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Ontogeny of aggressive behaviour in schools of yellowtail, Seriola quinqueradiata

  • Yoshitaka Sakakura
  • Katsumi Tsukamoto
Part of the Developments in environmental biology of fishes book series (DEBF, volume 19)

Synopsis

We studied ontogenetic changes in social interactions, especially in aggressive behaviour of the migratory marine yellowtail, Seriola quinqueradiata (Carangidae), and compared these to morphological and physiological changes. No agonistic interactions were observed during the larva period until 10 mm in total length (TL), at approximately 20 days after hatching. Typical shivering behaviour with ‘J-posture’ was observed during metamorphosis, when fin rays and calcification of vertebra were completed and there was an increase of tissue thyroid hormone. The onset of aggressive behaviour was just after metamorphosis to the juvenile period, and coincided with a significant increase in tissue cortisol levels. The onset of schooling behaviour was at 12 mm TL, slightly after the onset of aggressive behaviour. From observations of individual aggressive behaviour within juvenile schools, we found three categories of social rank: dominants (10–20%), intermediates (10–20%), and subordinates (60–80%). There was an inverse relationship between social rank and cortisol concentration. Otoliths of dominant fish in 8 experimental groups were labeled and the fish were returned to their groups. Six labeled dominants appeared after 1 day and three after 1 week rearing, respectively, indicating that social rank was maintained for at least 1 week (binomial distribution, p < 0.05). Dominants were larger than subordinates after 1 day rearing, whereas dominants were smaller after 1 week rearing. From long-term rearing experiments using individual otolith marking, larvae that showed the ‘J-posture’ more frequently tended to become dominants after metamorphosis, indicating a positive correlation between the ‘J-posture’ and aggressive behaviour. Synthesizing all results from behavioural experiments, we generated a behavioural model for the triggering mechanism of aggressive behaviour and size selection of school members.

Key words

social rank schooling behaviour cannibalism otolith 

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References cited

  1. Abbott, J.C., R.L. Dunbrack & C.D. Orr. 1985. The interaction of size and experience in dominance relationships of juvenile steelhead trout (Salmo gairdneri). Behaviour 92: 241–253.Google Scholar
  2. Anraku, M. & M. Azeta. 1965. The feeding habits of larval and juveniles of yellowtail, Seriola quinqueradiata Temminck et Schlegel, associated with floating seaweeds. Bull. Seikai Reg. Fish. Res. Lab. 33: 14–15.Google Scholar
  3. Baton, E.K. 1984. Reflections on some decisive events in the early life of fishes. Trans. Amer. Fish. Soc. 113: 178–185.CrossRefGoogle Scholar
  4. Bond, C.E. 1979. Behavior. pp. 425–453. In: C.E. Bond (ed.) Biology of Fishes, Saunders College Publishing, Philadelphia.Google Scholar
  5. Breder, C.M. 1954. Equations descriptive of fish schools and other animal aggregations. Ecology 35: 361–370.CrossRefGoogle Scholar
  6. Brothers, E.B. 1984. Otolith studies. pp. 50–57. In: H.G. Moser, W.J. Richards, D.M. Cohen, M.P. Fahay, A.W.J. Kendall & S.L. Richardson (ed.) Brothers, E.B. 1, Lawrence.Google Scholar
  7. Chantanachookhin, C., T. Seikai & M. Tanaka. 1991. Comparative study of the ontogeny of the lymphoid organs in three species of marine fish. Aquaculture 99: 143–155.CrossRefGoogle Scholar
  8. Duncan, D.B. 1955. Multiple range and multiple F tests. Biometrics 11: 1–42.CrossRefGoogle Scholar
  9. Ejike, C. & C.B. Schreck. 1980. Stress and social hierarchy rank in coho salmon. Trans. Amer. Fish. Soc. 109: 423–426.CrossRefGoogle Scholar
  10. Elwood, R.W. & C.J. Rainey. 1983. Social organization and aggression within small groups of female Siamese fighting fish, Betta splendens. Aggressive Behay. 9: 303–308.CrossRefGoogle Scholar
  11. Fukuhara, O. 1992. Study on the development of functional morphology and behaviour of the larvae of eight commercially valuable teleost fishes. Contributions to the Fisheries Researches in the Japan Sea Block 25: 1–122.Google Scholar
  12. Fukuhara, O., T. Nakagawa & T. Fukunaga. 1986. Larval and juvenile development of yellowtail reared in the laboratory. Bull. Japan. Soc. Sci. Fish. 52: 2091–2098.CrossRefGoogle Scholar
  13. Hamilton, W.D. 1971. Geometry for the selfish herd. J. Theor. Biol. 31: 295–311.PubMedCrossRefGoogle Scholar
  14. Hiroi, J., Y. Sakakura, M. Tagawa, T. Seikai & M. Tanaka. 1997. Developmental changes in low-salinity tolerance and responses of prolactin, cortisol and thyroid hormones to low-salinity environment in larvae and juveniles of Japanese flounder, Paralichthys olivaceus. Zoological Science 14: 987–992.CrossRefGoogle Scholar
  15. Ichihara, K. 1990. Statistics for bioscience. Nankoudo, Tokyo. 378 pp. (in Japanese).Google Scholar
  16. Imaizumi, K. 1993. Recent progress of Japan Sea-Farming Association in marine finfish hatchery activities. pp. 173–177. In: C.-S. Lee, M.-S. Su & I.C. Liao (ed.) Finfish Hatchery in Asia, Proceedings of Finfish Hatchery in Asia ‘81,3, Tungkang Marine Labolatory TFRI and The Oceanic Institute, Tungkang.Google Scholar
  17. Inui, Y. & S. Miwa. 1985. Thyroid hormone induces metamorpho- sis of flounder larvae. Gen. Comp. Endocrinol. 60: 450–454.PubMedCrossRefGoogle Scholar
  18. Jesus, E.G.D., T. Hirano & Y. Inui. 1991. Changes in cortisol and thyroid hormone concentrations during early development and metamorphosis in the Japanese flounder, Paralichthys olivaceus. Gen. Comp. Endocrinol. 82: 369–376.CrossRefGoogle Scholar
  19. Jesus, E.G.D., Y. Inui & T. Hirano. 1990. Cortisol enhances the stimulating action of thyroid hormones on dorsal fin-ray resorption of flounder larvae in vitro. Gen. Comp. Endocrinol. 79: 167–173.PubMedCrossRefGoogle Scholar
  20. Kendall, A.W.J., E.H. Ahlström & H.G. Moser. 1984. Early life history stages of fishes and their characters. pp. 11–22. In: H.G. Moser, W.J. Richards, D.M. Cohen, M.P. Fahay, A.W.J. Kendall & S.L. Richardson (ed.) Kendall, A.W.J., E.H. Ahlström & H.G. Moser. 1, Lawrence.Google Scholar
  21. Koshio, S., Y. Sakakura, Y. Lida, K. Tsukamoto, T. Kida & K. Dabrowski. 1997. The effect of vitamin C intake on schooling behavior of amphidromous fish, ayu Plecoglossus altivelis. Fish. Sci. 63: 619–624.Google Scholar
  22. Magurran, A.E. 1990. The adaptive significance of schooling as an anti-predator defense in fish. Ann. Zool. Fennici 27: 51–66.Google Scholar
  23. Magurran, A.E. 1993. Individual differences and alternative behaviours. pp. 441–477. In: T.J. Pitcher (ed.) Behaviour of Teleost Fishes, Chapman & Hall, London.CrossRefGoogle Scholar
  24. Masuda, R. & K. Tsukamoto. 1998. The ontogeny of schooling behaviour in the striped jack. J. Fish Biol. 52: 483–493.CrossRefGoogle Scholar
  25. Masuda, R. & K. Tsukamoto. 1999. School formation and concurrent developmental changes in carangid fish with reference to dietary conditions. Env. Biol. Fish. 56: 243–252 (this volume).Google Scholar
  26. May, R.C. 1974. Larval mortality in marine fishes and the critical period concept. pp. 3–19. In: J.H.S. Blaxter (ed.) The Early Life History of Fish, Springer-Verlag, Berlin.CrossRefGoogle Scholar
  27. Noakes, D.L.G. 1978. Social behaviour as it influences fish production. pp. 360–382. In: S.D. Gerking (ed.) Ecology of Freshwater Fish Production, Blackwell, Oxford.Google Scholar
  28. Noakes, D.L.G. & J.-G.J. Godin. 1988. Ontogeny of behavior and concurrent developmental changes in sensory systems in teleost fishes. pp. 345–395. In: W.S. Hoar & D.J. Randall (ed.) Fish Physiology, Volume 6, Academic Press, San Diego.Google Scholar
  29. Noakes, D.L.G., J.F. Leatherland. 1977. Social dominance and interrenal cell activity in rainbow trout, Salmo gairdneri (Pisces, Salmonidae). Env. Biol. Fish. 2: 131–136.CrossRefGoogle Scholar
  30. Oliveira, R.F. & V.C. Almada. 1996. On the (in)stability of dominance hierarchies in the cichlid fish Oreochromis mossambicus. Aggressive Behay. 22: 37–45.CrossRefGoogle Scholar
  31. a, B.L., M.W. Davis & C.H. Ryer. 1994. Behavioural defects in hatchery-reared fish: potential effects on survival following release. Aquacult. Fish. Manag. 25: 19–34.Google Scholar
  32. Pitcher, T.J. 1983. Heuristic definitions of shoaling behaviour. Animal Behay. 31: 611–613.CrossRefGoogle Scholar
  33. Pitcher, T.J. & J.K. Parrish. 1993. Functions of shoaling behaviour in teleosts. pp. 363–439. In: T.J. Pitcher (ed.) Behaviour of Teleost Fishes, Chapman & Hall, London.CrossRefGoogle Scholar
  34. Pitcher, T.J., C.J. Wyche & A.E. Magurran. 1982. Evidence for position preferences in schooling mackerel. Anim. Behay. 30: 932–934.CrossRefGoogle Scholar
  35. Polis, G.A. 1981. The evolution and dynamics of intraspecific predation. Ann. Rev. Ecol. Syst. 12: 225–251.CrossRefGoogle Scholar
  36. Potthoff, T. 1984. Clearing and staining techniques. pp. 35–37. In: H.G. Moser, W.J. Richards, D.M. Cohen, M.P. Fahay, A.W.J. Kendall & S.L. Richardson (ed.) Potthoff, T. 1, Lawrence.Google Scholar
  37. Ruzzante, D.E. 1994. Domestication effects on aggressive and schooling behavior in fish. Aquaculture 120: 1–24.CrossRefGoogle Scholar
  38. Safran, P. 1990. Drifting seaweed and associated ichthyofauna: floating nursery in the Tohoku waters. La mer 28: 225–239.Google Scholar
  39. Sakakura, Y., M. Tagawa & K. Tsukamoto 1998a. Whole-body cortisol concentrations and ontogeny of aggressive behavior in yellowtail (Seriola quinqueradiata Temminck & Schlegel; Carangidae). Gen. Comp. Endocrinol. 109: 286–292.Google Scholar
  40. Sakakura, Y., S. Koshio, Y. Lida, K. Tsukamoto, T. Kida & J.H. Blom. 1998b. Dietary vitamin C improves the quality of yellowtail, Seriola quinqueradiata, seedlings. Aquaculture 161: 427–436.CrossRefGoogle Scholar
  41. Sakakura, Y. & K. Tsukamoto. 1996. Onset and development of cannibalistic behaviour in early life stage of yellowtail. J. Fish Biol. 48: 16–29.CrossRefGoogle Scholar
  42. Sakakura, Y. & K. Tsukamoto. 1997a. Age composition in the schools of juvenile yellowtail, Seriola quinqueradiata, associated with drifting seaweeds in the East China Sea. Fish. Sci. 63: 37–41.Google Scholar
  43. Sakakura, Y. & K. Tsukamoto. 1997b. Effects of water temperature and light intensity on the aggressive behavior in the juvenile yellowtails. Fish. Sci. 63: 42–45.Google Scholar
  44. Sakakura, Y. & K. Tsukamoto. 1998a. Social ranks in schools of juvenile yellowtail, Seriola quinqueradiata. J. Appl. Ichthyol. 14: 69–73.CrossRefGoogle Scholar
  45. Sakakura, Y. & K. Tsukamoto. 19986. Effects of density, starvation and size difference on aggressive behaviour in juvenile yellowtails (Seriola quinqueradiata). J. Appl. Ichthyol. 14: 9–13.Google Scholar
  46. Schjelderup-Ebbe, T. 1935. Social behavior of birds. pp. 947–972. In: T. Murchison (ed.) Handbook of Social Psychology, Clark University Press, Worcester.Google Scholar
  47. Shaw, E. 1962. The schooling of fishes. Scient. Amer. 206: 128–138.CrossRefGoogle Scholar
  48. Shaw, E. 1978. Schooling fishes. Amer. Scient. 66: 166–175.Google Scholar
  49. Sokal, R.R. & F.J. Rohlf. 1995. Analysis of frequencies. pp. 685–793. In: R.R. Sokal & F.J. Rohlf (ed.) Biometry, W.H. Freeman and Company, New York.Google Scholar
  50. Svâsand, T. 1993. Are reared juveniles suited for release? ICES Council Meeting F34: 1–13 (mimeogr.).Google Scholar
  51. Tagawa, M. & T. Hirano. 1989. Changes in tissue and blood concentrations of thyroid hormones in developing chum salmon. Gen. Comp. Endocrinol. 76: 437–443.PubMedCrossRefGoogle Scholar
  52. Tanaka, M., J.B. Tanagonan, M. Tagawa, E.G.D. Jesus, H. Nishida, M. Isaka, R. Kimura & T. Hirano. 1995. Development of the pituitary, thyroid and interrenal glands and applications of endocrinology to the improved rearing of marine fish larvae. Aquaculture 135: 111–126.CrossRefGoogle Scholar
  53. Tsukamoto, K. 1985. Mass-marking of ayu eggs and larvae by tetracycline-tagging of otoliths. Bull. Japan. Soc. Sci. Fish. 51: 903–911.CrossRefGoogle Scholar
  54. Tsukamoto, K. 1988. Migratory mechanisms and behavioral characteristics in ayu. pp. 100–133. In: T. Ueno & M. Okiyama (ed.) Ichthyology Currents, Asakura Shoten, Tokyo (in Japanese).Google Scholar
  55. Tsukamoto, K., Y. Seki, T. Oba, M. Oya & M. Iwahashi. 1989. Application of otolith to migration study of salmonids. Physiol. Ecol. Japan. 1: 119–140.Google Scholar
  56. Tsukamoto, K. & K. Uchida. 1992. Migration mechanism of the ayu. pp. 145–172. In: V.I. Ilyichev, V.V. Anikiev (ed.) Oceanic and Anthropogenic Controls of Life in the Pacific Ocean, Kluwer Academic Publishers, Dordrect.CrossRefGoogle Scholar
  57. Uchida, K., Y. Dotu, S. Mito & K. Nakahara. 1958. The spawning and early life history of `burl’, Japanese yellow tail, Seriola quinqueradiata Temminck et Schlegel. Sci. Bull. Fac. Agr., Kyushu Univ. 16: 329–342.Google Scholar
  58. Umeda, S. & A. Ochiai. 1973. On the development of the structure and function of the alimentary tract of the yellowtail from the larval to the juvenile stage. Bull. Japan. Soc. Sci. Fish. 39: 923–930.CrossRefGoogle Scholar
  59. Watanabe, T. & V. Kiron. 1994. Prospects in larval fish dietetics. Aquaculture 124: 223–251.CrossRefGoogle Scholar
  60. Yamagishi, H. 1962. Growth relation in some small experimental populations of rainbow trout with special reference to social relations among individuals. Japan. J. Ecol. 12: 13–53.Google Scholar

Copyright information

© Springer Science+Business Media Dordrecht 1998

Authors and Affiliations

  • Yoshitaka Sakakura
    • 1
  • Katsumi Tsukamoto
    • 1
  1. 1.Division of Fisheries Ecology, Ocean Research InstituteThe University of TokyoNakano, Tokyo 164Japan

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