Bogusław Bagiński

Compositional variation in the chevkinite group: new data from igneous and metamorphic rocks

Abstract Electron microprobe analyses are presented of chevkinite-group minerals from Canada, USA, Guatemala, Norway, Scotland, Italy and India. The host rocks are metacarbonates, alkaline and subalkaline granitoids, quartz-bearing pegmatites, carbonatite and an inferred K-rich tuff. The analyses extend slightly the range of compositions in the chevkinite group, e.g. the most MgO-rich phases yet recorded, and we report two further examples where La is the dominant cation in the A site. Patchily-zoned crystals from Virginia and Guatemala contain both perrierite and chevkinite compositions. The new and published analyses are used to review compositional variation in minerals of the perrierite subgroup, which can form in a wide range of host rock compositions and over a substantial pressure-temperature range. The dominant substitutions in the various cation sites and a generalized substitution scheme are described.

REE partitioning between apatite and melt in a peralkaline volcanic suite, Kenya Rift Valley

Abstract Electron microprobe analyses are presented for fluorapatite phenocrysts from a benmoreite-peralkaline rhyolite volcanic suite from the Kenya Rift Valley. The rocks have previously been well characterized petrographically and their crystallization conditions are reasonably well known. The REE contents in the M site increase towards the rhyolites, with a maximum britholite component of ~35 mol.%. Chondrite-normalized REE patterns are rather flat between La and Sm and then decrease towards Yb. Sodium and Fe occupy up to 1% and 4%, respectively, of the M site. The major coupled substitution is REE3+ + Si4+ ↔ Ca2+ + P5+. The substitution REE3+ + Na+ ↔ 2Ca2+ has been of minor importance. The relatively large Fe contents were perhaps facilitated by the low fO₂ conditions of crystallization. Zoning is ubiquitous and resulted from both fractional crystallization and magma mixing. Apatites in some rhyolites are relatively Y-depleted, perhaps reflecting crystallization from melts which had precipitated zircon. Mineral/glass (melt) ratios for two rhyolites are unusually high, with maxima at Sm (762, 1123).

Apatite-supergroup minerals in UK Palaeogene granites: composition and relationship to host-rock composition

The Palaeogene granites of Scotland and Northern Ireland range mineralogically from biotite ± amphibole – through fayalite-hedenbergite– to riebeckite-bearing types and compositionally from metaluminous to peralkaline. Five members of the apatite supergroup of minerals are reported from the granites. Apatite is a relatively early-crystallizing phase in all rocks, whilst britholite crystallized during later magmatic stages in about half the samples, independent of granite type. There is a major composition gap between apatite and britholite, ranging from ~10 to 48 % of the britholite component. The dominant substitution mechanism was REE 3+ +Si 4+ = Ca 2+ +P 5+ , although the substitution Na + +REE 3+ = 2Ca 2+ occurred in the more peralkaline granites. Zonation is common in apatite and britholite and is ascribed to kinetic effects.

Chevkinite-group minerals from Russia and Mongolia: new compositional data from metasomatites and ore deposits

Abstract Electron-microprobe analyses of Russian and Mongolian chevkinite-group minerals from little-known host lithologies, including various metasomatic rocks, quartzolites and an apatite deposit, are presented. The mineral species analysed include chevkinite-(Ce), perrierite-(Ce), polyakovite-(Ce) and Sr- and Zr-rich perrierite-(Ce). Compositional variation in the Sr-rich members of the group is broadly represented by the exchange vector (Fe + Mn + Al + REE) ↔ (Ca + Sr + Ti + Zr). Despite the varied parageneses, the chevkinite-(Ce) compositions are similar to previously published data. Many crystals have strong internal compositional variations, partly produced during primary crystallization and partly during low-temperature hydrothermal alteration.

The central Kenya peralkaline province: a unique assemblage of magmatic systems

Abstract The review focuses on the evolution of five contiguous peralkaline salic complexes in the south-central Kenya Rift Valley, stressing new developments of general significance to peralkaline magmatism. The complexes have evolved dominantly by combinations of fractional crystallization and magma mixing; volatile-melt interactions, remobilization of plutonic rocks and crystal mushes, and carbonate-silicate liquid immiscibility have been additional petrogenetic processes. Geochemical and experimental studies have shown that pantelleritic magmas can be generated by fractional crystallization of trachyte and high-silica rhyolite. Melts of comenditic composition were also formed by fractionation of trachyte but also locally by partial melting of syenites. Studies of apparent partition coefficients have provided some of the first data on element distribution between phenocrysts and peralkaline silicic melts. Compositional zonation has been ubiquitous in the complexes, probably a result of the very low viscosity of the magmas.

The Palaeogene Eskdalemuir dyke, Scotland: long-distance lateral transport of rhyolitic magma in a mixed-magma intrusion

Abstract The Palaeogene Eskdalemuir dyke, part of the Mull dyke swarm in the Southern Uplands of Scotland, is ~60 km long and up to 40 m thick. Its southern tip is 230 km from the inferred source on Mull. The dyke is composite, with tholeiitic basaltic margins and a vitreous central facies ranging from basaltic andesite to andesite in composition. Plagioclase and pyroxene phenocrysts and matrix crystals in the central facies show unusually large compositional ranges and complex textural relationships. Whole-rock major and trace-element abundances show linear variations against MgO content, consistent with the rocks in the central facies having formed by mixing of basalt and rhyolite magmas. The rhyolite can be closely matched by rocks from the Mull centre. The mafic and silicic magmas were intruded from a compositionally zoned chamber beneath Mull, perhaps during collapse of the Centre 1 caldera. The lower-viscosity basaltic magma was emplaced before, but lubricated the lateral propagation of, the silicic magma, which mixed with the partially solidified basalt, the proportion of rhyolite increasing towards the dyke centre. The Eskdalemuir dyke represents an unusual, perhaps unique, example of a rhyolite magma being emplaced >200 km from its inferred source. The supposed correlative of the Eskdalemuir dyke north of the Southern Uplands Fault, the Dalraith-Linburn dyke, is not comagmatic with it.

Hydrothermal alteration of chevkinite-group minerals. Part 2. Metasomatite from the Keivy massif, Kola Peninsula, Russia

Abstract Chevkinite-(Ce) in a mineralized quartz-epidote metasomatite from the Keivy massif, Kola Peninsula, Russia, underwent at least two stages of low-temperature alteration. In the first, it interacted with hydrothermal fluids, with loss of Ca, Fe, LREE and Si and strong enrichment in Ti. The altered chevkinite was then rimmed and partially replaced by a zone of ferriallanite-(Ce) and davidite-(La), in turn rimmed by a zone of allanite-(Ce) richer in the epidote component. The allanite zone was in turn partially replaced by rutile-titanite-quartz assemblages, the formation of titanite postdating that of rutile. Aeschynite-(Y), aeschynite-(Ce) and REE-carbonates are accessory phases in all zones. The hydrothermal fluids were alkaline, with significant proportions of CO2 and F. At various alteration stages, the Ca, Si ± Al activities in the fluid were high. Formation of the aeschynite is discussed in relation to its stability in broadly similar parageneses; it was a primary phase in the unaltered chevkinite zone whereas in other zones it formed from Nb, Ti, REE and Th released from the major phases.

Low-temperature zircon growth related to hydrothermal alteration of siderite concretions in Mississippian shales, Scotland

Zircon occurs in voids and cracks in phosphatic coprolites enclosed in siderite concretions in Mississippian shales near Edinburgh, Scotland. The zircon formed during hydrothermal alteration of early-diagenetic concretions and occurs as spherical aggregates of prismatic crystals, sometimes radiating. Vitrinite reflectance measurements indicate temperatures of ~270°C for the zircon-bearing concretions and the host shales. Molecular parameter values based on dibenzothiophene and phenanthrene distribution and occurrence of di- and tetra-hydro-products of polycyclic aromatic compounds suggest that the rocks experienced relatively high-temperature aqueous conditions related to hydrothermal fluids, perhaps associated with neighboring mafic intrusions. The zircon was dissolved from the concretions, transported in fluids, and reprecipitated in voids. This is the first record of the precipitation of authigenic zircon in sedimentary rock as a new phase, not as outgrowths.

Complex relationships among coexisting pyroxenes: the Palaeogene Eskdalemuir dyke, Scotland

Abstract The composite Eskdalemuir dyke was formed by the intrusion of rhyolitic magma into partly crystallized basaltic magma, the proportion of the silicic component increasing towards the dyke centre. The less silicic parts were effectively supercooled and crystallization was halted when the residual melt quenched to rhyolitic glass which constitutes up to 50% of the dyke’s centre. Pyroxene compositions in the mixed magma rocks include augite, pigeonite and orthopyroxene of very variable composition. Individual crystals in the matrix as small as 200 μm can contain compositions occupying a considerable part of the Di-Hd-En-Fs quadrilateral. Pyroxene crystallization took place under extreme disequilibrium conditions, as shown by highly variable zonation patterns; apparently opposite zoning trends can occur in adjacent grains. Small-scale variations in melt composition were probably the dominant control over the compositional and textural complexity in the pyroxenes.

Hydrothermal alteration of chevkinite-group minerals: products and mechanisms. Part 1. Hydration of chevkinite-(Ce)

Abstract Samples from Russia and Scotland are used to examine the interaction of the REE-Ti silicate chevkinite-(Ce) with hydrothermal fluids. Altered zones in crystals are distinguished by using areas of low intensity on backscattered-electron images, low analytical totals, increasingly large departures from stoichiometry and, in some cases, the presence of micropores. Initial alteration of the chevkinite results in strong Ca enrichment. With increasing degrees of alteration, Ca abundances drop sharply, as do those of the REE, Fe and Si. In contrast, Ti levels increase strongly, usually accompanied by higher Nb ± Th levels. The most altered zones contain up to 36 wt.% TiO2 and the formula cannot be expressed in the standard chevkinite formula. In detail, samples follow different alteration trends, presumably reflecting different P, T, fO₂ and fluid composition. The Ti enrichment may have been related to a reaction front of dissolution-reprecipitation passing through the outer zones of the original chevkinite, leaving behind a reprecipitated Ti-enriched phase which may or may not be chevkinite.