甲维盐·氟铃脲复配剂对甜菜夜蛾的时间-剂量-死亡率模型研究

以甜菜夜蛾 (SpodopteraexiguaH櫣ｂｎｅｒ) 2龄幼虫为试虫 ,测定了 5种配比的甲胺基阿维菌素苯甲酸盐(简称甲维盐 )与氟铃脲混配剂的毒力 ,测定结果建立了“时间 -剂量 -死亡率”模型。根据模型分析结果 ,甲维盐与氟铃脲混配后增效显著 ,5种配比中以甲维盐∶氟铃脲 =1∶10为最佳配比。其 2 4～ 6 0h 4个时段的共毒系数在 4 0 0～ 6 0 0之间 ,用 2 0、 1 0 μg·mL- 1浓度处理后的LT50 分别为 18 4 6和 30 5 8h     

甲维盐·毒死蜱及其复配对小菜蛾的毒力分析

以小菜蛾（Plutella xylostellar） 3龄幼虫为试虫测定了甲胺基阿维菌素苯甲酸盐、毒死蜱及两者5种不同配比的复配剂的毒力,测定结果建立了“时间-剂量-死亡率”模型.根据模型分析结果,甲胺基阿维菌素苯甲酸盐与毒死蜱混配后增效显著.在5种配比中以甲氨基阿维菌素苯甲酸盐∶毒死蜱 =1∶ 74为最佳配比,其24-60 h 4个时段的共毒系数在334到550之间;与单剂相比,该配比明显提高了24 h时段内和48-60 h时段的杀虫率.     

几类杀虫剂对灰飞虱的相对毒力及田间种群的抗药性现状

采用浸苗法测定了6类11种杀虫剂对灰飞虱Laodelphax striatellus (Fallén)3龄若虫的毒力,并分析比较了江苏句容、通州、楚州、大丰、南京和苏州以及安徽庐江等7地灰飞虱种群对10种杀虫剂的抗药性水平。对云南种群而言,在所测杀虫剂中,以乙酰甲胺磷为标准药剂,氟虫腈的相对毒力最高;噻嗪酮、阿维菌素和噻虫嗪次之;高效氯氰菊酯、IPP（硝基亚甲基类化合物）、毒死蜱、敌敌畏和三唑磷间毒力处于同一数量级,低于阿维菌素等杀虫剂;吡虫啉的相对毒力最低。与云南种群相比,2007年采自苏、皖7个不同地区的灰飞虱种群对噻嗪酮产生了极高水平的抗性,其抗性倍数均超过200倍;对高效氯氰菊酯产生了中高水平的抗性,其抗性倍数为7.8～108.8;安徽庐江灰飞虱种群对三唑磷产生了7.7倍的抗性,对毒死蜱产生了12.0倍的抗性,江苏楚州、南京、大丰和句容灰飞虱种群对毒死蜱产生了5.7～12.6倍的抗性; 所有灰飞虱种群对敌敌畏仍然敏感,对氟虫腈、阿维菌素和新烟碱类杀虫剂吡虫啉、噻虫嗪和IPP等也比较敏感。     

nC22矿物油及其与吡虫啉混用对柑橘木虱的室内毒力评价

【目的】室内评价nC22矿物油单独使用,以及与吡虫啉混用对柑橘木虱Diaphorina citri的毒力,并筛选nC22矿物油对吡虫啉防治柑橘木虱具有增效作用的混配比例,为矿物油防治柑橘木虱的应用提供科学依据。【方法】使用nC22矿物油以及阳性对照nC23和nC28矿物油,采用浸渍法和喷雾法分别检测矿物油对柑橘木虱卵和低龄若虫、高龄若虫、成虫的致死作用,以处理后第7天(卵)和第1天(若虫和成虫)的LC₅₀值评估毒力。将nC22矿物油与吡虫啉以不同配比混配,测定混配液对低龄若虫的毒力,使用交互测定法、共毒因子(co-toxicity factor, CTF)法和共毒系数(co-toxicity coefficient, CTC)法评价矿物油对吡虫啉的增效作用。【结果】单独使用时,nC22矿物油对卵的LC₅₀值低于nC23和nC28矿物油;对低龄若虫和高龄若虫的LC₅₀值与nC23矿物油相当,都低于nC28矿物油;对成虫的LC₅₀值与nC28矿物油相当,都低于nC23矿物油。与吡虫啉混用时,nC22矿物...     

三种药剂及其复配剂对松突圆蚧的毒力测定

本以机油乳油、毒死蜱及喹硫磷对松突圆蚧1龄若虫进行室内毒力测定,结果表明各药剂对松突圆蚧均有一定的毒力,其中喹硫磷的毒力明显大于其它两种药剂的毒力,但喹硫磷与毒死蜱及机油复配没有增效作用,而机油乳油与毒死蜱以13：10混配,增效作用明显,共毒系数达到405．41．     

叶蝉散与杀虫双混剂的药效测定

室内毒力测定结果表明,叶蝉散与杀虫双混配剂对稻褐飞虱表现有增效作用。其中以1:1混配剂增效作用较为明显,共毒系数为175.6,增效倍数约为1.8倍;1:2和1:3混配剂的共毒系数分别为150.7和137.3,增效倍数约为1.5倍和1.4倍。从而为叶蝉散与杀虫双混剂的开发提供了科学依据。     

混配杀虫剂对烟蚜的毒力测定

选用氰戊菊酯乳油为底药,与其它3种药剂分别按有效成份进行不同比例的混配,测定其对烟蚜的毒力差异.实验结果表明:氰戊菊酯乳油与辛硫磷乳油按3:2进行混配时,其共毒系数最大,为825.96;其次是按1:1进行混配时,其共毒系数为462.45;最小的为2:3进行混配时,其共毒系数为244.62.氰戊菊酯乳油与灭多威乳油按1:1进行混配时,其共毒系数最大,为367.09;其次是按3:2进行混配时,其共毒系数为297.08;最小的为2:3进行混配时,其共毒系数为157.32.氰戊菊酯乳油与吡虫啉按2:3进行混配时,其共毒系数最大,为1558.28;其次是3:2进行混配时,其共毒系数为603.01;最小的为1:1进行混配时,其共毒系数为326.13.各个配比的共毒系数均大于100,均表现出增效作用.     

吡虫啉和杀虫单混配对稻纵卷叶螟的毒力测定

室内进行吡虫啉和杀虫单混配对稻纵叶螟的毒力测定,测定结果表明:吡虫啉和杀虫单不同配比的混合物对稻纵叶螟均有一定的增效作用,其中吡虫啉∶杀虫单(1∶29)混配物增效作用最为显著。     

不同农药对木瓜秀粉蚧的毒力及复配增效作用

为筛选对入侵害虫木瓜秀粉蚧毒力较好的农药及复配增效配比,为该虫的化学药剂防治提供理论依据,本文采用叶面喷雾法测定了11种农药对木瓜秀粉蚧2龄若虫的室内毒力,挑选毒力较好的两种药剂进行复配,筛选增效配比,并进行田间药效试验。结果表明,11种农药对木瓜秀粉蚧的毒力大小依次为:螺螨酯>哒螨灵>噻虫胺>联苯菊酯>矿物油>高效氯氰菊酯>炔螨特>啶虫脒>吡虫啉>噻螨酮>四螨嗪。哒螨灵与螺螨酯(60∶40)复配共毒系数最大,为182.47。田间药效试验发现,混配药剂防效均高于单剂且达到差异显著。     

5种杀虫剂对入侵害虫椰子织蛾的室内毒力测定

椰子织蛾是一种外来新入侵害虫,对棕榈科植物造成了严重危害。采用叶片浸渍法测定了甲维盐等5种杀虫剂对入侵害虫椰子织蛾5～6龄幼虫的室内毒力。5种药剂处理72 h后的室内毒力大小顺序为甲维盐＞氯虫苯甲酰胺＞毒死蜱＞高效氯氟氰菊酯水乳剂＞烟碱;72 h 致死中浓度（ LC50）为5．2604、9．7126、24．8202、104．0584、643．1496 mg· L-1。选取同样毒力效果所需成本依次为毒死蜱＜甲维盐＜高效氯氟氰菊酯＜氯虫苯甲酰胺＜烟碱。本研究可用于指导椰子织蛾的应急化学防控。综合毒力和成本,建议在生产上采用毒死蜱和甲维盐等相关药剂防治椰子织蛾。     

Investigation of the mechanism of temperature sensitivity of the electroreceptors of ampullae of lorenzini

In experiments on Black Sea skates (Raja clavata), the potential of the receptor epithelium of the ampullae of Lorenzini and spike activity of single nerve fibers connected to them were investigated during electrical and temperature stimulation. Usually the potential within the canal was between 0 and –2 mV, and the input resistance of the ampulla 250–400 k. Heating of the region of the receptor epithelium was accompanied by a negative wave of potential, an increase in input resistance, and inhibition of spike activity. With worsening of the animal's condition the transepithelial potential became positive (up to +10 mV) but the input resistance of the ampulla during stimulation with a positive current was nonlinear in some cases: a regenerative spike of positive polarity appeared in the channel. During heating, the spike response was sometimes reversed in sign. It is suggested that fluctuations of the transepithelial potential and spike responses to temperature stimulation reflect changes in the potential difference on the basal membrane of the receptor cells, which is described by a relationship of the Nernst's or Goldman's equation type.I. P. Pavlov Institute of Physiology, Academy of Sciences of the USSR, Leningrad. I. M. Sechenov, Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Pacific Institute of Oceanology, Far Eastern Scientific Center, Academy of Sciences of the USSR, Vladivostok. Translated from Neirofiziologiya, Vol. 12, No. 1, pp. 67–74, January–February, 1980.     

Principles of organization and evolution of systems of regulation of functions

Evolution of living organisms is closely connected with evolution of structure of the system of regulations and its mechanisms. The functional ground of regulations is chemical signalization. As early as in unicellular organisms there is a set of signal mechanisms providing their life activity and orientation in space and time. Subsequent evolution of ways of chemical signalization followed the way of development of delivery pathways of chemical signal and development of mechanisms of its regulation. The mechanism of chemical regulation of the signal interaction is discussed by the example of the specialized system of transduction of signal from neuron to neuron, of effect of hormone on the epithelial cell and modulation of this effect. These mechanisms are considered as the most important ways of the fine and precise adaptation of chemical signalization underlying functioning of physiological systems and organs of the living organism