Geology topics

Tamar Elias

Publications and source records attributed to Tamar Elias.

At least 37 records · Page 2Linked to original sources

USGS2017

Volcanic air pollution hazards in Hawaii

N oxious sulfur dioxide gas and other air pollutants emitted from Kīlauea Volcano on the Island of Hawai‘i react with oxygen, atmospheric moisture, and sunlight to produce volcanic smog (vog) and acid rain. Vog can negatively affect human health and agriculture, and acid rain can contaminate household water supplies by leaching metals from building and plumbing materials in rooftop rainwater-catchment systems. U.S. Geological Survey scientists, along with health professionals and local government officials are working together to better understand volcanic air pollution and to enhance public awareness of this hazard.

Hawaii↗

USGS2016

The 2014 annual report for the Hawaiian Volcano Observatory

Introduction This report summarizes team activities and findings of the Hawaiian Volcano Observatory during the year 2014 in geology, geodesy, seismicity, and gas geochemistry. The eruption of Pu‘u ‘Ō‘ō continued into its 32nd year with flows active to the northeast of the vent. One of them, the June 27th lava flow, named for the date in 2014 that the flow started, advanced far and fast enough to threaten the town of Pāhoa and Highway 130 in the Puna District of the Island of Hawai‘i. In response, the alert level for Kīlauea was elevated from WATCH to WARNING on September 4, followed by the declaration of a State Disaster on September 5 and a National Disaster on November 3. During 2014, renewed inflation and increased seismicity was detected beneath the summit and upper west flank of Mauna Loa. Although above background, the frequency and magnitude of the earthquakes remained at such low levels that, by year’s end, the four-tier alert level code for Mauna Loa remained at its lowest level—NORMAL. These changes were discussed in several Volcano Watch articles. Hualālai, Haleakalā, Mauna Kea, and Lo‘īhi showed no signs of unrest during the year.

Scientific Investigations Report↗

USGS2016

The 2014-2015 Pāhoa lava flow crisis at Kīlauea Volcano, Hawai‘i: Disaster avoided and lessons learned

Lava flow crises are nothing new on the Island of Hawai‘i, where their destructive force has been demonstrated repeatedly over the past several hundred years. The 2014–2015 Pāhoa lava flow crisis, however, was unique in terms of its societal impact and volcanological characteristics. Despite low effusion rates, a long-lived lava flow whose extent reached 20 km (the longest at Kīlauea Volcano in the past several hundred years) was poised for months to impact thousands of people, although direct impacts were ultimately minor (thus far). Careful observation of the flow reaffirmed and expanded knowledge of the processes associated with pāhoehoe emplacement, including the direct correlation between summit pressurization and flow advance, the influence of existing geologic structures on flow pathways, and the possible relationship between effusion rate and flow length. Communicating uncertainty associated with lava flow hazards was a challenge throughout the crisis, but online distribution of information and direct contact with residents proved to be effective strategies for keeping the public informed and educated about flow progress and how lava flows work (including forecasting limitations). Volcanological and sociological lessons will be important for inevitable future lava flow crises in Hawai‘i and, potentially, elsewhere in the world.

Hawaii↗

USGS2016

Volcanic air pollution over the Island of Hawai'i: Emissions, dispersal, and composition. Association with respiratory symptoms and lung function in Hawai'i Island school children

Background Kilauea Volcano on the Island of Hawai'i has erupted continuously since 1983, releasing approximately 300–12000 metric tons per day of sulfur dioxide (SO 2 ). SO 2 interacts with water vapor to produce an acidic haze known locally as “vog”. The combination of wind speed and direction, inversion layer height, and local terrain lead to heterogeneous and variable distribution of vog over the island, allowing study of respiratory effects associated with chronic vog exposure. Objectives We characterized the distribution and composition of vog over the Island of Hawai'i, and tested the hypotheses that chronic vog exposure (SO 2 and acid) is associated with increased asthma prevalence, respiratory symptoms, and reduced pulmonary function in Hawai'i Island schoolchildren. Methods We compiled data of volcanic emissions, wind speed, and wind direction over Hawai'i Island since 1992. Community-based researchers then measured 2- to 4-week integrated concentrations of SO 2 and fine particulate mass and acidity in 4 exposure zones, from 2002 to 2005, when volcanic SO 2 emissions averaged 1600 metric tons per day. Concurrently, community researchers recruited schoolchildren in the 4th and 5th grades of 25 schools in the 4 vog exposure zones, to assess determinants of lung health, respiratory symptoms, and asthma prevalence. Results Environmental data suggested 4 different vog exposure zones with SO 2 , PM2.5, and particulate acid concentrations (mean ± s.d.) as follows: 1) Low (0.3 ± 0.2 ppb, 2.5 ± 1.2 μg/m 3 , 0.6 ± 1.1 nmol H +/m 3 ), 2) Intermittent (1.6 ± 1.8 ppb, 2.8 ± 1.5 μg/m 3 , 4.0 ± 6.6 nmol H +/m 3 ), 3) Frequent (10.1 ± 5.2 ppb, 4.8 ± 1.9 μg/m 3 , 4.3 ± 6.7 nmol H +/m 3 ), and 4) Acid (1.2 ± 0.4 ppb, 7.2 ± 2.3 μg/m 3 , 25.3 ± 17.9 nmol H +/m 3 ). Participants (1957) in the 4 zones differed in race, prematurity, maternal smoking during pregnancy, environmental tobacco smoke exposure, presence of mold in the home, and physician-diagnosed asthma. Multivariable analysis showed an association between Acid vog exposure and cough and strongly suggested an association with FEV1/FVC < 0.8, but not with diagnosis of asthma, or chronic persistent wheeze or bronchitis in the last 12 months. Conclusions: Hawai'i Island's volcanic air pollution can be very acidic, but contains few co-contaminants originating from anthropogenic sources of air pollution. Chronic exposure to acid vog is associated with increased cough and possibly with reduced FEV1/FVC, but not with asthma or bronchitis. Further study is needed to better understand how volcanic air pollution interacts with host and environmental factors to affect respiratory symptoms, lung function, and lung growth, and to determine acute effects of episodes of increased emissions.

Hawai'i↗

USGS2015

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↗

USGS2015

Onset of a basaltic explosive eruption from Kīlauea’s summit in 2008

The onset of a basaltic eruption at the summit of Kīlauea volcano in 2008 is recorded in the products generated during the first three weeks of the eruption and suggests an evolution of both the physical properties of the magma and also lava lake levels and vent wall stability. Ash componentry and the microtextures of the early erupted lapilli products reveal that the magma was largely outgassed, perhaps in the preceding weeks to months. An increase in the juvenile:lithic ratio and size of ash collected from March 23 to April 3 records an increasing level of the magma within the conduit. After April 3 until the explosive eruption of April 9, a trend of decreasing juvenile:lithic ratio suggests that vent wall collapses were more frequent, possibly because lava level increased and destabilized the overhanging wall [Orr et al. 2013]. Despite increasing lake height, the microtextural characteristics of the lapilli suggest that the outgassed end-member was still being tapped between March 26 and April 8. The April 9 rockfall triggered an explosive eruption that produced a new component in the eruption deposits not seen in the preceding weeks; microvesicular juvenile lapilli, the first evidence of an actively vesiculating magma. Two additional dense end-member pyroclast types were also erupted during the April 9 explosion, likely related to outgassed magma with longer residence times than the microvesicular magma. We link these pyroclasts to a stagnant viscous crust at the top of the magma column or to convecting, downwelling magma. Our study of ash componentry and the textures of juvenile lapilli suggests that the April 9 explosive event effectively cleared the conduit of largely outgassed magma. The degassing processes during this eruption are complex and varied: in the period of persistent degassing during March 26-April 8 small resident bubbles at shallow levels in the lava lake were coupled to the magma whereas large bubbles ascended, expanded and fragmented. During the rockfall- triggered explosion of April 9, all bubbles were coupled to the host magma on the timescale of decompression, but additional exsolution, decompression and expansion of deeper, more gas-rich resident magma likely occurred [cf. Carey et al. 2012]. Where external conditions play a significant role in eruption dynamics, e.g., by triggering eruptions, vesiculation and degassing dynamics can be expected to be complex.

Hawai'i↗

USGS2015

An automated SO2 camera system for continuous, real-time monitoring of gas emissions from Kīlauea Volcano's summit Overlook Crater

SO 2 camera systems allow rapid two-dimensional imaging of sulfur dioxide (SO 2 ) emitted from volcanic vents. Here, we describe the development of an SO 2 camera system specifically designed for semi-permanent field installation and continuous use. The integration of innovative but largely “off-the-shelf” components allowed us to assemble a robust and highly customizable instrument capable of continuous, long-term deployment at Kīlauea Volcano's summit Overlook Crater. Recorded imagery is telemetered to the USGS Hawaiian Volcano Observatory (HVO) where a novel automatic retrieval algorithm derives SO 2 column densities and emission rates in real-time. Imagery and corresponding emission rates displayed in the HVO operations center and on the internal observatory website provide HVO staff with useful information for assessing the volcano's current activity. The ever-growing archive of continuous imagery and high-resolution emission rates in combination with continuous data from other monitoring techniques provides insight into shallow volcanic processes occurring at the Overlook Crater. An exemplary dataset from September 2013 is discussed in which a variation in the efficiency of shallow circulation and convection, the processes that transport volatile-rich magma to the surface of the summit lava lake, appears to have caused two distinctly different phases of lake activity and degassing. This first successful deployment of an SO 2 camera for continuous, real-time volcano monitoring shows how this versatile technique might soon be adapted and applied to monitor SO 2 degassing at other volcanoes around the world.

Hawai'i↗

USGS2015

Using SO 2 camera imagery and seismicity to examine degassing and gas accumulation at Kīlauea Volcano, May 2010

SO 2 camera measurements at Kīlauea Volcano, Hawaii, in May of 2010 captured two occurrences of lava lake rise and fall within the Halema'um'au Crater summit vent. During high lava stands we observed diminished SO 2 emission rates and decreased seismic tremor. Similar events at Kīlauea have been described as the result of sporadic degassing following gas accumulation beneath a mostly impermeable lava lake surface. Incorporation of SO 2 camera data into a multi-parameter dataset gives credence to the likelihood of shallow gas accumulation as the cause of these high stand events, with accumulated gas release upon lake-level drop compensating for the gas deficit reached during accumulation.

Hawaii↗

USGS2014

One hundred volatile years of volcanic gas studies at the Hawaiian Volcano Observatory

The first volcanic gas studies in Hawai‘i, beginning in 1912, established that volatile emissions from Kīlauea Volcano contained mostly water vapor, in addition to carbon dioxide and sulfur dioxide. This straightforward discovery overturned a popular volatile theory of the day and, in the same action, helped affirm Thomas A. Jaggar, Jr.’s, vision of the Hawaiian Volcano Observatory (HVO) as a preeminent place to study volcanic processes. Decades later, the environmental movement produced a watershed of quantitative analytical tools that, after being tested at Kīlauea, became part of the regular monitoring effort at HVO. The resulting volatile emission and fumarole chemistry datasets are some of the most extensive on the planet. These data indicate that magma from the mantle enters the shallow magmatic system of Kīlauea sufficiently oversaturated in CO 2 to produce turbulent flow. Passive degassing at Kīlauea’s summit that occurred from 1983 through 2007 yielded CO 2 -depleted, but SO 2 - and H 2 O-rich, rift eruptive gases. Beginning with the 2008 summit eruption, magma reaching the East Rift Zone eruption site became depleted of much of its volatile content at the summit eruptive vent before transport to Pu‘u ‘Ō‘ō. The volatile emissions of Hawaiian volcanoes are halogen-poor, relative to those of other basaltic systems. Information gained regarding intrinsic gas solubilities at Kīlauea and Mauna Loa, as well as the pressure-controlled nature of gas release, have provided useful tools for tracking eruptive activity. Regular CO 2 -emission-rate measurements at Kīlauea’s summit, together with surface-deformation and other data, detected an increase in deep magma supply more than a year before a corresponding surge in effusive activity. Correspondingly, HVO routinely uses SO 2 emissions to study shallow eruptive processes and effusion rates. HVO gas studies and Kīlauea’s long-running East Rift Zone eruption also demonstrate that volatile emissions can be a substantial volcanic hazard in Hawai‘i. From its humble beginning, trying to determine the chemical composition of volcanic gases over a century ago, HVO has evolved to routinely use real-time gas chemistry to track eruptive processes, as well as hazards.

Hawaii↗

USGS2013

Applying UV cameras for SO 2 detection to distant or optically thick volcanic plumes

Ultraviolet (UV) camera systems represent an exciting new technology for measuring two dimensional sulfur dioxide (SO 2 ) distributions in volcanic plumes. The high frame rate of the cameras allows the retrieval of SO 2 emission rates at time scales of 1 Hz or higher, thus allowing the investigation of high-frequency signals and making integrated and comparative studies with other high-data-rate volcano monitoring techniques possible. One drawback of the technique, however, is the limited spectral information recorded by the imaging systems. Here, a framework for simulating the sensitivity of UV cameras to various SO 2 distributions is introduced. Both the wavelength-dependent transmittance of the optical imaging system and the radiative transfer in the atmosphere are modeled. The framework is then applied to study the behavior of different optical setups and used to simulate the response of these instruments to volcanic plumes containing varying SO 2 and aerosol abundances located at various distances from the sensor. Results show that UV radiative transfer in and around distant and/or optically thick plumes typically leads to a lower sensitivity to SO 2 than expected when assuming a standard Beer–Lambert absorption model. Furthermore, camera response is often non-linear in SO 2 and dependent on distance to the plume and plume aerosol optical thickness and single scatter albedo. The model results are compared with camera measurements made at Kilauea Volcano (Hawaii) and a method for integrating moderate resolution differential optical absorption spectroscopy data with UV imagery to retrieve improved SO 2 column densities is discussed.

Journal of Volcanology and Geothermal Research↗

USGS2013

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↗

USGS2012

Improving the accuracy of S0 2 column densities and emission rates obtained from upward-looking UV-spectroscopic measurements of volcanic plumes by taking realistic radiative transfer into account

Sulfur dioxide (SO 2 ) is monitored using ultraviolet (UV) absorption spectroscopy at numerous volcanoes around the world due to its importance as a measure of volcanic activity and a tracer for other gaseous species. Recent studies have shown that failure to take realistic radiative transfer into account during the spectral retrieval of the collected data often leads to large errors in the calculated emission rates. Here, the framework for a new evaluation method which couples a radiative transfer model to the spectral retrieval is described. In it, absorption spectra are simulated, and atmospheric parameters are iteratively updated in the model until a best match to the measurement data is achieved. The evaluation algorithm is applied to two example Differential Optical Absorption Spectroscopy (DOAS) measurements conducted at Kilauea volcano (Hawaii). The resulting emission rates were 20 and 90% higher than those obtained with a conventional DOAS retrieval performed between 305 and 315 nm, respectively, depending on the different SO 2 and aerosol loads present in the volcanic plume. The internal consistency of the method was validated by measuring and modeling SO2 absorption features in a separate wavelength region around 375 nm and comparing the results. Although additional information about the measurement geometry and atmospheric conditions is needed in addition to the acquired spectral data, this method for the first time provides a means of taking realistic three-dimensional radiative transfer into account when analyzing UV-spectral absorption measurements of volcanic SO 2 plumes.

Journal of Geophysical Research D: Atmospheres↗

USGS2011

Small explosion from new vent at Kilauea’s summit

At 0258 Hawaii‐Aleutian Standard Time (HST) on 19 March 2008, a small explosion scattered altered and fresh lithic debris across a 40‐hectare area at the summit of Kilauea volcano. This explosion, the first recorded there since 1924, issued from a vent about 35 meters wide along the east wall of Halema'uma'u Crater. Ballistic fragments—the largest measuring nearly 1 meter across—were propelled upward more than 70 meters onto the Halema'uma'u crater rim. Coarse ash and centimeter‐size lithic debris covered part of Crater Rim Drive, and fine ash was deposited farther than 30 kilometers to the southwest.

Hawaii↗

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

Comparison of COSPEC and two miniature ultraviolet spectrometer systems for SO 2 measurements using scattered sunlight

The correlation spectrometer (COSPEC), the principal tool for remote measurements of volcanic SO 2 , is rapidly being replaced by low-cost, miniature, ultraviolet (UV) spectrometers. We compared two of these new systems with a COSPEC by measuring SO 2 column amounts at Kīlauea Volcano, Hawaii. The two systems, one calibrated using in-situ SO 2 cells, and the other using a calibrated laboratory reference spectrum, employ similar spectrometer hardware, but different foreoptics and spectral retrieval algorithms. Accuracy, signal-to-noise, retrieval parameters, and precision were investigated for the two configurations of new miniature spectrometer. Measurements included traverses beneath the plumes from the summit and east rift zone of Kīlauea, and testing with calibration cells of known SO 2 concentration. The results obtained from the different methods were consistent with each other, with <8% difference in estimated SO 2 column amounts up to 800 ppm m. A further comparison between the COSPEC and one of the miniature spectrometer configurations, the ‘FLYSPEC’, spans an eight month period and showed agreement of measured emission rates to within 10% for SO 2 column amounts up to 1,600 ppm m. The topic of measuring high SO 2 burdens accurately is addressed for the Kīlauea measurements. In comparing the foreoptics, retrieval methods, and resultant implications for data quality, we aim to consolidate the various experiences to date, and improve the application and development of miniature spectrometer systems.`

Bulletin of Volcanology↗

USGS2005

Accurately measuring volcanic plume velocity with multiple UV spectrometers

A fundamental problem with all ground-based remotely sensed measurements of volcanic gas flux is the difficulty in accurately measuring the velocity of the gas plume. Since a representative wind speed and direction are used as proxies for the actual plume velocity, there can be considerable uncertainty in reported gas flux values. Here we present a method that uses at least two time-synchronized simultaneously recording UV spectrometers (FLYSPECs) placed a known distance apart. By analyzing the time varying structure of SO 2 concentration signals at each instrument, the plume velocity can accurately be determined. Experiments were conducted on Kīlauea (USA) and Masaya (Nicaragua) volcanoes in March and August 2003 at plume velocities between 1 and 10 m s −1 . Concurrent ground-based anemometer measurements differed from FLYSPEC-measured plume speeds by up to 320%. This multi-spectrometer method allows for the accurate remote measurement of plume velocity and can therefore greatly improve the precision of volcanic or industrial gas flux measurements.

Kīlauea volcano, Masaya volcano↗

USGS2005

Real-time measurement of volcanic SO 2 emissions: Validation of a new UV correlation spectrometer (FLYSPEC)

A miniaturized, lightweight and low-cost UV correlation spectrometer, the FLYSPEC, has been developed as an alternative for the COSPEC, which has long been the mainstay for monitoring volcanic sulfur dioxide fluxes. Field experiments have been conducted with the FLYSPEC at diverse volcanic systems, including Masaya (Nicaragua), Poás (Costa Rica), Stromboli, Etna and Vulcano (Italy), Villarica (Chile) and Kilauea (USA). We present here those validation measurements that were made simultaneously with COSPEC at Kilauea between March 2002 and February 2003. These experiments, with source emission rates that ranged from 95 to 1,560 t d −1 , showed statistically identical results from both instruments. SO 2 path-concentrations ranged from 0 to >1,000 ppm-m with average correlation coefficients greater than r 2 =0.946. The small size and low cost create the opportunity for FLYSPEC to be used in novel deployment modes that have the potential to revolutionize the manner in which volcanic and industrial monitoring is performed.

Bulletin of Volcanology↗

USGS2005

Reconnaissance gas measurements on the East Rift Zone of Kilauea Volcano, Hawai'i by Fourier transform infrared spectroscopy

We report the results of a set of measurements of volcanic gases on two small ground level plumes in the vicinity of Pu`u `O`o cone on the middle East Rift Zone (ERZ) of Kilauea volcano, Hawai`i on 15 June 2001 using open-path Fourier transform infrared (FTIR) spectroscopy. The work was carried out as a reconnaissance survey to assess the monitoring and research value of FTIR measurements at this volcano. Despite representing emissions of residual volatiles from lava that has undergone prior degassing, the plumes contained detectable amounts of CO2, CO, SO2, HCl, HF and SiF4. Various processes, including subsurface cooling, condensation of water in the atmospheric plume, oxidation, dissolution in water, and reactions with wall rocks at plume vents affect the abundance of these gases. Low concentrations of volcanic CO2 measured against a high ambient background are not well constrained by FTIR spectroscopy. Although there appear to be some differences between these gases and Pu`u `O`o source gases, ratios of HCl/SO2, HF/SO2 and CO/SO2 determined by FTIR measurements of these two small plumes compare reasonably well with earlier published analyses of ERZ vent samples. The measurements yielded emission rate estimates of 4, 11 and 4 t d-1

Hawaii↗