Calbuco Volcano and minor eruptive centers distributed along the Liquiñe-Ofqui Fault Zone,Chile (41°–42° S): contrasting origin of andesitic and basaltic magma in the Southern Volcanic Zone of the Andes

Calbuco volcano is a Late Pleistocene-Holocene composite stratovolcano located at 41°20 S, in the southern region of the Southern Volcanic Zone of the Andes (SSVZ; 37°–46° S). In contrast to basalt and basaltic andesite, which are the dominant lava types on the volcanic front from 37° to 42° S, Calbuco lavas are porphyritic andesites which contain a wide variety of crustal xenoliths. They have SiO₂ contents in the 55–60% range, and have comparatively low K₂O, Rb, Ba, Th and LREF abundances relative to other SSVZ centers. Incompatible element abundance ratios are similar to those of most SSVZ volcanics, but ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd are respectively higher and lower than those of adjacent volcanic centers. Basalts from nearby Osorno stratovolcano, 25 km to the northeast, are similar to other basaltic SSVZ volcanoes. However, basalts from several minor eruptive centers (MEC), located east of Calbuco and Osorno volcano along the Liquiñe-Ofqui fault zone (LOFZ), are enriched in Ba, Nb, Th and LREE, and have higher La/Yb and lower Ba/La, K/La and Rb/La. ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd in MEC basalts are respectively lower and higher than those of Osorno and Calbuco lavas. We suggest that MEC basalts were produced by lower extents of mantle melting than basalts from Osorno and other SSVZ stratovolcanoes, probably as a result of lower water content in the source of MEC basalts. Calbuco andesites formed from basaltic parents similar to Osorno basalts, by moderate pressure crystallization of a hornblende-bearing assemblage accompanied by crustal assimilation. Hornblende stability in the Calbuco andesites was promoted by the assimilation of hydrous metasedimentary crustal rocks, which are also an appropriate endmember for isotopic trends, together with magma storage at mid-crustal depths. The unique characteristics of Calbuco volcano, i.e. the stability of hornblende at andesitic SiO₂ contents, low ¹⁴³Nd/¹⁴⁴Nd and high ⁸⁷Sr/⁸⁶Sr, and abundant crustal xenoliths, provide evidence for crustal assimilation that is not apparent at more northerly volcanoes in the SSVZ.     

Origin of hybrid ferrolatite lavas from Magic Reservoir eruptive center,Snake River Plain,Idaho

The mineralogy and geochemical characteristics of intermediate composition ferrolatites and related lavas from the Magic Reservoir eruptive center (central Snake River Plain) have been investigated to evaluate the origin and petrologic significance of these hybrid lavas. The ferrolatites are chemically uniform, but contain a disequilibrium phenocryst/xenocryst assemblage derived in part from mixed rhyolitic and basaltic magmas that are closely represented by extrusive units in the area. The hybrid lavas also contain xenoliths of Archean granulites and have high ⁸⁷Sr/ ⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd ratios, all of which suggest significant magma-crust interaction. Quantitative models including magma mixing, minor crystal fractionation, and crustal contamination very closely reproduce the observed compositions of these ferrolatites; closed system fractionation and (or) simple bulk contamination models are not as successful and can be ruled out. It appears that preexisting mafic and silicic magmas from distinct sources (e.g., mantle and crust) encounter one another in crustal-level magma chambers under conditions where intimate mixing may occur despite wide differences in the physical properties of these liquids.     

Isotopic and trace element constraints on the petrogenesis of lavas from the Mount Adams volcanic field,Washington

Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P) _n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. δ ¹⁸O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust.     

The effect of assimilation, fractional crystallization, and ageing on U-series disequilibria in subduction zone lavas

Although most arc lavas have experienced significant magma differentiation, the effect of the differentiation process on U-series disequilibria is still poorly understood. Here we present a numerical model for simulating the effect of time-dependent magma differentiation processes on U-series disequilibria in lavas from convergent margins. Our model shows that, in a closed system with fractional crystallization, the ageing effect can decrease U-series disequilibria via radioactive decay while in an open system, both ageing and bulk assimilation of old crustal material serve to reduce the primary U-series disequilibria. In contrast, with recharge of refresh magma, significant ²²⁶Ra excess in erupted lavas can be maintained even if the average residence time is longer than 8000 years.The positive correlations of (²²⁶Ra/²³⁰Th) between Sr/Th or Ba/Th in young lavas from convergent margins have been widely used as evidence of fluid addition generating the observed ²²⁶Ra excess in subduction zones. We assess to what extent the positive correlations of (²²⁶Ra/²³⁰Th) with Sr/Th and Ba/Th observed in the Tonga arc could reflect AFC process. Results of our model show that these positive correlations can be produced during time-dependent magma differentiation at shallow crustal levels. Specifically, fractional crystallization of plagioclase and amphibole coupled with contemporaneous decay of ²²⁶Ra can produce positive correlations between (²²⁶Ra/²³⁰Th) and Sr/Th or Ba/Th (to a lesser extent). Therefore, the correlations of (²²⁶Ra/²³⁰Th) with Sr/Th and Ba/Th cannot be used to unambiguously support the fluid addition model, and the strength of previous conclusions regarding recent fluid addition and ultra-fast ascent rates of arc magmas is significantly lessened.     

Magma genesis in the New Britain island-arc: Constraints from Nd and Sr isotopes and trace-element patterns

A selected suite of fresh volcanic rocks from the New Britain island arc has been analyzed for ¹⁴³Nd/¹⁴⁴Nd, ⁸⁷Sr/⁸⁶Sr, major and trace elements to investigate relationships between isotopes, trace elements and petrology, and depth to the underlying Benioff zone. From these relationships inferences about magma generation are made utilizing Nd and Sr isotope systematics in possible source materials. Lavas ranging in composition from basalt to rhyolite show minimal variation of ¹⁴³Nd/¹⁴⁴Nd. Small variations in ⁸⁷Sr/⁸⁶Sr do not correlate with depth to the Benioff zone, but are related to magma type. Nd-Sr isotopes suggest that island arc lavas in general are derived from a mixture of suboceanic mantle and hydrothermally altered mid-ocean ridge-type basalt, but the New Britain magma source appears homogeneous with little indication of either the involvement of oceanic crust or mantle inhomogeneity. Trace element patterns in New Britain lavas are not consistent with Nd isotope data for currently accepted petrologic and trace element models of magma genesis. Mafic lavas from New Britain and other island arcs have anomalously high Sr/Nd, possibly due to components derived from subducted oceanic crust.     

Contributions of Slab Fluid, Mantle Wedge and Crust to the Origin of Quaternary Lavas in the NE Japan Arc

Quaternary lavas from the NE Japan arc show geochemical evidenceof mixing between mantle-derived basalts and crustal melts atthe magmatic front, whereas significant crustal signals arenot detected in the rear-arc lavas. The along-arc chemical variationsin lavas from the magmatic front are attributable almost entirelyto geochemical variations in the crustal melts that were mixedwith a common mantle-derived basalt. The mantle-derived basaltshave slightly enriched Sr–Pb and depleted Nd isotopiccompositions relative to the rear-arc lavas, but the variationis less pronounced if crustal contributions are eliminated.Therefore, the source mantle compositions and slab-derived fluxesare relatively uniform, both across and along the arc. Despitethis, incompatible element concentrations are significantlyhigher in the rear-arc basalts. We examine an open-system, fluid-fluxedmelting model, assuming that depleted mid-ocean ridge basalt(MORB)-source mantle melted by the addition of fluids derivedfrom subducted oceanic crust (MORB) and sediment (SED) hybridsat mixing proportions of 7% and 3% SED in the frontal- and rear-arcsources, respectively. The results reproduce the chemical variationsfound across the NE Japan arc with the conditions: 0·2%fluid flux with degree of melting F = 3% at 2 GPa in the garnetperidotite field for the rear arc, and 0·7% fluid fluxwith F = 20% at 1 GPa in the spinel peridotite field beneaththe magmatic front. The chemical process operating in the mantlewedge requires: (1) various SED–MORB hybrid slab fluidsources; (2) variable amounts of fluid; (3) a common depletedmantle source; (4) different melting parameters to explain across-arcchemical variations. KEY WORDS: arc magma; crustal melt; depleted mantle; NE Japan; Quaternary; slab fluid     

Rubidium,strontium content and strontium isotopic composition of strongly alkalic basaltic rocks from the Cape Verde islands

The Cape Verde islands are characterized by the presence of very strongly alkalic lavas. Cenozoic volcanics—covering the broadest compositional range present in the archipelago—and ranging from alkali-basalts to phonolites, associated with plutonic essexites and nepheline syenites, were analyzed for Sr isotopic compositions and concentrations in K, Rb and Sr. The close values of the Sr⁸⁷/Sr⁸⁶ ratios (ranging from 0.7029 to 0.7033) indicate a comagmatic origin for the different rock types; no correlation appears between the Sr isotopic composition and the K-content of the lavas, thus indicating that the lavas with high K₂O/K₂O + Na₂O ratio are generated from a primary magma by differentiation at shallow depths. The values of the Sr isotopic composition are distinctly lower than most values obtained for lavas of other oceanic islands. The origin of the magma type is discussed on the basis of these isotopic compositions and the K/Rb and Rb/Sr ratios: it is suggested that the primary magma has a nephelinitic composition and was formed by partial melting of a small fraction of undepleted mantle peridotite, containing phlogopite; the deeper part of the mantle where this nephelinitic magma generates would have a strontium isotopic ratio of about 0.703 and a Rb/Sr ratio lower than that of the upper part.     

Geochemical and Sr–Nd–Pb isotopic insight into the low-Ti basalts from southern Paraná Igneous Province,Brazil: the role of crustal contamination

ABSTRACT

The south hinge of the Torres Syncline in southernmost Brazil hosts a volcanic succession of pahoehoe and rubbly Gramado-type lavas belonging to the ~132 Ma Paraná–Etendeka Igneous Province. We evaluate the geochemical and Sr–Nd–Pb isotopic variations using local-scale stratigraphy in order to discuss the petrogenesis of lava flows in a single magma type and to estimate the role of crustal contamination and the potential contaminants involved. The geochemical and isotopic variations along the lava pile are not systematic, implying that the magma chamber could have undergone successive replenishments of basaltic magma. The process of crustal assimilation explains the high and widespread initial Sr isotopic ratios at 0.707798–0.715751 and the very low ε_Nd at ?8.36 to ?5.41, with associated Pb isotopic variations (18.42 < ²⁰⁶Pb/²⁰⁴Pb < 18.86; 15.65 < ²⁰⁷Pb/²⁰⁴Pb < 15.71; 38.62 < ²⁰⁸Pb/²⁰⁴Pb < 39.37). The magmatic evolution of the SCSH and LJ lava flows begins with the storage of mafic liquids during a short period in the shallow-level magma chamber, which allowed the magma ascent with composition of olivine basalts. The continuous fractional crystallization within the magma chamber coupled with variable assimilation degrees of distinct contaminants with Palaeoproterozoic and Neoproterozoic ages, in addition to significant contribution of magma recharge, led to magma ascent with basaltic andesite composition that displays at surface a simple pahoehoe morphology. The continuous magma recharge in the magma chamber coupled with higher assimilation degree allowed the formation of basaltic andesite lavas with more contaminated isotopic signatures that exhibit rubbly morphology at the surface. Differentiation process of liquids coupled with the highest assimilation degrees of distinct contaminants during longer time in a shallow-level magma chamber, which is distinct from that where SCSH and LJ magmas have been stored, led to the formation of andesites of the Morro da Cruz section that exhibit the most contaminated isotopic signatures.     

Rapid magmatic processes accompany arc–continent collision: the Western Bismarck arc, Papua New Guinea

New U–Th–Ra, major and trace element, and Sr–Nd–Pb isotope data are presented for young lavas from the New Britain and Western Bismarck arcs in Papua New Guinea. New Britain is an oceanic arc, whereas the latter is the site of an arc–continent collision. Building on a recent study of the Manus Basin, contrasts between the two arcs are used to evaluate the processes and timescales of magma generation accompanying arc–continent collision and possible slab detachment. All three suites share many attributes characteristic of arc lavas that can be ascribed to the addition of a regionally uniform subduction component derived from the subducting altered oceanic crust and sediment followed by dynamic melting of the modified mantle. However, the Western Bismarck arc lavas diverge from the Pb isotope mixing array formed by the New Britain and the Manus Basin lavas toward elevated ²⁰⁸Pb/²⁰⁴Pb. We interpret this to reflect a second and subsequent addition of sediment melt at crustal depth during collision. ²³⁸U and ²²⁶Ra excesses are preserved in all of the lavas and are greatest in the Western Bismarck arc. High-Mg andesites with high Sr/Y ratios in the westernmost arc are attributed to recent shallow mantle flux melting at the slab edge. Data for two historical rhyolites are also presented. Although these rhyolites formed in quite different tectonic settings and display different geochemical and isotopic compositions, both formed from mafic parents within millennia.     

Geochemical variations in Andean basaltic and silicic lavas from the Villarrica-Lanin volcanic chain (39.5° S): an evaluation of source heterogeneity,fractional crystallization and crustal assimilation

At 39.5° S in the southern volcanic zone of the Andes three Pleistocene-recent stratovolcanoes, Villarrica, Quetrupillan and Lanin, form a trend perpendicular to the strike of the Andes, 275 to 325 km from the Peru-Chile trench. Basalts from Villarrica and Lanin are geochemically distinct; the latter have higher incompatible element abundances and La/Sm but lower Ba/La and alkali metal/La ratios. These differences are consistent with our previously proposed models involving: a) a west to east decrease in an alkali metal-rich, high Ba/La slab-derived component which causes an across strike decrease in degree of melting; or b) a west to east increase in the contamination of subduction-related magma by enriched subcontinental lithospheric mantle. Silicic and mafic lavas from the stratovolcanoes have overlapping Sr, Nd and O isotopic ratios. Silicic lavas also have geochemical differences that parallel those of their associated basalts, e.g., rhyolite from Villarrica has lower La/Sm and incompatible element contents than high-SiO₂ andesite from Lanin. At each volcano the most silicic lavas can be modelled by closed system fractional crystallization while andesites are best explained by magma mixing. Apparently crustal contamination was not an important process in deriving the evolved lavas. Basaltic flows from small scoria cones, 20–35 km from Villarrica volcano have high incompatible element contents and low Ba/La, like Lanin basalts, but trend to higher K/Rb (356–855) and lower ⁸⁷Sr/ ⁸⁶Sr (0.70361–0.70400) than basalts from either stratovolcano. However all basalts have similar Nd, Pb and O isotope ratios. The best explanation for the unique features of the cones is that the sources of SVZ magmas, e.g., slab-derived fluids or melts of the subcontinental lithospheric mantle, have varying alkali metal and radiogenic Sr contents. These heterogeneities are not manifested in stratovolcano basalts because of extensive subcrustal pooling and mixing. This model is preferable to one involving crustal contamination because it can account for variable Sr isotope ratios and uniform Nd and Pb isotope ratios among the basalts, and the divergence of the cones from across-strike geochemical trends defined by the stratovolcanoes.     

Petrological and geochemical characteristics of Plio-Pleistocene Volcanics from Ponza Island (Tyrrhenian Sea, Italy)

Summary Volcanic rocks on Ponza Island (Tyrrhenian Sea, central Italy) consist of Pliocene submarine rhyolites and Pleistocene subaerial trachyte and comendite lavas. Chemical variations and the homogeneous Sr and Nd isotopic signatures within the analyzed Pliocene rocks are ascribed to crystal fractionation. The absolute isotopic values, however, indicate the important role of a crustal component in the origin of these magmas. The very high-silica rocks were probably derived from a superimposed mechanism which may have been connected to the ascent of hydrothermal magmatic fluids. Compositional and ⁸⁷Sr/⁸⁶Sr variations at constant ¹⁴³Nd/¹⁴⁴Nd values in the Pleistocene rocks are likely due to fractionation of the observed phenocryst assemblage, possibly coupled with minor crustal interaction. These processes, however, cannot account for the extreme enrichment of many incompatible trace elements in the comendites. Some evidence suggests the influence of a halogen- and/or CO₂-rich volatile phase. Received February 17, 2000; revised version accepted November 29, 2000     

The geochemistry and petrogenesis of the lavas of the Vulsinian District,Roman province,Central Italy

The Vulsinian lavas are dominated by a suite of undersaturated leucite-bearing basic to intermediate compositions. The remaining lavas are mainly oversaturated and have shoshonitic affinities. One hundred and thirty-five samples have been analysed for major elements and most for 20 trace elements. Twenty-seven lavas have been analysed for REE. They are all perpotassic (for the undersaturated lavas: K₂O/Na₂O=2–8) and have very high LIL element concentrations, (e.g. Rb=400–800 ppm, Th=25–150 ppm, REE/REE_cho=c.200, (LREE/HREE)_cho=c.20) even in the most basic rocks.The undersaturated lavas appear to be interrelated by fractional crystallization of cpx±olivine (from 14 to 11 wt.% CaO), cpx+leu±plg±mica (from 11 to 8 wt.% CaO), cpx+leu+plg+apa+magnetite±mica (from 8 to 5 wt.% CaO), and additional sanidine (or hyalophane)±haüyne (from 5 to 3 wt.% CaO). The saturated lavas and the few slightly undersaturated shoshonite basalts are thought to be evolved from the undersaturated magma(s) by crustal contamination or mixing with silica-rich magmas. The parental Vulsinian magma having: Mg-value=c.73, Cr=300–700 ppm, Ni=100–125 ppm, Sc= 40–50 ppm, Fo_89–92, Di_77–97 approximates a primary, mantle-derived liquid. Enrichment in LIL elements (incl. REE) and LREE/HREE suggest a small degree of partial melting from fertile mantle; whereas the low concentrations of Na, Ti and P suggest larger degrees of partial melting. This indicates that either the primary magma or the parental mantle was metasomatized by a fluid, which previously equilibrated with subducted continental material. This model agrees with published high ¹⁸O, high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd.     

Thermomechanical maturation of the continental crust and its effects on the late Eocene–early Oligocene volcanic record of the Sierra Madre del Sur Province,southern Mexico

We interpret the voluminous late Eocene–early Oligocene volcanic successions of the north-central Sierra Madre del Sur as the eruptive manifestation of a progressive thermomechanical maturation of the crust, driven by sustained igneous activity that affected the region since the early Eocene. Widespread Eocene magmatism and injection of mantle-derived melts into the crust beneath the Michoacán-Puebla area promoted the development of a hot zone extending to upper crustal levels, and the formation of a mature intracrustal magmatic system. Within this context, the intermediate siliceous compositions of the Tilzapotla, Muñeca, and Goleta explosive centres were generated through fractional crystallization, crustal contamination, and anatexis. In particular, decreasing bulk-rock Sr and Eu concentrations and Nd isotopes with increasing silica in the Tilzapotla and Muñeca suites document an evolution through low-pressure fractional crystallization of plagioclase-dominated assemblages, simultaneous with the assimilation of middle–upper crustal materials. In contrast, marked Eu, Sr, and Ba depletions coupled with high and variable Rb/Nd at constant ¹⁴³Nd/¹⁴⁴Nd in the Goleta rhyolites suggest their derivation from partial melting of biotite-bearing quartz-feldspathic lithologies. Ascent of the thermal anomaly induced by magma emplacement and accumulation at shallow depths shifted the brittle–ductile crustal transition close to the surface, and produced an ignimbrite flare-up through caldera-forming eruptions. A different petrogenetic–volcanologic scenario developed in north-western Oaxaca, where less profuse early–middle Eocene igneous activity and an ancient lower crustal basement made up of refractory granulitic lithologies inhibited the expansion of the hot zone to shallow levels, and constrained magmatic evolution at depth. Here, composite and monogenetic volcanoes with intermediate compositions were produced through high-pressure fractional crystallization and crustal contamination. Specifically, increasing La/Yb and Sm/Yb with increasing silica in the Oaxaca suite, and negative correlations of Nd isotopes with SiO₂ at low Rb/Nd, suggest garnet fractionation from parental basalts, coupled with the assimilation of Rb-depleted lower crustal materials.     

Genesis and Mixing/Mingling of Mafic and Felsic Magmas of Back-Arc Granite: Miocene Tsushima Pluton, Southwest Japan

The Middle Miocene Tsushima granite pluton is composed of leucocratic granites, gray granites and numerous mafic microgranular enclaves (MME). The granites have a metaluminous to slightly peraluminous composition and belong to the calc‐alkaline series, as do many other coeval granites of southwestern Japan, all of which formed in relation to the opening of the Sea of Japan. The Tsushima granites are unique in that they occur in the back‐arc area of the innermost Inner Zone of Southwest Japan, contain numerous miarolitic cavities, and show shallow crystallization (2–6 km deep), based on hornblende geobarometry. The leucocratic granite has higher initial ⁸⁷Sr/⁸⁶Sr ratios (0.7065–0.7085) and lower ε_Nd(t) (?7.70 to ?4.35) than the MME of basaltic–dacitic composition (0.7044–0.7061 and ?0.53 to ?5.24), whereas most gray granites have intermediate chemical and Sr–Nd isotopic compositions (0.7061–0.7072 and ?3.75 to ?6.17). Field, petrological, and geochemical data demonstrate that the Tsushima granites formed by the mingling and mixing of mafic and felsic magmas. The Sr–Nd–Pb isotope data strongly suggest that the mafic magma was derived from two mantle components with depleted mantle material and enriched mantle I (EMI) compositions, whereas the felsic magma formed by mixing of upper mantle magma of EMI composition with metabasic rocks in the overlying lower crust. Element data points deviating from the simple mixing line of the two magmas may indicate fractional crystallization of the felsic magma or chemical modification by hydrothermal fluid. The miarolitic cavities and enrichment of alkali elements in the MME suggest rapid cooling of the mingled magma accompanied by elemental transport by hydrothermal fluid. The inferred genesis of this magma–fluid system is as follows: (i) the mafic and felsic magmas were generated in the mantle and lower crust, respectively, by a large heat supply and pressure decrease under back‐arc conditions induced by mantle upwelling and crustal thinning; (ii) they mingled and crystallized rapidly at shallow depths in the upper crust without interaction during the ascent of the magmas from the middle to the upper crust, which (iii) led to fluid generation in the shallow crust. The upper mantle in southwest Japan thus has an EMI‐like composition, which plays an important role in the genesis of igneous rocks there.     

长白山区二道白河流域早更新世玄武质熔岩的成因

采用岩石化学和同位素分析方法,研究了二道白河流域早更新世玄武质熔岩的成因。玄武质熔岩由钠质拉斑玄武岩和钾质粗面玄武岩、玄武质粗面安山岩组成。它们的REE分配形式比较相近,表明它们来自共同的源区。Sr、Nd、Pb同位素示踪表明,二道白河流域早更新世玄武质熔岩岩浆源区接近于似原始地幔。它们的Mg#=100Mg O/(Mg O+Fe O)低于中国东部新生代玄武岩原始岩浆的Mg#(60~68),Ni(27.76×10-6~200.6×10-6)低于原始地幔,Rb/Sr(0.05~0.09)、Ba/Rb(15.64~264)高于原始地幔,说明这些岩石不是源自原始地幔。玄武质熔岩的DI变化于42~67,具有高Ca、高Sr、Eu正异常,微量元素图解显示玄武岩保留部分熔融趋势,粗面玄武岩、玄武质粗安岩具有结晶分异趋势,岩浆上升过程中发生了不同程度的地壳混染作用。玄武质熔岩的Nb/Ta之比为14.8~15.8,与勘察加半岛深俯冲带火山类似。Nb/Ta-(Na2O-K2O)关系图解显示研究区玄武质岩浆的形成与俯冲板片的部分熔融有关。     

Evolution of alkalic lavas at Haleakala Volcano,east Maui,Hawaii

The postshield and posterosional stages of Haleakala Volcano contain intercalated alkalic basalt and evolved alkalic lavas. Isotopic and incompatible element abundance ratios in the Haleakala postshield basalts changed systematically with time, providing evidence for significant temporal changes in the mantle components contributing to the magmatic sources. Specifically, a depleted, i.e. low⁸⁷Sr/⁸⁶Sr and high¹⁴³Nd/¹⁴⁴Nd, mantle component is more abundant in younger lavas. However, as magma-production rates decreased during the postshield and posterosional stages, basaltic melts in magma reservoirs cooled and fractionated, leading to evolved residual melts such as hawaiite. Because primary basalt compositions changed with time, the evolved Haleakala lavas formed from a range of parental compositions. However, basalts and evolved lavas of similar age and isotopic ratios (Sr and Nd) have major and trace element contents that are consistent with a crystal-fractionation model. Although alkalic basalt and hawaiite are the dominant lavas of the postshield stages of both Haleakala and Mauna Kea volcanoes, there are important differences between their lavas. For example, compositional differences between the hawaiite suites at Haleakala and Mauna Kea indicate that, on average, the evolved lavas at Haleakala formed at lower pressures. Also, at Haleakala basalts are intercalated with hawaiites, whereas at Mauna Kea basalts and hawaiites are separated by a sharp boundary. These differences probably reflect a higher magma supply rate to the Haleakala volcano.     

Geochemical trends across an arc-continent collision zone: magma sources and slab-wedge transfer processes below the Pantar Strait volcanoes, Indonesia

Four volcanoes in the Pantar Strait, the westernmost part of the extinct sector of the east Sunda arc, show remarkable across-arc variation in elemental abundances (K₂O: 1.2 to 4.3%), trace element ratios (Pb/Ce: 0.4 to 0.18; Ce/Yb: 20 to 55) and isotope ratios (¹⁴³Nd/¹⁴⁴Nd: 0.51263 to 0.51245; ⁸⁷Sr/⁸⁶Sr: 0.7053 to 0.7068; ²⁰⁶Pb/²⁰⁴Pb: 19.29 to 19.15). Pb isotopes are decoupled from Sr and Nd isotopes, with the frontal volcanoes showing the higher Nd and Pb and lower Sr isotopic ratios. The isotopic and trace element ratios of the volcanic samples are best explained by modification of a MORB-type source (with Indian Ocean island basalt-type Pb isotopic characteristics) by a fluid and a partial melt of subducted continental material (SCM). The frontal volcano contains the highest proportion of the fluid component, with a small contribution of partial melt. The source of the rear-arc volcano is strongly influenced by a partial melt of SCM that had undergone a previous dehydration event, by which it lost most of its fluid-mobile elements such as Pb. The SCM partial melt was in equilibrium with both rutile and garnet, whereas mantle melting took place in the presence of residual mica. The relatively large across-arc increase in incompatible elements can be explained by a combination of increasing addition of SCM partial melt, changing mantle wedge fertility and smaller degrees of partial melting toward the rear of the arc. Comparison with a more westerly across-arc transect shows that the relatively low ¹⁴³Nd/¹⁴⁴Nd ratios of the frontal volcano, and the decoupling of Pb from Sr and Nd isotopes are unique to the Pantar Strait volcanoes. This is likely to reflect magma generation in a collisional environment, where the leading edge of the Australian continent, rather than subducted sediment, contributes to the magma source.     

Primary melt from Sannome-gata volcano,NE Japan arc: constraints on generation conditions of rear-arc magmas

The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous ⁸⁷Sr/⁸⁶Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher ⁸⁷Sr/⁸⁶Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe²⁺)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H₂O at 1,220–1,230 °C and at ~1.8 GPa, and that the H₂O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H₂O at ~1,250 °C and at ~1.3 GPa.     

Origin of calc-alkaline series lavas at Medicine Lake Volcano by fractionation,assimilation and mixing

The results of experimental studies and examination of variations in major elements, trace elements and Sr isotopes indicate that fractionation, assimilation and magma mixing combined to produce the lavas at Medicine Lake Highland. Some characteristics of the compositional differences among the members of the calc-alkalic association (basalt-andesite-dacite-rhyolite) can be produced by fractional crystallization, and a fractionation model reproduces the major element trends. Other variations are inconsistent with a fractionation origin. Elevated incompatible element abundances (K and Rb) observed in lavas intermediate between basalt and rhyolite can be produced through assimilation of a crustal component. An accompanying increase in ⁸⁷Sr/⁸⁶Sr from ∼ 0.07030 in basalt to ∼0.7040 in rhyolite is also consistent with crustal assimilation. The compatible trace element contents (Ni and Sr) of intermediate lavas can not be produced by fractional crystallization, and suggest a magma-mixing origin for some lavas. Unusual phenocryst assemblages and textural criteria in these lavas provide additional evidence for magma mixing. A phase diagram constructed from the low pressure melting experiments identifies a distributary reaction point, where olivine+augite react to pigeonite. Parental basalts reach this point at low pressures and undergo iron-enrichment at constant SiO₂ content. The resulting liquid line of descent is characteristic of the tholeiitic trend. Calc-alkalic differentiation trends circumvent the distributary reaction point by three processes: fractionation at elevated pH₂O, assimilation and magma mixing.     

Geochemical evolution of historical lavas from Askja Volcano, Iceland: Implications for mechanisms and timescales of magmatic differentiation

The mechanisms and the timescales of magmatic evolution were investigated for historical lavas from the Askja central volcano in the Dyngjufjöll volcanic massif, Iceland, using major and trace element and Sr, Nd, and Pb isotopic data, as well as ²³⁸U-²³⁰Th-²²⁶Ra systematics. Lavas from the volcano show marked compositional variation from magnesian basalt through ferrobasalt to rhyolite. In the magnesian basalt-ferrobasalt suite (5-10 wt% MgO), consisting of lavas older than 1875 A.D., ⁸⁷Sr/⁸⁶Sr increases systematically with increasing SiO₂ content; this suite is suggested to have evolved in a magma chamber located at ∼600 MPa through assimilation and fractional crystallization. On the other hand, in the ferrobasalt-rhyolite suite (1-5 wt% MgO), including 1875 A.D. basalt and rhyolite and 20th century lavas, ⁸⁷Sr/⁸⁶Sr tends to decrease slightly with increasing SiO₂ content. It is suggested that a relatively large magma chamber occupied by ferrobasalt magma was present at ∼100 MPa beneath the Öskjuvatn caldera, and that icelandite and rhyolite magmas were produced by extraction of the less and more evolved interstitial melt, respectively, from the mushy boundary layer along the margin of the ferrobasalt magma chamber, followed by accumulation of the melt to form separate magma bodies. Ferrobasalt and icelandite lavas in the ferrobasalt-rhyolite suite have a significant radioactive disequilibrium in terms of (²²⁶Ra/²³⁰Th), and its systematic decrease with magmatic evolution is considered to reflect aging, along with assimilation and fractional crystallization processes. Using a mass-balance model in which simultaneous fractional crystallization, crustal assimilation, and radioactive decay are taken into account, the timescale for the generation of icelandite magma from ferrobasalt was constrained to be <∼3 kyr which is largely dependent on Ra crystal-melt partition coefficients we used.