Skip to main content
Log in

Fine structure of the cerebral organs in hoplonemerteans (Nemertini), with a discussion of their function

  • Published:
Zoomorphology Aims and scope Submit manuscript

Summary

The fine structure of the cerebral organs is described in three species of monostiliferous hoplonemerteans. Amphiporus lactifloreus, Paranemertes peregrina and Tetrastemma candidum. There are two distinct groups of sensory cells in the cerebral organs of all three species. The ultrastructure of the sensory elements in these species is consistent with a chemoreceptive function of the dendrites. Incurrent and excurrent channels of the canal are postulated, based on the fine structure of the ciliary axonemes. Flow through the canal is such that each of the two groups of dendrites is downstream from a group of glandular cell outlets and upstream from a group of vesicular cells. It is suggested that the glandular, sensory and vesicular cells form a functional unit in which glandular cells secrete a coating material over the dendrites and vesicular cells actively remove this coating by endocytosis. Vesicular material is also found in glandular cells, where it probably arises in situ through crinophagy. There is no ultrastructural evidence that vesicular material is transferred to the vascular system. Small fibres containing dense vesicles are present among the ciliated cells and may represent an efferent nerve supply controlling the rate of flow through the canal.

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

  • Äkeson B (1958) A study of the nervous system of the Sipunculoideae. Undersökningar Över Öresund 23

  • Altner H, Prillinger L (1980) Ultrastructure of invertebrate chemoreceptors, thermoreceptors and hygroreceptors, and its functional significance. Int Rev Cytol 67:69–140

    Google Scholar 

  • Amerongen HM, Chia FS (1982) Behavioural evidence for a chemoreceptive function of the cerebral organs in Paranemertes peregrina Coe (Hoplonemertea: Monostilifera). J Exp Mar Biol Ecol 64:11–16

    Google Scholar 

  • Amerongen HM, Chia FS (1983) The role of nemertean cerebral organs in salinity stress tolerance re-examined in Paranemertes peregrina Coe (Hoplonemertea: Monostilifera). Mar Behav Physiol 10:1–22

    Google Scholar 

  • Bannister LH (1968) Fine structure of the sensory endings in the vomero-nasal organ of the slow-worm Anguis fragilis. Nature 217:275–276

    Google Scholar 

  • Bannister LH (1974) Possible functions of mucus at gustatory and olfactory surfaces. In: Poynder TM (ed) Transduction mechanisms in chemoreception. Information Retrieval Ltd London, pp 39–46

  • Barber VC (1968) The structure of mollusc statocysts, with particular reference to cephalopods. Symp Zool Soc London 23:37–62

    Google Scholar 

  • Barber VC (1974) Cilia in sense organs. In: Sleigh MA (ed) Cilia and flagella. Academic Press, London New York, pp 403–433

    Google Scholar 

  • Batson BS (1978) Ultrastructure of the anterior sense organs of adult Gastromermis boophthorae (Nematoda: Mermithidae). Tissue Cell 10:51–61

    Google Scholar 

  • Benjamin PR, Peat A (1971) On the structure of the pulmonate osphradium. II. Ultrastructure. Z Zellforsch 118:168–189

    Google Scholar 

  • Boeckh J (1981) Chemoreceptors: their structure and function. In: Laverack MS, Cosens DJ (eds) Sense organs. Blackie, London, pp 86–99

    Google Scholar 

  • Bostock H (1974) Diffusion and the frog EOG. In: Poynder TM (ed) Transduction mechanisms in chemoreception. Information Retrieval Ltd London, pp 27–36

  • Bürger O (1895) Die Nemertinen des Golfes von Neapel und der Angrenzenden Meeres-Abschnitte. Fauna Flora Golf Neapel 22:1–743

    Google Scholar 

  • Crisp M (1973) Fine structure of some prosobranch osphradia. Marine Biol 22:231–240

    Google Scholar 

  • Den Otter CJ (1981) Mechanisms of stimulus transduction in chemoreceptors. In: Laverack MS, Cosens DJ (eds) Sense organs. Blackie, Glasgow London, pp 186–215

    Google Scholar 

  • Dewoletzky R (1887) Das Seitenorgan der Nemertinen. Arb Zool Inst Univ Wien 7:233–280

    Google Scholar 

  • Dunlap H (1966) Oogenesis in the Ctenophora. PhD thesis, University of Washington, Seattle, Washington, USA

    Google Scholar 

  • Ferraris JD (1979) Histological study of secretory structures of nemerteans subjected to stress. II. Cerebral organs. Gen Comp Endocrinol 39:434–450

    Google Scholar 

  • Ferraris JD (1985) Putative neuroendocrine devices in the nemertina — an overview of structure and function. Am Zool 25:73–85

    Google Scholar 

  • Flock Ä (1967) Ultrastructure and function in the lateral line organs. In: Lateral line detectors. Indiana University Press, Bloomington, pp 163–197

    Google Scholar 

  • Flock Ä, Duvall AJ (1965) The ultrastructure of the kinocilium of the sensory cells in the inner ear and lateral line organs. J Cell Biol 25:1–8

    Google Scholar 

  • Garreau de Loubresse N (1980) Overloading, crinophagy and autophagy of the shell glands in a crustacean. Biol Cell 39:63–90

    Google Scholar 

  • Gibbons IR (1961) The relationship between the fine structure and direction of beat in gill cilia of a lamellibranch mollusc. J Biophys Biochem Cytol 11:179–205

    Google Scholar 

  • Graziedei PPC (1973) The ultrastructure of vertebrates olfactory mucosa. In: Friedmann I (ed) The ultrastructure of sensory organs. North-Holland, Amsterdam London. American Elsevier, New York, pp 267–305

    Google Scholar 

  • Keverne EB (1982) Chemical senses: smell. In: Barlow HB, Mollon JD (eds) The Senses Cambridge University Press, Cambridge London New York, pp 409–427

    Google Scholar 

  • Kipke S (1932) Studien über Regenerationserscheinungen bei Nemertinen. (Prostoma graecense Böhmig). Zool Jahrb Abt Allg Zool Physiol 51:1–66

    Google Scholar 

  • Kirsteuer E (1967) Marine benthonic nemerteans: how to collect and preserve them. Am Mus Novit 2290:1–10

    Google Scholar 

  • Lechenault H (1965) Neurosécrétion et osmorégulation chez les Lineidae (Hétéronémertes). CR Acad Sci [O] Paris 261:4868–4871

    Google Scholar 

  • Ling EA (1969) The structure and function of the cephalic organ of a nemertine Lineus ruber. Tissue Cell 1:503–524

    Google Scholar 

  • Ling EA (1970) Further investigations on the structure and function of the cephalic organs of a nemertine Lineus ruber. Tissue Cell 2:569–588

    Google Scholar 

  • Millott N (1968) The dermal light sense. Symp Zool Soc London 23:1–36

    Google Scholar 

  • Mozell MM (1966) The spatiotemporal analysis of odorants at the level of the olfactory receptor sheet. J Gen Physiol 50:25–41

    Google Scholar 

  • Mozell MM (1970) Evidence for a chromatographic model of olfaction. J Gen Physiol 56:46–63

    Google Scholar 

  • Okajima A (1953) Studies on the metachronal wave in Opalina. I. Electrical stimulation with the micro-electrode. Jpn J Zool 11:87–100

    Google Scholar 

  • Pearse BMF (1976) Clathrin: a unique protein associated with intracellular transfer of membrane by coated vesicles. Proc Nat Acad Sci USA 73:1255–1259

    Google Scholar 

  • Reisinger E (1926) Nemertini. Schnurwürmer. Biol Tiere Dtsch 17:7.1–7.24

    Google Scholar 

  • Richardson KC, Jarett L, Finke EH (1960) Embedding in epoxy resins for ultrathin sectioning in electron microscopy. Stain Technol 35:313–323

    Google Scholar 

  • Scharrer B (1941) Neurosecretion III. The cerebral organ of the nemerteans. J Comp Neurol 74:109–130

    Google Scholar 

  • Sleigh MA (1960) The form of beat in cilia of Stentor and Opalina. J Exp Biol 37:1–10

    Google Scholar 

  • Smith RE, Farquhar MG (1966) Lysosome function in the regulation of the secretory process in cells of the anterior pituitary gland. J Cell Biol 31:319–347

    Google Scholar 

  • Storch V, Riemann F (1973) Zur Ultrastruktur der Seitenorgane (Amphiden) des limnischen Nematoden Tobrilus aberrans (W. Schneider, 1925) (Nematoda, Enoplida). Z Morphol Tiere 74:163–170

    Google Scholar 

  • Venable JH, Coggeshall R (1965) A simplified lead citrate stain for use in electron microscopy. J Cell Biol 24:407–408

    Google Scholar 

  • Ward S, Thomson N, White JG, Brenner S (1975) Electron microscopical reconstruction of the anterior sensory anatomy of the nematode Caenorhabditis elegans. J Comp Neurol 160:313–338

    Google Scholar 

  • Welsch U, Storch V (1969) Über das Osphradium der prosobranchen Schnecken Buccinum undatum L. und Neptunea antiqua (L.). Z Zellforsch 95:317–330

    Google Scholar 

  • Wessenberg H (1966) Observations on cortical ultrastructure in Opalina. J Microsc 5:471–492

    Google Scholar 

  • West D (1978) Comparative ultrastructure of juvenile and adult nuchal organs of an annelid (Polychaeta: Opheliidae). Tissue Cell 10:243–257

    Google Scholar 

  • Whittle AC, Zahid ZR (1974) Fine structure of nuchal organs in some errant polychaetous annelids. J Morphol 144:167–184

    Google Scholar 

  • Willmer EN (1970) Cytology and Evolution 2nd ed. Academic Press, New York

    Google Scholar 

  • Wright BR (1974) Sensory structure of the tentacles of the slug, Arion ater (Pulmonata, Mollusca). 2. Ultrastructure of the free nerve endings in the distal epithelium. Cell Tissue Res 151:245–257

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Amerongen, H.M., Chia, F.S. Fine structure of the cerebral organs in hoplonemerteans (Nemertini), with a discussion of their function. Zoomorphology 107, 145–159 (1987). https://doi.org/10.1007/BF00312308

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00312308

Keywords

Navigation