Papilio xuthus

Papilio xuthus, the Asian swallowtail, Chinese yellow swallowtail or Xuthus swallowtail, is a yellow-colored, medium to large sized swallowtail butterfly found in northeast Asia, northern Myanmar, southern China, Taiwan, the Korean Peninsula, Japan (from Hokkaidō to the Yaeyama Islands), Siberia and the Hawaiian Islands.[1] It was also recorded in the state of Arunachal Pradesh, India, in 2014.[2]

"Asian swallowtail" redirects here. For the other butterfly with this common name, see Papilio lowi.

Asian swallowtail
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Lepidoptera
Family: Papilionidae
Genus: Papilio
Species:
P. xuthus
Binomial name
Papilio xuthus
Linnaeus, 1767

It mates multiple times in its life, leading to an increased genetic diversity in its young.[3] It is preyed upon by a host of organisms, including the tree cricket Oecanthus longicauda, ant Lasius niger, and wasps (Polistes and Trogus mactator).[4] P. xuthus utilizes color vision and color constancy while foraging for plants of the family Rutaceae.[5]

It is common and not threatened.[1] Papilio xuthus is common in urban, suburban, woods and orange orchards. The flight period is from May to August.[6]

Males use both physical and visual cues to attract mates during the breeding season. Females of the species regularly mate with multiple partners. After mating, females use habitat and food quality to determine where they will oviposit their eggs.

Taxonomy

Papilio xuthus is a member of the genus Papilio. It is of the family Papilionidae and order Lepidoptera.[7] It was first introduced in Hawaii in 1971 from Japan or Guam.[8] P. xuthus makes significant seasonal migrations over 200 km.[9] There are three subspecies of P. xuthus: Papilio xuthus xuthus, Papilio xuthus koxinga,[10] and Papilio xuthus neoxuthus.[6]

Description

The Asian swallowtail is a mid-sized, yellow, prominently-tailed butterfly.[11] It has a wingspan of 90 to 110 mm.[11] Its normal color pattern consists of a black pattern on a yellow background.[11] Wing coloration is sexually dimorphic, with females showing broader proximal marginal bands in the hindwing.[11] Blue-iridescent and orange scales separate the black bands on the hindwing.[11] The black bands also run in stripes of varying thickness along the forewing.[11] The young caterpillar mimics bird feces and has a white and brown spot on its head.[6] As they mature, caterpillars develop a light green body color with brown spots.[6]

Wing coloration

P. xuthus have highly sensitive photoreceptors, or ommatidia, that can detect a wide range of wavelengths.[12] This adaptation helps them identify members of their own species. Their distinct coloring and patterning are what sets them apart from other butterflies. Wing color is derived from "scales", and P. xuthus has scales of yellow (cream), orange, black, and blue from the light each scale absorbs and reflects. Spectrophotometer studies saw that the yellow scales absorbed in the UV to violet range, orange absorbed in the lower half-wavelengths of the visible spectrum, black scales absorbed in most of the visible light range, and blue scales absorbed very little light. These absorbance ranges are due to the pigment molecules contained in each wing scale. Yellow and orange contain papiliochrome II and black contains melanin. The blue scales are unique in that they don't have a pigment molecule, and are instead colored by an optical phenomenon. The interaction of light with the upper and lower lamina of the scale gives them the distinct blue color that we see.[12]

Experimental manipulation of wing coloration has been achieved through administration of the acid carboxypeptidase, Molsin. Injection of Molsin into 0-2 day pupae, butterflies had high amounts of black wing scales. These modified subjects had produced high amounts of melanin and papiliochrome II. Injection of Molsin into 3-4 day pupae shows no change in wing coloration. This indicates that P. xuthus likely has an acid carboxypeptidase of its own that naturally induces production of these pigments, and its action lasts during the first two days of pupation. Administration of a higher amount of acid carboxypeptidase to the pupae at 0–2 days induces an overproduction of pigmentation molecules, which leads to a high number of black scales.[13]

P. xuthus uses wing coloration and patterning to identify insects of the same species. Sexual behaviors are elicited from males by visual identification alone. Adult P. xuthus males were able to find odorless conspecifics, and while they do not discriminate by sex, they can identify a female once physical contact is made.[14]

Courtship and mating

During the mating season, Asian swallowtail males fly through the foliage of trees in search of a mate.[15] If a male encounters a female resting on a plant with open and horizontal wings, it approaches her and examines her by contacting his forelegs with the tips of her wings.[15] In addition, males use visual cues to conduct the mating ritual and are particularly attracted to closely spaced yellow patches on female wings.[15]

Most females of the Asian swallowtail butterfly mate more than once in their life. This behavior is typical of many other swallowtail butterflies including P. glaucus, P. helenus and P. protenor.[3][16][17] Multiple matings leads to an increased genetic diversity of swallowtail offspring.[18] In addition, multiple matings allow females to produce a greater number of eggs, of which there can be up to thirty.[19]

Oviposition

Female butterflies disperse when they are about to oviposit. They decide on the number of eggs they deposit in different subhabitats by certain criteria such as the quality of the subhabitat, the existing adult population in the area, the quantity of young leaves in the vicinity, the degree of sun exposure (females prefer sunnier areas),[20][21] and host plant height.[4]

Mortality factors
P. xuthus larva - upper: osmeterium everted - lower: undisturbed

Predation

Some insects, such as the grasshopper Oeanthus longicauda, are capable of removing Asian swallowtail larvae out of their eggs before they hatch.[4] During the first and second larval instars, their main predators are ants (particularly Lasius niger), spiders, and various other bugs.[4]

Asian swallowtail caterpillars may also be parasitized by wasps, such as Trogus mactator and Pteromarus puparum, during development. These wasps ultimately kill the larvae after pupation.[4] In fact, wasps have been observed emerging from the host pupa four or five days after the predicted date of emergence of the host.[4]

Environment

Aside from predation, larval mortality rate is also affected by diseases that appear to correlate with the duration of the rainy season.[4] Long days of rain in autumn lead to the rotting of infected larvae.[4]

Foraging

Asian swallowtail butterflies exhibit color vision which gives them the ability to differentiate objects of contrasting colors irrespective of brightness.[5] They also exhibit color constancy, which allows them to recognize the color of an organism regardless of the background light.[5] Asian swallowtail butterflies show this color constancy even when the background light is yellow and red.[5] This ability is important for foraging, as it allows butterflies to recognize certain flowers in an area irrespective of whether the flower is in the shade or in the sun.[5]

Food plants

The larvae of the species feed on plants of family Rutaceae. Recorded species of food plants include:

Development and population dynamics

Despite its wide distribution, populations of the Asian swallowtail remain at a stable, relatively low, level. There are typically four to five generations per year with the adults of the first generation emerging from mid-April to early May and adults of the second generation emerging in mid-June.[20][23] P. xuthus will lay single eggs on leaves of host plants, allowing hatched larvae to feed on Poncirus trifoliata, Zanthoxylum ailanthoides and various citrus species.[4] The larval stage lasts for approximately three to five weeks while the pupal stage is around two weeks.[4]

According to a study, the population fluctuation of the Asian swallowtail butterfly has been surprisingly stable compared to that of various other insects.[20] The stability of the population appeared to be regulated by the population dynamics of egg the parasitoids, Trichogramma, and the pupal parasitoids, Pteromalus puparum, which maintained shorter life spans and generation times than the eggs of the Asian swallowtail.[20] When the butterfly population reaches a high density, because of the shorter generational turn around of the parasites, intergeneration responses of the parasites are faster than those of the butterflies, resulting in a responding increased growth of the parasites.[20] This creates an evolutionary stable system to keep the population of both the parasites and the host in check.[20] It was also found that among the subpopulations studied, exchanges between each subpopulation helped to maintain the stability of the entire population as a whole.[20]

See also
Wikimedia Commons has media related to Papilio xuthus.

References
  1. Collins, N. Mark; Morris, Michael G. (1985). "Papilio (Princeps) xuthus (Linnaeus, 1760)". Threatened Swallowtail Butterflies of the World: The IUCN Red Data Book. Gland & Cambridge: IUCN. p. 95. ISBN 978-2-88032-603-6 – via Biodiversity Heritage Library.
  2. Kunte, K.; P. Roy; S. Kalesh; U. Kodandaramaiah, eds. (2016). "Papilio xuthus Linnaeus, 1767 – Asian Yellow Swallowtail". Butterflies of India, v. 2.24. Indian Foundation for Butterflies. Retrieved 10 August 2016.
  3. Watanabe, M., and Nozato, K. (1986). Fecundity of the yellow swallowtail butterflies,Papilio xuthus and P. machaon hippocrates, in a wild environment.Zool. Sci. 3: 509–515.
  4. Watanabe, Mamoru (March 1976). "A preliminary study on population dynamics of the swallowtail butterfly,Papilio xuthus L. In a deforested area". Researches on Population Ecology. 17 (2): 200–210. doi:10.1007/BF02530771. S2CID 33092266.
  5. Kinoshita, Michiyo; Kentaro Arikawa (2000). "Color Constancy of the Swallowtail Butterfly, Papilio xuthus". The Journal of Experimental Biology. 203 (Pt 23): 3521–3530. doi:10.1242/jeb.203.23.3521. PMID 11060214. Retrieved 25 October 2013.
  6. "Papilio xuthus (Asian Swallowtail, Japanischer Schwalbenschwanz, Machaon asiatique)". Archived from the original on 23 February 2018. Retrieved 20 November 2013.
  7. Roskov Y., Kunze T., Paglinawan L., Orrell T., Nicolson D., Culham A., Bailly N., Kirk P., Bourgoin T., Baillargeon G., Hernandez F., De Wever A., eds (2013). Species 2000 & ITIS Catalogue of Life, 2013 Annual Checklist. Digital resource at www.catalogueoflife.org/annual-checklist/2013/. Species 2000: Reading, UK.
  8. Scott, J. A. 1986. The butterflies of North America. Stanford University Press.
  9. NatureServe (2013). "NatureServe Explorer: An online encyclopedia of life [web application]: Papilio xuthus - Linnaeus, 1767". Virginia: NatureServe. Retrieved 20 November 2013.
  10. Fruhstorfer, H. (1908). "Lepidopterisches Pêle-Mêle. I. Neue ostasiatische Rhopaloceren". Entomologische Zeitschrift. 22 (11): 46–47.
  11. Koch; Nijhout (2002). "The Role of Wing Veins in Colour Pattern Development in the Butterfly, Papilio xuthus". European Journal of Entomology. 99: 67–72. doi:10.14411/eje.2002.012.
  12. Stavenga, Doekele G; Matsushita, Atsuko; Arikawa, Kentaro (2015). "Combined pigmentary and structural effects tune wing scale coloration to color vision in the swallowtail butterfly Papilio xuthus". Zoological Letters. 1: 14. doi:10.1186/s40851-015-0015-2. ISSN 2056-306X. PMC 4657377. PMID 26605059.
  13. Osanai, Minoru; Umebachi, Yoshishige (2003). "Perturbation of the Wing Color Pattern of a Swallowtail Butterfly, Papilio xuthus, Induced by Acid Carboxypeptidase". Zoological Science. 20 (3): 325–331. doi:10.2108/zsj.20.325. ISSN 0289-0003. PMID 12692391. S2CID 25029765.
  14. Yamashita, Keiko; Hidaka, Toshitaka (25 December 1975). "Wing Color Pattern as the Releaser of Mating Behavior in the Swallowtail Butterfly, Papilio xuthus L.(Lepidoptera : Papilionidae)". Applied Entomology and Zoology. 10 (4): 263–267. doi:10.1303/aez.10.263. ISSN 0003-6862.
  15. Hidaka, Toshitaka; Keiko Yamashita (December 1975). "Wing Color Pattern as the Releaser of Mating Behavior in the Swallowtail Butterfly, Papilio xuthus L. (Lepidoptera: Papilionidae)". Applied Entomology and Zoology. 10 (4): 263–267. doi:10.1303/aez.10.263.
  16. Watanabe, M., Nozato, K., and Kiritani, K. (1986). Studies on ecology and behavior of Japanese black swallowtail butterflies. V. Fecundity in summer generations.Appl. Entomol. Zool. 21: 448–453.
  17. Burns, J. M. (1966). Preferential mating versus mimicry: Disruptive selection and sex-limited dimorphism in Papilio glaucus.Science 153: 551–553.
  18. Walker, W. F. (1980). Sperm utilization strategies in nonsocial insects.Am. Nat. 115: 780–799.
  19. Watanabe, Mamoru (1988). "Multiple matings increase the fecundity of the yellow swallowtail butterfly,Papilio xuthus L., in summer generations". Journal of Insect Behavior. 1 (1): 17–29. doi:10.1007/BF01052501. S2CID 30702862.
  20. Hirose, Y.; Y. Suzuki; M.Takagi; K. Hiehata; M. Yamasaki; H. Kimoto; M. Yamanaka; M. Iga; K. Yamaguchi (March 1980). "Population dynamics of the citrus swallowtail,Papilio xuthus Linné (Lepidoptera: Papilionidae): Mechanisms stabilizing its numbers". Researches on Population Ecology. 21 (2): 260–285. doi:10.1007/BF02513625. S2CID 3120811.
  21. Suzuki, Y., K. Yamaguchi, M. Iga, Y. Hirose and H. Kimoto (1976) Spatial distribution of the eggs of Papilio xuthus Linné (Lepidoptera: Papilionidae) in a citrus grove.Jap. J. appl. Ent. Zool. 20: 177–183. (In Japanese with English synopsis),
  22. Savela, Markku (16 February 2008). "Papilio". Lepidoptera and some other life forms. nic.funet.fi. Retrieved 9 November 2010.
  23. Inaba, S. (1937) The ecological observation on the swallowtail butterflyPapilio xuthus L. (II).Acta Zooecologica 1, (2): 17–29.
  • Harry, J. L. 1994. Papilio xuthus in Hawaii: A Photo Life History (Lepidoptera: Papilionidae). Tropical Lepidoptera 5(1): 6–7. pdf
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