Diffusion barriers in silkmoth sensory epithelia: application of lanthanum tracer to olfactory sensilla of Antheraea polyphemus and Bombyx mori

The distribution of diffusion barriers in silkmoth olfactory sensilla has been investigated with ionic lanthanum. The tracer was applied from the apical side of the sensory epithelium by first pinching off the hair tips and then dipping the antennal branches into the La(NO(3))(3) solution. The tracer neither passed the apical septate junctions between the dendrite and the thecogen cell nor those between thecogen, trichogen, and tormogen cells, nor the tight contact between the apical membrane of the tormogen cell and the cuticle. After perfusing the hemolymph space with La(NO(3))(3) solution, the tracer was found in the clefts between the thecogen, trichogen, tormogen, and epidermis cells, but not in those between the receptor cells and the thecogen cell, or between the axon and the glial envelope. Lanthanum neither entered the receptor-lymph space nor the subcuticular space. Therefore, (i) receptor-lymph space, subcuticular space, and hemolymph space are isolated from each other, and (ii) the cleft between thecogen and sensory cell is separated from the hemolymph as well as from the receptor-lymph spaces. Furthermore, the results indicate that pleated septate junctions form the diffusion barriers in silkmoth olfactory sensilla.     

Volume and surface of receptor and auxiliary cells in hygro-/thermoreceptive sensilla of moths (Bombyx mori,Antheraea pernyi,and A. polyphemus)

Summary The thermo/hygroreceptive sensilla styloconica of the silkmoths Bombyx mori, Antheraea pernyi, and A. polyphemus were reconstructed from serial sections of cryofixed and chemically fixed specimens. The volume and surface area of the different sensillar cells were calculated from the area and circumference of consecutive section profiles. In addition, data are provided on the length and diameter of the outer and inner dendritic segments of the receptor cells. The morphometric data obtained from the three species are highly consistent and significantly different from those of olfactory sensilla trichodea of the same species. In each sensillum two type-1 receptor cells (hygroreceptors) are associated with one type-2 cell with a lamellated outer dendritic segment, a comparatively thick inner dendritic segment, and a particularly large soma (thermoreceptor). In contrast to olfactory sensilla, the thecogen cell is the largest auxiliary cell forming an extensive apical labyrinth bordering the inner sensillum-lymph space, whereas an inconspicuous trichogen cell and a medium-sized tormogen cell border a comparatively small outer sensillum-lymph cavity. Moreover, both sensillum-lymph spaces are separated from each other not only by the dendrite sheath, but also by the trichogen cell. The results are discussed with regard to recent electrophysiological observations and current hypotheses on the function of sensilla.     

Ultrastructure of the chemosensitive basiconic single-walled wall-pore sensilla on the antennae in adults and embryonic stages of Locusta migratoria L. (Insecta,Orthoptera)

Summary The structure and embryonic development of the two types (A, B) of basiconic sensilla on the antennae of Locusta migratoria were studied in material that had been cryofixed and freeze-substituted, or chemically fixed and dehydrated. Both types are single-walled wall-pore sensilla. Type-A sensilla comprise 20–30 sensory and 7 enveloping cells. One enveloping cell (thecogen cell secretes the dendrite sheath); four are trichogen cells, projections of which form the trichogen process during the 2nd embryonic molt. The trichogen cells form two concentric pairs proximally. Two tormogen cells secrete the cuticular socket of the sensillum. The dendritic outer segments of the sensory cells are branched. Bifurcate type-A sensilla have also been observed. Type-B sensilla comprise three sensory and four enveloping cells (one thecogen, two trichogen and one tormogen). The trichogen process is formed by the two trichogen cells, each of which gives rise to two projections. The trichogen cells are concentrically arranged. The dendritic outer segments of the sensory cells are unbranched. In the fully developed sensillum, all trichogen and tormogen cells border on the outer receptor lymph cavity. It is suggested that the multicellular organization of the type-A sensilla can be regarded as being advanced rather than primitive.Supported by the Dcutschc Forschungsgemeinschaft (SFB 4/G1)     

Pheromone receptors in Bombyx mori and Antheraea pernyi

Summary The cellular organization of freeze-substituted antennal sensilla trichodea, which contain the sex pheromone receptors, was studied in male silkmoths of two species (Bombyx mori, Bombycidae; Antheraea pernyi, Saturniidae). The cellular architecture of these sensilla is complex, but very similar in both species. A three-dimensional reconstruction of a sensillum trichodeum of B. mori is presented. Two receptor cells (in A. pernyi 1–3) and three auxiliary cells are present. Of the latter, only the thecogen cell forms a true sheath around the receptor cells. A unique thecogen-receptor cell junction extends over the entire area of contact. Septate junctions occur between all sensillar cells apically, and in the region of the axonal origin basally. Gap junctions are also found between all cells except the receptor cells. The trichogen and tormogen cells show many structural indications of secretory activity and are thought to secrete the receptor lymph. Their apical membrane bordering the receptor-lymph space is enlarged by microvilli and microlamellae, but only those of the trichogen cell show regularly arranged membrane particles (portasomes), indicating secretory specialization among the auxiliary cells. Epidermal cells are found as slender pillars between sensilla, but extend apically along the non-sensillar cuticle and basally along the basal lamina.     

Ultrastructure and ontogeny of the hair sensilla on the funicle of Calliphora erythrocephala (Insecta,Diptera)

Summary Four envelope cells are responsible for the formation of the basiconical sensilla of Calliphora. They are the thecogen, trichogen, and tormogen cells, and envelope cell 4. In early stages of development the still subepithelial sensory cilia are completely enclosed by the innermost thecogen cell. The first formation movements are initiated by a growth thrust of the hair-forming cell into the exuvial space. The sensory cilia only begin to grow into the hair anlage when the hair-forming cell has almost reached its final length. As soon as growth is completed the trichogen cell, tormogen cell, and envelope cell 4 start to excrete cuticular material. The trichogen cell forms the perforated part of the hair shaft and the stimulus-conducting system consisting of the pore tubules. The tormogen cell is responsible for the excretion of the basal non-perforated hair shaft and sheath cell 4 forms the proximal part of the socket region. The thecogen cell only begin to produce dendritic sheath material when the sensory hair is almost complete.Approximately 7–8 days after pupation the tormogen cell degenerates, having, by this time, produced about two-thirds of the sensilla cuticle. The surrounding envelope cells incorporate cell fragments of the tormogen cell. The trichogen cell continues the secretion where the tormogen cell left off. When the secretion of cuticle is finished the sheath cells begin to withdraw towards the proximal direction and to form microvilli on the apical membrane. The resulting outer receptor lymph space is bordered by envelope cell 4 and the trichogen and thecogen cells. The tormogen cell is absent in the sensilla of the imago.Abbreviations DS dendritic sheath - E4 envelope cell 4 - Ex exuvial space - G glial cell - iD inner dendritic segment - iRL inner receptor lymph space - oRL outer receptor lymph space - oD outer dendritic segment - P pore - PT pore tubules - S sensory cell - T thecogen cell - TO tormogen cell - TR trichogen cell Part 1 of a dissertation accepted by the Faculty of Bio- and Geosciences, University of Karlsruhe     

Differentiation of the thermo-/hygrosensitive (no-pore) sensilla on the antenna of Antheraea pernyi (Lepidoptera,Saturniidae): a study of cryofixed material

Summary The morphogenesis of the thermo- and hygro-sensitive sensilla styloconica of Antheraea pernyi was studied, exclusively by cryomethods, during the second half of pupal development. The three major processes taking place during this period are (1) the differentiation of the dendritic outer segments of the sensory cells, especially of the lamellated type-2 receptor, (2) the formation of the receptor-lymph cavities, (3) the formation of tubular structures of unknown function in the inner receptor-lymph cavity, and (4) the elongation of the dendrite sheath. The formation of lamellae in the type-2 dendritic outer segment is achieved by the enfolding of its originally cylindrical cytoplasmic membrane. Autocellular junctions, previously described in the sensilla of adult animals, are found to join the forming lamellae. Close similarities between the junctions and smooth septate junctions are demonstrated. Both the extensive inner and outer receptor-lymph cavities are formed by invagination and folding of the apical cytoplasmic membranes of the three enveloping cells. Formation starts at the most apical projection of the cells and proceeds in a proximal direction. Up to 4-m-long tubular structures appear, exclusively in developmental stages, in the inner receptor-lymph cavity. They are composed of plasma membranes whose inner surface is studded with regularly spaced electron-dense particles. Contacts with the cytoplasmic membrane of the innermost enveloping cell demonstrate that the structures are composed of lipid membranes. During elongation of the dendrite sheath, which in these sensilla is apically attached to the hair wall, an 2-m-long growth-zone is observed at its proximal end. By addition of sheath-forming material to the growth-zone, the latter continuously moves proximally until the sheath is completed.     

The structure of the terminal sensilla on the maxillary palps of Locusta migratoria (L.), and changes associated with moulting

Summary The basic structure of the terminal sensilla of Locusta migratoria resembles that of Schistocerca gregaria. There are commonly six or ten neurons whose dendrites extend almost to the opening of the peg. Proximally the dendrites are clothed by a neurilemma cell which also encloses a basal cavity through which their ciliary region passes. The tormogen cell encloses the receptor-lymph cavity and actively secretes material into it. The receptor-lymph cavity and the basal cavity are quite separate.The development of new pegs at a moult is described. After apolysis the scolopale extends across the subcuticular space and protects the dendrites, which remain in a functional condition until shortly before ecdysis. As the trichogen cell grows out to form a new peg the tip is surrounded by a mass of electron-dense material, probably derived from the receptorlymph cavity. The function of this material is unknown. Regeneration of the dendrites is considered.The possible mechanism by which the tip of the peg opens and closes is considered and the general structure of the organule is discussed in relation to functioning.     

Very tight contact of tormogen cell membrane and sensillum cuticle: ultrastructural basis for high electrical resistance between receptor-lymph and subcuticular spaces in silkmoth olfactory hairs

A very tight contact is present between the apical membrane of the tormogen cell and the cuticle of the hair base in olfactory sensilla trichodea of Antheraea polyphemus. The contact zone is characterized by numerous hemidesmosome-like structures of the cell membrane, which closely attach the latter to the cuticle. If apically opened hairs are incubated in a LaCl3 solution, the tracer ions do not penetrate the contact zone. It is concluded that the tight contacts are the morphological correlates of the electrical isolation of the receptor-lymph space (cf. de Kramer et al., in press).     

Ultrastructure and receptor cell responses of the antennal grooved peg sensilla of Triatoma infestans (Hemiptera: Reduviidae)

Ultrastructural examination of grooved-peg (GP) sensilla on the antenna of fifth instar Triatoma infestans nymphs by scanning electron microscopy and transmission electron microscopy reveal that they are 8–18 μm long with a diameter of about 2–2.8 μm at the non-articulated base. Some pegs have a terminal pore. These double-walled wall-pore (dw-wp) sensilla have an outer cuticular wall with 13–18 longitudinal grooves at the distal part of the peg. Groove channels are present at the bottom of the grooves from which radial spoke channels lead into the inner sensillum-lymph cavity. A dendrite sheath connects the tip of the thecogen cell to the inner cuticular wall thus forming separated outer and inner sensillum-lymph cavities. Four or five bipolar receptor cells are ensheathed successively within the GP sensilla by the thecogen cell, trichogen and tormogen cells. The inner dendritic segments of each sensory cell give rise at the ciliary constriction to an unbranched outer dendritic segment which can reach the tip of the sensillum.Electrophysiological recordings from the GP sensilla indicate that they house NH₃, short-chain carboxylic acid and short-chain aliphatic amine receptor cells and can be divided into three functional sub-types (GP 1–3). All GP sensilla carry a receptor cell excited by aliphatic amines, such as isobutylamine, a compound associated with vertebrate odour. GP type 1 and 2 sensilla house, in addition, an NH₃-excited cell whereas the type 2 sensilla also contains a short-chain carboxylic acid receptor. No cell particularly sensitive to either NH₃ or carboxylic acids was found in the grooved-peg type 3 sensilla. GP types 1, 2 and 3 represent ca. 36, 10 and 43% of the GP sensilla, respectively, whereas the remaining 11% contain receptor cells that manifest normal spontaneous activity but do not respond to any of the afore mentioned stimuli.     

Atlas of olfactory organs of Drosophila melanogaster 2. Internal organization and cellular architecture of olfactory sensilla

Antennae and maxillary palps of Drosophila melanogaster were studied with the electron microscope on serial sections of cryofixed specimens. The number of epidermal cells roughly equals the number of sensilla, except for regions where the latter are scarce or absent. Each epidermal cell forms about two non-innervated spinules, a prominent subcuticular space and a conspicuous basal labyrinth, suggesting a high rate of fluid transport through the sensory epithelium. The internal organization and fine structure of trichoid, intermediate and basiconic sensilla is very similar. Receptor cell somata are invested by thin glial sheaths extending distad to the inner dendritic segments. Further distally, the thecogen cell forms a sleeve around the dendrites, but an extracellular dendrite sheath is absent. At the base of the cuticular apparatus, the inner sensillum-lymph space around the ciliary and outer dendritic segments is confluent with the large outer sensillum-lymph space formed by the trichogen and tormogen cells. All three auxiliary cells exhibit many features of secretory and transport cells but extend only thin basal processes towards the haemolymph sinus. The bauplan and fine structure of coeloconic sensilla differs in the following aspects: (1) the ciliary segment of the dendrites is located deeper below the base of the cuticular apparatus than in the other sensillum types; (2) a prominent dendrite sheath is always present, separating inner and outer sensillum-lymph spaces completely; (3) the apical microlamellae of the auxiliary cells are more elaborate, but free sensillum-lymph spaces are almost absent; (4) there are always four not three auxiliary cells. Morphometric data are presented on the diameter of inner and outer dendritic segments and on the size of receptor cells, as well as of the receptor and auxiliary cell nuclei. The special fine structural features of Drosophila olfactory sensilla are discussed under the aspects of sensillar function and the localization of proteins relevant for stimulus transduction.     

Structure of isolated sensilla and sensory neurons in vitro: Observations on developing silkmoth antennae

Summary By combined enzymatic and mechanical treatment, it was possible to dissociate the sensory epithelium of developing antennae of male Antheraea polyphemus and A. pernyi silkmoths from the stage of separation of the antennal branches up to the early stages of cuticle deposition. Large numbers of entire developing trichoid sensilla were isolated. These are characterized by a large trichogen cell with a long apical, hair-forming process and a large nucleus. A cluster of 2–3 sensory neurons, enclosed by the thecogen cell, is situated in the basal region. The dendrites run past the nucleus of the trichogen cell into the apical process from which they protrude laterally. The nuclei of the tormogen and a 4^th enveloping cell can be distinguished near the base of the prospective hair. After further dissociation, only the neuron clusters remain, still enclosed by their thecogen cell and often attached to the antennal branch nerve via their axons. It is finally possible to disrupt the thecogen cells and the axons, leaving the sensory neurons with inner dendritic segments and axon stumps. The majority of these neurons can be expected to be olfactory.     

Cellular organization of the dome sensillum: A presumed chemoreceptor in Gammarus setosus (Gammaridea: Amphipoda)

A previously unknown type of sensillum with a thin cuticular dome and two pairs of pores is described in the amphipod Gammarus setosus. There is only one dome sensillum on each interantennal lobe of the head. The receptor is innervated by two sensory dendrites that bifurcate into two pairs of 9 + 0 cilia, concentrically enclosed by four auxiliary cells—two thecogen, one trichogen, and one tormogen and surrounded by a cluster of accessory cells. The ciliary regions are contained in small inner lymph cavities. The outer segments are sheathed by the apical extensions of the thecogen cells, are looped inside the outer lymph cavity, and come in close contact with lipid spheroids inside the dome. The basal bodies consist of microtubule doublets, which extend into the distal segments where they are interspersed with singlets. The nodal inner dendritic segments join the ventral suspension cord of the organ of Bellonci and enter its ganglion. The application of colloidal lanthanum resulted in intraciliary lanthanum deposits. The dome sensilla are presumed to be chemosensory because their cellular plan has similarities to that of some known olfactory and pheromone-sensitive sensilla in decapod crustaceans and insects. © 1994 Wiley-Liss, Inc.     

Immunocytochemical localization of pheromone-binding protein in moth antennae

Summary Odorant-binding proteins are supposed to play an important role in stimulus transport and/or inactivation in olfactory sense organs. In an attempt to precisely localize pheromone-binding protein in the antenna of moths, post-embedding immunocytochemistry was performed using an antiserum against purified pheromone-binding protein of Antheraea polyphemus. In immunoblots of antennal homogenates, the antiserum reacted exclusively with pheromone-binding protein of A. polyphemus, and cross-reacted with homologous proteins of Bombyx mori and Autographa gamma. On sections of antennae of male A. polyphemus and B. mori, exclusively the pheromone-sensitive sensilla trichodea are labelled; in A. gamma, label is restricted to a subpopulation of morphologically similar sensilla trichodea, which indicates that not all pheromone-sensitive sensilla contain the same type of pheromone-binding protein and accounts for a higher specificity of pheromone-binding protein than hitherto assumed. Within the sensilla trichodea, the extracellular sensillum lymph of the hair lumen and of the sensillum-lymph cavities is heavily labelled. Intracellular label is mainly found in the trichogen and tormogen cells: in endoplasmic reticulum, Golgi apparatus, and a variety of dense granules. Endocytotic pits and vesicles, multivesicular bodies and lysosome-like structures are also labelled and can be observed not only in these cells, but also in the thcogen cell and in the receptor cells. Cell membranes are not labelled except the border between thecogen cell and receptor cell and the autojunction of the thecogen cell. The intracellular distribution of label indicates that pheromone-binding protein is synthesized in the tormogen and trichogen cell along typical pathways of protein secretion, whereas its turnover and decomposition does not appear to be restricted to these cells but may also occur in the thecogen and receptor cells. The immunocytochemical findings are discussed with respect to current concepts of the function of pheromone-binding protein.     

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 the sensilla of Peripatopsis moseleyi (Onychophora)

Summary Three types of sensilla occurring on the lips and on the antennae of Peripatopsis moseleyi have been investigated by scanning and transmission electron microscopy. On the lips sensory spines can be found which contain numerous cilia originating from bipolar receptor cells. They reach the tip of the spine where the cuticle is modified. The perikarya of the sensory cells, a large supporting cell with a complicated surface and a second type of receptor, form a bud-like structure and are surrounded by a layer of collagen fibrils. The second receptor cell bears apical stereocilia as well as a kinocilium which are directed towards the centre of the animal — thus the cell appears to be turned upside down. The sensilla of the antennae are 1) sensory bristles containing two or three kinds of receptor cells, one of which bears an apical cilium and one kind of supportive cell and 2) sensory bulbs located within furrows consisting of receptor cells with branched cilia and two kinds of supportive cells which are covered by a modified thin cuticle. According to the electron microscopical findings the sensory spines on the lips are presumably chemoreceptors. The sensory bristles on the antennae can be regarded as mechanoreceptors and the sensory bulbs as chemoreceptors.Supported by the Deutsche Forschungsgemeinschaft (Sto 75/3)     

The fine structure of thermo-/hygrosensitive sensilla in the silkmoth Bombyx mori: Receptor membrane substructure and sensory cell contacts

Summary The thermo-/hygroreceptive sensilla styloconica of the silkmoth Bombyx mori are located on the tips of the antennal branches. A small poreless cuticular peg is innervated by three sensory cells. The outer dendritic segments of two type-1 receptor cells, the presumed hygroreceptors, almost completely fill the peg lumen and are in close contact with each other. The outer dendritic segment of the third (type-2) receptor cell, the presumed thermoreceptor, forms lamellae below the peg base. The membranes of these lamellae are studded with knobs in orthogonal array, protruding into the extracellular space with the same orientation on facing lamellae. This Bossy Orthogonal Surface Substructure (BOSS) is assumed to play a role in thermoreceptor function. Contacts are observed between the outer dendritic segments, between the inner dendritic segments immediately below the ciliary segments, and between the sensory cell somata. These contacts, which are not found in the olfactory sensilla (s. trichodea and basiconica) of this species, indicate electrical interactions between the three sensory cells of the styloconic sensillum and possibly are involved in the antagonistic and/or bimodal response characteristics of thermo-/hygroreceptor cells.     

Analysis of immunocytochemical staining patterns in the antennal system of Drosophila melanogaster

By immunizing mice with homogenized brains, heads, or a mixture of heads and antennae of D. melanogaster, we obtained six monoclonal antibodies (mabs) that bind to the olfactory system of Drosophila with various degrees of specificity. They can be divided into three groups with respect to their staining pattern: (1) The antibodies ca51/2, na21/2, and nb230 label both in the third (olfactory) antennal segment and in the visual ganglia. All of them bind to antennal structures that can be correlated with basiconic sensilla. The antibody ca51/2 labels sensory neurons of these sensilla. In the antenna of the lozenge ³ mutant, which lacks basiconic sensilla, no labeling is present. In Western blots ca51/2 recognizes in the antenna an antigen of 43.5 kDa, which is expressed in the antenna only in the presence of basiconic sensilla. The antibody na21/2 binds to basiconic and coeloconic sensilla, most likely to the apical part of sheath cells. In immunoblots it recognizes in the antenna two antigens of 42.2 kDa and 46.7 kDa. The latter appears to be correlated in the antenna with the presence of basiconic sensilla. (2) The staining pattern of antibody nc10 is associated with the sheath cells of basiconic and coeloconic sensilla. Moreover, nc10 binds to a subset of glomeruli in the antennal lobe. (3) The staining pattern of the antibodies VG2 and I24B5 is restricted to the antenna. I24B5 recognizes coeloconic sensilla and VG2 recognizes both coeloconic and basiconic sensilla. Staining patterns in both cases include sheath cells.     

Ultrastructure des sensilles trochanteriens de Campodea sensillifera conde et mathieu (Diplura : Campodeidea)

The fine structure of the basiconica sensilla situated on the posterior part of trochanters in Campodea sensillifera (Diplura : Campodeidea) reveals that they are probably olfactory and mechano-sensitive setae. Each sensillum is composed of one sensory axis made of 3 dendrites ensheathed by 3 cells (thecogen, trichogen and tormogen); one outer segment ends by a tubular corper without connection with the cuticular layer. The setae are generally racket-shaped. The epicuticular layer of the expanded part is perforated by a lattice of numerous slits, which communicate with underlying canals. The ciliary structures and apex of the tormogen cell are eliminated just before ecdysis. The ciliary microtubules are present in the cavity of the new sensillum, but after ecdysis the microtubules persist only at the lower part of the peduncle. An ecdysial canal appears at the tip of the sensillum.     

Die digitiformen Sensillen auf dem Maxillarpalpus von Coleoptera

Summary The digitiform sensilla on the distal segment of the maxillar palps ofAgabus bipustulatus (L.) andHydrobius fuscipes (L.) were investigated by electron microscopic methods. Each sensillum is innervated by a single bipolar sensory cell. The sensilla ofHydrobius are associated with three enveloping cells, which enclose an inner and outer receptor lymph cavity. A single enveloping cell only is found in the completely differentiated sensilla ofAgabus. These sensilla do not form an outer lymph cavity. The area beneath the hair base is filled by the distal process of the enveloping cell and by extensions of epidermal cells. Only one extra-cellular space exists, which seems to be homologous to an inner receptor lymph cavity.The outer dendritic segment surrounded by a dendritic sheath runs to the tip of the hair shaft. In the hair shaft the outer dendritic segment divides into several branches. The poreless hair shaft does not rise over the surface of the cuticle, but it is positioned in a narrow shallow groove. Special socket structures or a tubular body do not exist. The digiti-form sensilla possess neither the typical feature of mechanosensitive, nor gustatory or olfactory sensilla. The functional significance of the structural divergences in the sensilla of both species and the presumed function of the sensilla are discussed referring to hygro- and thermo-receptors.

Unserem verehrten Lehrer, Herrn Prof. Dr. H.Risler, dem wir für vielfache Förderung danken möchten, zum 65. Geburtstag gewidmet.     

The cercal sensilla of the blowfly Lucilia cuprina. II. Structure of the enveloping cells and the basal regions of the sensory dendrites

The gustatory, olfactory, touch and stress receptors on the cerci of Lucilia cuprina Wied. (Diptera: Calliphoridae) have either two or three enveloping cells. The gustatory and olfactory sensilla have three enveloping cells: a tormogen, trichogen and thecogen cell. The tormogen and trichogen cells contribute to a sub-cuticular sensillar lumen which divides into two lobes basally. The thecogen cell forms a lumen around the dendrites. Distally the dendrites lie in the contents of the thecogen lumen within the dendritic sheath. Proximally the dendrites embed in the thecogen cell which has an expanded, microlamellate lumen basally. The sensillar lumen of the mechanosensory (trichoid mechanoreceptors and campaniform) sensilla is formed by a single enveloping cell: the presumptive tormogen cell. In trichoid mechanoreceptors the thecogen lumen is restricted to the region of the transitional region of the dendrite whereas the thecogen lumen of campaniform sensilla extends proximally although it is not as well-developed as that of the chemoreceptive sensilla. The dendrites of all sensillum types on the cerci have a granular body in the transitional region: a situation which has not been previously reported in chemoreceptive sensilla although common in the mechanoreceptors of Calliphoridae and Sarcophagidae.