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121.
122.
从1株海绵内生真菌(Alternaria sp.)链格孢菌的发酵液中提取胞外多糖,对其进行Q Sepharose FF离子交换色谱分离纯化,得到2个组分JJY-W和JJY-S。运用各种化学方法及波谱方法对JJY-W和JJY-S的理化性质及结构进行分析,并对多糖清除自由基活性进行了评价。结果表明,JJY-W和JJY-S的分子量分别为1.4KD和1.8KD;JJY-W以半乳糖、葡萄糖为主,含有少量甘露糖,摩尔比为:甘露糖∶葡萄糖∶半乳糖=1∶2.5∶11。JJY-S以甘露糖、葡萄糖为主,含有少量半乳糖,摩尔比为:甘露糖∶葡萄糖∶半乳糖=3∶2∶1。JJY-W总糖含量为46.3%,未检测出糖醛酸,蛋白含量为2%。JJY-S总糖含量为52%,糖醛酸含量为6.1%,蛋白含量为14%。活性分析表明,2种多糖均具有一定的体外抗氧化活性,并随着浓度的增加清除自由基能力均增强,JJY-W清除DPPH自由基的活性要强于JJY-S,而JJY-S清除OH.自由基的活性要强于JJY-W。 相似文献
123.
晋西北地区表层土壤粒度与地球化学元素组成 总被引:1,自引:1,他引:0
对晋西北地区表层土壤的物质组成进行研究,可以明确其物质来源、沉积环境及化学风化特征。选择区内表层土壤(深度0、10、20 cm)及其附近的河流沉积物,进行粒度和化学元素组成测试。结果表明:(1)晋西北地区表层土壤粒度组成以黏土和粉沙为主,且有自地表向下粗颗粒组分含量增加的趋势。(2)常量化学元素组成以SiO2、Al2O3、CaO、Fe2O3为主,其余元素含量均较低。化学元素组成模式表明研究区内表层土壤物质与黄土高原腹地黄土有相同的物质源区,黄河河流沉积物对其贡献不大。(3)晋西北表层土壤的CIA值为52.70~57.89,平均54.06,说明它们的化学风化程度较低,处于早期的脱Na、Ca阶段。这是由于研究区地理位置比洛川更靠北,气温和降水量均低于洛川,降水量与兰州相差不大,但是年平均气温和年温差比兰州低。该研究明确了晋西北地区表层土壤的物质组成特征,为区域潜在沙漠化危害防治提供了数据支撑。 相似文献
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125.
It is a conventional method for petroleum prospecting to generally use paraffin hydrocarbon as basic indexes of oil and gas. This conventional geochemical technology, however, shows some limits in the prospecting as paraffin is vulnerable to influences from human and biologic activities. Consequently, BTEX (short for benzene, toluene, ethyl benzene and xylem, which are direct biomarkers) among aromatic hydrocarbon series has been taken into account for the oil and gas prediction. Domestic and foreign study results demonstrate that BTEX is hardly disturbed and can well indicate oil and gas reservoirs. Based on measured data from a South China Sea area, the present authors have used self-developed visual assessment software for petroleum prospecting has been used to process data, strip background anomalies, and outline significant BTEX anomalies. By comparison with stratigraphic profiles of the target area, it is confirmed that BTEX is a good indication of marine oil and gas during the petroleum prospecting. 相似文献
126.
瘤状软骨凹顶藻化学成分研究 总被引:1,自引:0,他引:1
采用硅胶柱色谱以及Sephadex LH-20凝胶色谱手段,对海洋红藻瘤状软骨凹顶藻(Chondrophycus papillous Garbary et Harper)进行化学成分研究,分离得到5个化合物.通过MS、NMR等方法对得到的化合物进行结构确证,分别鉴定为邻苯二甲酸二丁酯(Ⅰ),邻苯二甲酸二异辛酯(Ⅱ),胆甾醇(Ⅲ),植醇(Ⅳ)和4-羟基苯甲醛(Ⅴ).所有化合物均为首次从该种海藻中分离得到.通过MTT法对得到的单体化合物进行细胞毒活性筛选,结果显示所有化合物在10 mg/L浓度下均无明显活性. 相似文献
127.
海洋红藻多管藻内生真菌EN-22 的化学成分研究 总被引:4,自引:0,他引:4
对采自广西涠州岛近海多管藻(Poiysiphonia urceolata)分离到的一株内生真菌EN-22的次生代谢产物的化学成分进行了研究.利用正相硅胶柱层析、葡聚糖凝胶Sephadex LH-20柱层析、制备薄层层析(PTLC)以及重结晶等分离手段从该菌发酵液中分离得到15个化合物,通过一维、二维核磁共振技术、质谱技术等鉴定了所有化合物的结构,分别为:4-(4-喹啉)-4-羟基-2-丁酮(1),3-羟基-3-(2-氧丙基)吲哚-2-酮(2),3-吲哚乙醇(3),3-吲哚甲酸(4),2-羟基-3-吲哚丙酸(5),2-酮-3-吲哚乙醇(6),3,3-二吲哚-2-羟基-丙醇(7),β-咔啉(8),尿嘧啶(9),环-(S-脯氨酸-S-异亮氨酸)(10),(22E,24R)-3β,5α,9α-三羟基麦角甾-7,22-二烯-6-酮(11),(22E,24R)-5α,6α-环氧麦角甾-8,22-二烯-3β,7α-二醇(12),5α,6α-环氧-24(R)-甲基胆甾-7,22-二烯-3β-醇(13),胡萝卜苷(14),过氧化麦角甾醇(15);其中化合物1和2为新天然产物,并首次报道化合物1的碳谱数据. 相似文献
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129.
Twenty-four compounds including eight steroids (1-8), nine triterpenoids (9-16, 24), three flavonoids (20-22), and four benzenecarboxylic derivatives (17-19, 23) were isolated and identified from stems and twigs of medicinal mangrove plant Sonneratia caseolaris. The structures of the isolated compounds were determined by extensive analysis of their spectroscopic data. Among these metabolites, compounds 1, 4-20 and 22-24 were isolated and identified for the f'urst time from S. caseolaris. In the in vitro cytotoxic assay against SMMC-7721 human hepatoma cells, compound 21 (3',4',5,7-tetrahydroxyflavone)exhibited significant activity with IC50 2.8 μg/mL, while oleanolic acid (14), 3,3'-di-O-methyl ether ellagic acid (18), and 3,3',4-O-tri-O-methyl ether ellagic acid (19) showed weak activity. None of these compounds displayed significant antibacterial activites. 相似文献
130.
The source rock from which the sillimanite gneisses derive mainly was the biotite plagioclase gneiss in the Larsemann Hills. It is the deformation-metamorphism process under special pressure and temperature condition, not the original rock compositions, that controls the presence of sillimanite. To a great degree, the sillimanite gneiss was the mixture of the detaining materials of the migrating felsic melt from the bt-plagioclase gneiss that underwent partial melting and the relics when the melt was removed. In sillimanitization the original rock had been changed substantially in chemical composition. The related metamorphism process severely deviated from the isochemical series, the process was of, therefore, an open system. In addition, the Al2O3 contents of the original rock was an important, but not critical factor for the formation of sillimanite, i.e., the sillimanite-bearing rock need not be of aluminum rich in composition, and vise contrarily, the aluminum rock may not produce sillimanite. The authors of the present paper postulate that the source rock from which the aluminum rich rock derives need not be of aluminum rich, but sillimanitization is generally the Al2O3 increasing process. The aluminum rich sediments such as clay or shale need not correspond directly to sillimanite-rich gneisses. No argillaceous rock present equals to sillimanite-rich gneiss in chemical composition. The protoliths to the sillimanite gneisses from the Larsemann Hills, east Antarctica, and their adjacent area may be pelite, shale greywacke, sub-greywacke, quartz sandstone and quartz-tourmalinite. If correct, the conclusion will be of significant implication for the determination of the sillimanite gneiss formation process and the reconstruction of the protolith setting. 相似文献