The attachment complex of brachiolaria larvae of the sea star <Emphasis Type="Italic">Asterias rubens</Emphasis> (Echinodermata): an ultrastructural and immunocytochemical study

The attachment complex of brachiolaria larvae of the asteroid Asterias rubens comprises three brachiolar arms and an adhesive disc located on the preoral lobe. The former are used in temporary attachment and sensory testing of the substratum, whereas the latter is used for permanent fixation to the substratum at the onset of metamorphosis. Brachiolar arms are hollow structures consisting of an extensible stem tipped by a crown of dome-like ciliated papillae. The papilla epidermis is composed of secretory cells (type A, B and C cells), non-secretory ciliated cells, neurosecretory-like cells and support cells. Type A and B secretory cells fill a large part of the papilla epidermis and are always closely associated. They presumably form a duo-gland adhesive system in which type A and B cells are respectively adhesive and de-adhesive in function. The adhesive disc is an epidermal structure mainly composed of secretory cells and support cells. Secretory cells produce the cement, which anchor the metamorphic larva to the substratum until the podia are developed. The relatedness between the composition of the adhesive material in the brachiolaria attachment complex and in the podia of adults was investigated by immunocytochemistry using antibodies raised against podial adhesive secretions of A. rubens. Type A secretory cells were the only immunolabelled cells indicating that their temporary adhesive shares common epitopes with the one of podia. The attachment pattern displayed by the individuals of A. rubens during the perimetamorphic period—temporary, permanent, temporary—is unique among marine non-vertebrate Metazoa.     

The structure of the larval nervous system of Pisaster ochraceus (Echinodermata: Asteroidea)

Ultrastructural observations and glyoxilic acid-induced fluorescence of catecholamines indicate that tracts of axons lie at the base of the ciliary bands and run throughout their length in bipinnaria and brachiolaria larvae of Pisaster ochraceus. Two types of nerve cells occur at regular intervals within the ciliary bands. Type I nerve cells are associated with the axonal tracts, and type II nerve cells, which are ciliated, occur along the edge of the ciliary bands. Two prominent ganglia, which appear as accumulations of nerve cells and neuropile, occur on the lower lip of the larval mouth. Smaller ganglia occur irregularly throughout the ciliary band. Synapses were never clearly identified and were assumed to be unspecialized. Nervous tissues were also found associated with the esophageal muscles, the attachment organ, and the larval arms. Organization of the nervous system and its association with effectors suggest it controls swimming and feeding. Several similarities exist between the nervous systems of larval asteroids, larval echinoids, and adult echinoderms.     

Structural and ultrastructural analysis of the gills in the bacterial-bearing species <Emphasis Type="Italic">Thyasira falklandica</Emphasis> (Bivalvia,Mollusca)

In this study, the cellular organization of the gill that harbors symbiotic bacteria is described in the thyasirid Thyasira falklandica collected from South Shetlands in Antarctic. Sections of the gills revealed that T. falklandica belongs to the gill type 3, as described by Dufour (Biol Bull, 208:200–212, 2005), with an elongated lateral zone along the frontal-abfrontal axis of the gill filaments. The ciliated and intermediary zones looked similar to those described in symbionts-bearing bivalves. The lateral zone is more complex in T. falklandica than in other Thyasiridae already described. Such a zone is composed of four different cell types. Bacteriocytes are abundant in the frontal and abfrontal positions, while the middle part of the lateral zone is occupied mostly by numerous granule cells devoid of bacteria. All along the lateral zone, TEM and SEM observations show some ciliated cells, which are regularly interspersed between bacteriocytes and/or granule cells. Such cells, according to the long double ciliary roots of their cilia, should have a sensory function. Intercalary cells, which have never been observed between bacteriocytes, are restricted to the middle part of the lateral zone where their expansions overlap the adjacent granule cells. Bacterial symbionts occur only extracellularly among long microvilli differentiated by the bacteriocytes. They are abundant, usually spherical in shape (around 0.7 μm length), and covered by the glycocalix from bacteriocyte microvilli. According to TEM views, the empty vesicles located in the periplasmic space should be sulfur storage, as known for other sulfur-oxidizing symbionts.     

Morphology of the intestine of prefeeding and feeding adult Lampreys,Petromyzon marinus L.: The mucosa of the diverticulum,anterior intestine,and transition zone

Light and electron microscopy were used to examine the morphology of the mucosa of the diverticulum, anterior intestine, and transition zone in prefeeding and spontaneously feeding adult lampreys (Petromyzon marinus L.). Absorptive (either types A or B), ciliated, and enteroendocrine cells are present in all regions but the diverticulum and anterior intestine also possess zymogen (secretory) cells. Type A absorptive cells are restricted to the diverticulum and the rostral one-third of the anterior intestine and are characterized by abundant mitochondria and an extensive smooth tubular network. Type B absorptive cells, in the remainder of the anterior intestine and the transition zone, possess small numbers of these organelles but in the transition zone also have inclusion bodies. During feeding, abundant lipid droplets and lipoprotein (VLDL) accumulate in the cytoplasm of both types of absorptive cells and in the lateral intercellular and the perivascular spaces. Lipid is present to a limited extent in ciliated cells and is encountered only rarely in enteroendocrine and zymogen cells. Although the animals are obligate sanguivores, there is little evidence of iron within these mucosal cells. It is suggested that intestinal efficiency displayed by this animal is due in part to ion transport in osmoregulation in type A cells, lipid absorption in types A and B cells, and digestion through enzymes in zymogen cells.     

Ultrastructural studies on the ciliated receptors of the long tentacles of the giant scallop,Placopecten magellanicus (Gmelin)

Summary The long tentacles of the Giant scallop Placopecten magellanicus (Gmelin) have been examined with light, scanning, and transmission electron microscopy. Three types of ciliated cells have been observed, one of which is located in specialised papillae born on the distal third of the tentacle. There are two separate cell types within the papillae. Type I cells are non-ciliated supporting cells, which form a capsule within which are found the Type II cells. These cells bear up to five cilia at their apices, and it is suggested that these are the receptor cells of the organ. No function has yet been determined for the receptors, but is suggested that they might be mechanoreceptors. A third cell type, Type III cells, occur at the base of the papillae. These cells bear many cilia and also macrocilia. Another ciliated cell type occurs on the proximal two thirds of the tentacle. These cells bear many cilia that are thought to be motile and not sensory.This research was supported by National Research Council of Canada Operating Grant No. A-6444 to Dr. V.C. Barber. Additional support came from the Department of Biology and School of Graduate Studies, Memorial University. Contribution No. 249 from the Marine Sciences Research Laboratory, Memorial University of Newfoundland     

On the structure of the pulmonate osphradium

Summary The osphradium of Planorbarius consists of a blindly-ending ciliated canal, formed by an infolding of the mantle epithelium, and a basal ganglion of nerve cells which is comparable in complexity with ganglia of the central nervous system. The distribution of cell types in the osphradial epithelium is specialised so that three regions can be recognised; the ciliated, the secretory and the sensory regions. The basal sensory region of the canal epithelium consists of ciliated cells and is innervated by sensory neurones of the osphradial ganglion. The middle secretory region contains mainly of mucus-secreting cells and the epithelium adjacent to the osphradial aperture of ciliated cells and secretory cells of a second type. The sensory neurones of the osphradial ganglion are bipolar or of a modified monopolar type. Other monopolar neurones, similar to those common in the central nervous system are of non-sensory function. The osphradium of Paludina, although of typical prosobranch form, possesses ciliated pits similar to the single canal of Planorbarius, which may indicate a shared modality of receptor function. A definite function cannot be ascribed to the pulmonate osphradium based on morphological evidence alone.     

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.     

The fine structure of the newly discovered propodial ganglia of the veliger larva of the nudibranch Onchidoris bilamellata

Summary Two pairs of ganglia are found in the propodial region of the veliger of Onchidoris bilamellata: the anterolateral pair is located at the foremost corners of the propodium, and the frontal pair is located beside the propodial midline. Both sets of ganglia are positioned below the epidermis, and they are joined to the cerebral ganglia by large, common connectives. Each ganglion possesses sensory cells, nerve cells and sheath cells, and the frontal pair contains a complement of secretory cells. Externally, the propodial ganglia are manifested as sensory fields. The fields of the anterolateral pair are elliptical in shape, and each appears as a band of cilia bordering an unciliated zone. The region devoid of cilia is composed of ordinary epidermal cells, whereas the ciliated portion is comprised of dendritic endings originating from cells in the ganglion. Dendrites arise from one type of sensory cell and pass through the epidermis in bundles. Each dendrite terminates as a single cilium at the epidermal surface. Sensory fields of the frontal ganglia are key-shaped and oppose one another on the anterior end of the foot. Each field appears as a flat, circular, unciliated region which extends into a ciliated groove that runs dorsally toward the mouth. The groove contains the terminals of secretory cells, ciliated sensory cells, and the cell bodies of nonciliated sensory cells. The nonciliated sensory cells, characterized by a microvillous apex, are the dominant cells in the flattened circular zone. The space between the frontal ganglia and the epidermis is bridged by bundles of processes which are similar to those of the anterolateral ganglia. However, these tracts contain collections of the apical processes of secretory cells, the dendrites of ciliated sensory cells, and the axons of nonciliated sensory cells. Morphological and behavioral evidence indicates that the propodial ganglia serve a chemosensory function during settlement and metamorphosis.     

THE STRUCTURE AND DISTRIBUTION OF PERIPHERAL CILIATED RECEPTORS IN THE BIVALVE MOLLUSCS DONAX SERRA AND D. SORDIDUS

The siphons and mantle edge of Donax serra and D. sordidus possesstwo types of ciliated sensory receptor. Type 1 has > 7 ciliawith an exposed length of 0.7–2.4 µm. Type II hasfewer cilia (2–5) which are 2–6 µm long. Athird type (Type III) described from the tips of the tentaclesof the siphon and mantle edge of D. sordidus, possesses twotufts of cilia which are 12 µm long. All three receptortypes appear to be primary receptors. Estimates of abundanceshow that receptors are most numerous on the tips of the siphontentacles (9.75 x 10³. mm^–2), and it is suggested thatthese receptors function as chemoreceptors. (Received 11 May 1983;     

Changes of traits in a bacterial population associated with protozoal predation

In an attempt to understand the significance of predation in the evolution of prey species, the ecological and morphological characteristics of bacterial species under predation by a ciliated protozoa,Cyclidium sp., were investigated. Serial transfer at 7 day intervals was applied to the bacterial populations in the presence or absence ofCyclidium. Although cells of the parental bacterial strain are typically short rods up to 1.5 μm long, cells of much greater length, up to 20 μm long (type L) were found in populations exposed to predation fromCyclidium. However, the wildtype, shorter length bacteria persisted even after the appearance of type L. Type L was not observed in the singl bacterial culture throughout the serial transfers. Type L appeared to improve the ability to escape predation by elongating cell size, but growth rate and saturation density were decreased.     

Regional distribution of three ultrastructural retinula types in the retina of Cataglyphis bicolor Fabr. (Formicidae,Hymenoptera)

Summary The retina of Cataglyphis bicolor was investigated by electron microscopy. Three types of structurally distinct retinulae were found and mapped throughout the compound eye: Type I is composed of four unpigmented thin cells, four larger pigmented cells as well as a basal ninth cell. Its rhabdom possesses a round cross section and four microvilli directions. This type occupies most of the dorsal two-thirds of the retina. Type II consists of two thin cells, two intermediate cells and four large cells. A basal ninth cell is also present; the rhabdom is as in type I. Type II retinulae are located in the ventral third of the retina. Type III ommatidia are unique within the Hymenoptera: there are four large pigmented cells, four thinner unpigmented cells and a basal ninth cell. The rhabdom, however, has a dumb-bell shaped cross section; two small cells lie at its opposed extremities and the remaining six cells have mutually perpendicular microvilli orientations. This type of retinula is found at the dorso-medial eye margin. Serial sectioning in this region revealed a conical shaped rhabdom without any torsion along the longitudinal axis. The rhabdomere cross section was calculated from distal and proximal thin sections. Angular statistics were applied to the microvilli directions of all three ommatidial types to determine the degree of order. A possible functional significance of the structural specializations of the different eye regions is discussed.Supported by Swiss National Science Foundation, Grant No. 3.814.72 awarded to Prof. Dr. R. Wehner. This work is part of a Ph. D. thesis. I wish to thank Prof. Dr. R. Wehner for continuous support and my colleagues Dr. P. Duelli and Dr. E. Meyer for a fruitful collaboration     

THE ULTRASTRUCTURE OF CILIATED CELLS FROM THE SIPHON OF SOLEN CAPENSIS (MOLLUSCA, BIVALVIA)

The structure of ciliated cells from the siphon of Solen capensishas been studied by both scanning and transmission electronmicroscopy. Two types of ciliated cell, based on the numberand length of cilia have been described which resemble thosedescribed in Donax. Type I is characterized by having 26–57({macron}= 43, n = 50) cilia which are 2.5 µm in length;Type II has fewer cilia (5–10; {macron}= 7) which are5 µn long. Both are primary receptors. Estimations ofabundance show that receptors are most numerous on the tipsof the siphon tentacles (8.8 x 10³/mm²). (Received 15 January 1985;     

The structures of the tentacles of Rhabdopleura compacta (Hemichordata) with special reference to neurociliary control

Summary The tentacle of Rhabdopleura compacta (Hemichordata) consists of two layers of cells surrounding a central coelomic cavity. The two layers of cells are separated by a cell free basement lamella.The tentacles on the arms of Rhabdopleura bear three longitudinal rows of cilia. The ciliated cells are closely associated with bundles of nerve fibres, and between some of the cells and nerve fibres there are synapses. The peripheral regions of the ciliated cells are joined to one another by desmosomes. Tonofibrils join some of these desmosomes to the kinetosomes of the cilia.The nerve fibres are confined to the ectodermal layer and the muscle cells to the layer of cells within the basement lamella. In the ectodermal layer besides ciliated cells there are mucus cells, densely pigmented cells, and green bodies. The function of these last two types of cells is secretory. Most of the epithelial cells have microvilli upon their free borders.I wish to thank Professor J. Z. Young F. R. S. for enthusiastic advice and encouragement. Dr. R. Bellairs generously provided the facilities for electron microscopy. Mr. R. Moss gave excellent technical and photographic assistance. Dr. A. Stebbing of the Plymouth Marine Biological Laboratory helped me to obtain and to identify the specimens. Professor D. W. James kindly allowed me to use his facilities for interference microscopy.     

TGFβ1 induces growth arrest and apoptosis but not ciliated cell differentiation in rat tracheal epithelial cell cultures

Summary We are studying the regulation of ciliated cell differentiation using an in vitro model of tracheal regeneration. Previously, we reported that removal of growth stimulating compounds such as epidermal growth factor (EGF) and cholera toxin reduced DNA synthesis and cell number while increasing ciliated cell differentiation (Clark et al., 1995). This result suggested that the induction of growth arrest may stimulate terminal differentiation of airway epithelial cells into ciliated cells. Transforming growth factor βs (TGFβs) inhibit epithelial cell proliferation and have also been shown to stimulate epithelial cell differentiation. In this study, the effect of TGFβ₁ on growth and ciliated cell differentiation of rat tracheal epithelial (RTE) cells was examined. TGFβ₁ inhibited [³H]thymidine incorporation by RTE cells in a dose-dependent manner. A 40% inhibition was observed after a 24-h incubation with 10 pM TGFβ₁. Continuous treatment with TGFβ₁ (1–50 pM) also reduced cell number during the time when ciliogenesis occurs. This reduction resulted in part from a loss of cells through exfoliation, in addition to the inhibition of proliferation. The exfoliated cells exhibited several morphological features characteristic of apoptosis, including shrunken cells, condensed and fragmented nuclei, and intact organelles. In addition, electrophoretic analysis of genomic DNA analysis isolated from exfoliated cells demonstrated the presence of a nucleosomal ladder. However, in contrast to the removal of EGF, treatment with TGFβ₁ for 7 d did not increase ciliated cell differentiation. TGFβ1 is, therefore, capable of inhibiting proliferation and increasing apoptosis in RTE cells without stimulating ciliated cell differentiation.     

Fine Structure of the Female Intoshia variabili(Alexandrov & Sljusarev) (Mesozoa: Orthonectida)

The morphology and fine structure of female Intoshia variabili, new combination for Rhopalura variabiliAlexandrov & Sljusarev, 1992, were studied with transmission electron microscopy. The body surface is covered with a 3-layered cuticula, under which is a layer of ciliated + non-ciliated cells arranged in alternating rings around the body. Ciliated cells have lateral extensions that intercalate with the non-ciliated cells. The kinetosome of each cilium has two longitudinally oriented cross-striated rootlets. The outer surface of the ciliated cells is covered with small tubercles, and the cytoplasm of these cells contains granules, vacuoles, mitochondria, fibrillar structures and lamellary bodies. A band of dense fibrils passes through the upper part of each ring of cells, going from one cell junction to another, encircling the entire body. Between the layer of ciliated + non–ciliated cells and the oocytes, elongated contractile cells from 4–5 longitudinal columns and 1 ring, the latter at the level of ciliated rings 7–9. The contractile cells contain thick and thin longitudinally oriented fibrils. The oocytes contain a large nucleus, numerous mitochondria, electron–dense granules and 1–2 spherical structures. An anteriorly situated, ciliated goblet–like receptor, not described for any other orthonectids, consists of three closely apposed cells, the upper part of which contains densely packed cilia. The genital pore opens through a non–ciliated cell and is surrounded by several cells with granules.     

The lungs of Polypterus senegalus and Erpetoichthys calabaricus: Insights into the structure and functional distribution of the pulmonary epithelial cells

The present article is a comparative, structural study of the lung of Polypterus senegalus and Erpetoichthys calabaricus , two species representative of the two genera that constitute the Polypteriformes. The lung of the two species is an asymmetric, bi‐lobed organ that arises from a slit‐like opening in the ventral side of the pharynx. The wall is organized into layers, being thicker in P. senegalus . The inner epithelium contains ciliated and non‐ciliated bands. The latter constitute the respiratory surface and are wider in E. calabaricus . The air‐blood barrier is thin and uniform in P. senegalus and thicker and irregular in E. calabaricus . In the two species, the ciliated areas contain ciliated cells, mucous cells and cells with lamellar bodies. Additionally, P. senegalus contains polymorphous granular cells (PGCs) and neuroendocrine cells (NECs) while E. calabaricus lacks PGCs but shows granular leukocytes and a different type of NEC. Interestingly, ciliated cells and secretory cells show a dual morphology in E. calabaricus indicating the presence of cellular subtypes and suggesting more complex secretory activity. Also in E. calabaricus , cilia show a novel doublet‐membrane interaction that may control the displacement of the microtubule doublets. The subepithelium is a connective layer that appears thicker in P. senegalus and contains, in the two species, fibroblasts and granulocytes. The outer layer contains bundles of richly innervated striated muscle. This layer is likely involved in the control of lung motion. In the two species, smooth muscle cells constitute a limiting layer between the subepithelium and the striated muscle compartment. The role of this layer is unclear.     

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.     

Morphology of early developing oligodendrocytes in the ventrolateral spinal cord of the chicken

The oligodendroglial population includes Type I and II cells related to several thin axons, Type III cells with a few processes in relation to relatively thick axons and Type IV cells related to a single thick axon. This structural diversity of oligodendrocytes is accompanied by a molecular heterogeneity. In the chicken spinal cord, oligodendrocytes have begun to contact axons at embryonic day (E)10 and compact sheaths have appeared by E12. At the latter stage, most sheath-forming oligodendrocytes contact more than one axon. At E15, however, each sheath-forming cell seems to have developed a Schwann cell-like anatomy, being related to a single axon. Based on these findings, the present study examines more thoroughly the anatomy of early developing oligodendrocytes in the chicken spinal cord. Examination of slices immunostained with antibodies against the oligodendroglial marker O4 showed that a few positive cells are present at E6, after which the occurrence increases with age. At E12 most immunostained cells have two or more processes. At E15 however, dye-injected oligodendrocytes have developed a Type IV structure. Between E12 and E15, mean sheath length increases about 4×, from 50 μm to over 200 μm, while the length of the spinal cord increases 36% only. This indicates that early oligodendrocytes in chicken white matter develop a Type IV anatomy between E12 and E15 through an elimination of sheaths.     

Evolution of larval form in ophiuroids: insights from the metamorphic phenotype of Ophiothrix (Echinodermata: Ophiuroidea)

Comparison of development through metamorphosis in Ophiothrix species provided insights into the evolutionary relationships between Type I (ophiopluteus only) and Type II (ophiopluteus and vitellaria) patterns of development in the Ophiuroidea. As typical of Type I developers, the six inner larval arms in Ophiothrix spongicola were fully resorbed at metamorphosis and no remnants of ciliated epithelia were retained. The postero-lateral arms function as locomotory organs for the developing juvenile and were discarded at settlement. In contrast, in O. ciliaris the epithelia of the inner arms were transformed into ciliated ridges, similar to those seen in vitellariae and the postero-lateral arms were resorbed rather than being discarded. Larval arm resorption in O. ciliaris is similar to that in Type II developers. The metamorphic phenotype of O. ciliaris provides a link between Type I and II development. The presence of two types of metamorphosis in congeneric ophiuroids and the variable metamorphic phenotype of O. ciliaris was unexpected. It appears that closely related ophiuroids and individual species may have the capacity to metamorphose using either Type I or Type II pathways. Although the phylogenetic distribution of metamorphic phenotypes indicates that Type II development may be the ancestral state, comparative morphology suggests that a developmental dichotomy based on larval arm resorption may not be appropriate for the Ophiuroidea. Until metamorphosis is characterized for more taxa, the ancestral developmental mode for the Ophiuroidea will remain a matter of conjecture.     

Fine structure of olfactory epithelium inSchizothoraichthys progastus McClelland andSchizothorax richardsonii Gray (Cyprinidae: Teleostei) from Garhwal Himalaya (India)

The olfactory epithelium of two closely related species of snowtrout—Schizothoraichthys progastus McClelland andSchizothorax richardsonii Gray (Subfamily: Schizothoracinae. family-Cyprinidae, Teleostei), from a perennial glacier-fed river Mandakini of Garhwal hills was studied by employing transmission electron microscopic method The olfactory lamella comprises two epithelia—anterior and posterior, with a stroma sandwiched in between. Both are strartified. The anterior one is thicker than posterior. InSchizothoraichithys progastus, the sensory part of epithelium has two types of receptor cells—ciliated receptor cells and rod cells whilst inSchizothorax richardsonii, there arc three types of receptor cells—ciliated receptor cells, microvillous receptor cells and rod cells in addition to sustentacular cells, basal cells and mucous cells. While inhabiting similar hillstream habitat, the differential ecological niches, feeding habits etc., account for the presence of different receptor cell types in these species, It implies the possible diversification at cellular and physiological levels so as to minimize the competition by using varied olfactory cues.