A new occurrence of kintoreite, ideally PbFe3(PO4)(PO3OH)(OH)6, is described from the Tripi mine, Alì, Peloritani Mountains, northeastern Sicily, Italy. Kintoreite occurs as yellow equant crystals, up to 0.05 mm in size, on quartz, associated with another alunite-supergroup mineral currently under study. The studied grains of kintoreite are chemically zoned, showing the occurrence of two distinct domains. Electron microprobe analyses gave (in wt.%): SO3 5.47(27), P2O5 17.55(14), Al2O3 7.81(35), Fe2O3 23.81(44), PbO 35.11(41), H2Ocalc 9.93, total 99.68 (darker domains) and SO3 6.03(5), P2O5 16.66(23), Al2O3 4.22(2), Fe2O3 27.31(6), PbO 33.78(22), H2Ocalc 10.25, total 98.25 (brighter domains). On the basis of 14 O atoms per formula unit (apfu) and (P+S) = 2 apfu, the darker and brighter domains have chemical formula Pb1.00(Fe3+1.89Al0.97)Σ2.86[P1.57S0.43O7.43(OH)0.57][(OH)5.58(H2O)0.42]Σ6.00 and Pb0.98(Fe3+2.21Al0.53)Σ2.74[P1.51S0.49O7.49(OH)0.51][(OH)5.18(H2O)0.82]Σ6.00, respectively. Single-crystal X-ray diffraction was performed on a grain extracted from the same sample. Unit-cell parameters are a = 7.2191(10), c = 16.834(3) Å, V = 759.8(3) Å3 and Z = 3; space group R$\bar{3}$m. The crystal structure was refined on the basis of 226 unique reflections with Fo > 4σ(Fo) and 31 least-square parameters to R1 = 0.0415. Kintoreite is isotypic with other alunite-supergroup minerals. Micro-Raman spectroscopy suggests the possible occurrence of H2O groups, supporting the possible protonation of (OH) groups as a charge-balance mechanism in this mineral. Kintoreite may play an environmental role in the Alì area, where previous authors detected high concentrations of potentially toxic elements in soils.

The Peloritani Mountains constitute the Sicilian portion of the Calabria–Peloritani Arc (Italy), a tectono-metamorphic edifice recording the history of the subduction–exhumation cycle during Tertiary convergence between the African and European plates. Here, we describe the kinematic and the petrological characteristics of the major shear zones bounding the lowermost continental-derived metamorphic units cropping out in the eastern portion of the Peloritani Mountains. Both meso- and micro-scale shear sense criteria indicate a top-to-the-SSE tectonic transport, during a general evolution from ductile to brittle deformation conditions. Quantitative thermobarometry on texturally equilibrated phengite–chlorite pairs crystallized along the shear bands indicates pressure of 6–8 kbar at temperatures of 360–440 °C for the structurally highest units and 3–4 kbar at 380–440 °C for the lowest ones. This documents an overall inverse-type nappe arrangement within the tectonic edifice and a transition from an Alpine- (13–18 °C km−1) to a Barrovian-type (28–36 °C km−1) geothermal gradient during the progress of the Alpine orogenic metamorphism in the Peloritani Mountains. The integration of these results allows the Peloritani Mountains to be considered as a constituent element of the Apennine orogenic domain formed during the progressive space–time transition from oceanic to continental subduction at the active convergent margin.