Formation of Topaz-Greisen by a Boiling Fluid: A Case Study from the Sn-W-Li Deposit, Zinnwald/Cínovec

Abstract

Abstract Zinnwald/Cínovec is one of the largest Li-Sn-W greisen deposits in Europe. Greisens in general are important hosts for many major ore deposits of several high-tech elements—most prominently Sn, W, and Li. However, the mechanisms of greisenization in relationship to ore formation are still not well understood, especially for the important case of fluoride-rich greisen. Here, we investigate the sequence and formation mechanism of the topaz-greisen in the Zinnwald/Cínovec deposit. Based on the mineral abundances, the alteration profile can be divided into four distinct zones: (1) rhyolite, (2) albitite, (3) low-degree greisen, and (4) high-degree greisen. In the greisen zones, almost all the feldspar has been replaced by topaz (up to 12 vol %) + quartz (up to 78 vol %), and the abundance of mica gradually decreases from 11 to 3 vol % with increasing degree of greisenization. Mass balance calculations indicate a net influx of F and silica during greisenization. Our observations are best explained by a two-stage greisenization process involving phase separation by boiling in the pore space of the sample: first an acidic HF-rich phase, likely a vapor, reacted with feldspar to form topaz and quartz in a dissolution-precipitation reaction. This reaction created substantial transient porosity, which was subsequently sealed by the precipitation of quartz and fluorite from a boiling liquid. We interpret the vapor and liquid as emerging from a common supercritical aqueous parental fluid. The characteristic sequence of creation of pore space by a vapor and the subsequent reduction of porosity by precipitation from the associated boiling liquid constrain the conditions and time available for ore formation. This study evaluates the mechanism of topaz greisenization and the controls on porosity evolution, which are crucial to ore element redistribution.