Abstract
How humans make decisions in noncooperative strategic interactions is a big question. For the fundamental RockPaperScissors (RPS) model game system, classic Nash equilibrium (NE) theory predicts that players randomize completely their action choices to avoid being exploited, while evolutionary game theory of bounded rationality in general predicts persistent cyclic motions, especially in finite populations. However as empirical studies have been relatively sparse, it is still a controversial issue as to which theoretical framework is more appropriate to describe decisionmaking of human subjects. Here we observe populationlevel persistent cyclic motions in a laboratory experiment of the discretetime iterated RPS game under the traditional random pairwisematching protocol. This collective behavior contradicts with the NE theory but is quantitatively explained, without any adjustable parameter, by a microscopic model of winlosetie conditional response. Theoretical calculations suggest that if all players adopt the same optimized conditional response strategy, their accumulated payoff will be much higher than the reference value of the NE mixed strategy. Our work demonstrates the feasibility of understanding human competition behaviors from the angle of nonequilibrium statistical physics.
Introduction
The RockPaperScissors (RPS) game is a fundamental noncooperative game. It has been widely used to study competition phenomena in society and biology, such as species diversity of ecosystems^{1,2,3,4,5,6} and price dispersion of markets^{7,8}. This game has three candidate actions R (rock), P (paper) and S (scissors). In the simplest settings the payoff matrix is characterized by a single parameter, the payoff a of the winning action (a > 1, see Fig. 1A)^{9}. There are the following nontransitive dominance relations among the actions: R wins over S, P wins over R, yet S wins over P (Fig. 1B), so no action is absolutely better than the others.
The RPS game is also a basic model system for studying decisionmaking of human subjects in competitive environments and the associated social dynamics and nonequilibrium physics. Assuming ideal rationality for players who repeatedly playing the RPS game within a population, classical game theory predicts that individual players will completely randomize their action choices so that their behaviors will be unpredictable and not be exploited by the other players^{10,11}. This is referred to as the mixedstrategy Nash equilibrium (NE), in which every player chooses the three actions with equal probability 1/3 at each game round (see Supplementary Notes online). When the payoff parameter a < 2 this NE is evolutionarily unstable with respect to small perturbations but it becomes evolutionarily stable at a > 2 (see Supplementary Notes online)^{12}. On the other hand, evolutionary game theory drops the infinite rationality assumption and looks at the RPS game from the angle of evolution and adaption^{13,14,15,16,17,18}. Evolutionary models based on various microscopic learning rules (such as the replicator dynamics^{12,19,20,21}, the best response dynamics^{22,23} and the logit dynamics^{24,25}) generally predict cyclic evolution patterns for the action marginal distribution (mixed strategy) of each player, especially in finite populations.
Empirical verification of nonequilibrial persistent cycling in the humansubject RPS game (and other noncooperative games) has been rather nontrivial, as the recorded evolutionary trajectories are usually highly stochastic and not long enough to draw convincing conclusions. Two of the present authors partially overcame these difficulties by using social state velocity vectors^{26} and forward and backward transition vectors^{27} to visualize violation of detailed balance in game evolution trajectories, but a simple way of quantitatively measuring persistent cyclic behavoiors in a highly stochastic trajectory was still lacking. The cycling frequency of directional flows in the neutral RPS game (a = 2) was later quantitatively measured in^{28} using a coarsegrained counting technique. Cason and coworkers^{29} using another cycle rotation index as the order parameter also obtained evidence of persistent cycling in some evolutionarily stable RPSlike games, if players were allowed to update actions asynchronously in continuous time and were informed about the social states of the whole population by some sophisticated ‘heat maps’.
In this work we investigate whether cycling is a general aspect even for the simplest RPS game. We adopt an improved cycle counting method on the basis of our earlier experiences^{28} and study directional flows in evolutionarily stable (a > 2) and unstable (a < 2) discretetime RPS games. We show strong evidence that the RPS game is an intrinsic nonequilibrium system, which cannot be fully described by the NE concept even in the evolutionarily stable region but rather exhibits persistent populationlevel cyclic motions. We then bridge the collective cycling behavior and the highly stochastic decisionmaking of individuals through a simple conditional response (CR) mechanism. Our empirical data confirm the plausibility of this microscopic model of bounded rationality. Our theoretical calculations also demonstrate that, if all the players adopt the same CR strategy and if the transition parameters of this strategy are chosen in an optimized way, this CR strategy will outperform the NE mixed strategy in terms of the accumulated payoffs of individual players, yet the action marginal distribution of individual players is indistinguishable from that of the NE mixed strategy. Our work as a successful attempt of understanding competition dynamics from the perspective of nonequilibrium statistical physics may stimulate future more refined experimental and theoretical studies on the microscopic mechanisms of decisionmaking and learning in basic game systems^{19,30,31,32,33,34}.
Results
Experimental system
We recruited a total number of 360 students from different disciplines of Zhejiang University to form 60 disjoint populations of size N = 6. Each population then carries out one experimental session by playing the RPS game 300 rounds (taking 90–150 minutes) with a fixed value of a. In realworld situations individuals often have to make decisions based only on partial input information. We mimic such situations by adopting the traditional random pairwisematching experimental protocol^{11}: At each game round (time) t the players are randomly paired within the population and compete with their pair opponent once; after that each player gets feedback information about her own payoff as well as her and her opponent's action. As the experimental session finishes, the players are paid in real cash proportional to their accumulated payoffs (see Methods). Our experimental setting differs from those of two other recent experiments, in which every player competes against the whole population^{9,29} and may change actions in continuous time^{29}. We set a = 1.1, 2, 4, 9 and 100, respectively, in onefifth of the populations so as to compare the dynamical behaviors in the evolutionarily unstable, neutral, stable and deeply stable regions.
Action marginal distribution of individual players
We observe that the individual players shift their actions frequently in all the populations except one with a = 1.1 (this exceptional population is discarded from further analysis, see Supplementary Notes online). Averaged among the 354 players of these 59 populations, the probabilities that a player adopts action R, P, S at one game round are, respectively, 0.36 ± 0.08, 0.33 ± 0.07 and 0.32 ± 0.06 (mean ± s.d.). We obtain very similar results for each set of populations of the same a value (see Supplementary Table S1 online). These results are consistent with NE and suggest the NE mixed strategy is a good description of a player's marginal distribution of actions. However, a player's actions at two consecutive times are not independent but correlated. As demonstrated in Fig. 2A–2E, at each time the players are more likely to repeat their last action than to shift action either counterclockwise (i.e., R → P, P → S, S → R, see Fig. 1B) or clockwise (R → S, S → P, P → R). This inertial effect is especially strong at a = 1.1 and it diminishes as a increases.
We notice that at a ≥ 2, an individual player's probability of making a clockwise action shift is equal to or just slightly different from that of making a counterclockwise action shift (Fig. 2A–2E). There is no or only very weak cycling behavior at the level of individual players in the evolutionarily neutral (a = 2) and stable (a > 2) RPS games, in accordance with the NE theory. As shown in Fig. 2F–2J, the action shift statistics of individual players can be well explained by the later introduced conditional response model.
Collective behaviors of the whole population
The social state of the population at any time t is denoted as s(t) ≡ (n_{R}(t), n_{P}(t), n_{S}(t)) with n_{q} being the number of players adopting action q ∈ {R, P, S}. Since n_{R} + n_{P} + n_{S} ≡ N there are (N + 1)(N + 2)/2 such social states, all lying on a threedimensional plane bounded by an equilateral triangle (Fig. 1C). Each population leaves a trajectory on this plane as the RPS game proceeds. To detect rotational flows, we assign for every social state transition s(t) → s(t + 1) a rotation angle θ(t), which measures the angle this transition rotates with respect to the centroid c_{0} ≡ (N/3, N/3, N/3) of the social state plane (see Methods)^{28}. Positive and negative θ values signify counterclockwise and clockwise rotations, respectively, while θ = 0 means the transition is not a rotation around c_{0}. For example, we have θ(1) = π/3, θ(2) = 0 and θ(3) = −2π/3 for the three transitions shown in Fig. 1C.
The net number of cycles around c_{0} during the time interval [t_{0}, t_{1}] is computed by
As shown in Fig. 3A–3E, C_{1,t} has an increasing trend in most of the 59 populations, indicating persistent counterclockwise cycling. The cycling frequency of each trajectory in [t_{0}, t_{1}] is evaluated by
The values of f_{1,300} for all the 59 populations are listed in Table 1, from which we obtain the mean frequency to be 0.031 ± 0.006 (a = 1.1, mean ± SEM), 0.027 ± 0.008 (a = 2), 0.031 ± 0.008 (a = 4), 0.022 ± 0.008 (a = 9) and 0.018 ± 0.007 (a = 100). These mean frequencies are all positive irrespective to the particular value of a, indicating that behind the seemingly highly irregular social state evolution process, there is a deterministic pattern of social state cycling from slightly rich in action R, to slightly rich in P, then to slightly rich in S and then back to slightly rich in R again. Statistical analysis confirms that f_{1,300} > 0 is significant for all the five sets of populations (Wilcoxon signedrank test, p < 0.05). The correlation between the mean cycling frequency f_{1,300} and the payoff parameter a is not statistically significant (Spearman's correlation test: r = −0.82, p = 0.19, for n = 5 mean frequencies; and r = −0.16, p = 0.24, for n = 59 frequencies). We also notice that the mean cycling frequency in the second half of the game (f_{151,300}) is slightly higher than that in the first half (f_{1,150}) for all the five sets of populations (Supplementary Table S2 online), suggesting that cycling does not die out with time.
A recent experimental work^{35} also observed cycling behaviors in a RPSlike game with more than three actions. Evidences of persistent cycling in some completeinformation and continuoustime RPSlike games were reported in another experimental study^{29}. However, no (or only very weak) evidence of populationlevel cycling was detected in^{29} if action updating was performed in discrete time. Here and in Ref. 28 we find that even discretetime updating of actions will lead to collective cyclic motions in the RPS game and such a populationlevel behavior is not affected by the particular value of a.
Empirical conditional response patterns
Under the assumption of mixedstrategy NE (i.e., each player chooses the three actions with equal probability at every game round, independent of each other and of the payoffs of previous plays), the social state transitions should obey the detailed balance condition. Therefore the observed persistent cycling behavior cannot be understood within the NE framework. Persistent cycling can also not be explained by the independent decision model which assumes the action choice of a player at one time is influenced only by her action at the previous time (see Supplementary Notes online). Using the empirically determined action shift probabilities of Fig. 2A–2E as inputs, we find that this independent decision model predicts the cycling frequency to be 0.0050 (for a = 1.1), −0.0005 (a = 2), −0.0024 (a = 4), −0.0075 (a = 9) and −0.0081 (a = 100), which are all very close to zero and significantly different from the empirical values.
The action choices of different players must be mutually influenced. Our empirical data shown in Fig. 3F–3J confirm the existence of such mutual influences. Let us denote by O the performance (output) of a player at a given game round, with O ∈ {W (win), T (tie), L (lose)}. Conditional on the output O, the probability that this player will decide to shift action clockwise or counterclockwise or keep the same action in the next play is denoted as O_{−}, O_{+} and O_{0} (≡ 1 − O_{−} − O_{+}), respectively. Most interestingly, we see from Fig. 3F–3J that if a player wins over her opponent in one play, her probability (W_{0}) of repeating the same action in the next play is considerably higher than her probabilities (W_{−} and W_{+}) of shifting actions. Furthermore, for payoff parameter a ≥ 2, if a player loses to her opponent in one play, she is more likely to shift action clockwise (probability L_{−}) than either to keep the old action (L_{0}) or to shift action counterclockwise (L_{+}).
The conditional response model
Inspired by these empirical observations, we develop a simplest nontrival model by assuming the following conditional response strategy: at each game round, every player review her previous performance O ∈ {W, T, L} and makes an action choice according to the corresponding three conditional probabilities (O_{−}, O_{0}, O_{+}). This model is characterized by a set Γ ≡ {W_{−}, W_{+}; T_{−}, T_{+}; L_{−}, L_{+}} of six CR parameters. Notice this CR model differs qualitatively from the discretetime logit dynamics model^{24,25} used in Ref. 28, which assumes each player has global information about the population's social state.
We can solve this winlosetie CR model analytically and numerically (see Supplementary Notes online). Let us denote by n_{rr}, n_{pp}, n_{ss}, n_{rp}, n_{ps} and n_{sr}, respectively, as the number of pairs in which the competition being R–R, P–P, S–S, R–P, P–S and S–R, in one game round t. Given the social state s = (n_{R}, n_{P}, n_{S}) at time t, the conditional joint probability distribution of these six integers is expressed as
where (N − 1)!! ≡ 1 × 3 × … × (N − 3) × (N − 1) and is the Kronecker symbol ( if m = n and = 0 if otherwise). With the help of this expression, we can then obtain an explicit formula for the social state transition probability M_{cr}[s′s] from s to any another social state s′ (see Methods). We then compute numerically the steadystate social state distribution of this Markov matrix^{36} and other average quantities of interest. For example, the mean steadystate cycling frequency f_{cr} of this model is computed by
where θ_{s}_{→s′} is the rotation angle associated with the social state transition s → s′, see Eq. (7).
Using the empirically determined response parameters as inputs, the CR model predicts the mean cycling frequencies for the five sets of populations to be f_{cr} = 0.035 (a = 1.1), 0.026 (a = 2), 0.030 (a = 4), 0.018 (a = 9) and 0.017 (a = 100), agreeing well with the empirical measurements. Such good agreements between model and experiment are achieved also for the 59 individual populations (Fig. 3K–3O). In addition, we find the empirically observed inertial effect of Fig. 2A–2E is quantitatively reproduced by the CR model without any fitting parameter (see Fig. 2F–2J).
Because of the rotational symmetry of the conditional response parameters, the CR model predicts that each player's action marginal distribution is uniform, identical to the NE mixed strategy (Supplementary Notes online). On the other hand, according to this model, the expected payoff g_{cr} per game round of each player is
where g_{0} ≡ (1 + a)/3 is the expected payoff of the NE mixed strategy and τ_{cr} is the average fraction of ties among the N/2 pairs at each game round, with the expression
The value of g_{cr} depends on the CR parameters. By uniformly sampling 2.4 × 10^{9} instances of Γ from the threedimensional probability simplex, we find that for a > 2, g_{cr} has high chance of being lower than g_{0} (Fig. 4), with the mean value of (g_{cr}−g_{0}) being −0.0085(a−2). (Qualitatively the same conclusion is obtained for larger N values, e.g., see Supplementary Fig. S1 online for N = 12.) This is consistent with the mixedstrategy NE being evolutionarily stable^{12}. On the other hand, the four g_{cr} values (for the four cases of a ≠ 2) determined by the empirical CR parameters and the corresponding four mean payoffs of the empirical data sets all weakly exceed g_{0}, indicating that individual players are adjusting their responses to achieve higher accumulated payoffs (Supplementary Notes online). The positive gap between g_{cr} and g_{0} may further enlarge if the individual players were given more learning time to optimize their response parameters (e.g., through increasing the repeats of the game).
As shown in Fig. 4 and Supplementary Fig. S1 online, the CR parameters have to be highly optimized to achieve a large value of g_{cr}. For population size N = 6 we give three examples of the sampled best CR strategies for a > 2: Γ_{1} = {0.002, 0.000; 0.067, 0.110; 0.003, 0.003}, with cycling frequency f_{cr} = 0.003 and g_{cr} = g_{0} + 0.035(a − 2); Γ_{2} = {0.995, 0.001; 0.800, 0.058; 0.988, 0.012}, with f_{cr} = −0.190 and g_{cr} = g_{0} + 0.034(a − 2); Γ_{3} = {0.001, 0.004; 0.063, 0.791; 0.989, 0.001}, with f_{cr} = 0.189 and g_{cr} = g_{0} + 0.033(a − 2). For large a these CR strategies outperform the NE mixed strategy in payoff by about 10%. Set Γ_{1} indicates that populationlevel cycling is not a necessary condition for achieving high payoff values. On the other hand, set Γ_{3} implies W_{0} ≈ 1, L_{0} ≈ 0, therefore this CR strategy can be regarded as an extension of the winstay loseshift (also called Pavlov) strategy, which has been shown by computer simulations to facilitate cooperation in the prisoner's dilemma game^{37,38,39,40}. We should also emphasize that the empirically observed CR transition parameters (Fig. 3F–3J) still differ considerably from those of the winstay loseshift strategy Γ_{3}.
Discussion
In gametheory literature it is common to equate individual players' action marginal distributions with their actual strategies^{11,18}. In reality, however, decisionmaking and learning are very complicated neural processes^{41,42,43,44,45}. The action marginal distributions are only a consequence of such complex dynamical processes, their coarsegrained nature makes them unsuitable to describe dynamical properties^{17}. Our work on the finitepopulation RPS game clearly demonstrates this point. This game exhibits persistent cyclic motions at the population level (but not at the individual player level) which cannot be understood by the NE concept but are successfully explained by the empirical datainspired CR mechanism. As far as the action marginal distributions of individual players are concerned, the CR strategy is indistinguishable from the NE mixed strategy, yet it is capable of bringing higher payoffs to the players if its parameters are optimized and all players adopt the same CR strategy. This simple conditional response strategy, with the winstay loseshift strategy being a special case, appears to be psychologically plausible for human subjects with bounded rationality^{46,47}. For more complicated game payoff matrices, we can generalize the conditional response model accordingly by introducing a larger set of CR parameters (see Supplementary Notes online). It should be very interesting to reanalyze many existing laboratory experimental data^{9,29,35,48,49,50,51} using this extended model. Figure 3 also reveals that the empirical CR parameters and the socialstate cycling frequency change with the payoff parameter a. In a following paper we will study the effect of the payoff parameter a to the individual and populationlevel behaviors in more detail^{52}.
The CR model as a simple model of decisionmaking under uncertainty deserves to be fully explored. For example, different players may have different CR transition parameters and these transition parameters may change with time constantly as a result of learning. We find the cycling frequency is not sensitive to population size N at given CR parameters (see Supplementary Fig. S2 online); and the cycling frequency is nonzero even for symmetric CR parameters (i.e., W_{+}/W_{−} = T_{+}/T_{−} = L_{+}/L_{−} = 1), as long as W_{0} ≠ L_{0} (see Supplementary Fig. S3 online). The optimization issue of CR parameters is left out in this work. We will investigate whether an optimal CR strategy is achievable through simple stochastic learning rules^{42,43,45}. The effects of memory length^{53} and population size to the optimal CR strategies also need to be thoroughly studied. On the more biological side, whether conditional response is a basic decisionmaking mechanism of the human brain or just a consequence of more fundamental neural mechanisms is a challenging question for future studies.
Methods
Experiment
The experiment was approved by the Experimental Social Science Laboratory of Zhejiang University and performed at Zhejiang University in the period of December 2010 to March 2014. The corresponding author confirms that this experiment was performed in accordance with the approved social experiments guidelines and regulations. A total number of 360 undergraduate and graduate students of Zhejiang University volunteered to serve as the human subjects of this experiment. These students were openly recruited through a web registration system. Female students were slightly more enthusiastic than male students in registering as candidate human subjects of our experiment. Since we sampled students uniformly at random from the candidate list, more female students were recruited than male students (among the 360 students, the female versus male ratio is 217:143). Informed consent was obtained from all the participanting human subjects.
The 360 human subjects (referred to as players in this work) were distributed into 60 populations of equal size N = 6. The six players of each population carried one experimental session by playing the RPS game for 300 rounds with fixed payoff parameter a, whose value is chosen from {1.1, 2, 4, 9, 100}. During the game process the players sited separately in a classroom, each of which facing a computer screen. They were not allowed to communicate with each other during the whole experimental session. Written instructions were handed out to each player and the rules of the experiment were also orally explained by an experimental instructor. The rules of the experimental session are as follows:

i
Each player plays the RPS game repeatedly with the same other five players.

ii
Each player earns virtual points during the experimental session according to the payoff matrix shown in the written instruction. These virtual points are then exchanged into RMB as a reward to the player, plus an additional 5 RMB as showup fee.

iii
In each game round, the six players of each group are randomly matched by a computer program to form three pairs and each player competes only with the pair opponent.

iv
Each player has at most 40 seconds in one game round to make a choice among the three candidate actions “Rock”, “Paper” and “Scissors”. If this time runs out, the player has to make a choice immediately (the experimental instructor will loudly urge these players to do so). After a choice has been made it can not be changed.
Before the start of the actual experimental session, the player were asked to answer four questions to ensure that they understand completely the rules of the experimental session. These four questions are: (1) If you choose “Rock” and your opponent chooses “Scissors”, how many virtual points will you earn? (2) If you choose “Rock” and your opponent chooses also “Rock”, how many virtual points will you earn? (3) If you choose “Scissors” and your opponent chooses “Rock”, how many virtual points will you earn? (4) Do you know that at each game round you will play with a randomly chosen opponent from your group (yes/no)?
During the experimental session, the computer screen of each player will show an information window and a decision window. The window on the left of the computer screen is the information window. The upper panel of this information window shows the current game round, the time limit (40 seconds) of making a choice and the time left to make a choice. The color of this upper panel turns to green at the start of each game round. The color will change to yellow if the player does not make a choice within 20 seconds. The color will change to red if the decision time runs out (and then the experimental instructor will loudly urge the players to make a choice immediately). The color will change to blue if a choice has been made by the player. After all the players of the group have made their decisions, the lower panel of the information window will show the player's own choice, the opponent's choice and the player's own payoff in this game round. The player's own accumulated payoff is also shown. The players are asked to record their choices of each round on the record sheet (Rock as R, Paper as P and Scissors as S).
The window on the right of the computer screen is the decision window. It is activated only after all the players of the group have made their choices. The upper panel of this decision window lists the current game round, while the lower panel lists the three candidate actions “Rock”, “Scissors”, “Paper” horizontally from left to right. The player can make a choice by clicking on the corresponding action names. After a choice has been made by the player, the decision window becomes inactive until the next game round starts.
The reward in RMB for each player is determined by the following formula. Suppose a player i earns x_{i} virtual points in the whole experimental session, the total reward y_{i} in RMB for this player is then given by
where r is the exchange rate between virtual point and RMB. According to the mixedstrategy Nash equilibrium, the expected payoff of each player in one game round is (1 + a)/3. Therefore we set the exchange rate to be r = 0.45/(1 + a) to ensure that, under the mixedstrategy NE assumption, the expected total earning in RMB for a player will be 50 RMB irrespective of the particular experimental session. The value of the payoff parameter a, the numerical value of r and the abovementioned reward formula were listed in the written instruction and also orally mentioned by the experimental instructor at the instruction phase of the experiment.
Rotation angle computation
Consider a transition from one social state s = (n_{R}, n_{P}, n_{S}) at game round t to another social state at game round (t + 1), if at least one of the two social states coincides with the centroid c_{0} of the social state plane, or the three points s, and c_{0} lie on a straight line, then the transition is not regarded as a rotation around c_{0} and the rotation angle θ = 0. In all the other cases, the transition is regarded as a rotation around c_{0} and the rotation angle is computed through
where acos(x) ∈ [0, π) is the inverse cosine function and if (counterclockwise rotation around c_{0}) and if otherwise (clockwise rotation around c_{0}).
Statistical Analysis
Statistical analyses, including Wilcoxon signedrank test and Spearman's rank correlation test, were performed by using stata 12.0 (Stata, College Station, TX).
Transition matrix of the conditional response model
For the conditional response model, the transition probability M_{cr}[s′s] from the social state s ≡ (n_{R}, n_{P}, n_{S}) at time t to the social state at time (t + 1) is expressed as:
References
Sinervo, B. & Lively, C. The rockpaperscissors game and the evolution of alternative male strategies. Nature 380, 240–243 (1996).
Kerr, B., Riley, M. A., Feldman, M. W. & Bohannan, B. J. M. Local dispersal promotes biodiversity in a reallife game of rockpaperscissors. Nature 418, 171–174 (2002).
Semmann, D., Krambeck, H.J. & Milinski, M. Volunteering leads to rockpaperscissors dynamics in a public goods game. Nature 425, 390–393 (2003).
Lee, D., McGreevy, B. P. & Barraclough, D. J. Learning and decision making in monkeys during a rockpaperscissors game. Cogn. Brain Res. 25, 416–430 (2005).
Reichenbach, T., Mobilia, M. & Frey, E. Mobility promotes and jeopardizes biodiversity in rockpaperscissors games. Nature 448, 1046–1049 (2007).
Allesina, S. & Levine, J. M. A competitive network theory of species diversity. Proc. Natl. Acad. Sci. USA 108, 5638–5642 (2011).
Maskin, E. & Tirole, J. A theory of dynamic oligopoly, ii: Price competition, kinked demand curves and edgeworth cycles. Econometr. 56, 571–599 (1988).
Cason, T. N. & Friedman, D. Buyer search and price dispersion: a laboratory study. J. Econ. Theory 112, 232–260 (2003).
Hoffman, M., Suetens, S., Nowak, M. A. & Gneezy, U. An experimental test of nash equilibrium versus evolutionary stability. In: Proc. 4th World Cong. Game Theory Soc. (GAMES 2012), session 145, paper 1 (Istanbul, Turkey, 2012) (Data of access: 05/02/2014).
Nash, J. F. Equilibrium points in nperson games. Proc. Natl. Acad. Sci. USA 36, 48–49 (1950).
Osborne, M. J. & Rubinstein, A. A Course in Game Theory (MIT Press, New York, 1994).
Taylor, P. D. & Jonker, L. B. Evolutionarily stable strategies and game dynamics. Math. Biosci. 40, 145–156 (1978).
Maynard Smith, J. & Price, G. R. The logic of animal conflict. Nature 246, 15–18 (1973).
Maynard Smith, J. Evolution and the Theory of Games (Cambridge University Press, Cambridge, 1982).
Axelrod, R. The Evolution of Cooperation (Basic Books, New York, 1984).
Nowak, M. A. & Sigmund, K. Evolutionary dynamics of biological games. Science 303, 793–799 (2004).
Szabó, G. & Fáth, G. Evolutionary games on graphs. Phys. Rep. 446, 97–216 (2007).
Sandholm, W. M. Population Games and Evolutionary Dynamics (MIT Press, New York, 2010).
Claussen, J. C. & Traulsen, A. Cyclic dominance and biodiversity in wellmixed populations. Phys. Rev. Lett. 100, 058104 (2008).
Roca, C. P., Cuesta, J. A. & Sánchez, A. Evolutionary game theory: Temporal and spatial effects beyond replicator dynamics. Phys. Life Rev. 6, 208–249 (2009).
Andrae, B., Cremer, J., Reichenbach, T. & Frey, E. Entropy production of cyclic population dynamics. Phys. Rev. Lett. 104, 218102 (2010).
Matsui, A. Best response dynamics and socially stable strategies. J. Econ. Theory 57, 343–362 (1992).
Hopkins, E. A note on best response dynamics. Gam. Econ. Behav. 29, 138–150 (1999).
Blume, L. E. The statistical mechanics of strategic interation. Gam. Econ. Behav. 5, 387–424 (1993).
Hommes, C. H. & Ochea, M. I. Multiple equilibria and limit cycles in evolutionary games with logit dynamics. Gam. Econ. Behav. 74, 434–441 (2012).
Xu, B. & Wang, Z. Evolutionary dynamical patterns of ‘coyness and philandering’: Evidence from experimental economics. In: Proc. 8th Int. Conf. Compl. Sys. 1313–1326 (Boston, MA, USA, 2011) (Data of access: 15/03/2014).
Xu, B. & Wang, Z. Test maxent in social strategy transitions with experimental twoperson constant sum 2 × 2 games. Resul. Phys. 2, 127–134 (2012).
Xu, B., Zhou, H.J. & Wang, Z. Cycle frequency in standard rockpaperscissors games: Evidence from experimental economics. Physica A 392, 4997–5005 (2013).
Cason, T. N., Friedman, D. & Hopkins, E. Cycles and instability in a rockpaperscissors population game: A continuous time experiment. Rev. Econ. Stud. 81, 112–136 (2014).
Castellano, C., Fortunato, S. & Loreto, V. Statistical physics of social dynamics. Rev. Mod. Phys. 81, 591–646 (2009).
Huang, J.P. Econophysics (Higher Education Press, Beijing, 2013).
Ao, P. Emerging of stochastic dynamical equalities and steady state thermodynamics from darwinian dynamics. Commun. Theor. Phys. 49, 1073–1090 (2008).
Ao, P., Chen, T.Q. & Shi, J.H. Dynamical decomposition of markov processes without detailed balance. Chin. Phys. Lett. 30, 070201 (2013).
Zhou, T., Han, X.P. & Wang, B.H. Towards the understanding of human dynamics. In: Burguete, M. & Lam, L. (eds.) Science Matters: Humanities as Complex Systems 207–233 (World Scientific, Singapore, 2008).
Frey, S. & Goldstone, R. L. Cyclic game dynamics driven by iterated reasoning. PLoS ONE 8, e56416 (2013).
Kemeny, J. G. & Snell, J. L. Finite Markov Chains; with a New Appendix “Generalization of a Fundamental Matrix” (SpringerVerlag, New York, 1983).
Kraines, D. & Kraines, V. Learning to cooperate with pavlov: an adaptive strategy for the iterated prisoner's dilemma with noise. Theory Decis. 35, 107–150 (1993).
Nowak, M. & Sigmund, K. A strategy of winstay, loseshift that outperforms titfortat in the prisoner's dilemma game. Nature 364, 56–58 (1993).
Wedekind, C. & Milinski, M. Human cooperation in the simultaneous and the alternating prisoner's dilemma: Pavlov versus generous titfortat. Proc. Natl. Acad. Sci. USA 93, 2686–2689 (1996).
Posch, M. Winstay, loseshift strategies for repeated games–memory length, aspiration levels and noise. J. Theor. Biol. 198, 183–195 (1999).
Glimcher, P. W., Camerer, C. F., Fehr, E. & Poldrack, R. A. (eds.). Neuroeconomics: Decision Making and the Brain (Academic Press, London, 2009).
Börgers, T. & Sarin, R. Learning through reinforcement and replicator dynamics. J. Econ. Theory 77, 1–14 (1997).
Posch, M. Cycling in a stochastic learning algorithm for normal form games. J. Evol. Econ. 7, 193–207 (1997).
Galla, T. Intrinsic noise in game dynamical learning. Phys. Rev. Lett. 103, 198702 (2009).
Janacsek, K. & Nemeth, D. Predicting the future: From implicit learning to consolidation. Int. J. Psychophysiol. 83, 213–221 (2012).
Camerer, C. Behavioral economics: Reunifying psychology and economics. Proc. Natl. Acad. Sci. USA 96, 10575–10577 (1999).
Camerer, C. Behavioral game theory: Experiments in strategic interaction (Princeton University Press, Princeton, NJ, 2003).
Berninghaus, S. K., Ehrhart, K.M. & Keser, C. Continuoustime strategy selection in linear population games. Exper. Econ. 2, 41–57 (1999).
Traulsen, A., Semmann, D., Sommerfeld, R. D., Krambeck, H.J. & Milinski, M. Human strategy updating in evolutionary games. Proc. Natl. Acad. Sci. USA 107, 2962–2966 (2010).
GraciaLázaro, C. et al. Heterogeneous networks do not promote cooperation when humans play a prisoner's dilemma. Proc. Natl. Acad. Sci. USA 109, 12922–12926 (2012).
Chmura, T., Goerg, S. J. & Selten, R. Generalized impulse balance: An experimental test for a class of 3 × 3 games. Rev. Behav. Econ. 1, 27–53 (2014).
Wang, Z. & Xu, B. Incentive and stability in the RockPaperScissors game: An experimental investigation. eprint arXiv/1407.1170 (2014).
Press, W. H. & Dyson, F. J. Iterated prisoner's dilemma contains strategies that dominate any evolutionary opponent. Proc. Natl. Acad. Sci. USA 109, 10409–10413 (2012).
Acknowledgements
We thank Professors WeiDong Luo, ZhongCan OuYang and BingSong Zou for support and encouragement. ZW and BX thank AnPing Sun and ZunFeng Wang for experimental assistance and HJZ thanks Angelo Valleriani, Erik Aurell, Ping Ao and JiPing Huang for helpful comments on the manuscript. ZW and BX were supported by the Fundamental Research Funds for the Central Universities (SSEYI2014Z), the State Key Laboratory for Theoretical Physics (Y3KF261CJ1) and the Philosophy and Social Sciences Planning Project of Zhejiang Province (13NDJC095YB); HJZ was supported by the National Basic Research Program of China (2013CB932804), the Knowledge Innovation Program of Chinese Academy of Sciences (KJCX2EWJ02) and the National Science Foundation of China (11121403, 11225526).
Author information
Authors and Affiliations
Contributions
Z.W. and B.X. contributed equally to this work. Z.W., B.X. designed and performed experiment; B.X. measured conditional response transition probabilities; H.J.Z. developed analytical and numerical methods; B.X., Z.W., H.J.Z. analyzed and interpreted data; H.J.Z., B.X. wrote the paper.
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Electronic supplementary material
Supplementary Information
SIv16Zhou
Rights and permissions
This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
About this article
Cite this article
Wang, Z., Xu, B. & Zhou, HJ. Social cycling and conditional responses in the RockPaperScissors game. Sci Rep 4, 5830 (2014). https://doi.org/10.1038/srep05830
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/srep05830
This article is cited by

Variability in competitive decisionmaking speed and quality against exploiting and exploitative opponents
Scientific Reports (2021)

Periodic Attractor in the Discrete Time BestResponse Dynamics of the RockPaperScissors Game
Dynamic Games and Applications (2021)

MultiAI competing and winning against humans in iterated RockPaperScissors game
Scientific Reports (2020)

Properties of a novel stochastic rock–paper–scissors dynamics
Journal of Applied Mathematics and Computing (2020)

The Impact of Competition on Analysts’ Forecasts: A Simple AgentBased Model
Journal of Systems Science and Complexity (2020)
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.