common name: larger canna leafroller
scientific name: Calpodes ethlius (Stoll) (Insecta: Lepidoptera: Hesperiidae)
Flowering canna plants (several species of Canna) make beautiful additions to the landscape in
Florida home gardens and on public or commercial property. Cannas (see University of Florida
Fact Sheet " Cannas for the Florida Landscape")
are easy to grow, have few disease problems, and produce lush tropical-looking foliage and
showy colorful flowers. However, cannas can be decimated by leaf-chewing insects, such as
grasshoppers and leaf-rolling caterpillars. Two caterpillars, in particular, are very destructive to
canna in Florida, the larger canna leafroller, Calpodes ethlius (Stoll), whose adult form is
variously called the Brazilian skipper, the canna butterfly, or the arrowroot butterfly (Moore
1928), and the lesser canna leafroller, Geshna cannalis
(Quaintance) .
Calpodes ethlius is native to Mexico, Central America, and the northern part of the South
American continent, being found as far south as the northern border of Argentina (Scudder
1889). It is found on the Galapagos Islands in the Pacific Ocean (Onore and Mielke 1988) and
throughout the West Indies in the Caribbean Sea. In the United States, it is well-established in
Florida, Texas, and southern Arizona (Scudder 1889). It is an occasional visitor to other Gulf
coastal states and can be found in coastal Georgia and South Carolina. To date, C. ethlius has
been collected in at least 24 states (see Butterflies of North America), although many of those records are considered to be "strays" rather than indications of establishment.
The adults of C. ethlius are brownish skipper butterflies of medium size. The female's forewing
ranges from 22 to 27 mm in length while that of the male is somewhat smaller at 23 to 24 mm
(Scudder 1889). The forewings are rich dark brown except for five vitreous (transparent) spots
and have a fringe of dirty golden yellow hairs on the posterior margin. The hind wings are a
little darker than the forewings and have three vitreous spots arranged in an almost straight line.
The dorsal surface of the thorax is olive-colored while the ventral surface is yellowish gray. The
abdomen is dark brown dorsally and pale yellow whitish ventrally. Adult skippers are strong,
fast fliers and can usually only be collected while they nectar at flowering plants. In southern
Florida, adults are usually first noticed in May with a second generation of adults appearing in
early June. It is not known how many generations per year occur in Florida but adults have been
collected in all months of the year (Kimball 1965) and all larval stages have been collected in
January. It is thought that C. ethlius can only overwinter in the very southernmost region of
Florida and must recolonize more northern regions each year (Moore 1928).
adult at rest
adult with wings spread
Female C. ethlius lay eggs singly or in widely spaced groups of five to seven eggs on the upper
and lower surfaces of canna leaves (Scudder 1889). The egg measures about 1.25 mm in
diameter and 0.68 mm in height. It is a pale green color when first deposited and, within a day,
becomes a distinct pink color (Moore 1928).
eggs
The first-instar larva ecloses after four to five days under Florida summer conditions and is
approximately 4 mm in length and yellowish in color (Scudder 1889, Cockerell 1892). Its head
is very large, black, glossy and bilobed. The thoracic shield, legs and anal tip are also black.
The larva consumes most of its egg shell (King 1880) and then moves to the margin of the leaf
where it eats two narrow strips from the margin of the leaf towards the midrib producing a leaf
flap (Moore 1928). The larva fastens silken strands between the outer edge of the leaf flap and
the main portion of the leaf. As the silk shrinks or condenses as it dries, the leaf flap is drawn
over the caterpillar, making a flattened tubular shelter with exits at either end. The larva keeps
the majority of its body within the leaf roll, only extending its head to feed. The leaf roll may
serve as both protection from predators and direct sun. The first instar molts to the next stage
after three days.
The remaining four larval instars range in length from 5 to 50 mm. The second through fourth
instars have a dark brown, almost black, head and a dark green body that is semi-transparent,
allowing the organs and tracheal system to be seen through the integument. The larvae appear
dark green because of the leaf material within their guts. There is a white stripe on each side of
the dorsum of the larva running the length of the body. The fifth instar has an orange head with a
dark triangle on the frontal region. The larvae consume most of the leaf around their leaf roll and
then move to another area of the leaf, when necessary. They roll a bigger leaf roll as they
outgrow the previous one. Several large larvae may defoliate an entire canna plant in this
manner. The larvae have an interesting behavior of flicking away frass so that their leaf roll
remains free of pellets and instead, frass accumulates on the ground. Fecal firing (see reference
below) is facilitated by the anatomy of the larva's anal comb and the buildup of hemostatic
pressure within its terminal abdominal segment (Caveney et al. 1998). It is hypothesized that
frass removal may reduce discovery by parasites and predators which often use the odor and
sight of frass as clues to the potential presence of hosts or prey.
second instar larva
fifth instar larva
The larva feeds voraciously during the final, fifth instar stage. As it prepares for pupation, the
larva ceases feeding and empties its gut of leaf material. It shortens in length and becomes bright
bluish green. This prepupal stage lasts from one to eight days in Florida, depending on the
ambient temperature (Moore 1928). The larva pupates within its leaf roll after first having spun
a thin silken mat covering the "floor" of its shelter. The chrysalis is bright green in color
(Cockerell 1892) and is approximately 36 mm in length (Scudder 1889). It has a pronounced
black spine at the anterior end and the long proboscis of the adult is enclosed in a case that
extends beyond the cremaster at the tip of the abdomen. The pupal stage lasts seven to eight
days in the summer in Florida.
larva before gut emptying
larva after gut emptying
pupa
pupa showing anterior spine
The host plants of C. ethlius include members of the Cannaceae family, which contains the single
genus, Canna. Calpodes ethlius has also been collected from West Indian arrowroot, Maranta
arundinacea L., of the closely-related family Marantaceae. Leaf rolling reduces the aesthetic
appeal of ornamental canna and voracious leaf feeding by larger larvae may be so severe that
plants do not flower (Young 1982). In food crops, such as arrowroot, severely defoliated plants
may produce little of the harvestable rhizome.
leaf damage
In 1981, 39 canna varieties were evaluated for host plant resistance to egg-laying (oviposition)
and larval feeding by C. ethlius (Reinert et al. 1983). In general, the red-leaved varieties
(especially 'Wyoming', 'Black Velvet', and 'Ambassador') received many more eggs than the
green-leaved varieties. Varieties with scarlet, red, or orange flowers, regardless of leaf color,
tended to experience more oviposition and larval feeding damage than varieties with other flower
colors. Although varieties have been identified that are particularly susceptible to the Brazilian
skipper, none has been identified as resistant.
Little attention has been paid to biological control of C. ethlius in ornamental canna. However,
this skipper attacks arrowroot, M. arundinacea, which is an important food crop in the Caribbean
region. A very small (0.8 to 1.2 mm in length) parasitic wasp, Ooencyrtus calpodicus Noyes
(Hymenoptera: Encyrtidae), was found in Trinidad attacking eggs of C. ethlius and was
introduced into other Caribbean islands for control of this species (Noyes 1985). Ooencyrtus
calpodicus has not been recorded from the United States, however. Three hymenopteran
parasites have been recorded from C. ethlius in Florida; Brachymeria incerta (Cresson)
(Chalicididae) parasitizing pupae and Xenufens ruskini Girault (Trichogrammatidae) (Krombein
et al. 1979) and Trichogramma minutum Riley (Trichogrammatidae) parasitizing eggs (Moore
1928). Parasitic tachinid flies, including Eucelatoria australis Townsend, Eusisyropa blanda
(Osten Sacken), and Lixophaga diatraeae (Townsend), have emerged from pupae in Florida
(Arnaud 1978). I have noted infection by pathogens which cause the larvae to turn black, liquify
and disintegrate. There is probably considerable natural mortality of C. ethlius in Florida due to
parasitism, predation, and diseases but obviously not enough to keep populations from heavily
defoliating cannas in certain years.
Chemical control is difficult because larvae are protected from direct chemical exposure within
their leaf rolls. If deemed necessary, chemical control should be attempted when larvae are small
and are still actively feeding on the leaves. Bacillus thuringiensis (Bt) products are probably the
best choice for chemical control. Follow the application instructions on the label of the specific
Bt product. Stickers will probably need to be added to the spray because the thick waxy coating
on canna leaves repels water. Other chemical insecticides are described in:
Insect Management Guide to landscape plants
Commercial Foliage and Woody Ornamental Arthropod Pest
Management
- Arnaud PH Jr. 1978. A Host-parasite Catalog of North American Tachinidae (Diptera). Miscellaneous
Publication No. 1319. USDA, Washington, D.C.
- Caveney S, McLean H, Surry D. (1998). Faecal firing in a skipper caterpillar is pressure-driven. The Journal of Experimental Biology 201: 121-133. (20 May 2000).
- Cockerell TDA. 1892. Notes on the life-history of Calpodes ethlius. Entomological News 3: 78-80.
- Kimball CP. 1965. The Lepidoptera of Florida: An annotated checklist. Division of Plant Industry, State of Florida Department of Agriculture, Gainesville, Florida.
- King HS. 1880. Internal organization of Hesperia ethlius Cram. as observed in the living animal. Pysche 3: 322-342.
- Krombein KV, Hurd PD Jr., Smith DR, Burks BD. 1979. Catalog of Hymenoptera in America north of Mexico. Vol. 1. Symphyta and Apocrita (Parasitica). Smithsonian Institution Press, Washington, D.C.
- Moore MB. 1928. A study of the life history and habits under Florida conditions of the canna butterfly (Brazilian skipper), Calpodes ethlius (Cramer), an insect pest of the canna. M.S. thesis, University of Florida, Gainesville. 95 p.
- Onore G, Mielke O. 1988. Calpodes ethlius (Cramer) (Lepidoptera, Hesperiidae) em Gal pagos. Rev. Bras. Zool. 5: 619-620.
- Opler PA, Pavulaan H, Stanford RE (coordinators). (1995). Butterflies of North America. Jamestown, ND: Northern Prairie Wildlife Research Center.
http://www.butterfliesandmoths.org/ (31 July 2007).
- Reinert JA, Broschat TK, Donselman HM. 1983. Resistance of Canna spp. to the
skipper butterfly, Calpodes ethlius (Lepidoptera: Hesperiidae). Environmental Entomology 12: 1829-
1832.
- Scudder SH. 1889. Calpodes ethlius - the Brazilian skipper, pp. 1750-1757. In The Butterflies
of the Eastern United States and Canada with Special Reference to New England. Vol. II
Lycaenidae, Papilionidae, Hesperidae. S. H. Scudder Publisher, Cambridge.
- Young AM. 1982. Notes on the interaction of the skipper butterfly Calpodes ethlius
(Lepidoptera: Hesperiidae) with its larval host plant Canna edulis (Cannaceae) in Mazatlan, state
of Sinaloa, Mexico. New York Entomological Society 90: 99-114.
Author: Heather J. McAuslane, University of Florida, and Kim King, University of Western Ontario, London, Ontario, Canada
Photographs: Paul M. Choate, University of Florida and Kim King, University of Western Ontario, London, Ontario, Canada
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-132
Publication Date: May 2000. Latest revision: July 2007.
Copyright 2000-2007 University of Florida
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