Skip to main content
Log in

Effect of temperature on laboratory growth, reproduction and life span of Octopus bimaculoides

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Laboratory culture of 40 Octopus bimaculoides from April 1982 to August 1983 through the full life cycle at 18°C vs 23°C provided information on the growth, reproductive biology and life span of this California littoral octopus. At 18°C, the cephalopods grew from a hatchling size of 0.07 g to a mean of 619 g in 404 d; the largest individual was 872 g. Octopuses cultured at 23°C reached their highest mean weight of 597 g in 370 d; the largest individual grown at this temperature was 848 g after 404 d. Growth data revealed a two-phase growth pattern: a 5 mo exponential phase followed by a slower logarithmic (power function) phase until spawning. At 5 mo octopuses grown at 23°C were over three times larger than their 18°C siblings. However, beyond 6.5 mo, growth rates were no higher at 23°C than at 18°C. At 13.5 mo, the mean weight of the 18°C group surpassed that of the 23°C group. The slope of the length/weight (L/W) relationship was significantly different for the two temperature regimes, with the 23°C octopuses weighing 18% less than their 18°C siblings at a mantle length of 100 mm. Females weighed more than males at any given mantle length. Males grew slightly larger and matured before females. The L/W relationship indicated isometric body growth throughout the life cycle. Higher temperature accelerated all aspects of reproductive biology and shortened life span by as much as 20% (from approximately 16 to 13 mo). O. bimaculoides has one of the longest life cycles among species with large eggs and benthic hatchlings. Extrapolations to field growth are made, and the possible effects of temperature anomalies such as El Niño are discussed.

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

Literature cited

  • Ambrose, R. F. (1984). Food preferences, prey availability, and the diet of Octopus bimaculatus Verrill. J. exp. mar. Biol. Ecol. 77: 29–44

    Google Scholar 

  • Ambrose, R. F. (1986). Effects of octopus predation on motile invertebrates in a rocky subtidal community. Mar. Ecol. Prog. Ser. 30: 261–273

    Google Scholar 

  • Ambrose, R. F. (1988). Population dynamics of Octopus bimaculatus: influence of life history patterns synchronous reproduction and recruitment. Malacologia 29 (1): 23–29

    Google Scholar 

  • Boletzky, S. von (1974). The “larvae” of Cephalopoda: a review. Thalassia jugosl. 10: 45–76

    Google Scholar 

  • Boyle, P. R. (ed.) (1983). Cephalopod life cycles, Vol. I. Species accounts. Academic Press, London

    Google Scholar 

  • Boyle, P. R. (ed.) (1987) Cephalopod life cycles, Vol. II, Comparative reviews. Academic Press, London

    Google Scholar 

  • Brody, S. (1945). Bioenergetics and growth with special reference to the efficiency complex in domestic animals. Hafner Press, New York

    Google Scholar 

  • Brown, M. E. (1957). Experimental studies on growth. In: Brown, M. E. (ed.) The physiology of fishes, Vol. 1, Metabolism. Academic Press, New York, p. 361–400

    Google Scholar 

  • DeRusha, R. H., Forsythe, J. W., Hanlon, R. T. (1988). Laboratory growth, reproduction and life span of the Pacific pygmy octopus, Octopus digueti. Pacif. Sci. 41: 51–59

    Google Scholar 

  • Dorsey, E. M. (1976). Natural history and social behavior of Octopus rubescens Berry. Master's thesis, University of Washington, Friday Harbor

  • Forsythe, J. W. (1984). Octopus joubini (Mollusca: Cephalopoda): a detailed study of growth through the full life cycle in a closed seawater system. J. Zool., Lond. 202: 393–417

    Google Scholar 

  • Forsythe, J. W., Hanlon, R. T. (1988). Behavior, body patterning and reproductive biology of Octopus bimaculoides from California. Malacologia 29 (1): 40–56

    Google Scholar 

  • Forsythe, J. W., Van Heukelem, W. F. (1987). Cephalopod growth. In: Boyle, P. R. (ed.) Cephalopod life cycles, Volume II, Comparative reviews. Academic Press, London, p. 135–155

    Google Scholar 

  • Gould, S. J. (1966). Allometry and size in ontogeny and phylogeny. Biol. Rev. 41: 587–640

    Google Scholar 

  • Guerra, A. (1979). Fitting a von Bertalanffy expression to Octopus vulgaris growth. Investigación pesq. 43: 319–329

    Google Scholar 

  • Hanlon, R. T. (1983). Octopus briareus. In: Boyle, P. R. (ed.) Cephalopod life cycles, Vol. I. Species accounts. Academic Press, London, p. 251–266

    Google Scholar 

  • Hanlon, R. T., Forsythe, J. W. (1985). Advances in the laboratory culture of octopuses for biomedical research. Lab. Anim. Sci. 35: 33–40

    Google Scholar 

  • Hartwick, B. (1983). Octopus dofleini. In: Boyle, P. R. (ed.) Cephalopod life cycles, Vol. 1, Species accounts. Academic Press, London, p. 277–291

    Google Scholar 

  • Hendrix, J. P., Jr., Hulet, W. H., Greenberg, M. J. (1981). Salinity tolerance and the responses to hypoosmotic stress of the bay squid Lolliguncula brevis, a euryhaline cephalopod mollusc. Comp. Biochem. Physiol. 69A: 641–648

    Google Scholar 

  • Hochberg, F. G., Jr., Fields, W. G. (1980). The squids and octopuses. In: Morris, R. H., Abbott, D. P., Haderlie, E. C. (eds.) Intertidal invertebrates of California, Chapter 17: Cephalopoda. Stanford, Stanford University Press, p. 429–444 and P133-P136

    Google Scholar 

  • Mangold, K. (1983). Octopus vulgaris. In: Boyle, P. R. (ed.) Cephalopod life cycles, Vol. 1, Species accounts. Academic Press, London, p. 335–364

    Google Scholar 

  • McGowan, J. A. (1984). The California El Niño, 1983. Oceanus 27 (2): 48–51

    Google Scholar 

  • Packard, A. (1972). Cephalopods and fish: the limits of convergence. Biol. Rev. 47: 241–307

    Google Scholar 

  • Pascual, E. (1978). Crecimiento y alimentación de tres generaciónes de Sepia officinalis en cultivo. (Growth and feeding of three generations of lab-reared Sepia officinalis). Investigación pesq. 42: 421–442

    Google Scholar 

  • Pickford, G. E., McConnaughey, B. H. (1949). The Octopus bimaculatus problem: a study in sibling species. Bull. Bingham oceanogr. Coll. 12(4): 1–66

    Google Scholar 

  • Richard, A. (1966). Action de la temperature sur l'evolution genitale de Sepia officinalis L. C. r. hebd. Séanc. Acad. Sci., Paris 263: 1998–2001

    Google Scholar 

  • Ricker, W. E. (1979). Growth rates and models. Fish Physiol. 8: 677–743

    Google Scholar 

  • Van Heukelem, W. F. (1976). Growth, bioenergetics and life-span of Octopus cyanea and Octopus maya. Ph.D. dissertation, University of Hawaii, Honolulu

  • Van Heukelem, W. F. (1979). Environmental control of reproduction and life span in Octopus: an hypothesis. In: Stancyk, S. E. (ed.) Reproductive ecology of marine invertebrates. University of South Carolina Press, Columbia, p. 123–133

    Google Scholar 

  • Wells, M. J., Wells, J. (1970). Observations on the feeding, growth rate and habits of newly settled Octopus cyanea. J. Zool., Lond. 161: 65–74

    Google Scholar 

  • Young, R. E., Harman, R. F. (1988). “Larva”, “paralarva” and “subadult” in cephalopod terminology. Malacologia 29 (1): 201–207

    Google Scholar 

  • Zar, J. H. (1974). Biostatistical analysis. Prentice-Hall Inc., Englewood Cliffs

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Communicated by R. S. Carney, Baton Rouge

Rights and permissions

Reprints and permissions

About this article

Cite this article

Forsythe, J.W., Hanlon, R.T. Effect of temperature on laboratory growth, reproduction and life span of Octopus bimaculoides . Marine Biology 98, 369–379 (1988). https://doi.org/10.1007/BF00391113

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00391113

Keywords

Navigation