In Archean greenstone belts, magmatism is dominated by intrusive and volcanic rocks with tholeiitic affinities, as well as tonalite- and granodiorite-dominated large-volume batholiths, i.e., tonalite–trondhjemite–granodiorite (TTG) suites. These intrusions are associated with poorly documented mineralization (Cu-Au porphyries) that, in the Neoarchean Abitibi Subprovince (>2.79 to ~2.65 Ga), Superior Province, Canada, are associated with diorite bearing plutons, i.e., tonalite–trondhjemite–diorite (TTD) suites. The importance of TTG versus TTD suites in the evolution of greenstone belts and of their magmatic-hydrothermal systems and related mineralization is unconstrained. The aim of this study was to portray the chemistry and distribution of these suites in the Abitibi Subprovince. The study used data compiled by the geological surveys of Québec and Ontario to evaluate the chemistry of TTG and TTD suites and uncovered two coeval magmas that significantly differentiated (fractional crystallization mostly): 1) a heavy rare earth elements (HREE)-depleted tonalitic magma from high pressure melting of an hydrated basalt source; and 2) a hybrid HREE-undepleted magma that may be a mixture of mantle-derived (tholeiite) and tonalitic melts. The HREE-depleted rocks (mostly tonalite and granodiorite) display chemical characteristics of TTG suites (HREE, Ti, Nb, Ta, Y, and Sr depletion, lack of mafic unit, Na-rich), while the other rocks (tonalite and diorite) formed TTD suites. Tonalite-dominated magmatism, in the Abitibi Subprovince, comprises crustal melts as well as a significant proportion of mantle-derived magmas and this may be essential for Cu-Au magmatic-hydrothermal mineralizing systems.

This contribution explores the petrogenetic relationships between silicate and carbonatitic rocks in the Crevier Alkaline Intrusion (CAI, Québec, Canada). The CAI is located in the Proterozoic Grenville Province and is composed of a suite of undersaturated peralkaline rocks from ijolite to nepheline syenite and carbonatites. Petrogenetic relationships between different undersaturated alkaline igneous rocks, carbonate-bearing and carbonate-free nepheline syenite and carbonatites observed in the CAI suggest that (i) carbonate-bearing and carbonate-free silicate rocks are comagmatic with carbonatite, and that (ii) both silicate and carbonatitic liquids are fractionated from an ijolitic parental magma that has undergone liquid immiscibility. One of the observed facies is characterized by spectacular ocelli of carbonate-bearing nepheline syenite in a matrix of carbonatite. The younger nepheline syenite facies can be divided into two groups based on the presence or absence of magmatic carbonates. Both groups are characterized by the presence of pyrochlore-group minerals that carry the Nb-Ta mineralization. We specifically use accessory minerals such as zircon, pyrochlore and apatite to constrain the temporal and physicochemical parameters of the immiscibility process. By coupling (i) mineral textures, (ii) trace elements, (iii) Ti-in-zircon thermometry, and (iv) oxygen isotope compositions, we have traced the crystallization of zircon before, during and after the immiscibility process. The results allowed us to constrain the minimum temperature of this process at ∼815-865 °C. In addition, two magmatic populations of pyrochlore are identified through their petrographic and geochemical characteristics within the younger nepheline syenite facies. Pyrochlore from the earlier ocelli facies of carbonate-bearing nepheline syenite follow a Nb-Ta differentiation trend, whereas pyrochlore from the younger carbonate-free nepheline syenite follow a more classical Nb-Ti trend. Following the complete immiscibility between the silicate and carbonatitic liquids, the fractionation between Nb and Ta stopped while a new generation of Nb-rich pyrochlore grew, displaying a more classical Nb-Ti fractionation trend and a more constant Nb/Ta ratio in the nepheline syenite.

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