Monarch butterfly

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This article is about the species Danaus plexippus. For monarch migration, see Monarch butterfly migration.
Monarch butterfly
Monarch In May.jpg
Female
Monarch Butterfly Danaus plexippus Male 2664px.jpg
Male
Conservation status
Not evaluated (IUCN 3.1)
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Family: Nymphalidae
Tribe: Danaini
Genus: Danaus
Kluk, 1802
Species: D. plexippus
Binomial name
Danaus plexippus
(Linnaeus, 1758)
MonarchDistribution2-3a.png
Synonyms
  • Papilio plexippus Linnaeus, 1758
  • Danaus archippus (Fabricius, 1793)[1]
  • Danaus menippe (Hübner, 1816)[2]
  • Anosia plexippus Dyar, 1903

The monarch butterfly (Danaus plexippus) is a milkweed butterfly (subfamily Danainae) in the family Nymphalidae. It may be the most familiar North American butterfly. Its wings feature an easily recognizable orange and black pattern, with a wingspan of 8.9–10.2 cm (3½–4 in)[3] (the viceroy butterfly is similar in color and pattern, but is markedly smaller, and has an extra black stripe across the hind wing).

The eastern North American monarch population is notable for its multigenerational southward late summer/autumn migration from the United States and southern Canada to Mexico, covering thousands of miles. The western North American population of monarchs west of the Rocky Mountains most often migrate to sites in California but have been found in overwintering Mexico sites.[4][5] Monarchs were transported to the international space station and were bred there.[6]

Description[edit]

The monarch’s wingspan ranges from 8.9–10.2 cm (3½–4 in).[3] The upper side of the wings is tawny-orange, the veins and margins are black, and in the margins are two series of small white spots. The fore wings also have a few orange spots near the tip. The underside is similar, but the tip of the fore wing and hind wing are yellow-brown instead of tawny-orange and the white spots are larger.[7] The shape and color of the wings change at the beginning of the migration and appear redder and more elongated than later migrants.[8] wings size and shape differ between migratory and non-migratory monarchs. Monarchs from the eastern population of North America have larger and more angular forewings than those in the western population.[6]

Its flight has been described as "slow and sailing".[9]

Adults exhibit sexual dimorphism. The male has a black patch or spot of androconial scales on either hind wing (in some butterflies, these patches disperse pheromones, but are not known to do so in monarchs), and the black veins on its wing are lighter and narrower than the female’s.[10] The male is also slightly larger.[6][7] One variation has been observed in Australia, New Zealand, Indonesia and the United States termed nivosus by lepidopterists. It is grayish-white in all areas of the wings that are normally orange and is only about 1% or less of all monarchs, but populations as high as 10% exist on Oahu in Hawaii.[11]

Like all insects, the monarch has six legs, but uses the four hindlegs as it carries its two front legs against its body.[12]

Range[edit]

The range of the western and eastern populations of the monarch butterfly expands and contracts dependent upon the season. The range differs between breeding areas, migration routes and winter roosts.[6]:(p18)

In North America, the monarch ranges from southern Canada to northern South America. It has also been found in Bermuda, Cook Islands,[13] Hawaii, Cuba[14] and other Caribbean islands[6]:(p18) the Solomons, New Caledonia, New Zealand,[15] Papua New Guinea,[16] Australia, New Guinea, Sri Lanka, India, Nepal, the Azores, the Canary Islands Philippines, North Africa[17] and Honolulu.[18][19] It appears in the UK in some years as an acccidental.[20] No genetic differences between monarch populations exist.[21] Reproductive isolation has had no effect in creating sub species.[6]:(p19)

Status[edit]

The monarch butterfly is not currently listed under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) or protected specifically under U.S. domestic laws.[22] On 14 August 2014, the Center for Biological Diversity and the Center for Food Safety filed a legal petition requesting Endangered Species Act protection for the monarch and its habitat.[6]

Habitat[edit]

Overwintering populations of D. plexippus are found in Mexico, California, along the Gulf coast, year-round in Florida, and in Arizona where the habitat provides the specific conditions necessary for their survival.[23][24] The overwintering habitat typically provides access to streams, plenty of sunlight (for body temperatures that allow flight), appropriate vegetation on which to roost, and is relatively free of predators. Overwintering, roosting butterflies have been seen on sumacs, locusts, basswood elm, oak, osage orange, mulberry, pecan, willow, cottonwood, and mesquite.[25] While breeding, its habitat can be found in agricultural fields, pasture land, prairie remnants, urban and suburban residential areas, gardens, trees, and roadsides – anywhere where there is access to larval host plants.[26] Habitat restoration is a primary goal in monarch conservation efforts. Habitat requirements change during migration. During the fall migration, butterflies must have access to nectar-producing plants. During the spring migration, butterflies must have access to larval food plants and nectar plants.

Life cycle[edit]

The monarch undergoes the four stages of complete metamorphosis:

Eggs[edit]

Eggs are laid singly on the underside of a young leaf of a milkweed plant during the spring and summer months.[27] The eggs are cream-colored or light green, ovate to conical in shape, and about 1.2 x 0.9 mm in size. The eggs weigh less than 0.5 mg each and have raised ridges that form longitudinally from the point to apex to the base. Females lay their eggs on milkweed that make their offspring less sick.[28][29] Eggs take 3 to 8 days to develop and hatch into larva or caterpillars.[6]:(p21)

Larvae[edit]

The caterpillar goes through five major, distinct stages of growth and after each one it molts. Each caterpillar, or instar, that molts is larger than the previous as they eat and store energy in the form of fat and nutrients to carry them through the nonfeeding pupal stage.

5th instar with the white spots visible on the prolegs.

The first instar caterpillar that emerges out of the egg is pale green and translucent. It lacks banding coloration or tentacles. The larvae or caterpillar eats its egg case and begins to feed on milkweed. It is during this stage of growth that the caterpillar begins to sequester cardenolides. The caterpillar uses a circular motion while eating milkweed which prevents the flow of latex that could entrap it.

The second instar larva develops a characteristic pattern of white, yellow and black transverse bands. It is no longer translucent but is covered in short setae. Pairs of black tentacles begin to grow. One pair grows on the thorax and another pair on the abdomen.

The third instar larva has more distinct bands and the two pairs of tentacles become longer. Legs on the thorax differentiate into a smaller pair near the head and larger pairs further back. These third stage caterpillars began to eat along the leaf edges.

The fourth instar has a different banding pattern. It develops white spots on the prolegs near the back of the caterpillar.

The fifth instar larva has a more complex banding pattern and white dots on the prolegs, with front legs that are small and very close to the head.

At this stage of development is relatively large compared to the earlier instars. The caterpillar completes its growth. At this point, it is 25 to 45 mm long and 5 to 8 mm wide. This can be compared to the first instar which was 2 to 6 mm long and 0.5 to 1.5 mm wide. Fifth instar larvae increase 2000 times from first instars. Fifth stage instar larva chew through the petiole or mid-rev of milkweed leaves and stop the flow of latex. After this, they eat more leaf tissue. Before pupation, larva must consume milkweed to increase their mass prior to pupation. Larva stop feeding and search for a pupation site. The caterpillar attaches itself securely to a horizontal surface with a silk pad. At this point, it latches on with its hind legs and hangs down. It then molts into an opaque, blue-green chrysalis small with gold dots. At normal summer temperatures, it matures in a few weeks. The cuticle of the chrysalis becomes transparent and the monarchs characteristic orange and black wings become visible. At the end of metamorphosis, the adult emerges from the chrysalis, expand its wings and flies away. Monarch metamorphosis from egg to adult occurs in as little as 25 days during the warm summer temperatures come to as many as seven weeks during cool spring conditions. During the development both larva and their milkweed hosts are vulnerable to weather extremes predators, parasites and diseases commonly fewer than 10% of monarch eggs and caterpillars survive.[6]:(pp21-22)

Pupa[edit]

In the pupa or chrysalis stage, the caterpillar spins a silk pad onto a horizontal substrate. It then hangs from the pad by the last pair of prolegs upside down resembling the letter 'J'. It sheds its skin leaving itself encased in an articulated green exoskeleton. During this pupal stage, the adult butterfly forms inside. The exoskeleton becomes transparent before it ecloses (emerges), and its adult colors can be seen.

Adult[edit]

The adult butterfly emerges after about two weeks, and hangs until its wings are dry. Fluids are pumped into wings and they expand and stiffen. The monarch expands and retracts its wings, and when conditions allow it then flies to feed on a variety of nectar plants. During the breeding season adults reach sexual maturity in four or five days, however, the migrating generation will not reach maturity until overwintering is complete.[30] Monarchs typically live two to five weeks during the breeding season.[6]:(pp22-23) Larvae growing in high densities are smaller, have lower survival, and weigh less as adults compared to lower densities.[31]

Reproduction[edit]

Monarch butterfly mating

Males who are fit are more likely to mate. Females and males typically mate more than once. Females that mate several times lay more eggs.[32] Mating for the overwintering populations occurs in the spring, prior to dispersion. Mating is less dependent on pheromones than other species in its genus.[33]

Courtship occurs in two phases. During the aerial phase, the male pursues and often forces the female to the ground. During the ground phase, the butterflies copulate and remain attached for about 30 to 60 minutes.[34] Only 30% of mating attempts end in copulation, suggesting that females may be able to avoid mating though some have more success than others.[35][36] During copulation, the male transfers the spermatophore to the female. Along with sperm, the spermatophore provides the female with nutrition to aid her in egg-laying. An increase in spermatophore size increases the fecundity of female monarchs. Males that produce larger spermatophores also fertilize more female's eggs.[37]

Pictorial lifecycle[edit]

Taxonomy[edit]

White morph of the monarch in Hawaii called White Monarch.

The name 'monarch' may be in honor of King William III of England.[38] The monarch was originally described by Linnaeus in his Systema Naturae of 1758 and it was placed in the genus Papilio.[39] In 1780, Jan Krzysztof Kluk used the monarch as the type species for a new genus; Danaus.

There are three species of Monarch butterflies:

  • D. plexippus, described by Linnaeus in 1758, is the species known most commonly as the monarch butterfly of North America. Its range actually extends worldwide and can be found in Hawaii, Australia, New Zealand, Spain and on Oceanic Islands.
  • D. erippus, the southern monarch was described by Cramer in 1775, This species is found in tropical and subtropical latitudes of South America, mainly in Brazil, Uruguay, Paraguay, Argentina, Bolivia, Chile and southern Peru. The south American monarch and the North American monarch may have been one species at one time. Some researchers believe the southern monarch separated from the monarch's population some 2 mya, at the end of the Pliocene. Sea levels were higher and the entire Amazonas lowland was a vast expanse of brackish swamp that offered limited butterfly habitat.[40]

Six subspecies and two color morphs of D. plexippus have been identified:[42]

  • D. p. plexippus – nominate subspecies, described by Linnaeus in 1758, is the migratory subspecies known from most of North America
    • D. p. p. form nivosus, the white monarch commonly found on Oahu, Hawaii and rarely in other locations.[11]
    • D. p. p. (as yet unnamed) – a color morph lacking some wing vein markings[43]

The percentage the white morph in Oahu, is nearing 10%. On other Hawaiian islands, the white morph occurs at a relatively low frequency. White Monarchs (nivosus) have been found throughout the world, including Australia, New Zealand, Indonesia, and the United States.[11]

Some taxonomists disagree on these classifications.[40][44]

Monarchs were classified under the family Danaidae, but have been re-classified under Nymphalidae since at least 1958.[45]

Larvae host plants[edit]

The host plants used by the monarch caterpillar include:

Swamp milkweed, one of many species of Asclepias milkweeds used by the monarch

North America[edit]

Asclepias curassavica has been planted as an ornamental and naturalized. Its distribution is probably worldwide. Year-round plantings may be the cause of new overwintering sites along the Gulf coast and in Spain.

Adult food sources[edit]

Nectaring on purple coneflower Echinacea purpurea.

Although larvae eat only milkweed, adult monarchs feed on the nectar of many plants including:

Monarchs obtain moisture and minerals from damp soil and wet gravel, a behavior known as mud-puddling. The monarch has also been noticed puddling at an oil stain on pavement.[24]

Origin of name[edit]

Danaus (Greek Δαναός), a great-grandson of Zeus, was a mythical king in Egypt or Libya, who founded Argos; Plexippus was one of the 50 sons of Aegyptus, the twin brother of Danaus.

In Homeric Greek plexippos (πληξιππος) means "one who urges on horses", i.e. "rider or charioteer". In the 10th edition of Systema Naturae, at the bottom of page 467,[49] Linnaeus wrote that the names of the Danai festivi, the division of the genus to which Papilio plexippus belonged, were derived from the sons of Aegyptus. Linnaeus divided his large genus Papilio, containing all known butterfly species, into what we would now call subgenera. The Danai festivi formed one of the 'subgenera', containing colourful species, as opposed to the Danai candidi, containing species with bright white wings. Linnaeus wrote: "Danaorum Candidorum nomina a filiabus Danai Aegypti, Festivorum a filiis mutuatus sunt." (= The names of the Danai candidi have been derived from the daughters of Danaus, those of the Danai festivi from the sons of Aegyptus).

Robert Michael Pyle suggested Danaus is a masculinised version of Danaë (Greek Δανάη), Danaus’s great-great-granddaughter, to whom Zeus came as a shower of gold, which seemed to him a more appropriate source for the name of this butterfly.[50] He masculinized the genus name because it had to agree in gender with the species name. If the species-group name is not a noun in apposition, Pyle could have been right and the genus name and specific epithet have to agree in gender, but in that case it is the specific epithet and not the genus name, that is to be altered. In the case of Danaus plexippus, however, the specific epithet is a noun in apposition, formed from a personal name in the nominative case, which should not be altered (see ICZN art. 31.1 and art. 32.3). If, instead of Danaus, Danaë had been intended, the name would simply have been Danae plexippus. Moreover, in Systema Naturae, there is a very strong connection of the names with Danaus, and not a single one with Danaë.

Migration[edit]

The eastern population migrates both north and south on an annual basis. The population east of the Rocky Mountains migrates to the sanctuaries of the Mariposa Monarca Biosphere Reserve in Mexico. The western population overwinters in various coastal sites in central and southern California. The overwintered population of those east of the Rockies may reach as far north as Texas and Oklahoma during the spring migration. The second, third and fourth generations return to their northern locations in the United States and Canada in the spring.[51] Commercially bred monarchs migrate to overwintering sites in Mexico adding to already existing data of migratory behavior. Not all monarchs in the eastern population migrate to Mexico.[52]

Defense against predators[edit]

In both caterpillar and butterfly form, monarchs are aposematic—warding off predators with a bright display of contrasting colors to warn potential predators of their undesirable taste and poisonous characteristics.

Large larvae are able to avoid wasp predation by dropping from the plant or by jerking their bodies.[53]

Aposematism

Chemical structure of oleandrin, one of the cardiac glycosides

Monarchs are foul-tasting and poisonous due to the presence of cardenolide aglycones in their bodies, which the caterpillars ingest as they feed on milkweed.[33] By ingesting a large amount of plants in the genus Asclepias, primarily milkweed, monarch caterpillars are able to sequester cardiac glycosides, or more specifically cardenolides, which are steroids that act in heart-arresting ways similar to digitalis.[54] It has been found that monarchs are able to sequester cardenolides most effectively from plants of intermediate cardenolide content rather than those of high or low content.[55]

Additional studies have shown that different species of milkweed have differing effects on growth, virulence, and transmission of parasites.[56] One species, Asclepias curassavica, appears to reduce the proportion of monarchs infected by parasites. There are two possible explanations for the positive role of A. curassavica on the monarch caterpillar: that it promotes overall monarch health to boost the monarch's immune system; or that chemicals from the plant have a direct negative effect on the parasites.[56]

After the caterpillar becomes a butterfly, the toxin shift to different parts of the body. Since many birds attack the wings of the butterfly, having three times the cardiac glycosides in the wings leaves predators with a very foul taste, and may prevent them from ever ingesting the body of the butterfly.[54] In order to combat predators that remove the wings only to ingest the abdomen, monarchs keep the most potent cardiac glycosides in their abdomens.[57]

Mimicry

Monarch (left) and viceroy (right) butterflies exhibiting Müllerian mimicry

Monarchs share the defense of noxious taste with the similar-appearing viceroy butterfly in what is perhaps one of the most well-known examples of mimicry. Though long purported to be an example of Batesian mimicry, the viceroy is actually reportedly more unpalatable than the monarch, making this a case of Müllerian mimicry.[58]

Human Interactions[edit]

The monarch is the state insect of Alabama,[59] Idaho,[60] Illinois,[61] Minnesota,[62] Texas,[63] Vermont,[64] and West Virginia.[65] It was nominated in 1990 as the national insect of the United States of America.[66] but the legislation did not pass.[67]

Monarchs can be attracted by cultivating a butterfly garden with specific milkweed species and nectar plants. Efforts are underway to establish these Monarch Waystations.[68] Monarchs are raised as a hobby and for educational purposes.[69]

An IMAX film, Flight of the Butterflies, describes the story of the Urquharts, Brugger and Trail to then unknown migration to Mexican overwintering areas.[70]

Sanctuaries and reserves have been created at over-wintering locations in Mexico and California to limit habitat destruction. These sites can generate significant tourism revenue. [71]

Organizations and individuals participate in tagging programs. Tagging information is used to study migration patterns.[72]

Monarchs are bred and used in schools, hospices, memorial services and weddings.[73] Memorial services for 911 include the release of captive bred monarchs.[74][75][76] Monarchs are used in schools and nature centers for educational purposes.[77]

Threats[edit]

Predators[edit]

Larva feed exclusively on milkweed and consume protective cardiac glycosides. Toxin levels in Asclepias sp.vary. Not all monarchs are unpalatable, but exhibit Batesian or automimics. Cardiac glycosides levels are higher in the abdomen and wings. Some predators can differentiate between these parts and consume the most palatable ones.[78] Bird predators include brown thrashers, grackles, robins, cardinals, sparrows, scrub jays, pinyon jays,[78]Black-headed Grosbeak, and orioles.[18]

Some mice are able to withstand large doses of the toxin. Overwintering adults become less toxic over time making them more vulnerable to predators. In Mexico, about 14% of the overwintering monarchs are eaten by birds and mice.[23]

In North America, eggs and first instar larvae of the monarch are eaten by larvae and adults of the introduced Asian lady beetle (Harmonia axyridis).[79] The Chinese mantis ("Tenodera sinensis") will consume the larvae once the gut is removed thus avoiding cardenolides.[80] Wasps commonly consume larvae.[81]

Several birds have also adapted various methods that allow them to ingest monarchs without experiencing the ill effects associated with the cardiac glycosides. The oriole is able to eat the monarch through an exaptation of its feeding behavior that gives it the ability to identify cardenolides by taste and reject them.[82] The grosbeak, on the other hand, has adapted the ability an insensitivity to secondary plant poisons which allows it to ingest monarchs without vomiting. As a result, orioles and grosbeaks will periodically have high levels of cardenolides in their bodies, and they will be forced to go on periods of reduced monarch consumption. This cycle of predation effectively reduces the potential predation of monarchs by 50 percent and indicates that monarch aposematism has a legitimate purpose.[82]

On Oahu, a white morph of the monarch has emerged. This is because of the introduction, in 1965 and 1966, of two bulbul species, Pycnonotus cafer and Pycnonotus jocosus. They are now the most common insectivore birds, and probably the only ones preying on insects as large as the monarch. Monarchs in Hawaii are known to have low cardiac glycoside levels, but the birds may also be tolerant of the chemical. The two species hunt the larvae and some pupae from the branches and undersides of leaves in milkweed bushes. The bulbuls also eat resting and ovipositing adults, but rarely flying ones. Because of its colour, the white morph has a higher survival rate than the orange one. This is either because of apostatic selection (i.e. the birds have learned the orange monarchs can be eaten), because of camouflage (the white morph matches the white pubescence of milkweed or the patches of light shining through foliage), or because the white morph does not fit the bird's search image of a typical monarch, so is thus avoided.[83]

Parasites[edit]

Parasites include the tachinid flies Sturmia convergens[84] and Lespesia archippivora. Lesperia-parasitized butterfly larvae complete the formation of their crysalid but die before they emerge as an adult. Before pupation is complete, one white maggot comes out of the chrysalid. The maggot forms a brown pupa on the ground then emerges as an adult.[85]

The bacterium Micrococcus flacidifex danai also infects larvae. Just before pupation, the larvae migrate to a horizontal surface and die a few hours later, attached only by one pair of prolegs, with the thorax and abdomen hanging limp. The body turns black shortly after. The bacterium Pseudomonas aeruginosa has no invasive powers, but causes secondary infections in weakened insects. It is a common cause of death in laboratory-reared insects.[85]

The protozoan Ophryocystis elektroscirrha is another parasite of the monarch. It infects the subcutaneous tissues and propagates by spores formed during the pupal stage. The spores are found over all of the body of infected butterflies, with the greatest number on the abdomen. These spores are passed, from female to caterpillar, when spores rub off during egg-laying and are then ingested by caterpillars. Severely infected individuals are weak, unable to expand their wings, or unable to eclose, and have shortened lifespans, but parasite levels variy in populations. This is not the case in laboratory rearing, where after a few generations, all individuals can be infected.[86] Infection with this parasite creates an effect known as culling whereby migrating monarchs that are infected are less likely to complete the migration. This results in overwintering populations with lower parasite loads.[87]

Confusion of host plants[edit]

The black swallow-wort (Cynanchum louiseae) and pale swallow-wort (Cynanchum rossicum) plants are problematic for monarchs in North America. Monarchs lay their eggs on these relatives of native vining milkweed (Cynanchum laeve) because they produce stimuli similar to milkweed. Once the eggs hatch, the caterpillars are poisoned by the toxicity of this invasive plant from Europe.[88]

Population decline[edit]

Populations counts show a decline in Monarch populations at their overwintering sites. Though most researchers accept these data it has currently come into question.[89]

The yearly decrease in the monarch butterfly population has been linked to the decrease in the milkweed plant (Asclepias)—a primary food for monarchs—from herbicide use in the butterfly’s reproductive and feeding areas. The destruction of common milkweed has effectively eliminated the food source from most of the habitat monarchs used to use.[90] Common milkweed is susceptible to the use of herbicides. Varietals do exist, however, (see Human Interactions) that can be successfully planted in gardens and other areas to help mitigate habitat loss in the wild.[91]

Habitat loss due to herbicide use[edit]

Conservationists attribute the disappearance of mikweed speices to agricultural practices in the Midwest, where genetically modified seeds are bred to resist herbicides that eliminate milkweed nearby. Growers eliminate milkweed that previously grew between the rows of food crops. Corn and soybeans are resistant to the effect of the herbicide glyphosate. The increased use of these crop strains is correlated with the decline in Monarch populations between 1999 and 2010.[92][93] Chip Taylor, director of Monarch Watch at the University of Kansas, said the Midwest milkweed habitat "is virtually gone" with 120–150 million acres lost.[94][95] To help fight this problem, Monarch Watch encourages the planting of “Monarch Waystations.” [96] Garden-friendly milkweed not only helps fight the declining Monarch population, but also encourages other pollinators as well.[91]

A letter published in Nature proposed that pollen from genetically modified maize could deposit onto larval food plants, Asclepias spp. (milkweed), increasing mortality of the larva.[97]

Loss of overwintering habitat[edit]

The area of forest occupied has been declining and reached its lowest level in two decades in 2013. The decline is continuing but is expected to increase during the 2013–2014 season.

Mexican environmental authorities continue to monitor illegal logging of the oyamel trees. The Oyamel is a major species of evergreen on which the overwintering butterflies spend a significant time during their winter diapause.[98]

Climate[edit]

Climate variations during the fall and summer affect butterfly reproduction. Rainfall, and freezing temperatures affect milkweed growth. Omar Vidal, director general of WWF-Mexico, said "The monarch’s lifecycle depends on the climatic conditions in the places where they breed. Eggs, larvae and pupae develop more quickly in milder conditions. Temperatures above 95°F can be lethal for larvae, and eggs dry out in hot, arid conditions, causing a drastic decrease in hatch rate." [99]

Genome[edit]

The monarch was the first butterfly to have its genome sequenced.[6]:(p12) The 273-million base pair draft sequence includes a set of 16,866 protein-coding genes. The genome provides researchers insights into migratory behavior, the circadian clock, juvenile hormone pathways and microRNAs that are differentially expressed between summer and migratory monarchs.[100][101][102] More recently, the genetic basis of monarch migration and warning coloration has been described.[103]

There is no genetic differentiation between the migratory populations of eastern and western North America.[6]:(p16) Recent research has identified the specific areas in the genome of the monarch that regulate migration. There appears to be no genetic difference between a migrating and nonmigrating monarch but the gene is expressed in migrating monarchs but not expressed in nonmigrating monarchs.[21]

Conservation[edit]

The Center for Biological Diversity, The Center for Food Safety, The Xerces Society and Lincoln Brower have filed a petition to the United States Department of the Interior to protect the monarch by having it declared an endangered species.[6]

Conservationists are lobbying transportation departments and utilities to reduce their use of herbicides and specifically encourage milkweed to grow along roadways and power lines. Reducing roadside mowing and application of herbicides during the butterfly breeding season will encourage milkweed growth. Conservationists lobby agriculture companies to set aside areas that remain unsprayed to allow the butterflies to breed.[93] Butterfly gardening is thought to increase the populations of butterflies.[104]

See also[edit]

References[edit]

  1. ^ Committee On Generic Nomenclature, Royal Entomological Society of London (2007) [1934]. The Generic Names of British Insects. Royal Entomological Society of London Committee on Generic Nomenclature, Committee on Generic Nomenclature. British Museum (Natural History). Dept. of Entomology. p. 20. 
  2. ^ Scudder, Samuel H.; William M. Davis; Charles W. Woodworth; Leland O. Howard; Charles V. Riley; Samuel W. Williston (1989). The butterflies of the eastern United States and Canada with special reference to New England. The author. p. 721. ISBN 0-665-26322-8. 
  3. ^ a b Garber, Steven D. (1998). The Urban Naturalist. Courier Dover Publications. pp. 76–79. ISBN 0-486-40399-8. 
  4. ^ Groth, Jacob (10 November 2000). "Monarch Migration Study". Swallowtail Farms. Retrieved 21 July 2014. 
  5. ^ "Monarch Migration". Monarch Joint Venture. 2013. 
  6. ^ a b c d e f g h i j k l m "Petition to protect the Monarch butterfly (Danaus plexippus plexippus) under the endangered species act". Xerces Society. Retrieved 1 September 2014. 
  7. ^ a b Braby, Michael F. (2000). Butterflies of Australia: Their Identification, Biology and Distribution. CSIRO Publishing. pp. 597–599. ISBN 0-643-06591-1. 
  8. ^ Satterfield, Dara A.; Davis, Andrew K. (April 2014). "Variation in wing characteristics of monarch butterflies during migration: Earlier migrants have redder and more elongated wings". Animal Migration 2 (1). doi:10.2478/ami-2014-001 (inactive 2014-12-15). 
  9. ^ Klots, Alexander B. (1951). A Field Guide to the Butterflies of North America, East of the Great Plains (Tenth ed.). Boston: Houghton Mifflin Company. pp. 78, 79. ISBN 0395078652. 
  10. ^ "Monarch, Danaus plexippus". Retrieved 27 August 2008. 
  11. ^ a b c Gibbs, Lawrence; Taylor, O.R. (1998). "The White Monarch". Department of Entomology University of Kansas. Retrieved 17 July 2014. 
  12. ^ Darby, Gene (1958). What is a Butterfly. Chicago: Benefic Press. p. 10. 
  13. ^ Gerald McCormack (7 December 2005). "Cook Islands' Largest Butterfly – the Monarch". Cook Islands Biodiversity. 
  14. ^ Davis, Donald (27 November 2014). "DPLEX-L:59250 THE possibility of a trans-Gulf migration, oil rigs, Dr. Gary Ross, and more". Dplex mailing list. Monarch Watch, University of Kansas.
  15. ^ "Monarch Sightings Map". Monarch Butterfly New Zealand Trust. Retrieved 15 December 2014. 
  16. ^ "The lonely flight of the monarch butterfly". NewsAdvance.com, Lynchburg, Virginia Area. Retrieved 7 October 2014. 
  17. ^ Pais, Miguel. "Northwestern African sightings of D.plexippus, Maroc>Pappilons>Danaus plexippus". Google Maps. Retrieved 19 September 2014. 
  18. ^ a b c Scott, James A. (1986). The Butterflies of North America. Stanford University Press, Stanford, CA. ISBN 0-8047-2013-4
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