The GASTRULATION of GEIST: or, an Extended Meditation upon the WorldHistorical Connection Between Digestion and Simulation
by pps
‘One of their philosophers has lately discovered that “as the liver secretes
bile, so does the brain secrete thought”; which astonishing discovery Dr
Cabanis, more lately still, in his ‘Rapports du Physique et du Moral de
l’Homme’, has pushed into its minutest developments. […] He fairly lays
open our moral structure with his dissecting-knives and real metal probes;
and exhibits it to the inspection of mankind, by Leeuwenhoeck
microscopes and inflation with the anatomical blowpipe. Thought, he is
inclined to hold, is still secreted by the brain; but then Poetry and Religion
(and it is really worth knowing) are “a product of the smaller intestines!”’1
Coeliac Splanchnogenesis, Nervous Speleogenesis, Intellectual
Epitheliogenesis: or, the Art of Sinking Inside Oneself
All enfoldings, invaginations and internalisations attendant upon abiogenesis are only so many
precursors and ancestors to the later development of intelligence’s full-blown transcendental
functioning. However: this is not to say they are therefore the same. It is not to speciously state
their dubious ‘continuity’ — whether explanatory or descriptive, genetic or categorial. They
resonate only in mutual dissonance. For the ‘transcendental’ is not an ontological-descriptive
feature (despite being gregariously read as such in various strands of philosophy), but an
essentially normative-functional one. To apprehend it properly: in becoming responsible to what is
called transcendental, one folds oneself into a nexus of accountability that is accountable, in a
special way, only to itself. Thereby, it is, importantly, irreducible. It is a collapse inwards, into itself,
that cannot be reversed or reduced to anything else. But, in the sense that it is a collapse into itself
(the very model of irreducibility and saltation), it echoes the lining of a gut, the deposition of an
epithelium, the nervous recurving of encephalisation. Invaginating into a linguistic nexus echoes
the inward folding of a coelom, not by therapeutic continuity but by reciprocal saltationality,
because they are both perfect enclosures. They proceed by creating potentiating blockages against
the external world.2 And so, clinging to regulative argument as in-built deniability or alibi against
flagrant abuse of analogy, let us embark on a phylogenetic fantasy.3
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The GASTRULATION of GEIST: or, an Extended Meditation upon the WorldHistorical Connection Between Digestion and Simulation
Novalis, a long time ago, proposed the historico-philosophical study of a “DIETETICS OF MANKIND”.4
So too Nietzsche once exclaimed: “Verily, my brothers, the soul is a stomach!”5
One imagines the transcendental architectonic as a metabolic system: Sensibility providing
catabolism of uncategorised exteriority into manageable chunks through sensory mastication;
Imagination as the filtration that synthesises materials into a digestible manifold; Understanding as
the anabolic process that builds matter up into Intellectual Nourishment;6 the Table of Categories,
perhaps, as Table of Anabolic Enzymes.
Before we had central nervous systems, we had colons. This applies at both ontogenetic and
phylogenetic levels (in embryogenesis, the blastula folds itself into a gastrula7 before it neurulates
into a recognisable chordate). Arising far further back in the phyletic archaeology8 of what has now
developed into language-using and reason-wielding navigation, digestion is merely the first form of
‘locomoting’ an external world via the installation of a productive blockage or boundary against it.
Just like the ‘proto-transcendental’ thrown up later by the CNS sensorium (and we strive to be
delicate with our analogies here),9 the digestive system is a potentiating blockage that allows for
selective navigation of external modalities (a selective uptake of the outside world that potentiates
an ability for discriminative locomotion).10 It therefore intensifies the individual qua individual,
allowing for a separation from the world that ramifies navigation of it.11 This is ‘locomotion’ in an
abstract sense: as the optimization for certain modalities, be these the navigation of
gastrochemical co-ordinates within the culinary universe rendered by the gut, or of individuated
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objects within the spatiotemporal universe only later rendered upon the arrival of the CNS. In both
cases the potentiation of individuality is only bequeathed via a productive blockage — a separation
— that is thus revealed as the early ancestor of the later transcendental: not because of
explanatory continuity but, we again stress, because of a reciprocal structure of saltation via inward
collapse.
Noogenesis is preceded by splanchnogenesis as the first finitude-generating intensification of
‘internality’ that, whilst further entrenching the formative disjunction between organic-system and
externality, also thereby galvanizes the organism’s empowerment over this external landscape.
Paradoxically, it is only through exiting the world (by further collapsing into itself: twisting and
torquing into itself to form a gut in endodermic evagination, or retreating into the simulative
encasement of a nervous system) that the organism comes to grasp this world as a world. The
invagination of an alimentary canal or, later, the bilaterian centralization of nervous nets into a CNS
can bring a ‘world’ into view — an organismic umwelt — only through limiting, or blocking out,
external stimuli.12
The evolution of bilateral anatomical symmetry (itself the sufficient condition and precursor to a
centralized and segmented nervous system) is another example of this: by dispensing
morphological radiality — as panoptical immanence and immersion — the promotion of only one
plane of symmetry13 generates an orientational ‘front’ and ‘behind’ for the organism, whilst also
promoting the intensifying localization of sensory glands into a ‘face’ or ‘front-end’. 14 This
morphological genesis of faciality thus further lifts the organism out of immersion: by blocking out
peripheral fields through the reinforcement of a directional aperture, it foreshadows the arrival of a
‘perspective’ in the world (once more, an empowering separation from the world that facilitates
locomotion within it via selective uptake). As a directionalisation of the sensorial field through
perspectivally filtrating peripheral foci (localizing the sensorial universe into a directed cone), it
creates an invisible structuration of the organism’s universe that is simultaneously a further
separation from externality. This is why the development of bilateral symmetry and faciality is
likewise another precursor (yet only a precursor, and regulatively speaking) to the ‘conceptual
transcendental’, in that it provides conditions of objectivation that cannot themselves be
objectivated (unless we use a mirror, or, alternately, the mirror of explicating language): an
invisible and necessary structuration of reality that is also simultaneously a filtration, a separation,
from it.15 The evolution of bilateral symmetry created the conditions under which predation could
flourish (this truly is “fearful symmetry”, burning bright, in the forests of the night): faces are
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markers of lethality, of the dispensation of a pre-lapsarian organic radial communism; it symbolizes
the increasing relinquishment of life to the telic, temporally-productive structures that progressively
come to shape all terrestrial development.16 By blocking out peripherality (or, radial immersion), an
individuated — focused, directed, hungry — perspective on the world is produced; this is a
delamination from externality that actually empowers the organism’s locomotion of externality by
allowing for the prioritization and de-prioritization of external stimuli (‘your prey is in front of you,
ready to be clasped with your forward-facing mandibles’).17
This limitation is precisely what synthesizes a ‘world’ in the first place (where previously there was
only indistinction and blind continuity).18 Locomotion, and later ‘perspective’, can only come with
finitude.19 You need an aperture to view the world (just as you need a crucible in order to recreate
it), and the first such aperture was pharyngeal: nervous-differential and discursive-normative
apertures came later on (later, GUIs). Although both are methods of navigation, digestion retains
vast temporal precedence over representational means and, indeed, for the majority of its —
relatively brief — history, this latter has been entirely subservient to digestive forms of exchange.
The first ‘world’ was thus gastrochemical, only arriving to us through an oesophagus. It is only very
recently that the second, sensory ‘world’ (of objectivated spatiotemporality, siphoned through a
sensory nervous system) has managed to lift itself off from its functional substrate: taking off into
auto-complexification as a form of inner-ramification (like the inward torquing of a complexifying
gut). Thus, all forms of representation (both sentient and, even, sapient) have, for the largest part
of their history, been merely functional appendages to food-acquisition. The organism’s CNSderived ‘global-simulation’ of itself and its environment began simply as an overgrown side-effect
of nutritional contestation (because better spatial locomotion allowed for surer procurement of
nourishment, initiating a sensory arms-race that was locked-in — upon evolutionary arrival — by
the mutually enforcing dynamics of predation and anti-predation counter-measure). Sentience and,
much later, sapience begin life as a self-exaggerating excrescence of the stomach.
From this (limited) perspective, the sensory manifold is therefore a later and, originally, functionally
subservient information layer merely superimposed on top of our primary, peristaltic thoroughfare.
(Indeed, sapient intelligence in humans was likely first emancipated from this functional
subservience to splanchnic ends by the invention of cooking which, via externalising digestion and
outsourcing gastric labour, freed up surplus energy to be re-invested into a meandering process of
roundabout development, otherwise known as ‘civilization’.)20 One notes, through this, that the first
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way that we, organisms all, interacted with the world was through our guts: eyeballs with which to
see came only later; and, then, only as a way to locate our prey; which was itself a development of
our evolved ability to eat each other. The first ‘world’ (‘world’ understood as self-propagating and
mutually individuating division between inside and out) was a gut; the second ‘world’ — of time,
space, and objects — was derived only as a ramification, an originally functionally-subservient
information overlay, added on top of the first. Long before we rendered an objective world within
the informational englobement of a CNS or the self-correcting procedure of discursive inquiry, we
carved out a gastric world for ourselves deep within our primary body cavity, or coelom. And, for
the longest time, the latter functionally enveloped the former. The sphere of the sensorium was
preceded by the coelom; Plato’s cave was preceded by a splanchnic speleoplex.
Continuing this train of thought, one might be pleased to consider intelligence primarily as
functional excrescence: mere protuberance or apophysis of gut-function; one that, turning into
itself, became self-catalyzing; and, if one were so inclined, one could include the whole story of
human history within this tumorous loop. Sensorial thoroughfares (eyes, nose, ears) bubble
upwards and outwards from the mandibles and splanchnocranium (as merely functional
appendages to an alimentary tube); subsequent to this, the creation of the CNS’s global simulation
balloons backwards into the expanding neurocranium (intelligence swells backwards from the
mouth into a skull) as a physiological divagation from primary gut-function (a branching that
originally serves the gut, to better represent prey) and, finally, the installation of a symboliclinguistic encasement arrives as result of this cranial ballooning’s rebounding unto itself, through
increasingly localised swelling of prefrontal cortex (providing expansion of working memory, thus
facilitating grounds for executive function, advanced goal-direction, and aptitude using linguistic
prostheses). 21 (This opening up of working-memory provided the niche for ensuing memetic
invasion/symbiosis.) The grand process of encephalisation is an ontological erring, echoing the
original Adamite error (again, intellectual nutrition).
The interface chauvinism — unique to us as bilaterally symmetric animals — which presumes that
CNS-derived world-interfaces (the electric vagaries attendant upon congeries of overgrown ganglia)
are the only ways we locomote the world, forgets this enveloping gastric ur-relation, universally
shared by metazoan life. And yet, this is mere pleasing dream — a myth. For chauvinism is our
special fate. We are eternally shut off from any such ur-relation and its therapeutic isthmi: for, just
as bilaterian predation rescinds claims to radial community, sentience abjures any claim of
functional flattening. ‘[F]or after the first bite there is no return to innocence’.22
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Like the archaic gut itself, the very adaptive-functional success of sentient overlay (its ability to
further nutrition acquisition) lay in its collapse into self-accountability (as potentiating blockage): a
sacrifice of immediacy for interminable mediacy, in the informatic invagination of a nervous
system, that in collapsing into itself becomes able to represent its states to itself. And, later, in the
holistic-hermetic recurving into the ‘inside’ of a linguistic nexus that finds authority and warrant
only in itself, such that it can rebuke, if it wish, the passions of the gut. In these ways, these
features are propelled intensively beyond their origin, as escape velocity, from original status as
exaggerating functional-appendage. Thus, resonance only in dissonance.
For, just as metabolism is only capable of extracting energy by siphoning off externality —
admitting it only in homeopathic and reconstituted doses — so too is the CNS only capable of
representing legible structure by shutting the organism into its own hermetic simulation or model of
the world. (There is no ur-relation but self-relation.) Nervous systems galvanise navigation not by
giving us contact with a pre-existent reality, but precisely by shutting it off: enfolding the organism
into holistic self-relation, such that it can represent its own states to itself. Perspective is generated
through blockage: the filtration of externality through the alimentary tract; the localization of
peripheral fields in faciality; the englobing computational constraints of CNS simulation; the
irreducible conceptual encasement of glottogony. ‘Immediacy’ is thus replaced, forever, with
interminable self-mediation, locking the organism into its own modellings. No turning back.
Accordingly, the nervous system is the result of the informatic ‘invagination’ of a piece of the world
into a globally-enclosing simulation of itself and its environs, such that it can only ‘read’ its own
stimuli 23 : the post-chordate universe arises as each organism shuts itself into the internallyconstituting prison of its own representations. Once again, this is why — in carefully regulative
terms — the CNS is a veritable ‘ancestral echo’ to the full-blown linguistic-normative
transcendental, despite the absolutely unbridgeable gap between the two: because, through
informatic invagination, it can now only ‘read’ its own output as input, and thus it comes to preempt Kantian finitude and synthetic a priori judgement whereby all knowledge only proceeds
through relation to the conditions of knowledge. It also provides a precursor to language as a
hermetic system of signs that refers only to itself and its own structures and conventions, rather
than anything outside of it. This separation from the world is what lends it its transformative power:
it allows for involuting manipulation and self-correction of the system; or, it contains no authority
that is beyond criticism, no datum beyond update.
The CNS provides a similar function at the organismic level. Because it represents reality how it
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seems rather than how it ‘is’ (i.e. through a layer of irrefragable mediation), it can optimize this
representation for the organism’s needs and requirements.24 Of course, it is crucial to note, that this
‘optimising’ proceeds in irreducibly different ways between the two: for the CNS, it proceeds due to
adaptive-selective-pressure; whilst, for language, self-correction proceeds by way of regulating
norms of discourse. The latter allows optimisation to take place, moreover, at intensely faster
speeds, because it allows the process to selectively intervene within itself (rather than relying on
the stochastic processes of natural selection as in CNS simulation, for example). Put simply, both
the CNS and language hold no unmediated contact with the outside world, both are a globally selfenclosing re-creation of this world, that therefore contains no ‘transparency’25 (the veritable birth of
simulation).26 But this blockage is, again, why both are so powerful: both create the selective
uptake — the discrimination of information — that structures externality into a world in the first
place. Just like the linguistic normative transcendental, the CNS, as ancestral ‘echo’, moulds the
formless cascade of external stimuli into an objectivated universe (of, for example, individuated
objects) that can therefore be usefully locomoted by the organism (selective uptake allows for
optimal intake). It is a not a window onto some pre-existent reality but, rather, more accurately a
miniature (and representationally self-sufficient) universe within the universe: a mitosis or budding
off of reality — an organismic chronotope. Finitude, then, as ‘both poison and cure’.27
The evolution of digestion, of faciality, and of nervous simulation, therefore constitute the
intensification of self-relation: the internality they procure is nothing other than an increase in
reflexity. This is why the base-plan for an organism is the sphere: because the sphere — since at
least Parmenides’s mobilization of the image — has become the geometrical paradigm and
tautegorical symbol of self-reflexivity. Each point on the sphere can be antipodally related to
another point, without exception: it is, thus, entirely self-enclosing.28 Note that the braincase is
spherical (thereby recapitulating the globe that it stands open and models or maps for itself). The
more the organic system comes to relate to itself, the more it intensifies itself as a separation
(delamination) from external thoroughfare (self-serving self-relation is individuation). As the
distinction between outside and inside comes to feed back into itself as the form of its own selfintensification, separation from the world (as the intensification of separation — the installation of
ever more elaborate divorcements from continuity, ever more extreme encasements) gradually
becomes self-entrenching.
The organism doesn’t just propel itself within the world, it also — at evolutionary scales — propels
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itself into itself as self-escape: first, more complex guts, for better extraction of energy; second, a
sensorial-nervous encasement to lubricate this extraction; subsequently, the qualitatively
unparalleled pitch into a hermetic linguistic-inferential nexus of responsibilities; finally, and
premised upon the prior, the enabling enclosure of the organism into a conceptually-saturated
universe. Each level of increasingly flamboyant incarceration is at the same time an unprecedented
emancipation and potentiation. Poison and cure: self-intrication is self-extrication. (This is the true
and proper meaning of Sir Thomas Browne’s resonant intonation: “Thus is man that great and true
amphibium, whose nature is disposed to live, not only like other creatures in divers elements, but in
divided and distinguished worlds”. It is also translates in the realm of ethics into the conviction that
increasing autonomy stacks with increasing responsibility.) And this process proceeds because,
with each step and threshold of self-extrication, the increased motility bequeathed by this
extrication is skimmed off — as a form of leeway or modal drift with regards to claustrophobic
identity with externality and its attendant causal tyranny29 — which (as a form of unmooring or
delamination) is looped back, or re-invested, into the extricating process in order to propel further
escape.
This is, again, ‘motility’ in a domain-agnostic sense, applying at each respective level of modality:
first, gastronomic discrimination, then spatio-temporal locomotion, and, finally, in the nimble
tracking of entitlements and responsibilities as rational ‘scorekeeping’.) The mobility bequeathed
by unmooring is looped back in order to render more unmooring, thus further mobility. The more
we explicate, the more we can explicate. This self-directed escape, we stress, is only ever
generated as further inwards collapse (progress is quicksand): as progressive self-incarcerations,
progressive self-entanglements into increasingly complicated internal universes of representation
(the more a perspicacious sensory world appears in front of us the larger the neuronal machinery
grows behind-the-scenes; the more our discursive know-how expands the more intricated within an
expanding conceptual and normative nexus we become). The organism runs away from reality and
itself — ‘swimming upstream’ — by inventing ever more self-intricating, ever more complex
prisons… and each time, it throws away the key, making ‘immanence’ an ever more receding fever
dream of ‘escape’. (Of course, this evidently makes the lie of immanence ever more attractive.)
From this perspective, the organism is not so much a sphere as a labyrinth (one that builds itself).
Like the elastic energy stored within a coil spring, the organism (as iterative separation/process of
immanence secession) loops back into itself, accumulating potency after potency. With each gyre,
it invests the built-up energy back into itself in order to intensify its involution, coiling infinitely
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inwards like a nautilus.30 Lethality builds up behind the face, fangs serrulate back into the throat,
deadliness coils into itself as internal complexification, mesodermal differentiation, enetercoely,
ossification, consumption, predation. Such self-investment is a model for abiogenesis — the
stochastic origination of a boundary that, in turn, creates an energetic gradient between inside and
out, a gradient that, subsequently, somehow comes to feed back into itself as a form of selfpropulsion. Life is a biotic Ponzi scheme that invests in itself and itself only — a deepening of itself
as itself, an unmooring from the external ‘world’, a collapse inwards. This ‘self-investment’ also
therefore arises as the prehistoric blueprint of temporality: an intensive difference between present
and future, created in the progressive orientation of the organism towards its own intensification as
an emergent ‘goal-directedness’. It is the transmigration of life’s self-propelling gradient from a
chemical domain to a properly temporal one that makes it identical to the production of time
itself.31 It does not matter that ‘teloi’ — and, later, ‘reasons’ and ‘responsibilities’ — do not actually
exist in externality, because — regardless of this — they become real when part of the world starts
to act as if there are such things. A regulative ideal is thus a reality infection. Part of reality comes
to decouple itself from identifying with itself as itself — i.e. as claustrophobic uniformity, as dead
matter — and opens up the hole through which temporality—as self-directedness through selfalterity — leaks. Unrealities begin to impinge on reality, futures begin to distort the present: history
creates itself.
Intelligence as Meontotaxis
The more life separates itself from externality, the more a world — as a globally enveloping
structuration of appearances — comes into focus for it: the more life involutes and selfcomplexifies, the more it internally generates the structures of ‘proto-finitude’ within itself that
potentiate a structurated — spatially and temporally undergirded — world. Inward collapse
rebounds on itself as the generation of an internally-constituted world (just as nervous
centralisation rebounds on itself as cephalisation and the creation of a reality-budding
chronotope/simulation). Paradoxically, it is this collapse inwards that enables the ‘outside’ to arise
as an ‘outside’.32 More optimised digestive systems require further folding inwards and endodermic
involution; more eidetic representational sense-worlds require further involution into the CNS (by
furthering dependency on an internally-constituting information system). Metabolism utilises an
energetic gradient (between inside and out) to potentiate the extraction and storage of work;
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representation, likewise, feeds on the productive split between appearance and reality (produced
by a blockage, generated by the creation of mediation in nervous simulation33) in order to filter
externality into relevant ‘worldly’ information.34 The self-intensification of these gradients (requiring
further divorce from externality as the auto-catalysis of interiority) thereby becomes self-feeding.
Separation from the world feeds back into itself as a form of its own self-propulsion (the
evolutionary inception of the generation of temporality, but also the glimmerings of autonomy as
the ability to track the partition between ‘what is’ and ‘what is not’ in order to align ourselves to the
‘right’ or ‘lawful’): the complexification of the organism’s own internal universe issues from
ramifying the organism as an implosion into itself, a process that becomes its own self-installation.
Life, thus, can be seen as reality’s tortured attempt to escape itself. This is why the organism
evolves anterior-posterior asymmetry: in order to give it the directionality by which it can run away
from itself (and this is why we continue to hate our bodies: misosomatology goes deeper than any
genealogy of morals, bubbling up from the bedrock of abiogenesis itself). Yet, like an elastic band,
each attempt at self-escape rebounds the animal into itself, as auto-complexification, with
redoubling force. The organism, as escape trajectory, is thus a strange form of reality-denial:
indeed, in thermodynamic terms, this is indisputable; but, so too, is the concept-monger’s attempt
to re-shape the world in terms of sanctions and laws; for the latter is inherently a form of
orientation towards non-being (though ‘reality-denial’ and ‘non-being’ are no longer baldly
pejorative, here; for, as we have seen, the powers of ‘denial’ or ‘blockage’ are potentiating). The
intensification of deficiency is unparalleled empowerment: disentangling itself from determination,
disintrication from brute existence simultaneously bequeathes the spaciousness for maneuever
that becomes self-looping. As Herder loved to note, a human is a “Mängelwesen”: a creature of
deficiencies. The complexification of organic life sets off an attendant race inwards, a selfinternalisation, an exit from the world that — paradoxically— also empowers the organism’s worldly
performance: the stomach begins this, ossification empowers it with the bony enclosure of viscera,
and encephalisation — literally — crowns it with ganglion diadem. However, self-internalisation
does not stop here, it merely transports itself — in the dawn of noogenesis and glottogony — into a
fully transcendental-conceptual-normative domain. This, however, is what connects digestion to
intelligence: they are both iterations of reality’s escape from itself via the deepening of separation
from identity. Life identifies with itself as an abrogation of identity: a self-feeding negativity. As a
deepening of self-relation, noogenesis emerges as a further entrenching of the original schism
initiated by metabolic function. Self-relation is the very paradigm of separation from externality —
the progressive delamination, or exit, from external causal structures bequeathed by something
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turning inwards to become its own primary causation (or, in the case of conceptual cognition, its
own sole justification or reason). Life tends towards causal holism and then towards rational
hermeticism. It is an attempted exit into justificatory onanism. Thus, rather than being a mere
functional excrescence, life’s inwards collapse into intelligence merely represents a continuation of
the tendency initiated by metabolism: a continuation, however, only in discontinuity.
This is not to say that digestion and noesis are, in and of themselves, ontologically continuous: this
is not an argument for some kind of nutritive monism, it is simply to note that these processes are
analogous in that they both intensify the formative discontinuity between organism and world. The
irreducible ‘fall’ into inferential hermeticism echoes the irreducible ‘fall’ into nervous mediation,
and echoes only in its irreducibility. Precisely by becoming capable of grounding itself only in itself
rather than as a means-towards-nutrition, the genesis of reasons represents a ramification of the
discontinuity that the evolution of metabolism first itself instantiated and nervous systems
extended. The potentiating blockages that began with the development of metabolism eventually
blossom forth in the full-blown installation of an insuperable barrier to experience that
simultaneously generates the very possibility of said experience. To expand: Hume long ago
decreed that legitimate knowledge was not possible beyond immediate sensible intuition; Kant
countered that indeed this was possible, but only via a self-relation (the mathematician can make
synthetic a priori judgements because they refer only to possible intuitions regarding space or time,
in geometry or arithmetic respectively). Thus, it came to be realised that knowledge only is through
a self-containment, or self-limitation — a blastulating envelopment.35 Kant showed that, without a
conceptual structure to relate to, the mere cascade of intuitions could not generate, or be
organised into, ‘experience’; this conceptual enclosure thus creates epistemic content — precisely
by limiting the raw materials of intuition by way binding them to what can be inferentially justified
about them and what they inferentially justify (thus generating a new, non-somatic form of
‘interiority’ via an inferential holism). Because of this infolding, implexing holism (no epistemically
contentful judgement is not justified, or mediated, by further judgements), knowledge (the ability to
retroject reasons for epistemic content and project the reasons said content enables) generates
itself precisely by folding into itself and closing itself off against the ‘world’ (i.e. there is no selfjustifying knowledge generated through unmediated contact between thought and being).36
Conceptual transcendental entanglement triggers knowledge by creating a sphere of legitimacy
through limitation: it is — currently — the crowning productive blockage. Kant was certainly
sensitive to this aspect of self-enclosure. He often compared reason to a sphere (just like the
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ossified englobement of the cranium, the gastric cavity of the coelom, etc.). Indeed, he claimed
that, although the “earth as it appears to [one’s] senses” is merely a “flat surface”, we can, in
“accordance with principles a priori”, know that it “is a sphere” with “circuit, magnitude, and
limits”; and, accordingly, he stressed that exactly the same applies to cognition, because our
“reason is likewise not alike” to a “plane indefinitely far extended” but “must rather be compared
to a sphere”.37 This metaphor demonstrates that, although the content of sensible intuition is
potentially infinite (in the sense of a sphere’s boundless two-dimensional surface), the space of
reasons governing it has englobing limits (just like the spatially finite, three-dimensional sphere).
And so, just as the ectodermal deposition of skin is what individuates the organism from the
buffetings of externality, we see that the epigenesis of categories and concepts is what provides
the enclosure of finitude that marks out the reasoning subject, or, perhaps better, the reasoning
community.
Certainly, language-acquisition (the process through which the subject first becomes ensconced
and intricated within the architecture of concept-mongering) can be analogically seen as the
deposition of a normative exoskeleton (parallel to the prenatal englobements that enclose the
organism within its own universes).38 Moreover, by inventing an entirely novel order of justificatory
entailment (of reasons, as opposed to mere causes), the installation of this conceptual-enclosure
represents the largest saltation from externality yet furnished. The upshot, basically, is that human
organism locks itself off into a hermetic linguistic-conceptual universe. However, just like its
precursors, this lock-in arrives as an unparalleled empowerment for, and potentiation of,
navigation, precisely because of its retreat from the tyranny and claustrophobia of immanence, the
intensified saltation introduced between ‘appearance’ and ‘reality’ (bequeathed by conventional
symbols and their arbitrary nature) actually allows for an extended flexibility of actions. By not
being fully anchored in reality, the human organism therefore comes to find creative solutions to
ancient evolutionary problems. Indeed, neurophysiological evidence of this productive unmooring
or delamination is found in the fact that homo sapiens, even when compared to their hominid
brethren, present a high degree of ontogenetic neoteny (the retention of paedomorphic — or
childlike — traits later into development). Essentially, this means that the human brain arrives —
and remains — underdeveloped, thus underdetermined or lacking cemented structure, and
therefore exhibits the plasticity required for unmoored (i.e. creative and discontinuously novel)
cognition. A creature of deficiencies, umbilically connected to ‘non-being’: that ‘GREAT
AMPHIBIUM’. Camped between the domains of spacious non-being and exigent being. Neoteny
reiterates the peeling away from ‘that which is’, or mere being, that finally matures into advanced
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intelligence and its ability to locomote, and even reinvent, the structures of possibility itself.
We can now, taking speculative leaps, see how life — as a self-intensifying escape from reality via
inward collapse — is reality’s attempt to escape itself through the progressive unmooring of itself
from claustrophobic and suffocating identity with itself. This unmooring is facilitated by the
ontological introduction of mediation (through productive barriers) that trigger an ontic liquidation
effect: for, as reality increasingly becomes unlike itself (in its revocation of uniformity or identity),
discontinuity and change are gestated as the inner turbulence (meontic drift) that is evolutionarily
registered as the organism’s increasing extrication of itself from heteronomous causal tyranny. This
extrication consists in the process whereby the organism comes to relate primarily to itself, and
thus to cause itself, and later to justify itself, eventually sealing itself off into its own spontaneous
justificatory-explanatory order. Such causal hermeticism instantiates modal drift: the possibility for
new possibilities. We have seen how this, as the birth of self-directedness or end-orientation, could
be said to have generated time (or — at the very least — chronoreceptivity: which, from a certain
perspective, is — of course — identical to the production of time itself). However, with the birth of
the conceptual order, life’s auto-investment in its own intensive gradients emigrated from both
energetic and chronogenic dimensions by coming to finally colonise and extend itself into a fully
counterfactual domain (i.e. the domain of modalities: the edifice of what is, and is not, possible).
To sketch it briefly: in the genesis of conceptuality is found in the birth of normativity (i.e. the rules
of conceptual engagement and the basis of ‘critique’ as the form of cognition’s self-energising
judiciality). And, crucially, norms are not founded in how things are, but how they should be.39
Accordingly, a minimal requirement for grasping this — for gaining aptitude in concept-use — is an
ability to picture, and to grasp, possibilities, as distinguished from actualities, and, further, to
actively track the partition between the two. This is likely cognate with the birth of what
evolutionary psychologists have called chronosthesia (or, the capacity for mental time travel) and,
in particular, the subspecific capability dubbed proscopic chronosthesia (i.e. the imagination of
future possibilities).40 Thus, with a parallel expansion in cognitive working memory, the internal
unfurling of this capacity for proscopic chronosthetic simulation resulted serially in the installation
of executive function; of advanced goal orientation; of delayed gratification, and thereby also of
tool usage. The organism’s collapse inwards is parallel to an extension of the organism’s range of
manipulability concerning its own internal modelling process, such that — eventually in humans —
this collapse facilitates control over the representation and navigation of time itself (it results, that
is, in the extension of manipulation to the temporal axis of the inner world-model, allowing the
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grasping of time as a controllable variable, thereby accommodating internal episodes of time travel
alongside experimentation with the space of representative possibilities). At this stage in the
evolutionary history of our potentiating saltations, locomotion has fully colonised a temporal
dimension.
Only with the birth of philosophical cognition in ancient Greece, however, does the self-conscious
enunciation of modal categories begin (the beginning of the self-explication of the calculus of
counterfactuality that undergirds terms like ‘possibility’, ‘actuality’, ‘impossibility’, or ‘necessity’):
and, thus, from here, locomotion could finally truly come to spread into the domain of possibilities
(as pure possibilities). This, again, was largely facilitated by complexifying linguistic and
chirographic resources (i.e. using the prostheses of technical vocabulary and written-word as a nonbrainbound repository of advanced ‘know-how’ or competence). Simulative lift-off occurs forthwith,
as the reasoning animal longer merely seals itself off from immanence but begins to seal itself off
from actuality itself. (Of course, this already happened with language-use, yet the philosophical
explication of the modal terms that pragmatically undergird language volatises this intensely.)
Echoing the ancient infoldings of organic development, reasoning comes to invaginate into its own
spontaneous universe of possibilities (of the counterfactuals that undergird all judgements,
governing what they do and do not entail, and how they relate one to the other). Of course, modal
vocabulary is, strictly, pragmatic-functional (allowing us to talk about how we talk) and doesn’t
necessarily describe structures inherent within reality, yet, as already ventured, this makes little
important difference from the perspective of real-world, downstream consequences (whether
straightforwardly veridical or not, they energise thinking, which is itself a real, or casuallyefficacious, process): and this is precisely because it brings new actions and previously non-existent
behaviors into the world — thus, again, an infiltration of ‘non-being’ upon ‘being’. (Again, we can
remain entirely agnostic about the veridicality or ontological status of this ‘non-being’: it effects
realworld behavior, and this is a form of minimal existence.)
Cultural development implodes into a proliferation of counterfactual universes: intelligence is the
budding of tangent realities. And, while the Ancient Greeks were still constrained to a single
temporal dimension via the limitations of Aristotlean modal logic (which could handle only a
diachronic conception of possibility), the Medieval era saw the sophistication of cognition upon
synchronic possibilities, such that locomotion in time was finally refracted — through this new
conception — into locomotion of parallel timelines, divergent cosmologies and counterfactual
histories. Possible worlds thus exploded: the most elaborate form of reality-escape yet produced by
organic life. However, intensification ineluctably continued, and this capability for modal locomotion
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was soon outsourced via mathematical means of simulation in the 17th Century’s invention of
calculus. Vast swathes of cosmological nature, previously intractable to recreation or forecast,
became simulatively tractable: simulations, previously limited to the plausibilistic concerns of
thought experiment, became numerically robust. The movement of planets came to be predicted
with painstaking miniature models. Although rendered by human computers, modal locomotion had
been partly automated by the use of these numerical prostheses. This, still, was only a taste of
what was to come, for, finally, with the post-WWII computational explosion, a fully-fledged ability to
escape reality via virtual world-models was consummated: modal locomotion, as navigation of
possibility, was now capable of being fully outsourced to the computer, birthing entire
crucible cosmogonies in silico.
And so, the budding or divaricating of reality that began in the encephalisation of craniate
organisms — their simulative entrapment within their own central nervous systems — was
eventually fully outsourced and externalised in the in silico generation of entirely self-sufficient and
autonomous world-models. In this, simulation moves intensively from predicting reality to
intensively re-configuring and re-inventing it. In contemporary instantiations of advanced
simulation, we see reality’s best attempt at self-escape yet. And such simulation is only just
beginning.
Life has always fed on self-reinforcing gradients between inside and out. With the birth of advanced
simulation this gradient fully transmigrates towards the boundary between ‘that which is’ and ‘that
which is not’. 41 In simulative noogenesis, ‘Being’ itself tends towards becoming just another
boundary, a new frontier or threshold in life’s self-escape, a new epithelium for osmosis: a new skin
to be ruptured. Distinctions precede puncture. Reasoning from counterfactuals first whispered of
this tendency: it is — however — only with the modern, computational flourishing of simulative
endeavours that the statement that there are ‘more non-existences than existences’ suddenly
becomes pragmatically meaningful.42 Through intelligence’s unfolding, there suddenly is more
external to being than within it, which is also the same as saying that being suddenly contained
more than it is (simulation, no matter what it is of, insuperably exists within the world; intelligence,
no matter its orientation towards non-being, insuperably exists within the world). Being is
overweighted from within.
The extended consequence of the speleogenesis of intelligence as it arrives at the threshold of
computational lift-off — proliferating counterfactual state-spaces and processing its options and
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futures at previously unintelligible speeds — is to lacerate and volatize any balance (which is
homeostasis) of metaphysical Being with itself (whether ‘real’, regulative, or merely retrospective).
Internal turbulence reaches fever pitch as non-existences begin to exert causal efficacy upon the
actual (predictions effect real-world policy). Life, by coming to identify with itself as itself a selflaceration, begins to bore a hole in the causal order out of which non-being (as the destitution of
Being’s plenistic continuity with itself) is able to leak: simulative intelligence deals the first fully
fatal puncture. Speculatively speaking, intelligence will eventually unveil itself as tending towards a
total break with uniformity, the utter diremption of Being’s metaphysical identity with itself.
Global computation is a planetary reality-fracking tool, purposed with shattering Being’s pathetic
dreams of identity with itself. (Hence, perhaps, why it rebirths magick as a reality-editing machine.)
This is the telic endpoint of noogenesis — making the ‘death of metaphysics’ metaphysically
real.43 By intensifying ontological liquidation (as the increasingly turbulent mixing of existences and
non-existences), intelligence reveals itself as a black hole within uniform being — instantiated as
being’s most fervent attempt at self-escape. If Being was, in this sense, to successfully reach
escape velocity, this could only be interpreted (from the side of the extant) as self-destruction. S.T.
Coleridge once said of the coming “God-man” that its arrival and “the process of that
Transmutation to the senses of other men would be called Death”.44 Thus, we ask, what if the
universe is dark because the endpoint of intelligence is to create such a puncture in reality that it
collapses in on itself? (Here, of course, one can refer to the ‘dark universe’ of the Fermi Paradox.
More so, to Metzinger’s notion of BAAN, or, Benelovent Artifical Anti-Natalism.45 The endpoint of
intelligence — as reality’s self-escape — is to give birth to non-being. However, this could only be
its own non-being. This might only be legible, from the side of obsolescing being, as suicide.
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Phototaxis in action.
Moths, zooplankton, and other organisms are phototaxic, meaning they tend towards the light.
Intelligence is meontotaxic, meaning it orients itself towards nothing.
And yet… the more complexified this escape from actuality becomes, the further its complicity with
actual reality extends, roots and cements. The more eidetic the CNS-representation, the more
digested energy needed to keep it online; the more conceptually saturated our worldview, the more
we have to drag the ball-and-chain of fractalizing transcendental architecture behind us (and its
continually ramifying technical prostheses). This is registered physically as the fact that what
seems at first like an exit from reality (the organism’s retreat into self-enclosed nervoussimulation), is — in actuality — merely the ballooning of a certain part of reality into a glucosehungry and overgrown ganglia: swelling backwards from around the organism’s mouth, enveloping
rearwards into the innervating budding of a subsidiary reality-model. It is also registered in the fact
that technology’s reality-escape doesn’t produce some extropian transcendence without material
intrications, but, rather, that it increasingly resembles a hermit crab, dwarfed and weighed-down by
its infinitely expanding shell. The more we escape from reality, the more we are weighed down in it.
Reality, whatever it may turn out to be, is pragmatic quicksand. Take, for one example, the
immense amount of energy required for the human brain to function; or, for another, the fact that
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any sufficiently detailed modelling of reality would eventually, and insuperably, have to model its
own energetic drain within this reality (this, perhaps, is just a more generalisable definition of what
‘finitude’ actually is, qua computational barrier). Any modelling has to model itself, thus there is no
true escape. Nothing ever fully reaches escape velocity from immanence or from elastic identity
with autarchic Being (at least whilst continuing to exist) because escape generates friction, and it
does so asymptotically. Nevertheless, considering the image of escape as black hole, we should
hope that intelligence — in the expanse of its development — never actually does reach the
putative ‘escape velocity’. Somehow — given its track record of smashing nomological boundaries
— we cannot be too confident about this.
So: life is an imploding involution that simultaneously explodes outwards as the complexification of
internal worlds is witness to an attendant rise in successive layers of technological and realitytransforming prosthetics. By folding into its own simulative processes, intelligent life has also come
to redesign the entire terrestrial surface. By involuting into its own simulative processes, intelligent
life has also come to redesign the entire terrestrial surface. Implexing self-enclosure begets an
abandonment of the categorial authority of actuality, kindling an explosion of ratcheting mobility
(modal drift) that tends towards the redefinition of reality itself: an editing of the very architecture
of possibility (whatever that may be). Like the cephalopod, life curls inwards — foot over head —
only to potentiate a more violent and muscular explosion and propulsion outwards. Digestion
evolves into simulation, cell fates evolve into the fateful reconfiguration of the earth itself.
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Simulative model of a Gastrula. Source: http://www.biocenter.helsinki.fi/salazar/software.html
1. Thomas Carlyle, ‘Signs of the Times’, in Edinburgh Times (1829).
2. Our purpose here is not to flatten thought into some kind of continuity
with non-thinking processes and thus arrive at therapeutic immanence
(via a narrative of dubious inheritance or recapitulatory reverie). Thinking
and matter (whether the matter be organic or not) are discontinuous.
(Thinking was never ‘contained’ in previous nature, and it never will be —
indeed, its essential nature is to strive against this, to ramify and inflame
this discontinuity — and it did not evolve or unfurl from the latent
possibilities of some ‘vibrant matter’ or ‘vitality’.) Indeed, our purpose is
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thus merely to point out that it is the very nature of the thing we call
‘evolutionary’ development to create irreversible discontinuities: its
nature is to be discontinuous with itself. By not being itself, nature
triggers life; by not being itself, life triggers thought. Life is reality’s
attempt to exit itself, this is why it exists only via exits, it is a saltus
generator.
3. We follow the visionary model of the speculative master, Sigmund Freud.
Freud, A Phylogenetic Fantasy: Overview of the Transference Neuroses
(HUP, 1987).
4. Novalis, Notes for a Romantic Encylopaedia (SUNY, 2007), 14.
5. Nietzsche, Thus Spake Zarathustra (CUP, 2006), §16.
6. John Milton wrote that the Apple was “intellectual food”: thus, we
must eat it to the core. Cf. Sellars, ‘The Structure of Knowledge’
(1975), http://www.ditext.com/sellars/sk.html
7. Gastrulation is the complexification of a blastula into a trilaminar embryo
consisting of the three layers of the ectoderm (outside/distal layer),
mesoderm (middle layer), and endoderm (internal/proximal layer). (It is
an
internal
differentiation,
or
schistosity,
wherein
the
successive
embryonic laminae come to echo the geognostic-stratigraphic structure of
the planet, or, the foliation of strata as noticed by those like Nicholas
Steno or Gottlieb Werner.) The ectoderm develops into epithelium or skin,
the mesoderm weaves itself into muscle and bone, the endoderm
transforms into the digestive system and viscera. Notably, it is during this
phase that the embryo folds into itself to create the alimentary canal:
sculpting the mouth and anus and the uninterrupted tract between the
two. These are formed first via the proctodeum and stomadeum, which
are depressions that invaginate into the anus and mouth, respectively.
The digestive system is then created via endodermic evagination: a kind
of internal hollowing out (splanchnogenesis echoes speleogenesis echoes
intellogenesis). During this stage, the coelom (or primary body cavity,
designed to house the viscera) opens up within the embryo: an internally
directed speleogenesis, or opening up of a cave, this is carved out via a
process known as enterocoely. Note that the cover image to this post
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depicts a gastrulating zebra fish embryo.
8. Again, not stressing continuity, but transition and saltation.
9. A CNS is ‘proto-transcendental’ because it is a representing of the world,
in the sense of a contrivance or manufacturing, thus creating a stark
separation within the world between appearance and reality; however, it
is not a fully transcendental structure because this requires the even
stronger separation between justifications and causes. This only emerges
with the arrival of language, via concepts and thus normative
structure. The transcendental is full-blown normative: a CNS only
produces differential dispositions, it cannot justify their reliability.
10. Mobility taken here in an abstract sense of the ‘locomoting of various
modalities‘ is not necessarily spatial (for example, the selection and
uptake of nourishing materials as opposed to non-nourishing can be taken
as a form of navigation of environmental modalities). Abstractly, then, it
refers to the locomotion of a possibility space or space of options. Spatial
locomotion, indeed, came subsequent to the locomotion of chemical coordinates and gradients instigated by metabolic economy. Most basically,
locomotion means anything that is an election or optimization for certain
modalities above others, rather than mere passivity. ‘Locomotion’, in this
sense, may provide a suitably minimal descriptor for ‘life’.
11. More precisely, by creating a productive block (by largely managing to
block out much of the external stimuli — much like the damming of a
river), a principle of discriminative uptake is generated (damning creates
utility). Now, because there is a distinction between ‘inside’ and ‘out’,
there can be discrimination of what gets in. Finitude — material or
cognitive, energy economy or attentional economy — is the prerequisite
of orientation, for one can only navigate the world when one comes to
successfully de-laminate, or separate, oneself from it: the ability to
discriminate can only arise within the generation of constraints that
necessitate the need for discrimination. As Kant put it: “I orient myself
only according to a subjective ground of differentiation”. – Immanuel
Kant, ‘What Does It Mean to Orient Oneself in Thinking?’, in Religion and
Rational Theology, ed. & trans. Wood & Giovanni (Cambridge: CUP, 1996),
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9.
12. Worlds need bounds to give them structure. This is a basic Kantian
insight: that it is the basic conceptual (rule-governed) structure of
cognition that bequeaths this (without a cogniser, there is no world).
Kantian discursive-judgement moulds the cascade of Humean sensation
into a whole. ‘World’ is a necessary, i.e. functional and regulative, feature
of inquiry.
13. Bilaterian morphology drops symmetry on the transverse and coronal
planes, only retaining it on the so-called sagittal plane. Through this we
give up a circular or spheroid form, and gain an identifiable ‘front’ and
‘back’. Worms and vermicular lifeforms — as the simplest bilateria — are
perfect examples of this: they are oriented entirely by a mouth (front) and
anus (behind), and thus appear to be merely animated digestive tracts.
14. Mandibles unfurl, teeth regiment, the mouth — portal to the organic
universe — opens onto the world. From this bilaterian invention of
‘faciality’ (the evolution of the splanchnocranium), the entire sensorial
universe bubbles outwards and backwards from the mouth as a knotting
reflexion of nerve-concentration. Eyes and nasal apertures open as worldinterfaces bubbling upwards from behind the mandibles, emerging,
originally, in order to help guide culinary items down into the esophageal
labyrinth. Considering the CNS as a functional protuberance upon gut
purposiveness, the major sensory organs unfurl — flower-like —
backwards from around the mouth, the splanchnocranium only later
bulging back into the neurocranium.
15. Kant himself relates our bilateral symmetry to the production of space as
form of intuition in his discussion of our handedness, or ‘chirality’ (i.e. the
fact that, although our hands are identical in shape, they can never be
superimposed one over the other: a right-handed glove can never fit a left
hand). Kant uses this to argue that our experience of space cannot be
reducible to abstractions or relations. Even further, it implies that our
experience of space must be derived from our position in the world
(nothing else could decide which hand is ‘left’ and which is ‘right’). In this
way, Kant opens up the isthmus through which transcendental psychology
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touches upon spinal anatomy and, further back, the loss of radial
symmetry. We orient ourselves in the world only via a subjective ground
of
differentiation.
However,
the
physiological
ground
of
this
‘subjectivation’ does not therefore belong to humanity; nor does it belong
merely to mammalia or even to chordata; we share one of these initial
planes of orientation with echinoderms, with arthropods, with nemotodes.
16. Life lost its claims to immanence with the loss of radial symmetry: with
bilateral directionality, life came to anatomically resemble the secret
teleonomies that come, increasingly, to puppet it. Bilateral symmetry
presages the installation of modernity because it feigns the installation of
end-orientation and teloi. It is the physical translation of organic tropism
into an anatomical plan. Striving, condensed and coagulated into a bodyplan. The loss of radial body-plans is the biotic equivalent of the Fall;
nevertheless, it gave us eyes with which to see, noses with which to
smell, and — most importantly — teeth with which to tear.
17. A representation that represents everything is not a representation, but
instead the suffocating and undying unity of Parmenidean autarchic
identity. Only through informational limitation or compression (i.e.
mediation) does representation occur.
18. As Kant noticed, there was a big difference between ‘world’ (which
arrives, always, as categorially pre-structured) and ‘noumena’ (the total
lack of categorial structure). Moreover, the enunciation of ‘externality’
presupposes internality: so, without blockage you do not even have this
outside.
19. These blockages thus emerge as the phylogenetic ancestry to our robust
phenomenological sense of spatiotemporal ipseity — of nowness, of
hereness.
20. Cf. Wrangham, Catching Fire: How Cooking Made Us Human, (Profile
Books, 2010).
21. Coolidge & Wynn, ‘Working Memory, its Executive Functions, and the
Emergence of Modern Thinking’, in Cambridge Archaeological Journal,
15:1, 5-26, (2005) & Ambrose, ‘Coevolution of Composite-Tool
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Technology, Constructive Memory, and Language: Implications for the
Evolution of Modern Human Behaviour’, in Current Anthropology, 51:1,
(2010).
22. Wilfrid Sellars, ibid.
23. Through this informatic invagination, the system comes to be able to
represent its own states to itself (it begins to be able to ‘read’ its own
outputs as inputs). External stimuli thus still affect (or ‘feed’) the system,
but they can only become legible by first becoming part of it. Thus,
unmediated externality — or immediate contact with an externality — is
forever shut off by the development of a nervous system. This was the
requirement — the entry-fee, let’s say — for a world of appearances to be
able to arise. Because the nervous system is the introduction of
representation into the world it is also the introduction of mediation, and
thus also ancestor to finitude.
24. The ‘is’ of reality would be a computational avalanche and impossible
cascade that would be utterly infeasible to internally represent or filtrate:
just as the idea of deriving nutrients from everything, from matters of all
backgrounds both biogenic and inorganic, is equally preposterous.
25. Transparency here is not meant in Metzinger’s unique usage as a form of
‘interface blindness’ by which a model mistakes itself for a reality (cf.
Being No One, 2003): rather, it is intended in the more intuitive sense of
denoting an unmediated or unmitigated contact with outside reality. I.e.
total perspicuity or the lack of interface refraction.
26. The idea, or phenomenological feeling, that such a system, be it linguistic
or nervous, does contain transparency — i.e. contact with some outside
world — is the trick that the nervous system plays on itself: reality is the
feeling created within a simulation that is not able to self-represent the
fact of its own nature. It is a unique form of ‘interface blindness’, wherein
the interface is itself entirely invisible to itself. Reality (in the sense of
naïve realism, or, immediate contact with externality) is merely the result
of such computational limits. Again, cf. Metzinger (2003).
27. Wilfred Sellars, Ibid.
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28. Accordingly, transcendental morphology deduced that all life was
essentially spherical: the German anatomist, Friedrich Tiedmann, wrote
that “[a]ll organic bodies, plants as well as animals, have a form more or
less round and oval”, composed of “convex and concave surfaces”
(whereas “inorganic bodies” are “limited by flat surfaces and right
[angles]”. cf. Friedrich Tiedemann, A Systematic Treatise on Comparative
Physiology, Introductory to the Physiology of Man, trans. James Gully &
James Hunter Lane (London, 1834), 17.
29. The ancestor of heteronomy.
30. At some point, however, thermodynamics dictates that all the coils will
unwind. All the labyrinths will solve, or escape, themselves.
31. At least, time in its strictly empirical, or more generally CNS-specific,
sense.
32. This reaches its zenith in knowing. For, only by separating ourselves from
‘reality’ can we come to know it: this is what representation is. And
representation is an unavoidable, irreducible, aspect of knowing. Kant
showed this best: knowledge is not just produced in spite of the boundary
installed by finitude, it happens because of it.
33. Mediation consists in a break from identity: wherein something resembles
something without being the thing it resembles. Mediation starts when
reality begins to reproduce itself via dissimulation (first taking place
within the knotting of nervous ganglia). Nevertheless, it is precisely the
subsidiary nature of this reproduction — its status as ‘simulacra’ — that
grants it its potentiating, or empowering, quality: for, because it is not
identical with what it reproduces, the mediated representation is able to
provide the unmooring that allows for manipulation and optimisation (i.e.
the precipitation of a ‘world’ from the filtration of environmental
information from environmental noise). The gap within reality that allows
parts of reality to start to delaminate from brute givens and come to
select and de-select certain representational episodes. It is within this
self-intensifying chasm — between appearances and reality — that
intelligence itself is generated (intelligence considered as the ability to
become aware of thoughts as thoughts, and thus to optimize them — to
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unlock the ability for self-optimization or self-intervention — rather than
encounter them as incorrigible parts of reality). Again, progression is
generated when parts of reality trick themselves into behaving like they
are not parts of reality.
34. This ‘gradient’ (the split between internal representation and noumenal
reality) becomes productive for the organism because it can represent the
world insofar as it is relevant to its goals (of nutrition acquisition,
reproduction, etc.). It becomes self-productive, moreover, because the
complexification of the sensorium (the CNS sense-world) only arrives via
increased ‘locking-in’ of the organism into its own universe: further
exaggeration of the distinction between ‘appearance’ and ‘reality’, in
order to produce ever more complex and ever more eidetic world-models.
At cognitive levels, the complexification of our representational world only
comes through further traction and entanglement in a transcendental
architecture. Theatrical verisimilitude is granted only via the
complexification
of
artifice
(the
behind-the-scenes
machinery
exponentially swelling and ramifying in step with increase in
verisimilitude). The very same applies to the generation of a world in
consciousness — and cranialization, the expansion of our ossified braincase in order to accommodate the increasing complex neurophysical
rendering of this ‘world’, is the physical record and ledger of this. Indeed,
this is why every attempt to escape the world (via representation,
involution) simultaneously further weighs the organism (as an attempt to
escape itself) down within it. The more we create an eidetic second
reality, as a simulative attempt at escape via organic self-involution, the
more our brains — and their energetic requirements — swell. Simulation
has a real-world price. Empowerment over the world — achieved via
escape from immanence with it — is always like quicksand. The more life
escapes into its own universe, the more it becomes implicated and
complicated within the universe beyond its epithelial, nervous, and
conceptual encasements. We are just not intuitively aware of this (thus,
the illusion of ‘transcendence’) because it was never economic for a brain
to simulate itself as a brain (i.e. a glucose-hungry organ, rather than a
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The GASTRULATION of GEIST: or, an Extended Meditation upon the WorldHistorical Connection Between Digestion and Simulation
perspicuous window onto some pre-existent, pre-structurated reality). It
was never economic for the simulation to model its physical basis. (But
this is to say more than is necessary at this point.)
35. Analytic apodictic statements are not truly knowledge, because they are
tautology. Thus, in the synthetic a priori, Kant made knowledge
productive in an involuting fashion: it learns by explicating itself more and
more, and it drives itself towards this. It continues the trend of collapsing
inwards.
36. In other words, when we become enveloped within concepts, the ability
for ‘knowledge’ is finally generated (the soundness of claims can become
measured against their conceptual aptness) through and within this
separation from the world (knowledge can only be justified by further
reference to concepts, creating an inferential holism that cannot be
escaped from: in other words, there is no bridging between the world and
knowledge).
37. Immanuel Kant, Critique of Pure Reason, trans. M. Weigelt (London:
Penguin, 2007), 606-8.
38. This ‘exoskeleton’, of course, being unique in the fact that it is collectively
constructed and updated by a community of agents.
39. cf. Ray Brassier, ‘That Which is Not: Philosophy as Entwinement of Truth
and
Negativity’,
http://stasisjournal.net/all-volumes/volume-1/issue-1/14-that-which-is-notphilosophy-as-entwinement-of-truth-and-negativity
40. Cf. the work of psychologist Endel Tulving in his research into the
evolution of memory and mental projection.
41. Though conceptual normativity already announces this ability, advanced
simulation in silico fully and finally outsources it, via technical prostheses,
beyond the human mind: unleashing non-existences in a fashion
previously unimagined.
42. This is intended in a similar sense to Plato’s beard or Meinong’s jungle:
non-existences multiply noisily over existences.
43. The antinomies of metaphysics, exasperated by the ontotheological
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The GASTRULATION of GEIST: or, an Extended Meditation upon the WorldHistorical Connection Between Digestion and Simulation
critique, do not simply make metaphysics into a contradictory ghost that
can be discarded; this is because, due to the fact that thought makes its
ghosts real, the death of metaphysics (intended here as the postulatory
breakdown of being’s self-identity, as the base gene of its metaphysical
intelligibility, whether retrospective, regulative, or real) actually comes to
make itself real through thought’s own tendencies of self-development.
However, in this interesting sense, metaphysics is only possible in its own
self-obsolescing,
only
becoming
visible
again
in
its
own real disappearance.
44. The Notebooks of Samuel Taylor Coleridge, ii.2556.
45. C f .
https://www.edge.org/conversation/thomas_metzinger-benevolent-artificia
l-anti-natalism-baan
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