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Many of the standard volcanic gas flux measurement approaches involve absorption spectroscopy in combination with wind speed measurements. Here, we present a new method using video images of volcanic plumes to measure the speed of convective structures combined with classical plume theory to estimate volcanic fluxes. We apply the method to a nearly vertical gas plume at Villarrica Volcano, Chile, and a wind-blown gas plume at Mount Etna, Italy. Our estimates of the gas fluxes are consistent in magnitude with previous reported fluxes obtained by spectroscopy and electrochemical sensors for these volcanoes. Compared to conventional gas flux measurement techniques focusing on SO2, our new model also has the potential to be used for sulfur-poor plumes in hydrothermal systems because it estimates the H2O flux.
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Basaltic open vent volcanoes are major global sources of volcanic gases. Many of these volcanoes outgas via intermittent Strombolian-type explosions separated by periods of passive degassing. The gas emitted during the explosions has high molar CO2/SO2 and SO2/HCl ratios, while during the passive degassing these ratios are lower. We present new laboratory experiments in a model volcanic conduit, which suggest that these differences in gas geochemistry are a consequence of gas migration through crystal-rich magma. We show that gas may flow along channels through the particle-laden liquid and, at a critical depth, the gas may displace an overlying crystal-rich plug en masse, producing a growing slug of gas. Owing to the friction on the walls of the conduit, this plug becomes progressively sheared and weakened until gas enriched in the least soluble volatiles breaks through, causing an explosion at the surface. When the gas slug bursts, liquid is drawn up in its wake, which exsolves the more soluble volatile components, which then vent passively at the surface until the next explosive slug-bursting event.
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Distorted olivines of enigmatic origin are ubiquitous in erupted products from a wide range of volcanic systems (e.g., Hawai'i, Iceland, Andes). Investigation of these features at Kilauea Volcano, Hawai'i, using an integrative crystallographic and chemical approach places quantitative constraints on mush pile thicknesses. Electron backscatter diffraction (EBSD) reveals that the microstructural features of distorted olivines, whose chemical composition is distinct from undistorted olivines, are remarkably similar to olivines within deformed mantle peridotites, but inconsistent with an origin from dendritic growth. This, alongside the spatial distribution of distorted grains and the absence of adcumulate textures, suggests that olivines were deformed within melt-rich mush piles accumulating within the summit reservoir. Quantitative analysis of subgrain geometry reveals that olivines experienced differential stresses of â¼3-12 MPa, consistent with their storage in mush piles with thicknesses of a few hundred metres. Overall, our microstructural analysis of erupted crystals provides novel insights into mush-rich magmatic systems.
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Olivine-hosted melt inclusions are commonly used to determine pre-eruptive storage conditions. However, this approach relies on the assumption that co-erupted olivines have a simple association with their carrier melts. We show that primitive olivine crystal cargoes and their melt inclusions display a high degree of geochemical disequilibrium with their carrier melts at Kilauea Volcano, Hawai'i. Within a given eruption, melt inclusions trapped in primitive olivine crystals exhibit compositional diversity exceeding that in erupted lava compositions since 1790 CE. This demonstrates that erupting liquids scavenge crystal cargoes from mush piles accumulating diverse melt inclusion populations over timescales of centuries or longer. Entrainment of hot primitive olivines into cooler, evolved carrier melts drives post-entrapment crystallization and sequestration of CO2 into vapour bubbles, producing spurious barometric estimates. While scavenged melt inclusion records may not be suitable for the investigation of eruption-specific processes, they record timescales of crystal storage and remobilization within magmatic mush piles.
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This introductory article provides a synopsis of our current understanding of the form and dynamics of magma reservoirs in the crust. This knowledge is based on a range of experimental, observational and theoretical approaches, some of which are multidisclipinary and pioneering. We introduce and provide a contextual background for the papers in this issue, which cover a wide range of topics, encompassing magma storage, transport, behaviour and rheology, as well as the timescales on which magma reservoirs operate. We summarize the key findings that emerged from the meeting and the challenges that remain. The study of magma reservoirs has wide implications not only for understanding geothermal and magmatic systems, but also for natural oil and gas reservoirs and for ore deposit formation. This article is part of the Theo Murphy meeting issue 'Magma reservoir architecture and dynamics'.
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We use both seismology and geobarometry to investigate the movement of melt through the volcanic crust of Iceland. We have captured melt in the act of moving within or through a series of sills ranging from the upper mantle to the shallow crust by the clusters of small earthquakes it produces as it forces its way upward. The melt is injected not just beneath the central volcanoes, but also at discrete locations along the rift zones and above the centre of the underlying mantle plume. We suggest that the high strain rates required to produce seismicity at depths of 10-25 km in a normally ductile part of the Icelandic crust are linked to the exsolution of carbon dioxide from the basaltic melts. The seismicity and geobarometry provide complementary information on the way that the melt moves through the crust, stalling and fractionating, and often freezing in one or more melt lenses on its way upwards: the seismicity shows what is happening instantaneously today, while the geobarometry gives constraints averaged over longer time scales on the depths of residence in the crust of melts prior to their eruption. This article is part of the Theo Murphy meeting issue 'Magma reservoir architecture and dynamics'.
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The trans-crustal magma system paradigm is forcing us to re-think processes responsible for magma evolution and eruption. A key concept in petrology is the liquid line of descent (LLD), which relates a series of liquids derived from a single parent, and therefore tracks the inverse of the crystallization path. It is common practice to attribute multiple magma compositions, and/or multiple melt compositions (from melt inclusions and matrix glass), to a single LLD. However, growing evidence for rapid, and often syn-eruptive, assembly of multiple magma components (crystals and melts) from different parts of a magmatic system suggests that erupted magma and melt compositions will not necessarily represent a single LLD, but instead may reflect the multiple paths in pressure-temperature space. Here, we use examples from mafic magmatic systems in both ocean island and arc settings to illustrate the range of melt compositions present in erupted samples, and to explore how they are generated, and how they interact. We highlight processes that may be deduced from mafic melt compositions, including the mixing of heterogeneous primitive liquids from the mantle, pre-eruptive magma storage at a range of crustal and sub-Moho depths, and syn-eruptive mixing of melts generated from these storage regions. The relative dominance of these signatures in the glasses depends largely on the water content of the melts. We conclude that preserved melt compositions provide information that is complementary to that recorded by the volatile contents of crystal-hosted melt inclusions and coexisting mineral compositions, which together can be used to address questions about both the pre- and syn-eruptive state of volcanic systems. This article is part of the Theo Murphy meeting issue 'Magma reservoir architecture and dynamics'.
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Strombolian volcanic explosions are commonly attributed to the rise and burst of conduit-filling gas slugs. The magmas associated with strombolian activity, however, are typically not only volatile-rich but also highly crystalline, with mush regions in the shallow plumbing system, where an exsolved volatile phase may also be abundant. Through analogue experiments, we explore a new mechanism to form gas slugs and strombolian explosions. A steady flux of gas is supplied to the base of a particle-rich liquid layer, generating a localised gas intrusion, which initially grows through plastic deformation. Once the pressure in the intrusion overcomes the effective tensile strength of the particle pack, a localised channel opens, allowing gas to propagate upwards. As the pressure in the intrusion falls, the gas pocket collapses. The continued supply of gas leads to the formation of a new intrusion, and the cycle repeats. With higher gas fluxes, continuous channelised gas flow occurs. Highly crystalline shallow portions of basaltic conduits may act as a flow valve, transforming a steady gas flux into a series of discrete gas slugs which cause explosions.
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The flux of carbon into and out of Earth's surface environment has implications for Earth's climate and habitability. We compiled a global data set for carbon and helium isotopes from volcanic arcs and demonstrated that the carbon isotope composition of mean global volcanic gas is considerably heavier, at -3.8 to -4.6 per mil (), than the canonical mid-ocean ridge basalt value of -6.0. The largest volcanic emitters outgas carbon with higher δ13C and are located in mature continental arcs that have accreted carbonate platforms, indicating that reworking of crustal limestone is an important source of volcanic carbon. The fractional burial of organic carbon is lower than traditionally determined from a global carbon isotope mass balance and may have varied over geological time, modulated by supercontinent formation and breakup.
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Observations of volcanoes from space are a critical component of volcano monitoring, but we lack quantitative integrated models to interpret them. The atmospheric sulfur yields of eruptions are variable and not well correlated with eruption magnitude and for many eruptions the volume of erupted material is much greater than the subsurface volume change inferred from ground displacements. Up to now, these observations have been treated independently, but they are fundamentally linked. If magmas are vapour-saturated before eruption, bubbles cause the magma to become more compressible, resulting in muted ground displacements. The bubbles contain the sulfur-bearing vapour injected into the atmosphere during eruptions. Here we present a model that allows the inferred volume change of the reservoir and the sulfur mass loading to be predicted as a function of reservoir depth and the magma's oxidation state and volatile content, which is consistent with the array of natural data.
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Magma degassing plays a fundamental role in controlling the style of volcanic eruptions. Whether a volcanic eruption is explosive, or effusive, is of crucial importance to approximately 500 million people living in the shadow of hazardous volcanoes worldwide. Studies of how gases exsolve and separate from magma prior to and during eruptions have been given new impetus by the emergence of more accurate and automated methods to measure volatile species both as volcanic gases and dissolved in the glasses of erupted products. The composition of volcanic gases is dependent on a number of factors, the most important being magma composition and the depth of gas-melt segregation prior to eruption; this latter parameter has proved difficult to constrain in the past, yet is arguably the most critical for controlling eruptive style. Spectroscopic techniques operating in the infrared have proved to be of great value in measuring the composition of gases at high temporal resolution. Such methods, when used in tandem with microanalytical geochemical investigations of erupted products, are leading to better constraints on the depth at which gases are generated and separated from magma. A number of recent studies have focused on transitions between explosive and effusive activity and have led to a better understanding of gas-melt segregation at basaltic volcanoes. Other studies have focused on degassing during intermediate and silicic eruptions. Important new results include the recognition of fluxing by deep-derived gases, which buffer the amount of dissolved volatiles in the melt at shallow depths, and the observation of gas flow up permeable conduit wall shear zones, which may be the primary mechanism for gas loss at the cusp of the most explosive and unpredictable volcanic eruptions. In this paper, I review current and future directions in the field of geochemical studies of volcanic degassing processes and illustrate how the new insights are beginning to change the way in which we understand and classify volcanic eruptions.