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941.
Determinants of woody cover in African savannas 总被引:8,自引:0,他引:8
Sankaran M Hanan NP Scholes RJ Ratnam J Augustine DJ Cade BS Gignoux J Higgins SI Le Roux X Ludwig F Ardo J Banyikwa F Bronn A Bucini G Caylor KK Coughenour MB Diouf A Ekaya W Feral CJ February EC Frost PG Hiernaux P Hrabar H Metzger KL Prins HH Ringrose S Sea W Tews J Worden J Zambatis N 《Nature》2005,438(7069):846-849
Savannas are globally important ecosystems of great significance to human economies. In these biomes, which are characterized by the co-dominance of trees and grasses, woody cover is a chief determinant of ecosystem properties. The availability of resources (water, nutrients) and disturbance regimes (fire, herbivory) are thought to be important in regulating woody cover, but perceptions differ on which of these are the primary drivers of savanna structure. Here we show, using data from 854 sites across Africa, that maximum woody cover in savannas receiving a mean annual precipitation (MAP) of less than approximately 650 mm is constrained by, and increases linearly with, MAP. These arid and semi-arid savannas may be considered 'stable' systems in which water constrains woody cover and permits grasses to coexist, while fire, herbivory and soil properties interact to reduce woody cover below the MAP-controlled upper bound. Above a MAP of approximately 650 mm, savannas are 'unstable' systems in which MAP is sufficient for woody canopy closure, and disturbances (fire, herbivory) are required for the coexistence of trees and grass. These results provide insights into the nature of African savannas and suggest that future changes in precipitation may considerably affect their distribution and dynamics. 相似文献
942.
Parasites and climate synchronize red grouse populations 总被引:2,自引:0,他引:2
There is circumstantial evidence that correlated climatic conditions can drive animal populations into synchronous fluctuations in abundance. However, it is unclear whether climate directly affects the survival and fecundity of individuals, or indirectly, by influencing food and natural enemies. Here we propose that climate affects trophic interactions and could be an important mechanism for synchronizing spatially distributed populations. We show that in specific years the size of red grouse populations in northern England either increases or decreases in synchrony. In these years, widespread and correlated climatic conditions during May and July affect populations regionally and influence the density-dependent transmission of the gastrointestinal nematode Trichostrongylus tenuis, a parasite that reduces grouse fecundity. This in turn forces grouse populations into synchrony. We conclude that specific climatic events may lead to outbreaks of infectious diseases or pests that may cause dramatic, synchronized changes in the abundance of their hosts. 相似文献
943.
944.
Wildermuth S Hofferberth S Lesanovsky I Haller E Andersson LM Groth S Bar-Joseph I Krüger P Schmiedmayer J 《Nature》2005,435(7041):440
Today's magnetic-field sensors are not capable of making measurements with both high spatial resolution and good field sensitivity. For example, magnetic force microscopy allows the investigation of magnetic structures with a spatial resolution in the nanometre range, but with low sensitivity, whereas SQUIDs and atomic magnetometers enable extremely sensitive magnetic-field measurements to be made, but at low resolution. Here we use one-dimensional Bose-Einstein condensates in a microscopic field-imaging technique that combines high spatial resolution (within 3 micrometres) with high field sensitivity (300 picotesla). 相似文献
945.
Seismological evidence for mosaic structure of the surface of the Earth's inner core 总被引:2,自引:0,他引:2
The transition from the Earth's solid inner core to liquid outer core is the location where the inner core grows and from which compositional convection in the outer core originates. Most seismological models of the Earth describe the inner-core boundary as sharp and simple, although experimental data requiring the presence of a thin transition layer at the bottom of the outer core have been reported. The density jump at the inner-core boundary--an important parameter determining gravitational energy release and constraining the compositional difference between the inner and outer core-is also not well known. Estimates of this density jump obtained using free-oscillation eigenfrequencies give low values of 0.25-1.0 g cm(-3), whereas a method using the amplitude ratio of core-reflected phases yielded values of 0.6-1.8 g cm(-3) (refs 14, 15, 16-17). Here we analyse properties of waves precritically reflected from the Earth's inner core (PKiKP phases) that show significant variability in amplitude, consistent high-frequency content and stable travel times with respect to a standard Earth model. We infer that the data are best explained by a mosaic structure of the inner core's surface. Such a mosaic may be composed of patches in which the transition from solid inner to liquid outer core includes a thin partially liquid layer interspersed with patches containing a sharp transition. 相似文献
946.
947.
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia 总被引:21,自引:0,他引:21
Skibinski G Parkinson NJ Brown JM Chakrabarti L Lloyd SL Hummerich H Nielsen JE Hodges JR Spillantini MG Thusgaard T Brandner S Brun A Rossor MN Gade A Johannsen P Sørensen SA Gydesen S Fisher EM Collinge J 《Nature genetics》2005,37(8):806-808
We have previously reported a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to chromosome 3 (FTD3). Here we identify a mutation in CHMP2B, encoding a component of the endosomal ESCRTIII complex, and show that it results in aberrant mRNA splicing in tissue samples from affected members of this family. We also describe an additional missense mutation in an unrelated individual with FTD. Aberration in the endosomal ESCRTIII complex may result in FTD and neurodegenerative disease. 相似文献
948.
Mutations in SEPT9 cause hereditary neuralgic amyotrophy 总被引:7,自引:0,他引:7
Kuhlenbäumer G Hannibal MC Nelis E Schirmacher A Verpoorten N Meuleman J Watts GD De Vriendt E Young P Stögbauer F Halfter H Irobi J Goossens D Del-Favero J Betz BG Hor H Kurlemann G Bird TD Airaksinen E Mononen T Serradell AP Prats JM Van Broeckhoven C De Jonghe P Timmerman V Ringelstein EB Chance PF 《Nature genetics》2005,37(10):1044-1046
Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant recurrent neuropathy affecting the brachial plexus. HNA is triggered by environmental factors such as infection or parturition. We report three mutations in the gene septin 9 (SEPT9) in six families with HNA linked to chromosome 17q25. HNA is the first monogenetic disease caused by mutations in a gene of the septin family. Septins are implicated in formation of the cytoskeleton, cell division and tumorigenesis. 相似文献
949.
Extent, duration and speed of the 2004 Sumatra-Andaman earthquake imaged by the Hi-Net array 总被引:1,自引:0,他引:1
The disastrous Sumatra-Andaman earthquake of 26 December 2004 was one of the largest ever recorded. The damage potential of such earthquakes depends on the extent and magnitude of fault slip. The first reliable moment magnitude estimate of 9.0 was obtained several hours after the Sumatra-Andaman earthquake, but more recent, longer-period, normal-mode analyses have indicated that it had a moment magnitude of 9.3, about 2.5 times larger. Here we introduce a method for directly imaging earthquake rupture that uses the first-arriving compressional wave and is potentially able to produce detailed images within 30 min of rupture initiation. We used the Hi-Net seismic array in Japan as an antenna to map the progression of slip by monitoring the direction of high-frequency radiation. We find that the rupture spread over the entire 1,300-km-long aftershock zone by propagating northward at roughly 2.8 km s(-1) for approximately 8 minutes. Comparisons with the aftershock areas of other great earthquakes indicate that the Sumatra-Andaman earthquake did indeed have a moment magnitude of approximately 9.3. Its rupture, in both duration and extent, is the longest ever recorded. 相似文献
950.
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease 总被引:5,自引:0,他引:5
Züchner S Noureddine M Kennerson M Verhoeven K Claeys K De Jonghe P Merory J Oliveira SA Speer MC Stenger JE Walizada G Zhu D Pericak-Vance MA Nicholson G Timmerman V Vance JM 《Nature genetics》2005,37(3):289-294
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous group of peripheral neuropathies. Different chromosomal loci have been linked with three autosomal dominant, 'intermediate' types of CMT: DI-CMTA, DI-CMTB and DI-CMTC. We refined the locus associated with DI-CMTB on chromosome 19p12-13.2 to 4.2 Mb in three unrelated families with CMT originating from Australia, Belgium and North America. After screening candidate genes, we identified unique mutations in dynamin 2 (DNM2) in all families. DNM2 belongs to the family of large GTPases and is part of the cellular fusion-fission apparatus. In transiently transfected cell lines, mutations of DNM2 substantially diminish binding of DNM2 to membranes by altering the conformation of the beta3/beta4 loop of the pleckstrin homology domain. Additionally, in the Australian and Belgian pedigrees, which carry two different mutations affecting the same amino acid, Lys558, CMT cosegregated with neutropenia, which has not previously been associated with CMT neuropathies. 相似文献