Geology Reports⌕ Search

Geology topics

T. Sisson

Publications and source records attributed to T. Sisson.

4 recordsLinked to original sources

Evolution of melt-vapor surface tension in silicic volcanic systems: Experiments with hydrous melts

We evaluate the melt‐vapor surface tension (σ) of natural, water‐saturated dacite melt at 200 MPa, 950–1055°C, and 4.8–5.7 wt % H 2 O. We experimentally determine the critical supersaturation pressure for bubble nucleation as a function of dissolved water and then solve for σ at those conditions using classical nucleation theory. The solutions obtained give dacite melt‐vapor surface tensions that vary inversely with dissolved water from 0.042 (±0.003) J m −2 at 5.7 wt % H 2 O to 0.060 (±0.007) J m −2 at 5.2 wt % H 2 O to 0.073 (±0.003) J m −2 at 4.8 wt % H 2 O. Combining our dacite results with data from published hydrous haplogranite and high‐silica rhyolite experiments reveals that melt‐vapor surface tension also varies inversely with the concentration of mafic melt components (e.g., CaO, FeO total , MgO). We develop a thermodynamic context for these observations in which melt‐vapor surface tension is represented by a balance of work terms controlled by melt structure. Overall, our results suggest that cooling, crystallization, and vapor exsolution cause systematic changes in σ that should be considered in dynamic modeling of magmatic processes.

Journal of Geophysical Research B: Solid Earth↗

Gas evolution in eruptive conduits: Combining insights from high temperature and pressure decompression experiments with steady-state flow modeling

In this paper we examine the consequences of bubble nucleation mechanism on eruptive degassing of rhyolite magma. We use the results of published high temperature and pressure decompression experiments as input to a modified version of CONFLOW, the numerical model of Mastin and Ghiorso [(2000) U.S.G.S. Open-File Rep. 00-209, 53 pp.] and Mastin [(2002) Geochem. Geophys. Geosyst. 3, 10.1029/2001GC000192] for steady, two-phase flow in vertical conduits. Synthesis of the available experimental data shows that heterogeneous nucleation is triggered at ΔP <5–20 MPa in water-saturated rhyolite and leads to equilibrium degassing through a discrete nucleation event. Typically 10 5 –10 7 bubbles/cm 3 are produced which evolve Gaussian bubble size distributions. Homogeneous nucleation requires ΔP >120–150 MPa, and leads to disequilibrium degassing at extreme H 2 O supersaturation. In this latter case, nucleation is an ongoing process controlled by changing supersaturation conditions. Exponential bubble size distributions are often produced with number densities of 10 6 –10 9 bubbles/cm 3 . Our numerical analysis adopts an end-member approach that specifically compares equilibrium degassing with delayed, disequilibrium degassing characteristic of homogeneously-nucleating systems. The disequilibrium simulations show that delaying nucleation until ΔP =150 MPa restricts degassing to within ∼1500 m of the surface. Fragmentation occurs at similar porosity in both the disequilibrium and equilibrium modes (∼80 vol%), but at the distinct depths of ∼500 m and ∼2300 m, respectively. The vesiculation delay leads to higher pressures at equivalent depths in the conduit, and the mass flux and exit pressure are each higher by a factor of ∼2.0. Residual water contents in the melt reaching the vent are between 0.5 and 1.0 wt%, roughly twice that of the equilibrium model.

Journal of Volcanology and Geothermal Research↗

Delayed, disequilibrium degassing in rhyolite magma: Decompression experiments and implications for explosive volcanism

Recent numerical models and analog shock tube experiments show that disequilibrium degassing during magma ascent may lead to violent vesiculation very near the surface. In this study a series of decompression experiments using crystal-free, rhyolite melt were conducted to examine the development of large supersaturations due to delayed, homogenous (spontaneous) bubble nucleation. Melts were saturated at 900??C and 200 MPa with either 5.2 wt% dissolved H2O, or with 4.2 wt% H2O and 640 ppm CO2, and isothermally decompressed at linear rates of either 0.003, 0.025, or 8.5 MPa/s to final pressures between 25 and 175 MPa. Additional isobaric saturation experiments (900??C, 200-25 MPa) using pure H2O or mixed H2O-CO2 fluids establish reference equilibrium solubility curves/values. Homogenous nucleation is triggered in both H2O-only and H2O-CO2 experiments once the supersaturation pressure (??Pss) reaches ?? 120-150 MPa and the melt contains ?? two times its equilibrium water contents. Bubble number density and nucleation rate depend on the supersaturation pressure, with values on the order of 102/cm3 and < 1/cm3/s for ??Pss~120 MPa; 106/cm3 and 103-105/cm3/s for ??Pss??~130-150 MPa; and 107/cm3 and 106/cm3/s for ??Pss??160-175 MPa. Nucleation rates are consistent with classical nucleation theory, and infer an activation energy for nucleation of 1.5 x 10-18 J/nucleus, a critical bubble radius of 2 x 10-9 m, and an effective surface tension for rhyolite at 5.2 wt% H2O and 900??C of 0.10-0.11 N/m. The long nucleation delay limits the time available for subsequent diffusion such that disequilibrium dissolved H2O and CO2 contents persist to the end of our runs. The disequilibrium degassing paths inferred from our experiments contrast markedly with the equilibrium or quasi-equilibrium paths found in other studies where bubble nucleation occurs heterogenously on crystals or other discontinuities in the melt at low ??Pss. Homogenous and heterogenous nucleation rates are comparable, however, as are bubble number densities, so that at a given decompression rate it appears that nucleation mechanism, rather than nucleation rate, determines degassing efficiency by fixing the pressure (depth) at which vesiculation commences and hence the time available for equilibration prior to eruption. Although real systems are probably never truly crystal-free, our results show that rhyolitic magmas containing up to 104 crystals/cm3, and perhaps as high as 106 crystals/cm3, are controlled by homogenous, rather than heterogenous, nucleation during ascent. ?? 2000 Elsevier Science B.V. All rights reserved.

Earth and Planetary Science Letters↗