The mechanics of walking restructured the pelvis and narrowed the birth-canal that selected for delays in skeletal ossification. Prolonged phases of fetal maturation increased the mass and volume of the brain relative to adult body-size, as encephalization increased. Thus, bipedal- walking and episodic increases in hominine body size probably triggered selection for neonatal skeletal immaturity that led to encephalization.

Although Bloom gives more credit to social cognition (mind reading) than do most other theorists of word learning, he does not go far enough. He still relies fundamentally on a learning process of association (or mapping), neglecting the joint attentional and cultural learning skills from which linguistic communication emerges at one year of age.

Using explicit memory measures, Cowan predicts a new circumstance in which the central capacity limit of 4 chunks should obtain. Supporting results for such an experiment, using continuous old-new recognition, are described. With implicit memory measures, Cowan assumes that short-term repetition priming reflects the central capacity limit. I argue that this phenomenon instead reflects limits within individual perceptual processing modules.

First, we discuss issues raised with respect to the Theory of Event Coding (TEC)'s scope, that is, its limitations and possible extensions. Then, we address the issue of specificity, that is, the widespread concern that TEC is too unspecified and, therefore, too vague in a number of important respects. Finally, we elaborate on our views about TEC's relations to other important frameworks and approaches in the field like stages models, ecological approaches, and the two-visual-pathways model.

Bloom's book underscores the importance of specifying the role of words and grammar in cognition. We propose that the cognitive power of language lies in the lexicon rather than grammar. We suggest ways in which studies involving children and patients with aphasia can provide insights into the basis of abstract cognition in the domain of number and mathematics.

I compare the concepts of “activation” and “storage” as foundations of short-term memory, and suggest that an attention-based view of STM does not need to posit specialized short-term stores. In particular, no compelling evidence supports the hypothesis of time-limited stores. Identifying sources of activation, examining the role of activated procedural knowledge, and studying working memory development are central issues in modelling capacity-limited focal attention.

Researchers studying primate brain allometry often focus on departures from allometry more than the allometric relationships themselves because only the former reveal what brain regions and behavioral-cognitive abilities were the focus of selection. Allometric departures for the human brain provide insights into hominid brain evolution and cast doubt on the suggestion that the large human cerebral cortex is a “spandrel.”

Many current neurophysiological, psychophysical, and psychological approaches to vision rest on the idea that when we see, the brain produces an internal representation of the world. The activation of this internal representation is assumed to give rise to the experience of seeing. The problem with this kind of approach is that it leaves unexplained how the existence of such a detailed internal representation might produce visual consciousness. An alternative proposal is made here. We propose that seeing is a way of acting. It is a particular way of exploring the environment. Activity in internal representations does not generate the experience of seeing. The outside world serves as its own, external, representation. The experience of seeing occurs when the organism masters what we call the governing laws of sensorimotor contingency. The advantage of this approach is that it provides a natural and principled way of accounting for visual consciousness, and for the differences in the perceived quality of sensory experience in the different sensory modalities. Several lines of empirical evidence are brought forward in support of the theory, in particular: evidence from experiments in sensorimotor adaptation, visual “filling in,” visual stability despite eye movements, change blindness, sensory substitution, and color perception.

The stratification in depth of chromatically homogeneous overlapping figures depends on a minimization rule which assigns the status of being “in front” to the figure that requires the formation of shorter modal contours. This rule has been proven valid also in birds, whose visual neuroanatomy is radically different from that of other mammals, thus suggesting an example of evolutionary convergence toward a perceptual universal. [Shepard]

Humphreys & Forde concentrate on the living/nonliving dissociation. However, further dissociations have been reported, including selective loss or preservation in recognizing body parts and numbers. This commentary outlines the relevance of the number category for understanding the organising principles of semantic memory.

Humphreys and Forde argue that semantic memory is divided into separate substores for different kinds of information. However, the neuro-imaging results cited in support of this view are inconsistent and often methodologically and statistically unreliable. Our own data indicate no regional specialisation as a function of semantic category or domain and support instead a distributed unitary account.

Shepard's notion of “internalisation” is better interpreted as a simile than a metaphor. A fractal encoding model of visual perception is sketched, in which image elements are transformed in such a way as to maximise symmetry with the current input. This view, in which the transforming system embodies what has been internalised, resolves some problems raised by the metaphoric interpretation. [Hecht; Shepard]

Partial matching theory, which maintains that some memory representations of target items in immediate memory are overwritten by others, can predict both a “theoretical” and an “actual” maximum memory span provided no chunking takes place during presentation. The latter is around 4 ± 2 items, the exact number being determined by the degree of similarity between the memory representations of two immediately successive target items.

Bloom provides a masterful synthesis of recent advances in word-learning, placing them within the framework of abiding theoretical issues. I will augment and challenge his approach by underscoring the significance of word extension for questions concerning (a) the origin and evolution of infants' expectations, and (b) domain-specificity in word-learning.

Let us simplify the problem of “consciousness” or “visual consciousness”: Seeing is feeling. The difference between an optical transducer/effector that merely interacts with optical input, and a conscious system that sees, is that there is something it feels like for that conscious system to see, and that system feels that feeling. All talk about “internal representations” and internal or external difference registration or detection, and so on, is beside the point. The point is that what is seen is felt, not merely registered, processed, and acted upon. To explain consciousness in terms of sensorimotor action, one has to explain why and how any of that processing is felt; otherwise one is merely giving an optokinetic explanation of I/O (Input/Ouput) capacities (and of whether those capacities are actually or optimally generated by sensorimotor contingency processors, analog representations, symbolic representations, or other forms of internal structure/process), not of the fact that they are felt. Nor will it do to say “qualia are illusions.” Qualia are feelings. Am I under the illusion that I am seeing (i.e., feeling) something right now? What is the truth then? That I am not feeling, but merely acting? No, I'm afraid Descartes had it right. Certain things are not open to doubt. They either need to be explained, or passed over in silence, in favor of the unfelt correlated functions that we can explain (Harnad 1995; 2000; 2001).

The existence of linked regularities in size among brain components across species is, by itself, not a strong argument against the importance of behavioral selection in brain evolution. A careful consideration of hominid brain evolution suggests that brain components can change their scaling relationships over time, and that behavioral selection was likely crucial. The best neuroanatomical index of a given behavioral ability can only be determined empirically, not through comparative analysis of brain anatomy alone.

Visual conscious perception could be grounded in a nonconscious sensorimotor domain. Although invisible, information can be processed up to the level of response activation. Moreover, these nonconscious processes are modified by actual intentions. This notion bridges a gap in the theoretical framework of O'Regan & Noë.

This book is an excellent and accessible overview of the position that children learn the meanings of words by applying a variety of nonlinguistic cognitive tools to the problem. We take issue with Bloom's emphasis on Theory of Mind as an explanatory mechanism for language learning; and with his claim that only unitary objects are nameable.

Constraint has played a major role in brain evolution, but cannot tell the whole story. In primates, adaptive specialization is suggested by the existence of a covarying visual system, and may explain some residual variation in the constraint model. Adaptation may also appear at the microstructural level and in the globally integrated system of brain, body, life history and behavior.

Memory and forgetting are inextricably intertwined. Any account of short-term memory (STM) should address the following question: If three, four, or five chunks are being held in STM, what happens after attention is diverted?