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Submarine slope failures occur at all continental margins, but the processes generating different mass wasting phenomena remain poorly understood. Multibeam bathymetry mapping of the Middle America Trench reveals numerous continental slope failures of different dimensions and origin. For example, large rotational slumps have been interpreted to be caused by slope collapse in the wake of subducting seamounts. In contrast, the mechanisms generating translational slides have not yet been described. Lithology, shear strength measurements, density, and pore water alkalinity from a sediment core across a slide plane indicate that a few centimeters thick intercalated volcanic tephra layer marks the detachment surface. The ash layer can be correlated to the San Antonio tephra, emplaced by the 6000 year old caldera‐forming eruption from Masaya‐Caldera, Nicaragua. The distal deposits of this eruption are widespread along the continental slope and ocean plate offshore Nicaragua. Grain size measurements permit us to estimate the reconstruction of the original ash layer thickness at the investigated slide. Direct shear test experiments on Middle American ashes show a high volume reduction during shearing. This indicates that marine tephra layers have the highest hydraulic conductivity of the different types of slope sediment, enabling significant volume reduction to take place under undrained conditions. This makes ash layers mechanically distinct within slope sediment sequences. Here we propose a mechanism by which ash layers may become weak planes that promote translational sliding. The mechanism implies that ground shaking by large earthquakes induces rearrangement of ash shards causing their compaction (volume reduction) and produces a rapid accumulation of water in the upper part of the layer that is capped by impermeable clay. The water‐rich veneer abruptly reduces shear strength, creating a detachment plane for translational sliding. Tephra layers might act as slide detachment planes at convergent margins of subducting zones, at submarine slopes of volcanic islands, and at submerged volcano slopes in lakes.

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Barren Island (Andaman Sea) is the northernmost active volcano of the Indonesian Arc. To construct the eruptive history of this little studied volcano, we measured 14 C dates of inorganic carbon in sediment beds, and Sr and Nd isotopic ratios of seven discrete ash layers, in a marine sediment core collected from 32 km southeast of the volcano. The study reveals that the volcano had seven major ash eruptions at ~70, 69, 61, 24, 19, 15, and 10 ka. The ash layers erupted from 70 ka through 19 ka have highly uniform Nd isotopic composition, and since the ~15 ka eruption to the present the isotopic composition has been highly variable. Between ~24 ka and ~10 ka, the volcano had large ash eruptions spaced at 4,500 year intervals. Isotopically correlating the precaldera lavas and ash exposed on the volcano to the uppermost ash layer in the core, we infer that the caldera of Barren Island volcano is younger than 10 ka.

There is a temporal correlation between the peak activity of the North Atlantic Igneous Province (NAIP) and the Paleocene–Eocene Thermal Maximum (PETM), suggesting that the NAIP may have initiated and/or prolonged this extreme warming event. However, corroborating a causal relationship is hampered by a scarcity of expanded sedimentary records that contain both climatic and volcanic proxies. One locality hosting such a record is the island of Fur in Denmark, where an expanded pre- to post-PETM succession containing hundreds of NAIP ash layers is exceptionally well preserved. We compiled a range of environmental proxies, including mercury (Hg) anomalies, paleotemperature proxies, and lithium (Li) and osmium (Os) isotopes, to trace NAIP activity, hydrological changes, weathering, and seawater connectivity across this interval. Volcanic proxies suggest that NAIP activity was elevated before the PETM and appears to have peaked during the body of the δ13C excursion but decreased considerably during the PETM recovery. This suggests that the acme in NAIP activity, dominated by flood basalt volcanism and thermogenic degassing from contact metamorphism, was likely confined to just ∼ 200 kyr (ca. 56.0–55.8 Ma). The hundreds of thick (> 1 cm) basaltic ashes in the post-PETM strata likely represent a change from effusive to explosive activity, rather than an increase in NAIP activity. Detrital δ7Li values and clay abundances suggest that volcanic ash production increased the basaltic reactive surface area, likely enhancing silicate weathering and atmospheric carbon sequestration in the early Eocene. Signals in lipid biomarkers and Os isotopes, traditionally used to trace paleotemperature and weathering changes, are used here to track seaway connectivity. These proxies indicate that the North Sea was rapidly cut off from the North Atlantic in under 12 kyr during the PETM recovery due to NAIP thermal uplift. Our findings reinforce the hypothesis that the emplacement of the NAIP had a profound and complex impact on Paleocene–Eocene climate, both directly through volcanic and thermogenic degassing and indirectly by driving regional uplift and changing seaway connectivity.

Airborne lidar and in-situ measurements of aerosols and trace gases were performed in volcanic ash plumes over Europe between Southern Germany and Iceland with the Falcon aircraft during the eruption period of the Eyjafjalla volcano between 19 April and 18 May 2010. Flight planning and measurement analyses were supported by a refined Meteosat ash product and trajectory model analysis. The volcanic ash plume was observed with lidar directly over the volcano and up to a distance of 2700 km downwind, and up to 120 h plume ages. Aged ash layers were between a few 100 m to 3 km deep, occurred between 1 and 7 km altitude, and were typically 100 to 300 km wide. Particles collected by impactors had diameters up to 20 μm diameter, with size and age dependent composition. Ash mass concentrations were derived from optical particle spectrometers for a particle density of 2.6 g cm−3 and various values of the refractive index (RI, real part: 1.59; 3 values for the imaginary part: 0, 0.004 and 0.008). The mass concentrations, effective diameters and related optical properties were compared with ground-based lidar observations. Theoretical considerations of particle sedimentation constrain the particle diameters to those obtained for the lower RI values. The ash mass concentration results have an uncertainty of a factor of two. The maximum ash mass concentration encountered during the 17 flights with 34 ash plume penetrations was below 1 mg m−3. The Falcon flew in ash clouds up to about 0.8 mg m−3 for a few minutes and in an ash cloud with approximately 0.2 mg m−3 mean-concentration for about one hour without engine damage. The ash plumes were rather dry and correlated with considerable CO and SO2 increases and O3 decreases. To first order, ash concentration and SO2 mixing ratio in the plumes decreased by a factor of two within less than a day. In fresh plumes, the SO2 and CO concentration increases were correlated with the ash mass concentration. The ash plumes were often visible slantwise as faint dark layers, even for concentrations below 0.1 mg m−3. The large abundance of volatile Aitken mode particles suggests previous nucleation of sulfuric acid droplets. The effective diameters range between 0.2 and 3 μm with considerable surface and volume contributions from the Aitken and coarse mode aerosol, respectively. The distal ash mass flux on 2 May was of the order of 500 (240–1600) kg s−1. The volcano induced about 10 (2.5–50) Tg of distal ash mass and about 3 (0.6–23) Tg of SO2 during the whole eruption period. The results of the Falcon flights were used to support the responsible agencies in their decisions concerning air traffic in the presence of volcanic ash.

Marked changes in human dispersal and development during the Middle to Upper Paleolithic transition have been attributed to massive volcanic eruption and/or severe climatic deterioration. We test this concept using records of volcanic ash layers of the Campanian Ignimbrite eruption dated to ca. 40,000 y ago (40 ka B.P.). The distribution of the Campanian Ignimbrite has been enhanced by the discovery of cryptotephra deposits (volcanic ash layers that are not visible to the naked eye) in archaeological cave sequences. They enable us to synchronize archaeological and paleoclimatic records through the period of transition from Neanderthal to the earliest anatomically modern human populations in Europe. Our results confirm that the combined effects of a major volcanic eruption and severe climatic cooling failed to have lasting impacts on Neanderthals or early modern humans in Europe. We infer that modern humans proved a greater competitive threat to indigenous populations than natural disasters.

Most of the global climate changes are closely associated with volcanic activity. However, the link between global cooling during the Ordovician‐Silurian (O‐S) transition and volcanism remains unclear due to limited constraints on large volcanic events before, during, and after the peak of the Hirnantian glaciation (PHG). Here, we present high‐resolution mercury (Hg) concentrations and isotopes from South China across the O‐S transition to assess volcanic activity and its contributions to climate changes. Anomalous Hg enrichments and volcanic‐range Hg isotopes in samples above volcanic ash layers confirm the effectiveness of Hg as a tracer of volcanic events. Variations in Hg isotopes across the O‐S transition reveal multiple Hg sources related to volcanic activity, that is, dominant volcanic Hg input during pre‐PHG and post‐PHG‐2, deposition of volcanic‐sourced atmospheric Hg(II) to seawater during PHG, and increased terrestrial Hg input from enhanced weathering during post‐PHG‐1. We propose that prolonged global cooling was driven by an albedo catastrophe caused by volcanic aerosols and sustained by reduced atmospheric CO2 levels due to enhanced organic carbon burial and weathering. This study highlights Hg as a tracer of volcanic activity and provides new evidence on the role of volcanism in driving climate changes across the O‐S transition.

During April–May 2010 the UK Facility for Airborne Atmospheric Measurements (FAAM) BAe‐146 aircraft flew 12 flights targeting volcanic ash clouds around the UK. The aircraft observed ash layers between altitudes of 2–8 km with peak mass concentrations typically between 200–2000μg/m3, as estimated from a Cloud and Aerosol Spectrometer (CAS). A peak value of 2000–5000 μg/m3 was observed over Scotland on 14 May 2010, although with considerable uncertainty due to the possible contamination by ice. Aerosol size distributions within ash clouds showed a fine mode (0.1–0.6 μm) associated with sulphuric acid and/or sulphate, and a coarse mode (0.6–35 μm) associated with ash. The ash mass was dominated by particles in the size range 1–10 μm (volume‐equivalent diameter), with a peak typically around 3–5μm. Electron‐microscope images and scattering patterns from the SID‐2H (Small Ice Detector) probe showed the highly irregular shape of the ash particles. Ash clouds were also accompanied by elevated levels of SO2 (10–100 ppbv), strong aerosol scattering (50–500 × 10−6 m−1), and low Ångstrom exponents (−0.5 to 0.4) from the 3‐wavelength nephelometer. Coarse‐mode mass specific aerosol extinction coefficients (kext), based on the CAS size distribution varied from 0.45–1.06 m2/g. A representative value of 0.6 m2/g is suggested for distal ash clouds (∼1000 km downwind) from this eruption. Key Points Assessing the risk of volcanic ash to aviation Validating ash forecasts from dispersion models Providing key physical/optical parameters for ash remote sensing

Uncertainty-bounded satellite retrievals of volcanic ash cloud properties such as ash cloud-top height, effective radius, optical depth and mass loading are needed for the robust quantitative assessment required to warn aviation of potential hazards. Moreover, there is an imperative to improve quantitative ash cloud estimation due to the planned move towards quantitative ash concentration forecasts by the Volcanic Ash Advisory Centers. Here we apply the Optimal Retrieval of Aerosol and Cloud (ORAC) algorithm to Advanced Himawari Imager (AHI) measurements of the ash clouds produced by the June 2019 Raikoke (Russia) eruption. The ORAC algorithm uses an optimal estimation technique to consolidate a priori information, satellite measurements and associated uncertainties into uncertainty-bounded estimates of the desired state variables. Using ORAC, we demonstrate several improvements in thermal infrared volcanic ash retrievals applied to broadband imagers. These include an improved treatment of measurement noise, accounting for multi-layer cloud scenarios, distinguishing between heights in the troposphere and stratosphere, and the retrieval of a wider range of effective radii sizes than existing techniques by exploiting information from the 10.4 µm channel. Our results indicate that 0.73 ± 0.40 Tg of very fine ash (radius ≤ 15 µm) was injected into the atmosphere during the main eruptive period from 21 June 18:00 UTC to 22 June 10:00 UTC. The total mass of very fine ash decreased from 0.73 to 0.10 Tg over ∼ 48 h, with an e-folding time of 20 h. We estimate a distal fine ash mass fraction of 0.73 % ± 0.62 % based on the total mass of very fine ash retrieved and the ORAC-derived height–time series. Several distinct ash layers were revealed by the ORAC height retrievals. Generally, ash in the troposphere was composed of larger particles than ash present in the stratosphere. We also find that median ash cloud concentrations fall below peak ash concentration safety limits (< 4 mg m−3) 11–16 h after the eruption begins, if typical ash cloud geometric thicknesses are assumed. The ORAC height retrievals for the near-source plume showed good agreement with GOES-17 side-view height data (R=0.84; bias = −0.75 km); however, a larger negative bias was found when comparing ORAC height retrievals for distal ash clouds against Cloud-Aerosol Lidar with Orthogonal Polarisation (CALIOP) measurements (R=0.67; bias = −2.67 km). The dataset generated here provides uncertainties at the pixel level for all retrieved variables and could potentially be used for dispersion model validation or be implemented in data assimilation schemes. Future work should focus on improving ash detection, improving height estimation in the stratosphere and exploring the added benefit of visible channels for retrieving effective radius and optical depth in opaque regions of nascent ash plumes.

Ombrotrophic bogs in southern Patagonia have been examined with regard to paleoclimatic and geochemical research questions but knowledge about organic matter decomposition in these bogs is limited. Therefore, we examined peat humification with depth by Fourier Transformed Infrared (FTIR) measurements of solid peat, C/N ratio, and δ13C and δ15N isotope measurements in three bog sites. Peat decomposition generally increased with depth but distinct small scale variation occurred, reflecting fluctuations in factors controlling decomposition. C/N ratios varied mostly between 40 and 120 and were significantly correlated (R2 > 0.55, p < 0.01) with FTIR-derived humification indices. The degree of decomposition was lowest at a site presently dominated by Sphagnum mosses. The peat was most strongly decomposed at the driest site, where currently peat-forming vegetation produced less refractory organic material, possibly due to fertilizing effects of high sea spray deposition. Decomposition of peat was also advanced near ash layers, suggesting a stimulation of decomposition by ash deposition. Values of δ13C were 26.5 ± 2‰ in the peat and partly related to decomposition indices, while δ15N in the peat varied around zero and did not consistently relate to any decomposition index. Concentrations of DOM partly related to C/N ratios, partly to FTIR derived indices. They were not conclusively linked to the decomposition degree of the peat. DOM was enriched in 13C and in 15N relative to the solid phase probably due to multiple microbial modifications and recycling of N in these N-poor environments. In summary, the depth profiles of C/N ratios, δ13C values, and FTIR spectra seemed to reflect changes in environmental conditions affecting decomposition, such as bog wetness, but were dominated by site specific factors, and are further influenced by ash deposition and possibly by sea spray input.