CORTEX
D. Povinelli
and T. Preuss
- Evolution of theory
of mind
Theory of mind: evolutionary
cognitive specialization
history
of a
Daniel J. Povinelli and Todd M. Preuss
Traditional
analyses of the evolution
ity among
species. However,
particular
kind of intelligence
intentions
and beliefs. Data indicate
as those
of others,
might
Behavioral
studies
in children
in the developmental
patterns
in the same manner.
mind, forever
Trends
Neurosci.
altering
(1995)
I
that
be the
their
research
is related
result
TN.7 Vol. 18, No. 9, 1995
that
to reflect
of evolutionary
reveal
Humans
might
commonality
might
mental
have specialized
states
in the
both similarities
capacities.
a cognitive
in a
such as desires,
states, as well
prefrontal
and striking
Humans
but it is too early to be certain
have evolved
and continu-
on one’s own mental
changes
that lead to theory-of-mind
of social behavior,
humans
to understanding
that the ability
cortex.
differences
and great
apes
if they interpret
specialization
in theory
of
view of the social universe.
18, 418-424
N CULTURES around the world, humans exhibit an
automatic and pervasive folk psychology that interprets the behavior of the self and others in terms
of inferences about unobservable mental states such
as desires, intentions
and beliefs’. Premack and
Woodruff2 coined the term ‘theory of mind’ to refer to
this system of inferences, noting that an ability to represent and infer mental states from the self and others
‘may properly be viewed as a theory because such
states are not directly observable, and the system can
be used to make predictions about the behaviors of
others’. This folk psychology encapsulates much of
what it means to be human: our commitments to the
self and others as mental agents replete with emotions,
desires, beliefs, personalities and personal histories.
Are humans alone in this thoroughly mentalistic
interpretation of the self and others? Or did theory of
mind evolve before the emergence of humans? Surely
this is one of the most interesting and significant
questions that we can ask about the evolution of
human nature, yet it is one that has escaped empirical
attention until quite recently.
Daniel J. Povinelli
This review explores the hypothesis that theory of
is at the Laboratory
mind is a recent evolutionary innovation. A strong
of Comparative
version of this hypothesis is that the ability to
Behavioral Biology,
attribute mental states, together with the specific
New Iberia
neural organization that makes such attributions
Research Center,
possible, is a unique specialization of the human
New Iberia, LA
species. This would imply that theory of mind
70560, USA, and
emerged during the past several million years, after
the Dept of
the divergence of humans and apes. An alternative
Psychology, Tulane
hypothesis is that at least some aspects of theory of
University, New
mind were already in place before the emergence of
Orleans, LA, USA,
the human species, and might, therefore, be present to
and Todd M. Preuss some extent in other primates, and most likely the
is at the Dept of
great apes. Nonetheless, if this view is correct, it would
Psychology,
mean that although for hundreds of millions of years
Vanderbilt
animals have been operating on the basis of implicit
University,
‘intentions’ and ‘knowledge’ stored in their neural
Nashville, 7N
circuitry, it was not until relatively recently that evo37240, USA.
lution produced animals with brains capable of rep418
have emphasized
suggests
and chimpanzees
pathways
share many ancient
them
recent
of intelligence
resenting those mental concepts explicitly. In other
words, although many organisms routinely form
neural states instantiating desire, intention and belief,
it is possible that only a few species (and possibly only
humans) have the ability to reflect upon these states.
The evolution of a psychological system that is capable
of representing such mental states would not require a
precise understanding of the neural architecture that
encodes them. After all, even an approximation of the
workings of such mental states - a theory of mind might allow organisms to predict the behavior of their
conspecifics with considerable accuracy.
The purpose of this article is twofold. First, we establish a neural and psychological framework from which
to consider the evolution of theory of mind. Second,
we review the evidence that concerns the development of theory of mind in human children, and what
is known about its development (or lack thereof) in
great apes and other non-human
primates. This
review makes a preliminary assessment of alternative
hypotheses of the timing of the evolution of various
aspects of theory of mind and, in particular, the
hypothesis that theory of mind, at least in an elaborated form, is a psychological specialization of the
human species.
Human
brain
specialization
Figure 1 depicts the evolutionary relationships
among humans and our closest living relatives, the
great apes. Evolutionary
reconstructions
of the
features that were likely present in the common ancestor of great apes and humans suggest that each of its
living representatives has departed in important ways
from the ancestor, which was probably an arboreal
ape of about 30 kg (Ref. 3). Orang-utans, for example,
have become extreme arboreal specialists with important modifications that occur in the wrist, shoulder
and hip to allow for more extreme suspensory postures.
The African apes (chimpanzees and gorillas) have
developed specializations for a distinctive form of
terrestrial quadrupedalism called ‘knuckle-walking’, in
0 1995, Elsevier Science Ltd
D. Povinelli
which the weight of the upper body is borne on the
middle phalanges of the hands. Humans have departed in an even more bizarre manner from the
ancestor of the great-ape-human group, with a radical
remodeling of the pelvis and lower limb to support
habitual bipedalism4f5.
Just as in musculoskeletal structure, the brain too
has undergone dramatic evolution following the
divergence of the human lineage from that of the
African apes, -5-8 million years ago. The brain
increased in volume by approximately threefold, and
the fossil evidence indicates clearly that most of the
increase occurred during the past 2 million years, long
after the evolution of bipedality’. Not only did the
volume of the brain increase during human evolution
but there was also a disproportionate enlargement of
the association cortex, and especially the prefrontal
cortex, which occupies -24% of the cerebral mantle in
humans, compared with -14% in great apes6. The
expansion of the human prefrontal region might be
related to the evolution of specialized neural systems
that subserve distinctive human cognitive capacities’,
including theory of mind. In a number of theoretical
accounts, prefrontal cortex has been accorded a supervisory or executive role in the cognitive system, serving as the substrate by which mental representations
of the state of the world exert their influence on other
brain systems that control attention, memory and
action’-“. Moreover, what is regarded as the peculiarly
adaptive or flexible character of human behavior, and
the insightful,
self-reflective character of human
thinking, has been attributed to the action of frontallobe systems’. The ability to regulate behavior
through the use of representations of the mental states
of oneself and others might be a human specialization
of the representational
capacities present in the
prefrontal cortex of other primates (compare Ref. 9).
In fact, studies of autistic individuals suggest that
human theory-of-mind
capacities involve frontal
cortex. Autistic individuals show little understanding
of their own mental states, or those of others and, thus,
perform very poorly on formal theory-of-mind tasks,
relative to mental-age-matched
controls”. Autistics’
lack of insight and introspection is reminiscent of
deficits that result from frontal lesions, as is their
stereotyped, perseverative behavior, prompting the
suggestion that frontal-lobe dysfunction is an important element in autism’z-‘4. This view is supported
by a recent demonstration of activation in orbital prefrontal cortex during performance of a theory-of-mind
taskls.
If theory of mind is an evolutionary specialization
of human cognition, it should be expected that there
are corresponding
specializations at the level of
neural systems. Unfortunately, apart from the fact that
the human brain is unusually large, and the prefrontal
region disproportionately
so, very little is currently
known about how human cerebral organization differs from that of our closest relatives. Thus, our current understanding of possible human specialization
in theory of mind is based largely upon behavioral
studies. Developmental
psychologists have undertaken substantial research to characterize the development of theory of mind in children. Likewise, comparative psychologists are beginning
to explore
whether other non-human primates possess a similar
‘folk psychology’.
and T. Preuss
- Evolution of theory
CORTEX
of mind
Fig. 1. The great apes and humans share a common ancestor approximately 12-15
million years ago. Although the exact relationships among gorillas, chimpanzees and
humans are still uncertain, it is wide/y acknowledged that the other living great ape, the
orangutan, diverged considerably earlier.
Theory
of mind
in humans
and other
primates
Knowledge and belief
Large portions of the adult human theory of mind
are established firmly in children between three
and five years of age16-18.Perhaps the quintessential
achievement of the four- to five-year-old is the clear
understanding that beliefs are mental representations
- internal states that are formed as people interact
with the world. The standard test of thii achievement
involves determining at what age children understand
that the mind can represent incorrectly a true state of
affairs in the world; in other words, when they understand the notion of false belief”. Understanding that
beliefs can be false is an excellent diagnostic of theory
of mind because, in this case, an organism must keep
track of the divergence between the mind and the
world, thus demonstrating clearly that it understands
the distinction between the two. Research on children’s understanding
of false belief suggests that
between three and five years children solidify their
understanding of the mind as a mechanism that creates mental representations (and misrepresentations)
of the external world”.
Four-year-olds also understand some of the ways in
which belief and knowledge states arise. For example,
they understand that perceptual contact with a situation or event is a sufficient (and in some cases necessary) condition for one to possess a privileged state of
knowledge as compared with someone who has not
had similar perceptual contact. In the case of visual
perception, a four-year-old who observes someone
peering into a box automatically attributes to that person knowledge of the box’s contents; likewise they
attribute ignorance to someone who merely touches
the box”. Strikingly, younger children appear unaware of this crucial aspect of acquisition of knowledge, failing to grasp that the person who did not look
into the box has no way of knowing what was inside.
Indeed, young three-year-olds apparently do not even
know how they themselves come to know certain
TINS Vol. 18, No. 9, 1995
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D. Povinelli
and T. Preuss
- Evolution of theory
of mind
Povinelli and his co11eagues25,26,
has explored what (if anything)
chimpanzees understand about the
connection between seeing and
knowing. For example, in the procedure shown in Fig. 2, if chimpanzees understand the seeingknowing relationship, they ought
to choose the ‘advice’ offered by the
trainer who hid the food (or the
person who was carefully watching
while it was being hidden), as opposed to someone else who could
not see the hiding event. In general,
these tasks have yet to produce
definitive
evidence that chimpanzees, or other non-human
primates, such as macaques27,28,
understand the perception-knowledge relationship. Finally, there are
a number of observational reports
of apparent deception in nonhuman primates (especially chimpanzees”), and it is tempting to
interpret them as evidence that
non-human
primates understand
that other agents have beliefs that
can be manipulated. Very little experimental work has investigated
non-human primates’ understanding of false belief 24.However, if these
animals do not understand how
beliefs arise (as the experimental
data suggest), it seems unlikely that
they could make the distinction
between true and false beliefs.
Emotions and desires
The four-year-old’s discovery that
mental states such as belief are
internal representations
of the
external world clearly unites their
emerging theory of mind with our
Fig. 2. By the age of four years, young children understand how the act of seeing creates internal knowlown. However, children younger
edge states but it is not clear if chimpanzees ever understand this relation. The experimental
procedure
that
than four years might already underis used to investigate
chimpanzees’
and children’s
understanding
of the perception-knowledge
re/ationshipz6:
stand other, nonrepresentational
a chimpanzee
watches
as one experimenter
(guesser; A) leaves the room and a second experimenter
(knower;
B) hides food under one of several cups. (C) Both experimenters
later point to different
cups. (D) Transfer promental states, and they might even
cedure in which logical epistemoiogical
relationships
between seeing and knowing
are held constant
but the envipossessa nonrepresentational underronmental
variables
that define the role of the knower and guesser are altered. With sufficient
experience,
chimstanding of belieP0j31.Two-year-olds
panzees can learn to form a discrimination
between the two roles but, in their initial tria/s, they choose random/y.
talk extensively about certain mental
These findings raise the possibility
that they solve the task by relying on learned behavioral
strategies
(for examstates, such as emotions and desires,
ple, ‘pick the person who stayed in the room’),
rather
than on mentalistic
inferences
about the connection
that
are not representations of the
between seeing and knowing.
By contrast,
when this same nonverbal
task is administered
to four-year-old
chilexternal
world but are nonetheless
dren, most choose the correct person from the first trial forward;
three-year-olds
respond random/y23.
thoroughly
mentalistic concepts.
For example, the subtle ways in
facts (did you see what was in the box or did I tell which young children use mental verbs such as ‘want’,
you?), even in cases where their knowledge was ‘hope’, and ‘wish’, suggest strongly that they know that
they, along with others, are ‘repositories’ of unobservable
acquired just seconds earlier21-23.This is not to say that
three-year-olds lack the concept of knowledge alto- mental states, even if they have not yet grasped how the
gether; they might possess an earlier understanding of mind can also serve as a mechanism to copy or represent
knowledge, perhaps one in which knowledge is con- the state of affairs in the world3’. Furthermore, experimental research has revealed consistently and conflated with desire (T.D. Lyon, PhD Thesis, Stanford
University, 1993).
vincingly that three-year-olds understand that people
Do non-human primates represent the beliefs of act on the basis of their desires, that they distinguish
others? To date, most research on non-human pri- between someone thinking about something compared
mates’ understanding
of belief has focused on with someone having it, and when someone’s beliefs
whether they understand the perceptual basis of are stipulated they can even make correct predictions
acquisition of knowledge. Premackz4, as well as about how that person will behave”. In general,
420
TINS vol. 18, NO. 9, 1995
D. Povinelli
and T. Preurs
- Evolution of theory
CORTEX
of mind
Fig. 3. Chimpanzees
and orang-utans
(but not other primates)
show clear evidence of recognizing themselves in mirrors. Like most
animals, chimpanzees react initially to mirrors as if confronted by another member of their species, and typically engage in a variety of
social behaviors. However, in as little as S-30 min, many chimpanzees begin to engage in self-exploratory behaviors in which they use
the mirror to gain access to previously unavailable information about their appearance. They use mirrors to make exaggerated facial displays (A and B), as we// as groom their body, face and teeth (C-F). Many of the chimpanzees that display the types of se/f-exploratory
behaviors that are shown in C-F also will use a mirror to locate and inspect red marks p/aced surreptitiously on their ears and eyebrow
ridge47s49,50.
Organisms such as Old World monkeys, which do not display these spontaneous episodes of using the mirrors to explore their
bodies, also fail to explore marks that were placed on their face by experimenters4648.
younger children’s relative ease in understanding
desires, as opposed to thoughts and beliefs, has led a
number of researchers to propose the existence of a
specific developmental pathway in which children come
to grasp nonrepresentational
aspects of the mind
before understanding
the representational aspects,
such as those tapped in false belief and knowledgeattribution tasks31,33.
Given that children have a better understanding of
desires before beliefs, it is reasonable to ask if chimpanzees or other non-human primates display a better
understanding
of desires than they do of beliefs.
Premack and Woodruff’s2 original investigation of
theory of mind tested whether a chimpanzee could
attribute desires or goals to actors who were struggling
to solve staged problems. After observing videotapes
of these problems, the chimpanzee correctly selected
photographs that depicted solutions to the actors’
implicit desires or goals, as opposed to those that
depicted associated events. In a different study,
Povinelli and his colleagues trained chimpanzees to
co-operate with a human partner on a task that
required each to perform a different action (role), in
order to achieve a common goa134.The crucial finding
TINS vol. 18,No.9,
1995
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D. Povinelli
and T. Preuss
- Evolution
of theory
of mind
Fig. 4. Humans and chimpanzees
share portions
of the developmental
pathway
that controls
the expression
of gaze-following.
By 18 months, human
infants are capable of responding to the shift in orientation of the gaze or head posture, or both, of another by following their line of sight, including tracking
this line into the space behind them 43. One possible interpretation of this type of behavior is that it reflects a type of ‘joint-visual attention’ in which the infant
and adult appreciate the attentional focus of each other. That is, not on/y do they have a mechanism that serves joint attention43, they might also appreciate
that they share the same subjective attentional experience44. (A-C) Research with chimpanzees reveals that they a/so display this phenomenon [as, indeed,
might other social mammals) 57. However, additional research with chimpanzees (see Fig, 5) indicates that they might not represent the subjective attentional
state of the other oneJ6. This raises the possibility of both a developmental and evolutionary dissociation between joint-visual attention and the presence of a
folk psychological interpretation of visual perception as the mental state of attention.
There might even be earlier manifestations
of
human infants’ developing awareness of the subjective side of behavior. In the period leading up to
18-24 months, children begin to develop sophisticated behaviors that suggest at least an implicit awareness of the mental state of attention in themselves
and others. For example, proto-declarative pointing
(in which infants point to objects or events solely to
Early-emerging
knowledge
of se/f and others
draw the other’s attention to them) is consolidated by
In humans, the emergence of conceptual knowlabout 12 months4’, and between 12 and 18 months
edge of the self and others manifests itself at around
infants develop the ability to track another person’s
18-24months
in the transitional period between
line of sight into space outside of their own immediinfancy and early childhood. Indeed, this period
ate perceptual field 43. Some researchers have suggested
introduces such dramatic achievements by the child that these ‘joint-attention’
behaviors reflect44, or at
(not all limited to an understanding of mental states) least lay the perceptual foundations for45, an initial
that it is tempting to speculate (as did Piaget) that a understanding of the subjective attentional states of
fundamentally new conceptual system is emerging.
both the self and others. In an ingenious series of
Although even the very young infant has access to studies, Dare Baldwin and her colleagues have provided
proprioceptive
and kinesthetic information
that
evidence that, by at least 18 months, infants underenables it to distinguish self from the environment
stand that when another person looks or points at an
(self-perception), evidence for an objective underobject or event, that person becomes connected to it
standing of the self does not begin to emerge clearly subjectively through the mental state of attention4’j.
until -1Smonths. At this point, children recognize
Do non-human primates share even these limited
themselves in mirrors, engage in symbolic play, exhib- glimpses into the mind? Like humans, many chimit simple acts of altruism, participate in reciprocal co- panzees and orang-utans display clear evidence of recoperative actions with others, produce linguistic com- ognizing themselves in mirrors, whereas no other
ments about the failure of self-generated plans, display non-human primates have done so, despite extensive
mastery smiles upon completion of a task, and use research47,48(Fig. 3). The ability of these apes to recogmental state terminology that refers to desires32,36-41. nize themselves in mirrors has been replicated many
Each of these behaviors suggests at least a limited
times, and there is little doubt that they display the
understanding of the self and other as possessing same phenomenon of self-recognition as do 18-24agency, desires or internal emotional states, or both.
month-old children49,50. Gallup’s initial discovery of
was that the chimpanzees were able to reverse roles
immediately, assuming their partner’s role without
explicit training. In contrast, rhesus monkeys failed the
same role-reversal task3’. Collectively, these data suggest
that chimpanzees might possess some understanding
of goals or desires, although both of these studies have
enough methodological limitations to warrant further
research before firm conclusions are drawn.
422
TINS vol.
18, No. p. 1995
D. Povinelli
and T. Preuss
- Evolution of theory
CORTEX
of mind
Fig. 5. Although young chimpanzees are very sensitive to the eyes of others, they do not appear to understand them as ‘portals’ through which the mental
state of attention emanates. (A and B) Chimpanzees can be trained to use their natural begging gesture to request food from an experimenter. If an experimenter
stands on the left (A and B), the chimpanzee will gesture through the hole on the left side of the partition; if she stands on the right, the subject will gesture
there. However, this is no guarantee that the subjects realize that this person is subjective/y linked to them via the mental state of attention.
(C) When two
experimenters are used, one who can see the chimpanzees and one who cannot, the chimpanzees typically respond randomly j6 . They apparently fail to understand lhat on/y one of the experimenters is connected lo them through the mental state of attention, perhaps because they simply cannot represent such states.
Alternatively, they might simply fail to understand the specific role that eyes play in deploying attention. Young children that are tested similarly reveal an understanding of the subjective aspects of visual attention by about two and a half years of agej6.
self-recognition in chimpanzees led him to speculate
that chimpanzees might possess a self-concept.
Adopting a long-standing epistemological argument,
he further hypothesized that perhaps their knowledge
of self might enable them to make inferences about
such mental states as desires and beliefs in other?.
Thus, he has speculated that in organisms that are
capable of self-recognition, there might be a causal
connection between the onset of self-recognition and
theory of mind, with the critical factor being selfawareness51~s2.Consistent with his predictions, some
research has revealed correlations between the onset
of self-recognition in infants and their capacity for
altruism and the emergence of the self-conscious
emotions53*54. By contrast, Gallup’s proposal would be
in jeopardy if proto-declarative pointing and other
joint-attention
behaviors reflect a genuine understanding of the mental state of attention because, in
humans, joint-attention
behaviors typically emerge
by 12 months or so, long before self-recognition in
mirrors (18-24 months). At present, the paucity of
research in this area (especially with non-human
primates) makes a full evaluation of the proposition
difficult”.
Finally, there are some recent findings that concern
joint attention in chimpanzees, and that highlight
additional similarities and differences between humans
and chimpanzees. On the one hand, chimpanzees do
not naturally point to inform others about objects or
events, nor is it clear that training them to point, or to
respond to human pointing (see Fig. 2), produces an
appreciation of pointing as a way of co-ordinating the
mental states of self and others. On the other hand,
chimpanzees do display gaze-following abilities that
are as sophisticated as those of 18-month-old children56,57 (see Fig. 4). Although such gaze-following
abilities suggest that chimpanzees might appreciate
how the eyes connect someone’s internal states of
attention to the world (as do children by 18-24
months), a recent extensive investigation of this question has indicated that they do nots6 (see Fig. 5). These
somewhat contradictory findings raise a number of
possibilities. On the one hand, it might be that limited aspects of theory of mind were present in the
common ancestor of the great apes and humans, and
this is reflected in chimpanzees’ limited joint-attention
behaviors. On the other hand, these joint-attention
behaviors might have evolved for other reasons, and
might be controlled by psychological mechanisms
that evolved before a human specialization in theory
of mind (see Fig. 4), although in humans they now
function in concert with each other.
Reconstructing
the evolution
of theory
of mind
On the surface, much of the social behavior of the
great apes resembles our own so closely that it is
tempting to conclude that this behavioral similarity
must reflect similarity in subjective experience”. But
as developmental
and comparative psychological
research suggest, important
differences in how
humans, great apes and other animals interpret other
organisms might lie behind these behavioral similarities”. It is too early to be certain, but current evidence
does not yet exclude the possibility that, at some
point during human evolution, elements of a new
psychology were incorporated into existing neural systems - a psychology which, by its very nature, imbues
ancient behavioral patterns that we share with apes
with meanings they did not possess originally.
Selected
references
1 Povinelli,
D.J. and Godfrey,
L.R. (1993) in Evolutionary
Ethics
(Nitecki,
M. and Nitecki,
D., eds), pp. 277-324,
SUNY Press
2 Premack,
D. and Woodruff,
G. (1978) Behav. Bruin Sci. 1,515-526
3 Harrison,
T. (1991) in Or&e(s)
de la bipMie chez les hominides
(Coppens,
Y. and Senut, B., eds), pp. 235-244,
Editions du CNRS
4 Aiello,
L. and Dean, C. (1990) Human Evolutionary
Anatomy,
Academic
Press
T~S vol. 18, No. 9,199s
423
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D. Povinelli
Acknowledgements
Supported by
National Institutes
of Health Grant
No. RR-03583-05
to the USL-New
Iberia Research
Center, and
National Science
Foundation Young
Investigator Award
SBR-8458111
to
DIP. Photographs
by Donna T.
Bierschwule.
5 McHenry,
H.M. (1994) Proc. Nat1 Acad. Sci. USA 91, 6780-6786
6 Blinkov,
S.M. and Glezer, 1.1. (1968) The Human Brain in Figures
and Tables, Basic Books
7 Preuss, T.M. (1995) in The Cognitive Neurosciences
(Gazzaniga,
M.S., ed.), pp. 1227-1241,
MIT Press
8 Stuss, D.T. and Benson,
D.F. (1986) The Frontal Lobes, Raven
Press
9 Goldman-Rakic,
P.S. (1987)
in Handbook
of Physiology:
The
Nervous System, Vol. 5 (Mountcastle,
V.B., Plum, F. and Geiger,
S.R., eds), pp. 373-417,
American
Physiological
Society
10 Shallice,
T. (1988) From Neuropsychology
To Men&I Structure,
Cambridge
University
Press
11 Baron-Cohen,
S., Leslie, A. and Frith, U. (1985) Cognition 21,
37-46
12 Frlth, U., Morton,
J. and Leslie, A.M. (1991) Trends Neurosci.
14,433-438
13 Rogers, S.J. and Pennington,
B.F. (1991) Dev. Psychopathol.
3,
137-162
14 Brothers,
L. (1995) in The Cognitive Neurosciences
(Gazzaniga,
M.S., ed.), pp. 1107-1115,
MIT Press
15 Baron-Cohen,
S. et al. (1994) Br. 1. Psychiatry
165, 640-649
16 Flavell, J.H. (1988) in Developing
Theories of Mind (Astington,
J.W., Harris, P.L. and Olson, D.R., eds), pp. 244-267,
Cambridge
University
Press
17 Wellman,
H.M. (1990) The Child’s Theory of Mind, Bradford
Books
18 Pemer, J. (1991) Understanding
the Representational
Mind, MIT
Press
19 Wimmer,
H. and Pemer, J. (1983) Cognition 13, 103-128
20 Wimmer,
H., Hogrefe,
G-J. and Pemer, J. (1988) Child Dev. 59,
386-396
21 Gopnik,
A. and Graf, P. (1988) Child Dev. 59, 1366-1371
22 O’Neill,
D.K. and Gopnik,
A. (1991) Dev. Psychol. 27, 390-397
23 Povinelli,
D.J. and de Blois, S. (1992) 1. Comp. Psychol. 106,
228-238
24 Premack,
D. (1988) in Machiavellian
Intelligence (Byrne, R. and
Whiten,
A., eds), pp. 160-179,
Oxford University
Press
25 Povinelli,
D.J., Nelson,
K.E. and Boysen,
S.T. (1990) 1. Comp.
Psychol. 104, 203-210
26 Povinelli,
D.J., Rulf, A.B. and Bierschwale,
D.T. (1994)
I. Camp. Psychol. 108, 74-80
27 Cheney,
D.L. and Seyfarth,
R.M. (1990)
Anim. Behav. 40,
742-753
28 Povinelli,
D.J., Parks, K.A. and Novak,
M.A. (1991) I. Comp.
Psycho!. 105, 318-325
29 de Waal, F.B.M. (1982) Chimpanzee
Politics, Harper and Row
30 Harris, P.L. et al. (1989) Cognition Emotion 3, 379-400
and T. Preuss - Evolution of theoty
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40 Gopnik,
A. (1982) 1. Child Lang. 9, 303-318
41 Kagan, J. (1981) The Second Year: TheEmergence
ofSe@wareness,
Harvard University
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42 Bates, E. et al. (1979) in The Emergence of Symbols: Cognition and
Communication
in Infancy (Bates, E., ed.), pp. 69-140, Academic
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43 Butterworth,
G. and Jarrett,
N. (1991) Br. 1. Dev. Psychol. 9,
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44 Baron-Cohen,
S. (1994) Cum. Psychol. Cognition 13, 513-552
45 Hobson,
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Autism
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46 Baldwin,
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in Children’s
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of Mind (Lewis, C. and Mitchell,
P., eds), pp.
133-156,
Erlbaum
47 Gallup,
G.G., Jr (1970) Science 167, 86-87
48 Gallup,
G.G., Jr (1991) in The Self: an Interdisciplinary
Approach
(Goethals,
G.R. and Strauss, J., eds), pp. 121-135,
Springer-Verlag
49 Povinelli,
D.J. et al. (1993) I. Comp. Psychol. 107, 347-372
50 Gallup,
G.G., Jr et al. Anim. Behav. (in press)
51 Gallup,
G.G., Jr (1982) Am. I. Primatol. 2, 237-248
52 Gallup,
G.G., Jr and Suarez,
S.D. (1986)
in Psychological
Perspectives on the Self (Suls, J. and Greenwald,
A.G., eds), pp.
3-26, Erlbaum
53 Lewis, M. et al. (1989) Child Dev. 60, 146-156
54 Johnson,
D.B. (1982) Merrill-Palmer
Q. 28, 379-388
55 Povlnelli,
D.J. (1993) Am. Psychol. 48, 493-509
56 Povinelli,
D.J. and Eddy, TJ. Monogr. Sot. Res. Child Dev. (in
press)
57 Povinelli,
D.J. and Eddy, TJ. Psychol. Sci. (in press)
58 Tomasello,
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Book Reviews
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31 Wellman,
H.M. and Bartsch,
K. (1988) Cognition 30, 239-277
32 Bartsch,
K. and Wellman,
H. (1995) Children Talk About the
Mind, Oxford University
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33 Harris,
P.L. in Theories of Theories of Mind (Carruthers,
P. and
Smith, P.K., eds), Cambridge
University
Press (in press)
34 Povinelli,
D.J., Nelson,
K.E. and Boysen,
S.T. (1992) Anim.
Behav. 43, 633-640
35 Povinelli,
D.J., Parks,
K.A. and Novak,
M.A. (1992) Anim.
Behav. 44, 269-281
36 Amsterdam,
B. (1972) Dev. Psychobiol.
5, 297-305
37 Leslie, A.M. (1987) Psychol. Rev. 94, 412-426
38 Zahn-Waxler,
C. and Radke-Yarrow,
M. (1982)
in The
Development
of Prosocial
Behavior
(Eisenberg,
N., ed.), pp.
109-137,
Academic
Press
39 Brownell,
C.A. and Carrlger,
M.S. (1990)
Child Dev. 61,
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