Hostname: page-component-848d4c4894-p2v8j Total loading time: 0.001 Render date: 2024-05-14T15:29:27.732Z Has data issue: false hasContentIssue false

The escal light gland of the deep-sea anglerfish Haplophryne mollis (Pisces: Ceratioidei) with observations on luminescence control

Published online by Cambridge University Press:  09 October 2019

Peter J. Herring
Affiliation:
Institute of Oceanographic Sciences Deacon Laboratory, Brook Road, Wormley, Godalming, Surrey, GU85UB
Ole Munk
Affiliation:
Zoological Institute, Cell Biological and Anatomical Laboratory, University of Copenhagen, Denmark

Abstract

The escal light gland of three different-sized specimens of the deep-sea anglerfish Haplophryne mollis (family Linophrynidae) has been examined by light and electron microscopy. The light gland has a central cavity, with diverging branched ducts which ramify into numerous tightly-packed radial tubules. In the two largest specimens all glandular lumina contain symbiotic bacteria. Except for a thin-walled part of the typical radiating tubules, the epithelial walls of the light gland are of a uniform structure, consisting of flattened basal cells, situated next to the basal lamina, and tall cells extending to the lumen.

In the smallest specimen examined the various parts of the light gland were not fully differentiated and only a very few symbiotic bacteria were present; its glandular epithelium differed from that of the two larger specimens by containing many goblet cells, the secretion of which may be important for the initial establishment of the right strain of symbiotic bacteria

Observations on the luminescence of live specimens have shown that the light emission can be rapidly modulated from within the esca. The in vivo flash kinetics are considerably slower than those of Dolopichthys longicornis, but similar to those of both the caruncle exudate of Ceratias holboelli and in vitro anglerfish bacterial luciferase.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bassot, J.-M., 1966. On the comparative morphology of some luminous organs. In Bioluminescence in progress (ed. Johnson, F.H. and Haneda, Y.), pp. 557610. Princeton: Princeton University Press.Google Scholar
Bertelsen, E., 1951. The ceratioid fishes. Dana Report, no. 39, 1276.Google Scholar
Bertelsen, E. & Krefft, G., 1988. The ceratioid family Himantolophidae (Pisces, Lophiiformes). Steenstrupia, 14, 989.Google Scholar
Bertelsen, E. & Pietsch, T.W., 1977. Results of the research cruises of FRV ‘Walther Herwig’ to South America. XLVII. Ceratioid anglerfishes of the family Oneirodidae collected by the FRV ‘Walther Herwig’. Archiv für Fischereiwissenschaft, 27, 171189.Google Scholar
Bowlby, Mr., Widder, E.A. & Case, J.F., 1990. Patterns of stimulated bioluminescence in two pyrosomes (Tunicata: Pyrosomatidae). Biological Bulletin. Marine Biological Laboratory, Woods Hole, 179, 340350.Google Scholar
Dahlgren, U., 1928. The bacterial light organ of Ceratias . Science, New York, 68, 6566.Google Scholar
Hansen, K. & Herring, P.J., 1977. Dual bioluminescent systems in the anglerfish genus Linophryne (Pisces: Ceratioidea). Journal of Zoology, 182, 103124.Google Scholar
Haygood, M.G., 1993. Light organ symbioses in fishes. Critical Reviews in Microbiology, 19, 191216.Google Scholar
Haygood, M.G. & Distel, D.L., 1993. Bioluminescent symbionts of flashlight fishes and deep-sea anglerfishes form unique lineages related to the genus Vibrio . Nature, London, 363(6425), 154156.Google Scholar
Herring, P.J., 1983. The spectral characteristics of luminous marine organisms. Proceedings of the Royal Society (B), 220, 183217.Google Scholar
Herring, P.J., 1993. Light genes will out. Nature, London, 363(6425), 110111.Google Scholar
Herring, P.J. & Morin, J.G., 1978. Bioluminescence in fishes. In Bioluminescence in action(ed. Herring, P.J.), pp. 273329. London: Academic Press.Google Scholar
Hulet, W.H. & Musil, G., 1968. Intracellular bacteria in the light organ of the deep sea angler fish, Melanocetus murrayi . Copeia, 1968, 506512.Google Scholar
Leisman, G., Cohn, D.H. & Nealson, K.H., 1980. Bacterial origin of luminescence in marine animals. Science, New York, 208, 12711273.Google Scholar
Mackie, G.O. & Bone, Q., 1978. Luminescence and associated effector activity in Pyrosoma (Tunicata: Pyrosomida). Proceedings of the Royal Society (B), 202, 483495.Google Scholar
McFall-Ngai, M.J. & Ruby, E.G., 1991. Symbiont recognition and subsequent morphogenesis as early events in an animal-bacterial mutualism. Science, New York, 254, 14911494.Google Scholar
Montgomery, M.K. & McFall-Ngai, M.J., 1993. Embryonic development of the light organ of the sepiolid squid Euprymna scolopes Berry. Biological Bulletin. Marine Biological Laboratory, Woods Hole, 184, 296308.Google Scholar
Munk, O., 1988. Glandular tissue of escal light organ in the deep-sea anglerfish Oneirodes eschrichti (Pisces, Ceratioidei). A light and electron microscopic study. Videnskabelige Meddelelser fra Dansk Naturhistorisk Forening i Kjøbenhavn, 147, 93120.Google Scholar
Munk, O. & Bertelsen, E., 1980. On the esca light organ and its associated light-guiding structures in the deep-sea anglerfish Chaenophryne draco (Pisces, Ceratioidei). Videnskabelige Meddelelser fra Dansk Naturhistorisk Forening i Kjøbenhavn, 142, 103129.Google Scholar
Munk, O. & Bertelsen, E., 1983. Histology of the attachment between the parasitic male and the female in the deep-sea anglerfish Haplophryne mollis (Brauer, 1902) (Pisces, Ceratioidei). Videnskabelige Meddelelser fra Dansk Naturhistorisk Forening i Kjøbenhavn, 144, 4974.Google Scholar
O'day, W.T., 1974. Bacterial luminescence in the deep-sea anglerfish Oneirodes acanthias (Gilbert, 1915). Contributions in Science. Los Angeles County Museum of Natural History, no. 255, 112.Google Scholar
Whitear, M., 1986. The skin of fishes including cyclostomes: epidermis. In Biology of the integument, vol. 2 (ed. Bereiter-Hahn, J. et al.), pp. 838. Berlin: Springer Verlag.Google Scholar