侵染甘薯的烟草花叶病毒(TMV)

 甘薯由于甘薯病毒的普遍存在而造成大幅度减产。甘薯病毒种类复杂,主要有甘薯羽状斑驳病毒(SPFMV)、甘薯潜隐病毒(SPLV)、黄瓜花叶病毒(CMV)、烟草花叶病毒(TMV)。     

淡紫拟青霉菌料防治大豆胞囊线虫的后效研究

淡紫拟青霉不同菌株的培养菌料，施２２５ｋｇ／ｈｍ２，对大豆胞囊线虫不但当年有４５％～６９％的较好防效，而且第２年和第３年仍然有２２．５％～３７．７％和７．３％～２２．９％的后效，即空胞囊和被寄生的胞囊数量增加。     

春麦田除草剂的应用与杂草群落演替

作者采用定点定位试验,对春麦田除草剂应用与杂草群落演替趋势进行研究。结果表明:在杂草群落多样性麦田,小麦连作并分别连续5年施用同一种除草剂,原杂草群落中占优势的靶标杂草得以控制,而非靶标杂草和抗、耐药性杂草因失去竞争和制约对象而猖獗发展,发生量较原来增加几倍至几十倍,并形成优势种群,对小麦造成新的更严重的危害。一种除草剂在同田块连续施用4年,由于杂草群落演替,抗、耐药杂草兴起,除草效果显著下降而失去其使用意义。作者提出除草剂配套使用、轮用、混用等措施,并配合以合理的轮作制度,以减轻杂草群落长期受到单一的定向选择性压力。     

亚热带牧用草地中威提特东非狼尾草的种子繁殖研究

在3月和4月对全日制放牧的东非狼尾草草地上的风干牛粪取样,进行发芽试验,分别测定其中的东非狼尾草发芽种子数量。结果,3月取样平均432.5 g的牛粪中东非狼尾草平均发芽种子数量为118.25粒,4月取样平均437.8 g的牛粪中东非狼尾草平均发芽种子数量为52.8粒,二者平均牛粪重为435.15 g,平均发芽种子为85.5粒,说明牛粪中东非狼尾草种子数量较多,是其繁殖扩展较快的主要原因;3月取样的种子数量为4月取样数量的1.38倍,说明人工利用牛粪进行东非狼尾草繁殖时,需在有降雨来临前准备,即1～3月进行牛粪的准备工作。     

乳猪体内糖类的消化和吸收研究

乳猪小肠内葡萄糖的分布状况既与饲料的碳水化合物种类和数量相关，也与小肠的不同部位相关，十二指肠段和空肠段分别是乳糖、淀粉类碳水化合物分解和葡萄糖吸收的主要部位血糖浓度离肝脏越远含量越低，而与饲料中糖类含量的多少无关。     

兔病毒性出血症、多杀性巴氏杆菌病、产气荚膜梭菌病(A)型三联灭活疫苗研制

对 5批兔病毒性出血症、多杀性巴氏杆菌病、产气荚膜梭菌病三联灭活疫苗进行了动物试验 ,结果表明该疫苗安全有效。近期效检对兔病毒性出血症的保护率为 1 0 0 % ,对兔多杀性巴氏杆菌病保护率为 92 % ,对产气荚膜梭菌病 (A)型保护率为 88%。在免疫期试验中 ,免疫 6个月后 ,对兔病毒性出血症保护率为 1 0 0 % ,对多杀性巴氏杆菌病的保护率为 79% ,对产气荚膜梭菌病 (A)型的保护率为 88%。在保存期试验中 ,4～ 8℃保存 1年仍有效。     

长期施肥条件下菜田—蔬菜生态系统变化的研究( Ⅳ) 蔬菜生态系统的变化

 以2002 年设施番茄栽培为代表计算其N、P、K投入量与携出量之间的表观平衡状态, 其结果基本上和14.5 年后的土壤实测值与设施栽培本底值之间纵向比较的增长关系一致, 前者只能说明系统养分变化的趋势, 后者才是实际的养分盈亏状态, 养分盈亏主要取决于有机肥的施用与养分元素的供给。5个代表性处理模拟了蔬菜施肥的不同现状, 从土壤肥力及产量等方面的变化真实反映出各自的系统变化及发展趋势, 在本试验条件下以ANK施肥下的系统最优。对有机肥施用、化学肥料的配施以及测土施肥等问题进行了探讨。     

农业外来生物入侵种研究现状与发展趋势

目前国际上对外来生物入侵种的研究主要在个体水平上研究外来种对新环境的进化与适应,本地种对生物入侵后发生的进化调整;种群和群落水平上研究外来种的定居、潜伏、竞争和暴发;生态系统水平上研究生境的可入侵性和外来种对生态系统结构和功能的影响等几个方面。风险分析标准化与定量化、检疫鉴定快速化、除害技术安全化、信息管理全球化是全世界对外来物种入侵管理与科研的焦点问题。本文依据外来物种入侵的形成和扩散暴发过程,提出了超前预防和综合管理等未来需要解决的关键问题。     

Influence of Sini decoction on the proliferation and apoptosis of artery smooth muscle cells after balloon injury

AIM: To investigate the influence of Sini decoction (SND) on the proliferation and apoptosis of rabbit abdominal aorta smooth muscle cells after ballon injury and discuss the effect of vascular smooth muscle cell's (VSMCs) proliferation and apoptosis in post-percutaneous coronary intervention (PCI) restenosis (RS) and the feasibility of SND preventing post-PCI RS. METHODS: The animal model of rabbit abdominal aorta ballon injury was set up and the therapertic group was treated with SND. The shape of proliferative and apoptotic cell were investigated by electron microscope. Immunohistochemistry staining was performed using α-actin,PCNA and Cyclin E monoclonal antibodies. In situ Cell Death Detection Kit was used to identify apoptotic cells. Abdomial aorta angiography was operated in the 84th day subgroup and the stenosis degree was evalued by quantitative angiographic analysis. RESULTS: As compared with the control group, the therapeutic group displayed a lower proliferative percentage and a higher apoptosic percentage (P<0.05). Moreover, the apoptosic peek time was on the 14th day after operation,which was longer than the control group. CONCLUSION: SND effectly inhibited the proliferation of VSMCs and iuduced apoptosis in VSMCs.     

The molecular mechanism of inhibition of murine Lewis lung carcinoma metastasis by weimaining in vivo

AIM: To investigate the anti-metastasis effect of weimaining, extracted from fragopyrum cymosum meissn, a Chinese medicine, on murine Lewis lung carcinoma (3LL). METHODS: The anti-metastasis effect of weimaining in vivo was detected in the grafting lung metastasis model of murine Lewis lung carcinoma. The effects of the drug on the expression of CD34 and E-cadherin were investigated by immunohistochemical staining and RT-PCR. RESULTS: Weimaining effectively inhibited the lung metastasis of 3LL at a concentration of 250 mg·kg^-1·d^-1, significantly suppressed the expression of CD34 and increased the expression levels of E-cadherin protein and mRNA in 3LL cells. CONCLUSIONS: Weimaining inhibits the metastasis of murine Lewis lung carcinoma (3LL) in vivo via increasing the expression of E-cadherin and decreasing microvessel density of tumor tissue.