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利用同源克隆技术和cDNA末端快速扩增(RACE)技术克隆大黄鱼胞质型磷脂酶A2(cPLA2)基因的cDNA全长.此外,应用实时定量PCR法检测不同日龄大黄鱼仔稚鱼cPLA2基因的表达量.序列分析结果表明:cPLA2基因全长2 550 bp(GenBank登录号:KF006240.1),其中5'端非编码区176 bp,开放阅读框2 169 bp,3'端非编码区205 bp,共编码723个氨基酸.系统进化树分析结果表明:克隆所得大黄鱼cPLA2基因与其他鱼类的cPLA2基因亲缘关系较近,与哺乳动物的亲缘关系较远.定量检测结果表明:大黄鱼仔稚鱼cPLA2基因的表达量随日龄的增加为先显著升高(1、3、7日龄vs.15日龄,P<0.05),在15日龄时达到最高值,随后显著下降(15日龄vs.19日龄,P<0.05),之后趋于平稳.由此可知,大黄鱼从仔稚鱼到幼鱼早期的变形过程中,磷脂分解代谢的关键酶cPLA2基因的表达量呈现有规律的变化,这可能对机体保持体内磷脂的动态平衡、维护细胞膜的流动性具有重要的意义.大黄鱼仔稚鱼cPLA2基因表达量的变化趋势在一定程度上可以衡量大黄鱼消化系统的发育情况. 相似文献
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在江门市林科所苗圃选择不同粗细度、不同萌芽度的降香黄檀插条进行扦插繁殖试验,每10 d进行1次成活率调查。结果表明:插条的萌芽度和粗细度均极显著影响扦插的成活率,萌芽度和粗细度的交互作用对扦插的成活率也有极显著影响;未萌芽插条扦插成活率明极显高于已萌芽插条的扦插成活率;3种粗细度的枝条中以粗细度为0.7~1.2 cm的插条扦插成活率最高;在枝条萌芽度及粗细度交互作用下,粗细度为0.7~1.2 cm的未萌芽插条扦插成活率最高,粗细度小于0.7 cm的已萌芽插条扦插成活率最低。 相似文献
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为评价珠三角河网初级生产力,于2015年3月、6月、9月、12月对其进行取样调查,采用多元统计方法研究初级生产力时空差异及其与环境因素关系。结果表明,珠三角河网初级生产力(碳,C)为98.81~927.21mg·(m~2·d)~(-1),均值为346.51 mg·(m~2·d)~(-1)。调查区域初级生产力季节变化明显,总体上表现为春季冬季夏季秋季。各站位初级生产力均值以珠江桥站位最高[600.61 mg·(m~2·d)~(-1)],市桥站位最低[232.60 mg·(m~2·d)~(-1)]。初级生产力与透明度、氮磷营养盐、叶绿素a呈正相关关系(P0.01,n=52),与硅酸盐呈负相关关系(P0.01,n=52),与水体富营养化综合指数(EI)呈线性相关关系。珠三角河网以中营养、富营养为主体,与其他水域相比,初级生产力较低,污染程度较严重,需防止其向富养化发展。 相似文献
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为从土壤中筛选能够同时降解单宁和植酸的微生物,本实验利用富集培养技术,分离、筛选、鉴定土壤中的单宁和植酸降解菌,并研究其在液态发酵下的产酶能力。结果显示,从土壤中共获得109株纯菌落,包括39株细菌、46株酵母菌以及24株霉菌。分别用单宁筛选性培养基和植酸筛选性培养基筛选上述菌株,获得27株植酸降解菌和14株单宁降解菌,其中霉菌M-6、M-3和M-1可以同时分解单宁和植酸,且霉菌M-6的水解圈直径大于M-3和M-1。在液态发酵条件下,随着发酵温度的升高(20~35°C),霉菌M-6产单宁酶和植酸酶的活力呈现先升高而后降低的趋势,在发酵温度为30°C时达到最高值(P0.05)。随着发酵p H的升高(p H 4~7),霉菌M-6产单宁酶和植酸酶的活力呈先升高后降低的趋势(P0.05);其中单宁酶活力在发酵p H值为5时达到最高值,显著高于其他处理组(P0.05);而植酸酶活力在发酵p H值为5时达到最高值,显著高于发酵p H 4和7处理组(P0.05),但与发酵p H 6处理组差异不显著(P0.05)。通过菌落和菌株形态学以及分子测序方法,鉴定M-6为黑曲霉。因此,本研究从土壤中分离筛选出3株(M-6、M-3和M-1)能够同时水解单宁和植酸的降解菌,在液态发酵条件下,黑曲霉M-6产单宁酶和植酸酶的最佳发酵温度为30°C,最佳发酵p H值为5。 相似文献
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TAN Wei-ping XIA Yan WU Bao-jing LI Jing HUANG Hua-rong HUANG Shao-liang MAI Xian-di 《园艺学报》2009,25(12):2399-2402
AIM: To investigate the effect of T-bet plasmid gene transfer to airway on allergen induced airway inflammation in a murine asthmatic model. METHODS: A mouse asthma model was established by sensitization with ovalbumin (OVA). Forty C57BL/6 mice were divided into 4 groups (10 mice in each group): the normal control group (group A), the asthmatic model group (group B), the pcDNA3 plasmid group (group C), and the pcDNA3-T-bet group (group D). The animals in group B, C and D were sensitized and challenged with OVA. The animals in group A were applied with normal saline. pcDNA3 plasmid at dose of 50 μg was intranasally administered at 24 h before intranasal challenges to the mice in group C, and the 50 μg pcDNA3-T-bet plasmid for the mice in group D. Bronchial alveolar lavage fluid (BALF) was collected and lung tissues were resected at 48 h after OVA challenge for later assay. RESULTS: After administration with pcDNA3-T-bet plasmid, high level of T-bet expression at 48 h was detected in the lung tissue by Western blotting. In pcDNA3-T-bet treated asthmatic models, histological evaluation revealed the significant suppression of eosinophil peribronchial and perivascular infiltration, and reduction of epithelial damage. The numbers of eosinophils, neutrophils and lymphocytes in BALF from pcDNA3-T-bet treated mice were significantly reduced compared to those in asthmatic control group (P<0.05). The level of IL-4 in BALF was significantly decreased in pcDNA3-T-bet group compared to that in asthmatic control group (P<0.05), while the level of IFN-γ in BALF was significantly increased in pcDNA3-T-bet group. No significant change of inflammation cells and cytokines in pcDNA3 plasmid group and asthmatic control group was observed (P>0.05). CONCLUSION: Intranasal pcDNA3-T-bet plasmid transfer inhibits asthmatic airway inflammation in the murine asthmatic model, suggesting a new therapeutic strategy for allergic asthma. 相似文献
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A 10‐week feeding experiment was conducted to evaluate the effect of different protein to energy ratios on growth and body composition of juvenile Litopenaeus vannamei (initial average weight of 0.09 ± 0.002 g, mean ± SE). Twelve practical test diets were formulated to contain four protein levels (300, 340, 380 and 420 g kg?1) and three lipid levels (50, 75 and 100 g kg?1). Each diet was randomly fed to triplicate groups of 30 shrimps per tank (260 L). The water temperature was 28.5 ± 2 °C and the salinity was 28 ± 1 g L?1 during the experimental period. The results showed that the growth was significantly (P < 0.05) affected by dietary treatments. Shrimps fed the diets containing 300 g kg?1 protein showed the poorest growth. However, shrimp fed the 75 g kg?1 lipid diets had only slightly higher growth than that fed 50 g kg?1 lipid diets at the same dietary protein level, and even a little decline in growth with the further increase of dietary lipid to 100 g kg?1. Shrimp fed the diet with 420 g kg?1protein and 75 g kg?1 lipid had the highest specific growth rate. However, shrimp fed the diet with 340 g kg?1 protein and 75 g kg?1 lipid showed comparable growth, and had the highest protein efficiency ratio, energy retention and feed efficiency ratio among dietary treatments. Triglycerides and total cholesterol in the serum of shrimp increased with increasing dietary lipid level at the same dietary protein level. Body lipid and energy increased with increasing dietary lipid level irrespective of dietary protein. Results of the present study showed that the diet containing 340 g kg?1 protein and 75 g kg?1 lipid with digestible protein/digestible energy of 21.1 mg kJ?1 is optimum for L. vannamei, and the increase of dietary lipid level has not efficient protein‐sparing effect. 相似文献
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