Papilio dardanus

Papilio dardanus
Dorsal view
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Family: Papilionidae
Genus: Papilio
Species: P. dardanus
Binomial name
Papilio dardanus
Brown, 1776[1]
Subspecies

See text

Synonyms

Papilio dardanus, the African swallowtail, mocker swallowtail or flying handkerchief, is a species of butterfly in the family Papilionidae (the swallowtails). The species is broadly distributed throughout Sub-Saharan Africa.[2] The British entomologist E. B. Poulton described it as "the most interesting butterfly in the world".[3]

Classification

Molecular studies have provided evidence that this species' closest relative is Papilio phorcas, with Papilio constantinus being the next closest (see images below).[4] It is a member of the Papilio genus of which Papilio appalachiensis and Papilio xuthus are also members.

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

Subspecies

Listed alphabetically:[5]

Ecozone

Afrotropic ecozone

Mimicry

Mating

The species shows polymorphism in wing appearance, though this is limited to females, which are often given as an example of Batesian mimicry in insects. This female-limited mimicry was first described in 1869 by Roland Trimen.[6] Males have a more or less uniform appearance throughout the species' range, but females come in at least 14 varieties or morphs.[2]

Some female morphs share a very similar pattern of colouration with various species of distasteful butterfly (e.g. from the Danainae, a subfamily of nymphalids),[7] 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 sexual conflict), whereas andromorphs (male mimics) are vulnerable to predation but are not harassed by male mating attempts.[8]

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.[2]

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.[2] 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.[9] The engrailed site has been found to have non-synonymous mutations throughout individuals in the species which would allow the divergence of each morph.[9] Studies support that the engrailed gene in Papilio dardanus is monophyletic and has only evolved once within the species.[10] 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.[10]

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.[2] 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.[2]

Such female-limited Batesian mimicry is not unique to this species, even in the genus Papilio. For instance Papilio memnon shows a similar case of polymorphism in females.[11] Similarly, male mimicry has been observed in another insect, a damselfly Ischnura ramburii which also appears to have evolved camouflage to avoid sexual coercion by males.[12]

See also

References

  1. Peter Brown, 1776 . Nouvelles illustrations de zoologie, contenant cinquante planches enluminées d'oiseaux curieux, et qui non etés jamais descrits, et quelques de quadrupedes, de reptiles et d'insectes, avec de courtes descriptions systematiques. - New illustrations of zoology, containing fifty coloured plates of new, curious, and non-descript birds, with a few quadrupeds, reptiles and insects. Together with a short and scientific description of the same London. (White).
  2. 1 2 3 4 5 6 Nijhout, H. F. (2003). "Polymorphic mimicry in Papilio dardanus: mosaic dominance, big effects, and origins" (PDF). Evolution and Development. 5 (6): 579–592. doi:10.1046/j.1525-142X.2003.03063.x. PMID 14984040. Retrieved 2009-08-22.
  3. Poulton, E. B. (1924). "Papilio dardanus. The most interesting butterfly in the world". Journal of the East African and Ugandan Natural History Society. 20: 4–22.
  4. Vane-Wright, R. I.; Raheem, D. C.; Cieslak, A.; Vogler, A. P. (1999). "Evolution of the mimetic African swallowtail butterfly Papilio dardanus: molecular data confirm relationships with P. phorcas and P. constantinus". Biological Journal of the Linnean Society. 99: 215–229. doi:10.1111/j.1095-8312.1999.tb01885.x.
  5. Papilio, funet.fi
  6. Trimen, R. (1869). "On some remarkable mimetic analogies among African butterflies". Transactions of the Linnean Society of London. 26 (3): 497–522. doi:10.1111/j.1096-3642.1869.tb00538.x.
  7. Mallet, J. (2001). "Batesian mimicry in Papilio dardanus". Retrieved 2009-08-23.
  8. Cook, S. E.; Vernon, J. G.; Bateson; M., Guilford, T. (1994). "Mate choice in the polymorphic African swallowtail butterfly, Papilio dardanus: Male-like females may avoid sexual harassment". Animal Behaviour. 47 (2): 389–397. doi:10.1006/anbe.1994.1053.
  9. 1 2 Timmermans, M. J. T. M.; Baxter, S. W.; Clark, R.; Heckel, D. G.; Vogel, H.; Collins, S.; Papanicolaou, A.; Fukova, I.; Joron, M.; Thompson, M. J.; Jiggins, C. D.; ffrench-Constant, R. H.; Vogler, A. P. (2014). "Comparative genomics of the mimicry switch in Papilio dardanus". Proceedings of the Royal Society: Biological Sciences. 281. doi:10.1098/rspb.2014.0465.
  10. 1 2 Thompson, M. J.; Timmermans, M. J. T. N.; Jiggins, C. D.; Vogler, A. P (2014). "The evolutionary genetics of highly divergent alleles of the mimicry locus in Papilio dardanus". BMC Evolutionary Biology. 14. doi:10.1186/1471-2148-14-140.
  11. Mallet, James (2001). "Batesian mimicry in Papilio memnon". Retrieved 2009-09-09.
  12. Lessells, K. (2005). "Sexual Conflict". In Encyclopedia of Life Sciences.
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