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101.
The eukaryotic cell membrane is thought to consist of a mobile bilayer of phospholipid, sometimes intercalated with sterols, in which peripheral and transmembrane proteins are embedded. This provides a model whereby the mode of action of many fungicidal and herbicidal compounds can be rationalised and understood. Some compounds, such as the polyene antibiotics, steroidal saponins and certain phytoalexins, induce membrane malfunction by direct insertion, often complexing with vital components. Others, such as paraquat and the nitrodiphenyl ether herbicides, cause membrane damage by inducing lipid peroxidations. Furthermore, there are many compounds, including the sterol-biosynthesis-inhibiting fungicides and the aryloxyphenoxypropionate and cyclohexanedione herbicides, which interfere with the biosynthesis of membrane components. Because membrane structure is fundamentally similar in eukaryotes, it is important to discover the reasons for any differential toxicity displayed by these compounds and, if necessary, to find ways of optimising desirable patterns of selectivity.  相似文献   
102.
The effect of acifluorfen and oxyfluorfen on chlorophyll bleaching, lipid peroxidation and photosynthesis in pea leaf discs was studied. Both her- bicides induced light-dependent bleaching and lipid peroxidation, the level of damage being greater at higher light intensities. Photosynthetic carbon dioxide fixation was only partially inhibited in treated leaf discs incubated in darkness, thus indicating that these herbicides did not inhibit photo- synthesis as a primary mode of action. Leaf discs maintained in darkness showed no visible signs of injury, and light-dependent herbicide-induced damage was reduced by incubating discs under nitrogen, orpre-incubating them with the electron-transport inhibitor monuron. It is suggested that acifluorfen and oxyfluorfen are activated by a light-dependent process, which requires photosynthetic electron transport.  相似文献   
103.
The effects of permethrin on native and caged fish when aerially applied directly to forest streams at dosages between 8.8 and 70 g ha?1 were studied between 1976 and 1981. None of the applications caused mortality of caged or native fish in streams. Trout and salmon diets were altered by the treatments due to effects on fish food organisms. The duration of the effects varied from several months to over a year with increasing dosage. Reductions in salmonid growth rates and reductions in fish densities in treated areas, presumably due to emigration, were documented following severe impacts on aquatic invertebrates in salmon nursery streams. Growth rates and population densities both recovered within four months after treatment.  相似文献   
104.
A series of experiments was conducted between 1977 and 1981 to evaluate the effects of aerially applied permethrin on forest stream invertebrates. All permethrin applications to forest streams resulted in large drift increases, and most produced measurable reductions in benthos density. Recovery of benthic fauna following the various permethrin applications was apparent from 1 to 18 months post-spray. In double-application experiments, the second treatments reduced benthos density to a point at which recovery of numbers was slower than after the impact resulting from a single application of the same dosage.  相似文献   
105.
Two analogues of the aphid alarm pheromone (E)-β-farnesene, a trifluorofarnesene and a difluoro-1-norfarnesene, were found to be highly active and were more readily detectable than the parent compound. For (Z)-hexadec-11-enal, a component of some lepidopteran sex attractant pheromones, replacement of the carbonyl oxygen with a difluoromethyl group to give a difluoroheptadecadiene resulted in loss of activity. A trifluoroacetoxyhexadecanolide was a more volatile analogue of the mosquito oviposition pheromone (?)-(5R,6S)-6-acetoxy-5-hexadecanolide and was highly active.  相似文献   
106.
The vapour pressures of the separate isomers of permethrin have been determined over a range of temperatures by two laboratories using different versions of the gas saturation method. A statistical analysis of the sets of data from the two laboratories shows no significant differences for the cis isomers but a small difference in the 20°C extrapolated values for the trans isomer exists. However, this difference is discounted as arising from experimental error and the mean values of the estimated vapour pressures at 20°C are given as 2.5 μPa (cis) and 1.5 μPa (trans).  相似文献   
107.
Over 100 benzyl esters of pyrethroidal acids were synthesised and tested for insecticidal activity to establish detailed structure–activity relationships in compounds with side-chains similar to those in the natural pyrethrins. Alkenyl, and corresponding alkynyl, side-chains were effective, both at the 3- and 4-positions, as were side-chains with extended substitution in either E or Z forms. A cyano group at the α-position increases activity if the side-chain is at C-3, but lowers it drastically if the substituent is at C-4. Similarly, methyl groups at C-2 and/or C-6 may increase activity whether the unsaturated side-chain is at C-3 or C-4, but only in the absence of an α-cyano group.  相似文献   
108.
Two experimental insecticides, AC 303,630 and MK 244, were tested against a laboratory colony and three field strains of Pseudoplusia includens (Walker). Topical application bioassays indicated that permethrin resistance in the field strains ranged from 3.9 to 489.0-fold. In leaf dip bioassays, LC50 and LC90 values for AC 303,630 ranged from 6.7 to 15.1 mg litre ?1 and 8.7 to 28.2 mg litre ?1, respectively, for third-instar larvae. The Louisiana 1991 field strain was significantly more susceptible to AC 303,630 than the laboratory and other field strains. The LC50 (but not LC90) for the Louisiana 1992 field strain was significantly higher than that of the laboratory strain. However, there was no difference in toxicity of AC 303,630 between the field strain with the highest level of permethrin resistance and the laboratory strain. LC50 and LC90 values for MK 244 in leaf dip bioassays ranged from 0.014 to 0.023 mg litre ?1 and 0.079 to 0.174 mg litre ?1, respectively. There were no significant differences in LC 50 or LC 90 among any of the strains for MK 244. Field trials in soybean were also conducted in 1991 and 1992 in an area of Louisiana where permethrin efficacy against P. includens has declined. In both years, AC 303,630 at 0.11–0.22 kg ha ?1, and MK 244 at 0.0042–0.0084 kg ha ?1, provided significantly better control than permethrin at 0.11 kg ha ?1, and control equal to the recommended standard, thiodicarb. These studies indicate no cross-resistance exists between the experimental insecticides and permethrin.  相似文献   
109.
The effects of application rate, volume, solvent and soil moisture content on the kinetics of mineralization and degradation, of [14C] permethrin have been studied in a sandy loam soil under standard laboratory conditions. During the incubation period, up to 32 days, the temperature and moisture level of the soil were controlled. Apart from the effects of application rate, which have been widely reported, application volume had the most significant effect on mineralization rate and T1/2. [14C]Permethrin, at a level of a 1 mg kg?1 in the soil, applied in 100 μl of methanol, resulted in the evolution of 14% of the applied radiochemical as [14C] carbon dioxide over 30 days. The same level applied in 1000 μl mineralized at a faster rate, with 30% [14C]carbon dioxide evolved over 30 days. The test chemical applied to soil in methanol mineralized at a significantly faster rate than a similar concentration applied in ethanol. There was no significant difference when comparing applications made using acetonitrile with those using methanol or ethanol. The addition of formulation ingredients resulted in little or no variation in mineralisation rate compared to an equivalent application volume of methanol/water.  相似文献   
110.
Callus produced from leaves of a Ghanaian strain of the neem tree, Azadirachta indica A. Juss has been shown to produce the natural insecticide azadirachtin when grown in a defined medium. The azadirachtin was isolated by standard procedures of solvent partition and column chromatography monitored by supercritical fluid chromatography. Biological activity was monitored with antifeedant tests using the desert locust (Schistocerca gregaria Forsk.). The azadirachtin was identified by chromatography on three independent chromatographic systems (SFC, HPLC & TLC) and two thin-layer colour tests. It has 100% antifeedant activity at < 0.04mg litre?1. The yield of azadirachtin was 0.0007% based on dry weight of callus.  相似文献   
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