149 results on '"Carn, S."'
Search Results
2. VolKilau : Volcano Rapid Response Balloon Campaign during the 2018 Kilauea Eruption
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Vernier, J.-P., Kalnajs, L., Diaz, J. A., Reese, T., Corrales, E., Alan, A., Vernier, H., Holland, L., Patel, A., Rastogi, N., Wienhold, F., Carn, S., Krotkov, N., and Murray, J.
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- 2020
3. Underestimated Passive Volcanic Sulfur Degassing Implies Overestimated Anthropogenic Aerosol Forcing
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Jongebloed, U. A., primary, Schauer, A. J., additional, Cole‐Dai, J., additional, Larrick, C. G., additional, Wood, R., additional, Fischer, T. P., additional, Carn, S. A., additional, Salimi, S., additional, Edouard, S. R., additional, Zhai, S., additional, Geng, L., additional, and Alexander, B., additional
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- 2023
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4. Out of the blue: Volcanic SO2 emissions during the 2021–2022 eruptions of Hunga Tonga—Hunga Ha’apai (Tonga)
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Carn, S. A., Krotkov, N. A., Fisher, B. L., and Li, C.
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General Earth and Planetary Sciences - Abstract
Most volcanism on Earth is submarine, but volcanic gas emissions by submarine eruptions are rarely observed and hence largely unquantified. On 15 January 2022 a submarine eruption of Hunga Tonga-Hunga Ha’apai (HTHH) volcano (Tonga) generated an explosion of historic magnitude, and was preceded by ∼1 month of Surtseyan eruptive activity and two precursory explosive eruptions. We present an analysis of ultraviolet (UV) satellite measurements of volcanic sulfur dioxide (SO2) between December 2021 and the climactic 15 January 2022 eruption, comprising an unprecedented record of Surtseyan eruptive emissions. UV measurements from the Ozone Monitoring Instrument (OMI) on NASA’s Aura satellite, the Ozone Mapping and Profiler Suite (OMPS) on Suomi-NPP, the Tropospheric Monitoring Instrument (TROPOMI) on ESA’s Sentinel-5P, and the Earth Polychromatic Imaging Camera (EPIC) aboard the Deep Space Climate Observatory (DSCOVR) are combined to yield a consistent multi-sensor record of eruptive degassing. We estimate SO2 emissions during the eruption’s key phases: the initial 19 December 2021 eruption (∼0.01 Tg SO2); continuous SO2 emissions from 20 December 2021—early January 2022 (∼0.12 Tg SO2); the 13 January 2022 stratospheric eruption (0.06 Tg SO2); and the paroxysmal 15 January 2022 eruption (∼0.4–0.5 Tg SO2); yielding a total SO2 emission of ∼0.6–0.7 Tg SO2 for the eruptive episode. We interpret the vigorous SO2 emissions observed prior to the January 2022 eruptions, which were significantly higher than measured in the 2009 and 2014 HTHH eruptions, as strong evidence for a rejuvenated magmatic system. High cadence DSCOVR/EPIC SO2 imagery permits the first UV-based analysis of umbrella cloud spreading and volume flux in the 13 January 2022 eruption, and also tracks early dispersion of the stratospheric SO2 cloud injected on January 15. The ∼0.4–0.5 Tg SO2 discharged by the paroxysmal 15 January 2022 HTHH eruption is low relative to other eruptions of similar magnitude, and a review of other submarine eruptions in the satellite era indicates that modest SO2 yields may be characteristic of submarine volcanism, with the emissions and atmospheric impacts likely dominated by water vapor. The origin of the low SO2 loading awaits further investigation but scrubbing of SO2 in the water-rich eruption plumes and rapid conversion to sulfate aerosol are plausible, given the exceptional water emission by the 15 January 2022 HTHH eruption.
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- 2022
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5. A Decade of Global Volcanic SO2 Emissions Measured from Space
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Carn, S. A, Fioletov, V. E, McLinden, C. A, Li, C, and Krotkov, N. A
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Geosciences (General) - Abstract
The global flux of sulfur dioxide (SO2) emitted by passive volcanic degassing is a key parameter that constrains the fluxes of other volcanic gases (including carbon dioxide, CO2) and toxic trace metals (e.g., mercury). It is also a required input for atmospheric chemistry and climate models, since it impacts the tropospheric burden of sulfate aerosol, a major climate-forcing species. Despite its significance, an inventory of passive volcanic degassing is very difficult to produce, due largely to the patchy spatial and temporal coverage of ground-based SO2 measurements. We report here the first volcanic SO2 emissions inventory derived from global, coincident satellite measurements, made by the Ozone Monitoring Instrument (OMI) on NASA's Aura satellite in 2005-2015. The OMI measurements permit estimation of SO2 emissions from over 90 volcanoes, including new constraints on fluxes from Indonesia, Papua New Guinea, the Aleutian Islands, the Kuril Islands and Kamchatka. On average over the past decade, the volcanic SO2 sources consistently detected from space have discharged a total of approximately 63 kt/day SO2 during passive degassing, or approximately 23 +/- 2 Tg/yr. We find that approximately 30% of the sources show significant decadal trends in SO2 emissions, with positive trends observed at multiple volcanoes in some regions including Vanuatu, southern Japan, Peru and Chile.
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- 2017
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6. Ultraviolet Satellite Measurements of Volcanic Ash
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Carn, S. A and Krotkov, N. A
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Earth Resources And Remote Sensing ,Geosciences (General) - Abstract
Ultraviolet (UV) remote sensing of volcanic ash and other absorbing aerosols from space began with the launch of the first Total Ozone Mapping Spectrometer (TOMS) instrument in 1978. Subsequent UV satellite missions (TOMS, GOME, SCIAMACHY, OMI, GOME-2, OMPS) have extended UV ash measurements to the present, generating a unique multidecadal record. A UV Aerosol Index (UVAI) based on two near-UV wavelengths, equally applicable to multispectral (TOMS, DSCOVR) or hyperspectral (GOME, SCIAMACHY, OMI, GOME-2, OMPS) instruments, has been used to derive a unique absorbing aerosol climatology across multiple UV satellite missions. Advantages of UV ash measurements relative to infrared (IR) techniques include the ability to detect ash at any altitude (assuming no clouds), above clouds, and over bright surfaces, where visible and IR techniques may fail. Disadvantages include the daytime-only restriction and nonspecificity to silicate ash, since UV measurements are sensitive to any UV-absorbing aerosol, including smoke, desert dust, and pollution. However, simultaneous retrieval of sulfur dioxide (SO2) abundance and UVAI provides robust discrimination of volcanic clouds. Although the UVAI is only semiquantitative, it has proved successful at detecting and tracking volcanic ash clouds from many volcanic eruptions since 1978. NASA A-Train measurements since 2006 (eg, CALIOP) have provided much improved constraints on volcanic ash altitude, and also permit identification of aerosol type through sensor synergy. Quantitative UV retrievals of ash optical depth, effective particle size, and ash column mass are possible and require assumptions of ash refractive index, particle size distribution, and ash layer altitude. The lack of extensive ash refractive index data in the UV-visible and the effects of ash particle shape on retrievals introduce significant uncertainty in the retrieved parameters, although limited validation against IR ash retrievals has been successful. In this contribution, we review UV ash detection and retrieval techniques and provide examples of volcanic eruptions detected in the approx. 37 year data record.
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- 2016
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7. Optimizing satellite resources for the global assessment and mitigation of volcanic hazards—Suggestions from the USGS Powell Center Volcano Remote Sensing Working Group
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Pritchard, M. E., primary, Poland, M., additional, Reath, K., additional, Andrews, B., additional, Bagnardi, M., additional, Biggs, J., additional, Carn, S., additional, Coppola, D., additional, Ebmeier, S.K., additional, Furtney, M.A., additional, Girona, T., additional, Griswold, J., additional, Lopez, T., additional, Lundgren, P., additional, Ogburn, S., additional, Pavolonis, M., additional, Rumpf, E., additional, Vaughan, G., additional, Wauthier, C., additional, Wessels, R., additional, Wright, R., additional, Anderson, K.R., additional, Bato, M.G., additional, and Roman, A., additional
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- 2022
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8. Quantifying Eruptive and Background Seismicity, Deformation, Degassing, and Thermal Emissions at Volcanoes in the United States During 1978–2020
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Reath, K., primary, Pritchard, M. E., additional, Roman, D. C., additional, Lopez, T., additional, Carn, S., additional, Fischer, T. P., additional, Lu, Z., additional, Poland, M. P., additional, Vaughan, R. G., additional, Wessels, R., additional, Wike, L. L., additional, and Tran, H. K., additional
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- 2021
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9. Modeling of 2008 Kasatochi Volcanic Sulfate Direct Radiative Forcing: Assimilation of OMI SO2 Plume Height Data and Comparison with MODIS and CALIOP Observations
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Wang, J, Park, S, Zeng, J, Ge, C, Yang, K, Carn, S, Krotkov, N, and Omar, A. H
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Earth Resources And Remote Sensing - Abstract
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 the volcanic aerosol particles. Both sensitivities highlight the need to characterize the SO2 plume height and aerosol particle size from space. While more research efforts are warranted, this study is among the first to assimilate both satellite-based SO2 plume height and amount into a chemical transport model for an improved simulation of volcanic SO2 and sulfate transport.
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- 2013
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10. Aerial strategies advance volcanic gas measurements at inaccessible, strongly degassing volcanoes
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Liu, E. J., primary, Aiuppa, A., additional, Alan, A., additional, Arellano, S., additional, Bitetto, M., additional, Bobrowski, N., additional, Carn, S., additional, Clarke, R., additional, Corrales, E., additional, de Moor, J. M., additional, Diaz, J. A., additional, Edmonds, M., additional, Fischer, T. P., additional, Freer, J., additional, Fricke, G. M., additional, Galle, B., additional, Gerdes, G., additional, Giudice, G., additional, Gutmann, A., additional, Hayer, C., additional, Itikarai, I., additional, Jones, J., additional, Mason, E., additional, McCormick Kilbride, B. T., additional, Mulina, K., additional, Nowicki, S., additional, Rahilly, K., additional, Richardson, T., additional, Rüdiger, J., additional, Schipper, C. I., additional, Watson, I. M., additional, and Wood, K., additional
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- 2020
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11. New insights into the magmatic-hydrothermal system and volatile budget of Lastarria volcano, Chile: Integrated results from the 2014 IAVCEI CCVG 12th Volcanic Gas Workshop
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Lopez, T, Aguilera, F, Tassi, F, de Moor, J, Bobrowski, N, Aiuppa, A, Tamburello, G, Rizzo, A, Liuzzo, M, Viveiros, F, Cardellini, C, Silva, C, Fischer, T, Jean-Baptiste, P, Kazayaha, R, Hidalgo, S, Malowany, K, Lucic, G, Bagnato, E, Bergsson, B, Reath, K, Liotta, M, Carn, S, Chiodini, G, Lopez T., Aguilera F., Tassi F., de Moor J.M., Bobrowski N., Aiuppa A., Tamburello G., Rizzo A, Liuzzo M., Viveiros F., Cardellini C., Silva C., Fischer T., Jean-Baptiste P., Kazayaha R., Hidalgo S., Malowany K., Lucic G., Bagnato E., Bergsson B., Reath K., Liotta M., Carn S., Chiodini G., Lopez, T, Aguilera, F, Tassi, F, de Moor, J, Bobrowski, N, Aiuppa, A, Tamburello, G, Rizzo, A, Liuzzo, M, Viveiros, F, Cardellini, C, Silva, C, Fischer, T, Jean-Baptiste, P, Kazayaha, R, Hidalgo, S, Malowany, K, Lucic, G, Bagnato, E, Bergsson, B, Reath, K, Liotta, M, Carn, S, Chiodini, G, Lopez T., Aguilera F., Tassi F., de Moor J.M., Bobrowski N., Aiuppa A., Tamburello G., Rizzo A, Liuzzo M., Viveiros F., Cardellini C., Silva C., Fischer T., Jean-Baptiste P., Kazayaha R., Hidalgo S., Malowany K., Lucic G., Bagnato E., Bergsson B., Reath K., Liotta M., Carn S., and Chiodini G.
- Abstract
Recent geophysical evidence for large-scale regional crustal inflation and localized crustal magma intrusion has made Lastarria volcano (northern Chile) the target of numerous geological, geophysical, and geochemical studies. The chemical composition of volcanic gases sampled during discrete campaigns from Lastarria volcano indicated a well-developed hydrothermal system from direct fumarole samples in A.D. 2006, 2008, and 2009, and shallow magma degassing using measurements from in situ plume sampling techniques in 2012. It is unclear if the differences in measured gas compositions and resulting interpretations were due to artifacts of the different sampling methods employed, short-term excursions from baseline due to localized changes in stress, or a systematic change in Lastarria's magmatic-hydrothermal system between 2009 and 2012. Integrated results from a two-day volcanic gas sampling and measurement campaign during the 2014 International Association of Volcanology and Chemistry of the Earth's Interior (IAVCEI) Commission on the Chemistry of Volcanic Gases (CCVG) 12th Gas Workshop are used here to compare and evaluate current gas sampling and measurement techniques, refine the existing subsurface models for Lastarria volcano, and provide new constraints on its magmatic-hydrothermal system and total degassing budget. While compositional differences among sampling methods are present, distinct compositional changes are observed, which if representative of longterm trends, indicate a change in Lastarria's overall magmatic-hydrothermal system. The composition of volcanic gases measured in 2014 contained high proportions of relatively magma- and water-soluble gases consistent with degassing of shallow magma, and in agreement with the 2012 gas composition. When compared with gas compositions measured in 2006-2009, higher relative H2O/CO2 ratios combined with lower relative CO2/St and H2O/St and stable HCl/St ratios (where St is total S [SO2 + H2S]) are observed in 20
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- 2018
12. Fog and Cloud Induced Aerosol Modification Observed by AERONET
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Eck, T. F, Holben, B. N, Reid, J. S, Giles, D. M, Rivas, M. A, Singh, R. P, Tripathi, S. N, Bruegge, C. J, Platnick, S. E, Arnold, G. T, Krotkov, N. A, Carn, S. A, Sinyuk, A, Dubovik, O, Arola, A, Schafer, J. S, Artaxo, P, Smirnov, A, Chen, H, and Goloub, P
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Meteorology And Climatology - Abstract
Large fine mode (sub-micron radius) dominated aerosols in size distributions retrieved from AERONET have been observed after fog or low-altitude cloud dissipation events. These column-integrated size distributions have been obtained at several sites in many regions of the world, typically after evaporation of low altitude cloud such as stratocumulus or fog. Retrievals with cloud processed aerosol are sometimes bimodal in the accumulation mode with the larger size mode often approx.0.4 - 0.5 microns radius (volume distribution); the smaller mode typically approx.0.12 to aprrox.0.20 microns may be interstitial aerosol that were not modified by incorporation in droplets and/or aerosol that are less hygroscopic in nature. Bimodal accumulation mode size distributions have often been observed from in situ measurements of aerosols that have interacted with clouds, and AERONET size distribution retrievals made after dissipation of cloud or fog are in good agreement with particle sizes measured by in situ techniques for cloud-processed aerosols. Aerosols of this type and large size range (in lower concentrations) may also be formed by cloud processing in partly cloudy conditions and may contribute to the shoulder of larger size particles in the accumulation mode retrievals, especially in regions where sulfate and other soluble aerosol are a significant component of the total aerosol composition. Observed trends of increasing aerosol optical depth (AOD) as fine mode radius increased suggests higher AOD in the near cloud environment and therefore greater aerosol direct radiative forcing than typically obtained from remote sensing, due to bias towards sampling at low cloud fraction.
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- 2011
13. Dispersion and Lifetime of the SO2 Cloud from the August 2008 Kasatochi Eruption
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Krotkov, N. A, Schoeberl, M. R, Morris, G. A, Carn, S, and Yang, K
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Geophysics - Abstract
Hemispherical dispersion of the SO2 cloud from the August 2008 Kasatochi eruption is analyzed using satellite data from the Ozone Monitoring Instrument (OMI) and the Goddard Trajectory Model (GTM). The operational OMI retrievals underestimate the total SO2 mass by 20-30% on 8-11 August, as compared with more accurate offline Extended Iterative Spectral Fit (EISF) retrievals, but the error decreases with time due to plume dispersion and a drop in peak SO2 column densities. The GTM runs were initialized with and compared to the operational OMI SO2 data during early plume dispersion to constrain SO2 plume heights and eruption times. The most probable SO2 heights during initial dispersion are estimated to be 10-12 km, in agreement with direct height retrievals using EISF algorithm and IR measurements. Using these height constraints a forward GTM run was initialized on 11 August to compare with the month-long Kasatochi SO2 cloud dispersion patterns. Predicted volcanic cloud locations generally agree with OMI observations, although some discrepancies were observed. Operational OMI SO2 burdens were refined using GTM-predicted mass-weighted probability density height distributions. The total refined SO2 mass was integrated over the Northern Hemisphere to place empirical constraints on the SO2 chemical decay rate. The resulting lower limit of the Kasatochi SO2 e-folding time is approx.8-9 days. Extrapolation of the exponential decay back in time yields an initial erupted SO2 mass of approx.2.2 Tg on 8 August, twice as much as the measured mass on that day.
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- 2010
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14. Insights into the 2017-2018 Ambae Eruption
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Philipson Bani, Yves Moussalam, Etienne Médard, Estelle Rose-Koga, Kenneth T. Koga, Pierre-J Gauthier, Carn, S., Aiuppa, A., Coppola, D., Tari, D., Bani, I., Mhammed Benbakkar, Voyard, G., Scott, B., Garaebiti, E., Lardy, M., Laboratoire Magmas et Volcans (LMV), Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement et la société-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Physique du Globe de Clermont-Ferrand (OPGC), Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut national des sciences de l'Univers (INSU - CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Université Jean Monnet [Saint-Étienne] (UJM), Jouhannel, Sylvaine, Institut national des sciences de l'Univers (INSU - CNRS)-Université Jean Monnet - Saint-Étienne (UJM)-Institut de Recherche pour le Développement et la société-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS)-Observatoire de Physique du Globe de Clermont-Ferrand (OPGC), and Institut national des sciences de l'Univers (INSU - CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS)
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[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/Geochemistry ,[SDU.STU.GC] Sciences of the Universe [physics]/Earth Sciences/Geochemistry ,[SDU.STU.VO] Sciences of the Universe [physics]/Earth Sciences/Volcanology ,[SDU.STU.PE]Sciences of the Universe [physics]/Earth Sciences/Petrography ,[SDU.STU.VO]Sciences of the Universe [physics]/Earth Sciences/Volcanology ,[SDU.STU.PE] Sciences of the Universe [physics]/Earth Sciences/Petrography ,ComputingMilieux_MISCELLANEOUS - Abstract
International audience
- Published
- 2019
15. The February–March 2000 eruption of Hekla, Iceland from a satellite perspective
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Rose, W. I., primary, Gu, Y., additional, Watson, I. M., additional, Yu, T., additional, Blut, G. J. S., additional, Prata, A. J., additional, Krueger, A. J., additional, Krotkov, N., additional, Carn, S., additional, Fromm, M. D., additional, Hunton, D. E., additional, Ernst, G. G. J., additional, Viggiano, A. A., additional, Miller, T. M., additional, Ballenthin, J. O., additional, Reeves, J. M., additional, Wilson, J. C., additional, Anderson, B. E., additional, and Flittner, D. E., additional
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- 2003
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16. Compilation of a Global Emission Inventory from 1980 to 2000 for Global Model Simulations of the Long-term Trend of Tropospheric Aerosols
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Diehl, T. L, Mian, Chin, Bond, T. C, Carn, S. A, Duncan, B. N, Krotkov, N. A, and Streets, D. G
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Meteorology And Climatology - Abstract
The approach to create a comprehensive emission inventory for the time period 1980 to 2000 is described in this paper. We have recently compiled an emission database, which we will use for a 21 year simulation of tropospheric aerosols with the GOCART model. Particular attention was paid to the time-dependent SO2, black carbon and organic carbon aerosol emissions. For the emission of SO2 from sporadically erupting volcanoes, we assembled emission data from the Global Volcanism Program of the Smithsonian Institution, using the VEI to derive the volcanic cloud height and the SO2 amount, and amended this dataset by the SO2 emission data from the TOMS instrument when available. 3-dimensional aircraft emission data was obtained for a number of years from the AEAP project, converted from burned fuel to SO2 and interpolated to each year, taking the sparsity of the flight patterns into account. Other anthopogenic SO2 emissions are based on gridded emissions from the EDGAR 2000 database (excluding sources from aircraft, biomass burning and international ship traffic), which were scaled to individual years with country/regional based emission inventories. Gridded SO2 emissions from international ship traffic for 2000 and the scaling factors for other years are from [Eyring et al., 2005]. We used gridded anthropogenic black and organic carbon emissions for 1996 [Bond et al., 2005], again excluding aircraft, biomass burning and ship sources. These emissions were scaled with regional based emission inventories from 1980 to 2000 to derive gridded emissions for each year. The biomass burning emissions are based on a climatology, which is scaled with regional scaling factors derived from the TOMS aerosol index and the AVHRR/ATSR fire counts to each year [Duncan et al., 2003]. Details on the integration of the information from the various sources will be provided and the distribution patterns and total emissions in the final product will be discussed.
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- 2007
17. Petrology and Geochemistry of the Lamongan Volcanic Field, East Java, Indonesia: Primitive Sunda Arc Magmas in an Extensional Tectonic Setting?
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Carn, S. A. and Pyle, D. M.
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- 2001
18. Thermal, deformation, and degassing remote sensing time‐series (A.D. 2000‐2017) at the 47 most active volcanoes in Latin America: Implications for volcanic systems
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Reath, K, Pritchard, M, Poland, M, Delgado, F, Carn, S, Coppola, D, Andrews, B, Ebmeier, SK, Rumpf, E, Henderson, S, Baker, S, Lundgren, P, Wright, R, Biggs, J, Lopez, T, Wauthier, C, Moruzzi, S, Alcott, A, Wessels, R, Griswold, J, Ogburn, S, Loughlin, S, Meyer, F, Vaughan, G, and Bagnardi, M
- Abstract
Volcanoes are hazardous to local and global populations, but only a fraction are continuously monitored by ground‐based sensors. For example, in Latin America, more than 60% of Holocene volcanoes are unmonitored, meaning long‐term multi‐parameter datasets of volcanic activity are rare and sparse. We use satellite observations of degassing, thermal anomalies, and surface deformation spanning 17 years at 47 of the most active volcanoes in Latin America, and compare these datasets to ground‐based observations archived by the Global Volcanism Program (GVP). This first comparison of multi‐satellite time‐series on a regional scale provides information regarding volcanic behavior during, non‐, pre‐, syn‐ and post‐eruptive periods. For example, at Copahue volcano, deviations from background activity in all three types of satellite measurements were manifested months to years in advance of renewed eruptive activity in 2012. By quantifying the amount of degassing, thermal output, and deformation measured at each of these volcanoes, we test the classification of these volcanoes as open or closed volcanic systems. We find that ~28% of the volcanoes do not fall into either classification and the rest show elements of both, demonstrating a dynamic range of behavior that can change over time. Finally, we recommend how volcano monitoring could be improved through better coordination of available satellite‐based capabilities and new instruments.
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- 2019
19. Thermal, deformation, and degassing remote sensing time series (CE 2000-2017) at the 47 most active volcanoes in Latin America: implications for volcanic systems
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Reath, K., Pritchard, M., Poland, M., Delgado, F., Carn, S., Coppola, D., Andrews, B., Ebmeier, S.K., Rumpf, E., Henderson, S., Baker, S., Lundgren, P., Wright, R., Biggs, J., Lopez, T., Wauthier, C., Moruzzi, S., Alcott, A., Wessels, R., Griswold, J., Ogburn, S., Loughlin, S., Meyer, F., Vaughan, G., Bagnardi, M., Reath, K., Pritchard, M., Poland, M., Delgado, F., Carn, S., Coppola, D., Andrews, B., Ebmeier, S.K., Rumpf, E., Henderson, S., Baker, S., Lundgren, P., Wright, R., Biggs, J., Lopez, T., Wauthier, C., Moruzzi, S., Alcott, A., Wessels, R., Griswold, J., Ogburn, S., Loughlin, S., Meyer, F., Vaughan, G., and Bagnardi, M.
- Abstract
Volcanoes are hazardous to local and global populations, but only a fraction are continuously monitored by ground‐based sensors. For example, in Latin America, more than 60% of Holocene volcanoes are unmonitored, meaning long‐term multiparameter data sets of volcanic activity are rare and sparse. We use satellite observations of degassing, thermal anomalies, and surface deformation spanning 17 years at 47 of the most active volcanoes in Latin America and compare these data sets to ground‐based observations archived by the Global Volcanism Program. This first comparison of multisatellite time series on a regional scale provides information regarding volcanic behavior during, noneruptive, pre‐eruptive, syneruptive, and posteruptive periods. For example, at Copahue volcano, deviations from background activity in all three types of satellite measurements were manifested months to years in advance of renewed eruptive activity in 2012. By quantifying the amount of degassing, thermal output, and deformation measured at each of these volcanoes, we test the classification of these volcanoes as open or closed volcanic systems. We find that ~28% of the volcanoes do not fall into either classification, and the rest show elements of both, demonstrating a dynamic range of behavior that can change over time. Finally, we recommend how volcano monitoring could be improved through better coordination of available satellite‐based capabilities and new instruments.
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- 2019
20. Volcanic Cloud and Aerosol Monitor (VOLCAM) for Deep Space Gateway
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Krotkov, N., Bhartia, P. K., Torres, O., Li, C., Sanders, S., Realmuto, V., Carn, S., and Herman, J.
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combined use of UV and TIR cameras ,ultraviolet (UV) filter camera ,whole earth imaging ,Thermal Infrared (TIR) filter camera ,atmospheric composition retrievals - Abstract
Deep Space Gateway Science Workshop 2018 (LPI Contrib. No. 2063) This work was written as part of one of the atuthor's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law., Frequent (~15 min) imaging of reflected solar ultra-violet (UV) and thermal ifrared (TIR) radiation of the whole Earth from cislunar vantage point offer unique possibilities to answer NASA’s Earth System Science (ESS) questions and further advance volcanic ash (VA) and sulfur dioxide (VSO2) aviation safety applications. We propose complementary ultraviolet (UV) and ther-mal Infrared (TIR) filter cameras for a dual-purpose whole Earth imaging with complementary natural haz-ards applications and Earth System science goals.
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- 2018
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21. Thermal, Deformation, and Degassing Remote Sensing Time Series (CE 2000–2017) at the 47 most Active Volcanoes in Latin America: Implications for Volcanic Systems
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Reath, K., primary, Pritchard, M., additional, Poland, M., additional, Delgado, F., additional, Carn, S., additional, Coppola, D., additional, Andrews, B., additional, Ebmeier, S. K., additional, Rumpf, E., additional, Henderson, S., additional, Baker, S., additional, Lundgren, P., additional, Wright, R., additional, Biggs, J., additional, Lopez, T., additional, Wauthier, C., additional, Moruzzi, S., additional, Alcott, A., additional, Wessels, R., additional, Griswold, J., additional, Ogburn, S., additional, Loughlin, S., additional, Meyer, F., additional, Vaughan, G., additional, and Bagnardi, M., additional
- Published
- 2019
- Full Text
- View/download PDF
22. First Observations of Volcanic Eruption Clouds From the L1 Earth‐Sun Lagrange Point by DSCOVR/EPIC
- Author
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Carn, S. A., primary, Krotkov, N. A., additional, Fisher, B. L., additional, Li, C., additional, and Prata, A. J., additional
- Published
- 2018
- Full Text
- View/download PDF
23. A multidisciplinary study of the final episode of the Manda Hararo dyke sequence, Ethiopia, and implications for trends in volcanism during the rifting cycle
- Author
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Barnie, T. D., Keir, D., Hamling, I., Hofmann, B., Belachew, M., Carn, S., Eastwell, D., Hammond, J. O. S., Ayele, A., Oppenheimer, C., and Wright, T. J.
- Subjects
Magma, rifting, Afar - Published
- 2016
24. Special publication - Geological Society of London
- Author
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Harris, A. J. L., Carn, S., Dehn, J., Del Negro, C., Gudmundsson, M. T., Cordonnier, B., Barnie, T., Chahi, E., Calvari, S., Catry, T., De Groeve, T., Coppola, D., Davies, A., Favalli, M., Ferrucci, F., Fujita, E., Ganci, G., Garel, F., Huet, P., Kauahikaua, J., Kelfoun, K., Lombardo, V., Macedonio, G., Pacheco, J., Patrick, M., Pergola, N., Ramsey, M., Rongo, R., Sahy, F., Smith, K., Tarquini, S., Thordarson, T., Villeneuve, N., Webley, P., Wright, R., and Zaksek, K.
- Subjects
ROBUST SATELLITE TECHNIQUES ,MOUNT-ETNA ,TEMPERATURE-FIELD ,ACTIVE VOLCANOS ,KILAUEA VOLCANO ,FIELD OBSERVATIONS ,CELLULAR-AUTOMATA MODEL ,SPATIAL-RESOLUTION ,LAVA FLOW HAZARD ,STROMBOLI VOLCANO - Abstract
RED SEED stands for Risk Evaluation, Detection and Simulation during Effusive Eruption Disasters, and combines stakeholders from the remote sensing, modelling and response communities with experience in tracking volcanic effusive events. The group first met during a three day-long workshop held in Clermont Ferrand (France) between 28 and 30 May 2013. During each day, presentations were given reviewing the state of the art in terms of (a) volcano hot spot detection and parameterization, (b) operational satellite-based hot spot detection systems, (c) lava flow modelling and (d) response protocols during effusive crises. At the end of each presentation set, the four groups retreated to discuss and report on requirements for a truly integrated and operational response that satisfactorily combines remote sensors, modellers and responders during an effusive crisis. The results of collating the final reports, and follow-up discussions that have been on-going since the workshop, are given here. We can reduce our discussions to four main findings. (1) Hot spot detection tools are operational and capable of providing effusive eruption onset notice within 15 min. (2) Spectral radiance metrics can also be provided with high degrees of confidence. However, if we are to achieve a truly global system, more local receiving stations need to be installed with hot spot detection and data processing modules running on-site and in real time. (3) Models are operational, but need real-time input of reliable time-averaged discharge rate data and regular updates of digital elevation models if they are to be effective; the latter can be provided by the radar/photogrammetry community. (4) Information needs to be provided in an agreed and standard format following an ensemble approach and using models that have been validated and recognized as trustworthy by the responding authorities. All of this requires a sophisticated and centralized data collection, distribution and reporting hub that is based on a philosophy of joint ownership and mutual trust. While the next chapter carries out an exercise to explore the viability of the last point, the detailed recommendations behind these findings are detailed here.
- Published
- 2016
- Full Text
- View/download PDF
25. A multidisciplinary study of the final episode of the Manda Hararo dyke sequence, Ethiopia, and implications for trends in volcanism during the rifting cycle
- Author
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Barnie, T.D., Keir, D., Hamling, I., Hofmann, B., Belachew, M., Carn, S., Eastwell, D., Hammond, James O.S., Ayele, A., Oppenheimer, C., Wright, T., Wright, T.J., Ayele, A., Ferguson, D.J., Kidane, T., and Vye-Brown, C.
- Subjects
es - Abstract
The sequence of dyke intrusions between 2005 and 2010 in the Manda Hararo rift segment, Ethiopia, provided an opportunity to test conceptual models of continental rifting. Based on trends up to dyke 13 in the sequence, it was anticipated that, should magma supply con- tinue, dykes would shorten in length and eruptions would increase in size and decrease in distance from the segment centre as extensional stress was progressively released. In this paper we revisit these predictions by presenting a comprehensive overview of the May 2010 dyke and fissure erup- tion, the 14th and last in the sequence, from InSAR, seismicity, satellite thermal data, ultraviolet SO2 retrievals and multiple LiDAR surveys. We find the dyke is longer than other eruptive dykes in the sequence, propagating in two directions from the segment centre, but otherwise fairly typical in terms of opening, propagation speed and geodetic and seismic moment. However, though the eruption is located closer to the segment centre, it is much smaller than pre- vious events. We interpret this as indicating that either the Manda Hararo rifting event was magma limited, or that extensional stress varies north and south of the segment centre.
- Published
- 2016
26. In situ measurements of tropospheric volcanic plumes in Ecuador and Colombia during TC^4
- Author
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Carn, S. A., Froyd, K. D., Anderson, B. E., Wennberg, P., Crounse, J., Spencer, K., Dibb, J. E., Krotkov, N. A., Browell, E. V., Hair, J. W., Diskin, G., Sachse, G., and Vay, S. A.
- Abstract
A NASA DC-8 research aircraft penetrated tropospheric gas and aerosol plumes sourced from active volcanoes in Ecuador and Colombia during the Tropical Composition, Cloud and Climate Coupling (TC^4) mission in July–August 2007. The likely source volcanoes were Tungurahua (Ecuador) and Nevado del Huila (Colombia). The TC^4 data provide rare insight into the chemistry of volcanic plumes in the tropical troposphere and permit a comparison of SO_2 column amounts measured by the Ozone Monitoring Instrument (OMI) on the Aura satellite with in situ SO_2 measurements. Elevated concentrations of SO_2, sulfate aerosol, and particles were measured by DC-8 instrumentation in volcanic outflow at altitudes of 3–6 km. Estimated plume ages range from ~2 h at Huila to ~22–48 h downwind of Ecuador. The plumes contained sulfate-rich accumulation mode particles that were variably neutralized and often highly acidic. A significant fraction of supermicron volcanic ash was evident in one plume. In-plume O_3 concentrations were ~70%–80% of ambient levels downwind of Ecuador, but data are insufficient to ascribe this to O_3 depletion via reactive halogen chemistry. The TC^4 data record rapid cloud processing of the Huila volcanic plume involving aqueous-phase oxidation of SO_2 by H_2O_2, but overall the data suggest average in-plume SO_2 to sulfate conversion rates of ~1%–2% h^(−1). SO_2 column amounts measured in the Tungurahua plume (~0.1–0.2 Dobson units) are commensurate with average SO_2 columns retrieved from OMI measurements in the volcanic outflow region in July 2007. The TC^4 data set provides further evidence of the impact of volcanic emissions on tropospheric acidity and oxidizing capacity.
- Published
- 2011
27. On the detection and monitoring of effusive eruptions using satellite SO 2 measurements
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Carn, S. A., primary
- Published
- 2016
- Full Text
- View/download PDF
28. Conclusion: recommendations and findings of the RED SEED working group
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Harris, A. J. L., primary, Carn, S., additional, Dehn, J., additional, Del Negro, C., additional, Guđmundsson, M. T., additional, Cordonnier, B., additional, Barnie, T., additional, Chahi, E., additional, Calvari, S., additional, Catry, T., additional, de Groeve, T., additional, Coppola, D., additional, Davies, A., additional, Favalli, M., additional, Ferrucci, F., additional, Fujita, E., additional, Ganci, G., additional, Garel, F., additional, Huet, P., additional, Kauahikaua, J., additional, Kelfoun, K., additional, Lombardo, V., additional, Macedonio, G., additional, Pacheco, J., additional, Patrick, M., additional, Pergola, N., additional, Ramsey, M., additional, Rongo, R., additional, Sahy, F., additional, Smith, K., additional, Tarquini, S., additional, Thordarson, T., additional, Villeneuve, N., additional, Webley, P., additional, Wright, R., additional, and Zakšek, K., additional
- Published
- 2016
- Full Text
- View/download PDF
29. Properties of Sarychev sulphate aerosols over the Arctic
- Author
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O'Neill, Norm T., Perro, C., Saha, A., Lesins, G., Duck, T. J., Eloranta, E. W., Nott, G. J., Hoffmann, Anne, Ritter, Christoph, Karmudi, M.L., Bourassa, A., Abboud, I., Carn, S. A., and Savatiouk, V
- Abstract
Aerosols from the Sarychev Peak volcano entered the Arctic region less than a week after the strongest SO2eruption on June 15 and 16, 2009 and had, by the first week in July, spread out over the entire Arctic region. These predominantly stratospheric aerosols were determined to be sub-micron in size and inferred to be composed of sulphates produced from the condensation of SO2gases emitted during the eruption. Average (500 nm) Sarychev-induced stratospheric optical depths (SOD) over the Polar Environmental Atmospheric Research Laboratory (PEARL) at Eureka (Nunavut, Canada) were found to be between 0.03 and 0.05 during the months of July and August, 2009. This estimate, derived from sunphotometry and integrated lidar backscatter profiles was consistent with averages derived from lidar estimates over Ny-Ålesund (Spitsbergen). The Sarychev SOD e-folding time at Eureka, deduced from lidar profiles, was found to be approximately 4 months relative to a regression start date of July 27. These profiles initially revealed the presence of multiple Sarychev plumes between the tropopause and about 17 km altitude. After about two months, the complex vertical plume structures had collapsed into fewer, more homogeneous plumes located near the tropopause. It was found that the noisy character of daytime backscatter returns induced an artifactual minimum in the temporal, pan-Arctic, CALIOP SOD response to Sarychev sulphates. A depolarization ratio discrimination criterion was used to separate the CALIOP stratospheric layer class into a low depolarization subclass which was more representative of Sarychev sulphates. Post-SAT (post Sarychev Arrival Time) retrievals of the fine mode effective radius (reff,f) and the logarithmic standard deviation for two Eureka sites and Thule (Greenland) were all close to 0.25 μm and 1.6 respectively. The stratospheric analogue to the columnar reff,f average was estimated to be reff,f(+) = 0.29 μm for Eureka data. Stratospheric, Raman lidar retrievals at Ny-Ålesund, yielded a post-SAT average of reff,f(+) = 0.27 μm. These results are ∼50% larger than the background stratospheric-aerosol value. They are also about a factor of two larger than modeling values used in recent publications or about a factor of five larger in terms of (per particle) backscatter cross section.
- Published
- 2010
30. A multidisciplinary study of the final episode of the Manda Hararo dyke sequence, Ethiopia, and implications for trends in volcanism during the rifting cycle
- Author
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Barnie, T. D., primary, Keir, D., additional, Hamling, I., additional, Hofmann, B., additional, Belachew, M., additional, Carn, S., additional, Eastwell, D., additional, Hammond, J. O. S., additional, Ayele, A., additional, Oppenheimer, C., additional, and Wright, T., additional
- Published
- 2015
- Full Text
- View/download PDF
31. Extended observations of volcanic SO2 and sulfate aerosol in the stratosphere
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Carn, S. A., Krotkov, N. A., Yang, K., Hoff, R. M., Prata, A. J., Krueger, A. J., Loughlin, S. C., Levelt, P. F., and EGU, Publication
- Subjects
[SDU.OCEAN] Sciences of the Universe [physics]/Ocean, Atmosphere - Abstract
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 that reveal the composition, structure and longevity of a stratospheric SO2 cloud and derived sulfate layer following a modest eruption (0.2 Tg total SO2) of Soufriere Hills volcano, Montserrat on 20 May 2006. The SO2 cloud alone was tracked for over 3 weeks and a distance of over 20 000 km; unprecedented for an eruption of this size. Derived sulfate aerosol at an altitude of ~20 km had circled the globe by 22 June and remained visible in CALIPSO data until at least 6 July. These synergistic NASA A-Train observations permit a new appreciation of the potential effects of frequent, small-to-moderate volcanic eruptions on stratospheric composition and climate.
- Published
- 2007
32. Extreme rates of sulphur and halogen degassing from Ambryn volcano, Vanuatu
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Bani, P., Oppenheimer, C., Tsanev, V.-I., Carn, S.-A.-A., Cronin, S.-J., Crimp, R., Calkins, J.-A., Charley, D., Lardy, M., Pôle Pluridisciplinaire de la Matière et de l'Environnement (PPME), Université de la Nouvelle-Calédonie (UNC), and BUNC, Pole ID
- Subjects
[SDU.STU.VO] Sciences of the Universe [physics]/Earth Sciences/Volcanology ,[SDU.STU.VO]Sciences of the Universe [physics]/Earth Sciences/Volcanology ,ComputingMilieux_MISCELLANEOUS - Abstract
International audience
- Published
- 2006
33. Extending the long-term record of volcanic SO2emissions with the Ozone Mapping and Profiler Suite nadir mapper
- Author
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Carn, S. A., primary, Yang, K., additional, Prata, A. J., additional, and Krotkov, N. A., additional
- Published
- 2015
- Full Text
- View/download PDF
34. Stratospheric volcanic ash emissions from the 13 February 2014 Kelut eruption
- Author
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Kristiansen, N. I., primary, Prata, A. J., additional, Stohl, A., additional, and Carn, S. A., additional
- Published
- 2015
- Full Text
- View/download PDF
35. An innovative application of the kinect in earth sciences: Quantifying deformation in analogue modelling of volcanoes
- Author
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Tortini, R, Bonali, F, Corazzato, C, Carn, S, Tibaldi, A, BONALI, FABIO LUCA, CORAZZATO, CLAUDIA, TIBALDI, ALESSANDRO, Tortini, R, Bonali, F, Corazzato, C, Carn, S, Tibaldi, A, BONALI, FABIO LUCA, CORAZZATO, CLAUDIA, and TIBALDI, ALESSANDRO
- Abstract
Measuring surface deformation is critical in analogue modelling of Earth science phenomena. Here, we present a novel application of the Microsoft Kinect sensor to measure vertical deformation in a scaled analogue model of Nisyros volcano (Greece), simulating two magmatic sources and related surface deformation. The Kinect permits capture of real time, 640 × 480 pixel, true-colour images (RGB) and a grid of distances to the modelled surface with a horizontal and vertical resolution of ±1 mm. Using recorded distances permits quantification of vertical deformation in terms of maximum and average down- and uplift during deflation and inflation phases respectively, which is of crucial importance for defining the kinematics of faults formed during the modelling, determined from interpretation of the RGB images. Although other techniques have demonstrated similar or higher accuracy, our study demonstrates the cost-effectiveness of the Kinect in analogue modelling of volcanoes. © 2014 John Wiley & Sons Ltd.
- Published
- 2014
36. The sulfur budget of the 2011 Grimsvötn eruption, Iceland
- Author
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Sigmarsson, O., Haddadi, B., Carn, S., Moune, S., Gudnason, J., Yang, K.D., Clarisse, Lieven, Sigmarsson, O., Haddadi, B., Carn, S., Moune, S., Gudnason, J., Yang, K.D., and Clarisse, Lieven
- Abstract
Sulfur concentrations have been measured in 28 melt inclusions (MIs) in plagioclase, clinopyroxene, and olivine crystals extracted from tephra produced during the explosive eruption of Grímsvötn in May 2011. The results are compared to sulfur concentrations in the groundmass glass in order to estimate the mass of sulfur brought to surface during the eruption. Satellite measurements yield order of magnitude lower sulfur (~0.2 Tg) in the eruption plume than estimated from the difference between MI and the groundmass glass. This sulfur "deficit" is readily explained by sulfur adhering to tephra grains but principally by sulfide globules caused by basalt-sulfide melt exsolution before degassing. A mass balance calculation reveals that approximately ~0.8 Tg of SO2 is present as globules, representing ~50% of the total sulfur budget. Most of the sulfide globules likely reside at depth due to their elevated density, for potential later remobilization by new magma or hydrothermal circulation. Key Points H2S and SO2 degassing is estimated for the 2011 eruption of Grímsvötn Satellite-based SO2 mass loading is lower than from mineral melt inclusions Half of S resides as sulfide globules; 25% enter the stratosphere ©2013. American Geophysical Union. All Rights Reserved., SCOPUS: ar.j, FLWIN, info:eu-repo/semantics/published
- Published
- 2013
37. Quantifying Deformation in Volcano Analogue Modelling: an Innovative Application of the KinectTM Sensor
- Author
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Tortini, R, Bonali, F, Corazzato, C, Carn, S, Tibaldi, A, Bonali FL, Carn, SA, Tortini, R, Bonali, F, Corazzato, C, Carn, S, Tibaldi, A, Bonali FL, and Carn, SA
- Published
- 2013
38. Properties of Sarychev sulphate aerosols over the Arctic
- Author
-
O'Neill, Norm T., Perro, C., Saha, A., Lesins, G., Duck, T. J., Eloranta, E. W., Nott, G. J., Hoffmann, Anne, Ritter, Christoph, Karmudi, M.L., Bourassa, A., Abboud, I., Carn, S. A., Savatiouk, V, O'Neill, Norm T., Perro, C., Saha, A., Lesins, G., Duck, T. J., Eloranta, E. W., Nott, G. J., Hoffmann, Anne, Ritter, Christoph, Karmudi, M.L., Bourassa, A., Abboud, I., Carn, S. A., and Savatiouk, V
- Abstract
Aerosols from the Sarychev Peak volcano entered the Arctic region less than a week after the strongest SO2eruption on June 15 and 16, 2009 and had, by the first week in July, spread out over the entire Arctic region. These predominantly stratospheric aerosols were determined to be sub-micron in size and inferred to be composed of sulphates produced from the condensation of SO2gases emitted during the eruption. Average (500 nm) Sarychev-induced stratospheric optical depths (SOD) over the Polar Environmental Atmospheric Research Laboratory (PEARL) at Eureka (Nunavut, Canada) were found to be between 0.03 and 0.05 during the months of July and August, 2009. This estimate, derived from sunphotometry and integrated lidar backscatter profiles was consistent with averages derived from lidar estimates over Ny-Ålesund (Spitsbergen). The Sarychev SOD e-folding time at Eureka, deduced from lidar profiles, was found to be approximately 4 months relative to a regression start date of July 27. These profiles initially revealed the presence of multiple Sarychev plumes between the tropopause and about 17 km altitude. After about two months, the complex vertical plume structures had collapsed into fewer, more homogeneous plumes located near the tropopause. It was found that the noisy character of daytime backscatter returns induced an artifactual minimum in the temporal, pan-Arctic, CALIOP SOD response to Sarychev sulphates. A depolarization ratio discrimination criterion was used to separate the CALIOP stratospheric layer class into a low depolarization subclass which was more representative of Sarychev sulphates. Post-SAT (post Sarychev Arrival Time) retrievals of the fine mode effective radius (reff,f) and the logarithmic standard deviation for two Eureka sites and Thule (Greenland) were all close to 0.25 μm and 1.6 respectively. The stratospheric analogue to the columnar reff,f average was estimated to be reff,f(+) = 0.29 μm for Eureka data. Stratospheric, Raman lidar retrievals
- Published
- 2012
39. Fog- and Cloud-Induced Aerosol Modification Observed by the Aerosol Robotic Network (AERONET)
- Author
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Eck, T. F., Holben, B. N., Reid, J. S., Giles, D. M., Rivas, M. A., Singh, Ramesh P., Tripathi, S. N., Bruegge, C. J., Platnick, S., Arnold, G. T., Krotkov, N. A., Carn, S. A., Sinyuk, A., Dubovik, O., Arola, A., Schafer, J. S., Artaxo, P., Smirnov, A., Chen, H., Goloub, P., Eck, T. F., Holben, B. N., Reid, J. S., Giles, D. M., Rivas, M. A., Singh, Ramesh P., Tripathi, S. N., Bruegge, C. J., Platnick, S., Arnold, G. T., Krotkov, N. A., Carn, S. A., Sinyuk, A., Dubovik, O., Arola, A., Schafer, J. S., Artaxo, P., Smirnov, A., Chen, H., and Goloub, P.
- Abstract
Large fine mode-dominated aerosols (submicron radius) in size distributions retrieved from the Aerosol Robotic Network (AERONET) have been observed after fog or low-altitude cloud dissipation events. These column-integrated size distributions have been obtained at several sites in many regions of the world, typically after evaporation of low-altitude cloud such as stratocumulus or fog. Retrievals with cloud-processed aerosol are sometimes bimodal in the accumulation mode with the larger-size mode often similar to 0.4-0.5 mu m radius (volume distribution); the smaller mode, typically similar to 0.12 to similar to 0.20 mu m, may be interstitial aerosol that were not modified by incorporation in droplets and/or aerosol that are less hygroscopic in nature. Bimodal accumulation mode size distributions have often been observed from in situ measurements of aerosols that have interacted with clouds, and AERONET size distribution retrievals made after dissipation of cloud or fog are in good agreement with particle sizes measured by in situ techniques for cloud-processed aerosols. Aerosols of this type and large size range (in lower concentrations) may also be formed by cloud processing in partly cloudy conditions and may contribute to the "shoulder" of larger-size particles in the accumulation mode retrievals, especially in regions where sulfate and other soluble aerosol are a significant component of the total aerosol composition. Observed trends of increasing aerosol optical depth (AOD) as fine mode radius increased suggests higher AOD in the near-cloud environment and higher overall AOD than typically obtained from remote sensing owing to bias toward sampling at low cloud fraction.
- Published
- 2012
40. Properties of Sarychev sulphate aerosols over the Arctic
- Author
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O'Neill, N. T., Perro, C., Saha, A., Lesins, G., Duck, T. J., Eloranta, E. W., Nott, G. J., Hoffmann, Anne, Karumudi, M. L., Ritter, Christoph, Bourassa, A., Abboud, I., Carn, S. A., Savastiouk, V., O'Neill, N. T., Perro, C., Saha, A., Lesins, G., Duck, T. J., Eloranta, E. W., Nott, G. J., Hoffmann, Anne, Karumudi, M. L., Ritter, Christoph, Bourassa, A., Abboud, I., Carn, S. A., and Savastiouk, V.
- Abstract
Aerosols from the Sarychev Peak volcano entered the Arctic region less than a week after the strongest SO2 eruption on June 15 and 16, 2009 and had, by the second week in July, spread out over the entire Arctic region. These predominantly stratospheric aerosols were determined to be sub-micron in size and inferred to be composed of sulphates produced from the condensation of SO2 gases emitted during the eruption. Average (500 nm) Sarychev-induced stratospheric optical depths over the Polar Environmental Atmospheric Research Laboratory (PEARL) at Eureka, Nunavut, Canada were found to be between 0.03 and 0.05 during the months of July and August, 2009. This estimate, derived from sunphotometry and integrated lidar backscatter profiles was consistent with averages derived from lidar estimates over Ny-Ålesund (Spitsbergen). The Sarychev SOD e-folding time at Eureka, deduced from lidar profiles, was found to be approximately 4 months relative to a regression start date of July 27. These profiles initially revealed the presence of multiple Sarychev plumes between the tropopause and about 17 km altitude. After about two months, the complex vertical plume structures had collapsed into fewer, more homogeneous plumes located near the tropopause. It was found that the noisy character of daytime backscatter returns induced an artifactual minimum in the temporal, pan-Arctic, CALIOP SOD response to Sarychev sulphates. A depolarization ratio discrimination criterion was used to separate the CALIOP stratospheric layer class into a low depolarization subclass which was more representative of Sarychev sulphates. Post-SAT (post Sarychev Arrival Time) retrievals of the fine mode effective radius (reff,f) and the logarithmic standard deviation for two Eureka sites and Thule, Greenland were all close to 0.25 μm and 1.6 respectively. The stratospheric analogue to the columnar reff,f average was estimated to be reff,f(+) = 0.29 μm for Eureka data. Stratospheric, Raman lidar retrievals at N
- Published
- 2010
41. Validation of SO2 retrievals from the Ozone Monitoring Instrument (OMI) over NE China
- Author
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Krotkov, N. A., Krotkov, N. A., McClure, B., Dickerson, R. R., Carn, S., Li, C., Bhartia, P. K., Yang, K., Krueger, A., Li, Z., Levelt, P. F., Chen, Hongbin, Wang, Pucai, Lu, Daren, Krotkov, N. A., Krotkov, N. A., McClure, B., Dickerson, R. R., Carn, S., Li, C., Bhartia, P. K., Yang, K., Krueger, A., Li, Z., Levelt, P. F., Chen, Hongbin, Wang, Pucai, and Lu, Daren
- Abstract
The Ozone Monitoring Instrument (OMI) launched on the NASA Aura satellite in July 2004 offers unprecedented spatial resolution, coupled with contiguous daily global coverage, for space-based UV measurements of sulfur dioxide (SO2). We present a first validation of the OMI SO2 data with in-situ aircraft measurements in NE China in April 2005. The study demonstrates that OMI can distinguish between background SO2 conditions and heavy pollution on a daily basis. The noise (expressed as the standard deviation, σ) in the PBL SO2 data is ~1.5DU (Dobson Unit, 2.691016 molecules/cm2) for instantaneous field of view (IFOV) data. By looking at the pristine South Pacific under optimal conditions we have determined that temporal and spatial averaging can improve the resolution of the instrument to σ ~ 0.3 DU; the long term average over this remote location was within 0.1 DU of zero. Under polluted conditions, however, Collection 2 data are higher than aircraft measurements by a factor of two in most cases. Parameterization of the airmass factor (AMF) appears to enhance the accuracy of the SO2 data. Improved calibrations of the radiance and irradiance data (Collection 3) result in better agreement with aircraft measurements on polluted days. The re-processed and AMF-corrected Collection 3 data still show positive bias and sensitivity to UV absorbing aerosols. The difference between the in situ data and the OMI daily PBL SO2 measurements within 30 km of the aircraft profiles was about 1 DU, equivalent to ~5 ppb from 0 to 3000 m altitude. Quantifying the SO2 profile and spectral dependence of aerosol absorption between 310 and 330 nm are critical for accurate estimates of SO2 from satellite UV measurements.
- Published
- 2008
42. Measuring global volcanic degassing with the Ozone Monitoring Instrument (OMI)
- Author
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Carn, S. A., primary, Krotkov, N. A., additional, Yang, K., additional, and Krueger, A. J., additional
- Published
- 2013
- Full Text
- View/download PDF
43. Modeling of 2008 Kasatochi volcanic sulfate direct radiative forcing: assimilation of OMI SO<sub>2</sub> plume height data and comparison with MODIS and CALIOP observations
- Author
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Wang, J., primary, Park, S., additional, Zeng, J., additional, Yang, K., additional, Carn, S., additional, Krotkov, N., additional, and Omar, A. H., additional
- Published
- 2012
- Full Text
- View/download PDF
44. Using horizontal transport characteristics to infer an emission height time series of volcanic SO2
- Author
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Hughes, E. J., primary, Sparling, L. C., additional, Carn, S. A., additional, and Krueger, A. J., additional
- Published
- 2012
- Full Text
- View/download PDF
45. Fog‐ and cloud‐induced aerosol modification observed by the Aerosol Robotic Network (AERONET)
- Author
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Eck, T. F., primary, Holben, B. N., additional, Reid, J. S., additional, Giles, D. M., additional, Rivas, M. A., additional, Singh, R. P., additional, Tripathi, S. N., additional, Bruegge, C. J., additional, Platnick, S., additional, Arnold, G. T., additional, Krotkov, N. A., additional, Carn, S. A., additional, Sinyuk, A., additional, Dubovik, O., additional, Arola, A., additional, Schafer, J. S., additional, Artaxo, P., additional, Smirnov, A., additional, Chen, H., additional, and Goloub, P., additional
- Published
- 2012
- Full Text
- View/download PDF
46. Properties of Sarychev sulphate aerosols over the Arctic
- Author
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O'Neill, N. T., primary, Perro, C., additional, Saha, A., additional, Lesins, G., additional, Duck, T. J., additional, Eloranta, E. W., additional, Nott, G. J., additional, Hoffman, A., additional, Karumudi, M. L., additional, Ritter, C., additional, Bourassa, A., additional, Abboud, I., additional, Carn, S. A., additional, and Savastiouk, V., additional
- Published
- 2012
- Full Text
- View/download PDF
47. Opportunistic validation of sulfur dioxide in the Sarychev Peak volcanic eruption cloud
- Author
-
Carn, S. A., primary and Lopez, T. M., additional
- Published
- 2011
- Full Text
- View/download PDF
48. Supplementary material to "Opportunistic validation of sulfur dioxide in the Sarychev Peak volcanic eruption cloud"
- Author
-
Carn, S. A., primary and Lopez, T. M., additional
- Published
- 2011
- Full Text
- View/download PDF
49. In situ measurements of tropospheric volcanic plumes in Ecuador and Colombia during TC4
- Author
-
Carn, S. A., primary, Froyd, K. D., additional, Anderson, B. E., additional, Wennberg, P., additional, Crounse, J., additional, Spencer, K., additional, Dibb, J. E., additional, Krotkov, N. A., additional, Browell, E. V., additional, Hair, J. W., additional, Diskin, G., additional, Sachse, G., additional, and Vay, S. A., additional
- Published
- 2011
- Full Text
- View/download PDF
50. Dispersion and lifetime of the SO2cloud from the August 2008 Kasatochi eruption
- Author
-
Krotkov, N. A., primary, Schoeberl, M. R., additional, Morris, G. A., additional, Carn, S., additional, and Yang, K., additional
- Published
- 2010
- Full Text
- View/download PDF
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