The Fine Structure of a Sensory Organ of a Cladocop Ostracode (Crustacea) Belonging to the Organ of Bellonci (Sensory Pore) Complex

Andersson, A. 1980. The fine structure of a sensory organ of a cladocop ostracode (Crustacea) belonging to the organ of Bellonci (sensory pore) complex. (Department of Zoology, University of Lund, Sweden.) — Acta zool. (Stockh.) 61(1): 51–58. The organ of Bellonci, a complex of cephalic receptors, has previously been reported from two ostracode groups. On morphologic grounds, a cephalic receptor of a third ostracode group (Cladocopa) is believed to be an organ of Bellonci. The organ is situated on the forehead above the first pair of antennae and consists of two feathered hairs. Two nerves, each formed by one dendrite, run from the protocerebrum into the hairs where they terminate with ramose cilia. The dendrites, as well as the cilia and ciliary branches, are enveloped by glial cells. Distally, these cells form cavities around the ciliary branches. The ciliated neuronal connection and the glial cavities, together with other morphologic characteristics of the organ, support a homologization with the organ of Bellonci of other myodocopid ostracodes.     

The structure of the organ of bellonci of the syncarid crustacean,Anaspides tasmaniae (Thomson)

Summary The organ of Bellonci of Anaspides tasmaniae (Thomson) (Crustacea, Syncarida) is described light and electron microscopically, and a few histochemical tests are reported. Located ventrally in the eyestalk below the medulla interna, the organ is composed of a number of cavities. These are similar in structure in their contents and associated cellular components, which include two types of glia cells delimiting each cavity and the terminal parts of a few dendrites. Each dendrite usually bears two cilia, which project into the cavity where they split up into numerous branches. The organ is supplied by three nerve tracts: two from the medulla terminalis and one from the medulla interna. The sensory pore, which is innervated from the medulla interna, is not closely associated with the organ of Bellonci in Anaspides. No marked secretory activity is detectable by histochemical or ultrastructural observations. It is thought that the organ has a sensory function.This investigation was supported by a grant (to T.K.) from Helge Ax:son Johnsons Stiftelse. One of us (P.S.L.) was on sabbatical leave from the University of Tasmania.     

Ultrastructure of the nuchal organ and cerebral organ in Onchnesoma squamatum (Sipuncula, Phascolionidae)

 The ultrastructure of the nuchal organ and cerebral organ is described for the first time in a species of the Sipuncula, Onchnesoma squamatum. The nuchal organ is an unpaired structure lying outside and dorsal to the tentacular crown; furrows give the organ a paired appearance. The cerebral organ is an unciliated pad anterior to the nuchal organ. The nuchal organ consists of ciliated supporting cells, non-ciliated supporting cells and bipolar primary sensory cells. The cerebral organ is composed of unciliated supporting cells and numerous bipolar sensory cells. This clearly favours the hypothesis that this structure has a sensory function in adults rather than being a vestige of a larval organ. The sensory cells are similar in both organs and exhibit features indicative of chemoreception. Since the density of the sensory cells is low in the nuchal organ, an exclusively sensory function is questioned. There is some evidence that the two organs represent a functional unit. The present findings do not support the view that the nuchal organs of Sipuncula and ”Polychaeta” are homologous, but instead suggest that they are convergent structures. Accepted: 18 September 1996     

Structure of the green lacewing tympanal organ (Chrysopa carnea,neuroptera)

Small swellings near the base of the radial vein in each fore wing of the green lacewing, Chrysopa carnea, resemble typical insect tympanal organs, but some important differences are apparent. The swellings are bounded dorsally and laterally by thick cuticle and ventrally by thin, membranous cuticle. The ventral membrane is formed by a single, thin sheet of exocuticle with flattened hypodermis internally, but lacks the tracheal component that forms part of the tympanum in the typical insect tympanal organ. The portion of the membrane beneath each swelling is rippled while proximally it is smooth. In contrast to typical insect tympanal organs, the swellings in C. carnea are largely fluid-filled since an unexpanded trachea runs through each organ. A distal and a proximal chordotonal organ composed of typical chordotonal sensory units are associated with each swelling. The distal organ contains from five to seven units while the proximal organ is composed of from 18 to 20 units. Each sensory unit is composed of three readily identifiable cells. Distally, an attachment cell unites with the membrane and is contiguous with the scolopale cell, which surrounds the dendrite of the bipolar neuron. On the basis of the morphological evidence, one would not expect these swellings to function as sound receptors. However, the results of physiological and behavioral experiments, presented elsewhere, show that these organs are receptors for ultrasound.     

Histology and ultrastructure of the olfactory organ of the freshwater pulmonate Helisoma trivolvis

Summary The olfactory organ of Helisoma trivolvis is located on the surface of the body at the base of the cephalic tentacles. An evagination of skin, the olfactory plica, at the base of the tentacle extends over the olfactory organ dorsally. The epithelium of the olfactory organs contains unspecialized epithelial cells, ciliated epithelial cells, basal cells, mucous secretory cells, and sensory dendrites. The surface of the epithelium has a complex brush border of thick plasmatic processes, which branch to form several terminal microvillar twigs. Long slender cytoplasmic processes form a dense spongy layer among the plasmatic processes beneath the level of the terminal twigs. Bipolar primary sensory neurons clustered beneath the epithelium of the olfactory organ send dendrites through the epithelium to the free surface. Some sensory endings have a few short cilia, but most bear only microvilli. Cilia of sensory endings and epithelial cells extend beyond the brush border of the epithelium. Small axons arise from the perikarya of the sensory neurons and enter a branch of the olfactory nerve. HRP tracing indicates that the axons pass to the cerebral ganglion without interruption. Histochemical tests indicate that the sensory neurons are neither aminergic nor cholinergic.     

The Organ of Bellonci in Ostracodes: An Ultrastructural Study of the Rod-shaped,or Frontal,Organ

Ultrastructural observations of the rod-shaped organ in Cypridina norvegica and Paraconchoecia elegans indicate homology with the organ of Bellonci of other crustaceans. In C. norvegica the organ is situated close to the ventral cup of the nauplius eye. Distally in the organ, several ciliary ramifications of the sensory neurons protrude into internal cavities formed by bordering cells. Six dendrites, with cell bodies within and in front of the brain, form the proximally bifurcated nerve, which enters the protocerebrum in the region of the medullae terminales. In this species the organ represents the deep receptor of the organ of Bellonci complex. In P. elegans the external part of the organ is situated between the proximal parts of the antennulae. Four dendrites in two groups emerge from the protocerebrum. Distally, they form branching cilia that are in close contact which the cuticle of the organ, thus forming a receptor similar to the superficial receptor of the organ of Bellonci complex of other crustaceans. It is suggested that the terms frontal organ and rod-shaped organ be abandoned in favour of the term organ of Bellonci.     

Ultrastructure of the nuchal organs in the polychaete Platynereis dumerilii (Annelida,Nereididae)

Abstract. We examined the nuchal organs of adults of the nereidid polychaete Platynereis dumerilii by means of scanning and transmission electron microscopy. The most prominent features of the nuchal organs are paired ciliary bands located dorsolaterally at the posterior margin of the prostomium. They are composed of primary sensory cells and multiciliated supporting cells, both covered by a thin cuticle. The supporting cells have motile cilia that penetrate the cuticle and are responsible for the movement of water. Subapically, they have a narrowed neck region; the spaces between the neck regions of these supporting cells comprise the olfactory chamber. The dendrites of the sensory cells give rise to a single modified cilium that crosses the olfactory chamber; numerous thin microvillus-like processes, presumably extending from the sensory cells, also traverse the olfactory chamber. At the periphery of the ciliated epithelium runs a large nervous process between the ciliated supporting cells. It consists of smaller bundles of sensory dendrites that unite to form the nuchal nerve, which leaves the ciliated epithelium basally and runs toward the posterior part of the brain, where the perikarya of the sensory cells are located in clusters. The ciliated epithelium of the nuchal organs is surrounded by non-ciliated, peripheral epidermal cells. Those immediately adjacent to the ciliated supporting cells have a granular cuticle; those further away have a smooth cuticle. The nuchal organs of epitokous individuals of P. dumerilii are similar to those described previously in other species of polychaetes and are a useful model for understanding the development of nuchal organs in polychaetes.     

Ultrastructure of the nuchal organ in the interstitial polychaete Stygocapitella subterranea (Parergodrilidae)

The nuchal organs of Stygocapitella subterranea are paired narrow pits. They are lined by unciliated cells at the opening and by ciliated cells at the basal parts. The primary sensory cells (6–8) are arranged in a single patch at the bottom of the nuchal pit. The nuclei of the sensory cells are located in the posterior portion of the brain. Their dendrites form the nuchal nerve which is sheathed by the ciliated cells. Each sensory cell bears up to 4 modified sensory cilia and several microvilli extending into the olfactory chamber. The sensory cilia show various patterns of axonemal organization and have no rootlets. The olfactory chamber is covered by a cuticular matrix. Another primary sensory cell lies at the opening of the nuchal pit. It bears cilia which penetrate the cuticle but are enveloped by the epicuticle. Retractor muscles insert caudally on the organ. The nuchal organ of S. subterranea shows similarities to those of opheliids but exhibits several features not to be found in other nuchal organs.     

The coxo-trochanteral muscle receptor organ of locusts

Summary The coxo-trochanteral muscle receptor organ of the hind leg of the locust Locusta migratoria migratorioides (R.&F.) has been investigated by use of scanning and transmission electron microscopy with special emphasis on its distal attachment site. The overall morphology of the receptor muscle, the sensory neuron and its dendrites was found to share many common features with other arthropod sense organs of that type with two important differences: (1) the connective tissue segment (= intercalated tendon) is extremely short compared to that of other muscle receptor organs; (2) the naked dendritic terminals of the non-ciliated, multipolar sensory neuron of the organ contain clusters of microtubules, interconnected by an amorphous matrix, that resemble the tubular bodies of ciliated, epithelial receptor cells.Abbreviation MRO muscle receptor organ Supported by the Deutsche Forschungsgemeinschaft (Br 882 and Hu 223)     

TEM studies on the lattice organs of cirripede cypris larvae (Crustacea, Thecostraca, Cirripedia)

 Lattice organs consist of five pairs of sensory organs situated on the dorsal carapace in cypris larvae of the Crustacea Cirripedia. The lattice organs in cypris larvae of Trypetesa lampas (Acrothoracica) and Peltogaster paguri (Rhizocephala) represent the two main types found in cirripedes, but only minor differences exist at the TEM level. Each lattice organ is innervated by two bipolar, primary receptor cells. The inner dendritic segment of each receptor cell carries two outer dendritic segments. The outer dendritic segments contain modified cilia with a short ciliary segment (9×2+0 structure). Two sheath cells envelop the dendrite except for the distal ends of the outer dendritic segments. This distal end enters a cavity in the carapace cuticle and reaches a terminal pore situated at the far end of the cavity. The cuticle above the cavity is modified. In both species the epicuticle is partly perforated by numerous small pores and the underlying exocuticle is much thinner and less electron dense than the regular exocuticle. Lattice organs very probably have a chemosensory function and are homologous with the sensory dorsal organ of other crustacean taxa. Accepted: 18 August 1998     

Olfactory metamorphosis in the coastal tailed frog Ascaphus truei (Amphibia,Anura, Leiopelmatidae)

The structure of the olfactory organ in larvae and adults of the basal anuran Ascaphus truei was examined using light micrography, electron micrography, and resin casts of the nasal cavity. The larval olfactory organ consists of nonsensory anterior and posterior nasal tubes connected to a large, main olfactory cavity containing olfactory epithelium; the vomeronasal organ is a ventrolateral diverticulum of this cavity. A small patch of olfactory epithelium (the “epithelial band”) also is present in the preoral buccal cavity, anterolateral to the choana. The main olfactory epithelium and epithelial band have both microvillar and ciliated receptor cells, and both microvillar and ciliated supporting cells. The epithelial band also contains secretory ciliated supporting cells. The vomeronasal epithelium contains only microvillar receptor cells. After metamorphosis, the adult olfactory organ is divided into the three typical anuran olfactory chambers: the principal, middle, and inferior cavities. The anterior part of the principal cavity contains a “larval type” epithelium that has both microvillar and ciliated receptor cells and both microvillar and ciliated supporting cells, whereas the posterior part is lined with an “adult‐type” epithelium that has only ciliated receptor cells and microvillar supporting cells. The middle cavity is nonsensory. The vomeronasal epithelium of the inferior cavity resembles that of larvae but is distinguished by a novel type of microvillar cell. The presence of two distinct types of olfactory epithelium in the principal cavity of adult A. truei is unique among previously described anuran olfactory organs. A comparative review suggests that the anterior olfactory epithelium is homologous with the “recessus olfactorius” of other anurans and with the accessory nasal cavity of pipids and functions to detect water‐borne odorants. J. Morphol. 2011. © 2011 Wiley Periodicals, Inc.     

Ultrastructural investigation of the nuchal organs ofPygospio elegans (Polychaeta). I. Larval nuchal organs

The structural differentiation of the nuchal organs during the post-embryonic development ofPygospio elegans is described. The sensory organs are composed of two cell types: ciliated cells and bipolar primary sensory cells, constituting the nuchal ganglion, which is associated with both the sensory epithelium and the brain. Since the sensory neurons are largely integrated into posterolateral parts of the cerebral ganglion, the nuchal organs are primary presegmental structures. The microvilli of the ciliated cells form a cover over the cuticle with a presumed protective function. An extracellular space extends between cuticle and sensory epithelium. The distal dendrites of the sensory cells terminate in sensory bulbs, bearing one modified sensory cilium each that projects into the olfactory chamber, embedded within the secretion of the ciliated cells. During development, the nuchal organs increase in size. This is accompanied by a shift in position, an expansion of the sensory area, and secretory activity of the ciliated cells. The nuchal ganglion differentiates into three nuchal centres forming three distinct sensory areas around the ciliated region. Each nuchal complex reveals two short nuchal nerves comprising the sensory axons, which enter the posterior circumesophageal connective. The sensory cells lying in the brain exhibit neurosecretory activity; the sensory cilia enlarge their surface area by dilating and branching. Nuchal organs accomplish the basic structural adaptions of chemoreceptors and show structural analogies to arthropod olfactory sensilla; thus, there is every reason to suppose chemoreceptor function.     

Structure of the temporal organ of the Japanese house centipede,Thereuonema hilgendorfi Verhoeff

The ultrastructure of the temporal organ of the Japanese house centipede, Thereuonema hilgendorfi Verhoeff (Chilopoda), has been examined. The temporal organ of this species is known to be a carbon dioxide receptor. It appears externally as a small protuberance with a small opening (5 μm) on its summit. There is a small cuticle-lined cavity beneath the protuberance, and a mushroom-shaped projection protrudes from the base of the cavity into its interior. Below the cavity is an encapsulated, bulb-shaped cellular mass (sensory bulb), which contains about ten receptor cells and 100 supporting cells. Nuclei of both receptor and supporting cells occur basally in the sensory bulb. Each receptor cell has a single dendrite, which gives rise to a pair of sensory cilia. The cilia enter the mushroom-shaped projection, and course along the inner surface of its calyx. The supporting cells have distal processes, which accompany the cilia into the calyx. The surface cuticle of the calyx consists of a fabric of fibrils, but in not layered like the cuticular integument. The fabric is permeable to water. The observed structure is discussed in relation to carbon dioxide reception and in comparison with the structure of olfactory receptors and hygroreceptors.     

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 presumptive light sensitive ciliary organs in larvae of Poecilochaetidae,Trochochaetidae, Spionidae,Magelonidae (Annelida) and its phylogenetic significance

Larvae of Poecilochaetus serpens, Trochochaeta multisetosum and Polydora ciliata possess almost identical unpigmented, ciliary, presumptive light sensitive organs within the prostomium. The data corroborate hypotheses on the close relationship of Poecilochaetidae, Trochochaetidae and Spionidae and are even congruent with inclusion of Poecilochaetidae and Trochochaetidae within Spionidae. The organs in P. serpens, T. multisetosum and P. ciliata are composed of one monociliary receptor cell, one supportive cell and several associated flask shaped bipolar sensory cells. The receptor cell cilium enters the supportive cell cavity through a thin pore, dilates and then branches into a high number of disordered projections. The associated sensory cells bear one or occasionally two cilia, which run horizontally beneath or within the cuticle. The supportive cell cavity is not sealed by any cell contact from the subcuticular extracellular space. The organs in Magelona mirabilis are composed of a single supportive cell, but several receptor cells. No further sensory cells are associated. Each receptor cell sends one cilium into an own invagination of the supportive cell, and the ciliary branches are highly ordered. The examined organs in P. serpens, T. multisetosum and P. ciliata exhibit a unique organization amongst polychaetes. The organs of M. mirabilis are most probably homologous. A homology to ciliary organs of Protodrilida is conceivable. In the lineage leading to Protodrilida, primary larval organs may have been integrated into the adult body organization by heterochrony.     

Morphology and ultrastructure of the organ of Bellonci in the marine amphipod Gammarus setosus

The three-dimensional structure of the organ of Bellonci in the marine amphipod Gammarus setosus and the relationship between its sensory cells and concretion are described using light, transmission, and scanning electron microscopy, with chemical treatment for cell lysis, calcium chelation, glycogen staining, and lanthanum labelling. The organ is encapsulated and has three units called fuselli. Each is enclosed by two fusellar cells which generate and release calcium granule strands into the cores of the fusellar concretions, which are united in the center of the organ. The surface of each fusellus is traversed by spiral dendrites entering dorsally and ending ventrally. The spiral dendrites arise from sensory neurons contained in a palm-shaped ganglion in the center of the capsule, beyond which they are twisted like a rope before reaching the concretion. The spiral dendrites are linked in pairs by gap and tight junctions and each gives origin to two pairs of 9+0 sensory cilia 30 μm apart. The ciliary distal segments give rise to long tubules which are in contact with the calcium granule strands. The ciliary proximal segments are expanded by many long mitochondria which interdigitate with the branched striated ciliary rootlets. The concretion is suspended in the capsule cavity by axons originating from four neurons of a remote mechanoreceptor. The structure of the organ suggests that it is a sensory organ involved in the reception and integration of a variety of stimuli.     

Ultrastructural investigations on the nuchal organ of the protandric polychaete,Ophryotrocha puerilis (Polychaeta,Dorvilleidae)

Summary The nuchal organs of the protandric hermaphrodite Ophryotrocha puerilis were studied by electron microscopy. Ophryotrocha puerilis is the first species hitherto described which possesses four instead of two nuchal organs. These sensory structures are located as ciliary pits at the posterior margin of the prostomium. Histologically, the nuchal organs are composed of supporting cells with long motile cilia and bipolar sensory cells, the perikarya of which form four distinct nuchal ganglia adjoining the brain. These structural components are concentrically arranged around the central sensory area. This area is covered by a modified cuticle, whereas the cuticle above the peripheral region of the sense organ exhibits the appearance typical for polychaetes. Two types of vesicular material are produced in the basal supporting cells, a dense-cored one within the central supporting cells only and a clear irregular-shaped one in all of these cells. The first type is considered to be responsible for the formation of the modified cuticle. The significance of these most probably long-distance chemoreceptory organs and their possible role in reproductive behaviour is discussed.     

The accessory organ,a scolopidial sensory organ,in the cave cricket Troglophilus neglectus (Orthoptera: Ensifera: Rhaphidophoridae)

Mechanoreceptor organs occur in great diversity in insect legs. This study investigates sensory organs in the leg of atympanate cave crickets (Troglophilus neglectus KRAUSS, 1879) by neuronal tracing. Previously, the subgenual and the intermediate organs were recognised in the subgenual organ complex, lacking the tympanal membranes present for example in the tibial hearing organs of Gryllidae and Tettigoniidae. We document the presence of the accessory organ in T. neglectus. This scolopidial organ is located in the posterior tibia close to the subgenual organ and can be identified by position, innervation and orientation of the dendrites of sensory neurons. The main motor nerve in the leg innervates a part of the subgenual organ and the accessory organ. The dendrites of sensory neurons in the accessory organ are characteristically bent in proximo‐dorsal direction, while the subgenual organ dendrites run distally along the longitudinal axis of the leg. The accessory organ contains 6–10 scolopidial sensilla, and no differences in neuroanatomy occur between the three thoracic leg pairs. Hence, the subgenual organ complex in cave crickets is more complex than previously known. The wider taxonomic distribution of the accessory scolopidial organ among orthopteroid insects is inconsistent, indicating its repeated losses or convergent evolution.     

Morphology and histochemistry of the peripheral olfactory organ in the round goby,Neogobius melanostomus (Teleostei: Gobiidae)

This first comprehensive study of the peripheral olfactory organ from a representative of the large and economically important order of teleost fishes, the Perciformes, shows a compact structure with olfactory sensory neurons distributed widely throughout the olfactory chamber. The spatial organization of the nasal cavity in the bottom-dwelling round goby (Gobiidae, Neogobius melanostomus) was examined using impression material injection, immunocytochemistry, and transmission electron microscopy. The olfactory chamber contains a single olfactory lamella; prominent dorsocaudal lachrymal and ethmoidal accessory nasal sacs are situated ventrocaudal to the chamber. The location of the olfactory mucosa within the olfactory chamber is novel for teleost fish, as it extends beyond the ventral surface to the lateral and dorsal regions. Microvillar olfactory sensory neurons and ciliated olfactory sensory neurons were identified by transmission electron microscopy and the spatial distribution of these two cell types was assessed through immunocytochemistry against olfactory receptor coupled G-proteins. Both G(alphaolf)-immunoreactive ciliated olfactory sensory neurons and the G(alphao)-immunoreactive microvillar form were located throughout the olfactory epithelium. Ciliated crypt cells were G(alphao) immunoreactive and were found throughout the olfactory epithelium of some specimens. The widespread occurrence of olfactory sensory neurons in the olfactory chamber supports the idea that olfactory signaling is important to the survival of the round goby. The prominence of the lachrymal and ethmoidal accessory nasal sacs indicates the capacity to regulate the flow of odorant molecules over the sensory surface of the olfactory sensory neurons, possibly through a pump-like mechanism driven by opercular activity associated with gill ventilation.