Scapolite occurrences are widely observed in the metasedimentary rocks exposed around the Khetri Copper Belt and adjoining Nim ka Thana copper mineralized area in western India. Amoeboidal to well-developed and rounded/elliptical-shaped marialitic scapolite (Na-rich end-member) rich zones with variable Cl contents ranging from 1.0 wt % to 2.9 wt % have been identified in proximity to the ore-bearing hydrothermal fluid activity zones. Although scapolite is formed as a product of regional metamorphism in many places, in this study, we propose a strong possibility that scapolite was formed by hydrothermal ore-bearing fluid interaction with metasediments. The evidence of hydrothermal activity and Cl sourcing is attributed to (i) the absence of evaporite beds in the area and no Na-rich plagioclase as inclusions within the scapolite suggesting the formation of marialitic scapolite from sodic plagioclase in the metasediments with the interacting hydrothermal fluid; (ii) an epithermal to mesothermal hydrothermal fluid with moderate salinity responsible for the Cu mineralization that is ascribed to be the source of Cl for the formation of marialitic scapolite; (iii) diffusion of SO2 in the scapolite in close association with the sulfide mineral phase (chalcopyrite) supporting the involvement of ore-bearing fluid in the development of scapolite; (iv) the absence of zoned scapolite, the spatial distribution of scapolite in a particular lithology, the occasional incorporation of sulfur into marialitic scapolite and the texture/geometry in the scapolite suggesting a broad hydrothermal linkage instead of a pure metamorphic origin.

Marble in the supracrustal rocks of the Lewisian Complex, Tiree, includes chlorine-bearing amphiboles, chlorine-rich apatite, sulphur-rich scapolite, albite and phlogopite, all of which are regarded as evidence for evaporites in other metamorphosed sequences. Titanite yields U–Pb ages of ∼1.6 Ga, i.e. late Laxfordian, which excludes a younger imprint of sodium metasomatism. Traces of anhydrite, and isotopically heavy pyrite, also indicate deposition from seawater. Elsewhere in the Hebrides, tourmaline in Lewisian Complex marbles may represent seafloor exhalative deposits. Combined, the evidence suggests Lewisian Complex supracrustal marbles formed in an evaporative environment, like other Palaeoproterozoic successions across the North Atlantic region.

Hyalotekite, a framework silicate of composition (Ba,Pb,K)4(Ca,Y)2Si8(B,Be)2 (Si,B)28F, is found in relatively high-temperature (⩾ 500°C) Mn skarns at Långban, Sweden, and peralkaline pegmatites at Dara-i-Pioz, Tajikistan. A new paragenesis at Dara-i-Pioz is pegmatite consisting of the Ba borosilicates leucosphenite and tienshanite, as well as caesium kupletskite, aegirine, pyrochlore, microcline and quartz. Hyalotekite has been partially replaced by barylite and danburite. This hyalotekite contains 1.29–1.78 wt.% Y2O3, equivalent to 0.172–0.238 Y pfu or 8–11% Y on the Ca site; its Pb/(Pb+Ba) ratio ranges 0.36–0.44. Electron microprobe F contents of Långban and Dara-i-Pioz hyalotekite range 1.04–1.45 wt.%, consistent with full occupancy of the F site. A new refinement of the structure factor data used in the original structural determination of a Långban hyalotekite resulted in a structural formula, (Pbl.96Bal.86K0.18)Ca2(B1.76Be0.24)(Sil.56B0.44)Si8O28F, consistent with chemical data and all cations with positive-definite thermal parameters, although with a slight excess of positive charge (+57.14 as opposed to the ideal +57.00). An unusual feature of the hyalotekite framework is that 4 of 28 oxygens are non-bridging; by merging these 4 oxygens into two, the framework topology of scapolite is obtained. The triclinic symmetry of hyalotekite observed at room temperature is obtained from a hypothetical tetragonal parent structure via a sequence of displacive phase transitions. Some of these transitions are associated with cation ordering, either Pb–Ba ordering in the large cation sites, or B–Be and Si–B ordering on tetrahedral sites. Others are largely displacive but affect the coordination of the large cations (Pb, Ba, K, Ca). High-resolution electron microscopy suggests that the undulatory extinction characteristic of hyalotekite is due to a fine mosaic microstructure. This suggests that at least one of these transitions occurs in nature during cooling, and that it is first order with a large volume change. A diffuse superstructure observed by electron diffraction implies the existence of a further stage of short-range cation ordering which probably involves both (Pb,K)–Ba and (BeSi,BB)–BSi.

Xenoliths in an olivine nephelinite from the McBride Province, North Queensland, include Cr-diopside lherzolites, spinel and garnet websterites, felsic, 2-pyroxene and garnet granulites, and hornblendites. The spinel and garnet websterites are interpreted as crystal segregations from olivine basalt or alkali olivine basalt magma at ∼ 12 kbar followed by isobaric cooling (to approximately 900–1000°C) and subsolidus reequilibration. Garnet and 2-pyroxene granulites are mineralogically and texturally distinct and are considered to represent relatively large degrees of crystallization of basaltic magmas at comparable or slightly lower pressures (8–12 kbar). Mafic and ultramafic xenoliths have been modified to varying degrees following the relatively recent influx of a H2O- and CO2-bearing fluid. Variable amounts of amphibole and mica developed in response to the introduced fluid and it is argued that some hornblendites are the end-products of this process acting on spinel websterites. Felsic and 2-pyroxene granulite xenoliths display only minor evidence of increased PH2O. Mineralogical and textural evidence indicates high-sulphur Ca-rich scapolite in several garnet granulites did not form in response to the increased fluid activities. It is proposed the scapolite was a primary cumulate phase precipitated from alkali basaltic magma under elevated fo2 and fso2 conditions.

Pegmatite cutting chlorite schist in the Minas fault at McKay Head, Nova Scotia, consists of Cl-rich (2.7–3.8 wt.% Cl) marialitic scapolite (EqAn21–32) with interstitial, apparently primary analcite, hematite and rutile, and later (including vug-lining) analcite, pyrite, chlorite, titanite and calcite, and cross-cutting epidote veins. Some of the latter phases might have crystallized from residual pegmatitic fluids. Unlike many other primary scapolite-bearing igneous rocks, the McKay Head occurrence has compositional affinities with mafic (rather than felsic) systems: it is enriched in transition metals (e.g. Cr≤53 ppm), and has very low LILE concentrations (e.g. Rb<10 ppm; U<1 ppm; Th<2 ppm; Ba<20 ppm) and Rb/Sr ratios (~0.05). The presence of interstitial rutile and hematite rather than ilmenite indicates that the pegmatitic fluid was oxygenated late (T~400°C) in its crystallization history.

The pegmatite is interpreted to be related to highly sodic hydrothermal solutions derived from (or affected by) early Carboniferous evaporites of the Windsor or Horton groups. Compositionally-similar fluids, perhaps also related to an evaporite source, may be responsible for a regional, early Carboniferous Na-metasomatic event that altered a suite of alkaline granitoid intrusions shortly after their emplacement.

Silvialite, ideally Ca4Al6Si6O24SO4, is tetragonal, I4/m, Z = 2, with a = 12.160(3), c = 7.560(1) Å, V = 1117.9(8) Å3, c:a = 0.6217:1, ω = 1.583, ε = 1.558 (uniaxial negative), Dm = 2.75 g/cm3, Dcalc = 2.769 g/cm3 and H (Mohs) = 5.5. It is transparent and slightly yellow, has a good {100} cleavage, chonchoidal fracture, white streak and a vitreous lustre. It occurs in upper-mantle garnet-granulite xenoliths hosted by olivine nephelinite, from McBride Province, North Queensland, Australia. The empirical formula, derived from electron-microprobe analysis, is (Na1.06Ca2.86)(Al4.87Si7.13)O24 [(SO4)0.57(CO3)0.41]. Crystal-structure refinement shows disordered carbonate and sulfate groups along the fourfold axis. Silvialite is a primary cumulate phase precipitated from alkali basalt at 900–1000°C and 8–12 kbar under high fSO2 and fO2. The name silvialite, currently used in literature to describe the sulfate analogue of meionite, was suggested by Brauns (1914).

Twenty-seven scapolite samples from various localities and with compositions between Me 6–93 were obtained using electron microprobe analysis (EMPA). Their unit-cell parameters were obtained using synchrotron high-resolution powder X-ray diffraction (HRPXRD) data and Rietveld structure refinements using space group P42/n. The EMPA data show the well-known discontinuity at Me 75. In addition, the unit-cell parameters, especially c, show a discontinuity at Me 75 (=five Al atoms per formula unit, apfu), ideally NaCa3[Al5Si7O24](CO3), where the scapolite solid solution is divided into two (Me% = [Ca/(Ca + Na + K)] × 100). A maximum c parameter value occurs at Me 37.5 (=four Al apfu ideally), where complete Al–Si, Na–Ca, and Cl–CO3 order occurs. The unit-cell volume, V, varies smoothly with Me% and Al apfu across the series.