三唑酮种衣剂对小麦白粉菌侵染和非侵染位点硅等元素含量的影响

 借助扫描电子显微镜-X射线能谱分析方法从超微结构和元素水平观测了三唑酮种衣剂包衣处理和空白对照的小麦幼苗上白粉病菌侵染及非侵染位点硅等元素含量的变化。结果表明,接种后20~36 h内三唑酮种衣剂处理的麦苗侵染位点细胞内元素硅含量由5.204%上升为42.064%,非侵染位点由5.821%上升为12.342%;空白对照中侵染位点元素硅含量由低于检测水平上升为17.388%,非侵染位点接种后36 h时为19.460%。在处理和空白对照的麦苗上侵染和非侵染位点均检测到了含量不等的磷、硫、氯等元素存在。     

药剂拌种对春油菜白粉病和茎象甲的防效及对油菜产量的影响

为明确不同药剂拌种对春油菜出苗率、病虫害防效及产量的影响, 本文在3种不同种植密度下, 针对春油菜白粉病、油菜茎象甲, 选择25 g/L咯菌腈FSC、600 g/L吡虫啉SC、30%噻虫嗪SC、600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30%噻虫嗪SC+25 g/L咯菌腈FSC进行了拌种处理试验。结果表明, 各拌种处理对春油菜的出苗有一定的影响, 其中600 g/L吡虫啉SC、30%噻虫嗪SC、600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30% 噻虫嗪SC+25 g/L咯菌腈FSC拌种对春油菜出苗的影响大于25 g/L咯菌腈FSC拌种; 600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30%噻虫嗪SC+25 g/L咯菌腈FSC拌种对白粉病和茎象甲的防效均高于单剂拌种; 600 g/L吡虫啉SC+25 g/L咯菌腈FSC拌种, 对春油菜白粉病的最高防效可达59.3%, 30%噻虫嗪SC+25 g/L咯菌腈FSC拌种对油菜茎象甲最高防效可达69.2%。白粉病病情指数与春油菜种植密度呈正相关, 拌种防效随密度增加而降低, 综合产量分析, 最佳种植密度为28.5万～34.5万株/hm2。     

紫花苜蓿白粉病病原鉴定

通过对甘肃定西县一年生紫花苜蓿白粉病蜡叶标本上的白粉菌的显微观察和计测,该菌闭囊壳直径85.5～128.3 m,平均直径95.7 m。每个子囊壳附属丝平均数量为27条,多数为20～30条。每个子囊壳含子囊6～8个,多数为6个,子囊大小为85.5m32.1 m。子囊内有子囊孢子2～4个,绝大多数为2个。167个子囊孢子计测结果,大小为32.1～21.4 m。附属丝褐色,多数基生,少数侧生,菌丝状,长度为子囊壳直径的0.6～1.6倍。经鉴定苜蓿上的白粉菌为蓼白粉菌(Erysiphe polygoni DC.)     

Local and systemic resistance to fungal pathogens triggered by an AVR9-mediated hypersensitive response in tomato and oilseed rape carrying the Cf-9 resistance gene

Tomato and transgenic oilseed rape plants expressing the Cf-9 resistance gene develop a hypersensitive response (HR) after injection of the corresponding Avr9 gene product. It was investigated whether induction of a HR conferred resistance to different fungal pathogens in tomato and oilseed rape. Induction of an AVR9 mediated HR at the pathogen infection site delayed the development of the biotrophs Oidium lycopersicum in tomato and Erysiphe polygoni in oilseed rape, but enhanced the development of the necrotrophs Botrytis cinerea and Alternaria solani in tomato and Sclerotinia sclerotiorum in oilseed rape. Interestingly, delayed fungal disease development was observed in plant tissues surrounding the HR lesion regardless of whether a necrotrophic or biotrophic pathogen was used. In tomato, AVR9 injection induced systemic expression of PR1, PR2 and PR3 defence genes but did not induce systemic resistance to O. lycopersicum, B. cinerea or A. solani. In oilseed rape, AVR9 injection temporarily induced systemic resistance to Leptosphaeria maculans and E. polygoni, but did not induce detectable systemic expression of PR1, PR2 or Cxc750. These results give new insights into the potential uses of an induced HR to engineer disease resistance.     

Powdery mildew resistance in barley landrace material. I. Screening for resistance

A total of 4,681 accessions of Hordeum vulgare landrace material from Ethiopia, East Mediterranean, Near East, Nepal and China were sown in the field and subjected to the natural powdery mildew epidemic in Denmark. Apparently resistant accessions were selected. Selfed progeny from them were retested and reselected in subsequent years at four locations in Denmark. Finally, 16 promising donors of resistance were retained. They were characterized in the field and tested in the seedling stage for reaction to up to 72 different isolates of the powdery mildew fungus. The absence of the corresponding virulences in the Danish airborne powdery mildew population was ascertained in five years. The resistances in the 16 donors are apparently mutually different and from known sources of powdery mildew resistance in barley. This revised version was published online in July 2006 with corrections to the Cover Date.     

Identification of resistance gene analogue markers closely linked to wheat powdery mildew resistance gene Pm31

Specific oligonucleotide primers, designed for the sequences of known plant disease resistance genes, were used to amplify resistance gene analogues (RGAs) from wheat genomic DNA. This method was applied in a bulked segregant analysis to screen for the RGA markers linked to the powdery mildew resistance gene Pm31, introgressed into common wheat from wild emmer. Two RGA markers (RGA200 and RGA390) were found to be closely linked to Pm31 and completely co‐segregating with the marker allele of Xpsp3029 linked to Pm31, with a genetic distance of 0.6 cM. These two RGA markers were then integrated into the formerly established microsatellite map of Pm31 region. The result showed the effectiveness of the RGA approach for developing molecular markers linked to disease resistance genes and demonstrated the efficiency of denaturing polyacrylamide‐gel electrophoresis for detecting polymerase chain reaction polymorphism.     

Effectiveness of Twenty-Four Barley Resistance Genes Against Powdery Mildew (Erysiphe graminis DC f. sp. hordei Em. Marchal) in Spain

Twenty-four near-isogenic barley lines, with a cv.‘Pallas’ background, carrying different mildew resistance genes were subjected in 1987, 1989 and 1990 to natural infection by the pathogen at several different and contrasting Spanish sites in order to study its virulence. The virulence genes proved to be geographically grouped into three regions: western (Valladolid), southern (Sevilla) and northern and northeastern (Navarra, Lleida and Girona). The mildew population of Lleida was more variable when compared with Navarra and Valladolid. Overall, the most effective resistance genes were: Ml-a13 + Ml-(Ru3), mlo and Ml-(1402).     

Field assessment of partial resistance to powdery mildew in spring barley

Summary Partial resistance to powdery mildew in spring barley was evaluated in three plot types: large isolation plots, in 1.4 m² plots in chessboard design with guard plots of spring wheat and in single rows. Percentage leaf area covered by powdery mildew was scored four to six times during the season and partial resistance was characterized by the area under the disease progress curve. Varietal differences were revealed in al three plot designs, differences between the most resistant and susceptible genotypes being of a factor five. Differences between varieties decreased with decreasing plot size. The relationship between single scores of amount of powdery mildew on the upper four leaves and the area under the disease progress curve was high in all plot designs during the first two to three weeks after heading, allowing selection for the trait by one or two scorings. Differential ranking of varieties between different plot designs was observed, and is assumed to be due to increasing plot interference with reduced plot size and reduced distance between plots. A reliable selection for partial resistance could be made in large isolation plots and in 1.4 m² plots, but hardly in single rows.     

Genetic analysis of powdery-mildew (Erysiphe graminis f.sp. hordei) resistance derived from wild barley (Hordeum vulgare ssp. spontaneum)

The inheritance of resistance to powdery mildew was investigated in 20 accessions of Hordeum spontaneum and in 20 F₄ lines derived from crosses between the variety ‘Aramir’ and 13 accessions of H. spontaneum. Two resistance genes were detected in 17 accessions, and three resistance genes in one accession. In two accessions, only one resistance gene was present. The 20 breeding lines showed a large variation in infection type and infection level. The genetic relationship between the resistance genes detected was investigated in the seven most resistant F₄ lines. These F₄ lines were divided into three groups which carried different resistance genes. In two lines, the detected resistance gene was shown to be race-specific.     

Genetics of powdery mildew resistance in pea

The genetics of powdery mildew (Erysiphe pisi) resistance in pea (Pisum sativum) was studied using five isolates of E. pisi in a controlled environment. Resistance was controlled by a single recessive gene in all the pea cvs. included in the study. The same recessive gene controlled resistance to all the five isolates of E. pisi. Tests for allelism showed that resistance in cvs. HPPC-63, HPPC-95, DPP-26, DPP-54, Mexique-4, SVP-950, Wisconsin-7104 and P-6588 is conferred by the same recessive gene. This revised version was published online in July 2006 with corrections to the Cover Date.