Low temperature,low pressure deformation and metamorphism of the Vangorda massive sulphide orebody,Yukon, Canada

The Vangorda orebody is a small stratiform massive sulphide orebody located in Anvil District, Yukon, Canada. The orebody consists of fineto medium-grained semi-massive and massive sulphides with a common sulphide mineralogy of pyrite, pyrrhotite, sphalerite, galena, and minor chalcopyrite. The host rocks and the sulphide lithofacies have been complexly deformed during two phases of deformation (D₁ and D₂) and associated metamorphism (M₁ and M₂). The effects of d₁ and M₁ are penetratively overprinted by D₂ and M₂. D₂ and M₂ resulted in tight to isoclinal F₂ folding of the orebody, remobilisation of the sulphides, recrystallisation and development of shear zones along the limbs of the F₂ folds. Chlorite thermometry and sulphide thermobarometry have been carried out on the host phyllites and on the sulphides. Chlorite was analysed from the S₁ and S₂ foliations in the phyllites to determine M₁ and M₂ temperatures, respectively. However, no difference was found between chlorite compositions in these foliations and a mean temperature of 363 °C was calculated from the tetrahedral A1_IV occupancy. Arsenopyrite thermometry yielded a comparable mean temperature of 336 °C. Sphalerite inclusions in M₂ pyrite porphyroblasts from D₂ shear zones were analysed for pressure using the sphalerite + hexagonal pyrrhotite + pyrite barometer. Inclusions were analysed in an attempt to determine if relic m₁ sphalerite, and hence pressure signature, was preserved. Inclusion compositions appear to reflect only M₂ conditions and yielded a mean pressure of 4.0 kb. Sphalerite + hexagonal pyrrhotite assemblages were analysed from D₂ shear zones to determine the M₂ pressure using the sphalerite + hexagonal pyrrhotite barometer. These calculations yielded a mean pressure of 6.1 kb. The M₂ temperatures and pressures calculated using these calibrations are in good agreement with those estimated from petrogenetic relationships.     

Bayes estimation: A novel approach to derivation of internally consistent thermodynamic data for minerals,their uncertainties,and correlations. Part II: Application

Internally consistent thermodynamic data, including their uncertainties and correlations, are reported for 22 phases of the quaternary system CaO-Al₂O₃-SiO₂-H₂O. These data have been derived by simultaneous evaluation of the appropriate phase properties (PP) and reaction properties (RP) by the novel technique of Bayes estimation (BE). The thermodynamic model used and the theory of BE was expounded in Part I of this paper. Part II is the follow-up study illustrating an application of BE. The input for BE comprised, among others, the a priori values for standard enthalpy of formation of the i-th phase, Δ_f H _i ⁰ , and its standard entropy, S _i ⁰ , in addition to the reaction reversal constraints for 33 equilibria involving the relevant phases. A total of 269 RP restrictions have been processed, of which 107 turned out to be non-redundant. The refined values for Δ_f H _i ⁰ and S _i ⁰ obtained by BE, including their 2σ-uncertainties, appear in Table 4; the Appendix reproduces the corresponding correlation matrix. These data permit generation of computed phase diagrams with 2σ-uncertainty envelopes based on conventional error propagation; Fig. 3 depicts such a phase diagram for the system CaO-Al₂O₃-SiO₂. It shows that the refined dataset is capable of yielding phase diagrams with uncertainty envelopes narrow enough to be geologically useful. The results in Table 4 demonstrate that the uncertainties of the prior values for Δ_f H _i ^Emphasis>0 , given in Table 1, have decreased by up to an order of magnitude, while those for S _i ⁰ improved by a factor of up to two. For comparison, Table 4 also lists the refined Δ_f H _i ⁰ and S _i ⁰ data obtained by mathematical programming (MAP), minimizing a quadratic objective function used earlier by Berman (1988). Examples of calculated phase diagrams are given to demonstrate the advantages of BE for deriving internally consistent thermodynamic data. Although P-T curves generated from both MAP and BE databases will pass through the reversal restrictions, BE datasets appear to be better suited for extrapolations beyond the P-T range explored experimentally and for predicting equilibria not constrained by reversals.     

Silicate melts at magmatic temperatures: in-situ structure determination to 1651°C and effect of temperature and bulk composition on the mixing behavior of structural units

The abundance of coexisting structural units in K-, Na-, and Li-silicate melts and glasses from 25° to 1654°C has been determined with in-situ micro-Raman spectroscopy. From these data an equilibrium constant, K_x, for the disproportionation reaction among the structural units coexisting in the melts, Si₂O₅(2Q³)SiO₃(Q²)+SiO₂(Q⁴), was calculated (K_x is the equilibrium constant derived by using mol fractions rather than activities of the structural units). From ln K_x vs l/T relationships the enthalpy (H_x) for the disproportionation reaction is in the range of-30 to 30 kJ/mol with systematic compositional dependence. In the potassium and sodium systems, where the disproportionation reaction shifts to the right with increasing temperature, the H_x increases with silica content (M/Si decreases, M=Na, K). For melts and supercooled liquids of composition Li₂O·2SiO₂ (Li/Si=1), the H_x is indistinguishable from 0. By decreasing the Li/Si to 0.667 (composition LS3) and beyond (e.g., LS4), the disproportionation reaction shifts to the left as the temperature is increased. For a given ratio of M/Si (M=K, Na, Li), there is a positive, near linear correlation between the H_x and the Z/r² of the metal cation. The slope of the H_x vs Z/r² regression lines increases as the system becomes more silica rich (i.e., M/Si is decreased). Activity coefficients for the individual structural units, _i, were calculated from the structural data combined with liquidus phase relations. These coefficients are linear functions of their mol fraction of the form _i=a lnX _i+b, where a is between 0.6 and 0.87, and X _i is the mol fraction of the unit. The value of the intercept, b, is near 0. The relationship between activity coefficients and abundance of individual structural units is not affected by temperature or the electronic properties of the alkali metal. The activity of the structural units, however, depend on their concentration, type of metal cation, and on temperature.     

Pb−Sr−Nd−O isotopic constraints on the origin of rhyolites from the Taupo Volcanic Zone of New Zealand: evidence for assimilation followed by fractionation from basalt

A comprehensive Sr–Nd–Pb–O isotopic study is reported for rhyolites from the Maroa Volcanic Centre in the Taupo Volcanic Zone (TVZ) of New Zealand. The Sr–Nd isotopic compositions of the rhyolites (⁸⁷Sr/⁸⁶Sr=0.705236 to 0.705660 and _Nd = 2.0 to 0.2) are intermediate between those of primitive basalts (⁸⁷Sr/⁸⁶Sr=0.70387 and _Nd = 5.3) and the Torlesse basement (⁸⁷Sr/⁸⁶Sr=0.709 and _Nd = -4.5). The relatively low mantle-like oxygen isotopic compositions of ¹⁸ O = 7 ± 0.5 are consistent with the Nd-Sr isotopic constraints in that they can be accounted for by 15% to 25% crustal contamination of a basaltic parent by relatively ¹⁸ O-rich Torlesse metasediment. High precision Pb isotopic analyses of plagioclase separates from the Maroa rhyolites show that they have essentially the same compositions as the Torlesse metasedimentary terrane which is itself distinctive from the Western or Waipapa metasediments. Due to the high concentration of Pb in the Torlesse metasediments (>20 ppm) compared to the basalts (<2 ppm), the Pb isotopic composition of the volcanics may be controlled by relatively small amounts (>10%) of crustal contamination. All these results are shown to be consistent with derivation of the rhyolites by 15% to 25% contamination of relatively primitive basaltic magmas with Torlesse metasedimentary crust, followed by extensive, essentially closed system fractionation of the basalt to a magma of rhyolite composition. It is argued that the processes of assimilation and fractionation are separated in both space and time. The voluminous high silica rhyolites, which make up >97% of the exposed volcanism in the continental margin back-are basin environment of the TVZ, therefore appear to be a product of predominantly new additions to the crust with assimilation-recycling of pre-existing crust being of secondary importance.     

Aqueous alteration of the Bali CV3 chondrite: evidence from mineralogy, mineral chemistry, and oxygen isotopic compositions

A petrographic, geochemical, and oxygen isotopic study of the Bali CV3 carbonaceous chondrite revealed that the meteorite has undergone extensive deformation and aqueous alteration on its parent body. Deformation textures are common and include flattened chondrules, a well-developed foliation, and the presence of distinctive (100) planar defects in olivine. The occurrence of alteration products associated with the planar defects indicates that the deformation features formed prior to the episode of aqueous alteration. The secondary minerals produced during the alteration event include well-crystallized Mg-rich saponite, framboidal magnetite, and Ca-phosphates. The alteration products are not homogeneously distributed throughout the meteorite, but occur in regions adjacent to relatively unaltered material, such as veins of altered material following the foliation. The alteration assemblage formed under oxidizing conditions at relatively low temperatures (<100 degrees C). Altered regions in Bali have higher Na, Ca, and P contents than unaltered regions which suggests that the fluid phase carried significant dissolved solids. Oxygen isotopic compositions for unaltered regions in Bali fall within the field for other CV3 whole-rocks, however, the oxygen isotopic compositions of the heavily altered material lie in the region for the CM and CR chondrites. The heavy-isotope enrichment of the altered regions in Bali suggest alteration conditions similar to those for the petrographic type-2 carbonaceous chondrites.     

Crustal Melting in the Cordilleran Interior: The Mid-Cretaceous White Creek Batholith in the Southern Canadian Cordillera

The mid-Cretaceous White Creek batholith in southeast BritishColumbia is a zoned pluton ranging from quartz monzodioriteon the margin, to hornblende-and biotite-bearing granodioritetowards the interior of the batholith, which are in turn crosscutby two-mica granite. This range in rock type is similar to therange displayed by Mesozoic granitoid suites found in the Cordilleraninterior of western North America. The lithological zones inthe White Creek batholith correlate with distinet jumps in majorelement, trace element, and isotopic compositions, and indicatethat several pulses of magma were emplaced within the WhiteCreek magma chamber. The hornblende-and biotite-bearing granitoidsare metaluminous to weakly peraluminous, have strong light rareearth element (LREE) enrichment, and small negative Eu anomalies.These granitoids have initial _Sr ranging from +32 to +84 (⁸⁷Sr/⁸⁶SrTfrom 0.7069 to 0.7106), initial _Nd ranging from –5 to–10, and initial ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pbranging from 18.3 to 18.7, 15.58 to 15.65, and 38.3 to 39.0,respectively. The two-mica granites and associated aplites arestrongly peraluminous, and show only moderate LREE enrichmentand strong negative Eu anomalies. These granites have _Sr rangingfrom +174 to + 436 (⁸⁷Sr/⁸⁶Sr_T from 0.7169 to 0.7354), _Nd rangingfrom –12 to –16, and more radiogenic initial Pbisotope ratios than the hornblende-and biotite-bearing granitoids. Oxygen, Sr, Pb, and Nd isotopes, REE modelling, and phase equilibriumconstraints are consistent with crustal anatexis of Precambrianbasement gneisses and Proterozoic metapelites exposed in southeastBritish Columbia, the product being the hornblende-biotite granitoidsand two-mica granites, respectively. The sequence of intrusionin the White Creek batholith constrains the melting sequence.A zone of anatexis proceeded upwards through the crust, firstmelting basement gneisses then melting overlying metapelites.A model for basaltic magmatic underplating as a primary causeof anatexis of the crust during the mid-Cretaceous magmaticepisode is difficult to reconcile with the absence of earlyCretaceous basalt in the southern Canadian Cordillera. A muchmore likely petrogenetic model is that crustal anatexis wasprobably a response to crustal thickening in association withterrane accretion and collision along the western margin ofthe North American continent.     

The shoshonite porphyry Cu-Au association in the Goonumbla District,N.S.W., Australia

Summary The Goonumbla porphyry copper-gold deposit in N.S.W., Australia, is hosted by late Ordovician (439.2 ± 1.2 Ma)shoshonitic igneous rocks. In terms of their petrography, the rocks vary from andesitic to dacitic lavas and tuffs which are partly intruded by monzonite stocks; they are characterized by high and variable Al₂O₃ (13.4–19.9 wt%), very high K₂O values (up to 6.8 wt%), and high K₂O/Na₂O ratios (0.58–1.48), which are typical for the shoshonite association. The rocks also have enriched LILE concentrations (Ba up to 1200 ppm, Sr up to 1350 ppm), low HFSE (TiO₂ < 0.67 wt%, Zr < 125 ppm, Nb < 10 ppm, Hf < 3.4 ppm), and very low LREE (La < 22.4 ppm, Ce < 31 ppm), which are typical for potassic volcanic rocks formed in alate oceanic-arc setting.Mineral chemistry of selected magmatic mica and apatite phenocrysts from host rocks reveals relatively high SrO and BaO contents (micas: 0.15 wt% and up to 0.28 wt%, respectively; apatites: up to 0.28 wt% and 0.19 wt%, respectively) and very high halogen concentrations. Micas are characterized by up to 3.9 wt% F and 0.14 wt% Cl, whereas apatites have up to 3.6 wt% F and 0.68 wt% Cl. These very high halogen contents compared to those from barren intrusions imply that the shoshonitic magmatism was the source of mineralization.Copper-gold mineralization consists mainly of bornite, chalcopyrite, chalcocite and minor pyrite and tetrahedrite. Native gold occurs mainly as minute grains within silicates of the host rocks, and more rarely as fine inclusions in the sulphides. Mineralization is accompanied by wallrock alteration comprising a spatially restricted potassic type and a regional propylitic alteration type.Thus, the porphyry copper-gold deposit in the Goonumbla district can be viewed as an additional example of a worldwide association between potassic/shoshonitic magmatism and base- and precious-metal mineralization. More specifically, it appears to be the oldest recorded example of a shoshontie-associated porphyry Cu-Au deposit from a late oceanic-arc setting, a possible modern analogue being Ladolam at Lihir Island, Papua New Guinea

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Die Shoshonit Porphyry Cu-Au Assoziation im Goonumbla Distrikt, N.S.W., Australien

Zusammenfassung Die Porphyry Cu-Au Vererzung im Goonumbla Distrikt in New South Wales, Australien, sitzt in oberordovizischen (ca. 439.2 ± 1.2 Ma) Shoshoniten auf. Das petrographische Spektrum dieser Gesteine reicht von andesitischen bis dazitischen Laven und Tuffen, die lokal von Monzonit-Stöcken intrudiert werden; die Gesteine besitzen hohe, aber variable Al₂O₃ Gehalte (13.4–19.9 Gew%), sehr hohe K₂O Gehalte (bis zu 6.8 Gew%) und hohe K₂O/Na₂O Verhältnisse (0.58–1.48), die typisch sind für Shoshonite. Außerdem weisen sie hohe Konzentrationen an LILE Elementen (Ba bis 1200 ppm, Sr bis 1350 ppm) auf und geringe Konzentrationen an HFSE (TiO₂ < 0.67 Gew%, Zr < 125 ppm, Nb < 10 ppm, Hf < 3.4 ppm) sowie an LREE (La < 22.4 ppm, Ce < 31 ppm), die als typisch gelten für potassische Vulkanite von ozeanischen Plattengrenzen.Die Mineralchemie von repräsentativen Glimmer- und Apatit-Phänokristallen ist charakterisiert durch hohe SrO und BaO Gehalte (Glimmer: 0.15 Gew%, bzw. bis 0.28 Gew%; Apatite: bis 0.28 Gew%, bzw. 0.19 Gew%). Sie enthalten ferner sehr hohe Halogen-Konzentrationen. Die Glimmer enthalten beispielsweise bis zu 3.9 Gew% F und 0.14 Gew% Cl, während Apatite bis zu 3.6 Gew% F und 0.68 Gew% Ci aufweisen. Dies erscheint nicht ungewöhnlich, weil Glimmer und Apatite von vererzten Mag matiten zumeist deutlich höhere Halogengehalte besitzen, als solche von unvererzten Magmatiten. Die hohen Halogen-Gehalte in Phänokristallen aus den Shoshoniten legen nahe, die Vulkanite als den Ursprung der Vererzung zu interpretieren.Die Cu-Au Vererzung besteht überwiegend aus den Sulfiden Bornit, Kupferkies, Kupferglanz und vereinzelt auftretendem Pyrit und Tetrahedrit. Gediegen Gold wird in der Regel nur als kleine Partikel innerhalb von Silikaten der shoshonitischen Wirtsgesteine und seltener als feine Einschlüsse in Sulfiden gefunden.Die Vererzung wird von hydrothermaler Alteration der Wirtsgesteine begleitet und zwei Alterationsarten lassen sich unterscheiden: eine potassische sowie eine regional zu beobachtende propylitische Alteration.Die Porphyry Cu-Au Lagerstätte im Goonumbla Gebiet ist ein Beispiel für die weltweit beobachtete Assoziation von Bunt- und Edelmetallvererzungen und potassisch/shoshonitischem Magmatismus. Der Goonumbla Distrikt stellt die älteste bisher bekannte Porphyry Cu-Au Lagerstätte aus einerspätgenetischen ozeanischen Plattengrenze dar. Einmodernes Beispiel für eine Cu-Au Lagerstätte vergleichbaren Typs ist Ladolam auf Lihir Island, Papua New Guinea.

     

The mesothermal gold-lamprophyre association: significance for an accretionary geodynamic setting,supercontinent cycles,and metallogenic processes

Summary Archean shoshonitic lamprophyres are cotemporal and cospatial with gold mineralization in the Superior Province of Canada, both being emplaced along translithospheric structures that demark subprovince boundaries. By analogy with geochemically similar Phanerozoic counterparts, the dikes are a product of specific plate interactions rather than a deep asthenosphere plume-initiated event, and their onset in the late-Archean at 2.7 Ga signifies that Phanerozoic style plate-tectonics was operating at this time. Fresh shonshonitic dikes are characterized by normal background gold contents of 3.9 ± 8.1 ppb (l), close to the value of 3.0 ppb for the bulk continental crust, and average abundances of As, Sb, Bi, W, TI, B, Cu, Pb, Zn, and Mo are also close to their values in bulk continental crust. Thus, fresh lamprophyres are not intrinsically enriched either in Au or elements affiliated with gold in mesothermal deposits, and accordingly do not constitute a special source rock. Platinum group element contents (Ir = 0.4 ± 0.58 ppb; Pt = 5.9 ± 26.5, Pd = 5.5 ± 1.8), in conjunction with Cu, Au, and Ni abundances, define approximately flat patterns on primitive mantle-normalized diagrams, consistent with derivation of the alkaline magmas from a depleted mantle source variably enriched by incompatible elements. Comparable abundances and ratios of Pd/Au, Os/Ir, and Ru/Ir in Archean lamprophyres, Archean komatiites, and Gorgona komatiites signify that the Archean and Phanerozoic upper mantle had similar noble metal contents, such that the prolific greenstone belt Au-Ag vein deposits cannot be explained by secular variations in upper mantle Au abundance alone. The lack of covariation between Au and light rare earth elements in lamprophyres rules out mantle metasomatism as a process generating intrinsically Au-rich magmas.Emplacement of the lamprophyres was diachronous from north (2710 Ma) to south (2670 Ma) in the Superior Province, as was the gold mineralization. Both were related to late transpressional tectonics during successive accretions of individual subprovinces. Alkaline magmatism and gold mineralization are temporally and spatially related because they share a common geodynamic setting, but they are otherwise the products of distinct processes. Much of Archean time was devoid of shoshonites and mesothermal gold deposits. The first widespread inception of this duality at 2.71–2.65 Ga in the Superior and Slave Provinces, Canada, and in India and Australia, may reflect one of the first supercontinent aggregations involving accretionary, Cordilleran style tectonics. Giant mesothermal gold provinces and shoshonites recur through time in the Palaeozoic and Mesozoic in this geodynamic setting.

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Die mesothermale Gold-Lamprophyrassoziation und ihre Bedeutung für Akkretionsgeotektonik, Superkontinent-Zyklen und metallogenetische Prozesse

Zusammenfassung Archaische schoschonitische Lamprophyre sind zeitlich und räumich mit Goldmineralisationen in der Superior Provinz Kanadas vergesellschaftet; beide sind an translithosphärische Strukturen, die die Grenzen von Subprovinzen markieren, geknüpft. Ein Vergleich mit geochemisch ähnlichen phanerozoischen Abfolgen weist darauf hin, daß die Gänge eher durch spezifische Platteninteraktions- und nicht durch Hot Spot initiierte asthenosphärische Prozesse entstanden sind. Ihre spät-archaische Alterseinstufung (ca. 2.7 Ga) belegt somit, daß bereits zu dieser Zeit plattentektonische Prozesse, wie sie für das Phanerozoikum typisch sind, funktionierten.Frische schoschonitische Gänge zeigen mit Durchschnittskruste vergleichbare Untergrundgehalte an Gold von 3.9 ± 8.1 ppb (l), Auch die Gehalte an As, Sb, Bi, W, Tl, B, Cu, Pb, Zn und Mo entsprechen Gehalten der durchschnittlichen Erdkruste. Frische Lamprophyre sind daher nicht an Gold bzw. an anderen für mesothermale AuLagerstätten typischen Elementen angereichert und stellen somit keine spezifischen Muttergesteine dar. Die Gehalte an Platingruppen-Elementen (Ir = 0.4 ± 0.58 ppb; Pt = 5.9 ± 26.5; Pd 5.5 ± 1.8) in Verbindung mit der Verteilung von Cu, Au und Ni definieren einen flachen Trend in auf primitiven Mantel normierten Diagrammen, was mit einer Herkunft der alkalischem Magmen aus einer abgereicherten Mantelquelle, die im unterschiedlichen Ausmaß an einzelnen inkompatiblen Elementen angereichert ist, hinweist. Ähnliche Elementverteilungen bzw. verhältnisse von Pd/Au, Os/Ir und Ru/Ir in archaischen Lamprophyren, archaischen Komatiiten und Gorgona-Komatiiten belegen, daß der archaische und phanerozoische obere Mantel ähnliche Gehalte an Edelund Buntmetallen aufweisen. Die Au-Ag Ganglagerstätten in Greenstone Belts können daher nicht ausschließlich mit einer Variation der Au-Gehalte des oberen Erdmantels erklärt werden. Die fehlende Korrelation zwischen Au und den leichten Seltenen Erden in den Lamprophyren schließt mantelmetasomatische Prozesse für die Bildung von Au-reichen Magmen aus.Die Platznahme der Lamprophyre in der Superior Provinz erfolgte zeitgleich von N (2710 Ma) nach S (2670 Ma) mit der Bildung der Goldmineralisationen. Beide stehen mit einer späten transpressionalen Tektonik während der sukzessiven Akkretion einzelner Subprovinzen in Beziehung. Alkalimagmatismus und Goldmineralisationen sind deshalb räumlich und zeitlich vergesellschaftet, weil sie innerhalb desselben geodynamischen Settings gebildet wurden. Sie sind sonst aber Produkte unterschiedlicher Prozesse. Über weite Zeiträume des Archaikums fehlen Schoschonite und mesothermale Goldlagerstätten. Das erste großangelgte Auftreten beider in der Superior und Slave Provinz Kanadas während 2.71-2.65 Ga und in Indien und Australien könnte eine der ersten Superkontinentaggregationen im Stile einer Cordillera-style Akkretionstektonik widerspiegeln. Riesige mesothermale Goldprovinzen und Schoschonite treten während des Paläo- und Mesozoikums immer wieder, gebunden an diese geotektonische Position, in Erscheinung.

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With 7 Figures     

Geochemistry and origin of the Proterozoic ultrapotassic rocks of the Churchill Province,Canada

Summary Early Proterozoic ultrapotassic dikes, lava flows, and pyroclastic rocks of the Christopher Island Formation (CIF) erupted throughout an area 600 × 300 km within the Churchill Province of the Canadian Shield at 1.84 Ga. The rocks range from mafic lamprophyres (mg # 60; SiO₂ 47–54%, mean K₂O/Na₂O > 4) with phenocrysts of phlogopite + diopside + apatite ± olivine ± magnetite, to phenocryst-poor felsic rocks and sanidine porphyries (SiO₂55–69%). All samples have high incompatible element contents and display large depletions of high field strength elements relative to K, Rb, Sr, Ba, and Th. The CIF has geochemical and petrographic characteristics of both minettes and lamproites, but overall most closely resembles young Mediterranean lamproites. Felsic rocks of the CIF were produced by crystal fractionation and crustal contamination of mafic ultrapotassic magma, and include both high-silica lamproites strongly enriched in Zr, U, and Th, and weakly potassic to sodic rocks of trachytic composition. Flows and feeder dikes have relatively homogeneous _{Nd, 1840 Ma} (–6 to –11) but highly variable ES., 1840 Ma (–40 to + 100); samples classified as lamproites have higher average _Sr. Dike samples have highly variable present-day Pb isotope compositions, ranging from moderately to strongly nonradiogenic. Geochemical and isotopic data are consistent with contributions from depleted Archean lithospheric mantle, and OIB-type convecting mantle, both metasomatized by subduction-related processes during the Early Proterozoic. The lithospheric mantle probably contained Archean enriched domains as well. Proterozoic enrichment may have accompanied shallow underplating of subducted oceanic lithosphere beneath the Churchill Province during amalgamation of the Laurentian supercontinent. There are strong analogies in isotopic composition, and interpreted source region history, between the CIF and lamproites and minettes of the Wyoming Province and western Greenland, which suggest the existence of a Laurentian ultrapotassic superprovince.

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Geochemie und Entstehung der Proterozoischen ultrapotassischen Gesteine der Churchill Provinz, Kanada

Zusammenfassung Altproterozoische, ultrapotassische Gänge, Lavaströme und pyroklastische Gesteine der Christopher Island Formation (CIF), eruptierten in einem Gebiet von 600 × 300 km in der Churchill Provinz des Kanadischen Schildes vor 1.84 Ga. Die Zusammensetzung dieser Gesteine variiert von mafischen Lamprophyren (mg > 60; SiO₂ = 47–54%, durchschnittliches K₂O/Na₂O > 4) mit Phänokristallent von Phlogopit + Diopsid + Apatit + Olivin + Magnetit, bis zu phänokristallarmen felsischen Gesteinen und Sanidinporphyren (SiO₂ = 55–69%). Alle Proben zeigen hohe Gehalte an inkompatiblen Elementen und zeigen beträchtliche Verarmung an high field strength Elementen relativ zu K, Rb, Sr, Ba und Th. Die CIF hat geochemische und petrographische Eigenschaften sowohl von Minetten wie von Lamproiten, aber im allgemeinen ähnelt sie am stärksten jungen mediterranen Lamproiten. Felsische Gesteine der CIF wurden durch Fraktionierung und Krustenkontamination aus mafischen ultrapotassischen Magmen gebildet. Letztere umfassen sowohl siliziumreiche Lamproite, die deutlich an Zr, U und Th angereichert sind und schwach potassische bis sodische Gesteine von trachytischer Zusammensetzung. Lavenergüsse und zufuhrgänge zeigent ein relativ homogenes _{Nd, 1840 Ma} (–6 bis –11) aber ein sehr variables _{Sr, 1840 Ma} (-40 bis + 100); Proben die als Lamproite klassifiziert wurden, zeigent höhere durchschnittliche _Sr-Werte. Proben von Gängen haben sehr variable Bleiisotopen-Zusammensetzungen, die von mäßig bis stark nichtradiogen variieren. Geochemische und Isotopendaten weisen auf Beiträge aus verarmtem archaischen lithosphärischen Mantel und aus konvektierendem OIB-Typ Mantel hin, die beide während des Alproterozoikums durch Subduktions-Vorgänge metasomatisiert wurden. Der lithosphärische Mantel enthielt wahrscheinlich auch angereicherte archaische Domänen. Proterozoische Anreicherungsvorgänge dürften seichtes Underplating subduzierter ozeanischer Lithosphäre unter der Churchill Provinz während der Amalgamation des laurentischen Superkontinentes begleitet haben. Es gibt starke Analogien in der Isotopenzusammensetzung und in der interpretierten Geschichte der Ursprungsregion, zwischen den CIF und Lamproiten und Minetten der Wyoming Provinz, und des westlichen Grönland. Diese weisen auf die Existenz einer laurentischen ultrapotassischen Superprovinz hin.

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Dike rock generation and magma interactions in the Bir Safsaf igneous complex,south-west Egypt: Implications for the Pan-African evolution in north-east Africa

The geological setting, ages, petrography and geochemistry of late Pan-African ( 580 Ma) calc-alkaline and tholeiitic dike rocks in the Bir Safsaf igneous complex of south-west Egypt are discussed. These basaltic to rhyolitic dikes intruded contemporaneously and shortly after the intrusion of granitoids. The major and trace element data, Sr and Nd isotope relations, in combination with textural observations, confirm complex interactions between most of the intermediate calcalkaline dike melts and plutonic melts, with different degrees of mixing, assimilation, replenishment and tapping of magma chambers. Trachytic and rhyolitic dikes are strongly differentiated melts from the granitic pluton. The tholeiitic dikes evolved dominantly by fractional crystallization processes. It is inferred that open system and closed system processes operated in calc-alkaline magma chambers, and that the calc-alkaline melts came from a garnet-and amphibole-bearing mantle, modified by a subduction component. Tholeiitic rocks were formed later by fractional crystallization and assimilation processes. Magma ascent of both dike types took place in an extensional environment and the presumed subduction zone has to be seen in connection with the Atmur-Delgo suture zone.