common name: yellowstriped armyworm
scientific name: Spodoptera ornithogalli (Guenée) (Insecta: Lepidoptera: Noctuidae)
The yellowstriped armyworm, Spodoptera ornithogalli (Guenée), is common in the eastern United States
as far west as the Rocky Mountains, and occurs in southern Canada. However, it also is reported from
southwestern states, including California. The distribution of this native insect includes Mexico, Central
and South America, and many Caribbean islands. As a pest, however, its occurrence is limited
principally to the southeastern states. A very similar species, western yellowstriped armyworm,
Spodoptera praefica (Grote), is known only from the western states, principally California and
Oregon. In California, S. praefica is much more important than S. ornithogalli.
yellowstriped armyworm
western striped armyworm
There apparently are three to four generations annually, with broods of adults present in March to
May, May to June, July to August, and August to November. Some of the latter brood of
yellowstriped overwinter as pupae rather than emerging as adults. Although eggs, larvae and adults of
yellowstriped armyworm may be present in autumn or early winter they cannot withstand cold weather,
and perish. Development time, from egg to adult, is about 40 days.
Eggs: The eggs are greenish to pinkish brown in color and bear 45 to 58 small ridges. In shape, the
egg is a slightly flattened sphere, measuring 0.46 to 0.52 mm in diameter and 0.38 to 0.40 mm in height.
Females typically deposit clusters of 200 to 500 eggs, usually on the underside of leaves. Total
fecundity was determined to be over 3000 eggs under laboratory conditions. The eggs are covered
with scales from the body of the adults. Duration of the egg stage is three to five days at warm
temperatures.
Larvae: Larvae initially are gregarious in behavior, but as they mature they disperse, sometimes
spinning strands of silk upon which they are blown by the wind. There usually are six instars, although
seven instars have been reported. Head capsule widths are about 0.28, 0.45, 0.8-1.0, 1.4-1.6, 2.0-
2.2, and 2.8-3.0 mm, respectively, for instars one through 6. The larva grows from about 2.0 to 35
mm in length over the course of development. Coloration is variable, but mature larvae tend to bear a
broad brownish band dorsally, with a faint white line at the center. More pronounced are black
triangular markings along each side, with a distinct yellow or white line below. A dark line runs laterally
through the area of the spiracles, and below this is a pink or orange band.
dorsal view of larva
Dark subdorsal spots are found on the mesothorax of yellowstriped armyworm, and the triangular
shape of these spots aids in distinguishing this insect from sweetpotato armyworm, Spodoptera
dolichos, and velvet armyworm, S. latifascia, in eastern states. The head is brown but has extensive
blackish markings. Duration of the larval stage is 14 to 20 days, with the first three instars requiring
about two days each and the last three instars requiring about three days each.
Pupae: Larvae pupate in the soil within a cell containing a thin lining of silk. The reddish brown pupa
measures about 18 mm in length. Duration of the pupal stage is nine to 22 days, normally averaging 12
to 18 days.
Adults: The moths measure 34 to 41 mm in wing span. The front wings are brownish gray with a
complicated pattern of light and dark markings. Irregular whitish bands normally occur diagonally near
the center of the wings, with additional white coloration distally near the margin. The hind wings are
opalescent white, with a narrow brown margin. Under laboratory conditions average longevity of adults
is 17 days, with most egg production completed by the tenth day (Adler et al. 1991).
adult
The most complete description of S. ornithogalli and its biology is given by Crumb (1929), with
additional comments by Crumb (1956). Keys for identification are also found in these references.
Keys for separation of Spodoptera adults can be found in Todd and Poole (1980) and Heppner
(1998) Larvae can be distinguished using the keys of Passoa (1991) and Heppner (1998). Rearing on
artificial diet is described by Adler and Adler (1988).
Larvae damage plants principally by consumption of foliage. The small, gregarious larvae tend to
skeletonize foliage but as the larvae grow and disperse they consume irregular patches of foliage or
entire leaves. However, they will also feed on the fruits of tomato, cotton, and other plants. Larval
consumption of soybean was estimated by King (1981) to total 115 sq cm; this is an intermediate value
relative to some other lepidopterous defoliators.
These species are very general feeders, reportedly damaging many crops. Among vegetable crops
injured are asparagus, bean, beet, cabbage, cantaloupe, carrot, corn, cucumber, lettuce, onion, pea,
potato, rhubarb, rutabaga, salsify, sweet potato, tomato, turnip, and watermelon. Other crops
damaged include alfalfa, blackberry, cotton, clover, grape, lentil, peach, rape, raspberry, sorghum,
soybean, sugarbeet, sweetclover, sunflower, tobacco, wheat, and several flower crops. Some of the
weed species known to be suitable hosts are castorbean, Ricinus communis; dock, Rumex sp.;
gumweed, Grindelia sp.; horse nettle, Solanum carolinense; horseweed, Erigeron canadensis;
jimsonweed, Datura sp.; lambsquarters, Chenopodium album; morningglory, Ipomoea sp.; plantain,
Plantago lanceolata; prickly lettuce, Lactuca scariola; and redroot pigweed, Amaranthus
retroflexus. In many cases, yellowstriped armyworm develops first on weed or rangeland plants, with
subsequent generations affecting crops.
Several wasp parasitoids affect S. ornithogalli, including Rogas laphygmae Viereck, R. terminalis (Cresson), Zele mellea (Cresson), Chelonus insularis Cresson and Apanteles griffini Viereck (all Hymenoptera: Braconidae). Also, Euplectrus plathypenae Howard (Hymenoptera: Eulophidae) attacks larvae and causes a cessation of feeding within two days (Parkman and Shepard 1981). Thus,
this parasitoid is particularly valuable at minimizing damage.
Numerous flies have been found to parasitize yellowstriped armyworm including Archytas spp.,
Choeteprosopa hedemanni Brauer and Bergenstamm, Euphorocera omissa (Reinhard), E.
tachinomoides Townsend, Lespesia aletiae (Riley), L. archippivora (Riley), Omotoma fumiferanae (Tothill), Winthemia quadripustulata (Fabricius), and W. rufopicta (Bigot) (all Diptera: Tachinidae).
A nuclear polyhedrosis virus is highly pathogenic to larvae, and survivors that do not succumb exhibit
reduced fecundity (Hostetter et al. 1990, Young 1990).
Undoubtedly predators are important, but their effect has not been quantified. In the related western
yellowstriped armyworm. Bisabri-Ershadi and Ehler (1981) reported that over 96% of total mortality
occurred in the egg and early larval stages, and most was attributed to predation. The most important
predators were minute pirate bug, Orius tristicolor (White) (Hemiptera: Anthocoridae); bigeyed bugs,
Geocoris spp. (Hemiptera: Lygaeidae); and damsel bugs, Nabis spp. (Hemiptera: Nabidae). The
legume bug, Lygus hesperus Knight (Hemiptera: Miridae), was a facultative predator, often feeding on
armyworm eggs. These, or similar, predators undoubtedly affect yellowstriped armyworm.
damsel bug
Chemical control. Insecticides are applied to foliage to prevent injury by larvae. The microbial insecticide
Bacillus thuringiensis can be applied to kill armyworms, but should be applied when the larvae are
young, as they become difficult to control as they mature. Larvae will consume bran bait containing
insecticide.
Insect Management Guide for field crops
Insect Management Guide for vegetables
Cultural control. Proximity of crops to rangeland containing weed hosts, or to alfalfa, may be
important factors predisposing vegetable crops to injury. At high densities, especially if alfalfa hay is
mowed, larvae will sometime disperse simultaneously and invade nearby vegetable fields. Physical
barriers such as trenches can be used to deter such dispersal.
- Adler PH, Adler CRL. 1988. Behavioral time budget for larvae of Heliothis zea
(Lepidoptera: Noctuidae) on artificial diet. Annals of the Entomological Society of America 81: 682-688.
- Adler PH, Willey MB, Bowen MR. 1991. Temporal oviposition patterns of Heliothis zea
and Spodoptera ornithogalli. Entomologica Experimentalis et Appliciata 58: 159-164.
- Bisabri-Ershadi B, Ehler LE. 1981. Natural biological control of western yellow-striped
armyworm, Spodoptera praefica (Grote), in hay alfalfa in northern California. Hilgardia 49: 1-23.
- Capinera JL. 2001. Handbook of Vegetable Pests. Academic Press, San Diego. 729 pp.
- Crumb SE. 1929. Tobacco cutworms. U.S. Department of Agriculture Technical Bulletin 88. 179 pp.
- Crumb SE. 1956. The larvae of the Phalaenidae. U.S. Department of Agriculture Technical Bulletin 1135. 356 pp.
- Heppner JB. 1998. Spodoptera armyworms in Florida (Lepidoptera: Noctuidae). Florida Department of Agriculture and Consumer Services, Division of Plant Industry Entomology Circular 390. 5pp.
- Hostetter DL, Puttler B, McIntosh AH, Pinnell RE. 1990. A nuclear polyhedrosis virus of
the yellowstriped armyworm (Lepidoptera: Noctuidae). Environmental Entomology 19: 1150-1154.
- King EW. 1981. Rates of feeding by four lepidopterous defoliators of soybeans. Journal of the Georgia Entomological Society 16: 283-288.
- Parkman P, Shepard M. 1981. Foliage consumption by yellowstriped armyworm larvae after
parasitization by Euplectrus plathypenae. Florida Entomologist 64: 192-194.
- Passoa S. 1991. Color identification of economically important Spodoptera larvae in Honduras
(Lepidoptera: Noctuidae). Insecta Munda 5: 185-196.
- Todd EL, Poole RW. 1980. Keys and illustrations for the armyworm moths of the noctuid
genus Spodoptera Guenée from the Western Hemisphere. Annals of the Entomological Society of America 73: 722-738.
- Wilkerson JL, Webb SE, Capinera JL. (2005). Vegetable Pests III: Lepidoptera. UF/IFAS CD-ROM. SW 182.
- Young SY. 1990. Effect of nuclear polyhedrosis virus infection in Spodoptera ornithogalli larvae on
post larval stages and dissemination by adults. Journal of Invertebrate Pathology 55: 69-75.
Author: John L. Capinera, University of
Florida
Photographs: John L. Capinera, University of Florida; and Ken Gray, Oregon State University
Project Coordinator: Thomas Fasulo, University of Florida
Publication Number: EENY- 216
Publication Date: July 2001. Revised November 2005.
Copyright 2001-2005 University of Florida
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Department of Entomology and Nematology
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