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Papilio dardanus, the Saharan swallowtail, African swallowtail, mocker swallowtail or flying handkerchief, is a species of in the family (the swallowtails). The species is broadly distributed throughout Sub-Saharan Africa. The British E. B. Poulton described it as "the most interesting butterfly in the world".


Classification
Molecular studies have provided evidence that this species' is , with Papilio constantinus being the next closest (see images below). It is a member of the of which Papilio appalachiensis and are also members.

Papilio dardanus is the nominal member of the dardanus . The members of the are:

  • Papilio dardanus Brown, 1776
  • Papilio constantinus Ward, 1871
  • Papilio delalandei Godart, 1824
  • Cramer, 1775
  • Oberthür, 1886


Subspecies
Listed alphabetically: Papilio dardanus, funet.fi
  • P. d. antinorii Oberthür, 1883 Oberthür, C., 1883 Spedezione Italiana nell Africa Equatoriale risulati zoologicae Lepidotteri:Rhopalocera Parte Seconda Ann. Mus. Stor. nat. Genova 18: 711 Full text (highlands of Ethiopia)
  • P. d. byatti Poulton, 1926 Poulton, E.B. 1926 Proceedings of the Royal Entomological Society of London. 1: xlv (northern highlands of Somalia)
  • P. d. cenea Stoll, 1790 Stoll, C 1790 Die Uitlandsche Kapellen voorkomende in de drie waerrelddeelen Asia, Africa en America Amsterdam (2-5): 134 Full text (southern Mozambique, eastern Zimbabwe, Botswana, South Africa, Eswatini)
  • P. d. dardanus Brown, 1776 (Senegal, Guinea Bissau, Guinea, Sierra Leone, Liberia, Ivory Coast, Ghana, Burkina Faso, Togo, Benin, Nigeria, Cameroon, Equatorial Guinea, Gabon, Congo, Central African Republic, Angola, Democratic Republic of Congo, Uganda, western Kenya, northern Zambia)
  • P. d. figinii Storace, 1962Storace, L., 1962; Doriana 3 (129): 2 (highlands of Eritrea)
  • P. d. flavicornis Carpenter, 1947Carpenter, G.D.H. 1947 Proceedings of the Royal Entomological Society of London (B) 16: 55 (55-56) (Mt Kulal, north-western Kenya)
  • P. d. humbloti Oberthür, 1888Oberthür, C. 1888 Bulletin de la Société Entomologique de France (6) 8: XL (40-42) Full text (Comoro Islands)
  • P. d. meriones C. & R. Felder, 1865C. & R. Felder, 1865 . Reise der Österreichischen Fregatte Novara Wien, Bd 2 (Abth. 2) (1): 95 Full text (Madagascar)
  • P. d. meseres Carpenter, 1948 Carpenter, G. D. H., 1948 Proceedings of the Royal Entomological Society of London. (B) 17 (1-2): 14 (Uganda, south-western Kenya, Tanzania: the western, southern and south-eastern shores of Lake Victoria)
  • P. d. ochraceana Vane-Wright 1995 Vane-Wright, R. I., 1995 Carcasson's African Butterflies 144 (Mt. Marsabit, northern Kenya)
  • P. d. polytrophus Rothschild & Jordan, 1903Rothschild, W. & Jordan, K., 1903 Novitates Zoologicae 10 (3): 488 Full text (Kenya: highlands east of the Rift Valley)
  • P. d. sulfurea Palisot de Beauvois, 1806 Palisot de Beauvois, 1806 Insectes receueillis en Afrique et en Amérique 40 (276 pp.) Paris 46, pl. (São Tomé and Príncipe, Bioko)
  • P. d. tibullus Kirby, 1880 Kirby, W.F., 1880 Scientific Proceedings of the Royal Dublin Society 2: 339 (292-340). (eastern Kenya, eastern Tanzania, Malawi, Zambia)


Biogeographic realm
Afrotropical realm


Mimicry
The species shows polymorphism in appearance, though this is limited to females, which are often given as an example of in insects. This female-limited was first described in 1869 by . Males have a more or less uniform appearance throughout the species' range, but females come in at least 14 varieties or morphs.

Some female morphs share a very similar pattern of colouration with various species of distasteful butterfly (e.g. from the , a subfamily of ), while others have been found that mimic male appearance ( andromorphs). The persistence of these various morphs or different types of females may be explained by frequency-dependent selection. Cook et al. suggest that Batesian mimics gain a fitness advantage by avoiding predators, but suffer harassment from males (see ), whereas andromorphs (male mimics) are vulnerable to but are not harassed by male mating attempts.

Morphs are divided into three general groups based on patterning: the hippocoon group, the cenea group, and the planemoides group. The hippocoon group holds the largest amount of morphs; phenotypes within this group are characterized by four bands of alternating black and color patterns. Within the cenea group patterns are greatly dominated by black coloration and contain small splotches of color. The planemoides group has black bands surrounding the outside of the wing with a large splotch of color through the middle of the wing. This group also contains the female forms that are male-like mimics. Diversity in the wing patterns of each group is seen mostly in the coloration of each organism, while black patterns are generally consistent in each morph.

Phenotypic variation within the female morphs of Papilio dardanus has been found to be controlled at one locus named H that contains at least 11 different alleles. Recent studies have narrowed down the region of H to approximately 24 genes that is centered around the engrailed (en) gene which codes for specific transcription factors. The engrailed site has been found to have non-synonymous mutations throughout individuals in the species which would allow the divergence of each morph. Studies support that the engrailed gene in Papilio dardanus is monophyletic and has only evolved once within the species. Findings also suggest that the many different mimetic alleles in the Papilio dardanus genome are solely from mutations in the species. In other words, alleles did not enter into the genome from genetic transfer from other species.

Different combinations of the alleles at H lead to the variety of forms seen within the species. Genetic crosses of individuals found a general dominance hierarchy within the alleles. Allele combinations also determine not only which morph will be expressed but the actual size of the patterns shown. Each allele is able to either influence a larger or smaller mimetic pattern in an organism.

Such female-limited Batesian mimicry is not unique to this species, even in the genus . For instance shows a similar case of polymorphism in females. Similarly, male mimicry has been observed in another insect, a Ischnura ramburii which also appears to have evolved camouflage to avoid sexual coercion by males.Lessells, K. (2005). "Sexual Conflict". In Encyclopedia of Life Sciences.


See also
  • Disruptive selection
  • Phylogenetics of mimicry
  • , E. B. Ford and Philip Sheppard (some notable researchers)
  • mimetic model

==Gallery==

]]

  • Carcasson, R.H. (1960). "The Swallowtail Butterflies of East Africa (Lepidoptera, Papilionidae)". Journal of the East Africa Natural History Society pdf Key to East Africa members of the species group, diagnostic and other notes and figures. (Permission to host granted by The East Africa Natural History Society)
  • (1985). 9782880326036, IUCN. .


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