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1.
采用扫描电镜技术对腰带长体茧蜂Microcentrus cingulum的触角感器进行了观察.结果表明,腰带长体茧蜂雌蜂触角上存在三种感器,分别为毛形感器、刚毛形感器、板形感器.对触角各种感器的形态和分布特点进行了描述,并就三类触角感器的功能进行了探讨.  相似文献   

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麦蛾茧蜂触角感器的扫描电镜观察   总被引:6,自引:1,他引:5  
应用扫描电镜对麦蛾茧蜂BraconhebetorSay的触角感器进行观察。结果表明:麦蛾茧蜂的触角上存在6种感器,分别为毛形感器,板形感器,刺形感器,鳞状感器,锥形乳头状感器和嗅孔。其中毛形感器和板形感器是主要感器,数量较大,分布较广。雌雄蜂的触角感器差异不明显。  相似文献   

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二化螟盘绒茧蜂触角感器的超微结构   总被引:6,自引:1,他引:5  
周志军  王世贵 《昆虫知识》2005,42(6):676-680
采用扫描电子显微镜对二化螟盘绒茧蜂Cotesia chilonisMunakata触角感器进行了观察和研究。结果表明,二化螟盘绒茧蜂触角上共存在6种感器,分别为板形感器、毛形感器、刚毛型感器、柱形感器、钟形感器、锥形感器。对各种触角感器的形态、分布特点进行了描述,并对两性间的差异及其功能进行了探讨。  相似文献   

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中红侧沟茧蜂触角感受器的扫描电镜观察   总被引:6,自引:0,他引:6  
董文霞  张钟宁 《昆虫学报》2006,49(6):1054-1059
利用扫描电镜对中红侧沟茧蜂Microplitis mediator的触角感受器进行了观察,发现了6个类型的感器,分别为毛形感器、板形感器、刺形感器、钟形感器、锥形感器、腔锥形感器。其中,毛形感器具有2种形态,锥形感器具有4种形态。钟形感器仅分布于雌蜂的触角上,锥形感器Ⅲ和Ⅳ仅分布于雄蜂的触角上。结合感受器的形态、分布和已报道的触角电位反应数据,对各感受器的功能进行了推测。  相似文献   

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虫草蝠蛾触角感觉器的扫描电镜观察   总被引:9,自引:0,他引:9  
本文报道冬虫夏草的三种寄主昆虫白马蝠蛾(Hepialus baimaensis)、 人支蝠蛾(H.Renzhiensis)和中支蚯蛾(H.Zhongzhiensis)触角感觉器种类、形态和分布的扫描电镜观察结果。三种蝠蛾触角表面均缺少网状覆盖物。计有七种感觉器,名称为毛形感器、刺形感器、锥形感器、腔锥感器、Bohm氏鬃毛、鳞形感器和钟形感器。毛形感器分A和B型,数量最多。鞭节上每节具有2-3只刺形感器和l-5只锥形感器。腔锥感器分为长栓和短栓两种形态类型,腔周围都无缘栓。 Bohm氏鬃毛主要分布于基节,数量较多。钟形感器仅在雄蛾触角上见到。各类感觉器在种间无明显差异。  相似文献   

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赵晓英  杨伟  杨桦  杨春平  张犀  黄琼 《昆虫知识》2011,48(6):1792-1797
采用扫描电镜观察了刺粉虱黑蜂Amitus hesperidum Silvestri触角。结果表明,在雌雄蜂的触角上共存在着7种感觉器,分别为Bhm氏鬃毛、毛形感觉器、板形感觉器、腔锥形感器、柱形感觉器、栓锥形感觉器。对触角感觉器的形态、分布进行了描述。雌雄触角有性二型现象,主要表现在毛形感器数量差异明显,板形感器分布不同,栓锥形感器只在雌虫上发现。  相似文献   

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《环境昆虫学报》2013,35(5):635-642
应用扫描电镜(SEM)对桔小实蝇本地寄生蜂长尾全裂茧蜂 Diachasmimorpha longicaudata (Ashmead) 成虫的触角感器进行观察。结果表明:长尾全裂茧蜂成虫触角由柄节、梗节和鞭节组成,鞭节共 49-52小节。在触角上共有 8种感器,分别为 Bhm鬃毛、毛形感器、刺形感器、锥形感器、板形感器、腔锥形感器、钟形感器、嗅孔。毛型感器是主要感器,数量多且分布广,其次为板形感器。除了腔锥形感器 Ⅱ外,雌雄蜂没有明显的二型现象。  相似文献   

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兴安落叶松鞘蛾触角及其感器的扫描电镜观察   总被引:1,自引:0,他引:1  
杨慧  严善春  彭璐 《昆虫知识》2008,45(3):405-417
应用扫描电镜对兴安落叶松鞘蛾Coleophora obducta(Meyrick)触角及其感器进行观察和研究。结果表明,兴安落叶松鞘蛾触角为丝状,其上共有8种感器:板形感器、锥形感器、腔锥形感器、栓锥形感器、毛形感器、鳞形感器、叉形感器和Bhm氏鬃毛,对各种感器的形态、分布特点进行描述,推测其可能具有的功能。雌雄蛾触角有明显的性二型现象,表现为雌雄触角大小不同,触角感器类型、大小、数量、分布不同。  相似文献   

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玉龙蝠蛾触角感觉器的扫描电镜观察   总被引:9,自引:0,他引:9  
本文报道玉龙蝠蛾 Hepialus yulongensis Liang 触角感觉器种类、形态和分布的扫描电镜观察结果。蝠蛾触角呈丝状,由柄节、梗节和21—27个鞭节组成,总长2.3—2.7毫米,柄节比以后各节长,触角表面缺少隆起的网纹。触角感觉器计有七种,其名称为毛形感器、刺形感器、腔锥感器、锥形感器、鳞形感器、Bohm氏鬃毛及仅出现于雄蛾的钟形感器。根据中心栓的长度,腔下陷的深度和直径,腔锥感器基本上可分为长栓和短栓两种形态类型,腔的周围都无向内倾斜的缘栓;毛形感器可进一步分为A型和B型;Bohm氏鬃毛数量多,主要分布于柄节、梗节,但在端节也能见到。  相似文献   

10.
中华蜜蜂工蜂触角感受器的扫描电镜观察   总被引:27,自引:3,他引:24  
杜芝兰 《昆虫学报》1989,32(2):166-169
对中华蜜蜂(Apis cerana)工蜂触角感受器的扫描电镜观察,见到在触角上有九种类型的感受器,它们是板形感器、腔锥感器、坛形感器、钟形感器、锥形感器、毛形感器A、毛形感器B、毛形感器C和D、缘感器以及各种类型的刚毛等.对于这些感受器的外部形态和分布部位进行了详细地观察和描述,发现中华蜜蜂与西方意蜂(Apis mellifera)有差异.  相似文献   

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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.  相似文献   

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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  相似文献   

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