Literature DB >> 30069646

On the distribution of the number of internal equilibria in random evolutionary games.

Manh Hong Duong1, Hoang Minh Tran2, The Anh Han3.   

Abstract

The analysis of equilibrium points is of great importance in evolutionary game theory with numerous practical ramifications in ecology, population genetics, social sciences, economics and computer science. In contrast to previous analytical approaches which primarily focus on computing the expected number of internal equilibria, in this paper we study the distribution of the number of internal equilibria in a multi-player two-strategy random evolutionary game. We derive for the first time a closed formula for the probability that the game has a certain number of internal equilibria, for both normal and uniform distributions of the game payoff entries. In addition, using Descartes' rule of signs and combinatorial methods, we provide several universal upper and lower bound estimates for this probability, which are independent of the underlying payoff distribution. We also compare our analytical results with those obtained from extensive numerical simulations. Many results of this paper are applicable to a wider class of random polynomials that are not necessarily from evolutionary games.

Entities:  

Keywords:  Distributions of equilibria; Evolutionary game theory; Multi-player games; Random games; Random polynomials; Replicator dynamics

Mesh:

Year:  2018        PMID: 30069646      PMCID: PMC6437138          DOI: 10.1007/s00285-018-1276-0

Source DB:  PubMed          Journal:  J Math Biol        ISSN: 0303-6812            Impact factor:   2.259


Introduction

Motivation

Evolutionary Game Theory (EGT) (Maynard Smith and Price 1973) has become one of the most diverse and far reaching theories in biology finding its applications in a plethora of disciplines such as ecology, population genetics, social sciences, economics and computer science (Maynard Smith 1982; Axelrod 1984; Hofbauer and Sigmund 1998; Nowak 2006; Broom and Rychtář 2013; Perc and Szolnoki 2010; Sandholm 2010; Han et al. 2017), see also recent reviews (Wang et al. 2016; Perc et al. 2017). For example, in economics, EGT has been employed to make predictions in situations where traditional assumptions about agents’ rationality and knowledge may not be justified (Friedman 1998; Sandholm 2010). In computer science, EGT has been used extensively to model dynamics and emergent behaviour in multiagent systems (Helbing et al. 2015; Tuyls and Parsons 2007; Han 2013). Furthermore, EGT has provided explanations for the emergence and stability of cooperative behaviours which is one of the most well-studied and challenging interdisciplinary problems in science (Pennisi 2005; Hofbauer and Sigmund 1998; Nowak 2006). A particularly important subclass in EGT is random evolutionary games in which the payoff entries are random variables. They are useful to model social and biological systems in which very limited information is available, or where the environment changes so rapidly and frequently that one cannot describe the payoffs of their inhabitants’ interactions (May 2001; Fudenberg and Harris 1992; Han et al. 2012; Gross et al. 2009; Galla and Farmer 2013). Similar to the foundational concept of Nash equilibrium in classical game theory (Nash 1950), the analysis of equilibrium points is of great importance in EGT. It provides essential understanding of complexity in a dynamical system, such as its behavioural, cultural or biological diversity (Haigh 1988, 1990; Broom et al. 1997; Broom 2003; Gokhale and Traulsen 2010, 2014; Han et al. 2012; Duong and Han 2015, 2016; Broom and Rychtář 2016). A large body of literature has analysed the number of equilibria, their stability and attainability in concrete strategic scenarios such as the public goods game and its variants, see for example Broom et al. (1997), Broom (2000), Pacheco et al. (2009), Souza et al. (2009), Peña (2012), Peña et al. (2014) and Sasaki et al. (2015). However, despite their importance, equilibrium properties in random games are far less understood with, to the best of our knowledge, only a few recent efforts (Gokhale and Traulsen 2010, 2014; Han et al. 2012; Galla and Farmer 2013; Duong and Han 2015, 2016; Broom and Rychtář 2016). One of the most challenging problems in the study of equilibrium properties in random games is to characterise the distribution of the number of equilibria (Gokhale and Traulsen 2010; Han et al. 2012):This question has been studied in the literature to some extent. For example, in Gokhale and Traulsen (2010, 2014) and Han et al. (2012), the authors studied this question with a small number of players () and only focused on the probability of attaining the maximal number of equilibrium points, i.e. , where () is the probability that a d-player game with two strategies has exactly m internal equilibria. These works use a direct approach by analytically solving a polynomial equation, expressing the positivity of its zeros as domains of conditions for the coefficients and then integrating over these domains to obtain the corresponding probabilities. However, it is impossible to extend this approach to games with a large or arbitrary number of players as in general, a polynomial of degree five or higher is not analytically solvable (Abel 1824). In more recent works (Duong and Han 2015, 2016; Duong et al. 2017), we have established the links between random evolutionary games, random polynomial theory (Edelman and Kostlan 1995) and classical polynomial theory (particularly Legendre polynomials), employing techniques from the latter to study the expected number of internal equilibria, E. More specifically, we provided closed form formulas for E, characterised its asymptotic limits as the number of players in the game tends to infinity and investigated the effect of correlation in the case of correlated payoff entries. On the one hand, E offers useful information regarding the macroscopic, average behaviour of the number of internal equilibria a dynamical system might have. On the other hand, E cannot provide the level of complexity or the number of different states of biodiversity that will occur in the system. In these situations, details about how the number of internal equilibrium points distributed is required. Furthermore, as E can actually be derived from using the formula , a closed form formula for would make it possible to compute E for any d, hence filling in the gap in the literature on computing E for large d (. Therefore, it is necessary to estimate . What is the distribution of the number of (internal) equilibria in a d-player random evolutionary game and how can we compute it?

Summary of main results

In this paper, we address the above question by providing a closed-form formula for the probability (). Our approach is based on the links between random polynomial theory and random evolutionary game theory established in our previous work (Duong and Han 2015, 2016). That is, an internal equilibrium in a d-player game with two strategies can be found by solving the following polynomial equation (detailed derivation in Sect. 2),where , with and being random variables representing the entries of the game payoff matrix. We now summarise the main results of this paper. Detailed derivations and proofs will be given in subsequent sections. The first main result is an explicit formula for the probability distribution of the number of internal equilibria.

Theorem 1

(The distribution of the number of internal equilibria in a d-player two-strategy random evolutionary game) Suppose that the coefficients in (1) are either normally distributed, uniformly distributed or the difference of uniformly distributed random variables. The probability that a d-player two-strategy random evolutionary game has m, , internal equilibria, is given bywhere are given in (13), (14) and (15), respectively. This theorem, which is stated in detail in Theorem 4 in Sect. 3, is derived from a more general theorem, Theorem 3, where we provide explicit formulas for the probability that a random polynomial of degree n has m () positive, 2k () complex and negative roots. Note that results from Theorem 3 are applicable to a wider class of general random polynomials, i.e. beyond those derived from evolutionary random games considered in this work. Theorem 1 is theoretically interesting and can be used to compute , for small d. We use it to compute all the probabilities , , for d up to 5, and compare the results with those obtained through extensive numerical simulations (for validation). However, when d is larger it becomes computationally expensive to compute these probabilities using formula (2) because one needs to calculate all the probabilities , , which are complex multiple integrals. To overcome this issue, in Sect. 5, we develop our second main result, Theorem 2 below, which offers simpler explicit estimates of in terms of d and m. The main idea in developing this result is employing the symmetry of the coefficients . Specifically, we consider two casesfor all and for some . Note here that Case 1 is an instance of Case 2 when and can be satisfied when and are exchangeable (see Lemma 1 below). Interestingly, the symmetry of allows us to obtain a much simpler treatment. The general case allows us to move beyond the exchangeability condition capturing the fact that different strategies might have different payoff properties.

Theorem 2

We have the following upper-bound estimate for where if , in this case the sum on the right hand side of  (3) can be computed explicitly in terms of m and d. For the general case, it can be computed explicitly according to Theorem 7. The estimate (3) has several useful implications, leading to explicit bounds for and as well as the following assertions: For : and ; For : . This theorem is a summary of Theorems 6, 7 and 8 in Sect. 4 that are derived using Descartes’ rule of signs and combinatorial methods. We note that results of the aforementioned theorems are applicable to a wider class of random polynomials that are not necessarily from random games.

Organisation of the paper

The rest of the paper is organised as follows. In Sect. 2, we recall and summarise the replicator dynamics for multi-player two-strategy games. The main contributions of this paper and the detailed analysis of the main results described above will be presented in subsequent sections. Section 3 is devoted to the proof of Theorem 1 on the probability distribution. The proof of Theorem 2 will be given in Sect. 4. In Sect. 5 we show some numerical simulations to demonstrate analytical results. In Sect. 6, further discussions are given. Finally, Appendix 1 contains proofs of technical results from previous sections.

Replicator dynamics

A fundamental model of evolutionary game theory is replicator dynamics (Taylor and Jonker 1978; Zeeman 1980; Hofbauer and Sigmund 1998; Schuster and Sigmund 1983; Nowak 2006), describing that whenever a strategy has a fitness larger than the average fitness of the population, it is expected to spread. For the sake of completeness, below we derive the replicator dynamics for multi-player two-strategy games. Consider an infinitely large population with two strategies, A and B. Let x, , be the frequency of strategy A. The frequency of strategy B is thus . The interaction of the individuals in the population is in randomly selected groups of d participants, that is, they play and obtain their fitness from d-player games. The game is defined through a -dimensional payoff matrix (Gokhale and Traulsen 2010), as follows. Let (respectively, ) be the payoff that an A-strategist (respectively, a B-strategist) obtained when playing with a group of players that consists of k A-strategists. In this paper, we consider symmetric games where the payoffs do not depend on the ordering of the players. Asymmetric games will be studied in a forthcoming paper. In the symmetric case, the probability that an A strategist interacts with k other A strategists in a group of size isThus, the average payoffs of A and B are, respectivelyThe replicator equation of a d-player two-strategy game is given by (Hofbauer and Sigmund 1998; Sigmund 2010; Gokhale and Traulsen 2010)Since and are two trivial equilibrium points, we focus only on internal ones, i.e. . They satisfy the condition that the fitnesses of both strategies are the same, i.e. , which gives rise towhere . Using the transformation , with , dividing the left hand side of the above equation by we obtain the following polynomial equation for yNote that this equation can also be derived from the definition of an evolutionarily stable strategy (ESS), an important concept in EGT (Maynard Smith 1982), see e.g., Broom et al. (1997). Note however that, when moving to random evolutionary games with more than two strategies, the conditions for ESS are not the same as for those of stable equilibrium points of replicator dynamics. As in Gokhale and Traulsen (2010), Duong and Han (2015, 2016), we are interested in random games where and (thus ), for , are random variables. In Sect. 3 where we provide estimates for the number of internal equilibria in a d-player two-strategy game, we will use the information on the symmetry of . The following lemma gives a necessary condition to determine when the difference of two random variables is symmetrically distributed.

Lemma 1

(Duong et al. 2017, Lemma 3.5) Let X and Y be two exchangeable random variables, i.e. their joint probability distribution is symmetric, . Then is symmetrically distributed about 0, i.e., its probability distribution satisfies . In addition, if X and Y are i.i.d then they are exchangeable. For the sake of completeness, the proof of this Lemma is provided in Sect. 1.

The distribution of the number of positive zeros of random polynomials and applications to EGT

This section focuses on deriving the distribution of the number of internal equilibria of a d-player two-strategy random evolutionary game. We recall that an internal equilibria is a real and positive zero of the polynomial P(y) in (5). We denote by the number of positive zeros of this polynomial. For a given m, , we need to compute the probability that . To this end, we first adapt a method introduced in Zaporozhets (2006) (see also Butez and Zeitouni 2017; Götze et al. 2017 for its applications to other problems) to establish a formula to compute the probability that a general random polynomial has a given number of real and positive zeros. Then we apply the general theory to the polynomial P.

The distribution of the number of positive zeros of a random polynomial

Consider a general random polynomialWe use the following notations for the elementary symmetric polynomialsand denote bythe Vandermonde determinant.

Theorem 3

Assume that the random variables have a joint density . Let and . The probability that has m positive, 2k complex and negative zeros is given bywhereAs consequences, The probability that has m positive zeros is In particular, the probability that has the maximal number of positive zeros is where

Proof

The reference (Zaporozhets 2006, Theorem 1) provides a formula to compute the probability that the polynomial has real and 2k complex roots. In the present paper, we need to distinguish between positive and negative real zeros. We now sketch and adapt the proof of Theorem 1 of Zaporozhets (2006) to obtain the formula (9) for the probability that the polynomial has m positive, 2k complex and negative roots. Consider a -dimensional vector space of polynomials of the formand a measure on this space defined as the integral of the differential formOur goal is to find where is the set of polynomials having m positive, 2k complex and negative roots. Let . Denote all zeros of Q aswhereTo find we need to integrate the differential form (12) over the set . The key idea in the proof of Theorem 1 of Zaporozhets (2006) is to make a change of coordinates , with , and find dQ in the new coordinates. The derivation of the following formula is carried out in detail in Zaporozhets (2006):Now we integrate this equation over all polynomials Q that have m positive zeros, negative zeros and k complex zeros in the upper half-plane. Since there are m! permutations of the positive zeros, permutations of the negative zeros, and k! permutations of the complex zeros, after integrating each polynomial in the left-hand side will occur times. Hence the integral of the left-hand side is equal to . The integral on the right-hand side equalshence the assertion (9) follows.

The distribution of the number of internal equilibria

Next we apply Theorem 3 to compute the probability that a random evolutionary game has m, , internal equilibria. We derive formulas for the three most common cases (Han et al. 2012):The main result of this section is the following theorem (cf. Theorem 2). are i.i.d. standard normally distributed, are i.i.d. uniformly distributed with the common distribution , and are i.i.d. uniformly distributed with the common distribution .

Theorem 4

The probability that a d-player two-strategy random evolutionary game has m () internal equilibria iswhere is given below for each of the cases above: – For the case (C1)where , for , and are given in (10)–(11) and . – For the case (C2)– For the case (C3)In particular, the probability that a d-player two-strategy random evolutionary game has the maximal number of internal equilibria is:Note that in formulas (16)–(18) above for the case (C1) for the case (C2) for the case (C3) (1) Since are i.i.d. standard normally distributed, the joint distribution of is given bywhere and is the covariance matrixTherefore,where . Using the following formula for moments of a normal distribution,we computeApplying Theorem 3 to the polynomial P given in (5) and using the above identity we obtainwhich is the desired equality (13) by definition of and . (2) Now since are i.i.d. uniformly distributed with the common distribution , the joint distribution ofis given byTherefore,Since if and only if for all , i.e., if and only ifwe have (for simplicity of notation, in the subsequent computations we shorten by )Therefore,Similarly as in the normal case, using this identity and applying Theorem 3 we obtain(3) Now we assume that and are i.i.d. uniformly distributed with the common distribution . Since , its probability density is given byThe probability density of isand the joint distribution of is given byThereforeWe computewhere for . Therefore,

Corollary 1

The expected numbers of internal equilibria and stable internal equilibria, E(d) and SE(d), respectively, of a d-player two-strategy game, are given by Note that this formula for E(d) is applicable for non-normal distributions, which is in contrast to the method used in previous works (Duong and Han 2015, 2016) that can only be used for normal distributions. The second part, i.e. the formula for the expected number of stable equilibrium points, was obtained based on the following property of stable equilibria in multi-player two-strategy evolutionary games, as shown in Han et al. (2012, Theorem 3): .

Remark 1

In Theorem 4 for the case (C1), the assumption that ’s are standard normal distributions, i.e. having variance 1, is just for simplicity. Suppose that ’s are normal distributions with mean 0 and variance . We show that the probability , for , does not depend on . In this case, the formula for p is given by (19) but with being replaced by . To indicate its dependence on , we write . We use a change of variable . Thenfrom which we deduce that does not depend on . Similarly for the other cases, the uniform interval can be for some . For illustration of the application of Theorem 4, the following examples show explicit calculations for and 4 for the case of normal distributions, i.e. (C1). Further numerical results for and also for other distributions, i.e. (C2) and (C3), are provided in Fig. 1. The integrals in these examples were computed using Mathematica.
Fig. 1

Numerical versus simulation calculations of the probability of having a concrete number (m) of internal equilibria, , for different values of d. The payoff entries and were drawn from a normal distribution with variance 1 and mean 0 (GD) and from a standard uniform distribution (UD2). We also study the case where itself is drawn from a standard uniform distribution (UD1). Results are obtained from analytical formulas (Theorem 2) (a) and are based on sampling payoff matrices (b) where payoff entries are drawn from the corresponding distributions. Analytical and simulations results are in accordance with each other. All results are obtained using Mathematica

Examples for

Example 1

(Three-player two-strategy games: ) (1) One internal equilibria: . We haveSubstituting these values into (13) we obtain the probability that a three-player two-strategy evolutionary game has 1 internal equilibria(2) Two internal equilibria: . We haveThe probability that a three-player two-strategy evolutionary game has 2 internal equilibria is(3) No internal equilibria: the probability that a three-player two-strategy evolutionary game has no internal equilibria is

Example 2

(Four-player two-strategy games: ) (1) One internal equilibria: . We first compute . In this case,Substituting these into (13) we getNext we compute . In this case,Substituting these into (13) yieldsTherefore, we obtain that(2) Two internal equilibria: The probability that a four-player two-strategy evolutionary game has 2 internal equilibria is(3) Three internal equilibria: The probability that a four-player two-strategy evolutionary game has 3 internal equilibria is(4) No internal equilibria: the probability that a four-player two-strategy evolutionary game has no internal equilibria is: .

Universal estimates for

In Sect. 3, we have derived closed-form formulas for the probability distributions of the number of internal equilibria. However, it is computationally expensive to compute these probabilities since it involves complex multiple-dimensional integrals. In this section, using Descartes’ rule of signs and combinatorial techniques, we provide universal estimates for . Descartes’ rule of signs is a technique for determining an upper bound on the number of positive real roots of a polynomial in terms of the number of sign changes in the sequence formed by its coefficients. This rule has been applied to random polynomials before in the literature (Bloch and Pólya 1932); however this paper only obtained estimates for the expected number of zeros of a random polynomial.

Theorem 5

(Descartes’ rule of signs, see e.g., Curtiss 1918) Consider a polynomial of degree n, with . Let v be the number of variations in the sign of the coefficients and be the number of real positive zeros. Then is an even non-negative integer. We recall that an internal equilibrium of a d-player two-strategy game is a positive root of the polynomial P given in (5). We will apply Descartes’ rule of signs to find an upper bound for the probability that a random polynomial has a certain number of positive roots. This is a problem that is of interest in its own right and may have applications elsewhere; therefore we will first study this problem for a general random polynomial of the formand then apply it to the polynomial P. It turns out that the symmetry of will be the key: the asymmetric case requires completely different treatment from the symmetric one.

Estimates of : symmetric case

We first consider the case where the coefficients in (22) are symmetrically distributed. The main result of this section will be Theorem 6 that provides several upper and lower bounds for the probability that a d-player two strategy game has m internal equilibria. Before stating Theorem 6, we need the following auxiliary lemmas.

Proposition 1

Suppose that the coefficients in the polynomial (22) are i.i.d. and symmetrically distributed. Let , be the probability that the sequence of coefficients has k changes of signs. Then See Appendix 2. The next two lemmas on the sum of binomial coefficients will be used later on.

Lemma 2

Let be positive integers. Then it holds thatwhere it is understood that if . In particular, for , we get See Appendix 3. The following lemma provides estimates on the sum of the first k binomial coefficients.

Lemma 3

Let n and be positive integers. We have the following estimates (MacWilliams and Sloane 1977, Lemma 8 and Corollary 9, Chapter 10; Gottlieb et al. 2012)where and H is the binary entropy functionwhere is taken to be 0. In addition, if is even and , we also have the following estimate (Lovász et al. 2003, Lemma 3.8.2) We now apply Proposition 1 and Lemmas 2 and 3 to derive estimates for the probability that a d-player two-strategy evolutionary game has a certain number of internal equilibria. The main theorem of this section is the following.

Theorem 6

Suppose that the coefficients in (5) are symmetrically distributed. Let be the probability that the d-player two-strategy random game has m internal equilibria. Then the following assertions hold Upper-bound for , for all , As consequences, for all , , and . In addition, if is even and then Lower-bound for and : For : . For : . (a) This part is a combination of Decartes’ rule of signs, Proposition 1 and Lemmas 2 and 3. In fact, as a consequence of this rule and by Proposition 1, we havewhich is the inequality part in (29). Next, applying Lemma 2 for and and then Lemma 3, we obtainThis proves the equality part in (29) and (30). As a result, the estimate for all is followed from (29) and (24); the estimates and are special cases of (29) for and , respectively. Finally, the estimate (31) is a consequence of (29) and (28). (b) It follows from Decartes’ rule of signs and Proposition 1 that(c) For : from parts (a) and (b) we havewhich implies that as claimed. (d) Finally, for : also from parts (a) and (b) we getso . This finishes the proof of Theorem 6.

Remark 2

Note that in Theorem 6 we only assume that are symmetrically distributed but do not require that they are normal distributions. When are normal distributions, we have derived (Duong and Han 2015, 2016) a closed formula for the expected number E(d) of internal equilibria, which can be computed efficiently for large d. Since , we have for all . Therefore, when are normal, we obtain an upper bound for as the minimum between E(d) / m and the bound obtained in Theorem 6. The comparison of the new bounds with E(d) / m in Fig. 2 shows that the new ones do better for m closer to 0 or but worse for intermediate m (i.e. closer to ).
Fig. 2

Comparison of the new upper bounds of derived in Theorem 6 with that of E(d) / m: a for the bound in (36) and b for the bound in (37). Black areas indicate when the former ones are better and the grey areas otherwise. Clearly the bound in (a) is stricter/better than that of (b). For small d, the new bounds are better. When d is sufficiently large, we observe that for any d, the new bounds are worse than E(d) / m when m is intermediate while better otherwise. Overall, this comparison indicates which formulas should be used to obtain a stricter upper bound of

Estimates of : general case

In the proof of Proposition 1 the assumption that are symmetrically distributed is crucial. In that case, all the binary sequences constructed are equally distributed, resulting in a compact formula for . However, when are not symmetrically distributed, those binary sequences are no longer equally distributed. Thus computing becomes much more intricate. We now consider the general case whereNote that the general case allows us to move beyond the usual assumption in the analysis of random evolutionary games that all payoff entries ’s and ’s have the same probability distribution resulting in (see Lemma 1). In the general case it only requires that all ’s have the same distribution and all ’s have the same distribution, capturing the fact that different strategies, i.e. A and B in Sect. 2, might have different payoff properties (e.g., defectors always have a larger payoff than cooperators in a public goods game). The main results of this section will be Theorem 7 and Theorem 8. The former provides explicit formulas for while the latter consists of several upper and lower bounds for . We will need several technically auxiliary lemmas whose proofs will be given in Appendix 1. We start with the following proposition that provides explicit formulas for for .

Proposition 2

The following formulas hold:In particular, if , then . See Appendix 4. The computations of for other k are more involved. We will employ combinatorial techniques and derive recursive formulas for . We defineWe have the following lemma.

Lemma 4

The following recursive relations hold: See Appendix 5. We can decouple the recursive relations in Lemma 4 to obtain recursive relations for and separately as follows:

Lemma 5

The following recursive relations hold See Appendix 6. Using the recursive equations for and we can also derive a recursive relation for .

Proposition 3

satisfies the following recursive relation. See Appendix 7.

Remark 3

Proposition 3 provides a second-order recursive relation for the probabilities . This relation resembles the well-known Chu–Vandermonde identity for binomial coefficients, , which is that, for ,Particularly for we obtainwhere the last identity is Pascal’ rule for binomial coefficients. On the other hand, the recursive formula for becomesUsing the transformation as in the proof of Theorem 7, thenwhich is exactly the Chu–Vandermonde identity for above. Then it is no surprise that in Theorem 7 we obtain that is exactly the same as the binomial coefficient . In the next main theorem we will find explicit formulas for from the recursive formula in the previous lemma using the method of generating functions. The case will be a special one.

Theorem 7

is given explicitly by: for ,For : (i) if k is even, , then(ii) if k is odd, , then See Appendix 8.

Example 3

Below we provide explicit formulas for for :Direct computations verify the recursive formula for We now apply Theorem 7 to the polynomial P in (5) to obtain estimates for , which is the probability that a d-player two-strategy random evolutionary game has m internal equilibria. This theorem extends Theorem 6 for to the general case although we do not achieve an explicit upper bound in terms of d as in Theorem 6.

Theorem 8

The following assertions holdAs consequences: Upper-bound for where can be computed explicitly according to Theorem 7 with n replaced by . Lower-bound for : . Lower-bound for : Upper-bound for : Upper-bound for : For : and . For , . We will apply Decartes’ rule of signs, Proposition 2 and Theorem 7 for the random polynomial (5). It follows from Decartes’ rule of signs thatwhere is given explicitly in Theorem 7 with n replaced by . This proves the first statement. In addition, we can also deduce from Decartes’ rule of signs and Proposition 2 the following estimates for special cases :These computations establish the estimates (ii)–(v) of the theorem. For the consequences: for , in this case the above estimates (ii)–(v) respectively become:which imply that . Similarly for , estimates (ii) and (iii) respectively becomefrom which we deduce that .

Numerical simulations

In this section, we perform several numerical (sampling) simulations and calculations to illustrate the analytical results obtained in previous sections. Figure 1 shows the values of for , for the three cases studied in Theorem 4, i.e., when are i.i.d. standard normally distributed (GD), uniformly distributed (UD1) and when with and being uniformly distributed (UD2). We compare results obtained from analytical formulas in Theorem 4 and from samplings. The figure shows that they are in accordance with each other agreeing to at least 2 digits after the decimal points. Figure 2 compares the new upper bound obtained in Theorem 6 with that of E(d) / m. The comparison indicates which formulas should be used to obtain a stricter upper bound of . Numerical versus simulation calculations of the probability of having a concrete number (m) of internal equilibria, , for different values of d. The payoff entries and were drawn from a normal distribution with variance 1 and mean 0 (GD) and from a standard uniform distribution (UD2). We also study the case where itself is drawn from a standard uniform distribution (UD1). Results are obtained from analytical formulas (Theorem 2) (a) and are based on sampling payoff matrices (b) where payoff entries are drawn from the corresponding distributions. Analytical and simulations results are in accordance with each other. All results are obtained using Mathematica Comparison of the new upper bounds of derived in Theorem 6 with that of E(d) / m: a for the bound in (36) and b for the bound in (37). Black areas indicate when the former ones are better and the grey areas otherwise. Clearly the bound in (a) is stricter/better than that of (b). For small d, the new bounds are better. When d is sufficiently large, we observe that for any d, the new bounds are worse than E(d) / m when m is intermediate while better otherwise. Overall, this comparison indicates which formulas should be used to obtain a stricter upper bound of

Further discussions and future research

In this paper, we have provided closed-form formulas and universal estimates for the probability distribution of the number of internal equilibria in a d-player two-strategy random evolutionary game. We have explored further connections between evolutionary game theory and random polynomial theory as discovered in our previous works (Duong and Han 2015, 2016; Duong et al. 2017). We believe that the results reported in the present work open up a new exciting avenue of research in the study of equilibrium properties of random evolutionary games. We now provide further discussions on these issues and possible directions for future research. Computations of probabilities. Although we have found analytical formulas for it is computationally challenging to deal with them because of their complexity. Obtaining an effective computational method for would be an interesting problem for future investigation. Quantification of errors in the mean-field approximation theory (Schehr and Majumdar 2008). Consider a general polynomial as given in (6) with dependent coefficients, and let be the probability that has m real roots in the interval [a, b] (recall that n is the degree of the polynomial, which is equal to in Equation (1)). The mean-field theory (Schehr and Majumdar 2008) neglects the correlations between the real roots and simply considers that these roots are randomly and independently distributed on the real axis with some local density f(t) at point t, with f(t) being the density that can be computed from the Edelman–Kostlan theorem (Edelman and Kostlan 1995). Within this approximation in the large n limit, the probability is given by a non-homogeneous Poisson distribution, see Schehr and Majumdar (2008, Section 3.2.2 and Equation (70)). By applying the mean-field theory one can approximate the probability that a random d-player two-strategy evolutionary game has m internal equilibria by a simpler and computationally feasible formula. However, it is unclear to us how to quantify the errors of approximation. We leave this topic for future research. Extensions to multi-strategy games. We have focused in this paper on random games with two strategies (with an arbitrary number of players). The analysis of games with more than two strategies is much more intricate since in this case one needs to deal with systems of multi-variate random polynomials. We have provided (Duong and Han 2015, 2016) a closed formula for the expected number of internal equilibria for a multi-player multi-strategy games for the case of normal payoff entries. We aim to extend the present work to the general case in future publications. In particular, Decartes’ rule of signs for multi-variate polynomials (Itenberg and Roy 1996) might be used to obtain universal estimates, regardless of the underlying payoff distribution.
  16 in total

1.  On equilibrium properties of evolutionary multi-player games with random payoff matrices.

Authors:  The Anh Han; Arne Traulsen; Chaitanya S Gokhale
Journal:  Theor Popul Biol       Date:  2012-03-03       Impact factor: 1.570

2.  Equilibrium Points in N-Person Games.

Authors:  J F Nash
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