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Author

Emily Mason

Bio: Emily Mason is an academic researcher from University of Cambridge. The author has contributed to research in topics: Volcano & Plume. The author has an hindex of 5, co-authored 9 publications receiving 186 citations.
Topics: Volcano, Plume, Geology, Volcanic Gases, Outgassing

Papers
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Journal ArticleDOI
21 Jul 2017-Science
TL;DR: The carbon isotope composition of mean global volcanic gas is considerably heavier, at -3.8 to -4.6 per mil (m) than the canonical mid-ocean ridge basalt value of -6.0 m as discussed by the authors.
Abstract: 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.

135 citations

Journal ArticleDOI
TL;DR: In this article, the authors compare UAS-derived gas timeseries to simultaneous crater rim multi-GAS data and UV camera imagery to investigate early plume evolution, and observe good agreement between time-averaged molar gas ratios obtained from simultaneous UAS and ground-based multiGAS acquisitions, and conclude that UAS measurements made in the young, less diluted plume reveal additional short-term periodic structure that reflects active degassing through discrete, audible gas exhalations.
Abstract: Volcanic gas emissions are intimately linked to the dynamics of magma ascent and outgassing, and, on geological timescales, constitute an important source of volatiles to the Earth's atmosphere. Measurements of gas composition and flux are therefore critical to both volcano monitoring and to determining the contribution of volcanoes to global geochemical cycles. However, significant gaps remain in our global inventories of volcanic emissions, (particularly for CO2, which requires proximal sampling of a concentrated plume) for those volcanoes where the near‐vent region is hazardous or inaccessible. Unmanned Aerial Systems (UAS) provide a robust and effective solution to proximal sampling of dense volcanic plumes in extreme volcanic environments. Here, we present gas compositional data acquired using a gas sensor payload aboard a UAS flown at Volcan Villarrica, Chile. We compare UAS‐derived gas timeseries to simultaneous crater rim multi‐GAS data and UV camera imagery to investigate early plume evolution. SO2 concentrations measured in the young proximal plume exhibit periodic variations that are well‐correlated with the concentrations of other species. By combining molar gas ratios (CO2/SO2 = 1.48–1.68, H2O/SO2 = 67–75 and H2O/CO2 = 45–51) with the SO2 flux (142 ± 17 t/day) from UV camera images, we derive CO2 and H2O fluxes of ~150 t/day and ~2850 t/day, respectively. We observe good agreement between time‐averaged molar gas ratios obtained from simultaneous UAS‐ and ground‐based multi‐GAS acquisitions. However, the UAS measurements made in the young, less diluted plume reveal additional short‐term periodic structure that reflects active degassing through discrete, audible gas exhalations.

46 citations

Journal ArticleDOI
TL;DR: In this article, a time series of carbon fluxes into and out of the Earth's interior through the past 200 million years is used to compare the relative importance of different tectonic settings throughout Earth's history to carbon outgassing.
Abstract: Carbon is a key control on the surface chemistry and climate of Earth. Significant volumes of carbon are input to the oceans and atmosphere from deep Earth in the form of degassed CO2 and are returned to large carbon reservoirs in the mantle via subduction or burial. Different tectonic settings (e.g., volcanic arcs, mid-ocean ridges, and continental rifts) emit fluxes of CO2 that are temporally and spatially variable, and together they represent a first-order control on carbon outgassing from the deep Earth. A change in the relative importance of different tectonic settings throughout Earth’s history has therefore played a key role in balancing the deep carbon cycle on geological timescales. Over the past 10 years the Deep Carbon Observatory has made enormous progress in constraining estimates of carbon outgassing flux at different tectonic settings. Using plate boundary evolution modeling and our understanding of present-day carbon fluxes, we develop time series of carbon fluxes into and out of the Earth’s interior through the past 200 million years. We highlight the increasing importance of carbonate-intersecting subduction zones over time to carbon outgassing, and the possible dominance of carbon outgassing at continental rift zones, which leads to maxima in outgassing at 130 and 15 Ma. To a first-order, carbon outgassing since 200 Ma may be net positive, averaging ∼50 Mt C yr–1 more than the ingassing flux at subduction zones. Our net outgassing curve is poorly correlated with atmospheric CO2, implying that surface carbon cycling processes play a significant role in modulating carbon concentrations and/or there is a long-term crustal or lithospheric storage of carbon which modulates the outgassing flux. Our results highlight the large uncertainties that exist in reconstructing the corresponding in- and outgassing fluxes of carbon. Our synthesis summarizes our current understanding of fluxes at tectonic settings and their influence on atmospheric CO2, and provides a framework for future research into Earth’s deep carbon cycling, both today and in the past.

37 citations

Journal ArticleDOI
TL;DR: It is found that aerial strategies reduce uncertainties associated with ground-based remote sensing of SO2 flux and enable near–real-time measurements of plume chemistry and carbon isotope composition and the need to account for time averaging of temporal variability in volcanic gas emissions in global flux estimates is emphasized.
Abstract: Volcanic emissions are a critical pathway in Earth’s carbon cycle. Here, we show that aerial measurements of volcanic gases using unoccupied aerial systems (UAS) transform our ability to measure and monitor plumes remotely and to constrain global volatile fluxes from volcanoes. Combining multi-scale measurements from ground-based remote sensing, long-range aerial sampling, and satellites, we present comprehensive gas fluxes—3760 ± [600, 310] tons day−1 CO2 and 5150 ± [730, 340] tons day−1 SO2—for a strong yet previously uncharacterized volcanic emitter: Manam, Papua New Guinea. The CO2/ST ratio of 1.07 ± 0.06 suggests a modest slab sediment contribution to the sub-arc mantle. We find that aerial strategies reduce uncertainties associated with ground-based remote sensing of SO2 flux and enable near–real-time measurements of plume chemistry and carbon isotope composition. Our data emphasize the need to account for time averaging of temporal variability in volcanic gas emissions in global flux estimates.

28 citations

Journal ArticleDOI
TL;DR: In this paper, the authors analyzed 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 (SO2) between 2007 and 2018 and PM2.5 (aerosol particulate matter with diameter < 2.5 μm) between 2010 and 2018.
Abstract: 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 (SO2) between 2007 and 2018 and PM2.5 (aerosol particulate matter with diameter <2.5 μm) between 2010 and 2018. Additional air quality data were collected through a community-operated network of low-cost PM2.5 sensors during the 2018 LERZ eruption. From 2007 to 2018 the two most significant escalations in Kīlauea's volcanic emissions were: the summit eruption that began in 2008 (Kīlauea emissions averaged 5–6 kt/day SO2 from 2008 until summit activity decreased in May 2018) and the LERZ eruption in 2018 when SO2 emission rates reached a monthly average of 200 kt/day during June. In this paper we focus on characterizing the airborne pollutants arising from the 2018 LERZ eruption and the spatial distribution and severity of volcanic air pollution events across the Island of Hawai'i. The LERZ eruption caused the most frequent and severe exceedances of the Environmental Protection Agency (EPA) PM2.5 air quality threshold (35 μg/m3 as a daily average) in Hawai'i in the period 2010–2018. In Kona, for example, the maximum 24-h-mean mass concentration of PM2.5 was recorded as 59 μg/m3 on the twenty-ninth of May 2018, which was one of eight recorded exceedances of the EPA air quality threshold during the 2018 LERZ eruption, where there had been no exceedances in the previous 8 years as measured by the HDOH and NPS networks. SO2 air pollution during the LERZ eruption was most severe in communities in the south and west of the island, as measured by selected HDOH and NPS stations in this study, with a maximum 24-h-mean mass concentration of 728 μg/m3 recorded in Ocean View (100 km west of the LERZ emission source) in May 2018. Data from the low-cost sensor network correlated well with data from the HDOH PM2.5 instruments, confirming that these low-cost sensors provide a robust means to augment reference-grade instrument networks.

20 citations


Cited by
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01 Dec 2002
TL;DR: In this paper, the authors estimate that half to two thirds of subducted crustal water is later refluxed at the prism toe; most of the remaining water escapes at subarc depths, triggering partial melting.
Abstract: [1] The alteration of upper oceanic crust entails growth of hydrous minerals and loss of macroporosity, with associated large-scale fluxes of H2O, CO2, Cl−, and K2O between seawater and crust. This age-dependent alteration can be quantified by combining a conceptual alteration model with observed age-dependent changes in crustal geophysical properties at DSDP/ODP sites, permitting estimation of crustal concentrations of H2O, CO2, Cl−, and K2O, given crustal age. Surprisingly, low-temperature alteration causes no net change in total water; pore water loss is nearly identical to bound water gain. Net change in total crustal K2O is also smaller than expected; the obvious low-temperature enrichment is partly offset by earlier high-temperature depletion, and most crustal K2O is primary rather than secondary. I calculate crustal concentrations of H2O, CO2, Cl−, and K2O for 41 modern subduction zones, thereby determining their modern mass fluxes both for individual subduction zones and globally. This data set is complemented by published flux determinations for subducting sediments at 26 of these subduction zones. Global mass fluxes among oceans, oceanic crust, continental crust, and mantle are calculated for H2O, Cl−, and K2O. Except for the present major imbalance between sedimentation and sediment subduction, most fluxes appear to be at or near steady state. I estimate that half to two thirds of subducted crustal water is later refluxed at the prism toe; most of the remaining water escapes at subarc depths, triggering partial melting. The flux of subducted volatiles, however, does not appear to correlate with either rate of arc magma generation or magnitude of interplate earthquakes.

251 citations

Journal ArticleDOI
01 Jun 2020
TL;DR: In this paper, the authors examined the mechanisms of carbon exchange between rocks and the atmosphere, and discussed the balance of CO2 sources and sinks, and demonstrated that organic carbon burial and oxidative weathering, not widely considered in most models, control the net CO2 budget associated with erosion.
Abstract: Mountain building results in high erosion rates and the interaction of rocks with the atmosphere, water and life. Carbon transfers that result from increased erosion could control the evolution of Earth’s long-term climate. For decades, attention has focused on the hypothesized role of mountain building in drawing down atmospheric carbon dioxide (CO2) via silicate weathering. However, it is now recognized that mountain building and erosion affect the carbon cycle in other important ways. For example, erosion mobilizes organic carbon (OC) from terrestrial vegetation, transferring it to rivers and sediments, and thereby acting to draw down atmospheric CO2 in tandem with silicate weathering. Meanwhile, exhumation of sedimentary rocks can release CO2 through the oxidation of rock OC and sulfide minerals. In this Review, we examine the mechanisms of carbon exchange between rocks and the atmosphere, and discuss the balance of CO2 sources and sinks. It is demonstrated that OC burial and oxidative weathering, not widely considered in most models, control the net CO2 budget associated with erosion. Lithology strongly influences the impact of mountain building on the global carbon cycle, with an orogeny dominated by sedimentary rocks, and thus abundant rock OC and sulfides, tending towards being a CO2 source. By increasing erosion, mountain building can steer the evolution of atmospheric carbon dioxide (CO2) and global climate. This Review expands from the canonical focus on silicate weathering to consider the net carbon budget of erosion, including both CO2 sinks (silicate weathering, organic-carbon burial) and CO2 sources (oxidative weathering).

146 citations

Journal ArticleDOI
TL;DR: A comprehensive, structured and updated review of the field of chemical sensing using small drones, which exhaustively review current and emerging applications of this technology, as well as sensing platforms and algorithms developed by research groups and companies for tasks such as gas concentration mapping, source localization, and flux estimation.

96 citations

Journal ArticleDOI
TL;DR: In this paper, the authors explore the consequences and implications of such a volatile phase for petrogenesis and the fluid dynamics of magma reservoirs, and discuss the accumulation of the exsolved volatile phase at the roof zones of crystal-rich reservoirs for the large gas emissions observed during explosive eruptions, and for the development of metal-rich porphyry deposits.

88 citations

Journal ArticleDOI
TL;DR: In this paper, the authors investigated the effect of gas injection on the stability and chemical evolution of subvolcanic systems and found that CO2 flushing is a widespread process in both felsic and mafic systems.

85 citations