Contrary to the southern Appalachians, where Alleghanian magmatism is widespread and well documented, the expressions of magmatism in the Canadian Appalachians are limited. In this study, a suite of leucocratic dykes from the Cape Spencer area in southern New Brunswick, Canada, were investigated to determine the nature, timing and source of these magmas using zircon and monazite U-Pb geochronology, whole-rock geochemistry and Nd-Hf isotopes. An LA-ICP-MS U-Pb monazite Alleghanian age of 273.7 ± 1.3 Ma obtained for these dykes constitutes a new example of magmatism in the northern segment of the orogen, where significant strike-slip movement and reheating have been the primary markers of the Alleghanian Orogeny. These metaluminous leucocratic dykes are enriched in light rare elements, U and Th; depleted in high-field strength elements (HFSE; Nb, P, Ti); and have slight negative Europium anomalies [(Eu/Eu*)N = 0.72–0.95]. All the dykes samples have negative εNd(t) values (−9.76 to −5.7), negative εHf(t) values (−1.8 to −1.0) and Mesoproterozoic Nd depleted-model ages (TDM = 1371–1618 Ma). The geochemical and isotopic characteristics suggest that the dykes were formed by the partial melting of lower crust that assimilated Meguma metasedimentary rocks and/or Avalonian sedimentary rocks, following terminal subduction of the Rheic Ocean and thermal re-equilibration during the Alleghanian orogeny. The effects of the closure of the Rheic Ocean in the oblique collision between composite Laurentia and Gondwana were, to a certain extent, accommodated along the Minas Fault Zone, where magmatism and regional fluid flow were concentrated.

The Neoproterozoic Sevattur complex is composed essentially of calcite and dolomite carbonatites together with pyroxenites and diverse syenites. This work reports the compositions and paragenesis of different pyrochlore generations hosted by albitite veins in this complex. The pyrochlore are distinctive, being exceptionally rich in uranium (26 to 36 wt.% UO2). Five types of pyrochlore (Pcl-I to Pcl-V) are recognised on the basis of composition and texture. With the exception of Pcl-V, the majority of the pyrochlore (Pcl-II to Pcl-IV) are surrounded by a thick orbicular mantle of Ba-rich potassium feldspar. This mantle around Pcl-V is partially-broken. Pcl-I is restricted to the cores of crystals, and associated with Pcl-II and -III and is relatively rich in Nb (0.53–0.62 apfu) together with more A-site vacancies (0.37–0.71 apfu) compared to Pcl-II to Pcl-IV. Other pyrochlore (Pcl-II to Pcl-IV) are characterised by elevated Ca and Ti compared to Pcl-I, which are related to the (3Nb5+ + Na+ → 3Ti4+ + U4+) and (2Nb5+ → 2Ti4+ + Ca2+) substitutions, respectively. These substitutions represent replacement of Pcl-II to Pcl-IV. Alteration and Ba-enrichment in all the pyrochlore are marked by interaction with an externally-derived Ba-rich hydrothermal fluid following the (2Nb5+ → 2Ti4+ + Ba2+) substitution. This substitution, coupled with extensive metamictisation leads to the formation of Ba-rich (15.9–16.3 wt.% BaO) patchy-zoned Pcl-V. The orbicular mantles around Pcl-I to Pcl-IV have prevented extensive metamictisation and extensive secondary alteration compared to Pcl-V, where mantling is partially disrupted. The compositional and textural variation suggests that Pcl-II to Pcl-IV form by nucleation on Pcl-I, and are transported subsequently as antecrysts in the host albitite.