江西省 2001年审（认）定水稻新品种

１.金优９７４由湖南省衡阳市农业科学研究所育成、江西省种子管理站引进。全生育期１１４天。株高８１ｃｍ ,结实率７５ % ,千粒重２５ｇ。对稻瘟病抗性一般。大田一般单产４２０ｋｇ／６６７ｍ２。适宜赣中、赣北地区种植。２.国丰一号由中国水稻研究所育成、江西省种子管理站引进。全生育期１２３天。株高９９ｃｍ ,分蘖力中等 ,结实率７８．８ % ,千粒重２７．５ｇ。稻瘟病抗性 :苗瘟０级 ,穗颈瘟３级。１９９８～１９９９年参加江西省水稻区试 ,１９９８年平均单产４５４．９２ｋｇ／６６７ｍ２,与对照汕优晚３平产 ;１９９９年平均单…     

无线局域网结构与应用前景

从局域网的体系结构出发 ,阐述了无线局域网 (WLAN)的传输技术、发展现状、IEEE80 2 1 1、无线局域网技术标准、无线局域网的组网方式及无线局域网的应用前景     

马立克氏病毒单克隆抗体杂交瘤细胞株的建立与鉴定

以马立克氏病毒814株(MDV-814)作为免疫用抗原,建立了2个MDV特异性单克隆抗体(McAb)杂交瘤细胞株—4A6、3D7。鉴定结果表明;两株细胞所分泌的McAb均为IgM类免疫球蛋白,具有MDVⅠ型病毒特异性,无中和反应特性和沉淀反应特性。利用两种McAb对国内标准强毒MDV-京1株进行鉴定,肯定其为MDV-Ⅰ型毒株。     

白跗平腹小蜂对主要森林害虫抑制力研究

１９８７～１９９２年连续６年研究结果表明，白跗平腹小蜂Ａｎａｓｔａｔｕｓａｌｂｉｔａｒｓｉｓ对马尾松毛虫Ｄｅｎｄｒｏｌｉｍｕｓｐｕｎｃｔａｔｕｓ、柳杉毛虫Ｄｅｎｄｒｏｌｉｍｕｓｌａｔｉｐｅｎｎｉｓ、水青蛾Ａｃｔｉａｓｓｅｔｅｎｅｎｉｎｇｐｏａｎａ等１３种主要森林害虫卵有较明显的抑制作用。在林间，该蜂对马尾松毛虫第１、２代卵的自然抑制力分别力１６．５５％和２２．２９％，对柳杉毛虫越冬代卵的自然抑制力为２３．４５％；对水青蛾第１、２代卵的抑制力分别力５．４９％和２．６３％；在林间，人为释放白跗平腹小蜂对第１代马尾松毛虫卵的校正抑制力为３３．５％，在室内１２．３～２８℃范围内，每头雌峰对马尾松毛虫、水青蛾和柞蚕剖腹卵的日破坏数（寄生数）分别力１５、１８和２６粒，一生破坏数分别为５６、９１和２０８粒。即使虫卵即将孵化，该峰同样亦能寄生，并羽化出正常的子代白跗平腹小蜂。     

马铃薯品种抗软腐病测定条件的研究

用全薯块吸头刺伤接种法测定时,较理想的测定条件为:每接种点接种0.1ml浓度为10~2～10~5CFU/ml菌悬液,随后在21±5℃～31±5℃(依所用菌株而定)下保持2～3天,以接种点腐烂斑的最大直径作记载标准。用新鲜薯片法测定时,除接种浓度为10~2～10~3CFU/ml,保持时间为1～2天及以侵染限值作评价标准外,其余条件和全薯块吸头刺伤接种法相同。当用皮孔浸渍法接种时,薯块在10_6CFU/ml菌悬液中浸5分钟,然后使薯块表面保持连续水膜,3～5天后测量薯块表面腐烂面积。上述3种方法都必须有20个以上重复,并使用大小一致、无伤无病的成熟薯块。     

火炬松短周期工业材不同高度上干缩性能的研究

对湖南同一立地指数（１８）下，５株１７．５年生的火炬松（ＰｉｎａｓｔａｅｄａＬ．）短周期工业材１．３，３．６，５．６，７．６，９．６ｍ５个高度的木材干缩系数、基本密度、生长轮宽度、晚材率和微纤丝角度，按生长轮取样，进行了测量和统计分析．结果表明，弦向、径向、体积干缩系数和干缩比，在树于５个高度之间的差异，均达到了显著水平；各高度干缩系数与生长轮的年龄（离髓心的距离）以及与上述各主要构造因子之间呈显著的线性相关，且相关度度随树干高度的增加而减弱．     

柑桔溃疡病发病程度对落叶、落果、果实大小及品质的影响

 雪柑叶片、果实溃疡病各病级的落叶率或落果率均随病级的增大而上升;而果实的大小和品质则随病级的增大而下降。除1级的落叶率、落果率、果实大小及品质与0级无显著差异外、其他各级均造成不同程度的大量落叶、落果、和果实变小品质变劣。探明病情指数与落叶、落果、果实大小及品质的关系,并分别建立回归模型。     

论嫩江流域水源涵养林工程布局

从维护东北老工业基地的生态安全出发,立足东四盟实际,着眼于对整个东北地区危害最大,影响范围最大的生态现象列为今后一个时期三北工程建设的战略重点,通过大量调研分析和借鉴专家意见,经筛选整合,初步确定未来东四盟地区三北防护林工程建设的战略重点。     

‘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.