The isomorphism constraint places plausible limits on the use of third-person evidence to explain color experience but poses no difficulty for functionalists; they themselves argue for just such limits. Palmer's absent qualia claim is supported by neither the Color Machine nor Color Room examples. The nature of color experience depends on relations external to the color space, as well as internal to it.

Two standard epistemological accounts are conflated in Dienes & Perner's account of knowledge, and this conflation requires the rejection of their four conditions of knowledge. Because their four metarepresentations applied to the explicit-implicit distinction are paired with these conditions, it follows by modus tollens that if the latter are inadequate, then so are the former. Quite simply, their account misses the link between true reasoning and knowledge.

To deal with syntactic structure, one needs to go beyond a simple model based on associative structures, and to adopt a dynamical systems perspective, where each phrase and sentence of a language is represented as a trajectory in a syntactic phase space. Neural assemblies could possibly be used to produce dynamics that in principle could handle syntax along these lines.

During active vision, the eyes continually scan the visual environment using saccadic scanning movements. This target article presents an information processing model for the control of these movements, with some close parallels to established physiological processes in the oculomotor system. Two separate pathways are concerned with the spatial and the temporal programming of the movement. In the temporal pathway there is spatially distributed coding and the saccade target is selected from a “salience map.” Both pathways descend through a hierarchy of levels, the lower ones operating automatically. Visual onsets have automatic access to the eye control system via the lower levels. Various centres in each pathway are interconnected via reciprocal inhibition. The model accounts for a number of well-established phenomena in target-elicited saccades: the gap effect, express saccades, the remote distractor effect, and the global effect. High-level control of the pathways in tasks such as visual search and reading is discussed; it operates through spatial selection and search selection, which generally combine in an automated way. The model is examined in relation to data from patients with unilateral neglect.

In his target article, Pulvermüller addresses the issue of word localization in the brain. It is not clear, however, how cell assemblies are localized in the case of sensory deprivation. Pulvermüller's claim is that words learned via other modalities (i.e., sign languages) should be localized differently. It is argued, however, based on experimental and theoretical ground, that they should be found in a similar place.

Palmer's main intuition pump, the “color machine,” greatly underestimates the complexity of a system isomorphic in color experience to humans. The neuroscientific picture of this complexity makes it clear that the brain actively produces our experiences by processes that science can investigate, thereby supporting functionalism and leaving no (color) room for a passive observer to witness subisomorphic experiential differences.

Caplan & Waters's neuropsychological evidence for two types of verbal working memory rests entirely on a very restricted definition of “syntactic complexity,” one in terms of word order. This opens the possibility that the dissociation they observe relates to the differential use of word-order strategies rather than to the structure of verbal working memory.

New experimental evidence throws doubt on postulating no relationship between saccade control and visual object recognition. The control of saccades during reading depends on the perceptual system mediating object recognition.

Pylyshyn claims that if a system is cognitively penetrable, its function depends in a semantically coherent way to the organism's goals and beliefs. He rejects evidence of attentional modulation observed in neurons within the visual system, claiming that any modulation seen is not logically related to goals and behavior. I present some of this evidence and claim that it is connected in exactly the way Pylyshyn requires and thus it refutes his main thesis.

Dienes & Perner propose a theory of implicit and explicit knowledge that is not entirely complete. It does not address many of the empirical issues, nor does it explain the difference between implicit and explicit learning. It does, however, provide a possible unified explanation, as opposed to the more binary theories like the systems and the processing theories of implicit and explicit memory. Furthermore, it is consistent with a theory in which implicit learning is viewed as based on the mechanisms of the cognitive architecture, and explicit learning as strategies that exploit these mechanisms.

We have shown that FEF lesion-induced extinction could be compensated for by changing the relative temporal onsets of two targets presented on either side of the midline. Monkeys were trained to make saccades to either of two identical visual stimuli presented with various stimulus onset asynchronies (SOA). In intact animals the targets were chosen with equal probability when they appeared simultaneously. After unilateral FEF lesions an SOA of 67–116 msec had to be introduced, with the contralesional target appearing first, to obtain equal probability choice. With a smaller target separation, averaging saccades occurred with highest frequency at similar SOAs. Our findings suggest that neglect may be attributable to more time being required in the damaged hemisphere for converting sensory information into motor responses.

We apply Dienes & Perner's (D&P's) framework to the automatic/nonautomatic processing contrast. Our analysis leads to the conclusion that automatic and nonautomatic processing result in representations that have explicit results. We propose equating consciousness with explicitness of aspects rather than with full explicitness as defined by D&P.

The Hebbian view of word representation is challenged by findings of task (level of processing)-dependent, event-related potential patterns that do not support the notion of a fixed set of neurons representing a given word. With cross-language phonological reliability encoding more asymmetrical left hemisphere activity is evoked than with word comprehension. This suggests a dynamical view of the brain as a self-organizing, connectivity-adjusting system.

The originator of the notion of structural isomorphism was the philosopher Roy Wood Sellars. Many modern philosophers are unaware how this notion vitiates their attacks on the concept of an internal sensory presentation. His view that this allowed for corrective feedback undercuts Palmer's belief that there is a mapping of objects. The privacy of subjective experience is also shown not to be inviolable.

Expert perceivers may learn more than just where to apply visual processing, or which part of the output from the visual system to attend to. Their early visual system may be modified, as a result of their specific needs, through a process of early visual learning. We argue that this is, in effect, a form of long-term, indirect cognitive penetration of early vision.

In challenging current conceptions of the role of working memory in sentence processing, Caplan & Waters consider studies comparing young and older adults on sentence processing. This commentary raises two challenges to Caplan & Waters's conclusions: first, working memory tasks appear to be age invariant. Second, the production of complex syntactic constructions appears not to be age invariant.

Implicit knowledge is perhaps better understood as latent knowledge so that it is readily apparent that it contrasts with explicit knowledge in terms of the form of the knowledge representation, rather than by definition in terms of consciousness or awareness. We argue that as a practical matter any definition of the distinction between implicit and explicit knowledge further involves the notion of control.

Pulvermüller's discussion needs more explanation of how the proposed assemblies remain assembled after formation and how they can be accessed later among all the possible assemblies, many of which involve many of the same neurons. Alternative Hebbian strengthening mechanisms may provide additional information, and, developmental studies of the assemblies might provide insights into their evolution.

Findlay & Walker's target article questions whether covert attention plays any role in normal visual scanning (overt attention). My commentary suggests that there is indeed a very close link between the processes that govern covert and overt attention.

Even though there is ample evidence from the sentence- comprehension literature for specialized working memory systems in normal and patient populations, some open questions remain. One of them is an explanation for a missing “post-interpretive” processing deficit in a variety of accuracy-judgment tasks in an aphasic patient with a severe verbal working memory problem.