When Less Is More: Poor Discrimination But Good Colour Memory in Autism
When Less Is More: Poor Discrimination But Good Colour Memory in Autism
When Less Is More: Poor Discrimination But Good Colour Memory in Autism
memory in Autism
Correspondence to:
UK.
Telephone: 020-7919-7884
Email: [email protected]
Abstract: In two experiments children with autism and two groups of controls
matched for either chronological or non-verbal mental age were tested on tasks of
significantly higher level than either group of controls. The findings suggest that
Introduction
unusually fine pitch discrimination has been noted in several experimental studies
(Bonnel, 2003; Heaton, Hermelin & Pring, 1998; Heaton, Pring & Hermelin, 1999;
Heaton, 2003; 2005) and this has lent support to models positing enhanced perceptual
functioning (Mottron & Burack, 2001: Mottron, Dawson, Soulières, Hubert &
Burack, 2006) or a bias to process and encode local information (Frith, 1989; Happé,
1999) in autism. The studies presented here will extend previous findings of enhanced
An aspect of autism that is likely to have significant implications for perceptual and
current theoretical accounts, relates to the delayed onset and wide variation in
shared features in visual arrays (Plaisted, 2001). But recent studies of face processing
in autism (e.g. Deruelle, Ronda, Gepner & Tardif, 2004) show that autistic individuals
may use substantially different attentional and processing strategies from typically
developing children, at least for visual tasks. Moreover, recent investigations into
perceptual categorization (e.g. Roberson, Davidoff, Davies & Shapiro, 2004, 2005:
Pilling, Wiggett, Özgen & Davies, 2003; Goldstone, 1998) show that language plays a
categorization. Findings from the developmental literature show that young children’s
knowledge of object names results in preferential looking at both objects (Baldwin &
Markman, 1989) and pictures of objects (Schafer, Plunket & Harris, 1999). Further,
exhaustive sorting of objects into groups occurs within a week of entering the
Since Brown and Lenneberg (1954) first proposed a direct relationship between
naming and memory for colors, many studies have supported the proposal that
coloured stimuli are coded both perceptually and verbally by adults (Kay & Kempton,
1984; Lucy, 1992; Alvarado & Jameson, 2005; Özgen, 2004; Gilbert, Regier, Kay &
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Ivry, 2005; Pilling, Wiggett, Özgen & Davies, 2003; Roberson & Davidoff, 2000;
Witthoft et al., 2003). Studies of typically developing children’s colour naming and
memory have shown that discrimination and memory for colours is facilitated by
knowing the appropriate label for a colour, relative to colours they cannot name
(Sandhoffer & Smith, 2001; Kowalski & Zimiles, 2006; Braisby & Dockrell, 1999),
and this is true even when children know only one or two terms (Roberson, Davidoff,
Davies & Shapiro, 2004). This evidence suggests that language plays an important
with and without verbal labels. As intelligence test score means for two of the
participants groups (Autism, MLD) were significantly below population norms, a pre-
test explored the extent to which each population could comprehend colour terms.
GENERAL METHOD
Participants
Thirteen children and adolescents with autism were recruited from a specialist school,
to which entry is dependent upon meeting criteria for autism outlined in DSM 1-V
(APA, 1994) or ICD-10 (World Health Organization, 1993). Testing using the Raven’s
Matrices task (Raven, Court, & Raven, 1992), a test of fluid intelligence, confirmed
that for the autism group, standardised scores were within the handicapped range.
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Measures of receptive vocabulary, using the British Picture Vocabulary Scales (BPVS;
Dunn, Whetton & Pintilie, 1997) were consistent with a group mean verbal mental
age (VMA) of 5 years. This profile, with non-verbal intelligence scores in the
moderate to mild range of handicap, and a large discrepancy between verbal mental
age (VMA) and chronological age (CA) is commonly associated with low-functioning
autism (LFA). There were two groups of control participants. The first were
were individually matched to the participants with autism for chronological age
(Typically Developing group) (TD). The second group of controls were recruited from
a school for pupils with Moderate Learning Disabilities (MLD) and were matched to
the children with autism for chronological age and non-verbal IQ. Age and
Comparison of the psychometric data for the autism and two control groups revealed
32.24, p<.001) and on verbal mental age measures (F (2,36) = 17.31, p<.001). Post-
hoc Bonferroni tests showed that TD controls had significantly higher Ravens
Matrices scores than MLD controls and participants with autism (both p<.05). Ravens
Matrices scores for MLD controls and participants with autism did not differ
significantly. TD participants had higher Verbal Mental Age scores than MLD
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controls and participants with autism (both p<.05), and MLD controls had higher
Verbal Mental Age scores than participants with autism (p<.05). Thus whilst
participants with autism were chronological age matched to both groups of controls,
and were also matched to MLD controls for non-verbal IQ, their language scores
(receptive vocabulary) were significantly poorer than those of both control groups.
11 colour tiles (prototypical examples of red, blue, yellow, orange, brown, pink,
purple, grey, black and white) were laid out on a table under natural daylight
conditions by a window. The experimenter read out the colour names, one at a time, in
random order and children were asked to point to the corresponding tile. Responses
A one-way Anova, carried out on the data failed to reveal a significant difference
Colours used in the following studies were glossy Munsell chips (Munsell, 1966).
Only the hue value of the colours varied, and chroma (colourfulness) and value
(lightness) were kept constant at Munsell levels 6/6. Good examples of the four
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primary hues (red, blue, green and yellow) at each of three hue levels were chosen
from the Munsell book and converted for the computer into L*u*v* co-ordinates
using Munsell conversion software. A full list of stimuli used in all three experiments
can be found in Appendix I. The selected coordinates were programmed into bit
images using CSS software and the stimuli were presented using e-prime software.
A portable spot chroma-meter was used to ensure that colours remained constant
Training trials: In eight trials (two for each of the four colours) participants saw
three colour patches, two of which (distractor patches) differed from the third (target
patches) in Munsell hue intervals of 8.5 or 9 steps (e.g. target = 1R6/6, distractors =
9.5R6/6 and 10R6/6). Thus the two distractors were always very similar to each other
and quite dissimilar from the target patch. Participants were instructed to point to the
most different patch (target) over as many trials as necessary to reach ceiling
Experimental trials: There were six trials of each colour (red, blue, green and
yellow) with the target stimuli differing from the two comparison stimuli by 1, 2 or
three Munsell steps. Each target appeared twice with each pair of distractors, making
Results.
The means and standard deviations for discrimination scores are shown in table 3.
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A 2-tailed binomial test showed that the means for the (lowest scoring) autism group
between group effect (F(2,36) = 7.86, p<.001). Post-hoc Bonferroni tests showed that
TD control scores were significantly higher than scores for MLD controls and
participants with autism (both, p<.05). There was no significant difference between
Within group correlations were carried out on the discrimination scores, the
chronological and verbal mental age scores and the non-verbal IQ scores. Of these,
only the discrimination and verbal mental age correlations for the autism group (r = .
shown one of four animal pictures (taken from Snodgrass & Vanderwart, 1980),
paired with one of four different prototypical colour patches (red, green, blue or
yellow). The four animal-colour pairings (e.g. dog paired with red, cat paired with
blue, pig paired with green and rabbit paired with yellow) were shown four times
each, making a total of sixteen familiarisation trials. In the test phase the previously
exposed animals (dog, cat, pig and rabbit) were shown individually together with all
four of the colour patches (red, green, blue and yellow). Participants were instructed
to select, by pointing, the colour that had been associated with the animal in the
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familiarisation trials. Each participant had four attempts to match each animal/colour
(16 in all). Order of presentation of the trials was randomised. Responses were
After a short break, the same familiarisation procedure was repeated for the second
phase of the experiment. However, in the test trials for phase 2, the pre-exposed
animals, were presented with three colour patches from the same colour category as
the patch paired with that animal in familiarisation trials (e.g. cat with three different
shades of blue). The position of the pre-exposed and distractor patches was
were again asked to point to the colour patch that had been paired with the animal in
Results
Table 4 shows the means and standard deviations from phase 1 and phase 2 of
experiment 2.
was 25%. In phase 2 there were 3 response options with a probability of chance
performance of 33%. To allow for differences in chance value scores, raw data were
converted into z scores. Z scores for the two phases of experiment 2 are shown in
table 5.
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As table 5 shows, all groups scored significantly above chance on phase 1. For phase
group variable and Condition (phase 1/phase 2) as the within group variable was
carried out on the data. This failed to reveal a significant main effect of Group (F
(2,36) = 2.71, p>.05). However, there was a significant main effect of Condition (F
Correlates of verbal labelling: Although the participants with autism knew colour
terms (naming pre-test), and their colour discrimination (experiment 1) was not
significantly different to that of controls matched for age and non-verbal intelligence,
their performance on experiment 2 suggested that they relied less on verbal labels and
variables are associated with information encoding strategies, memory scores (phase 1
& phase 2) were correlated with chronological age, verbal mental age, non-verbal IQ
11
and discrimination ability (scores for experiment 1) for the whole subject sample (n=
39). Scores for phase 1 (where targets could be correctly identified by verbal coding
only) correlated with VMA (r=.58, p<.001) and discrimination ability (r = .54, p<.01).
there was a significant negative correlation with VMA (r = -.36, p<.05). No other
correlations reached significance. Within group correlations carried out on the control
group data (MLD & TD) all failed to reach significance, so the data were then pooled
and the correlations were repeated. These showed that for these participants without
autism, phase 1 scores correlated with VMA (r = .52, p<.01). No other correlations
were significant. Correlations carried out on the autism data were significant for
phase 1 and discrimination ability (experiment 1) (r = .62, p<.05). There was also a
significant negative correlation between phase 2 scores and VMA (r = -.55, p<.05).
These latter findings suggest that a bias to encode perceptual information in autism is
Discussion
In the pre-test phase of the experiments, participants were presented with a range of
eleven colours for identification. Whilst some individuals with autism and MLD made
some errors there was no significant difference between groups and the majority of
expected to know all 11 basic colour terms by five years and the VMA means for all
groups were higher than this. The findings from experiment 1 were surprising given
Caron, Mottron, Berthiaume & Dawson; 2006). However, whilst participants with
autism performed at levels that were significantly better than chance, discrimination
In experiment 2, animals and colour patches were presented for paired learning. In
phase 1 of the experiment, the colours with which the animals were associated were
both widely separated in perceptual space and were also from different name
should yield correct performance. In phase 2 of the experiment however, all three
choice alternatives received the same name, so a memory strategy based on naming
qualities and ignoring the name classification of the presented stimuli would above-
this condition (although controls did not) indicating that they remembered the exact
shades of the paired colours, rather than relying on the category name. Whilst all of
these participants knew the relevant colour names, these appeared to influence their
colour perception to a far lesser degree than that of children with similar levels of
The correlations carried out on the data from the experiments revealed interesting
conditions. Within the typically developing group, the most verbally able children
experiment 2. Whilst discrimination in experiment 1 did not correlate with VMA for
the MLD controls, the phase 1 scores and VMA correlation approached significance.
Whilst MLD scores were poorer than those of TD participants, they resembled them
experiment 2, are surprising given empirical findings showing that colour stimuli are
encoded both perceptually and verbally by adults (e.g. Robeson & Davidoff, 2000;
Pilling et al., 2003). However, in experiment 2, attention was directed to both colours
and animals, and this may have reduced perceptual encoding of colour information.
Further, familarisation trials and test trials for phase 1 may have served to reinforce
the use of a verbal labelling strategy, which resulted in chance performance on phase
two.
The correlations carried out on the autism data showed that like TD participants,
interesting in that much of the empirical work that has supported enhanced perception
theories has been carried out with intellectually able individuals with autism.
However, in experiment 1, the upper range for discrimination scores was still lower
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than for the MLD group (19 MLD; 17 LFA). As was the case for the participants
without autism, there was a positive and significant correlation between VMA and
scores for phase 1 of experiment 2. However for phase 2, where performance was not
at chance, performance scores and VMA correlations were significant and negative,
showing that children with autism and low VMA retained unusually high levels of
features. However, whilst these changes influenced category re-allocation (e.g. cat to
dog category) in infants, such effects were not seen in adults (Rakison, 2000). The
pictures of objects for which verbal labels are available (Baldwin & Markham, 1989;
Schafer et al., 1999), and the close link between the onset of spontaneous exhaustive
sorting of object into groups and the naming spurt at 18 months (Gopnik & Meltzoff,
1997). If, as this evidence suggests, an early interplay between perceptual and
for the development of concepts and categories, then this raises important questions
about qualitatively atypical information processing in children for whom language has
been markedly delayed. Whilst most of the autistic participants knew colour names,
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without autism. For children with autism, the increased salience of perceptual
development. Late language competence may force autistic individuals to adopt novel
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Appendix 1
Stimuli used in Experiment 1
Discrimination Task
Practice Trials
Test Trials
2.5B6/6, 5B6/6, 7.5B6/6, 10B6/6
2.5Y6/6, 5Y6/6, 7.5Y6/6, 10Y6/6
2.5R6/6, 5R6/6, 7.5R6/6, 10R6/6
2.5G6/6, 5G6/6, 7.5G6/6, 10G6/6
Memory Task
Part One
Part Two
5R6/6, 1R6/6, 9R6/6
5B6/6, 1B6/6, 9B6/6
5G6/6, 1G6/6, 9G6/6
5Y6/6, 1Y6/6, 9G6/6
23
Table 1: Psychometric data for participants with autism and their controls.
TD Controls 11.00 .0
Table 4: Mean memory accuracy and standard deviations for the participants
with Autism and their controls on phase 1 and phase 2 of experiment 2.
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