2017—2019年江西省二化螟种群对四种杀虫剂的抗性

为明确近年来江西省二化螟种群对常用杀虫剂的抗性水平,提出合理化用药建议,本研究采用人工饲料浸药法测定2017—2019年江西省13个县(市)二化螟田间种群对氯虫苯甲酰胺、阿维菌素、三唑磷和杀虫单的抗性。结果表明,13个二化螟种群对氯虫苯甲酰胺的抗性水平整体为中等至高水平抗性,其中有11个二化螟种群对氯虫苯甲酰胺的抗性水平整体为上升趋势,在对氯虫苯甲酰胺抗性水平增加的种群中,都昌种群的抗性倍数从2017年的44.1倍上升至2018年的65.1倍,在2019年激增至高水平抗性,抗性倍数为283.5倍,为供试种群的最高抗性倍数。13个二化螟种群对阿维菌素的抗性水平整体为中等偏下,在对阿维菌素抗性水平增加的种群中,南昌种群的抗性倍数最高,2017—2019年分别为74.8倍、108.7倍和80.6倍。13个二化螟种群对三唑磷的抗性水平整体为中等偏下,其中新干、永修、万安、大余、上高和都昌这6个种群对三唑磷的抗性水平呈波动上升的趋势,而其他7个种群对三唑磷的抗性水平为波动性变化,偶有下降。13个二化螟种群对杀虫单的抗性水平整体为中等偏下并且有明显下降趋势,其中大余、永修、泰和、会昌、新干和上高这...     

2002年江苏省二化螟抗药性检测及治理

20 0 2年应用点滴法普查了江苏常熟、锡山、武进、句容、姜堰、高邮、楚州、宿豫、灌云及连云港 10县 (市 ) 12个二化螟种群 4龄幼虫对 4种 (类 )杀虫剂的抗药性。结果表明 ,供试种群对沙蚕毒素类农药杀虫单已普遍产生抗性 ,且苏南种群的抗性水平高于苏北 ,常熟为最高 ( 16倍 ) ;对有机磷类农药三唑磷苏南地区种群为低水平抗性 ,其他地区均属敏感水平。目前二化螟供试种群对苯基吡唑类农药氟虫腈和抗生素类农药阿维菌素未产生抗药性。本文还对二化螟抗性治理对策进行了讨论。     

二化螟对不同药剂的敏感度研究

为了解江西省不同地区二化螟对不同类型杀虫剂的敏感度水平,科学指导二化螟的田间药剂防治,应用点滴法测定了江西省代表性稻区二化螟对5大类8种杀虫剂的敏感度。结果表明,靖安、南昌、吉安稻区二化螟对三唑磷、毒死蜱、稻丰散和杀虫单敏感度极低,对丁烯氟虫腈和氯虫苯甲酰胺敏感度较高,对甲维盐和阿维菌素敏感度最高;3个稻区的二化螟种群对试验药剂的敏感度,除毒死蜱和阿维菌素外（相对敏感性指数为3.88、3.85）,对其他药剂的敏感度差异不大（相对敏感性指数均低于1.5）。     

褐飞虱对氟啶虫胺腈的抗性监测与生化抗性机制

为明确我国褐飞虱田间种群对氟啶虫胺腈的抗性现状及生化抗性机制,2017年-2019年采用稻茎浸渍法测定了采集自7省共13个褐飞虱田间种群对氟啶虫胺腈的抗性,并研究了氟啶虫胺腈抗性种群与其他杀虫剂的交互抗性以及增效剂对氟啶虫胺腈的增效效果。结果表明：近3年来褐飞虱对氟啶虫胺腈产生了中等水平抗性(RR=10.3～30.9)。氟啶虫胺腈抗性品系对呋虫胺、噻虫嗪和烯啶虫胺分别产生了9.1倍、7.9倍和4.1倍的低水平交互抗性,与噻嗪酮、毒死蜱、吡蚜酮、三氟苯嘧啶和吡虫啉不存在交互抗性。增效剂PBO对氟啶虫胺腈抗性品系和浙江龙游19(Longyou-19)田间种群分别具有4.2倍和3.8倍的明显增效作用。综上,褐飞虱田间种群已对氟啶虫胺腈产生中等水平抗性。多功能氧化酶参与了褐飞虱对氟啶虫胺腈的代谢抗性。     

江西省部分地区水稻二化螟抗药性测定

用点滴法普查了江西省南昌、南城、永新、丰城、上饶、彭泽6县(市)二化螟种群4铃幼虫对4种(类)杀虫剂的抗药性。结果表明,供试二化螟种群对沙蚕毒素类农药杀虫单、有机磷类农药三唑磷已产生了较强的抗性,抗性倍数分别为33.30~241.95、7.97~111.20;对苯基吡唑类农药氟虫腈和抗生素类农药阿维茵素部分地区也产生了低水平抗性,抗性倍数分别为5.88~16.47、3.70~9.90。本文还对二化螟抗性治理对策进行了讨论。     

安徽沿江稻区二化螟抗药性动态及治理对策

二化螟是水稻上的重要害虫之一,明确其对杀虫剂的抗性是合理制定化学防治策略的依据.笔者通过2001～2009年安徽和县地区二化螟对杀虫单、三唑磷、氟虫腈和阿维菌素等4种主要药剂抗性的系统监测,分析了抗性发展动态,并在此基础上提出了安徽沿江稻区二化螟的治理对策.     

灰飞虱对几种杀虫剂的抗性

采用稻苗浸渍法测定了灰飞虱对7种常用杀虫剂的抗性。2011年监测了我国江苏、浙江、安徽三省9个灰飞虱种群对噻虫嗪、烯啶虫胺、毒死蜱、吡蚜酮、噻嗪酮、高效氯氰菊酯及氟虫腈的抗性。结果表明:灰飞虱对噻虫嗪都处于敏感阶段(0.6~2.2倍);对烯啶虫胺处于敏感阶段(0.8~3.0倍);对毒死蜱产生了中-高水平抗性(17.5~83.6倍);对吡蚜酮为敏感到低水平抗性(1.9~5.5倍);对噻嗪酮的抗性为高-极高水平(136.4~271.1倍);对高效氯氰菊酯的抗性为低-中等水平(5.2~34.9倍);对氟虫腈为低水平抗性(0.9~8.0倍)。基于灰飞虱对7种药剂的抗性情况,对田间治理灰飞虱合理使用药剂进行了讨论。     

几种药剂防治二化螟田间药效试验

近年来,二化螟已成为为害钟山县水稻主要的钻蛀性螟虫.该县用于防治二化螟的主要农药有三唑磷、毒死蜱和杀虫单等,已使用多年,防效已明显下降.据何月平等人报道:在桂林地区,二化螟对三唑磷已经达到了高水平抗性,对杀虫单和毒死蜱已经达到了中等水平抗性[1].     

陕西关中地区小麦田禾谷缢管蚜对7种杀虫剂的抗性监测

为明确陕西关中地区麦蚜田间种群对杀虫剂的抗药性现状,采用浸叶法测定了兴平、礼泉、凤翔、岐山、扶风地区麦田禾谷缢管蚜种群对高效氯氰菊酯、溴氰菊酯、吡虫啉、异丙威、毒死蜱、阿维菌素、氟啶虫胺腈等7种杀虫剂的抗性水平。结果表明,禾谷缢管蚜对高效氯氰菊酯的抗性水平最高,其中凤翔种群对高效氯氰菊酯达到高水平抗性(抗性倍数为72.5),岐山和扶风种群对该药产生中等水平抗性(抗性倍数分别为31.4、29.9);5个地区的禾谷缢管蚜对溴氰菊酯、吡虫啉、毒死蜱、异丙威和阿维菌素的抗性水平较低,表现为敏感、敏感性下降或者低抗性;5个地区的试虫对氟啶虫胺腈均表现为敏感。分析认为,高效氯氰菊酯不适合用于关中地区禾谷缢管蚜防治,氟啶虫胺腈作为一种新型杀虫剂,可以在该虫防治中推广使用,吡虫啉、阿维菌素等其他几种杀虫剂可以在禾谷缢管蚜的防治中交替使用。     

不同地区小菜蛾对杀虫剂的抗性差异

室内用浸渍法测定了 14种杀虫剂对山东泰安和浙江杭州两地小菜蛾种群的毒力。结果表明 ,两地小菜蛾对溴氰菊酯产生了高水平抗性 ,分别达 6 3.9和 52 .5倍 ;对氟啶脲的抗性也分别达 35.0和 12 2 .1倍 ;常用的有机磷类、灭多威和杀虫双等药剂对它们的毒力均较低 ;两个小菜蛾种群对阿维菌素和氟虫腈最敏感。     

Variation and Heritability of Phenology in the Fungus Monilinia vaccinii-corymbosi on Blueberry

ABSTRACT The germination of field-collected pseudosclerotia and the development of apothecia from eight New Jersey populations of the mummy berry fungus Monilinia vaccinii-corymbosi were evaluated under controlled conditions in the greenhouse. Development data for apothecia were used to describe the timing of apothecium formation and to estimate broad- and narrow-sense heritabilities of fungal phenology. Mean development times for the formation of apothecia ranged from 35.4 to 54.7 days. The mean development times for populations collected from early-season cv. Weymouth ranged from 35.4 to 39.6 days and were significantly shorter than the development times for three of the four populations collected from late-season cv. Jersey (46.9 to 54.7 days) or for the population collected from mixed stands of cultivated blueberries (42.7 days). The development of populations from late cultivars planted in very close proximity to early cv. Weymouth was early (36.5 to 39.0 days) and not significantly different from the development of populations collected from cv. Weymouth. Phenotypic and genetic variances of apothecium development for individual populations ranged from 18.9 to 44.8 and 7.2 to 30.9, respectively. Broad-sense heritabilities of apothecia development for each fungal population, calculated by partitioning phenotypic variation into genetic and environmental components, ranged from 0.31 to 0.78. Narrow-sense heritabilities of apothecia development, based on parent-offspring regression, ranged from 0.58 to 0.78. These results indicate that populations of M. vaccinii-corymbosi differ in phenology and that a significant portion of the phenological variation within populations is genetic. Thus, it is plausible to propose that the phenology of apothecium development is a component of fungal fitness and that host phenology can influence the timing of pathogen development.     

Geographic variability in response to azinphos‐methyl in field‐collected populations of Cydia pomonella (Lepidoptera: Tortricidae) from Argentina

BACKGROUND: Resistance to insecticides has been related to application history, genetic factors of the pest and the dynamic within the treated area. The aim of this study was to assess the geographic variation in azinphos‐methyl response and the role of esterase and cytochrome P450 monooxygenase enzymes in codling moth populations collected within different areas of the Río Negro and Neuquén Valley, Argentina. RESULTS: Diapausing field‐collected populations showed resistance ratios at the LC₅₀ that were 0.7–8.7 times higher than that of the susceptible strain. Mean esterase (EST) and cytochrome P450 monooxygenase activities (expressed as α‐N min^?1 mg^?1 prot^?1 and pg 7‐OHC insect^?1 min^?1 respectively) were significantly correlated with LD₅₀ values from the field‐collected populations. In addition, azinphos‐methyl response was associated with the geographic area where the insect population was collected: populations from isolated and more recent productive areas presented significantly lower resistance ratios in comparison with populations from older and more intensive productive areas. CONCLUSION: The populations assayed presented different resistance levels to azinphos‐methyl. The response was highly correlated with the orchard's geographic location. EST and ECOD activities were involved in azinphos‐methyl response in the given region. Copyright © 2012 Society of Chemical Industry     

小菜蛾种群抗性分子遗传与进化分析

小菜蛾 Plutella xylostella( L.)抗药性问题日益严重 ,对其抗性机理和治理策略的研究也较为广泛 ,但用淀粉电泳的试验方法从群体遗传学的角度研究小菜蛾的抗性发生、发展及进化规律的报道 ,国内尚不多见。为此作者用淀粉电泳结合 Genepop ( V 3.1 6 )软件同时分析了小菜蛾群体中酯酶 ( EST)、6 -磷酸葡萄糖脱氢酶 ( GPT)、苹果酸脱氢酶 ( MDH)和苹果酸酶 ( ME)的特征 ,旨在为抗性治理提供理论依据。1　材料与方法1 .1　供试小菜蛾及药品北京种群由中国农科院植保所吴奎华教授惠赠 ,采自北京郊区菜地 ;武汉、河北和云南种群由中国农业…     

Biochemical determination of acetylcholinesterase genotypes conferring resistance to the organophosphate insecticide chlorpyriphos in field populations of Bemisia tabaci from Benin, West Africa

Resistance to chlorpyriphos insecticide in Bemisia tabaci from a field population collected in Benin, West Africa was suggested with bioassay showing the presence of two sub-populations. Patterns of acetylcholinesterase (AChE) inhibition by the organophosphate chlorpyriphos-oxon were analyzed to estimate the number of possible genotypes with different sensitivity expected in three B. tabaci field populations collected in Benin. The analysis of inhibition patterns in these populations compared with four laboratory strains of B. tabaci using chlorpyriphos-oxon allowed the differentiation of three possible genotypes. In the reference strain SUD-S we detected two different acetylcholinesterases with different sensitivity to chlorpyriphos oxon suggesting the presence of two genes ace 1 and ace 2. The proportion of the insensitive enzyme (ace 2) was estimated to be 31%. In field populations we can detect two alleles at the same gene locus ace 1: one susceptible ace1S and one resistant ace1R. Both strains called Arizona University and Mexico-S2 have lost sensitive ace1S but the field populations from Benin clearly contained at least three genotypes confirming heterogeneous populations not completely resistant.     

甘薯茎腐病菌的遗传多样性及致病力差异分析

为了解不同地区甘薯茎腐病菌Dickeya dadantii种群遗传多样性水平及致病力差异,采用重复序列PCR基因指纹(repetitive element palindromic PCR,REP-PCR)技术和薯片接种方法,对采自广东省、广西壮族自治区和重庆市的6个市区县的59株菌株进行分析。结果表明,5对引物对59株菌株扩增出41个清晰的条带,其中36个为多态性条带,每对引物的扩增条带数在4～10之间,平均为7.2。在物种水平上,有效等位基因数、Nei’s基因多样性指数和Shannon信息指数分别为1.4768、0.2801和0.4186,其中湛江种群多样性最高,南宁种群多样性最低;当遗传相似系数为0.79时,59株菌株可被划分为5个类群,类群划分与菌株来源地间有一定的相关性。此外,不同地区病菌种群间存在明显的致病力差异,其中合浦种群与湛江种群致病力最强,万州种群致病力较弱。表明甘薯茎腐病菌种群具有丰富的遗传多样性,不同地区的病菌种群存在明显的遗传多样性与致病力差异。     

Genetic diversity and population structure of Striga hermonthica populations from Kenya and Nigeria

Striga hermonthica is a parasitic weed that poses a serious threat to the production of economically important cereals in sub‐Saharan Africa. The existence of genetic diversity within and between S. hermonthica populations presents a challenge to the successful development and deployment of effective control technologies against this parasitic weed. Understanding the extent of diversity between S. hermonthica populations will facilitate the design and deployment of effective control technologies against the parasite. In the present study, S. hermonthica plants collected from different locations and host crops in Kenya and Nigeria were genotyped using single nucleotide polymorphisms. Statistically significant genetic differentiation (F_ST = 0.15, P = 0.001) was uncovered between populations collected from the two countries. Also, the populations collected in Nigeria formed three distinct subgroups. Unique loci undergoing selection were observed between the Kenyan and Nigerian populations and among the three subgroups found in Nigeria. Striga hermonthica populations parasitising rice in Kenya appeared to be genetically distinct from those parasitising maize and sorghum. The presence of distinct populations in East and West Africa and in different regions in Nigeria highlights the importance of developing and testing Striga control technologies in multiple locations, including locations representing the geographic regions in Nigeria where genetically distinct subpopulations of the parasite were found. Efforts should also be made to develop relevant control technologies for areas infested with ‘rice‐specific’ Striga spp. populations in Kenya.     

不同种群螟黄赤眼蜂和松毛虫赤眼蜂的抗药性测定

分别测定了螟黄赤眼蜂和松毛虫赤眼蜂各5个不同地理种群对灭多威、溴氰菊酯、辛硫磷的室内抗性水平。结果表明,不同地区或不同生态条件下的赤眼蜂种群具有抗药性差异。螟黄赤眼蜂的敏感种群为采自吉林省长春市的农场种群,与之比较,其他4个种群对灭多威的LC50的变化范围为其1.93～6.72倍,对溴氰菊酯的LC50为其5.35～39.08倍,对辛硫磷的LC50为其3.49～29.76倍;松毛虫赤眼蜂的敏感种群为采自黑龙江省尚志市的亚布力南种群,与之比较,其他各个种群对灭多威的LC50的变化范围为其9.52～70.66倍,对溴氰菊酯的LC50为其73.12～288.16倍,对辛硫磷的LC50的变化范围为11.84～50.38倍。     

Genetic Diversity and Structure of the Apiosporina morbosa Populations on Prunus spp

ABSTRACT Populations of Apiosporina morbosa collected from 15 geographic locations in Canada and the United States and three host species, Prunus virginiana, P. pensylvanica, and P. padus, were evaluated using the sequence-related amplified polymorphism (SRAP) technique to determine their genetic diversity and population differentiation. Extensive diversity was detected in the A. morbosa populations, including 134 isolates from Canada and the United States, regardless of the origin of the population. The number of polymorphic loci varied from 6.9 to 82.8% in the geographic populations, and from 41.4 to 79.3% in the populations from four host genotypes based on 58 polymorphic fragments. In all, 44 to 100% of isolates in the geographic populations and 43.6 to 76.2% in populations from four host genotypes represented unique genotypes. Values of heterozygosity (H) varied from 2.8 to 28.3% in the geographic populations and 10.2 to 26.1% in the populations from four host genotypes. In general, the A. morbosa populations sampled from wild chokecherry showed a higher genetic diversity than those populations collected from other host species, whereas the populations isolated from cultivated chokecherry, P. virginiana 'Shubert Select', showed a reduction of genetic diversity compared with populations from wild P. virginiana. Significant population differentiation was found among both the geographic populations (P < 0.05) and populations from different host genotypes (P < 0.02). In the geographic populations, most of populations from cultivated and wild P. virginiana were closely clustered, and no population differentiation was detected except for the populations from Morris, Morden, and Winnipeg, Manitoba, Canada. Furthermore, the populations from P. virginiana in the same geographic locations had higher genetic identity and closer genetic distance to each other compared with those from different locations. Four populations from P. virginiana, P. pensylvanica, and P. padus, were significantly differentiated from each other (P < 0.02), except there was no differentiation between the Shubert Select and wild chokecherry populations (>P> = 0.334). Indirect estimation of gene flow showed that significant restricted gene flow existed between populations from different regions and host species. Gene flow rates (Nm) varied from <1 to 12.5, with higher gene flow rates among population pairs from the same host species (P = 1.000). The analysis of molecular variance revealed that a major genetic variance source came from the genetic variation among isolates within populations regardless of the origin and host genotype of the population. Although some locations had a limited number of isolates, the results of this study clearly showed that the genetic diversity and population differentiation of A. morbosa were closely associated with host genotypes and geographic locations, but mostly with the former.     

Occurrence of virulent root-knot nematode populations on tomatoes bearing the <Emphasis Type="Italic">Mi</Emphasis> gene in protected vegetable-growing areas of Turkey

Root-knot nematodes (Meloidogyne spp.; RKN) are one of the most important pathogens of vegetables in Turkey. Assessing the existing virulent RKN populations is of importance for pathogen mapping in the west Mediterranean region of Turkey. Therefore, 95 populations of RKN were collected from different protected vegetable-growing locations in the region. Pure cultures were obtained and identified by means of species-specific primers. Virulence of the populations against the Mi-1 gene conferring resistance to Meloidogyne incognita, M. javanica and M. arenaria was determined according to their egg masses and gall rating on resistant and susceptible tomato varieties. Results showed that seven populations of M. incognita and six populations of M. javanica were able to overcome the resistance controlled by the Mi-1 gene. The frequency of virulent populations of M. incognita and M. javanica collected from different protected-grown vegetables was 11.7% and 21.4%, respectively. To our knowledge, this is the first report of populations of RKN virulent to the Mi-1 gene in Turkey.     

The Genetic Structure of Australian Populations of Mycosphaerella musicola Suggests Restricted Gene Flow at the Continental Scale

ABSTRACT Mycosphaerella musicola causes Sigatoka disease of banana and is endemic to Australia. The population genetic structure of M. musicola in Australia was examined by applying single-copy restriction fragment length polymorphism probes to hierarchically sampled populations collected along the Australian east coast. The 363 isolates studied were from 16 plantations at 12 sites in four different regions, and comprised 11 populations. These populations displayed moderate levels of gene diversity (H = 0.142 to 0.369) and similar levels of genotypic richness and evenness. Populations were dominated by unique genotypes, but isolates sharing the same genotype (putative clones) were detected. Genotype distribution was highly localized within each population, and the majority of putative clones were detected for isolates sampled from different sporodochia in the same lesion or different lesions on a plant. Multilocus gametic disequilibrium tests provided further evidence of a degree of clonality within the populations at the plant scale. A complex pattern of population differentiation was detected for M. musicola in Australia. Populations sampled from plantations outside the two major production areas were genetically very different to all other populations. Differentiation was much lower between populations of the two major production areas, despite their geographic separation of over 1,000 km. These results suggest low gene flow at the continental scale due to limited spore dispersal and the movement of infected plant material.