Sensilla on the third antennal segment of Drosophila melanogaster meigen (Diptera : Drosophilidae)

The distribution and morphology of the sensilla on the 3rd antennal segment of Drosophila melanogaster Meigen (Diptera : Drosophilidae) were studied with light and electron microscopy. Four types of hairs were identified. Three types of hairs innervated by dendrites are sensilla basiconica, sensilla coeloconica and sensilla trichodea. They occur amongst a large number of the 4th type of uninnervated hairs or spinules.Sensilla basiconica and coeloconica can be easily identified by light microscopy on staining with 0.1016 silver nitrate in 70% ethanol. The tips of sensilla basiconica and coeloconica appear dark brown. Most of the sensilla trichodea and spinules remain unstained.Sensilla basiconica conform to the single-walled, multiporous sensilla, having poretubules and branched dendrites. Sensilla coeloconica are double-walled and have longitudinal channels near the tip. No wall pores are found on sensilla trichodea. Dendrites do not branch in sensilla coelonica and trichodea. A mechanosensory dendrite with characteristic tubular body is absent in these sensilla.Populations of sensilla basiconica and sensilla trichodea occur in diametrically opposite, distinct regions on the 3rd antennal segment-the former in the dorsomedial and the latter in the ventrolateral regions, whereas sensilla coeloconica are distributed on most of the anterior and posterior surfaces, including the cavity walls of the sacculus.The axons are arranged in distinct groups in the antennal nerves at the stalk of the 3rd segment. This grouping becomes more pronounced in the nerve prior to its entry into the brain.     

Ultrastructure of the antennal sensilla of the mayfly Baetis rhodani (Pictet) (Ephemeroptera : Baetidae)

The distribution and fine morphology of antennal sensilla of nymphal and adult mayfly, Baetis rhodani (Ephemeroptera : Baetidae), were examined. In the nymph, various kinds of sensilla (chaetica, basiconica, coeloconica and cuticular pits) are differently arranged on the antennal segments, whereas sensilla campaniformia delimit the distal border of the pedicel. A peculiar kind of sensillum basiconicum, named flat-tipped sensillum, is present along the entire antenna, even though in the flagellum it has a regular arrangement between the cuticular lobes that delimit the distal border of each article. In the subimago the scape and pedicel are profusely covered with microtrichia and scattered sensilla trichodea, whereas the flagellum shows cuticular ribs. Sensilla coeloconica are present along the ventral side of the flagellum. In the imago, the antenna is completely decorated with scales among which sensilla trichodea and sensilla coeloconica occasionally occur. As in the nymph, adult mayflies have a ring of sensilla campaniformia along the distal border of the pedicel. When compared with nymphal antennae, those of adults have fewer types of sensilla, presumably in relation to the short, non-feeding terrestrial life.     

Sensilla on maxillary and labial palps in a helicophagous ground beetle larva (Coleoptera,Carabidae)

Sensilla on the labial and maxillary palp of Carabus lefebvrei Dejean, 1826 larvae were investigated using scanning and transmission electron microscopy. Two identical sets of sensilla were present on the tips of both palp pairs, and four morphological types of sensilla were identified: sensilla basiconica types 1 and 2, sensilla coeloconica and sensilla digitiformia. Ultrastructure indicates that the sensilla basiconica type 1 and coeloconica have a chemical role as gustatory and olfactory receptors, respectively, while sensilla basiconica type 2 are mechanoreceptors and the sensilla digitiformia are probably thermo‐ and hygroreceptors. Their function is discussed in relation to specialized prey detection and habitat adaptations.     

Description of the antennal sensilla of <Emphasis Type="Italic">Habrobracon Hebetor</Emphasis>

The morphology of the antennal sensilla of both male and female Habrobracon hebetor (Say) (Hymenoptera: Braconidae) is described using Scanning Electron Microscopy complemented with Transmission Electron Microscopy. Five types of innervated sensilla as well as uninnervated microtrichia were found. These types are: sensilla trichodea; s. chaetica; s. basiconica; s. coeloconica; and s. placodea. No differences in shape, basic structure, and types of antennal sensilla were found between males and females. The types of sensilla of both sexes of H. hebetor were compared with what has been described in other parasitic Hymenoptera, and their putative functions are discussed with reference to their morphology, distribution and ultrastructure.     

Cuticular structures on the antennae of Hypoderma bovis De Geer (Diptera : Oestridae) females

The antennae of Hypoderma bovis (Diptera: Oestridae) females were examined using scanning electron microscopy. Each antenna is composed of 3 parts: the scape, the pedicel, and the funiculus, with a large, protruding arista. Mechanoreceptors are found on the proximal and lateral margins of the scape and pedicel, respectively. Microtrichia, which are presumably non-innervated, are located evenly over both the outer surface of the scape and the inner surface of the pedicel. A narrow band of microtrichia is present proximally on the outer surface of the pedicel. The entire funicular surface is densely covered with microtrichia. Small patches lacking these microtrichia appear as depressions or “pits” (8–20 μm in diameter) on the surface of the funiculus. Olfactory sensilla found on the funicular surface include basiconica type 1, basiconica type 2, and trichoid sensilla. The sensilla basiconica commonly occur in pits on the anterodorsal surface of the funiculus. Trichoid sensilla are abundant on the posteroventral surface of the funiculus and do not appear to occur in pits. In addition, clavate and peg sensilla, whose functions are unknown, are found in low numbers on the funicular surface. There may be as many as 300 olfactory pits on the anterodorsal surface of each funiculus. These are single-chambered and contain 6 or fewer sensilla basiconica. We propose that a relatively high number of pits may be characteristic of flies in Superfamily Oestroidea (as compared with those of Superfamily Muscoidea), but that pit morphology within the Calyptratae is not Superfamily-specific.     

Sense organs on the ovipositor of Macrocentrus cingulum Brischke (Hymenoptera: Braconidae): their probable role in stinging,oviposition and host selection process

Parasitoid wasps from the insect order Hymenoptera can be deployed successfully as biological control agents for a number of pests, and have previously been introduced for the control of corn pest insect species from the Lepidopteran genus Ostrinia. Organs on the ovipositor of parasitoid wasps have mechanical and tactile senses that coordinate the complex movements of egg laying, and the ovipositor of Hymenopteran insects have evolved associated venom glands as part of their stinging defense. The ovipositor of parasitic wasps has evolved an additional function as a piercing organ that is required for the deposition of eggs within suitable host larvae. The morphology and ultrastructure of sense organs on the ovipositor and sheath of Macrocentrus cingulum Brischke (Hymenoptera: Braconidae) are described using scanning and transmission electron microscopy. Three types of sensilla trichodea were shown to be abundant on the outer sheath of the ovipositor, with types II and III being most distal, and the inner surface of the ovipositor covered with microtrichia, more densely near the apex. Sensilla coeloconica are distributed on both ventral and dorsal valves, while campaniform sensilla and secretory pores are only located on the dorsal valve. The olistheter-like interlocking mechanism, as well as the morphology of the ventral and dorsal valve tips and the ventral valve seal may be important in stinging, oviposition and in the host selection process.     

The antennal sensilla of the adult of Libellula depressa (Odonata: Libellulidae)

An ultrastructural investigation (SEM, TEM) on the antennal flagellum of the adult of the dragonfly Libellula depressa (Odonata:Libellulidae) revealed sensilla located in pits on the lateral-ventral side of the antenna. These sensilla are represented by sensilla coeloconica and by deeply sunken sensilla. The sensilla coeloconica are innervated by three unbranched dendrites, which enter the peg and show a dendrite sheath ending at the base of the peg. The peg has no socket and its cuticle is irregular with wide pore-like structures at the base of which actual pores are visible. The structure of these coeloconic sensilla is in agreement with that reported for single-walled insect chemoreceptors. The deeply sunken sensilla are represented by two kinds of sensilla styloconica, named type-1 and type-2, located at the bottom of deep cavities appearing as simple openings on the antennal surface. These sensilla are no-pore sensilla with inflexible socket and unbranched dendrites and, notwithstanding their structural differences, share common features typical of thermo/hygroreceptors. The presence of chemoreceptors in adult dragonflies sheds light on evolutionary trends in insect perception; the previously unknown occurrence of thermo/hygroreceptors in dragonflies is very important in view of the reported ability of Odonata to thermoregulate heliothermically.     

Consistent pattern in the placement of taste sensilla on the labellar lobes of Aedes aegypti

The long sensilla on the labellar lobes of Aedes aegypti were studied using scanning electron microscopy. The surface of the labella is populated by 3 hair-like structures: long sensilla (female 33.5 μm, SD 3.81 n=114; male 32.0 μm, SD 2.69 n=20), short sensilla (female 4.27 μm, SD 0.550 n=15; male 4.52 μm, SD 0.609 n=15), and microtrichia (female 5.00 μm, SD 0.656 n=55; male 5.27 μm, SD 0.376 n=53). This current study is concerned with the long sensilla. The ventral surface of the labella is consistently populated with 10 long sensilla. The dorsal surface is populated by 5 long sensilla. We assigned the base of each sensillum Cartesian co-ordinates describing its relationship to the other sensilla on the ventral and dorsal surfaces of each individual. These Cartesian co-ordinates were pooled and a stringent form of cluster analysis was used to determine if these sensilla could be identified by location on the labella. Sensilla from different individuals are more closely related by position than sensilla on the same individual, suggesting that these sensilla are located in a consistent pattern over the labellar surface. Sensilla were labeled V1–V10 and D1–D5 on the ventral and dorsal surfaces respectively.     

小菜蛾成虫喙管感器的超微结构及其神经元中枢投射

【目的】明确小菜蛾Plutella xylostella成虫喙管感器的形态结构及感器神经元的投射。【方法】利用扫描电子显微镜观察小菜蛾成虫喙管结构和感器,利用神经回填技术和激光共聚焦显微镜观察喙管感器神经元在脑部的投射。【结果】小菜蛾成虫喙管上存在毛形感器(两种亚型)、腔锥形感器、锥形感器、刺形感器和栓锥形感器5种不同类型的感器。毛形感器表面光滑,分布于外颚叶外侧,可分为毛形感器Ⅰ型和Ⅱ型两种亚型,其中Ⅰ型比Ⅱ型长;锥形感器分布于喙管外表面,由一个感觉锥和一个短的圆形基座组成;腔锥形感器仅分布于食管内侧,只有一个粗短感觉锥而无基座;刺形感器由一个细长的感觉毛和一个圆形基座组成,表面无孔,分布于喙管的外表面;栓锥形感器是昆虫喙管上最典型的感受器,集中分布于喙管顶端区域,感器顶部凹腔伸出一个单感觉锥。此外,喙管上的感觉和运动神经元投射到初级味觉中枢咽下神经节。【结论】本研究阐明了小菜蛾成虫喙管感器的类型、分布和形态特征及其感器神经元在脑部的投射形态,为深入了解小菜蛾喙管感器的生理和功能奠定了基础。     

External anatomy of adult antennal sensilla of the fly,Trichopoda pennipes F. (Diptera: Tachinidae)

Antennae of both sexes of the feather-legged fly, Trichopoda pennipes F. (Diptera : Tachinidae) are described based on SEM observation. Socketed bristles and microtrichia were found on scape and pedicel, while a large number of different types of sensilla, interpersed with numerous microtrichia, were present on the entire surface of the 3rd antennal segment (funiculus). Seven types of sensilla, at least 3 of them olfactory, were observed and classified on the basis of external anatomical characteristics, such as shape, pore presence and density. A single deep pit, containing groups of sensilla, was present in both sexes on the lateral side of the funiculus.     

Antennal sensilla of Magicicada cassini (fisher) (Homoptera : Cicadidae): Fine structure and electrophysiological evidence for olfaction

The antennae of Magicicada cassini (Homoptera : Cicadidae) (3–4 mm long) look similar in both sexes and consist of scape, pedicel, and a 5-segmented flagellum. The length of flagellar segment 1 varies independently in relation to head size and is slightly longer in females (0.96 mm) than in males (0.89 mm). The ventral side of flagellar segment 1 is covered with sensilla coeloconica comprising about 60 large, 10 medium-sized, and 35 small sensilla with pit diameters of 8–24, 6–10, and 2 μm, respectively. The large and the medium-sized sensilla coeloconica are multiporous single-walled sensilla with pore tubules, containing branched entangled dendrites from 3 receptor cells. The small sensilla coeloconica, situated primarily at the outer border of the sensillum field, are no-pore sensilla with inflexible sockets. They contain 2 unbranched dendrites extending to the tip of the peg, and 1 dendrite reaching to its base and wrapping around the other 2 dendrites. Small sensilla campaniformia (cap diameter 3 μm) are aligned at the outer border of the sensillum field and continue all along the flagellum. Up to 3 olfactory receptor cells were distinguished on the basis of their nerve impulse amplitudes through extracellular electrophysiological recordings from sensilla coeloconica, presumably large ones. They respond to stimulation by cyclic terpenoids with different but highly overlapping reaction spectra, and react selectively to structural variations of the molecules. No responses to CO₂, temperature or moisture were recorded.     

Sexually dimorphic antennal structures of New Zealand Cave Wētā (Orthoptera: Rhaphidophoridae)

Insect antennae carry diverse sensory organs for detecting information about their environments and facilitating interaction among individuals, particularly for reproductive behaviour. As such they are predicted to be sexually dimorphic, especially in species which do not use visual or auditory mate-location. The cave wētā are such animals, suggesting that they rely heavily on chemical and tactile information to interact. Sensilla morphology and sexual dimorphism was investigated in two species; Pachyrhamma acanthocera and P. waitomoensis, using scanning electron microscopy. Fourteen types of sensilla basiconica, campaniformia, chaetica, coeloconica, trichodea and Böhm’s sensilla were identified. Among these, sexual dimorphism in the length of four subtypes was detected, and surprisingly, P. waitomoensis males completely lacked all but two of the porous sensilla types. In addition, three types of unique horn-like and hooked antennal protrusions in male P. acanthocera are described, along with similar, but less diverse structures on the antennae of male P. waitomoensis.     

Olfactory sensilla on the antenna and maxillary palp of the sheep head fly,Hydrotaea irritans (Fallen) (Diptera : Muscidae)

Antennae and maxillary palps of both sexes of the Sheep Head fly Hydrotaea irritans (Diptera : Muscidae) were investigated using scanning electron microscopy to describe the types, morphology, and distribution of olfactory sensory structures. Only socketed bristles and microtrichia were found on the scape of the antennae. These structures were also observed on the pedicel together with a group of 7–8 as yet undescribed sensilla, whose function is unknown. Olfactory sensilla were not found on these 2 segments or on the arista. Large numbers of olfactory sensilla and microtrichia were present on the funiculus. The former included sensilla trichodea (thick-walled, multiporous sensilla), sensilla styloconica and 6 types of sensilla basiconica (thin-walled, multiporous sensilla), 4 of which occurred individually and 2 of which were found in groups. An olfactory pit containing groups of thin-walled multiporous sensilla was located on the dorsomedian side of the funiculus. All sensilla basiconica were classified on morphological characteristics. The maxillary palps were covered with microtrichia and socketed bristles, but only 1 type of olfactory sensillum was found. This was a type of sensillum basiconicum that differed from any of those found on the antennae. No differences were found in sensilla diversity and distribution between males and females.     

Les pieces buccales et leurs recepteurs sensoriels chez l'imago de Micropterix calthella L. (Lepidoptera : Micropterigidae)

The aim of our study is to describe the mouthparts of Micropterix calthella (Lepidoptera) and their sensilla by the scanning electron microscope (SEM). The imaginal mouthparts are primitive. They are well adapted for collecting and grinding pollen of Ranunculus flowers. The maxillary palps show specialized structures for collecting pollen: mushroom-shaped hairs and blade-like structures. The brushes on the epipharynx, the teeth on the mandibles and the triturating basket on the hypopharynx grind the pollen to powder before absorption.Sensilla of different types have been observed on the mouthparts. The labrum, galeae, laciniae, and labial palps possess sensilla chaetica. Epipharynx, galeae, laciniae, and hypopharynx show sensilla basiconica. Sensilla trichoidea have been observed on the laciniae and sensilla campaniformia on the maxillary palps and the hypopharynx. At the top of each maxillary palp is a perforated area of unknown function. Two cavities are present at the distal extremity of each labial palp: one with sensilla coeloconica and the other with a perforated heart-shaped organ. The mushroom-shaped hairs, the blade-like structures, and the perforated heart-shaped organs have not yet been described in other insects.     

Ultrastructure of the labial tip sensilla of the tarnished plant bug,Lygus lineolaris (P. de Beauvois) (Hemiptera : Miridae)

Sensilla on the labial tip of the tarnished plant bug, Lygus lineolaris, were examined with scanning and transmission electron microscopy in order to provide morphological evidence indicative of their function. The tripartate apex of the labium consists of 2 lateral lobes and an apical plate. Each lateral lobe possesses a field of 11 thick-walled, uniporous peg sensilla, 5–6 μm long and a thick-walled, nonporous hair sensillum, 18–22 μm long. The uniporous peg sensilla are innervated by 3 or 5 bipolar neurons. The nonporous hair sensillum has no dendrites within its lumen. The apical plate is a noninnervated structure which possesses terminal cuticular projections 5–8 μm long. Morphological evidence supports previously reported physiological evidence that the uniporous peg sensilla have a chemosensory function.     

烟盲蝽成虫触角感器的扫描电镜观察

烟盲蝽Nesidiocoris tenuis(Reuter)作为一种杂食性昆虫,是蔬菜害虫的重要捕食者。利用扫描电镜对烟盲蝽雌雄成虫的触角进行观察,结果表明:烟盲蝽触角由基节、柄节、梗节和鞭节组成。绝大部分触角感器位于触角的腹面和外侧面。触角感器共有9种,分别为毛形感器、刺形感器、锥形感器、钟形感器、腔锥形感器、具弯钩形感器、腔形感器、乳形感器和Bhm氏鬃毛。腔锥形感器仅见于雌性触角,其他8种感器在雌雄两性触角上的类型和分布没有明显的区别。     

Labial tip sensilla of Blissus leucopterus leucopterus (Hemiptera: Blissidae): Ultrastructure and behavior

The cuticular sensory receptors that are found on the apex of the labium of hemipterans play an important role in their feeding behavior. In this study we describe the ultrastructure, number, and distribution of sensilla on the labium apex of the chinch bug, Blissus leucopterus leucopterus. Each apical field of sensilla on the labium contains 11 uniporous peg sensilla and one sensillum chaeticum. The uniporous peg sensilla are innervated by 4–5 bipolar neurons that send dendrites in the lumen of each peg. Three neurons are associated with each sensillum chaeticum, two neurons have dendrites in the lumen of the sensillum, and the third dendrite ends in a tubular body at the base of the sensillum. Behavioral tests that involve chemical blockage of the sensory receptors show the importance of the labial sensilla in feeding behavior. Both morphological and behavioral evidence indicate that the labial sensilla have a chemosensitive function.     

Olfactory responses and sensilla morphology of the blackcurrant leaf midge Dasineura tetensi

Olfactory responses of Dasineura tetensi (Rubs) (Diptera; Cecidomyiidae) to leaf volatiles of blackcurrant (Ribes nigrum) were tested in a 4-way olfactometer. Newly emerged virgin females showed no response to the leaf volatiles emitted from a blackcurrant shoot. Newly emerged males (which are known to respond to a pheromone released by the female) also showed no response to the leaf volatiles. Two hours after mating females responded positively, indicating that leaf volatiles may play a role in host plant finding. Scanning (SEM) and transmission (TEM) electron microscopy of the antennae of D. tetensi showed that males and females share five sensillum types; sensilla chaetica (mechanoreceptors), sensilla trichodea, sensilla basiconica, uniporous peg sensilla and circumfila (chemoreceptors). The sensilla chaetica and sensilla trichodea resemble those found on other insects. Sensilla basiconica were found on all antennal subsegments except the tip. These are multiporous receptors with five unbranched dendrites filling the lumen. Small peg sensilla located on the tips of both male and female antennae may function as contact-chemoreceptors. The circumfila, which are a unique type of sensilla found only on cecidomyiid antennae, form loops around each of the antennal subsegments, being attached to the surface by a series of stalks. TEM revealed that each stalk consisted of one sensillum containing a single highly branched dendrite. The distal regions of the walls of each sensillum are fused together to form the circumfila. Circumfila have multiporous walls and a lumen filled with multiple branches of dendrites. Their structure suggests that they are important olfactory receptors in both the male and female.     

Morphology and distribution of sensilia on the cephalic appendages,tarsi and ovipositor of the European sunflower moth,Homoeosoma nebulella Den. & Schiff. (Lepidoptera : Pyralidae)

Sensilla on male and female antennae, mouthparts, tarsi and on the ovipositor of the European sunflower moth, Homoeosoma nebulella (Lepidoptera : Pyralidae) have been investigated by means of scanning electron microscope. The antennal flagellum bears multiporous sensilla (trichodea, basiconica, auricillica, coeloconica) and uniporous sensilla (chaetica, styloconica). A sexual dimorphism is found in the numbers of sensilla trichodea (8300 in males and 6000 in females) and sensilla basiconica (1150 in females and 650 in males). The proboscis has uniporous s. styloconica, multiporous s. basiconica (described for the first time in Lepidoptera), aporous s. chaetica, and some rare uniporous s. basiconica in the food channel. The labial palp-pit organ houses multiporous s. coeloconica, while the maxillary palps have aporous sensilla. Tarsi of both sexes possess one type of aporous s. chaetica and 2 types of uniporous s. chaetica. There is no significant difference in the distribution of tarsal sensilla between males and females. The surface of each lobe of the ovipositor is covered by 3 types of aporous s. trichodea of different lengths and about 60 multiporous s. basiconica, sensilla unusual on the ovipositor of Lepidoptera. The role of sensilla in the oviposition site selection is discussed.