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991.
Jason W. Karl Jeffrey E. Herrick Dawn M. Browning 《Strength and Conditioning Journal》2012,65(6):638-646
Adapting what we currently know about ecosystems to a future where rangelands are changing is a new frontier in rangeland management. Current tools for knowledge discovery and application are limited because they cannot adequately judge ecological relevance of knowledge to specific situations. We propose development of integrated knowledge systems (KSs)—collections of resources (e.g., data, analytical tools, literature) drawn from disparate domains and organized around topics by process-based conceptual models. An integrated KS would define relevance by ecological attributes (e.g., soils, climate, vegetation) and location as a flexible mechanism for organizing, finding, and applying knowledge to rangeland management. A KS provides knowledge sources within a decision-making framework that defines what knowledge is needed and how it will be used to make decisions. Knowledge from a KS can identify appropriate spatial and temporal scales to address specific resource questions or objectives. Several factors currently limit KS development and implementation. These include limited interoperability of disparate information and knowledge systems; lack of consistent geographic referencing of knowledge; incomplete and inconsistent documentation of the origin, history and meaning of data and information; underexploited application of remote sensing products; limited ability to extrapolate and share local knowledge and unstructured information; and lack of training and education of professionals that can link ecological and technical fields of study. The proposed KS concept and recommendations present an opportunity to take advantage of emerging technologies and the collective knowledge of rangeland professionals to address changing ecosystems and evolving threats. If we keep on with a “business as usual” approach to finding and using information, we will struggle to meet our responsibilities as rangeland professionals. 相似文献
992.
Zetner K Schmidt H Pfeiffer S 《Veterinary therapeutics : research in applied veterinary medicine》2003,4(2):166-171
Concentrations of clindamycin in the mandible were determined in 17 dogs and 13 cats with severe plaque, gingivitis/periodontitis, and calculus that were treated orally with clindamycin (11 mg/kg) once daily for 5 days prior to professional teeth cleaning and extractions. The animals were patients at the Dental Department of the Clinic for Surgery and Ophthalmology of the University of Veterinary Medicine in Vienna, Austria. Clindamycin levels were determined during postextractional alveoloplasty. Approximately 1 to 3 mm3 of mandible was removed from the intraradicular septum in multirooted teeth and from the protruding labial/buccal alveolar rim with a small rongeur. The mean concentration of clindamycin was 8.18 microg/g in dogs (range=3.16 to 24.08 microg/g) and 17.43 microg/g in cats (range=2.45 to 51.60 microg/g). The concentration of clindamycin in the mandibles of dogs and cats may be useful to combat infections after periodontal procedures, tooth extractions, or injuries to the mandible. 相似文献
993.
Karl W. Mueller Wade O. Watanabe William D. Head 《Journal of the World Aquaculture Society》1992,23(3):199-204
Laboratory experiments were conducted to determine the effect of salinity on embryonic development and hatching in Neobenedenia melleni , a monogenean ectoparasite of seawater-cultured (37 ppt) Florida red tilapia ( Oreochromis urolepis hornorum × O. mossambicus ). Eggs, collected from adult monogeneans at 37 ppt, were exposed to different salinities (0, 6, 12, 18, 24, 30 and 37 ppt) for 48, 72 or 96 h. Varying degrees of post-treatment development and hatching occurred when natural seawater conditions were restored. Hatching success generally declined with decreasing salinity and increasing duration of exposure. Under all durations of exposure, hatching success remained relatively high (≥ 69.6%) at salinities of 24 ppt and above, but declined markedly (≤ 32.5%) at lower salinities. Hatching did not occur in eggs exposed to fresh water (0 ppt) for 72 and 96 h. The most effective treatments in preventing hatching, other than prolonged exposure to fresh water, were 96 h exposures to low-salinity brackish water. Percent hatch after 96 h exposure to 6, 12 and 18 ppt was 5.5, 11.9 and 5.8%, respectively. 相似文献
994.
Karl Enigk 《Journal of pest science》1957,30(3):33-34
Ohne Zusammenfassung 相似文献
995.
Evidence for the Colonization of Lactic Acid Bacteria in the Gastrointestinal Tract of Suckling Mink
Lactic acid bacteria are considered indigenous members of the gastrointestinal microflora in a number of animal species (Savage 1977a). Some intestinal strains of lactobacilli and streptococci are aWe to adhere to stratified squamous epithelium of some animals (Tannock et al. 1987), in the non-secreting part of the stomach of piglets (Barrow et al. 1980, Fuller et al. 1978) and rodents (Tannock et al. 1982), and in the crop of poultry (Fuller 1978). The presence of lactic acid bacteria in the digestive tract is believed to be of beneficial value to the host animal (Fuller 1989). The production of organic acids in the stomach or the crop helps maintaining a low pH which may be important for inhibiting the colonization of potentially pathogenic bacteria, particularly in the newborn animal (Barrow et al 1980, Fuller 1977, Fuller 1978). The adhesion of lactobacilli to squamous epithelium is host specific: strains capable of adhering to the epithelium of piglets are usually not able to adhere in rodents or poultry and vice versa (Fuller 1978, Lin & Savage 1984, Tannock et al 1982). Adhesion of lactic acid bacterial strains to other epithelia than stratified squamous epithelium has been reported. Thus, the attachment of lactobacilli to cells from the secreting epithelium of the murine stomach (Kotarski & Savage 1979), to intestinal cells of humans (Goldin & Gorbach 1987), and to columnar epithelial cells of piglets and calves (Mäyrä-Mäkinen et al 1983) has been demonstrated using in vitro methods. In another study the in vivo attachment of Enterococcus faecium to duodenal epithelium of gnotobi-otic chickens was demonstrated (Fuller et al 1981). Recent research indicated that in adult mink lactic acid bacteria are not indigenous members of the intestinal flora, and they do not attach to epithelium in any part of the gastrointestinal tract (Federsen & Jørgensen 1992). The present paper presents evidence that Gram positive cocci may colonize the gut of suckling mink kits and attach to the gut mucosa. 相似文献
996.
Development of a diagnostic PCR assay based on novel DNA sequences for the detection of Mycoplasma suis (Eperythrozoon suis) in porcine blood 总被引:34,自引:0,他引:34
An efficient method of control of porcine eperythrozoonosis (PE) caused by Mycoplasma suis is eradication of infection by detection and removal of infected carrier animals. At present, only a few tests are available for the diagnosis of these latent M. suis infections in pigs. The objective of this study was to develop a PCR assay based on novel DNA sequences for the identification of M. suis-infected pigs. A 1.8 kb EcoRI DNA fragment of the M. suis genome was isolated from the blood of pigs experimentally infected with M. suis. Specificity of the DNA fragment was confirmed by DNA sequence analysis and PCR using primers directed against sequences contained in the 1.8 kb fragment. PCR products of 782 bp in size were amplified only from M. suis particles prepared from the blood of experimentally infected pigs but not from any controls, comprising blood from gnotobiotic piglets and a panel of bacteria including other porcine mycoplasmas. PCR results were confirmed by dot blot hybridisation. The applicability of the PCR assay to diagnose M. suis infections in pigs was evaluated by investigating blood samples from 10 symptomatic pigs with clinical signs typical of porcine eperythrozoonosis and blood samples from 10 healthy pigs. The M. suis-specific PCR product was amplified from all samples taken at episodes of acute disease as well as from samples taken during the latent stage of infection, thus demonstrating the suitability of the PCR assay for detecting latent infected carrier animals. 相似文献
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