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61.
本研究选用了埋植CIDR栓法、埋植PRID栓法、PG法以及PMSG+PG法四套方案对西藏41头母牦牛进行了超数排卵试验。试验结果:埋植CIDR法得到的平均卵母细胞数为7.4枚/头,埋植PRID法得到的平均卵母细胞数为6.5枚/头,PG法得到的平均卵母细胞数为4枚/头,PMSG+PG法得到的平均卵母细胞数为4.8枚/头,各组之间差异极显著(P<0.01);而经过卵母细胞成熟培养之后,埋植CIDR法得到的平均可用卵母细胞数为6.2枚/头,埋植PRID法得到的平均可用卵母细胞数也为6.2枚/头,PG法得到的平均可用卵母细胞数为4枚/头,PMSG+PG法得到的平均可用卵母细胞数为4.6枚/头,CIDR+FSH法与PRID+FSH法两组、两次PG法与PMSG+PG法两组差异不显著(P>0.05),但是CIDR+FSH法和PRID+FSH法组与两次PG法和PMSG+PG法组之间差异都极显著(P<0.01);用CIDR法和PRID法进行西藏牦牛超排效果较好,并可获得较多的可用卵母细胞。 相似文献
62.
为改善有刺黄龙果在引种地区的生长势,提高其抗逆性,本研究探讨了不同砧木和嫁接方法对有刺黄龙果嫁接育苗的影响,以期筛选到适宜有刺黄龙果的砧木和嫁接方法。结果表明,不同砧木和嫁接方法对有刺黄龙果的成活率、出芽率和新芽长势有显著影响。嫁接30天时,芽接、楔接、套接和平接法的愈合率显著高于插接和靠接法。嫁接45天时,平接、靠接和楔接法的出芽率较高,分别是76.7%、76.7%和66.7%。嫁接苗田间定植2个月时,平接、靠接和楔接法嫁接苗长势较快。其中楔接法嫁接效率高,适合工厂化批量嫁接。白肉品种‘无刺黄龙’和红肉品种‘金都1号’、‘富贵红’是有刺黄龙果嫁接的优良砧木,嫁接2个月时出芽率分别为86.7%、90.0%和86.7%,且新芽高度和宽度均大于其他砧木。综上所述,适宜有刺黄龙果规模化嫁接育苗的嫁接方法是楔接法,砧木是‘金都1号’、‘富贵红’和‘无刺黄龙’。 相似文献
63.
The objective of this study was to develop equations for estimating ileal digestible crude protein (CP) and metabolizable energy (ME) contents of meat meal (MM) and meat and bone meal (MBM) as feed ingredients for pigs based on in vitro assays. Test ingredients were 4 sources of MM and 3 sources of MBM. Ash and CP contents of the ingredients ranged from 3.8% to 33.1% and 46.8% to 82.9% (as-is basis), respectively. In vitro ileal disappearance (IVID) of CP was determined and ileal digestible CP content was calculated by multiplying CP content by IVID of CP. In vitro total tract disappearance (IVTTD) of dry matter (DM) was determined and ME was calculated using gross energy, CP contents, and IVTTD of DM. The IVID of CP and IVTTD of DM ranged from 77.2% to 88.7% and from 82.7% to 92.4%, respectively. Calculated ileal digestible CP and ME contents ranged from 37.8% to 73.5% DM and 2,405 to 3,905 kcal/kg DM, respectively. Ash contents were negatively correlated (P < 0.001) with CP (r = −0.99), in vitro ileal digestible CP (r = −0.97), gross energy (r = −1.00), in vitro digestible energy (r = −0.97), and adjusted ME (r = −0.97). The most fitting equations for ileal digestible CP and adjusted ME were: ileal digestible CP (% DM) = 11.91 − 0.90 × Ash (% DM) + 0.74 × IVID of CP (%) (R2 = 0.99) and adjusted ME (kcal/kg DM) = 130.85 − 50.90 × ash (% DM) + 47.06 × IVTTD of DM (%) (R2 = 0.99). To validate the accuracy of the prediction equations for ME, mean bias and linear bias were determined using a regression analysis. Calculated ME values of MM and MBM were in a good agreement with data obtained from animal experiments based on a statistically insignificant bias in the models. In conclusion, ME concentrations of MM and MBM as swine feed ingredients can be calculated using ash concentration and in vitro disappearance of dry matter. 相似文献
64.
建立依赖解旋酶恒温基因扩增(helicase-dependent isothermal DNA amplification,HDA)快速检测发酵乳中沙门氏菌方法。以沙门氏菌invA基因序列为目的基因,设计特异性引物,优化反应体系中UvrD解旋酶及T4 gp32添加量,建立最优反应体系。通过HDA方法直接检测发酵乳中沙门氏菌,扩增其产物后进行电泳检测,验证方法特异性。结果表明:采用HDA快速检测法检测发酵乳中沙门氏菌特异性良好,优化后反应体系体积50 μL时,UvrD解旋酶添加量为0.10 μg,T4 gp32添加量为5.0 μg,得到与设计序列长度(304 bp)一致的扩增产物,检出限为2.6×102 CFU/g;该方法用于快速检测发酵乳中沙门氏菌能够满足检测需求,具有较高的灵敏度、易操作,可作为一种基础且快速的方法检测发酵乳中沙门氏菌。 相似文献
65.
研究采用响应面法并以滤纸酶活力(filter paper activity,FPA)作为响应值对转透明颤菌血红蛋白基因的里氏木霉(Trichoderma reesei)Tu6-VHb菌株液体发酵产纤维素酶的发酵条件进行优化。根据单因素试验结果设计P-B试验,筛选出影响Tu6-VHb菌株发酵产酶的3个显著因素:吐温-80含量、发酵液体积(250 mL三角瓶发酵)、氮源浓度。用最陡爬坡路径法逼近最大响应值区域,运用响应面B-B试验设计确定3个显著因素之间的交互作用和最佳发酵条件。结果显示,Tu6-VHb产纤维素酶的最佳发酵条件是:吐温-80含量0.39%,发酵液体积61.32 mL(250 mL三角瓶发酵),氮源浓度0.87%。经优化后,Tu6-VHb菌株发酵产纤维素酶酶活力达51.72 U/mL,与模型预测值51.94 U/mL相近,较优化前该菌株酶活力(39.984 U/mL)提高了29.35%,是未转入透明颤菌血红蛋白基因的里氏木霉(Trichoderma reesei)Tu6菌株酶活力(35.904 U/mL)的1.44倍。 相似文献
66.
67.
E. Vandermeulen I. van Hoek C. De Sadeleer A. Piepsz H.R. Ham T. Bosmans A. Dobbeleir S. Daminet K. Peremans 《Journal of veterinary internal medicine / American College of Veterinary Internal Medicine》2008,22(2):266-272
Background: Chronic kidney failure is frequently seen in middle-aged and elderly cats. 51 Chromium-ethylene diaminic tetraacetic acid (51 Cr-EDTA) clearance and single blood sample (SBS) method are used in several species to estimate the glomerular filtration rate (GFR).
Hypothesis: The hypothesis of this study was that51 Cr-EDTA clearance could be determined using an SBS method in normal and hyperthyroid cats.
Animals: Forty-six cats were included in this study, with an average age of 9.5 years. Of these cats, 27 had hyperthyroidism; 19 were healthy.
Methods: After IV injection of51 Cr-EDTA (average dose: 4.25 MBq), 7 blood samples were obtained between 5 and 240 minutes. Reference clearance was calculated in mL/min and mL/min/kg body weight, using a 2-compartment model. Optimal time for clearance measurement with SBS was then determined by systematically comparing each individual plasma concentration to the reference multisample clearance.
Results: The average reference plasma clearance of51 Cr-EDTA for all cats was 14.9 mL/min (3.7 mL/min/kg). The clearance in hyperthyroid cats averaged 16.4 mL/min (4.3 mL/min/kg) and in normal cats averaged 10.3 mL/min (2.4 mL/min/kg).
The optimal time for the SBS was 48 minutes after injection of tracer51 Cr-EDTA ( R 2 = 0.9414), giving the following converting equation: clearance = (0.0066 × DV48 minutes ) – 0.9277 (in mL/min).
Conclusions and Clinical Importance: In this study, the single sample51 Cr-EDTA clearance method was used to estimate the global GFR in cats. The method identified differences in clearance between normal and hyperthyroid cats. The optimal time for an SBS was 48 minutes. 相似文献
Hypothesis: The hypothesis of this study was that
Animals: Forty-six cats were included in this study, with an average age of 9.5 years. Of these cats, 27 had hyperthyroidism; 19 were healthy.
Methods: After IV injection of
Results: The average reference plasma clearance of
The optimal time for the SBS was 48 minutes after injection of tracer
Conclusions and Clinical Importance: In this study, the single sample
68.
柞蚕微孢子虫胶体金免疫层析检测法 总被引:1,自引:0,他引:1
利用柞蚕微孢子虫孢子液直接免疫家兔获得柞蚕微孢子虫多克隆抗体后,分别采用双抗夹心法和竞争法制作胶体金免疫层析试纸条,建立能简便、快捷、准确诊断柞蚕微粒子病的柞蚕微孢子虫胶体金免疫层析检测法。双抗夹心法和竞争法分别是将柞蚕微孢子虫多克隆抗体与25 nm和17 nm的胶体金颗粒结合并固定在金标垫上,然后均将羊抗兔二抗包被在硝酸纤维素膜上作为质控点(C),但是2种方法制作的胶体金免疫层析试纸条的反应模式不同:前者是以柞蚕微孢子虫多克隆抗体作为检测点(T),而后者以柞蚕微孢子虫孢壁蛋白作为检测点(T)。2种方法制作的胶体金免疫层析试纸条的检测时间均为10 min,检测灵敏度为0.8×107个/mL,与柞蚕血淋巴无交叉反应,特异性强,操作简单,其中,以双抗夹心法制作的试纸条显色更清晰,结果更可靠,更具实用价值。 相似文献
69.
瘤胃微生物作为一个完整的生态系统,受日粮成分、饲养方式、季节等诸多因素的影响,认识瘤胃微生物的功能及其活动规律复杂而困难。瘤胃微生物的传统定量方法有亨氏滚管法和最大或然数计数法,二者有着各自的优缺点。本文综述了瘤胃微生物的传统定量方法的应用状况及各自的优缺点。 相似文献
70.