The theory of autopoiesis has been influential in many areas of theoretical biology, especially in the fields of artificial life and origins of life. However, it has not managed to productively connect with mainstream biology, partly for theoretical reasons, but arguably mainly because deriving specific working hypotheses has been challenging. The theory has recently undergone significant conceptual development in the enactive approach to life and mind. Hidden complexity in the original conception of autopoiesis has been explicated in the service of other operationalizable concepts related to self-individuation: precariousness, adaptivity, and agency. Here we advance these developments by highlighting the interplay of these concepts with considerations from thermodynamics: reversibility, irreversibility, and path-dependence. We interpret this interplay in terms of the self-optimization model, and present modeling results that illustrate how these minimal conditions enable a system to re-organize itself such that it tends toward coordinated constraint satisfaction at the system level. Although the model is still very abstract, these results point in a direction where the enactive approach could productively connect with cell biology.

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Social insects such as honey bees exhibit complex behavioral patterns, and their distributed behavioral coordination enables decision-making at the colony level. It has, therefore, been proposed that a high-level description of their collective behavior might share commonalities with the dynamics of neural processes in brains. Here, we investigated this proposal by focusing on the possibility that brains are poised at the edge of a critical phase transition and that such a state is enabling increased computational power and adaptability. We applied mathematical tools developed in computational neuroscience to a dataset of bee movement trajectories that were recorded within the hive during the course of many days. We found that certain characteristics of the activity of the bee hive system are consistent with the Ising model when it operates at a critical temperature, and that the system’s behavioral dynamics share features with the human brain in the resting state.

Social insects, such as honey bees exhibit complex behavioral patterns and their inconspicuous coordination enables decision-making on the colony level. It is thus proposed, that a high-level description of their collective behavior might share commonalities with neural processes in the brains. At the same time, recent research concerning overarching features of neural activity implies that brains are poised at the edge of the critical phase transition and that such a state is enabling maximal computational power and adaptability. In our research, we applied some tools developed in the computational neuroscience field to the dataset of bee trajectories recorded within the hive, during the course of many days. Our results imply that certain characteristics of the system are remarkably similar to the Ising model when it operates at critical temperature and also shares some of the features with the human brain at the resting state