氨基甲酸酯杀虫剂灭蚜威及其与阿维菌素的混配制剂对美洲斑潜蝇的防治效果

田间试验表明 ,氨基甲酸酯新杀虫剂灭蚜威单剂与生物农药阿维菌素混剂对美洲斑潜蝇Liro myzasativae防治效果优良。 5 0 %灭蚜威可湿粉使用剂量 2 5g(a .i.) 667m2 的 3～ 1 1d校正防效为85 2 8%～ 86 3 9% ,1 8 75g(a.i.) 667m2 相应药效为 83 0 1 %～ 84 0 4%。 3种不同配比的灭蚜威与阿维菌素混剂使用剂量 1 0g(a .i.) 667m2 ,药后 3～ 1 1d防效为 85 90 %～ 90 3 3 % ,7 5g(a .i.) 667m2 相应药效为 83 48%～ 88 5 2 %。     

有机磷类杀虫剂对美洲斑潜蝇的防治效果

在山东青州以西葫芦为试验害虫寄主 ,测定了毒死蜱、三唑磷、乙酰甲胺磷、辛硫磷、马拉硫磷对美洲斑潜蝇幼虫LiriomyzasativaeBlanchard的田间防效。毒死蜱 (2 4g (a .i.) 667m2 )、三唑磷 (1 0g (a.i.) 667m2 )、乙酰甲胺磷 (2 0g (a .i.) 667m2 )第 3～ 7d校正防效为 97 0 9%～ 97 1 4% ,86 80 %～87 0 4% ,85 99%～ 86 2 5 %。此 6个处理药效顺序为毒死蜱 >三唑磷 >乙酰甲胺磷 (2 0g(a.i.) 667m2 )>乙酰甲胺磷 (1 5g(a.i.) 667m2 ) >辛硫磷 >马拉硫磷。在河南洛阳以甘蓝为试验害虫寄主 ,乙酰甲胺磷 (1 5g(a.i.) 667m2 )、敌敌畏 (2 5g(a.i.) 667m2 )、敌百虫 (4 5g(a .i.) 667m2 )对美洲斑潜蝇幼虫第 7d校正防效分别为 76 98% ,82 42 % ,71 1 1 %。毒死蜱对在不同寄主上美洲斑潜蝇的防效均较好     

氨基甲酸酯类杀虫剂灭蚜威对麦蚜的防治效果

田间试验表明 :氨基甲酸酯新杀虫剂灭蚜威是一种对麦蚜杀虫活性高的杀虫剂 ,2 5 %灭蚜威EC使用剂量 9 375～ 1 2 5g (a .i.) 667m2 ,药后 3～ 1 0d校正防效山东河南两地分别为 87 64%～ 98 38%和 89 95 %～ 97 66% ,6 2 5g (a .i.) 667m2 药后 7～ 1 0d防效分别为 87 68%～ 92 0 2 %和 88 91 %～94 4 6% ;5 0 %灭蚜威WP使用剂量 1 8 75～ 2 5g (a.i.) 667m2 ,药后 3～ 1 0d防效两地分别为 89 1 7%～99 4 5 %和 93 60 %～ 99 2 3% ,1 2 5g (a.i.) 667m2 药后 7～ 1 0d防效分别为 90 60 %～ 93 5 9%和 92 37%～ 93 5 0 %。     

阿维菌素、伊维菌素和芽孢杆菌对美洲斑潜蝇的防治效果

田间试验结果表明 ,阿维菌素对美洲斑潜Liriomyzasativae蝇幼虫防效较好 ,优于伊维菌素对美洲斑潜蝇的防效 ,可较好地控制美洲斑潜蝇幼虫的危害 ,而Btg,Bti,Bs不宜单独用于防治美洲斑潜蝇幼虫。阿维菌素用量为 0 2 7,0 3 6,0 45g (a .i.) 667m2 时 ,对美洲斑潜蝇幼虫防效第 7d校正防效为 65 %左右 ,施药后第 1 1d校正防效为 85 48%～ 99 0 5 % ,施药后第 1 5d校正防效为 90 94%～ 99 89%。伊维菌素 0 5g (a .i.) 667m2 施药后第 3 ,7,1 1d校正防效分别为 61 67% ,90 5 3 % ,90 93 % ,伊维菌素 0 2 5g(a i ) 667m2 相应防效为 5 7.71 % ,84 68% ,85 83 %。Btg ,Bti,Bs施药后第 3 ,7,1 1d校正防效为 3 3 88%～ 5 5 5 4%。     

甲氰菊酯与阿维菌素的混剂防治美洲斑潜蝇田间试验

田间试验表明 ,1 9%甲氰·阿维EC 9 5g (a .i.) 667m2 对美洲斑潜蝇LiriomyzasativaeBlanchard的校正防效药后 3～ 1 1d为 87 2 2 %～ 91 3 2 % ;7 1 2 5g (a.i.) 667m2 药后 3～ 1 1d为 81 2 9%～ 85 1 0 % ;9 5g (a .i.) 667m2 药后 3～ 1 1d防效显著优于单剂甲氰菊酯 ,药后 3～ 7d显著优于单剂阿维菌素 ,药后11d防效与阿维菌素无显著区别。 1 5 %甲氰·阿维EC 7 5g (a .i.) 667m2 对美洲斑潜蝇的校正防效药后3～ 1 1d为 85 5 9%～ 89 0 9% ;5 62 5g (a .i.) 667m2 药后 3～ 1 1d为 77 1 5 %～ 85 95 %。 1 0 %甲氰·阿维EC 7 5g (a .i.) 667m2 对美洲斑潜蝇的校正防效药后 3～ 1 1d为 85 5 9%～ 89 0 9% ;5 62 5g (a .i.) 667m2 药后 3～ 1 1d为 77 1 5 %～ 85 95 %。混剂的药效基本随有效成分含量的提高而提高。     

杀虫威对棉铃虫、烟青虫、菜青虫的防治效果

田间试验表明 ,新氨基甲酸酯杀虫剂杀虫威对鳞翅目害虫棉铃虫、菜青虫、烟青虫防治效果优良。杀虫威 2 0 %EC在河南防治 2代棉铃虫使用剂量 1 0g (a.i.) 667m2 药后 2～ 7d ,校正防效为90 65 %～ 97 72 % ,在山东药后 3～ 5d ,防效为 85 1 7%～ 91 2 3 % ,7 5g (a .i.) 667m2 相应药效两地分别为 88 41 %～ 95 2 7%和 81 40 %～ 85 61 % ;防治 3代棉铃虫使用剂量 2 0g (a.i.) 667m2 药后 2～ 5d ,防效两地分别为 83 93 %～ 86 1 5 %和 85 5 3 %～ 88 2 9% ,1 5g (a .i.) 667m2 相应药效分别为 77 66%～80 2 3 %和 78 5 0 %～ 83 75 %。防治烟青虫使用剂量 1 0g (a.i.) 667m2 药后 3～ 7d校正防效为 85 5 7%～ 88 2 9% ,7 5g (a .i.) 667m2 相应药效为 81 5 1 %～ 86 1 1 %。防治菜青虫使用剂量 7 5～ 1 0g (a .i.) 667m2 药后 3～ 7d防效为 87 5 0 %～ 96 1 1 %。     

氯氟氰菊酯与阿维菌素增效混配制剂对美洲斑潜蝇的防治效果

低毒化学杀虫剂氯氟氰菊酯与生物源农药阿维菌素混配,通过其对美洲斑潜蝇室内毒力实验,测定共毒系数CTC为161～232,处于明显增效范围内。据此确定最佳配比,配制此增效混剂2%渗透型可湿性粉剂。在北京、山东两地防治美洲斑潜蝇幼虫的田间试验表明药效优良,制剂用量50 g/667m²药后3、7、11天两地区校正防效分别为85.26%～90.76%和86.74%～94.02%,制剂用量25g/667m2两地区相应防效分别为75.28%～85.17%、79.96%～88.68%。该增效混剂防治斑潜蝇速效性和持效性皆佳,成本有所下降,使用可湿粉与乳油相比较,可减少投放入环境的化学品数量,以减少环境污染。     

毒死蜱与阿维菌素增效混配制剂对斑潜蝇属害虫的防治效果

通过有机磷杀虫剂毒死蜱与生物源农药阿维菌素混配制剂对美洲斑潜蝇Liriomyza sativae室内毒力实验,测定共毒系数为165～234,处于明显增效范围内。据此确定最佳配比和次佳配比,配制该增效混剂30%渗透型可湿性粉剂-1和-02,在山东防治美洲斑潜蝇幼虫的田间试验表明药效优良。制剂用量50 g/667m²药后3,7,11天,两可湿粉的校正防效分别为90.43%～91.71%和87.09%～90.53%,可湿粉-1用量25 g/667m²防效为85.96%～88.28%,可湿粉-2用量37.5 g/667m²相应校正防效为84.01%～85.38%,两增效混剂防治斑潜蝇速效性和持效性皆佳,成本有所下降,且对南美洲斑潜蝇L. huidobrensis亦有较好防效。使用可湿粉与乳油相比较可减少投放入环境的化学品数量。     

三种杀虫剂对麦田蚜虫和天敌的影响

通过对施用杀虫剂吡虫啉、抗蚜威、广谱性杀虫剂氧化乐果对麦田蚜虫和天敌的影响进行分析 ,结果表明 ,施用杀虫剂对麦田蚜虫防效高 ,对其天敌有保护作用 ,且瓢蚜比降低。使用 1 0 %吡虫啉( 1 0g 667m2 )后 5～ 2 5天瓢蚜比为 1∶34～ 1∶1 70 ;用 50 %抗蚜威 ( 5g 667m2 )后 1 0～ 2 0天瓢蚜比为 1∶31～1∶1 95;而广谱性杀虫剂氧化乐果 ( 50mL 667m2 )对麦田蚜虫防效好 ,对天敌杀伤力大 ,药后 1 5天瓢蚜比为1∶2 65。施用化学农药可使蚜茧蜂寄生率提高。     

0.4%根施净颗粒剂防治烟蚜田间药效和减轻烟草病毒病的试验

在烟苗移裁期应用0.4％根施净颗粒剂根区施药防治烟蚜进行了试验,试验表明,应用1—3kg／667m。施药后59天和82天防蚜效果分别为97．4—99．8和79．3—88．5％,不同用药量间差别不大,同期内使用5％涕灭威颗粒剂(1kg／667m。)防治烟蚜效果仅为44．1和15．4％,从防蚜效果和经济考虑建议使用1kg／667m。药量为宜,调查表明：在早期防治蚜虫也明显地减轻烟草病毒病的发生。     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen derAlismataceae,Liliaceae, Juncaceae,Cyperaceae, Poaceae undAraceae

Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.

     

Identification and Characterization of the First Equine Parainfluenza Virus 5

正Dear Editor,Parainfluenza virus 5 (PIV5), known as canine parainfluenza virus in the veterinary field, is a negative-sense,nonsegmented, single-stranded RNA virus belonging to the Paramyxoviridae family (Chen 2018). The virus was first reported in primary monkey kidney cells in 1954 (Hsiung1972), then it has been frequently discovered in various     

Pathogenic Characterization and Full Length Genome Sequence of a Reassortant Infectious Bursal Disease Virus Newly Isolated in Pakistan

<正>Dear Editor,Infectious bursal disease (IBD) is one of the most important diseases of the poultry. The IBD virus (IBDV), a nonenveloped virus belonging to the Birnaviridae family with a genome consisting of two segments of double-stranded RNA (segments A and B), targets B lymphocytes of bursa of Fabricious leading to immunosuppression. In Pakistan,poultry farming is the second biggest industry and IBD is the second biggest disease threating the poultry sector.However, there is limited genome information of IBDV     

Mink Circovirus Can Infect Minks,Foxes and Raccoon Dogs

正Dear Editor,Mink circovirus (MiCV), which is clustered in the genus Circovirus of the family Circoviridae, was first described in minks from farms in Dalian, China in 2013 (Lian et al.2014). The complete single-stranded circular genome of the virus is 1,753 nucleotides long and contains two major open reading frames (ORFs), designated ORF1 (Rep gene)and ORF2 (Cap gene)(Lian et al. 2014; Ge et al. 2018).Sequence analysis has shown that MiCV is most closely     

CypA Regulates AIP4-Mediated M1 Ubiquitination of Influenza A Virus

Cyclophilin A (CypA) is a peptidyl-prolyl cis/trans isomerase that interacts with the matrix protein (M1) of influenza A virus (IAV) and restricts virus replication by regulating the ubiquitin–proteasome-mediated degradation of M1. However,the mechanism by which CypA regulates M1 ubiquitination remains unknown. In this study, we reported that E3 ubiquitin ligase AIP4 promoted K48-linked ubiquitination of M1 at K102 and K104, and accelerated ubiquitin–proteasome-mediated degradation of M1. The recombinant IAV with mutant M1 (K102 R/K104 R) could not be rescued, suggesting that the ubiquitination of M1 at K102/K104 was essential for IAV replication. Furthermore, CypA inhibited AIP4-mediated M1 ubiquitination by impairing the interaction between AIP4 and M1. More importantly, both the mutations of M1 (K102 R/K104 R) and CypA inhibited the nuclear export of M1, indicating that CypA regulates the cellular localization of M1 via inhibition of AIP4-mediated M1 ubiquitination at K102 and K104, which results in the reduced replication of IAV.Collectively, our findings reveal a novel ubiquitination-based mechanism by which CypA regulates the replication of IAV.