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1.
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   

2.
Protozoan communities developed in laboratory microecosystems were used to evaluate the toxic effects of lead ion. The lead was added as lead acetate in different concentrations (50 g · l–1, 20 g · l–1, 10 g · l–1 and 1 g · l–1). The protozoans were taxonomically identified and classified into functional groups according to their common nutritional type. The population dynamics of protozoa has been studied. In the control the most frequent groups were bacterivore-detritivores and photosynthetics (more than 75% of abundance). Noticeable lead effects were observed after 24 hours of exposure to metal in all fractions. In general, the lead caused reductions in the number taxa, in total protozoan abundance and in protozoan biomass. The diversity values decreased in more than two nep respect to control in the different fractions. At the end of assay, the protozoan communities structure was simplified in the fractions with lead and some species of little flagellates were dominant. The information provided by this microecosystems of protozoan community was more complex than the one provided by single-species bioassays. Community protozoan bioassays may give more information about the toxic effects to compare with actual ecosystems.  相似文献   

3.
An experiment to ascertain the influence of artificially enhanced ammonium concentrations on riverine periphytic diatom communities was conducted during an 80 day period in winter 1988/89 (temperature: 5°C). During an initial 47 day enrichment phase, ammonium chloride at different concentrations was added to O2-saturated river water in experimental channels. Compared to a control, the addition of 1.2 mg NH 4 + -N·l–1 resulted in only slight changes in the species composition of the diatom community. The addition of 5.1 mg NH 4 + -N·l–1 and more (60 µg NH3-N·l–1) resulted in a decrease in the biomass and a drastic change in the species composition. After the 42 day enrichment period, the diatom speciesFragilaria capucina var.vaucheriae, Navicula saprophila, Navicula atomus andGomphonema parvulum, all of which are known to be tolerant to organic pollution, were found with relative abundances of 44.8%, 35.6%, 2.3% and 1.5%, respectively. Changes in species composition of the periphytic diatom communities occurred within the first two weeks of the subsequent recovery phase. After a month of recovery, all periphytic diatom communities exhibited a high degree of structural similarity with the control.  相似文献   

4.
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   

5.
Prealpine Lake Lungern shows in spite of low primary production rates (120 g C/m2. year) and full winter overturns a complete oxygen depletion in the deepest hypolimnion (65–70 m below surface) towards the end of summer stagnation. Periodical examinations of O2- and CH4-concentrations, CH4-oxidation rates and temperature in the water column during 1975/76 enabled an O2-balance of Lake Lungern. The direct measurement of the CH4-flux at the sediment-water-interface and of the CH4-concentrations in sediment cores as well as the determination of the age of methane bubbles lead to the conclusion, that the hypolimnic oxygen depletion is partly due to the oxidation of fossile methane penetrating the lake from below.   相似文献   

6.
Within one decade the yield in arctic char fishery of Lake Walenstadt (Switzerland) has dropped from 1.7 kg · ha–1 to 0.7 kg · ha–1. In the same period growth decreased by about 15%. The fish considered as degenerated dwarfed chars by fishermen are supposed to mature in very young ages.The change of the growth pattern can be related to reoligotrophication of the lake and impoverishments of the food source. Compared to other arctic char populations in Switzerland maturation takes place at least one year later.  相似文献   

7.
Lake Baringo, a freshwater lake in the central Kenya Rift Valley, is fed by perennial and ephemeral rivers, direct rainfall, and hot springs on Ol Kokwe Island near the centre of the lake. The lake has no surface outlet, but despite high evaporation rates it maintains dilute waters by subsurface seepage through permeable sediments and faulted lavas. New geochemical analyses (major ions, trace elements) of the river, lake, and hot spring waters and the suspended sediments have been made to determine the main controls of lake water quality. The results show that evaporative concentration and the binary mixing between two end members (rivers and thermal waters) can explain the hydrochemistry of the lake waters. Two zones are recognized from water composition. The southern part of the lake near sites of perennial river inflow is weakly influenced by evaporation, has low total dissolved species (TDS), and has a seasonally variable load of mainly detrital suspended sediments. In contrast, waters of the northern part of the lake show evidence for strong evaporation (TDS of up to eight times inflow). Authigenic clay minerals and calcite may be precipitating from those more concentrated fluids. The subaerial hot‐spring waters have a distinctive chemistry and are enriched in some elements that are also present in the lake water. Comparison of the chemical composition of the inflowing surface waters and lake water shows (1) an enrichment of some species (HCO3?, Cl, SO42?, F, Na, B, V, Cr, As, Mo, Ba and U) in the lake, (2) a depletion in SiO2 in the lake, and (3) a possible hydrothermal origin for most F. The rare earth element distribution and the F/Cl and Na/Cl ratios give valuable information on the rate of mixing of the river and hydrothermal fluids in the lake water. Calculations imply that thermal fluids may be seeping upward locally into the lake through grid‐faulted lavas, particularly south of Ol Kokwe Island. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

8.
The bottom sediment from three coring stations in Lake Lugano (Lago di Lugano) show major differences in their role in the P-cycles related to their geochemistry and characteristics of sedimentation. In the northern basin, the deepest sediment may be considered practically inactive, due to a permanently reduced condition at the sediment-water interface. In the southern basin, the sediments are active with respect to P-recycling with strong seasonal variations. One of the sites (Figino) behaves as a sink for P due to a high iron content and an important rate of detrital sedimentation.  相似文献   

9.
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10.
Data of hydrological and hydrochemical observations conducted in August 2000 at Lake Seliger and its major tributaries are presented. The analyzed characteristics included: O2, H2S, CH4, microelements; mineral and organic compounds of P and N, ionic composition components (HCO3 –, Cl–, Na+, K+, dry residue, pH; color index, electrical conductivity. Bottom sediment samples were analyzed for microelement concentrations, CH4, oil hydrocarbons. The influence of the basin on the ecological state of the lake was assessed, and tendencies in the evolution of its ecosystem are analyzed. It is shown that the ecological conditions of the lake has not changed significantly since 1960–1991, however, nutrient concentrations in the lake water was found to increase.  相似文献   

11.
Summary The surface thermal flux of the continental margins of the northwestern Mediterranean Sea is interpreted on the basis of a 1-D instantaneous pure shear stretching model of the lithosphere in terms of three components: the background heat flowing out from the asthenosphere (38 mW m–2), the transient contribution depending on the rift age and extension amount (35 mW m–2 at the most), and the contribution due to the radiogenic elements of the lithosphere. The radiogenic component is estimated at the continental margins of the Ligurian-Provençal basin and Valencia trough, and in the surrounding mainland areas by means of available data of surface heat generation from Variscan Corsica, Maures-Estérel and the Central Massif along with a geophysical-petrological relationship between heat production and seismic velocity. The lithosphere radiogenic heat contribution ql decreases with the thinning factor according to the exponential law: ql() = a exp(-b), in which factor b is greater for that part of the lithosphere below the uppermost 10 km. Considering also the heat generated by radioactive isotopes in sediments, the stable Variscan lithosphere produces an average thermal flux of 30 mW m–2 which decreases by about one half where the lithosphere is thinned by one third. Although the surface heat generation is 2·1 – 3·3 µW m–3 in the Maures-Estérel massif — excepting small outcrops of dioritic rocks with lower heat production — and 1·8 µW m–3 for most of Corsica, the radiogenic heating within the lithosphere for such areas is nearly the same and does not explain the higher heat flux of the Corsica margin. This asymmetric thermal pattern with surface heat flux which is 10 – 15 mW m–2 higher than predictions is probably of upper mantle origin, or can be ascribed to penetrative magmatism.  相似文献   

12.
Summary The normal type of serpentinites consists of chrysotile. The magnetite parts are essential parts of the structure of chrysotile serpentinites (primary magnetite). Chrysotile is changed to antigorite by mechanical deformations. The magnetite parts of rock structure are lost and they sat down in the veins of serpentinite rocks (secondary magnetite). In this paper the thermomagnetic diagrams and the results of X-ray investigations of secondary and primary magnetite are described. Some results of susceptibility measurements are given. The secondary magnetite is characterized by a region of oxydation in the interval 280–400° C (secondary magnetite-Fe2O3-Fe2O3). The oxydation to -Fe2O3 is remarkably. On the thermomagnetic diagrams of primary magnetite no typical oxydation region is to be seen. The oxydation: primary magnetite-Fe2O3 is very small. The interval of measured susceptibility values amounts to (10–1500)·10–6 cgs units. The essential variability of the main parts of serpentinite samples is characterized by the great changes of susceptibility values from point to point.The determined values of specific saturation magnetization (Gauss. cm3 g–1), the X-ray powder data, and some results on remanent magnetization are given.
Zusammenfassung Die Normaltypserpentinite bestehen aus Chrysotil. Der Magnetit ist Bestandteil der Struktur der Chrysotilserpentinite (primärer Magnetit). Unter dem Einfluß mechanischer Deformationen geht Chrysotil in Antigorit über. Die Magnetitanteile der Gesteinsstruktur gehen verloren und scheiden sich auf Klüften ab (sekundärer Magnetit). In der vorliegenden Arbeit werden die thermomagnetischen Abhängigkeiten und die Ergebnisse von Röntgenuntersuchungen des sekundären und primären Magnetits beschrieben. Es werden einige Ergebnisse der Suszeptibilitätsmessungen angeführt. Der sekundäre Magnetit wird durch einen Oxydationsbereich im Temperaturintervall 280–400° C charakterisiert (sekundärer Magnetit-Fe2O3-Fe2O3). Die Oxydation zu -Fe2O3 ist beträchtlich. Die thermomagnetischen Diagramme des primären Magnetits zeigen keinen typischen Oxydationsbereich. Die Oxydation: primärer Magnetit-Fe2O3 ist sehr gering. Das Intervall der gemessenen Suszeptibilitätswerte beträgt (10–1500)·10–6 CGS-Einheiten. Die starke Veränderlichkeit der Hauptbestandteile der Serpentinitproben wird durch die großen Änderungen der Suszeptibilitätswerte von Punkt zu Punkt gekennzeichnet.Die gemessenen Werte der Sättigungsmagnetisierung (Gauss.cm3 g–1), der Röntgenuntersuchungen und einige Ergebnisse über die remanente Magnetisierung werden gegeben.
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13.
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   

14.
A critical evaluation of literature values for the solubility products, K sp NBS = [Fe2+][HS–] Fe2+ HS– (H NBS + )–1, of various iron sulphide phases results in consensus values for the pKs of 2.95 ± 0.1 for amorphous ferrous sulphide, 3.6 ± 0.2 for mackinawite, 4.4 ± 0.1 for greigite, 5.1 ± 0.1 for pyrrhotite, 5.25 ± 0.2 for troilite and 16.4 ± 1.2 for pyrite.Where the analogous ion activity products have been measured in anoxic freshwaters in which there is evidence for the presence of solid phase FeS, the values lie within the range of 2.6–3.22, indicating that amorphous iron sulphide is the controlling phase. The single value for a groundwater of 2.65 (2.98 considering carbonate complexation) agrees. In seawater four values range between 3.85 to 4.2, indicating that mackinawite or greigite may be the controlling phase. The single low value of 2.94 is in a situation where particularly high fluxes of Fe (II) and S (–II) may result in the preferential precipitation of amorphous iron sulphide. Formation of framboidal pyrite in these sulphidic environments may occur in micro-niches and does not appear to influence bulk concentrations. Calculations show that the formation of Fe2S2 species probably accounts for very little of the iron or sulphide in most natural waters. Previously reported stability constants for the formation of Fe (HS)2 and (Fe (HS)3)– are shown to be suspect, and these species are also thought to be negligible in natural waters. In completely anoxic pore waters polysulphides also have a negligible effect on speciation, but in tidal sediments they may reach appreciable concentrations and lead to the direct formation of pyrite. Concentrations of iron and sulphide in pore waters can be controlled by the more soluble iron sulphide phase. The change in the IAP with depth within the sediment may reflect ageing of the solid phase or a greater flux of Fe (II) and S (–II) nearer the sediment surface. This possible kinetic influence on the value of IAPs has implications for their use in geochemical studies involving phase formation.  相似文献   

15.
A bathymetric survey of Kawah Ijen crater lake was conducted by acoustic sounding in 1996 to compare the lake morphology with those measured in 1922, 1925 and 1938, and to calculate the present lake volume. Even though the lake experienced several hydrothermal eruptions, the maximum depth became shallower (182 m) than before (200 m), resulting in a reduced lake volume (3.0×107 m3).Fifty-two major and minor constituents including rare earth elements and polythionates (PT) of the lake waters at various depths were determined by ICP-AES, ICP-MS and HPLC, respectively. These ions except for several volatile elements are taken up by lake fringe through congruent dissolution of pyroclastics of Kawah Ijen volcano. Most ions are homogeneously distributed throughout the lake, although PT showed a considerable vertical variation. Rare earth elements (REE) in the Kawah Ijen water as well as those from other hyper-acidic crater lakes show distribution patterns likely due to the three rock dissolution (preferential, congruent and residual) types, and their logarithmic concentrations linearly depend upon the pH values of the lake waters.Using the PT degradation kinetics data, production rates of PT, injection rates of SO2 and H2S into the lake were estimated to be 114, 86 and 30 tons/day, respectively. Also travel time of the spring water at the Banyupahit Riverhead from Kawah Ijen was estimated to be 600–1000 days through the consideration of decreasing rates of PT. Molten sulfur stocks containing Sn, Cu, Bi sulfides and Pb-barite exposed on the inner crater slope were presumed to be extinct molten sulfur pools at the former lake bottom. This was strongly supported by the barite precipitation temperature estimated through the consideration of the temperature dependence of Pb-chlorocomplex formation.  相似文献   

16.
Lake Albano, located 20 km to the SE of Rome, is hosted within the most recent crater of the quiescent Alban Hills volcanic complex that produced hydromagmatic eruptions in Holocene times. Stratigraphic, archaeological and historical evidence indicates that the lake level underwent important variations in the Bronze Age. Before the IV century B.C. several lahars were generated by water overflows from the lake and in the IV century B.C. Romans excavated a drainage tunnel. The lake is located above a buried carbonate horst that contains a pressurized medium-enthalpy geothermal reservoir from which fluids escape to the surface to produce many important gas manifestations of mostly CO2. Previous studies recognized the presence of gas emissions also from the crater bottom. In 1997 the possibility of a Nyos-type event triggered by a lake rollover was considered very low, because the CO2 water concentration at depth was found to be far from saturation. However, considering the high population density nearby, the Italian Civil Protection Department recommended that periodical monitoring be carried out. To this scope we initiated in 2001 a systematic geochemical study of the lake. Thirteen vertical profiles have been repeatedly carried out in 2001–2006, especially in the deepest part of the lake (167 m in 2006), measuring T, pH, dissolved O2 and electrical conductivity. Water samples were collected from various depths and chemically and isotopically analysed. Two similar profiles have been measured also in the nearby Nemi crater lake. Results indicate that in the 4.5 years of monitoring the pressure of gas dissolved in the Lake Albano deep waters remained much lower than the hydrostatic pressure. A CO2 soil survey carried out on the borders of the two lakes, indicates the presence of some zones of anomalous degassing of likely magmatic origin. A water overturn or a heavy mixing of deep and shallow waters likely occurred in winter 2003–2004, when cold rainfall cooled the surface water below 8.5 °C. Such overturns cause only a limited gas exsolution from the lake when the deep water is brought to a few meters depth but can explain the observed decrease with time of dissolved CO2 at depth and related water pH increase. A gas hazard could occur in the case of a sudden injection through the lake bottom of a huge quantity of CO2-rich fluids, which might be caused by earthquake induced fracturing of the rock pile beneath the lake. A limnic gas eruption might also occur should CO2 concentration build up within the lake for a long time.  相似文献   

17.
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   

18.
We estimate the response of chl-a (mg · m–3) to changes in concentrations of total phosphorus (TP) by calculating the slopeS = chl-a/TP in chl-a =f(TP) graphs. Results show that in years where algae are P-limited oligotrophic lakes respond less (median slope 0.21) to changes in nutrient concentrations than eutrophic lakes, (median slope 0.31) and these again less than hypereutrophic lakes, (median slope 1.02). We find no saturation value for the slope within the TP range considered (6–480 mg · m–3). Chl-a in eutrophic lakes responds more frequently to non-nutrient factors than oligotrophic and hypereutrophic lakes. Results obtained by replacing TP with a new nutrient parameter, TP = 0.056 · TP · IN0.226, in which inorganic nitrogen, IN, is factored in, suggest that nitrogen has an influence on chl-a in oligotrophic lakes. Blue-green algae respond less to changes in TP than other algal species, e.g., diatoms.  相似文献   

19.
The authors conducted a Rn222 survey in wells of the Larderello geothermal field (Italy) and observed considerable variations in concentrations. Simple models show that flow-rate plays an important part in the Rn222 content of each well, as it directly affects the fluid transit time in the reservoirs. Rn222 has been sampled from two wells of the Serrazzano area during flow-rate drawdown tests. The apparent volume of the steam reservoir of each of these two wells has been estimated from the Rn222 concentration versus flow-rate curves.List of symbols Q Flow-rate (kg h–1) - Decay constant of Rn222 (=7.553×10–3 h–1) - Porosity of the reservoir (volume of fluid/volume of rock) - 1 Density of the fluid in the reservoir (kg m–3) - 2 Density of the rock in the reservoir (kg m–3) - M Stationary mass of fluid filling the reservoir (kg). - E Emanating power of the rock in the reservoir (nCi kg rock –1 h–1). - P Production rate of Rn222 in the reservoir: number of atoms of Rn222 (divided by 1.764×107) transferred by the rock to the mass unit of fluid per unit time (nCi kg fluid –1 h–1). - N Specific concentration of Rn222 in the fluid (nCi kg–1) - Characteristic time of the steam reservoir at maximum flow-rate (=M/Q)  相似文献   

20.
Initial coagulation rates of colloidal hematite (-Fe2O3) particles (diameter less than 0.1 µm) were measured experimentally in well-defined laboratory systems at constant temperature. The relative stability ratio,W, was obtained at various ionic strengths in NaCl medium and at pH values in the range from 3 to 12. ExperimentalW values ranged from 1 to 104 in various systems. The results delineate the roles ofspecific andgeneralized coagulation mechanisms for iron oxides. Among the specifically-interacting species (G ads 0 >G coul 0 ) studied were phosphate, monomeric organic acids of various structures, and polymeric organic acids. The critical coagulation-restabilization concentrations of specifically-interacting anions (from 10–7 to 10–4 molar) can be compared with the general effects of non-specific electrolyte coagulants (10–3 to 10–1 molar). The laboratory results are interpreted with the help of a Surface Complex Formation/Diffuse Layer Model (SCF/DLM) which describes variations of interfacial charge and potential resulting from variations of coagulating species in solution. Comparison of these laboratory experiments with observations on iron behavior in estuarine and lake waters aids in understanding iron removal mechanisms and coagulation time scales in natural systems.  相似文献   

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