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11.
以不同栽培代数的木麻黄(第1代FCP、第2代SCP、第3代TCP)根际土壤为试验材料,运用BIOLOG微平板和磷脂脂肪酸(PLFA)技术分析根际土壤微生物群落结构和功能多样性对多代连栽响应。结果表明,不同代数的土壤微生物对各类碳源的利用程度存在显著差异,连栽后木麻黄根际土壤微生物对碳源利用率显著下降。在6类碳源中,除胺类外,其他5种碳源均呈现FCP>SCP>TCP。PLFA分析共检测到11种PLFA生物标记,FCP土壤微生物PLFA生物标记总量明显高于SCP和TCP,3个代数土壤中含量最高的PLFA生物标记是i16:0、a15:0和18:1ω9c。土壤中特征微生物含量差异明显,细菌分布量最大,其次是真菌和放线菌。随栽植代数增加,细菌含量减少,真菌含量增加。土壤微生物群落多样性指数均呈现FCP>TCP>SCP,与土壤理化性质变化密切相关。可见木麻黄连栽显著影响其根际土壤微生物群落结构与功能,因此根际土壤微生态失衡可能是导致木麻黄连栽障碍的重要因素。 相似文献
12.
采用响应面法优化超声波辅助提取薏苡仁低聚糖的工艺条件。在单因素试验基础上,选取液料比、超声波时间以及超声波功率3个因素结合Box-Behnken试验建立数学模型,分析考察3个因素对薏苡仁低聚糖响应值的影响程度,优化工艺参数。各因素对薏苡仁低聚糖提取率影响程度从大到小顺序依次为:超声波功率超声波时间液料比。响应面设计法优化出其最佳超声波提取条件为:超声波温度70℃,液料比33∶1(m L/g),超声波时间27 min,超声波功率450 W。在该条件下,薏苡仁低聚糖提取率为0.94%,与模型预测值0.98%接近。说明使用响应面法优化超声波辅助提取薏苡仁低聚糖的工艺条件是可行的。 相似文献
13.
【目的】研究不同浓度重金属铅(Pb^2+)和镉(Cd^2+)对火炬树Rhus typhina种子萌发及幼苗生长的影响,探索火炬树对重金属铅、镉胁迫的耐受程度及机理。【方法】采用培养皿滤纸发芽法,分别用不同浓度Pb^2+(300、600、900、1200、1500 mmol/L)、Cd^2+(140、280、420、560、700 mmol/L)溶液处理火炬树种子,测定种子发芽率、发芽指数、幼苗胚根长和茎长、硫代巴比妥酸(TBARS)含量、可溶性蛋白含量、超氧化物歧化酶(SOD)活性及过氧化物酶(POD)活性。【结果】与对照相比,不同浓度Pb^2+、Cd^2+均对火炬树种子的发芽率、发芽指数和幼苗生长有抑制作用,但低浓度Pb^2+可促进根长和芽长的伸长。随着Pb^2+和Cd^2+溶液浓度的增加,幼苗叶片中SOD活性和可溶性蛋白含量表现为先增加后降低,POD活性和TBARS含量均逐渐升高。其中,Cd^2+浓度为700 mmol/L时,发芽率、发芽指数、芽长和SOD活性达到最低值,而TBARS含量最高;Pb^2+浓度为1500 mmol/L时,根长达到最低值,POD活性达到最高值;Pb^2+浓度为600 mmol/L时,可溶性蛋白含量最高。【结论】Pb^2+浓度为300 mmol/L时会抑制火炬树种子萌发,但会促进幼苗生长,其余浓度Pb^2+、Cd^2+胁迫下,火炬树种子与幼苗受到一定影响,但是均较好完成了萌发与幼苗生长,并表现出多种积极的适应性特征,未出现无根苗现象,火炬树较其他木本植物对铅、镉2种重金属表现出更强的耐性。本试验结果可为今后选用火炬树作为重金属污染土壤的植物修复材料提供理论参考。 相似文献
14.
上海水稻精量机械穴直播技术研究与应用 总被引:3,自引:0,他引:3
以上海地区主推水稻品种为材料,在精量机械穴直播条件下,开展了不同类型水稻品种的小区试验和示范,明确了精量机械穴直播水稻的生育特性、抗倒伏性、群体建成和产量表现,并分析了采用水稻精量机械穴直播后土壤的微生物群落结构的变化和水稻生产经济效益。试验示范结果表明,精量机械穴直播水稻生育期明显缩短,单株分蘖力强,群体结构合理,穗粒结构协调,干物质积累多,抗倒能力较强,增产优势明显,节本低耗,生产效率显著提高,是目前极具生产潜力的一种新型高效低耗种植模式,适合上海都市农业发展的需求,也顺应了水稻低碳种植发展趋势,具有广阔的应用前景。 相似文献
15.
LIU Xing-mei ZHANG Ying-ying WANG Yuan-yuan SHI Ming-jun XIAO Ying ZHANG Fan GUO Bing 《园艺学报》2019,35(12):2169-2174
AIM: To observe the changes of Notch1 expression and autophagy in the renal tissues of diabetic mice, and to explore the regulatory effect of Notch1 on tubulointerstitial fibrosis by inhibiting autophagy in diabetic nephro-pathy. METHODS: The mice were randomly divided into normal control group (db/m mice) and diabetes group (db/db mice), with 8 rats in each group. After 12 weeks of feeding, the mice were sacrificed and the corresponding biochemical indexes were measured. The protein expression of Notch1 in the renal tubular epithelial cells was observed by immunohistochemical staining. The protein levels of Notch1, PTEN, p-Akt (Thr308), Akt, p-mTOR (Ser2448), mTOR, LC3, P62, collagen type Ⅰ (Col-Ⅰ) and collagen type Ⅲ (Col-Ⅲ) were determined by Western blot. RESULTS: Compared with the db/m mice, the blood glucose, glycosylated hemoglobin, serum creatinine, triglyceride and total cholesterol were increased in the db/db mice (P<0.01). Renal tubular epithelial cell vacuolar degeneration, renal tubular expansion and interstitial inflammatory cell infiltration in db/db mouse renal tissues with HE staining were observed. The images of Masson staining showed collagenous fiber-like substance deposition in the glomerular capillaries and renal interstitium, and disarrangement of tubular structure in the renal tissues of db/db mice. The protein expression levels of PTEN and LC3-Ⅱ were decreased (P<0.01 or P<0.05), while the protein levels of Notch1, P62, p-mTOR (Ser2448), p-Akt (Thr308), Col-I and Col-III were increased in the db/db mice as compared with the db/m mice (P<0.01). However, no significant change of total mTOR and Akt proteins between the 2 groups was found. CONCLUSION: Notch1 protein expression was increased, PTEN expression was significantly reduced, Akt/mTOR pathway was activated, autophagy was inhibited, and fibrosis was aggravated in the renal tissues of the diabetic mice. 相似文献
16.
17.
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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19.
[目的]建立文心兰高效再生体系,为利用转基因技术进行品种改良提供科学依据.[方法]以文心兰柠檬绿的无菌苗叶片为材料,探讨不同植物生长调节剂配比对其原球茎诱导的影响,开展增殖、生根及移栽研究,建立其高效稳定的再生体系.[结果]影响文心兰原球茎诱导的3种植物生长调节剂主次排序为萘乙酸(NAA)>噻苯隆(TDZ)>6-苄氨基嘌呤(6-BA),在1/2MS培养基中添加0.5 mg/L NAA、0.5 mg/L 6-BA和0.3 mg/L TDZ的诱导率最高,达48.0%.培养基中活性炭含量及碳水化合物种类对文心兰原球茎增殖的影响存在明显差异,不同活性炭含量处理间的原球茎增殖系数存在显著差异(P<0.05,下同),添加1.0 g/L活性炭较添加0.5 g/L活性炭的增殖系数显著升高,不同碳水化合物种类间的原球茎增殖系数排序为海藻糖>麦芽糖>蔗糖,最佳增殖和分化培养基为1/2MS+4.0 mg/L 6-BA+0.4 mg/L NAA+1.0 g/L活性炭+20 g/L海藻糖.添加10%椰子水的文心兰幼苗生根数显著高于添加10%香蕉汁和10%苹果汁,每株平均生根量接近4.00条,即生根效果最佳的培养基为1/2MS+0.8 mg/L 6-BA+0.2 mg/L NAA+10%椰子水.移栽过程中根部用水苔包裹后再移至椰糠中,保证光照、水分适宜,适当添加缓释肥,移栽成活率可达100%.[结论]利用海藻糖或麦芽糖作为碳源的文心兰原球茎增殖效果较优,生根数和生根质量优势明显;不同植物生长调节剂配比、碳源和有机物的添加对文心兰组织培养具有明显的促进效果. 相似文献
20.
AIM: To investigate the role of zerumbone (ZER) in 1-methyl-4-phenylpyridinium (MPP+)-induced cytotoxicity of human neuroblastoma SH-SY5Y cells. METHODS: Human neuroblastoma SH-SY5Y cells were cultured in vitro and the protective effect of ZER against MPP+-induced cytotoxicity was measured by CCK-8 assay. Flow cytometry was used to determine the apoptosis and reactive oxygen species (ROS). The expression of Parkinson disease protein 7 (PARK7) was knocked-down by using PARK7-specific short hairpin RNA (shRNA). The protein levels of PARK7, nuclear factor E2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) were determined by Western blot. RESULTS: MMP+ remarkably reduced the cell viability in a dose-dependent and time-dependent manner. The SH-SY5Y cell injury model was established by treatment with MPP+ at 600 μmol/L for 24 h. ZER up-regulated the protein levels of PARK7 and Nrf2 (P<0.05), alleviated apoptosis (P<0.05), and reduced ROS production (P<0.05) in the SH-SY5Y cell injury model. Meanwhile, N-acetyl-L-cysteine (NAC) had the similar functions. Moreover, significant reductions in the protein levels of Nrf2 and HO-1 (P<0.05), and obvious increases in apoptosis (P<0.05) and ROS level (P<0.05) were demonstrated in PARK7-knockdown cells. CONCLUSION: ZER protects SH-SY5Y cells against MPP+-induced cytotoxi-city, which may be related to activation of PARK7/Nrf2/HO-1 pathway, and subsequent attenuation of oxidative stress and apoptosis. 相似文献