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Life at low oxygen tensions: the behaviour and physiology of Nautilus pompilius and the biology of extinct forms

Published online by Cambridge University Press:  11 May 2009

M.J. Wells
Affiliation:
The Motupore Island Research Department, University of Papua New Guinea
J. Wells
Affiliation:
Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ.
R.K. O'Dor
Affiliation:
Department of Biology, Dalhousie University, Halifax, Nova Scotia, B3H 4J1, Canada.

Abstract

Nautilus can survive for long periods in water of very low oxygen content. Below a PO2 of around 25 mm Hg activity becomes intermittent, with brief periods of jet propulsion punctuating longer (typically 15–20 min) periods at rest. During these inactive periods ventilatory movements cease and the heartbeat slows to one or two cycles of very low amplitude per minute. The onset of an active period is heralded by an increase in heartbeat frequency and amplitude and a resumption of visible ventilatory movements. The large blood volume and very high oxygen affinity of the blood pigment apparently ensure that the animal accumulates sufficient oxygen during the resting intervals to fuel the brief active periods. Recovery, even after prolonged exposure to near anoxic conditions, is very rapid if the animal is exposed to well-aerated water. These capacities are not only related to a strategy of defence by withdrawal but would also allow Nautilus to exploit environments where the low oxygen content might limit competition from most fish and crustaceans. It is argued that a Nautilus-like physiology and behaviour could well have contributed to the success of extinct ectocochleate forms, living in oceans that were, by and large, less well oxygenated than now. The downward extension of oxygen-rich water and progressive elimination of hypoxic regions from the continental shelves during the Mesozoic may have contributed to the extinction of the ectocochleates by opening up the hitherto hypoxic environments, which they were adapted to exploit, to the more strictly aerobic high metabolic rate competitors and predators that eventually replaced them.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 1992

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References

Berry, W.B.N. & Wilde, P., 1984. Progressive ventilation of the oceans – an explanation for the distributions of the lower Paleozoic black shales. American Journal of Science, 278, 257275.CrossRefGoogle Scholar
Bourne, B.B., 1987. The circulatory system. In Nautilus: the biology and paleobiology of a living fossil (ed. W.B., Saunders and N.H., Landman), pp. 271279. New York: Plenum Press.CrossRefGoogle Scholar
Boyle, P.R., 1991. The care and management of cephalopods in the laboratory. Universities Federation for Animal Welfare Monograph. Longman Scientific and Technical: Harlow.Google Scholar
Chamberlain, J. A. Jr & Moore, W.A. Jr, 1982. Rupture strength and flow rate of Nautilus siphuncular tube. Paleobiology, 8, 408425.CrossRefGoogle Scholar
Cloud, P., 1983. The biosphere. Scientific American, 249(3), 132144.CrossRefGoogle Scholar
Denton, E.J. & Gilpin-Brown, J.B., 1966. On the buoyancy of the pearly Nautilus. Journal of the Marine Biological Association of the United Kingdom, 46, 723759.CrossRefGoogle Scholar
Hayasaka, S., Kimihiko, O., Tanabe, K., Saisho, T. & Shinomiya, A., 1987. On the habitat of Nautilus pompilius in Tanon Strait (Philippines) and the Fiji Islands. In Nautilus: the biology and paleobiology of a living fossil (ed. W.B., Saunders and N.H., Landman), pp. 179200. New York: Plenum Press.CrossRefGoogle Scholar
Holland, H.D., 1984 The chemical evolution of the atmosphere and oceans. Princetown: Princetown University Press.CrossRefGoogle Scholar
Johansen, K., Redmond, J.R. & Bourne, G.B., 1978. Respiratory exchange and transport of oxygen in Nautilus pompilius. Journal of Experimental Zoology, 205, 2736.CrossRefGoogle Scholar
Krogh, A., 1919. The rate of diffusion of gases through animal tissues, with some remarks on the coefficient of invasion. Journal of Physiology, 52, 391408.CrossRefGoogle ScholarPubMed
Lehmann, U., 1981 The ammonites: their life and their world. Cambridge: Cambridge University Press.Google Scholar
Mangold, K., Bidder, A.M. & Portman, A., 1989. Organisation générates des Céphalopodes. In Traité de Zoologie, torn 5, fasc 4, Céphalopodes (ed. K., Mangold), pp. 769. Paris: Masson.Google Scholar
O'dor, R.K., 1982. Respiratory metabolism and swimming performance of the squid, Loligo opalescens. Canadian Journal of Fisheries and Aquatic Sciences, 39, 580587.CrossRefGoogle Scholar
O'dor, R.K., Wells, M.J. & Wells, J., 1990. Speed, jet pressure and oxygen consumption relationships in free-swimming Nautilus. Journal of Experimental Biology, 154, 383396.CrossRefGoogle Scholar
Packard, A., 1972. Cephalopods and fish: the limits of convergence. Biological Reviews, 47, 241307.CrossRefGoogle Scholar
Redmond, J.R., 1987. Respiratory physiology. In Nautilus: the biology and paleobiology of a living fossil (ed. W.B., Saunders and N.H., Landman), pp. 305312. New York: Plenum Press.CrossRefGoogle Scholar
Saunders, W.B., Spinosa, C. & Davis, L.E., 1987. Predation on Nautilus. In Nautilus: the biology and paleobiology of a living fossil (ed. W.B., Saunders and N.H., Landman), pp. 201212. New York: Plenum Press.CrossRefGoogle Scholar
Teichert, C., 1967. Major features of cephalopod evolution. In Essays in paleontology and stratigraphy (ed. C., Teichert and E., Yochelson), pp. 162210. Kansas: Special publication, Department of Geology, University of Kansas.Google Scholar
Ward, P.D., 1979. Cameral liquid in Nautilus and ammonites. Palaeobiology, 5, 4049.CrossRefGoogle Scholar
Ward, P.D., 1987. The natural history of Nautilus. Boston: Allen & Unwin.Google Scholar
Webber, D.M. & O'dor, R.K., 1985. Respiration and swimming performance of the short-finned squid, Illex illecebrosus. Scientific Council Studies. Northwest Atlantic Fisheries Organisation, 9, 133138.Google Scholar
Wells, M.J., 1987. Oxygen uptake and the effect of feeding in Nautilus. Veliger, 30, 6975.Google Scholar
Wells, M.J. & O'dor, R.K., 1992, in press. Jet propulsion and the evolution of the Cephalopods. Bulletin of Marine Science.Google Scholar
Wells, M.J. & Wells, J., 1983. The circulatory response to acute hypoxia in Octopus. Journal of Experimental Biology, 104, 5971.CrossRefGoogle Scholar
Wells, M.J. & Wells, J., 1984. The effects of reducing gill area on the capacity to regulate oxygen uptake and on metabolic scope in a cephalopod. Journal of Experimental Biology, 108, 393401.CrossRefGoogle Scholar
Wells, M.J. & Wells, J., 1985. Ventilation and oxygen uptake by Nautilus. Journal of Experimental Biology, 118, 297312.CrossRefGoogle Scholar
Wilde, P. & Berry, W.B.N., 1984. Destabilisation of the ocean density structure and its significance for marine ‘extinction’ events. Paleogeography, Paleoclimatology and Paleoecology, 48, 143162.CrossRefGoogle Scholar
Young, J.Z., 1965. The central nervous system of Nautilus. Philosophical Transactions of the Royal Society of London (B), 249, 125.Google Scholar
Zann, L.P., 1984. The rhythmic activity of Nautilus pompilius with notes on its ecology and behaviour in Fiji. Veliger, 27, 1928.Google Scholar