Reviews in Fish Biology and Fisheries

, Volume 17, Issue 2–3, pp 385–399

How long would it take to become a giant squid?

Research Paper

Abstract

Laboratory and field studies suggest that cephalopod growth occurs rapidly and is linked to temperature throughout a short life span. For giant squid such as Architeuthis, a paucity of size-at-age data means that growth is only inferred from isolated field specimens, based on either statoliths or isotopic analyses of tissue. In this study we apply simple growth models to obtain projections of the life span required to achieve the Architeuthis average body mass in scenarios which include an energy balance between rates of food intake and expenditure on growth and metabolism. Although the analysis shows that a wide range for the estimated life span is possible, energy conservation suggests that achievement of a larger size would be assisted by slower exponential growth early on. The results are compared with a sparse set of size-at-age data obtained from male and female Architeuthis wild specimens and possibly hint at some behavioural differences between males and females.

Keywords

Feeding and metabolic rates Simple two phase growth model Energy balance Architeuthis Giant squid Cephalopod growth Growth models 

References

  1. Arkhipkin AI, Bizikov VA (1997) Statolith shape and microstructure in studies in systematics, age and growth in planktonic paralarvae of gonatid squids (Cephalopoda, Oegopsida) from the western Bering Sea. J Plankton Res 19:1993–2030CrossRefGoogle Scholar
  2. Arkhipkin AI, Bizikov VA, Krylov VV, Nesis KN (1996) Distribution, stock structure and growth of the squid Berryteuthis magister (Berry, 1913) (Cephalopoda, Gonatidae) during summer and fall in the western Berring Sea. Fish Bull 94:1–30Google Scholar
  3. Arkhipkin AI, Bizikov VA, Verkhunov AV (1998) Distribution and growth in juveniles of the squid Berryteuthis magister (Cephalopoda, Gonaditae) in the western Berring Sea. Sarsia 83:45–54Google Scholar
  4. Bigelow KA (1992) Age and growth in paralarvae of the mesopelagic squid Abralia trigonurabased on daily growth increments in statoliths. Mar Ecol Prog Ser 82:31–40Google Scholar
  5. Bigelow KA, Landgraf KC (1993) Hatch dates and growth of Ommastrephes bartramii paralarvae from Hawaiian waters as determined from statolith analysis. In: Okutani T, O’Dor RK, Kubodera T (eds) Recent advances in cephalopod fisheries biology. Tokai University Press, Tokyo, pp 15–24Google Scholar
  6. Erickson GM, Makovicky PJ, Currie PJ, Norell MA, Yerby SA, Brochu CA (2004) Gigantism and comparative life-history parameters of tyrannosaurid dinosaurs. Nature 430:772–775PubMedCrossRefGoogle Scholar
  7. Forsythe JW, van Heukelem WF (1987) Growth. In: Boyle PR (ed), Cephalopod Life Cycles vol II, Comparative reviews. Academic Press, London, pp 135–156Google Scholar
  8. Forsythe JW (1993) A working hypothesis of how seasonal temperature change may impact the field growth of young cephalopods. In: Okutani T, O’Dor RK, Kubodera T (eds) Recent Advances in Cephalopod Fisheries Biology. Tokai University Press, Tokyo, pp 133–143Google Scholar
  9. Gauldi RW, West IF (1994) Statocyst, statolith, and age estimation of the giant squid Architeuthis kirki. Veliger 37:93–109Google Scholar
  10. Grist EPM (2000) A circle map for a phytoplanktonic life cycle. Int J Bifurcation Chaos. 10(2):325–344CrossRefGoogle Scholar
  11. Grist EPM, des Clers S (1999) Seasonal and genotypic influences on life cycle synchronisation: further insights from annual squid. Ecol Modell 115:149–163CrossRefGoogle Scholar
  12. Grist EPM, Jackson GD (2004) Energy balance as a determinant of two-phase growth in cephalopods. Mar Freshw Res 55:395–401CrossRefGoogle Scholar
  13. Hatfield EMC (1991) Post recruit growth of the Patagonian squid Loligo gahi (D’Orbigny). Bull Mar Sci 49:349–361Google Scholar
  14. Hatfield EMC, Hanlon RT, Forsythe JW, Grist EPM (2001) Laboratory testing of a growth hypothesis for juvenile squid Loligo pealii(Cephalopoda: Loliginidae). Can J Fish Aquat Sci 58:845–857CrossRefGoogle Scholar
  15. Jackson GD (1997) Age, growth and maturation of the deepwater squid Moroteuthis ingens (Cephalopoda: Onychoteuthidae) in New Zealand waters. Polar Biol 17:268–274CrossRefGoogle Scholar
  16. Jackson GD, O’Dor RK (2001) Time, space and the ecophysiology of squid growth, life in the fast lane. Vie Milieu 51:205–215Google Scholar
  17. Jackson GD, Domeier ML (2003) The effects of an extraordinary El Niño/La Niña event on the size and growth of the squid Loligo opalescens off Southern California. Mar Biol 142:925–935Google Scholar
  18. Jackson GD, Lu CC, Dunning M (1991) Microstructural growth rings in the statoliths of the giant squid Architeuthis. Veliger 34:331–334Google Scholar
  19. Jackson GD, McKinnon JF, Lalas C, Ardern R, Buxton NG (1998) Food spectrum of the deepwater squid Moroteuthis ingens (Cephalopoda: Onychoteuthidae) in New Zealand waters. Polar Biol 20:56–65CrossRefGoogle Scholar
  20. Landman NH, Coshran JK, Cerrato R, Mak J, Roper CFE, Lu CC (2004) Habitat and age of the giant squid (Architeuthis sanctipauli) inferred from isotopic analyses. Mar Biol 144:685–691CrossRefGoogle Scholar
  21. Lipinski M (1997) Morphology of giant squid Architeuthis statoliths. S Afr J Mar Sci 18:299–303Google Scholar
  22. Lordan C, Collins MA, Perales-Raya C (1998) Observations on morphology, age and diet of three Architeuthis caught off the West Coast of Ireland in 1995. J Mar Biol Assoc UK 78:9003–9917Google Scholar
  23. McNeil Alexander R (1999) Minimal metabolism (section 2.4 pages 26–32). In: Energy for animal life. Oxford University PressGoogle Scholar
  24. Moltschaniwskyj NA (2004) Understanding the process of growth in cephalopods. Mar Freshw Res 55:379–386CrossRefGoogle Scholar
  25. O’Dor RK, Wells MJ (1987) Energy and nutrient flow. In: PR Boyle (ed) Cephalopod life cycles vol II, Comparative reviews. Academic Press, London, pp 109–133Google Scholar
  26. O’Dor RK, Aitken J, Jackson GD (2005) Energy balance growth models: applications to cephalopods. Phuket Mar Bio Cent Res Bull 66:329–336Google Scholar
  27. Perez A, O’Dor RK (2000) Critical transitions in early life histories of short finned squid ilex illecebrocus as constructed from gladius growth. Journal of the Marine Biological Association of the UK 80(3):509–514CrossRefGoogle Scholar
  28. Seber GAF, Wild CJ (1989) Nonlinear Regression. John Wiley and Sons Inc., New YorkGoogle Scholar
  29. Seibel BA, Thuesen EV, Childress JJ, Gorodezky LA (1997) Decline in pelagic cephalopod metabolism with habitat depth reflects differences in locomotory efficiency. Biol Bull 192:267–278CrossRefGoogle Scholar
  30. Seibel BA, Thuesen EV, Childress JJ (2000) Light limitation on predator-prey interactions: consequences for metabolism and locomotion of deep sea cephalopods. Biol Bull 198:284–298PubMedCrossRefGoogle Scholar
  31. Toms JD, Lesperance ML (2003) Piecewise regression: a tool for identifying ecological thresholds. Ecology 84(8):2034–2041CrossRefGoogle Scholar
  32. Villaneuva R (2000) Effect of temperature on statolith growth of the European squid Loligo vulgaris during early life. Mar Biol 136:449–460CrossRefGoogle Scholar
  33. von Bertalanffy L (1957) Quantitative laws in metabolism and growth. Q Rev Biol 32:217–231CrossRefGoogle Scholar
  34. Yatsu A, Mori J (2000) Early growth of the autumn cohort of neon flying squid, Ommastrephes bartramii, in the North Pacific Ocean. Fish Res 45:189–194CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, Inc. 2007

Authors and Affiliations

  1. 1.CSIRO Marine and Atmospheric ResearchHobartAustralia
  2. 2.Institute of Antarctic and Southern Oceanic StudiesUniversity of TasmaniaHobartAustralia

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