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Friday, March 6, 2015

Lepidoptera (butterflies and moths)

From Wikipedia, the free encyclopedia

Lepidoptera
Temporal range: Early Jurassic-Recent, 190–0Ma
Danaus plexippus & Actias luna.jpg
Monarch butterfly and Luna moth, two widely recognized lepidopterans
Scientific classification e
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Superorder: Panorpida
(unranked): Amphiesmenoptera
Order: Lepidoptera
Linnaeus, 1758
Suborders
Aglossata
Glossata
Heterobathmiina
Zeugloptera

The Lepidoptera (/ˌlɛpɨˈdɒptərə/ lep-i-DOP-tər-ə) is an order of insects that includes moths and butterflies (both called lepidopterans). 180,000 species of Lepidoptera are described, in 126 families[1] and 46 superfamilies,[2] 10% of the total described species of living organisms.[2][3] It is one of the most widespread and widely recognizable insect orders in the world,[4] encompassing moths and the three superfamilies of butterflies, skipper butterflies, and moth-butterflies. The term was coined by Linnaeus in 1735 and is derived from Ancient Greek λεπίδος (scale) and πτερόν (wing).[5] the Lepidoptera show many variations of the basic body structure that have evolved to gain advantages in lifestyle and distribution. Recent estimates suggest the order may have more species than earlier thought,[6] and is among the four most speciose orders, along with the Hymenoptera, Diptera, and Coleoptera.[4]

Lepidopteran species are characterized by more than three derived features, some of the most apparent being the scales covering their bodies and wings, and a proboscis. The scales are modified, flattened "hairs", and give butterflies and moths their extraordinary variety of colors and patterns. Almost all species have some form of membranous wings, except for a few that have reduced wings or are wingless. Like most other insects, butterflies and moths are holometabolous, meaning they undergo complete metamorphosis. Mating and the laying of eggs are carried out by adults, normally near or on host plants for the larvae. The larvae are commonly called caterpillars, and are completely different from their adult moth or butterfly forms, having a cylindrical body with a well-developed head, mandible mouth parts, and from none to 11 (usually eight) pairs of prolegs. As they grow, these larvae change in appearance, going through a series of stages called instars. Once fully matured, the larva develops into a pupa, referred to as a chrysalis in the case of butterflies and a cocoon in the case of moths. A few butterflies and many moth species spin a silk case or cocoon prior to pupating, while others do not, instead going underground.[4]

The Lepidoptera have, over millions of years, evolved a wide range of wing patterns and coloration ranging from drab moths akin to the related order Trichoptera, to the brightly colored and complex-patterned butterflies.[1] Accordingly, this is the most recognized and popular of insect orders with many people involved in the observation, study, collection, rearing of, and commerce in these insects. A person who collects or studies this order is referred to as a lepidopterist.

Butterflies and moths play an important role in the natural ecosystem as pollinators and as food in the food chain; conversely, their larvae are considered very problematic to vegetation in agriculture, as their main source of food is often live plant matter. In many species, the female may produce from 200 to 600 eggs, while in others, the number may approach 30,000 eggs in one day. The caterpillars hatching from these eggs can cause damage to large quantities of crops. Many moth and butterfly species are of economic interest by virtue of their role as pollinators, the silk they produce, or as pest species.

Etymology

The word Lepidoptera comes from the Latin word for "scaly wing", from the Ancient Greek λεπίς (lepis) meaning scale and πτερόν (pteron) meaning wing.[5] Sometimes, the term Rhopalocera is used to group the species that are butterflies, derived from the Ancient Greek ῥόπαλον (rhopalon)[7]:4150 and κέρας (kæras)[7]:3993 meaning "club" and "horn", respectively, coming from the shape of the antennae of butterflies.

The origins of the common names "butterfly" and "moth" are varied and often obscure. The English word butterfly is from Old English buttorfleoge, with many variations in spelling. Other than that, the origin is unknown, although it could be derived from the pale yellow color of many species' wings suggesting the color of butter.[8][9] The species of Heterocera are commonly called moths. The origins of the English word moth are more clear, deriving from the Old English moððe" (cf. Northumbrian dialect mohðe) from Common Germanic (compare Old Norse motti, Dutch mot and German Motte all meaning "moth"). Perhaps its origins are related to Old English maða meaning "maggot" or from the root of "midge", which until the 16th century was used mostly to indicate the larva, usually in reference to devouring clothes.[10]

The etymological origins of the word "caterpillar", the larval form of butterflies and moths, are from the early 16th century, from Middle English catirpel, catirpeller, probably an alteration of Old North French catepelose: cate, cat (from Latin cattus) + pelose, hairy (from Latin pilōsus).[11]

Distribution and diversity

The Lepidoptera are among the most successful groups of insects. They are found on all continents, except Antarctica, and inhabit all terrestrial habitats ranging from desert to rainforest, from lowland grasslands to montane plateaus, but almost always associated with higher plants, especially angiosperms (flowering plants).[12] Among the most northern dwelling species of butterflies and moths is the Arctic Apollo (Parnassius arcticus), which is found in the Arctic Circle in northeastern Yakutia, at an altitude of 1500 meters above sea level.[13] In the Himalayas, various Apollo species such as Parnassius epaphus, besides others, have been recorded to occur up to an altitude of 6,000 m above sea level.[14]:221
Some lepidopteran species exhibit symbiotic, phoretic, or parasitic lifestyles, inhabiting the bodies of organisms rather than the environment. Coprophagous pyralid moth species, called sloth moths, such as Bradipodicola hahneli and Cryptoses choloepi, are unusual in that they are exclusively found inhabiting the fur of sloths, mammals found in Central and South America.[15][16] Two species of Tinea moths have been recorded as feeding on horny tissue and have been bred from the horns of cattle. The larva of Zenodochium coccivorella is an internal parasite of the coccid Kermes species. Many species have been recorded as breeding in natural materials or refuse such as owl pellets, bat caves, honeycombs or diseased fruit.[16]

Of the roughly 174,250 lepidopteran species described until 2007, butterflies and skippers are estimated to comprise around 17,950, with moths making up the rest.[2][17] The vast majority of Lepidoptera are to be found in the tropics, but substantial diversity exists on most continents. North America has over 700 species of butterflies and over 11,000 species of moths,[18][19] while about 400 species of butterflies and 14,000 species of moths are reported from Australia.[20] The diversity of Lepidoptera in each faunal region has been estimated by John Heppner in 1991 based partly on actual counts from the literature, partly on the card indices in the Natural History Museum (London) and the National Museum of Natural History (Washington), and partly on estimates:[6]

Diversity of Lepidoptera in each faunal region
Palearctic Nearctic Neotropic Afrotropic Indo-Australian
(comprising Indomalayan and Australian regions)
Estimated number of species 22,465 11,532 44,791 20,491 47,286

External morphology

Parts of an adult butterfly

A – head, B – thorax, C – abdomen, 1 – prothoracic shield, 2 – spiracle, 3 – true legs, 4 – midabdominal prolegs, 5 – anal proleg, 6 – anal plate, 7 – tentacle, a – frontal triangle, b – stemmata (ocelli), c – antenna, d – mandible, e – labrum.

Lepidoptera are morphologically distinguished from other orders principally by the presence of scales on the external parts of the body and appendages, especially the wings. Butterflies and moths vary in size from microlepidoptera only a few millimeters long, to conspicuous animals with a wingspan of many inches, such as the Monarch butterfly and Atlas moth.[21]:246 Lepidopterans undergo a four-stage lifecycle: egg; larva or caterpillar; pupa or chrysalis; and imago (plural: imagines) / adult and show many variations of the basic body structure, which have evolved to gain advantages in lifestyle and distribution.

Head


The face of a caterpillar with the mouthparts showing

The head is where many sensing organs and the mouth parts are found. Like the adult, the larva also has a toughened, or sclerotized head capsule.[22] Here, two compound eyes, and chaetosema, raised spots or clusters of sensory bristles unique to Lepidoptera, occur, though many taxa have lost one or both of these spots. The antennae have a wide variation in form among species and even between different sexes. The antennae of butterflies are usually filiform and shaped like clubs, those of the skippers are hooked, while those of moths have flagellar segments variously enlarged or branched. Some moths have enlarged antennae, or they are tapered and hooked at the ends.[23]:559–560

The maxillary galeae are modified and form an elongated proboscis. The proboscis consists of one to five segments, usually kept coiled up under the head by small muscles when it is not being used to suck up nectar from flowers or other liquids. Some basal moths still have mandibles, or separate moving jaws, like their ancestors and these form the family Micropterigidae.[22][23]:560[24]

The larvae, called caterpillars, have a toughened head capsule. Caterpillars lack the proboscis and have separate chewing mouthparts.[22] These mouthparts, called mandibles, are used to chew up the plant matter that the larvae eat. The lower jaw, or labium, is weak, but may carry a spinneret, an organ used to create silk. The head is made of large lateral lobes, each having an ellipse of up to six simple eyes.[23]:562–563

Thorax

The thorax is made of three fused segments, the prothorax, mesothorax, and metathorax, each with a pair of legs. The first segment contains the first pair of legs. In some males of the butterfly family Nymphalidae, the fore legs are greatly reduced and are not used for walking or perching.[23]:586 The three pairs of legs are covered with scales. Lepidoptera also have olfactory organs on their feet, which aid the butterfly in "tasting" or "smelling" out its food.[25] In the larval form there are 3 pairs of true legs, with up to 11 pairs of abdominal legs (usually eight) and hooklets, called apical crochets.[12]

The two pairs of wings are found on the middle and third segments, or mesothorax and metathorax, respectively. In the more recent genera, the wings of the second segment are much more pronounced, although some more primitive forms have similarly sized wings of both segments. The wings are covered in scales arranged like shingles, which form an extraordinary variety of colors and patterns. The mesothorax is designed to have more powerful muscles to propel the moth or butterfly through the air, with the wing of this segment (fore wing) having a stronger vein structure.[23]:560 The largest superfamily, the Noctuidae, has their wings modified to act as tympanal or hearing organs.[26]

The caterpillar has an elongated, soft body that may have hair-like or other projections, three pairs of true legs, with none to 11 pairs of abdominal legs (usually eight) and hooklets, called apical crochets.[12] The thorax usually has a pair of legs on each segment. The thorax is also lined with many spiracles on both the mesothorax and metathorax, except for a few aquatic species, which instead have a form of gills.[23]:563

Abdomen


Caterpillar prolegs on Papilio machaon

The abdomen, which is less sclerotized than the thorax, consists of 10 segments with membranes in between, allowing for articulated movement. The sternum, on the first segment, is small in some families and is completely absent in others. The last two or three segments form the external parts of the species' sex organs. The genitalia of Lepidoptera are highly varied and are often the only means of differentiating between species. Male genitals include a valva, which is usually large, as it is used to grasp the female during mating. Female genitalia include three distinct sections.

The females of basal moths have only one sex organ, which is used for copulation and as an ovipositor, or egg-laying organ. About 98% of moth species have a separate organ for mating, and an external duct that carries the sperm from the male.[23]:561

The abdomen of the caterpillar has four pairs of prolegs, normally located on the third to sixth segments of the abdomen, and a separate pair of prolegs by the anus, which have a pair of tiny hooks called crotchets. These aid in gripping and walking, especially in species that lack many prolegs (e. g. larvae of Geometridae). In some basal moths, these prolegs may be on every segment of the body, while prolegs may be lost completely in other groups, which are more adapted to boring and living in sand (e. g., Prodoxidae and Nepticulidae, respectively).[23]:563

Scales


Wing scales form the color and pattern on wings. The scales shown here are lamellar. The pedicel can be seen attached to a few loose scales.

The wings, head, and parts of the thorax and abdomen of Lepidoptera are covered with minute scales, a feature from which the order derives its name. Most scales are lamellar, or blade-like and attached with a pedicel, while other forms may be hair-like or specialized as secondary sexual characteristics.[27]

The lumen or surface of the lamella has a complex structure. It gives color either by colored pigments it contains, or through structural coloration with mechanisms that include photonic crystals and diffraction gratings.[28]

Scales function in insulation, thermoregulation, producing pheromones (in males only),[29] and aiding gliding flight, but the most important is the large diversity of vivid or indistinct patterns they provide, which help the organism protect itself by camouflage or mimicry, and which act as signals to other animals including rivals and potential mates.[27]

Electron microscopy images of scales
A patch of wing (×50)
Scales close up (×200)
A single scale (×1000)
Microstructure of a scale (×5000)

Internal morphology

In the reproductive system of butterflies and moths, the male genitalia are complex and unclear. In females the three types of genitalia are based on the relating taxa: 'monotrysian', 'exoporian', and 'ditrysian'. In the monotrysian type is an opening on the fused segments of the sterna 9 and 10, which act as insemination and oviposition. In the exoporian type (in Hepaloidae and Mnesarchaeoidea) are two separate places for insemination and oviposition, both occurring on the same sterna as the monotrysian type, i.e. 9 and 10.[21] The ditrysian groups have an internal duct that carries sperm, with separate openings for copulation and egg-laying.[4] In most species, the genitalia are flanked by two soft lobes, although they may be specialized and sclerotized in some species for ovipositing in area such as crevices and inside plant tissue.[21] Hormones and the glands that produce them run the development of butterflies and moths as they go through their lifecycles, called the endocrine system. The first insect hormone prothoracicotropic hormone(PTTH) operates the species lifecycle and diapause.[30] This hormone is produced by corpora allata and corpora cardiaca, where it is also stored. Some glands are specialized to perform certain task such as producing silk or producing saliva in the palpi.[31]:65, 75 While the corpora cardiaca produce PTTH, the corpora allata also produces juvenile hormones, and the prothorocic glands produce moulting hormones.

In the digestive system, the anterior region of the foregut has been modified to form a pharyngeal sucking pump as they need it for the food they eat, which are for the most part liquids. An esophagus follows and leads to the posterior of the pharynx and in some species forms a form of crop. The midgut is short and straight, with the hindgut being longer and coiled.[21] Ancestors of lepidopteran species, stemming from Hymenoptera, had midgut ceca, although this is lost in current butterflies and moths. Instead, all the digestive enzymes, other than initial digestion, are immobilized at the surface of the midgut cells. In larvae, long-necked and stalked goblet cells are found in the anterior and posterior midgut regions, respectively. In insects, the goblet cells excrete positive potassium ions, which are absorbed from leaves ingested by the larvae. Most butterflies and moths display the usual digestive cycle, but species with different diets require adaptations to meet these new demands.[23]:279

Internal morphology of adult male in the family Nymphalidae, showing most of the major organ systems, with characteristic reduced forelegs of that family: The corpora include the corpus allatum and the corpus cardiaca.

In the circulatory system, hemolymph, or insect blood, is used to circulate heat in a form of thermoregulation, where muscles contraction produces heat, which is transferred to the rest of the body when conditions are unfavorable.[32] In lepidopteran species, hemolymph is circulated through the veins in the wings by some form of pulsating organ, either by the heart or by the intake of air into the trachea.[31]:69 Air is taken in through spiracles along the sides of the abdomen and thorax supplying the trachea with oxygen as it goes through the lepidopteran's respiratory system. Thee different tracheae supply and diffuse oxygen throughout the species' bodies. The dorsal tracheae supply oxygen to the dorsal musculature and vessels, while the ventral tracheae supply the ventral musculature and nerve cord, and the visceral tracheae supply the guts, fat bodies, and gonads.[31]:71, 72

Polymorphism

Sexually dimorphic bagworm moths (Thyridopteryx ephemeraeformis) mating: The female is flightless.

The Heliconius butterflies from the tropics of the Western Hemisphere are the classical model for Müllerian mimicry.

Polymorphism is the appearance of forms or "morphs", which differ in color and number of attributes within a single species.[12]:163[33] In Lepidoptera, polymorphism can be seen not only between individuals in a population, but also between the sexes as sexual dimorphism, between geographically separated populations in geographical polymorphism, and between generations flying at different seasons of the year (seasonal polymorphism or polyphenism). In some species, the polymorphism is limited to one sex, typically the female. This often includes the phenomenon of mimicry when mimetic morphs fly alongside nonmimetic morphs in a population of a particular species. Polymorphism occurs both at specific level with heritable variation in the overall morphological design of individuals, as well as in certain specific morphological or physiological traits within a species.[12]

Environmental polymorphism, in which traits are not inherited, is often termed as polyphenism, which in Lepidoptera is commonly seen in the form of seasonal morphs, especially in the butterfly families of Nymphalidae and Pieridae. An Old World pierid butterfly, the common grass yellow (Eurema hecabe) has a darker summer adult morph, triggered by a long day exceeding 13 hours in duration, while the shorter diurnal period of 12 hours or less induces a paler morph in the postmonsoon period.[34] Polyphenism also occurs in caterpillars, an example being the peppered moth, Biston betularia.[35]

Geographical isolation causes a divergence of a species into different morphs. A good example is the Indian white admiral Limenitis procris, which has five forms, each geographically separated from the other by large mountain ranges.[36]:26 An even more dramatic showcase of geographical polymorphism is the Apollo butterfly (Parnassius apollo). Because the Apollos live in small local populations, thus having no contact with each other, coupled with their strong stenotopic nature and weak migration ability, interbreeding between populations of one species practically does not occur; by this, they form over 600 different morphs, with the size of spots on the wings of which varies greatly.[37]

Seasonal diphenism in the common grass yellow, Eurema hecabe
Dry-season form
Wet-season form

Sexual dimorphism is the occurrence of differences between males and females in a species. In Lepidoptera, it is widespread and almost completely set by genetic determination.[34] Sexual dimorphism is present in all families of the Papilionoidea and more prominent in the Lycaenidae, Pieridae, and certain taxa of the Nymphalidae. Apart from color variation, which may differ from slight to completely different color-pattern combinations, secondary sexual characteristics may also be present.[36]:25 Different genotypes maintained by natural selection may also be expressed at the same time.[34] Polymorphic and/or mimetic females occur in the case of some taxa in the Papilionidae primarily to obtain a level of protection not available to the male of their species. The most distinct case of sexual dimorphism is that of adult females of many Psychidae species which have only vestigial wings, legs, and mouthparts as compared to the adult males that are strong fliers with well-developed wings and feathery antennae.[38]

Reproduction and development


Mating pair of Laothoe populi (poplar hawk-moth) showing two different color variants

Species of Lepidoptera undergo holometabolism or "complete metamorphosis". Their lifecycle normally consists of an egg, a larva, a pupa, and an imago or adult.[12] The larvae are commonly called caterpillars, and the pupae of moths encapsulated in silk are called cocoons, while the uncovered pupae of butterflies are called chrysalides.

Mating

Males usually start eclosion (emergence) earlier than females and peak in numbers before females. Both of the sexes are sexually mature by the time of eclosion.[23]:564 Butterflies and moths normally do not associate with each other, except for migrating species, staying relatively asocial. Mating begins with an adult (female or male) attracting a mate, normally using visual stimuli, especially in diurnal species like most butterflies. However, the females of most nocturnal species, including almost all moth species, use pheromones to attract males, sometimes from long distances.[12] Some species engage in a form of acoustic courtship, or attract mates using sound or vibration such as the polka-dot wasp moth, Syntomeida epilais.[39]
Adaptations include undergoing one seasonal generation, two or even more, called voltinism (Univoltism, bivoltism, and multivism, respectively). Most lepidopterans in temperate climates are univoltine, while in tropical climates most have two seasonal broods. Some others may take advantage of any opportunity they can get, and mate continuously throughout the year. These seasonal adaptations are controlled by hormones, and these delays in reproduction are called diapause.[23]:567 Many lepidopteran species, after mating and laying their eggs, die shortly afterwards, having only lived for a few days after eclosion. Others may still be active for several weeks and then overwinter and become sexually active again when the weather becomes more favorable, or diapause. The sperm of the male that mated most recently with the female is most likely to have fertilized the eggs, but the sperm from a prior mating may still prevail.[23]:564

Lifecycle


The four stages of the lifecycle of an anise swallowtail

Eggs

Lepidoptera usually reproduce sexually and are oviparous (egg-laying), though some species exhibit live birth in a process called ovoviviparity. A variety of differences in egg-laying and the number of eggs laid occur. Some species simply drop their eggs in flight (these species normally have polyphagous larvae, meaning they eat a variety of plants e. g., hepialids and some nymphalids)[40] while most lay their eggs near or on the host plant on which the larvae fee. The number of eggs laid may vary from only a few to several thousand.[12] The females of both butterflies and moths select the host plant instinctively, and primarily, by chemical cues.[23]:564

The egg is covered by a hard-ridged protective outer layer of shell, called the chorion. It 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 micropyles, or tiny funnel-shaped openings at one end, the purpose of which 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.

The egg stage lasts a few weeks in most butterflies, but eggs laid close to winter, especially in temperate regions, go through a diapause, and hatching may be delayed until spring. Other butterflies may lay their eggs in the spring and have them hatch in the summer. These butterflies are usually northern species (e. g. Nymphalis antiopa).

Larvae


The larval form typically lives and feeds on plants.

The larvae or caterpillars are the first stage in the lifecycle after hatching. Caterpillars, are "characteristic polypod larvae with cylindrical bodies, short thoracic legs, and abdominal prolegs (pseudopods)".[41] They have a toughened (sclerotised) head capsule with an adfrontal suture formed by medial fusion of the sclerites, mandibles (mouthparts) for chewing, and a soft tubular, segmented body, that may have hair-like or other projections, three pairs of true legs, and additional prolegs (up to five pairs).[42] The body consists of thirteen segments, of which three are thoracic and ten are abdominal.[43] Most larvae are herbivores, but a few are carnivores (some eat ants or other caterpillars) and detritivores.[42]

Different herbivorous species have adapted to feed on every part of the plant and are normally considered pests to their host plants; some species have been found to lay their eggs on the fruit and other species lay their eggs on clothing or fur (e. g., Tineola bisselliella, the common clothes moth). Some species are carnivorous and others are even parasitic. Some lycaenid species such as Maculinea rebeli are social parasites of Myrmica ants nests.[44] A species of Geometridae from Hawaii has carnivorous larvae that catch and eat flies.[45] Some pyralid caterpillars are aquatic.[46]

The larvae develop rapidly with several generations in a year; however, some species may take up to 3 years to develop, and exceptional examples like Gynaephora groenlandica take as long as seven years.[12] The larval stage is where the feeding and growing stages occur, and the larvae periodically undergo hormone-induced ecdysis, developing further with each instar, until they undergo the final larval-pupal molt. The lepidopteran pupa, known as a chrysalis in the case of butterflies, has functional mandibles with appendages fused or glued to the body in most species, while the pupal mandibles are not functional in others.[22]

The larvae of both butterflies and moths exhibit mimicry to deter potential predators. Some caterpillars have the ability to inflate parts of their heads to appear snake-like. Many have false eye-spots to enhance this effect. Some caterpillars have special structures called osmeteria (Papilionidae family), which are exposed to produce smelly chemicals 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 make them unpalatable to birds and other predators. Such unpalatability is advertised using bright red, orange, black, or white warning colors. 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.[47]

Wing development

No form of wing is externally visible on the larva, but when larvae are dissected, developing wings can be seen as disks, which 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.[48]

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.[48]

Pupa

Eclosion of Papilio dardanus

After about five to seven instars,[49]:26–28 or molts, certain hormones, like PTTH, stimulate the production of ecdysone, which initiates insect molting. Then, the larva puparium, a sclerotized or hardened cuticle of the last larval instar, develops into the pupa. Depending on the species, the pupa may be covered in silk and attached to many different types of debris, or may not be covered at all. The pupa stays attached to the leaf by silk spun by the caterpillar before it spins the silk for the full pupa.[23]:566 Features of the imago are externally recognizable in the pupa. All the appendages on the adult head and thorax are found cased inside the cuticle (antennae, mouthparts, etc.), with the wings wrapped around, adjacent to the antennae.[23]:564

While encased, some of the lower segments are not fused, and are able to move using small muscles found in between the membrane. Moving may help the pupa, for example, escape the sun, which would otherwise kill it. The pupa of the Mexican jumping bean moth (Cydia deshaisiana) does this. The larvae cut a trapdoor in the bean (species of Sebastiania) and use the bean as a shelter. With a sudden rise in temperature, the pupa inside twitches and jerks, pulling on the threads inside. Wiggling may also help to deter parasitoid wasps from laying eggs on the pupa. Other species of moths are able to make clicks to deter predators.[23]:564, 566

The length of time before the pupa ecloses (emerges) varies greatly. The monarch butterfly may stay in its chrysalis for two weeks, while other species may need to stay for more than 10 months in diapause. The adult emerges from the pupa either by using abdominal hooks or from projections located on the head. The mandibles found in the most primitive moth families are used to escape from their cocoon (e. g., Micropterigoidea).[12][23]:564

Adult

Most lepidopteran species do not live long after eclosion, only needing a few days to find a mate and then lay their eggs. Others may remain active for a longer period (from one to several weeks), or go through diapause and overwintering as monarch butterflies do, or waiting out environmental stress.
Some adult species of Microlepidoptera go through a stage where no reproductive-related activity occurs, lasting through summer and winter, followed by mating and oviposition in the early spring.[23]:564

While most butterflies and moths are terrestrial, many species of Pyralidae are truly aquatic with all stages except the adult occurring in water. Many species from other families such as Arctiidae, Nepticulidae, Cosmopterygidae, Tortricidae, Olethreutidae, Noctuidae, Cossidae, and Sphingidae are aquatic or semiaquatic.[50]:22

Behavior

Flight

Flight is an important aspect of the lives of butterflies and moths, and is used for evading predators, searching for food, and finding mates in a timely manner, as lepidopteran species do not live long after eclosion. It is the main form of locomotion in most species. In Lepidoptera, the fore wings and hind wings are mechanically coupled and flap in synchrony. Flight is anteromotoric, or being driven primarily by action of the fore wings. Although lepidopteran species reportedly can still fly when their hind wings are cut off, it reduces their linear flight and turning capabilities.[51]

Lepidopteran species have to be warm, about 77 to 79 °F (25 to 26 °C), to fly. They depend on their body temperature being sufficiently high and since they cannot regulate it themselves, this is dependent on their environment. Butterflies living in cooler climates may use their wings to warm their bodies. They will bask in the sun, spreading out their wings so that they get maximum exposure to the sunlight. In hotter climates butterflies can easily overheat, so they are usually active only during the cooler parts of the day, early morning, late afternoon or early evening. During the heat of the day, they rest in the shade. Some larger thick-bodied moths (e.g. Sphingidae) can generate their own heat to a limited degree by vibrating their wings. The heat generated by the flight muscles warms the thorax while the temperature of the abdomen is unimportant for flight. To avoid overheating, some moths rely on hairy scales, internal air sacs, and other structures to separate the thorax and abdomen and keep the abdomen cooler.[52]

Some species of butterflies can reach fast speeds, such as the southern dart, which can go as fast as 48.4 km/h. Sphingids are some of the fastest flying insects, some are capable of flying at over 50 km/h (30 mi/h), having a wingspan of 35–150 mm.[1][53] In some species, sometimes a gliding component to their flight exists. Flight occurs either as hovering, or as forward or backward motion.[54] In butterfly and moth species, such as hawk moths, hovering is important as they need to maintain a certain stability over flowers when feeding on the nectar.[1]

Navigation


Timelapse of flying moths, attracted to the floodlights

Navigation is important to lepidoptera species, especially for those that migrate. Butterflies, which have more species that migrate, have been shown to navigate using time-compensated sun compasses. They can see polarized light, so can orient even in cloudy conditions. The polarized light in the region close to the ultraviolet spectrum is suggested to be particularly important.[55] Most migratory butterflies are those that live in semiarid areas where breeding seasons are short.[56] The life histories of their host plants also influence the strategies of the butterflies.[57] Other theories include the use of landscapes. Lepidoptera may use coastal lines, mountains, and even roads to orient themselves. Above sea, the flight direction is much more accurate if the coast is still visible.[58]

Many studies have also shown that moths navigate. One study showed that many moths may use the Earth's magnetic field to navigate, as a study of the moth heart and dart suggests.[59] Another study, of the migratory behavior of the silver Y, showed, even at high altitudes, the species can correct its course with changing winds, and prefers flying with favourable winds, suggesting a great sense of direction.[60][61] Aphrissa statira in Panama loses its navigational capacity when exposed to a magnetic field, suggesting it uses the Earth’s magnetic field.[62]

Moths exhibit a tendency to circle artificial lights repeatedly. This suggests they use a technique of celestial navigation called transverse orientation. By maintaining a constant angular relationship to a bright celestial light, such as the Moon, they can fly in a straight line. Celestial objects are so far away, even after traveling great distances, the change in angle between the moth and the light source is negligible; further, the moon will always be in the upper part of the visual field or on the horizon. When a moth encounters a much closer artificial light and uses it for navigation, the angle changes noticeably after only a short distance, in addition to being often below the horizon. The moth instinctively attempts to correct by turning toward the light, causing airborne moths to come plummeting downwards, and at close range, which results in a spiral flight path that gets closer and closer to the light source.[63] Other explanations have been suggested, such as the idea that moths may be impaired with a visual distortion called a Mach band by Henry Hsiao in 1972. He stated that they fly towards the darkest part of the sky in pursuit of safety, thus are inclined to circle ambient objects in the Mach band region.[64]

Migration

Monarch butterflies, seen in a cluster in Santa Cruz, California, where the western population migrates for the winter

Lepidopteran migration is typically seasonal, as the insects moving to escape dry seasons or other disadvantageous conditions. Most lepidopterans that migrate are butterflies, and the distance travelled varies. Some butterflies that migrate include the mourning cloak, painted lady, American lady, red admiral, and the common buckeye.[49]:29–30 The most well-known migrations are those of the eastern population of the monarch butterfly from Mexico to northern United States and southern Canada, a distance of about 4,000–4,800 km (2,500–3,000 mi). 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.[65] Migrations have been studied in more recent times using wing tags and stable hydrogen isotopes.[66][67]

Moths also undertake migrations, an example being the uraniids. Urania fulgens undergoes population explosions and massive migrations that may be not surpassed by any other insect in the Neotropics. In Costa Rica and Panama, the first population movements may begin in July and early August and depending on the year, may be very massive, continuing unabated for as long as five months.[68]

Communication

Pheromones are commonly involved in mating rituals among species, especially moths, but they are also an important aspect of other forms of communication. Usually, the pheromones are produced by either the male or the female and detected by members of the opposite sex with their antennae.[69] In many species, a gland between the eighth and ninth segments under the abdomen in the female produces the pheromones.[12] Communication can also occur through stridulation, or producing sounds by rubbing various parts of the body together.[61]

Moths are known to engage in acoustic forms of communication, most often as courtship, attracting mates using sound or vibration. Like most other insects, moths pick up these sounds using tympanic membranes in their abdomens.[70] An example is that of the polka-dot wasp moth (Syntomeida epilais), which produces sounds with a frequency above that normally detectable by humans (about 20 kHz). These sounds also function as tactile communication, or communication through touch, as they stridulate, or vibrate a substrate like leaves and stems.[39]

Most moths lack bright colors, as many species use coloration as camouflage, but butterflies engage in visual communication. Female cabbage butterflies, for example, use ultraviolet light to communicate, with scales colored in this range on the dorsal wing surface. When they fly, each down stroke of the wing creates a brief flash of ultraviolet light which the males apparently recognize as the flight signature of a potential mate. These flashes from the wings may attract several males that engage in aerial courtship displays.[70]

Ecology

Moths and butterflies are important in the natural ecosystem. They are integral participants in the food chain; having co-evolved with flowering plants and predators, lepidopteran species have formed a network of trophic relationships between autotrophs and heterotrophs, which are included in the stages of Lepidoptera larvae, pupae, and adults. Larvae and pupae are links in the diets of birds and parasitic entomophagous insects. The adults are included in food webs in a much broader range of consumers (including birds, small mammals, reptiles, etc.).[23]:567

Defense and predation

Papilio machaon caterpillar showing the osmeterium, which emits unpleasant smells to ward off predators

Lepidopteran species are soft bodied, fragile, and almost defenseless, while the immature stages move slowly or are immobile, hence all stages are exposed to predation. Adult butterflies and moths are preyed upon by birds, lizards, amphibians, dragonflies, and spiders. Caterpillars and pupae fall prey not only to birds, but also to invertebrate predators and small mammals, as well as fungi and bacteria. Parasitoid and parasitic wasps and flies may lay eggs in the caterpillar, which eventually kill it as they hatch inside its body and eat its tissues. Insect-eating birds are probably the largest predators. Lepidoptera, especially the immature stages, are an ecologically important food to many insectivorous birds, such as the great tit in Europe.

An "evolutionary arms race" can be seen between predator and prey species. The Lepidoptera have developed a number of strategies for defense and protection, including evolution of morphological characters and changes in ecological lifestyles and behaviors. These include aposematism, mimicry, camouflage, and development of threat patterns and displays.[71] Only a few birds, such as the nightjars, hunt nocturnal lepidopterans. Their main predators are bats. Again, an "evolutionary race" exists, which has led to numerous evolutionary adaptations of moths to escape from their main predators, such as the ability to hear ultrasonic sounds, or even to emit sounds in some cases. Lepidopteran eggs are also preyed upon. Some caterpillars, such as the zebra swallowtail butterfly larvae, are cannibalistic.

Some species of Lepidoptera are poisonous to predators, such as the monarch butterfly in the Americas, Atrophaneura species (roses, windmills, etc.) in Asia, as well as Papilio antimachus, and the birdwings, the largest butterflies in Africa and Asia, respectively. They obtain their toxicity by sequestering the chemicals from the plants they eat into their own tissues. Some Lepidoptera manufacture their own toxins. Predators that eat poisonous butterflies and moths may become sick and vomit violently, learning not to eat those species. A predator which has previously eaten a poisonous lepidopteran may avoid other species with similar markings in the future, thus saving many other species, as well.[71][72] Toxic butterflies and larvae tend to develop bright colors and striking patterns as an indicator to predators about their toxicity. This phenomenon is known as aposematism.[73] Some caterpillars, especially members of Papilionidae, contain an osmeterium, a Y-shaped protrusible gland found in the prothoracic segment of the larvae.[71] When threatened, the caterpillar emits unpleasant smells from the organ to ward off the predators.[74][75]

Camouflage is also an important defense strategy, which involves the use of coloration or shape to blend into the surrounding environment. Some lepidopteran species blend with their surroundings, making them difficult to spot by predators. Caterpillars can exhibit shades of green that match its host plant. Others look like inedible objects, such as twigs or leaves. For instance, the mourning cloak fades into the backdrop of trees when it folds its wings back.[76] The larvae of some species, such as the common Mormon (Papilio polytes) and the western tiger swallowtail look like bird droppings.[71][77] For example, adult Sesiidae species (also known as clearwing moths) have a general appearance sufficiently similar to a wasp or hornet to make it likely the moths gain a reduction in predation by Batesian mimicry.[78] Eyespots are a type of automimicry used by some butterflies and moths. In butterflies, the spots are composed of concentric rings of scales in different colors. The proposed role of the eyespots is to deflect attention of predators. Their resemblance to eyes provokes the predator's instinct to attack these wing patterns.[79]

Batesian and Müllerian mimicry complexes are commonly found in Lepidoptera. Genetic polymorphism and natural selection give rise to otherwise edible species (the mimic) gaining a survival advantage by resembling inedible species (the model). Such a mimicry complex is referred to as Batesian and is most commonly known in the example between the limenitidine viceroy butterfly in relation to the inedible danaine monarch. The viceroy is, in fact, more toxic than the monarch and this resemblance should be considered as a case of Müllerian mimicry.[80] In Müllerian mimicry, inedible species, usually within a taxonomic order, find it advantageous to resemble each other so as to reduce the sampling rate by predators that need to learn about the insects' inedibility. Taxa from the toxic genus Heliconius form one of the most well-known Müllerian complexes.[81] The adults of the various species now resemble each other so well, the species cannot be distinguished without close morphological observation and, in some cases, dissection or genetic analysis.

Moths evidently are able to hear the range emitted by bat]s, which in effect causes flying moths to make evasive maneuvers because bats are a main predator of moths. Ultrasonic frequencies trigger a reflex action in the noctuid moth that cause it to drop a few inches in its flight to evade attack.[82] Tiger moths in a defense emit clicks within the same range of the bats, which interfere with the bats and foil their attempts to echolocate it.[83]

Pollination

A day-flying hummingbird hawk-moth drinking nectar from a species of Dianthus

Most species of Lepidoptera engage in some form of entomophily (more specifically psychophily and phalaenophily for butterflies and moths, respectively), or the pollination of flowers.[84] Most adult butterflies and moths feed on the nectar inside flowers, using their probosces to reach the nectar hidden at the base of the petals. In the process, the adults brush against the flowers' stamens, on which the reproductive pollen is made and stored. The pollen is transferred on appendages on the adults, which fly to the next flower to feed and unwittingly deposit the pollen on the stigma of the next flower, where the pollen germinates and fertilizes the seeds.[23]:813–814

Flowers pollinated by butterflies tend to be large and flamboyant, pink or lavender in color, frequently having a landing area, and usually scented, as butterflies are typically day-flying. Since butterflies do not digest pollen (except for heliconid species,[84]) more nectar is offered than pollen. The flowers have simple nectar guides, with the nectaries usually hidden in narrow tubes or spurs, reached by the long "tongue" of the butterflies. Butterflies such as Thymelicus flavus have been observed to engage in flower constancy, which means they are more likely to transfer pollen to other conspecific plants. This can be beneficial for the plants being pollinated, as flower constancy prevents the loss of pollen during different flights and the pollinators from clogging stigmas with pollen of other flower species.[85]

Among the more important moth pollinator groups are the hawk moths of the family Sphingidae. Their behavior is similar to hummingbirds, i.e., using rapid wing beats to hover in front of flowers. Most hawk moths are nocturnal or crepuscular, so moth-pollinated flowers (e.g., Silene latifolia ) tend to be white, night-opening, large, and showy with tubular corollae and a strong, sweet scent produced in the evening, night, or early morning. A lot of nectar is produced to fuel the high metabolic rates needed to power their flight.[86] Other moths (e.g., noctuids, geometrids, pyralids) fly slowly and settle on the flower. They do not require as much nectar as the fast-flying hawk moths, and the flowers tend to be small (though they may be aggregated in heads).[87]

Mutualism


Tobacco hornworm caterpillar Manduca sexta parasitized by Braconidae wasp larvae

Mutualism is a form of biological interaction wherein each individual involved benefits in some way. An example of a mutualistic relationship would be that shared by yucca moths (Tegeculidae) and their host, yucca flowers (Liliaceae). Female yucca moths enter the host flowers, collect the pollen into a ball using specialized maxillary palps, then move to the apex of the pistil, where pollen is deposited on the stigma, and lay eggs into the base of the pistil where seeds will develop. The larvae develop in the fruit pod and feed on a portion of the seeds. Thus, both insect and plant benefit, forming a highly mutualistic relationship.[23]:814 Another form of mutualism occurs between some larvae of butterflies and certain species of ants (e. g. Lycaenidae). The larvae communicate with the ants using vibrations transmitted through a substrate, such as the wood of a tree or stems, as well as using chemical signals.[88] The ants provide some degree of protection to these larvae and they in turn gather honeydew secretions.[89]

Parasitism

Only 41 species of parasitoid lepidopterans are known (1-Pyralidae; 40-Epipyropidae).[23]:748 The larvae of the greater and lesser wax moths feed on the honeycomb inside bee nests and may become pests; they are also found in bumblebee and wasp nests, albeit to a lesser extent. In northern Europe, the wax moth is regarded as the most serious parasitoid of the bumblebee, and is found only in bumblebee nests. In some areas in southern England, as much as 80% of nests can be destroyed.[90] Other parasitic larvae are known to prey upon cicadas and leaf hoppers.[91]
Brachymeria intermedia Coccygomimus instigator Compsilura concinnata Parasetigena silvestris Blepharipa pratensis Aphantorhaphopsis samerensis Glyptapanteles liparidis Meteorus pulchricornis Cotesia melanoscelus Glyptapanteles porthetriae Hyposoter tricoloripes Phobocampe disparis Anastatus disparis
The different parasitoids affecting the gypsy moth (Lymantaria dispar): The stage they affect and eventually kill and its duration are denoted by arrows.

In reverse, moths and butterflies may be subject to parasitic wasps and flies, which may lay eggs on the caterpillars, which hatch and feed inside its body, resulting in death. Although, in a form of parasitism called idiobiont, the adult paralyzes the host, so as not to kill it but for it to live as long as possible, for the parasitic larvae to benefit the most. In another form of parasitism, koinobiont, the species live off their hosts while inside (endoparasitic). These parasites live inside the host caterpillar throughout its lifecycle, or may affect it later on as an adult. In other orders, koinobionts include flies, a majority of coleopteran, and many hymenopteran parasitoids.[23]:748–749 Some species may be subject to a variety of parasites, such as the gypsy moth (Lymantaria dispar), which is attacked by a series of 13 species, in six different taxa throughout its lifecycle.[23]:750

In response to a parsitoid egg or larva in the caterpillar's body, the plasmatocytes, or simply the host's cells can form a multilayered capsule that eventually causes the endoparasite to asphyxiate. The process, called encapsulation, is one of the caterpillar's only means of defense against parasitoids.[23]:748

Other biological interactions

A few species of Lepidoptera are secondary consumers, or predators. These species typically prey upon the eggs of other insects, aphids, scale insects, or ant larvae.[23]:567 Some caterpillars are cannibals, and others prey on caterpillars of other species (e. g. Hawaiian Eupithecia ). Those of the 15 species in Eupithecia that mirror inchworms, are the only known species of butterflies and moths that are ambush predators.[92] Four species are known to eat snails. For example, the Hawaiian caterpillar, (H. molluscivora), uses silk traps, in a manner similar to that of spiders, to capture certain species of snails (typically Tornatellides).[91]

Larvae of some species of moths in the Tineidae, Gelechioidae, and Noctuidae (family/superfamily/families, respectively), besides others, feed on detritus, or dead organic material, such as fallen leaves and fruit, fungi, and animal products, and turn it into humus.[23]:567 Well-known species include the cloth moths (Tineola bisselliella, T. pellionella, and T. tapetzella), which feed on detritus containing keratin, including hair, feathers, cobwebs, bird nests (particularly of domestic pigeons, Columba livia domestica) and fruits or vegetables. These species are important to ecosystems as they remove substances that would otherwise take a long time to decompose.[93]

Evolution and systematics

History of study

Lepidoptera collection in Cherni Osam Natural Sciences Museum, Troyan, Bulgaria

Linnaeus in Systema Naturae (1758) recognized three divisions of the Lepidoptera: Papilio, Sphinx and Phalaena, with seven subgroups in Phalaena.[94] These persist today as 9 of the superfamilies of Lepidoptera. Other works on classification followed including those by Michael Denis & Ignaz Schiffermüller (1775), Johan Christian Fabricius (1775) and Pierre André Latreille (1796). Jacob Hübner described many genera, and the Lepidopteran genera were catalogued by Ferdinand Ochsenheimer and Georg Friedrich Treitschke in a series of volumes on the Lepidopteran fauna of Europe published between 1807 and 1835.[94] Gottlieb August Wilhelm Herrich-Schäffer (several volumes, 1843–1856), and Edward Meyrick (1895) based their classifications primarily on wing venation. Sir George Francis Hampson worked on the 'Microlepidoptera' during this period and Philipp Christoph Zeller published The Natural History of the Tineinae also on Microlepidoptera (1855).

Among the first entomologists to study fossil insects and their evolution was Samuel Hubbard Scudder (1837–1911), who worked on butterflies.[95] He published a study of the Florissant deposits of Colorado, including the exceptionally preserved Prodryas persephone. Andreas V. Martynov (1879–1938) recognized the close relationship between Lepidoptera and Trichoptera in his studies on phylogeny.[95]

Major contributions in the 20th century included the creation of the monotrysia and ditrysia (based on female genital structure) by Borner in 1925 and 1939.[94] Willi Hennig (1913–1976) developed the cladistic methodology and applied it to insect phylogeny. Niels P. Kristensen, E. S. Nielsen and D. R. Davis studied the relationships among monotrysian families and Kristensen worked more generally on insect phylogeny and higher Lepidoptera too.[94][95] While it is often found that DNA-based phylogenies differ from those based on morphology, this has not been the case for the Lepidoptera; DNA phylogenies correspond to a large extent to morphology-based phylogenies.[95]

Many attempts have been made to group the superfamilies of the Lepidoptera into natural groups, most of which fail because one of the two groups is not monophyletic: Microlepidotera and Macrolepidoptera, Heterocera and Rhopalocera, Jugatae and Frenatae, Monotrysia and Ditrysia.[94]

Fossil record

1887 engraving of Prodryas persephone, a fossil Lepidopteran from the Eocene.

The fossil record for Lepidoptera is lacking in comparison to other winged species, and tending not to be as common as some other insects in the habitats that are most conducive to fossilization, such as lakes and ponds, and their juvenile stage has only the head capsule as a hard part that might be preserved. The location and abundance of the most common moth species are indicative that mass migrations of moths occurred over the Palaeogene North Sea, which is why there is a serious lack of moth fossils.[96] Yet there are fossils, some preserved in amber and some in very fine sediments. Leaf mines are also seen in fossil leaves, although the interpretation of them is tricky.[95]

Putative fossil stem group representatives of Amphiesmenoptera (the clade comprising Trichoptera and Lepidoptera) are known from the Triassic.[23]:567 The earliest known fossil lepidopteran is Archaeolepis mane from the Jurassic, about 190 million years ago in Dorset, UK.[95] The fossil belongs to a small primitive moth-like species, and its wings are showing scales with parallel grooves under a scanning electron microscope and a characteristic wing venation pattern shared with Trichoptera (Caddisflies).[95] Only two more sets of Jurassic lepidopteran fossils have been found, as well as 13 sets from the Cretaceous, which all belong to primitive moth-like families.[95] Many more fossils are found from the Tertiary, and particularly the Eocene Baltic amber. The oldest genuine butterflies of the superfamily Papilionoidea have been found in the Paleocene MoClay or Fur Formation of Denmark. The best preserved fossil lepidopteran is the Eocene Prodryas persephone from the Florissant Fossil Beds.

Phylogeny


Phylogenetic hypothesis of major lepidopteran lineages superimposed on the geologic time scale. Angiosperm radiation spans 130 to 95 million years ago from the earliest angiosperms, to angiosperm domination of vegetation.

Lepidoptera and Trichoptera (caddisflies) are more closely related to each other than to any other insect order, sharing many similarities that are lacking in others; for example the females of both orders are heterogametic, meaning they have two different sex chromosomes, whereas in most species the males are heterogametic and the females have two identical sex chromosomes. The adults in both orders display a particular wing venation pattern on their forewings. The larvae of both orders have mouth structures and gland with which they make and manipulate silk. Willi Hennig grouped the two sister orders into the Amphiesmenoptera superorder. This group probably evolved in the Jurassic, having split from the now extinct order Necrotaulidae.[95] Lepidoptera descend from a diurnal moth-like common ancestor that either fed on dead or living plants.[97]

Micropterigidae, Agathiphagidae and Heterobathmiidae are the oldest and most basal lineages of Lepidoptera. The adults of these families do not have the curled tongue or proboscis, that are found in most members order, but instead have chewing mandibles adapted for a special diet. Micropterigidae larvae feed on leaves, fungi, or liverworts (much like the Trichoptera).[94] Adult Micropterigidae chew the pollen or spores of ferns. In the Agathiphagidae, larvae live inside kauri pines and feed on seeds. In Heterobathmiidae the larvae feed on the leaves of Nothofagus, the southern beech tree. These families also have mandibles in the pupal stage, which help the pupa emerge from the seed or cocoon after metamorphosis.[94]

The Eriocraniidae have a short coiled proboscis in the adult stage, and though they retain their pupal mandibles with which they escaped the cocoon, their mandibles are non-functional thereafter.[94] Most of these non-ditrysian families, are primarily leaf miners in the larval stage. In addition to the proboscis, there is a change in the scales among these basal lineages, with later lineages showing more complex perforated scales.[95]

With the evolution of the Ditrysia in the mid-Cretaceous, there was a major reproductive change. The Ditrysia, which comprise 98% of the Lepidoptera, have two separate openings for reproduction in the females (as well as a third opening for excretion), one for mating, and one for laying eggs. The two are linked internally by a seminal duct. (In more basal lineages there is one cloaca, or later, two openings and an external sperm canal.) Of the early lineages of Ditrysia, Gracillarioidea and Gelechioidea are mostly leaf miners, but more recent lineages feed externally. In the Tineoidea, most species feed on plant and animal detritus and fungi, and build shelters in the larval stage.[95]

The Yponomeutoidea is the first group to have significant numbers of species whose larvae feed on herbaceous plants, as opposed to woody plants.[95] They evolved about the time that flowering plants underwent an expansive adaptive radiation in the mid-Cretaceous, and the Gelechioidea that evolved at this time also have great diversity. Whether the processes involved coevolution or sequential evolution, the diversity of the Lepidoptera and the angiosperms increased together.

In the so-called "Macrolepidoptera", which constitutes about 60% of lepidopteran species, there was a general increase in size, better flying ability (via changes in wing shape and linkage of the forewings and hindwings), reduction in the adult mandibles, and a change in the arrangement of the crochets (hooks) on the larval prolegs, perhaps to improve the grip on the host plant.[95] Many also have tympanal organs, that allow them to hear. These organs evolved eight times, at least, because they occur on different body parts and have structural differences.[95] The main lineages in the Macrolepidoptera are the Noctuoidea, Bombycoidea, Lasiocampidae, Mimallonoidea, Geometroidea and Rhopalocera. Bombycoidea plus Lasiocampidae plus Mimallonoidea may be a monophyletic group.[95] The Rhopalocera, comprising the Papilionoidea (butterflies), Hesperioidea (skippers), and the Hedyloidea (moth-butterflies), are the most recently evolved.[94] There is quite a good fossil record for this group, with the oldest skipper dating from 56 million years ago.[95]

Taxonomy

Taxonomy is the classification of species in selected taxa, the process of naming being called nomenclature. There are over 120 families in lepidoptera, in 45 to 48 superfamilies. Lepidoptera have always been, historically, classified in five suborders, one of which is of primitive moths that never lost the morphological features of its ancestors. The rest of the moths and butterflies make up ninety-eight percent of the other taxa, making Ditrysia. More recently, findings of new taxa, larvae and pupa have aided in detailing the relationships of primitive taxa, phylogenetic analysis showing the primitive lineages to be paraphyletic compared to the rest of Lepidoptera lineages. Recently lepidopterists have abandoned clades like suborders, and those between orders and superfamilies.[23]:569
  • Zeugloptera is a clade with Micropterigoidea being its only superfamily, containing the single family Micropterigidae. Species of Micropterigoidea are practically living fossils, being one of the most primitive lepidopteran groups, still retaining chewing mouthparts (mandibles) in adults, unlike other clades of butterflies and moths. About 120 species are known worldwide, with more than half the species in the genus Micropteryx in the Paleartic region. There are only 2 known in North America (Epimartyria), with many more being found Asia and the southwest Pacific, particularly New Zealand with about 50 species.[23]:569
  • Glossata contains a majority of the species, with the most obvious difference is non-functioning mandibles, and elongated maxillary galeae or the proboscis. The basal clades still retaining some of the ancestral features of the wings such as similarly shaped fore- and hindwings with relatively complete venation. Glossata also contains the division Ditrysia, which contains 98% of all described species in Lepidoptera.[23]:569
  • Heterobathmiina was first described by Kristensen and Nielsen in 1979. There are about 10 species, which are day-flying, metallic moths, confined to southern South America, the adults eat the pollen of Nothofagus or Southern Beech and the larvae mine the leaves.[23]:569[101]

Relationship to people

Culture


Death's-head Hawkmoth (Acherontia lachesis), an old bleached specimen still showing the classical skull-shaped head

Artistic depictions of butterflies have been used in many cultures including as early as 3500 years ago, in Egyptian hieroglyphs.[102] Today, butterflies are widely used in various objects of art and jewelry: mounted in frames, embedded in resin, displayed in bottles, laminated in paper, and in some mixed media artworks and furnishings.[103] Butterflies have also inspired the "butterfly fairy" as an art and fictional character.

In many cultures the soul of a dead person is associated with the butterfly. As in Ancient Greece, where the word for butterfly ψυχή (psyche) also means soul and breath. In Latin, as in Ancient Greece, the word for "butterfly" papilio was associated with the soul of the dead.[104] The skull-like marking on the thorax of the Death's-head Hawkmoth has helped these moths, particularly A. atropos, earn a negative reputation, such as associations with the supernatural and evil. The moth has been prominently featured in art and movies such as Un Chien Andalou (by Buñuel and Dalí) and The Silence of the Lambs, and in the artwork of the Japanese metal band Sigh's album Hail Horror Hail. According to Kwaidan: Stories and Studies of Strange Things, by Lafcadio Hearn, a butterfly was seen in Japan 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.[105]

In the ancient Mesoamerican city of Teotihuacan, the brilliantly colored image of the butterfly was carved into many temples, buildings, jewelry, and emblazoned on incense burners in particular. The butterfly was sometimes depicted with the maw of a jaguar and some species were considered to be the reincarnations of the souls of dead warriors. The close association of butterflies to fire and warfare persisted through to the Aztec civilization and evidence of similar jaguar-butterfly images has been found among the Zapotec, and Maya civilizations.[106]
Caterpillar hatchling of the Grey Dagger (Acronicta psi) eating leaves from a tree

Pests

The larvae of many Lepidopteran species are major pests in agriculture. Some of the major pests include Tortricidae, Noctuidae, and Pyralidae. The larvae of the Noctuidae genus Spodoptera (armyworms), Helicoverpa (corn earworm), or Pieris brassicae can cause extensive damage to certain crops.[94] Helicoverpa zea larvae (cotton bollworms or tomato fruitworms) are polyphagous, meaning they eat a variety of crops, including tomatoes and cotton.[107]

Butterflies and moths are one of the largest taxa to solely feed and be dependent on living plants, in terms of the number of species, and they are in many ecosystems, making up the largest biomass to do so. In many species, the female may produce anywhere from 200 to 600 eggs, while in some others it may go as high as 30,000 eggs in one day. This can create many problems for agriculture, where many caterpillars can affect acres of vegetation. Some reports estimate that there have been over 80,000 caterpillars of several different taxa feeding on a single oak tree. In some cases, phytophagous larvae can lead to the destruction of entire trees in relatively short periods of time.[23]:567

Ecological ways of removing pest lepidoptera species are becoming more economically viable, as research has shown ways like introducing parasitic wasp and flies. For example Sarcophaga aldrichi, a fly which deposited larvae feed upon the pupae of the Forest Tent Caterpillar Moth. Pesticides can affect other species other than the species they are targeted to eliminate, damaging the natural ecosystem.[108] Another good biological pest control method is the use of pheromone traps. A pheromone trap is a type of insect trap that uses pheromones to lure insects. Sex pheromones and aggregating pheromones are the most common types used. A pheromone-impregnated lure is encased in a conventional trap such as a Delta trap, water-pan trap, or funnel trap.[109]

Species of moths that are detritivores would naturally eat detritus containing keratin, such as hairs or feathers. Well known species are cloth moths (T. bisselliella, T. pellionella, and T. tapetzella), feeding on foodstuffs that people find economically important, such as cotton, linen, silk and wool fabrics as well as furs; furthermore they have been found on shed feathers and hair, bran, semolina and flour (possibly preferring wheat flour), biscuits, casein, and insect specimens in museums.[93]

Beneficial insects

Even though most butterflies and moths affect the economy negatively, some species are a valuable economic resource. The most prominent example is that of the Domesticated silkworm moth (Bombyx mori), the larvae of which make their cocoons out of silk, which can be spun into cloth. Silk is and has been an important economic resource throughout history. The species Bombyx mori has been domesticated to the point where it is completely dependent on mankind for survival.[110] A number of wild moths such as Bombyx mandarina, and Antheraea species, besides others, provide commercially important silks.[111]

The preference of the larvae of most Lepidopteran species to feed on a single species or limited range of plants is used as a mechanism for biological control of weeds in place of herbicides. The pyralid cactus moth was introduced from Argentina to Australia, where it successfully suppressed millions of acres of Prickly pear cactus.[23]:567 Another species of the Pyralidae, called the alligator weed stem borer (Arcola malloi), was used to control the aquatic plant known as alligator weed (Alternanthera philoxeroides) in conjunction with the alligator weed flea beetle; in this case, the two insects work in synergy and the weed rarely recovers.[112]

Breeding butterflies and moths, or butterfly gardening/rearing, has become an ecologically viable process of introducing species into the ecosystem to benefit it. Butterfly ranching in Papua New Guinea permits nationals of that country to 'farm' economically valuable insect species for the collectors market in an ecologically sustainable manner.[113]

Food


Beondegi, silkworm pupae steamed or boiled and seasoned for taste, for sale by a street vendor in South Korea

Lepidoptera feature prominently in entomophagy as food items on almost every continent. While in most cases, adults, larvae or pupae are eaten as staples by indigenous people, beondegi or silkworm pupae are eaten as a snack in Korean cuisine[114] while Maguey worm is considered a delicacy in Mexico.[115] In the Carnia region of Italy, children catch and eat ingluvies of the toxic Zygaena moths in early summer. The ingluvies, despite having a very low cyanogenic content, serve as a convenient, supplementary source of sugar to the children who can include this resource as a seasonal delicacy at minimum risk.[116]

Health

Some larvae of both moths and butterflies have a form of hair that has been known to be a cause of human health problems. Caterpillar hairs sometimes have toxins in them and species from approximately 12 families of moths or butterflies worldwide can inflict serious human injuries (Urticarial dermatitis and atopic asthma to osteochondritis, consumption coagulopathy, renal failure, and intracerebral hemorrhage).[117] Skin rashes are the most common, but there have been fatalities.[118] Lonomia is a frequent cause of economization in humans in Brazil, with 354 cases reported between 1989 and 2005. Lethality ranging up to 20% with death caused most often by intracranial hemorrhage.[119]

These hairs have also been known to cause kerato-conjunctivitis. The sharp barbs on the end of caterpillar hairs can get lodged in soft tissues and mucous membranes such as the eyes. Once they enter such tissues, they can be difficult to extract, often exacerbating the problem as they migrate across the membrane.[120] This becomes a particular problem in an indoor setting. The hairs easily enter buildings through ventilation systems and accumulate in indoor environments because of their small size, which makes it difficult for them to be vented out. This accumulation increases the risk of human contact in indoor environments.[121]

Bee


From Wikipedia, the free encyclopedia

Bee
Temporal range: Early Cretaceous – Recent, 100–0Ma
Honeybee landing on milkthistle02.jpg
Apis mellifera (Honeybee).
Scientific classification e
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Suborder: Apocrita
Superfamily: Apoidea
Clade: Anthophila
Families
Andrenidae
Apidae
Colletidae
Dasypodaidae
Halictidae
Megachilidae
Meganomiidae
Melittidae
Stenotritidae
Synonyms
Apiformes

Bees are flying insects closely related to wasps and ants, and are known for their role in pollination and for producing honey and beeswax. Bees are a monophyletic lineage within the superfamily Apoidea, presently considered as a clade Anthophila. There are nearly 20,000 known species of bees in seven to nine recognized families,[1] though many are undescribed and the actual number is probably higher. They are found on every continent except Antarctica, in every habitat on the planet that contains insect-pollinated flowering plants.

Bees are adapted for feeding on nectar and pollen, the former primarily as an energy source and the latter primarily for protein and other nutrients. Most pollen is used as food for larvae.

Bees have a long proboscis (a complex "tongue") that enables them to obtain the nectar from flowers. They have antennae almost universally made up of 13 segments in males and 12 in females, as is typical for the superfamily. Bees all have two pairs of wings, the hind pair being the smaller of the two; in a very few species, one sex or caste has relatively short wings that make flight difficult or impossible, but none are wingless.

Tiny stingless bee species exist whose workers are less than 2 mm (0.079 in) long.[2] The largest bee in the world is Megachile pluto, a leafcutter bee whose females can attain a length of 39 mm (1.5"). Members of the family Halictidae, or sweat bees, are the most common type of bee in the Northern Hemisphere, though they are small and often mistaken for wasps or flies.

The best-known bee species is the European honey bee, which, as its name suggests, produces honey, as do a few other types of bee. Human management of this species is known as beekeeping or apiculture.

Bees are the favorite meal of Merops apiaster, the bee-eater (a bird). Other common predators are kingbirds, mockingbirds, beewolves, and dragonflies.

Evolution

The ancestors of bees were wasps in the family Crabronidae, and therefore predators of other insects. The switch from insect prey to pollen may have resulted from the consumption of prey insects which were flower visitors and were partially covered with pollen when they were fed to the wasp larvae. This same evolutionary scenario may also have occurred within the vespoid wasps, where the group known as "pollen wasps" also evolved from predatory ancestors. Up until recently, the oldest non-compression bee fossil had been Cretotrigona prisca in New Jersey amber and of Cretaceous age, a meliponine. A recently reported bee fossil, of the genus Melittosphex, is considered "an extinct lineage of pollen-collecting Apoidea sister to the modern bees", and dates from the early Cretaceous (~100 mya).[3] Derived features of its morphology ("apomorphies") place it clearly within the bees, but it retains two unmodified ancestral traits ("plesiomorphies") of the legs (two mid-tibial spurs, and a slender hind basitarsus), indicative of its transitional status.

The earliest animal-pollinated flowers were pollinated by insects such as beetles, so the syndrome of insect pollination was well established before bees first appeared. The novelty is that bees are specialized as pollination agents, with behavioral and physical modifications that specifically enhance pollination, and are generally more efficient at the task than any other pollinating insect such as beetles, flies, butterflies and pollen wasps. The appearance of such floral specialists is believed to have driven the adaptive radiation of the angiosperms, and, in turn, the bees themselves.

Among living bee groups, the "short-tongued" bee family Colletidae has traditionally been considered the most "primitive", and sister taxon to the remainder of the bees. In the 21st century, however, some researchers have claimed that the Dasypodaidae is the basal group, the short, wasp-like mouthparts of colletids being the result of convergent evolution, rather than indicative of a plesiomorphic condition.[1] This subject is still under debate, and the phylogenetic relationships among bee families are poorly understood.

Eusocial and semisocial bees


A honey bee swarm

Honey bees defend against wasp attacks

Bees may be solitary or may live in various types of communities. The most advanced of these are eusocial colonies[4] found among the honey bees, bumblebees, and stingless bees. Sociality, of several different types, is believed to have evolved separately many times within the bees.

In some species, groups of cohabiting females may be sisters, and if there is a division of labor within the group, then they are considered semisocial.

If, in addition to a division of labor, the group consists of a mother and her daughters, then the group is called eusocial. The mother is considered the queen and the daughters are workers. These castes may be purely behavioral alternatives, in which case the system is considered "primitively eusocial" (similar to many paper wasps), and if the castes are morphologically discrete, then the system is "highly eusocial".

There are many more species of primitively eusocial bees than highly eusocial bees, but they have rarely been studied. The biology of most such species is almost completely unknown. The vast majority are in the family Halictidae, or "sweat bees". Colonies are typically small, with a dozen or fewer workers, on average. The only physical difference between queens and workers is average size, if they differ at all. Most species have a single season colony cycle, even in the tropics, and only mated females (future queens, or "gynes") hibernate (called diapause). A few species have long active seasons and attain colony sizes in the hundreds. The orchid bees include a number of primitively eusocial species with similar biology. Certain species of allodapine bees (relatives of carpenter bees) also have primitively eusocial colonies, with unusual levels of interaction between the adult bees and the developing brood. This is "progressive provisioning"; a larva's food is supplied gradually as it develops. This system is also seen in honey bees and some bumblebees.

Thanks to new molecular phylogeny data, a timeline of the evolution of eusocial bee species is available. The complexity of social behaviors seems positively correlated with age of evolutionary origin. This ranges from around 21 Mya in Halictidae, 53 Mya in alodapines, with the corbiculate Apidae being the oldest at roughly 87 Mya.[5]

Highly eusocial bees live in colonies. Each colony has a single queen, many workers and, at certain stages in the colony cycle, drones. When humans provide the nest, it is called a hive. Honey bee hives can contain up to 40,000 bees at their annual peak, which occurs in the spring, but usually have fewer.

Bumblebees

Bumblebees (Bombus terrestris, Bombus pratorum, et al.) are eusocial in a manner quite similar to the eusocial Vespidae such as hornets. The queen initiates a nest on her own (unlike queens of honey bees and stingless bees which start nests via swarms in the company of a large worker force). 
Bumblebee colonies typically have from 50 to 200 bees at peak population, which occurs in mid to late summer. Nest architecture is simple, limited by the size of the nest cavity (pre-existing), and colonies are rarely perennial. Bumblebee queens sometimes seek winter safety in honey bee hives, where they are sometimes found dead in the spring by beekeepers, presumably stung to death by the honey bees. It is unknown whether any survive winter in such an environment.
Bumblebees are one of the more important wild pollinators, but have declined significantly in recent decades. In the UK, two species have become nationally extinct during the last 75 years while others have been placed on the UK Biodiversity Action Plan as priority species in recognition of the need for conservation action. In 2006 a new charity, the Bumblebee Conservation Trust, was established to coordinate efforts to conserve remaining populations through conservation and education. In 2011, the International Union for the Conservation of Nature set up the Bumblebee Specialist Group to review the threat status of all bumblebee species world-wide using the IUCN Red List criteria.[6]

Stingless bees

Stingless bees are very diverse in behavior, but all are highly eusocial. They practise mass provisioning, complex nest architecture, and perennial colonies.

Honey bees


An African bee Apis mellifera subspecies scutellata, extracts nectar from a flower as pollen grains stick to its body in Tanzania

The true honey bees (genus Apis) have arguably the most complex social behavior among the bees, is the best known bee species, and one of the best known of all insects. There are 29 subspecies of Apis mellifera, native to Europe, the Middle East, and Africa.

Africanized honey bee

Africanized bees, also called killer bees, are a hybrid strain of Apis mellifera derived from experiments by Warwick Estevam Kerr to cross European and African honey bee subspecies. Several queen bees escaped from his laboratory in South America and have spread throughout the Americas. Africanized honey bees are more defensive than European honey bees.

Solitary and communal bees

Most other bees, including familiar species of bee such as the Eastern carpenter bee (Xylocopa virginica), alfalfa leafcutter bee (Megachile rotundata), orchard mason bee (Osmia lignaria) and the hornfaced bee (Osmia cornifrons) are solitary in the sense that every female is fertile, and typically inhabits a nest she constructs herself. There are no worker bees for these species. Solitary bees typically produce neither honey nor beeswax. They are immune from acarine and Varroa mites, but have their own unique parasites, pests and diseases (see also diseases of the honey bee).

Solitary bees are important pollinators, and pollen is gathered for provisioning the nest with food for their brood. Often it is mixed with nectar to form a paste-like consistency. Some solitary bees have very advanced types of pollen-carrying structures on their bodies. A very few species of solitary bees are being increasingly cultured for commercial pollination. Most of these species belong to a distinct set of genera, namely: carpenter bees, sweat bees, mason bees, polyester bees, squash bees, dwarf carpenter bees, leafcutter bees, alkali bees, digger bees.[7][8]

A solitary bee, Anthidium florentinum (family Megachilidae), visiting Lantana

Solitary bees are often oligoleges, in that they only gather pollen from one or a few species/genera of plants (unlike honey bees and bumblebees which are generalists). No known bees are nectar specialists; many oligolectic bees will visit multiple plants for nectar, but there are no bees which visit only one plant for nectar while also gathering pollen from many different sources. Specialist pollinators also include bee species which gather floral oils instead of pollen, and male orchid bees, which gather aromatic compounds from orchids (one of the only cases where male bees are effective pollinators). In a very few cases only one species of bee can effectively pollinate a plant species, and some plants are endangered at least in part because their pollinator is dying off. There is, however, a pronounced tendency for oligolectic bees to be associated with common, widespread plants which are visited by multiple pollinators (e.g., there are some 40 oligoleges associated with creosote bush in the US desert southwest,[9] and a similar pattern is seen in sunflowers, asters, mesquite, etc.)

Solitary bees create nests in hollow reeds or twigs, holes in wood, or, most commonly, in tunnels in the ground. The female typically creates a compartment (a "cell") with an egg and some provisions for the resulting larva, then seals it off. A nest may consist of numerous cells. When the nest is in wood, usually the last (those closer to the entrance) contain eggs that will become males. The adult does not provide care for the brood once the egg is laid, and usually dies after making one or more nests. The males typically emerge first and are ready for mating when the females emerge. Providing nest boxes for solitary bees is increasingly popular among gardeners. Solitary bees are either stingless or very unlikely to sting (only in self-defense, if ever).

While solitary females each make individual nests, some species are gregarious, preferring to make nests near others of the same species, giving the appearance to the casual observer that they are social. Large groups of solitary bee nests are called aggregations, to distinguish them from colonies.

In some species, multiple females share a common nest, but each makes and provisions her own cells independently. This type of group is called "communal" and is not uncommon. The primary advantage appears to be that a nest entrance is easier to defend from predators and parasites when there are multiple females using that same entrance on a regular basis.

Brood parasites


Bombus vestalis, a cuckoo bee parasite of the bumblebee Bombus terrestris

Brood parasites occur in several bee families including the apid subfamily Nomadinae. Females of these bees lack pollen collecting structures (the scopa) and do not construct their own nests. They typically enter the nests of pollen collecting species, and lay their eggs in cells provisioned by the host bee. When the cuckoo bee larva hatches it consumes the host larva's pollen ball, and kills and eats the host larva.[citation needed]

The cuckoo bees in the Bombus subgenus Psithyrus are closely related to, and resemble, their hosts in looks and size. This common pattern gave rise to the ecological principle "Emery's Rule". Others parasitize bees in different families, like Townsendiella, a nomadine apid, one species of which is a cleptoparasite of the dasypodaid genus Hesperapis, while the other species in the same genus attack halictid bees.[citation needed]

Nocturnal bees

Four bee families (Andrenidae, Colletidae, Halictidae, and Apidae) contain some species that are crepuscular (these may be either the vespertine or matinal type). These bees have greatly enlarged ocelli, which are extremely sensitive to light and dark, though incapable of forming images. Many are pollinators of flowers that themselves are crepuscular, such as evening primroses, and some live in desert habitats where daytime temperatures are extremely high.

Flight


Honeybee in mid air flight carrying pollen in pollen basket

In Antoine Magnan's 1934 book Le vol des insectes, he wrote that he and André Sainte-Laguë had applied the equations of air resistance to insects and found that their flight could not be explained by fixed-wing calculations, but that "One shouldn't be surprised that the results of the calculations don't square with reality".[10] This has led to a common misconception that bees "violate aerodynamic theory", but in fact it merely confirms that bees do not engage in fixed-wing flight, and that their flight is explained by other mechanics, such as those used by helicopters.[11]

In 1996, Charlie Ellington at Cambridge University showed that vortices created by many insects’ wings and non-linear effects were a vital source of lift;[12] vortices and non-linear phenomena are notoriously difficult areas of hydrodynamics, which has made for slow progress in theoretical understanding of insect flight.

In 2005, Michael Dickinson and his Caltech colleagues studied honey bee flight with the assistance of high-speed cinematography[13] and a giant robotic mock-up of a bee wing.[14] Their analysis revealed that sufficient lift was generated by "the unconventional combination of short, choppy wing strokes, a rapid rotation of the wing as it flops over and reverses direction, and a very fast wing-beat frequency". Wing-beat frequency normally increases as size decreases, but as the bee's wing beat covers such a small arc, it flaps approximately 230 times per second, faster than a fruitfly (200 times per second) which is 80 times smaller.[15]

Pollination

Squash bees are important pollinators of the plant genus Cucurbita and closely related plants, such as cucumbers

Bees play an important role in pollinating flowering plants, and are the major type of pollinator in ecosystems that contain flowering plants. Bees either focus on gathering nectar or on gathering pollen depending on demand, especially in social species. Bees gathering nectar may accomplish pollination, but bees that are deliberately gathering pollen are more efficient pollinators. It is estimated that one third of the human food supply depends on insect pollination, most of which is accomplished by bees, especially the domesticated European honey bee.[citation needed] Contract pollination has overtaken the role of honey production for beekeepers in many countries. Monoculture and the massive decline of many bee species (both wild and domesticated) have increasingly caused honey bee keepers to become migratory so that bees can be concentrated in seasonally varying high-demand areas of pollination.

Most bees are fuzzy and carry an electrostatic charge, which aids in the adherence of pollen. Female bees periodically stop foraging and groom themselves to pack the pollen into the scopa, which is on the legs in most bees, and on the ventral abdomen on others, and modified into specialized pollen baskets on the legs of honey bees and their relatives. Many bees are opportunistic foragers, and will gather pollen from a variety of plants, while others are oligolectic, gathering pollen from only one or a few types of plant. A small number of plants produce nutritious floral oils rather than pollen, which are gathered and used by oligolectic bees. One small subgroup of stingless bees, called "vulture bees," is specialized to feed on carrion, and these are the only bees that do not use plant products as food. Pollen and nectar are usually combined to form a "provision mass", which is often soupy, but can be firm. It is formed into various shapes (typically spheroid), and stored in a small chamber (a "cell"), with the egg deposited on the mass. The cell is typically sealed after the egg is laid, and the adult and larva never interact directly (a system called "mass provisioning").

In New Zealand scientists discovered that three genera of native bees have evolved to open flower buds of the native mistletoe Peraxilla tetrapetala. The buds cannot open themselves but are visited by birds such as the tui and bellbird which twist the top of the ripe bud. That action releases a mechanism which causes the petals to suddenly spring open, giving access to the nectar and pollen. However, when observing the native bees in the Canterbury province in the South Island, the scientists were astonished to see the bees biting the top off the buds, then pushing with their legs, occasionally popping open the buds to allow the bees to harvest the nectar and pollen, and therefore aid in the pollination of the mistletoe which is in decline in New Zealand. Nowhere else in the world have bees demonstrated ability to open explosive bird-adapted flowers.[16]

Visiting flowers can be a dangerous occupation. Many assassin bugs and crab spiders hide in flowers to capture unwary bees. Other bees are lost to birds in flight. Insecticides used on blooming plants kill many bees, both by direct poisoning and by contamination of their food supply. A honey bee queen may lay 2000 eggs per day during spring buildup, but she also must lay 1000 to 1500 eggs per day during the foraging season, mostly to replace daily casualties, most of which are workers dying of old age. Among solitary and primitively social bees, however, lifetime reproduction is among the lowest of all insects, as it is common for females of such species to produce fewer than 25 offspring.

The population value of bees depends partly on the individual efficiency of the bees, but also on the population itself. Thus while bumblebees have been found to be about ten times more efficient pollinators on cucurbits, the total efficiency of a colony of honey bees is much greater due to greater numbers. Likewise during early spring orchard blossoms, bumblebee populations are limited to only a few queens, and thus are not significant pollinators of early fruit.

Bees and humans


Bee larvae as food in Java

Former coat of arms of Abella de la Conca, Lleida, Spain

Bees figure prominently in mythology and folklore and have been used by political theorists as a model for human society. Journalist Bee Wilson states that the image of a community of honey bees "occurs from ancient to modern times, in Aristotle and Plato; in Virgil and Seneca; in Erasmus and Shakespeare; Tolstoy, as well as by social theorists Bernard Mandeville and Karl Marx."[17] They are found in heraldry where they can signify industriousness as in the Manchester bee in the crest of Manchester City Council.

In English folklore, bees would be told of important events in the household, in a custom known as "Telling the bees".[18]

Despite the honey bee's painful sting and the stereotype of insects as pests, bees are generally held in high regard. This is most likely due to their usefulness as pollinators and as producers of honey, their social nature, and their reputation for diligence. Bees are one of the few insects frequently used in advertisements in a positive manner, typically for products containing honey (such as Honey Nut Cheerios).

In ancient Egypt, the bee was seen to symbolize the lands of Lower Egypt, with the Pharaoh being referred to as "He of Sedge and Bee" (the sedge representing Upper Egypt).

In North America, yellowjackets and hornets, especially when encountered as flying pests, are often misidentified as bees, despite numerous differences between them.

Although a bee sting can be deadly to those with allergies, virtually all bee species are non-aggressive if undisturbed and many cannot sting at all. Humans are often a greater danger to bees, as bees can be affected or even harmed by encounters with toxic chemicals in the environment (see also bees and toxic chemicals).

In Indonesia bee larvae are eaten as a companion to rice, after being mixed with shredded coconut "meat", wrapped in banana leaves, and steamed.

Pollinator decline


Morphology of a female honey bee

From 1972 to 2006, there was a dramatic reduction in the number of feral honey bees in the US, which are now almost absent.[19] At the same time there was a significant though somewhat gradual decline in the number of colonies maintained by beekeepers. This decline includes the cumulative losses from all factors, such as urbanization, systematic pesticide use, tracheal and Varroa mites, and commercial beekeepers' retiring and going out of business. However, in late 2006 and early 2007 the rate of attrition reached new proportions, and the term colony collapse disorder was coined to describe the sudden disappearances.[20]

After several years of research and concern, a team of scientists headed by Jerry Bromenshenk published a paper in October 2010 saying that a new DNA-based virus, invertebrate iridescent virus or IIV6, and the fungus Nosema ceranae were found in every killed colony the group studied. In their study they found that neither agent alone seemed deadly, but a combination of the virus and Nosema ceraneae was always 100% fatal. Bromenshenk said it is not yet clear whether one condition weakens the bees enough to be finished off by the second, or whether they somehow compound the other’s destructive power. "They're co-factors, that's all we can say at the moment. They're both present in all these collapsed colonies."[21][22][23] Investigations into the phenomenon had occurred amidst great concern over the nature and extent of the losses.[24] In 2009 some reports from the US suggested that 1/3 of the honey bee colonies did not survive the winter,[25] though normal winter losses are known to be around 25%.[26] At the end of May 2012, the Swiss government reported that about half of the bee population had not survived the winter. The main cause of the decline was thought to be the parasite varroa.[27]

Apart from colony collapse disorder, many of the losses outside the US have also been attributed to other causes. Pesticides used to treat seeds, such as Clothianidin, Imidacloprid and Thiamethoxam, have been considered prime suspects.[28][29][30] Other species of bees such as mason bees are increasingly cultured and used to meet the agricultural pollination need.[31]

Native pollinators include bumblebees and solitary bees, which often survive in refuges in wild areas away from agricultural spraying, but may still be poisoned in massive spray programs for mosquitoes, gypsy moths, or other insect pests. Although pesticide use remains a concern, the major problem for wild pollinator populations is the loss of the flower-rich habitat on which they depend for food.[citation needed] Throughout the northern hemisphere, the last 70 or so years have seen an intensification of agricultural systems, which has decreased the abundance and diversity of wild flowers.[32]

Legislation such as the UK's Bees Act 1980 is designed to stop the decline of bees.[33] In April 2013 the European Union announced plans to restrict the use of certain pesticides to stop bee populations from declining further.[34]

In 2014 the Intergovernmental Panel on Climate Change report warned that bees and other pollinators faced increased risk of extinction because of global warming. This was due to their natural habitats moving and the alteration in the seasonal behaviour of species.[35] Climate change was causing the natural foraging areas for bees to change location but the bees were not always be able to move to these new areas. Bees were also emerging at different times in the year due to global warming when flowering plants were not available.

Streaming algorithm

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Streaming_algorithm ...