Tracing Deep Carbon Cycling by Zinc Isotopes in a Peralkaline‐Carbonatite Suite

Author:

Wei Bowen123,Zhang Zhaochong2ORCID,Cheng Zhiguo2ORCID,Xie Qiuhong4,Santosh M.25ORCID,Kong Weiliang6,Liu Bingxiang7,Reichow Marc K.8,Li Yingjie1ORCID

Affiliation:

1. Hebei Province Collaborative Innovation Center for Strategic Critical Mineral Research Hebei GEO University Shijiazhuang China

2. State Key Laboratory of Geological Processes and Mineral Resources China University of Geosciences Beijing China

3. College of Earth Sciences Hebei GEO University Shijiazhuang China

4. Laboratory of Isotope Geology Institute of Geology Chinese Academy of Geological Sciences Beijing China

5. Department of Earth Sciences University of Adelaide Adelaide SA Australia

6. PetroChina Research Institute of Petroleum Exploration and Development Beijing China

7. Geological Publishing House Beijing China

8. School of Geography Geology and the Environment University of Leicester Leicester UK

Abstract

AbstractSedimentary 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.

Publisher

American Geophysical Union (AGU)

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