Calcioancylite-(La), ideally (La,Ca)2(CO3)2(OH,H2O)2, has been discovered from nepheline syenite of the Gejiu alkaline complex in the Honghe Hani and Yi Autonomous Prefecture, Yunnan Province, China. The mineral occurs as aggregates of subhedral grains, and the size of single crystals varies between 5–20 μm. Calcioancylite-(La) is colourless to pale pinkish grey and has transparent to translucent lustre. It is brittle with a Mohs hardness of 4. The calculated density is 4.324 g/cm3. The mineral is biaxial (−), with α =1.662, β = 1.730, γ = 1.771, 2Vmeas. = 70°(1) and 2Vcalc. = 73°. Electron microprobe analysis for holotype material yielded an empirical formula of (La0.58Ce0.55Pr0.14Nd0.10Ca0.39Sr0.20K0.04)Σ2.00(CO3)2[(OH)1.25F0.06⋅0.69H2O]Σ2.00. Calcioancylite-(La) is orthorhombic, with space group Pmcn, a = 5.0253(3) Å, b = 8.5152(6) Å, c = 7.2717(6) Å, V = 311.17(4) Å3 and Z = 2. By using single-crystal X-ray diffraction, the crystal structure has been determined and refined to a final R1 = 0.0652 on the basis of 347 independent reflections (I > 2σ). The seven strongest powder X-ray diffraction lines [d in Å (I) (hkl)] are: 2.334 (100) (013), 2.970 (80) (121), 4.334 (75) (110), 3.678 (68) (111), 2.517 (55) (200), 2.647 (47) (031) and 2.077 (44) (221). Calcioancylite-(La) is the La-analogue of calcioancylite-(Ce) and is a new member of ancylite-group minerals. The mineral and its name have been approved by the Commission on New Minerals, Nomenclature and Classification of the International Mineralogical Association (IMA2021-090).

The Cnoc Rhaonastil minor dolerite intrusion on Islay, NW Scotland represents a single body of alkali olivine basalt magma which differentiated in situ, from leucodolerite, through teschenite to minor nepheline syenite. The syenites occur as isolated nests and pegmatitic schlieren within the leucodolerite, and schlieren of gabbroic pegmatite also occur at the margin of the teschenite. The differentiated rocks contain pyroxene, amphibole and biotite of variable compositions which reflect both primary fractionation processes and late-stage deuteric alteration and reaction.Mafic phases within the gabbroic pegmatite, teschenite and syenite are typically rimmed and speckled with biotite, the composition of which is controlled by the local environment of crystallization. The nepheline syenites contain primary ferro-kaersutite which, where in contact with interstitial patches, has been altered to arfvedsonite, which occasionally contains up to 1.2 wt.% ZrO2. The occurrence of Zr-arfvedsonite (and of Zr-aegirine) in interstitial patches suggests that variably trace element-enriched domains existed within the residual melts on very small scales.

North Motzfeldt is an intrusive igneous centre within the Igaliku (formerly spelt Igaliko) complex, Gardar Province, South Greenland. A detailed field description of the centre is given, with preliminary geochemical and isotopic data. The North Motzfeldt centre is intruded into Ketilidian granitoid basement rocks, and current exposure retains parts of the original roof against earlier Gardar eruptives and clastic sediments of the Eriksfjord formation. The unconformity between the Ketilidian and the overlying Eriksfjord is believed to have been crucial in the siting of the centre. The centre is subdivided into two major units, NM1 and NM2. This was followed by significant peralkaline nepheline microsyenite in sheets, characterized by rare element-rich accessory minerals including rinkite-mł sandrite, pyrochlore and låvenite. A significant microsyenite body is called NM3. A preliminary Rb-Sr isochron of 1226±27 Ma indicates a far younger age for the centre than previously thought (~;1350 Ma). Cross-cutting relationships between North Motzfeldt and rocks of the adjacent Motzfeldt centre require a reappraisal of the chronology of Motzfeldt magmatism. We suggest that rocks previously believed to comprise the Motzfeldt centre represent the products of multiple phases of magmatism from Early- to Mid-Gardar times.

The Grønnedal-Íka ring complex (1299 ± 17 Ma) in the Gardar province, South Greenland is composed of a range of layered nepheline syenites which were intruded at a late stage by xenolithic syenite and a plug of carbonatite. The complex was subsequently intruded by a variety of basic dykes, including olivine dolerites, kersantites, vogesites, spessartites, camptonites and an alnöite, and then extensively faulted. The nepheline syenite magmas, produced by fractional crystallisation of basic magmas, show a range in δ13C (−3.86 to −7.57‰) and δ18O (8.27 to 15.12‰), distinctly different to the carbonatites which form a tight group with average δ13C = −4.31 + 0.22 ‰, (1 s.d.) and average δ18O = 7.18 ± 0.41‰ (1 s.d.). Initial 87Sr/86Sr isotope ratios (typically 0.703) suggest the syenites and carbonatites have not assimilated crustal rocks, and therefore the C and O isotope variation within each group is a result of isotopic evolution during fractional crystallisation. A suite of lamprophyre dykes (δ13C −3.86 to −7.86‰ and δ18O 9.12 to 10.81‰) form a coherent group whose stable isotope compositions overlap part of the syenite field, and again are distinctly different from the carbonatites. A single alnöite has δ13C = −3.32‰ and δ18O = 12.34‰ C and O isotope ratios are consistent with origins of syenitic and lamprophyric magmas from a similar source. Despite geochemical evidence which suggests a genetic link between nepheline syenites and carbonatites, C and O isotopic evidence shows that they are not related directly by liquid immiscibility. Comparisons are made between similar rock types from Grønnedal-Íka and from the Gardar Igaliko Dyke Swarm. The possible role of F in controlling δ13C and δ18O during crystallisation of calcite from carbonatite magmas is discussed.

It is now generally agreed that the term ‘agpaitic’ should be restricted to peralkaline nepheline syenites (and phonolites) containing minerals such as eudialyte and rinkite, that is complex silicates of Zr, Ti, the rare earth elements (REE), and F and other volatiles. There are, however, cases of transition into more common types of nepheline syenites containing zircon, titanite, ilmenite, etc.

The agpaitic rocks are characterized by extremely high contents of rare elements such as Li, Be, Nb, Ta, REE, Zr, Th, etc. and of volatiles, first of all F and Cl. This gives rise to a wealth of mineral species, more than 500 in the Lovozero and Khibina complexes of the Kola peninsula, about 250 in Mont Saint-Hilaire, Quebec, Canada, and about 200 in the type locality, the Ilímaussaq complex, South Greenland.

These rocks have very long melting intervals and solidus temperatures as low as 500 to 400°C. They are accompanied by a gas phase rich in methane and other hydrocarbons and most probably also by sodium-rich fluids as indicated by the presence of minerals such as ussingite (NaAlSi3O8·NaOH) and villiaumite (NaF) and of pegmatites and hydrothermal veins rich in sodium and rare and volatile elements.

Agpaitic nepheline syenites are considered to have been formed by consolidation of melts oversaturated in alkalis, especially sodium, under conditions preventing the volatiles from escaping. These melts have been derived by extreme fractionation processes in alkali basaltic or nephelinitic magmas. The main stage of crystallization of the melts is characterized by minerals such as nepheline (sometimes also sodalite), alkali feldspars, arfvedsonite, aegirine and eudialyte, but the most highly developed, hyperagpaitic lujavrites of the Ilímaussaq complex have been formed from melts with extreme concentrations of sodium and volatiles resulting in the formation of naujakasite instead of nepheline, ussingite instead of sodalite and alkali feldspars, and steenstrupine instead of eudialyte. During the late stages of crystallization, sodium-rich fluids are the cause of late- and postmagmatic alteration and of the formation of hydrothermal mineralizations. The late stages are characterized by water-soluble sodium-rich minerals of which more than 80 have been found in the Khibina and Lovozero complexes.

The mineralogy, including the accessory phases låvenite, rosenbuschite, and catapleiite, and consequent petrogenetic implications have been investigated for a group of four overlapping nepheline syenite complexes (Chikala, Chaone, Mongolowe, and Chinduzi) and for spatially associated silica-saturated and over-saturated perthosites, from the northern part of the Chilwa Alkaline Province, Malawi.

The complexes are thought to have formed by injection into high-level chambers of magma pulses genetically related to a common source magma at depth. Evidence for the source magma is preserved in salitic cores observed in the pyroxenes and a trend to more hedenbergite-rich compositions is believed to have formed by evolution of this magma. Subsequent trends of acmite enrichment followed magma injection into the higher-level chambers; the actual pyroxene trend associated with each individual complex is a function of the evolution attained by the source magma, oxidation potential, and perhaps even alkali activity. On the basis of such a two-stage model, the pyroxene data suggest emplacement of the Chaone and Mongolowe magmas somewhat earlier than that of Chikala, with the Chinduzi magma migrating even later.

Amphiboles and biotites are believed to have formed after high-level injection of the magmas. Their compositions broadly reflect the nature of the crystallizing pyroxenes in that magnesian hastingsitic hornblendes and more Mg-rich biotites are associated with more Mg-rich sodic pyroxenes, whereas katophorites and annite-rich micas are generally associated with sodic pyroxenes somewhat richer in hedenbergite. Sub-solidus crystallization in some of the complexes is represented by aegirine and magnesio-arfvedsonite. Nepheline compositions indicate broadly similar crystallization temperatures within the complexes, namely 950 to 750°C. Oxygen fugacities for these magmas obtained from biotite/annite compositions vary from 10−19 to 10−14 bars for this temperature range. Mineralogical data, particularly from pyroxenes and amphiboles, strongly suggest that the perthosites, spatially associated with the nepheline syenite complexes, are genetically unrelated.

Naujakasite (Na6(Fe,Mn)Al4Si8O26) is a characteristic, rock-forming mineral of hyperagpaitic naujakasite lujavrite (arfvedsonite + naujakasite + steenstrupine + albite ± relict nepheline ± microcline ± ussingite) from the Ilímaussaq complex, South Greenland, and is only known from this complex. The qualitative stability relationships of naujakasite-bearing, low-variance liquidus mineral assemblages at near-solidus conditions in lujavritic magma can be modelled within the six-component system Si-Al-Fe-Na-O-H. The modelling suggests that an uncommon combination of elevated water activity and low oxygen fugacity is needed to stabilize arfvedsonite + naujakasite mineral assemblages in highly sodic liquids. These conditions are incompatible with the stable coexistence of aegirine and arfvedsonite. They are met in the arfvedsonite-bearing lujavrites of Ilímaussaq, but apparently not in rocks of similar composition in the Khibina and Lovozero complexes, Kola Peninsula, where aegirine- or aegirine-arfvedsonite-bearing mineral assemblages are characteristic. Liquid lines of descent leading to crystallization of naujakasite have to pass through the albite+nepheline+arfvedsonite liquidus field in the Si-Al-Fe-Na-O-H system, reaching this field at the high-Na side of the albite-nepheline-arfvedsonite plane.

Nearly 70 new Nd isotope analyses are presented for plutonic orthogneisses from the Grenvillian Central Metasedimentary Belt (CMB) in order to test a back-arc aulacogen model for its origin. Nd isotope signatures of metaplutonic rocks are used as probes of the formation age of the crust at depth, revealing sharp boundaries between old crustal blocks and juvenile (1.2–1.35 Ga) Elzevirian-age crust. Firstly, a hidden block of old crustal basement is revealed between areas of juvenile crust south of Douglas, Ontario. Secondly, TDM ages refine the boundary between juvenile crust and old basement (1.35–1.55 Ga) within the Weslemkoon batholith, showing this pluton to be a polygenetic stitching pluton that straddles a hidden crustal boundary. Finally, the CMB boundary zone is shown to form a sharp age boundary between juvenile and old crustal domains, and is interpreted as a reactivated rift-bounding normal fault. When the distribution of rift-related alkaline rocks is compared with these crustal boundaries, the Bancroft nepheline syenite suite is centrally located in a juvenile ensimatic zone between blocks of old basement. Such a location, near the axis of a juvenile crustal segment, implies emplacement late in the rifting process. Similarly, the Blue Mountain nepheline syenite appears to post-date an earlier rifting event to the southeast. Hence, a multi-stage model is proposed for the evolution of a back-arc aulacogen, which is consistent with the distribution of marble and volcanic/plutonic units in the CMB. The model places the Bancroft nepheline syenites in a precise plate tectonic context for the first time.