Skip to main content
Log in

Intraspecific variation in Gape–prey size Relationships and Feeding Success During Early Ontogeny in Red Drum, Sciaenops Ocellatus

  • Published:
Environmental Biology of Fishes Aims and scope Submit manuscript

Abstract

The relationship between predator gape and prey consumption in laboratory-reared larva and field-caught early juvenile red drum, Sciaenops ocellatus, was investigated in light of the hypothesis that feeding success varies throughout the early life history intervals of marine fishes. We expected the feeding ability of red drum to be more strongly constrained by mouth gape in smaller fish and expected this ability to improve with gape size. To test this hypothesis, field-caught, early juvenile red drum were examined to determine the relationship between gape size and prey size consumed. In field-caught early juveniles, gape (height and width) and prey size consumed (length and width) increased linearly with standard length (SL); however, mean width of prey consumed was only 20–47% of gape width. Furthermore, when regressed on SL, gape width yielded a higher slope than prey width. To further test this hypothesis on less developed, pre-metamorphic fish, age-specific differences in gape, number of prey and size of prey consumed prior to metamorphosis were determined from laboratory-reared red drum larvae. Similar patterns were observed for gape height– and gape width–SL relationships in laboratory-reared red drum larvae. Size of consumed prey increased from three days from hatching (dfh) to 18 dfh. The percentage of feeding larvae also increased from ∼3% at 3 dfh to 97% at 18 dfh. In both field-caught, early juvenile red drum and laboratory-reared larvae, there was little evidence that the size of prey consumed was constrained by mouth gape. It is hypothesized that besides gape size, the development of other features of the feeding mechanism (e.g., hyoid and opercular series) influences prey-capture performance prior to settlement in marine fishes.

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.

Institutional subscriptions

Similar content being viewed by others

References cited

  • Ahlstrom, E.H, J.L. Butler & B.Y. Sumida. 1976. Pelagic stromateoid fishes (Pisces, Perciformes) of the eastern Pacific: Kinds, distributions, and early life histories and observations on five of these from the northwest Atlantic. Bull. Mar. Sci. 26: 285-402.

    Google Scholar 

  • Arthur, D.K. 1976. Food and feeding of larvae of three fishes occurring in the California current (Sardinops sagax), (Engraulis mordax) and (Trachurus symmetricus). U.S. Fish. Bull. 74: 517-530.

    Google Scholar 

  • Balon, E.K. 1975. Terminology of intervals in fish development. J. Fish. Res. Board Can. 32: 1663-1670.

    Google Scholar 

  • Balon, E.K. 1984. Reflections on some decisive events in the early life of fishes. Trans. Amer. Fish. Soc. 113: 178-185.

    Google Scholar 

  • Blaxter, J.H.S. & M.E. Staines. 1971. Food searching potential in marine fish larvae. pp. 467-485. In: D.J. Crisp (ed.) Proceedings of the 4th European Marine Biology Symposium, Cambridge University Press, Cambridge.

    Google Scholar 

  • Bremigan, M.T. & R.A. Stein. 1994. Gape-dependent larval foraging and zooplankton size: Implications for fish recruitment across systems. Can. J. Fish. Aquat. Sci. 51: 913-922.

    Google Scholar 

  • Canino, M.F. & K.M. Bailey. 1995. Gut evacuation of walleye pollock larvae in response to feeding conditions. J. Fish Biol. 46: 389-403.

    Google Scholar 

  • Connel, S.D. & G.P. Jones. 1991. The influence of habitat complexity on postrecruitment processes in a temperate reef fish population. J. Exp. Mar. Biol. Ecol. 151: 271-294.

    Google Scholar 

  • Coughlin, D.J. 1991. Ontogeny of feeding behavior in firstfeeding Atlantic salmon (Salmo salar). Can. J. Fish. Aquat. Sci. 48: 1896-1904.

    Google Scholar 

  • Cushing, D.H. 1981. Fisheries Biology, a Study in Population Dynamics. University of Wisconsin Press, Madison. 295 pp.

    Google Scholar 

  • DeVries, D.R., M.T. Bremigan & R.A. Stein. 1998. Prey selection by larval fishes as influenced by available zooplankton and gape limitation. Trans. Amer. Fish. Soc. 127: 1040-1050.

    Google Scholar 

  • Doi, M., A. Ohno, H. Kohno, Y. Taki & T. Singhagraiwan. 1997. Development of feeding ability in red snapper (Lutjanus argentimaculatus) early larvae. Fish. Sci. 63: 845-853.

    Google Scholar 

  • Flores-Coto, C., A. Sanchez-Iturbe, F. Zavala-Garcia & S.M. Warlen. 1998. Age, growth, mortality and food habits of larval (Stellifer lanceolatus), (Cynoscion arenarius) and (Cynoscion nothus) (Pisces: Sciaenidae) from the southern Gulf of Mexico. Estuar. Coast. Shelf Sci. 47: 593-602.

    Google Scholar 

  • Fowler, J., L. Cohen & P. Jarvis. 1998. Practical Statistics for Field Biology. John Wiley & Sons, New York. 259 pp.

    Google Scholar 

  • Govoni, J.J., P.B. Ortner, F. Al-Yamani & L.C. Hill. 1986. Selective feeding of spot (Leiostomus xanthurus) and Atlantic croaker (Micropogonius undulatus) larvae in the northern Gulf of Mexico. Mar. Ecol. Prog. Ser. 28: 175-183.

    Google Scholar 

  • Grubich, J.R. 2000. Crushing motor patterns in drum (Teleostei: Sciaenidae): Functional novelties associated with molluscivory. J. Exp. Biol. 203: 3161-3176.

    Google Scholar 

  • Hagen, N. 1993. Effect of different prey and larval densities on the gut content of plaice (Pleuronectes platessa L.) at initial feeding. pp. 180-182. In: B.T. Walther & H.J. Fyhn (ed.) Physiological and Biochemical Aspects of Fish Development, University of Bergen, Norway.

    Google Scholar 

  • Hansen, M.J. & D.H. Wahl. 1981. Selection of small Daphnia pulex by yellow perch fry in Oneida Lake, New York. Trans. Amer. Fish. Soc. 110: 64-71.

    Google Scholar 

  • Holt, G.J. & S.A. Holt. 2000. Vertical distribution and the role of physical processes in the feeding dynamics of two larval sciaenids (Sciaenops ocellatus) and (Cynoscion nebulosus). Mar. Ecol. Prog. Ser. 193: 181-190.

    Google Scholar 

  • Holt, G.J., A.G. Johnson, C.R. Arnold, W.A. Fable, Jr. & T.D. Williams. 1981. Description of eggs and larvae of laboratory reared red drum (Sciaenops ocellata). Copeia 1981: 751-756.

    Google Scholar 

  • Houde, E.D. 1978. Critical food concentrations for larvae of three subtropical marine fishes. Bull. Mar. Sci. 28: 395-411.

    Google Scholar 

  • Houde, E.D. & R.C. Schekter. 1980. Feeding by marine fish larvae: Developmental and functional responses. Env. Biol. Fish. 5: 315-334.

    Google Scholar 

  • Hunt von Herbing, I., T. Miyake, B.K. Hall & R.G. Boutilier. 1996. Ontogeny of feeding and respiration in larval Atlantic cod (Gadus morhua) (Teleostei, Gadiformes): I. Morphology. J. Morphology 227: 15-35.

    Google Scholar 

  • Hunter, J.R. 1981. Feeding ecology and predation of marine fish larvae. pp. 33-77. In: R. Lasker (ed.) Marine Fish Larvae: Morphology, Ecology and Relation to Fisheries, Washington Sea Grant Program, Seattle.

    Google Scholar 

  • Kendall, A.W., E.H. Ahlstrom & H.G. Moser. 1984. Early life history stages of fishes and their characters. pp. 11-22. In: H.G. Moser (ed.) Ontogeny and Systematics of Fishes, American Society of Ichthyologists and Herpetologists Special Publication No. 1, Allen Press, Lawrence.

    Google Scholar 

  • Kiorboe, T.K., P. Munk, & J.G. Stottrup. 1985. First feeding by larval herring (Clupea harengus L.). Dana 5: 95-107.

    Google Scholar 

  • Lasker, R. 1975. Field criteria for survival of anchovy larvae: The relation between inshore chlorophyll maximum layers and successful first feeding. U.S. Fish. Bull. 73: 453-462.

    Google Scholar 

  • Lough, R.G. & D.G. Mountain. 1996. Effect of small-scale turbulence on feeding rates of larval cod and haddock in stratified water on Georges Bank. Deep-Sea Research. 43: 1745-1772.

    Google Scholar 

  • Mayer, C.M. & D.H. Wahl. 1997. The relationship between prey selectivity and growth and survival in a larval fish. Can. J. Fish. Aquat. Sci. 54: 1504-1512.

    Google Scholar 

  • McDowell, E.M. & B.F. Trump. 1976. Histologic fixatives suitable for diagnostic light and electron microscopy. Arch. Path. Lab. Med. 100: 405-414.

    Google Scholar 

  • Murdoch, W.W. 1971. The developmental response of predators to changes in prey density. Ecology 52: 132-135.

    Google Scholar 

  • Overstreet, R.M. & R.W. Heard. 1978. Food of the red drum (Sciaenops ocellata) from Mississippi sound. Gulf Res. Rep. 6: 131-135.

    Google Scholar 

  • Pearson, J.C. 1928. Natural history and conservation of the redfish and other commercial sciaenids on the Texas coast. Bull. U.S. Bur. Fish. 44: 129-214.

    Google Scholar 

  • Pepin, P. & R.W. Penney. 1997. Patterns of prey size and taxonomic composition in larval fish: Are there general size dependent models? J. Fish Biol. (Supp. A) 51: 84-100.

    Google Scholar 

  • Peters, K.M. & R.H. McMichael, Jr. 1987. Early life history of the red drum (Sciaenops ocellatus) (Pisces: Sciaenidae), in Tampa Bay, Florida. Estuaries 10: 92-107.

    Google Scholar 

  • Pryor, V.K. & C.E. Epifanio. 1993. Prey selection by larval weak-fish (Cynoscion regalis): The effects of prey size, speed and abundance. Mar. Biol. 116: 31-37.

    Google Scholar 

  • Rice, J.A., L.B. Crowder & M.E. Holey. 1987. Exploration of mechanisms regulating larval survival in Lake Michigan bloater:Arecruitment analysis based on characteristics of individual larvae. Trans. Amer. Fish. Soc. 116: 703-718.

    Google Scholar 

  • Schael, D.M., L.G. Rudstam & J.R. Post. 1991. Gape limitation and prey selection in larval yellow perch (Perca flavescens), freshwater drum (Aplodinotus grunniens) and black crappie (Pomoxis nigromaculatus). Can. J. Fish. Aquat. Sci. 48: 1919-1925.

    Google Scholar 

  • Shirota, A. 1970. Studies on the mouth size of fish in the larval and fry stages. Bull. Jap. Soc. Sci. Fish. 36: 353-368 (translation of the Fisheries Research Board of Canada No. 1978).

    Google Scholar 

  • Soto, M.A., G.J. Holt, S.A. Holt & J. Rooker. 1998. Food habits and dietary overlap of newly settled red drum (Sciaenops ocellatus) and Atlantic croaker (Micropogonius undulatus) from Texas seagrass meadows. Gulf Res. Rep. 10: 41-55.

    Google Scholar 

  • Steen, J.P. & J.L. Laroche. 1983. The food of red drum (Sciaenops ocellatus) larvae and early juveniles taken from the Mississippi Sound and the northern Gulf of Mexico. pp. 35-38. In: S.V. Shabica, N.B. Cofer & E.W. Cake, Jr. (ed.) Proceedings of the Northern Gulf of Mexico Estuaries and Barrier Islands Research Conference, United States Department of the Interior, Atlanta.

    Google Scholar 

  • Welker, M.T., C.L. Pierce & D.H. Wahl. 1994. Growth and survival of larval fishes: Roles of competition and zooplankton abundance. Trans. Amer. Fish. Soc. 123: 703-717.

    Google Scholar 

  • Wong, B. & F.J. Ward. 1972. Size selection of Daphnia pulicaria by yellow perch (Perca flavescens) fry in west Blue Lake, Manitoba. J. Fish. Res. Board Can. 30: 1761-1764.

    Google Scholar 

  • Yokel, B.J. 1966. A contribution to the biology and distribution of the red drum (Sciaenops ocellata). M.S. Thesis, University of Miami, Miami. 166 pp.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Krebs, J.M., Turingan, R.G. Intraspecific variation in Gape–prey size Relationships and Feeding Success During Early Ontogeny in Red Drum, Sciaenops Ocellatus . Environmental Biology of Fishes 66, 75–84 (2003). https://doi.org/10.1023/A:1023290226801

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1023290226801

Navigation