Several small chromium (Cr) ore bodies are hosted within a unit of tectonically thinned dunite in the retired Ayios Stefanos mine of the western Othris ophiolite complex in Greece. Chromium ores consist of tectonically imprinted bodies of semi-massive to massive, podiform and lenticular chromitites composed of chromian spinel [Cr-spinel] and mid-ocean ridge basalts (MORBs). Several Cr-spinel crystals in these ores exhibit imperfect zones made up of spinel hosting oriented lamellae of Mg-silicates (mostly chlorite) locally overgrown by porous domains along grain boundaries and fractures. From the Cr-spinel core to the lamellae-rich rim Cr#, Mg# and Fe 3+ # generally increase (0.68-0.87, 0.78-0.88 and 0.55-0.80, respectively), whereas from the core or the spinel zones with oriented lamellae to the porous domains Mg# and Fe 3+ # generally decrease (0.45-0.74 and ≤0.51, correspondingly). The lamellae-rich rims formed at oxidizing conditions, whereas the porous rims resulted from a later reducing event. Several tiny (≤30 µm), subhedral to anhedral and elongated Zr-bearing silicate mineral grains were discovered mainly along open and healed fractures cutting Cr-spinel. Most of the Zr-bearing silicate minerals (30 out of 35 grains) were found in a chromitite boulder vastly intruded by a complex network of gabbroic dykes. The dominant Zr-bearing silicate phase is by far zircon displaying a homogeneous internal texture in cathodoluminescence (CL) images. Raman spectroscopy data indicate that zircons have experienced structural damage due to self-irradiation. Their trace-element contents suggest derivation from a plagioclase-bearing, low-SiO 2 intermediate to mafic source. Combined micro-textural and minerochemical data repeat the possibility of zircon derivation from limited volumes of high-T fluids emanating from the gabbroic intrusions. Once zircon is precipitated in cracks, it may be altered to Ca-rich Zr-bearing silicate phases (i.e., armstrongite, calciocatapleiite). Almost all zircons in these samples show evidence of gains in solvent compounds (CaO, Al 2 O 3 and FeO) possibly due to re-equilibration with late deuteric fluids.