Showing papers in "Contributions to Mineralogy and Petrology in 1986"

Trace element characteristics of graywackes and tectonic setting discrimination of sedimentary basins

Abstract: The graywackes of Paleozoic turbidite sequences of eastern Australia show a large variation in their trace element characteristics, which reflect distinct provenance types and tectonic settings for various suites. The tectonic settings recognised are oceanic island arc, continental island arc, active continental margin, and passive margins. Immobile trace elements, e.g. La, Ce, Nd, Th, Zr, Nb, Y, Sc and Co are very useful in tectonic setting discrimination. In general, there is a systematic increase in light rare earth elements (La, Ce, Nd), Th, Nb and the Ba/Sr, Rb/Sr, La/Y and Ni/Co ratios and a decrease in V, Sc and the Ba/Rb, K/Th and K/U ratios in graywackes from oceanic island arc to continental island arc to active continental margin to passive margin settings. On the basis of graywacke geochemistry, the optimum discrimination of the tectonic settings of sedimentary basins is achieved by La-Th, La-Th-Sc, Ti/Zr-La/Sc, La/Y-Sc/Cr, Th-Sc-Zr/10 and Th-Co-Zr/10 plots. The analysed oceanic island arc graywackes are characterised by extremely low abundances of La, Th, U, Zr, Nb; low Th/U and high La/Sc, La/Th, Ti/Zr, Zr/Th ratios. The studied graywackes of the continental island arc type setting are characterised by increased abundances of La, Th, U, Zr and Nb, and can be identified by the La-Th-Sc and La/Sc versus Ti/Zr plots. Active continental margin and passive margin graywackes are discriminated by the Th-Sc-Zr/10 and Th-Co-Zr/10 plots and associated parameters (e.g. Th/Zr, Th/Sc). The most important characteristic of the analysed passive margin type graywackes is the increased abundance of Zr, high Zr/Th and lower Ba, Rb, Sr and Ti/Zr ratio compared to the active continental margin graywackes.

Confined fission track lengths in apatite: a diagnostic tool for thermal history analysis

Abstract: Fission-track ages in apatite are generally accepted as giving a measure of the time over which a sample has been exposed to temperatures below approximately 100° C. A compilation of the lengths of confined fission tracks in a wide variety of apatites from different geological environments has shown that the distribution of confined track lengths can provide unique thermal history information in the temperature range below about 150° C over times of the order of 106 to 109 years. The distribution of confined lengths of freshly produced induced tracks is characterised by a narrow, symmetrical distribution with a mean length of around 16.3 μm and a standard deviation of the distribution of approximately 0.9 μm. In volcanic and related rocks which have cooled very rapidly, and never been reheated above about 50° C, the distribution is also narrow and symmetric, but with a shorter mean of 14.5 to 15 μm, and a standard deviation of the distribution of approximately 1.0 μm. In granitic basement terrains which are thought never to have been significantly disturbed thermally, since their original post-emplacement cooling, the distribution becomes negatively skewed, with a mean around 12 or 13 μm and a standard deviation between 1.2 and 2 μm.This distribution is thought to characterise slow continuous cooling from temperatures in excess of 120° C, to ambient surface temperatures. More complex thermal histories produce correspondingly complex distributions of confined tracks. The continuous production of tracks through time, coupled with the fact that the length of each track shrinks to a value characteristic of the maximum temperature it has experienced, gives a final length distribution which directly reflects the nature of the variation of temperature with time. Most distinctive of the myriad possible forms of the final distribution are the bimodal distributions, which give clear evidence of a two-stage history, including high and low temperature phases. The study of confined length distributions therefore offers invaluable evidence on the meaning of any fission-track age, and bears the potential of providing rigorous constraints on thermal history in the temperature regime below about 150° C. The results of this study strongly suggest that any apatite fission-track age determination should be supported by a confined track length distribution.

Cooling and uplift patterns in the Lepontine Alps South Central Switzerland and an age of vertical movement on the Insubric fault line

Abstract: 96 new fission track (FT) apatite and zircon, K/Ar and Rb/Sr biotite and muscovite ages are presented for 19 samples (mainly acid gneisses) from a 40 km traverse through the Lepontine Alps in the Maggia Valley, South Central Switzerland. Plotting measured mineral ages against assumed system closure temperatures yields cooling rates for each sample. The entire profile shows a fairly uniform Late Neogene-Recent mean uplift rate of ∼0.5 mm/a, confirmed by a gradient of FT apatite age with elevation. Cooling from higher temperatures occurred earlier in the south, where uplift rates of ∼2.2 mm/a in the Steep Belt (root zone) indicate >9 km Early Miocene uplift of the northern Pennine block. This uplift started before 23 Ma and is interpreted as resulting from a major phase of backthrusting along the Insubric Line, and as dating the formation of the mylonite belt. Estimated cooling rates constrain the timing of Lepontine Mid-Tertiary metamorphism: 3 schematic models are proposed which also consider published Rb/Sr, K/Ar mica and hornblende and U/Pb monazite ages. Slow cooling, differential initial heating and subsequent cooling of different parts of the Central Alps and post-38 Ma cooling with syntectonic metamorphism at ∼27 Ma are postulated as alternative interpretations of isotopic data and geologic evidence. From extrapolation between K/Ar and Rb/Sr mica ages and apatite FT ages, 240±50° C is proposed as the closure temperature for the retention of fission tracks in zircon.

Whole-grain evaporation for 207Pb/206Pb-age-investigations on single zircons using a double-filament thermal ion source

Abstract: A technique has been developed and tested to analyse 207Pb/206Pb apparent ages by thermal evaporation of radiogenic lead directly from untreated whole zircon grains (≤0.3 mm). The evaporation analyses are performed in the double-filament arrangement of a thermal ion mass spectrometer (ThIMS). The method is a powerful tool to distinguish between different lead components occurring in the same grain because differing activation energies of the competing lead components cause their sequential evaporation from the zircons. The evaporation of test samples results in 207Pb/206Pb apparent ages in good agreement with U/Pb ages known from literature: single zircons from a granite of the ‘Marble Mountains’/California yield an age of crystallization of 1,410±30 Ma; ‘Ceylon’ zircons from heavy-mineral bearing gravels yield 560± 40 Ma as age of crystallization of the pegmatitic gravel sources; individuals from a heterogeneous zircon population of a diatexite from the Southern Schwarzwald/SW-Germany indicate metamorphic zircon formation around 500 Ma and the existence of Middle-Proterozoic relics (1.95±0.05 Ga).

Partition coefficients of Hf, Zr, and REE between zircon, apatite, and liquid

Abstract: Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10–100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite.

Monazite solubility and dissolution kinetics: implications for the thorium and light rare earth chemistry of felsic magmas

Abstract: A series of monazite dissolution experiments was conducted in a hydrous (1–6 wt%) granitic melt at 8 kbar over the temperature range 1,000–1,400° C A polished cube of monazite was immersed in a natural obsidian melt and allowed to partially dissolve Electron microprobe traverses perpendicular to the crystal-melt interface revealed concentration gradients in the LREEs and P Diffusivities of the LREEs and P were calculated from these profiles, yielding the following Arrhenius relations for the LREEs: D=023 exp(−601 kcal mol−1/RT) at 6% water D=230×107 exp(−1221 kcal mol−1/RT) at 1% water These results demonstrate the importance of dissolved water on REE diffusion Phosphorus diffusivities are nearly identical to those of the rare-earths, suggesting that P diffusion charge-compensates REE diffusion The concentration of LREEs required for monazite saturation in these melts is given by the level of dissolved LREEs at the crystal-melt interface These values also show a dependence on dissolved water, with LREEsat=60 ppm at 6% H2O when extrapolated down to 700° C, and LREEsat=30 ppm at 1% H2O Calculated dissolution rates based on the above parameters indicate that minute ( 2% H2O), whereas larger (> 50 μm) crystals will likely be residual over the duration of an anatectic event The low solubility of monazite in this melt suggests that the LREE depletion observed in some felsic differentiation suites may be the result of monazite crystallization Limited experimental and geochemical/petrologic evidence indicates that compositional changes in the melt accompanying differentiation decrease the solubility of monazite drastically Kinetic and chemical constraints may also lead to localized monazite saturation and inclusion in major phases or even other accessories Variations in the REE composition of monazite from different parageneses probably reflects the REE pattern of the parent melt, and may be due to gradational differences in the stability of individual or subgroup REE-complexes as a function of melt composition Particularly important in this regard seems to be the lime+alkali/alumina balance of the melt and its volatile content

The effect of trapped liquid crystallization on cumulus mineral compositions in layered intrusions

Abstract: A series of calculations have been carried out to evaluate the effect on cumulus mineral compositions of solidification of trapped intercumulus liquid in orthocumulates. The calculation assumes local equilibrium between phases, and that the system remains chemically closed during crystallization of the trapped liquid. The latter assumption is held to be valid on a scale of tens to hundreds of centimeters. It is not necessary to know the composition of the trapped liquid, as the calculation only requires an estimate of FeO content and trapping temperature. The change in composition of a mineral from that of the initially precipitated cumulus crystals to the final composition after complete solidification is termed the “trapped liquid shift”. Its magnitude depends on the modal proportions of cumulus phases and the initial porosity, and is only weakly dependent on initial phase compositions. Trapped liquid shifts are significant when compared with mineral composition changes occurring during fractional crystallization. Crystallization of 30% trapped liquid gives rise to shifts of up to 10 mol. percent in Mg number of olivine or pyroxene. The size of the shift becomes greater when the initial cumulus assemblage has a lower total FeO+MgO content, and vice versa. As a result of the relationship between trapped liquid shift and cumulus mode, mineral composition variations and trends may be generated in sequences of cumulates which originally had constant compositions of cumulus minerals. For example, in a cyclic unit grading from a pyroxenitic base to an anorthositic top, crystallization of a uniform proportion of trapped liquid will result in an apparent iron enrichment trend from bottom to top of the cycle, as has been observed in the Upper Critical Zone of the Bushveld Complex.

40 Ar/ 39 Ar dating of white micas from an Alpine high-pressure metamorphic belt on Naxos (Greece): the resetting of the argon isotopic system

Abstract: Overprinting of white micas from high pressure, low to medium temperature (M 1) metamorphic assemblages in pelitic schists on Naxos during subsequent thermal dome (M 2) metamorphism ranges from minor in the southeast of the island to complete recrystallization in the amphibolite facies rocks near the migmatites in the centre of the dome. The original (M 1) minerals are phengites (Si4+=6.7–7.0) and the overprinting minerals are muscovites (Si4+=6.0–6.45). 40Ar/39Ar step heating analyses of white mica separates from rocks in the area where phengite and muscovite occur together yield complex age spectra, characterized by low apparent ages in the first and the last stages of gas release and high apparent ages in between. These upward-convex age spectra are shown to be caused by mixing of two generations of micas, each of which has a different age spectrum and argon release pattern. Seemingly good plateaus in some age spectra from white micas of the area must be interpreted as providing meaningless intermediate ages. Further, the upward-convex age spectra have been used to trace the isotopic signature of phengites toward increasing M 2 metamorphic grade, and suggest that as long as phengites can be observed in the rocks upward-convex age spectra occur. On Naxos, crystallization of muscovite at the expense of phengite appears to be the main mechanism of resetting argon isotopic ages in white micas. However, there is also good evidence for argon loss by volume diffusion from phengites. Simple diffusion calculations suggest that the M 2 metamorphism was caused by a shortlived heat source.

The evolution of illite to muscovite; mineralogical and isotopic data from the Glarus Alps, Switzerland

Abstract: Thirty-five illite and muscovite concentrates were extracted from Triassic and Permian claystones, shales, slates and phyllites along a cross-section from the diagenetic Alpine foreland (Tabular Jura and borehole samples beneath the Molasse Basin) to the anchi- and epimetamorphic Helvetic Zone of the Central Alps. Concentrates and thin sections were investigated by microscopic, X-ray, infrared, Mossbauer, thermal (DTA and TG), wet chemical, electron microprobe, K-Ar, Rb-Sr, 40Ar/39Ar and stable isotope methods. With increasing metamorphic grade based on illite “crystallinity” data (XRD and IR) the following continuous changes are observed: (i) the 1Md→2M1 polymorph transformation is completed in the higher grade anchizone; (ii) K2O increases from 6–8 wt. % (diagenetic zone) to 8.5–10% (anchizone) to 10–11.5% (epizone), reflecting an increase in the total negative layer charge from 1.2 to 2.0; (iii) a decrease of the chemical variation of the mica population with detrital muscovite surviving up to the anchizone/ epizone boundary; iv) a shift of an endothermic peak in differential thermal curves from 500 to 750° C; (v) K-Ar and Rb-Sr apparent ages of the fraction <2 μm decrease from the diagenetic zone to the epizone, K-Ar ages being generally lower than Rb-Sr ages. The critical temperature for total Ar resetting is estimated to be 260±30° C. K-Ar and Rb-Sr ages become concordant when the anchizone/ epizone boundary is approached. The stable isotope data, on the other hand, show no change with metamorphic grade but are dependent on stratigraphic age. These results suggest that the prograde evolution from 1 Md illite to 2M1 muscovite involves a continuous lattice restructuration without rupture of the tetrahedral and octahedral bonds and change of the hydroxyl radicals, however this is not a recrystallization process. This restructuration is completed approximately at the anchizone/epizone boundary. The isotopic data indicate significant diffusive loss of 40Ar and 87Sr prior to any observable lattice reorganization. The restructuration progressively introduces a consistent repartition of Ar and K in the mineral lattices and is outlined by the 40Ar/39Ar age spectra. Concordant K-Ar and Rb-Sr ages of around 35-30 Ma. with concomitant concordant 40Ar/39Ar release spectra are representative for the main phase of Alpine metamorphism (Calanda phase) in the Glarus Alps. A second age group between 25 and 20 Ma. can probably be attributed to movements along the Glarus thrust (Ruchi phase), while values down to 9 Ma., in regions with higher metamorphic conditions, suggest thermal conditions persisting at least until the middle Tortonian.

The evolution of young silicic lavas at Medicine Lake Volcano, California: Implications for the origin of compositional gaps in calc-alkaline series lavas

Abstract: At Medicine Lake Volcano, California, the compositional gap between andesite (57–62 wt.% SiO2) and rhyolite (73–74 wt.% SiO2) has been generated by fractional crystallization. Assimilation of silicic crust has also occurred along with fractionation. Two varieties of inclusions found in Holocene rhyolite flows, hornblende gabbros and aphyric andesites, provide information on the crystallization path followed by lavas parental to the rhyolite. The hornblende gabbros are magmatic cumulate residues and their mineral assemblages are preserved evidence of the phases that crystallized from an andesitic precursor lava to generate the rhyolite lavas. The andesitic inclusions represent samples of a parental andesite and record the early part of the differentiation history. Olivine, plagioclase and augite crystallization begins the differentiation history, followed by the disappearance of olivine and augite through reaction with the liquid to form orthopyroxene and amphibole. Further crystallization of the assemblage plagioclase, amphibole, orthopyroxene, magnetite, and apatite from a high-SiO2 andesite leads to rhyolite. This final crystallization process occurs on a cotectic that is nearly horizontal in temperature-composition space. Since a large amount of crystallization occurs over a limited temperature interval, a compositional gap develops between rhyolite and high SiO2 andesite. Liquidus surfaces with shallow slopes in temperature-composition space are characteristic of several late-stage crystallization assemblages in the andesite to rhyolite compositional range. Experimentally produced plagioclase+ amphibole+orthopyroxene+magnetite and plagioclase+ augite+low-Ca pyroxene+magnetite cotectics have liquidus slopes that are nearly flat. At other calc-alkaline volcanic centers crystallization processes involving large compositional changes over small temperature intervals may also be important in the development of bimodal volcanism (i.e. the existence of a composition gap). At Mt. Mazama and Mt. St. Helens, USA and Aso Caldera and Shikotsu, Japan the amphibole-bearing assemblage was important. At Krakatau, Indonesia and Katmai, USA, an augite+orthopyroxene-bearing assemblage was important. In addition to its role in the production of a compositional gap between intermediate and rhyolitic lavas, the crystallization process increases the H2O content of the residual liquid. This rapid increase in residual liquid volatile content which results from the precipitation of a large proportion of crystalline solids may be an important factor among several that lead to explosive silicic eruptions.

Four zircon ages from one rock: the history of a 3930 Ma-old granulite from Mount Sones, Enderby Land, Antarctica

Abstract: Ion microprobe U-Th-Pb analyses of zircons from a granulite-grade orthogneiss from Mount Sones, Enderby Land, Antarctica, record the ages of four principal events in the history of the gneiss, three of which already have been recognized through previous isotopic dating of other samples. The structure of the zircons indicates at least four different stages of growth. The several zircon ages were obtained by grouping the analyses according to the stage they represented in the observed “stratigraphic succession” of growth and thereby defining separate U-Pb discordance patterns for each stage. The stratigraphically oldest zircon (rare discrete cores) is indistinguishable in age from the most common, euhedrally zoned zircon. Both crystallized when the tonalitic precursor of the orthogneiss was emplaced into the crust 3927±10 Ma ago, making the orthogneiss currently the oldest known terrestrial rock. The outer parts of most grains and some whole grains recrystallized at 2948±31/−17 Ma, during or immediately after possibly ∼100 Ma of high granulite grade metamorphism. The recrystallized zircon was isotopically disturbed by tectonism associated with reactivation of the southern margin of the Napier Complex at ∼1000 Ma. In the intervening time, at 2479±23 Ma, the cores and zoned zircon suffered a major isotopic disturbance involving movement of radiogenic Pb which left most of the crystals with radiogenic Pb deficiencies, but produced local radiogenic Pb excesses in others. A new generation of zircon, characterized by very high Th/U and low U, grew at that time. That event — deformation and possibly a minor rise in temperature — produced widespread perturbations of other isotopic systems throughout the Napier Complex.

Sulfide and platinum mineralization in the Merensky Reef: evidence from hydrous silicates and fluid inclusions

Abstract: The base metal sulfides of the Merensky Reef are associated with hydrous silicates and intense deuteric hydrous alteration of cumulus and postcumulus silicates. Biotite and phlogopite crystallized in the vicinity of sulfides from a volatile-enriched highly fractionated intercumulus melt. Amphibole, chlorite, and talc are later alteration phases of cumulus pyroxene and intercumulus plagioclase. Biotite is often accompanied by zircon, rutile, and quartz. Accessory quartz hosts a complex suite of H2O-NaCl-(CaCl2)-CO2-CH4 fluid inclusions which have thus far not been described from the Merensky Reef. The earliest fluid inclusion compositions are NaCl-(H2O) with less than 10 vol.% water; CO2 coexisting with a halite daughter crystal and brine; and polyphase inclusions with up to six daughter and accidental phases and high contents of divalent cations. The maximum trapping temperature is around 730° C at 4 to 5 kb pressure. Later inclusion generations are H2O-NaCl, CO2-H2O, and pure CO2 and CH4. The presence of Cl-rich fluids during the intercumulus stage of the crystallizing Merensky Reef is directly related to the mode of sulfide precipitation. Prior to sulfide unmixing in a hydrous magma sulfur is likely to be present as H2S. Sulfur saturation causes reaction of H2S with oxides of the silicate melt to form a sulfide melt plus water. During reaction the magma is enriched in water until a separate fluid unmixes. It carries all compounds with high fluid/melt partition coefficients, as well as metals capable of forming OH- and Cl-complexes. Precious metals are assumed to have fractionated into the Cl-rich fluid as Cl-complexes rather than being dissolved in the sulfide melt. During the cooling evolution of the fluid the precious elements precipitate around the periphery of sulfide melt droplets. The model proposed explains the distribution pattern of platinum-group minerals in the Merensky Reef better than any orthomagmatic mineralization concept offered so far.

Origin of continental crust of 1.9-1.7 Ga age: Nd isotopes and U-Pb zircon ages in the Svecokarelian terrain of South Finland

Abstract: Initial Nd isotopic ratios are reported for 23 samples representing magmatic crustal components in the Svecokarelian terrain of South Finland. U-Pb zircon ages are determined for all geologic units, involving 21 separate upper concordia intercept ages based on more than 100 UP-b analyses. The ages range for all the rocks from 1.90 Ga for primitve plutonic rocks to 1.79 Ga for post-tectonic intrusions. The well-known gabbro-diorite-tonalite-trondhjemite association of the Kalanti district appears to consist of components with different ages: trondhjemites are probably 1.90 Ga or older, diorites/tonalites belong to the main Svecokarelian plutonic eposide at 1.89-1.87 Ga, and at least some gabbro has a post-tectonic age of 1.80 Ga. ɛ Nd (T) values range between +2 to +3 for meta-andesites, large gabbros and primitive granitoids to −0.5 for more evolved granitoids. A magma source with ɛ Nd of at least +2 to +3 was available during 1.90 to 1.87 Ga, but evolved granitoids have ɛ Nd close to zero. The preferred interpretation is that depleted mantle with ɛ Nd=+4 to +5 was present beneath the Svecokarelian crust forming during 1.9-1.8 Ga, and that all rocks have been affected more or less by addition of an Archean crustal component with ɛ Nd=−9 to −13. The primitive rocks with ɛ Nd=+2 to + 3 were only slightly affected, while granitoids with ɛ Nd close to zero include a ∼10% Archean component. The widespread nature of the Archean addition and the distance of up to 500 km to actual exposed Archean crust make it most realistic that the Archean component was added to the form of sediments delivered by subducting Proterozoic ocean crust. The plutonic rocks of the Finnish Svecokarelian crust in areas away from Archean cratons consist of ∼90% newly mantle-derived material.

Spinel-pyroxene-garnet relationships and their dependence on Cr/Al ratio

Abstract: The partitioning of Cr and Al between coexisting spinel and clinopyroxene and the dependence of spinel-cpxgarnet equilibria on Cr/Al ratio have been investigated by a combination of phase equilibrium experiments, high temperature solution calorimetry and thermodynamic calculations. The exchange equilibrium: $$\begin{gathered} {\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 {2 }}}\right.\kern- ulldelimiterspace}\!\lower0.7ex\hbox{${2 }$}}MgAl_2 O_4 + NaCrSi_2 O_6 = {\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 {2 }}}\right.\kern- ulldelimiterspace}\!\lower0.7ex\hbox{${2 }$}}MgCr_2 O_4 + NaAlSi_2 O_6 \hfill \\ spinel clinopyroxene spinel clinopyroxene \hfill \\ \end{gathered} $$ has a measured enthalpy change for pure phases of −2,100±500 cal at 970 K and 1 atm. Experimental reversals of Cr-Al partitioning between the spinel and clinopyroxene phases yield the following partitioning relationship: $$X$$ where X i j refers to atomic fraction of i in the octahedral sites of phase j. The compositional dependence of partitioning implies that Al-Cr mixing in spinel is nonideal with, on the symmetrical model, a W Cr-Al Sp of 2,700±500 cal/gm. atom. In contrast, aluminum-chromium mixing in clinopyroxene is close to ideal. The measured stability field of knorringite (Mg3Cr2Si2O12) and mixing properties of garnet have been used in conjunction with our experimental data to calculate the influence of Cr/Al ratio on the important reaction: orthopyroxene+clinopyroxene+spinel=olivine+garnet The stability field of spinel lherzolite increases by about 2.8 Kb for every increase of 0.1 in Cr/(Cr+Al) ratio up to Cr/(Cr+Al) of 0.7. The calculated stabilization is in very good agreement with the experimental results of O'Neill (1981). The partitioning relationships are such that, at the low ratios of Cr/Al (∼0.07) of primitive lherzolite, clinopyroxene buffers spinel composition and sharpens the spinelgarnet reaction interval from 10 Kb (little or no clinopyroxene) down to about 2 Kb in pyroxene-rich “pyrolite.”

Petrogenesis of a Late Precambrian (575–600 Ma) bimodal suite in Northeast Africa

Abstract: Late Precambrian crustal evolution in the North Eastern Desert of Egypt occurred in a strongly extensional tectonic environment and was accompanied by abundant bimodal igneous activity. The extrusive and intrusive expressions of this magmatism, known as the Dokhan Volcanics and Pink Granites, respectively, were studied in detail from two areas. The Dokhan Volcanics and associated feeder dikes consist of a “mafic” suite dominated by andesites (∼60% SiO2) and smaller volumes of basalt and a “felsic” suite composed of rhyolite tuffs, ignimbrites and hypabyssal intrusions (∼72–78% SiO2). The rocks of the mafic suite display calc-alkaline trends on an AFM diagram but are enriched in incompatibles such as TiO2, P2O5, K2O, Rb, Sr, Ba, Zr, Y, Nb, and LREE. Rare earth element patterns are steep, with (Ce/Yb)n = 7.7 to 16.8. They contain moderate Ni (60 ppm) and Cr (95 ppm), indicating limited low-P fractionation. The melts of the mafic suite are interpreted to have formed either by ≤25% batch melting of eclogite or by ∼10% batch melting of LREE-enriched garnet lherzolite. The rocks of the felsic suite include Dokhan rhyolites and the epizonal Pink Granites. These contain 72–78% SiO2, are metaluminous and peraluminous, and have the high K2O/Na2O and FeO*/(FeO*+MgO) characteristic of post-tectonic, “A-type” granites. They are moderately enriched in incompatible elements, but their REE patterns overlap with those of the mafic suite, from which they can be distinguished by deep europium anomalies (Eu/Eu*=0.08–0.64) and flat HREE patterns=((Yb/Er)n=0.90–1.16). They share with the rocks of the mafic suite isotopic characteristics of depleted mantle, precluding anatexis of much older continental crust. The europium anomalies covary with Sr contents and indicate that plagioclase control was important, while the flat HREE patterns preclude residual garnet in the source. Hence the felsic melts could not have formed by anatexis of garnet-bearing mafic lower crust. Such melts could have formed by anatexis of amphibolite-facies crust, an interpretation which is not favored because the melts are not saturated with P2O5. Alternatively, the felsic melts may have formed via low-P fractional crystallization of the mafic melts, with about 2/3 removal of mostly plagioclase and amphibole along with minor apatite and zircon. This may have been accompanied in the latest stages of magmatic evolution by liquid-state fractionation such as thermo-gravitational diffusion or halide complexing.

Isotopic variation in the Tuolumne Intrusive Suite, central Sierra Nevada, California

Abstract: Granitoid rocks of the compositionally zoned Late Cretaceous Toulumne Intrusive Suite in the central Sierra Nevada, California, have initial87Sr/86Sr values (Sri) and143Nd/144Nd values (Ndi) that vary from 0.7057 to 0.7067 and from 0.51239 to 0.51211 respectively. The observed variation of both Sri and Ndi and of chemical composition in rocks of the suite cannot be due to crystal fractionation of magma solely under closed system conditons. The largest variation in chemistry, Ndi, and Sri is present in the outer-most equigranular units of the Tuolumne Intrusive Suite. Sri varies positively with SiO2, Na2O, K2O, and Rb concentrations, and negatively with Ndi, Al2O3, Fe2O3, MgO, FeO, CaO, MnO, P2O5, TiO2, and Sr concentrations. This covariation of Sri, Ndi and chemistry can be modeled by a process of simple mixing of basaltic and granitic magmas having weight percent SiO2 of 48.0 and 73.3 respectively. Isotopic characteristic of the mafic magma are Sri=0.7047, Ndi=0.51269 andδ18O=6.0, and of the felsic magma are Sri=0.7068, Ndi=0.51212 andδ18O=8.9. The rocks sampled contain from 50 to 80% of the felsic component. An aplite in the outer equigranular unit of the Tuolumne Intrusive Suite apparently was derived by fractional crystallization of plagioclase and hornblende from magma with granudiorite composition that was a product of mixing of the magmas described above. Siliceous magmas derived from the lower crust, having a maximum of 15 percent mantle-derived mafic component, are represented by the inner prophyritic units of the Tuolumne Intrusive Suite.

Experimental constraints on depths of fractionation of mildly alkalic basalts and associated felsic rocks: Pantelleria, Strait of Sicily

Abstract: Pantelleria, Italy, is a continental rift volcano consisting of alkalic basalt, trachyte, and pantellerite. At 1 atm along the FMQ buffer, the least-evolved basalt (Mg #= 58.5% norm ne) yields olivine on the liquidus at ∼1,180° C, followed by plagioclase, then by clinopyroxene, and by titanomagnetite and ilmenite at ∼ 1,075°. After ∼70% crystallization, the residual liquid at ∼1,025° is still basaltic and also contains apatite and possibly kaersutite. A less alkalic basalt shows the same order of phase appearance. Glass compositions define an Fe-enrichment trend and a density maximum for anhydrous liquids that coincides with a minimum in Mg#.

Theoretical phase relations involving cordierite and garnet revisited: the influence of oxygen fugacity on the stability of sapphirine and spinel in the system Mg-Fe-Al-Si-O

Abstract: The theoreticalP-T grid for stability relations of the phases cordierite (Cd), sapphirine (Sa), hypersthene (Hy), garnet (Ga), spinel (Sp), sillimanite (Si), and quartz (Qz) of Hensen (1971), has proved useful in the interpretation of metamorphic mineral assemblages formed at low oxygen fugacity. Both experimental data and evidence from natural rocks indicate that at high oxygen fugacity compatability relations change as a result of the enlargement of the stability field of spinel, which causes a topological inversion and the stabilisation of the invariant points [Sa], [Ga], and [Cd]. This implies the stable existence of the univariant equilibria (for\(f_{{\text{O}}_{\text{2}} } \) buffered conditions): Sp+Qz=Ga+Hy+Si+O2 (Sa, Cd), Cd+Sp+Qz=Hy+Si+O2 (Sa, Ga) and Sa+Sp+Qz=Hy+Si+O2 (Ga, Cd) and the divariant reaction: Sp+Qz=Hy+Si+O2 (Sa, Ga, Cd). These redox equilibria are restricted to conditions of high oxygen fugacity. The proposed theoreticalP-T grids, for both low and high oxygen fugacity, satisfactorily explain all experimental data and metamorphic mineral assemblages so far found in granulites.

Subduction-related shoshonitic and ultrapotassic magmatism; a study of Siluro-Ordovician syenites from the Scottish Caledonides

Abstract: Syenites are important or predominant components of several plutonic complexes, emplaced between 456 and 415 Ma along the NW margin of the Caledonian orogenic belt, adjacent to the Lewisian foreland, in W and NW Scotland. Although there are, in detail, chemical differences between the syenites from each centre, they form a well-defined compositional group overall. Ratios amongst their trace elements (especially very high values of La/Nb) are quite different from those trachytes and syenites formed by fractional crystallisation of ocean-island basalts and their continental equivalents, emplaced in regions of anorogenic crustal tension. Instead, the Scottish Caledonian syenites closely resemble chemically the fractional-crystallisation residua of potassic subduction-related magmas, such as the shoshonitic series. A comendite minor intrusion from a swarm associated with the Loch Borralan and Loch Ailsh syenitic complexes is remarkably similar in composition to Recent obsidian from the shoshonitic volcano of Lipari, in the Aeolian Arc. Published Sr- and Pb-isotopic ratios preclude a significant component of either upper (Proterozoic Moine schists) or lower crust (granulite-facies Archaean Lewisian or Proterozoic Grenvillian gneisses) in all these syenites, except in local syenitic facies of the Glenelg-Ratagain complex. Fractional crystallisation appears to be the mechanism by which the liquids which formed these syenites evolved from basic parental magmas. The phases involved in this process may have included plagioclase, alkali feldspar, pyroxene, amphibole, biotite, garnet, Fe-Ti oxide, sphene, allanite, apatite, zircon and zirconolite, and therefore all the ratios amongst even the so-called incompatible elements may have changed during the evolution of the leucocratic magmas. Nevertheless, a detailed study of the Glen Dessarry complex shows that the changes are insufficient to disguise the geochemical nature of the parental magmas. These appear to be picritic shoshonite (MgO> 15%, Ni>400ppm, La/Yb∼20, La/Nb>5) for the Glen Dessarry, Loch Borralan and Loch Ailsh syenites, and picritic ultrapotassic magmas (MgO>15%, Ni>400 ppm, La/ Yb∼60, La/Nb>7) — such as would crystallise to minettes — for the Loch Loyal and Glenelg-Ratagain syenites. Mafic shoshonites were erupted amongst the 410 Ma Lome lavas of this region and also occur as widespread approximately-contemporaneous volcanic feeder plugs. Minettes of similar age are also common as dykes in NW Scotland. Numerous large tonalite-granite complexes, with minor diorites and gabbros, were emplaced in W and NW Scotland between 435 and 400 Ma. These are generally acknowledged to be mixtures of magmas from crustal and mantle sources. Their more mafic members show compositional features, such as very high Ba and Sr, which group them with the rare syenites and the Lorne lavas of the same region into a distinctive geochemical province, within which shoshonitic and allied magmas were the mantle-derived component. Two models are presented to account for the generation of strongly-potassic, subduction-related magmas several hundred km behind a NW-directed subduction zone, or during the period immediately following continental collision.

Age and evolution of the Grenville Province in eastern Labrador from U-Pb systematics in accessory minerals

Abstract: U-Pb isotope analysis of zircon, titanite, monazite and rutile extracted from 15 different Grenville Province rocks in eastern Labrador reveals: 1) major crust formation through magmatism between 1,710 and 1,630 Ma ago; no evidence of older crustal material was found. 2) Pegmatite and gabbro intrusions between 1,500 and 1,400 Ma ago, probably related to incomplete rifting of the earlier formed crust. 3) Granite and syenite plutonism, presumably anorogenic, circa 1,300 Ma ago. 4) High grade metamorphism and anatexis during the Grenvillian Orogeny, causing Pb-loss in primary zircon and new growth of zircon, titanite and monazite at circa 1,030 Ma ago in the south (Lake Melville and Mealy Mountains terranes) and circa 970 Ma ago in the north (Groswater Bay Terrane and Trans-Labrador Batholith); geochronological distinction of these large-scale crustal segments substantiates their juxtaposition along deeply rooted, intracontinental ductile thrust zones during Grenvillian Orogeny. 5) Late Grenvillian growth of rutile in gabbros circa 925 Ma ago.

The dynamics of magma-mixing during flow in volcanic conduits

Abstract: The production of mixed magmas (streaky pumice) during flow in a volcanic conduit has been modelled in the laboratory by studying the flow of two miscible fluids of differing viscosity passing concentrically through a vertical pipe. In the experiments reported in this paper, the outermost fluid is the more viscous, as would be the case when two magmas are simultaneously tapped from a zoned chamber in which silicic magma overlies mafic magma. At a Reynolds number (Re) which is much less than that required for turbulence in isoviscous pipe flow, the interface between two liquids of different viscosity can become unstable. Growth of the instability and mixing proceed when Re, based on the properties of the inner, less viscous fluid (Re i), is greater than approximately 3 if between 10% and 90% of the flowing fluid is composed of the more viscous fluid. Outside this range of flow rate ratios, higher Re i and viscosity ratios are required to ensure mixing. When the viscosity ratio U≤10 the unstable flow takes the form of an asymmetric, sinusoidal wave and at higher viscosity ratios axisymmetric, bead-like waves are the dominant instability. Entrainment across the boundaries of these wavy interfaces results in the production of streaky mixtures of the two liquids. The degree of mixing increases with Re 1, U and distance downstream. Application of experimental results to magmatic situations shows that mixing will be possible in eruptions which tap layers of different viscosity from a stratified chamber. If a volcanic feeder is allowed to become lined by silicic magma before a mafic magma layer is drawn up from the chamber then a mixed pumice (or lava) sequence will ensue. Alternatively, if draw-up occurs when the feeder is still propagating away from the chamber, the slower flowing silicic magma may be overtaken by the faster flowing mafic magma. The advancing conduit will then have mafic or hybrid chilled margins enclosing a silicic interior, i.e. the usual arrangement in composite dykes and sills. Simultaneous tapping of silicic and underlying mafic magmas from a chamber can thus lead to magma mixing and to the emplacement of either mixed pumice sequences or composite intrusions, depending on the history of magma withdrawal and the dynamics of flow in the conduit.

Anhydrous P-T phase relations of near-primary high-alumina basalt from the South Sandwich Islands

Abstract: Anhydrous P-T phase relations, including phase compositions and modes, are reported from 10–31 kbar for a near-primary high-alumina basalt from the South Sandwich Islands in the Scotia Arc The water content of natural subduction-related basalt is probably 27 kbar) garnet is the liquidus phase followed by clinopyroxene, then quartz/coesite at lower temperatures At intermediate pressures (17–27 kbar), clinopyroxene is the liquidus phase followed by either garnet, quartz, plagioclase, then orthopyroxene or plagioclase, quartz, garnet, then orthopyroxene depending on the pressure within this interval At all lower pressures, plagioclase is the liquidus phase followed at much lower temperatures (∼100° C at 5 kbar) by clinopyroxene The absence of olivine from the liquidus suggests that the composition studied here could not have been derived from a more mafic parent by olivine fractionation at any pressure investigated, and supports the interpretation that it is primary If so, these results also preclude an origin for this melt by partial melting of olivine-rich mantle periddotite and suggest instead that it was generated by partial melting of the descending slab (quartz eclogite) leaving clinopyroxene, garnet, or both in the residue The generally flat REE patterns for low-K series subduction related basalts argue against any significant role for garnet, however, and it is thus concluded that the composition studied here was extracted at 20–27 kbar after sufficiently high degrees of partial melting (∼50%) to totally consume garnet in the eclogite source Melting experiments on three MORB composition, although not conclusive, are in agreement with this mechanism Results at 30 kbar support an origin for tonalite/trondhjemite series rocks by lower degrees of melting (15–30%), leaving both garnet and clinopyroxene in the residue

Western Fiordland orthogneiss: Early Cretaceous arc magmatism and granulite facies metamorphism, New Zealand

Abstract: U-Pb isotopic analyses of zircons from a distinctive suite of previously undated granulite facies metaplutonic rocks, here termed the Western Fiordland Orthogneiss (WFO), in Fiordland, southwest New Zealand, indicate synkinematic magmatic emplacement between ∼120 and 130 Ma ago. These rocks were previously interpreted as possibly being of Precambrian age. Initial Pb and Sr ratios are consistent with arc/subduction related magmagenesis with little or no involvement of ancient continental crust. Subsequent high pressure (>12 kb) metamorphism of the WFO may reflect a major collision event involving crustal thickening by overthrusting of a >15 km thick sequence. Metamorphism ceased ≤116 Ma ago based on206Pb/238U ages of zircon from a retrogressed granulite. U-Pb isotopic analysis of apatite, along with previously published Rb/Sr mineral ages, indicate that final uplift and cooling to <300–400° C was largely completed by ∼90 Ma. The average uplift rate during this period is inferred to have been in excess of 1 mm/yr. Unmetamorphosed gabbronorites of the Darran Complex in eastern Fiordland, inferred by some investigators to be the granulite protolith, yield concordant U/Pb zircon ages of 137±1 Ma. U-Pb ages of apatite, and previously published K/Ar mineral ages indicate that these rocks experienced a rapid and simple cooling history lasting only a few million years. The high-grade WFO and unmetamorphosed Darran Complex are now separated by a profound structural break. However, the ages and similarities in initial Pb and Sr isotopic ratios suggest that both suites are products of the same Early Cretaceous cycle of subduction-related magmatism. The timing of Early Cretaceous magmatism and metamorphism, collision and resultant crustal thickening, and subsequent great uplift and erosion in Fiordland has important implications for terrane accretion and the evolution of relative plate motions along the New Zealand segment of the Gondwana margin.

Effect of stirring on crystallization kinetics of basalt: texture and element partitioning

Abstract: Isothermal crystallization experiments on basalt have been carried out using an infrared heating furnace to investigate the effect of stirring. When stirring was not applied (static experiment), the results agreed well with previous experiments. But when stirring was applied and a flow of Reynolds number=10−3∼−4 was present (dynamic experiment), considerably different results were obtained, especially in respect to the nucleation rate and the morphology of crystals. At ΔT=25° C essentially similar results were obtained on the nucleation rates and morphologies of crystals in both static and dynamic experiments. However, at supercoolings larger than 45° C, nucleation density increased drastically in dynamic experiments reaching up to ten times as large as that in static experiments. Crystals of plagioclase and clinopyroxene were small and adapted acicular morphology regardless of ΔT in dynamic experiments, and hyalopilitic textures were formed. A TTT-diagram shows that the nucleation incubation time is shorter in dynamic experiments than in static experiments. No compositional difference in major elements was found in plagioclase and clinopyroxene produced in both static and dynamic experiments. However, minor element concentrations, e.g., Mg in plagioclase and Ti, Al in clinopyroxene, were found to increase with both ΔT and flow velocity. All these results imply that although chemical diffusion in the melts did not play an important role in the dynamic experiments, interface kinetics were important. It is suggested that hyalopilitic texture commonly seen in natural basalt is mainly due to flow in magma.

Zirconolite, allanite and hoegbomite in a marble skarn from the Bergell contact aureole: implications for mobility of Ti, Zr and REE

Abstract: Zirconolite, allanite and hoegbomite are present as accessory phases in a metasomatically altered spinel-calcite-marble from the contact with the Bergell intrusives (Switzerland/Italy). Textural relationships indicate a step-wise alteration of spinel to 1) hoegbomite or corundum + magnetite, 2) margarite and 3) chlorite. Replacement of spinel by hoegbomite can be described by the substitution 1.94(Mg2+, Fe2+, Zn2+, Mn2+, Ca2+)⇋Ti4+ +0.12(OH−) where Al3+ and Fe3+ are held constant. The average composition of the Bergell hoegbomites is given by the formula Fe 0.97 2+ Mg0.69Zn0.04Ti0.17Al3.94Fe 0.06 3+ O7.98(OH)0.02 and seems to be imposed by the composition of pre-existing spinel. During the first two steps of spinel alteration, calcite was replaced by anorthite+phlogopite, and the rare earth element(REE)-bearing minerals zirconolite, allanite and sphene were formed. Allanites have characteristic chondrite-normalized REE patterns with enrichment in the light REE. The zirconolite patterns show a marked increase in concentration from La to Ce, followed by an almost constant section. Sphene lacks detectable La, and its REE patterns vary from grain to grain. Contemporaneous formation of phlogopite, REE-bearing minerals and hoegbomite during replacement of the spinel-calcite-marble indicates that the metamorphic fluid introduced potassium along with REE and other high valence cations (Ti4+, Zr4+, U4+, Th4A3804265, Nb5A3804265, Y3A3804265) possibly as polynuclear complexes. The abundance of fluorine-bearing phlogopite and fluor-apatite as well as their close association with REE-bearing minerals and hoegbomite suggests F− and PO 4 3− as likely ligands for complexing of the above mentioned elements.

The Pb-Sr-Nd isotope geochemistry of some recent circum-Mediterranean granites

Abstract: Pb, Sr and Nd isotopic compositions have been analyzed in recent granites from Northern Africa, Northern Italy and Greece. Lead isotope compositions of K-feldspars are rather homogeneous, and cluster close to the modern lead of Stacey and Kramers (1975) but with slightly higher207Pb/204Pb and208Pb/204Pb ratios. The Cyclades samples, however, have higher206Pb/204Pb ratios. Addition of mantle-derived lead was probably very limited, which supports a quasi-closed system evolution of this element in the continental crust. The Sr, Nd data fall in the enriched part of the143Nd/144Nd vs.87Sr/86Sr diagram and define a smooth hyperbolic mixing curve. Over a wide area, straddling different orogens, most granites may be accounted for by a binary mixture between a recycled crustal component and a depleted mantle-like component. No correlation is observed between either Pb and Sr or Nd isotopic ratios, or any isotopic ratio and major element contents. Quantitative modelling suggests that two cases fit the Sr and Nd characteristics of these granites: they both require anatexis of the crust on a scale large enough to average the isotopic properties of heterogeneous terranes. In the first case, the mantle-derived component may be represented by differentiated Island Arc-type magmas, and the granites result from mixing these magmas with anatectic melts. In the second case, mantle-derived igneous rocks, such as obducted ophiolites, are part of the crustal source and their variable involvement in the anatectic process causes isotopic variations.

Precise U-Pb zircon ages for the Molson dyke swarm and the Fox River sill: Constraints for Early Proterozoic crustal evolution in northeastern Manitoba, Canada

Abstract: Precise U-Pb zircon ages have been obtained for samples from the Molson dyke swarm and the Fox River sill in NE Manitoba, Canada. The ages determined for the Cross Lake and Cuthbert Lake dykes are 1,883.7−1.5+1.7and 1,883±2 Ma, respectively, and are in excellent agreement with the 1,882.9−1.4+1.5Ma age obtained for the Fox River sill. These results support the contention that the emplacement of the Fox River sill and the Molson Dyke swarm was contemporaneous and also demonstrate the potential for correlating mafic igneous activity in widely spaced localities. The timing of Early Proterozoic mafic magmatism in the western Superior Province appears to be synchronous with igneous activity in other parts of the Circum-Superior Belt and in the Trans Hudson orogen to the west. The emplacement of the Molson dyke swarm at 1,883 Ma indicates a 700 Ma interval of quiescence between the final igneous activity that is recorded in the Archean basement and dyke intrusion. The presence of deformed equivalents of Molson dykes in the Thompson Nickel Belt indicates that the intense deformation in this belt occurred sometime after 1,883 Ma.

Nd and Sr isotopes in the Aleutians: multicomponent parenthood of island-arc magmas

Abstract: Young volcanic rocks from different sections of the Aleutian Islands-Alaska Peninsula Arc have been measured for 87Sr/86Sr, 143Nd/144Nd and some trace elements. We found the 143Nd/144Nd to be highly restricted in range (ɛ Nd=6 to 7) and low as compared to midocean ridge ba-salts (MORB). This indicates that the source of the Aleutian Arc magmas is different from MORB and remarkably isotopically homogeneous with respect to Nd. The range reported here for arc rocks is substantially smaller than found by other workers. However, the Sr isotope ratios vary considerably (ɛ Sr=−24 to −14). Those samples from small volcanic centers north of the main arc (second arc) are characterized by low ɛ Sr. Our data in combination with previous studies suggest that there are slight geochemical differences between discrete sections of the arc. The general uniformity of Nd isotope ratios are thought to be the surface expression of an efficient mixing or homogenization process beneath the arc plate, but which still causes a wide dispersion in Sr isotopic composition. To relate the arc rocks to the broader tectonic setting and to identify possible sources of arc magmas, measurements were done on volcanic and sedimentary rocks from the North Pacific/Bering Sea area. Alkali basalts from the back-arc islands St. George, Nunivak and St. Lawrence and alkali-rich tholeiites from the fore-arc have ɛ Nd=+4 to +9 and are correlated on the ɛ Sr-ɛ Nddiagram parallel to the mantle array but shifted to lower ɛ Sr. These samples are thought to be isotopically representative of the mantle transported to that region. A tholeiitic basalt from the Kamchatka Basin ocean floor (back-arc), however, yielded typical MORB values (ɛ Nd=10, ɛ Sr=−24). Composite sediment samples were made from DSDP cores in the Aleutian Abyssal Plain, Gulf of Alaska and the Alka Basin which represent mixtures of continentally and arc-derived materials. These composites have intermediate Nd isotopic (ɛ Nd= −2 and +2) and high Sr isotopic values (ɛ Sr=+9 and +37). These data show that possible source materials of the Aleutian Arc volcanics are isotopically different from and much more heterogeneous than the arc rocks themselves. On the basis of this study and of literature data, we developed a set of alternative models for volcanic arc magma generation, based on the restricted range in ɛ Nd and the wider range in ɛ Sr for arc rocks. Different isotopic and trace element characteristics found in different arcs or arc sections are explained by varying mixing proportions or concentrations in source materials. The basic observations require rather strict mixing ratios to obtain constant ɛ Nd. The preferred model is one where the melting of subducted oceanic crust is controlled by the amount of trapped sediment with the melting restricted to the upper part of the altered basaltic layer. Homogenization within the upper part of the oceanic crust is brought about by hydrothermal circulation attending dewatering of the slab during subduction and possibly some oxygen exchange of the magmas on ascent.

Petrogenesis of Monte Vulture volcano (Italy): inferences from mineral chemistry, major and trace element data

Abstract: The paper presents major and trace element data and mineral compositions for a series of foiditic-tephritic to phonolitic rocks coming from Monte Vulture, Southern Italy, and investigates their origin, evolution and relationship with the other centres of the Roman province. Major and trace element variation in the foiditic to tephritic suite agrees with a hypothesis of evolution by simple crystal/liquid fractionation, whereas the early erupted phonolitic trachytes and phonolites have geochemical characteristics which do not support their derivation from tephritic magma by crystal fractionation. Foiditic and phonolitic rocks have mineral compositions which are interpreted as indicating magma mixing. However geochemical evidence shows that this process did not play an important role during the magma evolution. The Vulture rocks have compositional peculiarities such as high abundance of Na2O, CaO, Cl and S, when compared with other Roman volcanics. Instead, the distribution of incompatible elements is similar to those of Roman rocks, except for a lower content of Rb and K, higher P and lower Th/Ta and Th/Nb ratios which are still close to the values of arc volcanics. The high contents of Na, Ca and of volatile components are tentatively attributed to the interaction of magma with aqueous solutions, rich in calcium sulphate and sodium chloride, related to the Miocene or Triassic evaporites occurring within the sedimentary sequence underlying the volcano. The distribution pattern of the incompatible elements is interpreted as indicative of magma-forming in a subduction modified upper mantle and of the peculiar location of M. Vulture.

Early Archaean Amîtsoq tonalites and granites of the Isukasia area, southern West Greenland: development of the oldest-known sial

Abstract: Amphibolite facies early Archaean Amitsoq gneisses envelop and intrude the c. 3,800 Ma Isua supracrustal belt, Isukasia area, southern West Greenland. Most of these gneisses are strongly deformed, but in a c. 75 km2 augen of lower deformation, the Amitsoq gneisses are seen to comprise predominantly 3,750–3,700 Ma tonalitic grey gneisses that were intruded first by thin bodies of mafic to dioritic composition, known collectively as the Inaluk dykes, and then by c. 3,600 Ma white gneisses and finally by sporadic c. 3,400 Ma pegmatitic gneiss sheets. The grey gneisses could have formed by partial melting of crust consisting predominantly of basic rocks. The Inaluk dykes are interpreted as strongly fractionated basic melts of mantle origin, contaminated by crustal material. The white gneisses consist mostly of medium grained granite and occur as lenses and anastomosing sheets throughout their host of grey gneisses with subordinate inclusions of supracrustal rocks. The white gneisses have chemistry compatible with formation by partial melting at depth of a source dominated by grey gneisses. The igneous chemistry, including REE abundances, of the grey gneisses and white gneisses has been modified to varying degrees by metasomatism and assimilation reactions during the crystallisation of the white gneisses and also during subsequent tectonometamorphic events. The white gneisses are evidence for considerable reworking by anatexis of sialic crust in the early Archaean, 150 to 100 Ma after its formation. The white gneisses and the pegmatitic gneisses show that granitic rocks s.s. were important in the earliest Archaean, and are further evidence of the diversity of the oldest-known sial.