Translator Disclaimer
1 September 2013 No Enemies Needed: Cotton Aphids (Hemiptera: Aphididae) Directly Benefit from Red Imported Fire Ant (Hymenoptera: Formicidae) Tending
Author Affiliations +

Honeydew is a carbohydrate-rich solution excreted by phloem-feeding insects such as aphids. Ants often consume this substance and, in return, protect aphids from natural enemies. This indirect benefit of ant-aphid mutualisms to aphids (reduced predation) has been examined extensively. Few studies, however, have quantified the direct benefits that aphids may gain from the mutualism. We conducted greenhouse experiments to estimate the direct benefits that cotton aphids, Aphis gossypii (Glover) (Hemiptera: Aphididae), receive from their mutualistic relationship with red imported fire ants, Solenopsis invicta (Buren) (Hymenoptera: Formicidae). We compared population growth and alate production between ant-tended and untended aphid colonies in the absence of natural enemies. We found strong evidence that cotton aphids receive direct benefits from their relationship with fire ants. After 12 days, aphid colonies with tending ants were 46% larger than their non-tended counterparts. Alate production, however, was not affected by ant tending, suggesting that a reduction in dispersal did not explain the ant effect on aphid population growth. We hypothesize that the increase in aphid population size results from altered feeding behaviors in the presence of ants. This study suggests that there may be constant selection for this mutualism even in the absence of aphid natural enemies because aphids gain direct benefits.

Numerous studies have examined mutualistic interactions between ants and aphids. Ants consume honeydew, a carbohydrate-rich solution excreted by aphids, and in return protect aphids from natural enemies (Way 1963). Few studies, however, have quantified the potential direct benefits aphids receive from tending ants. Direct benefits would provide continuous selection for honeydew-producing insects to form relationships with tending ants and may explain why these relationships are ubiquitous in nature.

Tending ants may directly affect aphid population growth through several mechanisms. Ants can reduce aphid dispersal by reducing the number of alate (winged) individuals within a population. Previous studies intriguingly suggest that ants chemically inhibit aphid wing formation (Kleinjan & Mittler 1975) whereas others suggest ants physically remove wings from alate individuals (Kunkel 1973). A reduction in alates could increase aphid populations by reducing dispersal. The presence of ants may also affect aphid longevity and fecundity. For instance, Flatt & Weisser (2000) observed that when aphid predators were excluded, individual aphids (Metopeurum fuscoviride Stroyan) lived significantly longer and matured faster when tended by the black garden ant, Lasius niger L. Furthermore, tended aphids produced on average 63 more offspring than unattended aphids. In addition, ant tending may allow aphids to feed at optimal rates due to reduced aphid predator abundance. Increased feeding efficiency can increase resources allocated towards reproduction thereby increasing population growth (Slansky & Scriber 1985). However, Stadler & Dixon (1998) observed black bean aphids, Aphis fabae (Scopoli), experience adverse effects when tended by Lasius niger. Aphids experienced reductions in growth rates and gonad size when tended by ants suggesting increased feeding rates reduce the efficiency of nutrient assimilation.

Lastly, aphids may receive hygienic benefits from honeydew removal by ants. Excessive honeydew accumulation can result in pathogens such as sooty mold. Sooty mold, a fungus that grows on honeydew, creates a black layer on the upper side of leaves, thereby decreasing photosynthesis and causing leaf abscission (Wood et al. 1988). Sooty mold growth can negatively impact herbivores, including aphids, by reducing host plant quality (Way 1963, Wood et al. 1988). Therefore honeydew removal by ants may benefit aphids by reducing fungal infections and maintaining host plant quality.

Cotton aphids (Aphis gossypii) (Glover) are pests of several agricultural crops including cotton (Gossypium hirsutum L.) cucurbits, okra (Abelmoschus esculentus L.), and tomato (Lycopersicon esculentum) (Miller) (Ebert & Cartwright 1997). Aphid infestations in cotton reduce boll weight (Fuchs & Minzenmayer 1995) and honeydew accumulation can result in additional economic damage by contaminating and reducing the quality of cotton lint (Carter 1992). The red imported fire ant (Solenopsis invicta) (Buren) was unintentionally introduced to North America approximately 80 years ago and has spread to at least 15 states. Several studies have quantified the indirect benefits that aphids receive as a result of fire ant protection from natural enemies (e.g., Kaplan & Eubanks 2002, 2005). This study used greenhouse experiments to examine the direct benefits that cotton aphids potentially receive from their mutualistic relationship with fire ants in the absence of natural enemies.


To examine the direct effects of ants on aphid population growth and alate production greenhouse experiments were conducted on the campus of Auburn University, Auburn, Alabama, during July 2005. Fifty-six cages (75 × 30 × 30 cm) were constructed from PVC pipe framing and mesh mosquito netting and placed around a 37 liter plastic container filled with potting soil. A cotton plant with 5–6 true leaves (∼1 m tall) was placed in each cage. One-hundred apterous cotton aphids of similar coloration and size were transferred from a greenhouse colony to each caged plant and allowed to acclimate for 24 hrs. Field collected fire ant colonies (∼500 ants) were added to half (28) of the cages. The inside and outside rim of plastic containers were lined with liquid polytetrafluoroethylene (Teflon®) to exclude ants from entering ant absent treatments and escaping from ant treatments. Ants immediately began tending aphids and consuming honeydew. Starting 5 days after experimental setup and every other day thereafter the upper and lower surface of each leaf, branch, and stem was surveyed and the total number of apterous and alate aphids on each plant recorded. Repeated measures ANOVA (Proc GLM; all statistical analyses were performed using SAS, Version 9.1 [SAS Institute 2002]) was conducted to compare aphid colony growth and alate production.


We found strong evidence that cotton aphids receive additional direct benefits from their mutualistic relationship with fire ants in the absence of natural enemies. After 7 days, aphid colonies tended by ants were 35% larger than unattended colonies (F3,158 = 2.02, P = 0.0455). This trend continued throughout the remainder of the experiment and by day 12, aphid colonies with ants were 46% larger than aphid colonies without ants (F3,158 = 7.19, P < 0.0001) (Fig. 1). No apterous aphid dispersal was observed throughout the experiment. Alate abundance remained low in both treatments throughout the entire experiment and no significance difference was observed between ant tended and untended aphids on any sampling date. At the conclusion of the study ant tended aphids averaged 8.87 alates per colony compared with 9.03 alates in untended colonies (F3,158 = 0.08, P = 0.9402).

Fig. 1.

The direct effects of fire ants on cotton aphid population size (means ± SE) in the absence of natural enemies. An asterisk indicates means were significantly different on sampling dates at the P = 0.05 level.



Tending ants may alter aphid behavior resulting in increased colony growth. For instance, aphid phloem consumption rate depends on duration and frequency of feeding probes (Risebrow & Dixon 1987) and aphids have the ability to alter their feeding rates (Dixon 1963). Additionally, ant tending may signal a reduction in predation risk to aphids, resulting in decreased antipredatory behaviors. Tending ants may encourage aphids to feed continuously, thereby increasing feeding efficiency (Rauch et al. 2002) leading to increased resource uptake and higher reproduction rates. Although few studies have examined this, some evidence does suggest that ant tending affects aphid feeding rates. Banks & Nixon (1958) observed increased honeydew production from tended ants and concluded that ants stimulate aphid feeding. Likewise, Brenton & Addicott (1992) suggest, Aphis variens (Patch), increases its feeding rate when tended by the ant Formica cinera (Wheeler). Further, aphids often respond to predators or alarm pheromones by dropping from host plants (Losey & Denno 1998). Dropping from host plants can increase individual aphid survival but can decrease population growth due to lost foraging opportunities (Fill et al. 2012). Costly antipredator behaviors; however, can not explain the results of our study because aphid natural enemies were completely excluded from the aphid colonies.

In addition to reduced antipredatory behavior, honeydew removal by ants likely provides an important hygienic service to aphids. Honeydew accumulation can increase the incidence of pathogens, such as sooty mold, and decrease host plant quality by reducing available photosynthetic leaf area. Bach (1991) observed reduced honeydew and sooty mold accumulation on plants with ants compared with plants without ants. When ants were excluded, 89.5% of leaves contained honeydew; whereas only 6% contained honeydew when ants were present. Additionally, the presence of ants reduced sooty mold growth by 20% in this study. In the absence of ants, Fokkema et al. (1983) observed a tenfold increase in fungal pathogens, such as sooty mold, due to excessive honeydew build up. However due to the short experimental duration and low aphid densities, we observed no evidence of sooty mold contamination in either treatment.

The presence of ants had no effect on aphid alate production. In fact, alate production was very low in both treatments. Previous studies suggest a reduction in alates when ants tend aphids (Kleinjan & Mittler 1975; Tilles & Wood 1982). However, alate production is also inversely correlated with host plant quality (Dixon 1998). Plants in our experiment were healthy and lacked other herbivores. Therefore aphids may not have produced alates regardless of the presence or absence of ants due to the high quality of host plants used in this experiment.

This study is one of the first to document direct benefits to aphids from ant tending. In addition to the indirect benefits provided by ants (protection from natural enemies), aphids receive direct benefits such as increased population growth when fire ants were present. These additional direct benefits likely increase selection pressure for this mutualistic relationship. Future studies quantifying costs and benefits of mutualistic interactions should evaluate direct as well as indirect benefits. Additional studies should also attempt to elucidate the exact mechanisms underlying the direct benefits aphids receive from tending ants.


We thank John Styrsky, Joel Tindle, Mike Buckman and Laura Cooper for laboratory assistance. We thank Henry Fadamiro and John Murphy for helpful comments on an earlier draft. This work was supported by an Auburn University Biogrant and the Alabama Fire Ant Management Program.



C. E. Bach 1991. Direct and indirect interactions between ants (Pheidole megaphala), scales (Coccus viridis) and plants (Pluchea indica). Oecologia 87: 233–239. Google Scholar


C. J. Banks , and H. L. Nixon . 1958. Effects of the ant Lasius niger L., on the feeding and excretion of the bean aphid, Aphis fabae Scop. Exp. Biol. 35: 703–711. Google Scholar


L. M. Breton , and J. E. Addicott . 1992. Densitydependent mutualism in an aphid-ant interaction. Ecology 73: 2175–2180. Google Scholar


F. L. Carter 1992. The sticky cotton issue, p. 645 In Proc. Beltwide Cotton Conference, National Cotton Council of America, 6–10 Jan 1992, Memphis, TN. Google Scholar


A. F. G. Dixon 1963. Reproductive activity of the sycamore aphid, Drepanosiphum plantanoides (Schr.) (Hemiptera, Aphididae). J. Anim. Ecol. 32: 33–48. Google Scholar


A. F. G. Dixon 1998. Aphid Ecology. Chapman and Hall. London. Google Scholar


T. A. Ebert , and B. Cartwright 1997. Biology and ecology of Aphis gossypi Glover (Hemiptera: Aphididae). Southwest. Entomol. 22: 116–153. Google Scholar


A. Fill , E. Y. Long , and D. L. Finke 2012. Non-consumptive effects of a natural enemy on a non-prey herbivore population. Ecol. Entomol. 37: 43–50. Google Scholar


T. Flatt , and W. W. Weisser 2000. The effects of mutualistic ants on aphid life history traits. Ecology 81: 3522–3529. Google Scholar


N. J. Fokkema , I. Riphagen , R. J. Poot , and C. DeJong 1983. Aphid honeydew, a potential stimulant of Cochliobolus sativus and Septoria nodorum and the competitive role of saprophytic mycoflora. Trans. British Mycol. Soc. 81: 355–368. Google Scholar


T. W. Fuchs , and R. Minzenmayer 1995. Effects of Aphis gossypii on cotton development and yield in west Texas. Southwest. Entomol. 20: 341–349. Google Scholar


I. Kaplan , and M. D. Eubanks 2002. Disruption of cotton aphid (Homoptera: Aphididae)-natural enemy dynamics by red imported fire ants (Hymenoptera: Formicidae). Environ. Entomol. 31: 1175–1183. Google Scholar


I. Kaplan , and M. D. Eubanks 2005. Aphids alter the community-wide impact of fire ants. Ecology 86: 1640–1649. Google Scholar


J. E. Kleinjan , and T. E. Mittler 1975. A chemical influence of ants on wing development in aphids. Entomol. Exp. Appl. 18: 384–388. Google Scholar


H. Kunkel 1973. Die Kotagabe der Aphiden (Aphidina, Hemiptera) unter Einfluss von Ameisen. Bonn Zool. Beitr. 24: 105–121. Google Scholar


J. E. Losey , and R. F. Denno 1998. The escape response of pea aphids to foliar-foraging predators: factors affecting dropping behavior. Ecol. Entomol. 23: 53–61. Google Scholar


G. Rauch , J. C. Simon , B. Chaubet , L. Haack , T. Flatt , and W. W. Weisser 2002. The influence of ant attendance on aphid behavior investigated with the electrical Penetration graph technique. Entomol. Exp. Appl. 102: 13–20. Google Scholar


A. Risebrow , and A. F. G. Dixon 1987. Nutritional ecology of phloem-feeding insects, pp. 421–448. In F. Slansky , and J.G. Rodriquez [eds.], Nutritional Ecology of Insects, Mites, Spiders, and Related Arthropods, New York: Wiley and Sons. Google Scholar


SAS INSTITUTE. 2002. SAS statistical software. Version 9.1. SAS Institute, Cary, North Carolina, USA. Google Scholar


F. Slansky Jr. , and J. M. Scriber 1985. Food consumption and utilization, pp. 87–163 In G. A. Kerkut and L. I. Gilbert [eds.], Comprehensive Insect Physiology, Biochemistry, and Pharmacology, Pergamon Press, Oxford. Google Scholar


B. Stadler , and A. F. G. Dixon 1988. Costs of ant attendance for aphids. J. Animal Ecol.67: 454–459. Google Scholar


D. A. Tilles , and D. L. Wood 1982. The influence of carpenter ant (Camponotus modoc) (Hymenoptera: Formicidae) attendance on the development and survival of aphids (Cinara Spp.) (Homoptera: Aphididae) in a giant Sequoia forest. Canadian Entomol. 114: 1133–1142. Google Scholar


M. J. Way 1963. Mutualisms between ants and honeydew producing Homoptera. Annu. Rev. Entomol. 8:307–344. Google Scholar


B. W. Wood , W. L. Tedders , and C. C. Reilly 1988. Sooty mold fungus on pecan foliage suppresses light penetration and net photosynthesis. HortScience 23: 851–853. Google Scholar
Kevin B. Rice and Micky D. Eubanks "No Enemies Needed: Cotton Aphids (Hemiptera: Aphididae) Directly Benefit from Red Imported Fire Ant (Hymenoptera: Formicidae) Tending," Florida Entomologist 96(3), 929-932, (1 September 2013).
Published: 1 September 2013

Back to Top