Nature and origin of dolomite-hosted Th-U-HREE mineralization in the Tethyan Metallogenic Belt, Biga Peninsula, Northwestern Türkiye

• Th-U-REE mineralization occurs along fault zones in the Arıklı district, Biga Peninsula. • Cheralite in dolomite-hosted Th-U-HREE mineralization is enriched in HREE. • Dolomite-hosted Th-U-HREE mineralization formed during Early Miocene hydrothermal activity. The Biga Peninsula in northwestern Türkiye, a metallogenic province in the Tethyan Metallogenic Belt, hosts economically significant gold-copper deposits and thorium-uranium-rare earth elements (Th-U-REE) occurrences, including both light REE (LREE) and heavy REE (HREE) styles of mineralization. This contribution focuses on the nature and origins of Th-U-REE mineralization in the Arıklı district, Biga Peninsula, where three zones of Th-U-REE mineralization (A, B, and C) each extends only a few meters along faults in Cenozoic volcanic rocks. Zones A and C of U-Th-LREE mineralization are hosted by fluorapatite-sulfide-hematite and dolomite-fluorapatite assemblages and have U-Th-REE concentrations up to 1,152 ppm and 2,221 ppm, respectively, with fluorapatite as the principal U-Th-REE-bearing mineral. In contrast, Zone B of Th-U-HREE mineralization is hosted by a dolomite-dominant assemblage, with Th, U, and total HREE + Y concentrations up to 25,600 ppm, 4,100 ppm, and 3,535 ppm, respectively, with cheralite (CaTh(PO 4 ) 2 ) as the principal ore mineral. Four stages of dolomite have been identified in the main mineralization Zone B: fine to medium-crystalline dolomite (D1; anhedral), pervasive medium-grained dolomite (D2; subhedral to anhedral), dolomite rhombs (D3), and void-/vein-filling coarse-crystalline dolomite (D4). Two stages of void-/vein-filling cheralite coincide with dolomite D3 and D4. The first stage cheralite shows intense hydrothermal modification, resulting in a disturbed U-Th-Pb isotopic system. Secondary cheralite of minimal hydrothermal disturbance yielded 206 Pb- 238 U age of 18.8 ± 1.6 Ma (2σ, MSWD = 1.3) and 208 Pb- 232 Th age of 18.15 ± 0.08 Ma (2σ, MSWD = 2.3). Carbon and oxygen isotope compositions differ significantly from those of primary igneous carbonatites but are close to sedimentary rocks, indicating that all dolomites have a hydrothermal origin with sedimentary sources. These results collectively suggest that Early Miocene hydrothermal fluids most likely originated from mantle-derived alkaline magmatism and interacted with carbonate sedimentary rocks, facilitating the mobilization, enrichment, and precipitation of dolomite-hosted Th, U, and HREE mineralization in fault zones.

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Journal
Ore Geology Reviews
Published
2025-05-09
DOI
https://doi.org/10.1016/j.oregeorev.2025.106671
Citations
1
Primary Topic
Geological and Geochemical Analysis
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article
Field-Weighted Citation Impact
1.87

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article

Nature and origin of dolomite-hosted Th-U-HREE mineralization in the Tethyan Metallogenic Belt, Biga Peninsula, Northwestern Türkiye

Zhenbing She, Reza Deevsalar, Yuzhou Feng, Kenan Cao et al.
1 citations
Ore Geology Reviews
Geological and Geochemical Analysis
1.87
article

Nature and origin of dolomite-hosted Th-U-HREE mineralization in the Tethyan Metallogenic Belt, Biga Peninsula, Northwestern Türkiye

Zhenbing She, Reza Deevsalar, Yuzhou Feng, Kenan Cao, Ayetullah Tunc, Yu-Xiang Zhu, Yuanming Pan
article en
1 citations

Abstract

• Th-U-REE mineralization occurs along fault zones in the Arıklı district, Biga Peninsula. • Cheralite in dolomite-hosted Th-U-HREE mineralization is enriched in HREE. • Dolomite-hosted Th-U-HREE mineralization formed during Early Miocene hydrothermal activity. The Biga Peninsula in northwestern Türkiye, a metallogenic province in the Tethyan Metallogenic Belt, hosts economically significant gold-copper deposits and thorium-uranium-rare earth elements (Th-U-REE) occurrences, including both light REE (LREE) and heavy REE (HREE) styles of mineralization. This contribution focuses on the nature and origins of Th-U-REE mineralization in the Arıklı district, Biga Peninsula, where three zones of Th-U-REE mineralization (A, B, and C) each extends only a few meters along faults in Cenozoic volcanic rocks. Zones A and C of U-Th-LREE mineralization are hosted by fluorapatite-sulfide-hematite and dolomite-fluorapatite assemblages and have U-Th-REE concentrations up to 1,152 ppm and 2,221 ppm, respectively, with fluorapatite as the principal U-Th-REE-bearing mineral. In contrast, Zone B of Th-U-HREE mineralization is hosted by a dolomite-dominant assemblage, with Th, U, and total HREE + Y concentrations up to 25,600 ppm, 4,100 ppm, and 3,535 ppm, respectively, with cheralite (CaTh(PO 4 ) 2 ) as the principal ore mineral. Four stages of dolomite have been identified in the main mineralization Zone B: fine to medium-crystalline dolomite (D1; anhedral), pervasive medium-grained dolomite (D2; subhedral to anhedral), dolomite rhombs (D3), and void-/vein-filling coarse-crystalline dolomite (D4). Two stages of void-/vein-filling cheralite coincide with dolomite D3 and D4. The first stage cheralite shows intense hydrothermal modification, resulting in a disturbed U-Th-Pb isotopic system. Secondary cheralite of minimal hydrothermal disturbance yielded 206 Pb- 238 U age of 18.8 ± 1.6 Ma (2σ, MSWD = 1.3) and 208 Pb- 232 Th age of 18.15 ± 0.08 Ma (2σ, MSWD = 2.3). Carbon and oxygen isotope compositions differ significantly from those of primary igneous carbonatites but are close to sedimentary rocks, indicating that all dolomites have a hydrothermal origin with sedimentary sources. These results collectively suggest that Early Miocene hydrothermal fluids most likely originated from mantle-derived alkaline magmatism and interacted with carbonate sedimentary rocks, facilitating the mobilization, enrichment, and precipitation of dolomite-hosted Th, U, and HREE mineralization in fault zones.

Ore Geology ReviewsVol. 182
China University of Geosciences (CN), University of Saskatchewan (CA)
University of Saskatchewan, Natural Sciences and Engineering Research Council of Canada
Life below water
Openalex Percentile: Top 19%
Geological and Geochemical Analysis
1.87
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