Tectono-magmatic evolution of the younger Gardar southern rift, South Greenland

The 1300–1140 Ma Gardar period in South Greenland involved continental rifting, sedimentation and alkaline magmatism. The latest magmatism was located along two parallel rift zones, Isortoq–Nunarsuit in the north and the Tuttutooq–Ilimmaasaq–Narsarsuaq zone in the south addressed here. The intrusive rocks crystallised at a depth of troctolitic gabbros. These relatively reduced magmas evolved through marked iron enrichment to alkaline salic differentiates. In the Older giant dyke complex, undersaturated augite syenites grade into sodalite foyaite. The larger, c. 1163 Ma Younger giant dyke complex (YGDC) mainly consists of structureless troctolite with localised developments of layered cumulates. A layered pluton (Klokken) is considered to be coeval and presumably comagmatic with the YGDC. At the unconformity between the Ketilidian basement and Gardar rift deposits, the YGDC expanded into a gabbroic lopolith. Its magma may represent a sample from a great, underplated mafic magma reservoir, parental to all the salic alkaline rocks in the southern rift. The bulk of these are silica undersaturated; oversaturated differentiates are probably products of combined fractional crystallisation and crustal assimilation. A major dyke swarm 1–15 km broad was intruded during declining crustal extension, with decreasing dyke widths and increasing differentiation over time. Intersection of the dyke swarm and E–W-trending sinistral faults controlled the emplacement of at least three central complexes (Narssaq, South Qôroq and early Igdlerfigssalik). Three post-extensional complexes (Tugtutôq, Ilímaussaq and late Igdlerfigssalik) along the former rift mark the end of magmatism at c. 1140 Ma. The latter two complexes have oblate plans reflecting ductile, fault-related strain. The Tugtutôq complex comprises quartz syenites and alkali granites. The Ilímaussaq complex mainly consists of nepheline syenite crystallised from highly reduced, Fe-rich phonolitic peralkaline (agpaitic) magma, and resulted in rocks with very high incompatible element concentrations. Abundant anorthositic xenoliths in the mafic and intermediate intrusions point to a large anorthosite protolith at depth which is considered of critical importance in the petrogenesis of the salic rocks. Small intrusions of aillikite and carbonatite may represent remobilised mantle metasomites. The petrological similarity between Older and Younger Gardar suites implies strong lithospheric control of their petrogenesis. The parental magmas are inferred to have been derived from restitic Ketilidian lithospheric mantle, metasomatised by melts from subducting Ketilidian oceanic crust and by small-scale melt fractions associated with Gardar rifting. There are numerous analogies between the southern Gardar rift and the Palaeogene East African rift

Origin of mafic and ultramafic cumulates from the Ditrău Alkaline Massif, Romania

Mafic–ultramafic cumulates enclosed in gabbroic-dioritic rocks form part of the Mesozoic Ditrău Alkaline Massif in the Eastern Carpathians, Romania. The poikilitic olivine- and pyroxene-rich and nearly mono mineralic hornblendite rocks display typical cumulate textures with early crystallised olivine (Fo75–73), diopside and augite. In the early stages of their genesis the amphibole was intercumulus whilst in later stages it acquired cumulus status as the fractionating magma evolved. Using major and trace element compositions of minerals and whole-rock samples the origin of these cumulates is determined and the parental magma composition and depth of emplacement are calculated. Cumulus clinopyroxene has more primitive composition than intercumulus amphibole suggesting closed system fractionation for the evolution of poikilitic olivine- and pyroxene-rich cumulates. The evolution of the amphibole-rich mesocumulates is more clearly the result of closed system crystallisation dominated by the precipitation of clinopyroxene and amphibole cumulus crystals. Lamprophyre dykes of the Ditrău Alkaline Massif are proposed to reflect multiple basanitic parental magma batches from which the cumulus olivine and clinopyroxene crystallised. Relative to these dykes the calculated equilibrium melts for intercumulus amphibole in the cumulates was more primitive whilst that for the cumulus amphibole was more evolved. The calculated crystallisation temperature and pressure of ~1000–1050 °C and ~0.7 GPa, based on the composition of the amphiboles, indicate crystallisation at lower crustal depths. Rare earth element compositions are consistent with an intra-plate tectonic setting

Mantle sources and magma evolution in Europe's largest rare earth element belt (Gardar Province, SW Greenland) : new insights from sulfur isotopes

This work is a contribution to the HiTech AlkCarb project and was funded by the European Union's Horizon 2020 research and innovation programme under grant agreement No. 689909. W.H. also acknowledges support from a UKRI Future Leaders Fellowship (MR/S033505/1). A.J.B. is funded by the NERC National Environment Isotope Facility award (NE/S011587/1) and the Scottish Universities Environmental Research Centre.Alkaline igneous complexes are often rich in rare earth elements (REE) and other metals essential for modern technologies. Although a variety of magmatic and hydrothermal processes explain the occurrence of individual deposits, one common feature identified in almost all studies, is a REE-enriched parental melt sourced from the lithospheric mantle. Fundamental questions remain about the origin and importance of the mantle source in the genesis of REE-rich magmas. In particular, it is often unclear whether localized enrichments within an alkaline province reflect heterogeneity in the mantle source lithology (caused by prior subduction or plume activity) or variations in the degree of partial melting and differentiation of a largely homogeneous source. Sulfur isotopes offer a means of testing these hypotheses because they are unaffected by high temperature partial melting processes and can fingerprint different mantle sources. Although one must be careful to rule out subsequent isotope fractionation during magma ascent, degassing and crustal interactions. Here, we present new S concentration and isotope (δ34S) measurements, as well as a compilation of major and trace element data, for a suite of alkaline magmatic units and crustal lithologies from the Mesoproterozoic Gardar Province. Samples span all phases of Gardar magmatism (1330–1140 Ma) and include regional dykes, rift lavas and the alkaline complexes Motzfeldt and Ilímaussaq, which represent two of Europe's largest REE deposits. We show that the vast majority of our 115 samples have S contents >100 ppm and δ34S of −1 to 5‰. Only 8 samples (with low S contents, <100 ppm) show evidence for crustal interactions, implying that the vast majority of Gardar melts preserve the S isotopic signature of their magma source. Importantly, samples from across the Gardar Province δ34S have above the canonical mantle range (≤−1.4‰) and therefore require recycled surface S in their mantle source. Elevated values are explained by a period of Andean-style subduction and mantle metasomatism which took place ∼500 Ma before rift onset and are also supported by trace elements signatures (e.g. Ba/La) which match modern subduction zones. Comparing the various generations of Gardar magmas, we find that δ34S  values, large ion lithophile elements (K, Ba, P) and selective incompatible elements (Nb and light REE) are particularly enriched in the Late Gardar dykes, alkaline complexes and clusters of silica-undersaturated dykes spatially associated with the alkaline complexes. These data indicate that subduction-related metasomatism of the Gardar mantle was spatially heterogeneous, and that alkaline complexes are sourced from localized mantle domains highly enriched in 34S, REE, alkalis and volatiles (particularly, F). Since alkalis and volatiles play an essential role in driving extreme differentiation of alkaline melts and fluids, we suggest the co-location of these species plus incompatible metals at high concentrations in the lithospheric mantle is a critical first-step in the genesis of a world-class alkaline REE deposit. S isotopes are powerful tools for identifying enriched mantle domains and the sources of mineralized alkaline igneous bodies.Publisher PDFPeer reviewe

Paradoxical co-existing base metal sulphides in the mantle: The multi-event record preserved in Loch Roag peridotite xenoliths, North Atlantic Craton

The role of the subcontinental lithospheric mantle as a source of precious metals for mafic magmas is contentious and, given the chalcophile (and siderophile) character of metals such as the platinum-group elements (PGE), Se, Te, Re, Cu and Au, the mobility of these metals is intimately linked with that of sulphur. Hence the nature of the host phase(s), and their age and stability in the subcontinental lithospheric mantle may be of critical importance. We investigate the sulphide mineralogy and sulphide in situ trace element compositions in base metal sulphides (BMS) in a suite of spinel lherzolite mantle xenoliths from northwest Scotland (Loch Roag, Isle of Lewis). This area is situated on the margin of the North Atlantic Craton which has been overprinted by a Palaeoproterozoic orogenic belt, and occurs in a region which has undergone magmatic events from the Palaeoproterozoic to the Eocene. We identify two populations of co-existing BMS within a single spinel lherzolite xenolith (LR80) and which can also be recognised in the peridotite xenolith suite as a whole. Both populations consist of a mixture of Fe-Ni-Cu sulphide minerals, and we distinguished between these according to BMS texture, petrographic setting (i.e., location within the xenolith in terms of ‘interstitial’ or within feldspar-spinel symplectites, as demonstrated by X-ray Computed Microtomography) and in situ trace element composition. Group A BMS are coarse, metasomatic, have low concentrations of total PGE (&lt; 40 ppm) and high (Re/Os)N (ranging 1 to 400). Group B BMS strictly occur within symplectites of spinel and feldspar, are finer-grained rounded droplets, with micron-scale PtS (cooperite), high overall total PGE concentrations (15–800 ppm) and low (Re/Os)N ranging 0.04 to 2. Group B BMS sometimes coexist with apatite, and both the Group B BMS and apatite can preserve rounded micron-scale Ca-carbonate inclusions indicative of sulphide-carbonate-phosphate immiscibility. This carbonate-phosphate metasomatic association appears to be important in forming PGE-rich sulphide liquids, although the precise mechanism for this remains obscure. As a consequence of their position within the symplectites, Group B BMS are particularly vulnerable to being incorporated in ascending mantle-derived magmas (either by melting or physical entrainment). Based on the cross-cutting relationships of the symplectites, it is possible to infer the relative ages of each metasomatic BMS population. We tally these with major tectono-magmatic events for the North Atlantic region by making comparisons to carbonatite events recorded in crustal and mantle rocks, and we suggest that the Pt-enrichment was associated with a pre-Carboniferous carbonatite episode. This method of mantle xenolith base metal sulphide documentation may ultimately permit the temporal and spatial mapping of the chalcophile metallogenic budget of the lithospheric mantle, providing a blueprint for assessing regional metallogenic potential. Abbreviations: NAC, North Atlantic Craton; GGF, Great Glen Fault; NAIP, North Atlantic Igneous Province; BPIP, British Palaeogene Igneous Province; SCLM, subcontinental lithospheric mantle; PGE, platinum-group elements; HSE, highly siderophile elements; BMS, base metal sulphid

Cobalt and precious metals in sulphides of peridotite xenoliths and inferences concerning their distribution according to geodynamic environment: A case study from the Scottish lithospheric mantle

Abundances of precious metals and cobalt in the lithospheric mantle are typically obtained by bulk geochemical analyses of mantle xenoliths. These elements are strongly chalcophile and the mineralogy, texture and trace element composition of sulphide phases in such samples must be considered. In this study we assess the mineralogy, textures and trace element compositions of sulphides in spinel lherzolites from four Scottish lithospheric terranes, which provide an ideal testing ground to examine the variability of sulphides and their precious metal endowments according to terrane age and geodynamic environment. Specifically we test differences in sulphide composition from Archaean-Palaeoproterozoic cratonic sub-continental lithospheric mantle (SCLM) in northern terranes vs. Palaeozoic lithospheric mantle in southern terranes, as divided by the Great Glen Fault (GGF). Cobalt is consistently elevated in sulphides from Palaeozoic terranes (south of the GGF) with Co concentrations > 2.9 wt.% and Co/Ni ratios > 0.048 (chondrite). In contrast, sulphides from Archaean cratonic terranes (north of the GGF) have low abundances of Co (< 3600 ppm) and low Co/Ni ratios (< 0.030). The causes for Co enrichment remain unclear, but we highlight that globally significant Co mineralisation is associated with ophiolites (e.g., Bou Azzer, Morocco and Outokumpu, Finland) or in oceanic peridotite-floored settings at slow-spreading ridges. Thus we suggest an oceanic affinity for the Co enrichment in the southern terranes of Scotland, likely directly related to the subduction of Co-enriched oceanic crust during the Caledonian Orogeny. Further, we identify a distinction between Pt/Pd ratio across the GGF, such that sulphides in the cratonic SCLM have Pt/Pd ≥ chondrite whilst Palaeozoic sulphides have Pt/Pd < chondrite. We observe that Pt-rich sulphides with discrete Pt-minerals (e.g., PtS) are associated with carbonate and phosphates in two xenolith suites north of the GGF. This three-way immiscibility (carbonate-sulphide-phosphate) indicates carbonatitic metasomatism is responsible for Pt-enrichment in this (marginal) cratonic setting. These Co and Pt-enrichments may fundamentally reflect the geodynamic setting of cratonic vs. non-cratonic lithospheric terranes and offer potential tools to facilitate geochemical mapping of the lithospheric mantle

Ueber den Zusammenhang zwischen Jacobiformen und Modulformen halbganzen Gewichts

SIGLETIB: RA 224 (159) / FIZ - Fachinformationszzentrum Karlsruhe / TIB - Technische InformationsbibliothekDEGerman

The mantle of Scotland viewed through the Glen Gollaidh aillikite

The Glen Gollaidh aillikite dyke (58.36741°N 4.69751°W), N.W. Scotland, occurs within the Neoproterozoic sedimentary rocks of the Moine Supergroup ~4 km east of the Moine Thrust. Phlogopite 40Ar/36Ar measurements give a late Devonian maximum emplacement age of 360.3 ± 4.9 (2σ) Ma. This age occurs in a quiet period of Scottish magmatic history c. 30 Ma after the closure of the Iapetus and before the start of intra-plate alkali magmatism which affected southern Scotland for ~60 My from c. 350 Ma. Abundant chromites and Cr-diopsides and a few unaltered olivines, reflecting a mantle provenance, were recovered from heavy mineral concentrates. The North Atlantic Craton, exposed in Lewisian gneisses west of the Moine thrust, is therefore inferred to extend east at depth under Glen Gollaidh, presenting an opportunity to investigate the thickness and composition of the cratonic margin in the Devonian. The aillikite was found to be barren of diamond and no picro-ilmenites or garnets were definitively identified. However, mineral chemistry suggests that a proportion of Glen Gollaidh xenocrysts crystallised in equilibrium with garnet. Most spinels are Mg, Al chromites, with some Mg chromite present. All fall within the garnet peridotite field based on Ti and Cr but with insufficient Cr2O3 (up to 47.2 wt%) to be consistent with the diamond stability field. Amongst Cr-diopsides 30% of grains have Cr and Al contents consistent with derivation from garnet peridotite. The majority of clinopyroxenes also show a marked depletion in heavy compared to light rare-earth elements, again consistent with equilibration with garnet. The opx-cpx solvus thermometer demonstrates that average Cr-diopside compositions require at least 37 kbar to give a temperature (979 °C) lying even on a relatively warm 40 mWm−2 geotherm (Hasterok and Chapman Earth Planet Sc Lett 307:59–70, 2011). Large variations in the chemistry of mantle minerals reflect a complex history of metasomatism akin to constituents of alkali igneous rocks elsewhere in the Hebridean and Northern Highlands Terranes. Fertilised mantle provided the conditions for generation of aillikite melts, probably triggered by break-off of the advancing Avalonia slab. The cratonic root underlying the Glen Gollaidh aillikite during the late Devonian was apparently too thin to lie within the diamond stability field, consistent with xenoliths from alkali basalts further south. Nonetheless, sufficient geophysical and mineral chemical evidence supports Glen Gollaidh aillikite sitting close to the edge of diamond-prospective mantle therefore suggesting diamond potential a short distance to the west within the Lewisian and what is now East Greenland

The peridotite plugs of Rum: Crystal settling and fabric development in magma conduits

The Rum Igneous Complex contains numerous circular to elongate exposures of peridotite cumulates within the layered series and the country rock. The extent of thermal effects on quartzo-feldspathic country rock surrounding the Mam Tuath and West Sgaorishal plugs demonstrates that these are pipe-like bodies, inclined at various angles to the vertical, that remained at magmatic temperatures for periods of up to several months. Tabular olivine grains within the plugs preserve a weak sub-horizontal fabric that is stronger in the plug centres than at their margins. The olivine mode increases from ~&#xa0;50&#xa0;vol.% at the plug margins to ~&#xa0;85&#xa0;vol.% at the centre. The spatial arrangement of the olivine grains is consistent with their being clustered, with the increase in mode towards the plug centres achieved by a combination of overgrowth and mechanical re-arrangement. Comparison of fabrics with those of the Ard Mheall peridotites of the Rum Western Layered Intrusion is consistent with porosity reduction in the Ard Mheall cumulates also having been primarily achieved by overgrowth and mechanical re-arrangement: compaction via intra-crystalline deformation did not occur. We suggest that the Rum ultramafic plugs are deep-level cross-sections presenting the ultimate ‘snap-shots’ of volcanic conduits through which olivine-rich magmas flowed for substantial periods, probably giving rise to fire-fountains of the kind associated with Hawaiian eruptions. The exposed parts of the plugs are now miniature cumulate bodies that developed in situ from the settling of olivine phenocrysts once flow had ceased within the conduit