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Identification

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Identification in the Nearctic Southwest: the frontal carinae extend about  the length to the occiput, and the occipital lobes are covered with coarse rugae. The mesosoma has numerous spines and the gaster is covered with tubercles. Ants of this genus have 11 segmented antennae in which the insertion is hidden by the frontal lobes. Most tubercles and spines have a curved, coarse hair. In North America, it could only be confused with Trachymyrmex, from which it differs in being polymorphic. Atta also occurs in the United States (southern AZ, southern TX), and is similar to Acromyrmex, but differs in that the dorsum of the gaster is smooth (no tubercles).(From Mackay and Mackay, 2002).
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AntWeb. Version 8.45.1. California Academy of Science, online at https://www.antweb.org. Accessed 15 December 2022.
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Taxonomic History

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Atta (Moellerius) versicolor Pergande, 1893 PDF: 31 (w.) MEXICO. Nearctic. Primary type information: Calamajué (as Calamujuet) [29°38′N 114°25′W], Baja California, Mexico; CASTYPE00618; BMNH AntCat AntWiki HOL

Taxonomic history

Wheeler, 1907d PDF: 704 (q.m.).Combination in Atta (Acromyrmex): Emery, 1895d PDF: 330.Combination in Atta (Moellerius): Emery, 1905f: 108.Combination in Acromyrmex (Moellerius): Emery, 1924f PDF: 351.Senior synonym of Acromyrmex versicolor chisosensis: Shattuck & Cover, 2016 10.11646/zootaxa.4175.1.2 PDF: 11.See also: Fowler, 1988b: 291.
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AntWeb. Version 8.45.1. California Academy of Science, online at https://www.antweb.org. Accessed 15 December 2022.
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Distribution

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Acromyrmex versicolor nests are common in the Sonoran Desert (southwestern North America) and are also known to occur in western Texas.
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Life Cycle

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Mating flights take place in late summer or early fall on a day following substantial rains. Large mating aggregations can occur with swarms of alates forming elliptical columns above a high bush or other prominent structure (Johnson and Rissing 1993). Wheeler’s (1917) striking account of one such mating swarm provides interesting details about this phenomenon:

“We had left our camp July 30 about 30 miles north of Florence, Ariz., and were crossing the desert on our way to Phoenix. The air was very still and clear after a heavy rain on the preceding day. At 5.50 a. m., just after sunrise, we entered a region several miles in extent where the marriage flight of Acromyrmex (Atta) versicolor was in full swing. The ants were aggregated in numerous sharply defined swarms, each of which was egg-shaped or elliptical, about six to ten feet long and three to four feet broad, stationary some twenty to thirty feet above and with its long axis perpendicular to the surface of the earth. In some places the swarms were only about forty or fifty feet apart but more frequently the distance between them was fully a hundred feet or as many yards. As far as the eye could see over the desert similar swarms could be discerned. Within each swarm the large dark brown males and females were darting about in vertiginous, zigzag flight: Closer examination showed that each swarm was constantly receiving single males and females flying straight to it from a distance, but it did not grow in size because pairs of ants in copula were constantly raining down to the ground from its lower extremity, so that under each swarm there was a dense layer, often a yard or more in diameter, of writhing and struggling ants. One of the swarms happened to be poised above a puddle of water so that the surface of the latter became black with the fallen pairs. We rode for fully half an hour through these swarms, which must have comprised hundreds of thousands of ants. The activity of the insects was truly surprising, for the workers of versicolor are sedate and slow-moving like all other Attii. The whole phenomenon was rendered remarkably clear and striking by the large size and dark color of the ants and their wings, the stillness and purity of the air and the unobstructed view over the level desert.”

Queens will forage outside of their newly founded nests to collect plant material for their nascent fungus gardens. Workers forage along trails, which extend up to 17m, and also forage singly. Acromyrmex versicolor collect both dry and green vegetation. Dry grasses made up a major portion of foraged items in one study population, located 30 miles N.E. of Tempe Arizona (Gamboa 1975). It was also found that a bias for collecting dried vegetation would shift to a preference for green vegetation after periods of heavy rain. Foragers will climb on the desert plants and remove live leaves by excising the petioles.

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Brief Summary

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A desert species that is common in the Sonoran Desert of southwestern North America. These ants collect live and dead vegetation to use for the fungus gardens that they cultivate within their nests. This fungus is their primary food source. New colonies of this species can be founded haplometrotically or pleometrotically. Numerous studies have investigated fitness consequences and behavioral aspects of pleometrosis in Acromyrmex versicolor (e.g. Rissing et al. 2000, Cahan and Julian 1999, Hagen et al. 1988). Queens are polyandrous, which is an unusual trait in ants.
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Foraging

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Foraging activity is temperature dependent (Gamboa 1976) with workers active above ground at surface temperatures between 7.7 and 44 C. During the summer the ants are primarily nocturnal. Beyond the hottest months of the year there is a shift to a diurnal activity pattern, with morning and afternoon foraging bouts beginning and ending with daily changes in temperature.
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Male

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(W.M. Wheeler 1907). Length: 8 mm. Head, without the mandibles and eyes, as long as broad, subrectangular, with nearly straight posterior border. Eyes large, protruding, hemispherical, with their posterior orbits at the middle of the head. Mandibles well-developed, acute, flattened and multidentate. Clypeus very faintly and sinuately excised in the middle. Frontal and lateral carinae without teeth. Antennal scapes extending ,fully 1/3 their length beyond the posterior corners of the head. The latter with a small, acute superior and a broad flattened inferior tooth on each side. Pronotum with a larger inferior and much smaller superior tooth on each side. Mesonotum with distinct Mayrian furrows. Scutellum with a median longitudinal depression and a pair of blunt posterior teeth. Epinoturn with short, convex base and longer straight declivity; spines like those of the female but more slender and tapering more gradually. Petiole and postpetiole like those of the female, the former with small acute teeth above and three lateral teeth, the latter with four teeth on each side. Gaster broadly elliptical, with the basal segment flattened above and without tubercles. Genital appendages convex, curved inward, with broad, rounded, subtruncate tips. Legs slender. Body including the mandibles and legs, opaque; gaster slightly shining. Mandibles finely striated and coarsely punctate. Head, thorax and pedicel densely rugulose, the rugulae being longitudinal on the head, mesonotum, scutellum, pleurae and epinotum, and transverse on the pronotum, petiole and postpetiole. Gaster and legs densely punctate. Genital appendages with a few scattered foveolm.

Pilosity like that of the worker and female.

Black; mandibles, border of clypeus, frontal carinae; neck, antennae, coxae, tibiae, tarsi and gaster ferruginous brown, posterior borders of gastric segments and genitalia somewhat paler. Wings like those of the female.

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Queen

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(W.M. Wheeler 1907). Length: 8mm. Head resembling that of the worker, but the posterior corners are more acute and the antennal scapes are longer. Pronotum with two broad and rather blunt inferior and two acute superior spines, which are directed forward and outward. Scutellum trapezoidal with bidentate posterior edge. Epinotal spines long, curved and diverging, of nearly uniform thickness up to their rapidly tapering tips which are bent downwards. Petiole and postpetiole similar to those of the worker, but the median pair of teeth in the former longer than the lateral pair and the spines on the postpetiole reduced to small teeth. Gaster pyriform, with the first segment flattened above and without the pointed tubercles.

Mandibles and legs shining; remainder of body opaque. Head coarsely, densely and crenately rugose, the rugae being longitudinal on the sides but diverging from the front and median line on the upper surface. Thorax covered with rugae similar to those on the head, transverse on the pronotum, longitudinal on the mesonotum and pleurae, and irregular on the scutellum. Pedicel and gaster densely and irregularly rugulose; on the middle of the first segment of the latter the rugulae are more regular and longitudinal. Antennal scapes and legs 'coarsely punctate 'and more or less roughened.

Pilosity like that of the worker.

Ferruginous brown; upper surface of head, mesonotum and gaster blackish, the mesonotum with a V-shaped red spot on the middle and the gaster with a pair of elliptical ferruginous spots on the basal segment. Wings opaque yellowish brown, with dull yellow veins.

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Worker

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(Pergande 1893). Length, about 6 mm. Color reddish-brown. Eyes and apical edge of mandibles, black. All depressions and all prominences appear to be black in a certain light, while the nodes and the abdomen, if viewed from above or in certain directions from the side, have a bright coppery reflection.

Head wider than long, deep and angularly emarginate behind; a rather broad, shallow frontal channel and laterally carinated area beyond insertion of antennae. Posterior angles of head rounded and with a row of six or more short denticles, the last one somewhat longest; three or more teeth may also be observed along the posterior ventral edge each side, the anterior one of which being longest. Frontal laminae broad, somewhat longer than wide, bifid at upper angle; interno-ocular carinae distinct, curved inwards. Clypeus broadly triangular, slightly arcuate in front, with a slight median emargination. Mandibles large, triangular, their apical edge almost straight and furnished with four to six blunt, rudimentary teeth. Scape of antennae rather short, reaching but little beyond posterior angles of the head. Thorax of the usual shape in this genus. Prothorax with two stout spines each side, the anterior pair farthest apart, longest, inclining forward, the other two stouter, directed backward and outward; two short, stout, backward directed median tubercles or spines in front of the middle of the mesothorax and a still shorter one each side of them at the anterior margin. Metathorax with a deep median depression, the upper edges quite acute, terminating anteriorly in a small tooth like projection. Metathoracic spines rather long and slender, curved backward and outward.

First node of petiole triangular from a lateral view, its two dorsal and the lateral faces quite flat, the edges acute; the upper edges are provided anteriorly with two short, stout teeth, and laterally with two to three smaller denticles each side; there is also a forward directed, acute ventral tooth at base. Second node wider than long, rounded in front and at sides, truncate behind, concave above, the edges acute and beset with four or five short, acute teeth; there is also a prominent lateral Carina, furnished with four or five teeth, and two ventral teeth.

Abdomen of the normal shape, the first segment with a depressed median line, and each lateral half with about twenty-five teeth, some of them bifid, arranged in irregular rows. The other segments without teeth or tubercles.

Head, pro and mesothorax rugoso-granulate; the metathorax, legs, nodes and abdomen densely and finely granulate. Erect pubescence stiff and blackish, the appressed pubescence yellowish.

This appears to be related to A. coronata Fab. which differs from this species in the comparatively smoother surface of every part of the body, the longer mandibles and antennae, more numerous and longer denticles of the head, much longer spines of the thorax, lower anterior node and larger and more flattened posterior node of the petiole.

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Acromyrmex versicolor

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Acromyrmex versicolor is known as the desert leafcutter ant. A. versicolor is found during the summer months in the Colorado and Sonoran deserts when there is precipitation. They form large, distinctive nest craters that are covered with leaf fragments. Living and dead leaves are collected by workers and used to cultivate fungus gardens.[2] Each colony can have multiple queens, if they do this is a practice called polygyny, and each queen has her own batch of “starter” fungus. This species does not sting.

Identification

The average worker is 2–6 mm long. Individuals of A. versicolor are a variety of sizes due to the division of labour seen within their colony.[3] They are reddish brown and have a narrow waist. They are also covered in spines; at least 4 spines on the rear of their thorax, distinct spines on the rear corners of their head, and small bumps on their abdomen.

Mating

A. versicolor mate from late July through October.[4] All major mating flights are preceded by a day of rain. Mating flights begin in the early morning when individuals of both sexes emerge from the colony. Males will leave for the mating sites first, followed by the females who likely follow male pheromones. Males will grapple the female in mid-air then fall to the ground to copulate.

Polyandrous mating has the potential to reduce genetic relatedness of individuals within a colony, which may have a profound effect on the colony's stability and social structure. Up to nine males have been reported surrounding a single female. Females have also been known to mate with multiple males. Females will often mate with up to three or four different males even though one mating is sufficient to fill the spermatheca.[5] Genetic analysis of paternity of offspring of females who mated with multiple males showed that each male had relatively equal amounts of offspring. This shows that the sperm is mixed within the spermatheca and that females have little to no control over which sperm fertilize her eggs.

Effects of Temperature

The foraging habits of A . versicolor are strongly influenced by temperature.[6] During the cooler spring and fall months, A. versicolor have diurnal foraging activity. During the hotter summer months, they tend to forage more at night when the soil temperatures are cooler. When temperatures are their hottest and individuals find themselves stranded away from the nest, they will find a cooler surface such as a rock and press their body against it to try and lose heat. The ideal foraging temperatures of A. versicolor vary from 12 °C to 42 °C.[7]

Temperature also plays a role in how deep a queen will make her nest. Nests have to be made at a depth below where lethal temperatures occur (below 5 cm).[8] Building nests under trees allows colonies to remain below lethal temperatures and also does not require them to be so deep (2–3 cm). Having a nest under a tree also allows colonies to be closer to food sources such as leaves.

Foraging

A. versicolor use trails to forage in groups like most higher attines, but also forage alone which is a characteristic of more primitive leafcutter ants.[9] They forage for both green vegetation and dry grasses, but dry grasses make up the bulk of their forage. A. versicolor will increase the amount of fresh vegetation they collect after significant amounts of rainfall, but will collect dry grasses during drier periods.

The amount an individual ant forages or the efficiency to which each ant forages may be due to each ones genetics and may vary significantly between matrilines.[10] Younger ants most often spend their time tending to the nest while older ants will go out and forage. The age at which a young ant will switch to foraging also seems to be genetically predisposed.

See also

References

  1. ^ "Species: Acromyrmex versicolor". AntWeb. 2010-06-30. Retrieved 2010-08-20.
  2. ^ [Evans, A. (2008). Field Guide to Insects and Spiders of North America. New York: Sterling Publishing.]
  3. ^ Camargo, R.S., et al. (2007). Age polyethism in the leaf-cutting ant Acromyrmex subterraneus brunneus Forel, 1911 (Hym., Formicidae). Journal of Applied Entomology 131: 139-145.
  4. ^ Johnson R. A. and S.W. Rissing. (1993). Breeding Biology of the Desert Leaf-Cutter Ant Acromyrmex versicolor (Pergande) (Hymenoptera: Formicidae). Journal of the Kansas Entomological Society 66: 127-128
  5. ^ Reichardt, A. K. and D.E. Wheeler. (1996). Multiple Mating in the Ant Acromyrmex versicolor: A Case of Female Control. Behavioral Ecology and Sociobiology 38: 219-225.
  6. ^ Gamboa, G. J. (1976). Effects of Temperature on the Surface Activity of the Desert Leaf-cutter Ant, Acromyrmex versicolor versicolor (Pergande) (Hymenoptera: Formicidae). American Midland Naturalist 95: 485-491.
  7. ^ Murray, S. L. (1972). Foraging of the leaf-cutter ant Acromyrmex versicolor Perg. in relation to season, temperature, relative humidity, and rainfall. M.S. Thesis. Univ. Arizona, Tucson. 1-23.
  8. ^ Rissing, S.W., R.A. Johnson, and G.B. Pollock. (1986). Natal Nest Distribution and Pleometrosis in the Desert Leaf-Cutter Ant Acromyrmex versicolor (Pergande) (Hymenoptera: Formicidae). Psyche a Journal of Entomology 93: 177-186.
  9. ^ Gamboa, G. J. (1975). Foraging and Leaf-Cutting of the Desert Gardening Ant Acromyrmex versicolor versicolor (Pergande) (Hymenoptera: Formicidae). Oecologia 20: 103-110.
  10. ^ Julian, G. E. and J. H. Fewell. (2004). Genetic variation and task specialization in the desert leaf-cutter ant, Acromyrmex versicolor. Animal Behaviour 68: 1-8.

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Acromyrmex versicolor: Brief Summary

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Acromyrmex versicolor is known as the desert leafcutter ant. A. versicolor is found during the summer months in the Colorado and Sonoran deserts when there is precipitation. They form large, distinctive nest craters that are covered with leaf fragments. Living and dead leaves are collected by workers and used to cultivate fungus gardens. Each colony can have multiple queens, if they do this is a practice called polygyny, and each queen has her own batch of “starter” fungus. This species does not sting.

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