Mud-puddling

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Mud-puddling is the phenomenon mostly seen in butterflies and involves their aggregation on substrates like wet soil, dung and carrion to obtain nutrients such as salts and amino acids.[1] This behaviour has also been seen in some other insects, notably the leafhoppers.[2]

Lepidoptera (butterflies and moths) are diverse in their strategies to gather liquid nutrients. Typically, mud-puddling behavior takes place on wet soil. But even sweat on human skin may be attractive to butterflies.[3] The most unusual sources include blood and tears (see below).

This behaviour is restricted to males in many species, and in some like Battus philenor the presence of an assembly of butterflies on the ground acts as a stimulus to join the presumptive mud-puddling flock.[4]

Contents

[edit] Mud-puddling on soil

Spot Swordtail (Graphium (Pathysa) nomius) excreting excess water after mud-puddling
Spot Swordtail (Graphium (Pathysa) nomius) excreting excess water after mud-puddling

In tropical India this phenomenon is mostly seen in the post-monsoon season. The groups can include several species often including members of the Papilionidae and Pieridae.[5]

Males seem to benefit from the sodium uptake through mud-puddling behaviour with an increase in reproductive success. The collected sodium and amino acids are often transferred to the female with the spermatophore during mating as a nuptial gift. This nutrition also enhances the survival rate of the eggs.[6]

When puddling many butterflies and moths pump fluid through the digestive tract and release fluid from their anus. In some species such as the male Notodontid Gluphisia septentrionis this is released in forced anal jets at 3 second intervals. Fluid of up to 600 times the body mass may pass through and males have a much longer ileum (anterior hindgut) than non-puddling females.[7]

[edit] Other sources of liquid nutrients

Those species that are attracted to dung (e.g. Zeuxidia spp.) or carrion seem to be prefer ammonium ions rather than sodium.[8] By rotting, fruits make available to butterflies sugars and their derivatives such as alcohols, which are mainly useful as carbohydrate "fuel" for ATP production.[9]

In Borneo lowland rain forest, numerous species of butterflies regularly visit decaying fruit to drink. This behavior is mainly opportunistic, though some are highly attracted to old fruit, notably Satyrinae (e.g. Neorina lowii) and Limenitidinae such as Bassarona dunya.[10]

Carrion is usually more intentionally utilized. Carrion-feeders seem to represent a different feeding guild from "classical" mud-puddlers and fruit-feeders. They include diverse taxa like the brush-footed butterflies Cirrochroa emalea (Nymphalinae) and Charaxes bernardus (Tawny Rajah, Charaxinae), and Lycaenidae like Curetis tagalica and Cheritra freja.[10]

Blue Lesser Purple Emperor (Apatura ilia f. ilia) on dung
Blue Lesser Purple Emperor (Apatura ilia f. ilia) on dung

It seems that carrion-feeding evolves often in some lineages and is highly convergent overall. Dedicated carrion-feeders may even have the ability to smell out and home in on rotting meat over hundreds of meters. In the Bornean Charaxinae, dedicated (Charaxes bernardus) or opportunistic (some other Charaxes and Polyura) tend to have a markedly larger bulk and smaller wings, making them more dashing, maneuvrable flyers than fruit specialists like Prothoe franck and opportunistic fruit visitors such as Charaxes durnfordi. Other butterflies like most Pieridae, Papilionidae and Morphinae are rarely if ever seen on carrion, dung and rotting fruit, though they may be avid mud-puddlers in the strict sense. Altogether, the Nymphalidae show the highest variety of nutrient-gathering strategies among the butterflies; the Limenitidinae have numerous mud-puddlers that also frequently visit dung but avoid fruits and carrion (namely the genus Limenitis),[10] and some which are attracted to any pungent substance.[11]

Certain moths, mainly of the subfamily Calpinae, are somewhat notorious for their blood- and tear-drinking habits. Hemiceratoides hieroglyphica of Madagascar has been noted to visit and suck tears by inserting their proboscis into the closed eyelids of roosting birds.[12] Some species of the genus Calyptra are called "vampire moths" as they suck blood from sleeping vertebrates, including humans. Ophthalmotropy (= eye-attraction) or lachryphagy (= tear drinking) is noted in a number of unrelated moths which visit mammals.[13]

[edit] See also

[edit] Footnotes

  1. ^ Beck et al. (1999)
  2. ^ E.g. potato leafhopper, Empoasca fabae: Adler (1982)
  3. ^ E.g. Halpe spp.: Collenette (1934), Hamer et al. (2006)
  4. ^ Collenette (1934), Sculley & Boggs (1996), Locke et al. (2003), Hamer et al. (2006)
  5. ^ Sreekumar & Balakrishnan (2001)
  6. ^ Pivnik & McNeil (1987), Medley & Eisner (1996), Molleman et al. (2004)
  7. ^ Scott R. Smedley in Resh, V. H. & R. T. Cardé (Editors) 2003. Encyclopedia of Insects. Academic Press.
  8. ^ Erhardt & Rusterholz (1998)
  9. ^ DeVries & Walla (2001)
  10. ^ a b c Hamer et al. (2006)
  11. ^ Several Apatura species are famous among lepidopterologists for being easily attracted with stinking cheese.
  12. ^ Hilgartner et al (2007)
  13. ^ Notably Mecistoptera griseifusa; see also Bänziger (1992).

[edit] References

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  • Adler, P.H. (1982): Nocturnal occurrences of leafhoppers (Homoptera: Cicadellidae) at soil. Journal of the Kansas Entomological Society 55(1): 73–74. HTML abstract
  • Bänziger, H. (1992): Remarkable new cases of moths drinking human tears in Thailand (Lepidoptera: Thyatiridae, Sphingidae, Notodontidae). Natural History Bulletin of the Siam Society 40: 101–102.
  • Beck, J.; Mühlenberg, E. & Fiedler, K. (1999): Mud-puddling behavior in tropical butterflies: In search of proteins or minerals? Oecologia 119(1): 140–148. doi:10.1007/s004420050770 (HTML abstract)
  • Collenette, C.L. (1934): On the sexes of some South American moths attracted to light, human perspiration and damp sand. Entomologist 102: 769-791.[verification needed]
  • DeVries, P.J. & Walla, T.R. (2001): Species diversity and community structure in neotropical fruit-feeding butterflies. Biol. J. Linn. Soc. 74: 1–15. PDF fulltext
  • Erhardt, A. & Rusterholz, H.P. (1998): Do Peacock butterflies (Inachis io) detect and prefer nectar amino acids and other nitrogenous compounds? Oecologia 117(4): 536-542. doi:10.1007/s004420050690 (HTML abstract)
  • Hamer, K.C.; Hill, J.K.; Benedick, S.; Mustaffa, N.; Chey, V.K. & Maryati, M. (2006): Diversity and ecology of carrion- and fruit-feeding butterflies in Bornean rain forest. Journal of Tropical Ecology 22(1): 25–33. doi:10.1017/S0266467405002750 (HTML abstract)
  • Hilgartner, R.; Raoilison, Mamisolo; Büttiker, Willhelm; Lees, David C. & Krenn, Harald W. (2007): Malagasy birds as hosts for eye-frequenting moths. Biol. Lett. 3(2): 117–120. doi:10.1098/rsbl.2006.0581 (HTML abstract)
  • Locke, B.; Otis, Gard W.; McKenzie, Nicole G.; Cheung, D.; MacLeod, E.C. & Kwoon, A. (2003): Mud puddling Papilio and Battus swallowtail butterflies (Papilionidae) have different mechanisms for social facilitation. 2003 Entomological Society of America Annual Meeting Poster Presentation D0541. HTML abstract
  • Medley S.R. & Eisner, T. (1996): Sodium: a male nuptial gift to its offspring. PNAS 93(2): 809–813. PDF fulltext
  • Molleman, F.; Zwaan, B.J. & Brakefield, P.M. (2004): The effect of male sodium diet and mating history on female reproduction in the puddling squinting bush brown Bicyclus anynana (Lepidoptera). Behavioral Ecology and Sociobiology 56(4): 404–411. doi:10.1007/s00265-004-0789-2 (HTML abstract)
  • Pivnik, K. & McNeil, J.N. (1987): Puddling in butterflies: sodium affects reproductive success in Thymelicus lineola. Physiological Entomology 12(4): 461–472.
  • Sculley, C.E. & Boggs, C.L. (1996): Mating systems and sexual division of foraging effort affect puddling behaviour by butterflies. Ecological Entomology 21(2): 193-197. PDF fulltext
  • Sreekumar, P.G. & Balakrishnan, M. (2001): Habitat and altitude preferences of butterflies in Aralam Wildlife Sanctuary, Kerala. Tropical Ecology 42(2): 277-281. PDF fulltext