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This article was downloaded by: [Gazi University]On: 18 August 2014, At: 06:25Publisher: RoutledgeInforma Ltd Registered in England and Wales Registered Number: 1072954 Registered office: MortimerHouse, 37-41 Mortimer Street, London W1T 3JH, UK
Neuropsychoanalysis: An Interdisciplinary Journal
for Psychoanalysis and the NeurosciencesPublication details, including instructions for authors and subscription information:http://www.tandfonline.com/loi/rnpa20
The Symbolic Species: The Co-Evolution of Language
and the BrainWilliam Hans Miller
a
a12304 Santa Monica Blvd., Suite 210, Los Angeles, CA 90025, e-mail:
Published online: 09 Jan 2014.
To cite this article:William Hans Miller (1999) The Symbolic Species: The Co-Evolution of Language and the Brain,Neuropsychoanalysis: An Interdisciplinary Journal for Psychoanalysis and the Neurosciences, 1:1, 130-135, DOI:
10.1080/15294145.1999.10773254
To link to this article: http://dx.doi.org/10.1080/15294145.1999.10773254
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130
Jeannerod, M., Mouret , J., & Jouvet, M. (1965), Etude de
Ia mortricite oculaire au cours de Ia phase paradoxale du
sommeil chez Ie chat.
Electroenceph. Clin. Neurophys-
io1
18:554 566.
Ramon Greenberg M.D.
11 Waverly Street
Brookline MA 02146
e mail:
r m o n ~ r e e n e r g
hms.harvard.edu
The Symbolic Species: The Co Evolution Lan-
guage and the Brain
by Terence Deacon. New York:
Norton, 1997, hardcover 29.95, paperback
15.95
A few years ago the UCLA neuroanatomist and psy
chologistHarry Jerison asked, What is so great about
being smart? with the implication that in our species'
history, it is hard to conclude that our intelligence and
our capacity for complex symbol use has done us more
good than harm. What is ironic and prophetic, as Ter
ence Deacon shows us in his extraordinary text, is that
symbol use itself may be the only means available for
shifting the balance toward a kind
of
positive outcome
for ourselves, if not for the planet. The more we under
stand about the nature and origin
of
our symbolic ca
pacities, he claims, the better we can regulate our
enormous cognitive potential. He wrote his mystery
novel, as he calls it, with this goal of increasing our
understanding about how symbol reference and lan
guage came about, and ultimately,
of
who we are.
For about a year several UCLA linguists, psycho
analysts, and psychologists and I met weekly, reading,
discussing, and debating The Symbolic Species:
The Co Evolution Language and the Brain. We all
concluded that this is a profound work, remarkable
for its scholarship and extreme detail, and deserving
dedicated study. Here, I will sketch out a broad and
oversimplified overview
of
Deacon's complex evolu
tionary scenario, and then discuss a few of his essen
tial arguments.
Somewhere in our fuzzy past there were groups
of australophithescines who had already been bipedal
for some time and who could communicate with con
text-bound gestures and sounds. These foraging homi
nids lived in the savannas of eastern and southern
Africa. We can only marvel that they survived at all
in what must have been a continuously perilous envi
ronment. Except for their nascent evolutionary edge
of symbolic reference, we might very well not be here,
or might not know it. The time was about 2 million
years ago; it had taken several more million years to
get to that point from the great bifurcation that split
Book Reviews
man-to-be from the great apes. Then, something very
strange happened. A shift in cognition, specifically in
abstracting capacities and learning by logical and se
mantic categorization, began to dominate the experi
ence
of
these individuals and groups, which hitherto
had been limited by mental representations
of
stimu
lus-response associations to the mostly local context
of
rewards and punishments. Environmental events al
ways had signal value about how to react for all ani
mals, but if a new waterhole was associated with the
possibility
of
reduced thirst, the only condition that
guided the approach behavior of prehominids was the
appraisal of immediate safety. But with a doubling of
brain size in what was to be a shift from australo
pithescines to true hominids like Homo habilis (tool
man), a new condition and option became possible.
With improved cognitive hardware the hominid could
apply a system
of
divergent ideas and images based
on principled rules. Homo habilis felt the urge to ap
proach water, but instead of drinking, might con
sciously wait for an animal to drink first, then follow
the animal to see
if
the water was deadly or safe to
drink. A logical theory had been conceptualized and
tested. Many of his or her vertebrate ancestors could
learn the stimulus-response associations that, together
with instinctual responses, made survival possible. But
this hominid and his kind also could learn
the
system
of relationships of which these correlations were a
part. If this individual's logical experimentation al
lowed for survival and offspring later on, he or she
could then carry the gradually developing genetic pre
disposition for flexible rule-guided behavior into the
next generation. Remarkably, in the initial nonre
sponse, the stimulus to approach water was intention
ally used against itself. He or she delayed gratification
conditional upon reasoning, thinking, planning, vicari
ous trial-and-error, long-term memory all
of these
nonautomatic capacities. This was possible because of
a simple but effective gestural and guttural system
of
rule-based and communicated labels for objects and
actions developed within groups
of
individuals. The
neurobiological substrate for this advance in everyday
experience of early hominids was actually not new;
many primates can do a bit
of
this
if
given enough
training and exposure in a controlled setting. But for
more advanced hominids, it became a primary prob
lem-solving tool and the natural thing to do. In its
fullest developments it would provide humans with
an
unprecedented sort of autonomy or freedom from
the constraints of concrete reference.
The neurobiological cause and consequence for
this symbolizing capacity, according to Deacon, is the
property of an expanded prefrontal cortex (PFC) in
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higher primates and especially in man, which itself is
but a part of the unbroken continuity between human
and nonhuman brains. But back to our hominid an
cestors. When that semiotic boundary between local
(iconic and indexical) context control of behavior and
arbitrary (symbolic) conditional responding was sur
mounted on a regular basis, the hominid line, nearly
suddenly in geological time, applied symbol use
to
the
expansion of communication, complex speech, and
then full grammar-based language. These adaptations
further enhanced the existing primate dorsal-heavy
hominid cortex and its subtle perceptual biases that
could now generate the kinds of sounds and rules re
quired for a social system of communicatedmeanings.
But language and the rules (grammar) were never in
trinsic to the human brain; the only intrinsic factor
was the perceptual-learning bias. Language existed
then and now as a social phenomenon or as
memes [T]he brain co-evolved with respect
to language, but language has done most of the adapt
ing. So for this strange new way
of
communicating,
grammar was essential for later complex language, but
was its consequence, not its intrinsic cause.
On the way to developing full language, problems
of male provisioning, fidelity promises (marriage), and
group cohesion were solved, giving hominids like ar
chaic Homo sapiens and Homo neanderthalensis the
edge they needed to successfully compete and continue.
(Andbecausewe re here and they are not,
we
canprob
ably assume some kind of brain-over-brawn superior
ity, althoughDeacon thinks Neanderthals were
so
equal
to us in intelligence that the difference was probably
that
of
sheer numbers or plague survival.)
The brain, language, and culture of today, so ho
mogeneous in all the important ways, all developed
by oevolution Natural selection did most of the work
to produce the australopithescines, up to 2-plus million
years ago. But then the new trick of symbolization
and abstraction produced an overpowering adaptation,
reasoning and planning ahead, that changed the selec
tional context itself within which natural selection was
operating. In the case of brain and behavior, this new
type of selection, called Baldwinian, was no longer
, natural or simply Darwinian. Hominid selection
became directed by constrained actions. Thus greater
symbol use selected for greater PFC size, which ex
panded auditory-verbal capacities, which selected for
greater symbolization, and so on. For example, the
midbrain reticular areas, especially the limbic-peria
queductal gray circuits, allow only indirect cortical
motor control over the 30 to 40 primate calls that com
municate indexical signals
of
danger, food, and other
131
social transactions. With increased motor and prefron
tal cortex in hominids due to the sequential demands
of nonsymbolic gestures and speech, manual dexter
ity, and social interactions, adjacent cortical areas
gradually assumed direct control over the subcortical
arousal anatomy and behavioral sequences. This new
cortical displacement of neural connections became
both the cause and a consequence
of
the increasing use
of
vocal symbolization. This advance in turn improved
communication, putting further adaptive pressure on
the development
of
an even greater variety of vocal
ization, resulting in the innervation
of
the tongue from
the hypoglossal nucleus and a descended larynx, faster
consonated speech, and more complex vocal social
interaction (such as the ability to employ subtle decep
tive speech). At present we have sobbing, sudden
laughter, gasping, groans, and sighs as remnants of
subcortical control by midbrain structures; in other
cases after about age 3 we have the option to volunta
rily (cortically) regulate our vocalizations. This dy
namic circular neurobehavioral causality is
coevolution and runaway symbolization. Every im
provement altered the neurological and external envi
ronmental forces that then selected for a more
successful genetic host. This manner
of reasoning is
how Deacon can claim this strange thought: I suggest
that an idea changed the brain. But Baldwinian logic
sorts it out:
The
remarkable expansion of the brain
that took place in human evolution and indirectly pro
duced pre-frontal expansion was not the cause of sym
bolic language but the consequence
of
it.
Yet symbols themselves are not inherited and are
nowhere in the brain, even though there is a thresh
old below which symbolic processes are not possi
ble. Symbols evolve socially within the community
of
symbol users and are then borrowed as needed by
all. What is inherited is the capacity for plasticity to
change the circumstances
of
evolution and within life
time adaptations. The personal capacities for symbol
formation itself are also overbuilt for fail-safe learning
by natural and Baldwinian selection, to provide for
extreme cases
of
conceptual problem solving. Ergo
our ability to perform tasks like differential equations
which no H. habilis or H. erectus ever needed to solve.
Ergo our capacities for employing symbols to be con
scious
of
a personal self (subjectivity), the experience
of others consciousness (empathy and manipulation),
and fears of purposelessness and death. For symbol
ization is the means of justifying great acts of inhu
manity and kindness, and of religious solutions for
fears, and for comprehending symbolizing itself, as in
self-reflective consciousness. Deacon says it best:
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3
The
best and worst of what it means to be human
arose with the dawn of symbolic abilities. Thus sym
bolic reference underlies everything we consider
human: [T]he computational demands
of
symboliza
tion not only was the major source of selection pres
sures that could have produced the peculiar
restructuring of our brains, they are likely also the
indirect source for the selection pressures that initiated
the prolonged evolution
of
an entire suite of capacities
and the propensities that now constitute our language
instinct. And, selection for anything that benefited
this prerequisite function would have been constant
and intense throughout, including severe reproduc
tive costs in cases of failure to acquire symbols.
But this tidy narrative, like the journey of man
from there to here, gets quickly convoluted. The trail at
times is downright thready,
as
Deacon pursues lines of
logic, neo-Darwinism, molecular genetics, cell popula
tion dynamics, practically the whole history of neuro
science, comparative psychology, neural networks,
paleoanthropology, personal fancy, and more on the
way to building his massive case for the new phyla,
Homo symbolicus. Profound questions are raised in ev
ery chapter, andanswers are suggestedthat quickly pro
voke even more difficult questions. But Deacon
is
relentless. Happily, all the themes and subroutines in
this book revolve back on Deacon s three overarching
questions about man s unique cognitive style and lan
guage. These issues, which also constitute Deacon s
goals andwhich were anticipated by the opening narra
tive, are: What are the differences in the ways humans
and prehominids and animals reference information
and communicate in groups? Why do animals have so
much difficulty overcoming the barrier to symbolic ex
perience and communication? How do humans func
tion with symbols so easily and so early in life?
The first issue introduces the sine qua non for
understanding Deacon s book. He recounts the work
of
the late nineteenth century logician-philosopher
Charles Peirce in defining symbols and describing
symbolic referencing as the apex of cognitive evolu
tion
so
far. Peirce (1994) was concerned with the ways
we
find
meanings in a hierarchy
of
increasingly ab
stract references to objects, relations of objects to each
other, and to the family of concepts that are referen
tially based on these real-world foundations. In this
semiotic system, icons referred to the surface com
monalities between objects and the real things to
which they refer. Thus a statue of the
Buddha
really
looks like him. Indexes, on the other hand, stand in
dynamic causal relationships to their point of refer
ence and always refer to the associations, correlations,
Book Reviews
and implications for action that link them back to their
icons; the statue is thus also an indexical sign or signal
for certain kinds of behaviors and attitudes. And
fi-
nally, symbols refer to indexes and other symbols that
exist by arbitrary, conceptual and stable rules of inter
pretation within a group
of
individuals. Here the Bud
dha statue evokes the same rule-based meanings for
all those who share its conceptual relevance.
Peirce himself went to great lengths to establish
a 10-level hierarchy of transitions from the most iconic
reference (like the feeling
of redness )
all the way
to the highest symbolic level of logical syllogistic ar
guments. For simplicity Deacon chose to discuss only
the icon, index, and symbol. But given that one of the
most difficult problems in the book is the attempt to
explain the transition from indexical to symbolic func
tioning in early humans, it might have helped his case
if Deacon could have included more
of
the transitional
steps that Peirce defined.
Deacon s second and third goals are an under
standing
of
just this transitional puzzle: to comprehend
why nonhuman primates have so much trouble get
ting it, getting beyond immediately context-bound
stimulus-response cognition, and grasping the rules
that make possible generalization based on logic
(which grammar-based language requires). Many
pages are spent on this question, largely referring to
the work of Savage-Rumbaugh (1986) and the Yerkes
Primate group. We learn that a few well-trained and
human-family raised chimps have shown some symbol
use,
as
in limited learning
of
American Sign Lan
guage. At least two Bonobo (pigmy) chimps have
learned signed language implicitly by observing their
parents trained. Oddly, these young Bonobos use their
language more naturally and better than others who
have had much more explicit training. (Available vid
eotapes of the brightest and best animals show skills
more dramatic than even Deacon describes, as in one
chimp signing to another, totally using symbol-based
lexicon, that she would like different food or nonfood
objects to be given or used in specific ways.) Here,
the animal s behavior is based on the communication
of
shared rule-governed arbitrary logical categories
and their specific labels similar to humans between 2
and 3 years of age. Of course, there is a lot more to
a 3-year-old human s cognition--ehimps don t ask a
lot of why
questions-but
the most symbol-minded
chimps are still very impressive.
The point
is
that with the right setup and enough
preparation, some nonhuman primates can operate at
the symbolic, not just indexical conditioned-associa
tion level. Deacon believes that if he can find out just
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how chimps do it, he may have a clue to how humans
achieved symbolic functioning, which is our crucial
antecedent to rule-based grammatical language. This
discovery would obviate the need for positing an in
trinsic, built-in universal grammar module,
a
la Chom
sky, to explain the origin
of
human language. It is in
this discussion that Deacon reveals his antipathy for
a saltationist position, and his preference for a model
of gradualism and continuity in species evolution.
So what made the difference for humans? The
key to the discovery of symbol reference seems to be
a counterintuitive cognitive leap or trick. The very
same cognitive style, categorization by associative (in
dexical) learning, that defined successful adaptation
for many species for millions
of
years, had to be situa
tionally negated in order for higher logical categoriza
tion to occur at all. It works something like this: To
discover an abstract rule, you must apprehend that the
surface associations that define your reality must be
ignored, and then apprehend that a more abstract uni
fying principle exists that can categorize many objects
and events within an overarching system of logic. La
bels for indexical, practical living must always relate
back to the iconic re l world. But symbolic labels
can be anything you want, as long as they are members
of a family of commonly accepted concepts that give
meaning to each of the member labels or lexicon. So
an abstract, flexible rule must be grasped. It
is
very,
very hard for chimps to get a rule if an immediate
reward compels attention and action. Consider two
piles
of
candy, one large and one small. The pile you
piGk will be given to your competitor, the remaining
one is yours. It sounds easy: Pick the small one. But
small children and nonhuman primates, and patients
with certain PFC damage, repeatedly pick the large
pile, even though the rule has been demonstrated
many times. Now try this with an older child with a
healthy PFC or a chimp, both
of whom have learned
to respond to symbolic labels of pile size to help selec
tively suppress attention to the immediate token-object
associations. Voila We have logical rule-guided be
havior and delay of gratification, the step from which
the leap is taken to symbolic functioning.
As
Deacon
notes, [L]ike the chimps, hominids were forced to
learn a set of associations between signs and objects,
repeat them over and over, and eventually unlearn the
concrete association in favor of
a more abstract one.
What does this have to do with grammar-based lan
guage? Apply the new arbitrary rule-making capacity
to the subject and verb elements of your pragmatic,
holistic vocabulary, get everybody doing it, and you
have a symbolic language, even
if
rudimentary.
33
Later, Deacon shows how humans created vari
ous rituals that served to consolidate the symbol-sym
bol, symbol-real world links that made full language
possible. That in turn made group cohesion possible,
which made for social complexity pressures and re
sulting brain expansion. But Deacon's unique contri
bution to this literature, which he sprinkled throughout
the technical and philosophical chapters, in his discov
ery of the mechanisms of symbol discovery itself. His
theory answers, in a real way, all
of
his goals. It shows
how humans are special in our use of, and enslavement
by symbols, and why no other species came to do this
naturally. It also explains the adaptive problems that
were solved (and caused) by symbol use, putting hu
mans at the top
of
the food and technology chain.
Many important problems remain, however, and
Deacon is especially thorough in his explanation of
the brain-structure issue. Many primates have com
plex social group standards and the neurobiology to
support this. Why didn' t other species evolve the
structures for natural symbol discovery? Convergent
data generally have pointed to the PFC. And here is
one problematic area of the book: Deacon leans very
hard on the premise of an oversized human PFC to
account for human symbolization. But other careful
studies, by H Jerison (1997) and
H
Damasio's (Sem
endeferi, m s i o ~ Frank, nd Van Huesen, 1996)
group, seem convincing that the human PFC is about
the right volume for a primate with our bodies and
total brain size. Yet, the functions of the PFC, and
neuropathological studies, make it very tempting to
put the structural basis
of
symbolic function in the
PFC. In fact, shortly after Deacon's book was re
leased, a study by Stephen Wise,
E
A Murray, and
C
R Gerfon (1996) clearly demonstrated a PFC as
cending axis for abstract conditional responding,
which is present in many primates but most delineated
in humans. So Deacon's general emphasis on the PFC
is supported, but more work is needed to sort out the
functional specialization and connectivity versus ex
cessive volume controversy.
The study
of the particulars of human cognitive
evolution will always be
l ~ k i n
in physical evidence,
and will thus always be best understood as a choice
of
narratives. Who has the best story? It is common
to hear that we are the product of an interwoven causal
chain: extra-arboreal bipedalism, left hands freed for
tool making, gesturing, and accurate throwing, requir
ing a bigger brain. The bigger brain required an imma
ture birth, with greater sensitivity to postnatal
environment. This created pressures for social cohe
sion and problem solving, requiring complex language
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34
and culture and still larger brains. Deacon s narrative,
which denies none of the above, includes the notion
that bigger brains needed a meat diet and therefore
needed male provisioning and fidelity contracts (re
quiring rituals and delay of gratification symbols that
overcame immediate needs for philandering). This is
surely part
of
the story. I prefer a narrative that ad
dresses the early hominid s short, fear-dominated life.
Such a story would have early presymbols like safety
and danger signs becoming ritualized into anxiolytic
vehicles like superstition and special tokens and then
an animistic belief system with its own lexicon. I like
this because it seems earlier than the marriage con
tract. But who knows? No one can solve this puzzle,
so we look for cogent logic and the available physical
evidence for the best narrative. Deacon s emphasis is
strongest in its logic after some symbol capacity was
already present, because he can explain how symbol
mediated behavioral flexibility enabled hominids to
occupy niches that other animals could not. Our ances
tors therefore out competed and out survived and out
reproduced our competitors because
of
our behavioral
flexibility; symbolic reference is with us now because
it worked better than the extinct alternatives.
Havingdone the hardworkofmaking andbuilding
an extremely compelling case for the how and when of
symbolic reference, Deacon is now free to speculate
about what all this means. For example, he sees no rea
son why symbolizing creatures could not build sym
bolizing conscious artifacts, since reflective
consciousness is synonymous with the process
of
shar
ing symbols with oneself and others (empathy). Also,
Deaconbelieves that an algorithmfor constructing such
an artifact is close at hand. Others are less optimistic.
For example, Andy Clark
Being There: Putting Brain
Body and the World Together Again
1998) suggests
that human cognition, including symbols, is hopelessly
dependent on bodily states (including affect) and
wideware influences from an orchestrating environ
ment. This would mean that an artifact with disembod
ied cognition, no matter how smart, would be
forever handicapped in its consciousness
of
self and
others experience. But this remains to be seen.
Deacon also explores theextremesensitivity
of
the
newly expanded brain region, the PFC, that contributes
so much to symbolic reference. He notes that the very
PFC connections that make possible symbolic refer
encedo sobecause of recently evolved extraprojections
to this area, but without the reciprocal matching of
down flow regulation of limbic activation connections
from the PFC. This conflict between relative symbol
ization and overempowered emotionality makes us
Book
Reviews
constantly vulnerable to minor chemical variations and
pathological dysregulation, and accounts for currently
popular compounds like SSRls that facilitate PFC regu
latory functions. In other words, our symbolization is
clearly adaptive, but is unstable and very vulnerable to
runaway (obsessive), and blocking (alexythymia, anti
sociality) conditions that compromise effective symbol
use in a complex lifestyle.
Symbol use also makes us all extraordinary pos
sessors of virtual reality. Many animals have a kind
of contextual vicarious trial and error, but only hu
mans spin scenarios far from the field
of
action, plan
ning glorious, destructive and mostly mundane deeds.
Deacon understands that we are hopelessly enslaved
by this compulsion to find meaning in everything, for
better or worse.
Of course we think
of
ourselves as
far more than John McCrone s
The Ape that Spoke
(1991), but there is no guarantee that symbolization
will keep us special for very long. S
J
Gould (1993),
for example, reminds us that in geological time the
symbolic species is potentially just the fragile tip
of
a
twig on the evolutionary tree
of
life.
Deacon has clearly moved the scientific study of
symbolic reference and human intelligence several
steps forward. Has he done the same for understanding
language origins? Here is where the debate will con
tinue-happily because Deacon has added a fresh co
evolutionary approach-and because somany linguists
and psychologists are already committed to a position
as to
whether language is innately modular in the hu
man brain or not. Our group found Deacon s position
that language is nonmodular and nonintrinsic convinc
ing overall. We also liked his admitted personal at
traction to heresy and naturally rebellious nature
in investigating such an overheated subject. The re
viewer Robert Berwick gave Deacon a batting average
of
.400, based on Deacon s great explanation
of
the
brain but his failure to convince Berwick, a salta
tionist, that language developed continuously in the
environment and brain together. I guess we would give
Deacon a much higher batting average based on the
achievement of
his original goals.
When we finally ended our formal study
of
Dea
con s book (there will be no end to its influence on our
thinking about the evolution of brain and language) we
ran out
of
words to describe Deacon s remarkable
achievement. It was like facing an important problem
you never thought you would be able to solve and then
somehow thinking it through, close to transparency. Our
applied linguists thought Deacon s perspective on lan
guage
is
an important bridge in the debate, and our psy
choanalysts (who care more about how the mind works
7/25/2019 16 the Symbolic Species: The Co-Evolution of Language and the Brain
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or
doesn t
work) talked about neuroscience and their pa
tient care with a fresh and deeper awareness of brain be
havior relations. None
of
us, however, will ever think
the same way about what makes our species special.
References
Clark, 1998),
Being There: Putting Brain Body and
World Together Again. Cambridge, MA: MIT Press.
Gould, S J 1993), Full House. New York: Random House.
Jerison, H J 1997), Evolution of prefrontal cortex. In:
Development
of
Prefrontal Cortex Evolution Neurobiol-
ogy and Behavior. Baltimore, MD: Paul
H
Brookes.
McCrone,
J
1991), The p That Spoke: Language and
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