(1) The purported evidence for neural filling-in is not evidence for filling-in, but just for long-range dynamic interactions. (2) Vision is perhaps not an “illusion,” but at any rate it is not “pictorial.” (3) The idea of the “world as an outside memory” as well as MacKay's “conditional readiness for action” may help approach an “enactive” theory of vision.

The dynamical hypothesis is strong in that, for it to be true, every cognitive phenomenon must be best modeled by a dynamical system. Depending on how it is interpreted, however, the hypothesis may be seen as probably false or even unfalsifiable. Strengthening the hypothesis to require unification, or at least coherence, across models in different cognitive domains alleviates this problem.

There is evidence that in women high levels of testosterone are associated with more sexual partners and more permissive sexual attitudes. If a similar relationship holds true for men, the higher basal testosterone levels of divorced and unmarried men may be caused by this relationship rather than by testosterone's effect on dominance striving.

Proximal mirroring of distal similarities is, at present, the only solution to the problem of representation that is both theoretically sound (for reasons discussed in the target article) and practically feasible (as attested by the performance of the Chorus model). Augmenting the latter by a capability to refer selectively to retinotopically defined object fragments should lead to a comprehensive theory of shape processing.

The species-specific organizational property of speech is a continual mouth open-close alternation, the two phases of which are subject to continual articulatory modulation. The cycle constitutes the syllable, and the open and closed phases are segments – vowels and consonants, respectively. The fact that segmental serial ordering errors in normal adults obey syllable structure constraints suggests that syllabic “frames” and segmental “content” elements are separately controlled in the speech production process. The frames may derive from cycles of mandibular oscillation present in humans from babbling onset, which are responsible for the open-close alternation. These communication- related frames perhaps first evolved when the ingestion-related cyclicities of mandibular oscillation (associated with mastication [chewing] sucking and licking) took on communicative significance as lipsmacks, tonguesmacks, and teeth chatters – displays that are prominent in many nonhuman primates. The new role of Broca's area and its surround in human vocal communication may have derived from its evolutionary history as the main cortical center for the control of ingestive processes. The frame and content components of speech may have subsequently evolved separate realizations within two general purpose primate motor control systems: (1) a motivation-related medial “intrinsic” system, including anterior cingulate cortex and the supplementary motor area, for self-generated behavior, formerly responsible for ancestral vocalization control and now also responsible for frames, and (2) a lateral “extrinsic” system, including Broca's area and surround, and Wernicke's area, specialized for response to external input (and therefore the emergent vocal learning capacity) and more responsible for content.

The following three points are made. One must consider not only the levels of circulating hormone but the target tissue upon which the hormone acts. Increased testosterone levels alone do not account for differences in displayed intermale aggression, because testosterone and social environment interact in complex ways to influence behavior. A given behavior can be triggered by multiple motivational systems.

Unfortunately, reading Chow's work is likely to leave the reader more confused than enlightened. My preferred solutions to the “controversy” about null- hypothesis testing are: (1) recognize that we really want to test the hypothesis that an effect is “small,” not null, and (2) use Bayesian methods, which are much more in keeping with the way humans naturally think than are classical statistical methods.

The case against analytical isomorphism is made within an evolutionary framework. The relevance to neural filling-in is discussed. Homomorphism is argued for as a conceptually superior substitute for isomorphism, and the implications for the personal/subpersonal distinction are explored.

The distinction at the heart of van Gelder's target article is one between digital computers and dynamical systems, but this distinction conflates two more fundamental distinctions in cognitive science that should be kept apart. When this conflation is undone, it becomes apparent that the computational hypothesis is not as dominant in contemporary cognitive science as van Gelder contends; nor has the dynamical hypothesis been neglected.

Research in expert categorization is consistent with the Schyns et al. claim that functional features are determined by constraints imposed by the learning history of the categorizer and the demands of the categorization task. However, the expertise work also suggests that a distinction should be drawn between the categorizer's perceptions of the constituent parts of the object and its functional features. Although experts and novices may parse a domain-specific object into the same parts, their featural interpretations of those parts may differ significantly.

Schyns, Goldstone & Thibaut present reasonable arguments for feature creation in category learning. We argue, however, that they do not provide unequivocal evidence either for the necessity or for the occurrence of feature creation. In an effort to sharpen the debate, we take the stand that a fixed feature approach is to be preferred in the absence of compelling evidence.

Pessoa et al. fail to make a clear distinction between visual perception and subjective visual awareness. Their most controversial claims, however, concern subjective visual awareness rather than visual perception: visual awareness is externalized to the “personal level,” thus denying the view that consciousness is a natural biological phenomenon somehow constructed inside the brain.

Chow's (1996) defense of the null-hypothesis significance-test procedure (NHSTP) is thoughtful and compelling in many respects. Nevertheless, techniques such as meta-analysis, power analysis, effect size estimation, and confidence intervals can be useful supplements to NHSTP in furthering the cumulative nature of behavioral research, as illustrated by the history of research on the spontaneous recovery of verbal learning.

The basal and reciprocal models of the relationship between androgen secretion and dominance are not mutually exclusive. Individuals may differ in basal levels of androgen secretion, reactivity to experiences, and androgen sensitivity. Early experiences might affect any of these parameters.

After a historical sketch of the dynamical hypothesis, we stress that it is a functionalist hypothesis. We then tackle the point of a dynamical approach to constituent structures and emphasize that dynamical modeling must be coupled with morphological analysis.

We applaud the spirit of MacNeilage's attempts to better explain the evolution and cortical control of speech by drawing on the vast literature in nonhuman primate neurobiology. However, he oversimplifies motor cortical fields and their known individual functions to such an extent that he undermines the value of his effort. In particular, MacNeilage has lumped together the functional characteristics across multiple mesial and lateral motor cortex fields, inadvertantly creating two hypothetical centers that simply may not exist.

Van Gelder seeks to distinguish between the computational and the dynamical hypotheses primarily on the basis of ontic criteria – the kind of systems cognitive agents really are. I suggest that this meets with mixed success. By shifting to epistemic criteria – what kind of explanations we require to understand cognitive agents – I suggest there is an easier and more intuitive way to distinguish between these two competing views of cognitive agents.

We agree with MacNeilage's claim that speech stems from a volitional vocalization pathway between the cingulate and the supplementary motor area (SMA). We add the vocal self- monitoring system as the first recruitment of the Broca-Wernicke circuit. SMA control for “frames” is supported by wrong consonant-vowel recurring utterance aphasia and an imaging study of quasi-reiterant speech. The role of Broca's area is questioned in the emergence of “content,” because a primary motor mapping, embodying peripheral constraints, seems sufficient. Finally, we reject a uniquely peripheral account of speech emergence.

Discriminating behavior depends on neural representations in which the sensory activity patterns guiding different responses are decorrelated from one another. Visual information can often be parsimoniously transformed into these behavioral bridge-locus representations within neuro-computational visuo-spatial maps. Isomorphic inverse-optical world representation is not the goal. Nevertheless, such useful transformations can involve neural filling-in. Such a subpersonal representation of information is consistent with personal-level vision theory.

This commentary questions the validity of the claim that new features can be constructed out of nothing during categorization. A minimal set of fixed features based on what human beings are able to detect is sufficient for categorization.