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1.
Three crater lakes from Mexican volcanoes were sampled and analyzed at various dates to determine their chemical characteristics. Strong differences were observed in the chemistry among the three lakes: Nevado de Toluca, considered as dormant, El Chichón at a post-eruptive stage, and Popocatépetl at a pre-eruptive stage. Not surprisingly, no influence of volcanic activity was found at the Nevado de Toluca volcano, while the other volcanoes showed a correlation between the changing level of activity and the evolution of chemical trends. Low pHs (<3.0) were measured in the water from the active volcanoes, while a pH of 5.6 was measured at the Nevado de Toluca Sun lake. Changes with time were observed at Popocatépetl and El Chichón. Concentrations of volcanic-gas derived species like Cl−, SO42− and F− decreased irregularly at El Chichón from 1983 until 1997. Major cations concentrations also diminished at El Chichón. A 100% increase in the SO42− content was measured at Popocatépetl between 1985 and 1994. An increase in the Mg/Cl ratio between 1992 (Mg/Cl=0.085) and 1994 (Mg/Cl=0.177) was observed at Popocatépetl, before the disappearance of the crater lake in 1994. It is concluded that chemical analysis of crater lakes may provide a useful additional tool for active-volcano monitoring.  相似文献   

2.
Leachates from ash samples of the Popocatépetl eruptions of April 30, 1996, May 12, 1997, and October 17, 1998 settled at different distances from the crater were analyzed for anions (SO42−, Cl−, F−) and some metals. This study is aimed at determining the causes of the compositional variations of the leachates, to assist the assessment of water, soil and crop contamination due to ash deposits. Different behavior was observed in the ion concentrations with distance for the three eruptions. On April 30, 1996, SO42− and F− concentrations increased with distance, and Cl− remained almost constant. On May 12, 1997, concentrations of the three anions decreased with distance. On October 17, 1998, F−, Cl− and SO42− increased more than three-fold with distance. Tephra size distributions were also different for the three eruptions. The observed trends of the leachates’ anion concentrations may have different causes: the type and intensity of the eruptions, the distribution of the tephra sizes, the degree of interaction of the tephras with volcanic gases, humidity, static charge, the original characteristics of the solid material, the transport time from the crater to the site of settling, and the relative angle between the wind direction and the sampling line. Enrichment factors and concentration trends for metals with distance suggest that Co, Ni, Cu and Pb in the leachates resulted mostly from volcanic gas adsorption.  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.
Sulfur isotope effects during the SO2 disproportionation reaction to form elemental sulfur (3SO2+3H2O→2HSO4−+S+2H+) at 200–330°C and saturated water vapor pressures were experimentally determined. Initially, a large kinetic isotopic fractionation takes place between HSO4− and S, followed by a slow approach to equilibrium. The equilibrium fractionation factors, estimated from the longest run results, are expressed by 1000 ln αHSO4−–S=6.21×106/T2+3.62. The rates at which the initial kinetic fractionation factors approach the equilibrium ones were evaluated at the experimental conditions.δ34S values of HSO4− and elemental sulfur were examined for active crater lakes including Noboribetsu and Niseko, (Hokkaido, Japan), Khloridnoe, Bannoe and Maly Semiachik (Kamchatka), Poás (Costa Rica), Ruapehu (New Zealand) and Kawah Ijen and Keli Mutu (Indonesia). ΔHSO4−–S values are 28‰ for Keli Mutu, 26‰ for Kawah Ijen, 24‰ for Ruapehu, 23‰ for Poás, 22‰ for Maly Semiachik, 21‰ for Yugama, 13‰ for Bannoe, 9‰ for Niseko, 4‰ for Khloridonoe, and 0‰ for Noboribetsu, in the decreasing order. The SO2 disproportionation reaction in the magmatic hydrothermal system below crater lakes where magmatic gases condense is responsible for high ΔHSO4−–S values, whereas contribution of HSO4− produced through bacterial oxidation of reduced sulfur becomes progressively dominant for lakes with lower ΔHSO4−–S values. Currently, Noboribetsu crater lake contains no HSO4− of magmatic origin. A 40-year period observation of δ34SHSO4− and δ34SS values at Yugama indicated that the isotopic variations reflect changes in the supply rate of SO2 to the magmatic hydrothermal system. This implies a possibility of volcano monitoring by continuous observation of δ34SHSO4− values. The δ18O values of HSO4− and lake water from the studied lakes covary, indicating oxygen isotopic equilibration between them. The covariance gives strong evidence that lake water circulates through the sublimnic zone at temperatures of 140±30°C.  相似文献   

5.
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   

6.
Emission rates of sulfur dioxide (SO2) were measured at Erebus volcano, Antarctica in December between 1992 and 2005. Since 1992 SO2 emissions rates are normally distributed with a mean of 61 ± 27 Mg d− 1 (0.7 ± 0.3 kg s− 1) (n = 8064). The emission rates vary over minutes, hours, days and years. Hourly and daily variations often show systematic and cyclic trends. Long-wavelength, large amplitude trends appear related to lava lake area and both are likely controlled by processes occurring at depth. Time series analysis of continuous sequences of measurements obtained over periods of several hours reveals periodicity in SO2 output ranging from 10 to 360 min, with a 10 min cycle being the most dominant. Closed and open-system degassing models are considered to explain observed variable degassing rates. Closed-system degassing is possible as rheological stiffening and stick/slip may occur within the system. However, the timescales represented in these models do not fit observations made on Erebus. Open-system degassing and convection fits the observations collected as the presented models were developed for a system similar to Erebus in terms of degassing, eruptive activity and process repose time. We show that with the observed emission rate (0.71 kg s− 1) and a crystal content of 30%, magma will cool 65 °C to match observed heat fluxes; this cooling is sufficient enough to drive convection.  相似文献   

7.
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   

8.
Since the March–April 1982 eruption of El Chichòn volcano, intense hydrothermal activity has characterised the 1-km-wide summit crater. This mainly consists of mud and boiling pools, fumaroles, which are mainly located in the northwestern bank of the crater lake. During the period 1998–2000, hot springs and fumaroles discharging inside the crater and from the southeastern outer flank (Agua Caliente) were collected for chemical analyses. The observed chemical fluctuations suggest that the physico-chemical boundary conditions regulating the thermodynamic equilibria of the deep rock/fluid interactions have changed with time. The chemical composition of the lake water, characterised in the period 1983–1997 by high Na+, Cl−, Ca2+ and SO42− contents, experienced a dramatic change in 1998–1999, turning from a Na+–Cl−- to a Ca2+–SO42−-rich composition. In June 2000, a relatively sharp increase in Na+ and Cl− contents was observed. At the same time, SO2/H2S ratios and H2 and CO contents in most gas discharges increased with respect to the previous two years of observations, suggesting either a new input of deep-seated fluids or local variations of the more surficial hydrothermal system. Migration of gas manifestations, enhanced number of emission spots and variations in both gas discharge flux and outlet temperatures of the main fluid manifestations were also recorded. The magmatic-hydrothermal system of El Chichòn is probably related to interaction processes between a deep magmatic source and a surficial cold aquifer; an important role may also be played by the interaction of the deep fluids with the volcanic rocks and the sedimentary (limestone and evaporites) basement. The chemical and physical changes recorded in 1998–2000 were possibly due to variations in the permeability of the conduit system feeding the fluid discharges at surface, as testified by the migration of gas and water emanations. Two different scenarios can be put forward for the volcanic evolution of El Chichòn: (1) build-up of an infra-crater dome that may imply a future eruption in terms of tens to hundreds of years; (2) minor phreatic–phreatomagmatic events whose prediction and timing is more difficult to constrain. This suggests that, unlike the diminished volcanic activity at El Chichòn after the 1982 paroxistic event, the volcano-hydrothermal fluid discharges need to be more constantly monitored with regular and more frequent geochemical sampling and, at the same time, a permanent network of seismic stations should be installed.  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.
A miniaturized, lightweight and low-cost UV correlation spectrometer, the FLYSPEC, has been developed as an alternative for the COSPEC, which has long been the mainstay for monitoring volcanic sulfur dioxide fluxes. Field experiments have been conducted with the FLYSPEC at diverse volcanic systems, including Masaya (Nicaragua), Poás (Costa Rica), Stromboli, Etna and Vulcano (Italy), Villarica (Chile) and Kilauea (USA). We present here those validation measurements that were made simultaneously with COSPEC at Kilauea between March 2002 and February 2003. These experiments, with source emission rates that ranged from 95 to 1,560 t d−1, showed statistically identical results from both instruments. SO2 path-concentrations ranged from 0 to >1,000 ppm-m with average correlation coefficients greater than r 2=0.946. The small size and low cost create the opportunity for FLYSPEC to be used in novel deployment modes that have the potential to revolutionize the manner in which volcanic and industrial monitoring is performed.  相似文献   

11.
Stable isotope ratios of S, O and Sr have been measured for active vent materials which were first found and sampled in April 1987 from the Mariana backarc spreading axis at 18°N. Chimneys consisted mostly of barite with a lesser proportion of sulfide minerals such as sphalerite, galena, chalcopyrite and pyrite. Theδ34S values of sphalerite and galena taken from several chimneys and various parts of a chimney showed a narrow range from 2.1 to 3.1‰, suggesting uniform conditions of fluid chemistry during chimney growth. The sulfur isotopic results imply a contribution of hydrogen sulfide reduced from seawater sulfate in the deep hydrothermal reaction zone, considering that fresh glasses of the Mariana Trough basalts haveδ34S= −0.6 ± 0.3‰. Sulfur isotopic compositions of hydrogen sulfide in the high temperature vent fluids (δ34S= 3.6–4.8‰) which are higher than those of the sulfide minerals suggest the secondary addition of hydrogen sulfide partially reduced from entrained seawater SO42− at a basal part of the chimneys. This interpretation is consistent with theδ34S values of barite (21–22‰) that are higher than those of seawater sulfate. The residence time of the entrained SO42− was an order of an hour on a basis of oxygen isotopic disequilibrium of barite. Strontium isotopic variations of barite and vent waters indicated that Sr in barite was mostly derived from the Mariana Trough basalts with a slight contribution from Sr in circulating sea-water, and that 10–20% mixing of seawater with ascending hydrothermal fluids induced precipitation of barite at the sea-floor.  相似文献   

12.
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   

13.
The Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) is a useful tool for detecting low quantities of sulfur dioxide at passively degassing volcanoes such as Lascar volcano, Chile. Two mini-UV spectrometers (MUSes) were used to make transects of Lascar volcano’s sulfur dioxide plume on December 7, 2004, during a coordinated overpass of ASTER. SO2 burdens were retrieved using the thermal infrared channels of the acquired ASTER image. This allowed for a direct comparison between the two methods in order to validate the ASTER SO2 retrieval. The results were extremely encouraging with ASTER deriving SO2 fluxes within the range of fluxes obtained by the MUSe.  相似文献   

14.
Kawah Putih is a summit crater of Patuha volcano, West Java, Indonesia, which contains a shallow, 300 m-wide lake with strongly mineralized acid–sulfate–chloride water. The lake water has a temperature of 26–34°C, pH=<0.5–1.3, Stot=2500–4600 ppm and Cl=5300–12 600 ppm, and floating sulfur globules with sulfide inclusions are common. Sulfur oxyanion concentrations are unusually high, with S4O62−+S5O62−+S6O62−=2400 – 4200 ppm. Subaerial fumaroles (<93°C) on the lake shore have low molar SO2/H2S ratios (<2), which is a favorable condition to produce the observed distribution of sulfur oxyanion species. Sulfur isotope data of dissolved sulfate and native sulfur show a significant 34S fractionation (ΔSO4–Se of 20‰), probably the result of SO2 disproportionation in or below the lake. The lake waters show strong enrichments in 18O and D relative to local meteoric waters, a result of the combined effects of mixing between isotopically heavy fluids of deep origin and meteoric water, and evaporation-induced fractionation at the lake surface. The stable-isotope systematics combined with energy-balance considerations support very rapid fluid cycling through the lake system. Lake levels and element concentrations show strong seasonal fluctuations, indicative of a short water residence time in the lake as well.Thermodynamic modeling of the lake fluids indicates that the lake water is saturated with silica phases, barite, pyrite and various Pb, Sb, Cu, As, Bi-bearing sulfides when sulfur saturation is assumed. Precipitating phases predicted by the model calculations are consistent with the bulk chemistry of the sulfur-rich bottom sediments and their identified mineral phases. Much of the lake water chemistry can be explained by congruent rock dissolution in combination with preferential enrichments from entering fumarolic gases or brines and element removal by precipitating mineral phases, as indicated by a comparison of the fluids, volcanic rocks and lake bed sediment.Flank springs on the mountain at different elevations vary in composition, and are consistent with local rock dissolution as a dominant factor and pH-dependent element mobility. Discharges of warm sulfate- and chloride-rich water at the highest elevation and a near-neutral spring at lower level may contain a small contribution of crater-lake water. The acid fluid-induced processes at Patuha have led to the accumulation of elements that are commonly associated with volcano-hosted epithermal ore deposits. The dispersal of heavy metals and other potentially toxic elements from the volcano via the local drainage system is a matter of serious environmental concern.  相似文献   

15.
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   

16.
Samples from Kawah Ijen crater lake, spring and fumarole discharges were collected between 1990 and 1996 for chemical and isotopic analysis. An extremely low pH (<0.3) lake contains SO4–Cl waters produced during absorption of magmatic volatiles into shallow ground water. The acidic waters dissolve the rock isochemically to produce “immature” solutions. The strong D and 18O enrichment of the lake is mainly due to enhanced evaporation at elevated temperature, but involvement of a magmatic component with heavy isotopic ratios also modifies the lake D and 18O content. The large ΔSO4–S0 (23.8–26.4‰) measured in the lake suggest that dissolved SO4 forms during disproportionation of magmatic SO2 in the hydrothermal conduit at temperatures of 250280°C. The lake δ18OSO4 and δ18OH2O values may reflect equilibration during subsurface circulation of the water at temperatures near 150°C. Significant variations in the lake's bulk composition from 1990 to 1996 were not detected. However, we interpret a change in the distribution and concentration of polythionate species in 1996 as a result of increased SO2-rich gas input to the lake system.Thermal springs at Kawah Ijen consist of acidic SO4–Cl waters on the lakeshore and neutral pH HCO3–SO4–Cl–Na waters in Blawan village, 17 km from the crater. The cation contents of these discharges are diluted compared to the crater lake but still do not represent equilibrium with the rock. The SO4/Cl ratios and water and sulfur isotopic compositions support the idea that these springs are mixtures of summit acidic SO4–Cl water and ground water.The lakeshore fumarole discharges (T=170245°C) have both a magmatic and a hydrothermal component and are supersaturated with respect to elemental sulfur. The apparent equilibrium temperature of the gas is 260°C. The proportions of the oxidized, SO2-dominated magmatic vapor and of the reduced, H2S-dominated hydrothermal vapor in the fumaroles varied between 1979 and 1996. This may be the result of interaction of SO2-bearing magmatic vapors with the summit acidic hydrothermal reservoir. This idea is supported by the lower H2S/SO2 ratio deduced for the gas producing the SO4–Cl reservoir feeding the lake compared with that observed in the subaerial gas discharges. The condensing gas may have equilibrated in a liquid–vapor zone at about 350°C.Elemental sulfur occurs in the crater lake environment as banded sediments exposed on the lakeshore and as a subaqueous molten body on the crater floor. The sediments were precipitated in the past during inorganic oxidation of H2S in the lake water. This process was not continuous, but was interrupted by periods of massive silica (poorly crystallized) precipitation, similar to the present-day lake conditions. We suggest that the factor controlling the type of deposition is related to whether H2S- or silica-rich volcanic discharges enter the lake. This could depend on the efficiency with which the lake water circulates in the hydrothermal cell beneath the crater. Quenched liquid sulfur products show δ34S values similar to those found in the banded deposits, suggesting that the subaqueous molten body simply consists of melted sediments previously accumulated at the lake bottom.  相似文献   

17.
Uzon caldera, located in the eastern volcanic belt of the Kamchatka peninsula, is a complicated structure of Middle Pleistocene age. The composition of the co-existing solid and fluid phases, temperature and pH were determined with the aim of establishing the distribution of sulphur species, As, Sb and the main ore-forming metals. In the solid samples, the following sulphur-bearing minerals were identified: pyrite, realgar, orpiment, alacranite (As8S9), uzonite (As4S5), amorphous As-sulphide, stibnite, cinnabar and native sulphur. The following sulphur-bearing species H2S, H2S2+S52−(aq)(aqueous polysulphanes), S0(aq), SO32−(aq), S2O32−, SO42− and total concentration of sulphur were determined in solutions. Eh, pH and H2S concentration were measured potentiometrically in situ. Zero-valent sulphur (S0(aq)+H2S2+S52−(aq)) predominates in Uzon solutions. The pair H2S–Scolloidal is Eh-determining in Uzon solutions up to 75–85°C. A quantitative thermodynamic model of the mineral deposition process at Uzon was constructed using the collected data. It was obtained that the composition of the hydrothermal solution and the precipitation of Sb–As–Hg species can be described using two only main factors: the initial composition of fluid and the temperature variation.  相似文献   

18.
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   

19.
In the present work, we built a mathematical model of polychlorinated biphenyl (PCB) bioaccumulation in Perna viridis, namely, a one-compartment model with a time dependent incorporation rate R (μg g−1 lipid per ppb water per day), with positive substrate cooperativity as the underlying physical mechanism. The temporal change of the PCB concentration Q (μg g−1 lipid) in the soft tissues of the mussel depends on the competition of the input rate RW and the output rate kQ, where W is the concentration of PCB in water (ppb water) and k is the elimination rate (per day). From our experimental data, k=0.181±0.017 d−1. The critical concentration in water Wc for positive substrate cooperativity was found to be 2.4 ppb. Below Wc, R is a constant. For a water concentration of 0.5 ppb Aroclor 1254, R=24.0±2.4 μg g−1 lipid ppb−1 d−1. Above Wc, positive substrate cooperativity comes into effect and R becomes a function of time and dependent on the concentration Q in a form R=γQ/(Q+δ). This is the case for a water concentration of 5 ppb Aroclor 1254, where γ=15.1 μg g−1 lipid ppb−1 d1 and δ≈200 μg g−1 lipid. From this model, the uptake is exponentially increasing when the PCB concentration in the mussel is small compared to 200 μg g−1 lipid, and hyperbolically increasing when the concentration is large compared to 200 μg g−1 lipid, which are consistent with the experimental data. The model is useful for understanding the true processes taking place during the bioaccumulation and for risk assessment with higher confidence. Future experimental data which challenge the present model are anticipated and in fact desirable for improvement and perfection of the model.  相似文献   

20.
Radionuclide activities (210Pb, 210Bi, 210Po) were investigated in Mount Etna plume from 1983 to 1995. At SE crater the long-term observation (12 years) of the 210Po/210Pb ratio shows that it can behave as a degassing vent not directly related to the main magma reservoir depending on the magma level inside the volcano. Since 1992, the simultaneous determination of radionuclides and sulfur in the main plume results in new constraints on the degassing model of Lambert et al. (Earth Planet. Sci. Lett., 76 (1986) 185). The 210Po/SO2 and 210Pb/SO2 ratios enable us to identify two sources of 210Po in the plume: one is magmatic, correlated with SO2, the other one is an additional component issued from the decay of 210Pb in the shallow degassing cell, and depends directly on the residence time of the gases before their emission. Estimations of the volume of degassing magma, the residence time of the gases and the proportion of undegassed magma renewing the shallow degassing cell are given for the period 1992–1995. During the 1992 eruption, the rate of degassing magma volume is estimated to have been as high as 5×106 m3/day, and the volume of the shallow degassing magma reservoir about 0.5 km3. In 1994 and 1995 the rate of non-erupted degassing magma volume was estimated to have been about 0.18 km3/year. During the entire 1983–1995 period, only 15–20% of the degassed magma was erupted.  相似文献   

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