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The 6-month-long 2014–2015 Holuhraun eruption was the largest in Iceland for 200 years, emitting huge quantities of sulfur dioxide (SO2) into the troposphere, at times overwhelming European anthropogenic emissions. Weather, terrain and latitude made continuous ground-based or UV satellite sensor measurements challenging. Infrared Atmospheric Sounding Interferometer (IASI) data are used to derive the first time series of daily SO2 mass present in the atmosphere and its vertical distribution over the entire eruption period. A new optimal estimation scheme is used to calculate daily SO2 fluxes and average e-folding time every 12 h. For the 6 months studied, the SO2 flux was observed to be up to 200 kt day−1 and the minimum total SO2 erupted mass was 4.4±0.8 Tg. The average SO2 e-folding time was 2.4±0.6 days. Where comparisons are possible, these results broadly agree with ground-based near-source measurements, independent remote-sensing data and values obtained from model simulations from a previous paper. The results highlight the importance of using high-resolution time series data to accurately estimate volcanic SO2 emissions. The SO2 mass missed due to thermal contrast is estimated to be of the order of 3 % of the total emission when compared to measurements by the Ozone Monitoring Instrument. A statistical correction for cloud based on the AVHRR cloud-CCI data set suggested that the SO2 mass missed due to cloud cover could be significant, up to a factor of 2 for the plume within the first kilometre from the vent. Applying this correction results in a total erupted mass of 6.7±0.4 Tg and little change in average e-folding time. The data set derived can be used for comparisons to other ground- and satellite-based measurements and to petrological estimates of the SO2 flux. It could also be used to initialise climate model simulations, helping to better quantify the environmental and climatic impacts of future Icelandic fissure eruptions and simulations of past large-scale flood lava eruptions.

The Late Triassic Carnian Pluvial Episode (CPE) was a time of biological turnover and environmental perturbations. Within the CPE interval, C-isotope and sedimentary records indicate multiple pulses of depleted carbon into the atmosphere–ocean system linked to discrete enhancements of the hydrological cycle. Data suggest a similar cascade of events to other extinctions, including being potentially driven by emplacement of a large igneous province (LIP). The age of the Wrangellia LIP overlaps that of the CPE, but a direct link between volcanism and the pulsed CPE remains elusive. We present sedimentary Hg concentrations from Western Tethys successions to investigate volcanic activity through the previously established CPE global negative C-isotope excursions (NCIEs). Higher Hg concentrations and Hg/TOC are recorded just before and during NCIEs and siliciclastic inputs. The depositional settings suggest volcanic Hg inputs into the basins over the NCIEs rather than increases of Hg drawdown or riverine transport. Differences in Hg and Hg/TOC signals between the basins might be linked to coeval LIP style or the temporal resolution of the sedimentary successions. Overall, our new data provide support for a link between pulses of Wrangellia LIP volcanism, NCIEs, and humid phases that mark the CPE in the Western Tethys.

Long-lived basaltic volcanic eruptions are a globally important source of environmentally reactive, volatile metal pollutant elements such as selenium, cadmium and lead. The 2018 eruption of Kīlauea, Hawai’i produced exceptionally high discharge of metal pollutants, and was an unprecedented opportunity to track them from vent to deposition. Here we show, through geochemical sampling of the plume that volatile metal pollutants were depleted in the plume up to 100 times faster than refractory species, such as magnesium and iron. We propose that this rapid wet deposition of complexes containing reactive and potentially toxic volatile metal pollutants may disproportionately impact localised areas close to the vent. We infer that the relationship between volatility and solubility is an important control on the atmospheric behaviour of elements. We suggest that assessment of hazards from volcanic emissions should account for heterogeneous plume depletion of metal pollutants. Volatile metal pollutants in basaltic volcanic plumes can be deposited up to 100 times faster than refractory species, and may produce disproportionate impacts at proximal locations, according to extensive sampling of Kīlauea’s 2018 eruption plume.

Explosive, caldera-forming eruptions are exceptional and hazardous volcanic phenomena. The 1883 eruption of Krakatau is the largest such event for which there are detailed contemporary written accounts, allowing information on the eruptive progression to be integrated with the stratigraphy and geochemistry of its products. Freshly exposed sequences of the 1883 eruptive deposits of Krakatau, stripped of vegetation by a tsunami generated by the flank collapse of Anak Krakatau in 2018, shed new light on the eruptive sequence. Matrix glass from the base of the stratigraphy is chemically distinct and more evolved than the overlying sequence indicating the presence of a shallow, silicic, melt-rich region that was evacuated during the early eruptive activity from May 1883 onwards. Disruption of the shallow, silicic magma may have led to the coalescence and mixing of chemically similar melts representative of a range of magmatic conditions, as evidenced by complex and varied plagioclase phenocryst zoning profiles. This mixing, over a period of two to three months, culminated in the onset of the climactic phase of the eruption on 26th August 1883. Pyroclastic density currents (PDCs) emplaced during this phase of the eruption show a change in transport direction from north east to south west, coinciding with the deposition of a lithic lag breccia unit. This may be attributed to partial collapse of an elevated portion of the island, resulting in the removal of a topographic barrier. Edifice destruction potentially further reduced the overburden on the underlying magmatic system, leading to the most explosive and energetic phase of the eruption in the morning of 27th August 1883. This phase of the eruption culminated in a final period of caldera collapse, which is recorded in the stratigraphy as a second lithic lag breccia. The massive PDC deposits emplaced during this final phase contain glassy blocks up to 8 m in size, observed for the first time in 2019, which are chemically similar to the pyroclastic sequence. These blocks are interpreted as representing stagnant, shallow portions of the magma reservoir disrupted during the final stages of caldera formation. This study provides new evidence for the role that precursory eruptions and amalgamation of shallow crustal magma bodies potentially play in the months leading up to caldera-forming eruptions.

Funder: EPSRC-CASE studentship, Funder: NERC studentship, Funder: Leverhulme Trust; doi: https://doi.org/10.13039/501100000275, Funder: NERC-CASE studentship, Funder: Rolex Institute, Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava–seawater interaction (laze) plumes from the 2018 eruption of Kīlauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S2− ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.

The Paleocene–Eocene Thermal Maximum (PETM) was a period of geologically-rapid carbon release and global warming ~56 million years ago. Although modelling, outcrop and proxy records suggest volcanic carbon release occurred, it has not yet been possible to identify the PETM trigger, or if multiple reservoirs of carbon were involved. Here we report elevated levels of mercury relative to organic carbon—a proxy for volcanism—directly preceding and within the early PETM from two North Sea sedimentary cores, signifying pulsed volcanism from the North Atlantic Igneous Province likely provided the trigger and subsequently sustained elevated CO2. However, the PETM onset coincides with a mercury low, suggesting at least one other carbon reservoir released significant greenhouse gases in response to initial warming. Our results support the existence of ‘tipping points’ in the Earth system, which can trigger release of additional carbon reservoirs and drive Earth’s climate into a hotter state., The Paleocene–Eocene boundary coincided with runaway global warming possibly analogous to future climate change, but the sources of greenhouse gasses have remained unresolved. Here, the authors reveal volcanism triggered initial warming, and subsequent carbon was released after crossing a tipping point.

International audience; Among the hazards posed by volcanoes are the emissions of gases and particles that can affect air quality and damage agriculture and infrastructure. A recent intense episode of volcanic degassing associated with severe impacts on air quality accompanied the 2018 lower East Rift Zone (LERZ) eruption of Kīlauea volcano, Hawai'i. This resulted in a major increase in gas emission rates with respect to usual emission values for this volcano, along with a shift in the source of the dominant plume to a populated area on the lower flank of the volcano. This led to reduced air quality in downwind communities. We analyse open-access data from the permanent air quality monitoring networks operated by the Hawai'i Department of Health (HDOH) and National Park Service (NPS), and report on measurements of atmospheric sulfur dioxide (SO 2) between 2007 and 2018 and PM 2.5 (aerosol particulate matter with diameter

Mercury (Hg) is increasingly being used as a sedimentary tracer of Large Igneous Province (LIP) volcanism, and supports hypotheses of a coincidence between the formation of several LIPs and episodes of mass extinction and major environmental perturbation. However, numerous important questions remain to be answered before Hg can be claimed as an unequivocal fingerprint of LIP volcanism, as well as an understanding of why some sedimentary records document clear Hg enrichment signals whilst others do not. Of particular importance is evaluating the impact of different volcanic styles on the global mercury cycle, as well as the role played by depositional processes in recording global Hg-cycle perturbations. Here, new mercury records of Cretaceous Oceanic Anoxic Event 2 (OAE 2: ∼94 Ma) and the latest Cretaceous (∼67–66.0 Ma) are presented. OAE 2 is associated with the emplacement of multiple, predominantly submarine, LIPs; the latest Cretaceous with subaerial volcanism of the Deccan Traps. Both of these connections are strongly supported by previously published trends towards unradiogenic osmium- (Os) isotope values in globally distributed sedimentary records. Hg data from both events show considerable variation between different locations, attributed to the effectiveness of different sediment types in registering the Hg signal, with lithologically homogeneous records documenting more clear Hg enrichments than sections with major changes in lithology such as limestones to claystones or organic-rich shales. Crucially, there is no geographically consistent signal of sedimentary Hg enrichment in stratigraphic records of either OAE 2 or the latest Cretaceous that matches Os-isotope evidence for LIP emplacement, indicating that volcanism did not cause a global Hg perturbation throughout the entire eruptive history of the LIPs formed at those times. It is suggested that the discrepancy between Os-isotope and Hg trends in records of OAE 2 is caused by the limited dispersal range of Hg emitted from submarine volcanoes compared to the global-scale distribution of Os. A similar lack of correlation between these two proxies in uppermost Cretaceous strata indicates that, although subaerial volcanism can perturb the global Hg cycle, not all subaerial eruptions will do so. These results highlight the variable impact of different volcanogenic processes on the efficiency of Hg dispersal across the globe. Factors that could influence the impact of LIP eruptions on the global mercury cycle include submarine versus subaerial volcanism, volcanic intensity or explosivity, and the potential contribution of thermogenic mercury from reactions between ascending magma and surrounding organic-rich sediments.

Oceanic Anoxic Event 2 (OAE 2), during the Cenomanian–Turonian transition (∼94 Ma), was the largest perturbation of the global carbon cycle in the mid-Cretaceous and can be recognized by a positive carbon-isotope excursion in sedimentary strata. Although OAE 2 has been linked to large-scale volcanism, several large igneous provinces (LIPs) were active at this time (e.g. Caribbean, High Arctic, Madagascan, Ontong-Java) and little clear evidence links OAE 2 to a specific LIP. The Mid-Cenomanian Event (MCE, ∼96 Ma), identified by a small, 1 ‰ positive carbon-isotope excursion, is often referred to as a prelude to OAE 2. However, no underlying cause has yet been demonstrated and its relationship to OAE 2 is poorly constrained. Here, we report sedimentary mercury (Hg) concentration data from four sites, three from the southern margin of the Western Interior Seaway and one from Demerara Rise, in the equatorial proto-North Atlantic Ocean. We find that, in both areas, increases in mercury concentrations and Hg/TOC ratios coincide with the MCE and the OAE 2. However, the increases found in these sites are of a lower magnitude than those found in records of many other Mesozoic events, possibly characteristic of a marine rather than atmospheric dispersal of mercury for both events. Combined, the new mercury data presented here are consistent with an initial magmatic pulse at the time of the MCE, with a second, greater pulse at the onset of OAE 2, possibly related to the emplacement of LIPs in the Pacific Ocean and/or the High Arctic.

Deep carbon emissions from historically inactive volcanoes, hydrothermal, and tectonic structures are among the greatest unknowns in the long-term (∼Myr) carbon cycle. Recent estimates of diffuse CO2 flux from the Eastern Rift of the East African Rift System (EARS) suggest this could equal emissions from the entire mid-ocean ridge system. We report new CO2 surveys from the Main Ethiopian Rift (MER, northernmost EARS), and reassess the rift-related CO2 flux. Since degassing in the MER is concentrated in discrete areas of volcanic and off-edifice activity, characterization of such areas is important for extrapolation to a rift-scale budget. Locations of hot springs and fumaroles along the rift show numerous geothermal areas away from volcanic edifices. With these new data, we estimate total CO2 emissions from the central and northern MER as 0.52–4.36 Mt yr−1. Our extrapolated flux from the Eastern Rift is 3.9–32.7 Mt yr−1 CO2, overlapping with lower end of the range presented in recent estimates. By scaling, we suggest that 6–18 Mt yr−1 CO2 flux can be accounted for by magmatic extension, which implies an important role for volatile-enriched lithosphere, crustal assimilation, and/or additional magmatic intrusion to account for the upper range of flux estimates. Our results also have implications for the nature of volcanism in the MER. Many geothermal areas are found >10 km from the nearest volcanic center, suggesting ongoing hazards associated with regional volcanism.

International audience; Measuring the low bromine abundances in Earth’s materials remains an important challenge in order to constrain the geodynamical cycle of this element. Suitable standard materials are therefore required to establish reliable analytical methods to quantify Br abundances. In this study we characterise 21 Br-doped glasses synthesized from natural volcanic rocks of mafic to silicic compositions, in order to produce a new set of standards for Br analyses using various techniques. The nominal Br contents (amounts of Br loaded in the experimental samples) of 15 of 21 glasses were confirmed within 20% by instrumental neutron activation analysis (INAA). Using this new set of standards, we compare three micro-analytical approaches to measure Br contents in silicate glasses: synchrotron X-ray fluorescence (SR-XRF), laser ablation-inductively coupled plasma mass spectrometry (LA-ICP-MS), and secondary ion mass spectrometry (SIMS). With SR-XRF, the Br contents of the standard glasses were determined with the highest accuracy (< 10% for Br ≥ 10 ppm; > 25% for Br ≤ 5 ppm), and high precision (< 10% for Br contents > 10 ppm; 20-30% for Br ≤ 10 ppm). The detection limit was estimated to be less than 1 ppm Br. All those factors combined with a high spatial resolution (5x5 μm for the presented measurements), means that SR-XRF is well suited to determine the low Br abundance in natural volcanic glasses (crystal-hosted melt inclusions or matrix glasses of crystallized samples). At its current stage of development, the LA-ICP-MS method allows the measurement of hundreds to thousands ppm Br in silicate glasses with a precision and accuracy generally within 20 %. The Br detection limit of this method has not been estimated but its low spatial resolution (90 μm) currently prevents its use to characterise natural volcanic glasses, however it is fully appropriate to analyse super liquidus or sparsely phyric, Br-rich experimental charges. Our study shows that SIMS appears to be a promising technique to measure the low Br contents of natural volcanic glasses. Its spatial resolution is relatively good (~ 15 μm) and, similarly to SR-XRF, the detection limit is estimated to be ≤ 1 ppm. Using our new set of standards, the Br contents of two MPI-DING reference glasses containing less than 1.2 ppm of Br were reproduced with precision < 5% and accuracy < 20%. Moreover, SIMS presents the advantage of being a more accessible instrument than SR-XRF and data processing is more straightforward.

Distributed volcanic fields of scoria cones, maars, tuff cones and lava flows represent a crucial expression of the interplay between magmatism, tectonics and surface processes in continental rifts. We compare the cone morphology of two fields (Butajira and East Ziway) in the Main Ethiopian Rift (MER), using high-resolution digital elevation models (DEMs) to investigate volumes, surface environment and age of emplacement. Volumes of individual cones are similar in both fields (mean ~4 × 106 m3) and lower than in other distributed volcanic fields located in extensional environments. Volcanism at Butajira has created linear clusters of superimposed cones, suggesting a small number of larger (107–108 m3) fissure eruptions compared to the isolated events at East Ziway. The presence of maars and deep craters within cones at Butajira indicates phreatomagmatic activity, not seen at East Ziway where cones may have been emplaced during a dry climate phase. Shape parameters, including curvature of cone rims and ratios of cone height, width and crater depth, suggest younger eruption ages at Butajira compared to East Ziway and the possibility of ongoing activity in this area. A broader survey of cone fields across the MER using the ASTER global digital elevation model fails to identify systematic variation in height, width and volume from cone morphology, limited by low-resolution. High-resolution topography provides a useful insight into rift environments at the time of emplacement, and further surveys across the Main Ethiopian Rift may advance our understanding of distributed volcanism in extensional settings and the hazards they present.

Magmas from continental arcs built on thick crust have elevated incompatible element abundances and “enriched” radiogenic isotope ratios compared to magmas erupted in island and continental arcs overlying thinner crust. The relative influence of the slab, mantle, and upper plate on this variability is heavily debated. The Andean Southern Volcanic Zone (SVZ; 33–46°S) is an ideal setting to investigate the production of enriched continental arc compositions, because both crustal thickness and magma chemistry vary coherently along strike. However, the scarcity of primitive magmas in the thick-crusted northern SVZ has hindered previous regional studies. To better address the origin of enriched continental compositions, we investigate the geochemistry (major and trace element abundances, 87Sr/86Sr and 143Nd/144Nd ratios) of new mafic samples from Don Casimiro and Maipo volcanoes within the Diamante-Maipo Caldera Complex of the northern SVZ. While evolved Diamante-Maipo samples show evidence for crustal assimilation, the trace element and isotopic enrichment of the most mafic samples cannot result from crustal processing, as no known regional or global basement lithologies are enriched in all of the necessary incompatible trace elements. Subduction erosion models similarly fail to account for the enriched isotopic and trace element signature of these samples. Instead, we suggest that the enrichment of northern SVZ magmas is derived from an enriched ambient mantle component (similar to EM1-type ocean island basalts), superimposed on a northward decline in melt extent. A substantial, but nearly uniform contribution of melts from subducting sediment and altered oceanic crust are required at all latitudes. The EM1-like enrichment may arise from recycling of metasomatized subcontinental lithospheric mantle (M-SCLM), as the isotopic trajectory of primitive rear-arc monogenetic cones trend towards the compositions of SCLM melts sampled across South America. Isotopic data from spatially distributed rear-arc centres demonstrate that the arc-parallel variations in the degree of EM1-type enrichment observed in arc-front samples are also present up to 600 km behind the trench in the rear-arc. Rear-arc trace element systematics require significant but variable quantities of slab melts to be transported to the mantle wedge at these large trench distances. Overall, we show that a unified model incorporating variable mantle enrichment, slab additions, and melt extents can account for along and across-arc trends within the SVZ. The recognition that mantle enrichment plays a key role in the production of enriched continental compositions in the SVZ has important implications for our understanding of the chemical evolution of the Earth. If ambient mantle enrichment is not taken into account, petrogenetic models of evolved lavas may overestimate the role of crustal assimilation, which, in turn, may lead models of continental crust growth to overestimate the amount of continental material that has been recycled back into the mantle.

Santorini Volcano is an outstanding natural laboratory for studying arc volcanism, having had twelve Plinian eruptions over the last 350,000 years, at least four of which caused caldera collapse. Periods between Plinian eruptions are characterized by intra-caldera edifice construction and lower intensity explosive activity. The Plinian eruptions are fed from magma reservoirs at 4–8 km depth that are assembled over several centuries prior to eruption by the arrival of high-flux magma pulses from deeper in the sub-caldera reservoir. Unrest in 2011–2012 involved intrusion of two magma pulses at about 4 km depth, suggesting that the behaviour of the modern-day volcano is similar to the behaviour of the volcano prior to Plinian eruptions. Emerging understanding of Santorini's plumbing system will enable better risk mitigation at this highly hazardous volcano.

As our ability to detect volcanic unrest improves, we are increasingly confronted with the question of whether the unrest has a magmatic origin (magma on the move) or a non-magmatic origin from a change in the hydrothermal system (fluids that are not magma on the move) or tectonic processes. The cause of unrest has critical implications for the potential eruptive hazard (e.g. used in constructing Bayesian Event Trees), but is frequently the subject of debate, even at well-studied systems. Here, we propose a set of multi-disciplinary observations and numerical models that could be used to evaluate conceptual models about the cause of unrest. These include measurements of gas fluxes and compositions and the isotopic signature of some components (e.g. H 2 , He, C, SO 2 , H 2 O , CH 4 and CO 2 ), the spatial and temporal characteristics of ground deformation, thermal output, seismicity, changes in gravity, and whether there is topographic uplift or subsidence spanning hundreds to thousands of years. In several volcanic systems, both magmatic and non-magmatic unrest is occurring at the same time. While none of these observations or models is diagnostic on its own, we illustrate several examples where they have been used together to make a plausible conceptual model of one or more episodes of unrest and whether eruptions did or did not follow the unrest. This article is part of the Theo Murphy meeting issue ‘Magma reservoir architecture and dynamics’.

Ash clouds are a geographically far reaching hazard associated with volcanic eruptions. To minimise the risk that these pose to aircraft and to limit disruption to the aviation industry, it is important to closely monitor the emission and atmospheric dispersion of these plumes. The altitude of the plume is an important consideration and is an essential input into many models of ash cloud propagation. CO2 slicing is an established technique for obtaining the top height of meteorological clouds and previous studies have demonstrated that there is potential for this method to be used for volcanic ash. In this study, the CO2 slicing technique has been adapted for volcanic ash and applied to spectra obtained from the Infrared Atmospheric Sounding Interferometer (IASI). Simulated ash spectra are first used to select the most appropriate channels and then demonstrate that the technique has merit for determining the altitude of the ash. These results indicate a strong match between the true heights and CO2 slicing output with a root mean square error (RMSE) of less than 800 m. Following this, the technique was applied to spectra obtained with IASI during the Eyjafjallajökull and Grimsvötn eruptions in 2010 and 2011 respectively, both of which emitted ash clouds into the troposphere, and which have been extensively studied with satellite imagery. The CO2 slicing results were compared against those from an optimal estimation scheme, also developed for IASI, and a satellite borne LiDAR is used for validation. Overall, the CO2 slicing tool performs better than the optimal estimation scheme. The CO2 slicing heights returned a RMSE value of 2.2 km when compared against the LiDAR. This is lower than the RMSE for the optimal estimation scheme (2.8 km). The CO2 slicing technique is a relatively fast tool and the results suggest that this method could be used to get a first approximation of the ash cloud height, potentially for use for hazard mitigation, or as an input for other retrieval techniques or models of ash cloud propagation.

Structure-from-motion (SfM) photogrammetry techniques are now widely available to generate digital terrain models (DTMs) from optical imagery, providing an alternative to costlier options such as LiDAR or satellite surveys. SfM could be a useful tool in hazard studies because its minimal cost makes it accessible even in developing regions and its speed of use can provide updated data rapidly in hazard-prone regions. Our study is designed to assess whether crowd-sourced SfM data is comparable to an industry standard LiDAR dataset, demonstrating potential real-world use of SfM if employed for disaster risk reduction purposes. Three groups with variable SfM knowledge utilized 16 different camera models, including four camera phones, to collect 1001 total photos in one hour of data collection. Datasets collected by each group were processed using VisualSFM, and the point densities, accuracies and distributions of points in the resultant point clouds (DTM skeletons) were compared. Our results show that the point clouds are resilient to inconsistency in users’ SfM knowledge: crowd-sourced data collected by a moderately informed general public yields topography results comparable in data density and accuracy to those produced with data collected by highly-informed SfM users or experts using LiDAR. This means that in a real-world scenario involving participants with a diverse range of expertise, topography models could be produced from crowd-sourced data quite rapidly and to a very high standard. This could be beneficial to disaster risk reduction as a relatively quick, simple and low-cost method to attain rapidly updated knowledge of terrain attributes, useful for the prediction and mitigation of many natural hazards.

International audience; Large igneous province (LIP) volcanism has been proposed as a key trigger of several major climate and environmental perturbations during the Phanerozoic Aeon. Large-scale carbon emissions associated with one or both of magmatic degassing from the Greater Ontong-Java Plateau (G-OJP) and intrusion of organic-rich sediments by High Arctic LIP (HALIP) sills have been widely suggested as the trigger of the Early Aptian Oceanic Anoxic Event (OAE 1a: ~120 Ma). However, the respective roles of the two LIPs and associated carbon sources in causing this crisis remain debated. Here, six records of OAE 1a from the Pacific, Tethyan, Arctic, and South Atlantic realms are investigated, combining mercury (Hg) concentrations and osmium- (Os-) isotope ratios as proxies of LIP activity. Together with previously published datasets, the results indicate globally consistent Os-isotope evidence for LIP activity during OAE 1a, but geographically variable stratigraphic Hg trends. Clear mercury enrichments that match Os-isotope evidence of LIP activity, and suggest a Hg-cycle perturbation during the onset of OAE 1a, are documented at one Pacific site extremely proximal to the G-OJP, but not in Arctic, Tethyan or Atlantic records. This pattern highlights significant G-OJP volcanism during the onset of OAE 1a, and re-emphasises the limited potential for submarine LIP eruptions to cause Hg-cycle perturbations except in areas very proximal to source. The absence of clear Hg peaks in basal OAE 1a strata from the Arctic (or anywhere outside of the Pacific) does not support intense HALIP activity at that time, suggesting that the G-OJP was the more volcanically active LIP when OAE 1a commenced. Thus, G-OJP emissions of mantle carbon were more likely to have played a major role in initiating OAE 1a than thermogenic volatiles associated with the HALIP. A transient pulse of HALIP-related subaerial eruptions and/or thermogenic volatile emissions during the early–middle part of OAE 1a, potentially evidenced by more widespread Hg enrichments in strata from that time (including in the Arctic), might have prolonged the event. However, a non-volcanic cause of these later Hg influxes cannot be excluded. These findings challenge previous suggestions that magmatic CO2 emissions from LIPs were incapable of causing major carbon-cycle perturbations alone, and highlight the need for further investigations to establish whether the high volume/emplacement rate of the G-OJP (potentially an order of magnitude greater than other LIPs) made it a unique case that stands in contrast to other provinces where the role of thermogenic volatiles was likely more crucial.

Understanding the climate history of Mars, one of our closest planetary neighbours, has important implications for understanding the environmental evolution of Earth and other rocky planets in general. The widespread recognition of an extensive sedimentary record modified, at least in part, by liquid water, holds much promise to provide evidence about Mars’ past. However, unravelling the pressure and compositional history of Mars’ Noachian atmosphere has remained problematic. Based on expected outgassing behaviour, observed atmospheric isotope ratios, and climate models, carbon dioxide is widely considered a main constituent of the early Martian atmosphere. If this was indeed the case, it is surprising that carbonate minerals, the expected sinks for this carbon, are only abundant in a few isolated localities across the Martian surface. Three broad possibilities may account for this apparent inconsistency: (1) carbonates formed under pCO2 higher than present but were buried, or subsequently destroyed; (2) Noachian atmospheric pCO2 was significantly lower than current estimates; or (3) low temperature carbonate formation was kinetically controlled under the aqueous conditions that characterised much of the early Martian surface. While orbital spectroscopic investigations have yielded an increasing inventory of isolated carbonate-bearing deposits, their relative rarity at the near-surface has prompted suggestions that the Noachian atmosphere was commonly characterised by low pCO2. Without a more complete investigation of the carbonate-forming processes occurring within the ancient crust, no hypothesis can be tested robustly. Here, we examine the controls on Fe(II)-carbonate precipitation in low-temperature, anoxic water-rock systems as a function of pCO2. In experiments lasting up to 85 days, no measurable Fe(II)- carbonate precipitation occurred within the limits of analytical detection, despite significant and sustained supersaturation with respect to siderite. These observations are quantitatively consistent with recent investigations highlighting a significant supersaturation threshold for Fe(II)-carbonate nucleation. Reaction path models that incorporate these constraints indicate that Fe(II)-carbonate supersaturation thresholds would have been commonly met in low water:rock ratio systems isolated from the Noachian atmosphere as opposed to high water:rock ratio, open systems exposed at the near surface. These results suggest the rarity of carbonates exposed at or near the surface of Mars may be controlled, at least in part, by a lack of deep crustal exposures and lack of the geochemical conditions conducive to carbonate formation, rather than insufficient atmospheric pCO2. Such geochemical constraints are in turn consistent with available orbital geological data indicating that carbonates may be more abundant within the deep crust, potentially representing a significant subsurface carbon sink.

Restless silicic calderas present major geological hazards, and yet many also host significant untapped geothermal resources. In East Africa, this poses a major challenge, although the calderas are largely unmonitored their geothermal resources could provide substantial economic benefits to the region. Understanding what causes unrest at these volcanoes is vital for weighing up the opportunities against the potential risks. Here we bring together new field and remote sensing observations to evaluate causes of ground deformation at Aluto, a restless silicic volcano located in the Main Ethiopian Rift (MER). Interferometric Synthetic Aperture Radar (InSAR) data reveal the temporal and spatial characteristics of a ground deformation episode that took place between 2008 and 2010. Deformation time series reveal pulses of accelerating uplift that transition to gradual long-term subsidence, and analytical models support inflation source depths of ∼5 km. Gases escaping along the major fault zone of Aluto show high CO2 flux, and a clear magmatic carbon signature (CO2-δ13C of −4.2‰ to −4.5‰). This provides compelling evidence that the magmatic and hydrothermal reservoirs of the complex are physically connected. We suggest that a coupled magmatic-hydrothermal system can explain the uplift-subsidence signals. We hypothesize that magmatic fluid injection and/or intrusion in the cap of the magmatic reservoir drives edifice-wide inflation while subsequent deflation is related to magmatic degassing and depressurization of the hydrothermal system. These new constraints on the plumbing of Aluto yield important insights into the behavior of rift volcanic systems and will be crucial for interpreting future patterns of unrest.

Sulfur dioxide (SO2) is an important atmospheric constituent that plays a crucial role in many atmospheric processes. Volcanic eruptions are a significant source of atmospheric SO2 and its effects and lifetime depend on the SO2 injection altitude. The Infrared Atmospheric Sounding Interferometer (IASI) on the METOP satellite can be used to study volcanic emission of SO2 using high-spectral resolution measurements from 1000 to 1200 and from 1300 to 1410 cm−1 (the 7.3 and 8.7 µm SO2 bands) returning both SO2 amount and altitude data. The scheme described in Carboni et al. (2012) has been applied to measure volcanic SO2 amount and altitude for 14 explosive eruptions from 2008 to 2012. The work includes a comparison with the following independent measurements: (i) the SO2 column amounts from the 2010 Eyjafjallajökull plumes have been compared with Brewer ground measurements over Europe; (ii) the SO2 plumes heights, for the 2010 Eyjafjallajökull and 2011 Grimsvötn eruptions, have been compared with CALIPSO backscatter profiles. The results of the comparisons show that IASI SO2 measurements are not affected by underlying cloud and are consistent (within the retrieved errors) with the other measurements. The series of analysed eruptions (2008 to 2012) show that the biggest emitter of volcanic SO2 was Nabro, followed by Kasatochi and Grímsvötn. Our observations also show a tendency for volcanic SO2 to reach the level of the tropopause during many of the moderately explosive eruptions observed. For the eruptions observed, this tendency was independent of the maximum amount of SO2 (e.g. 0.2 Tg for Dalafilla compared with 1.6 Tg for Nabro) and of the volcanic explosive index (between 3 and 5).

The Triassic–Jurassic transition is characterized by the end-Triassic mass extinction approximately synchronous with the onset of emplacement of the Central Atlantic Magmatic Province (CAMP), and associated with a major negative carbon-isotope excursion (CIE) affecting the ocean–atmosphere system. Here, we present new data (total organic carbon, pyrolysis analysis, carbon-isotopes from bulk organic matter, elemental mercury, and other elemental contents) from a southern-hemisphere Triassic–Jurassic boundary succession in the Neuquen Basin, Argentina. The end-Triassic mass extinction there coincides with a relatively small (2–3‰) negative CIE in bulk organic matter, and we present a model that suggests that extreme aridity across the western Pangaean landmass may have resulted in rather limited terrestrial organic-matter flux to the sedimentary realm in eastern Panthalassic marine basins, hypothetically reducing the magnitude of the observed negative CIE in δ13CTOC. Increased deposition of sedimentary Hg (and Hg/TOC and Hg/Zr) in the marine Neuquen Basin began stratigraphically before the negative CIE associated with the end-Triassic mass extinction, and thus before the commencement, in North America and Africa, of CAMP-related basaltic volcanism, but possibly coinciding with the early emplacement of CAMP-associated intrusives (dykes and sills). This relative chronology suggests thermal alteration of intruded country rocks and/or intrusive magmatic degassing of Hg as potential major sources of elevated Hg fluxes to the atmosphere at this time. The Neuquen Basin experienced the development of dysoxic–anoxic marine conditions across the Triassic–Jurassic transition, enabling increased preservation of organic matter. Simple mass-balance calculations show that enhanced carbon burial rates can explain the inferred evolution of the global exogenic carbon cycle across this time-interval.

The timing and processes that govern the end of volcanic eruptions are not yet fully understood, and there currently exists no systematic definition for the end of a volcanic eruption. Currently, end of eruption is established either by generic criteria (typically 90 days after the end of visual signals of eruption) or criteria specific to a given volcano. We explore the application of supervised machine learning classification methods: Support Vector Machine, Logistic Regression, Random Forest and Gaussian Process Classifiers and define a decisiveness index D to evaluate the consistency of the classifications obtained by these models. We apply these methods to seismic time series from two volcanoes chosen because they display contrasting styles of eruption: Telica (Nicaragua) and Nevado del Ruiz (Colombia). We find that, for both volcanic systems, the end-date we obtain by classification of seismic data is 2–4 months later than end-dates defined by the last occurrence of visual eruption (such as ash emission). This finding is in agreement with previous, general definitions of eruption end and is consistent across models. Our classifications have a higher correspondence of eruptive activity with visual activity than with database records of eruption start and end. We analyze the relative importance of the different features of seismic activity used in our models (e.g. peak event amplitude, daily event counts) and find little consistency between the two volcanic systems in terms of the most important features which determine whether activity is eruptive or non-eruptive. These initial results look promising and our approach may offer a robust tool to help determine when an eruption has ended in the absence of visual confirmation.

This project is funded by the Natural Environment Research Council grant NE/L013932/1 (RiftVolc). Abstract For many magmatic systems, crystal compositions preserve a complex and protracted history which may be largely decoupled from their carrier melts. The crystal cargo may hold clues to the physical distribution of melt and crystals in a magma reservoir and how magmas are assembled prior to eruptions. Here we present a geochemical study of a suite of samples from three peralkaline volcanoes in the Main Ethiopian Rift. Whilst whole-rock data shows strong fractional crystallisation signatures, the trace element systematics of feldspars, and their relationship to their host glasses, reveals complexity. Alkali feldspars, particularly those erupted during caldera-forming episodes, have variable Ba concentrations, extending to high values that are not in equilibrium with the carrier liquids. Some of the feldspars are antecrysts, which we suggest are scavenged from a crystal-rich mush. The antecrysts crystallised from a Ba-enriched (more primitive) melt, before later entrainment into a Ba-depleted residual liquid. Crystal-melt segregation can occur on fast timescales in these magma reservoirs, owing to the low viscosity nature of peralkaline liquids. The separation of enough residual melt to feed a crystal-poor post-caldera rhyolitic eruption may take as little as months to tens of years (much shorter than typical repose periods of 300-400 years). Our observations are consistent with these magmatic systems spending significant portions of their life cycle dominated by crystalline mushes containing ephemeral, small (

As well as gases that regulate climate over geological time, volcanoes emit prodigious quantities of metals into the atmosphere, where they have key roles as catalysts, pollutants and nutrients. Here we compare measurements of arc basaltic volcano metal emissions with those from hotspot settings. As well as emitting higher fluxes of metals (similar to those building ore deposits), these arc emissions possess a distinct compositional fingerprint, particularly rich in tungsten, arsenic, thallium, antimony and lead when compared with those from hotspots. We propose that volcanic metal emissions are controlled by magmatic water content and redox: hydrous arc magmas that do not undergo sulfide saturation yield metal-rich, saline aqueous fluid; shallow degassing and resorption of late-stage sulfides feeds volcanic gases in Hawai’i and Iceland. Although global arc magma chemistries vary considerably, our findings suggest that volcanic emissions in arcs have a distinct fingerprint when compared with other settings. A shift in global volcanic metal emissions may have occurred in Earth’s past as more oxidized, water-rich magmas became prevalent, influencing the surface environment. Arc volcanism emits higher metal fluxes to Earth’s atmosphere than hotspot volcanism. The systems’ unique gas compositions are controlled by magmatic water content and redox state, as shown by a compilation of volcanic gas and aerosol metal data.

Satellite remote sensing is a valuable method for detecting and quantifying sulfur dioxide (SO2) emissions at volcanoes. The use of ultraviolet satellite instruments for monitoring purposes has been assessed in numerous studies, but there are advantages to using infrared measurements, including that they can operate at night and during high-latitude winters. This study focuses on the Infrared Atmospheric Sounding Interferometer (IASI). Retrievals developed for this instrument have been shown to be successful when applied to large eruptions, but little has been done to explore their potential for detecting and quantifying emissions from smaller and lower altitude emissions or for the assessment of ongoing activity. Here a “fast” linear retrieval has been applied across the globe to detect volcanic sources of SO2. The results are dominated by emissions from explosive eruptions, but signals are also evident from weak eruptions, passive degassing, and anthropogenic activity. Ecuador and Kamchatka were selected for further study with a more processing intensive iterative retrieval which can quantify the SO2 amount. At Tungurahua in Ecuador, good agreement was seen between IASI, the Ozone Monitoring Instrument (OMI) and ground-based flux data, demonstrating that the retrieval is capable of capturing relative changes in activity. Similarly, good agreement was found between IASI and OMI in Kamchatka. In this high-latitude region, OMI is unable to operate for 3 or 4 months in each year. It is therefore suggested that IASI could be used alongside other instruments for evaluating changes in volcanic activity.

This work was funded by the Natural Environment Research Council grant NE/L013932/1 (RiftVolc) and a Boise Fund grant from the Department of Zoology, University of Oxford. The Main Ethiopian Rift (MER, ~7–9°N) is the type example of a magma-assisted continental rift. The rift axis is populated with regularly spaced silicic caldera complexes and central stratovolcanoes, interspersed with large fields of small mafic scoria cones. The recent (latest Pleistocene to Holocene) history of volcanism in the MER is poorly known, and no eruptions have occurred in the living memory of the local population. Assessment of contemporary volcanic hazards and associated risk is primarily based on the study of the most recent eruptive products, typically those emplaced within the last 10–20 ky. We integrate new and published field observations and geochemical data on tephra deposits from the main Late Quaternary volcanic centres in the central MER to assess contemporary volcanic hazards. Most central volcanoes in the MER host large mid-Pleistocene calderas, with typical diameters of 5–15 km, and associated ignimbrites of trachyte and peralkaline rhyolite composition. In contrast, post-caldera activity at most centres comprises eruptions of peralkaline rhyolitic magmas as obsidian flows, domes and pumice cones. The frequency and magnitude of events varies between individual volcanoes. Some volcanoes have predominantly erupted obsidian lava flows in their most recent post-caldera stage (Fentale), whereas other have had up to 3 moderate-scale (VEI 3–4) explosive eruptions per millennium (Aluto). At some volcanoes we find evidence for multiple large explosive eruptions (Corbetti, Bora-Baricha, Boset-Bericha) which have deposited several centimeters to meters of pumice and ash in currently densely populated regions. This new overview has important implications when assessing the present-day volcanic hazard in this rapidly developing region. Postprint

International audience; Volcanogenic halogens, in particular bromine, potentially play an important role in the ozone depletion of the atmosphere. Understanding bromine behaviour in magmas is therefore crucial to properly evaluate the contribution of volcanic eruptions to atmospheric chemistry and their environmental impact. To date, bromine partitioning between silicate melts and the gas phase is very poorly constrained, with the only relevant experimental studies limited to investigation of synthetic melt with silicic compositions. In this study, fluid/melt partitioning experiments were performed using natural silicate glasses with mafic, intermediate and silicic compositions. For each composition, experiments were run with various Br contents in the initial fluid (H2O–NaBr), at T–P conditions representative of shallow magmatic reservoirs in volcanic arc contexts (100–200 MPa, 900–1200 °C). The resulting fluid/melt partition coefficients (DBrf/m) are: 5.0 ± 0.3 at 1200 °C–100 MPa for the basalt, 9.1 ± 0.6 at 1060 °C–200 MPa for the andesite and 20.2 ± 1.2 at 900 °C–200 MPa for the rhyodacite. Our experiments show that DBrf/m increases with increasing SiO2 content of the melt (as for chlorine) and suggest that it is also sensitive to melt temperature (increase of DBrf/m with decreasing temperature). We develop a simple model to predict the S–Cl–Br degassing behaviour in mafic systems, which accounts for the variability of S–Cl–Br compositions of volcanic gases from Etna and other mafic systems, and shows that coexisting magmatic gas and melt evolve from S-rich to Cl–Br enriched (relative to S) upon increasing degree of degassing. We also report first Br contents for melt inclusions from Etna, Stromboli, Merapi and Santorini eruptions and calculate the mass of bromine available in the magma reservoir prior to the eruptions under consideration. The discrepancy that we highlight between the mass of Br in the co-existing melt and fluid prior to the Merapi 2010 eruption (433 and 73 tons, respectively) and the lack of observed BrO (from space) hints at the need to investigate further Br speciation in ‘ash-rich’ volcanic plumes. Overall, our results suggest that the Br yield into the atmosphere of cold and silicic magmas will be much larger than that from hotter and more mafic magmas.

J. Biggs, I.M.Watson, W. Hutchison, T.A. Mather and D.M. Pyle are members of the NERC Centre for the Observation and Modelling of Earthquakes, Volcanoes and Tectonics (COMET). This work forms a contribution to the NERC Large Grant RiftVolc (NE/L01372X/1) awarded to J. Biggs. W. Hutchison was funded by NERC studentship NE/J500045/1. I.M. Watson is part of the NASA-ASTER science team and acknowledges NASA and JAXA for the provision of data. Fumaroles are the surface manifestation of hydrothermal circulation and can be influenced by magmatic, hydrothermal, hydrological and tectonic processes. This study investigates the temporal changes in fumarole temperatures and spatial extent on Aluto, a restless volcano in the Main Ethiopian Rift (MER), in order to better understand the controls on fluid circulation and the interaction between the magmatic and hydrothermal systems. Thermal infrared (TIR) satellite images, acquired by the Advanced Spaceborne Thermal Emission and Reflection radiometer (ASTER) over the period of 2004 to 2016, are used to generate time series of the fumarole temperatures and areas. The thermal anomalies identified in the ASTER images coincide with known fumaroles with temperatures > 80 °C and are located on or close to fault structures, which provide a pathway for the rising fluids. Most of the fumaroles, including those along the major zone of hydrothermal upwelling, the Artu Jawe Fault Zone, have pixel-integrated temperature variations of only ~ 2 ± 1.5 °C. The exception are the Bobesa fumaroles located on a hypothesised caldera ring fault which show pixel-integrated temperature changes of up to 9 °C consistent with a delayed response of the hydrothermal system to precipitation. We conclude that fumaroles along major faults are strongly coupled to the magmatic-hydrothermal system and are relatively stable with time, whereas those along shallower structures close to the rift flank are more strongly influenced by seasonal variations in groundwater flow. The use of remote sensing data to monitor the thermal activity of Aluto provides an important contribution towards understanding the behaviour of this actively deforming volcano. This method could be used at other volcanoes around the world for monitoring and geothermal exploration. Postprint

Sulfides are a major potential repository for magmatic metals and sulfur. In relatively reduced magmas, there may be a dynamic interplay between sulfide liquids and magma degassing as magmas ascend/erupt. Sulfide-bubble aggregates may segregate to shallow levels. Exsolved fluids may oxidize sulfides to produce SO 2 gas and metals, which can vent to the atmosphere with chalcophile metal ratios reflecting those in their parent sulfide liquids. Sulfide breakdown and/or sequestration timing and balance define the role of sulfides in both ore formation and the environmental impacts of volcanic eruptions, including during the evolution of large igneous provinces, which are key periods of heightened volcanism during Earth history.

An enigmatic chloride-rich iron (oxyhydr)oxide has been recently identified together with mercury anomalies in End-Cretaceous marine sediments coeval with the Deccan Traps eruptions. The mineral was observed in Bidart (France) and Gubbio (Italy), suggesting a widespread phenomenon. However, the exact nature and origin of this Cl-bearing mineral remained speculative. Here, we characterized the accurate composition and nanostructure of this chloride-rich phase by using micro-Raman spectroscopy, Transmission (TEM) and Scanning (SEM) Electron Microscopy on Focused Ion Beam foils. We also provide new evidence of its occurrence in Zumaia, a reference KPg section from Spain. Results confirm akaganéite (β-FeOOH) as the main phase, with chloride content of 3–5 atomic weight %. Akaganéite particles are constituted by the aggregation of nanorods of akaganéite. Internal structures contain empty spaces, suggesting formation in a low-density (atmospheric) environment. This new mineralogical evidence supports the hypothesis that the observed akaganéite was formed in the Deccan volcanic plume and was transported to the Atlantic and Tethysian realms through the stratosphere. Therefore, akaganéite provides a potential new sedimentary marker to identify the imprint of the Deccan eruptions in the stratigraphic record and is evidence of volcanic halogen degassing and its potential role for the Cretaceous-Tertiary mass extinction.

Volcanic eruptions have been hypothesized as an iron supply mechanism for phytoplankton blooms; however, little direct evidence of stimulatory responses has been obtained in the field. Here we present the results of twenty-one 1–2 day bottle enrichment experiments from cruises in the South Atlantic and Southern Ocean which conclusively demonstrated a photophysiological and biomass stimulation of phytoplankton communities following supply of basaltic or rhyolitic volcanic ash. Furthermore, experiments in the Southern Ocean demonstrated significant phytoplankton community responses to volcanic ash supply in the absence of responses to addition of dissolved iron alone. At these sites, dissolved manganese concentrations were among the lowest ever measured in seawater, and we therefore suggest that the enhanced response to ash may have been a result of the relief of manganese (co)limitation. Our results imply that volcanic ash deposition events could trigger extensive phytoplankton blooms, potentially capable of significant impacts on regional carbon cycling.

Cyclical patterns of behaviour in timeseries of seismic and geodetic data at volcanoes are frequently observed during lava dome-building eruptions, and are particularly well-documented from the current eruption of the Soufriere Hills Volcano (SHV), Montserrat. However, the discontinuous nature of many SO 2 measurements often preclude the identification and quantitative analysis of cyclical patterns in degassing data. Here, using a long SO 2 timeseries from SHV, with continuous measurements since 2002, we explore for the first time degassing behaviour at a resolution comparable to that possible for seismic and deformation datasets. Timeseries analysis of flux data spanning 2002–2011 reveals that SO 2 emissions at SHV exhibit complex cyclicity, with dominant cycles evident on both multi-year and multi-week (~50 day) timescales. These cycles persist through phases of both active extrusion and eruptive pause, and show close similarities to periodic components previously identified at SHV in timeseries of seismicity, ground deformation and lava extrusion. The strength of expression or amplitude of degassing cycles, particularly on multi-week timescales, shows distinct temporal variation, and appears to correlate with the occurrence and nature of explosive activity occurring in 2002–2009. This suggests that the amplitude of surface gas flux cycles is modulated by physical conditions within the conduit. Direct quantitative comparison between seismicity, dome growth, and degassing for eruptive Phases 2 (2002–2003) and 3 (2005–2007) reveals that peaks in SO 2 flux appear to correspond broadly to enhanced lava extrusion and elevated seismicity within cycles of 30–50 days. However, time lags of 2, 4 and 7 days are observed between initial low-frequency seismic swarms and peaks in dome growth, SO 2 flux and rockfall event rate respectively. Multi-parameter correlations offer valuable insights into the controls on subsurface gas ascent, but further research is required to fully explore the contributions of permeability and overpressure, as well as other subsurface processes.

Caldera-forming eruptions of island volcanoes generate tsunamis by the interaction of different eruptive phenomena with the sea. Such tsunamis are a major hazard, but forward models of their impacts are limited by poor understanding of source mechanisms. The caldera-forming eruption of Santorini in the Late Bronze Age is known to have been tsunamigenic, and caldera collapse has been proposed as a mechanism. Here, we present bathymetric and seismic evidence showing that the caldera was not open to the sea during the main phase of the eruption, but was flooded once the eruption had finished. Inflow of water and associated landsliding cut a deep, 2.0–2.5 km3, submarine channel, thus filling the caldera in less than a couple of days. If, as at most such volcanoes, caldera collapse occurred syn-eruptively, then it cannot have generated tsunamis. Entry of pyroclastic flows into the sea, combined with slumping of submarine pyroclastic accumulations, were the main mechanisms of tsunami production., The Bronze Age eruption of Santorini is known to have generated tsunamis with caldera collapse as the likely mechanism. However, new bathymetric and seismic data presented by Nomikou et al. show that the entry of pyroclastic flows into the sea is the most likely tsunami-generating mechanism at Santorini.

EnVision is an ambitious but low-risk response to ESA's call for a medium-size mission opportunity for a launch in 2022. Venus is the planet most similar to Earth in mass, bulk properties and orbital distance, but has evolved to become extremely hostile to life. EnVision's 5-year mission objectives are to determine the nature of and rate of change caused by geological and atmospheric processes, to distinguish between competing theories about its evolution and to help predict the habitability of extrasolar planets. Three instrument suites will address specific surface, atmosphere and ionosphere science goals. The Surface Science Suite consists of a 2.2 m 2 radar antenna with Interferometer, Radiometer and Altimeter operating modes, supported by a complementary IR surface emissivity mapper and an advanced accelerometer for orbit control and gravity mapping. This suite will determine topographic changes caused by volcanic, tectonic and atmospheric processes at rates as low as 1 mm a -1. The Atmosphere Science Suite consists of a Doppler LIDAR for cloud top altitude, wind speed and mesospheric structure mapping, complemented by IR and UV spectrometers and a spectrophotopolarimeter, all designed to map the dynamic features and compositions of the clouds and middle atmosphere to identify the effects of volcanic and solar processes. The Ionosphere Science Suite uses a double Langmiur probe and vector magnetometer to understand the behaviour and long-term evolution of the ionosphere and induced magnetosphere. The suite also includes an interplanetary particle analyser to determine the delivery rate of water and other components to the atmosphere. © 2011 Springer Science+Business Media B.V.

Transient micronutrient enrichment of the surface ocean can enhance phytoplankton growth rates and alter microbial community structure with an ensuing spectrum of biogeochemical feedbacks. Strong phytoplankton responses to micronutrients supplied by volcanic ash have been reported recently. Here we: (i) synthesize findings from these recent studies; (ii) report the results of a new remote sensing study of ash fertilization; and (iii) calculate theoretical bounds of ash-fertilized carbon export. Our synthesis highlights that phytoplankton responses to ash do not always simply mimic that of iron amendment; the exact mechanisms for this are likely biogeochemically important but are not yet well understood. Inherent optical properties of ash-loaded seawater suggest rhyolitic ash biases routine satellite chlorophyll-a estimation upwards by more than an order of magnitude for waters with 0.5 mg chlorophyll-a m-3. For this reason post-ash-deposition chlorophyll-a changes in oligotrophic waters detected via standard Case 1 (open ocean) algorithms should be interpreted with caution. Remote sensing analysis of historic events with a bias less than a factor of 2 provided limited stand-alone evidence for ash-fertilization. Confounding factors were poor coverage, incoherent ash dispersal, and ambiguity ascribing biomass changes to ash supply over other potential drivers. Using current estimates of iron release and carbon export efficiencies, uncertainty bounds of ash-fertilized carbon export for 3 events are presented. Patagonian iron supply to the Southern Ocean from volcanic eruptions is less than that of windblown dust on thousand year timescales but can dominate supply at shorter timescales. Reducing uncertainties in remote sensing of phytoplankton response and nutrient release from ash are avenues for enabling assessment of the oceanic response to large-scale transient nutrient enrichment.

The 2014–2015 Bárðarbunga-Veiðivötn fissure eruption at Holuhraun produced about 1.5 km3 of lava, making it the largest eruption in Iceland in more than 200 years. Over the course of the eruption, daily volcanic sulfur dioxide (SO2) emissions exceeded daily SO2 emissions from all anthropogenic sources in Europe in 2010 by at least a factor of 3. We present surface air quality observations from across Northern Europe together with satellite remote sensing data and model simulations of volcanic SO2 for September 2014. We show that volcanic SO2 was transported in the lowermost troposphere over long distances and detected by air quality monitoring stations up to 2750 km away from the source. Using retrievals from the Ozone Monitoring Instrument (OMI) and the Infrared Atmospheric Sounding Interferometer (IASI), we calculate an average daily SO2 mass burden of 99 ± 49 kilotons (kt) of SO2 from OMI and 61 ± 18 kt of SO2 from IASI for September 2014. This volcanic burden is at least a factor of 2 greater than the average SO2 mass burden between 2007 and 2009 due to anthropogenic emissions from the whole of Europe. Combining the observational data with model simulations using the United Kingdom Met Office's Numerical Atmospheric-dispersion Modelling Environment model, we are able to constrain SO2 emission rates to up to 120 kilotons per day (kt/d) during early September 2014, followed by a decrease to 20–60 kt/d between 6 and 22 September 2014, followed by a renewed increase to 60–120 kt/d until the end of September 2014. Based on these fluxes, we estimate that the eruption emitted a total of 2.0 ± 0.6 Tg of SO2 during September 2014, in good agreement with ground-based remote sensing and petrological estimates. Although satellite-derived and model-simulated vertical column densities of SO2 agree well, the model simulations are biased low by up to a factor of 8 when compared to surface observations of volcanic SO2 on 6–7 September 2014 in Ireland. These biases are mainly due to relatively small horizontal and vertical positional errors in the simulations of the volcanic plume occurring over transport distances of thousands of kilometers. Although the volcanic air pollution episodes were transient and lava-dominated volcanic eruptions are sporadic events, the observations suggest that (i) during an eruption, volcanic SO2 measurements should be assimilated for near real-time air quality forecasting and (ii) existing air quality monitoring networks should be retained or extended to monitor SO2 and other volcanic pollutants., School of Earth and Environment (University of Leeds) UK Natural Environment Research Council (NERC) NE/I015612/1 Met Office Academic Partnership NERC NE/M021130/1 COMET

Tuffisite veins are glass-filled fractures formed when magma fragments during degassing within the conduit. These veins form transient channels through which exsolved gases can escape from magma. The purpose of this study is to determine the extent to which chemical heterogeneity within the melt results from gas transport, and assess how this can be used to study magma degassing. Two tuffisite veins from contrasting rhyolitic eruptions at Torfajökull (Iceland) and Chaitén (Chile) were studied in detail. The tuffisite vein from Torfajökull is from a shallow dissected conduit (~70. ka) that fed a degassed lava flow, while the sample from Chaitén was a bomb ejected during the waning phases of Plinian activity in May 2008. The results of detailed in situ chemical analyses (synchrotron XRF, FTIR, LA-ICP-MS) show that in both veins larger vesiculated fragments are enriched in volatile elements (Torfajökull: H, Li, Cl; Chaitén: Li, Cl, Cu, Zn, As, Sn, Sb) compared to the host, while the surrounding smaller particles are depleted in the Torfajökull vein (Li, Cl, Zn, Br, Rb, Pb), but enriched in the Chaitén vein (K, Cu, Zn, As, Mo, Sb, Pb). The lifespans of both veins and the fluxes of gas and particles through them can be estimated using diffusion profiles and enrichment factors. The Torfajökull vein had a longer lifespan (~a day) and low particle velocities (~cm/s), while the Chaitén vein was shorter lived (

Understanding the underlying structure of data from volcano monitoring is essential to identify precursors to changes in eruptive activity and to comprehend volcanic processes. However, effective analysis of longer-term trends in these signals is challenging as volcanic data are not necessarily statistically stationary or linear, particularly those from lava dome-forming volcanoes, which are commonly characterised by pulsatory eruptive activity. Here, we use detrended fluctuation analysis (DFA), a statistical technique previously applied to nonstationary data, to identify long-range (slowly decaying, e.g. power-law) correlations in a number of time-series of volcano seismicity recorded during the recent dome-forming eruptions of Volcán de Colima, Mexico, and Soufrière Hills Volcano, Montserrat. For all the time-series analysed, correlation strength varies through time and/or on different timescales; in some cases, this variation is periodic, seasonal, and/or related to activity. These results may provide new insights into eruptive processes and possibly further constrain the generation mechanisms of a number of the volcano-seismic event classes analysed. Furthermore, the correlation properties of real-time seismic measurements are shown (retrospectively) to contain information valuable to real-time volcano monitoring that is not identifiable by conventional analysis techniques. This study therefore demonstrates that long-range correlation analysis may be useful for extracting additional information from monitoring data at dome-forming or similar volcanoes. © 2013 Elsevier B.V.

Mt. Etna is a major natural source of Hg to the Mediterranean region. Total mercury concentrations, [Hg] tot, in Castanea sativa (sweet chestnut) leaves sampled 7-13km from Etna's vents (during six campaigns in 2005-2011) were determined using atomic absorption spectroscopy. [Hg] tot in C. sativa was greatest on Etna's SE flank reflecting Hg deposition from the typically overhead volcanic plume. [Hg] tot also showed Hg accumulation over the growing season, increasing with leaf age and recent eruptive activity. [Hg] tot in C. sativa was not controlled by [Hg] tot in soils, which instead was greatest on Etna's NW flank, and was correlated with the proportion of organic matter in the soil (% Org). An elevated [Hg] tot/% Org ratio in soils on Etna's SE flank is indicative of increased Hg deposition. This ratio was also found to decrease with local soil pH, suggesting that Hg deposited to the low pH and organic-poor soils on Etna's SE flank may not be retained but will instead be released to groundwater or re-emitted to the atmosphere. These results show that the deposition of volcanic Hg has clear impacts and confirm that Etna is an important source of Hg to the local environment. © 2012 Elsevier B.V.

International audience; Ir and Pt are siderophile elements that are considered proxies of meteoric material of cosmic origin entrapped within polar ice layers. However, volcanic and anthropogenic fallouts have the potential to perturb their characteristic extraterrestrial signature even in remote polar areas. Here we show a record of Ir and Pt concentrations in snow samples collected from a 2.7 m pit, which was dug at Summit (Central Greenland), and covered five years from winter 1991 to summer 1995. A well-defined peak of Pt, and a spike of Ir, were found at the base of the snow pit record. These maxima occur in close concurrence with large concentration peaks in Al, Ag, Cd and Hg. Dating of the snow layers together with some geochemical evidence suggests that these peaks originated from the fallout to Greenland of volcanic ash emitted by the nearby Hekla volcano (Iceland), during the eruption of January–March 1991. Interestingly, an anomalous peak of methane sulfonic acid (MSA) in Greenland snow also corresponds to the Hekla ash fallout. This might point to an early biomass production in the North Atlantic Ocean during the first half of 1991, which was possibly stimulated by the fertilizing action of the Hekla ash fallout to seawater. During the following years (1992–1995) the global atmosphere was under the influence of the large perturbation produced by the eruption of Mt. Pinatubo (Philippines) in June 1991. Relatively high Ir and Pt concentrations with super-chondritic ratios are recorded especially during summer 1993. We discuss if this can be interpreted as the possible stratospheric input of Pinatubo's aerosol or fallout of extraterrestrial origin. During the same period the snow pit record was also influenced by the advection of air masses enriched in Pt with respect to Ir. One possibility is that this additional Pt contribution originated from widespread emissions into the troposphere produced by vehicles equipped with catalytic converters. In any case, Pt concentration levels found in recent Greenland snow are about two orders of magnitude lower than previously thought, pointing to a much lower anthropogenic contamination of the Arctic regions from Pt. This challenges the concept of an important hemispheric contamination of Pt from vehicles equipped with catalytic converters.

Extremely voluminous magmatic systems known as large igneous provinces (LIPs) punctuate Earth’s history, and the gases they release plausibly link large-scale geodynamic and magmatic processes with major climate shifts in Earth’s geological record. However, quantifying the relationships between magmatism, gas release and environmental changes remains challenging. In this Review, we explore the major insights and outstanding questions regarding the linked evolution of mantle melting, expansive magmatic systems and the redistribution of volatiles from the solid Earth to the atmosphere. The evolution of mantle melt generation during LIP episodes sets the fundamental tempo of magma emplacement throughout the crust. The progression of crustal LIP magmatism and associated hydrothermal activity help shape the chemical evolution of the continental lithosphere and surface environment. Percolation of magmatic and metamorphic volatiles can decouple the tempo of gas release — a potential key driver of environmental changes — from the tempo of extrusive volcanic activity. LIPs demonstrate how large-scale magmatic systems interact with the surrounding lithosphere to propel evolving regimes of magma and volatile transfer through the crust. New, temporally resolved constraints on the evolution of LIP plumbing systems are needed to keep pace with increasingly precise timelines of palaeoenvironmental change during LIP emplacement. Major environmental disruptions throughout Earth’s history are often linked to extensive magmatic events, termed large igneous provinces. This Review explores the coupled evolution of mantle melting, magmatism and volatile release over the life cycle of large igneous provinces.

This work is a contribution to the Natural Environment Research Council (NERC) funded RiftVolc project (NE/L013932/1, Rift volcanism: past, present, and future). W.H., T.A.M., and D.M.P. are supported by and contribute to the NERC Centre for the Observation and Modelling of Earthquakes, Volcanoes, and Tectonics (COMET). W.H. M.J.S. were supported by a NERC studentships NE/J5000045/1 and NE/K500811/01 respectively. The Main Ethiopian Rift hosts a number of peralkaline volcanic centres, with many showing signs of recent unrest. Due, in part, to the low number of historical eruptions recorded in the region, volcanism in the Main Ethiopian Rift remains understudied relative to other volcanic settings and conditions of magma storage remain almost entirely unknown. Aluto is one of these restless caldera systems and identifying magma storage conditions is vital for evaluating the risks posed by recent periods of unrest. In this study, we ran ~ 150 fractional crystallisation models, using the Rhyolite-MELTS thermodynamic software, within the range P = 50–300 MPa, starting H2O = 0.5–3 wt% and fO2 = QFM-2 − QFM + 1. This represents a realistic range of potential magma storage conditions at Aluto. We assessed the fractionation trends produced using two different starting compositions, which represent different estimates of the parental melt feeding the system. The predicted liquid lines of descent produced by these models are compared with Aluto whole-rock data from the literature, and are presented along with new observations of the natural phase assemblage and erupted mineral compositions to provide information on the magma storage conditions. Using a new, quantitative statistical approach to compare empirical data and thermodynamic model-outputs, we find that the compositions of evolved peralkaline rhyolites from Aluto are best reproduced by isobaric fractional crystallisation from a rift-related basaltic composition, without the need for significant crustal assimilation. Around 90% protracted fractional crystallisation is required to produce these compositions. This indicates that the magmatic system is likely to exist as a highly crystalline mush. The best agreement between models and natural samples is at low pressures (150 MPa), low initial H2O concentrations (0.5 wt%) and relatively high oxygen fugacity (QFM). The depth of magma storage derived from these results (~ 5.6 ± 1 km) agrees well with the source depths modelled from measured ground deformation at Aluto in 2008. Data from other peralkaline volcanic centres in the Main Ethiopian Rift, such as Boset and Gedemsa, and at other locations globally (e.g. Pantelleria, Italy) suggest that these storage conditions are a common feature of many peralkaline volcanic centres. Our data is consistent with the formation of a Daly Gap at Aluto due to compositional stratification of the magma reservoir beneath the caldera, and the non-linear relationship between temperature and SiO2 concentration during magmatic differentiation. Postprint

Records suggest that the Permo–Triassic mass extinction (PTME) involved one of the most severe terrestrial ecosystem collapses of the Phanerozoic. However, it has proved difficult to constrain the extent of the primary productivity loss on land, hindering our understanding of the effects on global biogeochemistry. We build a new biogeochemical model that couples the global Hg and C cycles to evaluate the distinct terrestrial contribution to atmosphere–ocean biogeochemistry separated from coeval volcanic fluxes. We show that the large short-lived Hg spike, and nadirs in δ202Hg and δ13C values at the marine PTME are best explained by a sudden, massive pulse of terrestrial biomass oxidation, while volcanism remains an adequate explanation for the longer-term geochemical changes. Our modelling shows that a massive collapse of terrestrial ecosystems linked to volcanism-driven environmental change triggered significant biogeochemical changes, and cascaded organic matter, nutrients, Hg and other organically-bound species into the marine system., The environmental changes at the Permian–Triassic boundary are thought to have been caused primarily by volcanic eruptions. Here the authors develop a model to show that the loss of ecosystems on land and consequent massive terrestrial biomass oxidation triggered large biogeochemical changes in the oceans at the time of the marine mass extinction.