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971.
不同控释氮肥运筹对粳稻养分吸收与氮素利用的影响 总被引:1,自引:0,他引:1
以绥粳18为供试材料,通过盆栽试验,在一次性施入控释氮肥免追肥条件下,设置不同施肥量(高、中、低、无)和施肥深度(5 cm、10 cm),探讨不同氮肥施用方式对粳稻养分吸收和氮素利用的影响。结果表明,在不同氮肥运筹条件下,粳稻各生育期氮、磷、钾的吸收、转运均存在明显的协同效应,施肥深度5 cm组,随着氮肥施用量的增加,粳稻的氮吸收总量增加,同时可促进磷的吸收,但影响幅度较小。钾变化与氮、磷变化有所不同。施肥深度10cm组,施高量氮肥抑制了粳稻对磷的吸收、减少了对氮的吸收,但有利于提高氮素利用率,对钾的吸收无显著影响。施用树脂包膜控释肥,纯氮用量为153 kg/hm^2、施肥深度5 cm、一次性施肥免追肥可获得最优水稻氮素利用效率并显著提高磷钾肥利用效率。 相似文献
972.
为探讨土壤Pb污染的治理方法,通过盆栽试验,比较了离子交换纤维的两种不同放置方式(分层放置与混匀放置)对麦田土壤Pb污染的修复效果。结果表明,在土壤1 000 mg·kg~(-1) Pb污染水平下,Pb污染处理(T1:Pb胁迫;T2:Pb+在土壤中分三层放置纤维;T3:Pb+在土壤中混匀剪碎的纤维)的土壤pH值、总有机碳含量较对照(CK:未添加Pb和离子交换纤维)有所降低。在小麦成熟期,T2、T3处理下土壤和植株各部位的Pb含量均低于T1处理,其中T3处理变化显著;T2、T3处理中纤维吸附的Pb含量则分别达到115.01和128.26 mg·kg~(-1)。T2、T3处理的Pb富集系数低于T1处理及CK。由此说明,离子交换纤维能够有效吸附土壤中的Pb,降低Pb从土壤向植株的转运能力,且离子交换纤维混匀放置方式的修复效果较好。 相似文献
973.
定量分析夏玉米同一品种产量及产量构成要素时空变化,探讨造成产量时空差异的气候年型组合变化特征。基于2004~2013年夏玉米种植区郑单958多点田间试验数据分析表明,夏玉米区域平均产量为9 055 kg/hm~2,年际差为1 635 kg/hm~2,变幅为18.1%;地点差4 258 kg/hm~2,变幅为47.1%。夏玉米区域平均千粒重为313 g,年际变幅为13.1%;地点变幅为27.8%。夏玉米区域平均穗粒数为479,年际变幅为18.0%,地点变幅为38.7%。千粒重的增加导致夏玉米产量显著增加。穗粒数显著降低和时空差异大是造成产量波动和时空差异变幅大的主要原因。夏玉米产量和产量构成要素,低产点受各气候要素变化的影响显著;平产点受温度和日最高温度大于33℃的天数影响显著;高产点受降水影响显著。 相似文献
974.
AIMTo investigate the roles of protein phosphatase 4 (PP4) in down-regulation of endothelial nitric oxide synthase (eNOS) Ser633 phosphorylation induced by palmitic acid (PA). METHODSHuman umbilical vein endothelial cells (HUVECs) were treated with PA at 25 μmol/L, 50 μmol/L, 100 μmol/L and 200μmol/L for 36 h, or treated with PA at 100 μmol/L for 12 h, 24 h, 36 h and 48 h. Protein phosphatase 2A (PP2A) family inhibitor fostriecin (FST, 20 nmol/L) or okadaic acid (OA, 5 nmol/L) was selected to pretreat the HUVECs for 30 min. Protein phosphatase 4 catalytic subunit (PP4c) siRNA or protein phosphatase 2A catalytic subunit (PP2Ac) siRNA was transfected into the HUVECs. The protein expression levels of of eNOS, PP4c and PP2Ac, as well as the level of eNOS Ser633 phosphorylation, were detected by Western blot. The intracellular nitric oxide (NO) content was measured by DAF-FM DA. RESULTS(1) Compared with control group, the levels of eNOS Ser633 phosphorylation were decreased in PA groups in which the HUVECs were treated with 25 μmol/L, 50 μmol/L, 100 μmol/L and 200 μmol/L PA for 36 h (P< 0.05) and 100 μmol/L PA for 24 h, 36 h and 48 h (P< 0.05). No significant difference in the level of total eNOS protein expression among all the groups was observed. (2) Compared with control group, both FST and OA pretreatment reversed the reduction of eNOS Ser633 phosphorylation (P< 0.05) and the decrease in intracellular NO content (P< 0.05) induced by PA. No significant difference in the level of total eNOS protein expression among all the groups was observed. (3) Compared with si-Control group, the PP4c protein expression was significantly reduced (P< 0.05), while the level of eNOS Ser633 phosphorylation was significantly increased in si-PP4c group (P< 0.05). Although the levels of PP2Ac protein expression declined significantly (P< 0.05), the level of eNOS Ser633 phosphorylation remained unchanged in si-PP2Ac group. No significant differencein the level of total eNOS protein expression among all the groups was found. CONCLUSION PA significantly reduces the level of eNOS Ser633 phosphorylation and the content of NO in the HUVECs, which may be due to PA inducing the activation of the PP2A family member PP4 rather than PP2A. 相似文献
975.
AIM: To study the effects of apelin-13 on oxidative stress induced by high uric acid in 3T3-L1 adipocytes and its underlying mechanisms. METHODS: 3T3-L1 adipocytes were stimulated with uric acid at 10 mg/dL for 48 h. Some of the adipocytes were administered with 1 μmol/L apelin-13 in the presence of uric acid at 10 mg/dL. The adipocytes stimulated with 100 μmol/L H2O2 were served as positive controls. The intracellular reactive oxygen species (ROS) concentrations were detected by flow cytometry. The biochemical kits were used to measure the activities of superotide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and NADPH oxidase (NOX) activity, and the content of malondialdehyde (MDA) in the cell lysate and the supernatant. The mRNA levels of renin-angiotensin system (RAS) components, including angiotensinogen (AGT), angiotensin-converting enzyrne1 (ACE1), angiotensin II type 1 receptor (AT1R) and AT2R, as well as angiotensin II receptor -like 1 (APJ) were measured by real-time PCR. The concentrations of angiotensin II (AngⅡ) in the cell lysate and the supernatant were measured by ELISA. RESULTS: Adipocytes stimulated with uric acid at 10 mg/dL had lower activities of antioxidant enzymes (SOD, GSH-PX and CAT) and higher levels of NOX activity and MDA content (P < 0.05). Accordingly, the intracellular ROS levels were found to be dramatically increased. However, apelin-13 administration attenuated uric acid-induced oxidative stress in the 3T3-L1 adipocytes. Uric acid at 10 mg/dL upregulated the mRNA expression of local RAS, enhanced AngⅡ concentrations both in the cell lysate and the supernatant, and down-regulated the mRNA level of APJ in the adipocytes (P < 0.05). Conversely, apelin-13 partially reversed these parameters. CONCLUSION: Apelin-13 attenuates oxidative stress induced by uric acid, may be via down-regulation of local RAS expression in the 3T3-L1 adipocytes. 相似文献
976.
Epithelial sodium channel (ENaC) is an ion channel widely distributed in various tissues and organs of human. It is composed of 3 homologous subunits and allows the flow of sodium ion across epithelial cells, maintain?ing water-salt balance in the cells. Recent studies show that abnormal expression or dysfunction of ENaC in the respiratory system affects water-salt balance, fluid transportation and cell mobility, and causes abnormal changes of the airway surface liquid level and impaired clearance. ENaC is closely related to the development of respiratory diseases, such as cystic fibrosis, asthma and chronic obstructive pulmonary disease. This article reviews the progress in ENaC structure, function and roles in related respiratory diseases in order to provide a reference for the treatment of the diseases. 相似文献
977.
入侵杂草刺萼龙葵Solanum rostratum Dunal传播扩散的主要载体是种子,研究其种子休眠萌发基因的激素调控对于其防除具有重要意义,而选择合适的内参基因可以提高相关基因表达分析的准确性。本研究以赤霉素、脱落酸和水处理的刺萼龙葵种子为材料,利用geNorm、NormFinder、BestKeeper和RefFinder 4种软件对15个候选内参基因进行表达稳定性评价,并通过检测ABI5(abscisic acid-insensitive 5)的表达验证所筛选的内参基因的适用性。结果表明,对于赤霉素、脱落酸和水处理过的种子,最稳定的内参基因分别为eIF(eukaryotic initiation factor)、SAND(SAND protein family)和ACT(β-actin);对所有种子样本而言,PP2Acs(a catalytic subunit of protein phosphatase 2A)是最稳定的内参基因。研究结果将为刺萼龙葵种子休眠萌发的遗传调控研究提供重要参考。 相似文献
978.
正雀麦花叶病毒(brome mosaic virus,BMV)为正义单链RNA病毒。BMV寄主范围广泛,在波兰等地均有发现(Trzmiel et al.,2015),大多危害禾本科、豆科、茄科等植物,感病植株常表现出褪绿、轻微花叶症状。因此,为减轻BMV造成的经济损失和丰富BMV的检测方式,本研究拟构建BMV的外壳蛋白(coat protein,CP)基因的原核表达载体,在大肠杆菌Escherichia coli中表达BMV的外壳蛋白,制备高特异性和高灵敏度的抗血清,以期用于BMV的有 相似文献
979.
为了明确微波辐照对全麦粉储藏稳定性及品质的影响,通过对全麦粉进行不同微波功率和不同微波时间处理,分析了全麦粉储藏过程中菌落总数以及脂肪酸值、面团流变学特性和馒头品质的变化。结果表明,随着微波功率的增加和处理时间的延长,全麦粉脂肪酸值和菌落总数增加速率得到抑制;湿面筋含量、面团稳定时间先增加后降低;气体释放曲线的最大高度(H′_m)和产气量(R_1)逐渐增加,气体保留体积(R_2)先增加后降低,发酵性能得到改善;馒头比体积与综合评分先增加后降低。当微波辐照功率为400 W、处理时间为120 s时,全麦粉可以更好储藏,同时全麦粉面团的粉质特性、流变发酵特性及馒头的品质得到改善。 相似文献
980.
利用碾皮设备对小麦进行碾皮处理,对比普通小麦粉和不同碾皮时间下的全麦粉农药残留量、呕吐毒素含量、含砂量、干湿面筋含量、粉质特性、流变发酵特性、淀粉糊化特性以及馒头的品质指标来研究碾皮技术对全麦粉及馒头品质的影响。结果表明,随着碾皮时间的延长,小麦碾皮率逐渐升高,全麦粉中的农药残留量、呕吐毒素含量和含砂量呈现下降趋势;全麦粉精度和亮度增大,干湿面筋含量逐渐降低,但始终高于普通小麦粉,弱化度总体呈现下降趋势,全麦粉面团产气量和持气量呈现先增加后减小趋势,并在碾皮时间为20 s时达到最大,淀粉糊化特性总体呈增加趋势;全麦馒头的亮度、比容随着碾皮时间的延长逐渐升高,其感官评分在碾皮时间为20 s时最高。综上所述,碾皮处理在一定程度上提升了全麦粉和馒头的品质,碾皮时间为20 s时,全麦粉及其馒头的各项安全指标和品质特性均处于最佳状态。 相似文献