澳洲淡水龙虾高效生态养殖技术

澳洲淡水龙虾又名红螯螯虾(Cherax guadricarinatus),原产于澳洲北部的热带、亚热带水域中,是目前世界上最名贵的淡水经济虾类之一。为了探索和推广澳洲淡水龙虾高效生态养殖技术,笔者于2004年4月在福建漳州罗氏沼虾养殖场进行澳洲淡水龙虾养殖试验,并通过了验收。一、养殖池的条件养殖池共计2排,每排均有11口养殖池,每口养殖池面积均为4000m2,即养殖池总面积为88000m2。养殖池为长方形,东西走向,长宽比例为3∶1,深度为1.8m,池底平坦且略向排水一侧倾斜,底质为泥沙质,池底有1/3面积种植水草。养殖池进排水方便,水源充足,水质良好。每口养殖…     

高寒草甸退化草地—“黑土滩”植物量测定

依据高寒草甸草地秃斑地的多少和距居民点的远近划分为轻度退化草地(极少量秃斑地)、中度退化草地(少量秃斑地)、重度退化草地(大量秃斑地)和极度退化草地(全部秃斑地)四个退化草地等级。对各等级退化草地进行了植物量测定。结果表明:草地植物量(地上和地下)及土壤含水量,随着草地退化程度的加剧明显下降(P<0.01),毒杂草量则明显上升(P<0.01)。其中极度退化草地较轻度退化草地植被中嵩草属牧草优势度减少38,可食鲜草量减少219.2g/m~2,而毒杂草则增加99.6g/m~2,植物活根量(干物质)减少2390.6g/m~2,土壤含水量(0—10cm)减少10.02％,并对高寒草甸退化草地(黑土滩)的成因及治理途径提出了看法和意见。     

水稻不育系粒黑粉病普遍率与严重度间的关系

 稻粒黑粉病(病原菌Neovossia horrida (TaK.)Padw. et A. Kahn)是杂交稻繁殖制种田不育系上的主要病害,流行频率高,危害损失大。普遍率和严重度的关系(I-S关系)是植病流行学观测技术上的一个重要问题。     

糖类寄生螨快速分离检验方法

本文对糖类寄生螨的快速分离检验方法进行了改进。将糖类溶解后，经过500目/英寸标准检验筛进行过筛分离。此方法对各种可溶性糖类中的寄生螨类能取得100％的快速分离检验结果。     

"双链型"草-鹅-稻生态农业模式高产高效配套技术

提出了“双链型”单-鹅-稻生态农业模式，总结了稻田套种牧草的方法和田间管理技术，探讨了种草与养鹅在时间上的相互衔接，以提高牧草的产量和利用率，进行了稻田套种牧草养鹅与种植小麦的比较效益分析。该配套技术的实施，为当前开展农业结构调整开辟了一条新路。     

溴隐停对惠州麻肉种鸡产蛋性能的影响

研究目的在于探讨多巴胺受体激动剂(溴隐停)对地方良种肉鸡繁殖性能的影响。方法从628只28周龄健康的“惠州麻”黄羽肉种鸡群中随机选取1组鸡笼内的40鸡作为实验组,其余的作为对照组。实验组鸡群喂服溴隐停,每只鸡每天1.25mg,连用4d,停用4d后再用4d,对照组不使用。结果在4周的实验期内实验组和对照组的产蛋率分别为83.86%和69.96%;破蛋率分别为1.28%和1.69%,畸形蛋率分别为4.33%和1.19%;实验组平均每只鸡的产蛋总数比对照组多3.89个、合格种蛋数多3.26个;药物处理对平均蛋重无显著影响;使用溴隐停能够提高鸡血液中的雌激素水平。结论溴隐停能够通过抑制地方良种肉鸡体内促乳素的合成与分泌,减少抱窝现象的发生,提高其繁殖性能。     

中蜂品系间杂种优势利用研究初报

经过冬蜜花期对以湖北鄂西中蜂为母本、广东粤东地中蜂为父本的杂交一代与本地中蜂进行比较，结果表明：杂交一代的繁殖力和产蜜量分别比本地中蜂高4．4％和11％。夏季乌桕花期对回交代进行对比结果表明：其繁殖力和产蜜量分别比本地中蜂高6％和21％。     

2型猪链球菌的血清学鉴定

本试验首次证实了２型猪链球菌在我国的存在，采用玻片凝集、琼脂扩散及毛细管沉淀等３项试验，对１９９０年以来广东某猪场断奶仔猪暴发流行的败血症、脑膜炎及关节炎病猪中分离的１５株链球菌进行了血清学鉴定。结果表明：１５株链球菌均为２型猪链球菌；用高压法提取抗原进行沉淀反应，其结果比酸热法提取抗原具有简便、敏感、特异性强的特点。     

“火罐”柿减压处理、低乙烯MA贮藏技术研究

利用减压贮藏的原理,提出了减压处理低乙烯ＭＡ贮藏技术,并利用该技术对陕西优良柿子品种－－火罐柿进行了室温条件下的保鲜贮藏研究。结果表明,减压处理低乙烯ＭＡ贮藏技术甬地抑制火罐柿硬度的下降,延长果实贮藏期。保硬期为４３ｄ,比对照长２４ｄ;贮藏期达９７ｄ,比对照长６７ｄ。     

‘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.