Automeris io

Last updated

Io moth
Automeris ioFMPCCA20040704-2974B1.jpg
Female (top) and male (below)
Status TNC G5.svg
Secure  (NatureServe) [1]
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Family: Saturniidae
Genus: Automeris
Species:
A. io
Binomial name
Automeris io
(Fabricius, 1775) [2]
Subspecies [3]
  • Automeris io io(Fabricius, 1775)
  • Automeris io neomexicanaBarnes & Benjamin, 1923
Synonyms [4]
  • Bombyx ioFabricius, 1775
  • Phalaena io(Fabricius, 1775)
  • Hyperchiria io(Fabricius, 1775)
  • Hyperchiria lilithStrecker, 1872

Automeris io, the Io moth (EYE-oh) or peacock moth, is a colorful North American moth in the family Saturniidae. [5] [6] The Io moth is also a member of the subfamily Hemileucinae. [7] The name Io comes from Greek mythology in which Io was a mortal lover of Zeus. [8] The Io moth ranges from the southeast corner of Manitoba and in the southern extremes of Ontario, Quebec, New Brunswick and Nova Scotia in Canada, and in the US it is found from Montana, North Dakota, South Dakota, Nebraska, Colorado, New Mexico, Texas, Utah, east of those states and down to the southern end of Florida. [9] The species was first described by Johan Christian Fabricius in 1775.

Contents

Adult description

Adult male Io moth - 7746 - Automeris io - Io Moth (27522147070).jpg
Adult male Io moth

Imagines (sexually mature, reproductive stage) have a wingspan of 2.5–3.5 inches (63–88 mm). [7] [9] This species is sexually dimorphic: males have bright yellow forewings, body, and legs, while females have reddish-brown to purple forewings, body, and legs. [4] [10] The males also have much bigger plumose (feathery) antennae than the females. [4] Both males and females have one big black to bluish eyespot with some white in the center, on each hindwing. [10] [11] [12] Some hybridizations have resulted in variations in these hindwing eyespots. [11] [12] Adults live 1–2 weeks.

Eyespots on a female moth - 7746 - Automeris io - Io Moth (47990121411).jpg
Eyespots on a female moth

Parasitoids

Many species of flies (Tachinidae) and wasps (Ichneumonidae and Braconidae) are known parasitoids. [4] The flies include the introduced Compsilura concinnata , Lespesia sabroskyi , Chetogena claripennis , Carcelia formosa , Sisyropa eudryae , Lespesia frenchii , and Nilea dimmocki . [13] The wasps include the Ichneumonidae species Hyposoter fugitivus and Enicospilus americanus , [4] and the Braconidae species Cotesia electrae and Cotesia hemileucae . [4]

Predators

Io moths have many predators. These include birds, small mammals, and spiders. [4] [10]

Defenses

Stinging spines of caterpillar Io moths have a very painful venom that is released with the slightest touch. There are two hypotheses regarding where this venom originates: (1) the glandular cells on the base of the branched seta or (2) from the secretory epithelial cells. [14] Contacting the seta is not life-threatening for humans, but still causes irritation to the dermal tissue, resulting in an acute dermatitis called erucism. [15] [16] Both male and female adult io moths utilize their hindwing eyespots in predatory defense when the moth is sitting in the head-down position or is touched, via shaking and exposing these eyespots. [11] [12] [10]

Life cycle

Females lay small, white ova in the leaves of host plants, including:

First instar on Quercus virginiana Automeris io 1st instar 1 sjh.JPG
First instar on Quercus virginiana
Final instar Io moth caterpillar Io moth caterpillar.png
Final instar Io moth caterpillar

The eggs have large micropyle rosettes that turn black as the fertile eggs develop. They are usually laid in clusters of more than twenty and hatch within 8–11 days. [4] [10] From the eggs, orange larvae emerge, usually eating their egg shell soon after hatching. [4] They go through five instars, each one being a little different.

Female Io moth after laying eggs Io moth after laying eggs.JPG
Female Io moth after laying eggs

The caterpillars are herbivorous and gregarious in all their instars, and may be seen traveling in single-file processions over the food plant. [10] [19] [7] As the larvae develop, they will lose their orange color and will turn bright green and urticating, having many spines. The green caterpillars have two lateral stripes, the upper one being bright red and the lower one being white. These caterpillars can reach sizes of 7 cm in length. [20] When the caterpillars are ready, they spin a flimsy, valveless cocoon made from a dark, coarse silk. Some larvae will crawl to the base of the tree and make their cocoons among leaf litter on the ground, while others will use living leaves to wrap their cocoons with. [4] [7] The leaves will turn brown and fall to the ground during fall, taking the cocoons with them. [4] [7] There they pupate, the pupa being dark brown/black. [4] The pupae also have sexual dimorphism with the females' possessing a notch on their posterior ventral aspect, while the males' pupae bear a pair of tubercles near that area with no notch. [4]

Automeris io caterpillars on reed (Automeris io) caterpillars on reed.jpg
Automeris io caterpillars on reed

Adult Io moths normally emerge from their cocoons in late morning or early afternoon. The emergence of the adults moths is typically from June to July. [21] Eclosion (emergence from the cocoon) only takes a few minutes. [19] After eclosing, the moths climb and hang on plants so that their furled wings can be inflated with fluid (hemolymph) pumped from the body. This inflation process takes about twenty minutes. Adult moths are strictly nocturnal, generally flying during the peak hours of the night. [21] The females generally wait until nightfall and then extend a scent gland from the posterior region of the abdomen, in order to attract males via wind-borne pheromones. [4] The males use their larger antennae to detect the pheromones. After mating, the females die following egg laying. These moths have vestigial mouthparts and do not eat in the adult stage. [8] [10]

Conservation status

The Io moth has not been evaluated for listing on the IUCN Red List and has no special status on the U.S. Federal List. [19] In the eastern range of the US, the populations indicate a declining and more localized trend. [22] [19]    

Automeris io by Titian Peale, 1833 Automeris io Titian Peale 1833.jpg
Automeris io by Titian Peale, 1833

See also

Related Research Articles

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<span class="mw-page-title-main">Urticating hair</span> Bristles on plants and animals that cause physical irritation when embedded

Urticating hairs or urticating bristles are one of the primary defense mechanisms used by numerous plants, almost all New World tarantulas, and various lepidopteran caterpillars. Urtica is Latin for "nettle", and bristles that urticate are characteristic of this type of plant, and many other plants in several families. This term also refers to certain types of barbed bristles that cover the dorsal and posterior surface of a tarantula's or caterpillar's abdomen. Many tarantula species eject bristles from their abdomens, directing them toward potential attackers. These bristles can embed themselves in the other animal's skin or eyes, causing physical irritation, usually to great discomfort. The term "hairs" is technically a misnomer, as technically only mammals possess true hairs. The technical word for plant hairs is trichomes.

<span class="mw-page-title-main">Saturniidae</span> Family of moths

Saturniidae, members of which are commonly named the saturniids, is a family of Lepidoptera with an estimated 2,300 described species. The family contains some of the largest species of moths in the world. Notable members include the emperor moths, royal moths, and giant silk moths.

<i>Saturnia pavonia</i> Species of moth

Saturnia pavonia, the small emperor moth, is a moth of the family Saturniidae. It was first described by Carl Linnaeus in his 1758 10th edition of Systema Naturae. Sometimes, the incorrect genus name Pavonia is still used for this species. This moth occurs throughout the Palearctic region and is the only member of its family to be found in the British Isles, where it is usually called simply the emperor moth.

<i>Manduca quinquemaculata</i> Species of moth

Manduca quinquemaculata, the five-spotted hawkmoth, is a brown and gray hawk moth of the family Sphingidae. The caterpillar, often referred to as the tomato hornworm, can be a major pest in gardens; they get their name from a dark projection on their posterior end and their use of tomatoes as host plants. Tomato hornworms are closely related to the tobacco hornworm Manduca sexta. This confusion arises because caterpillars of both species have similar morphologies and feed on the foliage of various plants from the family Solanaceae, so either species can be found on tobacco or tomato leaves. Because of this, the plant on which the caterpillar is found does not indicate its species.

<i>Antheraea polyphemus</i> Species of moth

Antheraea polyphemus, the Polyphemus moth, is a North American member of the family Saturniidae, the giant silk moths. It is a tan-colored moth, with an average wingspan of 15 cm (6 in). The most notable feature of the moth is its large, purplish eyespots on its two hindwings. The eyespots give it its name – from the Greek myth of the cyclops Polyphemus. The species was first described by Pieter Cramer in 1776. The species is widespread in continental North America, with local populations found throughout subarctic Canada and the United States. The caterpillar can eat 86,000 times its weight at emergence in a little less than two months. Polyphemus moths are considered to be very polyphagous, meaning they eat from a wide variety of plants.

<i>Hyalophora cecropia</i> Species of moth

Hyalophora cecropia, the cecropia moth, is North America's largest native moth. It is a member of the family Saturniidae, or giant silk moths. Females have been documented with a wingspan of five to seven inches or more. These moths can be found all across North America as far west as Washington and north into the majority of Canadian provinces. Cecropia moth larvae are most commonly found on maple trees, but they have also been found on cherry and birch trees among many others. The species was first described by Carl Linnaeus in his 1758 10th edition of Systema Naturae.

<i>Dryocampa rubicunda</i> Species of moth

Dryocampa rubicunda, the rosy maple moth, is a small North American moth in the family Saturniidae, also known as the great silk moths. It was first described by Johan Christian Fabricius in 1793. The species is known for its wooly body and pink and yellow coloration, which varies from cream or white to bright pink or yellow. Males have bushier antennae than females, which allow them to sense female pheromones for mating.

<i>Citheronia regalis</i> Species of moth

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<i>Actias isis</i> Species of moth

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<i>Callosamia promethea</i> Species of moth

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<i>Anthela nicothoe</i> Species of moth

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<i>Eupackardia</i> Genus of moths

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<i>Hylesia nigricans</i> Species of moth

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<i>Cotesia glomerata</i> Species of wasp

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<i>Hemileuca lucina</i> Species of moth

Hemileuca lucina, the New England buck moth, is a species of moth in the family Saturniidae. This moth species is only found in the New England region of the United States. Larvae in early stages mainly feed on broadleaf meadowsweet whereas larvae in later stages show variation in food sources such as blackberry and black cherry leaves. Larvae have a black body with orange/black spines on their back that are used to deter predators. Pupation occurs during the summer and adult moths come out around September.

References

  1. NatureServe (May 5, 2023). "Automeris io". NatureServe Network Biodiversity Location Data accessed through NatureServe Explorer. Arlington, Virginia: NatureServe. Retrieved May 19, 2023.
  2. Fabricius, Johan Christian (1775). Systema entomologiae: sistens insectorvm classes, ordines, genera, species, adiectis synonymis, locis, descriptionibvs, observationibvs (PDF) (in Latin). Flensbvrgi et Lipsiae: In Officina Libraria Kortii. p. 560. doi:10.5962/bhl.title.36510. OCLC   559265566 . Retrieved March 15, 2018.
  3. "Automeris io (Fabricius, 1775)". Integrated Taxonomic Information System . Retrieved May 19, 2023.
  4. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 Hall, Donald W. (November 2014). "Featured Creatures: Io moth". Institute for Food and Agricultural Sciences. University of Florida. Retrieved May 19, 2023.
  5. "Species Automeris io - Io Moth - Hodges#7746". bugguide.net. Retrieved February 22, 2022.
  6. Triant, Deborah A (2016). "Genome assembly and annotation of the io moth,Automeris io (Lepidoptera: Saturniidae)". 2016 International Congress of Entomology. Entomological Society of America. doi:10.1603/ice.2016.114514.
  7. 1 2 3 4 5 "Io moth Automeris io (Fabricius, 1775) | Butterflies and Moths of North America". www.butterfliesandmoths.org. Retrieved February 16, 2022.
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  9. 1 2 Hossler, Eric; Elston, Dirk; Wagner, David (2008). "What's Eating You? Automeris io" (PDF). Cutis. 82: 21–24.
  10. 1 2 3 4 5 6 7 "Io Moth". Missouri Department of Conservation. Retrieved February 23, 2022.
  11. 1 2 3 Sourakov, Andrei (September 26, 2017). "Giving eyespots a shiner: Pharmacologic manipulation of the Io moth wing pattern". F1000Research. 6: 1319. doi: 10.12688/f1000research.12258.2 . ISSN   2046-1402. PMC   5629545 . PMID   29057069.
  12. 1 2 3 Stevens, Martin (November 2005). "The role of eyespots as anti-predator mechanisms, principally demonstrated in the Lepidoptera". Biological Reviews. 80 (4): 573–588. doi:10.1017/S1464793105006810. ISSN   1469-185X. PMID   16221330. S2CID   24868603.
  13. O’Hara, James E.; Wood, D. Monty (December 1998). "Tachinidae (Diptera): Nomenclatural Review and Changes, Primarily for America North of Mexico". The Canadian Entomologist. 130 (6): 751–774. doi:10.4039/ent130751-6. ISSN   0008-347X. S2CID   86402092.
  14. Ellis, Carter Reid; Elston, Dirk M.; Hossler, Eric W.; Cowper, Shawn E.; Rapini, Ronald P. (2021). "What's Eating You? Caterpillars" (PDF). Cutis. 108 (6): 346–351. doi:10.12788/cutis.0406. PMID   35167790. S2CID   246865715.
  15. Villas-Boas, Isadora Maria; Alvarez-Flores, Miryam Paola; Chudzinski-Tavassi, Ana Marisa; Tambourgi, Denise V. (2016). "Envenomation by Caterpillars". Clinical Toxinology in Australia, Europe, and Americas. Vol. 57. pp. 429–449. doi:10.1007/978-94-017-7438-3_57. ISBN   978-94-017-7436-9.
  16. Jones, David L.; Miller, Joseph H. (January 1, 1959). "Pathology of the Dermatitis Produced by the Urticating Caterpillar, Automeris Io". A.M.A. Archives of Dermatology. 79 (1): 81–85. doi:10.1001/archderm.1959.01560130083009. ISSN   0096-5359. PMID   13605279.
  17. Sourakov, Andrei (2013). "Larvae of Io Moth, Automeris io, On the Coral Bean, Erythrina herbacea, in Florida—the Limitations of Polyphagy". The Journal of the Lepidopterists' Society. 67 (4): 291–298. doi:10.18473/lepi.v67i4.a6. S2CID   87172312 . Retrieved February 16, 2022.
  18. Barbour, James; Kiviat, Erik (January 10, 2018). "Introduced Purple Loosestrife as Host of Native Saturniidae (Lepidoptera)". The Great Lakes Entomologist. 30 (2). doi: 10.22543/0090-0222.1934 . ISSN   0090-0222. S2CID   86194749.
  19. 1 2 3 4 Miner, Angela (2014). Martina, Leila Siciliano (ed.). "Automeris io". Animal Diversity Web. Retrieved May 20, 2023.
  20. "Species Automeris io - Io Moth - Hodges#7746". bugguide.net. Retrieved February 16, 2022.
  21. 1 2 "Adult and Larva of Moths of Pennsylvania: Moths and Butterflies" (PDF). WRCF Poster. Retrieved February 16, 2022.
  22. Wagner, David (2012). "Conservation Matters: Moth Decline in the Northeastern United States" (PDF). News of the Lepidopterists' Society. 54: 52–55.