (Sr) and neodymium (Nd) isotopic analyses of the Ortokarnash Mn(II) carbonate ores and associated carbonate rocks from the Upper Carboniferous Kalaatehe Formation (ca. 320 Ma) in order to constrain the Mn source. This formation consists of three members: the first member is a volcanic breccia limestone, the second member is a sandy limestone, and the third member is a black marlstone with the Mn(II) carbonate interlayers. Petrographic observations in combination with low Al₂O₃ (<3.0 wt%) and Hf (<0.40 ppm) contents and the lack of correlations between the Al₂O₃ and ⁸⁷Sr/⁸⁶Sr ratios as well as εNd(t) values demonstrate a negligible influence of terrigenous detrital contamination on both Sr and Nd isotopic compositions of the Mn(II) carbonate ores. The Sr isotopes of Mn(II) carbonate ores are most likely affected by post-depositional alteration, while Nd isotopes remain unaltered. The initial ⁸⁷Sr/⁸⁶Sr ratios in the associated carbonate rocks are likely the result of a mixture of the chemical components (i.e., seawater) and the Al-rich components (e.g., volcanoclastic material), while the detrital effects on Nd isotopes are negligible. In addition, both Sr and Nd isotopes in these non-mineralized wall rocks remained unchanged during post-depositional processes. The relatively low Th/Sc ratios and positive εNd(t) values suggest that the aluminosilicate fraction in the calcarenite and sandy limestone was mainly derived from the weathering of a depleted mafic source, representing the riverine input into the seawater. Given that the Mn(II) carbonate ores are characterized by negative εNd(t) values, these suggest that seafloor-vented hydrothermal fluids derived from interaction with the underlying old continental crust mainly contribute to the source of the Mn(II) carbonates.

The Changkeng–Fuwan Au-Ag deposit is representative in South China, which is located in the southwest of the Qin–Hang metallogenic belt (QHMB). The Au and Ag orebodies are located in the same altered fracture zone, forming independent gold and silver orebodies respectively, with the characteristics of “upper gold and lower silver” in space. Three metallogenic stages have been identified: the pyrite–quartz–sericite stage, the polymetallic sulfide stage, and the quartz–calcite stage. The fluid inclusions (FIs) from the deposit are the two-phase liquid-rich (type I) and the pure liquid FIs (type II). The microthermometric measurements of type I FIs are characterized by temperatures of 158–282 °C and 146–289 °C and salinities of 0.35–9.88 wt.% NaCl equiv. and 0.18–11.70 wt.% NaCl equiv. The H, O, He, and Ar isotopic data show that the ore-forming fluids of the deposit were derived from a mixture of magmatic and meteoric fluids. The C and O isotopic data suggest that the carbon of the fluid may derive from a magmatic source. The S and Pb isotopic data indicate that the primary source of the metals in the Changkeng–Fuwan deposit may be a magma source. Based on the geological characteristics, FI microthermometry, and isotope data (C, H, O, He, Ar, S, and Pb), we propose that the Changkeng–Fuwan deposit should be classified as a far-source low-temperature magmatic–hydrothermal deposit.