Culture, far from being some new trajectory of evolution (and, as posited by niche-construction theory, even a major new source of selection pressure), is evolved social psychology in action, feeding back to reinforce it. We become actually ever better at expressing our genes in evolving greater flexibility: the very opposite of the freedom Dennett contends evolves. Pinker and Dawkins likewise hold profoundly mistaken positions that we “transcend” our genes. A much more radical bottom-up conceptualisation of the social sciences is required; with psychology and sociology subsumed under systems-biology.
Responses by Joseph Carroll and Ian Roberts
Rejoinder by Steve Moxon
Culture Is Biology: Why We Cannot “Transcend” Our Genes—or Ourselves
Culture (whether human or of other species) is the manifestation of evolved psychology; and given that this is the product of the biological structure that is the brain, then culture is biology.
This might seem banal but for the observation that our behaviour within our cultures feeds back to reinforce the biology—optimising and making it more efficient. So it is that culture is very much a part of biology, not merely growing out of it to progress thereafter on an autonomous track.
Such feedback necessarily takes place, or why would our facility to create culture have evolved? (Human culture hardly resembles a Gouldian “spandrel.”) The relationship between any organism and its social system necessarily is a “hall-of-mirrors” precluding novel trajectory, and not just in the short-term (as I will duly explain).
Human culture is often, even usually regarded as being “above” biology because of extra-genetic modes of cross-generational transmission of cultural product, but an additional mode of transmission is of little consequence unless what is being transmitted is truly novel. For the above-mentioned reasons, it is not.
We can see, then, that Edward O Wilson understated the reality when long ago he pointed out that culture is always “held on a leash”  from biology, never escaping it. Yet Daniel Dennett, the philosopher who has most concerned himself with evolution, sees an actually weaker tie; substituting for Wilson’s leash an infinitely elastic cord. He believes, as in the title of his book-length exposition, that Freedom Evolves.  Certainly the facility to cognise and behave flexibly evolves; and given that this is instrumental to everything on which it is built, then it serves to make the human organism more efficient in interacting with its environment; not least with conspecifics. Consequently, biology and the genome encoding it, far from being usurped actually are still better expressed. In a non-trivial sense, therefore, we become ever more the slaves of our biology and our genes, just as we are provided with the illusion of being progressively freer of them. This fits within the overall trajectory of evolution: of a progressive increase in reproductive efficiency (which readily can be seen as the key contrast between humans and lowly classes such as bacteria).
As a philosopher, Dennett should know all too well that increasing flexibility of cognition and behaviour is the only meaningful sense of freedom that an individual organism can experience. Instead, he makes the leap to join Richard Dawkins and Steven Pinker in putting forward the line that somehow through our culture and our higher cognition we can (and do) “transcend our genes” (my paraphrase) and thereby our biology. Indeed, it amounts to a claim that somehow we “transcend” ourselves, which self-evidently is nonsensical.
It’s a bizarre position for arguably our three most eminent evolutionary thinkers to adopt. This is especially true of Steven Pinker, who, as the author of the book, The Blank Slate: The Modern Denial of Human Nature,  should be more keenly aware than anyone of the fallacy of placing humanity above nature. However, it is the usual view, notably shared by those who espouse any of the various ideologies of our culture. According to the philosopher, John Gray,  the various humanist ideologies in lauding mankind all betray how we are unwittingly saddled with the residue of Christian thinking; no parallel, he argues, being evident outside of Western culture. The “promised land” of Christian teleology, Gray sees as having secularised into an unacknowledged supposed causal agent pulling us towards some sort of utopia; in the process problematising “free will.” Gray singles out the philosopher of our illustrious trio: “Dennett … has spent much of his career labouring to show how scientific materialism can be reconciled with a form of free will—a project that would scarcely occur to someone from a culture not moulded by Christianity.”
The Dawkins/Pinker/Dennett axis is backwards, resting on the notion of “emergence”; that the philosopher Mark Bedau  sees as unnecessarily opening up a great explanatory gulf with lower-level processes (“emergence” likely being another case of problematising by philosophers). Their position, as I will outline, falls foul of systems-biology, the most basic understanding of the concept and theory of information, and contemporary evolution theory itself.
Steven Pinker memorably quipped that “If my genes don’t like it, they can go jump in the lake.” He was alluding to his decision not to spread his genes by reproducing. I challenged him on this from the floor at a symposium at the LSE in London. Surely an eminent evolutionary psychologist must well know that in this regard human motivation—that of the human male, clearly—is a proxy one of desiring sex, not desiring to reproduce per se; and that the use of modern contraceptive technology actually facilitates sexual activity? Doesn’t making professor, never mind such an eminent one, considerably increase appeal to women, both as a marriage and an extra-pair sex partner?
The Harvard professor has never said anything about eschewing sex, and the highly competitive behaviour of males with others of their own sex is (as Professor Roy Baumeister has outlined ) the key sex difference. Males compete for status in order to be selected by females, and therefore such competition is the principal instrumental behaviour to what Pinker claims he has in himself usurped—but which in any case he has not, having merely confused reproduction with sex.
I didn’t get an answer. Just a very long empty stare into the aisle between the two halves of the audience seating until the chairman moved on the discussion. Steven Pinker surely realises that far from adopting what he took to be a culturally derived imperative to replace how he would otherwise behave, instead he has been subject all along to the inter-related set of motivations we all share irrespective of the culture in which we happen to live. Does he imagine he can import into his brain a novel motivation? From where in the environment would this come from other than the mirror of evolved social psychology that is our culture; that is hardly likely, therefore, to throw up something new? And how does the professor envisage the motivational-set within his brain reacting other than by subsuming any such hypothetical import to further its own ends?
The failure of understanding by Pinker here goes deep, resting on a false schematic of the brain. And inasmuch as this reveals general truths about system and level that are applicable to the relationship between the organism and culture, then it is illuminating here to outline.
The author of How the Mind Works reveals a Cartesian dualist position in that very title, and evidently believes that he can control the rest of his “mind”—I will use the more appropriate term, “brain”—through certain higher-cognitive neural processing in his cerebral cortex. The truth is that the brain has evolved successive layers that function instrumentally to the layers below them, with the whole behaving as one system driven (in terms of initiating alertness) from the brainstem. There is no control centre.
The cerebral cortex facilitates complex integration of neural processing, incorporating sensory data from interacting with the environment, serving to modify behaviour so that it becomes more complex and indirect, the better to ensure the completion of motivation-behaviour loops. This does not mean that there is a locus of control within the cerebral cortex. Indeed, if we insist on any such identification, we would have to point to the afore-mentioned brainstem along with some other phylogenetically ancient structures associated with basic emotions; emotions being a visceral translation of basic motivation. Motivation does not arise in the cerebral cortex. Here arises merely neural integration that may contribute to the brain acting according to one or more key motivations over one or more others.
Our motivations, in functioning as a suite, at any one point in time feature one or more to the fore. If we are not being self-goaded to behave directly to bring about sexual intercourse and consequent reproduction, then we are being self-goaded to behave in some way instrumental to this eventuality. There is no “debating chamber” within the brain where some brain within the brain weighs up competing demands, as we imagine our conscious “mind” to be. What we call consciousness is an epiphenomenon of the integration of neural processing: the brain as a whole experiencing, after a delay, facets of its own working.
This simplest schematic of the brain showing the necessary relationship of parts to the whole as a system, and one that ultimately is “bottom-up” rather than “top-down”, is a contemporary systems-biology approach.  The causation is not circular as might be supposed—“developmental systems theory” posits circularity, but the theory fails through confounding development and evolution.  We falsely intuit downward-causation for obvious reasons, and have less trouble seeing upward-causation when we move away from the “conscious mind” and culture to the sub-organismic “major evolutionary transitions.”
Just as the application of a simple systems-biology perspective gives us a better overall view of how the brain works, it similarly improves our understanding of individual organisms vis-a-vis their social systems and cultural products.
Richard Dawkins takes a similar line to Pinker, famously writing that “we alone on earth can rebel against the tyranny of the selfish-replicators” . Dawkins would consider himself merely the “vehicle” for his genes, yet here he imagines he can drive off on some novel trajectory without genes being at root the navigation. From his own gene-centric theory, Dawkins would argue that the “vehicle” (or “interactor”, as some term it) is not primary because it is not the “replicator.” The counter to this view is, of course, that the “vehicle”/”interactor” is the entity that is “visible” to selection. And the chicken-and-egg issue of gene/organism is clouded by the recent systems-biology understanding of the gene as the gene-protein-cell complex.  But the gene-centric perspective is all-conquering in “population genetics.”
This is the way we need to look at the gene. Not in a simplistic abstract model of isolated genetic change at a snapshot in time within an infinite-sized gene pool, but collectively within the reality of the finite-sized, usually small reproductive group over time. This really does bring the social group into biology: through selection acting across different time-scales enabling the evolution of “policing” mechanisms against “selfish” traits, in what is termed “lineage selection.”
Leonard Nunney writes:
Lineage selection does not alter the fitness relationships of the traits; instead, it exploits variation in the genetic architecture of lineages to minimize the occurrence of the trait that is advantageous in the short term but disadvantageous in the long term. … Lineage selection reduces the likelihood of cheating over the long term provided lineages that give rise to cheats at a low frequency are more successful over the long term than are lineages that give rise to cheats at a high frequency.
The evolving of “policing” of “selfish” traits in this manner potentially could become so complete that all selection at the level of the individual ceases, and selection changes from within- to between-group,  so that we get group-selection as it is properly defined , as happened to create the “major evolutionary transitions.”  But as for the particular “particle”-”collective” relationship of organisms to the social group, this is extremely rare. It is thought that only eusocial insect species—and only one or two even of these—could fit the bill. In social systems, almost always selection operates on the organismic level to produce adaptation that is considered to be at most a “cross-level by-product” . There is no “super-organism” in higher-animals.
So it is that in studying even complex multi-tiered nested sociality in higher animals, Dawn Kitchen & Craig Packer  conclude: “Finally, we could find no compelling evidence that a vertebrate social system ever exceeds the sum of its parts … The most elaborate social systems … only require an ability to recognise a large number of individuals (rather than any form of group-level cognition).” … we see no reason to invoke anything beyond a simple set of individual decision rules.”
They see no such thing as “group mind.” Its absence is very apparent in computer modelling of dominance hierarchy formation,  which occurs by self-organisation given nothing more than the shared neural capacity of individuals to process what are known as “winner” and/or “loser” effects—the biasing of likelihood to contest in future based on the outcome of previous contests.
The upshot is that in higher animals generally, not just for humans, there is no supra-individual entity, let alone an autonomous one. The notion that culture is “above” biology looks terminally ill from whichever angle you look.
The sort of paucity of understanding exhibited by Dawkins/Pinker/Dennett reaches its apotheosis in “niche-construction”:  the recent theory that culture is a niche we create that becomes the major locus of selection pressure on the human genome—and, supposedly, a new form of selection to boot. This is held to explain the considerable recent evolution of human genes,  much of which is expressed within the brain. But rather than being the result of selection pressure from any human-created “niche,” this is likely the result of sexual selection. It is axiomatic in biology that rapid selection is caused by sexual rather than natural selection, and human higher cognition surely is under inexorable selection pressure to further integrate in the service of producing art and good conversation for courtship purposes. This is the basis of Geoffrey Miller’s “mating intelligence” theory:  that integrated higher-cognition is the perfect basis of signalling male mate-value given the susceptibility of the highly complex inter-related genetic coding involved to produce non-optimal or dysfunctionality (as in schizophrenia ).
“Niche-construction” theory is also a profound failure to comprehend basic information theory, as Tom Dickins has outlined.  The brain receives as input only that which it has been specifically prepared to look for. Inasmuch as it responds to environmental variability, this is contingent according to presets that have evolved in anticipation. The brain imposes models on the environment to suit its purposes; it is not the case that the environment somehow imposes itself on the brain.
Furthermore, Dickins shows that “niche-construction” theory is nothing less than a failure to understand the rudiments of contemporary evolution theory itself, in its positing a new form of selection that is in fact simply a re-statement of natural selection. And Dawkins points out —with the full backing of the European Science Foundation —that the theory is simply a re-statement of his long-held notion of “the extended phenotype.”
The emptiness of “niche construction” theory is shown by its inapplicability. Attempts to find support for it in contradicting the tenet of “adaptive lag” (the oft cited point that the human genome has not had sufficient time to significantly evolve since the Pleistocene) end in the sole regularly cited adaptation of the very minor physiological change that extends lactose tolerance from infancy into adulthood. No adaptation that in any way significantly changes human psychology has even been suggested. Evidently the scaling up of social group size has not required any psychological adaptation that was not already present. [This is hardly unexpected given that the key ability to form nested hierarchy is phylogenetically quite ancient, being exhibited by Cetaceans.]
“Niche-construction” theory is not only a mess of theoretical wrong-headedness, but it is in dire need of a reason as to why it was ever formulated.
Any view, such as “niche-construction,” of the supposed primacy of culture, contradicts the mature “bottom-up” system understanding provided by systems-biology, in merely assuming downward-causation on no basis other than the implicit acceptance of Durkheim’s groundless assertion that there are irreducible “social facts,” when all the evidence converges on culture being part of biology.
There is perhaps too much of a tendency within science to seek consensus at the expense of the bold “kite-flying” needed to spur and make real progress. We can see this in the often stifling peer review process, and even at symposia to celebrate the extension of the Darwinian revolution to the social sciences. Given our Western ideological bent that Gray identifies—which is the root of the dead hand of the post-modern [sic] imperative not to “privilege,” that appears to extend to scientific paradigm—it is natural that we should feel churlish not to attempt to build bridges with social scientists recoiling from the impending subsummation of their disciplines under biology. (We’ve seen the war in university anthropology departments as ascendant biology has riven them into biological and cultural halves.) But biological/ evolutionary approaches can’t be in bed with the old “top-down” paradigms of the social sciences, amounting as they do to little more than repositories of tired ideology. They are expressions of some of the very distortions of cognition and behaviour that form evidence for adaptation that biological/ evolutionary models cite.
To a future of a lead from biology / evolution theory in all disciplines involved in the study of culture that currently work “top-down,” we might all raise our glasses, toasting “bottoms-up!”
 Wilson EO (1978) On Human Nature. Penguin
 Dennett DC (2003) Freedom Evolves. Penguin
 Pinker S (2003) The Blank Slate: The Modern Denial of Human Nature. Penguin
 Gray J (2007) Black Mass: Apocalyptic Religion and the Death of Utopia. Allen Lane
 Bedau MA & Humphreys P (2008) Emergence: Contemporary Readings in Philosophy and Science. MIT Press
 Pinker S (1997) How the Mind Works. WW Norton & Co
 Baumeister RF (2007) Is there anything good about men? American Psychological Association, invited address. www.psy.fsu.edu/~baumeistertice/goodaboutmen.htm
 Noble D (2008) The Music of Life: Biology Beyond Genes. Oxford University Press
 Pradeu T (2009) Organism in Developmental Systems Theory (DST), PhilSci Archive http://philsci-archive.pitt.edu/archive/00004523/
 Dawkins R (1976) The Selfish Gene. Oxford University Press
 Noble D (2008) Genes and causation. Philosophical Transactions of the Royal Society A 366
 Nunney L (1999) Lineage selection: natural selection for long-term benefit. In Keller, ed
(1999) Levels of Selection in Evolution. Princeton University Press
 Gardner A & Grafen A (2009) Capturing the superorganism: A formal theory of group adaptation. Journal of Evolutionary Biology
 Okasha S (2008) Evolution and the Levels of Selection. Oxford University Press
 Maynard Smith J & Szathmary E (1995) The Major Transitions in Evolution. Oxford University Press
 Okasha ibid
 Kitchen DM & Packer C (1999) Complexity in vertebrate societies. In Keller (see next reference)
 Hemelrijk CK (2000) Social phenomena emerging by self-organisation in a competitive virtual world (‘DomWorld’). University of Zurich. Published online at http://www.ifi.uzh.ch/ailab/projects/collective/hemelrijkCELE2000.pdf
 Laland KN, Kendal JR & Brown GR (2007) The niche construction perspective: Implications for evolution and human behaviour. Journal of Evolutionary Psychology 5
 Laland KN (2009) Personal communication.
 Geher G, Miller GF & Murphy J (2007) Introduction: The origins and nature of mating intelligence. In Geher & Miller (eds) Mating Intelligence: Sex, Relationships, and the Mind’s Reproductive System. Psychology Press
 Shaner N, Miller G & Minitz J (2006) Mental Disorders as Catastrophic Failures of Mating Intelligence. In Geher & Miller (eds) Mating Intelligence: Sex, Relationships, and the Mind’s Reproductive System. Psychology Press
 Dickins TE & Dickins JA (2008) Mother nature’s tolerant ways: Why non-genetic inheritance has nothing to do with evolution New Ideas in Psychology 26; Dickins TE (2005) On the Aims of Evolutionary Theory. A book review of Odling-Smee JJ, Laland KN. & Feldman MW (2003) Niche Construction: The Neglected Process in Evolution. Evolutionary Psychology 2005 3 human-nature.com/ep
 Dawkins R (2004) Extended Phenotype—But Not Too Extended. A Reply to Laland, Turner and Jablonka. Biology & Philosophy v19n3
 European Science Foundation (2008) The New Role of the Extended Phenotype in Evolutionary Biology. An ESF Explanatory Workshop, Copenhagen, Denmark, 2-5 November.
 Dawkins R (1989) The Extended Phenotype: The Long Reach of the Gene. Oxford Paperbacks
to Steve Moxon
1. Joseph Carroll’s Response to Steve Moxon
Joseph Carroll is Curators’ Professor of English at the University of Missouri—St. Louis. He is the author of The Cultural Theory of Matthew Arnold, Wallace Stevens’ Supreme Fiction, Evolution and Literary Theory, Literary Darwinism, and (forthcoming) Reading Human Nature. He has produced an edition of On the Origin of Species. He is a co-editor of the forthcoming Evolution, Literature, and Film: A Reader. He co-edits The Evolutionary Review: Art, Science, Culture. He is guest-editor of this special evolutionary issue of Politics and Culture.
I think Steve Moxon is clearly right about the basic contradiction involved in declarations that we might somehow “transcend” our genes. The illogicality of that proposition seems to me on a par with the futile efforts, conducted over millennia, to attribute omnipotence to God and simultaneously to absolve Him of responsibility for evil. Squaring the circle, in both cases. And Steve is right too that such circle-squaring derives from religious or quasi-religious imaginative presuppositions.
I am impressed too by Steve’s clear and incisive formulation of the bottom-up structure of motivational systems in the brain (“emotions being a visceral translation of basic motivations”).
Though agreeing with these large contentions, I have reservations about some of the formulations used to support them. One reservation concerns consciousness; another concerns group-selection; and a third concerns sexual selection as the source of the exceptionally large and complex human brain. The three topics are intertwined.
Steve declares that “what we call consciousness is an epiphenomenon of the integration of neural processing.” This sounds a bit like Stephen Jay Gould’s hypothesis that the large human brain, with all its complexity, is really only an elaborate air-conditioner, designed to evaporate heat. It sounds even more like Geoffrey Miller’s hypothesis that the large human brain, despite all its functional complexity, and despite its obvious practical utility for many of the purposes of life, is really only an elaborate equivalent of the peacock’s tail, a hypertrophic and thus costly way of displaying good genes.
No, culture is “not above biology.” Culture is not “autonomous.” Does it necessarily follow, though, that “there is no ‘super-organism’ in higher animals”? I think not. In repudiating “niche-construction theory”—with a good deal of hyperbolic assertive vehemence— Steve argues that the only evidence ever cited for rapid recent human evolution is the “very minor physiological change that extends lactose tolerance from infancy into adulthood. No adaptation that in any way significantly changes human psychology has ever been suggested.” This claim is factually incorrect, and can thus not offer the needed evidentiary support for the claim that “the scaling up of social group size has not required any psychological adaptation that was not already present.”
Lactose intolerance is the most frequently cited instance of “gene-culture co-evolution,” but it is not the most important or basic instance. That distinction belongs to cooked food. Wrangham (Catching Fire) makes a strong case that this innovation predates the Pleistocene and is largely responsible for the extraordinarily rapid expansion (on the scale of evolutionary time) of the human brain. Nicholas Wade (Before the Dawn) summarizes a large amount of genetic evidence, including the evidence on the FOXP2 gene and the evolution of body lice (indicating the use of sewn clothing), indicating major changes in the brain over the past 100,000 years or so. Cochran and Harpending (The 10,000 Year Explosion) extend that kind of evidence into much more recent evolutionary history. Christopher Boehm (Hierarchy in the Forest), Richerson and Boyd (Not by Genes Alone), and Kim Sterelny (Thought in a Hostile World) all make cogent arguments that humans, using their expanded symbolic capacities, have within the past 100,000 years or so developed a layer of specifically social psychological adaptations involving “tribal instincts,” that is, the power of identifying with a social group that is itself defined symbolically, by means such as body paint and other forms of bodily ornament, and also by tribal traditions of myth and religion that create a historical narrative for the emergence and special character of the group.
The scientific arguments for the way people use symbols to identify themselves as parts of social groups converge with common observation. People live and die for national flags and religious symbols; they go into battle cheered on by their national anthems and encouraged by propaganda films, poems, and novels that display images of heroic self-sacrifice for the good of the group. Identifying ourselves with groups is so deeply ingrained in our evolved psychology that we can exploit it for the purposes of pure entertainment, as when we become loyal fans of sports teams. (In my neck of the woods, vast hordes self-identify as members of “Cardinal Nation.” Loyal followers of the Rams, though, these days, are scarce on the ground.)
Is consciousness “epiphenomenal”? A contrary line of argument is that consciousness provides the necessary means for generating specifically human forms of behavioral flexibility: for generating plans based on mental representations of complex relationships, engaging in collective enterprises requiring shared mental representations, and thus producing novel solutions to adaptive problems (Boyd, On the Origin of Stories; Carroll, Literary Darwinism; Dissanayake, Art and Intimacy; Dutton, The Art Instinct; Tooby and Cosmides, “Does Beauty Build Adapted Minds?” [SubStance 30 (2001): 6-27]; E. O. Wilson, Consilience). This line of argument posits no dualistic segregation of genes and mental events. It affirms that culture is indeed “part of biology.” It also makes sense of what is obvious to common observation: that we use symbolic images to guide our behavior.
The arts are a special subset of symbolic culture. Theories attributing an adaptive function to the arts come from various schools and emphasize different aspects of the arts, but they all work variations on a common theme. They all concentrate on the way the arts develop the mind, enrich its powers, and make it more capable of dealing effectively with its physical and social environment. Such claims might seem little more than common sense. We have all experienced moments in which some song, story, or play, some film, piece of music, or painting, has transfigured our vision of the world, broadened our minds, deepened our emotional understanding, or given us new insight into human experience. Working out from this common observation to a hypothesis about the adaptive function of the arts requires no great speculative leap. The arts help us live our lives. That is why they are human universals. In all known cultures, the arts enter profoundly into normal childhood development, connect individuals to their culture, and help people get oriented to the world, emotionally, morally, and conceptually.
2. Ian Roberts’ Response to Steve Moxon
Ian F. Roberts teaches literature and science, literary theory, and 19th century literature in English at Missouri Western State University. He is also Literature and Science Area Chair for the American Culture Association.
Steve Moxon is the only symposium contributor who touches directly on an issue that is, I believe, at the very heart of the antipathy toward biological understanding of culture. This is the hoary old problem of so-called “free will.” As Moxon points out, even Dawkins, Pinker, and Dennett sometimes speak, if only metaphorically, in terms that suggest some kind of mysteriously “emergent” notion of free will. Each of these thinkers is, in fact, quite capable of reconciling the sense of being able to act freely with a thoroughly causal-deterministic view of the world, more or less the same way John Stuart Mill did. However, Mill’s explanation of free will isn’t in the least libertarian or contra-causal. For this reason, it also fails to satisfy those people who insist that any free will that doesn’t somehow transcend physical causation just isn’t worth having or settling for. Those not satisfied with a biologically explicable free will, as opposed to some contra-causal and therefore supernatural form, recognize that the causal-determinism of biology is fatal to any notion of transcendent free will and, hence, to their popular notions of morality and culture. This is a more widely and deeply engrained source of resistance to biological thought than is generally recognized. It is also one which those who seek to integrate a more biological perspective into cultural analysis must confront directly and successfully if they are to make any significant headway. Until those in the humanities and social sciences are made to see that libertarian, contra-causal notions of free will are empirically and philosophically bankrupt, as well as unnecessary to the explanation of human behavior, antagonism toward biology as a source of cultural insight will likely remain stalwart (as I also argue in detail elsewhere)1. It is therefore necessary to exorcise the libertarian “residue of Christian thinking” that still possesses attempts to explain culture.
1 Roberts, I. F. (forthcoming) Free will, determinism, and moral responsibility in American literary naturalism. In K. Newlin (ed) Oxford Handbook of American Literary Naturalism. Oxford University Press
by Steve Moxon
That I’m making the crucial philosophical points to get the science right to facilitate the proper biological understanding of culture, is agreed by my respondents; indeed, Ian Roberts highlights this, and I appreciate his effusive words. Joseph Carroll agrees whilst taking issue with some of what I cite as manifestation or corroboration. I’ll confine my reply to these last, after first making a qualification I forgot to include re “downward causation.” I wrote that such a notion is mistaken, which indeed it is; but I should have made clear that I mean anything more than a trivial, everyday sense of the “top-down,” such as what is evident in Mark Bedau’s own example of the traffic jam.
My point that consciousness is not a property separable from the rest of neural processing does not make the brain any the less complex: it is merely a different conceptualisation. Not only do I not accept that I’m making any over-simplification, but the charge boomerangs back at those who perpetuate untenable mind/brain duality. This seems to be what Joseph is doing here, despite his prior concession that such a mindset is untenable. [Mind/brain duality is so ingrained that it tends to resurface as soon as it’s been buried.] “Mental representation” is the very sort of non-explanation that I dealt with. “Mental representations” are what we envisage as items of consciousness, so the argument simply regresses back to an argument about the nature of consciousness. To invoke “mental representations” is no more to explain neural functioning than is to posit a brain within a brain or Cartesian dualism; and indeed it looks like really yet another extension of the usual dualism.
A different conceptualisation also would be required of “group-selection” (“multi-level selection”), and one alien to just about all biologists, in order to make the claim that there is “super-organism” in higher animals. I take the state-of-the-art position on this: Samir Okasha in his masterly book-length discussion: Evolution and the Levels of Selection.
Regarding “niche-construction”: I stated that the only regularly cited instance was lactose tolerance; not that no other instances were ever cited; so I made no claim that was factually incorrect. Neither lactose tolerance nor the instances Joseph cites are material to the discussion, because they are not adaptations to change brain structures. The ability to cook food surely is just a cultural practice that was enabled by general flexibility of cognition and behaviour. Likewise the advent of clothing does not in any way indicate major changes in the brain. Habitation of significantly colder climate regions forcing the donning of animal hides to provide necessary insulation, presumably would be well within the capability of hominid general explicit cognition. It does not seem to require any specific form of cognition.
By contrast, for sure, group identification must involve social-psychological adaptation, but it’s phylogenetically very ancient, and consequently does not require the relatively recent brain evolution that “niche-construction” theory posits. As regards religion/myth, there is no evidence of any specific adaptation. It is generally accepted that religion/myth is simply a cultural product of general cognition – though this does not mean that these phenomena cannot serve specific functions such as, possibly, the need to signal “reliability” in a courtship context pending pair-bonding, for example. Symbolic capacity is another general rather than specific ability: to do with neural integration, which is itself a general cognitive evolution. This must have a far longer evolutionary history than the Holocene, and it does not follow that some specific selection pressure from the cultural milieu drove this. Likewise apparently the result of profound integration of cognitive processes, the arts likely function to signal genetic quality in mating contexts (which is pretty well every context in human sociality), as outlined by Geoffrey Miller in his “mating intelligence” theory, and as I mentioned. As Miller informs me, this fits with my own development of Wirt Atmar’s “genetic filter” theory of the function of the male sex (See my paper in Medical Hypotheses: “Dominance as adaptive stressing and ranking of males, serving to allocate reproduction by differential self-suppressed fertility: Towards a fully biological understanding of social systems.”) This would seem to be a progressive general evolution under sexual selection pressure rather than any specific cognitive adaptation. There is nothing here that “niche-constructivists” can point to in support of their theory.
The resistance to a supposed over-biologisation is so deep that abandoning the forward trenches is for some time bound to give way to merely falling back to reserve defensive positions. These are made of the same earth and form the same quagmire, so they are no more robust. The regression back to biology is relentless.