Geology topics

W.I. Rose

Publications and source records attributed to W.I. Rose.

5 recordsLinked to original sources

USGS2012

Water-soluble material on aerosols collected within volcanic eruption clouds

In February and March of 1978, filter samplers mounted on an aircraft were used to collect the aerosol fraction of the eruption clouds from three active Guatemalan volcanoes (Fuego, Pacaya, and Santiaguito). The samples were collected on Teflon (Fluoropore) filters with a nominal pore diameter of 0.5μm. The mass of air sampled by the filters ranged from 0.15 to 6.6 kg. The particulate material collected consisted of fragments of angular silicate ash and droplets of what is interpreted as dilute H 2 SO 4 and HCl. After collection of the samples, each filter was rinsed with 60 ml of distilled-deionized water. Splits of each extract were centrifuged to remove particles greater than or equal to 0.1 μm in diameter, acidified, and analyzed for B, Ba, Be, Ca, Cd, Co, Cu, Fe, Li, Mg, Mn, Mo, Na, Pb, Si, Sr, V, and Zn by inductively coupled plasma—optical emission spectroscopy. Separate splits were analyzed for F and Cl by specific-ion-electrode methods and for U by a fission track technique. The elements dissolved in the aqueous extracts represent components of water-soluble material either formed directly in the eruption cloud or derived from interaction of ash particles and aerosol components of the plume. Calculations of enrichment factors, based upon concentration ratios, showed the elements most enriched in the extracts relative to bulk ash composition were Cd, Cu, V, F, Cl, Zn, and Pb. These elements represent a subset (with the addition of Cl and F) of elements previously reported enriched in atmospheric aerosols in remote regions as well as in volcanic areas. This suggests that some of the enriched elements were widely dispersed as volatile halides emitted from a volcanic source.

Journal of Geophysical Research - Oceans↗

USGS2009

A multidisciplinary effort to assign realistic source parameters to models of volcanic ash-cloud transport and dispersion during eruptions

During volcanic eruptions, volcanic ash transport and dispersion models (VATDs) are used to forecast the location and movement of ash clouds over hours to days in order to define hazards to aircraft and to communities downwind. Those models use input parameters, called “eruption source parameters”, such as plume height H , mass eruption rate Ṁ , duration D , and the mass fraction m 63 of erupted debris finer than about 4ϕ or 63 μm, which can remain in the cloud for many hours or days. Observational constraints on the value of such parameters are frequently unavailable in the first minutes or hours after an eruption is detected. Moreover, observed plume height may change during an eruption, requiring rapid assignment of new parameters. This paper reports on a group effort to improve the accuracy of source parameters used by VATDs in the early hours of an eruption. We do so by first compiling a list of eruptions for which these parameters are well constrained, and then using these data to review and update previously studied parameter relationships. We find that the existing scatter in plots of H versus Ṁ yields an uncertainty within the 50% confidence interval of plus or minus a factor of four in eruption rate for a given plume height. This scatter is not clearly attributable to biases in measurement techniques or to well-recognized processes such as elutriation from pyroclastic flows. Sparse data on total grain-size distribution suggest that the mass fraction of fine debris m 63 could vary by nearly two orders of magnitude between small basaltic eruptions (∼ 0.01) and large silicic ones (> 0.5). We classify eleven eruption types; four types each for different sizes of silicic and mafic eruptions; submarine eruptions; “brief” or Vulcanian eruptions; and eruptions that generate co-ignimbrite or co-pyroclastic flow plumes. For each eruption type we assign source parameters. We then assign a characteristic eruption type to each of the world's ∼ 1500 Holocene volcanoes. These eruption types and associated parameters can be used for ash-cloud modeling in the event of an eruption, when no observational constraints on these parameters are available.

Journal of Volcanology and Geothermal Research↗

USGS1982

Leachability of uranium and other elements from freshly erupted volcanic ash

A study of leaching of freshly erupted basaltic and dacitic air-fall ash and bomb fragment samples, unaffected by rain, shows that glass dissolution is the dominant process by which uranium is initially mobilized from air-fall volcanic ash. Si, Li, and V are also preferentially mobilized by glass dissolution. Gaseous transfer followed by fixation of soluble uranium species on volcanic-ash particles is not an important process affecting uranium mobility. Gaseous transfer, however, may be important in forming water-soluble phases, adsorbed to ash surfaces, enriched in the economically and environmentally important elements Zn, Cu, Cd, Pb, B, F, and Ba. Quick removal of these adsorbed elements by the first exposure of freshly erupted ash to rain and surface water may pose short-term hazards to certain forms of aquatic and terrestrial life. Such rapid release of material may also represent the first step in transportation of economically important elements to environments favorable for precipitation into deposits of commercial interest. Ash samples collected from the active Guatemalan volcanoes Fuego and Pacaya (high-Al basalts) and Santiaguito (hornblende-hypersthene dacite); bomb fragments from Augustine volcano (andesite-dacite), Alaska, and Heimaey (basalt), Vestmann Islands, Iceland; and fragments of "rhyolitic" pumice from various historic eruptions were subjected to three successive leaches with a constant water-to-ash weight ratio of 4:1. The volcanic material was successively leached by: (1) distilled-deionized water (pH = 5.0-5.5) at room temperature for 24 h, which removes water-soluble gases and salts adsorbed on ash surfaces during eruption; (2) dilute HCl solution (pH = 3.5-4.0) at room temperature for 24 h, which continues the attack initiated by the water and also attacks acid-soluble sulfides and oxides; (3) a solution 0.05 M in both Na,CO, and NaHCO, (pH = 9.9) at 80°C for one week, which preferentially dissolves volcanic glass. The first two leaches mimic interaction of ash with rain produced in the vicinity of an active eruption. The third leach accelerates the effect of prolonged contact of volcanic ash with alkaline ground water present during ash diagenesis.

Journal of Volcanology and Geothermal Research↗

USGS1980

Uranium contents of glassy and devitrified andesites and dacites, Mount Mazama, Oregon

By direct comparison of devitrified and granophyrically crystallized specimens with nonhydrated glassy materials from the same units, Rosholt and coworkers (Rosholt and Noble, 1969; Rosholt et al., 1971) showed that specimens of primarily crystallized but otherwise unaltered peralkaline and subalkaline rhyolite from the western United States had lost from 30 to 80 percent of the uranium that they originally possessed. They suggested that uranium was lost both during crystallization, perhaps as the volatile hexafluoride, and/or later through the action of ground water. Similar results have been obtained by Shatkov et al. (1970) and Kovalev and Maylasova (1973). Zielinski (1978) compared the uranium contents of paired nonhydrated glassy and primarily devitrified phases of a number of subalkaline rhyolitic lavas and tuffs from various localities in the western United States. He found a generally smaller degree of uranium loss than had been observed by Rosholt et al. (1971) for peralkaline materials. In addition, Zielinski noted that older specimens had, as a group, lost a greater percentage of their original uranium than had younger rocks and suggested that uranium is generally lost progressively over periods of many millions of years.

Oregon↗

USGS1980

Oxygen isotopic determinations of sequentially erupted plagioclases in the 1974 magma of Fuego Volcano, Guatemala

Plagioclases in the 1974 high-Al basalt from Fuego Volcano have ??O18 values of +6.0 to +8.5 per mil. Meteoric water cannot have played a significant role in Fuego's magma. Large, weakly zone clear phenocrysts had ??O18 values in the accepted mantle range, while patchyzoned and oscillatory-zoned plagioclases inferred to have formed later and shallower levels have slightly heavier oxygen isotopic ratios. ?? 1980 Intern. Association of Volcanology and Chemistry of the Earth's Interior.

Bulletin Volcanologique↗