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921.
Blood clotting exhibits various important functions, including the prevention of body fluid loss and invasion of pathogens in shrimp. The effects of pathogenic Vibrio harveyi on plasma of white shrimp (Litopenaeus vannamei) in vitro and in vivo were investigated in this study. The clotting protein (coagulogen) in plasma of white shrimp pre‐incubated with extracellular products (ECP) of V. harveyi was found apparently decreased and fast‐migrated in crossed immunoelectrophoresis (CIE) gels. In addition, the coagulogen had been degraded to many low molecular‐weight protein bands in plasma pre‐incubated with ECP on sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS‐PAGE) gels. When pre‐challenged with bacterial cells and ECP of V. harveyi, the white shrimp began to die at about 30 and 16 h respectively. Moreover, plasma coagulogen was decreased more obvious in shrimp challenged with ECP than that with bacterial cells as visualized in CIE gels, and total plasma protein in both group of shrimp were all decreased. Haemolymph withdrawn from moribund shrimp pre‐challenged with V. harveyi or its ECP was observed unclottable. However, the addition of clotting factors (transglutaminase and/or Ca2+) to these unclottable plasma could apparently promote their re‐clotting ability as jelly‐like solid observed in microtubes. The recovery of clotting ability of plasma from moribund shrimp was due to the reformation of coagulogen (200 kDa) after adding the two clotting factors as shown on CIE and SDS‐PAGE gels. The present results suggest that the infection of V. harveyi in white shrimp may not only degrade coagulogen but also influence the presence of transglutaminase and Ca2+ ion.  相似文献   
922.

The ability to determine the presence and identity of sugars in the guts of adult parasitoids in the field would aid researchers in addressing long-standing problems in parasitoid ecology. Until very recently, however, gut sugar analyses have not been carried out on parasitoids. This is despite the development and use of methodologies for gut sugar analyses in biting flies (mosquitoes, sand-flies, black-flies, horse- and deer-flies, and biting midges) for decades. Methods used have been the cold anthrone test for the detection of gut sugars, and various forms of chromatography for the identification of gut sugars. We review the use of these methods in biting fly research and then describe the nascent field of gut sugar analyses in parasitoids. Both cold anthrone and chromatography tests have begun to be used on field-caught parasitoids, and we describe progress from our own work. We used cold anthrone on the aphid parasitoid Aphelinus albipodus (Hymenoptera: Aphelinidae), and results from one field study show that approximately one-fifth of individuals tested were positive for gut sugars. The characteristics of the field site point to the primary source of these gut sugars as being aphid honeydew. We also analysed the gut contents of Diadegma insulare (Hymenoptera: Ichneumonidae), a parasitoid of diamondback moth. In this case, HPLC analyses showed that over 85% of field-captured individuals had fed upon sugars. These same analyses suggested that honeydew may have been a major source of the gut sugars in this case also, but the sugar profiles suggest some nectar feeding. Understanding the importance of various sugar sources on parasitoid activity and effectiveness will facilitate the incorporation of sugar sources in habitat manipulation programmes as a part of IPM.  相似文献   
923.
Abstract

Trials were carried out in Upper Volta to assess equipment for the application of insecticides as aerosol from helicopters for the control of riverine tsetse flies (G. tachinoides). Flying techniques were developed to direct aerosols in the downwash of the helicopter to tsetse breeding sites close to the water's edge. Good penetration of droplets below the riverine canopy was achieved during the late afternoon and early morning when weather conditions were very stable.  相似文献   
924.
Random amplified polymorphism DNA (RAPD) and bulk segregant analysis (BSA) approaches were used to characterize the molecular marker linked to the Phytophthora infestans resistance gene Ph-3 in tomato. A total of 800 RAPD primers were screened. One RAPD marker UBC#602 was identified to be tightly linked to the Ph-3 gene. The marker was successfully converted into a co-dominant sequence characterized amplified region (SCAR) marker. The SCAR marker SCU602 was used to analyze 96 F2 progenies and fitted the expected 1:2:1 Mendelian segregation ratio. Forty one tomato inbred lines were screened using the SCAR marker in comparison with a reference marker linked to the Ph-3 gene and both markers gave the same results. SCU602 was further validated for association to resistance and its potential in MAS in 72 tomato lines and cultivars. The marker identified three genotypes harbouring the resistance allele. This SCAR marker can be used in breeding programs for the selection of the Ph-3 gene for Phytophthora infestans resistance.  相似文献   
925.
Abstract

Experiments have been carried out in the Ivory Coast to assess the performance of a prototype rapid release system to apply larvicides for the control of S. damnosum, the vector of onchocerciasis. The equipment was fitted to a Pilatus Porter aircraft and was used to apply Abate larvicide to a large river during conditions of low water level. It was shown that the equipment could accurately deliver volumes of larvicide between one and 50 l and that these quantities could be placed exactly along chosen points in the river, provided the aircraft was flown along the direction of the watercourse. Satisfactory control of S. damnosum larvae was achieved at three sites using a dosage rate of 0.05 ppm/10 min of waterflow. However, it was recommended that a dosage of 0.1 ppm/10 min be adopted in future work because some of the more extensive sites treated were underdosed. It was not possible to assess the biological effectiveness of the equipment for treating small rivers, but physical tests were carried out which suggest that the system should be suitable for applying larvicide to rivers as narrow as five metres width. Recommendations were made to improve the reliability of the equipment for use in an operational onchocerciasis programme.  相似文献   
926.
927.
The population of Phytophthora infestans on potato landraces in three provinces (Carchi, Chimborazo and Loja) of Ecuador was analysed. All isolates (= 66) were of the A1 mating type. Simple sequence repeats (SSR) were used to assess the genetic diversity of the isolates. The P. infestans isolates from the potato landraces grouped in a single clade together with reference isolates belonging to the clonal lineage EC‐1. In the 66 SSR profiles obtained, 31 multilocus genotypes were identified. The 66 isolates constituted 49 different races according to the Solanum demissum differential set ( R1 to R11). The P. infestans population was complex and virulent on 4 to 11 R genes. Analysis showed that the subclonal variation in the Ecuadorian EC‐1 clone is increasing over time and is much larger than clonal variation in lineages in the Netherlands and Nicaragua, suggesting high mutation rates and little or no selection in Ecuador.  相似文献   
928.
In this study fusaricidin, a cyclic depsipeptide isolated from Paenibacillus polymyxa E681 (E681), was demonstrated to control Phytophthora blight infection caused by Phytophthora capsici in red-pepper. The minimal inhibitory concentration (MIC) of fusaricidin was found to be 16 ppm against P. capsici. The disease severity of P. capsici was 40% at 0.1 ppm of fusaricidin when compared with water-treated control (81.7%) on post-treatment, whereas the disease severities on pre-treatment were 45% and 83.3% in fusaricidin (0.1 ppm) and water-treated control, respectively, in red-pepper plants. Significant (P?<?0.05) disease suppression was observed on treatment with fusaricidin (0.1 ppm) by foliar spray and soil drench. The disease severity was drastically reduced to 3.3% by soil drench of fusaricidin (1.0 ppm), whereas in water-treated control, the disease severity was 83.3% in the first experiment. Fusaricidin at 0.1 ppm reduced disease severity of P. capsici to 27.5% when compared with positive control (43.1%) and water-treated control (66.2%) in the second experiment. Soft rot disease in tobacco was suppressed upon treatment with fusaricidin at 1.0 ppm by leaf infiltration. RT-PCR analyses of Arabidopsis thaliana revealed that there was an up-regulation of pathogenesis-related (PR) gene expression in wild type A. thaliana (Col-0), while there was no accumulation of PR genes, which implies that the mechanism of protection might be based on a salicylic acid-dependent pathway. This is the first report that fusaricidin exhibits protection against plant pathogens in addition to activity as an antibiotic agent. Hence, E681 can play a role in plant protection by secretion of ISR elicitors including fusaricidin.  相似文献   
929.
A nationwide investigation was performed to detect the presence of 1014 mutation(s) in voltage gated sodium channel (kdr) gene of Culex quinquefasciatus from 14 residential areas across 13 states and a federal territory in Malaysia. Molecular genotyping of kdr mutation was performed via a modified three tubes allele-specific-polymerase chain reaction (AS-PCR) and direct sequencing of kdr gene. Based on the results of AS-PCR, homozygous susceptible (SS) genotype was found in nine out of 14 populations with 38 individuals from a total sample size of 140. Heterozygous (RS) genotype was most predominant (99 individuals) and distributed across all study sites. Homozygous resistance (RR) genotype was detected in Perak (one individual) and Selangor (two individuals). The resistance kdr allele frequencies ranged from 0.1 to 0.55, with the highest being detected in Cx. quinquefasciatus population from Selangor. This study has documented the first field-evolved instance of 1014F mutation in Malaysian mosquitoes and the findings of this study could be utilized in the implementation of strategic measures in vector control programs in Malaysia.  相似文献   
930.
Forest compositional shifts in response to climate change are likely to be initially detectable in the understory tree regeneration layer near species range limits. Because many factors in addition to climate, such as seedbed and soil characteristics, overstory composition, and interactions with other understory biota, drive tree regeneration trends, a thorough understanding of the relative importance of all variables as well as their interrelationships is needed. The range limits of several widespread temperate and boreal tree species overlap in the upper Great Lakes region, USA, thus facilitating an observational study over relatively short regional climate gradients. We used redundancy analysis and variation partitioning to quantify the unique, shared, and total explanatory power of four sets of explanatory variables. The results showed that all four variable sets (climate 9.5 %, understory environment 13.7 %, overstory composition 26.3 %, and understory biota 13.8 %) were significantly associated with tree regeneration compositional variation in mixed temperate–boreal forests. Partitioning also revealed high confounded or shared explanatory power, but also that each set contributed significant unique explanatory power not shared with other sets. Spatial patterning in regeneration composition was strongly related to broad scale environmental patterns, while the large majority of unexplained variation did not have a detectable spatial structure, suggesting factors with local scale variability. Future forest shifts across the landscape will depend not only on the rate and direction of climate change but also on how the strengths and interrelationships among other explanatory variables, such as overstory composition and understory biota, shift with a changing climate.  相似文献   
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