一种监测棉铃虫对Bt杀虫晶体蛋白抗性的技术

研究了以诊断试剂盒监测棉铃虫对苏云金杆菌(Bt)杀虫晶体蛋白(ICP)抗性的技术。将1日龄幼虫在含诊断剂量的饲料中(每毫升饲料含Bt ICP0.01mg)取食7天,以生长至3龄以上的个体作为抗性个体的判断指标;筛选出人工饲料中防腐剂剂量的最佳值为每350毫升饲料中含丙酸2.5ml。经对多个棉铃虫不同抗性种群的验证试验,证明诊断试剂盒检测抗性个体频率较为精确且应用简便。     

二点叶螨对氧乐果、甲氰菊酯、四螨嗪及螨嗪菊酯混剂的抗药性

以兰州吐鲁沟公园金花忍冬植物上采集的二点叶螨为敏感种群,在室内盆栽菜豆苗上饲养繁殖后分别用氧乐果、甲氰菊酯、四螨嗪及螨嗪菊酯(甲氰菊酯 四螨嗪)混剂喷雾处理20代,获得二点叶螨抗氧乐果种群(抗性指数RF=35.84倍)、抗甲氰菊酯种群(RF=479.79倍)、抗四螨嗪种群(RF=67.26倍)以及抗混剂螨嗪菊酯种群(RF=26.75倍)。用生化法测定离体酶活性的结果表明,上述四个抗性种群的形成与体内羧酸酯酶、磷酸酯酶、谷胱甘肽转移酶的活力增加及乙酰胆碱酯酶的活性降低有关。4个抗性种群对常用15种供试药剂交互抗性测定结果表明,氧乐果、甲氰菊酯与联苯菊酯、三氟氯氰菊酯、水胺硫磷、久效磷、氰久合剂有交互抗性,甲氰菊酯还与螨蚧克有交互抗性;四螨嗪与三氯杀螨醇(RF=14.15倍)、齐螨素(RF=10.26倍)有交互抗性;螨嗪菊酯与双甲脒、氧乐菊酯有负交互抗性,RF值分别为0.85、0.71倍。     

朱砂叶螨对两种杀螨剂的抗性遗传力及风险评估

在室内抗性培育的基础上,应用数量遗传学中的域性状分析法研究了朱砂叶螨对甲氰菊酯和阿维菌素两种杀螨剂的抗性现实遗传力,并对两种药剂在不同杀死率下,朱砂叶螨抗性发展的速率进行了预测。结果表明,用甲氰菊酯、阿维菌素分别连续汰选16、18代后,朱砂叶螨对两者的抗性分别为28.61和4.36倍,抗性现实遗传力分别为0.2685和0.1385。在室内选择条件下,杀死率为50％～90％时,要获得10倍抗性,甲氰菊酯需要约13～6代,阿维菌素需要约28～13代。生物源农药阿维菌素的抗性风险明显低于菊酯类药剂甲氰菊酯。试验结果为朱砂叶螨抗性治理提供了理论依据。     

转基因食品的检测方法

目前，世界各国对转基因食品的检测主要从外源DNA和蛋白两种生物大分子入手，所广泛采用的方法有聚合酶链式反应（PCR）、生物芯片技术（Biochips)、酶联免疫吸附测定（ELISA）和侧流技术（Lateral Flow)。本文综述了各种方法的原理以及这些方法用于检测转基因食品时的优缺点。     

转 Bt基因抗虫棉对棉大卷叶螟抗性的研究

:转Bt基因抗虫棉对棉铃虫有很好的抗性,对棉大卷叶螟(SyleptaderogataFabricius)的抗性未见报道。作者研究表明,棉大卷叶螟在棉田为聚集分布型,低龄幼虫有集中为害习性;抗虫棉对其有很好的抗性,平均虫株率为2.2%,较常规棉中棉所12降低96.6%;百株虫量为133.8头,较常规棉降低88.4%。     

Development and fecundity ofSitobion avenae on some wheat cultivars under laboratory conditions

Nymphal development time and fecundity ofSitobion avenae (F.) (Homoptera: Aphididae) were determined on nine widespread wheat varieties cultivated in Tekirdağ Region in Turkey. Tests were carried out in controlled environment chambers (25±1°C, 65±5% r.h.; 16:8, L:D). Development time (±S.E.) ranged from 5.75±0.25 to 7.20±0.20 days. Fecundity per female ofS. avenae was found to be the highest (12.87±1.50) on wheat cv. ‘Sana’. In this investigation cvs. ‘MV-17’, ‘Miryana’, ‘Pehlivan’ and ‘Saraybosna’ were particularly resistant againstS. avenae. http://www.phytoparasitica.org posting July 8, 2002.     

Identification of ALS inhibitor‐resistant Amaranthus biotypes using polymerase chain reaction amplification of specific alleles

Summary Polymerase chain reaction (PCR) amplification of specific alleles (PASA) was adapted as a molecular marker‐based method for the rapid detection of point mutations in Amaranthus retroflexus and Amaranthus rudis leading to ALS inhibitor resistance. Two pairs of primers were designed for the specific amplification of alleles of the ALS gene of susceptible and resistant biotypes. The allele‐specific primer matched the desired allele, but mismatched the different allele at its 3′ end. Differentiation was carried out by comparison of the amplified DNA fragments in gel electrophoresis after PASA‐PCR. In A. rudis, differentiation was possible with one PCR and genomic DNA as probe. A ‘nested’ PCR was necessary for the differentiation of sensitive and resistant A. retroflexus. PASA is useful for the identification of resistant weed biotypes and also as a monitoring tool to map resistance occurrence and distribution. Advantages include the fast and clear separation of those plants with and without mutations at an early stage of development, its easy and consistent performance and quick results compared with existing resistance detection tests. These advantages, when combined with management strategies, enable further activities to reduce herbicide resistance.     

转Bt基因棉在安庆市大面积种植后害虫发生特点调查

根据调查,转Bt基因棉大面积种植后,棉铃虫、红铃虫发生减轻;棉叶螨发生加重,为害时间延长;甜菜夜蛾、斜纹夜蛾发生面积扩大,为害程度加重。据此初步提出了当地转Bt基因棉害虫防治中应注意的问题和管理对策。     

β- 氨基丁酸诱导甜( 辣) 椒抗疫病作用的研究

 报道了用β- 氨基丁酸( DL-β-aminon-butyric acid, BABA) 喷雾处理辣椒叶片和茎后的诱导抗疫病作用。研究证明: 高浓度BABA ( 1 000 g/mL) 对离体辣椒疫霉病菌无抗菌活性, 用其喷雾处理辣椒的茎叶所诱导的抗疫病作用可完全控制其危害; 用BABA 诱导处理后3 d 接种辣椒疫霉病菌, 辣椒植株开始表达出较高的诱导抗性, 这种抗病作用可持续20 d 以上, 并表现出与数量抗病性相似的特性。     

Natural tolerance of Cuscuta campestris to herbicides inhibiting amino acid biosynthesis

The response of Cuscuta campestris Yuncker, a non‐specific above‐ground holoparasite, to amino acid biosynthesis inhibitor (AABI) herbicides, was compared with other resistant and sensitive plants in dose–response assays carried out in Petri dishes. Cuscuta campestris was found to be much more resistant to all AABI herbicides tested. The I₅₀ value of C. campestris growth inhibition by glyphosate was eightfold higher than that of transgenic, glyphosate‐resistant cotton (RR‐cotton). The I₅₀ value for C. campestris shoot growth inhibition by sulfometuron was above 500 μM, whereas that of sorghum roots was only 0.004 μM. Cuscuta campestris exposed to glyphosate gradually accumulated shikimate, confirming herbicide penetration into the parasite and interaction with an active form of the target enzyme of the herbicide, 5‐enolpyruvylshikimate‐3‐phosphate synthase. More than half of the C. campestris plants associated with transgenic, glyphosate‐resistant sugarbeet (RR‐sugarbeet) treated with glyphosate or with transgenic, sulfometuron‐resistant tomato (SuR‐tomato) treated with sulfometuron recovered and resumed regular growth 20–30 days after treatment. New healthy stems developed, followed by normal flowering and seed setting. The results of the current study demonstrate the unique capacity of C. campestris to tolerate high rates of AABI. The mechanism of this phenomenon is yet to be elucidated.