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Justin A Harris

Publications and source records attributed to Justin A Harris.

12 recordsLinked to original sources

Factors affecting frequency discrimination of vibrotactile stimuli: implications for cortical encoding.

BACKGROUND: Measuring perceptual judgments about stimuli while manipulating their physical characteristics can uncover the neural algorithms underlying sensory processing. We carried out psychophysical experiments to examine how humans discriminate vibrotactile stimuli. METHODOLOGY/PRINCIPAL FINDINGS: Subjects compared the frequencies of two sinusoidal vibrations applied sequentially to one fingertip. Performance was reduced when (1) the root mean square velocity (or energy) of the vibrations was equated by adjusting their amplitudes, and (2) the vibrations were noisy (their temporal structure was irregular). These effects were super-additive when subjects compared noisy vibrations that had equal velocity, indicating that frequency judgments became more dependent on the vibrations' temporal structure when differential information about velocity was eliminated. To investigate which areas of the somatosensory system use information about velocity and temporal structure, we required subjects to compare vibrations applied sequentially to opposite hands. This paradigm exploits the fact that tactile input to neurons at early levels (e.g., the primary somatosensory cortex, SI) is largely confined to the contralateral side of the body, so these neurons are less able to contribute to vibration comparisons between hands. The subjects' performance was still sensitive to differences in vibration velocity, but became less sensitive to noise. CONCLUSIONS/SIGNIFICANCE: We conclude that vibration frequency is represented in different ways by different mechanisms distributed across multiple cortical regions. Which mechanisms support the "readout" of frequency varies according to the information present in the vibration. Overall, the present findings are consistent with a model in which information about vibration velocity is coded in regions beyond SI. While adaptive processes within SI also contribute to the representation of frequency, this adaptation is influenced by the temporal regularity of the vibration.

Adolescent↗

Localization of tactile stimuli depends on conscious detection.

Neurological reports of "tactile blindsight" suggest that the human somatosensory system can extract behaviorally useful information about the location of a tactile stimulus in the absence of conscious awareness that the stimulus occurred (Paillard et al., 1983; Rossetti et al., 1995). However, in a series of psychophysical experiments with neurologically intact subjects, we found no evidence for such a dissociation. Our subjects' ability to name the finger on which a tactile stimulus had been presented was dependent on their ability to consciously detect that stimulus (Harris et al., 2004). The present experiments followed up on this study and specifically sought evidence for a dissociation when subjects were required to indicate the location of the stimulus either by pointing at or moving the stimulated finger, the same response made by the neurological patients. Once again, localization accuracy was correlated with detection, and, crucially, when both detection and localization were measured using equivalent forced-choice tasks, the subjects were completely unable to identify the location of stimuli that they had not detected. These findings are inconsistent with the dissociation implied by the cases of tactile blindsight, but are consistent with other neurological evidence that detection of a tactile stimulus does not depend on localization (Head and Holmes, 1911; Halligan et al., 1995; Rapp et al., 2002).

Adolescent↗

Elemental representations of stimuli in associative learning.

This article reviews evidence and theories concerning the nature of stimulus representations in Pavlovian conditioning. It focuses on the elemental approach developed in stimulus sampling theory (R. C. Atkinson & W. K. Estes, 1963; R. R. Bush & F. Mosteller, 1951b) and extended by I. P. L. McLaren and N. J. Mackintosh (2000, 2002) and contrasts this with models that invoke notions of configural representations that uniquely code for different patterns of stimulus inputs (e.g., J. M. Pearce, 1987, 1994; R. A. Rescorla & A. R. Wagner, 1972; A. R. Wagner & S. E. Brandon, 2001). The article then presents a new elemental model that emphasizes interactions between stimulus elements. This model is shown to explain a range of behavioral findings, including those (e.g., negative patterning and biconditional discriminations) traditionally thought to be beyond the explanatory capabilities of elemental models. Moreover, the model offers a ready explanation for recent findings reported by R. A. Rescorla (2000, 2001, 2002b) concerning the way that stimuli with different conditioning histories acquire associative strength when conditioned in compound.

Association Learning↗

Psychophysical investigations into cortical encoding of vibrotactile stimuli.

Neurons in primary somatosensory cortex (S1) respond to vibrotactile stimuli by firing in phase with each cycle of the vibration. We have investigated how neural activity in S1 might contribute to people's perception of vibration frequency. The contribution of S1 was confirmed using transcranial magnetic stimulation (TMS): accuracy in comparing the frequency of two sequential vibrations was reduced by a single TMS pulse delivered to S1 in the interval between the two vibrations. More recent experiments have revealed that participants use the velocity (or energy) of the stimulus when judging its frequency. This is consistent with a contribution from S1: electrophysiological recording in S1 cortex of rats shows that neurons in S1 do not explicitly code vibration frequency, but instead code the product of frequency and amplitude (proportional to the mean velocity or energy of the vibration). Further, frequency discrimination is reduced by the addition of even very small amounts of noise to the temporal structure of the vibrations (making them irregular). However, noise has no effect if the two vibrations are presented on opposite fingertips (i.e. beyond the range of receptive field sizes of neurons in S1), or if there is no difference in their velocity. Therefore, when judging vibration frequency, humans utilize information about stimulus velocity as coded by neurons in S1, but this coding is dependent on the temporally regular input of the vibration.

Animals↗

Contextual modulation outside of awareness.

Contextual effects are ubiquitous in vision and reveal fundamental principles of sensory coding. Here, we demonstrate that an oriented surround grating can affect the perceived orientation of a central test grating even when backward masking of the surround prevents its orientation from being consciously perceived. The effect survives introduction of a gap between test and surround of over a degree even under masking, suggesting either that contextual information can effectively propagate across early visual cortex in the absence of awareness of the signaled context or that it can proceed undetected to higher processing levels at which such horizontal propagation may not be necessary. The effect under masking also shows partial interocular transfer, demonstrating processing of orientation by binocular neurons in visual cortex in the absence of conscious orientation perception. This pattern of results is consistent with the suggestion that simultaneous orientation contrast is mediated at multiple levels of the visual processing hierarchy, and it supports the view that propagation of signals to and, possibly, back from higher visual areas is necessary for conscious perception.

Awareness↗

Interactions between conditioned and unconditioned flavor preferences.

Five experiments investigated how rats' conditioned preferences or aversions for aqueous odors paired with sucrose or salt are affected by their unconditioned response to those tastes. Rats preferred an odor paired with 30% sucrose over an odor paired with 5% sucrose when both were presented in 5% sucrose, but they showed no preference or, if thirsty, showed the reverse preference, when the odors were presented in 30% sucrose. These changes in conditioned preference corresponded to changes in the rats' unconditioned preference for the accompanying sucrose solution. Rats' conditioned aversions for odors paired with salt showed a similar dependence on their reaction to the accompanying salt solution. The results were interpreted as showing that conditioned and unconditioned flavor preferences combine additively, as if mediated by the same sensory representation.

Analysis of Variance↗

Dissociating detection from localization of tactile stimuli.

In what they described as "a tactile analog of blindsight," Paillard et al. (1983) reported the case of a woman with damage to the left parietal cortex who was profoundly impaired in detecting tactile stimuli but could nonetheless correctly identify their location (also Rossetti et al., 1995). This stands in direct contrast to reports of neurological patients who were unable to accurately locate stimuli that they could successfully detect (Head and Holmes, 1911; Halligan et al., 1995; Rapp et al., 2002). The combination of these findings suggests that detecting and locating tactile stimuli are doubly dissociable processes, presumably mediated by different neural structures. We conducted four psychophysical experiments seeking evidence for such a double dissociation in neurologically intact subjects. We compared people's accuracy in detecting versus locating a tactile stimulus presented to one of four fingers and followed by a vibrotactile mask presented to all four fingers. Accuracy scores for both the yes-no detection and four-alternative forced-choice location judgments were converted to a bias-free measure (d'), which revealed that subjects were better at detecting than locating the stimulus. Detection was also more sensitive than localization to manipulations involving the mask: detection accuracy increased more steeply than localization accuracy as the target-mask interval increased, and detection, but not localization, was affected by changes in the mask frequency. By comparing these results with simulated data generated by computational models, we conclude that detection and localization are not mutually independent as previous neurological studies might suggest, but rather localization is subsequent to detection in a serially organized sensory processing hierarchy.

Adolescent↗

Persistence of preference for a flavor presented in simultaneous compound with sucrose.

Rats exposed to a simultaneous compound of a flavor and sucrose subsequently exhibited a preference for the flavor over water. This preference persisted across repeated testing even though the flavor was presented in the absence of sucrose. The preference did, however, extinguish if the rats were hungry when trained or tested, or if they had been reexposed to sucrose between training and test. Though failing to extinguish the preference, presentation of the flavor outside the compound protected it from the effects of sucrose devaluation, indicating that these presentations extinguished the within-compound association between the flavor and sucrose. The authors conclude that the hedonic reaction elicited by sucrose imbues the flavor with the same hedonic properties, and these properties maintain the preference independently of the flavor-sucrose association.

Animals↗

Transient storage of a tactile memory trace in primary somatosensory cortex.

Working memory is known to involve prefrontal cortex and posterior regions of association cortex (e.g., the inferior temporal lobes). Here, we investigate the potential role of primary somatosensory cortex (SI) in a working memory task with tactile stimuli. Subjects were required to compare the frequencies of two vibrations separated by a retention interval of 1500 msec. Their performance was significantly disrupted when we delivered a pulse of transcranial magnetic stimulation (TMS) to the contralateral SI early (300 or 600 msec) in the retention interval. TMS did not affect tactile working memory if delivered to contralateral SI late in the retention interval (at 900 or 1200 msec), nor did TMS affect performance if delivered to the ipsilateral SI at any time point. Primary sensory cortex thus seems to act not only as a center for on-line sensory processing but also as a transient storage site for information that contributes to working memory.

Adult↗

Mental-rotation deficits following damage to the right basal ganglia.

The authors report the case of a woman with a right basal ganglia lesion and severe mental-rotation impairments. She had no difficulty recognizing rotated objects and had intact left-right orientation in egocentric space but was unable to map the left and right sides of external objects to her egocentric reference frame. This study indicates that the right basal ganglia may be critical components in a cortico-subcortical network involved in mental rotation. We speculate that the role of these structures is to select and maintain an appropriate motor program for performing smooth and accurate rotation. The results also have important implications for theories of object recognition by demonstrating that recognition of rotated objects can be achieved without mental rotation.

Aged↗

Reinstatement of fear to an extinguished conditioned stimulus: two roles for context.

The authors studied the role of context in reinstatement. Freezing was reinstated when the conditioned stimulus (CS) was extinguished in 1 context and rats moved to another context for reexposure to the shock unconditioned stimulus (US) and test. It was also reinstated (rather than renewed) when rats were shocked in the extinction context and moved to another context for test. This reinstatement was CS specific and reduced by nonreinforced exposures to the extinction context. Rats shocked in the context in which a stimulus had been preexposed froze when tested in another context. These findings suggest 2 roles for context in reinstatement: conditioning of the test context (M. E. Bouton, 1993) and mediated conditioning by the extinction context (P. C. Holland, 1990).

Animals↗

Investigations into the organization of information in sensory cortex.

One might take the exploration of sensory cortex in the first decades of the last century as the opening chapter of modern neuroscience. The combined approaches of (i) measuring effects of restricted ablation on functional capacities, both in the clinic and the laboratory, together with (ii) anatomical investigations of cortical lamination, arealization, and connectivity, and (iii) the early physiological probing of sensory representations, led to a fundamental body of knowledge that remains relevant to this day. In our time, there can be little doubt that its organization as a mosaic of columnar modules is the pervasive functional property of mammalian sensory cortex [Brain 120 (1997) 701]. If one accepts the assertion that columns and maps must improve the functioning of the brain (why else would they be the very hallmark of neocortex?), then the inevitable question is: exactly what advantages do they permit? In this review of our recent presentation at the workshop on Homeostasis, plasticity and learning at the Institut Henri Poincaré, we will outline a systematic approach to investigating the role of modular, map-like cortical organization in the processing of sensory information. We survey current evidence concerning the functional significance of cortical maps and modules, arguing that sensory cortex is involved not solely in the online processing of afferent data, but also in the storage and retrieval of information. We also show that the topographic framework of primary sensory cortex renders the encoding of sensory information efficient, fast and reliable.

Animals↗