Information about Handicap Principle
The handicap principle is a hypothesis originally proposed in 1975 by biologist Amotz Zahavi[1][2][3] to explain how evolution may lead to "honest" or reliable communication between animals who have an obvious motivation to bluff or deceive each other. The handicap principle suggests that reliable signals must be burdensomely costly to the signaller, costing the signaller in the trait being signalled in a manner that an individual with less of that trait could not afford. For example, in the case of sexual selection, the theory suggests that animals of greater quality communicate this status through handicapping behaviour or morphology that effectively lowers their quality. The central idea is that sexually selected traits function like conspicuous consumption, signalling the ability to afford to squander a resource simply by squandering it. Receivers know that the signal indicates quality because inferior quality signallers cannot afford to produce such wastefully extravagant signals.
The generality of the phenomenon is the matter of some debate and disagreement, Zahavi's views on the scope and importance of handicaps in biology remain outside the mainstream.[4] Nevertheless, the idea has been very influential,[5][6][7] with most researchers in the field believing that the theory explains some aspects of animal communication.
Counter-examples to handicap models predate handicap models themselves. Models of signals, such as threat displays, without any handicapping costs show that conventional signalling may be evolutionarily stable in biological communication[23] Further, analysis of some begging models also shows that, in addition to the handicapped outcomes, non-communication strategies are not only evolutionarily stable, but lead to higher payoffs for both players.[24][25]
The handicap principle gains further support by providing interpretations for behaviours that fit into a single unifying gene-centered view of evolution and making earlier explanations based on group selection obsolete. A classic example is that of stotting in gazelles. This behaviour consists in the gazelle initially running slowly and jumping high when threatened by a predator such as a lion or cheetah. The explanation based on group selection was that such behaviour might be adapted to alerting other gazelle to a cheetah's presence or might be part of a collective behaviour pattern of the group of gazelle to confuse the cheetah. Instead, Zahavi proposed that each gazelle was communicating to the cheetah that it was a fitter individual than its fellows and that the predator should avoid chasing it.
The generality of the phenomenon is the matter of some debate and disagreement, Zahavi's views on the scope and importance of handicaps in biology remain outside the mainstream.[4] Nevertheless, the idea has been very influential,[5][6][7] with most researchers in the field believing that the theory explains some aspects of animal communication.
Handicap models
Though the idea was initially controversial[9][10][11][12] (John Maynard Smith being one notable early critic of Zahavi's ideas[13][14][15]) it has gained wider acceptance due to supporting game theoretic models, most notably Alan Grafen's signalling game model.[16] Grafen's model is essentially a rediscovery of Michael Spence's job market signalling model,[17] where the signalled trait was conceived as a courting male's quality, signalled by investment in an extravagant trait -such as the peacock's tail- rather than an employee signalling their quality by way of an expensive education. In both cases, it is the decreased cost to higher quality signallers of producing increased signal that stabilizes the reliability of the signal (Fig. 2). Further formal game theoretical signalling models demonstrated the evolutionary stability of handicapped signals in nestling begging calls[18] predator deterrent signals[19] and threat displays.[20][21] In the classic handicapped models of begging, all players are assumed to pay the same amount to produce a signal of a given level of intensity, but differ in the relative value of eliciting the desired response (donation) from the receiver (Fig. 3).Counter-examples to handicap models predate handicap models themselves. Models of signals, such as threat displays, without any handicapping costs show that conventional signalling may be evolutionarily stable in biological communication[23] Further, analysis of some begging models also shows that, in addition to the handicapped outcomes, non-communication strategies are not only evolutionarily stable, but lead to higher payoffs for both players.[24][25]
Generality and empirical examples
The theory predicts that a sexual ornament, or any other signal, must be costly if it is to accurately advertise a trait of relevance to an individual with conflicting interests. Typical examples of handicapped signals include bird songs, the peacock's tail, courtship dances, bowerbird's bowers, or even possibly jewellery and humor. Jared Diamond has proposed that certain risky human behaviours, such as bungee jumping, may be expressions of instincts that have evolved through the operation of the handicap principle. Zahavi has invoked the potlatch ceremony as a human example of the handicap principle in action. This interpretation of potlatch can be traced to Thorstein Veblen's use of the ceremony in his book Theory of the Leisure Class as an example of "conspicuous consumption".[26]The handicap principle gains further support by providing interpretations for behaviours that fit into a single unifying gene-centered view of evolution and making earlier explanations based on group selection obsolete. A classic example is that of stotting in gazelles. This behaviour consists in the gazelle initially running slowly and jumping high when threatened by a predator such as a lion or cheetah. The explanation based on group selection was that such behaviour might be adapted to alerting other gazelle to a cheetah's presence or might be part of a collective behaviour pattern of the group of gazelle to confuse the cheetah. Instead, Zahavi proposed that each gazelle was communicating to the cheetah that it was a fitter individual than its fellows and that the predator should avoid chasing it.
Immunocompetence handicaps
The theory of immunocompetence handicaps suggests that androgen-mediated traits accurately signal condition due to the immunosuppressive effects of androgens[27]. This immunosuppression may be either because testosterone alters the allocation of limited resources between the development of ornamental traits and other tissues, including the immune system[28], or because heightened immune system activity has a propensity to launch autoimmune attacks against gametes, such that suppression of the immune system enhances fertility[29] Healthy individuals can afford to suppress their immune system by raising their testosterone levels, which also augments secondary sexual traits and displays. A review of empirical studies into the various aspects of this theory found weak support[30].See also
References
1. ^ Zahavi, A. (1975) Mate selection - a selection for a handicap. Journal of Theoretical Biology 53: 205-214.
2. ^ Zahavi, A. (1977) The cost of honesty (Further remarks on the handicap principle). Journal of Theoretical Biology 67: 603-605.
3. ^ Zahavi, A. and Zahavi, A. (1997) The handicap principle: a missing piece of Darwin's puzzle. Oxford University Press. Oxford. ISBN 0-19-510035-2
4. ^ Andrew Pomiankowski, A. & Iwasa, Y. 1998. Handicap Signaling: Loud and True? Evolution, 52, 928-932
5. ^ Johnstone, R.A. (1995) Sexual selection, honest advertisement and the handicap principle: reviewing the evidence" Biological Reviews 70 1-65.
6. ^ Johnstone, R.A. (1997) The evolution of animal signals, In Behavioural Ecology: an evolutionary approach 4th ed., J. R. Krebs and N. B. Davies, editors. Blackwell. Oxford, pp:155-178.
7. ^ Maynard Smith, J. and Harper, D. (2003) Animal Signals. Oxford University Press. ISBN 0-19-852685-7.
8. ^ Johnstone97
9. ^ Davis, J. W. F., & O’Donald, P. (1976). Sexual selection for a handicap: A critical analysis of Zahavi’s model. Journal of Theoretical Biology, 57, 345–354.
10. ^ Eshel, I. (1978). On the handicap principle — a critical defence. Journal of Theoretical Biology, 70, 245–250
11. ^ Kirkpatrick, M (1986) The handicap mechanism of sexual selection does not work. American Naturalist 127:222-240.
12. ^ Pomiankowski, A. (1987). Sexual selection: The handicap principle does work sometimes. Proc. R. Soc. Lond., Series B, 231, 123–145.
13. ^ Maynard Smith, J. (1976). Sexual selection and the handicap principle. Journal of Theoretical Biology, 57, 239–242
14. ^ Maynard Smith, J. (1978). The handicap principle — a comment. Journal of Theoretical Biology,70, 251–252
15. ^ Maynard Smith, J. (1985). Mini review: Sexual selection, handicaps and true fitness. Journal of Theoretical Biology, 115, 1–8.
16. ^ Grafen, A. (1990) Biological signals as handicaps. Journal of Theoretical Biology 144:517-546.
17. ^ Spence, A.M. (1973) Job Market Signaling. Quarterly Journal of Economics 87:355-374.
18. ^ Godfray, H.C.J. 1991. Signalling of need by offspring to their parents, Nature 352 328-330.
19. ^ Yachi, S. 1995. How can honest signalling evolve? The role of the handicap principle. Proceedings of the Royal Society of London, series B 262 283-288.
20. ^ Adams, E.S. & Mesterton-Gibbons, M. 1995. The cost of threat displays and the stability of deceptive communication. Journal of Theoretical Biology 175 405-421.
21. ^ Kim, Y-G. 1995. Status signalling games in animal contests. Journal of Theoretical Biology 176, 221-231.
22. ^ Johnstone97
23. ^ Enquist, M. 1985. Communication during aggressive interactions with particular reference to variation in choice of behaviour. Animal Behaviour 33 1152-1161.
24. ^ Rodriguez-Girones, M.A., Cotton, P.A. & Kacelnik, A. 1996. The evolution of begging: signaling and sibling competition. Proceedings of the National Academy of Sciences USA, 93:14637-14641.
25. ^ Lachmann, M. & Bergstrom, C.T. 1998. Signalling among relatives. II. Beyond the tower of babel. Theoretical Population Biology, 54:146-160.
26. ^ Bliege Bird, R. and Smith, E. A. (2005). Signalling theory, strategic interaction, and symbolic capital. Current Anthropology, 46(2), 221-248.
27. ^ Folstad, I. & Karter, A.K. (1992) Parasites, bright males, and the immunocompetence handicap. American Naturalist 139:603-622.
28. ^ Wedekind, C. and Folstad, I. (1994) Adaptive or non-adaptive immunosuppression by sex hormones? American Naturalist 143:936-38.
29. ^ Folstad, I. & Sakrstein, F. (1996) Is male germ line control creating avenues for female choice? Behavioral Ecology 8:109-112
30. ^ Roberts, M.L., Buchanan K.L., Evans, M.R. (2004). Testing the immunocompetence handicap hypothesis: a review of the evidence. Animal Behaviour. 68:227-239
2. ^ Zahavi, A. (1977) The cost of honesty (Further remarks on the handicap principle). Journal of Theoretical Biology 67: 603-605.
3. ^ Zahavi, A. and Zahavi, A. (1997) The handicap principle: a missing piece of Darwin's puzzle. Oxford University Press. Oxford. ISBN 0-19-510035-2
4. ^ Andrew Pomiankowski, A. & Iwasa, Y. 1998. Handicap Signaling: Loud and True? Evolution, 52, 928-932
5. ^ Johnstone, R.A. (1995) Sexual selection, honest advertisement and the handicap principle: reviewing the evidence" Biological Reviews 70 1-65.
6. ^ Johnstone, R.A. (1997) The evolution of animal signals, In Behavioural Ecology: an evolutionary approach 4th ed., J. R. Krebs and N. B. Davies, editors. Blackwell. Oxford, pp:155-178.
7. ^ Maynard Smith, J. and Harper, D. (2003) Animal Signals. Oxford University Press. ISBN 0-19-852685-7.
8. ^ Johnstone97
9. ^ Davis, J. W. F., & O’Donald, P. (1976). Sexual selection for a handicap: A critical analysis of Zahavi’s model. Journal of Theoretical Biology, 57, 345–354.
10. ^ Eshel, I. (1978). On the handicap principle — a critical defence. Journal of Theoretical Biology, 70, 245–250
11. ^ Kirkpatrick, M (1986) The handicap mechanism of sexual selection does not work. American Naturalist 127:222-240.
12. ^ Pomiankowski, A. (1987). Sexual selection: The handicap principle does work sometimes. Proc. R. Soc. Lond., Series B, 231, 123–145.
13. ^ Maynard Smith, J. (1976). Sexual selection and the handicap principle. Journal of Theoretical Biology, 57, 239–242
14. ^ Maynard Smith, J. (1978). The handicap principle — a comment. Journal of Theoretical Biology,70, 251–252
15. ^ Maynard Smith, J. (1985). Mini review: Sexual selection, handicaps and true fitness. Journal of Theoretical Biology, 115, 1–8.
16. ^ Grafen, A. (1990) Biological signals as handicaps. Journal of Theoretical Biology 144:517-546.
17. ^ Spence, A.M. (1973) Job Market Signaling. Quarterly Journal of Economics 87:355-374.
18. ^ Godfray, H.C.J. 1991. Signalling of need by offspring to their parents, Nature 352 328-330.
19. ^ Yachi, S. 1995. How can honest signalling evolve? The role of the handicap principle. Proceedings of the Royal Society of London, series B 262 283-288.
20. ^ Adams, E.S. & Mesterton-Gibbons, M. 1995. The cost of threat displays and the stability of deceptive communication. Journal of Theoretical Biology 175 405-421.
21. ^ Kim, Y-G. 1995. Status signalling games in animal contests. Journal of Theoretical Biology 176, 221-231.
22. ^ Johnstone97
23. ^ Enquist, M. 1985. Communication during aggressive interactions with particular reference to variation in choice of behaviour. Animal Behaviour 33 1152-1161.
24. ^ Rodriguez-Girones, M.A., Cotton, P.A. & Kacelnik, A. 1996. The evolution of begging: signaling and sibling competition. Proceedings of the National Academy of Sciences USA, 93:14637-14641.
25. ^ Lachmann, M. & Bergstrom, C.T. 1998. Signalling among relatives. II. Beyond the tower of babel. Theoretical Population Biology, 54:146-160.
26. ^ Bliege Bird, R. and Smith, E. A. (2005). Signalling theory, strategic interaction, and symbolic capital. Current Anthropology, 46(2), 221-248.
27. ^ Folstad, I. & Karter, A.K. (1992) Parasites, bright males, and the immunocompetence handicap. American Naturalist 139:603-622.
28. ^ Wedekind, C. and Folstad, I. (1994) Adaptive or non-adaptive immunosuppression by sex hormones? American Naturalist 143:936-38.
29. ^ Folstad, I. & Sakrstein, F. (1996) Is male germ line control creating avenues for female choice? Behavioral Ecology 8:109-112
30. ^ Roberts, M.L., Buchanan K.L., Evans, M.R. (2004). Testing the immunocompetence handicap hypothesis: a review of the evidence. Animal Behaviour. 68:227-239
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A hypothesis (from Greek ὑπόθεσις) consists either of a suggested explanation for a phenomenon or of a reasoned proposal suggesting a possible correlation between multiple phenomena.
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Biology (from Greek: βίος, bio, "life"; and λόγος, logos, "knowledge"), also referred to as the biological sciences, is the scientific study of life.
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Amotz Zahavi (born 1928 in Petach Tikva, Israel) is an Israeli evolutionary biologist from Tel-Aviv University, and one of the founders of the Israeli Society for the Protection of Nature.
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Animal communication is any behaviour on the part of one animal that has an effect on the current or future behaviour of another animal. The study of animal communication, sometimes called zoosemiotics
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Sexual selection is the theory proposed by Charles Darwin that states that the frequency of traits can increase or decrease depending on the attractiveness of the bearer. Biologists today distinguish between "male to male combat" (it is usually males who fight), "mate choice"
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Fitness (often denoted in population genetics models) is a central concept in evolutionary theory. It describes the capability of an individual of certain genotype to reproduce, and usually is equal to the proportion of the individual's genes in all the genes of the next generation.
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Within evolutionary biology, signalling theory refers to a body of theoretical work examining communication between individuals. The central question is when animals with conflicting interests should be expected to communicate "honestly".
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Ethology (from Greek: ήθος, ethos, "custom"; and λόγος, logos, "knowledge") is the scientific study of animal behavior, and a branch of zoology.
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The term morphology in biology refers to the outward appearance (shape, structure, color, pattern) of an organism or taxon and its component parts. This is in contrast to physiology, which deals primarily with function.
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Sexual selection is the theory proposed by Charles Darwin that states that the frequency of traits can increase or decrease depending on the attractiveness of the bearer. Biologists today distinguish between "male to male combat" (it is usually males who fight), "mate choice"
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Conspicuous consumption is a term used to describe the lavish spending on goods and services that are acquired mainly for the purpose of displaying income or wealth. In the mind of a conspicuous consumer, such display serves as a means of attaining or maintaining social status.
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Professor John Maynard Smith,[1] F.R.S. (6 January 1920 – 19 April 2004) was a British evolutionary biologist and geneticist. Originally an aeronautical engineer during the Second World War, he then took a second degree in genetics under the well-known biologist J.
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Game theory is a branch of applied mathematics that is often used in the context of economics. It studies strategic interactions between agents. In strategic games, agents choose strategies which will maximize their return, given the strategies the other agents choose.
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Signaling games are dynamic games with two players, the sender (S) and the receiver (R). The sender has a certain type, t, which is given by nature. The sender observes his own type while the receiver does not know the type of the sender.
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Michael Spence
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Born November 7 1943
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Stanford University homepage photo
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In economics, more precisely in contract theory, signalling is the idea that one party (termed the agent) conveys some meaningful information about itself to another party (the ).
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Pavo
Linnaeus, 1758
Species
Pavo cristatus
Pavo muticus
The term peafowl can refer to the two species of bird in the genus Pavo of the pheasant family, Phasianidae.
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Linnaeus, 1758
Species
Pavo cristatus
Pavo muticus
The term peafowl can refer to the two species of bird in the genus Pavo of the pheasant family, Phasianidae.
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In game theory and behavioural ecology, an evolutionarily stable strategy (or ESS; also evolutionary stable strategy) is a strategy which, if adopted by a population of players, cannot be invaded by any alternative strategy.
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In game theory, cheap talk is pre-play communication which carries no cost. For example, in the Prisoner's Dilemma one might add a round of pre-play communication where each player announces the action they intend to take (or alternatively the action they would like the other to
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Sexual selection is the theory proposed by Charles Darwin that states that the frequency of traits can increase or decrease depending on the attractiveness of the bearer. Biologists today distinguish between "male to male combat" (it is usually males who fight), "mate choice"
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Bird songs are certain vocal sounds that birds make. In non-technical use, these are the bird sounds that are melodious to the human ear. In ornithology, bird 'songs' are often distinguished from shorter sounds, which may be termed 'calls'.
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Pavo
Linnaeus, 1758
Species
Pavo cristatus
Pavo muticus
The term peafowl can refer to the two species of bird in the genus Pavo of the pheasant family, Phasianidae.
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Linnaeus, 1758
Species
Pavo cristatus
Pavo muticus
The term peafowl can refer to the two species of bird in the genus Pavo of the pheasant family, Phasianidae.
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Ptilonorhynchidae
GR Gray, 1841
Genera
Ailuroedus
Amblyornis
Archboldia
Chlamydera
Prionodura
Ptilonorhynchus
Scenopooetes
Sericulus
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GR Gray, 1841
Genera
Ailuroedus
Amblyornis
Archboldia
Chlamydera
Prionodura
Ptilonorhynchus
Scenopooetes
Sericulus
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Jewellery (also spelled jewelry, see spelling differences) is a personal ornament, such as a necklace, ring, or bracelet, made from jewels, precious metals or other substance.
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Humour or humor (see spelling differences) is the ability or quality of people, objects, or situations to evoke feelings of amusement in other people. The term encompasses a form of entertainment or human communication which evokes such feelings, or which makes people laugh
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Jared Diamond
Born: 10 September 1937
Boston
Occupation: Nonfiction writer, Professor of Geography at UCLA
Nationality: American
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Born: 10 September 1937
Boston
Occupation: Nonfiction writer, Professor of Geography at UCLA
Nationality: American
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Bungee jumping (or bungy jumping) is the sport that originated from New Zealand and was created by maverick daredevil A J Hackett, and his original jump from a bridge in Greenhithe, Auckland.
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potlatch is a highly complex event or ceremony among certain Indigenous peoples in North America, including nations on the Pacific Northwest coast of the United States and the Canadian province of British Columbia that has been practiced for thousands of years.
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