Peppered moth

The wingspan ranges from with a median of . It is relatively stout-bodied, with forewings relatively narrow-elongate. The wings are white, "peppered" with black, and with more-or-less distinct cross lines, also black. These transverse wing lines and "peppered" maculation (spotting) can also, in rare instances, be gray or brown; the spotting pattern, in particularly very rare cases, is sometimes a combination of brown and black/gray. The black speckling varies in amount, in some examples it is almost absent, whilst in others it is so dense that the wings appear to be black sprinkled with white. The antennae of males are strongly bipectinate. Prout (1912–16) gives an account of the forms and congeners. (MHNT) Biston betularia - Lustenice Czech Republic - Male dorsal.jpg|Biston betularia ♂ (MHNT) Biston betularia - Lustenice Czech Republic - Male ventral.jpg|Biston betularia ♂ △ == Distribution ==

Biston betularia is found in China (Heilongjiang, Jilin, Inner Mongolia, Beijing, Hebei, Shanxi, Shandong, Henan, Shaanxi, Ningxia, Gansu, Qinghai, Xinjiang, Fujian, Sichuan, Yunnan, Tibet), Russia, Mongolia, Japan, North Korea, South Korea, Nepal, Kazakhstan, Kyrgyzstan, Turkmenistan, Georgia, Azerbaijan, Armenia, Europe and North America. == Ecology and life cycle ==

. In Great Britain and Ireland, the peppered moth is univoltine (i.e., it has one generation per year), whilst in south-eastern North America it is bivoltine (two generations per year). The lepidopteran life cycle consists of four stages: ova (eggs), several larval instars (caterpillars), pupae, which overwinter in the soil, and imagines (adults). During the day, the moths typically rest on trees, where they are preyed on by birds. The caterpillar is a twig mimic, varying in colour between green and brown. On a historical note, it was one of the first animals to be identified as being camouflaged with countershading to make it appear flat (shading being the main visual cue that makes things appear solid), in a paper by Edward Bagnall Poulton in 1887. Research indicates that the caterpillars can sense the twig's colour with their skin and match their body colour to the background to protect themselves from predators, an ability to camouflage themselves also found in cephalopods, chameleons and some fish, although this colour change is rather slower in the caterpillars. == Polymorphism ==

Introduction on forms There are several melanic and non-melanic morphs of the peppered moth. These are controlled genetically. A particular colour morph can be indicated in a standard way by following the species name in the form "morpha morph name". The use of "form" in the method of Biston betularia f. formname in detailing these variations is also a widespread practice. These forms are often accidentally elevated to subspecies status when they appear in literature. Not adding the "f." (forma) or morpha implies that the taxon is a subspecies instead of a form, as in Biston betularia carbonaria instead of Biston betularia f. carbonaria. Rarely, forms have been elevated to species status, as in Biston carbonaria. Either of these two circumstances might lead to the erroneous belief that speciation was involved in the observed evolution of the peppered moth. This is not the case; individuals of each morph interbreed and produce fertile offspring with individuals of all other morphs; hence there is only one peppered moth species. By contrast, different subspecies of the same species can theoretically interbreed with one another and will produce fully fertile and healthy offspring, but in practice do not, as they live in different regions or reproduce in different seasons. Full-fledged species are either unable to produce fertile and healthy offspring, or do not recognize each other's courtship signals, or both. European breeding experiments have shown that in Biston betularia betularia, the allele for melanism producing morpha carbonaria is controlled by a single locus. The melanic allele is dominant to the non-melanic allele. This situation is, however, somewhat complicated by the presence of three other alleles that produce indistinguishable morphs of morpha medionigra. These are of intermediate dominance, but this is not complete (Majerus, 1998). Form names In continental Europe, there are three morphs: the white morph typica (syn. morpha/f. betularia), the dark melanistic morph carbonaria (syn. doubledayaria), and an intermediate form medionigra. In Britain, the typical white morph is known as typica, the melanic morph is carbonaria, and the intermediate phenotype is named insularia. In North America, the melanic black morph is morpha swettaria. In Biston betularia cognataria, the melanic allele (producing morpha swettaria) is similarly dominant to the non-melanic allele. There are also some intermediate morphs. In Japan, no melanic morphs have been recorded; they are all morpha typica. == Evolution ==

The evolution of the peppered moth over the last two hundred years has been studied in detail. At the start of this period, the vast majority of peppered moths had light coloured wing patterns which effectively camouflaged them against the light-coloured trees and lichens upon which they rested. However, due to widespread pollution during the Industrial Revolution in England, many of the lichens died out, and the trees which peppered moths rested on became blackened by soot, causing most of the light-coloured moths, or typica, to die off due to predation. At the same time, the dark-coloured, or melanic, moths, carbonaria, flourished because they could hide on the darkened trees. Since then, with improved environmental standards, light-coloured peppered moths have again become common, and the dramatic change in the peppered moth's population has remained a subject of much interest and study. This has led to the coining of the term "industrial melanism" to refer to the genetic darkening of species in response to pollutants. As a result of the relatively simple and easy-to-understand circumstances of the adaptation, the peppered moth has become a common example used in explaining or demonstrating natural selection to laypeople and classroom students through simulations. The first carbonaria morph was recorded by Edleston in Manchester in 1848, and over the subsequent years it increased in frequency. Predation experiments, particularly by Bernard Kettlewell, established that the agent of selection was birds who preyed on the carbonaria morph. Subsequent experiments and observations have supported the initial evolutionary explanation of the phenomenon. Genetic basis of melanism The evolution of the industrial melanism mutation has been shown to be due to the insertion of a transposable element into the first intron of the cortex gene, resulting in an increase in the abundance of the cortex transcript, which is expressed in developing wings. == Gallery ==

File:Biston betularia parva male.JPG|Subspecies parva (male) File:Biston betularia parva female.JPG|Subspecies parva (female) File:Biston betularia nepalensis male.jpg|Subspecies Biston betularia nepalensis (male) File:Biston betularia nepalensis female.jpg|Subspecies nepalensis (female) ==References== == External links ==