What compels a system to strive for intelligence and consciousness?
For biology, it is the limited resources, space, and energy (Smith and Morowitz, 2016; Lane, 2015). This scarcity isn’t just a passive constraint—it’s an active selective pressure that shapes behavior at every level, from metabolic pathways to cognitive strategies (West et al., 2007). All biological cells try to be better than their surroundings. Be it a bacteria, fungus, plant, or a cell in an organ inside an animal, a cell in the brain, each cell is doing its best to survive and beat the competition in the environment where it is and ensure it stays relevant. If it does not have the genes to do this, it will get destroyed, and the genes will deteriorate. If none of its species can survive, the genetic instructions for that organism will go extinct, and there will be more space for better-suited alternatives (Dawkins, 1976). This process isn’t just about survival—it’s about optimizing trade-offs between energy expenditure, reproductive success, and environmental adaptation, a principle formalized in life history theory (Stearns, 1992).
This fight for resources is at the core of all the progress we see in the biological world. Combined with random mutations (e.g., from background radiation or replication errors), the world has evolved to contain the whole variety of different insects, animals, plants, mushrooms, and all other organisms (Mayr, 2001). Crucially, these mutations aren’t just random noise—they’re raw material for exaptations, traits that evolve for one purpose but later prove advantageous for another, like feathers evolving for thermoregulation before enabling flight (Gould and Vrba, 1982). In this fight to survive, neural networks have evolved to contain information-processing tools to adapt to changing environments and ensure skills for reproduction, fight, and flight (Kandel et al., 2013). This evolution isn’t linear; it’s a Red Queen’s race — organisms must constantly adapt just to maintain their relative fitness as competitors evolve (Van Valen, 1973).
While these simple automatic responses are what control biological organisms — from simple insects to complex mammals — the skills to adapt vary (Ginsburg and Jablonka, 2019). Simple insects have a very limited capability to adapt to changes in their environment. Worms, for instance, have a basic set of reflexes and instincts but lack the complex neural structures needed for higher-order learning and adaptation (Brenner, 1974). Yet even worms exhibit plasticity — C. elegans can learn to associate smells with food, demonstrating that rudimentary learning emerges wherever there’s selective pressure for flexibility (Ardiel and Rankin, 2010). In contrast, more complex organisms, such as mammals, have developed advanced neural networks capable of not only responding to immediate stimuli but also learning from experiences, solving problems, and even planning for future events (Squire and Kandel, 2009). This shift from reflex to prediction isn’t just quantitative—it’s a phase transition in cognitive complexity, enabled by the evolution of the neocortex and recursive neural circuits (Deacon, 1997). This evolutionary compulsion toward greater intelligence and consciousness is driven by the need for coherence and agency, allowing organisms to navigate their environments more effectively and ensure their survival and reproductive success (Sterelny, 2003; Godfrey-Smith, 2016). But agency comes at a cost: larger brains demand more energy, creating pressure for metabolic efficiency—a trade-off that may explain why intelligence evolves only when ecological niches reward it (Isler and Van Schaik, 2006).
On top of this competition for better and more useful information processing is the human brain. Not only does it have the basic instinctive subconscious drive and automatic responses to obvious threats and opportunities (LeDoux, 1996), but it also has the skills to learn to predict the world around it with extreme accuracy (Clark, 2013). This predictive power isn’t just reactive—it’s generative, allowing humans to simulate counterfactual scenarios and innovate tools, art, and social structures (Corballis, 2011). As it learns to predict the next moment, it does so by learning an approximate abstraction of concepts, such as “falling,” “crashing,” “running,” and “fighting” (Barsalou, 2008). These abstractions aren’t arbitrary; they’re compressed representations of statistically recurrent patterns in the environment, a principle mirrored in machine learning’s latent space (Bengio et al., 2013). This ability to predict the next moment is also at the core of more interesting emergent phenomena, such as music and language (Huron, 2006; Jackendoff, 2002). Language, in particular, may have evolved as a cognitive scaffold—a tool to offload prediction onto social groups, reducing individual computational load (Clark, 2006).
All this competition pushes the realm of biological beings to evolve strategies to co-exist, protect themselves, and still manage to extract resources for their needs (Nowak, 2006). This isn’t just competition—it’s niche construction, where organisms actively modify their environments (and thus selective pressures) in ways that feed back into their own evolution (Odling-Smee et al., 2003). The result is an autonomous system that takes care of itself (Maturana and Varela, 1980). But autonomy has limits: even the most intelligent organisms remain boundedly rational, constrained by cognitive shortcuts and environmental uncertainty (Simon, 1957).
The same dynamics is found in more abstract constructs that human society has built. The stock market for instance exhibits the same Skin in the Game dynamics and seek for a niche. Traders, trading bots and investors find their way of predicting the future and understanding the reality through their useful approximations and abstract concepts in order to gain more resources and stay relevant in the market. Those who fail to adapt, whose predictive models become obsolete, or whose strategies are outmaneuvered by more efficient or insightful competitors, face financial ruin and are purged from the system (Taleb, 2018). This pressure for performance drives a continuous, albeit abstract, evolutionary arms race, where algorithms and human intuition alike are constantly refined, mutated, and selected for their ability to extract value from the market’s inherent uncertainty (Fama, 1970). The market, in essence, becomes a vast, accelerated ecosystem where only the fittest predictive intelligences survive and thrive, constantly pushing the boundaries of information processing and strategic foresight, even as human biases and heuristics introduce systematic deviations from pure rationality (Kahneman and Tversky, 1979).
This parallel between biological evolution and the dynamics of financial markets reveals a deeper truth: intelligence, in its myriad forms, is not merely an emergent property but a tool that emerges from scarcity and competition. Whether it’s a neuron optimizing its firing patterns to predict a predator’s movement, or an algorithm learning to arbitrage micro-fluctuations, the underlying imperative is the same: to process information more effectively, to build more accurate models of reality, and to leverage those models for survival and proliferation. This constant refinement of predictive capacity, driven by the existential threat of irrelevance, is the engine behind all forms of progress, from the simplest cellular adaptation to the most complex human cognition, and indeed, the very striving for consciousness itself.
As we’ve learned from Large Language Models (LLMs), language can be learned by just learning to predict the next word based on the current context (Bengio et al., 2003; Vaswani et al., 2017). This prediction isn’t just statistical—it’s causal inference in disguise, as models implicitly learn syntactic and semantic relationships to minimize surprise (Chomsky, 2017; Lake and Baroni, 2018). This is a highly simplified next step in approximating what humans do. Artificial neural networks are a very simple approximation of what human neurons are (McCulloch and Pitts, 1943), and learning to predict the next word is one of the most simple approximations of what humans do with their neurons, while still giving the network access to all human higher-level knowledge (Devlin et al., 2019). Yet this access is superficial—LLMs lack grounded embodiment, the sensory-motor feedback loops that anchor human concepts in physical experience (Barsalou, 2008; Harnad, 1990).
For digital objects built inside computers, there is a similar “Skin in the Game” dynamic going on. The evolutionary pressure there is not fully enclosed by just this virtual realm of software and algorithms, although evolutionary algorithms are being used to develop software and new algorithms (Holland, 1975; Koza, 1992). Unlike biology, however, digital evolution is Lamarckian—traits acquired during a program’s “lifetime” (e.g., optimized weights in a neural net) can be directly inherited, accelerating adaptation (Whitley, 1994). Instead, the fight for computing resources and energy happens on our smartphones, websites, servers, and PCs. The computational capacity available on Earth is limited (Koomey et al., 2011). This limit isn’t just technical—it’s thermodynamic. The energy costs of training large models are skyrocketing, raising questions about the sustainability of AI scaling laws (Strubell et al., 2019). Servers need to be optimized to take the most out of the resources available. For example, Google has developed advanced algorithms and infrastructure to optimize search queries, reduce latency, and minimize energy consumption (Barroso et al., 2018). This optimization isn’t just about efficiency—it’s about economic survival. In cloud computing, millisecond delays can translate to millions in lost revenue (Dean and Barroso, 2013). Similarly, other tech companies compete to create more efficient software and hardware solutions, ensuring that their digital services run smoothly and cost-effectively. This competition for computational efficiency mirrors the biological struggle for survival, where only the most adaptable and resource-efficient systems thrive (Hill et al., 2013). But unlike biology, digital systems face artificial selection pressures—their fitness is mostly defined by human-designed metrics (e.g., accuracy, speed), not raw survival (Hern, 2021).
In each biological, societal and digital realms, the principle of “Skin in the Game” ensures that systems are incentivized to develop and maintain coherent and effective strategies for survival and success (Taleb, 2018). This coherence isn’t just individual—it’s emergent. In biology, it arises from gene-culture coevolution; in AI, from multi-agent reinforcement learning where competing models shape each other’s development (Leibo et al., 2017). Whether it’s a cell striving to replicate (Alberts et al., 2002), an animal learning to adapt (Shettleworth, 2010), or a digital algorithm seeking to optimize performance (Sutton and Barto, 2018), the imperative for coherence and agency drives progress and innovation. This evolutionary compulsion is the foundation upon which intelligence and consciousness have arisen, and it continues to shape the future of both biological organisms and digital systems.
Skin in the Game, as introduced here, is the qualitative description of the imperative. Chapter 9.5 will give it a quantitative form — the Persistence Ratio \(\mathcal{R} \ge 1\) — and show that what we have so far described as an evolutionary “compulsion” is in fact a strict thermodynamic accounting identity. Every term we have invoked informally in this chapter (energy throughput, predictive accuracy, structural integrity, environmental shielding) will reappear there as a named variable in the Fractal Persistence Equation, and the behavioural consequences for conscious agents will be worked out in Part IV-B.
Where does this strive toward better resource utilization push us? There is currently an intense battle between big AI companies for building better and more capable LLMs (Bommasani et al., 2021). This battle isn’t just technical—it’s geopolitical, with nations racing to dominate AI as a strategic resource (Allen, 2019). As a result of this digital “Skin in the Game,” the LLMs evolve and die out at a rapid pace. There is very limited use of LLM models that were trained two years ago, while billions of users are using the latest models from the past year. The LLMs are forced to evolve—not by themselves (yet), but with the help of developers (Amodei et al., 2016). This dependence raises ethical questions: who controls the evolutionary trajectory of AI? Corporate interests? Open-source communities? Governments? Stock market? (Crawford, 2021).
Computer software themselves does not yet have a similar need to ensure its own survival. Software developers are doing much of the work for them. New versions of software get developed, bugs get fixed, and new features get added once software faces pressure from competition. This dynamic creates a principal-agent problem—developers act as proxies for software “evolution,” but their goals (e.g., profit, user engagement) may misalign with societal well-being (Zuboff, 2019). All this happens without any of our software competing in this race by itself. Recently, with the advent of LLMs, work has been done to enable software development with minimal to no human intervention (Chen et al., 2021), bringing us closer to a future where software might autonomously evolve, adapt, and optimize its own performance, mimicking the evolutionary processes seen in biological systems (Stanley and Miikkulainen, 2002). But autonomy carries risks: uncontrolled recursive self-improvement could lead to misaligned systems, a concern central to AI safety research (Yudkowsky, 2008; Russell, 2019). This trajectory suggests a world where digital entities could increasingly exhibit behaviors and capabilities that blur the line between artificial intelligence and biological intelligence, driven by the same fundamental principles of competition and resource optimization (Russell and Norvig, 2020).
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