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Apatite Sr-Nd and zircon Hf-O isotopes are broadly used to trace magma sources and constrain magma evolution processes, further improving our understanding of the origin of granitoids. We present zircon U-Pb ages, whole-rock major and trace elements, and whole-rock Sr-Nd-Hf, zircon Hf-O, and apatite Sr-Nd isotopic data for the coarse-grained quartz monzonite, biotite monzogranite, and granite porphyry in the Yushulinzi pluton in the Liaodong Peninsula, the eastern North China Craton, to establish their magma sources and petrogenesis. The coarse-grained quartz monzonite, biotite monzogranite, and granite porphyry were formed contemporaneously, with zircon U-Pb ages of 123–119 Ma. They share enriched whole-rock Sr-Nd-Hf and zircon Hf isotopic compositions, and the coarse-grained quartz monzonite has crust-like δ18O values (5.7–6.7‰). The coarse-grained quartz monzonite and biotite monzogranite have variable apatite (87Sr/86Sr)i ratios and negative apatite εNd(t) values. These isotopic characteristics indicate that the different rock types in the Yushulinzi pluton were derived from the partial melting of ancient crustal material in the North China Craton. Their geochemical and petrographic characteristics indicate that the crystal-melt segregation model can be employed to elucidate the genetic links among different rock types, with the coarse-grained quartz monzonite representing crystal accumulation and the biotite monzogranite and granite porphyry representing interstitial melts extracted from a crystal-rich magma chamber. Furthermore, the variable apatite Sr isotopic compositions and subtle differences in the peak zircon εHf(t) values of the studied rock samples confirm the possibility of a contribution from shallow crustal components and materials with high εHf(t) values during magma evolution, which is not readily revealed by their whole-rock Sr-Nd-Hf isotopic compositions. These results demonstrate that in situ apatite Sr-Nd and zircon Hf-O isotopic analyses have the potential to provide distinctive insights into the magma sources and evolution of magmatic systems. [ABSTRACT FROM AUTHOR]

Apatite Sr-Nd and zircon Hf-O isotopes are broadly used to trace magma sources and constrain magma evolution processes, further improving our understanding of the origin of granitoids. We present zircon U-Pb ages, whole-rock major and trace elements, and whole-rock Sr-Nd-Hf, zircon Hf-O, and apatite Sr-Nd isotopic data for the coarse-grained quartz monzonite, biotite monzogranite, and granite porphyry in the Yushulinzi pluton in the Liaodong Peninsula, the eastern North China Craton, to establish their magma sources and petrogenesis. The coarse-grained quartz monzonite, biotite monzogranite, and granite porphyry were formed contemporaneously, with zircon U-Pb ages of 123–119 Ma. They share enriched whole-rock Sr-Nd-Hf and zircon Hf isotopic compositions, and the coarse-grained quartz monzonite has crust-like δ18O values (5.7–6.7‰). The coarse-grained quartz monzonite and biotite monzogranite have variable apatite (87Sr/86Sr)i ratios and negative apatite εNd(t) values. These isotopic characteristics indicate that the different rock types in the Yushulinzi pluton were derived from the partial melting of ancient crustal material in the North China Craton. Their geochemical and petrographic characteristics indicate that the crystal-melt segregation model can be employed to elucidate the genetic links among different rock types, with the coarse-grained quartz monzonite representing crystal accumulation and the biotite monzogranite and granite porphyry representing interstitial melts extracted from a crystal-rich magma chamber. Furthermore, the variable apatite Sr isotopic compositions and subtle differences in the peak zircon εHf(t) values of the studied rock samples confirm the possibility of a contribution from shallow crustal components and materials with high εHf(t) values during magma evolution, which is not readily revealed by their whole-rock Sr-Nd-Hf isotopic compositions. These results demonstrate that in situ apatite Sr-Nd and zircon Hf-O isotopic analyses have the potential to provide distinctive insights into the magma sources and evolution of magmatic systems.

Carbonatites and related alkaline rocks host most REE resources. Phosphate minerals, e.g., apatite and monazite, commonly occur as the main REE-host in carbonatites and have been used for tracing magmatic and mineralization processes. Many carbonatite intrusions undergo metamorphic and/or metasomatic modification after emplacement; however, the effects of such secondary events are controversial. In this study, the Miaoya and Shaxiongdong carbonatite-alkaline complexes, in the South Qinling Belt of Central China, are selected to unravel their magmatic and hydrothermal remobilization histories. Both the complexes are accompanied by Nb-REE mineralization and contain apatite and monazite-(Ce) as the major REE carriers. Apatite grains from the two complexes commonly show typical replacement textures related to fluid metasomatism, due to coupled dissolution-reprecipitation. The altered apatite domains, which contain abundant monazite-(Ce) inclusions or are locally surrounded by fine-grained monazite-(Ce), have average REE concentrations lower than primary apatite. These monazite-(Ce) inclusions and fine-grained monazite-(Ce) grains are proposed to have formed by the leaching REE from primary apatite grains during fluid metasomatism. A second type of monazite-(Ce), not spatially associated with apatite, shows porous textures and zoning under BSE imaging. Spot analyses of these monazite-(Ce) grains have variable U-Th-Pb ages of 210-410 Ma and show a peak age of 230 Ma, which is significantly younger than the emplacement age (440-430 Ma) but is roughly synchronous with a regionally metamorphic event related to the collision between the North China Craton and Yangtze Block along the Mianlue suture. However, in situ LA-MC-ICP-MS analyses of those grains show that they have initial Nd values same as those of magmatic apatite and whole rock. We suggest these monazite-(Ce) grains crystallized from the early Silurian carbonatites and have been partially or fully modified during a Triassic metamorphic event, partially resetting U-Pb ages over a wide range. Mass-balance calculations, based on mass proportions and the REE contents of monazite-(Ce) and apatite, demonstrate that the quantity of metasomatized early Silurian monazite-(Ce) is far higher than the proportion of monazite-(Ce) resulting from the metasomatic alteration of the apatite. Therefore, Triassic metamorphic events largely reset the U-Th-Pb isotopic system of the primary monazite-(Ce) and apatite but only had limited or local effects on REE remobilization in the carbonatite-alkaline complexes in the South Qinling Belt. Such scenarios may be widely applicable for other carbonatite and hydrothermal systems. [ABSTRACT FROM AUTHOR]