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Nancy Kanwisher

Publications and source records attributed to Nancy Kanwisher.

15 recordsLinked to original sources

Location and spatial profile of category-specific regions in human extrastriate cortex.

Subjects were scanned in a single functional MRI (fMRI) experiment that enabled us to localize cortical regions in each subject in the occipital and temporal lobes that responded significantly in a variety of contrasts: faces>objects, body parts>objects, scenes>objects, objects>scrambled objects, and moving>stationary stimuli. The resulting activation maps were co-registered across subjects using spherical surface coordinates [Fischl et al., Hum Brain Mapp 1999;8:272-284] to produce a "percentage overlap map" indicating the percentage of subjects who showed a significant response for each contrast at each point on the surface. Prominent among the overlapping activations in these contrasts were the fusiform face area (FFA), extrastriate body area (EBA), parahippocampal place area (PPA), lateral occipital complex (LOC), and MT+/V5; only a few other areas responded consistently across subjects in these contrasts. Another analysis showed that the spatial profile of the selective response drops off quite sharply outside the standard borders of the FFA and PPA (less so for the EBA and MT+/V5), indicating that these regions are not simply peaks of very broad selectivities spanning centimeters of cortex, but fairly discrete regions of cortex with distinctive functional profiles. The data also yielded a surprise that challenges our understanding of the function of area MT+: a higher response to body parts than to objects. The anatomical consistency of each of our functionally defined regions across subjects and the spatial sharpness of their activation profiles within subjects highlight the fact that these regions constitute replicable and distinctive landmarks in the functional organization of the human brain.

Adult↗

Separate face and body selectivity on the fusiform gyrus.

Recent reports of a high response to bodies in the fusiform face area (FFA) challenge the idea that the FFA is exclusively selective for face stimuli. We examined this claim by conducting a functional magnetic resonance imaging experiment at both standard (3.125 x 3.125 x 4.0 mm) and high resolution (1.4 x 1.4 x 2.0 mm). In both experiments, regions of interest (ROIs) were defined using data from blocked localizer runs. Within each ROI, we measured the mean peak response to a variety of stimulus types in independent data from a subsequent event-related experiment. Our localizer scans identified a fusiform body area (FBA), a body-selective region reported recently by Peelen and Downing (2005) that is anatomically distinct from the extrastriate body area. The FBA overlapped with and was adjacent to the FFA in all but two participants. Selectivity of the FFA to faces and FBA to bodies was stronger for the high-resolution scans, as expected from the reduction in partial volume effects. When new ROIs were constructed for the high-resolution experiment by omitting the voxels showing overlapping selectivity for both bodies and faces in the localizer scans, the resulting FFA* ROI showed no response above control objects for body stimuli, and the FBA* ROI showed no response above control objects for face stimuli. These results demonstrate strong selectivities in distinct but adjacent regions in the fusiform gyrus for only faces in one region (the FFA*) and only bodies in the other (the FBA*).

Brain Mapping↗

Non-symbolic arithmetic in adults and young children.

Five experiments investigated whether adults and preschool children can perform simple arithmetic calculations on non-symbolic numerosities. Previous research has demonstrated that human adults, human infants, and non-human animals can process numerical quantities through approximate representations of their magnitudes. Here we consider whether these non-symbolic numerical representations might serve as a building block of uniquely human, learned mathematics. Both adults and children with no training in arithmetic successfully performed approximate arithmetic on large sets of elements. Success at these tasks did not depend on non-numerical continuous quantities, modality-specific quantity information, the adoption of alternative non-arithmetic strategies, or learned symbolic arithmetic knowledge. Abstract numerical quantity representations therefore are computationally functional and may provide a foundation for formal mathematics.

Adult↗

Visual recognition: as soon as you know it is there, you know what it is.

What is the sequence of processing steps involved in visual object recognition? We varied the exposure duration of natural images and measured subjects' performance on three different tasks, each designed to tap a different candidate component process of object recognition. For each exposure duration, accuracy was lower and reaction time longer on a within-category identification task (e.g., distinguishing pigeons from other birds) than on a perceptual categorization task (e.g., birds vs. cars). However, strikingly, at each exposure duration, subjects performed just as quickly and accurately on the categorization task as they did on a task requiring only object detection: By the time subjects knew an image contained an object at all, they already knew its category. These findings place powerful constraints on theories of object recognition.

Adult↗

Face perception: domain specific, not process specific.

Evidence that face perception is mediated by special cognitive and neural mechanisms comes from fMRI studies of the fusiform face area (FFA) and behavioral studies of the face inversion effect. Here, we used these two methods to ask whether face perception mechanisms are stimulus specific, process specific, or both. Subjects discriminated pairs of upright or inverted faces or house stimuli that differed in either the spatial distance among parts (configuration) or the shape of the parts. The FFA showed a much higher response to faces than to houses, but no preference for the configuration task over the part task. Similarly, the behavioral inversion effect was as large in the part task as the configuration task for faces, but absent in both part and configuration tasks for houses. These findings indicate that face perception mechanisms are not process specific for parts or configuration but are domain specific for face stimuli per se.

Brain↗

Numerical magnitude in the human parietal lobe; tests of representational generality and domain specificity.

Behavioral evidence suggests that human adults have a single system for representing the numerical magnitude of both symbolic numbers (e.g., Arabic digits) and nonsymbolic number stimuli (e.g., dot arrays). Brain imaging studies have implicated a specific parietal region in symbolic number processing, leading to the influential hypothesis that this region is the locus of a dedicated, domain-specific number system. Here we evaluated a prediction of this hypothesis, that this region should be activated not only by symbolic but also nonsymbolic number processing. Using nonsymbolic stimuli, we tested for higher parietal activations for number than for nonnumber comparison tasks (experiment 1), fMRI adaptation for numerosity repetition (experiment 2), and greater fMRI increases with increasing task difficulty for number than nonnumber tasks (experiment 3). None of these predictions were supported by the data, posing a serious challenge to the hypothesis that a single, domain-specific parietal region underlies both symbolic and nonsymbolic number representation.

Brain Mapping↗

The M170 is selective for faces, not for expertise.

Are the mechanisms for face perception selectively involved in processing faces per se, or do they also participate in the processing of any class of visual stimuli that share the same basic configuration and for which the observer has gained substantial visual expertise? Here we tested the effects of visual expertise on the face-selective "M170", a magnetoencephalography (MEG) response component that occurs 170 ms after stimulus onset and is involved in the identification of individual faces. In Experiment 1, cars did not elicit a higher M170 response (relative to control objects) in car experts compared to controls subjects. In Experiment 2, the M170 amplitude was correlated with successful face identification, but not with successful car identification in car experts. These results indicate that the early face processing mechanisms marked by the M170 are involved in the identification of faces in particular, not in the identification of any objects of expertise.

Adult↗

The fusiform face area subserves face perception, not generic within-category identification.

The function of the fusiform face area (FFA), a face-selective region in human extrastriate cortex, is a matter of active debate. Here we measured the correlation between FFA activity measured by functional magnetic resonance imaging (fMRI) and behavioral outcomes in perceptual tasks to determine the role of the FFA in the detection and within-category identification of faces and objects. Our data show that FFA activation is correlated on a trial-by-trial basis with both detecting the presence of faces and identifying specific faces. However, for most non-face objects (including cars seen by car experts), within-category identification performance was correlated with activation in other regions of the ventral occipitotemporal cortex, not the FFA. These results indicate that the FFA is involved in both detection and identification of faces, but that it has little involvement in within-category identification of non-face objects (including objects of expertise).

Adult↗

Functional magnetic resonance imaging provides new constraints on theories of the psychological refractory period.

We used functional magnetic resonance imaging (fMRI) to investigate the psychological refractory period (PRP), the delay in the response to the second of two tasks occurring in immediate succession. Our results were consistent with prior work on the PRP in that when two visual-manual tasks were presented within 100 ms of each other, the second response was delayed on the order of 500 ms, compared with when the two tasks were separated by 1,500 ms. Surprisingly, in brain regions postulated to be important for executive functions, there was virtually no increase in brain activation in the short-interval compared with the long-interval condition. These data suggest that passive queuing, rather than active monitoring, occurs during the PRP.

Adolescent↗

Common neural substrates for response selection across modalities and mapping paradigms.

In many situations, people can only compute one stimulus-to-response mapping at a time, suggesting that response selection constitutes a "central processing bottleneck" in human information processing. Using fMRI, we tested whether common or distinct brain regions were involved in response selection across visual and auditory inputs, and across spatial and nonspatial mapping rules. We isolated brain regions involved in response selection by comparing two conditions that were identical in perceptual input and motor output, but differed in the complexity of the mapping rule. In the visual-manual task of Experiment 1, four vertical lines were positioned from left to right, and subjects pressed one of four keys to report which line was unique in length. In the auditory-manual task of Experiment 2, four tones were presented in succession, and subjects pressed one of four keys to report which tone was unique in duration. For both visual and auditory tasks, the mapping between target position and key position was either spatially compatible or incompatible. In the verbal task of Experiment 3, subjects used nonspatial mappings that were either compatible ("same" if colors matched; "different" if they mismatched) or incompatible (the opposite). Extensive activation overlap was observed across all three experiments for incompatible versus compatible mapping in bilateral parietal and frontal regions. Our results indicate that common neural substrates are involved in response selection across input modalities and across spatial and nonspatial domains of stimulus-to-response mapping, consistent with behavioral evidence that response selection is a central process.

Acoustic Stimulation↗

Common neural mechanisms for response selection and perceptual processing.

Behavioral evidence supports a dissociation between response selection (RS; stimulus-to-response [S-R] mapping) and perceptual discrimination (PD): The former may be subject to a central processing bottleneck, whereas the latter is not (Pashler, 1994). We previously (Jiang & Kanwisher, 2003) identified a set of frontal and parietal regions involved in RS as those that produce a stronger signal when subjects follow a difficult S-R mapping rule than an easy mapping rule. Here, we test whether any of these regions are selectively activated by RS and not perceptual processing, as predicted by the central bottleneck view. In Experiment 1, subjects indicated which of four parallel lines was unique in length; PD was indexed by a higher BOLD response when the discrimination was difficult versus easy. Stimuli and responses were closely matched across conditions. We found that all regions-of-interest (ROIs) engaged by RS were also engaged by perceptual processing, arguing against the existence of mechanisms exclusively involved in RS. In Experiments 2 and 3, we asked what processes might go on in these ROIs, such that they could be recruited by both RS and perceptual processing. Our data argue against an account of this common activation in terms of spatial processing or general task difficulty. Thus, PD may recruit the same central processes that are engaged by RS.

Adult↗

The construction of large number representations in adults.

What is the nature of our mental representation of quantity? We find that human adults show no performance cost of comparing numerosities across vs. within visual and auditory stimulus sets, or across vs. within simultaneous and sequential sets. In addition, reaction time and performance in such tasks are determined by the ratio of the numerosities to be compared; absolute set size has no effect. These findings suggest that modality-specific stimulus properties undergo a non-iterative transformation into representations of quantity that are independent of the modality or format of the stimulus.

Adolescent↗

How distributed is visual category information in human occipito-temporal cortex? An fMRI study.

We used fMRI to study the distribution of object category information in the ventral visual pathway. Extending the findings of, we find that categories of stimuli can be distinguished by the pattern of activation they elicit across this entire pathway, even when the stimuli within a category differ in viewpoint, exemplar, or image format. However, regions within the ventral visual pathway are neither interchangeable nor equipotential. Although the FFA and PPA permit excellent discrimination between preferred versus nonpreferred stimuli (e.g., faces-bottles and houses-bottles, respectively), we find that neither region alone permits accurate discrimination between pairs of nonpreferred stimuli (e.g., bottles-shoes). These findings indicate that the ventral visual pathway is not homogeneous, but contains some regions (including FFA and PPA) that are primarily involved in the analysis of a single class of stimulus.

Evoked Potentials, Visual↗

Stages of processing in face perception: an MEG study.

Here we used magnetoencephalography (MEG) to investigate stages of processing in face perception in humans. We found a face-selective MEG response occurring only 100 ms after stimulus onset (the 'M100'), 70 ms earlier than previously reported. Further, the amplitude of this M100 response was correlated with successful categorization of stimuli as faces, but not with successful recognition of individual faces, whereas the previously-described face-selective 'M170' response was correlated with both processes. These data suggest that face processing proceeds through two stages: an initial stage of face categorization, and a later stage at which the identity of the individual face is extracted.

Adolescent↗

Covert orienting to the locations of targets and distractors: effects on response channel activation in a flanker task.

The role of covert orienting of attention in response channel activation was examined using the flanker interference and precueing paradigms. Four experiments assessed the influence of distractors on the discrimination of a target colour patch undercueing conditions (three with noninformative, exogenous cues and one with informative, endogenous cues) that modulated attention at the flanker or target locations. Across all of the experiments, the amount of interference generated by the distractors was not modulated by the facilitation and inhibition of return induced by spatial attention precues. These results are consistent with previous reports of patients with neglect, which demonstrated that flanker interference proceeds at unattended locations (Audet, Bub, & Lecours, 1991; Cohen, Ivry, Rafal, & Kohn, 1995), and they suggest that response channel activation can occur independently from spatial attention.

Adolescent↗