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Home -> Kingdom Animalia -> Phylum Arthropoda -> Class Insecta -> Order Lepidoptera -> Suborder Macrolepidoptera -> Family Lycaenidae -> Species Atlides halesus

Atlides halesus



2008/10/05 10:31:43.094 GMT-4

By Camilia VanCamp

Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Suborder: Macrolepidoptera
Family: Lycaenidae
Genus: Atlides
Species: Atlides halesus

Geographic Range

Atlides halesus, butterflies commonly known as great purple hairstreaks, are found from Guatemala north to the southern United States. Although they have been seen as far north as Maryland and Oregon, in the interior states they generally stay below the 38th parallel. (Scott, 1986; Struttman, 2001; Tveten and Tveten, 1996)

Biogeographic Regions:
nearctic (native ); neotropical (native ).

Habitat

Atlides halesus live in wooded areas, especially those that are infested with mistletoe, Phoradendron spp. (Scott, 1986; Struttman, 2001)

These animals are found in the following types of habitat:
temperate .

Terrestrial Biomes:
forest .

Physical Description

Wingspan
30 to 50 mm; avg. 40 mm
(1.18 to 1.97 in; avg. 1.57 in)


Atlides halesus are relatively large butterflies, with a wingspan ranging from 30mm to 50mm. The upper side of their wings is black with brilliant iridescent blue. Below, the wings are a purplish black color with gold iridescent markings near the tails. Atlides halesus have two tails attached to each hind wing, one shorter than the other. The underside also has red spots near the attachment to the abdomen. The abdomen is blue on top and red-orange underneath. Females are slightly larger and duller than males.

Atlides halesus larvae are green with dark green bands, yellow stripes, and a narrow green mid-dorsal line. They are also covered in short orange and green hairs.

The pupae are mottled brown and black. (Hall and Butler, 1999; Milne and Milne, 1992; Scott, 1986; Struttman, 2001; Tveten and Tveten, 1996)

Some key physical features:
ectothermic ; heterothermic ; bilateral symmetry .

Sexual dimorphism: female larger, male more colorful.

Development

Female Atlides halesus scatter their eggs over mistletoe, Phoradendron spp. The larvae hatch and eat the mistletoe until they are fully grown. Then they journey to crevices under the bark or at the base of the host tree where they can safely pupate throughout the winter; in the spring, butterflies emerge. (Hall and Butler, 1999; Tveten and Tveten, 1996)

Special features of growth:
metamorphosis .

Reproduction

Breeding season
March-November

Male Atlides halesus will wait on treetops or hilltops from noon to untill sundown (earlier on colder days) for a female to fly by. This mating system is called landmark based. Males will move their wings up and down to attract females. After mating, females will scatter their eggs over mistletoe, Phoradendron spp., so that the larvae will be able to eat. They breed from March through November, each female laying several broods each. (Preston-Mafham and Preston-Mafham, 1993; Scott, 1986; Tveten and Tveten, 1996)

Male Atlides halesus often return to the same treetop or hilltop for days at a time to await new mates. (Scott, 1986)

Key reproductive features:
seasonal breeding ; sexual ; fertilization (internal ); oviparous .

After female Atlides halesus lay their eggs it is up to the larvae to feed and protect themselves. (Tveten and Tveten, 1996)

Parental investment:
no parental involvement; pre-fertilization (provisioning, protecting: female).

Lifespan/Longevity

Average lifespan (wild)
24 days

After emerging from the pupae, Atlides halesus live for about 24 days. (Scott, 1986)

Behavior

Male Atlides halesus remain local, returning often to the same treetop or hilltop to await a mate. The flowers adults frquent for nectar do not grow at this elevation, so treetops and hilltops serve only as a place to find mates. This is called hilltopping. While hilltopping, they move their wings up and down to attract mates and can trick predators into going after their false head on their wings. When they fly, they do so very slowly. Larvae also move fairly slowly and are slug-like. The adults make several flights through March and November, and fly all year in Florida and South Texas. The pupae hibernate through the winter. (Hall and Butler, 1999; Milne and Milne, 1992; Preston-Mafham and Preston-Mafham, 1993; Scott, 1986)

Key behaviors:
flies; diurnal ; motile ; migratory ; hibernation ; social .

Communication and Perception

Atlides halesus communicate with potential mates by flapping their wings up and down while on treetops or hilltops. (Hall and Butler, 1999; Preston-Mafham and Preston-Mafham, 1993)

Communicates with:
visual .

Perception channels:
visual .

Food Habits

The larvae of Atlides halesus eat only mistletoe. The younger caterpillars eat the epidermis of the leaf while the older larvae eat the entire leaf. Adults drink the nectar of various flowers in the family Asteraceae, including goldenrods and ragworts. (Scott, 1986; Tveten and Tveten, 1996)

Primary Diet:
herbivore (folivore , nectarivore ).

Plant Foods:
leaves; nectar.

Predation

Known predators

Adult Atlides halesus protect themselves from predators by moving their wings up and down to draw attention to their false heads made by the tails and spots on the hind wings. Thus, if a predator attacks a butterfly by grabbing its tail, the tail will break off and the butterfly can escape.

Camouflage protects both larvae and pupae from large prey, but Atlides halesus have not developed a mechanism to protect the pupae from parasitoid wasps and tachinid flies. (Hall and Butler, 1999; Tveten and Tveten, 1996)

Ecosystem Roles

Adult Atlides halesus help to pollinate various flowers in the family Asteraceae. Larvae help control mistletoe populations by eating the mistletoe leaves. The pupae provide a home and food for the developing parasitoid wasps and tachinid flies. (Hall and Butler, 1999; Scott, 1986; Tveten and Tveten, 1996)

Key ways these animals impact their ecosystem:
pollinates; creates habitat.

Economic Importance for Humans: Negative

None known

Economic Importance for Humans: Positive

None known

Conservation Status

IUCN Red List: [link]:
Not Evaluated.

US Migratory Bird Act: [link]:
No special status.

US Federal List: [link]:
No special status.

CITES: [link]:
No special status.

The Nature Conservancy Global Rank gives Atlides halesus a ranking of G5, which means that the species is secure globally, although it may be rare in the periphery of its habitat range. (Struttman, 2001)

Other Comments

Atlides halesus are the only species within the genus Atlides. (Arnett, 1985; Holland, 1910)

Contributors

Sara Diamond (editor), Animal Diversity Web Staff.

Camilia VanCamp (author), Southwestern University.
Stephanie Fabritius (editor), Southwestern University.

References

Arnett, R. 1985. American Insects. New York: Van Nostrand Reinhold Company.

Hall, D., J. Butler. 1999. "University of Florida Department of Entomology and Nematology" (On-line). Accessed November 28, 2001 at http://creatures.ifas.ufl.edu/bfly/purple_hairstreak.htm.

Holland, W. 1910. The Butterfly Book. Golden City, New York: Doubleday, Page, & Company.

Milne, L., M. Milne. 1992. The Audubon Society Field Guide to North American Insects and Spiders. New York: Alfred A. Knopf, Inc..

Preston-Mafham, R., K. Preston-Mafham. 1993. The Encyclopedia of Land Invertebrate Behavior. Cambridge, Massachusetts: The MIT Press.

Scott, J. 1986. The Butterflies of North America. Stanford, California: Stanford University Press.

Struttman, J. 2001. "National Prairie Wildlife Research Center" (On-line). Accessed November 28, 2001 at http://www.npwrc.usgs.gov/resource/distr/lepid/bflyusa/nj/282.htm.

Tveten, J., G. Tveten. 1996. Butterflies of Houston & Southeast Texas. Austin, Texas: University of Texas Press.

2008/10/05 10:31:44.349 GMT-4

To cite this page: VanCamp, C. 2001. "Atlides halesus" (On-line), Animal Diversity Web. Accessed October 11, 2008 at http://animaldiversity.ummz.umich.edu/site/accounts/information/Atlides_halesus.html.

Disclaimer: The Animal Diversity Web is an educational resource written largely by and for college students. ADW doesn't cover all species in the world, nor does it include all the latest scientific information about organisms we describe. Though we edit our accounts for accuracy, we cannot guarantee all information in those accounts. While ADW staff and contributors provide references to books and websites that we believe are reputable, we cannot necessarily endorse the contents of references beyond our control.

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