The Ibero-Armorican arc is continuous between Iberia and Armorica; its curvature increased with time due to subduction followed by continental collision; indentation produced left lateral transpression in Iberia and right-lateral transpression in Armorica. It is argued that whereas the antithetic shear is predominant in Iberia, in Armorica a synthetic shear prevailed because the identer rotated anticlockwise between the opposed forelands of the Variscan Fold Belt. It is proposed that the major Rheic ocean, closed by subduction towards the inner part of the arc, solving the space problem of centripetal vergences.
High-grade metamorphic rocks associated with S-type granites are recorded in the Central Iberian Zone, Iberian Variscides. Though most of these occur as inferred metamorphic core complexes affiliated with detachment faults, others, such as the Figueira de Castelo Rodrigo–Lumbrales Anatectic Complex, crop out between low-grade metamorphic rocks separated by steeply-dipping strike-slip shear zones, such as the Juzbado–Penalva do Castelo Shear Zone. Our structural analysis has been able to constrain two major deformation stages during the Variscan D 3 : (a) D 3a ductile deformation event, with clear sinistral kinematic criteria; and (b) D 3b thrusting ductile–brittle deformation event. The petrological investigation confirmed the jump in metamorphic grade between the host rocks and the anatectic complex. P–T estimates on calc-silicate rocks interlayered with the metapelites of the anatectic complex provided minimum metamorphic peak conditions of T = 761 ± 50°C and P = 5.0 ± 1.0 kbar. However, petrological modelling results show that P–T conditions must have exceeded T > 800°C. Both structural and geothermobarometric data support a two-step model for the exhumation of the Anatectic Complex, including a 5 – 8 km vertical exhumation along a 65 – 100 km horizontal displacement due to a simple shear-dominated transpression mechanism during the Variscan D 3 events. Supplementary material: The petrology data, mineral chemistry analyses of the calc-silicate units and EPMA analytical conditions, and the P–T modelling methodology can be found at https://doi.org/10.6084/m9.figshare.c.3785648