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This paper describes the hydrological changes caused by inter‐basin water transfer and the reservoir development on the hydrological regimes of two rivers. The Sabljaki Reservoir in the Zagorska Mre?nica River and the Bukovik Reservoir in the upper Dobra River began operation in 1959. Both are part of the hydroelectric power plant (HEPP) Gojak, whose installed capacity is 50 m3/s. Their water volumes at the spillway altitudes of 320·10 and 320·15 m a. s. l. are 3·3 × 106 and 0·24 × 106 m3 respectively. Both the Dobra and Mre?nica Rivers are losing, sinking and underground karst rivers. A 9376‐m‐long tunnel provides water from the Sabljaki Reservoir to the HEPP Gojak, which was constructed in the Lower Dobra River. The Sabljaki Reservoir is located in the Pla?ki karst polje, while the Bukovik Reservoir is located in the neighbouring Ogulin karst polje. The consequences of the inter‐basin water transfer are strong and have caused abrupt changes in the hydrological regimes of the downstream sections of both rivers. At the same time, the construction and development of both the reservoirs have also caused hydrological changes to the upstream section of the Upper Dobra River. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
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Molybdenum concentrations in Icelandic geothermal waters lie in the range 1–70 ppb. Warm waters and dilute high-temperature waters which contain high concentrations of sulphide are lowest in molybdenum. No correlation is otherwise observed between molybdenum concentrations and temperature. Surface waters and cold ground waters do not contain detectable molybdenum (<1 ppb). It seems likely that leaching rate is the prime factor in limiting molybdenum levels in these waters. Within individual geothermal fields molybdenum concentrations are either approximately constant or they vary regularly across the field. This regular variation may often be correlated with variations in other solute concentrations and subsurface temperatures and is taken to indicate a control of molybdenum mobility by a temperature dependent equilibrium. The evidence suggests that the solubility of molybdenite is responsible. Molybdenite has not been found in active geothermal systems in Iceland but is known to occur in some New Zealand geothermal systems and it has been identified in hydrothermally altered Tertiary basalt formations at Reydarártindur in southeast Iceland. Boiling and mixing with cold water leads to molybdenite undersaturation and thus these processes favour leaching of molybdenum from the rock. On the other hand, conductive cooling leads to supersaturation which favours removal of molybdenum from solution. 相似文献
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Stefán Arnórsson 《Geochimica et cosmochimica acta》1984,48(12):2489-2502
Germanium concentrations in geothermal waters in Iceland lie mostly in the range 2–30 ppb. There is an overall positive relation between the germanium content of the water and its temperature. Most of the germanium occurs as Ge(OH)?5in solution but Ge(OH)4 may also be present in significant amounts in saline waters when above 200°C. Evidence indicates that aqueous germanium concentrations are controlled by exchange reactions where it substitutes for silica in silicates and iron in sulphides. It is the rate of dissolution and the relative abundance of the alteration minerals which take up germanium to a variable extent that ultimately fix Ge(OH)4 concentrations in the water. This, together with water pH, fixes total dissolved germanium. It is mostly the primary rock composition that dictates the relative abundance of the alteration minerals. Conductive cooling in upflow zones favours removal of germanium from solution. During the initial stages of boiling of rising hot water dissolution is enhanced but precipitation at later stages.Thermodynamic data of various aqueous germanium species and several minerals are summarized and dissociation constants and solubilities estimated at elevated temperatures using available predictive methods. 相似文献
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Kristín Vala Ragnarsdóttir John V Walther Stefán Arnórsson 《Geochimica et cosmochimica acta》1984,48(7):1535-1553
The bulk composition and mineralogy of hydrothermally altered tholeiite, along with the composition and speciation of fluid, have been determined for a well-defined alteration zone at 240°C and 110 bars at Svartsengi, Iceland. Mass balances between the geothermal fluid and altered tholeiite, relative to a seawater/fresh water mixture and unaltered tholeiite, indicate the overall reaction per 1000 cm3 is: 1325 gm plagioclase + 1228 gm pyroxene + 215 gm oxide-minerals break down to form 685 gm chlorite + 636 gm albite + 441 gm quartz + 249 gm epidote + 266 gm calcite + 201 gm oxide-minerals + 15 gm pyrite, requiring an influx of 123 gm CO2, 10 gm H2S and 4 gm Na2O and a release of 57 gm SiO2, 35 gm FeO, 21 gm CaO, 8 gm MgO and 4 gm K2O.Principal reactions, deduced from textural evidence, include Na-Ca exchange in plagioclase, precipitation of quartz, calcite and anhydrite, and formation of chlorite and epidote by reactions between groundmass minerals and fluid.Thermodynamic analyses of authigenic minerals and downhole fluid indicate that the fluid maintains a state close to equilibrium with the secondary mineral phases chlorite, epidote, albite, quartz, calcite, prehnite, anhydrite, pyrite and magnetite, whereas remnant primary labradorite and augite are out of equilibrium with the fluid.Water/rock ratios for the system are determined under a variety of assumptions. However, the open nature of the system makes comparisons with experimental and theoretical closed system studies ambiguous. 相似文献
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Stefán Arnórsson Einar Gunnlaugsson Hördur Svavarsson 《Geochimica et cosmochimica acta》1983,47(3):567-577
New data from geothermal wells in Iceland have permitted empirical calibration of the chalcedony and geothermometers in the range of 25–180°C and 25–250°C respectively. The temperature functions are: Concentrations are expressed in ppm. These temperature functions correspond well with the chalcedony solubility data of Fournier (1973) and the thermodynamic data for low-albite/microcline/solution equilibria of Heloeson (1969).A new CO2 geothermometer is proposed which is considered to be useful in estimating underground temperatures in fumarolic geothermal fields. Its application involves analysis of CO2 concentrations in the fumarole steam. The temperature function which applies in the range 180?300°C is: logCO2 = 37.43 + 73192/T- 11829· 103/T2 + 0.18923T- 86.187·logT where T is in °K and CO2 in moles per kg of steam. 相似文献
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This paper is an attempt to contribute to the improvement of an analysis model within overall structural synthesis procedure for the multi-deck ships. The paper is organized in two parts: modeling principles and model validation. Principles of the proposed generic model formulation on the global and sub-structure levels are given in detail while the load model is briefly summarized. The basic building blocks (macro-elements and gross-elements) for the modeling of ordinary stiffened panels, combining numerical and analytical approaches, are presented and discussed w.r.t. requirements for a multi-deck structure. Different surrogates (sets of elements and ordinary macro-elements) used for equivalent modeling of large side openings are evaluated, since the reduced shear stiffness of superstructure sides has large influence on the hull girder stress distributions along the entire cross section height. The generic ship models developed using outlined principles and the basic building blocks are further validated through complex examples of a large cruise ship and a livestock carrier. On the global level, the accuracy of the generic model w.r.t. the longitudinal stress distribution over ships height is compared with a standard full ship FE model. The results confirmed that the suggested structural modeling principles, based on the generic FE model can be applied for the fast investigation of different structural topological/geometrical concepts as well as for the ordinary scantling/material optimization. 相似文献
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The speciation of aqueous dissolved sulfur was determined in hydrothermal waters in Iceland. The waters sampled included hot springs, acid-sulfate pools and mud pots, sub-boiling well discharges and two-phase wells. The water temperatures ranged from 4 to 210 °C, the pHT was between 2.20 and 9.30 at the discharge temperature and the SO4 and Cl concentrations were 0.020-52.7 and <0.01-10.0 mmol kg−1, respectively. The analyses were carried out on-site within ∼10 min of sampling using ion chromatography (IC) for sulfate (SO42−), thiosulfate (S2O32−) and polythionates (SxO62−) and titration and/or colorimetry for total dissolved sulfide (S2−). Sulfite (SO32−) could also be determined in a few cases using IC. Alternatively, for few samples in remote locations the sulfur oxyanions were stabilized on a resin on site following elution and analysis by IC in the laboratory. Dissolved sulfate and with few exceptions also S2− were detected in all samples with concentrations of 0.02-52.7 mmol kg−1 and <1-4100 μmol kg−1, respectively. Thiosulfate was detected in 49 samples of the 73 analyzed with concentrations in the range of <1-394 μmol kg−1 (S-equivalents). Sulfite was detected in few samples with concentrations in the range of <1-3 μmol kg−1. Thiosulfate and SO32− were not detected in <100 °C well waters and S2O32− was observed only at low concentrations (<1-8 μmol kg−1) in ∼200 °C well waters. In alkaline and neutral pH hot springs, S2O32− was present in significant concentrations sometimes corresponding to up to 23% of total dissolved sulfur (STOT). In steam-heated acid-sulfate waters, S2O32− was not a significant sulfur species. The results demonstrate that S2O32− and SO32− do not occur in the deeper parts of <150 °C hydrothermal systems and only in trace concentrations in ∼200-300 °C systems. Upon ascent to the surface and mixing with oxygenated ground and surface waters and/or dissolution of atmospheric O2, S2− is degassed and oxidized to SO32− and S2O32− and eventually to SO42− at pH >8. In near-neutral hydrothermal waters the oxidation of S2− and the interaction of S2− and S0 resulting in the formation of Sx2− are considered important. At lower pH values the reactions seemed to proceed relatively rapidly to SO42− and the sulfur chemistry of acid-sulfate pools was dominated by SO42−, which corresponded to >99% of STOT. The results suggest that the aqueous speciation of sulfur in natural hydrothermal waters is dynamic and both kinetically and source-controlled and cannot be estimated from thermodynamic speciation calculations. 相似文献
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West Java in the western part of the Sunda Arc has a relatively high seismicity due to subduction activity and faults. In this study, double-difference tomography was used to obtain the 3D velocity tomograms of P and S waves beneath the western part of Java. To infer the geometry of the structure beneath the study area, precise earthquake hypocenter determination was first performed before tomographic imaging. For this, earthquake waveform data were extracted from the regional Meteorological, Climatological, Geophysical Agency (BMKG) network of Indonesia from South Sumatra to Central Java. The P and S arrival times for about 1,000 events in the period April 2009 to July 2016 were selected, the key features being events of magnitude > 3, azimuthal gap < 210° and number of phases > 8. A nonlinear method using the oct-tree sampling algorithm from the NonLinLoc program was employed to determine the earthquake hypocenters. The hypocenter locations were then relocated using double-difference tomography (tomoDD). A significant reduction of travel-time (root mean square basis) and a better clustering of earthquakes were achieved which correlated well with the geological structure in West Java. Double-difference tomography was found to give a clear velocity structure, especially beneath the volcanic arc area, i.e., under Mt Anak Krakatau, Mt Salak and the mountains complex in the southern part of West Java. Low velocity anomalies for the P and S waves as well as the vP/vS ratio below the volcanoes indicated possible partial melting of the upper mantle which ascended from the subducted slab beneath the volcanic arc. 相似文献
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River basins in mountainous regions are characterized by strong variations in topography, vegetation, soils, climatic conditions and snow cover conditions, and all are strongly related to altitude. The high spatial variation needs to be considered when modelling hydrological processes in such catchments. A complex hydrological model, with a great potential to account for spatial variability, was developed and applied for the hourly simulation of evapotranspiration, soil moisture, water balance and the runoff components for the period 1993 and 1994 in 12 subcatchments of the alpine/pre‐alpine basin of the River Thur (area 1703 km2). The basin is located in the north‐east of the Swiss part of the Rhine Basin and has an elevation range from 350 to 2500 m a.s.l. A considerable part of the Thur Basin is high mountain area, some of it above the tree‐line and a great part of the basin is snow covered during the winter season. In the distributed hydrological model, the 12 sub‐basins of the Thur catchment were spatially subdivided into sub‐areas (hydrologically similar response units—HRUs or hydrotopes) using a GIS. Within the HRUs a hydrologically similar behaviour was assumed. Spatial interpolations of the meteorological input variables wereemployed for each altitudinal zone. The structure of the model components for snow accumulation and melt, interception, soil water storage and uptake by evapotranspiration, runoff generation and flow routing are briefly outlined. The results of the simulated potential evapotranspiration reflect the dominant role of altitudinal change in radiation and albedo of exposure, followed by the influence of slope. The actual evapotranspiration shows, in comparison with the potential evapotranspiration, a greater variability in the lower and medium altitudinal zones and a smaller variability in the upper elevation zones, which was associated with limitations of available moisture in soil and surface depression storages as well as with the evaporative demand of the local vegetation. The higher altitudinal dependency and variability of runoff results from the strong increase in precipitation and the decrease in evaporation with increased altitude. An increasing influence of snow cover on runoff as well as evapotranspiration with altitude is obvious. The computed actual evapotranspiration and runoff were evaluated against the observed values of a weighting lysimeter and against runoff hydrographs. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献