The Zealandia Volcanic Complex: Further evidence of a lower crustal “hot zone” beneath the Mariana Intra‐oceanic Arc,Western Pacific

This paper addresses formation of felsic magmas in an intra‐oceanic magmatic arc. New bathymetric, petrologic, geochemical, and isotopic data for Zealandia Bank and two related volcanoes in the south‐central Mariana arc is presented and interpreted. These three volcanoes are remnants of an older andesitic volcano that evolved for some time and became dormant long enough for a carbonate platform to grow on its summit before reawakening as a rhyodacitic volcano. Zealandia lavas are transitional between low‐ and medium‐K and tholeiitic and calc‐alkaline suites. They define a bimodal suite with a gap of 56–58 wt% SiO₂; this suggests that mafic and felsic magmas have different origins. The magmatic system is powered by mantle‐derived basalts having low Zr/Y and flat rare earth element patterns. Two‐pyroxene thermometry yields equilibration temperatures of 1000–1100 °C for andesites and 900–1000 °C for dacites. Porphyritic basalts and andesites show textures expected for fractionating magmas but mostly fine‐grained felsic lavas do not. All lavas show trace element signatures expected for mantle and crustal sources that were strongly melt‐depleted and enriched by subduction‐related fluids and sediment melts. Sr and Nd isotopic compositions fall in the normal range of Mariana arc lavas. Felsic lavas show petrographic evidence of mixing with mafic magma. Zealandia Bank felsic magmatism supports the idea that a large mid‐ to lower‐crustal felsic magma body exists beneath the south‐central Mariana arc, indicating that MASH (mixing, assimilation, storage, and homogenization) zones can form beneath intra‐oceanic as well as continental arcs.     

Inverse differentiation pathway by multiple mafic magma refilling in the last magmatic activity of Nisyros Volcano, Greece

Based on detailed field, petrographic, chemical, and isotopic data, this paper shows that the youngest magmas of the active Nisyros volcano (South Aegean Arc, Greece) are an example of transition from rhyolitic to less evolved magmas by multiple refilling with mafic melts, triggering complex magma interaction processes. The final magmatic activity of Nisyros was characterized by sub-Plinian caldera-forming eruption (40?ka), emplacing the Upper Pumice (UP) rhyolitic deposits, followed by the extrusion of rhyodacitic post-caldera domes (about 31–10?ka). The latter are rich in magmatic enclaves with textural and compositional (basaltic–andesite to andesite) characteristics that reveal they are quenched portions of mafic magmas included in a cooler more evolved melt. Dome-lavas have different chemical, isotopic, and mineralogical characteristics from the enclaves. The latter have lower ⁸⁷Sr/⁸⁶Sr and higher ¹⁴³Nd/¹⁴⁴Nd values than dome-lavas. Silica contents and ⁸⁷Sr/⁸⁶Sr values decrease with time among dome-lavas and enclaves. Micro-scale mingling processes caused by enclave crumbling and by widespread mineral exchanges increase from the oldest to the youngest domes, together with enclave content. We demonstrate that the dome-lavas are multi-component magmas formed by progressive mingling/mixing processes between a rhyolitic component (post-UP) and the enclave-forming mafic magmas refilling the felsic reservoir (from 15?wt.% to 40?wt.% of mafic component with time). We recognize that only the more evolved enclave magmas contribute to this process, in which recycling of cumulate plagioclase crystals is also involved. The post-UP end-member derives by fractional crystallization from the magmas leftover after the previous UP eruptions. The enclave magma differentiation develops mainly by fractional crystallization associated with multiple mixing with mafic melts changing their composition with time. A time-related picture of the relationships between dome-lavas and relative enclaves is proposed, suggesting a delay between a mafic magma input and the relative dome outpouring. We also infer that the magma viscosity reduction by re-heating allows dome extrusion without explosive activity.     

Magma mixing in granitic rocks of the central Sierra Nevada,California

The El Capitan alaskite exposed in the North American Wall, Yosemite National Park, was intruded by two sets of mafic dikes that interacted thermally and chemically with the host alaskite. Comparisons of petrographic and compositional data for these dikes and alaskite with published data for Sierra Nevada plutons lead us to suggest that mafic magmas were important in the generation of the Sierra Nevada batholith. Specifically, we conclude that: (1) intrusion of mafic magmas in the lower crust caused partial melting and generation of alaskite (rhyolitic) magmas; (2) interaction between the mafic and felsic magmas lead to the observed linear variation diagrams for major elements; (3) most mafic inclusions in Sierra Nevada plutons represent chilled pillows of mafic magmas, related by fractional crystallization and granitoid assimilation, that dissolve into their felsic host and contaminate it to intermediate (granodioritic) compositions; (4) vesiculation of hydrous mafic magma upon chilling may allow buoyant mafic inclusions and their disaggregation products to collect beneath a pluton's domed ceiling causing the zoning (mafic margins-to-felsic core) that these plutons exhibit.     

Pre-1991 sulfur transfer between mafic injections and dacite magma in the Mt. Pinatubo reservoir

Before the 1991–1992 activity, a large andesite lava dome belonging to the penultimate Pinatubo eruptive period (Buag ∼ 500 BP) formed the volcano summit. Buag porphyritic andesite contains abundant amphibole-bearing microgranular enclaves of basaltic–andesite composition. Buag enclaves have lower K₂O and incompatible trace element (LREE, U, Th) contents than mafic pulses injected in the Pinatubo reservoir during the 1991–1992 eruptive cycle. This study shows that Buag andesite formed by mingling of a hot, water-poor and reduced mafic magma with cold, hydrous and oxidized dacite. Depending on their size, enclaves experienced variable re-equilibration during mixing/mingling. Re-equilibration resulted in hydration, oxidation and transfer of mobile elements (LILE, Cu) from the dacite to the mafic melts and prompted massive amphibole crystallization. In Buag enclaves, S-bearing phases (sulfides, apatite) and melt inclusions in amphibole and plagioclase record the evolution of sulfur partition among melt, crystal and fluid phases during magma cooling and oxidation. At high temperature, sulfur is partitioned between andesitic melt and sulfides (Ni-pyrrhotite). Magma cooling, oxidation and hydration resulted in exsolution of a S–Cl–H₂O vapor phase at the S-solubility minimum near the sulfide–sulfate redox boundary. Primary magmatic sulfide (pyrrhotite) and xenocrystic sulfide grains (pyrite), recycled together with olivines and pyroxenes from old mafic intrusives, were replaced by Cu-rich phases (chalcopyrite, cubanite) and, partially, by Ba–Sr sulfate. Sulfides degassed and transformed into residual spongy magnetite in response to fS₂ drop during final magma ascent and decompression. Our research suggests that a complete evaluation of the sulfur budget at Pinatubo must take into account the en route S assimilation from the country rocks. Moreover, this study shows that the efficiency of sulfur transfer between mafic recharges and injected magmas is controlled by the extent and rate of mingling, hydrous flushing and melt oxidation. Vigorous mixing/mingling and transformation of the magmatic recharge into a spray of small enclaves is required in order to efficiently strip their primary S-content that otherwise remains locked in the sulfides. Hydrous flushing increases the magma oxidation state of the recharges and modifies their primary volatile concentrations that cannot be recovered by the study of late-formed mineral phases and melt inclusions. Conversely, S stored in both late-formed Cu-rich sulfides and interstitial rhyolitic melt represents the pre-eruptive sulfur budget immediately available for release from mafic enclaves during their decompression.     

Magma mixing recorded in intermediate rocks associated with high-Mg andesites from the Setouchi volcanic belt, Japan: implications for Archean TTG formation

Calc-alkaline intermediate rocks are spatially and temporally associated with high-Mg andesites (HMAs, Mg#>60) in Middle Miocene Setouchi volcanic belt. The calc-alkaline rocks are characterized by higher Mg# (strongly calc-alkaline trend) than ordinary calc-alkaline rocks at equivalent silica contents. Phenocrysts in the intermediate rocks have petrographical features such as: (1) coexisting reversely and normally zoned orthopyroxene phenocrysts in single rock; (2) sieve type plagioclase in which cores are mantled by higher An%, melt inclusion-rich zone; and (3) reversely zoned amphibole phenocrysts with opacite cores. In addition, mingling textures and magmatic inclusions were observed in some rocks. These petrographic features and the mineral chemistry indicate that magma mixing was the most important process in producing the strongly calc-alkaline rocks. The core composition of normally zoned orthopyroxene phenocrysts and the mantle composition of reversely zoned orthopyroxene phenocrysts have relatively high Mg# (85–90) in maximum. Although basaltic and high-Mg andesitic magmas are candidate as possible mafic end-member magmas, basaltic magma is excluded in terms of phenocryst assemblage and bulk composition. HMA magmas are suitable mafic end-member magmas that precipitated high Mg# (90) orthopyroxene, whereas andesitic to dacitic magma are suitable felsic end-members. In contrast, it is difficult to produce the strongly calc-alkaline trend through fractional crystallization from a HMA magma, because it would require removal of plagioclase together with mafic minerals from the early stage of crystallization, whereas the precipitation of plagiolase is suppressed due to the high water content of HMA magmas. These results imply that Archean Mg#-rich TTGs (>45–55), which are an analog of the strongly calc-alkaline rocks in terms of chemistry and magma genesis, can be derived from magma mixing in which a HMA magma is the mafic end-member magma, rather than by fractional crystallization from a HMA magma.     

Remobilization of granitoid rocks through mafic recharge: evidence from basalt-trachyte mingling and hybridization in the Manori–Gorai area,Mumbai, Deccan Traps

Products of contrasting mingled magmas are widespread in volcanoes and intrusions. Subvolcanic trachyte intrusions hosting mafic enclaves crop out in the Manori–Gorai area of Mumbai in the Deccan Traps. The petrogenetic processes that produced these rocks are investigated here with field data, petrography, mineral chemistry, and whole rock major, trace, and Pb isotope chemistry. Local hybridization has occurred and has produced intermediate rocks such as a trachyandesitic dyke. Feldspar crystals have complex textures and an unusually wide range in chemical composition. Crystals from the trachytes cover the alkali feldspar compositional range and include plagioclase crystals with anorthite contents up to An₄₇. Crystals from the mafic enclaves are dominated by plagioclase An_72–90, but contain inclusions of orthoclase and other feldspars covering the entire compositional range sampled in the trachytes. Feldspars from the hybridized trachyandesitic dyke yield mineral compositions of An_80–86, An_47–54, Ab_94–99, Or_45–60, and Or_96–98, all sampled within individual phenocrysts. We show that these compositional features are consistent with partial melting of granitoid rocks by influx of mafic magmas, followed by magma mixing and hybridization of the partial melts with the mafic melts, which broadly explains the observed bulk rock major and trace element variations. However, heterogeneities in Pb isotopic compositions of trachytes are observed on the scale of individual outcrops, likely reflecting initial variations in the isotopic compositions of the involved source rocks. The combined data point to one or more shallow-level trachytic magma chambers disturbed by multiple injections of trachytic, porphyritic alkali basaltic, and variably hybridized magmas.     

Silicic magma entering a basaltic magma chamber: eruptive dynamics and magma mixing — an example from Salina (Aeolian islands,Southern Tyrrhenian Sea)

The Pollara tuff-ring resulted from two explosive eruptions whose deposits are separated by a paleosol 13 Ka old. The oldest deposits (LPP, about 0.2 km³) consist of three main fall units (A, B, C) deposited from a subplinian column whose height (7–14 km) increased with time from A to C, as a consequence of the increased magma discharge rate during the eruption (1–8x10⁶ kg/s). A highly variable juvenile population characterizes the eruption. Black, dense, highly porphyritic, mafic ejecta (SiO₂=50–55%) almost exclusively form A deposits, whereas grey, mildly vesiculated, mildly porphyritic pumice (SiO₂=56–67%) and white, highly vesiculated, nearly aphyric pumice (SiO₂=66–71%) predominate in B and C respectively. Mafic cumulates are abundant in A, while crystalline lithic ejecta first appear in B and increase upward. The LPP result from the emptying of an unusual and unstable, compositionally zoned, shallow magma chamber in which high density mafic melts capped low density salic ones. Evidence of the existence of a short crystal fractionation series is found in the mafic rocks; the andesitic pumice results from complete blending between rhyolitic and variously fractionated mafic melts (salic component up to 60 wt%), whereas bulk dacitic compositions mainly result from the presence of mafic xenocrysts within rhyolitic glasses. Viscosity and composition-mixing diagrams show that blended liquids formed when the visosities of the two end members had close values. The following model is suggested: 1. A rhyolitic magma rising through the metamorphic basement enterrd a mafic magma chamber whose souter portions were occupied by a highly viscous, mafic crystal mush. 2. Under the pressure of the rhyolitic body the nearly rigid mush was pushed upwards and mafic melts were squeezed against the walls of the chamber, beginning roof fracturing and mingling with silicic melts. 3. When the equilibrium temperature was reached between mafic and silicic melts, blended liquids rapidly formed. 4. When fractures reached the surface, the eruption began by the ejection of the mafic melts and crystal mush (A), followed by the emission of variously mingled and blended magmas (B) and ended by the ejection of nearly unmixed rhyolitic magma (C).     

Magma mingling in the ∼50 ka Rotoiti eruption from Okataina Volcanic Centre: implications for geochemical diversity and chronology of large volume rhyolites

Examination of glass and crystal chemistry in the Rotoiti Pyroclastics (>100 km³ of magma) demonstrates that compositional diversity was produced by mingling of the main rhyolite magma body with small volumes of other magmas that had been crystallizing in separate stagnant magma chambers. Most (>90%) of the Rotoiti deposits were derived from a low-K₂O, cummingtonite-bearing, rhyolitic magma (T1) discharged throughout the eruption sequence. T1 magma is homogeneous in composition (melt SiO₂=77.80±0.28 wt.%), temperature (766±13 °C) and oxygen fugacity (NNO+0.92±0.09). Most T1 phenocrysts formed in a shallow (∼200 MPa), near water-saturated (a_water=0.8) storage chamber shortly before eruption. Basaltic scoria erupted immediately before the rhyolites, and glass-bearing microdiorite inclusions within the rhyolite deposits, suggest that basalt emplaced on the floor of the chamber drove vigorous convection to produce the well-mixed T1 magma. Lithic lag breccias contain melt-bearing biotite granitoid inclusions that are compositionally distinct from T1 magma. The breccias which overlie the voluminous T1 pyroclastic flow deposits resulted from collapse of the syn-Rotoiti caldera. Post-collapse Rotoiti pumices contain T1 magma mingled with another magma (T2) that is characterized by high-K glass and biotite, and was cooler and less oxidised (712±16 °C; NNO−0.16±0.16). The mingled clasts contain bimodal disequilibrium populations of all crystal phases. The granitoid inclusions and the T2 magma are interpreted as derived from high-K magma bodies of varying ages and states of crystallization, which were adjacent to but not part of the large T1 magma body. We demonstrate that these high-K magmas contaminated the erupting T1 magma on a single pumice clast scale. This contamination could explain the reported wide range of zircon U–Th ages in Rotoiti pumices, rather than slow crystallization of a single large magma body.     

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.     

Petrological study of Nasu-Chausudake Volcano (ca. 16 ka to Present), northeastern Japan

Chausudake Volcano is representative of the active volcanoes in northeastern Japan, and has a record of many historical eruptions. Because its 16-ky eruptive history is well documented, Chausudake is well-suited for examining the temporal change of magma chamber processes and for assessing potential hazards. The activity of the Chausudake Volcano can be divided into six magmatic units (CH1-CH6). Most of its products have similar characteristics, but those from unit CH1 show wider variation. Most rocks are andesite and have plagioclase, clinopyroxene, orthopyroxene, and Fe-Ti oxides as phenocrysts, with or without olivine or quartz. Mafic inclusions, which are observed in most products, are basaltic andesites that have various combinations of the same phenocryst species. Petrographic features observed in host rocks and mafic inclusions, such as disequilibrium phenocrysts and resorbed textures, suggest magma mixing/co-mingling. Whole rock compositions of both host rocks and mafic inclusions show linear trends in variation diagrams, which suggest that the rocks are derived from the mixing/co-mingling between mafic and felsic end members. Bulk silica content of the mafic end-member magma is estimated to be ca. 52%, and contains Mg-rich olivine and An-rich plagioclase. The temperature of this end member is estimated to have been higher than 1,100 °C. Bulk silica content of the felsic end-member magma is estimated to be ~66%, and contains Mg-poor pyroxenes, An-poor plagioclase, and quartz phenocrysts, with a temperature of between 800 and 900 °C. Trace element compositions show that the end members have different origins, but have changed little over the entire 16-ky of activity. The mafic end-member magmas might come from a lower-crustal homogeneous, large magma chamber, whereas the felsic end-member magmas may be partial melts of crustal materials produced by the heat of the mafic end member. Felsic end-member magma may have accumulated in the middle crust before CH1 activity. The mixing ratio of the felsic to mafic end members was 0.5:0.5 to 0.4:0.6 for the CH1 unit, and ca. 0.4:0.6 for the other units. Considering that ca. 75% of the total volume of the eruptive products form the first unit, its wider compositional variation is attributed to more heterogeneous mixing ratios.     

Petrological variation of large-volume felsic magmas from Hakkoda-Towada caldera cluster: Implications for the origin of high-K felsic magmas in the Northeast Japan Arc

Abstract The Hakkoda‐Towada caldera cluster (HTCC) is a typical Late Cenozoic caldera cluster located in the northern part of the Northeast Japan Arc. The HTCC consists of five caldera volcanoes, active between 3.5 Ma and present time. The felsic magmas can be classified into high‐K (HK‐) type and medium‐ to low‐K (MLK‐) type based on their whole‐rock chemistry. The HK‐type magmas are characterized by higher K₂O and Rb contents and higher ⁸⁷Sr/⁸⁶Sr ratios than MLK‐type magmas. Both magmas cannot be derived from fractional crystallization of any basaltic magma in the HTCC. Assimilation‐fractional crystallization model calculations show that crustal assimilation is necessary for producing the felsic magmas, and HK‐type magmas are produced by higher degree of crustal assimilation with fractional crystallization than MLK‐type magmas. Although MLK‐type magmas were erupted throughout HTCC activity, HK‐type magmas were erupted only during the initial stage. The temporal variations of magma types suggest the large contribution of crustal components in the initial stage. A major volcanic hiatus of 3 my before the HTCC activity suggests a relatively cold crust in the initial stage. The cold crust probably promoted crustal assimilation and fractional crystallization, and caused the initial generation of HK‐type magmas. Subsequently, the repeated supply of mantle‐derived magmas raised temperature in the crust and formed relatively stable magma pathways. Such a later system produced MLK‐type magmas with lesser crustal components. The MLK‐type magmas are common and HK‐type magmas are exceptional during the Pliocene–Quaternary volcanism in the Northeast Japan Arc. This fact suggests that exceptional conditions are necessary for the production of HK‐type magmas. A relatively cold crust caused by a long volcanic hiatus (several million years) is considered as one of the probable conditions. Intensive crustal assimilation and fractional crystallization promoted by the cold crust may be necessary for the generation of highly evolved HK‐type felsic magmas.     

Genetic significance of chemical,isotopic, and petrographic features of some peralkaline salic rocks from the island of Pantelleria

An anorthoclase phenocryst separate from a pantellerite welded tuff and a slightly peralkaline nonhydrated sodatrachyte glass both have⁸⁷Sr/⁸⁶Sr ratios of0.7030 ± 0.0002. The sodatrachyte glass, withSiO₂ = 63,Al₂O₃ = 15.5,and CaO= 1.4wt%and Sr= 53ppm, is interpreted as an intermediate member in the differentiation sequence through which pantellerite melts were derived from primary mafic magmas. The very low⁸⁷Sr/⁸⁶Sr ratios, in conjunction with K/Rb ratios of 500 to 700 found for the sodatrachytes, show that the primary mafic magmas were derived from mantle material which had been depleted in incompatible elements by a much earlier episode of magma generation.     

An experimental investigation of volatile exsolution in evolving magma chambers

Previous laboratory experiments investigating the fluid dynamics of replenished magma chambers have been extended to model effects resulting from the release of gas. Turbulent transfer of heat between a layer of dense, hot and volatile-rich mafic magma overlying cooler more evolved magma can lead to crystallization and exsolution of volatiles in the lower layer. Small gas bubbles can cause the bulk density to decrease to that of the upper layer and thus produce sudden overturning and initiate mixing, followed by further exsolution of gas and explosive eruption. These processes have been modelled in the laboratory using a chemical reaction between sodium or potassium carbonate and nitric acid to release small bubbles of CO₂. We have investigated both the initial overturning produced by gas release in the lower layer, and the subsequent evolution of gas due to intimate mixing of the two layers. The latter experiments, in which the reactants remained isolated in the two layers until overturning occurred, demonstrated unambiguously that the fluxes of chemical components across the interfaces between convecting layers are very slow compared to the flux of heat. This shows that the evolution of layers of magma of different origins and composition can take place nearly independently of each other. The magmas can coexist in the same stratified chamber, until their bulk densities become equal and they mix together. The processes illustrated in these experiments could occur in H₂O-bearing magmas such as in the calcalkaline association and in CO₂-bearing mafic magmas such as in silica undersaturated suites.     

Replenishment of a mafic magma in a zoned felsic magma chamber beneath Rishiri Volcano, Japan

The trachytic Tanetomi lava from Rishiri Volcano, northern Japan, provides useful information concerning how a replenished mafic magma mixes with a compositionally zoned felsic magma in a magma chamber. The Tanetomi lava was erupted in the order of Lower lava 1 (LL1, 59.2-59.8 wt.% in SiO₂), Lower lava 2 (LL2, 58.4-59.1 wt.%), and Upper lava (UL, 59.9-65.1 wt.%). Evidence for mixing with a mafic magma is observed only in the LL2, in which a greater amount of crystals derived from the mafic magma occurs in rocks with higher SiO₂ content. The whole-rock compositional trend of the Tanetomi lavas is fairly smooth except for the LL2 lava composition, which scatter along the main composition trend. There is no reasonable composition of basaltic magma on the extrapolation of the LL2 composition trend, and the trend cannot be explained by a simple two-component magma mixing. Before the replenishment, the felsic magma was zoned in composition (58-65 wt.% in SiO₂) and temperature (1030-920°C) in the magma chamber located at the pressure of ~2 kbar. The compositional variation of the main felsic magma was produced by extraction of a fractionated interstitial melt from mush zones along the chamber walls and its subsequent mixing with the main magma (boundary layer fractionation). The LL1 magma tapped the magma chamber soon after the replenishment, before the mafic magma mixed with the overall felsic magma. Then the basalt magma mixed heterogeneously with the upper part of the felsic magma by forced convection as a fountain during injection. The mixing of the basalt magma with compositionally zoned felsic magma resulted in the characteristic composition trend of the LL2. The fraction of basaltic magma in the LL2 magma is estimated to be at most 10%. Despite such a small proportion, the basalt magma was mixed completely with the felsic magma, probably because the crystallinity of undercooled basalt magma was low enough to behave as a liquid.     

Role of precursory less-viscous mixed magma in the eruption of phenocryst-rich magma: evidence from the Hokkaido-Komagatake 1929 eruption

During the 1929 activity of Hokkaido-Komagatake volcano, the Plinian eruption of a phenocryst-rich andesite was preceded by a small eruption of more mafic magma formed by magma mixing. A similar eruption sequence has been reported for some other eruptions (Pallister et al. 1996; Venezky and Rutherford 1997), suggesting that eruption of a mixed magma is a precursor of phenocryst-rich magmas. For the purpose of understanding the tapping processes of the phenocryst-rich magma chamber, we investigated the temporal variation in the erupted magma and estimated the viscosity and density of the end-member and mixed magmas with constraints drawn from petrography. For the precursory mixed magma we estimate 33dž vol.% phenocrysts, andesitic-dacitic melt composition, 3 wt.% H₂O content, and temperature of 1040°C. In comparison, for the climactic, silicic end-member magma we estimate 48Dž vol.% phenocryst, high-silica rhyolitic melt, 3 wt.% H₂O, and temperature of 950°C, respectively. The mafic end-member magma, which was not erupted, is thought to be an almost aphyric basaltic-andesitic magma, based on mass balance calculation of the phenocryst content. The proportion of the mafic end-member magma component in the mixed magma was calculated to be 20-40 wt.%. On the basis of these data, we estimate magma viscosities of 10^3.9, 10^6.9, and 10^2.0 Pa s for the mixed, silicic end-member, and mafic end-member magmas, respectively. The calculated density differences among these magmas are inconsequential when possible errors are considered. We calculate the minimum excess pressure required for dike propagation to be 31 MPa for the silicic end-member magma and 8 MPa for the mixed magma, using the estimated viscosity and dike propagation model of Rubin (1995). If we assume that excess pressure is limited by the wall rock strength of the magma chamber, excess pressure retainable in the magma chamber is less than ca. 20 MPa. This suggests that the mixed magma was able to ascend to the surface without freezing, whereas the viscous silicic end-member magma could not. The formation and precursory eruption of the mixed magma are, therefore, effective and necessary initiation processes for the phenocryst-rich, viscous magma eruption.     

Relationships between deformation and mixing processes in lava flows: a case study from Salina (Aeolian Islands,Tyrrhenian Sea)

 The massive unit of a lava flow from Porri volcano (Salina, Aeolian Islands) displays many unusual structures related to the physical interaction between two different magmas. The magma A represents approximately 80% of the exposed lava surface; it has a crystal content of 51 vol.% and a dacitic glass composition (SiO₂=63–64 wt.%). The magma B has a basaltic-andesite glass composition (SiO₂=54–55 wt.%) and a crystal content of approximately 18 vol.%. It occurs as pillow-like enclaves, banding, boudin-like and rolling structures which are hosted in magma A. Structural analysis suggests that banding and boudin-like structures are the result of the deformation of enclaves at different shear strain. The linear correlation between strain and stratigraphic height of the measured elements indicates a single mode of deformation. We deduce that the component B deformed according to a simple shear model. Glass analyses of the A–B boundary indicate that A and B liquids mix together at high shear strain, whereas only mingling occurs at low shear strain. This suggests that the amount of deformation (i.e. forced convection) plays an important role in the formation of hybrid magmas. High shear strain may induce stretching, shearing and rolling of fluids which promote both forced convection and dynamical diffusion processes. These processes allow mixing of magmas with large differences in their physical properties. Received: 15 July 1995 / Accepted: 30 May 1996     

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.     

Lower crustal melting via magma underplating: Elemental and Sr–Nd–Pb isotopic constraints from late Mesozoic intermediate–felsic volcanic rocks in the northeastern North China Block

Ar–Ar dating, major and trace element analyses, and Sr–Nd–Pb isotope results of two groups of Lower Cretaceous (erupted at 126 and 119 Ma, respectively) intermediate–felsic lava from the northeastern North China Block (NCB) suggest their derivation from melting of mixtures between the heterogeneous lower crust and underplated basalts. Both groups exhibit high‐K calc‐alkaline to shoshonitic affinities, characterized by light rare earth element (LREE) and large ion lithophile element (LILE) enrichment and variable high field strength element (HFSE, e.g. Nb, Ta and Ti) depletion, and moderately radiogenic Sr and unradiogenic Nd and Pb isotopic compositions. Compared with Group 2, Group 1 rocks have relatively higher K₂O and Al₂O₃/(CaO + K₂O + Na₂O) in molar ratio, higher HFSE concentrations and lower Nb/Ta ratios, and higher Sr–Nd–Pb isotope ratios. Group 1 rocks were derived from a mixture of an enriched mantle‐derived magma and a lower crust that has developed radiogenic Sr and unradiogenic Nd and Pb isotopic compositions, whereas the Group 2 magmas were melts of another mixture between the same mantle‐derived component and another type of lower crust having even lower Sr, Nd, and Pb isotopic ratios. Shift in source region from Group 1 to Group 2 coincided with a change in melting conditions: hydrous melting of both the underplated basalt and the lower crust produced the earlier high‐Nb and low‐Nb/Ta melts with little or no residual Ti‐rich phases; while the younger low‐Nb and high‐Nb/Ta magmas were melted under a water‐deficient system, in which Ti‐rich phases were retained in the source. Generation of the two groups of intermediate–felsic volcanic rocks was genetically linked with the contemporaneous magma underplating event as a result of lithospheric thinning in the eastern NCB.     

Evidence for crustal assimilation by turbulently convecting,mafic alkaline magmas: Geochemistry of mantle xenolith-bearing lavas from northern Sardinia

Alkali basalt, trachybasalt and basanite magmas, containing abundant xenoliths of upper mantle origin, were erupted during the Plio-Pleistocene (2.4-0.14 Ma) in northern Sardinia. The magmas are enriched in K, Rb, Th and Ba relative to mid-ocean ridge basalts (MORB) and most ocean island basalts (OIB), resulting in high K/Nb, Th/Nb, Ba/Nb and Rb/Nb ratios. The large number of spinel peridotite inclusions in these lavas suggests that these chemical features cannot be explained by combined assimilation and fractional crystallization within the continental crust. However, volcanic rock chemistry can be explained by the assimilation of sialic rocks by turbulently convecting, mafic magmas during their ascent to the surface. Fractionation of Ba and K from the light rare earth elements (LREE) is required to explain the positive correlation of K/La and Ba/La with ⁸⁷Sr/⁸⁶Sr_(i). Consequently, bulk assimilation of crystalline basement rocks by rising, hot basaltic magmas cannot explain the observed chemical trends, and preferential melting of a low melting quartzo-feldspathic crustal component probably occurred, leaving the REE in residual phases such as apatite, zircon, sphene and amphibole. Alternatively, large ion lithophile element (LILE) enrichment may have been related to interaction of rising mafic lavas with metasomatized lithospheric mantle or enriched asthenosphere.     

Ce anomalies in Gough Island lavas — Trace element characteristics of a recycled sediment component

High precision trace element data obtained by inductively coupled plasma mass spectrometry and Sr–Nd isotope analyses are presented for mafic volcanic rocks from Gough Island, South Atlantic. The new data reveal negative Ce anomalies, with Ce/Ce^? values in Gough lavas extending down to ～ 0.92. Ce is only fractionated from other rare earth elements (REE) due to formation of Ce⁴⁺ under oxidizing conditions of near-surface environments while other REE remain trivalent. Ce anomalies in convergent margin magmas have been shown to indicate a contribution of a subducted sediment component. In contrast, Ce anomalies in intra-plate basalts have been attributed to weathering processes, but can be excluded here based on element–element systematics indicating magmatic trends rather than weathering-induced element mobility. Shallow-level contamination by local marine sediments with negative Ce anomaly inherited from seawater can be excluded because Gough lavas with increasingly negative Ce anomalies do not trend towards low Ce/Pb ratios characterizing such sediments. Rather, it is argued that the negative Ce anomalies in Gough Island lavas are consistent with variable amounts of a sediment component in the mantle plume source. Mixtures between estimates of subducting sediment columns with negative Ce anomaly and mantle capable of giving rise to Gough Island magmas without Ce anomalies reproduce the Gough compositional array with the exception of highly fluid-mobile elements. The calculated trace element composition of the deeply recycled sediment in the Gough plume source is depleted in fluid-mobile elements such as Ba and Pb relative to the composition of some present-day subducting sediments. This loss is attributed to the dehydration or flushing of sediment in the subduction factory, consistent with constraints from arc magmas.