川北地区稻田养殖中华绒螯蟹试验初探

本试验在四川山间湿地利用农田0.62公顷养殖中华绒螯蟹，放养苗种为1272只(135只／667m^2)，个体均重7g／只左右，经160d饲养，捕获绒螯蟹875只，个体均重136．7g／只，回捕率为68.8％，饵料系数为2．45，同时水稻产量3529．7kg(375．5kg／667m^2)，其总收获利润为416元／667m^2。     

沙土区薄壁连拱护岸墙试验与应用

沙土区薄壁连拱护岸墙为悬臂式支撑、薄壁连拱无底板结构，拱板中间采用无砂砼排水孔的钢筋砼肋形预制板，冲沉法施工，造价低廉；外形美观，抗倾、抗滑性能强。该墙为平原沙土区河道水土保持及修复找到了一条经济合理、施工方便、简便易行的护坡办法，具有较高的实用价值和广阔的推广使用前景。     

论中国引进判例机制的理论基础

成文法有其局限性 ,这种局限性是其本身固有而又是它自身无法克服的。判例制度正是克服了这一局限性的有效形式。     

胆盐和游离脂肪酸影响离体小肠细胞类胡萝卜素吸收的研究

用黄鸡小肠细胞进行了 β-胡萝卜素和黄体素的体外吸收试验 ,研究类胡萝卜素浓度、胆盐和游离脂肪酸对这两种类胡萝卜素吸收的影响。结果发现 :β-胡萝卜素和黄体素的吸收均呈浓度依赖性 ;牛磺胆酸钠极显著促进黄鸡离体小肠细胞类胡萝卜素的吸收(P<0.01) ,其促进 β-胡萝卜素和黄体素吸收的最佳浓度分别为3mM和10mM ;游离脂肪酸极显著促进了类胡萝卜素的吸收(P<0.01) ,其中油酸对类胡萝卜素的促吸收作用大于硬脂酸 ,促进 β-胡萝卜素和黄体素吸收的最佳油酸/硬脂酸比率分别为100 :0和3 :1。牛磺胆酸钠和游离脂肪酸影响 β-胡萝卜素吸收的动态变化模式与它们对黄体素的显著不同     

氨基酸铁在大鼠小肠中的吸收及组织中沉积研究

本试验用50日龄Wistar纯系雄性大鼠,采用体内原位结扎肠段灌注技术和放射性同位素示踪技术,研究了氯基酸螯合铁(以赖氨酸螯合铁和甘氨酸螯合铁为代表)的吸收特点。试验中观察了向结扎肠段灌注含不同形态铁的吸收液后,不同时间点(5、15、30、60、90、120分钟)血液中59Fe比放射性的动态变化;120分钟(试验结束)时不同组织器官中59Fe的放射性大小和总铁含量以及主要血液学指标的变化。试验结果表明:①赖氨酸和甘氨酸都能促进大鼠对铁的吸收。②与相应摩尔浓度的氨基酸与氯化亚铁的混合物相比,赖氨酸螯合铁和甘氨酸螯合铁能更有效地被大鼠吸收。综合分析本试验结果认为,氨基酸螯合铁都是一种优秀的铁添加剂。从本试验结果看,放射性同位素示踪技术结合结扎十二指肠段灌注技术不失为一种研究动物对微量元素吸收情况的理想试验手段。     

红豆草茬地放牧结合补饲青干草对草地羔羊育肥效果的研究

1986～1987年期间在甘肃农大牧草站进行了以红豆草茬地放牧结合补饲青干草对草地羔羊育肥效果的试验。比较了在放牧基础上3种补饲处理(即单燕麦草、单红豆草和燕麦+红豆草混合干草)对两种类型羔羊(即甘肃高山细毛羊和边甘杂种一代羔羊)增重和肉用性能的影响。试验结果表明,7月龄边甘杂种羔羊或9月龄甘高羔羊的期末活重均已超过35公斤,胴体重超过17公斤,屠宰率为47％～49％。     

小鹅瘟PCR诊断方法的建立和初步应用

根据发表的鹅细小病毒B株VP3基因序列 ,设计合成了 1对寡聚核苷酸引物。以国内分离的小鹅瘟病毒为摸板 ,筛选了 (PCR)最佳反应条件 ,并进行了敏感性、特异性和初步应用试验。结果表明 ,在 4 0 μL体积中 ,PCR最佳系统组成为 2uTaq酶、0 5mol/LdNTP和 2 0 pmol引物 ;最佳反应参数为 96℃变性 4 0s ,5 4℃退火 1min ,72℃延伸 1min ,30个循环。本方法可检出 2 5× 10 -1 5EID50 小鹅瘟病毒 ,并且仅能从小鹅瘟病毒的鹅胚培养物中扩增出与设计值大小相同的 375bp核苷酸片断 ,对照病毒扩增结果为阴性。通过对 6份临床病料的检查 ,2份呈阳性 ,其中 1份来自有典型小鹅瘟症状的雏鹅 ,1份来自无典型小鹅瘟症状的雏鹅。由此说明 ,本试验所建立的诊断小鹅瘟的PCR方法具有潜在的临床应用价值     

基于ASP.NET的造林专家系统

基于ASP NET的设计思想和实现方法,采用知识库和专家系统原理构建造林专家系统。利用该系统辅助解决造林体系中的非结构化问题,为其规划设计的论证决策提供有力工具及手段。     

‘Plantibodies’: a flexible approach to design resistance against pathogens

Engineering resistance against various diseases and pests is hampered by the lack of suitable genes. To overcome this problem we started a research program aimed at obtaining resistance by transfecting plants with genes encoding monoclonal antibodies against pathogen specific proteins. The idea is that monoclonal antibodies will inhibit the biological activity of molecules that are essential for the pathogenesis. Potato cyst nematodes are chosen as a model and it is thought that monoclonal antibodies are able to block the function of the saliva proteins of this parasite. These proteins are, among others, responsible for the induction of multinucleate transfer cells upon which the nematode feeds. It is well documented that the ability of antibodies to bind molecules is sufficient to inactivate the function of an antigen and in view of the potential of animals to synthesize antibodies to almost any molecular structure, this strategy should be feasible for a wide range of diseases and pests.Antibodies have several desirable features with regard to protein engineering. The antibody (IgG) is a Y-shaped molecule, in which the domains forming the tips of the arms bind to antigen and those forming the stem are responsible for triggering effector functions (Fc fragments) that eliminate the antigen from the animal. Domains carrying the antigen-binding loops (Fv and Fab fragments) can be used separately from the Fc fragments without loss of affinity. The antigen-binding domains can also be endowed with new properties by fusing them to toxins or enzymes. Antibody engineering is also facilitated by the Polymerase Chain Reaction (PCR). A systematic comparison of the nucleotide sequence of more than 100 antibodies revealed that not only the 3′-ends, but also the 5′-ends of the antibody genes are relatively conserved. We were able to design a small set of primers with restriction sites for forced cloning, which allowed the amplification of genes encoding antibodies specific for the saliva proteins ofGlobodera rostochiensis. Complete heavy and light chain genes as well as single chain Fv fragments (scFv), in which the variable parts of the light (V_L) and heavy chain (V_H) are linked by a peptide, will be transferred to potato plants. A major challenge will be to establish a correct expression of the antibody genes with regard to three dimensional folding, assembly and intracellular location.     

Effects of Latent Infection of Stock Plants and Abundance of Thrips on the Occurrence of <Emphasis Type="Italic">Tomato spotted wilt virus </Emphasis>in Chrysanthemum Fields

DAS-ELISA proved to be reliable enough to detect a latent infection by Tomato spotted wilt virus (TSWV) in asymptomatic stock plants of chrysanthemum. A high density of Frankliniella occidentalis, the predominant vector, in the presence of latently infected stock plants resulted in a high incidence of disease in the chrysanthemum production field. The incidence of disease was low when the vector thrips were not abundant in spite of the presence of latently infected stock plants. These results suggest that an infestation of the vector thrips causes severe secondary spread of TSWV originating from latently infected stock plants in chrysanthemum production fields. Received 27 July 2001/ Accepted in revised form 27 November 2001