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1.
Hydrothermal activity is common in the Tatun Volcano Group of northern Taiwan. Helium isotopic compositions of fumarolic samples show that mantle component occupies more than 60% in the previous study. Along with recent seismic results, a magma reservoir is inferred to have existed beneath the area of Da-you-keng, where fumarolic venting is the most active in Tatun Volcano Group. Progressive increases of HCl concentrations and SO2/H2S ratio in fumaroles from Da-you-keng have been observed since August 2004. The HCl concentration changed from almost the detection limit to thousands of ppm, even up to 30,000 ppm. SO2/H2S ratios varied from almost 0 to 3; hence SO2 became the dominated S species in this area. These variations were accompanied by rising temperature of fumaroles in the Tatun Volcano Group, especially in the area of Da-you-keng (from boiling point to 131 °C). Meanwhile, 3He/4He ratios showed a decreasing trend but returned to normal values shortly thereafter. We propose two possible processes, 1) new magma supply and 2) recent opening of fractures in local area, to explain these observations. Based on the change of 3He/4He ratio and lack of ground deformation, we consider the latter might be more plausible.  相似文献   

2.
We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640 ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H2, and mildly enriched in CH4 and H2S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water–rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or 40?Ar/4?He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300 °C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO2 flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO2 fluxes across all the thermal/altered area suggests that 410 ± 140 t d− 1 CO2 are emitted at HSB (vent emissions not included). Diffuse fluxes of H2S were measured in Yellowstone for the first time and likely exceed 2.4 t d− 1 at HSB. Comparing estimates of the total estimated diffuse H2S emission to the amount of sulfur as SO42− in streams indicates ~ 50% of the original H2S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140–370 MW using CO2 as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1–3% for CO2, 2–8% for heat) of that estimated for the entire Yellowstone system.  相似文献   

3.
The edifice of Mount Rainier, an active stratovolcano, has episodically collapsed leading to major debris flows. The largest debris flows are related to argillically altered rock which leave areas of the edifice prone to failure. The argillic alteration results from the neutralization of acidic magmatic gases that condense in a meteoric water hydrothermal system fed by the melting of a thick mantle of glacial ice. Two craters atop a 2000-year-old cone on the summit of the volcano contain the world's largest volcanic ice-cave system. In the spring of 1997 two active fumaroles (T=62°C) in the caves were sampled for stable isotopic, gas, and geochemical studies.Stable isotope data on fumarole condensates show significant excess deuterium with calculated δD and δ18O values (−234 and −33.2‰, respectively) for the vapor that are consistent with an origin as secondary steam from a shallow water table which has been heated by underlying magmatic–hydrothermal steam. Between 1982 and 1997, δD of the fumarole vapor may have decreased by 30‰.The compositions of fumarole gases vary in time and space but typically consist of air components slightly modified by their solubilities in water and additions of CO2 and CH4. The elevated CO2 contents (δ13CCO2=−11.8±0.7‰), with spikes of over 10,000 ppm, require the episodic addition of magmatic components into the underlying hydrothermal system. Although only traces of H2S were detected in the fumaroles, most notably in a sample which had an air δ13CCO2 signature (−8.8‰), incrustations around a dormant vent containing small amounts of acid sulfate minerals (natroalunite, minamiite, and woodhouseite) indicate higher H2S (or possibly SO2) concentrations in past fumarolic gases.Condensate samples from fumaroles are very dilute, slightly acidic, and enriched in elements observed in the much higher temperature fumaroles at Mount St. Helens (K and Na up to the ppm level; metals such as Al, Pb, Zn Fe and Mn up to the ppb level and volatiles such as Cl, S, and F up to the ppb level).The data indicate that the hydrothermal system in the edifice at Mount Rainier consists of meteoric water reservoirs, which receive gas and steam from an underlying magmatic system. At present the magmatic system is largely flooded by the meteoric water system. However, magmatic components have episodically vented at the surface as witnessed by the mineralogy of incrustations around inactive vents and gas compositions in the active fumaroles. The composition of fumarole gases during magmatic degassing is distinct and, if sustained, could be lethal. The extent to which hydrothermal alteration is currently occurring at depth, and its possible influence on future edifice collapse, may be determined with the aid of on site analyses of fumarole gases and seismic monitoring in the ice caves.  相似文献   

4.
We observed a phytoplankton bloom downstream of a large estuarine plume induced by heavy precipitation during a cruise conducted in the Pearl River estuary and the northern South China Sea in May–June 2001. The plume delivered a significant amount of nutrients into the estuary and the adjacent coastal region, and enhanced stratification stimulating a phytoplankton bloom in the region near and offshore of Hong Kong. A several fold increase (0.2–1.8 μg Chl L−1) in biomass (Chl a) was observed during the bloom. During the bloom event, the surface water phytoplankton community structure significantly shifted from a pico-phytoplankton dominated community to one dominated by micro-phytoplankton (>20 μm). In addition to increased Chl a, we observed a significant drawdown of pCO2, biological uptake of dissolved inorganic carbon (DIC) and an associated enhancement of dissolved oxygen and pH, demonstrating enhanced photosynthesis during the bloom. During the bloom, we estimated a net DIC drawdown of 100–150 μmol kg−1 and a TAlk increase of 0–50 μmol kg−1. The mean sea–air CO2 flux at the peak of the bloom was estimated to be as high as ∼−18 mmol m−2 d−1. For an average surface water depth of 5 m, a very high apparent biological CO2 consumption rate of 70–110 mmol m−2 d−1 was estimated. This value is 2–6 times higher than the estimated air–sea exchange rate.  相似文献   

5.
The 3-d coupled physical–biogeochemical model ECOHAM (version 3) was applied to the Northwest-European Shelf (47°41′–63°53′N, 15°5′W–13°55′E) for the years 1993–1996. Carbon fluxes were calculated for the years 1995 and 1996 for the inner shelf region, the North Sea (511,725 km2). This period was chosen because it corresponds to a shift from a very high winter-time North Atlantic Oscillation Index (NAOI) in 1994/1995, to an extremely low one in 1995/1996, with consequences for the North Sea physics and biogeochemistry. During the first half of 1996, the observed mean SST was about 1 °C lower than in 1995; in the southern part of the North Sea the difference was even larger (up to 3 °C). Due to a different wind regime, the normally prevailing anti-clockwise circulation, as found in winter 1995, was replaced by more complicated circulation patterns in winter 1996. Decreased precipitation over the drainage area of the continental rivers led to a reduction in the total (inorganic and organic) riverine carbon load to the North Sea from 476 Gmol C yr−1 in 1995 to 340 Gmol C yr−1 in 1996. In addition, the North Sea took up 503 Gmol C yr−1 of CO2 from the atmosphere. According to our calculations, the North Sea was a sink for atmospheric CO2, at a rate of 0.98 mol C m−2 yr−1, for both years. The North Sea is divided into two sub-systems: the shallow southern North Sea (SNS; 190,765 km2) and the deeper northern North Sea (NNS; 320,960 km2). According to our findings the SNS is a net-autotrophic system (net ecosystem production NEP>0) but released CO2 to the atmosphere: 159 Gmol C yr−1 in 1995 and 59 Gmol C yr−1 in 1996. There, the temperature-driven release of CO2 outcompetes the biological CO2 drawdown. In the NNS, where respiratory processes prevail (NEP<0), 662 and 562 Gmol C yr−1 were taken up from the atmosphere in 1995 and 1996, respectively. Stratification separates the productive, upper layer from the deeper layers of the water column where respiration/remineralization takes place. Duration and stability of the stratification are determined by the meteorological conditions, in relation to the NAO. Our results suggest that this mechanism controlling the nutrient supply to the upper layer in the northern and central North Sea has a larger impact on the carbon fluxes than changes in lateral transport due to NAOI variations. The North Sea as a whole imports organic carbon and exports inorganic carbon across the outer boundaries, and was found to be net-heterotrophic, more markedly in 1996 than in 1995.  相似文献   

6.
This paper describes a methodology for the monitoring of fumarole temperatures at medium ranges (~ 6 km) using a handheld infrared camera (wavelength range: 8–13.5 µm). As a relationship between fumarole temperatures, gas flux and volcanic activity has been demonstrated by a number of studies, fumarole temperature data has a potential use as a monitoring tool. Volcán de Colima is an andesitic stratovolcano with a 300 m diameter summit crater formed by the destruction of the 2004 lava dome by a series of explosions in 2005. Between January 2006 and August 2007, sequences of thermal images were recorded from a viewpoint 6 km to the north during regular 24–48 hour monitoring excursions. The temperatures of fumaroles on the crater rim and the ground surface on the volcano's flanks were measured. A methodology was developed to remove data affected by clouds or volcanic water vapour based on rates of temperature change and scatter within the data. For the remaining data, it is demonstrated mathematically that at this range, typical variations in atmospheric transmissivity will affect the apparent temperatures by +/− 2 °C, while a 25% change in fumarole heat flux would change it by 5–10 °C. The mean night-time apparent temperature of the fumaroles was calculated for each excursion and showed an irregular decline over the 19 month period. Subtracting the radiant heat flux of flank rocks from those of the fumaroles removes seasonal variations and gives the clearest view of trends in the fumarole heat flux. A sharp drop in fumarole temperature during February 2007 coincided with the emergence of a lava dome in the crater. The declining fumarole temperature is interpreted to reflect decreasing gas flux from the crater in line with a change in eruptive regime from frequent, small, ash-rich explosions to slow effusion of lava.  相似文献   

7.
Partial pressure of CO2 in equilibrium with sample water (pCO2) for the coastal water in the Chukchi Sea was continuously observed in summer, 2008. Average daily CO2 flux calculated from the pCO2 and gas transfer coefficients ranged from −0.144 to −0.0701 g C m−2 day−1 depending on which gas transfer coefficient was used. The pCO2 before the landfast ice sheets melted appeared to be highly biologically controlled based on the following information: (1) the diurnal pattern of pCO2 was strongly correlated with Photosynthetic Photon Flux Density (PPFD); (2) high chlorophyll density was observed during periods of peak uptake; and (3) the day-to-day variation in the pCO2 strongly correlated with the presence or absence of near-shore ice sheets. The lowest pCO2 of 35 ppm together with the highest PPFD of 1362 μmol E m−2 s−1 were observed in the afternoon on June 28 in the presence of sea ice. The very low pCO2 observed in late June was likely caused by high photosynthetic rates related to high phytoplankton densities typically observed from spring to early summer near the ice edge, and by water low in salinity and CO2 released by melting sea ice early in the season.  相似文献   

8.
Physical, chemical and isotopic parameters were measured in fumaroles at the Vulcano crater and in drowned fumaroles near the beach. The data were used to define boundary conditions for possible conceptual models of the system.Crater fumaroles: time variations of CO2 and SO2 concentrations indicate mixing of saline gas-rich water with local fresh water. Cl/Br ratios of 300– 400 favour sea-water as a major source for Cl, Brand part of the water in the fumaroles. Cl concentrations and D values revealed, independently, amixing of 0.75 sea-water with 0.25 local freshwaterin furmarole F-5 during September 1982.Patterns of parameter correlation and mass balances reveal that CO2, S, NH3 and B originate from sources other than sea water. The CO2 value of 13C = – 2%o favours, at least partial, origin from decomposition of sedimentary rocks rather than mantle-derived material. Radiogenic4He(1.3 × lO–3 ccSTP/g water) and radiogenic40Ar(10.6 × 10–4 ccSTP/g water) are observed, (4He/40Ar)radiogenic = 1.2, well in the range of values observed in geothermal systems.Drowned fumaroles: strongly bubbling gas at a pond and at the beachappears to have the same origin and initial compositionas the crater fumaroles (2 km away). The fumarolic gas is modified by depletion of the reactive gases, caused by dissolution in shallow-water. Atmospheric Ne, Ar, Kr and Xe are addeden route, some radiogenic He and Ar are maintained. The Vulcano system seems to be strongly influenced by the contribution of sea-water and decomposition of sedimentary rocks. Evidence of magmatic contributions is mainly derived from heat.  相似文献   

9.
Anomalously high levels of mercury in sediment in the Lenga estuary, Chile are comparable to the most contaminated sites previously reported elsewhere. Total mercury (Hgtotal) concentrations range from 0.5 to 129 mg kg−1 and organic mercury (Hgorg) from 11 to 53 μg kg−1. The highest levels are in areas near the previous wastewater outfall of a chlo-alkali plant. The results show that the proportion of Hgorg/Hgtotal in the sediment varies by more than two orders of magnitude (0.02–5.7%) according to the concentration of Hgtotal. No correlation between the concentration of Hgorg and Hgtotal was found. The lack of correlation does contrast with the findings of other authors in culture media. Our results indicate that even at very high concentrations of Hgtotal and organic matter do not influence organic mercury formation in estuary sediments. The disparity in Hgtotal and Hgorg concentrations also attests to environmental differences in the formation.  相似文献   

10.
We report the first detailed study of spatial variations on the diffuse emission of carbon dioxide (CO2) and hydrogen sulfide (H2S) from Hengill volcanic system, Iceland. Soil CO2 and H2S efflux measurements were performed at 752 sampling sites and ranged from nondetectable to 17,666 and 722?g?m?2?day?1, respectively. The soil temperature was measured at each sampling site and used to evaluate the heat flow. The chemical composition of soil gases sampled at selected sampling sites during this study shows they result from a mixing process between deep volcanic/hydrothermal component and air. Most of the diffuse CO2 degassing is observed close to areas where active thermal manifestations occur, northeast flank of the Hengill central volcano close to the Nesjavellir power plant, suggesting a diffuse degassing structure with a SSW?CNNE trend, overlapping main fissure zone and indicating a structural control of the degassing process. On the other hand, H2S efflux values are in general very low or negligible along the study area, except those observed at the northeast flank of the Hengill central volcano, where anomalously high CO2 efflux and soil temperatures were also measured. The total diffuse CO2 emission estimated for this volcanic system was about 1,526?±?160?t?day?1 of which 453?t?day?1 (29.7?%) are of volcanic/hydrothermal origin. To calculate the steam discharge associated with the volcanic/hydrothermal CO2 output, we used the average H2O/CO2 mass ratio from 12 fumarole samples equal to 88.6 (range, 9.4?C240.2) as a representative value of the H2O/CO2 mass ratios for Hengill fumarole steam. The resulting estimate of the steam flow associated with the gas flux is equal to 40,154?t?day?1. The condensation of this steam results in thermal energy release for Helgill volcanic system of 1.07?×?1014?J?day?1 or to a total heat flow of 1,237?MWt.  相似文献   

11.
We estimated the net annual air–sea exchange of carbon dioxide (CO2) using monitoring data from the East Gotland Sea, Bornholm Sea, and Kattegat for the 1993–2009 period. Wind speed and the sea surface partial pressure of CO2 (pCO2w), calculated from pH, total alkalinity, temperature, and salinity, were used for the flux calculations. We demonstrate that regions in the central Baltic Sea and the Kattegat alternate between being sinks (−) and sources (+) of CO2 within the −4.2 to +5.2 mol m−2 yr−1 range. On average, for the 1994–2008 period, the East Gotland Sea was a source of CO2 (1.64 mol m−2 yr−1), the Bornholm Sea was a source (2.34 mol m−2 yr−1), and the Kattegat was a sink (−1.16 mol m−2 yr−1). Large inter-annual and regional variations in the air–sea balance were observed. We used two parameterizations for the gas transfer velocity (k) and the choice varied the air–sea exchange by a factor of two. Inter-annual variations in pCO2w between summers were controlled by the maximum concentration of phosphate in winter. Inter-annual variations in the CO2 flux and gas transfer velocity were larger between winters than between summers. This indicates that the inter-annual variability in the total flux was controlled by winter conditions. The large differences between the central Baltic Sea and Kattegat were considered to depend partly on the differences in the mixed layer depth.  相似文献   

12.
Detailed geochemistry supported by geologic mapping has been used to investigate Sulphur Springs, an acid-sulfate hot spring system that issues from the western flank of the resurgent dome inside Valles Caldera. The most intense activity occurs at the intersection of faults offsetting caldera-fill deposits and post-caldera rhyolites. Three geothermal wells in the area have encountered pressures <1 MPa and temperatures of 200°C at depths of 600 to 1000 m. Hot spring and fumarole fluids may discharge at boiling temperatures with pH 1.0 and SO4 8000 mg/l. These conditions cause argillic alterations throughout a large area.Non-condensible gases consist of roughly 99% CO2 with minor amounts of H2S, H2, and CH4. Empirical gas geothermometry suggests a deep reservoir temperature of 215 to 280°C. Comparison of 13C and 18O between CaCO3 from well cuttings and CO2 from fumarole steam indicates a fractionation temperature between 200 and 300°C by decarbonation of hydrothermally altered Paleozoic limestone and vein calcite in the reservoir rocks. Tritium concentrations obtained from steam condensed in a mudpot and deep reservoir fluids (Baca #13, 278°C) are 2.1 and 1.0 T.U. respectively, suggesting the steam originates from a reservoir whose water is mostly >50 yrs old. Deuterium contents of fumarole steam, deep reservoir fluid, and local meteoric water are practically identical even though 18O contents range through 4‰, thus, precipitation on the resurgent dome of the caldera could recharge the hydrothermal system by slow percolation. From analysis of D and 18O values between fumarol steam and deep reservoir fluid, steam reaches the surface either (1) by vaporizing relatively shallow groundwater at 200°C or (2) by means of a two-stage boiling process through an intermediate level reservoir at roughly 200°C.Although many characteristics of known vapor-dominated geothermal systems are found at Sulphur Springs, fundamental differences exist in temperature and pressure of our postulated vapor-zone. We propose that the reservoir beneath Sulphur Springs is too small or too poorly confined to sustain a “true” vapor-dominated system and that the Sulphur Springs system may be a “dying” vapor-dominated system that has practically boiled itself dry.  相似文献   

13.
The southern Yellow Sea (SYS), located to the north of the East China Sea (ECS), was considered part of the ECS when Tsunogai et al. (1999) proposed the “continental shelf pump” (CSP) hypothesis. However, the original CSP carbon dioxide (CO2) uptake flux (2.9 mol C m−2 yr−1) appears to have been overestimated, primarily due to the differences between the SYS and the ECS in terms of their CO2 system. In this paper, we estimated air-sea CO2 fluxes in the SYS using the surface water partial pressure of CO2 (pCO2) measured in winter, spring, and summer, as well as that estimated in fall via the relationship of pCO2 with salinity, temperature, and chlorophyll a. The results indicate that overall, the entire investigated area was a net source of atmospheric CO2 during summer, winter, and fall, whereas it was a net sink during spring. Spatially, the nearshore area was almost a permanent CO2 source, while the central SYS shifted from being a CO2 sink in spring to a source in the other seasons of the year. Overall, the SYS is a net source of atmospheric CO2 on an annual scale, releasing ∼7.38 Tg C (1 Tg=1012 g) to the atmosphere annually. Thus, the updated CO2 uptake flux in the combined SYS and ECS is reduced to ∼0.86 mol C m−2 yr−1. If this value is extrapolated globally following Tsunogai et al. (1999), the global continental shelf would be a sink of ∼0.29 Pg C yr−1, instead of 1 Pg C yr−1 (1 Pg=1015 g).The SYS as a net annual source of atmospheric CO2 is in sharp contrast to most mid- and high-latitude continental shelves, which are CO2 sinks. We argue that unlike the ECS and the North Sea where carbon on the shelf could be exported to the open ocean, the SYS lacks the physical conditions required by the CSP to transport carbon off the shelf effectively. The global validity of the CSP theory is thus questionable.  相似文献   

14.
Oldoinyo Lengai is the world's only active carbonatite volcano and considerable debate still surrounds the genesis of its magmas. Gases were collected from two fumaroles discharging close to the then active vent in October 2003. Measured fumarole temperatures were ≤ 195°C, despite the nearby, vigorous eruptive activity. Gases were sampled and analysed for noble gas isotopes. Freshly erupted natrocarbonatite lavas, a 1917 nephelinite and a sub-recent wollastonite bearing rock were also collected and analysed for noble gas isotopes using vacuum crushing techniques. In all the lava samples the neon, argon, krypton and xenon isotope ratio data are indistinguishable from air implying atmospheric contamination of the hygroscopic rocks. In the fumaroles, measured 3He/4He ratios are between 4 and 7 R/Ra. This range is similar to published values for silicate xenoliths of the East African Rift implying a local lithospheric mantle source for the volatile component of the Lengai magmas. It is still unclear if the natrocarbonatites themselves come from this region, or if fractionation and/or liquid immiscibility generate the carbonate magmas from a silicate melt within the crust itself.  相似文献   

15.
In the Jungwon area, South Korea, two contrasting types of deep thermal groundwater (around 20–33 °C) occur together in granite. Compared to shallow groundwater and surface water, thermal groundwaters have significantly lower δ18O and δD values (> 1‰ lower in δ18O) and negligible tritium content (mostly < 2 TU), suggesting a relatively high age of these waters (at least pre-thermonuclear period) and relatively long subsurface circulation. However, the hydrochemical evolution yielded two distinct water types. CO2-rich water (PCO2 = 0.1 to 2 atm) is characterized by lower pH (5.7–6.4) and higher TDS content (up to 3300 mg/L), whereas alkaline water (PCO2 = 10− 4.1–10− 4.6 atm) has higher pH (9.1–9.5) and lower TDS (< 254 mg/L). Carbon isotope data indicate that the CO2-rich water is influenced by a local supply of deep CO2 (potentially, magmatic), which enhanced dissolution of silicate minerals in surrounding rocks and resulted in elevated concentrations of Ca2+, Na+, Mg2+, K+, HCO3− and silica under lower pH conditions. In contrast, the evolution of the alkaline water was characterized by a lesser degree of water–rock (granite) interaction under the negligible inflow of CO2. The application of chemical thermometers indicates that the alkaline water represents partially equilibrated waters coming from a geothermal reservoir with a temperature of about 40 °C, while the immature characteristics of the CO2-rich water resulted from the input of CO2 in Na–HCO3 waters and subsequent rock leaching.  相似文献   

16.
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   

17.
Gas samples from some fumaroles at ‘La Fossa' crater and Baia di Levante on Vulcano Island and from a diffuse soil gas emission were analysed during 1995–1996, along with water samples from thermal wells in the area of Vulcano Porto. During 1996, we observed a significant increase both in the gas/steam ratio and in the CO2 concentration, as well as strong variations in δ13CCO2, δDH2O and δ18OH2O of fumarolic gases. These variations are probably related to an increased inflow of deep fluids of magmatic origin. The temperatures of fumaroles did not show remarkable variations except for fumarole F11. In this case, temperature increased by about 80°C from February to August 1996. During the same period, remarkable variations in temperature, phreatic level and chemical and isotopic composition of water were also recorded in one of the geothermal wells in the Vulcano Porto area (Camping Sicilia; T60°C). The observed variations in this well are probably related to a pressure build-up, occurring at least in the surficial part of the system, because of increased gas flux and/or decreased permeability of the fumarolic degassing system. Chemical and isotopic composition of the water showed that during this evolutionary phase, the content of fumarolic condensate in this well was about 80 to 90%. Based on the observation of physical and chemical variables of the Camping Sicilia fluids, during this phase of activity, it is concluded that this area is affected by a phreatic eruption hazard if a volcanic episode with high energy discharge in a limited time span occurs. It follows that this well may be considered as a preferential point for volcanic activity monitoring, both in the case of normal routine surveillance and in the case of inaccessibility to the crater area.  相似文献   

18.
Gas emissions from Erebus volcano, Antarctica, were measured by open-path Fourier transform infrared spectroscopy to understand degassing of its magmatic system. Two degassing phonolite lava lakes were present in the summit crater during observation in December 2004. We report analyses of H2O, CO2, CO, SO2, HF, HCl and OCS, (in order of molar abundance) in the plumes. Variations in the proportions of these species strongly reflect the dynamics of degassing, and sourcing of gas from different depths in the magmatic network. The highest observed ratios of CO2 and H2O are consistent with gas extracted from the melt at a depth of up to ∼ 2 km below the lava lakes. Magma degassing above this depth contributes to a higher H2O/CO2 proportion in the airborne plume. The ratio therefore reflects the balance of deeper vs. shallower contributions of volatiles and, possibly, a combination of closed- and open-system degassing. We observe a strong contrast in HF content in emissions from the two lava lakes, which we attribute to differing levels of magma ascent and/or cooling and crystallization of the magma supply. Fluxes of all gas species were determined using independent SO2 flux determinations and measured gas ratios. In the case of CO2 and water, ∼ 1 and ∼ 0.4 m3 s− 1, respectively, of parental basanite magma are required to sustain the calculated output. The discrepancy between the two figures is readily explained by sequestration of part of the magma supply at depth such that it only partially degasses its complement of water.  相似文献   

19.
This paper presents chemical and isotopic data for thermal waters, gases and S deposits from Volcan Puracé (summit elevation 4600 m) in SW Colombia. Hot gas discharges from fumaroles in and around the summit crater, and thermal waters discharge from three areas on its flanks. The waters from all areas have D values of-75±1, indicating a single recharge area at high elevation on the volcano. Aircorrected values of3He/4He in thermal waters range from 3.8 to 6.7 RA, and approach those for crater fumarole gas (6.1–7.1 RA), indicating widespread addition of magmatic volatiles. An economic S deposit (El Vinagre) is being mined in the Rio Vinagre fault zone at 3600 m elevation. Sulfur isotopic data are consistent with a magmatic origin for S species in thermal waters and gases, and for the S ore deposit. Isotopic equilibration between S species may have occurred at 220±40°C, which overlaps possible equilibration temperatures (170±40°C) determined by a variety of other geothermometers for neutral thermal waters. Apparent CH4–CO2 equilibration temperatures for gases from thermal springs (400±50°C) and crater fumaroles (520±60°C) reflect higher temperatures deeper in the system. Hot magmatic gas ascending through the Rio Vinagre fault zone is though to have precipitated S and generated thermal waters by interaction with descending meteoric waters.  相似文献   

20.
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   

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