- Open Access
Functional neuroanatomy of the rhinophore of Aplysia punctata
© Wertz et al; licensee BioMed Central Ltd. 2006
- Received: 10 March 2006
- Accepted: 06 April 2006
- Published: 06 April 2006
For marine snails, olfaction represents a crucial sensory modality for long-distance reception, as auditory and visual information is limited. The posterior tentacle of Aplysia, the rhinophore, is a chemosensory organ and several behavioural studies showed that the rhinophores can detect pheromones, initiate orientation and locomotion toward food. However the functional neuroanatomy of the rhinophore is not yet clear. Here we apply serotonin-immunohistochemistry and fluorescent markers in combination with confocal microscopy as well as optical recording techniques to elucidate the structure and function of the rhinophore of the sea slug Aplysia punctata.
With anatomical techniques an overview of the neuroanatomical organization of the rhinophore is presented. Labelling with propidium iodide revealed one layer of cell nuclei in the sensory epithelium and densely packed cell nuclei beneath the groove of the rhinophore, which extends to about two third of the total length of the rhinophore. Serotonin immunoreactivity was found within the olfactory glomeruli underneath the epithelium as well as in the rhinophore ganglion. Retrograde tracing from the rhinophore ganglion with 4-(4-(dihexadecylamino)styryl)-N-methylpyridinium iodide (DiA) demonstrated the connection of glomeruli with the ganglion. Around 36 glomeruli (mean diameter 49 μm) were counted in a single rhinophore. Fluorimetric measurements of intracellular Ca2+ levels using Fura-2 AM loading revealed Ca2+-responses within the rhinophore ganglion to stimulation with amino acids. Bath application of different amino acids revealed differential responses at different positions within the rhinophore ganglion.
Our neuroanatomical study revealed the number and position of glomeruli in the rhinophore and the rhinophore ganglion as processing stage of sensory information. Serotonin-immunoreactive processes were found extensively within the rhinophore, but was not detected within any peripheral cell body. Amino acids were used as olfactory stimuli in optical recordings and induced sensory responses in the rhinophore ganglion. The complexity of changes in intracellular Ca2+-levels indicates, that processing of odour information takes place within the rhinophore ganglion. Our neuroanatomical and functional studies of the rhinophore open up a new avenue to analyze the olfactory system in Aplysia.
- Sensory Epithelium
- Olfactory Stimulus
- Projection Pattern
Chemical signal perception represent an important part of communication and is used by a large variety of organisms from protozoans  and yeast  to insects , molluscs [4, 5], fish , mammals  and humans . Sea slugs of the genus Aplysia have been investigated intensively with respect to behavioural and neurobiological studies, and the gill withdrawal reflex has become a well known neuronal model circuit for studies of the cellular basis of learning and memory [9–11]. Fewer studies have targeted the olfactory system of Aplysia [12–14]. In Aplysia, chemosensation plays an important role in the context of various behaviours, e.g. localization of food [14, 15] and sexual behaviour . The rhinophore is considered as the olfactory organ in Aplysia  and was suggested to be important for the detection of pheromones [16, 17]; different peptide-pheromones were identified in the genus Aplysia [4, 18, 19]. Recently, it could be demonstrated that secondary metabolites (alkaloids) from marine sponges stimulate neurons in the rhinophore ganglion of the rhinophore of Aplysia punctata .
Despite biological significance of olfaction, little is known about structural and functional aspects of the olfactory sensory pathway in Aplysia. The neuroanatomy of the tentacle was investigated in the terrestrial snail Achatina , which belong to the group of Pulmonata and to stylommatophoran snails. The tentacles of Achatina fulica contain a tentacle ganglion, glomeruli and four pathways for the projection of olfactory sensory neurons were described. Aplysia was shown to posses a rhinophore ganglion but in contrast to Achatina the eye is at the base and not at the top of the rhinophore, and photoreceptors are located in the rhinophore epithelium [21–24]. In Phestilla sibogae the presence of serotonin, dopamine and norepinephrine in the rhinophores was confirmed , possibly revealing glomerulus-like structures along the olfactory pathway . Serotonin-immunoreactive elements were also found in the rhinophores of Pleurobranchea californica and Tritonia diomedea . Phestilla sibogae, Pleurobranchea californica and Tritonia diomedea are closely related to Aplysia punctata belonging to the systematic group of ophistobranchia. Here we look for serotonin immunoreactivity in the rhinophore of Aplysia punctata. In addition, neuroanatomical tracing and histology are used to analyse the structure of the rhinophore.
Amino acids were shown to be potent olfactory stimuli for aquatic animals [28–31] and elicit feeding responses in Pleurobranchaea californica . Murphy and Hadfield  studied the innervation of the rhinophores and the oral tentacles of Phestilla sibogae and used electrophysiological techniques to demonstrate that only the rhinophores were highly selective to free amino acids. Therefore we use optical imaging technique and amino acids as stimuli, to investigate chemoreceptive processing in the rhinophore. The present study is aimed to contribute to our understanding of the olfactory sensory pathway in marine snails and the chemosensory capabilities of these animals.
Neuroanatomy of the rhinophore
The number of glomeruli was estimated in a complete series of sections of the rhinophore labelled with 5-HT antibody. The total number of glomeruli counted in one rhinophore was 36 in one rhinophore, and the mean diameter of individual glomeruli averaged 49 μm +/- 27 μm with a range from 25 μm to 135 μm.
Previous investigations on Aplysia californica have shown that the groove houses various types of sensory cells . Emery and Audesirk  suggested that intraepithelial cells with 30 μM long cilia produce a steady water flow around the epithelial cells of the rhinophore to facilitate olfaction. Anterograde labelling experiments in a terrestrial snail (Achatina fulica) by Chase and Tollozcko  have shown that sensory neurons project to the glomeruli and directly to the rhinophore ganglion or to further centres in the cerebral ganglion. Future experiments are needed to find out if similar projection patterns of sensory neurons are present in Aplysia.
Labelling of cell nuclei with propidium iodide and histological sections showed the high amount of cell nuclei in the sensory epithelium (Figs 1F, G, 2A, H, I). The layer of sensory cell nuclei is clearly separated from the more basal nuclei (Fig 2H). Glomeruli were located underneath this epithelium (Figs 2H, I).
Propidium Iodide and Mallory's stain revealed cell nuclei of variable sizes surrounding the glomeruli. Both methods revealed very few nuclei inside the glomeruli similar to the conditions in vertebrates and in insects (Figs. 2H, I). Propidium Iodide has very high affinity to nucleic acids, and since we used agarose sections with excellent penetration properties we are convinced that all nuclei were labelled. In contrast to the glomeruli, cell nuclei were present inside the rhinophore ganglion (Fig. 2G). Cell nuclei can be from both neuronal and glial cell bodies.
The anatomy of the rhinophores with distributed glomeruli around the groove leaves different possibilities open for central projections of olfactory receptor neurons (ORNs). The general view of a uniglomerular projection pattern, which seems to occur in most insects [39, 40] and vertebrates [41, 42], would be complicated with the present arrangement of glomeruli. Possibly, ORNs of the same type are situated beneath one glomerulus and are not uniformly distributed over the sensory epithelium, or, in the other case, axonal projections of individual ORNs to their target glomeruli would be very long and across the rhinophore. Recent studies in Xenopus laevis described an innervation of more than one glomerulus by individual ORNs . Multiglomerular projection patterns also appear in crustaceans . In Aplysia, future studies on the projection pattern of ORNs combined with functional imaging studies of the glomeruli will provide further insight in the functional role of glomeruli in molluscs.
Calcium imaging of odour evoked responses within the rhinophore ganglion
We chose different amino acids, as they were used in previous experiments in gastropod molluscs [32, 33]. To avoid direct excitation of neurons within the rhinophore by the stimuli, we did not use glutamic and aspartic acid, which induced highest responses in the nudibranch Phestilla sibogae . In more than 10 experiments we found no Ca2+ – response within the rhinophore ganglion induced by the application of methionin at different concentration (200 μm – 20 mM).
Clear Ca2+-responses within the rhinophore ganglion were found during stimulation with alanine (ALA). Figure 3B shows three responses to ALA from three different animals. In all experiments 2 mM ALA was applied. We found a decrease of Ca2+-levels as well as an increase (Fig 3B upper trace). Application of different amino acids (2 mM each) during one experiment revealed differential responses of intracellular Ca2+-levels in distinct regions (Fig 3C). The traces in Fig 3C show Ca2+-measurements in two different regions of interest. Arginine (ARG) and glutamine (GLN) induced a response in one region, whereas the other region showed no response, but both regions responded with a change in Ca2+-level to the stimulation with glycine (GLY) and valine (VAL). Both regions showed a decrease in Ca2+-levels to all stimuli (Fig. 3C) indicating an inhibition or reduction of cellular activity by these stimuli. Stimulation with 2 mM phenylalanine (PHE) induced no detectable responses.
In the course of a single experiment, odour induced responses to amino acids recorded from different regions remained similar. We applied ALA in concentration from 2 μm to 20 mM. At low concentration (<2 mM) it was difficult to decide whether an observed Ca2+-response was stimulus dependent. At a concentration of 2 mM ALA, clear responses could be observed in three regions (Fig 4C VIII-X). Regions VIII and IX showed a decrease of the Ca2+-levels, whereas in region X the Ca2+-level increased.
In response to 20 mM ALA all of the selected regions showed a change in intracellular Ca2+-levels. It was either a decrease or an increase of the Ca2+-levels, or even a combination of both as shown in trace II. Remarkably, responses from neighbouring regions (II and III; IX and X) showed opposing Ca2+-responses indicating a possible inhibitory coupling. The spatial response patterns were complex. Stimulation with 20 mM ALA induced an increase in Ca2+-levels in four regions (Fig. 3A-I,-V,-VI,-X), whereas in five other regions we found a decrease in Ca2+-levels (Fig. 3A-III,-IV,-VII,-VIII,-IX), and in region II a decrease was followed by an increase in Ca2+-levels.
In all of our experiments, the highest Ca2+-responses were induced by ALA. Since the rhinophore is cut during the preparation, we cannot exclude partial injury of the rhinophore ganglia. However, the calcium imaging experiments demonstrate that parts of the rhinophore ganglion respond differentially to stimulation of the sensory epithelium with amino acids indicating that olfactory stimuli are relayed and processed in the rhinophore ganglion. In a previous investigation we tested sponge alkaloids and revealed clear responses to sceptrin at 200 μM concentration . The term olfaction is used in terrestrial animals for airborne chemicals, but also in aquatic animals for water borne chemicals detected by primary receptor neurons in the nose (e.g. fish, amphibians) or on the antennae (crustaceans) . In vertebrates it is referred to as long distance reception in contrast to close range chemoreception via taste receptors (secondary receptor cells). In Phestilla sibogae different densities of subepithelial sensory cells and intraepithelial sensory cells were found in the oral tentacle and the rhinophores . These morphological data together with the electrophysiological evidence for greater sensitivity of the rhinophores  led Boudko and colleagues  to the conclusion, that rhinophores serve for long-distance chemoreception or olfaction. To our knowledge, a clear separation based on receptor cell morphology has not been done for Aplysia; therefore we prefer to use the term "olfaction" because of the apparent similarities regarding the organization of the central pathway in glomeruli.
In Limax, processing of olfactory information was mainly investigated at the level of the procerebrum [47–49], and complex odour induced oscillations were described. In Aplysia, using calcium imaging techniques we did not find any indications for odour induced oscillations at the level of the rhinophore ganglion. However, the complexity of changes in intracellular Ca2+-levels indicates that processing of odour information takes place within the rhinophore ganglion.
The spatial distribution of odour induced activity recorded in this study indicates that the activity in the rhinophore ganglion depends on the chemical nature and intensity of the stimulus.
Various studies in insects as well as vertebrates suggest that olfactory glomeruli represent functional units for odour processing, and olfactory information is represented in a spatial map of differentially activated glomeruli (e.g.:[50, 51]). It will be interesting to determine if this is also the case in Aplysia and if glomeruli represent functional units for odour processing. Glomeruli diameters ranged between 25 μm and 135 μm indicating different numbers of neurons converging in one glomerulus. In insects, macroglomeruli were found to play an important role in pheromone communication (e.g.: [52, 53]). As the rhinophore of Aplysia plays an important role in pheromone detection , it would be interesting to investigate the large glomeruli and their potential function in pheromone processing. Measuring the responses of sensory neurons in the epithelium may also help to identify olfactory sensory neurons. Many marine organisms produce secondary metabolites for defence, deterrence and as pheromones. Sea slugs as well as many other marine animals depend on chemosensory information from their aquatic environment, as the optical sense plays a minor role in shallow muddy waters or the deep sea and acoustic/mechano-sensory senses give only limited information about for example food quality. The chemical sense probably is the primary sense in many marine organisms, and Aplysia represents a promising model system for future investigations of the chemical ecology of sea slugs.
The glomeruli and the rhinophore ganglion represent different processing stages for sensory information. We found 36 glomeruli in the rhinophore and retrograde labelling with DiA revealed the connection between glomeruli and rhinophore ganglion. The glomeruli are situated close to the epithelials layers towards the lumen of the groove and appear to be surrounded by a thin glia-like sheath. Serotonin-immunoreactivity was found extensively within the rhinophore, but was not detected in any peripheral cell body. Therefore these serotonergic fibres appear to be efferent projections from central ganglia. Amino acids were used as potentially important olfactory stimuli for aquatic animals, and optical recordings show that amino acids induce sensory responses in the rhinophore. The complexity of changes in intracellular Ca2+-levels led us suggest, that processing of odour information takes place within the rhinophore ganglion. Our neuroanatomical and functional studies of the rhinophore open up a new avenue to analyze the olfactory system in Aplysia, leading towards understanding neuronal processing of chemical cues in the marine environment.
Tissue preparation, immunocytochemistry, and fluorescent tracers
Specimens of Aplysia punctata were collected from shallow waters around Helgoland. Animals were cooled in ice, fixed in 4% formaldehyde in Artificial Sea Water (ASW; pH 7.5; in mM: 460 NaCl, 104 KCl, 55 MgCl, 11 CaCl2, and 15 Na -HEPES (N-(2-hydroxyethyl) piperazine-N-2-ethansulfonic acid Na-salt). Before further treatments rhinophores were washed three times in 0.1 M phosphate buffered saline (PBS; pH 7.2). For labelling with fluophore-conjugated phalloidin, immunocytochemistry, tracing with lipophilic markers and nuclear staining, the rhinophores were embedded in 5% low-melting point agarose (Agarose II, Amresco, Solon, OH, No. 210–815) and sectioned in a frontal or sagittal plane at 150 μm thickness with a vibrating microtome (Leica VT 1000S, Wetzlar, Germany). Free-floating agarose sections were preincubated in PBS with 0.2% Triton X-100 and 2% normal goat serum (ICN, Biomedicals, Orsay, France, Cat. No.191356) for one hour at room temperature. Different combinations of double stainings were performed. To label serotonergic neurons, sections were incubated with a primary antibody against 5-HT, raised in rabbit (1:4000, DiaSorin, Stillwater, MN, Cat. No. 20080, Lot No. 051007) in PBS with 0.2% Triton X-100 and 2% NGS overnight at room temperature. This antibody was used in previous studies in gastropod molluscs [26, 27]. After five rinses in PBS, sections were incubated in Alexa Fluor 488 conjugated goat anti-rabbit secondary antibody (1:250, Molecular Probes, Eugene, OR, Cat. No. A -11008). To label filamentous (f)-actin in muscles and neurons, sections were incubated in 0.2 units of Alexa Fluor 488 or 568 phalloidin (Molecular probes, A-12379 and A-12380) in PBS overnight at 4°C. To stain cell nuclei, sections were incubated for 15 min in 25 μg/ml propidium iodide (Molecular probes, P-1304) in PBS with 0.2% Triton X-100 at room temperature. Sections were finally washed at least five times with PBS, transferred into 60% glycerol/PBS for 30 min, and mounted on slides in 80% glycerol in PBS.
Staining with lipophilic tracers
The fluorescent lipophilic dye 4-(4-(dihexadecylamino)styryl)-N-methylpyridinium iodide (DiA; Molecular Probes, D -3883) was used as retrograde tracer. Crystals of DiA were transferred into the rhinophore ganglion with a fine minuten pin. Following dye application the rhinophores were fixed in 4% formaldehyde in PBS and incubated for 7 days at 4°C. Embedding, sectioning and double labelling with propidium iodide were performed as described above. Finally, sections were rinsed in PBS and mounted in PBS on microscopic slides.
Histology, Mallory's stain and microscopy
Rhinophores were fixed in Bouin's fixative solution for 2 days, washed with ethanol, embedded in Spurr's resin and sectioned in a frontal plane (6 μm). After normal histological procedures, the plastic sections were stained after the method from Mallory (for details ) on a hotplate. The sections were washed with distilled water, dried on the hotplate and mounted in Entellan (Merck,. Darmstadt, Germany). Images were taken with a digital Camera (Spotinsight Color, Vistron Systems, Puchheim, Germany) mounted on a microscope (Zeiss Axiophot, Carl Zeiss GmbH, Jena, Germany). Image processing was performed with CorelDRAW Graphics Suite (Corel Corporation, Ottawa, Ontario, Canada).
Fluorescent tracers and antibodies were visualized using a laser-scanning confocal microscope (Leica TCS SP). Glomeruli counts per slice were corrected for double-counting in adjacent slices using the method after Weibel . Image processing was performed with the following software: Zeiss Image Browser (Zeiss GmbH, Jena, Germany), Corel Photopaint and CorelDRAW Graphics Suite (Corel Corporation, Ottawa, Ontario, Canada), and Adobe Photoshop (Adobe, San Jose, USA).
Fluorimetric measurements of intracellular Ca2+ levels
All physiological experiments were performed at the marine station Helgoland. The rhinophores were dissected as described above and cut longitudinally using a razor blaze. The half containing the ganglion was incubated for 60 min at 4°C with ASW containing 5 μM Fura II acetoxymethylester (AM). After removal of the incubation buffer the rhinophores were washed for 10 min. Changes in fluorescence were monitored with an imaging system (Visitron, Puchheim) and a CCD camera mounted on an inverted microscope (Zeiss Axiovert 100) equipped with a UV objective (Zeiss NeoFluar 20X). Different regions within the rhinophore ganglion were measured using the "region" function of the software (Metafluor, Meta Imaging Series, Universal Imaging Corporation). Changes in fluorescence were obtained by ratiometric measurements with excitation at 340 nm and 380 nm excitation. Values were presented as relative changes in ratios representing alterations in intracellular Ca2+-levels. Fluorescence images were acquired with an interval of 5 s and an exposure time of 50 ms per image.
For odour stimulation the recording chamber (volume 3 ml) was mounted on the microscope stage, and the bath flow was adjusted to 4 ml/min with a peristaltic pump. The chamber volume was exchanged in less than one minute. Amino acids, which induced the highest response in Pleurobranchea californica  were chosen: Alanine, Arginine, Glutamine, Glycine, Phenylalanine, Methionine and Valine. Amino acids (Sigma-Aldrich, Munich, Germany) were applied for one minute at various concentrations with the peristaltic pump system. In control experiments, the rhinophore ganglion was removed and treated similar as the rhinophore obtaining no response to amino acids. Each amino acid (1 M stock each) was dissolved in ASW and final concentrations ranged from 2 μM to 20 mM. Stimulus solutions were prepared immediately before use by dissolving the respective stock solution in ASW. After application the recording chamber was washed with ASW for at least 10 min to remove all amino acids possibly attached to the rhinophore. In most cases, 50 regions were measured simultaneously. As a control for the viability of the preparations the last stimulus at the end of an experiment was a high K+ buffer stimulation (400 mM NaCl was replaced by 400 mM KCl), which always elicited a strong response. Calcium-imaging experiments were performed with 25 (K+)-responsive rhinophores.
We thank the diving group of Udo Schilling and Carsten Wanke (Helgoland) for collecting animals and Dr. Christoph Kleineidam (Würzburg) for critical discussion of the experimental results.
- Luporini P, Vallesi A, Miceli C, Bradshaw RA: Chemical Signaling in Ciliates. Journal of Eukaryotic Microbiology. 1995, 42: 208-212.View ArticlePubMedGoogle Scholar
- Kodama T, Hisatomi T, Kanemura T, Mokubo K, Tsuboi M: Molecular cloning and DNA analysis of a gene encoding alpha mating pheromone from the yeast Saccharomyces naganishii. Yeast. 2003, 20: 109-115. 10.1002/yea.939.View ArticlePubMedGoogle Scholar
- Monsma SA, Wolfner MF: Structure and Expression of A Drosophila Male Accessory-Gland Gene Whose Product Resembles A Peptide Pheromone Precursor. Genes & Development. 1988, 2: 1063-1073.View ArticleGoogle Scholar
- Painter SD, Clough B, Garden RW, Sweedler JV, Nagle GT: Characterization of Aplysia attractin, the first water-borne peptide pheromone in invertebrates. Biological Bulletin. 1998, 194: 120-131.View ArticlePubMedGoogle Scholar
- Susswein AJ, Nagle GT: Peptide and protein pheromones in molluscs. Peptides. 2004, 25: 1523-1530. 10.1016/j.peptides.2003.11.027.View ArticlePubMedGoogle Scholar
- Li WM, Scott AP, Siefkes MJ, Yan HG, Liu Q, Yun SS, Gage DA: Bite acid secreted by mate sea lamprey that acts as a sex pheromone. Science. 2002, 296: 138-141. 10.1126/science.1067797.View ArticlePubMedGoogle Scholar
- Novotny MV: Pheromones, binding proteins and receptor responses in rodents. Biochemical Society Transactions. 2003, 31: 117-122.View ArticlePubMedGoogle Scholar
- Savic I, Berglund H, Gulyas B, Roland P: Smelling of odorous sex hormone-like compounds causes sex-differentiated hypothalamic activations in humans. Neuron. 2001, 31: 661-668. 10.1016/S0896-6273(01)00390-7.View ArticlePubMedGoogle Scholar
- Castellucci VF, Carew TJ, Kandel ER: Cellular Analysis of Long-Term Habituation of Gill-Withdrawal Reflex of Aplysia-Californica. Science. 1978, 202: 1306-1308.View ArticlePubMedGoogle Scholar
- Kandel ER: Neuroscience - The molecular biology of memory storage: A dialogue between genes and synapses. Science. 2001, 294: 1030-1038. 10.1126/science.1067020.View ArticlePubMedGoogle Scholar
- Kupfermann I, Carew TJ: Behavior Patterns of Aplysia-Californica in Its Natural-Environment. Behavioral Biology. 1974, 12: 317-337. 10.1016/S0091-6773(74)91503-X.View ArticlePubMedGoogle Scholar
- Audesirk TE, Audesirk GJ: Chemoreception in Aplysia-Californica .2. Electrophysiological Evidence for Detection of Odor of Conspecifics. Comparative Biochemistry and Physiology A-Physiology. 1977, 56: 267-270. 10.1016/0300-9629(77)90234-1.View ArticleGoogle Scholar
- Emery DG, Audesirk TE: Sensory cells in Aplysia. J Neurobiol. 1978, 9: 173-179. 10.1002/neu.480090207.View ArticlePubMedGoogle Scholar
- Jahan-Parvar B: Behavioral and Electrophysiological Studies on Chemoreception in Aplysia. American Zoologist. 1972, 12: 525-&.View ArticleGoogle Scholar
- Audesirk TE: Chemoreception in Aplysia californica. I. Behavioral localization of distance chemoreceptors used in food-finding. Behav Biol. 1975, 15: 45-55. 10.1016/S0091-6773(75)92066-0.View ArticlePubMedGoogle Scholar
- Teyke T, Susswein AJ: Pheromones linked to sexual behaviors excite the appetitive phase of feeding behavior of Aplysia fasciata II. Excitation of C-PR, a neuron involved in the generation of appetitive behaviors. Journal of Comparative Physiology A-Sensory Neural and Behavioral Physiology. 1998, 182: 785-791. 10.1007/s003590050223.View ArticleGoogle Scholar
- Levy M, Blumberg S, Susswein AJ: The rhinophores sense pheromones regulating multiple behaviors in Aplysia fasciata. Neuroscience Letters. 1997, 225: 113-116. 10.1016/S0304-3940(97)00200-0.View ArticlePubMedGoogle Scholar
- Cummins SF, Nichols AE, Rajarathnam K, Nagle GT: A conserved heptapeptide sequence in the waterborne attractin pheromone stimulates mate attraction in Aplysia. Peptides. 2004, 25: 185-189. 10.1016/j.peptides.2003.12.018.View ArticlePubMedGoogle Scholar
- Painter SD, Clough B, Black S, Nagle GT: Behavioral characterization of attractin, a water-borne peptide pheromone in the genus Aplysia. Biological Bulletin. 2003, 205: 16-25.View ArticlePubMedGoogle Scholar
- Bickmeyer U, Drechsler C, Kock M, Assmann M: Brominated pyrrole alkaloids from marine Agelas sponges reduce depolarization-induced cellular calcium elevation. Toxicon. 2004, 44: 45-51. 10.1016/j.toxicon.2004.04.001.View ArticlePubMedGoogle Scholar
- Chase R, Tolloczko B: Tracing Neural Pathways in Snail Olfaction - from the Tip of the Tentacles to the Brain and Beyond. Microscopy Research and Technique. 1993, 24: 214-230. 10.1002/jemt.1070240303.View ArticlePubMedGoogle Scholar
- Chase R: Photic Sensitivity of the Rhinophore in Aplysia. Canadian Journal of Zoology-Revue Canadienne de Zoologie. 1979, 57: 698-701.View ArticleGoogle Scholar
- Jacklet JW: Electrophysiological organization of the eye of Aplysia. J Gen Physiol. 1969, 53: 21-42. 10.1085/jgp.53.1.21.PubMed CentralView ArticlePubMedGoogle Scholar
- Jacklet JW: Light Sensitivity of the Rhinophores and Eyes of Aplysia. Journal of Comparative Physiology. 1980, 136: 257-262. 10.1007/BF00657541.View ArticleGoogle Scholar
- Croll RP, Boudko DY, Hadfield MG: Histochemical survey of transmitters in the central ganglia of the gastropod mollusc Phestilla sibogae. Cell and Tissue Research. 2001, 305: 417-432. 10.1007/s004410100394.View ArticlePubMedGoogle Scholar
- Croll RP, Boudko DY, Pires A, Hadfield MG: Transmitter contents of cells and fibers in the cephalic sensory organs of the gastropod mollusc Phestilla sibogae. Cell and Tissue Research. 2003, 314: 437-448. 10.1007/s00441-003-0778-1.View ArticlePubMedGoogle Scholar
- Moroz LL, Sudlow LC, Jing J, Gillette R: Serotonin-immunoreactivity in peripheral tissues of the opisthobranch molluscs Pleurobranchaea californica and Tritonia diomedea. Journal of Comparative Neurology. 1997, 382: 176-188. 10.1002/(SICI)1096-9861(19970602)382:2<176::AID-CNE3>3.0.CO;2-0.View ArticlePubMedGoogle Scholar
- Caprio J, Byrd RPJ: Electrophysiological evidence for acidic, basic, and neutral amino acid olfactory receptor sites in the catfish. J Gen Physiol. 1984, 84: 403-422. 10.1085/jgp.84.3.403.View ArticlePubMedGoogle Scholar
- Chiken S, Kuwasawa K, Kurokawa M, Ohsuga K: Amino acid-induced reflexes and their neural pathways in an opisthobranch mollusc Pleurobranchaea japonica. Zoological Science. 2001, 18: 465-473. 10.2108/zsj.18.465.View ArticleGoogle Scholar
- Czesnik D, Rossler W, Kirchner F, Gennerich A, Schild D: Neuronal representation of odourants in the olfactory bulb of Xenopus laevis tadpoles. European Journal of Neuroscience. 2003, 17: 113-118. 10.1046/j.1460-9568.2003.02448.x.View ArticlePubMedGoogle Scholar
- Manzini I, Schild D: Classes and narrowing selectivity of olfactory receptor neurons of Xenopus laevis tadpoles. Journal of General Physiology. 2004, 123: 99-107. 10.1085/jgp.200308970.PubMed CentralView ArticlePubMedGoogle Scholar
- Bicker G, Davis WJ, Matera EM, Kovac MP, Stormogipson DJ: Chemoreception and Mechanoreception in the Gastropod Mollusk Pleurobranchaea-Californica .1. Extracellular Analysis of Afferent Pathways. Journal of Comparative Physiology. 1982, 149: 221-234. 10.1007/BF00619216.View ArticleGoogle Scholar
- Murphy BF, Hadfield MG: Chemoreception in the nudibranch gastropod Phestilla sibogae. Comparative Biochemistry and Physiology Part A: Physiology. 1997, 118: 727-735. 10.1016/S0300-9629(97)00014-5.View ArticleGoogle Scholar
- Klussmann-Kolb A: Phylogeny of the Aplysiidae (Gastropoda, Opisthobranchia) with new aspects of the evolution of seahares. Zoologica Scripta. 2004, 33: 439-462. 10.1111/j.0300-3256.2004.00158.x.View ArticleGoogle Scholar
- Croll RP: Catecholamine-containing cells in the central nervous system and periphery of Aplysia californica. J Comp Neurol. 2001, 441: 91-105. 10.1002/cne.1399.View ArticlePubMedGoogle Scholar
- Kloppenburg P, Ferns D, Mercer AR: Serotonin enhances central olfactory neuron responses to female sex pheromone in the male sphinx moth Manduca sexta. Journal of Neuroscience. 1999, 19: 8172-8181.PubMedGoogle Scholar
- Sun XJ, Tolbert LP, Hildebrand JG: Ramification Pattern and Ultrastructural Characteristics of the Serotonin-Immunoreactive Neuron in the Antennal Lobe of the Moth Manduca-Sexta - A Laser-Scanning Confocal and Electron-Microscopic Study. Journal of Comparative Neurology. 1993, 338: 5-16. 10.1002/cne.903380103.View ArticlePubMedGoogle Scholar
- Rossler W, Kuduz J, Schurmann FW, Schild D: Aggregation of F-actin in olfactory glomeruli: a common feature of glomeruli across phyla. Chemical Senses. 2002, 27: 803-810. 10.1093/chemse/27.9.803.View ArticlePubMedGoogle Scholar
- Boeckh J, Tolbert LP: Synaptic Organization and Development of the Antennal Lobe in Insects. Microscopy Research and Technique. 1993, 24: 260-280. 10.1002/jemt.1070240305.View ArticlePubMedGoogle Scholar
- Hildebrand JG, Shepherd GM: Mechanisms of olfactory discrimination: converging evidence for common principles across phyla. Annu Rev Neurosci. 1997, 20: 595-631. 10.1146/annurev.neuro.20.1.595.View ArticlePubMedGoogle Scholar
- Mombaerts P, Wang F, Dulac C, Chao SK, Nemes A, Mendelsohn M, Edmondson J, Axel R: Visualizing an olfactory sensory map. Cell. 1996, 87: 675-686. 10.1016/S0092-8674(00)81387-2.View ArticlePubMedGoogle Scholar
- Mombaerts P: Targeting olfaction. Faseb Journal. 2003, 17: A1377-A1377. 10.1096/fj.03-0002hyp.View ArticleGoogle Scholar
- Nezlin LP, Schild D: Individual olfactory sensory neurons project into more than one glomerulus in Xenopus laevis tadpole olfactory bulb. Journal of Comparative Neurology. 2005, 481: 233-239. 10.1002/cne.20390.View ArticlePubMedGoogle Scholar
- Schmidt M, Ache BW: Antennular Projections to the Midbrain of the Spiny Lobster .2. Sensory Innervation of the Olfactory Lobe. Journal of Comparative Neurology. 1992, 318: 291-303. 10.1002/cne.903180306.View ArticlePubMedGoogle Scholar
- Finger TE, W.L. S, Restrepo D: The Neurobiology of Taste and Smell. 2000, Wiley-Liss, 2Google Scholar
- Boudko DY, Switzer-Dunlap M, Hadfield MG: Cellular and subcellular structure of anterior sensory pathways in Phestilla sibogae (Gastropoda, Nudibranchia). Journal of Comparative Neurology. 1999, 403: 39-52. 10.1002/(SICI)1096-9861(19990105)403:1<39::AID-CNE4>3.0.CO;2-B.View ArticlePubMedGoogle Scholar
- Delaney KR, Gelperin A, Fee MS, Flores JA, Gervais R, Tank DW, Kleinfeld D: Waves and stimulus-modulated dynamics in an oscillating olfactory network. Proc Natl Acad Sci U S A. 1994, 91: 669-673. 10.1073/pnas.91.2.669.PubMed CentralView ArticlePubMedGoogle Scholar
- Gelperin A, Tank DW: Odor-Modulated Collective Network Oscillations of Olfactory Interneurons in A Terrestrial Mollusk. Nature. 1990, 345: 437-440. 10.1038/345437a0.View ArticlePubMedGoogle Scholar
- Gelperin A: Oscillatory dynamics and information processing in olfactory systems. J Exp Biol. 1999, 202 (Pt 14): 1855-1864.Google Scholar
- Friedrich RW, Korsching SI: Chemotopic, combinatorial, and noncombinatorial odorant representations in the olfactory bulb revealed using a voltage-sensitive axon tracer. J Neurosci. 1998, 18: 9977-9988.PubMedGoogle Scholar
- Jorges U, Jummel G: Correct macromodelling of the common mode and power supply rejections of operational amplifiers. International Journal of Numerical Modelling-Electronic Networks Devices and Fields. 1996, 9: 397-404. 10.1002/(SICI)1099-1204(199611)9:6<397::AID-JNM243>3.0.CO;2-1.View ArticleGoogle Scholar
- Hansson BS, Anton S: Function and morphology of the antennal lobe: new developments. Annu Rev Entomol. 2000, 45: 203-231. 10.1146/annurev.ento.45.1.203.View ArticlePubMedGoogle Scholar
- Kleineidam CJ, Obermayer M, Halbich W, Rossler W: A macroglomerulus in the antennal lobe of leaf-cutting ant workers and its possible functional significance. Chemical Senses. 2005, 30: 383-392. 10.1093/chemse/bji033.View ArticlePubMedGoogle Scholar
- Mallory FB: A contribution to staining methods: I. A differential stain for connective-tissue fibrillae and reticulum. II. Chloride of iron haematoxylin for nuclei and fibrin. III. Phosphotungstic acid haematoxylin for neuroglia fibres. Journal of Experimental Medicine. 1900, 15-20. 10.1084/jem.5.1.15.Google Scholar
- Weibel ER: Stereological Methods. Vol. 2: Practical Methods for Biological Morphometry. Academic Press, London. 1979Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.