Mobbing behavior

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The Great Tit, a passerine bird, employs both mobbing behavior and alarm calls.
The Great Tit, a passerine bird, employs both mobbing behavior and alarm calls.

In behavioral ecology, mobbing behavior is an antipredator behavior which occurs when individuals of a certain species mob a predator by cooperatively attacking or harassing it, usually in order to protect their offspring. A simple definition of mobbing is an assemblage of individuals around a potentially dangerous predator.[1] This is most frequently seen in avian species, though it is also known to occur in other social animals. While mobbing has evolved independently in many species, it only tends to be present in those whose young are frequently preyed on. This behavior may complement cryptic adaptations in the offspring themselves, such as camouflage and hiding. Mobbing calls may be used to summon nearby individuals to cooperate in the attack.

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[edit] Mobbing in birds

Nesting Kittiwakes.
Nesting Kittiwakes.
Crow mobbing perched Bald Eagle
Crow mobbing perched Bald Eagle
One second later
One second later
"Dive-bombing"
"Dive-bombing"

Birds that breed in colonies such as gulls are widely seen to attack intruders, including encroaching humans.[2] Behavior includes flying about the intruder, dive bombing, loud squawking and defecating on the predator. Costs of mobbing behavior include the risk of engaging with predators, as well as energy expended in the process. Black-headed Gulls are one species which aggressively engages intruding predators, such as Carrion Crows. Classic experiments on this species by Hans Kruuk involved placing hen eggs at intervals from a nesting colony, and recording the percentage of successful predation events as well as the probability of the crow being subjected to mobbing.[3] The results showed decreasing mobbing with increased distance from the nest, which was correlated with increased predation success. Mobbing may function by reducing the predator's ability to locate nests, in other words as a distraction, since predators cannot focus on locating eggs while they are under direct attack.

Adaptationist hypotheses regarding why an organism should engage in such risky behavior have been suggested by Eberhard Curio,[4] including advertising their physical fitness and hence uncatchability (much like stotting behavior in gazelles), distracting predators from finding their offspring, warning their offspring, luring the predator away, allowing offspring to learn to recognize the predator species,[5] directly injuring the predator or attracting a predator of the predator itself. The much lower frequency of attacks between nesting seasons suggests such behavior may have evolved due to its benefit for the mobber's young. Niko Tinbergen argued that the mobbing was a source of confusion to gull chick predators, distracting them from searching for prey .[6] Indeed, an intruding carrion crow can only avoid incoming attacks by facing its attackers, which prevents it from locating its target.[2]

Besides experimental research, the comparative method can also be employed to investigate hypotheses such as those given by Curio above. For example, closely related species such as the Kittiwake do not show mobbing behavior. The kittiwake's cliff nests are almost completely inaccessible to possible predators due to gusty winds and the sheer cliffs they nest in, meaning its young are not at risk to predation like the Black-headed Gull.[7] This is an example of an evolutionary pattern known as divergent evolution.

Mobbing is thought to carry risks to roosting predators, including suffering harm from the mobbing birds or the risk of attracting larger, more dangerous predators. Birds at risk of mobbing such as owls have adapted cryptic plumage and hidden roosting sites in order to reduce this danger.[8]

[edit] In other animals

The occurrence of mobbing behavior across widely different taxa, including California Ground Squirrels, is evidence of convergent evolution.
The occurrence of mobbing behavior across widely different taxa, including California Ground Squirrels, is evidence of convergent evolution.

Another way the comparative method can be used here is by comparing gulls with distantly related organisms. This approach relies on the existence of convergent evolution, where distantly related organisms evolve the same trait due to similar selection pressures. As mentioned, many bird species such as the swallows also show mobbing of predators, however even more distantly related species including mammals are known to engage in this behavior. One example is California Ground Squirrels, which are known to distract predators such as the rattlesnake and gopher snake from locating their nest burrows by kicking sand into their eyes.[9] This social species also uses alarm calls.

Mobbing has also been observed in fishes, for example bluegills have been seen to attack snapping turtles.[1] Bluegills, which form large nesting colonies, were seen to attack both released and naturally occurring turtles, which may function to advertise their presence, drive the predator from the area, or aid in cultural transmission of predator recognition.

[edit] Mobbing calls

Mobbing calls are signals made by the mobbing species while harassing a predator. These differ from alarm calls, which allow con-specifics to escape from the predator. The Great Tit, a European songbird uses such a signal to call on nearby birds to harass a perched bird of prey, such as an owl. This call occurs in the 4.5kHz range,[2] and is effective in traveling long distances. However, when their prey are in flight, they employ an alarm signal in the 7-8kHz range. This call is less effective at travelling great distances, but is much more difficult for both owls and hawks to hear (and detect the direction from which the call came).[10] In the case of the alarm call, it is disadvantageous to the sender if the predator picks up on the signal, hence selection has favored those birds able to hear and employ calls in this higher frequency range.

Mobbing calls may also be part of an animal's arsenal in harassing the predator - for example studies of Phainopepla mobbing calls indicate it may serve to enhance the swooping attack on the predators, including Scrub Jays. In this species the mobbing call is smoothly upsweeping, and is made when swooping down in an arc beside the predator. This call was also heard during agonistic interactions with conspecifics, and may serve additionally or alternatively as an alarm call to their mate.[11]

[edit] Evolution

The evolution of mobbing behaviour is explained using evolutionary stable strategies which are in turn based on Game Theory.[12]

Mobbing involves risks (costs) to the individual and benefits (payoffs) to the individual and others. The individuals themselves are often genetically related and it is increasingly studied with the Gene-centered view of evolution by considering inclusive fitness (the carrying on of one's genes through one's family members), rather than merely benefit to the individual.

By cooperating to successfully drive away predators all individuals involved increase their chances of survival and reproduction. An individual stands little chance against a larger predator, but when a large group is involved, the risk to each group member is minimized. By being in a large group, the risk for a particular individual is reduced or diluted. This so-called dilution effect proposed by W. D. Hamilton is another way of explaining the benefits of cooperation by selfish individuals. Lanchester's laws also provide an insight into the advantages of attacking in a large group rather than individually. [13][14]

Another interpretation involves the use of the handicap principle. Here the idea is that a mobbing bird, by apparently putting itself at risk, displays its status and health so as to be preferred by potential partners.[15]

[edit] References

  1. ^ a b Dominey, Wallace J. (1983). "Mobbing in Colonially Nesting Fishes, Especially the Bluegill, Lepomis macrochirus". Copeia 1983 (4): 1086–1088. doi:10.2307/1445113. 
  2. ^ a b c Alcock, John (1998). Animal Behavior: An Evolutionary Approach, 6th edition, Sunderland: Sinauer Associates. ISBN 0-87893-009-4. 
  3. ^ Kruuk, H. (1964). Predators and anti-predator behaviour of the black-headed gull Larus ridibundus, Behaviour Supplements (11). Leiden: E.J. Brill. OCLC 1502972. 
  4. ^ Curio, E. (1978). "The adaptive significance of avian mobbing. I. Teleonomic hypotheses and predictions". Zeitschrift fur Tierpsychologie 48: 175–183. 
  5. ^ Curio, E.; U. Ernst; W. Vieth (1978). "Cultural Transmission of Enemy Recognition: One Function of Mobbing". Science 202: 899–901. 
  6. ^ Tinbergen, Niko [1960] (1989). The herring gull's world: a study of the social behavior of birds. New York: Lyons and Bulford. ISBN 1-55821-049-0. 
  7. ^ Cullen, E. (1957). "Adaptations in the kittiwake to cliff nesting". Ibis 99: 275–302. doi:10.1111/j.1474-919X.1957.tb01950.x. 
  8. ^ Ditte K. Hendrichsen, Peter Christiansen, Elsemarie K. Nielsen, Torben Dabelsteen & Peter Sunde, (2006) "Exposure affects the risk of an owl being mobbed – experimental evidence" Journal of Avian Biology 37(1): 13–18
  9. ^ Coss, Richard G. (1997). "Individual Variation in the Antisnake Behavior of California Ground Squirrels (Spermophilus beecheyi)". Journal of Mammalogy 78 (2): 294–310. 
  10. ^ Brown, C. H. (1982). "Ventriloquial and locatable vocalizations in birds". Zeitschrift fur Tierpsychologies 59: 338–350. 
  11. ^ Leger, Daniel W.; Laura F. Carroll (1981). "Mobbing Calls of the Phainopepla". The Condor 83 (4): 377–380. doi:10.2307/1367509. 
  12. ^ Parker, Geoffrey A., Manfred Milinski (1997). "Cooperation under Predation Risk: A Data-Based ESS Analysis.". Proceedings: Biological Sciences 264 (1385): 1239–1247. doi:10.1098/rspb.1997.0171. 
  13. ^ Kelly, Kevin (1994). Out of control: the new biology of machines, social systems and the economic world. Boston: Addison-Wesley. ISBN 0-201-48340-8. 
  14. ^ Hamilton, W. D. 1971. Geometry for the selfish herd. J. theor. Biol. 31:295-311.
  15. ^ Arnold, K. E. (2000). "Group Mobbing Behaviour and Nest Defence in a Cooperatively Breeding Australian Bird". Ethology 106: 385–393. doi:10.1046/j.1439-0310.2000.00545.x. 

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