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The 3D microstructure and compositional zoning of garnet populations in micaschists from the Kolvik and Bekkarfjord nappes indicate the quasi‐equilibration of their major components across the rock matrices during interface‐controlled, size‐independent garnet growth. There is microstructural evidence for foliation‐parallel, small‐scale resorption of garnet rims in the Kolvik Nappe, influencing the metamorphic peak conditions obtained from thermodynamic modelling. The local chemical compositions of rims less affected by resorption indicate a peak temperature of ~630°C, which is ~40°C higher than the temperature obtained from resorbed rims of the largest garnet crystal. Using a diffusion geospeedometry approach that considers the geometry of the compositional zoning of the garnet population, as well as the higher, more realistic peak temperature, a duration of 1 to 4.9 Myr is obtained for garnet growth in the Kolvik Nappe. This is approximately 1 order of magnitude faster than duration estimates obtained when using the apparent, lower temperature estimated from the resorbed garnet rims. Concomitantly to garnet growth in the Kolvik Nappe, garnet overgrowths formed in the Bekkarfjord Nappe for circa 2.5 Myr at metamorphic peak temperatures of ~560°C. The garnet growth durations obtained here are comparable with the uncertainty on the Lu–Hf garnet–whole rock isochron ages of 419.9 ± 2.4 Ma and 423.0 ± 1.9 Ma, previously obtained for these rocks. These results provide new insight into the timescales of repeated Barrovian‐type metamorphic events experienced by the lower nappes of the Kalak Nappe Complex during the Caledonian Orogeny in Arctic Norway. This study emphasizes the importance of microstructural and chemical characterization of garnet populations in assessing metamorphic crystallization mechanisms and the extent of equilibration of garnet‐forming components during prograde metamorphism. Moreover, our results provide means for reducing the uncertainty on metamorphic durations obtained via diffusion geospeedometry and, so, contributing to our understanding of geological timescales and processes. [ABSTRACT FROM AUTHOR]

Manganese (Mn) dendrites are a common type of mineral dendrite that typically forms two-dimensional structures on rock surfaces. Three-dimensional (3-D) Mn dendrites in rocks have rarely been reported, and so their growth implications have largely escaped attention. Here, we combined high-resolution X-ray and electron-based data with numerical modeling to give the first detailed description of natural 3-D Mn dendrites (in clinoptilolite tuffs) and elucidate their growth dynamics. Our data show that 3-D dendrite growth occurred by accretion of Mn-oxide nanoparticles formed when Mn-bearing fluids mixed with oxygenated pore water. The geometry of the resulting structures is sensitive to ion concentrations, the volume of infiltrating fluid, and the number of fluid pulses; thus, 3-D dendrites record the hydrogeochemical rock history. [ABSTRACT FROM AUTHOR]