Brown-tail moth

Last updated

Euproctis chrysorrhoea
Euproctis chrysorrhoea 1.jpg
Upperside
Euproctis chrysorrhoea (Linnaeus, 1758).jpg
Female with tail tuft of red/brown hairs
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Superfamily: Noctuoidea
Family: Erebidae
Genus: Euproctis
Species:
E. chrysorrhoea
Binomial name
Euproctis chrysorrhoea

The brown-tail moth (Euproctis chrysorrhoea) is a moth of the family Erebidae. It is native to Europe, neighboring countries in Asia, and the north coast of Africa. Descriptions of outbreaks, i.e., large population increases of several years duration, have been reported as far back as the 1500s. [1] The life cycle of the moth is atypical, in that it spends approximately nine months (August to April) as larvae (caterpillars), leaving about one month each for pupae, imagos and eggs. Larvae (caterpillars) are covered in hairs. Two red spots on the back, toward the tail, distinguish these species from other similarly hairy moth larvae. The winged adults have white wings and a hairy white body with a tuft of brown hair at the tip of the abdomen. Females lay one egg cluster, usually on the underside of a leaf of a host plant. The species is polyphagous, meaning that it feeds on many different species of trees, including pear, apple, maple and oak.

Contents

This species was accidentally introduced to the United States in the 1890s. [1] During the early 20th century it was present from eastern Connecticut northward into New Brunswick, Canada, but a subsequent severe population collapse reduced the territory to parts of coastal Maine and Cape Cod, Massachusetts, by the late 20th century. One theory for the decline appeared to be parasitism by a fly introduced to combat spongy moths. [2] Starting in 2015 there has been a population spike and territory expansion in coastal Maine. [3] In Europe, there are multiple parasitic and predator species, [4] yet there is still a history of population outbreaks.

Hairs from the caterpillars are toxic for humans, [5] causing a poison ivy-like itchy rash of up to sometimes weeks-long duration due to mechanical and chemical irritation. [6] [7] Direct contact with larvae is not necessary, as the hairs are shed and can become windblown. [5] Toxins in the hairs remain potent for up to three years. Outdoor activities such as mowing a lawn or raking leaves in the fall can cause exposure. [5]

Description

Caterpillar, dorsal view, showing two red dots near tail Lymantriidae - Euproctis chrysorrhoea.JPG
Caterpillar, dorsal view, showing two red dots near tail

The upper surface of the wings of this species is pure white. Males may have some brown color on the underside of the forewing. Wingspan is 36–42 millimetres (1.4–1.7 in). The body is very hairy and white except for the tail which is covered in reddish-brown hairs, much more prominent in the females. [8] Males have larger antennae, used to detect pheromones released by unmated females. Females have a larger body. [8] As winged adults, this species is superficially similar in appearance to Euproctis similis (native to Europe) and Hyphantria cunea (native to North America), but female E. similis have a yellow tail tuft and H. cunea lacks tail tuft coloration.

The female lays one cluster of 200 to 400 eggs, typically on the underside of a leaf. The egg cluster is covered with hairs from her anal tuft. [8] The larva is very hairy, brown with white markings, and two prominent red spots toward the tail end. The hairs provide protection from predators; the larva incorporates some into the cocoon within which it pupates. [9] The species overwinters communally as larvae within a tough, silken tent constructed around branch-tip leaves and anchored to twigs. In areas where the species is abundant, these tents are a familiar sight, and can be seen on a huge range of plants, especially in late fall and winter when unaffected leaves have fallen. [3] [5]

Distribution

Native

This species can be found throughout Europe, except in the most northern countries, also in the westernmost countries of Asia, such as Turkey, Syria and Israel, and the countries across the northern parts of Africa. [10] Charles H. Fernald and Archie H. Kirkland recount historic mentions of brown-tail moths dating back to 1500s, describing outbreaks in Paris, London and Berlin so severe as to completely strip all trees of leaves. Carl Linnaeus described the species in the tenth edition (1758) of Systema Naturae . [1]

Invasive

The brown-tail moth is an invasive species in the United States and Canada, having arrived in Somerville, Massachusetts, circa 1890 and becoming widespread there and in neighboring Cambridge by 1897. Initial outbreaks were most evident in pear and apple trees. Doctors reported "poisonings" (skin rash) far worse than poison ivy rash. Within a few years it was seen as a serious, fast-spreading, horticultural and health problem. [1] Through the early parts of the 20th century it was present in much of New England from eastern Connecticut to Maine, and northward into New Brunswick, Canada, but the 1906 introduction of the parasitic tachinid fly Compsilura concinnata to counter spongy moths collaterally impacted brown-tail moths. By the late 20th century the habitat was reduced to the coast and islands of Maine, and also parts of Cape Cod, Massachusetts. [2] Cold and wet weather hinders re-expansion of the population outside its current territories, [11] although starting in 2015 there has been a population spike and territory expansion in coastal Maine, from Portland to Bar Harbor. [3] In addition to North America, there have been reports of this species appearing in China, Japan and New Guinea. [10]

Detection

Photographs taken from aerial fly-overs are used to identify areas where the trees have been denuded of leaves and where the branch-tip tents are present. [3] The female sex hormone has been synthesized and field-tested in moth traps as a means of monitoring moth populations during the June/July flight season. [12] The white-winged adults are nocturnal and strongly attracted to light; a report from 1903 likened their appearance around streetlights as being akin to heavy snowfall. [1]

Life cycle

The brown-tail moth produces one generation a year. It has four life stages; egg, larval, pupal, and adult. Eggs are laid in July and hatch in August. [8] The annual cycle is approximately one month as eggs, nine months as larvae, one month as pupae, and one month as imagoes (winged, sexually mature adults). [13]

  1. Eggs are preferentially laid on oak trees.
  2. Pre-diapausing larvae: Emerge and feed gregariously starting in August after about three weeks of egg incubation.
  3. Diapausing larvae: As a response to shortened periods of daylight, larvae build communal winter nests in the fall, inside of which they overwinter. These involve webbing binding leaves together at tree-top branch tips. Distinct from other communal moth larvae such as eastern tent caterpillar which over-winter as eggs, then create webbed nests in branch crotches during spring and summer.
  4. Post-diapausing gregarious larvae: The emerging larvae, approximately one centimeter long, resume feeding in early April synchronized with bud break, and still inhabit the winter nests as their resting places, or else make communal web-nests. These small larvae will also detach from trees and fall to the ground, then search for new trees.
  5. Post-diapausing dispersive larvae: Once larvae reach late instars, colonies break up and larvae start feeding independently.
  6. Pupation: Larvae pupate in June after six to eight instars.
  7. Emergence: Imagoes (winged, sexually mature adults) appear about one month later; mate, lay eggs and die. [13]

Predators, parasites and diseases

In the United States, many species of birds prey on the winged adults, including English house sparrow and blue jay. [1] A review of mortality causes in England and mainland Europe described the brown-tail moth as undergoing periodic population outbreaks, each developing rapidly and lasting for several years, followed by a decline to relative obscurity. In a study conducted in England, egg, larvae and pupae deaths were attributed to several parasites, including microsporidia, cytoplasmic and nuclear viruses, and larvae predation by birds, specifically identifying the common cuckoo (Cuculus canorus) and titmice. [14] A more recent review, conducted in Spain, identified 17 species of parasites, viral diseases, unspecified predation and other, unknown, causes of death spanning from eggs not hatching, during summer, winter and spring as larvae, finishing with pupae failing to produce winged adults. Generally, mortality increased with population density, although in outbreak regions there was some compensation by females laying 21.6% more eggs (cause not discussed). [4]

Compsilura concinnata , a parasitic fly, pierces the brown-tail moth larva and deposits its own larva inside. This fly was introduced to North America in 1906 in an attempt to counter spongy moth, an invasive species. While not entirely successful for that purpose, one research group concluded that introduction of this fly had a great impact on brown-tail moths while not being as effective on spongy moths, the reason being that the fly larvae need to over-winter inside a host larvae. (Brown-tail moths over-winter as larvae, whereas spongy moths over-winter as eggs.) [2] An older review describes other fly species that were confirmed as brown-tail moth larvae parasites, then released in U.S.: Apanteles lacteicolor, Metrous versicolor and Sturmia nidicola. [15]

Control

Branch-tip webs can be clipped in winter and very early spring, and either dropped into a bucket of soapy water or burned. Gloves should be worn. Appropriate pesticides should be applied before early May because that is when the larvae start to develop harmful hairs. For organic garden and farm situations there are sprays that use a strain of Bacillus thuringiensis (Bt). [5]

Health issues

Skin rash caused by the exposure to hairs shed by brown-tail moth larva Euproctis Chrysorrhoea skin rash cutted.png
Skin rash caused by the exposure to hairs shed by brown-tail moth larva

Cicely Blair wrote a paper about the rash caused by the brown-tail moth caterpillar in the British Isles. [16] It, and other descriptions, confirmed that loose hairs can break off and cause very itchy rashes on contact with skin, as well as breathing difficulties similar to asthma if inhaled. Rashes can persist for weeks. [6] [7] [17] [18] The same symptoms have been reported as far back as 1903. [1] The reactions are due to a combination of mechanical and chemical stimuli, the barbed hairs in effect becoming lodged in and physically irritating the skin, and also functioning as microtubules to introduce irritating chemical compounds that have hydrolase, esterase and hemolytic activity. [6] [7] This rash reaction may be referred to as lepidopterism. The species should be handled using protective gloves at all stages of its life cycle. Shed hairs blow about, and can be brought indoors on clothing and shoes, so rashes can occur without the victim coming in direct contact with the caterpillars. The toxins in the hairs remain potent for up to three years after being shed. Outdoor activities such as mowing a lawn or raking leaves in the fall can cause exposure. [3] [5]

A related species, mistletoe browntail moth ( Euproctis edwardsi ), has been reported as causing a similar rash in Australia, in people working at or visiting a community center, attributed to caterpillars feeding on a tree outside the building. [19] In addition to brown-tail and mistletoe browntail, several other Euproctis species are identified as causing rashes in humans, including Euproctis baliolalis , Euproctis limbalis and Euproctis lutea (all three native to Australia). Urticating hairs, i.e., itch and rash-producing, are also reported for caterpillars of other moth and butterfly species.

Host plants

Brown-tail larvae have been reported as feeding on 26 genera of non-resinous trees and shrubs belonging to 13 different families. This polyphagy is considered unusual. Non-specific host plant feeding combined with its tendency to reach extreme outbreak densities makes this species a major pest of fruit orchards, ornamental trees and hardwood forests. [13] Partial list of plant species: apple, cherry, beach plum (Cape Cod, Massachusetts), beech, elm, grape, hops, maple, oak, pear, raspberry, rose and willow, and even conifers like spruce and hemlock. An early description of the introduction to the United States in the 1890s identified pear and apple trees as most greatly afflicted, but mentioned that once trees were entirely bare of leaves, the larvae would descend to the ground in great numbers and move toward any leafy plant, including vegetable plants. [1] A population explosion on Orford Ness, Suffolk, Uk in 2023-2024 has denuded wild bramble/blackberry bushes.[ citation needed ]

Related Research Articles

<span class="mw-page-title-main">Lepidoptera</span> Order of insects including moths and butterflies

Lepidoptera or lepidopterans is an order of winged insects which includes butterflies and moths. About 180,000 species of the Lepidoptera have been described, representing 10% of the total described species of living organisms, making it the second largest insect order with 126 families and 46 superfamilies, and one of the most widespread and widely recognizable insect orders in the world.

<span class="mw-page-title-main">Pupa</span> Life stage of some insects undergoing transformation

A pupa is the life stage of some insects undergoing transformation between immature and mature stages. Insects that go through a pupal stage are holometabolous: they go through four distinct stages in their life cycle, the stages thereof being egg, larva, pupa, and imago. The processes of entering and completing the pupal stage are controlled by the insect's hormones, especially juvenile hormone, prothoracicotropic hormone, and ecdysone. The act of becoming a pupa is called pupation, and the act of emerging from the pupal case is called eclosion or emergence.

<span class="mw-page-title-main">Luna moth</span> Species of insect

The luna moth, also called the American moon moth, is a Nearctic moth in the family Saturniidae, subfamily Saturniinae, a group commonly named the giant silk moths.

<span class="mw-page-title-main">Winter moth</span> Species of moth

The winter moth is a moth of the family Geometridae. It is an abundant species in Europe and the Near East and a famous study organism for evaluating insect population dynamics. It is one of very few lepidopterans of temperate regions in which adults are active in late autumn and early winter. The adults use endothermy for movement in these cold temperatures. The females of this species are virtually wingless and cannot fly, but the males are fully winged and fly strongly. After the initial frosts of late fall, the females emerge from their pupae, walk to and up trees and emit pheromones in the evening to attract males. After fertilization, they ascend to lay, on average, around 100 eggs each. Typically, the larger the female moth is, the more eggs she lays.

<span class="mw-page-title-main">Pine processionary</span> Species of moth

The pine processionary is a moth of the subfamily Thaumetopoeinae in the family Notodontidae, known for the irritating hairs of its caterpillars, their processions, and the economic damage they cause in coniferous forests. The species was first described scientifically by Michael Denis and Ignaz Schiffermüller in 1775, though it was known to the ancients, with remedies described by Theophrastus, Dioscorides and Pliny the Elder. Its processionary behaviour was described in 1916 by the French entomologist Jean-Henri Fabre. It is one of the most destructive species to pines and cedars in Central Asia, North Africa and southern Europe.

<span class="mw-page-title-main">Lymantriinae</span> Subfamily of moths

The Lymantriinae are a subfamily of moths of the family Erebidae. The taxon was erected by George Hampson in 1893.

<span class="mw-page-title-main">Yellow-tail</span> Species of moth

The yellow-tail, goldtail moth or swan moth is a moth of the family Erebidae. The species was first described by Johann Kaspar Füssli in 1775, and has commonly been placed within the related genus Euproctis. It is distributed throughout Europe to the Urals, then east across the Palearctic to Siberia and south to India and Sri Lanka.

<span class="mw-page-title-main">Oak processionary</span> Species of moth

The oak processionary (OPM) is a moth whose caterpillars can be found in oak forests, where they feed on oak leaves, causing significant damage. They travel in nose-to-tail processions, often arrow-headed, with a leader followed by rows of several caterpillars abreast. They are a human irritant because of their venomous setae, which can cause skin irritation and asthma. The species was first described by Carl Linnaeus in his 1758 10th edition of Systema Naturae.

<span class="mw-page-title-main">Forest tent caterpillar moth</span> Species of insect

The forest tent caterpillar moth is a moth found throughout North America, especially in the eastern regions. Unlike related tent caterpillar species, the larvae of forest tent caterpillars do not make tents, but rather, weave a silky sheet where they lie together during molting. They also lay down strands of silk as they move over branches and travel as groups along these pheromone-containing silk trails. The caterpillars are social, traveling together to feed and massing as a group at rest. Group behavior diminishes as the caterpillars increase in size, so that by the fifth instar (molt) the caterpillars are feeding and resting independently.

<span class="mw-page-title-main">Codling moth</span> Species of moth that feeds on fruit (Cydia pomonella)

The codling moth is a member of the Lepidopteran family Tortricidae. They are major pests to agricultural crops, mainly fruits such as apples and pears, and a codling moth larva is often called an "apple worm". Because the larvae are not able to feed on leaves, they are highly dependent on fruits as a food source and thus have a significant impact on crops. The caterpillars bore into fruit and stop it from growing, which leads to premature ripening. Various means of control, including chemical, biological, and preventive, have been implemented. This moth has a widespread distribution, being found on six continents. Adaptive behavior such as diapause and multiple generations per breeding season have allowed this moth to persist even during years of bad climatic conditions.

<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>Polygonia interrogationis</i> Species of butterfly

Polygonia interrogationis, commonly called the question mark butterfly, is a North American nymphalid butterfly. It lives in wooded areas, city parks, generally in areas with a combination of trees and open space. The color and textured appearance of the underside of its wings combine to provide camouflage that resembles a dead leaf. The adult butterfly has a wingspan of 4.5–7.6 cm (1.8–3.0 in). Its flight period is from May to September. "The silver mark on the underside of the hindwing is broken into two parts, a curved line and a dot, creating a ?-shaped mark that gives the species its common name."

<i>Orgyia leucostigma</i> Species of moth

Orgyia leucostigma, the white-marked tussock moth, is a moth in the family Erebidae. The species was first described by James Edward Smith in 1797. The caterpillar is very common especially in late summer in eastern North America, extending as far west as Texas, California, and Alberta.

<i>Choristoneura fumiferana</i> Species of moth

Choristoneura fumiferana, the eastern spruce budworm, is a species of moth of the family Tortricidae native to the eastern United States and Canada. The caterpillars feed on the needles of spruce and fir trees. Eastern spruce budworm populations can experience significant oscillations, with large outbreaks sometimes resulting in wide scale tree mortality. The first recorded outbreaks of the spruce budworm in the United States occurred in about 1807, and since 1909 there have been waves of budworm outbreaks throughout the eastern United States and Canada. In Canada, the major outbreaks occurred in periods circa 1910–20, c. 1940–50, and c. 1970–80, each of which impacted millions of hectares of forest. Longer-term tree-ring studies suggest that spruce budworm outbreaks have been recurring approximately every three decades since the 16th century, and paleoecological studies suggest the spruce budworm has been breaking out in eastern North America for thousands of years.

<i>Malacosoma californicum</i> Species of insect

Malacosoma californicum, the western tent caterpillar, is a moth of the family Lasiocampidae. It is a tent caterpillar. The Western Tent Caterpillar is found in southern Canada, the western United States, and parts of northern Mexico. There are currently six recognized subspecies of M. californicum. Western tent caterpillars are gregarious and will spend a large portion of their time with other caterpillars in silken tents constructed during their larval stage.

<i>Ochrogaster lunifer</i> Species of moth

Ochrogaster lunifer, the bag-shelter moth or processionary caterpillar, is a member of the family Notodontidae. The species was first described by Gottlieb August Wilhelm Herrich-Schäffer in 1855. Both the larval and adult forms have hairs that cause irritation of the skin (urticaria). The adult moth has a woolly appearance and its wings can grow to be about 5.5 cm across. The larvae feed on Grevillea striata at night and reside in brown silken bag nest during the day.

<i>Operophtera bruceata</i> Species of moth

Operophtera bruceata, the Bruce spanworm, hunter's moth, or native winter moth is a moth of the family Geometridae. The species was first described by George Duryea Hulst in 1886. It is found from coast to coast in southern Canada and the northern parts of the United States.

<i>Lymantria dispar</i> in the United States Spread of an invasive species

The spongy moth, formerly known as the gypsy moth, was introduced in 1868 into the United States by Étienne Léopold Trouvelot, a French scientist living in Medford, Massachusetts. Because native silk-spinning caterpillars were susceptible to disease, Trouvelot imported the species in order to breed a more resistant hybrid species. Some of the moths escaped, found suitable habitat, and began breeding. The gypsy moth is now a major pest of hardwood trees in the Eastern United States.

<i>Lymantria dispar asiatica</i> Subspecies of moth

Lymantria dispar asiatica, the LDA moth or Asian spongy moth, also known as the Asian gypsy moth, is a moth in the family Erebidae of Eurasian origin. It is similar to Lymantria dispar dispar in appearance, but adult females can fly. It is classified as a pest and is host to over 500 species of trees, shrubs and plants.

<i>Lymantria dispar dispar</i> Subspecies of moth (gypsy moth)

Lymantria dispar dispar, commonly known as the gypsy moth, European gypsy moth, LDD moth, or North American gypsy moth or spongy moth, is a species of moth in the family Erebidae. It has a native range that extends over Europe and parts of Africa, and is an invasive species in North America.

References

  1. 1 2 3 4 5 6 7 8 Fernald, Charles H. & Kirkland, Archie H. (1903). "The brown-tail moth, Euproctis chrysorrhoea (L.). A report on the life history and habits of the imported brown-tail moth, together with a description of the remedies best suited for destroying it". Wright & Potter Printing Co., Boston.
  2. 1 2 3 Elkinton, J. S., Parry, D., Boettner, G. H. (2006). "Implicating an introduced generalist parasitoid in the invasive browntail moth's enigmatic demise". Ecology. 87 (10): 2664–2672. doi:10.1890/0012-9658(2006)87[2664:iaigpi]2.0.co;2. PMID   17089674.
  3. 1 2 3 4 5 "Browntail Moth History, Background, Conditions in ME" (PDF). Department of Agriculture, Conservation & Forestry, Maine Forest Service. February 2018. Retrieved 25 July 2018.
  4. 1 2 Frago E, Pujade-Villar J, Guara M, Selfa J (2011). "Providing insights into browntail moth local outbreaks by combining life table data and semi-parametric statistics". Ecological Entomology. 36 (2): 188–199. Bibcode:2011EcoEn..36..188F. doi:10.1111/j.1365-2311.2010.01259.x. S2CID   83507161.
  5. 1 2 3 4 5 6 "Browntail Moth" (PDF). Maine Department of Agriculture, Conservation and Forestry. Retrieved 24 July 2018.
  6. 1 2 3 de Jong, M. C., Hoedemaeker, J., Jongebloed, W. L., Nater, J. P. (1976). "Investigative studies of the dermatitis caused by the larva of the brown-tail moth (Euproctis chrysorrhoea Linn.) II. Histopathology of skin lesions and scanning electron microscopy of their causative setae". Archives of Dermatological Research. 255 (2): 177–191. doi:10.1007/bf00558526. PMID   1275552. S2CID   22982885.
  7. 1 2 3 de Jong, M. C., Kawamoto, F., Bleumink, E., Kloosterhuis, A. J., Meijer, G. T. (1982). "A comparative study of the spicule venom of Euproctis caterpillars". Toxicon. 20 (2): 477–485. doi:10.1016/0041-0101(82)90011-3. PMID   7043788.
  8. 1 2 3 4 "Controlling Browntail moths as they lay eggs". Harpswell Heritage Land Trust, Harpswell, Maine. 2 August 2016. Retrieved 10 July 2018.
  9. Candan S, Suludere Z, Bayrakdar F (2007). "Surface morphology of eggs of Euproctis chrysorrhoea (Linnaeus, 1758)". Acta Zoologica. 89 (2): 133–136. doi:10.1111/j.1463-6395.2007.00300.x.
  10. 1 2 "Euproctis chrysorrhoea (brown-tail moth)". CABI Invasive Species Compendium. Wallingford, UK: CAB International. 2018. Retrieved 23 July 2018.
  11. Elkinton, J. S., Preisser, E., Boettner, G., Parry, D. (2008). "Factors influencing larval survival of the invasive browntail moth (Lepidoptera: Lymantriidae) in relict North American populations". Environmental Entomology. 37 (6): 1429–1437. doi: 10.1603/0046-225x-37.6.1429 . PMID   19161686. S2CID   11928538.
  12. Khrimian, A., Lance, D. R., Schwarz, M., Leonhardt, B. A., Mastro, V. C. (2008). "Sex pheromone of browntail moth, Euproctis chrysorrhoea (L.): synthesis and field deployment". Journal of Agricultural and Food Chemistry. 56 (7): 2452–2456. doi:10.1021/jf073161w. PMID   18333615.
  13. 1 2 3 Frago E, Guara MJ, Pujade-Villar J, Selfa S (2010). "Winter feeding leads to a shifted phenology in the browntail moth Euproctis chrysorrhoea on the evergreen strawberry tree Arbutus unedo". Agricultural and Forest Entomology. 12 (4): 381–388. doi:10.1111/j.1461-9563.2010.00489.x. S2CID   85141544.
  14. Sterling PH, Speight MR (1989). "Comparative mortalities of the brown-tail moth, Euproctis chrysorrhoea (L.) (Lepidoptera: Lymantriidae), in south-east England". Botanical Journal of the Linnean Society. 101: 69–78. doi:10.1111/j.1095-8339.1989.tb00137.x.
  15. Burgess AF (1929). "Imported insect enemies of the gypsy moth and the brown-tail moth" (PDF). U.S. Department of Agriculture, Washington, DC. Retrieved 23 July 2018.
  16. Blair CP (1979). "The browntail moth, its caterpillar and their rash". Clinical and Experimental Dermatology. 4 (2): 215–222. doi:10.1111/j.1365-2230.1979.tb01621.x. PMID   498574. S2CID   31576760.
  17. Mabey, Richard, Marren, Peter (2010). Bugs Britannica (Illustrated ed.). Random House UK. p. 273. ISBN   9780701181802 . Retrieved 7 January 2016.
  18. Graham G (23 July 2015). "Got an itchy rash? Browntail moths out in force in Maine, spreading noxious hairs". Portland Press Herald. Retrieved 26 May 2016.
  19. Balit, C. R., Ptolemy, H. C., Geary, M. J., Russell, R. C., Isbister, G. K. (2001). "Outbreak of caterpillar dermatitis caused by airborne hairs of the mistletoe browntail moth (Euproctis edwardsi)". Medical Journal of Australia. 175 (11–12): 641–643. doi:10.5694/j.1326-5377.2001.tb143760.x. PMID   11837874. S2CID   26910462.