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Recent diving with the JAMSTEC Shinkai 6500 manned submersible in the Mariana fore arc southeast of Guam has discovered that MORB‐like tholeiitic basalts crop out over large areas. These “fore‐arc basalts” (FAB) underlie boninites and overlie diabasic and gabbroic rocks. Potential origins include eruption at a spreading center before subduction began or eruption during near‐trench spreading after subduction began. FAB trace element patterns are similar to those of MORB and most Izu‐Bonin‐Mariana (IBM) back‐arc lavas. However, Ti/V and Yb/V ratios are lower in FAB reflecting a stronger prior depletion of their mantle source compared to the source of basalts from mid‐ocean ridges and back‐arc basins. Some FAB also have higher concentrations of fluid‐soluble elements than do spreading center lavas. Thus, the most likely origin of FAB is that they were the first lavas to erupt when the Pacific Plate began sinking beneath the Philippine Plate at about 51 Ma. The magmas were generated by mantle decompression during near‐trench spreading with little or no mass transfer from the subducting plate. Boninites were generated later when the residual, highly depleted mantle melted at shallow levels after fluxing by a water‐rich fluid derived from the sinking Pacific Plate. This magmatic stratigraphy of FAB overlain by transitional lavas and boninites is similar to that found in many ophiolites, suggesting that ophiolitic assemblages might commonly originate from near‐trench volcanism caused by subduction initiation. Indeed, the widely dispersed Jurassic and Cretaceous Tethyan ophiolites could represent two such significant subduction initiation events.

The transport and degassing pathways of volatiles through large silicic magmatic systems are central to understanding geothermal fluid compositions, ore deposit genesis, and volcanic eruption dynamics and impacts. Here, we document sulfur (S), chlorine (Cl), and fluorine (F) concentrations in a range of host materials in eruptive deposits from Taupō volcano (New Zealand). Materials analysed are groundmass glass, silicic melt inclusions, and microphenocrystic apatite that equilibrated in shallow melt-dominant magma bodies; silicic melt and apatite inclusions within crystal cores inferred to be sourced from deeper crystal mush; and olivine-hosted basaltic melt inclusions from mafic enclaves that represent the most primitive feedstock magmas. Sulfur and halogen concentrations each follow distinct concentration pathways during magma differentiation in response to changing pressures, temperatures, oxygen fugacities, crystallising mineral phases, the effects of volatile saturation, and the presence of an aqueous fluid phase. Sulfur contents in the basaltic melt inclusions (~ 2000 ppm) are typical for arc-type magmas, but drop to near detection limits by dacitic compositions, reflecting pyrrhotite crystallisation at ~ 60 wt. % SiO 2 during the onset of magnetite crystallisation. In contrast, Cl increases from ~ 500 ppm in basalts to ~ 2500 ppm in dacitic compositions, due to incompatibility in the crystallising phases. Fluorine contents are similar between mafic and silicic compositions (< 1200 ppm) and are primarily controlled by the onset of apatite and/or amphibole crystallisation and then destabilisation. Sulfur and Cl partition strongly into an aqueous fluid and/or vapour phase in the shallow silicic system. Sulfur contents in the rhyolite melts are low, yet the Oruanui supereruption is associated with a major sulfate peak in ice core records in Antarctica and Greenland, implying that excess S was derived from a pre-eruptive gas phase, mafic magma recharge, and/or disintegration of a hydrothermal system. We estimate that the 25.5 ka Oruanui eruption ejected > 130 Tg of S (390 Tg sulfate) and up to ~ 1800 Tg of Cl, with potentially global impacts on climate and stratospheric ozone.

Lava domes pose a significant hazard to infrastructure, human lives and the environment when they collapse. Their stability is partly dictated by internal mechanical properties. Here, we present a detailed investigation into the lithology and composition of a < 250-year-old lava dome exposed at the summit of Mt. Taranaki in the western North Island of New Zealand. We also examined samples from 400 to 600-year-old block-and-ash flow deposits, formed by the collapse of earlier, short-lived domes extruded at the same vent. Rocks with variable porosity and groundmass crystallinity were compared using measured compressive and tensile strength, derived from deformation experiments performed at room temperature and low (3 MPa) confining pressures. Based on data obtained, porosity exerts the main control on rock strength and mode of failure. High porosity (> 23%) rocks show low rock strength (< 41 MPa) and dominantly ductile failure, whereas lower porosity rocks (5–23%) exhibit higher measured rock strengths (up to 278 MPa) and brittle failure. Groundmass crystallinity, porosity and rock strength are intercorrelated. High groundmass crystal content is inversely related to low porosity, implying crystallisation and degassing of a slowly undercooled magma that experienced rheological stiffening under high pressures deeper within the conduit. This is linked to a slow magma ascent rate and results in a lava dome with higher rock strength. Samples with low groundmass crystallinity are associated with higher porosity and lower rock strength, and represent magma that ascended more rapidly, with faster undercooling, and solidification in the upper conduit at low pressures. Our experimental results show that the inherent strength of rocks within a growing dome may vary considerably depending on ascent/emplacement rates, thus significantly affecting dome stability and collapse hazards.

We present major, trace element, and Pb‐Sr‐Nd‐Hf isotope data for Quaternary basalt and basaltic andesite lavas from cross‐chain volcanoes in the northern Izu (N‐Izu) arc. Lavas from Izu‐Oshima, Toshima, Udonejima, and Niijima islands show consistent chemical changes with depth to the Wadati‐Benioff zone, from 120 km beneath Izu‐Oshima to 180 km beneath Niijima. Lavas from Izu‐Oshima at the volcanic front (VF) have elevated concentrations of large ion lithophile elements (LILEs), whereas rear‐arc (RA) lavas are rich in light rare earth elements (LREEs) and high field strength elements (HFSEs). VF lavas also have more radiogenic Pb, Nd, Sr, and Hf isotopic compositions. We have used the Arc Basalt Simulator version 3 (ABS3) to examine the mass balance of slab dehydration and melting and slab fluid/melt‐fluxed mantle melting and to quantitatively evaluate magma genesis beneath N‐Izu. The results suggest that the slab‐derived fluids/melts are derived from ∼20% sediment and ∼80% altered oceanic crust, the slab fluid is generated by slab dehydration for the VF magmas at 3.3–3.5 GPa/660°C–700°C, and slab melt for RA magmas is supplied at 3.4–4.4 GPa/830°C–890°C. The degree of fluxed melting of the mantle wedge varies between 17% and 28% (VF) and 6% and 22% (RA), with a slab flux fraction of 2%–4.5% (VF fluid) to 1%–1.5% (RA melt), and at melting depths 1–2.5 GPa (VF) and 2.4–2.8 GPa (RA). These conditions are consistent with a model whereby shallow, relatively low temperature slab fluids contribute to VF basalt genesis, whereas deeper and hotter slab melts control formation of RA basalts. The low‐temperature slab dehydration is the cause of elevated Ba/Th in VF basalt due mainly to breakdown of lawsonite, whereas deeper breakdown of phengite by slab melting is the cause of elevated K and Rb in RA basalts. Melting in the garnet stability field, and at lower degrees of partial melting, is required for the elevated LILEs, LREEs, and HFSEs observed in the RA basalts. Less radiogenic Sr, Nd, Hf, and Pb in RA basalts are all attributable to lesser slab flux additions. The low H2O predicted for RA basalt magmas (<1.5 wt %) relative to that in VF basalt magmas (5–8 wt %) is also due to melt addition rather than fluid. All these conclusions are broadly consistent with existing models; however, in this study they are quantitatively confirmed by the geochemical mass balance deduced from petrological ABS3 model. Overall, the P‐T‐X(H2O) structure of the slab and the mantle wedge exert the primary controls on arc basalt genesis.

We examine the connected history of dacite-dominant volcanic rocks of the Tschicoma Formation, erupted between 5.5 and 2 Ma from the Jemez Mountains volcanic field, western USA. Zircon samples from two separate eruptions have continuous SHRIMP U–Pb age spectra spanning 0.84–1.08 Myr duration (3.12–3.96 Ma and 3.50–4.58 Ma, respectively), following an episode of zircon crystallization 0.28–0.50 Myr earlier (at 4.46 Ma and 4.86 Ma, respectively). Zircon chemical variations, as well as ubiquitous resorption textures that commonly show large core-rim age differences (up to 720–740 kyr), suggest that they grew in separate melt lenses. Zircons were likely stored at near-solidus or even sub-solidus conditions after crystallization, but may have been reactivated in response to at least four major magma recharge events every 300–400 kyr and smaller events in between. A cycle of zircon dissolution (from heating), recrystallization (during cooling), and storage repeated in different locations in the Tschicoma mush system throughout its lifespan; each recharge-induced heating stage may last for several hundred to more than a thousand years based on calculations of zircon dissolution. We envisage the melt lenses to be distributed in a crystal mush zone, coalescing into a single magma batch as magma recharge occurs shortly before eruption. Once active, increasing magma supply rates may trigger large-scale partial melting of the pre-existing mush and caldera-forming eruptions.

Volcanic gas emissions and fluxes are crucial inputs to hazard assessments and global volatile budgets. However, for many volcanic areas (such as the Auckland Volcanic Field [AVF], a distributed basaltic system that underlies New Zealand’s largest population centre) neither directly measured nor analogue gas emissions data are readily available. In lieu of measured gas emissions data, we apply the petrologic method, using data from crystal-hosted melt inclusions and volcanic glass to calculate volatile emissions for a compositionally representative set of five AVF eruptions. Our results indicate that emissions from small-volume eruptions can rival those from polygenetic eruptions. Extrapolating this data for all 53 eruptive centres suggests that the AVF has emitted ~26,000 kt CO 2 , ~9,000 kt ~SO 2 , ~470 kt HCl, and ~2220 kt HF over its ~200 ky eruptive history. We extend our analysis to develop an estimate of volatile emissions during open- and closed-system degassing and model daily fluxes for eight previously developed AVF eruption scenarios. Scenario unrest timelines were coupled with a thermodynamic magma degassing model, EVo , to estimate open-system fluxes. For closed-system fluxes, we distributed scenario emissions over a simple log-normal magma discharge curve defined by the scenario eruption durations and data from the literature. We find that maximum, time-averaged daily SO 2 fluxes from distributed eruptions can be as high as those that have posed significant volcanic gas hazards to nearby populations, such as at La Palma in 2021. However, this is heavily dependent on scenario model inputs. Our results and the methodology may be used to estimate volcanic gas emissions and fluxes in other long dormant or unmonitored volcanic areas.

The transport and degassing pathways of volatiles through large silicic magmatic systems are central to understanding geothermal fluid compositions, ore deposit genesis, and volcanic eruption dynamics and impacts. Here, we document sulfur (S), chlorine (Cl), and fluorine (F) concentrations in a range of host materials in eruptive deposits from TaupÅ volcano (New Zealand). Materials analysed are groundmass glass, silicic melt inclusions, and microphenocrystic apatite that equilibrated in shallow melt-dominant magma bodies; silicic melt and apatite inclusions within crystal cores inferred to be sourced from deeper crystal mush; and olivine-hosted basaltic melt inclusions from mafic enclaves that represent the most primitive feedstock magmas. Sulfur and halogen concentrations each follow distinct concentration pathways during magma differentiation in response to changing pressures, temperatures, oxygen fugacities, crystallising mineral phases, the effects of volatile saturation, and the presence of an aqueous fluid phase. Sulfur contents in the basaltic melt inclusions ( 2000 ppm) are typical for arc-type magmas, but drop to near detection limits by dacitic compositions, reflecting pyrrhotite crystallisation at 60 wt. % SiO.sub.2 during the onset of magnetite crystallisation. In contrast, Cl increases from 500 ppm in basalts to 2500 ppm in dacitic compositions, due to incompatibility in the crystallising phases. Fluorine contents are similar between mafic and silicic compositions ( 130 Tg of S (390 Tg sulfate) and up to 1800 Tg of Cl, with potentially global impacts on climate and stratospheric ozone.

The halogen-bearing minerals tourmaline, amphibole, and biotite formed during magmatic–hydrothermal processes associated with the late-stage cooling of the Spirit Lake granitoid pluton (Mt. St. Helens, WA) and with the younger sulphide-mineralised rocks of the Margaret Cu–Mo porphyry deposit located entirely within the pluton. Major- and trace-element discrimination suggests that one tourmaline population crystallised from fractionated late-stage melt pockets in granodiorite–monzogranitic dykes of the pluton. These coarse, euhedral, oscillatory, and complexly sector-zoned uvite tourmalines span a limited range in Mg/(Mg + Fe) [Mg#] space (0.4–0.7 apfu) and show the highest Ti, Ca, F, Nb, and Ta contents, and low X-site vacancies (<0.1 apfu), suggesting slow, ordered crystallisation. Conversely, smaller, microcrystalline, pluton-related vein tourmalines show higher X-site vacancies (>0.6 apfu), lower Ca and F contents, and the highest Li, As, and HREE contents (>80 ppm Li, >1200 ppm As). This population appears to record direct, rapid crystallisation from magmatic ± meteoric fluid(s) bearing the signature of the breakdown of primary feldspars and pyroxenes, with fluid exsolution from fractionated melt patches likely triggered by the formation of the previous generation of tourmaline. Mineralised porphyry deposit tourmaline compositions from the stockwork span a much larger range in Mg# space (0.05–0.9 apfu) and are almost entirely Ca-free. X-sites of these schorl tourmalines are dominated by Na or vacancies, and the Y-sites are strongly Fe enriched. The highest Mn and Zn concentrations (>4000 and >1000 ppm, respectively) potentially reflect the composition of mineralising fluids during ore deposition. A number of boron isotopic analyses yield predominantly heavy boron, but δ 11 B values range from −5.2 to 6.2 ‰ and average 1.4 ‰. Whilst most plutonic tourmalines conform to reported a - and c -sector element partitioning models, those from the mineralised porphyry show large and variable sector fractionation differences, suggesting that external controls may also be important. Wider evidence for late-stage pervasive metasomatism by halogen-bearing exsolved fluid(s) is provided by the high Mg# (>70) secondary amphiboles and biotites from within the Spirit Lake pluton, where the amphiboles are clear replacement products of primary pyroxenes. Fluid halogen fugacity ratios calculated from the biotite compositions overlap with other global mineralised porphyry systems, despite not being immediately associated with sulphide ores. The evidence suggests complex fluid processes and the coincidental development of the mineralised porphyry system within the pluton. Heat, fluids, and metals were therefore likely supplied by a later phase of magmatism, unrelated to the consolidation of the main Spirit Lake granitoid. These new constraints on magmatic–hydrothermal fluid signatures have wider applicability to potentially tracing proximal barren and mineralised processes, and for distinguishing between formation mechanisms for primary and secondary halogen-bearing minerals.

Small eruptive centres (SECs) representing short-lived, isolated eruptions are effective samples of mantle heterogeneity over a given area, as they are generally of basaltic composition and show evidence of little magmatic processing. This is particularly powerful in volcanic arcs where the original melting process generating stratovolcanoes is often obscured by additions from the down-going slab (fluids and sediments) and the overlying crust. The Pucón area of southern Chile contains active and dormant stratovolcanoes, Holocene, basaltic SECs and an arc-scale strike-slip fault (the Liquiñe Ofqui Fault System: LOFS). The SECs show unexpected compositional heterogeneity considering their spatial proximity. We present a detailed study of these SECs combining whole rock major and trace element concentrations, U-Th isotopes and olivine-hosted melt inclusion major element and volatile contents to highlight the complex inter-relations in this small but active area. We show that heterogeneity preserved at individual SECs relates to different processes: some start in the melting region with the input of slab-derived fluids, whilst others occur later in a centre’s magmatic history with the influence of crustal contamination prior to olivine crystallisation. These signals are deduced through the combination of the different geochemical tools used in this study. We show that there is no correlation between composition and distance from the arc front, whilst the local tectonic regime has an effect on melt composition: SECs aligned along the LOFS have either equilibrium U-Th ratios or small Th-excesses instead of the large—fluid influenced—U-excesses displayed by SECs situated away from this feature. One of the SECs is modelled as being generated from fluid-enriched depleted mantle, a source which it may share with the stratovolcano Villarrica, whilst another SEC with abundant evidence of crustal contamination may share its plumbing system with its neighbouring stratovolcano Quetrupillán, showing that polygenetic–monogenetic connections are unpredictable. Such marked preservation of individual magmatic histories highlights the isolation of individual melting events even in complex and highly volcanically active areas.

In July and August of 2006 and May of 2010, Tungurahua volcano, Ecuador, produced pyroclastic flow-forming eruptions, representing increased explosivity compared to the Strombolian events that characterized its behavior since its renewal in 1999. Volatiles (H 2 O, CO 2 , S, Cl) and major elements were analyzed in 35 melt inclusions hosted in olivine and pyroxene phenocrysts in tephra from both events to reconstruct the pre-eruptive magmatic conditions and mechanisms that led to these more explosive episodes. Melt inclusion composition paired with host phenocryst zonation indicate mixing of two distinct magmas: a volatile-rich (∼4.0 wt% H 2 O and ∼1,800 ppm S) basaltic andesite containing olivine phenocrysts and a degassed (∼1.0 wt% H 2 O and 100–500 ppm S) andesite with plagioclase and pyroxene phenocrysts that contain andesitic to dacitic melt inclusions. We attribute the lower volatile concentrations in the evolved melt inclusions to degassing that occurred during residence in a shallow reservoir, where fractional crystallization led to the production of dacitic melt. Our melt inclusion data confirm the hypothesis made on the basis of phenocryst zoning profiles (J Volcanol Geotherm Res 199:69–84, 2011) that the intrusion of a volatile-rich basaltic andesite into a more evolved chamber and subsequent mixing led to explosive eruption in 2006. Melt inclusions from the 2006 and 2010 eruptive products have comparable volatile and major element compositions. High H 2 O concentrations in melt inclusions from 2010 olivine indicate little diffusive loss from the melt inclusions following mixing with the degassed andesitic reservoir, which requires that the 2010 eruption be the result of a new recharge event and not remobilization of the 2006 hybrid.