Abstract

Aluminum phosphate–sulfate (APS) minerals occur as disseminated crystals in a wide range of geological environments near the Earth’s surface, including weathering, sedimentary, diagenetic, hydrothermal, metamorphic and also postmagmatic systems. Their general formula is AB3(XO4)2(OH)6, in which A, B and X represent three different crystallographic sites. These minerals are known to incorporate a great number of chemical elements in their lattice and to form complex solid-solution series controlled by the physicochemical conditions of their formation (Eh, pH, activities of constituent cations, P and T). These minerals are particularly widespread and spatially related to hydrothermal clay-mineral parageneses in the East Alligator River Uranium Field (EARUF) environment associated with uranium orebodies in the Proterozoic Kombolgie basin of the Northern Territories, Australia. This field contains several high-grade unconformity-related uranium deposits, including Jabiluka and Ranger. Both petrography and chemical data are used to discuss the significance of APS minerals in the alteration processes from the EARUF. The wide range of chemical compositions recorded in APS is essentially due to coupled substitutions of Sr for the LREE and of S for P at the A and X sites, respectively. The major variations of the APS solid-solution series mainly consist of the relative proportions of svanbergite, goyazite and florencite end-members. The APS minerals result from the interaction of oxidizing and relatively acidic fluids with aluminous host-rocks enriched in monazite. The spatial distribution of these minerals and their compositional variation around the uranium orebodies allow us to consider them as good tracers of redox and pH paleo-conditions responsible for the development of fronts during the alteration processes, and hence as potential tools for mineral exploration.

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