Sedimentary carbonates are known to be carried into the deep mantle by subducted slabs, and studies on mantle‐derived magmas have attempted to trace the recycled carbonate in their mantle source. However, the final depth of storage of recycled carbonate and the role of recycled carbonate in the partial melting of mantle remain controversial. Peralkaline‐carbonatite suites are considered to have been derived from a carbonated mantle source and are windows to evaluate carbon in the mantle. In this study, we report the Zn isotopic compositions of a peralkaline‐carbonatite suite from the Tarim Large Igneous Province (Tarim LIP). The peralkaline‐carbonatite suite has heavier δ⁶⁶Zn than normal mantle with δ⁶⁶Zn of 0.34–0.40 ‰ for nephelinite, 0.35–0.47 ‰ for aillikite, 0.51–0.55 ‰ for nepheline syenite, 0.58–0.67 ‰ for calciocarbonatite and 0.38–0.56 ‰ for magnesiocarbonatite. The heavy Zn isotopic compositions of the peralkaline‐carbonatite suite in the Wajilitag complex suggest the incorporation of recycled carbonate‐bearing materials into the deep mantle. We infer that the calciocarbonatite was produced by the initial partial melting of subducted MgSiO₃/MgO + C‐bearing carbonated eclogite, whereas the magnesiocarbonatite, aillikite, and nephelinite are considered as reacted melts between carbonated eclogite‐derived melts and peridotite. The heavy Zn isotopic compositions of the nepheline syenite are attributed to fractional crystallization from nephelinite magma in the magma reservoir. Our study highlights the incorporation of carbonated eclogite as an important agent of recycled carbon in the deep mantle and interactions between carbonated eclogite‐derived melts and peridotite lead to the complex lithological heterogeneities in the peralkaline‐carbonatite suite in Tarim LIP.

Abundant Early Cretaceous magmatism is conserved in the central and southern Great Xing’an Range (GXR) and has significant geodynamic implications for the study of the Late Mesozoic tectonic framework of northeast China. In this study, we provide new high-precision U–Pb zircon geochronology, whole-rock geochemistry, and zircon Hf isotopic data for representative intrusive rocks from the northern part of the Ulanhot area to illustrate the petrogenesis types and magma source of these rocks and evaluate the tectonic setting of the central-southern GXR. Laser ablation inductively coupled plasma–mass spectrometry (LA-ICP-MS) zircon U–Pb dating showed that magmatism in the Ulanhot area (monzonite porphyry: 128.07 ± 0.62 Ma, quartz monzonite porphyry: 127.47 ± 0.36, quartz porphyry: 124.85 ± 0.34, and granite porphyry: 124.15 ± 0.31 Ma) occurred during the Early Cretaceous. Geochemically, monzonite porphyry belongs to the metaluminous and alkaline series rocks and is characterized by high Al₂O₃ (average 17.74 wt.%) and TiO₂ (average 0.88 wt.%) and low Ni (average 4.63 ppm), Cr (average 6.69 ppm), Mg^# (average 31.11), Y (average 15.16 ppm), and Yb (average 1.62 ppm) content with enrichment in Ba, K, Pb, Sr, Zr, and Hf and depletion in Ti, Nb, and Ta. The granitic rocks (e.g., quartz monzonite porphyry, quartz porphyry, and granite porphyry) pertain to the category of high-K calc-alkaline rocks and are characterized by high SiO₂ content (>66 wt.%) and low MgO (average 0.69 wt.%), Mg^# (average 31.49 ppm), Ni (average 2.78 ppm), and Cr (average 8.10 ppm) content, showing an affinity to I-type granite accompanied by Nb, Ta, P, and Ti depletion and negative Eu anomalies (δEu = 0.57–0.96; average 0.82). The Hf isotopic data suggest that these rocks were the product of the partial melting of juvenile crustal rocks. Notably, fractionation crystallization plays a crucial role in the process of magma emplacement. Combining our study with published ones, we proposed that the Early Cretaceous intrusive rocks in the Ulanhot area were formed in an extensional tectonic background and compactly related to the subduction of the Paleo-Pacific Ocean plate.

Intra-oceanic subduction is a fundamental process on Earth, the study of which can improve the understanding of plate tectonic processes and the history of continental growth. Here, we report on newly recognized trondhjemite in the north of Diyanmiao ophiolite belt in North China. The trondhjemite was found along the Erenhot-Hegenshan suture zone. U-Pb zircon dating revealed that the trondhjemite crystallized at 309 ± 2.1 Ma. The trondhjemite had a high amount of SiO₂ (68.94–76.45 wt %), Al₂O₃ (13.37–15.90 wt %), and Sr (232–601 ppm); and a low amount of K₂O (1.57–2.70 wt %), Y (6.91–9.39 ppm), Ni (1.10–4.19 ppm), and Cr (1.55–13.50 ppm). The Na₂O/K₂O ratios were 1.90–4.37. There was a lack of negative Eu anomalies. It was relatively enriched in large-ion lithophile elements (LILEs) such as Rb, Ba, K, and Sr; was depleted in high-field-strength elements (HFSEs) such as Nb, Ta, Ti, and P; and had low total rare-earth element (REE) contents (27.73–49.63 ppm) with distinct REE fractionation (chondrite-normalized (La/Yb)_N of 5.76–10.52), which was similar to adakitic rocks formed by partial melting of subducted oceanic crust. The trondhjemite, together with Diyanmiao ophiolite (335.6 Ma), may have formed during the stages of intra-oceanic subduction, suggesting that in the Early Carboniferous–Late Carboniferous, the southern Paleo-Asian Ocean was in its subduction stage.