New typology and origin of tsavorite based on trace-element chemistry

New electron-microprobe analyses of 'tsavorites' from the Neoproterozoic Metamorphic Mozambique Belt deposits allow the characterization of green grossular according to its trace-element chemistry (V, Cr, Mn). Five chemical types are defined: type 1, vanadian grossular with V > Cr > Mn (in atoms per formula unit); type 2, vanadian grossular with V > Mn > Cr; type 3, Mn-bearing vanadian grossular with Mn > V > Cr; type 4, Mn-bearing chromian grossular with Mn > Cr > V; and type 5, Cr- and Mn-bearing grossular with Cr > Mn > V. These types are also characterized by different absorption spectra in the ultraviolet-visible-near infrared. Type 1 tsavorite spectra show a total absorption below 430 nm due to the high vanadium contents. Type 2 tsavorite spectra present the classical absorption bands of V. Types 3 and 4 tsavorite spectra display additional shoulders at 407 and 408 nm due to Mn2+, whereas spectra of Cr-bearing types 4 and 5 tsavorite show the two additional bands of Cr3+ at 697 and 701 nm. The different absorption spectra also indicate Fe2+-Ti4+ charge transfer. We measured OH equivalent to 0.08 to 0.38 wt% eq. H2O within the structure. Concentrations of vanadium, chromium and manganese are good chemical "fingerprints" for determining the geographic provenance of economic tsavorite from Kenya, Tanzania and Madagascar

New aspects and perspectives on tsavorite deposits

Tsavorite, the vanadian variety of green grossular, is a high value economic gemstone. It is hosted exclusively in the metasedimentary formations from the Neoproterozoic Metamorphic Mozambique Belt. The deposits are mined in Kenya, Tanzania and Madagascar and other occurrences are located in Pakistan and East Antarctica. They are located within metasomatized graphitic rocks such as graphitic gneiss and calc-silicates, intercalated with meta-evaporites. Tsavorite is found as primary deposits either in nodule (type I) or in quartz vein (type II), and in placers (type III). The primary mineralizations (types I and II) are controlled by lithostratigraphy and/or structure. For the African occurrences, the protoliths of the host-rocks were deposited at the beginning of the Neoproterozoicwithin a marine coastal sabkha environment, located at the margin of the Congo–Kalahari cratons in the Mozambique Ocean. During the East African–Antarctican Orogeny, the rocks underwent high amphibolite to granulite facies metamorphism and the formation of tsavorite deposits occurred between 650 and 550 Ma. The nodules of tsavorite were formed during prograde metamorphism, calcium coming from sulphates and carbonates, whereas alumina, silicates, vanadium and chromium probably came from clays and chlorite. The veins were formed during the deformation of the metasedimentary platform units which experienced shearing, leading to the formation of fault-filled veins. Metasomatism developed during retrograde metamorphism. The metasedimentary sequences are characterized by the presence of evaporitic minerals such as gypsum and anhydrite, and scapolite. Evaporites are essential as they provide calcium and permit the mobilization of all the chemical elements for tsavorite formation. The H2S–S8 metamorphic fluids characterized in primary fluid inclusions of tsavorites and the δ11B values of coeval dravite confirm the evaporitic origin of the fluids. The V2O3 and Cr2O3 contents of tsavorite range respectively from 0.05 to 7.5 wt.%, while their δ18O values are in the range of 9.5–21.1‰. The genetic model proposed for tsavorite is metamorphic, based on chemical reactions developed between an initial assemblage composed of gypsum and anhydrite, carbonates and organic matter deposited in a sabkha-like sedimentary basin