Biotite and apatite geochemistry of granites from the Caledonian Debao Sn-Cu deposit, South China: Implications for petrogenesis and mineralization

• Biotite and apatite geochemistry indicates that the Debao granite is reduced, crust-derived granite. • Magmatic fractionation from porphyritic granite to equigranular granite is critical to Sn enrichment and mineralization. • Cu mineralization at Debao is genetically related to the S-poor, reduced, and evolved granitic magmatism. The Debao Sn-Cu skarn deposit is a rare Caledonian granite-related Sn deposit in South China. The petrogenesis of the ore-related granites and the origin of the Sn-Cu mineralization in this deposit are still unclear. In this study, we present biotite and apatite chemical compositions, as well as apatite Nd isotopic compositions from the Debao porphyritic/equigranular biotite granites to constrain the petrogenesis and their potential roles in Sn-Cu mineralization. The two types of biotite granites have similar apatite ε Nd (t) (–7.0 to –3.7) with Nd model ages (1743–1479 Ma). Combined with the relatively high apatite Y (1746–6852 ppm) and low biotite MgO (3.97–7.58 wt%) contents, the data suggest that the granites were crust-derived, including mainly Mesoproterozoic metasedimentary rocks with some Neoproterozoic arc-related rocks input. The biotite Fe 3+ –Fe 2+ –Mg discrimination plot and the low apatite SO 3 content (≤0.04 wt%) suggest low oxygen fugacity (between the FMQ and NNO buffer). Halogen (F, Cl) compositions (relatively high F and low Cl contents) in the biotite and apatite from the Debao granites resemble those of Sn deposits in South China. Biotite from the porphyritic granite has lower Li-Rb-Nb-Ta but higher Ba-V-Co-Ni contents than the equigranular granite, whilst the apatite from the porphyritic granite has lower total rare earth element (ΣREE) content than that from the equigranular granite. For zoned apatite, the ΣREE content increases from the cores to the rims. These element variations are consistent with the magma fractionation trend. The porphyritic granite has lower biotite Sn content (6.69–41.4 ppm) than that of the equigranular granite (43.6–101 ppm), suggesting that magma fractionation is critical to Sn enrichment at Debao. Given that there is no addition of mafic magma and/or its derived fluids into the crust-derived reduced magma at Debao, and that there is no Cu-rich wallrocks at Debao, we inferred that fractionation of the probable S-poor, reduced biotite granitic magmatism at Debao could generate certain Cu enrichment and small-scale hydrothermal Cu mineralization.

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Publication Details

Journal
Ore Geology Reviews
Published
2025-02-22
DOI
https://doi.org/10.1016/j.oregeorev.2025.106510
Citations
4
Primary Topic
Geological and Geochemical Analysis
Type
article
Field-Weighted Citation Impact
7.47
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article

Biotite and apatite geochemistry of granites from the Caledonian Debao Sn-Cu deposit, South China: Implications for petrogenesis and mineralization

Wenlong Huang, Yinqiao Zou, Quan Ou, Cheng Wang et al.
4 citations
Ore Geology Reviews
Geological and Geochemical Analysis
7.47
article

Biotite and apatite geochemistry of granites from the Caledonian Debao Sn-Cu deposit, South China: Implications for petrogenesis and mineralization

Wenlong Huang, Yinqiao Zou, Quan Ou, Cheng Wang, Puliang Lv, Jian Zhang
article en
4 citations

Abstract

• Biotite and apatite geochemistry indicates that the Debao granite is reduced, crust-derived granite. • Magmatic fractionation from porphyritic granite to equigranular granite is critical to Sn enrichment and mineralization. • Cu mineralization at Debao is genetically related to the S-poor, reduced, and evolved granitic magmatism. The Debao Sn-Cu skarn deposit is a rare Caledonian granite-related Sn deposit in South China. The petrogenesis of the ore-related granites and the origin of the Sn-Cu mineralization in this deposit are still unclear. In this study, we present biotite and apatite chemical compositions, as well as apatite Nd isotopic compositions from the Debao porphyritic/equigranular biotite granites to constrain the petrogenesis and their potential roles in Sn-Cu mineralization. The two types of biotite granites have similar apatite ε Nd (t) (–7.0 to –3.7) with Nd model ages (1743–1479 Ma). Combined with the relatively high apatite Y (1746–6852 ppm) and low biotite MgO (3.97–7.58 wt%) contents, the data suggest that the granites were crust-derived, including mainly Mesoproterozoic metasedimentary rocks with some Neoproterozoic arc-related rocks input. The biotite Fe 3+ –Fe 2+ –Mg discrimination plot and the low apatite SO 3 content (≤0.04 wt%) suggest low oxygen fugacity (between the FMQ and NNO buffer). Halogen (F, Cl) compositions (relatively high F and low Cl contents) in the biotite and apatite from the Debao granites resemble those of Sn deposits in South China. Biotite from the porphyritic granite has lower Li-Rb-Nb-Ta but higher Ba-V-Co-Ni contents than the equigranular granite, whilst the apatite from the porphyritic granite has lower total rare earth element (ΣREE) content than that from the equigranular granite. For zoned apatite, the ΣREE content increases from the cores to the rims. These element variations are consistent with the magma fractionation trend. The porphyritic granite has lower biotite Sn content (6.69–41.4 ppm) than that of the equigranular granite (43.6–101 ppm), suggesting that magma fractionation is critical to Sn enrichment at Debao. Given that there is no addition of mafic magma and/or its derived fluids into the crust-derived reduced magma at Debao, and that there is no Cu-rich wallrocks at Debao, we inferred that fractionation of the probable S-poor, reduced biotite granitic magmatism at Debao could generate certain Cu enrichment and small-scale hydrothermal Cu mineralization.

Ore Geology ReviewsVol. 179
Sun Yat-sen University (CN), China Geological Survey (CN), Hunan Vocational College of Safety Technology (CN), Nanning Normal University (CN), China Nonferrous Metals Changsha Investigation Design Institute (CN)
Openalex Percentile: Top 3%
Geological and Geochemical Analysis
7.47
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