Skip to main content
Log in

Seasonal breeding aggregations in low-density populations of the bathyal echinoid Stylocidaris lineata

  • Published:
Marine Biology Aims and scope Submit manuscript

Abstract

Reproduction of bathyal cidaroid sea urchins was studied between 1985 and 1991 with the aid of a manned submersible in the northern Bahamas. During May 1988 and February 1990, discrete, single-species aggregations of Stylocidaris lineata containing 2 to 6 individuals were observed between 510 and 640 m depths. Reproductive conditions of isolated and aggregated individuals were determined histologically. In February, all individuals, regardless of their spatial distribution, contained developing gametes. During the May spawning season, most isolated individuals contained spent gonads with only relict gametes, whereas individuals in discrete aggregations mostly contained ripe gonads with mature or nearly-mature gametes. Aggregations were not observed during the autumn months, when gonads were spent or immature. These data suggest that bathyal cidaroids aggregate for reproduction. An in situ survey during May indicated that pairs of S. lineata are more common than larger clumps, but no more so than predicted by chance. Homosexual and heterosexual pairs occur at the relative frequencies predicted on the basis of sex ratio. We evaluated the need for reproductive aggregation by applying Denny's (1988) model that predicts downstream sperm concentration in a turbulent boundary layer. Flow parameters were measured with dye injected from the submersible, sperm-release rate was estimated in the laboratory, and the relationship between fertilization success and sperm concentration was determined in a laboratory dilution-experiment. The model predicted that, on smooth sandy bottoms at bathyal depths, sperm concentration should remain high enough to fertilize at least some eggs several meters directly downstream from a spawning male. Aggregation may facilitate spawning synchrony, increase gamete encounter probabilities, or cause gametes to be retained at high concentrations near the adults long enough for fertilization to occur.

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

  • Beach, D. H., Hanscomb, N. J., Ormond, R. F. G. (1975). Spawning pheromone in crown-of-thorns starfish. Nature, Lond. 254: 135–136

    Google Scholar 

  • Billett, D. S. M., Hansen, B. (1982). Abyssal aggregations of Kolga hyalina (Echinodermata: Holothuroidea) in the north-east Atlantic Ocean: a preliminary report. Deep-Sea Res. 29: 799–818

    Google Scholar 

  • Boschma, H. (1924). Über einen Fall von Kopulation bei einer Asteridae (Archaster typicus). Zool. Anz. 58: 283–285

    Google Scholar 

  • Cohn, E. J. (1918). Studies in the physiology of spermatozoa. Biol. Bull. mar. biol. Lab., Woods Hole 34: 167–218

    Google Scholar 

  • Denny, M. W. (1988). Biology and the mechanics of the wave-swept environment. Princeton University Press, Princeton

    Google Scholar 

  • Denny, M. W., Shibata, M. F. (1989). Consequences of surf-zone turbulence for settlement and external fertilization. Am. Nat. 134: 859–889

    Google Scholar 

  • Dix, T. G. (1969). Aggregating in the echinoid Evechinus chloroticus. Pacif. Sci. 23: 123–124

    Google Scholar 

  • Eckelbarger, K. J., Young, C. M., Cameron, J. L. (1989a). Modified sperm in echinoderms from the bathyal and abyssal zones of the deep sea. In: Ryland, J.S. & Tyler, P. A. (eds). Reproduction, genetics and distributions of marine organisms. Olsen & Olsen, Fredensborg, Denmark, p. 67–74

    Google Scholar 

  • Eckelbarger, K. J., Young, C. M., Cameron, J.L. (1989b). Modified sperm ultrastructure in four species of soft-bodied echinoids (Echinodermata: Echinothurridae) from the bathyal zone of the deep sea. Biol. Bull. mar. biol. Lab., Woods Hole 177: 230–236

    Google Scholar 

  • Eckelbarger, K. J., Young, C. M., Cameron, J. L. (1989c). Ultrastructure and development of dimorphic sperm in the abyssal echinoid Phrissocystis multispina (Echinodermata: Echinoidea): implications for deep-sea reproductive biology. Biol. Bull. mar. biol. Lab., Woods Hole 176: 257–271

    Google Scholar 

  • Fujioti, K., Taira, A., Kobayeshi, K., Nakamura, K., Iiyama, T., Cadet, J.-P., Lallemand, S., Girard, D. (eds.) (1987) 6000 m deep: a trip to the Japanese trenches. University of Tokyo Press, Tokyo

    Google Scholar 

  • Gemmill, J. F. (1900). On the vitality of ova and spermatozoa of certain animals. J. Anat. Physiol., Paris 34: 163–181

    Google Scholar 

  • Giese, A. C., Kanatani, H. (1987). Maturation and spawning. In: Giese, A. C., Pearse, J. S., Pearse, V. B. (eds.) Reproduction of marine invertebrates. Vol. 9. General aspects: seeking unity in diversity. Blackwell, Palo Alto and Boxwood, Pacific Grove

    Google Scholar 

  • Gilmore, R. G., Hastings, P. A., Kulczycki, G. R., Jennison, B. L. (1981). Crystalline rotenone as a selective fish toxin. Fla Scient. 44: 193–203

    Google Scholar 

  • Grant, A., Tyler, P. A. (1983). The analysis of data in studies of invertebrate reproduction. I. Introduction and statistical analysis of gonad indices and maturity indices. Int. J. Invert. Reprod. 6: 259–269 (1983)

    Google Scholar 

  • Grassle, J. F., Sanders, H. L., Hessler, R. R., Rowe, G. T., McLellan, T. (1975). Pattern and zonation: a study of the bathyal megafauna using the research submersible Alvin. Deep-Sea Res. 22: 457–481

    Google Scholar 

  • Komatsu, M. (1983). Development of the sea star, Archaster typicus, with a note on male-on-female superposition. Annotnes zool, jap. 56: 187–195

    Google Scholar 

  • Levitan, D. R. (1991). Influence of body size and population density on fertilization success and reproductive output in a free-spawning invertebrate. Biol. Bull. mar. biol. Lab., Woods Hole 181: 261–268

    Google Scholar 

  • Lillie, F. R. (1915). Studies of fertilization. VII. Analysis of variations in the fertilization power of sperm suspensions of Arbacia. Biol. Bull. mar. biol. Lab., Woods Hole 28: 229–251

    Google Scholar 

  • McEuen, F. S. (1988). Spawning behaviors of northeast Pacific sea cucumbers (Holothuroidea: Echinodermata). Mar. Biol. 98: 565–585

    Google Scholar 

  • Miller, R. L. (1989). Evidence for the presence of sexual pheromones in free-spawning starfish. J exp. mar. Biol. Ecol. 130: 205–221

    Google Scholar 

  • Mortensen, T. (1931). Contributions to the study of the development and larval forms of echinoderms I–II. K. danske Vidensk. Selsk. Skr. (Naturvid. Math. Afd. 9 raekke) 4: 1–39

    Google Scholar 

  • Orton, J. H. (1914). On the breeding habits of Echinus miliaris, with a note on the feeding habits of Patella vulgata. J. mar. biol. Ass. U.K. 10: 254–257

    Google Scholar 

  • Pawson, D. L. (1976). Some aspects of the biology of deep-sea echinoderms. Thalassia jugosl. 12: 287–293

    Google Scholar 

  • Pearse, J. S., McClary, D. J., Sewell, M. A., Austin, W. C., Prez-Ruzafa, A., Byrne, M. (1988). Simultaneous spawning of six species of echinoderms in Barkley Sound, British Columbia. Invert. Reprod. Dev. 14: 279–288

    Google Scholar 

  • Pennington, J. T. (1985). The ecology of fertilization of echinoid eggs: the consequences of sperm dilution, adult aggregation, and synchronous spawning. Biol. Bull. mar. biol. Lab., Woods Hole 169: 417–430

    Google Scholar 

  • Pielou, E. C. (1977). Mathematical ecology. John Wiley & Sons, New York

    Google Scholar 

  • Rice, A. L., Alred, R. G., Darlington, E., Wild, R. A. (1982). The quantitative estimation of the deep-sea megabenthos: a new approach to an old problem. Oceanol. Acta 5: 63–72

    Google Scholar 

  • Run, J-Q, Chen, C.-P., Chang, K.-H., Chia, F.-S. (1988). Mating behaviour and reproductive cycle of Archaster typicus (Echinodermata: Asteroidea). Mar. Biol. 99: 247–253

    Google Scholar 

  • Sokal, R. R., Rohlf, F. J. (1981). Biometry. The principles and practice of statistics in biological research. 2nd ed. W. H. Freeman & Co., New York

    Google Scholar 

  • Starr, M., Himmelman, J. H., Therriault, J. (1990). Direct coupling of marine invertebrate spawning with phytoplankton blooms. Science, N.Y. 247: 1071–1074

    Google Scholar 

  • Thorson, G. (1950). Reproductive and larval biology of marine bottom invertebrates. Biol. Rev. 25: 1–45

    Google Scholar 

  • Tyler, A., Monroy, A., Metz, C. B. (1956). Fertilization of fertilized sea urchin eggs. Biol. Bull. mar. biol. Lab., Woods Hole 110: 184–195

    Google Scholar 

  • Tyler, P. A. (1988). Seasonality in the deep sea. Oceanogr. mar. Biol. A. Rev. 26: 227–258

    Google Scholar 

  • Tyler, P. A., Billett, D. S. M., Young, C. M., Giles, L. A. (1992). Reproductive biology and behaviour in the deep-sea holothurian genus Paroriza (Holothuroidea: Synallactidae). J. mar. Biol. Ass. U.K. 72: 447–462

    Google Scholar 

  • Vogel, H., Czihak, G., Chang, P., Wolf, W., (1982). Fertilization kinetics of sea urchin eggs. Mathl Biosci. 58: 189–216

    Google Scholar 

  • Wimbush, M. (1976). The physics of the benthic houndary layer. In: McCare, I. N. (ed.) The benthic boundary layer. Plenum Press, New York, p. 3–10

    Google Scholar 

  • Wimbush, M., Munk, W. (1970). The benthic boundary layer. In: Maxwell, A. E. (ed.) The sea. Wiley-Interscience, New York, p. 731–758

    Google Scholar 

  • Yoshida, M. (1952). Some observations on the maturation of the sea urchin, Diadema setosum. Annotnes zool. jap. 25: 265–271

    Google Scholar 

  • Yund, P. O. (1990). An in situ measurement of sperm dispersal in a colonial marine hydroid. J. exp. Zool. 253: 102–106

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Young, C.M., Tyler, P.A., Cameron, J.L. et al. Seasonal breeding aggregations in low-density populations of the bathyal echinoid Stylocidaris lineata . Marine Biology 113, 603–612 (1992). https://doi.org/10.1007/BF00349704

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00349704

Keywords

Navigation