Volcanic Plume Measurements with UAV (Invited)

Science.gov (United States)

Shinohara, H.; Kaneko, T.; Ohminato, T.

2013-12-01

Volatiles in magmas are the driving force of volcanic eruptions and quantification of volcanic gas flux and composition is important for the volcano monitoring. Recently we developed a portable gas sensor system (Multi-GAS) to quantify the volcanic gas composition by measuring volcanic plumes and obtained volcanic gas compositions of actively degassing volcanoes. As the Multi-GAS measures variation of volcanic gas component concentrations in the pumped air (volcanic plume), we need to bring the apparatus into the volcanic plume. Commonly the observer brings the apparatus to the summit crater by himself but such measurements are not possible under conditions of high risk of volcanic eruption or difficulty to approach the summit due to topography etc. In order to overcome these difficulties, volcanic plume measurements were performed by using manned and unmanned aerial vehicles. The volcanic plume measurements by manned aerial vehicles, however, are also not possible under high risk of eruption. The strict regulation against the modification of the aircraft, such as installing sampling pipes, also causes difficulty due to the high cost. Application of the UAVs for the volcanic plume measurements has a big advantage to avoid these problems. The Multi-GAS consists of IR-CO2 and H2O gas analyzer, SO2-H2O chemical sensors and H2 semiconductor sensor and the total weight ranges 3-6 kg including batteries. The necessary conditions of the UAV for the volcanic plumes measurements with the Multi-GAS are the payloads larger than 3 kg, maximum altitude larger than the plume height and installation of the sampling pipe without contamination of the exhaust gases, as the exhaust gases contain high concentrations of H2, SO2 and CO2. Up to now, three different types of UAVs were applied for the measurements; Kite-plane (Sky Remote) at Miyakejima operated by JMA, Unmanned airplane (Air Photo Service) at Shinomoedake, Kirishima volcano, and Unmanned helicopter (Yamaha) at Sakurajima

Applying UV cameras for SO2 detection to distant or optically thick volcanic plumes

Science.gov (United States)

Kern, Christoph; Werner, Cynthia; Elias, Tamar; Sutton, A. Jeff; Lübcke, Peter

2013-01-01

Ultraviolet (UV) camera systems represent an exciting new technology for measuring two dimensional sulfur dioxide (SO2) distributions in volcanic plumes. The high frame rate of the cameras allows the retrieval of SO2 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 SO2 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 SO2 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 SO2 than expected when assuming a standard Beer–Lambert absorption model. Furthermore, camera response is often non-linear in SO2 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 SO2 column densities is discussed.

Recent advances in ground-based ultraviolet remote sensing of volcanic SO2 fluxes

Directory of Open Access Journals (Sweden)

Euripides P. Kantzas

2011-06-01

Full Text Available Measurements of volcanic SO2 emission rates have been the mainstay of remote-sensing volcanic gas geochemistry for almost four decades, and they have contributed significantly to our understanding of volcanic systems and their impact upon the atmosphere. The last ten years have brought step-change improvements in the instrumentation applied to these observations, which began with the application of miniature ultraviolet spectrometers that were deployed in scanning and traverse configurations, with differential optical absorption spectroscopy evaluation routines. This study catalogs the more recent empirical developments, including: ultraviolet cameras; wide-angle field-of-view differential optical absorption spectroscopy systems; advances in scanning operations, including tomography; and improved understanding of errors, in particular concerning radiative transfer. Furthermore, the outcomes of field deployments of sensors during the last decade are documented, with respect to improving our understanding of volcanic dynamics and degassing into the atmosphere.

Using CATS Near-Real-time Lidar Observations to Monitor and Constrain Volcanic Sulfur Dioxide (SO2) Forecasts

Science.gov (United States)

Hughes, E. J.; Yorks, J.; Krotkov, N. A.; da Silva, A. M.; Mcgill, M.

2016-01-01

An eruption of Italian volcano Mount Etna on 3 December 2015 produced fast-moving sulfur dioxide (SO2) and sulfate aerosol clouds that traveled across Asia and the Pacific Ocean, reaching North America in just 5 days. The Ozone Profiler and Mapping Suite's Nadir Mapping UV spectrometer aboard the U.S. National Polar-orbiting Partnership satellite observed the horizontal transport of the SO2 cloud. Vertical profiles of the colocated volcanic sulfate aerosols were observed between 11.5 and 13.5 km by the new Cloud Aerosol Transport System (CATS) space-based lidar aboard the International Space Station. Backward trajectory analysis estimates the SO2 cloud altitude at 7-12 km. Eulerian model simulations of the SO2 cloud constrained by CATS measurements produced more accurate dispersion patterns compared to those initialized with the back trajectory height estimate. The near-real-time data processing capabilities of CATS are unique, and this work demonstrates the use of these observations to monitor and model volcanic clouds.

Volcanic SO2 and SiF4 visualization using 2-D thermal emission spectroscopy – Part 1: Slant-columns and their ratios

Directory of Open Access Journals (Sweden)

M. Grutter

2012-02-01

Full Text Available The composition and emission rates of volcanic gas plumes provide insight of the geologic internal activity, atmospheric chemistry, aerosol formation and radiative processes around it. Observations are necessary for public security and the aviation industry. Ground-based thermal emission infrared spectroscopy, which uses the radiation of the volcanic gas itself, allows for continuously monitoring during day and night from a safe distance. We present measurements on Popocatépetl volcano based on thermal emission spectroscopy during different campaigns between 2006–2009 using a Scanning Infrared Gas Imaging System (SIGIS. The experimental set-up, measurement geometries and analytical algorithms are described. The equipment was operated from a safe distance of 12 km from the volcano at two different spectral resolutions: 0.5 and 4 cm−1. The 2-dimensional scanning capability of the instrument allows for an on-line visualization of the volcanic SO2 plume and its animation. SiF4 was also identified in the infrared spectra recorded at both resolutions. The SiF4/SO2 molecular ratio can be calculated from each image and used as a highly useful parameter to follow changes in volcanic activity. A small Vulcanian eruption was monitored during the night of 16 to 17 November 2008 and strong ash emission together with a pronounced SO2 cloud was registered around 01:00 a.m. LST (Local Standard Time. Enhanced SiF4/SO2 ratios were observed before and after the eruption. A validation of the results from thermal emission measurements with those from absorption spectra of the moon taken at the same time, as well as an error analysis, are presented. The inferred propagation speed from sequential images is used in a subsequent paper (Part 2 to calculate the emission rates at different distances from the crater.

Real-Time Estimation of Volcanic ASH/SO2 Cloud Height from Combined Uv/ir Satellite Observations and Numerical Modeling

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Vicente, Gilberto A.

An efficient iterative method has been developed to estimate the vertical profile of SO2 and ash clouds from volcanic eruptions by comparing near real-time satellite observations with numerical modeling outputs. The approach uses UV based SO2 concentration and IR based ash cloud images, the volcanic ash transport model PUFF and wind speed, height and directional information to find the best match between the simulated and the observed displays. The method is computationally fast and is being implemented for operational use at the NOAA Volcanic Ash Advisory Centers (VAACs) in Washington, DC, USA, to support the Federal Aviation Administration (FAA) effort to detect, track and measure volcanic ash cloud heights for air traffic safety and management. The presentation will show the methodology, results, statistical analysis and SO2 and Aerosol Index input products derived from the Ozone Monitoring Instrument (OMI) onboard the NASA EOS/Aura research satellite and from the Global Ozone Monitoring Experiment-2 (GOME-2) instrument in the MetOp-A. The volcanic ash products are derived from AVHRR instruments in the NOAA POES-16, 17, 18, 19 as well as MetOp-A. The presentation will also show how a VAAC volcanic ash analyst interacts with the system providing initial condition inputs such as location and time of the volcanic eruption, followed by the automatic real-time tracking of all the satellite data available, subsequent activation of the iterative approach and the data/product delivery process in numerical and graphical format for operational applications.

The primary volcanic aerosol emission from Mt Etna: Size-resolved particles with SO2 and role in plume reactive halogen chemistry

Science.gov (United States)

Roberts, T. J.; Vignelles, D.; Liuzzo, M.; Giudice, G.; Aiuppa, A.; Coltelli, M.; Salerno, G.; Chartier, M.; Couté, B.; Berthet, G.; Lurton, T.; Dulac, F.; Renard, J.-B.

2018-02-01

Volcanoes are an important source of aerosols to the troposphere. Within minutes after emission, volcanic plume aerosol catalyses conversion of co-emitted HBr, HCl into highly reactive halogens (e.g. BrO, OClO) through chemical cycles that cause substantial ozone depletion in the dispersing downwind plume. This study quantifies the sub-to-supramicron primary volcanic aerosol emission (0.2-5 μm diameter) and its role in this process. An in-situ ground-based study at Mt Etna (Italy) during passive degassing co-deployed an optical particle counter and Multi-Gas SO2 sensors at high time resolution (0.1 Hz) enabling to characterise the aerosol number, size-distribution and emission flux. A tri-modal volcanic aerosol size distribution was found, to which lognormal distributions are fitted. Total particle volume correlates to SO2 (as a plume tracer). The measured particle volume:SO2 ratio equates to a sulfate:SO2 ratio of 1-2% at the observed meteorological conditions (40% Relative Humidity). A particle mass flux of 0.7 kg s-1 is calculated for the measured Mt Etna SO2 flux of 1950 tonnes/day. A numerical plume atmospheric chemistry model is used to simulate the role of the hygroscopic primary aerosol surface area and its humidity dependence on volcanic plume BrO and OClO chemistry. As well as predicting volcanic BrO formation and O3 depletion, the model achieves OClO/SO2 in broad quantitative agreement with recently reported Mt Etna observations, with a predicted maximum a few minutes downwind. In addition to humidity - that enhances aerosols surface area for halogen cycling - background ozone is predicted to be an important control on OClO/SO2. Dependence of BrO/SO2 on ambient humidity is rather low near-to-source but increases further downwind. The model plume chemistry also exhibits strong across-plume spatial variations between plume edge and centre.

A Balloon Sounding Technique for Measuring SO2 Plumes

Science.gov (United States)

Morris, Gary A.; Komhyr, Walter D.; Hirokawa, Jun; Lefer, Barry; Krotkov, Nicholay; Ngan, Fong

2010-01-01

This paper reports on the development of a new technique for inexpensive measurements of SO2 profiles using a modified dual-ozonesonde instrument payload. The presence of SO2 interferes with the standard electrochemical cell (ECC) ozonesonde measurement, resulting in -1 molecule of O3 reported for each molecule of SO2 present (provided [O3] > [SO2]). In laboratory tests, an SO2 filter made with Cr03 placed on the inlet side of the sonde removes nearly 100% of the SO2 present for concentrations up to 60 ppbv and remained effective after exposure to 2.8 X 10(exp 16) molecules of SO2 [equivalent to a column approximately 150 DU (1 DU = 2.69 X 10(exp 20) molecules m(exp -2))]. Flying two ECC instruments on the same payload with one filtered and the other unfiltered yields SO2 profiles, inferred by subtraction. Laboratory tests and field experience suggest an SO2 detection limit of approximately 3 pbb with profiles valid from the surface to the ozonopause [i.e., approximately (8-10 km)]. Two example profiles demonstrate the success of this technique for both volcanic and industrial plumes.

Extended observations of volcanic SO2 and sulfate aerosol in the stratosphere

NARCIS (Netherlands)

Carn, S.A.; Krotkov, N.A.; Yang, Kai; Hoff, R.M.; Prata, A.J.; Krueger, A.J.; Loughlin, S.C.; Levelt, P.F.

2007-01-01

Sulfate aerosol produced after injection of sulfur dioxide (SO2) into the stratosphere by volcanic eruptions can trigger climate change. We present new satellite data from the Ozone Monitoring Instrument (OMI) and Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIPSO) missions

Measurements of SO2 in the Mount St. Helens debris

International Nuclear Information System (INIS)

Kerr, J.B.; Evans, F.J.; Mateer, C.L.

1982-01-01

Routine measurements of ozone and SO 2 are made with the Dobson and Brewer spectrophotometers at the Atmospheric Environment Service in Downsview Ontario. On May 20 and 21, 1980, large values of column SO 2 were observed with both spectrophotometers at the time of passage of the Mount St. Helens debris. Enhanced SO 2 values were first observed at 1800Z on May 20. The maximum column amount of SO 2 measured was 0.06 cm at 2200 Z. On May 21, SO 2 values slowly decreased from 0.03 cm at 1100 Z cm to 0.01 cm at 2000Z. Typical SO 2 amounts due to pollution at the Downsview site are approximately 0.003 to 0.005 cm. At the same time of maximum SO 2 enhancement, both Dobson and Brewer spectrophotometers measured a 0.040 cm decrease of total ozone. It is not clear whether the decrease of total ozone was caused by the volcanic cloud or natural ozone variability. Air mass trajectories indicate that the altitude of the debris cloud, which passed over Downsview at the time, was between 10 km and 12 km

Modeling of 2008 Kasatochi Volcanic Sulfate Direct Radiative Forcing: Assimilation of OMI SO2 Plume Height Data and Comparison with MODIS and CALIOP Observations

Science.gov (United States)

Wang, J.; Park, S.; Zeng, J.; Ge, C.; Yang, K.; Carn, S.; Krotkov, N.; Omar, A. H.

2013-01-01

Volcanic SO2 column amount and injection height retrieved from the Ozone Monitoring Instrument (OMI) with the Extended Iterative Spectral Fitting (EISF) technique are used to initialize a global chemistry transport model (GEOS-Chem) to simulate the atmospheric transport and lifecycle of volcanic SO2 and sulfate aerosol from the 2008 Kasatochi eruption, and to subsequently estimate the direct shortwave, top-of-the-atmosphere radiative forcing of the volcanic sulfate aerosol. Analysis shows that the integrated use of OMI SO2 plume height in GEOS-Chem yields: (a) good agreement of the temporal evolution of 3-D volcanic sulfate distributions between model simulations and satellite observations from the Moderate Resolution Imaging Spectroradiometer (MODIS) and Cloud-Aerosol Lidar with Orthogonal Polarisation (CALIOP), and (b) an e-folding time for volcanic SO2 that is consistent with OMI measurements, reflecting SO2 oxidation in the upper troposphere and stratosphere is reliably represented in the model. However, a consistent (approx. 25 %) low bias is found in the GEOS-Chem simulated SO2 burden, and is likely due to a high (approx.20 %) bias of cloud liquid water amount (as compared to the MODIS cloud product) and the resultant stronger SO2 oxidation in the GEOS meteorological data during the first week after eruption when part of SO2 underwent aqueous-phase oxidation in clouds. Radiative transfer calculations show that the forcing by Kasatochi volcanic sulfate aerosol becomes negligible 6 months after the eruption, but its global average over the first month is -1.3W/sq m, with the majority of the forcing-influenced region located north of 20degN, and with daily peak values up to -2W/sq m on days 16-17. Sensitivity experiments show that every 2 km decrease of SO2 injection height in the GEOS-Chem simulations will result in a approx.25% decrease in volcanic sulfate forcing; similar sensitivity but opposite sign also holds for a 0.03 m increase of geometric radius of

SO2 photoexcitation mechanism links mass-independent sulfur isotopic fractionation in cryospheric sulfate to climate impacting volcanism

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Hattori, Shohei; Schmidt, Johan A.; Johnson, Matthew S.; Danielache, Sebastian O.; Yamada, Akinori; Ueno, Yuichiro; Yoshida, Naohiro

2013-01-01

Natural climate variation, such as that caused by volcanoes, is the basis for identifying anthropogenic climate change. However, knowledge of the history of volcanic activity is inadequate, particularly concerning the explosivity of specific events. Some material is deposited in ice cores, but the concentration of glacial sulfate does not distinguish between tropospheric and stratospheric eruptions. Stable sulfur isotope abundances contain additional information, and recent studies show a correlation between volcanic plumes that reach the stratosphere and mass-independent anomalies in sulfur isotopes in glacial sulfate. We describe a mechanism, photoexcitation of SO2, that links the two, yielding a useful metric of the explosivity of historic volcanic events. A plume model of S(IV) to S(VI) conversion was constructed including photochemistry, entrainment of background air, and sulfate deposition. Isotopologue-specific photoexcitation rates were calculated based on the UV absorption cross-sections of 32SO2, 33SO2, 34SO2, and 36SO2 from 250 to 320 nm. The model shows that UV photoexcitation is enhanced with altitude, whereas mass-dependent oxidation, such as SO2 + OH, is suppressed by in situ plume chemistry, allowing the production and preservation of a mass-independent sulfur isotope anomaly in the sulfate product. The model accounts for the amplitude, phases, and time development of Δ33S/δ34S and Δ36S/Δ33S found in glacial samples. We are able to identify the process controlling mass-independent sulfur isotope anomalies in the modern atmosphere. This mechanism is the basis of identifying the magnitude of historic volcanic events. PMID:23417298

Rates of volcanic CO2 degassing from airborne determinations of SO2 Emission rates and plume CO2SO2: test study at Pu′u ′O′o Cone, Kilauea Volcano, Hawaii

Science.gov (United States)

Gerlach, Terrence M.; McGee, Kenneth A.; Sutton, A. Jefferson; Elias, Tamar

1998-01-01

We present an airborne method that eliminates or minimizes several disadvantages of the customary plume cross-section sampling method for determining volcanic CO2 emission rates. A LI-COR CO2analyzer system (LICOR), a Fourier transform infrared spectrometer system (FTIR), and a correlation spectrometer (COSPEC) were used to constrain the plume CO2/SO2 and the SO2 emission rate. The method yielded a CO2 emission rate of 300 td−1 (metric tons per day) for Pu′u ′O′o cone, Kilauea volcano, on 19 September 1995. The CO2/SO2 of 0.20 determined from airborne LICOR and FTIR plume measurements agreed with the CO2/SO2 of 204 ground-based samples collected from vents over a 14-year period since the Pu′u ′O′o eruption began in January 1983.

Continuous SO2 flux measurements for Vulcano Island, Italy

Directory of Open Access Journals (Sweden)

Fabio Vita

2012-06-01

Full Text Available The La Fossa cone of Vulcano Island (Aeolian Archipelago, Italy is a closed conduit volcano. Today, Vulcano Island is characterized by sulfataric activity, with a large fumarolic field that is mainly located in the summit area. A scanning differential optical absorption spectroscopy instrument designed by the Optical Sensing Group of Chalmers University of Technology in Göteborg, Sweden, was installed in the framework of the European project "Network for Observation of Volcanic and Atmospheric Change", in March 2008. This study presents the first dataset of SO2 plume fluxes recorded for a closed volcanic system. Between 2008 and 2010, the SO2 fluxes recorded showed average values of 12 t.d–1 during the normal sulfataric activity of Vulcano Island, with one exceptional event of strong degassing that occurred between September and December, 2009, when the SO2 emissions reached up to 100 t.d–1.

Ground-based remote sensing of volcanic CO2 and correlated SO2, HF, HCl, and BrO, in safe-distance from the crater

Science.gov (United States)

Butz, Andre; Solvejg Dinger, Anna; Bobrowski, Nicole; Kostinek, Julian; Fieber, Lukas; Fischerkeller, Constanze; Giuffrida, Giovanni Bruno; Hase, Frank; Klappenbach, Friedrich; Kuhn, Jonas; Lübcke, Peter; Tirpitz, Lukas; Tu, Qiansi

2017-04-01

Remote sensing of CO2 enhancements in volcanic plumes can be a tool to estimate volcanic CO2 emissions and thereby, to gain insight into the geological carbon cycle and into volcano interior processes. However, remote sensing of the volcanic CO2 is challenged by the large atmospheric background concentrations masking the minute volcanic signal. Here, we report on a demonstrator study conducted in September 2015 at Mt. Etna on Sicily, where we deployed an EM27/SUN Fourier Transform Spectrometer together with a UV spectrometer on a mobile remote sensing platform. The spectrometers were operated in direct-sun viewing geometry collecting cross-sectional scans of solar absorption spectra through the volcanic plume by operating the platform in stop-and-go patterns in 5 to 10 kilometers distance from the crater region. We successfully detected correlated intra-plume enhancements of CO2 and volcanic SO2, HF, HCl, and BrO. The path-integrated volcanic CO2 enhancements amounted to about 0.5 ppm (on top of the ˜400 ppm background). Key to successful detection of volcanic CO2 was A) the simultaneous observation of the O2 total column which allowed for correcting changes in the CO2 column caused by changes in observer altitude and B) the simultaneous measurement of volcanic species co-emitted with CO2 which allowed for discriminating intra-plume and extra-plume observations. The latter were used for subtracting the atmospheric CO2 background. The field study suggests that our remote sensing observatory is a candidate technique for volcano monitoring in safe distance from the crater region.

Volcanic Ash and SO2 Monitoring Using Suomi NPP Direct Broadcast OMPS Data

Science.gov (United States)

Seftor, C. J.; Krotkov, N. A.; McPeters, R. D.; Li, J. Y.; Brentzel, K. W.; Habib, S.; Hassinen, S.; Heinrichs, T. A.; Schneider, D. J.

2014-12-01

NASA's Suomi NPP Ozone Science Team, in conjunction with Goddard Space Flight Center's (GSFC's) Direct Readout Laboratory, developed the capability of processing, in real-time, direct readout (DR) data from the Ozone Mapping and Profiler Suite (OMPS) to perform SO2 and Aerosol Index (AI) retrievals. The ability to retrieve this information from real-time processing of DR data was originally developed for the Ozone Monitoring Instrument (OMI) onboard the Aura spacecraft and is used by Volcano Observatories and Volcanic Ash Advisory Centers (VAACs) charged with mapping ash clouds from volcanic eruptions and providing predictions/forecasts about where the ash will go. The resulting real-time SO2 and AI products help to mitigate the effects of eruptions such as the ones from Eyjafjallajokull in Iceland and Puyehue-Cordón Caulle in Chile, which cause massive disruptions to airline flight routes for weeks as airlines struggle to avoid ash clouds that could cause engine failure, deeply pitted windshields impossible to see through, and other catastrophic events. We will discuss the implementation of real-time processing of OMPS DR data by both the Geographic Information Network of Alaska (GINA) and the Finnish Meteorological Institute (FMI), which provide real-time coverage over some of the most congested airspace and over many of the most active volcanoes in the world, and show examples of OMPS DR processing results from recent volcanic eruptions.

Residentś risk perception of and response to SO2 risk in east Iceland during the volcanic eruption in Bárðarbunga/Holuhraun 2014-2015

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Gísladóttir, Guðrún; Jóhannesdóttir, Guðrún

2016-04-01

Many Icelandic communities are exposed to volcanic eruptions every two to three years. In order to reduce risk and enhance resilience in communities exposed to volcanic hazards, involvement of local communities is essential during all phases of disaster management, from prevention and preparedness, to response and recovery. Preparedness plans for volcanic eruptions are in place for many of the volcanic hazards in Iceland especially evacuation of residents due to immediate threat from glacial outburst floods from sub-glacial eruptions. Some of the recent risks associated with volcanic eruptions have had a slow onset (volcanic gas) while others have had a sudden onset (volcanic ash). The risks are both linked to air quality in inhabited areas and dispersal are highly dependent on prevailing winds so timely forecast and modelling is needed in order to inform the population about the risk. Without preparedness plans many communities in Iceland were exposed to an unanticipated volcanic gas risks from Sulphur Dioxide (SO2) in 2014-2015 during an eruption in Bárðarbunga/Holuhraun. With no system in place to measure the highly toxic gas from the eruption, the Environmental Agency, The Department of Civil Protection and Emergency Management and the Directorate of Health set up a system with over 40 handheld gas detectors and online links to 7 detectors around Iceland to monitor the gas. The defined health limit of SO2 is 350 μg/m3 for one hour, while 2600 μg/m3 for 15 minutes for working outdoors. Nevertheless, some communities in Iceland experienced much higher values and the highest measured concentration in communities during the eruption was 21.000 μg/m3. When the concentration of SO2 reached the level of >1000 μg/m3 a warning was issued and SMS text messages were sent to all mobile phones in the affected area. In order to engage with residents during the eruption the Civil Protection and local authorities, Directorate of Health, scientist and specialists

First volcanic CO2 budget estimate for three actively degassing volcanoes in the Central American Volcanic Arc

Science.gov (United States)

Robidoux, Philippe; Aiuppa, Alessandro; Conde, Vladimir; Galle, Bo; Giudice, Gaetano; Avard, Geoffroy; Muñoz, Angélica

2014-05-01

CO2 is a key chemical tracer for exploring volcanic degassing mechanisms of basaltic magmatic systems (1). The rate of CO2 release from sub-aerial volcanism is monitored via studies on volcanic plumes and fumaroles, but information is still sparse and incomplete for many regions of the globe, including the majority of the volcanoes in the Central American Volcanic Arc (2). Here, we use a combination of remote sensing techniques and in-situ measurements of volcanic gas plumes to provide a first estimate of the CO2 output from three degassing volcanoes in Central America: Turrialba, in Costa Rica, and Telica and San Cristobal, in Nicaragua. During a field campaign in March-April 2013, we obtained (for the three volcanoes) a simultaneous record of SO2 fluxes (from the NOVAC network (3)) and CO2 vs. SO2 concentrations in the near-vent plumes (obtained via a temporary installed fully-automated Multi-GAS instrument (4)). The Multi-GAS time-series allowed to calculate the plume CO2/SO2 ratios for different intervals of time, showing relatively stable gas compositions. Distinct CO2 - SO2 - H2O proportions were observed at the three volcanoes, but still within the range of volcanic arc gas (5). The CO2/SO2 ratios were then multiplied by the SO2 flux in order to derive the CO2 output. At Turrialba, CO2/SO2 ratios fluctuated, between March 12 and 19, between 1.1 and 5.7, and the CO2flux was evaluated at ~1000-1350 t/d (6). At Telica, between March 23 and April 8, a somewhat higher CO2/SO2 ratio was observed (3.3 ± 1.0), although the CO2 flux was evaluated at only ~100-500 t/d (6). At San Cristobal, where observations were taken between April 11 and 15, the CO2/SO2 ratio ranged between 1.8 and 7.4, with a mean CO2 flux of 753 t/d. These measurements contribute refining the current estimates of the total CO2 output from the Central American Volcanic Arc (7). Symonds, R.B. et al., (2001). J. Volcanol. Geotherm. Res., 108, 303-341 Burton, M. R. et al. (2013). Reviews in

Atmospheric processes affecting the separation of volcanic ash and SO2 in volcanic eruptions: inferences from the May 2011 Grímsvötn eruption

Science.gov (United States)

Prata, Fred; Woodhouse, Mark; Huppert, Herbert E.; Prata, Andrew; Thordarson, Thor; Carn, Simon

2017-09-01

The separation of volcanic ash and sulfur dioxide (SO2) gas is sometimes observed during volcanic eruptions. The exact conditions under which separation occurs are not fully understood but the phenomenon is of importance because of the effects volcanic emissions have on aviation, on the environment, and on the earth's radiation balance. The eruption of Grímsvötn, a subglacial volcano under the Vatnajökull glacier in Iceland during 21-28 May 2011 produced one of the most spectacular examples of ash and SO2 separation, which led to errors in the forecasting of ash in the atmosphere over northern Europe. Satellite data from several sources coupled with meteorological wind data and photographic evidence suggest that the eruption column was unable to sustain itself, resulting in a large deposition of ash, which left a low-level ash-rich atmospheric plume moving southwards and then eastwards towards the southern Scandinavian coast and a high-level predominantly SO2 plume travelling northwards and then spreading eastwards and westwards. Here we provide observational and modelling perspectives on the separation of ash and SO2 and present quantitative estimates of the masses of ash and SO2 that erupted, the directions of transport, and the likely impacts. We hypothesise that a partial column collapse or sloughing fed with ash from pyroclastic density currents (PDCs) occurred during the early stage of the eruption, leading to an ash-laden gravity intrusion that was swept southwards, separated from the main column. Our model suggests that water-mediated aggregation caused enhanced ash removal because of the plentiful supply of source water from melted glacial ice and from entrained atmospheric water. The analysis also suggests that ash and SO2 should be treated with separate source terms, leading to improvements in forecasting the movement of both types of emissions.

The operational eEMEP model version 10.4 for volcanic SO2 and ash forecasting

Science.gov (United States)

Steensen, Birthe M.; Schulz, Michael; Wind, Peter; Valdebenito, Álvaro M.; Fagerli, Hilde

2017-05-01

This paper presents a new version of the EMEP MSC-W model called eEMEP developed for transportation and dispersion of volcanic emissions, both gases and ash. EMEP MSC-W is usually applied to study problems with air pollution and aerosol transport and requires some adaptation to treat volcanic eruption sources and effluent dispersion. The operational set-up of model simulations in case of a volcanic eruption is described. Important choices have to be made to achieve CPU efficiency so that emergency situations can be tackled in time, answering relevant questions of ash advisory authorities. An efficient model needs to balance the complexity of the model and resolution. We have investigated here a meteorological uncertainty component of the volcanic cloud forecast by using a consistent ensemble meteorological dataset (GLAMEPS forecast) at three resolutions for the case of SO2 emissions from the 2014 Barðarbunga eruption. The low resolution (40 × 40 km) ensemble members show larger agreement in plume position and intensity, suggesting that the ensemble here does not give much added value. To compare the dispersion at different resolutions, we compute the area where the column load of the volcanic tracer, here SO2, is above a certain threshold, varied for testing purposes between 0.25 and 50 Dobson units. The increased numerical diffusion causes a larger area (+34 %) to be covered by the volcanic tracer in the low resolution simulations than in the high resolution ones. The higher resolution (10 × 10 km) ensemble members show higher column loads farther away from the volcanic eruption site in narrower clouds. Cloud positions are more varied between the high resolution members, and the cloud forms resemble the observed clouds more than the low resolution ones. For a volcanic emergency case this means that to obtain quickly results of the transport of volcanic emissions, an individual simulation with our low resolution is sufficient; however, to forecast peak

Gas measurements from the Costa Rica-Nicaragua volcanic segment suggest possible along-arc variations in volcanic gas chemistry

Science.gov (United States)

Aiuppa, A.; Robidoux, P.; Tamburello, G.; Conde, V.; Galle, B.; Avard, G.; Bagnato, E.; De Moor, J. M.; Martínez, M.; Muñóz, A.

2014-12-01

Obtaining accurate estimates of the CO2 output from arc volcanism requires a precise understanding of the potential along-arc variations in volcanic gas chemistry, and ultimately of the magmatic gas signature of each individual arc segment. In an attempt to more fully constrain the magmatic gas signature of the Central America Volcanic Arc (CAVA), we present here the results of a volcanic gas survey performed during March and April 2013 at five degassing volcanoes within the Costa Rica-Nicaragua volcanic segment (CNVS). Observations of the volcanic gas plume made with a multicomponent gas analyzer system (Multi-GAS) have allowed characterization of the CO2/SO2-ratio signature of the plumes at Poás (0.30±0.06, mean ± SD), Rincón de la Vieja (27.0±15.3), and Turrialba (2.2±0.8) in Costa Rica, and at Telica (3.0±0.9) and San Cristóbal (4.2±1.3) in Nicaragua (all ratios on molar basis). By scaling these plume compositions to simultaneously measured SO2 fluxes, we estimate that the CO2 outputs at CNVS volcanoes range from low (25.5±11.0 tons/day at Poás) to moderate (918 to 1270 tons/day at Turrialba). These results add a new information to the still fragmentary volcanic CO2 output data set, and allow estimating the total CO2 output from the CNVS at 2835±1364 tons/day. Our novel results, with previously available information about gas emissions in Central America, are suggestive of distinct volcanic gas CO2/ST (= SO2 + H2S)-ratio signature for magmatic volatiles in Nicaragua (∼3) relative to Costa Rica (∼0.5-1.0). We also provide additional evidence for the earlier theory relating the CO2-richer signature of Nicaragua volcanism to increased contributions from slab-derived fluids, relative to more-MORB-like volcanism in Costa Rica. The sizeable along-arc variations in magmatic gas chemistry that the present study has suggested indicate that additional gas observations are urgently needed to more-precisely confine the volcanic CO2 from the CAVA, and from

Atmospheric processes affecting the separation of volcanic ash and SO2 in volcanic eruptions: inferences from the May 2011 Grímsvötn eruption

Directory of Open Access Journals (Sweden)

F. Prata

2017-09-01

Full Text Available The separation of volcanic ash and sulfur dioxide (SO2 gas is sometimes observed during volcanic eruptions. The exact conditions under which separation occurs are not fully understood but the phenomenon is of importance because of the effects volcanic emissions have on aviation, on the environment, and on the earth's radiation balance. The eruption of Grímsvötn, a subglacial volcano under the Vatnajökull glacier in Iceland during 21–28 May 2011 produced one of the most spectacular examples of ash and SO2 separation, which led to errors in the forecasting of ash in the atmosphere over northern Europe. Satellite data from several sources coupled with meteorological wind data and photographic evidence suggest that the eruption column was unable to sustain itself, resulting in a large deposition of ash, which left a low-level ash-rich atmospheric plume moving southwards and then eastwards towards the southern Scandinavian coast and a high-level predominantly SO2 plume travelling northwards and then spreading eastwards and westwards. Here we provide observational and modelling perspectives on the separation of ash and SO2 and present quantitative estimates of the masses of ash and SO2 that erupted, the directions of transport, and the likely impacts. We hypothesise that a partial column collapse or sloughing fed with ash from pyroclastic density currents (PDCs occurred during the early stage of the eruption, leading to an ash-laden gravity intrusion that was swept southwards, separated from the main column. Our model suggests that water-mediated aggregation caused enhanced ash removal because of the plentiful supply of source water from melted glacial ice and from entrained atmospheric water. The analysis also suggests that ash and SO2 should be treated with separate source terms, leading to improvements in forecasting the movement of both types of emissions.

Anthropogenic and volcanic emission impacts on SO2 dynamics and acid rain profiles. Numerical study using WRF-Chem in a high-resolution modeling

Science.gov (United States)

Vela, A. V.; González, C. M.; Ynoue, R.; Rojas, N. Y.; Aristizábal, B. H.; Wahl, M.

2017-12-01

Eulerian 3-D chemistry transport models (CTM) have been widely used for the study of air quality in urban environments, becoming an essential tool for studying the impacts and dynamics of gases and aerosols on air quality. However, their use in Colombia is scarce, especially in medium-sized cities, which are experimenting a fast urban growth, increasing the risk associated with possible air pollution episodes. In the densely populated medium-sized Andean city of Manizales, Colombia - a city located on the western slopes of the central range of the Andes (urban population 368000; 2150 m.a.s.l), there is an influence of the active Nevado del Ruiz volcano, located 28 km to the southwest. This natural source emits daily gas and particle fluxes, which could influence the atmospheric chemistry of the city and neighboring towns. Hence, the zone presents a unique combination of anthropogenic and volcanic sulfur gas emissions, which affects SO2 dynamics in the urban area, influencing also in the formation of acid rain phenomenon in the city. Therefore, studies analyzing the relative contribution of anthropogenic and volcanic emission could contribute with a deep understanding about causes and dynamics of both acid rain phenomenon and ambient SO2 levels in Manizales. This work aimed to analyze the influence of anthropogenic (on-road vehicular and industrial point-sources) and volcanic sulfur emissions in SO2 atmospheric chemistry dynamics, evaluating its possible effects on acid rain profiles. Ambient SO2 levels and day-night rain samples were measured and used to analyze results obtained from the application of the fully-coupled on-line WRF-Chem model. Two high-resolution simulations were performed during two dry and wet one-week periods in 2015. Analysis of SO2 dispersion patterns and comparison with SO2 observations in the urban area were performed for three different scenarios in which natural and anthropogenic emissions were simulated separately. Results suggest that

SO2 EMISSION MEASUREMENT BY DOAS (DIFFERENTIAL OPTICAL ABSORPTION SPECTROSCOPY AND COSPEC (CORRELATION SPECTROSCOPY AT MERAPI VOLCANO (INDONESIA

Directory of Open Access Journals (Sweden)

Hanik Humaida

2010-06-01

Full Text Available The SO2 is one of the volcanic gases that can use as indicator of volcano activity. Commonly, SO2 emission is measured by COSPEC (Correlation Spectroscopy. This equipment has several disadvantages; such as heavy, big in size, difficulty in finding spare part, and expensive. DOAS (Differential Optical Absorption Spectroscopy is a new method for SO2 emission measurement that has advantages compares to the COSPEC. Recently, this method has been developed. The SO2 gas emission measurement of Gunung Merapi by DOAS has been carried out at Kaliadem, and also by COSPEC method as comparation. The differences of the measurement result of both methods are not significant. However, the differences of minimum and maximum result of DOAS method are smaller than that of the COSPEC. It has range between 51 ton/day and 87 ton/day for DOAS and 87 ton/day and 201 ton/day for COSPEC. The measurement of SO2 gas emission evaluated with the seismicity data especially the rockfall showed the presence of the positive correlation. It may cause the gas pressure in the subsurface influencing instability of 2006 eruption lava.   Keywords: SO2 gas, Merapi, DOAS, COSPEC

Estimation of the rate of volcanism on Venus from reaction rate measurements

Science.gov (United States)

Fegley, Bruce, Jr.; Prinn, Ronald G.

1989-01-01

Laboratory rate data for the reaction between SO2 and calcite to form anhydrite are presented. If this reaction rate represents the SO2 reaction rate on Venus, then all SO2 in the Venusian atmosphere will disappear in 1.9 Myr unless volcanism replenishes the lost SO2. The required volcanism rate, which depends on the sulfur content of the erupted material, is in the range 0.4-11 cu km of magma erupted per year. The Venus surface composition at the Venera 13, 14, and Vega 2 landing sites implies a volcanism rate of about 1 cu km/yr. This geochemically estimated rate can be used to determine if either (or neither) of two discordant geophysically estimated rates is correct. It also suggests that Venus may be less volcanically active than the earth.

Intercomparison of Metop-A SO2 measure- ments during the 2010- 2011 Icelandic eruptions

Directory of Open Access Journals (Sweden)

Maria Elissavet Koukouli

2015-03-01

Full Text Available The European Space Agency project Satellite Monitoring of Ash and Sulphur Dioxide for the mitigation of Avi­ ation Hazards, was introduced after the eruption of the Icelandic volcano Eyjafjallajökull in the spring of 2010 to facilitate the development of an optimal End­to­End System for Volcanic Ash Plume Monitoring and Predic­ tion. The Eyjafjallajökull plume drifted towards Europe and caused major disruptions of European air traffic for several weeks affecting the everyday life of millions of people. The limitations in volcanic plume monitoring and prediction capabilities gave birth to this observational system which is based on comprehensive satellite­derived ash plume and sulphur dioxide [SO2] level estimates, as well as a widespread validation using supplementary satellite, aircraft and ground­based measurements. Inter­comparison of the volcanic total SO2 column and plume height observed by GOME­2/Metop­A and IASI/Metop­A are shown before, during and after the Eyjaf­ jallajökull 2010 eruptions as well as for the 2011 Grímsvötn eruption. Co­located ground­based Brewer Spectro­ photometer data extracted from the World Ozone and Ultraviolet Radiation Data Centre for de Bilt, the Nether­ lands, are also compared to the different satellite estimates. Promising agreement is found for the two different types of instrument for the SO2 columns with linear regression coefficients ranging around from 0.64 when comparing the different instruments and 0.85 when comparing the two different IASI algorithms. The agree­ ment for the plume height is lower, possibly due to the major differences between the height retrieval part of the GOME2 and IASI algorithms. The comparisons with the Brewer ground­based station in de Bilt, The Nether­ lands show good qualitative agreement for the peak of the event however stronger eruptive signals are required for a longer quantitative comparison. 

New-Generation NASA Aura Ozone Monitoring Instrument (OMI) Volcanic SO2 Dataset: Algorithm Description, Initial Results, and Continuation with the Suomi-NPP Ozone Mapping and Profiler Suite (OMPS)

Science.gov (United States)

Li, Can; Krotkov, Nickolay A.; Carn, Simon; Zhang, Yan; Spurr, Robert J. D.; Joiner, Joanna

2017-01-01

Since the fall of 2004, the Ozone Monitoring Instrument (OMI) has been providing global monitoring of volcanic SO2 emissions, helping to understand their climate impacts and to mitigate aviation hazards. Here we introduce a new-generation OMI volcanic SO2 dataset based on a principal component analysis (PCA) retrieval technique. To reduce retrieval noise and artifacts as seen in the current operational linear fit (LF) algorithm, the new algorithm, OMSO2VOLCANO, uses characteristic features extracted directly from OMI radiances in the spectral fitting, thereby helping to minimize interferences from various geophysical processes (e.g., O3 absorption) and measurement details (e.g., wavelength shift). To solve the problem of low bias for large SO2 total columns in the LF product, the OMSO2VOLCANO algorithm employs a table lookup approach to estimate SO2 Jacobians (i.e., the instrument sensitivity to a perturbation in the SO2 column amount) and iteratively adjusts the spectral fitting window to exclude shorter wavelengths where the SO2 absorption signals are saturated. To first order, the effects of clouds and aerosols are accounted for using a simple Lambertian equivalent reflectivity approach. As with the LF algorithm, OMSO2VOLCANO provides total column retrievals based on a set of predefined SO2 profiles from the lower troposphere to the lower stratosphere, including a new profile peaked at 13 km for plumes in the upper troposphere. Examples given in this study indicate that the new dataset shows significant improvement over the LF product, with at least 50% reduction in retrieval noise over the remote Pacific. For large eruptions such as Kasatochi in 2008 (approximately 1700 kt total SO2/ and Sierra Negra in 2005 (greater than 1100DU maximum SO2), OMSO2VOLCANO generally agrees well with other algorithms that also utilize the full spectral content of satellite measurements, while the LF algorithm tends to underestimate SO2. We also demonstrate that, despite the

Simulations of the Holuhraun eruption 2014 with WRF-Chem and evaluation with satellite and ground based SO2 measurements

Science.gov (United States)

Hirtl, Marcus; Arnold-Arias, Delia; Flandorfer, Claudia; Maurer, Christian; Mantovani, Simone; Natali, Stefano

2016-04-01

Volcanic eruptions, with gas or/and particle emissions, directly influence our environment, with special significance when they either occur near inhabited regions or are transported towards them. In addition to the well-known affectation of air traffic, with large economic impacts, the ground touching plumes can lead directly to an influence of soil, water and even to a decrease of air quality. The eruption of Holuhraun in August 2014 in central Iceland is the country's largest lava and gas eruption since the Lakagígar eruption in 1783. Nevertheless, very little volcanic ash was produced. The main atmospheric threat from this event was the SO2 pollution that frequently violated the Icelandic National Air Quality Standards in many population centers. However, the SO2 affectation was not limited to Iceland but extended to mainland Europe. The on-line coupled model WRF-Chem is used to simulate the dispersion of SO2 for this event that affected the central European regions. The volcanic emissions are considered in addition to the anthropogenic and biogenic ground sources at European scale. A modified version of WRF-Chem version 4.1 is used in order to use time depending injection heights and mass fluxes which were obtained from in situ observations. WRF-Chem uses complex gas- (RADM2) and aerosol- (MADE-SORGAM) chemistry and is operated on a European domain (12 km resolution), and a nested grid covering the Alpine region (4 km resolution). The study is showing the evaluation of the model simulations with satellite and ground based measurement data of SO2. The analysis is conducted on a data management platform, which is currently developed in the frame of the ESA-funded project TAMP "Technology and Atmospheric Mission Platform": it provides comprehensive functionalities to visualize and numerically compare data from different sources (model, satellite and ground-measurements).

Using Volcanic Lightning Measurements to Discern Variations in Explosive Volcanic Activity

Science.gov (United States)

Behnke, S. A.; Thomas, R. J.; McNutt, S. R.; Edens, H. E.; Krehbiel, P. R.; Rison, W.

2013-12-01

VHF observations of volcanic lightning have been made during the recent eruptions of Augustine Volcano (2006, Alaska, USA), Redoubt Volcano (2009, Alaska, USA), and Eyjafjallajökull (2010, Iceland). These show that electrical activity occurs both on small scales at the vent of the volcano, concurrent with an eruptive event and on large scales throughout the eruption column during and subsequent to an eruptive event. The small-scale discharges at the vent of the volcano are often referred to as 'vent discharges' and are on the order of 10-100 meters in length and occur at rates on the order of 1000 per second. The high rate of vent discharges produces a distinct VHF signature that is sometimes referred to as 'continuous RF' radiation. VHF radiation from vent discharges has been observed at sensors placed as far as 100 km from the volcano. VHF and infrasound measurements have shown that vent discharges occur simultaneously with the onset of eruption, making their detection an unambiguous indicator of explosive volcanic activity. The fact that vent discharges are observed concurrent with explosive volcanic activity indicates that volcanic ejecta are charged upon eruption. VHF observations have shown that the intensity of vent discharges varies between eruptive events, suggesting that fluctuations in eruptive processes affect the electrification processes giving rise to vent discharges. These fluctuations may be variations in eruptive vigor or variations in the type of eruption; however, the data obtained so far do not show a clear relationship between eruption parameters and the intensity or occurrence of vent discharges. Further study is needed to clarify the link between vent discharges and eruptive behavior, such as more detailed lightning observations concurrent with tephra measurements and other measures of eruptive strength. Observations of vent discharges, and volcanic lightning observations in general, are a valuable tool for volcano monitoring, providing a

Dynamics and Evolution of SO 2 Gas Condensation around Prometheus-like Volcanic Plumes on Io as Seen by the Near Infrared Mapping Spectrometer

Science.gov (United States)

Douté, Sylvain; Lopes, Rosaly; Kamp, Lucas W.; Carlson, Robert; Schmitt, Bernard; Galileo NIMS Team

2002-08-01

We analyze a series of spectral image cubes acquired by the Galileo Near Infrared Mapping Spectrometer (NIMS) over the Prometheus region of Io. We use SO 2 frost, a volatile compound ubiquitous on the surface, as a tracer to understand various thermodynamic and volcanic processes acting in this equatorial region. Here we develop a new method to derive, from the 12-wavelength NIMS products, the distribution and physical properties of solid SO 2. This method is based on the inversion of a bidirectional reflectance model on two observed spectral ratios sensitive to (1) the areal abundance of SO 2 and (2) its mean grain size. As a result, reliable and consistent maps of SO 2 abundance and granularity are obtained which can be correlated to distinguish four different physical units. The distribution of these SO 2 units indicates zones of condensation, metamorphism, and sublimation linked with the thermodynamic and volcanic processes of interest. Our maps depict equatorial plains undisturbed by any kind of vigorous volcanic activity over 35-40% of their surface. Elsewhere, 10-20% of the equatorial plains display abnormally low frost coverage which may imply the recent presence of positive thermal anomalies with temperatures in the range 110-200 K. Hot-spots such as Prometheus, Culann, Surya, and Tupan (to mention the most persistent) emit a great variety of gases, some of which will condense at Io's surface near their source regions. Associated fields of freshly condensed SO 2 are easily observed, and deposits of more refractory compounds with higher (e.g., S 8) or lower (e.g., NaCl) molecular weight must also be present (although their exact nature is unknown). Three different mechanisms of emission are proposed for the volatile compounds and supported by the distribution maps. These are (a) the interaction between flowing lava and preexisting volatile deposits on the surface, (b) direct degassing from the lava, an d (c) the eruption of a liquid aquifer from underground

Rate of volcanism on Venus

International Nuclear Information System (INIS)

Fegley, B. Jr.; Prinn, R.G.

1988-07-01

The maintenance of the global H 2 SO 4 clouds on Venus requires volcanism to replenish the atmospheric SO 2 which is continually being removed from the atmosphere by reaction with calcium minerals on the surface of Venus. The first laboratory measurements of the rate of one such reaction, between SO 2 and calcite (CaCO 3 ) to form anhydrite (CaSO 4 ), are reported. If the rate of this reaction is representative of the SO 2 reaction rate at the Venus surface, then we estimate that all SO 2 in the Venus atmosphere (and thus the H 2 SO 4 clouds) will be removed in 1.9 million years unless the lost SO 2 is replenished by volcanism. The required rate of volcanism ranges from about 0.4 to about 11 cu km of magma erupted per year, depending on the assumed sulfur content of the erupted material. If this material has the same composition as the Venus surface at the Venera 13, 14 and Vega 2 landing sites, then the required rate of volcanism is about 1 cu km per year. This independent geochemically estimated rate can be used to determine if either (or neither) of the two discordant (2 cu km/year vs. 200 to 300 cu km/year) geophysically estimated rates is correct. The geochemically estimated rate also suggests that Venus is less volcanically active than the Earth

Atmospheric SO{sub 2}. Global measurements using aircraft-based CIMS

Energy Technology Data Exchange (ETDEWEB)

Fiedler, V.

2008-06-27

Aircraft based measurements of tropospheric sulfur dioxide, SO{sub 2}, have been carried out during four campaigns in South America (TROCCINOX), Australia (SCOUT-O3), Europe (INTEX/MEGAPLUME) and Africa (AMMA). SO{sub 2} has been measured by chemical ionization mass spectrometry (CIMS), permanently online calibrated with isotopically labelled SO{sub 2}. The measurement method is described thoroughly in this work and the measured data are presented. Moreover, the data of the different regions are compared in general and typical air mass situations with SO{sub 2} enhancement are shown. A detailed analysis of four SO{sub 2} pollution plume cases emphasizes the main features: long-range transport, SO{sub 2} from metal smelters/volcanoes or from biomass burning. The SO{sub 2} measurements are analyzed in the light of simultaneously measured trace gas, particle and meteorological data. Air mass trajectory models (FLEXPART or HYSPLIT) are employed for a determination of the pollution origin. Further going evaluations with the aerosol model AEROFOR complete the analyses and point out, that the measured SO{sub 2} mole fractions are sufficient to explain new particle formation and growth. Finally, a first comparison of the measured SO{sub 2} to results from a global circulation model (ECHAM) with implemented sulfur chemistry showed a significant underestimation of the measured SO{sub 2} mole fraction by the model in the free troposphere. (orig.)

Implementation of electrochemical, optical and denuder-based sensors and sampling techniques on UAV for volcanic gas measurements: examples from Masaya, Turrialba and Stromboli volcanoes

Science.gov (United States)

Rüdiger, Julian; Tirpitz, Jan-Lukas; Maarten de Moor, J.; Bobrowski, Nicole; Gutmann, Alexandra; Liuzzo, Marco; Ibarra, Martha; Hoffmann, Thorsten

2018-04-01

Volcanoes are a natural source of several reactive gases (e.g., sulfur and halogen containing species) and nonreactive gases (e.g., carbon dioxide) to the atmosphere. The relative abundance of carbon and sulfur in volcanic gas as well as the total sulfur dioxide emission rate from a volcanic vent are established parameters in current volcano-monitoring strategies, and they oftentimes allow insights into subsurface processes. However, chemical reactions involving halogens are thought to have local to regional impact on the atmospheric chemistry around passively degassing volcanoes. In this study we demonstrate the successful deployment of a multirotor UAV (quadcopter) system with custom-made lightweight payloads for the compositional analysis and gas flux estimation of volcanic plumes. The various applications and their potential are presented and discussed in example studies at three volcanoes encompassing flight heights of 450 to 3300 m and various states of volcanic activity. Field applications were performed at Stromboli volcano (Italy), Turrialba volcano (Costa Rica) and Masaya volcano (Nicaragua). Two in situ gas-measuring systems adapted for autonomous airborne measurements, based on electrochemical and optical detection principles, as well as an airborne sampling unit, are introduced. We show volcanic gas composition results including abundances of CO2, SO2 and halogen species. The new instrumental setups were compared with established instruments during ground-based measurements at Masaya volcano, which resulted in CO2 / SO2 ratios of 3.6 ± 0.4. For total SO2 flux estimations a small differential optical absorption spectroscopy (DOAS) system measured SO2 column amounts on transversal flights below the plume at Turrialba volcano, giving 1776 ± 1108 T d-1 and 1616 ± 1007 T d-1 of SO2 during two traverses. At Stromboli volcano, elevated CO2 / SO2 ratios were observed at spatial and temporal proximity to explosions by airborne in situ measurements. Reactive

Volcanic gas emissions and degassing dynamics at Ubinas and Sabancaya volcanoes; implications for the volatile budget of the central volcanic zone

Science.gov (United States)

Moussallam, Yves; Tamburello, Giancarlo; Peters, Nial; Apaza, Fredy; Schipper, C. Ian; Curtis, Aaron; Aiuppa, Alessandro; Masias, Pablo; Boichu, Marie; Bauduin, Sophie; Barnie, Talfan; Bani, Philipson; Giudice, Gaetano; Moussallam, Manuel

2017-09-01

Emission of volcanic gas is thought to be the dominant process by which volatiles transit from the deep earth to the atmosphere. Volcanic gas emissions, remain poorly constrained, and volcanoes of Peru are entirely absent from the current global dataset. In Peru, Sabancaya and Ubinas volcanoes are by far the largest sources of volcanic gas. Here, we report the first measurements of the compositions and fluxes of volcanic gases emitted from these volcanoes. The measurements were acquired in November 2015. We determined an average SO2 flux of 15.3 ± 2.3 kg s- 1 (1325-ton day- 1) at Sabancaya and of 11.4 ± 3.9 kg s- 1 (988-ton day- 1) at Ubinas using scanning ultraviolet spectroscopy and dual UV camera systems. In-situ Multi-GAS analyses yield molar proportions of H2O, CO2, SO2, H2S and H2 gases of 73, 15, 10 1.15 and 0.15 mol% at Sabancaya and of 96, 2.2, 1.2 and 0.05 mol% for H2O, CO2, SO2 and H2S at Ubinas. Together, these data imply cumulative fluxes for both volcanoes of 282, 30, 27, 1.2 and 0.01 kg s- 1 of H2O, CO2, SO2, H2S and H2 respectively. Sabancaya and Ubinas volcanoes together contribute about 60% of the total CO2 emissions from the Central Volcanic zone, and dominate by far the total revised volatile budget of the entire Central Volcanic Zone of the Andes.

Time Series of SO2 Flux from Popocatépetl Volcano by an Ultra-Violet Camera with a Set of Different Band-Pass Filters

Science.gov (United States)

Schiavo, B.; Stremme, W.; Grutter, M.; Campion, R.; Rivera, C. I.; Inguaggiato, S.

2017-12-01

The measurement of SO2flux from active volcanoes are of great importance, for monitoring and hazard of volcanic activity, environmental impact and flux emissions related to changes of magmatic activity. Sulfur dioxide total flux from Popocatépetl volcano was determinad using a ultra-violet camera (or SO2 camera) with different band-pass filter. The flux is obteined from the product of the gas concentration over integrated the plume cross-section (slant column in molec/cm2 or ppm*m) and wind velocity data. Model of plume altitude and wind speed measurement are used to calculate a wind velocity, but a new method of sequential images is widely used in several years for this calculation. Volcanic plume measurements, for a total of about 60 days from from January to March 2017, were collected and utilized to generate the SO2 time series. The importance of monitoring and the time series of volcanic gas emissions is described and proven by many scientific studies. A time series of the Popocatépetl volcano will allow us to detect the volcanic gas as well as anomalies in volcanic processes and help to estimate the average SO2 flux of the volcano. We present a detailed description of the posterior correction of the dilution effect, which occurs due to a simplification of the radiative transfer equation. The correction scheme is especial applicable for long term monitoring from a permanent observation site. Images of volcanic SO2 plumes from the active Popocatépetl volcano in Mexico are presented, showing persistent passive degassing. The measurment are taken from the Altzomoni Atmospheric Observatory (19.12N, -98.65W, 3,985 m.a.s.l.), which forms part of the RUOA (www.ruoa.unam.mx) and NDACC (https://www2.acom.ucar.edu/irwg) networks. It is located north of the crater at 11 km distance. The data to calculate SO2 flux (t/d or kg/s) were recorded with the QSI UV camera and processed using Python scripts.

Characterizing Volcanic Eruptions on Venus: Some Realistic (?) Scenarios

Science.gov (United States)

Stofan, E. R.; Glaze, L. S.; Grinspoon, D. H.

2011-01-01

When Pioneer Venus arrived at Venus in 1978, it detected anomalously high concentrations of SO2 at the top of the troposphere, which subsequently declined over the next five years. This decline in SO2 was linked to some sort of dynamic process, possibly a volcanic eruption. Observations of SO2 variability have persisted since Pioneer Venus. More recently, scientists from the Venus Express mission announced that the SPICAV (Spectroscopy for Investigation of Characteristics of the Atmosphere of Venus) instrument had measured varying amounts of SO2 in the upper atmosphere; VIRTIS (Visible and Infrared Thermal Imaging Spectrometer) measured no similar variations in the lower atmosphere (ESA, 4 April, 2008). In addition, Fegley and Prinn stated that venusian volcanoes must replenish SO2 to the atmosphere, or it would react with calcite and disappear within 1.9 my. Fegley and Tremain suggested an eruption rate on the order of approx 1 cubic km/year to maintain atmospheric SO2; Bullock and Grinspoon posit that volcanism must have occurred within the last 20-50 my to maintain the sulfuric acid/water clouds on Venus. The abundance of volcanic deposits on Venus and the likely thermal history of the planet suggest that it is still geologically active, although at rates lower than Earth. Current estimates of resurfacing rates range from approx 0.01 cubic km/yr to approx 2 cubic km/yr. Demonstrating definitively that Venus is still volcanically active, and at what rate, would help to constrain models of evolution of the surface and interior, and help to focus future exploration of Venus.

Implementation of electrochemical, optical and denuder-based sensors and sampling techniques on UAV for volcanic gas measurements: examples from Masaya, Turrialba and Stromboli volcanoes

Directory of Open Access Journals (Sweden)

J. Rüdiger

2018-04-01

Full Text Available Volcanoes are a natural source of several reactive gases (e.g., sulfur and halogen containing species and nonreactive gases (e.g., carbon dioxide to the atmosphere. The relative abundance of carbon and sulfur in volcanic gas as well as the total sulfur dioxide emission rate from a volcanic vent are established parameters in current volcano-monitoring strategies, and they oftentimes allow insights into subsurface processes. However, chemical reactions involving halogens are thought to have local to regional impact on the atmospheric chemistry around passively degassing volcanoes. In this study we demonstrate the successful deployment of a multirotor UAV (quadcopter system with custom-made lightweight payloads for the compositional analysis and gas flux estimation of volcanic plumes. The various applications and their potential are presented and discussed in example studies at three volcanoes encompassing flight heights of 450 to 3300 m and various states of volcanic activity. Field applications were performed at Stromboli volcano (Italy, Turrialba volcano (Costa Rica and Masaya volcano (Nicaragua. Two in situ gas-measuring systems adapted for autonomous airborne measurements, based on electrochemical and optical detection principles, as well as an airborne sampling unit, are introduced. We show volcanic gas composition results including abundances of CO2, SO2 and halogen species. The new instrumental setups were compared with established instruments during ground-based measurements at Masaya volcano, which resulted in CO2 ∕ SO2 ratios of 3.6 ± 0.4. For total SO2 flux estimations a small differential optical absorption spectroscopy (DOAS system measured SO2 column amounts on transversal flights below the plume at Turrialba volcano, giving 1776 ± 1108 T d−1 and 1616 ± 1007 T d−1 of SO2 during two traverses. At Stromboli volcano, elevated CO2 ∕ SO2 ratios were observed at spatial and temporal proximity

The flight of Arcadia: spatial CO2/SO2 variations in a cross section above the Nord East crater of Etna volcano

Science.gov (United States)

Giuffrida, Giovanni; Calabrese, Sergio; Bobrowski, Nicole; Finkenzeller, Henning; Pecoraino, Giovannella; Scaglione, Sarah

2015-04-01

The CO2/SO2 ratio in volcanic plumes of open conduit volcanoes can provide useful information about the magma depth inside a conduit and the possible occurrence of an eruptive event. Moreover, the same CO2 measurement when combined with a SO2 flux measurement, commonly carried out at many volcanoes nowadays, is used to contribute to an improved estimate of global volcanic CO2 budget. Today worldwide at 13 volcanoes automated in-situ instruments (known as Multi-GAS stations) are applied to continuously determine CO2/SO2 ratios and to use this signal as additional parameter for volcanic monitoring. Usually these instruments carry out measurements of half an hour 4 - 6 times/day and thus provide continuous CO2/SO2 values and their variability. The stations are located at crater rims in a position that according to the prevailing winds is invested by the plume. Obviously, although the stations are carefully positioned, it is inevitable that other sources than the plume itself, e.g. soil degassing and surrounding fumaroles, contribute and will be measured as well, covering the 'real' values. Between July and September 2014 experiments were carried out on the North East crater (NEC) of Mount Etna, installing a self-made cable car that crossed the crater from one side to the other. The basket, called "Arcadia", was equipped with an automated standard Multi-GAS station and a GPS, which acquired at high frequency (0.5 Hz) the following parameters : CO2, SO2, H2S, Rh, T, P and geo-coordinates. The choice of NEC of the volcano Etna was based on its accessibility, the relative small diameter (about 230 m) and the presence of a relatively constant and rather concentrated plume. Actually, NEC belongs also to the monitoring network EtnaPlume (managed by the INGV of Palermo). The aim of these experiments was to observe variations of each parameter, in particular the fluctuation of the CO2/SO2 ratio within the plume, moving from the edge to the center of the crater. The gained

Monitoring so2 emission at the Soufriere Hills volcano: Implications for changes in eruptive conditions

Science.gov (United States)

Young, S.R.; Francis, P.W.; Barclay, J.; Casadevall, T.J.; Gardner, C.A.; Darroux, B.; Davies, M.A.; Delmelle, P.; Norton, G.E.; Maciejewski, A.J.H.; Oppenheimer, C.M.M.; Stix, J.; Watson, I.M.

1998-01-01

Correlation spectrometer measurements of sulfur dioxide (SO2) emission rates during the current eruption of the Soufriere Hills volcano, Montserrat, have contributed towards identifying different phases of volcanic activity. SO2 emission rate has increased from 550 td-1 (>6.4 kgs-1) after July 1996, with the uncertainty associated with any individual measurement ca. 30%. Significantly enhanced SO2 emission rates have been identified in association with early phreatic eruptions (800 td-1 (9.3 kgs-1)) and episodes of vigorous dome collapse and pyroclastic flow generation (900 to 1500 td-1 (10.4 to 17.4 kgs-1)). SO2 emission rate has proved a useful proxy measurement for magma production rate. Observed SO2 emission rates are significantly higher than those inferred from analyses of glass inclusions in phenocrysts, implying the existence of a S-rich magmatic vapour phase.

Emission of SO2, CO2, and H2S from Augustine Volcano, 2002-2008: Chapter 26 in The 2006 eruption of Augustine Volcano, Alaska

Science.gov (United States)

McGee, Kenneth A.; Doukas, Michael P.; McGimsey, Robert G.; Neal, Christina A.; Wessels, Rick L.; Power, John A.; Coombs, Michelle L.; Freymueller, Jeffrey T.

2010-01-01

Airborne surveillance of gas emissions from Augustine Volcano and other Cook Inlet volcanoes began in 1990 to identify baseline emission levels during noneruptive conditions. Gas measurements at Augustine for SO2, CO2, and H2S showed essentially no evidence of anomalous degassing through spring 2005. Neither did a measurement on May 10, 2005, right after the onset of low level seismicity and inflation. The following measurement, on December 20, 2005, showed Augustine to be degassing about 600 metric tons per day (t/d) of SO2, and by January 4, 2006, only 7 days before the first explosive event, SO2 emissions had climbed to ten times that amount. Maximum emission rates measured during the subsequent eruption were: 8,930 t/d SO2 (February 24, 2006), 1,800 t/d CO2 (March 9, 2006), and 4.3 t/d H2S (January 19, 2006). In total, 45 measurements for SO2 were made from December 2005 through the end of 2008, with 19 each for CO2 and H2S during the same period. Molar CO2/SO2 ratios averaged about 1.6. In general, SO2 emissions appeared to increase during inflation of the volcanic edifice, whereas CO2 emissions were at their highest during the period of deflation associated with the vigorous effusive phase of the eruption in March. High SO2 was probably associated with degassing of shallow magma, whereas high CO2 likely reflected deep (>4 km) magma recharge of the sub-volcanic plumbing system, For the 2005–6 period, the volcano released a total of about 1.5×106 tons of CO2 to the atmosphere, a level similar to the annual output of a medium-sized natural-gas-fired powerplant. Augustine also emitted about 8×105 tons of SO2, similar to that produced by the 1976 and 1986 eruptions of the volcano.

The 2010 Eyja eruption evolution by using IR satellite sensors measurements: retrieval comparison and insights into explosive volcanic processes

Science.gov (United States)

Piscini, A.; Corradini, S.; Merucci, L.; Scollo, S.

2010-12-01

The 2010 April-May Eyja eruption caused an unprecedented disruption to economic, political and cultural activities in Europe and across the world. Because of the harming effects of fine ash particles on aircrafts, many European airports were in fact closed causing millions of passengers to be stranded, and with a worldwide airline industry loss estimated of about 2.5 billion Euros. Both security and economical issues require robust and affordable volcanic cloud retrievals that may be really improved through the intercomparison among different remote sensing instruments. In this work the Thermal InfraRed (TIR) measurements of different polar and geostationary satellites instruments as the Moderate Resolution Imaging Spectroradiometer (MODIS), the Advanced Very High Resolution Radiometer (AVHRR) and the Spin Enhanced Visible and Infrared Imager (SEVIRI), have been used to retrieve the volcanic ash and SO2 in the entire eruption period over Iceland. The ash retrievals (mass, AOD and effective radius) have been carried out by means of the split window BTD technique using the channels centered around 11 and 12 micron. The least square fit procedure is used for the SO2 retrieval by using the 7.3 and 8.7 micron channels. The simulated TOA radiance Look-Up Table (LUT) needed for both the ash and SO2 column abundance retrievals have been computed using the MODTRAN 4 Radiative Transfer Model. Further, the volcanic plume column altitude and ash density have been computed and compared, when available, with ground observations. The results coming from the retrieval of different IR sensors show a good agreement over the entire eruption period. The column height, the volcanic ash and the SO2 emission trend confirm the indentified different phases occurred during the Eyja eruption. We remark that the retrieved volcanic plume evolution can give important insights into eruptive dynamics during long-lived explosive activity.

Progress in Near Real-Time Volcanic Cloud Observations Using Satellite UV Instruments

Science.gov (United States)

Krotkov, N. A.; Yang, K.; Vicente, G.; Hughes, E. J.; Carn, S. A.; Krueger, A. J.

2011-12-01

Volcanic clouds from explosive eruptions can wreak havoc in many parts of the world, as exemplified by the 2010 eruption at the Eyjafjöll volcano in Iceland, which caused widespread disruption to air traffic and resulted in economic impacts across the globe. A suite of satellite-based systems offer the most effective means to monitor active volcanoes and to track the movement of volcanic clouds globally, providing critical information for aviation hazard mitigation. Satellite UV sensors, as part of this suite, have a long history of making unique near-real time (NRT) measurements of sulfur dioxide (SO2) and ash (aerosol Index) in volcanic clouds to supplement operational volcanic ash monitoring. Recently a NASA application project has shown that the use of near real-time (NRT,i.e., not older than 3 h) Aura/OMI satellite data produces a marked improvement in volcanic cloud detection using SO2 combined with Aerosol Index (AI) as a marker for ash. An operational online NRT OMI AI and SO2 image and data product distribution system was developed in collaboration with the NOAA Office of Satellite Data Processing and Distribution. Automated volcanic eruption alarms, and the production of volcanic cloud subsets for multiple regions are provided through the NOAA website. The data provide valuable information in support of the U.S. Federal Aviation Administration goal of a safe and efficient National Air Space. In this presentation, we will highlight the advantages of UV techniques and describe the advances in volcanic SO2 plume height estimation and enhanced volcanic ash detection using hyper-spectral UV measurements, illustrated with Aura/OMI observations of recent eruptions. We will share our plan to provide near-real-time volcanic cloud monitoring service using the Ozone Mapping and Profiler Suite (OMPS) on the Joint Polar Satellite System (JPSS).

Identification of tropospheric emissions sources from satellite observations: Synergistic use of HCHO, NO2, and SO2 trace gas measurements

Science.gov (United States)

Marbach, T.; Beirle, S.; Khokhar, F.; Platt, U.

2005-12-01

We present case studies for combined HCHO, NO2, and SO2 satellite observations, derived from GOME measurements. Launched on the ERS-2 satellite in April 1995, GOME has already performed continuous operations over 8 years providing global observations of the different trace gases. In this way, satellite observations provide unique opportunities for the identifications of trace gas sources. The satellite HCHO observations provide information concerning the localization of biomass burning (intense source of HCHO). The principal biomass burning areas can be observed in the Amazon basin region and in central Africa Weaker HCHO sources (south east of the United States, northern part of the Amazon basin, and over the African tropical forest), not correlated with biomass burning, could be due to biogenic isoprene emissions. The HCHO data can be compared with NO2 and SO2 results to identify more precisely the tropospheric sources (biomass burning events, human activities, additional sources like volcanic emissions). Biomass burning are important tropospheric sources for both HCHO and NO2. Nevertheless HCHO reflects more precisely the biomass burning as it appears in all biomass burning events. NO2 correlate with HCHO over Africa (grassland fires) but not over Indonesia (forest fires). In south America, an augmentation of the NO2 concentrations can be observed with the fire shift from the forest to grassland vegetation. So there seems to be a dependence between the NO2 emissions during biomass burning and the vegetation type. Other high HCHO, SO2, and NO2 emissions can be correlated with climatic events like the El Nino in 1997, which induced dry conditions in Indonesia causing many forest fires.

Ozone Depletion in Tropospheric Volcanic Plumes: From Halogen-Poor to Halogen-Rich Emissions

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Tjarda J. Roberts

2018-02-01

Full Text Available Volcanic halogen emissions to the troposphere undergo a rapid plume chemistry that destroys ozone. Quantifying the impact of volcanic halogens on tropospheric ozone is challenging, only a few observations exist. This study presents measurements of ozone in volcanic plumes from Kīlauea (HI, USA, a low halogen emitter. The results are combined with published data from high halogen emitters (Mt Etna, Italy; Mt Redoubt, AK, USA to identify controls on plume processes. Ozone was measured during periods of relatively sustained Kīlauea plume exposure, using an Aeroqual instrument deployed alongside Multi-Gas SO2 and H2S sensors. Interferences were accounted for in data post-processing. The volcanic H2S/SO2 molar ratio was quantified as 0.03. At Halema‘uma‘u crater-rim, ozone was close to ambient in the emission plume (at 10 ppmv SO2. Measurements in grounding plume (at 5 ppmv SO2 about 10 km downwind of Pu‘u ‘Ō‘ō showed just slight ozone depletion. These Kīlauea observations contrast with substantial ozone depletion reported at Mt Etna and Mt Redoubt. Analysis of the combined data from these three volcanoes identifies the emitted Br/S as a strong but non-linear control on the rate of ozone depletion. Model simulations of the volcanic plume chemistry highlight that the proportion of HBr converted into reactive bromine is a key control on the efficiency of ozone depletion. This underlines the importance of chemistry in the very near-source plume on the fate and atmospheric impacts of volcanic emissions to the troposphere.

Adsorption of 2,4-Dichlorophenoxyacetic Acid onto Volcanic Ash Soils:

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Ei Ei Mon

2009-01-01

Full Text Available The quantification of the linear adsorption coefficient (Kd for soils plays a vital role to predict fate and transport of pesticides in the soil-water environment. In this study, we measured Kd values for 2,4-Dichlorophenoxyacetic acid (2,4-D adsorption onto Japanese volcanic ash soils with different amount of soil organic matter (SOM in batch experiments under different pH conditions. All measurements followed well both linear and Freundlich adsorption isotherms. Strong correlations were found between measured Kd values and pH as well as SOM. The 2,4-D adsorption increased with decreasing pH and with increasing SOM. Based on the data, a predictive Kd equation for volcanic ash soils, log (Kd = 2.04 - 0.37 pH + 0.91 log (SOM, was obtained by the multiple regression analysis. The predictive Kd equation was tested against measured 2,4-D sorption data for other volcanic ash soils and normal mineral soils from literature. The proposed Kd equation well predicted Kd values for other volcanic ash soils and slightly over- or under-predicted Kd values for normal mineral soils. The proposed Kd equation performed well against volcanic ash soils from different sites and countries, and is therefore recommended for predicting Kd values at different pH and SOM conditions for volcanic ash soils when calculating and predicting 2,4-D mobility and fate in soil and groundwater.

Observation of SO2 degassing at Stromboli volcano using a hyperspectral thermal infrared imager

Science.gov (United States)

Smekens, Jean-François; Gouhier, Mathieu

2018-05-01

Thermal infrared (TIR) imaging is a common tool for the monitoring of volcanic activity. Broadband cameras with increasing sampling frequency give great insight into the physical processes taking place during effusive and explosive event, while Fourier transform infrared (FTIR) methods provide high resolution spectral information used to assess the composition of volcanic gases but are often limited to a single point of interest. Continuing developments in detector technology have given rise to a new class of hyperspectral imagers combining the advantages of both approaches. In this work, we present the results of our observations of volcanic activity at Stromboli volcano with a ground-based imager, the Telops Hyper-Cam LW, when used to detect emissions of sulfur dioxide (SO2) produced at the vent, with data acquired at Stromboli volcano (Italy) in early October of 2015. We have developed an innovative technique based on a curve-fitting algorithm to quickly extract spectral information from high-resolution datasets, allowing fast and reliable identification of SO2. We show in particular that weak SO2 emissions, such as inter-eruptive gas puffing, can be easily detected using this technology, even with poor weather conditions during acquisition (e.g., high relative humidity, presence of fog and/or ash). Then, artificially reducing the spectral resolution of the instrument, we recreated a variety of commonly used multispectral configurations to examine the efficiency of four qualitative SO2 indicators based on simple Brightness Temperature Difference (BTD). Our results show that quickly changing conditions at the vent - including but not limited to the presence of summit fog - render the establishment of meaningful thresholds for BTD indicators difficult. Building on those results, we propose recommendations on the use of multispectral imaging for SO2 monitoring and routine measurements from ground-based instruments.

Quantification of the CO2 emitted from volcanic lakes in Pico Island (Azores)

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Andrade, César; Cruz, José; Viveiros, Fátima; Branco, Rafael

2017-04-01

This study shows the results of the diffuse CO2 degassing surveys performed in lakes from Pico volcanic Island (Azores archipelago, Portugal). Detailed flux measurements using the accumulation chamber method were made at six lakes (Capitão, Caiado, Paul, Rosada, Peixinho and Negra) during two field campaigns, respectively, in winter (February 2016) and late summer (September 2016). Pico is the second largest island of the Azores archipelago with an area of 444.8 km2; the oldest volcanic unit is dated from about 300,000 years ago. The edification of Pico was mainly due to Hawaiian and Strombolian type volcanic activity, resulting in pahoehoe and aa lava flows of basaltic nature, as well as scoria and spatter cones. Three main volcanic complexes are identified in the island, namely (1) the so-called Montanha Volcanic Complex, corresponding to a central volcano located in the western side of the island that reaches a maximum altitude of 2351 m, (2) the São Roque-Piedade Volcanic Complex, and (3) the Topo-Lajes Volcanic Complex, this last one corresponding to the remnants of a shield volcano located in the south coast. The studied lakes are spread along the São Roque-Piedade Volcanic Complex at altitudes between 785 m and 898 m. Three are associated with depressions of undifferentiated origin (Caiado, Peixinho, Negra), two with depressions of tectonic origin (Capitão, Paul), while Rosada lake is located inside a scoria cone crater. The lakes surface areas vary between 1.25x10-2 and 5.38x10-2 km2, and the water column maximum depth is 7.9 m (3.5-7.9 m). The water storage ranges between 3.6x104 to 9.1x104 m3, and the estimated residence time does not exceed 1.8x10-1 years. A total of 1579 CO2 flux measurements were made during both surveys (868 in summer and 711 in the winter campaign), namely 518 in Caiado lake (293; 225), 358 in Paul (195; 163), 279 in Capitão (150, 129), 200 in Rosada (106, 94), 171 in Peixinho (71, 100) and 53 measurements in Negra lake. Negra

Improving the accuracy of S02 column densities and emission rates obtained from upward-looking UV-spectroscopic measurements of volcanic plumes by taking realistic radiative transfer into account

Science.gov (United States)

Kern, Christoph; Deutschmann, Tim; Werner, Cynthia; Sutton, A. Jeff; Elias, Tamar; Kelly, Peter J.

2012-01-01

Sulfur dioxide (SO2) 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 SO2 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 SO2 plumes.

Next-Generation Aura/OMI NO2 and SO2 Products

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Krotkov, Nickolay; Yang, Kai; Bucsela, Eric; Lamsal, Lok; Celarier, Edward; Swartz, William; Carn, Simon; Bhartia, Pawan; Gleason, James; Pickering, Ken;

Validation Studies of the Accuracy of Various SO2 Gas Retrievals in the Thermal InfraRed (8-14 μm)

Science.gov (United States)

Gabrieli, A.; Wright, R.; Lucey, P. G.; Porter, J. N.; Honniball, C.; Garbeil, H.; Wood, M.

2016-12-01

Quantifying hazardous SO2 in the atmosphere and in volcanic plumes is important for public health and volcanic eruption prediction. Remote sensing measurements of spectral radiance of plumes contain information on the abundance of SO2. However, in order to convert such measurements into SO2 path-concentrations, reliable inversion algorithms are needed. Various techniques can be employed to derive SO2 path-concentrations. The first approach employs a Partial Least Square Regression model trained using MODTRAN5 simulations for a variety of plume and atmospheric conditions. Radiances at many spectral wavelengths (8-14 μm) were used in the algorithm. The second algorithm uses measurements inside and outside the SO2 plume. Measurements in the plume-free region (background sky) make it possible to remove background atmospheric conditions and any instrumental effects. After atmospheric and instrumental effects are removed, MODTRAN5 is used to fit the SO2 spectral feature and obtain SO2 path-concentrations. The two inversion algorithms described above can be compared with the inversion algorithm for SO2 retrievals developed by Prata and Bernardo (2014). Their approach employs three wavelengths to characterize the plume temperature, the atmospheric background, and the SO2 path-concentration. The accuracy of these various techniques requires further investigation in terms of the effects of different atmospheric background conditions. Validating these inversion algorithms is challenging because ground truth measurements are very difficult. However, if the three separate inversion algorithms provide similar SO2 path-concentrations for actual measurements with various background conditions, then this increases confidence in the results. Measurements of sky radiance when looking through SO2 filled gas cells were collected with a Thermal Hyperspectral Imager (THI) under various atmospheric background conditions. These data were processed using the three inversion approaches

Volcanic sulfur dioxide index and volcanic explosivity index inferred from eruptive volume of volcanoes in Jeju Island, Korea: application to volcanic hazard mitigation

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Ko, Bokyun; Yun, Sung-Hyo

2016-04-01

Jeju Island located in the southwestern part of Korea Peninsula is a volcanic island composed of lavaflows, pyroclasts, and around 450 monogenetic volcanoes. The volcanic activity of the island commenced with phreatomagmatic eruptions under subaqueous condition ca. 1.8-2.0 Ma and lasted until ca. 1,000 year BP. For evaluating volcanic activity of the most recently erupted volcanoes with reported age, volcanic explosivity index (VEI) and volcanic sulfur dioxide index (VSI) of three volcanoes (Ilchulbong tuff cone, Songaksan tuff ring, and Biyangdo scoria cone) are inferred from their eruptive volumes. The quantity of eruptive materials such as tuff, lavaflow, scoria, and so on, is calculated using a model developed in Auckland Volcanic Field which has similar volcanic setting to the island. The eruptive volumes of them are 11,911,534 m3, 24,987,557 m3, and 9,652,025 m3, which correspond to VEI of 3, 3, and 2, respectively. According to the correlation between VEI and VSI, the average quantity of SO2 emission during an eruption with VEI of 3 is 2-8 × 103 kiloton considering that the island was formed under intraplate tectonic setting. Jeju Island was regarded as an extinct volcano, however, several studies have recently reported some volcanic eruption ages within 10,000 year BP owing to the development in age dating technique. Thus, the island is a dormant volcano potentially implying high probability to erupt again in the future. The volcanoes might have explosive eruptions (vulcanian to plinian) with the possibility that SO2 emitted by the eruption reaches stratosphere causing climate change due to backscattering incoming solar radiation, increase in cloud reflectivity, etc. Consequently, recommencement of volcanic eruption in the island is able to result in serious volcanic hazard and this study provides fundamental and important data for volcanic hazard mitigation of East Asia as well as the island. ACKNOWLEDGMENTS: This research was supported by a grant [MPSS

A global catalogue of large SO2 sources and emissions derived from the Ozone Monitoring Instrument

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V. E. Fioletov

2016-09-01

Full Text Available Sulfur dioxide (SO2 measurements from the Ozone Monitoring Instrument (OMI satellite sensor processed with the new principal component analysis (PCA algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr−1 to more than 4000 kt yr−1 of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources; power plants (297; smelters (53; and sources related to the oil and gas industry (65. The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005–2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30 % of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80 % over the 2005–2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr−1 and not detected by OMI.

A Global Catalogue of Large SO2 Sources and Emissions Derived from the Ozone Monitoring Instrument

Science.gov (United States)

Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.

2016-01-01

Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr(exp -1) to more than 4000 kt yr(exp -1) of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005- 2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30% of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80% over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr(exp -1) and not detected by OMI.

Sulfur dioxide (SO2 from MIPAS in the upper troposphere and lower stratosphere 2002–2012

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M. Höpfner

2015-06-01

Full Text Available Vertically resolved distributions of sulfur dioxide (SO2 with global coverage in the height region from the upper troposphere to ~20 km altitude have been derived from observations by the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS on Envisat for the period July 2002 to April 2012. Retrieved volume mixing ratio profiles representing single measurements are characterized by typical errors in the range of 70–100 pptv and by a vertical resolution ranging from 3 to 5 km. Comparison with observations by the Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS revealed a slightly varying bias with altitude of −20 to 50 pptv for the MIPAS data set in case of volcanically enhanced concentrations. For background concentrations the comparison showed a systematic difference between the two major MIPAS observation periods. After debiasing, the difference could be reduced to biases within −10 to 20 pptv in the altitude range of 10–20 km with respect to ACE-FTS. Further comparisons of the debiased MIPAS data set with in situ measurements from various aircraft campaigns showed no obvious inconsistencies within a range of around ±50 pptv. The SO2 emissions of more than 30 volcanic eruptions could be identified in the upper troposphere and lower stratosphere (UTLS. Emitted SO2 masses and lifetimes within different altitude ranges in the UTLS have been derived for a large part of these eruptions. Masses are in most cases within estimations derived from other instruments. From three of the major eruptions within the MIPAS measurement period – Kasatochi in August 2008, Sarychev in June 2009 and Nabro in June 2011 – derived lifetimes of SO2 for the altitude ranges 10–14, 14–18 and 18–22 km are 13.3 ± 2.1, 23.6 ± 1.2 and 32.3 ± 5.5 days respectively. By omitting periods with obvious volcanic influence we have derived background mixing ratio distributions of SO2. At 10 km altitude these indicate an annual

Improving retrieval of volcanic sulphur dioxide from backscattered UV satellite observations

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Yang, Kai; Krotkov, N.A.; Krueger, A.J.; Carn, S.A.; Bhartia, P.K.; Levelt, P.F.

2009-01-01

Existing algorithms that use satellite measurements of solar backscattered ultraviolet (BUV) radiances to retrieve sulfur dioxide (SO2) vertical columns underestimate the large SO2 amounts encountered in fresh volcanic eruption clouds. To eliminate this underestimation we have developed a new

Periodicity in the BrO/SO2 molar ratios in the volcanic gas plume of Cotopaxi and its correlation with the Earth tides during the eruption in 2015

Science.gov (United States)

Dinger, Florian; Bobrowski, Nicole; Warnach, Simon; Bredemeyer, Stefan; Hidalgo, Silvana; Arellano, Santiago; Galle, Bo; Platt, Ulrich; Wagner, Thomas

2018-03-01

We evaluated NOVAC (Network for Observation of Volcanic and Atmospheric Change) gas emission data from the 2015 eruption of the Cotopaxi volcano (Ecuador) for BrO/SO2 molar ratios. The BrO/SO2 molar ratios were very small prior to the phreatomagmatic explosions in August 2015, significantly higher after the explosions, and continuously increasing until the end of the unrest period in December 2015. These observations together with similar findings in previous studies at other volcanoes (Mt. Etna, Nevado del Ruiz, Tungurahua) suggest a possible link between a drop in BrO/SO2 and a future explosion. In addition, the observed relatively high BrO/SO2 molar ratios after December 2015 imply that bromine degassed predominately after sulfur from the magmatic melt. Furthermore, statistical analysis of the data revealed a conspicuous periodic pattern with a periodicity of about 2 weeks in a 3-month time series. While the time series is too short to rule out a chance recurrence of transient geological or meteorological events as a possible origin for the periodic signal, we nevertheless took this observation as a motivation to examine the influence of natural forcings with periodicities of around 2 weeks on volcanic gas emissions. One strong aspirant with such a periodicity are the Earth tides, which are thus central in this study. We present the BrO/SO2 data, analyse the reliability of the periodic signal, discuss a possible meteorological or eruption-induced origin of this signal, and compare the signal with the theoretical ground surface displacement pattern caused by the Earth tides. Our central result is the observation of a significant correlation between the BrO/SO2 molar ratios with the north-south and vertical components of the calculated tide-induced surface displacement with correlation coefficients of 47 and 36 %, respectively. From all other investigated parameters, only the correlation between the BrO/SO2 molar ratios and the relative humidity in the local

OMI measurements of SO2 pollution over Eastern China in 2005-2008

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Krotkov, N.; Pickering, K.; Witte, J.; Carn, S.; Yang, K.; Carmichael, G.; Streets, D.; Zhang, Q.; Wei, C.

2009-05-01

The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. OMI seasonal to multi-year average images clearly show the world-highest consistent SO2 pollution in northeast China. China is the world's largest SO2 emitter, mostly due to the burning of high-sulfur coal in its many coal-fired power plants, which lack the technology used in many other countries to remove sulfur from smoke stack emissions. China's government has instituted nationwide measures to control SO2 emissions through the adoption of flue-gas desulfurization technology on new power plants; and even greater measures were adopted in the Beijing area in anticipation of the Olympic Games. To study the environmental effects of the emission controls we compared OMI SO2 time series over eastern China for 2005 through 2008. The time series have been done as 7-day running means of the cloud-free daily observations. By mid-March we started to see substantial periods of lower SO2 values in 2008 compared to 2007, and by mid June the 2008 values were consistently lower than 2007 and prior years. The decline is widespread with highest SO2 typically located to the south and southwest of Beijing in regions with large clusters of power plants and also around Shanghai. The decline also lasted beyond the Olympic season. We do not yet know to what extent the economic downturn in China (and reduced industrial production) contributed to lower SO2 levels in the fall of 2008. We have also compared the observed and modeled fields using University of Iowa STEM model for the period June - September 2008. The model provided SO2 vertical distributions as well as aerosol vertical profiles that were used to correct OMI operational SO2 retrievals and improve the comparisons. The OMI SO2 changes in 2008 have also been compared with the estimated changes in SO2 emissions

Effect of volcanic aerosol on stratospheric NO2 and N2O5 from 2002–2014 as measured by Odin-OSIRIS and Envisat-MIPAS

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C. Adams

2017-07-01

Full Text Available Following the large volcanic eruptions of Pinatubo in 1991 and El Chichón in 1982, decreases in stratospheric NO2 associated with enhanced aerosol were observed. The Optical Spectrograph and Infrared Imaging Spectrometer (OSIRIS measured the widespread enhancements of stratospheric aerosol following seven volcanic eruptions between 2002 and 2014, although the magnitudes of these eruptions were all much smaller than the Pinatubo and El Chichón eruptions. In order to isolate and quantify the relationship between volcanic aerosol and NO2, NO2 anomalies were calculated using measurements from OSIRIS and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS. In the tropics, variability due to the quasi-biennial oscillation was subtracted from the time series. OSIRIS profile measurements indicate that the strongest anticorrelations between NO2 and volcanic aerosol extinction were for the 5 km layer starting  ∼  3 km above the climatological mean tropopause at the given latitude. OSIRIS stratospheric NO2 partial columns in this layer were found to be smaller than background NO2 levels during these aerosol enhancements by up to  ∼  60 % with typical Pearson correlation coefficients of R ∼ −0. 7. MIPAS also observed decreases in NO2 partial columns during periods affected by volcanic aerosol, with percent differences of up to  ∼  25 % relative to background levels. An even stronger anticorrelation was observed between OSIRIS aerosol optical depth and MIPAS N2O5 partial columns, with R ∼ −0. 9, although no link with MIPAS HNO3 was observed. The variation in OSIRIS NO2 with increasing aerosol was found to be consistent with simulations from a photochemical box model within the estimated model uncertainty.

Real-time, high frequency (1 Hz), in situ measurement of HCl and HF gases in volcanic plumes with a novel cavity-enhanced, laser-based instrument

Science.gov (United States)

Kelly, P. J.; Sutton, A. J.; Elias, T.; Kern, C.; Clor, L. E.; Baer, D. S.

2017-12-01

Primary magmatic halogen-containing gases (HCl, HF, HBr, HI in characteristic order of abundance) are of great interest for volcano monitoring and research because, in general, they are more soluble in magma than other commonly-monitored volcanic volatiles (e.g. CO2, SO2, H2S) and thereby can offer unique insights into shallow magmatic processes. Nevertheless, difficulties in obtaining observations of primary volcanic halogens in gas plumes with traditional methods (e.g. direct sampling, Open-Path Fourier Transform Infrared spectroscopy, filter packs) have limited the number of observations reported worldwide, especially from explosive arc volcanoes. With this in mind, the USGS and Los Gatos Research, Inc. collaborated to adapt a commercially-available industrial in situ HCl-HF analyzer for use in airborne and ground-based measurements of volcanic gases. The new, portable instrument is based around two near-IR tunable diode lasers and uses a vibration-tolerant, enhanced-cavity approach that is well-suited for rugged field applications and yields fast (1 Hz) measurements with a wide dynamic range (0 -2 ppm) and sub-ppb precision (1σ: HCl: <0.4 ppb; HF: <0.1 ppb). In spring 2017 we conducted field tests at Kīlauea Volcano, Hawaii, to benchmark the performance of the new instrument and to compare it with an accepted method for halogen measurements (OP-FTIR). The HCl-HF instrument was run in parallel with a USGS Multi-GAS to obtain in situ H2O-CO2-SO2-H2S-HCl-HF plume compositions. The results were encouraging and quasi-direct comparisons of the in situ and remote sensing instruments showed good agreement (e.g. in situ SO2/HCl = 72 vs. OP-FTIR SO2/HCl = 88). Ground-based and helicopter-based measurements made 0 - 12 km downwind from the vent (plume age 0 - 29 minutes) show that plume SO2/HCl ratios increase rapidly from 60 to 300 around the plume edges, possibly due to uptake of HCl onto aerosols.

Global volcanic emissions: budgets, plume chemistry and impacts

Science.gov (United States)

Mather, T. A.

2012-12-01

Over the past few decades our understanding of global volcanic degassing budgets, plume chemistry and the impacts of volcanic emissions on our atmosphere and environment has been revolutionized. Global volcanic emissions budgets are needed if we are to make effective use of regional and global atmospheric models in order to understand the consequences of volcanic degassing on global environmental evolution. Traditionally volcanic SO2 budgets have been the best constrained but recent efforts have seen improvements in the quantification of the budgets of other environmentally important chemical species such as CO2, the halogens (including Br and I) and trace metals (including measurements relevant to trace metal atmospheric lifetimes and bioavailability). Recent measurements of reactive trace gas species in volcanic plumes have offered intriguing hints at the chemistry occurring in the hot environment at volcanic vents and during electrical discharges in ash-rich volcanic plumes. These reactive trace species have important consequences for gas plume chemistry and impacts, for example, in terms of the global fixed nitrogen budget, volcanically induced ozone destruction and particle fluxes to the atmosphere. Volcanically initiated atmospheric chemistry was likely to have been particularly important before biological (and latterly anthropogenic) processes started to dominate many geochemical cycles, with important consequences in terms of the evolution of the nitrogen cycle and the role of particles in modulating the Earth's climate. There are still many challenges and open questions to be addressed in this fascinating area of science.

Periodicity in the BrO∕SO2 molar ratios in the volcanic gas plume of Cotopaxi and its correlation with the Earth tides during the eruption in 2015

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F. Dinger

2018-03-01

Full Text Available We evaluated NOVAC (Network for Observation of Volcanic and Atmospheric Change gas emission data from the 2015 eruption of the Cotopaxi volcano (Ecuador for BrO∕SO2 molar ratios. The BrO∕SO2 molar ratios were very small prior to the phreatomagmatic explosions in August 2015, significantly higher after the explosions, and continuously increasing until the end of the unrest period in December 2015. These observations together with similar findings in previous studies at other volcanoes (Mt. Etna, Nevado del Ruiz, Tungurahua suggest a possible link between a drop in BrO∕SO2 and a future explosion. In addition, the observed relatively high BrO∕SO2 molar ratios after December 2015 imply that bromine degassed predominately after sulfur from the magmatic melt. Furthermore, statistical analysis of the data revealed a conspicuous periodic pattern with a periodicity of about 2 weeks in a 3-month time series. While the time series is too short to rule out a chance recurrence of transient geological or meteorological events as a possible origin for the periodic signal, we nevertheless took this observation as a motivation to examine the influence of natural forcings with periodicities of around 2 weeks on volcanic gas emissions. One strong aspirant with such a periodicity are the Earth tides, which are thus central in this study. We present the BrO∕SO2 data, analyse the reliability of the periodic signal, discuss a possible meteorological or eruption-induced origin of this signal, and compare the signal with the theoretical ground surface displacement pattern caused by the Earth tides. Our central result is the observation of a significant correlation between the BrO∕SO2 molar ratios with the north–south and vertical components of the calculated tide-induced surface displacement with correlation coefficients of 47 and 36 %, respectively. From all other investigated parameters, only the correlation between the BrO∕SO2 molar

SO2 over Central China: Measurements, Numerical Simulations and the Tropospheric Sulfur Budget

Science.gov (United States)

He, Hao; Li, Can; Loughner, Christopher P.; Li, Zhangqing; Krotkov, Nickolay A.; Yang, Kai; Wang, Lei; Zheng, Youfei; Bao, Xiangdong; Zhao, Guoqiang;

Decade of stratospheric sulfate measurements compared with observations of volcanic eruptions

International Nuclear Information System (INIS)

Sedlacek, W.A.; Mroz, E.J.; Lazrus, A.L.; Gandrud, B.W.

1983-01-01

Sulfate aerosol concentrations in the stratosphere have been measured for 11 years (1971--1981) using portions of filters collected by the Department of Energy's High Altitude Sampling Program. Data collected seasonally at altitudes between 13 km and 20 km spanning latitudes from 75 0 N to 51 0 S are reported. These data are compared with the reported altitudes of volcanic eruption plumes during the same decade. From this comparison it is concluded that (1) several unreported volcanic eruptions or eruptions to altitudes higher than reported did occur during the decade, (2) the e-fold removal time for sulfate aerosol from the stratosphere following the eruption of Volcan Fuego in 1974 was 11.2 +- 1.2 months, (3) the volcanic contribution to the average stratospheric sulfate concentration over the decade was greater than 50%, and (4) there may be evidence for an anthropogenic contribution to stratospheric sulfate that increases at the rate of 6 to 8% per year

UV Fourier transform measurements of tropospheric O3, NO2, SO2, benzene, and toluene

International Nuclear Information System (INIS)

Vandaele, A.C.; Tsouli, A.; Carleer, M.; Colin, R.

2002-01-01

Using the differential optical absorption spectroscopy (DOAS) technique and a Fourier transform spectrometer, NO 2 , SO 2 , O 3 , benzene, and toluene were measured during three measurement campaigns held in Brussels in 1995, 1996, and 1997. The O 3 concentrations could be explained as the results of the local photochemistry and the dynamical properties of the mixing layer. NO 2 concentrations were anti-correlated to the O 3 concentrations, is expected. SO 2 also showed a pronounced dependence on car traffic. Average benzene and toluene concentrations were, respectively 1.7 ppb and between 4.4 and 6.6 pbb, but high values of toluene up to 98.8 ppb were observed. SO 2 concentrations and to a lesser extent, those of NO 2 and O 3 , were dependent on the wind direction. Ozone in Brussels has been found to be influenced by the meteorological conditions prevailing in central Europe. Comparisons with other measurements have shown that O 3 and SO 2 data are in general in good agreement, but our NO 2 concentrations seem to be generally higher. (author)

Satellite-based detection of volcanic sulphur dioxide from recent eruptions in Central and South America

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D. Loyola

2008-01-01

Full Text Available Volcanic eruptions can emit large amounts of rock fragments and fine particles (ash into the atmosphere, as well as several gases, including sulphur dioxide (SO₂. These ejecta and emissions are a major natural hazard, not only to the local population, but also to the infrastructure in the vicinity of volcanoes and to aviation. Here, we describe a methodology to retrieve quantitative information about volcanic SO₂ plumes from satellite-borne measurements in the UV/Visible spectral range. The combination of a satellite-based SO₂ detection scheme and a state-of-the-art 3D trajectory model enables us to confirm the volcanic origin of trace gas signals and to estimate the plume height and the effective emission height. This is demonstrated by case-studies for four selected volcanic eruptions in South and Central America, using the GOME, SCIAMACHY and GOME-2 instruments.

The Eyjafjallajökull eruption in April 2010 – detection of volcanic plume using in-situ measurements, ozone sondes and lidar-ceilometer profiles

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H. Flentje

2010-10-01

Full Text Available Volcanic emissions from the Eyjafjallajökull volcano eruption on the Southern fringe of Iceland in April 2010 were detected at the Global Atmosphere Watch (GAW station Zugspitze/Hohenpeissenberg (Germany by means of in-situ measurements, ozone sondes and ceilometers. Information from the German Meteorological Service (DWD ceilometer network (Flentje et al., 2010 aided identifying the air mass origin. We discuss ground level in-situ measurements of sulphur dioxide (SO₂, sulphuric acid (H₂SO₄ and particulate matter as well as ozone sonde profiles and column measurements of SO₂ by a Brewer spectrometer. At Hohenpeissenberg, a number of reactive gases, e.g. carbon monoxide and nitrogen oxides, and particle properties, e.g. size distribution and ionic composition, were additionally measured during this period. Our results describe the arrival of the volcanic plume at Zugspitze and Hohenpeissenberg during 16 and 17 April 2010 and its residence in the planetary boundary layer (PBL for several days thereafter. The ash plume was first seen in the ceilometer backscatter profiles at Hohenpeissenberg in about 6–7 km altitude. After entrainment into the PBL at noon of 17 April, largely enhanced values of sulphur dioxide, sulphuric acid and super-micron-particle number concentration were recorded at Zugspitze/Hohenpeissenberg till 21 April.

Soil CO2 flux baseline in an urban monogenetic volcanic field: the Auckland Volcanic Field, New Zealand

Science.gov (United States)

Mazot, Agnès; Smid, Elaine R.; Schwendenmann, Luitgard; Delgado-Granados, Hugo; Lindsay, Jan

2013-11-01

The Auckland Volcanic Field (AVF) is a dormant monogenetic basaltic field located in Auckland, New Zealand. Though soil gas CO2 fluxes are routinely used to monitor volcanic regions, there have been no published studies of soil CO2 flux or soil gas CO2 concentrations in the AVF to date or many other monogenetic fields worldwide. We measured soil gas CO2 fluxes and soil gas CO2 concentrations in 2010 and 2012 in varying settings, seasons, and times of day to establish a baseline soil CO2 flux and to determine the major sources of and controlling influences on Auckland's soil CO2 flux. Soil CO2 flux measurements varied from 0 to 203 g m-2 day-1, with an average of 27.1 g m-2 day-1. Higher fluxes were attributed to varying land use properties (e.g., landfill). Using a graphical statistical approach, two populations of CO2 fluxes were identified. Isotope analyses of δ13CO2 confirmed that the source of CO2 in the AVF is biogenic with no volcanic component. These data may be used to assist with eruption forecasting in the event of precursory activity in the AVF, and highlight the importance of knowing land use history when assessing soil gas CO2 fluxes in urban environments.

Using Himawari-8, estimation of SO2 cloud altitude at Aso volcano eruption, on October 8, 2016

Science.gov (United States)

Ishii, Kensuke; Hayashi, Yuta; Shimbori, Toshiki

2018-02-01

It is vital to detect volcanic plumes as soon as possible for volcanic hazard mitigation such as aviation safety and the life of residents. Himawari-8, the Japan Meteorological Agency's (JMA's) geostationary meteorological satellite, has high spatial resolution and sixteen observation bands including the 8.6 μm band to detect sulfur dioxide (SO2). Therefore, Ash RGB composite images (RED: brightness temperature (BT) difference between 12.4 and 10.4 μm, GREEN: BT difference between 10.4 and 8.6 μm, BLUE: 10.4 μm) discriminate SO2 clouds and volcanic ash clouds from meteorological clouds. Since the Himawari-8 has also high temporal resolution, the real-time monitoring of ash and SO2 clouds is of great use. A phreatomagmatic eruption of Aso volcano in Kyushu, Japan, occurred at 01:46 JST on October 8, 2016. For this eruption, the Ash RGB could detect SO2 cloud from Aso volcano immediately after the eruption and track it even 12 h after. In this case, the Ash RGB images every 2.5 min could clearly detect the SO2 cloud that conventional images such as infrared and split window could not detect sufficiently. Furthermore, we could estimate the height of the SO2 cloud by comparing the Ash RGB images and simulations of the JMA Global Atmospheric Transport Model with a variety of height parameters. As a result of comparison, the top and bottom height of the SO2 cloud emitted from the eruption was estimated as 7 and 13-14 km, respectively. Assuming the plume height was 13-14 km and eruption duration was 160-220 s (as estimated by seismic observation), the total emission mass of volcanic ash from the eruption was estimated as 6.1-11.8 × 108 kg, which is relatively consistent with 6.0-6.5 × 108 kg from field survey. [Figure not available: see fulltext.

Improving global detection of volcanic eruptions using the Ozone Monitoring Instrument (OMI

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V. J. B. Flower

2016-11-01

Full Text Available Volcanic eruptions pose an ever-present threat to human populations around the globe, but many active volcanoes remain poorly monitored. In regions where ground-based monitoring is present the effects of volcanic eruptions can be moderated through observational alerts to both local populations and service providers, such as air traffic control. However, in regions where volcano monitoring is limited satellite-based remote sensing provides a global data source that can be utilised to provide near-real-time identification of volcanic activity. This paper details a volcanic plume detection method capable of identifying smaller eruptions than is currently feasible, which could potentially be incorporated into automated volcanic alert systems. This method utilises daily, global observations of sulfur dioxide (SO2 by the Ozone Monitoring Instrument (OMI on NASA's Aura satellite. Following identification and classification of known volcanic eruptions in 2005–2009, the OMI SO2 data, analysed using a logistic regression analysis, permitted the correct classification of volcanic events with an overall accuracy of over 80 %. Accurate volcanic plume identification was possible when lower-tropospheric SO2 loading exceeded ∼ 400 t. The accuracy and minimal user input requirements of the developed procedure provide a basis for incorporation into automated SO2 alert systems.

Global volcanic aerosol properties derived from emissions, 1990-2014, using CESM1(WACCM): VOLCANIC AEROSOLS DERIVED FROM EMISSIONS

Energy Technology Data Exchange (ETDEWEB)

Mills, Michael J. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Schmidt, Anja [School of Earth and Environment, University of Leeds, Leeds UK; Easter, Richard [Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland Washington USA; Solomon, Susan [Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, Cambridge Massachusetts USA; Kinnison, Douglas E. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Ghan, Steven J. [Atmospheric Sciences and Global Change Division, Pacific Northwest National Laboratory, Richland Washington USA; Neely, Ryan R. [School of Earth and Environment, University of Leeds, Leeds UK; National Centre for Atmospheric Science, University of Leeds, Leeds UK; Marsh, Daniel R. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Conley, Andrew [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Bardeen, Charles G. [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA; Gettelman, Andrew [Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder Colorado USA

2016-03-06

Accurate representation of global stratospheric aerosol properties from volcanic and non-volcanic sulfur emissions is key to understanding the cooling effects and ozone-loss enhancements of recent volcanic activity. Attribution of climate and ozone variability to volcanic activity is of particular interest in relation to the post-2000 slowing in the apparent rate of global average temperature increases, and variable recovery of the Antarctic ozone hole. We have developed a climatology of global aerosol properties from 1990 to 2014 calculated based on volcanic and non-volcanic emissions of sulfur sources. We have complied a database of volcanic SO2 emissions and plume altitudes for eruptions between 1990 and 2014, and a new prognostic capability for simulating stratospheric sulfate aerosols in version 5 of the Whole Atmosphere Community Climate Model, a component of the Community Earth System Model. Our climatology shows remarkable agreement with ground-based lidar observations of stratospheric aerosol optical depth (SAOD), and with in situ measurements of aerosol surface area density (SAD). These properties are key parameters in calculating the radiative and chemical effects of stratospheric aerosols. Our SAOD climatology represents a significant improvement over satellite-based analyses, which ignore aerosol extinction below 15 km, a region that can contain the vast majority of stratospheric aerosol extinction at mid- and high-latitudes. Our SAD climatology significantly improves on that provided for the Chemistry-Climate Model Initiative, which misses 60% of the SAD measured in situ. Our climatology of aerosol properties is publicly available on the Earth System Grid.

PHOTOCHEMISTRY IN TERRESTRIAL EXOPLANET ATMOSPHERES. II. H{sub 2}S AND SO{sub 2} PHOTOCHEMISTRY IN ANOXIC ATMOSPHERES

Energy Technology Data Exchange (ETDEWEB)

Hu Renyu; Seager, Sara; Bains, William, E-mail: hury@mit.edu [Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139 (United States)

2013-05-20

Sulfur gases are common components in the volcanic and biological emission on Earth, and are expected to be important input gases for atmospheres on terrestrial exoplanets. We study the atmospheric composition and the spectra of terrestrial exoplanets with sulfur compounds (i.e., H{sub 2}S and SO{sub 2}) emitted from their surfaces. We use a comprehensive one-dimensional photochemistry model and radiative transfer model to investigate the sulfur chemistry in atmospheres ranging from reducing to oxidizing. The most important finding is that both H{sub 2}S and SO{sub 2} are chemically short-lived in virtually all types of atmospheres on terrestrial exoplanets, based on models of H{sub 2}, N{sub 2}, and CO{sub 2} atmospheres. This implies that direct detection of surface sulfur emission is unlikely, as their surface emission rates need to be extremely high (>1000 times Earth's volcanic sulfur emission) for these gases to build up to a detectable level. We also find that sulfur compounds emitted from the surface lead to photochemical formation of elemental sulfur and sulfuric acid in the atmosphere, which would condense to form aerosols if saturated. For terrestrial exoplanets in the habitable zone of Sun-like stars or M stars, Earth-like sulfur emission rates result in optically thick haze composed of elemental sulfur in reducing H{sub 2}-dominated atmospheres for a wide range of particle diameters (0.1-1 {mu}m), which is assumed as a free parameter in our simulations. In oxidized atmospheres composed of N{sub 2} and CO{sub 2}, optically thick haze, composed of elemental sulfur aerosols (S{sub 8}) or sulfuric acid aerosols (H{sub 2}SO{sub 4}), will form if the surface sulfur emission is two orders of magnitude more than the volcanic sulfur emission of Earth. Although direct detection of H{sub 2}S and SO{sub 2} by their spectral features is unlikely, their emission might be inferred by observing aerosol-related features in reflected light with future generation

Sulfur dioxide (SO2 as observed by MIPAS/Envisat: temporal development and spatial distribution at 15–45 km altitude

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M. Höpfner

2013-10-01

Full Text Available We present a climatology of monthly and 10° zonal mean profiles of sulfur dioxide (SO2 volume mixing ratios (vmr derived from MIPAS/Envisat measurements in the altitude range 15–45 km from July 2002 until April 2012. The vertical resolution varies from 3.5–4 km in the lower stratosphere up to 6–10 km at the upper end of the profiles, with estimated total errors of 5–20 pptv for single profiles of SO2. Comparisons with the few available observations of SO2 up to high altitudes from ATMOS for a volcanically perturbed situation from ACE-FTS and, at the lowest altitudes, with stratospheric in situ observations reveal general consistency of the datasets. The observations are the first empirical confirmation of features of the stratospheric SO2 distribution, which have only been shown by models up to now: (1 the local maximum of SO2 at around 25–30 km altitude, which is explained by the conversion of carbonyl sulfide (COS as the precursor of the Junge layer; and (2 the downwelling of SO2-rich air to altitudes of 25–30 km at high latitudes during winter and its subsequent depletion on availability of sunlight. This has been proposed as the reason for the sudden appearance of enhanced concentrations of condensation nuclei during Arctic and Antarctic spring. Further, the strong increase of SO2 to values of 80–100 unit{pptv} in the upper stratosphere through photolysis of H2SO4 has been confirmed. Lower stratospheric variability of SO2 could mainly be explained by volcanic activity, and no hints of a strong anthropogenic influence have been found. Regression analysis revealed a QBO (quasi-biennial oscillation signal of the SO2 time series in the tropics at about 30–35 km, an SAO (semi-annual oscillation signal at tropical and subtropical latitudes above 32 km and annual periodics predominantly at high latitudes. Further, the analysis indicates a correlation with the solar cycle in the tropics and southern subtropics above 30 km

Volcanic fluxes of volatiles. Preliminary estimates based on rare gas and major volatile calibration

International Nuclear Information System (INIS)

Marty, B.

1992-01-01

New estimates for volatile fluxes into the atmosphere and hydrosphere through volcanism have been computed using the measured fluxes of 3 He in oceans and SO 2 in the atmosphere, and the ratios between the volatiles in Mid-Ocean Ridge basalts and in high temperature volcanic gases. These estimates have been checked using independent estimates of the volcanic fluxes. This method provides a reliable means of tracing volatile fluxes, although its precision is restricted by the limited amount of data currently available. (author). 19 refs, 1 tab

Field test of available methods to measure remotely SO2 and NOx emissions from ships

Science.gov (United States)

Balzani Lööv, J. M.; Alfoldy, B.; Beecken, J.; Berg, N.; Berkhout, A. J. C.; Duyzer, J.; Gast, L. F. L.; Hjorth, J.; Jalkanen, J.-P.; Lagler, F.; Mellqvist, J.; Prata, F.; van der Hoff, G. R.; Westrate, H.; Swart, D. P. J.; Borowiak, A.

2013-11-01

Methods for the determination of ship fuel sulphur content and NOx emission factors from remote measurements have been compared in the harbour of Rotterdam and compared to direct stack emission measurements on the ferry Stena Hollandica. The methods were selected based on a review of the available literature on ship emission measurements. They were either optical (LIDAR, DOAS, UV camera), combined with model based estimates of fuel consumption, or based on the so called "sniffer" principle, where SO2 or NOx emission factors are determined from simultaneous measurement of the increase of CO2 and SO2 or NOx concentrations in the plume of the ship compared to the background. The measurements were performed from stations at land, from a boat, and from a helicopter. Mobile measurement platforms were found to have important advantages compared to the landbased ones because they allow to optimize the sampling conditions and to sample from ships on the open sea. Although optical methods can provide reliable results, it was found that at the state of the art, the "sniffer" approach is the most convenient technique for determining both SO2 and NOx emission factors remotely. The average random error on the determination of SO2 emission factors comparing two identical instrumental set-ups was 6%. However, it was found that apparently minor differences in the instrumental characteristics, such as response time, could cause significant differences between the emission factors determined. Direct stack measurements showed that about 14% of the fuel sulphur content was not emitted as SO2. This was supported by the remote measurements and is in agreement with the results of other field studies.

Long range transport and air quality impacts of SO2 emissions from Holuhraun (Bárdarbunga, Iceland)

Science.gov (United States)

Schmidt, Anja; Witham, Claire; Leadbetter, Susan; Theys, Nicholas; Hort, Matthew; Thordarson, Thorvaldur; Stevenson, John; Shepherd, Janet; Sinnott, Richard; Kenny, Patrick; Barsotti, Sara

2015-04-01

Gas emissions from the Holuhraun eruption site in Iceland resulted in increases in observed ground level concentrations of sulphur dioxide (SO2) in the UK and Ireland during two occasions in September 2014. We present data from the Irish and UK monitoring networks along with satellite imagery which describes the temporal and spatial evolution of these pollution episodes. During both events increases in concentration were significant compared to ambient levels. The peaks were short lived, 6-12 hours, and below the World Health Organisation's 10-minute air quality standard for SO2 of 500 µg/m3, but these events show that gas from relatively low altitude volcanic emissions in Iceland can pose a hazard to north west Europe. The two pollution events serve as excellent case studies and observations from the events provide us with a unique dataset for the verification of atmospheric dispersion models. We use the atmospheric dispersion model NAME to simulate the long-range transport, removal and chemical conversion of the volcanic SO2 during September 2014. We evaluate a range of model simulations, using varying model input and physical parameters, against ground based measurements and satellite retrievals of SO2. Simulations demonstrate that the long-range ground concentrations are strongly dependent on the emission flux and the height of emission at source. This relationship is well known from similar studies of other pollution events. However this work also demonstrates a dependence on the model's vertical turbulence parameterisation and the height of the boundary layer determined from the input Numerical Weather Prediction meteorological data. For the pollution events in September 2014, we find that using a mass flux of 40 kilotons per day of SO2 gives best agreement with vertical column retrievals of SO2 from the Ozone Monitoring Instrument, which is in good agreement with initial estimates made by the Icelandic Meteorological Office. "This work is distributed under

K-Ar ages of the Neogene volcanic rocks from the Oshamambe district, southwestern Hokkaido

International Nuclear Information System (INIS)

Kubo, Kazuya; Shibata, Ken; Ishida, Masao

1988-01-01

Oshamanbe district is on the northern extension of the so-called green tuff district in northeastern Japan, and the sedimentary rocks in a sea area and volcanic rocks from Miocene to Pleistocene widely distribute. The authors carried out the geological survey of this district, and published the results as the geological features in Oshamanbe district. The volcanic rocks distributing in this district range from andesite to dacite and rhyolite. Their lithofacies are mostly volcanic breccia and tuff breccia, accompanied by lava and dikes. This time, the measurement of the age of these volcanic rocks was carried out, and the stratigraphical table made by the authors was investigated. It is considered that those age values offer important information for determining the age of the Setana formation. The outline of the geological features, the samples for the measurement, the method of measurement of Ar isotopic ratio and K, and the results of measurement are reported. As the results, 4.38 - 4.47 Ma were obtained for Garogawa volcanic rocks, and 2.59 Ma for Shamanbesan volcanic rocks. The period of sedimentation of the Setana formation was from the latter period of Pliocene to pleistocene. (Kako, I.)

CO2, SO2, and H2S Degassing Related to the 2009 Redoubt Eruption, Alaska

Science.gov (United States)

Werner, C. A.; Kelly, P. J.; Evans, W.; Doukas, M. P.; McGimsey, R. G.; Neal, C. A.

2012-12-01

The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions with 35 airborne measurements of CO2, SO2, and H2S that span from October 2008 to August 2010. Increases in CO2 degassing were detected up to 5 months prior to the eruption and varied between 3630 and 9020 tonnes per day (t/d) in the 6 weeks prior to the eruption. Increased pre-eruptive CO2 degassing was accompanied by comparatively low S emission, resulting in molar C/S ratios that ranged between 30-60. However, the C/S ratio dropped to 2.4 coincident with the first phreatic explosion on March 15, 2009, and remained steady during the explosive (March 22 - April 4, 2009), effusive dome-building (April 5 - July 1, 2009), and waning phases (August 2009 onward) of the eruption. Observations of ice-melt rates, melt water discharge, and water chemistry in the months leading up to the eruption suggested that surface waters represented drainage from surficial, perched reservoirs of condensed magmatic steam and glacial meltwater. While the surface waters were capable of scrubbing many thousands of t/d of SO2, sampling of these fluids revealed that only a few hundred tonnes of SO2 was reacting to a dissolved component each day. This is also much less than the ~ 2100 t/d SO2 expected from degassing of magma in the upper crust (3-6.5 km), where petrologic analysis shows the final magma equilibration occurred. Thus, the high pre-eruptive C/S ratios observed could reflect bulk degassing of upper-crustal magma followed by nearly complete loss of SO2 in a magmatic-hydrothermal system. Alternatively, high C/S ratios could be attributed to degassing of low silica andesitic magma that intruded into the mid-crust in the 5 months prior to eruption; modeling suggests that mixing of this magma with pre-existing high silica andesite magma or mush would have caused a reduction of the C/S ratio to a value consistent with that measured during the eruption. Monitoring emissions regularly

Volcanic Ash Impacts on Air Traffic from the 2009 Mt. Redoubt Eruption

Science.gov (United States)

Murray, J. J.; Matus, A. V.; Hudnall, L. A.; Krueger, A. J.; Haynes, J. A.; Pippin, M. R.

2009-12-01

The dispersion of volcanic ash during the March 2009 eruption of Mt. Redoubt created the potential for major problems for aviation. Mt. Redoubt is located 110 km west-southwest of Alaska Airlines hub in Anchorage. It last erupted in 1990 and caused an estimated $101 million cost to the aviation industry (Waythomas, 1998). This study was conducted to assist in improving warning systems, policy and procedures for addressing the impact of volcanic ash on aviation. The study had two primary components. First, the altitude and extent of SO2 dispersion was determined through analysis of synoptic meteorological conditions and satellite imagery. Second, impacts on aviation from the volcanic ash dispersion were investigated. OMI SO2 column measurements were employed to assess the altitude and extent of SO2 dispersion of volcanic ash. To accomplish this, OMI data were assimilated with CALIPSO backscatter profiles, geopotential height plots, and HYSPLIT forward model trajectories. Volcanic Ash Advisories were compared to airport and pilot reports to assess aviation impacts. The eruption produced a complex dispersion of volcanic ash. Volcanic ash altitudes estimated for 23 March 2009 indicate that the majority of the plume remained at approximately 8 km, although reports indicate that the initial plume may have reached as high as18 km (60,000 ft). A low pressure system which passed over the eruption area appears to have entrained most of the ash at approximately 8 km, however the CALIPSO satellite indicates that dispersion also extended to 10 km and 16 km. Atmospheric patterns suggest dispersion at approximately 3 km near Hudson Bay. Analysis of 25 March 2009 indicates that much of the ash plume was dispersed at higher altitudes, where CALIPSO data locates the stratospheric ash plume at approximately 14 km above mean sea level. By the time the eruptions had subsided in April, Alaska Airlines had cancelled 295 flights and disrupted the flights of over 20,000 passengers. This

The Origin of Widespread Long-lived Volcanism Across the Galapagos Volcanic Province

Science.gov (United States)

O'Connor, J. M.; Stoffers, P.; Wijbrans, J. R.; Worthington, T. J.

2005-12-01

40Ar/39Ar ages for rocks dredged (SO144 PAGANINI expedition) and drilled (DSDP) from the Galapagos Volcanic Province (Cocos, Carnegie, Coiba and Malpelo aseismic ridges and associated seamounts) show evidence of 1) increasing age with distance from the Galapagos Archipelago, 2) long-lived episodic volcanism at many locations, and 3) broad overlapping regions of coeval volcanism. The widespread nature of synchronous volcanism across the Galapagos Volcanic Province (GVP) suggests a correspondingly large Galapagos hotspot melting anomaly (O'Connor et al., 2004). Development of the GVP via Cocos and Nazca plate migration and divergence over this broad melting anomaly would explain continued multiple phases of volcanism over millions of years following the initial onset of hotspot volcanism. The question arising from these observations is whether long-lived GVP episodic volcanism is equivalent to `rejuvenescent' or a `post-erosional' phase of volcanism that occurs hundreds of thousands or million years after the main shield-building phase documented on many mid-plate seamount chains, most notably along the Hawaiian-Emperor Seamount Chain? Thus, investigating the process responsible for long-lived episodic GVP volcanism provides the opportunity to evaluate this little understood process of rejuvenation in a physical setting very different to the Hawaiian-Emperor Chain (i.e. on/near spreading axis versus mid-plate). We consider here timing and geochemical information to test the various geodynamic models proposed to explain the origin of GVP hotspot volcanism, especially the possibility of rejuvenated phases that erupt long after initial shield-building.

Reactive Uptake of Sulfur Dioxide and Ozone on Volcanic Glass and Ash at Ambient Temperature

Science.gov (United States)

Maters, Elena C.; Delmelle, Pierre; Rossi, Michel J.; Ayris, Paul M.

2017-09-01

The atmospheric impacts of volcanic ash from explosive eruptions are rarely considered alongside those of volcanogenic gases/aerosols. While airborne particles provide solid surfaces for chemical reactions with trace gases in the atmosphere, the reactivity of airborne ash has seldom been investigated. Here we determine the total uptake capacity (NiM) and initial uptake coefficient (γM) for sulfur dioxide (SO2) and ozone (O3) on a compositional array of volcanic ash and glass powders at 25°C in a Knudsen flow reactor. The measured ranges of NiSO2 and γSO2 (1011-1013 molecules cm-2 and 10-3-10-2) and NiO3 and γO3 (1012-1013 molecules cm-2 and 10-3-10-2) are comparable to values reported for mineral dust. Differences in ash and glass reactivity toward SO2 and O3 may relate to varying abundances of, respectively, basic and reducing sites on these materials. The typically lower SO2 and O3 uptake on ash compared to glass likely results from prior exposure of ash surfaces to acidic and oxidizing conditions within the volcanic eruption plume/cloud. While sequential uptake experiments overall suggest that these gases do not compete for reactive surface sites, SO2 uptake forming adsorbed S(IV) species may enhance the capacity for subsequent O3 uptake via redox reaction forming adsorbed S(VI) species. Our findings imply that ash emissions may represent a hitherto neglected sink for atmospheric SO2 and O3.

NOVAC - Network for Observation of Volcanic and Atmospheric Change: Data archiving and management

Science.gov (United States)

Lehmann, T.; Kern, C.; Vogel, L.; Platt, U.; Johansson, M.; Galle, B.

2009-12-01

The potential for volcanic risk assessment using real-time gas emissions data and the recognized power of sharing data from multiple eruptive centers were the motivation for a European Union FP6 Research Program project entitled NOVAC: Network for Observation of Volcanic and Atmospheric Change. Starting in 2005, a worldwide network of permanent scanning Differential Optical Absorption Spectroscopy (DOAS) instruments was installed at 26 volcanoes around the world. These ground-based remote sensing instruments record the characteristic absorption of volcanic gas emissions (e.g. SO2, BrO) in the ultra-violet wavelength region. A real-time DOAS retrieval was implemented to evaluate the measured spectra, thus providing the respective observatories with gas emission data which can be used for volcanic risk assessment and hazard prediction. Observatory personnel at each partner institution were trained on technical and scientific aspects of the DOAS technique, and a central database was created to allow the exchange of data and ideas between all partners. A bilateral benefit for volcano observatories as well as scientific institutions (e.g. universities and research centers) resulted. Volcano observatories were provided with leading edge technology for measuring volcanic SO2 emission fluxes, and now use this technology for monitoring and risk assessment, while the involved universities and research centers are working on global studies and characterizing the atmospheric impact of the observed gas emissions. The NOVAC database takes into account that project members use the database in a variety of different ways. Therefore, the data is structured in layers, the top of which contains basic information about each instrument. The second layer contains evaluated emission data such as SO2 column densities, SO2 emission fluxes, and BrO/SO2 ratios. The lowest layer contains all spectra measured by the individual instruments. Online since the middle of 2006, the NOVAC database

Inventory of gas flux measurements from volcanoes of the global Network for Observation of Volcanic and Atmospheric Change (NOVAC)

Science.gov (United States)

Galle, B.; Arellano, S.; Norman, P.; Conde, V.

2012-04-01

NOVAC, the Network for Observation of Volcanic and Atmospheric Change, was initiated in 2005 as a 5-year-long project financed by the European Union. Its main purpose is to create a global network for the monitoring and research of volcanic atmospheric plumes and related geophysical phenomena by using state-of-the-art spectroscopic remote sensing technology. Up to 2012, 64 instruments have been installed at 24 volcanoes in 13 countries of Latin America, Italy, Democratic Republic of Congo, Reunion, Iceland, and Philippines, and efforts are being done to expand the network to other active volcanic zones. NOVAC has been a pioneer initiative in the community of volcanologists and embraces the objectives of the Word Organization of Volcano Observatories (WOVO) and the Global Earth Observation System of Systems (GEOSS). In this contribution, we present the results of the measurements of SO2 gas fluxes carried out within NOVAC, which for some volcanoes represent a record of more than 7 years of continuous monitoring. The network comprises some of the most strongly degassing volcanoes in the world, covering a broad range of tectonic settings, levels of unrest, and potential risk. We show a global perspective of the output of volcanic gas from the covered regions, specific trends of degassing for a few selected volcanoes, and the significance of the database for further studies in volcanology and other geosciences.

Model-based aviation advice on distal volcanic ash clouds by assimilating aircraft in situ measurements

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G. Fu

2016-07-01

Full Text Available The forecast accuracy of distal volcanic ash clouds is important for providing valid aviation advice during volcanic ash eruption. However, because the distal part of volcanic ash plume is far from the volcano, the influence of eruption information on this part becomes rather indirect and uncertain, resulting in inaccurate volcanic ash forecasts in these distal areas. In our approach, we use real-life aircraft in situ observations, measured in the northwestern part of Germany during the 2010 Eyjafjallajökull eruption, in an ensemble-based data assimilation system combined with a volcanic ash transport model to investigate the potential improvement on the forecast accuracy with regard to the distal volcanic ash plume. We show that the error of the analyzed volcanic ash state can be significantly reduced through assimilating real-life in situ measurements. After a continuous assimilation, it is shown that the aviation advice for Germany, the Netherlands and Luxembourg can be significantly improved. We suggest that with suitable aircrafts measuring once per day across the distal volcanic ash plume, the description and prediction of volcanic ash clouds in these areas can be greatly improved.

NO2 column changes induced by volcanic eruptions

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Johnston, Paul V.; Keys, J. Gordon; Mckenzie, Richard L.

1994-01-01

Nitrogen dioxide slant column amounts measured by ground-based remote sensing from Lauder, New Zealand (45 deg S) and Campbell Island (53 deg S) during the second half of 1991 and early 1992 show anomalously low values that are attributed to the effects of volcanic eruptions. It is believed that the eruptions of Mount Pinatubo in the Philippines in June 1991 and possibly Mount Hudson in Chile in August 1991 are responsible for the stratospheric changes, which first became apparent in July 1991. The effects in the spring of 1991 are manifested as a reduction in the retrieved NO2 column amounts from normal levels by 35 to 45 percent, and an accompanying increase in the overnight decay of NO2. The existence of an accurate long-term record of column NO2 from the Lauder site enables us to quantify departures from the normal seasonal behavior with some confidence. Simultaneous retrievals of column ozone agree well with Dobson measurements, confirming that only part of the NO2 changes can be attributed to a modification of the scattering geometry by volcanic aerosols. Other reasons for the observed behavior are explored, including the effects of stratospheric temperature increases resulting from the aerosol loading and the possible involvement of heterogeneous chemical processes.

Airborne multi-axis DOAS measurements of tropospheric SO2 plumes in the Po-valley, Italy

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P. Wang

2006-01-01

Full Text Available During the second FORMAT (FORMaldehyde as A Tracer of oxidation in the troposphere campaign in 2003 the airborne multi-axis DOAS instrument (AMAXDOAS performed scattered-light spectroscopic measurements of SO2 over the city of Mantova and the power plant Porto Tolle, both situated in the Po-valley, Northern Italy. The SO2 vertical columns and emission flux were derived from two days of measurements, 26 and 27 September 2003. The SO2 emission flux from the power plant Porto Tolle was calculated to 1.93×1025 molec s-1 on 26 September and in good agreement with official emission data, which quote 2.25×1025 molec s-1. On 27 September the measured flux was much lower (3.77×1024 molec s-1 if ECMWF wind data are used, but of comparable magnitude (2.4×1025 molec s-1 if the aircraft on-board wind measurements are utilised. Official emission data was 2.07×1025 molec s-1 indicating only a small change from the previous day. Over the city of Mantova, the observed SO2 vertical columns were 1.1×1016 molec cm-2 and 1.9×1016 molec cm-2 on 26 and 27 September, respectively. This is in good agreement with ground-based measurements of 5.9 ppbv and 10.0 ppbv which correspond to 1.2×1016 molec cm-2 and 2.2×1016 molec cm-2 if a well mixed boundary layer of 500m altitude is assumed.

[Effects of volcanic eruptions on environment and health].

Science.gov (United States)

Zuskin, Eugenija; Mustajbegović, Jadranka; Doko Jelinić, Jagoda; Pucarin-Cvetković, Jasna; Milosević, Milan

2007-12-01

Volcanoes pose a threat to almost half a billion people; today there are approximately 500 active volcanoes on Earth, and every year there are 10 to 40 volcanic eruptions. Volcanic eruptions produce hazardous effects for the environment, climate, and the health of the exposed persons, and are associated with the deterioration of social and economic conditions. Along with magma and steam (H2O), the following gases surface in the environment: carbon dioxide (CO2) and sulphur dioxide (SO2), carbon monoxide (CO), hydrogen sulphide (H2S), carbon sulphide (CS), carbon disulfide (CS2), hydrogen chloride (HCl), hydrogen (H2), methane (CH4), hydrogen fluoride (HF), hydrogen bromide (HBr) and various organic compounds, as well as heavy metals (mercury, lead, gold).Their unfavourable effects depend on the distance from a volcano, on magma viscosity, and on gas concentrations. The hazards closer to the volcano include pyroclastic flows, flows of mud, gases and steam, earthquakes, blasts of air, and tsunamis. Among the hazards in distant areas are the effects of toxic volcanic ashes and problems of the respiratory system, eyes and skin, as well as psychological effects, injuries, transport and communication problems, waste disposal and water supplies issues, collapse of buildings and power outage. Further effects are the deterioration of water quality, fewer periods of rain, crop damages, and the destruction of vegetation. During volcanic eruptions and their immediate aftermath, increased respiratory system morbidity has been observed as well as mortality among those affected by volcanic eruptions. Unfavourable health effects could partly be prevented by timely application of safety measures.

Validating the accuracy of SO2 gas retrievals in the thermal infrared (8-14 μm)

Science.gov (United States)

Gabrieli, Andrea; Porter, John N.; Wright, Robert; Lucey, Paul G.

2017-11-01

Quantifying sulfur dioxide (SO2) in volcanic plumes is important for eruption predictions and public health. Ground-based remote sensing of spectral radiance of plumes contains information on the path-concentration of SO2. However, reliable inversion algorithms are needed to convert plume spectral radiance measurements into SO2 path-concentrations. Various techniques have been used for this purpose. Recent approaches have employed thermal infrared (TIR) imaging between 8 μm and 14 μm to provide two-dimensional mapping of plume SO2 path-concentration, using what might be described as "dual-view" techniques. In this case, the radiance (or its surrogate brightness temperature) is computed for portions of the image that correspond to the plume and compared with spectral radiance obtained for adjacent regions of the image that do not (i.e., "clear sky"). In this way, the contribution that the plume makes to the measured radiance can be isolated from the background atmospheric contribution, this residual signal being converted to an estimate of gas path-concentration via radiative transfer modeling. These dual-view approaches suffer from several issues, mainly the assumption of clear sky background conditions. At this time, the various inversion algorithms remain poorly validated. This paper makes two contributions. Firstly, it validates the aforementioned dual-view approaches, using hyperspectral TIR imaging data. Secondly, it introduces a new method to derive SO2 path-concentrations, which allows for single point SO2 path-concentration retrievals, suitable for hyperspectral imaging with clear or cloudy background conditions. The SO2 amenable lookup table algorithm (SO2-ALTA) uses the MODTRAN5 radiative transfer model to compute radiance for a variety (millions) of plume and atmospheric conditions. Rather than searching this lookup table to find the best fit for each measured spectrum, the lookup table was used to train a partial least square regression (PLSR) model

Summit CO2 emission rates by the CO2/SO2 ratio method at Kīlauea Volcano, Hawaiʻi, during a period of sustained inflation

Science.gov (United States)

Hager, S.A.; Gerlach, T.M.; Wallace, P.J.

2008-01-01

The emission rate of carbon dioxide escaping from the summit of Kīlauea Volcano, Hawaiʻi, proved highly variable, averaging 4900 ± 2000 metric tons per day (t/d) in June–July 2003 during a period of summit inflation. These results were obtained by combining over 90 measurements of COSPEC-derived SO2emission rates with synchronous CO2/SO2 ratios of the volcanic gas plume along the summit COSPEC traverse. The results are lower than the CO2 emission rate of 8500 ± 300 t/d measured by the same method in 1995–1999 during a period of long-term summit deflation [Gerlach, T.M., McGee, K.A., Elias, T., Sutton, A.J. and Doukas, M.P., 2002. Carbon dioxide emission rate of Kīlauea Volcano: Implications for primary magma and the summit reservoir. Journal of Geophysical Research-Solid Earth, 107(B9): art. no.-2189.]. Analysis of the data indicates that the emission rates of the present study likely reflect changes in the magma supply rate and residence time in the summit reservoir. It is also likely that emission rates during the inflation period were heavily influenced by SO2 pulses emitted adjacent to the COSPEC traverse, which biased CO2/SO2 ratios towards low values that may be unrepresentative of the global summit gas plume. We conclude that the SO2 pulses are consequences of summit re-inflation under way since 2003 and that CO2 emission rates remain comparable to, but more variable than, those measured prior to re-inflation.

Volcanogenic SO2, a natural pollutant: Measurements, modeling and hazard assessment at Vulcano Island (Aeolian Archipelago, Italy).

Science.gov (United States)

Granieri, Domenico; Vita, Fabio; Inguaggiato, Salvatore

2017-12-01

Sulfur dioxide (SO 2 ) is a major component of magmatic gas discharges. Once emitted in the atmosphere it can affect the air and land environment at different spatial and temporal scales, with harmful effects on human health and plant communities. We used a dense dataset of continuous SO 2 flux and meteorological measurements collected at Vulcano over an 8-year period spanning from May 2008 to February 2016 to model air SO 2 concentrations over the island. To this end, we adopted the DISGAS (DISpersion of GAS) numerical code coupled with the Diagnostic Wind Model (DWM). SO 2 concentrations in air were determined for three different SO 2 emission rates: a reference SO 2 flux of ∼18 t/d (the median of more than 800 measurements), an enhanced SO 2 flux of 40 t/d (average of all measurements plus 1 σ), and a maximum SO 2 flux of 106 t/d (maximum value measured in the investigated period). Maximum SO 2 concentrations in air were estimated at the crater, near the high-T fumarole field that is the source of the gas, and ranged from 2000 ppb to ∼24,000 ppb for the reference flux, from 2000 ppb to 51,000 ppb for the enhanced flux and from 5000 ppb to 136,000 ppb for the maximum flux, with peak values in limited areas at the bottom of the crater. These concentrations pose a hazard for people visiting the crater, for sensitive individuals in particular. Based on estimated SO 2 concentrations in air, we also consider the phytotoxic effects of SO 2 on local vegetation. Copyright © 2017 Elsevier Ltd. All rights reserved.

Soil CO2 efflux measurement network by means of closed static chambers to monitor volcanic activity at Tenerife, Canary Islands

Science.gov (United States)

Amonte, Cecilia; García-Merino, Marta; Asensio-Ramos, María; Melián, Gladys; García-Hernández, Rubén; Pérez, Aaron; Hernández, Pedro A.; Pérez, Nemesio M.

2017-04-01

Tenerife (2304 km2) is the largest of the Canary Islands and has developed a central volcanic complex (Cañadas edifice), that started to grow about 3.5 My ago. Coeval with the construction of the Cañadas edifice, shield basaltic volcanism continued until the present along three rift zones oriented NW-SE, NE-SW and NS (hereinafter referred as NW, NE and NS respectively). Main volcanic historical activity has occurred along de NW and NE rift-zones, although summit cone of Teide volcano, in central volcanic complex, is the only area of the island where surface geothermal manifestations are visible. Uprising of deep-seated gases occurs along the aforementioned volcanic structures causing diffuse emissions at the surface environment of the rift-zones. In the last 20 years, there has been considerable interest in the study of diffuse degassing as a powerful tool in volcano monitoring programs. Diffuse degassing studies are even more important volcanic surveillance tool at those volcanic areas where visible manifestations of volcanic gases are absent. Historically, soil gas and diffuse degassing surveys in volcanic environments have focused mainly on CO2 because it is, after water vapor, the most abundant gas dissolved in magma. One of the most popular methods used to determine CO2 fluxes in soil sciences is based on the absorption of CO2 through an alkaline medium, in its solid or liquid form, followed by gravimetric, conductivity, or titration analyses. In the summer of 2016, a network of 31 closed static chambers was installed, covering the three main structural zones of Tenerife (NE, NW and NS) as well as Cañadas Caldera with volcanic surveillance porpoises. 50 cc of 0.1N KOH solution is placed inside the chamber to absorb the CO2 released from the soil. The solution is replaced weekly and the trapped CO2 is then analyzed at the laboratory by titration. The are expressed as weekly integrated CO2 efflux values. The CO2 efflux values ranged from 3.2 to 12.9 gṡm-2�

Observation of the volcanic plume of Eyjafjallajoekull over continental Europe by MAX-DOAS

Energy Technology Data Exchange (ETDEWEB)

Yilmaz, S.; Bobrowski, N.; Friess, U.; Platt, U. [IUP, University of Heidelberg (Germany); Flentje, H. [DWD, Hohenpeissenberg (Germany); Hoermann, C.; Sihler, H. [IUP, University of Heidelberg (Germany); MPI, Mainz (Germany); Kern, C. [USGS, Vancouver (Canada); Wagner, T. [MPI, Mainz (Germany)

2011-07-01

The recent eruption of Eyjafjallajoekull Volcano (Iceland) and the emitted ash plume which disrupted commercial air traffic over Europe has led to an exhaustive debate on how to improve our ability to quantitatively determine the ash load in the atmosphere as a function of time and geographical location. Satellite instruments detecting ash and SO{sub 2} and ground-based LIDAR stations can help constrain atmospheric transport and meteorology models used to predict ash dispersion. However, MAX-DOAS represents an additional tool with considerable potential for the quantitative detection of elevated volcanic ash and SO{sub 2} plumes. It performs especially well during weather conditions in which satellites and LIDARs are impeded in their effectiveness, e.g. in the case of dense clouds above or below the plume, respectively. Here, the advantages and disadvantages of the DOAS technique are discussed, and its potential for monitoring of volcanic ash hazards explored. Results of ash and SO{sub 2} measurements of the Eyjafjallajoekull plume as it passed over Heidelberg are presented as an example of a positive detection of a highly diluted volcanic plume. Their low cost and complementary nature makes MAX-DOAS a promising technology in the field of aviation hazard detection and management.

Reference dataset of volcanic ash physicochemical and optical properties for atmospheric measurement retrievals and transport modelling

Science.gov (United States)

Vogel, Andreas; Durant, Adam; Sytchkova, Anna; Diplas, Spyros; Bonadonna, Costanza; Scarnato, Barbara; Krüger, Kirstin; Kylling, Arve; Kristiansen, Nina; Stohl, Andreas

2016-04-01

Explosive volcanic eruptions emit up to 50 wt.% (total erupted mass) of fine ash particles (estimates of the volcanic source term and the nature of the constituent volcanic ash properties. Consequently, it is important to include a quantitative assessment of measurement uncertainties of ash properties to provide realistic ash forecast uncertainty. Currently, information on volcanic ash physicochemical and optical properties is derived from a small number of somewhat dated publications. In this study, we provide a reference dataset for physical (size distribution and shape), chemical (bulk vs. surface chemistry) and optical properties (complex refractive index in the UV-vis-NIR range) of a representative selection of volcanic ash samples from 10 different volcanic eruptions covering the full variability in silica content (40-75 wt.% SiO2). Through the combination of empirical analytical methods (e.g., image analysis, Energy Dispersive Spectroscopy, X-ray Photoelectron Spectroscopy, Transmission Electron Microscopy and UV/Vis/NIR/FTIR Spectroscopy) and theoretical models (e.g., Bruggeman effective medium approach), it was possible to fully capture the natural variability of ash physicochemical and optical characteristics. The dataset will be applied in atmospheric measurement retrievals and atmospheric transport modelling to determine the sensitivity to uncertainty in ash particle characteristics.

Ground-Based Remote Sensing of Volcanic CO2 Fluxes at Solfatara (Italy—Direct Versus Inverse Bayesian Retrieval

Directory of Open Access Journals (Sweden)

Manuel Queißer

2018-01-01

Full Text Available CO2 is the second most abundant volatile species of degassing magma. CO2 fluxes carry information of incredible value, such as periods of volcanic unrest. Ground-based laser remote sensing is a powerful technique to measure CO2 fluxes in a spatially integrated manner, quickly and from a safe distance, but it needs accurate knowledge of the plume speed. The latter is often difficult to estimate, particularly for complex topographies. So, a supplementary or even alternative way of retrieving fluxes would be beneficial. Here, we assess Bayesian inversion as a potential technique for the case of the volcanic crater of Solfatara (Italy, a complex terrain hosting two major CO2 degassing fumarolic vents close to a steep slope. Direct integration of remotely sensed CO2 concentrations of these vents using plume speed derived from optical flow analysis yielded a flux of 717 ± 121 t day−1, in agreement with independent measurements. The flux from Bayesian inversion based on a simple Gaussian plume model was in excellent agreement under certain conditions. In conclusion, Bayesian inversion is a promising retrieval tool for CO2 fluxes, especially in situations where plume speed estimation methods fail, e.g., optical flow for transparent plumes. The results have implications beyond volcanology, including ground-based remote sensing of greenhouse gases and verification of satellite soundings.

First results of the Piton de la Fournaise STRAP 2015 experiment: multidisciplinary tracking of a volcanic gas and aerosol plume

Science.gov (United States)

Tulet, Pierre; Di Muro, Andréa; Colomb, Aurélie; Denjean, Cyrielle; Duflot, Valentin; Arellano, Santiago; Foucart, Brice; Brioude, Jérome; Sellegri, Karine; Peltier, Aline; Aiuppa, Alessandro; Barthe, Christelle; Bhugwant, Chatrapatty; Bielli, Soline; Boissier, Patrice; Boudoire, Guillaume; Bourrianne, Thierry; Brunet, Christophe; Burnet, Fréderic; Cammas, Jean-Pierre; Gabarrot, Franck; Galle, Bo; Giudice, Gaetano; Guadagno, Christian; Jeamblu, Fréderic; Kowalski, Philippe; Leclair de Bellevue, Jimmy; Marquestaut, Nicolas; Mékies, Dominique; Metzger, Jean-Marc; Pianezze, Joris; Portafaix, Thierry; Sciare, Jean; Tournigand, Arnaud; Villeneuve, Nicolas

2017-04-01

The STRAP (Synergie Transdisciplinaire pour Répondre aux Aléas liés aux Panaches volcaniques) campaign was conducted over the entire year of 2015 to investigate the volcanic plumes of Piton de La Fournaise (La Réunion, France). For the first time, measurements at the local (near the vent) and at the regional scales were conducted around the island. The STRAP 2015 campaign has become possible thanks to strong cross-disciplinary collaboration between volcanologists and meteorologists. The main observations during four eruptive periods (85 days) are summarised. They include the estimates of SO2, CO2 and H2O emissions, the altitude of the plume at the vent and over different areas of La Réunion Island, the evolution of the SO2 concentration, the aerosol size distribution and the aerosol extinction profile. A climatology of the volcanic plume dispersion is also reported. Simulations and measurements show that the plumes formed by weak eruptions have a stronger interaction with the surface of the island. Strong SO2 mixing ratio and particle concentrations above 1000 ppb and 50 000 cm-3 respectively are frequently measured over a distance of 20 km from Piton de la Fournaise. The measured aerosol size distribution shows the predominance of small particles in the volcanic plume. Several cases of strong nucleation of sulfuric acid have been observed within the plume and at the distal site of the Maïdo observatory. The STRAP 2015 campaign provides a unique set of multi-disciplinary data that can now be used by modellers to improve the numerical parameterisations of the physical and chemical evolution of the volcanic plumes.

Rate constant for the reaction SO + BrO yields SO2 + Br

Science.gov (United States)

Brunning, J.; Stief, L.

1986-01-01

The rate of the radical-radical reaction SO + BrO yields SO2 + Br has been determined at 298 K in a discharge flow system near 1 torr pressure with detection of SO and BrO via collision-free sampling mass spectrometry. The rate constant was determined using two different methods: measuring the decay of SO radicals in the presence of an excess of BrO and measuring the decay of BrO radicals in excess SO. The results from the two methods are in reasonable agreement and the simple mean of the two values gives the recommended rate constant at 298 K, k = (5.7 + or - 2.0) x 10 to the -11th cu cm/s. This represents the first determination of this rate constant and it is consistent with a previously derived lower limit based on SO2 formation. Comparison is made with other radical-radical reactions involving SO or BrO. The reaction SO + BrO yields SO2 + Br is of interest for models of the upper atmosphere of the earth and provides a potential coupling between atmospheric sulfur and bromine chemistry.

SO2 photoexcitation mechanism links mass-independent sulfur isotopic fractionation in cryospheric sulfate to climate impacting volcanism

DEFF Research Database (Denmark)

Hattori, Shohei; Schmidt, Johan Albrecht; Johnson, Matthew Stanley

2013-01-01

Natural climate variation, such as that caused by volcanoes, is the basis for identifying anthropogenic climate change. However, knowledge of the history of volcanic activity is inadequate, particularly concerning the explosivity of specific events. Some material is deposited in ice cores......, but the concentration of glacial sulfate does not distinguish between tropospheric and stratospheric eruptions. Stable sulfur isotope abundances contain additional information, and recent studies show a correlation between volcanic plumes that reach the stratosphere and mass-independent anomalies in sulfur isotopes...... plume chemistry, allowing the production and preservation of a mass-independent sulfur isotope anomaly in the sulfate product. The model accounts for the amplitude, phases, and time development of Δ(33)S/δ(34)S and Δ(36)S/Δ(33)S found in glacial samples. We are able to identify the process controlling...

Increased Atmospheric SO2 Detected from Changes in Leaf Physiognomy across the Triassic–Jurassic Boundary Interval of East Greenland

Science.gov (United States)

Bacon, Karen L.; Belcher, Claire M.; Haworth, Matthew; McElwain, Jennifer C.

2013-01-01

The Triassic–Jurassic boundary (Tr–J; ∼201 Ma) is marked by a doubling in the concentration of atmospheric CO2, rising temperatures, and ecosystem instability. This appears to have been driven by a major perturbation in the global carbon cycle due to massive volcanism in the Central Atlantic Magmatic Province. It is hypothesized that this volcanism also likely delivered sulphur dioxide (SO2) to the atmosphere. The role that SO2 may have played in leading to ecosystem instability at the time has not received much attention. To date, little direct evidence has been presented from the fossil record capable of implicating SO2 as a cause of plant extinctions at this time. In order to address this, we performed a physiognomic leaf analysis on well-preserved fossil leaves, including Ginkgoales, bennettites, and conifers from nine plant beds that span the Tr–J boundary at Astartekløft, East Greenland. The physiognomic responses of fossil taxa were compared to the leaf size and shape variations observed in nearest living equivalent taxa exposed to simulated palaeoatmospheric treatments in controlled environment chambers. The modern taxa showed a statistically significant increase in leaf roundness when fumigated with SO2. A similar increase in leaf roundness was also observed in the Tr–J fossil taxa immediately prior to a sudden decrease in their relative abundances at Astartekløft. This research reveals that increases in atmospheric SO2 can likely be traced in the fossil record by analyzing physiognomic changes in fossil leaves. A pattern of relative abundance decline following increased leaf roundness for all six fossil taxa investigated supports the hypothesis that SO2 had a significant role in Tr–J plant extinctions. This finding highlights that the role of SO2 in plant biodiversity declines across other major geological boundaries coinciding with global scale volcanism should be further explored using leaf physiognomy. PMID:23593262

Timing and climate forcing of volcanic eruptions for the past 2,500 years.

Science.gov (United States)

Sigl, M; Winstrup, M; McConnell, J R; Welten, K C; Plunkett, G; Ludlow, F; Büntgen, U; Caffee, M; Chellman, N; Dahl-Jensen, D; Fischer, H; Kipfstuhl, S; Kostick, C; Maselli, O J; Mekhaldi, F; Mulvaney, R; Muscheler, R; Pasteris, D R; Pilcher, J R; Salzer, M; Schüpbach, S; Steffensen, J P; Vinther, B M; Woodruff, T E

2015-07-30

Volcanic eruptions contribute to climate variability, but quantifying these contributions has been limited by inconsistencies in the timing of atmospheric volcanic aerosol loading determined from ice cores and subsequent cooling from climate proxies such as tree rings. Here we resolve these inconsistencies and show that large eruptions in the tropics and high latitudes were primary drivers of interannual-to-decadal temperature variability in the Northern Hemisphere during the past 2,500 years. Our results are based on new records of atmospheric aerosol loading developed from high-resolution, multi-parameter measurements from an array of Greenland and Antarctic ice cores as well as distinctive age markers to constrain chronologies. Overall, cooling was proportional to the magnitude of volcanic forcing and persisted for up to ten years after some of the largest eruptive episodes. Our revised timescale more firmly implicates volcanic eruptions as catalysts in the major sixth-century pandemics, famines, and socioeconomic disruptions in Eurasia and Mesoamerica while allowing multi-millennium quantification of climate response to volcanic forcing.

Structural control of monogenetic volcanism in the Garrotxa volcanic field (Northeastern Spain) from gravity and self-potential measurements

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Barde-Cabusson, S.; Gottsmann, J.; Martí, J.; Bolós, X.; Camacho, A. G.; Geyer, A.; Planagumà, Ll.; Ronchin, E.; Sánchez, A.

2014-01-01

We report new geophysical observations on the distribution of subsurface structures associated with monogenetic volcanism in the Garrotxa volcanic field (Northern Spain). As part of the Catalan Volcanic Zone, this Quaternary volcanic field is associated with the European rifts system. It contains the most recent and best preserved volcanic edifices of the Catalan Volcanic Zone with 38 monogenetic volcanoes identified in the Garrotxa Natural Park. We conducted new gravimetric and self-potential surveys to enhance our understanding of the relationship between the local geology and the spatial distribution of the monogenetic volcanoes. The main finding of this study is that the central part of the volcanic field is dominated by a broad negative Bouguer anomaly of around -0.5 mGal, within which a series of gravity minima are found with amplitudes of up to -2.3 mGal. Inverse modelling of the Bouguer data suggests that surficial low-density material dominates the volcanic field, most likely associated with effusive and explosive surface deposits. In contrast, an arcuate cluster of gravity minima to the NW of the Croscat volcano, the youngest volcano of this zone, is modelled by vertically extended low-density bodies, which we interpret as a complex ensemble of fault damage zones and the roots of young scoria cones. A ground-water infiltration zone identified by a self-potential anomaly is associated with a steep horizontal Bouguer gravity gradient and interpreted as a fault zone and/or magmatic fissure, which fed the most recent volcanic activity in the Garrotxa. Gravimetric and self-potential data are well correlated and indicate a control on the locations of scoria cones by NNE-SSW and NNW-SSE striking tectonic features, which intersect the main structural boundaries of the study area to the north and south. Our interpretation of the data is that faults facilitated magma ascent to the surface. Our findings have major implications for understanding the relationship

Measurement of CO{sub 2}, CO, SO{sub 2}, and NO emissions from coal-based thermal power plants in India

Energy Technology Data Exchange (ETDEWEB)

Chakraborty, N.; Mukheriee, I.; Santra, A.K.; Chowdhury, S.; Chakraborty, S.; Bhattacharya, S.; Mitra, A.P.; Sharma, C. [Jadavpur University, Calcutta (India). Dept. of Power Engineering

2008-02-15

Measurements of CO{sub 2} (direct GHG) and CO, SO{sub 2}, NO (indirect GHGs) were conducted on-line at some of the coal-based thermal power plants in India. The objective of the study was three-fold: to quantify the measured emissions in terms of emission coefficient per kg of coal and per kWh of electricity, to calculate the total possible emission from Indian thermal power plants, and subsequently to compare them with some previous studies. Instrument IMR 2800P Flue Gas Analyzer was used on-line to measure the emission rates Of CO{sub 2}, CO, SO{sub 2}, and NO at 11 numbers of generating units of different ratings. Certain quality assurance (QA) and quality control (QC) techniques were also adopted to gather the data so as to avoid any ambiguity in subsequent data interpretation. For the betterment of data interpretation, the requisite statistical parameters (standard deviation and arithmetic mean) for the measured emissions have been also calculated. The emission coefficients determined for CO{sub 2}, CO, SO{sub 2}, and NO have been compared with their corresponding values as obtained in the studies conducted by other groups. The total emissions of CO{sub 2}, CO, SO{sub 2}, and NO calculated on the basis of the emission coefficients for the year 2003-2004 have been found to be 465.667, 1.583, 4.058, and 1.129 Tg, respectively.

Airborne emission measurements of SO2, NOx and particles from individual ships using sniffer technique

Science.gov (United States)

Beecken, J.; Mellqvist, J.; Salo, K.; Ekholm, J.; Jalkanen, J.-P.

2013-12-01

A dedicated system for airborne ship emission measurements of SO2, NOx and particles has been developed and used from several small aircrafts. The system has been adapted for fast response measurements at 1 Hz and the use of several of the instruments is unique. The uncertainty of the given data is about 20.3% for SO2 and 23.8% for NOx emission factors. Multiple measurements of 158 ships measured from the air on the Baltic and North Sea during 2011 and 2012 show emission factors of 18.8 ± 6.5 g kgfuel-1, 66.6 ± 23.4 g kgfuel-1, and 1.8 ± 1.3 × 1016 particles kgfuel-1 for SO2, NOx and particle number respectively. The particle size distributions were measured for particle diameters between 15 and 560 nm. The mean sizes of the particles are between 50 and 62 nm dependent on the distance to the source and the number size distribution is mono-modal. Concerning the sulfur fuel content 85% of the ships comply with the IMO limits. The sulfur emission has decreased compared to earlier measurements from 2007 to 2009. The presented method can be implemented for regular ship compliance monitoring.

Radiative effects of the El Chichon volcanic eruption. Preliminary results concerning remote sensing

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Bandeen, W. R.; Fraser, R. S.

1982-01-01

The aerosols and gases resulting from the El Chichon volcanic eruption had, and may still have, significant effects on satellite measurements of the properties of the Earth's atmosphere. The sea surface temperature measured by the AVHRR was biased up to -2.5 C for many months. The total amount of ozone derived from TOMS with a standard algorithm was greatly in excess of the possible value. This apparent excess can now be explained in terms of additional absorption by SO2. Infrared temperature sounders have observed both positive and negative anomalies. These effects and others on many satellite measurements are addressed following a discussion of the history and composition of the ejecta remaining in the stratosphere. Finally, recommendations are made for further study to account for the effects of volcanic eruptions on satellite observations and for use of such observations to measure the characteristics of the ejecta.

Emission of gas and atmospheric dispersion of SO2 during the December 2013 eruption at San Miguel volcano (El Salvador)

Science.gov (United States)

Salerno, Giuseppe G.; Granieri, Domenico; Liuzzo, Marco; La Spina, Alessandro; Giuffrida, Giovanni B.; Caltabiano, Tommaso; Giudice, Gaetano; Gutierrez, Eduardo; Montalvo, Francisco; Burton, Michael; Papale, Paolo

2016-04-01

y Recursos Naturales (MARN) of El Salvador and by a network of geophysical and geochemical stations established on the volcano by the Italian Istituto Nazionale di Geofisica e Vulcanologia (INGV), immediately after the December 2013 eruption, on the request of MARN. During the eruption, SO2 emissions increased from a background level of ~330 t d-1 to 2200 t d-1, dropping after the eruption to an average level of 680 t d-1. Wind measurements and SO2 fluxes during the pre-, syn- and post-eruptive stages were used to model SO2 dispersion around the volcano. Air SO2 concentration exceeds the dangerous threshold of 5 ppm in the crater region, and in some middle sectors of the highly visited volcanic cone.

VolcLab: A balloon-borne instrument package to measure ash, gas, electrical, and turbulence properties of volcanic plumes

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Airey, Martin; Harrison, Giles; Nicoll, Keri; Williams, Paul; Marlton, Graeme

2017-04-01

Release of volcanic ash into the atmosphere poses a significant hazard to air traffic. Exposure to appreciable concentrations (≥4 mg m-3) of ash can result in engine shutdown, air data system loss, and airframe damage, with sustained lower concentrations potentially causing other long-term detrimental effects [1]. Disruption to flights also has a societal impact. For example, the closure of European airspace following the 2010 eruption of Eyjafjallajökull resulted in global airline industry losses of order £1100 million daily and disruption to 10 million passengers. Accurate and effective measurement of the mass of ash in a volcanic plume along with in situ characterisation of other plume properties such as charge, turbulence, and SO2 concentration can be used in combination with plume dispersion modelling, remote sensing, and more sophisticated flight ban thresholds to mitigate the impact of future events. VolcLab is a disposable instrument package that may be attached to a standard commercial radiosonde, for rapid emergency deployment on a weather balloon platform. The payload includes a newly developed gravimetric sensor using the oscillating microbalance principle to measure mass directly without assumptions about particles' optical properties. The package also includes an SO2 gas detector, an optical sensor to detect ash and cloud backscatter from an LED source [2], a charge sensor to characterise electrical properties of the plume [3], and an accelerometer to measure in-plume turbulence [4]. VolcLab uses the established PANDORA interface [5], to provide data exchange and power from the radiosonde. In addition to the VolcLab measurements, the radiosonde provides standard meteorological data of temperature, pressure, and relative humidity, and GPS location. There are several benefits of using this instrument suite in this design and of using this method of deployment. Firstly, this is an all-in-one device requiring minimal expertise on the part of the end

In-Situ Detection of SO2 Plumes in Costa Rica from Turrialba Volcano using Balloon-borne Sondes

Science.gov (United States)

Diaz, J. A.; Selkirk, H. B.; Morris, G. A.; Krotkov, N. A.; Pieri, D. C.; Corrales, E.

2012-12-01

The Turrialba Volcano near San Jose, Costa Rica regularly emits plumes containing SO2. These plumes have been detected by the Ozone Monitoring Instrument (OMI), and evidence of these plumes has also appeared in the in-situ Ticosonde project record: a continuous balloon-borne ozonesonde launch experiment conducted in a weekly basis in Costa Rica. In the case of the latter, the interference reaction of SO2 in the cathode cell of the standard electrochemical concentration cell (ECC) ozonesonde results in apparent "notches" in the ozone profile at the altitudes of the plume. In this paper, we present an overview of the Ticosonde observations and correlate the appearance of the notches with air mass back trajectory calculations that link the profiles features to emissions from the volcano. In addition, during February 2012, we deployed the dual O3/SO2 sonde from the University of Costa Rica and detected a plume of SO2 linked by back trajectory calcluations to Turrialba as well as an urban plume resulting from diesel exhaust in the boundary layer. The integrated column SO2 from the sonde profile data agree well with the OMI overpass data for this event. Data from a tethersonde measurement two days prior to the dual sonde reveal concentrations at the ppm level at the volcanic source.

A Comparison of MODIS and DOAS Sulfur Dioxide Measurements of the April 24, 2004 Eruption of Anatahan Volcano, Mariana Islands

Science.gov (United States)

Meier, V. L.; Scuderi, L.; Fischer, T.; Realmuto, V.; Hilton, D.

2006-12-01

Measurements of volcanic SO2 emissions provide insight into the processes working below a volcano, which can presage volcanic events. Being able to measure SO2 in near real-time is invaluable for the planning and response of hazard mitigation teams. Currently, there are several methods used to quantify the SO2 output of degassing volcanoes. Ground and aerial-based measurements using the differential optical absorption spectrometer (mini-DOAS) provide real-time estimates of SO2 output. Satellite-based measurements, which can provide similar estimates in near real-time, have increasingly been used as a tool for volcanic monitoring. Direct Broadcast (DB) real-time processing of remotely sensed data from NASA's Earth Observing System (EOS) satellites (MODIS Terra and Aqua) presents volcanologists with a range of spectral bands and processing options for the study of volcanic emissions. While the spatial resolution of MODIS is 1 km in the Very Near Infrared (VNIR) and Thermal Infrared (TIR), a high temporal resolution and a wide range of radiance measurements in 32 channels between VNIR and TIR combine to provide a versatile space borne platform to monitor SO2 emissions from volcanoes. An important question remaining to be answered is how well do MODIS SO2 estimates compare with DOAS estimates? In 2004 ground-based plume measurements were collected on April 24th and 25th at Anatahan volcano in the Mariana Islands using a mini-DOAS (Fischer and Hilton). SO2 measurements for these same dates have also been calculated using MODIS images and SO2 mapping software (Realmuto). A comparison of these different approaches to the measurement of SO2 for the same plume is presented. Differences in these observations are used to better quantify SO2 emissions, to assess the current mismatch between ground based and remotely sensed retrievals, and to develop an approach to continuously and accurately monitor volcanic activity from space in near real-time.

The Dilemmas of Risk-Sensitive Development on a Small Volcanic Island

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Emily Wilkinson

2016-06-01

Full Text Available In the Small Islands Developing State (SIDS of St Vincent and the Grenadines in the Caribbean, the most destructive disasters in terms of human casualties have been the multiple eruptions of La Soufrière volcano situated in the north of St Vincent. Despite this major threat, people continue to live close to the volcano and national development plans do not include risk reduction measures for volcanic hazards. This paper examines the development options in volcanic SIDS and presents a number of conundrums for disaster risk management on the island of St Vincent. Improvements in monitoring of volcanic hazards and ongoing programmes to enhance communications systems and encourage community preparedness planning have increased awareness of the risks associated with volcanic hazards, yet this has not translated into more risk-informed development planning decisions. The current physical development plan in fact promotes investment in infrastructure in settlements located within the zone designated very high-hazard. However, this is not an anomaly or an irrational decision: severe space constraints in SIDS, as well as other historical social and economic factors, limit growth and options for low-risk development. Greater attention needs to be placed on developing measures to reduce risk, particularly from low-intensity hazards like ash, limiting where possible exposure to volcanic hazards and building the resilience of communities living in high-risk areas. This requires planning for both short- and longer-term impacts from renewed activity. Volcanic SIDS face multiple hazards because of their geography and topography, so development plans should identify these interconnected risks and options for their reduction, alongside measures aimed at improving personal preparedness plans so communities can learn to live with risk.

Overview of gas flux measurements from volcanoes of the global Network for Observation of Volcanic and Atmospheric Change (NOVAC)

Science.gov (United States)

Galle, Bo; Arellano, Santiago; Conde, Vladimir

2015-04-01

NOVAC, the Network for Observation of Volcanic and Atmospheric Change, was initiated in 2005 as a 5-years-long project financed by the European Union. Its main purpose is to create a global network for the study of volcanic atmospheric plumes and related geophysical phenomena by using state-of-the-art spectroscopic remote sensing technology. Up to 2014, 67 instruments have been installed at 25 volcanoes in 13 countries of Latin America, Italy, Democratic Republic of Congo, Reunion, Iceland, and Philippines, and efforts are being done to expand the network to other active volcanic zones. NOVAC has been a pioneer initiative in the community of volcanologists and embraces the objectives of the Word Organization of Volcano Observatories (WOVO) and the Global Earth Observation System of Systems (GEOSS). In this contribution, we present the results of the measurements of SO2 gas fluxes carried out within NOVAC, which for some volcanoes represent a record of more than 8 years of semi-continuous monitoring. The network comprises some of the most strongly degassing volcanoes in the world, covering a broad range of tectonic settings, levels of unrest, and potential risk. Examples of correlations with seismicity and other geophysical phenomena, environmental impact studies and comparisons with previous global estimates will be discussed as well as the significance of the database for further studies in volcanology and other geosciences.

Ground based measurements of SO2 and NO2 emissions from the oil refinery 'la Teja' in Montevideo city

International Nuclear Information System (INIS)

Frins, Erna; Casaballe, Nicolas; Osorio, Matias; Arismendi, Federico; Ibrahim, Ossama; Wagner, Thomas; Platt, Ulrich

2011-01-01

We present preliminary results of ground based measurements of SO 2 and NO 2 emissions from 'La Teja' oil refinery located in the northern part of Montevideo Bay. Our study is part of a long term effort to localize and monitor relevant emission sources in the city area of Montevideo. These measurements were performed with a Miniature Multi AXis Differential Optical Absorption Spectrometry (MiniMAX-DOAS) instrument, which is basically a temperature controlled medium-resolution spectrometer (∼ 0.5 nm) equipped with a small telescope and a stepper motor allowing automatic scans in one dimension. We present a discussion about the evolution and transformation of both above species in the atmosphere. Our observation site was approximately 1.9 km away from the oil refinery and we were able to perform vertical and horizontal scans of the plume emitted (during our measurements) almost horizontally from its stacks. The maximum value of the SO 2 slant column density (SCD) was found to be ∼ 4x10 17 molec cm -2 directly over the oil refinery, decreasing as the plume disperses. In contrast, the NO 2 SCD peaks at ∼ 1x10 16 molec cm -2 directly over the source and increases continuously as the plume disperses. The SO 2 flux measured immediately downwind of the refinery was found to be about 1200 kg h -1 (±40% uncertainty).

Inclusion of ash and SO2 emissions from volcanic eruptions in WRF-Chem: development and some applications

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M. Stuefer

2013-04-01

Full Text Available We describe a new functionality within the Weather Research and Forecasting (WRF model with coupled Chemistry (WRF-Chem that allows simulating emission, transport, dispersion, transformation and sedimentation of pollutants released during volcanic activities. Emissions from both an explosive eruption case and a relatively calm degassing situation are considered using the most recent volcanic emission databases. A preprocessor tool provides emission fields and additional information needed to establish the initial three-dimensional cloud umbrella/vertical distribution within the transport model grid, as well as the timing and duration of an eruption. From this source condition, the transport, dispersion and sedimentation of the ash cloud can be realistically simulated by WRF-Chem using its own dynamics and physical parameterization as well as data assimilation. Examples of model applications include a comparison of tephra fall deposits from the 1989 eruption of Mount Redoubt (Alaska and the dispersion of ash from the 2010 Eyjafjallajökull eruption in Iceland. Both model applications show good coincidence between WRF-Chem and observations.

Estimating Sulfur Dioxide in Volcanic Plumes Using an Ultraviolet Camera. First Results from Lascar, Ollagüe and Irruputuncu Volcanoes

Science.gov (United States)

Geoffroy, C. A.; Amigo, A.

2014-12-01

Volcanic gas fluxes give important information on both the amount of degassing and magma reservoirs. In most of magmas, water vapor (H2O) and carbon dioxide (CO2) are major components of volcanic gas. However, sulfur dioxide (SO2) is one of the targets of remote sensing due to their low concentration in the environment and easy detection by ultraviolet spectroscopy. Accordingly, plume imaging using passive ultraviolet cameras is a relatively simple method to study volcanic degassing, expeditious manner and can be used up from distances of about 10 km from source of emissions. We estimated SO2 concentrations and fluxes in volcanic plumes with the ultraviolet camera Envicam-2, developed by Nicarnica Aviation, acquired by the Geological Survey of Chile (SERNAGEOMIN). The camera has filters that allow passage of ultraviolet radiation at wavelengths of interest. For determining whether there is absorption of radiation associated with the presence of SO2 the Beer-Lambert law was used for quantifying concentrations using appropriate calibration cells. SO2 emissions to the atmosphere were estimated using wind speed as an approximation to the plume transport. In this study we reported the implementation of a new methodology for using Envicam-2 and subsequent collection of SO2 concentrations and fluxes in passive degassing volcanoes. Measurements were done at Lascar, Ollagüe and Irruputuncu volcanoes, located in northern Chile. The volcanoes were chosen because of optimal atmospheric conditions for ultraviolet imaging. Results indicate concentrations within the expected ranges for three volcanoes generally between 400-1700 ppm•m. In the case of Láscar volcano, the emission rates of SO2 range from 250 to 500 tonnes/day for a same image of the plume. In particular, wind speed was determined from scaling images and are consistent with data from regional numerical models, as well as records of the meteorological stations installed at the ALMA astronomical center, located

Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

Science.gov (United States)

Werner, Cynthia; Kelly, Peter J.; Doukas, Michael; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert; Neal, Christina

2013-06-01

The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15-July 1, 2009) was 59 and 66% of the total CO2 and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27-0.56 wt.% S; whole-rock normalized values are slightly lower (0.8-1.7 wt.% CO2 and 0.22-0.47 wt.% S) and are similar to what was calculated for the 1989-90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional unerupted magma degassed in the

Synthesis, characterization and thermal decomposition of [Pd2 (C2-dmba (µ-SO4 (SO22

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Caires Antonio Carlos Fávero

1998-01-01

Full Text Available The bridged sulphate complex [Pd2 (C²,dmba (µ-SO4 (SO22] has been obtained by reacting a saturated solution of SO2 in methanol and the cyclometallated compound [Pd(C²,N-dmba(µ-N3] 2; (dmba = N,N-dimethylbenzylamine, at room temperature for 24 h. Reaction product was characterized by elemental analysis, NMR comprising 13C{¹H} and ¹H nuclei and I.R. spectrum's measurements. Thermal behavior has been investigated and residual products identified by X-ray powder diffraction.

Volcanic gas composition changes during the gradual decrease of the gigantic degassing activity of Miyakejima volcano, Japan, 2000-2015

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Shinohara, Hiroshi; Geshi, Nobuo; Matsushima, Nobuo; Saito, Genji; Kazahaya, Ryunosuke

2017-02-01

The composition of volcanic gases discharged from Miyakejima volcano has been monitored during the intensive degassing activity that began after the eruption in 2000. During the 15 years from 2000 to 2015, Miyakejima volcano discharged 25.5 Mt of SO2, which required degassing of 3 km3 of basaltic magma. The SO2 emission rate peaked at 50 kt/day at the end of 2000 and quickly decreased to 5 kt/day by 2003. During the early degassing period, the volcanic gas composition was constant with the CO2/SO2 = 0.8 (mol ratio), H2O/SO2 = 35, HCl/SO2 = 0.08, and SO2/H2S = 15. The SO2 emission rate decreased gradually to 0.5 kt/day by 2012, and the gas composition also changed gradually to CO2/SO2 = 1.5, H2O/SO2 = 150, HCl/SO2 = 0.15, and SO2/H2S = 6. The compositional changes are not likely caused by changes in degassing pressure or volatile heterogeneity of a magma chamber but are likely attributed to an increase of hydrothermal scrubbing caused by large decrease of the volcanic gas emission rate, suggesting a supply of gases with constant composition during the 15 years. The intensive degassing was modeled based on degassing of a convecting magma conduit. The gradual SO2 emission rate that decrease without changes in volcanic gas composition is attributed to a reduction of diameter of the convecting magma conduit.

Laboratory studies of H2SO4/H2O binary homogeneous nucleation from the SO2+OH reaction: evaluation of the experimental setup and preliminary results

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M. Kulmala

2008-08-01

Full Text Available Binary homogeneous nucleation (BHN of sulphuric acid and water (H2SO4/H2O is one of the most important atmospheric nucleation processes, but laboratory observations of this nucleation process are very limited and there are also large discrepancies between different laboratory studies. The difficulties associated with these experiments include wall loss of H2SO4 and uncertainties in estimation of H2SO4 concentration ([H2SO4] involved in nucleation. We have developed a new laboratory nucleation setup to study H2SO4/H2O BHN kinetics and provide relatively constrained [H2SO4] needed for nucleation. H2SO4 is produced from the SO2+OH→HSO3 reaction and OH radicals are produced from water vapor UV absorption. The residual [H2SO4] were measured at the end of the nucleation reactor with a chemical ionization mass spectrometer (CIMS. Wall loss factors (WLFs of H2SO4 were estimated by assuming that wall loss is diffusion limited and these calculated WLFs were in good agreement with simultaneous measurements of the initial and residual [H2SO4] with two CIMSs. The nucleation zone was estimated from numerical simulations based on the measured aerosol sizes (particle diameter, Dp and [H2SO4]. The measured BHN rates (J ranged from 0.01–220 cm−3 s−1 at the initial and residual [H2SO4] from 108−1010 cm−3, a temperature of 288 K and relative humidity (RH from 11–23%; J increased with increasing [H2SO4] and RH. J also showed a power dependence on [H2SO4] with the exponential power of 3–8. These power dependences are consistent with other laboratory studies under similar [H2SO4] and RH, but different from atmospheric field observations which showed that particle number concentrations are often linearly dependent on [H2SO4]. These results, together with a higher [H2SO4] threshold (108–109 cm−3 needed to produce the unit J measured from the laboratory studies compared to the atmospheric conditions (106–107 cm−3, imply that H2SO4/H2O BHN alone is

A Proposed Community Network For Monitoring Volcanic Emissions In Saint Lucia, Lesser Antilles

Science.gov (United States)

Joseph, E. P.; Beckles, D. M.; Robertson, R. E.; Latchman, J. L.; Edwards, S.

2013-12-01

Systematic geochemical monitoring of volcanic systems in the English-speaking islands of the Lesser Antilles was initiated by the UWI Seismic Research Centre (SRC) in 2000, as part of its volcanic surveillance programme for the English-speaking islands of the Lesser Antilles. This programme provided the first time-series observations used for the purpose of volcano monitoring in Dominica and Saint Lucia, permitted the characterization of the geothermal fluids associated with them, and established baseline studies for understanding of the hydrothermal systems during periods of quiescence (Joseph et al., 2011; Joseph et al., 2013). As part of efforts to improve and expand the capacity of SRC to provide volcanic surveillance through its geothermal monitoring programme, it is necessary to develop economically sustainable options for the monitoring of volcanic emissions/pollutants. Towards this effort we intend to work in collaboration with local authorities in Saint Lucia, to develop a monitoring network for quantifying the background exposure levels of ambient concentrations of volcanic pollutants, SO2 in air and As in waters (as health significant marker elements in the geothermal emissions) that would serve as a model for the emissions monitoring network for other volcanic islands. This programme would facilitate the building of local capacity and training to monitor the hazardous exposure, through the application and transfer of a regionally available low-cost and low-technology SO2 measurement/detection system in Saint Lucia. Existing monitoring technologies to inform evidence based health practices are too costly for small island Caribbean states, and no government policies or health services measures currently exist to address/mitigate these influences. Gases, aerosols and toxic elements from eruptive and non-eruptive volcanic activity are known to adversely affect human health and the environment (Baxter, 2000; Zhang et al., 2008). Investigations into the

Lidar sounding of volcanic plumes

Science.gov (United States)

Fiorani, Luca; Aiuppa, Alessandro; Angelini, Federico; Borelli, Rodolfo; Del Franco, Mario; Murra, Daniele; Pistilli, Marco; Puiu, Adriana; Santoro, Simone

2013-10-01

Accurate knowledge of gas composition in volcanic plumes has high scientific and societal value. On the one hand, it gives information on the geophysical processes taking place inside volcanos; on the other hand, it provides alert on possible eruptions. For this reasons, it has been suggested to monitor volcanic plumes by lidar. In particular, one of the aims of the FP7 ERC project BRIDGE is the measurement of CO2 concentration in volcanic gases by differential absorption lidar. This is a very challenging task due to the harsh environment, the narrowness and weakness of the CO2 absorption lines and the difficulty to procure a suitable laser source. This paper, after a review on remote sensing of volcanic plumes, reports on the current progress of the lidar system.

Statistical analysis of dispersal and deposition patterns of volcanic emissions from Mt. Sakurajima, Japan

Science.gov (United States)

Poulidis, Alexandros P.; Takemi, Tetsuya; Shimizu, Atsushi; Iguchi, Masato; Jenkins, Susanna F.

2018-04-01

With the eruption of Eyjafjallajökull (Iceland) in 2010, interest in the transport of volcanic ash after moderate to major eruptions has increased with regards to both the physical and the emergency hazard management aspects. However, there remain significant gaps in the understanding of the long-term behaviour of emissions from volcanoes with long periods of activity. Mt. Sakurajima (Japan) provides us with a rare opportunity to study such activity, due to its eruptive behaviour and dense observation network. In the 6-year period from 2009 to 2015, the volcano was erupting at an almost constant rate introducing approximately 500 kt of ash per month to the atmosphere. The long-term characteristics of the transport and deposition of ash and SO2 in the area surrounding the volcano are studied here using daily surface observations of suspended particulate matter (SPM) and SO2 and monthly ashfall values. Results reveal different dispersal patterns for SO2 and volcanic ash, suggesting volcanic emissions' separation in the long-term. Peak SO2 concentrations at different locations on the volcano vary up to 2 orders of magnitude and decrease steeply with distance. Airborne volcanic ash increases SPM concentrations uniformly across the area surrounding the volcano, with distance from the vent having a secondary effect. During the period studied here, the influence of volcanic emissions was identifiable both in SO2 and SPM concentrations which were, at times, over the recommended exposure limits defined by the Japanese government, European Union and the World Health Organisation. Depositional patterns of volcanic ash exhibit elements of seasonality, consistent with previous studies. Climatological and topographic effects are suspected to impact the deposition of volcanic ash away from the vent: for sampling stations located close to complex topographical elements, sharp changes in the deposition patterns were observed, with ash deposits for neighbouring stations as close as

The Cs2SO4-Ce2(SO4)3-H2SO4-H2O system at 150 and 200 deg C

International Nuclear Information System (INIS)

Bondar', S.A.; Belokoskov, V.I.; Trofimov, G.V.

1982-01-01

Solubility in the system Cs 2 SO 4 -Ce 2 (SO 4 ) 3 -H 2 SO 4 -H 2 O using the isothermal method at 150 and 200 deg C at molar ratios Cs 2 SO 4 :Ce 2 (SO 4 ) 3 =1:5 and conditions of sulfate crystallization Cs 2 SO 4 xCe 2 (SO 4 ) 3 , Ce 2 (SO 4 ) 3 x0.5H 2 SO 4 xnH 2 O (n=2-3) and Ce 2 (SO 4 ) 3 x3H 2 SO 4 are determined. Double sulfate Cs 2 SO 4 xCe 2 (SO 4 ) 3 is studied using the methods of crystallooptical, thermal, X-ray phase analyses and IR spectroscopy

Development and application of denuder sampling techniques with in situ derivatization for the determination of hydrogenbromide in volcanic plumes

Science.gov (United States)

Gutmann, Alexandra; Rüdiger, Julian; Hoffmann, Thorsten

2016-04-01

The composition of gases in volcanic plumes shifts with subsurface processes inside volcanoes. For monitoring volcanic activity by studying volcanic plumes it is essential to understand the chemical reactions inside the volcanic plume (Bobrowski and Platt, 2013). Measurements of BrO/SO2-ratio already enable insights into magmatic processes (Bobrowski and Giuffrida, 2012). Both, BrO and SO2, are measurable by Remote Sensing Techniques at a safe distance. Models suggest not a direct emission of BrO but formation due to photochemical and multiphase reactions in the gas and particle phase. These model presume HBr as first emitted species (Gerlach, 2004). So HBr is an important connecting link between easily measurable BrO/SO2-ratios and conclusions on a volcanic system. It is of high importance to know if there is a variation in the amount of HBr transformed into BrO and to gain knowledge on the factor of its dependence. Apart from depletion of surrounded ozone also decreasing or depletion of emitted HBr or even HCl could be responsible for the shift (Bobrowski and Giuffrida, 2012). Knowledge about complex processes in volcanic plumes will simplify interpretation and predictions. In this study, first applications of coated gas diffusion denuder (similar to Huang and Hoffmann, 2008) to derivatize gaseous HBr were successful. Due to the lack of adequate remote sensing techniques an in situ method was developed and will be presented in detail. The epoxide of oleic acid was determined as a suitable derivatization agent. The reaction with HBr gives 10-bromo-9-hydroxyoctadecanoic acid. Other hydrogenhalogens give corresponding products. Derivatized analytes were removed from denuder by solvent elution and subsequent analysed with gas chromatography-mass spectrometry. A limit of quantification below 1 ng was achieved. The method was applied on volcanic gas plumes at Mt. Etna in Italy in July and August 2015. The results showed HBr in higher ppt-range. These first proof

The ternary system K2SO4MgSO4CaSO4

Science.gov (United States)

Rowe, J.J.; Morey, G.W.; Silber, C.C.

1967-01-01

Melting and subsolidus relations in the system K2SO4MgSO4CaSO4 were studied using heating-cooling curves, differential thermal analysis, optics, X-ray diffraction at room and high temperatures and by quenching techniques. Previous investigators were unable to study the binary MgSO4CaSO4 system and the adjacent area in the ternary system because of the decomposition of MgSO4 and CaSO4 at high temperatures. This problem was partly overcome by a novel sealed-tube quenching method, by hydrothermal synthesis, and by long-time heating in the solidus. As a result of this study, we found: (1) a new compound, CaSO4??3MgSO4 (m.p. 1201??C) with a field extending into the ternary system; (2) a high temperature form of MgSO4 with a sluggishly reversible inversion. An X-ray diffraction pattern for this polymorphic form is given; (3) the inversion of ??-CaSO4 (anhydrite) to ??-CaSO4 at 1195??C, in agreement with grahmann; (1) (4) the melting point of MgSO4 is 1136??C and that of CaSO4 is 1462??C (using sealed tube methods to prevent decomposition of the sulphates); (5) calcium langbeinite (K2SO4??2CaSO4) is the only compound in the K2SO4CaSO4 binary system. This resolved discrepancies in the results of previous investigators; (6) a continuous solid solution series between congruently melting K2SOP4??2MgSO4 (langbeinite) and incongruently melting K2SO4??2CaSO4 (calcium langbeinite); (7) the liquidus in the ternary system consists of primary phase fields of K2SO4, MgSO4, CaSO4, langbeinite-calcium langbeinite solid solution, and CaSO4??3MgSO4. The CaSO4 field extends over a large portion of the system. Previously reported fields for the compounds (K2SO4??MgSO4??nCaSO4), K2SO4??3CaSO4 and K2SO4??CaSO4 were not found; (8) a minimum in the ternary system at: 740??C, 25% MgSO4, 6% CaSO4, 69% K2SO4; and ternary eutectics at 882??C, 49% MgSO4, 19% CaSO4, 32% K2SO4; and 880??, 67??5% MgSO4, 5% CaSO4, 27??5% K2SO4. ?? 1967.

Cs2SO4-Pr2(SO4)3-H2O and NiSO4-Pr2(SO4)3-H2O systems at 75 deg C

International Nuclear Information System (INIS)

Onishchenko, M.K.; Skorikov, V.M.; Shevchuk, V.G.; AN SSSR, Moscow. Inst. Obshchej i Neorganicheskoj Khimii)

1979-01-01

To investigate physico-chemical properties of equilibrium saturated solutions and to elucidate the chemical changes under way, the aqueous systems of cesium, nickel and praseodymium (3) sulfates are studied. The method of isothermal saturation of salts at 75 deg C is used. It has been found that in the system Cs 2 SO 4 -Pr 2 (SO 4 ) 3 -H 2 O in a wide concentration range the soluble binary salt Cs 2 SO 4 xPr 2 (SO 4 ) 3 csytallizes in a congruent way. For the system NiSO 4 -Pr 2 (SO 4 ) 3 -H 2 O a solubility curve of the eutonic type is obtained, there being no chemical interaction between the components. The solubility isotherms for the system are given

Correction of mass spectrometric isotope ratio measurements for isobaric isotopologues of O2, CO, CO2, N2O and SO2.

Science.gov (United States)

Kaiser, Jan; Röckmann, Thomas

2008-12-01

Gas isotope ratio mass spectrometers usually measure ion current ratios of molecules, not atoms. Often several isotopologues contribute to an ion current at a particular mass-to-charge ratio (m/z). Therefore, corrections have to be applied to derive the desired isotope ratios. These corrections are usually formulated in terms of isotope ratios (R), but this does not reflect the practice of measuring the ion current ratios of the sample relative to those of a reference material. Correspondingly, the relative ion current ratio differences (expressed as delta values) are first converted into isotopologue ratios, then into isotope ratios and finally back into elemental delta values. Here, we present a reformulation of this data reduction procedure entirely in terms of delta values and the 'absolute' isotope ratios of the reference material. This also shows that not the absolute isotope ratios of the reference material themselves, but only product and ratio combinations of them, are required for the data reduction. These combinations can be and, for carbon and oxygen have been, measured by conventional isotope ratio mass spectrometers. The frequently implied use of absolute isotope ratios measured by specially calibrated instruments is actually unnecessary. Following related work on CO2, we here derive data reduction equations for the species O2, CO, N2O and SO2. We also suggest experiments to measure the required absolute ratio combinations for N2O, SO2 and O2. As a prelude, we summarise historic and recent measurements of absolute isotope ratios in international isotope reference materials. Copyright 2008 John Wiley & Sons, Ltd.

Screening criteria of volcanic hazards aspect in the NPP site evaluation

International Nuclear Information System (INIS)

Nur Siwhan

2013-01-01

Studies have been conducted on the completeness of regulation in Indonesia particularly on volcanic hazards aspects in the evaluation of nuclear power plant site. Volcanic hazard aspect needed to identify potential external hazards that may endanger the safety of the operation of nuclear power plants. There are four stages for evaluating volcanic hazards, which are initial assessment, characterization sources of volcanic activity in the future, screening volcanic hazards and assessment of capable volcanic hazards. This paper discuss the third stage of the general evaluation which is the screening procedure of volcanic hazards. BAPETEN Chairman Regulation No. 2 Year of 2008 has only one screening criteria for missile volcanic phenomena, so it required screening criteria for other hazard phenomena that are pyroclastic flow density; lava flows; avalanche debris materials; lava; opening hole new eruptions, volcano missile; tsunamis; ground deformation; and hydrothermal system and ground water anomaly. (author)

Degassing of CO2, SO2, and H2S associated with the 2009 eruption of Redoubt Volcano, Alaska

Science.gov (United States)

Werner, Cynthia A.; Kelly, Peter; Doukas, Michael P.; Lopez, Taryn; Pfeffer, Melissa; McGimsey, Robert G.; Neal, Christina

2013-01-01

The 2009 eruption of Redoubt Volcano, Alaska was particularly well monitored for volcanic gas emissions. We report 35 airborne measurements of CO2, SO2, and H2S emission rates that span from October 2008 to August 2010. The magmatic system degassed primarily as a closed system although minor amounts of open system degassing were observed in the 6 months prior to eruption on March 15, 2009 and over 1 year following cessation of dome extrusion. Only 14% of the total CO2 was emitted prior to eruption even though high emissions rates (between 3630 and 9020 t/d) were observed in the final 6 weeks preceding the eruption. A minor amount of the total SO2 was observed prior to eruption (4%), which was consistent with the low emission rates at that time (up to 180 t/d). The amount of the gas emitted during the explosive and dome growth period (March 15–July 1, 2009) was 59 and 66% of the total CO2and SO2, respectively. Maximum emission rates were 33,110 t/d CO2, 16,650 t/d SO2, and 1230 t/d H2S. Post-eruptive passive degassing was responsible for 27 and 30% of the total CO2 and SO2, respectively. SO2 made up on average 92% of the total sulfur degassing throughout the eruption. Magmas were vapor saturated with a C- and S-rich volatile phase, and regardless of composition, the magmas appear to be buffered by a volatile composition with a molar CO2/SO2 ratio of ~ 2.4. Primary volatile contents calculated from degassing and erupted magma volumes range from 0.9 to 2.1 wt.% CO2 and 0.27–0.56 wt.% S; whole-rock normalized values are slightly lower (0.8–1.7 wt.% CO2 and 0.22–0.47 wt.% S) and are similar to what was calculated for the 1989–90 eruption of Redoubt. Such contents argue that primary arc magmas are rich in CO2 and S. Similar trends between volumes of estimated degassed magma and observed erupted magma during the eruptive period point to primary volatile contents of 1.25 wt.% CO2 and 0.35 wt.% S. Assuming these values, up to 30% additional

Sulfate Formation on Mars by Volcanic Aerosols: A New Look

Science.gov (United States)

Blaney, D. L.

1996-03-01

Sulfur was measured at both Viking Lander sites in abundances of 5-9 wt % SO3. Because the sulfur was more concentrated in clumps which disintegrated and the general oxidized nature of the Martian soil, these measurements led to the assumption that a sulfate duricrust existed. Two types of models for sulfate formation have been proposed. One is a formation by upwardly migrating ground water. The other is the formation of sulfates by the precipitation of volcanic aerosols. Most investigators have tended to favor the ground water origin of sulfates on Mars. However, evidence assemble since Viking may point to a volcanic aerosol origin.

Observations of the loss of stratospheric NO2 following volcanic eruptions

Science.gov (United States)

Coffey, M. T.; Mankin, William G.

1993-01-01

Observations of stratospheric column amounts of nitrogen dioxide (NO2), nitric oxide (NO) and nitric acid (HNO3) have been made following major eruptions of the El Chichon and Mt. Pintatubo volcanoes. Midlatitude abundances of NO2 and NO were reduced by as much as 70% in the months following the appearance of the volcanic aerosols as compared to volcanically quite periods. There are heterogeneous reactions which could occur on the volcanic aerosols to convert NO2 into HNO3 but no commensurate increase in HNO3 column amounts was observed at the times of NO2 decrease.

Airborne emission measurements of SO2 , NOx and particles from individual ships using a sniffer technique

Science.gov (United States)

Beecken, J.; Mellqvist, J.; Salo, K.; Ekholm, J.; Jalkanen, J.-P.

2014-07-01

A dedicated system for airborne ship emission measurements of SO2, NOx and particles has been developed and used from several small aircraft. The system has been adapted for fast response measurements at 1 Hz, and the use of several of the instruments is unique. The uncertainty of the given data is about 20% for SO2 and 24% for NOx emission factors. The mean values with one standard deviation for multiple measurements of 158 ships measured from the air on the Baltic and North Sea during 2011 and 2012 show emission factors of 18.8 ± 6.5 g kg-1 fuel , 66.6 ± 23.4 g kg-1 fuel and 1.8 ± 1.3 1016 particles kg-1 fuel for SO2, NOx and particle number, respectively. The particle size distributions were measured for particle diameters between 15 and 560 nm. The mean sizes of the particles are between 45 and 54 nm dependent on the distance to the source, and the number size distribution is monomodal. Concerning the sulfur fuel content, around 85% of the monitored ships comply with the International Maritime Organization (IMO) limits. The reduction of the sulfur emission control area (SECA) limit from 1.5 to 1% in 2010 appears to have contributed to reduction of sulfur emissions that were measured in earlier studies from 2007 to 2009. The presented method can be implemented for regular ship compliance monitoring.

Estudio del Sistema Li2SO4 – Na2SO4. Diagrama de fases y caracterización del LiNaSO4

Directory of Open Access Journals (Sweden)

Font-Bardia, M.

2004-08-01

Full Text Available An exhaustive study of the phase diagram of binary system Li2SO4-Na2SO4 is presented. Phase diagram was determined using thermo-X-ray diffraction in powder samples and calorimetry ATD. A new phase with formula Li2-xNaxSO4 has been obtained, with 1 ≤ x ≤ 1.22. The crystal structure of β-LiNaSO4 was determined from single-crystal X-ray diffraction. This study shows that the crystals usually become twinned when the growth is by solution; which explains the poor spontaneous polarization. The Raman dispersion of Li2SO4, Na2SO4 and LiNaSO4 compounds is explained from the structural data. The measurements have been made at different heating and cooling rate.Se presenta un estudio exhaustivo del diagrama de fase del sistema binario Li2SO4-Na2SO4. El diagrama de fases se determinó mediante termo-difractometría de rayos-X en muestras de polvo y calorimetría ATD. Se obtiene una nueva fase de fórmula Li2-xNaxSO4, con 1 ≤ x ≤ 1.22. La estructura cristalina de β-LiNaSO4 se determinó por difracción de rayos-X sobre un monocristal. Este estudio muestra que los cristales usualmente se maclan cuando el crecimiento es por solución, lo cual explica la baja polarización espontánea. Se explica la dispersión Raman de los compuestos Li2SO4, Na2SO4 y LiNaSO4, a partir de los datos estructurales. Las medidas experimentales se han efectuado a diferentes velocidades de calentamiento y enfriamiento.

Synergistic use of Lagrangian dispersion and radiative transfer modelling with satellite and surface remote sensing measurements for the investigation of volcanic plumes: the Mount Etna eruption of 25–27 October 2013

Directory of Open Access Journals (Sweden)

P. Sellitto

2016-06-01

Full Text Available In this paper we combine SO2 and ash plume dispersion modelling with satellite and surface remote sensing observations to study the regional influence of a relatively weak volcanic eruption from Mount Etna on the optical and micro-physical properties of Mediterranean aerosols. We analyse the Mount Etna eruption episode of 25–27 October 2013. The evolution of the plume along the trajectory is investigated by means of the FLEXible PARTicle Lagrangian dispersion (FLEXPART model. The satellite data set includes true colour images, retrieved values of volcanic SO2 and ash, estimates of SO2 and ash emission rates derived from MODIS (MODerate resolution Imaging Spectroradiometer observations and estimates of cloud top pressure from SEVIRI (Spinning Enhanced Visible and InfraRed Imager. Surface remote sensing measurements of aerosol and SO2 made at the ENEA Station for Climate Observations (35.52° N, 12.63° E; 50 m a.s.l. on the island of Lampedusa are used in the analysis. The combination of these different data sets suggests that SO2 and ash, despite the initial injection at about 7.0 km altitude, reached altitudes around 10–12 km and influenced the column average aerosol particle size distribution at a distance of more than 350 km downwind. This study indicates that even a relatively weak volcanic eruption may produce an observable effect on the aerosol properties at the regional scale. The impact of secondary sulfate particles on the aerosol size distribution at Lampedusa is discussed and estimates of the clear-sky direct aerosol radiative forcing are derived. Daily shortwave radiative forcing efficiencies, i.e. radiative forcing per unit AOD (aerosol optical depth, are calculated with the LibRadtran model. They are estimated between −39 and −48 W m−2 AOD−1 at the top of the atmosphere and between −66 and −49 W m−2 AOD−1 at the surface, with the variability in the estimates mainly depending on the

Boundary layer measurements of the OH radical in the vicinity of an isolated power plant plume - SO2 and NO2 chemical conversion times

Science.gov (United States)

Davis, D. D.; Philen, D.; Mcgee, T.; Heaps, W.

1979-01-01

Direct measurements of the OH radical in the vicinity of an isolated power plant plume are reported. These measurements were used to estimate the conversion time of SO2 to H2SO4-sulfate aerosol via the initiating step OH + SO2 + M yields HSO3. Using the near-high-noon measured value of OH (9.5 million per cu cm), resulted in a 1/e conversion time of 1.4 days. The latter lifetime would correspond to a conversion rate of about 2%/hr. When the lifetime calculation was modified to take into consideration the OH diurnal cycle, the 1/e conversion time for SO2 was found to be 4.4 days, giving an apparent overall rate of conversion of about 0.7%/hr. Similar calculations carried out for the conversion of NO2 to NHO3 resulted in 1/e lifetimes for NO2 of 2-3 h for midday time periods.

Diffuse CO2 fluxes from Santiago and Congro volcanic lakes (São Miguel, Azores archipelago)

Science.gov (United States)

Andrade, César; Cruz, José; Viveiros, Fátima; Branco, Rafael

2017-04-01

Diffuse CO2 degassing occurring in Santiago and Congro lakes, both located in depressions associated to maars from São Miguel Island (Azores, Portugal), was studied through detailed flux measurements. Four sampling campaigns were developed between 2013 and 2016 in each water body, split by the cold and wet seasons. São Miguel has an area of 744.6 km2, being the largest island of the archipelago. The geology of the island is dominated by three quiescent central volcanoes (Sete Cidades, Fogo and Furnas), linked by volcanic fissural zones (Picos and Congro Fissural Volcanic systems). The oldest volcanic systems of the island are located in its eastern part (Povoação-Nordeste). Santiago lake, with a surface area of 0.26 km2 and a depth of 30.5 m, is located inside a maar crater in the Sete Cidades volcano at an altitude of 355 m. The watershed of the lake has an area of 0.97 km2 and a surface flow estimated as 1.54x10 m3/a. A total of 1612 CO2 flux measurements using the accumulation chamber method were made at Santiago lake, 253 in the first campaign (November 2013), and 462, 475 and 422 in the three other campaigns, respectively, in April 2014, September 2016 and December 2016. The total CO2 flux estimated for this lake varies between 0.4 t d-1 and 0.59 t d-1, for the surveys performed, respectively, in November 2013 and September 2016; higher CO2 outputs of 1.57 and 5.87 t d-1 were calculated for the surveys carried out in April 2014 and December 2016. These higher CO2 emissions were associated with a period without water column stratification. Similarly to Santiago lake, Congro lake is located inside a maar, in the Congro Fissural Volcanic system, and has a surface area of 0.04 km2 with 18.5 m depth and a storage of about 2.4x105 m3/a. The lake, located at an altitude of 420 m, is fed by a watershed with an area of 0.33 km2 and a runoff estimated as about 8x104 m3/a. In Congro lake a total of 713 CO2 flux measurements were performed during four surveys from

Dissociative phototionization cross sections of H2, SO2 and H2O

International Nuclear Information System (INIS)

Chung, Y.

1989-01-01

The partial photoionization cross sections of H 2 , SO 2 , and H 2 O were calculated from the measured photoionization branching ratios and the known total photoionization cross sections. The branching ratios were measured with a time-of-flight mass spectrometer and synchrotron radiation. The branching ratios Of H 2 , SO 2 , and H 2 O were measured for 100 ∼ 410, 150 ∼ 380 and 120 ∼ 720 angstrom. The author also measured the photoionization yield Of SO 2 from 520 to 665 angstrom using a double ion chamber and a glow discharge light source. The principle of a time-of-flight mass spectrometer is explained. New calculations were made to see how the design of the mass spectrometer, applied voltage, and kinetic energy of the ions affect the overall performance of the mass spectrometer. Several useful techniques that we used at the synchrotron for wavelength calibration and higher order suppression are also discussed

Characterising volcanic cycles at Soufriere Hills Volcano, Montserrat: Time series analysis of multi-parameter satellite data

Science.gov (United States)

Flower, Verity J. B.; Carn, Simon A.

2015-10-01

The identification of cyclic volcanic activity can elucidate underlying eruption dynamics and aid volcanic hazard mitigation. Whilst satellite datasets are often analysed individually, here we exploit the multi-platform NASA A-Train satellite constellation to cross-correlate cyclical signals identified using complementary measurement techniques at Soufriere Hills Volcano (SHV), Montserrat. In this paper we present a Multi-taper (MTM) Fast Fourier Transform (FFT) analysis of coincident SO2 and thermal infrared (TIR) satellite measurements at SHV facilitating the identification of cyclical volcanic behaviour. These measurements were collected by the Ozone Monitoring Instrument (OMI) and Moderate Resolution Imaging Spectroradiometer (MODIS) (respectively) in the A-Train. We identify a correlating cycle in both the OMI and MODIS data (54-58 days), with this multi-week feature attributable to episodes of dome growth. The 50 day cycles were also identified in ground-based SO2 data at SHV, confirming the validity of our analysis and further corroborating the presence of this cycle at the volcano. In addition a 12 day cycle was identified in the OMI data, previously attributed to variable lava effusion rates on shorter timescales. OMI data also display a one week (7-8 days) cycle attributable to cyclical variations in viewing angle resulting from the orbital characteristics of the Aura satellite. Longer period cycles possibly relating to magma intrusion were identified in the OMI record (102-, 121-, and 159 days); in addition to a 238-day cycle identified in the MODIS data corresponding to periodic destabilisation of the lava dome. Through the analysis of reconstructions generated from cycles identified in the OMI and MODIS data, periods of unrest were identified, including the major dome collapse of 20th May 2006 and significant explosive event of 3rd January 2009. Our analysis confirms the potential for identification of cyclical volcanic activity through combined

Thermodynamic modeling of NH_3-CO_2-SO_2-K_2SO_4-H_2O system for combined CO_2 and SO_2 capture using aqueous NH_3

International Nuclear Information System (INIS)

Qi, Guojie; Wang, Shujuan

2017-01-01

Highlights: • A new application of aqueous NH_3 based combined CO_2 and SO_2 process was proposed. • A thermodynamic model simulated the heat of absorption and the K_2SO_4 precipitation. • The CO_2 content can be regenerated in a stripper with lower heat of desorption. • The SO_2 content can be removed by K_2SO_4 precipitation from the lean NH_3 solvent. - Abstract: A new application of aqueous NH_3 based post-combustion CO_2 and SO_2 combined capture process was proposed to simultaneously capture CO_2 and SO_2, and remove sulfite by solid (K_2SO_4) precipitation method. The thermodynamic model of the NH_3-CO_2-SO_2-K_2SO_4-H_2O system for the combined CO_2 and SO_2 capture process was developed and validated in this work to analyze the heat of CO_2 and SO_2 absorption in the NH_3-CO_2-SO_2-H_2O system, and the K_2SO_4 precipitation characteristics in the NH_3-CO_2-SO_2-K_2SO_4-H_2O system. The average heat of CO_2 absorption in the NH_3-CO_2-H_2O system at 40 °C is around −73 kJ/mol CO_2 in 2.5 wt% NH_3 with CO_2 loading between 0.2 and 0.5 C/N. The average heat of SO_2 absorption in the NH_3-SO_2-H_2O system at 40 °C is around −120 kJ/mol SO_2 in 2.5 wt% NH_3 with SO_2 loading between 0 and 0.5 S/N. The average heat of CO_2 absorption in the NH_3-CO_2-SO_2-H_2O system at 40 °C is 77, 68, and 58 kJ/mol CO_2 in 2.5 wt% NH_3 with CO_2 loading between 0.2 and 0.5 C/N, when SO_2 loading is 0, 0.1, 0.2 S/N, respectively. The solubility of K_2SO_4 increases with temperature, CO_2 and SO_2 loadings, but decreases with NH_3 concentration in the CO_2 and SO_2 loaded aqueous NH_3. The thermodynamic evaluation indicates that the combined CO_2 and SO_2 capture process could employ the typical absorption/regeneration process to simultaneously capture CO_2 and SO_2 in an absorber, thermally desorb CO_2 in a stripper, and feasibly remove sulfite (oxidized to sulfate) content by precipitating K_2SO_4 from the lean NH_3 solvent after the lean/rich heat exchanger.

Volcanic gas impacts on vegetation at Turrialba Volcano, Costa Rica

Science.gov (United States)

Teasdale, R.; Jenkins, M.; Pushnik, J.; Houpis, J. L.; Brown, D. L.

2010-12-01

Turrialba volcano is an active composite stratovolcano that is located approximately 40 km east of San Jose, Costa Rica. Seismic activity and degassing have increased since 2005, and gas compositions reflect further increased activity since 2007 peaking in January 2010 with a phreatic eruption. Gas fumes dispersed by trade winds toward the west, northwest, and southwest flanks of Turrialba volcano have caused significant vegetation kill zones, in areas important to local agriculture, including dairy pastures and potato fields, wildlife and human populations. In addition to extensive vegetative degradation is the potential for soil and water contamination and soil erosion. Summit fumarole temperatures have been measured over 200 degrees C and gas emissions are dominated by SO2; gas and vapor plumes reach up to 2 km (fumaroles and gases are measured regularly by OVSICORI-UNA). A recent network of passive air sampling, monitoring of water temperatures of hydrothermal systems, and soil pH measurements coupled with measurement of the physiological status of surrounding plants using gas exchange and fluorescence measurements to: (1) identify physiological correlations between leaf-level gas exchange and chlorophyll fluorescence measurements of plants under long term stress induced by the volcanic gas emissions, and (2) use measurements in tandem with remotely sensed reflectance-derived fluorescence ratio indices to track natural photo inhibition caused by volcanic gas emissions, for use in monitoring plant stress and photosynthetic function. Results may prove helpful in developing potential land management strategies to maintain the biological health of the area.

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

Science.gov (United States)

Kern, Christoph; Sutton, Jeff; Elias, Tamar; Lee, Robert Lopaka; Kamibayashi, Kevan P.; Antolik, Loren; Werner, Cynthia A.

2015-01-01

SO2 camera systems allow rapid two-dimensional imaging of sulfur dioxide (SO2) emitted from volcanic vents. Here, we describe the development of an SO2 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 SO2 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 SO2 camera for continuous, real-time volcano monitoring shows how this versatile technique might soon be adapted and applied to monitor SO2 degassing at other volcanoes around the world.

The Online GVP/USGS Weekly Volcanic Activity Report: Providing Timely Information About Worldwide Volcanism

Science.gov (United States)

Mayberry, G. C.; Guffanti, M. C.; Luhr, J. F.; Venzke, E. A.; Wunderman, R. L.

2001-12-01

The awesome power and intricate inner workings of volcanoes have made them a popular subject with scientists and the general public alike. About 1500 known volcanoes have been active on Earth during the Holocene, approximately 50 of which erupt per year. With so much activity occurring around the world, often in remote locations, it can be difficult to find up-to-date information about current volcanism from a reliable source. To satisfy the desire for timely volcano-related information the Smithsonian Institution and US Geological Survey combined their strengths to create the Weekly Volcanic Activity Report. The Smithsonian's Global Volcanism Program (GVP) has developed a network of correspondents while reporting worldwide volcanism for over 30 years in their monthly Bulletin of the Global Volcanism Network. The US Geological Survey's Volcano Hazards Program studies and monitors volcanoes in the United States and responds (upon invitation) to selected volcanic crises in other countries. The Weekly Volcanic Activity Report is one of the most popular sites on both organization's websites. The core of the Weekly Volcanic Activity Report is the brief summaries of current volcanic activity around the world. In addition to discussing various types of volcanism, the summaries also describe precursory activity (e.g. volcanic seismicity, deformation, and gas emissions), secondary activity (e.g. debris flows, mass wasting, and rockfalls), volcanic ash hazards to aviation, and preventative measures. The summaries are supplemented by links to definitions of technical terms found in the USGS photoglossary of volcano terms, links to information sources, and background information about reported volcanoes. The site also includes maps that highlight the location of reported volcanoes, an archive of weekly reports sorted by volcano and date, and links to commonly used acronyms. Since the Weekly Volcanic Activity Report's inception in November 2000, activity has been reported at

Infrasound and SO2 Observations of the 2011 Explosive Eruption of Nabro Volcano, Eritrea

Science.gov (United States)

Fee, D.; Carn, S. A.; Prata, F.

2011-12-01

SO2 measurements to investigate the relationship between degassing and infrasound, and to speculate on possible eruption source mechanisms. This example, in addition to other recent work, demonstrates the utility of using regional and global infrasound arrays to characterize explosive volcanic eruptions, particularly in remote and poorly monitored regions. Further, comparison of SO2 emissions and infrasound lends insight into degassing processes and shows the potential to use infrasound as a real-time, remote means to detect hazardous emissions.

Multi-source SO2 emission retrievals and consistency of satellite and surface measurements with reported emissions

NARCIS (Netherlands)

Fioletov, V.; McLinden, C.A.; Kharol, S.K.; Krotkov, N.A.; Li, C.; Joiner, J.; Moran, M.D.; Vet, R.; Visschedijk, A.J.H.; Denier Van Der Gon, H.A.C.

2017-01-01

Reported sulfur dioxide (SO2) emissions from US and Canadian sources have declined dramatically since the 1990s as a result of emission control measures. Observations from the Ozone Monitoring Instrument (OMI) on NASA's Aura satellite and ground-based in situ measurements are examined to verify

Timing and compositional evolution of Late Pleistocene to Holocene volcanism within the Harrat Rahat volcanic field, Kingdom of Saudi Arabia

Science.gov (United States)

Stelten, M. E.; Downs, D. T.; Dietterich, H. R.

2017-12-01

Harrat Rahat is one of the largest ( 20,000 km2) of 15 active Cenozoic volcanic fields that stretch 3,000 km along the western Arabian Peninsula from Yemen to Syria. The Harrat Rahat volcanic field is 310 km long (N-S) by 75 km wide (E-W), and is dominated by alkalic basalts with minor hawaiite, mugearite, benmoreite, and trachyte eruptives. The timing of volcanism within greater Harrat Rahat is poorly constrained, but field relations and geochronology indicate that northern Harrat Rahat hosted the most recent eruptions. To better constrain the timing and compositional evolution of Harrat Rahat during this recent phase, we present 743 geochemical analyses, 144 40Ar/39Ar ages, and 9 36Cl exposure ages for volcanic strata from northernmost Harrat Rahat. These data demonstrate that volcanism has been ongoing from at least 1.2 Ma to the present, with the most recent eruption known from historical accounts at 1256 CE. Basalt has erupted persistently from 1.2 Ma to the present, but more evolved volcanism has been episodic. Benmoreite erupted at 1.1 Ma and between 550 to 400 ka. Trachytic volcanism has only occurred over the past 150 ka, with the most recent eruption at 5 ka. Aside from the well-documented basaltic eruption at 1256 CE, prior workers interpreted 6 additional basaltic eruptions during the Holocene. However, our 36Cl exposure ages demonstrate that these erupted between 60 to 13 ka. Interestingly, in the northern part of our field area, where the spatial density of volcanic vents is low, young volcanism (<150 ka) is dominated by basaltic eruptions. Conversely, young volcanism in the southern part of our field area, where volcanic vent density is high, is dominated by trachyte. This observation is consistent with a process wherein the time-integrated effects of basaltic influx into the crust in the south produced a mafic intrusive complex, through which younger basaltic magmas cannot ascend. Instead, these magmas stall and produce trachyte, likely through

Robust satellite techniques for monitoring volcanic eruptions

Energy Technology Data Exchange (ETDEWEB)

Pergola, N.; Pietrapertosa, C. [Consiglio Nazionale delle Ricerche, Istituto di Metodologie Avanzate, Tito Scalo, PZ (Italy); Lacava, T.; Tramutoli, V. [Potenza Universita' della Basilicata, Potenza (Italy). Dipt. di Ingegneria e Fisica dell' Ambiente

2001-04-01

Through this paper the robust approach to monitoring volcanic aerosols by satellite is applied to an extended set of events affecting Stromboli and Etna volcanoes to assess its performance in automated detection of eruptive clouds and in monitoring pre-eruptive emission activities. Using only NOAA/AVHRR data at hand (without any specific atmospheric model or ancillary ground-based measurements) the proposed method automatically discriminates meteorological from eruptive volcanic clouds and, in several cases, identified pre-eruptive anomalies in the emission rates not identified by traditional methods. The main merit of this approach is its effectiveness in recognising field anomalies also in the presence of a highly variable surface background as well as its intrinsic exportability not only on different geographic areas but also on different satellite instrumental packages. In particular, the possibility to extend the proposed method to the incoming new MSG/SEVIRI satellite package (which is going to fly next year) with its improved spectral (specific bands for SO{sub 2}) and temporal (up to 15 min) resolutions has been evaluated representing the natural continuation of this work.

CO2-, He- and H2-broadening coefficients of SO2 for ν1 band and ground state transitions for astrophysical applications

Science.gov (United States)

Ceselin, Giorgia; Tasinato, Nicola; Puzzarini, Cristina; Pietropolli Charmet, Andrea; Stoppa, Paolo; Giorgianni, Santi

2017-12-01

The discovery of the Universe and of the interstellar medium (ISM) is based on the knowledge of the molecules that are present in those places. Most of our understanding about the composition of the ISM and planetary atmospheres has been made possible almost entirely thanks to spectroscopic observations. Sulfur dioxide, SO2, is one of the about 200 molecules that have been detected in the ISM or circumstellar shells. In addition to its astrophysical relevance, SO2 has a proved role in the Earth's atmosphere. It origins from biomass burning and volcanic eruptions and directly enters in the sulfur cycle. In this work high-resolution tunable diode laser (TDL) infrared (IR) spectroscopy and mm-/sub-mm wave spectroscopy are exploited to retrieve the broadening parameters of sulfur dioxide perturbed by H2, He and CO2. IR measurements are carried out for ν1 band transitions around 9 μm by using He and CO2 as damping gases. As far as the vibrational ground state is concerned, about 20 rotational transitions are analyzed by means of the speed dependent Voigt profile to retrieve H2- and He-broadening coefficients. From the experimental results some conclusions about the quantum number dependence of the H2-, CO2- and He-collisional cross sections are drawn. Both IR and MW experiments highlight a very weak dependence of He broadening parameters on the Ka and J rotational quantum numbers. In a similar way, also SO2-H2 broadening coefficients show a negligible dependence on the rotational quantum numbers. Conversely, when CO2 is employed as perturbing species, the observed collisional cross sections tend to decrease with increasing Ka values and to increase against J, at least over the range of quantum numbers considered. The present results provide the first systematic determination of line-by-line SO2-CO2 broadening coefficients and they are of relevance to increase the potential use of spectroscopic databases for astronomical applications.

OMS, OM(η2-SO), and OM(η2-SO)(η2-SO2) molecules (M = Ti, Zr, Hf): infrared spectra and density functional calculations.

Science.gov (United States)

Liu, Xing; Wang, Xuefeng; Wang, Qiang; Andrews, Lester

2012-07-02

Infrared spectra of the matrix isolated OMS, OM(η(2)-SO), and OM(η(2)-SO)(η(2)-SO(2)) (M = Ti, Zr, Hf) molecules were observed following laser-ablated metal atom reactions with SO(2) during condensation in solid argon and neon. The assignments for the major vibrational modes were confirmed by appropriate S(18)O(2) and (34)SO(2) isotopic shifts, and density functional vibrational frequency calculations (B3LYP and BPW91). Bonding in the initial OM(η(2)-SO) reaction products and in the OM(η(2)-SO)(η(2)-SO(2)) adduct molecules with unusual chiral structures is discussed.

Volcanism on Io

Science.gov (United States)

Davies, Ashley Gerard

2014-03-01

Preface; Introduction; Part I. Io, 1610 to 1995: Galileo to Galileo: 1. Io, 1610-1979; 2. Between Voyager and Galileo: 1979-95; 3. Galileo at Io; Part II. Planetary Volcanism: Evolution and Composition: 4. Io and Earth: formation, evolution, and interior structure; 5. Magmas and volatiles; Part III. Observing and Modeling Volcanic Activity: 6. Observations: thermal remote sensing of volcanic activity; 7. Models of effusive eruption processes; 8. Thermal evolution of volcanic eruptions; Part IV. Galileo at Io: the Volcanic Bestiary: 9. The view from Galileo; 10. The lava lake at Pele; 11. Pillan and Tvashtar: lava fountains and flows; 12. Prometheus and Amirani: Effusive activity and insulated flows; 13. Loki Patera: Io's powerhouse; 14. Other volcanoes and eruptions; Part V. Volcanism on Io: The Global View: 15. Geomorphology: paterae, shields, flows and mountains; 16. Volcanic plumes; 17. Hot spots; Part VI. Io after Galileo: 18. Volcanism on Io: a post-Galileo view; 19. The future of Io observations; Appendix 1; Appendix 2; References; Index.

Are volcanic seismic b-values high, and if so when?

Science.gov (United States)

Roberts, Nick S.; Bell, Andrew F.; Main, Ian G.

2015-12-01

The Gutenberg-Richter exponent b is a measure of the relative proportion of large and small earthquakes. It is commonly used to infer material properties such as heterogeneity, or mechanical properties such as the state of stress from earthquake populations. It is 'well known' that the b-value tends to be high or very high for volcanic earthquake populations relative to b = 1 for those of tectonic earthquakes, and that b varies significantly with time during periods of unrest. We first review the supporting evidence from 34 case studies, and identify weaknesses in this argument due predominantly to small sample size, the narrow bandwidth of magnitude scales available, variability in the methods used to assess the minimum or cutoff magnitude Mc, and to infer b. Informed by this, we use synthetic realisations to quantify the effect of choice of the cutoff magnitude on maximum likelihood estimates of b, and suggest a new work flow for this choice. We present the first quantitative estimate of the error in b introduced by uncertainties in estimating Mc, as a function of the number of events and the b-value itself. This error can significantly exceed the commonly-quoted statistical error in the estimated b-value, especially for the case that the underlying b-value is high. We apply the new methods to data sets from recent periods of unrest in El Hierro and Mount Etna. For El Hierro we confirm significantly high b-values of 1.5-2.5 prior to the 10 October 2011 eruption. For Mount Etna the b-values are indistinguishable from b = 1 within error, except during the flank eruptions at Mount Etna in 2001-2003, when 1.5 forecasting informed by b-value variability, in particular in assessing the significance of b-value variations identified by sample sizes with fewer than 200 events above the completeness threshold.

Real-time Volcanic Cloud Products and Predictions for Aviation Alerts

Science.gov (United States)

Krotkov, N. A.; Hughes, E. J.; da Silva, A. M., Jr.; Seftor, C. J.; Brentzel, K. W.; Hassinen, S.; Heinrichs, T. A.; Schneider, D. J.; Hoffman, R.; Myers, T.; Flynn, L. E.; Niu, J.; Theys, N.; Brenot, H. H.

2016-12-01

We will discuss progress of the NASA ASP project, which promotes the use of satellite volcanic SO2 (VSO2) and Ash (VA) data, and forecasting tools that enhance VA Decision Support Systems (DSS) at the VA Advisory Centers (VAACs) for prompt aviation warnings. The goals are: (1) transition NASA algorithms to NOAA for global NRT processing and integration into DSS at Washington VAAC for operational users and public dissemination; (2) Utilize Direct Broadcast capability of the Aura and SNPP satellites to process Direct Readout (DR) data at two high latitude locations in Finland and Fairbanks, Alaska to enhance VA DSS in Europe and at USGS's Alaska Volcano Observatory (AVO) and Alaska-VAAC; (3) Improve global Eulerian model-based VA/VSO2 forecasting and risk/cost assessments with Metron Aviation. Our global NRT OMI and OMPS data have been fully integrated into European Support to Aviation Control Service and NOAA operational web sites. We are transitioning OMPS processing to our partners at NOAA/NESDIS to integrate into operational processing environment. NASA's Suomi NPP Ozone Science Team, in conjunction with GSFC's Direct Readout Laboratory (DRL), have implemented Version 2 of the OMPS real-time DR processing package to generate VSO2 and VA products at the Geographic Information Network of Alaska (GINA) and the Finnish Meteorological Institute (FMI). The system provides real-time coverage over some of the most congested airspace and over many of the most active volcanoes in the world. The OMPS real time capability is now publicly available via DRL's IPOPP package. We use satellite observations to define volcanic source term estimates in the NASA GOES-5 model, which was updated allowing for the simulation of VA and VSO2 clouds. Column SO2 observations from SNPP/OMPS provide an initial estimate of the total cloud SO2 mass, and are used with backward transport analysis to make an initial cloud height estimate. Later VSO2 observations are used to "nudge" the SO2 mass

Ship-based MAX-DOAS measurements of tropospheric NO2, SO2, and HCHO distribution along the Yangtze River

Science.gov (United States)

Hong, Qianqian; Liu, Cheng; Chan, Ka Lok; Hu, Qihou; Xie, Zhouqing; Liu, Haoran; Si, Fuqi; Liu, Jianguo

2018-04-01

In this paper, we present ship-based Multi-Axis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements of tropospheric trace gases' distribution along the Yangtze River during winter 2015. The measurements were performed along the Yangtze River between Shanghai and Wuhan, covering major industrial areas in eastern China. Tropospheric vertical column densities (VCDs) of nitrogen dioxide (NO2), sulfur dioxide (SO2), and formaldehyde (HCHO) were retrieved using the air mass factor calculated by the radiative transfer model. Enhanced tropospheric NO2 and SO2 VCDs were detected over downwind areas of industrial zones over the Yangtze River. In addition, spatial distributions of atmospheric pollutants are strongly affected by meteorological conditions; i.e., positive correlations were found between concentration of pollutants and wind speed over these areas, indicating strong influence of transportation of pollutants from high-emission upwind areas along the Yangtze River. Comparison of tropospheric NO2 VCDs between ship-based MAX-DOAS and Ozone Monitoring Instrument (OMI) satellite observations shows good agreement with each other, with a Pearson correlation coefficient (R) of 0.82. In this study, the NO2 / SO2 ratio was used to estimate the relative contributions of industrial sources and vehicle emissions to ambient NO2 levels. Analysis results of the NO2 / SO2 ratio show a higher contribution of industrial NO2 emissions in Jiangsu Province, while NO2 levels in Jiangxi and Hubei provinces are mainly related to vehicle emissions. These results indicate that different pollution control strategies should be applied in different provinces. In addition, multiple linear regression analysis of ambient carbon monoxide (CO) and odd oxygen (Ox) indicated that the primary emission and secondary formation of HCHO contribute 54.4 ± 3.7 % and 39.3 ± 4.3 % to the ambient HCHO, respectively. The largest contribution from primary emissions in winter suggested that

The difficulty of measuring the absorption of scattered sunlight by H2O and CO2 in volcanic plumes: A comment on Pering et al. “A novel and inexpensive method for measuring volcanic plume water fluxes at high temporal resolution,” Remote Sens. 2017, 9, 146

Science.gov (United States)

Kern, Christoph

2017-01-01

In their recent study, Pering et al. (2017) presented a novel method for measuring volcanic water vapor fluxes. Their method is based on imaging volcanic gas and aerosol plumes using a camera sensitive to the near-infrared (NIR) absorption of water vapor. The imaging data are empirically calibrated by comparison with in situ water measurements made within the plumes. Though the presented method may give reasonable results over short time scales, the authors fail to recognize the sensitivity of the technique to light scattering on aerosols within the plume. In fact, the signals measured by Pering et al. are not related to the absorption of NIR radiation by water vapor within the plume. Instead, the measured signals are most likely caused by a change in the effective light path of the detected radiation through the atmospheric background water vapor column. Therefore, their method is actually based on establishing an empirical relationship between in-plume scattering efficiency and plume water content. Since this relationship is sensitive to plume aerosol abundance and numerous environmental factors, the method will only yield accurate results if it is calibrated very frequently using other measurement techniques.

Characteristics of volcanic gas correlated to the eruption activity; Case study in the Merapi Volcano, periods of 1990-1994

Directory of Open Access Journals (Sweden)

Priatna Priatna

2014-06-01

Full Text Available http://dx.doi.org/10.17014/ijog.vol2no4.20074Volcanic gases, collected from Gendol and Woro solfatara fields, the summit of Merapi Volcano during 1990-1994, show an increase in chemical composition of H , CO, CO , SO , and HCl prior to the volcanic events, on the contrary to the drastic decreasing water vapour. The carbon/sulfur ratio of the volcanic gases lies between 1.5 and 5.7 which means that they were derived from the fresh magma. The Apparent Equilibrium Temperature (AET which is calculated from chemical compositions of volcanic gases using reaction of SO +3H = H S+2H O showed an increasing value prior to the volcanic events. The Merapi activities lasted during August 1990 to November 1994 showed a significant increase in ratio SO /H S prior to the November 1994 pyroclastic flow. The isotopic composition of volcanic gas condensates indicates that water vapour in Gendol is directly derived from the fresh magma. On the other hand, the contamination and cooling by the subsurface water occurred around the Woro field at a shallow part. 

Observations of volcanic plumes using small balloon soundings

Science.gov (United States)

Voemel, H.

2015-12-01

Eruptions of volcanoes are very difficult to predict and for practical purposes may occur at any time. Any observing system intending to observe volcanic eruptions has to be ready at any time. Due to transport time scales, emissions of large volcanic eruptions, in particular injections into the stratosphere, may be detected at locations far from the volcano within days to weeks after the eruption. These emissions may be observed using small balloon soundings at dedicated sites. Here we present observations of particles of the Icelandic Grimsvotn eruption at the Meteorological Observatory Lindenberg, Germany in the months following the eruption and observations of opportunity of other volcanic particle events. We also present observations of the emissions of SO2 from the Turrialba volcano at San Jose, Costa Rica. We argue that dedicated sites for routine observations of the clean and perturbed atmosphere using small sounding balloons are an important element in the detection and quantification of emissions from future volcanic eruptions.

Monitoring Persistent Volcanic Emissions from Sulphur Springs, Saint Lucia: A Community Approach to Disaster Risk Reduction

Science.gov (United States)

Joseph, E. P.; Beckles, D. M.; Cox, L.; Jackson, V. B.; Alexander, D.

2014-12-01

Volcanic and geothermal emissions are known natural sources of volatiles to the atmosphere. Volcanogenic air pollutants known to cause the most serious impact are carbon dioxide (CO2), sulphur dioxide (SO2), hydrogen chloride (HCl) and hydrogen fluoride (HF). Some studies into the potential for volcanic emissions to produce chronic diseases in humans indicate that areas of major concern include respiratory problems, particularly silicosis (Allen et al. 2000; Baxter et al. 1999; Buist et al. 1986), psychological stress (Shore et al. 1986), and chemical impacts of gas or ash (Giammanco et al. 1998). Sulphur Springs Park in Saint Lucia has a very high recreational value with >200,000 visitors annually, while the nearby town of Soufrière has >8,400 residents. Residents and visitors have raised concerns about the volcanic emissions and its health effects. As part of the volcanic surveillance programme undertaken by the UWI, Seismic Research Centre (SRC) in Saint Lucia, a new monitoring network has been established for quantifying the ambient SO2 in air, to which staff and visitors at the volcanic park are exposed to. The implementation and continued operation of this network has involved the training of local personnel in the active field sampling and analytical techniques required for the assessment of ambient SO2 concentrations, using a low cost monitor as well as commercial passive samplers. This approach recognizes that environmental hazards are a usual part of life and productive livelihoods, and to minimize post-disaster response and recovery it is beneficial to promote preparedness and mitigation, which is best achieved at the local level with community involvement. It is also intended that the volcanic emissions monitoring network could be used as a method to establish and maintain community-based initiatives that would also be helpful when volcanic threat manifests.

Indirect Climatic Effects of Major Volcanic Eruptions

Science.gov (United States)

Hofmann, D. J.

2007-05-01

The direct effects on climate, related to atmospheric emissions to the atmosphere following major volcanic eruptions, are well-known although the sparseness of such eruptions make detailed study on the range of such variations difficult. In general terms, infrared absorption by volcanic emissions to the stratosphere result in local heating early in the event when gaseous sulfur compounds exist. This early period is followed by gas to particle conversion, on a time scale of 1-2 months, promoting the formation of sulfuric acid-water droplets. Coagulation and droplet growth result in the "volcanic stratospheric aerosol layer" which is related to the predominant direct climatic effect of large eruptions, the cooling of the troposphere by backscattering of solar visible radiation to space with a recovery time scale of 1-2 years. In this paper we will discuss some of the less-known "indirect" effects of the volcanic stratospheric aerosol on climate. We label them indirect as they act on climate through intermediary atmospheric constituents. The intermediaries in the volcanic indirect climatic effect are generally atmospheric greenhouse gases or other atmospheric gases and conditions which affect greenhouse gases. For example, cooling of the troposphere following major eruptions reduces the growth rate of atmospheric carbon dioxide related to respiration by the terrestrial biosphere. In addition, redirection of part of the direct solar beam into diffuse radiation by the volcanic stratospheric aerosol stimulates plant photosynthesis, further reducing the carbon dioxide growth rate. The growth rate of the second-most important atmospheric greenhouse gas, methane, is also affected by volcanic emissions. Volcanic stratospheric aerosol particles provide surface area which catalyzes heterogeneous chemical reactions thus stimulating removal of stratospheric ozone, also a greenhouse gas. Although major droughts usually related to ENSO events have opposite effects on carbon

Dry deposition of O_3 and SO_2 estimated from gradient measurements above a temperate mixed forest

International Nuclear Information System (INIS)

Wu, Zhiyong; Staebler, Ralf; Vet, Robert; Zhang, Leiming

2016-01-01

Vertical profiles of O_3 and SO_2 concentrations were monitored at the Borden Forest site in southern Ontario, Canada from May 2008 to April 2013. A modified gradient method (MGM) was applied to estimate O_3 and SO_2 dry deposition fluxes using concentration gradients between a level above and a level below the canopy top. The calculated five-year mean (median) dry deposition velocity (V_d) were 0.35 (0.27) and 0.59 (0.54) cm s"−"1, respectively, for O_3 and SO_2. V_d(O_3) exhibited large seasonal variations with the highest monthly mean of 0.68 cm s"−"1 in August and the lowest of 0.09 cm s"−"1 in February. In contrast, seasonal variations of V_d(SO_2) were smaller with monthly means ranging from 0.48 (May) to 0.81 cm s"−"1 (December). The different seasonal variations between O_3 and SO_2 were caused by the enhanced SO_2 uptake by snow surfaces in winter. Diurnal variations showed a peak value of V_d in early morning in summer months for both O_3 and SO_2. Canopy wetness increased the non-stomatal uptake of O_3 while decreasing the stomatal uptake. This also applied to SO_2, but additional factors such as surface acidity also played an important role on the overall uptake. - Highlights: • Application of a modified gradient-method for quantifying dry deposition is demonstrated. • A five-year dry deposition database is developed for O_3 and SO_2 over a mixed forest. • Canopy wetness enhances non-stomatal O_3 uptake while inhibits stomatal uptake. • High surface acidity reduces SO_2 dry deposition. - Capsule: A five-year dataset of O_3 and SO_2 dry deposition velocities was generated from concentration gradient measurement data using a modified gradient method.

Gaseous (DMS, MSA, SO2, H2SO4 and DMSO and particulate (sulfate and methanesulfonate sulfur species over the northeastern coast of Crete

Directory of Open Access Journals (Sweden)

H. Bardouki

2003-01-01

Full Text Available A detailed study of the levels, the temporal and diurnal variability of the main compounds involved in the biogenic sulfur cycle was carried out in Crete (Eastern Mediterranean during the Mediterranean Intensive Oxidant Study (MINOS field experiment in July-August 2001. Intensive measurements of gaseous dimethylsulfide (DMS, dimethylsulfoxide (DMSO, sulfur dioxide (SO2, sulfuric (H2SO4 and methanesulfonic acids (MSA and particulate sulfate (SO42- and methanesulfonate (MS- have been performed during the campaign. Dimethylsulfide (DMS levels ranged from 2.9 to 136 pmol·mol-1 (mean value of 21.7 pmol·mol-1 and showed a clear diurnal variation with daytime maximum. During nighttime DMS levels fall close or below the detection limit of 2 pmol·mol-1. Concurrent measurements of OH and NO3 radicals during the campaign indicate that NO3 levels can explain most of the observed diurnal variation of DMS. Dimethylsulfoxide (DMSO ranged between 0.02 and 10.1 pmol·mol-1 (mean value of 1.7 pmol·mol-1 and presents a diurnal variation similar to that of DMS. SO2 levels ranged from 220 to 2970 pmol·mol-1 (mean value of 1030 pmol·mol-1, while nss-SO42- and MS- ranged from 330 to 7100 pmol·mol-1, (mean value of 1440 pmol·mol-1 and 1.1 to 37.5 pmol·mol-1 (mean value of 11.5 pmol·mol-1 respectively. Of particular interest are the measurements of gaseous MSA and H2SO4. MSA ranged from below the detection limit (3x104 to 3.7x107 molecules cm-3, whereas H2SO4 ranged between 1x105 and 9.0x107 molecules cm-3. The measured H2SO4 maxima are among the highest reported in literature and can be attributed to high insolation, absence of precipitation and increased SO2 levels in the area. From the concurrent SO2, OH, and H2SO4 measurements a sticking coefficient of 0.52±0.28 was calculated for H2SO4. From the concurrent MSA, OH, and DMS measurements the yield of gaseous MSA from the OH-initiated oxidation of DMS was calculated to range between 0.1-0.4%. This low MSA

Volcanic eruption plumes on Io

International Nuclear Information System (INIS)

Strom, R.G.; Terrile, R.J.; Masursky, H.; Hansen, C.

1979-01-01

The detection of an umbrella-shaped plume extending about 280 km above the bright limb of Io was one of the most important discoveries made during the Voyager 1 encounter with the jovian system. This discovery proves that Io is volcanically active at present, and the number and magnitude of these eruptions indicate that Io is the most volcanically active body so far discovered in the Solar System. Preliminary analyses of these eruptive plumes are presented. (U.K.)

Lessons Learned from OMI Observations of Point Source SO2 Pollution

Science.gov (United States)

Krotkov, N.; Fioletov, V.; McLinden, Chris

2011-01-01

The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. Although anthropogenic SO2 signals may not be detectable in a single OMI pixel, it is possible to see the source and determine its exact location by averaging a large number of individual measurements. We describe new techniques for spatial and temporal averaging that have been applied to the OMI SO2 data to determine the spatial distributions or "fingerprints" of SO2 burdens from top 100 pollution sources in North America. The technique requires averaging of several years of OMI daily measurements to observe SO2 pollution from typical anthropogenic sources. We found that the largest point sources of SO2 in the U.S. produce elevated SO2 values over a relatively small area - within 20-30 km radius. Therefore, one needs higher than OMI spatial resolution to monitor typical SO2 sources. TROPOMI instrument on the ESA Sentinel 5 precursor mission will have improved ground resolution (approximately 7 km at nadir), but is limited to once a day measurement. A pointable geostationary UVB spectrometer with variable spatial resolution and flexible sampling frequency could potentially achieve the goal of daily monitoring of SO2 point sources and resolve downwind plumes. This concept of taking the measurements at high frequency to enhance weak signals needs to be demonstrated with a GEOCAPE precursor mission before 2020, which will help formulating GEOCAPE measurement requirements.

Fumarole/plume and diffuse CO2 emission from Sierra Negra volcano, Galapagos archipelago

Science.gov (United States)

Padron, E.; Hernandez Perez, P. A.; Perez, N.; Theofilos, T.; Melian, G.; Barrancos, J.; Virgil, G.; Sumino, H.; Notsu, K.

2009-12-01

The active shield-volcano Sierra Negra is part of the Galapagos hotspot. Sierra Negra is the largest shield volcano of Isabela Island, hosting a 10 km diameter caldera. Ten historic eruptions have occurred and some involved a frequently visited east caldera rim fissure zone called Volcan Chico. The last volcanic event occurred in October 2005 and lasted for about a week, covering approximately twenty percent of the eastern caldera floor. Sierra Negra volcano has experienced some significant changes in the chemical composition of its volcanic gas discharges after the 2005 eruption. This volcanic event produced an important SO2 degassing that depleted the magmatic content of this gas. Not significant changes in the MORB and plume-type helium contribution were observed after the 2005 eruption, with a 65.5 % of MORB and 35.5 % of plume contribution. In 2006 a visible and diffuse gas emission study was performed at the summit of Sierra Negra volcano, Galapagos, to evaluate degassing rate from this volcanic system. Diffuse degassing at Sierra Negra was mainly confined in three different DDS: Volcan Chico, the southern inner margin of the caldera, and Mina Azufral. These areas showed also visible degassing, which indicates highly fractured areas where volcano-hydrothermal fluids migrate towards surface. A total fumarole/plume SO2 emission of 11 ± 2 td-1 was calculated by mini-DOAS ground-based measurements at Mina Azufral fumarolic area. Molar ratios of major volcanic gas components were also measured in-situ at Mina Azufral with a portable multisensor. The results showed H2S/SO2, CO2/SO2 and H2O/SO2 molar ratios of 0.41, 52.2 and 867.9, respectively. Multiplying the observed SO2 emission rate times the observed (gas)i/SO2 mass ratio we have estimated other volatiles emission rates. The results showed that H2O, CO2 and H2S emission rates from Sierra Negra are 562, 394, and 2.4 t d-1, respectively. The estimated total output of diffuse CO2 emission from the summit of

Detection of transient infrared absorption of SO3 and 1,3,2-dioxathietane-2,2-dioxide [cyc-(CH2)O(SO2)O] in the reaction CH2OO+SO2

Science.gov (United States)

Wang, Yi-Ying; Dash, Manas Ranjan; Chung, Chao-Yu; Lee, Yuan-Pern

2018-02-01

We recorded time-resolved infrared absorption spectra of transient species produced on irradiation at 308 nm of a flowing mixture of CH2I2/O2/N2/SO2 at 298 K. Bands of CH2OO were observed initially upon irradiation; their decrease in intensity was accompanied by the appearance of an intense band at 1391.5 cm-1 that is associated with the degenerate SO-stretching mode of SO3, two major bands of HCHO at 1502 and 1745 cm-1, and five new bands near >1340, 1225, 1100, 940, and 880 cm-1. The band near 1340 cm-1 was interfered by absorption of SO2 and SO3, so its band maximum might be greater than 1340 cm-1. SO3 in its internally excited states was produced initially and became thermalized at a later period. The rotational contour of the band of thermalized SO3 agrees satisfactorily with the reported spectrum of SO3. These five new bands are tentatively assigned to an intermediate 1,3,2-dioxathietane-2,2-dioxide [cyc-(CH2)O(SO2)O] according to comparison with anharmonic vibrational wavenumbers and relative IR intensities predicted for this intermediate. Observation of a small amount of cyc-(CH2)O(SO2)O is consistent with the expected reaction according to the potential energy scheme predicted previously. SO3+HCHO are the major products of the title reaction. The other predicted product channel HCOOH+SO2 was unobserved and its branching ratio was estimated to be <5%.

Methanesulfonates of high-valent metals. Syntheses and structural features of MoO_2(CH_3SO_3)_2, UO_2(CH_3SO_3)_2, ReO_3(CH_3SO_3), VO(CH_3SO_3)_2, and V_2O_3(CH_3SO_3)_4 and their thermal decomposition under N_2 and O_2 atmosphere

International Nuclear Information System (INIS)

Betke, Ulf; Neuschulz, Kai; Wickleder, Mathias S.

2011-01-01

Oxide methanesulfonates of Mo, U, Re, and V have been prepared by reaction of MoO_3, UO_2(CH_3COO)_2.2 H_2O, Re_2O_7(H_2O)_2, and V_2O_5 with CH_3SO_3H or mixtures thereof with its anhydride. These compounds are the first examples of solvent-free oxide methanesulfonates of these elements. MoO_2(CH_3SO_3)_2 (Pbca, a=1487.05(4), b=752.55(2), c=1549.61(5) pm, V=1.73414(9) nm"3, Z=8) contains [MoO_2] moieties connected by [CH_3SO_3] ions to form layers parallel to (100). UO_2(CH_3SO_3)_2 (P2_1/c, a=1320.4(1), b=1014.41(6), c=1533.7(1) pm, β=112.80(1) "c"i"r"c"l"e, V=1.8937(3) nm"3, Z=8) consists of linear UO_2"2"+ ions coordinated by five [CH_3SO_3] ions, forming a layer structure. VO(CH_3SO_3)_2 (P2_1/c, a=1136.5(1), b=869.87(7), c=915.5(1) pm, β=113.66(1) "c"i"r"c"l"e, V=0.8290(2) nm"3, Z=4) contains [VO] units connected by methanesulfonate anions to form corrugated layers parallel to (100). In ReO_3(CH_3SO_3) (P anti 1, a=574.0(1), b=1279.6(3), c=1641.9(3) pm, α=102.08(2), β=96.11(2), γ=99.04(2) "c"i"r"c"l"e, V=1.1523(4) nm"3, Z=8) a chain structure exhibiting infinite O-[ReO_2]-O-[ReO_2]-O chains is formed. Each [ReO_2]-O-[ReO_2] unit is coordinated by two bidentate [CH_3SO_3] ions. V_2O_3(CH_3SO_3)_4 (I2/a, a=1645.2(3), b=583.1(1), c=1670.2(3) pm, β=102.58(3), V=1.5637(5) pm"3, Z=4) adopts a chain structure, too, but contains discrete [VO]-O-[VO] moieties, each coordinated by two bidentate [CH_3SO_3] ligands. Additional methanesulfonate ions connect the [V_2O_3] groups along [001]. Thermal decomposition of the compounds was monitored under N_2 and O_2 atmosphere by thermogravimetric/differential thermal analysis and XRD measurements. Under N_2 the decomposition proceeds with reduction of the metal leading to the oxides MoO_2, U_3O_7, V_4O_7, and VO_2; for MoO_2(CH_3SO_3)_2, a small amount of MoS_2 is formed. If the thermal decomposition is carried out in a atmosphere of O_2 the oxides MoO_3 and V_2O_5 are formed. (Copyright copyright 2011 WILEY-VCH Verlag

Time-related variation of volatile contents of Western Ghats volcanic formations, Deccan, India

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Marzoli, Andrea; Callegaro, Sara; Baker, Don R.; De Min, Angelo; Renne, Paul R.

2016-04-01

Deccan volcanism in India covered more than 1 million square km and reached a maximum thickness of about 3 km, as presently preserved in the Western Ghats volcanic lava piles. Volcanic activity started at about 66.4 Ma (Jawhar formation) and ended at about 65.5 Ma (Mahabaleshwar unit; Renne et al., 2015). Deccan volcanism straddled the Cretaceous-Paleogene boundary (ca. 66.0 Ma) and possibly contributed to the end-Cretaceous mass extinction event through emission of gases such as SO2, CO2, Cl, F that may have triggered global climate changes. Severe pollution by volcanic gases is supported by the high S and Cl contents (up to 1400 and up to 900 ppm, respectively; Self et al., 2008) measured in a few olivine- and plagioclase-hosted melt inclusions from the Jawhar, Neral, and Thakurvadi Formations (early lava flows, ca. 66.3-66.4 ± 0.1 Ma; Renne et al., 2015) and by magmatic S contents (up to 1800 ppm; Callegaro et al., 2014) calculated from S measurements in clinopyroxenes from the Mahabaleshwar unit (ca. 65.5 ± 0.1; Schoene et al., 2015). Here, we present new analyses of S, Cl, and F, obtained by ion-probe and synchrotron light micro-fluorescence analyses on clinopyroxenes and plagioclase phenocrysts from ?al? lava flow units of the Western Ghats. The volatile contents of the host magmas have been calculated from recently published clinopyroxene/basalt partition coefficients. These new data will describe the time-related variation of volatile elements hosted and eventually emitted by Deccan lavas and shed light on their environmental impact. References: Callegaro S. et al. (2014). Geology 42, 895-898. Renne P.R. et al. (2015). Science 350, 76-78. Schoene B. et al. (2015). Science 347, 192-184. Self S. et al. (2008). Science 319, 1654-1657.

Long-term autonomous volcanic gas monitoring with Multi-GAS at Mount St. Helens, Washington, and Augustine Volcano, Alaska

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Kelly, P. J.; Ketner, D. M.; Kern, C.; Lahusen, R. G.; Lockett, C.; Parker, T.; Paskievitch, J.; Pauk, B.; Rinehart, A.; Werner, C. A.

2015-12-01

In recent years, the USGS Volcano Hazards Program has worked to implement continuous real-time in situ volcanic gas monitoring at volcanoes in the Cascade Range and Alaska. The main goal of this ongoing effort is to better link the compositions of volcanic gases to other real-time monitoring data, such as seismicity and deformation, in order to improve baseline monitoring and early detection of volcanic unrest. Due to the remote and difficult-to-access nature of volcanic-gas monitoring sites in the Cascades and Alaska, we developed Multi-GAS instruments that can operate unattended for long periods of time with minimal direct maintenance from field personnel. Our Multi-GAS stations measure H2O, CO2, SO2, and H2S gas concentrations, are comprised entirely of commercial off-the-shelf components, and are powered by small solar energy systems. One notable feature of our Multi-GAS stations is that they include a unique capability to perform automated CO2, SO2, and H2S sensor verifications using portable gas standards while deployed in the field, thereby allowing for rigorous tracking of sensor performances. In addition, we have developed novel onboard data-processing routines that allow diagnostic and monitoring data - including gas ratios (e.g. CO2/SO2) - to be streamed in real time to internal observatory and public web pages without user input. Here we present over one year of continuous data from a permanent Multi-GAS station installed in August 2014 in the crater of Mount St. Helens, Washington, and several months of data from a station installed near the summit of Augustine Volcano, Alaska in June 2015. Data from the Mount St. Helens Multi-GAS station has been streaming to a public USGS site since early 2015, a first for a permanent Multi-GAS site. Neither station has detected significant changes in gas concentrations or compositions since they were installed, consistent with low levels of seismicity and deformation.

SO2 emission scenarios of eastern China

International Nuclear Information System (INIS)

Qi, L.; Hao, J.; Lu, M.

1995-01-01

Under the National Key Project in Eighth Five-year Plan, a study was carried out on forecasting SO 2 emission from coal combustion in China, with a special emphasis on the eastern area. 3 scenarios, i.e. 'Optimistic', 'Pessimistic' and 'Business as Usual' scenarios were developed trying to cover changing scale of coal consumption and SO 2 emission from 1990 to 2020. A 'Top-down' approach was employed, and coal consumption elasticity was defined to project future economic growth and coal consumption. SO 2 emission scenarios were outlined, based on coal consumption, estimated sulfur content level and prospective SO 2 control situation. Emission level for each 1 degree longitude x 1 degree latitude grid cell within eastern China was also estimated to show geographical distribution of SO 2 sources. The results show that SO 2 emission in China will increase rapidly, if the current situation for energy saving and SO 2 control is maintained without improvement; measures enhanced reasonably with economic growth could stop further increase of emission by 2010. Realization of more encouraging objective to keep emission at even below 1990 level needs, however, more stringent options. The share of eastern China in the country's total emission would increase until 2000, while the general changing tendency would principally follow the scenarios of the whole country. 4 refs., 5 figs., 1 tab

Release of Volatiles During North Atlantic Flood Basalt Volcanism and Correlation to the Paleocene-Eocene Thermal Maximum

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Pedersen, J. M.; Tegner, C.; Kent, A. J.; Ulrich, T.

2017-12-01

The opening of the North Atlantic Ocean between Greenland and Norway during the lower Tertiary led to intense flood basalt volcanism and the emplacement of the North Atlantic Igneous Province (NAIP). The volcanism is temporally overlapping with the Paleocene-Eocene Thermal Maximum (PETM), but ash stratigraphy and geochronology suggests that the main flood basalt sequence in East Greenland postdates the PETM. Significant environmental changes during the PETM have been attributed to the release of CO2 or methane gas due to either extensive melting of hydrates at the ocean floor or as a consequence of the interaction of mantle derived magmas with carbon rich sediments.Estimates suggest that a minimum of 1.8x106 km3 of basaltic lava erupted during North Atlantic flood basalt volcanism. Based on measurements of melt inclusions from the flood basalts our preliminary calculations suggest that approximately 2300 Gt of SO2 and 600 Gt of HCl were released into the atmosphere. Calculated yearly fluxes approach 23 Mt/y SO2 and 6 Mt/y HCl. These estimates are regarded as conservative.The S released into to the atmosphere during flood basalt volcanism can form acid aerosols that absorb and reflect solar radiation, causing an effective cooling effect. The climatic effects of the release of Cl into the atmosphere are not well constrained, but may be an important factor for extinction scenarios due to destruction of the ozone layer.The climatic changes due to the release of S and Cl in these amounts, and for periods extending for hundred thousand of years, although not yet fully constrained are likely to be significant. One consequence of the North Atlantic flood basalt volcanism may have been the initiation of global cooling to end the PETM.

Improved optical flow velocity analysis in SO2 camera images of volcanic plumes - implications for emission-rate retrievals investigated at Mt Etna, Italy and Guallatiri, Chile

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Gliß, Jonas; Stebel, Kerstin; Kylling, Arve; Sudbø, Aasmund

2018-02-01

Accurate gas velocity measurements in emission plumes are highly desirable for various atmospheric remote sensing applications. The imaging technique of UV SO2 cameras is commonly used to monitor SO2 emissions from volcanoes and anthropogenic sources (e.g. power plants, ships). The camera systems capture the emission plumes at high spatial and temporal resolution. This allows the gas velocities in the plume to be retrieved directly from the images. The latter can be measured at a pixel level using optical flow (OF) algorithms. This is particularly advantageous under turbulent plume conditions. However, OF algorithms intrinsically rely on contrast in the images and often fail to detect motion in low-contrast image areas. We present a new method to identify ill-constrained OF motion vectors and replace them using the local average velocity vector. The latter is derived based on histograms of the retrieved OF motion fields. The new method is applied to two example data sets recorded at Mt Etna (Italy) and Guallatiri (Chile). We show that in many cases, the uncorrected OF yields significantly underestimated SO2 emission rates. We further show that our proposed correction can account for this and that it significantly improves the reliability of optical-flow-based gas velocity retrievals. In the case of Mt Etna, the SO2 emissions of the north-eastern crater are investigated. The corrected SO2 emission rates range between 4.8 and 10.7 kg s-1 (average of 7.1 ± 1.3 kg s-1) and are in good agreement with previously reported values. For the Guallatiri data, the emissions of the central crater and a fumarolic field are investigated. The retrieved SO2 emission rates are between 0.5 and 2.9 kg s-1 (average of 1.3 ± 0.5 kg s-1) and provide the first report of SO2 emissions from this remotely located and inaccessible volcano.

The Detection, Characterization and Tracking of Recent Aleutian Island Volcanic Ash Plumes and the Assessment of Their Impact on Aviation

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Murray, John J.; Hudnall, L. A.; Matus, A.; Krueger, A. J.; Trepte, C. r.

2010-01-01

The Aleutian Islands of Alaska are home to a number of major volcanoes which periodically present a significant hazard to aviation. During summer of 2008, the Okmok and Kasatochi volcanoes experienced moderate eruptive events. These were followed a dramatic, major eruption of Mount Redoubt in late March 2009. The Redoubt case is extensively covered in this paper. Volcanic ash and SO2 from each of these eruptions dispersed throughout the atmosphere. This created the potential for major problems for air traffic near the ash dispersions and at significant distances downwind. The NASA Applied Sciences Weather Program implements a wide variety of research projects to develop volcanic ash detection, characterization and tracking applications for NASA Earth Observing System and NOAA GOES and POES satellites. Chemistry applications using NASA AURA satellite Ozone Monitoring System (OMI) retrievals produced SO2 measurements to trace the dispersion of volcanic aerosol. This work was complimented by advanced multi-channel imager applications for the discrimination and height assignment of volcanic ash using NASA MODIS and NOAA GOES and POES imager data. Instruments similar to MODIS and OMI are scheduled for operational deployment on NPOESS. In addition, the NASA Calipso satellite provided highly accurate measurements of aerosol height and dispersion for the calibration and validation of these algorithms and for corroborative research studies. All of this work shortens the lead time for transition to operations and ensures that research satellite data and applications are operationally relevant and utilized quickly after the deployment of operational satellite systems. Introduction

Remote measurement of high preeruptive water vapor emissions at Sabancaya volcano by passive differential optical absorption spectroscopy

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Kern, Christoph; Masias, Pablo; Apaza, Fredy; Reath, Kevin; Platt, Ulrich

2017-01-01

Water (H2O) is by far the most abundant volcanic volatile species and plays a predominant role in driving volcanic eruptions. However, numerous difficulties associated with making accurate measurements of water vapor in volcanic plumes have limited their use as a diagnostic tool. Here we present the first detection of water vapor in a volcanic plume using passive visible-light differential optical absorption spectroscopy (DOAS). Ultraviolet and visible-light DOAS measurements were made on 21 May 2016 at Sabancaya Volcano, Peru. We find that Sabancaya's plume contained an exceptionally high relative water vapor abundance 6 months prior to its November 2016 eruption. Our measurements yielded average sulfur dioxide (SO2) emission rates of 800–900 t/d, H2O emission rates of around 250,000 t/d, and an H2O/SO2 molecular ratio of 1000 which is about an order of magnitude larger than typically found in high-temperature volcanic gases. We attribute the high water vapor emissions to a boiling-off of Sabancaya's hydrothermal system caused by intrusion of magma to shallow depths. This hypothesis is supported by a significant increase in the thermal output of the volcanic edifice detected in infrared satellite imagery leading up to and after our measurements. Though the measurement conditions encountered at Sabancaya were very favorable for our experiment, we show that visible-light DOAS systems could be used to measure water vapor emissions at numerous other high-elevation volcanoes. Such measurements would provide observatories with additional information particularly useful for forecasting eruptions at volcanoes harboring significant hydrothermal systems.

Improvement of the tetrachloromercurate absorption technique for measuring low atmospheric SO2 mixing ratios

Science.gov (United States)

Jaeschke, W.; Beltz, N.; Haunold, W.; Krischke, U.

1997-07-01

During the Gas-Phase Sulfur Intercomparison Experiment (GASIE) in 1994 an analytical system for measuring sulfur dioxide mixing ratios at low parts per trillion (pptv) levels was employed. It is based on the absorption of SO2 on a tetrachloromercurate(II)-impregnated filter. The subsequent analysis uses a chemiluminescence reaction by treating the resulting disulfitomercurate(II) complex with an acidic cerium sulfate solution. An improved sampling device has been introduced that increases the maximum sampling volume from 200 L to 500 L. It is also possible to determine the blank value accurately for each sample. The absorption efficiency of the sampling system is 98.7±6.4% at a nominal flow rate of 10 L/min. The calculated (3σ) detection limit is 3±1 pptv SO2. The sample solution is stable for up to 30 days, which allows the samples to be safely stored or shipped before analysis. This permits the use of a sensitive, compact, and reliable sampling system in the field with subsequent analysis under optimal conditions in the laboratory. A continuous flow chemiluminescence (CFCL) analyzer for on-line measurements is also presented. The system is based on the same chemical principles as the described filter technique.

Physical and optical properties of 2010 Eyjafjallajökull volcanic eruption aerosol: ground-based, Lidar and airborne measurements in France

Directory of Open Access Journals (Sweden)

M. Hervo

2012-02-01

Full Text Available During the Eyjafjallajökull eruption (14 April to 24 May 2010, the volcanic aerosol cloud was observed across Europe by several airborne in situ and ground-based remote-sensing instruments. On 18 and 19 May, layers of depolarizing particles (i.e. non-spherical particles were detected in the free troposphere above the Puy de Dôme station, (PdD, France with a Rayleigh-Mie LIDAR emitting at a wavelength of 355 nm, with parallel and crossed polarization channels. These layers in the free troposphere (FT were also well captured by simulations with the Lagrangian particle dispersion model FLEXPART, which furthermore showed that the ash was eventually entrained into the planetary boundary layer (PBL. Indeed, the ash cloud was then detected and characterized with a comprehensive set of in situ instruments at the Puy de Dôme station (PdD. In agreement with the FLEXPART simulation, up to 65 μg m⁻³ of particle mass and 2.2 ppb of SO₂ were measured at PdD, corresponding to concentrations higher than the 95 percentile of 2 yr of measurements at PdD. Moreover, the number concentration of particles increased to 24 000 cm⁻³, mainly in the submicronic mode, but a supermicronic mode was also detected with a modal diameter of 2 μm. The resulting optical properties of the ash aerosol were characterized by a low scattering Ångström exponent (0.98, showing the presence of supermicronic particles. For the first time to our knowledge, the combination of in situ optical and physical characterization of the volcanic ash allowed the calculation of the mass-to-extinction ratio (η with no assumptions on the aerosol density. The mass-to-extinction ratio was found to be significantly different from the background boundary layer aerosol (max: 1.57 g m⁻² as opposed to 0.33 ± 0.03 g m⁻². Using this ratio, ash mass concentration in the volcanic plume derived from LIDAR measurements was found to be 655 ± 23 �

Measurement of thermal neutron fluence with CaSO4 thermoluminescent phosphors

International Nuclear Information System (INIS)

Liu Jinhua; Su Jingling; Wei Zemin

1984-01-01

During neutron irradiation, some TL phosphors were activated. After leaving the irradiation field the TL phosphor produced self-irradiation. The TL output of self-dose was only related to the original neutron fluence and independent of the γ-radiation. Several CaSO 4 TL phosphors were made. They were CaSO 4 :Dy, CaSO 4 :Dy-Teflon, CaSO 4 :Dy mixed with Dy 2 O 3 , CaSO 4 :Mn mixed with Dy 2 O 3 . The linearity, and lower detection limits of these TL phosphors were measured. The thermal neutron response of CaSO 4 :Mn mixed with Dy 2 O 3 was 64 R/(10 10 cm -2 ) and the lower detection limit was 1.3x10 5 cm -2

Study on in-situ electrochemical impedance spectroscopy measurement of anodic reaction in SO_2 depolarized electrolysis process

International Nuclear Information System (INIS)

Xue Lulu; Zhang Ping; Chen Songzhe; Wang Laijun

2014-01-01

SO_2 depolarized electrolysis (SDE) is the pivotal reaction in hybrid sulfur process, one of the most promising approaches for mass hydrogen production without CO_2 emission. The net result of hybrid sulfur process is to split water into hydrogen and oxygen at a relatively low voltage, which will dramatically decrease the energy consumption for the production of hydrogen. The potential loss of SDE process could be separated into four components, i.e. reversible cell potential, anode overpotential, cathode overpotential and ohmic loss. So far, it has been identified that the total cell potential for the SO_2 depolarized electrolyzer is dominantly controlled by sulfuric acid concentration of the anolyte and electrolysis temperature of the electrolysis process. In this work, an in-situ Electrochemical Impedance Spectroscopy (EIS) measurement of the anodic SDE reaction was conducted. Results show that anodic overpotential is mainly resulted from the SO_2 oxidation reaction other than ohmic resistance or mass transfer limitation. This study extends the understanding to SDE process and gives suggestions for the further improvement of the SDE performance. (author)

Iron dissolution from volcanic ash in low-pH atmospheric water: a key control on volcanic iron input to the surface ocean?

Science.gov (United States)

Maters, E.; Delmelle, P.; Ayris, P. M.; Opfergelt, S.

2012-12-01

A low concentration of dissolved iron (Fe) limits phytoplankton growth in approximately 30% of the ocean. The input of soluble Fe to these High-Nutrient Low-Chlorophyll (HNLC) regions has the potential to boost primary production and thereby enhance the drawdown of atmospheric carbon dioxide (CO2). Over geological timescales, volcanic activity may alter the flux of Fe to the surface ocean and so contribute to modulating atmospheric CO2 concentrations, ultimately impacting the global climate. Ocean Fe fertilisation has also recently been found to contribute to century-scale carbon sequestration via the export of biomass to the seafloor. Atmospherically deposited volcanic ash is now increasingly seen as an intermittent source of Fe to the surface ocean. Understanding the process of Fe release from ash in solution is key for assessing the potential for ash, particularly that produced by large but rare explosive eruptions or during sustained periods of intense volcanism, to fertilise the marine environment. Previous studies have measured the release of Fe from ash in near-neutral pH solution, but the influence of interaction between ash and acidic cloud- or rainwater during transport on Fe release is poorly understood. In this study, seven volcanic ash samples ranging from tephrite to rhyolite (49-74 wt.% SiO2) were leached in pH 1 H2SO4 in batch reactors for 336 h, at a 1:500 ash-to-solution ratio, to investigate Fe release under acidic conditions. Major element concentrations were measured by inductively coupled plasma- atomic emission spectroscopy (ICP-AES) across a time series of ash leachates. Changes in ash surface composition induced by contact with acid solution were assessed by X-ray photoelectron spectroscopy (XPS). The Fe2+/Fe3+ ratio in ash leachates was also determined for the first time, using the Ferrozine method. The ash samples released 42 to 411 μmol m-2 of Fe over 336 h of leaching. High initial Fe release rates (>1 μmol m-2 h-1) sustained for up

Diffuse CO_{2} degassing monitoring of the oceanic active volcanic island of El Hierro, Canary Islands, Spain

Science.gov (United States)

Hernández, Pedro A.; Norrie, Janice; Withoos, Yannick; García-Merino, Marta; Melián, Gladys; Padrón, Eleazar; Barrancos, José; Padilla, Germán; Rodríguez, Fátima; Pérez, Nemesio M.

2017-04-01

one, between October 24 and November 27, 2011, before the most energetic seismic events of the volcanic-seismic unrest (Melián et al., 2014. J. Geophys. Res. Solid Earth, 119, 6976-6991). The highest CO2 degassing rate measured in the last three years (1684 t/d) was observed during a seismo-volcanic unrest. This value decreased until close to background value (˜422 t/d, Melián et al., 2014) contemporaneously with the decline of the seismic activity during the first half of 2013. The last diffuse CO2 degassing survey was carried out in the summer of 2016, showing a emission rate of 854 t/d. Discrete surveys of diffuse CO2 emission have provided important information to optimize the early warning system in the volcano monitoring programs of El Hierro and to monitor the evolution of an ongoing volcanic eruption, even though is a submarine eruption.

A model study of the pollution effects of the first 3 months of the Holuhraun volcanic fissure: comparison with observations and air pollution effects

Directory of Open Access Journals (Sweden)

B. M. Steensen

2016-08-01

Full Text Available The volcanic fissure at Holuhraun, Iceland started at the end of August 2014 and continued for 6 months to the end of February 2015, with an extensive lava flow onto the Holuhraun plain. This event was associated with large SO2 emissions, amounting up to approximately 4.5 times the daily anthropogenic SO2 emitted from the 28 European Union countries, Norway, Switzerland and Iceland. In this paper we present results from EMEP/MSC-W model simulations to which we added 750 kg s−1 SO2 emissions at the Holuhraun plain from September to November (SON, testing three different emission heights. The three simulated SO2 concentrations, weighted with the OMI (Ozone Monitoring Instrument satellite averaging kernel, are found to be within 30 % of the satellite-observed SO2 column burden. Constraining the SO2 column burden with the satellite data while using the kernel along with the three simulated height distributions of SO2, we estimate that the median of the daily burdens may have been between 13 and 40 kt in the North Atlantic area under investigation. We suggest this to be the uncertainty in the satellite-derived burdens of SO2, mainly due to the unknown vertical distribution of SO2. Surface observations in Europe outside Iceland showed concentration increases up to > 500 µg m−3 SO2 from volcanic plumes passing. Three well identified episodes, where the plume crossed several countries, are compared in detail to surface measurements. For all events, the general timing of the observed concentration peaks compared quite well to the model results. The overall changes to the European SO2 budget due to the volcanic fissure are estimated. Three-monthly wet deposition (SON of SOx in the 28 European Union countries, Norway and Switzerland is found to be more than 30 % higher in the model simulation with Holuhraun emissions compared to a model simulation with no Holuhraun emissions. The largest increases, apart from extreme values on

A model study of the pollution effects of the first 3 months of the Holuhraun volcanic fissure: comparison with observations and air pollution effects

Science.gov (United States)

Steensen, Birthe Marie; Schulz, Michael; Theys, Nicolas; Fagerli, Hilde

2016-08-01

The volcanic fissure at Holuhraun, Iceland started at the end of August 2014 and continued for 6 months to the end of February 2015, with an extensive lava flow onto the Holuhraun plain. This event was associated with large SO2 emissions, amounting up to approximately 4.5 times the daily anthropogenic SO2 emitted from the 28 European Union countries, Norway, Switzerland and Iceland. In this paper we present results from EMEP/MSC-W model simulations to which we added 750 kg s-1 SO2 emissions at the Holuhraun plain from September to November (SON), testing three different emission heights. The three simulated SO2 concentrations, weighted with the OMI (Ozone Monitoring Instrument) satellite averaging kernel, are found to be within 30 % of the satellite-observed SO2 column burden. Constraining the SO2 column burden with the satellite data while using the kernel along with the three simulated height distributions of SO2, we estimate that the median of the daily burdens may have been between 13 and 40 kt in the North Atlantic area under investigation. We suggest this to be the uncertainty in the satellite-derived burdens of SO2, mainly due to the unknown vertical distribution of SO2. Surface observations in Europe outside Iceland showed concentration increases up to > 500 µg m-3 SO2 from volcanic plumes passing. Three well identified episodes, where the plume crossed several countries, are compared in detail to surface measurements. For all events, the general timing of the observed concentration peaks compared quite well to the model results. The overall changes to the European SO2 budget due to the volcanic fissure are estimated. Three-monthly wet deposition (SON) of SOx in the 28 European Union countries, Norway and Switzerland is found to be more than 30 % higher in the model simulation with Holuhraun emissions compared to a model simulation with no Holuhraun emissions. The largest increases, apart from extreme values on Iceland, are found on the coast of northern

Volcanic Outgassing and the Rise of Atmospheric O2

Science.gov (United States)

Kasting, J. F.

2012-12-01

The release of reduced volcanic gases played a major role in determining atmospheric composition and redox state during the Earth's Archean era. Along with anerobic iron oxidation during deposition of banded iron-formations (BIFs), volcanic outgassing was one of two major sources of reductants, typically monitored as H2 equivalents, to the early atmosphere. These H2 sources were balanced by sinks of reductants, including escape of hydrogen to space and burial of organic matter and pyrite. The sinks for H2 can alternatively be thought of as sources for O2, following the stoichiometry: 2 H2 + O2 2 H2O. During the Archean, H2 sources were large enough to balance burial of organic matter and pyrite and still allow lots of hydrogen to escape. Sometime close to 2.4 Ga, the redox balance shifted: Either the H2 sources became smaller, or the H2 sinks became larger. The result was that O2 began to accumulate in the atmosphere for the first time, even though it was being produced by cyanobacteria well before this. This allowed a new O2 sink (H2 source) to become operative, namely, oxidative weathering of the land surface and seafloor. On the modern Earth, the redox budget is largely a balance between burial of organic matter and pyrite and oxidative weathering on land. What caused the system to shift to the oxidized state at 2.4 Ga remains a matter of debate. A secular decrease in volcanic outgassing rates alone cannot do this, as organic carbon burial is (loosely) tied to outgassing by the carbon isotope record. Roughly 15-20% of CO2 entering the combined atmosphere-ocean system appears to have been buried as organic carbon; hence, more volcanic outgassing implies more organic carbon burian (and, hence, more O2 production), if everything else stays the same. Other factors were not the same, however. Progressive growth of the continents may have helped O2 to rise, both by changing the ratio of submarine to subaerial outgassing and by facilitating greater recycling of carbon

Critical review of a new volcanic eruption chronology

Science.gov (United States)

Neuhäuser, Dagmar L.; Neuhäuser, Ralph

2016-04-01

Sigl. et al. (2015, Nature) present historical evidence for 32 volcanic eruptions to evaluate their new polar ice core 10-Be chronology - 24 are dated within three years of sulfur layers in polar ice. Most of them can be interpreted as weather phenomena (Babylonia: disk of sun like moon, reported for only one day, e.g. extinction due to clouds), Chinese sunspot reports (pellet, black vapor, etc.), solar eclipses, normal ice-halos and coronae (ring, bow, etc.), one aurora (redness), red suns due to mist drops in wet fog or fire-smoke, etc. Volcanic dust may facilitate detections of sunspots and formation of Bishop's ring, but tend to inhibit ice-halos, which are otherwise often reported in chronicles. We are left with three reports possibly indicating volcanic eruptions, namely fulfilling genuine criteria for atmospheric disturbances due to volcanic dust, e.g. bluish or faint sun, orange sky, or fainting of stars for months (BCE 208, 44-42, and 32). Among the volcanic eruptions used to fix the chronology (CE 536, 626, 939, 1257), the reports cited for the 930s deal only with 1-2 days, at least one reports an eclipse. In the new chronology, there is a sulfur detection eight years after the Vesuvius eruption, but none in CE 79. It may appear surprising that, from BCE 500 to 1, all five northern sulfur peaks labeled in figure 2 in Sigl et al. are systematically later by 2-4 years than the (corresponding?) southern peaks, while all five southern peaks from CE 100 to 600 labeled in figure 2 are systematically later by 1-4 years than the (corresponding?) northern peaks. Furthermore, in most of their six strongest volcanic eruptions, temperatures decreased years before their sulfur dating - correlated with weak solar activity as seen in radiocarbon, so that volcanic climate forcing appears dubious here. Also, their 10-Be peaks at CE 775 and 994 are neither significant nor certain in dating.

Volcanic Ash Cloud Observations with the DLR-Falcon over Europe during Airspace Closure

Science.gov (United States)

Schumann, Ulrich; Weinzierl, Bernadett; Reitebuch, Oliver; Minikin, Andreas; Schlager, Hans; Rahm, Stephan; Scheibe, Monika; Lichtenstern, Michael; Forster, Caroline

2010-05-01

At the time of the EGU conference, the volcano ash plume originating from the Eyjafjallajökull volcano eruption in Iceland was probed during 9 flights with the DLR Falcon research aircraft in the region between Germany and Iceland at 1-11 km altitudes between April 19 and May 3, 2010. The Falcon was instrumented with a downward looking, scanning 2-µm-Wind-Lidar (aerosol backscattering and horizontal wind, 100 m vertical resolution), and several in-situ instruments. The particle instrumentation, including wing station probes (PCASP, FSSP-300) cover particle number and size from 5 nm to some tens of µm. Further in-situ instruments measured O3, CO, SO2, H2O, and standard meteorological parameters. Flight planning was based on numerical weather forecasts, trajectory-based particle-dispersion models, satellite observations and ground based Lidar observations, from many sources. During the flight on April 19, 2010, layers of volcanic ash were detected first by Lidar and then probed in-situ. The horizontal and vertical distribution of the volcanic ash layers over Eastern Germany was highly variable at that time. Calculations with the particle dispersion model FLEXPART indicate that the volcanic ash plumes measured by the Falcon had an age of 4-5 days. The concentrations of large particles measured in the volcanic aerosol layers are comparable to concentrations measured typically in fresh (age 3000 kg/s, strong chemistry - Lidar signal and FSSP-300 signal strongly dependent on refractive index, ash density, particle size spectrum 1- 50 µm - Mid-European airspace closure was justified until Sat. April 17; thereafter ageing ash clouds dominated. - Keflavik/Iceland was found to be free of ash as predicted on April 29 - May 2 - The Quality of forecasts was found to be quite reliable for aviation planning - For the future we recommend combinations of models + lidar + satellite + in-situ - We suggest an improved linking between operations and academia - The DLR Falcon will

Future prices and market for SO2 allowances

International Nuclear Information System (INIS)

Sanghi, A.; Joseph, A.; Michael, K.; Munro, W.; Wang, J.

1993-01-01

The expected price of SO 2 emission allowances is an important issue in energy and integrated resource planning activities. For example, the expected price of SO 2 allowances in needed in order to evaluate alternative strategies for meeting SO 2 provisions of the Clean Air Act Amendments of 1990. In addition, the expected SO 2 allowance price is important to state public utility regulators who must provide guidance on rate-making issues regarding utility compliance plans which involve allowance trading and direct investment of SO 2 control technologies. Last but not the least, the expected SO 2 allowance price is an important determinant of the future market for natural gas and low sulfur coal. The paper develops estimates of SO 2 allowance prices over time by constructing national supply and demand curves for SO 2 reductions. Both the supply and demand for SO 2 reductions are based on an analysis of the sulfur content of fuels burned in 1990 by utilities throughout the United States; and on assumptions about plant retirements, the rate of new capacity growth, the types of new and replacement plants constructed, the costs of SO 2 reduction measures and legislation by midwest states to maintain the use of high sulfur coal to protect local jobs. The paper shows that SO 2 allowance prices will peak around the year 2000 at about $500 per ton, and will eventually fall to zero by about the year 2020. A sensitivity analysis indicates that the price of SO 2 allowances is relatively insensitive to assumptions regarding the availability of natural gas or energy demand growth. However, SO 2 allowance prices tend to be quite sensitive to assumptions regarding regulations which may force early retirement of existing power plants and possible legislation which may reduce CO 2 emissions

Laboratory measurement of the millimeter wave properties of liquid sulfuric acid (H2SO4). [study of microwave emission from Venus

Science.gov (United States)

Fahd, Antoine K.; Steffes, Paul G.

1991-01-01

The methodology and the results of laboratory measurements of the millimeter wave properties of liquid sulfuric acid are presented. Measurements conducted at 30-40 and 90-100 GHz are reported, using different concentrations of liquid H2SO4. The measured data are used to compute the expected opacity of H2SO4 condensates and their effects on the millimeter wave emission from Venus. The cloud condensate is found to have an effect on the emission from Venus. The calculated decrease in brightness temperature is well below the observed decrease in brightness temperature found by de Pater et al. (1991). It is suggested that other constituents such as gaseous H2SO4 also affect the observed variation in the brightness temperature.

Lyman Alpha Camera for Io's SO2 atmosphere and Europa's water plumes

Science.gov (United States)

McEwen, Alfred S.; Sandel, Bill; Schneider, Nick

2014-05-01

The Student Lyman-Alpha Mapper (SLAM) was conceived for the Io Volcano Observer (IVO) mission proposal (McEwen et al., 2014) to determine the spatial and temporal variations in Io's SO2 atmosphere by recording the H Ly-α reflection over the disk (Feldman et al., 2000; Feaga et al., 2009). SO2 absorbs at H Ly-α, thereby modulating the brightness of sunlight reflected by the surface, and measures the density of the SO2 atmosphere and its variability with volcanic activity and time of day. Recently, enhancements at the Ly-α wavelength (121.57 nm) were seen near the limb of Europa and interpreted as active water plumes ~200 km high (Roth et al., 2014). We have a preliminary design for a very simple camera to image in a single bandpass at Ly-α, analogous to a simplified version of IMAGE EUV (Sandel et al. 2000). Our goal is at least 50 resolution elements across Io and/or Europa (~75 km/pixel), ~3x better than HST STIS, to be acquired at a range where the radiation noise is below 1E-4 hits/pixel/s. This goal is achieved with a Cassegrain-like telescope with a 10-cm aperture. The wavelength selection is achieved using a simple self-filtering mirror in combination with a solar-blind photocathode. A photon-counting detector based on a sealed image intensifier preserves the poisson statistics of the incoming photon flux. The intensifier window is coated with a solar-blind photocathode material (CsI). The location of each photon event is recorded by a position-sensitive anode based on crossed delay-line or wedge-and-strip technology. The sensitivity is 0.01 counts/pixel/sec/R, sufficient to estimate SO2 column abundances ranging from 1E15 to 1E17 per cm2 in a 5 min (300 sec) exposure. Sensitivity requirements to search for and image Europa plumes may be similar. Io's Ly-α brightness of ~3 kR exceeds the 0.8 kR brightness of Europa's plume reported by Roth et al. (2014), but the plume brightness is a direct measurement rather than inferring column abundance from

The Use of OMPS Near Real Time Products in Volcanic Cloud Risk Mitigation and Smoke/Dust Air Quality Assessments

Science.gov (United States)

Seftor, C. J.; Krotkov, N. A.; McPeters, R. D.; Li, J. Y.; Durbin, P. B.

2015-12-01

Near real time (NRT) SO2 and aerosol index (AI) imagery from Aura's Ozone Monitoring Instrument (OMI) has proven invaluable in mitigating the risk posed to air traffic by SO2 and ash clouds from volcanic eruptions. The OMI products, generated as part of NASA's Land, Atmosphere Near real-time Capability for EOS (LANCE) NRT system and available through LANCE and both NOAA's NESDIS and ESA's Support to Aviation Control Service (SACS) portals, are used to monitor the current location of volcanic clouds and to provide input into Volcanic Ash (VA) advisory forecasts. NRT products have recently been developed using data from the Ozone Mapping and Profiler Suite onboard the Suomi NPP platform; they are currently being made available through the SACS portal and will shortly be incorporated into the LANCE NRT system. We will show examples of the use of OMPS NRT SO2 and AI imagery to monitor recent volcanic eruption events. We will also demonstrate the usefulness of OMPS AI imagery to detect and track dust storms and smoke from fires, and how this information can be used to forecast their impact on air quality in areas far removed from their source. Finally, we will show SO2 and AI imagery generated from our OMPS Direct Broadcast data to highlight the capability of our real time system.

REAL-TIME MEASUREMENT OF AIRWAY RESPONSES TO SULOFUR DIOXIDE (SO2) IN AN INTACT, AWAKE GUINEA PIG MODEL

Science.gov (United States)

Real-time measurment of airway responses to Sulfur Dioxide (SO2) in an intact, awake guinea pig model. J Stanek1,2, Q Krantz2, J Nolan2, D Winsett2, W Watkinson2, and D Costa2. 1College of Veterinary Medicine, NCSU, Raleigh, NC, USA; 2Pulmonary Toxicology Branch, ETD, NHEERL, US...

Improved optical flow velocity analysis in SO2 camera images of volcanic plumes – implications for emission-rate retrievals investigated at Mt Etna, Italy and Guallatiri, Chile

Directory of Open Access Journals (Sweden)

J. Gliß

2018-02-01

Full Text Available Accurate gas velocity measurements in emission plumes are highly desirable for various atmospheric remote sensing applications. The imaging technique of UV SO2 cameras is commonly used to monitor SO2 emissions from volcanoes and anthropogenic sources (e.g. power plants, ships. The camera systems capture the emission plumes at high spatial and temporal resolution. This allows the gas velocities in the plume to be retrieved directly from the images. The latter can be measured at a pixel level using optical flow (OF algorithms. This is particularly advantageous under turbulent plume conditions. However, OF algorithms intrinsically rely on contrast in the images and often fail to detect motion in low-contrast image areas. We present a new method to identify ill-constrained OF motion vectors and replace them using the local average velocity vector. The latter is derived based on histograms of the retrieved OF motion fields. The new method is applied to two example data sets recorded at Mt Etna (Italy and Guallatiri (Chile. We show that in many cases, the uncorrected OF yields significantly underestimated SO2 emission rates. We further show that our proposed correction can account for this and that it significantly improves the reliability of optical-flow-based gas velocity retrievals. In the case of Mt Etna, the SO2 emissions of the north-eastern crater are investigated. The corrected SO2 emission rates range between 4.8 and 10.7 kg s−1 (average of 7.1  ±  1.3 kg s−1 and are in good agreement with previously reported values. For the Guallatiri data, the emissions of the central crater and a fumarolic field are investigated. The retrieved SO2 emission rates are between 0.5 and 2.9 kg s−1 (average of 1.3  ±  0.5 kg s−1 and provide the first report of SO2 emissions from this remotely located and inaccessible volcano.

The tropospheric processing of acidic gases and hydrogen sulphide in volcanic gas plumes as inferred from field and model investigations

Directory of Open Access Journals (Sweden)

A. Aiuppa

2007-01-01

variations in the modelled SO2/HCl ratios were predicted under cloudy conditions, due to heterogeneous chlorine cycling in the aerosol phase. The modelled evolution of the SO2/H2S ratios is found to be substantially dependent on whether or not the interactions of H2S with halogens are included in the model. In the former case, H2S is assumed to be oxidized in the atmosphere mainly by OH, which results in minor chemical loss for H2S during plume aging and produces a fair match between modelled and measured SO2/H2S ratios. In the latter case, fast oxidation of H2S by Cl leads to H2S chemical lifetimes in the early plume of a few seconds, and thus SO2 to H2S ratios that increase sharply during plume transport. This disagreement between modelled and observed plume compositions suggests that more in-detail kinetic investigations are required for a proper evaluation of H2S chemical processing in volcanic plumes.

Surface Hydrophobicity Causes SO2 Tolerance in Lichens

Science.gov (United States)

Hauck, Markus; Jürgens, Sascha-René; Brinkmann, Martin; Herminghaus, Stephan

2008-01-01

Background and Aims The superhydrophobicity of the thallus surface in one of the most SO2-tolerant lichen species, Lecanora conizaeoides, suggests that surface hydrophobicity could be a general feature of lichen symbioses controlling their tolerance to SO2. The study described here tests this hypothesis. Methods Water droplets of the size of a raindrop were placed on the surface of air-dry thalli in 50 lichen species of known SO2 tolerance and contact angles were measured to quantify hydrophobicity. Key Results The wettability of lichen thalli ranges from strongly hydrophobic to strongly hydrophilic. SO2 tolerance of the studied lichen species increased with increasing hydrophobicity of the thallus surface. Extraction of extracellular lichen secondary metabolites with acetone reduced, but did not abolish the hydrophobicity of lichen thalli. Conclusions Surface hydrophobicity is the main factor controlling SO2 tolerance in lichens. It presumably originally evolved as an adaptation to wet habitats preventing the depression of net photosynthesis due to supersaturation of the thallus with water. Hydrophilicity of lichen thalli is an adaptation to dry or humid, but not directly rain-exposed habitats. The crucial role of surface hydrophobicity in SO2 also explains why many markedly SO2-tolerant species are additionally tolerant to other (chemically unrelated) toxic substances including heavy metals. PMID:18077467

Volcanic Eruptions and Climate

Science.gov (United States)

LeGrande, Allegra N.; Anchukaitis, Kevin J.

2015-01-01

Volcanic eruptions represent some of the most climatically important and societally disruptive short-term events in human history. Large eruptions inject ash, dust, sulfurous gases (e.g. SO2, H2S), halogens (e.g. Hcl and Hbr), and water vapor into the Earth's atmosphere. Sulfurous emissions principally interact with the climate by converting into sulfate aerosols that reduce incoming solar radiation, warming the stratosphere and altering ozone creation, reducing global mean surface temperature, and suppressing the hydrological cycle. In this issue, we focus on the history, processes, and consequences of these large eruptions that inject enough material into the stratosphere to significantly affect the climate system. In terms of the changes wrought on the energy balance of the Earth System, these transient events can temporarily have a radiative forcing magnitude larger than the range of solar, greenhouse gas, and land use variability over the last millennium. In simulations as well as modern and paleoclimate observations, volcanic eruptions cause large inter-annual to decadal-scale changes in climate. Active debates persist concerning their role in longer-term (multi-decadal to centennial) modification of the Earth System, however.

Phase formation in the systems ZrO2-H2SO4-Na2SO4 (NaCl)-H2O

International Nuclear Information System (INIS)

Sozinova, Yu.P.; Motov, D.L.; Rys'kina, M.P.

1988-01-01

Formation of solid phases in the systems ZrO 2 - H 2 SO 4 - Na 2 SO 4 (NaCl) - H 2 O at 25 and 75 deg C is studied. Three basic Na 2 Zr(OH) 2 (SO 4 ) 2 x (0.2 - 0.4)H 2 O, NaZrOH(SO 4 ) 2 x H 2 O, NaZrO 0.5 (OH) 2 SO 4 x 2H 2 O and three normal sodium sulfatozirconates Na 2 Zr(SO 4 ) 3 x 3H 2 O, Na 4 Zr(SO 4 ) 4 x 3H 2 O, Na 6 Zr(SO 4 ) 5 x 4H 2 O have been isolated, their solubility and crystal optical properties are determined

Factorizable S-matrix for SO(D)/SO(2) circle times SO(D - 2) non-linear σ models with fermions

International Nuclear Information System (INIS)

Abdalla, E.; Lima-Santos, A.

1988-01-01

The authors compute the exact S matrix for the non-linear sigma model with symmetry SO(D)/SO(2) circle times SO(D-2) coupled to fermions in a minimal or supersymmetric way. The model has some relevance in string theory with non-zero external curvature

Volcanic Eruption Observations from an Elevated Point of the Stromboli Using Thermal Infrared Hyperspectral Imaging

Science.gov (United States)

Morton, V.; Gagnon, M. A.; Marcotte, F.; Gouhier, M.; Smekens, J. F.

2017-12-01

Many urban areas are located near active volcanoes around the world. Therefore, scientific research on different indicators of imminent eruptions is carried out on an ongoing basis. Due to the hazardous and unpredictable behavior of volcanoes, remote sensing technologies are normally preferred for investigations. Over the years, the Telops Hyper-Cam, a high-performance infrared hyperspectral camera, has established itself as a reference tool for investigating gas clouds over large distances. In order to illustrate the benefits of standoff infrared hyperspectral imaging for characterizing volcanic processes, many different measurements were carried out from an elevated point ( 800 m) of the Stromboli volcano (Italy) by researchers from the Université Blaise-Pascal (Clermont-Ferrand, France). The Stromboli volcano is well known for its periodic eruptions of small magnitude containing various proportions of ash, lava and gases. Imaging was carried out at a relatively high spectral and spatial resolution before and during eruptions from the North-East (NE) craters. Both sulfur dioxide (SO2) and sulfur tetrafluoride (SiF4) could be successfully identified within the volcano's plume from their distinct spectral features. During the passive degassing phase, a total amount of 3.3 kg of SO2 and 0.8 g of SiF4 were estimated. A violent eruption from NE1 crater was then observed and a total of 45 g and and 7 g of SO2 and SiF4 were estimated respectively. These results are in good agreement with previous work using a UV-SO2 camera. Finally, a smaller eruption from NE2 crater was observed. Total amounts of 3 kg and 17 g of SO2 and SiF4 were estimated respectively. Quantitative chemical maps for both gases will be presented. The results show that standoff thermal infrared hyperspectral imaging provides unique insights for a better understanding of volcanic eruptions.

CO2 flux from Javanese mud volcanism.

Science.gov (United States)

Queißer, M; Burton, M R; Arzilli, F; Chiarugi, A; Marliyani, G I; Anggara, F; Harijoko, A

2017-06-01

Studying the quantity and origin of CO 2 emitted by back-arc mud volcanoes is critical to correctly model fluid-dynamical, thermodynamical, and geochemical processes that drive their activity and to constrain their role in the global geochemical carbon cycle. We measured CO 2 fluxes of the Bledug Kuwu mud volcano on the Kendeng Fold and thrust belt in the back arc of Central Java, Indonesia, using scanning remote sensing absorption spectroscopy. The data show that the expelled gas is rich in CO 2 with a volume fraction of at least 16 vol %. A lower limit CO 2 flux of 1.4 kg s -1 (117 t d -1 ) was determined, in line with the CO 2 flux from the Javanese mud volcano LUSI. Extrapolating these results to mud volcanism from the whole of Java suggests an order of magnitude total CO 2 flux of 3 kt d -1 , comparable with the expected back-arc efflux of magmatic CO 2 . After discussing geochemical, geological, and geophysical evidence we conclude that the source of CO 2 observed at Bledug Kuwu is likely a mixture of thermogenic, biogenic, and magmatic CO 2 , with faulting controlling potential pathways for magmatic fluids. This study further demonstrates the merit of man-portable active remote sensing instruments for probing natural gas releases, enabling bottom-up quantification of CO 2 fluxes.

Lidar observations of stratospheric aerosol layer after the Mt. Pinatubo volcanic eruption

International Nuclear Information System (INIS)

Nagai, Tomohiro; Uchino, Osamu; Fujimoto, Toshifumi.

1992-01-01

The volcano Mt. Pinatubo located on the Luzon Island, Philippines, had explosively erupted on June 15, 1991. The volcanic eruptions such as volcanic ash, SO2 and H2O reached into the stratosphere over 30 km altitude by the NOAA-11 satellite observation and this is considered one of the biggest volcanic eruptions in this century. A grandiose volcanic eruption influences the atmosphere seriously and causes many climatic effects globally. There had been many impacts on radiation, atmospheric temperature and stratospheric ozone after some past volcanic eruptions. The main cause of volcanic influence depends on stratospheric aerosol, that stay long enough to change climate and other meteorological conditions. Therefore it is very important to watch stratospheric aerosol layers carefully and continuously. Standing on this respect, we do not only continue stratospheric aerosol observation at Tsukuba but also have urgently developed another lidar observational point at Naha in Okinawa Island. This observational station could be thought valuable since there is no lidar observational station in this latitudinal zone and it is much nearer to Mt. Pinatubo. Especially, there is advantage to link up these two stations on studying the transportation mechanism in the stratosphere. In this paper, we present the results of lidar observations at Tsukuba and Naha by lidar systems with Nd:YAG laser

Lidar Observations of Stratospheric Aerosol Layer After the Mt. Pinatubo Volcanic Eruption

Science.gov (United States)

Nagai, Tomohiro; Uchino, Osamu; Fujimoto, Toshifumi

1992-01-01

The volcano Mt. Pinatubo located on the Luzon Island, Philippines, had explosively erupted on June 15, 1991. The volcanic eruptions such as volcanic ash, SO2 and H2O reached into the stratosphere over 30 km altitude by the NOAA-11 satellite observation and this is considered one of the biggest volcanic eruptions in this century. A grandiose volcanic eruption influences the atmosphere seriously and causes many climatic effects globally. There had been many impacts on radiation, atmospheric temperature and stratospheric ozone after some past volcanic eruptions. The main cause of volcanic influence depends on stratospheric aerosol, that stay long enough to change climate and other meteorological conditions. Therefore it is very important to watch stratospheric aerosol layers carefully and continuously. Standing on this respect, we do not only continue stratospheric aerosol observation at Tsukuba but also have urgently developed another lidar observational point at Naha in Okinawa Island. This observational station could be thought valuable since there is no lidar observational station in this latitudinal zone and it is much nearer to Mt. Pinatubo. Especially, there is advantage to link up these two stations on studying the transportation mechanism in the stratosphere. In this paper, we present the results of lidar observations at Tsukuba and Naha by lidar systems with Nd:YAG laser.

Study of ZrO2-H2SO4-(NH4)2SO4(NH4Cl)-H2O systems

International Nuclear Information System (INIS)

Motov, D.L.; Sozinova, Yu.P.; Rys'kina, M.P.

1988-01-01

Regions of formation, composition and solubility of ammonium sulfatozirconates (ASZ) in ZrO 2 -H 2 SO 4 -(NH 4 ) 2 SO 4 (NH 4 Cl)-H 2 O systems at 25 and 75 deg C are studied by the isothermal method. Five ASZ: (NH 4 ) 2 Zr(OH) 2 (SO 4 ) 2 , NH 4 ZrOH(SO 4 ) 2 xH 2 O, NH 4 ZrO 0.5 (OH) 2 SO 4 x1.5H 2 O, (NH 4 ) 2 Zr(SO 4 ) 3 x2H 2 O, (NH 4 ) 4 Zr(SO 4 ) 4 x4H 2 O are detected, their properties are investigated. Main sulfates are new compounds never described ealier

Volcanism in the Sumisu Rift. Pt. 2

International Nuclear Information System (INIS)

Hochstaedter, A.G.; Gill, J.B.; Morris, J.D.

1990-01-01

A bimodal suite of volcanic rocks collected from the Sumisu Rift by ALVIN provide present day example of the first magmatic products of arc rifting during the initiation of back-arc spreading. The trace element and isotopic composition of these rocks, which are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, differ from those of arc rocks and N-MORB in their relative incorporation of both subduction-related and non-subduction-related components. Subduction-related components, i.e., those that distinguish volcanic arc basalts from N-MORB, are less pronounced in rift lavas than in arc lavas. Alkali and alkaline earth to high field strength element and REE ratios as well as 87 Sr/ 86 Sr are intermediate between those of N-MORB and Izu arc lavas and indicate that Sumisu Rift basalts are similar to BABB erupted in other, more mature back-arc basins. These results show that back-arc basins may begin their magmatic evolution with BABB rather than more arc-like lavas. Evidence of non-subduction related components remains after the effects of subduction related components are removed or accounted for. Compared to the arc, higher HFSE and REE concentrations, contrasting REE patterns, and ≤ε Nd in the rift reflect derivation of rift lavas from more enriched components. Although SR basalt resembles E-MORB in many trace element ratios, it is referred to as BABB because low concentrations of Nb are similar to those in volcanic arcs and H 2 O/REE and H 2 O/K 2 O exceed those of E-MORB. Differences in HREE pattern and ε Nd require that the E-MORB characteristics result from source heterogeneities and not lower degrees of melting. Enriched mantle beneath the rift may reflect enriched blobs entrained in a more depleted matrix, or injection of new, more enriched mantle. High 208 Pb/ 204 Pb and moderate 207 Pb/ 204 Pb ratios with respect to Pacific MORB also reflect ancient mantle enrichment. (orig.)

Production of low molecular weight hydrocarbons by volcanic eruptions on early Mars.

Science.gov (United States)

Segura, Antígona; Navarro-González, Rafael

2005-10-01

Methane and other larger hydrocarbons have been proposed as possible greenhouse gases on early Mars. In this work we explore if volcanic processes may have been a source for such molecules based on theoretical and experimental considerations. Geologic evidence and numerical simulations indicate that explosive volcanism was widely distributed throughout Mars. Volcanic lightning is typically produced in such explosive volcanism. Therefore this geologic setting was studied to determine if lightning could be a source for hydrocarbons in volcanic plumes. Volcanic lightning was simulated by focusing a high-energy infrared laser beam inside of a Pyrex reactor that contained the proposed volcanic gas mixture composed of 64% CH(4), 24% H(2), 10% H(2)O and 2% N(2), according to an accretion model and the nitrogen content measured in Martian meteorites. The analysis of products was performed by gas chromatography coupled to infrared and mass spectroscopy. Eleven hydrocarbons were identified among the products, of which acetylene (C(2)H(2)) was the most abundant. A thermochemical model was used to determine which hydrocarbons could arise only from volcanic heat. In this case, acetylene and ethylene are formed at magmatic temperatures. Our results indicate that explosive volcanism may have injected into the atmosphere of early Mars approximately 6 x 10(12) g yr(-1) of acetylene, and approximately 2 x 10(12) g yr(-1) of 1,3-butadiyne, both produced by volcanic lightning, approximately 5 x 10(11) g yr(-1) of ethylene produced by volcanic heat, and 10(13) g yr(-1) of methane.

Age of the Auckland Volcanic Field

International Nuclear Information System (INIS)

Lindsay, J.; Leonard, G.S.

2009-01-01

In 2008 a multi-disciplinary research programme was launched, a GNS Science-University of Auckland collaboration with the aim of DEtermining VOlcanic Risk in Auckland (DEVORA). A major aspiration of DEVORA is development of a probabilistic hazard model for the Auckland Volcanic Field (AVF). This will be achieved by investigating past eruption magnitude-frequency relationships and comparing these with similar data from analogous volcanic fields. A key data set underpinning this is an age database for the AVF. To this end a comprehensive dating campaign is planned as part of DEVORA. This report, Age of the Auckland Volcanic Field, is a synthesis of all currently available age data for the AVF. It represents one of several reports carried out as part of the 'synthesis' phase of DEVORA, whereby existing data from all previous work is collated and summarised, so that gaps in current knowledge can be identified and addressed. (author). 60 refs., 7 figs., 31 tabs.

Radiative and Dynamical Feedbacks Limit the Climate Response to Extremely Large Volcanic Eruptions

Science.gov (United States)

Wade, D. C.; Vidal, C. M.; Keeble, J. M.; Griffiths, P. T.; Archibald, A. T.

2017-12-01

Explosive volcanic eruptions are a major cause of chemical and climatic perturbations to the atmosphere, injecting chemically and radiatively active species such as sulfur dioxide (SO2) into the stratosphere. The rate determining step for sulfate aerosol production is SO2 + OH +M → HSO3 +M. This means that chemical feedbacks on the hydroxyl radical, OH, can modulate the production rate of sulfate aerosol and hence the climate effects of large volcanic eruptions. Radiative feedbacks due to aerosols, ozone and sulfur dioxide and subsequent dynamical changes also affect the evolution of the aerosol cloud. Here we assess the role of radiative and chemical feedbacks on sulfate aerosol production using UM-UKCA, a chemistry-climate model coupled to GLOMAP, a prognostic modal aerosol model. A 200 Tg (10x Pinatubo) emission scenario is investigated. Accounting for radiative feedbacks, the SO2 lifetime is 55 days compared to 26 days in the baseline 20 Tg (1x Pinatubo) simulation. By contrast, if all radiative feedbacks are neglected the lifetime is 73 days. Including radiative feedbacks reduces the SO2 lifetime: heating of the lower stratosphere by aerosol increases upwelling and increases transport of water vapour across the tropopause, increasing OH concentrations. The maximum effective radius of the aerosol particles increases from 1.09 µm to 1.34 µm as the production of aerosol is quicker. Larger and fewer aerosol particles are produced which are less effective at scattering shortwave radiation and will more quickly sediment from the stratosphere. As a result, the resulting climate cooling by the eruption will be less strong when accounting for these radiative feedbacks. We illustrate the consequences of these effects for the 1257 Samalas eruption, the largest common era volcanic eruption, using UM-UKCA in a coupled atmosphere-ocean configuration. As a potentially halogen rich eruption, we investigate the differing ozone response to halogen-rich and halogen

Hydrothermal Solute Flux from Ebeko Volcanic Center, Paramushir, Kuril Islands

Science.gov (United States)

Taran, Y.; Kalacheva, E.; Kotenko, T.; Chaplygin, I.

2014-12-01

Ebeko volcano on the northern part of Paramushir Island, Northern Kurils, is characterized by frequent phreatic eruptions, a strong low-temperature fumarolic activity at the summit and was the object of comprehensive volcanological and geochemical studies during the last half a century. The volcanic center is composed of several Pleistocene volcanic structures aadjacent to Ebeko and hosts a hydrothermal system with a high outflow rate of hot SO4-Cl acidic water (Upper Yurieva springs) with the current maximum temperature of ~85oC, pH 1.3 and TDS ~ 10 g/L. All discharging thermal waters are drained by the Yurieva River to the Sea of Okhotsk. The hot springs have been changing in time, generally decreasing their activity from near boiling in 1960s, with TDS ~ 20 g/L and the presence of a small steaming field at the upper part of the ~ 700 m long discharging area, to a much lower discharge rate of main vents, lower temperature and the absence of the steaming ground. The spring chemistry did not react to the Ebeko volcanic activity (14 strong phreato-magmatic events during the last 60 years).The total measured outputs of chloride and sulfur from the system last time (2006-2010) were estimated on average as 730 g/s and 980 g/s, respectively, which corresponds to the equivalent fluxes of 64 t/d of HCl and 169 t/d of SO2. These values are higher than the fumarolic volatile output from Ebeko. The estimated discharge rate of hot (85oC) water from the system with ~ 3500 ppm of chloride is about 0.3 m3/s which is much higher than the thermal water discharge from El Chichon or Copahue volcano-hydrothermal systems and among the highest hot water natural outputs ever measured for a volcano-hydrothermal system. We also report the chemical composition (major and ~ 60 trace elements including REE) of water from the main hot spring vents and the Yurieva river mouth.

Exploring the atmospheric chemistry of O2SO3- and assessing the maximum turnover number of ion-catalysed H2SO4 formation

DEFF Research Database (Denmark)

Bork, Nicolai Christian; Kurtén, T.; Vehkamäki, H.

2013-01-01

molecule, but reaction (b) is in general much more probable. Although we are unable to assess the overall importance of this cycle in the real atmosphere due to the unknown influence of CO2 and NOx, we roughly estimate that ion-induced catalysis may contribute with several percent of H2SO4 levels......It has recently been demonstrated that the O2SO3- ion forms in the atmosphere as a natural consequence of ionizing radiation. Here, we present a density functional theory-based study of the reactions of O2SO3- with O-3. The most important reactions are (a) oxidation to O3SO3- and (b) cluster...... the two major sinks for O2SO3- is assessed, thereby providing a measure of the maximum turnover number of ion-catalysed SO2 oxidation, i.e. how many SO2 can be oxidized per free electron. The rate ratio between reactions (a) and (b) is significantly altered by the presence or absence of a single water...

Chemistry of ash-leachates to monitor volcanic activity: An application to Popocatepetl volcano, central Mexico

Energy Technology Data Exchange (ETDEWEB)

Armienta, M.A., E-mail: victoria@geofisica.unam.mx [Universidad Nacional Autonoma de Mexico, Instituto de Geofisica, Circuito Exterior, C.U., Mexico 04510 D.F. (Mexico); De la Cruz-Reyna, S. [Universidad Nacional Autonoma de Mexico, Instituto de Geofisica, Circuito Exterior, C.U., Mexico 04510 D.F. (Mexico); Soler, A. [Grup de Mineralogia Aplicada i Medi Ambient, Dep. Cristal.lografia, Mineralogia i Diposits Minerals, Fac. Geologia, Universidad de Barcelona (Spain); Cruz, O.; Ceniceros, N.; Aguayo, A. [Universidad Nacional Autonoma de Mexico, Instituto de Geofisica, Circuito Exterior, C.U., Mexico 04510 D.F. (Mexico)

2010-08-15

Monitoring volcanic activity and assessing volcanic risk in an on-going eruption is a problem that requires the maximum possible independent data to reduce uncertainty. A quick, relatively simple and inexpensive method to follow the development of an eruption and to complement other monitoring parameters is the chemical analysis of ash leachates, particularly in the case of eruptions related to dome emplacement. Here, the systematic analysis of SO{sub 4}{sup 2-}, Cl{sup -} and F{sup -} concentrations in ash leachates is proposed as a valuable tool for volcanic activity monitoring. However, some results must be carefully assessed, as is the case for S/Cl ratios, since eruption of hydrothermally altered material may be confused with degassing of incoming magma. Sulfur isotopes help to identify SO{sub 4} produced by hydrothermal processes from magmatic SO{sub 2}. Lower S isotopic values correlated with higher F{sup -} percentages represent a better indicator of fresh magmatic influence that may lead to stronger eruptions and emplacement of new lava domes. Additionally, multivariate statistical analysis helps to identify different eruption characteristics, provided that the analyses are made over a long enough time to sample different stages of an eruption.

Chemistry of ash-leachates to monitor volcanic activity: An application to Popocatepetl volcano, central Mexico

International Nuclear Information System (INIS)

Armienta, M.A.; De la Cruz-Reyna, S.; Soler, A.; Cruz, O.; Ceniceros, N.; Aguayo, A.

2010-01-01

Monitoring volcanic activity and assessing volcanic risk in an on-going eruption is a problem that requires the maximum possible independent data to reduce uncertainty. A quick, relatively simple and inexpensive method to follow the development of an eruption and to complement other monitoring parameters is the chemical analysis of ash leachates, particularly in the case of eruptions related to dome emplacement. Here, the systematic analysis of SO 4 2- , Cl - and F - concentrations in ash leachates is proposed as a valuable tool for volcanic activity monitoring. However, some results must be carefully assessed, as is the case for S/Cl ratios, since eruption of hydrothermally altered material may be confused with degassing of incoming magma. Sulfur isotopes help to identify SO 4 produced by hydrothermal processes from magmatic SO 2 . Lower S isotopic values correlated with higher F - percentages represent a better indicator of fresh magmatic influence that may lead to stronger eruptions and emplacement of new lava domes. Additionally, multivariate statistical analysis helps to identify different eruption characteristics, provided that the analyses are made over a long enough time to sample different stages of an eruption.

Study of structural change in volcanic and geothermal areas using seismic tomography

Science.gov (United States)

Mhana, Najwa; Foulger, Gillian; Julian, Bruce; peirce, Christine

2014-05-01

Long Valley caldera is a large silicic volcano. It has been in a state of volcanic and seismic unrest since 1978. Farther escalation of this unrest could pose a threat to the 5,000 residents and the tens of thousands of tourists who visit the area. We have studied the crustal structure beneath 28 km X 16 km area using seismic tomography. We performed tomographic inversions for the years 2009 and 2010 with a view to differencing it with the 1997 result to look for structural changes with time and whether repeat tomography is a capable of determining the changes in structure in volcanic and geothermal reservoirs. Thus, it might provide a useful tool to monitoring physical changes in volcanoes and exploited geothermal reservoirs. Up to 600 earthquakes, selected from the best-quality events, were used for the inversion. The inversions were performed using program simulps12 [Thurber, 1983]. Our initial results show that changes in both V p and V s were consistent with the migration of CO2 into the upper 2 km or so. Our ongoing work will also invert pairs of years simultaneously using a new program, tomo4d [Julian and Foulger, 2010]. This program inverts for the differences in structure between two epochs so it can provide a more reliable measure of structural change than simply differencing the results of individual years.

Vertical profiles for SO2 and SO on Venus from different one-dimensional simulations

Science.gov (United States)

Mills, Franklin P.; Jessup, Kandis-Lea; Yung, Yuk

2017-10-01

Sulfur dioxide (SO2) plays many roles in Venus’ atmosphere. It is a precursor for the sulfuric acid that condenses to form the global cloud layers and is likely a precursor for the unidentified UV absorber, which, along with CO2 near the tops of the clouds, appears to be responsible for absorbing about half of the energy deposited in Venus’ atmosphere [1]. Most published simulations of Venus’ mesospheric chemistry have used one-dimensional numerical models intended to represent global-average or diurnal-average conditions [eg, 2, 3, 4]. Observations, however, have found significant variations of SO and SO2 with latitude and local time throughout the mesosphere [eg, 5, 6]. Some recent simulations have examined local time variations of SO and SO2 using analytical models [5], one-dimensional steady-state solar-zenith-angle-dependent numerical models [6], and three-dimensional general circulation models (GCMs) [7]. As an initial step towards a quantitative comparison among these different types of models, this poster compares simulated SO, SO2, and SO/SO2 from global-average, diurnal-average, and solar-zenith-angle (SZA) dependent steady-state models for the mesosphere.The Caltech/JPL photochemical model [8] was used with vertical transport via eddy diffusion set based on observations and observationally-defined lower boundary conditions for HCl, CO, and OCS. Solar fluxes are based on SORCE SOLSTICE and SORCE SIM measurements from 26 December 2010 [9, 10]. The results indicate global-average and diurnal-average models may have significant limitations when used to interpret latitude- and local-time-dependent observations of SO2 and SO.[1] Titov D et al (2007) in Exploring Venus as a Terrestrial Planet, 121-138. [2] Zhang X et al (2012) Icarus, 217, 714-739. [3] Krasnopolsky V A (2012) Icarus, 218, 230-246. [4] Parkinson C D et al (2015) Planet Space Sci, 113-114, 226-236. [5] Sandor B J et al (2010) Icarus, 208, 49-60. [6] Jessup K-L et al (2015) Icarus, 258, 309

Next Generation Aura-OMI SO2 Retrieval Algorithm: Introduction and Implementation Status

Science.gov (United States)

Li, Can; Joiner, Joanna; Krotkov, Nickolay A.; Bhartia, Pawan K.

2014-01-01

We introduce our next generation algorithm to retrieve SO2 using radiance measurements from the Aura Ozone Monitoring Instrument (OMI). We employ a principal component analysis technique to analyze OMI radiance spectral in 310.5-340 nm acquired over regions with no significant SO2. The resulting principal components (PCs) capture radiance variability caused by both physical processes (e.g., Rayleigh and Raman scattering, and ozone absorption) and measurement artifacts, enabling us to account for these various interferences in SO2 retrievals. By fitting these PCs along with SO2 Jacobians calculated with a radiative transfer model to OMI-measured radiance spectra, we directly estimate SO2 vertical column density in one step. As compared with the previous generation operational OMSO2 PBL (Planetary Boundary Layer) SO2 product, our new algorithm greatly reduces unphysical biases and decreases the noise by a factor of two, providing greater sensitivity to anthropogenic emissions. The new algorithm is fast, eliminates the need for instrument-specific radiance correction schemes, and can be easily adapted to other sensors. These attributes make it a promising technique for producing long-term, consistent SO2 records for air quality and climate research. We have operationally implemented this new algorithm on OMI SIPS for producing the new generation standard OMI SO2 products.

Distribution of sulfur aerosol precursors in the SPCZ released by continuous volcanic degassing at Ambrym, Vanuatu

Science.gov (United States)

Lefèvre, Jérôme; Menkes, Christophe; Bani, Philipson; Marchesiello, Patrick; Curci, Gabriele; Grell, Georg A.; Frouin, Robert

2016-08-01

The Melanesian Volcanic Arc (MVA) emits about 12 kT d- 1 of sulfur dioxide (SO2) to the atmosphere from continuous passive (non-explosive) volcanic degassing, which contributes 20% of the global SO2 emission from volcanoes. Here we assess, from up-to-date and long-term observations, the SO2 emission of the Ambrym volcano, one of the dominant volcanoes in the MVA, and we investigate its role as sulfate precursor on the regional distribution of aerosols, using both satellite observations and model results at 1° × 1° spatial resolution from WRF-Chem/GOCART. Without considering aerosol forcing on clouds, our model parameterizations for convection, vertical mixing and cloud properties provide a reliable chemical weather representation, making possible a cross-examination of model solution and observations. This preliminary work enables the identification of biases and limitations affecting both the model (missing sources) and satellite sensors and algorithms (for aerosol detection and classification) and leads to the implementation of improved transport and aerosol processes in the modeling system. On the one hand, the model confirms a 50% underestimation of SO2 emissions due to satellite swath sampling of the Ozone Monitoring Instrument (OMI), consistent with field studies. The OMI irregular sampling also produces a level of noise that impairs its monitoring capacity during short-term volcanic events. On the other hand, the model reveals a large sensitivity on aerosol composition and Aerosol Optical Depth (AOD) due to choices of both the source function in WRF-Chem and size parameters for sea-salt in FlexAOD, the post-processor used to compute offline the simulated AOD. We then proceed to diagnosing the role of SO2 volcanic emission in the regional aerosol composition. The model shows that both dynamics and cloud properties associated with the South Pacific Convergence Zone (SPCZ) have a large influence on the oxidation of SO2 and on the transport pathways of

An overview of the Icelandic Volcano Observatory response to the on-going rifting event at Bárðarbunga (Iceland) and the SO2 emergency associated with the gas-rich eruption in Holuhraun

Science.gov (United States)

Barsotti, Sara; Jonsdottir, Kristin; Roberts, Matthew J.; Pfeffer, Melissa A.; Ófeigsson, Benedikt G.; Vögfjord, Kristin; Stefánsdóttir, Gerður; Jónasdóttir, Elin B.

2015-04-01

On 16 August, 2014, Bárðarbunga volcano entered a new phase of unrest. Elevated seismicity in the area with up to thousands of earthquakes detected per day and significant deformation was observed around the Bárðarbunga caldera. A dike intrusion was monitored for almost two weeks until a small, short-lived effusive eruption began on 29 August in Holuhraun. Two days later a second, more intense, tremendously gas-rich eruption started that is still (as of writing) ongoing. The Icelandic Volcano Observatory (IVO), within the Icelandic Meteorological Office (IMO), monitors all the volcanoes in Iceland. Responsibilities include evaluating their related hazards, issuing warnings to the public and Civil Protection, and providing information regarding risks to aviation, including a weekly summary of volcanic activity provided to the Volcanic Ash Advisory Center in London. IVO has monitored the Bárðarbunga unrest phase since its beginning with the support of international colleagues and, in collaboration with the University of Iceland and the Environment Agency of Iceland, provides scientific support and interpretation of the ongoing phenomena to the local Civil Protection. The Aviation Color Code, for preventing hazards to aviation due to ash-cloud encounter, has been widely used and changed as soon as new observations and geophysical data from the monitoring network have suggested a potential evolution in the volcanic crisis. Since the onset of the eruption, IVO is monitoring the gas emission by using different and complementary instrumentations aimed at analyzing the plume composition as well as estimating the gaseous fluxes. SO2 rates have been measured with both real-time scanning DOASes and occasional mobile DOAS traveses, near the eruption site and in the far field. During the first month-and-a-half of the eruption, an average flux equal to 400 kg/s was registered, with peaks exceeding 1,000 kg/s. Along with these measurements the dispersal model CALPUFF has

Lahar—River of volcanic mud and debris

Science.gov (United States)

Major, Jon J.; Pierson, Thomas C.; Vallance, James W.

2018-05-09

Lahar, an Indonesian word for volcanic mudflow, is a mixture of water, mud, and volcanic rock flowing swiftly along a channel draining a volcano. Lahars can form during or after eruptions, or even during periods of inactivity. They are among the greatest threats volcanoes pose to people and property. Lahars can occur with little to no warning, and may travel great distances at high speeds, destroying or burying everything in their paths.Lahars form in many ways. They commonly occur when eruptions melt snow and ice on snow-clad volcanoes; when rains fall on steep slopes covered with fresh volcanic ash; when crater lakes, volcano glaciers or lakes dammed by volcanic debris suddenly release water; and when volcanic landslides evolve into flowing debris. Lahars are especially likely to occur at erupting or recently active volcanoes.Because lahars are so hazardous, U.S. Geological Survey scientists pay them close attention. They study lahar deposits and limits of inundation, model flow behavior, develop lahar-hazard maps, and work with community leaders and governmental authorities to help them understand and minimize the risks of devastating lahars.

Volcanic glass signatures in spectroscopic survey of newly proposed lunar pyroclastic deposits

Science.gov (United States)

Besse, S.; Sunshine, J.M.; Gaddis, L.R.

2014-01-01

Moon Mineralogy Mapper spectroscopic observations are used to assess the mineralogy of five sites that have recently been proposed to include lunar dark mantle deposits (DMDs). Volcanic glasses have, for the first time, clearly been identified at the location of three of the proposed pyroclastic deposits. This is the first time that volcanic glasses have been identified at such a small scale on the lunar surface from remote sensing observations. Deposits at Birt E, Schluter, and Walther A appear to be glassy DMDs. Deposits at Birt E and Schluter show (1) morphological evidence suggesting a likely vent and (2) mineralogical evidence indicative of the presence of volcanic glasses. The Walther A deposits, although they show no morphological evidence of vents, have the spectroscopic characteristics diagnostic of volcanic glasses. The deposits of the Freundlich-Sharonov basin are separated in two areas: (1) the Buys-Ballot deposits lack mineralogical and morphological evidence and thus are found to be associated with mare volcanism not with DMDs and (2) the Anderson crater deposits, which do not exhibit glassy DMD signatures, but they appear to be associated with possible vent structures and so may be classifiable as DMDs. Finally, dark deposits near the crater Kopff are found to be associated with likely mare volcanism and not associated with DMDs. The spectral identification of volcanic glass seen in many of the potential DMDs is a strong indicator of their pyroclastic origin.

Dispersion capacitive de l'interface H 2 SO 4 /Pt | Hammadi ...

African Journals Online (AJOL)

Capacitive dispersion of Pt/H2SO4 interface. Impedance measurements by EIS and voltammograms measurements by CV on pretreated Pt electrodes immersed in an electrolytic solution of 0.5M H2SO4 are presented. Two electrochemical pretreatment techniques of the WE (thin Pt wire) are used: cleaning and etching.

Volcanic activity in the Acambay Graben: a < 25 Ka subplinian eruption from the Temascalcingo volcano and implications for volcanic hazard.

Science.gov (United States)

Pedrazzi, Dario; Aguirre Díaz, Gerardo; Sunyé Puchol, Ivan; Bartolini, Stefania; Geyer, Adelina

2016-04-01

The Trans-Mexican Volcanic Belt (TMVB) contains a large number of stratovolcanoes, some well-known, as Popocatepetl, Iztaccihuatl, Nevado de Toluca, or Colima and many others of more modest dimensions that are not well known but constitute the majority in the TMVB. Such volcanoes are, for example, Tequila, San Juan, Sangangüey, Cerro Culiacán, Cerro Grande, El Zamorano, La Joya, Palo Huerfano, Jocotitlán, Altamirano and Temascalcingo, among many others. The Temascalcingo volcano (TV) is an andesitic-dacitic stratovolcano located in the Trans-Mexican Volcanic Belt (TMVB) at the eastern part of the Acambay Graben (northwest portion of Estado de México). The TV is composed mainly by dacitic, porphyritic lavas, block and ash deposits and subordinate pumice fall deposits and ignimbrites (Roldán-Quintana et al., 2011). The volcanic structure includes a summit caldera that has a rectangular shape, 2.5×3.5 km, with the largest side oriented E-W, parallel to major normal faults affecting the edifice. The San Mateo Pumice eruption is one of the greatest paroxysmal episodes of this volcano with pumice deposits mainly exposed at the scarp of the Acambay-Tixmadeje fault and at the northern and northeastern flanks of TV. It overlies a paleosol dated at 25 Ka. A NE-trending dispersion was obtained from field data covering an area of at least 80 km2. These deposits overlie older lava flows and mud flows and are discontinuously covered and eroded by younger reworked deposits of Temascalcingo volcano. This event represents a highly explosive phase that generated a relatively thick and widespread pumice fallout deposit that may occur again in future eruptions. A similar eruption today would have a significantly impact in the region, overall due to the fact that there has been no systematic assessment of the volcanic hazard in any of the studies that have been conducted so far in the area. So, this is a pending and urgent subject that must be tackled without delay. Financed by

Exploring the atmospheric chemistry of O2SO3− and assessing the maximum turnover number of ion-catalysed H2SO4 formation

Directory of Open Access Journals (Sweden)

N. Bork

2013-04-01

Full Text Available It has recently been demonstrated that the O2SO3− ion forms in the atmosphere as a natural consequence of ionizing radiation. Here, we present a density functional theory-based study of the reactions of O2SO3− with O3. The most important reactions are (a oxidation to O2SO3− and (b cluster decomposition into SO3, O2 and O3−. The former reaction is highly exothermic, and the nascent O2SO3− will rapidly decompose into SO4− and O2. If the origin of O2SO3− is SO2 oxidation by O3−, the latter reaction closes a catalytic cycle wherein SO2 is oxidized to SO3. The relative rate between the two major sinks for O2SO3− is assessed, thereby providing a measure of the maximum turnover number of ion-catalysed SO2 oxidation, i.e. how many SO2 can be oxidized per free electron. The rate ratio between reactions (a and (b is significantly altered by the presence or absence of a single water molecule, but reaction (b is in general much more probable. Although we are unable to assess the overall importance of this cycle in the real atmosphere due to the unknown influence of CO2 and NOx, we roughly estimate that ion-induced catalysis may contribute with several percent of H2SO4 levels in typical CO2-free and low NOx reaction chambers, e.g. the CLOUD chamber at CERN.

CO2 diffuse emission from maar lake: An example in Changbai volcanic field, NE China

Science.gov (United States)

Sun, Yutao; Guo, Zhengfu; Liu, Jiaqi; Du, Jianguo

2018-01-01

Numerous maars and monogenetic volcanic cones are distributed in northeast China, which are related to westward deep subduction of the Pacific Ocean lithosphere, comprising a significant part of the "Pacific Ring of Fire". It is well known that diffuse CO2 emissions from monogenetic volcanoes, including wet (e.g., maar lake) and dry degassing systems (e.g., soil diffuse emission, fault degassing, etc.), may contribute to budget of globally nature-derived greenhouse gases. However, their relationship between wet (e.g., maar lake) and concomitant dry degassing systems (e.g., soil diffuse emission, fault degassing, etc.) related to monogenetic volcanic field is poorly understood. Yuanchi maar, one of the typical monogenetic volcanic systems, is located on the eastern flank of Tianchi caldera in Changbai volcanic field of northeast China, which displays all of three forms of CO2 degassing including the maar lake, soil micro-seepage and fault degassing. Measurements of efflux of CO2 diffusion from the Yuanchi maar system (YMS) indicate that the average values of CO2 emissions from soil micro-seepage, fault degassing and water-air interface diffusion are 24.3 ± 23.3 g m- 2 d- 1, 39.2 ± 22.4 g m- 2 d- 1 and 2.4 ± 1.1 g m- 2 d- 1, respectively. The minimum output of CO2 diffuse emission from the YMS to the atmosphere is about 176.1 ± 88.3 ton/yr, of which 80.4% results from the dry degassing system. Degassing from the fault contributes to the most of CO2 emissions in all of the three forms of degassing in the YMS. Contributions of mantle, crust, air and organic CO2 to the soil gas are 0.01-0.10%, 10-20%, 32-36% and 48-54%, respectively, which are quantitatively constrained by a He-C isotope coupling calculation model. We propose that CO2 exsolves from the upper mantle melting beneath the Tianchi caldera, which migrates to the crustal magma chamber and further transports to the surface of YMS along the deep fault system. During the transportation processes, the emission

Volcanic ash as fertiliser for the surface ocean

Directory of Open Access Journals (Sweden)

B. Langmann

2010-04-01

Full Text Available Iron is a key limiting micro-nutrient for marine primary productivity. It can be supplied to the ocean by atmospheric dust deposition. Volcanic ash deposition into the ocean represents another external and so far largely neglected source of iron. This study demonstrates strong evidence for natural fertilisation in the iron-limited oceanic area of the NE Pacific, induced by volcanic ash from the eruption of Kasatochi volcano in August 2008. Atmospheric and oceanic conditions were favourable to generate a massive phytoplankton bloom in the NE Pacific Ocean which for the first time strongly suggests a connection between oceanic iron-fertilisation and volcanic ash supply.

Results of aerosol and SO/sub 2/ measurements at Neurath fossil-fuel power plant in November 1974

Energy Technology Data Exchange (ETDEWEB)

Paffrath, D; Peters, W

1975-11-01

The structure of cooling tower plumes depends on meteorological conditions, especially on wind, temperature gradients, and turbulence. This influence of meteorological atmospheric conditions on the plumes may be quantitatively described by so-called diffusion parameters. These parameters may be determined with the aid of tracer measurements by determining tracer diffusion and, from the distribution of the tracers, calculating the diffusion parameters. At the Neurath power plant, there were three of these tracers. First, the vertical concentration distribution of the atmospheric background aerosol may yield information on the vertical stratification. Secondly, pollutants from anthropogenic sources, e.g., from the stacks of Neurath fossil-fuel power plant itself, may be used for investigation. In the present study, particle concentrations and SO/sub 2/ content of the air due to the waste gases from the power plant stacks were used for measurement.

Radioactivity level and soil radon measurement of a volcanic area in Cameroon

International Nuclear Information System (INIS)

Ngachin, M.; Garavaglia, M.; Giovani, C.; Kwato Njock, M.G.; Nourreddine, A.

2008-01-01

The radioactivity level of soils in a volcanic area in Cameroon was determined and discussed. Thirty soils samples were collected from Buea and Limbe cities located in the south-western Cameroon. These two regions are known for theirs volcanic grounds due to the presence of Mount Cameroon Mountain. The activity concentrations of natural radionuclides as well as that of the fission product were evaluated by gamma-ray spectrometry using a hyper-purity germanium detector (HPGe). The ranges of concentrations in the surveyed soils were 11-17 Bq kg -1 , 22-36 Bq kg -1 and 43-201 Bq kg -1 for 226 Ra, 232 Th and 40 K, respectively. The radioisotope 137 Cs was also found but in a very small amount. The outdoor absorbed dose rate 1 m above ground with the corresponding annual effective dose rate, assuming a 20% occupancy factor was estimated. The radium equivalent and the external hazard index were also evaluated and results are compared with available data from other studies and with the world average value [United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR), 1988. Sources, Effects and Risks of Ionizing Radiation. Report to the General Assembly on the Effects of Atomic Radiation. United Nations, New York; UNSCEAR, 2000. Sources and Effects of Ionizing Radiations. Report to the General Assembly with Scientific Annexes. United Nations, New York]. A solid state nuclear track detector (SSNTD), LR-115 was used for soil radon measurements at a depth of 50 cm. The ranges of soil radon concentrations were 6.7-10.8 kBq m -3 and 5.5-8.7 kBq m -3 in Buea and Limbe, respectively. A positive correlation was found between concentrations of radium measured with γ-spectrometry and the soil radon concentrations measured with the nitrate cellulose detectors. The results of this study provide the radioactivity level in soil of a volcanic area, which has been found to be within the safety limits. The south-western Cameroon can be considered as having normal

Geotourism and volcanoes: health hazards facing tourists at volcanic and geothermal destinations.

Science.gov (United States)

Heggie, Travis W

2009-09-01

Volcano tourism and tourism to geothermal destinations is increasingly popular. If such endeavors are to be a sustainable sector of the tourism industry, tourists must be made aware of the potential health hazards facing them in volcanic environments. With the aim of creating awareness amongst the tourism industry and practitioners of travel medicine, this paper reviews the potential influences and effects of volcanic gases such as carbon dioxide (CO(2)), hydrogen sulfide (H(2)S), sulfur dioxide (SO(2)), and hydrogen chloride/hydrochloric acid (HCl). It also reviews the negative health impacts of tephra and ash, lava flows, landslides, and mudflows. Finally, future research striving to quantify the health risks facing volcano tourists is recommended.

Environmental radioactivity level and soil radon measurement of a volcanic region in Cameroon

International Nuclear Information System (INIS)

Ngachin, M.; Garavaglia, M.; Giovani, C.; Kwato Njock, M.G.

2007-02-01

A part of the survey programme on the evaluation of environmental radioactivity in Cameroon has just been initiated. The radioactivity level of soils in a volcanic area in Cameroon was determined and discussed. 30 soils samples were collected from Buea and Limbe cities located in the south-western Cameroon. These two regions are known for theirs volcanic grounds due to the presence of Mount Cameroon mountain. The activity concentrations of natural radionuclides as well as that of the fission product were evaluated by gamma-ray spectrometry using a hyper purity germanium detector (HPGe). The ranges of concentrations in the surveyed soils were 11 - 17 Bq kg -1 , 22 - 36 Bq kg -1 and 43 - 201 Bq kg -1 for 226 Ra, 232 Th and 40 K, respectively. The radioisotope 137 Cs was also found but in a very small amount. The outdoor absorbed dose rate 1 m above ground with the corresponding annual effective dose rate, assuming a 20% occupancy factor were estimated. The radium equivalent and the external hazard index were also evaluated and results are compared with available data from other studies and with the world average value (UNSCEAR, 1988, 2000). A solid state nuclear track detector (SSNTDs), LR-115 was used for soil radon measurements at a depth of 50 cm. The ranges of soil radon concentrations were 6.7 - 10.8 kBq m -3 and 5.5 - 8.7 kBq m -3 in Buea and Limbe, respectively. A positive correlation was found between concentrations of radium measured with γ-spectrometry and the soil radon concentrations measured with the nitrate cellulose detectors. The results of this study provide the radioactivity level in soil of a volcanic area, which has been found to be within the safety limits. The south-western Cameroon can be considered as having normal natural background radiation in normal living conditions. (author)

Continuous measurements of radon content in groundwater on the volcanic site of ''Piton de la Fournaise'' (Island of Reunion, France)

International Nuclear Information System (INIS)

Barillon, R.; University of Exeter; Violette, S.; Carbonnel, J.P.; Nicolini, E.; Klein, D.; Chambaudet, A.; Heath, M.J.; Merefield, J.

1993-01-01

In the framework of the ''R.E.M.M.I.'' programme (French programme to study the ship relation between water and magma in intertropical environment), different physical and chemical parameters (radon level, conductivity, pH, CO2 level, helium level, temperature) are monitored in the drainage waters of the ''Tunnel de la Riviere de l'Est'' in order to correlate their variations with the stress in the volcanic chain of the ''Piton de la Fournaise''. In a first period of experimentation, during the dry season, the radon concentrations in water have been measured by nuclear track detectors (LR115). In a second field session, during the wet season, a complementary technique has been added: a continuous measurement with a portable proportional counter. The radon measurements and the other results suggest potential for continuous monitoring, through various steps of the annual cycle likely to be indicators of volcanic activity. This second phase should begin in 1992, September in a new European Programme. (author)

SO3 formation from the X-ray photolysis of SO2 astrophysical ice analogues: FTIR spectroscopy and thermodynamic investigations.

Science.gov (United States)

de Souza Bonfim, Víctor; Barbosa de Castilho, Roberto; Baptista, Leonardo; Pilling, Sergio

2017-10-11

In this combined experimental-theoretical work we focus on the physical and chemical changes induced by soft X-rays on sulfur dioxide (SO 2 ) ice at a very low temperature, in an attempt to clarify and quantify its survival and chemical changes in some astrophysical environments. SO 2 is an important constituent of some Jupiter moons and has also been observed in ices around protostars. The measurements were performed at the Brazilian Synchrotron Light Source (LNLS/CNPEM), in Campinas, Brazil. The SO 2 ice sample (12 K) was exposed to a broadband beam of mainly soft X-rays (6-2000 eV) and in situ analyses were performed by IR spectroscopy. The X-ray photodesorption yield (upper limit) was around 0.25 molecules per photon. The values determined for the effective destruction (SO 2 ) and formation (SO 3 ) cross sections were 2.5 × 10 -18 cm 2 and 2.1 × 10 -18 cm 2 , respectively. The chemical equilibrium (88% of SO 2 and 12% of SO 3 ) was reached after the fluence of 1.6 × 10 18 photons cm -2 . The SO 3 formation channels were studied at the second-order Møller-Plesset perturbation theory (MP2) level, which showed the three most favorable reaction routes (ΔH < -79 kcal mol -1 ) in simulated SO 2 ice: (i) SO + O 2 → SO 3 , (ii) SO 2 + O → SO 3 , and (iii) SO 2 + O + → SO 3 + + e - → SO 3 . The amorphous solid environment effect decreases the reactivity of intermediate species towards SO 3 formation, and ionic species are even more affected. The experimentally determined effective cross sections and theoretical reaction channels identified in this work allow us to better understand the chemical evolution of certain sulfur-rich astrophysical environments.

Calculation of phase equilibria in the Na2SO4-K2SO4-Cs2SO4-H2O system at 25 deg C

International Nuclear Information System (INIS)

Filippov, V.K.; Kalinkin, A.M.; Vasin, S.K.

1990-01-01

Calculation results of solubility diagram and water activity in saturated solutions of Na 2 SO 4 -K 2 SO 4 -Cs 2 SO 4 -H 2 O system at 25 deg C are presented. It is shown that for the calculation of quaternary systems one can use the Pitzer equations. Solubility diagram for the system studied is plotted and data on composition and water activity of solutions saturated by two or three solid phases are given. Classification of nonvariant equilibria from the viewpoint of isomorphism of solubility and fusibility diagrams permits to depict the direction of phase processes during isothermal evaporation of water

Monitoring diffuse degassing in monogenetic volcanic field during seismic-volcanic unrest: the case of Tenerife North-West Rift Zone (NWRZ), Canary Islands, Spain

Science.gov (United States)

García, E.; Botelho, A. H.; Regnier, G. S. G.; Rodríguez, F.; Alonso Cótchico, M.; Melián, G.; Asensio-Ramos, M.; Padrón, E.; Hernández, P. A.; Pérez, N. M.

2017-12-01

Tenerife North-West Rift-Zone (NWRZ) is the most active volcano of the oceanic active volcanic island of Tenerife and the scenario of three historical eruptions (Boca Cangrejo S. XVI, Arenas Negras 1706 and Chinyero 1909). Since no visible degassing (fumaroles, etc.) at Tenerife NWRZ occurs, a geochemical monitoring program at Tenerife NWRZ was established mainly consisting on performing soil CO2 efflux surveys (50 surveys since 2000) to evaluate the temporal and spatial variations of soil CO2 efflux measurements and the diffuse CO2 emission rate. To do so, about 340 sampling sites were selected for each survey to obtain a homogeneous distribution after taking into consideration the local geology, structure, and accessibility. Measurements of soil CO2 efflux were performed in situ by means of a portable non-dispersive infrared sensor following the accumulation chamber method. The soil CO2 efflux values of the 2017 survey ranged from non-detectable to 46.6 g m-2 d-1. Statistical-graphical analysis of the 2017 data show two different geochemical populations; background (B) and peak (P) represented by 93.3% and 1.9% of the total data, respectively. The geometric means of the B and P populations are 2.4 and 19.1 g m-2 d-1, respectively. Most of the area showed B values while the P values were mainly observed at the N-W side of the volcanic rift. To estimate the diffuse CO2 emission in metric tons per day released from Tenerife NWRZ (75 km2) for the 2017 survey, we ran about 100 sGs simulations. The estimated 2017 diffuse CO2 output released to atmosphere by the Tenerife NWRZ volcano was 297 ± 13 t d-1. This 2017 diffuse CO2 emission rate value is relatively higher than the estimated background value (144 t d-1) and falls within the estimated background range (72 - 321 t d-1) observed for Tenerife NWRZ volcano during the 2000-2017 period. The observed temporal variation in the diffuse CO2 degassing output during this period does not seem to be driven by external

Sulfur Chemistry in the Envelope of VY Canis Majoris: Detailed Analysis of SO and SO2 Emission

Science.gov (United States)

Adande, G. R.; Edwards, J. L.; Ziurys, L. M.

2013-11-01

Detailed radiative transfer modeling has been carried out for SO2 and SO originating in the envelope of the O-rich supergiant star VY Canis Majoris (VY CMa). A total of 27 transitions of SO2 and 7 transitions of SO lying in the energy range 3.0-138.2 cm-1 were analyzed using a new non-LTE radiative transfer code that incorporates non-spherical geometries. The spectra were primarily obtained from the Arizona Radio Observatory (ARO) 1 mm spectral survey of VY CMa, conducted with the Submillimeter Telescope; additional lines were measured with the ARO 12 m antenna at 2 and 3 mm. SO2 and SO were found to arise from five distinct outflows within the envelope, four which are asymmetric with respect to the star. Three flows arise from high-velocity red-shifted material, one from a blue-shifted wind, and the final from a classic "spherical" expansion. In the spherical component, the peak fractional abundance, relative to H2, of both molecules is f ~ 2.5 × 10-7 at r ~ 25 R *, and steadily decreases outward. SO2 appears to be a "parent" molecule, formed near the stellar photosphere. In the asymmetric outflows, both SO and SO2 are more prominent at large stellar radii in dense (106-107 cm-3), clumpy material, achieving their maximum abundance between 200 and 600 R * with f ~ 3.0 × 10-8-1.5 × 10-7. These results suggest that in the collimated outflows, both species are either produced by shock chemistry or are remnant inner shell material swept up in the high-velocity winds.

Lidar detection of carbon dioxide in volcanic plumes

Science.gov (United States)

Fiorani, Luca; Santoro, Simone; Parracino, Stefano; Maio, Giovanni; Del Franco, Mario; Aiuppa, Alessandro

2015-06-01

Volcanic gases give information on magmatic processes. In particular, anomalous releases of carbon dioxide precede volcanic eruptions. Up to now, this gas has been measured in volcanic plumes with conventional measurements that imply the severe risks of local sampling and can last many hours. For these reasons and for the great advantages of laser sensing, the thorough development of volcanic lidar has been undertaken at the Diagnostics and Metrology Laboratory (UTAPRAD-DIM) of the Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA). In fact, lidar profiling allows one to scan remotely volcanic plumes in a fast and continuous way, and with high spatial and temporal resolution. Two differential absorption lidar instruments will be presented in this paper: BILLI (BrIdge voLcanic LIdar), based on injection seeded Nd:YAG laser, double grating dye laser, difference frequency mixing (DFM) and optical parametric amplifier (OPA), and VULLI (VULcamed Lidar), based on injection seeded Nd:YAG laser and optical parametric oscillator (OPO). The first one is funded by the ERC (European Research Council) project BRIDGE and the second one by the ERDF (European Regional Development Fund) project VULCAMED. While VULLI has not yet been tested in a volcanic site, BILLI scanned the gas emitted by Pozzuoli Solfatara (Campi Flegrei volcanic area, Naples, Italy) during a field campaign carried out from 13 to 17 October 2014. Carbon dioxide concentration maps were retrieved remotely in few minutes in the crater area. Lidar measurements were in good agreement with well-established techniques, based on different operating principles. To our knowledge, it is the first time that carbon dioxide in a volcanic plume is retrieved by lidar, representing the first direct measurement of this kind ever performed on an active volcano and showing the high potential of laser remote sensing in geophysical research.

Isopiestic Investigation of the Osmotic and Activity Coefficients of {yMgCl2 + (1 - y)MgSO4}(aq) and the Osmotic Coefficients of Na2SO4.MgSO4(aq) at 298.15 K

Energy Technology Data Exchange (ETDEWEB)

Miladinovic, J; Ninkovic, R; Todorovic, M; Rard, J A

2007-06-06

Isopiestic vapor pressure measurements were made for {l_brace}yMgCl{sub 2} + (1-y)MgSO{sub 4}{r_brace}(aq) solutions with MgCl{sub 2} ionic strength fractions of y = 0, 0.1997, 0.3989, 0.5992, 0.8008, and (1) at the temperature 298.15 K, using KCl(aq) as the reference standard. These measurements for the mixtures cover the ionic strength range I = 0.9794 to 9.4318 mol {center_dot} kg{sup -1}. In addition, isopiestic measurements were made with NaCl(aq) as reference standard for mixtures of {l_brace}xNa{sub 2}SO{sub 4} + (1-x)MgSO{sub 4}{r_brace}(aq) with the molality fraction x = 0.50000 that correspond to solutions of the evaporite mineral bloedite (astrakanite), Na{sub 2}Mg(SO{sub 4}){sub 2} {center_dot} 4H{sub 2}O(cr). The total molalities, m{sub T} = m(Na{sub 2}SO{sub 4}) + m(MgSO{sub 4}), range from m{sub T} = 1.4479 to 4.4312 mol {center_dot} kg{sup -1} (I = 5.0677 to 15.509 mol {center_dot} kg{sup -1}), where the uppermost concentration is the highest oversaturation molality that could be achieved by isothermal evaporation of the solvent at 298.15 K. The parameters of an extended ion-interaction (Pitzer) model for MgCl2(aq) at 298.15 K, which were required for an analysis of the {l_brace}yMgCl{sub 2} + (1-y)MgSO{sub 4}{r_brace}(aq) mixture results, were evaluated up to I = 12.025 mol {center_dot} kg{sup -1} from published isopiestic data together with the six new osmotic coefficients obtained in this study. Osmotic coefficients of {l_brace}yMgCl{sub 2} + (1-y)MgSO{sub 4}{r_brace}(aq) solutions from the present study, along with critically-assessed values from previous studies, were used to evaluate the mixing parameters of the extended ion-interaction model.

European intercomparison workshops on air quality monitoring. Vol. 4. Measuring NO, NO{sub 2}, O{sub 3} and SO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Muecke, H.G.; Kollar, M. [Umweltbundesamt, Berlin (Germany). WHO-Zentrum zur Ueberwachung der Luftguete und Bekaempfung der Luftverschmutzung; Kratz, M.; Medem, A.; Rudolf, W.; Stummer, V.; Sukale, G. [Umweltbundesamt, Langen (Germany). UBA Pilotstation

2000-07-01

This report presents the results of two European Intercomparison Workshops on Air Quality Monitoring (NO, NO{sub 2}, O{sub 3}, and SO{sub 2}). The Workshops were a contribution to continuing quality assurance and quality control activities on air quality monitoring for Member States of the WHO European Region. Fourteen institutes mainly from Central and Eastern Europe used the opportunity to compare their measurement methods (15 manual methods and 24 monitors) and standards. (orig.)

Study on the Effect of Straw Fiber on the Performance of Volcanic Slag Concrete

Science.gov (United States)

Xiao, Li-guang; Liu, Xi-xu

2018-03-01

In this paper, the effects of straw fiber on the working performance, mechanical properties and frost resistance of volcanic slag lightweight aggregate concrete were studied. The experimental results show that the straw fiber is subjected to surface carbonization treatment and mixed into the volcanic slag light aggregate concrete. The flexural strength and fracture pressure ratio of volcanic slag lightweight aggregate concrete are improved obviously Improved volcanic slag lightweight aggregate concrete brittleness improves toughness. Carbonized straw fiber greatly improves the frost resistance of volcanic slag lightweight aggregate concrete. So that the volcanic slag light aggregate concrete freeze-thaw cycle can reach 300 times.

Volcanic signals in oceans

KAUST Repository

Stenchikov, Georgiy L.; Delworth, Thomas L.; Ramaswamy, V.; Stouffer, Ronald J.; Wittenberg, Andrew; Zeng, Fanrong

2009-01-01

Sulfate aerosols resulting from strong volcanic explosions last for 2–3 years in the lower stratosphere. Therefore it was traditionally believed that volcanic impacts produce mainly short-term, transient climate perturbations. However, the ocean

The volcanic rocks construction of the late paleozoic era and uranium mineralization in Beishan area of Gansu province

International Nuclear Information System (INIS)

An Zhengchang; Luo Xiaoqiang

2010-01-01

Late Paleozoic volcanic rocks in Beishan area are the favorable constructions of hydrothermal type and volcanic type deposit. From the distribution of volcanic rocks, the volcanic compositions, the volcanic facies, volcanic eruption method and rhythm, chemical and trace elements compositions, and so on, it discusses the characteristics of the Late Devonian volcanic construction in this area and its relationship with uranium mineralization, analyzes the role of volcanic ore-control mechanism, and summarizes uranium ore forming regularity of volcanic construction in Late Paleozoic. (authors)

Volcanism and associated hazards: the Andean perspective

Science.gov (United States)

Tilling, R. I.

2009-12-01

Andean volcanism occurs within the Andean Volcanic Arc (AVA), which is the product of subduction of the Nazca Plate and Antarctica Plates beneath the South America Plate. The AVA is Earth's longest but discontinuous continental-margin volcanic arc, which consists of four distinct segments: Northern Volcanic Zone, Central Volcanic Zone, Southern Volcanic Zone, and Austral Volcanic Zone. These segments are separated by volcanically inactive gaps that are inferred to indicate regions where the dips of the subducting plates are too shallow to favor the magma generation needed to sustain volcanism. The Andes host more volcanoes that have been active during the Holocene (past 10 000 years) than any other volcanic region in the world, as well as giant caldera systems that have produced 6 of the 47 largest explosive eruptions (so-called "super eruptions") recognized worldwide that have occurred from the Ordovician to the Pleistocene. The Andean region's most powerful historical explosive eruption occurred in 1600 at Huaynaputina Volcano (Peru). The impacts of this event, whose eruptive volume exceeded 11 km3, were widespread, with distal ashfall reported at distances >1000 km away. Despite the huge size of the Huaynaputina eruption, human fatalities from hazardous processes (pyroclastic flows, ashfalls, volcanogenic earthquakes, and lahars) were comparatively small owing to the low population density at the time. In contrast, lahars generated by a much smaller eruption (Colombia) killed about 25 000 people - the worst volcanic disaster in the Andean region as well as the second worst in the world in the 20th century. The Ruiz tragedy has been attributed largely to ineffective communications of hazards information and indecisiveness by government officials, rather than any major deficiencies in scientific data. Ruiz's disastrous outcome, however, together with responses to subsequent hazardous eruptions in Chile, Colombia, Ecuador, and Peru has spurred significant

Uptake of SO/sub 2/ and NO/sub 2/ by the isolated upper airways

Energy Technology Data Exchange (ETDEWEB)

Yokoyama, E

1968-01-01

SO/sub 2/ and NO/sub 2/ concentrations were measured above and below isolated tracheas of 2 dogs and 3 rabbits. Air--gas mixtures were pumped through nose to upper trachea for 10 to 15 min at rates of 3.5 and 0.75 liters/min, respectively. Gas concentrations ranged from 7 to 87 ppM SO/sub 2/ and from 4 to 41 ppM NO/sub 2/. The rate of uptake for the isolated airways was a generally constant 93.7% for SO/sub 2/ and 42.1% for NO/sub 2/, a significant difference.

SO2 frost - UV-visible reflectivity and Io surface coverage

Science.gov (United States)

Nash, D. B.; Fanale, F. P.; Nelson, R. M.

1980-01-01

The reflectance spectrum in the range 0.24-0.85 microns of SO2 frost is measured in light of the discovery of SO2 gas in the atmosphere of Io and the possible discovery of the frost on its surface. Frost deposits up to 1.5 mm thick were grown in vacuum at 130 K and bi-directional reflectance spectra were obtained. Typical SO2 frost is found to exhibit very low reflectivity (2-5%) at 0.30 microns, rising steeply at 0.32 microns to attain a maximum reflectivity (75-80%) at 4.0 microns and uniformly high reflectivity throughout the visible and near infrared. Comparison with the full disk spectrum of Io reveals that no more than 20% of the surface can be covered with optically thick SO2 frost. Combinations of surface materials including SO2 frost which can produce the observed spectrum are indicated.

Rapid uplift in Laguna del Maule volcanic field of the Andean Southern Volcanic Zone (Chile) measured by satellite radar interferometry

Science.gov (United States)

Feigl, K.; Ali, T.; Singer, B. S.; Pesicek, J. D.; Thurber, C. H.; Jicha, B. R.; Lara, L. E.; Hildreth, E. W.; Fierstein, J.; Williams-Jones, G.; Unsworth, M. J.; Keranen, K. M.

2011-12-01

The Laguna del Maule (LdM) volcanic field of the Andean Southern Volcanic Zone extends over 500 square kilometers and comprises more than 130 individual vents. As described by Hildreth et al. (2010), the history has been defined from sixty-eight Ar/Ar and K-Ar dates. Silicic eruptions have occurred throughout the past 3.7 Ma, including welded ignimbrite associated with caldera formation at 950 ka, small rhyolitic eruptions between 336 and 38 ka, and a culminating ring of 36 post-glacial rhyodacite and rhyolite coulees and domes that encircle the lake. Dating of five post-glacial flows implies that these silicic eruptions occurred within the last 25 kyr. Field relations indicate that initial eruptions comprised modest volumes of mafic rhyodacite magma that were followed by larger volumes of high silica rhyolite. The post-glacial flare-up of silicic magmatism from vents distributed around the lake, is unprecedented in the history of this volcanic field. Using satellite radar interferometry (InSAR), Fournier et al. (2010) measured uplift at a rate of more than 180 mm/year between 2007 and 2008 in a round pattern centered on the west side of LdM. More recent InSAR observations suggest that rapid uplift has continued from 2008 through early 2011. In contrast, Fournier et al. found no measurable deformation in an interferogram spanning 2003 through 2004. In this study, we model the deformation field using the General Inversion of Phase Technique (GIPhT), as described by Feigl and Thurber (2009). Two different models fit the data. The first model assumes a sill at ~5 km depth has been inflating at a rate of more than 20 million cubic meters per year since 2007. The second model assumes that the water level in the lake dropped at a rate of 20 m/yr from January 2007 through February 2010, thus reducing the load on an elastic simulation of the crust. The rate of intrusion inferred from InSAR is an order of magnitude higher than the average rate derived from well-dated arc

Characteristics of volcanic reservoirs and distribution rules of effective reservoirs in the Changling fault depression, Songliao Basin

Directory of Open Access Journals (Sweden)

Pujun Wang

2015-11-01

Full Text Available In the Songliao Basin, volcanic oil and gas reservoirs are important exploration domains. Based on drilling, logging, and 3D seismic (1495 km2 data, 546 sets of measured physical properties and gas testing productivity of 66 wells in the Changling fault depression, Songliao Basin, eruptive cycles and sub-lithofacies were distinguished after lithologic correction of the 19,384 m volcanic well intervals, so that a quantitative analysis was conducted on the relation between the eruptive cycles, lithologies and lithofacies and the distribution of effective reservoirs. After the relationship was established between lithologies, lithofacies & cycles and reservoir physical properties & oil and gas bearing situations, an analysis was conducted on the characteristics of volcanic reservoirs and the distribution rules of effective reservoirs. It is indicated that 10 eruptive cycles of 3 sections are totally developed in this area, and the effective reservoirs are mainly distributed at the top cycles of eruptive sequences, with those of the 1st and 3rd Members of Yingcheng Formation presenting the best reservoir properties. In this area, there are mainly 11 types of volcanic rocks, among which rhyolite, rhyolitic tuff, rhyolitic tuffo lava and rhyolitic volcanic breccia are the dominant lithologies of effective reservoirs. In the target area are mainly developed 4 volcanic lithofacies (11 sub-lithofacies, among which upper sub-lithofacies of effusive facies and thermal clastic sub-lithofacies of explosion lithofacies are predominant in effective reservoirs. There is an obvious corresponding relationship between the physical properties of volcanic reservoirs and the development degree of effective reservoirs. The distribution of effective reservoirs is controlled by reservoir physical properties, and the formation of effective reservoirs is influenced more by porosity than by permeability. It is concluded that deep volcanic gas exploration presents a good

Sulfur chemistry in the envelope of VY Canis Majoris: Detailed analysis of SO and SO2 emission

International Nuclear Information System (INIS)

Adande, G. R.; Edwards, J. L.; Ziurys, L. M.

2013-01-01

Detailed radiative transfer modeling has been carried out for SO 2 and SO originating in the envelope of the O-rich supergiant star VY Canis Majoris (VY CMa). A total of 27 transitions of SO 2 and 7 transitions of SO lying in the energy range 3.0-138.2 cm –1 were analyzed using a new non-LTE radiative transfer code that incorporates non-spherical geometries. The spectra were primarily obtained from the Arizona Radio Observatory (ARO) 1 mm spectral survey of VY CMa, conducted with the Submillimeter Telescope; additional lines were measured with the ARO 12 m antenna at 2 and 3 mm. SO 2 and SO were found to arise from five distinct outflows within the envelope, four which are asymmetric with respect to the star. Three flows arise from high-velocity red-shifted material, one from a blue-shifted wind, and the final from a classic 'spherical' expansion. In the spherical component, the peak fractional abundance, relative to H 2 , of both molecules is f ∼ 2.5 × 10 –7 at r ∼ 25 R * , and steadily decreases outward. SO 2 appears to be a 'parent' molecule, formed near the stellar photosphere. In the asymmetric outflows, both SO and SO 2 are more prominent at large stellar radii in dense (10 6 -10 7 cm –3 ), clumpy material, achieving their maximum abundance between 200 and 600 R * with f ∼ 3.0 × 10 –8 -1.5 × 10 –7 . These results suggest that in the collimated outflows, both species are either produced by shock chemistry or are remnant inner shell material swept up in the high-velocity winds.

Thermal Measurement during Electrolysis of Pd-Ni Thin-film -Cathodes in Li2SO4/H2O Solution

Science.gov (United States)

Castano, C. H.; Lipson, A. G.; S-O, Kim; Miley, G. H.

2002-03-01

Using LENR - open type calorimeters, measurements of excess heat production were carried out during electrolysis in Li_2SO_4/H_2O solution with a Pt-anode and Pd-Ni thin film cathodes (2000-8000 Åthick) sputtered on the different dielectric substrates. In order to accurately evaluate actual performance during electrolysis runs in the open-type calorimeter used, considering effects of heat convection, bubbling and possible H_2+O2 recombination, smooth Pt sheets were used as cathodes. Pt provides a reference since it does not produce excess heat in the light water electrolyte. To increase the accuracy of measurements the water dissociation potential was determined for each cathode taking into account its individual over-voltage value. It is found that this design for the Pd-Ni cathodes resulted in the excess heat production of ~ 20-25 % of input power, equivalent to ~300 mW. In cases of the Pd/Ni- film fracture (or detachment from substrate) no excess heat was detected, providing an added reference point. These experiments plus use of optimized films will be presented.

Unzen volcanic rocks as heat source of geothermal activity

Energy Technology Data Exchange (ETDEWEB)

Hayashi, Masao; Sugiyama, Hiromi

1987-03-25

Only a few radiometric ages have been reported so far for the Unzen volcanic rocks. In this connection, in order to clarify the relation between volcanism and geothermal activity, fission track ages of zircon seperated from the Unzen volcanic rocks in western Kyushu have been dated. Since all the rocks are thought to be young, the external surface re-etch method was adopted. The results are that the age and standard error of the basal volcaniclastic rocks of the Tatsuishi formation are 0.28 +- 0.05 Ma and 0.25 +- 0.05 Ma. The next oldest Takadake lavas range from 0.26 to 0.20 Ma. The Kusenbudake lavas fall in a narrow range from 0.19 to 0.17 Ma. The latest Fugendake lavas are younger than 0.07 Ma.In conclusion, the most promising site for geothermal power generation is the Unzen hot spring field because of its very high temperature. After that, comes the Obama hot spring field because of the considerable high temperature chemically estimated. In addition, the northwestern area of the Unzen volcanic region will be promising for electric power generation in spite of no geothermal manifestations, since its volcanos are younger than 0.2 Ma. (14 figs, 14 tabs, 22 refs)

Microphysical Properties of Alaskan Volcanic Ash

Science.gov (United States)

Puthukkudy, A.; Espinosa, R.; Rocha Lima, A.; Remer, L.; Colarco, P. R.; Whelley, P.; Krotkov, N. A.; Young, K.; Dubovik, O.; Wallace, K.; Martins, J. V.

2017-12-01

Volcanic ash has the potential to cause a variety of severe problems for human health and the environment. Therefore, effective monitoring of the dispersion and fallout from volcanic ash clouds and characterization of the aerosol particle properties are essential. One way to acquire information from volcanic clouds is through satellite remote sensing: such images have greater coverage than ground-based observations and can present a "big picture" perspective. A challenge of remote sensing is that assumptions of certain properties of the target are often a pre-requisite for making accurate and quantitative retrievals. For example, detailed information about size distribution, sphericity, and optical properties of the constituent matter is needed or must be assumed. The same kind of information is also needed for atmospheric transport models to properly simulate the dispersion and fallout of volcanic ash. Presented here is a laboratory method to determine the microphysical and optical properties of volcanic ash samples collected from two Alaskan volcanoes with markedly different compositions. Our method uses a Polarized Imaging Nephelometer (PI-Neph) and a system that re-suspends the particles in an air flow. The PI-Neph measures angular light scattering and polarization of the re-suspended particles from 3o to 175o in scattering angle, with an angular resolution of 1o . Primary measurements include phase function and polarized phase function at three wavelengths (445nm, 532nm, and 661nm). Size distribution, sphericity, and complex refractive index are retrieved indirectly from the PI-Neph measurements using the GRASP (Generalized Retrieval of Aerosol and Surface Properties) inversion algorithm. We report the results of this method applied to samples from the Mt. Okmok (2008) and Mt. Katmai (1912) volcanic eruptions. To our knowledge, this is the first time direct measurements of phase matrix elements of ash from Mt. Okmok and Mt. Katmai have been reported. Retrieved

Sodium intercalation in the phosphosulfate cathode NaFe2(PO4)(SO4)2

Science.gov (United States)

Ben Yahia, Hamdi; Essehli, Rachid; Amin, Ruhul; Boulahya, Khalid; Okumura, Toyoki; Belharouak, Ilias

2018-04-01

The compound NaFe2(PO4)(SO4)2 is successfully synthesized via a solid state reaction route and its crystal structure is determined using powder X-ray diffraction data. NaFe2(PO4)(SO4)2 phase is also characterized by cyclic voltammetry, galvanostatic cycling and electrochemical impedance spectroscopy. NaFe2(PO4)(SO4)2 crystallizes with the well-known NASICON-type structure. SAED and HRTEM experiments confirm the structural model, and no ordering between the PO4-3 and SO4-2 polyanions is detected. The electrochemical tests indicate that NaFe2(PO4)(SO4)2 is a 3 V sodium intercalating cathode. The electrical conductivity is relatively low (2.2 × 10-6 Scm-1 at 200 °C) and the obtained activation energy is ∼0.60eV. The GITT experiments indicate that the diffusivity values are in the range of 10-11-10-12 cm2/s within the measured sodium concentrations.

Volcanic deformation in the Andes

Science.gov (United States)

Riddick, S.; Fournier, T.; Pritchard, M.

2009-05-01

We present the results from an InSAR survey of volcanic activity in South America. We use data from the Japanese Space Agency's ALOS L-band radar satellite from 2006-2009. The L-band instrument provides better coherence in densely vegetated regions, compared to the shorter wave length C-band data. The survey reveals volcano related deformation in regions, north, central and southern, of the Andes volcanic arc. Since observations are limited to the austral summer, comprehensive coverage of all volcanoes is not possible. Yet, our combined observations reveal volcanic/hydrothermal deformation at Lonquimay, Llaima, Laguna del Maule, and Chaitén volcanoes, extend deformation measurements at Copahue, and illustrate temporal complexity to the previously described deformation at Cerro Hudson and Cordón Caulle. No precursory deformation is apparent before the large Chaitén eruption (VEI_5) of 2 May 2008, (at least before 16 April) suggesting rapid magma movement from depth at this long dormant volcano. Subsidence at Ticsani Volcano occurred coincident with an earthquake swarm in the same region.

Sulfation of Condensed Potassium Chloride by SO2

DEFF Research Database (Denmark)

Sengeløv, Louise With; Hansen, Troels Bruun; Bartolomé, Carmen

2013-01-01

The interaction between alkali chloride and sulfur oxides has important implications for deposition and corrosion in combustion of biomass. In the present study, the sulfation of particulate KCl (90–125 μm) by SO2 was studied in a fixed bed reactor in the temperature range 673–1023 K and with rea......The interaction between alkali chloride and sulfur oxides has important implications for deposition and corrosion in combustion of biomass. In the present study, the sulfation of particulate KCl (90–125 μm) by SO2 was studied in a fixed bed reactor in the temperature range 673–1023 K...... and with reactant concentrations of 500–3000 ppm SO2, 1–20% O2, and 4–15% H2O. The degree of sulfation was monitored by measuring the formation of HCl. Analysis of the solid residue confirmed that the reaction proceeds according to a shrinking core model and showed the formation of an eutectic at higher...... temperatures. On the basis of the experimental results, a rate expression for the sulfation reaction was derived. The model compared well with literature data for sulfation of KCl and NaCl, and the results indicate that it may be applied at even higher SO2 concentrations and temperatures than those...

40 CFR 97.288 - CAIR SO2 allowance allocations to CAIR SO2 opt-in units.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR SO2 allowance allocations to CAIR SO2 opt-in units. 97.288 Section 97.288 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) FEDERAL NOX BUDGET TRADING PROGRAM AND CAIR NOX AND SO2 TRADING PROGRAMS...

40 CFR 96.288 - CAIR SO2 allowance allocations to CAIR SO2 opt-in units.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 20 2010-07-01 2010-07-01 false CAIR SO2 allowance allocations to CAIR SO2 opt-in units. 96.288 Section 96.288 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) NOX BUDGET TRADING PROGRAM AND CAIR NOX AND SO2 TRADING PROGRAMS FOR...

Volcanic CO2 Emissions and Glacial Cycles: Coupled Oscillations

Science.gov (United States)

Burley, J. M.; Huybers, P. J.; Katz, R. F.

2016-12-01

Following the mid-Pleistocene transition, the dominant period of glacial cycles changed from 40 ka to 100 ka. It is broadly accepted that the 40 ka glacial cycles were driven by cyclical changes in obliquity. However, this forcing does not explain the 100 ka glacial cycles. Mechanisms proposed for 100 ka cycles include isostatic bed depression and proglacial lakes destabilising the Laurentide ice sheet, non-linear responses to orbital eccentricity, and Antarctic ice sheets influencing deep-ocean stratification. None of these are universally accepted. Here we investigate the hypothesis that variations in volcanic CO2 emissions can cause 100 ka glacial cycles. Any proposed mechanism for 100 ka glacial cycles must give the Earth's climate system a memory of 10^4 - 10^5years. This timescale is difficult to achieve for surface processes, however it is possible for the solid Earth. Recent work suggests volcanic CO2 emissions change in response to glacial cycles [1] and that there could be a 50 ka delay in that response [2]. Such a lagged response could drive glacial cycles from 40 ka cycles to an integer multiple of the forcing period. Under what conditions could the climate system admit such a response? To address this, we use a simplified climate model modified from Huybers and Tziperman [3]. Our version comprises three component models for energy balance, ice sheet growth and atmospheric CO2 concentration. The model is driven by insolation alone with other components varying according to a system of coupled, differential equations. The model is run for 500 ka to produce several glacial cycles and the resulting changes in global ice volume and atmospheric CO2 concentration.We obtain a switch from 40 ka to 100 ka cycles as the volcanic CO2 response to glacial cycles is increased. These 100 ka cycles are phase-locked to obliquity, lasting 80 or 120 ka. Whilst the MOR response required (in this model) is larger than plausible estimates based on [2], it illustrates the

SO/sub 2/ injury to forests

Energy Technology Data Exchange (ETDEWEB)

Hontvedt, R

1970-01-01

Sulfur dioxide is one of the most important of the air pollutants which has produced damage to trees and other vegetation. This article gives some examples of SO/sub 2/ damage to forests: At Rjukan in Norway, at Naerkes-Kvarntorp in Sweden and in German industrial regions. Then a brief summary is given of the factors which determine the effects of SO/sub 2/ on plants. Significant differences in SO/sub 2/ resistance exist, both between species and between individuals of the same species. Deciduous trees are more resistant than conifers. There appears to be a positive correlation between CO/sub 2/ assimilation and SO/sub 2/ damage in some individuals. Factors which influence co2 assimilation include, for example, the leaf development state and environmental factors (light, water, temperature, etc.). High SO/sub 2/ concentrations in the air over a brief time period are distinctly more injurious than low concentrations over a long time. Fertilization may increase the resistance of forest trees to SO/sub 2/. Some insect types predispose to SO/sub 2/, partly by increasing the number of dead and weakened trees and partially by increasing parasitization by insects.