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1.
2017年引进早熟杂柑品种‘爱媛28’香橙砧和枳砧苗分别在大棚设施和露天进行试种,栽培4年调查比较两个砧木组合的生长表现、丰产性与果实品质,结果表明:‘爱媛28’香橙砧树表现生长势强,冠幅、树高、茎粗、结果枝、秋梢等生长量指标显著大于枳砧树,3a树初产1436 kg/667㎡,4a树2523kg/667㎡,显著高于枳砧4a树初产1809kg/667㎡;大棚种植香橙砧4a树果实10月下旬TSS11-12%,12月中旬TSS可达15%,与枳砧相当,可滴定酸比枳砧略高,两者固酸比均达18以上,口感风味极佳,两者单果重、果形指数、果皮厚度、可食率无显著性差异;未密封大棚4a树体经受2020年寒冬极端低温考验无明显冻害,抗旱抗寒能力中等,易感黑点病和流胶病,大棚种植能很好预防黑点病。综合评价爱媛28枳砧和香橙砧均适合在南平市种植,香橙砧比枳砧早期丰产性稳产性好,收益更高,香橙砧‘爱媛28’设施种植较枳砧更具优势。  相似文献   
2.
AIM: To investigate the inhibitory effect of microRNA-145 (miR-145) on epithelial-mesenchymal transition (EMT) in renal cancer A-498 cells. METHODS: The A-498 cells were transfected with miR-145 mimics (M145) and mimic negative control(MNC), which served as M145 group and MNC group, respectively. Mock control (MC) group was set up using untreated A-498 cells. The expression level of miR-145 in each group was detected by RT-qPCR. Transwell assay was used to detect the invasion ability of the cells. The protein expression of vimentin, E-cadherin and ADAM28 was determined by Western blot. Bioinformatic method was used to predict the target genes of miR-145. Antagonistic effect of ADAM28 over-expression on the inhibition of EMT by miR-145 was detected by Western blot. The relationship between miR-145 and ADAM28 was analyzed by dual-luciferase reporter assay. RESULTS: The expression level of miR-145 in M145 group was significantly up-regulated than that in MC group (P<0.05). The number of invasive cells in M145 group was 12.78±3.37, which was significantly lower than that in MC group (P<0.05). ADAM28 may be the target gene of miR-145. Compared with MC group, the protein expression of vimentin and ADAM28 in M145 group was significantly decreased (P<0.05), while the protein expression of E-cadherin was significantly increased (P<0.05).After ADAM28 over-expression, the protein expression of vimentin in the A-498 cells of M145 group was significantly increased (P<0.05), and the protein expression of E-cadherin was significantly decreased (P<0.05). The results of dual-lucife-irasei reporter assay showed that ADAM28 was a downstream target gene of miR-145. CONCLUSION: miR-145 may inhibit the expression of EMT-related proteins through the downstream target gene ADAM28 and inhibit the EMT process of renal cancer A-498 cells.  相似文献   
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Both morphological characters and a portion of of 28S rDNA sequences were used to identifying Tomicus species.The specimens were classed into groups with the following characters: 1) granules or punctures on interstria 2 on the declivity of the elytra;2) length of the elytral interstrial hairs and hairs arising from punctures;3) arrangement of pronotal punctures and hairs.These characters could be clearly examined under a binocular microscope at 30×magnification and they were applicable and valuable for the forest entomologists to identify Tomicus species.The phylogenetic tree established with difference in 28S rDNA sequence of D2 region revealed that the specimens of each group identified by morphological characters were also grouped together.The genetic distances of intra-species, inter-species and inter-genus were not overlapped. Genetic divergence of 28S rDNA was also useful for identifying Tomicus species.  相似文献   
5.
28%苄嘧磺隆·二氯喹啉酸WP对水稻秧田杂草及产量的影响   总被引:1,自引:0,他引:1  
研究了28%苄嘧磺隆·二氯喹啉酸对水稻秧田稗草[Echinochloa crusgalli (L.) Beauv.]、鸭舌草[Monochoia vaginalis(Burm.f.)]等的防除效果,并测定了杂草对氮、磷、钾和水分的影响以及对水稻产量的影响.结果表明,28%苄嘧磺隆·二氯喹啉酸WP对水稻秧田的主要杂草具有良好的防治效果,有效成分用量为168~420 g/hm2的28%苄嘧磺隆·二氯喹啉酸对水稻秧田稗草密度防效和鲜重防效分别为84.06%~98.50%、91.55%~98.63%,对鸭舌草的密度防效和鲜重防效分别为94.06%~100.00%、90.94%~100.00%,显著优于对照药剂10%苄嘧磺隆WP和50%二氯喹啉酸WP.28%苄嘧磺隆·二氯喹啉酸施用后,增产效果总体优于对照药剂,在水稻秧田具有良好的推广前景.  相似文献   
6.
津原E-28常规粳稻品种,在天津稻区全生育期177d左右,株高117.3cm,穗长22.0cm,千粒重30.2g,对稻曲病、条纹叶枯病表现高抗(HR),稻瘟病表现中抗(MR)。抗早衰,茎秆粗壮坚韧,抗倒伏。后期活秆成熟。米质指标达到国标等级优1标准。适于机插秧新技术栽培。  相似文献   
7.
The roots of 20 days old seedlings of tomato (Lycopersicon esculentum Mill.) at the time of their transplantation, were dipped in 10−8, 10−7, 10−6 or 10−5 M of 28-homobrassinolide (HBR) for 15, 30 or 45 min and were allowed to grow in earthen pots, in a net house. The leaves of the plants, at days 30 and 60, possessed elevated quantities of nitrate reductase (NR), carbonic anhydrase (CA) and the contents of chlorophyll. The values for all the above characteristics were significantly higher than that of the water-fed control. The fruits borned at the treated plants were more in number and possessed a lower quantity of ascorbic acid than the control. Moreover, the fruits at ripening, had higher levels of lycopene and β-carotene. Among the treatments, 15 min feeding of 10−8 M HBR proved best.  相似文献   
8.
Global distribution of platyhelminth parasites and their host specificities are not well known. Our hypothesis was that platyhelminth parasites of large pelagic fishes are common around the world. We analysed molecular variation in three different taxa of platyhelminth parasites infecting four species of tunas: yellowfin tuna (Thunnus albacares, Scombridae) from Western Australia, southern bluefin tuna (Thunnus maccoyii, Scombridae) from South Australia, Pacific bluefin tuna (Thunnus orientalis, Scombridae) from Pacific Mexico and northern bluefin tuna (T. thynnus, Scombridae) from two localities in the Mediterranean (Spain and Croatia). Comparisons of ITS2 and partial 28S rDNA demonstrated two congeneric species of blood flukes (Digenea: Sanguinicolidae) from multiple hosts and localities: Cardicola forsteri from southern bluefin and northern bluefin tunas, and Cardicola sp. from Pacific bluefin and northern bluefin tunas; and a gill fluke, Hexostoma thynni (Polyopisthocotylea: Hexostomatidae), from yellowfin, southern bluefin and northern bluefin tunas. Partial 28S rDNA indicates that a second type of fluke on the gills, Capsala sp. (Monopisthocotylea: Capsalidae), occurs on both southern bluefin and Pacific bluefin tunas. This appears to be the first report of conspecific platyhelminth parasites of teleosts with a wide‐ranging geographical distribution that has been confirmed through molecular approaches. Given the brevity of the free‐living larval stage of both taxa of flukes on the gills (H. thynni and Capsala sp.), we conclude that the only feasible hypothesis for the cosmopolitan distribution of these flatworms is migrations of host tunas. Host migration also seems likely to be responsible for the widespread occurrence of the two species of blood flukes (Cardicola spp.), although it is also possible that these were translocated recently by the spread of infected intermediate hosts.  相似文献   
9.
对车用28V铁氧体永磁发电机进行了结构设计,确定出永磁体体积及发电机转子和定子的结构参数,设计了由基准电路、取样电路、触发电路等组成的三相半控桥式整流稳压电路,对设计的发电机及稳压电路进行了试验分析,验证了设计的合理性.  相似文献   
10.
ABSTRACT:   Paralytic shellfish poisoning (PSP) toxins produced by Alexandrium isolates from Korea were analyzed by high-pressure liquid chromography. Species designation of the regional isolates was determined by morphological criteria and ribotyping inferred from sequences of the 28S rDNA D1-D2 region. Toxin analysis performed at the exponential growth phase, revealed that the two strains of A. fraterculus were non-toxic, while the strains of A. tamarense and A. catenella were toxic. Toxic isolates DPC7 and DPC8 of A. catenella produced GTX1, 2, 3, 4, 5, dcGTX2, 3, C1, 2, neoSTX and STX with trace or non-detectable levels of C3 and C4, while isolates UL7, KDW981, SJW97043, SJW97046, KJC97111 and KJC97112 of A. tamarense produced GTX1, 2, 3, 4, dcGTX3, C1, 2, neoSTX with trace or non-detectable levels of C3, 4, dcSTX and STX, and no GTX5 and dcGTX2. The major toxins produced by A. catenella were C1 +2, and those of A. tamarense were C1 +2 and GTX4 in most of the isolates. A. tamarense strains other than SJW97046 produced a relatively high proportion of carbamate toxins, reflecting the high toxicity scores of shellfish intoxication in sampled coastal areas. Two representative toxic isolates, A. tamarense SJW97043 and A. catenella DPC7, were cultured for 30 days in batch mode and subjected to toxin analysis at 5-day intervals. Comparison of toxin productivity in terms of total toxin content, toxin components, and their variations with culture age revealed marked differences between the two strains.  相似文献   
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