解淀粉芽胞杆菌TS-1203对苹果炭疽叶枯病菌的抗生作用

为明确解淀粉芽胞杆菌TS-1203对苹果炭疽叶枯病菌的抗生作用, 采用平板对峙法和菌丝生长速率法以及孢子萌发法测定了解淀粉芽胞杆菌TS-1203对苹果炭疽叶枯病菌菌落生长和孢子萌发的抑制作用?结果表明:菌株TS-1203对苹果炭疽叶枯病菌具有显著的抑制作用, 其菌液对病菌的抑制率高达70.4%; 其发酵液对苹果炭疽叶枯病菌的抑制率随着发酵液浓度的增加而升高, 尤其当发酵液浓度为15%时, 其抑菌率为 59.0%; 发酵液处理苹果炭疽叶枯病菌孢子24 h后, 其萌发抑制率与芽管生长抑制率分别为78.2%与64.3%, 且芽管出现畸形; 利用TS-1203发酵液处理苹果离体叶片后接种炭疽叶枯病菌, 其防效为70.1%?综合分析表明, 解淀粉芽胞杆菌TS-1203对苹果炭疽叶枯病菌具有良好的抑制作用?     

海洋霉菌1-B6-10代谢产物对几种镰刀菌的抑制作用

测试了海洋霉菌菌株1-B6-10代谢产物对不同镰刀菌菌丝生长、孢子萌发和显微形态的影响.结果表明,该菌代谢产物粗提物对尖孢镰刀菌Fusarium oxysporum菌株F1113、F1125和番茄镰刀菌Fusarium batatasis菌株F2016等的菌丝生长具有明显的抑制作用.当纸片上滴加0.05 mL该粗提物时,其抑菌圈直径均在32 mm以上;在菌株F1125菌丝块上直接滴加0.05 mL该粗提物,其菌丝生长抑制率达到98.39%.该代谢产物也能显著抑制尖孢镰刀菌F113和F1125孢子的萌发,用粗提物处理后培养48h,其孢子萌发率仅为8%和9.6%.显微镜观察结果表明,在添加该代谢产物亚抑菌浓度的培养基中,尖孢镰刀菌F1113菌丝的形态发生改变,部分菌丝萎缩和断裂.     

香蕉枯萎病拮抗菌的筛选及其作用机制研究

通过分离和筛选,从香蕉园或者其他果园的土壤中分离获得13株对香蕉枯萎病菌(Fusarium oxysporum f.sp.cubense)具有抑制作用的拮抗菌,并对部分拮抗菌抑制病菌菌丝生长和孢子萌发进行了试验。结果表明,拮抗菌株d4、d5、B3和p发酵液对香蕉枯萎病菌生长具有显著的抑制作用,在平板上产生的抑菌圈直径为21.75～34.75 mm,抑菌效果具有持续稳定性,对孢子萌发的抑制率为90.49%～97.18%;拮抗菌对病菌的作用表现为对菌丝的消融、菌丝细胞的泡囊化、抑制病菌分生孢子的萌发、孢子芽管的扭曲。     

拮抗细菌菌株BC98-I对青椒枯萎病菌的抑制作用

拮抗细菌菌株BC98-I是从沤肥浸渍液中分离筛选到的一株对青椒枯萎病菌Fusarium oxysporum f.sp. vasinfectum具有强烈抑制作用的蜡质芽孢杆菌。菌含量为5.0×108 cfu/mL的该拮抗菌发酵液在平皿上对青椒枯萎病菌的抑制率为91.7% ±0.5%;该发酵液经高温高压灭活后对青椒枯萎病菌仍有抑制作用,抑制率为58.3% ±2.2%。经硫酸铵沉淀从发酵液中粗提到对青椒枯萎病菌具有抑制作用的拮抗蛋白粗提物,经孔碟法试验表明,浓度从5 ~60 mg/mL的粗提物对病原菌的抑菌圈直径达12 ~27 mm。显微观察显示:拮抗蛋白粗提物可造成青椒枯萎病菌菌丝异常;对孢子的抑制作用主要表现为孢子萌发产生的芽管短,部分芽管膨大形成大泡囊。该拮抗蛋白对热、蛋白酶、氯仿稳定;耐酸碱,对紫外线和离子强度部分敏感。     

链霉菌182-2抗真菌活性物质的分离及抑菌特性的初步研究

[目的]链霉菌182-2的发酵液对烟草赤星病有良好的抑制作用,本文拟对其发酵液中抗真菌活性组分进行初步分离,并进行抑菌特性研究.[方法]发酵液经预处理后,依次用活性炭脱色,大孔树脂吸附层析分离纯化,对纯化后活性物质(组分Ⅱ)的抑菌活性进行测定.[结果]分离纯化结果表明其活性物质中至少含有两种抗真菌活性组分.离体条件下当活性物质浓度为2 000μg/mL时,对烟草赤星病菌有很强的抑菌作用,抑菌圈直径达58.0mm.目测法测定抗生作用表明其最小抑菌浓度(MIC)为80 μg/mL,最小杀菌浓度(MBC)为160μg/mL.48 h时对菌丝生长和孢子萌发的抑制率最高,抑菌中浓度(EC50)分别为31.9 μg/mL和42.2μg/mL.活性组分处理还可导致病原菌菌丝和孢子萌发产生的芽管变形扭曲或产生大泡囊.[结论]纯化后的活性物质对烟草赤星病菌具有较强的抑制作用,有进一步研究利用的价值.     

致病杆菌CB43菌株对灰霉病菌的抑制作用

测定了致病杆菌CB43菌株代谢物对灰葡萄病菌菌丝生长和孢子萌发的影响。结果表明:CB43代谢物对灰葡萄孢菌丝生长有较强的抑制作用,500、250、125ml/L代谢物能完全抑制菌丝的生长,并具有杀死作用。62.5ml/L的发酵液处理灰葡萄病菌菌丝72h的抑制率仍达83.35%。20ml/L的发酵液处理灰葡萄孢菌丝能引起菌丝畸形,异常分支、粗短。CB43代谢物能杀死灰葡萄孢分生孢子或抑制其萌发,500~62.5ml/L的发酵液处理16h后,孢子萌发抑制率达88.1%~97.91%。温室试验表明,CB43代谢物对黄瓜灰霉病的控制效果达84.09%,化学农药40%施佳乐的效果为72.94%。     

胶孢炭疽菌生防放线菌gz-8的鉴定及生物活性初步评价

从山东省临沂地区土壤中分离到一株放线菌gz-8,发现其对胶孢炭疽菌Colletotrichum gloeosporioides具有较强的抑制作用,皿内抑菌活性达72.5%。通过形态特征和生理生化测定,结合16S rDNA序列分析,鉴定该菌株为栗褐链霉菌Streptomyces badius。抗菌谱测定结果表明,菌株gz-8对6种植物病原真菌均具有较强的抑菌活性,抗菌谱较广。进一步对菌株gz-8的粗提物进行了生物活性评价,发现其发酵液粗提物可以明显抑制胶孢炭疽菌的菌丝生长（EC50=3.18 μg/mL）和分生孢子萌发（IC50=1.92 μg/mL）,且活性明显高于菌体粗提物;同时发酵液粗提物具有良好的热稳定性及pH稳定性;1 000 mg/L的发酵液粗提物对感染胶孢炭疽病芒果果实的防效达到35.94%,与同浓度下百菌清的防效（34.11%）无显著差异。     

链霉菌Sa-21对烟草黑胫病的防效及抑菌作用研究

烟草疫霉引起的烟草黑胫病,是烟草生产上的重要病害之一。为了明确链霉菌Sa-21防治烟草黑胫病的应用潜力,用盆栽试验测定了链霉菌Sa-21的生防效果,并用生长速率法等手段探讨了链霉菌Sa-21对烟草疫霉的抑菌作用。盆栽试验表明,链霉菌Sa-21菌株发酵液对苗期和成株期烟草黑胫病有较好的控制效果,最高防效可达98.39%。菌株Sa-21粗浸膏对烟草疫霉菌丝生长的抑菌中浓度为56.1 μg/mL,50 μg/mL的粗浸膏处理后可以降低50%的菌丝生物量。菌株Sa-21粗浸膏对烟草疫霉孢子囊的产生、游动孢子释放、休止孢萌发以及细胞膜透性均有抑制作用,100 μg/mL的粗浸膏基本能够完全抑制孢子囊的产生,并且对游动孢子释放的抑制率达50%以上;粗浸膏浓度为150 μg/mL时,对休止孢萌发的抑制率达94.35%;随着粗浸膏浓度增加,菌丝细胞膜的透性也会加大。研究结果表明,链霉菌Sa-21代谢物对烟草疫霉的生长繁殖产生抑制作用,并为链霉菌Sa-21生防菌剂的开发及其对烟草黑胫病的防治提供了理论依据。     

嗜线虫致病杆菌代谢物对马铃薯晚疫病菌的抑制作用

采用室内以抑制法测定的结果表明：嗜线虫致病杆菌发酵液对马铃薯晚疫病菌有很强的抑制生长作用,６￣５０ｍｌ／Ｌ的发酵液对菌丝生长的抑制率达９０％￣１００％,１．５￣３ｍｌ／Ｌ的发酵液仍有７０％左右的抑制效果。发酵液对菌丝生长有抑制作用,但不能完全杀死菌丝;发酵液对孢子囊萌发也有一定的抑制作用,５０ｍｌ／Ｌ的发酵液对孢子囊萌发的抑制率达５０％;发酵液在２４小时内能渗透到种薯内３ｃｍ,抑制薯块内病菌的生长     

大蒜根系分泌物对烟草镰刀菌根腐病的控制作用

为探讨大蒜根系分泌物对烟草尖孢镰刀菌的抑菌活性,采用琼脂法培养大蒜,利用气相色谱—质谱技术（GC-MS）测定其主要成分,研究大蒜根系分泌物对烟草尖孢镰刀菌根腐病的影响。对菌丝生长速率和孢子萌发的测定表明,当大蒜根系分泌物粗提物浓度为1 g/mL时,其菌丝生长抑制率为30.56%,孢子萌发抑制率高达100.00%。大蒜根系分泌物主要成份2,6—二异丙基苯酚和邻苯二甲酸二丁酯分别对其菌丝生长和孢子萌发具有较强的抑菌作用。邻苯二甲酸二丁酯的防控效果较好,其浓度为5 mmol/L,接菌21 d后其病情指数为55.00,防控效果达32.38%。大蒜根系分泌物及主要成分对尖孢镰刀菌所引起的烟草根腐病有显著的抑制作用,这为研制含大蒜成分的植物保护剂和间作套种大蒜防控烟草尖孢镰刀菌根腐病提供科学参考。     

福寿螺配偶个体大小选择性初步观察

通过野外观察与实验研究,掌握了福寿螺的婚配体制及其配偶选择性规律。福寿螺与多数低等动物一样,其婚配属于乱交制,无固定配偶;雌螺对与其交配的雄螺个体大小没有选择性,而雄螺对雌螺的个体大小有选择性,倾向于与较大个的雌螺交配。     

厚朴病虫害种类的初步调查

采用标准地法和线路调查法,对湖北恩施市新塘乡双河厚朴基地的厚朴病虫害进行了系统调查,记录主要虫害13种,其中叶部害虫9种,枝干害虫2种,根部害虫2种。厚朴主要病害5种。藤壶蚧、厚朴枝角叶蜂和厚朴新丽斑蚜为湖北省首次报道,小绿叶蝉为厚朴新寄主记录种。同时记录了藤壶蚧的天敌6种,其中寄生小蜂2种,瓢虫4种;厚朴新丽斑蚜的天敌昆虫8种。对藤壶蚧、厚朴枝角叶蜂和厚朴苗木根腐病等重要病虫害的发生规律进行了初步调查,同时提出了防治建议。     

Localization of metabolic sites of action of herbicides

Time- and concentration-course studies were conducted to determine the effect of thirteen herbicides on photosynthesis, respiration, RNA synthesis, protein synthesis, and lipid synthesis using isolated single leaf cells. Each herbicide was from a different chemical class. Appropriate ¹⁴C-substrates and product purification procedures were used for each process prior to liquid scintillation counting. The most sensitive metabolic site of inhibition was photosynthesis for atrazine, bromacil, dichlobenil, monuron, and paraquat; RNA synthesis for dalapon and dinoseb; protein synthesis for chlorpropham; and lipid synthesis for CDAA, chloramben, 2,4-D, EPTC, and trifluralin. However, with several herbicides, one or more process was almost as sensitive as the one mentioned above. All herbicides inhibited more than one process, and the most sensitive site of inhibition may not be the same process that was inhibited the greatest at the maximum concentration and maximum exposure time used. Therefore, a concept of metabolic sites of action, rather than a primary site of action, appears to be more meaningful for herbicides.     

Effects of timing and method of application of Penicillium oxalicum on efficacy and duration of control of Fusarium wilt of tomato

The effects of timing and method of application of Penicillium oxalicum on the control of fusarium wilt of tomato were investigated. Application of P. oxalicum to tomato seedlings in seedbeds reduced disease caused by Fusarium oxysporum f.sp. lycopersici in a growth chamber by 45–49% and in glasshouse experiments by 22–69%. Disease suppression was maintained for 60–100 days after inoculation with the pathogen in the glasshouse. No disease reduction was observed in tomato plants where P. oxalicum was applied to seeds. Treatment with P. oxalicum did not affect the population of F. oxysporum f.sp. lycopersici in the rhizosphere.     

Mode of action of meturine

The effect of meturine on the light processes of photosynthesis was studied.Meturine is a herbicide for weed control in potato and cotton crops. It is a N-phenyl—N-hydroxy—N′-methylurea.The experiments were carried out on isolated pea and spinach chloroplasts.When examining photosystem I, reduced DPIP was used as an electron donor, whereas methyl-viologen served as an electron acceptor. When examining photosystem II, DPIP represented the electron acceptor.The obtained experimental results have pointed to the absence of the effect of meturine upon the photoreaction I.Unlike N-phenyl—N′, N′-dimethylureas (CMU, DCMU) meturine has been a very weak inhibitor of photoreaction II.The authors explain the photoreaction II inhibition of chloroplasts from plants treated with herbicidal doses of meturine by conversion of N-phenyl—N-hydroxy—N′-methylurea into Hill reaction inhibitor(s). N-Phenyl—N′-methylurea can be one of such meturine metabolites.Meturine herbicidal action is accounted for by meturine transformation into Hill reaction inhibitor(s) in the plant tissues.     

Mode of action of etoxazole

The mode of action of the 2,4-diphenyl-1,3-oxazoline acaricide/insecticide etoxazole has been argued to be moulting inhibition, but experimental results supporting this hypothesis are lacking. This study investigated the effect of etoxazole on chitin biosynthesis in the fall armyworm, Spodoptera frugiperda (Smith) (Lepidoptera: Noctuidae). Etoxazole induced moulting defects in fall armyworm larvae similar, if not identical, to those caused by benzoylphenylureas, a well-known class of insecticidal chitin biosynthesis inhibitors. Furthermore, in contrast to untreated larvae, the chitin content in the integuments of larvae several days after treatment did not differ from that in freshly ecdysed individuals, thus suggesting strong chitin biosynthesis inhibition in vivo. A more detailed investigation of the inhibitory potential by incubating cultured integument pieces from larvae of S. frugiperda with [14C]N-acetyl-D-glucosamine, a radiolabelled chitin precursor, revealed I50 values of 2.95 and 0.071 microM for etoxazole and triflumuron respectively. The incorporation of radiolabel into potassium hydroxide-resistant material was inhibited by etoxazole in a dose-dependent manner. Based on these results, it is concluded that the acaricidal and insecticidal mode of action of etoxazole is chitin biosynthesis inhibition.     

Measures of durability of resistance

ABSTRACT Conventional models for the durability of resistant cultivars focus on the dynamics of the frequency of resistance genes. This leads to a definition of the durability of resistance as the time from introduction of the cultivar to the time when the frequency of the virulence gene reaches a preset threshold. It is questionable whether this is the most appropriate way to measure durability. Here we use a simple epidemiological model to link population dynamics and population genetics to compare three measures of durability: (i) the expected time until invasion of the virulent genotype, by mutation or immigration, and subsequent establishment of a population (T(invasion)); (ii) the virulence frequency related measure of the time for the virulent genotype to take-over the pathogen population ( T(take-over)); and (iii) the additional yield, measured by the additional number of uninfected host growth days (T(additional)). Specifically, we show how the measures of durability are affected by deployment and epidemiological parameters. We use a combination of numerical solution and analytical approximation of a model for the population dynamics of avirulent and virulent genotypes of a pathogen growing in dynamically changing populations of resistant and susceptible cultivars. The three measures of durability are compared. Some consequences of the results for durable resistance in multilines and mixtures and the regional deployment of resistant cultivars are discussed.     

甲基硫菌灵标样的制备

本文介绍了用进口甲基硫菌灵样品，采用溶剂萃取，高速离心，重结晶，高效液相色谱，红外光谱等分析方法进行系统分离与鉴定，得到其标样的方法。     

Systems of designation of pathotypes of plant pathogens12

A variety of systems of designation has evolved to name pathotypes of plant pathogens. The systems were evaluated to determine those best suited for particular purposes. Virulence and avirulence/virulence formulae of pathotypes have advantage over the use of consecutive numbers or letters given in chronological order of pathotype discovery. As soon as pathotype information exceeds a certain level of complexity, mathematical codes are most advantageous, in particular two codes, octal notation and coded triplets. A more universal adoption of the most appropriate codes is recommended to ease communication and comparisons of results.