Biological Markets

a summary

Yellow baboon males in Amboseli National Park, Kenya

photo R. Noë

Partner choice is an essential ingredient of biological markets

For my comments on any new Biological Market papers, please follow this link:

Biological Markets on ScoopIt!

A video-taped talk on Biological Markets (IIASA, Austria, 2009)

More information about BMs on the pages of the workshop "Cooperation in multi-partner settings"

(Lorentz Center, Leiden, The Netherlands 16-20 JAN 2012)


If you think your paper(s) should be listed on this site, then feel free to contact me: ronald.noe [at] gmail.com

(I am preparing a book on biological markets and only add few new references to this site)

The label 'biological markets' was proposed by Noë & Hammerstein (1994; 1995) for all interactions between organisms in which one can recognise different classes of 'traders' that exchange commodities, such as goods (e.g. food, shelter, gametes) or services (e.g. warning calls, protection, pollination).

 

The characteristics of biological markets are found in mating systems ('mating markets'), mutualisms between members of different species and cooperation among conspecifics

 

The term 'market' was chosen because it is assumed that shifts in supply and demand cause changes in the exchange value of the commodities traded. Important phenomena are: partner choice and outbidding.

 

Formal properties of Biological Markets 

  • Commodities are exchanged between individuals that differ in the degree of control over these commodities
  • Trading partners are chosen from a number of potential partners.
  • There is competition among the members of the chosen class to be the most attractive partner. This competition by 'outbidding' causes an increase in the value of the commodity offered.
  • Supply and demand determine the bartering value of commodities exchanged.
  • Commodities on offer can be advertised. As in commercial advertisements there is a potential for false information.

 

Explicitly excluded is the use of physical force or threat to appropriate commodities or to eliminate the competition. The use of force is common, of course, as are theft and foul play in human markets, but one needs different paradigms to describe these phenomena.

 

For reviews on Biological Market Theory applied to humans see: Barclay, P. 2013. Strategies for cooperation in biological markets, especially for humans. Evolution and Human Behavior 34,164-175 and Barclay, P. (2015). Biological markets and the effects of partner choice on cooperation and friendship. Current Opinion in Psychology


 

Biological Market Theory (BMT) and Reciprocal Altruism (RA)

Biological Market theory (BMT) is not, as some seem to think, an 'extension' of Trivers' reciprocal altruism (RA) paradigm. However, RA and other ‘partner control models’ can describe cooperative relationships reasonably well when the costs of partner choice and partner switching are high. Two of the examples Trivers used in his 1971 classic on RA, coalition formation among male baboons and cleaner fish mutualisms, are explained more accurately by BMT. A recent review of the literature on food sharing in vampire bats, another example Trivers used, suggests that this might be better described as a market too (Carter & Wilkinson, 2013. Does food sharing in vampire bats demonstrate reciprocity? Communicative & Integrative Biology, 6, e25783) pdf. Gerald Carter advocates the use of the term 'reciprocity' in a broad sense, however, and sees partner control and partner choice models as part of a continuum (The reciprocity controversy). See also Gerald Carter's website & blog: http://socialbat.org/


A common fallacy: reciprocity and time frames

In the primate literature ‘reciprocity’ is often confused with Trivers’ ‘reciprocal altruism’ (RA). Reciprocity, however, is an observed phenomenon: two animals exchanging altruistic acts do that more or less equally often. RA is a so-called ‘partner control’ mechanism that can result in reciprocity. Indeed, the lack of reciprocity disproves RA. However, the opposite is not true as reciprocity can result from other mechanisms, such as the ‘partner choice’ mechanisms advocated by biological market theory (BMT). Reciprocity is often found to be more pronounced when measured over longer time frames. This is not surprising; variable things tend to equal out as time passes. A recent paper by Campennì & Schino confirms this (Campennì, M., & Schino, G. (2014). Partner choice promotes cooperation: The two faces of testing with agent-based models. Journal of Theoretical Biology, 344, 49-55 pdf)

To prove RA, however, one should look at extremely short time frames, say one to three interactions in a row between the same individuals. Crucial is the contingency in the behaviour shown in those interactions. RA is usually modelled using repeated games such as the 2-player Iterated Prisoner’s Dilemma to make this point obvious. Partner choice can be based on interactions over much longer time frames. If ‘attitudinal partner choice’ (Fruteau et al 2009) plays the role I think it plays, then certain partners are preferred on the basis of their long term reliability or willingness to help. BMT can explain why such partnerships can be lop-sided over both shorter and longer time frames. It is a mistake to think that BMT predicts fast fluctuations only. It predicts adaptations to supply and demand, but it depends on the mechanism involved how fast these adaptations are. It also depends on the commodities involved whether partner values are likely to change over short or long periods. For example: a high-ranking monkey will remain a valuable partner when it comes to giving support in conflicts over long periods of time, but a monkey mother of a young infant may loose value quickly as a partner when new infants are born and her own infant grows older.