Petrogenesis of Adakitic Porphyries in an Extensional Tectonic Setting, Dexing, South China: Implications for the Genesis of Porphyry Copper Mineralization

The Dexing adakitic porphyries (quartz diorite–granodioriteporphyries), associated with giant porphyry Cu deposits, arelocated in the interior of a continent (South China). They exhibitrelatively high MgO, Cr, Ni and Sr contents, high La/Yb andSr/Y ratios, but low Yb and Y contents, similar to adakitesproduced by slab melting associated with subduction. However,they are characterized by bulk Earth-like Nd–Sr isotopecompositions (_Nd(t) = –1·14 to +1·80 and(⁸⁷Sr/⁸⁶Sr)_i = 0·7044 – 0·7047), and highTh (12·6–27·2 ppm) contents and Th/Ce (0·19–0·94)ratios, which are different from those of Cenozoic slab-derivedadakites. Sensitive High-Resolution Ion Microprobe (SHRIMP)geochronology studies of zircons reveal that the Dexing adakiticporphyries have a crystallization age of 171 ± 3 Ma.This age is contemporaneous with Middle Jurassic extension withinthe Shi-Han rift zone, and within-plate magmatism elsewherein South China, indicating that the Dexing adakitic porphyrieswere probably formed in an extensional tectonic regime in theinterior of the continent rather than in an arc setting. Theirhigh Th contents and Th/Ce ratios, and Middle Jurassic age,argue against an origin from a Neoproterozoic (1000 Ma) stalledslab in the mantle. Taking into account available data for theregional metamorphic–magmatic rocks, and the present-daycrustal thickness (31 km) in the area, we suggest that the Dexingadakitic porphyries were most probably generated by partialmelting of delaminated lower crust, which was possibly triggeredby upwelling of the asthenospheric mantle due to the activityof the Shi-Hang rift zone. Moreover, the Dexing adakitic magmasmust have interacted with the surrounding mantle peridotiteduring their ascent, which elevated not only their MgO, Cr andNi contents, but also the oxygen fugacity (fO₂) of the mantle.The high fO₂ could have induced oxidation of metallic sulfidesin the mantle and mobilization of chalcophile elements, whichare required to produce associated Cu mineralization. Therefore,the Cu metallogenesis associated with the Dexing adakitic porphyriesis probably related to partial melting of delaminated lowercrust, similar to the metallogenesis accompanying slab melting. KEY WORDS: adakite; lower crust; delamination; porphyry copper deposit, South China     

Magmatic Evolution of the La Pacana Caldera System, Central Andes, Chile: Compositional Variation of Two Cogenetic, Large-Volume Felsic Ignimbrites

La Pacana is one of the largest known calderas on Earth, andis the source of at least two major ignimbrite eruptions witha combined volume of some 2700 km³. These ignimbrites have stronglycontrasting compositions, raising the question of whether theyare genetically related. The Toconao ignimbrite is crystal poor,and contains rhyolitic (76–77 wt % SiO₂) tube pumices.The overlying Atana ignimbrite is a homogeneous tuff whose pumiceis dacitic (66–70 wt % SiO₂), dense (40–60% vesicularity)and crystal rich (30–40 % crystals). Phase equilibriaindicate that the Atana magma equilibrated at temperatures of770–790°C with melt water contents of 3·1–4·4wt %. The pre-eruptive Toconao magma was cooler (730–750°C)and its melt more water rich (6·3–6·8 wt% H₂O). A pressure of 200 MPa is inferred from mineral barometryfor the Atana magma chamber. Isotope compositions are variablebut overlapping for both units (⁸⁷Sr/⁸⁶Sr_i 0·7094–0·7131;¹⁴³Nd/¹⁴⁴Nd 0·51222–0·51230) and are consistentwith a dominantly crustal origin. Glass analyses from Atanapumices are similar in composition to those in Toconao tubepumices, demonstrating that the Toconao magma could representa differentiated melt of the Atana magma. Fractional crystallizationmodelling suggests that the Toconao magma can be produced by30% crystallization of the observed Atana mineral phases. Toconaomelt characteristics and intensive parameters are consistentwith a volatile oversaturation-driven eruption. However, thelow H₂O content, high viscosity and high crystal content ofthe Atana magma imply an external eruption trigger. KEY WORDS: Central Andes; crystal-rich dacite; eruption trigger; high-silica rhyolite; zoned magma chamber     

Petrology of the Younger Andesites and Dacites of Iztacc?huatl Volcano, Mexico: II. Chemical Stratigraphy, Magma Mixing, and the Composition of Basaltic Magma Influx

The Younger Andesites and Dacites of Iztacc?huatl volcano, Mexico,constitute a medium-K calcalkaline rock suite (58–66 wt.per cent SiO₂) characterized by high Mg-numbers (100Mg/(Mg+0?85Fe²⁺=55–66) and relatively high abundances of MgO (2?5–6?6wt. per cent), Ni(17–158 p.p.m.), and Cr (42–224p.p.m.). Chemical stratigraphy plots of eruptive sequences indicatethe existence of a plexus of long-lived dacite magma chambersperiodically replenished by influxes of basaltic magma ascendingfrom depth. Short-term geochemical evolution after batch influxwas dictated by magma mixing and eventual dilution of the basalticcomponent by ‘quasi-steady state’ hornblende dacitemagma. The chemical data support textural and mineralogicalevidence for rapid homogenization of originally diverse magmasby convective blending of residual liquids accompanied by dynamicfractional crystallization (Nixon, 1988). Internally-consistent mixing calculations used to derive thecomposition of basaltic magma influx incorporate analyticaluncertainties and the observed range of salic end-member compositions.Mafic end-members are basalts to basaltic andesites (52–54wt. per cent SiO₂) with Mg-numbers (73–76), MgO (9–11wt. per cent), Ni (250 p.p.m.), and Cr (340–510 p.p.m.)concentrations, and liquidus olivine compositions (Fo_90–88),appropriate for unfractionated partial melts of mantle peridotite.The majority of model compositions are Ol-Hy-normative, similarto those of primitive basaltic lavas on the flanks of Iztacc?huatland in the Valley of Mexico. However, calculated magma batchesrange from weakly Qz-normative to strongly Ne-normative. Bothcalculated and analyzed basaltic compositions are distinguishedby highly variable abundances of alkalies and incompatible traceelements, notably Rb, Ba, Sr, P, Zr, and Y. Initial ⁸⁷Sr/⁸⁶Sr ratios for Iztacc?huatl lavas (0?7040–0?7046;n=24) are comparable to those for primitive basaltic rocks (0?7037–0?7045;?=4) and indicate that (1) mantle source regions are isotopicallyheterogeneous; and (2) contamination of iztacc?huatl magma chambersby radiogenic crustal rocks was not a significant factor inthe evolution of calc-alkaline andesites and dacites. The replenishment of Iztacc?huatl dacite reservoirs by Ne-normativemagmas late in the history of cone growth precludes exhaustionof mantle source regions by progressive partial melting. Thewaning stages of volcanic activity at Iztacc?huatl appear toreflect the inability of dense basaltic influxes to successfullypenetrate a large high-level chamber of low density hornblendedacite magma.     

A North-South Transect across the Central Mexican Volcanic Belt at ~100{degrees}W: Spatial Distribution, Petrological, Geochemical, and Isotopic Characteristics of Quaternary Volcanism

Within the Zitácuaro–Valle de Bravo (ZVB) regionof the central Mexican Volcanic Belt (MVB), three lava serieshave erupted during the Quaternary: (1) high-K₂O basaltic andesitesand andesites; (2) medium-K₂O basaltic andesites, andesitesand dacites; (3) high-TiO₂ basalts and basaltic andesites. Thedominant feature of the first two groups is the lack of plagioclaseaccompanying the various ferromagnesian phenocrysts (olivine,orthopyroxene, augite, and hornblende) in all but the dacites.This absence of plagioclase in the phenocryst assemblages ofthe high-K₂O and medium-K₂O intermediate lavas is significantbecause it indicates high water contents during the stage ofphenocryst equilibration. In contrast, the high-TiO₂ group ischaracterized by phenocrysts of plagioclase and olivine. Thespatial distribution of these three lava series is systematic.The southern section of the ZVB transect, 280–330 km fromthe Middle America Trench (MAT), is characterized by high-K₂Omelts that are relatively enriched in fluid-mobile elementsand have the highest ⁸⁷Sr/⁸⁶Sr ratios. Medium-K₂O basaltic andesiteand andesite lavas are present throughout the transect, butthose closest to the MAT are MgO-rich (3·5–9·4wt %) and have phenocryst assemblages indicative of high magmaticwater contents (3·5–6·5 wt % water) andrelatively low temperatures (950–1000°C). In markedcontrast, the northern section of the ZVB transect (380–480km from the MAT) has high-TiO₂, high field strength element(HFSE)-enriched magmas that have comparatively dry (< 1·5wt % magmatic water) and hot (1100–1200°C) phenocrystequilibration conditions. The central section of the ZVB transect(330–380 km from the MAT) is a transition zone and producesmoderately light rare earth element (LREE) and large ion lithophileelement (LILE)-enriched, medium-K₂O lavas with phenocryst assemblagesindicative of intermediate (1·5–3·5 wt %)water contents and temperatures. The high-K₂O series compositionsare the most enriched in LILE and LREE, with a narrow rangeof radiogenic ⁸⁷Sr/⁸⁶Sr from 0·704245 to 0·704507,¹⁴³Nd/¹⁴⁴Nd values ranging from 0·512857 to 0·512927(_Nd = 4·27–5·63), and ²⁰⁸Pb/²⁰⁴Pb valuesfrom 38·248 to 38·442, ²⁰⁷Pb/²⁰⁴Pb values from15·563 to 15·585, and ²⁰⁶Pb/²⁰⁴Pb values from18·598 to 18·688. The medium-K₂O series compositionsare only moderately enriched in the LILE and LREE, with a broaderrange of ⁸⁷Sr/⁸⁶Sr, but similar ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁸Pb/²⁰⁴Pbvalues to those of the high-K₂O series. In contrast, the high-TiO₂series compositions have little enrichment in LILE or LREE andinstead are enriched in the HFSE and heavy rare earth elements(HREE). The high-TiO₂ lavas are isotopically distinct in theirlower and narrower range of ¹⁴³Nd/¹⁴⁴Nd. The isotopic variationsare believed to reflect the upper mantle magma source regionsas the low content of phenocrysts in most lavas precludes significantupper crustal assimilation or magma mixing, other than thatrepresented by the presence of quartz xenocrysts (< 2 vol.%) with rhyolitic glass inclusions, which are found in manyof these lavas. The systematic spatial variation in compositionof the three lava series is a reflection of the underlying subduction-modifiedmantle and its evolution. KEY WORDS: central Mexico; geochemistry; isotopes; Quaternary volcanism; hydrous lavas     

Intra-Grain Sr Isotope Evidence for Crystal Recycling and Multiple Magma Reservoirs in the Recent Activity of Stromboli Volcano, Southern Italy

Over the last several hundred years, Stromboli has been characterizedby steady-state Strombolian activity. The volcanic productsare dominated by degassed and highly porphyritic (HP-magma)black scoria bombs, lapilli and lava flows of basaltic shoshoniticcomposition. Periodically (about one to three events per year),more energetic explosive eruptions also eject light colouredvolatile-rich pumices with low phenocryst content (LP-magma)that have more mafic compositions than the HP-magma. An in situmajor and trace element and Sr isotope microanalysis study ispresented on four samples chosen to characterize the differentmodes of activity at Stromboli: a lava flow (1985–1986effusive event), a scoria bomb from the ‘normal’present-day activity of Stromboli (April 1984), and a scoriaand coeval pumice sample from a recent more explosive eruption(September 1996). Plagioclase (An_62–90) and clinopyroxene(Mg-number between 0·69 and 0·91) phenocrystsin all samples record marked major element variations. Largeand comparable Sr isotope variations have been detected in plagioclaseand clinopyroxene. HP-magma crystals have resorbed cores, witheither high ⁸⁷Sr/⁸⁶Sr (0·70635–0·70630)or low ⁸⁷Sr/⁸⁶Sr (0·70614–0·70608); thelatter values are similar to the values of the outer cores.Mineral rims and glassy groundmasses generally have intermediate⁸⁷Sr/⁸⁶Sr (0·70628–0·70613). Similarly,mineral growth zones with three groups of ⁸⁷Sr/⁸⁶Sr values characterizeminerals from the LP-pumice, with the lowest values presentin mineral rims and groundmass glass. These results define amixing process between HP- and LP-magmas, plus crystallizationof clinopyroxene, plagioclase and olivine, occurring in a shallowmagma reservoir that feeds the present-day magmatic activityof Stromboli. An important observation is the presence of athird component (high ⁸⁷Sr/⁸⁶Sr in mineral cores) consideredto represent a pre-AD 1900 cumulus crystal mush reservoir situatedjust below the shallow magma chamber. These cumulus phases areincorporated by the LP-magma arriving from depth and transportedinto the shallow reservoir. A rapid decrease of ⁸⁷Sr/⁸⁶Sr inthe replenishing LP-magma immediately prior to eruption of theAD 1985 lava flow is associated with an increased volume ofLP-magma in the shallow magma chamber. The HP-magma in the shallowreservoir is not fully degassed when it interacts with the LP-magma,making efficient mixing possible that ultimately produces awell overturned homogeneous magma. Further degassing and crystallizationoccur at shallower levels as the HP-magma moves through a conduitto the surface. KEY WORDS: isotopic microsampling; mineral recycling; mixing; Sr isotope disequilibria; Stromboli     

Subduction Style Magmatism in a Non-subduction Setting: the Colville Igneous Complex, NE Washington State, USA

The Colville Igneous Complex is located within the Eocene MagmaticBelt of the North American Cordilleran interior. It straddlesthe US–Canadian border in northeast Washington and southernBritish Columbia. The complex consists of three intrusive andtwo extrusive phases, the first extrusive phase being contemporaneouswith the latter two intrusive phases. As a consequence of sub-solidusre-equilibration in the plutonic rocks, this study concentrateson the two extrusive phases, the Sanpoil Volcanic Formationand the Klondike Mountain Formation. The Sanpoil Volcanic Formationconsists of andesites, dacites and rare trachyandesites (SiO₂= 55–70 wt %) exhibiting a slight decrease in total alkalis(Na₂O + K₂O) with increasing silica. The Klondike Mountain Formationconsists of basalts, basaltic andesites, andesites, dacitesand rhyolites (SiO₂ = 51–75 wt %) with total alkalis increasingwith increasing silica. The calc-alkaline affinity of the rocksof the Colville Igneous Complex, coupled with the presence ofa ‘subduction signature’ of enriched large ion lithophileelements (LILE) and depleted high field strength elements (HFSE),has traditionally been attributed to petrogenesis in a subduction-relatedmagmatic arc, the ‘Challis Arc’. New trace and rareearth element and isotopic data (⁸⁷Sr/⁸⁶Sr_i,     

Kistufell: Primitive Melt from the Iceland Mantle Plume

This paper presents new geochemical data from Kistufell (64°48'N,17°13'W), a monogenetic table mountain situated directlyabove the inferred locus of the Iceland mantle plume. Kistufellis composed of the most primitive olivine tholeiitic glassesfound in central Iceland (MgO 10·56 wt %, olivine Fo_89·7).The glasses are interpreted as near-primary, high-degree plumemelts derived from a heterogeneous mantle source. Mineral, glassand bulk-rock (glass + minerals) chemistry indicates a low averagemelting pressure (15 kbar), high initial crystallization pressuresand temperatures (10–15 kbar and 1270°C), and eruptiontemperatures (1240°C) that are among the highest observedin Iceland. The glasses have trace element signatures (La_n/Yb_n<1, Ba_n/Zr_n 0·55–0·58) indicative ofa trace element depleted source, and the Sr–Nd–Pbisotopic ratios (⁸⁷Sr/⁸⁶Sr 0·70304–0·70308,¹⁴³Nd/¹⁴⁴Nd 0·513058–0·513099, ²⁰⁶Pb/²⁰⁴Pb18·343–18·361) further suggest a long-termtrace element depletion relative to primordial mantle. HighHe isotopic ratios (15·3–16·8 R/R_a) combinedwith low ²⁰⁷Pb/²⁰⁴Pb (15·42–15·43) suggestthat the mantle source of the magma is different from that ofNorth Atlantic mid-ocean ridge basalt. Negative Pb anomalies,and positive Nb and Ta anomalies indicate that the source includesa recycled, subducted oceanic crustal or mantle component. PositiveSr anomalies (Sr_n/Nd_n = 1·39–1·50) furthersuggest that this recycled source component involves lower oceaniccrustal gabbros. The     

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

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

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

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

Volcan Popocatepetl, Mexico. Petrology, Magma Mixing, and Immediate Sources of Volatiles for the 1994-Present Eruption

Volcán Popocatépetl has been the site of voluminousdegassing accompanied by minor eruptive activity from late 1994until the time of writing (August 2002). This contribution presentspetrological investigations of magma erupted in 1997 and 1998,including major-element and volatile (S, Cl, F, and H₂O) datafrom glass inclusions and matrix glasses. Magma erupted fromPopocatépetl is a mixture of dacite (65 wt % SiO₂, two-pyroxenes+ plagioclase + Fe–Ti oxides + apatite, 3 wt % H₂O, P= 1·5 kbar, f_O2 = NNO + 0·5 log units) and basalticandesite (53 wt % SiO₂, olivine + two-pyroxenes, 3 wt % H₂O,P = 1–4 kbar). Magma mixed at 4–6 km depth in proportionsbetween 45:55 and 85:15 wt % silicic:mafic magma. The pre-eruptivevolatile content of the basaltic andesite is 1980 ppm S, 1060ppm Cl, 950 ppm F, and 3·3 wt % H₂O. The pre-eruptivevolatile content of the dacite is 130 ± 50 ppm S, 880± 70 ppm Cl, 570 ± 100 ppm F, and 2·9 ±0·2 wt % H₂O. Degassing from 0·031 km³ of eruptedmagma accounts for only 0·7 wt % of the observed SO₂emission. Circulation of magma in the volcanic conduit in thepresence of a modest bubble phase is a possible mechanism toexplain the high rates of degassing and limited magma productionat Popocatépetl. KEY WORDS: glass inclusions; igneous petrology; Mexico; Popocatépetl; volatiles     

Magnesian andesites, Nb-enriched basalt-andesites, and adakites from late-Archean 2.7 Ga Wawa greenstone belts, Superior Province, Canada: implications for late Archean subduction zone petrogenetic processes

Magnesian andesites (MA) occur with 'normal' tholeiitic to calc-alkaline basalt-andesite suites in four greenstone belts of the 2.7 Ga Wawa subprovince, Canada. Collectively, the magnesian andesites span ranges of SiO₂=56-64 wt%, Mg-number=0.64-0.50, with Cr and Ni contents of 531-106 and 230-21 ppm, respectively. Relative to 'normal' andesites, the magnesian andesites form distinct trends on variation diagrams, with relatively high Th and LREE contents, uniform Yb over a range of MgO, more fractionated HREE, and lower Nb/Th_pm and Nb/La_pm ratios. Niobium-enriched basalts and andesites (NEBA; Nb=7-16 ppm), and an Al-enriched rhyolite (adakite) suite are associated in space and time with the magnesian andesites. Nb-enriched basalts and andesites are characterized by high TiO₂, P₂O₅, Th, and Zr contents, variably high Zr/Hf (36-44) ratios, and more fractionated HREE (Gd/Yb_cn=1.3-4.1) compared to the 'normal' tholeiitic to calc-alkaline basalt-andesite suites. The adakite suite has the high Al (Al₂O₃=16-18 wt%), high La/Yb_cn (21-43), and low Yb (0.4-1.2 ppm) of Archean tonalite-trondhjemite-granodiorite (TTG) suites and Cenozoic adakites, indicative of liquids derived mainly from slab melting. The basalt-andesite suites are not characterized by normal tholeiitic or calc-alkaline fractionation trends of major or trace elements. Rather, compositional trends can be accounted for by some combination of fractional crystallization and variable degrees of metasomatism of the source of basalt and/or andesites by adakitic liquids. The occurrence of magnesian andesites, Nb-enriched basalts/andesites, and adakites has been described from certain Phanerozoic arcs featuring shallow subduction of young and/or hot oceanic lithosphere. Adakites likely represent slab melts, magnesian andesites the product of hybridization of adakite liquids with mantle peridotite, and Nb-enriched basalts/andesites melts of the residue from hybridization. Geological similarities between the late-Archean Wawa greenstone belts and certain Cenozoic transpressional orogens with the MA-NEBA-adakite association suggest that subduction of young, hot oceanic lithosphere may have played an important role in the production of this arc-related association in the late Archean.     

The Cretaceous Igneous Province of Madagascar: Geochemistry and Petrogenesis of Lavas and Dykes from the Central-Western Sector

The Cretaceous lava sequence and associated mafic dyke swarmin central–western Madagascar (Mailaka and Bemaraha areas)range in composition from picrite basalts to cordierite–orthopyroxene-bearingrhyodacites (MgO from 14 to 0·6 wt %). Petrographic andchemical data indicate the presence of both tholeiitic and transitionalmagma series, with variable degree of rare earth element enrichment[(La/Nd)_n = 1–1·4 for tholeiites vs (La/Nd)_n =0·65–1 for transitional rocks]. Initial (at 88Ma) ⁸⁷Sr/⁸⁶Sr and     

Evolution of a Porphyry-Cu Mineralized Magma System at Santa Rita, New Mexico (USA)

The magmatic processes leading to porphyry-Cu mineralizationat Santa Rita are reconstructed on the basis of petrographicstudies, thermobarometry, and laser-ablation inductively-coupled-plasmamass-spectrometry analyses of silicate melt and sulfide inclusionsfrom dikes ranging from basaltic andesite to rhyodacite. Combinedresults suggest that magma evolution at Santa Rita is similarto that of sulfur-rich volcanoes situated above subduction zones,being characterized by repeated injection of hot, mafic magmainto an anhydrite-bearing magma chamber of rhyodacitic composition.The most mafic end-member identified at Santa Rita is a shoshoniticbasaltic andesite that crystallized at 1000–1050°C,1–3 kbar and log f_O2 = NNO + 0·7 to NNO + 1·0,whereas the rhyodacite crystallized at 730–760°C andlog f_O2 = NNO + 1·3 to NNO + 1·9. Mixing betweenthe two magmas caused precipitation of 0·1–0·2wt % magmatic sulfides and an associated decrease in the Cucontent of the silicate melt from 300–500 ppm to lessthan 20 ppm. Quantitative modeling suggests that temporal storageof ore-metals in magmatic sulfides does not significantly enhancethe amount of copper ultimately available to ore-forming hydrothermalfluids. Magmatic sulfides are therefore not vital to the formationof porphyry-Cu deposits, unless a mechanism is required thatholds back ore-forming metals until late in the evolution ofthe volcanic–plutonic system. KEY WORDS: porphyry-Cu; sulfur; sulfides; magma mixing; LA-ICP-MS     

The Role of Open-System Processes in the Development of Silicic Magma Chambers: a Chemical and Isotopic Investigation of the Fogo A Trachyte Deposit, Sao Miguel, Azores

The processes operating in the development of chemical zonationin silicic magma chambers have been addressed with a Sr–Nd–Pb–Hf–Thisotope study of the chemically zoned trachyte pumice depositof the Fogo A eruption, Fogo volcano, Azores. Sr isotopic variationis observed in whole rocks, glass separates and sanidine phenocrysts(whole-rock ⁸⁷Sr/⁸⁶Sr: 0·7049–0·7061; glass⁸⁷Sr/⁸⁶Sr: 0·7048–0·7052; sanidine ⁸⁷Sr/⁸⁶Sr:0·7048–0·7062). Thorium isotopic variationis observed in glass separates, with (²³⁰Th/²³²Th)_o rangingfrom 0·8737 to 0·8841, and exhibiting a negativecorrelation with Sr isotopes. The Nd, Pb and Hf isotopic compositionsof the whole-rock trachytic pumices are invariant and indistinguishablefrom basalts flanking the volcano. The Sr isotope variationsin the whole rocks are proposed to be the result of three distinctprocesses: contamination of the Fogo A magma by assimilationof radiogenic seawater-altered syenite wall rock, to explainthe Sr and Th isotopic compositions of the glass separates;incorporation of xenocrysts into the trachytic magma, requiredto explain the range in feldspar Sr isotopic compositions; andpost-eruptive surface alteration. This study emphasizes theimportance of determining the isotopic composition of glassand mineral separates rather than whole rocks when pre-eruptivemagmatic processes are being investigated. KEY WORDS: Azores; open-system processes; Sr isotopes; trachytic pumices; zoned magma chambers     

The Role of Advective Fluid Flow and Diffusion during Localized, Solid-State Dehydration: Sondrum Stenhuggeriet, Halmstad, SW Sweden

A localized dehydration zone, Söndrum stone quarry, Halmstad,SW Sweden, consists of a central, 1 m wide granitic pegmatoiddyke, on either side of which extends a 2·5–3 mwide dehydration zone (650–700°C; 800 MPa; orthopyroxene–clinopyroxene–biotite–amphibole–garnet)overprinting a local migmatized granitic gneiss (amphibole–biotite–garnet).Whole-rock chemistry indicates that dehydration of the graniticgneiss was predominantly isochemical. Exceptions include [Y+ heavy rare earth elements (HREE)], Ba, Sr, and F, which aremarkedly depleted throughout the dehydration zone. Systematictrends in the silicate and fluorapatite mineral chemistry acrossthe dehydration zone include depletion in Fe, (Y + HREE), Na,K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusionchemistry is similar in all three zones and indicates the presenceof a fluid containing CO₂, NaCl, and H₂O components. Water activitiesin the dehydration zone average 0·36, or X_H2O = 0·25.All lines of evidence suggest that the formation of the dehydrationzone was due to advective transport of a CO₂-rich fluid witha minor NaCl brine component originating from a tectonic fracture.Fluid infiltration resulted in the localized partial breakdownof biotite and amphiboles to pyroxenes releasing Ti and Ca,which were partitioned into the remaining biotite and amphibole,as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, andF. At some later stage, H₂O-rich fluids (H₂O activity >0·8)gave rise to localized partial melting and the probable injectionof a granitic melt into the tectonic fracture, which resultedin the biotite and amphibole recording a diffusion profile forF across the dehydration zone into the granitic gneiss as wellas a diffusion profile in Fe, Mn, and Mg for all Fe–Mgsilicate minerals within 100 cm of the pegmatoid dyke. KEY WORDS: charnockite; fluids; CO₂; brines; localized dehydration; Söndrum     

Records of Crustal Metasomatism in the Garnet Peridotites of the Ulten Zone (Upper Austroalpine, Eastern Alps)

Peridotites in the Ulten Zone (Upper Austroalpine, Eastern Alps),occur as small bodies within lower-crustal rocks (gneisses andmigmatites) subducted at eclogite-facies conditions during theVariscan orogeny. They record a complex metamorphic and deformationevolution as indicated by the transition from coarse-grainedspinel-bearing peridotites to fine-grained garnet + amphibole-bearingperidotites, and are interpreted as portions of mantle wedgethat were incorporated in a downgoing slab of cold continentalcrust. The transition from spinel- to garnet-bearing assemblagewas accompanied by significant input of metasomatic agents,as shown by the crystallization of abundant amphibole. Herewe present trace-element mineral chemistry data for selectedUlten peridotites, with the aim of unravelling the nature ofthe metasomatic processes. Amphiboles display significant lightrare earth element (LREE) enrichment [Ce_N/Yb_N = 3·90–11·50;LREE up to (20–50) x C1], high Sr (150–250 ppm),K (1910–7280 ppm) and Ba (280–800 ppm) contents,and low concentrations of high field strength elements (HFSE)(Zr = 14–25 ppm, Y = 6·7–16 ppm, Ti = 1150–2500ppm, Nb = 2–7 ppm). On the basis of (1) the evidence formodal orthopyroxene decrease as a result of the garnet-formingreaction rather than abundant orthopyroxene crystallization,(2) the high modal amounts of amphibole (up to 23%) in the mostmetasomatized peridotites and (3) the strong large ion lithophileelement (LILE)/HFSE fractionation in amphiboles, we infer thatthe metasomatic agent was an H₂O–CO₂ fluid with a lowCO₂/H₂O ratio. Petrological investigations and geochronologicaldata indicate that the host metapelites experienced in situpartial melting and migmatization concomitantly with the garnet+ amphibole-facies recrystallization in the enclosed peridotites.We infer that the metasomatizing hydrous fluids could representthe residual fluids left after the crystallization of leucosomes,starting from water-undersaturated melts produced during migmatizationof the host gneisses. KEY WORDS: garnet peridotite; crustal metasomatism; amphibole; hydrous fluids     

Sources and Fluids in the Mantle Wedge below Kamchatka, Evidence from Across-arc Geochemical Variation

Major and trace element and Sr–Nd–Pb isotopic variationsin mafic volcanic rocks hve been studied in a 220 km transectacross the Kamchatka arc from the Eastern Volcanic Front, overthe Central Kamchatka Depression to the Sredinny Ridge in theback-arc. Thirteen volcanoes and lava fields, from 110 to 400km above the subducted slab, were sampled. This allows us tocharacterize spatial variations and the relative amount andcomposition of the slab fluid involved in magma genesis. TypicalKamchatka arc basalts, normalized for fractionation to 6% MgO,display a strong increase in large ion lithophile, light rareearth and high field strength elements from the arc front tothe back-arc. Ba/Zr and Ce/Pb ratios, however, are nearly constantacross the arc, which suggests a similar fluid input for Baand Pb. La/Yb and Nb/Zr increase from the arc front to the back-arc.Rocks from the Central Kamchatka Depression range in ⁸⁷Sr/⁸⁶Srfrom 0·70334 to 0·70366, but have almost constantNd isotopic compositions (¹⁴³Nd/¹⁴⁴Nd 0·51307–0·51312).This correlates with the highest U/Th ratios in these rocks.Pb-isotopic ratios are mid-ocean ridge basalt (MORB)-like butdecrease slightly from the volcanic front to the back-arc. Theinitial mantle source ranged from N-MORB-like in the volcanicfront and Central Kamchatka Depression to more enriched in theback-arc. This enriched component is similar to an ocean-islandbasalt (OIB) source. Variations in (CaO)_6·0–(Na₂O)_6·0show that degree of melting decreases from the arc front tothe Central Kamchatka Depression and remains constant from thereto the Sredinny Ridge. Calculated fluid compositions have asimilar trace element pattern across the arc, although minordifferences are implied. A model is presented that quantifiesthe various mantle components (variably depleted N-MORB-mantleand enriched OIB-mantle) and the fluid compositions added tothis mantle wedge. The amount of fluid added ranges from 0·7to 2·1%. The degree of melting changes from     

Microchemical and Sr Isotopic Investigation of Zoned K-feldspar Megacrysts: Insights into the Petrogenesis of a Granitic System and Disequilibrium Crystal Growth

K-feldspar megacrysts (Kfm) are used to investigate the magmaticevolution of the 7 Ma Monte Capanne (MC) monzogranite (Elba,Italy). Dissolution and regrowth of Kfm during magma mixingor mingling events produce indented resorption surfaces associatedwith high Ba contents. Diffusion calculations demonstrate thatKfm chemical zoning is primary. Core-to-rim variations in Ba,Rb, Sr, Li and P support magma mixing (i.e. high Ba and P andlow Rb/Sr at rims), but more complex variations require othermechanisms. In particular, we show that disequilibrium growth(related to variations in diffusion rates in the melt) may haveoccurred as a result of thermal disturbance following influxof mafic magma in the magma chamber. Initial ⁸⁷Sr/⁸⁶Sr ratios(I_Sr) (obtained by microdrilling) decrease from core to rim.Inner core analyses define a mixing trend extending towardsa high I_Sr–Rb/Sr melt component, whereas the outer coresand rims display a more restricted range of I_Sr, but a largerrange of Rb/Sr. Lower I_Sr at the rim of one megacryst suggestsmixing with high-K calc-alkaline mantle-derived volcanics ofsimilar age on Capraia. Trace element and isotopic profilessuggest (1) early megacryst growth in magmas contaminated bycrust and refreshed by high I_Sr silicic melts (as seen in theinner cores) and (2) later recharge with mafic magmas (as seenin the outer cores) followed by (3) crystal fractionation, withpossible interaction with hydrothermal fluids (as seen in therim). The model is compatible with the field occurrence of maficenclaves and xenoliths. KEY WORDS: Elba; monzogranite; K-feldspar megacrysts; zoning; magma mixing; trace element; Sr isotopes; petrogenesis     

A Melt Inclusion Record of Volatiles, Trace Elements and Li-B Isotope Variations in a Single Magma System from the Plat Pays Volcanic Complex, Dominica, Lesser Antilles

Glass inclusions in plagioclase and orthopyroxene from daciticpumice of the Cabrits Dome, Plat Pays Volcanic Complex in southernDominica reveal a complexity of element behavior and Li–Bisotope variations in a single volcanic center that would gounnoticed in a whole-rock study. Inclusions and matrix glassesare high-silica rhyolite with compositions consistent with about50% fractional crystallization of the observed phenocrysts.Estimated crystallization conditions are 760–880°C,200 MPa and oxygen fugacity of FMQ + 1 to +2 log units (whereFMQ is the fayalite–magnetite–quartz buffer). Manyinclusion glasses are volatile-rich (up to 6 wt % H₂O and 2900ppm Cl), but contents range down to 1 wt % H₂O and 2000 ppmCl as a result of shallow-level degassing. Sulfur contents arelow throughout, with <350 ppm S. The trace element compositionof inclusion glasses shows enrichment in light rare earth elements(LREE; (La/Sm)_n = 2·5–6·6) and elevatedBa, Th and K contents compared with whole rocks and similaror lower Nb and heavy REE (HREE; (Gd/Yb)_n = 0·5–1·0).Lithium and boron concentrations and isotope ratios in meltinclusions are highly variable (20–60 ppm Li with ⁷Li= +4 to +15 ± 2; 60–100 ppm B with ¹¹B = +6 to+13 ± 2) and imply trapping of isotopically heterogeneous,hybrid melts. Multiple sources and processes are required toexplain these features. The mid-ocean ridge basalt (MORB)-likeHREE, Nb and Y signature reflects the parental magma(s) derivedfrom the mantle wedge. Positive Ba/Nb, B/Nb and Th/Nb correlationsin inclusion glasses indicate coupled enrichment in stronglyfluid-mobile (Ba, B) and less-mobile (Th, Nb) trace elements,which can be explained by fractional crystallization of plagioclase,orthopyroxene and Fe–Ti oxides. The ⁷Li and ¹¹B valuesare at the high end of known ranges for other island arc magmas.We attribute the high values to a ¹¹B and ⁷Li-enriched slabcomponent derived from sea-floor-altered oceanic crust and possiblyfurther enriched in heavy isotopes by dehydration fractionation.The heterogeneity of isotope ratios in the evolved, trappedmelts is attributed to shallow-level assimilation of older volcanicrocks of the Plat Pays Volcanic Complex. KEY WORDS: subduction; volcanic arcs; igneous processes; melt inclusions; SIMS; trace elements; lithium and boron isotopes; diffusion     

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

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