Skip to main content
Log in

Ultrastructure of the lateral-line sense organs of the ratfish, Chimaera monstrosa

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Summary

The ultrastructure of the lateral-line neuromasts in the ratfish, Chimaera monstrosa is described. The neuromasts rest at the bottom of open grooves and consist of sensory, supporting, basal and mantle cells. Each sensory cell is equipped with sensory hairs consisting of a single kinocilium and several stereocilia. There are several types of sensory hair arrangement, and cells with a particular arrangement form patches within the neuromast. There are two types of afferent synapse. The most common afferent synapse has a presynaptic body and is typically associated with an extensive system of anastomosing tubules on the presynaptic side. When the tubules are absent, vesicles surround the presynaptic body. These synapses are often associated into synaptic fields, containing up to 35 synaptic sites. The second type of afferent synapse does not have a presynaptic body and is not associated with the tubular system. The afferent synapses of the second type do not form synaptic fields and are uncommon. The efferent synapses are either associated with a postsynaptic sac or more commonly with a strongly osmiophilic postsynaptic membrane. The accessory cells are similar to those in the acoustico-lateralis organs of other aquatic vertebrates. A possibility of movement of the presynaptic bodies and of involvement of the tubular system in the turnover of the transmitter is discussed. A comparison of the hair tuft types in the neuromasts of Ch. monstrosa with those in the labyrinth of the goldfish and of the frog is attempted.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bodian DA (1936) New method for staining nerve fibers and nerve endings in mounted paraffine sections. Anat Rec 65:65–89

    Google Scholar 

  • Dijkgraaf S (1963) The functioning and significance of the lateral line organs. Biol Rev 38:51–105

    Google Scholar 

  • Ewart JC (1893) The lateral line sense organs of Elasmobranchs. I. The sensory canals of Laemargus. Trans Roy Soc Edinb 37:59–86

    Google Scholar 

  • Ewart JC, Mitchell JC (1893) II. The sensory canals of the common skate (Raia batis). Trans Roy Soc Edinb 37:787–806

    Google Scholar 

  • Flock Å (1964) Structure of the macula utriculi with special reference to directional interplay of sensory response as revealed by morphological polarisation. J Cell Biol 22:413–431

    Google Scholar 

  • Flock Å (1965) Electronmicroscope and electrophysiological studies on the lateral line canal organ. Acta Oto-laryng Suppl 199:90

    Google Scholar 

  • Flock Å, Jørgensen J Mørup, Russell I (1973) The physiology of individual hair cells and their synapses. In: Møller A (ed) Basic Mechanisms in Hearing. Academic Press, New York, pp 273–306

    Google Scholar 

  • Flock Å, Jørgensen J Mørup (1974) The ultrastructure of lateral line organs in the juvenile salamander Ambystoma mexicanum. Cell Tissue Res 152:283–292

    Google Scholar 

  • Garman S (1888) On the lateral system of the Selachia and Holocephali. Bull Mus Comp Zool Cambr 17/2:57–117

    Google Scholar 

  • Gray EG (1976a) Problems of understanding the substructure of synapses. Prog Brain Res 45:207–234

    Google Scholar 

  • Gray EG (1976b) Microtubules in synapses of the retina. J Neurocytol 5:361–370

    Google Scholar 

  • Gray EG (1977) Presynaptic microtubules, agranular reticulum and synaptic vesicles. In: Cottrell GA, Usherwood PNR (eds) Synapses. Blackie, Glasgow London, pp 6–18

    Google Scholar 

  • Hama K (1965) Some observations on the fine structure of the lateral line organ of the Japanese sea eel, Lancozymba nystromi. J Cell Biol 24:193–210

    Google Scholar 

  • Hama K (1978) A study of the fine structure of the pit organ of the common Japanese sea eel, Conger myriaster. Cell Tissue Res 189:375–388

    Google Scholar 

  • Hama K., Saito K (1977) Fine structure of the afferent synapse of the hair cells in the saccular macula of the goldfish, with special reference to the anastomosing tubules. J Neurocytol 6:361–373

    Google Scholar 

  • Hama K, Yamada Y (1977) Fine structure of the ordinary lateral line organ. II. The lateral line canal of spotted shark, Mustelus manzo. Cell Tissue Res 176:23–36

    Google Scholar 

  • Hillman DE (1976) Vestibular and lateral line system. 14. Morphology of peripheral and central vestibular system. In: Llinás R, Precht W (eds) Frog neurobiology. Springer, Berlin Heidelberg New York, pp 453–475

    Google Scholar 

  • Hirokawa N (1977) Disappearance of afferent and efferent nerve terminals in the inner ear of the chick embryo after chronic treatment with beta-bugarotoxin. J Cell Biol 73:27–46

    Google Scholar 

  • Jande SS (1966) Fine structure of lateral line organs of frog tadpoles. J Ultrastruct Res 15:496–509

    Google Scholar 

  • Johnson SE (1917) Structure and development of the sense organs of the lateral line canal system of selachians (Mustelus canis and Squalus acanthias). J Comp Neurol 28/1:1–74

    Google Scholar 

  • Jørgensen J Mørup, Flock Å (1973) The ultrastructure of lateral line sense organs in the adult salamander Ambystoma mexicanum. J Neurocytol 2:133–142

    Google Scholar 

  • Jørgensen J Mørup, Flock Å (1976) Non-innervated sense organs of the lateral line: development in the regenerating tail of salamander, Ambystoma mexicanum. J Neurocytol 5:33–41

    Google Scholar 

  • Kalt MR, Tandler B (1971) A study of fixation of early amphibian embryos for electron microscopy. J Ultrastr Res 36:633–645

    Google Scholar 

  • Loewenstein O, Osborne MP, Wersäll J (1964) Structure and innervation of the labyrinth in the thornback ray (Raia clavata). Proc Roy Soc Lond B 160:1–12

    Google Scholar 

  • Luft JH (1961) Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol 9:409–414

    Article  CAS  PubMed  Google Scholar 

  • McArdle CB, Dowling JE, Masland RH (1977) Development of outer segments and synapses in the rabbit retina. J Comp Neurol 175:253–274

    Google Scholar 

  • Palmgren A (1955) Staining nerve fibers after sublimate-acetic and after Bouin's fluid fixation. Stain Technol 30:31–36

    Google Scholar 

  • Platt Ch (1977) Hair cell orientation in goldfish otolith organs. J Comp Neurol 172:283–298

    CAS  PubMed  Google Scholar 

  • Pujol R, Abonnenc M (1977) Receptor maturation and synaptogenesis in golden hamster cochlea. Arch Oto-Rhino-Laryng 217:1–12

    Google Scholar 

  • Pumphrey RJ (1950) Hearing. Soc Exp Biol Symposium 4:3–18

    Google Scholar 

  • Reese AM (1910) The lateral line system of Chimaera colliei. J Exp Zool 9:349–370

    Google Scholar 

  • Roberts BL, Ryan RP (1971) The fine structure of the lateral line sense organs of dogfish. Proc Roy Soc Lond B 179:157–169

    Google Scholar 

  • Ruud G (1917) Sinneslinien und freie Nervenhügel bei Chimaera monstrosa. Zool Jahrbücher Abt für Anat und Ontog der Tiere 40:421–440

    Google Scholar 

  • Ruud G (1920) Über Hautsinnesorgane bei Spinax niger Bon. II. Die embryologische Entwicklung. Zool Jahrbücher Abt für Anatomie 41:459–546

    Google Scholar 

  • Schwartz E (1974) Lateral-line mechanoreceptors in fishes and amphibians. In: Autrum H (ed) Handbook of sensory physiology Vol 13/3. Springer, Berlin Heidelberg New York, pp 257–270

    Google Scholar 

  • Solger B (1880) Neue Untersuchungen zur Anatomie der Seitenlinie der Fische. I. Die Seitenorgane von Chimaera. Arch Mikr Anat 17:95–113

    Google Scholar 

  • Tester A, Kendall JI (1967) Innervation of free and canal neuromast in the sharks Carcharhinus menissorah and Sphyrna lewini. In: Cahn Ph (ed) Lateral line detectors. Indiana University Press, Bloomington, pp 53–69

    Google Scholar 

  • Tester A, Kendall JI (1969) Morphology of the lateralis canal system in the shark genus Carcharhinus. Pacific Science 23:1–16

    Google Scholar 

  • Trujillo-Cenóz O (1961) Electron microscope observations on chemo- and mechanoreceptor cells of some fishes. Z Zellforsch 54:654–676

    Google Scholar 

  • Vollrath L (1973) Synaptic ribbons of a mammalian pinal gland. Circadian changes. Z Zellforsch 145:171–183

    Google Scholar 

  • Vollrath L, Huss H (1973) The synaptic ribbons of the guinea-pig pineal organ under normal and experimental conditions. Z Zellforsch 139:417–429

    Google Scholar 

  • Walker TJ (1967) History, histological methods and details of the lateral line in the walleye surf perch. In: Cahn Ph (ed) Lateral line detectors. Indiana University Press, Bloomington, pp 13–25

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

von Lubitz, D.K.J.E. Ultrastructure of the lateral-line sense organs of the ratfish, Chimaera monstrosa . Cell Tissue Res. 215, 651–665 (1981). https://doi.org/10.1007/BF00233539

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00233539

Key words

Navigation