Nel campo delle scienze cognitive molti oggi condividono l’ipotesi che siano necessari differenti tipi di rappresentazioni per modellare i sistemi cognitivi sia naturali, sia artificiali. Si considerino le rappresentazioni basate su reti neurali, i formalismi simbolici e rappresentazioni analogiche quali rappresentazioni diagrammatiche o modelli mentali. Tutti questi metodi hanno successo nello spiegare e modellare alcune classi di fenomeni cognitivi, ma nessuno è in grado di rendere conto di tutti gli aspetti della cognizione. A partire da queste considerazioni, riteniamo che sistemi (...) intelligenti e architetture cognitive possano trarre vantaggio dalla combinazione di sistemi di rappresentazione diversi. Si pone allora il problema di fare interagire rappresentazioni di natura differente in maniera cognitivamente e teoricamente fondata. La nostra ipotesi è che gli spazi concettuali possano offrire una sorta di lingua comune, che consentirebbe di integrare e generalizzare molti aspetti delle impostazioni sopra menzionate, superando i limiti delle varie proposte intese singolarmente. (shrink)

Amit's Hebbian model risks being overexplanatory, since it does not depend on specific physiological modelling of cortical ANNs, but concentrates on those phenomena which are modelled by a large class of ANNs. While offering a strong demonstration of the presence of Hebb's “cell assemblies,” it does not offer an equal account of Hebb's “phase sequence” concept.

According to one productive and influential approach to cognition, categorization, object recognition, and higher level cognitive processes operate on a set of fixed features, which are the output of lower level perceptual processes. In many situations, however, it is the higher level cognitive process being executed that influences the lower level features that are created. Rather than viewing the repertoire of features as being fixed by low-level processes, we present a theory in which people create features to subserve the representation (...) and categorization of objects. Two types of category learning should be distinguished. Fixed space category learning occurs when new categorizations are representable with the available feature set. Flexible space category learning occurs when new categorizations cannot be represented with the features available. Whether fixed or flexible, learning depends on the featural contrasts and similarities between the new category to be represented and the individual's existing concepts. Fixed feature approaches face one of two problems with tasks that call for new features: If the fixed features are fairly high level and directly useful for categorization, then they will not be flexible enough to represent all objects that might be relevant for a new task. If the fixed features are small, subsymbolic fragments (such as pixels), then regularities at the level of the functional features required to accomplish categorizations will not be captured by these primitives. We present evidence of flexible perceptual changes arising from category learning and theoretical arguments for the importance of this flexibility. We describe conditions that promote feature creation and argue against interpreting them in terms of fixed features. Finally, we discuss the implications of functional features for object categorization, conceptual development, chunking, constructive induction, and formal models of dimensionality reduction. Key Words: concept learning; conceptual development; features; perceptual learning; stimulus encoding. (shrink)

Cortical reverberations may induce synaptic changes that underlie developmental plasticity as well as long-term memory. They may be especially important for the consolidation of synaptic changes. Reverberations in cortical networks should have particular significance during development, when large numbers of new representations are formed. This includes the formation of representations across different sensory modalities.

A distinction should be made between the formation of stimulus-driven associations and cognitive concepts. To test the learning mode of a neural network, we propose a simple and classic input-output test: the discrimination shift task. Feed-forward PDP models appear to form stimulus-driven associations. A Hopfield network should be extended to apply the test.

Amit defines cell assemblies aslocal cortical neuron populationswith strong internal connections. However, Hebb himself proposed that cell assemblies are distributed over different cortical areas (nonlocal ortranscortical assemblies). We review evidence from cognitive neuroscience and neuropsychology supporting the assumption that cell assemblies are transcortical.

Amit's “Attractor Neural Network” perspective on cognition raises difficult technical problems already met by prior dynamical models. This commentary sketches briefly some of them concerning the internal topological structure of attractors, the constituency problem, the possibility of activating simultaneously several attractors, and the different kinds of dynamical structures one can use to model brain activity: point attractors, strange attractors, synchronized arrays of oscillators, synfire chains, and so forth.

The Miyashita experiments are very interesting and the results should be examined from a viewpoint of attractor dynamics. Amit's target article shows a path toward realistic modeling by artificial neural networks (ANN), but it is not necessarily the only one. I introduce another model that can explain a substantial part of the empirical observations and makes an interesting prediction. This model consists of such units that have nonmonotonic input-output characteristics with local inhibition neurons.

Every immediate memory is unique; it is therefore unlikely to consist of an attractor or even a combination of attractors. In the present state of knowledge about the chemistry of synaptic transmission, there is no reason to look beyond neurons that directly receive sensory afferents for the afterdischarges that correspond to active memories.

Hebbian cell-assembly theory and attractor networks are good starting points for modeling cortical processing. Detailed cell models can be useful in understanding the dynamics of attractor networks. Cell assemblies are likely to be distributed, with the cortical column as the local processing unit. Synaptic memory may be dominant in all but the first couple of seconds.

Hebbian mechanisms are justified according to their functional utility in an evolutionary sense. The selective advantage of correlating content-contingent stimuli reflects the putative common cause of temporally or spatially contiguous inputs. The selective consequences of such correlations are discussed by using examples from the evolution of signal form in sexual selection and model-mimic coevolution. We suggest that evolutionary justification might be considered in addition to neurophysiology plansibility when constructing representational models.

Amit argues that the local neuronal spike rate that persists (reverberating) in the absence of the eliciting stimulus represents the code of the eliciting stimulus. Based on the general argument that the inferred functional meaning of reverberation depends in part on the type of representational assumptions, reverberations may only be important for the encoding of contextual information.

Amit's efforts to provide stronger theoretical and empirical support for Hebb's cell-assembly concept is admirable, but we have serious reservations about the perspective presented in the target article. For Hebb, the cell assembly was a building block; by contrast, the framework proposed here eschews the need to fit the assembly into a broader picture of its function.

Further tests of Amit's model are indicated. One strategy is to use the apparent coding sparseness of the model to make predictions about coding sparseness in Miyashita's network. A second approach is to use memory overload to induce false positive responses in modules and biological systems. In closing, the importance of temporal coding and timing requirements in developing biologically plausible attractor networks is mentioned.

The concept of an attractor in a mathematical dynamical system is reviewed. Emphasis is placed on the distinction between a cell assembly, the corresponding attractor, and the attractor dynamics. The biological significance of these entities is discussed, especially the question of whether the representation of the stimulus requires the full attractor dynamics, or merely the cell assembly as a set of reverberating neurons. Comparison is made to Freeman's study of dynamic patterns in olfaction.

In recent years, many philosophers have supposed that perceptual representations have propositional content. A prominent rationale for this supposition is the assumption that perceptions may justify beliefs, but this rationale can be doubted. This rationale may be doubted on the grounds that there do not seem to be any viable characterizations of the belief-justifying propositional contents of perceptions. An alternative is to model perceptual representations as marks in a perceptual similarity space. A mapping can be defined between points in perceptual (...) similarity space and points in an objective quality space. The correctness of perceptual representation can then be defined as a kind of accuracy of mapping rather than as the truth of a proposition. The phenomenon of seeing-as can be accounted for as a matter of the location of marks in perceptual similarity space relative to other marks in perceptual similarity space. Perceptual representations, on this account, will not justify beliefs, but they may nonetheless guide judgment. (shrink)

This commentary questions the target articles inferences from a limited set of empirical data to support this model and conceptual scheme. Especially questionable is the attribution of internal representation properties to an assembly of cells in a discrete cortical module firing at a discrete attractor frequency. Alternative inferences are drawn from cortical cooling and cell-firing data that point to the internal representation as a broad and specific cortical network defined by cortico-cortical connectivity. Active memory, it is proposed, consists in the (...) sustained activation of the component neuron populations of the network. (shrink)

Recurrent excitation is experimentally well documented in cortical populations. It provides for intracortical excitatory biases that linearize negative feedback interactions and induce macroscopic state transitions during perception. The concept of the local neighborhood should be expanded to spatial patterns as the basis for perception, in which large areas of cortex are bound into cooperative behavior with near-silent columns as important as active columns revealed by unit recording.

A theory of representation is incomplete if it states “representations areX” whereXcan be symbols, cell assemblies, functional states, or the flock of birds fromTheaetetus, without explaining the nature of the link between the universe ofXs and the world. Amit's thesis, equating representations with reverberations in Hebbian cell assemblies, will only be considered a solution to the problem of representation when it is complemented by a theory of how a reverberation in the brain can be a representation of anything.

The cell assembly is an important concept for cognitive psychology. Cognitive processing will to a large extent depend on the relations that can exist between different assemblies. A potential relation between assemblies can already be seen in the occurrence of (classical) conditioning. However, the resulting associations between assemblies only produce behavioristic processing or so-called regular computation. Higher-level cognitive abilities most likely result from nonregular computation. I discuss the possibility of this form of computation in terms of cell assemblies.

The cell assembly as a simple attractor cannot explain many cognitive phenomena. It must be a highly structured network that can sustain highly structured excitation patterns. Moreover, a cell assembly must be more widely distributed in space than on a square millimeter.

Amit's work addresses a critical issue in cognitive science: the structure of neural representations. The use of Hebbian cell assemblies is a positive step, and we now need to consider its role in a larger cognitive theory. When considering the dynamics of a system built out of attractors, a more limited version of reverberation becomes necessary.

Interpreting the Miyashita et al. experiments in terms of a cellassembly representation does not adequately explain the performance of Miyashita's monkeys on novel stimuli. We will argue that the latter observations point to acompositionalrepresentation and suggest a dynamics involving rapid and reversible binding of distinct activity patterns.

The neurophysiological evidence from the Miyashita group's experiments on monkeys as well as cognitive experience common to us all suggests that local neuronal spike rate distributions might persist in the absence of their eliciting stimulus. In Hebb's cell-assembly theory, learning dynamics stabilize such self-maintaining reverberations. Quasi-quantitive modeling of the experimental data on internal representations in association-cortex modules identifies the reverberations (delay spike activity) as the internal code (representation). This leads to cognitive and neurophysiological predictions, many following directly from the language (...) used to describe the activity in the experimental delay period, others from the details of how the model captures the properties of the internal representations. (shrink)

The context of the target article is delimited again, underlining the intended locationof the argument in the bottomup hierarchy of brain study. The central message is that collective delay activity distributions (reverberations) in cortical modules extend the role of a spike (a potentialinformation carrier across long distances) to an active memory of structured, learned information that can be carried across long time intervals. Moreover, the population code of the reverberations makes them readable down the cortical processing stream. Most of the (...) critical comments are then interpreted and addressed in relation to misreading of the proper context. The price for the limitation of the context (in cognitive, behavioral, and computational terms) is compared with the advantages of a clear, direct contact with experiment on the one hand and with a well controlled body of modeling and analysis on the other. (shrink)

Persistent activity can be the product of mechanisms other than attractor reverberations. The single-unit data presented by Amit cannot discriminate between the different mechanisms. In fact, single-unit data do not appear to be adequate for testing neural network models.

Mental imagery (varieties of which are sometimes colloquially refered to as “visualizing,” “seeing in the mind's eye,” “hearing in the head,” “imagining the feel of,” etc.) is quasi-perceptual experience; it resembles perceptual experience, but occurs in the absence of the appropriate external stimuli. It is also generally understood to bear intentionality (i.e., mental images are always images of something or other), and thereby to function as a form of mental representation. Traditionally, visual mental imagery, the most discussed variety, was thought (...) to be caused by the presence of picturelike representations (mental images) in the mind, soul, or brain, but this is no longer universally accepted. (shrink)

differentiaily rated pairwise similarity when confronted with two pairs of objects, each revolving in a separate window on a computer screen. Subject data were pooled using individually weighted MDS (ref. 11; in all the experiments, the solutions were consistent among subjects). In each trial, the subject had to select among two pairs of shapes the one consisting of the most similar shapes. The subjects were allowed to respond at will; most responded within 10 sec. Proximity (that is, perceived similarity) tables (...) derived from the judgments were processed to verify their degree of transitivity (4% of all triplets were found intransitive) and then submitted to MDS. In the long-term memory (LTM) variant of this experiment, the subjects were first trained to associate a label (a three-letter nonsensical string, such as "BON" or "POM") with each object and then carried out the pairs of pairs comparison task from memory, prompted by the object labels rather than by the objects themselves. Six subjects participated in each of the two LTM experiments (Star and Triangle). The subjects were taught each shape in a separate session and had to discriminate between that shape and six similar nontargets from various viewpoints. Training continued until the recognition rate reached 90%, over a period of several days. The subjects were never exposed to more than one target in one session and were not told the ultimate purpose of the experiment. After 2 to 3 days of rest, they were tested with questions such as: "is the BON more similar to POM than TOC to ROX?", for all pairs of pairs of stimuli. In the LTM experiments, 8% of the.. (shrink)

The statistical structure of a class of objects such as human faces can be exploited to recognize familiar faces from novel viewpoints and under variable illumination conditions. We present computational and psychophysical data concerning the extent to which class-based learning transfers or generalizes within the class of faces. We rst examine the computational prerequisite for generalization across views of novel faces, namely, the similarity of di erent faces to each other. We next describe two computational models which exploit the similarity (...) structure of the class of faces. The performance of these models constrains hypotheses about the nature of face representation in human vision, and supports the notion that human face processing operates in a class-based fashion. Finally, we relate the computational data to well-established ndings in the human memory literature concerning the relationship between the typicality and recognizability of faces. (shrink)

Computer vision systems are, on most counts, poor performers, when compared to their biological counterparts. The reason for this may be that computer vision is handicapped by an unreasonable assumption regarding what it means to see, which became prevalent as the notions of intrinsic images and of representation by reconstruction took over the field in the late 1970’s. Learning from biological vision may help us to overcome this handicap.

In this article we present an advanced version of Dual-PECCS, a cognitively-inspired knowledge representation and reasoning system aimed at extending the capabilities of artificial systems in conceptual categorization tasks. It combines different sorts of common-sense categorization (prototypical and exemplars-based categorization) with standard monotonic categorization procedures. These different types of inferential procedures are reconciled according to the tenets coming from the dual process theory of reasoning. On the other hand, from a representational perspective, the system relies on the hypothesis of conceptual (...) structures represented as heterogeneous proxytypes. Dual-PECCS has been experimentally assessed in a task of conceptual categorization where a target concept illustrated by a simple common-sense linguistic description had to be identified by resorting to a mix of categorization strategies, and its output has been compared to human responses. The obtained results suggest that our approach can be beneficial to improve the representational and reasoning conceptual capabilities of standard cognitive artificial systems, and –in addition– that it may be plausibly applied to different general computational models of cognition. The current version of the system, in fact, extends our previous work, in that Dual-PECCS is now integrated and tested into two cognitive architectures, ACT-R and CLARION, implementing different assumptions on the underlying invariant structures governing human cognition. Such integration allowed us to extend our previous evaluation. (shrink)

During the last decades, many cognitive architectures (CAs) have been realized adopting different assumptions about the organization and the representation of their knowledge level. Some of them (e.g. SOAR [35]) adopt a classical symbolic approach, some (e.g. LEABRA[ 48]) are based on a purely connectionist model, while others (e.g. CLARION [59]) adopt a hybrid approach combining connectionist and symbolic representational levels. Additionally, some attempts (e.g. biSOAR) trying to extend the representational capacities of CAs by integrating diagrammatical representations and reasoning are (...) also available [34]. In this paper we propose a reflection on the role that Conceptual Spaces, a framework developed by Peter G¨ardenfors [24] more than fifteen years ago, can play in the current development of the Knowledge Level in Cognitive Systems and Architectures. In particular, we claim that Conceptual Spaces offer a lingua franca that allows to unify and generalize many aspects of the symbolic, sub-symbolic and diagrammatic approaches (by overcoming some of their typical problems) and to integrate them on a common ground. In doing so we extend and detail some of the arguments explored by G¨ardenfors [23] for defending the need of a conceptual, intermediate, representation level between the symbolic and the sub-symbolic one. In particular we focus on the advantages offered by Conceptual Spaces (w.r.t. symbolic and sub-symbolic approaches) in dealing with the problem of compositionality of representations based on typicality traits. Additionally, we argue that Conceptual Spaces could offer a unifying framework for interpreting many kinds of diagrammatic and analogical representations. As a consequence, their adoption could also favor the integration of diagrammatical representation and reasoning in CAs. (shrink)