The de facto goal of science, for most of its practitioners, has become not simply to explain our world, but to account for it completely in terms of physical processes. Before the scientific revolution, God, spirits and other kinds of non-material forces were evoked as explanations of natural phenomena. Even after the scientific method became established, and physical processes or mechanisms became provided for an increasing number of natural phenomena, an appeal to other explanations, often by scientists themselves, continued. It was not until this century that vitalism—the notion that living things are animated by a force not present in matter—was universally abandoned. And even today, some philosophers question whether science will ever be able to account for consciousness completely in material terms.
In other words, science from its beginning has been engaged in a relentless battle against all forms of dualism, the notion that there is ultimately anything other than material processes. Terrence Deacon is a scientist who is completely onboard with this program, but he thinks that science has been going about it in the wrong way. He argues that life and mind manifest a number of properties that, while originating from ordinary physical processes in a potentially explainable fashion, are nevertheless not material in the usual way that we think of that term, and need to be acknowledged as such.
He calls these properties absential, because they can’t be located in any purely physical process. We constantly acknowledge their existence; they include such features as function, purpose, goal, value, meaning and reference. Yet they seem to defy explanation in physical terms. Thus science tends to ignore them, implicitly or explicitly:
absential features must, by definition, be treated as epiphenomenal glosses that need to be reduced to specific physical substrates or else excluded from the analysis. The realm that includes what is merely represented, what-might-be, what-could-have-been, what-it-feels-like, or is-good-for, presumably can be of no physical relevance. (p. 5)
What makes ententional processes so cryptic is that they exhibit properties that appear merely superimposed on materials or physical events, as though they are something in addition to and separate from their material-physical embodiment. (pp. 56-7)
Chief among these absential properties is a phenomenon, or set of phenomena, he calls ententionality. It is closely related to intentionality, the human attribute of being oriented towards some goal or purpose, but Deacon coins it with the aim of a broader meaning that allows it to be extended to much simpler forms of life:
Ententional phenomena include functions that have satisfaction conditions, adaptations that have environmental correlates, thoughts that have contents, purposes that have goals, subjective experiences that have a self/other perspective, and values that have a self that is benefited or harmed. (p. 27)
For example, Deacon would say that a bacterial cell exhibits ententional behavior, because it functions to maintain itself. It is not simply a complex association of millions of molecules and macromolecules, organized in a very specific fashion, but behaves in a way to perpetuate this organization. It takes in substances that can be transformed into critical cell components, and resists environmental conditions that would threaten its integrity. All of its behavior is directed towards the preservation of this complex structure.
While this kind of behavior “is not a purpose in any usual sense,” Deacon acknowledges,
neither is it a chemical-mechanical relationship. Though subjective awareness is different from the simple functional responsiveness of organisms in general, both life and mind have crossed a threshold to a realm where more than just what is materially present matters. (p. 26)
The notion of purpose, however, has long been anathema to science. The great significance and success of Darwinism is that it is able to explain the appearance of new living forms, well adapted to their environment, as the outcome of processes with no goal or purpose whatsoever. While we commonly speak of living things and their processes as exhibiting purposeful behavior—when we say the function of the digestive tract is to begin the transformation of nutrients, or the function of the lungs is to take in oxygen, or a function of the brain is to think—this is generally understood as just a useful way of describing what happens. The organs behave “as if” they had a purpose. Yet the physical processes that compose them can apparently have none.
The problem with this standard scientific view, Deacon points out, is that goals, purposes, and other absential features do in fact exist, in some sense, at least for our species, and play a crucial role in our lives. We all have goals and purposes. We value some things more than others, distinguish good from bad, use symbols to refer to things, find meaning in life. Moreover, these absential features, whatever their relationship to the physical world, seem to interact with it. Thus we say that we act in certain ways because we are motivated by some goal or purpose, because of the way some situation seems to be, by something that isn’t but could be. Though somewhat controversial, most philosophers believe that notions like these are a cause of our behavior.
So where do absential features come from? If we are to reject a dualistic explanation, they must have evolved, and In Incomplete Nature, Deacon sets himself the task of showing how this happened. He argues that to understand this, we need to think not in positive terms—what is added to physical processes—but in negative terms, what is taken away from them. Specifically, he believes we should focus on constraints, barriers that limit the natural flow of physical processes, and thus have the potential to channel them in certain directions.
To take an extremely simple example, a whirlpool in a stream is formed as a result of some object that obstructs the natural flow of the water. It defies precise description in purely physical terms, because the individual water molecules that compose it are constantly moving about and shifting. There is no single configuration of them that we can point to and say, this is a whirlpool. We might define the whirlpool as a certain pattern of water molecules, but pattern, Deacon cautions us, is not an objective term. What is perceived as a pattern depends to some extent on the observer. This will not do for a scientific explanation.
Deacon argues that the most appropriate way to define a whirlpool is in terms of constraint. The obstacle in the path of the stream prevents the water from moving in certain directions that it otherwise would move in. Just how much the water is constrained—what directions it could move in, but is prevented from moving in by the object—can be precisely and objectively defined:
Constraints are what is not there but could have been, irrespective of whether this is registered by any act of observation. (p. 192)
order is commonly defined relative to the expectations and aesthetics of an observer. In contrast, constraint can be objectively and unambiguously assessed. (p. 195)
Thus to Deacon, “evolution is not imposed design, but progressive restraint.” (pp. 425-6). What has enabled more complex organisms to evolve is their ability to create successively more constraints on physical processes. The meat of the book is devoted to explaining in some detail how this occurs.
Order without Purpose
According to Deacon, there are two distinct stages that are essential in making the transition from non-living processes—what physical scientists would call thermodynamic phenomena–to the ententional features associated with living, intelligent organisms. The first step creates what he calls morphodynamic systems. The prefix morpho- refers to the fact that these systems take on a particular large-scale (relative to the size of individual molecules) geometry or shape; this shape can then have physical consequences quite independently of the underlying thermodynamics. Specifically, he defines morphodynamic systems by “the[ir] tendency to become spontaneously more organized and orderly over time due to constant perturbation.” (p. 237). He provides several examples of them.
I mentioned the whirlpool earlier, in which water molecules in a stream become organized in response to a perturbation of the naturally-flowing water. A slightly more complex example is provided by convection cells. When an open container containing a very thin layer of water is heated from below, the heat gradually spreads throughout the entire container, and is lost or dissipated from the system through radiation and vaporization into the air. If the intensity of heat is relatively low, this process occurs through purely thermodynamic processes. Individual water molecules, absorbing the heat energy, move faster, and collide with cooler, slower molecules above them, transferring some of the heat to them.
However, this is a relatively slow process, and if the source of heat is intense enough, this intensity in effect overwhelms the capacity of these individual molecular movements to dissipate the heat fast enough. In this case, the water molecules may organize in a fashion that allows faster heat dissipation. Instead of moving individually, large number of heated molecules coalesce in a group, and carry the heat upwards in ordered columns. The columns have a hexagonal cross-section because this maximizes packing, that is, the number of columns that can be formed in a given cross-section of water. These columns are maintained as long as heat continues to be applied to the water.
The key factor, then, is the constant perturbation of the water caused by the heat. Basic physical laws dictate that the system will attempt to dissipate this perturbing energy, so no physical laws are transgressed by the system. Yet with a strong enough perturbation, the system will organize in a way that seems to run counter to the flow of normal thermodynamic properties. Something new has appeared.
At this point, Deacon makes a distinction between what he calls orthograde and contragrade changes:
I will call changes in the state of a system that are consistent with the spontaneous, “natural” tendency to change, irrespective of external interference, orthograde changes. The term literally refers to going with the grade or tilt or tendency of things, as in falling, or “going with the flow.” In contrast, I will call changes in the state of a system that must be extrinsically forced, because they run counter to orthograde tendencies, contragrade changes. (p. 223)
The movement of individual water molecules in response to heat is an orthograde process; it is standard thermodynamics. However, the imposition of an external heat source creates a contragrade process. It results in a concentrated, or uneven, distribution of heat in the water, which in effect opposes the natural thermodynamic tendency for heat to be uniformly distributed. This latter tendency constrains the water molecules, opposing their orthograde tendency to move in a way that dissipates heat. The two forces, working together, are what creates the convection cells.
Deacon argues that all morphodynamic systems, as well as more complex forms of order, result from such a clash of forces:
Because the world is structured and not uniform, and because there are many distinct dimensions of orthograde change possible (involving different properties of things, such as temperature, mass, movement, charge, structural form, etc.), certain of these tendencies can interact in relative isolation from others. Contragrade change is the natural consequence of one orthograde process influencing a different orthograde process—for example, via some intervening medium. This implies that in one sense all change ultimately originates from spontaneous processes. It is simply because the world is highly heterogeneous that there can be contragrade processes. (p. 224)
The orthograde/contragrade distinction is somewhat relative. What is contragrade at one level may be orthograde at another. For example, when individual atoms collide with each other, their paths in space are altered. This can be considered a contragrade change at the level of these atoms. But at the level of thermodynamics, which involves the collective actions of enormous numbers of atoms, these contragrade changes are part of an orthograde process, as when a gas diffuses to fill a space.
The Emergence of Self
Morphodynamic systems are therefore capable of using certain constraints to create order, but is this the key to life? Deacon thinks an additional step is necessary. Morphodynamic systems, as I just emphasized, are dependent on some kind of continuous perturbation coming from outside of them. Convection cells must be sustained by constant heat of a certain intensity. If the heat lessens or stops, the order is disrupted. Likewise, the whirlpool’s existence depends on some obstacle outside of it that blocks or diverts the flow of water. The same general principle is at work for other examples of morphodynamic systems that he discusses, which involve light or movement of air in particular ways.
It’s clear that living things could not survive long if they remained so dependent on such chance conditions. In order to maintain morphodynamic organization against fluctuations in the environment, they need to be able to insure a constant input of energy and materials—in other words, to create their own constraints. A system that can do this Deacon refers to as teleodynamic. It “is organized with respect to its own persistence.” (p. 270). Now it is legitimate to say that its
processes are functions, not merely chemical reactions, because they exist to produce specific self-promoting physical consequences..[they] exist for the sake of preserving the integrity and persistence of these integrated systems (p. 273).
To illustrate this, Deacon discusses a prototype teleodynamic system, which he refers to as an autogen (“self-creating”). It is composed of two morphodynamic systems that couple together in a synergistic fashion. The first system is an autocatalytic set, a series of linked metabolic reactions in which one substance or substrate is progressively transformed into other substances (just as occurs, in much more complex fashion, in all living cells today). For any single metabolic reaction to occur at a significant rate, it is generally necessary for a catalyst to be present, another substance that binds to the substrate in a way that enhances the molecular rearrangements involved in its transformation. In all living cells, catalysis is performed by specialized protein molecules, or enzymes.
In the very primitive conditions in which life was first developing, there would have been no enzymes. However, other, simpler organic molecules may to some extent act as catalysts. Moreover, as has been shown by other researchers, particularly Stuart Kauffman, if enough metabolic reactions occur in close proximity, the odds are favorable that each reaction can be catalyzed to a significant extent by a substance that is produced by one of the other reactions. In other words, if there is a pool of many different substances, each one will have some ability to catalyze a reaction needed to form another. In this situation, the entire set of reactions is synergistic, and may proceed until the most basic substances, those needed to input into the network and begin the transformation, are exhausted. In this sense, Deacon says, “autocatalysis is thus self-promoting, but not self-regulating or self-preserving.” (p. 295).
The second morphodynamic system Deacon refers to as containment. In his autogen model, this is created by a certain kind of molecule that can polymerize, or join together with other like molecules, to form a large planar or sheet-like structure of repeating units. One might visualize this as a jigsaw puzzle that is formed by identically-shaped pieces that can fit into each other. If this structure becomes large enough, it may fold back on itself into a spherical form. It then has the possibility of enclosing the autocatalytic set, isolating it from the surrounding medium, somewhat as membranes enclose all living cells today.
At this point, according to Deacon, each morphodynamic system can potentially synergize with or complement the other. The containment structure, by enclosing the autocatalytic loop in a relatively small space, can in effect corral the reacting substances, preventing them from diffusing away from each other. The resulting increase in their concentration thus accelerates the individual reactions, and enhances the probability that a substance created by one will be accessible as a catalyst for another. In addition, the containment structure provides a protective barrier that reduces the possibility of autocatalysis being disrupted by inappropriate substances. Deacon speculates that when the autocatalytic network exhausts the supply of substances that it requires, the containment may allow it to enter a sort of latent or hibernating state, to be activated again when a fresh supply of substances is encountered.
Conversely, the autocatalytic loop, if it happens to produce the kind of molecule able to polymerize, can promote the formation of the containment structure by constantly supplying more of this substance. Thus each morphodynamic process enhances the other, and in Deacon’s view, produces a system for which the word “self” becomes appropriate:
the reciprocal complementarity of these two self-organizing processes creates the potential for self-repair, self-reconstitution, and even self-replication in a minimal form. (p. 305)
In other words, while this autogen is a very simple system, still falling far short of a living cell, it has the potential to evolve further. Once the basis for self sustainment has been put into place, it is not difficult to imagine ways that further modifications could occur that would enhance the stability of the system.
Does Life Have a Threshold?
To summarize, Deacon argues that evolution is a matter of “progressive restraint”, and that more specifically, there are two basic steps in the transition from non-living material processes to life, each involving a new relationship to constraints:
the orthograde signature of thermodynamic change is constraint dissipation, the orthograde signature of morphodynamic change is constraint amplification, and the orthograde signature of teleodynamic change is constraint preservation and correlation. (p. 324)
I think the insight that large-scale order or shape can have opposing or contragrade effects on thermodynamic processes is an important one. Conformation plays a key role in biological processes, for example, in the specificity of enzymatic catalysis and in the binding of key substances to cell membranes. However, the distinctions between thermodynamic, morphodynamic and teleodynamic processes are not as clear-cut as Deacon implies.
Consider the autogen example again. While Deacon refers to its two individual components–autocatalytic networks and self-assembly into containment structures–as morphodynamic systems, they are quite different from most of the examples of this kind of process he provided earlier. In the case of convection cells, and other examples, there was some kind of energy being inputted into the system—heat, light, or the kinetic energy of moving air—which is key to creating an ordered arrangement (constraint amplification) in the system. If the energy is removed, the order immediately collapses.
In the autocatalytic sets and containment structures, in contrast, there is order already present in the system, existing independently of any need for energy input:
both autocatalysis and self-assembly are morphodynamic molecular processes that are capable of occurring spontaneously in a wide variety of conditions. What they share in common is a dependency on molecular shape-effects and a propensity for promoting rapid self-amplifying regularities. (p. 302).
In other words, while simple water molecules or molecules present in air have no tendency to organize in the absence of some unusual conditions imposed from outside, the somewhat larger and more complex organic molecules present in both autocatalytic networks and containment structures do not require external energy sources to organize. Given the presence of enough of these molecules in close proximity, they will organize spontaneously. One might say that certain characteristics of the molecule, in effect, take the place of a constant input of energy in creating the “perturbation” that results in organization. The needed constraints are built into each individual molecule.
This is a very significant difference. It means that the distinction between amplification of constraints, the key feature of morphodynamic systems, and their preservation, in teleodynamic systems, is blurred if not dissolved. In simple systems like whirlpools or convection cells, the organized water molecules can have no effect on the constraints that are necessary for this organization. They are completely isolated from the obstacle in the stream or the heat source. In this sense, we can indeed say that such systems cannot preserve their constraints.
But in any system in which molecules organize spontaneously, this organization in itself does not simply amplify constraints, but promotes or preserves them. Thus in the absence of any containment structure, the autocatalytic network may still form and proceed to cycle substances through a series of metabolic reactions. Conversely, the containment structure is capable of forming in the absence of an association with an autocatalytic network. Neither system alone may be as stable or as self-preserving as their combination. But the difference is one of degree.
This being the case, what exactly is the threshold that an autogen crosses? We can grant that it is the product of more constraints, and that it has processes that tend to preserve those constraints, but that is a quantitative, not qualitative, difference. Deacon also describes teleodynamic systems in terms such as “reciprocal complementarity” and “dynamic circularity”. Both of these terms, it will be appreciated, are basically synonymous with “synergistic” and with “constraint correlation.” Synergistic systems are those in which the constraints of one process correlate with the constraints of another—that is, the existence of each help maintain the existence of the other–and in this way are mutually self-preserving.
In other words, the shape or form created by morphodynamics has effects in creating other constraints that help stabilize itself. But such synergism clearly exists as well in the autocatalytic set, in that each substance is necessary for the creation of another, and is in turn dependent on another. The constraints of one metabolic reaction, by producing the catalyst for another, correlate with and preserve the latter’s constraints. In a word, each reaction is necessary for the whole; none is sufficient. Synergism is also present, at least in a mild sense, in the self-assembly process that creates containment. As the structure grows, the opportunities for further growth are enhanced, because the reactive edges—the points where further additions can be made to the structure–increase in length.
In fact, the organic molecules that constitute pre-living processes like autocatalysis and containment have other properties that promote synergism and self-preservation. For example, amino acids are zwitterions, meaning they possess two or more molecular groups that can ionize, creating opposite electrical charges. This enables them to act as buffers, that is, to stabilize the pH, or hydrogen ion concentration, of their immediate environment. Since most biochemical processes proceed at an optimum rate in some narrow pH range, this property can enhance the probability that a variety of teleodynamic processes occur.
So teleodynamic systems, as Deacon defines them, can be extended to include at least some of what he claims are “only” morphodynamic systems. If an autogen can be said to behave in a way that promotes its own preservation, so can its isolated components. The difference is quantitative, not qualitative. Autocatalytic sets and containment processes are not as efficient at preserving themselves as their mutual combination, but nevertheless can do so to some degree. And most important, they do so by the same general process of reciprocal or synergistic interactions.
What about simpler systems, such as convection cells? As I noted earlier, these are quite different, in that they are composed of very simple molecules such as water or the oxygen/nitrogen/carbon dioxide molecules in air. These molecules do not possess the ability to organize spontaneously in the absence of specific kinds of energy input. So they can be described as having general characteristics that are quite distinct from teleodynamic systems.
But most of the examples that Deacon discusses, including not only convection cells but systems featuring resonance set up by air currents or light, are artificial, are made possible only by human intervention. Whirlpools are natural phenomena, but of course no one would suggest that they formed a plausible step in the emergence of life. Still other morphodynamic processes discussed by Deacon, such as those that result in natural patterns found in seashells, pine cones, and animal skin coloring, account for certain properties of already evolved organisms, but again, do not appear to be capable of facilitating the transition between non-living processes and life.
So these simpler morphodynamic systems have limited relevance to the question of how biological function evolved. While they do illustrate how inputted energy can create order, this does not happen in biological systems without the critical help of special kinds of molecules that are capable of using that energy in ways that very simple molecules cannot. The road to life could not even begin without these molecules—and conversely, it could proceed to some extent in the absence of such extrinsic sources of energy.
Yet even prior to the existence of organic molecules, there is evidence of somewhat similar processes. For example, the reactions that form very simple molecules essential to life such as molecular oxygen, carbon dioxide and water “are capable of occurring spontaneously in a wide variety of conditions” just as Deacon describes for the morphogenetic processes of autocatalysis and self-assembly. Of course, the former reactions are far simpler, but the question is, how different in kind are they? These simple molecules are both formed and preserved by means of certain constraints. Moreover, water molecules are capable of further organization that is the basis of the liquid properties of this substance. Water as a liquid is further constrained, and promotes further types of reactions among molecules that can dissolve in water. The shape of individual water molecules, which allows them to bond with each other, is critical to this process.
Can Purpose be Defined Objectively?
To summarize, I’m arguing that the distinctions between thermodynamic, morphodynamic and teleodynamic systems are not as clear-cut as Deacon implies. The creation of constraints is evident even in very simple chemical reactions. There is of course no question that the processes become more complex as we consider what he calls genuine morphodynamic, then teleodynamic, processes, but this to a large degree is a difference in kind.
Does this really matter? If the kinds of processes that Deacon describes really occur, does it make much difference whether we consider their emergence as gradual or relatively sudden? I think it does, because Deacon is committed to drawing a fairly sharp line between non-living and livng processes:
If everything is ententional in some respect, then we are nevertheless required to specify why the absential properties of life and mind are so distinctive from the properties exhibited in the non-living world. We still need to draw a line and explain how it is crossed. (p. 40).
Deacon, in other words, while not accepting dualism, believes that the world appears dualistic to us, and that we must explain how this appearance comes about. Thus he describes teleodynamic systems as ones that “exist for the sake of preserving the integrity and persistence of these integrated systems.” They
do not merely react mechanically and thermodynamically to perturbation, but generally are organized to initiate a change in their internal dynamics to actively compensate for extrinsic modifications or internal deficits. (p. 487).
The problem with terms such as “for the sake of” and “actively” is that they are largely in the mind of the beholder, and thus not objective. It’s true that autocatalysis and containment processes, let alone simpler molecular reactions, can be understood in “passive” or “mechanical-thermodynamic” terms. Just add the ingredients and the reactions take off. But that is basically also the case for the autogen. As I noted in an earlier quote, Deacon concedes “that in one sense all change ultimately originates from spontaneous processes.” Spontaneous, in this context, means not free or unpredictable, but essentially the opposite: occurring under a wide variety of conditions, and therefore effectively inevitable. He makes the same point when he describes living processes as resulting from “falling into complexity”. (p. 457)
So where exactly is this line? Here is what I think is a sympathetic interpretation of Deacon’s thesis. From the beginning of existence on earth, if not earlier, there have been processes featuring constraints, creating molecules with a strong tendency to remain in their state. We do not ordinarily call such processes, or their products, purposeful. As these systems become more complex, however, involving shape effects as well as the interactions of several or more different processes, an increasing amount of energy is devoted to creating and preserving highly improbable states. We can call this a purpose, accepting that the line between purposeful processes and purposeless ones is fuzzy, just as is the line between life and non-living processes.
However, even if we concede this much–that purpose or function can be described in an objective manner—this still leaves a major gap in our understanding. It is not so much purpose that needs to be explained as the experience of purpose. This is the hard problem of consciousness, and I think Deacon misunderstands the distinction:
Reframing the concept of sentience in emergent dynamical terms will allow us to address questions that are not often considered to be subject to empirical neuroscientific analysis…Even the so-called hard problem of consciousness will turn out to be reconceptualized in these terms. (p. 487)
The hard problem of consciousness is a first-person phenomenon, not a third person phenomenon. Thus by its very definition, it is not something that can be described objectively, nor that is amenable to empirical analysis. Nor does providing an objective definition or description of purpose even bring us closer to understanding consciousness in this sense, any more than describing thermodynamic phenomena such as heat objectively brings us any closer to understanding our experience of heat.
Deacon seems to believe that because purpose or function is absential, it must necessarily help explain those aspects of mind or consciousness that also appear absential. But just because two different phenomena appear to be absent from physical processes does not mean they have a basic underlying similarity. And to repeat, merely by claiming that purpose is an objective phenomenon, one is conceding that it is something very different from conscious experience.
I understand why Deacon is so committed to taking this approach. Like most scientists, he sees no viable alternative in closing this gap between consciousness and the physical world. As I noted in the beginning of this review, the only alternative seems to be some kind of dualism, such as panpsychism. He considers this briefly, but rejects it because it seems to him to lead to a dilemma. If all forms of existence are conscious, why are some, such as human beings, far more conscious than others?
If the reason that human brains are a unique, intense, and persistent locus of absential properties (compared to rivers) is because they are differently organized, then organization is effectively doing all the work of explaining this fact. (p. 41).
In other words, if the greater degree of consciousness of human beings results from their much more complex brains, why is anything other than the brain necessary to explain consciousness?
But while there are some strong arguments against panpsychism, this is not one of them. Consider a simple metaphor. Imagine a variety of electric/electronic devices, ranging from the very simple—say, a light switch—to the very complex—a computer. The function of the computer, I think we can all agree, is much more complex than that of the light switch, and it is so just because of it’s structural organization—all the transistors and connections among them. In this sense, structure, or complexity of organization, is doing all the work in accounting for the differences in complexity of function.
But both the light switch and the computer share one critical feature that is necessary for them to have any function at all: the flow of electricity. Without electrical current, neither device, nor any other electrical or electronic device, functions. There is no ententionality or absentia at all without it.
We can extend the same metaphor using living systems. Consider what happens every morning of our lives when we awaken from sleep. Virtually instantaneously, we are conscious, aware of an external world of sights, sounds, and other sensory stimuli, as well as of our private thoughts, feelings, sensations, and so on. The scientific account of this is that certain neural pathways become activated. These pathways were present while we were asleep, but like the transistors in a computer or the wiring in a light switch, they lacked electrical activity.
So again, it is apparent that differences in structural organization—those in the portions of the brain that are activated when we are awake vs. those that are activated when we are asleep—underlie differences in our degree of consciousness. But there would be no consciousness at all, either of the waking kind or of the kind in sleep, if these neural pathways are not activated by electrical processes.
I want to emphasize that I am NOT claiming that consciousness just IS electrical activity. Electrical activity is just another material process, and fundamentally does nothing above and beyond structural organization to explain why we are conscious. But because we can make a conceptual distinction between the structure of the brain or a computer, and the electrical activity necessary to turn it on, the latter can serve as a way of thinking about how consciousness could depend critically on some fundamental property that is associated with structural systems.
So while the debate over consciousness will continue, I think we must firmly reject Deacon’s implication that panpsychism is impossible in principle. While it is profoundly unsatisfactory to most scientists and philosophers, because it seems to define the problem out of existence, I think one could say much the same about Deacon’s approach. Though he had provided us with a fruitful way of thinking about function or purpose in biological systems, it does not tell us anything about the much more difficult problem of how it is that we experience anything.