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Energetic constraints on the diet of terrestrial carnivores

Author

Listed:
  • Chris Carbone

    (Institute of Zoology, Zoological Society of London
    Wildlife Conservation Research Unit, University of Oxford)

  • Georgina M. Mace

    (Institute of Zoology, Zoological Society of London)

  • S. Craig Roberts

    (Institute of Zoology, Zoological Society of London)

  • David W. Macdonald

    (Wildlife Conservation Research Unit, University of Oxford)

Abstract

Species in the mammalian order Carnivora exhibit a huge diversity of life histories with body sizes spanning more than three orders of magnitude. Despite this diversity, most terrestrial carnivores can be classified as either feeding on invertebrates and small vertebrates or on large vertebrates. Small carnivores feed predominantly on invertebrates probably because they are a superabundant resource (sometimes 90% of animal biomass1,2,3); however, intake rates of invertebrate feeders are low, about one tenth of those of vertebrate feeders4,5. Although small carnivores can subsist on this diet because of low absolute energy requirements, invertebrate feeding appears to be unsustainable for larger carnivores. Here we show, by reviewing the most common live prey in carnivore diets, that there is a striking transition from feeding on small prey (less than half of predator mass) to large prey (near predator mass), occurring at predator masses of 21.5–25 kg. We test the hypothesis that this dichotomy is the consequence of mass-related energetic requirements and we determine the predicted maximum mass that an invertebrate diet can sustain. Using a simple energetic model and known invertebrate intake rates, we predict a maximum sustainable mass of 21.5 kg, which matches the point where predators shift from small to large prey.

Suggested Citation

  • Chris Carbone & Georgina M. Mace & S. Craig Roberts & David W. Macdonald, 1999. "Energetic constraints on the diet of terrestrial carnivores," Nature, Nature, vol. 402(6759), pages 286-288, November.
  • Handle: RePEc:nat:nature:v:402:y:1999:i:6759:d:10.1038_46266
    DOI: 10.1038/46266
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    Cited by:

    1. Alexandra McQueen & Marcel Klaassen & Glenn J. Tattersall & Robyn Atkinson & Roz Jessop & Chris J. Hassell & Maureen Christie & Matthew R. E. Symonds, 2022. "Thermal adaptation best explains Bergmann’s and Allen’s Rules across ecologically diverse shorebirds," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Matthew R Borths & Erik R Seiffert, 2017. "Craniodental and humeral morphology of a new species of Masrasector (Teratodontinae, Hyaenodonta, Placentalia) from the late Eocene of Egypt and locomotor diversity in hyaenodonts," PLOS ONE, Public Library of Science, vol. 12(4), pages 1-60, April.
    3. Gregor Kalinkat & Björn Christian Rall & Olivera Vucic-Pestic & Ulrich Brose, 2011. "The Allometry of Prey Preferences," PLOS ONE, Public Library of Science, vol. 6(10), pages 1-11, October.
    4. Karami, Peyman & Tavakoli, Sajad, 2022. "Identification and analysis of areas prone to conflict with wild boar (Sus scrofa) in the vineyards of Malayer County, western Iran," Ecological Modelling, Elsevier, vol. 471(C).

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