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1.
Many cities around the world are developed at alluvial fans. With economic and industrial development and increase in population, quality and quantity of groundwater are often damaged by over-exploitation in these areas. In order to realistically assess these groundwater resources and their sustainability, it is vital to understand the recharge sources and hydrogeochemical evolution of groundwater in alluvial fans. In March 2006, groundwater and surface water were sampled for major element analysis and stable isotope (oxygen-18 and deuterium) compositions in Xinxiang, which is located at a complex alluvial fan system composed of a mountainous area, Taihang Mt. alluvial fan and Yellow River alluvial fan. In the Taihang mountainous area, the groundwater was recharged by precipitation and was characterized by Ca–HCO3 type water with depleted δ18O and δD (mean value of −8.8‰ δ18O). Along the flow path from the mountainous area to Taihang Mt. alluvial fan, the groundwater became geochemically complex (Ca–Na–Mg–HCO3–Cl–SO4 type), and heavier δ18O and δD were observed (around −8‰ δ18O). Before the surface water with mean δ18O of −8.7‰ recharged to groundwater, it underwent isotopic enrichment in Taihang Mt. alluvial fan. Chemical mixture and ion exchange are expected to be responsible for the chemical evolution of groundwater in Yellow River alluvial fan. Transferred water from the Yellow River is the main source of the groundwater in the Yellow River alluvial fan in the south of the study area, and stable isotopic compositions of the groundwater (mean value of −8.8‰ δ18O) were similar to those of transferred water (−8.9‰), increasing from the southern boundary of the study area to the distal end of the fan. The groundwater underwent chemical evolution from Ca–HCO3, Na–HCO3, to Na–SO4. A conceptual model, integrating stiff diagrams, is used to describe the spatial variation of recharge sources, chemical evolution, and groundwater flow paths in the complex alluvial fan aquifer system.  相似文献   
2.
The aim of this research project is to identify, characterize and quantify natural attenuation (NA) processes in groundwater affected by emissions of abandoned waste disposal sites in Berlin-Kladow/Gatow, Germany. It is part of the funding priority called KORA established by the Federal Ministry for Education and Research (BMBF) to explore the extent to which NA can be used for remedial purposes for varied forms of soil and groundwater contamination. Information on the emission behaviour of individual parameters is generated on the basis of hydrogeochemical comparison of 20 years old and new data. Using groundwater-modelling and CFC-analysis, information on the transport and retention of pollutants in groundwater is compiled. The microbial colonization of contaminated aquifers is characterized by molecular biological methods [polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE)] to differentiate between contaminated and not contaminated zones.  相似文献   
3.
With the aim of contributing to the knowledge of the geochemical behaviour and mobility of the rare earth element (REE) in the natural water systems, the ground and surface waters of the Ottana-Orani area (Central Sardinia, Italy) were sampled. The study area consists of albititic bodies included in Hercynian granodiorites. The waters have pH in the range of 6.0-8.6, total dissolved solid (TDS) of between 0.1 and 0.6 g/l, and major cation composition dominated by Ca and Na, whereas predominant anions are Cl and/or HCO3.The pH and the major-element composition of the waters are the factors affecting the concentration of REE in solution. The concentrations of ∑REE+Y in the samples filtered at 0.4 μm vary between 140 and 1600 ng/l, with La of between 14 and 314 ng/l, and Yb of between <6 and 12 ng/l. A negative Ce anomaly, especially marked at high pH, is observed in the groundwaters. The surface waters show lower REE concentrations, which are independent of pH, and negligible Ce anomaly.Speciation calculations, carried out with the EQ3NR computer program, showed that the complexes with the CO32− ligand are the dominant REE species at pH in the range of 6.7-8.6. The REE3+ ions dominate the speciation at pH <6.7 and only in the light REE (LREE).The relative concentrations of REE in water roughly reflect those in the aquifer host rocks. However, when concentrations of REE in water are normalised relative to the parent rocks, a preferential fractionation of heavy REE (HREE) into the water phase can be observed, suggesting the greater mobility and stability of HREE in aqueous solution.  相似文献   
4.
四川盆地西部宫钾卤水以深层卤水形式赋存于地下4000余m的中三叠统雷口坡组四段(T2l4)盐系的碳酸盐岩储层中。富钾卤水与海水不同浓缩阶段相比,其中含K+含量异常高,构成液态钾矿资源;Br-、I-、B(3+)、Li+等稀有组分也远超过综合利用工业品位,为优质化工原料水。富钾卤水为沉积变质和钾盐溶滤的复合成因,具有固夜态找钾的指示意义。本文为四川盆地固液态找钾提供了有价值的线索。  相似文献   
5.
Multi-isotope (H, O, S, Sr, Pb) systems coupled with conventional (major and trace element) hydrogeochemical analysis were applied to determine the origin of water, to model water-rock-tailings interactions and for source apportionment of sulfur and associated toxic metals in the mining region of Taxco, Guerrero in southern Mexico. Oxygen and H isotopes indicate that meteoric water in the zone is rainwater undergoing varying degrees of isotopic fractionation by atmospheric evaporation whereas Sr isotopes trace the interaction of pristine water from volcanics of the regional recharge zone and subsequently flowing through sandstone and shale to spring points. Leachates form from two distinctive sources (spring water and surface water) having differential interactions with bedrocks prior to entering the tailings. Compared to pristine water, leachates are enriched in sulfate, metals (e.g. Fe, Mn, Pb and Zn) and metalloids (e.g. As). The sulfur isotopic composition of ore-sulfides, leachates, secondary precipitates, regional surface water and hypogenic sulfates is described in terms of a two-component mixing model with shale of Mexcala and limestone of Morelos formations representing the light and heavy end-members, respectively, whereas Sr isotopic composition is bracketed combining three lithogenic (Mexcala/Morelos, Tilzapotla and Taxco Schist) sources. Finally, leachates have a mixture of lead from ore-sulfides and Taxco Schist Formation (Family I) or from ore-sulfides alone (Family II). The application of multiple environmental isotopic techniques is an outstanding tool for elucidating complex interactions of water with bedrocks and tailings and for determining the source of sulfur and toxic metal from mining and other metal polluted environments.  相似文献   
6.
PHREEQC在研究地浸溶质迁移过程中的应用   总被引:5,自引:1,他引:5  
应用地球化学模式PHREEQC,揭示地浸过程中溶质迁移的存在形式及各种形式之间的转化关系。通过计算饱和指数,确定溶质水解沉淀的水文地球化学条件临界值。  相似文献   
7.
A conceptual model with water samples from ten geothermal fields (?smil, Ilg?n (Çavu?cugöl), Tuzlukçu-Ak?ehir, Seydi?ehir and Kavakköy, Hüyük, Ere?li-Akhüyük, Kad?nhan?, Cihanbeyli, Karap?nar and Bey?ehir) in the province of Konya defined the geothermal system. Carbonates, quartzite and marbles of Paleozoic metamorphics are the reservoir rocks and the heating sources are igneous rock intrusions and geothermal gradient. The variable thermal water (CaMgHCO3, CaSO4, NaSO4, CaHCO3, CaNaHCO3, NaCl and CaNaClHCO3) had EC and temperature between 177.8 and 56,100 μS/cm and between 18.3 and 44 °C, respectively. Ca2+ in geothermal fluids are associated with marble and carbonate rocks and the high chloride shows direct connection with deep geothermal system, and prolonged contact with evaporite rocks. Sulphate originates from dissolution of and oxidation of sulphate and sulphur-bearing minerals. The high As, B, F and Mn concentration in some thermal water samples were determined as 85 μg/l, 148.56 mg/l, 3.01 mg/l and 208.13 mg/l, respectively. Reservoir temperatures computed by Na/K geothermometers were between 85.37–158.89 °C for Ak?ehir thermal waters and 58.78–90.45 °C for Ere?li thermal waters. The maximum reservoir temperature of other geothermal waters was 75 °C by the silica geothermometers.  相似文献   
8.
9.
本文以大庆西部地区地下水含氟量的分布规律为例,较全面地论述了氟的来源、富集的水文地球化学环境,并应用热力学公式计算了氟在地下水中各存在形式的分配分数。  相似文献   
10.
Groundwater is a critical resource in Khanyounis city as it is the main source of water. The aquifer has deteriorated to a high degree, during the last two to three decades, in quality and quantity. More than 90% of the population get their drinking water from brackish water desalination plants. Fifteen domestic wells were sampled in 2002 to probe the hydrogeochemical components that influence the water quality. Na, K, Ca, Mg, Cl, SO4, NO3, and HCO3 were analyzed. The data were statistically treated and plotted on the Piper diagram. A hydrogeochemical numerical model for carbonate minerals was constructed using the PHREEQ package. The results show that the groundwater is polluted with Cl, from seawater, and NO3, sourced from fertilizers and sewage. The regression analysis shows that there are three groups of elements that are significantly and positively correlated. Na–Cl signature and plot show that seawater intrusion is advancing into the aquifer. The main hydrochemical facies of the aquifer (Na+K–Cl+SO4), represents 60% of the total wells. Whereas 32.3% of the wells are located in the no pair up and no pair down fields on the Piper diagram. Calcite, dolomite, and aragonite solubility were assessed in terms of the saturation index where they show positive values indicating supersaturation. The hydrogeochemical behavior is rather complicated and is affected by anthropogenic and natural parameters.  相似文献   
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