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51.
白斑综合征病毒与凡纳滨对虾肠道菌群区系之间关系的初步研究 总被引:9,自引:0,他引:9
比较了同一养殖池中的感染白斑综合征病毒(WSSV)和未感染WSSV的凡纳滨对虾的肠道菌群,旨在探讨对虾肠道菌群与机体健康状态之间的关系。感染WSSV对虾肠道的细菌总数为1.06×106CFU/尾,显著高于未感染WSSV的对虾(1.78×105CFU/尾;P<0.05),且其肠道中的细菌分别属于弧菌属、气单胞菌属、海水球菌属、盐水球菌属和乳酸杆菌属;染WSSV的对虾(P<0.05),气单胞菌的比例显著的低于感染WSSV的对虾(P<0.05);盐球菌所占的比例两者之间差异不显著。结果显示,两种对虾在肠道菌群组成和细菌组成和细菌数量上存在显著的差异,初步表明对虾肠道菌群区系和机体的健康状态密切相关。 相似文献
52.
宁康霉素对植物病原真菌的抑制作用 总被引:3,自引:0,他引:3
宁康霉素是由海洋细菌BAC-9912发酵获得的生物农药,对多种植物病原真菌有良好的抑制作用。本研究发现宁康霉素强烈抑制玉米纹枯病菌和苹果轮纹病菌的菌丝,可使玉米纹枯病菌菌丝枯萎和产生畸形。比较宁康霉素与农利灵和速克灵对玉米纹枯病菌的抑菌效果,结果显示宁康霉素的抑菌效果优于两种化学农药。 相似文献
53.
拮抗菌对香蕉枯萎病菌的抑菌作用初步研究 总被引:25,自引:1,他引:25
从土壤中分离到一株对香蕉枯萎病菌(Fusarium oxysporum f.sp.cubense)具有抑制作用的拮抗细菌--假单胞杆菌(Pseudomonas sp.),并对其抑菌效果、热稳定性以及作用机理进行了初步研究.结果表明,拮抗细菌发酵液及其无菌滤液对香蕉枯萎病菌的生长及其分生孢子的萌发具有显著的抑制作用(P<0.05),并导致病菌菌丝和分生孢子芽管扭曲、膨大;拮抗细菌发酵液经121℃处理30min后,对病菌生长的抑制作用降低. 相似文献
54.
Jian Li Jun-Hui Cheng Zhao-Jie Teng Xia Zhang Xiu-Lan Chen Mei-Ling Sun Jing-Ping Wang Yu-Zhong Zhang Jun-Mei Ding Xin-Min Tian Xi-Ying Zhang 《Marine drugs》2022,20(1)
Although the S8 family in the MEROPS database contains many peptidases, only a few S8 peptidases have been applied in the preparation of bioactive oligopeptides. Bovine bone collagen is a good source for preparing collagen oligopeptides, but has been so far rarely applied in collagen peptide preparation. Here, we characterized a novel S8 gelatinase, Aa2_1884, from marine bacterium Flocculibacter collagenilyticus SM1988T, and evaluated its potential application in the preparation of collagen oligopeptides from bovine bone collagen. Aa2_1884 is a multimodular S8 peptidase with a distinct domain architecture from other reported peptidases. The recombinant Aa2_1884 over-expressed in Escherichia coli showed high activity toward gelatin and denatured collagens, but no activity toward natural collagens, indicating that Aa2_1884 is a gelatinase. To evaluate the potential of Aa2_1884 in the preparation of collagen oligopeptides from bovine bone collagen, three enzymatic hydrolysis parameters, hydrolysis temperature, hydrolysis time and enzyme-substrate ratio (E/S), were optimized by single factor experiments, and the optimal hydrolysis conditions were determined to be reaction at 60 ℃ for 3 h with an E/S of 400 U/g. Under these conditions, the hydrolysis efficiency of bovine bone collagen by Aa2_1884 reached 95.3%. The resultant hydrolysate contained 97.8% peptides, in which peptides with a molecular weight lower than 1000 Da and 500 Da accounted for 55.1% and 39.5%, respectively, indicating that the hydrolysate was rich in oligopeptides. These results indicate that Aa2_1884 likely has a promising potential application in the preparation of collagen oligopeptide-rich hydrolysate from bovine bone collagen, which may provide a feasible way for the high-value utilization of bovine bone collagen. 相似文献
55.
Ni Pan Zi-Cheng Li Zhi-Hong Li Sen-Hua Chen Ming-Hua Jiang Han-Yan Yang Yao-Sheng Liu Rui Hu Yu-Wei Zeng Le-Hui Dai Lan Liu Guan-Lei Wang 《Marine drugs》2022,20(1)
Isaridin E, a cyclodepsipeptide isolated from the marine-derived fungus Amphichorda felina (syn. Beauveria felina) SYSU-MS7908, has been demonstrated to possess anti-inflammatory and insecticidal activities. Here, we first found that isaridin E concentration-dependently inhibited ADP-induced platelet aggregation, activation, and secretion in vitro, but did not affect collagen- or thrombin-induced platelet aggregation. Furthermore, isaridin E dose-dependently reduced thrombosis formation in an FeCl3-induced mouse carotid model without increasing the bleeding time. Mechanistically, isaridin E significantly decreased the ADP-mediated phosphorylation of PI3K and Akt. In conclusion, these results suggest that isaridin E exerts potent antithrombotic effects in vivo without increasing the risk of bleeding, which may be due to its important role in inhibiting ADP-induced platelet activation, secretion and aggregation via the PI3K/Akt pathways. 相似文献
56.
Anne-Sofie De Rop Jeltien Rombaut Thomas Willems Marilyn De Graeve Lynn Vanhaecke Paco Hulpiau Sofie L. De Maeseneire Maarten L. De Mol Wim K. Soetaert 《Marine drugs》2022,20(1)
The marine environment is an excellent resource for natural products with therapeutic potential. Its microbial inhabitants, often associated with other marine organisms, are specialized in the synthesis of bioactive secondary metabolites. Similar to their terrestrial counterparts, marine Actinobacteria are a prevalent source of these natural products. Here, we discuss 77 newly discovered alkaloids produced by such marine Actinobacteria between 2017 and mid-2021, as well as the strategies employed in their elucidation. While 12 different classes of alkaloids were unraveled, indoles, diketopiperazines, glutarimides, indolizidines, and pyrroles were most dominant. Discoveries were mainly based on experimental approaches where microbial extracts were analyzed in relation to novel compounds. Although such experimental procedures have proven useful in the past, the methodologies need adaptations to limit the chance of compound rediscovery. On the other hand, genome mining provides a different angle for natural product discovery. While the technology is still relatively young compared to experimental screening, significant improvement has been made in recent years. Together with synthetic biology tools, both genome mining and extract screening provide excellent opportunities for continued drug discovery from marine Actinobacteria. 相似文献
57.
58.
Sohee Kim Tu Cam Le Sang-Ah Han Prima F. Hillman Ahreum Hong Sunghoon Hwang Young Eun Du Hiyoung Kim Dong-Chan Oh Sun-Shin Cha Jihye Lee Sang-Jip Nam William Fenical 《Marine drugs》2022,20(1)
Analysis of the chemical components from the culture broth of the marine bacterium Saccharomonospora sp. CNQ-490 has yielded three novel compounds: saccharobisindole (1), neoasterric methyl ester (2), and 7-chloro-4(1H)-quinolone (3), in addition to acremonidine E (4), pinselin (5), penicitrinon A (6), and penicitrinon E (7). The chemical structures of the three novel compounds were elucidated by the interpretation of 1D, 2D nuclear magnetic resonance (NMR), and high-resolution mass spectrometry (HRMS) data. Compound 2 generated weak inhibition activity against Bacillus subtilis KCTC2441 and Staphylococcus aureus KCTC1927 at concentrations of 32 μg/mL and 64 μg/mL, respectively, whereas compounds 1 and 3 did not have any observable effects. In addition, compound 2 displayed weak anti-quorum sensing (QS) effects against S. aureus KCTC1927 and Micrococcus luteus SCO560. 相似文献
59.
针对宁夏银北地区大面积土壤盐碱化监测的需要,利用实测植被冠层光谱与Landsat 8 OLI影像相结合进行土壤含盐量和pH值估测研究.对实测植被冠层高光谱与影像多光谱反射率进行倒数、对数、三角函数及其一阶微分等一系列变换,确定最佳光谱变换形式,筛选敏感植被指数和敏感波段,分别建立基于实测植被光谱与Landsat 8 O... 相似文献
60.