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71.
With diminishing world reserves of phosphorus (P) deposits and rising fertilizer prices, it is important to find alternate sources of P for crops. The aim of this research was to evaluate the effect of four different composts C1 (animal manure and straw), C2 (garden waste), C3 (wood chips and bark), and C4 (kitchen waste) on soil P pools and P uptake by wheat on 14, 28, and 72 days after compost application. The composts were applied as a 2.5 cm thick layer on the soil surface. During sampling, only the soil underlying compost was sampled. Soil pH and total organic carbon were not affected by the amendments. Soil respiration was significantly higher in compost-amended soils compared with the unamended soil except with C4 on day 72. Addition of composts increased plant growth, and P uptake being highest on day 72 with C1 and C4. With little effect on available P concentration on day 14, there was a conversion of organic P into inorganic P in the compost treatments suggesting net mineralization of organic P on day 28. On day 72, the concentrations of the less labile P forms were higher in the compost treatments compared with the unamended suggesting precipitation and fixation as well as synthesis of organic P. This study showed that mulching with composts having high available and total P concentrations can provide plants with P and also increase soil P concentrations which could reduce the fertilizer requirement for the following crop.  相似文献   
72.
APETALA1(AP1)基因既是花分生组织特征基因又是花器官形成发育基因,在花发育过程中起着关键作用。根据Genbank已知的AP1同源基因序列设计合成一对简并引物,以小黑杨(Popu-lus simonii×P.nigra)cDNA为模板,采用PCR方法分离克隆得到一个AP1同源基因全长,推测是小黑杨AP1基因,命名为XxAP1(GenBank accessionNo.XM002316040.1)。XxAP1编码249个氨基酸,开放阅读框长度747bp,蛋白质分子量28.67kD,等电点9.45。同源性分析表明,它们的核苷酸序列与其他木本植物的AP1同源基因的一致性达70%以上,推测它们具有相似功能。试验分析表明,XxAP1第1至第60个氨基酸为MADS盒结构域,说明XxAP1蛋白以序列特异方式与DNA结合,具有转录调节因子功能,第75至174个为K盒结构域,它负责蛋白质与蛋白质间的相互作用,其大多数氨基酸具有亲水性,使XxAP1蛋白具有较好的水溶性,促进蛋白的流动性有利于基因的转录。采用半定量RT-PCR技术检测XxAP1在雄花芽发育过程中的表达模式,结果显...  相似文献   
73.
氮磷钾养分配比对温室土培黄瓜产量及品质的影响   总被引:3,自引:0,他引:3  
在日光温室内,采用盆栽方式研究了不同氮磷钾养分配比对土壤栽培黄瓜产量及其品质的影响。结果表明:增加磷素用量和比例可以显著提高黄瓜的产量;适量氮钾肥配合增施磷肥可以增加果实中可溶性蛋白含量,适量氮磷肥配合增施钾肥可以改善果实品质,提高可溶性糖和维生素C含量,降低硝酸盐含量。  相似文献   
74.
长期施肥对红壤磷组分及活性酸的影响   总被引:3,自引:0,他引:3  
以12年的红壤长期肥力监测定位试验不同处理土壤为材料,研究了连续施肥对土壤磷组分、土壤对磷吸附解吸、土壤活性酸铝的影响。连续施用化学磷肥和化肥加有机肥,均可提高土壤全磷、无机磷数量。施用有机肥料,土壤中的磷以Ca-P和Al-P积累为主要表现形式,化学磷肥的施用能够提高土壤的全磷,并以Al-P增幅为最大,在所有处理中均表现为土壤O-P相对稳定。有机肥料处理土壤对外源磷的吸附强度明显少于施用化学磷肥和不施用磷肥的处理,有机肥料能够显著提高吸附磷的再利用,在NPKM处理中解吸磷占吸附磷的47.72%,M处理中占42.89%,其它处理中解吸磷占吸附磷数量一般少于8%。MNPK、M处理的PFI为2.51、2.69比N、NP处理4.53、4.37明显降低。在红壤旱地长期施用化学肥料,土壤交换性酸铝成倍增加,土壤酸化严重;施用有机肥料、有机肥料与化学肥料配合施用,土壤交换酸铝表现稳定。  相似文献   
75.
氮、磷、钾肥对丹参根系生长及养分含量的影响   总被引:1,自引:0,他引:1  
采用田间小区试验方法,研究了氮、磷、钾肥对丹参根系生长及养分含量的影响。结果表明,氮、磷、钾肥能够促进丹参根系对氮、磷、钾的吸收,提高其含量,并且随着施用量的增加而提高,在N,P2O5,K2O的施用量分别为225,180,225 kg/hm2时,根的氮、磷、钾含量达到最高值;当施入N,P2O5和K2O分别为225,120,150 kg/hm2时,丹参根干质量、根长及根条数达到最高值,根的直径最适宜,此后随着磷钾肥施入量增加,根干质量及根长、根条数反而下降,根直径增加。所以氮、磷、钾合理配合施用能够提高丹参根的养分含量、根干质量、根长、根数及根直径。  相似文献   
76.
采用室内土柱模拟试验,研究在山东平均降雨条件下不同施磷量对褐土各组分无机磷含量及形态转化的影响.结果表明,经过模拟降雨后,在0~10 cm土层中,各施磷处理的无机磷总量随着施磷量的增加而升高;随着土层的加深(10~50 cm),各土层无机磷总量是施磷量为P2(180 kg/hm2)时最高.而在10-30 cm土层,是施磷量为P3(1440 ks/hm2)的土壤无机磷总量高于P1,而在30~50 cm则是P1高于P3.同时,不同施磷量对磷组分含量及其占无机磷总量的比例都发生了改变,当施磷量分别为P1、P2和P3时,各无机磷组分的含量及所占比例按高低排序分别为:Ca10-P>Al-P,O-P>Ca8-P>Fe-P>Ca2-P;O-P>Ca8-P,Ca10-P>Fe-P,AI-P>Ca2-P和Ca10-P,O-P>Fe-P,Ca8-P>Al-P>Ca2-P.随着土层深度的加深,O-P、Fe-P和Ca10-P的含量保持相对稳定,而有效态无机磷源(Ca2-P、Ca8-P和AI-P)有降低的趋势;在小雨强度下,不同施磷量处理的土壤磷淋失量差异不显著,而随着降雨强度的加大,P3处理的土壤磷淋失量明显高于PI和P2处理的磷淋失量.以上结果说明,施磷量显著影响无机磷总量、各组分无机磷含量及其转化;在大于中等降雨条件下,高磷处理磷淋失量明显高于低磷处理磷淋失量.  相似文献   
77.
白菜S位点糖蛋白基因的克隆与表达分析   总被引:1,自引:0,他引:1  
 以白菜自交不亲和系为材料,采用RT-PCR技术,用特异引物对SLG基因进行克隆,获得SLG基因cDNA序列长度为1 324 bp,命名为BcSLG。序列分析表明:所获得的白菜BcSLG基因cDNA序列包含一完整的编码框,编码432个氨基酸,含有12个保守的半胱氨酸残基和7个N-糖基化位点。序列比对和系统进化分析表明:BcSLG与其它植物的SLG基因氨基酸序列具有较高的同源性,与大白菜和甘蓝亲缘关系最近。荧光定量PCR分析表明:BcSLG基因在自交不亲和系的柱头中表达量最高,其次是花蕾,叶片中表达最低, 在自交亲和系的柱头、花蕾和叶片中相对表达较低。  相似文献   
78.
樱桃番茄嫁接砧木筛选研究   总被引:2,自引:0,他引:2  
以格格樱桃番茄作接穗,农优野茄、托鲁巴姆、金钻砧木和砧木1号作砧木,进行嫁接和嫁接苗栽培试验.试验结果表明.4种砧木与樱桃番茄嫁接亲和性由强到弱依次为:砧木1号、金钻砧木、农优野茄和托鲁巴姆;嫁接苗青枯病发病率与自根苗差异均达到极显著水平,嫁接苗产量比自根苗增产15.9%~48.7%,在抗青枯病和产量方面表现都比较好的砧木为农优野茄和砧木1号.  相似文献   
79.
AIM To investigate the effects of cytochrome P450 (CYP450) epoxygenase/epoxyeicosatrienoic acid (EET) pathway on insulin resistance in obese mice, and to explore the possible mechanisms. METHODS High-fat diet-induced obesity model was established in C57BL/6Cnc mice, and the obese mice were randomly divided into 3 groups, including obesity group (treated with saline; n=10), EET group (treated with 11,12-EET; n=10) and EET inhibitor 14,15-epoxyeicosa-5(Z)-enoic acid (EEZE) group (n=10). Normal C57BL/6Cnc mice (n=10) treated with saline served as control. Protein expression of CYP2J2 (one of CYP450 epoxygenases) and hypoxia-inducible factor-1α (HIF-1α) was measured by Western blot. Vessel-like structure was detected by immunofluorescence staining. The serum levels of insulin, tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, IL-6 and monocyte chemoattractant protein-1 (MCP-1) were measured by ELISA. RESULTS In obese mice, homeostasis model assessment of insulin resistance (HOMA-IR) values were increased, the protein level of CYP2J2 was reduced, and the protein level of HIF-1α was increased in adipose tissues as compared with the controls (P<0.05). The serum levels of MCP-1, IL-1β, IL-6 and TNF-α were also significantly increased in obese mice (P<0.05). After treatment with 11, 12-EET, the HOMA-IR values were decreased compared with vehicle-treated obese mice, HIF-1α expression levels were decreased in the adipose tissue, and the serum levels of MCP-1, IL-1β, IL-6 and TNF-α were reduced (P<0.05). Immunohistochemical results of adipose tissue from vehicle-treated obese mice showed a marked decrease in vessel-like structures (CD31-positive) compared with normal control mice (P<0.05). EET treatment significantly increased the newly formed vessel-like structures in the visceral adipose tissues of obese mice as compared with vehicle-treated obese mice (P<0.05). CONCLUSION High-fat diet-induced obesity and insulin resistance are closely related to the CYP450 pathway. Exogenous EETs effectively decrease obesity-induced insulin resistance possibly through pro-angiogenesis and attenuation of hypoxia and inflammation.  相似文献   
80.
AIM: To investigate the effects of dexmedetomidine (DEX) on acute alcoholic hepatic injury in mice and to explore the possible mechanisms. METHODS: Kunming mice (n=50) were randomly divided into 5 groups (n=10): normal saline control (NS) group, acute alcoholic hepatic injury model (E) group, low-dose (10 μg/kg) DEX (E+L) group, medium-dose (50 μg/kg) DEX (E+M) group and high-dose (100 μg/kg) DEX (E+H) group. The animals were sacrificed at 6 h after gavage of alcohol or normal saline. The levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), triglyceride (TG), malondialdehyde (MDA), glutathione (GSH) and superoxide dismutase (SOD) were measured. The livers were removed for evaluation of histological characteristics and determining the content of tumor necrosis factor-α (TNF-α) amd interleukin-1β (IL-1β) in the liver tissues by ELISA. The expression levels of cytochrome P450 2E1 (CYP2E1) and nuclear factor-κB (NF-κB) in the liver tissues were evaluated by Western blot. RESULTS: Compared with NS group, the levels of ALT, AST and TG were obviously increased in E group, which were obviously decreased in E+M and E+H groups. Compared with NS group, the levels of TNF-α, IL-1β and MDA were obviously increase in E group, which were obviously decreased in E+M and E+H groups. Compared with NS group, the activity of SOD and the content of GSH were obviously decreased in E group, which were obviously increased in E+M and E+H groups. Compared with NS group, the expression of CYP2E1 and NF-κB was obviously increase in E group, which was obviously decreased in E+M and E+H groups. Compared with NS group, ethanol induced marked liver histological injury, which was less pronounced in E+M and E+H groups. CONCLUSION: DEX has a protective effect on mouse liver with acute alcoholic injury by the involvement in the processes of antioxidation and antiinflammation, and its mechanism may be associated with the inhibition of CYP2E1 and NF-κB expression.  相似文献   
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