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101.
Gaseous nitric acid and ammonia were sampled with annular denuders at a forest savannah site from April to December 1987. The analysis of the extract was made spectrophotometrically and by a selective electrode for NO3
– and NH4
+, respectively. Higher concentrations were observed during the vegetation burning period at the end of the dry season. In the studied savannah area, large soil emissions of NO occur during the rainy season, although very low concentrations of HNO3 (0.035 ppb) and also of particulate NO3
– (0.43 g m-3) were observed; it is likely that NOx are lost by fast vertical transport to the upper troposphere. During the nonburning period, the average concentration of NH3 was 2.7 ppb, which is much lower than values given in the literature for the tropical America atmosphere. The concentrations of HNO3 and NH3 were always below the values needed to produce ammonium nitrate aerosols. 相似文献
102.
1999与 2 0 0 0年夏季对南极菲尔德斯半岛不同地点大气中 N2 O浓度进行了监测 ,分析了苔藓植被区 N2 O浓度季节变化特征 ;2 0 0 0年夏季该植被区 N2 O浓度均值为 ( 31 0 .7± 4.4)×1 0 - 9(体积百分比 ) ,比 1 999年的 ( 32 1 .9± 3.3)× 1 0 - 9约低 1 1× 1 0 - 9;阿德雷岛企鹅滩及其沙坝处N2 O浓度变化趋势与苔藓植被区相一致 ,浓度均值分别为 ( 31 2 .4± 5 .1 )× 1 0 - 9和 ( 31 2 .7± 5 .3)× 1 0 - 9,比 1 999年约低 9× 1 0 - 9;另外 ,不同地点大气中 N2 O浓度普遍比 1 999年低 ,但整体变化规律相似 :各考察站区 N2 O浓度普遍高于无人区 ;唯一例外的是企鹅聚集区 N2 O浓度却高于各考察站区 ,暗示了企鹅及其排泄物、人为源是南极大气中 N2 O主要的源。本文初步探讨了 N2 O浓度异常降低的原因 相似文献
103.
基于我国钴资源分布分散、且多为伴生、品位低的现状,对某铜钴矿化区钴矿石中的钴碳酸盐矿物、含钴铁氧化物和具有吸附态的粘土矿物进行了钴的赋存状态和浸取试验研究,查明了钴的赋存状态,并以此为依据,运用逐一条件试验和正交试验相互验证的办法,确定了最优化的浸取试验方案,该方法对此低品位氧化钴矿石中钴的浸出率达到90%以上。 相似文献
104.
T. H. Papenbrock F. Stuhl K. P. Müller J. Rudolph 《Journal of Atmospheric Chemistry》1992,15(3-4):369-379
A latitudinal profile (30° W, from 30° N to 30° S) of mixing ratios of nitric acid and particulate nitrate was determined on the Atlantic Ocean during the Polarstern cruise ANT VII/1 from Bremerhaven, Germany, to Rio Grande, Brazil. The detection of HNO3 was performed simultaneously by laser-photolysis fragment-fluorescence (LPFF) and by nylon filter packs. The detection limit was about 30 pptv for a signal accumulation time of 1 h for LPFF and about 5 pptv for the filters at a collection time of 4 h. In general, the mixing ratios of HNO3 in the Northern Hemisphere were found to be significantly higher than those in the Southern Hemisphere. The Atlantic background concentrations frequently varied between 80 pptv and the detection limit. Larger deviations from this trend were found for the more northern latitudes and for episodes like crossings of exhaust plumes from ships or from continental pollutions sources. 相似文献
105.
Immobilization of trace elements in contaminated soils by zero-valent iron (ZVI) is a promising remediation method, but questions about its long-term performance remain unanswered. To quantify immobilization and predict possible contaminant remobilization on long timescales detailed knowledge about immobilization mechanisms is needed. This study aimed at assessing the long-term effect of ZVI amendments on dissolved copper and arsenic in contaminated soils, at exploring the immobilization mechanism(s), and at setting up a geochemical model able to estimate dissolved copper and arsenic under different scenarios. Samples from untreated and ZVI-treated plots in two field experiments where ZVI had been added 6 and 15 years ago were investigated by a combination of batch experiments, geochemical modeling and extended X-ray absorption fine structure (EXAFS) spectroscopy. Dissolved copper and arsenic concentrations were described by a multisurface geochemical model with surface complexation reactions, verified by EXAFS. The ZVI remained “reactive” after 6–15 years, i.e. the dissolved concentrations of copper and arsenic were lower in the ZVI-treated than in the untreated soils. There was a shift in copper speciation from organic matter complexes in the untreated soil to surface complexes with iron (hydr)oxides in the ZVI-treated soil. The pH value was important for copper immobilization and ZVI did not have a stabilizing effect if pH was lower than about 6. Immobilization of arsenic was slightly pH-dependent and sensitive to the competition with phosphate. If phosphate was ignored in the modeling, the dissolution of arsenate was greatly underestimated. 相似文献
106.
The Effect of Organic Carbon-Iron Oxide Association on the Preservation of Sedimentary Organic Carbon in Marine Environments 总被引:1,自引:0,他引:1
Understanding the mechanisms responsible for long-term storage of organic carbon (OC) in marine environment is important for studying the marine carbon cycling and predicting how the global carbon cycle will respond to climate change. It is estimated that more than 20% of the OC in marine sediments is associated with iron oxides and thus these complexes are one of the most important factors in the long-term storage of OC. The OC-iron oxide (OC-Fe) association can be formed through either adsorption or co-precipitation, but the dominant mechanism of OC-Fe association in marine environments is co-precipitation. The combination of OC from different sources with iron oxides is selective. Iron oxides preferentially combine with marine OC in most marine environments, but in estuarine delta regions they prefer terrestrial OC. Due to large inputs of terrestrial materials, high primary production and frequent re-suspension, estuarine and marginal seas are suitable sites for OC-Fe association studies, which should be emphasized in the future. 相似文献
107.
Impact of trace metals on denitrification in estuarine sediments of the Douro River estuary,Portugal 总被引:1,自引:0,他引:1
Denitrification influences the nitrogen budget in estuaries by removing fixed nitrogen from the inorganic pool; rates are dependent on both geological and geographic conditions as well as increasing anthropogenic impacts. In this study the effects of copper (Cu), chromium (Cr), zinc (Zn), cadmium (Cd) and lead (Pb), on the denitrification pathway were evaluated in subtidal and intertidal sediments of the Douro River estuary. Dinitrogen, N2O and NO2− production rates were measured in triplicate slurries of field samples under different treatments of metal concentrations. Results demonstrated that similar metal amendments led to different site responses for denitrification, suggesting that variations in sediment properties (metal concentrations, grain size, organic matter content, etc.) and/or differences in denitrifying community tolerance modulate the level of metal toxicity. Denitrifying communities in subtidal muddy sediments were not affected by increasing concentrations of metals. In contrast, intertidal sandy sites revealed high sensitivity to almost all trace metals tested; almost complete inhibition by Cr (95%) and Cu (85%) was observed for 98 and 79 μg per gram of wet sediment respectively, and by Zn (92%) at the highest concentration added (490 μg per gram of wet sediment). Moreover, the addition of trace metals stimulated N2O and NO2− accumulation in intertidal sandy (Zn, Cu, Cr and Cd) and muddy sediments (Cu and Zn), demonstrating a pronounced inhibitory effect on specific steps within the denitrification enzymatic system. In summary, the results obtained suggest that, according to the type of estuarine sediment, trace metals cannot only reduce total N removal from an estuary via denitrification but also can enhance the release of N2O, a powerful greenhouse gas. 相似文献
108.
掺铝氧化锌厚膜制备及其对三甲胺和海产品鲜度的敏感性 总被引:2,自引:0,他引:2
用烧结法制备掺铝氧化锌厚膜,把氧化锌粉末分别同0%,1%,3%,5%的Al2O3粉末机械研磨混合均匀,在1100℃下烧3h,再同粘合剂,有机溶剂混合制成浆料,用刮刀法在氧化铝基片上浆料制成膜,在100℃下烘干后再经1100℃烧结2h。膜的灵敏度的测量方法是将膜放在玻璃管内加热到测量温度,测量膜暴露在一定浓度TMA气体或由牡蛎放出的气体时电阻值的变化。测量温度为200,250,300℃和400℃,T 相似文献
109.
详细地研究了硼在水合氧化锆吸附剂上的吸附行为。研究结果表明,水合氧化锆的吸硼速率较快,2h可完全达平衡,且吸附可用Freundlich等温吸附线很好地拟合。被吸附的硼易被碱液洗脱,通过水合氧化锆上硼的“吸附-脱附循环”研究,表明该吸附剂的吸附性能好,再生能力强,循环使用寿命长,是一种很有价值的高效脱硼吸附剂。 相似文献
110.
分光光度法测定用于废氧化铝载体铂催化剂中铂含量。铂被还原成铂黑从杂质中分离出,用王水溶解形成六氯铂酸盐酸溶液,加入氯化亚锡形成橙黄色络合物溶液在403nm进行测定。对该方法的回收率,钼存在对测定的影响进行了研究,方法回收率98~102%,在10-6数量级,即使钼浓度与铂浓度相等并不影响铂的测定 相似文献