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71.
72.
Growth and energy budget of juvenile cobia (initial body weight ∼ 22 g) at various temperatures (23, 27, 31 and 35 °C) were investigated in this study. Maximal ration level (RLmax, %/day) increased as temperature (T, °C) increased from 23 °C to 31 °C but decreased at 35 °C, described as a quadratic equation: RLmax = −0.023T2 + 1.495T − 17.52. Faecal production (f, mg g− 1 day− 1) increased with increased temperature (T, °C), described as a power function: lnf = 0.738lnT − 0.806. As temperature increased, feed absorption efficiency in dry weight (FAEd, %), protein (FAEp, %) and energy (FAEe, %) all increased first and then decreased, but the variation of feed absorption efficiency was small, with ranges of 89.59-91.08%, 92.91-94.71%, 93.92-95.32%, respectively. Specific growth rate in wet weight (SGRw, %/day), dry weight (SGRd, %/day), protein (SGRp, %/day) and energy (SGRe, %/day) showed a domed curve relative to temperature (T, °C), described as quadratic equations: SGRw = − 0.068T2 + 3.878T − 50.53, SGRd = − 0.079T2 + 4.536T −59.64, SGRp = − 0.084T2 + 4.783T − 63.08 and SGRe = − 0.082T2 + 4.654T − 60.99, and SGRw, SGRd, SGRp and SGRe maximized at 28.5 °C, 28.6 °C, 28.4 °C, 28.5 °C, respectively, as calculated from the regression equations. The relationships between feed conversion efficiency in wet weight (FCEw, %), dry weight (FCEd, %), protein (FCEp, %), energy (FCEe, %) and temperature (T, °C) also took on a domed curve described as quadratic equations: FCEw = − 0.726T2 + 39.71T − 473.8, FCEd = − 0.276T2 + 15.31T − 190.6, FCEp = − 0.397T2 + 22.05T − 277.9 and FCEe = − 0.350T2 + 19.39T − 239.9, and FCEw, FCEd, FCEp and FCEe maximized at 27.4 °C, 27.8 °C, 27.7 °C and 27.7 °C, respectively, as calculated from the regression equations. Energy budget of juvenile cobia fed satiation was 100C = 5F + 67(U + R) + 28G at water temperature 27 °C and 100C = 5F + 70(U + R) + 25G at water temperature 31 °C, where C is food energy, F is faeces energy, (U + R) is excretion energy and metabolism energy, and G is growth energy. 相似文献
73.
W. Aufhammer W. Wägner H.-P. Kaul E. Kübler 《Journal of Agronomy and Crop Science》2000,184(4):277-286
Radiation use by oil seed crops — a comparison of winter rape, linseed and sunflower For the production of grain crops rich in oil, winter rape, linseed and sunflower are similarly suitable at many arable locations. We wanted to compare the extent to which radiation (PAR) is intercepted and utilized by the individual species for dry matter and yield production. For this purpose, a 2‐year field experiment comprising the factors genotype, N fertilization and soil tillage was conducted. For five phases of crop development, growth rates (CGR, RGR and NAR) and PAR utilization were calculated. At full ripeness, total dry matter, grain, oil and energy yields, the crop‐ and year‐specific PAR supply, its interception and utilization for dry matter production and the resulting energy binding were determined. Due to the different individual vegetation periods, the PAR supply of the crops differed. The crop assimilation areas also differed, with values for winter rape and sunflower higher than those for linseed. The yield productivity of winter rape and sunflower was also higher than that of linseed. N fertilization increased yield to different extents for the different crops. On average, winter rape and sunflower produced the same amounts of dry matter and energy yield. Due to a higher harvest index, sunflower had the highest grain yield, and because the oil concentration in grain was comparatively high sunflower produced the highest oil yield, too. Under cool and wet climate conditions, however, the productivity of sunflower is offset by a relatively high yield risk because of uncertain ripening. The highest PAR utilization by linseed did not compensate for its very short vegetation period in combination with the lowest PAR interception. 相似文献
74.
75.
Seedling crops of gazania, geranium, marigold, mimulus, pansy, verbena and vinca were grown to 60% anthesis in three greenhouse temperature regimes: (a) 26 °C day/6 ± 3 °C night (LT), with a 16.5 °C mean daily temperature (MDT), (b) 26 °C day/17 ± 4 °C night, with a 21 °C MDT, and (c) variable day/night temperatures in response to heating and cooling by a phase change material energy storage module (PCM) with an 8 ± 2 °C night and a 16 °C MDT. Crops bloomed from 2 to 17 days earlier in the 26 °C/17 °C greenhouse. The morphological characteristics of all cultivars of gazania, mimulus, pansy and verbena, geranium and vinca were similar regardless of greenhouse temperature regime. Marigold diploid and triploid cultivars and mimulus were morphologically more variable than the other bedding plant species. Crops grown in the PCM and LT greenhouses had virtually identical morphological characteristics and bloomed in about the same number of days. Plant height was not affected by DIF environments in the greenhouses. The PCM and LT greenhouses had a similar MDT, but the distribution of numbers of hours of mean daily temperatures was different. 相似文献
76.
小尾寒羊泌乳期母羊能量需要量及代谢规律研究 总被引:4,自引:0,他引:4
选择有代表性的小尾寒羊泌乳母羊6只,分成哺育单羔和双羔两组,每组3只,分泌乳前期(1~30天),泌乳中期(31~60天)和泌乳后期(61~90天)3个阶段进行饲养试验、消化代谢试验、呼吸测热试验及屠宰试验等研究。两组试羊均按NRC(1978)推荐的绵羊泌乳期哺育双羔母羊能量需要量供给代谢能和其它养分。结果表明,在本研究条件下,小尾寒羊泌乳母羊(包括哺育单、双羔者)在整个泌乳期内的平均日干物质(DM)、有机物质(OM)、代谢能(ME)和泌乳量分别为1689g,1571g,19.893MJ和653g。DM、OM和总能(GE)表观消化率分别为70.71%,72.58%和70.34%,代谢率(MEI/DEI)为84.89%。甲烷能占GEI的9.18%。每日畜体产热量(HP)为625.5KJ/kgW0.75。研究还表明:小尾寒羊泌乳母羊的每日维持代谢能和净能需要量分别为582.6和460KJ/kgW0.75,每户1kg原乳需要10802KJ的代谢能。维持效率为0.790泌乳效率为0.479,HI占GEI的18.10%。分析结果证明,试羊的泌乳量、采食量、畜体产热量和能量转化效率在单、双羔之间均无显著差异(P>0.05)。小尾寒羊泌乳母羊的代谢能总需要量(MER)可用下式估计:羊羔:MER=576.9W0.75+10810M;双羔:MER=588.2W0.75+10794M;平均:MER=582.6W0.75+1 相似文献
77.
78.
肉用仔鸡主要营养、环境因素产量函数模型的研究 总被引:2,自引:1,他引:1
利用二次回归通用旋转组合设计对500只印第安河肉鸡生产的主要营养、环境因素进行了研究,建立了肉鸡生产函数模型,探讨了印第安河肉鸡日粮中粗蛋白质、代谢能水平及饲养密度等主要营养、环境因素及其相互效应和增重的关系,寻求了肉鸡增重最佳饲养管理措施组合方案和最优化的生产条件,为我国肉鸡生产技术的规范化提供了科学依据。肉鸡生产函数模型。y=2105.57+101.35X_1+42.93X_2-16.68X_3-16.3X_1X_2-99.47X_1~2-54.91X_2~2-51.16X_3~2。各因素对产量贡献大小顺序为粗蛋白质>代谢能>饲养密度。预测56日龄增重达1900克和净收入高于2.20元/只以上时,前期日粮需粗蛋白质21.55~22.37%,代谢能12.199~12.597MJ/kg,饲养密度32.9~34.4只/m~2;后期依次为19.55~19.76%,12.46~12.85MJ/kg,16.7~17.9只/m~2。蛋白质和代谢能存在交互作用。 相似文献
79.
AIM: To investigate the changes of peroxisome proliferator-activated receptors (PPAR)α/peroxisome proliferator activated receptor coactivator 1 alpha (PGC-1α) in doxorubicin (DOX) induced dilated cardiomyopathy (DCM) and its effect on the energy metabolism and myocardial function in mice. METHODS: Forty mice were randomly divided into 4 groups: control group, DOX group, PPARα inhibitor group and PPARα agonist group. The DCM model was established by injection of DOX. The protein levels of PPARα/PGC-1α were detected. The PPARα inhibitor and PPARα agonist were used 2 weeks beforeinjection of DOX. The contents of adenine acid and phosphocreatine (Pcr) in the mitochondria were measured by high-performance liquid chromatography (HPLC). The ANT activity was analyzed by the atractyloside-inhibitor stop technique. The changes of the echocardiography and hemodynamics were also observed. RESULTS: DOX induced DCM model was successfully established. The protein levels of PPARα and PGC-1α in control group were significantly higher than those in DOX group (P<0.05). Both of the high-energy phosphate contents and the transport activity of ANT were decreased in DOX group (P<0.05), and the hemodynamic parameters were disordered (P<0.01). Compared with DOX group, PPARα inhibitor pre-treatment significantly reduced the PPARα/PGC-1α expression. Meanwhile, high-energy phosphate contents in the mitochondria and the ANT transport activity of the mitochondria decreased, as well as the left ventricular function (P<0.05). On the other hand, PPARα agonist significantly increased the expression of PPARα and PGC-1α, and improved the transport activity of ANT. In addition, the hemodynamic parameters were ameliorated, but the high-energy phosphate contents of the mitochondria did not significantly change. CONCLUSION: PPARα/PGC-1α plays an important role in the regulation of ANT transport activity in dilated cardiomyopathy induced by DOX, and the activation of PPARα/PGC-1α has protective effects on the DCM induced by DOX. 相似文献
80.