马尾松截根苗造林林分生长状况分析

由于马尾松常规苗主根发达，侧根较少，造林成活率较低。1990年起选用了马尾松截根苗造林，以期提高其造林成活率，取得了较好的效果。^[1-2]通过对马尾松截根苗造林13年生林分生长现状调查分析，试图进一步揭示截根对林木生长的影响，为大力推广应用截根苗造林提供了科学的理论依据。     

大白菜新品种中熟6号的选育

中熟 6号是由大白菜雄性不育系 98- 2 - 1和从丰抗 70中多代自交分离而选育出的自交系F - 3-2 - 3配制而成的优良一代杂种。抗霜霉病、病毒病与软腐病 ,生长期 6 0～ 6 5d(天 ) ,叶球叠抱、圆头、卵圆形。南方栽培平均单球质量 2 .0kg ,每 6 6 7m2 产量 4 0 0 0～ 5 0 0 0kg。     

小麦条锈病流行程度趋势预测专家系统雏型

本文运用知识工程语言 M·1构造了一个用于小麦条锈病流行程度趋势预测的专家系统雏型。专家的知识用产生式规则来表示。知识库中的知识规则可相对独立,便于知识库的扩充和完善。     

植物活体水分探测仪的研制及测试初报

利用NIM插件探测器及金硅面垒探头组装了植物活体水分探测仪;筛选并分析了仪器的最佳工作条件;检测了春小麦、玉米、苜蓿、豌豆、红豆草叶片鲜重的变化。结果表明;叶片水分随时间损失大的,其抗旱性差。叶片保水的秩序为:红豆草、豌豆>苜蓿>春小麦>玉米。     

云南省世界银行贷款“国家造林项目（NAP）”科技推广

本文报告了云南世行贷款“国家造林项目（ＮＡＰ）”的科技推广后所取得的成效。为了增加项目造林的科技含量，项目一启动就重视科技成果的推广，前后推广了省内外重要科技成果６项，对主要造林树种建立了试验林、示范林、环境保护监测样地，以及配套的科学管理等措施。通过这些举措，使项目造林取得显著成效，完成造林任务６４２７５．８１ｈｍ２（９６．４万亩），为协议任务面积的１４６．１％，造林成活率达９５％以上，保存率达９０％以上。由于生产与科技紧密结合，从而大大提高了科学造林水平，使“ＮＡＰ”项目在省内工程造林中起到了示范作用。     

猪胚胎干细胞的分离克隆

本文从分化抑制物、培养基的选择内细胞团的分离,胚胎干细胞的分离及鉴定方法等方面系统地综述了猪胚胎干细胞分离克隆的研究进展;并对其未来的应用前景进行展望。     

稀释液渗透压对绵羊精液冷冻效果的影响

本试验对绵羊冻精采用两次稀释时,从调整Ⅱ液中葡萄糖含量和降低甘油浓度两方面,改变稀释液的渗透压,测定冻精效果。先增减糖的比例,配制9-2(对照), 84-1和84-2等试验组,其稀释Ⅱ液渗透压1191,1026、1499mmol/kg,获冻精情期产羔母羊率61.69, 63.31, 54.55(P<0.05)。随后, 以84-1为对照,降低甘油浓度,设3个试验组,即87-2,88-1和88-1a,渗透压相应为747,456,463mmol/kg,冻精情期受胎率1987年84-1,87-2为65.37,67.37;1988年87-2,88-1,88-1a为63.16,62.50,46.55(P<0.05)。试验说明,绵羊冻精采取2次稀释法,第Ⅱ液以4％甘油,渗透压为747mmol/kg时,冻精效果最佳。     

鸣禽鸟的发声中枢及其神经传导通路的研究

鸣禽鸟的发声中枢及其神经传导通路的研究曾庆华，赵玲，姜立嘉（东北师范大学生物系）鸣禽鸟之所以能发出婉动听的鸣叫，不仅仅是依赖于外围发声器（鸣管）来完成，而是经过多级水平的相关中枢组成的机能系统密切配合统一调节方能完成的。这个机能系统称它为各级发声中枢...     

包心菜无菌苗子叶及叶片原生质体高频分裂和高频植株再生

以包心菜子叶和叶片原生质体为材料。经不同液体培养基(Bp1,Bp2,B1)浅层培养,再生细胞高频分裂并形成愈伤组织。愈伤组织经扩增后转移到分化培养基上诱导植株分化,从这两种原生质体中获得了再生植株。在原生质体培养过程中,原生质体及细胞团的褐化程度与培养基中的有机成分的多少有关。原生质体的分化频率与培养基中植物激素种类关系甚大。在植株分化时,谷氨酰胺和腺嘌呤对植株分化有很大促进作用。另外,原生质体的来源及原生质体培养基对原生质体植株分化能力均有不同的影响。     

‘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.