scholarly journals Lava Volume from Remote Sensing Data: Comparisons with Reverse Petrological Approaches for Two Types of Effusive Eruption

2022 ◽  
Vol 14 (2) ◽  
pp. 323
Author(s):  
Pauline Verdurme ◽  
Simon Carn ◽  
Andrew J. L. Harris ◽  
Diego Coppola ◽  
Andrea Di Muro ◽  
...  

Five effusive eruptions of Piton de la Fournaise (La Réunion) are analyzed to investigate temporal trends of erupted mass and sulfur dioxide (SO2) emissions. Daily SO2 emissions are acquired from three ultraviolet (UV) satellite instruments (the Ozone Monitoring Instrument (OMI), the Ozone Mapping and Profiler Suite (OMPS), and the Tropospheric Monitoring Instrument (TROPOMI)) and an array of ground-based UV spectrometers (Network for Observation of Volcanic and Atmospheric Change (NOVAC)). Time-averaged lava discharge rates (TADRs) are obtained from two automatic satellite-based hot spot detection systems: MIROVA and MODVOLC. Assuming that the lava volumes measured in the field are accurate, the MIROVA system gave the best estimation of erupted volume among the methods investigated. We use a reverse petrological method to constrain pre-eruptive magmatic sulfur contents based on observed SO2 emissions and lava volumes. We also show that a direct petrological approach using SO2 data might be a viable alternative for TADR estimation during cloudy weather that compromises hot spot detection. In several eruptions we observed a terminal increase in TADR and SO2 emissions after initial emission of evolved degassed magma. We ascribe this to input of deeper, volatile-rich magma into the plumbing system towards the end of these eruptions. Furthermore, we find no evidence of volatile excess in the five eruptions studied, which were thus mostly fed by shallow degassed magma.

2016 ◽  
Author(s):  
Can Li ◽  
Nickolay A. Krotkov ◽  
Simon Carn ◽  
Yan Zhang ◽  
Robert J. D. Spurr ◽  
...  

Abstract. 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 pre-defined 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 (~ 1700 kt total SO2) and Sierra Negra in 2005 (> 1100 DU maximal 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 coarser spatial and spectral resolution of the Suomi National Polar-orbiting Partnership (Suomi-NPP) Ozone Mapping and Profiler Suite (OMPS) instrument, application of the new PCA algorithm to OMPS data produces highly consistent retrievals between OMI and OMPS. The new PCA algorithm is therefore capable of continuing the volcanic SO2 data record well into the future using current and future hyperspectral UV satellite instruments.


2017 ◽  
Vol 10 (2) ◽  
pp. 445-458 ◽  
Author(s):  
Can Li ◽  
Nickolay A. Krotkov ◽  
Simon Carn ◽  
Yan Zhang ◽  
Robert J. D. Spurr ◽  
...  

Abstract. 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 (∼ 1700 kt total SO2) and Sierra Negra in 2005 (> 1100 DU 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 coarser spatial and spectral resolution of the Suomi National Polar-orbiting Partnership (Suomi-NPP) Ozone Mapping and Profiler Suite (OMPS) instrument, application of the new PCA algorithm to OMPS data produces highly consistent retrievals between OMI and OMPS. The new PCA algorithm is therefore capable of continuing the volcanic SO2 data record well into the future using current and future hyperspectral UV satellite instruments.


2019 ◽  
Author(s):  
Zoe Y. W. Davis ◽  
Sabour Baray ◽  
Chris A. McLinden ◽  
Aida Khanbabakhani ◽  
William Fujs ◽  
...  

Abstract. Sarnia, ON experiences pollutant emissions disproportionate to its relatively small size. The small size of the city limits traditional top-down emission estimate techniques (e.g., satellite) but a low-cost solution for emission monitoring is Mobile-MAX-DOAS. Measurements were made using this technique from 21/03/2017 to 23/03/2017 along various driving routes to retrieve vertical column densities (VCDs) of NO2 and SO2 and to estimate emissions of NOx and SO2 from the Sarnia region. A novel aspect of the current study was the installation of a NOx analyzer in the vehicle to allow real time measurement and characterization of near-surface NOx/NO2 ratios across the urban plumes, allowing improved accuracy of NOx emission estimates. Confidence in the use of near-surface measured NOx/NO2 ratios for estimation of NOx emissions was increased by relatively well-mixed boundary layer conditions. These conditions were indicated by similar temporal trends in NO2 VCDs and mixing ratios when measurements were sufficiently distant from the sources. Leighton ratios within transported plumes indicated peroxy radicals were likely disturbing the NO-NO2-O3 photostationary state through VOC oxidation. The average lower limit emission estimate of NOx from Sarnia was 1.60 ± 0.34 tonnes hr−1 using local 10 m elevation wind-speed measurements. Our estimates were larger than the downscaled annual 2017 NPRI reported industrial emissions of 0.9 tonnes NOx hr−1. Our lower limit estimate of SO2 emissions from Sarnia was 1.81 ± 0.83 tonnes SO2 hr−1, equal within uncertainty to the 2017 NPRI downscaled value of 1.85 tonnes SO2 hr−1. Satellite-derived NO2 VCDs over Sarnia from the Ozone Monitoring Instrument (OMI) were lower than Mobile-MAX-DOAS VCDs, likely due to the large pixel size relative to the city’s size. The results of this study support the utility of the Mobile-MAX-DOAS method for estimating NOx and SO2 emissions in relatively small, highly industrialized regions especially when supplemented with mobile NOx measurements.


2020 ◽  
Vol 20 (9) ◽  
pp. 5591-5607 ◽  
Author(s):  
Vitali Fioletov ◽  
Chris A. McLinden ◽  
Debora Griffin ◽  
Nicolas Theys ◽  
Diego G. Loyola ◽  
...  

Abstract. The paper introduces the first TROPOMI-based sulfur dioxide (SO2) emissions estimates for point sources. A total of about 500 continuously emitting point sources releasing about 10 kt yr−1 to more than 2000 kt yr−1 of SO2, previously identified from Ozone Monitoring Instrument (OMI) observations, were analyzed using TROPOMI (TROPOspheric Monitoring Instrument) measurements for 1 full year from April 2018 to March 2019. The annual emissions from these sources were estimated and compared to similar estimates from OMI and Ozone Mapping Profiling Suite (OMPS) measurements. Note that emissions from many of these 500 sources have declined significantly since 2005, making their quantification more challenging. We were able to identify 274 sources where annual emissions are significant and can be reliably estimated from TROPOMI. The standard deviations of TROPOMI vertical column density data, about 1 Dobson unit (DU, where 1 DU =2.69×1016 molecules cm−2) over the tropics and 1.5 DU over high latitudes, are larger than those of OMI (0.6–1 DU) and OMPS (0.3–0.4 DU). Due to its very high spatial resolution, TROPOMI produces 12–20 times more observations over a certain area than OMI and 96 times more than OMPS. Despite higher uncertainties of individual TROPOMI observations, TROPOMI data averaged over a large area have roughly 2–3 times lower uncertainties compared to OMI and OMPS data. Similarly, TROPOMI annual emissions can be estimated with uncertainties that are 1.5–2 times lower than the uncertainties of annual emissions estimates from OMI. While there are area biases in TROPOMI data over some regions that have to be removed from emission calculations, the absolute magnitude of these are modest, typically within ±0.25 DU, which can be comparable with SO2 values over large sources.


2016 ◽  
Author(s):  
Verity J. B. Flower ◽  
Thomas Oommen ◽  
Simon A. Carn

Abstract. 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 the development of an automated volcanic plume detection method utilizing daily, global observations of sulphur 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 are analysed using a logistic regression analysis which permits the identification of volcanic events with an overall accuracy of over 80 %, and consistent plume identification when the volcanic plume SO2 loading exceeds ~ 400 tons. The accuracy and minimal user input requirements of the developed procedure provide a basis for the creation of an automated SO2 alert system providing volcanic alerts in regions where ground based volcano monitoring capabilities are limited. The technique could easily be adapted for use with satellite measurements of volcanic SO2 emissions from other platforms.


2016 ◽  
Author(s):  
Vitali E. Fioletov ◽  
Chris A. McLinden ◽  
Nickolay Krotkov ◽  
Can Li ◽  
Joanna Joiner ◽  
...  

Abstract. Sulphur 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 emissions 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.


2016 ◽  
Vol 16 (18) ◽  
pp. 11497-11519 ◽  
Author(s):  
Vitali E. Fioletov ◽  
Chris A. McLinden ◽  
Nickolay Krotkov ◽  
Can Li ◽  
Joanna Joiner ◽  
...  

Abstract. 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.


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