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Acoustic compressional and shear wave velocities (VP, VS) of anhydrous (AHRG) and hydrous rhyolitic glasses (HRG) containing 3.28 wt% (HRG-3) and 5.90 wt% (HRG-6) total water concentra- tion (H2Ot) have been measured using Brillouin light scattering (BLS) spectroscopy up to 3 GPa in a diamond-anvil cell at ambient temperature. In addition, Fourier-transform infrared (FTIR) spectroscopy was used to measure the speciation of H2O in the glasses up to 3 GPa. At ambient pressure, HRG-3 contains 1.58 (6) wt% hydroxyl groups (OH–) and 1.70 (7) wt% molecular water (H2Om) while HRG-6 contains 1.67 (10) wt% OH– and 4.23 (17) wt% H2Om where the numbers in parentheses are ±1σ. With increasing pressure, very little H2Om, if any, converts to OH– within uncertainties in hydrous rhyolitic glasses such that HRG-6 contains much more H2Om than HRG-3 at all experimental pressures. We observe a nonlinear relationship between high-pressure sound velocities and H2Ot, which is attributed to the distinct effects of each water species on acoustic velocities and elastic moduli of hydrous glasses. Near ambient pressure, depolymerization due to OH– reduces VS and G more than VP and KS. VP and KS in both anhydrous and hydrous glasses decrease with increasing pressure up to ~1–2 GPa before increasing with pressure. Above ~1–2 GPa, VP and KS in both hydrous glasses converge with those in AHRG. In particular, VP in HRG-6 crosses over and becomes higher than VP in AHRG. HRG-6 displays lower VS and G than HRG-3 near ambient pressure, but VS and G in these glasses converge above ~2 GPa. Our results show that hydrous rhyolitic glasses with ~2–4 wt% H2Om can be as incompressible as their anhydrous counterpart above ~1.5 GPa. The nonlinear effects of hydration on high-pressure acoustic velocities and elastic moduli of rhyolitic glasses observed here may provide some insight into the behavior of hydrous silicate melts in felsic magma chambers at depth. 

Following rapid decompression in the conduit of a volcano, magma breaks into ash- to block-sized fragments, powering explosive sub-Plinian and Plinian eruptions that may generate destructive pyroclastic falls and flows. It is thus crucial to assess how magma breaks up into fragments. This task is difficult, however, because of the subterranean nature of the entire process and because the original size of pristine fragments is modified by secondary fragmentation and expansion. New textural observations of sub-Plinian and Plinian pumice lapilli reveal that some primary products of magma fragmentation survive by sintering together within seconds of magma break-up. Their size distributions reflect the energetics of fragmentation, consistent with products of rapid decompression experiments. Pumice aggregates thus offer a unique window into the previously inaccessible primary fragmentation process and could be used to determine the potential energy of fragmentation. 

Silicic volcanic activity has long been framed as either violently explosive or gently effusive. However, recent ob- servations demonstrate that explosive and effusive behavior can occur simultaneously. Here, we propose that rhyolitic magma feeding subaerial eruptions generally fragments during ascent through the upper crust and that effusive eruptions result from conduit blockage and sintering of the pyroclastic products of deeper cryptic frag- mentation. Our proposal is supported by (i) rhyolitic lavas are volatile depleted; (ii) textural evidence supports a pyroclastic origin for effusive products; (iii) numerical models show that small ash particles !10−5 m can diffusive- ly degas, stick, and sinter to low porosity, in the time available between fragmentation and the surface; and (iv) inferred ascent rates from both explosive and apparently effusive eruptions can overlap. Our model reconciles previously paradoxical observations and offers a new framework in which to evaluate physical, numerical, and geochemical models of Earth’s most violent volcanic eruptions.