革螨跗感器的结构和功能

本文进一步研究了:④厩真厉螨截肢前后的爬行行为,表明第1对足其感觉功能;②用古拉广厉螨分别截各对足驱避反应的对比试验,见到只有当截去第1对足跗节时失去嗅觉功能,而截去第Ⅱ、Ⅲ、Ⅳ对足时,各组都仍有嗅觉功能;⑤对格氏血厉螨、厩真厉螨、毒厉螨和鼠颚毛厉螨进行涂漆前后的驱避试验,显示当跗感器被涂满封闭,则嗅觉功能消失;④以0.5%结晶紫或龙胆紫液染色的截肢标本,观察了厩真厉螨、毒厉螨、格氏血厉螨、古拉广厉螨及尾足螨股一种螨,足Ⅰ跗节末端凹窝中,至少都存在两类感毛,钝钉型感毛和长而尖的刚毛型感毛;⑤厩真厉螨雌螨和幼螨跗感器的钝钉毛分别为8根和5根,另外各有2根短而尖的毛,分别测定了长度,描述了形态特点;⑥透射电镜观察厩真厉螨、毒厉螨等的跗感器钝钉毛,毛外围有表皮壁,壁上有很多微孔,内有中心腔,腔内有树突。属化感器——嗅觉器;⑦电生理技术研究,当用氨和醋酸的气体刺激厩真厉螨、毒厉螨的离体足Ⅰ时,均产生明显的应激电位差,充分证明足Ⅰ辩节有嗅觉功能。     

新蚤属斯氏组一新种记述(蚤目:猬形蚤科)

在1960年我们从四川省阿坝地区的几种啮齿动物体上,采到一些跳蚤标本,经鉴定后,其中发现新蚤属(Neopsylla Wagner,1903)一新种,该新种属于斯氏组(Stevensi group),订名为鞍新蚤新种N.sellaris sp.nov.。 鉴别特征 鞍新蚤新种以其雄性阳茎内突端附器为杆形,抱器突起的形状,第Ⅸ腹板后臂的形状和雌性第Ⅶ腹板后缘的凹陷很浅,与N.anoma Rothschild,1912相近似;又以其前、中足第Ⅴ跗节具4对侧蹠鬃,后足第Ⅴ跗节仅具3对侧蹠鬃而与N.luma Traub,     

中国岩螨属一新种记述(蜱螨目:叶螨科)

岩螨属(Petrobia Murray,1877)雌螨背面观椭圆形,具3对前足体背毛,9对后半体背毛和1对肩毛。背毛均不着生在结节上。足Ⅰ跗节具2对双毛。跗节爪垫状,具粘毛。爪间突钩状,具2列指向腹侧的粘毛。     

齿缘刺猎蝽成虫触角和跗节感器的扫描电镜观察

利用扫描电镜观察了齿缘刺猎蝽(Sclomina erinacea Stal)成虫触角及前足跗节上的感受器,结果表明:齿缘刺猎蝽触角5节,由柄节、梗节和3个鞭节构成,梗节最短;雌、雄虫前足跗节均为3节。触角上共有3种感器,分别为毛形感器、刺形感器和锥形感器,其中,毛形感器、锥形感器各有两种类型,刺形感器有3种类型。雌、雄个体间触角感器类型及分布未见明显差异。前足跗节上仅存在刺形感器,该感器在雄虫前足跗节上的分布较雌虫密集。     

叶螨科一新属新种(蜱螨目)

1974年在广东省海南岛地区,采到一种为害新会橙的叶螨,确定为一个新属新种。描述如下: 刺爪螨属 Acanthonychus,新属 前足体背毛3对,后半体背毛10对;背毛粗壮,具锯齿,着生于明显的突起上。足Ⅰ跗节具2对双毛,足Ⅱ跗节具1对双毛。跗节爪退化,各具1对粘毛;爪间突呈直角弯曲,     

蚌螨腺毛和足爪的亚显微结构观察

利用扫描电镜分别对6种蚌螨的腺毛和足爪结构进行了观察,结果表明蚌螨的腺毛是由腺体、围腺片、刚毛和腺毛板共同构成的复合结构;对弯弓蚌螨的连续切片的观察表明,腺体是从体表延伸至体腔的消化道附近,由此认为蚌螨的腺体是由体壁皮层细胞演化而来。蚌螨足末除了爪外,还观察到跗节端部背面或腹面有体壁突及刚毛,因此,蚌螨足的步行结构不是仅由爪形成的简单结构,而是由爪、跗节末端背突或腹垫和刚毛组成的复合体。     

雄蚤生殖节的扫描电镜观察

本文利用扫描电镜对雄蚤生殖节表面细微结构进行了观察,发现了一些光镜下不易看到的纹理状结构和小棘及一些感器.这些微小的纹理状结构和小棘在不同蚤种之间有差异,这种差异具有相对的稳定性,可望用于蚤的亚显微水平的分类.通过对感器的观察,发现生殖节上具有大量的毛形感器,另外还观察到有锥形感器、短锥形感器、钟形感器、栓锥感器、腔锥感器及刺形感器等.这些感器的数量分布及有无因种而异.这些感器的存在与交配行为密切相关,作者对此也进行了讨论.     

中国叶螨科一新属新种(蜱螨目)

在云南大理的竹子上采到一种叶螨,经鉴定是叶螨族Tetranychini Reck,1950的一新属新种。描述如下(文内量度单位为微米)。 云爪螨属Yunonychus新属 前足体背毛3对,后半体有肩毛1对,背中毛3对,背侧毛2对,骶毛2对,臀毛1对;第一对背侧毛缺如。腹面有肛毛和肛侧毛各2对,爪间突粗壮,开裂为二,爪状。足Ⅰ跗节有双毛2对,足Ⅱ跗节有双毛1对。     

大豆蚜触角嗅觉感器结构及其功能

采用扫描电镜观察大豆蚜Aphis giycines各型触角上嗅觉感器的细微结构,结合触角电位记录,发现大豆蚜有翅孤雌生殖蚜对萜烯衍生物的感受部位在第6节原生感器上,而萜烯烃类则在第5节原生感器上,两原生感器都对绿叶气味和芳香类起嗅觉反应。末端2节上还有其它化学感器对植物气味起反应。因此,各型对植物气味的感觉部位在末端2节上。各型对报警信息素的作用部位主要在第6节原生感器上,无翅型第5节原生感器和有翅型第3节次生感器也有一定的感觉能力。     

三种蝇类昆虫(双翅目)足爪垫结构的超微形态研究

利用扫描电子显微镜对双翅目3种蝇类昆虫即家蝇Musca domestica L.(蝇科)、红尾粪麻蝇Bercaea cruentata(Meigen)(麻蝇科)和肥躯金蝇Chrysomya pinguis (Walker)(丽蝇科)足的爪垫超微形态结构进行了研究,研究发现每种蝇类的前、中、后足爪垫的面积存在一定的差别,中足和后足爪垫面积较前足大;爪垫腹面均密被刚毛,每根刚毛由刚毛杆(setal shaft)和末端平板(terminal plate)组成,刚毛主要有铲状、勺状和柳叶状3种类型;后足爪垫上刚毛的密度和刚毛末端面积一般小于前、中足;位于爪垫边缘处的刚毛较长.研究还发现爪垫上的刚毛均为中空结构,且丽蝇科昆虫的刚毛末端具开口.     

Central projections of sensory cells of the midleg of the locust,Schistocerca gregaria

The central projections of trichoid hairs and of some scolopidial organs of the mesothoracic leg of the locust Schistocerca gregaria were studied by using nickel chloride backfilling and single cell recording. Trichoid hair sensilla on different parts of the legs project somatotopically in the ventral part of the ipsilateral neuropile of the mesothoracic ganglion. Generally, distally located receptors have their terminal arborizations in ventro-lateral areas of the neuropile, and proximally located receptors in ventro-medial areas. The axons of the subgenual organ and tarsal chordotonal organs project into the intermediate neuropile.     

Sex-specific non-pheromonal taste receptors in Drosophila

Taste receptors have recently been reported in Drosophila [1,2], but little is known of the relation between receptor and response. Morphological studies of the distribution of chemosensory sensilla indicate that the fruit fly has two major sites of gustation: the proboscis and the legs [3]. The taste sensilla on both these sites are similar in structure and each sensillum generally houses four gustatory neurons [4]. Early anatomical observations have demonstrated a sexual dimorphism in the number of tarsal sensilla [5] and in their central projections [6]. We measured the electrophysiological responses of the prothoracic taste sensilla to non-pheromonal substances--salts, sugars and water--and found a clear sexual dimorphism. From the response profile of individual sensilla, we were able to distinguish three types of tarsal sensilla in females as against only two types in males. The female-specific type, which responded specifically to sugar, was absent in males except when male gustatory neurons were genetically feminised. The fact that tarsal gustatory hairs exhibit a sexual dimorphism that affects the perception of non-pheromonal compounds suggests that sexual identity is more complex than has previously been thought [7,8].     

Sex-specific non-pheromonal taste receptors in Drosophila

Taste receptorshave recently been reported in Drosophila [1] and [2], but little is known of the relation between receptor and response. Morphological studies of the distribution of chemosensory sensilla indicate that the fruit fly has two major sites of gustation: the proboscis and the legs [3]. The taste sensilla on both these sites are similar in structure and each sensillum generally houses four gustatory neurons [4]. Early anatomical observations have demonstrated a sexual dimorphism in the number of tarsal sensilla [5] and in their central projections [6]. We measured the electrophysiological responses of the prothoracic taste sensilla to non-pheromonal substances—salts, sugars and water—and found a clear sexual dimorphism. From the response profile of individual sensilla, we were able to distinguish three types of tarsal sensilla in females as against only two types in males. The female-specific type, which responded specifically to sugar, was absent in males except when male gustatory neurons were genetically feminised. The fact that tarsal gustatory hairs exhibit a sexual dimorphism that affects the perception of non-pheromonal compounds suggests that sexual identity is more complex than has previously been thought [7] and [8].     

Adaptation of sensory systems of gamasid mites (Parasitiformes, Gamasina) to dwelling in different environment

The main complication sensory organs (the palpal organ and the tarsal sensory complex) of several species of gamasid mites were studied in scanning electron microscope. The species examined included permanent ectoparasites (Laelaps agilis, Laelaptidae), parasites of the nasal cavity and respiratory tract of birds (Sternostoma tracheocolum and Ptilonyssus reguli, Rhinonyssidae), dwellers of the sea littoral zone (Parasitus kempersi, Parasitus immanis, Parasitidae), and mites found on soil and on plants (Amblyseius barkeri, Parasitidae). Similar sensillar types, including olfactory SW-WP sensilla, contact chemo-mechanosensory (SW-UP and DW-UP) sensilla, termo-chemo-mechanosensitive (DW-WP) sensilla of two types, and tactile (NP) sensilla were found in all these species, excluding endoparasites, where some sensillar types (in particular, DW-WP sensilla with slit-like pores) are absent. It was shown that the topography of olfactory SW-WP sensilla of the tarsal complex reflects taxonomic position and phylogenetic history of mite genera, whereas the number of certain sensillar types and the degree of their development reflect ecological specialization of species. The palpal organ is characterized by rather uniform structure in mites of different families, dwellers of different environments, except for the endoparasites of the family Rhinonyssidae, where this organ is strongly reduced.     

Ultrastructure of the antennal sensilla of the cockroach-egg parasitoid,Tetrastichus hagenowii (Hymenoptera: Eulophidae)

Eggs of a number of cockroach species are parasitized by Tetrastichus hagenowii. The ultrastructure of the sensilla on the antennae of females and males was examined by scanning and transmission electron microscopy. The females have two types of multiporous plate sensilla while the males have only one. Type 1 is found in females and males and has a relatively thin cuticular wall and many pores, while type 2 is found only in females and has a relatively thick cuticular wall and few pores. Both sexes have nonporous, thick-walled, socketed hairs; multiporous, nonsocketed hairs; multiporous, thick-walled pegs; and terminal hairs. In addition, males have multiporous, nonsocketed, long hairs. The sensilla are similar, in many respects, to the sensilla of other chalcid parasitoids. The antennal sensilla of female T. hagenowii are probably involved in ovipositional behavior. The multiporous, long hairs of the male possibly receive stimuli during mating behavior A chemoreceptive function is proposed for the multiporous plate sensilla.     

Detection of vibrations in sand by tarsal sense organs of the nocturnal scorpion,Paruroctonus mesaensis

Summary The scorpionParuroctonus mesaensis locates prey by orienting to substrate vibrations produced by movements of the prey in sand. At the end of each walking leg of this scorpion there are two sense organs, the basitarsal compound slit sensillum and tarsal sensory hairs (Figs. 1, 3) that are excited by substrate vibrations conducted through sand. The slit sensilla appear to be most sensitive to surface (Rayleigh) waves while the tarsal sensory hairs respond best to compressional waves (Fig. 7). Both mechanoreceptors were activated by nearby disturbances of the substrate (Fig. 6) but only the slit sensilla responded to insects moving more than 15 cm away. Both receptors are highly sensitive to small amplitude (less than 10 Å) mechanical stimuli applied to the tarsus (Fig. 5).Behavioral studies of scorpions with ablated sense organs (Fig. 2) indicate that the basitarsal compound slit sensilla are necessary for determining vibration source direction.Abbreviation BCSS basitarsal compound slit sensillum (a) Supported by PHS Environmental Science and Regents Intern Fellowships (PB), and by intramural research funds from the University of California (RDF)     

External morphology of antennae and their sense organs in the roach Gromphadorhina brunneri (Blattoidea: Dictyoptera)

The antennae and their sense organs in nymphs and adult roaches of Gromphadorhina brunneri, were investigated and described. The number of segments and sensillae of the nymphal antennae depend on the developmental stage. Sexual dimorphism is pronounced. Males have longer antennae than females as well as an abundance of especially long sensory hairs (long wavy hairs), which are probably responsible for the perception of female sex pheromones. They also have more thin-walled sensory hairs, for instance, sensilla trichodea. On a morphological basis the sensillae of Gromphadorhina brunneri, were named and classified. Long wavy hairs and large sensory hairs appear to be present also in a related species, G. portentosa, but are lacking in others. Their distribution on the antennae varies greatly from that in G. portentosa but their structure varies only slightly. These two types of sense organs are considered to be specialized forms of sensilla chaetica. They are contact chemoreceptors, as are two other types of sensilla chaetica. Furthermore, thin-walled chemoreceptors are present, such as sensilla trichodea, sensilla basiconica, sensilla coeloconica and a typical mechanoreceptor, the sensillum campaniformium.     

Functional anatomy of sensory structures on the antennae of Psylliodes chrysocephala L. (Coleoptera: Chrysomelidae)

The ultrastructure and distribution of sensilla on the antennae of the cabbage stem flea beetle, Psylliodes chrysocephala, were investigated using scanning and transmission electron microscopy techniques. Eight different sensillar types were distinguished. These were; hair plate sensilla, sensilla chaetica, three types of sensilla trichodea, sensilla basiconica, grooved peg sensilla and styloconic sensilla. The sensilla chaetica are known to be gustatory receptors. Ultrastructure indicates that the hair plate sensilla and sensilla trichodea type one are probably mechanoreceptors, whilst the sensilla styloconica are probably thermo-hygro receptors. These thermo-hygroreceptors are unusual in that they are innervated by two sensory cells (one hygroreceptor and one thermoreceptor) rather than the more usual triad. The remaining four sensillar types all have a porous hair shaft, indicating an olfactory role. One of these (the grooved peg sensillum) may also have a thermoreceptive function. No sexual dimorphism was found in the structure, number or distribution of the antennal sensilla.     

Fine structure of tarsal sensory organs in the whip spider Admetus pumilio (Amblypygi, Arachnida).

The sensory organs on the tarsi of the antenniform first legs of the whip spider Admetus pumilio C. L. Koch (Amblypygi, Arachnida) were examined with the scanning and transmission electron microscope. At least four different types of hair sensilla were found: (1) thick-walled bristles, which have the characteristics of contact chemoreceptors (several chemoreceptive dendrites in the lumen plus two mechanoreceptors at the base); (2) short club sensilla, innervated by 4-6 neurons which terminate in a pore on the tip; they are possibly humidity receptors; (3) porous sensilla, which are either innervated by 20-25 neurons and have typical pore tubules, or they have 40-45 neurons but no pore tubules; both types are considered to be olfactory; (4) rod sensilla occur in clusters near segmental borders; they are innervated by only one large dendrite which branches inside the lumen. Other tarsal receptors are the claws, which correspond to contact chemoreceptors, and the pit organ which resembles the tarsal organ of spiders. Compared to other arthropod sensilla, the contact chemoreceptors are very similar to those of spiders, while the porous sensilla correspond structurally to olfactory receptors in insects; the club and rod sensilla seem to be typical for amblypygids.     

The cercal receptor system of the praying mantid,Archimantis brunneriana Sauss.

Summary The cerci of the praying mantid, Archimantis brunneriana Sauss., are paired segmented sensory organs located at the tip of the abdomen. Basally the cercal segments are slightly flattened dorso-ventrally and are fused to such a degree that it is difficult to distinguish them. Distally the segments become progressively more flattened laterally and their boundaries become more obvious.Two types of sensilla are present on the cerci, trichoid sensilla and filiform sensilla. Trichoid hairs are longest on the medial side of the cerci and toward the cercal base. On the proximal cercal segments they are grouped toward the middle of each segment while they are more uniformly distributed on the distal segments. Filiform sensilla are found at the distal end of each segment except the last and are most abundant on the middle segments of the cercus. Both the number of cercal segments and the number of sensilla are variable. Trichoid hairs are highly variable in appearance from short and stout to long and thin. They arise from a raised base, have a fluted shaft, and some have a pore at the tip. They are innervated by from one to five dendrites, one of which is always considerably larger than the others. Some of the dendrites continue out into the shaft of the hair.Filiform hairs have fluted shafts and are mounted in a flexible membrane within a cuticular ring in a depression. They are innervated by a single large sensory neuron, the dendrite of which passes across a flattened area on the inner wall of the lumen of the hair. The dendritic sheath forms the lining of the ecdysial canal and is therefore firmly attached to the hair. The dendrite is attached to the sheath by desmosomes distally and is penetrated by projections of the sheath more proximally. A fibrous cap surrounds the dendrite and may hold it in place relative to the hair.The cercal receptor system of Archimantis is compared to those of cockroaches and crickets.