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1.
A tripod-mounted correlation spectrometer was used to measure SO2 emissions from Pu`u `O`o vent, mid-ERZ, Kilauea, Hawaii between Episodes 33 and 34 (June 13 to July 6, 1985). In 24 repose days, 906 measurements were collected, averaging 38 determinations/day. Measurements reflect 13% of the total 576 hours of the repose and 42% of the bright daylight hours. The average SO2 emission for the 24-day repose interval is 167±83 t/d, a total of 4000 tonnes emitted for the entire repose. The large standard deviation reflects the puffing character of the plume. The overall rate of SO2 degassing gently decreased with a zero-intercept of 44–58 days and was interrupted by two positive peaks. The data are consistent with the gas emanating from a cylindrical conduit of 50 meter diameter and a length of 1700 meters which degasses about 50% of its SO2 during 24 days. This is in support of the Pu'u `O`o model of Greenland et al. (1987). 36 hours before the onset of Episode 34 (July 5–6, 1985), elevated SO2 emissions were detected while the magma column was extremely active ultimately spilling over during dome fountaining. A mid-repose anomaly of SO2 emission (June 21–22, 1985) occurs two days before a sudden increase in the rate of summit inflation (on June 24, 1985), suggesting magma was simultaneously being injected in both the ERZ and summit reservoir until July 24 when it was channelled only to the summit reservoir. This implies degassing magma is sensitive to perturbations within the rift zone conduit system and may at times reflect these disturbances. Periods of 7–45 min are detected in the daily SO2 emissions, which possibly reflect timing of convective overturn in the cylindrical magma body. If the 33–34 repose interval is considered representative of other repose periods, the ERZ reposes of Jan 1983–Jan 1986 ERZ activity, contributed 1.6 × 105 tonnes of SO2 to the atmosphere. Including summit fuming from non-eruptive fumaroles (2.7 × 105 tonnes SO2); 28% of the total SO2 budget from Kilauea between Jan 1983 to Jan 1986 was contributed by quiescent degassing, and the remainder was released during explosive fountaining episodes.  相似文献   

2.
Volcanic gas samples were collected from July to November 1985 from a lava pond in the main eruptive conduit of Pu'u O'o from a 2-week-long fissure eruption and from a minor flank eruption of Pu'u O'o. The molecular composition of these gases is consistent with thermodynamic equilibrium at a temperature slightly less than measured lava temperatures. Comparison of these samples with previous gas samples shows that the composition of volatiles in the magma has remained constant over the 3-year course of this episodic east rift eruption of Kilauea volcano. The uniformly carbon depleted nature of these gases is consistent with previous suggestions that all east rift eruptive magmas degas during prior storage in the shallow summit reservoir of Kilauea. Minor compositional variations within these gas collections are attributed to the kinetics of the magma degassing process.  相似文献   

3.
Popocatépetl volcano in central Mexico has been erupting explosively and effusively for almost 4 years. SO2 emission rates from this volcano have been the largest ever measured using a COSPEC. Pre-eruptive average SO2 emission rates (2–3 kt/d) were similar to the emission rates measured during the first part of the eruption (up to August 1995) in contrast with the effusive–explosive periods (March 1996–January 1998) during which SO2 emission rates were higher by a factor of four (9–13 kt/d). Based on a chronology of the eruption and the average SO2 emission rates per period, the total SO2 emissions (up to 1 January 1998) are estimated to be about 9 Mt, roughly half as much as the SO2 emissions from Mount Pinatubo in a shorter period. Popocatépetl volcano is thus considered as a high-emission rate, passively degassing eruptive volcano. SO2 emission rates and SO2 emissions are used here to make a mass balance of the erupted magma and related gases. Identified excess SO2 is explained in terms of continuous degassing of unerupted magma and magma mixing. Fluctuations in SO2 emission rate may be a result of convection and crystallization in the chamber or the conduits, cleaning and sealing of the plumbing system, and/or SO2 scrubbing by the hydrothermal system.  相似文献   

4.
 The 1963 eruption of Gunung Agung produced 0.95 km3 dense rock equivalent (DRE) of olivine±hornblende-bearing, weakly phyric, basaltic andesite tephra and lava. Evidence for magma mixing in the eruptive products includes whole-rock compatible and incompatible trace element trends, reverse and complex compositional zoning of mineral phases, disequilibrium mineral assemblages, sieve-textured plagioclase phenocrysts, and augite rims on reversely zoned orthopyroxene. Basalt magma mixed with pre-existing andesite magma shortly before eruption to yield basaltic andesite with a temperature of 1040–1100  °C at an assumed pressure of 2 kb, f O2>NNO, and an average melt volatile content (H2O±CO2) of 4.3 wt.%. Magma-mixing end members may have provided some of the S and Cl emitted in the eruption. Glass inclusions in phenocrysts contain an average of 650 ppm S and 3130 ppm Cl as compared with 70 ppm and 2220 ppm, respectively, in the matrix glass. Maximum S and Cl contents of glass inclusions approach 1800 and 5000 ppm, respectively. Application of the petrologic method to products of the 1963 eruption for estimating volatile release yields of 2.5×1012 g (Mt) of SO2 and 3.4 Mt of Cl released from the 0.65 km3 of juvenile tephra which contributed to stratospheric injection of H2SO4 aerosols on 17 March and 16 May, when eruption column heights exceeded 20 km above sea level. An independent estimate of SO2 release from atmospheric aerosol loading (11–12 Mt) suggests that approximately 7 Mt of SO2 was injected into the stratosphere. The difference between the two estimates can be most readily accounted for by the partitioning of S, as well as some Cl, from the magma into a water-rich vapor phase which was released upon eruption. For other recent high-S-release eruptions of more evolved and oxidized magmas (El Chichón, Pinatubo), the petrologic method gives values two orders of magnitude less than independent estimates of SO2 emissions. Results from this study of the Agung 1963 magma and its volatile emissions, and from related studies on eruptions of more mafic magmas, suggest that SO2 emissions from eruptions of higher-S-solubility magma may be more reliably estimated by the petrologic method than may those from more-evolved magma eruptions. Received: 29 June 1994 / Accepted: 25 April 1996  相似文献   

5.
Kilauea's 1955 eruption was the first major eruption (longer than 2 days) on its east rift zone in 115 years. It lasted 88 days during which 108 × 106 m3 of lava was erupted along a discontinuous, 15-km-long system of fissures. A wide compositional range of lavas was erupted including the most differentiated lavas (5.0 wt% MgO) from a historic Kilauea eruption. Lavas from the first half of the eruption are strongly differentiated (5.0–5.7 wt% MgO); later lavas are weakly to moderately differentiated (6.2–6.7 wt% MgO). Previous studies using only major-element compositions invoked either crystal fractionation (Macdonald and Eaton 1964) or magma mixing (Wright and Fiske 1971) as models to explain the wide compositional variation in the lavas. To further evaluate these models detailed petrographic, mineralogical, and whole-rock, major, and trace element XRF analyses were made of the 1955 lavas. Plagioclase and clinopyroxene in the early and late lavas show no petrographic evidence for magma mixing. Olivines from both the early and late lavas show minor resorption, which is typical of tholeiitic lavas with low MgO contents. Core-to-rim microprobe analyses across olivine, augite, and plagioclase mineral grains give no evidence of disequilibrium features related to mixing. Instead, plots of An/Ab vs distance from the core (D) and %Fo vs (D)4.5 generated essentially linear trends indicative of simple crystal fractionation. Least-squares, mass-balance calculations for major- and trace-element data using observed mineral compositions yield excellent results for crystal fractionation (sum of residuals squared <0.01 for major elements, and <5% for trace elements); magma mixing produced less satisfactory results especially for Cr. Furthermore, trace-element plots of Zr vs Sr, Cr, and A12O3 generate curved trends indicative of crystal fractionation processes. There is no evidence that mixing occurred in the 1955 lavas. Instead, the data are best explained by crystal fractionation involving a reservoir that extends at least 15 km along Kilauea's east rift zone. A dike was intruded into the rift zone from the summit reservoir eight days after the eruption started. Instead of causing magma mixing, the dike probably acted as a hydraulic plunger forcing more of the stored magma to be erupted.  相似文献   

6.
During the early part of a seismic swarm preceding eruption and caldera formation at Miyakejima Volcano, discoloured sea surfaces were observed 1.5 km off the western coast of Miyakejima on 27 June 2000. A later survey of the area using a multi-beam side scan sonar and a remotely operated small submarine revealed four craters of 20–30 m diameter aligned east-west in a 100×10–30 m area on the seafloor, with hot water at 140°C being released from one of the centres. Each crater consists of submarine spatter overlain in part by scoria lapilli. Dredged spatter from the craters was fresh, and there was no evidence of activity of marine organisms on the spatter surface, indicating that the discoloured sea surface resulted from magmatic eruption on the seafloor. This eruption occurred when a westward-propagating seismic swarm, initiated beneath Miyakejimas summit, passed through the area. Finding new magma on the seafloor demonstrates that this seismic swarm was associated with intruding magma, moving outward from beneath Miyakejima. Submarine spatter shows flattened shapes with a brittle crust formed by cooling in water, and its composition is aphyric andesite of 54 wt% SiO2. The spatter is similar in whole rock and mineral composition to spatter erupted in 1983. However, the wide range of Cl in melt inclusions in plagioclase of the 27 June submarine spatter shows that it is not simply a remnant of the 1983 magma, which has only high Cl melt inclusions in plagioclase. The mixed character of melt inclusions suggests involvement of a magma with low Cl melt inclusions. The magma erupted explosively on 18 August from Miyakejimas summit, considered as the second juvenile magma in this eruption, contains low Cl melt inclusions in plagioclase. Based on these observations and the eruption sequence, we present the following model: (1) A shallow magma chamber was filled with a remnant of 1983 magma that had evolved to a composition of 54–55 wt% SiO2. (2) Injection of the 18 August magma into this chamber generated a mixed magma having a wide range of Cl in melt inclusions contained plagioclase. The magma mixing might have occurred shortly before the submarine eruption and could have been a trigger for the initiation of the removal of magma from the chamber as an extensive dyke, which eventually led to caldera subsidence.Editorial responsibility: S Nakada, T Druitt  相似文献   

7.
A Landsat Thematic Mapper (TM) image acquired on 23 July 1991 recorded widespread activity associated with the Episode 48 of the Pu'u 'O'o-Kupaianaha eruption of Kilauea Volcano, Hawaii. The scene contains a very large number (>3500) of thermally elevated near infrared (0.8–2.35 m) pixels (each 900 m2), which enable the spatial distribution of volcanic activity to be identified. This activity includes a lava lake within Pu'u 'O'o cone, an active lava tube system (7.9 km in length) with skylights between the Kupaianaha lava shield and several ocean entry points, and extensive active surface flows (total area of 1.3 km2) within a much larger area of cooling flows (total16 km2). The production of an average flux density map from the TM data of the flow field, wherein the average flux density is defined in units of Wm-2, allows for the chronology of emplacement of active and cooling flows to be determined. The flux density map reveals that there were at least three breakouts (>5000 Wm-2) feeding active flows, but on the day that the data were collected the TM recorded a waning phase of surface activity in this area, based on the relatively large amount of intermediate power-emitting (cooling) flows compared to high power-emitting (active) flows. The production of a comparable flux density map for future eruptions would aid in the assessment of volcanic hazards if the data were available in near-real time.  相似文献   

8.
Chronology and products of the 2000 eruption of Miyakejima Volcano, Japan   总被引：1，自引：1，他引：0  
Lateral migration of magma away from Miyakejima volcanic island, Japan, generated summit subsidence, associated with summit explosions in the summer of 2000. An earthquake swarm beneath Miyakejima began on the evening of 26 June 2000, followed by a submarine eruption the next morning. Strong seismic activity continued under the sea from beneath the coast of Miyakejima to a few tens of kilometers northwest of the island. Summit eruptive event began with subsidence of the summit on 8 July and both explosions and subsidence continued intermittently through July and August. The most intense eruptive event occurred on 18 August and was vulcanian to subplinian in type. Ash lofted into the stratosphere fell over the entire island, and abundant volcanic bombs were erupted at this time. Another large explosion took place on 29 August. This generated a low-temperature pyroclastic surge, which covered a residential area on the northern coast of the island. The total volume of tephra erupted was 9.3×106 m3 (DRE), much smaller than the volume of the resulting caldera (6×108 m3). Migration of magma away from Miyakejima was associated with crustal extension northwest of Miyakejima and coincident shrinkage of Miyakejima Island itself during July–August 2000. This magma migration probably caused stoping of roof rock into the magma reservoir, generating subsurface cavities filled with hydrothermal fluid and/or magmatic foam and formation of a caldera (Oyama Caldera) at the summit. Interaction of hydrothermal fluid with ascending magma drove a series of phreatic to phreatomagmatic eruptions. It is likely that new magma was supplied to the reservoir from the bottom during waning stage of magmas migration, resulting in explosive discharge on 18 August. The 18 August event and phreatic explosions on 29 August produced a conduit system that allowed abundant SO2 emission (as high as 460 kg s–1) after the major eruptive events were over. At the time of writing, inhabitants of the island (about 3,000) have been evacuated from Miyakejima for more than 3 years.  相似文献   

9.
The Pu'u 'O'o-Kupaianaha eruption (1983-present) is the longest lived rift eruption of either Kilauea or neighboring Mauna Loa in recorded history. The initial fissure opening in January 1983 was followed by three years of episodic fire fountaining at the Pu'u 'O'o vent on Kilauea's east rift zone 19km from the summit (episodes 4–47). These spectacular events gave way in July 1986 to five and a half years of nearcontinuous, low-level effusion from the Kupaianaha vent, 3km to the cast (episode 48). A 49th episode began in November 1991 with the opening of a new fissure between Pu'u 'O'o and Kupaianaha. this three week long outburst heralded an era of more erratic eruptive behavior characterized by the shut down of Kupaianaha in February 1992 and subsequent intermittent eruption from vents on the west flank of Pu'u 'O'o (episodes 50 and 51). The events occurring over this period are due to progressive shrinkage of the rift-zone reservoir beneath the eruption site, and had limited impact on eruption temperatures and lava composition.  相似文献   

10.
A narrow band spectroradiometer was used to determine the characteristic temperatures of a very active channeled lava flow for the phase 50 eruption of Pu'u 'O'o on the East Rift Zone of Kilauea Volcano, Hawaii. During the twilight of 19 February 1992, 14 spectra of this activity were acquired over a 51 minute interval [18.29 to 19.20 Hawaiian Standard Time (HST)], from which the thermal distribution of energy of two 18 m2 areas, one near the center and one near the margin of the flow, may be investigated. A twocomponent thermal mixing model applied to the data taken of the center of the channel gave, in the most powerful instance (1.8x105 W/m2), a crust temperature of 940° C, a hot component temperature of 1120°C and a hot radiating area of 60% of the total area. A simultaneous spectrum acquired near the channeled flow margin yielded a crust temperature of 586° C and a hot area of only 1.2% of the total area radiating at 1130° C. Average radiant flux densities recorded for the center of the lava channel (1.3x105 W/m2 average) are much greater than previous measurements of lava lakes (4.9x103 W/m2) or recently emplaced lava flows (maximum of 7.2x104 W/m2). The energetic nature of this eruption is shown by satellite measurements made at 02.33 HST on 22 February 1992 by the Advanced Very High Resolution Radiometer in Band 2 (0.72–1.10 m). These show the utility of using existing satellites with moderate resolution (1 km x 1 km pixels) and high temporal coverage (eight overpasses each day for Hawaii) as potential thermal alarms for rapidly assessing the hazard potential of large volcanic eruptions.  相似文献   

11.
This paper presents the results of 7 years (Aug. 1999–Oct. 2006) of SO2 gas measurements during the ongoing eruption of Tungurahua volcano, Ecuador. From 2004 onwards, the operation of scanning spectrometers has furnished high temporal resolution measurements of SO2 flux, enabling this dataset to be correlated with other datasets, including seismicity. The emission rate of SO2 during this period ranges from less than 100 to 35,000 tonnes/day (t d− 1) with a mean daily emission rate of 1458 t d− 1 and a standard deviation of ± 2026 t d− 1. Average daily emissions during inferred explosive phases are about 1.75 times greater than during passive degassing intervals. The total amount of sulfur emitted since 1999 is estimated as at least 1.91 Mt, mostly injected into the troposphere and carried westwards from the volcano. Our observations suggest that the rate of passive degassing at Tungurahua requires SO2 exsolution of an andesitic magma volume that is two orders of magnitude larger than expected for the amount of erupted magma. Two possible, and not mutually exclusive, mechanisms are considered here to explain this excess degassing: gas flow through a permeable stagnant-magma-filled conduit and gas escape from convective magma overturning in the conduit. We have found that real-time gas monitoring contributes significantly to better eruption forecasting at Tungurahua, because it has provided improved understanding of underlying physical mechanisms of magma ascent and eruption.  相似文献   

12.
Among the series of eruptions at Miyakejima volcano in 2000, the largest summit explosion occurred on 18 August 2000. During this explosion, vesiculated bombs and lapilli having cauliflower-like shapes were ejected as essential products. Petrological observation and chemical analyses of the essential ejecta and melt inclusions were carried out in order to investigate magma ascent and eruption processes. SEM images indicate that the essential bombs and lapilli have similar textures, which have many tiny bubbles, crystal-rich and glass-poor groundmass and microphenocrysts of plagioclase, augite and olivine. Black ash particles, which compose 40% of the air-fall ash from the explosion, also have similar textures to the essential bombs. Whole-rock analyses show that the chemical composition of all essential ejecta is basaltic (SiO2=51–52 wt%). Chemical analyses of melt inclusions in plagioclase and olivine phenocrysts indicate that melt in the magma had 0.9–1.9 wt% H2O, <0.011 wt% CO2, 0.04–0.17 wt% S and 0.06–0.1 wt% Cl. The variation in volatile content suggests degassing of the magma during ascent up to a depth of about 1 km. The ratio of H2O and S content of melt inclusions is similar to that of volcanic gas, which has been intensely and continuously emitted from the summit since the end of August 2000, indicating that the 18 August magma is the source of the gas emission. Based on the volatile content of the melt inclusions and the volcanic gas composition, the initial bulk volatile content of the magma was estimated to be 1.6–1.9 wt% H2O, 0.08–0.1 wt% CO2, 0.11–0.17 wt% S and 0.06–0.07 wt% Cl. The basaltic magma ascended from a deeper chamber (10 km) due to decrease in magma density caused by volatile exsolution with pressure decrease. The highly vesiculated magma, which had at least 30 vol% bubbles, may have come into contact with ground water at sea level causing the large explosion of 18 August 2000.Editorial responsibility: S. Nakada, T. DuittAn erratum to this article can be found at  相似文献   

13.
Mount Cameroon (4,095 m high and with a volume of ~1,200 km3) is one of the most active volcanoes in Africa, having erupted seven times in the last 100 years. This stratovolcano of basanite and hawaiite lavas has an elliptical shape, with over a hundred cones around its flanks and summit region aligned parallel to its NE--SW-trending long axis. The 1999 (28 March–22 April) eruption was restricted to two sites: ~2,650 m (site 1) and ~1,500 m (site 2). Similarly, in the eruption in 2000 (28 May–19 June), activity occurred at two sites: ~4,095 m (site 1) and ~3,300 m (site 2). During both eruptions, the higher vents were more explosive, with strombolian activity, while the lower vents were more effusive. Accordingly, most of the lava (~8×107 m3 in 1999 and ~6×106 m3 in 2000) was emitted from the lower sites. The 1999–2000 lavas are predominantly basanites with low Ni (5–79 ppm), Cr (40–161 ppm) and mg numbers (34–40). Olivine (Fo77–85, phenocrysts and Fo68–72, microlites), clinopyroxene (Wo47En41Fs10 to Wo51En34Fs15), plagioclase (An49–67) and titanomagnetite are the principal phenocryst and groundmass phases. The lavas contain xenocrysts of olivine and clinopyroxene, which are interpreted as fragments of intrusive rocks disrupted by magma ascent. Major and trace element characteristics point to early fractionation of olivine. The clinopyroxenes (Al2O3 1.36–7.83 wt%) have high Aliv/Alvi ratios (1.3–1.8) and are rich in TiO2, characteristics typical of low pressure clinopyroxenes. Geochemical differences between the 1999–2000 lavas and those from previous eruptions, such as higher Nb/Zr of the former, suggest that different eruptions discharged magmas that evolved differently in space and time. Geophysical and petrological data indicate that these fractionated magmas originated just below the geophysical Moho (at 20–22 km) in the lithospheric mantle. During ascent, the magmas disrupted intrusions and earlier magma pockets. The main ascent path is below the summit, where newly arrived magma degasses. Degassed magma simultaneously intrudes the flank rift zones where most lava is extruded.An erratum to this article can be found at  相似文献   

14.
Sr and Nd isotope and geochemical investigations were performed on a remarkably homogeneous, high-silica rhyolite magma reservoir of the Aira pyroclastic eruption (22,000 years ago), southern Kyushu, Japan. The Aira caldera was formed by this eruption with four flow units (Osumi pumice fall, Tsumaya pryoclastic flow, Kamewarizaka breccia and Ito pyroclastic flow). Quite narrow chemical compositions (e.g., 74.0–76.5 wt% of SiO2) and Sr and Nd isotopic values (87Sr/86Sr=0.70584–0.70599 and Nd=−5.62 to −4.10) were detected for silicic pumices from the four units, with the exception of minor amounts of dark pumices in the units. The high Sr isotope ratios (0.7065–0.7076) for the dark pumices clearly suggest a different origin from the silicic pumices. Andesite to basalt lavas in pre-caldera (0.37–0.93 Ma) and post-caldera (historical) eruptions show lower 87Sr/86Sr (0.70465–0.70540) and higher Nd (−1.03 to +0.96) values than those of the Aira silicic and dark pumices. Both andesites of pre- and post-caldera stages are very similar in major- and trace-element characteristics and isotope ratios, suggesting that the both andesites had a same source and experienced the same process of magma generation (magma mixing between basaltic and dacitic magmas). Elemental and isotopic signatures deny direct genetic relationships between the Aira pumices and pre- and post-caldera lavas. Relatively upper levels of crust (middle–upper crust) are assumed to have been involved for magma generation for the Aira silicic and dark pumices. The Aira silicic magma was derived by partial melting of a separate crust which had homogeneous chemistry and limited isotope compositions, while the magma for the Aira dark pumice was generated by AFC mixing process between the basement sedimentary rocks and basaltic parental magma, or by partial melting of crustal materials which underlay the basement sediments. The silicic magma did not occupy an upper part of a large magma body with strong compositional zonation, but formed an independent magma body within the crust. The input and mixing of the magma for dark pumices to the base of the Aira silicic magma reservoir might trigger the eruptions in the upper part of the magma body and could produce a slight Sr isotope gradient in the reservoir. An extremely high thermal structure within the crust, which was caused by the uprise and accumulation of the basaltic magma, is presumed to have formed the large volume of silicic magma of the Aira stage.  相似文献   

15.
Magma plumbing system of the 2000 eruption of Miyakejima Volcano, Japan   总被引：1，自引：0，他引：1  
During the 2000 eruption at Miyakejima Volcano, two magmas with different compositions erupted successively from different craters. Magma erupted as spatter from the submarine craters on 27 June is aphyric basaltic andesite (<5 vol% phenocrysts, 51.4–52.2 wt% SiO2), whereas magma issued as volcanic bombs from the summit caldera on 18 August is plagioclase-phyric basalt (20 vol% phenocrysts, 50.8–51.3 wt% SiO2). The submarine spatter contains two types of crystal-clots, A-type and A-type (andesitic type). The phenocryst assemblages (plagioclase, pyroxenes and magnetite) and compositions of clinopyroxene in these clots are nearly the same, but only A-type clots contain Ca-poor plagioclase (An < 70). We consider that the A-type clots could have crystallized from a more differentiated andesitic magma than the A-type clots, because FeO*/MgO is not strongly influenced during shallow andesitic differentiation. The summit bombs contain only B-type (basaltic type) crystal-clots of Ca-rich plagioclase, olivine and clinopyroxene. The A-type and B-type clots have often coexisted in Miyakejima lavas of the period 1469–1983, suggesting that the magma storage system consists of independent batches of andesitic and basaltic magmas. According to the temporal variations of mineral compositions in crystal-clots, the andesitic magma became less evolved, and the basaltic magma more evolved, over the past 500 years. We conclude that gradually differentiating basaltic magma has been repeatedly injected into the shallower andesitic magma over this period, causing the andesitic magma to become less evolved with time. The mineral chemistries in crystal-clots of the submarine spatter and 18 August summit bombs of the 2000 eruption fall on the evolution trends of the A-type and B-type clots respectively, suggesting that the shallow andesitic and deeper basaltic magmas existing since 1469 had successively erupted from different craters. The 2000 summit collapse occurred due to drainage of the andesitic magma from the shallower chamber; as the collapse occurred, it may have caused disruption of crustal cumulates which then contaminated the ascending, deeper basalt. Thus, porphyritic basaltic magma could erupt alone without mixing with the andesitic magma from the summit caldera. The historical magma plumbing system of Miyakejima was probably destroyed during the 2000 eruption, and a new one may now form.Editorial responsibility: S Nakada, T Druitt  相似文献   

16.
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   

17.
After the March–April 1986 explosive eruption a comprehensive gas study at Augustine was undertaken in the summers of 1986 and 1987. Airborne COSPEC measurements indicate that passive SO2 emission rates declined exponentially during this period from 380±45 metric tons/day (T/D) on 7/24/86 to 27±6 T/D on 8/24/87. These data are consistent with the hypothesis that the Augustine magma reservoir has become more degassed as volcanic activity decreased after the spring 1986 eruption. Gas samples collected in 1987 from an 870°C fumarole on the andesitic lava dome show various degrees of disequilibrium due to oxidation of reduced gas species and condensation (and loss) of H2O in the intake tube of the sampling apparatus. Thermochemical restoration of the data permits removal of these effects to infer an equilibrium composition of the gases. Although not conclusive, this restoration is consistent with the idea that the gases were in equilibrium at 870°C with an oxygen fugacity near the Ni–NiO buffer. These restored gas compositions show that, relative to other convergent plate volcanoes, the Augustine gases are very HCl rich (5.3–6.0 mol% HCl), S rich (7.1 mol% total S), and H2O poor (83.9–84.8 mol% H2O). Values of D and 18O suggest that the H2O in the dome gases is a mixture of primary magmatic water (PMW) and local seawater. Part of the Cl in the Augustine volcanic gases probably comes from this shallow seawater source. Additional Cl may come from subducted oceanic crust because data by Johnston (1978) show that Cl-rich glass inclusions in olivine crystals contain hornblende, which is evidence for a deep source (>25km) for part of the Cl. Gas samples collected in 1986 from 390°–642°C fumaroles on a ramp surrounding the inner summit crater have been oxidized so severely that restoration to an equilibrium composition is not possible. H and O isotope data suggest that these gases are variable mixtures of seawater, FMW, and meteoric steam. These samples are much more H2O-rich (92%–97% H2O) than the dome gases, possibly due to a larger meteoric steam component. The 1986 samples also have higher Cl/S, S/C, and F/Cl ratios, which imply that the magmatic component in these gases is from the more degassed 1976 magma. Thus, the 1987 samples from the lava dome are better indicators than the 1986 samples of degassing within the Augustine magma reservoir, even though they were collected a year later and contain a significant seawater component. Future gas studies at Augustine should emphasize fumaroles on active lava domes. Condensates collected from the same lava-dome fumarole have enrichments ot 107–102 in Cl, Br, F, B, Cd, As, S, Bi, Pb, Sb, Mo, Zn, Cu, K, Li, Na, Si, and Ni. Lower-temperature (200°–650°C) fumaroles around the volcano are generally less enriched in highly volatile elements. However, these lower-termperature fumaroles have higher concentration of rock-forming elements, probably derived from the wall rock.  相似文献   

18.
The petrology of the highly phyric two-pyroxene andesitic to dacitic pyroclastic rocks of the November 13, 1985 eruption of Nevado del Ruiz, Colombia, reveals evidence of: (1) increasingly fractionated bulk compositions with time; (2) tapping of a small magma chamber marginally zoned in regard to H2O contents (1 to 4%), temperature (960–1090°C), and amount of residual melt (35 to 65%); (3) partial melting and assimilation of degassed zones in the hotter less dense interior of the magma chamber; (4) probable heating, thermal disruption and mineralogic and compositional contamination of the magma body by basaltic magma “underplating”; and (5) crustal contamination of the magmas during ascent and within the magma chamber. Near-crater fall-back or “spill-over” emitted in the middle of the eruptive sequence produced a small pyroclastic flow that became welded in its central and basal portions because of ponding and thus heat conservation on the flat glaciated summit near the Arenas crater. The heterogeneity of Ruiz magmas may be related to the comparatively small volume (0.03 km3) of the eruption, nearly ten times less than the 0.2 km3 of the Plinian phase of Mount St. Helens, and probable steep thermal and PH2O gradients of a small source magma chamber, estimated at 300 m long and 100 m wide for an assumed ellipsoidal shape.  相似文献   

19.
K lauea Volcano, Hawai‘i, currently hosts the longest running SO2 emission-rate data set on the planet, starting with initial surveys done in 1975 by Stoiber and his colleagues. The 17.5-year record of summit emissions, starting in 1979, shows the effects of summit and east rift eruptive processes, which define seven distinctly different periods of SO2 release. Summit emissions jumped nearly 40% with the onset (3 January 1983) of the Pu‘u ‘ ‘ -K paianaha eruption on the east rift zone (ERZ). Summit SO2 emissions from K lauea showed a strong positive correlation with short-period, shallow, caldera events, rather than with long-period seismicity as in more silicious systems. This correlation suggests a maturation process in the summit magma-transport system from 1986 through 1993. During a steady-state throughput-equilibrium interval of the summit magma reservoir, integration of summit-caldera and ERZ SO2 emissions reveals an undegassed volume rate of effusion of 2.1×105 m3/d. This value corroborates the volume-rate determined by geophysical methods, demonstrating that, for K lauea, SO2 emission rates can be used to monitor effusion rate, supporting and supplementing other, more established geophysical methods. For the 17.5 years of continuous emission rate records at K lauea, the volcano has released 9.7×106 t (metric tonnes) of SO2, 1.7×106 t from the summit and 8.0×106 t from the east rift zone. On an annual basis, the average SO2 release from K lauea is 4.6×105 t/y, compared to the global annual volcanic emission rate of 1.2×107 t/y.  相似文献   

20.
The eruption that started in the Hekla volcano in South Iceland on 17 January 1991, and came to an end on 11 March, produced mainly andesitic lava. This lava covers 23 km2 and has an estimated volume of 0.15 km3. This is the third eruption in only 20 years, whereas the average repose period since 1104 is 55 years. Earthquakes, as well as a strain pulse recorded by borehole strainmeters, occurred less than half an hour before the start of the eruption. The initial plinian phase was very short-lived, producing a total of only 0.02 km3 of tephra. The eruption cloud attained 11.5 km in height in only 10 min, but it became detached from the volcano a few hours later. Several fissures were active during the first day of the eruption, including a part of the summit fissure. By the second day, however, the activity was already essentially limited to that segment of the principal fissure where the main crater subsequently formed. The average effusion rate during the first two days of the eruption was about 800 m3 s–1. After this peak, the effusion rate declined rapidly to 10–20 m3 s–1, then more slowly to 1 m3 s–1, and remained at 1–12 m3 s–1 until the end of the eruption. Site observations near the main crater suggest that the intensity of the volcanic tremor varied directly with the force of the eruption. A notable rise in the fluorine concentration of riverwater in the vicinity of the eruptive fissures occurred on the 5th day of the eruption, but it levelled off on the 6th day and then remained essentially constant. The volume and initial silica content of the lava and tephra, the explosivity and effusion rate during the earliest stage of the eruption, as well as the magnitude attained by the associated earthquakes, support earlier suggestions that these parameters are positively related to the length of the preceeding repose period. The chemical difference between the eruptive material of Hekla itself and the lavas erupted in its vicinity can be explained in terms of a density-stratified magma reservoir located at the bottom of the crust. We propose that the shape of this reservoir, its location at the west margin of a propagating rift, and its association with a crustal weakness, all contribute to the high eruption frequency of Hekla.  相似文献   

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