Skip to main content
Log in

Population processes in a large herbivorous reptile: the giant tortoise of Aldabra atoll

  • Original Papers
  • Published:
Oecologia Aims and scope Submit manuscript

Summary

Physical barriers divide the population of giant tortoises (Geochelone gigantea Schweigger) on Aldabra into several sub-populations of different density, which nevertheless are similar genetically. We measured individual growth rates in each sub-population. Mortality was estimated using data from Bourn and Coe (1979). Reproduction and recruitment were studied using data from previous work (Swingland and Coe 1979) and our own estimates of clutch size, egg weight, and laying frequency from 1975 to 1981.

Individual growth rates were strongly dependent only on individual size and sub-population density and not on age or sex. Within a sub-population, the relationship between specific growth rate and size (linear measure) was best fitted by a Gompertz model, except for very young tortoises which grew faster in volume, though not in weight, than expected. Animals at high densities grow slowly to a small size whereas those at low densities grow fast to a large size. At very high density many juveniles remain at a small size without growing or maturing.

Mortality of larger (> ca. 5 years old) animals was independent of density, but did depend on size in the highest-density sub-population, as predicted by the Gompertz growth model.

Reproduction and recruitment were negatively density-dependent over the whole density range (5 to 35 animals ha-1) studied. Clutch size and laying frequency were strongly influenced by sub-population density, but egg weight was not. Laying frequency varied within sub-populations according to rainfall (presumably via annual food supply).

All except one sub-population are seen as stages in the development of the same interactive system. Competition between individuals is nearly, but not purely, of scramble type. The remaining sub-population is either a distinct interactive system in which food supply for very young animals is important, or it is a non-interactive system controlled by the effect of natural enemies on very young animals. This suggests that the equilibrium density and/or dynamics of giant tortoise populations are highly sensitive to mortality factors affecting very young animals.

In low density sub-populations the animals are large, have many young, low relative reproductive effort, and a short generation time. In high density sub-populations they are small, have few young, high relative reproductive effort, and a long generation time. This variation is largely phenotypic. It is anomalous with respect to r-K life history theory but is a logical consequence of indeterminate growth combined with size-determined risk and benefit functions and may have contributed to the giant tortoises' success as island colonisers.

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

References

  • Abbott WL (1893) Notes on the natural history of Aldabra, Assumption and Glorioso islands, Indian Ocean. Proc US natn Mus 15:759–764

    Google Scholar 

  • Arnold EN (1979) Indian Ocean giant tortoises: their systematics and island adaptations. Phil Trans R Soc Lond B 286:127–145

    Google Scholar 

  • Bourn DM (1976) The giant tortoise population of Aldabra (Cryptodira: Testudinidae). Part 1: preliminary results. Zoologica Africana 11:275–284

    Google Scholar 

  • Bourn DM, Coe MJ (1978) The size, structure and distribution of the giant tortoise population of Aldabra. Phil Trans R Soc Lond B 282:139–175

    Google Scholar 

  • Bourn DM, Coe MJ (1979) Features of tortoise mortality and decomposition on Aldabra. Phil Trans R Soc Lond B 286:189–193

    Google Scholar 

  • Carlquist S (1974) Island Biology. Columbia University Press, New York

    Google Scholar 

  • Caughley G, Lawton JH (1981) Plant-Herbivore Systems. In: May RM (ed) Theoretical Ecology (2nd edition). Blackwell Scientific, Oxford

    Google Scholar 

  • Coe MJ, Bourn DM, Swingland IR (1979) The biomass, production and carrying capacity of giant tortoises on Aldabra. Phil Trans R Soc Lond B 286:163–176

    Google Scholar 

  • Frazier JG (1971) Behavioural and ecological observations on Giant tortoises on Aldabra atoll. Unpublished DPhil thesis, University of Oxford

  • Gaymer R (1973) A marking method for giant tortoises and field trials on Aldabra. J Zool Lond 169:393–401

    Google Scholar 

  • Gibson CWD, Guilford TC, Hambler C, Sterling PH (1983) Transition matrix models and succession after release from grazing on Aldabra atoll. Vegetatio 52:151–159

    Google Scholar 

  • Gibson CWD, Hamilton J (1983) Feeding ecology and seasonal movements of giant tortoises on Aldabra atoll. Oecologia (Berlin) 56:84–92

    Google Scholar 

  • Gibson CWD, Phillipson J (1983a) The vegetation of Aldabra atoll: preliminary analysis and construction of the vegetation map. Phil Trans R Soc Lond B 302:201–235

    Google Scholar 

  • Gibson CWD, Phillipson J (1983b) The primary production of Aldabra atoll, with special reference to habitats used by giant tortoises. Phil Trans R Soc Lond B 302:167–199

    Google Scholar 

  • Grubb P (1971) The growth, ecology and population structure of giant tortoises on Aldabra. Phil Trans R Soc Lond B 260:327–372

    Google Scholar 

  • Halliday T (1978) Vanishing Birds. Sidgwick and Jackson

  • Hamilton J, Coe MJ (1982) Feeding, digestion and assimilation of a population of giant tortoises (Geochelone gigantea Schweigger) on Aldabra atoll. J Arid Environments 5:127–144

    Google Scholar 

  • Hendrickson JR (1958) The green sea turtle Chelonia mydas (Linn.) in Malaya and Sarawak. Proc Zool Soc Lond 130 pt 4:455–535

    Google Scholar 

  • Hnatiuk RJ (1979) Temporal and spatial variation in precipitation on Aldabra Phil Trans R Soc Lond B286:25–34

    Google Scholar 

  • Hnatiuk RJ, Woodell SRJ, Bourn DM (1976) Giant tortoise and vegetation interactions on Aldabra atoll-Part 2:Coastal Biol Conserv 9:305–316

    Google Scholar 

  • Hughes GM, Gaymer R, Moore M, Weakes AJ (1971) Respiratory exchange and body size in the Aldabran giant tortoise. J Exp Biol 55:651–665

    Google Scholar 

  • Kaufmann KW (1981) Fitting and using growth curves. Oecologia (Berlin) 49:293–299

    Google Scholar 

  • Lawton JH, McNeill S (1979) Between the devil and the deep blue sea: on the problems of being a herbivore. In Anderson RM, Turner BD, Taylor LR (eds) Population Dynamics. Symp Brit Ecol Soc 20: Blackwell Scientific, Oxford, pp 223–244

    Google Scholar 

  • MacArthur RH, Wilson EO (1967) The Theory of Island Biogeography. Princeton University Press

  • Monro J (1967) The exploitation and conservation of resources by populations of insects. J Anim Ecol 36:531–547

    Google Scholar 

  • Snow DW (1964) Research Station in the Galapagos: the Giant Tortoises of the Galapagos Islands, their present status and future conservation. Oryx VII, 6:275–290

    Google Scholar 

  • Southwood TRE (1981) Bionomic strategies. In: May RM (ed) Theoretical Ecology (2nd edition). Blackwell Scientific, Oxford

    Google Scholar 

  • Stearns SC (1983a) The evolution of life history traits in mosquitofish since their introduction to Hawaii in 1905; Rates of evolution, heritabilities and developmental plasticity. In Stearns SC (1983b) pp 65–75

  • Stearns SC (1983b) The interface of life-history evolution, whole organism ontogeny and quantitative genetics. Symp Amer Soc of Zoologists. Amer Zool 23, 1, pp 1–125

    Google Scholar 

  • Stoddart DR, Cowx D, Peet C, Wilson JD (1982) Tortoises and Tourists in the western Indian Ocean: the Curieuse Experiment. Biol Conserv 24, 1, 67–79

    Google Scholar 

  • Stoddart DR, Mole LU (1977) Climate of Aldabra atoll. Atoll Res Bull 202:1–21

    Google Scholar 

  • Stoddart DR, Peake JF (1979) Historical records of Indian Ocean giant tortoise populations. Phil Trans R Soc Lond B286:147–162

    Google Scholar 

  • Stoddart DR, Walsh RPD (1979) Long-term climatic change in the western Indian Ocean. Phil Trans R Soc Lond B286:11–24

    Google Scholar 

  • Swingland IR (1977) Reproductive effort and life history strategy of the Aldabran giant tortoise. Nature London 269:402–404

    Google Scholar 

  • Swingland IR, Coe MJ (1978) The natural regulation of giant tortoise populations on Aldabra atoll; recruitment. Phil Trans R Soc Lond B286:177–188

    Google Scholar 

  • Swingland IR, Lessels CM (1979) The natural regulation of giant tortoise populations on Aldabra atoll; Movement polymorphism, reproductive success and mortality. J Anim Ecol 48:639–654

    Google Scholar 

  • Voeltzkow A (1897) Einleitung. Madagaskar. Juan de Nova. Aldabra Abh Senckenb naturf Ges 21:1–76

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Gibson, C.W.D., Hamilton, J. Population processes in a large herbivorous reptile: the giant tortoise of Aldabra atoll. Oecologia 61, 230–240 (1984). https://doi.org/10.1007/BF00396766

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00396766

Keywords

Navigation