Skip to main content
Log in

Body size and microclimate use in Neotropical granivorous ants

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

Abstract

The stability of tropical microclimates has left microclimate use by tropical species little unexplored. At La Selva Costa Rica, I related foraging activity at seed baits to humidity in two forests types. I recorded 38 and 35 ant species at seed baits in closed and open canopy forest. The microclimate 5 cm above the forest floor in the younger, Open Forest was warmer, drier, more variable, and more sensitive to current weather than in the older Closed Forest. Ant species within both forests foraged at different Vapor Pressure Deficits (kPa), a measure of the drying power of the air. VPD use was not confounded with diel activity patterns. Body size explained 46% of the variance in mean VPD use among ant species. Small ant species tended to forage in moist microclimates; large species tended to be microclimate generalists. Larger species were also more active in the drier Open Forest. Foraging activity by these assemblages varies 4-fold, and peaks close to the mean VPD for each habitat. The behavior of these assemblages suggest that 1) small ant species at La Selva potentially compete with the entire range of ant body sizes, whereas large ants forage when and where small ants are inactive; and 2) seeds dispersed to the forest floor at dawn will be consumed or further dispersed by a larger suite of ants species than those falling in the heat of the tropical afternoon.

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

  • Andersen AN (1992) Regulation of “momentary” diversity by dominant species in exceptionally rich ant communities of the Australian seasonal tropics. Am Nat 140:401–420

    Google Scholar 

  • Andrewartha HG, Birch LC (1954) The Distribution and Abundance of Animals. University of Chicago Press, Chicago

    Google Scholar 

  • Beattie AJ (1985) The evolutionary ecology of ant-plant mutualisms. Cambridge University Press, Cambridge

    Google Scholar 

  • Briese DT, Macauley BJ (1980) Temporal structure of an ant community in semi arid Australia. Austral J Ecol 5:121–134

    Google Scholar 

  • Brown JH, Maurer BA (1986) Body size, ecological dominance and Cope's rule. Nature 324:699–700

    Google Scholar 

  • Byrne MM (1991) Ecology and coexistence mechanisms of tropical twig-dwelling ants. M.S. University of Florida, Gainesville, USA

  • Calder WA III (1984) Size, function, and life history. Harvard University Press, Cambridge, USA

    Google Scholar 

  • Cambell GS (1977) An introduction to environmental biophysics. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Cherrett JM (1986) History of the leaf cutting ant problem. In: C.S. Lofgren and R.K. Vander Meer (ed) Fire ants and leaf cutting ants: biology and management. Westview Press, Boulder

    Google Scholar 

  • Crawford CS, Wooten RC (1973) Water relations in Diplocentrus spitzeri, a semimontane scorpion from the Southwestern United States. Phys Zool 6:218–229

    Google Scholar 

  • Davidson DW (1977) Species diversity and community organization in desert seed-eating ants. Ecology 58:711–724

    Google Scholar 

  • Edney EB (1971) Some aspects of water balance in tenebrionid beetles and a thysanuran from the Namib Desert of South Africa. Phys Zool 44:61–76

    Google Scholar 

  • Edney EB (1977) Water balance in land arthropods. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Fetcher N, Oberbauer SF, Strain BR (1985) Vegetation effects on microclimate in lowland tropical forest in Costa Rica. Int J Biometeorol 29:145–155

    Google Scholar 

  • Franks NR, Bossert WH (1983) The influence of swarm raiding army ants on the patchiness and diversity of a tropical leaf litter ant community Sutton EL, Whitmore TC, Chadwick AC (eds) pp 151–163

  • Geiger R (1965) The climate near the ground. Harvard University Press, Cambridge

    Google Scholar 

  • Gentry AH (1988) Changes in plant community diversity and floristic composition on environmental and geographic gradients. Ann Mo Bot Gard 75:1–34

    Google Scholar 

  • Hartshorn GS (1983) Introduction to Plants. In: Janzen DH (ed) Costa Rican Natural History. University of Chicago Press, Chicago, USA

    Google Scholar 

  • Herreid CF (1969) Integumental permeability of crabs and adaptation to land. Comp Biochem Physiol 29:423–429

    Google Scholar 

  • Holdridge LR, Grenke WC, Hatheway WH, Liang T, Tosi JAJ (1971) Forest environments in tropical life zones: a pilot study. Pergamon Press, New York, USA

    Google Scholar 

  • Hölldobler B, Wilson EO (1990) The Ants. Belknap Press, Cambridge

    Google Scholar 

  • Hood WG, Tschinkel WR (1990) Desiccation resistance in arboreal and terrestrial ants. Physiological Entomology 15:23–35

    Google Scholar 

  • Hutchinson GE, MacArthur RH (1959) A theoretical ecological model of size distributions among species of animals. Am Nat 93:117–125

    Google Scholar 

  • Janzen DH, (1967) Why mountain passes are so high in the tropics. Am Nat 101:233–249

    Google Scholar 

  • Junzen DH (1973) Sweep samples of tropical foliage insects: effects of seasons, vegetation types, elevation, time of day, and insularity. Ecology 54:687–708

    Google Scholar 

  • Janzen DH, Schoener TW (1968) Differences in insect abudance and diversity between wetter and drier sites during a tropical dry season. Ecology 49:96–110

    Google Scholar 

  • Jeanne RL (1979) A latitudinal gradient in rates of ant predation. Ecology 60:1211–1224

    Google Scholar 

  • Karr JR, Freemark KE (1983) Habitat selection and environmental gradients. Ecology 64:1481–1494

    Google Scholar 

  • Kaspari M (1992) Niche relationships in an assemblage of neotropical granivorous ants. Ph. D. Dissertation, University of Arizona, Tucson, USA

  • Kaspari M (1993) Removal of seeds from Neotropical frugivore droppings: ant responses to seed number. Oecologia 95:81–88

    Google Scholar 

  • Levey DJ, Byrne MM (1993) Complex ant-plant interactions: Pheidole as secondary dispersers and postdispersal seed predators of rain forest plants. Ecology 74:1802–1812

    Google Scholar 

  • Levings SC, Windsor DM (1984) Litter moisture content as a determinant of litter arthropod distribution and abundance during the dry season on Barro Colorado Island, Panama. Biotropica 16:125–131

    Google Scholar 

  • Longino JT, Nadkarni NM (1990) A comparison of ground and canopy leaf litter ants (Hymenoptera: Formicidae) in a neotropical montane forest. Psyche 97:81–92

    Google Scholar 

  • MacArthur RH (1972) Geographical Ecology. Princeton University Press, Princeton

    Google Scholar 

  • May RM (1978) The dynamics and diversity of insect faunas. Pages 188–204. in L.A. Mound, N. Waloff. Diversity of Insect Faunas. Blackwell Scientific, New York

    Google Scholar 

  • Morton SR, Davidson DW (1988) Comparative structure of harvester ant communities in arid Australia and North America. Ecol Mono 58:19–38

    Google Scholar 

  • Pianka ER (1966) Latitude gradients in tropical diversity: a review of concepts. Am Nat 100:33–46

    Google Scholar 

  • Porter SD, Tschinkel WR (1987) Foraging in Solenopsis invicta (Hymenoptera: Formicidae): effects of weather and season. Enviromental Entomology 16:802–808

    Google Scholar 

  • Rissing SW, Pollock GB (1984) Worker size variability and foraging efficiency in Veromessor pergandei (Hymenoptera: Formicidae). Behav Ecol Sociobiol 15:121–126

    Google Scholar 

  • Rosenberg NJ (1974) Microclimate: the biological environment. Wiley Interscience, New York

    Google Scholar 

  • Schoener TW, Janzen DH (1968) Notes on environmental determinants of tropical versus temperate insect size patterns. Am Nat 102:206–224

    Google Scholar 

  • Schumacher A, Whitford WG (1976) Spatial and temporal variation in Chihuahuan ant faunas. Southw Nat 21:1–8

    Google Scholar 

  • Stevens GC (1989) The latitudinal gradient in geographical range: how so many species coexist in the tropics. Am Nat 133:246–256

    Google Scholar 

  • Talbot M (1934) Distribution of ant species in the Chicago region with reference to ecological factors and physiological toleration. Ecology 15:416–439

    Google Scholar 

  • Tennant LE, Porter SD (1991) Comparison of diets of two fire ant species (Hymenoptera: Formicidae): solid and liquid components. J Entomol Sci 26:450–465

    Google Scholar 

  • Whitford WG, Ettershank G (1975) Factors affecting foraging activity in Chihuahuan desert harvester ants. Env Entomol 4:689–696

    Google Scholar 

  • Whittaker RH (1970) Communities and Ecosystems. Macmillan, New York

    Google Scholar 

  • Wigglesworth VB (1945) Transpiration through the cuticle of insects. J Exp Biol 21:97–114

    Google Scholar 

  • Wilson DS (1975) The adequacy of body size as a niche difference. Am Nat 109:769–784

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kaspari, M. Body size and microclimate use in Neotropical granivorous ants. Oecologia 96, 500–507 (1993). https://doi.org/10.1007/BF00320507

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00320507

Key words

Navigation