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?Butterflies
Cairns Birdwing, the largest butterfly in Australia (Melbourne Zoo).
Cairns Birdwing, the largest butterfly in Australia (Melbourne Zoo).
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
(unranked) Rhopalocera
Superfamilies and families

A butterfly is an insect of the order Lepidoptera. Like all Lepidoptera, butterflies are notable for their unusual life cycle with a larval caterpillar stage, an inactive pupal stage, and a spectacular metamorphosis into a familiar and colourful winged adult form. Most species are day-flying so they regularly attract attention. The diverse patterns formed by their brightly coloured wings and their erratic yet graceful flight have made butterfly watching a fairly popular hobby.

Butterflies comprise the true butterflies (superfamily Papilionoidea), the skippers (Superfamily Hesperioidea) and the moth-butterflies (Superfamily Hedyloidea). Butterflies exhibit polymorphism, mimicry and aposematism. Some are known to migrate over large distances. Some butterflies have evolved symbiotic and parasitic relationships with social insects such as ants. Butterflies are important economically as one of the major agents of pollination. In addition, a number of species are pests, because they can damage domestic crops and trees.

Culturally, butterflies are a popular motif in the visual and literary arts.

Origin and distributionEdit

Butterflies are nested within the evolutionary tree of moths. Their origins may date back to the Cretaceous Period, ending 65 million years ago.[1] Unfortunately, the fossil record is very limited. The oldest known fossil is an unnamed possible skipper butterfly from the Upper Palaeocene (around 57 million year old) of Fur, Denmark [2]. One of the most beautifully preserved is a Metalmark butterfly (Voltinia dramba) from 25 million year old Dominican amber[3].

Butterflies are today distributed throughout the world except in the very cold and arid regions. There are an estimated 17,500 species of butterflies (Papilionoidea) out of about 180,000 species of Lepidoptera.[4]

ClassificationEdit

 
Rhopalocera
Papilionoidea

Papilionidae



 

Pieridae


 


Riodinidae



Lycaenidae




Nymphalidae





Hesperiidae
 

Coeliadinae




Euschemoninae




Eudaminae



 

Pyrginae


 

Heteropterinae




Trapezitinae



Hesperiinae









Hedylidae




Phylogeny of the group.[5]
Blue morpho butterfly

Blue Morpho, Family Nymphalidae

File:Meadow Argus02.jpg

Presently butterflies are classified in three superfamilies, Hedyloidea, consisting of the 'American moth-butterflies', Hesperioidea, consisting of the 'skippers' and Papilionoidea or 'true butterflies'. The last two superfamilies are probably sister taxa, so the butterflies collectively are thought to constitute a natural group or clade.

The scope of the term butterfly depends on how far the concept is extended. Currently, most experts include the superfamilies Hedyloidea (the American moth-butterflies), Hesperioidea (the skippers) and Papilionoidea (the so-called 'true' butterflies). This concept of butterflies including the Hedyloidea is a recently expanded one, but it makes the group a natural clade, the Rhopalocera.[6]

Butterfly familiesEdit

The five families of true butterflies usually recognized in the Papilionoidea are:-

The superfamily Hesperioidea comprises one family only, albeit a large one, the skippers of family Hesperiidae, whereas the superfamily Hedyloidea also consists of a single family Hedylidae with about 40 species.[7]

Taxonomic issuesEdit

A study combining morphological and molecular data concluded that Hesperiidae, Papilionidae, Pieridae, Lycaenidae and Riodinidae could all be strongly supported as monophyletic groups, but the monophyletic status of Nymphalidae is uncertain. Lycaenidae and Riodinidae were confirmed as sister taxa, and Papilionidae as the outgroup to the rest of the true butterflies, but the location of Pieridae within the pattern of descent was unclear, with different lines of evidence suggesting different conclusions. The data suggested that the Hedyloidea are indeed more closely related to the butterflies than to other moths.[8]

Some older classifications recognize additional families, for example Danaidae, Heliconiidae, Libytheidae and Satyridae, but modern classifications treat these as subfamilies within the Nymphalidae.

Butterflies and mothsEdit

Main article: Differences between butterflies and moths

The dichotomous classification of lepidopterans into butterflies and moths is one that is popular but not used in taxonomy. The folk groups of butterflies and moths can be distinguished using several features but there are exceptions to most of these rules.

The four stages in the lifecycle of a butterflyEdit

File:Mating Common Buckeyes.jpg

Unlike many insects, butterflies do not experience a nymph period, but instead go through a pupal stage which lies between the larva and the adult stage (the imago). Butterflies are termed as holometabolous insects, and go through complete metamorphosis.

It is a popular belief that butterflies have very short life spans. However, butterflies in their adult stage can live from a week to nearly a year depending on the species. Many species have long larval life stages while others can remain dormant in their pupal or egg stages and thereby survive winters.[9]

Butterflies may have one or more broods per year. The number of generations per year varies from temperate to tropical regions with tropical regions showing a trend towards multivoltinism.

EggEdit

File:Ariadne merione egg sec.jpg

Butterfly eggs consist of a hard-ridged outer layer of shell, called the chorion. This is lined with a thin coating of wax which prevents the egg from drying out before the larva has had time to fully develop. Each egg contains a number of tiny funnel-shaped openings at one end, called micropyles; the purpose of these holes is to allow sperm to enter and fertilize the egg. Butterfly and moth eggs vary greatly in size between species, but they are all either spherical or ovate.

Butterfly eggs are fixed to a leaf with a special glue which hardens rapidly. As it hardens it contracts, deforming the shape of the egg. This glue is easily seen surrounding the base of every egg forming a meniscus. The nature of the glue is unknown and is a suitable subject for research. The same glue is produced by a pupa to secure the setae of the cremaster. This glue is so hard that the silk pad, to which the setae are glued, cannot be separated.

Eggs are usually laid on plants. Each species of butterfly has its own hostplant range and while some species of butterfly are restricted to just one species of plant, others use a range of plant species, often including members of a common family.

The egg stage lasts a few weeks in most butterflies but eggs laid close to winter, especially in temperate regions, go through a diapause stage, and the hatching may take place only in spring. Other butterflies may lay their eggs in the spring and have them hatch in the summer. These butterflies are usually northernly species (Mourning cloak, Tortoiseshells)

CaterpillarsEdit

File:Lycaenid ant sec.jpg

Larvae, or caterpillars, are multi-legged eating machines. They consume plant leaves and spend practically all of their time in search of food. Although most caterpillars are herbivorous, a few species such as Spalgis epius and Liphyra brassolis are entomophagous (insect eating). Some larvae, especially those of the Lycaenidae form mutual associations with ants. They communicate with the ants using vibrations that are transmitted through the substrate as well as using chemical signals.[10][11] The ants provide some degree of protection to these larvae and they in turn gather honeydew secretions.

Caterpillars mature through a series of stages, called instars. Near the end of each instar, the larva undergoes a process called apolysis, in which the cuticle, a mixture of chitin and specialized proteins, is released from the epidermis and the epidermis begins to form a new cuticle beneath. At the end of each instar, the larva moults the old cuticle, and the new cuticle rapidly hardens and pigments. Development of butterfly wing patterns begins by the last larval instar.

Butterfly caterpillars have three pairs of true legs from the thoracic segments and up to 6 pairs of prolegs arising from the abdominal segments. These prolegs have rings of tiny hooks called crochets that help them grip the substrate.

Some caterpillars have the ability to inflate parts of their head to appear snake-like. Many have false eye-spots to enhance this effect. Some caterpillars have special structures called osmeteria which are everted to produce smelly chemicals. These are used in defense.

Host plants often have toxic substances in them and caterpillars are able to sequester these substances and retain them into the adult stage. This helps making them unpalatable to birds and other predators. Such unpalatibility is advertised using bright red, orange, black or white warning colours. The toxic chemicals in plants are often evolved specifically to prevent them from being eaten by insects. Insects in turn develop countermeasures or make use of these toxins for their own survival. This "arms race" has led to the coevolution of insects and their host plants.[12]

Wing developmentEdit

File:Butterfly wing closeup.jpg
File:Fifthinstarwingdisk.png

Wings or wing pads are not visible on the outside of the larva, but when larvae are dissected, tiny developing wing disks can be found on the second and third thoracic segments, in place of the spiracles that are apparent on abdominal segments. Wing disks develop in association with a trachea that runs along the base of the wing, and are surrounded by a thin peripodial membrane, which is linked to the outer epidermis of the larva by a tiny duct.

Wing disks are very small until the last larval instar, when they increase dramatically in size, are invaded by branching tracheae from the wing base that precede the formation of the wing veins, and begin to develop patterns associated with several landmarks of the wing.

Near pupation, the wings are forced outside the epidermis under pressure from the hemolymph, and although they are initially quite flexible and fragile, by the time the pupa breaks free of the larval cuticle they have adhered tightly to the outer cuticle of the pupa (in obtect pupae). Within hours, the wings form a cuticle so hard and well-joined to the body that pupae can be picked up and handled without damage to the wings.

PupaEdit

File:Pupation - Inachis io.jpg
File:Chrysalis5504.jpg

When the larva is fully grown, hormones such as prothoracicotropic hormone (PTTH) are produced. At this point the larva stops feeding and begins "wandering" in the quest of a suitable pupation site, often the underside of a leaf.

The larva transforms into a pupa (or chrysalis) by anchoring itself to a substrate and moulting for the last time. The chrysalis is usually incapable of movement, although some species can rapidly move the abdominal segments or produce sounds to scare potential predators.

The pupal transformation into a butterfly through metamorphosis has held great appeal to mankind. To transform from the miniature wings visible on the outside of the pupa into large structures usable for flight, the pupal wings undergo rapid mitosis and absorb a great deal of nutrients. If one wing is surgically removed early on, the other three will grow to a larger size. In the pupa, the wing forms a structure that becomes compressed from top to bottom and pleated from proximal to distal ends as it grows, so that it can rapidly be unfolded to its full adult size. Several boundaries seen in the adult color pattern are marked by changes in the expression of particular transcription factors in the early pupa.

Adult or ImagoEdit

The adult, sexually mature, stage of the insect is known as the imago. As Lepidoptera, butterflies have four wings that are covered with tiny scales (see photo). The fore and hindwings are not hooked together, permitting a more graceful flight. An adult butterfly has six legs, but in the nymphalids, the first pair is reduced. After it emerges from its pupal stage, a butterfly cannot fly until the wings are unfolded. A newly-emerged butterfly needs to spend some time inflating its wings with blood and letting them dry, during which time it is extremely vulnerable to predators. Some butterflies' wings may take up to three hours to dry while others take about one hour. Most butterflies and moths will excrete excess dye after hatching. This fluid may be white, red, orange, or in rare cases, blue.

External morphologyEdit

Main article: Glossary of Lepidopteran terms



ScalesEdit

File:Microphoto-butterflywing.jpg

Butterflies are characterized by their scale-covered wings. The coloration of butterfly wings is created by minute scales. These scales are pigmented with melanins that give them blacks and browns, but blues, greens, reds and iridescence are usually created not by pigments but the microstructure of the scales. This structural coloration is the result of coherent scattering of light by the photonic crystal nature of the scales.[13][14][15]

PolymorphismEdit

Many adult butterflies exhibit polymorphism, showing differences in appearance. These variations include geographic variants and seasonal forms. In addition many species have females in multiple forms, often with mimetic forms. Sexual dimorphism in coloration and appearance is widespread in butterflies. In addition many species show sexual dimorphism in the patterns of ultraviolet reflectivity, while otherwise appearing identical to the unaided human eye. Most of the butterflies have a sex-determination system that is represented as ZW with females being the heterogametic sex (ZW) and males homogametic (ZZ).[16]

Genetic abnormalities such as gynandromorphy also occur from time to time. In addition many butterflies are infected by Wolbachia and infection by the bacteria can lead to the conversion of males into females[17] or the selective killing of males in the egg stage.[18]

MimicryEdit

File:Heliconius mimicry.png

Batesian and Mullerian mimicry in butterflies is common. Batesian mimics imitate other species to enjoy the protection of an attribute they do not share, aposematism in this case. The Common Mormon of India has female morphs which imitate the unpalatable red-bodied swallowtails, the Common Rose and the Crimson Rose. Mullerian mimicry occurs when aposematic species evolve to resemble each other, presumably to reduce predator sampling rates, the Heliconius butterflies of the Americas being a good example.

Wing markings called eyespots are present in some species; these may have an automimicry role for some species. In others, the function may be intraspecies communication, such as mate attraction. In several cases, however, the function of butterfly eyespots is not clear, and may be an evolutionary anomaly related to the relative elasticity of the genes that encode the spots.[20][21]

Seasonal polyphenismEdit

<div name="wet-dry forms"/>Many of the tropical butterflies have distinctive seasonal forms. This phenomenon is termed seasonal polyphenism and the seasonal forms of the butterflies are called the dry-season and wet-season forms. How the season affects the genetic expression of patterns is still a subject of research.[22] Experimental modification by ecdysone hormone treatment has demonstrated that it is possible to control the continuum of expression of variation between the wet and dry-season forms.[23] The dry-season forms are usually more cryptic and it has been suggested that the protection offered may be an adaptation. Some also show greater dark colours in the wet-season form which may have thermoregulatory advantages by increasing ability to absorb solar radiation.[24]

HabitsEdit

File:Australian painted lady feeding.jpg
File:Monarch In May.jpg

Butterflies feed primarily on nectar from flowers. Some also derive nourishment from pollen, tree sap, rotting fruit, dung, and dissolved minerals in wet sand or dirt. Butterflies play an important ecological role as pollinators.

As adults, butterflies consume only liquids and these are sucked by means of their proboscis. They feed on nectar from flowers and also sip water from damp patches. This they do for water, for energy from sugars in nectar and for sodium and other minerals which are vital for their reproduction. Several species of butterflies need more sodium than provided by nectar. They are attracted to sodium in salt and they sometimes land on people, attracted by human sweat. Besides damp patches, some butterflies also visit dung, rotting fruit or carcasses to obtain minerals and nutrients. In many species, this Mud-puddling behaviour is restricted to the males and studies have suggested that the nutrients collected are provided as a nuptial gift along with the spermatophore during mating.[25]

Butterflies sense the air for scents, wind and nectar using their antennae. The antennae come in various shapes and colours. The hesperids have a pointed angle or hook to the antennae, while most other families show knobbed antennae. The antennae are richly covered with sensillae. A butterfly's sense of taste is coordinated by chemoreceptors on the tarsi, which work only on contact, and are used to determine whether an egg-laying insect's offspring will be able to feed on a leaf before eggs are laid on it[26]. Many butterflies use chemical signals, pheromones, and specialized scent scales (androconia) and other structures (coremata or 'Hair pencils' in the Danaidae) are developed in some species.

File:Antennae ctb.png

Vision is well developed in butterflies and most species are sensitive to the ultraviolet spectrum. Many species show sexual dimorphism in the patterns of UV reflective patches.[27] Color vision may be widespread but has been demonstrated in only a few species.[28][29]

Some butterflies have organs of hearing and some species are also known to make stridulatory and clicking sounds.[30]

Many butterflies, such as the Monarch butterfly, are migratory and capable of long distance flights. They migrate during the day and use the sun to orient themselves. They also perceive polarized light and use it for orientation when the sun is hidden.[31]

Many species of butterfly maintain territories and actively chase other species or individuals that may stray into them. Some species will bask or perch on chosen perches. The flight styles of butterflies are often characteristic and some species have courtship flight displays. Basking is an activity which is more common in the cooler hours of the morning. Many species will orient themselves to gather heat from the sun. Some species have evolved dark wingbases to help in gathering more heat and this is especially evident in alpine forms.[32]

FlightEdit

Like many other members of the insect world, the lift generated by butterflies is more than what can be accounted for by steady-state, non-transitory aerodynamics. Studies using Vanessa atalanta in a windtunnel show that they use a wide variety of aerodynamic mechanisms to generate force. These include wake capture, vortices at the wing edge, rotational mechanisms and Weis-Fogh 'clap-and-fling' mechanisms. The butterflies were also able to change from one mode to another rapidly.[33] (See also Insect flight)

MigrationEdit

See also Insect migration

Many butterflies migrate over long distances. Particularly famous migrations being those of the Monarch butterfly from Mexico to North America, a distance of about 4,000 to 4,800 kilometres (2500-3000 miles). Other well known migratory species include the Painted Lady and several of the Danaine butterflies. Spectacular and large scale migrations associated with the Monsoons are seen in peninsular India.[34] Migrations have been studied in more recent times using wing tags and also using stable hydrogen isotopes.[35][36]

Butterflies have been shown to navigate using time compensated sun compasses. They can see polarized light and therefore orient even in cloudy conditions. The polarized light in the region close to the ultraviolet spectrum is suggested to be particular important.[37]

It is suggested that most migratory butterflies are those that belong to semi-arid areas where breeding seasons are short.[38] The life-histories of their host plants also influence the strategies of the butterflies.[39]

DefenseEdit

Butterflies are threatened in their early stages by parasitoids and in all stages by predators, diseases and environmental factors. They protect themselves by a variety of means.

Chemical defenses are widespread and are often based on chemicals of plant origin. In many cases the plants themselves have evolved these toxic substances to reduce attack to them. These defense mechanisms are effective only if they are also well advertised. Many unpalatable butterflies are brightly colored. This has led to unprotected butterflies evolving forms that appear like the unpalatable butterflies. These mimetic forms are usually restricted to the females.

File:Butterfly Eyespot.JPG

Cryptic coloration is found in many butterflies. Some like the oakleaf butterfly are remarkable imitations of leaves.[40] As caterpillars, many defend themselves by freezing and appearing like sticks or branches. Some papilionid caterpillars resemble bird dropping in their early instars. Some caterpillars have hairs and bristly structures that provide protection while others are gregarious and form dense aggregations. Some species also form associations with ants and gain their protection (See Myrmecophile).

Behavioural defenses include perching and wing positions to avoid being conspicuous. Some female Nymphalid butterflies are known to guard their eggs from parasitoid wasps.[41]

Eyespots and tails are found in many lycaenid butterflies and these divert the attention of predators from the more vital head region. An alternative theory is that these cause ambush predators such as spiders to approach from the wrong end and allow for early visual detection.[42]

Notable SpeciesEdit

There are between 15,000 and 20,000 species of butterflies worldwide. Some well known species from around the world include:

In cultureEdit

ArtEdit

File:Carl Spitzweg 033.jpg

Artistic depictions of butterflies have been used in many cultures including Egyptian hieroglyphics 3500 years ago.[43] Today, butterflies are widely used in various objects of art.

SymbolismEdit

According to the “Butterflies” chapter in Kwaidan: Stories and Studies of Strange Things, by Lafcadio Hearn, a butterfly is seen as the personification of a person's soul; whether they be living, dying, or already dead. One Japanese superstition says that if a butterfly enters your guestroom and perches behind the bamboo screen, the person whom you most love is coming to see you. However, large numbers of butterflies are viewed as bad omens. When Taira no Masakado was secretly preparing for his famous revolt, there appeared in Kyoto so vast a swarm of butterflies that the people were frightened — -thinking the apparition to be a portent of coming evil.[44]

The Russian word for butterflies, pronounced "bah' bch ka", it also means "bow tie". It is a diminutive of "baba" or "babka" (= "woman, grandmother, cake", whence also "babushka" = "grandmother" in English, "babushka" = "a grandma-style headkerchief") and in Greek it means soul.[45] According to Mircea Eliade's Encyclopedia of Religion, some of the Nagas of Manipur trace their ancestry from a butterfly.[46]

In Chinese culture two butterflies flying together are a symbol of love. Also a famous Chinese folk story called Butterfly Lovers. The Taoist philosopher Zhuangzi once had a dream of being a butterfly flying without care about humanity, however when he woke up and realised it was just a dream, he thought to himself "Was I before a man who dreamt about being a butterfly, or am I now a butterfly who dreams about being a man?"

In some old cultures, butterflies also symbolize rebirth into a new life after being inside a cocoon for a period of time.

Some people say that when a butterfly lands on you it means good luck. The idiom "butterflies in the stomach" is used to describe a state of nervousness.

Technological inspirationEdit

Studies on the reflection of light by the scales on wings of swallowtail butterflies have to led to the innovation of more efficient light-emitting diodes.[47]

The structural colouration of butterflies is inspiring nanotechnology research to produce paints that do not use toxic pigments and in the development of new display technologies.[48]

GalleryEdit

Family Papilionidae- The Swallowtails

Family Pieridae - The Whites and Yellows

Family Riodinidae - The Metalmarks, Punches and Judies

Family Nymphalidae - The Brush-footed Butterflies

Family Lycaenidae - The Blues

Family Hesperiidae - The Skippers

See alsoEdit


Cited referencesEdit

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  26. Article on San Diego Zoo website
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  35. Urquhart, F. A. & N. R. Urquhart. 1977. Overwintering areas and migratory routes of the Monarch butterfly (Danaus p. plexippus, Lepidoptera: Danaidae) in North America, with special reference to the western population. Can. Ent. 109: 1583-1589
  36. Wassenaar L.I., Hobson K.A. 1998. Natal origins of migratory monarch butterflies at wintering colonies in Mexico: new isotopic evidence. Proc Natl Acad Sci U S A. 95(26):15436-9. Full text
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  39. Dennis, R L H, Tim G. Shreeve, Henry R. Arnold and David B. Roy (2005) Does diet breadth control herbivorous insect distribution size? Life history and resource outlets for specialist butterflies. Journal of Insect Conservation 9(3):187-200
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  42. William E. Cooper, Jr. (1998) Conditions favoring anticipatory and reactive displays deflecting predatory attack. Behavioral Ecology 9(6):598-604
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  44. Hearn, Lafcadio (1904). Kwaidan: Stories and Studies of Strange Thing, Dover Publications, Inc.. ISBN 0-486-21901-1.
  45. Hutchins, M., Arthur V. Evans, Rosser W. Garrison and Neil Schlager (Eds) (2003) Grzimek's Animal Life Encyclopedia, 2nd edition. Volume 3, Insects, Farmington Hills, MI: Gale Group, 2003.
  46. Rabuzzi, M. 1997. Butterfly etymology. Cultural Entomology November 1997 Fourth issue online
  47. Vukusic, Pete and Ian Hooper. 2005. Directionally Controlled Fluorescence Emission in Butterflies Science. 310(5751):1151 DOI: 10.1126/science.1116612
  48. Biomimetics at Qualcomm

Other referencesEdit

BooksEdit

  • Boggs, C., Watt, W., Ehrlich, P. 2003. Butterflies: Evolution and Ecology Taking Flight. University of Chicago Press, Chicago, USA.
  • Heppner, J. B. 1998. Classification of Lepidoptera. Holarctic Lepidoptera, Suppl. 1.
  • Pyle, R. M. 1992. Handbook for Butterfly Watchers. Houghton Mifflin. First published, 1984. ISBN 0-395-61629-8

PapersEdit

  • Bergstrom, J., & Wiklund, C. (2005). No Effect of Male Courtship Intensity on Female Remating in the Butterfly Pieris napi: Journal of Insect Behavior Vol 18(4) Jul 2005, 479-489.
  • Brunzel, S. (2002). Experimental density-related emigration in the cranberry fritillary boloria aquilonaris: Journal of Insect Behavior Vol 15(6) Nov 2002, 739-750.
  • Chaves, G. W., Patto, C. E. G., & Benson, W. W. (2006). Complex Non-Aerial Contests in the Lekking Butterfly Charis cadytis (Riodinidae): Journal of Insect Behavior Vol 19(2) Mar 2006, 179-196.
  • Daniels, J. C. (2007). Courtship solicitation by females of the barred sulphur butterfly (Eurema daira) (Lepidoptera: Pieridae): Journal of Insect Behavior Vol 20(1) Jan 2007, 129-135.
  • Darwin, C. (1880). Insects, continued--Order Lepidoptera. New York, NY: D Appleton & Company.
  • Dennis, R. L. H., & Sparks, T. H. (2005). Landscape Resources for the Territorial Nymphalid Butterfly Inachis io: Microsite Landform Selection and Behavioral Responses to Environmental Conditions: Journal of Insect Behavior Vol 18(5) Sep 2005, 725-742.
  • Dolley, W. L., Jr. (1920). The Relative Stimulating Efficiency of Continuous and Intermittent Light in Vanessa Antiopa: Psychobiology Vol 2(2) Apr 1920, 137-176.
  • Fatouros, N. E., Huigens, M. E., van Loon, J. J. A., Dicke, M., & Hilker, M. (2005). Butterfly anti-aphrodisiac lures parasitic wasps: Nature Vol 433(7027) Feb 2005, 704.
  • Ferkau, C., & Fischer, K. (2006). Costs of Reproduction in Male Bicyclus anynana and Pieris napi Butterflies: Effects of Mating History and Food Limitation: Ethology Vol 112(11) Nov 2006, 1117-1127.
  • Fischer, K. (2006). Reduced mating vigor in selection lines of the butterfly Bicyclus anynana: Journal of Insect Behavior Vol 19(5) Sep 2006, 657-668.
  • Frankino, W. A., Zwaan, B. J., Stern, D. L., & Brakefield, P. M. (2005). Natural Selection and Developmental Constraints in the Evolution of Allometries: Science Vol 307(5710) Feb 2005, 718-720.
  • Frentiu, F. D., Bernard, G. D., Cuevas, C. I., Sison-Mangus, M. P., Prudic, K. L., & Briscoe, A. D. (2007). Adaptive evolution of color vision as seen through the eyes of butterflies: PNAS Proceedings of the National Academy of Sciences of the United States of America Vol 104(Suppl1) May 2007, 8634-8640.
  • Friberg, M., & Wiklund, C. (2007). Generation-dependent female choice: Behavioral polyphenism in a bivoltine butterfly: Behavioral Ecology Vol 18(4) Jul-Aug 2007, 758-763.
  • Froy, O., Gotter, A. L., Casselman, A. L., & Reppert, S. M. (2003). Illuminating the circadian clock in monarch butterfly migration: Science Vol 300(5623) May 2003, 1303-1305.
  • Geister, T. L., & Fischer, K. (2007). Testing the beneficial acclimation hypothesis: Temperature effects on mating success in a butterfly: Behavioral Ecology Vol 18(4) Jul-Aug 2007, 658-664.
  • Goulson, D. (2004). Review of Butterflies: Ecology and Evolution Taking Flight: Animal Behaviour Vol 68(3) Sep 2004, 645-645.
  • Hardy, P. B., & Dennis, R. L. H. (2007). Seasonal and daily shifts in substrate use by settling butterflies: Conserving resources for invertebrates has a behavioral dimension: Journal of Insect Behavior Vol 20(2) Mar 2007, 181-199.
  • Hargitt, C. W. (1915). Observations on the behavior of butterflies: Journal of Animal Behavior Vol 5(3) May-Jun 1915, 250-257.
  • Hay-Roe, M. M., & Mankin, R. W. (2004). Wing-Click Sounds of Heliconius cydno alithea (Nymphalidae: Heliconiinae) Butterflies: Journal of Insect Behavior Vol 17(3) May 2004, 329-335.
  • Hegedus, R., & Horvath, G. (2004). Polarizational colours could help polarization-dependent colour vision systems to discriminate between shiny and matt surfaces, but cannot unambiguously code surface orientation: Vision Research Vol 44(20) Sep 2004, 2337-2348.
  • Heinz, C. A., & Feeny, P. (2005). Effects of contact chemistry and host plant experience in the oviposition behaviour of the eastern black swallowtail butterfly: Animal Behaviour Vol 69(1) Jan 2005, 107-115.
  • Janz, N. (2005). The relationship between habitat selection and preference for adult and larval food resources in the polyphagous butterfly Vanessa cardui (Lepidoptera: Nymphalidae): Journal of Insect Behavior Vol 18(6) Nov 2005, 767-780.
  • Joron, M., & Brakefield, P. M. (2003). Captivity masks inbreeding effects on male mating success in butterflies: Nature Vol 424(6945) Jul 2003, 191-194.
  • Kassarov, L. (2003). Are Birds the Primary Selective Force Leading to Evolution of Mimicry and Aposematism in Butterflies? An Opposing Point of View: Behaviour Vol 140(4) Apr 2003, 433-451.
  • Kemp, D. J. (2002). Butterfly contests and flight physiology: Why do older males fight harder? : Behavioral Ecology Vol 13(4) Aug 2002, 456-461.
  • Kemp, D. J. (2003). Twilight fighting in the evening brown butterfly, Melanitis leda (L.) (Nymphalidae): Age and residency effects: Behavioral Ecology and Sociobiology Vol 54(1) Jun 2003, 7-13.
  • Kemp, D. J. (2006). Ultraviolet ornamentation and male mating success in a high-density assemblage of the butterfly Colias eurytheme: Journal of Insect Behavior Vol 19(5) Sep 2006, 669-684.
  • Kemp, D. J. (2008). Female mating biases for bright ultraviolet iridescence in the butterfly Eurema hecabe (Pieridae): Behavioral Ecology Vol 19(1) Jan-Feb 2008, 1-8.
  • Kemp, D. J., & Macedonia, J. M. (2007). Male mating bias and its potential reproductive consequence in the butterfly Colias eurytheme: Behavioral Ecology and Sociobiology Vol 61(3) Jan 2007, 415-422.
  • Kemp, D. J., Wiklund, C., & Gotthard, K. (2006). Life History Effects Upon Contest Behaviour: Age as a Predictor of Territorial Contest Dynamics in Two Populations of the Speckled Wood Butterfly, Pararge aegeria L: Ethology Vol 112(5) May 2006, 471-477.
  • Kemp, D. J., Wiklund, C., & Van Dyck, H. (2006). Contest behaviour in the speckled wood butterfly (Pararge aegeria): Seasonal phenotypic plasticity and the functional significance of flight performance: Behavioral Ecology and Sociobiology Vol 59(3) Jan 2006, 403-411.
  • Knopp, M. C. N., & Krenn, H. W. (2003). Efficiency of Fruit Juice Feeding in Morpho peleides (Nymphalidae, Lepidoptera): Journal of Insect Behavior Vol 16(1) Jan 2003, 67-77.
  • Kronforst, M. R., Young, L. G., Kapan, D. D., McNeely, C., O'Neill, R. J., Gilbert, L. E., et al. (2006). Linkage of butterfly mate preference and wing color preference cue at the genomic location of wingless: PNAS Proceedings of the National Academy of Sciences of the United States of America Vol 103(17) Apr 2006, 6575-6580.
  • Langham, G. M. (2006). Rufous-tailed jacamars and aposematic butterflies: Do older birds attack novel prey? : Behavioral Ecology Vol 17(2) Mar-Apr 2006, 285-290.
  • Lauwers, K., & Van Dyck, H. (2006). The cost of mating with a non-virgin male in a monandrous butterfly: Experimental evidence from the speckled wood, Pararge aegeria: Behavioral Ecology and Sociobiology Vol 60(1) May 2006, 69-76.
  • Lewis, Z., & Wedell, N. (2007). Effect of adult feeding on male mating behaviour in the butterfly, Bicyclus anynana (Lepidoptera: Nymphalidae): Journal of Insect Behavior Vol 20(2) Mar 2007, 201-213.
  • Merckx, T., & van Dyck, H. (2005). Mate location behaviour of the butterfly Pararge aegeria in woodland and fragmented landscapes: Animal Behaviour Vol 70(2) Aug 2005, 411-416.
  • Merckx, T., & Van Dyck, H. (2007). Habitat fragmentation affects habitat-finding ability of the speckled wood butterfly, Pararge aegeria L: Animal Behaviour Vol 74(4) Oct 2007, 1029-1037.
  • Mevi-Schutz, J., Goverde, M., & Erhardt, A. (2003). Effects of fertilization and elevated CO-sub-2 on larval food and butterfly nectar amino acid preference in Coenonympha pamphilus L: Behavioral Ecology and Sociobiology Vol 54(1) Jun 2003, 36-43.
  • Molleman, F., Zwaan, B. J., & Brakefield, P. M. (2004). The effect of male sodium diet and mating history on female reproduction in the puddling squinting bush brown Bicyclus anynana (Lepidoptera): Behavioral Ecology and Sociobiology Vol 56(4) Aug 2004, 404-411.
  • Musche, M., Anton, C., Worgan, A., & Settele, J. (2006). No experimental evidence for host ant related oviposition in a parasitic butterfly: Journal of Insect Behavior Vol 19(5) Sep 2006, 631-643.
  • Otis, G. W., Locke, B., McKenzie, N. G., Cheung, D., Macleod, E., Careless, P., et al. (2006). Local enhancement in mud-puddling swallowtail butterflies (Battus philenor and Papilio glaucus): Journal of Insect Behavior Vol 19(6) Nov 2006, 685-698.
  • Papke, R. S., Kemp, D. J., & Rutowski, R. L. (2007). Multimodal signalling: Structural ultraviolet reflectance predicts male mating success better than pheromones in the butterfly Colias eurytheme L. (Pieridae): Animal Behaviour Vol 73(1) Jan 2007, 47-54.
  • Papke, R. S., Kemp, D. J., & Rutowski, R. L. (2007). "Multimodal signalling: Structural ultraviolet reflectance predicts male mating success better than pheromones in the butterfly Colias eurytheme L. (Pieridae)": Erratum: Animal Behaviour Vol 73(6) Jun 2007, 1083.
  • Pe'er, G., Saltz, D., Hans-Hermann, T., & Motro, U. (2004). Response to topography in a hilltopping butterfly and implications for modelling nonrandom dispersal: Animal Behaviour Vol 68(4) Oct 2004, 825-839.
  • Peterson, R. K. D., Meyer, S. J., Wolf, A. T., Wolt, J. D., & Davis, P. M. (2006). Genetically Engineered Plants, Endangered Species, and Risk: A Temporal and Spatial Exposure Assessment for Karner Blue Butterfly Larvae and Bt Maize Pollen: Risk Analysis Vol 26(3) Jun 2006, 845-858.
  • Rau, P. (1917). The courtship of Pieris protodice: Journal of Animal Behavior Vol 7(2) Mar-Apr 1917, 143-144.
  • Rensch, B. (1965). The leaf-rolling activity of caterpillars of certain Indo-Australian butterflies: Zeitschrift fur Tierpsychologie 22(1) 1965, 6-14.
  • Rutowski, R. L., McCoy, L., & Demlong, M. J. (2001). Visual mate detection in a territorial male butterfly (Asterocampa leilia): Effects of distance and perch location: Behaviour Vol 138(1) Jan 2001, 31-43.
  • Solensky, M. J. (2004). The Effect of Behavior and Ecology on Male Mating Success in Overwintering Monarch Butterflies (Danaus plexippus): Journal of Insect Behavior Vol 17(6) Nov 2004, 723-743.
  • Spieth, H. R., Xue, F., & Strauss, K. (2004). Induction and Inhibition of Diapause by the Same Photoperiod: Experimental Evidence for a "Double Circadian Oscillator Clock": Journal of Biological Rhythms Vol 19(6) Dec 2004, 483-492.
  • Srygley, R. B., Dudley, R., Oliveira, E. G., & Riveros, A. J. (2006). Experimental evidence for a magnetic sense in neotropical migrating butterflies (Lepidoptera: Piendae): Animal Behaviour Vol 71(1) Jan 2006, 183-191.
  • Sweeney, A., Jiggins, C., & Johnsen, S. (2003). Polarized light as a butterfly mating signal: Nature Vol 423(6935) May 2003, 31-32.
  • Takeuchi, T. (2006). The effect of morphology and physiology on butterfly territoriality: Behaviour Vol 143(3) Mar 2006, 393-403.
  • Takeuchi, T. (2006). Matter of Size or Matter of Residency Experience? Territorial Contest in a Green Hairstreak, Chrysozephyrus smaragdinus (Lepidoptera: Lycaenidae): Ethology Vol 112(3) Mar 2006, 293-299.
  • Valimaki, P., Kaitala, A., & Kokko, H. (2006). Temporal patterns in reproduction may explain variation in mating frequencies in the green-veined white butterfly Pieris napi: Behavioral Ecology and Sociobiology Vol 61(1) Nov 2006, 99-107.
  • Vallin, A., Jakobsson, S., Lind, J., & Wiklund, C. (2006). Crypsis versus intimidation-anti-predation defence in three closely related butterflies: Behavioral Ecology and Sociobiology Vol 59(3) Jan 2006, 455-459.
  • Vallin, A., Jakobsson, S., & Wiklund, C. (2007). "An eye for an eye?"--On the generality of the intimidating quality of eyespots in a butterfly and a hawkmoth: Behavioral Ecology and Sociobiology Vol 61(9) Jul 2007, 1419-1424.
  • Wedell, N., Wiklund, C., & Cook, P. A. (2002). Monandry and polyandry as alternative lifestyles in a butterfly: Behavioral Ecology Vol 13(4) Aug 2002, 450-455.
  • Weiss, M. R., & Papaj, D. R. (2003). Colour learning in two behavioural contexts: How much can a butterfly keep in mind? : Animal Behaviour Vol 65(3) Mar 2003, 425-434.
  • Wiklund, C., & Tullberg, B. (2004). Seasonal polyphenism and leaf mimicry in the comma butterfly: Animal Behaviour Vol 68(3) Sep 2004, 621-627.



Field guides to butterfliesEdit

File:Lepidoptera 001.jpg
  • Butterflies of North America, Jim P. Brock and Kenn Kaufman (2003)
  • Butterflies through Binoculars: The East, Jeffrey Glassberg (1999)
  • Butterflies through Binoculars: The West, Jeffrey Glassberg (2001)
  • A Field Guide to Eastern Butterflies, Paul Opler (1994)
  • A Field Guide to Western Butterflies, Paul Opler (1999)
  • Peterson First Guide to Butterflies and Moths, Paul Opler (1994)
  • Las Mariposas de Machu Picchu by Gerardo Lamas (2003)
  • The Millennium Atlas of Butterflies in Britain and Ireland by Jim Asher (Editor), et al.
  • Pocket Guide to the Butterflies of Great Britain and Ireland by Richard Lewington
  • Butterflies of Britain and Europe (Collins Wildlife Trust Guides) by Michael Chinery
  • Butterflies of Europe by Tom Tolman and Richard Lewington (2001)
  • Butterflies of Europe New Field Guide and Key by Tristan Lafranchis (2004)
  • Field Guide to Butterlies of South Africa by Steve Woodhall (2005)
  • Butterflies of Sikkim Himalaya and their Natural History by Meena Haribal (1994).
  • Butterflies of Peninsular India by Krushnamegh Kunte, Universities Press (2005).
  • Butterflies of the Indian Region by Col M. A. Wynter-Blyth, Bombay Natural History Society, Mumbai, India (1957).
  • A Guide to Common Butterflies of Singapore by Steven Neo Say Hian (Singapore Science Centre)
  • Butterflies of West Malaysia and Singapore by W.A.Fleming. (Longman Malaysia)
  • The Butterflies of the Malay Peninsula by A.S. Corbet and H. M. Pendlebury. (The Malayan Nature Society)

External linksEdit

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