Great frigatebirds (Fregata minor) chasing a red-footed booby (Sula sula) to steal its food

Kleptoparasitism (originally spelt clepto-parasitism,[1][2] meaning "parasitism by theft") is a form of feeding in which one animal deliberately takes food from another. The strategy is evolutionarily stable when stealing is less costly than direct feeding, such as when food is scarce or when victims are abundant. Many kleptoparasites are arthropods, especially bees and wasps, but including some true flies, dung beetles, bugs, and spiders. Cuckoo bees are specialized kleptoparasites which lay their eggs either on the pollen masses made by other bees, or on the insect hosts of parasitoid wasps. They are an instance of Emery's rule, which states that insect social parasites tend to be closely related to their hosts. The behavior occurs, too, in vertebrates including birds such as skuas, which persistently chase other seabirds until they disgorge their food, and carnivorous mammals such as spotted hyenas and lions. Other species opportunistically indulge in kleptoparasitism.

Strategy

Kleptoparasitism is a feeding strategy where one animal deliberately steals food from another. This may be intraspecific, involving stealing from members of the same species, or interspecific, from members of other species.[3][4] The term denotes a form of parasitism involving theft, from Greek κλέπτω (kléptō, 'steal').[5] The strategy has been widely studied in birds; in four families, all seabirds, the Fregatidae, Chionididae, Stercoraridae, and Laridae, it occurs in more than a quarter of the species.[6][4]

Such a strategy should only be followed if it is evolutionarily stable, meaning that it offers a selective advantage to individuals that practise it. Kleptoparasitism costs time and energy which could otherwise be spent directly on feeding, so this cost must be outweighed by the benefit in energy gained from the stolen food. Mathematical modelling suggests that when food is abundant, ordinary feeding is the best strategy; when food abundance falls below a critical level, kleptoparasitism suddenly becomes advantageous, and aggressive interactions become common. Similarly, when potential victims are rare or widely dispersed, the time needed to find them may not be justified by the food that might be stolen from them, resulting in frequency-dependent selection.[3][6]

Taxonomic distribution

Arthropods

Bees and wasps

Cuckoo bee from the genus Nomada

There are many lineages of cuckoo bees, all of which lay their eggs in the nest cells of other bees, often within the same family.[7] Bombus bohemicus, for example, parasitises several other species in its genus, including B. terrestris, B. lucorum, and B. cryptarum.[8] These are instances of Emery's rule, named for the Italian entomologist Carlo Emery, which asserts that social parasites among insects, including kleptoparasites, tend to be closely related to their hosts.[9][10] The largest monophyletic lineage of kleptoparasitic bees is Nomadinae (a subfamily of Apidae), which comprises several hundred species in 35 genera.[11]

Some bees and their parasites[7]
Host genusParasite genus
BombusBombus (Psithyrus)
AnthophoraMelecta, Zacosmia
AmegillaThyreus
MegachileCoelioxys

The cuckoo wasps (Chrysididae) lay their eggs in the nests of potter and mud dauber wasps. Other families of wasps have "cuckoo" species that parasitise related species, as for example Polistes sulcifer, which parasitises a related species, P. dominula.[12][13] Numerous other wasp families have genera or larger lineages of which some or all members are kleptoparasitic (e.g., the genus Ceropales in Pompilidae and the tribe Nyssonini in Crabronidae).[7] Some of these species are inquilines and brood parasites rather than kleptoparasites.[14]

Others are dubbed kleptoparasitoids, namely parasitoids that select hosts that have been parasitized by another female. Kleptoparasitoids may make use of the punctures made by previous parasitoids on their hosts; may follow the trails or traces left by parasitoids to locate hosts; or use hosts already weakened by other parasitoids.[15]

Flies

Miltogrammine fly (Craticulina seriata) is a kleptoparasite of sand wasps, depositing its larvae on the food reserved for the larvae of the wasp

Some true flies (Diptera) are kleptoparasites; the strategy is especially common in the subfamily Miltogramminae of the family Sarcophagidae. There are also some kleptoparasites in the families Chloropidae and Milichiidae. Some adult milichiids, for example, visit spider webs where they scavenge on half-eaten stink bugs. Others are associated with robber flies (Asilidae), or Crematogaster ants.[16] Flies in the genus Bengalia (Calliphoridae) steal food and pupae transported by ants and are often found beside their foraging trails.[17] Musca albina (Muscidae) reportedly shows kleptoparasitic behaviour, laying eggs only in dung balls being interred by one of several co-occurring dung-rolling scarab species.[18]

Dung beetles

Scarab dung beetles relocate large amounts of vertebrate dung, rolling balls of the material to their nests for their larvae to feed on. Several smaller species of dung beetle do not gather dung themselves but take it from the nests of larger species. For example, species of Onthophagus enter dung-balls while Scarabeus beetles are making them.[19]

True bugs

Velia caprai (Ardennes, Belgium)

Many semiaquatic bugs (Heteroptera) are kleptoparasitic on their own species. In one study, whenever the bug Velia caprai (water cricket) took prey heavier than 7.9 g, other bugs of the same species joined it and successfully ate parts of the prey.[20]

Spiders

Kleptoparasitic spiders, which steal or feed on prey captured by other spiders, are known to occur in five families:

Vertebrates

Birds

A few bird species are specialist kleptoparasites, while many others are opportunistic. Skuas (including jaegers) and frigatebirds rely heavily on chasing other seabirds to obtain food. Other species—including raptors, gulls, terns, coots, and some ducks and shorebirds—do so opportunistically. Among opportunists such as the roseate tern, parent birds involved in kleptoparasitism are more successful in raising broods than non-kleptoparasitic individuals.[22][23] Bald eagles have been seen attacking smaller raptors, such as ospreys, to steal fish from them.[24] Among passerine birds, masked shrikes have been recorded stealing food from wheatears,[25] and Eurasian blackbirds have been recorded stealing smashed snails from other thrushes.[22]

During seabird nesting seasons, frigatebirds soar above seabird colonies, waiting for parent birds to return to their nests with food for their young. As the returning birds approach the colony, the frigatebirds, which are fast and agile, swoop in to pursue them vigorously; they sometimes seize tropicbirds by their long tail plumes. The name frigatebird, as well as many of the frigatebirds' colloquial names, including man-o'-war bird and pirate of the sea, denote this behaviour.[26] However, the amount of food obtained by kleptoparasitism in the magnificent frigatebird may be marginal.[27]

Gulls are both perpetrators and victims of opportunistic kleptoparasitism, particularly during the breeding season. While the victim is most often another member of the same species, other (principally smaller) gulls and terns can also be targeted. In the Americas, as brown pelicans surface and empty the water from their bills, they sometimes have their food stolen by Heermann's gulls and laughing gulls, which lurk nearby and grab escaping food items.[28] Great black-backed gulls are skilled kleptoparasites, stealing from other gulls and from raptors. Several species of gull steal food from humans, for example takeaway food at seaside resorts.[29]

Mammals

The relationship between spotted hyenas and lions, in which each species steals the other's kills,[30] is a form of kleptoparasitism.[20] Cheetahs are common targets. Bears, coyotes and wolves are very opportunistic and all have this behavior. All hyena species engage in this behavior when they can, as do jackals.[31] Human hunters may commonly take the remains of fresh kills from other carnivores, such as lions and Eurasian lynx.[32][33][34] Risso's dolphins have been observed charging "head-on" at sperm whales, causing them to open their mouths; it has been suggested that the observed harassment results in some regurgitation, and that the food is then eaten by the Risso's dolphins. The behaviour is rare and may be opportunistic.[35]

See also

References

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  2. Proffitt, M., ed. (1997). "kleptoparasitism". Oxford English Dictionary. Additions Series. Vol. 3. New York: Oxford University Press. p. 145. ISBN 978-0-19-860027-5.
  3. 1 2 Broom, Mark; Ruxton, Graeme D. (1998). "Evolutionarily stable stealing: game theory applied to kleptoparasitism". Annals of Human Genetics. 62 (5): 453–464. doi:10.1111/j.1469-1809.1998.ahg625_0453_5.x. S2CID 56407575.
  4. 1 2 Furness, R. W. (1987). "Kleptoparasitism in seabirds". In Croxall, J. P. (ed.). Seabirds: feeding ecology and role in marine ecosystems. Cambridge: Cambridge University Press. ISBN 978-0521301787.
  5. Nishimura, K. (2010). "Kleptoparasitism and Cannibalism". Encyclopedia of Animal Behavior. Elsevier. pp. 253–258. doi:10.1016/b978-0-08-045337-8.00279-5. ISBN 9780080453378.
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  7. 1 2 3 Slater, Peter J. B.; Rosenblatt, Jay S.; Snowdon, Charles T.; et al. (30 January 2005). Advances in the Study of Behavior. Academic Press. p. 365. ISBN 978-0-08-049015-1.
  8. Kreuter, Kirsten; Bunk, Elfi Bunk (2011). "How the social parasitic bumblebee Bombus bohemicus sneaks into power of reproduction". Behavioral Ecology and Sociobiology. 66 (3): 475–486. doi:10.1007/s00265-011-1294-z. S2CID 7124725.
  9. Deslippe, Richard (2010). "Social Parasitism in Ants". Nature Education Knowledge. Retrieved 25 May 2022.
  10. Emery, Carlo (1909). "Über den Ursprung der dulotischen, parasitischen und myrmekophilen Ameisen" [On the Origin of Dulotic, Parasitic, and Myrmecophilic Ants]. Biologisches Centralblatt (in German). 29: 352–362.
  11. Roig-Alsina, A. (1991). "Cladistic analysis of the Nomadinae s. str. with description of a new genus (Hymenoptera: Anthophoridae)". Journal of the Kansas Entomological Society. 64 (1): 23–37. JSTOR 25085241.
  12. Dapporto, L.; Cervo, R.; Sledge, M.F.; Turillazzi, S. (2004). "Rank integration in dominance hierarchies of host colonies by the paper wasp social parasite Polistes sulcifer (Hymenoptera, Vespidae)". Journal of Insect Physiology. Elsevier BV. 50 (2–3): 217–223. doi:10.1016/j.jinsphys.2003.11.012. PMID 15019524.
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  16. Wild, A.L. & Brake, I. 2009. Field observations on Milichia patrizii ant-mugging flies (Diptera: Milichiidae: Milichiinae) in KwaZulu-Natal, South Africa. African Invertebrates 50 (1): 205–212. Archived 2009-05-15 at the Wayback Machine
  17. Sivinski, J., S. Marshall and E. Petersson (1999) Kleptoparasitism and phoresy in the diptera. Florida Entomologist 82 (2) Archived 2008-09-10 at the Wayback Machine
  18. Marshall, S.A. & Pont, A.C. (2013). The kleptoparasitic habits of Musca albina Wiedemann, 1830 (Diptera: Muscidae). African Invertebrates 54(2): 427–430.
  19. Hammond, P. M. (September 1976). "Kleptoparasitic Behaviour of Onthophagus suturalis Peringuey (Coleoptera: Scarabaeidae) and Other Dung-Beetles". The Coleopterists Bulletin. 30 (3): 245–249. JSTOR 3999694.
  20. 1 2 Erlandsson, Ann (1988). "Food sharing vs monopolising prey: a form of kleptoparasitism in Velia caprai (Heteroptera)". Oikos. 53 (2): 203–206. doi:10.2307/3566063. JSTOR 3566063.
  21. Coyl, F. A.; O'Shields, T. C.; Perlmutter, D. G. (1991). "Observations on the behaviour of the kleptoparasitic spider, Mysmenopsis furtiva (Araneae, Mysmenidae)" (PDF). Journal of Arachnology. 19: 62–66. Archived from the original (PDF) on 2006-05-13. Retrieved 2006-07-11.
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  34. Krofel, Miha; Kos, Ivan; Linnell, John; Odden, John; Teurlings, Ivonne (2008). "Human Kleptoparasitism on Eurasian Lynx (Lynx Lynx L.) in Slovenia and Norway" (PDF). Varstvo Narave. 21: 93–103. Archived from the original (PDF) on 2022-06-16. Retrieved 2022-05-25.
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