Distribution of olfactory and some other antennal sensilla in the male click beetle Agriotes obscurus L. (Coleoptera : Elateridae)

The distribution of 5 types of sensilla was statistically analysed on the 4–10th antennal segments of the male click beetle Agriotes obscurus (Coleoptera : Elateridae). The distribution pattern of the trichoid pheromone receptors (T₂ sensilla) and the olfactory basiconic B₁B₂ sensilla on the antennae of male A. obscurus differs significantly from the distribution pattern of the contact chemoreceptors (T₁ sensilla) and probably the non-olfactory B₇ and D sensilla. A significant peculiarity of the distribution of olfactory sensilla is their location on the antennal segments as 2 separate (dorsal and ventral) fields of sensilla. The numbers of T₂ and B₁B₂ sensilla on dorsal fields of sensilla of the 4–10th segments increase towards the apex of the antenna nearly linearly. On ventral fields of sensilla of the 4–10th antennal segments, the number of B₁B₂ sensilla is nearly uniform; the number of T₂ sensilla in the proximal part of the antenna increases towards the apex, but on distal segments of the antenna their number stabilizes. It is characteristic of both the T₂ and to B₁B₂ sensilla that their numbers are slightly greater on anterior than posterior sides of dorsal sensillar fields, and also greater on posterior than anterior sides of ventral sensillar fields of all antennal segments investigated. We assume that the number of olfactory sensilla on the antennae of male beetles coincides with the distribution of strength of olfactory signal on the antennae of beetles orientating in an odour plume. The distribution patterns of T₂ and B₁B₂ sensilla of the male A. obscurus can be related to some behavioural peculiarities of olfactory orientation (walking or flying and vibrating of the antennae).     

Antennal sensilla of the click beetle,limonius aeruginosus (OLIVIER) (COLEOPTERA: ELATERIDAE)

Antennal sensilla typology, number and distribution of the click beetle Limonius aeruginosus (Olivier) (Coleoptera: Elateridae) were studied using scanning electron microscopy. The serrate antennae of both sexes of L. aeruginosus consist of the scape, pedicel and of the flagellum which is composed of 9 flagellomeres. In both sexes, 5 types of sensilla basiconica, 1 type of sensilla trichodea, 1 type of sensilla chaetica, 1 type of sensilla campaniformia and Böhm sensilla were distinguished. No remarkable sexual differences in the types, numbers and distribution of sensilla were found on the antennae, except for the sensilla basiconica type II. The average number of sensilla basiconica type II on the antennae of the male beetle surpassed that on the antennae of the female beetle (3562 and 108 pegs, respectively). It is suggested that this type of sensilla on the male beetles antennae is responsible for the reception of the sex pheromone produced by the female beetle.     

Morphological and ultrastructural characterization of olfactory sensilla in Drosophila suzukii: Scanning and transmission electron microscopy

Drosophila suzukii is a serious horticultural and quarantine pest, damaging various berry crops. Although the active use of olfactory communication in D. suzukii is well-known, their olfactory sensory system has not been comprehensively reported. Therefore, the present study was carried out to understand the morphology, distribution and ultrastructure of olfactory sensilla present in the antennae and maxillary palps of D. suzukii, through scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The olfactory sensilla on the antennae of D. suzukii in both sexes could be classified into three major morphological types, basiconic, trichoid and coeloconic sensilla, according to their shapes. The antennal basiconic sensilla were further divided into three subtypes and the antennal trichoid sensilla into two subtypes, respectively, according to the size of individual sensillum. In contrast to the antennal olfactory sensilla showing diverse morphology, basiconic sensilla was the only type of olfactory sensilla in the maxillary palps of D. suzukii. The basiconic sensilla in the maxillary palps could be further classified into three subtypes, based on their size. Our SEM and TEM observations indicated that multiple nanoscale pores are present on the surface of all types of olfactory sensilla in the antennae and maxillary palps, except coeloconic sensilla. The difference in the morphological types and the distribution of olfactory sensilla suggests that their olfactory functions are different between antennae and maxillary palps in D. suzukii. The results of this study provide useful information for further studies to determine the function of olfactory sensilla in D. suzukii and to understand their chemical communication system.     

Morphological characterization of the antennal sensilla of t he earwig Anisolabis maritima (Dermaptera: Carcinophoridae) with reference to their probable functions

The earwig, Anisolabis maritima (Dermaptera: Carcinophoridae), is one of the most significant insects in KSA because, it was recorded in Saudi Arabia as a beneficial predator on eggs and newly hatched larvae of the red palm weevil, Rhyncophorus ferrugineus. We examined the external morphology of the antennal sensilla of males and females of A. maritima using scanning electron microscopy (SEM). The filiform antennae of A. maritima were of the conventional type comprising a basal scape, pedicle and a long, thread-like flagellum, which was composed of 12 flagellomeres of males and 16 flagellomeres of females. Six morphologically unique sensillar types were found and described on the antennae of males and females of A. maritima. Of those identified, there were three types of porous trichoid sensilla (long, curved and arcuate), and two types of basiconic sensilla (short and curved), and one type of aporous trichoid sensilla. The shape, external morphology and array of sensilla on the antennae of males and females of A. maritima were similar.     

Morphological and functional heterogeneity in olfactory perception between antennae and maxillary palps in the pumpkin fruit fly,Bactrocera depressa

The morphology and ultrastructure of the olfactory sensilla on the antennae and maxillary palps were investigated through scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and their responses to five volatile compounds were measured using electroantenogram (EAG) and electropalpogram (EPG) techniques in the pumpkin fruit fly, Bactrocera depressa (Shiraki; Diptera: Tephritidae). Male and female B. depressa displayed distinct morphological types of olfactory sensilla in the antennae and maxillary palps, with predominant populations of trichoid, basiconic, and coeloconic sensilla. Basiconic sensilla, the most abundant type of olfactory sensilla in the antennae, could be further classified into two different types. In contrast, the maxillary palps exhibited predominant populations of a single type of curved basiconic sensilla. High‐resolution SEM observation revealed the presence of multiple nanoscale wall‐pores on the cuticular surface of trichoid and basiconic sensilla, indicating that their primary function is olfactory. In contrast, coeloconic sensilla displayed several longitudinal grooves around the sensillum peg. The TEM observation of individual antennal olfactory sensilla indicates that the basiconic sensilla are thin‐walled, while the trichoid sensilla are thick‐walled. The profile of EAG responses of male B. depressa was different from their EPG response profile, indicating that the olfactory function of maxillary palps is different from that of antennae in this species. The structural and functional variation in the olfactory sensilla between antennae and maxillary palps suggests that each plays an independent role in the perception of olfactory signals in B. depressa.     

Morphology and ultrastructure of the chemosensory sensilla of larval antennae in the Colorado potato beetle, Leptinotarsa decemlineata Say (Coleoptera: Chrysomelidae)

The allocation, external morphology, and ultrastructure of various types of sensilla on the antennae have been studied in the larvae of the Colorado potato beetle (Leptinotarsa decemlineata Say) using scanning and transmission electron microscopy. It has been found that the larval antenna bears 11 sensilla of four morphological types: trichoid (five), basiconic (four), styloconic (one), and antennal cone (one). It has been shown that the sensilla are innervated by 2?C7 receptor cells: trichoid, by 2?C4 receptor cells; basiconic, by 4?C7 receptor cells; and styloconic, by 6 receptor cells. Judging by the specifics of their ultrastructural organization, the function of these sensilla is gustatory. The antennal cone is innervated by two receptor cells, and its function is olfactory.     

Morphology and untrastructure of the antennal sense organs in tenebrionid larvae <Emphasis Type="Italic">Tenebrio molitor</Emphasis> L. and <Emphasis Type="Italic">Zophobas rugipes</Emphasis> Kirsch (Coleoptera: Tenebrionidae)

The distribution, external morphology, and ultrastructure of various types of sensilla in the antennae of tenebrionid larvae Tenebrio molitor and Zophobas rugipes are studied by means of scanning and transmission electron microscopy. On the antennae of T. molitor there are sensilla of four basic morphological types: basiconic, styloconic, trichoid, and papillate sensilla. On the antennae of Z. rugipes, in addition to the aforementioned ones, there are placoid sensilla. Ultrastructure points to olfactory function of basiconic and placoid sensilla. Other sensillum types are contact chemoreceptors.     

Scanning Electron Microscopy Studies of the Antennal Sensilla of Metaphycus parasaissetiae Zhang & Huang (Hymenoptera: Encyrtidae)

Metaphycus parasaissetiae Zhang & Huang (Hymenoptera: Encyrtidae) is an important adult parasitoid of Parasaissetia nigra Nietner (Hemiptera: Coccoidea). The external morphology of the antennal sensilla of male and female M. parasaissetiae was examined using scanning electron microscopy. The geniculate antennae of male and female M. parasaissetiae were composed of a scape with a basal radicula, a barrel-shaped pedicel, and a long flagellum. Twelve morphologically distinct types of sensilla were identified, including multiporous placoid sensilla, campaniform sensilla, finger-like sensilla, multiporous basiconic sensilla (BS-1), three aporous types of basiconic sensilla (BS-2, BS-3, and BS-4), two types of aporous trichoid sensilla (TS-1 and TS-3), a type of multiporous trichoid sensilla (TS-2), and two types of sensilla chaetica (CH-1 and CH-2). Sex dimorphism in the sensilla composition of M. parasaissetiae is also observed. Major differences between the sexes were found in the number, distribution, shape, structure, and size of the identified sensilla. We also discuss on the functional aspects of these sensilla to elucidate the mechanisms involved in host searching and courtship behavior of M. parasaissetiae.     

伪鞘榕小蜂雌雄成虫触角感器的超微形态、分布及适生意义

伪鞘榕小蜂Sycoscapter trifemmensis是一种寄生于鸡嗉子榕间花期榕果的专性寄生蜂,雌雄两性繁殖策略分化明显,为更好理解和诠释雌蜂寄主定位和雄蜂配偶识别机制,有必要对两性的触角感器进行观察。运用环境扫描电镜观察,对比和探讨了伪鞘榕小蜂雌雄成虫的触角和触角感器类型、分布、数量及其生态适应性。结果表明:雌蜂触角鞭节由11鞭小节组成,总长817.82±33.23μm,分布有毛形感器、刺形感器(类型1)、锥形感器(类型1)、多孔板形感器(类型1)、栓锥形乳突状感器5类5种;雄蜂触角鞭节仅由6鞭小节组成,全长为雌蜂的1/3,且各节有明显的缩短和增粗特征,着生感器包括毛形感器、刺形感器(类型2和类型3)、锥形感器(类型1和类型2)、多孔板形感器(类型2)、腔锥形感器5类7种。雌蜂触角感器的数量与分布显著高于雄蜂,且同类型感器在雌蜂上具有明显的延伸、增粗、分支的特征,以板形感器和锥形感器最为突出。伪鞘榕小蜂雌雄成虫的触角及其感器有明显的性二型,特别是与化学信息识别相关的感器,反映了雌雄蜂在不同生态环境和繁殖压力下的形态分化、行为策略和生态适应。     

Antennal sensilla of the ground beetle Bembidion lampros Hbst (Coleoptera, Carabidae)

Antennal sensilla typology, number and distribution pattern were studied in the ground beetle Bembidion lampros Hbst (Coleoptera, Carabidae) using scanning electron microscopy. The 1.6–1.8 mm long filiform antennae of both sexes consist of the scape, pedicel and of the flagellum composed of nine flagellomeres. In both sexes, three types of sensilla chaetica, two types of sensilla trichodea, five types of sensilla basiconica, one type of sensilla coeloconica, one type of sensilla campaniformia and Böhm sensilla were distinguished. The possible function of the sensilla was discussed and three types of sensilla were considered as olfactory, sensilla trichodea type 2 and sensilla basiconica types 1 and 2. Olfactory sensilla occupy dorsal and/or ventral areas of the flagellomeres and occur sparsely (sensilla basiconica type 1) or not at all (sensilla basiconica type 2 and sensilla trichodea type 2) outside these areas. No remarkable sexual differences in the types, numbers and distribution of antennal sensilla were found.     

Comparison of antennal sensilla of Anaphes victus and A. listronoti (Hymenoptera, Mymaridae), egg parasitoids of Curculionidae

Antennal sensilla were compared in females and males of two sympatric mymarid Hymenoptera, Anaphes victus and A. listronoti which are, respectively, solitary and gregarious parasitoids of eggs of the carrot weevil Listronotus oregonensis (Coleoptera, Curculionidae). Both species are morphologically very similar in the area where they are sympatric. The external morphology of the sensilla was studied using scanning electron microscopy. Female antennae have seven different types of sensilla, morphologically similar in the two species: trichoid sensilla, which are putative mechanosensilla, sensilla chaetica types 1, 3 and 4, which are presumably contact chemosensilla, and sensilla chaetica type 2 and basiconic and placoid sensilla, which are presumed to be olfactory sensilla. The major difference between the two species is the number of sensilla chaetica type 4, of which 6–9 are found on the antennal club in A. victus, while 10–12 are present in A. listronoti. The antennae of the males of both species are similar in morphology and in the number and distribution of their four types of sensilla, i.e. trichoid sensilla, sensilla chaetica type 1 and basiconic and placoid sensilla. Accepted: 23 November 1998     

Sensilla on the mouthparts and antennae of the elephant louse,Haematomyzus elephantis piaget (Phthiraptera: Haematomyzidae)

The labial palpus of the elephant louse Haematomyzus elephantis has six sensilla that represent three different types: trichoid, basiconic, and styloconic. Two rows of basiconic sensilla are situated on the dorsal and ventral surfaces of the rostrum, and each row consists of three sensilla. Male and female antennae have 15–17 trichoid sensilla situated on the scape, pedicel, and three antennal annuli. Both sexes have two sensilla basiconica on the dorsal surface of the pedicel near the junction of the scape and pedicel. Two coeloconic (tuft) sensilla are situated on the antennae of both sexes, one sensillum on each of the last two annuli. There are three plate organs, two on the last annulus and one on the penultimate annulus of the male and female antennae. Sexual dimorphism is exhibited in the male and female antennae, in that the male has about twice as many sensilla basiconica on the apex of the last annulus as does the female. The total number of sensilla basiconica on the apex of the male antennae is at least two times the number that is known to be present in any other species of lice. © 1992 Wiley-Liss, Inc.     

Comparison of the antennal sensilla of females of four fig-wasps associated with Ficus auriculata

A comparison was performed of the antennal sensilla of females of four chalcid wasp species Ceratosolen emarginatus Mayr, 1906, Sycophaga sp., Philotrypesis longicaudata Mayr, 1906, and Sycoscapter roxburghi Joseph, 1957, which are specific and obligatory associated with Ficus auriculata (Lour, 1790). The four species exhibit different oviposition strategies in the fig ovules where their offspring hatch and develop. Antennal sensilla morphology was evaluated using scanning electron microscopy. Females of the four species present 11 morphologically similar types of sensilla: trichoid sensilla, sensilla obscura, chaetica sensilla 1 and 2, which all have mechanosensory functions; uniporous basiconic sensilla, which are presumably contact chemosensilla; basiconic capitate peg sensilla, coeloconic sensilla 1, multiporous basiconic and placoid sensilla, which may be regarded as olfactory sensilla, and coeloconic sensilla 2 and 3, which are presumed to be proprioreceptors or pressure receptors. The four species have significant differences in the abundance and arrangement of trichoid sensilla and chaetica sensilla 1 on the flagellum. The coeloconic sensilla and sensilla obscura only occur on the antennae of C. emarginatus that enter figs. The chemosensilla which are presumably involved in host discrimination, i.e., basiconic sensilla, multiporous placoid sensilla and basiconic capitate peg sensilla, are similar in shape and configuration, although they present some differences in abundance. These findings provide practical information on the adaptations of fig wasps and the relationship between multisensory antennae and functions in fig wasp behaviour.     

Antennal olfactory sensilla of the parasitoid fly,Pseudoperichaeta nigrolineata Walker (Diptera : Tachinidae)

The antennal sensilla of male and female Pseudoperichaeta nigrolineata Walker (Diptera: Tachinidae) were studied by scanning electron microscopy. Five types of sensilla were identified on the funicle. The trichoid sensilla are most conspicuous, with a characteristic distal curvature and wall pores. Basiconic types I and II sensilla show a small peg with a pitted surface. Basiconic type III sensilla can be distinguished from the preceding ones by the swelling of the distal region of the peg. The function of these sensilla is likely to be olfactory. Coeloconic sensilla consist of a short grooved peg sunk in a socket. The number and distribution of the sensilla of each type are described. Female antennae bear more basiconic sensilla than those of males. These results are compared with previously published studies on other muscoid species.     

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.     

Mate recognition and antennal morphology of Octodonta nipae (Coleoptera: Chrysomelidae) adults

The nipa palm hispid beetle, Octodonta nipae (Maulik) has been killing palm trees since its introduction into Hainan province, China, from Malaysia in 2001. It continues to spread within Hainan province, northeast to Fujian province, and northwest to Yunnan province within China. Knowledge on signals involved in mate location and recognition could help develop effective integrated pest management programs. In the present study, we first experimentally proved that antennae were essential in success of O. nipae mating. We then excised various segments/flagellomeres of adult male and female antennae and observed their mating behavior. Results revealed that the 5th to 9th flagellomeres, especially those of males, were important for the mating success. Finally, in an attempt to elucidate the types of antennal sensilla accountable for the mating success, morphology of O. nipae antennae was studied in detail with scanning electron microscopy. Six types of sensilla were distinguished: aporous sensilla trichodea (T1), multiporous sensilla trichodea (T2), aporous sensilla chaetica (Ch1), uniporous sensilla chaetica (Ch2), multiporous sensilla basiconica (B), and Böhm sensilla (Bm). Aporous sensilla trichodea is the most abundant; multiporous sensilla trichodea and sensilla basiconica are considered as olfactory receptors, and uniporous sensilla chaetica as gustatory receptor. Importance of flagellomeres 5–9 in mating success seemed to correspond to the abundance of sensilla on these segments.     

Antennal and ovipositor sensilla of Pseudoligosita yasumatsui (Hymenoptera: Trichogrammatidae)

Pseudoligosita yasumatsui Viggiani and Subba Rao 1978 (Hymenoptera: Trichogrammatidae) is a common egg parasitoid of rice insect pests. The surface morphology of the antenna and ovipositor on P. yasumatsui was examined using scanning electron microscopy. The antenna of P. yasumatsui is geniculate in shape, hinged at the scape-pedicel joint, approximately 190 μm in length and consists of seven antennomeres. In total, the male and female antennae have ten different types of sensilla: trichoid sensilla type 1, 2, 3, 4, 5, 6, campaniform sensilla, basiconic sensilla, and placoid sensilla type 1 and 2. The flagellum of the female antenna is covered with cuticular pores, which are absent on the male antennal flagellum. The distal extremity of its ovipositor stylet has campaniform sensilla and styloconic sensilla. Trichoid sensilla found on its apical abdomen part may play a role in the host detection and egg placement. The types and distribution of antennal and ovipositor sensilla on the parasitoid were discussed.     

The antennal sensilla of the praying mantis Tenodera aridifolia: A new flagellar partition based on the antennal macro-, micro- and ultrastructures

In insects, the antenna consists of a scapus, a pedicellus, and a flagellum comprising many segments (flagellomeres). These segments possess many morphological types of sensory organs (sensilla) to process multimodal sensory information. We observed the sensilla on flagellomeres in praying mantis (Tenodera aridifolia) with both scanning and transmission electron microscopes. We classified the sensilla into six types: chaetic, campaniform, coelocapitular, basiconic, trichoid and grooved peg sensilla, and inferred their presumptive functions on the basis of their external and internal structures. In addition, based on their distribution, we newly divided the flagellum into 6 distinct parts. This new division leads to a better understanding about the sexual dimorphism and the antennal development in the mantises. The sexual difference in distribution of the grooved peg sensilla suggests that this type of sensilla may play a role in sex-pheromone detection in mantis, which is a rare case of double-walled sensilla mediating this function.     

Antennal sensilla and sexual dimorphism of the adult ladybird beetle Semiadalia undecimnotata Schn. (Coleoptera: Coccinellidae)

The antennal receptors of the adult male and female ladybird beetle, Semiadalia undecimnotata (Coleoptera: Coccinellidae), were examined by scanning and transmission electron microscopy. Twelve types of receptors were characterized and grouped into 5 morphological classes: Böhm, trichoid, coeloconic, basiconic, and chetiform sensilla. Sensory function was determined on the basis of sensillar ultrastructure and electrophysiological response. Olfactory sensilla are confined in both sexes to the 2 terminal antennal segments. In contrast, gustatory and mechanosensitive organs are present along the entire length of the antennae. Sexual dimorphism of antennal receptors is limited to the latter 2 functional classes. The principal characteristics of this dimorphism are the following: a) males possess 540 sensilla (all types), while females possess only 500; b) males exhibit 2 types of taste receptors not present in females; c) females exhibit one type of mechanoreceptor absent in males; d) the 3 sex-specific types of sensilla, which occupy the same position in males and females, are confined to the inner side of the antennae. The possible role of male-specific sensilla in intersexual communication is discussed.     

Structure and function of antennal pore plate sensilla of oryctes rhinoceros (L.) (Coleoptera : Dynastidae)

The antennae of the rhinoceros beetle, Oryctes rhinoceros (Coleoptera : Dynastidae), comprise 4 parts : the scape, the pedicel, a funicle, and a club of 3 lamellate segments. The inner surfaces of the lamellate club segments carry one type of trichoid sensilla, 2 types of sensilla coeloconica, and 3 types of multiporous pore plate sensilla. The total surface occupied by the sensilla on the antenna is 5.2±0.4 mm² in males (mean±SD) and 5.4±0.5 mm² in females. With a measured density of 8665±1254 sensilla per mm² in males and 8952±1642 sensilla per mm² in females, the total number of pore plate sensilla was estimated to be between 45,000 and 50,000. The structure of the 3 types of pore plate sensilla is described. SP1 are the most abundant type of placoid sensilla. They show a convex and rugged plate whose infoldings form a circle of irregular cavities. SP2 sensilla are characterised by a smooth and convex plate, surrounded by a furrow with a ridge. SP2 are localised on a wide band situated along the straight side of the lamella. The plate of SP3 is nearly flat and there is no furrow. SP3 are confined within a narrow margin along the convex edge of lamellae. The 3 types of pore plate sensilla house 2 neurones whose dendrites branch repeatedly under a plate of thin (0.2 μm) cuticle, which is pitted with numerous pores, 40 nm in diameter. Single sensillum recordings with tungsten microelectrodes revealed the firing activity of 2 neurones. These receptor neurones responded specifically to olfactory stimulus. Olfactory receptor neurones tuned to the male pheromone compound, ethyl 4-methyl octanoate, were found in male and female antennae. Other receptor neurones responded to plant volatiles. Morphological and electrophysiological data suggest the absence of a sexual dimorphism in the olfactory organs. The functional organisation of the olfactory organs is discussed in terms of their adaptation to the ecology of O. rhinoceros.