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A.J. Sutton

Publications and source records attributed to A.J. Sutton.

4 recordsLinked to original sources

Kilauea's 5-9 March 2011 Kamoamoa fissure eruption and its relation to 30+ years of activity from Pu'u 'Ō'ō

Lava output from Kīlauea's long-lived East Rift Zone eruption, ongoing since 1983, began waning in 2010 and was coupled with uplift, increased seismicity, and rising lava levels at the volcano's summit and Pu‘u ‘Ō‘ō vent. These changes culminated in the four-day-long Kamoamoa fissure eruption on the East Rift Zone starting on 5 March 2011. About 2.7 × 10 6 m 3 of lava erupted, accompanied by ˜15 cm of summit subsidence, draining of Kīlauea's summit lava lake, a 113 m drop of Pu‘u ‘Ō‘ō's crater floor, ˜3 m of East Rift Zone widening, and eruptive SO 2 emissions averaging 8500 tonnes/day. Lava effusion resumed at Pu‘u ‘Ō‘ō shortly after the Kamoamoa eruption ended, marking the onset of a new period of East Rift Zone activity. Multiparameter monitoring before and during the Kamoamoa eruption suggests that it was driven by an imbalance between magma supplied to and erupted from Kīlauea's East Rift Zone and that eruptive output is affected by changes in the geometry of the rift zone plumbing system. These results imply that intrusions and eruptive changes during ongoing activity at Kīlauea may be anticipated from the geophysical, geological, and geochemical manifestations of magma supply and magma plumbing system geometry.

Hawaii

Groundwater chemistry in the vicinity of the Puna Geothermal Venture Power Plant, Hawai‘i, after two decades of production

We report chemical data for selected shallow wells and coastal springs that were sampled in 2014 to determine whether geothermal power production in the Puna area over the past two decades has affected the characteristics of regional groundwater. The samples were analyzed for major and minor chemical species, trace metals of environmental concern, stable isotopes of water, and two organic compounds (pentane and isopropanol) that are injected into the deep geothermal reservoir at the power plant. Isopropanol was not detected in any of the groundwaters; confirmed detection of pentane was restricted to one monitoring well near the power plant at a low concentration not indicative of source. Thus, neither organic compound linked geothermal operations to groundwater contamination, though chemical stability and transport velocity questions exist for both tracers. Based on our chemical analysis of geothermal fluid at the power plant and on many similar results from commercially analyzed samples, we could not show that geothermal constituents in the groundwaters we sampled came from the commercially developed reservoir. Our data are consistent with a long-held view that heat moves by conduction from the geothermal reservoir into shallow groundwaters through a zone of low permeability rock that blocks passage of geothermal water. The data do not rule out all impacts of geothermal production on groundwater. Removal of heat during production, for example, may be responsible for minor changes that have occurred in some groundwater over time, such as the decline in temperature of one monitoring well near the power plant. Such indirect impacts are much harder to assess, but point out the need for an ongoing groundwater monitoring program that should include the coastal springs down-gradient from the power plant.

Hawaii

The first five years of Kīlauea’s summit eruption in Halema‘uma‘u Crater, 2008–2013

The eruption in Halema‘uma‘u Crater that began in March 2008 is the longest summit eruption of Kīlauea Volcano, on the Island of Hawai‘i, since 1924. From the time the eruption began, the new "Overlook crater" inside Halema‘uma‘u has exhibited fluctuating lava lake activity, occasional small explosive events, and a persistent gas plume. The beautiful nighttime glow impresses and thrills visitors in Hawai‘i Volcanoes National Park, but the continuous emission of sulfur dioxide gas produces "vog" (volcanic smog) that can severely affect communities and local agriculture downwind. U.S. Geological Survey scientists continue to closely monitor the eruption and assess ongoing hazards.

Hawai'i

Enhancement of the volcanogenic "bromine explosion" via reactive nitrogen chemistry (Kīlauea volcano, Hawai'i)

Since the first detection of bromine monoxide in volcanic plumes attention has focused on the atmospheric synthesis and impact of volcanogenic reactive halogens. We report here new measurements of BrO in the volcanic plume emitted from Kīlauea volcano – the first time reactive halogens have been observed in emissions from a hotspot volcano. Observations were carried out by ground-based Differential Optical Absorption Spectroscopy in 2007 and 2008 at Pu'u' O ' o crater, and at the 2008 magmatic vent that opened within Halema'uma'u crater. BrO was readily detected in the Halema'uma'u plume (average column amount of 3×1015 molec cm −2 ) and its abundance was strongly correlated with that of SO 2 . However, anticorrelation between NO 2 and SO 2 (and BrO) abundances in the same plume strongly suggest an active role of NO x in reactive halogen chemistry. The calculated SO 2 /BrO molar ratio of ~1600 is comparable to observations at other volcanoes, although the BrO mixing ratio is roughly double that observed elsewhere. While BrO was not observed in the Pu'u' O ' o plume this was probably merely a result of the detection limit of our measurements and based on understanding of the Summit and East Rift magmatic system we expect reactive halogens to be formed also in the Pu'u' O ' o emissions. If this is correct then based on the long term SO 2 flux from Pu'u' O ' o we calculate that Kīlauea emits ~480 Mg yr −1 of reactive bromine and may thus represent an important source to the tropical Pacific troposphere.

Hawaii