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1.
本研究以大田葡萄品种‘梅鹿辄’为试材,采用大田喷施硅酸钾与室内低温处理相结合的方法,测定不同温度下葡萄叶片生理指标的变化,研究外源硅酸钾调控葡萄生理特性对低温胁迫的响应,探讨其提高葡萄抗寒性可能的作用机制。结果表明:低温胁迫下葡萄Inv活性被抑制,而其它指标则升高;喷施硅酸钾可显著降低低温胁迫下葡萄叶片的MDA含量,且当硅酸钾浓度为0.75%时对低温的损伤缓解作用最大;而脯氨酸、可溶性蛋白和可溶性糖含量、Inv、SPS活性及SS净活性均随硅酸钾浓度的升高而显著提高,但是可溶性蛋白含量在硅酸钾浓度为0.50%时最大,其它指标均在浓度为0.75%时最大;通过葡萄叶片各抗寒指标的隶属度值与综合评价指标看出,始花期0.75%的硅酸钾处理后葡萄抗寒性最强。综合分析,喷施硅酸钾可提高低温胁迫下葡萄叶片渗透调节物质含量,加快蔗糖转运及代谢速率,缓解活性氧累积,增强其耐寒性。  相似文献   
2.
The present study was designed to investigate the effects of diets containing advanced soy products (enzyme‐treated soy and fermented soy) or corn protein concentrate (CPC) in combination with porcine meal (PM) to completely replace poultry byproduct meal (PBM) on growth performance, body composition, and distal intestine histology of Florida pompano, Trachinotus carolinus. Four experimental diets were formulated to be isonitrogenous and isolipidic, to contain 400 g/kg crude protein and 80 g/kg lipid. A reference diet (PBM diet [PBMD]) contained 150 g/kg PBM and 495 g/kg soybean meal (SBM), and three test diets were formulated replacing PBM with 15 g/kg of CPC (CPC diet [CPCD]) or replacing all SBM and PBM with 535 g/kg fermented soy (fermented soybean meal diet [FSBMD]) or 451.3 g/kg enzyme‐treated soy (enzyme‐treated soybean meal diet [ESBMD]). All three test diets were supplemented with 38 g/kg of PM. Diets were fed based on a percentage of bodyweight adjusted after sampling the fish every 2 weeks to triplicate groups of Florida pompano juveniles (mean weight 8.06 ± 0.22 g). After 8 weeks of feeding, fish fed CPCD and ESBMD performed equally well in terms of final body weight, thermal growth coefficient, and percentage weight gain in comparison to fish fed PBMD. In all cases, feeding FSBMD resulted in poor feed conversion and lower feed intake compared to other treatments. Protein retention efficiency, whole‐body proximate composition, phosphorus, sulfur, potassium, magnesium, calcium, sodium, and zinc contents were not significantly influenced by the dietary treatments. The results obtained in the present histological study showed no significant differences in the thickness of serous layer, muscular layer, and submucosal layer of the intestine among treatments. Fish fed CPCD showed a significant widening of the lamina propria with an increase of cellular infiltration and higher presence of goblet cells compared to other dietary treatment. Based on these results, 451 g/kg ESBM or combination of 150 g/kg of CPC and 495 g/kg SBM supplemented with 38 g/kg PM can be utilized to develop a practical diet for juvenile Florida pompano without impacting growth, nutritive parameters, and several distal intestine health parameters.  相似文献   
3.
种植年限对设施蔬菜土壤养分和环境的影响   总被引:2,自引:0,他引:2  
为了给设施蔬菜地合理施肥提供依据,研究了不同种植年限设施蔬菜地土壤理化性质、微生物数量及酶活性变化,以露地土壤为对照(CK),采集种植1 a(年)、3 a、5 a、7 a、9 a、11 a、13 a、15 a、17 a、20 a以及20 a以上的0~20 cm设施蔬菜土壤样品,采用常规土壤理化性质检测方法测定了土壤理化性质和酶活性,采用平板计数法,分析土壤微生物数量。结果表明,设施菜地种植年限与土壤容重呈正相关,与土壤孔隙度呈负相关;设施菜地土壤pH值随种植年限的增加逐年降低,两者呈显著的负相关性;土壤EC值、土壤有机质和速效磷含量都随种植年限的增加而逐年增高,并与种植年限呈显著的正相关性;与CK相比,种植13 a的蔬菜样地土壤全氮和速效钾含量均显著地增加;连续种植20 a以上,设施蔬菜土壤含盐量比对照土壤显著地增加了486.49%。土壤细菌和放线菌数量、过氧化氢酶和碱性磷酸酶活性呈现出先增加后减少的趋势,且都在种植年限为11~13 a时达到最大;真菌数量随着种植年限的增加而增加,而土壤脲酶活性则随种植年限的增加呈下降趋势;转化酶活性随着种植年限的增加保持不变。土壤微生物数量与酶活性之间存在一定程度的相关关系,其中土壤真菌数量与土壤酶活性之间的相关性最为显著。综上所述,种植年限不同的设施菜地,土壤养分失衡,呈现酸化趋势,盐分含量逐年增加,土传真菌病害潜在发生,对设施蔬菜生产不利。  相似文献   
4.
[Objectives]To explore the inhibitory effect of AURKB gene in apoptosis and cancer cell growth in HCT 116 cells.[Methods]The in vitro cytology studies were carr...  相似文献   
5.
AIM: To observe the effect of beclin-1 silencing by the technique of RNA interference on the injury of human gastric cancer SGC-7901 cell by Sheliugu extract (the extract from tuber of Amorphophallus konjac, TuAKe). METHODS: To knock down the expression of beclin-1 gene, SGC-7901 cells were transfected with lentiviral vector carrying beclin-1-shRNA. The beclin-1 gene knock-down and non-knock-down SGC-7901 cells were treated with TuAKe. The cell viability was analyzed by CKK-8 assay. The percentages of apoptotic cells were detected by flow cytometry. The expression of beclin-1 and LC3 was detected by Western blot. RESULTS: The beclin-1 gene silencing decreased the protein expression of beclin-1 and increased the protein expression of LC3 in the SGC-7901 cells, leading to the decrease in cell viability and the increase in apoptotic rate (P<0.05). TuAKe increased the protein expression of beclin-1 and LC3 in the SGC-7901 cells, and decreased the protein expression of LC3 in the SGC-7901 cells with beclin-1 gene silencing, thus inhibiting the cell viability and increasing the apoptotic rate (P<0.05). CONCLUSION: Beclin-1 gene silencing inhibits the activation of beclin-1-related signaling pathway in gastric cancer SGC-7901 cells, and aggravates the injury of cell viability induced by TuAKe.  相似文献   
6.
AIM: To investigate the effect of microRNA-204 (miR-204) on the proliferation of Hodgkin lymphoma cells and the underlying mechanism. METHODS: The expression of miR-204 and Sirt1 mRNA in Hodgkin lymphoma tissues was detected by RT-qPCR. After transfection with miR-204 mimic, Sirt1 siRNA and miR-204 mimic+pcDNA3.1-Sirt1 into the L428 cells, the cell viability and BrdU incorporation were measured by CCK-8 assay and BrdU assay, respectively. The protein levels of Sirt1 and acetylated p53 (ac-p53) were determined by Western blot.The targeting relationship between miR-204 and Sirt1 was verified by double luciferase reporter assay. RESULTS: The low expression of miR-204 and the high mRNA expression of Sirt1 were found in the Hodgkin lymphoma tissues. Compared with control group, the cell viability, BrdU incorporation and the protein levels of Sirt1 and ac-p53 were significantly decreased after L428 cells were transfected with miR-204 mimic or Sirt1 siRNA (P<0.05). Compared with miR-204 mimic alone group, the cell viability, BrdU incorporation and the protein levels of Sirt1 and ac-p53 were increased after L428 cells were co-transfected with miR-204 mimic and pcDNA3.1-Sirt1 (P<0.05). The results of double luciferase reporter assay confiermed that Sirt1 was the target gene of miR-204. CONCLUSION: The inhibitory effect of miR-204 on the proliferation of L428 cells may be achieved by inhibiting the expression of Sirt1 and promoting the up-regulation of ac-p53.  相似文献   
7.
AIM:To investigate the effect of proline-spirooxindole on the viability and apoptosis of human non-small-cell lung cancer A549 cells. METHODS:The effect of proline-spirooxindole on the viability of A549 cells was determined by CCK-8 assay. The apoptosis was analyzed by flow cytometry. The effects of proline-spirooxindole on the expression of PARP and p53 and the phosphorylation of mTOR were determined by Western blot. RESULTS:After A549 cells were treated with proline-spirooxindole (25, 50 and 100 mg/L), the cell viability was decreased (P<0.01) compared with DMSO control group. The apoptotic rate was increased compared with DMSO control group (P<0.01). The protein expression of p53 was up-regulated, the increased apoptotic protein cleaved PARP was observed, and the phosphorylation of mTOR was inhibited (P<0.01). CONCLUSION:Proline-spirooxindole inhibits the viability of A549 cells and induces apoptosis, which may be related to the phosphorylation of mTOR.  相似文献   
8.
It was reported that the activity of NiR (nitrite reductase) enzyme encoded by the NiR gene was correlated with the regeneration ability in rice. To testify the function of NiR gene in bamboo, seven bamboo species whose calli had different differentiation rate were chosen to analyse their NiR enzyme activity. The results showed that bamboo NiR enzymatic activity had a certain correlation with the regeneration capacity. A NiR gene named DhNiR from Dendrocalamus hamiltonii with high regeneration capacity was cloned. Sequence analysis revealed that the ORF of DhNiR was 1779bp encoding 592 amino acids. Overexpression of DhNiR in rice reduced the time of shoot differentiation and increased the transformation rate, suggesting that DhNiR might play an important role in the regeneration ability of bamboo, and can be applied in regeneration and gene transformation of bamboo and other plant species.  相似文献   
9.
采用超声波结合复合酶液对高山油菜花粉进行破壁预处理后,以95%的乙醇提取花粉中黄酮,研究提取温度、时间和固液比对破壁高山油菜花粉黄酮得率的影响,筛选适宜的提取工艺。结果表明,超声波酶解处理时间60 min即可使油菜花粉破壁率达到90%以上;通过正交试验确定最佳提取工艺条件为:提取温度95 ℃,时间2 h,料液比1∶35 (g/mL),此时高山油菜花粉黄酮得率高达7.65%。  相似文献   
10.
The digestive tract of termite(Microcerotermes diversus) contains a variety of lignocellulose-degrading bacteria with exocellulases enzyme activity, not found in the rumen, which could potentially improve fiber degradation in the rumen. The objectives of the current study were to determine the effect of inoculation of rumen fluid(RF) with three species of bacteria isolated from termite digestive tract, Bacillus licheniformis, Ochrobactrum intermedium, and Microbacterium paludicola, on in vitro gas production(IVGP), fermentation parameters, nutrient disappearance, microbial populations, and hydrolytic enzyme activities with fibrous wheat straw(WS) and date leaf(DL) as incubation substrate. Inoculation of RF with either of three termite bacteria increased(P0.05) ammonia-N concentration compared with the control group(free of termite gut bacteria). Termite bacteria inoculation had no effect(P0.05) on gas production characteristics, dry matter, organic matter and neutral detergent fiber disappearance, pH, and concentration and composition of volatile fatty acids. Population of proteolytic bacteria and protozoa, but not cellulolytic bacteria, were increased(P0.05) when RF was inoculated with termite bacteria with both WS and DL substrates. Inoculation of RF with termite bacteria increased protease activity, while activities of carboxymethyl-cellulase, microcrystalline-cellulase, α-amylase and filter paper degrading activity remained unchanged(P0.05). Overall, the results of this study indicated that transferring lignocellulose-degrading bacteria, isolated from digestive tract of termite, to rumen liquid increased protozoa and proteolytic bacteria population and consequently increased protease activity and ammonia-N concentration in vitro, however, no effect on fermentation and fiber degradation parameters were detected. These results suggest that the termite bacteria might be rapidly lysed by the rumen microbes before beneficial effects on the rumen fermentation process could occur.  相似文献   
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