- Research article
- Open Access
Olfactory and solitary chemosensory cells: two different chemosensory systems in the nasal cavity of the American alligator, Alligator mississippiensis
© Hansen; licensee BioMed Central Ltd. 2007
- Received: 19 December 2006
- Accepted: 03 August 2007
- Published: 03 August 2007
The nasal cavity of all vertebrates houses multiple chemosensors, either innervated by the Ist (olfactory) or the Vth (trigeminal) cranial nerve. Various types of receptor cells are present, either segregated in different compartments (e.g. in rodents) or mingled in one epithelium (e.g. fish). In addition, solitary chemosensory cells have been reported for several species. Alligators which seek their prey both above and under water have only one nasal compartment. Information about their olfactory epithelium is limited. Since alligators seem to detect both volatile and water-soluble odour cues, I tested whether different sensory cell types are present in the olfactory epithelium.
Electron microscopy and immunocytochemistry were used to examine the sensory epithelium of the nasal cavity of the American alligator. Almost the entire nasal cavity is lined with olfactory (sensory) epithelium. Two types of olfactory sensory neurons are present. Both types bear cilia as well as microvilli at their apical endings and express the typical markers for olfactory neurons. The density of these olfactory neurons varies along the nasal cavity. In addition, solitary chemosensory cells innervated by trigeminal nerve fibres, are intermingled with olfactory sensory neurons. Solitary chemosensory cells express components of the PLC-transduction cascade found in solitary chemosensory cells in rodents.
The nasal cavity of the American alligator contains two different chemosensory systems incorporated in the same sensory epithelium: the olfactory system proper and solitary chemosensory cells. The olfactory system contains two morphological distinct types of ciliated olfactory receptor neurons.
- Nasal Cavity
- Olfactory Epithelium
- Olfactory System
- Apical Ending
- Olfactory Receptor Neuron
The nasal cavity of all vertebrates houses multiple chemosensors. The olfactory and the vomeronasal receptors detect a variety of odours including food-related and social signals. In addition, chemically-sensitive free nerve endings of the trigeminal nerve and trigeminally innervated chemosensors that respond to irritants have been reported for some vertebrate species. The chemosensors are expressed in various cell types. In mammals, the olfactory system contains ciliated and microvillous olfactory receptor neurons (OSNs). In many mammals these neurons are segregated in two compartments: ciliated OSNs are housed in the main olfactory epithelium detecting chemicals related mostly to food and microvillous OSNs in the so-called vomeronasal organ (VNO) detecting mostly (but not limited to) social cues . Fish olfactory epithelium also contains ciliated and microvillous OSNs , but here both cell types are intermingled in one olfactory epithelium since fish do not have a VNO. In mammals as well as in fish, both ciliated and microvillous OSNs utilize characteristic G-proteins in their transduction cascade: Gαolf is present in ciliated OSNs; Gαi, Gαo and/or Gαq are present in microvillous OSNs [3–7].
Chemoreception in semi-aquatic animals is interesting per se since both volatile and water-soluble compounds have to be detected in two different environments. Most semi-aquatic reptiles (turtles, tortoises, snakes) and amphibians possess a VNO lined with microvillous OSNs as well as the main olfactory chamber [8–11]. Turtles employ the main olfactory epithelium and the VNO to detect air-borne and/or water-soluble chemicals. However, this compartmentalization does not lead to a strict separation of volatile and soluble odorants. The VNO of semi-aquatic turtles responds to both volatile and non-volatile odorants . Female tree frogs can detect aquatic sex pheromones from male frogs . Axolotls (Ambystoma mexicanum) use their olfactory and vomeronasal systems equally to detect social cues from conspecifics . The olfactory system of Triturus pyrrhogaster, changes morphologically and physiologically when the animals are kept either in a terrestrial or an aquatic environment [15, 16].
Information about the nasal cavity of crocodilians is limited (for early macroscopic studies see ). This is not surprising given the difficulty of obtaining and handling the specimens. On the other hand, chemoreception in crocodilians (comprising the three families: Alligatoridae, Crocodylidae, and Gavialidae) is especially interesting since they hunt both in terrestrial and in aquatic surroundings. Crocodilians have only one olfactory chamber [18, 19]. A VNO is absent in the adult animals. Thus, at first glance, crocodilians seem to have only one olfactory system comprising the main olfactory chamber and what type(s) of OSNs are present in the olfactory epithelium is unknown. Also, little is known about how crocodilians use their olfactory system. Neill  reported that the American alligator detects blood in the water. Behavioural and olfactometer experiments suggest that crocodilians detect both air-borne and water-soluble chemicals and use their olfactory system for hunting . When above water, crocodilians enhance their ability to detect volatile odorants by gular pumping, a rhythmic movement of the floor of the pharynx [21, 11, 22]. If crocodilians do not have two different nasal compartments but detect both air-borne and water-soluble chemicals: do they have different types of olfactory neurons?
Also of interest is whether crocodilians possess trigeminally innervated solitary chemosensory cells (SCCs). These are specialized cells that have been described for anamniote vertebrates including hagfish , teleosts and amphibians [24–26]. SCCs, which are modified epithelial cells, represent a separate chemosensory system without a specific endorgan. These secondary receptor cells, i.e. lacking an axon, are scattered in different epithelia (e.g. skin, oropharyngeal cavity, nasal cavity, gills) and detect various chemical substances depending on the species investigated. These cells are scarce, and since they are scattered in the epithelium as single cells, no cell counts exist except for few fish species  and rats . SCCs are also present in the nasal cavity and the respiratory tract of rodents where they detect irritants [28, 29]. In rodents, SCCs express T2R "bitter-taste" receptors and α-gustducin, a G-protein involved in chemosensory transduction as well as phospholipase β2 (PLCβ2), a downstream component of the T2R-gustducin transduction cascade. Peptidergic fibres (containing Substance P/calcitonin gene-related peptide CGRP) of the trigeminal nerve form synaptic contacts with these cells . Given the different origin and different innervation and transduction pathway of these receptor cells, it is obvious that SCCs represent a chemosensory system different from that of olfaction.
SCCs have also been reported for the oral and nasal cavity of cows  and the nasal epithelia of humans  but it is unclear whether the SCCs of mammals are related to the SCCs of anamniote vertebrates. The presence of similar SCCs in a reptile would support phylogenetic continuity rather than convergence between the anamniote and mammalian groups, suggesting that the SCCs are homologous throughout the vertebrate lineage.
The present study is the first to utilize electron microscopy and immunocytochemistry to examine the peripheral olfactory organ of a crocodilian, the American alligator Alligator mississipiensis. The study focussed on two questions: (1) What are the cell types in the nasal epithelium and does their ultrastructure and/or distribution give any clues regarding the differences between olfaction above or under water? Scanning and transmission electron microscopy was utilized to describe the cell types present. Furthermore, immunocytochemical tests with markers typically used for olfactory neurons were applied. (2) Do alligators possess solitary chemosensory cells (SCCs) thus suggesting that this chemosensory system is a conserved trait in the vertebrate lineage? The criteria for identifying SCCs were twofold: 1) morphology and 2) immunoreactivity to markers for SCCs. SCCs previously found in various vertebrates showed similarities in terms of cell shape and cell organelles. The cells are spindle-shaped with an apical ending that bears either one big villus or few smaller villi. At the surface of the epithelium, the apical ending is often constricted into a "neck". The cell body is filled with abundant vesicles of different shape and size [25, 32, 28]. A marker for the transduction pathway of SCCs is PLCβ2 [28, 31, 29]. Since SCCs are secondary receptor cells they are contacted by nerve fibres and these are immunoreactive for CGRP or Substance P.
Overall Organization and Histology
Olfactory sensory neurons
The description of the ultrastructure of the OSNs follows the criteria commonly used for olfactory epithelium. As mentioned above, receptor cells are categorized macroscopically by their height within the epithelium. At the ultrastructural level, cell organelles are used to categorize OSNs, e.g. structural features of the cilia, presence or absence of rootlets, "checker-board" pattern of chromatin in nuclei, longitudinally arranged mitochondria, presence or absence of centrioles [35, 36]. Electron micrographs (TEM) show that in the pseudostratified epithelium, the supporting cells are the most prominent (Fig. 3A). Their nuclei lie above the level of nuclei of OSNs. Abundant clear vesicles ca. 0.6 to 1.0 μm in diameter, fill the area above the nucleus and the most apical area leaving a small portion in between for mitochondria and electron-dense cytoplasm (Fig. 3A,B). Occasionally centrioles (usually two) are present in the upper portion of the cell which is devoid of vesicles (not shown). At the surface bordering the lumen, the width of the supporting cells ranges from 2.8 to 4.1 μm. This is only a rough estimate since these cells often envelop the OSNs. Consequently, at the ultrastructural level two supporting cell profiles, one on each side of an OSN, can be the same cell seen twice. The surface of the supporting cells is covered with numerous microvilli, about 4 to 5 μm long and 0.08 to 0.17 μm wide (Figs. 3B, 4C, 5A–C). OSNs are dispersed between the supporting cells (Figs. 3, 4A, 5C,D); the width of their apical dendrites (1 to 1.4 μm) is even smaller than the upper portion of the supporting cells. As seen in the scanning electron microscope (SEM), the pronounced olfactory knob bears about 6 to 7 cilia (10 to 15 μm long, approx. 0.3 μm wide) that do not taper at their end. In addition, the olfactory knobs bear several thin microvilli (about 1 μm long), and thus shorter and smaller than those of the supporting cells (Figs. 3B–D, 4A). Some TEM sections suggest the presence of OSNs with only microvilli. However, serial sections reveal that this is misleading (Figs. 3C, 4A), since the original plane of section may not include all of the cilia. All OSNs seen in serial ultrathin sections were so-called mixed receptor cells (bearing both cilia and microvilli) as described for birds by Graziadei . Nevertheless, based on dendritic morphology, two different types of OSNs do exist. The distribution of these two types of OSNs within the nasal cavity has no obvious pattern. The olfactory knobs of both OSN types contain small light vesicles. Rootlets are absent from cilia of both cell types (Fig. 3B–D). Although both types bear cilia and microvilli on their olfactory knobs, their dendrites show different features. Type I OSNs are relatively electron-lucent and contain small vesicles (70–100 nm) and few microtubules. A few mitochondria are arranged longitudinally (Fig. 3B). Beneath the olfactory knob – often even deep in the dendrite – several centrioles are present (Fig. 4A), a feature that never occurred in the second OSN type. The cytoplasm of the type II OSN is electron-dense and filled with abundant mitochondria that sometimes reach into the olfactory knob. Their cytoplasm is electron-dense (Fig. 3B,C,D). Centrioles are lacking.
Beneath the layer of OSNs a layer of basal cells occurs. Basal cells rest on the basal lamina, their shape often following the curves of the basal lamina (Fig. 4B). Within the olfactory epithelium a few cells occur that contain cell debris enveloped in large vesicles (Fig. 4D). The nature of these presumably phagocytotic cells is unknown.
Strictly non-olfactory areas of epithelium are confined to the most ventral areas of the nasal cavity and small areas in the folding of the turbinates. These non-olfactory areas are mostly lined with columnar epithelial cells. They bear either tiny microvillous-like protrusions (Fig. 4E) or numerous cilia (Fig. 5E) which unlike cilia present on sensory neurons have pronounced rootlets extending into the cell (arrowheads Fig. 4D). Some of the microvilli-bearing cells are of mucous character (compare ) containing dark, electron-dense vesicles of various sizes. This part of the epithelium is loosely-packed and the wide interstitium is filled with dense extracellular matrix (Fig. 4E).
The antisera that worked in the alligator tissue corroborated the results obtained at the electron microscopic level.
(3) YOL 1/34 tubulin (a marker for microtubules) immunoreaction is present in cilia (Fig. 8C) and in fibres coursing below the olfactory epithelium but no positive fibres are seen beneath the nonsensory areas.
Solitary chemosensory cells
Occasionally, cells with the morphology of solitary chemosensory cells (SCCs) occur in the olfactory epithelium. These cells are scarce but stand out in SEM and TEM preparations (Figs. 4C, 5F). Their apical ending is dome-shaped. Supporting cells seem to indent into the upper part of the cell resulting in a "neck" of the presumed SCCs (Fig. 4C). The dome is filled with dense cytoplasm and few tiny vesicles (approx. 0.02 – 0.05 μm). The area below the "neck" on the other hand contains abundant slightly larger vesicles (approx. 0.07 – 0.2 μm).
Immunocytochemical results (synapses in the lower portion of the epithelium, PLCβ2 in apical endings) corroborate the notion that these cells are, indeed, SCCs.
(2) Substance P labels nerve fibres under the nasal epithelium. Some of the fibres reach into the olfactory and into the nonsensory epithelium (Fig. 8D). Other Substance P-positive fibres are present in the close vicinity of the glands.
The present study is the first to utilize electron-microscopic and immunocytological methods on the olfactory epithelium of a crocodilian species. The findings show that almost the entire nasal cavity is lined with olfactory (= sensory) epithelium, but the density of the olfactory receptor neurons (OSNs) varies along the nasal cavity. Two different types of ciliated OSN exist that vary in cell organelles and electron-density. The nasal cavity contains not only olfactory sensory neurons (OSNs), but also receptor cells of a second chemosensory system: the solitary chemosensory cells (SCCs) which connect to peripheral fibres of the trigeminal nerve.
Early studies on crocodilians focused on the macroscopic morphology of the head and described the nasal cavity only briefly and mostly in terms of head morphology (for a more complete literature list on head morphology see . Saint Girons  investigated the nasal cavities of Crocodylus niloticus and Caiman crocodilus with histological methods.
Olfactory sensory neurons
The present study of the American alligator confirms Saint Girons'  findings insofar as almost the entire nasal cavity is lined with olfactory (= sensory) epithelium. However, the density of OSNs is heterogeneous along the nasal cavity of the American alligator. The highest numbers of OSNs occur in the zones of the two turbinates and the lowest numbers close to the naris. Saint Girons'  cell countings in histologically stained sections rendered a proportion of 61% OSNs for Crocodylus and 59% of OSNs for Caiman. These results are very different from what I counted in electron microscopic experiments: In the alligator, the proportion of OSNs versus supporting cells is reversed compared to Saint Girons' countings : the olfactory epithelium contains many more supporting cells than OSNs – even in the turbinate zones where the OSNs have the highest density (Fig. 6). The difficulties in counting supporting cells cannot account for this considerable difference. This could be species-dependent but it is more likely due to the very different techniques. Saint Girons  counted nuclei in histologically stained thick sections which is tedious but not very reliable due to the poor resolution and thus difficulties in distinguishing cell types, whereas in the present study cells were counted at the ultrastructural level.
Since alligators hunt above and under water and given the fact that they possess only one nasal compartment the question arises how are volatile and/or water-soluble chemicals detected? A study on the semi-aquatic newt Triturus pyrrhogaster reported a change of morphology and physiological properties of the OSNs depending on the environment. In a terrestrial environment the cilia of the OSNs grew longer than when they were in aquatic surroundings. Slow potentials evoked in the olfactory epithelium changed from responding to odorous fluids in an aqueous medium to responding to odorous vapours in a terrestrial environment . Interestingly, two types of OSNs are present in the olfactory epithelium of the American alligator. Both types bear cilia that do not taper at their ends as seen in rodents. Other than that, the two types of ciliated OSNs show different morphological features that are commonly used to describe OSNs (number of mitochondria, presence/absence of centrioles, electron density of cytoplasm ) so that type I and type II OSNs are easily distinguished at the ultrastructural level. This has not been reported for birds (the second group of the Sauropsida) or other reptiles. What the two different types of OSNs mean in terms of function is yet unknown, but it is tempting to speculate that one type of OSN may be utilized above water for air-borne stimuli while the other is used under water. The results described in this study were collected from juvenile specimens. It remains to be shown whether the findings also apply to fully mature alligators.
Immunocytochemical experiments were hampered by the fact that most of the antisera made for rodents do not work in alligators. Nevertheless, it was possible to show that, as seen in fish and mammals, the OSNs in alligators express Gαolf, the most common G-protein subunit in olfactory transduction [3, 6, 7]. The neuronal marker PGP9.5 confirmed the presence of OSNs in various areas. This was especially helpful since it corroborated on a larger scale what ultrastructural experiments had shown: (a) that the density of OSNs varies from the anterior end of the snout to the turbinates, and (b) that the height of the epithelium is not correlated to the presence/absence of OSNs. They occur in thicker as well as in thinner areas of epithelium. These two features were also evident in experiments with the YOL 1/34 antibody, a marker for tubulin in cilia, and Gαolf.
Solitary chemosensory cells
Another interesting feature of the alligator's nasal epithelium is the presence of SCCs. These chemoreceptor cells had been known for fish and amphibians [24, 25]. They occur in the skin of the body of fish, in the oral cavity and on the gills [26, 39]. In the alligator, SCCs are integrated into the olfactory epithelium, a feature that up to now has been reported only for the goldfish olfactory epithelium . With some exceptions, their function is not well understood. Recently, SCCs were also described for rodents . In this case, the SCCs are located in the respiratory epithelium of the nasal cavity. In rodents, the SCCs express components of the T2R transduction cascade including gustducin and PLCβ2. Electrophysiological and behavioural experiments led to the conclusion that SCCs in rodents serve as "sentinels" in the anterior nasal cavity guarding against potentially harmful or irritant chemicals. SCCs also occur in guinea pigs  and cows . In alligators, dome-shaped apical endings were labelled with PLCβ2 as are nasal SCCs in rodents. In addition, Substance P-positive fibres were present in and under the nasal epithelium of the alligator indicating innervation of the SCCs by trigeminal nerve fibres as seen in rodents. The presence of SCCs in alligators as well as in hagfish , elasmobranchs, teleost fish , amphibians [24, 42], rodents , large mammals , and humans  support the notion that SCCs are an evolutionarily conserved trait having evolved early in vertebrate phylogeny.
Two different chemosensory systems are incorporated in the olfactory epithelium: olfactory sensory neurons proper and solitary chemosensory cells comprised of secondary sensory cells innervated by the trigeminal nerve. Almost the entire nasal cavity of the American alligator is lined with olfactory (sensory) epithelium. Two morphologically distinct types of ciliated OSNs are present. Although both types bear cilia as well as microvilli on their olfactory knobs, they differ in electron density and cell organelles. The density of OSNs varies with the lowest numbers close to the nares and the highest numbers on the turbinates. OSNs as well as SCCs in alligators express members of the transduction cascade seen in rodents. The occurrence of SCCs in the alligator suggests phylogenetic continuity of this cell type throughout the vertebrates.
Three juvenile alligator heads (Fig. 1A) fixed in 4% paraformaldehyde (kindly provided by Dres. Catherine Carr and Daphne Soares, University of Maryland) were split at the midline by means of a fretsaw (Fig. 1B). The complete nasal sacs were dissected out and divided into 5 zones for further processing (Fig. 1C). Two animals were used for transmission electron microscopy and immunocytochemistry, the third animal for scanning electron microscopy and immunocytochemistry.
For an overview at the light microscopic level, cryosections (16 μm) were treated with the histological staining Kernechtrot-Lichtgrün-Orange (KLO) (0.1% nuclear red – C.I. 60760, Merck, Darmstadt – in 5% aluminium sulphate followed by 0.2% light green – C.I. 42095, Allied Chemical Corp., New York, 1% orange G – C.I. 16230, Allied Chemical Corp., New York – and 0.5% phosphotungstic acid in 1% acidic acid) . Briefly, the slides were washed in dH2O, immersed in a mixture of nuclear red in aluminium sulphate for 10 min, washed in dH2O, and immersed in a mixture of light green and orange G in phosphotungstic acid for 1 – 2 min. After the staining process, the slides were dehydrated in ethanol and xylene. Epon-Araldite-embedded pieces of tissue were cut at 1 μm and stained with 1% toluidin blue (J. T. Baker Chemical Co., Phillipsburg).
Scanning electron microscopy (SEM)
Pieces of tissue of all 5 zones of the nasal cavity were postfixed in 4% glutaraldehyde in 0.05 M phosphate buffer (pH 7.2). After rinsing in phosphate buffer, the specimens were dehydrated in a graded series of acetone and isoamyl acetate, critical-point-dried in CO2, coated with gold, and examined with a LEO 1525 scanning electron microscope (Carl Zeiss, Jena, Germany).
Transmission electron microscopy (TEM)
Pieces of tissue of all 5 zones of the nasal cavity were postfixed in 4% glutaraldehyde in 0.05 M phosphate buffer (pH 7.2) for several hours. After rinsing in phosphate buffer, the tissue samples were postfixed with 1% osmium tetroxide for 2 h. The fixed specimens were dehydrated in a graded series of ethanol and acetone and embedded in Epon-Araldite (Electron Microscopy Sciences, Hatfield, PA). Ultrathin sections (silver to gold) were stained with uranyl acetate and lead citrate and examined with a FEI Tecnai G2 electron microscope (Philips, Eindhoven, Netherlands).
Epithelia of all 5 zones were photographed in the transmission electron microscope and printed at a magnification of 4000×, the lowest magnification where it was possible to unequivocally distinguish cell types. Photos of each zone were taken in a single session to ensure that the epithelia were captured only once. Thus, double counting of cells was prevented. On these photos, the apical portion of the epithelium was divided into sections (87 in total) each representing 25 μm of actual tissue. Only OSNs that reached the apical surface were counted. The investigator was blinded as to location of the sample at the time each was counted. Statistical analysis (ANOVA, Tukey test) was done with the program SPSS 15.0 (SPSS Inc., Chicago).
Antisera used for immunocytochemistry
Thanks are due to Miss Renate Walter, Zoological Institute, University of Hamburg, for her expert help with the scanning electron microscope, to Catherine Carr and Daphne Soares (University of Maryland) for providing the alligator heads, and to Thomas E. Finger (University of Colorado) for helpful comments on this manuscript and Marco Tatangelo (University of Michigan) for help with the statistics. The study was supported by grants NIDCD DC-06070 to T. E. Finger, DC-04657 to Diego Restrepo, and DC-007732-01 to A.H.
- Farbman AI: Cell Biology of Olfaction. 1992, Cambridge University PressGoogle Scholar
- Bannister LH: The fine structure of the olfactory surface of teleostean fishes. Quart J Microsc Sci. 1965, 106: 333-342.Google Scholar
- Jones DT, Reed RR: Golf: an olfactory neuron specific-G protein involved in odorant signal transduction. Science. 1989, 244: 790-795. 10.1126/science.2499043.PubMedView ArticleGoogle Scholar
- Wekesa KS, Anholt RRH: Differential expression of G proteins in the mouse olfactory system. Brain Res. 1999, 837: 117-126. 10.1016/S0006-8993(99)01630-3.PubMedView ArticleGoogle Scholar
- Wekesa KS, Miller S, Napier A: Involvement of Gq/11 in signal transduction in the mammalian vomeronasal organ. J Exp Biol. 2003, 206: 827-832. 10.1242/jeb.00174.PubMedView ArticleGoogle Scholar
- Hansen A, Rolen SH, Anderson KT, Morita Y, Caprio J, Finger TE: Correlation between olfactory receptor cell type and function in the channel catfish. J Neurosci. 2003, 23: 9328-9339.PubMedGoogle Scholar
- Hansen A, Anderson KT, Finger TE: Differential distribution of olfactory receptor neurons in goldfish: structural and molecular correlates. J Comp Neurol. 2004, 477: 347-359. 10.1002/cne.20202.PubMedView ArticleGoogle Scholar
- Hatanaka T, Matsuzaki O, Shibuya T: Fine structure of vomeronasal receptor cells in the Reeve's turtle, Geoclemys reevesii. Zool Mag. 1982, 91: 190-193.Google Scholar
- Hansen A, Reiss JO, Gentry CL, Burd GD: Ultrastructure of the olfactory organ in the clawed frog, Xenopus laevis, during larval development and metamorphosis. J Comp Neurol. 1998, 398: 273-288. 10.1002/(SICI)1096-9861(19980824)398:2<273::AID-CNE8>3.0.CO;2-Y.PubMedView ArticleGoogle Scholar
- Reiss JO, Eisthen HL: Chemical Senses: comparative anatomy and physiology in amphibians. Senses on the Threshold, J G H Thewissen, S Nummela (eds ), University of California Press, Berkeley. 2007.Google Scholar
- Halpern M, Martinez-Marcos A: Structure and function of the vomeronasal system: an update. Progr Neurobiol. 2003, 70: 245-318. 10.1016/S0301-0082(03)00103-5.View ArticleGoogle Scholar
- Hatanaka T, Matsuzaki O: Odor responses of the vomeronasal system in Reeve's turtle, Geoclemys reevesii. Brain, Behav Evol. 1993, 41: 183-186.View ArticleGoogle Scholar
- Wabnitz PA, Bowie JH, Tyler MJ, Wallace JC, Smith BP: Aquatic sex pheromone from a male tree frog. Nature. 1999, 401: 444-445. 10.1038/46724.PubMedView ArticleGoogle Scholar
- Park D, McGuire JM, Majchrzak JM, Ziobro JM, Eisthen HL: Discrimination of conspecific sex and reproductive condition using chemical cues in axolotls (Ambystoma mexicanum). J Comp Physiol A. 2004, 190: 415-427. 10.1007/s00359-004-0510-y.View ArticleGoogle Scholar
- Matthes E: Der Einfluss des Mediumwechsels auf das Geruchsvermögen von Triton. Z vergl Physiol. 1927, 5: 83-166. 10.1007/BF00340817.View ArticleGoogle Scholar
- Shibuya T, Takagi SF: Electrical response and growth of olfactory cilia of the olfactory epithelium of the newt in water and on land. J Gen Physiol. 1963, 47: 71-82. 10.1085/jgp.47.1.71.PubMedPubMed CentralView ArticleGoogle Scholar
- Bertau M: Zur Entwicklungsgeschichte des Geruchsorgans der Krokodile. Z Anat EntwGesch. 1935, 104: 168-202. 10.1007/BF02146110.View ArticleGoogle Scholar
- Weldon PJ, Swenson DJ, Olson JK, Brinkmeier WG: The American alligator detects food chemicals in aquatic and terrestrial environments. Ethology. 1990, 85: 191-198.View ArticleGoogle Scholar
- Saint Girons H: Données histologiques sur les fosses nasales et leurs annexes chez Crocodylus niloticus Laurenti et Caiman crocodilus (Linnaeus) (Reptilia, Crocodylidae). Zoomorphologie. 1976, 84: 301-318. 10.1007/BF01578698.View ArticleGoogle Scholar
- Neill WT: The Last of the Ruling Reptiles: Alligators, Crocodiles, and Their Kin. 1971, New York, Columbia University PressGoogle Scholar
- Gans C, Clark B: Studies on ventilation of Caiman crocodilus (Crocodilia: Reptilia). Respir Physiol. 1976, 26: 285-301. 10.1016/0034-5687(76)90001-3.PubMedView ArticleGoogle Scholar
- Putterill JF, Soley JT: Morphology of the gular valve of the Nile crocodile, Crocodylus niloticus (Laurenti, 1768). J Morphol. 2006, 267: 924-939. 10.1002/jmor.10448.PubMedView ArticleGoogle Scholar
- Braun CB, Northcutt RG: Cutaneous exteroreceptors and their innervation in hagfishes. The Biology of Hagfishes. Edited by: Jørgenson JM, Lomholt JP, Weber RE and Malte H. 1998, London, Chapman and Hall, 512-532.View ArticleGoogle Scholar
- Morrill AD: The pectoral appendages of Prionotus and their innervation. J Morphol. 1895, 11: 177-192. 10.1002/jmor.1050110105.View ArticleGoogle Scholar
- Whitear M: Presumed sensory cells in fish epidermis. Nature. 1965, 208: 703-704. 10.1038/208703b0.View ArticleGoogle Scholar
- Kotrschal K, Krautgartner WD, Hansen A: Ontogeny of the solitary chemosensory cells in the zebrafish, Danio rerio. Chem Senses. 1997, 22: 111-118. 10.1093/chemse/22.2.111.PubMedView ArticleGoogle Scholar
- Kotrschal K: Quantitative scanning electron microscopy of solitary chemoreceptor cells in cyprinids and other teleosts. Environ Biol Fishes. 1992, 35: 273-282. 10.1007/BF00001894.View ArticleGoogle Scholar
- Finger TE, Böttger B, Hansen A, Anderson KT, Alimohammadi H, Silver WL: Solitary chemoreceptor cells in the nasal cavity serve as sentinels of respiration. PNAS. 2003, 100: 8981-8986. 10.1073/pnas.1531172100.PubMedPubMed CentralView ArticleGoogle Scholar
- Merigo F, Benati D, Tizzano M, Osculati F, Sbarbati A: α-Gustducin immunoreactivity in the airways. Cell Tissue Res. 2005, 319: 211-219. 10.1007/s00441-004-1007-2.PubMedView ArticleGoogle Scholar
- Tizzano M, Merigo F, Sbarbati A: Evidence of solitary chemosensory cells in a large mammal: the diffuse chemosensory system in Bos taurus airways. J Anat. 2006, 209: 333-337. 10.1111/j.1469-7580.2006.00617.x.PubMedPubMed CentralView ArticleGoogle Scholar
- Hansen A: Unconventional receptor cells in the nasal cavity of humans and rodents. Soc Neurosci Abstr. 2005, 613.19.Google Scholar
- Hansen A: The system of solitary chemosensory cells. Fish Chemosenses. Edited by: Kapoor BG and Reutter K. 2005, New Delhi, Oxford and IBH Publ. Co., 165-176.Google Scholar
- Romeis B: Mikroskopische Technik. Edited by: Böck P. 1989, München, Wien, Baltimore, Urban und Schwarzenberg, 1-697.Google Scholar
- Morita Y, Finger TE: Differential projections of ciliated and microvillous olfactory receptor cells in the catfish, Ictalurus punctatus. J Comp Neurol. 1998, 398: 539-550. 10.1002/(SICI)1096-9861(19980907)398:4<539::AID-CNE6>3.0.CO;2-3.PubMedView ArticleGoogle Scholar
- Hansen A, Zielinski BS: Diversity in the olfactory epithelium of bony fishes: development, lamellar arrangement, sensory neuron cell types and transduction components. J Neurocytol. 2005, 34: 183-208. 10.1007/s11068-005-8353-1.PubMedView ArticleGoogle Scholar
- Graziadei PPC, Monti-Graziadei GA: Olfactory epithelium of Necturus maculosus and Ambystoma tigrinum. J Neurocytol. 1976, 5: 11-32. 10.1007/BF01176180.PubMedView ArticleGoogle Scholar
- Graziadei PC, Bannister LH: Some observations on the fine structure of the olfactory epithelium in the domestic duck. Z Zellforsch. 1967, 80: 220-228. 10.1007/BF00337458.PubMedView ArticleGoogle Scholar
- Lin W, Arellano J, Slotnick B, Restrepo D: Odors detected by mice deficient in cyclic nucleotide-gated channel subunit A2 stimulate the main olfactory system. J Neurosci. 2004, 24: 3703-3710. 10.1523/JNEUROSCI.0188-04.2004.PubMedView ArticleGoogle Scholar
- Finger TE: Evolution of taste and solitary chemoreceptor cell systems. Brain Behav Evol. 1997, 50: 234-243.PubMedView ArticleGoogle Scholar
- Hansen A, Zippel HP, Sorensen PW, Caprio J: Ultrastructure of the olfactory epithelium in intact, axotomized, and bulbectomized goldfish, Carassius auratus. Microsc Res Techn. 1999, 45: 325-338. 10.1002/(SICI)1097-0029(19990515/01)45:4/5<325::AID-JEMT16>3.0.CO;2-V.View ArticleGoogle Scholar
- Taylor-Clark TE, Kollarik M, MacGlashan DW, Undem BJ: Nasal sensory nerve populations responding to histamine and capsaicin. J Allergy Clin Immunol. 2005, 116: 1282-1288. 10.1016/j.jaci.2005.08.043.PubMedView ArticleGoogle Scholar
- Fox H, Lane EB, Whitear M: Sensory nerve endings and receptors in fish and amphibians. The Skin of Vertebrates. Edited by: Spearman RIC and Riley PA. 1980, London, Academic Press, 271-281.Google Scholar
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