Modified HNO3 seasonality in volcanic layers of a polar ice core: Snow-pack effect or photochemical perturbation?

Using the chemical composition of snow and ice of a central Greenland ice core, we have investigated changes in atmospheric HNO₃ chemistry following the large volcanic eruptions of Laki (1783), Tambora (1815) and Katmai (1912). The concentration of several cations and anions, including SO ₄ ^2– and NO ₃ ^– , were measured using ion chromatography. We found that following those eruptions, the ratio of the concentration of NO ₃ ^– deposited during winter to that deposited during summer was significantly higher than during nonvolcanic periods. Although we cannot rule out that this pattern originates from snow pack effects, we propose that increased concentrations of volcanic H₂SO₄ particles in the stratosphere may have favored condensation and removal of HNO₃ from the stratosphere during Arctic winter. In addition, this pattern might have been enhanced by slower formation of HNO₃ during summer, caused by direct consumption of OH through oxidation of volcanic SO₂.     

Magmatic and phreatomagmatic volcanic activity at Mt. Takahe, West Antarctica, based on tephra layers in the Byrd ice core and field observations at Mt. Takahe

The morphology, grain size characteristics and composition of ash particles in 30 ka to 150 ka tephra layers from the Byrd ice core were examined to characterize the eruptions which produced them and to test the suggestion that they were erupted from Mt. Takahe, a shield volcano in Marie Byrd Land, West Antarctica. Volcanic deposits at Mt. Takahe were examined for evidence of recent activity which could correlate with the tephra layers in the ice core.Coarse- and fine-ash layers have been recognized in the Byrd ice core. The coarse-ash layers have a higher mass concentration than the fine-ash layers and are characterized by fresh glass shards > 50 μm diameter, many containing elongate pipe vesicles. The fine-ash layers have a lower mass concentration and contain a greater variety of particles, typically < 20 μm diameter. Many of these particles are aggregate grains composed of glass and crystal fragments showing S and Cl surface alteration. The grain-size distributions of the coarse and fine-ash layers overlap, in part because of the aggregate nature of grains in the fine-ash layers. The coarse-ash layers are interpreted as having formed by magmatic eruption whereas the fine-ash layers are believed to be hydrovolcanic in origin.Mt. Takahe is the favored source for the tephra because: (a) chemical analyses of samples from the volcano are distinctive, being peralkaline trachyte, and similar in composition to the analyzed tephra; (b) Mt. Takahe is a young volcano (< 0.3 Ma); (c) pyroclastic deposits on Mt. Takahe indicate styles of eruption similar to that inferred for the ice core tephra; and (d) Mt. Takahe is only about 350 km from the calculated site of tephra deposition.A speculative eruptive history for Mt. Takahe is established by combining observations from Mt. Takahe and the Byrd ice core tephra. Initial eruptions at Mt. Takahe were subglacial and then graded into alternating subaerial and subglacial activity. The tephra suggest alternating subaerial magmatic and hydrovolcanic eruptions from 30 to 20 ka B.P., followed by a sustained period of hydrovolcanic eruptions from 20 to 14 ka B.P., which peaked at 18 ka B.P.     

Characteristics and Possible Source of a 1479 A.D. Volcanic Ash Layer in a Greenland Ice Core

A microparticle concentration peak in a GISP2 ice core contains volcanic glass shards of rhyolitic composition that correspond in age to the 1479-1480 A.D. Mt. St. Helens Wn eruption. These glass shards are compositionally similar to the Wn tephra and constitute 83% of the total particle population. The shards are very coarse-grained (up to 40 μm diameter), suggesting rapid transport from their source to Greenland. A major sulfate peak in the ice occurs approximately 4 months after deposition of the glass shards. This difference in depositional timing suggests primarily tropospheric transport of the ash and stratospheric transport of the sulfate aerosol. Large-scale climatic perturbations following this eruption were evidently negligible. Glaciochemical seasonal indicators suggest a late-fall to early-winter 1479 A.D. eruption.     

Fluxes,sizes, morphology and compositions of particles in the Mt. Erebus volcanic plume,December 1983

Use of an airborne quartz crystal microbalance cascade impactor instrument together with a correlation spectrometer has allowed the flux of particles and their size distribution to be determined at Mount Erebus. The plume contributes 21±3 metric tomnes/day of aerosol particles to the Antarctic upper troposphere. The aerosol particles consist of larger (5–25 m) particles of elemental sulfur and silica, a middle sized group of iron oxides and smaller particles (less than 1 m) of complex liquids. Unlike many volcanic plumes, the Erebus plume has only a small amount of sulfate particles. The concentrations of particles in the Erebus plumes was 70–370 m/m³. Limited sampling of the Antarctic atmosphere at 8 km altitude but hundreds of km away from Erebus obtained a few large particles of sulfur and silicates, suggesting a similarity with the Erebus plume. The fallout of these particles occurs slowly over a broad area of the Antarctic continent.