Polyergus breviceps

Polyergus breviceps

Taxobox
name = "Polyergus breviceps"


status = VU | status_system = IUCN2.3
regnum = Animalia
phylum = Arthropoda
classis = Insecta
ordo = Hymenoptera
familia = Formicidae
genus = "Polyergus"
species = "P. breviceps"
binomial = "Polyergus breviceps"
binomial_authority = (Emery, 1893)
synonyms =

Introduction

"Polyergus breviceps" is a species of insect in family Formicidae. It is endemic to the United States†. It is a social parasite of other ants, namely of Formica gnava but also of Formica occulta. Polyergus is an inquiline parasite, having lost its ability to take care of its young and themselves. “The workers do not forage for food, feed the young or the queen, or even clean up their own nest” (Topoff 1999). In order to survive, Polyergus workers raid Formica nest for their pupae that, once hatched, become workers of the mixed nest. This sort of relationship is not unique, of the approximately 8,800 species of ants, at least 200 have evolved some form of symbolic relationship with one another (Topoff 1999). What makes Polyergus special is how a newly mated queen can, all by herself, takeover a Formica nest and start a new colony. This article looks at not only this unique behavior, but at the biological mechanisms that facilitate its occurrence; how these and the social parasite system might have evolved in Polyergus breviceps.

The Polyergus slave raids and colony takeovers

Polyergus males (raiders) will emerge from their nest (a mixed nest where Formica workers are already enslaved) and forage for a suitable raid target. If one is found, the male will return to the nest, rally the other Polyergus, and head out in a raiding column. If it was another Polyergus colony, a nasty and high cost territorial battle ensues. If it was a Formica nest, the Polyergus incite a “panic-flee” response from the Formica by releasing formic acid and take the Formica pupae back to their nest to be a slaves. Occasionally, a new queen will embark on a raiding column with the other Polyergus. She will then, after mating, leave the column and forage for a suitable Formica nest (Topoff 1999). Howard Topoff did a considerable amount of work in evaluating how the queen then takes over the colony. After finding a Formica nest, the queen finds an entrance and is immediately attacked by Formica worker. The queen responds by biting with her sharp mandibles and releasing a pheromone from her enlarged Dufour’s gland that, unlike many other parasitic ants, has a pacifying effect. The queen quickly searches for and locates the Formica queen and, with her adapted mandibles, proceeds to bite and lick various parts the Formica queen for an average of 25 minutes (Topoff 1993). “Within seconds of the host queens death, the nest undergoes a most remarkable transformation” (Topoff 1999). The Formica workers cease aggression and start to groom the Polyergus queen as if it were their own (Topoff 1999). The takeover now complete, the Polyergus queen gains not only a nest, but a worker caste as well. She then lays her eggs and the cycle continues.


=The Polyergus slave raid and colony takeover mechanisms=

It is worth mentioning briefly that nearly all slave making ants have mandibular adaptations that help them attack others; Polyergus is no different.

Specific to Polyergus, when the queen first enters a Formica nest she releases a pheromone from her enlarged Dufour’s gland. Topoff did experiments to show that this pheromone has an important facilitative effect in colony usurpation; it reduces the aggression of the attacking Formica workers. They took the Dufour’s, pygidial, and poison glands from freshly mated Polyergus queens, using water as a negative control. These were crushed in distilled water to make a solution containing their extracts. Because it was impossible to prevent a Polyergus queen from secreting their own pheromones during a live encounter, they used the harvester ant Pogonomyrmex occidentalis (naturally attacked by Formica) as the subject. These ants were dipped in the above solutions, one ant/solution/test at a time, and placed in a petri dish with three Formica Occulta “attackers”. They were observed for three minutes to see how long the Pogonomyrmex was attacked (Topoff 1988). The results were as follows: “the mean duration of aggression by the Dufour’s gland treatment was 53.3 seconds...The mean duration of aggression for the water, pygidial gland, and poison gland controls were: 143.5 seconds, and 137.2 seconds and 132.2 seconds respectively” (Topoff 1988). Apparently, at some time, Polyergus queens evolved the capacity to passively facilitate colony takeovers.

Topoff and Ellen Zimmerli also did experiments to prove that the Polyergus queen “tricks” the Formica colony by obtaining chemicals from the Formica queen in the process of killing her. In one test, the Formica queen was killed (by flash freezing then thawing) prior to Polyergus contact. Even though it was already dead, the Polyergus sit bit, stabbed, and licked the queen just as if it were alive: and the Polyergus was consequently accepted by the colony (Topoff 1993). Another test showed that if no Formica queen was present, then Polyergus had little chance of a successful takeover. Clearly, the Formica queen is providing some sort of chemical(s) to the Polyergus queen, however unintentionally. That take over can occur even if the host queen is dead, but not if she is not present, proves that chemical absorption is important. The Polyergus queen need only kill one host queen to be adopted. If the colony was polygynistic, the Polyergus queen can take her time finding the other queens. “Hour by hour, day by day, she methodically locates and kills every Formica queen, sometimes taking several weeks to clear out all remnants of opposition” (Topoff 1999).

The evolution of Polyergus

Considerable work has been published on the evolution of ant dulosis and almost all of it has at least some empirical evidence to defend its positions. Notably, that nearly all raiding ant species have is an adaptation of their mandibles that make them big or piercing or both. It makes sense that the very thing that enables an ant to be a better raider causes that same ant to become dependent on others; the parasite loses the use of its mandibles for actual work. On this and other evidence, it has been proposed that a predation is the precursor to slavery (Buschinger 1988). It has also been suggested that colony multiplication by adoption and budding followed by temporary parasitism can lead to dulosis. While observations indicate that colony multiplication can lead to temporary parasitism, it is apparently very questionable that temporary parasitism leads to dulosis (Buschinger 1988). In addition, about 90 years ago, Carlo Emery observed that “the slave-making temporarily and permanently parasitic ants originate from closely related forms which serve them as host” (*Emery 1909). Jurgen Heinze did a series of experiments that prove this observation, known today as Emery's Rule. Rather than just relying solely on morphological cues, he used enzyme gel electrophoresis assays to create a detailed phylogenetic picture of host and parasite connections (Heinze 1991). His experimental results support a loose version of Emery’s rule. On one end of the spectrum, they saw near identical electromorphs between species in most host and parasite pairs studied. However, it also appears that at least one example does not support Emery’s rule (Leptothorax paraxenus), which differed from its host in several electromorphs (Heinze 1991). The selective forces involved in the evolution of social parasitism are not fully understood, and it is unlikely that one model will fit all relationships. “Any hypothesis explaining the evolution of slavery in Polyergus must account both for the origin of group raiding with brood capture, and for non-independent colony foundation by queens” (Topoff 1990). Topoff gives an adequate hypothesis to the evolution of Polyergus by integrating three processes: queen takeover, olfactory imprinting, and territorial fighting (Topoff 1990). Here are his main points. A free-living ancestor of Polyergus, that is a scavenger, would band together with others for intraspecific contest. Occasionally a queen would invade colonies of Formica. Initially the queen would drive off the Formica queen and workers and appropriated the Formica pupae (he gives as example the queens of Formica Wheeleri that do this now). The killing of the Formica queen and adoption by the workers would evolve from this. His previous work (which was presented earlier) shows what would have evolve for adaptation to occur: “(1) sharp mandibles for killing the Formica queen, (2) a pheromone that reduces aggression from resident workers, (3) a tendency to hold onto the dead Formica queen long enough to absorb her odors...” (Topoff 1999). The next step would be olfactory imprinting between the two species, a consequence of living one’s life from start to finish in the presence of both species. Polyergus’ ancestor then forages and encounters a colony of the same species. Again, they recruit nestmates to a territorial raid. In a brilliant insight, Topoff suggest this trait explains the raiding behavior. The Polyergus worker, raised by Formica as conspecifics, “identifies individual of Formica as belonging to its own species, another territorial raid is incited. Thus from the standpoint of Polyergus... slave raids are equivalent to territorial raids” (Topoff 1990). The captured brood is imprinted as well and they become workers in the original nest. As time went on “Our ancestral Polyergus could easily slide in the direction of facultative parasitism” (Topoff 1990). Eventually, Polyergus ancestors lost the ability to take care of themselves and become the inquiline Polyergus we see today.

References

Buschinger, A. (1986). Evolution of social parasitism in ants. Trends Ecol. Evol. 1:155-160

• Emery, C. (1909). Biol. Centralblatt. 29, 352

Heinze, J. (1991). Biochemical studies on the relationship between socially parasitic ants and their hosts. Biochem. Syst. Ecol. 19: 195-206-Shald Ague.

Topoff H., Cover, S., Greenburg. L., Goodloe, L., and Sherman, P. (1988). Colony founding by queens of the obligatory slave-making ant Polyergus breviceps: The role of the Dufour’s gland. Ethology 78:209-218.

Topoff, H. (1990). The evolution of slave-making behavior in the parasitic ant genus Polyergus. Ethol. Ecol.. Ecol. 2: 284-287.

Topoff H. and Zimmerli, E. (1993). Colony takeover by a socially parasitic ant, Polyergus breviceps: the role of chemicals obtained during host queen killing. Anim Behav. 46, 479-486.

Topoff, H. (1999, Nov.). Slave-Making Queens. Scientific American. 281, 5:84-90.

ource

† Social Insects Specialist Group 1996. [http://www.iucnredlist.org/search/details.php/17927/all "Polyergus breviceps"] . [http://www.iucnredlist.org 2006 IUCN Red List of Threatened Species. ] Downloaded on 10 August 2007.


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