ALBERT

Description: In this study, we report the occurrence of zircon coronae textures in metapelitic granulites of the Ivrea–Verbano Zone. Unusual zircon textures are spatially associated with Fe–Ti oxides and occur as (1) vermicular-shaped aggregates 50–200 µm long and 5–20 µm thick and as (2) zircon coronae and fine-grained chains, hundreds of micrometers long and ≤ 1 µm thick, spatially associated with the larger zircon grains. Formation of such textures is a result of zircon precipitation during cooling after peak metamorphic conditions, which involved: (1) decomposition of Zr-rich ilmenite to Zr-bearing rutile, and formation of the vermicular-shaped zircon during retrograde metamorphism and hydration; and (2) recrystallization of Zr-bearing rutile to Zr-depleted rutile intergrown with quartz, and precipitation of the submicron-thick zircon coronae during further exhumation and cooling. We also observed hat-shaped grains that are composed of preexisting zircon overgrown by zircon coronae during stage (2). Formation of vermicular zircon (1) preceded ductile and brittle deformation of the host rock, as vermicular zircon is found both plastically and cataclastically deformed. Formation of thin zircon coronae (2) was coeval with, or immediately after, brittle deformation as coronae are found to fill fractures in the host rock. The latter is evidence of local, fluid-aided mobility of Zr. This study demonstrates that metamorphic zircon can nucleate and grow as a result of hydration reactions and mineral breakdown during cooling after granulite-facies metamorphism. Zircon coronae textures indicate metamorphic reactions in the host rock and establish the direction of the reaction front.

Description: Quartz has been replaced by magnesium silicate hydrate cement at the Feragen ultramafic body in south-east Norway. This occurs in deformed and recrystallized quartz grains deposited as glacial till covering part of the ultramafic body. Where the ultramafic body is exposed, weathering leads to high-pH (∼ 10), Mg-rich fluids. The dissolution rate of the quartz is about 3 orders of magnitude higher than experimentally derived rate equations suggest under the prevailing conditions. Quartz dissolution and cement precipitation start at intergranular grain boundaries that act as fluid pathways through the recrystallized quartz. Etch pits are also extensively present at the quartz surfaces as a result of preferential dissolution at dislocation sites. Transmission electron microscopy revealed an amorphous silica layer with a thickness of 100–200 nm around weathered quartz grains. We suggest that the amorphous silica is a product of interface-coupled dissolution–precipitation and that the amorphous silica subsequently reacts with the Mg-rich, high-pH bulk fluid to precipitate magnesium silicate hydrate cement, allowing for further quartz dissolution and locally a complete replacement of quartz by cement. The cement is the natural equivalent of magnesium silicate hydrate cement (M-S-H), which is currently of interest for nuclear waste encapsulation and for environmentally friendly building cement, but it has not yet been developed for commercial use. This study provides new insights that could potentially contribute to the further development of M-S-H cement.