Computing Networks:A General Framework to ContrastNeural and Swarm Cognitions

Computing Networks:
A General Framework to Contrast
Neural and Swarm Cognitions

Carlos Gershenson
Computer Sciences Department
Instituto de Investigaciones en Matemáticas Aplicadas y en Sistemas
Universidad Nacional Autónoma de México
Ciudad Universitaria, A.P. 20-726
01000 México D.F. México

This paper presents the Computing Networks (CNs) framework. CNs are used to generalize neural and swarm architectures. Artificial neural networks, ant colony optimization, particle swarm optimization, and realistic biological models are used as examples of instantiations of CNs. The description of these architectures as CNs allows their comparison. Their differences and similarities allow the identification of properties that enable neural and swarm architectures to perform complex computations and exhibit complex cognitive abilities. In this context, the most relevant characteristics of CNs are the existence multiple dynamical and functional scales. The relationship between multiple dynamical and functional scales with adaptation, cognition (of brains and swarms) and computation is discussed.

Keywords: cognition, computation, neural architecture, swarm architecture, swarm cognition, multiple scales.

1 Introduction

The complex behavior exhibited by swarms has been actively studied in recent decades (Hölldobler and Wilson, 1990; Aron et al., 1990; Reznikova, 2007; Ryabko and Reznikova, 2009) and exploited in engineering (Bonabeau et al., 1999; Dorigo and Stützle, 2004; Dorigo et al., 2004). Recent research has highlighted the similarities between swarms and brains, noting that swarms are capable of performing cognitive tasks (Chialvo and Millonas, 1995; Couzin, 2009; Marshall et al., 2009; Passino et al., 2008; Trianni and Tuci, 2009). Contributing to the effort of understanding these similarities, with biological and engineering aims, this paper generalizes models of swarm and neural architectures. In particular, artificial neural networks (ANNs), ant colony optimization (ACO), and particle swarm optimization (PSO) are described under the same general framework. The generalization, named computing networks (CNs), provides a common ground for comparison and for studying the underlying mechanisms and the computational properties common to neural and swarm architectures. As a guiding principle, we can say that neural and swarm architectures compute “unknown” functions , i.e. they explore phase spaces of functions until a satisfactory is found according to certain criteria.

Swarm cognition (Trianni and Tuci, 2009) studies the intersection of the scientific study of natural swarms and neural cognition, with the aim of increasing our understanding of cognition relating it to the self-organization of swarms. CNs provide a general framework to contrast the cognition exhibited by brains and swarms. This particular aim for defining CNs restricts their usefulness, i.e. the purpose of CNs is to increase our understanding of cognitive architectures, not to produce better models or more powerful computational algorithms.

In the next section, the computing networks are defined. In the following sections, CNs are used to describe ANNs, ACO & PSO. These architectures were chosen for their generality and widespread use. More realistic biological models are also presented in terms of CNs within these sections. This is followed by a comparison and discussion. In this section, similarities and differences of the architectures are explored, followed by the discussion multiple dynamical and functional scales. Also, the suitability and equivalence of different architectures is considered. The discussion continues dealing with the cognition of swarm and neural architectures, followed by an examination of alternate descriptions of the architectures. Conclusions close the paper.

2 Computing Networks: A General Descriptive Framework

Many systems can be described as networks, i.e. nodes connected by edges (Newman, 2003; Newman et al., 2006). In this paper, we use the concept of computing network (CN) as a generalization of artificial neural networks (Rumelhart et al., 1986; Hopfield, 1988), ant colony optimization (Dorigo et al., 1991; Dorigo and Stützle, 2004; Dorigo and Blum, 2005; Dorigo, 2007), and particle swarm optimization (Kennedy and Eberhart, 1995, 2001; Dorigo et al., 2008). In this way, the similarities and differences between these characteristic models of neural and swarm intelligence are studied under the same formalism.

A computing network is defined as a set of nodes linked by a set of edges used by an algorithm to compute a function . Nodes and edges can have internal variables that determine their state, and functions that determine how their state changes. This is a very general definition, and can be applied to describe many architectures and models beyond those discussed in this paper. Computing networks can be stochastic or deterministic (depending on the determinism of functions and algorithms), synchronous or asynchronous (depending on the updating used for the change of states of nodes and edges (Gershenson, 2002, 2004b)), discrete (Wuensche, 1998) or continuous (depending on the type of variables of nodes and edges).

3 Artificial Neural Networks

Artificial Neural Networks (ANNs) were originally proposed as logical models of the neocortex (McCulloch and Pitts, 1943). However, their computing power (Hopfield, 1982) has shifted the research focus from their plausibility as neural models to their application in different fields. There are many different types of ANNs, with different properties and implementations (Rumelhart et al., 1986; Kohonen, 2000). Here there will be no focus on any particular type of ANN.

In an ANN instantiation of a CN, nodes are neurons or units. Each neuron typically has a continuous state (output) determined by a function which is composed by two other functions: the weighted sum of its inputs and an activation function such as the hyperbolic tangent. Directed edges (synapses) relate outputs of neurons to inputs of other neurons , as well as external inputs and outputs with the network. Edges have a continuous state (weight) that relates the states of neurons. The function may be given by the states of a subset of (outputs ), or by the complete set . ANNs usually have two dynamical scales: a “fast” scale where the network function is calculated by the functional composition of the function of each neuron , and a “slow” scale where an algorithm adjusts the weights (states) of edges. There is a broad diversity of algorithms used to update weights in different types of ANN. Figure 1 illustrates ANNs as CNs.

Figure 1: Schematic of an ANN instantiation of a CN. Nodes have a function that is computed from its inputs (). Edges have weights to determine the importance of the interaction and also carry the output of neurons and network inputs. The network function or output is given by a subset of node functions . The algorithm changes weights on edges.

4 Ant Colony Optimization

Ant colony optimization (ACO) is a population-based metaheuristic that can be used to find approximate solutions to difficult optimization problems (Dorigo, 2007). ACO is inspired in the collective behavior of ants and their stigmergic interactions through pheromones.

In an ACO instantiation of a CN, nodes are locations that contain a list of “artificial ants” at their location. Each ant has a path which represents a partial solution , from which variables such as distance travelled and nodes visited can be extracted. Edges (trails) have two variables: heuristic value (e.g. distance or cost between two nodes) and pheromone value . There have been different algorithms proposed to calculate function , which is given by the shortest path found. As in ANNs, in ACO there are also two timescales: a “fast” one in which ants travel through the network, generating paths (solutions) by choosing edges probabilistically at each visited node depending on their state ,, and a “slow” one, where the pheromone values of edges are updated. This is similar to weight adjustment in ANNs. The pheromone update consists of an “evaporation” phase, where all levels are reduced (similar to “forgetting” in some ANNs) and an additive phase (similar to “reinforcement” in some ANNs), where pheromone levels associated with good solutions are increased. In some versions of ACO, there is a “middle” scale, where “demon” (problem specific) actions are taken, such as the application of a local search (Dorigo, 2007). Figure 2 illustrates ACO as a CN.

Figure 2: Schematic of an ACO instantiation of a CN. Nodes contain ants that construct paths . Edges contain heuristic and pheromone values. The function is given by the best path found. Algorithm adjusts pheromone concentrations .

It can be argued that ACO—while inspired in the behavior of social insects (Garnier et al., 2007)—does not serve as a realistic biological model. However, CNs can also be used to represent realistic models. Here the models of optimal decision-making presented by Marshall et al. (2009) are discussed. The problem of decision-making can be stated as choosing the best among two or more alternatives. It has been found that cortical neurons and social insects can approach an optimal balance between speed and accuracy in decision-making. Different individuals (neurons, insects, nodes in CNs) explore possibilities and interact (via synapses, pheromones, edges in CNs) to possibly change individual opinions. When a threshold is reached, i.e. enough individuals have made the same choice, the system selects that as a decision. The particularities (function , algorithm ) of each model change, but all of them can be represented in terms of CNs. Here ACO is used as an example, but CNs can be used to compare more realistic models of swarms and brains.

5 Particle Swarm Optimization

Particle swarm optimization (PSO) is a population-based stochastic approach for solving continuous and discrete optimization problems (Dorigo et al., 2008). It was originally inspired by flocking algorithms (Reynolds, 1987) and social psychology research. In PSO, “particles” move in a search space. Their position represents a candidate solution. Particles adjust their position and velocity depending on their neighboring particles in a graph.

In a PSO instantiation of a CN, nodes are particles with position , velocity , value of the best solution found , and a function that the network is trying to optimize. The position represents a tentative solution. The function is simply the best solution found by . Edges represent the relationships between neighboring particles. Typically they contain information about the neighborhood’s best solution, which can be represented as for nodes related by edge . There is a variety of algorithms to relate the way in which particles adjust their state. Again, two timescales can be identified: a “fast” one, where particles evaluate the function they are trying to optimize (), and a “slow” one, where the velocity and position of particles are adjusted by algorithm depending on their previous states and those of their neighbors (links). Figure 3 illustrates PSO as a CN.

For PSO, hypernetworks (Johnson, 2010) can be used as a generalization, so that a single edge can link more than two nodes and to represent the best solution of a neighborhood .

Figure 3: Schematic of an PSO instantiation of a CN. Each node contains the position and velocity of a particle, as well as its best solution found and a function . Edges contain the neighborhood’s best solution . Function is the best solution found by all particles. Algorithm changes the position and velocity of particles depending on the values of their neighbors.

Like with ACO, PSO and other flocking algorithms are inspired in biology (Reynolds, 1987; Rauch et al., 1995), but not quite realistic (Nagy et al., 2010). Nevertheless, CNs can also be used to model realistic models of of flocking. Here we focus on the model of flocking and schooling presented by Couzin et al. (2002). Individuals (birds, fish, nodes) move in space, trying to maintain a minimum distance with their neighbors, i.e. avoid collisions. Also, individuals try to be attracted to their neighbors and align with them. A similar CN instantiation as the one shown in Figure 3 can be used to represent this model, which is considered to be realistic, even when it simplifies local interactions. More complex models (Nagy et al., 2010)—where individuals have different interaction strengths according to their social heirarchy—can also be represented in terms of CNs.

6 Comparison and Discussion

Table 1 shows a comparison of the language used to relate ANNs, ACO, and PSO in terms of CNs. It can be seen that all three architectures have the same basic components: nodes, edges, an algorithm, and a function. However, there are differences in the particularities of each architecture.

Nodes Neurons or units (function ) Nodes (ants (path )) Particles (position , velocity , best solution , function )
Edges Synapses (weight .) Trails (heuristic value , pheromone concentration .) Relationships (neighborhood’s best solution )
Algorithm Adjust edges (.) Adjust edges (.) Adjust nodes (, )
Function Composition of functions of nodes Shortest path () Best solution ()

Table 1: Particular instantiations of CNs: ANN, ACO, and PSO.

ACO and PSO have been used mainly for optimization. This explains why their is the minimum (best) of the solutions found. In contrast, ANNs have been used to solve many different tasks, e.g. classification, generalization, recognition, error correction, and time sequence retention. Still, all of the architectures can be described as computing a function in a distributed fashion. This is because they require the interaction of nodes to produce .

It is interesting to note that, even when ACO and PSO are inspired by swarming systems, algorithms of ANN and ACO are more similar between themselves than with PSO, in the sense that they update edges, while PSO algorithms update nodes. However, the models can be extended from networks to hypernetworks (Johnson, 2010), where there is a duality between nodes and edges, i.e. one can exchange nodes and edges while preserving the functionality of the hypernetwork. In this case, PSO particles can be described as hyperedges, and their interactions as nodes. Then, the PSO algorithm would update hyperedges.

6.1 Dynamical scales

One common characteristic among all three architectures studied is that they have “slow” () and “fast” () dynamical scales. This is no coincidence. Having multiple dynamical scales is a requirement for computing complex functions111A complex function will not be defined formally, but it can be understood as a function that is non-trivially described, explored or optimized. that change in time, i.e. are non-stationary. If there is only change at a single scale, then the phase space of , i.e. all its possible values and potentially its optimum, can be explored, but it cannot be changed. Having two dynamical scales, the changes in the phase space of can be explored as well. This property is essential when is not known beforehand: the algorithm explores different phase spaces until one that satisfies is found.

The tasks solved by real neural and swarm systems also need to exploit the advantages of multiple dynamical scales. In the case of neural systems, learning (synapse modification) enables the correct adjustment of a particular function of a circuit, e.g. categorization. For swarming insects, local interactions (direct or stigmergic) enable the colony to make complex decisions, e.g. choosing a new nest.

Would it be useful to have three dynamical scales? This would imply the exploration of changes in the space of phase spaces of . For example, this is used in “evo-devo” (Fontana, 2002; Munteanu and Solé, 2008) or epigenetic (Balkenius et al., 2001) algorithms, where there is a function , its phase space is explored through the “lifetime” of an “organism” (learning), and the space of possible organisms is explored at an evolutionary scale, e.g. with evolutionary algorithms. An example can be seen with the work of Botee and Bonabeau (1998), where a genetic algorithm is used to find the best parameters of ACO. Figure 4 illustrates the change possible at one, two and three dynamical scales.

Figure 4: Changes at different dynamical scales: (A) single scale: values can vary only along , (B) double scale: apart from changes along , can also be varied, and (C) triple scale: changes in ways in which can be varied can also be explored. Note that these diagrams are only illustrative. can certainly be multidimensional, i.e. in .

It should be noted that multiple dynamical scales are an important feature to enable adaptation (Holland, 1975, 1995). A system can function at a “fast” scale, while adaptation can work at a “slow” scale. When the situation of the system changes, adaptation can change the function of the system to cope with the new situation.

A question that arises is whether CNs with three dynamical scales are computationally equivalent, or more powerful, than CNs with two dynamical scales. The reader is invited to ponder on this question, which is already out of the scope of this paper.

6.2 Functional scales and the relevance of interactions

Apart from having multiple dynamical scales, CNs have multiple functional scales. The most clear scales are those of node (local) and network (global). Subnetworks, modules, layers, or motifs can also form intermediate scales. In CNs, nodes compute certain “local” functions. These functions are combined to produce the CN’s “global” function . However, cannot be reduced to the node functions alone. Since the states of the nodes depend on other nodes, interactions are relevant to determine the future state of nodes, and thus .

As in the case of dynamical scales, having multiple functional scales is a requirement for computing complex functions. In this context, interactions can be described as operators. Local structures (e.g. nodes, motifs) can store certain information and can compute certain functions. However, in many cases, the information produced by local structures is less complex than the one that produced by the global structure (i.e. network). This is because the interactions between local structures integrate information produced at the lower scales to compute the global . The exceptions are trivial, e.g. when all the interactions are weak or absent, or the local structures are redundant. In these cases, one can say that the complexity of the local structures is the same as the complexity of the global one.

This will be clearer introducing a definition of what is meant by complexity: Complexity is the amount of information necessary to describe a phenomenon at a particular scale (Bar-Yam, 2004; Prokopenko et al., 2009; Gershenson, 2007b). With a CN, in most cases more information is necessary to describe the whole network than the collection of all its nodes, namely because of the information contained in edges, which represent interactions. Repeating what was stated above, cannot be reduced to only, namely because of .

A clear example of the relevance of interactions can be seen with cellular automata (CA) (von Neumann, 1966; Wolfram, 1986; Wuensche and Lesser, 1992; Wolfram, 2002), which incidentally can also be described in terms of CNs. The states of cells (nodes) depend on the state of their neighbors (edges) according to a certain rule. In the case of elementary cellular automata (ECA) 110 (Wolfram, 2002; Juárez Martínez et al., 2007), the state at time of each cell depends on its state and of its closest neighbors (3 cells in total) at time . The updating is done synchronously according to the values shown in Table 2. Figure 5 shows the temporal evolution of ECA 110 for a particular initial state. Even when the behavior of ECA 110 is determined by very simple rules, it is capable of universal computation (Cook, 2004), exploiting the interactions between emergent structures (Juárez Martínez et al., 2007) (slow scale) that arise from the simple interactions (fast scale) of the local neighborhoods.

000 0
001 1
010 1
011 1
100 0
101 1
110 1
111 0
Table 2: ECA 110 lookup table. The first column shows the eight possible states of the 3 cells used to update every cell, while the second column shows the state of the updated cell.
Figure 5: Temporal evolution of ECA 110. Each cell is represented by a column and time flows downwards, i.e. each row represents the state of the CA at successive time steps. Black cells represent ’0’ and white cells represent ’1’. The first row (initial state) consists of a single ’1’. The state of other rows depends on the state of the row above. It is not possible to compute a priori the state of the last row from the first row without computing all the intermediate states.

With ECA 110, the relevance of interactions is clearly seen. CNs with simple nodes and functions are capable of complex computations because of the relevant information contained in edges. Note that interactions are not necessarily physical, but they are real. For different systems, there are different “implementations” of edges, e.g. synapses, pheromones, or cues (Couzin, 2009). Still, they all have the same role: to relate states of nodes to compute a distributed function . Using the CN formalism, it can be explained how the computational power of a brain is much more complex than that of a large collection of isolated neurons, and the computational power of a swarm is much more complex than that of a group of isolated insects. Not only interactions are important, but also multiple dynamical and functional scales.

For functional scales, we can also ask whether only two scales are less powerful than more than two scales. However, again, the question is beyond the scope of this paper, although many have discussed the advantages of modularity (Simon, 1996; Schlosser and Wagner, 2004; Callebaut and Rasskin-Gutman, 2005).

6.3 Which architecture is the best?

One might wonder which architecture—ANNs, ACO, or PSO—is the best. There is no best architecture independently of a specific context (Wolpert and Macready, 1995, 1997; Gershenson, 2004a). Different implementations of CNs will be more adequate for different problems, either giving better solutions, or improved speed. The convenience of a particular architecture does not depend only on the problem: different methods will be more useful for different people, depending on their experience and expertise.

A valid question would be: which architecture—ANNs, ACO, or PSO—is more computationally powerful? Since the architectures are so general, it can be conjectured that they are computationally equivalent. For example, one could implement e.g. an ANN based on ACO or PSO, e.g. where the function of a node is itself determined by an ACO or PSO CN. Similarly, one can implement an ACO or PSO based on ANNs. Finally, one can also develop ACO based on PSO and vice versa. It might not be useful at all, but the idea shows that computationally (in Turing’s (1936) sense) they all have similar capacities. A formal proof of this conjecture is beyond the scope of this paper. There will be more differences on particular implementations of ANNs (e.g. given by number of nodes and edges) than between a given ANN and an equivalent ACO or PSO.

The literature is rich in examples of hybrid systems, where some properties of one architecture are combined with those of another one, e.g. (Kennedy and Eberhart, 1995; Wang et al., 2004; Chen et al., 2004; Blum and Socha, 2005; Mozafari et al., 2006; Martin and Reggia, 2010) to cite a few of them. Actually, the original PSO paper (Kennedy and Eberhart, 1995) used PSO as an example to train an ANN. This illustrates that for a particular problem and for a particular expertise of the developers, no single approach gives the best solutions.

Having discussed the similarity of the computational capacities of neural and swarm architectures, we can continue with the discussion about the role of the architectures in cognition.

6.4 Cognition

Cognition comes from the Latin cognoscere, which means “get to know”. We can say that a system is cognitive if it knows something (Gershenson, 2004a). With this definition, it is not possible to draw a boundary between cognitive and non-cognitive systems. Since somebody has to judge whether a system knows or not, it is partly observer-dependent. Instead of discussing whether a system is cognitive or not, it is more fruitful to distinguish different types of cognition (e.g. human, animal, biological (including plant and bacterial), social, artificial, adaptive, systemic (Gershenson, 2004a)), to compare and better understand them.

From this perspective, it is clear that swarms are cognitive systems because they know how to forage, find sites, build nests, and even add and subtract small numbers (Reznikova, 2007; Ryabko and Reznikova, 2009). Neural architectures are cognitive because they know how to categorize, classify, remember, etc. (Hopfield, 1982). To compare both types of cognition, we can use the concept of computing networks proposed in this paper.

Cognition can be seen as the ability to compute a function . This is because if a system can compute , we can say that it knows how to calculate . This vocabulary does not aim at ascribing to CNs a “mind”, “consciousness”, or other difficult-to-define property usually associated with human cognition. The aim of this use of language is to be able to compare the cognitive capacities of neural and swarm architectures. As discussed in the previous subsection, neural and swarm architectures have similar computational abilities, shown by their generalization as CNs. If we describe cognition as computation, it naturally follows that neural and swarm architectures have similar cognitive capacities, in theory. In practice, different implementations will have different cognitive abilities, just as a human brain has different abilities as a rat brain: the former is potentially better at poetry, the latter is potentially better at navigation. Also, differences of timescale are important, i.e. brains usually compute at faster timescales than swarms.

The great advantage of swarm and neural cognition is that they manage to exploit the benefits of multiple functional and dynamical scales to exhibit complex cognitive abilities. As discussed above, multiple scales enable CNs to compute more complex functions and to adapt to changes in the environment. In cognitive terms, the structure represented by CNs enables neural and swarm architectures to exhibit a more complex cognition, as compared to a system with a single functional or dynamical scale, e.g. a thermostat. We can see that there are cognitive systems with more than two scales, e.g. group cognition (Stahl, 2006), which exploit and combine the cognitive abilities of a collection of humans. Naturally, swarms are another example of multiple scale cognition, since the cognition of individual insects is provided by a neural architecture.

6.5 Alternative descriptions

The description of ANN, ACO, and PSO in terms of computing networks is only one of several possible languages that can be used to compare the architectures. For example, a multi-agent description can be also used: Nodes can be described as agents and edges can be described as interactions. An algorithm regulates the interactions between agents to reach a global state (equivalent to function ). This global state can be described as being reached by self-organization (Gershenson and Heylighen, 2003). This self-organization in a multi-agent system is comparable to the distributed computation of . The system can compute the same function , only the description changes. For the purposes pursued in this paper, the network description seems more appropriate. A multi-agent description can be valuable in the process of designing algorithms, since goals of agents and systems can be defined. Then, the algorithm should minimize “friction” (i.e. negative interactions) and promote “synergy” (positive interactions) (Gershenson, 2007a). This will necessarily increase the system’s “satisfaction”, which is basically what we want the system to do, i.e. .

Yet another description that can be used is that of information (Gershenson, 2007b). Nodes, edges, algorithms, and functions can be all seen as information, while computation can be seen as a change of information. This is a more general description, so it is not so useful for making a comparison as the one presented here. The information framework might be useful for finding general principles across disciplines, since everything can be described in terms of information.

Neural and swarm architectures can also be described in terms of differential equations, dynamical systems theory, object-oriented programming, rules, zeros and ones, etc. Different descriptions are suitable for different contexts and purposes (Gershenson, 2004a). The purpose of computing networks is specifically the comparison of neural and swarm architectures. CNs will not be as good as the original descriptions for developing e.g. new learning algorithms in ANNs or new optimization algorithms in ACO. This is because the computing networks description is more general and vague than an actual instantiation of an ANN or PSO. More details are required at the implementation level, which were neglected here. The goal of defining CNs is more theoretical than practical: to understand the similarities and differences of neural and swarm architectures, not to improve current technical algorithms. CNs are not better or worse that other descriptions. Here they were useful to understand the relevance of multiple scales and some computational principles common to neural and swarm architectures at a general level. It might have been made with a different description, but CNs seemed the most appropriate for the purposes of this work.

7 Conclusions

As Trianni and Tuci suggest (Trianni and Tuci, 2009), the principles of swarms can be useful tools for studying the neuroscientific basis of cognition. Here it was shown that both swarm and neural architectures share similar computational and cognitive abilities. This was achieved by defining computing networks (CNs), which are able to generalize neural and swarm architectures, allowing their comparison. CNs can also be useful to generalize and compare other swarm intelligence algorithms, e.g. (Pham et al., 2006; Yang, 2009; Krishnanand and Ghose, 2009). By studying the general principles that enable CNs to perform complex computations, one can understand better what are the requirements of neural and swarm systems to exhibit complex cognition. In this paper, the importance of having multiple dynamical and functional scales to exhibit complex cognition and adaptation was discussed. From a cognitive perspective, CNs support the thesis of neural and swarm architectures having similar cognitive abilities. CNs also show that neural and swarm architecture have similar computational abilities.


I should like to thank Dante Chialvo, Vito Trianni, Elio Tuci, Tamás Vicsek, and anonymous referees for useful comments. This work was partially supported by SNI membership 47907 of CONACyT, Mexico.


  • Aron et al. (1990) Aron, S., Deneubourg, J. L., Goss, S., and Pasteels, J. M. (1990). Functional self-organization illustrated by inter-nest traffic in ants: The case of the argentinian ant. In Biological Motion, W. Alt and G. Hoffman, (Eds.). Lecture Notes in BioMathematics, vol. 89. Springer, Berlin, 533–547. URL
  • Balkenius et al. (2001) Balkenius, C., Zlatev, J., Brezeal, C., Dautenhahn, K., and Kozima, H., Eds. (2001). Proceedings of the First International Workshop on Epigenetic Robotics: Modeling Cognitive Development in Robotic Systems. Vol. 85. Lund University Cognitive Studies, Lund, Sweden. URL
  • Bar-Yam (2004) Bar-Yam, Y. (2004). Multiscale variety in complex systems. Complexity 9 (4): 37–45. URL
  • Blum and Socha (2005) Blum, C. and Socha, K. (2005). Training feed-forward neural networks with ant colony optimization: An application to pattern classification. Hybrid Intelligent Systems, International Conference on: 233–238. URL
  • Bonabeau et al. (1999) Bonabeau, E., Dorigo, M., and Theraulaz, G. (1999). Swarm Intelligence: From Natural to Artificial Systems. Santa Fe Institute Studies in the Sciences of Complexity. Oxford University Press, New York.
  • Botee and Bonabeau (1998) Botee, H. M. and Bonabeau, E. (1998). Evolving ant colony optimization. Advances in Complex Systems 1: 149–159.
  • Callebaut and Rasskin-Gutman (2005) Callebaut, W. and Rasskin-Gutman, D. (2005). Modularity: Understanding the Development and Evolution of Natural Complex Systems. MIT Press.
  • Chen et al. (2004) Chen, Y., Yang, B., and Dong, J. (2004). Evolving flexible neural networks using ant programming and pso algorithm. Advances in Neural Networks –ISNN 2004: 211–216. URL
  • Chialvo and Millonas (1995) Chialvo, D. and Millonas, M. (1995). How swarms build cognitive maps. In The biology and technology of intelligent autonomous agents, L. Steels, (Ed.). Vol. 144. 439–450. URL
  • Cook (2004) Cook, M. (2004). Universality in elementary cellular automata. Complex Systems 15 (1): 1–40.
  • Couzin (2009) Couzin, I. D. (2009). Collective cognition in animal groups. Trends in Cognitive Sciences 13 (1): 36 – 43. URL
  • Couzin et al. (2002) Couzin, I. D., Krause, J., James, R., Ruxton, G. D., and Franks, N. R. (2002). Collective memory and spatial sorting in animal groups. Journal of Theoretical Biology 218 (1): 1–11. URL
  • Dorigo (2007) Dorigo, M. (2007). Ant colony optimization. Scholarpedia 2 (3): 1461. URL
  • Dorigo and Blum (2005) Dorigo, M. and Blum, C. (2005). Ant colony optimization theory: A survey. Theoretical Computer Science 44 (2-3): 243–278. URL
  • Dorigo et al. (1991) Dorigo, M., Maniezzo, V., and Colorni, A. (1991). Positive feedback as a search strategy. Tech. Rep. 91-016, Dipartimento di Elettronica, Politecnico di Milano.
  • Dorigo et al. (2008) Dorigo, M., Montes de Oca, M. A., and Engelbrecht, A. (2008). Particle swarm optimization. Scholarpedia 3 (11): 1486. URL
  • Dorigo and Stützle (2004) Dorigo, M. and Stützle, T. (2004). Ant Colony Optimization. MIT Press.
  • Dorigo et al. (2004) Dorigo, M., Trianni, V., Şahin, E., Groß, R., Labella, T. H., Baldassarre, G., Nolfi, S., Deneubourg, J.-L., Mondada, F., Floreano, D., and Gambardella, L. (2004). Evolving self-organizing behaviors for a swarm-bot. Autonomous Robots 17 (2-3): 223–245. URL
  • Fontana (2002) Fontana, W. (2002). Modelling ’evo-devo’ with RNA. BioEssays 24 (12): 1164–1177. URL
  • Garnier et al. (2007) Garnier, S., Gautrais, J., and Theraulaz, G. (2007). The biological principles of swarm intelligence. Swarm Intelligence 1 (1): 3–31. URL
  • Gershenson (2002) Gershenson, C. (2002). Classification of random Boolean networks. In Artificial Life VIII: Proceedings of the Eight International Conference on Artificial Life, R. K. Standish, M. A. Bedau, and H. A. Abbass, (Eds.). MIT Press, pp. 1–8. URL
  • Gershenson (2004a) Gershenson, C. (2004a). Cognitive paradigms: Which one is the best? Cognitive Systems Research 5 (2) (June): 135–156. URL
  • Gershenson (2004b) Gershenson, C. (2004b). Updating schemes in random Boolean networks: Do they really matter? In Artificial Life IX Proceedings of the Ninth International Conference on the Simulation and Synthesis of Living Systems, J. Pollack, M. Bedau, P. Husbands, T. Ikegami, and R. A. Watson, (Eds.). MIT Press, pp. 238–243. URL
  • Gershenson (2007a) Gershenson, C. (2007a). Design and Control of Self-organizing Systems. CopIt Arxives, Mexico. URL
  • Gershenson (2007b) Gershenson, C. (2007b). The world as evolving information. In Proceedings of International Conference on Complex Systems ICCS2007, Y. Bar-Yam, (Ed.). URL
  • Gershenson and Heylighen (2003) Gershenson, C. and Heylighen, F. (2003). When can we call a system self-organizing? In Advances in Artificial Life, 7th European Conference, ECAL 2003 LNAI 2801, W. Banzhaf, T. Christaller, P. Dittrich, J. T. Kim, and J. Ziegler, (Eds.). Springer, Berlin, pp. 606–614. URL
  • Holland (1975) Holland, J. H. (1975). Adaptation in natural and artificial systems. The University of Michigan Press.
  • Holland (1995) Holland, J. H. (1995). Hidden Order: How Adaptation Builds Complexity. Helix books. Addison-Wesley.
  • Hölldobler and Wilson (1990) Hölldobler, B. and Wilson, E. O. (1990). The Ants. Belknap Press.
  • Hopfield (1982) Hopfield, J. (1982). Neural networks and physical systems with emergent collective computational abilities. Proceedings of the National Academy of Sciences 79 (8): 2554. URL
  • Hopfield (1988) Hopfield, J. (1988). Artificial neural networks. Circuits and Devices Magazine, IEEE 4 (5) (Sep): 3–10. URL
  • Johnson (2010) Johnson, J. (2010). Hypernetworks in the Science of Complex Systems. Series on Complexity Science, vol. 1. World Scientific. URL
  • Juárez Martínez et al. (2007) Juárez Martínez, G., McIntosh, H. V., Seck Tuoh Mora, J. C., and Chapa Vergara, S. V. (2007). Rule 110 objects and other collision-based constructions. Journal of Cellular Automata 2 (3): 219–242.
  • Kennedy and Eberhart (1995) Kennedy, J. and Eberhart, R. (1995). Particle swarm optimization. In Proceedings of IEEE International Conference on Neural Networks. IEEE Press, Piscataway, NJ, pp. 1942–1948. URL
  • Kennedy and Eberhart (2001) Kennedy, J. and Eberhart, R. (2001). Swarm Intelligence. Morgan Kaufmann, San Francisco, CA.
  • Kohonen (2000) Kohonen, T. (2000). Self-Organizing Maps, 3rd ed. Springer.
  • Krishnanand and Ghose (2009) Krishnanand, K. N. and Ghose, D. (2009). Glowworm swarm optimization for simultaneous capture of multiple local optima of multimodal functions. Swarm Intelligence 3 (2) (June): 87–124. URL
  • Marshall et al. (2009) Marshall, J. A., Bogacz, R., Dornhaus, A., Planqué, R., Kovacs, T., and Franks, N. R. (2009). On optimal decision-making in brains and social insect colonies. Journal of the Royal Society Interface. URL
  • Martin and Reggia (2010) Martin, C. and Reggia, J. (2010). Self-assembly of neural networks viewed as swarm intelligence. Swarm Intelligence 4 (1) (03): 1–36. URL
  • McCulloch and Pitts (1943) McCulloch, W. and Pitts, W. (1943). A logical calculus of the ideas immanent in nervous activity. Bulletin of Mathematical Biology 5 (4): 115–133. URL
  • Mozafari et al. (2006) Mozafari, B., Ranjbar, A. M., Amraee, T., Mirjafari, M., and Shirani, A. R. (2006). A hybrid of particle swarm and ant colony optimization algorithms for reactive power market simulation. Journal of Intelligent and Fuzzy Systems 17 (6) (January): 557–574. URL
  • Munteanu and Solé (2008) Munteanu, A. and Solé, R. V. (2008). Neutrality and robustness in evo-devo: Emergence of lateral inhibition. PLoS Comput Biol 4 (11) (11): e1000226. URL
  • Nagy et al. (2010) Nagy, M., Ákos, Z., Biro, D., and Vicsek, T. (2010). Hierarchical group dynamics in pigeon flocks. Nature 464: 890–893. URL
  • Newman et al. (2006) Newman, M., Barabási, A.-L., and Watts, D. J., Eds. (2006). The Structure and Dynamics of Networks. Princeton Studies in Complexity. Princeton University Press.
  • Newman (2003) Newman, M. E. J. (2003). The structure and function of complex networks. SIAM Review 45: 167–256. URL
  • Passino et al. (2008) Passino, K. M., Seeley, T. D., and Visscher, P. K. (2008). Swarm cognition in honey bees. Behavioral Ecology and Sociobiology 62 (3) (January): 401–414. URL
  • Pham et al. (2006) Pham, D., Ghanbarzadeh, A., Koc, E., Otri, S., Rahim, S., and Zaidi, M. (2006). The bees algorithm–a novel tool for complex optimisation problems. In Intelligent production machines and systems: 2nd I* PROMS Virtual Conference, 3-14 July 2006. Elsevier Science, p. 454. URL
  • Prokopenko et al. (2009) Prokopenko, M., Boschetti, F., and Ryan, A. (2009). An information-theoretic primer on complexity, self-organisation and emergence. Complexity 15 (1): 11 – 28. URL
  • Rauch et al. (1995) Rauch, E. M., Millonas, M. M., and Chialvo, D. R. (1995). Pattern formation and functionality in swarm models. Physics Letters A 207 (3–4): 185–193. URL
  • Reynolds (1987) Reynolds, C. W. (1987). Flocks, herds, and schools: A distributed behavioral model. Computer Graphics 21 (4): 25–34. URL
  • Reznikova (2007) Reznikova, Z. (2007). Animal Intelligence From Individual to Social Cognition. Cambridge University Press.
  • Rumelhart et al. (1986) Rumelhart, D. E., McClelland, J. L., and the PDP Research Group, Eds. (1986). Parallel Distributed Processing: Explorations in the Microstructure of Cognition. MIT Press.
  • Ryabko and Reznikova (2009) Ryabko, B. and Reznikova, Z. (2009). The use of ideas of information theory for studying “language” and intelligence in ants. Entropy 11 (4): 836–853. URL
  • Schlosser and Wagner (2004) Schlosser, G. and Wagner, G. P. (2004). Modularity in Development and Evolution. The University of Chicago Press.
  • Simon (1996) Simon, H. A. (1996). The Sciences of the Artificial, 3rd ed. MIT Press.
  • Stahl (2006) Stahl, G. (2006). Group Cognition: Computer Support for Building Collaborative Knowledge. MIT Press.
  • Trianni and Tuci (2009) Trianni, V. and Tuci, E. (2009). Swarm cognition and artificial life. In Advances in Artificial Life. Proceedings of the 10th European Conference on Artificial Life (ECAL 2009).
  • Turing (1936) Turing, A. M. (1936). On computable numbers, with an application to the Entscheidungsproblem. Proceedings of the London Mathematical Society, Series 2 42: 230–265. URL
  • von Neumann (1966) von Neumann, J. (1966). The Theory of Self-Reproducing Automata. University of Illinois Press. Edited by A. W. Burks.
  • Wang et al. (2004) Wang, Z., Durst, G. L., Eberhart, R. C., Boyd, D. B., and Miled, Z. B. (2004). Particle swarm optimization and neural network application for qsar. In In HiCOMB. pp. 26–30.
  • Wolfram (1986) Wolfram, S. (1986). Theory and Application of Cellular Automata. World Scientific.
  • Wolfram (2002) Wolfram, S. (2002). A New Kind of Science. Wolfram Media. URL
  • Wolpert and Macready (1997) Wolpert, D. and Macready, W. (1997). No Free Lunch Theorems for Optimization. IEEE Transactions on Evolutionary Computation 1 (1): 67–82.
  • Wolpert and Macready (1995) Wolpert, D. H. and Macready, W. G. (1995). No free lunch theorems for search. Tech. Rep. SFI-WP-95-02-010, Santa Fe Institute. URL
  • Wuensche (1998) Wuensche, A. (1998). Discrete dynamical networks and their attractor basins. In Complex Systems ’98, R. Standish, B. Henry, S. Watt, R. Marks, R. Stocker, D. Green, S. Keen, and T. Bossomaier, (Eds.). University of New South Wales, Sydney, Australia, pp. 3–21. URL
  • Wuensche and Lesser (1992) Wuensche, A. and Lesser, M. (1992). The Global Dynamics of Cellular Automata; An Atlas of Basin of Attraction Fields of One-Dimensional Cellular Automata. Santa Fe Institute Studies in the Sciences of Complexity. Addison-Wesley, Reading, MA.
  • Yang (2009) Yang, X.-S. (2009). Firefly algorithms for multimodal optimization. In SAGA (2009-10-06), O. Watanabe and T. Zeugmann, (Eds.). Lecture Notes in Computer Science, vol. 5792. Springer, pp. 169–178. URL
Comments 0
Request Comment
You are adding the first comment!
How to quickly get a good reply:
  • Give credit where it’s due by listing out the positive aspects of a paper before getting into which changes should be made.
  • Be specific in your critique, and provide supporting evidence with appropriate references to substantiate general statements.
  • Your comment should inspire ideas to flow and help the author improves the paper.

The better we are at sharing our knowledge with each other, the faster we move forward.
The feedback must be of minimum 40 characters and the title a minimum of 5 characters
Add comment
Loading ...
This is a comment super asjknd jkasnjk adsnkj
The feedback must be of minumum 40 characters
The feedback must be of minumum 40 characters

You are asking your first question!
How to quickly get a good answer:
  • Keep your question short and to the point
  • Check for grammar or spelling errors.
  • Phrase it like a question
Test description