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.     

Structure of galeal sensory complex in adults of the red turnip beetle,Entomoscelis americana brown (Coleoptera,Chrysomelidae)

Summary The internal and external structure of the galeae of the adult red turnip beetle, Entomoscelis americana, was studied using SEM and TEM. The galea broadens from base to truncated tip and its sides are of thick, sculpted cuticle invested with pores and coarse spines. The tip is of thinner, flexible cuticle covered with 8–12 uniporous, blunt-tipped apical pegs and a single, aporous, sharply-pointed apical hair.The coarse spines are singly innervated probable mechanosensilla owing to the tubular body at the distal end of the dendrite. These sensilla likely act as tactile hairs monitoring galeal-effected movements of food particles into the functional mouth. The pores are associated with glands within the galea. The function of the presumed secretion is not known but may be to keep objects and dried saliva from sticking to the mouthparts.The apical pegs are innervated by five neurons, each producing a single dendrite. Four dendrites enter the single peg lumen and communicate with the terminal pore. The fifth differentiates into a tubular body that inserts into the peg base. These are typical insect contact chemosensilla that, because of their location, would taste incoming food.The apical hair has no pores but is innervated by two neurons, each extending a dendrite into the hair lumen in chemosensillar fashion. The sensory mode of this sensillum is unknown but is probably not mechanoor chemoreception. Many of its features, reminiscent of taste hairs, lead us to hypothesize that it represents a one-time chemosensillum recently modified to a new form and sensory mode.Because larval and adult E. americana share similar food plant requirements, we hypothesize that similarities will be seen in their mouthpart sensilla. Comparisons of the adults and larvae show the common features between their respective galeal taste hairs are only those of insect contact chemosensilla in general. However, the adult apical hair and the larval medial sensillum show striking specific structural similarities. We propose that these are true structural and functional homologues.     

Mapping and ultrastructure of antennal chemosensilla of the wheat bug Eurygaster maura

Antennae of the wheat stink bug Eurygaster maura L. (Hemiptera: Scutelleridae) were investigated to elucidate structure and distribution of antennal chemosensilla in females. Five type of sensilla were identified and characterized using a scanning electron microscope (SEM) and a transmission electron microscope (TEM). Type 1 sensilla are mechanical and contact chemoreceptors with a single apical pore. Types 2 and 3 sensilla are multiporous chemoreceptors both with typical features of olfactory sensilla. Type 4 are multiporous peg-like sensilla, short and with a grooved surface. Type 5 are sensilla coeloconica with a smooth and aporous peg completely inserted in a sub-cuticular chamber. All types are distributed on the two flagellar segments, but we considered only the apical flagellomere in which the largest number of sensilla are located. The most abundant sensilla are type 3, while the less numerous are type 5. All types, except type 2, decreased in number from the tip to the base of the segment. The lower density of sensilla was recorded on the dorsal-internal part of the apical antennomere, while the higher density was recorded on the opposite side (external-ventral).     

Fine structure of the antennal sensilla of the millipede Orthomorphella pekuensis (Polydesmida: Paradoxosomatidae)

The fine structural characteristics of various sensory receptors on the antenna of a millipede, Orthomorphella pekuensis, were observed with field emission scanning electron microscopy. The antenna of this millipede has eight segments, called articles. On the surface of the antenna, there are a variety of sensory receptors, including olfactory and mechanical receptors. According to their morphological and fine structural characteristics, we could identify four basic types of antennal sensillum: chaetiform sensilla (CS), trichoid sensilla (TS), basiconic sensilla (BS) and apical cone sensilla (AS). The BS are divided further into three subtypes: large basiconic sensilla (BS₁) on the 5th and 6th articles; small basiconic sensilla (BS₂) on the 5th article; and a distinct type of basiconic spiniform sensilla (BS₃) on the 7th article. The most prominent sensilla are four large AS on the distal tip of the 8th segment. Based on our results, we conclude that the main function of the CS and TS are related to mechanical reception, and that the BS and AS are likely to function in olfactory reception of volatile odors of plants, as these sensilla have base and apex pores, respectively.     

Sensilla on the maxillary palps of Helicoverpa armigera caterpillars: in search of the CO(2)-receptor

The ultrastructure of sensilla on the maxillary palps of helicoverpa armigera caterpillars has been investigated in order ot find candidates for CO(2)-receptors. The following sensilla are found on the palps: a) 8 chemosensory pegs at the tip; b), a large distal pore plate; c), a smaller proximal pore plate; d), a digitiform organ; e), a campaniform sensillum; and f), 3 scolopidia. Each chemosensory peg at the tip is innervated by 4-5 sensory neurons. Five of these pegs are most probably contact chemoreceptors, because each has a dendrite with a tubular body. The distal pore plate has a porous cuticle and is innervated by 3 sensory neurons, each of which sends a highly branched dendrite into a large cuticular cavity. The proximal pore plate is made up from two fused organs, has also a porous cuticle, and is innervated by two sensory neurons which send their dendrites into a narrow cuticular channel. The digitiform organ is innervated by one sensory cell which sends a highly lamellated dendrite into a narrow channel within a chip-shaped protrusion of the porous cuticle. For several reasons, the digitiform organ is the most probable candidate for the CO(2)-receptor. Another possible candidate is the distal pore plate.     

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。     

Fine-structural characteristics of the antennal sensilla of Agrotis segetum (Insecta: Lepidoptera)

Summary The turnip moth Agrotis segetum possesses seven different types of sensilla: four single-walled (SW), one double-walled (DW), one terminal-pore (TP), and one poreless sensilla (NP).The SW 1 and SW 2 sensilla have the same external appearance, being long and slender, but differ in the branching pattern of the sensory processes: unbranched and branched in SW 1 and SW 2, respectively. The SW 3 sensilla are shorter, sickle-shaped, and contain a large number of branches from the sensory processes. These three sensillar types are innervated by 2–3 sensory cells. The SW 4 sensilla are raisin-shaped and possess three profusely branched sensory processes. The DW sensilla are short and have apical slit-like pores. This sensillar type has 5–6 sensory processes. The TP sensilla possess five sensory processes, one of them terminates basally in a tubular body, the others in the apical part of the long cuticular bristle. The NP sensilla are stout and have apical conelike structures. Two of the sensory processes terminate in the apical part, the third proximally. The third sensory process has a lamellar pattern. The fine structure indicates the following functions: SW and DW sensilla: chemoreception; TP sensillum: chemoreception and mechanoreception; NP sensillum: thermoreception and hygroreception.Supported by joint grants from the Swedish Council for Planning and Coordination of Research, the Swedish Natural Science Research Council, and the Swedish Council for Forestry and Agricultural Research     

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.     

Antennal chemoreceptors of the desert burrowing cockroach, Arenivaga sp

The antennae of Arenivaga have six types of chemoreceptor sensilla. Some of these have unusual morphological features which may be adaptations for survival in a dry habitat. The sensory dendrites are well protected by cuticular structures, and in some receptors stimulatory molecules must pass through long channels or through pores filled with strands to reach the sensory cells. Large grooved pegs (possibly pheromone receptors) are numerous on antennae of adult males, and grooved sensilla are described here in detail for the first time. Thin-walled pegs, present in males and females, do not have pore tubules or hollow filaments as observed in many other insects. Rather, they contain structures designated here as pore strands, since they have a dense core rather than a light center as previously described for pore tubules and filaments. These strands do not appear to be evaginations of the dendritec membrane, but are probably formed in association with the cuticular structures of the sensilla.     

Morphology and distribution of antennal sensilla of the tarnished plant bug,Lygus lineolaris (Palisot de beauvois) (Hemiptera: Miridae)

Sensilla on the antennae of adult and last-instar nymphs of the tarnished plant bug, Lygus lineolaris (Hemiptera: Miridae), were examined with light, scanning and transmission electron microscopy. Six different types were identified in adult females and males and 5 types in last-instar nymphs: types 1 and 4 are sensilla trichodea, 2 and 3 are sensilla chaetica, and 5 and 6 are sensilla basiconica. Type 1 are located at distal region of terminal segment and type 2 are located at distal regions of proximal 3 segments in both adults and nymphs. Type 3 is present on all segments, more numerous on scape and pedicel and less abundant on distal third and fourth segments in both adult and nymphal stages. Types 4 and 6 are absent on the scape and present on the distal 3 antennal segments in adults, but they are present only on the distal-most antennal segment in nymphs. Type 5 sensilla are present only on second antennal segments in adults and are absent in nymphs. Sexual dimorphism is observed in total numbers: there are significantly more type(s) 3, 4, 5 and 6 sensilla in adult males than adult females. Types 1, 4 and 5 are multiporous with thin cuticle, branched dendrites and pore tubules which suggests an olfactory function. These sensilla have 3, 3 and 2 neurons, respectively. The type 6 sensillum has an apical pore and pores in the cuticular wall, and is innervated by 5 nerve cells with unbranched dendrites. Sensillar types 2 and 3 have thick cuticle, a single apical pore and nerve cells with unbranched dendrites. Type 2 has 1 neuron and type 3 has 2 chambers and 2 nerve cells.     

Ultrastructure of sensilla on the antennal pedicel of the brown planthopper Nilaparvata lugens Stal (Insecta: Homoptera)

Scanning- and transmission electron-microscope studies of the sensilla of the pedicel of Nilaparvata lugens have revealed an elaborate plaque organ and three structurally different types of trichoid hairs. Each plaque organ is innervated by 120-150 neurons arranged in groups. The porous sensory cuticle is folded into finger-like projections and is surrounded by protective non-sensory denticles. Trichoid sensilla differ in number of neurons, appearance of dendrites and arrangement of pores. Type I, innervated by 2 neurons, has pores along its length and is probably olfactory in function. Types II and III are innervated by one and five neurons, respectively, and the absence of pores along the hair shaft indicates a possible gustatory role. The importance of these sensilla is discussed with reference to the behaviour of this important insect pest.     

Ultrastructure and physiology of the CO2 sensitive sensillum ampullaceum in the leaf-cutting ant Atta sexdens

The sensilla ampullacea on the apical antennomere of the leaf-cutting ant Atta sexdens were investigated regarding both their responses to CO2 and their ultrastructure. By staining the sensillum during recording, we confirmed that the sensilla ampullacea are responsible for CO2 perception. We showed that the sensory neurons of the sensilla ampullacea are continuously active without adaptation during stimulation with CO2 (test duration: 1 h). This feature should enable ants to assess the absolute CO2 concentration inside their nests. Sensilla ampullacea have been found grouped mainly on the dorso-lateral side of the distal antennal segment. Scanning and transmission electron microscopic investigations revealed that the external pore opens into a chamber which connects to the ampulla via a cuticular duct. We propose protection against evaporation as a possible function of the duct. The ampulla houses a peg which is almost as long as the ampulla and shows cuticular ridges on the external wall. The ridges are separated by furrows with cuticular pores. The peg is innervated by only one sensory neuron with a large soma. Its outer dendritic segment is enveloped by a dendritic sheath up to the middle of the peg. From the middle to the tip numerous dendritic branches (up to 100) completely fill the distal half of the peg. This is the first report of a receptor cell with highly branched dendrites and which probably is tuned to CO2 exclusively.     

Fine structure of the galeal styloconic sensilla of larval Lymantria dispar (Lepidoptera: Lymantriidae)

Lepidopteran larvae possess two pairs of styloconic sensilla located on the maxillary galea. These sensilla, namely the lateral and medial styloconic sensilla, are each comprised of a smaller cone, which is inserted into a style. They are thought to play an important role in host-plant selection and are the main organs involved in feeding. Ultrastructural examination of these sensilla of fifth instar Lymantria dispar (L.) larvae reveal that they are each approximately 70 um in length and 30 um in width. Each sensillum consists of a single sensory peg inserted into the socket of a large style. Each peg bears a slightly subapical terminal pore averaging 317 nm in lateral and 179 nm in medial sensilla. Each sensillum houses five bipolar neurons. The proximal dendritic segment of each neuron gives rise to an unbranched distal dendritic segment. Four of these dendrites terminate near the tip of the sensillum below the pore and bear ultrastructural features consistent with contact chemosensilla. The fifth distal dendrite terminates near the base of the peg and bears ultrastructural features consistent with mechanosensilla. Thus, these sensilla each bear a bimodal chemo-mechanosensory function. The distal dendrites lie within the dendritic channel and are enclosed by a dendritic sheath. The intermediate and outer sheath cells enclose a large sensillar sinus, whereas the smaller ciliary sinus is enclosed by the inner cell. The neurons are ensheathed successively by the inner, intermediate, and outer sheath cells.     

The role of pore structures in the selective permeability of antennal sensilla of the desert burrowing cockroach, Arenivaga sp

To obtain information about the chemical composition of pore structures in antennal sensilla, the antennae were exposed to lipid solvents, or they were prepared to show negative-contrast images in electron micrographs. A heavy-metal tracer, lanthanum nitrate, was also used to indicate the permeability of the receptors to water. The grooves of the large grooved peg open into tubular cavities containing electronopaque material, through which stimulatory molecules must pass to reach the sensory dendrites at the center of the sensillum. The material in these cavities was removed by chloroform or acetone, suggesting a lipid composition. Lanthanum penetrated this receptor only after it had been exposed to acetone or chloroform. Strands at pores of the thin-walled pegs were also removed by the lipid solvents, and the water-soluble tracer failed to penetrate these receptors unless they had been previously exposed to chloroform or acetone. The pore structures appear to be hydrophobic, allowing entry of lipid-soluble substances, while preventing passage of water. The differential action of the solvents on the various types of sensilla suggests that receptor discrimination among different classes of chemical stimuli may be partially determined by the chemical properties of structures at the sensillar pores.     

Antennal sensilla and their possible functions in the host-plant selection behaviour of Phenacoccus manihoti (Matile-Ferrero) (Homoptera : Pseudococcidae)

Nine different types of sensilla have been identified on the antenna of the cassava mealybug Phenacoccus manihoti (Homoptera : Pseudococcidae) with scanning and transmission electron microscopes. Trichoid sensilla, distributed on all segments of the antenna and innervated by a single mechanoreceptive dendrite, have the characteristics of exteroceptors. A campaniform sensillum located on the pedicel and one basiconic sensillum on the flagellum have the characteristics of proprioceptors. Coeloconic sensilla, located ventrally on the pedicel and flagellum, related to poreless sensilla with inflexible sockets, have the characteristics of thermo/hygroreceptors. Uniporous sensilla with a mechanoreceptive dendrite (smooth pegs P1 and P2, grooved pegs P3) and multiporous chemosensilla (grooved pegs P4 and P5), present on the tip of the flagellum, have, respectively, the characteristics of gustatory and olfactory receptors. The results of this study seem to suggest that the cassava mealybug has sensory equipment on its antennae that can detect, by olfaction and contact, chemicals released by the plant.     

疟疾媒介中华按蚊触角感器的扫描电镜观察

【目的】明确中华按蚊Anopheles sinensis雌成虫与幼虫触角感器的类型、形态和分布。【方法】利用光学显微镜观察中华按蚊成虫与幼虫触角的形态结构,利用扫描电镜观察触角上的感器类型、形态和分布。【结果】中华按蚊雌成虫触角由柄节、梗节和鞭节组成,鞭节有13个亚节。触角上共发现4种类型的感器,分别为毛形感器(锐型和钝型)、刺形感器(大型和小型)、锥形感器(Ⅰ型和Ⅱ型)和腔锥形感器(大型和小型)。雌成虫触角各类感器总计约1 135.67±86.75个,其中毛形感器数量最多(662.00±6.22个),随后是刺形感器(294.67±33.35个)和锥形感器(146.00±42.39个),腔锥形感器数量最少(36.50±5.90个)。毛形感器、刺形感器和锥形感器在鞭节的每个亚节均有分布,而大型腔锥形感器在第9-11亚节没有分布,小型腔锥形感器仅分布于第13节的顶端。幼虫触角的鞭节不分亚节,呈管状,触角末端有一个感觉锥,鞭节上分布有与成虫锥形感器相似的锥形凸起,初步定名为类锥形感器,其数量和大小随幼虫龄期的增长而显著增加,锥体表面的凹槽越来越明显,其功能还需要通过超微结构和电生理等研究进一步确定。【结论】本研究对中华按蚊幼虫和雌成虫触角感器的形态特征、类型、数量及其分布进行了观察和分析,结果为进一步研究中华按蚊感器的生理功能奠定了基础。     

Ultrastructure of the funicular sensilla of the cabbage root fly,Delia radicum L. (Diptera : Anthomyiidae)

A transmission electron microscope study of the funicular sensilla of the cabbage root fly, Delia radicum, (Diptera : Anthomyiidae), showed 4 types of surface sensilla and 5 types of pit sensilla. The ultrastructure of the surface sensilla indicated all had a primary olfactory function. These include thick-walled multiporous trichoid sensilla, thin-walled multiporous basiconic sensilla (with 2 subtypes), thin-walled multiporous clavate sensilla, and grooved sensilla with channels at the base of each of the grooves. Clavate sensilla had 2 types of dendrites, one tubular, the other “scrolled”. This 2nd type may indicate an additional thermosensitive function. The dorsal pits contained thin-walled multiporous basiconic sensilla with a tapered tip. The ventral pits contain 3 types of sensilla, which have no wall pores and an inflexible socket. These may contain thermo- and/or hygroreceptors and include smooth-walled conical-, smooth-walled tapered- and striated pit sensilla. The 4th type is a grooved pit sensillum similar to the surface type.     

Fine structure and primary sensory projections of sensilla located in the sacculus of the antenna of Drosophila melanogaster

Sensilla lining the inner walls of the sacculus on the third antennal segment of Drosophila melanogaster were studied by light and transmission electron microscopy. The sacculus consists of three chambers: I, II and III. Inside each chamber morphologically distinct groups of sensilla having inflexible sockets were observed. Chamber I contains no-pore sensilla basiconica (np-SB). The lumen of all np-SB are innervated by two neurons, both resembling hygroreceptors. However, a few np-SB contain one additional neuron, presumed to be thermoreceptive. Chamber II houses no-pore sensilla coeloconica (np-SC). All np-SC are innervated by three neurons. The outer dendritic segments of two of these neurons fit tightly to the wall of the lumen and resemble hygroreceptor neurons. A third, more electron-dense sensory neuron, terminates at the base of the sensillum and resembles a thermoreceptor cell. Chamber III of the sacculus is divided into ventral and dorsal compartments, each housing morphologically distinct grooved sensilla (GS). The ventral compartment contains thick GS₁, and the dorsal compartment has slender sensilla GS₂. Ultrastructurally, both GS₁ and GS₂ are doublewalled sensilla with a longitudinal slit-channel system and are innervated by two neurons. The dendritic outer segment of one ofthe two neurons innervates the lumen of the GS and branches. On morphological criteria, we infer this neuron to be olfactory. The other sensory neuron is probably thermoreceptive. Thus, the sacculus in Drosophila has sensilla that are predominantly involved in hygroreception, thermoreception, and olfaction. We have traced the sensory projections of the neurons innervating the sacculus sensilla of chamber III using cobaltous lysine or ethanolic cobalt (II) chloride. The fibres project to the antennal lobes, and at least four glomeruli (VM₃, DA₃ and DL_2-3) are projection areas of sensory neurons from these sensilla. glomerulus DL₂ is a common target for the afferent fibres of the surface sensilla coeloconica and GS, whereas the VM₃, DA₃ and DL₃ glomeruli receive sensory fibres only from the GS.     

Sensory organs of the antennae and mouthparts of beetle larvae (Coleoptera)

The sensilla located on the antennae and maxillary and labial palps of the larvae of 64 beetle species from 22 families were studied using electron microscopy. The larvae of beetles living in different habitats and having different trophic specializations possess a uniform structure of the sensory organs. They are composed of two groups of sensilla on the apical and subapical segments of the antennae, one apical group of sensilla on both maxillary and labial palps, and one or several digitiform sensilla on the lateral surface of the maxillary and, occasionally, labial palp. The external morphology of the sensory organs is adaptive and represents modifications of the initial type. Band-shaped sensilla or placoid sensilla, clearly different from the initial sensory organs, appear in some taxa as rare exceptions, while other groups display either partial reduction of the receptor organs (Gyrinidae) or reduction of the cuticular parts of the sensilla (Cantharidae).     

Fine structure and distribution of antennal sensilla of the desert locust, Schistocerca gregaria (Orthoptera: Acrididae)

The fine structure and distribution of various types of antennal sensilla in three nymphal stages and in adults of both solitary-reared (solitary) and crowd-reared (gregarious) phases of the desert locust, Schistocerca gregaria, were investigated by scanning and transmission electron microscopy. Four types of sensilla were identified: sensilla basiconica, s. trichodea, s. coeloconica and s. chaetica. S. basiconica contain up to 50 sensory neurons, each of which displays massive dendritic branching. The sensillar wall is penetrated by a large number of pores. In contrast, s. trichodea contain one to three sensory neurons that branch to give five or six dendrites in the sensillar lumen; the sensillum wall is penetrated by relatively few pores. The s. coeloconica are situated in spherical cuticular pits on the antennal surface. The s. coeloconica are of two types: one type contains one to three sensory neurons with double sensillar walls penetrated by slit-like pores, whereas the second type contains four sensory neurons with non-porous double sensillar walls. The s. chaetica have a flexible socket and a thick non-porous sensillum wall and contain four sensory neurons that send unbranched dendrites to a terminal pore. A fifth sensory neuron of the s. chaetica terminates in a tubular body at the base of the hair. S. basiconica and coeloconica are normally distributed over the entire antennal flagellum, with a concentration in the middle segments; s. trichodea have three areas of concentration on the 5th, 10th and 14th flagellar segments. Sensilla chaetica are most abundant on the terminal segment. Locusts raised in solitary conditions have more olfactory sensilla (s. basiconica and s. coeloconica) than crowd-reared locusts. The difference in sensillar numbers is more evident in adults than in nymphs. These results suggest that differences in the odour-mediated behaviour of nymphs and adults, and between the phases of S. gregaria, may be attributable to differences at the sensory input level.