Dryocampa rubicundarosy maple moth

Ge­o­graphic Range

Rosy maple moths are na­tive to North Amer­ica. The north­ern ex­tent of their range is in south­ern Canada, and they have been recorded in south­ern On­tario, Que­bec, New Brunswick, Nova Sco­tia and Prince Ed­ward Is­land. They range down the East Coast of the United States through most of Florida. Their range ex­tends west to Michi­gan, In­di­ana, Texas, Kansas, and Ne­braska. ("The Green Striped Maple Worm", 1971; Collins, et al., 1996; Co­ti­nis, 2004; Forbes, 1960; Hyche, 2000; Oehlke, 2005; Opler, et al., 2012; VanDyke, 2006; Ward and Her­bert, 1974)

Habi­tat

Rosy maple moths in­habit tem­per­ate de­cid­u­ous forests of east­ern North Amer­ica. They are most often as­so­ci­ated with red maples (Acer rubrum), sugar maples (Acer sac­cha­rum), sil­ver maples (Acer sac­cha­r­inum), turkey oaks (Quer­cus lae­vis) and box elder maples (Acer ne­gundo). De­pend­ing on where their host trees are, rosy maple moths have also been found in sub­ur­ban areas. ("The Green Striped Maple Worm", 1971; Co­ti­nis, 2004; Hyche, 2000; Opler, et al., 2012; VanDyke, 2006)

Phys­i­cal De­scrip­tion

Adult rosy maple moths are ex­tremely vari­able in color. Col­oration in adults can range from un­marked white to bright yel­low with dark pink mac­u­la­tion. The woolly body of rosy maple moths varies in color from bright yel­low, to cream, to white. Their ven­tral side, legs, and an­ten­nae are usu­ally rose pink. Upper wing color is also very vari­able; rang­ing from yel­low to cream, to white with pink at the mar­gins and bases of the wing. The amount of pink mac­u­la­tion on the wings ranges from dom­i­nant to nearly ab­sent. Poly­mor­phism does occur within dif­fer­ent ge­o­graphic re­gions. Unique to Mis­souri, sub­species alba is ei­ther all white or white with very faint pink mac­u­la­tion. (Collins, et al., 1996; Co­ti­nis, 2004)

Sex­ual di­mor­phism is pre­sent in wing shape and span of rosy maple moths. Males have slightly nar­rower wings com­pared to fe­males, and also have less rounded hind­wings. Or­na­men­ta­tion dif­fer­ences are also pre­sent. Males have bipecti­nate an­ten­nae, while fe­males have sim­ple an­ten­nae. Both male and fe­male rosy maple moths have an av­er­age wingspan of 32 to 55 mm. Male forewing length ranges from 17 to 29 mm. The last in­star ranges from 38 mm to 55 mm in length. (Collins, et al., 1996; Co­ti­nis, 2004; VanDyke, 2006)

Rosy maple moth cater­pil­lars, also known as green-striped maple­worms, have dif­fer­ent col­oration de­pend­ing on their stage of de­vel­op­ment. Early stage lar­vae have black heads and bod­ies that are yel­low­ish-cream with faint lon­gi­tu­di­nal green stripes. Fully-grown cater­pil­lars have beige to bright red heads. Their bod­ies are yel­low-green with seven dark green lines run­ning length­wise. The lon­gi­tu­di­nal line col­oration can also range from frosty blue to blue green, or black. Promi­nent black horns are lo­cated dor­sally on the sec­ond tho­racic seg­ment. Two rows of short spines run along each side of the body and the ter­mi­nal ab­dom­i­nal seg­ments have four larger spines. Other moths in the same fam­ily (Sat­urni­idae) have sim­i­lar horned lar­vae, but lack the stun­ning color of rosy maple moths. ("The Green Striped Maple Worm", 1971; "The Green­striped Maple­worm", 2010; Hyche, 2000)

  • Sexual Dimorphism
  • sexes alike
  • sexes shaped differently
  • ornamentation
  • Range length
    38 to 55 mm
    1.50 to 2.17 in
  • Range wingspan
    32 to 55 mm
    1.26 to 2.17 in

De­vel­op­ment

Fe­male rosy maple moths lay their fer­til­ized eggs 24 hours after mat­ing on the un­der­side of the host leaf and then de­part. After 2 weeks, the lar­vae hatch. Rosy maple moth lar­vae go through five in­star stages. Dur­ing the first three in­stars, the lar­vae live and eat to­gether. Only by the 4th in­star do the lar­vae feed in­de­pen­dently. Dur­ing the early in­stars, the lar­vae have shiny black heads and yel­low bod­ies with black dor­sal lines run­ning ver­ti­cally. The sec­ond body seg­ments of the lar­vae have two yel­low tu­ber­cles, each ter­mi­nat­ing with two setae. Their bod­ies are sparsely cov­ered with short setae. Their legs are black and have yel­low tips. As they pass through the sec­ond and third in­stars, their body color and stripes begin to darken. Be­tween 6 to 11 days after hatch­ing, the brood molts and emerges with deeper col­ors, two long black dor­sal horns near their head, and 6 short but sharp spines on the rest of the seg­ments. About 12 days after hatch­ing, the lar­vae un­dergo an­other molt. This molt leaves the lar­vae rel­a­tively the same in ap­pear­ance. About 1 week later, the lar­vae un­dergo a third molt and emerge with brown heads and var­ied body col­ors. The body col­ors range from dark and light green, black and green, and black and yel­low. Spot­ting also oc­curs in their first seg­ments. Pu­pa­tion oc­curs 10 to 14 days after the third molt. Pupae stages vary in length from 4 to 7 days. (Collins, et al., 1996; Eliot and Soule, 1902; Packard, 1893; VanDyke, 2006)

Re­pro­duc­tion

Mat­ing be­hav­iors of rosy maple moths are not well un­der­stood. Adults come out in the late af­ter­noon or early evening and mate at night. Fer­til­iza­tion is in­ter­nal. The fol­low­ing dusk, fe­males lay their fer­til­ized eggs. Fe­males lay their eggs on the un­der­side of host tree leaves, such as the leaves of the sugar maple tree (Acer sac­cha­r­inum). Rosy maple moths have a poly­gyan­drous mat­ing sys­tem where fe­males and males mate with dif­fer­ent part­ners through­out the breed­ing sea­son. For each new brood, rosy maple moth fe­males find a dif­fer­ent male. (Opler, et al., 2012; Packard, 1893; VanDyke, 2006)

Sex­u­ally ma­ture adult rosy maple moths emerge from pupae from mid-May through mid-July. Ovipo­si­tion peaks in early July. Rosy maple moths are oviparous, and fe­males lay eggs 24 hours after in­ter­nal fer­til­iza­tion by the male. Fe­males lay 150 to 200 eggs after fer­til­iza­tion and de­posit them in clus­ters of 10 to 30 on the un­der­side of the host leaf. The lar­vae hatch after 2 weeks and live and feed gre­gar­i­ously until the final in­stars. Lar­vae feed until mid-Au­gust at the lat­est. Over­win­ter pu­pa­tion can occur. If this hap­pens, the pupae bur­row into the soil and wait for more fa­vor­able con­di­tions to emerge. Rosy maple moths are sex­u­ally ma­ture at 2 to 9 months. ("The Green­striped Maple­worm", 2010; Jervis, et al., 2005; Packard, 1893; VanDyke, 2006)

Egg-lay­ing oc­curs at dif­fer­ent times in the year de­pend­ing on the re­gion in­hab­ited by the fe­males. In Canada and north­ern re­gions of the United States, fe­males lay one brood from May to Au­gust. In the south­ern states, fe­males lay two broods from April to Sep­tem­ber. In the Deep South in­clud­ing Florida, fe­males lay three broods from March to Oc­to­ber. (VanDyke, 2006)

  • Breeding interval
    Rosy maple moths breed one to three times in a season, depending on the latitude of their host tree.
  • Breeding season
    Oviposition peaks in early July, though females living farthest south breed from March to October.
  • Range eggs per season
    150 to 200
  • Average gestation period
    24 hours
  • Range time to independence
    0 to 0 days
  • Range age at sexual or reproductive maturity (female)
    2 to 9 months
  • Range age at sexual or reproductive maturity (male)
    2 to 9 months

Parental care is nearly ab­sent in rosy maple moths. Dur­ing the 24 hours after fer­til­iza­tion but be­fore the fe­male lays her eggs, she will yolk and pro­tect her eggs in­side her body. Fe­males lay their eggs on the un­der­side of the leaves of the host tree and leave. Males do noth­ing more than fer­til­ize the eggs. (Packard, 1893; VanDyke, 2006)

  • Parental Investment
  • female parental care
  • pre-fertilization
    • provisioning
    • protecting
      • female
  • pre-hatching/birth
    • provisioning
      • female
    • protecting
      • female

Lifes­pan/Longevity

Lifes­pan of rosy maple moths ranges from 2 to 9 months in the wild if over­win­ter pu­pa­tion oc­curs. Typ­i­cally, rosy maple moths raised in cap­tiv­ity have a shorter lifes­pan of around 2 to 5 months. In the wild, much of their life is spent over­win­ter­ing in the pupal stage. In cap­tiv­ity, there is no need to over­win­ter due to un­fa­vor­able con­di­tions. (Collins, et al., 1996; Eliot and Soule, 1902; Jervis, et al., 2005; VanDyke, 2006)

  • Typical lifespan
    Status: wild
    2 to 9 months
  • Typical lifespan
    Status: captivity
    1 to 3 months

Be­hav­ior

Rosy maple moths are noc­tur­nal and mainly soli­tary ex­cept dur­ing mat­ing. Adults enter a stage of tor­por dur­ing the morn­ing and af­ter­noon. They come out in the late af­ter­noon and mate in the late evening. At night, fe­males emit pheromones to at­tract males. Fe­males lay eggs at dusk the day after mat­ing. Adult rosy maple moths usu­ally fly dur­ing the first third of the night. Early rosy maple moth lar­vae feed to­gether but are not con­sid­ered to feed in colonies. The lar­vae be­come soli­tary feed­ers as they de­velop into late-stage cater­pil­lars. Fully-grown cater­pil­lars use the win­ter to pu­pate in shal­low holes un­der­ground. ("The Green Striped Maple Worm", 1971; Fullard and Napoleone, 2001; Opler, et al., 2012)

Home Range

Adult rosy maple moths in­habit a large range since they do not re­quire food, but the exact size of the range is un­known. Lar­vae and cater­pil­lars live on the same tree they hatched on. The lar­vae eat only the leaves and usu­ally stay on the un­der­side of the leaves. ("The Green Striped Maple Worm", 1971; "The Green­striped Maple­worm", 2010; Collins, et al., 1996; Co­ti­nis, 2004; Hyche, 2000; Opler, et al., 2012; Packard, 1893; VanDyke, 2006)

Com­mu­ni­ca­tion and Per­cep­tion

Sen­sory re­cep­tors of rosy maple moths are con­cen­trated in the an­ten­nae, legs and palps. Adults use re­cep­tors to smell pher­e­mones of the op­po­site sex when it is time to mate. Be­cause adult rosy maple moths do not feed, their re­cep­tors are not used for find­ing food and are con­cen­trated for re­pro­duc­tive pur­poses. Rosy maple moths are equipped with com­pound eyes and sim­ple eyes, which allow them to see ul­tra­vi­o­let rays. How­ever, the com­plex­ity of the eye changes with each de­vel­op­men­tal stage. Green-striped maple worms, their cater­pil­lars, only have sim­ple eyes that can dif­fer­en­ti­ate be­tween light and dark. Thus, their vi­sion is poor. Adults and cater­pil­lars both use their many setae to relay tac­tile in­for­ma­tion about their en­vi­ron­ment to the brain. Adults also use their body and an­ten­nae setae to sense the di­rec­tion of the wind while fly­ing. Rosy maple moths lack or­gans to process au­di­tory sounds. As cater­pil­lars and adults, rosy maple moths use their bright col­oration as a warn­ing sign and to seem dis­taste­ful to preda­tors. (Bai­ley and Horn, 2007; Collins, et al., 1996; Fullard and Napoleone, 2001)

Food Habits

Adult rosy maple moths do not feed. The trees that fe­males laid their eggs under be­come the host for the de­vel­op­ing lar­vae. The early lar­vae feed in union, how­ever, lar­vae be­come soli­tary feed­ers in the later stages. Dur­ing the molt­ing process, cater­pil­lars feed on the un­der­sides of the maple tree (Acer) or leaves of oak trees (Quer­cus). The lar­vae and cater­pil­lars are fo­liv­o­rous, and con­sume the en­tire leaf blade. ("The Green Striped Maple Worm", 1971; Opler, et al., 2012; Packard, 1893)

  • Plant Foods
  • leaves

Pre­da­tion

Rosy maple moths lay eggs on the un­der­side of leaves so as to shield them from the eyes of hun­gry birds. Green-striped maple­worms ex­hibit apose­matic col­or­ing in their black spikes and red head. They also have cryp­tic col­oration since they are a bright green; typ­i­cally the color of the leaves they live and feed on. Adult rosy maple moths ex­hibit apose­matic be­hav­ior with their bright yel­low and pink col­or­ing. Among blue­jays (Cyanocitta cristata), black-capped chick­adees (Parus atr­i­capil­lus), and tufted tit­mouses (Parus bi­color), blue­jays are the most suc­cess­ful preda­tors of rosy maple moths. Field stud­ies have shown that rosy maple moths have low ac­cept­abil­ity to birds. The main preda­tors of rosy maple moths and cater­pil­lars are the local birds. ("The Green Striped Maple Worm", 1971; "The Green­striped Maple­worm", 2010; Bai­ley and Horn, 2007; Collins, et al., 1996; Fullard and Napoleone, 2001; Sargeant, 1995)

Ecosys­tem Roles

Since adult rosy maple moths do not eat, they not im­pact the ecosys­tem as preda­tors. Lar­vae and cater­pil­lars, how­ever, can be pests when oc­cur­ring in large num­bers on the leaves of maple and oak species, in­clud­ing sugar maples (Acer sac­cha­rum), red maples (Acer rubrum), sil­ver maples (Acer sac­cha­r­inum), elder box maples (Acer ne­gundo), and oak trees (Quer­cus cer­ris). Sev­eral bird species prey on rosy maple moth lar­vae, but bird pre­da­tion is not in­tense enough to slow the pop­u­la­tion buildup. Some par­a­sites have ac­cu­mu­lated in the lar­vae, such as one species of par­a­sitic wasp (Hy­posoter fugi­tivus) and one species of fly (Achaetoneura frenchii). The par­a­sites are not abun­dant enough to af­fect the pop­u­la­tion size of the green-striped maple­worms. ("The Green Striped Maple Worm", 1971; "The Green­striped Maple­worm", 2010; Opler, et al., 2012)

Species Used as Host
  • sugar maples (Acer sac­cha­rum)
  • red maples (Acer rubrum)
  • sil­ver maples (Acer sac­cha­r­inum)
  • elder box maples (Acer ne­gundo)
  • oak trees (Quer­cus cer­ris)
Com­men­sal/Par­a­sitic Species

Eco­nomic Im­por­tance for Hu­mans: Pos­i­tive

There are no known pos­i­tive eco­nomic im­pacts of rosy maple moths on hu­mans.

Eco­nomic Im­por­tance for Hu­mans: Neg­a­tive

Adult rosy maple moths are not known to have neg­a­tive eco­nomic im­pacts on hu­mans. How­ever, lar­vae are de­fo­lia­tors ca­pa­ble of de­fo­li­at­ing their host trees dur­ing a pop­u­la­tion ex­plo­sion. If two gen­er­a­tions are pro­duced in a sin­gle year, host trees can be com­pletely stripped of leaves twice. Typ­i­cally this does not kill or per­ma­nently dam­age the tree. Nonethe­less, this can de­fo­li­ate acres of trees in a short time pe­riod if ac­com­pa­nied by an­other other hard­wood de­fo­lia­tor, sad­dled promi­nent moths (Het­e­ro­campa gut­tivitta). In ad­di­tion rosy maple moth lar­vae can be a nui­sance to dec­o­ra­tive trees as house pests. ("The Green Striped Maple Worm", 1971; "The Green­striped Maple­worm", 2010; Collins, et al., 1996; Co­ti­nis, 2004; Cov­ell, 1984; Fullard and Napoleone, 2001; Hyche, 2000; Oehlke, 2005; Opler, et al., 2012; VanDyke, 2006)

  • Negative Impacts
  • household pest

Con­ser­va­tion Sta­tus

Rosy maple moths are not con­sid­ered threat­ened or en­dan­gered. (VanDyke, 2006)

Con­trib­u­tors

Ali­cia Damele (au­thor), Uni­ver­sity of Michi­gan-Ann Arbor, Cather­ine Kent (ed­i­tor), Spe­cial Pro­jects.

Glossary

Nearctic

living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.

World Map

aposematic

having coloration that serves a protective function for the animal, usually used to refer to animals with colors that warn predators of their toxicity. For example: animals with bright red or yellow coloration are often toxic or distasteful.

arboreal

Referring to an animal that lives in trees; tree-climbing.

bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.

chemical

uses smells or other chemicals to communicate

cryptic

having markings, coloration, shapes, or other features that cause an animal to be camouflaged in its natural environment; being difficult to see or otherwise detect.

ectothermic

animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature

female parental care

parental care is carried out by females

fertilization

union of egg and spermatozoan

folivore

an animal that mainly eats leaves.

forest

forest biomes are dominated by trees, otherwise forest biomes can vary widely in amount of precipitation and seasonality.

herbivore

An animal that eats mainly plants or parts of plants.

hibernation

the state that some animals enter during winter in which normal physiological processes are significantly reduced, thus lowering the animal's energy requirements. The act or condition of passing winter in a torpid or resting state, typically involving the abandonment of homoiothermy in mammals.

internal fertilization

fertilization takes place within the female's body

metamorphosis

A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.

motile

having the capacity to move from one place to another.

native range

the area in which the animal is naturally found, the region in which it is endemic.

nocturnal

active during the night

oviparous

reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.

pheromones

chemicals released into air or water that are detected by and responded to by other animals of the same species

polygynandrous

the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.

polymorphic

"many forms." A species is polymorphic if its individuals can be divided into two or more easily recognized groups, based on structure, color, or other similar characteristics. The term only applies when the distinct groups can be found in the same area; graded or clinal variation throughout the range of a species (e.g. a north-to-south decrease in size) is not polymorphism. Polymorphic characteristics may be inherited because the differences have a genetic basis, or they may be the result of environmental influences. We do not consider sexual differences (i.e. sexual dimorphism), seasonal changes (e.g. change in fur color), or age-related changes to be polymorphic. Polymorphism in a local population can be an adaptation to prevent density-dependent predation, where predators preferentially prey on the most common morph.

seasonal breeding

breeding is confined to a particular season

sexual

reproduction that includes combining the genetic contribution of two individuals, a male and a female

sexual ornamentation

one of the sexes (usually males) has special physical structures used in courting the other sex or fighting the same sex. For example: antlers, elongated tails, special spurs.

solitary

lives alone

suburban

living in residential areas on the outskirts of large cities or towns.

tactile

uses touch to communicate

temperate

that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).

visual

uses sight to communicate

Ref­er­ences

U.S. De­part­ment of Agri­cul­ture and For­est Ser­vices. The Green Striped Maple Worm. Leaflet 77. St. Paul, Min­nesota: U.S. Gov­ern­ment Print­ing Of­fice. 1971. Ac­cessed Feb­ru­ary 24, 2012 at http://​na.​fs.​fed.​us/​spfo/​pubs/​fidls/​gs_​mapleworm/​gsm.​htm.

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Bal­lard, J. 1890. Among the Moths and But­ter­flies. New York: G.P Put­nam and Sons.

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Packard, A. 1893. The Life His­to­ries of Cer­tain Moths of the Fam­i­lies Cer­a­to­campidœ, Hemileu­cidœ, etc., with Notes on the Ar­ma­ture of the Larvœ. Pro­ceed­ings of the Amer­i­can Philo­soph­i­cal So­ci­ety, 31/141: 139-192.

Ri­otte, J. 1992. Mis­cel­la­neous Pub­li­ca­tions in the Life Sci­ences. Toronto, Canada: Royal On­tario Mu­seum.

Roeder, K. 1974. Acoustic sen­sory re­sponses and pos­si­ble bat- eva­sion tac­tics of cer­tain moths. Pro­ceed­ings of the Cana­dian So­ci­ety of Zo­ol­o­gists An­nual Meet­ing: 71-78.

Sargeant, T. 1995. On the Rel­a­tive Ac­cept­abil­i­ties of Local But­ter­flies and Moths to Local Birds. Jour­nal of the Lep­i­dopter­ists' So­ci­ety, 49(2): 148-162. Ac­cessed March 26, 2012 at http://​peabody.​research.​yale.​edu/​jls/​pdfs/​1990s/​1995/​1995-49(2)148-Sargent.​pdf.

VanDyke, J. 2006. ""Dry­ocam­pus ru­bi­cunda"" (On-line). Ac­cessed Feb­ru­ary 02, 2012 at <http://​bugguide.​net/​node/​view/​15740>..

Ward, H., P. Her­bert. 1974. The Macro­hete- ro­cera of south-east­ern On­tario. Jour­nal of Re­search on the Lep­i­doptera, 13: 23-42.