对虾白斑综合征病毒研究概况

对虾白斑综合征病毒(WSSV)引起世界范围内养殖对虾的急性、致死性传染病,造成对虾养殖业的巨大损失,在我国这种情况尤为严重。WSSV是同一类紧密相关的无包埋体类杆状病毒,与杆状病毒并无同源性。2001年,中国和荷兰科学家分别报道了WSSV的全基因组DNA序列,启动了WSSV后基因组研究。已有多种检测方法用于WSSV的检测和致病机理的研究。WSSV感染宿主谱广,以多种传播途径感染宿主,目前还没有用于病毒增殖的细胞系,但已有成熟的动物模型,从而方便了对WSSV的研究。本文就该病毒的命名、病毒特性、检测方法、病毒感染增殖、感染宿主、传播途径及感染动物模型等方面的研究现状和进展作一综述。     

大枫子与马钱上的叶斑类真菌病害

报道1986～1989年在泰国大枫子、海南大枫子和印度马钱上发现的9种叶斑类真菌病害的症状、病原菌及病情、分布。9种病原菌中,大枫子褐斑病菌(Ascochyta hydnocarpi S.M.Lin et P.K.Chi)、马钱叶枯病菌(Didymosphaeria strychnoris S.M.Lin et P.K.Chi)、马钱叶斑病菌(Microsphaeropsis strychoris S.M.Lin et P.K.Chi)和马钱轮纹褐斑病菌(Mycosphaerella strychnoris S.M.Lin et P.K.Cki)是新种。     

糖槭叶枯病发病规律及防治

糖槭叶枯病 Phyllosticta negundinis病菌孢子放散开始期和高峰期与每年的温、湿度变化有关。病害发生严重程度与降雨量关系密切 ,降雨早且量大时病害严重。病菌以分生孢子器和分生孢子在病叶上越冬 ,通过气流传播成为翌年初侵染源。喷洒 70 %甲基托布津可湿性粉剂 10 0 0倍液和 75%百菌清可湿性粉剂 80 0倍液均能收到较好的效果     

MapInfo在基准地价评估成果图中的应用实践

本文以MapInfo7.5作为GIS的平台软件,将MapInfo用于基准地价评估成果图的信息管理,利用创建、修改或更新的相关表格,建立相应的专题地图,使成果图中的信息更加直观明了。实践证明,MapInfo为基准地价评估成果图的及时更新、科学管理、有效利用提供了可靠的途经。     

中国水果供给结构性变化的实证研究

为分析中国水果供给的结构性变化，本文构造中国水果的供给模型，将1978-2001年24年划分为两个时期，利用Chow检验分别回归后发现我国水果供给的各种弹性均发生了明显的结构性变化，从而得出果农对价格的反应能力和敏感性增强、对农资投入的依赖性增强等重要结论。     

一次防治大豆灰斑病籽粒灰斑

通过室内及田间大豆不同生育期接种试验证明，籽粒感染灰斑病的关键时期是Ｒ３－Ｒ５期．Ｒ２期以前侵染不造成籽粒斑驳，据此提出一次防治大豆籽粒灰斑病的关键时期为Ｒ２－Ｒ４期．     

我国价格体系改革趋势初探

本文以我国国民经济系统与河南省经济子系统的同构性为基础,利用河南省1987年投入产出表,计算出诺依曼最优生产强度和与之相应的最优价格,进而对照现行价格,提出了我国价格体系改革走向的基本构想,并对其合理性、可行性进行了初步研究。     

Morphological characterization of the interaction between Diplocarpon rosae and various rose species

Blackspot, caused by Diplocarpon rosae , is the most severe and ubiquitous disease of garden roses, but information is lacking about genotype-specific forms of resistance and susceptibility of the host. Macro- and microscopic analyses of 34 rose genotypes with a defined monoconidial culture black spot inoculum identified susceptible and resistant rose genotypes and further genotype-specific subdivisions, indicating the presence of partial forms of resistance and different resistance mechanisms. In total, eight interaction types were characterized, five representing compatible (types 1–5) and three representing incompatible interactions (types 6–8). The incompatible interactions were characterized by the lack of any visible fungal structures beneath the cuticle (type 8), single-cell necroses (type 7) or necroses of larger cell clusters (type 6), the latter two types with penetration hyphae and haustoria in epidermal cells.     

Pelargonium flower-break and pelargonium line pattern viruses in the Netherlands; purification,antiserum preparation,serological identification,and detection in pelargonium by ELISA

Two viruses, detected frequently in the Netherlands in pelargonium, were identified by serology and test plant reactions. Antisera were prepared and an ELISA procedure was developed to detect the viruses in pelargonium.One of the viruses, PFBV-N, proved to be pelargonium flower-break virus. With the antiserum to PFBV-N, it could be detected reliably throughout the year inPelargonium zonale Springtime Irene.The other virus, PLPV-N, was serologically closely related to pelargonium line pattern virus (PLPV) and to pelargonium ring pattern virus (PRPV), as were an old virus isolate from Saturnus, collected in the Netherlands in 1971 (L128), and PLPV isolates from Yugoslavia (PLPV-Y) and Denmark (PLPV-D). There were only minor differences in host-plant reactions between the virus isolates. Based on these tests, PLPV and PRPV are considered as isolates of the same virus, for which, for practical reasons, the name pelargonium line pattern virus is proposed.PLPV could be reliably detected by ELISA inP. zonale Springtime Irene and Amanda throughout the year with only a few exceptions. InPelargonium peltatum Tavira, however, reslts were erratic due to uneven distribution of virus in the plant. Best results were obtained when petioles of fully expanded leaves were tested.     

Detection of airborne inoculum of Leptosphaeria maculans and Pyrenopeziza brassicae in oilseed rape crops by polymerase chain reaction (PCR) assays

The potential use of DNA-based methods for detecting airborne inoculum of Leptosphaeria maculans and Pyrenopeziza brassicae , both damaging pathogens of oilseed rape, was investigated. A method for purifying DNA from spores collected using Hirst-type spore samplers and detecting it using polymerase chain reaction (PCR) assays is described. For both pathogens, the sensitivities of the DNA assays were similar for spore-trap samples and pure spore suspensions. As few as 10 spores of L. maculans or P. brassicae could be detected by PCR and spores of both species could be detected against a background of spores of six other species. The method successfully detected spores of P. brassicae collected using spore traps in oilseed rape crops that were infected with P. brassicae. Leptosphaeria maculans spores were detected using spore traps on open ground close to L. maculans -infected oilseed rape stems. The potential use of PCR detection of airborne inoculum in forecasting the diseases caused by these pathogens is discussed.