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31.
The prevalence of strains of Staphylococcus aureus, coagulase-negative (CN) staphylococci, Listeria monocytogenes, Escherichia coli, Enterococcus faecalis, E. faecium and Bacillus cereus, was investigated in 111 bulk milk samples. Staphylococcus aureus was isolated from 38 samples, CN staphylococci from 63 samples, E. coli from 49 samples, E. faecalis or E. faecium from 107 samples, and L. monocytogenes from two samples. Bacillus cereus was not found in any of the samples and three samples were free of any of the selected species. Sensitivity to the anti-microbial drugs amikacin, ampicillin, ampicillin + sulbactam, cephalothin (CLT), cephotaxime, clindamycin, chloramphenicol (CMP), co-trimoxazole, erythromycin (ERY), gentamicin, neomycin, norfloxacin, oxacillin, penicillin, streptomycin (STR), tetracycline (TTC) and vancomycin was tested using the standard dilution technique. Minimum inhibitory concentration (MIC) characteristics (MIC50, MIC90, MIC range) were determined for each microbial species. Resistance against one or more anti-microbial drugs was found in 93% of S. aureus, 40% of CN staphylococci, 73% of E. coli, 88% of E.faecalis, 55% of E.faecium, and one L. monocytogenes strain. Most of the strains, particularly enterococci, were resistant to STR, TTC, and ERY (MIC50 4 microg/ml). A high percentage of staphylococci were resistant to beta-lactam antibiotics. High resistance to CLT was found in 11 strains of E. coli (MIC 256 microg/ml) and strains resistant to CMP (MIC90 16 microg/ml) were detected. The highest numbers of resistance phenotypes were found in E. coil (16) and CN staphylococci (12). Eighteen identical resistance phenotypes were demonstrated in indicator bacteria (E. coli, E. faecalis, E. faecium) and pathogens (S. aureus, CN staphylococci) isolated from the same bulk milk sample. The obtained resistance data were matched against the herd owners' information on therapeutic use of the drugs. This confrontation could not explain the findings of strains resistant to ERY or CMP. Our findings are evidence of selection of resistant strains among not only pathogenic agents, but also among indicator bacteria which can become significant carriers of transmissible resistance genes.  相似文献   
32.
本研究通过调查苏氨酸与赖氨酸的比率对猪生长性能、表观可消化能和血液尿素氮 (BUN)浓度的影响 , 估测生长阉公猪和小母猪所需最佳苏氨酸与赖氨酸的比率 . 试验采用 150头杂交猪 (长白×约克夏×杜洛克 , 平均体重为 16.75± 0.45 , 其中阉公猪 75头 , 小母猪 75头 ), 按 2× 3析因设计 , 随机分成 6个处理 阉公猪日粮含赖氨酸 1.12% , 按苏氨酸与赖氨 酸比率为 50% 、 60% 和 70% 分成 3个处理 小母猪日粮含赖氨酸 1.33% , 按苏氨酸与赖氨酸比 率为 50% 、 60% 和 70% 分成 3个处理 . 经整个试验期 (体重从 16至 56 ). 在平均日增重、平均 日采食量和饲料转化率方面 , 动物性别和苏氨酸与赖氨酸比率之间无相互影响 . 在生长性能 方面 , 有明显的性别影响 与小母猪相比 , 阉公猪表现出较好的生长性能 , 消耗较多的饲料 (P< 0.01)以及生长的较快 (P< 0.01). 随着苏氨酸与赖氨酸比率的增大 , 阉公猪的 ADG和 FCR有增加的倾向 , 但差异不显著 . 在除粗灰分 (CA)外的可消化性养分方面 , 动物性别和苏氨 酸与赖氨酸比率之间无相互影响 . 在性别之间 , 除小母猪对钙具有较高的可消化性 (P< 0.01)外 , 可消化性养分没有存在的差异 . 而日粮苏氨酸与赖氨酸比率对可消化性养分无影响 . 可消化性必需氨基酸 (EEA)、非必需氨基酸 (NEAA)和总氨基酸 (TTA)的平均值没有受到性别 和苏氨酸与赖氨酸比率的影响 . 没有发现性别和日粮中苏氨酸与赖氨酸比率相互影响的证据 . 在性别之间 , 小母猪的总 BUN浓度比阉公猪低 (P< 0.05). 可以得出结论 " 阉公猪日粮 (赖氨 酸水平为 1.12% )中 , 苏氨酸与赖氨酸比率为 70% , 小母猪日粮 (赖氨酸水平为 1.33% )中 , 苏 氨酸与赖氨酸比率为 60% , 较其它比率的苏氨酸与赖氨酸 , 分别获得较好的生长性能、养分 利用和较低的 BUN浓度 .  相似文献   
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35.
Reports on the internationally emerging significance of multiresistant zoonotic Salmonella in animals and man prompted studies to estimate the significance of multiresistant Salmonella enterica subspecies enterica serotype Typhimurium (S. Typhimurium) phage type DT104 of animal origin in Hungary. A collection of 231 strains (primarily of goose, turkey, poultry and porcine origin from the years 1997-1998) was tested for resistance against 7 selected antibiotics (ampicillin, chloramphenicol, enrofloxacin, nalidixic acid, streptomycin, tetracycline and sulphamethoxazole). Strains with resistance against 3 or more were defined as multiresistant. All strains were phage typed using Felix-Callow's S. Typhimurium phage typing system, and 91 of them (suspect DT104) were also typed according to Anderson's definitive typing (DT) system. In this study, 14% of animal strains from 1997-1998 was classified as DT104, for which turkey, pig and duck seemed to be the main carriers, and the multiresistant non-DT104 strains represented a further 6% of this collection. The prevalence of DT104 was highest among strains of turkey origin (50%), followed by strains of pig (29%), chicken (25%), duck (19%), and goose (3%) origin. The other DT104 related phage types (DT12 and U302) were only detected in the case of 4 strains (2 of porcine, and one each of turkey and of goose origin). The DT104 corresponded to the Felix-Callow types 2/3 or 2c/3 in each case, except in the case of 3 turkey strains where they corresponded to type 35/3. Nalidixic acid resistance was detected in all multiresistant turkey strains and in some of other animal origin but none of these strains were resistant to enrofloxacin. A retrospective analysis (based on the above relationship) indicated that S. Typhimurium strains corresponding to DT104 could be present and increase in the Hungarian farm animal population from about 2% to 20% between 1985 and 1990, in a manner similar to the emergence of human DT104, as reported elsewhere (Pászti et al., 2000). The 91 suspect DT104 strains were also tested for plasmid profile and for spvC gene indicating the presence of the large serotype specific plasmid (Ssp). No characteristic plasmid profile could be attributed to S. Typhimurium DT104. The serovar-specific large plasmid was detected by PCR for spvC in 100% of DT104 strains and in 77% of the non-DT104 strains. The virulence of two DT104 strains was tested in orally infected day-old chicks and compared with virulence of 4 non-DT104 strains. Higher colonizing virulence of DT104 strains could be established as compared to the other strains.  相似文献   
36.
Glycoprotein E-negative (gE–) laboratory strains of bovine herpesvirus 1 (BHV-1) were recently introduced as novel marker vaccines, allowing serological discrimination between vaccinated and naturally infected animals on the basis of lack or presence of antibodies against gE epitopes. The applicability of this approach is based on the genetic stability of the gE. However, mutant field variants of BHV-1 with a variable response in anti-gE ELISA have been isolated. The molecular characterization of a gE variant field isolate (Salwa strain) is presented here. By comparing the gE nucleotide and amino acid sequences of the Salwa strain with those of the wild strain Jura, ten mutated bases were found in the gE strain of Salwa, six of which alter the amino acid sequence, leading to changes in five amino acids. Both strains caused respiratory disease in experimentally infected calves, but Salwa generated slightly milder signs. Both viruses were excreted in nasal and ocular discharges, and were reactivated by dexamethasone treatment. In conclusion, the rather close similarities observed in the gE gene structure and pathogenicity features of the gE mutant and of the wild strain of BHV-1 confirm the genetic stability of gE. The findings indicate that the Salwa isolate is virulent, but less virulent than wild strains. Our data support the use of gE-negative marker vaccines in eradication programmes.  相似文献   
37.
Genetic typing of classical swine fever virus   总被引:18,自引:0,他引:18  
Three regions of the classical swine fever virus (CSFV) genome that have been widely sequenced were compared with respect to their ability to discriminate between isolates and to segregate viruses into genetic groups. Sequence data-sets were assembled for 55 CSFVs comprising 150 nucleotides of the 5' non-translated region, 190 nucleotides of the E2 envelope glycoprotein gene and 409 nucleotides of the NS5B polymerase gene. Phylogenetic analysis of each data-set revealed similar groups and subgroups. For closely related viruses, the more variable or larger data-sets gave better discrimination, and the most reliable classification was obtained with sequence data from the NS5B region. No evidence was found for intertypic recombination between CSFVs. A larger data-set was also analysed comprising 190 nucleotides of E2 sequence from 100 CSFVs from different parts of the world, in order to assess the extent and global distribution of CSFV diversity. Additional groups of CSFV are evident from Asia and the nomenclature of Lowings et al. (1996) [Lowings, P., Ibata, G., Needham, J., Paton, D., 1996. J. Gen. Virol. 77, 1311-1321] needs to be updated to accommodate these. A tentative assignment, adapting rather than overturning the previous nomenclature divides CSF viruses into three groups with three or four subgroups: 1.1, 1.2, 1.3; 2.1, 2.2, 2.3; 3.1, 3.2, 3.3, 3.4. The expanding data-base of CSFV sequences should improve the prospects of disease tracing in the future, and provide a basis for a standardised approach to ensure that results from different laboratories are comparable.  相似文献   
38.
To estimate the potency of a porcine parvovirus (PPV) vaccine, three vaccinated and three non-vaccinated pregnant gilts were infected with PPV and the distribution of the virus was studied in the tissues of their 51 fetuses. Virus detection was attempted using haemagglutination (HA) and immunofluorescence (IF) assays, as well as by standard (single) and nested polymerase chain reactions (PCR). None of the detection methods yielded positive results when used to test for the presence of virus in suspensions of organs from the fetuses from the vaccinated gilts. However, the virus was detected in the fetuses from non-vaccinated gilts as follows: HA was positive in 14 cases out of 23 (60.8%), IF in 16/23 (69.5%), standard PCR in 12/20 (60%), and the nested PCR in 19/23 (82.6%). Although the correlation among the results of various methods of virus detection was rather close (r<0.83), the sensitivity of the nested PCR was the highest, both when testing dilutions of PPV and when analysing the fetal organs. The nested PCR therefore provides a reliable approach for studies of virus distribution in fetal organs, with special reference to potency tests on vaccines.  相似文献   
39.
We studied changes in the parameters of the acid-base balance of the blood in cattle before animal transport to the slaughterhouses, after transport, after stunning and before bleeding. At the same time we studied the occurrence of DFD meat by measuring the pH value of the muscle and by determining the meat color. We found out that the disorder of acid-base balance was less manifest, with respect to the large capacity of the buffer systems of the blood, than the changes caused by glycogenolysis in the muscle.  相似文献   
40.
The percentual change in the content of pro-acrosin taking place in ram semen preserved for a short and long time was examined in the period from April to October. Two diluents for keeping semen at the temperature of 16 degrees C and one diluent for keeping semen at 3 to 4 degrees C were used in short-time preservation. The content of pro-acrosin was measured 2, 8 and 12 hours after dilution. The lactoso-yolk diluent and the diluent after Milovanov (1980) were used for cryopreservation. The content of pro-acrosin was examined before and after semen freezing. In short-time preservation, no statistically significant decrease of pro-acrosin content was demonstrated in the H Milch diluent (Peter, 1975) at the storage temperature of 16 degrees C and in the diluent after Milovanov (1980) at the temperature of 3 to 4 degrees C. In the diluent prepared after Milovanov (1980) a significant decrease of pro-acrosin content during preservation was recorded at the storage temperature of 16 degrees C. When the short-time preservation diluents were compared, significant differences in pro-acrosin content were found between them. In the long-time preservation diluents a significant difference in pro-acrosin content was found before and after semen freezing; the difference between the short- and long-time preservation diluents was also significant. A positive correlation was found between sperm activity and pro-acrosin content.  相似文献   
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