Marine Biology

, Volume 61, Issue 1, pp 27–40

Patterns of growth, energy utilization and reproduction in some meso- and bathypelagic fishes off Southern California

  • J. J. Childress
  • S. M. Taylor
  • G. M. Cailliet
  • M. H. Price
Article

Abstract

We have studied growth, energy use and reproduction in 4 mesopelagic fishes and 5 bathypelagic fishes living off Southern California (USA). All of the mesopelagic species underwent diurnal vertical migrations, while none of the bathypelagic species did so. The life histories of these pelagic fishes were compared among themselves and with epipelagic sardines and anchovies studied by others. The epipelagic species had the highest growth rates (estimated from otoliths, expressed in standard length or kilocalories), the mesopelagic species had the lowest growth rates and the bathypelagic species had intermediate growth rates. The relatively rapid growth rates of the bathypelagic fishes were achieved by high relative growth efficiencies made possible by low metabolic rates. Of the species studied, the lifespans of the epipelagic and bathypelagic species ranged from 4 to 8 yr and the lifespans of mesopelagic species from 5 to 8 yr. Data on egg diameters suggest that the mesopelagic species first reproduce in their 3rd yr, while the bathypelagic species do so in their last year. Epipelagic fishes generally have a large size, rapid growth, long life and early, repeated reproduction. Mesopelagic fishes are characterized by small size, slow growth, long life and early, repeated reproduction. Bathypelagic fishes generally have large size, rapid growth, somewhat shorter lives and late reproduction, which is possible a single event. The latter pattern is evidently feasible only in a rather stable environment where juvenile survivorship would always display relatively low variability. Many unusual characteristics of deep-living animals have possibly been selected by factors peculiar to the environment; however, such characteristics are just as likely to have been selected by factors equally present in many other environments, but not expressed there due to masking selective forces. In particular, we have in mind the darkness, stability and homogeneity of the bathypelagic realm as phenomena which represent the effective absence of many selective forces.

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Literature Cited

  1. Barham, E. G.: Deep-sea fishes' lethargy and vertical orientation. In: Proceedings of an international symposium on biological sound scattering in the ocean, pp 100–118. Ed. by G. B. Farquhar. Washington, D. C.: Maury Center for Ocean Sciences. Department of the Navy 1971Google Scholar
  2. Blackburn, M. B.: Regressions between biological oceanographic measurements in the eastern tropical Pacific and their significance to ecological efficiency. Limnol. Oceanogr. 18, 552–563 (1973)Google Scholar
  3. Blackburn, M. B.: Studies on pelagic animal biomasses. In: Oceanic sound scattering prediction, pp 283–291. Ed. by N. R. Anderson and B. J. Zahuranec. New York: Plenum Press 1977Google Scholar
  4. Blackburn, M. B., R. M. Laurs, R. W. Owen and B. Zeitschel: Seasonal and areal changes in standing stocks of phytoplankton, zooplankton and micronekton in the eastern tropical Pacific. Mar. Biol. 7, 14–31 (1970)Google Scholar
  5. Brett, J. R. and T. D. D. Groves: Physiological energetics. In: Fish physiology, Vol. VIII. pp 279–351. Ed. by W. S. Hoar and D. J. Randall. New York: Academic Press 1979Google Scholar
  6. Brown, D. W.: Hydrography and midwater fishes of three contigous oceanic areas off Santa Barbara, California. Publs Los Ang. Mus. 261, 1–30 (1974)Google Scholar
  7. Childress, J. J.: The respiratory physiology of the oxygen minimum layer mysid Gnathophausia ingens, 142 pp. Ph.D. dissertation, Stanford University 1969Google Scholar
  8. Childress, J. J.: Respiratory rate and depth of occurrence of midwater animals. Limnol. Oceanogr. 16, 104–106 (1971)Google Scholar
  9. Childress, J. J.: The respiratory rates of midwater crustaceans as a function of depth of occurrence and relation to the oxygen minimum layer off Southern California. Comp. Biochem. Physiol. 50A, 787–799 (1975)Google Scholar
  10. Childress, J. J. and T. J. Mickel: A motion compensated shipboard precision balance system. Deep-Sea Res. (In press) (1980)Google Scholar
  11. Childress, J. J. and M. H. Nygaard: The chemical composition of midwater fishes as a function of depth of occurrence off Southern California. Deep-Sea Res. 10, 1093–1109 (1973)Google Scholar
  12. Childress, J. J. and M. Nygaard: Chemical composition and buoyancy of midwater crustaceans as a function of depth of occurrence off Southern California. Mar. Biol. 27, 225–238 (1974)Google Scholar
  13. Childress, J. J. and M. H. Price: Growth rate of the bathypelagic crustacean Gnathophausia ingens (Mysidacea: Lophogastridae). I. Dimensional growth and population structure. Mar. Biol. 50, 47–62 (1978)Google Scholar
  14. Childress, J. J. and G. N. Somero: Depth-related enzymic activities in muscle, brain and heart of deep-living pelagic marine teleosts. Mar. Biol. 52, 273–283 (1979)Google Scholar
  15. Clarke, T. A.: Some aspects of the ecology of lanternfishes in the Pacific Ocean near Hawaii. Fish. Bull. U.S. 71, 401–434 (1973)Google Scholar
  16. Clarke, T. A.: Some aspects of the ecology of stomiatoid fishes in the Pacific Ocean near Hawaii. Fish. Bull. U.S. 22, 337–351 (1974)Google Scholar
  17. Clarke, T. A.: Diel feeding patterns of 16 species of mesopelagic fishes from Hawaiian waters. Fish. Bull. U.S. 76, 495–513 (1978)Google Scholar
  18. Clarke, T. A. and P. J. Wagner: Vertical distribution and other aspects of the ecology of certain mesopelagic fishes taken near Hawaii. Fish. Bull U.S. 74, 635–645 (1976)Google Scholar
  19. Cole, L. J.: The population consequences of life history phenomena. Q. Rev. Biol. 29, 103–139 (1954)Google Scholar
  20. Collins, R. A. and J. D. Spratt: Age determination of Northern anchovies Engraulis mordax, from otoliths. In: The Northern anchovy (Engraulis mordax) and its fishery 1965–1968, pp 39–55. Ed. by J. D. Messersmith. Sacramento: California Department of Fish and Game 1969. (Calif. Fish Game Fish Bull. No. 147)Google Scholar
  21. Enright, J. T.: Diurnal vertical migration: adaptive significance and timing. Part I. Selective advantage: a metabolic model. Limnol. Oceanogr. 22, 856–872 (1977)Google Scholar
  22. Fast, T. N.: Some aspects of the natural history of Stenobrachius leucopsaurus (Eigenmann and Eigenmann), 107 pp. Ph.D. thesis, Stanford University, Stanford 1960Google Scholar
  23. Fitch, J. E. and R. J. Lavenberg: Deep water teleostean fishes of California, 155 pp. Berkeley and Los Angeles: University of California Press 1968Google Scholar
  24. Grassle, J. F. and H. L. Sanders: Life histories and the role of disturbance. Deep-Sea Res. 20, 643–659 (1973)Google Scholar
  25. Halliday, R. G.: Growth and vertical distribution of the glacier lanternfish, Benthosema glacial, in the northwestern Atlantic. J. Fish. Res. Bd Can. 27, 105–116 (1970)Google Scholar
  26. Hirschfield, M. F. and D. W. Tinkle: Natural selection and the evolution of reproductive effort. Proc. natn. Acad. Sci U.S.A. 72, 2227–2231 (1975)Google Scholar
  27. Iles, T. D.: The tactics and strategy of growth in fishes. In: Sea fisheries research, pp 331–345. Ed. by F. R. Harden Jones. New York: John Wiley & Sons 1974Google Scholar
  28. Jannasch, H. W., K. Eimhjillen, C. O. Wirsen and A. Farmanfarmian: Microbial degradation of organic matter in the deep sea. Science, N.Y. 171, 672–675 (1971)Google Scholar
  29. Jannasch, H. W. and C. O. Wirsen: Deep-sea microorganisms: in situ response to nutrient enrichment. Science, N.Y. 180, 641–643 (1973)Google Scholar
  30. Karnella, C. and R. H. Gibbs, Jr.: The lanternfish Lobiancha dofleini: an example of life-history information in prediction of oceanic sound scattering. In: Oceanic sound scattering prediction, pp 361–379. Ed. by N. R. Anderson and B. J. Zahuranec. New York: Plenum Press 1977Google Scholar
  31. Lasker, R.: Utilization of zooplankton energy by a Pacific sardine population in the California current. In: Marine food chains, pp 265–284. Ed. by J. H. Steele. Edinburgh: Oliver & Boyd 1970Google Scholar
  32. Legand, M.: Seasonal variations in the Indian Ocean along 110°E. VI. Macroplankton and micronekton biomass. Aust. J. mar. Freshwat. Res. 20, 85–103 (1969)Google Scholar
  33. Legand, M., P. Bourret, R. Grandperrin and J. Rivaton: A preliminary study of some micronektonic fishes in the equatorial and tropical western Pacific. In: Scientific exploration of the south Pacific, pp 226–235. Ed. by W. S. Wooster. Washington, D.C.: National Academy of Sciences 1970Google Scholar
  34. Lewontin, R. C.: Selection for colonizing ability. In: The genetics of colonizing species, pp 77–91. Ed. by H. G. Baker and G. Ledyard Stebbins. New York: Academic Press 1965Google Scholar
  35. Mauchline, J.: The biology of bathypelagic organisms, especially Crustacea. Deep-Sea Res. 19, 753–780 (1972)Google Scholar
  36. Mauchline, J.: Estimating production of midwater organisms. In: Oceanic sound scattering prediction, pp 117–215. Ed. by N. R. Anderson and B. J. Zahuranec. New York: Plenum Press 1977Google Scholar
  37. McLaren, I. A.: Effects of temperature on growth of zooplankton and the adaptive value of vertical migration. J. Fish. Res. Bd Can. 20, 685–727 (1963)Google Scholar
  38. Meats, A.: The relative importance to population increase of fluctuations in mortality, fecundity and the time variables of the reproductive schedule. Oecologia (Berl.) 6, 223–237 (1971)Google Scholar
  39. Mertz, D. B.: Life history phenomena in increasing and decreasing populations. In: Statistical ecology Vol. II. Sampling and modeling biological populations and population dynamics, pp 361–399. Ed. by G. P. Patel, E. C. Pielou, and W. E. Waters. University Park: Pennsylvania State University Press 1971Google Scholar
  40. Murphy, G. J.: Pattern in life history and the environment. Am. Nat. 102, 390–404 (1968)Google Scholar
  41. Nikolsky, G. V.: The ecology of fishes, [Transl. from Russian by L. Birkett] 352 pp. London: Academic Press 1963Google Scholar
  42. Panella, G.: Otolith growth patterns: an aid in age determination in temperate and tropical fishes. In: Ageing of fish, pp 28–39. Ed. by T. E. Bagenel. Old Woking: Unwin Bros. 1974Google Scholar
  43. Pearcy, W. G.: Some distributional features of mesopelagic fishes off Oregon. Deep-Sea Res. 13, 153–165 (1970)Google Scholar
  44. Reid, J. L.: Some thoughts on the dependence of sound speed and the scattering layers upon ocean circulation. In: Oceanic sound scattering prediction, pp 15–64. Ed. by N. R. Anderson and B. J. Zahuranec. New York: Plenum Press 1977Google Scholar
  45. Robertson, D. A.: Planktonic eggs of the lanternfish, Lampanyctodes hectoris (family Myctophidae). Deep-Sea Res. 24, 849–852 (1977)Google Scholar
  46. Rowe, G. T., P. T. Polloni and S. G. Horner: Benthic biomass estimates from the northwestem Atlantic Ocean and the northern Gulf of Mexico. Deep-Sea Res. 21, 641–650 (1974)Google Scholar
  47. Smith, K. L.: Metabolism of abyssopelagic fishes: in situ measurements of the rattail, Coryphaenoides armatus. Nature, Lond. 274, 362–364 (1978)Google Scholar
  48. Smith, K. L., Jr. and R. R. Hessler: Respiration of benthopelagic fishes: in situ measurements at 1230 meters. Science, N.Y. 184, 72–73 (1974)Google Scholar
  49. Smith, K. L., Jr. and J. M. Teal: Deep-sea benthic community respiration: an in situ study at 1850 meters. Science, N.Y. 179, 282–283 (1973)Google Scholar
  50. Smoker, W. and W. G. Pearcy: Growth and reproduction of the lanternfish Stenobrachius leucopsaurus. J. Fish. Res. Bd Can. 27, 1265–1275 (1970)Google Scholar
  51. Somero, G. N. and J. J. Childress: A violation of the metabolism-size scaling paradigm: activities of glycolytic enzymes in muscle increase in larger size fishes. Physiol. Zoöl. 53, 322–337 (1980)Google Scholar
  52. Torres, J. J., B. W. Belman and J. J. Childress: Oxygen consumption rates of midwater fishes off California. Deep-Sea Res. 26A, 185–197 (1979)Google Scholar
  53. Tranter, D. J.: Seasonal studies of a pelagic ecosystem (meridian 110°E). In: The biology of the Indian Ocean, pp 487–520. Ed. by B. Zeitzchel. New York: Springer-Verlag 1973Google Scholar
  54. Turekian, K. K., J. K. Cochran, D. D. Kharkar, R. M. Cerrato, J. R. Vaisnys, H. L. Sanders, J. F. Grassle and J. A. Allen: Slow growth rate of a deep-sea clam determined by 228Ra chronology. Proc. natn. Acad. Sci (U.S.A.) 72, 2829–2832 (1975)Google Scholar
  55. Vinogradov, M. E.: Vertical distribution of the oceanic zooplankton, 339 pp. Moskva: Izdatel stvo “Nauka” 1968 [Transl. by Israel Program for Scientific Translation, U.S. Department of Commerce, Clearinghouse for Federal Scientific and Technical Information, Springfield, Va. 2215, USA, 1970]Google Scholar
  56. Warner, R. R.: The coevolution of behavioral and life history characteristics. In: Sociobiology: beyond nature-nurture? Ed. by G. W. Barlow and J. Silverberg. Boulder, Colorado: Westview Press (In press)Google Scholar
  57. Wirsen, C. O. and H. W. Jannasch: Decomposition of solid organic materials in the deep sea. Envir. Sci. Technol. 10, 880–886 (1976)Google Scholar

Copyright information

© Springer-Verlag 1980

Authors and Affiliations

  • J. J. Childress
    • 1
    • 2
  • S. M. Taylor
    • 3
    • 4
  • G. M. Cailliet
    • 5
  • M. H. Price
    • 1
    • 2
  1. 1.Occanic Biology Group, Marine Science InstituteUniversity of California at Santa BarbaraSanta BarbaraUSA
  2. 2.Department of Biological SciencesUniversity of California at Santa BarbaraSanta BarbaraUSA
  3. 3.Lawrence Hall of ScienceUniversity of California at BerkeleyBerkeleyUSA
  4. 4.Group in Science and Mathematics EducationUniversity of California at BerkeleyBerkeleyUSA
  5. 5.Moss Landing Marine LaboratoriesMoss LandingUSA

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