Water-deficient Calc-alkaline Plutonic Rocks of Northeastern Superior Province, Canada: Significance of Charnockitic Magmatism

Calc-alkaline batholiths of the Archaean Minto block, northeasternSuperior Province, Canada, have pyroxene- and hornblende-bearingmineral assemblages inferred to have crystallized from hot,water-undersaturated magmas at 2·729–2·724Ga. A regional amphibolite- to granulite-facies tectonothermalevent at 2·70 Ga resulted in mild to negligible metamorphiceffects on the dominantly granodioritic units. Geochemical,textural and thermobarometric studies define the crystallizationhistory in compositions ranging from cumulate pyroxenite throughquartz diorite, granodiorite, granite, and syn-magmatic gabbroicdykes. Early magmatic assemblages include orthopyroxene, clinopyroxene,plagioclase, biotite, Fe–Ti oxides and ternary feldspar,indicating crystallization from magmas containing <2 wt %H₂O at 1100–900°C. Water enrichment in the residualmelt induced hornblende crystallization at 5 ± 1 kbar,800–600°C. Characterized by a continuum of large ionlithophile element (LILE)-enriched, high field strength element(HFSE)-depleted compositions, the I-type suite resembles moderncontinental arc batholiths in composition and size but not primarymineralogy. Magmatic arcs produced between 2·75 and 1·85Ga commonly have charnockitic components, possibly because slab-derivedfluids interacted with mantle wedges at ambient temperatureshigher by 100°C than at present, producing large volumesof water-deficient magma. KEY WORDS: granitoid rocks; igneous pyroxenes; water-undersaturated magma; charnockite     

Petrogenesis of a Late Jurassic Peraluminous Volcanic Complex and its High-Mg, Potassic, Quenched Enclaves at Xiangshan, Southeast China

A late Mesozoic belt of volcanic–intrusive complexes occursin SE China. Volcanic activity at Xiangshan in the NW of thebelt took place mainly in the Late Jurassic (158–135 Ma).The volcanic rocks from the Xiangshan volcanic complex includerhyolitic crystal tuffs, welded tuffs, rhyolite lavas, porphyriticlavas, and associated subvolcanic rocks. Mineral assemblagesin these magmatic rocks include K-feldspar, plagioclase, quartz,Fe-rich biotite and minor amphibole, orthopyroxene and almandine.Mineral geothermometry indicates a high crystallization temperature(>850°C) for the Xiangshan magmas. The volcanic rocksare generally peraluminous; SiO₂ contents are between 65·4%and 76·8% and the samples have high alkalis, rare earthelements (REE), high field strength elements and Ga contentsand high Ga/Al ratios, but are depleted in Ba, Sr and transitionmetals. Trace element geochemistry and Sr–Nd–O isotopesystematics imply that the Xiangshan magmas were probably derivedfrom partial melting of Middle Proterozoic metamorphic lower-crustalrocks that had been dehydrated during an earlier thermal event.These features suggest an A-type affinity. Quenched mafic enclaves,hosted by the subvolcanic rocks, consist mainly of alkali feldspar,plagioclase, clinopyroxene, phlogopite and amphibole. Geothermometrycalculations indicate that the primary magmas that chilled toform the quenched enclaves had anomalously high temperatures(>1200°C). The quenched enclaves have boninitic affinities;for example, intermediate SiO₂ contents, high MgO and low TiO₂contents, high Mg-numbers and high concentrations of Sc, Ni,Co and V. However, they also have shoshonitic characteristics,e.g. enrichment in alkalis, high K₂O contents with high K₂O/Na₂Oratios, high light REE and large ion lithophile element contents,low initial _Nd values (–4·2) and high initial ⁸⁷Sr/⁸⁶Srratios (0·7081). We suggest a phlogopite-bearing spinelharzburgitic lithospheric mantle source for these high-Mg potassicmagmas. Underplating of such anomalously high-temperature magmascould have induced granulite-facies lower-crustal rocks to partiallymelt and generate the Xiangshan A-type volcanic suite. A back-arcextensional setting, related to subduction of the Palaeo-Pacificplate, is favoured to explain the petrogenesis of the Xiangshanvolcanic complex and quenched enclaves. KEY WORDS: volcanic complex; quenched enclaves; petrology; geochemistry; back-arc extension setting; Xiangshan; SE China     

Archaean to Proterozoic Crustal Evolution in the Central Zone of the Limpopo Belt (South Africa-Botswana): Constraints from Combined U-Pb and Lu-Hf Isotope Analyses of Zircon

A combined set of U–Pb and Lu–Hf in situ laser ablationICP-(MC)-MS zircon analyses were obtained from orthogneissesand granitoids in the Central Zone of the Limpopo Belt, whichcomprises the Beit Bridge and Mahalapye complexes. The resultsindicate that by combining the two isotope systems primary magmaticzircon domains can be distinguished from those formed duringlater metamorphic events, even if the distinct zircon domainsunderwent multiple Pb loss and the texture–age relationships,as obtained by cathodoluminescence images and U–Pb analyses,are ambiguous. Furthermore, the applied technique allows distinctionof zircon grains formed in juvenile magmas from those generatedby melting of older continental crust or affected by substantialcrustal contamination. The combined U–Pb and Lu–Hfdata reveal that the Sand River gneiss suite of the Beit BridgeComplex was emplaced at 3283 ± 8 Ma and formed from meltingof an older Archaean crust, which was derived from a depletedmantle source at around 3·65 Ga. The hafnium model age(T_DM^Hf) is significantly older than those obtained from zirconsfrom numerous Neoarchaean granitoids of the Beit Bridge Complex,comprising the Singelele gneiss (2647 ± 12 Ma), the Bulaigranite (2612 ± 7 Ma), the Regina gneiss (2649 ±9 Ma) and two samples of the Zanzibar gneiss (2613 ±6 Ma). These granitoids show initial Hf(t) values between +0·5 and –7·1, which correspond to initialT_DM^Hf between 3·46 and 3·01 Ga. These variableT_DM^Hf_initial and Hf(t)_initial values are interpreted to be theresult of different mixtures of reworked 3·65 Ga Palaeoarchaeancrust with juvenile magmas extracted from the depleted mantleduring the Neoarchaean at 2·65 Ga. This conclusion issupported by results obtained from the Mahalapye Complex, whichwas affected by migmatization and granite intrusions duringthe Palaeoproterozoic at 2·02–2·06 Ga. TheMokgware granite (2019 ± 9 Ma) contains zircon xenocrystswith Pb–Pb ages of 2·52–2·65 Ga and2·93 Ga and hafnium model ages of 3·0–3·4Ga, indicating that this granite is derived from remelting ofArchaean crust. In contrast, uniform T_DM^Hf_initial ages of 2·61–2·67Ga obtained from a diorite gneiss (2061 ± 6 Ma) of theMahalapye Complex indicate that its protolith may have beenformed from remelting of a Neoarchaean juvenile crust. VariableHf(t)_initial values from –3·7 to +6·3 ofzircon cores (2711 ± 11 Ma) in an adjacent leucosomealso support a model of mixing of juvenile mantle derived matterwith older crust in the Neoarchaean. KEY WORDS: Archaean; Palaeoproterozoic; Limpopo Belt; zircon, U–Pb dating; Lu–Hf isotopes; LA-ICP-MS     

Lithospheric Origin of Oligocene-Miocene Magmatism in Central Chile: U-Pb Ages and Sr-Pb-Hf Isotope Composition of Minerals

Establishing the petrogenesis of volcanic and plutonic rocksis a key issue in unraveling the evolution of distinct subduction-relatedtectonic phases occurring along the South American margin. Thisis particularly true for Cenozoic times when large volumes ofmagma were produced in the Andean belt. In this study we havefocused on Oligo-Miocene magmatism in central Chile at 33°S.Our data include field and petrographic observations, whole-rockmajor and trace element analyses, U–Pb zircon dating,and Pb, Sr, and Hf isotope analyses of plagioclase, clinopyroxene,and zircon mineral separates. Combined with earlier dating resultsthe new zircon ages define a 28·8–5·2 Maperiod of plutonic and volcanic activity that ceased as a consequenceof flattening subduction of the Nazca–Farallon plate.Rare earth elements patterns are variable, with up to 92 timeschondrite concentrations for light rare earth elements yielding(La/Yb)_N between 3·6 and 7·0, and an absence ofEu anomalies. Initial Pb isotope signatures are in the rangeof 18·358–19·023 for ²⁰⁶Pb/ ²⁰⁴Pb, 15·567–15·700for ²⁰⁷Pb/ ²⁰⁴Pb and 38·249–39·084 for ²⁰⁸Pb/²⁰⁴Pb. Initial ⁸⁷Sr/ ⁸⁶Sr are mostly in the range of 0·70369–0·70505,with two more radiogenic values at 0·7066. Initial Hfisotopic compositions of zircons yield exclusively positiveHf_i ranging between + 6·9 and + 9·6. The newlydetermined initial isotope characteristics of the Oligo-Miocenemagmas suggest that the mantle source lithologies are differentfrom both those of Pacific mid-ocean ridge basalt and oceanisland basalt, plotting in the field of reference values forsubcontinental lithospheric mantle, characterized by moderatelarge ion lithophile element–high field strengh elementdepletion and high ²³⁸U/ ²⁰⁴Pb. A Hf model age of 2 Ga is estimatedfor the formation of the subcontinental mantle–continentalcrust assemblage in the region, suggesting that the initialSr and Pb isotope ratios inferred for the source of the Oligo-Mioceneparental magmas are the result of later Rb and U enrichmentcaused by mantle metasomatism. A time-integrated model Rb/Srof 0·039 and µ 16 are estimated for the sourceof the parental magmas, consistent with ratios measured in peridotitexenoliths from continental areas. Evolution from predominant(>90%) basaltic–gabbroic to andesitic–dioriticmagmas seems to involve a combination of (1) original traceelement differences in the metasomatized subcontinental mantle,(2) different degrees of partial melting and (3) fractionalcrystallization in the garnet- and spinel-peridotite stabilityfields. The genesis of more differentiated magmas reaching rhyolitic–graniticcompositions most probably also includes additional crystalfractionation at both shallow mantle depths and within the crust,possibly leading to some very minor assimilation of crustalmaterial. KEY WORDS: calc-alkaline magmatism; Oligo-Miocene; U–Pb dating; Sr–Pb–Hf isotopes; central Chile     

Geochemistry of South African On- and Off-craton, Group I and Group II Kimberlites: Petrogenesis and Source Region Evolution

Bulk-rock geochemical compositions of hypabyssal kimberlites,emplaced through the Archaean Kaapvaal craton and ProterozoicNamaqua–Natal belt, are used to estimate close-to-primarymagma compositions of Group I kimberlites (Mg-number = 0·82–0·87;22–28 wt % MgO; 21–30 wt % SiO₂; 10–17 wt% CaO; 0·2–1·7 wt % K₂O) and Group II kimberlites(Mg-number = 0·86–0·89; 23–29 wt %MgO; 28–36 wt % SiO₂; 8–13 wt % CaO; 1·6–4·6wt % K₂O). Group I kimberlites are distinguished from GroupII by their lower Ba/Nb (<12), Th/Nb (<1·1) andLa/Nb (<1·1) but higher Ce/Pb (>22) ratios. Thedistinct rare earth element patterns of the two types of kimberlitesindicate a more highly metasomatized source for Group II kimberlites,with more residual clinopyroxene and less residual garnet. Thesimilarity of Sr and Nd isotope ratios and diagnostic traceelement ratios (Ce/Pb, Nb/U, La/Nb, Ba/Nb, Th/Nb) of Group Ikimberlites to ocean island basalts (OIB), but more refractoryMg-numbers and Ni contents, are consistent with derivation ofGroup I kimberlites from subcontinental lithospheric mantle(SCLM) that has been enriched by OIB-like melts or fluids. Sourceenrichment ages and plate reconstructions support a direct associationof these melts or fluids with Mesozoic upwelling beneath southernAfrica of a mantle plume(s), at present located beneath thesouthern South Atlantic Ocean. In contrast, the geochemicalcharacteristics of both on- and off-craton Group II kimberlitesshow strong similarity to calc-alkaline magmas, particularlyin their Nb and Ta depletion and Pb enrichment. It is suggestedthat Group II kimberlites are derived from both Archaean andProterozoic lithospheric mantle source regions metasomatizedby melts or fluids associated with ancient subduction events,unrelated to mantle plume upwelling. The upwelling of mantleplumes beneath southern Africa during the Mesozoic, at the timeof Gondwana break-up, may have acted as a heat source for partialmelting of the SCLM and the generation of both Group I and GroupII kimberlite magmas. KEY WORDS: kimberlite; geochemistry; petrogenesis; mantle plumes; South Africa     

Subduction Influence on Oxygen Fugacity and Trace and Volatile Elements in Basalts Across the Cascade Volcanic Arc

Fluids or melts derived from a subducting plate are often citedas a mechanism for the oxidation of arc magmas. What remainsunclear is the link between the fluid, oxygen fugacity, andother major and trace components, as well as the spatial distributionof the impact of those fluids. To test the potential effectsof addition of a subduction-derived fluid or melt to the sub-arcmantle, olivine-hosted melt inclusions from primitive basalticlavas sampled from across the central Oregon Cascades (43°–45°N)have been analyzed for major, trace and volatile elements andfO₂. Oxygen fugacity was determined in melt inclusions fromsulfur speciation determined by electron microprobe and fromolivine–chromite oxygen geobarometry. The overall rangein fO₂ based on sulfur speciation measurements is from <–0·25log units to + 1·9 log units (FMQ, where FMQ is fayalite–magnetite–quartzbuffer). Oxygen fugacity is positively correlated with fluid-mobiletrace element and light rare earth element contents in basaltsgenerated by relatively low-degree partial melting. Establishinga further correlation between fO₂ and fluid-mobile trace elementabundances with position along the arc requires the basaltsto be subdivided into shoshonitic, calc-alkaline, low-K tholeiiteand enriched intraplate basalt groups. Melt inclusions fromenriched intraplate and shoshonitic lavas show increasing fO₂and trace element abundances closer to the trench, whereas calc-alkalinemelt inclusions exhibit no significant across-arc variations.Low-K tholeiitic melt inclusions record an increase in incompatibletrace elements closer to the trench; however, there is no correlatedincrease in fO₂. The correlation observed in enriched intraplateand shoshonitic melt inclusions is interpreted to reflect aprogressively greater proportion of a fluid-rich, oxidized subductioncomponent in magmas generated nearer the subduction zone. Significantly,calc-alkaline melt inclusions with high ratios of large ionlithophile elements to high field strength elements, characteristicof ‘typical’ arc magmas, have oxidation states indistinguishablefrom low-K tholeiite and enriched intraplate basalt melt inclusions.The lack of across-arc geochemical variation in calc-alkalinemelt inclusions may suggest that these basalts are not necessarilythe most appropriate magmas for examining recent addition ofa subduction component to the sub-arc mantle. Flux and batchmelt model results produce a wide range of predicted amountsof melting and subduction component added to the mantle source;however, general trends characterized by increased melting andproportion of the subduction component from enriched intraplate,to low-K tholeiite, to calc-alkaline are robust. The model resultsdo not require enriched intraplate, low-K tholeiite and calc-alkalinemagmas to be produced from the same more fertile mantle source.However, enriched intraplate magmas, in contrast to calc-alkalineand low-K tholeiite magmas, cannot be generated from a depletedmantle source. Flux or batch melting of either the more fertileor depleted mantle sources used to generate the low-K tholeiite,calc-alkaline, and enriched intraplate magmas cannot reproduceshoshonitic compositions, which require a significantly depletedmantle source strongly metasomatized by a subduction component.The potential mantle source for shoshonitic basalts has a predictedfO₂ (after oxidation) from + 0·3 to + 2·4 logunits (FMQ) whereas the mantle source for low-K tholeiite, calc-alkaline,and enriched intraplate magmas may range from –1·1to + 0·7 log units (FMQ). KEY WORDS: basalt; Cascades; melt inclusions; oxidation state; volatiles     

Petrogenesis of an Alkali Syenite-Granite-Rhyolite Suite in the Yanshan Fold and Thrust Belt, Eastern North China Craton: Geochronological, Geochemical and Nd-Sr-Hf Isotopic Evidence for Lithospheric Thinning

The Yanshan Fold and Thrust Belt in eastern China has been intrudedby a series of alkalic igneous rocks, ranging in compositionfrom granite and rhyolite to syenite and trachyte. Laser ablationinductively coupled plasma mass spectrometry U–Pb analysesof zircon from three alkaline suites yield Early Cretaceousages of 130–117 Ma. Three groups of rocks have been identifiedbased on their mineralogical, geochemical and Sr–Nd–Hfisotope characteristics. The alkali granites and rhyolites areferroan and have low Al₂O₃, MgO, CaO, Sr, Ba and Eu concentrationsand high SiO₂, total Fe₂O₃, K₂O, Nb, Ga, Ta, Th and heavy rareearth element abundances and Ga/Al ratios. Geochemical dataand Sr-, Nd- and zircon Hf-isotopic compositions [(⁸⁷Sr/⁸⁶Sr)_i= 0·7050–0·7164, _Nd(t) = –8·4to –13·6 and _Hf(t) = –5·7 to –16·8]indicate that they were probably generated by shallow dehydrationmelting of biotite- or hornblende-bearing granitoid crustalsource rocks and then mixed with contemporaneous magma froma mantle and/or lower crustal source. Ferroan syenites havedistinct geochemical features from those of the alkaline granitesand rhyolites, suggesting that they were produced by clinopyroxeneand plagioclase fractionation of melt derived from an enrichedmantle source, mixed with lower and upper crustal-derived magmas.The magnesian syenites and trachytes have Sr-, Nd- and zirconHf-isotopic compositions that are distinct from those of theferroan syenites. They were mainly derived from partial meltingof lower crustal materials, mixed with enriched mantle-derivedalkali basaltic magma. The emplacement of an alkali syenite–granite–rhyolitesuite, coeval with the formation of metamorphic core complexesand pull-apart basins in eastern China, indicates they formedin an extensional setting, possibly as a result of lithosphericthinning. KEY WORDS: alkaline rocks; zircon U–Pb dating; petrogenesis; crustal extension; Yanshan Fold and Thrust Belt; North China Craton     

Transformation of Archaean Lithospheric Mantle by Refertilization: Evidence from Exposed Peridotites in the Western Gneiss Region, Norway

Orogenic peridotites occur enclosed in Proterozoic gneissesat several localities in the Western Gneiss Region (WGR) ofwestern Norway; garnet peridotites typically occur as discretezones within larger bodies of garnet-free, chromite-bearingdunite and are commonly closely associated with pyroxenitesand eclogites. The dunites of the large Almklovdalen peridotitebody have extremely depleted compositions (Mg-number 92–93·6);the garnet peridotites have lower Mg-number (90·6–91·7)and higher whole-rock Ca and Al contents. Post-depletion metasomatismof both rock types is indicated by variable enrichment in thelight rare earth elements, Th, Ba and Sr. The dunites can bemodelled as residues after very high degrees (>60%) of meltextraction at high pressure (5–7 GPa), inconsistent withthe preservation of lower degrees of melting in the garnet peridotites.The garnet peridotites are, therefore, interpreted as zonesof melt percolation, which resulted in refertilization of thedunites by a silicate melt rich in Fe, Ca, Al and Na, but notTi. Previous Re–Os dating gives Archaean model ages forthe dunites, but mixed Archaean and Proterozoic ages for thegarnet peridotites, suggesting that refertilization occurredin Proterozoic time. At least some Proterozoic lithosphere mayrepresent reworked and transformed Archaean lithospheric mantle. KEY WORDS: Archaean mantle; Proterozoic mantle; Western Gneiss Region, Norway; mantle metasomatism; garnet peridotite     

Synplutonic mafic dykes from late Archaean granitoids in the Eastern Dharwar Craton,southern India

We present a first overview of the synplutonic mafic dykes (mafic injections) from the 2.56–2.52 Ga calcalkaline to potassic plutons in the Eastern Dharwar Craton (EDC). The host plutons comprise voluminous intrusive facies (dark grey clinopyroxene-amphibole rich monzodiorite and quartz monzonite, pinkish grey porphyritic monzogranite and grey granodiorite) located in the central part of individual pluton, whilst subordinate anatectic facies (light grey and pink granite) confined to the periphery. The enclaves found in the plutons include highly angular screens of xenoliths of the basement, rounded to pillowed mafic magmatic enclaves (MME) and most spectacular synplutonic mafic dykes. The similar textures of MME and adjoining synplutonic mafic dykes together with their spatial association and occasional transition of MME to dismembered synplutonic mafic dykes imply a genetic link between them. The synplutonic dykes occur in varying dimension ranging from a few centimeter width upto 200 meters width and are generally dismembered or disrupted and rarely continuous. Necking of dyke along its length and back veining of more leucocratic variant of the host is common feature. They show lobate as well as sharp contacts with chilled margins suggesting their injection during different stages of crystallization of host plutons in magma chamber. Local interaction, mixing and mingling processes are documented in all the studied crustal corridors in the EDC. The observed mixing, mingling, partial hybridization, MME and emplacement of synplutonic mafic dykes can be explained by four stage processes: (1) Mafic magma injected during very early stage of crystallization of host felsic magma, mixing of mafic and felsic host magma results in hybridization with occasional MME; (2) Mafic magma introduced slightly later, the viscosities of two magmas may be different and permit only mingling where by each component retain their identity; (3) When mafic magma injected into crystallizing granitic host magma with significant crystal content, the mafic magma is channeled into early fractures and form dismembered synplutonic mafic dykes and (4) Mafic injections enter into largely crystallized (>80% crystals) granitic host results in continuous dykes with sharp contacts. The origin of mafic magmas may be related to development of fractures to mantle depth during crystallization of host magmas which results in the decompression melting of mantle source. The resultant hot mafic melts with low viscosity rise rapidly into the crystallizing host magma chamber where they interact depending upon the crystallinity and viscosity of the host. These hot mafic injections locally cause reversal of crystallization of the felsic host and induce melting and resultant melts in turn penetrate the crystallizing mafic body as back veining. Field chronology indicates injection of mafic magmas is synchronous with emplacement of anatectic melts and slightly predates the 2.5 Ga metamorphic event which affected the whole Archaean crust. The injection of mafic magmas into the crystallizing host plutons forms the terminal Archaean magmatic event and spatially associated with reworking and cratonization of Archaean crust in the EDC.     

A Metamorphosed, Early Archaean Chromitite from West Greenland: Implications for the Genesis of Archaean Anorthositic Chromitites

An early Archaean (>3·81 Ga) chromitite–ultramaficlayered body from the Ujaragssuit nunât area, west Greenland,may represent the Earth’s oldest chromitite. The layeredbody occurs as a large xenolith (800 m x 100 m) entrained withintonalitic gneisses and preserves primary igneous layering andtextures. New Re–Os and Pb–Pb isotope results supportthe view that it has been metamorphosed twice, in the earlyand late Archaean at 3·75 Ga and 2·8 Ga. Mineralchemistry and textures indicate that the chromite compositionspreserve two different evolutionary trends. There is a mainmagmatic trend in which Cr/(Cr + Al) ratios remain relativelyconstant but in which there is strong enrichment in Fe³⁺, Fe²⁺and Ti with progressive differentiation. This trend is a compositeof magmatic-liquidus, magmatic-cooling and subsolidus re-equilibrationprocesses. A second trend is defined by chromites from harzburgitesin the upper part of the layered body. These chromites showmagmatic replacement textures in which Fe-rich chromites arealtered to aluminous chromites. Chromites showing magmatic replacementtextures are thought to have formed by reaction with a late,interstitial melt during the solidification of the layered body.The close association between the Fe³⁺–Cr-chromites ofthe main trend and Al-rich chromites of the type found in otherArchaean megacrystic anorthosites suggest a magmatic-geneticrelationship between the two types of chromite. We propose thatanorthositic chromites form in an Fe-rich basaltic melt derivedfrom a komatiitic, boninitic or basaltic parent magma throughreaction between the melt and early-formed Fe-rich chromite. KEY WORDS: chromite; anorthosite; Archaean; Greenland; Re–Os     

Evolution of Archaean Southern Indian lithospheric mantle: a geochemical study of Proterozoic Agali — Coimbatore dykes

 Agali–Coimbatore dolerite dykes constitute an important Proterozoic magmatic event that affected the south Indian shield. Rb-Sr whole rock isotope data yield an “errorchron” of 2369±400 Ma (2σ error) which is within error of the reported 2030±65 Ma K-Ar age. The dyke magmas were evolved Fe-rich tholeiitic melts produced by fractionation of clinopyroxene, orthopyroxene and olivine in the initial stages. Plagioclase became a fractionation phase during the latter stages of crystallization. The dykes characteristically have high ⁸⁷Sr/⁸⁶Sr_i (0.703–0.706) and are enriched in large-ion lithophile and light rare earth elements relative to primordial mantle values and show negative Nb anomalies. These compositional characteristics are interpreted as source mantle characteristics whereas some crustal effects are visible in some samples with high initial ⁸⁷Sr/⁸⁶Sr. Peridotite with minor hydrous metasomatic phases like amphibole (and phlogopite) within the shallow lithospheric mantle could be a potential source material for the dykes. However, at this stage we cannot convincingly differentiate whether the source of the parent magmas is solely lithospheric or a product of asthenosphere-lithosphere mixing. The δ¹⁸O values of the dykes range from +5.2 to +7.2 per mil (vs standard mean oceanic water). Initial Nd isotope values at the time of dyke intrusion (ɛ_Nd at t=2.0 Ga) range from −2.3 to −4.8. Whole rocks define a correlation on an Sm-Nd isochron plot with a slope equivalent to an age of 3.15±0.53 Ga (2σ error); Sm-Nd crustal residence ages average at 2.87 Ga. The isochron age does not appear to be the result of systematic mixing with an older crustal component. These results together with trace element geochemistry suggest that the south Indian mantle lithosphere developed by addition of enriched melts/fluids at about 3.0 Ga synchronously with major crustal gene- ration in the south Indian shield. Received 20 June 1994/Accepted: 17 May 1995     

Volcanism in the Vitim Volcanic Field, Siberia: Geochemical Evidence for a Mantle Plume Beneath the Baikal Rift Zone

The Baikal Rift is a zone of active lithospheric extension adjacentto the Siberian Craton. The 6–16 Myr old Vitim VolcanicField (VVF) lies approximately 200 km east of the rift axisand consists of 5000 km³ of melanephelinites, basanites, alkaliand tholeiitic basalts, and minor nephelinites. In the volcanicpile, 142 drill core samples were used to study temporal andspatial variations. Variations in major element abundances (e.g.MgO = 3·3–14·6 wt %) reflect polybaric fractionalcrystallization of olivine, clinopyroxene and plagioclase. ⁸⁷Sr/⁸⁶Sr_i(0·7039–0·7049), ¹⁴³Nd/¹⁴⁴Nd_i (0·5127–0·5129)and ¹⁷⁶Hf/¹⁷⁷Hf_i (0·2829–0·2830) ratiosare similar to those for ocean island basalts and suggest thatthe magmas have not assimilated significant amounts of continentalcrust. Variable degrees of partial melting appear to be responsiblefor differences in Na₂O, P₂O₅, K₂O and incompatible trace elementabundances in the most primitive (high-MgO) magmas. Fractionatedheavy rare earth element (HREE) ratios (e.g. [Gd/Lu]_n > 2·5)indicate that the parental magmas of the Vitim lavas were predominantlygenerated within the garnet stability field. Forward major elementand REE inversion models suggest that the tholeiitic and alkalibasalts were generated by decompression melting of a fertileperidotite source within the convecting mantle beneath Vitim.Ba/Sr ratios and negative K anomalies in normalized multi-elementplots suggest that phlogopite was a residual mantle phase duringthe genesis of the nephelinites and basanites. Relatively highlight REE (LREE) abundances in the silica-undersaturated meltsrequire a metasomatically enriched lithospheric mantle source.Results of forward major element modelling suggest that meltingof phlogopite-bearing pyroxenite veins could explain the majorelement composition of these melts. In support of this, pyroxenitexenoliths have been found in the VVF. High Cenozoic mantle potentialtemperatures (1450°C) predicted from geochemical modellingsuggest the presence of a mantle plume beneath the Baikal RiftZone. KEY WORDS: Baikal Rift; mafic magmatism; mantle plume; metasomatism; partial melting     

Geochemistry and petrogenesis of the Proterozoic dykes in Tamil nadu, southern India: another example of the Archaean lithospheric mantle source

Approximately 1650-Ma-old NW/SE and NE/SW-trending dolerite dykes in the Tiruvannamalai (TNM) area and approximately 1800-Ma-old NW/SE-trending dolerite dykes in the Dharmapuri (DP) area constitute major Proterozoic dyke swarms in the high-grade granulite region of Tamil nadu, southern India. The NW- and NE-trending TNM dykes are compositionally very similar and can be regarded as having been formed during a single magmatic episode. The DP dykes may relate to an earlier similar magmatic episode. The dolerites are Fe-rich tholeiites and most of the elemental variations can be explained in terms of fractional crystallisation. Clinopyroxene and olivine are the inferred ferromagnesian fractionation phases followed by plagioclase during the late fractionation stages. All the studied dykes have, similar to many continental flood basalts (CFB), large-ion lithophile element (LILE) and light rare-earth element (LREE) enrichment and Nb and Ta depletion. The incompatible element abundance patterns are comparable to the patterns of many other Proterozoic dykes in India and Antarctica, to the late Archaean (～2.72 Ga) Dominion volcanics in South Africa and to the early Proterozoic (～2.0 Ga) Scourie dykes of Scotland. The geochemical characteristics of the TNM and DP dykes cannot be explained by crustal contamination alone. Instead, they are consistent with derivation from an enriched lithospheric mantle source which appears to have been developed much earlier than the dyke intrusions during a major crustal building event in the Archaean. The dyke magmas may have been formed by dehydration melting induced by decompression and lithospheric attenuation or plume impingement at the base of the lithosphere. These magmas, compared with CFB, appear to be the minor partial melts from plume heads of smaller diameter and of shallow origin (650 km). Therefore, the Proterozoic thermal events could induce crustal attenuation and dyke intrusions in contrast to the extensive CFB volcanism and continental rifting generally associated with the Phanerozoic plumes of larger head diameter (>1000 km) and of deeper origin (at crust mantle boundary).     

Constraints on Archaean crustal evolution of the Zimbabwe craton: a U-Pb zircon,Sm-Nd and Pb-Pb whole-rock isotope study

 The U-Pb ages of zircons from seven felsic volcanic and plutonic rocks from northern Zimbabwe combined with field data and Pb-Pb and Sm-Nd whole-rock isotope data, constrain the timespan of development of the Harare-Shamva granite-greenstone terrain and establish the relative involvement of juvenile mantle-derived and reworked crustal material. Basement-cover field relationships and isotope and geochemical data demonstrate that the greenstones were deposited onto 3.2–2.8 Ga basement gneisses, in ensialic, continental basins. Geodynamic models for the generation of the areally extensive bimodal magmatic products and growth of the pre-existing crustal nucleus consistent with our interpretations are rift-related: (1) intracontinental rifting related to mantle plume activity or; (2) rifting in a back-arc environment related to a marginal volcanic arc. The data, in conjunction with field evidence, do not indicate the presence and accretion of an older (ca. 2.70 Ga) and a younger (ca. 2.65 Ga) greenstone sequence in the Harare part of the greenstone belt, as was recently postulated on the basis of SHRIMP zircon ages. Zircon ages for basal felsic volcanics (2715±15 Ma) and a subvolcanic porphyry (2672±12 Ma) constrain the initiation and termination of deposition of the greenstone sequence. The timespan of deposition of the Upper Bulawayan part of the greenstone sequence corresponds well with radiometric ages for Upper Bulawayan greenstones in the central and southern part of the craton and supports the concept of craton-wide lithostratigraphic correlations for the late Archaean in Zimbabwe. Zircon ages for a syn-tectonic gneiss (2667±4 Ma) and a late syn-tectonic intrusive granodiorite (2664±15 Ma) pinpoint the age of deformation of the greenstone sequence and compare well with a Pb-Pb age of shear zone related gold mineralization (2659±13 Ma) associated with the latter intrusive phase. The intimate timing relation of greenstone deformation and granitoid emplacement, but also the metamorphic evidence for a thermal effect of the batholiths on the surrounding greenstone belts, and the structural and strain patterns in the greenstone sequence around and adjacent to the batholiths, imply that the intrusion of the granitoids had a significant influence on the tectono-thermal evolution of the greenstone belt. Prolonged magmatic activity is indicated by the zircon ages of small, post-tectonic plutons intrusive into the greenstone belt, with a mineralized granodiorite dated at 2649±6 Ma and an unmineralized tonalite at 2618± 6 Ma. The 2601±14 Ma crystallization age of an “external” Chilimanzi-type granite agrees well with existing radiometric ages for similar granites within the southern part of the craton, demonstrating a craton-wide event and heralding cratonization. The similarity between U-Pb zircon ages and T_DM model ages (2.65–2.62 Ga) and the positive ɛNd_T values (+3 to +2) for the late syn-tectonic and post-tectonic intrusive plutons within the greenstone belt indicate magmatism was derived directly from the mantle or by anatexis of lower crustal sources, with very short crustal residence times, and minor contamination with older crust. The rather high model μ₁ values (8.2–8.6) are unlikely to indicate the involvement of significant amounts of older crust and may be inherited from a high U/Pb mantle source, as was suggested by previous workers for the Archaean mantle beneath Southern Africa. The older T_DM ages for the felsic volcanics (3.0–2.8 Ga) and the porphyries (2.8–2.7 Ga) suggest that these felsic magmas were derived by partial melting of a source that was extracted from the mantle ca. 200 Ma prior to volcanism or may indicate interaction between depleted mantle-derived melts and older crustal material. Received: 15 August 1995 / Accepted: 12 January 1996     

Crustal Evolution of Island-Arc Ultramafic Magma: Galmoenan Pyroxenite-Dunite Plutonic Complex, Koryak Highland (Far East Russia)

Alaskan-type platinum-bearing plutons and potassium-enrichedmafic to ultramafic volcanic rocks are temporally and spatiallyassociated within the Late Cretaceous–Paleocene Achaivayam–Valaginskiiintra-oceanic palaeo-arc system, allochthonously present inthe Koryak Highland and Kamchatka Peninsula (Far East Russia).The compositions of the parental magmas to the Alaskan-typecomplexes are estimated using the Galmoenan plutonic complexas an example. This complex, composed of dunites, pyroxenitesand minor gabbros, is the largest (20 km³) in the system andthe best studied owing to associated platinum placer deposits.The compositions of the principal mineral phases in the Galmoenanintrusive rocks [olivine (Fo_79–92), clinopyroxene (1–3·5wt % Al₂O₃, 0·1–0·5 wt % TiO₂), and Cr-spinel(5–15 wt % Al₂O₃ and 0·3–0·7 wt %TiO₂)] are typical of liquidus assemblages in primitive island-arcmagmas in intra-oceanic settings, and closely resemble the mineralcompositions in the Achaivayam–Valaginskii ultramaficvolcanic rocks. The temporal and spatial association of intrusiveand extrusive units, and the similarity of their mineral compositions,suggest that both suites were formed from similar parental magmas.The composition of the parental magma for the Galmoenan plutonicrocks is estimated using previously reported data for the Achaivayam–Valaginskiiultramafic volcanic rocks and phenocryst-hosted melt inclusions.Quantitative simulation of crystallization of the parental magmain the Galmoenan magma chamber shows that the compositions ofthe cumulate units are best modelled by fractional crystallizationwith periodic magma replenishment. The model calculations reproducewell the observed mineral assemblages and the trace elementabundances in clinopyroxene. Based upon the estimated compositionof the parental magmas and their mantle source, we considerthat fluxing of a highly refractory mantle wedge (similar tothe source of boninites) by chlorine-rich aqueous fluids isprimarily responsible for both high degrees of partial meltingand the geochemical characteristics of the magmas, includingtheir enrichment in platinum-group elements. KEY WORDS: subduction; platinum-group elements; clinopyroxene; trace elements; fractional crystallization; Alaskan-type plutons     

Enriched End-member of Primitive MORB Melts: Petrology and Geochemistry of Glasses from Macquarie Island (SW Pacific)

Macquarie Island is an exposure above sea-level of part of thecrest of the Macquarie Ridge. The ridge marks the Australia–Pacificplate boundary south of New Zealand, where the plate boundaryhas evolved progressively since Eocene times from an oceanicspreading system into a system of long transform faults linkedby short spreading segments, and currently into a right-lateralstrike-slip plate boundary. The rocks of Macquarie Island wereformed during spreading at this plate boundary in Miocene times,and include intrusive rocks (mantle and cumulate peridotites,gabbros, sheeted dolerite dyke complexes), volcanic rocks (N-to E-MORB pillow lavas, picrites, breccias, hyaloclastites),and associated sediments. A set of Macquarie Island basalticglasses has been analysed by electron microprobe for major elements,S, Cl and F; by Fourier transform infrared spectroscopy forH₂O; by laser ablation–inductively coupled plasma massspectrometry for trace elements; and by secondary ion mass spectrometryfor Sr, Nd and Pb isotopes. An outstanding compositional featureof the data set (47·4–51·1 wt % SiO₂, 5·65–8·75wt % MgO) is the broad range of K₂O (0·1–1·8wt %) and the strong positive covariation of K₂O with otherincompatible minor and trace elements (e.g. TiO₂ 0·97–2·1%;Na₂O 2·4–4·3%; P₂O₅ 0·08–0·7%;H₂O 0·25–1·5%; La 4·3–46·6ppm). The extent of enrichment in incompatible elements in glassescorrelates positively with isotopic ratios of Sr (⁸⁷Sr/⁸⁶Sr= 0·70255–0·70275) and Pb (²⁰⁶Pb/²⁰⁴Pb =18·951–19·493; ²⁰⁷Pb/²⁰⁴Pb = 15·528–15·589;²⁰⁸Pb/²⁰⁴Pb = 38·523–38·979), and negativelywith Nd (¹⁴³Nd/¹⁴⁴Nd = 0·51310–0·51304).Macquarie Island basaltic glasses are divided into two compositionalgroups according to their mg-number–K₂O relationships.Near-primitive basaltic glasses (Group I) have the highest mg-number(63–69), and high Al₂O₃ and CaO contents at a given K₂Ocontent, and carry microphenocrysts of primitive olivine (Fo_86–89·5).Their bulk compositions are used to calculate primary melt compositionsin equilibrium with the most magnesian Macquarie Island olivines(Fo_90·5). Fractionated, Group II, basaltic glasses aresaturated with olivine + plagioclase ± clinopyroxene,and have lower mg-number (57–67), and relatively low Al₂O₃and CaO contents. Group I glasses define a seriate variationwithin the compositional spectrum of MORB, and extend the compositionalrange from N-MORB compositions to enriched compositions thatrepresent a new primitive enriched MORB end-member. Comparedwith N-MORB, this new end-member is characterized by relativelylow contents of MgO, FeO, SiO₂ and CaO, coupled with high contentsof Al₂O₃, TiO₂, Na₂O, P₂O₅, K₂O and incompatible trace elements,and has the most radiogenic Sr and Pb regional isotope composition.These unusual melt compositions could have been generated bylow-degree partial melting of an enriched mantle peridotitesource, and were erupted without significant mixing with commonN-MORB magmas. The mantle in the Macquarie Island region musthave been enriched and heterogeneous on a very fine scale. Wesuggest that the mantle enrichment implicated in this studyis more likely to be a regional signature that is shared bythe Balleny Islands magmatism than directly related to the hypotheticalBalleny plume itself. KEY WORDS: mid-ocean ridge basalts; Macquarie Island; glass; petrology; geochemistry     

Depths of Partial Crystallization of H2O-bearing MORB: Phase Equilibria Simulations of Basalts at the MAR near Ascension Island (7 11{degrees}S)

Phase equilibria simulations were performed on naturally quenchedbasaltic glasses to determine crystallization conditions priorto eruption of magmas at the Mid-Atlantic Ridge (MAR) east ofAscension Island (7–11°S). The results indicate thatmid-ocean ridge basalt (MORB) magmas beneath different segmentsof the MAR have crystallized over a wide range of pressures(100–900 MPa). However, each segment seems to have a specificcrystallization history. Nearly isobaric crystallization conditions(100–300 MPa) were obtained for the geochemically enrichedMORB magmas of the central segments, whereas normal (N)-MORBmagmas of the bounding segments are characterized by polybariccrystallization conditions (200–900 MPa). In addition,our results demonstrate close to anhydrous crystallization conditionsof N-MORBs, whereas geochemically enriched MORBs were successfullymodeled in the presence of 0·4–1 wt% H₂O in theparental melts. These estimates are in agreement with direct(Fourier transform IR) measurements of H₂O abundances in basalticglasses and melt inclusions for selected samples. Water contentsdetermined in the parental melts are in the range 0·04–0·09and 0·30–0·55 wt% H₂O for depleted and enrichedMORBs, respectively. Our results are in general agreement (within±200 MPa) with previous approaches used to evaluate pressureestimates in MORB. However, the determination of pre-eruptiveconditions of MORBs, including temperature and water contentin addition to pressure, requires the improvement of magma crystallizationmodels to simulate liquid lines of descent in the presence ofsmall amounts of water. KEY WORDS: MORB; Mid-Atlantic Ridge; depth of crystallization; water abundances; phase equilibria calculations; cotectic crystallization; pressure estimates; polybaric fractionation     

Trace Element and Sr-Pb-Nd-Hf Isotope Evidence for Ancient, Fluid-Dominated Enrichment of the Source of Aldan Shield Lamproites

A phase of Mesozoic extension associated with the terminationof continental collision at the southern margin of the AldanShield produced ultrabasic lamproites in a discontinuous belt500 km long and 150 km wide. The lamproites, locally poorlydiamondiferous, were emplaced as dykes, sills and pipes. AllAldan lamproites have primitive chemical characteristics (e.g.MgO up to 22·7 wt %) and are ultrapotassic (K₂O up to8·3 wt %) and peralkaline with K₂O + Na₂O/Al₂O₃ in therange 0·6–1·16. A distinctive feature ofthese rocks is their low TiO₂ content (0·5–1·4wt %). Aldan lamproites are moderately light rare earth element(LREE) enriched with (La/Yb)_N ranging from 10 to 47. Heavy rareearth element (HREE) abundances are lower than for all otherlamproites by up to a factor of five. Therefore, the combinedmajor and trace element characteristics of the Aldan samplesare not typical of other lamproite occurrences. Large ion lithophileelement concentrations are high (100–800 x Primitive Mantle)but the high field strength elements (HFSE; Nb, Ta, Ti) plusTh and U display unusually low concentrations for rocks of thistype. The style of trace element enrichment recorded by theAldan Shield lamproites is comparable with that of subduction-relatedmagmatism. The Aldan lamproites have among the most extremeinitial isotopic ratios yet recorded from mantle-derived magmas;_Ndi = –10·3 to –22·3, ⁸⁷Sr/⁸⁶Sr_i =0·7055–0·7079, _Hfi = –7·6 to–29·4 and ²⁰⁶Pb/²⁰⁴Pb_i = 16·6–17·4.When interpreted in terms of multi-stage Pb isotope evolution,the Pb isotope data require fractionation from a Bulk Earthreservoir at 3·0 Ga and subsequent evolution with second-stageµ values between 6·4 and 8·0. The inferredArchaean age of the lamproite source is consistent with Nd andHf model ages, which range from 1·5 to 3·0 Ga.Aldan lamproites have _Hf values that range from +3 to –7.Trace element and Sr–Nd–Pb–Hf isotopic ratiosshow coherent variations that suggest that Archaean source enrichmentproduced the negative _Hf as a result of metasomatism by slab-derivedhydrous melts that left rutile–garnet-bearing residua.We conclude that relatively large degrees of partial meltingproduced the lamproites (>5%), which explains the preservationof the isotope–trace element correlations and the lowREE contents. Although high-quality trace element data (e.g.HFSE) are not available for most lamproites, it appears thatmany of their source regions contain a component of recycledoceanic crust, possibly including subducted sediment. The sourcesof the Aldan and many other lamproites are distinct from oceanisland basalt mantle sources. This suggests that the long-termstorage of trace element enriched lamproite sources occurredin the sub-continental lithospheric mantle and not at depthwithin the convecting asthenosphere. KEY WORDS: potassic volcanism; isotope geochemistry; fluid enrichment     

Evolution and Genesis of Magmas from Vico Volcano, Central Italy: Multiple Differentiation Pathways and Variable Parental Magmas

Vico volcano has erupted potassic and ultrapotassic magmas,ranging from silica-saturated to silica-undersaturated types,in three distinct volcanic periods over the past 0·5Myr. During Period I magma compositions changed from latiteto trachyte and rhyolite, with minor phono-tephrite; duringPeriods II and III the erupted magmas were primarly phono-tephriteto tephri-phonolite and phonolite; however, magmatic episodesinvolving leucite-free eruptives with latitic, trachytic andolivine latitic compositions also occurred. In Period II, leucite-bearingmagmas (⁸⁷Sr/⁸⁶Sr_initial = 0·71037–0·71115)were derived from a primitive tephrite parental magma. Modellingof phonolites with different modal plagioclase and Sr contentsindicates that low-Sr phonolitic lavas differentiated from tephri-phonoliteby fractional crystallization of 7% olivine + 27% clinopyroxene+ 54% plagioclase + 10% Fe–Ti oxides + 4% apatite at lowpressure, whereas high-Sr phonolitic lavas were generated byfractional crystallization at higher pressure. More differentiatedphonolites were generated from the parental magma of the high-Srphonolitic tephra by fractional crystallization of 10–29%clinopyroxene + 12–15% plagioclase + 44–67% sanidine+ 2–4% phlogopite + 1–3% apatite + 7–10% Fe–Tioxides. In contrast, leucite-bearing rocks of Period III (⁸⁷Sr/⁸⁶Sr_initial= 0·70812–0·70948) were derived from a potassictrachybasalt by assimilation–fractional crystallizationwith 20–40% of solid removed and r = 0·4–0·5(where r is assimilation rate/crystallization rate) at differentpressures. Silica-saturated magmas of Period II (⁸⁷Sr/⁸⁶Sr_initial= 0·71044–0·71052) appear to have been generatedfrom an olivine latite similar to some of the youngest eruptedproducts. A primitive tephrite, a potassic trachybasalt andan olivine latite are inferred to be the parental magmas atVico. These magmas were generated by partial melting of a veinedlithospheric mantle sources with different vein–peridotite/wall-rockproportions, amount of residual apatite and distinct isolationtimes for the veins. KEY WORDS: isotope and trace element geochemistry; polybaric differentiation; veined mantle; potassic and ultrapotassic rocks; Vico volcano; central Italy     

Geochronology and Petrogenesis of the Cretaceous Antampombato-Ambatovy Complex and Associated Dyke Swarm, Madagascar

The Antampombato–Ambatovy complex is the largest intrusionin the central–eastern part of the Cretaceous flood basaltprovince of Madagascar, with an exposed surface area of about80 km². It has an ⁴⁰Ar/³⁹Ar incremental heating age of 89·9± 0·4 Ma and a U–Pb age of 90 ± 2Ma. The outcropping plutonic rocks range from dunite and wehrlite,through clinopyroxenite and gabbro, to sodic syenite. A dykeswarm cross-cutting some of the above lithologies (and the nearbyPrecambrian basement rocks) is formed of picritic basalts, alkalito transitional basalts, benmoreites and rhyolites; some ofthe latter are peralkaline. A few basaltic dykes have cumulateolivine textures, with up to 26 wt % MgO and 1200 ppm Ni, whereasothers have characteristics more akin to those of primitiveliquids (9 wt % MgO; Mg-number 0·61; 500 ppm Cr; 200ppm Ni). These basalts have relatively high TiO₂ (2·2wt %) and total iron (14 wt % as Fe₂O₃), and moderate contentsof Nb (10–11 ppm) and Zr (c. 100 ppm). Initial (at 90Ma) Sr- and Nd-isotope ratios of the clinopyroxenites and basaltdykes are 0·7030–0·7037 and 0·51290–0·51283,respectively. Syenites and peralkaline rhyolites have Sr- andNd-isotope ratios of 0·7037–0·7039 and 0·51271–0·51274,respectively. The data suggest derivation of the parental magmasfrom a time-integrated depleted mantle source, combined withsmall amounts of crustal contamination in the petrogenesis ofthe more evolved magmas. The isotopic compositions of the mafic–ultramaficrocks are most similar to those of the mid-ocean ridge basalt(MORB)-like igneous rocks of eastern Madagascar, and suggestthe existence of an isotopically ‘depleted’ componentin the source of the entire Madagascar province, even thoughthe Antampombato basalts are chemically unlike the lavas anddykes with the same depleted isotopic signature found in westernMadagascar. If this depleted component is plume-related, thissuggests that the plume has a broadly MORB-source mantle composition.The existence of isotopically more enriched magma types in theMadagascan province has several possible petrogenetic explanations,one of which could be the interaction of plume-related meltswith the deep lithospheric mantle beneath the island. KEY WORDS: geochronology; flood basalts; Antampombato–Ambatovy intrusion; Cretaceous; Madagascar