According to the inoculative experiments in green house,the results showed that the latent period of soybean frogeye leaf spot was determined by the effective accumulative temperature for certain cultivars. The dynamic variation of daily rate of lesion appearance can be forecasted by the effective accumulative temperature. The paper showed that the relationship between the accumulative daily rate of lesion appearance and effective accumulative temperature of 3 cultivars might be described Gompertz model. The model of 3 cultivars are: Hongfeng 3 pp=104.2276exp[-29.9088exp(-0.06625TT)] r=0.9094 Hefeng 25 pp=106.1627exp[-33.6979exp(-0.06329TT)] r=0.9659 Suinong 8 pp=107.2370exp[-24.0048exp(-0.05851TT)] r=0.9439 respectively, in which pp is accumulative rate of symptom appearance,TT is effective accumulative temperature.
A filamentous virus isolate, CA, was isolated and identified from chrysanthemum showing mottle symptom in Beijing area. Chenopodium quinoa and Nicotiana tobacum ‘xanthi’ were the best indicator and propagation species. Isolate CA could be transmitted by Myzus persicae in non-persistant manner efficiently. The properties of crude sap were:TIP=50 -60℃, DEP=10-3-10-4,LIV=2~3 days. The purified CA preparetion contained flexuous particles 692nm in average and one type of coat protein of Mr 32.3×103. Pinweel and bundle inclusions were found in the infected leaf cells. CA antiserum with microprecipitin titer of 1:512 was obtained. The IgG was used for the ELISA test of tissue culture of chrysanthemum. According to the result of identification isolate CA is considered as a member of Po-tyvirus. The tests of double diffusion, Precipitin, Latex and ISEM demonstrated no sero-logical relationship between CA and PVY.
Purified PLRV, stems and leaves of potato plant, rose-end and heel-end of dormant tuber, sprouts of broken dormant tuber with secondary infection by PLRV and viruliferous Myzus persicae adults were detected by indirect enzyme linked immunosorbent assay (ELISA) on nitrocellulose membranes respectively. The results indicated that the minimum amount of purified PLRV as little as 45.83pg~4.583pg can be detected and PLRV can be detected in stems and leaves of infected potato plant, rose-ends and heel-ends of dormant tuber with secondary infection,sprouts of broken dormant tuber by Dot-ELISA at dilutions of 1/2048,1/512,1/2048-1/8192,1/512-1/2048 and 1/2048-1/8192 respectively. PLRV in viruliferous Myzus persicae adults can also be detected at least with dilution of 1/2.