Red imported fire ant
|Red imported fire ant|
Buren, 1972[note 1]
|The original, natural range of S. invicta|
Solenopsis saevissima wagneri Santschi, 1916
The red imported fire ant (Solenopsis invicta), or simply RIFA, is one of over 280 species in the widespread genus Solenopsis. Although the red imported fire ant is native to South America, it has become a pest in the southern United States, Australia, the Caribbean, Taiwan, Hong Kong, the southern Chinese provinces of Guangdong, Guangxi and Fujian, and Macau, RIFAs are known to give a painful, persistently irritating sting that often leaves a pustule on the skin.
- 1 Overview
- 2 Morphology
- 3 Nest social structure
- 4 Behavior
- 5 Monogyny and polygyny
- 6 Economic impact
- 7 Countermeasures
- 8 Genomics
- 9 See also
- 10 Notes
- 11 References
- 12 External links
The red imported fire ant, a eusocial species, are far more aggressive than most ant species. Animals, including humans, often encounter them by inadvertently stepping on one of their mounds, which causes the ants to swarm up the legs, attacking en masse. The ants respond to pheromones released by the first ant that attacks, thereafter stinging in concert.
RIFAs successfully compete against other ants, and have been expanding their range. Recently, colonies of Rasberry crazy ant (also known as Old World crazy ants) have been introduced in the same ranges as RIFAs. These ants are ecologically dominant over fire ants, which has been limiting their range slightly.
They are considered to be a pest, not only because of the physical pain they can inflict, but also because their mound-building activity can damage plant roots, lead to loss of crops, and interfere with mechanical cultivation. It is not uncommon for several fire ant mounds to appear suddenly in a suburban yard or a farmer's field, seemingly overnight. The sting of the RIFA has venom composed of a necrotizing alkaloid, which causes both pain and the formation of white pustules that appear one day after the sting.
Fire ants are excellent natural predators and can be used as biological controls for pests such as sugarcane borers, rice stink bugs, striped earwigs, aphids, boll weevils, soybean loopers, cotton leafworms, hornflies, and many other pests harmful to crops. However, they also kill beneficial pollinators, such as ground-nesting bee species. Seeds, fruits, leaves, roots, bark, nectar, sap, fungi, and carrion are all fire ant food. They are proficient enough at overwhelming intruders, they can virtually clear an area of invertebrates, lizards, and ground-dwelling birds.
Red imported fire ants are extremely resilient, and have adapted to contend with both flooding and drought conditions. If the ants sense increased water levels in their nests, they come together and form a ball or raft that floats, with the workers on the outside and the queen inside. Once the ball hits a tree or other stationary object, the ants swarm onto it and wait for the water levels to recede. To contend with drought conditions, their nest structure includes a network of underground foraging tunnels that extends down to the water table. Also, although they do not hibernate during the winter, colonies can survive temperatures as low as 16 °F (−9 °C).
Red imported fire ants have both a pedicel and postpediole. In other words, they belong to a group of ants that have two humps between the thorax and abdomen. The workers have 10 antennal segments terminating in a two-segmented club. It is often difficult to distinguish between Solenopsis invicta and some other species in the genus. Characteristic differences are not always consistent between the black imported fire ant (Solenopsis richteri) or hybrids between the two species. In fact, positive identifications can often only be made using high performance liquid chromatography to show differences in cuticular hydrocarbons.
Several studies have been conducted on the sex ratios exhibited within colonies of S. invicta. More specifically, the queen was seen to actually control the sex ratios. In an experiment, 24 field colonies were selected with highly biased sex ratios in a monogyne population. Eleven of these colonies were male specialists (numerical proportion of males, range: .77 to 1.0), and 13 were female specialists (numerical proportion of males, range: 0.0 to .09). After exchanging queens, 22 of the 24 colonies accepted the foreign queen, and 21 of these colonies produced a new batch of offspring five weeks later.
Based on the colony from which the queen was originated, the sex ratios of the new colony after the switch could be predicted. For example, after switching, a colony produced predominantly males if the queen came from a male-producing colony, even if the host colony originally produced mainly females. It is not surprising, then, queens that came from a male-favored sex ratio colony produced no significant change in the sex-ratio of another male-favored colony after the switch. The same was true for a queen that came from a female-favored sex ratio colony and switched into another female-favored colony. Therefore, the queen determines the sex ratio, not the workers.
Production of sexuals
Another study compared the inhibition of the number of sexuals (male and female) produced in a single queen colony and a queenless colony. Freshly killed corpses of functional (egg-laying) queens were added daily to queenless colonies. These effectively inhibited the production of sexuals through the excretion of pheromones, although not as effectively as living queens. Conversely, corpses of queens not laying eggs did not inhibit the production of sexuals when added to queenless colonies. Also, when queens were introduced into queenless colonies that already had developed sexual larvae, workers in the colony executed these larvae. This indicates the queen’s control over the production of sexuals can be enforced retroactively, even after the larvae are sexualized. These results provide evidence that functional queens exert control over the production of sexuals in S. invicta through pheromones that influence the behaviors of workers toward both male and female larvae.
S. invicta also presents a paradox for kin selection theory. In multiple-queen (polygyne) colonies, the egg-laying queens are, on average, unrelated to one another, so the workers appear to raise new sexuals that are no more closely related to them than are random individuals in a population. This was tested by removing worker/queen pairs engaged in trophallaxis with forceps, and then sampling the allele frequency to estimate for the reference population. Frequencies of the most common allele at each locus have been found to conform to Hardy-Weinberg expectations in past studies. Genotypic data were used to estimate relatedness between the workers and the winged-queens they tended, and it was virtually zero. The results indicate S. invicta workers tending queens in polygyne nests do so without respect to the relatedness of those queens.
Unrelated queens commonly found a colony cooperatively. This joint effort of the cofoundresses contributes to the growth and survival of the incipient colony. However, such associations are not always stable. The emergence of the first workers instigates queen-queen and queen-worker fighting. The two factors that could affect the survival of individual queens are their relative fighting capabilities and their relative contribution to worker production. Experimentation indicates that size, an indicator of fighting capacity, positively correlates with survival rates. However, manipulation of the queen’s relative contribution to worker production had no correlation with survival rate. It can be assumed that the worker brood cannot favor its mother based on these results.
S. invicta workers not only tend to queens indiscriminately, but they also indiscriminately attack them. Queens producing diploid males reared fewer offspring, but were as likely to survive as queens producing only workers. It would have been assumed that if workers controlled queen mortality, they would be expected to discriminate in favor of their mother, therefore increasing their inclusive fitness. This, however, should favor the queen with the greatest number of daughters during the period of queen execution. The data actually show the fights among queens themselves have a strong role in determining which queen survives—the heavier cofoundress was more likely to win. Thus, queen survival is enhanced by high fighting ability relative to cofoundresses, rather than by the number of offspring she has. Workers respond to these queen differences by attacking the previously injured queen to reinforce the effects of competition among the queens.
Necrophoric behavior refers to the disposal of corpses. In many species of ants, workers discard uneaten food and other such wastes in a refuse pile. Pioneering work was undertaken by Wilson (1958), who studied the impetus behind corpse disposal in worker ants, Pogonomyrmex badius Latreille. Filter paper squares treated with acetone extracts of P. badius corpses were carried to the refuse pile in the same manner as corpses. The active component was not identified, but the fatty acids accumulating as a result of decomposition were implicated and bits of paper coated with synthetic oleic acid typically elicited a necrophoric response. The process behind this behavior in imported red fire ants was confirmed by Blum (1970): unsaturated fats, such as oleic acid, elicit corpse removal behavior. Freshly frozen RIFA workers were not treated like corpses by their nest mates and were not carried away since there was no decomposition and therefore no accumulation of fatty acids. Furthermore, after healthy workers received a light application of oleic acid and were returned to their nest, workers encountering the treated ants quickly seized them and transported them to the refuse pile.
Social factors can affect an animal’s response to a chemical cue. Gordon, examining the effect of social context on the response of ant colonies to oleic acid, found that colonies responded to oleic acid differently in different social contexts, carrying objects to the midden only in certain situations. When a large majority of ants (greater than 15%) are doing midden work or nest maintenance, treated objects were taken to the midden. However, if the majority of the ants were foraging or convening, treated objects were taken to the nest. The colonies respond to oleic acid by quickly relocating the treated object to destinations that are appropriate for their current activities. If a plurality of the colony’s work force is participating in an activity, a worker encountering the treated paper likely is engaging in that activity. Thus, if most ants are participating in midden work, the paper encountered by a midden worker likely will be carried to the midden. However, if a large percentage of the ants outside the nest are feeding or are part of a group being recruited to a food source, a forager will probably discover the treated object and carry it into the nest as food. The response to oleic acid depends on colony activities at the time treated objects are encountered.
Polygynous colonies differ substantially from monogynous colonies in social insects. The former experience reductions in queen fecundity, dispersal, longevity, and nestmate relatedness. Understanding the mechanisms behind queen recruitment is integral to understanding how these differences in fitness are formed. It is unusual that the number of older queens in the colony does not influence new queen recruitment. Levels of queen pheromone, which appears to be related to queen number, play important roles in regulation of reproduction. It would follow that workers would reject new queens when exposed to large quantities of this queen pheromone. Moreover, experimental data support the claim that queens in both populations enter nests at random, without any regard for the number of older queens present. There is no correlation between the number of older queens and the number of newly recruited queens. Three hypotheses have been posited to explain the acceptance of multiple queens into established colonies: mutualism, kin selection, and parasitism. The mutualism hypothesis states that cooperation leads to an increase in the personal fitness of older queens. However, this hypothesis is not consistent with the fact that increasing queen number decreases both queen production and queen longevity. Kin selection also seems unlikely given that queens have been observed to cooperate under circumstances where the queens are statistically unrelated. Therefore, queens experience no gain in personal fitness by allowing new queens into the colony. Parasitism of preexisting nests appears to be the best explanation of polygyny. One theory is that so many queens attempt to enter the colony that the workers get confused and inadvertently allow several queens to join the colony.
Monogyny and polygyny
Recognition between conspecifics is an essential attribute of ant social behavior for repelling non-nestmates and protecting food resources. RIFAs use olfactory cues produced by queens to discriminate between colony members and conspecific intruders. They also use environmentally derived cues to discriminate between colony members and nonmembers. RIFAs have two distinct forms of colony organization: monogyny and polygyny, distinguishable by the number of reproductive queens, how reproduction is divided among members of the colony, the number of individuals produced, the degree of genetic relatedness, and queens' and workers' behaviors. Different behaviors are correlated with allelic differences at the nuclear gene general protein-9 (Gp-9) that codes for two groups of odor-binding proteins. Queens of monogyne colonies possess B-like alleles (with BB genotype) and are more prolific, heavier, and longer-lived than queens of polygyne colonies. In Argentina, polygyne colonies can be heterozygous (Bb) or homozygous (BB), thus some polygyne workers present b-like alleles.
Behavioral discrimination between conspecifics
Monogyne workers kill foreign queens and aggressively defend their territory. However, not all behaviors are universal, primarily because worker behaviors depend on the ecological context in which they develop, and the manipulation of worker genotypes can elicit change in behaviors. Therefore, behaviors of native populations can differ from those of introduced populations. In a study to assess the aggressive behavior of monogyne and polygyne red fire ant workers by studying interaction in neutral arenas, and to develop a reliable ethogram for readily distinguishing between monogyne and polygyne colonies of RIFAs in the field, monogyne and polygyne workers discriminated between nestmates and foreigners as indicated by different behaviors ranging from tolerance to aggression. Monogyne ants always attacked foreign ants independently if they were from monogyne or polygyne colonies, whereas polygyne ants recognized, but did not attack, foreign polygyne ants, mainly by exhibiting postures similar to behaviors assumed after attacks by Pseudacteon phorids. Hostile versus warning behaviors were strongly dependent on the social structure of workers. Therefore, the behavior toward foreign workers was a reliable ethological indicator to characterize monogyne and polygyne colonies of RIFAs.
The monogynous red imported fire ant colony’s territorial area and the mound size are positively correlated, which, in turn, is regulated by the colony’s size (number and biomass of workers), distance from neighboring colonies, prey density, and by the colony's collective competitive ability. In contrast, nestmate discrimination among polygynous colonies is more relaxed as workers tolerate conspecific ants alien to the colony, accept other heterozygote queens, and do not aggressively protect their territory from polygyne conspecifics. These colonies might increase their reproductive output as a result of having many queens and the possibility of exploiting greater territories by means of cooperative recruitment and interconnected mounds. Therefore, polygyne workers displayed low aggressive responses toward polygyne non-nestmates because lower aggression results in higher survival. Consequently, the behavior of workers is another reliable factor to characterize both monogyne and polygyne colonies of red imported fire ant, in addition to considering mean worker sizes, density or distance between mounds, number of queens, or molecular assays.
An outbreak of the RIFAs in Queensland, Australia, was discovered on 22 February 2001. The ants were believed to be present in shipping containers arriving at the Port of Brisbane from the United States. Anecdotal evidence suggests fire ants may have been present in Australia for six to eight years prior to formal identification. While the outbreak is restricted to a small (800-km2) region of southeast Queensland in and around Brisbane, the potential social, economic, and ecological damage prompted the Australian government to respond rapidly. The initial emergency response was followed by the formation of the Fire Ant Control Centre in September 2001. Joint state and federal funding of A$175 million was granted for a six-year eradication program involving the employment of more than 600 staff and the broad-scale baiting of about 678.9 km2 between eight and 12 times, followed by two years of surveillance. Following the completion of the fourth year of the eradication program, the Fire Ant Control Centre estimated eradication rates of greater than 99% from previously infested properties. The federal budget confirmed the program will receive extended Commonwealth funding of around A$10 million for at least another two years, until June 2009, to treat the residual infestations found most recently, and to fund validation of the overall treatment and surveillance program. As in previous years, the states have agreed in principle to match the federal funding. That decision is set to be ratified in June 2007.[dated info]
Reports from the Philippines, however, have not been confirmed and are likely to be misidentification of the tropical fire ant (Solenopsis geminata).
The Food and Drug Administration (FDA) estimates more than US$5 billion are spent annually on medical treatment, damage, and control in RIFA-infested areas. Further, the ants cause about US$750 million in damage to agricultural assets, including veterinary bills and livestock loss, as well as crop loss.
Many scientists and agencies are attempting to develop methods to stop the spread of the RIFA. Typically, control has been achieved through pesticide use. From the 1950s into the 1970s, Mirex was extensively used in an attempt to eradicate the species. However, the pesticide inadvertently aided the fire ants' spread by killing numerous native ant species that compete successfully with them. Mirex also caused even broader ecological harm that was often attributed to the fire ants. For example, it was first thought that the ants were linked to the decline of overwintering birds (e.g. the loggerhead shrike), but a later study showed the pesticides were largely to blame. RIFAs have virtually no natural biological control agents native to, or naturalized in, the United States, China, the Philippines, or Australia. Current research is focused on introducing biological control agents from the RIFA's native range.
The microsporidian protozoan Thelohania solenopsae and the fungus Beauveria bassiana are promising pathogens. Solenopsis daguerrei, a parasitic ant, invades RIFA colonies to replace the queen in hopes of gaining control of the colony. For this reason, its use as a biological control agent is also being explored.
Pseudacteon tricuspis and Pseudacteon curvatus are parasitoid phorid flies from South America which parasitize the ants. The female flies each lay an egg at the junction of head and thorax of their victims, prompting a jerky dance manoeuvre by the ants. The larva then slowly consumes the contents of the head, decapitating the ant in the process, and uses the exoskeleton as a pupal case.
Phorid flies have been introduced in many places in southeastern United States, and are slowly reproducing and spreading to cover the entire RIFA range. The amount of actual damage done to the ants by phorid flies is minimal, but the ants appear to be aware of the hovering flies, losing their social organization and ceasing foraging. In addition, phorid flies are very species-specific, and should, in theory, leave native ant species (the fire ants' prime competitors) unmolested.
Scientists at the US Agricultural Research Service also have been able to infect phorid flies with Kneallhazia solenopsae, a spore-producing insect pathogen, to control the population of RIFAs. The flies are unharmed by the pathogen and serve as vectors in transmitting the disease to the ants. The pathogen is able to reduce colonies by 53-100%, and may serve as an effective biological control for the ants.
A virus, SINV-1, has been found in about 20% of fire ant fields, where it appears to cause the slow death of infected colonies. It has proven to be self-sustaining and transmissible. Once introduced, it can eliminate a colony within three months. Researchers believe the virus has potential as a viable biopesticide to control fire ants.
In some cases, hastily adopted biological control agents can do more harm than good (such as the western mosquitofish in Australia), and it remains to be seen how much success biological control of the RIFA will have.
Researchers have also been experimenting with extreme temperature change to exterminate RIFAs, such as injecting liquid nitrogen or pressurized steam into RIFA nests. Besides using hot steam, pouring boiling water into ant mounds has been found effective in exterminating their nests. Folk remedies have often sought a rapid increase in temperature by soaking the nest in gasoline or kerosene and lighting it on fire, though this is potentially dangerous. Further, the burning of the nest is ineffective due the tendency of queens to be several feet underground. This confusion stems from the observation that fuel vapor has a near instantaneous lethal effect on the ants.
In Brisbane, Australia, colonies are being eradicated or effectively controlled by ground baiting with food laced with contraceptives that render the colony's queen infertile, and toxicants. Mass baiting was undertaken following detection of the ants around the port of Brisbane and in southwestern Brisbane in 2001. Widespread public reporting of suspect colonies (by sending in samples of ants for identification) allowed mapping of the ant's locations. This was combined with satellite imagery to determine the vegetated habitats most likely to be infiltrated by the ants, and the baits were targeted in these areas. Known infested areas were declared high-risk restricted areas, and any material being moved from these areas which could harbour ants (soil, mulch, potted plants, potting mix, hay bales, construction machinery, etc.) had to be inspected prior to disposal or movement, and bulk waste sent to transfer stations for examination, treatment, and disposal. The infestation was initially thought to cover 270 km2, with a density of up to 600,000 colonies/km2 on highly infested sites. As program activity refined data on the infested area, overall size grew to around 80,000 ha by 2006/7. At mid-2007 in the ongoing nationally funded eradication campaign, fewer than 100 active colonies were located in the entire South-East Queensland area between September 2006 and February 2007. The focus of delivering eradication has now switched largely to surveillance, while control and validation measures are expected to continue until 2009. The six-year eradication campaign has cost A$175 million to date, and had secured funding in principle for a minimum of two more years.
A fire ant genome was sequenced in 2010. This creates new opportunities for research on fire ant behavior, and offers new opportunities for directed control measures that minimize environmental impact. The sequence can be searched and downloaded at antgenomes.org.
- The species was first described as Solenopsis saevissima wagneri (a variety of Solenopsis saevissima) by Santschi (1916). Creighton (1930) reclassified the taxon as Solenopsis saevissima electra var. wagneri (infrasubspecific); Wilson (1952) placed the taxon as a junior synonym of S. saevissima saevissima. In 1972, Buren described what he thought was a new species, Solenopsis invicta. Trager (1991) synonymized both taxa; incorrectly citing Solenopsis saevissima electra wagneri as the original name, he erroneously believed that the name Solenopsis wagneri was unavailable, and used Buren's name Solenopsis invicta. To avoid confusion, ICZN decided to conserve the now widely used name Solenopsis invicta, despite that Solenopsis wagneri had priority.
- Shattuck, S. O.; Porter, S. D.; Wojcik, D. P. (1999). "Case 3069. Solenopsis invicta Buren, 1972 (Insecta, Hymenoptera): proposed conservation of the specific name.". Bulletin of Zoological Nomenclature 56 (1): 27–30.
- M. S. Ascunce et al., “Global Invasion History of the Fire Ant Solenopsis invicta”, Science, vol. 331, no. 6020, pp. 1066 - 1068, 2011. - See more at: http://www.sciencemag.org/content/331/6020/1066.short
- Z. Ling, L. YongYue, H. XiaoFang, Z. WeiQiu, and L. GuangWen, “Identification of red imported fire ant, Solenopsis invicta, to invade mainland China and infestation in Wuchuan, Guangdong”, Chinese Bulletin of Entomology, vol. 42, pp. 144–148, 2005.
- "Red imported fire ant, Solenopsis invicta Buren". UF/IFAS Featured Creatures.
- Oppenheimer, Daniel; LeBrun, Edward G. (May 16, 2013). "Invasive Crazy Ants Are Displacing Fire Ants, Researchers Find". University of Texas, Austin.
- Flatow, Ira (April 29, 2011). Bug News Roundup: Ant Rafts, Robot Caterpillars (video) Science Friday. NPR. Retrieved 9 May 2011.
- Mlot, Nathan J.; Craig A. Tovey; David L. Hu (April 25, 2011). "Fire ants self-assemble into waterproof rafts to survive floods". Proceedings of the National Academy of Sciences. doi:10.1073/pnas.1016658108. Retrieved 9 May 2011.
- Keller, Laurent; Ross, Kenneth G. (1998). "Selfish genes: a green beard in the red fire ant" (PDF). Nature 394 (6693): 573–575. doi:10.1038/29064.
- Passera, Luc, S. Aron, E.L. Vargo, and L. Keller. "Queen Control of Sex Ratio in Fire Ants." Sciencemag (2001): 1308
- Davies, N.B., Krebs, J.R., and West, S.A. An Introduction to Behavioural Ecology. 4th ed. West Sussex: Wiley-Blackwell, 2012. Pg. 385.
- Vargo, E.L., Fletcher, David J.C. "Evidence of pheromonal queen control over the production of male and female sexuals in the fire ant, Solenopsis invicta" Journal of Comparative Physiology A. Volume 159, Issue 6, pp. 741-749.
- DeHeer, C.J. and Ross, K.G. "Lack of Detectable Nepotism in Multiple-Queen Colonies of the Fire Ant Solenopsis invicta (Hymenoptera: Formicidae)." Behavior Ecology and Sociobiology. Volume 40, Number 1 (1997), pp 27-33.
- Goodisman, Michael; Ross (1999). Queen recruitment in a multiple-queen population of the fire ant Solenopsis invicta. Behavioral Ecology. Retrieved 25 August 2014.
- Bernasconi, G.; Keller, L. (22 April 1996). "Reproductive Conflicts in Cooperative Associations of Fire Ant Queens (Solenopsis invicta)". Proceedings of the Royal Society B: Biological Sciences 263 (1369): 509–513. doi:10.1098/rspb.1996.0077. Retrieved 14 November 2014.
- Balas, M.T., Adams, E.S. "The dissolution of cooperative groups: mechanisms of queen mortality in incipient fire ant colonies." Behavioral Ecology and Sociobiology. Volume 38, Number 6 (1996). pp 391-399.
- Maeterlinck, Maurice (1930). The Life Of The Ant. London Toronto Melbourne and Sydney Cassell and Company Ltd. Retrieved 25 August 2014.
- Howard, Dennis F.; Tschinkel, Walter R. (1976). Aspects of Necrophoric Behavior in the Red Imported Fire Ant, Solenopsis invicta. BRILL. p. 157-180. Retrieved 25 August 2014.
- Wilson, E.O.; Durlach, N.I.; Roth, L.M. (1958). Chemical Releasers of Necrophoric Behavior in Ants. Psyche. p. 65:108-114. Retrieved 25 August 2014.
- Gordon, Deborah M. (1983). Dependence of necrophoric response to oleic acid on social context in the ant,Pogonomyrmex badius. Journal of Chemical Ecology. p. 105-111. Retrieved 25 August 2014.
- Wilson, Edward O. (1962). Chemical communication among workers of the fire ant Solenopsis saevissima (Fr. Smith) 3. The experimental induction of social responses. Cambridge, Massachusetts, USA: Biological Laboratories, Harvard Universit. p. 159-164. Retrieved 25 August 2014.
- Goodisman, Michael; Ross, Kenneth (1998). A Test of Queen Recruitment Models Using Nuclear and Mitochondrial Markers in the Fire Ant Solenopsis invicta. Society for the Study of Evolution. Retrieved 25 August 2014.
- Harrison, Richard G. (1980). Dispersal Polymorphisms in Insects. Annual Reviews. p. 95-118. Retrieved 25 August 2014.
- DeHeer, Christopher; Goodisman, Michael; Ross, Kenneth (1999). Queen Dispersal Strategies in the Multiple‐Queen Form of the Fire Ant Solenopsis invicta.. The University of Chicago Press. p. 660-675. Retrieved 25 August 2014.
- Keller, Laurent (1995). Social life: the paradox of multiple-queen colonies. University of Lausanne. p. 355-360. Retrieved 25 August 2014.
- Ross, Kenneth (1993). The Breeding System of the Fire Ant Solenopsis invicta: Effects on Colony Genetic Structure. The University of Chicago Press. p. 554-576. Retrieved 25 August 2014.
- Goodisman, Michael; Sankovich, Karen; Kovacs, Jennifer (2007). Genetic and morphological variation over space and time in the invasive fire ant Solenopsis invicta. Biological Invasions. p. 571-584. Retrieved 25 August 2014.
- Adams, Eldridge; Balas, Michael (1999). Worker discrimination among queens in newly founded colonies of the fire ant Solenopsis invicta. Behavioral Ecology and Sociobiology. p. 330-338. Retrieved 25 August 2014.
- “Behavioral Discrimination Between Monogyne and Polygyne Red Fire Ants (Hymenoptera: Formicidae) in Their Native Range."
- Relationship of queen number and queen relatedness in multiple-queen colonies of the fire ant Solenopsis invicta
- Mechanisms of population regulation in the fire ant Solenopsis invicta: an experimental study. Journal of Animal Ecology
- Wetterer, James K. (2013). "Exotic spread of Solenopsis invicta (Hymenoptera: Formicidae) beyond North America". Sociobiology 60: 53–63.
- McDonald, Maggie (February 2006). "Reds Under Your Feet (interview with Robert Vander Meer)". New Scientist 189 (2538): 50.
- Theodoropoulos, D. 2003. Invasion Biology. Avaar Books, Blythe, CA
- Yosef, R and FE Lohrer. 1995. Loggerhead shrikes, fire ants and red herrings? Condor 97:1053-1056
- Durham, Shannon (2010). "ARS Parasite Collections Assist Research and Diagnoses". Agricultural Research Service. United States Department of Agriculture. Retrieved 25 August 2014.
- "ARS Parasite Collections Assist Research and Diagnoses". USDA Agricultural Research Service. January 28, 2010.
- Steven M. Vallesa, Charles A. Strong, Phat M. Dang, Wayne B. Hunter, Roberto M. Pereira, David H. Oi, Alexandra M. Shapiro, David F. Williams (2004-07-09). "A picorna-like virus from the red imported fire ant, Solenopsis invicta: initial discovery, genome sequence, and characterization". Virology 328 (1): 151–157. doi:10.1016/j.virol.2004.07.016. PMID 15380366.
- "Integrated management of imported fire ants and emerging urban pest problems". United States Department of Agriculture. May 17, 2007.
- "Fire ants may have met their match". CNN. May 7, 2007. Archived from the original on May 13, 2007.
- Nature & Science » Biology Resources » Integrated Pest Management Manual
- Catalyst: Fire Ant update - ABC TV Science
- Wurm, Yannick. "The genome of the fire ant Solenopsis invicta". National Academy of Sciences of the United States of America. Retrieved 25 August 2014.
|Wikimedia Commons has media related to Solenopsis invicta.|
- The Incredible Floating Fire Ant
- Red Imported Fire Ant Fact Sheet on fire ant control, infestations and prevention from the National Pest Management Association
- Imported Fire Ants: Biology, Control, and Management at eXtension
- Database of fire ant genes
- Fire ants page at the Department of Primary Industries & Fisheries, Queensland