Poles apart: A discussion of “Geochemistry of cumulates from the Bjerkreim–Sokndal Intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent” by J.C. Duchesne and B. Charlier (Lithos 83, 2005, 229–254)

We dispute Duchesne and Charlier's (Duchesne, J.C., Charlier, B., 2005. Geochemistry of cumulates from the Bjerkreim–Sokndal Intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent. Lithos 83, 229–254.) postulate that the major-element compositions of cumulates in the Bjerkreim–Sokndal Intrusion vary linearly between plagioclase and mafic “poles” and their inference that this supports an origin by in situ crystallisation. We use a larger set of major-element data for plagioclase–orthopyroxene–ilmenite cumulates to show that some linear trends in Harker diagrams simply reflect varying amounts of hemo-ilmenite relative to plagioclase and orthopyroxene, while others are probably spurious and induced by variations in modal plagioclase, the most abundant cumulus mineral. Ratios of oxides that enter almost exclusively into orthopyroxene and hemo-ilmenite are shown to be highly dispersed, reflecting differential sorting of the mafic minerals.     

Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway). Part I: Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent

Whole-rock major element compositions are investigated in 99 cumulates from the Proterozoic Bjerkreim–Sokndal layered intrusion (Rogaland Anorthosite Province, SW Norway), which results from the crystallization of a jotunite (Fe–Ti–P-rich hypersthene monzodiorite) parental magma. The scattering of cumulate compositions covers three types of cumulates: (1) ilmenite–leuconorite with plagioclase, ilmenite and Ca-poor pyroxene as cumulus minerals, (2) magnetite–leuconorite with the same minerals plus magnetite, and (3) gabbronorite made up of plagioclase, Ca-poor and Ca-rich pyroxenes, ilmenite, Ti-magnetite and apatite. Each type of cumulate displays a linear trend in variation diagrams. One pole of the linear trends is represented by plagioclase, and the other by a mixture of the mafic minerals in constant proportion. The mafic minerals were not sorted during cumulate formation though they display large density differences. This suggests that crystal settling did not operate during cumulate formation, and that in situ crystallization with variable nucleation rate for plagioclase was the dominant formation mechanism. The trapped liquid fraction of the cumulate plays a negligible role for the cumulate major element composition. Each linear trend is a locus for the cotectic composition of the cumulates. This property permits reconstruction by graphical mass balance calculation of the first two stages of the liquid line of descent, starting from a primitive jotunite, the Tjörn parental magma. Another type of cumulate, called jotunite cumulate and defined by the mineral association from the Transition Zone of the intrusion, has to be subtracted to simulate the most evolved part of the liquid line of descent. The proposed model demonstrates that average cumulate compositions represent cotectic compositions when the number of samples is large (> 40). The model, however, does not account for the K₂O evolution, suggesting that the system was open to contamination by roof melts. The liquid line of descent corresponding to the Bjerkreim–Sokndal cumulates differs slightly from that obtained for jotunitic dykes in that the most Ti-, P- and Fe-rich melts (evolved jotunite) are lacking. The constant composition of the mafic poles during intervals where cryptic layering is conspicuous is explained by a compositional balance between the Fe–Ti oxide minerals, which decrease in Fe content in favour of Ti, and the pyroxenes which increase in Fe.     

Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway) Part II. REE and the trapped liquid fraction

Rare earth elements in bulk cumulates and in separated minerals (plagioclase, apatite, Ca-poor and Ca-rich pyroxenes, ilmenite and magnetite) from the Bjerkreim–Sokndal layered intrusion (Rogaland Anorthosite Province, SW Norway) are investigated to better define the proportion of trapped liquid and its influence on bulk cumulate composition. In leuconoritic rocks (made up of plagioclase, Ca-poor pyroxene, ilmenite, ±magnetite, ±olivine), where apatite is an intercumulus phase, even a small fraction of trapped liquid significantly affects the REE pattern of the bulk cumulate, together with cumulus minerals proportion and composition. Contrastingly, in gabbronoritic cumulates characterized by the presence of cumulus Ca-rich pyroxene and apatite, cumulus apatite buffers the REE content. La/Sm and Eu/Eu* vs. P₂O₅ variations in leuconorites display mixing trends between a pure adcumulate and the composition of the trapped liquid, assumed to be similar to the parental magma. Assessment of the trapped liquid fraction in leuconorites ranges from 2 to 25% and is systematically higher in the north-eastern part of the intrusion. The likely reason for this wide range of TLF is different cooling rates in different parts of the intrusion depending on the distance to the gneissic margins. The REE patterns of liquids in equilibrium with primitive cumulates are calculated with mass balance equations. Major elements modelling (Duchesne, J.C., Charlier, B., 2005. Geochemistry of cumulates from the Bjerkreim–Sokndal layered intrusion (S. Norway): Part I. Constraints from major elements on the mechanism of cumulate formation and on the jotunite liquid line of descent. Lithos. 83, 299–254) permits calculation of the REE content of melt in equilibrium with gabbronorites. Partition coefficients for REE between cumulus minerals and a jotunitic liquid are then calculated. Calculated liquids from the most primitive cumulates are similar to a primitive jotunite representing the parental magma of the intrusion, taking into account the trapped liquid fraction calculated from the P₂O₅ content. Consistent results demonstrate the reliability of liquid compositions calculated from bulk cumulates and confirm the hypothesis that the trapped liquid has crystallized as a closed-system without subsequent mobility of REE in a migrating interstitial liquid.     

The Grader layered intrusion (Havre-Saint-Pierre Anorthosite, Quebec) and genesis of nelsonite and other Fe–Ti–P ores

The Grader layered intrusion is part of the Havre-Saint-Pierre anorthosite in the Grenville Province (Quebec, Canada). This intrusion has a basin-like morphology and contains significant resources of Fe–Ti–P in ilmenite and apatite. Outcropping lithologies are massive oxide alternating with anorthosite layers, banded ilmenite–apatite–plagioclase rocks and layered oxide apatite (gabbro-)norites. Drill cores provide evidence for stratigraphic variations of mineral and whole rock compositions controlled by fractional crystallization with the successive appearance of liquidus phases: plagioclase and ilmenite followed by apatite, then orthopyroxene together with magnetite, and finally clinopyroxene. This atypical sequence of crystallization resulted in the formation of plagioclase–ilmenite–apatite cumulates or “nelsonites” in plagioclase-free layers. Fine-grained ferrodiorites that cross-cut the cumulates are shown to be in equilibrium with the noritic rocks. The high TiO₂ and P₂O₅ contents of these assumed liquids explains the early saturation of ilmenite and apatite before Fe–Mg silicates, thus the nelsonites represent cumulates rather than crystallized Fe–Ti–P-rich immiscible melts. The location of the most evolved mineral and whole rock compositions several tens of meters below the top of the intrusion, forming a sandwich horizon, is consistent with crystallization both from the base and top of the intrusion. The concentrations of V and Cr in ilmenite display a single fractionation path for the different cumulus assemblages and define the cotectic proportion of ilmenite to 21 wt.%. This corresponds to bulk cotectic cumulates with ca. 8 wt.% TiO₂, which is significantly lower than what is commonly observed in the explored portion of the Grader intrusion. The proposed mechanism of ilmenite-enrichment is the lateral removal of plagioclase due to its relative buoyancy in the dense ferrodiorite melt. This plagioclase has probably accumulated in other portions of the intrusion or has not been distinguished from the host anorthosite.     

The Fedorivka layered intrusion (Korosten Pluton, Ukraine): An example of highly differentiated ferrobasaltic evolution

This study documents the petrography and whole-rock major and trace element geochemistry of 38 samples mainly from a drill core through the entire Fedorivka layered intrusion (Korosten Pluton), as well as mineral compositions (microprobe analyses and separated mineral fraction analyses of plagioclase, ilmenite, magnetite and apatite) of 10 samples. The Fedorivka layered intrusion can be divided into 4 lithostratigraphic units: a Lower Zone (LZ, 72 m thick), a Main Zone (MZ, 160 m thick), and an Upper Border Zone, itself subdivided into 2 sub-zones (UBZ₂, 40 m thick; UBZ₁, 50 m thick). Igneous lamination defines the cumulate texture, but primary cumulus minerals have been affected by trapped liquid crystallization and subsolidus recrystallization. The dominant cumulus assemblage in MZ and UBZ₂ is andesine (An_39–42), iron-rich olivine (Fo_32–42), augite (En_29–35Fs_24–29Wo_42–44), ilmenite (Hem_1–6), Ti-magnetite (Usp_52–78), and apatite. The data reveal a continuous evolution from the floor of the intrusion (LZ) to the top of MZ, due to fractional crystallization, and an inverse evolution in UBZ, resulting from crystallization downwards from the roof. The whole-rock Fe/Mg ratio and incompatible element contents (e.g. Rb, Nb, Zr, REE) increase in the fractionating magma, whereas compatible elements (e.g. V, Cr) steadily decrease. The intercumulus melt remained trapped in the UBZ cumulates due to rapid cooling and lack of compaction, and cumulus mineral compositions re-equilibrated (e.g. olivine, Fe–Ti oxides). In LZ, the intercumulus melt was able to partially or totally escape. The major element composition of the MZ cumulates can be approximated by a mixing (linear) relationship between a plagioclase pole and a mafic pole, the latter being made up of all mafic minerals in (nearly) constant relative proportions. By analogy with the ferrobasaltic/jotunitic liquid line of descent, defined in Rogaland, S. Norway, and its conjugated cumulates occurring in the Transition Zone of the Bjerkreim-Sokndal intrusion (Rogaland, a monzonitic (57% SiO₂) melt is inferred to be in equilibrium with the MZ cumulates. The conjugated cumulate composition falls (within error) on the locus of cotectic compositions fixed by the 2-pole linear relationship. Ulvöspinel is the only Ti phase in some magnetites that have been protected from oxidation. QUIlF equilibria in these samples show that magnetite and olivine in MZ have retained their liquidus compositions during subsolidus cooling. This permits calculation of liquidus fO₂ conditions, which vary during fractionation from ΔFMQ = 0.7 to − 1.4 log units. Low fO₂ values are also evidenced by the late appearance of cumulus magnetite (Fo₄₂) and the high V³⁺-content of the melt, reflected in the high V-content of the first liquidus magnetite (up to 1.85% V).     

The Apophysis of the Bjerkreim–Sokndal layered intrusion (Rogaland anorthosite province, SW Norway): A composite pluton build up by tectonically-driven emplacement of magmas along the margin of an AMC igneous complex

The Late-Proterozoic Bjerkreim–Sokndal layered intrusion (BKSK) is connected to a foliated, sheet-like igneous body (the Apophysis), that is a potential feeder for the BKSK magma chamber. Field, petrographical, geochemical and structural data are used to demonstrate that the Apophysis is a composite igneous body, constructed by coeval mafic to felsic magmas that were collected in a sub-vertical shear zone. Three liquid lines of descent are distinguished in the main Apophysis component (a felsic series, predominantly quartz mangeritic) and in coeval felsic rocks from the upper part of the BKSK. Minor mineralogical and geochemical discrepancies between these three trends are indicative of distinct sources and crustal contaminants, as well as slight differences in the differentiation mechanisms. Jotunitic to noritic cumulates or crystal-laden magmas, associated with their trapped melts, mingled with the felsic series in two distinct portions of the Apophysis. In one area, this association is dominated by a FTP (Fe–Ti–P-rich) jotunite, interpreted as an accumulation of pyroxenes + Fe – Ti oxides + apatite + plagioclase. In the second area, the melt dominates over the associated cumulate; it is a primitive (MgO-rich and K₂O-poor) jotunite, that was also involved in the genesis of another igneous body in the vicinity of the Apophysis. Magma mixing, in addition to mingling, was also potentially important in the petrogenesis of some jotunite rocks.     

Modification of the subcontinental mantle beneath East Serbia: Evidence from orthopyroxene-rich xenoliths

Orthopyroxene-rich olivine websterite xenoliths (OWB₂) in Palaeogene basanites in East Serbia are mostly composed of tabular low-Al₂O₃ orthopyroxene (> 70 vol.%, Mg# 85–87) containing tiny Cr spinel inclusions. Orthopyroxene shows a slightly U-shaped primitive mantle-normalized trace element pattern with strong peaks at U and Pb, similar to that of orthopyroxene from normal regional peridotitic mantle. In between the orthopyroxenes are interstitial spaces composed of partially altered olivine (Mg# 85–87), clinopyroxene, Ti-rich spinel, Mg-bearing calcite, K-feldspar, apatite, ilmenite and relicts of a hydrous mineral. Clinopyroxene appears as selvages around orthopyroxene and as coarser euhedral crystals. Trace element patterns of the clinopyroxene selvages resemble those of adjacent orthopyroxene, whereas the coarser ones have flatter and more LREE- and LILE-enriched patterns, similar to that of metasomatic clinopyroxene. The OWB₂ xenoliths are interpreted as having formed in two stages. During Stage I orthopyroxene crystallized, along with some spinel, olivine and probably hydrous phase(s). This original OWB₂ lithology was a hydrous olivine-bearing orthopyroxenite that crystallised from subduction-related SiO₂-saturated, boninite-like magmas. During Stage II the interstitial minerals formed due to infiltration of a low-SiO₂, high-CaO and CO₂-rich external melt, accompanied by decomposition of original H₂O-bearing minerals. The calculated composition of the infiltrating liquid corresponds to a mafic alkaline melt similar to the basanitic host but more enriched in CO₂, LREE and LILE. Metasomatism is interpreted in terms of small degree melts related to the Palaeogene mafic alkaline magmatism.     

The Asama igneous complex, central Japan: An ultramafic-mafic layered intrusion in the Mikabu greenstone belt, Sambagawa metamorphic terrain

The Asama igneous complex comprises layered mafic and ultramafic plutonic rocks exposed over about 500×6000 m in the Mikabu greenstone belt, Sambagawa metamorphic terrain of Mie Prefecture; its margins terminate by faults, and there is no trace of chilled rocks. The exposed layered sequence is about 460 m thick, and includes dunite, plagioclase wehrlite, olivine gabbro and two-pyroxene gabbro. The crystallization sequence of essential cumulus minerals is olivine, followed by plagioclase and clinopyroxene together, and finally the appearance of orthopyroxene. Olivine systematically varies in composition from Fo₈₉ to Fo₇₈ with stratigraphic height in the lower to middle portion of the layered sequence. The composition of clinopyroxene changes from Ca₄₉Mg₄₆Fe₅ to Ca₄₀Mg₄₇Fe₁₃ upward in the layered sequence; cumulus orthopyroxene, which occurs at the top of the exposed layered sequence, has a composition of Ca₂Mg₇₄Fe₂₄. Cumulus chromite occurs as disseminated grains in peridotitic rocks, and tends to increase its Fe³⁺/(Cr+Al+Fe³⁺) ratio with stratigraphic height. The most aluminous chromite [Cr/(Cr+Al) = 0.48] occurs in dunite that crystallized shortly before plagioclase began to separate as an essential phase. The Cr/(Cr+Al) ratio of the most aluminous chromite, coupled with the crystallization order of essential minerals, suggests that the Asama parental magma was moderately enriched in plagioclase and clinopyroxene components in the normative mineral diagram plagioclase-clinopyroxene-orthopyroxene. It was similar to a Hawaiian tholeiite and different from the Bushveld and Great “Dyke” parental magmas that were more enriched in orthopyroxene component; it also differed from mid-oceanic ridge basalts that are more depleted in the orthopyroxene component. The Asama clinopyroxene and chromite show characteristically high TiO₂ contents and are also similar to those in Hawaiian tholeiites. The Asama igneous complex probably resulted from the crystallization of a magma of a Hawaiian (oceanic-island) tholeiite composition and formed in an oceanic island regime.     

The origin of garnet and clinopyroxene in “depleted” Kaapvaal peridotites

A detailed petrographic, major and trace element and isotope (Re–Os) study is presented on 18 xenoliths from Northern Lesotho kimberlites. The samples represent typical coarse, low-temperature garnet and spinel peridotites and span a P–T range from 60 to 150 km depth. With the exception of one sample (that belongs to the ilmenite–rutile–phlogopite–sulphide suite (IRPS) suite first described by [B. Harte, P.A. Winterburn, J.J. Gurney, Metasomatic and enrichment phenomena in garnet peridotite facies mantle xenoliths from the Matsoku kimberlite pipe, Lesotho. In: Menzies, M. (Ed.), Mantle metsasomatism. Academic Press, London 1987, 145–220.]), all samples considered here have high Mg# and show strong depletion in CaO and Al₂O₃. They have bulk rock Re depletion ages (T_RD) >2.5 Ga and are therefore interpreted as residua from large volume melting in the Archaean. A characteristic of Kaapvaal xenoliths, however, is their high SiO₂ concentrations, and hence, modal orthopyroxene contents that are inconsistent with a simple residual origin of these samples. Moreover, trace element signatures show strong overall incompatible element enrichment and REE disequilibrium between garnet and clinopyroxene. Textural and subtle major element disequilibria were also observed. We therefore conclude that garnet and clinopyroxene are not co-genetic and suggest that (most) clinopyroxene in the Archaean Kaapvaal peridotite xenoliths is of metasomatic origin and crystallized relatively recently, possibly from a melt precursory to the kimberlite.

Possible explanations for the origin of garnet are exsolution from a high-temperature, Al- and Ca-rich orthopyroxene (indicating primary melt extraction at shallow levels) or a majorite phase (primary melting at >6 GPa). Mass balance calculations, however, show that not all garnet observed in the samples today is of a simple exsolution origin. The extreme LREE enrichment (sigmoidal REE pattern in all garnet cores) is also inconsistent with exsolution from a residual orthopyroxene. Therefore, extensive metasomatism and probably re-crystallization of the lithosphere after melt-depletion and garnet exsolution is required to obtain the present textural and compositional features of the xenoliths. The metasomatic agent that modified or perhaps even precipitated garnet was a highly fractionated melt or fluid that might have been derived from the asthenosphere or from recycled oceanic crust. Since, to date, partitioning of trace elements between orthopyroxene and garnet/clinopyroxene is poorly constrained, it was impossible to assess if orthopyroxene is in chemical equilibrium with garnet or clinopyroxene. Therefore, further trace element and isotopic studies are required to constrain the timing of garnet introduction/modification and its possible link with the SiO₂ enrichment of the Kaapvaal lithosphere.     

Vermicular orthopyroxene-magnetite symplectites from the Wateranga layered mafic intrusion,Queensland, Australia

Orthopyroxene-magnetite intergrowths (symplectites), partly or completely surrounding olivine, are described from the Wateranga layered mafic intrusion, Queensland, Australia. The texture occurs in unmetamorphosed plagioclase-rich norites, olivine gabbros and troctolites in which the primary minerals are olivine (Fo_63–69) orthopyroxene (En_66–72), clinopyroxene (Wo₄₂En₄₂Fs₁₆), plagioclase (An_49–65), hornblende, ilmenite, magnetite and sulphides. Symplectites range from incipient fine grained developments around corroded olivine grains to intricately formed pseudomorphs after olivine and slow a consistent orthopyroxene/magnetite ratio. Orthopyroxene in symplectites is commonly in optical continuity with surrounding magnetite-free orthopyroxene rims. Later intercumulus hornblended has replaced orthopyroxene. There is marked chemical similarity between primary and simplectite, orthopyroxenes and magnetites. Textures similar to those described here are considered elsewhere to have formed at a late magmatic stage or by solid state reactions involving subsolidus oxidation of olivine. In the Wateranga intrusion textural relations, the chemical similarity between primary and symplectite phases, and the consistent volume proportions of magnetite and orthopyroxene in the intergrowths suggest that they developed during late magmatic crystallization.     

Isotopic (O, Sr, Nd) and trace element geochemistry of the Laouni layered intrusions (Pan-African belt, Hoggar, Algeria): evidence for post-collisional continental tholeiitic magmas variably contaminated by continental crust

The three layered intrusions studied in the Laouni area have been emplaced within syn-kinematic Pan-African granites and older metamorphic rocks. They have crystallized at the end of the regional high-temperature metamorphism, but are free from metamorphic recrystallization, revealing a post-collisional character. The cumulate piles can be interpreted in terms of two magmatic liquid lines of descent: one is tholeiitic and marked by plagioclase–olivine–clinopyroxene cumulates (troctolites or olivine bearing gabbros), while the other is calc-alkaline and produced orthopyroxene–plagioclase rich cumulates (norites). One intrusion (WL (West Laouni)-troctolitic massif), shows a Lower Banded Zone where olivine-chromite orthocumulates are interlayered with orthopyroxene-rich and olivine–plagioclase–clinopyroxene cumulates, whereas the Upper Massive Zone consists mainly of troctolitic and gabbroic cumulates. The other two massifs are more homogeneous: the WL-noritic massif has a calc-alkaline differentiation trend whereas the EL (East Laouni)–troctolitic massif has a tholeiitic one. Separated pyroxene and plagioclase display similar incompatible trace element patterns, regardless of the cumulate type. Calculated liquids in equilibrium with the two pyroxenes for both noritic and troctolitic cumulates are characterized by negative Nb, Ta, Zr and Hf anomalies and light REE enrichment inherited from the parental magmas. Troctolitic cumulates have mantle-derived δ¹⁸O (+5 to +6‰), initial ⁸⁷Sr/⁸⁶Sr (Sr_i=0.7030 to 0.7054), _Nd (+5 to −1) values whereas noritic cumulates are variably enriched in δ¹⁸O (+7 to +9‰), show negative _Nd (−7 to −12) and slightly higher Sr_i (0.7040–0.7065). Based on field, isotopic ratios are interpreted as resulting from a depleted mantle source (Sr_i=0.7030; _Nd=+5.1; δ¹⁸O=+5.1‰) having experience short term incompatible element enrichment and variable crustal contamination. The mantle magma was slightly contaminated by an Archaean lower crust in troctolitic cumulates, more strongly and with an additional contamination by an Eburnian upper crust in noritic cumulates. Lower crust input is recorded mainly by Sr and Nd isotopes and upper crust input by O isotopes. This is probably due to the different water/rock ratios of these two crust types. Assimilation of low amounts (<10%) of quartz-bearing felsic rocks, coming from both lower and upper crust, can explain the rise of SiO₂ activity, the enrichment in ¹⁸O and ⁸⁷Sr and the lowering of _Nd in the noritic cumulates compared to troctolitic ones. The geodynamic model proposed to account for the Laouni tholeiitic magmatism involves a late Pan-African asthenospheric rise due to a rapid lithospheric thinning associated with functioning of shear zones, which allowed tholeiitic magmas to reach high crustal levels while experiencing decreasing degrees of crustal contamination with time.     

Marginal mafic intrusions as indicators of downslope draining of dense residual melts in anorthositic diapirs?

Geochemical and isotopic investigation of three small mafic intrusions (Løyning: 1250 × 150 m, Hogstad: 2000 × 200 m, Koldal: 1250 × 500 m) in the marginal zones of the Egersund-Ogna (Løyning, Koldal) and Åna-Sira massif-type anorthosites (Hogstad) (Rogaland Anorthositic Province, south Norway: 930 Ma) provides new insights into the late evolution of anorthositic diapirs. These layered mafic intrusions are essentially of norite, gabbronorite as well as leuconorite and display conspicuous evidence of subsolidus recrystallization. In Løyning and Hogstad, the modal layering is parallel to the subvertical foliation in the enclosing anorthosite. The northern part of the Koldal intrusion cuts across the foliation of the anorthosite, whereas in its southern part the subvertical layering is parallel to the anorthosite's foliation. The regularity of the layered structures suggests that the layering was initially acquired horizontally and later tilted during the final movements of the diapirs.

The least differentiated compositions of plagioclase and orthopyroxene in the three intrusions (An₅₉–En₆₈ in Løyning, An₄₉–En₆₄ in Hogstad and An₄₄–En₆₁ in Koldal) and the REE contents in apatite (Hogstad) indicate that their parent magmas were progressively more differentiated in the sequence Løyning–Hogstad–Koldal. Isotopic data (Løyning: ⁸⁷Sr/⁸⁶Sr: 0.70376–0.70457, ε_Ndt: + 6.8 to + 2.7; Hogstad: ⁸⁷Sr/⁸⁶Sr: 0.70537–0.70588, ε_Ndt: + 2.1 to − 0.5; Koldal: ⁸⁷Sr/⁸⁶Sr: 0.70659–0.70911, ε_Ndt: + 3.5 to − 1.6) also indicate that in this sequence, parent magmas were characterized by a progressively more enriched Sr and Nd isotopic signature. In Løyning, the parent magma was slightly more magnesian and anorthitic than a primitive jotunite; in Hogstad, it is a primitive jotunite; and, in Koldal, an evolved jotunite. Given that plagioclase and orthopyroxene of the three intrusions display more differentiated compositions than the orthopyroxene and plagioclase megacryts of the enclosing anorthosites, it is suggested that the parent magmas of the small intrusions are residual melts after anorthosite formation which were entrained in the anorthositic diapir during its rise from lower crustal chambers.

Calculated densities of primitive jotunites (2.73–2.74 at FMQ, 0.15% H₂O, 200 ppm CO₂, 435 ppm F, 1150 °C, 3 kb) and evolved jotunites (2.75–2.76 at FMQ, 0.30% H₂O, 400 ppm CO₂, 870 ppm F, 1135 °C, 3 kb) demonstrate that they are much denser than the plagioclase of the surrounding anorthositic crystal mush (2.61–2.65). Efficient migration and draining of dense residual melts through the anorthositic crystal mush could have taken place along sloping floors (zones of lesser permeability in the mush), which occur along the margins of the rising anorthositic diapirs. This process takes into account the restricted occurrence of the mafic intrusions in the margins of the massif anorthosites. In a later stage, when the anorthosite was nearly consolidated, the residual melts were more differentiated (evolved jotunites) and could have been extracted into extensional fractures in the cooling and contracting anorthositic body in a similar way as aplitic dikes are emplaced in granitic plutons. As in the Rogaland Anorthositic Province, these dikes are much more abundant than the small mafic intrusions, collection and transport along dikes was probably more efficient than draining through the crystal mush.     

Fluid inclusions in granulites, granulitized eclogites and garnet clinopyroxenites from the Dabie–Sulu terranes, eastern China

Minor granulites (believed to be pre-Triassic), surrounded by abundant amphibolite-facies orthogneiss, occur in the same region as the well-documented Triassic high- and ultrahigh-pressure (HP and UHP) eclogites in the Dabie–Sulu terranes, eastern China. Moreover, some eclogites and garnet clinopyroxenites have been metamorphosed at granulite- to amphibolite-facies conditions during exhumation. Granulitized HP eclogites/garnet clinopyroxenites at Huangweihe and Baizhangyan record estimated eclogite-facies metamorphic conditions of 775–805 °C and ≥15 kbar, followed by granulite- to amphibolite-facies overprint of ca. 750–800 °C and 6–11 kbar. The presence of (Na, Ca, Ba, Sr)-feldspars in garnet and omphacite corresponds to amphibolite-facies conditions. Metamorphic mineral assemblages and P–T estimates for felsic granulite at Huangtuling and mafic granulite at Huilanshan indicate peak conditions of 850 °C and 12 kbar for the granulite-facies metamorphism and 700 °C and 6 kbar for amphibolite-facies retrograde metamorphism. Cordierite–orthopyroxene and ferropargasite–plagioclase coronas and symplectites around garnet record a strong, rapid decompression, possibly contemporaneous with the uplift of neighbouring HP/UHP eclogites.

Carbonic fluid (CO₂-rich) inclusions are predominant in both HP granulites and granulitized HP/UHP eclogites/garnet clinopyroxenites. They have low densities, having been reset during decompression. Minor amounts of CH₄ and/or N₂ as well as carbonate are present. In the granulitized HP/UHP eclogites/garnet clinopyroxenites, early fluids are high-salinity brines with minor N₂, whereas low-salinity fluids formed during retrogression. Syn-granulite-facies carbonic fluid inclusions occur either in quartz rods in clinopyroxene (granulitized HP garnet clinopyxeronite) or in quartz blebs in garnet and quartz matrices (UHP eclogite). For HP granulites, a limited number of primary CO₂ and mixed H₂O–CO₂(liquid) inclusions have also been observed in undeformed quartz inclusions within garnet, orthopyroxene, and plagioclase which contain abundant, low-density CO₂±carbonate inclusions. It is suggested that the primary fluid in the HP granulites was high-density CO₂, mixed with a significant quantity of water. The water was consumed by retrograde metamorphic mineral reactions and may also have been responsible for metasomatic reactions (“giant myrmekites”) occurring at quartz–feldspar boundaries. Compared with the UHP eclogites in this region, the granulites were exhumed in the presence of massive, externally derived carbonic fluids and subsequently limited low-salinity aqueous fluids, probably derived from the surrounding gneisses.     

西藏定结高压基性麻粒岩(退变榴辉岩)的变质P-T轨迹及构造意义

定结（Dinggye）位于藏南高喜马拉雅结晶岩系的中部,研究该区域麻粒岩的变质P-T轨迹对于理解青藏高原的碰撞和抬升过程至关重要.通过对该地区的高压基性麻粒岩（退变榴辉岩）的岩相学观察,确定了4期矿物组合:（1）峰期榴辉岩相矿物组合（M₁）由石榴子石（核部）+绿辉石（假象）+石英+金红石组成;（2）高压麻粒岩相矿物组合（M₂）主要由石榴子石（幔部）+单斜辉石+斜长石+钛铁矿+角闪石+黑云母组成;（3）中压麻粒岩相矿物组合（M₃）由石榴子石（边缘）+斜方辉石+斜长石+钛铁矿+黑云母组成;（4）角闪岩相矿物组合（M₄）主要由角闪石+斜长石组成.在NCFMASHTO体系下,用THERMOCALC软件对该高压基性麻粒岩进行了热力学模拟.结合传统温压计和平均温压计计算结果,求得M₂、M₃、M₄阶段的温压条件分别为786~826 ℃、0.78~0.96 GPa;798~850 ℃、0.71~0.75 GPa;610~666 ℃、0.51~0.60 GPa,这指示了一条以峰期后近等温降压（ITD）为特征的顺时针P-T轨迹.结合已有地质资料,表明定结高压基性麻粒岩（退变榴辉岩）是喜马拉雅碰撞造山的产物,峰期后经历了近等温降压的构造抬升过程.      

Layered amphibolite sequence in NE Sardinia,Italy: remnant of a pre-Variscan mafic silicic layered intrusion?

A banded amphibolite sequence of alternating ultramafic, mafic (amphibolite) and silicic layers, tectonically enclosed within Variscan migmatites, outcrops at Monte Plebi (NE Sardinia) and shows similarities with leptyno-amphibolite complexes. The ultramafic layers consist of amphibole (75–98%), garnet (0–20%), opaque minerals (1–5%) and biotite (0–3%). The mafic rocks are made up of amphibole (65–80%), plagioclase (15–30%), quartz (0–15%), opaque minerals (2–3%) and biotite (0–2%). The silicic layers consist of plagioclase (60–75%), amphibole (15–30%) and quartz (10–15%). Alteration, metasomatic, metamorphic and hydrothermal processes did not significantly modify the original protolith chemistry, as proved by a lack of K₂O-enrichment, Rb-enrichment, CaO-depletion, MgO-depletion and by no shift in the rare earth element (REE) patterns. Field, geochemical and isotopic data suggest that ultramafic, mafic and silicic layers represent repeated sequences of cumulates, basic and acidic rocks similar to macrorhythmic units of mafic silicic layered intrusions. The ultramafic layers recall the evolved cumulates of Skaergaard and Pleasant Bay mafic silicic layered intrusions. Mafic layers resemble Thingmuli tholeiites and chilled Pleasant Bay mafic rocks. Silicic layers with Na₂O: 4–6 wt%, SiO₂: 67–71 wt% were likely oligoclase-rich adcumulates common in many mafic silicic layered intrusions. Some amphibolite showing a strong Ti-, P-depletion and REE-depletion are interpreted as early cumulates nearly devoid of ilmenite and phosphates. All Monte Plebi rocks have extremely low Nb, Ta, Zr, Hf content and high LILE/HFSE ratios, a feature inherited from the original mantle sources. The mafic and ultramafic layers show slight and strong LREE enrichment respectively. Most mafic layer samples plot in the field of continental tholeiites in the TiO₂–K₂O–P₂O₅ diagram and are completely different from N-MORB, E-MORB and T-MORB as regards REE patterns and Nd, Sr isotope ratios but show analogies with Siberian, Deccan and proto-Atlantic rift tholeiites. Comparisons with Thingmuli, Skaergaard and Kiglapait rocks and with experimental data suggest that the Monte Plebi intrusion was an open-to-oxygen system with fO₂ FMQ. Mafic and ultramafic samples yielded _Nd(460)=+0.79 /+3.06 and ⁸⁷Sr/⁸⁶Sr=0.702934–0.703426, and four silicic samples _Nd(460)=–0.53/–1.13; ⁸⁷Sr/⁸⁶Sr=0.703239–0.703653. Significant differences in Nd isotope ratios between mafic and silicic rocks prove that both groups evolved separately in deeper magma chambers, from different mantle sources, with negligible interaction with crustal material, and were later repeatedly injected within a shallower magma chamber. The spectrum of Sr and Nd isotope data is consistent with a slightly enriched mantle metasomatized during an event earlier than 460 Ma. The metasomatising component was represented by alkali-Th-rich fluids of crustal origin rather than by sedimentary materials, able to modify alkali and Sr–Nd isotope systematics. Monte Plebi layered amphibolites might represent the first example of a strongly metamorphosed fragment of an early Paleozoic mafic silicic layered intrusion emplaced in a thinning continental crust and then tectonically dismembered by Variscan orogeny.     

东昆仑夏日哈木铜镍矿镁铁质超镁铁质岩体岩相学、锆石U-Pb年代学、地球化学及其构造意义

文章报道了东昆仑夏日哈木铜镍矿成矿岩体的岩相学、锆石U-Pb年代学、全岩地球化学以及锆石Hf同位素资料,以确定该岩体的形成时代、岩石成因及其形成的构造环境。夏日哈木Ⅰ号镁铁质超镁铁质岩体位于昆中基底隆起花岗岩带中段,北侧靠近昆北断裂。岩体走向NEE,剖面呈平缓的“岩盆状”,地表出露面积约0.7 km2。该杂岩体主要由辉长苏长岩、斜方辉石岩、橄榄辉石岩、斜长二辉橄榄岩和方辉橄榄岩组成,橄榄岩相和辉石岩相是主要的Cu、Ni赋矿岩相。镁铁质超镁铁质岩体主量元素具有低硅(w(SiO₂)=36.68%~52.58%)、低钛(w(TiO2)=0.13%~0.47%)、高镁(w(MgO)=10.91%~35.81%)、贫碱(w(K₂O+Na₂O)=0.26%~1.95%)的特征,属亚碱性系列岩石,m/f为3.88~6.29,属铁质超基性岩类(m/f=2~6.5)。岩石稀土元素球粒陨石标准化配分模式为轻稀土富集型,(La/Yb)N=1.44~2.98,Eu异常不明显,相似的稀土元素配分模式说明岩体的同源性。岩石富集大离子亲石元素(Rb、Th、U、K),相对亏损高场强元素(Nb、Ta)。岩体中存在新元古代花岗岩的捕虏体以及La/Yb、Ce/Yb、Th/Yb、Nb/La、La/Sm比值显示岩体经历了有限的地壳混染。辉长苏长岩锆石的LA-MC ICPMS、U-Pb年代学研究表明,岩体形成年龄为(423±1) Ma,MSWD=0.14,属晚志留世。锆石的176Hf/177Hf比值为0.282 628~0.282 833,相应的εHf(t)均为正值(4.0~10.9),Lu-Hf的单阶段模式年龄(tDM1)为610~875 Ma,平均值为788 Ma,大于锆石U-Pb年龄。研究认为,岩体的岩浆源区主要为亏损地幔,可能有早期流体交代的富集岩石圈地幔组分的加入和地壳物质的混染。结合区域构造演化,文章认为岩体形成于碰撞后伸展的构造环境,可能与俯冲板片的断离作用有关。岩浆演化过程中橄榄石和斜方辉石的分离结晶作用和地壳中硫的加入可能是促使岩浆体系达到硫饱和的主要机制。     

Imaging downward granitic magma transport in the Rogaland Igneous Complex, SW Norway

Combining geological mapping and petrological, structural and geophysical (gravity and seismic) data already available for the late Proterozoic Rogaland Igneous Complex of Norway allows the 3D shape of the Bjerkreim–Sokndal layered intrusion to be modelled as a thick cumulate series capped by massive granitic rocks. Using the latter data, along with the spectacular convergent linear flow pattern that covers both the cumulates and the felsic rocks of this chamber, evidence is presented to show that the granitic material was down-dragged through the sinking of its high-density mafic floor into lower density anorthosites and granulitic gneisses. This example illustrates that downward gravity-driven flows of rocks were active, in addition to upward flows, in the building of the early crust up to late-Proterozoic times, helping to explain the geochemical and structural complexities of the old crust.     

Experimental study of liquid evolution in an Fe-rich,layered mafic intrusion: constraints of Fe-Ti oxide precipitation on the T-fO 2 and T-ϱ paths of tholeiitic magmas

The Newark Island layered intrusion, a composite intrusion displaying a similar fractionation sequence to the Skaergaard, has both dikes which preserved liquids fed into the intrusion and chilled pillows of liquids resident in the chamber. This study reports experimentally determined one atmosphere liquid lines of descent of these compositions as a function of oxygen fugacity which varies from QFM (quartz-fayalite-magnetite) to 0.5 log₁₀ units above IW (iron-wustite). These experiments reveal a strong oxygen fugacity dependence on the order of appearance and relative abundances of the Fe–Ti oxide minerals. Titanomagnetite saturates prior to ilmenite at QFM, but the order is reversed at lower oxygen fugacities. In the layered series of the Newark Island intrusion, ilmenite arrives shortly before titanomagnetite and the titanomagnetite/ilmenite ratio decreases monotonically after the cumulus appearance of titanomagnetite. Comparison of the crystallization sequence in the intrusion with that of the experiments requires that the oxygen fugacity in the intrusion increased relative to QFM before titanomagnetite saturation and decreased afterward, but always remained between the QFM and IW buffers. Similar trends in the modes of the Fe–Ti oxides (ilmenite and titanomagnetite) in the Skaergaard, Kiglapait, and Somerset Dam intrusions along with Fe₂O₃/FeO ratios in MORBs suggest that such a temperature-oxygen fugacity path may be typical of tholeiitic magma differentiation. Calculations of the temperature-density paths of the experimental liquids indicate that, at all possible oxygen fugacities, the density must have decreased abruptly after Fe–Ti oxide saturation. Accordingly, liquids replenishing the intrusion after Fe–Ti oxide saturation should pond at the bottom of the chamber, quenching against older cumulates. Field observation at the Newark Island intrusion confirm this prediction. The similarities in the fractionation paths of several other layered intrusions to that of the Newark Island intrusion suggest that the density of the liquids in these intrusions also decreased after Fe–Ti oxide saturation. Experiments on a suggested initial Skaergaard liquid are consistent with this model.     

Compositional classification of “kimberlitic” and “non-kimberlitic” ilmenite

Ilmenite is one of the common kimberlitic indicator minerals recovered during diamond exploration, and its distinction from non-kimberlitic rock types is important. This is particularly true for regions where these minerals are present in relatively low abundance, and they are the dominant kimberlitic indicator mineral recovered. Difficulty in visually differentiating kimberlitic from non-kimberlitic ilmenite in exploration concentrates is also an issue, and distinguishing kimberlitic ilmenite from those derive from other similar rocks, such as ultramafic lamprophyres, is practically impossible. Ilmenite is also the indicator mineral whose compositional variety has the most potential to resolve provenance issues related to mineral dispersions with contributions from multiple kimberlite sources.

Various published data sets from selected kimberlitic (including kimberlites, lamproites, and various ultramafic lamprophyres) and non-kimberlitic rock types have been compiled and evaluated in terms of their major element compositions. Compositional fields and bounding reference lines for ilmenites derived from kimberlites (sensu stricto), ultramafic lamprophyres, and other non-kimberlitic rock types have been defined primarily on MgO–TiO₂ graphs as well as MgO–Cr₂O₃ relationships.     

Carbonatite melt–CO2 fluid inclusions in mantle xenoliths from Tenerife, Canary Islands: a story of trapping, immiscibility and fluid–rock interaction in the upper mantle

Three types of fluid inclusions have been identified in olivine porphyroclasts in the spinel harzburgite and lherzolite xenoliths from Tenerife: pure CO₂ (Type A); carbonate-rich CO₂–SO₂ mixtures (Type B); and polyphase inclusions dominated by silicate glass±fluid±sp±silicate±sulfide±carbonate (Type C). Type A inclusions commonly exhibit a “coating” (a few microns thick) consisting of an aggregate of a platy, hydrous Mg–Fe–Si phase, most likely talc, together with very small amounts of halite, dolomite and other phases. Larger crystals (e.g. (Na,K)Cl, dolomite, spinel, sulfide and phlogopite) may be found on either side of the “coating”, towards the wall of the host mineral or towards the inclusion center. These different fluids were formed through the immiscible separations and fluid–wall-rock reactions from a common, volatile-rich, siliceous, alkaline carbonatite melt infiltrating the upper mantle beneath the Tenerife. First, the original siliceous carbonatite melt is separated from a mixed CO₂–H₂O–NaCl fluid and a silicate/silicocarbonatite melt (preserved in Type A inclusions). The reaction of the carbonaceous silicate melt with the wall-rock minerals gave rise to large poikilitic orthopyroxene and clinopyroxene grains, and smaller neoblasts. During the metasomatic processes, the consumption of the silicate part of the melt produced carbonate-enriched Type B CO₂–SO₂ fluids which were trapped in exsolved orthopyroxene porphyroclasts. At the later stages, the interstitial silicate/silicocarbonatite fluids were trapped as Type C inclusions. At a temperature above 650 °C, the mixed CO₂–H₂O–NaCl fluid inside the Type A inclusions were separated into CO₂-rich fluid and H₂O–NaCl brine. At T<650 °C, the residual silicate melt reacted with the host olivine, forming a reaction rim or “coating” along the inclusion walls consisting of talc (or possibly serpentine) together with minute crystals of NaCl, KCl, carbonates and sulfides, leaving a residual CO₂ fluid. The homogenization temperatures of +2 to +25 °C obtained from the Type A CO₂ inclusions reflect the densities of the residual CO₂ after its reactions with the olivine host, and are unrelated to the initial fluid density or the external pressure at the time of trapping. The latter are restricted by the estimated crystallization temperatures of 1000–1200 °C, and the spinel lherzolite phase assemblage of the xenolith, which is 0.7–1.7 GPa.