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P De Weerd

Publications and source records attributed to P De Weerd.

At least 19 recordsLinked to original sources
PubMed2003

Cortical mechanisms for acquisition and performance of bimanual motor sequences.

We used functional magnetic resonance imaging to investigate the cortical mechanisms contributing to the acquisition and performance of a complex, bimanual motor sequence. To that aim, five subjects were trained on a difficult, asymmetrical finger opposition task. Their performance rate almost doubled in the course of training and approached the performance rate in an untrained, symmetrical finger opposition task. Before training, performance of the asymmetrical sequence was associated with activity in M1, premotor cortex, supplementary motor cortex, and parietal cortex. After training, performance of the asymmetrical sequence was associated mainly with activity in M1, and little activity outside M1 remained. The latter pattern of cortical activation resembled that observed during the execution of symmetrical sequences, which was unaffected by practice with the asymmetrical sequence. The activation pattern obtained with the symmetrical bimanual sequence was indistinguishable from the combined activation measured in contralateral hemispheres during unimanual control sequences. The data indicate that cortical regions previously implicated in the acquisition of difficult unimanual motor sequences also contribute to the acquisition of asymmetrical bimanual sequences. We found no evidence for an expansion of activity in M1 after acquisition of the asymmetrical sequence (while this has been reported after acquisition of unimanual sequences). In the context of existing literature, the data suggest that the acquisition of unimanual and bimanual motor sequences may rely on similar cortical mechanisms, but that the formation of long-term, procedural memories for the two types of sequences might at least in part depend on different mechanisms.

Adult↗
PubMed2001

Modulation of sensory suppression: implications for receptive field sizes in the human visual cortex.

Neurophysiological studies in monkeys show that when multiple visual stimuli appear simultaneously in the visual field, they are not processed independently, but rather interact in a mutually suppressive way. This suggests that multiple stimuli compete for neural representation. Consistent with this notion, we have previously found in humans that functional magnetic resonance imaging (fMRI) signals in V1 and ventral extrastriate areas V2, V4, and TEO are smaller for simultaneously presented (i.e., competing) stimuli than for the same stimuli presented sequentially (i.e., not competing). Here we report that suppressive interactions between stimuli are also present in dorsal extrastriate areas V3A and MT, and we compare these interactions to those in areas V1 through TEO. To exclude the possibility that the differences in responses to simultaneously and sequentially presented stimuli were due to differences in the number of transient onsets, we tested for suppressive interactions in area V4, in an experiment that held constant the number of transient onsets. We found that the fMRI response to a stimulus in the upper visual field was suppressed by the presence of nearby stimuli in the lower visual field. Further, we excluded the possibility that the greater fMRI responses to sequential compared with simultaneous presentations were due to exogeneous attentional cueing by having our subjects count T's or L's at fixation, an attentionally demanding task. Behavioral testing demonstrated that neither condition interfered with performance of the T/L task. Our previous findings suggested that suppressive interactions among nearby stimuli in areas V1 through TEO were scaled to the receptive field (RF) sizes of neurons in those areas. Here we tested this idea by parametrically varying the spatial separation among stimuli in the display. Display sizes ranged from 2 x 2 degrees to 7 x 7 degrees and were centered at 5.5 degrees eccentricity. Based on the effects of display size on the magnitude of suppressive interactions, we estimated that RF sizes at an eccentricity of 5.5 degrees were <2 degrees in V1, 2-4 degrees in V2, 4-6 degrees in V4, larger than 7 degrees (but still confined to a quadrant) in TEO, and larger than 6 degrees (confined to a quadrant) in V3A. These estimates of RF sizes in human visual cortex are strikingly similar to those measured in physiological mapping studies in the homologous visual areas in monkeys.

Adult↗
PubMed2000

Texture segregation in the human visual cortex: A functional MRI study.

The segregation of visual scenes based on contour information is a fundamental process of early vision. Contours can be defined by simple cues, such as luminance, as well as by more complex cues, such as texture. Single-cell recording studies in monkeys suggest that the neural processing of complex contours starts as early as primary visual cortex. Additionally, lesion studies in monkeys indicate an important contribution of higher order areas to these processes. Using functional MRI, we have investigated the level at which neural correlates of texture segregation can be found in the human visual cortex. Activity evoked by line textures, with and without texture-defined boundaries, was compared in five healthy subjects. Areas V1, V2/VP, V4, TEO, and V3A were activated by both kinds of line textures as compared with blank presentations. Textures with boundaries forming a checkerboard pattern, relative to uniform textures, evoked significantly more activity in areas V4, TEO, less reliably in V3A, but not in V1 or V2/VP. These results provide evidence that higher order areas with large receptive fields play an important role in the segregation of visual scenes based on texture-defined boundaries.

Adult↗
PubMed1999

Increased activity in human visual cortex during directed attention in the absence of visual stimulation.

When subjects direct attention to a particular location in a visual scene, responses in the visual cortex to stimuli presented at that location are enhanced, and the suppressive influences of nearby distractors are reduced. What is the top-down signal that modulates the response to an attended versus an unattended stimulus? Here, we demonstrate increased activity related to attention in the absence of visual stimulation in extrastriate cortex when subjects covertly directed attention to a peripheral location expecting the onset of visual stimuli. Frontal and parietal areas showed a stronger signal increase during this expectation than did visual areas. The increased activity in visual cortex in the absence of visual stimulation may reflect a top-down bias of neural signals in favor of the attended location, which derives from a fronto-parietal network.

Attention↗
PubMed1999

Loss of attentional stimulus selection after extrastriate cortical lesions in macaques.

Many objects in natural visual scenes compete for attention. To identify the neural mechanisms necessary for visual attention, we made restricted lesions, affecting different quadrants of the visual field but leaving one quadrant intact, in extrastriate cortical areas V4 and TEO of two monkeys. Monkeys were trained to discriminate the orientation of a target grating surrounded by distracters. As distracter contrast increased, performance deteriorated in quadrants affected by V4 and TEO lesions, but not in the normal quadrant. Performance in affected quadrants was restored by increasing the contrast of the target relative to distracters. Thus, without V4 and TEO, visual attention is 'captured' by strong stimuli, regardless of their behavioral relevance.

Animals↗
PubMed1998

Mechanisms of directed attention in the human extrastriate cortex as revealed by functional MRI.

A typical scene contains many different objects, but the capacity of the visual system to process multiple stimuli at a given time is limited. Thus, attentional mechanisms are required to select relevant objects from among the many objects competing for visual processing. Evidence from functional magnetic resonance imaging (MRI) in humans showed that when multiple stimuli are present simultaneously in the visual field, their cortical representations within the object recognition pathway interact in a competitive, suppressive fashion. Directing attention to one of the stimuli counteracts the suppressive influence of nearby stimuli. This mechanism may serve to filter out irrelevant information in cluttered visual scenes.

Adult↗
PubMed1998

Perceptual filling-in: a parametric study.

We studied perceptual filling-in during maintained peripheral viewing of a uniform gray or red figure presented on a large textured background. Changes in the figure's size, shape, and eccentricity caused variations in the time required for filling-in that could be predicted from the size of its cortical projection within early visual areas. The data suggest that the time which elapsed before the figure was filled-in by its background reflects the time required for figure-ground segregation to fail, rather than a slow spread of the background across the figure. Our findings reveal interactions between surface segregation and filling-in which may be at the basis of normal surface perception.

Figural Aftereffect↗
PubMed1996

Orientation discrimination in the cat: its cortical locus II. Extrastriate cortical areas.

Luminance-defined edges or bars are among the basic units of visual analysis: a "primitive" component of perception. We have utilized this stimulus in a psychophysical study of bar orientation discrimination in the cat before and after selective lesions in visual cortical areas. The cortices have been divided on the basis of their connectivity into three tiers. Tier I refers to areas 17 and 18, tier II includes areas that receive directly from tier I, and tier III includes those areas that receive directly from tier II. Previous studies (Vandenbussche et al. [1991] J. Comp. Neurol. 305:632-658) have shown that the discrimination of bar orientation depends heavily upon the integrity of areas 17 and 18 (tier I). The present study indicates that several extrastriate areas in tiers II and III contribute to this discrimination task. Our data suggest that the anterior medial lateral suprasylvian, the posterior lateral lateral suprasylvian (tier II), and the anterior lateral lateral suprasylvian (tier III) areas are most likely to contribute to bar orientation discrimination.

Animals↗
PubMed1995

Responses of cells in monkey visual cortex during perceptual filling-in of an artificial scotoma.

When we view a scene through one eye, we typically do not see the scotomas created by the optic disc and the blood vessels overlying the retinal surface. Similarly, when a texture field containing a hole is steadily viewed in peripheral vision (artificial scotoma), the hole appears to fill in with the surrounding texture in a matter of seconds, demonstrating that the visual system fills in information across regions where no information is available. Here we show that, in monkeys viewing a similar texture field with a hole, the responses of extrastriate visual neurons with receptive fields covering the hole increase gradually to a level comparable to that elicited by the same texture without a hole. The time course of these dynamic changes in activity parallels the time course of perceived filling-in of the hole by human observers, suggesting that this process mediates perceptual filling-in.

Animals↗
PubMed1994

Two stages in visual texture segregation: a lesion study in the cat.

We have used five cats to investigate the effects of two distinct visual cortex lesions on the segregation of two different texture stimuli. The ablation of areas 17 and 18 (tier I) severely impaired the segregation between textures made of line elements differing in orientation, but spared the segregation between annulus and dot textures. In contrast, the ablation of those areas receiving direct afferents from areas 17 and 18 (tier II) destroyed the segregation for both texture stimuli. Strong deficits remained up to 1 year after the lesion, although limited recovery was observed after tier II lesions. We suggest that tier I areas are involved in the local filtering of the texture elements, and that tier II areas compute texture differences on the basis of the filtered image provided by tier I areas. The crucial contribution to texture segregation of visual areas belonging to a second level in the cortical hierarchy challenges the notion that texture segregation is entirely an early process in vision.

Animals↗
PubMed1993

Effects of visual cortex lesions on orientation discrimination of illusory contours in the cat.

We have trained five cats in orientation discrimination using different contours, and compared the deficits caused by lesions of cortical areas 17 and 18 (tier I) to the deficits induced by removal of those areas receiving afferents originating in areas 17 and 18 (tier II). As contour stimuli we used two types of illusory contours and a luminance bar. The two illusory contours were defined by opposed line-ends. One of them coincided with a luminance gradient whereas the other did not. Tier I lesions destroyed the capacity to discriminate the orientation of both illusory contours, and also caused an important, though less severe, deficit in bar orientation discrimination. The deficits induced by tier I lesions were permanent. Tier II lesions also caused significant deficits in orientation discrimination of illusory contours, but only a negligible deficit in bar orientation discrimination, and this result was not a mere consequence of a difference in difficulty between the tasks involving bars and illusory contours. In addition, tier II lesions differentiated between illusory contour types, the deficit being more pronounced for the illusory contour without luminance gradient than for the one with luminance gradient. In contrast to tier I lesions, tier II lesions allowed significant recovery, leading to small final deficits for all contour types tested.

Animals↗
PubMed1993

Occlusion cues contribute to orientation judgments of occlusion-defined contours.

Occlusion cues defining a contour in a 2-D stimulus pattern were shown to contribute to the accuracy of orientation judgments of that contour. The stimulus pattern was altered so that the occlusion cues became ambiguous, by introducing a textured background suggesting transparency of the stimulus pattern. Orientation judgments then became significantly less accurate. This finding shows that occlusion cues in 2-D patterns can be behaviorally relevant, in addition to generating the subjective percept commonly known as an illusory contour. The disruptive effect of the textured background on orientation judgments remained when no texture elements were present in the vicinity of the contour. This suggests that the generation of occlusion-defined contours relies as much on an evaluation of the surfaces at either side of the contour as being opaque as it does on local encoding of occlusion cues close to the contour. Finally, orientation sensitivity measured with contours defined by other than occlusion cues was not altered after the introduction of a textured background.

Female↗
PubMed1992

Texture segregation in the cat: a parametric study.

We have investigated how different texture parameters affect texture segregation in the cat, and which strategies cats use to solve the segregation task. Five cats were presented with stimuli consisting of two adjacent panels. One side contained a square area of a particular texture embedded in a different background texture; the other side was filled with only the background texture. The animal's task was to detect at which side the texture difference was presented. Sensitivity for the texture difference was assessed by making one aspect of the texture (in most instances the size of the texture elements) dependent upon performance by means of a staircase procedure. Among the most prominent parametric effects are those of density and element position randomization. In general, segregation was optimal at intermediate densities and deteriorated at larger and smaller densities. Element position randomization caused a slight but systematic decrease in segregation performance. Furthermore, we found texture elements at the border between different textures to be of primary importance for segregation. Which strategy the animals used for solving the segregation task depended upon the presence of random figure/background reversals in subsequent stimulus presentations during training. The animals learned to detect texture differences if these reversals were present, and without reversals, they learned to identify the particular texture in the target square. Interestingly, parameter dependencies of segregation did not depend upon the detection strategy used. We have speculated that the two different strategies used by the cats to solve the segregation tasks are related to different hierarchical levels of texture segregation which can be traced back to different stages of texture processing in human models of segregation performance.

Animals↗
PubMed1992

Epitope regions on U1 small nuclear RNA recognized by anti-U1RNA-specific autoantibodies.

Autoantibodies specifically directed to U1RNA were found in patients suffering from systemic lupus erythematosus (SLE) overlap syndromes. To obtain more insight in the mechanism responsible for this U1RNA-specific antibody formation and to use the antibodies eventually as a tool to study U1RNA-protein (U1RNP) interactions, the B cell epitopes on U1RNA were mapped. Using in vitro synthesized domains of U1RNA, the main epitope regions were found in stemloops II and IV. Furthermore, 3'-end or 5'-end truncation of both stemloop II and stemloop IV showed that the conformation of the stemloops is critical for antibody recognition. Mutant studies on both stemloops indicated that in the case of stemloop II the stem is the main antigenic region, whereas in stemloop IV, the loop (E-loop) is a main target. The results of this study support the idea that the anti-U1RNA autoantibody could be the result of a process driven by the human U1RNP complex itself (antigen-driven process).

Antibody Affinity↗
PubMed1990

Staircase procedure and constant stimuli method in cat psychophysics.

We measured 73.5% correct just noticeable differences (JNDs) in bar orientation with the method of constant stimuli and with a Wetherill and Levitt staircase procedure, using a total of 25 cats. For the same number of trials per threshold assessment, the variability of the threshold remained independent of the testing method used. However, the JNDs measured using the method of constant stimuli were significantly influenced by the range of the orientation differences (ODs) utilized for measuring the JND. This effect was particularly large in incompletely trained cats, but it also was significant in extensively trained subjects. On the other hand, staircase threshold measurements were not affected by the starting OD, independently of how well the animals had been trained. This shows that the staircase procedure is a more efficient instrument with which to measure JNDs in orientation than is the method of constant stimuli. With the staircase procedure, we found that the JNDs measured at oblique reference orientations did not exceed those measured at principal reference orientations (no oblique effect). Two earlier studies from this laboratory using the method of constant stimuli did report an oblique effect. Our data suggest that this oblique effect might stem from a less efficient training at the right oblique reference orientation in these studies, combined with a relatively inefficient testing procedure such as the constant stimuli method.

Animals↗
PubMed1990

Illusory contour orientation discrimination in the cat.

We present the first evidence that a non-human species (the cat) is able to discriminate the orientation of illusory contours. Following Vogels and Orban45, we used two types of illusory contours. In one type, the illusory contour was defined by a number of contour-inducing semicircles, of which the endpoints were separated by a gap. In the other pattern, the inducing semicircles were shifted in phase along their diameter and their endpoints were aligned along the contour. Just noticeable differences in orientation were measured (at the 73.5% correct level), using a Wetherill and Levitt49 staircase procedure. Values in the order of 11 degrees were obtained when using the first type of illusory contour. Just noticeable differences with the second type were in the order of 17 degrees. Reducing the salience of the illusory contour, whether by scrambling the contour, or by decreasing the number or the contrast of inducing semicircles, systematically increased discrimination thresholds.

Animals↗
PubMed1990

Bar orientation discrimination in the cat.

We have measured orientation-discrimination thresholds of 4 deg in the cat, confirming an earlier study of Vandenbussche and Orban (1983). Unlike Vandenbussche and Orban (1983), we found that orientation-discrimination performance is not better at principal, as compared to oblique, reference orientations (no oblique effect). Despite the absence of the oblique effect, and despite the discrimination thresholds which were elevated by a factor of 4 compared to humans, orientation-discrimination performance of cats and humans is qualitatively similar in a number of aspects. First, orientation-discrimination performance as a function of length and contrast is qualitatively similar to human performance. Second, as in humans, detection and discrimination of the stimuli are closely related. Finally, randomizing the contrast between the stimuli does not affect orientation-discrimination performance. This suggests that similar computations underlay orientation-discrimination performance in both species. In summary, our results confirm that the cat is a useful model for human orientation-discrimination performance.

Animals↗