首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
Data from a series of laboratory experiments show the relationships between measured correlation spectrometer (COSPEC) sulfur-dioxide (SO2) burdens, automatic gain control (AGC) deflections, and visible wavelength opacities in ash-laden plumes. The data show that the COSPEC reliably measures (within a 10% accuracy) SO2 burdens up to AGC deflections of 2 V and visible wavelength opacities of 50%. Beyond these limits, the under measurement of the SO2 burden is not well constrained. During typical COSPEC runs, these limits are rarely violated. The 10% error introduced by measuring ash-laden plumes is acceptable because the error is small relative to other error sources associated with the technique, especially plume velocity; and the error is correctable which allows for a wider range of plume conditions to be measured.These results imply that the densest SO2 concentrations near the volcanic source can be measured. This is important so that SO2 is not lost from the volcanic plume due to physical and chemical processes and that measurements are conducted under maximum signal to noise ratios.  相似文献   

2.
An SO2 flux of 1170±400 (1) tonnes per day was measured with a correlation spectrometer (COSPEC) in October and November 1986 from the continuous, nonfountaining, basaltic East Rift Zone eruption (episode 48A) of Kilauea volcano. This flux is 5–27 times less than those of highfountaining episodes, 3–5 times greater than those of contemporaneous summit emissions or interphase Pu'u O'o emissions, and 1.3–2 times the emissions from Pu'u O'o alone during 48A. Calculations based on the SO2 emission rate resulted in a magma supply rate of 0.44 million m3 per day and a 0.042 wt% sulfur loss from the magma upon eruption. Both of these calculated parameters agree with determinations made previously by other methods.  相似文献   

3.
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.  相似文献   

4.
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.  相似文献   

5.
To investigate the isotopic composition and age of water in volcanic gases and magmas, we analyzed samples from 11 active volcanoes ranging in composition from tholeiitic basalt to rhyolite: Mount St. Helens (USA), Kilauea (USA), Pacaya (Guatemala), Galeras (Colombia), Satsuma Iwo-Jima (Japan), Sierra Negra and Alcedo (Ecuador), Vulcano (Italy), Parícutin (Mexico), Kudryavy (Russia), and White Island (New Zealand). Tritium at relatively low levels (0.1–5 T.U.) is found in most emissions from high-temperature volcanic fumaroles sampled, even at discharge temperatures >700°C. Although magmatic fluids sampled from these emissions usually contain high CO2, Stotal, HCl, HF, B, Br, 3He R/RA, and low contents of air components, stable isotope and tritium relations of nearly all such fluids show mixing of magmatic volatiles with relatively young meteoric water (model ages≤75 y). Linear δD/δ18O and 3H/δ18O mixing trends of these two end-members are invariably detected at arc volcanoes. Tritium is also detected in fumarole condensates at hot spot basalt volcanoes, but collecting samples approaching the composition of end-member magmatic fluid is exceedingly difficult. In situ production of 3H, mostly from spontaneous fission of 238U in magmas is calculated to be <0.001 T.U., except for the most evolved compositions (high U, Th, and Li and low H2O contents). These values are below the detection limit of 3H by conventional analytical techniques (about 0.01 T.U. at best). We found no conclusive evidence that natural fusion in the Earth produces anomalous amounts of detectable 3H (>0.05 T.U.).  相似文献   

6.
Use of eddy covariance (EC) techniques to map the spatial distribution of diffuse volcanic CO2 fluxes and quantify CO2 emission rate was tested at the Horseshoe Lake tree-kill area on Mammoth Mountain, California, USA. EC measurements of CO2 flux were made during September–October 2010 and ranged from 85 to 1,766 g m−2 day−1. Comparative maps of soil CO2 flux were simulated and CO2 emission rates estimated from three accumulation chamber (AC) CO2 flux surveys. Least-squares inversion of measured eddy covariance CO2 fluxes and corresponding modeled source weight functions recovered 58–77% of the CO2 emission rates estimated based on simulated AC soil CO2 fluxes. Spatial distributions of modeled surface CO2 fluxes based on EC and AC observations showed moderate to good correspondence (R 2 = 0.36 to 0.70). Results provide a framework for automated monitoring of volcanic CO2 emissions over relatively large areas.  相似文献   

7.
Helium isotopic ratios ranging from 20 to 32 times the atmospheric 3He/4He(RA) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the 3He/4He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower 3He/4He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 RA), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium.Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low 3He/4He) helium.3He/4He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in 3He/4He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 RA) helium with some (variable) component of lithospheric contamination added during “breakthrough”, while the later stages are characterized by a relaxation toward lithospheric 3He/4He ratios (～ 8 RA) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in 3He/4He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume.  相似文献   

8.
We analyse shortwave infrared thermal data of the phase 1 eruption of Unzen Volcano (Japan) extracted from eight nighttime Thematic Mapper (TM) images taken from the Landsat 5 satellite between October 1991 and November 1992. We identify two discrete regions of the dome that were heated to high temperature by the ongoing eruptive activity; a fumarolically heated region and an area associated with the effusion of new lava. We concentrate analysis on the fumarolically heated region and investigate the relationships between parameters derived from the infrared radiance data and the nature of the fumarolic gas and magma fluxes. Temporal variations in the parameters derived from the radiance data closely follow those observed in the measured rate of magma effusion. The positive correlation observed between the fumarolically driven shortwave infrared flux and the magma discharge rate (r2=0.64) indicates that degassing occurred efficiently and in proportion to the amount of magma supplied. Over our monitoring period, the data suggest that gas accumulation within the edifice did not occur, this conclusion agreeing with a previous finding obtained using correlation spectrometer (COSPEC) analysis of SO2 flux rates. A positive correlation (r2=0.56) was also found between the mean radiance of the pixels in the fumarolically heated region and the overall size of that region. This suggests a potential mechanism whereby, when gas pressure within the edifice increased, excess gas escaped through additional pathways to the surface as well through an increased flux at the main fumarolic vents.  相似文献   

9.
We measured SO2 emission rate from six volcanoes in Latin America (Santa Ana, El Salvador; San Cristóbal and Masaya, Nicaragua; Arenal and Poás, Costa Rica; Tungurahua and Sierra Negra, Ecuador) and from Mt. Etna, Italy, using two different remote sensing techniques: COSPEC (COrrelation SPECtrometer) and miniDOAS (miniaturized Differential Optical Absorption Spectroscopy). One of the goals of this study was to evaluate the differences in SO2 emission rates obtained by these two methods. The observed average SO2 emission rates measured during this study were 2688 t·d−1 from Tungurahua in July 2006, 2375 t·d−1 in September 2005 and 480 t·d−1 in February 2006 from Santa Ana, 1200 t·d−1 in May 2005 from Etna, 955 t·d−1 in March 2006 and 1165 t·d−1 in December 2006 from Masaya, 5400 t·d−1 of March 7, 2006 and 265 t·d−1 in March 2006 from San Cristobal, 113 t·d−1 in April 2006 from Arenal, 104 t·d−1 in April 2006 from Poás and 11 t·d−1 in July 2006 from Sierra Negra volcano. Most of the observed relative differences of SO2 emission measurements from COSPEC and miniDOAS were lower than 10%.  相似文献   

10.
Airborne and ground-based (correlation spectrometer, cascade impactor, and photoelectric counter together with intake filter probes) measurements are described for the volcanic emissions from Popocatépetl volcano (Mexico) from December 23, 1994 to January 28, 1995. Measurements of SO2 restarted 48 h after the eruption onset of December 21, 1994. Maximum sulfur dioxide (4560 t d−1) plus 3.8×104 t d−1 of particulate matter were ejected on December 24, 1994. The maximum rate of ejection occurred coincidentally with the maximum amplitude of harmonic tremor and the maximum number of seismic type B events. Sulfur dioxide emission rates ranged from 1790 to 2070 t d−1 (December 23–24, 1994). Afterwards, sulfur dioxide emission rates clearly indicated a consistent decline. However, frequent gas and ash emission puffs exhibited SO2 fluxes reaching values as high as 3060 t d−1. The emission SO2 baseline for the period of study (February 1994–January 1995) was about 1000 t d−1. Ejection velocity of particulate matter was approximately 270 m s−1 reaching a height of about 2.5 km over the summit. The immediate aerosol dispersion area was estimated at 6.0×104 km2 maximum. The microscopic structure of particles (aerosol and tephra) showed a fragile material, probably coming from weathered crustal layers. X-ray fluorescence and neutron-activation analysis from the impactor samples found the following elements: Si, Al, Ca, S, P, Cl, K, Ni, Fe, Ti, Sc, Cu, Zn, Mn, Sr, Cr, Co, Y, Br, Se, Ga, Rb, Hg and Pb. Morphological analysis shows that ash samples might be from pulverized basaltic rock indicating that the Popocatépetl eruption of December 21, 1994 was at low temperature. The microscopic structure of puff material showed substance aggregates consisted of fragile rock, water and adsorbed SO2. These aggregates were observed within water droplets of approximately 1 mm and even larger. Sulfur transformations in the droplets occurred intensively. Volcanic ash contained 5–6% of sulfur during the first expulsion hours. Elemental relative concentrations with respect to Al show that both Si and S have relative concentrations >1, i.e., 13.73 and 2.17, respectively in agreement with the photoelectric counter and COSPEC measurements.  相似文献   

11.
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.  相似文献   

12.
The chemical composition and D/H, and ratios have been determined for the acid hot waters and volcanic gases discharging from Zaō volcano in Japan. The thermal springs in Zaō volcano issue acid sulfate-chloride type waters (Zaō) and acid sulfate type waters (Kamoshika). Gases emitted at Kamoshika fumaroles are rich in CO2, SO2 and N2, exclusive of H2O. Chloride concentrations and oxygen isotope data indicate that the Zaō thermal waters issue a fluid mixture from an acid thermal reservoir and meteoric waters from shallow aquifers. The waters in the Zaō volcanic system have slight isotopic shifts from the respective local meteoric values. The isotopic evidence indicates that most of the water in the system is meteoric in origin. Sulfates in Zaō acid sulfate-chloride waters with δ34S values of around +15‰, are enriched in 34S compared to Zaō H2S, while the acid sulfate waters at Kamoshika contain supergene light sulfate (δ34S = + 4‰) derived from volcanic sulfur dioxide from the volcanic exhalations. The sulfur species in Zaō acid waters are lighter in δ34S than those of other volcanic areas, reflecting the difference in total pressure.  相似文献   

13.
The enrichment of some metals (Al, Mg, Na, K, Cu, Zn, Cd) in volcanic gases is measured by an emanation coefficient εx relating the amount of the element x in lavas and in aerosols.εx is determined in the volcanic emissions of Mount Etna (Sicily), with regard to that of210Pb. The accuracy of the results is limited by the geochemical behavior of common lead compared to that of210Pb. Concerning the most volatile species, it appears that practically all the volcanic aerosols are produced by evaporation followed by gas-to-particle conversion and the spattered fraction appears to be negligible.  相似文献   

14.
Condensate samples were collected in 1992 from a high-temperature (300° C) fumarole on the floor of the Halemaumau Pit Crater at Kilauea. The emergence about two years earlier of such a hot fumarole was unprecedented at such a central location at Kilauea. The condensates have hydrogen and oxygen isotopic compositions which indicate that the waters emitted by the fumarole are composed largely of meteoric water, that any magmatic water component must be minor, and that the precipitation that was the original source to the fumarole fell on a recharge area on the slopes of Mauna Loa Volcano to the west. However, the fumarole has no tritium, indicating that it taps a source of water that has been isolated from atmospheric water for at least 40 years. It is noteworthy, considering the unstable tectonic environment and abundant local rainfall of the Kilauea and Mauna Loa regions, that waters which are sources to the hot fumarole remain uncontaminated from atmospheric sources over such long times and long transport distances. As for the common, boiling point fumaroles of the Kilauea summit region, their 18O, D and tritium concentrations indicate that they are dominated by recycling of present day meteoric water. Though the waters of both hot and boiling point fumaroles have dominantly meteoric sources, they seem to be from separate hydrological regimes. Large concentrations of halogens and sulfur species in the condensates, together with the location at the center of the Kilauea summit region and the high temperature, initially suggested that much of the total mass of the emissions of the hot fumarole, including the H2O, might have come directly from a magma body. The results of the present study indicate that it is unreliable to infer a magmatic origin of volcanic waters based solely on halogen or sulfur contents, or other aspects of chemical composition of total condensates.  相似文献   

15.
The results from two different types of gas measurement, telemetered in situ monitoring of reducing gases on the dome and airborne measurements of sulfur dioxide emission rates in the plume by correlation spectrometry, suggest that the combination of these two methods is particularly effective in detecting periods of enhanced degassing that intermittently punctuate the normal background leakage of gaseous effluent from Mount St Helens to the atmosphere. Gas events were recorded before lava extrusion for each of the four dome-building episodes at Mount St Helens since mid-1984. For two of the episodes, precursory reducing gas peaks were detected, whereas during three of the episodes, COSPEC measurements recorded precursory degassing of sulfur dioxide. During one episode (October 1986), both reducing gas monitoring and SO2 emission rate measurements simultaneously detected a large gas release several hours before lava extrusion. Had both types of gas measurements been operational during each of the dome-building episodes, it is thought that both would have recorded precursory signals for all four episodes. Evidence from the data presented herein suggests that increased degassing at Mount St Helens becomes detectable when fresh upward-moving magma is between 2 km and a few hundred meters below the base of the dome and between about 60 and 12 hours before the surface extrusion of lava.  相似文献   

16.
Computer-simulation models of scoria cone degradation   总被引：2，自引：0，他引：2  
Long-term erosional modifications of the relatively simple morphology of scoria (‘cinder') cones are ideally suited for study by field and computer-simulation methods. A series of temporally-distinct cones in the San Francisco and Springerville volcanic fields of Arizona provides the foundation for documenting the degradational evolution of scoria cones in a semi-arid climate. Progressive changes due to erosion are illustrated by the systematic decrease with increasing age of various morphometric parameters, including scoria cone height, cone height/width ratio (Hco/Wco), crater depth/width ratio, and slope angle. For example, Holocene–latest Pleistocene cones in the San Francisco field have a mean Hco/Wco value of 0.178±0.041, a mean maximum slope angle of 29.7±4.2°, and a mean average slope angle of 26.4±7.3°, whereas the group of Pliocene cones have values of 0.077±0.024, 20.5±5.8°, and 8.7±2.7°, respectively. Comparative morphology of scoria cones is a potentially useful dating tool for mapping volcanic fields.In order to better understand the degradational modifications of these volcanic landforms, we have developed a numerical approach to simulate the surficial processes responsible for the erosion of a typical scoria cone. The simulation algorithm can apply either a linear diffusion-equation model or a model with a nonlinear transport law. Using a finite-difference formulation, the simulation operates upon a three-dimensional scoria cone input as a matrix of elevation values. Utilizing both field and model results, the correlation between changing Hco/Wco value, cone age, and computer time step was expressed graphically to derive comprehensive values of the transport or diffusion coefficient (Df) for both volcanic fields. For the San Francisco volcanic field, Df had a calculated value of 21.4 m2/kyr for the linear model and 5.3 m/kyr for the nonlinear model, while for the Springerville volcanic field Df had a calculated value of 24.4 m2/kyr for the linear model and 6.3 m/kyr for the nonlinear model.  相似文献   

17.
The variations in sulfur dioxide (SO2) emission from the Summit Craters of Mt. Etna were determined, with particular reference to the period 1993–1995. Vehicle-based weekly measurements of SO2 flux, using a correlation spectrometer (COSPEC), suggest new input of magma into the main feeder system of the volcano between 1993 and 1995. Minimal flux values (<1000 t/day) preceded the two eruptive events in the period 1987–1995. Only approximately 9.5% of the magma that contributed the SO2 emission was erupted during the same period. Received: 3 November 1997 / Accepted: 21 September 1998  相似文献   

18.
Our understanding on how ash particles in volcanic plumes react with coexisting gases and aerosols is still rudimentary, despite the importance of these reactions in influencing the chemistry and dynamics of a plume. In this study, six samples of fine ash (<100 m) from different volcanoes were measured for their specific surface area, as, porosity and water adsorption properties with the aim to provide insights into the capacity of silicate ash particles to react with gases, including water vapour. To do so, we performed high-resolution nitrogen and water vapour adsorption/desorption experiments at 77 K and 303 K, respectively. The nitrogen data indicated as values in the range 1.1–2.1 m2/g, except in one case where a as of 10 m2/g was measured. This high value is attributed to incorporation of hydrothermal phases, such as clay minerals, in the ash surface composition. The data also revealed that the ash samples are essentially non-porous, or have a porosity dominated by macropores with widths >500 Å. All the specimens had similar pore size distributions, with a small peak centered around 50 Å. These findings suggest that fine ash particles have relatively undifferentiated surface textures, irrespective of the chemical composition and eruption type. Adsorption isotherms for water vapour revealed that the capacity of the ash samples for water adsorption is systematically larger than predicted from the nitrogen adsorption as values. Enhanced reactivity of the ash surface towards water may result from (i) hydration of bulk ash constituents; (ii) hydration of surface compounds; and/or (iii) hydroxylation of the surface of the ash. The later mechanism may lead to irreversible retention of water. Based on these experiments, we predict that volcanic ash is covered by a complete monolayer of water under ambient atmospheric conditions. In addition, capillary condensation within ash pores should allow for deposition of condensed water on to ash particles before water reaches saturation in the plume. The total mass of water vapour retained by 1 g of fine ash at 0.95 relative water vapour pressure is calculated to be ~10–2 g. Some volcanic implications of this study are discussed.Editorial responsibility: J. Gilbert  相似文献   

19.
A field gas chromatograph, built in 1978, was used in the field to directly analyse volcanic gases before water vapor condensation. Tested in Vulcano (Italy), Kilauea (Hawaii) and Merapi (Indonesia), this field measurement technique provides the actual composition of the volcanic gas mixture. The technique avoids the depletion of sulfur gases and the dissolution of the acid gases in the condensed water during the cooling. Thus the mixture of H2S and SO2 in fumarolic and high temperature gases (up to 819°C) in equilibrium at the emission temperature was examined.  相似文献   

20.
The Yixian Formation at Sihetun in western Liao- ning Province has attracted considerable attention over the last two decades due to discovery of a wide range of well-preserved ‘feathered’ dinosaurs and primitive bird fossils[1―4]. This formation is dominated by vol- canic rocks, with fossil-bearing lacustrine sedimentary rocks at the upper part of the section[4]. The sedimen- tary rocks contain thin layers of tuff. According to previous studies[4], the total thickness of the Yixian Form…  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号