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1.
[Cu2+] and Cu complexation parameters in some selected freshwater systems in Switzerland were determined by the technique of ligand-exchange and DPCSV. Results from the water columns of some eutrophic and oligotrophic lakes are presented and compared to small acid lakes. Cu is strongly complexed by organic ligands which with very high stability constants at low concentrations are probably biologically produced, as indicated by the seasonal variations in the eutrophic lakes and by the relationship between Cu complexation and algal activity in the eutrophic (pCu=15–16), oligotrophic (pCu=13–14) and acidic (pCu=9–10) lakes. The extent of Cu complexation in river waters was generally lower than in the eutrophic lakes, at similar DOC levels. No obvious correlation between Cu complexation and DOC was observed, indicating that Cu complexing ligands are specific organic compounds.  相似文献   

2.
The seasonal variability of the distribution of dissolved forms of mineral phosphorus and silicon and water alkalinity is studied in the Northern Dvina River mouth. The non-conservative behavior of mineral phosphorus and silicon (presumably caused by the biological consumption of these elements) and the conservative distribution of alkalinity are established. The conservative distribution of alkalinity makes it possible to use the relationship between the values of this parameter and the concentrations of chlorides for the analysis of the genetic structure of water in the desalinized part of the Baltic Sea.__________Translated from Vodnye Resursy, Vol. 32, No. 4, 2005, pp. 459–463.Original Russian Text Copyright © 2005 by Savenko, Shevchenko.  相似文献   

3.
The Latera field (Vulsini volcanic complex, Latium, Italy) is one of the geothermal areas of the peri-Tyrrhenian belt along which a regional, high thermal anomaly has been detected. So far nine deep wells have been drilled within the Latera caldera and four of them have been productive. The geothermal reservoir is located within the fractured carbonatic rocks of the Tuscan nappe; the overlying volcanic units, sealed by hydrothermal minerals (mainly calcite and anhydrite), act as an impervious cover.The fluid produced by the wells comes from a deep aquifer (about 1000–1500 m depth) which at present is not connected with the shallow aquifer in the volcanoclastic units. Fluid temperatures range between 200 and 230°C; in-hole temperatures as high as 343°C at 2775 m depth have been measured in dry wells.The study of the newly formed mineral assemblages from both volcanic and sedimentary units as sampled from the geothermal wells can be used to reconstruct the thermal evolution of the geothermal field. The intrusion of a syenitic melt, up to a depth of about 2000 m, dated 0.86 Ma, represents the major thermal event for the units in the area and is assumed to represent the first step in the geothermal evolution of the Latera system.The above mentioned newly formed mineral assemblages can be divided into three groups: (a) “contact-metasomatic”: calcite, anhydrite, diopsidic pyroxene, grossularitic garnet, phlogopite, wollastonite or monticellite; (b) “high-temperature hydrothermal”: calcite, anhydrite, K-feldspar, vesuvianite, melanitic garnet, tourmaline, amphibole, epidote, sulphides; (c) “low-temperature hydrothermal”: calcite, anhydrite, K-feldspar, clay minerals, sulphides. Group (a) minerals are now relics. Part of (b) and all of (c) group are still in equilibrium with the existing conditions in different parts of the geothermal system.Thermodynamic calculations on the observed mineral assemblages permitted estimates of the P, T conditions and gas fugacities.  相似文献   

4.
The carbon isotopic composition of diagenetic dolomite and calcite in some sediments of the Gulf of Mexico varies between “normal-marine” (δ13C ca. 0‰) and −14.6‰ which suggests that biogenic CO2 contributed to the carbonate formation. The δ13O values of dolomite and coexisting calcite are very similar but variable down-core.Dolomite and calcite precipitated early from pore water where SO42− was not reduced. However, during (and after?) SO42− reduction dolomite and calcite still formed and there are at least two generations of carbonate minerals present.  相似文献   

5.
Cave air PCO2 at two Irish sites varied dramatically on daily to seasonal timescales, potentially affecting the timing of calcite deposition and consequently climate proxy records derived from stalagmites collected at the same sites. Temperature-dependent biochemical processes in the soil control CO2 production, resulting in high summer PCO2 values and low winter values at both sites. Large Large-amplitude, high-frequency variations superimposed on this seasonal cycle reflect cave air circulation. Here we model stalagmite growth rates, which are controlled partly by CO2 degassing rates from drip water, by considering both the seasonal and high-frequency cave air PCO2 variations. Modeled hourly growth rates for stalagmite CC-Bil from Crag Cave in SW Ireland reach maxima in late December (0.063 μm h− 1) and minima in late June/early July (0.033 μm h− 1). For well-mixed ‘diffuse flow’ cave drips such as those that feed CC-Bil, high summer cave air PCO2 depresses summer calcite deposition, while low winter PCO2 promotes degassing and enhances deposition rates. In stalagmites fed by well-mixed drips lacking seasonal variations in δ18O, integrated annual stalagmite calcite δ18O is unaffected; however, seasonality in cave air PCO2 may influence non-conservative geochemical climate proxies (e.g., δ13C, Sr/Ca). Stalagmites fed by ‘seasonal’ drips whose hydrochemical properties vary in response to seasonality may have higher growth rates in summer because soil air PCO2 may increase relative to cave air PCO2 due to higher soil temperatures. This in turn may bias stalagmite calcite δ18O records towards isotopically heavier summer drip water δ18O values, resulting in elevated calcite δ18O values compared to the ‘equilibrium’ values predicted by calcite–water isotope fractionation equations. Interpretations of stalagmite-based paleoclimate proxies should therefore consider the consequences of cave air PCO2 variability and the resulting intra-annual variability in calcite deposition rates.  相似文献   

6.
To improve understanding of Ca isotope transport during water-rock interaction on the continents, we measured dissolved δ44Ca values along a 236 km flow path in the Madison aquifer, South Dakota, where fluids have chemically evolved according to dolomite and anhydrite dissolution, calcite precipitation, and Ca-for-Na ion-exchange over a timescale spanning ~ 15 kyr. We used a reactive transport model employing rate data constrained from major ion mass-balances to evaluate the extent to which calcite precipitation and ion-exchange fractionate Ca isotopes. Elevated δ44Ca values during the initial and final stages of water transport possibly result from calcite precipitation under supersaturated conditions and Ca-for-Na ion-exchange, respectively. However, for the bulk of the flow path, δ44Ca values evolve by mixing between anhydrite and dolomite dissolution, with no fractionation during calcite precipitation under saturated conditions. We attribute the absence of Ca isotope fractionation to the long timescale of water-rock interaction and slow rate of calcite precipitation, which have enabled fluids to chemically and isotopically equilibrate with calcite. We therefore conclude that the equilibrium Ca isotope fractionation factor between calcite and water (Δcal–w) is very close to zero. To the extent that the Madison aquifer typifies other groundwater systems where calcite slowly precipitates from solutions at or near chemical equilibrium, this study suggests that groundwater contributions to δ44Ca variability on the continents can be modeled according to simple mixing theory without invoking isotope discrimination.  相似文献   

7.
This study is undertaken to understand how calcite precipitation and dissolution contributes to depth-related changes in porosity and permeability of gas-bearing sandstone reservoirs in the Kela 2 gas field of the Tarim Basin, Northwestern China. Sandstone samples and pore water samples are col-lected from well KL201 in the Tarim Basin. Vertical profiles of porosity, permeability, pore water chem-istry, and the relative volume abundance of calcite/dolomite are constructed from 3600 to 4000 m below the ground surface within major oil and gas reservoir rocks. Porosity and permeability values are in-versely correlated with the calcite abundance, indicating that calcite dissolution and precipitation may be controlling porosity and permeability of the reservoir rocks. Pore water chemistry exhibits a sys-tematic variation from the Na2SO4 type at the shallow depth (3600-3630 m), to the NaHCO3 type at the intermediate depth (3630―3695 m),and to the CaCl2 type at the greater depth (3728―3938 m). The geochemical factors that control the calcite solubility include pH, temperature, pressure, Ca2 concen-tration, the total inorganic carbon concentration (ΣCO2), and the type of pore water. Thermodynamic phase equilibrium and mass conservation laws are applied to calculate the calcite saturation state as a function of a few key parameters. The model calculation illustrates that the calcite solubility is strongly dependent on the chemical composition of pore water, mainly the concentration difference between the total dissolved inorganic carbon and dissolved calcium concentration (i.e., [ΣCO2] -[Ca2 ]). In the Na2SO4 water at the shallow depth, this index is close to 0, pore water is near the calcite solubility. Calcite does not dissolve or precipitate in significant quantities. In the NaHCO3 water at the intermedi-ate depth, this index is greater than 0, and pore water is supersaturated with respect to calcite. Massive calcite precipitation was observed at this depth interval and this intensive cementation is responsible for decreased porosity and permeability. In the CaCl2 water at the greater depth, pore water is un-der-saturated with respect to calcite, resulting in dissolution of calcite cements, as consistent with microscopic dissolution features of the samples from this depth interval. Calcite dissolution results in formation of high secondary porosity and permeability, and is responsible for the superior quality of the reservoir rocks at this depth interval. These results illustrate the importance of pore water chemis-try in controlling carbonate precipitation/dissolution, which in turn controls porosity and permeability of oil and gas reservoir rocks in major sedimentary basins.  相似文献   

8.
南极洲万达盐湖为饱和方解石湖水。计算出的方解石饱和指数随水深增加而变化。在Ca2+及HCO3-活度值均一的上部氧化环境湖水中,pH及溶解氧(DO)是控制该变化的主要因素,在下部还原环境湖水中,Ca2+及HCO3-的活度对方解石的饱和指数SI的变化起主要作用。这充分揭示了湖底部近代沉积物中分布较多方解石矿物的原因。  相似文献   

9.
Data on the composition and content of plant pigments in water of the Cheboksary Reservoir collected in 1985–2005 are used to analyze the seasonal dynamics and spatial distribution of phytoplankton at different stages of reservoir life. A trophic burst could be distinctly seen in the reservoir in 1985, manifesting itself in exceedingly high (198 ± 41 μg/l) concentrations of photosynthetic pigment chlorophyll. In the process of ecosystem stabilization, chlorophyll concentration significantly dropped to vary from 8.2 ± 1.5 to 45.1 ± 21.0 μg/l in 1989–2005. The reservoir, located in a region subject to high anthropogenic load, has acquired the features of an eutrophic water body immediately after its creation and its trophic status remains unchanged all over its existence.  相似文献   

10.
Results of a special experiment conducted in the summer of 2002 in the Central pool of the Mozhaisk Reservoir are discussed. The experiment was aimed at studying short-period and small-scale variations in water temperature, electric conductivity, transparency, dissolved oxygen content, total and mineral phosphorus, phyto-, microzoo- and zooplankton. Statistical characteristics of the above-mentioned environmental parameters are presented.__________Translated from Vodnye Resursy, Vol. 32, No. 3, 2005, pp. 352–360.Original Russian Text Copyright © 2005 by Datsenko, Edelshtein, Goncharov, Puklakov, Chernega.  相似文献   

11.
Alpine/subalpine basins may exhibit substantial variability in solute fluxes despite many apparent similarities in basin characteristics. An evaluation of controls on spatial patterns in solute fluxes may allow development of predictive tools for assessing basin sensitivity to outside perturbations such as climate change or deposition of atmospheric pollutants. Relationships between basin physical characteristics, determined from geographical information system (GIS) tools, and solute fluxes and mineral weathering rates were explored for nine alpine/subalpine basins in Rocky Mountain National Park, Colorado, using correlation analyses for 1993 and 1994 data. Stream‐water nitrate fluxes were correlated positively with basin characteristics associated with the talus environment; i.e., the fractional amounts of steep slopes (≥ 30°), unvegetated terrain and young debris (primarily Holocene till) in the basins, and were correlated negatively with fractional amounts of subalpine meadow terrain. Correlations with nitrate indicate the importance of the talus environment in promoting nitrate flux and the mitigating effect of areas with established vegetation, such as subalpine meadows. Total mineral weathering rates for the basins ranged from about 300 to 600 mol ha?1 year?1. Oligoclase weathering accounted for 30 to 73% of the total mineral weathering flux, and was positively correlated with the amount of old debris (primarily Pleistocene glacial till) in the basins. Although calcite is found in trace amounts in bedrock, calcite weathering accounted for up to 44% of the total mineral weathering flux. Calcite was strongly correlated with steep slope, unvegetated terrain, and young debris—probably because physical weathering in steep‐gradient areas exposes fresh mineral surfaces that contain calcite for chemical weathering. Oligoclase and calcite weathering are the dominant sources of alkalinity in the basins. However, atmospherically deposited acids consume much of the alkalinity generated by weathering of calcite and other minerals in the talus environment. Published in 2001 by John Wiley & Sons, Ltd.  相似文献   

12.
Thermal waters of the Ömer–Gecek geothermal field, Turkey, with temperatures ranging from 32 to 92°C vary in chemical composition and TDS contents. They are generally enriched in Na–Cl–HCO3 and suggest deep water circulation. Silica and cation geothermometers applied to the Ömer–Gecek thermal waters yield reservoir temperatures of 75–155°C. The enthalpy–chloride mixing model, which approximates a reservoir temperature of 125°C for the Ömer–Gecek field, accounts for the diversity in the chemical composition and temperature of the waters by a combination of processes including boiling and conductive cooling of deep thermal water and mixing of the deep thermal water with cold water. It is also determined that the solubility of silica in most of the waters is controlled by the chalcedony phase. Equilibrium states of the Ömer–Gecek thermal waters studied by means of the Na–K–Mg triangular diagram, Na–K–Mg–Ca diagram, K–Mg–Ca geoindicator diagram, activity diagrams in the systems composed of Na2O–CaO–K2O–Al2O3–SiO2–CO2–H2O phases, log SI diagrams, and finally the alteration mineralogy indicate that most of the spring and low-temperature well waters in the area can be classified as shallow or mixed waters which are likely to be equilibrated with calcite, chalcedony and kaolinite at predicted temperature ranges similar to those calculated from the chemical geothermometers. It was also observed that mineral equilibrium in the Ömer–Gecek waters is largely controlled by CO2 concentrations.  相似文献   

13.
Methods of systems analysis and mathematical modeling are used to generalize hydrological, hydrochemical, and hydrobiological observational data with the aim to study the biohydrochemical conditions of organic and biogenic substance transformations in eight water areas in the White Sea. A hydroecological model describing transformations of N, P, and Si compounds and dissolved organic C, as well as the regime of O2 was used as a means of the study. Water exchange between water areas was evaluated using a hydrodynamic model. Averaged data on annual variations in water temperature, illumination, and transparency, as well as run-off characteristics (water flow in river mouths and organic and biogenic matter concentrations in the river water entering the sea) were used to calculate the dynamics of organic and mineral compounds of nutrients in different areas of the sea. The principal attention is paid to the verification of the model against field observational data, assessment of the biomass development conditions of aquatic animals, analysis of model results regarding the turnover time of organic and mineral components, and the evaluation of balances of organic dissolved and particulate N and P forms.__________Translated from Vodnye Resursy, Vol. 32, No. 4, 2005, pp. 435–451.Original Russian Text Copyright © 2005 by Leonov, Filatov, Chicherina.  相似文献   

14.
Isotopic compositions were determined for hydrothermal quartz, calcite, and siderite from core samples of the Newberry 2 drill hole, Oregon. The δ15O values for these minerals decrease with increasing temperatures. The values indicate that these hydrothermal minerals precipitated in isotopic equilibrium with water currently present in the reservoirs. The δ18O values of quartz and calcite from the andesite and basalt flows (700–932 m) have isotopic values which require that the equilibrated water δ18O values increase slightly (− 11.3 to −9.2‰) with increasing measured temperatures (150–265°C). The lithic tuffs and brecciated lava flows (300–700 m) contain widespread siderite. Calculated oxygen isotopic compositions of waters in equilibrium with siderite generally increase with increasing temperatures (76–100°C). The δ18O values of siderite probably result from precipitation in water produced by mixing various amounts of the deep hydrothermal water (− 10.5 ‰) with meteoric water (− 15.5 ‰) recharged within the caldera. The δ13C values of calcite and siderite decrease with increasing temperatures and show that these minerals precipitated in isotopic equilibrium with CO2 of about −8 ‰.The δ18O values of weakly altered (<5% alteration of plagioclase) whole-rock samples decrease with increasing temperatures above 100°C, indicating that exchange between water and rock is kinetically controlled. The water/rock mass ratios decrease with decreasing temperatures. The δ18O values of rocks from the bottom of Newberry 2 show about 40% isotopic exchange with the reservoir water.The calculated δ18O and δD values of bottom hole water determined from the fluid produced during the 20 hour flow test are −10.2 and −109‰, respectively. The δD value of the hydrothermal water indicates recharge from outside the caldera.  相似文献   

15.
Species composition, relative abundance and life history of unionid mussels are compared between 1982–86 and 1915–19 in Lake Hallwil and the outflowing brook. The recent samples of unionid mussels were collected by divers, whereas the older ones were from a shell collection. The motivation for the comparison was that the trophic degree of the lake has changed since the beginning of the century from mesotrophic to highly eutrophic. The effects of this increased trophic degree of the lake on the life cycle of unionid mussels is discussed. Predictions are made about species composition and life history in the context of the ongoing lake restoration by the authorities.  相似文献   

16.
南极洲万达盐湖为饱和方解石湖水。计算出的方解石饱和指数随水深增加而变化。在Ca~(2+)及HCO_3~-活度值均一的上部氧化环境湖水中,pH及溶解氧(DO)是控制该变化的主要因素,在下部还原环境湖水中,Ca~(2+)及HCO_3~-的活度对方解石的饱和指数SI的变化起主要作用。这充分揭示了湖底部近代沉积物中分布较多方解石矿物的原因。  相似文献   

17.
A rhyolitic ash-flow tuff in a hydrothermally active area within the Yellowstone caldera was drilled in 1967, and cores were studied to determine the nature and distribution of primary and secondary mineral phases. The rocks have undergone a complex history of crystallization and hydrothermal alteration since their emplacement 600,000 years ago. During cooling from magmatic temperatures, the glassy groundmass underwent either devitrification to alkali feldspar + α-cristobalite ± tridymite or granophyric crystallization to alkali feldspar + quartz. Associated with the zones of granophyric crystallization are prismatic quartz crystals in cavities similar to those termed miarolitic in plutonic rocks. Vapor-phase alkali feldspar, tridymite, magnetite, and sporadic α-cristobalite were deposited in cavities and in void spaces of pumice fragments. Subsequently, some of the vapor-phase alkali feldspar crystals were replaced by microcrystalline quartz, and the vapor-phase minerals were frosted by a coating of saccharoidal quartz.Hydrothermal minerals occur primarily as linings and fillings of cavities and fractures and as altered mafic phenocrysts. Chalcedony is the dominant mineral related to the present hydrothermal regime and occurs as microcrystalline material mixed with various amounts of hematite and goethite. The chalcedony displays intricate layering and was apparently deposited as opal from silica-rich water. Hematite and goethite also replace both mafic phenocrysts and vapor-phase magnetite. Other conspicuous hydrothermal minerals include montmorillonite, pyrite, mordenite, calcite, and fluorite. Clinoptilolite, erionite, illite, kaolinite, and manganese oxides are sporadic. The hydrothermal minerals show little correlation with temperature, but bladed calcite is restricted to a zone of boiling in the tuff and clearly was deposited when CO2 was lost during boiling.Fractures and breccias filled with chalcedony are common throughout Y-5 and may have been produced by rapid disruption of rock caused by sudden decrease of fluid pressure in fractures, most likely a result of fracturing during resurgent doming in this part of the Yellowstone caldera. The chalcedony probably was deposited as opal or β-cristobalite from a pre-existing silica floc that moved rapidly into the fractures and breccias immediately after the sudden pressure drop.  相似文献   

18.
李正魁  濮培民 《湖泊科学》2000,12(4):321-326
本文依据太湖秋冬季水体氮污染的特点,应用辐射增殖氮循环细胞进行了净化湖水氮污染的动态模拟实验,研究结果表明,富营养化湖水经固定化氮循环净化后,总氮下降７２．４％,氨氮下降８５．６％,出水水质得到明显改善,固定化氮循环细茵在冬季低温（７℃）条件下仍保持了较高的降氮能力,总氮和氨氮去除率分别为５５．６％,５８．９％,降氮效果与湖水滞留时间有关,探讨了固定化氮循环细茵的降氮机理。  相似文献   

19.
Thermal springs associated with normal faults in Utah have been analyzed for major cations and anions, and oxygen and hydrogen isotopes. Springs with measured temperatures averaging greater than 40°C are characterized by Na + K- and SO4 + Cl-rich waters containing 103 to 104 mg/l of dissolved solids. Lower temperature springs, averaging less than 40°C, are more enriched in Ca + Mg relative to Na + K. Chemical variations monitored through time in selected thermal springs are probably produced by mixing with non-thermal waters. During the summer months at times of maximum flow, selected hot springs exhibit their highest temperatures and maximum enrichments in most chemical constituents.Cation ratios and silica concentrations remain relatively constant through time for selected Utah thermal springs assuring the applicability of the geothermometer calculations regardless of the time of year. Geothermometer calculations utilizing either the quartz (no steam loss), chalcedony or Mg-corrected Na/K/Ca methods indicate that most thermal springs in Utah associated with normal faults have subsurface temperatures in the range of 25 to less than 120°C. This temperature range suggests fluid circulation is restricted to depths less than about three kilometers assuming an average thermal gradient of about 40°C/km.Thermodynamic calculations suggest that most thermal springs are oversaturated with respect to calcite, quartz, pyrophyllite, (Fe, Mg)-montmorillonite, microcline and hematite, and undersaturated with respect to anhydrite, gypsum, fluorite and anorthite. Chalcedony and cristobalite appear to be the only phases consistently at or near saturation in most waters. Theoretical evaluation of mixing on mineral saturation trends indicates that anhydrite and calcite become increasingly more undersaturated as cold, dilute groundwater mixes with a hot (150°C), NaCl-rich fluid. The evolution of these thermal waters issuing from faults appears to be one involving the dissolution of silicates such as feldspars and micas by CO2-enriched groundwaters that become more reactive with increasing temperature and/or time. Solution compositions plotted on mineral equilibrium diagrams trend from product phases such as kaolinite or montmorillonite toward reactant phases dominated by alkali feldspars.Isotopic compositions indicate that these springs are of local surface origin, either meteoric (low TDS, < 5000 mg/l) or connate ground water (high TDS, > 5000 mg/l). Deviations from the meteoric water line are the result of rock-water isotopic exchange, mixing or evaporation. Fluid source regions and residence times of selected thermal spring systems (Red Hill, Thermo) have been evaluated through the use of a σ D-contour map of central and western Utah. Ages for waters in these areas range from about 13 years to over 500 years. These estimates are comparable to those made for low-temperature hydrothermal systems in Iceland.  相似文献   

20.
The Feldberger Haussee, a highly eutrophic stratified hard-water lake located in the eastern part of Germany's Baltic lake district, was selected for a restoration programme combining external nutrient loading reduction and long-term biomanipulation. In 1980 the external phosphorus loading (1.8 g TP m−2 a−1) decreased by 90%, but water quality did not improve significantly within the following 6 years. In 1985 biomanipulation was initiated, with manual removal of cyprinid fish coupled with piscivore introductions as the principal measures. The expected changes in the pelagic community and improvements of water quality occurred after a delay of several years. Despite intensive manual removal of cyprinids and stocking of piscivores, standing stocks of cyprinid fish remained relatively high (130-260 kg ww ha−1) after some years of decline. Compared to the pre-biomanipulation period, mean seasonal (May-September) Daphnia spp. biomass roughly doubled (0.037 g C m−3vs. 0.084 g C m−3). However, the predominance of small (<1 mm) D. cucullata throughout the whole investigation period indicated that planktivory was still substantial. Paired observations between edible phytoplankton biomass and Daphnia spp. indicated that a significant decline in algal stocks would only occur if herbivorous biomass was above a certain threshold (0.2 g C m−3). Reduced external and internal loading in concert with pelagic calcite precipitation were most likely responsible for the decline in lake phosphorus concentrations, thereby substantially improving the water quality of Feldberger Haussee. Although this is not supported by quantitative evidence, we hypothesize that resource-related water quality improvements were caused by changes in the structure of the pelagic community leading to increased calcite precipitation. In agreement with the results of other investigations, we conclude that because stabilising mechanisms such as macrophyte growth were lacking in Feldberger Haussee, biomanipulation in stratified lakes may not be as successful as has been observed in shallow lakes. However, in hard-water lakes, calcite precipitation may act as another stabilising resource-related mechanism. Phosphorus associated with sedimenting calcite particles is insensitive to redox-conditions and may therefore not be re-mobilised from lake sediments even if hypolimnetic oxygen is depleted.  相似文献   

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