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Social selection is a hypothesis proposed by Joan Roughgarden as an alternative to sexual selection. Social selection is argued to be a mode of natural selection based on reproductive transactions and a two-tiered approach to evolution and the development of social behavior.[1] Reproductive transactions refer to a situation where one organism offers assistance to another in exchange for access to reproductive opportunity. The two tiers of the theory are behavioral and population genetic.[1][2] The genetic aspect states that anisogamy arose to maximize contact rate between gametes. The behavioral aspect is concerned with cooperative game theory and the formation of social groups to maximize the production of offspring.

In her critique against the neo-Darwinian defense of sexual selection, Roughgarden outlines exceptions to many of the assumptions that come with sexual selection.[1] These exceptions include sexually monomorphic species, species which reverse standard sex roles, species with template multiplicity, species with transgender presentation, frequencies of homosexual mating, and the lack of correlation between sexually selected traits and deleterious mutation.[3] An article published by Roughgarden's lab on her ideas received criticism in the journal Science. Forty scientists produced ten critical letters. The critics stated that the article was misleading, that it contained misunderstandings and misrepresentations, that sexual selection accounted for all the data presented and subsumed Roughgarden's theoretical analysis, and that sexual selection explained data that her theory could not.[4][5]

Other researchers, such as biologist Mary Jane West-Eberhard and evolutionary medicine researcher Randolph M. Nesse, instead view sexual selection as a subcategory of social selection,[list 1] with Nesse and anthropologist Christopher Boehm arguing further that altruism in humans held fitness advantages that enabled evolutionarily extraordinary cooperativeness and the human capability of creating culture, as well as capital punishment by band societies against bullies, thieves, free-riders, and psychopaths.[list 2]

Genetic principles

Portfolio hypothesis

Short for the genetic-portfolio balancing hypothesis, this idea, proposed by Roughgarden, is used as an alternative to the Red Queen and Mueller's ratchet hypotheses to explain the existence of sexual reproduction within the framework of social selection.[1] In a population with two species which fit the same ecological niche, live in the same local environment, have the same degree of genetic diversity, but have different modes of reproduction, sexual and asexual, the sexual species will eventually dominate the local environment. This is due to asexual populations losing diversity for short-term adaptations to the environment.

Roughgarden proposes a population of dandelions which fit the above description. The parental generation of a sexually reproducing species and asexually reproducing species contains equal ratios of the three genotypes (A1A1, A1A2, and A2A2). The F1 generation of the asexual dandelions will contain the same ratio as the P-generation. Conversely, following standard principles of sexual reproduction, the F1 generation will be 25% A1A1, 25% A2A2, and 50% A1A2. With the addition of differential survival related to these genotypes (certain genotypes surviving better in different degrees of sunlight), the asexual population will eventually drift toward one genotype and die off when the environment changes to suit a different genotype. The sexual population in the same situation will remain diverse enough to survive changing environments.

From this theory, Roughgarden concludes that the main benefit of sexual reproduction is the maintenance of genetic diversity when compared to similar asexual populations.

The IR model of the development of anisogamy

The IR model for the development of anisogamy is named after its developers Priya Iyer and Joan Roughgarden. By considering the evolution of anisogamy in hermaphroditic marine invertebrates and bisexual plants, the theory postulates of a gene locus which controls both sperm and egg size produced by an organism. Anisogamy could evolve in diploid hermaphroditic adults as an individual adaptation which increases its own fitness.[18]

Hermaphrodism

Hermaphroditic animals and dioecious plants represent a large portion of sexually reproductive species. Under social selection theory, species where individuals produce two different gametes predate strictly gonochoristic and monoecious species. Separate sexes can, therefore, be described as derivations of primal hermaphrodites.[1]

Males arising in primarily hermaphroditic species gain an advantage in certain environments as fertilizers because they lack the energy cost of producing eggs.[19] The development of monoecious and gonochoristic species represents a transition from broadcast fertilization to localized and internal fertilization.[1]

The Broad-barred goby is capable of bi-directional sex change.
The Broad-barred goby is capable of bi-directional sex change.

Simultaneous hermaphrodism exists in species with pre-Cambrian roots, and several families of organisms have shifted between hermaprodism and gonochoism over their evolutionary history.[1] There are sequentially hermaphroditic species, such as the goby, which show bidirectional sex changing. The dwarf males of anglerfish in the family Ceratiidae function as "mobile testes" for the females of their species.

Behavioral principles

Reproductive transactions

Animals help another in order to access reproductive opportunities. Any inequality in this opportunity is due to predation or resource availability. Therefore, there is value in boosting the reproductive fitness of an animals parents or siblings, both of which share genetic information. Even without this genetic relationship, reproductive transactions can be valuable. Sexual conflict arises from a failure for pairs to negotiate value of reproductive transactions effectively.[1]

Mating can therefore serve purposes beyond reproduction, if the maintenance of social structures does not decrease effective fitness. Homosexual mating behavior is observed in species where this is the case. Several asexual species of whiptail lizards have been observed to engage in mating and pair-bonding despite the lack of gametic fusion.[20]

Social state matrices

Animal behavior can be understood as the intersection of three primary elements: genetic foundations, social systems, and individual reaction. A social state matrix is composed of genetic foundations and social systems to determine behavior arising from the intersection of them.[1] For example, animals have genetics which determine reaction to potential foraging stimuli, but only search for the stimuli at certain times of day due to social systems. Therefore, social systems would be selected for which optimize behaviors such as foraging and mate selection.

Criticism

Presented as an alternative to sexual selection theory, social selection has received criticism as a result. Arguments have been made that Roughgarden anthropomorphizes animal behavior in order to suit her theory.[21] Other critics argue that the holes in sexual selection theory which Roughgarden proposes, such as inconsistencies in male and female relationships and critiques of Bateman's principle, can actually be consolidated within the sexual selection framework.[22]

An article published by Roughgarden's lab on these ideas received criticism in the journal Science. Forty scientists produced ten critical letters. The critics stated that the article was misleading, that it contained misunderstandings and misrepresentations, that sexual selection accounted for all the data presented and subsumed Roughgarden's theoretical analysis, and that sexual selection explained data that her theory could not.[4][5] Roughgarden stated she was "not altogether surprised" by the volume of dissent and that her theory was not an extension of sexual selection theory.[4][5]

Alternate uses of the term

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The term "social selection" has been used by other researchers to describe elements of the selection process overlooked by the theory of sexual selection, and to view sexual selection as a subcategory of social selection.[6][7][11] Mary Jane West-Eberhard used the term social selection to describe differential success in social competition for resources other than mates,[8] which includes female competition for territory and competition for parental attention among offspring.[9] Citing cross-cultural research conducted by social psychologist David Buss,[23][24] psychologist Geoffrey Miller has argued that if humans prefer altruistic mating partners that would select by mate choice for altruism directly,[25] while evolutionary medicine researcher Randolph M. Nesse has argued that humans with altruistic tendencies receive fitness advantages because they are preferred as social partners,[14] and this enabled humans as a species of becoming extraordinarily cooperative and capable of creating culture.[15]

References

  1. ^ a b c d e f g h i Roughgarden, Joan (2009). Genial Gene. California: The Regents of University of California. ISBN 978-0-520-25826-6.
  2. ^ Roughgarden, Joan; Açkay, Erol. "Do we need a Sexual Selection 2.0?". The Association for the Study of Animal Behaviour.
  3. ^ Roughgarden, Joan; Akçay, Erol (2009). "Final response:sexual selection needs an alternative". The Association for the Study of Animal Behaviour.
  4. ^ a b c Atkinson, Nick (May 5, 2006). "Sexual selection alternative slammed". The Scientist. Archived from the original on 2007-09-29. Retrieved 2007-05-15.
  5. ^ a b c Dall, S. R. X.; McNamara, J. M.; Wedell, N.; Hosken, D. J. (2006-05-05). "Debating Sexual Selection and Mating Strategies" (PDF). Science. 312 (5774): 689b–697b. doi:10.1126/science.312.5774.689b. PMID 16675684. S2CID 10887773. Retrieved 14 June 2021.
  6. ^ a b West-Eberhard, Mary Jane (1975). "The Evolution of Social Behavior by Kin Selection". The Quarterly Review of Biology. University of Chicago Press. 50 (1): 1–33. doi:10.1086/408298. JSTOR 2821184. S2CID 14459515.
  7. ^ a b West-Eberhard, Mary Jane (1979). "Sexual Selection, Social Competition, and Evolution". Proceedings of the American Philosophical Society. American Philosophical Society. 123 (4): 222–34. JSTOR 986582.
  8. ^ a b West-Eberhard, Mary Jane (1983). "Sexual Selection, Social Competition, and Speciation". Quarterly Review of Biology. University of Chicago Press. 58 (2): 155–183. doi:10.1086/413215. JSTOR 2828804. S2CID 54711556.
  9. ^ a b West-Eberhard, Mary Jane (2014). "Darwin's forgotten idea: the social essence of sexual selection". Neuroscience & Biobehavioral Reviews. Elsevier. 46 (4): 501–508. doi:10.1016/j.neubiorev.2014.06.015. PMID 25003806. S2CID 1604935.
  10. ^ Lyon, Bruce E.; Montgomerie, Robert (2012). "Sexual selection is a form of social selection". Philosophical Transactions of the Royal Society B. London, UK: Royal Society. 367 (1600): 2266–2273. doi:10.1098/rstb.2012.0012. PMC 3391428. PMID 22777015.
  11. ^ a b Nesse, Randolph (2019). Good Reasons for Bad Feelings: Insights from the Frontier of Evolutionary Psychiatry. Dutton. pp. 172–176. ISBN 978-1101985663.
  12. ^ Boehm, Christopher (1999). "The Natural Selection of Altruistic Traits" (PDF). Human Nature. Springer Science+Business Media. 10 (3): 205–252. doi:10.1007/s12110-999-1003-z. PMID 26196335. S2CID 207392341. Retrieved July 7, 2021.
  13. ^ Boehm, Christopher (2001) [1999]. Hierarchy in the Forest: The Evolution of Egalitarian Behavior (Revised ed.). Cambridge, MA: Harvard University Press. ISBN 978-0674006911.
  14. ^ a b Nesse, Randolph M. (2007). "Runaway social selection for displays of partner value and altruism". Biological Theory. Springer Science+Business Media. 2 (2): 143–55. doi:10.1162/biot.2007.2.2.143. S2CID 195097363.
  15. ^ a b Nesse, Randolph M. (2009). "10. Social Selection and the Origins of Culture". In Schaller, Mark; Heine, Steven J.; Norenzayan, Ara; Yamagishi, Toshio; Kameda, Tatsuya (eds.). Evolution, Culture, and the Human Mind. Philadelphia: Taylor & Francis. pp. 137–50. ISBN 978-0805859119.
  16. ^ Boehm, Christopher (2012). Moral Origins: Social Selection and the Evolution of Virtue, Altruism, and Shame. New York: Basic Books. ISBN 978-0465020485.
  17. ^ Boehm, Christopher (2014). "The moral consequences of social selection". Behaviour. Brill Publishers. 151 (2–3): 167–183. doi:10.1163/1568539X-00003143. Retrieved July 7, 2021.
  18. ^ Iyer, Priya; Roughgarden, Joan (2008). "Gametic Conflict Versus Contact in the Evolution of Anisogamy". Theoretical Population Biology. 73 (4): 461–72. doi:10.1016/j.tpb.2008.02.002. PMID 18485981.
  19. ^ Iyer, Priya; Roughgarden, Joan (2008). "Dioecy as a Specialization Promoting Sperm Delivery". Evolutionary Ecology Research. 10.
  20. ^ Roughgarden, Joan (2009). Evolution's Rainbow. University of California Press. pp. 129–131. ISBN 978-0520260122.
  21. ^ Milam, Erika L.; Millstein, Roberta L.; Potochnik, Angela; Roughgarden, Joan E. (23 November 2010). "Sex and sensibility: The role of social selection". Metascience. 20 (2): 253–277. doi:10.1007/s11016-010-9464-6. S2CID 17700476.
  22. ^ Clutton-Brock, Tim (2009). "We do not need a Sexual Selection 2.0-nor a theory of Genial Selection". The Association for the Study of Animal Behavior – via Elsevier.
  23. ^ Buss, David M. (1989). "Sex differences in human mate preferences: Evolutionary hypotheses tested in 37 cultures". Behavioral and Brain Sciences. Cambridge University Press. 12 (1): 1–49. doi:10.1017/S0140525X00023992.
  24. ^ Buss, David M. (1995) [1992]. "5. Mate Preference Mechanisms: Consequences for Partner Choice and Intrasexual Competition". In Barkow, Jerome H.; Cosmides, Leda; Tooby, John (eds.). The Adapted Mind: Evolutionary Psychology and the Generation of Culture. New York: Oxford University Press. pp. 253–256. ISBN 978-0195101072.
  25. ^ Miller, Geoffrey F. (2000). The Mating Mind: How Sexual Choice Shaped the Evolution of Human Nature (1st ed.). New York: Doubleday. pp. 292–340. ISBN 978-0385495165.
Bundled references