The Chromite Crisis in the Evolution of Continental Magmas and the Initial High δ26Mg Reservoir

Author:

Xiao Yan1,Yuan Meng12,Su Ben-Xun23,Chen Chen4,Bai Yang5,Ke Shan6,Sun Yang7,Robinson Paul T1

Affiliation:

1. Chinese Academy of Sciences State Key Laboratory of Lithospheric Evolution, Institute of Geology and Geophysics, , Beijing 100029, China

2. University of Chinese Academy of Sciences , Beijing 100049, China

3. Chinese Academy of Sciences Key Laboratory of Mineral Resources, Institute of Geology and Geophysics, , Beijing 100029, China

4. Chinese Academy of Sciences Key Laboratory of Mineralogy and Metallogeny, Guangzhou Institute of Geochemistry, , Guangzhou 510640, China

5. College of Mining Engineering Taiyuan University of Technology, , Taiyuan 030024, China

6. China University of Geosciences State Key Laboratory of Geological Processes and Mineral Resources, , Beijing 100083, China

7. Southern University of Science and Technology Department of Earth and Space Sciences, , Shenzhen 518055, Guangdong, China

Abstract

Abstract Fractional crystallization of Fe–Ti oxides can induce detectable Mg isotopic changes during late-stage basalt differentiation. Because chromite and olivine are early crystallizing phases during basaltic melt differentiation, the effect of chromite crystallization on the fractionation of Mg isotopes during early-stage basalt differentiation is still poorly understood. Here, we examine the possibility of chromite induced Mg isotope fractionation with a Mg isotopic study of chromite–olivine pairs in dunites and chromitites collected from major types of basaltic intrusive rock suites formed by fractional crystallization in different tectonic settings. The chromite δ26Mg (= [(26Mg/24Mg)sample / (26Mg/24Mg)DSM3–1] × 1000) values range from −0.19‰ to 0.30‰ in the Luobusa ophiolite, −0.09‰ to 0.78‰ in the Kızıldağ ophiolite, −0.04 to 0.42‰ in the Gaositai Alaskan-type complex, similar to those previously reported from the Stillwater layered intrusion (−0.05 to 0.84‰; Bai et al., 2021). They are significantly higher than those of coexisting olivine (δ26Mg = −0.48 to −0.10‰). The Δ26MgChr-Ol (= δ26MgChr − δ26MgOl) values in the rock suites investigated here fall largely between equilibrium fractionation lines of spinel–olivine pairs and magnesioferrite–olivine pairs, indicating equilibrium Mg isotopic fractionation. Furthermore, the Δ26MgChr-Ol values increase with decreasing Cr content of chromite in the dunites and chromitites, showing that high 26Mg has a greater affinity to Al-rich chromite than Cr-rich chromite. Fractional crystallization of such isotopically high chromite is expected to progressively lower the Mg isotope values of the in the remaining magma. Furthermore, continental basaltic magmas typically experience early crystallization of olivine and Al-rich chromite. Their δ26Mg values correlate positively with MgO (FeO, Cr,) and CaO/Al2O3 ratios and negatively with total alkali contents (Na2O + K2O). This indicates that detectable Mg isotopic fractionation occurred in intra-continental basalt magmas, probably by fractional crystallization of olivine and chromite. The observed low-δ26Mg intra-continental basalts can be accurately modeled by olivine + chromite fractionation with fractionation factors (Δ26MgChr-Melt) of 0.20‰, 0.60‰, and 1.18‰ as observed in the chromitites investigated during this study. Therefore, the early-stage basaltic melt differentiation involving separation of olivine and chromite may induce resolvable Mg isotopic fractionation, and the δ26Mg values of continental basalts should be used with caution in petrogenetic studies.

Publisher

Oxford University Press (OUP)

Subject

Geochemistry and Petrology,Geophysics

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