Geochemistry and petrogenesis of the Gallego Volcanic Field,Solomon Islands,SW Pacific and geotectonic implications

The Upper Miocene to present day Gallego Volcanic Field (GVF) is located in northwest Guadalcanal, Solomon Islands, SW Pacific, and potentially includes the offshore Savo volcano. The GVF is a multi-centred complex covering an area of ~ 800 km² on Guadalcanal and a further ~ 30 km² on the island of Savo, north of west Guadalcanal. GVF volcanism is characterised by effusive eruptions of lava, intrusion of sub-volcanic plutons, as well as pyroclastic flow and fall deposits dominated by block and ash flow deposits. Geochemical analysis of a representative suite of samples from the GVF demonstrates that the GVF comprise largely a ‘main suite’ of basalts to andesites and minor trachyandesites. The predominant mineralogy of the GVF comprises plagioclase, amphibole, clinopyroxene and magnetite-ilmenite. Associated with the ‘main suite’ are cognate nodules composed of hornblendite, gabbros, and clinopyroxenite. Interpretation of major and trace element geochemistry and petrographic studies suggests that fractionation was dominated by early clinopyroxene, and later amphibole + clinopyroxene + minor plagioclase. Geochemical features such as the incompatibility of Sr suggest that plagioclase largely crystallised en-masse late in the fractionation sequence. The presence of amphibole and late fractionation of plagioclase is suggestive of derivation from initially water-rich magmas. The region is characterised by strong geographically-related geochemical variations as evidenced by the Woodlark (and Manus) basins: basalts become more arc-like within the ocean basins with decreasing distance to the subducting trench. The GVF-Savo volcanoes are spatially and geochemically affected by deep N-S fractures that show some evidence of sympathetic geochemical variations with distance from the trench (e.g. Sr/Y ratios). Comparison with a range of international data for Th/Nb vs Pb/Nb and Dy/Yb vs SiO₂ indicate that: amphibole was indeed a strong controlling phase on magmatic evolution; garnet had no obvious role; there was little sediment input into the source region; that relative Pb/Nb enrichments may be linked to similar enrichments within the subducting Woodlark basin (and by analogy with the Manus basin and its abundant hydrothermal Pb-rich sulphide deposits); and the predominant influence on the source region for GVF-Savo was from metasomatic fluids and/or melts from the slab subducting at the southern trench.     

From basalt to dacite: origin and evolution of the calc-alkaline series of Salina, Aeolian Arc, Italy

The island of Salina comprises one of the most distinct calc-alkaline series of the Aeolian arc (Italy), in which calc-alkaline, high-K calc-alkaline, shoshonitic and leucite-shoshonitic magma series are developed. Detailed petrological, geochemical and isotopic (Sr, Nd, Pb, O) data are reported for a stratigraphically well-established sequence of lavas and pyroclastic rocks from the Middle Pleistocene volcanic cycle (430–127 ka) of Salina, which is characterized by an early period of basaltic volcanism (Corvo; Capo; Rivi; Fossa delle Felci, group 1) and a sequence of basaltic andesites, and andesites and dacites in the final stages of activity (Fossa delle Felci, groups 2–8). Major and trace element compositional trends, rare earth element (REE) abundances and mineralogy reveal the importance of crystal fractionation of plagioclase + clinopyroxene + olivine/ orthopyroxene ± titanomagnetite ± amphibole ± apatite in generating the more evolved magma types from parental basaltic magmas, and plagioclase accumulation in producing the high Al₂O₃ contents of some of the more evolved basalts. Sr isotope ratios range from 0.70410 to 0.70463 throughout the suite and show a well-defined negative correlation with ¹⁴³Nd/¹⁴⁴Nd (0.51275–0.51279). Pb isotope compositions are distinctly radiogenic with relatively large variations in ²⁰⁶Pb/²⁰⁴Pb (19.30–19.66), fairly constant ²⁰⁷Pb/²⁰⁴Pb (15.68–15.76) and minor variations in ²⁰⁸Pb/²⁰⁴Pb ratios (39.15–39.51). Whole-rock δ¹⁸O values range from +6.4 to +8.5‰ and correlate positively with Sr isotope ratios. Overall, the isotopic variations are correlated with the degree of differentiation of the rocks, indicating that only small degrees of crustal assimilation are overprinting the dominant evolution by crystal–liquid fractionation (AFC-type processes). The radiogenic and oxygen isotope composition of the Salina basalts suggests derivation from primary magmas from a depleted mantle source contaminated by slab-derived fluids and subducted sediments with an isotopic signature of typical upper continental crust. These magmas then evolved further to andesitic and dacitic compositions through the prevailing process of low-pressure fractional crystallization in a shallow magma reservoir, accompanied by minor assimilation of crustal lithologies similar to those of the Calabrian lower crust. Received: 29 November 1999 / Accepted: 16 April 2000     

Quaternary minettes and associated volcanic rocks of Mascota,western Mexico: a consequence of plate extension above a subduction modified mantle wedge

 Pleistocene-Holocene volcanism in the Jalisco block of western Mexico is confined to two conspicuous grabens, where potassic eruptives range from absarokites (48–52% SiO₂) and minettes (49–54% SiO₂) through basaltic andesites (53–57% SiO₂), the most voluminous type, to andesites and their lamprophyric equivalent spessartite (58–62% SiO₂); there are no contemporary rhyolitic rocks. This suite has high concentrations of Mg, Cr (<550 ppm) and Ni (<450 ppm) accompanied by large concentrations of K, P, Ba (<4000 ppm) and Sr (<5000 ppm) and elements such as LREE and Zr (<600 ppm). No combination of crystal fractionation and/or crustal contamination can reproduce the compositional range of these magmas, which nevertheless are believed to be genetically related because of their proximity in time and space. Hydrous minerals in the lamprophyres and the typical absence of plagioclase phenocrysts in both basaltic andesites and andesites reflect the relatively high concentrations of water in the magmas, which suppressed the crystallisation of feldspar. Experimental verification of the minimal amounts of water required to reproduce the phenocryst assemblages in selected rocks range from 3.5 to 6%. During ascent in a volcanic conduit, andesitic magma may lose water and consequently precipitate plagioclase, or it may ascend more rapidly, retaining more of its initial water, which stabilises phenocrysts of hornblende at the expense of plagioclase. Our estimates of water concentrations, which are consistent with the various low pressure phenocryst assemblages, will be minimal for the magmas in their source regions, and the process of magmatic dewatering on ascent may be typical in well established volcanic conduits. In accord with the compositions of phenocrystic olivine in the basaltic andesites and the minettes, the values of FeO and Fe₂O₃ of the bulk lavas and scoriae are demonstrably pristine. As a consequence, there are two characteristic features of the Mascota suite: the high range of relative oxygen fugacities (ΔNNO=1–5) and the high Mg# (MgO/MgO+FeO) that ranges from 0.70 to 0.91 (with only one andesite as low as 0.66). From the evidence of phlogopite phenocrysts, a partial melt involving phlogopite would have a higher Mg# than one from olivine (Fo₉₀) and pyroxene alone. As the Mascota series shows a correlation between K₂O and Mg#, we conclude that it was generated by partial fusion of the mantle wedge, with a variable contribution of phlogopite and apatite from veins throughout the lherzolitic assemblage. In conformity with an origin by varying increments of partial fusion of a phlogopite-bearing mantle, all incompatible elements vary linearly with Ti (or K) as if phlogopite (+apatite) in the source dominated their contribution to the partial melts. Fluids from dehydration of the subducting slab presumably deposit hydrous and other minerals in veins in the mantle wedge and also increase its redox state. As the Mascota volcanism occurs in grabens closer to the trench than the main andesite arc, it is concluded that the eruption of these small volumes of hydrous magmas require the tectonically favored ascent paths offered by the extensional grabens to reach the surface from their mantle sources. Received: 24 January 1995 / Accepted: 21 February 1996     

Garnet-bearing tonalitic porphyry from East Kunlun,Northeast Tibetan Plateau: implications for adakite and magmas from the MASH Zone

A garnet-bearing tonalitic porphyry from the Achiq Kol area, northeast Tibetan Plateau has been dated by SHRIMP U-Pb zircon techniques and gives a Late Triassic age of 213 ± 3 Ma. The porphyry contains phenocrysts of Ca-rich, Mn-poor garnet (CaO > 5 wt%; MnO < 3 wt%), Al-rich hornblende (Al₂O₃ ~ 15.9 wt%), plagioclase and quartz, and pressure estimates for hornblende enclosing the garnet phenocrysts yield values of 8–10 kbar, indicating a minimum pressure for the garnet. The rock has SiO₂ of 60–63 wt%, low MgO (<2.0 wt%), K₂O (<1.3 wt%), but high Al₂O₃ (>17 wt%) contents, and is metaluminous to slightly peraluminous (ACNK = 0.89–1.05). The rock samples are enriched in LILE and LREE but depleted in Nb and Ti, showing typical features of subduction-related magmas. The relatively high Sr/Y (~38) ratios and low HREE (Yb < 0.8 ppm) contents suggest that garnet is a residual phase, while suppressed crystallization of plagioclase and lack of negative Eu anomalies indicate a high water fugacity in the magma. Nd–Sr isotope compositions of the rock (εNd_T = −1.38 to −2.33; ⁸⁷Sr/⁸⁶Sr_i = 0.7065–0.7067) suggest that both mantle- and crust-derived materials were involved in the petrogenesis, which is consistent with the reverse compositional zoning of plagioclase, interpreted to indicate magma mixing. Both garnet phenocrysts and their ilmenite inclusions contain low MgO contents which, in combination with the oxygen isotope composition of garnet separates (+6.23‰), suggests that these minerals formed in a lower crust-derived felsic melt probably in the MASH zone. Although the rock samples are similar to adakitic rocks in many aspects, their moderate Sr contents (<260 ppm) and La/Yb ratios (mostly 16–21) are significantly lower than those of adakitic rocks. Because of high partition coefficients for Sr and LREE, fractionation of apatite at an early stage in the evolution of the magma may have effectively decreased both Sr and LREE in the residual melt. It is suggested that extensive crystallization of apatite as an early phase may prevent some arc magmas from evolving into adakitic rocks even under high water fugacity.     

Early Cretaceous highly positive <Emphasis Type="Italic">ε</Emphasis><Subscript>Nd</Subscript> felsic volcanic rocks from the Hinggan Mountains,NE China: origin and implications for Phanerozoic crustal growth

An early Cretaceous (135 ± 2 Ma) felsic volcanic suite of dacite and rhyolite from Huolinhe, NE China is characterized by large ion lithophile element and light REE enrichment and high field strength element (HFSE, e.g., Nb and Ta) and Ti–P depletion, and bulk silicate earth-like Sr [⁸⁷Sr/⁸⁶Sr(i) = 0.70409–0.70481], quite radiogenic Nd [ε _Nd(t) = +3.98 to +5.88], Pb [e.g., ²⁰⁶Pb/²⁰⁴Pb(i) = 18.46–18.55] and Hf [ε _Hf(t) ~+9.2] isotope compositions. Compared with contemporaneous mafic rocks in the region, these felsic rocks have even higher Nd and Hf isotopic ratios, precluding an origin through differentiation of coeval mantle-derived magmas. Isotope calculation results suggest that these magmas were derived from a preexistent mixture composed of mainly juvenile crust (70–80%), and a subordinate recycled crustal component (20–30%) having highly radiogenic Sr and Pb and unradiogenic Nd and Hf. About 25–30% melting of such a mixed source produced the primary dacitic magma. The rhyolites, which have relatively low MgO, FeO*, Al₂O₃, CaO, TiO₂, P₂O₅, Na₂O, Ba, Sr, REE, HFSE and Y, were differentiates of the dacites after removal of a fractional assemblage of hornblende + plagioclase + K-feldspar + apatite + zircon. Considering the prolonged events (from 262 to 130 Ma) that produced such highly positive ε _Nd felsic igneous rocks in the region, we prefer a pre-Mesozoic crustal growth model related to arc accretion associated with the Paleo-Asian Ocean subduction.     

The processes that control leucosome compositions in metasedimentary granulites: perspectives from the Southern Marginal Zone migmatites,Limpopo Belt,South Africa

Anatexis of metapelitic rocks at the Bandelierkop Quarry (BQ) locality in the Southern Marginal Zone of the Limpopo Belt occurred via muscovite and biotite breakdown reactions which, in order of increasing temperature, can be modelled as: (1) Muscovite + quartz + plagioclase = sillimanite + melt; (2) Biotite + sillimanite + quartz + plagioclase = garnet + melt; (3) Biotite + quartz + plagioclase = orthopyroxene ± cordierite ± garnet + melt. Reactions 1 and 2 produced stromatic leucosomes, which underwent solid‐state deformation before the formation of undeformed nebulitic leucosomes by reaction 3. The zircon U–Pb ages for both leucosomes are within error identical. Thus, the melt or magma formed by the first two reactions segregated and formed mechanically solid stromatic veins whilst temperature was increasing. As might be predicted from the deformational history and sequence of melting reactions, the compositions of the stromatic leucosomes depart markedly from those of melts from metapelitic sources. Despite having similar Si contents to melts, the leucosomes are strongly K‐depleted, have Ca:Na ratios similar to the residua from which their magmas segregated and are characterized by a strong positive Eu anomaly, whilst the associated residua has no pronounced Eu anomaly. In addition, within the leucosomes and their wall rocks, peritectic garnet and orthopyroxene are very well preserved. This collective evidence suggests that melt loss from the stromatic leucosome structures whilst the rocks were still undergoing heating is the dominant process that shaped the chemistry of these leucosomes and produced solid leucosomes. Two alternative scenarios are evaluated as generalized petrogenetic models for producing Si‐rich, yet markedly K‐depleted and Ca‐enriched leucosomes from metapelitic sources. The first process involves the mechanical concentration of entrained peritectic plagioclase and garnet in the leucosomes. In this scenario, the volume of quartz in the leucosome must reflect the remaining melt fraction with resultant positive correlation between Si and K in the leucosomes. No such correlation exists in the BQ leucosomes and in similar leucosomes from elsewhere. Consequently, we suggest disequilibrium congruent melting of plagioclase in the source and consequential crystallization of peritectic plagioclase in the melt transfer and accumulation structures rather than at the sites of biotite melting. This induces co‐precipitation of quartz in the structures by increasing SiO₂ content of the melt. This process is characterized by an absence of plagioclase‐induced fractionation of Eu on melting, and the formation of Eu‐enriched, quartz + plagioclase + garnet leucosomes. From these findings, we argue that melt leaves the source rapidly and that the leucosomes form incrementally as melt or magma leaving the source dumps its disequilibrium Ca load, as well as quartz and entrained ferromagnesian peritectic minerals, in sites of magma accumulation and escape. This is consistent with evidence from S‐type granites suggesting rapid magma transfer from source to high level plutons. These findings also suggest that leucosomes of this type should be regarded as constituting part of the residuum from partial melting.     

High-Ti amphibole as a petrogenetic indicator of magma chemistry: evidence for mildly alkalic-hybrid melts during evolution of Variscan basic–ultrabasic magmatism of Central Iberia

Central Iberian Variscan granite batholiths and anatectic complexes are punctuated by coeval stocks of hydrous, high-K calc-alkaline, ultrabasic to intermediate rock series. Despite their overall calc-alkaline affinity, the mafic–ultramafic members contain high-Ti amphibole oikocrysts rimmed by lower-Ti amphibole ± cummingtonite and high-Ti amphibole replacing early phlogopite. To understand the factors controlling the saturation of high-Ti amphibole in the parental magmas, clinopyroxene-melt, phlogopite-melt and amphibole-melt relationships are reviewed. This analysis reveals that for melts with intermediate compositions, the affinity of TiO₂ for amphibole rises in alkalic magmas. Accordingly, mildly alkalic trachytoid to subalkaline medium- to high-K andesite and dacite compositions are estimated for interstitial high-Ti amphibole-saturated melts. Amphibole Ce/Pb ratios reveal a mantle–crust hybrid nature for interstitial melts with subalkaline trachytoid compositions. The hydrous character of the Variscan basic magmas favoured an overall magmatic evolutionary trend with a low rate of variation of Na₂O with respect to silica during amphibole crystallization. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Cumulate xenoliths from St. Vincent, Lesser Antilles Island Arc: a window into upper crustal differentiation of mantle-derived basalts

In order to shed light on upper crustal differentiation of mantle-derived basaltic magmas in a subduction zone setting, we have determined the mineral chemistry and oxygen and hydrogen isotope composition of individual cumulus minerals in plutonic blocks from St. Vincent, Lesser Antilles. Plutonic rock types display great variation in mineralogy, from olivine–gabbros to troctolites and hornblendites, with a corresponding variety of cumulate textures. Mineral compositions differ from those in erupted basaltic lavas from St. Vincent and in published high-pressure (4–10 kb) experimental run products of a St. Vincent high-Mg basalt in having higher An plagioclase coexisting with lower Fo olivine. The oxygen isotope compositions (δ¹⁸O) of cumulus olivine (4.89–5.18‰), plagioclase (5.84–6.28‰), clinopyroxene (5.17–5.47‰) and hornblende (5.48–5.61‰) and hydrogen isotope composition of hornblende (δD = −35.5 to −49.9‰) are all consistent with closed system magmatic differentiation of a mantle-derived basaltic melt. We employed a number of modelling exercises to constrain the origin of the chemical and isotopic compositions reported. δ¹⁸O_Olivine is up to 0.2‰ higher than modelled values for closed system fractional crystallisation of a primary melt. We attribute this to isotopic disequilibria between cumulus minerals crystallising at different temperatures, with equilibration retarded by slow oxygen diffusion in olivine during prolonged crustal storage. We used melt inclusion and plagioclase compositions to determine parental magmatic water contents (water saturated, 4.6 ± 0.5 wt% H₂O) and crystallisation pressures (173 ± 50 MPa). Applying these values to previously reported basaltic and basaltic andesite lava compositions, we can reproduce the cumulus plagioclase and olivine compositions and their associated trend. We conclude that differentiation of primitive hydrous basalts on St. Vincent involves crystallisation of olivine and Cr-rich spinel at depth within the crust, lowering MgO and Cr₂O₃ and raising Al₂O₃ and CaO of residual melt due to suppression of plagioclase. Low density, hydrous basaltic and basaltic andesite melts then ascend rapidly through the crust, stalling at shallow depth upon water saturation where crystallisation of the chemically distinct cumulus phases observed in this study can occur. Deposited crystals armour the shallow magma chamber where oxygen isotope equilibration between minerals is slowly approached, before remobilisation and entrainment by later injections of magma.     

Phenocryst complexity in andesites and dacites from the Tequila volcanic field,Mexico: resolving the effects of degassing vs. magma mixing

The petrology of five phenocryst-poor (2–5%) andesites and dacites, all of which were erupted from different short-lived, monogenetic vents, is compared to that of phenocryst-rich (10–25%) andesites erupted from the adjacent stratovolcano, Volcán Tequila, in the Mexican arc. Despite differences in phenocryst abundances, these magmas have comparable phase assemblages (plagioclase + orthopyroxene + titanomagnetite + ilmenite + apatite ± augite ± hornblende), and similarly wide variations in phenocryst compositions, coupled to complex zoning patterns. For the phenocryst-poor lavas, equilibrium pairs of two Fe–Ti oxides lead to a narrow range of calculated temperatures for each sample that range from 934 (±24) to 1,073 (±6)°C and oxygen fugacities that range from +0.1 to +0.7 log units relative to the Ni–NiO buffer. Application of the plagioclase-liquid hygrometer to each sample at these calculated temperatures leads to maximum melt water concentrations of 4.6–3.1 wt% during plagioclase crystallization, indicating that the magmas were fluid saturated at depths ≥6.4–4.5 km. There is a wide, continuous range in the composition of plagioclase (≤44 mol% An) and orthopyroxene (≤16% Mg#) phenocrysts in each sample, which is consistent with a loss of dissolved water (≤2.8 wt%) from the melt phase during degassing as the magmas ascended rapidly to the surface. Evidence is presented that shows the effect of dissolved water is to reduce the activity of MgO relative to FeO in the melt phase, which indicates that degassing will also affect the Mg# of pyroxene phenocrysts, with higher melt water concentrations favoring Fe-rich pyroxene. Both plagioclase and orthopyroxene commonly display diffusion-limited growth textures (e.g., skeletal and hopper crystals, large interior melt hollows, and swallow tails), which are consistent with large undercoolings produced by degassing-induced crystallization. Therefore, degassing is proposed as a possible cause for the phenocryst compositional diversity documented in the phenocryst-poor andesite and dacite lavas erupted from peripheral vents, including the coexistence of normally zoned plagioclase and reversely zoned orthopyroxene. Degassing-induced crystallization may also explain some of the phenocryst complexity in crystal-rich andesites erupted from large stratovolcanoes, including Volcán Tequila.     

Coeval potassic and sodic calc-alkaline series in the post-collisional Hercynian Tanncherfi intrusive complex, northeastern Morocco: geochemical, isotopic and geochronological evidence

The post-collisional late Hercynian Tanncherfi intrusive complex (TIC) is part of a widespread intrusive episode in the Moroccan Meseta. The complex contains a wide range of rock types, from monzogabbros to monzogranites. Two distinct magmatic series are recognized: (1) a potassic (shoshonitic) series consisting of monzogabbros, quartz monzonites and monzogranites; and (2) a sodic (granodioritic) series represented by quartz monzodiorites and granodiorites. All the Tanncherfi plutonic rocks display similar spider-diagram profiles, with LILE and LREE enrichment and Nb, Ta, Ti depletion, which are typical of subduction-related magmas. Combined major, trace element compositions and Sr, Nd isotopic results indicate that the two series have been derived from a LILE- and LREE-enriched continental lithospheric mantle source, under different partial melting and/or depth conditions. Intrusion of the Tanncherfi rocks was not temporally related to subduction and the enrichment of their source is likely to be linked to preceding subduction events. The two series evolved by fractional crystallization, of clinopyroxene, plagioclase, hornblende, biotite, K-feldspar and accessories (Fe–Ti oxide minerals, titanite, apatite and zircon) for the potassic series while the sodic series combined fractional crystallization with assimilation of felsic magmas with lower Sr isotopic ratio than the more mafic term of the series, the quartz monzodiorite. The intrusion of the potassic magmas (344±6 Ma) marks a major change in the tectonic regime of eastern Meseta. These magmas intruded during post-thickening uplift and extension, both probably favored by convective thinning of the lithosphere. This model provides a reasonable mechanism for the genesis of other Hercynian intrusive complexes in Morocco.     

K-feldspar–quartz and K-feldspar–plagioclase phase boundary interactions in garnet–orthopyroxene gneiss's from the Val Strona di Omegna, Ivrea–Verbano Zone, northern Italy

A detailed study based on textural observations combined with microanalysis [back scattered electron imaging (BSE) and electron microprobe analysis (EMPA)] and microstructural data transmission electron microscopy (TEM) has been made of K-feldspar micro-veins along quartz–plagioclase phase and plagioclase–plagioclase grain boundaries in granulite facies, orthopyroxene–garnet-bearing gneiss's (700–825 °C, 6–8 kbar) from the Val Strona di Omegna, Ivrea–Verbano Zone, northern Italy. The K-feldspar micro-veins are commonly associated with quartz and plagioclase and are not found in quartz absent regions of the thin section. This association appears to represent a localised reaction texture resulting from a common high grade dehydration reaction, namely: amphibole + quartz = orthopyroxene + clinopyroxene + plagioclase + K-feldspar + H₂O, which occurred during the granulite facies metamorphism of these rocks. There are a number of lines of evidence for this. These include abundant Ti-rich biotite, which was apparently stable during granulite facies metamorphism, and total lack of amphibole, which apparently was not. Disorder between Al and Si in the K-feldspar indicates crystallisation at temperatures >500 °C. Myrmekite and albitic rim intergrowths in the K-feldspar along the K-feldspar–plagioclase interface could only have formed at temperatures >500–600 °C. Symplectic intergrowths of albite and Ca-rich plagioclase between these albitic rim intergrowths and plagioclase suggest a high temperature grain boundary reaction, which most likely occurred at the start of decompression in conjunction with a fluid phase. Relatively high dislocation densities (>2 × 10⁹ to 3 × 10⁹/cm²) in the K-feldspar suggest plastic deformation at temperatures >500 °C. We propose that this plastic deformation is linked with the extensional tectonic environment present during the mafic underplating event responsible for the granulite facies metamorphism in these rocks. Lastly, apparently active garnet grain rims associated with side inclusions of K-feldspar and quartz and an exterior K-feldspar micro-vein indicate equilibrium temperatures within 20–30 °C of the peak metamorphic temperatures estimated for the sample (770 °C). Contact between these K-feldspar micro-veins and Fe-Mg silicate minerals, such as garnet, orthopyroxene, clinopyroxene or biotite along the interface, is observed to be very clean with no signs of melt textures or alteration to sheet silicates. This lends support to the idea that these micro-veins did not originate from a melt and, if fluid induced, that the water activity of these fluids must have been relatively low. All of these lines of evidence point to a high grade origin for the K-feldspar micro-veins and support the hypothesis that they formed during the granulite facies metamorphism of the metabasite layers in an extensional tectonic environment as the consequence of localised dehydration reactions involving the breakdown of amphibole in the presence of quartz to orthopyroxene, clinopyroxene, plagioclase, K-feldspar and H₂O. It is proposed that the dehydration of the metabasite layers to an orthopyroxene–garnet-bearing gneiss over a 4-km traverse in the upper Val Strona during granulite facies metamorphism was a metasomatic event initiated by the presence of a high-grade, low H₂O activity fluid (most likely a NaCl–KCl supercritical brine), related to the magmatic underplating event responsible for the Mafic Formation; and that this dehydration event did not involve partial melting. Received: 15 February 2000 / Accepted: 26 June 2000     

Petrology, isotope geochemistry and chemical budgets of oceanic gabbros-seawater interactions in the Equatorial Atlantic

 Petrological and chemical variations, as well as oxygen and strontium isotopic data are presented for metagabbros from the Romanche and Vema fracture zones. These rocks were affected by several types and degrees of alterations ranging from slight hydrothermal alteration to complete amphibolitization. Five major kinds of alteration processes ranging from late-magmatic deuteric alteration (stage I) to low temperature (<150 °C) alteration (stage V) were identified. Water-rock interactions between 300 and 650 °C are the most dominant interactions resulting in the most prevailing secondary mineralogical assemblages which characterize the amphibolite and/or greenschist facies (amphibole ± plagioclase ± epidote ± titanite ± chlorite ± prehnite). Hydrothermal alteration of these gabbroic rocks results in isotopic exchanges between rocks and seawater-derived fluids. These exchanges lead to decrease of gabbroic δ¹⁸O toward values as low as +3.9‰, and larger Sr isotopic variations than other oceanic gabbroic rocks (⁸⁷Sr/⁸⁶Sr ratios shift to 0.7029–0.7051). Calculation of a chemical budget indicates that metagabbros are hydrated and enriched in Fe and probably in Mg and Cl, while Si, Ca and Ti are released to the hydrothermal fluids. In addition to metamorphic recrystallization and geochemical transformation, hydrothermal alteration of oceanic gabbros contributes to the control of the global ocean geochemistry. Received: 8 March 1999 / Accepted: 12 July 1999     

Petrogenesis of the Puerto Edén Igneous and Metamorphic Complex,Magallanes, Chile: Late Jurassic syn-deformational anatexis of metapelites and granitoid magma genesis

A suite of schists, gneisses, migmatites, and biotite granitoids from the Puerto Edén Igneous and Metamorphic Complex (PEIMC) and biotite–hornblende granitoids of the South Patagonian batholith (southern Chile) has been studied. For that purpose, the chemistry of minerals and the bulk rock composition of major and trace elements including Rb–Sr and Sm–Nd isotopes were determined. Mineralogical observations and geothermobarometric calculations indicate high-temperature and low-pressure conditions (ca. 600–700 °C and 3 to 4.5 kbar) for an event of metamorphism and partial melting of metapelites in Late Jurassic times (previously determined by SHRIMP U–Pb zircon ages). Structures in schists, gneisses, migmatites and mylonites indicate non-coaxial deformation flow during and after peak metamorphic and anatectic conditions. Andalusite schists and sillimanite gneisses yield initial ⁸⁷Sr/⁸⁶Sr ratios of up to 0.7134 and εNd₁₅₀ values as low as − 7.6. Contemporaneous biotite granitoids and a coarse-grained orthogneiss have initial ⁸⁷Sr/⁸⁶Sr ratios between 0.7073 and 0.7089, and εNd₁₅₀ values in the range − 7.6 to − 4.4. This indicates that metamorphic rocks do not represent the natural isotopic variation in the migmatite source. Thus, a heterogeneous source with a least radiogenic component was involved in the production of the biotite granitoids. The PEIMC is considered as a segment of an evolving kilometre-sized and deep crustal shear zone in which partial melts were generated and segregated into a large reservoir of magmas forming composite plutons in Late Jurassic times. A biotite–hornblende granodiorite and a muscovite–garnet leucogranite show initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7048 and 0.7061, and εNd₁₀₀ values of − 2.6 and − 1.8, respectively, and are thus probably related to Early Cretaceous magmas not involved in the anatexis of the metasedimentary rocks.     

Origin of silicic volcanism in the Panamanian arc: evidence for a two-stage fractionation process at El Valle volcano

In the Central American Volcanic Arc, adakite-like volcanism has often been described as volumetrically insignificant. However, extensive silicic adakitic volcanism does occur in the Panamanian arc and provides an opportunity to evaluate the origin of this magma-type as well as to contrast its origin with other Central American silicic magmas. The Quaternary volcanic deposits of El Valle volcano are characterized by pronounced depletions in the heavy rare earth elements, low Y, high Sr, high Sr/Y, relatively high MgO, and low K₂O/Na₂O, when compared with other Quaternary Central American volcanics at similar SiO₂. These chemical features are also diagnostic of adakitic signatures. Our new ⁴⁰Ar/³⁹Ar ages of lava flows and ash flows that compose the volcanic edifice of El Valle volcano illustrate that the eruptive volume of adakitic-like volcanism is substantial during the Quaternary (~120 km³). Adakitic-like magmas dominate the stratigraphic record. Common to all models for the origin of an adakite geochemical signature is the involvement of garnet, as a residual or fractionating phase. The stability of garnet in hydrous magmas has been recently reevaluated with important consequences; garnet is a stable primary igneous phase at pressure and temperature conditions expected for magma differentiation at the roots of a mature island arc. Moreover, adakite-like volcanism erupted at El Valle volcano displays the middle rare earth element depletion observed in other Panamanian volcanic centers that has been attributed to significant amphibole fractionation. Extensive amphibole fractionation may have occurred in two stages. The first stage of fractionation, garnet + amphibole fractionation, occurs from hydrous basaltic–andesitic parental magmas that have ponded at the base of an overthickened crust. The second stage occurs at mid-lower crustal levels where abundant amphibole + plagioclase and minor sphene crystallized from water-rich magmas. These two stages combined may have resulted in an amphibole-rich cumulate layer. This amphibole layer is likely the source of the abundant amphibole-rich cumulate enclaves and blobs found in volcanic products across the Panamanian arc. Stalling of water-rich magmas during this two-stage fractionation process could drive the interstitial liquids to the evolved compositions typical of continental crust, while leaving behind amphibole-rich cumulate rocks that may eventually be returned to the asthenosphere. Differentiation of H₂O-rich magmas under the conditions appropriate for the roots of island arcs may therefore be a key process in developing a better understanding of the generation of continental crust in island arc environments.     

Petrogenesis of mafic microgranular enclaves (MMEs) in the oligocene-miocene granitoid plutons from northwest Anatolia,Turkey

Mafic microgranular enclaves (MMEs) in host granitoids can provide important constraints on the deep magmatic processes. The Oligocene-Miocene granitoid plutons of the NW Anatolia contain abundant MMEs. This paper presents new hornblende Ar-Ar ages and whole-rock chemical and Sr-Nd isotope data of the MMEs from these granitic rocks. Petrographically, the MMEs are finer-grained than their host granites and contain the same minerals as their host rocks (amphibole + plagioclase + biotite + quartz + K-feldspar), but in different proportions. The Ar-Ar ages of the MMEs range from 27.9 ± 0.09 Ma to 19.3 ± 0.01 Ma and are within error of their respective host granitoids. The MMEs are metaluminous and calc-alkaline, similar to I-type granites. The Sr-Nd isotopes of MMEs are 0.7057 to 0.7101 for ⁸⁷Sr/⁸⁶Sr and 0.5123 to 0.5125 for ¹⁴³Nd/¹⁴⁴Nd, and are similar to their respective host granitoids. These lithological, petrochemical and isotopic characteristics suggest that the MMEs in this present study represent chilled early formed cogenetic hydrous magmas produced during a period of post-collisional lithospheric extension in NW Anatolia. The parental magma for MMEs and host granitoids might be derived from partial melting of underplated mafic materials in a normally thickened lower crust in a post-collisional extensional environment beneath the NW Anatolia. Delamination or convective removal of lithospheric mantle generated asthenospheric upwelling, providing heat and magma to induce hydrous re-melting of underplated mafic materials in the lower crust.     

Transition from fracturing to viscous flow in granulite facies perthitic feldspar (Lofoten,Norway)

Recrystallization of perthites in granulite facies (T = 700–730 °C, P = 0.65–0.8 GPa) shear zones in mangerite-charnockite rocks from Lofoten (Norway) is localized along intracrystalline bands parallel to fractures. Fracturing preferentially occurred along the cleavage planes (010) and (001). EBSD analysis of perthite porphyroclasts indicates a very low degree of internal misorientation (within 5°) and the lack of recovery features. Recrystallized grains show coarsening with increasing width of the bands, and chemical changes with respect to the host grains. Crystallographic orientation of the new grains does not show a host-control relation to the parent perthite grains. In summary, the microstructure and CPO data consistently indicate intragranular recrystallization by nucleation and growth from fractured grains. Perthite porphyroclasts are surrounded by a matrix of recrystallized plagioclase + K-feldspar ± amphibole ± biotite. There is extensive evidence of syndeformational nucleation of new phases and of phase boundary migration in the matrix, with plagioclase grains forming bulges and protrusions towards K-feldspar. The spatial distribution of K-feldspar and plagioclase in the recrystallized matrix is characterized by the predominance of phase boundaries over grain boundaries. All these observations are consistent with diffusion creep as the dominant deformation mechanism in the matrix, associated with grain boundary sliding. Accordingly, recrystallized plagioclase and K-feldspar show a very weak crystallographic preferred orientation, which is interpreted in terms of oriented growth during diffusion creep. Fracturing of perthites promoted extensive grain size reduction, recrystallization, fluid infiltration, and operation of grain-size sensitive creep, resulting in strain localization.     

An overview on geochemistry of Proterozoic massif-type anorthosites and associated rocks

A critical study of 311 published WR chemical analyses, isotopic and mineral chemistry of anorthosites and associated rocks from eight Proterozoic massif anorthosite complexes of India, North America and Norway indicates marked similarities in mineralogy and chemistry among similar rock types. The anorthosite and mafic-leucomafic rocks (e.g., leuconorite, leucogabbro, leucotroctolite, anorthositic gabbro, gabbroic anorthosite, etc.) constituting the major part of the massifs are characterized by higher Na₂O + K₂O, Al₂O₃, SiO₂, Mg# and Sr contents, low in plagioclase incompatible elements and REE with positive Eu anomalies. Their δ ¹⁸O‰ (5.7–7.5), initial ⁸⁷Sr/⁸⁶Sr (0.7034–0.7066) and ɛ _Nd values (+1.14 to +5.5) suggest a depleted mantle origin. The Fe-rich dioritic rocks occurring at the margin of massifs have isotopic, chemical and mineral composition more close to anorthosite-mafic-leucomafic rocks. However, there is a gradual decrease in plagioclase content, An content of plagioclase and X_Mg of orthopyroxene, and an increase in mafic silicates, oxide minerals content, plagioclase incompatible elements and REE from anorthosite-mafic-leucomafic rocks to Fe-rich dioritic rocks. The Fe-rich dioritic rocks are interpreted as residual melt from mantle derived high-Al gabbro melt, which produced the anorthosite and mafic-leucomafic rocks. Mineralogically and chemically, the K-rich felsic rocks are distinct from anorthosite-mafic-leucomafic-Fe-rich dioritic suite. They have higher δ ¹⁸O values (6.8–10.8‰) and initial ⁸⁷Sr/⁸⁶Sr (0.7067–0.7104). By contrast, the K-rich felsic suites are products of melting of crustal precursors.     

High-Grade Fluid Metasomatism on both a Local and a Regional Scale: the Seward Peninsula, Alaska, and the Val Strona di Omegna, Ivrea-Verbano Zone, Northern Italy. Part I: Petrography and Silicate Mineral Chemistry

K-feldspar–plagioclase–quartz mineral textures aswell as biotite and hornblende compositions are compared forsuites of metamorphosed mafic rocks from two widely separatedtraverses. A portion of either traverse has experienced a high-gradedehydration event transforming it from an H₂O-rich, hornblende-bearingzone to an H₂O-poor, hornblende-free, orthopyroxene-bearing,‘granulite facies’ zone at 700–800°C and7–8 kbar. In the Kigluaik Mountains, Seward Peninsula,Alaska, dehydration took place over an 85 cm thick layer ofmetatonalite in contact with a marble during regional metamorphismand involved a CO₂-rich fluid, whereas for the Val Strona diOmegna traverse, Ivrea–Verbano Zone, northern Italy, dehydrationtook place over a 3–4 km thick sequence of metabasitesinterlayered with metapelites in a contact metamorphic eventinvolving basaltic magmas intruded at the base of the sequence.Orthopyroxene-bearing samples from both dehydration zones showmicro-veins of K-feldspar along quartz and plagioclase grainboundaries as well as replacement antiperthite in plagioclase.K came primarily from the breakdown of hornblende + quartz toorthopyroxene ± clinopyroxene, feldspar and fluid. Biotiteeither was stabilized or formed in the dehydration zones andis enriched in Ti, Mg, F and Cl relative to biotite in the amphibolitefacies zone. KEY WORDS: KCl–NaCl brines; metasomatism; granulite facies metamorphism; charnockite–enderbite; orthopyroxene; K-feldspar; biotite; hornblende     

Polygenetic titanite records the composition of metamorphic fluids during the exhumation of ultrahigh‐pressure metagranite in the Sulu orogen

An integrated study of U–Pb ages and trace elements was carried out for titanite and zircon from ultrahigh‐pressure (UHP) metagranites in the Sulu orogen, east‐central China. The results provide constraints on the composition of metamorphic fluids during the exhumation of deeply subducted continental crust. Titanite has two domain types based on REE patterns and trace element variations, Ttn‐I and Ttn‐II respectively. These two domains show indistinguishable U–Pb ages of 232 ± 14 to 220 ± 8 Ma, in general agreement with anatectic zircon U–Pb ages of 223 ± 4 to 219 ± 2 Ma for the partial melting event during early exhumation. The Ttn‐I domains have significantly higher REE, Th, Ta and Sr, and higher Th/U ratios than the Ttn‐II domains, indicating that the two domains have grown from metamorphic fluids with different compositions. For the Ttn‐I domains, Zr‐in‐titanite thermometry yields high temperatures of 773–851 °C at 2.5 GPa, and petrographic observations reveal the presence of melt pseudomorphs. Thus, they are interpreted to have grown from hydrous melts in the early exhumation stage. In contrast, the Ttn‐II domains were texturally equilibrated with amphibolite facies minerals such as biotite and plagioclase and contain inclusions of plagioclase and quartz. The Zr‐in‐titanite thermometry yields lower temperatures of 627–685 °C at 1.0 GPa. In combination with their REE patterns, they are interpreted to have grown from aqueous solutions at amphibolite facies metamorphic conditions during further exhumation. The differences in Th and Sr contents are prominent between the Ttn‐I and Ttn‐II domains, signifying the compositional difference between the hydrous melts and aqueous solutions. Therefore, the polygenetic titanite in the UHP metamorphic rocks provides insights into the geochemical property of metamorphic fluids during the continental subduction‐zone processes.     

Petrogenesis of Sierra Nevada plutons inferred from the Sr, Nd, and O isotopic signatures of mafic igneous complexes in Yosemite Valley, California

Mafic complexes in the central Sierra Nevada batholith record valuable geochemical information regarding the role mafic magmas play in arc magmatism and the generation of continental crust. In the intrusive suite of Yosemite Valley, major and trace element compositions of the hornblende-bearing gabbroic rocks from the Rockslides mafic complex and of the mafic dikes in the North America Wall are compositionally similar to high-alumina basalt. Of these rocks, two samples have higher Ni and Cr abundances as well as higher ε_Nd values than previously recognized for the intrusive suite. Plagioclase crystals in rocks from the North America Wall and the Rockslides have prominent calcic cores and sharply defined sodic rims, a texture commonly associated with mixing of mafic and felsic magmas. In situ analyses of ⁸⁷Sr/⁸⁶Sr in plagioclase show no significant isotopic difference from the cores to the rims of these grains. We propose that the high ⁸⁷Sr/⁸⁶Sr (~0.7067) and low ε_Nd (~?3.4) of bulk rocks, the homogeneity of ⁸⁷Sr/⁸⁶Sr in plagioclase, and the high δ¹⁸O values of bulk rocks (6.6–7.3 ‰) and zircon (Lackey et al. in J Petrol 49:1397–1426, 2008) demonstrate that continental crust was assimilated into the sublithospheric mantle-derived basaltic precursors of the mafic rocks in Yosemite Valley. Contamination (20–40 %) likely occurred in the lower crust as the magma differentiated to high-alumina basalt prior to plagioclase (and zircon) crystallization. As a consequence, the isotopic signatures recorded by whole rocks, plagioclase, and zircon do not represent the composition of the underlying lithospheric mantle. We conclude that the mafic and associated felsic members of the intrusive suite of Yosemite Valley represent 60–80 % new additions to the crust and include significant quantities of recycled ancient crust.