Primitive Magma From the Jericho Pipe, N.W.T., Canada: Constraints on Primary Kimberlite Melt Chemistry

We report the first estimates of primary kimberlite melt compositionfrom the Slave craton, based on samples of aphanitic kimberlitefrom the Jericho kimberlite pipe, N.W.T., Canada. Three samplesderive from the margins of dykes where kimberlite chilled againstwall rock (JD51, JD69 and JD82) and are shown to be texturallyconsistent with crystallization from a melt. Samples JD69 andJD82 have geochemical characteristics of primitive melts: theyhave high MgO (20–25 wt %), high mg-numbers (86–88),and high Cr (1300–1900 ppm) and Ni (800–1400 ppm)contents. They also have high contents of CO₂ (10–17 wt%). Relative to bulk macrocrystal kimberlite, they have lowermg-numbers and lower MgO but are enriched in incompatible elements(e.g. Zr, Nb and Y), because the bulk kimberlite compositionsare strongly controlled by accumulation of mantle olivine andother macrocrysts. The compositions of aphanitic kimberlitefrom Jericho are similar to melts produced experimentally bypartial melting of a carbonate-bearing garnet lherzolite. Onthe basis of these experimental data, we show that the primarymagmas from the Jericho kimberlite could represent 0·7–0·9%melting of a carbonated lherzolitic mantle source at pressuresand temperatures found in the uppermost asthenosphere to theSlave craton. The measured CO₂ contents for samples JD69 andJD82 are only slightly lower than the CO₂ contents of the correspondingexperimental melts; this suggests that the earliest hypabyssalphase of the Jericho kimberlite retained most of its originalvolatile content. As such these samples provide a minimum CO₂content for the primary kimberlite magmas from the Slave craton. KEY WORDS: kimberlite; melt; primitive; primary magma; Slave craton     

Polymetamorphism in the NE Shackleton Range, Antarctica: Constraints from Petrology and U-Pb, Sm-Nd, Rb-Sr TIMS and in situ U-Pb LA-PIMMS Dating

Metapelitic rock samples from the NE Shackleton Range, Antarctica,include garnet with contrasting zonation patterns and two agespectra. Garnet porphyroblasts in K-rich kyanite–sillimanite–staurolite–garnet–muscovite–biotite schistsfrom Lord Nunatak show prograde growth zonation, and give Sm–Ndgarnet, U–Pb monazite and Rb–Sr muscovite ages of518 ± 5, 514 ± 1 and 499 ± 12 Ma, respectively.Geothermobarometry and P–T pseudo-section calculationsin the model system CaO–Na₂O–K₂O– TiO₂–MnO–FeO–MgO–Al₂O₃–SiO₂–H₂Oare consistent with garnet growth during prograde heating from540°C/7 kbar to 650°C/7·5 kbar, and partial resorptionduring a subsequent P–T decrease to <650°C at <6kbar. All data indicate that rocks from Lord Nunatak were affectedby a single orogenic cycle. In contrast, garnet porphyroblastsin K-poor kyanite–sillimanite– staurolite–garnet–cordierite–biotite-schistsfrom Meade Nunatak show two growth stages and diffusion-controlledzonation. Two distinct age groups were obtained. Laser ablationplasma ionization multicollector mass spectrometry in situ analysesof monazite, completely enclosed by a first garnet generation,yield ages of c. 1700 Ma, whereas monazite grains in open garnetfractures and in most matrix domains give c. 500 Ma. Both agegroups are also obtained by U–Pb thermal ionization massspectrometry analyses of matrix monazite and zircon, which fallon a discordia with lower and upper intercepts at 502 ±1 and 1686 ± 2 Ma, respectively. Sm–Nd garnet datingyields an age of 1571 ± 40 Ma and Rb–Sr biotiteanalyses give an age of 504 ± 1 Ma. Integrated geochronologicaland petrological data provide evidence that rocks from MeadeNunatak underwent a polymetamorphic Barrovian-type metamorphism:(1) garnet 1 growth and subsequent diffusive garnet annealingbetween 1700 and 1570 Ma; (2) garnet 2 growth during the RossOrogeny at c. 500 Ma. During the final orogenic event the rocksexperienced peak P–T conditions of about 650°C/7·0kbar and a retrograde stage at c. 575°C/4·0 kbar. KEY WORDS: garnet microtexture; P–T pseudosection; geochronology; polymetamorphism; Shackleton Range; Antarctica     

Age, Origin and Cooling History of the Coronel Joao Sa Pluton, Bahia, Brazil

In north-east Brazil, Archean and Paleoproterozoic cratonicblocks are enclosed within a network of Brasiliano-age (0·7–0·55Ga) metasedimentary foldbelts. The unfoliated Coronel JoãoSá granodiorite pluton, which contains magmatic epidoteand strongly resorbed clinopyroxene, intrudes the SergipanoFoldbelt. Zircons yield a concordant U–Pb crystallizationage of 625 ± 2 Ma; titanite ages are approximately 621Ma. Discordant zircons suggest inheritance from at least twomagma sources of ages <1·8 and >2·2 Ga.Model calculations based on diffusion parameters and Rb–Srisotope data from separated minerals indicate that the plutoncooled at a rate of 36°C/Myr. Whole-rock element compositionsand initial Sr–Nd isotopic compositions that are heterogeneouson all length scales suggest magma mixing. Trace-element concentrationsand Nd isotope data argue against a contribution from a contemporaneousmantle-derived magma. Values of magmatic _Nd (at 625 Ma) resemblecontemporary _Nd for local supracrustal rocks and basement, compatiblewith anatexis of a crustal source. In north-east Brazil, cratonicblocks could have amalgamated with foldbelts that originatedas: (1) a mosaic of island arcs and arc basins (traditionalallochthonous model), or as (2) extensional continental sedimentarybasins (but not oceanic crust) later involved in collision (autochthonousmodel). The Coronel João Sá isotopic and chemicaldata support an autochthonous origin. KEY WORDS: Brasiliano Orogeny; granodiorite pluton; Rb–Sr isotopes, Sm–Nd isotopes; U–Pb isotopes, magma cooling rate     

Late Devonian Diamondiferous Kimberlite and Alkaline Picrite (Proto-kimberlite?) Magmatism in the Arkhangelsk Region, NW Russia

Widespread penecontemporaneous igneous activity affected NWRussia (the Kola Peninsula and adjoining areas to the SE aroundArkhangelsk) during the Late Devonian (360–380 Ma). Magmatismvaries from tholeiitic basalts, erupted in the axial regionsof former Middle Proterozoic (Riphean) rifts, to strongly alkalinerock-types on and marginal to Archaean cratons. NNE of Arkhangelskkimberlites, olivine lamproites and alkaline picrites were emplaced;all these rock-types are diamondiferous to varying extents.Higher TiO₂ (and also total Fe) distinguish predominantly mica-poorEastern Group kimberlites (TiO₂ = 2·4–3·1wt %) and spatially associated alkaline picrites (TiO₂ = 3·2–3·7wt %) from nearby micaceous Western Group kimberlites (TiO₂= 0·8–1·1 wt %). Each rock-type also hasdistinctive rare earth element (REE) patterns, and     

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     

Constraints from eclogite and MARID xenoliths on origins of mantle Zr/Hf–Nb/Ta variability

New trace-element data of rutile in kimberlite-borne ~1.85 Ga eclogite and pyroxenite xenoliths from the central Slave craton, as well as ~110 Ma MARID xenoliths from the Kaapvaal craton, provide constraints on the origins of lithospheric and sublithospheric mantle variability in high field strength element ratios. Rutiles in eclogites and pyroxenites have Zr/Hf ranging from 20 to 62 and Nb/Ta ranging from 10 to 40. Rutiles in MARID xenoliths have Zr/Hf from 24 to 33 and Nb/Ta from 10 to 41. Calculated whole-rock Zr/Hf is suprachondritic for eclogites with suggested gabbroic protoliths and subchondritic for boninite-like eclogites; the latter is consistent with cpx-controlled depletion in the protolith source. Within each eclogite type, positive correlations of Zr/Hf with La/Lu and negative correlations with Lu/Hf likely reflect fractionation of cpx and/or plagioclase during crystallisation of the protoliths. Zr/Hf–Nb/Ta relationships of some MARID-type rocks, which are products of lithospheric mantle metasomatism, and eclogite xenoliths plot on a silicate differentiation trend, whereas other samples have higher Nb/Ta at a given Zr/Hf. Fractionation of a few percent rutile from an HFSE-rich mafic melt can generate a trend towards strongly increased Nb/Ta at minimally changed Zr/Hf in the residual melt. Superposition of rutile fractionation on the effects of silicate differentiation, which fractionates Zr/Hf more strongly than Nb/Ta, can explain the Zr/Hf–Nb/Ta relationships of most eclogites from the central Slave craton as well as those of MARID rocks, metasomatised peridotites and group II kimberlites. By contrast, Zr/Hf–Nb/Ta relationships suggest that Group I kimberlites are mixtures between depleted peridotite and carbonatite. Thus, high Nb/Ta is a signature of lithospheric processes and may not be important in deeply subducted eclogites that bypass extended residence in the lithosphere. Conversely, considerable primary Zr/Hf variability was inherited by the eclogites, which is indicative of the compositional diversity of ancient subducted oceanic crust, which is expected to have generated substantial heterogeneity in sublithospheric basalt sources.     

Low-Temperature Eclogites and Eclogitic Schists in Mn-rich Metabasites in Ward Creek, California; Mn and Fe Effects on the Transition between Blueschist and Eclogite

In situ eclogitic schist lenses occur in the coherent low-gradeepidote-zone Ward Creek metabasite unit of the Central Franciscanbelt. They contain almandine garnet, clinopyroxene, and rutile.They have slightly higher Mn content (0–5–1–0wt.%) than the coexisting Type III metabasites (0–12–0–25wt%) which contain epidote + glaucophane + actinolite + chlorite+ omphacite + quartz + sphene ? aragonite? lawsonite ? pumpellyite+ albite. The in situ eclogitic schists (130–140 Ma) canbe distinguished from older tectonic eclogites (150–160Ma) in Ward Creek as follows: (1) they are medium grained, whereasType IV tectonic eclogites are coarse grained; (2) they haveunaltered spessartine-rich idioblastic (0–4–10 mm)garnets, whereas Type IV tectonic eclogites have larger xenoblasticto hypidiomorphic spessartine-poor garnets which were corrodedand chloritized along the rim during retrograde metamorphism;(3) clinopyroxenes are chloromelanite in in situ eclogitic schistsbut omphacite in Type IV tectonic eclogites; (4) barroisiticamphiboles occur both as inclusions in garnets and as matrixminerals in Type IV tectonic eclogites but not in in situ eclogiticschists; (5) albite is present in in situ eclogitic schistsbut not in Type IV tectonic eclogites; and (6) the estimatedP-T condition of in situ eclogitic schists is 290 ?C < T<350 ?C, P = 8–9 kb, whereas that of Ward Creek Type IVtectonic eclogites is 500?C< r<540?C, P< 10–11–5kb. Medium-grained eclogites occur as individual blocks in WardCreek; they are different from Type IV tectonic eclogites butare very similar to in situ eclogitic schists. They have unalteredidioblastic garnet with high almandine and spessartine content(Alm₄₇Sp₂3Gr₂₀Py10), and they have chloromel-anitic clinopyroxeneand quartz but no barroisite. Paragonite is also stable in theseeclogites. The blocks formed at 380 ?C< r<400?C, and 9–5kb<P< 14 kb. They are presumably in situ eclogites formedat the highest-temperature part of the Ward Creek metabasiteunit and may be younger than Type IV tectonic eclogites. Such low-temperature occurrences of eclogitic assemblages aredue to the compositional effect on reactions between blueschistand eclogite that are insensitive to pressure and shift towardslower temperatures as bulk-rock MnO content and X_Fe/(Fe+Mg)increase. The Mn/(Mn + Fe) ratio of bulk rock is an importantfactor in controlling the P-T positions of these reactions attemperatures below 450 ?C, whereas the Fe/(Fe + Mg) ratio ofbulk-rock becomes important at temperatures higher than 450?C.     

An Archean(?) to Paleozoic Evolution for a Garnet Peridotite Lens with Sub-Baltic Shield Affinity within the Seve Nappe Complex of Jamtland, Sweden, Central Scandinavian Caledonides

Mineralogical, isotopic, geochemical and geochronological evidencedemonstrates that the Friningen body, a garnet peridotite bodycontaining garnet pyroxenite layers in the Seve Nappe Complex(SNC) of Northern Jämtland, Sweden, represents old, certainlyProterozoic and possibly Archean, lithosphere that became incorporatedinto the Caledonian tectonic edifice during crustal subductioninto the mantle at c. 450 Ma. Both garnet peridotite and pyroxenitecontain two (M₁ and M₂) generations of garnet-bearing assemblagesseparated by the formation of two-pyroxene, spinel symplectitearound the M₁ garnet and the crystallization of low-Cr spinel_1Cin the matrix. These textures suggest initial high-pressure(HP) crystallization of garnet peridotite and pyroxenite succeededby decompression into the spinel stability field, followed byrecompression into the garnet peridotite facies. Some pyroxenitelayers appear to be characterized solely by M₂ assemblages withstretched garnet as large as several centimeters. Laser ablationmicroprobe–inductively coupled plasma mass spectrometryRe–Os analyses of single sulfide grains generally definemeaningless model ages suggesting more than one episode of Reand/or Os addition and/or loss to the body. Pentlandite grainsfrom a single polished slab of one garnet peridotite, however,define a linear array on an Re–Os isochron diagram that,if interpreted as an errorchron, suggests an Archean melt extractionevent that left behind the depleted dunite and harzburgite bodiesthat characterize the SNC. Refertilization of this mantle bymelts associated with the development of the pyroxenite layersis indicated by enriched clinopyroxene Sr–Nd isotope ratios,and by parallel large ion lithophile-enriched trace elementpatterns in clinopyroxene from pyroxenite and the immediatelyadjacent peridotite. Clinopyroxene and whole-rock model Sm–Ndages (T_DM = 1·1–2·2 Ga) indicate that fertilizationtook place in Proterozoic times. Sm–Nd garnet₂–clinopyroxene₂–wholerock ± orthopyroxene₂ mineral isochrons from three pyroxenitelayers define overlapping ages of 452·1 ± 7·5and 448 ± 13 Ma and 451 ± 43 Ma (2     

A Metamorphosed Early Cambrian Crust-Mantle Transition in the Eastern Alps, Austria

In the Speik Complex (Eastern Alps, Austria), highly melt-depleted,metamorphosed harzburgites with abundant pods and layers ofchromitite are interlayered with a suite of metamorphosed orthopyroxenites,clinopyroxenites and gabbros. Coarse-grained orthopyroxenitesoccur as centimetre- to metre-wide veinlets and pods, but alsoas intrusive plugs several tens of metres wide. Intimately associatedmetaclinopyroxenite and metagabbro are present as bodies upto several metres thick at a distinct stratigraphic level withinthe complex. In the ultramafic rocks, relict magmatic olivine,orthopyroxene, clinopyroxene and spinel have been overprintedby a metamorphic assemblage of forsterite, diopside, tremolite,anthophyllite, chlorite, serpentine, talc and Cr–Fe-richspinel. Hornblende, epidote, zoisite and chlorite dominate themetamorphic paragenesis in metagabbros, in addition to rarerelicts of clinopyroxene and two phases of Ca-rich garnet. Thepolymetamorphic evolution of the Speik Complex includes rarelypreserved pre-Variscan (400 Ma) eclogite-facies conditions,Variscan (330 Ma) amphibolite-facies conditions (600–700°C,>5 kbar) and Eoalpine (100 Ma) greenschist- to amphibolite-faciesconditions reaching 550°C and 7–10 kbar. Orthopyroxenitesare characterized by high concentrations of SiO₂, MgO and Cr,and by U-shaped chondrite-normalized rare earth element (REE)patterns similar to those of their harzburgite hosts. The REEpatterns of the clinopyroxenites are flat to slightly enrichedin light REE. Metagabbro compositions are variable, but generallycharacterized by low SiO₂ and high mg-numbers (61–78).Their REE patterns all have Gd_N/Yb_N > 1; some samples havelarge positive Eu anomalies implying the original presence ofcumulus plagioclase. In the orthopyroxenites, clinopyroxenitesand some peridotites, Pt, Pd and Re are distinctly enrichedcompared with Os, Ir and Ru, whereas most harzburgites haveunfractionated to slightly fractionated platinum-group element(PGE) patterns with respect to average upper mantle. The Re–Osisotope compositions of the pyroxenites define an errorchronat 550 ± 17 Ma and a supra-chondritic ¹⁸⁷Os/¹⁸⁸Os of0·179 ± 0·003. An isochron age of 554 ±37 Ma with _Nd(i) +0·7 is indicated by the Sm–Ndisotope compositions of whole-rock pyroxenite and gabbro samples,whereas the harzburgites plot on an errorchron of 745 ±45 Ma and _Nd(i) +6. The pyroxenites and gabbros probably representa cogenetic suite of magmatic dykes intruded into uppermost,highly depleted, suboceanic mantle below the crust–mantletransition zone in an oceanic basin close to the northwesternmargin of Gondwana. KEY WORDS: pyroxenite; metagabbro; geochemistry; Re–Os isotopes; Sm–Nd isotopes     

Continuous Gradations among Primary Carbonatitic, Kimberlitic, Melilititic, Basaltic, Picritic, and Komatiitic Melts in Equilibrium with Garnet Lherzolite at 3-8 GPa

Multianvil melting experiments in the system CaO–MgO–Al₂O₃–SiO₂–CO₂(CMAS–CO₂) at 3–8 GPa, 1340–1800°C, involvingthe garnet lherzolite phase assemblage in equilibrium with CO₂-bearingmelts, yield continuous gradations in melt composition betweencarbonatite, kimberlite, melilitite, komatiite, picrite, andbasalt melts. The phase relations encompass a divariant surfacein P–T space. Comparison of the carbonatitic melts producedat the low-temperature side of this surface with naturally occurringcarbonatites indicates that natural magnesiocarbonatites couldbe generated over a wide range of pressures >2·5 GPa.Melts analogous to kimberlites form at higher temperatures alongthe divariant surface, which suggests that kimberlite genesisrequires more elevated geotherms. However, the amount of waterfound in some kimberlites has the potential to lower temperaturesfor the generation of kimberlitic melts by up to 150°C,provided no hydrous phases are present. Compositions resemblinggroup IB and IA kimberlites are produced at pressures around5–6 GPa and 10 GPa, respectively, whereas the compositionsof some other kimberlites suggest generation at higher pressuresstill. At pressures <4 GPa, an elevated geotherm producesmelilitite-like melt in the CMAS–CO₂ system rather thankimberlite. Even when a relatively CO₂-rich mantle compositioncontaining 0·15 wt % CO₂ is assumed, kimberlites andmelilitites are produced by <1% melting and carbonatitesare generated by even smaller degrees of melting of <0·5%. KEY WORDS: carbonatite; CO₂; kimberlite; melilitite; melt generation     

Diamonds and eclogites of the Jericho kimberlite (Northern Canada)

We studied diamonds and barren and diamondiferous eclogite xenoliths from the Jericho kimberlite (Northern Slave craton). The majority of the diamonds are non-resorbed octahedral crystals, with moderately aggregated N (IaB < 50%, N < 300 ppm) and δ¹³C = −5 to −41‰. The diamonds belong to “eclogitic” (90% of the studied samples), “websteritic” (7%) and “peridotitic” (3%) assemblages. The Jericho diamonds differ from the majority of “eclogitic” diamonds worldwide in magnesian compositions of associated minerals and extremely light C isotopic compositions (δ¹³C = −24 to −41‰). We propose that metasomatism triggered by H₂O fluids may have been involved in the diamond formation. Multiple episodes of the metasomatism and associated melt extraction of various ages are evident in Jericho eclogite xenoliths where primary garnet and clinopyroxene have been recrystallized to more magnesian minerals with higher contents of some incompatible trace elements and to hydrous secondary phases. The model is supported by the general similarity of mineral compositions in diamondiferous eclogites to those in diamond inclusions and to secondary magnesian garnet and clinopyroxene in recrystallized barren eclogites. The ultimate products of the metasomatism could be “websteritic” diamond assemblages sourced from magnesian eclogites. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

A 2.5 ka History of Dacitic Magmatism at Nevado de Toluca, Mexico: Petrological, 40Ar/39Ar Dating, and Experimental Constraints on Petrogenesis

After 11·5 ka of quiescence (24·5–13 ka),the Nevado de Toluca volcano started a 2500 year period of activity.This period was characterized by a dome destruction event at13 ka, a small Plinian event at 12·1 ka, and a largePlinian eruption at 10·5 ka. About 10 km³ of magma waserupted that was homogeneous in composition (63·3–65·7SiO₂ wt % whole-rock) and in mineralogy. Pumice consists ofplagioclase (An_30–59) > orthopyroxene (En_56–59)> hornblende >> Fe–Ti oxides + rare apatite (inopx) + biotite, set in a rhyolitic matrix (72–76 SiO₂wt %). ⁴⁰Ar/³⁹Ar analysis of single biotite crystals yieldedages (0·81–4·7 Ma), that do not correspondto eruption ages. The biotite represents partially assimilatedxenocrysts, which could have resided in the magma for only ashort period of time. Mineral chemical data, coupled with hydrothermalexperiments, indicate that prior to eruption the dacitic magmastagnated at a depth of 4·5–6 km below the summitat water pressures of 160–210 MPa and a temperature of824 ± 12°C on the basis of Fe–Ti oxide thermometry,and under water-saturated conditions. To stabilize a homogeneousmagma body of >10 km³ at 824°C in the upper crust, wepropose that reheating of the dacitic reservoir by hotter magmabatches was able to maintain the equilibrium between the temperatureof the magma and the assimilation of wall-rock over a periodof 2500 years. Based on similarities among the juvenile products,we suggest that the three eruptions were fed from the same magmabody. KEY WORDS: explosive volcanism; xenocrystic contamination; Nevado de Toluca, Mexico     

Genesis of Ultramafic Lamprophyres and Carbonatites at Aillik Bay, Labrador: a Consequence of Incipient Lithospheric Thinning beneath the North Atlantic Craton

Numerous dykes of ultramafic lamprophyre (aillikite, mela-aillikite,damtjernite) and subordinate dolomite-bearing carbonatite withU–Pb perovskite emplacement ages of 590–555 Ma occurin the vicinity of Aillik Bay, coastal Labrador. The ultramaficlamprophyres principally consist of olivine and phlogopite phenocrystsin a carbonate- or clinopyroxene-dominated groundmass. Ti-richprimary garnet (kimzeyite and Ti-andradite) typically occursat the aillikite type locality and is considered diagnosticfor ultramafic lamprophyre–carbonatite suites. Titanianaluminous phlogopite and clinopyroxene, as well as comparativelyAl-enriched but Cr–Mg-poor spinel (Cr-number < 0.85),are compositionally distinct from analogous minerals in kimberlites,orangeites and olivine lamproites, indicating different magmageneses. The Aillik Bay ultramafic lamprophyres and carbonatiteshave variable but overlapping ⁸⁷Sr/⁸⁶Sr_i ratios (0·70369–0·70662)and show a narrow range in initial _Nd (+0·1 to +1·9)implying that they are related to a common type of parentalmagma with variable isotopic characteristics. Aillikite is closestto this primary magma composition in terms of MgO (15–20wt %) and Ni (200–574 ppm) content; the abundant groundmasscarbonate has ¹³C_PDB between –5·7 and –5,similar to primary mantle-derived carbonates, and ¹⁸O_SMOW from9·4 to 11·6. Extensive melting of a garnet peridotitesource region containing carbonate- and phlogopite-rich veinsat 4–7 GPa triggered by enhanced lithospheric extensioncan account for the volatile-bearing, potassic, incompatibleelement enriched and MgO-rich nature of the proto-aillikitemagma. It is argued that low-degree potassic silicate to carbonatiticmelts from upwelling asthenosphere infiltrated the cold baseof the stretched lithosphere and solidified as veins, therebycrystallizing calcite and phlogopite that were not in equilibriumwith peridotite. Continued Late Neoproterozoic lithosphericthinning, with progressive upwelling of the asthenosphere beneatha developing rift branch in this part of the North Atlanticcraton, caused further veining and successive remelting of veinsplus volatile-fluxed melting of the host fertile garnet peridotite,giving rise to long-lasting hybrid ultramafic lamprophyre magmaproduction in conjunction with the break-up of the Rodinia supercontinent.Proto-aillikite magma reached the surface only after coatingthe uppermost mantle conduits with glimmeritic material, whichcaused minor alkali loss. At intrusion level, carbonate separationfrom this aillikite magma resulted in fractionated dolomite-bearingcarbonatites (¹³C_PDB –3·7 to –2·7)and carbonate-poor mela-aillikite residues. Damtjernites maybe explained by liquid exsolution from alkali-rich proto-aillikitemagma batches that moved through previously reaction-lined conduitsat uppermost mantle depths. KEY WORDS: liquid immiscibility; mantle-derived magmas; metasomatism, Sr–Nd isotopes; U–Pb geochronology     

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     

Tracing the high pressure stage in the polymetamorphic Texel Complex (Austroalpine basement unit, Eastern Alps): P–T–t–d constraints

Summary Integration of new mineral chemical, geochronological and structural data from the Texel Complex yielded information on (re)crystallization and deformation processes in metapelites, eclogites and tonalitic orthogneisses during eclogite facies metamorphism. Maximum P–T conditions reached 1.2 to 1.4 GPa and 540–620 °C in the Upper Cretaceous. In tonalitic orthogneisses and metapelites, substantial garnet growth took place prior to eclogite facies metamorphism and Sm–Nd data indicate the presence of pre-Cretaceous mineral relics. In contrast, complex garnet-growth and -resorption processes are inferred for eclogites, which produced characteristic atoll microstructures and occurred close to the pressure peak of a single, coherent high pressure event. Garnet Sm–Nd data indicate eclogite facies crystallization at 85 ± 5 Ma. While eclogites retained information on the maximum burial stage, matrix phases in metapelites and orthogneisses were intensely recrystallized during the amphibolite facies metamorphic decompression. All the meso- and macro-scale deformation structures formed during the high pressure event and subsequent exhumation. The major mylonitic foliation is represented by the high pressure phases but was refolded during amphibolite facies exhumation. A biotite-whole-rock Rb–Sr age of 70–80 Ma indicates that cooling below about 300 °C occurred in the Upper Cretaceous. Supplementary material to this paper is available in electronic form at Appendix available as electronic supplementary material     

Monazite-Xenotime Thermochronometry and Al2SiO5 Reaction Textures in the Picuris Range, Northern New Mexico, USA: New Evidence for a 1450-1400 Ma Orogenic Event

Al₂SiO₅ reaction textures in aluminous schist and quartziteof the northern Picuris range, north-central New Mexico, recorda paragenetic sequence of kyanite to sillimanite to andalusite,consistent with a clockwise P–T loop, with minor decompressionnear the Al₂SiO₅ triple-point. Peak metamorphic temperaturesare estimated at 510–525°C, at 4·0–4·2kbar. Kyanite and fibrolite are strongly deformed; some prismaticsillimanite, and all andalusite are relatively undeformed. Monaziteoccurs as inclusions within kyanite, mats of sillimanite andcentimetre-scale porphyroblasts of andalusite, and is typicallyaligned subparallel to the dominant regional foliation (S₀/S₁or S₂) and extension lineation (L₁). Back-scatter electron imagesand X-ray maps of monazite reveal distinct core, intermediateand rim compositional domains. Monazite–xenotime thermometryfrom the intermediate and rim domains yields temperatures of405–470°C (±50°C) and 500–520°C(±50°C), respectively, consistent with the progradeto peak metamorphic growth of monazite. In situ, ion microprobeanalyses from five monazites yield an upper intercept age of1417 ± 9 Ma. Near-concordant to concordant analyses yield²⁰⁷Pb–²⁰⁶Pb ages from 1434 ± 12 Ma (core) to 1390± 20 Ma (rim). We find no evidence of older regionalmetamorphism related to the 1650 Ma Mazatzal Orogeny. KEY WORDS: Al₂SiO₅; metamorphism; monazite; thermochronometry; triple-point     

The Origins of Yakutian Eclogite Xenoliths

Owing to the association with diamonds, eclogite xenoliths havereceived disproportionate attention given their low abundancein kimberlites. Several hypotheses have been advanced for theorigin of eclogite xenoliths, from the subduction and high-pressuremelting of oceanic crust, to cumulates and liquids derived fromthe upper mantle. We have amassed a comprehensive data set,including major- and trace-element mineral chemistry, carbonisotopes in diamonds, and Rb–Sr, Sm–Nd, Re–Os,and oxygen isotopes in ultrapure mineral and whole-rock splitsfrom eclogites of the Udachnaya kimberlite pipe, Yakutia, Russia.Furthermore, eclogites from two other Yakutian kimberlite pipes,Mir and Obnazhennaya, have been studied in detail and offercontrasting images of eclogite protoliths. Relative to eclogitesfrom southern Africa and other Yakutian localities, Udachnayaeclogites are notable in the absence of chemical zoning in mineralgrains, as well as the degree of light rare earth element (LREE)depletion and unradiogenic Sr; lack of significant oxygen, sulfur,and carbon isotopic variation relative to the mantle; and intermineralradiogenic isotopic equilibration. Several of these eclogitescould be derived from ancient, recycled, oceanic crust, butmany others exhibit no evidence for an oceanic crustal protolith.The apparent lack of stable-isotope variation in the Udachnayaeclogites could be due to the antiquity of the samples and consequentlack of deep oceanic and biogenically diverse environments atthat time. Those eclogites that are interpreted to be non-recycledhave compositions characteristic of Group A eclogites from otherlocalities that also have been interpreted as being directlyfrom the mantle. At least two separate and diverse isotopicreservoirs are suggested by Nd isotopic whole-rock reconstructions.Most samples were derived from typical depleted mantle. However,two groups of three samples each indicate both enriched mantleand possible ultra-depleted mantle present beneath Yakutia duringthe late Archean and early Proterozoic. The vast majority ofeclogites studied from the Obnazhennaya pipe also exhibit characteristicsof Group A eclogites and are probably derived directly fromthe mantle. However, the eclogites from the Mir kimberlite aremore typical of other eclogites world-wide and show convincingevidence of a recycled, oceanic crustal affinity. We concurwith the late Ted Ringwood that eclogites can be formed in avariety of ways, both within the mantle and from oceanic crustalresidues. KEY WORDS: diamonds; eclogite xenoliths; isotopic composition; REE; Yakutia     

Petrology and Geochemistry of Eclogite Xenoliths from the Colorado Plateau: Implications for the Evolution of Subducted Oceanic Crust

Eclogite xenoliths from the Colorado Plateau, interpreted asfragments of the subducted Farallon plate, are used to constrainthe trace element and Sr–Nd–Pb isotopic compositionsof oceanic crust subducted into the upper mantle. The xenolithsconsist of almandine-rich garnet, Na-clinopyroxene, lawsoniteand zoisite with minor amounts of phengite, rutile, pyrite andzircon. They have essentially basaltic bulk-rock major elementcompositions; their Na₂O contents are significantly elevated,but K₂O contents are similar to those of unaltered mid-oceanridge basalt (MORB). These alkali element characteristics areexplained by spilitization or albitization processes on thesea floor and during subduction-zone metasomatism in the fore-arcregion. The whole-rock trace element abundances of the xenolithsare variable relative to sea-floor-altered MORB, except forthe restricted Zr/Hf ratios (36·9–37·6).Whole-rock mass balances for two Colorado Plateau eclogite xenolithsare examined for 22 trace elements, Rb, Cs, Sr, Ba, Y, rareearth elements, Pb, Th and U. Mass balance considerations andmineralogical observations indicate that the whole-rock chemistriesof the xenoliths were modified by near-surface processes afteremplacement and limited interaction with their host rock, aserpentinized ultramafic microbreccia. To avoid these secondaryeffects, the Sr, Nd and Pb isotopic compositions of mineralsseparated from the xenoliths were measured, yielding 0·70453–0·70590for ⁸⁷Sr/⁸⁶Sr, –3·1 to 0·5 for Nd and 18·928–19·063for ²⁰⁶Pb/²⁰⁴Pb. These isotopic compositions are distinctlymore radiogenic for Sr and Pb and less radiogenic for Nd thanthose of altered MORB. Our results suggest that the MORB-likeprotolith of the xenoliths was metasomatized by a fluid equilibratedwith sediment in the fore-arc region of a subduction zone andthat this metasomatic fluid produced continental crust-likeisotopic compositions of the xenoliths. KEY WORDS: Colorado Plateau; eclogite xenolith; geochemistry; subducted oceanic crust     

Calculated Phase Relations in the System Na2O-CaO-K2O-FeO-MgO-Al2O3-SiO2-H2O with Applications to UHP Eclogites and Whiteschists

Pressure–temperature grids in the system Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O and its subsystems have been calculatedin the range 15–45 kbar and 550–900°C, usingan internally consistent thermodynamic dataset and new thermodynamicmodels for amphibole, white mica, and clinopyroxene, with thesoftware THERMOCALC. Minerals considered for the grids includegarnet, omphacite, diopside, jadeite, hornblende, actinolite,glaucophane, zoisite, lawsonite, kyanite, coesite, quartz, talc,muscovite, paragonite, biotite, chlorite, and plagioclase. Compatibilitydiagrams are used to illustrate the phase relationships in thegrids. Coesite-bearing eclogites and a whiteschist from Chinaare used to demonstrate the ability of pseudosections to modelphase relationships in natural ultrahigh-pressure metamorphicrocks. Under water-saturated conditions, chlorite-bearing assemblagesin Mg- and Al-rich eclogites are stable at lower temperaturesthan in Fe-rich eclogites. The relative temperature stabilityof the three amphiboles is hornblende > actinolite > glaucophane(amphibole names used sensu lato). Talc-bearing assemblagesare stable only at low temperature and high pressure in Mg-and Al-rich eclogites. For most eclogite compositions, talccoexists with lawsonite, but not zoisite, in the stability fieldof coesite. Water content contouring of pressure–temperaturepseudosections, along with appropriate geotherms, provides newconstraints concerning dehydration of such rocks in subductingslabs. Chlorite and lawsonite are two important H₂O-carriersin subducting slabs. Depending on bulk composition and pressure–temperaturepath, amphibole may or may not be a major H₂O-carrier to depth.In most cases, dehydration to make ultrahigh-pressure eclogitestakes place gradually, with H₂O content controlled by divariantor higher variance assemblages. Therefore, fluid fluxes in subductionzones are likely to be continuous, with the rate of dehydrationchanging with changing pressure and temperature. Further, eclogitesof different bulk compositions dehydrate differently. Dehydrationof Fe-rich eclogite is nearly complete at relatively shallowdepth, whereas Mg- and Al-rich eclogites dehydrate continuouslydown to greater depth. KEY WORDS: dehydration; eclogites; phase relations; THERMOCALC; UHP metamorphism; whiteschists     

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