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A. J. Sutton

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

14 recordsLinked to original sources
USGS2018

Measuring SO2 emission rates at Kīlauea Volcano, Hawaii, using an array of upward-looking UV spectrometers, 2014-2017

Retrieving accurate volcanic sulfur dioxide (SO 2 ) gas emission rates is important for a variety of purposes. It is an indicator of shallow subsurface magma, and thus may signal impending eruption or unrest. SO 2 emission rates are significant for accurately assessing climate impact, and providing context for assessing environmental, agricultural, and human health effects during volcanic eruptions. The U.S. Geological Survey Hawaiian Volcano Observatory uses an array of ten fixed, upward-looking ultraviolet spectrometer systems to measure SO 2 emission rates at 10-s sample intervals from the Kīlauea summit. We present Kīlauea SO 2 emission rates from the volcano’s summit and middle East Rift Zone during 2014–2017 and discuss the major sources of error for these measurements. Due to the wide range of SO 2 emissions encountered at the summit vent, we used a variable wavelength spectral analysis range to accurately quantify both high and low SO 2 column densities. We compare measured emission rates from the fixed spectrometer array to independent road and helicopter-based traverse measurements and evaluate the magnitudes and sources of uncertainties for each method. To address the challenge of obtaining accurate plume speed measurements, we examine ground-based wind-speed, plume speed tracking via spectrometer, and SO 2 camera derived plume speeds. Our analysis shows that: (1) the summit array column densities calculated using a dual fit window, are within -6 to +22% of results obtained with a variety of other conventional and experimental retrieval methods; (2) emission rates calculated from the summit array located ∼3 km downwind provide the best, practical estimate of summit SO 2 release under normal trade wind conditions; (3) ground-based anemometer wind speeds are 22% less than plume speeds determined by cross-correlation of plume features; (4) our best estimate of average Kīlauea SO 2 release for 2014–2017 is 5100 t/d, which is comparable to the space-based OMI emissions of 5518 t/d; and (5) short-term variability of SO 2 emissions reflects Kīlauea lava lake dynamics.

Hawaii↗
USGS2012

Sulfur dioxide emission rates from Kilauea Volcano, Hawaii, 2007-2010

Kīlauea Volcano has one of the longest running volcanic sulfur dioxide (SO 2 ) emission rate databases on record. Sulfur dioxide emission rates from Kīlauea Volcano were first measured by Stoiber and Malone (1975) and have been measured on a regular basis since 1979 (Elias and Sutton, 2007, and references within). Compilations of SO 2 emission-rate and wind-vector data from 1979 through 2006 are available on the USGS Web site (Elias and others, 1998; Elias and Sutton, 2002; Elias and Sutton, 2007). This report updates the database, documents the changes in data collection and processing methods, and highlights how SO 2 emissions have varied with eruptive activity at Kīlauea Volcano for the interval 2007–2010.

Hawai'i↗
USGS2007

Sulfur dioxide emission rates from Kīlauea Volcano, Hawai‘i, an update: 2002-2006

Introduction Sulfur dioxide (SO 2 ) emission rates from Kilauea Volcano were first measured by Stoiber and Malone (1975) and have been measured on a regular basis since 1979 (Greenland and others, 1985; Casadevall and others, 1987; Elias and others, 1998; Sutton and others, 2001, Elias and Sutton, 2002, Sutton and others, 2003). Compilations of SO2 emission-rate and wind-vector data from 1979 through 2001 are available on the web. (Elias and others, 1998 and 2002). This report updates the database through 2006, and documents the changes in data collection and processing that have occurred during the interval 2002-2006. During the period covered by this report, Kilauea continued to release SO 2 gas predominantly from its summit caldera and east rift zone (ERZ) (Elias and others, 1998; Sutton and others, 2001, Elias and others, 2002, Sutton and others, 2003). These two distinct sources are always measured independently (fig.1). Sulphur Banks is a minor source of SO 2 and does not contribute significantly to the total emissions for Kilauea (Stoiber and Malone, 1975). From 1979 until 2003, summit and east rift zone emission rates were derived using vehicle- and tripod- based Correlation Spectrometry (COSPEC) measurements. In late 2003, we began to augment traditional COSPEC measurements with data from one of the new generation of miniature spectrometer systems, the FLYSPEC (Horton and others, 2006; Elias and others, 2006, Williams-Jones and others, 2006).

Hawaii↗
USGS2006

Puhimau thermal area: a window into the upper east rift zone of Kilauea Volcano, Hawaii?

We report the results of two soil CO 2 efflux surveys by the closed chamber circulation method at the Puhimau thermal area in the upper East Rift Zone (ERZ) of Kilauea volcano, Hawaii. The surveys were undertaken in 1996 and 1998 to constrain how much CO 2 might be reaching the ERZ after degassing beneath the summit caldera and whether the Puhimau thermal area might be a significant contributor to the overall CO 2 budget of Kilauea. The area was revisited in 2001 to determine the effects of surface disturbance on efflux values by the collar emplacement technique utilized in the earlier surveys. Utilizing a cutoff value of 50 g m −2 d −1 for the surrounding forest background efflux, the CO 2 emission rates for the anomaly at Puhimau thermal area were 27 t d −1 in 1996 and 17 t d −1 in 1998. Water vapor was removed before analysis in all cases in order to obtain CO 2 values on a dry air basis and mitigate the effect of water vapor dilution on the measurements. It is clear that Puhimau thermal area is not a significant contributor to Kilauea's CO 2 output and that most of Kilauea's CO 2 (8500 t d −1 ) is degassed at the summit, leaving only magma with its remaining stored volatiles, such as SO 2 , for injection down the ERZ. Because of the low CO 2 emission rate and the presence of a shallow water table in the upper ERZ that effectively scrubs SO 2 and other acid gases, Puhimau thermal area currently does not appear to be generally well suited for observing temporal changes in degassing at Kilauea.

Hawaii↗
USGS2002

Carbon dioxide emission rate of Kīlauea Volcano: Implications for primary magma and the summit reservoir

We report a CO 2 emission rate of 8500 metric tons per day (t d −1 ) for the summit of Kīlauea Volcano, several times larger than previous estimates. It is based on three sets of measurements over 4 years of synchronous SO 2 emission rates and volcanic CO 2 /SO 2 concentration ratios for the summit correlation spectrometer (COSPEC) traverse. Volcanic CO 2 /SO 2 for the traverse is representative of the global ratio for summit emissions. The summit CO 2 emission rate is nearly constant, despite large temporal variations in summit CO 2 /SO 2 and SO 2 emission rates. Summit CO 2 emissions comprise most of Kīlauea's total CO 2 output (∼9000 t d −1 ). The bulk CO 2 content of primary magma determined from CO 2 emission and magma supply rate data is ∼0.70 wt %. Most of the CO 2 is present as exsolved vapor at summit reservoir depths, making the primary magma strongly buoyant. Turbulent mixing with resident reservoir magma, however, prevents frequent eruptions of buoyant primary magma in the summit region. CO 2 emissions confirm that the magma supply enters the edifice through the summit reservoir. A persistent several hundred parts per million CO 2 anomaly arises from the entry of magma into the summit reservoir beneath a square kilometer area east of Halemaumau pit crater. Since most of the CO 2 in primary magma is degassed in the summit, the summit CO 2 emission rate is an effective proxy for the magma supply rate. Both scrubbing of SO 2 and solubility controls on CO 2 and S in basaltic melt cause high CO 2 /SO 2 in summit emissions and spatially uncorrelated distributions of CO 2 and SO 2 in the summit plume.

Journal of Geophysical Research B: Solid Earth↗
USGS2002

Sun photometer and lidar measurements of the plume from the Hawaii Kilauea Volcano Pu'u O'o vent: Aerosol flux and SO2 lifetime

Aerosol optical depths and lidar measurements were obtained under the plume of Hawaii Kilauea Volcano on August 17, 2001, ∼9 km downwind from the erupting Pu'u O'o vent. Measured aerosol optical depths (at 500 nm) were between 0.2–0.4. Aerosol size distributions inverted from the spectral sun photometer measurements suggest the volcanic aerosol is present in the accumulation mode (0.1–0.5 micron diameter), which is consistent with past in situ optical counter measurements. The aerosol dry mass flux rate was calculated to be 53 Mg d −1 . The estimated SO 2 emission rate during the aerosol measurements was ∼1450 Mg d −1 . Assuming the sulfur emissions at Pu'u O'o vent are mainly SO 2 (not aerosol), this corresponds to a SO 2 half-life of 6.0 hours in the atmosphere.

Hawaii↗
USGS2001

Implications for eruptive processes as indicated by sulfur dioxide emissions from Kilauea Volcano, Hawai'i, 1979-1997

Kı̄lauea Volcano, Hawai‘i, currently hosts the longest running SO 2 emission-rate data set on the planet, starting with initial surveys done in 1975 by Stoiber and his colleagues. The 17.5-year record of summit emissions, starting in 1979, shows the effects of summit and east rift eruptive processes, which define seven distinctly different periods of SO 2 release. Summit emissions jumped nearly 40% with the onset (3 January 1983) of the Pu`u `Ō`ō-Kūpaianaha eruption on the east rift zone (ERZ). Summit SO 2 emissions from Kı̄lauea showed a strong positive correlation with short-period, shallow, caldera events, rather than with long-period seismicity as in more silicious systems. This correlation suggests a maturation process in the summit magma-transport system from 1986 through 1993. During a steady-state throughput-equilibrium interval of the summit magma reservoir, integration of summit-caldera and ERZ SO 2 emissions reveals an undegassed volume rate of effusion of 2.1×10 5 m 3 /d. This value corroborates the volume-rate determined by geophysical methods, demonstrating that, for Kı̄lauea, SO 2 emission rates can be used to monitor effusion rate, supporting and supplementing other, more established geophysical methods. For the 17.5 years of continuous emission rate records at Kı̄lauea, the volcano has released 9.7×10 6 t (metric tonnes) of SO 2 , 1.7×10 6 t from the summit and 8.0×10 6 t from the east rift zone. On an annual basis, the average SO 2 release from Kı̄lauea is 4.6×10 5 t/y, compared to the global annual volcanic emission rate of 1.2×10 7 t/y.

Journal of Volcanology and Geothermal Research↗
USGS1998

Sulfur dioxide emission rates of Kilauea Volcano, Hawaii, 1979-1997

Sulfur dioxide (SO 2 ) emission rates from Kilauea Volcano were first measured by Stoiber and Malone (1975) and have been measured on a regular basis since 1979 (Casadevall and others, 1987; Greenland and others, 1985; Elias and others, 1993; Elias and Sutton, 1996). The purpose of this report is to present a compilation of Kilauea SO 2 emission rate data from 1979 through 1997 with ancillary meteorological data (wind speed and wind direction). We have included measurements previously reported by Casadevall and others (1987) for completeness and to improve the usefulness of this current database compilation. Kilauea releases SO 2 gas predominantly from its summit caldera and rift zones (fig. 1). From 1979 through 1982, vehicle-based COSPEC measurements made within the summit caldera were adequate to quantify most of the SO 2 emitted from the volcano. Beginning in 1983. the focus of SO 2 release shifted from the summit to the east rift zone (ERZ) eruption site at Pu'u 'O'o and, later, Kupaianaha. Since 1984, the Kilauea gas measurement effort has been augmented with intermittent airborne and tripod-based surveys made near the ERZ eruption site. In addition, beginning in 1992 vehicle-based measurements have been made along a section of Chain of Craters Road approximately 9 km downwind of the eruption site. These several types of COSPEC measurements continue to the present.

Hawaii↗
USGS1997

Multispectral thermal infrared mapping of sulfur dioxide plumes: A case study from the East Rift Zone of Kilauea Volcano, Hawaii

The synoptic perspective and rapid mode of data acquisition provided by remote sensing are well suited for the study of volcanic SO 2 plumes. In this paper we describe a plume-mapping procedure that is based on image data acquired with NASA's airborne thermal infrared multispectral scanner (TIMS) and apply the procedure to TIMS data collected over the East Rift Zone of Kilauea Volcano, Hawaii, on September 30, 1988. These image data covered the Pu‘u ‘O ‘o and Kupaianaha vents and a skylight in the lava tube that was draining the Kupaianaha lava pond. Our estimate of the SO 2 emission rate from Pu‘u ‘O ‘o (17–20 kg s −1 ) is roughly twice the average of estimates derived from correlation spectrometer (COSPEC) measurements collected 10 days prior to the TIMS overflight (10 kg s −1 ). The agreement between the TIMS and COSPEC results improves when we compare SO 2 burden estimates, which are relatively independent of wind speed. We demonstrate the feasibility of mapping Pu‘u ‘O ‘o - scale SO 2 plumes from space in anticipation of the 1998 launch of the advanced spaceborne thermal emission and reflectance radiometer (ASTER).

Journal of Geophysical Research B: Solid Earth↗
USGS1994

Eruptive activity at Mount St Helens, Washington, USA, 1984-1988: a gas geochemistry perspective

The results from two different types of gas measurement, telemetered in situ monitoring of reducing gases on the dome and airborne measurements of sulfur dioxide emission rates in the plume by correlation spectrometry, suggest that the combination of these two methods is particularly effective in detecting periods of enhanced degassing that intermittently punctuate the normal background leakage of gaseous effluent from Mount St Helens to the atmosphere. Gas events were recorded before lava extrusion for each of the four dome-building episodes at Mount St Helens since mid-1984. For two of the episodes, precursory reducing gas peaks were detected, whereas during three of the episodes, COSPEC measurements recorded precursory degassing of sulfur dioxide. During one episode (October 1986), both reducing gas monitoring and SO2 emission rate measurements simultaneously detected a large gas release several hours before lava extrusion. Had both types of gas measurements been operational during each of the dome-building episodes, it is thought that both would have recorded precursory signals for all four episodes. Evidence from the data presented herein suggests that increased degassing at Mount St Helens becomes detectable when fresh upward-moving magma is between 2 km and a few hundred meters below the base of the dome and between about 60 and 12 hours before the surface extrusion of lava. ?? 1994 Springer-Verlag.

Bulletin of Volcanology↗