Arne Traulsen 2026-11-05
Arne Traulsen studies evolutionary game theory and evolutionary dynamics in finite biological populations. His work uses mathematical models to separate the effects of individual interactions, population structure, and chance in natural selection.[ref]
https://www.evolbio.mpg.de/person/12087. Max Planck Institute for Evolutionary Biology profile; research interests
With Martin A. Nowak, Traulsen constructed a 2006 model of group selection in which only individuals reproduced. Offspring stayed in the parent's group; a group reaching a size limit could split, displacing another group. Cooperation could lower an individual's success against nonhelpers within its group while increasing its group's rate of growth and splitting.[ref]
Evolution of cooperation by multilevel selection by Arne Traulsen and Martin A. Nowak. PNAS 103, pp. 10952–10955; model and Figure 1
The model supplies an illuminating distinction between levels of description. A trait's frequency can fall within mixed groups yet rise in the combined biological population when more cooperative groups contribute more descendants. Specifying the reproduction and splitting rules made this proposal testable by calculation and simulation, rather than inferring an evolutionary advantage solely from a benefit to the group.[ref]
Arne Traulsen
. Photograph by Michael Hesse, identified and credited on the Max Planck institutional profile. Cryptic species Created 2026-10-25 Updated 2026-11-05
Distinct evolutionary lineages or reproductively isolated species that are difficult to distinguish using the morphological characters traditionally examined. Similar appearance can therefore conceal species boundaries. Genetic evidence alone also requires interpretation, because population structure need not imply complete reproductive isolation.
Group selection 2026-11-05
Group selection is a contribution to natural selection arising because groups differ in their survival, growth or production of descendant groups. A heritable trait can spread through greater success of groups containing it even while its frequency declines within each mixed group. For cooperation, the essential question is whether this difference between groups can overcome an individual's cost in biological fitness.
Consider a hypothetical biological population with two groups of 100 individuals: one contains 80 cooperators and the other 20. Initially, the overall cooperative fraction is . Suppose the first group grows to 200 individuals with 75% cooperators, while the second remains at 100 with 15% cooperators. Cooperation has declined within both groups, yet the combined cooperative fraction isThe more cooperative group now contributes more individuals to the total. These invented counts illustrate why within-group change and changes in group weights must both be measured; they do not establish the cause of a real group's growth.
In a 2006 model, Arne Traulsen and Martin A. Nowak made this mechanism explicit: individuals reproduced within groups, groups could split on reaching a size limit, and a split displaced another group. Groups with more cooperators could split more often despite the within-group advantage of withholding help. The population structure and rules governing group persistence therefore mattered alongside individual biological fitness.[ref]
Evolution of cooperation by multilevel selection by Arne Traulsen and Martin A. Nowak. PNAS 103, pp. 10952–10955; abstract, Figure 1 and model definition
Hisashi Ohtsuki 2026-11-05
Hisashi Ohtsuki develops mathematical models of cooperation, connecting population structure with natural selection. His research asks how costly help can persist when individuals that withhold help can still receive its benefits.[ref]
https://rcies.soken.ac.jp/scientists/scientists_hisashi_ohtsuki_en.html. Institutional research profile; mathematical biology and evolution of cooperation
In a 2006 study, Ohtsuki and colleagues represented individuals by graph vertices and their interactions by graph edges. They calculated when a single cooperator had a fixation probability above its neutral benchmark. The result depended on how reproduction filled vacant sites, as well as on the graph. This helped make network reciprocity a quantitative mechanism: local interaction patterns and the updating rule can alter whether helping is favoured. The analysis used weak selection and large-population approximations, so the resulting threshold must be read with those assumptions.[ref]
A simple rule for the evolution of cooperation on graphs and social networks by Hisashi Ohtsuki and others. Nature 441, pp. 502–504; model, fixation criterion and update-rule comparison
Hisashi Ohtsuki
. Portrait identified on the SOKENDAI institutional profile. Inclusive fitness Created 2026-10-20 Updated 2026-11-05
A framework combining an actor’s effects on its own reproduction with effects on others, weighted by appropriate genetic relatedness and reproductive values. Coefficients and marginal effects depend on the model and population structure.
Outcrossing Created 2026-10-20 Updated 2026-11-05
Mating between different individuals; its consequences depend on population structure and the compatibility of their alleles.
