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Victor A F Lamme

Publications and source records attributed to Victor A F Lamme.

At least 19 recordsLinked to original sources

Towards a true neural stance on consciousness.

Consciousness is traditionally defined in mental or psychological terms. In trying to find its neural basis, introspective or behavioral observations are considered the gold standard, to which neural measures should be fitted. I argue that this poses serious problems for understanding the mind-brain relationship. To solve these problems, neural and behavioral measures should be put on an equal footing. I illustrate this by an example from visual neuroscience, in which both neural and behavioral arguments converge towards a coherent scientific definition of visual consciousness. However, to accept this definition, we need to let go of our intuitive or psychological notions of conscious experience and let the neuroscience arguments have their way. Only by moving our notion of mind towards that of brain can progress be made.

Attention↗

Strength of figure-ground activity in monkey primary visual cortex predicts saccadic reaction time in a delayed detection task.

When and where are decisions made? In the visual system a saccade, which is a fast shift of gaze toward a target in the visual scene, is the behavioral outcome of a decision. Current neurophysiological data and reaction time models show that saccadic reaction times are determined by a build-up of activity in motor-related structures, such as the frontal eye fields. These structures depend on the sensory evidence of the stimulus. Here we use a delayed figure-ground detection task to show that late modulated activity in the visual cortex (V1) predicts saccadic reaction time. This predictive activity is part of the process of figure-ground segregation and is specific for the saccade target location. These observations indicate that sensory signals are directly involved in the decision of when and where to look.

Animals↗

Zap! Magnetic tricks on conscious and unconscious vision.

Blindsight, the remarkable capability to react to unseen visual stimuli, has thus far only been demonstrated in patients and monkeys with a lesion to primary visual cortex. A recent study by Boyer, Harrison and Ro demonstrates blindsight in normal human observers, using TMS to block visual processing. Combined with other work, this opens new vistas towards understanding mechanisms of conscious and unconscious vision.

Animals↗

The influence of inattention on the neural correlates of scene segmentation.

Numerous experiments show that people are unable to report about unattended information. It is also clear that there is extensive processing in the absence of attention. Here, we study, by using an 'inattentional blindness' paradigm while measuring BOLD responses or MEG to texture displays, to what level of scene segmentation visual information is processed when subjects are not capable of reporting that segregating textures were present. We presented non-segregating and occasionally segregating textures in two different conditions: 1. a condition where subjects were not informed about the presence of the segregating textures while at the same time engaged in a foveal task, resulting in prolonged inattentional blindness and 2. a condition with similar task demands, in which, however, the subjects perceived the segregating textures. BOLD responses from early visual areas (V1, V2, V3, V4) and MEG responses up to 240 ms showed a significant difference between segregating and not segregating textures in both conditions and did not differ from each other, indicating that scene segmentation processes proceed normally during inattention. A difference between the two conditions, and hence an influence of attention, was signaled in area V3a and more parietal MEG sensors around 400 ms.

Adult↗

Figure-ground segregation requires two distinct periods of activity in V1: a transcranial magnetic stimulation study.

Discriminating objects from their surroundings by the visual system is known as figure-ground segregation. This process entails two different subprocesses: boundary detection and subsequent surface segregation or 'filling in'. In this study, we used transcranial magnetic stimulation to test the hypothesis that temporally distinct processes in V1 and related early visual areas such as V2 or V3 are causally related to the process of figure-ground segregation. Our results indicate that correct discrimination between two visual stimuli, which relies on figure-ground segregation, requires two separate periods of information processing in the early visual cortex: one around 130-160 ms and the other around 250-280 ms.

Adult↗

Repression of unconscious information by conscious processing: evidence from affective blindsight induced by transcranial magnetic stimulation.

Some patients with a lesion to the primary visual cortex (V1) show "blindsight": the remarkable ability to guess correctly about attributes of stimuli presented to the blind hemifield. Here, we show that blindsight can be induced in normal observers by using transcranial magnetic stimulation of the occipital cortex but exclusively for the affective content of unseen stimuli. Surprisingly, access to the affective content of stimuli disappears upon prolonged task training or when stimulus visibility increases, allegedly increasing the subjects' confidence in their overall performance. This finding suggests that availability of conscious information suppresses access to unconscious information, supporting the idea of consciousness as a repressant of unconscious tendencies.

Adult↗

Synchrony dynamics in monkey V1 predict success in visual detection.

Behavioral measures such as expectancy and attention have been associated with the strength of synchronous neural activity. On this basis, it is hypothesized that synchronous activity affects our ability to detect and recognize visual objects. To investigate the role of synchronous activity in visual perception, we studied the magnitude and precision of correlated activity, before and after stimulus presentation within the visual cortex (V1), in relation to a monkey's performance in a figure-ground discrimination task. We show that during the period of stimulus presentation a transition in synchronized activity occurs that is characterized by a reduction of the correlation peak height and width. Before stimulus onset, broad peak correlations are observed that change towards thin peak correlations after stimulus onset, due to a specific decrease of low-frequency components. The magnitude of the transition in correlated activity is larger, i.e. a stronger desynchronization occurs, when the animal perceives the stimulus correctly than when the animal fails to detect the stimulus. These results therefore show that a transition in synchronous firing is important for the detection of sensory stimuli. We hypothesize that the transition in synchrony reflects a change from loose and global neuronal interactions towards a finer temporal and spatial scale of neuronal interactions, and that such a change in neuronal interactions is required for figure-ground discrimination.

Animals↗

Relationship between change detection and pre-change [corrected] activity in visual area V1.

Humans are poor at detecting changes to visual scenes occurring during brief disruptions. It is unclear whether this 'change blindness' results from failure to process the relevant item before the change, or failure to compare/recall the item after the change. We recorded pre-change multi-unit activity in area V1 of monkeys performing a change detection task. The animals were rewarded for making a saccade to the changing figure. Figure-ground related activity was observed, even when no correct saccade was made. However, for the changing figure, pre-change activity was stronger in correct trials than in incorrect trials. We conclude that small differences in pre-change figure-ground segregation have predictive value in whether the change will be successfully detected.

Animals↗

Synchrony and covariation of firing rates in the primary visual cortex during contour grouping.

The visual system imposes structure onto incoming information, by grouping image elements of a single object together, and by segregating them from elements that belong to other objects and the background. One influential theory holds that the code for grouping and segmentation is carried by the synchrony of neuronal discharges on a millisecond time scale. We tested this theory by recording neuronal activity in the primary visual cortex (area V1) of monkeys engaged in a contour-grouping task. We found that synchrony was unrelated to contour grouping. The firing rates of V1 neurons are also correlated across trials. We demonstrate that this rate covariation is mainly determined by fluctuations in visual attention. Moreover, we show that rate covariation depends on perceptual grouping, as it is strongest between neurons that respond to features of the same object.

Animals↗

Correspondence of presaccadic activity in the monkey primary visual cortex with saccadic eye movements.

We continuously scan the visual world via rapid or saccadic eye movements. Such eye movements are guided by visual information, and thus the oculomotor structures that determine when and where to look need visual information to control the eye movements. To know whether visual areas contain activity that may contribute to the control of eye movements, we recorded neural responses in the visual cortex of monkeys engaged in a delayed figure-ground detection task and analyzed the activity during the period of oculomotor preparation. We show that approximately 100 ms before the onset of visually and memory-guided saccades neural activity in V1 becomes stronger where the strongest presaccadic responses are found at the location of the saccade target. In addition, in memory-guided saccades the strength of presaccadic activity shows a correlation with the onset of the saccade. These findings indicate that the primary visual cortex contains saccade-related responses and participates in visually guided oculomotor behavior.

Animals↗

The role of figure-ground segregation in change blindness.

Partial report methods have shown that a large-capacity representation exists for a few hundred milliseconds after a picture has disappeared. However, change blindness studies indicate that very limited information remains available when a changed version of the image is presented subsequently. What happens to the large-capacity representation? New input after the first image may interfere, but this is likely to depend on the characteristics of the new input. In our first experiment, we show that a display containing homogeneous image elements between changing images does not render the large-capacity representation unavailable. Interference occurs when these new elements define objects. On that basis we introduce a new method to produce change blindness: The second experiment shows that change blindness can be induced by redefining figure and background, without an interval between the displays. The local features (line segments) that defined figures and background were swapped, while the contours of the figures remained where they were. Normally, changes are easily detected when there is no interval. However, our paradigm results in massive change blindness. We propose that in a change blindness experiment, there is a large-capacity representation of the original image when it is followed by a homogeneous interval display, but that change blindness occurs whenever the changed image forces resegregation of figures from the background.

Cues↗

Set size effects in the macaque striate cortex.

Attentive processing is often described as a competition for resources among stimuli by mutual suppression. This is supported by findings that activity in extrastriate cortex is suppressed when several stimuli are presented simultaneously, compared to a single stimulus. In this study, we randomly varied the number of simultaneously presented figures (set size) in an attention-demanding change detection task, while we recorded multiunit activity in striate cortex (V1) in monkeys. After figure-background segregation, activity was suppressed as set size increased. This effect was stronger and started earlier among cells stimulated by the background than those stimulated by the figures themselves. As a consequence, contextual modulation, a correlate of figure-background segregation, increased with set size, approximately 100 msec after its initial generation. The results indicate that suppression of responses under increasing attentional demands differentially affects figure and background responses in area V1.

Animals↗

Figure-ground activity in primary visual cortex (V1) of the monkey matches the speed of behavioral response.

To look at an object its position in the visual scene has to be localized and subsequently appropriate oculo-motor behavior needs to be initiated. This kind of behavior is largely controlled by the cortical executive system, such as the frontal eye field. In this report, we analyzed neural activity in the visual cortex in relation to oculo-motor behavior. We show that in a figure-ground detection task, the strength of late modulated activity in the primary visual cortex correlates with the saccade latency. We propose that this may indicate that the variability of reaction times in the detection of a visual stimulus is reflected in low-level visual areas as well as in high-level areas.

Animals↗

Internal state of monkey primary visual cortex (V1) predicts figure-ground perception.

When stimulus information enters the visual cortex, it is rapidly processed for identification. However, sometimes the processing of the stimulus is inadequate and the subject fails to notice the stimulus. Human psychophysical studies show that this occurs during states of inattention or absent-mindedness. At a neurophysiological level, it remains unclear what these states are. To study the role of cortical state in perception, we analyzed neural activity in the monkey primary visual cortex before the appearance of a stimulus. We show that, before the appearance of a reported stimulus, neural activity was stronger and more correlated than for a not-reported stimulus. This indicates that the strength of neural activity and the functional connectivity between neurons in the primary visual cortex participate in the perceptual processing of stimulus information. Thus, to detect a stimulus, the visual cortex needs to be in an appropriate state.

Animals↗

Large capacity storage of integrated objects before change blindness.

Normal people have a strikingly low ability to detect changes in a visual scene. This has been taken as evidence that the brain represents only a few objects at a time, namely those currently in the focus of attention. In the present study, subjects were asked to detect changes in the orientation of rectangular figures in a textured display across a 1600 ms gray interval. In the first experiment, change detection improved when the location of a possible change was cued during the interval. The cue remained effective during the entire interval, but after the interval, it was ineffective, suggesting that an initially large representation was overwritten by the post-change display. To control for an effect of light intensity during the interval on the decay of the representation, we compared performance with a gray or a white interval screen in a second experiment. We found no difference between these conditions. In the third experiment, attention was occasionally misdirected during the interval by first cueing the wrong figure, before cueing the correct figure. This did not compromise performance compared to a single cue, indicating that when an item is attentionally selected, the representation of yet unchosen items remains available. In the fourth experiment, the cue was shown to be effective when changes in figure size and orientation were randomly mixed. At the time the cue appeared, subjects could not know whether size or orientation would change, therefore these results suggest that the representation contains features in their 'bound' state. Together, these findings indicate that change blindness involves overwriting of a large capacity representation by the post-change display.

Attention↗

Masking interrupts figure-ground signals in V1.

In a backward masking paradigm, a target stimulus is rapidly (<100 msec) followed by a second stimulus. This typically results in a dramatic decrease in the visibility of the target stimulus. It has been shown that masking reduces responses in V1. It is not known, however, which process in V1 is affected by the mask. In the past, we have shown that in V1, modulations of neural activity that are specifically related to figure-ground segregation can be recorded. Here, we recorded from awake macaque monkeys, engaged in a task where they had to detect figures from background in a pattern backward masking paradigm. We show that the V1 figure-ground signals are selectively and fully suppressed at target-mask intervals that psychophysically result in the target being invisible. Initial response transients, signalling the features that make up the scene, are not affected. As figure-ground modulations depend on feedback from extrastriate areas, these results suggest that masking selectively interrupts the recurrent interactions between V1 and higher visual areas.

Animals↗