Search

Recent Icelandic rifting events have illuminated the roles of centralized crustal magma reservoirs and lateral magma transport1–4, important characteristics of mid-ocean ridge magmatism1,5. A consequence of such shallow crustal processing of magmas4,5 is the overprinting of signatures that trace the origin, evolution and transport of melts in the uppermost mantle and lowermost crust6,7. Here we present unique insights into processes occurring in this zone from integrated petrologic and geochemical studies of the 2021 Fagradalsfjall eruption on the Reykjanes Peninsula in Iceland. Geochemical analyses of basalts erupted during the first 50 days of the eruption, combined with associated gas emissions, reveal direct sourcing from a near-Moho magma storage zone. Geochemical proxies, which signify different mantle compositions and melting conditions, changed at a rate unparalleled for individual basaltic eruptions globally. Initially, the erupted lava was dominated by melts sourced from the shallowest mantle but over the following three weeks became increasingly dominated by magmas generated at a greater depth. This exceptionally rapid trend in erupted compositions provides an unprecedented temporal record of magma mixing that filters the mantle signal, consistent with processing in near-Moho melt lenses containing 107–108 m3 of basaltic magma. Exposing previously inaccessible parts of this key magma processing zone to near-real-time investigations provides new insights into the timescales and operational mode of basaltic magma systems.

Aerial measurements using unoccupied aerial systems (UAS) transform our ability to measure and monitor volcanic plumes., 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.

Here, we present the first ultraviolet (UV) camera measurements of sulphur dioxide (SO2) flux from Yasur volcano, Vanuatu, for the period 6–9 July 2018. These data yield the first direct gas-measurement-derived calculations of explosion gas masses at Yasur. Yasur typically exhibits persistent passive gas release interspersed with frequent Strombolian explosions. We used compact forms of the “PiCam” Raspberry Pi UV camera system [1,2] powered through solar panels to collect images. Our daily median SO2 fluxes ranged from 4 to 5.1 kg s−1, with a measurement uncertainty of −12.2% to +14.7%, including errors from the gas cell calibration drift, uncertainties in plume direction and distance, and errors from the plume velocity. This work highlights the use of particle image velocimetry (PIV) for plume velocity determination, which was preferred over the typically used cross-correlation and optical flow methods because of the ability to function over a variety of plume conditions. We calculated SO2 masses for Strombolian explosions ranging 8–81 kg (mean of 32 kg), which to our knowledge is the first budget of explosive gas masses from this target. Through the use of a simple statistical measure using the moving minimum, we estimated that passive degassing is the dominant mode of gas emission at Yasur, supplying an average of ~69% of the total gas released. Our work further highlights the utility of UV camera measurements in volcanology, and particularly the benefit of the multiple camera approach in error characterisation. This work also adds to our inventory of gas-based data, which can be used to characterise the spectrum of Strombolian activity across the globe.

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 Volcán 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.