Radiative transfer corrections for accurate spectroscopic measurements of volcanic gas emissions

There is widespread use of passive remote sensing techniques to quantify trace gas column densities in volcanic plumes utilizing scattered sunlight as a light source. Examples include passive DOAS, COSPEC, and the SO₂ camera. In order to calculate trace gas concentrations or volcanic emission fluxes, knowledge about the optical path through the plume is necessary. In the past, a straight photon path through the plume has always been assumed although it was known that this is not always true. Here we present the results of model studies conducted specifically to quantify the effects of realistic radiative transfer in and around volcanic plumes on ground-based remote sensing measurements of SO₂. The results show that measurements conducted without additional information on average photon paths can be inaccurate under certain conditions, with possible errors spanning more than an order of magnitude. Both over and underestimation of the true column density can occur. Actual errors depend on parameters such as distance between instrument and plume, plume SO₂ concentration, plume aerosol load, as well as aerosol conditions in the ambient atmosphere. As an example, a measurement conducted with an SO₂ camera is discussed, the results of which can only be correctly interpreted if realistic radiative transfer is considered. Finally, a method is presented which for the first time allows the retrieval of actual average photon paths in spectroscopic (i.e. DOAS) measurements of adequate resolution. By allowing for a wavelength dependent column density during the evaluation of DOAS measurements, we show how radiative transfer effects can be corrected using information inherently available in the measured spectra, thus greatly enhancing the accuracy of DOAS measurements of volcanic emissions.     

Comparison of COSPEC and two miniature ultraviolet spectrometer systems for SO2 measurements using scattered sunlight

The correlation spectrometer (COSPEC), the principal tool for remote measurements of volcanic SO₂, is rapidly being replaced by low-cost, miniature, ultraviolet (UV) spectrometers. We compared two of these new systems with a COSPEC by measuring SO₂ column amounts at Kīlauea Volcano, Hawaii. The two systems, one calibrated using in-situ SO₂ cells, and the other using a calibrated laboratory reference spectrum, employ similar spectrometer hardware, but different foreoptics and spectral retrieval algorithms. Accuracy, signal-to-noise, retrieval parameters, and precision were investigated for the two configurations of new miniature spectrometer. Measurements included traverses beneath the plumes from the summit and east rift zone of Kīlauea, and testing with calibration cells of known SO₂ concentration. The results obtained from the different methods were consistent with each other, with <8% difference in estimated SO₂ column amounts up to 800 ppm m. A further comparison between the COSPEC and one of the miniature spectrometer configurations, the ‘FLYSPEC’, spans an eight month period and showed agreement of measured emission rates to within 10% for SO₂ column amounts up to 1,600 ppm m. The topic of measuring high SO₂ burdens accurately is addressed for the Kīlauea measurements. In comparing the foreoptics, retrieval methods, and resultant implications for data quality, we aim to consolidate the various experiences to date, and improve the application and development of miniature spectrometer systems.     

Rates of sulfur dioxide and particle emissions from White Island volcano,New Zealand,and an estimate of the total flux of major gaseous species

Airborne correlation spectrometry (COSPEC) was used to measure the rate of SO₂ emission at White Island on three dates, i.e., November 1983, 1230 ± 300 t/d; November 1984, 320 ± 120 t/d; and January 1985, 350 ± 150 t/d (t = metric tons). The lower emission rates are likely to reflect the long-term emission rates, whereas the November 1983 rate probably reflects conditions prior to the eruption of December 1983. The particle flux in the White Island plume, as determined with a quartz crystal microbalance/cascade in November 1983, was 1.3 t/d, unusually low for volcanic plumes. The observed plume particles, as shown from scanning electron microscopy, include halite, native sulfur, and silicates and are broadly similar to other volcanic plumes.Gas analyses from high-temperature volcanic fumaroles collected from June 1982 through November 1984 werde used together with the COSPEC data to estimate the flux of other gas species from White Island. The rates estimated are indicative of the long-term volcanic emission, i.e., 8000–9000 t/d H₂O, 900–1000 t/d CO₂, 70–80 t/d HCl, 1.5–2 t/d HF, and about 0.2 t/d NH₃. The long-term thermal power output at White Island is estimated at about 400 MW.     

SO2 emission of the 1974 eruption of Volcán Fuego,Guatemala

Volcán Fuego in the Central American Republic of Guatemala erupted violently in October, 1974. A remote sensing correlation spectrometer. COSPEC IV, which utilizes the characteristic molecular absorption of SO₂ in the ultraviolet was used to monitor the SO₂ content of the volcanic plume. Over a 60-day period measurements were made on 37 days between and following major eruptive phases. SO₂ emission rates corrected for atmospheric scattering of the spectral signal average 423 metric tons/day with a standard deviation of 252 metric tons/days. Late stage peaks in SO₂ emission at Fuego are consistent with the presence of anomalously high contents of soluble materials on the stratigraphically highest ashes from other Central American eruptions. Indications are that the SO₂ concentration within the volcanic plume increased as activity waned. These features imply that remote spectroscopic sensing of SO₂ and perhaps other gases in a volcanic plume may provide a relatively easy and inexpensive means of determining the cessation of violent eruptive activity.     

Imaging DOAS for volcanological applications

The simultaneous quantitative determination of two-dimensional bromine monoxide (BrO) and sulphur dioxide (SO₂) distributions in volcanic gas plumes is described. Measurements at the fumarolic field on the island Vulcano (autumn 2004) and in the plume of Mt. Etna volcano (spring 2005) were carried out with an Imaging DOAS instrument. The SO₂ fluxes of several fumaroles were estimated from two-dimensional distributions of SO₂. Additionally, the first two-dimensional distributions of BrO within a volcanic plume were successfully retrieved. Slant column densities of up to 2.6 × 10¹⁴ molecules per square centimetre were detected in the plume of Mt. Etna. The investigation of the BrO/SO₂ ratio, calculated from the two-dimensional distributions of SO₂ and BrO, shows an increase from the centre to the edge of the volcanic plume. These results have significance for the involvement of ozone during BrO formation processes in volcanic emissions.     

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

The emission rate of carbon dioxide escaping from the summit of Kīlauea Volcano, Hawai?i, 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 SO₂ emission 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.     

IDOAS: A new monitoring technique to study the 2D distribution of volcanic gas emissions

Imaging Differential Optical Absorption Spectroscopy (IDOAS) is an optical remote-sensing method using scattered sunlight as light source. It combines a “pushbroom” imaging spectrometer with the DOAS technique and thus allows imaging two-dimensional trace gas distributions, e.g., in volcanic plumes. The highly sensitive and specific detection of many trace gases simultaneously (specific molecules, not just elements, e.g. SO₂, BrO, NO₂, O₃, HCHO, etc.) is possible, and the temporal and spatial variation of these gases can be measured. The IDOAS system presented here enables the taking of two-dimensional images of trace gas distributions in a volcanic plume with a spatial resolution of 100 pixels horizontally × 64 pixels vertically, each with a field of view of 0.087° in horizontal and 0.208° in vertical directions. Therefore, IDOAS provides useful information about the chemical composition and chemical variability in a volcanic plume and allows studying plume dispersal and chemical transformations. The technique was applied to map the SO₂ distribution in the plume of Mt. Etna volcano for the first time in October 2003.     

A new technique to estimate volcanic gas composition: plume measurements with a portable multi-sensor system

A portable multi-sensor system was developed to measure volcanic plumes in order to estimate the chemical composition and temperature of volcanic gases. The multi-sensor system consists of a humidity–temperature sensor, SO₂ electrochemical sensor, CO₂ IR analyzer, pump and flow control units, pressure sensor, data logger, and batteries; the whole system is light (∼5 kg) and small enough to carry in a medium-size backpack. Volcanic plume is a mixture of atmosphere and volcanic gas; therefore volcanic gas composition and temperature can be estimated by subtracting the atmospheric gas background from the plume data. In order to obtain the contrasting data of the plume and the atmosphere, measurements were repeated in and out of the plume. The multi-sensor technique was applied to measure the plume of Tarumae, Tokachi, and Meakan volcanoes, Hokkaido, Japan. Repeated measurements at each volcano gave a consistent composition with ±10–30% errors, depending on the stability of the background atmospheric conditions. Fumarolic gas samples were also collected at the Tokachi volcano by a conventional method, and we found a good agreement (the difference <10%) between the composition estimated by the multi-sensor technique and conventional method. Those results demonstrated that concentration ratios of major volcanic gas species (i.e., H₂O, CO₂, and SO₂) and temperature can be estimated by the new technique without any complicated chemical analyses even for gases emitted from an inaccessible open vent. Estimation of a more detailed gas composition can be also achieved by the combination of alkaline filter techniques to measure Cl/F/S ratios in the plume and other sensors for H₂S and H₂.     

Evaluation of the Physical and Chemical Properties of Eyjafjallajökull Volcanic Plume Using a Cloud-Resolving Model

The Eyjafjallajökull volcanic eruption, which occurred on April 14, 2010, caused many environmental, air traffic and health problems. An attempt has been made to demonstrate for the first time that certain improvements could be made in the quantitative prediction of the volcanic ash parameters, and in the accounting of the processes in the immediate vicinity of the volcano, using a cloud-resolving model. This type of explicit modeling by treatment of volcanic ash and sulfate chemistry parameterization, with input of a number parameters describing the volcanic source, is the way forward for understanding the complex processes in plumes and in the future plume dispersion modeling. Results imply that the most significant microphysical processes are those related to accretion of cloud water, cloud ice and rainwater by snow, and accretion of rain and snow by hail. The dominant chemical conversion rates that give a great contribution to the sulfate budget are nucleation and dynamic scavenging and oxidation processes. A three-dimensional numerical experiment has shown a very realistic simulation of volcanic ash and other chemical compounds evolution, with a sloping structure strongly influenced by the meteorological conditions. In-cloud oxidation by H₂O₂ is the dominant pathway for SO₂ oxidation and allows sulfate to be produced within the SO₂ source region. The averaged cloud water pH of about 5.8 and rainwater pH of 4.5 over simulation time show quantitatively how the oxidation may strongly influence the sulfate budget and acidity of volcanic cloud. Compared to observations, model results are close in many aspects. Information on the near field volcanic plume behavior is essential for early preparedness and evacuation. This approach demonstrates a potential improvement in quantitative predictions regarding the volcanic plume distribution at different altitudes. It could be a useful tool for modeling volcanic plumes for better emergency measures planning.     

Estimation of SO<Subscript>2</Subscript> abundance in the eruption plume of Mt. Etna using two MIVIS thermal infrared channels: a case study from the Sicily-1997 Campaign

In this paper, an algorithm is developed based on the split-window technique, to estimate the SO₂ abundance in the plume of Mt. Etna volcano using the multispectral infrared and visible imaging spectrometer (MIVIS). The MIVIS data were remotely sensed in the thermal infrared (TIR) during the Sicily-1997 Campaign. In this study, the MODTRAN 3.5 code has been used to simulate the radiance at the sensor; the radiative transfer model was input along with the data of radio-sounding performed simultaneously with the MIVIS flight using a mobile radio-theodolite. From the SO₂ map, derived from the MIVIS image, the SO₂ flux along the axis of the plume was computed knowing the wind speed at the plume altitude. The SO₂ flux is variable along the plume axis. The average SO₂ flux (about 45 kg s^-1 on 12 June and about 30 kg s^-1 on 16 June) emitted from the vents is compared with the correlation spectrometer (COSPEC) measurements carried out by other teams (from the ground and from a light aircraft flying under the plume) during the MIVIS flight. Finally, by means of this algorithm it should be easier, with respect to the previously described procedure to monitor the SO₂ flux of a specific volcano such as Mt. Etna.     

Halogen oxide measurements at Masaya Volcano,Nicaragua using active long path differential optical absorption spectroscopy

Active Long Path Differential Optical Absorption Spectroscopy (LP-DOAS) measurements of halogen oxides were conducted at Masaya Volcano, in Nicaragua from April 14 to 26, 2007. The active LP-DOAS system allowed night-time halogen measurements and reduced the ClO detection limit by an order of magnitude when compared to previous passive DOAS measurements, as wavelengths below 300 nm could be used for the DOAS retrievals. BrO was detected with an average BrO/SO₂ molecular ratio of approximately 3 × 10⁻⁵ during the day. However, BrO values were below the detection limit of the instrument for all night-time measurements, a strong indication that BrO is not directly emitted, but rather the result of photochemical formation in the plume itself according to the autocatalytic “bromine explosion” mechanism. Despite the increased sensitivity, both ClO and OClO could not be detected. The achieved upper limits for the X/SO₂ ratios were 5 × 10⁻³ and 7 × 10⁻⁶, respectively. A rough calculation suggests that ClO and OClO should be present at similar abundances in volcanic plumes. Since the DOAS technique is orders of magnitude more sensitive for OClO than for ClO, this indicates that OClO should always be detectable in plumes in which ClO is found. However, further LP-DOAS studies are needed to conclusively clarify the role of chlorine oxides in volcanic plumes.     

Daily monitoring of Ecuadorian volcanic degassing from space

We present daily measurements of sulfur dioxide (SO₂) emissions from active volcanoes in Ecuador and southern Colombia between September 2004 and September 2006, derived from the Ozone Monitoring Instrument (OMI) on NASA's EOS/Aura satellite. OMI is an ultraviolet/visible spectrometer with an unprecedented combination of spatial and spectral resolution, and global coverage, that permits daily measurements of passive volcanic degassing from space. We use non-interactive processing methods to automatically extract daily SO₂ burdens and information on SO₂ sources from the OMI datastream. Maps of monthly average SO₂ vertical columns retrieved by OMI over Ecuador and S. Colombia are also used to illustrate variations in regional SO₂ loading and to pinpoint sources. The dense concentration of active volcanoes in Ecuador provides a stringent test of OMI's ability to distinguish SO₂ from multiple emitting sources. Our analysis reveals that Tungurahua, Reventador and Galeras were responsible for the bulk of the SO₂ emissions in the region in the timeframe of our study, with no significant SO₂ discharge detected from Sangay. At Galeras and Reventador, we conclude that OMI can detect variations in SO₂ release related to cycles of conduit sealing and degassing, which are a critical factor in hazard assessment. The OMI SO₂ data for Reventador are the most extensive sequence of degassing measurements available for this remote volcano, which dominated regional SO₂ production in June–August 2005. At Tungurahua, the OMI measurements span the waning stage of one eruptive cycle and the beginning of another, and we observe increasing SO₂ burdens in the months prior to explosive eruptions of the volcano in July and August 2006. Cumulative SO₂ loadings measured by OMI yield a total of ~ 1.16 Tg SO₂ emitted by volcanoes on mainland Ecuador/S. Colombia between September 2004 and September 2006; as much as 95% of this SO₂ may originate from non-eruptive degassing. Approximate apportionment of the total SO₂ loading indicates that ~ 40% originated from Tungurahua, with ~ 30% supplied by both Reventador and Galeras. These measurements of volcanic SO₂ degassing in Ecuador confirm OMI's potential as an effective, economical and risk-free tool for daily monitoring of SO₂ emissions from hazardous volcanoes.     

Contribution des Sondes Aérologiques Motorisées à l’Etude de la Physico-Chimie des Panaches Volcaniques

Our knowledge of the physico-chemical properties of volcanic plumes remains at an embryonic state, mainly because of the prohibitive cost of measurements made from aircraft, which alone can provide samples representative of the total aerosol and gaseous emission from a volcanic source. The authors show that a small Remotely Piloted Vehicle (R.P.V.), similar in design to the one they used for some probative flights over Mt. Etna, may be of great use in this field. They can, for instance, insure frequent measurement of the SO₂/HCl ratio in volcanic emanations close to active craters at times when the eruptive vents themselves cannot be sampled directly. In June 1978, we were thus able to measure a mean ratio of SO₂/HCl (7.6) in the Mt. Etna volcanic plume. In addition, a correlation spectrometer was in operation during the airborne sampling and allowed us to obtain order of magnitude values for the Mt. Etna discharge in water vapour (170000 tons/day), sulphur dioxide (1700 t/d), hydrochloric acid (340 t/d) and hydrofluoric acid (40 t/d). Widespread use of such R.P.V’s would insure the collection of a great deal of physicochemical data from volcanic plumes, data which are presently lacking and which could extensively enhance the efficiency of chemical methods of volcano surveillance.     

Real-time measurement of volcanic SO2 emissions: validation of a new UV correlation spectrometer (FLYSPEC)

A miniaturized, lightweight and low-cost UV correlation spectrometer, the FLYSPEC, has been developed as an alternative for the COSPEC, which has long been the mainstay for monitoring volcanic sulfur dioxide fluxes. Field experiments have been conducted with the FLYSPEC at diverse volcanic systems, including Masaya (Nicaragua), Poás (Costa Rica), Stromboli, Etna and Vulcano (Italy), Villarica (Chile) and Kilauea (USA). We present here those validation measurements that were made simultaneously with COSPEC at Kilauea between March 2002 and February 2003. These experiments, with source emission rates that ranged from 95 to 1,560 t d⁻¹, showed statistically identical results from both instruments. SO₂ path-concentrations ranged from 0 to >1,000 ppm-m with average correlation coefficients greater than r ²=0.946. The small size and low cost create the opportunity for FLYSPEC to be used in novel deployment modes that have the potential to revolutionize the manner in which volcanic and industrial monitoring is performed.     

Apparent downwind depletion of volcanic SO<Subscript>2</Subscript> flux—lessons from Masaya Volcano,Nicaragua

A series of 707 measurements at Masaya in 2005, 2006, and 2007 reveals that SO₂ emissions 15km downwind of the active vent appear to be ~33% to ~50% less than those measured only 5km from the vent. Measurements from this and previous studies indicate that dry deposition of sulfur from the plume and conversion of SO₂ to sulfate aerosols within the plume each may amount to a maximum of 10% loss, and are not sufficient to account for the larger apparent loss measured. However, the SO₂ measurement site 15km downwind is located on a ridge over which local trade winds, and the entrained plume, accelerate. Greater wind speeds cause localized dilution of the plume along the axis of propagation. The lower concentrations of SO₂ measured on the ridge therefore lead to calculations of lower fluxes when calculated at the same plume speed as measurements from only 5km downwind, and is responsible for the apparent loss of SO₂. Due to the importance of SO₂ emission rates with respect to hazard mitigation, petrologic studies, and sulfur budget calculations, measured fluxes of SO₂ must be as accurate as possible. Future campaigns to measure SO₂ flux at Masaya and similar volcanoes will require individual plume speed measurements to be taken at each flux measurement site to compensate for dilution and subsequent calculation of lower fluxes. This study highlights the importance of a comprehensive understanding of a volcano’s interaction with its surroundings, especially for low, boundary layer volcanoes.     

Mass Discharge in a Tracer Plume: Evaluation of the Theissen Polygon Method

A tracer plume was created within a thin aquifer by injection for 299 d of two adjacent “sub‐plumes” to represent one type of plume heterogeneity encountered in practice. The plume was monitored by snapshot sampling of transects of fully screened wells. The mass injection rate and total mass injected were known. Using all wells in each transect (0.77 m well spacing, 1.4 points/m² sampling density), the Theissen Polygon Method (TPM) yielded apparently accurate mass discharge (M_d) estimates at three transects for 12 snapshots. When applied to hypothetical sparser transects using subsets of the wells with average spacing and sampling density from 1.55 to 5.39 m and 0.70 to 0.20 points/m², respectively, the TPM accuracy depended on well spacing and location of the wells in the hypothesized transect with respect to the sub‐plumes. Potential error was relatively low when the well spacing was less than the widths of the sub‐plumes (>0.35 points/m²). Potential error increased for well spacing similar to or greater than the sub‐plume widths, or when less than 1% of the plume area was sampled. For low density sampling of laterally heterogeneous plumes, small changes in groundwater flow direction can lead to wide fluctuations in M_d estimates by the TPM. However, sampling conducted when flow is known or likely to be in a preferred direction can potentially allow more useful comparisons of M_d over multiyear time frames, such as required for performance evaluation of natural attenuation or engineered remediation systems.     

A reassessment of current volcanic emissions from the Central American arc with specific examples from Nicaragua

The Central American volcanic arc supplies a significant proportion of the persistent annual global sulphur dioxide emissions from volcanoes. In November/December 2003, we completed a survey of the arc section from Mombacho to San Cristóbal in Nicaragua recording individual mean fluxes of 800, 530 and 220 Mg day^− 1 in the plumes from San Cristóbal, Telica and Masaya, respectively. An assessment of fluxes published since 1997 along the entire Central America arc yields a mean total arc flux of SO₂ of 4360 Mg day^− 1 or 8–16% of the annual estimated global volcanic SO₂ flux to the troposphere. New field data shows that Masaya volcano continues to show stable HCl/SO₂ and HF/SO₂ ratios, suggesting a sustained flux of these components of ∼ 220 and 30 Mg day^− 1, respectively (1997 to 2004). Masaya's plume composition also appears to have been stable, between 2001 and 2003, with respect to all the particulate species measured, with significant fluxes of SO₄²⁻ (4 Mg day^− 1), Na⁺ (0.9–1.3 Mg day^− 1) and K⁺ (0.7 Mg day^− 1). Extrapolating the Masaya plume species ratios to the entire Central American arc gives mean HCl and HF fluxes of 1300 and 170 Mg day^− 1 and a particulate sulphate flux of 40 Mg day^− 1 for 1997 to 2004, although without further understanding of the degassing processes and sources at depth of these different volatiles, these arc-scale estimates should be treated with caution. Combining our arc scale mean SO₂ flux with published measurements of volcanic gas compositions with respect to CO₂ and H₂O allows us to estimate mean CO₂ fluxes of 4400–9600 Mg day^− 1 and H₂O fluxes of 70,000–78,000 Mg day^− 1 for the arc. Preliminary comparisons of these estimates of outgassing rates with published volatile input fluxes into the Central American subduction zone, suggest that Cl is more efficiently recycled through the subduction zone than CO₂. The results for H₂O are inconclusive.     

Automated,high time-resolution measurements of SO<Subscript>2</Subscript> flux at Soufrière Hills Volcano,Montserrat

We report here the first results from an automated, telemetered UV scanning spectrometer system for monitoring SO ₂ emission rates at Soufrière Hills Volcano, Montserrat. Two spectrometers receive light by way of a motor-driven stepping prism and telescope in order to make vertical scans of the volcanic plume. Spectral data from these spectrometers, situated 2,800 m apart and 4,500 m from the volcano, are relayed back to the observatory every 4–5 s via radio modems. A full scan of the plume is accomplished every 1–6 min by the (time-synchronised) spectrometers and a SO ₂ emission rate is calculated using the SO ₂ slant concentrations, scan angles and plume speeds estimated from the wind speed from a telemetered weather station near to the volcano. The plume's position and dimensions are calculated using the angular data from the two spectrometers. The plume height varies significantly diurnally and seasonally and is important in order to minimise the error on SO ₂ emission rates. The new scanning system (Scanspec) provides SO ₂ emission rates from 08:00 to 16:00 h local time every day. Preliminary results highlight a number of features of the SO ₂ time series and plume dynamics and give our first indications of the errors and limits of detection of this system. SO ₂ emission rates vary widely on all time scales (minutes, days, months). This new system has already provided the first real and consistent indication that SO ₂ emission rates vary on a minutes to hours basis, which can be correlated with volcanic activity (for example, rockfall and pyroclastic flow activity). It is anticipated that this system at Soufrière Hills will yield information on shallow processes occurring on short time scales (periods of minutes to hours) as well as deep processes relating to magma supply rates, which will be associated with longer wavelength SO ₂ signals of weeks to months.     

Tomographic reconstruction of gas plumes using scanning DOAS

This paper presents a method to reconstruct the gas distribution inside a vertical cross section of a gas plume by combining data from two or more scanning DOAS instruments using a tomographic algorithm. The method can be applied to gas plumes from any single, elevated point source, such as a volcano or industrial chimney. Such two-dimensional concentration distributions may prove to be useful for example in plume chemistry, dispersion and environmental impact studies. Here we show the case with one scanning DOAS instrument located on each side of the plume, which is the easiest and most economic setup as well as the most useful in routine monitoring of e.g. volcanic gas emissions. The paper investigates the conditions under which tomographic reconstructions can be performed and discusses limitations of this setup. The proposed method has been studied theoretically by numerical simulations and has been experimentally tested during two field campaigns, with measurements of SO₂ emissions from a volcano and a power plant. The simulations show that, under good measurement conditions, the algorithm presented performs well, which is further confirmed by the experimental results.     

Accurately measuring volcanic plume velocity with multiple UV spectrometers

A fundamental problem with all ground-based remotely sensed measurements of volcanic gas flux is the difficulty in accurately measuring the velocity of the gas plume. Since a representative wind speed and direction are used as proxies for the actual plume velocity, there can be considerable uncertainty in reported gas flux values. Here we present a method that uses at least two time-synchronized simultaneously recording UV spectrometers (FLYSPECs) placed a known distance apart. By analyzing the time varying structure of SO₂ concentration signals at each instrument, the plume velocity can accurately be determined. Experiments were conducted on Kīlauea (USA) and Masaya (Nicaragua) volcanoes in March and August 2003 at plume velocities between 1 and 10 m s⁻¹. Concurrent ground-based anemometer measurements differed from FLYSPEC-measured plume speeds by up to 320%. This multi-spectrometer method allows for the accurate remote measurement of plume velocity and can therefore greatly improve the precision of volcanic or industrial gas flux measurements. Editorial responsibility: A. Woods