New P-T-X conditions for the formation of gem tsavorite garnet in the Voi area (southwestern Kenya)

International audienceTsavorite nodules-bearing deposits from southwestern Kenya are located in the Kurase Group, a metasedimentary unit of the Neoproterozoic Metamorphic Mozambique Belt. This unit is composed of graphitic paragneisses intercalated with metacarbonates and metaevaporites, surrounded by migmatites. The rocks underwent high grade metamorphism at 615-600 Ma. The main goal of this work is to link tsavorite formation to the metamorphic evolution of the Kurase Group. The new thermobarometric data indicate widespread granulite facies conditions at 800 +/- 50 degrees C and 10 +/- 1 kbar, with no significant difference between the tsavorite-bearing metasediments and the surrounding migmatitic gneisses. Pseudosection calculation for a tsavorite-bearing metasediment indicates that tsavorite grew close to peak-T conditions at around 800 degrees C. The tsavoritebearing formations have not melted extensively despite the high-grade metamorphism, in contrast with the surrounding migmatites. The lack of partial melting is probably due to an enrichment in vanadium, chromium and titanium in the protoliths that have increased the stability field of micas toward high-T. We suggest that the primary source of V and Cr was the evaporite-bearing mudstones. Crystallisation of high grade V and Cr rich tsavorite occurred in a closed system with little or no strain, in the presence of molten salts and H2S-S-8 fluids

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 typology and origin of tsavorite

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Age and Origin of the Tsavorite and Tanzanite Mineralizing Fluids in the Neoproterozoic Mozambique Metamorphic Belt

The genetic model previously proposed for tsavorite- (and tanzanite-) bearing mineralization hosted in the Neoproterozoic Metamorphic Mozambique Belt (stretching from Kenya through Tanzania to Madagascar) is refined on the basis of new Sm-Nd age determinations and detailed Sr-O-S isotope and fluid-inclusion studies. The deposits are hosted within meta-sedimentary series composed of quartzites, graphitic gneisses, calc-silicate rocks intercalated with meta-evaporites, and marbles. Tsavorite occurs either in nodules (also called "boudins") oriented parallel to the metamorphic foliation in all of the deposits in the metamorphic belt or in quartz veins and lenses located at the hinges of anticlinal folds (Lelatema fold belt and Ruangwa deposits, Tanzania). Gem tanzanite occurs in pockets and lenses in the Lelatema fold belt of northern Tanzania. The Sm-Nd isotopic data for tsavorites and tanzanites hosted in quartz veins and lenses from Merelani demonstrate that they formed at 600 Ma, during the retrograde metamorphic episode associated with the East African Orogeny. The tsavorites hosted in nodules do not provide reliable ages: their sedimentary protoliths had heterogeneous compositions and their Sm-Nd system was not completely rehomogenized, even at the local scale, by the fluid-absent metamorphic recrystallization. The initial 87Sr/86Sr isotopic ratios of calcite from marble and tanzanites from Merelani fit with the strontium isotopic composition of Neoproterozoic marine carbonates. Seawater sediment deposition in the Mozambique Ocean took place around 720 Ma. The quartz-zoisite O-isotopic thermometer indicates a temperature of formation for zoisite between 385 and 448 °C. The sulfur isotopic composition of pyrite (between 7.8 and 1.3\textperthousand V-CDT) associated with tsavorite in the Lelatema fold belt deposits suggests the contribution of reduced marine sulfate. The sulfur in pyrite in the marbles was likely derived from bacterial sulfate reduction which produced H2S. Fluid inclusion data from tsavorite and tanzanite samples from the Merelani mine indicate the presence of a dominant H2S-S8\textpm(CH4)\textpm(N2)\textpm(H2O)-bearing fluid. In the deposits in Kenya and Madagascar, the replacement of sulfate by tsavorite in the nodules and the boron isotopic composition of tourmaline associated with tsavorite are strong arguments in favor of the participation of evaporites in garnet formation

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