LepIntercept

NOCTUIDAE - S. frugiperda (J. E. Smith) Non-Rep

Taxonomy

Noctuoidea: Noctuidae: Noctuinae: Spodoptera frugiperda (J. E. Smith)

Common names: fall armyworm, cogollero, whorlworm, corn leafworm, southern grassworm

Synonyms: Laphygma frugiperda

Larval diagnosis (Summary)

Characteristic body coloration (see Figs. 1-3 and Detailed Information)
Dorsal pinacula of A1-8 are larger than the diameter of the corresponding spiracle
Minute sclerotized bar connecting the SD1 setal base to a tonofibrillary platelet on the meso- and metathorax
Cuticle with granulose texture

Host/origin information

Larvae of S. frugiperda are routinely intercepted from locations in Central and South America on a variety of hosts. The most common origin is Mexico, accounting for 65% of all records. Other common origin/host combinations are listed here:

Origin Host(s)

Colombia Alstroemeria, Chrysanthemum, Gerbera

Dominican Republic Capsicum

Mexico Apium, Brassica, Capsicum, Gladiolus, Ocimum, Zea mays

Recorded distribution

Spodoptera frugiperda is widely distributed throughout North, Central, and South America. It is also present in the Caribbean (Pogue 2002).

Identification authority (Summary)

Spodoptera frugiperda is highly polyphagous, thus host data often does not help identification. Origin data is useful because this species does not naturally occur outside of the New World. The morphological characters listed here should be sufficient to identify S. frugiperda to species, even in early instars.

Pest characterization

(Based on Cavey 2001, Pogue 2002)

Taxonomy: High. Species identification is often possible.
Distribution: Low. Spodoptera frugiperda is present in the U.S.
Potential Impact: High. Spodoptera frugiperda is a pest species.

This ranking characterizes S. frugiperda as not quarantine significant for the U.S.

NOCTUIDAE - S. frugiperda (J. E. Smith) Non-Rep

Larval diagnosis (Detailed)

The larva of the fall armyworm, Spodoptera frugiperda, was at least partially described by Luginbill (1928), Crumb (1956), Etcheverry (1957), Okumura (1961), Peterson (1962), Dekle (1976), Pastrana and Henandez (1979), Passoa (1991), and Pogue (2002). The larva has been photographed many times; some examples are Passoa (1991), Pogue (2002), and Wagner et al. (2011).

Typical interceptions of S. frugiperda are immediately recognized by their characteristic appearance. The ground color is normally some shade of brown or gray, more rarely the larva is light green or almost black. The dorsal pinacula of A1-8 are large, greater than the diameter of the corresponding spiracle (Levy and Habeck 1976), and especially conspicuous on last few abdominal segments where they form a square on A8 (Dekle 1976). Some individuals do not have the lateral spot on A1 typical of most other Spodoptera. However, there is a minute sclerotized bar connecting the SD1 setal base to an adjacent ventral muscle attachment (tonofibrillary platelet) on the meso- and metathorax (Weisman 1974, 1986; Passoa 1991) which is typical of the genus (and many other noctuids; see S. exigua). Spodoptera frugiperda has SD1 is hairlike on the mesothorax, metathorax, and A9. The blade on the hypophargngeal complex is a long ridge in our example, much like the example in Passoa (1991: fig. 7) but shorter. We show a rare form of S. frugiperda with dashes on the dorsum, normally these are absent (see Passoa 1991, Pogue 2002, Wagner et al. 2011).

Some green forms of S. frugiperda resemble S. exigua if the pinacula are very pale (Passoa 1991). Crumb (1956) separated these two species, in part, by the position of a line connecting the P1 setae on the head. The line is above the apex of the front in S. frugiperda but below the apex in S. exigua (see illustrations in Okumura 1961). The cuticle has flat granulose texture (Passoa 1991: fig. 4, Pastrana and Henandez 1979: fig. 128). No other Spodoptera species studied by Pogue (2002) has the combination of large pinacula and granulose skin.

Identification authority (Detailed)

Spodoptera frugiperda is highly polyphagous, thus host data often does not help identification. The recorded distribution includes almost the entire New World (Pogue 2002), but S. frugiperda does not naturally occur in the Old World. Early instar larvae that show the spot on A1, the large pinacula and the granulose texture can be identified as S. frugiperda.

NOCTUIDAE - S. frugiperda (J. E. Smith) Non-Rep

Origin records

S. frugiperda has been intercepted from the following locations:

Argentina, Barbados, Belize, Brazil, Canada, China, Colombia, Costa Rica, Dominica, Dominican Republic, Ecuador, Guatemala, Guyana, Haiti, Honduras, Indonesia, Israel, Jamaica, Mexico, Micronesia, Netherlands, Nicaragua, Panama, Peru, Puerto Rico, Thailand, Trinidad and Tobago, Turkey, Venezuela

Records from China, Indonesia, Israel, Micronesia, the Netherlands and Thailand require confirmation.

Host records

S. frugiperda has been intercepted on the following hosts:

Abelmoschus esculentus, Abelmoschus sp., Allium cepa, Allium porrum, Allium schoenoprasum, Allium sp., Alstroemeria sp., Amaranthus sp., Ananas comosus, Ananas sp., Anethum graveolens, Anethum sp., Apiaceae, Apium graveolens, Apium graveolens var. dulce, Apium sp., Artemisia dracunculus, Artemisia sp., Asparagus officinalis, Asparagus sp., Aster sp., Asteraceae, Basilicum sp., Beta vulgaris var. cicla, Brassica campestris, Brassica chinensis, Brassica juncea, Brassica oleracea, Brassica oleracea var. botrytis, Brassica oleracea var. capitata, Brassica oleracea var. italica, Brassica pekinensis, Brassica rapa, Brassica rapa ssp. chinensis, Brassica rapa ssp. pekinensis, Brassica sp., Brassicaceae, Bromelia sp., Callistephus chinensis, Callistephus sp., Capsicum annuum, Capsicum frutescens, Capsicum sinense, Capsicum sp., Carica papaya, Carya sp., Celosia sp., Chenopodium berlandieri ssp. nuttalliae, Chenopodium berlandieri ssp. nuttalliae, Chrysanthemum sp., Cicer arietinum, Cichorium endivia, Citrullus lanatus, Citrus aurantiifolia, Codiaeum sp., Cordyline sp., Coriandrum sativum, Cucurbita sp., Cymbidium sp., Cymbopogon citratus, Cynara cardunculus, Cynara scolymus, Cyperus papyrus, Dianthus sp., Diospyros sp., Dysphania ambrosioides, Eruca vesicaria, Eryngium foetidum, Eryngium sp., Fabaceae, Fragaria ananassa, Fragaria sp., Gerbera sp., Gladiolus sp., Gypsophila sp., Helianthus annuus, Helianthus sp., Heliconia sp., Hydrangea sp., Hypericum sp., Iris sp., Lablab sp., Lactuca sativa, Lactuca sp., Lagenaria siceraria, Lamiaceae, Leucaena sp., Lilium sp., Limonium sp., Lycopersicon sp., Mangifera indica, Manihot esculenta, Maranta leuconeura, Maranta sp., Matthiola sp., Mazus sp., Melicoccus bijugatus, Mentha arvensis, Mentha sachalinensis, Mentha sp., Moluccella laevis, Molucella sp., Momordica charantia, Momordica sp., Musa paradisiaca, Musa sp., Ocimum basilicum, Ocimum sp., Opuntia sp., Origanum majorana, Origanum sp., Origanum vulgare, Penstemon sp., Persea americana, Petroselinum crispum, Phaseolus sp., Phaseolus vulgaris, Phormium sp., Physalis philadelphica, Physalis pubescens, Physalis sp., Piper sp., Pisum sativum, Pisum sativum var. macrocarpon, Pisum sp., Poaceae, Prosopis sp., Punica granatum, Ranunculus sp., Raphanus sp., Rosa sp., Rosaceae, Rosmarinus officinalis, Rubus sp., Rubus ursinus, Rumohra sp., Saccharum officinarum, Salvia officinalis, Salvia sp., Sechium edule, Setaria italica, Setaria sp., Solanum integrifolium, Solanum lycopersicum var lycopersicum, Solanum melongena, Solanum sp., Solidago sp., Spinacia oleracea, Strelitzia sp., Stromanthe sp., Tagetes lucida, Tagetes sp., Theobroma cacao, Thymus sp., Thymus vulgaris, Tulipa sp., Vaccinium corymbosum, Vaccinium sp., Vigna sp., Yucca sp., Zantedeschia sp., Zea mays, Zea sp., Zingiber officinale, Zizania sp.