Chlorine in submarine glasses from the Lau Basin: seawater contamination and constraints on the composition of slab-derived fluids

Measurements of chlorine concentrations in matrix glasses from 18 primitive (>6 wt% MgO) and eight evolved lavas from active spreading centers in the Lau Basin back-arc system provide insight into the processes which control chlorine concentrations in subduction-related magmas, and can be used to investigate chlorine enrichment related to fluids derived from the underlying subducted slab. Chlorine contents of the glasses are highly variable (0.008-0.835 wt%) and generally high with respect to uncontaminated mid-ocean ridge basalt. Chlorine contents are highest in fractionated lavas from propagating ridge tips and lowest in more primitive basaltic lavas. Two different styles of enrichment in chlorine (relative to other incompatible elements) are recognized. Glasses from the Central Lau Spreading and Eastern Lau Spreading Center typically have low Ba/Nb ratios indicating minimal input of slab-derived components, and high to very high ratios of chlorine relative to K₂O, H₂O, and TiO₂. This style of chlorine enrichment is highest in the most fractionated samples and is consistent with crustal assimilation of chlorine-rich altered ocean crust material. Data from the literature suggest that contamination by chlorine-rich seawater-derived components also characterizes the Woodlark Basin and North Fiji Basin back-arc systems. The second style of chlorine enrichment reflects input from slab-derived fluid(s) to the mantle wedge from the adjacent Tonga subduction zone. Basaltic glasses from the Valu Fa Ridge and Mangatolu Triple Junction show correlations between ratios of chlorine and K₂O, H₂O, and TiO₂ and indices of slab-derived fluid input such as Ba/Nb, Ba/Th and U/Th, consistent with chlorine in these lavas originating from a saline fluid added to the mantle wedge. Within the Valu Fa Ridge the measured range of chlorine contents equates to a chlorine flux of 224-1120 kg/m/yr to the back-arc crust. Using a simple melting model and additional data from other back-arc and arc sample suites we conclude that chlorine is a major component within the slab fluids that contribute to many arc and back-arc melting systems, and probably plays an important role in regulating trace element transport by slab fluids in the mantle wedge. For the back-arc suites we have examined the estimated Cl/H₂O and Cl/K₂O ratios in the slab fluid component correlate with proximity to the arc front, suggesting that progressive dehydration of the slab and/or re-equilibration and transport within the mantle wedge may influence the overall degree of chlorine enrichment within the slab fluid component. The degree of chlorine enrichment observed in most back-arc lavas also appears too great to be explained solely by melting of amphibole, phlogopite or apatite within the mantle source and suggests that chlorine must be present in another phase, possibly a chlorine-rich fluid.     

Comparison of rhyolites from continental rift,continental arc and oceanic island arc: Implication for the mechanism of silicic magma generation

We discuss the chemical compositions of rhyolites from three distinct tectonic settings: (i) the continental rift from Ethiopia (both Oligocene–Miocene and Quaternary rhyolites); (ii) the early Miocene continental arc of Japan (the Mt Wasso rhyolites related to the rifting of the Japan Sea); and (iii) the oceanic Izu–Bonin Island Arc. The comparison reveals that the oceanic island arc rhyolites have high contents of CaO, Al₂O₃, and Sr, and extremely low abundance of trace elements including K₂O. In contrast, the Ethiopian continental rift rhyolites are characterized by low contents of CaO, Al₂O₃, and Sr, and high contents of K₂O, and are enriched in the whole range of trace elements. The continental arc Mt Wasso rhyolites are apparently low in Nb content, although they display similar chemical trends to those of the Ethiopian rhyolites. This obvious difference in the chemical signatures of the rhyolites from the three tectonic settings is the consequence of their derivation from different sources. The implication of this result is that fractional crystallization processes were dominant in the rift‐related rhyolites both from continental rift and continental arc regardless of the prevailing tectonic setting and the nature of the crust (age, thickness, composition), whereas the oceanic island arc rhyolites may form through partial melting of young, mafic crust.     

Lithium isotope variations in Tonga–Kermadec arc–Lau back‐arc lavas and Deep Sea Drilling Project (DSDP) Site 204 sediments

Lithium isotopes have been identified as a promising tracer of subducted materials in arc lavas due to the observable variations in related reservoirs such as subducting sediments and altered oceanic crust. The Tonga–Kermadec arc–Lau back‐arc provides an end‐member of subduction zones with the coldest thermal structure on Earth. Reported here are Li isotope data for 14 lavas from the arc front and 7 back‐arc lavas as well as 12 pelagic and volcaniclastic sediments along a profile through the sedimentary sequence at DSDP Site 204. The arc and back‐arc lavas range from basalts to dacites in composition with SiO₂ = 48.3–65.3 wt% over which Li concentrations increase from 2 ppm to 16 ppm. Li/Y ratios range from 0.08 to 0.77 and from 0.24 to 0.65 in the arc and back‐arc lavas, respectively. The majority of the lavas have δ⁷Li that ranges from 2.5 ‰ to 5.0 ‰ with an average of (3.6 ±0.7) ‰, similar to that reported from other arcs and there is no distinction between the arc front and back‐arc lavas. The pelagic sediments have variable Li concentrations (33–133 ppm) and δ⁷Li that ranges from 1.2 ‰ to 10.2 ‰ while the volcaniclastic sediments have an even greater range of Li concentrations (3.6–165 ppm) and generally higher δ⁷Li values (8–14 ‰). However, δ⁷Li in the lavas does not correlate with commonly used trace element ratio or isotope signatures indicative of slab‐derived fluids or the sediments. This is probably because the range of δ⁷Li in the lavas and sediments overlap. Calculated sediment mass‐balance models require significantly more sediment than previous estimates based on Th–Nd–Be isotopes. This may indicate that a sizeable proportion of the total Li budget in the lavas is provided by Li‐enriched fluids from the subducting sediments and/or altered oceanic crust.     

数值模拟研究二叠纪峨眉山玄武岩浆在四川盆地的热效应

四川盆地是我国重要的含油气盆地,其西南部位于峨眉山大火成岩省的外带,二叠纪峨眉山玄武岩浆对四川盆地热历史及烃源岩热演化的影响一直备受关注.近年来,盆地古温标结果揭示出盆地在二叠纪存在高古热流（75~85 mW·m^-2）,甚至部分点位存在超高古热流（97~114 mW·m^-2）,被认为和峨眉山玄武岩浆的热效应有关.为了解这些高-超高古热流的成因机制,以及溢流到地表的玄武岩浆对二叠系及以下地层和烃源岩的热影响,本文采用二维有限元方法对二叠纪峨眉山玄武岩浆的热效应进行了模拟,得出如下结论：（1）置于岩石圈底部的地幔柱头高温异常体和挤入地壳底部的高温玄武岩浆在短期内（4 Ma内）对地表热流的扰动分别小于5 mW·m^-2和20 mW·m^-2,均无法解释四川盆地二叠纪的异常古热流.（2）古热流与侵入到地壳内部的岩浆有关,中心在7~17 km深度的不同形态的岩浆都有可能造成高或超高古热流的形成,引起超高古热流的水平状岩浆囊厚度在2~10 km,表层距地表在6~12 km之间.（3）地表岩浆越厚、下伏地层越浅,岩浆对该地层产生的热扰动越大,其中烃源岩所受影响也越大.如,上覆岩浆厚度为300 m时,在深度300 m（二叠系）、800 m（奥陶系）、1250 m（寒武系）、2000 m（震旦系）地层引起的最大升温分别是241℃、77℃、40℃和19℃,所需时间分别为2100年、6100年、1.17万年和2.56万年.（4）相变热的存在对二叠系和奥陶系地层不可忽略,如300 m厚岩浆产生的相变热可以使二叠系地层额外增温达55℃.

     

Sulfur and chlorine degassing from primitive arc magmas: temporal changes during the 1982–1983 eruptions of Galunggung (West Java, Indonesia)

The 1982–1983 eruptions of Galunggung represent a nine-month period of intermittent volcanic activity with significant changes in explosivity and emission of volatiles. Eruptions started with Vulcanian explosions but changed gradually to Strombolian activity. Compositions of juvenile material changed from basaltic andesite to high-Mg basalt, which are among the most primitive rock types known in the Indonesian arc system. Although bulk compositions suggest a single evolution trend, we infer from the compositions of melt inclusions in olivine phenocrysts that the magmas represent derivatives of a complex spectrum of primary melts. Primitive inclusions in olivine phenocrysts from magma erupted during the Strombolian phase contain up to 2000 ppm sulfur, but concentrations decrease rapidly with increasing SiO₂ down to matrix glass values (50–100 ppm). ‘Vulcanian’ inclusions appear to be degassed before eruption (200 ppm S). Chlorine concentrations increase from 750 to 2200 ppm in Strombolian, and from 800 to 1500 in Vulcanian magmas, whereas matrix glass contains about 1000 ppm in both cases. Ash leachates show two cycles of decreasing S/Cl ratios: from 9.7 to 5.6 at the start of the activity, and from 12.2 to 2.0 after four months. As the second cycle follows upon increased seismic activity at shallow depth, it probably reflects degassing of fresh sulfur-rich magma arriving in the shallow Galunggung reservoir. In contrast to the degassed state of Vulcanian magma, the significant amounts of adsorbed sulfur on the ashes point to an excess source of sulfur, which was most likely derived from intruding Strombolian magma. Hence, the observed sulfur flux of 2 Mt is not in accordance with a petrologic estimate of 0.09 Mt. Using a published value of 550 Mt of erupted material about 0.34 km³ fresh undegassed magma is needed to account for the observed sulfur flux. This is close to the erupted volume of Vulcanian magma (0.26 km³), which presumably was replaced completely by Strombolian magma during the eruption. Using the petrologic method, we calculate a total release of 0.3 Mt chlorine, which agrees well with an output of 0.47 Mt estimated independently from S/Cl ratios of the ash leachates and TOMS sulfur yields. Ash leachates show that about 35% of the sulfur and 30% of the chlorine was scavenged from the eruption plumes. Our results suggest that sulfur and chlorine were largely decoupled during degassing, which resulted in considerable variations in S/Cl ratios during the Galunggung eruptions. We infer that sulfur degassing reflects the arrival of fresh magma at shallow depth, whereas chlorine is largely derived from simultaneously erupted material. As a consequence, the petrologic estimates are more consistent with observed emissions for chlorine than for sulfur.     

A study of melt inclusions at Vulcano (Aeolian Islands, Italy): insights on the primitive magmas and on the volcanic feeding system

 This work presents the results of a microthermometric and EPMA-SIMS study of melt inclusions in phenocrysts of rocks of the shoshonitic eruptive complex of Vulcano (Aeolian Islands, Italy). Different primitive magmas related to two different evolutionary series, an older one (50–25 ka) and a younger one (15 ka to 1890 A.D.), were identified as melt inclusions in olivine Fo_88–91 crystals. Both are characterized by high Ca/Al ratio and present very similar Rb/Sr, B/Be and patterns of trace elements, with Nb and Ti anomalies typical of a subduction zone. The two basalts present the same temperature of crystallization (1180±20  °C) and similar volatile abundances. The H₂O, S and Cl contents are relatively high, whereas magmatic CO₂ concentrations are very low, probably due to CO₂ loss before low-pressure crystallization and entrapment of melt inclusions. The mineral chemistry of the basaltic assemblages and the high Ca/Al ratio of melt inclusions indicate an origin from a depleted, metasomatized clinopyroxene-rich peridotitic mantle. The younger primitive melt is characterized with respect to the older one by higher K₂O and incompatible element abundances, by lower Zr/Nb and La/Nb, and by higher Ba/Rb and LREE enrichment. A different degree of partial melting of the same source can explain the chemical differences between the two magmas. However, some anomalies in Sr, Rb and K contents suggest either a slightly different source for the two magmas or differing extents of crustal contamination. Low-pressure degassing and cooling of the basaltic magmas produce shoshonitic liquids. The melt inclusions indicate evolutionary paths via fractional crystallization, leading to trachytic compositions during the older activity and to rhyolitic compositions during the recent one. The bulk-rock compositions record a more complex history than do the melt inclusions, due to the syneruptive mixing processes commonly affecting the magmas erupted at Vulcano. The composition and temperature data on melt inclusions suggest that in the older period of activity several shallow magmatic reservoirs existed; in the younger one a relatively homogeneous feeding system is active. The shallow magmatic reservoir feeding the recent eruptive activity probably has a vertical configuration, with basaltic magma in the deeper zones and differentiated magmas in shallower, low-volume, dike-like reservoirs. Received: 11 March 1998 / Accepted: 14 July 1998     

Magma mixing in the Aleutian arc: evidence from cognate inclusions and composite xenoliths

The complexity of igneous processes in the Aleutian calc-alkaline magma series can be inferred from study of xenolithic fragments. Composite xenoliths and cognate inclusions provide direct evidence for magma—magma and wall-rock—magma mixing processes. Using distributions of Cr in clinopyroxene, compositional endmembers involved in mixing are identified within the xenoliths. The basaltic mixing endmember is more mafic than calc-alkaline lavas in the arc. Magma mixing and wall-rock assimilation within calc-alkaline basaltic to andesitic magmas is identified in phenocrystic assemblages as well as in xenoliths, and appears to be a widespread phenomenon in Aleutian calc-alkaline magmas.     

Dissecting large earthquakes in Japan: Role of arc magma and fluids

We synthesized information from recent high-resolution tomographic studies of large crustal earthquakes which occurred in the Japanese Islands during 1995–2008. Prominent anomalies of low-velocity and high Poisson's ratio are revealed in the crust and uppermost mantle beneath the mainshock hypocenters, which may reflect arc magma and fluids that are produced by a combination of subducting slab dehydration and corner flow in the mantle wedge. Distribution of 164 crustal earthquakes ( M 5.7–8.0) that occurred in Japan during 1885–2008 also shows a correlation with the distribution of low-velocity zones in the crust and uppermost mantle. A qualitative model is proposed to explain the geophysical observations recorded so far in Japan. We consider that the nucleation of a large earthquake is not entirely a mechanical process, but is closely related to the subduction dynamics and physical and chemical properties of materials in the crust and upper mantle; in particular, the arc magma and fluids.     

Element transport by dehydration of subducted sediments: Implication for arc and ocean island magmatism

High-pressure experiments on a natural pelite have been conducted at 2–11-GPa pressures in order to evaluate contributions of subducted sediments to arc and ocean island magmatism. Obtained phase relations suggest that, at least in modern subduction zones, subsolidus dehydration of chlorite and phengitic muscovite in the subducted sediments, rather than partial melting, is a predominant process in overprinting sediment components onto the magma source region. Trace element compositions of sediment-derived fluids are estimated based on dehydration experiments at 5.5 GPa and 900/1300°C. Pb is effectively transported by fluids relative to other elements. This results in the Pb enrichment for arc basalts by fluids, generated by the dehydration of subducted sediments, together with altered mid-ocean ridge basalt (MORB), and complementary depletion of Pb in subducted sediments. Inferred arc magma compositions obtained by model calculations based on the present experimental results agree well with a natural primitive arc basalt composition. A large increase in the U/Pb ratio in the subducted sediments at deeper levels than major dehydration depths results in a high Pb isotopic ratio through radioactive decay after long periods of isolation. Combined with other isotopic ratios such as Sr and Nd, it is possible to produce the EM II source, one of the enriched geochemical reservoirs for ocean island basalt magmas, by mixing of a small amount of subducted sediments with depleted or primitive mantle.     

Noble gases in submarine pillow basalt glasses from the Lau Basin: Detection of a solar component in backarc basin basalts

Noble gas elemental and isotopic abundances have been analysed in eight samples of youthful basaltic glass dredged from three different locations within the Lau Backarc Basin: (1) the King's Triple Junction, (2) the Central Lau Spreading Centre at 18°S and (3) the Eastern Lau Spreading Centre at 19°S. Samples from the Lau central and eastern spreading centres have MORB-like helium isotopic ratios of approximately 1.2 × 10⁻⁵ (8.5 R/R_A). In contrast, the samples from the King's Triple Junction yield helium isotopic ratios averaging 9.4 (±0.8) × 10⁻⁶ (6.7 ± 0.6 R/R_A), systematically lower than the MORB-like value, which may be reflecting the addition of radiogenic ⁴He released from the descending slab. Neon isotopic ratios are enriched in ²⁰Ne and ²¹Ne with respect to atmospheric ratios by as much as 23% and 62% respectively. These observations further confirm that non-atmospheric neon is a common characteristic of samples derived from the mantle. The helium and neon isotopic signatures in the samples can be explained by mixing of a primordial solar component, radiogenic and nucleogenic components produced by radioactive processes inside the Earth, and an atmospheric component. This reconnaissance survey of noble gases in a backarc basin indicates that current volcanism is dominated by magmas from the mantle wedge, a source similar to that from which MORBs are derived. The heavier noble gases (argon, krypton and xenon), however, show more atmosphere-like compositions, either indicating strong interaction of the magmas with the atmosphere or the presence of a recycled component derived from the underlying subducting slab.     

The basaltic to trachydacitic upper Diliman Tuff in Manila: Petrogenesis and comparison with deposits from Taal and Laguna Calderas

The basaltic to trachydacitic (50–65 wt.% SiO₂) upper Diliman Tuff is the youngest deposit of a sequence of tuffaceous deposits in Metro Manila. The deposit is located north of Taal Caldera and northwest of Laguna Caldera, which are both within the Southwest Luzon Volcanic Field. Chemical variations in the pumice fragments within the upper Diliman Tuff include medium-K basalt to basaltic andesite, high-K basaltic andesite to andesite and trachyandesite to trachydacite. Magma mixing/mingling is ubiquitous and is shown by banding textures in some pumice fragments, considerable range in groundmass glass composition (54 to 65 wt.% SiO₂) in a single pumice fragment, and zoning in plagioclase phenocrysts. Simple binary mixing modeling and polytopic vector analysis were used to further evaluate magma mixing. Trace-element variations are inconsistent with the medium-K and high-K magmas being related by crystal fractionation. The medium-K basalts represent hotter intrusions, which induced small degrees of partial melting in older crystallized medium-K basaltic material within the crust to produce the high-K magmas. All melts likely differentiated in the crust but the emplaced and new basaltic intrusions originated from the mantle wedge and were generated by subduction zone processes. The volcanic source vent for the upper Diliman Tuff has not been identified. In comparisons with the deposits from adjacent Taal and Laguna Calderas it is chemically distinct with respect to both major- and trace-element concentrations.     

Arc–arc collision in the Izu collision zone, central Japan, deduced from the Ashigara Basin and adjacent Tanzawa Mountains

The Pleistocene Ashigara Basin and adjacent Tanzawa Mountains, Izu collision zone, central Japan, are examined to better understand the development of an arc–arc orogeny, where the Izu–Bonin – Mariana (IBM) arc collides with the Honshu Arc. Three tectonic phases were identified based on the geohistory of the Ashigara Basin and the denudation history of the Tanzawa Mountains. In phase I, the IBM arc collided with the Honshu Arc along the Kannawa Fault. The Ashigara Basin formed as a trench basin, filled mainly by thin-bedded turbidites derived from the Tanzawa Mountains together with pyroclastics. The Ashigara Basin subsided at a rate of 1.7 mm/year, and the denudation rate of the Tanzawa Mountains was 1.1 mm/year. The onset of Ashigara Basin Formation is likely to be older than 2.2 Ma, interpreted as the onset of collision along the Kannawa Fault. Significant tectonic disruption due to the arc–arc collision took place in phase II, ranging from 1.1 to 0.7 Ma in age. The Ashigara Basin subsided abruptly (4.6 mm/year) and the accumulation rate increased to approximately 10 times that of phase I. Simultaneously, the Tanzawa Mountains were abruptly uplifted. A tremendous volume of coarse-grained detritus was provided from the Tanzawa Mountains and deposited in the Ashigara Basin as a slope-type fan delta. In phase III, 0.7–0.5 Ma, the entire Ashigara Basin was uplifted at a rate of 3.6 mm/year. This uplift was most likely caused by isostatic rebound resulting from stacking of IBM arc crust along the Kannawa Fault which is not active as the decollement fault by this time. The evolution of the Ashigara Basin and adjacent Tanzawa Mountains shows a series of the development of the arc–arc collision; from the subduction of the IBM arc beneath the Honshu Arc to the accretion of IBM arc crust onto Honshu. Arc–arc collision is not the collision between the hard crusts (massif) like a continent–continent collision, but crustal stacking of the subducting IBM arc beneath the Honshu Arc intercalated with very thick trench fill deposits.     

Melt–wall rock interaction in the mantle shown by silicate melt inclusions in peridotite xenoliths from the central Pannonian Basin (western Hungary)

In this paper we present a detailed textural and geochemical study of two equigranular textured amphibole-bearing spinel lherzolite xenoliths from Szigliget, Bakony–Balaton Highland Volcanic Field (BBHVF, western Hungary) containing abundant primary silicate melt inclusions (SMIs) in clinopyroxene rims and secondary SMIs in orthopyroxene (and rarely spinel) along healed fractures. The SMIs are dominantly composed of silicate glass and CO₂-rich bubbles. Clinopyroxene and orthopyroxene are zoned in both studied xenoliths, especially with respect to Fe, Mg, Na, and Al contents. Cores of clinopyroxenes in both xenoliths show trace element distribution close to primitive mantle. Rims of clinopyroxenes are enriched in Th, U, light rare earth elements (LREEs) and medium REEs (MREEs). Amphiboles in the Szg08 xenolith exhibit elevated Rb, Ba, Nb, Ta, LREE, and MREE contents. The composition of silicate glass in the SMIs covers a wide range from the basaltic trachyandesite and andesite to phonolitic compositions. The glasses are particularly rich in P₂O₅. Both primary and secondary SMIs are strongly enriched in incompatible trace elements (mostly U, Th, La, Zr) and display a slight negative Hf anomaly. The development of zoned pyroxenes, as well as the entrapment of primary SMIs in the clinopyroxene rims, happened after partial melting and subsequent crystallization of clinopyroxenes, most probably due to an interaction between hot volatile-bearing evolved melt and mantle wall-rocks. This silicate melt filled microfractures in orthopyroxenes (and rarely spinels) resulting in secondary SMIs.     

Metasomatized harzburgite xenoliths from Avacha volcano as fragments of mantle wedge of the Kamchatka arc: Implication for the metasomatic agent

Abstract   Abundant peridotite xenoliths have been found in pyroclasitics of Avacha (Avachinsky) volcano, the south Kamchatka arc, Russia. They are mostly refractory harzburgite with or without clinopyroxene: the Fo of olivine and Cr/(Cr + Al) atomic ratio of spinel range from 91 to 92 and from 0.5 to 0.7, respectively. They are metasomatized to various extents, and the metasomatic orthopyroxene has been formed at the expense of olivine. The metasomatic orthopyroxene, free of deformation and exsolution, is characterized by low contents of CaO and Cr₂O₃. The complicated way of replacement possibly indicates low viscosity of the metasomatic agent, namely hydrous fluids released from the relatively cool slab beneath the south Kamchatka arc. This is a good contrast to the north Kamchatka arc, where the slab has been hot enough to provide slab-derived melts. High content of total orthopyroxene, 40 vol% on average, in metasomatized harzburgite from Avacha suggests silica enrichment of the mantle wedge, and is equivalent to some subcratonic harzburgite. Some subcratonic harzburgites therefore could have been formed by transportation of subarc metasomatized peridotites to a deeper part of the upper mantle.     

Determination of pre-eruptive H2O,F and Cl contents of silicic magmas using melt inclusions: Examples from Taupo volcanic center,New Zealand

Water, F, and Cl contents of melt inclusions in phenocrysts from the 2-ka-old Taupo and Hatepe plinian tephras, and the 22-ka-old Okaia tephra from the Taupo volcanic center, New Zealand, were measured by electron and ion microprobe. Major and trace element chemistry of the inclusions is similar to that of bulk rock, supporting our assumption that volatile contents of inclusions are representative of the magma in which the crystals grew. Inclusions in the 2-ka Taupo plinian tephra contain a mean of 4.3 wt% H₂O, 450 ppm F, and 1700 ppm Cl; from the Hatepe plinian tephra 4.3 wt% H₂O, 430 ppm F, and 1700 ppm Cl; and from the Okaia tephra 5.9 wt% H₂O, 470 ppm F, and 2100 ppm Cl. Sulfur was below the detection limit of 200 ppm. The constant H₂O, F and Cl from a number of stratigraphic horizons in the tephra deposits suggest that the Taupo and Hatepe plinian tephras (>8.2 km³ magma volume) were derived from a magma body that did not contain a strong volatile gradient. By inference, there is no pre-eruptive volatile difference between these plinian eruptions and a phrea-toplinian eruption which occurred between the two. Virtually no major element zonation is seen in this eruptive sequence. Although the Okaia tephra was also erupted from the Taupo volcanic center, probably from a similar vent area, its higher volatile contents and distinct composition as compared to the Taupo tephras show that it was derived from a different, and possibly deeper, magma body.     

Across-arc geochemical variation of Quaternary lavas in West Java, Indonesia: Mass-balance elucidation using arc basalt simulator model

The Sunda Arc of Indonesia developed along the convergent margin between the Eurasian and the Australian Plates. More than 100 Quaternary volcanic centers occur along the arc. The West Java Arc is a segment of the Sunda Arc in which more than 10 volcanic centers are located, corresponding to the 120 to 200 km depth contours of the Wadati–Benioff zone. The geochemistry of 207 Quaternary lavas from six centers across the arc was investigated. The lavas range from basalt to dacite. Incompatible element abundances increase from the volcanic front to the rear‐arc in response to a change from low‐K to high‐K suites. Nd–Sr isotope compositions of the basalts scatter between mid‐ocean ridge basalt (MORB) source mantle and Indian Ocean sediment (SED) compositions, with volcanic front low‐K basalts having more radiogenic Nd than the rear‐arc basalts. It is suggested that mixing between slab‐derived fluids mainly from the SED and melt from MORB source mantle played a significant role in determining the geochemistry of the West Java basalts. Incompatible element patterns in primitive mantle normalized multi‐element plots are almost identical across the arc, except for greater inclination and weaker positive Sr spikes in the rear‐arc basalts. This suggests a lower degree of partial melting in the rear‐arc mantle, accompanied by change in SED fluid composition between the volcanic front and the rear‐arc. The latter is confirmed by fluid‐fluxed melting model calculations using multiple trace elements and Nd and Sr isotopes. All the West Java Arc lavas require deficit of Sr from the slab SED. This may occur due to selective breakdown of Sr‐rich hydrous silicate minerals, such as zoisite, at shallower depths before the SED component reaches the depth of dehydration effective for magma genesis. The rear‐arc basalts need further Sr deficits along with lesser fluid. These features are commonly observed in many arc basalts, and are likely attributable to the same mechanism.     

Mafic and ultramafic xenoliths in San Bartolo lava field: New insights on the ascent and storage of Stromboli magmas

Mafic and ultramafic xenoliths are well represented within a large basaltic lava field of Stromboli. These basalts, known as San Bartolo lavas, show a high-K calc-alkaline (HKCA) affinity and were erupted <5 ka BP. Xenoliths consist of olivin-gabbro, gabbronorite, anorthosite, dunite, wehrlite and clinopyroxenite. Thermobarometric estimates for the crystallization of gabbroic materials show minima equilibration pressures of 0.17–0.24 GPa, at temperatures ranging from 940 to 1,030°C. These materials interacted with hydrous ascending HKCA basaltic magmas (with temperatures of 1,050–1,100°C) at pressures of about 0.2–0.4 GPa. These pressure regimes are nearly identical to those found for the crystallization of phenocrystic phases within HKCA basaltic lavas. Gabbroic inclusions are regarded as cumulates and represent crystallized portions of earlier HKCA Strombolian basalts.Dunite and wehrlite show porphyroclastic-heterogranular textures, whereas the clinopyroxenite exhibit a mosaic-equigranular texture typical of mantle peridotites. These ultramafic materials are in equilibrium with more primitive basaltic magmas (under moderately hydrous and anhydrous conditions) at pressures of 0.8–1.2 GPa, which is below the crust-mantle transition, located at about 20 km depth under Stromboli.Major and trace element distributions indicate comagmatism between the host basaltic lava and the mafic and ultramafic inclusions. REE patterns for mafic nodules are relatively regular and overlap the field of basaltic lavas (HKCA). They show moderate to high LREE enrichments and moderate enrichments in HREE relative to chonrites. Spider diagrams also show significant similarities between the lavas and the mafic-ultramafic xenoliths as well.During their ascent, primitive Strombolian magmas may be stored in upper-mantle regions where they interact with peridotitic materials and partly differentiate (to give dunite and wehrlite) before migrating to upper crustal levels. In this region, hydrous basaltic magmas (with estimated water contents of 2–3.5 wt%) are stored in the subvolcanic environment, and are allowed to crystallize the gabbroic materials before reaching the surface under nearly anhydrous conditions.An erratum to this article can be found at     

Domains and enrichment mechanism of the lithospheric mantle in western Yunnan: A comparative study on two types of Cenozoic ultrapotassic rocks

West Yunnan is made of the Yangtze Craton, theSouth China Block, the Indochina Block and severalother micro-terranes formed at different times. It iscross-cut by the NW-SE-trending Ailao Shan-RedRiver (ASRR) fault, which runs over 1000 km fromthe eastern margin of the Qinghai-Tibet Plateau,through Vietnam and to the North Gulf (fig. 1). TheASRR fault is an important geological and topog-raphic boundary in East Asia. The sinistral movementof the Indochina Block along this fault ev…     

Magma degassing and basaltic eruption styles: a case study of 2000 year BP Xitle volcano in central Mexico

To investigate the relationship between volatile abundances and eruption style, we have analyzed major element and volatile (H₂O, CO₂, S) concentrations in olivine-hosted melt inclusions in tephra from the 2000 yr BP eruption of Xitle volcano in the central Trans-Mexican Volcanic Belt. The Xitle eruption was dominantly effusive, with fluid lava flows accounting for 95% of the total dense rock erupted material (1.1 km³). However, in addition to the initial, Strombolian, cinder cone-building phase, there was a later explosive phase that interrupted effusive activity and deposited three widespread ash fall layers. Major element compositions of olivine-hosted melt inclusions from these ash layers range from 52 to 58 wt.% SiO₂, and olivine host compositions are Fo_84–86. Water concentrations in the melt inclusions are variable (0.2–1.3 wt.% H₂O), with an average of 0.45±0.3 (1σ) wt.% H₂O. Sulfur concentrations vary from below detection (50 ppm) to 1000 ppm but are mostly ≤200 ppm and show little correlation with H₂O. Only the two inclusions with the highest H₂O have detectable CO₂ (310–340 ppm), indicating inclusion entrapment at higher pressures (700–900 bars) than for the other inclusions (≤80 bars). The low and variable H₂O and S contents of melt inclusions combined with the absence of less soluble CO₂ indicates shallow-level degassing before olivine crystallization and melt inclusion formation. Olivine morphologies are consistent with the interpretation that most crystallization occurred rapidly during near-surface H₂O loss. During cinder cone eruptions, the switch from initial explosive activity to effusive eruption probably occurs when the ascent velocity of magma becomes slow enough to allow near-complete degassing of magma at shallow depths within the cone as a result of buoyantly rising gas bubbles. This allows degassed lavas to flow laterally and exit near the base of the cone while gas escapes through bubbly magma in the uppermost part of the conduit just below the crater. The major element compositions of melt inclusions at Xitle show that the short-lived phase of renewed explosive activity was triggered by a magma recharge event, which could have increased overpressure in the storage reservoir beneath Xitle, leading to increased ascent velocities and decreased time available for degassing during ascent.     

Propagation of P and S-waves in magmas with different crystal contents: Insights into the crystallinity of magmatic reservoirs

Increasing amount of crystals tends to reduce the mobility of magmas and modifies its elastic characteristics (e.g. [Caricchi, L. et al., 2007. Non-Newtonian rheology of crystal-bearing magmas and implications for magma ascent dynamics. Earth and Planetary Science Letters, 264: 402–419.; Bagdassarov, N., Dingwell, D.B. and Webb, S.L., 1994. Viscoelasticity of crystal- and bubble-bearing rhyolite melts. Physics of the Earth and Planetary Interior, 83: 83–99.]). To quantify the effect of crystals on the elastic properties of magmas the propagation speed of shear and compressional waves have been measured at pressure and temperatures relevant for natural magmatic reservoirs. The measurements have been performed in aggregates at variable particle fractions (? = 0–0.7). The measurements were carried out at 200 MPa confining pressure and temperatures between 300 K and 1273 K (i.e. across the glass transition temperature (Tg) from glass to melt). The specimens were mixtures of a haplogranitic melt containing 5.25 wt.% H₂O and variable amounts of sub-spherical alumina particles. Additional experiments were carried out on a sample containing both, crystals and air bubbles. The temperature derivatives of the shear (dVs/dT) and compressional wave (dVp/dT) velocities for pure glass and samples with a crystal fraction of 0.5 are different below and above the glass transition temperature. For a crystal fraction 0.7, only dVp/dT changed above the Tg. In the presence of gas bubbles, Vp and Vs decrease constantly with increasing temperature. The bubble-bearing material yields a lower bulk modulus relative to its shear modulus. The propagation velocities of compressional and shear waves increase non-linearly with increasing crystal fraction with a prominent raise in the range 0.5 < ? < 0.7. The speed variations are only marginally related to the density increase due to the presence of crystals, but are dominantly related to the achievement of a continuous crystal framework. The experimental data set presented here can be utilized to estimate the relative proportions of crystals and melt present in a magmatic reservoir, which, in turn, is one of the fundamental parameters determining the mobility of magma and, consequently, exerting a prime control on the likelihood of an eruption from a sub-surficial magma reservoir.