Commentary on Smith, J. D.; Shields, W. E. & Washburn, D. A.

Abstract: 111 words
Main Text: 558 words
References:  210 words
Total Text: 945 words

If metacognition exists in other species, how does it develop?

Ruth Campos

Psychology Department
Universidad Autónoma de Madrid
Departamento de Psicología Básica. Facultad de Psicología. Universidad Autónoma de Madrid
Madrid, 28049

34 913978572
Spain
ruth.campos@uam.es
 
 

Annette Karmiloff Smith

Neurocognitive Development Unit
Institute of Child Health
Neurocognitive Development Unit. Institute of Child Health. 30 Guildford Street.
London, WC1N 1EH
United Kingdom
44 0207 905 2754

a.karmilof-smith@ich.ucl.ac.uk
http://www.ich.ucl.ac.uk/units/ncdu/NDU_homepage.htm 
 

Abstract

In this commentary, we raise two issues.  First, we argue that in any species, the comparative study of metacognitive abilities must be  approached from a developmental perspective and not solely from the adult end state. This makes it possible to explore the trajectories by which different species reach their phenotypic outcome and whether different cognitive systems interact over developmental time.   Second, using our research comparing different genetic disorders in humans, we challenge the authors’ claim that it is unparsimonious to interpret the same performance in humans and animals in qualitatively different ways, because even the same overt behaviour in different groups of humans can be sustained by different underlying cognitive processes.

 

Text1 

Smith, Shields and Washburn are to be particularly commended for their synthesis of the research on animal metacognitive abilities and their stimulating attempt to establish a psychological interpretation of animal metacognitive performance via tasks tapping uncertainty monitoring. 

 

We are particularly concerned with the implications that the authors’ proposal has for the study of the progressive development of metacognitive abilities in humans as compared to other species.  We note that the authors seem to accept uncritically the fact that all the participants in the various studies they reviewed are adults.  In fact, this tends to be the general case in comparative psychology, even when another adult species is directly compared with human infants or children, be it in the domain of metacognition or other cognitive abilities.  Such an approach is, in our view, regrettable because, to understand the phenotypic outcome of any species (including human), it is vital to trace the developmental trajectory by which the ability is achieved (Karmiloff-Smith, 1998; Paterson et al., 1999; Piaget, 1952).  Only then can one judge if similar overt behaviour is underpinned by similar underlying cognitive processes. Taking a developmental perspective also makes it possible to ascertain whether metacognitive capacities interact over developmental time with other cognitive processes and whether this interaction is analogous in humans and other species. In other words, we believe that cross-species comparisons must involve a developmental perspective both theoretically and empirically.  This has proven crucial in the study of metacognitive abilities in humans (Karmiloff-Smith, 1992; Perner, 1991). Metacognition is not an all or none process.  It develops very progressively in human children. The question that remains is whether this progressive development is the case for those species that the authors claim to display aspects of metacognition.

 

Our second point concerns the issue of parsimony.  Normally, of course, one would want to consider similar behaviour between different groups (two groups of humans or comparing humans with other species) as indicating similar cognitive processes.  However, our work on normal development has demonstrated that at different ages children may display the same overt behaviour which is none the less underpinned by very different internal representations (Karmiloff-Smith, 1992).  And studies of atypical development suggest that, even when a clinical group attains the same behavioural scores as normal controls, the behaviours are often sustained by very different cognitive and brain processes in the two groups (Grice et al., 2001; Karmiloff-Smith, 1998).  For example, individuals with Williams syndrome (WS), a rare genetic disorder (Donnai & Karmiloff-Smith, 2000), display scores in the normal range on some face processing tasks.  However, in-depth studies revealed that while normal controls used configural processing, the participants with WS employed componential processing when looking at faces (Deruelle et al., 1999; Karmiloff-Smith, 1998).  A second example comes from reading.  Normal and WS participants, individually matched on reading scores, turned out to display very different strategies when learning to read new words, suggesting that each group had reached their reading scores via different developmental trajectories (Laing et al., 2001).  Such data reveal the need for caution when evaluating similar overt behaviour both within and across species. Would we want to equate parrot speech to human language?

 

In our view, the answers to both the issues we have raised in this commentary should be sought in the detailed study of the developmental trajectories that lead to the metacognitive abilities that any species displays.
 

 

References

Deruelle, C., Mancini, J., Livet, M. O., Casse-Perrot, C. & de Schonen, S. (1999). Configural and local processing of faces in children with Williams syndrome. Brain and Cognition, 41, 276-298.

Donnai, D. & Karmiloff-Smith, A. (2000). Williams syndrome: From genotype through to the cognitive phenotype. American Journal of Medical Genetics: Seminars in Medical Genetics. 97 (2), 164-171.

Grice, S., Spratling, M.W., Karmiloff-Smith, A., Halit, H., Csibra, G., de Haan, M., & Johnson, M.H. (2001). Disordered visual processing and oscillatory brain activity in autism and Williams Syndrome. Neuroreport, 12, 2697-2700.

Karmiloff-Smith, A. (1992). Beyond Modularity: A Developmental Perspective on Cognitive Science.  Cambridge, Mass.: MIT Press/Bradford Books.

Karmiloff-Smith, A. (1998). Development itself is the key to understanding developmental disorders. Trends in Cognitive  Sciences, 2, 10, 389-398.

Laing, E., Hulme, C., Grant, J. & Karmiloff-Smith, A. (2001). Learning to Read in Williams Syndrome: Looking Beneath the Surface of Atypical Reading Development. Journal of Child Psychology and Psychiatry, 42, 6, 729-739.

Paterson, S.J., Brown, J. H. , Gsödl, M. K. , Johnson, M. H. & Karmiloff-Smith, A. Cognitive Modularity and Genetic Disorders. Science, 286, 5448 Dec 17, 1999: 2355-2358.

Perner, J. (1991). Understanding the Representational Mind. Cambridge, Mass.: MIT Press.

Piaget, J. (1952). The Origins of Intelligence in Children. New York: International University Press.