Journal of Tropical Oceanography ›› 2026, Vol. 45 ›› Issue (5): 146-161.doi: 10.11978/YG2026001CSTR: 32234.14.YG2026001

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Controlling factors and implications of magnesium isotopic compositions of marine carbonates*

HUANG Kangjun1(), ZHANG Pan1, FENG Dong2, YAN Wen3   

  1. 1 Department of Geology, State Key Laboratory of Continental Evolution and Early Life, Shanxi Key Laboratory of Early Life and Environment, Northwest University, Xi’an 710069, China
    2 College of Ocean and Ecological Sciences, Shanghai Ocean University, Shanghai 201306, China
    3 Key Laboratory of Marginal Sea Geology (South China Sea Institute of Oceanology), South China Sea Ecology and Environment Engineering Innovation Research Institute, Chinese Academy of Sciences, Guangzhou 510301, China
  • Received:2026-02-11 Revised:2026-03-04 Online:2026-09-10 Published:2026-10-13
  • Contact: HUANG Kangjun. email: hkj@nwu.edu.cn
  • Supported by:
    National Key Research and Development Program of China(2021YFC3100600); Key Laboratory of Ocean and Marginal Sea Geology, Chinese Academy of Sciences(OMG2020—02)

Abstract:

The magnesium isotope composition (δ26Mg) of shallow-water carbonates provides critical constraints on the marine Mg cycle, paleoclimate, and diagenesis. However, the impact of meteoric and mixing-zone diagenesis on carbonate δ26Mg remains poorly understood, and these diagenetic effects exhibit significant regional variability. Here, we investigate how mineralogy (aragonite, calcite, and dolomite) and diagenetic environments (meteoric, marine, mixing-zone diagenesis, and dolomitization) influence bulk carbonate δ26Mg, integrating mineralogical and geochemical analyses with numerical modeling using samples from Well NK-1 (Meiji Atoll, South China Sea). Results indicate that carbonate δ26Mg is co-controlled by mineral composition and the diagenetic environment. Fluid-buffered dolomites and well-preserved high-Mg calcites exhibit fractionation offsets of ~ −2.0‰ and ~ −2.4‰ relative to coeval seawater, respectively, making them reliable archives for seawater δ26Mg reconstruction. In contrast, aragonite-dominated samples are highly susceptible to alteration by secondary calcite due to the low Mg content of aragonite. Furthermore, calcite δ26Mg varies widely (−5.1‰ to −3.1‰), corresponding to isotope fractionation factors between −4.5‰ and −4.0‰ during meteoric, mixing-zone, and marine diagenesis. This suggests that aragonite and low-Mg calcite are poor archives of seawater δ26Mg, whereas the least-altered limestone samples may constrain the lower limit of coeval seawater δ26Mg (offset ~ −2.4‰). Global comparisons indicate that limestone δ26Mg variability is primarily controlled by the diagenetic setting and the degree of alteration. This study underscores the importance of evaluating diagenetic alteration to assess the fidelity of seawater chemistry records, refines our understanding of Mg isotope behavior during diagenesis, and clarifies the key controls on global carbonate δ26Mg.

Key words: Meiji Atoll, Well NK-1, recrystallization, calcite, meteoric diagenesis

CLC Number: 

  • P734.24