配料混合试验的设计和分析

系统地介绍了配料混合试验的基本概念．指出了混合试验与常规因子试验的区别。提出配料混合试验的3种设计，即顶点和边界点设计、矩心设计和极顶设计。以2个实例演示了混合试验资料的统计方法，包括回归和方差分析．驻点分析和等值线分析。     

肾俞穴,后三里穴与子宫相关的神经基础

应用辣根过氧化物酶（ＨＲＰ）法和荧光素双标记法，研究了家兔子宫与肾俞穴、后三里穴的外周神经联系。结果显示，支配子宫与肾俞穴、后三里穴的初级传入神经元及交感节后神经元分布节段部分重叠，在腰１（Ｌ１）脊神经节有少量的荧光素双标记细胞，约占该节荧光素标记细胞总数的２．６％，表明Ｌ１脊神经节有一些初级传入神经元，其周围突分支分布于肾俞穴和子宫，提示子宫与肾俞穴除通过中枢途径联系外，还可通过外周突分支投射的感觉神经元直接相联系；在胸１２～荐３（Ｔ１２～Ｓ３）交感神经节出现大量分别支配子宫和后三里穴的标记细胞，这两种细胞紧密相邻，提示支配子宫和后三里穴的交感节后神经元之间，可能还存在直接或间接联系。上述结果为穴位－内脏相关机理提供了形态学证据。     

莫能菌素浓度对混合瘤胃微生物体外发酵的影响

本试验研究了莫能菌素对混合瘤胃微生物体外发酵的影响 ,以期确定莫能菌素在瘤胃内容物中的适宜添加浓度。混合瘤胃微生物由饲喂花生秧基础日粮的阉公牛瘤胃内容物和瘤胃液制备 ,用简易人工瘤胃装置测定莫能菌素浓度对产气量、瘤胃乙丙酸比例、粗纤维降解率和真蛋白产量的影响。结果表明 ,莫能菌素浓度强烈地抑制产气量 ,两者呈线性负相关(P<0.05);粗纤维降解率开始时随莫能菌素浓度的升高而增加 ,在浓度为0.078mg/L时达到最大值 ,两者呈二次幂函数关系 ;添加莫能菌素降低了瘤胃乙丙酸比例 ,但瘤胃乙丙酸比例随莫能菌素浓度的提高有逐渐增加的趋势 ;在莫能菌素浓度为0.1～2.0mg/L的范围内 ,添加莫能菌素对蛋白质的产量没有明显影响     

近冰点温度贮藏草莓的研究

草莓呼吸旺盛,果皮薄易受伤,难以贮藏。利用近冰点温度贮藏可以明显地抑制草莓的呼吸作用,结合小袋包装的气密性,改善了包装内部的气体组成,提高草莓果实周围的相对湿度并减少空气对流,从而抑制了草莓在贮藏过程中糖分、水分的损耗,减少了糖酸比值的下降。保持了一定的感观指标,可使草莓的贮藏时间延长。     

微生物谷氨酰胺转胺酶(MTG)分批发酵模型的建立

在本文中，以本实验优化好的工艺条件，建立了关于微生物谷氨酰胺转胺酶分批发酵的数学模型方程细胞生长的动力学方程、产物合成的动力学方程和底物消耗的动力学方程。并对所建立的动力学方程进行了生物统计分析，结果表明所建立的模型具有一定的可信度。     

中国野生种毛葡萄光合特性的研究

毛葡萄（ＶｉｔｉｓｑｕｉｎｑｕａｎｇｕｌａｒｉｓＲｅｈｄ）的净光合速率日变化值明显高于山葡萄、宝石、白玉霓，且无栽培品种光合作用的“午休”现象。毛葡萄的净光合速率与其它野生种葡萄和栽培品种比较也表现出较高水平。在进行ＣＯ２饱和点和补偿点测定时，毛葡萄也较栽培品种白玉霓有较强的光合作用，因此，毛葡萄是葡萄高光合效率育种的优良野生种质资源。     

内蒙古大兴安岭林区野生动物资源开发对策

内蒙古大兴安岭林区野生动物资源十分丰富,在积极保护的基础上,合理开发利用野生动物资源对林区培育新的经济增长点、提供就业机会具有重要意义.本文主要从药用野生动物、毛皮动物、食用动物及野生动物生态旅游产品等几个方面的开发对策进行了探讨.     

Effect of ruminal dosing of mechanical stimulating brush on rumination time, ruminal passage rate and rumen fermentation status in Holstein steers fed a concentrate diet

This experiment was conducted to determine the effect of ruminal dosing of a mechanical stimulating brush on rumination time, ruminal passage rate and rumen fermentation status in steers fed a concentrate diet at maintenance level. Animals were dosed three Rumen Faibu (RF) per head through the rumen fistulae (RF treatment) and not dosed (control) in a change‐over design. The organic cell wall content of the concentrate diet was 12.7% of dry matter. Daily time spent on rumination was very short in both treatments with 24 min in RF treatment and 15 min in control. The turnover rate of ruminal fluid in RF treatment was higher than that in control. There were no differences in ruminal pH and total volatile fatty acid concentration between RF treatment and control. Acetic and butyric acid concentrations were not different between the treatments. Propionic acid concentration tended to be higher in the animals on RF treatment than in control animals. The RF dosing in Holstein steers fed a low fiber diet did not affect the rumination time, but increased rumen digesta passage rate and ruminal propionic acid production.     

冻融中土壤的水热动态

根据在北京郊区的试验,认为土壤水冻融过程可分为三阶段,其中第二阶段有聚墒现象,平均聚墒8.6mm,所聚的墒在融化过程中又逐渐消失。气温回升至-2℃左右是冻层下部由冻到融的转折温度。冬灌水保存到来年春季的数量有限,本试验中1m 土层内平均不足20mm。     

Development of a semi-selective medium and an immunofluorescence colony-staining procedure for the detection of Clavibacter michiganensis subsp. sepedonicus in cattle manure slurry

Various compounds and basal media were tested for their suitability to create a semi-selective medium for isolation ofClavibacter michiganensis subsp.sepedonicus (Cms) from cattle manure slurry containing c. 10⁸ colony forming units (cfu) per ml.Plating efficiency of Cms in yeast glucose mineral medium (YGM) was 104% compared with yeast peptone glucose medium. Nalidixic acid, polymyxin B sulphate and the experimental disinfectant S-0208 inhibited colony growth of cattle slurry bacteria as compared with Cms in YGM. The optimal concentration of these inhibitors in combination was determined by modified agar diffusion tests and by pour plating in 24-well tissue culture plates. The semi-selective medium YGMI consisted of YGM supplemented with nalidixic acid (2 mg/l), polymyxin B sulphate (30 mg/l) and S-0208 (125 mg/l). Plating efficiency varied for Cms between 50.9 and 69.6%, for cattle slurry bacteria between 1.8 and 2.5% and for saprophytes from potato heel end extracts between 11.5 and 27.4%.Differentiation of Cms colonies from other colonies was based on their small and bluish colony morphology in pour plates and on immunofluorescence colony-staining (IFC). IFC of a pure culture of micro colonies of Cms in YGM was possible after one day incubation (colonies c. 5 cells). Green background fluorescence in the agar gels was prevented by addition of Tween 20 (0.1%) to the washing buffer and the use of 1% agar gels. IFC of macro colonies of Cms in YGMI, visible with 4x objective magnification, was possible after 4 days. The detection level of the target organism in artificially inoculated cattle slurry in YGMI based on colony morphology varied between 1.4×10³ and 2.3×10⁴ cfu per ml of cattle slurry. Miniaturized plating combined with IFC, using wells in tissue culture plates (=16 mm), proved suitable for detection, but was c. 30 times les sensitive. The recovery of Cms was negatively correlated with the number of saprophytic colonies in the agar plates (R ²=0.74).