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81.
Ronald P. Neilson 《Plant Ecology》1987,70(3):135-147
New methods of weather analysis accompanied by microhabitat ‘bioassays’ have been applied in several case studies to demonstrate effects of atmospheric processes on patterns of community composition and structure and potential species evolution. Average spatial and seasonal airmass dynamics which determine regional and elevational patterns of relative microhabitat favorability, were found to vary between a recent global warming trend (ca 1900 to 1940) and the subsequent global cooling trend (ca 1940 to 1970). These apparently systematic spatial and temporal shifts in weather were related to plant establishment patterns and community composition and structure. The proposed causal mechanisms function, in part, through regional shifts in microhabitat size. These effects are similar to larger scale, longer term shifts deduced from the late Quaternary fossil record. By modifying the spatial approach, month-to-month and year-to-year variability of weather has been examined for the last 130 years at individual points in southwestern North America. Three climatic regimes (the end of the Little Ice Age, the recent warming trend and the recent cooling trend) exhibited distinct year-to-year patterns of weather that can be related to the establishment of different kinds of plants (e.g., C4 grasses versus C3 shrubs). Oscillations between different temporal climatic regimes appear to promote the episodic establishment of different life forms, but not necessarily their local extinction. The two methods of weather analysis have been combined in a regional assessment of climatic controls of different biomes in space and time with a primary focus on the Chihuahuan desert. Natural ecotones between the Chihuahuan desert and neighboring biomes are clearly related to large scale airmass dynamics associated with seasonal oscillations in jetstream position. The weather patterns controlling ecotonal positions result from seasonal topographic influences on the general circulation of the atmosphere. The apparent stability of these patterns allows causal hypotheses of biogeographic dynamics and the evolution of physiological traits and life history characteristics. 相似文献
82.
The reactions of singlet oxygen (1O2) with cis and trans butenes-1,1,1-d3, at—80°C in Freon-11, show a product isotope effect (kH/kD) of 1.38 and 1.25 respectively. Isomerization of the starting materials or formation of dioxetanes were not observed during the course of the photooxygenation. Together with the isotope effects on the reactions of tetramethylethylene-d6 isomers with singlet oxygen, these results require the reversible formation of a perepoxide or charge transfer intermediate. 相似文献
83.
84.
经调查,蚕豆田的昆虫和蜘蛛,计有68种,其中属农作物害虫的有18种,天敌有50种。本文还对蚕豆田节肢类的优势种群、种群动态及其群落特征进行了分析,阐明了保护蚕豆田中的天敌对控制后茬作物害虫的重要意义。 相似文献
85.
High light treatments were given to attached leaves of pumpkin (Cucurbita pepo L.) at room temperature and at 1°C where the diffusion- and enzyme-dependent repair processes of Photosystem II are at a minimum. After treatments, electron transfer activities and fluorescence induction were measured from thylakoids isolated from the treated leaves. When the photoinhibition treatment was given at 1°C, the Photosystem II electron transfer assays that were designed to require electron transfer to the plastoquinone pool showed greater inhibition than electron transfer from H2O to paraphenyl-benzoquinone, which measures all PS II centers. When the light treatment was given at room temperature, electron transfer from H2O to paraphenyl-benzoquinone was inhibited more than whole-chain electron transfer. Variable fluorescence measured in the presence of ferricyanide decreased only during room-temperature treatments. These results suggest that reaction centers of one pool of Photosystem II, non-QB-PS II, replace photoinhibited reaction centers at room temperature, while no replacement occurs at 1°C. A simulation of photoinhibition at 1°C supports this conclusion.Abbreviations BSA
bovine serum albumin
- Chl
chlorophyll
- DCMU
3-(3,4,-dichlorophenyl)-1,1,-dimethylurea
- DCPIP
dichlorophenol-indophenol (2,6-dichloro-4((4-hydroxyphenyl)imino)-2,5-cyclohexadien-1-one)
- DPC
diphenyl carbazide (2,2-diphenylcarbonic dihydrazide)
- FeCN
ferricyanide (hexacyanoferrate(III))
- app
apparent quantum yield of photosynthetic oxygen evolution
- MV
methyl viologen (1,1-dimethyl-4,4-bipyridinium dichloride)
- PPBQ
phenyl-p-benzoquinone
- PPFD
photosynthetic photon flux density
- PQ
pool plastoquinone
- QB
secondary quinone acceptor of PS II
- RT
room temperature
- WC
whole chain electron transfer 相似文献
86.
植物群落演替与土壤发展之间的关系 总被引:46,自引:0,他引:46
张全发;郑重;金义兴 《武汉植物学研究》1990,8(4):325-334
本文运用植物群落中植物优势种的重要值与相对应子群落的土壤特征值直接相关联的分析方法,对湖北宜昌大老岭的桦(Betula)、栎(Quercus)、栗(Castanea)七个群落类型的三个演替途径的土壤动态进行分析,结果表明:在植物群落的演替过程中,土壤中的Ca、pH值减少;离子代换量增加;Na、Mg、NH_4+-N、速效P、速效K、有机质的含量是随着物种的变化而呈不同的趋势。因此,植物群落的演替是生态系统的动态过程。 相似文献
87.
88.
Luísa M. D. R. S. Martins Armando J. L. Pombeiro Richard A. Henderson 《Inorganica chimica acta》1996,250(1-2):311-315
The kinetics of the displacement reactions of the bromide ligands of trans-[FeBr2(depe)2] (depe = Et2PCH2CH2PEt2) by the organonitrile NCCH2C6H4OMe-4, in tetrahydrofuran (either in the absence or in the presence of added Br−), to give the corresponding mono- and dinitrile complexes trans-[FeBr(NCCH2C6H4OMe-4)(depe)2]+ and trans-[Fe(NCCH2C6H4OMe-4)2(depe)2]2+, have been investigated by stopped-flow spectrophotometry. The substitution reaction occurs by a mechanism involving rate-limiting dissociation of bromo ligands to form the unsaturated intermediates [FeBr(depe)2]+ (k1 = 1.52 ± 0.02 s−1) and [Fe(NCR)(depe)2]2+ (k3 = 0.063 ± 0.008 s−1) which add the nitrile ligand to form those nitrile complexes. The competition between the nitrile and Br− for such metal centres has also been investigated and a stronger inhibiting effect of added Br− is observed for the substitution of the second bromo ligand relative to the first one. The kinetic data are rationalized in terms of π-electronic effects of these unsaturated metal centres and of the bromide and nitrile ligands. 相似文献
89.
90.