Kagan-2008-Child Development
Kagan-2008-Child Development
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delay, a large number of color photographs of unfamiliar objects for which they had no names, such as
telescope, toaster, and golf club. Both groups of children correctly recognized the pictures close to 90% of
the time (Kagan, Klein, Haith, & Morrison, 1973). It is
likely that the excellent memory performance of the
Mayan children was mediated by the schemata for
the pictures they acquired during familiarization.
Infants, like older children, create schematic concepts or prototypes that are averages of repeated
exposures to the same class of events. Eight-montholds have already acquired schematic concepts for the
acoustic envelopes of the vowels and consonant
vowel combinations of their language. However, they
lose the ability to distinguish between phonemes that
resemble the speech sounds they hear but do not
occur frequently (Doupe & Kuhl, 1999). The same
phenomenon occurs for schemata representing the
mouth movements of speakers (Weikum et al., 2007).
Infants can also create schematic concepts for temporal patterns of unfamiliar vocal sounds. Seven-montholds first heard a 2-min speech sample containing
three representations of each of 16, three-syllable
utterances of the form a-b-a, but the syllables in each
of the utterances were different. The only feature
shared by all the utterances was that the first and
third syllables were identical. After the infants were
familiarized with this pattern, they heard either an
utterance of the same forma-b-aor a new set of
three syllables with a new form; for example, a-b-b.
The infants were more attentive to the unfamiliar a-b-b
pattern, suggesting that they had created schematic
concepts for the temporal pattern of these meaningless
vocal sounds (Marcus, Vijayan, Rao, & Vishton, 1999).
An important distinction between schemata and
semantic structures is that only the latter imply both
the essential features a referent possesses and some
features it does not possess. This logic does not
apply to schemata. The sentence, The leaf is on the
ground, implies that there was a time in the past
when it was not on the ground; the schema of a leaf
on a lawn does not contain that extra knowledge.
A second distinction is that most of the time schemata can be transformed without any accompanying cognitive tension. Dreams and reveries provide
classic examples. The image of a smiling face can turn
into a pumpkin without any of the cognitive dissonance that would occur if a person read, A smiling
face is a pumpkin. Einsteins image of riding a light
wave is said to have been one of the origins of his
theory of special relativity. However, the printed
sentence, Humans can move at the speed of light
would evoke in most readers an immediate sense of
impossibility.
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to acknowledge the importance of the source of evidence, or are indifferent to the physical features of
the stimulus arrays. The three claims refer to young
infants possession of the concept of number, physical
impossibility, and permanent objects. The concept of
number is considered first. Some scientists attribute
to young infants a concept of number, as contrasted
with a perceptual representation of quantity because
they can distinguish between displays of different
numbers of dark circles in a habituation dishabituation design. However, Fantz and Fagan (1975) noted,
over 30 years ago, that young infants look longer at
a design with 20 squares than at one containing only 4
squares because of differences in the amount
of contour derived from a combination of the size of
each element and the number of elements.
Mix, Huttenlocher, and Levine (2002), who reviewed
the literature on the concept of number, concluded
that the infants ability to discriminate among different numbers of elements, as long as the numbers were
less than four or five, was based primarily on perceptual features, especially total area, size, and density of
the elements, and total contour length (see Tan &
Bryant, 2000, for a similar conclusion). When these
physical properties were controlled, 6-month-olds
behaved as if they could not discriminate between
one and two objects (Xu, Spelke, & Goddard, 2005).
These observations imply that the infants ability to
perceive differences in the size and density of elements and amount of contour is qualitatively different from the older childs symbolic concept of number
(see Feigenson, Carey, & Spelke, 2002). Indeed, in
some contexts, 12-month-olds behave as if they
can only create and hold in working memory perceptual representations for up to three objects (see
Ross-Sheehy, Oakes, & Luck, 2003). One-year-olds
who see an examiner place four crackers in a box do
not persevere in searching for additional crackers
after retrieving the first one, but will do so if they
see the examiner place only two crackers in the box,
implying that they regard any quantity of cracker
greater than three as belonging to a single, amorphous
category (Feigenson & Carey, 2005). Le Corre and
Carey (2007) suggest that the representation of the
cardinal numbers that children use when they count
is not an obvious derivative of the infants perceptual
representations of quantity.
My front lawn has eight trees, a fact I was unaware
of until moments ago when I counted them. But when
I gaze out the window in summer, I do not see a set of
eight objects, but an array of tall green-gray objects in
the context of a sloping, green lawn. Major changes
occur between the infants perceptual ability to discriminate between arrays of three and six circles and
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did not appear, but few scientists would claim that the
animals possessed a representation of the causal
relation between their actions and the delivery of
a few pellets. There is a great deal of evidence to
suggest that the first signs of the ability to infer the
invisible events that might mediate an outcome do
not emerge until the middle of the 2nd year (Kagan,
1981). Causality, as Hume understood, is a symbolic
invention and is not contained in a perceptual schema.
It is important to appreciate that 2-year-olds, who
have some language and an improved working
memory, do not infer the correct location of a ball that
rolls down an incline to strike a tall, clearly visible
occluder. In this study, the examiner placed the
occluder behind one of the four doors over a series
of trials and asked the child to guess which door
should be opened in order to retrieve the ball. Twoyear-olds could not solve this problem; that is,
they were unable to infer the correct door to open
from their perception of the location of the occluder
(Berthier, De Bois, Poirier, Novak, & Clifton, 2000).
However, 2-year-olds do show increased attention if
a puppet, who had been successfully retrieving a ball
from the correct door, failed to reach for the object at
the door representing the correct location (Mash,
Novak, Berthier, & Keen, 2006). Hood, Cole-Davies,
and Dias (2003) performed a similar experiment with
a similar result. Two-and-a-half-year-olds stared for
several seconds when a toy that had rolled down
a ramp and struck an occluder suddenly appeared
on the other side of the occludera physically impossible eventbut failed to search correctly for the toy
at the place where the occluder rested.
These results affirm the earlier suggestion that the
predicate know has two different meanings in these
varied experimental contexts. One refers to prolonged
attention following the violation of a perceptual expectation; the second refers to a conceptually richer
representation that includes an inference representing a necessary relation between the location of an
occluder and the location of an object. Because the
2-year-olds did not reach correctly for the object when
they could see where the occluder rested, investigators may be going beyond the evidence when they
conclude that infants less than 1 year know that
objects cannot pass through a solid barrier and imply
that know has the same meaning for infants that
it has for older children.
Object Permanence
Eight-month-olds administered the Piagetian A
not B task often stare briefly at the correct location
of a hidden object but reach incorrectly (Ahmed &
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and increased coherence between frontal and temporal occipital sites (Bell & Wolfe, 2007). The various
waveforms of the ERP also undergo a major change
between 3 and 24 months (Jing & Benasich, 2006;
Richards, 2003; Scott, 2006; Webb et al., 2005), and the
amplitudes of the P2/N2 waveform to click sounds
increase in a linear fashion between 1 and 12 months
(Ohlrich & Barnet, 1972). In addition, the proportion of
quiet sleep associated with sleep spindles (12 14 Hz)
increases in precentral sites at 9 10 months (Tanguay,
Ornitz, Kaplan, & Bozzo, 1975).
The brain continues to mature after the first birthday. Blood flow is greater to the right than to the left
hemisphere during the opening 3 years but shifts to
more predominant flow to the left hemisphere at
about 4 years of age (Chiron et al., 1997). Synaptic
density in the primary auditory cortex does not reach
adult values until puberty; dendrites on neurons of
the dentate nucleus of the cerebellum undergo intensive lengthening and extension, and the basal ganglia
continue to develop during the 2nd year. Dopamine
receptors in the caudate nucleus (especially D1 and
D2 receptors) do not reach maximal density until the
middle of the 2nd year and the neurons of Cortical
Layer 3, which comprise the cells of the corpus callosum,
increase in size during this interval (Huttenlocher &
Dabholkar, 1997).
The concentration of the enzyme involved in the
synthesis of acetylcholine increases sharply during
the 2nd year when pyramidal neurons begin to
express acetylcholinesterase in cell bodies and fibrillary networks (Black, 1991; Blokland, 1996). The
innervation of Layer 3 pyramidal neurons by acetylcholinesterase and the growth of Layer 3 neurons
probably contribute to the seminal advances of the
2nd year, especially the emergence of language,
a moral sense, and self-awareness (Kagan, 1981;
Mesulam & Geula, 1991). Finally, the human brain
does not attain 90% of its adult weight until 7 or 8
years of age (Giedd et al., 1999), the density of D1
receptors in the basal ganglia does not attain peak
density until 4 8 years (Seeman et al., 1987), the
degree of coherence of various EEG frequency bands
between frontal and occipital or temporal areas increases after the third birthday, and the latency to the
peak value of the N170 waveform to faces decreases
by as much as 10% between 5 and 7 years of age
(Taylor, McCarthy, Saliba, & Degiovanni, 1999).
In sum, between the first and the eighth birthdays,
the human brain attains peak synaptic density, maximal glucose uptake in the prefrontal cortex, peak
concentrations of dopamine and norepinephrine receptors, myelination of long cortical tracts, coherence
in the EEG, and maximal differentiation of dendrites
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Final Summary
The most enthusiastic advocates of a return to nativism do not insist that the infants concepts for number,
physical impossibility, causality, or the permanence of
objects are essentially the same as those of adolescents. The central suggestion in this article is that the
perceptual representations that comprise schemata
are to be distinguished from the conceptual structures
involving semantic forms and inferences about events
that were not experienced. Infants turn away from
dissonant musical chords but do not possess the
musicians concept of dissonance; infants who grasp
an object placed in their palm do not understand the
concept mine. Spelke (1994), an influential advocate and sophisticated experimental psychologist,
reminds us that there is no consensus as to when
particular knowledge structures appear, how they are
altered with growth and experience, what role the
infants representations play in the later development
of thought and reason, and adds, wisely, that the
infants cognitive functioning has to differ from that
of adults because distinct knowledge systems are
less interconnected during the 1st year of life
(Spelke, Vishton, & Von Hofsten, 1995, p. 177).
Hence, it is appropriate to ask why the notion that
young infants possess conceptual talents resembling
those of older children became attractive to a select
cohort of developmental psychologists in such
a short time. One speculative explanation is that
there is a competition for dominance between the
language networks of biology and those of the social
sciences. The dramatic advances in molecular biology and neuroscience, which are to be celebrated,
have led most biologists, but a smaller number of
social scientists, to assume that the vocabulary of the
brain sciences will prove to be more fruitful than the
psychological concepts that emerge from brain activity and depend on the products of experience. This
article has suggested that a construct purporting to
explain a psychological competence as a process
inherent in the infants brain organization need not
have the same meaning as one that explains a process
requiring extensive experience. However, some younger scientists have become attracted to the language
networks of biology and neuroscience because these
domains have become challenging areas of inquiry
that provide generous research funds to those who
study the relation between biological and psychological
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Kagan
similarity in mechanism between the cognitive functions of infants and older children. My skepticism
rests on the observation that it is rare, in any scientific
domain, for a single measure to reveal all that is
necessary to understand a phenomenon. Hence, it is
reasonable to question the assumption that an
increase in fixation time of a few seconds to an event
that violates an acquired perceptual expectation,
without any other evidence, is a sufficient basis for
inferring that infants under 6 months possess a conceptual representation of number, physical impossibility, causality, or the permanence of objects that
shares important features with the competences
awarded the same name in older children.
References
Ahmed, A., & Ruffman, T. (1998). Why do infants make A
not B errors in a search task, yet show memory for the
location of hidden objects in a nonsearch task? Developmental Psychology, 34, 441 453.
Almli, C. R., Rivkin, M. J., McKinstry, R. C., & the Brain
Development Cooperative Group. (2007). The NIH
MRI Study of normal brain development: Newborns,
infants, toddlers, and preschoolers. Neuroimage, 35,
308 325.
Arriaga, R. (2001). Behavioral and electrophysiological correlates of numerosity discrimination in eight-month-old infants.
Unpublished doctoral dissertation, Harvard University,
Cambridge, MA.
Aslin, R. N. (2000). Why take the cog out of infant
cognition? Infancy, 1, 463 470.
Aslin, R. N. (2007). Whats in a look? Developmental Science,
10, 48 53.
Baillargeon, R. (1994). How do infants learn about the
physical world? Current Directions in Psychological Science,
3, 133 140.
Baillargeon, R. (2000). Reply to Bogartz, Shinskey, and
Schilling; Schilling; and Cashon and Cohen. Infancy,
1, 447 462.
Bar, M., & Neta, M. (2007). Visual elements of subjective
preference modulate amygdala activation. Neuropsychologia, 45, 2191 2200.
Beeman, M., & Chiarello, C. (1998). Right hemisphere
language comprehension. Mahwah, NJ: Erlbaum.
Bell, M. A., & Wolfe, C. D. (2007). Changes in brain
functioning from infancy to early childhood. Developmental Neuropsychology, 31, 21 38.
Berthier, N. E., De Bois, S., Poirier, C. R., Novak, M. A., &
Clifton, R. K. (2000). Wheres the ball? Developmental
Psychology, 36, 394 401.
Black, I. B. (1991). Information and the brain. Cambridge,
MA: MIT Press.
Blokland, A. (1996). Acetylcholine: A neurotransmitter
for learning and memory. Brain Research Review, 21,
285 300.
1621
de Haan, M., & Nelson, C. A. (1999). Brain activity differentiates face and object processing in six-month-old
infants. Developmental Psychology, 35, 1113 1121.
Dehaene, S. (1997). The number sense. New York: Oxford
University Press.
Dehaene, S. (2007). A few steps toward a science of mental
life. Mind, Brain, and Education, 1, 28 47.
Deloche, G., Seron, X., Scius, G., & Segui, J. (1987). Right
hemisphere language processing. Brain and Language, 30,
197 205.
de Schonen, S., & Mathivet, E. (1990). Hemisphere asymmetry in a face discrimination task in infants. Child
Development, 61, 1192 1205.
Diamond, A. (1990). Developmental and neural bases of
memory functions as indexed by the AB and delayed
response tasks in human infants and infant monkeys. Annals of the New York Academy of Sciences, 608,
267 309.
Doupe, A. J., & Kuhl, P. K. (1999). Birdsong and human
speech. Annual Review of Neuroscience, 22, 567 631.
Ellis, H. (1900). The analysis of the sexual impulse. Alienist
and the Neurologist, 21, 247 262.
Fantz, R. L., & Fagan, J. F. (1975). Visual attention to size
and number of pattern details by term and pre-term
infants during the first six months. Child Development, 46,
3 18.
Feigenson, L., & Carey, S. (2005). On the limits of infants
quantification of small object arrays. Cognition, 97,
295 313.
Feigenson, L., Carey, S., & Spelke, E. (2002). Infants
discrimination of number vs. continuous extent. Cognitive Psychology, 44, 33 66.
Fenwick, K. D., & Morrongiello, D. A. (1998). Spatial colocation and infants learning of auditory-visual associations. Infant Behavior and Development, 21, 745 760.
Fiske, J. (1883). The meaning of infancy. Boston: HoughtonMifflin.
Fox, N., Kagan, J., & Weiskopf, S. (1979). The growth of
memory during infancy. Genetic Psychology Monographs,
99, 91 130.
Frick, M., & Colombo, J. (1996). Individual differences
in infant visual attention: Recognition of degraded
visual forms by four-month olds. Child Development,
67, 188 204.
Giedd, J. N., Blumenthal, J., Jeffries, N. O., Rajapakse, J. C.,
Vaituzis, A. C., & Liu, H. (1999). Development of the
human corpus callosum during childhood and adolescence: A longitudinal MRI study. Progress in Neuropsychopharmacology and Biological Psychiatry, 23, 571 588.
Hagler, D. J., Riecke, L., & Sereno, M. I. (2007). Parietal and
superior frontal visuospatial maps activated by pointing
and saccades. Neuroimage, 35, 1562 1577.
Haith, M. M. (1998). Who put the cog in infant cognition?
Infant Behavior and Development, 21, 167 179.
Haith, M. M., & Benson, J. B. (1998). Infant cognition.
In W. Damon (Series Ed.) &D. Kuhn & R. S. Siegler
(Vol. Eds.), Handbook of child psychology (Vol. 2, 5th ed.,
pp. 199 254). New York: Wiley.
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