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1.
黄瓜黑星病侵染和发病规律及其生态防治的研究   总被引:11,自引:0,他引:11  
黄瓜黑星病菌以菌丝体在病残株内于田间或土中越冬,成为第二年初侵染来源。黄瓜种子内的菌丝也可越冬,带菌率最高可达37.76%。种子各部位均可带菌,以种皮为多。接种试验证明黄瓜黑星病菌主要是从叶、茎、果实的表皮直接穿透侵入,也可从气孔或伤口侵入,但极少。黄瓜黑星病菌的分生孢子产生必须具备90%以上的相对湿度(RH)和15℃以上的日平均温度。分生孢子在5—30℃下均可萌发,适温15—25℃,但萌发必须有水滴,在无水滴的情况下即使RH达100%也不能萌发。吉林省大棚内发病重是由于5月中旬以后棚温达到黑星病菌生长的温度范围,RH长时间(12小时以上)在90%以上。露地黄瓜黑星病的发生则与当年的降雨量和降雨日数多少有关。大棚内采用降低湿度的生态防治措施,可有效地控制病情,从而减少喷药次数而达到防治目的。  相似文献   

2.
稻曲病的接种技术研究   总被引:23,自引:0,他引:23  
 探索在田间条件下进行稻曲病的人工接种技术。通过比较3种接种体发现,上年保存于-20℃的厚垣孢子不能引起发病;用PS液体培养获得的薄壁分生孢子可引起发病,孢子浓度越高引起病穗率越高;菌丝片段-分生孢子混合液接种发病最严重。病原菌的培养菌龄对接种效果有影响。在水稻的3个时期接种,以抽穗破口前6~9d的效果最好。在一天的3个时段接种,以下午4~6时的病情最重。在接种液里添加马铃薯煮汁可显著提高接种发病率。本文的接种技术能高效引发稻曲病,最高穗发病率100%,最大病情指数93.96,最多穗病粒数110粒。该接种技术可鉴别出品种抗病性的差异。  相似文献   

3.
研究了油菜秸秆作为基质培养植物病原菌核盘菌的重寄生菌盾壳霉分生孢子,并从盾壳霉分生孢子萌发及其抑制核盘菌菌核子囊盘萌发等方面评价了所获得的盾壳霉分生孢子的质量。结果表明:盾壳霉野生菌株Chy-1和Zs-1,以及Chy-1的突变菌株SV-5-2(抗杀菌剂vin-clozolin)可以利用油菜秸秆为基质进行培养,有利于3个菌株的菌丝生长、分生孢子器及分生孢子的产生,分生孢子产量可达2·4×109~3·4×109个孢子/g干秸秆。水分含量和发酵时间影响盾壳霉分生孢子产量。在接种量为5×105个孢子/g干秸秆的条件下,以干秸秆中含水量为3~6ml/g,在20℃下发酵12d较为适宜。水琼脂平板试验表明:在20℃下培养48h,盾壳霉分生孢子的萌发率达到90%以上。将油菜秸秆基质培养的盾壳霉分生孢子接种于土壤中,无论是夏季试验,还是秋季试验,对核盘菌菌核萌发及存活具有显著的抑制作用。2003年夏季,4·0×106个孢子/m处理其核盘菌菌核萌发数比对照减少26·3%;秋季该处理比对照减少57·1%~88·0%。  相似文献   

4.
芦笋茎枯病发生规律及防治研究   总被引:2,自引:0,他引:2  
芦笋茎枯病菌以分生孢子器在病株残茬上越冬,成为翌年发病的主要初侵染源。分生孢子释放高峰为4月26日至7月9日。分生孢子释放、萌发、侵染必须在有水的条件下进行。孢子萌发需有芦笋组织液做营养激发,在清水中不萌发。病菌从侵入到形成新的分生孢子一个侵染周期在23—27℃为10—12天,17—22℃为15—20天。采笋田茎枯病发生发展经过扩展期(7月—8月上旬),盛发期(8月中旬—9月)两个阶段。雨日雨量是决定茎枯病消长流行的主导因素,降雨后5—7天田间即出现一次新侵染高峰,大雨或连阴雨后尤为明显,秋季早上植株结露有利茎枯病菌后期侵染。在化学防治上,日本产别腐烂(Befran)和国产复方多菌灵胶悬剂是防治芦笋茎枯病较理想药剂。  相似文献   

5.
 近年来,甘肃省白银市靖远县的一些砂田西瓜中出现了严重的叶疫病,严重田块病株率超过70%。2018年7月,从靖远县高湾乡罹病西瓜叶片上分离得到拟多隔孢属Stagonosporopsis真菌,病叶检出率达100%。采用离体叶片和植株接种法评价单孢分离菌株XG-3对西瓜和甜瓜的致病性,所有接种处理在24 h内均发病显症而对照未发病,其中发病叶片原接种菌的检出率为100%。菌株XG-3在PDA和OA平板培养基上20和25 ℃培养20 d,未见产孢。在自然感病的西瓜叶片上观察到少量分生孢子器,在人工接种发病的西瓜和甜瓜茎、叶上产生大量分生孢子器和分生孢子:分生孢子器球形至亚球形,大小为(82.4~243.3) μm×(82.4~188.4)μm,分生孢子器具1~2个孔口,孔口直径15.7~27.5 μm;分生孢子无色,0~3个隔膜,杆状、柱状、长椭圆形、花生形及不规则形,直或稍弯曲,分隔处不缢缩或缢缩,大小为(5.2~28.3)μm×(2.2~6.0)μm,分生孢子形态和大小依基质和环境条件的不同而有较大差异。BLASTn分析结果显示,菌株XG-3(GenBank登录号:MW282128)的rDNA-ITS序列与瓜拟多隔孢Sta. cucurbitacearum分离物287ITS(GenBank登录号:AY293804.1)的序列相似性达99.80%。在基于rDNA-ITS构建的系统发育树中,菌株XG-3与Sta. cucurbitacearum聚为一组,与西瓜拟多隔孢Sta. citrulli和木瓜拟多隔孢Sta. caricae区分开来。依据病菌形态学和分子生物学特征,将菌株XG-3鉴定为瓜拟多隔孢Sta. cucurbitacearum [Basionym: Sphaeria cucurbitacearum]。  相似文献   

6.
白粉寄生孢寄生黄瓜白粉菌的特性研究   总被引:1,自引:0,他引:1  
采用白粉寄生孢(Ampelomyces quisqualis Ces.AQ)接种离体条件下赛璐酚上黄瓜白粉菌[Sphaerotheca fuliginea (Schlecht)Poll.]和活体条件下黄瓜白粉菌后,通过棉兰染色和显微观察分析,初步明确了白粉寄生孢的侵染寄生过程。白粉寄生孢分生孢子产生芽管可入侵黄瓜白粉菌的分生孢子、菌丝、分生孢子梗;有时黄瓜白粉菌串生的分生孢子、分生孢子梗可被2~3条白粉寄生孢的菌丝寄生,随着寄生过程的进一步发展,黄瓜白粉菌的分生孢子梗基部膨大成无色的椭圆形或球形,其上逐渐产生由黄色至褐色的白粉寄生孢的分生孢子器,器内含有大量的分生孢子。  相似文献   

7.
莱氏野村菌固体发酵培养基筛选与发酵条件优化   总被引:2,自引:0,他引:2  
为探索适宜生产莱氏野村菌分生孢子的培养基及培养条件,利用单因素试验对大豆、小麦、燕麦、大米等材料进行筛选,并优化发酵条件。结果表明,不同基质对莱氏野村菌分生孢子产生、孢子活力、抗逆性和毒力有明显影响。莱氏野村菌在大豆上的产孢量和孢子活力明显高于其它三种基质,但小麦上培养的孢子抗逆性和毒力明显高于其它处理。小麦预浸泡12h后进行发酵,产孢量比对照提高25.9%;小麦浸泡后粉碎成颗粒,可显著提高产孢量;在粉碎的麦粒中添加2/5~3/5(w/w)的谷壳增加其透气性,有利于分生孢子产生,产孢量比对照提高34.7%~42.0%。固体基质接种后的初始含水量和培养温度是影响产孢的重要因素,含水量为65%、培养温度为24~26℃适宜菌体生长和分生孢子产生。光照是分生孢子产生的必需条件,连续光照有利于分生孢子产生。  相似文献   

8.
 杨树水泡型溃疡病分布广泛,严重为害杨树。分生孢子是主要的侵染源。病菌由伤口、皮孔或表皮侵入寄主。每年5~6月为春季发病高峰,9月为秋季发病高峰,秋季发病较春季为重。孢子的飞散高峰在8~9月。病害的消长与降雨量和相对湿度密切相关,雨季孢子飞散较多,分生孢子萌发的最适温度为25~30℃,子囊孢子萌发的最适温度为20~30℃。分生孢子萌发要求水分,在黑暗下发芽率高。病原可潜伏侵染,一般在2~3年生枝干上侵染较多,7~9月是潜伏侵染的高峰。除杨树外,还能为害多种阔叶树。病原在麦芽糖和蛋白胨培养基中菌丝生长较旺盛,在蔗糖和硝酸钾培养基中有利于分生孢子器形成,杨树树皮汁液能促进分生孢子发芽。  相似文献   

9.
 我国高粱上发生的新病害顶腐病是由亚粘团串珠镰孢(Fusarinm moniliforme var.subglutinans Wr.&Reink.)侵染引起的。病菌生长的适宜温度为25~30℃,适宜pH值为6~8。小型分生孢子萌发的适宜温度为25~28℃,适宜pH值为6~7。病菌在Bilai培养基上,pH4~11间均易产生大型分生孢子。黑光灯和日光灯照射对大型分生孢子形成有促进作用,且黑光灯优于日光灯;在光照处理下最适宜产生大型孢子的培养基为小麦粒和高粱粒。病菌在PSA培养基上培养10~12天后可产生厚垣孢子。病菌能利用多种碳源,以半乳糖、甘露糖为佳,乳糖、木糖、葡萄糖次之。对氮源利用远不及碳源。人工接种条件下,病菌能侵染高粱、苏丹草、哥伦布草、玉米、谷子、珍珠粟、薏苡、水稻、燕麦、小麦、狗尾草等禾本科植物。  相似文献   

10.
MB和CMC液体培养基对禾谷镰孢产孢水平的影响   总被引:1,自引:0,他引:1  
禾谷镰孢分生孢子定量接种是研究作物抗禾谷镰孢的必要手段?本试验利用绿豆(mung bean, MB)与羧甲基纤维素(carboxylmethyl cellulose, CMC)液体培养基在相同条件下培养禾谷镰孢, 比较两种培养基对禾谷镰孢产孢效率的影响; 并用两种培养基诱导分生孢子制成相同浓度孢子悬浮液, 对75个玉米家系进行人工接种鉴定, 检测不同培养基所产分生孢子致病性差异?结果表明, CMC培养基诱导分生孢子增长率(k2=1.125)大于MB培养基诱导增长率(k1=0.844)?在培养第14天, MB培养基诱导获得的分生孢子平均浓度为2.51×105个/mL, CMC培养基诱导的为3.62×105个/mL, 比MB培养基诱导多44.22%?用两种培养基诱生的孢子进行田间接种, 玉米穗腐病发病程度无明显差异?CMC培养基具有产孢快?孢子浓度高的优点, 是一种适宜禾谷镰孢分生孢子诱生的高效液体培养基?  相似文献   

11.
Symptoms of Welsh onion leaf blight, caused by Stemphylium vesicarium, are divided into two types, i.e., brown oval lesions and yellow mottle lesions. Yellow mottle lesions exert considerable economic damage on Welsh onion in northern Japan. In this study, we investigated the life cycle of the pathogen in terms of seasonal fluctuation of spore dispersal and its relationship with development of disease, formation period of pseudothecia and overwintering of the pathogen based on field surveys, spore trapping and fungal isolation. Conidia were trapped throughout the cropping season except before mid June, when no ascospores were trapped. Brown oval lesions, which contained a large number of conidia, usually occurred in July followed by yellow mottle lesions with an increasing number of conidia trapped. These observations suggest that conidia released from brown oval lesions play an important role as a secondary inoculum source of the disease, leading to the development of yellow mottle lesions. Pseudothecia on leaves were first observed at the end of the cropping season or immediately after harvest (late October). The pathogen overwintered in the form of pseudothecia produced on leaves with or without symptoms. Ascospores failed to be trap in the field during the interval between before and beginning of the cropping season in April–May. However, pot experiments demonstrated that ascospores were released from leaf debris in November and rapidly increased in number after snow melt. From this circumstantial evidence, we hypothesize that ascospores are the primary inoculum source of Welsh onion leaf blight.  相似文献   

12.
苹果炭疽叶枯病(Glomerella cingulata)是我国苹果上新发现的一种病害,为了了解病原菌的产孢条件和产孢动态,为病害的预测预报与防控提供依据。本研究在人工控制条件下,测试了温度、湿度和光照对苹果炭疽叶枯病菌产生分生孢子和子囊孢子的影响。结果表明,苹果炭疽叶枯病新形成的病叶润湿后,在15℃~30℃下保湿培养2~6 d后可产生大量橘黄色的分生孢子堆,其中30℃下产孢量最大,产孢速度最快,仅需2 d时间。炭疽叶枯病菌在新形成的病叶上于15℃~30℃下培养20~30 d可形成子囊孢子,最适温度为25℃,子囊孢子的形成需要高湿环境或叶片润湿。炭疽叶枯病菌的单孢分离菌株于15℃~25℃下,在马铃薯葡萄糖琼脂培养基(PDA)上培养20~30 d也可形成子囊孢子,最适产孢温度25℃。紫外光、黑光和日光都能促进子囊孢子的形成。  相似文献   

13.
 水稻紫鞘病是我国南方稻区生产上的一个新问题,发生面广,为害较重。经1978~1984年的研究,找到了引起紫鞘的病原茵是Acrocylindrium oryzae。带菌种子是本病的主要初次侵染来源;保存在干燥状态下的病稻草也有传病作用,稻田后期的某些虫、螨,可以传播病菌。紫鞘病病原菌的主要侵染方式是系统侵染。水稻孕穗期喷雾接菌,也能形成紫鞘,但注射法伤口接种时,大多形成虎纹斑烂鞘。因此,紫鞘是水稻叶鞘腐败病的又一种典型症状。病菌生长与产生孢子的适温为25~30℃。孕穗期接菌,其潜育期:30℃为1天,25~28℃为2天,23℃为3天,19℃为4天。  相似文献   

14.
王国良 《植物保护》2004,30(1):36-39
离体和盆栽试验表明,草莓白粉病菌经38℃高温处理8 h,分生孢子不能萌发;或每天38℃处理8 h,适温下16 h连续培养4 d后病斑不再产生分生孢子。据田间试验和调查,在浙江宁波夏季自然条件下繁育草莓苗,草莓白粉病菌不能存活到秋季,但当草莓生长良好或在有明显遮阳条件下繁育苗,少数病菌可以在草莓上越夏,越夏部位多在病株9月间仍保持绿色或部分绿色的原发病部位的匍匐茎段上。  相似文献   

15.
细辛叶枯病病原菌及其生物学研究   总被引:3,自引:0,他引:3  
 研究确认细辛叶枯病病原菌为槭菌刺孢(Mycocentrospora acerina(Hartig) Deighton),是我国真菌新记录种。该菌分生孢子萌芽和菌丝生长的最适温度为15~20℃、最适pH7。分生孢子在清水中即可萌芽,条件适宜时0.5h即可产生芽突、5h萌芽率近100%。分生孢子致死温度接近50℃。田间病残叶上的分生孢子230天后仍具9%的萌芽率。新生菌丝在有光条件下可产生鲜艳的玫瑰红色素。该菌在供试的多种培养基上不能形成分生孢子,采用菌块切割、水滴保湿的方法可以诱生大量分生孢子。该菌对细辛有较强的致病性,在人工培养条件下可以产生毒素。  相似文献   

16.
 明确黄脉爵床棒孢霉叶斑病病原菌及其生物学特性,为防控提供理论依据。通过病原菌分离、形态特征观察、致病性测定、rDNA-ITS序列分析、生物学特性及寄主范围测定等研究,证明该病病原菌为山扁豆生棒孢Corynespora cassiicola;菌丝生长及产孢适宜温度20℃~28℃,孢子萌发适宜温度24℃~32℃,菌丝致死温度49℃处理10 min;菌丝生长适宜pH 6~10,产孢适宜pH 4~8,孢子萌发最适pH 8;光暗交替适合菌丝生长与产孢,连续光照可抑制菌丝生长;菌丝生长量由少到多培养基顺序为CA、PCA、PDA、CMA、OA,而PDA上产孢最多;刺伤接种,病菌可侵染喜树(Camptotheca acuminata)等植物。黄脉爵床棒孢霉叶斑病病原为山扁豆生棒孢C. cassiicola,病菌易产孢,寄主广,潜育期短。该病菌侵染黄脉爵床为首次报道。  相似文献   

17.
王桂清  陈捷 《植物保护》2006,32(5):26-28
利用玉米灰斑病菌株20-47、感病玉米品种(掖单13)和抗病玉米品种(沈单10号),在人工气候室和自然条件下对影响玉米灰斑病菌侵染的环境条件和寄主生育期进行了研究。结果表明:玉米灰斑病是属偏高温高湿类型的病害,在温湿度条件不能得到满足时,病害就难以完成侵染发病;病菌接种侵入的最佳温度为25℃左右,水滴条件下侵染最容易;土壤条件特别是氮、磷肥如果施用不均匀、不足或过多,也都可以对结果产生影响,在通常情况下,增施氮、磷肥能提高玉米对灰斑病的抗性;在一定光照强度范围内,光对鉴定结果的影响不明显,但光暗交替更有利于寄主发病;寄主不同生育期对病原菌侵染寄主的影响不同,11~12叶期(喇叭口期)接种,病菌较易侵染。  相似文献   

18.
Apple bitter rot caused by Colletotrichum acutatum sensu lato results in fruit decay before and after harvest. We investigated the epidemiology of the disease in terms of conidial formation and dispersal as well as the change in susceptibility of fruits in Iwate, Japan. Conidia of C. acutatum were detected in rainwater collected from inside the tree canopy from May to August with peaks in production in mid-May to early June and mid- to late July. The first peak corresponded to the most conidia being produced on fruit scars, but the second peak was due to conidiation on mummified fruitlets and peduncles collected in July. Inoculation experiments revealed that fruits were susceptible to the pathogen between 20 and 90 days after petal fall and that immature fruits infected as early as 20 days after petal fall frequently developed lesions on the lower fruit half as growth progressed. These results suggest that C. acutatum sporulates on infested fruit scars to infect immature fruits, resulting in bitter rot and that the fungus also colonizes mummified fruitlets and peduncles, contributing to survival of the pathogen on fruit scars. Thus, infested fruit scars represent the primary source of inoculum.  相似文献   

19.
Experiments in controlled environments were carried out to determine the effects of temperature and leaf wetness duration on infection of oilseed rape leaves by conidia of the light leaf spot pathogen, Pyrenopeziza brassicae . Visible spore pustules developed on leaves of cv. Bristol inoculated with P. brassicae conidia at temperatures from 4 to 20°C, but not at 24°C; spore pustules developed when the leaf wetness duration after inoculation was longer than or equal to approximately 6 h at 12–20°C, 10 h at 8°C, 16 h at 6°C or 24 h at 4°C. On leaves of cvs. Capricorn or Cobra, light leaf spot symptoms developed at 8 and 16°C when the leaf wetness duration after inoculation was greater than 3 or 24 h, respectively. The latent period (the time period from inoculation to first spore pustules) of P. brassicae on cv. Bristol was, on average, approximately 10 days at 16°C when leaf wetness duration was 24 h, and increased to approximately 12 days as temperature increased to 20°C and to 26 days as temperature decreased to 4°C. At 8°C, an increase in leaf wetness duration from 10 to 72 h decreased the latent period from approximately 25 to 16 days; at 6°C, an increase in leaf wetness duration from 16 to 72 h decreased the latent period from approximately 23 to 17 days. The numbers of conidia produced were greatest at 12–16°C, and decreased as temperature decreased to 8°C or increased to 20°C. At temperatures from 8 to 20°C, an increase in leaf wetness duration from 6 to 24 h increased the production of conidia. There were linear relationships between the number of conidia produced on a leaf and the proportion of the leaf area covered by 'lesions' (both log10-transformed) at different temperatures.  相似文献   

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