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71.
Peter Herzsprung Martin Schultze Bertram Boehrer Anja Duffek Andrea Van der Veen Kurt Friese 《Limnologica》2010,40(2):182-190
Between 1999 and 2002, a former open-cast mine was filled with river water forming the recent Lake Goitsche. During filling initially acid water was neutralised. Phosphorus (P) imported from Mulde River was nearly completely removed from the water column by co-precipitation with iron (Fe) and aluminium (Al) and deposited in the sediment.During extremely high waters of the Mulde River in 2002, a dike breach facilitated a second high import of P into Lake Goitsche with suspended and dissolved matter. The analysis of total phosphorus (TP), however, showed that P again had been eliminated from the water body a few months after the flood event. Sediment investigations before filling with river water, during filling, and after the flood event were used to analyse the process of P immobilisation in a lake with acid mine drainage history.The ratios of Fe to soluble reactive P (SRP) of sediment pore water were up to three orders of magnitudes higher than in natural lakes and can serve as an indicator for potential internal P loading from sediments. The SRP concentrations at the oxic/anoxic boundary were near or below the limit of quantification (< 0.2 μmol/L). Fe and manganese (Mn) redox cycling were responsible for hindering P dissolution from sediment to lake water.Finally it can be stated, that the risk of eutrophication for such a lake seems to be low. 相似文献
72.
山东莱芜接触交代—热液铁矿矿体形态研究 总被引:1,自引:0,他引:1
在对莱芜接触交代铁矿地质特征研究中发现以往地质报告在矿体连接上存在混乱,使矿体形态失真。为便于今后矿体对比和成矿规律的认识,提出了矿体形态分类原则,并以三分法对矿体形态进行分类。指出矿体产状变化是矿体膨胀收缩、分支复合和尖灭再现的结果。根据矿体形态分类指出了找矿方向。不同的矿体形态反映不同的控矿构造,反映不同的矿体规模,反映不同的成矿岩体形态产状。单斜缓倾矿体的成矿岩体是岩床,控矿较小;陡倾矿体和背向斜矿体的成矿岩体是岩盖,控矿较大。 相似文献
73.
74.
Lepidocrocite (γ‐FeOOH) nanoparticles were synthesized from iron(II) sulfate solution and characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform‐IR (FT‐IR), nitrogen adsorption, and point of zero charge pH (pHPZC) analyses. TEM, XRD, and FT‐IR analyses proved the synthesis of nano‐lepidocrocite. Surface area and pHPZC of the synthesized lepidocrocite were 68.1 m2 g?1 and 4.8, respectively. Utilization of the synthesized lepidocrocite in the adsorption of Lanacron brown S‐GL (LBS‐GL) from aqueous solutions was investigated, and the effect of lepidocrocite dosage, pH, temperature, and contact time on this process were optimized and modeled using response surface methodology approach. The lepidocrocite dosage of 0.015 g, pH 3.5, temperature of 38°C, and contact time of 100 min were determined as optimum adsorption conditions. Isotherm and kinetics of the adsorption process were analyzed at the optimum conditions. The equilibrium data were fitted well to the Langmuir isotherm model. The maximum monolayer adsorption capacity was 528.21 mg g?1. The adsorption process was described by the pseudo‐second‐order kinetic model. Furthermore, the effect of pH on the desorption of LBS‐GL was investigated. High LBS‐GL desorption efficiency was achieved at a high pH value. 相似文献
75.
河北滦平周台子条带状铁矿地质特征、围岩时代及其地质意义 总被引:5,自引:4,他引:1
河北滦平县周台子铁矿位于华北克拉通北缘,是产于前寒武纪单塔子群变质岩系中的鞍山式铁矿,具有条带状铁建造(BIF)特征。矿石主要呈条带状构造,有的呈条纹和致密块状构造。矿石类型主要以石英磁铁矿型为主,含铁介于30%~35%。前寒武纪变质岩是矿床的主要围岩,出露有黑云母(角闪)斜长片麻岩和斜长角闪岩,局部见花岗片麻岩。原岩恢复表明,黑云母(角闪)斜长片麻岩的原岩为英安岩-流纹岩,斜长角闪岩原岩为玄武岩。花岗片麻岩的SiO2含量大于56%,MgO含量小于3%,Al2O3含量大于15%,Sr含量大于500×10-6,Yb含量均小于1.9×10-6,轻重稀土元素分异明显,重稀土元素强烈亏损,并且Eu负异常不明显,表明该片麻岩具埃达克质岩石的地球化学特征。锆石U-Pb定年结果显示出几组年龄,分别是2512±21Ma, 2452±9.6Ma,2394±55Ma。大体看,2512Ma代表了火山喷发和周台子铁矿BIF沉淀年龄,2452Ma左右的锆石年龄代表了TTG质花岗片麻岩的侵位结晶年龄,2394Ma锆石年龄代表了周台子铁矿经历了一次变质作用,并对原有的岩石和矿石进行了改造。锆石Hf同位素特征显示斜长角闪岩和TTG质片麻岩的岩浆源区受到过古老地壳物质的混染。周台子铁矿构造环境可能是与裂谷有关的张性环境。 相似文献
76.
To improve the usefulness and accuracy of modeling Earth's anthrobiogeochemical metal cycles, global maps at approximately 1° × 1° are produced of the concentrations and masses of Fe, Al, Cu, and Zn contained in continental sediments and soils. The maps generated utilize inverse distance weighting (IDW) and cokriging to generate new estimates for geospatially weighted mean global concentrations for these metallic micronutrients. Sediment metal concentration maps are generated from IDW of sediment samples; global soil maps are produced via cokriging upon an underlying parent rock dataset composed of both surface bedrock and sediment samples. Derived are independent estimates for the global mean concentrations in continental sediments (Fe = 3.1 wt.%, Al = 6.1 wt.%, Cu = 45 μg/g, Zn = 86 μg/g) and soils (Fe = 2.5 wt.%, Al = 3.9 wt.%, Cu = 17 μg/g, Zn = 50 μg/g). While continental sediment concentrations for Cu are within the range of previous estimates, Zn concentrations are relatively higher, ~ 20 μg/g above previous estimates. Fe and Al are slightly depleted (~ 1 wt.%) in continental sediments relative to previous estimates, likely ascribable to sampling bias and error inherent in the comparative methodologies. Besides an estimated global mean, metal concentrations in soils are also broken down by FAO soil group. Metal masses in sediments and soils remain within 30% of previous, non-spatial estimates. These maps also illustrate the discernable spatial variability across the Earth's surface. Despite data gaps, maps of metal mass show regional patterns such as the high quantities of Al in the soils and biomass of the Amazonia and Congo regions. Concentrations of metals are relatively high in the anthrosols of China. Finally, this analysis highlights those areas for which generating and providing publically available geochemical data should be prioritized. For instance, gypsisols, lixisols, and nitisols have little to no analytical data available on metal contents. A sensitivity analysis suggests that the most poorly constrained soil metal concentrations occur in the thick, old tropical soils of central Africa and the anthrosols of eastern China. 相似文献
77.
78.
The influences of macronutrient enrichment on iron absorption, adsorption, and the bioconcentration factor (BCF) of iron by coastal diatoms were examined. In addition, the distribution of different iron size fractions in seawater in relation to two diatom species exposed to nutrient enrichment over an extended period (6 days for Thalassiosira weissflogii, and 4 days for Skeletonema costatum), was investigated. Iron concentrations were measured of seven size fractions: particles (>0.4 μm), colloidal particles (0.4 μm–100, 100–50, 50–30, 30–10, 10–3 kDa), and soluble species (<3 kDa).The absorption, adsorption, uptake, BCF of iron by the diatoms, and the iron species distribution in seawater were affected by the diatom species, as well as the nitrate (N) and phosphate (P) concentration. The addition of P could affect the iron internalization strategy. The content of soluble iron species was positively correlated with the amount of iron absorption by T. weissflogii, but it was not suitable for S. costatum. 相似文献
79.
80.
Liang-Saw Wen Peter H. Santschi Kent W. Warnken William Davison Hao Zhang Hsiu-Ping Li Kuo-Tung Jiann 《Estuarine, Coastal and Shelf Science》2011
It is generally assumed that estuarine mixing is continuous for metals from terrestrial sources, gradually decreasing towards the open ocean endmember. Here we show that, chemical reactivity, determined by ion exchange method, and molecular weight distributions, obtained using cross-flow ultrafiltration, of dissolved Cd, Cu, and Ni in the surface waters of the Gulf of Mexico varied systematically across the estuarine mixing zone of the Mississippi River. Most size or chemical affinity fractions of dissolved metals (<0.4 μm) were linearly related to salinity (10.8–36.6), suggesting that the distribution of these elements was mainly controlled by continuous mixing processes. Dissolved concentrations across the salinity gradient ranged for Cd: 87–187 pM; Cu: 1.4–18.3 nM; and Ni: 2.6–18.8 nM, with highest values near the Mississippi river mouth, and lowest concentrations in a warm core ring in the Gulf of Mexico. Dissolved Cd was mostly present as a truly dissolved (<10 kDa, 97 ± 1%) and cationic fraction (Chelex-100 extractable, 94 ± 4%). A novel observation across the estuarine mixing zone was that colloidal metal concentrations were identical to either inert (for Cu, Ni) or AMPG-labile anionic (Cu, Cd) fractions. The difference in behavior between Cu and the other two metals might indicate differences in the biopolymeric nature of the metal–organic chelates. In particular, the anionic-organic Cd fractions accounted for just 3 ± 1%, on average. However, for Cu, it was 24 ± 4%, and for Ni, it was 9 ± 6%. The fractions of the total dissolved metal fractions that were “inert” averaged 31 ± 10% for Cu and 29 ± 12% for Ni. Small but noticeable amounts (6 ± 3%) of dissolved inert Cd fractions were also present. Apparent non-local transport processes, likely associated with cross-shelf sediment resuspension processes, could have been responsible for the relatively high concentrations of ‘inert’ and ‘anionic’ metal fractions in high salinity coastal waters, and accounting for the persistence of metals bound to humic substances in the Gulf of Mexico. 相似文献