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- All Subjects: Analytical Chemistry
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- All Subjects: Nitrogen Cycle
- All Subjects: Obsidian--Spectra.
- All Subjects: Petrology
- Genre: Academic theses
- Creators: Roggensack, Kurt
Description
Volcanic devolatilization is one of the major processes in the global nitrogen cycle. Past studies have often estimated the magnitude of this flux using volcanic emission measurements, which are limited to currently active systems and sensitive to atmospheric contamination. A different methodological approach requires appropriate analytical parameters for nitrogen analysis in silicate glasses by secondary ion mass spectrometry (SIMS), which have not yet been established. To this end, we analyze various ion implanted basaltic and rhyolitic glasses by SIMS. We demonstrate that water content significantly affects the ion yields of 14N+ and 14N16O−, as well as the background intensity of 14N+ and 12C+. Application of implant-derived calibrations to natural samples provide the first reported concentrations of nitrogen in melt inclusions. These measurements are from samples from the Bishop Tuff in California, the Huckleberry Ridge Tuff of the Yellowstone Volcanic Center, and material from the Okaia and Oruanui eruptions in the Taupo Volcanic Center. In all studied material, we find maximum nitrogen contents of less than 45 ppm and that nitrogen concentration varies positively with CO2 concentration, which is interpreted to reflect partial degassing trend. Using the maximum measured nitrogen contents for each eruption, we find that the Bishop released >3.6 x 1013 g of nitrogen, the Huckleberry Ridge released >1.3 x 1014 g, the Okaia released >1.1 x 1011 g of nitrogen, the Oruanui released >4.7 x 1013 g of nitrogen. Simple calculations suggest that with concentrations such as these, rhyolitic eruptions may ephemerally increase the nitrogen flux to the atmosphere, but are insignificant compared to the 4 x 1021 g of nitrogen stored in the atmosphere.
ContributorsRegier, Margo Elaine (Author) / Hervig, Richard L (Thesis advisor) / Roggensack, Kurt (Committee member) / Till, Christy B. (Committee member) / Arizona State University (Publisher)
Created2016
Description
Volcanoes can experience multiple eruption styles throughout their eruptive histories. Among the most complex and most common are eruptions of intermediate explosivity, such as Vulcanian and sub-Plinian eruptions. Vulcanian eruptions are characterized by small-scale, short-lived, ash-rich eruptions initiated by the failure of a dense magma plug or overlying dome that had sealed an overpressured conduit. Sub-Plinian eruptions are characterized by sustained columns that reach tens of kilometers in height.
Multiple eruption styles can be observed in a single eruptive sequence. In recent decades, transitions in eruption style during well-documented eruptions have been described in detail, with some workers proposing explanatory mechanisms for the transitions. These proposed mechanisms may be broadly classified into processes at depth, processes in the conduit, or some combination of both.
The present study is focused on the Pietre Cotte sequence because it may have encompassed up to three different eruptive cycles, each representing different degrees of explosivity. The first deposits are composed of repeated layers of fine ash and lapilli composed of latite and rhyolite endmembers, efficiently mixed at sub-cm scales. The thin layers and bubble/crystal textures indicate that the magma underwent numerous decompressions and open-system degassing, and that the eruptions waned with time. The second phase of the sequence appears to have been initiated by cm-scale mixing between a volatile-rich, mafic magma from deeper in the system and a shallow silicic body. Textures indicate that the magma ascended rapidly and experienced little to no open-system degassing. The final phase of the sequence again produced repeated layers of fine ash and lapilli, of uniform trachyte composition, and waned with time. The first and last phases were likely produced in Vulcanian eruptions, while the pumice-rich layers were likely produced in Vulcanian to sub-Plinian eruptions.
In summary, the Pietre Cotte sequence is characterized by up to three magma recharge events in ~200 years. The differences in eruptive style appear to have been controlled by variations in the volatile content of the recharge magma, as well as the efficiency and scale of magma mixing and resulting overpressures.
Multiple eruption styles can be observed in a single eruptive sequence. In recent decades, transitions in eruption style during well-documented eruptions have been described in detail, with some workers proposing explanatory mechanisms for the transitions. These proposed mechanisms may be broadly classified into processes at depth, processes in the conduit, or some combination of both.
The present study is focused on the Pietre Cotte sequence because it may have encompassed up to three different eruptive cycles, each representing different degrees of explosivity. The first deposits are composed of repeated layers of fine ash and lapilli composed of latite and rhyolite endmembers, efficiently mixed at sub-cm scales. The thin layers and bubble/crystal textures indicate that the magma underwent numerous decompressions and open-system degassing, and that the eruptions waned with time. The second phase of the sequence appears to have been initiated by cm-scale mixing between a volatile-rich, mafic magma from deeper in the system and a shallow silicic body. Textures indicate that the magma ascended rapidly and experienced little to no open-system degassing. The final phase of the sequence again produced repeated layers of fine ash and lapilli, of uniform trachyte composition, and waned with time. The first and last phases were likely produced in Vulcanian eruptions, while the pumice-rich layers were likely produced in Vulcanian to sub-Plinian eruptions.
In summary, the Pietre Cotte sequence is characterized by up to three magma recharge events in ~200 years. The differences in eruptive style appear to have been controlled by variations in the volatile content of the recharge magma, as well as the efficiency and scale of magma mixing and resulting overpressures.
ContributorsKim, Jisoo (Author) / Clarke, Amanda B (Thesis advisor) / Roggensack, Kurt (Thesis advisor) / Barboni, Melanie (Committee member) / Arizona State University (Publisher)
Created2020
Description
A novel technique for measuring heavy trace elements in geologic materials with secondary ion mass spectrometry (SIMS) is presented. This technique combines moderate levels of mass resolving power (MRP) with energy filtering in order to remove molecular ion interferences while maintaining enough sensitivity to measure trace elements. The technique was evaluated by measuring a set of heavy chalcophilic elements in two sets of doped glasses similar in composition to rhyolites and basalts, respectively. The normalized count rates of Cu, As, Se, Br, and Te were plotted against concentrations to test that the signal increased linearly with concentration. The signal from any residual molecular ion interferences (e.g. ²⁹Si³⁰Si¹⁶O on ⁷⁵As) represented apparent concentrations ≤ 1 μg/g for most of the chalcophiles in rhyolitic matrices and between 1 and 10 μg/g in basaltic compositions. This technique was then applied to two suites of melt inclusions from the Bandelier Tuff: Ti-rich, primitive and Ti-poor, evolved rhyolitic compositions. The results showed that Ti-rich inclusions contained ~30 μg/g Cu and ~3 μg/g As while the Ti-poor inclusions contained near background Cu and ~6 μg/g As. Additionally, two of the Ti-rich inclusions contained > 5 μg/g of Sb and Te, well above background. Other elements were at or near background. This suggests certain chalcophilic elements may be helpful in unraveling processes relating to diversity of magma sources in large eruptions. Additionally, an unrelated experiment is presented demonstrating changes in the matrix effect on SIMS counts when normalizing against ³⁰Si⁺ versus ²⁸Si²⁺. If one uses doubly charged silicon as a reference, (common when using large-geometry SIMS instruments to study the light elements Li - C) it is important that the standards closely match the major element chemistry of the unknown.
ContributorsCarlson, Eric Norton (Author) / Hervig, Richard L (Thesis advisor) / Roggensack, Kurt (Committee member) / Burt, Donald M (Committee member) / Arizona State University (Publisher)
Created2021