Noctuoidea: Noctuidae: Heliothinae: Helicoverpa
earworms, bollworms
Various species have been previously placed in Heliothis.
Helicoverpa is a worldwide genus consisting of 20 described species (Matthews 1999Matthews 1999:
Matthews, M. 1999. Heliothine moths of Australia: a guide to pest bollworms and related noctuid groups. Monographs on Australian Lepidoptera Series 7. Commonwealth Scientific and Industrial Research Organisation. Melbourne, Australia. 320 pp.). Hardwick (1965: 28) suggested a few larval characters that will diagnose Helicoverpa from other members of the Heliothinae (including Heliothis, Chloridea, etc.). Identification to species relies on other morphological characters in addition to body markings, origin, and host. Usually only middle to late instar larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
can be identified below the subfamily level.
The two most frequently intercepted Helicoverpa include: H. armigera and H. zea. Diagnoses for these two species are provided on the respective fact sheets along with keys to separate them from other Helicoverpa. No morphological characters have been identified that will consistently separate the larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
of H. armigera from those of H. zea.
Morphological characters to distinguish larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
of the Heliothinae including Helicoverpa (modified from Hardwick 1965Hardwick 1965:
Hardwick, D. F. 1965. The corn earworm complex. Memoirs of the Entomological Society of Canada 40: 1-247.) include:
Because Helicoverpa is a worldwide genus with many polyphagous species, larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
can be intercepted from nearly any origin on most any host. A complete list of the host and origin data for "Helicoverpa spp." is listed on the Interception Records tab. Common host/origin combinations for the two most frequently intercepted species of Helicoverpa (H. armigera and H. zea) are provided on the respective fact sheets.
Helicoverpa is a worldwide genus (Hardwick 1965Hardwick 1965:
Hardwick, D. F. 1965. The corn earworm complex. Memoirs of the Entomological Society of Canada 40: 1-247.).
Species identification of late instarinstar:
the stage between molts
larval Heliothinae can be found in the Heliothinae and H. armigera keys (below) and on the fact sheets for H. zea and H. armigera. Examples are given when identification to species, genus, or only subfamily is appropriate. This discussion focuses on identification of the early instars to genus.
Helicoverpa larvae change color and form during development (Hardwick 1965Hardwick 1965:
Hardwick, D. F. 1965. The corn earworm complex. Memoirs of the Entomological Society of Canada 40: 1-247.). Early instars, as shown on the fact sheet for H. armigera, have dark pinaculapinaculum:
a small, flat, or slightly elevated chitinized area bearing a seta or setae
and a faint or absent pattern of stripes or lines. Later instars develop the color pattern typical of the genus. Besides H. armigera, another good example of this developmental change is in H. assulta; the early instarinstar:
the stage between molts
is pictured here in PaDIL (click for link). Li et al. (2013)Li et al. (2013):
Li, H., H. Zhang, R. Guan and X. Miao. 2013. Identification of differential expression genes associated with host selection and adaptation between two sibling insect species by transcriptional profile analysis. Biomedical Central Genomics 14: 582. illustrated the mature larvalarva:
the stages between the egg and pupa of those insects having complete metamorphosis
.
According to Neunzig (1969)Neunzig (1969):
Neunzig, H. H. 1969. The biology of the tobacco budworm and the corn earworm in North Carolina with particular reference to tobacco as a host. North Carolina Agricultural Experiment Station Technical Bulletin 196. 76 pp., based on H. zea, the pinaculapinaculum:
a small, flat, or slightly elevated chitinized area bearing a seta or setae
and microspine character for recognizing Helicoverpa works only on the third to last instarinstar:
the stage between molts
. It cannot be used on early instars. Like the later instars, early instars of Helicoverpa never have a large retinaculumretinaculum:
a projection or toothlike structure on the oral surface of the mandible
.
It is easy to confuse early instar larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
of Helicoverpa with those noctuids that have a spiny or finely granular cuticle. Heliothinae do not have stout setaeseta:
a hairlike projection of the body wall that is articulated in a socket; compare to spine
with a blunt tip or faint club as is common in many Herminiinae (see illustrations in Wagner et al. 2011Wagner et al. 2011:
Wagner, D. L., D. F. Schweitzer, J. B. Sullivan and R. C. Reardon. 2011. Owlet caterpillars of eastern North America. Princeton University Press, New Jersey. 576 pp.).
Identification of Helicoverpa in the early instars is sometimes justified. Below are a few of some of these situations (not a complete list):
1. The host or origin suggests that only one species present in the pathway and the larvalarva:
the stages between the egg and pupa of those insects having complete metamorphosis
is consistent with the Helicoverpa early instarinstar:
the stage between molts
description. An example would be H. zea in corn ears from Mexico and Central America.
2. The origin can rule out sibling species. For example, Hawaii has several Helicoverpa species but only C. virescens. The keys to first, second and third, and third to last instars in Neunzig (1969)Neunzig (1969):
Neunzig, H. H. 1969. The biology of the tobacco budworm and the corn earworm in North Carolina with particular reference to tobacco as a host. North Carolina Agricultural Experiment Station Technical Bulletin 196. 76 pp. could be used to separate H. zea (and the native Helicoverpa species more than likely) from C. virescens.
3. The larvalarva:
the stages between the egg and pupa of those insects having complete metamorphosis
is clearly a middle instar Helicoverpa, but poorly known rare species prevent recognition of the common pests forcing only a generic identification. Helicoverpa sugii has a restricted distribution in Japan and an unknown host range (Yoshimatsu and Takeuchi 2004Yoshimatsu and Takeuchi 2004:
Yoshimatsu, S. and K. Takeuchi. 2004. Description of Helicoverpa sugii sp. nov. (Lepidoptera: Noctuidae: Heliothinae) from the Ogasawara (Bonin) Islands, Japan, with brief biological notes. Transactions of the Lepidoptera Society of Japan 55: 34-38.). Species identification of Helicoverpa in Australia by morphology is difficult to impossible.
Do not identify a larvalarva:
the stages between the egg and pupa of those insects having complete metamorphosis
as Helicoverpa if a large retinaculumretinaculum:
a projection or toothlike structure on the oral surface of the mandible
is present, the dorsal pinaculapinaculum:
a small, flat, or slightly elevated chitinized area bearing a seta or setae
have microspinesmicrospines:
minute spines on the body, usually visible only under magnification
near the top of the setal base, or the body setaeseta:
a hairlike projection of the body wall that is articulated in a socket; compare to spine
are stout with a faint club or blunt tip. Helicoverpa fletcheri from Africa is an exception.
The vast majority of early instarinstar:
the stage between molts
Heliothinae are best left at subfamily with the notation that the larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
are too young to name with morphology.
NOTE: Due to the continuing spread of H. armigera in South America, exercise caution when attempting identifications from that continent. There are no morphological characters to separate the larvaelarva:
the stages between the egg and pupa of those insects having complete metamorphosis
of H. armigera from H. zea. When in doubt, default to "Helicoverpa sp." instead of attempting a species-level ID. The following keys may not reflect the most recent H. armigera distribution in South America.
Identification guide to larval Heliothinae (Lepidoptera: Noctuidae) of quarantine significance
Key to the identification of Helicoverpa armigera suspects intercepted at U.S. ports of entry
Helicoverpa have been intercepted from the following locations:
Afghanistan, Angola, Australia, Austria, Azores, Bangladesh, Benin, Brazil, Bulgaria, Cambodia, Cameroon, Canada (?), Cape Verde, China, Colombia, Congo, Costa Rica, Cote D'Ivoire, Czech Republic, Dominican Republic, Ecuador, Egypt, El Salvador, Fiji, France, Gambia, Germany, Ghana, Greece, Guatemala, Guinea, Guyana, Haiti, Hong Kong, India, Indonesia, Iran, Israel, Italy, Jamaica, Japan, Jordan, Kenya, Laos, Lebanon, Lithuania, Macao, Macedonia, Malaysia, Mali, Mexico, Morocco, Nepal, Netherlands, New Zealand, Nigeria, Norway (?), Pakistan, Palestinian Territory, Peru, Philippines, Portugal, Puerto Rico, Romania, Saudi Arabia, Senegal, Serbia, Serbia and Montenegro, Singapore, South Africa, South Korea, Spain, Syrian Arab Republic, Tanzania, Thailand, Togo, Trinidad and Tobago, Tunisia, Turkey, United Kingdom of Great Britain and N. Ireland, Uzbekistan, Venezuela, Viet Nam, Zambia, Zimbabwe
Helicoverpa have been intercepted on the following hosts:
Abelmoschus esculentus, Abelmoschus sp., Achillea sp., Aconitum sp., Agapanthus sp., Ageratum sp., Alcea rosea, Alchemilla mollis, Alchemilla sp., Allium porrum, Allium schoenoprasum, Allium sp., Alstroemeria sp., Amaranthus sp., Ammi majus, Ammi sp., Ananas comosus, Anemone coronaria, Anemone nemorosa, Anemone sp., Anethum graveolens, Anigozanthus sp., Annona sp., Anthemis sp., Anthriscus cerefolium, Antirrhinum sp., Apium graveolens, Artemisia dracunculus, Artemisia sp., Asclepias sp., Asclepias tuberosa, Asparagus officinalis, Aster sp., Astilbe sp., Astrantia sp., Berzelia sp., Bouvardia sp., Brassica sp., Brunia albiflora, Bupleurum griffithii, Bupleurum sp., Cajanus cajan, Calendula sp., Calla sp., Campanula glomerata, Campanula sp., Capsicum annuum, Capsicum pubescens, Capsicum sp., Carthamus sp., Celosia argentea, Celosia sp., Cestrum sp., Chamelaucium sp., Chenopodiaceae, Chenopodium sp., Chichorium sp., Chrysanthemum sp., Cicer arietinum, Cicer sp., Cichorium intybus, Cichorium sp., Citrus hystrix, Clematis sp., Colocasia esculenta, Corchorus sp., Coriandrum sativum, Coridothymus capitatus, Crossandra sp., Crotalaria sp., Cucurbita pepo, Cucurbita sp., Cucurbitaceae, Cymbidium sp., Cynara sp., Dahlia sp., Delphinium sp., Dendranthema sp., Dendrobium sp., Dianthus caryophyllus, Dianthus sp., Diascia sp., Dimocarpus sp., Dolichos sp., Echinacea sp., Eremurus sp., Ergngium sp., Erica sp., Eruca sativa, Eruca vesicaria, Eryngium sp., Euphorbia sp., Eustoma grandiflorum, Eustoma sp., Fabaceae, Fragaria sp., Gardenia jasminoides, Gardenia sp., Genista sp., Gentiana sp., Gerbera sp., Gladiolus sp., Glycine max, Gomphrena globosa, Gomphrena sp., Gravilea sp., Grevillea sp., Gypsophila sp., Helianthus annuus, Helianthus sp., Helleborus sp., Hibiscus sp., Hydrangea sp., Hypericum sp., Ixora sp., Jasminum sambac, Jasminum sp., Lablab purpureus, Lablab sp., Lactuca sativa, Lavandula sp., Leucadendron platyspermum, Leucadendron sp., Leucospermum cordifolium, Leucospermum sp., Liatris sp., Lilium sp., Limonium perezii, Limonium sp., Lippia sp., Lisianthus sp., Lycopersicon esculentum, Lycopersicon sp., Lysimachia sp., Marjorana hortensis, Matricaria sp., Mentha arvensis, Mentha longifolia, Mentha sp., Mentha spicata, Moluccella sp., Momordica balsamina, Monstera sp., Musa sp., Nasturtium sp., Nelumbium sp., Nelumbo nucifera, Nerine sp., Nigella sp., Ocimum basilicum, Ocimum sp., Oncidium sp., Orchidaceae, Origanum majorana, Origanum sp., Origanum vulgare, Ornithogalum arabicum, Ornithogalum orabiaum, Ornithogalum sp., Oryza sativa, Paeonia sp., Papaver sp., Paullinia sp., Persea americana, Petroselinum crispum, Petunia sp., Phaseolus sp., Phaseolus vulgaris, Phlox sp., Photinia sp., Physalis ixocarpa, Physalis philadelphica, Physalis sp., Pieris sp., Pisum sativum, Pisum sativum var. macrocarpon, Pisum sp., Pittosporum sp., Plectranthus sp., Poaceae, Polianthes tuberosa, Polyanthus sp., Protea sp., Prunus sp., Psidium guajava, Ranunculaceae, Ranunculus asiaticus, Ranunculus sp., Raphanus sativus, Rosa sp., Rosmarinus officinalis, Rosmarinus sp., Rudbeckia sp., Rumex acetosa, Salvia officinalis, Salvia sp., Sarcocaulon sp., Satureja hortensis, Scabiosa sp., Sedum sp., Serruria sp., Setaria italica, Solanaceae, Solanum aethiopicum, Solanum lycopersicum var lycopersicum, Solanum melongena, Solanum sp., Solidago sp., Symphoricarpos sp., Syringa sp., Tagetes erecta, Tagetes sp., Thymus citriodorus, Thymus sp., Thymus vulgaris, Trachelium sp., Tulipa sp., Veronica longifolia, Veronica sp., Veronica spicata, Verticordia sp., Viburnum sp., Vicia faba, Zantedeschia sp., Zea mays, Zea sp.
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