Skip to main content
Log in

Limited flexibility and unusual longevity shape forager allocation in the Florida harvester ant (Pogonomyrmex badius)

  • Original Article
  • Published:
Behavioral Ecology and Sociobiology Aims and scope Submit manuscript

Abstract

The benefits of behavioral flexibility in social insect societies are well known, but the advantages of limited flexibility have seldom been considered. Florida harvester ant colonies maintain a stable forager population size for much of their active season, and despite seasonal variation in chronological age, foragers die within 27 days of initiating foraging. To determine how colonies balance forager mortality and forager replacement, we tested the relative influences of intrinsic and extrinsic factors on forager membership, retention, and longevity. Potential and realized forager longevity differed significantly. Residual lifespan increased by 57 % when colonies were penned for 20 days, and up to 8-fold when foragers were retained in the laboratory. Increased forager longevity inhibited the movement of new workers into the forager population. In contrast, increased mortality and starvation did not stimulate the addition of new foragers and forager population size declined when mortality exceeded 4 % per day. Experimental increases in forager number, body fat, and the ratio of larvae to foragers did not induce behavioral reversion in existing foragers. These results suggest an unidirectional allocation strategy, with foragers that are less disposable and less behaviorally flexible than the well-studied honey bee. In P. badius, forager membership is maintained not by young ants detecting increased demand, but by workers developing at rates that allow forager replacement and prevent excessive worker depletion. In the absence of a lifespan matched to predictable risks, opportunistic increases in forager survival may promote colony growth by inhibiting the scheduled and irreversible transitions of younger workers.

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

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11

Similar content being viewed by others

References

  • Amdam GV, Rueppell O, Fondrk MK, Page RE, Nelson CM (2009) The nurse’s load: early life exposure to brood-rearing affects behavior and lifespan in honey bees (Apis mellifera). Exp Gerontol 44:467–471

    Article  PubMed  PubMed Central  Google Scholar 

  • Bernadou A, Busch J, Heinze J (2015) Diversity in identity: behavioral flexibility, dominance, and age polyethism in a clonal ant. Behav. Ecol. Sociobiol: 1-11

  • Blanchard GB, Orledge GM, Reynolds SE, Franks NR (2000) Division of labour and seasonality in the ant Leptothorax albipennis: worker corpulence and its influence on behaviour. Animal Behav 59:723–738

    Article  Google Scholar 

  • Calderone NW (1995) Temporal division of labor in the honey bee, Apis mellifera: a developmental process or the result of environmental influences? Can J Zool 73:1410–1416

    Article  Google Scholar 

  • Couvillon MJ, Jandt JM, Bonds J, Helm BR, Dornhaus A (2011) Percent lipid is associated with body size but not task in the bumble bee Bombus impatiens. J Comp Physiol A 197(11):1097–1104

    Article  CAS  Google Scholar 

  • Dolezal AG, Brent CS, Hölldobler B, Amdam GV (2012) Worker division of labor and endocrine physiology are associated in the harvester ant, Pogonomyrmex californicus. The J of Exp Bio 215(3):454–460

    Article  CAS  Google Scholar 

  • Dukas R (2008) Mortality rates of honey bees in the wild. Insectes Soc 55:252–255

    Article  Google Scholar 

  • Free JB, Spencer-Booth Y (1959) The longevity of worker honey bees (Apis mellifera). Proc R Entomol Soc London 34(A):141–150

  • Gentry JB (1974) Response to predation by colonies of the Florida harvester ant, Pogonomyrmex badius. Ecology 55:1328–1338

    Article  Google Scholar 

  • Giraldo YM, Traniello JF (2014) Behav Ecol Sociobiol 68(12):1901–1919

    Article  PubMed  PubMed Central  Google Scholar 

  • Gordon DM, Hölldobler B (1987) Worker longevity in harvester ants (Pogonomyrmex). Psyche 94:341–346

    Article  Google Scholar 

  • Gordon DM, Chu J, Lillie A, Tissot M, Pinter N (2005) Variation in the transition from inside to outside work in the red harvester ant Pogonomyrmex barbatus. Insect Soc 52:212–217

    Article  Google Scholar 

  • Harrison JS, Gentry JB (1981) Foraging pattern, colony distribution, and foraging range of the Florida harvester ant, Pogonomyrmex badius. Ecology 62:1467–1473

    Article  Google Scholar 

  • Hölldobler B, Wilson EO (1971) Recruitment trails in the harvester ant Pogonomyrmex badius. Psyche 77:385–399

    Article  Google Scholar 

  • Hölldobler B, Wilson EO (1990) The Ants. The Belknap Press of Harvard University Press, Cambridge, MA

    Book  Google Scholar 

  • Howard DF, Tschinkel WR (1981) The flow of food in colonies of the fire ant, Solenopsis invicta: a multifactorial study. Physiol Entomol 6:297–306

    Article  Google Scholar 

  • Huang Z, Robinson GE (1996) Regulation of honey bee division of labor by colony age demography. Behav Ecol Sociobiol 39:147–158

    Article  Google Scholar 

  • Kirkwood TBL (1977) Evolution of ageing. Nature 270:301–310

    Article  PubMed  CAS  Google Scholar 

  • Kirkwood TBL, Austad SN (2000) Why do we age? Nature 408:233–238

    Article  PubMed  CAS  Google Scholar 

  • Kwapich CL, Tschinkel WR (2013) Demography, demand, death, and the seasonal allocation of labor in the Florida harvester ant (Pogonomyrmex badius). Behav Ecol and Sociobiol 67:2011–2027

    Article  Google Scholar 

  • Lee RD (2003) Rethinking the evolutionary theory of aging: transfers, not births, shape senescence in social species. Proc Natl Acad Sci U S A 100:9637–9642

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Leoncini I, Le Conte Y, Costagliola G, Plettner E, Toth AL, Wang M, Huang Z, Bécard J-M, Crauser D, Slessor KN, Robinson GE (2004) Regulation of behavioral maturation by a primer pheromone produced by adult worker honey bees. Proc Natl Acad Sci U S A 101:17559–17564

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Lincoln FC (1930) Calculating Waterfowl Abundance on the Basis of Banding Returns. United States Department of Agriculture Circular 118, Washington D.C., pp 1–4

    Google Scholar 

  • Maurizio A (1950) The influence of pollen feeding and brood rearing on the length of life and physiological conditions of the honeybee. Bee World 31:9–12

    Article  Google Scholar 

  • Medawar PB (1952) An unsolved problem in biology. Lewis, London

    Google Scholar 

  • Mersch DP, Crespi A, Keller L (2013) Tracking individuals shows spatial fidelity is a key regulator of ant social organization. Science 340:1090–1093

    Article  PubMed  CAS  Google Scholar 

  • Münch D, Amdam GV (2010) The curious case of aging plasticity in honey bees. FEBS Lett 584:2496–2503

    Article  PubMed  Google Scholar 

  • Münch D, Kreibich CD, Amdam GV (2013) Aging and its modulation in a long-lived worker caste of the honey bee. J Exp Biol 216(9):1638–1649

    Article  PubMed  PubMed Central  Google Scholar 

  • Oettler J, Johnson RA (2009) The old ladies of the seed harvester ant Pogonomyrmex rugosus: foraging performed by two groups of workers. J Insect Behav 22:217–226

    Article  PubMed  PubMed Central  Google Scholar 

  • Oster GF, Wilson EO (1978) Caste and ecology in the social insects. Princeton University Press, Princeton

    Google Scholar 

  • Porter SD, Jorgensen CD (1981) Foragers of the harvester ant, Pogonomyrmex owyheei: a disposable caste? Behav Ecol Sociobiol 9:247–256

    Article  Google Scholar 

  • R Core Team (2013). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. URL http://www.R-project.org/.

  • Remolina SC, Hafez DM, Robinson GE, Hughes KA (2007) Senescence in the worker honey bee Apis mellifera. J Insect Physiol 53:1027–1033

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  • Robinson GE, Page RE, Strambi C, Strambi A (1992) Colony integration in honey bees: mechanisms of behavioral reversion. Ethology 90:336–348

    Article  CAS  Google Scholar 

  • Robinson GE, Huang ZY (1998) Colony integration in honey bees: genetic, endocrine and social control of division of labor. Apidologie, Springer Verlag 29(1-2):159–170

    Article  Google Scholar 

  • Rüppell O, Kirkman R (2005) Extraordinary starvation resistance in Temnothorax rugatulus (Hymenoptera, Formicidae) colonies: demography and adaptive behavior. Insectes Soc 52:282–290

    Article  Google Scholar 

  • Rüppell O, Bachelier C, Fondrk MK, Page RE Jr (2007) Regulation of life history determines lifespan of worker honey bees (Apis mellifera L.). Exp Gerontol 42:1020–1032

    Article  Google Scholar 

  • Schmid-Hempel P (1983). Foraging ecology and colony structure of two sympatric species of desert ants, Cataglyphis bicolor and Cataglyphis albicans, Doctoral Dissertation, Universität Zürich

  • Schmid-Hempel P, Schmid-Hempel R (1984) Life duration and turnover of foragers in the ant Cataglyphis bicolor (Hymenoptera, Formicidae). Insectes Soc 31:345–360

    Article  Google Scholar 

  • Seeley TD (1982) Adaptive significance of the age polyethism schedule in honeybee colonies. Behav Ecol Sociobiol 11:287–293

    Article  Google Scholar 

  • Seid MA, Traniello JFA (2006) Age-related repertoire expansion and division of labor in Pheidole dentata (Hymenoptera: Formicidae): a new perspective on temporal polyethism and behavioral plasticity in ants. Behav Ecol Sociobiol 60:631–644

    Article  Google Scholar 

  • Smith CR, Tschinkel WR (2006) The sociometry and sociogenesis of reproduction in the Florida harvester ant, Pogonomyrmex badius. J Insect Sci 6(32):11

    Article  Google Scholar 

  • Smith CR (2007) Energy use and allocation in the Florida harvester ant, Pogonomyrmex badius: are stored seeds a buffer? Behav Ecol Sociobiol 61:1479–1487

    Article  Google Scholar 

  • Smith CR, Schoenick C, Anderson KE, Gadau J, Suarez AV (2007) Potential and realized reproduction by different worker castes in queen-less and queen-right colonies of Pogonomyrmex badius. Insectes Soc 54:260–267

    Article  Google Scholar 

  • Smith CR, Suarez AV (2010) The trophic ecology of castes in harvester ant colonies. Funct Ecol 24:122–130

    Article  Google Scholar 

  • Smith CR, Tschinkel WR (2009) Ant fat extraction with a Soxhlet extractor. Cold Spring Harb Protoc 2009(7):5243–5247

    Google Scholar 

  • Traniello JFA, Rosengaus RB (1997) Ecology, evolution, and division of labour in social insects. Anim Behav 53:209–213

    Article  Google Scholar 

  • Tschinkel WR (1988a) Seasonal life history and nest architecture of a winter-active ant, Prenolepis imparis. Insectes Soc 34:143–164

    Article  Google Scholar 

  • Tschinkel WR (1988b) Social control of egg-laying rate in queens of the fire ant, Solenopsis invicta. Physiol Entomol 13:327–350

    Article  Google Scholar 

  • Tschinkel WR, Porter SD (1988) Efficiency of sperm use in queens of the fire ant, Solenopsis invicta (Hymenoptera: Formicidae). Ann Entomol Soc Am 81:777–781

    Article  Google Scholar 

  • Tschinkel WR (1995) Stimulation of fire ant queen fecundity by a highly specific brood stage. Ann Entomol Soc Am 88(6):876–882

    Article  Google Scholar 

  • Tschinkel WR (1998) Sociometry and sociogenesis of colonies of the harvester ant, Pogonomyrmex badius: worker characteristics in relation to colony size and season. Insectes Soc 45:385–410

    Article  Google Scholar 

  • Tschinkel WR (1999) Sociometry and sociogenesis of colonies of the harvester ant, Pogonomyrmex badius: distribution of workers, brood and seeds within the nest in relation to colony size and season. Ecol Entomol 24:222–237

    Article  Google Scholar 

  • Tschinkel WR (2006) The fire ants. Harvard University Press, Cambridge, MA, pp 747–716

    Google Scholar 

  • Tschinkel WR (2010) The organization of foraging in the fire ant, Solenopsis invicta. J Insect Sci 10:26

    Google Scholar 

  • Tschinkel WR (2011) Back to basics: sociometry and sociogenesis of ant societies (Hymenoptera: Formicidae). Myrmecol News 14:49–54

    Google Scholar 

  • Tschinkel WR (2015) Biomantling and bioturbation by colonies of the Florida harvester ant, Pogonomyrmex badius. PlosOne 10(3):e0120407. doi:10.1371/journal.pone.0120407

    Article  Google Scholar 

  • Tschinkel WR, Rink WJ, Kwapich CL (2015) Sequential subterranean transport of excavated sand and foraged seeds in nests of the harvester ant, Pogonomyrmex badius. PLoS ONE 10(10):e0139922. doi:10.1371/journal.pone.0139922

  • Wehner R, Harkness RD, Schmid-Hempel P (1983) Foraging strategies in individually searching ants, Cataglyphis bicolor (Hymenoptera, Formicidae). In: Lindauer M (ed) Information Processing in Animals. Fischer, Stuttgart, pp 1–79

    Google Scholar 

  • Whitford WG, Bryant M (1979) Behavior of a predator and its prey: The horned Lizard (Phrynosoma Cornutum) and harvester ants (Pogonomyrmex spp.). Ecology 60(4):686–694

    Article  Google Scholar 

Download references

Acknowledgements

We are grateful to two anonymous reviewers for suggestions that improved this manuscript and to Tyler C. Murdock for his assistance at the microbalance. This work was conducted under the U.S. Forest Service permit number APA583, with the support of the National Science Foundation Doctoral Dissertation Improvement Grant, IOS-1311473 and WRT’s National Science Foundation grant, IOS-1021632.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Christina L. Kwapich.

Additional information

Communicated by D. Naug

This manuscript is a contribution to the special issue Integrative Analysis of Division of Labor—Guest Editors: Simon K. Robson, James F. A. Traniello

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kwapich, C.L., Tschinkel, W.R. Limited flexibility and unusual longevity shape forager allocation in the Florida harvester ant (Pogonomyrmex badius). Behav Ecol Sociobiol 70, 221–235 (2016). https://doi.org/10.1007/s00265-015-2039-1

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00265-015-2039-1

Keywords

Navigation