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1.
Monte-Carlo simulations were used to assess the extent of shortterm alkalinity depressions occuring in Sierra Nevada lakes due to acidic deposition events. The Episodic Event Model (EEM) was used to simulate spring snowmelt events. Snow course data, precipitation data and lake acidification surveys were used to derive values for the EEM parameters. Spring snowmelt events were shown to have great impacts on the water quality of Sierran lakes. Lakes are likely to be most affected by the early-spring snowmelt event because the epilimnion depth is at a minimum, which indicates minimum dilution. Under annual average loading conditions, no Sierran lake has been reported as acidic although 29% of the lakes have alkalinities less than 40 µeq/L indicating a sensitivity to acidification. In simulations of early-spring snowmelt events, using present-day acidic loading conditions, it was estimated 79% ± 9% of the lakes would experience shortterm lake alkalinity depressions to levels less than 40 µeq/L. The results provided by the model simulations are valuable in establishing upper and lower limits on the extent of possible episodic acidification to lake-resources-at-risk. The most critical parameters controlling the magnitude of lake alkalinity depressions during snowmelt episodic events are a) the lake area to watershed area ratio — a measure of input loading, and b) the epilimnion volume — a measure of dilution and mixing.  相似文献   

2.
Alpine lakes in siliceous catchments of Tyrol and Carinthia (Austria) show signs of acidification. About 9% of the studied lakes have no alkalinity, more than 20% are below pH 6. About two thirds of all lakes have acid neutralizing capacities below 100 eq 1–1. In spite of moderate precipitation acidity, some lakes show considerable concentrations of dissolved reactive aluminum during or shortly after snowmelt. High altitude lakes of the Alps are definitely more acidic than high mountain lakes in remote areas. Large differences in water and soil chemistry of nearby situated lakes were attributed to heterogeneities of bedrock geology. Paleolimnological investigations on former pH values of five lakes, based on diatom assemblages in the sediment, showed different developments: recent and past acidification, stable conditions, and alkalinization.  相似文献   

3.
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4.
The role of chemical weathering in the neutralization of acidic deposition   总被引：1，自引：0，他引：1  
Chemical weathering of rocks and minerals is a key factor which mitigates acidic deposition and affects water chemistry. It supplies cations and alkalinity to the surface water, groundwater, ion-exchange complex, and vegetation in the watershed. The kinetics of chemical weathering have not been determined in the field, but based on laboratory experiments, the rate of weathering has a fractional order dependency on hydrogen ion and organic ligand concentration in bulk solution. Watersheds with the greatest degree of hydrologic and geologic sensitivity can produce only 200–500 eq/ha·yr of cations or alkalinity for export. This is equivalent to 100 cm/yr of precipitation with a pH of 4.3–4.6 or an annual sulfur deposition of 1.0–2.5 g S/m2·yr. When acid and sulfur deposition are greater than these levels, extremely sensitive lakes may become acidified. To illustrate this point, a simple steady-state model is applied to lakes in regions where acidification of lakes has been reported.  相似文献   

5.
Although acidifying deposition in western North America is lower than in many parts of the world, many high‐elevation ecosystems there are extremely sensitive to acidification. Previous studies determined that the Mount Zirkel Wilderness Area (MZWA) has the most acidic snowpack and aquatic ecosystems that are among the most sensitive in the region. In this study, spatial and temporal variability of ponds and lakes in and near the MZWA were examined to determine their sensitivity to acidification and the effects of acidic deposition during and after snowmelt. Within the areas identified as sensitive to acidification based on bedrock types, there was substantial variability in acid‐neutralizing capacity (ANC), which was related to differences in hydrological flowpaths that control delivery of weathering products to surface waters. Geological and topographic maps were of limited use in predicting acid sensitivity because their spatial resolution was not fine enough to capture the variability of these attributes for lakes and ponds with small catchment areas. Many of the lakes are sensitive to acidification (summer and autumn ANC < 100 µeq L?1), but none of them appeared to be threatened immediately by episodic or chronic acidification. In contrast, 22 ponds had minimum ANC < 30 µeq L?1, indicating that they are extremely sensitive to acidic deposition and could be damaged by episodic acidification, although net acidity (ANC < 0) was not measured in any of the ponds during the study. The lowest measured pH value was 5·4, and pH generally remained less than 6·0 throughout early summer in the most sensitive ponds, indicating that biological effects of acidification are possible at levels of atmospheric deposition that occurred during the study. The aquatic chemistry of lakes was dominated by atmospheric deposition and biogeochemical processes in soils and shallow ground water, whereas the aquatic chemistry of ponds was also affected by organic acids and biogeochemical processes in the water column and at the sediment–water interface. These results indicate that conceptual and mechanistic acidification models that have been developed for lakes and streams may be inadequate for predicting acidification in less‐understood systems such as ponds. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

6.
Mean dissolved inorganic nitrogen concentrations ([DIN]) in deep, seasonally stratified lakes with comparable DIN inputs can differ by up to a factor of 3 depending on hydraulic and morphometric properties and/or different trophic states of the lakes. In such lakes, net N sedimentation rates were estimated with two independent methods (sediment core analysis and input-output mass balances). They were higher in eutrophic lakes (Mean: 5.1; SD: ± 1.6 g m–2 yr–1; n = 13) than in oligotrophic lakes (1.6 ± 1.0 g m–2 yr–1; n = 3), but independent of [DIN]. Gaseous N loss rates to the atmosphere, as calculated from combined N- and P-mass balances from selected lakes, ranged from 0.9 to 37.4 g m–2 yr–1 (n = 10) and were positively correlated with [DIN]. Reduction of NO 3 - to N2 is assumed to be the main cause for gaseous N losses. A simple one-box mass balance model for [DIN], based on DIN input and rates and kinetics of N removal processes (net sedimentation and gaseous N loss) is proposed, and validated with a data base on [DIN] and DIN input in 19 deep, seasonally stratified lakes of central Europe. The model illustrated that the amount of water loading per unit surface area of a lake (called water discharge height q) is the critical parameter determining mean lake [DIN] relative to mean input [DIN]. Lakes with a q > 50 m yr–1 have average [DIN] similar to the [DIN] of the inflows regardless of their trophic states, because input and outflow exceed lake-internal N removal processes. A high primary production favors DIN removal in lakes with q < 50 m yr–1. It is concluded that measures to decrease primary production, e.g. by means of P removal programs, lead to an increase of [DIN] in lakes.  相似文献   

7.
The southwestern Adirondack region of New York receives among the highest rates of atmospheric nitrogen (N) deposition in the USA. Atmospheric N deposition to sensitive ecosystems, like the Adirondacks, may increase the acidification of soils through losses of exchangeable nutrient cations, and the acidification of surface waters associated with enhanced mobility of nitrate (NO3?). However, watershed attributes, including surficial terrestrial characteristics, in‐lake processing, and geological settings, have been found to complicate the relationships between atmospheric N deposition and N drainage losses. We studied two lake‐watersheds in the southwestern Adirondacks, Grass Pond and Constable Pond, which are located in close proximity (～26 km) and receive similarly high N deposition, but have contrasting watershed attributes (e.g. wetland area, geological settings). Since the difference in the influence of N deposition was minimal, we were able to examine both within‐ and between‐watershed influences of land cover, the contribution of glacial till groundwater inputs, and in‐lake processes on surface water chemistry with particular emphasis on N solutes and dissolved organic carbon (DOC). Monthly samples at seven inlets and one outlet of each lake were collected from May to October in 1999 and 2000. The concentrations of NO3? were high at the Grass Pond inlets, especially at two inlets, and NO3? was the major N solute at the Grass Pond inlets. The concentrations of likely weathering products (i.e. dissolved Si, Ca2+, Mg2+, Na+) as well as acid neutralizing capacity and pH values, were also particularly high at those two Grass Pond inlets, suggesting a large contribution of groundwater inputs. Dissolved organic N (DON) was the major N solute at the Constable Pond inlets. The higher concentrations of DON and DOC at the Constable Pond inlets were attributed to a large wetland area in the watershed. The DOC/DON ratios were also higher at the Constable Pond inlets, possibly due to a larger proportion of coniferous forest area. Although DON and DOC were strongly related, the stronger relationship of the proportion of wetland area with DOC suggests that additional factors regulate DON. The aggregated representation of watershed physical features (i.e. elevation, watershed area, mean topographic index, hypsometric‐analysis index) was not clearly related to the lake N and DOC chemistry. Despite distinctive differences in inlet N chemistry, NO3? and DON concentrations at the outlets of the two lakes were similar. The lower DOC/DON ratios at the lake outlets and at the inlets having upstream ponds suggest the importance of N processing and organic N sources within the lakes. Although an inverse relationship between NO3? and DOC/DON has been suggested to be indicative of a N deposition gradient, the existence of this relationship for sites that receive similar atmospheric N deposition suggest that the relationship between NO3? and the DOC/DON ratio is derived from environmental and physical factors. Our results suggest that, despite similar wet N deposition at the two watershed sites, N solutes entering lakes were strongly affected by hydrology associated with groundwater contribution and the presence of wetlands, whereas N solutes leaving lakes were strongly influenced by in‐lake processing. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

8.
Monthly collections of phytoplankton were supported by physical–chemical data and measures of chlorophyll a concentrations in the search for particular environmental factors that could explain the constant presence of desmids in a Mexican tropical lake, a characteristic not common among the phytoplanktic communities of Mexican lakes. Samplings were taken from the water column in the deepest part of the lake (40 m) and intensified in the metalimnetic zone, whose establishment was monitored by observations of temperature and oxygen profiles. The general behavior of Lake Zirahuén was typical of warm monomictic tropical lakes at high elevation: a short mixing phase during the hemispheric winter. The depth of ZMIX and Zeu revealed a well-illuminated epilimnion, suggesting that phytoplankton communities are not likely to be light-limited. The oligotrophic nature of the lake is indicated by discrete concentrations of inorganic nutrients, PTOT in the interval of 0.01–0.03 mg l−1 and chlorophyll a between 0.23 and 3.98 μg l−1. These characteristics together with a low concentration of calcium, define a lacustrine environment different from other Mexican lakes, and one that could be suitable for desmids communities.  相似文献   

9.
Stable isotope compositions (δD, δ18O and δ34S) of volcanic lake waters, gas condensates and spring waters from Indonesia, Italy, Japan, and Russia were measured. The spring fluids and gas samples plot in a broad array between meteoric waters and local high-temperature volcanic gas compositions. The δD and δ18O data from volcanic lakes in East Indonesia plot in a concave band ranging from local meteoric waters to evaporated fluids to waters heavier than local high-temperature volcanic gases. We investigated isotopic fractionation processes in volcanic lakes at elevated temperatures with simultaneous mixing of meteoric waters and volcanic gases. An elevated lake water temperature gives enhanced kinetic isotope fractionation and changes in equilibrium fractionation factors, providing relatively flat isotope evolution curves in δ18O–δD diagrams. A numerical simulation model is used to derive the timescales of isotopic evolution of crater lakes as a function of atmospheric parameters, lake water temperature and fluxes of meteoric water, volcanic gas input, evaporation, and seepage losses. The same model is used to derive the flux magnitude of the Keli Mutu lakes in Indonesia. The calculated volcanic gas fluxes are of the same order as those derived from energy budget models or direct gas flux measurements in open craters (several 100 m3 volcanic water/day) and indicate a water residence time of 1–2 decades. The δ34S data from the Keli Mutu lakes show a much wider range than those from gases and springs, which is probably related to the precipitation of sulfur in these acid brine lakes. The isotopic mass balance and S/Cl values suggest that about half of the sulfur input in the hottest Keli Mutu lake is converted into native sulfur.  相似文献   

10.
Dissolved major ions, Sr concentrations and 87Sr/86Sr ratios of 10 coastal lakes from the Larsemann Hills, East Antarctica have been studied to constrain their solute sources, transport and glacial weathering patterns in their catchments. In absence of perennial river/streams, lakes serve as only reliable archive to study land surface processes in these low-temperature regions. The lake water chemistry is mostly Na-Cl type and it does not show any significant depth variations. Sr isotope compositions of these lakes vary from 0.7110 to 0.7211 with an average value of 0.7145, which is higher than modern seawater value. In addition to oceanic sources, major ions and Sr isotopic data show appreciable amount of solute supply from chemical weathering of silicate rocks in lake catchments and dissolution of Ca-Mg rich salts produced during the freezing of seawaters. The role of sulphide oxidation and carbonate weathering are found to be minimal on lake hydro-chemistry in this part of Antarctica. Inverse model calculations using this chemical dataset provide first-order estimates of dissolved cations and Sr; they are mostly derived from oceanic (seawater + snow) sources (cations approximately 76%) and (Sr approximately 92%) with minimal supplies from weathering of silicates (cations approximately 15%); (Sr approximately 2%) and Ca-rich minerals (cations approximately 9%); (Sr approximately 7%). The silicate weathering rate and its corresponding atmospheric CO2 consumption rate estimates for Scandrett lake catchment (3.6 ± 0.3 tons/km2/year and 0.5 × 105 moles/km2/year), are lower than that of reported values for the average global river basins (5.4 tons/km2/year and 0.9 × 105 tons/km2/year) respectively. The present study provides a comprehensive report of chemical weathering intensity and its role in atmospheric CO2 consumption in low-temperature pristine environment of Antarctica. These estimates underscore the importance of Antarctica weathering on atmospheric CO2 budget, particularly during the past warmer periods when the large area was exposed and available for intense chemical weathering.  相似文献   

11.
The abundance and the biomass of bacterial, phytoplanktonic, and ciliate communities were estimated at different depths during the spring planktonic development in an oligo-mesotrophic lake (the Pavin lake).The bacterial population, which consists mainly of free bacteria (94% of the total bacterial abundance), displays only low cell densities (0.6 to 7 × 105 cells · ml–1) and represents low biomass values (0.9 to 11.5 µgC·l–1) The bacteria represent from 0.9 to 23.8% (M = 9.7%) of the microplanktonic biomass (with the exclusion of heterotrophic nanoflagellates, i.e. bacteria + phytoplankton + ciliates, size range 0.2–160 µm). The abundance of the phytoplankton varies between 0.5 and 1.8 × 106 cells·l–1, and the biomass values between 12 and 118 µC·l–1. The phytoplankton population constitutes the largest part of the microplanktonic biomass (51.9 to 96.6%, M = 80.6%), and the diatomMelosira italica subsp.subarctica is the largely dominant species of this community. The population of ciliates, essentiallyOligotrichida andScuticociliatida, displays densities between 1.3 and 38.3 × 103 cells·l–1 (M = 6.7 × 103 cells·l–1), and biomass values vary from 0.10 to 16.30 µgC·l–1 (M = 6.01 µgC·l–1). The ciliates constitute thus from 0.1 to 26.4% (M = 9.8%) of the microplanktonic biomass. Whereas the oligotrichs are best represented in the euphotic zone, the small-sized scuticociliates dominate in the hypolimnion. Besides, species having symbionts and considered to be mixotrophic (Strobilidium gyrans, Strombidium viride, Stokesia vernalis) develop preferentially in the epilimnion and constitute more than 50% of the total ciliate biomass.  相似文献   

12.
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13.
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   

14.
Large lakes enclosures were used to examine the influence of nutrient (P, N) enrichment and planktivorous fish (1 + yellow perch) predation on hypolimnetic oxygen depletion. Results were compared to similar data for lakes with high (Lake St. George) and low (Haynes Lake) abundances of planktivorous fish. In both the unfertilized and fertilized enclosures, fish predation on large cladocerans increased the biomasses of pico- and nanoplankton (0.2–20 µm), phytoplankton (chlorophyll a) and total phosphorus (TP), reduced sedimentation, water clarity, and hypolimnetic oxygen concentrations (AHO). Fertilized enclosures without fish had highest TP and sedimentation rates, but the AHO were low. The high planktivore lake had higher pico- and nanoplankton, higher chlorophyll a, reduced water clarity, and lower AHO than the low planktivore lake. Areal hypolimnetic oxygen depletion (AHOD) rates were strongly related with Secchi depth and plankton size-distribution (r 2 = 0.77, and 0.79, respectively), but not as strongly with TP, chlorophyll a, and sedimentation rates (r 2 = 0.25, 0.53, and 0.02, respectively). Such observations are useful in forming a generalized hypothesis that lakes with low planktivory and high water clarity have lower oxygen depletion because 1) plankton that are settling are larger and spend less time in the hypolimnetic water column before reaching the sediment, and therefore undergo less decomposition, and 2) the euphotic depth extends into the hypolimnion and production of oxygen can take place.  相似文献   

15.
Environmental determinants of littoral paludification in boreal lakes   总被引：1，自引：0，他引：1  
Numerical studies of the relationships between littoral processes and environmental variables are important because they provide understanding of the impacts of natural and human factors on lake systems. In this study, littoral paludification, its occurrence, types and main environmental determinants were studied in boreal lakes with varying size (41–560 km2) and total phosphorus content (4.5–35.5 μg L−1) in Finland. The relative importance of catchment characteristics, water quality and water level regulation on paludification was analysed at the lake level (n=20), whereas the importance of site morphology, soil quality and aquatic vegetation was analysed at the site level (n=289). This study utilised two novel statistical methods in numerical analyses: generalised linear mixed models and variation partitioning (VP). Bottom ward overgrowth was the main paludification type in the studied lakes. At the lake level, the magnitude of spring flooding and the altitude of the lake had a negative response to paludification, whereas the existence of water level regulation, cover of clay soil and total phosphorus content correlated positively to paludification. At the site level, the paludification was negatively related to slope angle, and positively to the occurrence of clay soil, Glyceria maxima (reed sweet-grass) and the abundance of eutrophy indicator species. However, a considerable amount of variation in littoral paludification both at lake and site levels was accounted for by the joint effects of predictors and may thus be causally related to two or all three groups of predictors.  相似文献   

16.
A geochemical survey carried out in November 1993 revealed that Lake Quilotoa was composed by a thin (14 m) oxic epilimnion overlying a 200 m-thick anoxic hypolimnion. Dissolved CO2 concentrations reached 1000 mg/kg in the lower stratum. Loss of CO2 from epilimnetic waters, followed by calcite precipitation and a consequent lowering in density, was the apparent cause of the stratification.The Cl, SO4 and HCO3 contents of Lake Quilotoa are intermediate between those of acid–SO4–Cl Crater lakes and those of neutral-HCO3 Crater lakes, indicating that Lake Quilotoa has a ‘memory’ of the inflow and absorption of HC1- and S-bearing volcanic (magmatic) gases. The Mg/Ca ratios of the lake waters are governed by dissolution of local volcanic rocks or magmas, but K/Na ratios were likely modified by precipitation of alunite, a typical mineral in acid–SO4–Cl Crater lakes.The constant concentrations of several conservative chemical species from lake surface to lake bottom suggest that physical, chemical and biological processes did not have enough time, after the last overturn, to cause significant changes in the contents of these chemical species. This lapse of time might be relatively large, but it cannot be established on the basis of available data. Besides, the lake may not be close to steady state. Mixing of Lake Quilotoa waters could presently be triggered by either cooling epilimnetic waters by 4°C or providing heat to hypolimnetic waters or by seismic activity.Although Quilotoa lake contains a huge amount of dissolved CO2 (3×1011 g), at present the risk of a dangerous limnic eruption seems to be nil even though some gas exsolution might occur if deep lake waters were brought to the surface. Carbon dioxide could build up to higher levels in deep waters than at present without any volcanic re-awakening, due to either a large inflow of relatively cool CO2-rich gases, or possibly a long interval between overturns. Periodical geochemical surveys of Lake Quilotoa are, therefore, recommended.  相似文献   

17.
Two nanociliates of the order Prostomatida,Pseudobalanion planctonicum (12–18 µm) andUrotricha furcata (12–21 µm), were found to be the most abundant ciliates in the epilimnion of Piburger See, a small mesotrophic lake. Temperature and food availability were the main factors controlling the sudden increase in abundance, which reached a maximum of 101 cell ml–1 at the beginning of summer. During their exponential development in numbers and biomass, a strong decrease in chlorophylla and in the abundance of phytoplankton, especiallyRhodomonas, was observed. We assume, therefore, thatPseudobalanion planctonicum andUrotricha furcata together with rotifers, mainlyPolyarthra dolichoptera, are able to reduce the phytoplankton biomass in the upper epilimnion to the same level as found during the clearwater phase. Preliminary results of grazing on bacteria suggest that these nanociliates are omnivorous, although their impact on bacterial assemblages was low (3.1% of the standing stock grazed per day). Feeding on the base of the food web combined with their high abudance at certain times makes them an important link for higher trophic levels. This study constitutes the second report onPseudobalanion as an important component of the microbial food web in lakes.  相似文献   

18.
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   

19.
The effect of light intensity on the release of dissolved organic carbon during photosynthesis on NaH14CO3 was investigated using the phytoplanktonic CyanobacteriumOscillatoria rubescens. The released products were fractionated by molecular size and chemical identifications attempted using combined thin-layer electrophoresis and chromatography, and high pressure liquid chromatography.Within the range of irradiances tested (from 6 to 60 µmole m–2 sec–1), though the upper one inhibited photosynthesis ofO. rubescens, light had little effect on the quantity and composition of the excreted products. The released carbon was always lower than 3% of the incorporated carbon, and mainly composed (62 to 86%) by small molecular weight compounds. The prevailing identified compounds were amino acids which represented more than 20% of the excreted carbon. Among organic acids, glycolic acid accounted for less than 2% of the recovered radioactivity. Glucose was the only identified sugar.Abbreviations EOC excreted organic carbon - DOC dissolved organic carbon - PER percent extracellular release - LMW low molecular weight - HMW high molecular weight - AA amino acids - µmoles m–2 sec–1 = µEinsteins m–2 sec–1  相似文献   

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