common name: zebra swallowtail, pawpaw butterfly, kite swallowtail, ajax
scientific name: Eurytides marcellus (Cramer) (Insecta: Lepidoptera: Papilionidae)
The zebra swallowtail is our only native kite swallowtail (tribe Leptocircini [=Graphiini]). Two other species rarely stray into Texas and Florida. The zebra swallowtail is one of our most beautiful swallowtails. Unlike most of our other native swallowtails, they are not involved in a mimicry complex.
The zebra swallowtail is widely distributed from southern New England west to southern Minnesota and south to eastern Texas and Florida.
The wingspread of males is 3.0 to 4.6 cm and females 2.9 to 4.9. cm. The upper surface of the wings is white with black stripes. The hind wings have very long tails. The zebra swallowtail exhibits seasonal dimorphism. Early spring specimens are lighter in color, smaller, and have tails only about half as long as summer forms.
adult summer form
Eggs are pale green. Young larvae are dark colored with many transverse black, yellow, and white bands. Older larvae are green with broad blue, black, and yellow transverse bands between the thorax and abdomen and usually yellow bands between abdominal segments and numerous fine transverse black lines on thorax and abdomen. However, larvae exhibit color polymorphism. The osmeterium is yellow. Pupae are green or brown with light lines simulating a leaf-like texture and are supported with a silken girdle.
young larva
full-grown larva
pupa
There are two flights in the North and many flights in Florida from March to December. The host plants are Asimina species (pawpaws) (Annonaceae). Throughout most of the range of the zebra swallowtail, Asimina triloba (L.) Dunal is the only host. In the Southeast, a variety of other Asimina species are utilized. A commonly-used host in central Florida is A. angustifolia Raf.
slimleaf pawpaw
Males patrol for females in the vicinity of host plants, and females frequently may be observed ovipositing on host foliage. Adults seek nectar at a variety of flowers and also obtain moisture from mud.
Females select plants with young leaves for oviposition. Eggs are laid singly on the young leaves, and larvae feed on foliage (and flowers when available). This requirement for new leaves may limit reproduction of E. marcellus in summer and fall. Production of new leaves is often stimulated during this period by defoliation of the host plant by the pyralid moth, Omphalocera munroei Martin. Therefore, abundance of late flights of E. marcellus may be dependent on abundance of this moth.
Larvae have an extrusible osmeterium that is coated with strongly smelling chemicals (isobutyric and 2-methyl butyric acids). When disturbed, they extrude the osmeterium and smear the offender with the chemicals. This has been shown to be an effective defense against small ants and spiders, but not against most other predators. Osmeterial defense is also ineffective against the ichneumonid parasitoid of papilionids, Trogus pennator (Fabricius), which does not trigger extrusion of the osmeterium with its attacks. Other defensive measures utilized by the larvae are to drop off the host plant when disturbed by a potential predator and for third, fourth, and fifth instar larvae to rest off the plant in leaf litter when not feeding.
Pupation usually occurs on the under sides of leaves of the host plant. Some pupae of each flight overwinter. Short photoperiod produces diapausing pupae that hibernate.
- Damman H. 1989. Facilitative interactions between two lepidopteran herbivores of Asimina. Oecologia 78: 214-219.
- Damman H. 1986. The osmeterial glands of the swallowtail butterfly Eurytides marcellus as a defense against natural enemies. Ecological Entomology 11: 261-265.
- Damman H, Feeny P. 1988. Mechanisms and consequences of selective oviposition by the zebra swallowtail butterfly. Animal Behaviour 36: 563-573.
- Daniels JC. 2000. Butterflies 2: Butterflies of the Southeast. UF/IFAS. Card Set. SP 274.
- Eisner T, Pliske TE, Ikeda M, Owen DF, Vásquez L, Pérez HP, Franclemont JG, Meinwold J. 1970. Defense mechanisms of arthropods. XXVII. Osmeterial secretions of papilionid caterpillars (Baronia, Papilio, Eurytides). Annals of the Entomological Society of America 63: 914-915.
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- Mather B. 1970. Variation of Graphium marcellus in Mississippi (Papilionidae). Journal of the Lepidopterists' Society 24: 176-189.
- Medley JC, Fasulo TR. (1998). Florida Butterfly Tutorials. University of Florida/IFAS. CD-ROM. SW 155.
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- Oppler PA, Krizek GO. 1984. Butterflies East of the Great Plains. The Johns Hopkins University Press. Baltimore, MD.
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- Scriber JM, Tsubaki Y, Lederhouse RC, Eds. 1995. Swallowtail Butterflies: Their Ecology and Evolutionary Biology. Scientific Publishers, Inc. Gainesville, FL.
- Tyler H, Brown KS Jr, Wilson K. 1994. Swallowtail Butterflies of the Americas. Scientific Publishers, Inc. Gainesville, FL.
- West DA, Hazel WN. 1996. Natural pupation sites of three North American swallowtail butterflies: Eurytides marcellus (Cramer), Papilio cresphontes Cramer, and P. troilus L. (Papilionidae). Journal of the Lepidopterists' Society 50: 297-302.
Authors: Donald W. Hall and Jerry F. Butler, University of Florida
Photographs by: Jerry F. Butler and Donald W. Hall, University of Florida
Project Coordinator: Thomas R. Fasulo,University of Florida
Publication Number: EENY-58
Publication Date: September 1998. Latest revision: July 2007.
Copyright 1998-2007 University of Florida
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