Fine structure of the aesthetasc hairs ofPagurus hirsutiusculus dana

Summary The thin-walled aesthetasc pegs on the antennules of a small hermit crab,Pagurus hirsutiusculus, were studied by light and electron microscopy. The lumen of each aesthetasc was found to be filled with the dendrites of 300–500 bipolar neurons whose cell bodies lie beneath the base of the aesthetasc. These dendrites are ciliary in nature, having well developed basal bodies and rootlets.Each basal body gives rise to a cilium which divides to form a cluster of slender branches, each of which contains a microtubule running lengthwise. These structures occupy most of the length of the hair.The cuticle of the aesthetasc wall is thin and tenuous. Except for the pore canals in the basal region, we have found no pores at either light or electron microscope level, but as the hair is extremely permeable, we conclude that the cuticle itself may permit the passage of solutions. This permeability of the cuticle and the large numbers of dendrites within support the hypothesis that the aesthetascs are chemoreceptors.     

Structure of Aesthetascs in Selected Marine and Terrestrial Decapods: Chemoreceptor Morphology and Environment

We have compared the structure of the aesthetascs—thin-walledchemosensory pegs on the antennules—of Coenobita, a terrestrialhermit crab, and of various marine decapods, including the aquatichermit crab, Pagurus hirsutiusculus. In all cases, the aesthetascsare innervated by the dendrites of many bipolar neurons whosecell bodies are grouped beneath the bases of the hairs. Thedendrites have basal bodies and cilia that divide into slenderbranches, each distinguished by ovoid swellings along its lengthand containing one or more microtubules apparently continuouswith the microtubules of the cilia. The arrangement of the dendrites within the aesthetascs is distinctlydifferent in Coenobita from that in the marine animals, evenin its relative, Pagurus. There are many points of structuralconvergence between the aesthetascs of Coenobita and the thin-walledolfactory pegs of the insect antenna. These modifications mayrepresent adaptations for conservation of water in the terrestrialreceptors.     

A re-evaluation of the cytology of cat Pacinian corpuscles

Summary The aesthetascs of the spiny lobster, Panulirus argus, are hair sensilla located on the lateral filaments of the antennules. Each hair is about 0.8 mm long and innervated by about 320 bipolar sensory neurons, the dendrites of which project as a bundle into the hair shaft. Each of the dendrites develops two cilia. Within a very short distance each of these cilia branches repetitively and dichotomously resulting in 8000 to 10000 outer dendritic segments per hair, or about 20 to 30 branches per neuron. The branches intertwine frequently before running to the tip of the hair. Each hair also possesses inner and outer auxiliary cells. The inner auxiliary cells surround the bundle of dendrites, extending distally to the origin of the ciliary segments. Extensions of these cells project into the bundle of dendrites, separating groups of dendrites into discrete clusters. Outer auxiliary cells wrap the inner ones, but do not extend beyond the base of the hair.     

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.     

Fine structure and molting of aesthetasc sense organs on the antennules of the isopod,Asellus aquaticus (Crustacea)

In Asellus aquaticus certain distal antennular segments bear single sensilla referred to as aesthetascs. These show a proximal stem and a distal bulbous region. Depending on its position, each aesthetasc is innervated by either 50-60 or 70-80 bipolar sensory cells, the perikarya of which are situated within the pedunculus. Within the antennular segment the dendrites develop unbranched cilia (9 X 2 + 0 structure). The sensory cells are unusual in that mono- as well as biciliary dendrites are present within a single aesthetasc, the ratio of both types being correlated with the number of sensory cells. Cilia and receptor lymph cavity are enveloped by a set of 3-4 inner and 13-14 outer sheath cells, which terminate at the base of the sensillum, so that the delicate and poreless cuticle of the bulbous region encloses only outer segments within the receptor lymph fluid. A new molting type in arthropods is described in which the outer sheath cells alone build the new cuticle, whereas the inner sheath cells most probably have a protective function. A definition of aesthetascs is proposed based on fine-structural criteria. Functionally the sensilla are considered to be chemoreceptors. This assumption is confirmed by experiments with diluted vital dye as well as lanthanum showing that dissolved substances penetrate the poreless cuticle instantaneously.     

Innervation of the cercal sensilla on the ovipositor of the Australian sheep blowfly (Lucilia cuprina)

ABSTRACT. The ovipositor of the female sheep blowfly, Lucilia cuprina (Wied.) (Diptera: Calliphoridae), has a complement of cercal sensilla that includes long, medium and short tactile hairs, two campaniform domes, four olfactory pegs, and ten double-channelled gustatory hairs. This sensory array is suited to assess oviposition site resources, prior to and during the laying of an egg batch.
The tactile hairs and campaniform sensilla are each innervated by a single, tubular body containing dendrite. The olfactory pegs are each innervated by a single, moderately branched dendrite, which gains access to the external environment via pores at the bottom of deep grooves in the peg wall. The gustatory hairs fall into two categories. Four hairs have a single, tubular body containing dendrite at their base, and four unbranched dendrites running up to the hair tip which has a terminal pore. Six of the taste hairs have no tubular body containing dendrite at the base, and three unbranched dendrites running up to a terminal pore.     

Morphology and ultrastructure of the sensory spine,a presumed mechanoreceptor of Sphaeroma hookeri (Crustacea,Isopoda), and remarks on similar spines in other peracarids

The isopod Sphaeroma hookeri and many other isopods and peracarids have a sensory spine with laterally inserting sensory hair, positioned in the apical region of the propodal palm of pereopod 1. This spine is innervated by five to eight sensory cells (each giving rise to one cilium) the dendrites of which can be divided into an inner and outer dendritic segment. The cilia are surrounded by an extracellular, electron-dense dendritic sheath. Thirteen enveloping cells are present. The outer dendritic segment (structure beyond the basal bodies) contains two receptor lymph cavities; the inner one lying within the dendritic sheath is homologous with the inner receptor lymph cavity of insects. Scolopales, or tubular bodies, are lacking; their function is probably accomplished by the dendritic sheath. Apically the sensory hair does not have a pore, and the spine is heavily sclerotized. The inner dendritic segment begins with a basal body from which rootlets of different length and thickness extend into the dendrite. In the latter is an accumulation of vesicles. The dendrites keep close contact with other dendrites and the enveloping cells by desmosomal membrane structures. The possible importance of the sensory spine for phylogenetic studies is discussed.     

Sensory innervation monitoring movement and position in the mandibular stylets of the aphid, Brevicoryne brassicae

The sensory innervation of the mandibular stylets of the aphid Brevicoryne brassicae (L.) has been examined by electron microscopy. Two groups of sensory neurones are present in the mandible. Each has two neurones, one with a short dendrite extending into the base of the mandible and ending in the base and another with a long microtubular process which extends 500 m? down to the distal tip of the mandible. The two neurones are enclosed by an ensheathing cell comparable to the trichogen cell enveloping the group of neurones innervating pegs and hairs. This ensheathing cell is supported by extensive electron-dense filaments to form a scolopale and is embedded in the mass of stylet-forming cells at the base of the mandible. The inner segments of the dendrites are anchored to the ensheathing cell by desmosome junctions. Desmosome junctions also bind the microtubular outer segments of the short and long dendrite to each other. There is no evidence of a dendritic sheath enclosing the distal portion of the short dendrite which ends while still in the extracellular space within the ensheathing cell. The microtubular process of the long dendrite extends down the lumen of the mandible enclosed by a close-fitting extracellular sheath which penetrates and is attached to the cuticular wall of the mandible tip. Distally this sheath is thickened on one side. Deflection of the mandible would therefore deform the dendritic membrane asymmetrically because the thin walls of the sheath would bend more than the thick walls. This would exert an unequal mechanical strain on the dendritic membrane which could result in depolarization in response to deflection in a particular direction. The arrangement of the dendrites and their sheaths within the mandible is such that deflection to the right would distort one dendrite in the same way as deflection to the left would distort the other.     

Labellar taste organs of Drosophila melanogaster

There are 36 to 42 taste bristles on each half of the labellum of Drosophila melanogaster; most of them are two-pronged with a pouch between them. Some end bluntly with a pore at the tip. Each taste-bristle has two lumina: one is circular, the other crescent-like in cross section. In most bristles four dendrites of chemoreceptor neurons run along the circular lumen. In five to seven taste-bristles only two chemoreceptor neurons are found. A mechanoreceptor neuron sends a dendrite to the base of each taste-bristle. The dendrites are surrounded by four concentrically-arranged sheath cells. The inner cell secretes the cuticular sheath; cells II and III are presumably two trichogens, one secreting the bristle material around the circular lumen, the other around the crescent-like lumen. Cell IV, especially rich in bundles of microtubules, secretes the cuticle of the socket, and corresponds to the tormogen. The neurons have the typical structure found in insect sensilla. In many sensilla one neuron is less electron-dense than the others and may be the water-sensor. On the medial side of the labellum between the pseudotracheae are rows of taste pegs covered by folds. In each peg one chemoreceptor and one mechanoreceptor are found. The number of axons in each labial nerve agrees with the total number of dendrites in all taste organs of each lobe.     

The cercal sensilla of the blowfly Lucilia cuprina. I. Structure of the sockets and distal dendritic regions

The functions of the gustatory, olfactory, touch and stress receptors on the cerci of Lucilia cuprina Wied. (Diptera: Calliphoridae) are apparent from the morphology of their distal dendritic segments and associated cuticular structures. Each trichoid mechanoreceptor has a dendrite containing a tubular body at the base of the hairshaft. The suspension fibres and socket septum may be involved in transmitting a stimulus to the dendrite terminal and restoring the hair to its resting position. The campaniform sensilla are considered as trichoid mechanoreceptors with reduced hair shafts and socket structures, reflected in fusion of the suspension fibres into the inner cuticle of the dome and loss of the socket septum. Fusion and reduction of the socket structures is also apparent at the bases of the olfactory pegs. They differ from typical antennal olfactory sensilla in having a flexible socket and relatively thick walls; features which may protect them from damage during ovipositor probing of potential oviposition substrates. The two types of cereal gustatory sensilla differ in their complement of chemosensory dendrites, one has three, the other four, the latter type also has a mechanoreceptive dendrite at the base of the hair shaft. Both types have socket structures resembling those of the trichoid mechanoreceptors.     

Light microscopic studies on the pineal organ in teleost fishes with special regard to its function

The antennal flagellum of the male sorghum midge is about a millimeter long and may bear over 500 sense organs. These consist of (1) tactile hairs, (2) thin-walled pegs, (3) circumfila and (4) very small pegs of unknown function. Each of the 12 subsegments of the flagellum is divided into two globular nodes and each of these is encircled by a circumfilum of from 6 to 14 loops. The circumfila are attached to the antennal surface by short stalks. The loops of the circumfila have the basic structure of thin-walled chemoreceptors: (1) very small pores in their delicate wall and (2) a lumen filled with branches of dendrites from sensory neurons. The outer surface of the circumfilum is covered with a labyrinth of fine ridges between which the pores are located. Some evidence was obtained that the circumfila are produced in the pupa by bifurcate trichogen cells. The flagellum of the female is shorter than that of the male and composed of 12 cylindrical subsegments. The circumfila of the female lie close to the surface to which they are attached by short stalks. Each is composed of two parts that encircle the subsegment and of two others that run lengthwise between the circles. The surface is nearly smooth, perforated by fine openings and lacks the complex pattern of ridges seen in the male. It also has more dendrite branches but, otherwise, has the same basic structure.     

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

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

The fine structure of a cephalic sensory receptor in the copepod Doropygus seclusus Illg (Crustacea: Copepoda: Notodelphyidae)

A cephalic organ of presumed sensory function is described in nauplii and copepodids of the ascidicolous copepod Doropygus seclusus Illg. The receptor, located bilaterally in the anterodorsal head region, is composed of dendrites of extra optic protocerebral origin which have ciliary protrusions with basal bodies, no rootlets, and a basal infrastructure of the 9 + 0 type. The cilia do not branch and their distal terminations contain only one to four microtubules. In nauplii and free-living copepodids, a large epidermal supporting cell encapsulates the end of one dendrite and its cilia in a sac. Other dendrites and their cilia pass through the supporting cell and, terminally, the cilia escape to form a whorled fascicle which contacts the anterolateral cephalic cuticle. The latter end organ reaches its greatest development in the second copepodid stage — the stage which infects the ascidian. All of the symbiotic stages of the copepod have only a proportionately smaller end organ of the saccular type and apparently lack the end organ consisting of whorls of ciliary ends. The function of the receptor is unknown, but it is suggested that the end organ which disappears in the symbiotic stages functions in second copepodids in host recognition.     

The Ultrastructure of a Chemoreceptor Organ in the Head of Copepod Crustaceans

The ultrastructure of the paired nerves, previously called frontal organ or X-organ, in copepod crustaceans was investigated. These nerves, running from the anterior margin of the brain to the frontal edge of the animals, are found to contain the dendrites of three types of morphologically different sensory neurons. The first unit consists of two dendrites (distinguished by their myelinization) leading to two small hairs on the front. Their detailed structure was not investigated. The second unit consists of a few large dendrites ending in branching cilia. The latter are surrounded by a specialized glial cell. The ciliary branches are regularly sized and arranged. The third unit consists of c. 17 dendrites ending with cilia at the cuticle. The cilia are split into irregular branches which are buried in modified epidermal cells which, in the case of Calanus, are connected with cuticular pores. By analogy with other presumed chemosensory organs in the Arthropoda, the second and the third unit are considered, on a morphological basis, to be chemoreceptors. The second unit receives internal stimuli. Because it resembles other X-organs in the Crustacea, all X-organs could have the same function. The third unit is thought of as receiving external stimuli.     

Ultrastructure of antennal sensilla of the peach aphid Myzus persicae Sulzer, 1776

The antennal sensilla of alate Myzus persicae were mapped using transmission electron microscopy and the ultrastructure of sensilla trichoidea, coeloconica, and placoidea are described. Trichoid sensilla, located on the tip of the antennae, are innervated by 2–4 neurons, with some outer dendrites reaching the distal end of the hair. Coeloconic sensilla in primary rhinaria are of two morphological types, both equipped with two dendrites. Dendrites of Type II coeloconic sensilla are enveloped in the dendrite sheath, containing the sensillum lymph. In sensilla coeloconica of Type I, instead, dendrites are enclosed by an electron opaque solid cuticle, with no space left for the sensillum lymph. The ultrastructure of big placoid sensillum reveals the presence of three groups of neurons, with 2–3 dendrites in each neuron group, while both small placoid sensilla are equipped with a single group of neurons, consisting of three dendrites. Both large and small placoid sensilla bear multiple pores on the outer cuticle. The function of these sensilla is also discussed. J. Morphol. 276:219–227, 2015. © 2014 Wiley Periodicals, Inc.     

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.     

Sensory cell degeneration in the ontogeny of the chemosensitive sensilla in the labial palp-pit organ of the butterfly,Pieris rapae L. (Insecta,Lepidoptera)

Summary The ontogeny of the chemoreceptive sensilla in the labial palp-pit organ was studied in Pieris rapae by examining twelve successive stages between pupation and emergence of the imago, which takes a period of 160 h under the experimental conditions. Mitoses occur until 20 h after pupation. They lead to anlagen of sensilla, 91% of which are comprised of three sensory cells. However, two sensory cells degenerate in each sensillum during a period of 28 h. The same process occurs in anlagen with four sensory cells resulting in bicellular sensilla. Axons grow out only after the number of sensory cells has been reduced. Further consecutive steps in sensory cell differentiation are: (a) outgrowth of dendritic outer segment and dendrite sheath; (b) outgrowth of trichogen process and change in structure of elongating dendrite sheath; (c) deposition of cuticle and pore tubules in the pegs; (d) retraction of trichogen process; (e) increase in diameter of dendritic outer segment accompanied by increase of microtubule number and appearance of regularly spaced electron-dense bodies at tubular doublets; (f) branching of dendritic outer segment; and (g) transformation of the dendritic branches into curled lamellae and partial destruction of the dendrite sheath. The unique process of sensory cell degeneration is interpreted as an event that revokes a step towards a possible functional improvement of the labial palp-pit organ during further evolutionSupported by the Deutsche Forschungsgemeinschaft (SFB 4/G1)     

Fine structure of the tip of the labellar taste hair of the blow flies,Phormia regina (Mg.) and Calliphora vicina R.-D. (Diptera,Calliphoridae)

Summary The labellar taste hairs of the blow flies, Phormia regina and Calliphora vicina, have an opening mechanism at the tip which consists of two stump cuticular prongs and a funnel-like cuticular pouch. Opening and folding of these structures are regulated by the pressure within the dendrite-free lumen of the hair. The extrusion of viscous substance at the tip of the taste hair is possible through spongy cuticle and one pore in each prong; it seems likewise to depend on the pressure within the dendrite-free lumen and results in regional collapsing of this lumen. Described and discussed are: The cuticle and pores of the structures at the hair tip, pore filaments which extend from the dendrites, and the number and arrangement of the dendrites.This work was supported by a grant from the 7USDA, Entomology Research Division, Beltsville, Md., and the grant GB-13500 from the National Science Foundation.We thank Dr. J. F. Worley, USDA, Plant Science Research Division, Beltsville, Md., for his collaboration in fluorescence microscopy.     

Morphology and ultrastructure of sense organs on the ovipositor of Trybliographa rapae,a parasitoid of the cabbage root fly

The ovipositor of the parasitoid wasp Trybliographa rapae was examined by scanning and transmission electron microscopy. Characteristic peg-like sensilla with a cuticular ring at the base are found at the tip of the ventral valves, where they occur in a characteristic arrangement of triplets. The unusual basal structure probably protects the sensilla against damage during movement through the substrate and piercing of the host cuticle. These sensilla are each innervated by six dendrites, some of which have lamellated tips, generally considered to be characteristic of thermosensitivity. It is suggested that the remaining dendrites are gustatory, and as such probably respond to factors present in host haemolymph. A second type of peg-like sensillum is found on both the dorsal and the ventral valves. These are set in deep pits so that only the tip of the peg protrudes above the surface of the cuticle. These occur along the length of the ovipositor shaft and ultrastructural studies reveal the pegs to be innervated by a single mechanosensitive dendrite, probably monitoring the movement of the ovipositor through the substrate.     

Chiton integument: Ultrastructure of the sensory hairs of Mopalia muscosa (Mollusca: Polyplacophora)

Summary The dorsal integument of the girdle of the chiton Mopalia muscosa is covered by a chitinous cuticle about 0.1 mm in thickness. Within the cuticle are fusiform spicules composed of a central mass of pigment granules surrounded by a layer of calcium carbonate crystals. Tapered, curved chitinous hairs with a groove on the mesial surface pass through the cuticle and protrude above the surface. The spicules are produced by specialized groups of epidermal cells called spiniferous papillae and the hairs are produced by trichogenous papillae. Processes of pigment cells containing green granules are scattered among the cells of each type of papilla and among the common epidermal cells.The wall or cortex of each hair is composed of two layers. The cortex surrounds a central medulla that contains matrix material of low density and from 1 to 20 axial bundles of dendrites. The number of bundles within the medulla varies with the size of the hair. Each bundle contains from 1 to 25 dendrites ensheathed by processes of supporting cells. The dendrites and supporting sheath arise from epidermal cells of the central part of the papilla. At the base of each trichogenous papilla are several nerves that pass into the dermis. Two questions remain unresolved. The function of the hairs is unknown, and we have not determined whether the sensory cells are primary sensory neurons or secondary sensory cells.