防治牡丹根腐病的有效药剂筛选

采用菌丝生长速率法和孢子萌发法,分别测定了咪鲜胺、醚菌酯、苯醚甲环唑、百菌清、多菌灵、代森锰锌等6种杀菌剂对牡丹根腐病菌的室内毒力。结果表明,6种药剂对病菌菌丝生长的EC50大小顺序为：咪鲜胺<多菌灵<代森锰锌<苯醚甲环唑<百菌清<醚菌酯,其中以咪鲜胺对牡丹根腐病病菌的菌丝生长抑制作用最强, EC50为0.200 mg/L;多菌灵、代森锰锌、苯醚甲环唑、百菌清依次减弱,醚菌酯的抑制菌丝生长的作用最小,EC50为33.98 mg/L。6种药剂对病菌孢子萌发的EC50大小顺序为：百菌清<咪鲜胺<苯醚甲环唑<多菌灵<代森锰锌<醚菌酯;其中以百菌清对牡丹根腐病菌的孢子萌发抑制作用最强,EC50为0.343 mg/L;咪鲜胺、苯醚甲环唑、多菌灵、代森锰锌依次减弱,醚菌酯抑制孢子萌发的作用最小,EC50为38.4 mg/L。     

不同向日葵品种对黄萎病的抗性*

采用浸根接种法鉴定不同向日葵种质资源对黄萎病的抗性差异。结果表明：40份供试向日葵品种依据抗性划分标准共分为3类,其中中抗品种有5份如：‘118’、‘新葵杂5号’等;低抗品种有8份如‘767’、‘KJ003’等;其余27份供试材料均呈现感病;没有鉴定出免疫和高抗的向日葵品种。     

黑龙江省大豆疫霉根腐病调查与病原分离

１９９６年对黑龙江省东部和中部大豆产区２３个市、县的大豆苗期疫霉根腐病进行了调查、研究,应用ＰＢＮＩＣ疫霉选择性培养基分离大豆疫霉根腐病病原菌,从牡丹江、穆棱、林口和佳木斯豆田具疫霉根腐症状的大豆植株上分离到大豆疫霉根腐病菌,并从根腐病株上单独或与大豆疫霉菌同时分离到终极腐霉菌,研究进一步证实我国黑龙江省有大豆疫霉根腐病。调查发现,大豆疫霉根腐病和终极腐霉根腐病主要发生在土质粘重、土壤含水量高或易积水的田块。     

土壤因子对海洋多粘类芽胞杆菌L_1-9在黄瓜根表土壤定殖的影响

本试验考察了土壤温度、有机质含量和pH对海洋生防细菌多粘类芽胞杆菌L_1-9在黄瓜根表土壤中定殖的影响。采用实时荧光定量PCR方法检测了不同时期黄瓜根表土壤中菌株L_1-9的16S r DNA拷贝数。结果表明,土壤有机质含量、土壤温度和pH对菌株L_1-9在黄瓜根表的定殖有显著影响(P0.01)。25℃定殖数量最高,为5.79×108拷贝/g土,是15℃时的3.4倍;添加有机肥20~40 g/kg土壤,可以促进菌株L_1-9在黄瓜根际定殖;pH 7时,菌株L_1-9在黄瓜根表土壤中的定殖数量最高。本研究为海洋生防菌L_1-9防治黄瓜土传病害提供了理论依据。     

植物生长调节剂DTA-6对花生产量、品质及其根系生理调控研究

在大田栽培条件下,经过3年试验,研究了在花针期叶面喷施植物生长调节剂DTA-6对花生产量、品质及器官生理功能的影响。结果表明:与清水对照比较,DTA-6可显著增加荚果和籽仁产量,表现在单株干物质增加,饱荚数、饱荚重和籽仁重显著提高,秕荚数显著减少;DTA-6对籽仁中含油量具有促进作用,而对游离氨基酸、蛋白质含量有降低的趋势;同时DTA-6提高了花生的根系活力和根系伤流量以及根系的吸收和合成能力,提高了花生的结瘤性和固氮能力。     

河南省小麦根腐线虫病的发生危害及病原鉴定

为明确河南省小麦根腐线虫病的发生危害情况及其病原线虫种类,对14个县(市)45个采样点小麦根腐线虫进行了分离调查,分别通过人工接种测定其致病性和杀线剂处理研究其危害性,并采用形态学和分子生物学方法鉴定其病原。结果显示:小麦根腐线虫在河南省的分布具有一定的区域性,中北部的10个县(市)34个沙质土壤采样点均分离出小麦根腐线虫,而在南部土壤粘重地区的小麦根内和土壤中均没有分离出根腐线虫;15%涕灭威颗粒剂处理土壤后小麦的穗粒数、千粒重和单位面积产量较对照明显上升,产量增加13.6%;该线虫能够侵染小麦,并明显抑制小麦生长;河南省小麦根腐线虫以敏捷短体线虫Pratylenchus agilis为主。     

Use of real-time PCR to examine the relationship between disease severity in pea and <Emphasis Type="Italic">Aphanomyces euteiches</Emphasis> DNA content in roots

Aphanomyces euteiches causes severe root rot of peas. Resistance is limited in commercial pea cultivars. Real-time fluorescent PCR assay specific for A. euteiches was used to study the relationship between disease severity and pathogen DNA content in infected peas. Five pea genotypes ranging in levels of resistance were inoculated with five isolates of A. euteiches. Plants were visually rated for disease development and the amount of pathogen DNA in roots was determined using the PCR assay. The susceptible genotypes Genie, DSP and Bolero tended to have significantly more disease and more pathogen DNA than the resistant genotypes 90-2079 and PI 180693. PI 180693 consistently had less disease, while 90-2079 had the lowest amount of pathogen DNA. The Spearman correlation between pathogen DNA quantity and disease development was positive and significant (P < 0.05) for three isolates, but was not significant for two other isolates. This suggests that the real-time PCR assay may have limited application as a selection tool for resistance in pea to A. euteiches. Its utility as a selection tool would be dependent on the correlation between disease development and pathogen DNA content for a given pathogen isolate. The accuracy and specificity of the real-time PCR assay suggests considerable application for the assay in the study of mechanisms of disease resistance and the study of microbial population dynamics in plants.