Chromitites associated with rodingite from the Deva mining district (Mirdita Ophiolite, Kosovo) display thick reaction rims at the contact between chromite and silicate matrix. The most peculiar feature of these rims is an anomalous enrichment in titanium (Ti) and vanadium (V) in the chromite, alongside the presence of abundant rutile, ilmenite and titanite. The integration of textural and mineralogical observations, minero-chemical data and statistical analysis, through Principal Component Analysis (PCA), reveals a complex evolution of the chromitite body and its host rocks. Primary chromitites formed in a supra-subduction zone forearc environment, from melts with boninitic affinity. The subsequent intrusion of a mafic body and its interaction with the chromitites led to significant enrichments in Ti, V and minor Ga, Ni and Mn in chromite. At lower temperature, Ti was partially exsolved to form Ti-phases. During a later serpentinization event affecting the ophiolite mantle rocks, the circulation of reducing hydrothermal fluids caused the rodingitization of the mafic intrusion, replacing primary silicates with hydrogrossular, clinopyroxene and chlorite. While serpentinization and rodingitization only marginally affected the chromitite body, they caused local Al re-enrichment in the previously depleted spinel rims due to the liberation of Aluminum during plagioclase break-up. The study highlights the complexity of superimposed magmatic and low-temperature processes capable of modifying chromite chemistry and emphasizes the importance of integrated approaches in unraveling their individual contributions.

Melt-rock interaction driving extreme titanium and vanadium enrichments during the multi-stage post-magmatic evolution of chromite from the Mirdita Ophiolite, Kosovo / M. Bussolesi, G. Grieco, A. Cavallo, Q. Hyseni, F. Farina. - In: LITHOS. - ISSN 0024-4937. - 534-535:(2026 Aug), pp. 108546.1-108546.14. [10.1016/j.lithos.2026.108546]

Melt-rock interaction driving extreme titanium and vanadium enrichments during the multi-stage post-magmatic evolution of chromite from the Mirdita Ophiolite, Kosovo

M. Bussolesi
Primo
;
G. Grieco;A. Cavallo;F. Farina
Ultimo
2026

Abstract

Chromitites associated with rodingite from the Deva mining district (Mirdita Ophiolite, Kosovo) display thick reaction rims at the contact between chromite and silicate matrix. The most peculiar feature of these rims is an anomalous enrichment in titanium (Ti) and vanadium (V) in the chromite, alongside the presence of abundant rutile, ilmenite and titanite. The integration of textural and mineralogical observations, minero-chemical data and statistical analysis, through Principal Component Analysis (PCA), reveals a complex evolution of the chromitite body and its host rocks. Primary chromitites formed in a supra-subduction zone forearc environment, from melts with boninitic affinity. The subsequent intrusion of a mafic body and its interaction with the chromitites led to significant enrichments in Ti, V and minor Ga, Ni and Mn in chromite. At lower temperature, Ti was partially exsolved to form Ti-phases. During a later serpentinization event affecting the ophiolite mantle rocks, the circulation of reducing hydrothermal fluids caused the rodingitization of the mafic intrusion, replacing primary silicates with hydrogrossular, clinopyroxene and chlorite. While serpentinization and rodingitization only marginally affected the chromitite body, they caused local Al re-enrichment in the previously depleted spinel rims due to the liberation of Aluminum during plagioclase break-up. The study highlights the complexity of superimposed magmatic and low-temperature processes capable of modifying chromite chemistry and emphasizes the importance of integrated approaches in unraveling their individual contributions.
Mediterranean ophiolite; Melt-rock reaction; PCA; Rodingite; Ti- V-rich chromite
Settore GEOS-01/D - Georisorse minerarie e applicazioni mineralogico-petrografiche per l'ambiente e per i beni culturali
Settore GEOS-01/C - Geochimica e vulcanologia
ago-2026
7-apr-2026
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1239835
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