Assessment of a shallow magmatic system: the 1888–90 eruption,Vulcano Island,Italy

The magmatic system feeding the last eruption of the volcano La Fossa, Vulcano Island, Italy was studied. The petrogenetic mechanisms controlling the differentiation of erupted rocks were investigated through petrography, mineral chemistry, major, trace and rare earth element and Sr, Nd and Pb isotopic geochemistry. In addition, melt inclusion and fluid inclusion data were collected on both juvenile material and xenolithic partially melted metamorphic clasts to quantify the P-T conditions of the magma chamber feeding the eruption. A regular and continuous chemical zoning has been highlighted: rhyolites are the first erupted products, followed by trachytes and latites, whereas rhyolitic compositions were also found in the upper part of the sequence. The chemical and isotopic composition of the rhyolites indicates that they originated by fractional crystallization from latitic magmas plus the assimilation of crustal material; the trachytes represent hybrid magmas resulting from the mixing of latites and rhyolites, contaminated in the shallow magmatic system. The erupted products, primarily compositionally zoned from latites to rhyolites, are heterogeneous due to syn-eruptive mingling. The occurrence of magmacrust interaction processes, evidenced by isotopic variations (⁸⁷Sr/⁸⁶Sr=0.70474±3 to 0.70511±3; ¹⁴³Nd/¹⁴⁴Nd=0.512550±6 to 0.512614±8; ²⁰⁶Pb/²⁰⁴Pb=19.318–19.489; ²⁰⁷Pb/²⁰⁴Pb=15.642–15.782; ²⁰⁸Pb/²⁰⁴Pb=39.175–39.613), is confirmed by the presence of partially melted metamorphic xenoliths, with ⁸⁷Sr/⁸⁶Sr=0.71633±6 to 0.72505±2 and ¹⁴³Nd/¹⁴⁴Nd=0.51229±7, in rhyolites and trachytes. AFC calculations indicate a few percentage contribution of crustal material to the differentiating magmas. Thermometric measurements on melt inclusions indicate that the crystallization temperatures of the latites and trachytes were in the range of 1050–1100° C, whereas the temperature of the rhyolites appears to have been around 1000°C at the time of the eruption. Compositional data on melt inclusions reveal that the magmas involved in the eruption contained about 1–1.5 wt.% dissolved H₂O in pre-eruptive conditions. Secondary fluid inclusions found in metamorphic xenoliths give low equilibration pressure data (30–60 MPa), giving the location of the higher portions of the chamber at around 1500–2000 m of depth.     

Sr and Nd isotope geochemistry of coexisting alkaline magma series,Cantal, Massif Central,France

Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites.⁸⁷Sr/⁸⁶Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and¹⁴³Nd/¹⁴⁴Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO₂ in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obvious crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series.The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration.     

Petrology of volcanic products younger than 42 ka on the Lipari–Vulcano complex (Aeolian Islands, Italy): an example of volcanism controlled by tectonics

Over the last 42 ka, volcanic activity at Lipari Island (Aeolian Arc, Italy) produced lava domes, flows and pyroclastic deposits with rhyolitic composition, showing in many cases evidence of magma mixing such as latitic enclaves and banding. In this same period, on nearby Vulcano Island, similar rhyolitic lava domes, pyroclastic products and lava flows, ranging in composition from shoshonite to rhyolite, were erupted. As a whole, the post-42 ka products of Lipari and Vulcano show geochemical variations with time, which are well correlated between the two islands and may correspond to a modification of the primary magmas. The rhyolitic products are similar to each other in their major elements composition, but differ in their trace element abundances (e.g. La ranging from 40 to 78 ppm for SiO₂ close to 75 wt%). Their isotopic composition is variable, too. The ⁸⁷Sr/⁸⁶Sr (0.704723–0.705992) and ¹⁴³Nd/¹⁴⁴Nd (0.512575–0.512526) ranges partially overlap those of the more mafic products (latites), having ⁸⁷Sr/⁸⁶Sr from 0.7044 to 0.7047 and ¹⁴³Nd/¹⁴⁴Nd from 0.512672 to 0.512615. ²⁰⁶Pb/²⁰⁴Pb is 19.390–19.450 in latites and 19.350–19.380 in rhyolites. Crystal fractionation and crustal assimilation processes of andesitic to latitic melts, showing an increasing content in incompatible elements in time, may explain the genesis of the different rhyolitic magmas. The rocks of the local crustal basement assimilated may correspond to lithotypes present in the Calabrian Arc. Mixing and mingling processes between latitic and rhyolitic magmas that are not genetically related occur during most of the eruptions. The alignment of vents related to the volcanic activity of the last 40 ka corresponds to the NNW–SSE Tindari–Letojanni strike-slip fault and to the correlated N–S extensional fault system. The mafic magmas erupted along these different directions display evidence of an evolution at different P_H2O conditions. This suggests that the Tindari–Letojanni fault played a relevant role in the ascent, storage and diversification of magmas during the recent volcanic activity.     

Sr–Nd isotopic and chemical characteristics of the silicic magma reservoir of the Aira pyroclastic eruption, southern Kyushu, Japan

Sr and Nd isotope and geochemical investigations were performed on a remarkably homogeneous, high-silica rhyolite magma reservoir of the Aira pyroclastic eruption (22,000 years ago), southern Kyushu, Japan. The Aira caldera was formed by this eruption with four flow units (Osumi pumice fall, Tsumaya pryoclastic flow, Kamewarizaka breccia and Ito pyroclastic flow). Quite narrow chemical compositions (e.g., 74.0–76.5 wt% of SiO₂) and Sr and Nd isotopic values (⁸⁷Sr/⁸⁶Sr=0.70584–0.70599 and _Nd=−5.62 to −4.10) were detected for silicic pumices from the four units, with the exception of minor amounts of dark pumices in the units. The high Sr isotope ratios (0.7065–0.7076) for the dark pumices clearly suggest a different origin from the silicic pumices. Andesite to basalt lavas in pre-caldera (0.37–0.93 Ma) and post-caldera (historical) eruptions show lower ⁸⁷Sr/⁸⁶Sr (0.70465–0.70540) and higher _Nd (−1.03 to +0.96) values than those of the Aira silicic and dark pumices. Both andesites of pre- and post-caldera stages are very similar in major- and trace-element characteristics and isotope ratios, suggesting that the both andesites had a same source and experienced the same process of magma generation (magma mixing between basaltic and dacitic magmas). Elemental and isotopic signatures deny direct genetic relationships between the Aira pumices and pre- and post-caldera lavas. Relatively upper levels of crust (middle–upper crust) are assumed to have been involved for magma generation for the Aira silicic and dark pumices. The Aira silicic magma was derived by partial melting of a separate crust which had homogeneous chemistry and limited isotope compositions, while the magma for the Aira dark pumice was generated by AFC mixing process between the basement sedimentary rocks and basaltic parental magma, or by partial melting of crustal materials which underlay the basement sediments. The silicic magma did not occupy an upper part of a large magma body with strong compositional zonation, but formed an independent magma body within the crust. The input and mixing of the magma for dark pumices to the base of the Aira silicic magma reservoir might trigger the eruptions in the upper part of the magma body and could produce a slight Sr isotope gradient in the reservoir. An extremely high thermal structure within the crust, which was caused by the uprise and accumulation of the basaltic magma, is presumed to have formed the large volume of silicic magma of the Aira stage.     

Sr, Nd, O and H isotopic ratios in Ascension Island lavas and plutonic inclusions; cogenetic origin

Eighteen basic rocks from Ascension Island (South Atlantic) give a mean⁸⁷Sr/⁸⁶Sr ratio of 0.70311 ± 17 for both volcanics and plutonic inclusions. The late-stage differentiated rocks (rhyolites and granitic inclusions) have much higher⁸⁷Sr/⁸⁶Sr ratios, up to 0.712. All these rocks display the same range of Nd isotopic compositions (ε_Ndvalues from6.9to11.1with a mean on12samples of8.4 ± 0.6) implying a cogenetic relation between the two sequences. The D/H systematics lead to the same conclusion.In the NdSr diagram, the data plot close to the mantle array and show a positive correlation. This suggests a mixing between a depleted MORB-type mantle, i.e. the upper mantle, and a hot-spot with less depleted geochemical characteristics, i.e. the OIB mantle source.The total range of δ¹⁸O values lies between 4.8‰ for plagioclase cumulates and 6.7‰ for the most evolved rocks (peralkaline granites and comendites). The basic rocks have values around 5.3‰, typical of mantle-derived material. These oxygen data indicate that the high⁸⁷Sr/⁸⁶Sr ratios in the most evolved rocks (both volcanic and plutonic terms) result from the combination of two different processes: incorporation of slight amounts (< 1%) of high-temperature altered oceanic crust by the magma in the late stages of the differentiation process and then in-situ Rb decay since the time of formation of these rocks. Both processes were very effective because of the high Rb and low Sr contents of these evolved rocks.Oxygen isotope systematics in the Ascension Island granites and rhyolites indicate that a fractional crystallization process alone does not produce δ¹⁸O values higher than 6.7‰, i.e. that the ultimate δ¹⁸O enrichment, relative to the initial basic magma, is not greater than 1.5‰.     

Repeated recharge,assimilation, and hybridization in magmas erupted from El Chichón as recorded by plagioclase and amphibole phenocrysts

Compositional and isotopic zoning patterns in plagioclase and amphibole phenocrysts from El Chichón record multiple cycles of country rock assimilation, magma injection, hybridization, and mixing. Laser ablation ICP-MS and electron microprobe analyses of plagioclase crystals from 7 eruptions spanning 3100 years reveal four types of zoning. These compositional and isotopic zones are often associated with textural changes observed in the crystals in thin section (e.g. sieved or patchy regions). Amphiboles are frequently zoned in Al and Si, and, in two magmas, may have clinopyroxene rims. Interestingly, most plagioclase show multiple and repeated zoning patterns. Moreover, all magmas contain all zoning patterns and textures, and crystals with substantially different sequences of zones occur within mm of one another. The most reasonable explanation for the origin of these textures is a frequently recharged chamber. Plagioclase zones with increasing anorthite contents (An) and decreasing ⁸⁷Sr/⁸⁶Sr ratios record injection by a hotter, possibly wetter, and more primitive magma (lower ⁸⁷Sr/⁸⁶Sr ratio). Zones with decreasing An and increasing ⁸⁷Sr/⁸⁶Sr ratios record assimilation of country rock and/or hybridization of the host and injected magmas; injection of hot magma may provide the heat for country rock assimilation. Changes in An without corresponding changes in ⁸⁷Sr/⁸⁶Sr ratio likely record slight variations in pressure or temperature during crystallization, or the far-field thermal effects of magma injection. Variations in ⁸⁷Sr/⁸⁶Sr ratio unaccompanied by Anzoning record assimilation of country rock. Amphibole zoning patterns also record periodic heating events; amphibole with clinopyroxene rims record episodes where the magma was heated beyond the amphibole stability field. Bulk compositional homogeneity and the juxtaposition of many crystals with disparate zoning patterns in single pumice require the magmatic system to be well mixed. Strontium diffusion rates indicate that the plagioclase zoning patterns cannot have persisted at magmatic pressures and temperatures for more than ~ 500 years, thus cycles of injection and assimilation occur on timescales equal to or shorter than the eruption recurrence interval. Long-term compositional and isotopic homogeneity indicate that there is a balance between recharge, assimilation, and crystallization.     

The southeast Australian lithospheric mantle: isotopic and geochemical constraints on its growth and evolution

Trace elements and isotopic compositions of whole rocks and mineral separates are reported for 15 spinel-bearing harzburgite and lherzolite xenoliths from southeastern Australia. These samples have an exceedingly large range in isotopic compositions, with⁸⁷Sr/⁸⁶Sr ranging from 0.70248 to 0.70834 and ε_Nd values ranging from +12.7 to −6.3. This range in isotopic compositions can be found in xenoliths from a single locality. The isotopic compositions of clinopyroxene separates and their whole rocks were found to be different in some xenoliths. Samples containing small glass pockets, which replace pre-existing hydrous minerals, generally show only small differences in isotopic composition between clinopyroxene and whole rock. In a modally metasomatized peridotite, significant differences in the Sr and Nd isotopic compositions of a coexisting phlogopite-clinopyroxene pair are present. Coexisting clinopyroxenes and orthopyroxenes from an anhydrous lherzolite have Sr isotopic compositions that are significantly different (0.70248 versus 0.70314), and yield an apparent age of 625 Ma, similar to that found previously by Dasch and Green [1]. However, the Nd isotopic compositions of the clinopyroxene and orthopyroxene are identical indicating recent (within 40 Ma) re-equilibration of Nd.Sr and Nd concentrations in the whole rocks and clinopyroxenes show an excellent positive correlation, and have an average Sr/Nd ratio of 15. This ratio is similar to the primitive mantle value, as well as that found in primitive MORBs and OIBs, but is much lower than that measured in island arc basalts and what might be predicted for a subduction zone-derived fluid. This indicates that a significant proportion of the Sr and Nd in these peridotites is introduced as a basaltic melt with intraplate chemical characteristics.The isotopic compositions of the peridotites reflect long-term, small-scale heterogeneities in the continental lithospheric mantle, and are in marked contrast to the near uniform isotopic compositions of the host alkali basalts (⁸⁷Sr/⁸⁶Sr= 0.7038–0.7041andε_Nd = +3.6 to +2.9). A minimum of three evolutionary stages are identified in the growth of the continental lithospheric mantle: an early basalt depletion event, recording the initial development and stabilization of the lithospheric mantle, followed by at least two enrichment episodes. These observations are consistent with continental lithospheric mantle growth involving the underplating of refractory peridotite diapirs.     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

Petrology of ultramafic and mafic xenoliths in picrite of Kahoolawe Island,Hawaii

A picrite lava (22 wt% MgO; 35 vol.% ol) along the western shore of the1.3–1.4 Ma Kahoolawe tholeiitic shield, Hawaii, contains small xenoliths of harzburgite, lherzolite, norite, and wehrlite. The various rock types have textures where either orthopyroxene, clinopyroxene, or plagioclase is in a poikilitic relationship with olivine. The Mg#s of the olivine, orthopyroxene, and clinopyroxene in this xenolith suite range between 86 and 82; spinel Mg#s range from 60 to 49, and plagioclase is An_75–80. A ⁸⁷Sr/⁸⁶Sr ratio for one ol-norite xenolith is 0.70444. In comparison, the host picrite has olivine phenocrysts with an average Mg# of 86.2 (range 87.5–84.5), and a whole-rock ⁸⁷Sr/⁸⁶Sr ratio of 0.70426. Textural and isotopic information together with mineral compositions indicate that the xenoliths are related to Kahoolawe tholeiitic magmatism, but are not crystallization products of the magma represented by their host picrite. Rather, the xenoliths are crystalline products of earlier primitive liquids (FeO/MgO ranging 1 to 1.3) at 5–9 kbar in the cumulate environment of a magma reservoir or conduit system. The presence of ultramafic xenoliths in picrite but not in typical Kahoolawe tholeiitic lava (6–9 wt% MgO) is consistent with replenishment of reservoirs by dense Mg-rich magma emplaced beneath resident, less dense tholeiitic magma. Mg-rich magmas have proximity to reservoir cumulate zones and are therefore more likely than fractionated residual liquids to entrain fragments of cumulate rock.     

Oxygen and strontium isotopic characteristics of calc-alkalic volcanic rocks from the central and western Japan arcs: Evaluation of contribution of crustal components to the magmas

¹⁸O/¹⁶O and ⁸⁷Sr/⁸⁶Sr ratios were determined for Quaternary calc-alkalic volcanic rocks from six volcanic rock suites in the central and western Japan arcs. The δ¹⁸O values relative to SMOW and ⁸⁷Sr/⁸⁶Sr ratios range from +6.3 to +9.9⁰/₀₀ and 0.70357 to 0.70684, respectively. Both the O- and Sr-isotopic compositions are higher than those for island-arc primitive magmas and their differentiates. The isotopic compositions of the calc-alkalic rocks cannot be derived by a simple fractional crystallization of the primitive magmas. On the other hand, the ¹⁸O- and ⁸⁷Sr-enrichment is confined to the rock suites located in well-developed island arcs having thick continental-type crust with low or negative Bouguer anomalies. Involvement of ¹⁸O- and ⁸⁷Sr-rich crustal material in the magma formation is suggested.The isotopic compositions vary remarkably within individual rock suites as well as from volcano to volcano. The data points in δ¹⁸O vs. ⁸⁷Sr/⁸⁶Sr plot accord with a mixing model between primitive magmas and crustal material of dioritic composition on an average, assuming their comparative Sr contents. The primitive magmas involved could not be low-Sr tholeiites, but magmas more or less enriched in incompatible elements including Sr, which correspond to high-alkali tholeiites or alkali basalts and their evolved magmas. The nature of the primitive magmas seems to change from tholeiitic to more alkalic with progressing island-arc evolution.Mixing of crust-derived melts is more plausible than assimilation of solid-rocks for involving 20 to 30% crustal material in the magmas along simple mixing curves. Isotopic variations between the rock suites are ascribed to variable Sr concentration radio of the end-members, variable isotopic compositions of crustal material or variable mixing ratio of the end-members. Extremely high-δ ¹⁸O rocks with moderate increase in ⁸⁷Sr/⁸⁶Sr ratio suggest another mixing process in shallower magma chambers between andesite magmas and metasedimentary rocks having high δ ¹⁸O and ⁸⁷Sr/⁸⁶Sr values but low Sr content. Subsequent fractional crystallization of once-derived magmas would be the prominent process for the rock suites showing gradual increase in ¹⁸O up to 1⁰/₀₀ with uniform ⁸⁷Sr/⁸⁶Sr ratios.     

Strontium isotopic composition and trace element data bearing on the origin of Cenozoic volcanic rocks of the central and southern Andes

The Cenozoic volcanic rocks of the southern Andes are characterized by low ⁸⁷Sr/⁸⁶Sr ratios (0.7040–0.7045), which are consistent with an origin in the downgoing slab of oceanic lithosphere or the overlying mantle. These values are distinctly lower than those from corresponding rocks of the central Andes.The calc-alkaline rocks of the central Andes exhibit higher Sr isotopic values (0.705–0.713) and variable Rb/Sr ratios. Different explanations are possible for this behaviour as well as for the positive correlation between ⁸⁷Sr/⁸⁶Sr and Rb/Sr expressed in an apparent isochron of 380 ± 50 m.y. It is postulated that these magmas result from a mixing process between a primary magma with basaltic affinities and crustal material of relatively young age.A model is proposed for the generation of the “andesitic” magmas of the central Andes by which crustal rocks of the upper part of the crust are added to the base of the crust by an accretionary process at the margin of the continent. Melts from these upper crustal rocks act as contaminants in “andesitic” magmas.The role of crustal material is still more significant in the generation of the ignimbritic magmas; they are considered to result from a two-stage melting process by which igneous rocks, belonging to a former stage of development of the Andes, are engulfed in the subduction zone, where they melt.     

Nd-Sr systematics of the Setouchi volcanic rocks,southwest Japan: a clue to the origin of orogenic andesite

Twenty-three volcanic rocks from the Setouchi volcanic belt, southwest Japan, were analyzed for Nd and Sr isotopic compositions for the purpose of examining the genetic relationships among the basalt, high-magnesium andesite (HMA) and evolved porphyritic andesite. The andesites have higher⁸⁷Sr/⁸⁶Sr (0.70487–0.70537) and lower¹⁴³Nd/¹⁴⁴Nd (0.512509–0.512731) than the basalts, i.e., 0.70408–0.70468 and 0.512691–0.512830, respectively. This result confirms earlier conclusions obtained from petrologic study that the andesites cannot be fractionation products of basaltic magma but that the andesitic and basaltic magmas were generated independently. On the basis of melting experiments for HMA and basalt, it is inferred that there is an isotopically stratified mantle beneath southwest Japan. Evolved porphyritic andesites have essentially identical Sr and Nd isotopic ratios to HMA and can be derived by fractionation of primary andesitic magma. A model to produce orogenic andesite is proposed on petrologic, experimental and isotopic bases.     

Low- and high-TiO2 flood basalts of southern Brazil: origin from picritic parentage and a common mantle source

The Serra Geral (Paraná) continental flood-basalt province of southern Brazil has two main basalt types: low-TiO₂ ( 1 wt.%) basalts occupy the southern portion, and high-TiO₂ (> 3 wt.%) basalts are largely in the northern part. Low-Ti basalts are less evolved (Mg# 60) and more radiogenic (e.g., ⁸⁷Sr/⁸⁶Sr 0.708) than high-Ti basalts (Mg# 35; ⁸⁷Sr/⁸⁶Sr 0.705). This is consistent with a model that invokes variable melting of a single mantle source to produce picritic magmas that have relatively lower and higher incompatible element contents. Varying percentages of melting can be related to varying proximity to the early Tristan da Cunha hotspot. The Mg-rich magmas fractionated 60–75% olivine, clinopyroxene, and plagioclase to yield low- or high-Ti flood basalts, assimilating more or less crust in the process. The extent of fractionation and assimilation depended on crustal “warmth” (also tied to location relative to hotspot): (1) above zones of 25% melting, warm crust relatively easily contaminated crystallizing picritic magma that originated by a high degree of melting (i.e., magma with lower incompatible element contents); additionally, high degrees of melting sustained replenishment of magma with low-Ti magma characteristics; (2) above 10% melting zones, cooler crust comparatively restricted assimilation during crystallization (of magma with higher incompatible element contents) and permitted magma evolution to high-Ti derivatives; lesser degrees of melting also limited replenishment magma and thereby allowed greater evolution of existing magma. This model refers all diagnostic geochemical and isotopic features of Serra Geral basalts to percentages of partial melting of an essentially homogeneous mantle material.     

Sr–Nd isotope ratios of gabbroic and dioritic rocks in a Cretaceous-Paleogene granite terrain, Southwest Japan

Abstract Whole‐rock chemical and Sr and Nd isotope data are presented for gabbroic and dioritic rocks from a Cretaceous‐Paleogene granitic terrain in Southwest Japan. Age data indicate that they were emplaced in the late Cretaceous during the early stages of a voluminous intermediate‐felsic magmatic episode in Southwest Japan. Although these gabbroic and dioritic rocks have similar major and trace element chemistry, they show regional variations in terms of initial Sr and Nd isotope ratios. Samples from the South Zone have high initial ⁸⁷Sr/⁸⁶Sr (0.7063–0.7076) and low initial Nd isotope ratios (?_Nd, ?2.5 to ?5.3); whereas those from the North Zone have lower initial ⁸⁷Sr/⁸⁶Sr (usually less than 0.7060) and higher Nd isotope ratios (?_Nd, ?0.8 to + 3.3). Regional variations in Sr and Nd isotope ratios are similar to those observed in granitic rocks, although gabbroic and dioritic rocks tend to have slightly lower Sr and higher Nd isotope ratios than granitic rocks in the respective zones. Limited variations in Sr and Nd isotope ratios among samples from individual zones may be attributed partly to a combination of upper crustal contamination and heterogeneity of the magma source. Contamination of magmas by upper crustal material cannot, however, explain the observed Sr and Nd isotope variations between samples from the North and South Zones. Between‐zone variations would reflect geochemical difference in magma sources. The gabbroic and dioritic rocks are enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE), showing similar normal‐type mid‐ocean ridge basalt (N‐MORB) normalized patterns to arc magmas. Geochronological and isotopic data may suggest that some gabbroic and dioritic rocks are genetically related to high magnesian andesite. Alternatively, mantle‐derived mafic or intermediate rocks which were underplated beneath the crust may be also plausible sources for gabbroic and dioritic rocks. The magma sources (the mantle wedge and lower crust) were isotopically more enriched beneath the South Zone than the North Zone during the Cretaceous‐Paleogene. Sr and Nd isotope ratios of the lower crustal source of the granitic rocks was isotopically affected by mantle‐derived magmas, resulting in similar initial Sr and Nd isotope ratios for gabbroic, dioritic and granitic rocks in each zone.     

Procida volcanic history: new insights into the evolution of the Phlegraean Volcanic District (Campania region,Italy)

New stratigraphic, major- and trace-element, and Sr-, Nd- and Pb- isotopic data on volcanic deposits older than 14 ka from the island of Procida, Italy, are presented and compared with published analyses from the rest of the Phlegraean Volcanic District (PVD). Procida rocks range in composition from basalt to shoshonite and trachyte and show ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios varying within the ranges 0.70523–0.70678, 0.512539–0.512630, 18.99–19.29, 15.67–15.69 and 39.10–39.39, respectively. The presence of a compositional gap in the range SiO₂=54–59 wt % is evidence of magma bimodality, and suggests that the feeding magmatic system was formed by at least two different reservoirs located at different depths. Geochemical and isotopic variations with increasing differentiation can be explained by fractional crystallization mechanisms, that in some cases were associated with crustal contamination that occurred in both deeper and shallower reservoirs; the most evolved magmas formed in the shallower one. Mixing/mingling processes also occurred. The variation of isotopic composition through time observed both for Procida and for Campi Flegrei and Ischia rocks is evidence of strong affinity between magmas that erupted on the entire PVD until about 40 ka. This indicates that they share a common origin and a common plumbing system. Most of the PVD eruptive centers active until about 40 ka lie within a NE-SW-oriented volcano-tectonic belt extending from the southeastern part of Ischia, through Procida and Torregaveta volcano to the northeastern sector of the present Campi Flegrei caldera. This not only indicates the existence of a link between regional structures and volcanism in the area, but also suggests that PVD magma genesis and evolution were strongly regulated by extensional tectonics. In the last 40 ka the mafic rocks erupted along this extensional structure – from Torregaveta and the islands of Ischia and Procida – indicate that it still represents an important crustal discontinuity that focuses mantle-derived magmas. Procida trachybasalts are enriched in large ion lithophile elements (LILE) and light and middle rare earth elements (LREE and MREE), and show slight negative anomalies in the high field strength elements (HFSE) relative to average MORB. A slight depletion in HREE is present. Trace element and isotope systematics can be referred to a lithospheric mantle source. The lithospheric mantle source carries intra-plate and slab-derived components, the latter probably inherited from a previous subduction event.     

Bimodal volcanism at the Katla subglacial caldera,Iceland: insight into the geochemistry and petrogenesis of rhyolitic magmas

The Katla subglacial caldera is one of the most active and hazardous volcanic centres in Iceland as revealed by its historical volcanic activity and recent seismic unrest and magma accumulation. A petrologic and geochemical study was carried out on a suite of mid-Pleistocene to Recent lavas and pyroclastic rocks originated from the caldera. The whole series is characterised by a bimodal composition, including Fe-Ti transitional alkali basalts and mildly alkalic rhyolites. Variations in trace-element composition amongst the basalts and rhyolites show that their chemical differentiation was mainly controlled by fractional crystallisation and possible assimilation. The petrology and chemistry of the few intermediate extrusive rocks show that they were derived from magma mingling or hybridisation. The absence of extrusive rocks of true intermediate magmatic composition and the occurrence of amphibole-bearing felsic xenoliths support the hypothesis of partial melting of the hydrated basalt crust as the main process leading to the generation of rhyolites. The ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr values of Katla volcanic rocks fit the general isotopic array defined by late Quaternary to Recent lavas from Iceland. A few rock specimens are distinguished by low ¹⁴³Nd/¹⁴⁴Nd values suggesting assimilation and mixing of much older crustal material. Despite their similar whole-rock chemical compositions, the postglacial rhyolitic extrusives differ from the felsic xenoliths by their glass composition and the absence of amphibole. This, together with the general chemical trend of volcanic glasses, indicates that the postglacial rhyolitic extrusives were probably derived by a process involving late reheating and partial melting of crustal material by intrusion of basaltic magmas.     

Isotope characteristics of submarine lavas from the Philippine Sea: implications for the origin of arc and basin magmas of the Philippine tectonic plate

Igneous rocks from the Philippine tectonic plate recovered on Deep Sea Drilling Project Legs 31, 58 and 59 have been analyzed for Sr, Nd and Pb isotope ratios. Samples include rocks from the West Philippine Basin, Daito Basin and Benham Rise (40–60 m.y.), the Palau-Kyushu Ridge (29–44 m.y.) and the Parece Vela and Shikoku basins (17–30 m.y.). Samples from the West Philippine, Parece Vela and Shikoku basins are MORB (mid-ocean ridge basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7026−0.7032, ¹⁴³Nd/¹⁴⁴Nd= 0.51300−0.51315, and ²⁰⁶Pb/²⁰⁴Pb= 17.8−18.1. Samples from the Daito Basin and Benham Rise are OIB (oceanic island basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7038−0.7040, ¹⁴³Nd/¹⁴⁴Nd= 0.51285−0.51291 and ²⁰⁶Pb/²⁰⁴Pb= 18.8−19.2. All of these rocks have elevated ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb compared to the Northern Hemisphere Regression Line (NHRL) and have δ²⁰⁷Pb values of 0 to +6 and δ²⁰⁸Pb values of +32 to +65. Lavas from the Palau-Kyushu Ridge, a remnant island arc, have ⁸⁷Sr/⁸⁶Sr= 7032−0.7035, ¹⁴³Nd/¹⁴⁴Nd= 0.51308−0.51310 and ²⁰⁶Pb/²⁰⁴Pb= 18.4−18.5. Unlike the basin magmas erupted before and after them, these lavas plot along the NHRL and have Pb-isotope ratios similar to modern Pacific plate MORB's. This characteristic is shared by other Palau-Kyushu Arc volcanic rocks that have been sampled from submerged and subaerial portions of the Mariana fore-arc.At least four geochemically distinct magma sources are required for these Philippine plate magmas. The basin magmas tap Source 1, a MORB-mantle source that was contaminated by EMI (enriched mantle component 1 [31]) and Source 2, an OIB-like mantle source with some characteristics of EMII (enriched mantle component 2 [31]). The arc lavas are derived from Source 3, a MORB-source or residue mantle including Sr and Pb from the subducted oceanic crust, and Source 4, MORB-source or residue mantle including a component with characteristics of HIMU (mantle component with high U/Pb [31]). These same sources can account for many of the isotopic characteristics of recent Philippine plate arc and basin lavas. The enriched components in these sources which are associated with the DUPAL anomaly were probably introduced into the asthenosphere from the deep mantle when the Philippine plate was located in the Southern Hemisphere 60 m.y.b.p.     

The Nevados de Payachata volcanic region (18°S/69°W,N. Chile)

Subduction-related volcanism in the Nevados de Payachata region of the Central Andes at 18°S comprises two temporally and geochemically distinct phases. An older period of magmatism is represented by glaciated stratocones and ignimbrite sheets of late Miocene age. The Pleistocene to Recent phase (0.3 Ma) includes the twin stratovolcanoes Volcan Pomerape and Volcan Parinacota (the Nevados de Payachata volcanic group) and two small centers to the west (i. e., Caquena and Vilacollo). Both stratovolcanoes consist of an older dome-and-flow series capped by an andesitic cone. The younger cone, i. e., V. Parinacota, suffered a postglacial cone collapse producing a widespread debris-avalanche deposit. Subsequently, the cone reformed during a brief, second volcanic episode. A number of small, relatively mafic, satellitic cinder cones and associated flows were produced during the most recent activity at V. Parinacota. At the older cone, i. e., V. Pomerape, an early dome sequence with an overlying isolated mafic spatter cone and the cone-forming andesitic-dacitic phase (mostly flows) have been recognized. The two Nevados de Payachata stratovolcanoes display continuous major- and trace-element trends from high-K₂O basaltic andesites through rhyolites (53%–76% SiO₂) that are well defined and distinct from those of the older volcanic centers. Petrography, chemical composition, and eruptive styles at V. Parinacota differ between pre- and post-debris-avalanche lavas. Precollapse flows have abundant amphibole (at SiO₂ > 59 wt%) and lower Mg numbers than postcollapse lavas, which are generally less silicic and more restricted in composition. Compositional variations indicate that the magmas of the Nevados de Payachata volcanic group evolved through a combination of fractional crystallization, crustal assimilation, and intratrend magma mixing. Isotope compositions exhibit only minor variations. Pb-isotope ratios are relatively low (²⁰⁶Pb/²⁰⁴Pb = 17.95–18.20 and²⁰⁸Pb/²⁰⁴Pb = 38.2–38.5);⁸⁷Sr/⁸⁶Sr ratios range 0.70612–0.70707,¹⁴³Nd/¹⁴⁴Nd ratios range 0.51238–0.51230, and ¹⁸O_SMOW values range from + 6.8%_o to + 7.6%_o SMOW. A comparison with other Central Volcanic Zone centers shows that the Nevados de Payachata magmas are unusually rich in Ba (up to 1800 ppm) and Sr (up to 1700 ppm) and thus represent an unusual chemical signature in the Andean arc. These chemical and isotope variations suggest a complex petrogenetic evolution involving at least three distinct components. Primary mantle-derived melts, which are similar to those generated by subduction processes throughout the Andean arc, are modified by deep crustal interactions to produce magmas that are parental to those erupted at the surface. These magmas subsequently evolve at shallower levels through assimilation-crystallization processes involving upper crust and intratrend magma mixing which in both cases were restricted to end members of low isotopic contrast.     

Compositional characteristics and geodynamic significance of late Miocene volcanic rocks associated with the Chah Zard epithermal gold–silver deposit,southwest Yazd,Iran

Whole‐rock geochemical and Sr–Nd isotopic data are presented for late Miocene volcanic rocks associated with the Chah Zard epithermal Au–Ag deposit in the Urumieh‐Dokhtar Magmatic Arc (UDMA), Iran, to investigate the magma source, petrogenesis and the geodynamic evolution of the study area. The Chah Zard andesitic to rhyolitic volcanic rocks are characterized by significant Large Ion Lithophile Element (LILE) and Light Rare Earth Element (LREE) enrichment coupled with High Field Strength Element (HFSE) depletion. Our geochemical data indicate an adakitic‐like signature for the volcanic rocks (e.g. SiO₂ > 62 wt%, Al₂O₃ > 15 wt%, MgO < 1.5 wt%, Sr/Y > 70, La/Yb > 35, Yb < 1 ppm, and Y < 18 ppm, and no significant Eu anomalies), distinguishing them from the other volcanic rocks of the UDMA. The Chah Zard volcanic rocks have similar Sr and Nd isotopic compositions; the ⁸⁷Sr/⁸⁶Sr(i) ratios range from 0.704 902 to 0.705 093 and the ε_Nd(i) values are from +2.33 to +2.70. However, the rhyolite porphyry represents the final stage of magmatism in the area and has a relatively high ⁸⁷Sr/⁸⁶Sr ratio (0.705 811). Our data suggest that the andesitic magmas are from a heterogeneous source and likely to result from partial melting of a metasomatized mantle wedge associated with a mixture of subducted oceanic crust and sediment. These melts subsequently underwent fractional crystallization along with minor amounts of crustal assimilation. Our study is consistent with the model that the volcanic host rocks to epithermal gold mineralization in the UDMA are genetically related to late Miocene Neo‐Tethyan slab break‐off beneath Central Iran.     

Petrogenesis of an 800 m lava sequence in eastern Uruguay: insights into magma chamber processes beneath the Paraná flood basalt province

Major and trace element along with representative Sr, Nd and Pb isotope data are presented for drill core samples which intersect an 800 m lava pile in eastern Uruguay. The lavas form part of the Paraná flood basalt province, are low-Ti in composition but distinct from the low-Ti Gramado magma type, and have been termed the Treinte Y Trés magma type. The lava pile overlies a large positive gravity anomaly inferred to reflect an east–west trending, mid-crustal mafic intrusive body with a calculated volume of 35,000 km³. Smooth up-section compositional variations in the basalts are interpreted to record magma evolution within this mid-crustal magma chamber. ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb increase throughout the sequence yet Mg remains relatively constant in the lower 200 m of the sequence, suggesting a role for magma chamber recharge. Above this the lavas show a regular, up-section decrease in Mg coupled with increasing ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and this is interpreted to reflect crystal fractionation combined with crustal contamination. The data provide further evidence that contamination of flood basalt magmas in crustal magma chambers is a common phenomenon and calculations suggest that the amount of crustal addition may be as high as 60–70%. Nevertheless, the effects of this crustal contamination do not appear able to account for the discrepancy between key incompatible trace element ratios and isotope ratios of the lavas and those of any putative mantle plume. In fact, La/Ta decreases with decreasing Mg and increasing ⁸⁷Sr/⁸⁶Sr indicating that the effects of crustal contamination were actually to reduce La/Ta and implying that the parental magmas had very high La/Ta (90). These constraints are clearly inconsistent with an asthenospheric origin for the parental magmas and so, consistent with mass balance calculations, it is inferred that they were derived from the lithospheric mantle.