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E Hennighausen

Publications and source records attributed to E Hennighausen.

13 recordsLinked to original sources

Response preparation begins before mental rotation is finished: evidence from event-related brain potentials.

Behavioral data (response time (RT) and accuracy) and psychophysiological data (event-related brain potentials of ERPs, and lateralized readiness potential or LRP) were studied in an experiment in which rotated alphanumeric characters were presented normally or mirror-reversed. In half of the trials, character classification (letter versus digit) determined whether or not the response was to be executed (go versus nogo) and parity determined the responding hand. In the other half, classification determined the responding hand and parity determined go versus nogo. LRP data indicated that response preparation occurred before mental rotation was finished. These data contradict strictly sequential discrete models of information processing and suggest continuous flow of information.

Adult

Topography of brain electrical activity dissociates the retrieval of spatial versus verbal information from episodic long-term memory in humans.

Topography and amplitude of slow event-related potentials (ERPs) of the electroencephalogram (EEG) were studied during acquisition and recall of spatial and verbal associations. Subjects learned associations between line drawings and two types of mediators. The latter were either positions in a grid or concrete nouns. In a cued recall test subjects had to decide whether two drawings were linked to each other or not via an associated position or noun. The topography of slow ERPs 1-4 s after stimulus presentation obtained from 18 scalp electrodes dissociated the memory processes: The maximum potential was found over the parietal cortex with spatial and over the left frontal cortex with verbal information. The same topographic pattern emerged during both anticipation learning and cued recall. Moreover, the amplitude at the topographic maximum increased when more associations had to be retrieved. These results are compatible with the idea that memory representations are reactivated in localized cortical cell assemblies specialized for particular codes.

Adult

Different cortical activation patterns in blind and sighted humans during encoding and transformation of haptic images.

In this study, we investigated whether the occipital cortex of blind humans is activated during haptic perception and/or transformation of a haptic image. Slow event-related brain potentials were monitored from 18 electrodes in 12 sighted and 15 congenitally blind participants while they were engaged in a haptic mental rotation task. In both groups, slow negative shifts appeared over (a) the frontal cortex at the beginning of each processing episode, (b) the left-central to parietal cortex during encoding and maintaining of a haptic image, and (c) the central to parietal cortex during image transformation. A pronounced slow negative potential over the occipital cortex emerged only in the blind individuals and was time-locked to the processing epochs. Its amplitude increased with the amount of processing load. The slow wave effects observed in the blind individuals could indicate that occipital areas participate in specific, nonvisual functions or they could reflect a coactivation of these areas whenever the activation level of task-specific processing modules located elsewhere in the cortex is raised by nonspecific thalamocortical input.

Adult

[Memory traces in EEG].

The paper gives a brief overview of five experimental approaches in which memory processes were studied by means of event-related brain potentials (ERPs). Some of the results were already published in English (Study 1), while others are new and will be reported in greater length as full paper elsewhere (Studies 2, 3, 4, and 5). Study 1 revealed that retrieval of information from episodic long-term memory is accompanied by a systematic slow negative potential. The topography of this slow wave depends on the quality of the reactivated information (spatial vs. verbal), and its amplitude reflects the difficulty of the retrieval process. In experiment 2 ERPs were recorded while subjects acquired either explicit or implicit knowledge about a sequential stimulus-response pattern. The data suggest that explicit learners who posses verbalizable knowledge about sequential dependencies have formed both perceptual and motor representations, while implicit learners have formed motor representations only. In study 3 fact retrieval in mental arithmetic was activated by a verification task. Incongruent solutions evoked an arithmetic N400-effect whose amplitude varied with the associative distance between an expected and an actually perceived solution to a multiplication problem. In study 4 ERPs were recorded during mental rotation tasks. A set of experiments revealed that mental rotation is always accompanied by a systematic negative variation over the parietal cortex. The amplitude of this "rotation specific negativity" increases with an increasing angular disparity between a perceived sign and its normal upright template. It was shown that this negativity is functionally distinct from a P300-complex which is often superimposed on it within the same latency window. Finally, study 5 examined ERPs in a sentence reading task in which grammatically legal but infrequent sentence constructions had to be processed. A left-anterior negativity was observed whenever an explicit case marker (the definite article in German) signalled a nominal phrase at a noncanonical position. The LAN phenomenon appears to be a manifestation of a syntax processor which performes a first-pass formal analysis of a sentence and which possibly allocates working memory resources whenever a word cannot be assigned immediately to an expected propositional role.

Brain

Topographically distinct cortical activation in episodic long-term memory: the retrieval of spatial versus verbal information.

Two experiments are reported to study slow potentials in the EEG during reactivation of spatial and verbal information. Subjects had to learn associations between drawings and one, two, or three mediators (locations in Experiment 1, nouns in Experiment 2). During recall, subjects had to decide whether or not two drawings were linked to each other by a common mediator. EEG was recorded during learning and recall. Both experiments were completely equivalent. Irrespective of the quality of the mediators, response time proved to be a linear function of the numbers of mediators to be recalled. Negative slow potentials that accompanied the reactivation of information during anticipation learning and cued recall had a material-specific topography: The maximum was found over the parietal cortex for spatial information and over the left frontal cortex for verbal information. Moreover, the amplitude at these scalp locations varied with the amount of the to-be-retrieved information. The results support the claim of topographically distinct cell assemblies specialized for storage and retrieval of distinct kinds of information.

Adult

Event-related potentials during auditory and somatosensory discrimination in sighted and blind human subjects.

The objective of the present study was to test if and to what extent phasic and tonic event-related potentials of the human EEG may reflect phenomena of cortical plasticity. In particular, it was tested if the occipital cortex of blind subjects participates in the processing of non-visual stimuli. To this end, 12 blind and 12 blindfolded sighted subjects were tested in an auditory and a somatosensory discrimination task with 2 levels of discrimination difficulty. Slow and fast event-related potentials were recorded from 18 scalp electrodes. In addition to the negative slow waves found in sighted subjects over frontal and central sites during auditory and somatosensory discrimination, a pronounced negative wave was revealed in the blind also over occipital brain areas. These negative shifts were time-locked to the train of stimuli which had to be monitored with sustained attention, i.e. they rised and resolved with the beginning and the end of a 20-s discrimination time epoch. The P300 complex, on the other hand, which is a slow positive deflection over the posterior part of the scalp and which follows rare and task-relevant events 200-800 ms after stimulus onset was significantly smaller at occipital electrodes in the blind than in the sighted subjects. Combined with neurophysiological and neuronanatomical evidence originating from studies with visually deprived animals, these data suggest that the occipital cortex of blind human subjects is coactivated whenever the system is engaged in a task which requires sustained attention and is less effectively inhibited at the end of a perceptual time epoch. In total, the data cast doubt on the hypothesis that the occipital cortex of blind subjects participates in modality-specific non-visual information processing.

Adult

Exploring memory functions by means of brain electrical topography: a review.

A series of experiments is reviewed which explored whether the functional brain state of long-term memory retrieval is correlated with specific changes in slow, DC-like event-related brain potentials. The main results are: (1) Retrieving associations from long-term memory is accompanied by a slow negative shift of 5-10 microV which prevails about as long as the retrieval process lasts, i.e., in our experiments, for a period of several seconds: (2) When different types of representations have to be reactivated in memory the slow negative wave shows a clearly distinct topography. The maximum was found in a verbal condition over the left frontal, in a spatial condition over the parietal, and in a color condition over the right occipital to temporal cortex. All these conditions were completely equivalent with respect to the established associative structure, the learning procedure, and the performance criterion. (3) The amplitude of the topographic maximum increases with the number of representations which have to be reactivated. This effect is not due to a non-specific increase of effort but specifically related to the number of activated episodic memory contents which had been experimentally established. In contrast, the reactivation of a priori given semantic association did not become manifest in a specific slow wave effect. These findings are compatible with the idea that memory retrieval implies a reactivation of those cortical cell assemblies in the cortex in which the constituting features of a mnestic entity had originally been processed during perception and learning. The results are also discussed with respect to the possible advantages of EEG and MEG recordings for a cognitive psychophysiology in comparison to other brain imaging techniques as PET or fMRI.

Brain

Patterns of cerebral activation while mental images are rotated and changed in size.

Event-related brain potentials were recorded while subjects performed either a rotation or a size scaling transformation of a mental image. Images had to be rotated 0 degrees, 60 degrees, or 120 degrees or their size had to be enlarged by factors of 1:1, 1:3, or 1:5. Both tasks were accompanied by pronounced negative slow potentials, which extended over several seconds. The relative maximum of these shifts emerged at central to occipital leads. Over the occipital cortex, the negative potential had a similar amplitude level in all conditions and both tasks. However, at parietal and central areas, the negative slow wave changed in relation to the difficulty of the task. The amplitude increased with increasing rotation demands and if the scaling operation required an exact computation of the coordinates of the image. None of these effects could be attributed to an inverse change of P300.

Adult

Dynamics of activation in long-term memory: the retrieval of verbal, pictorial, spatial, and color information.

Paivio's (1986) dual code theory was tested in 5 experiments with a new paradigm for the FAN effect that enforced genuine memory recall. Subjects had to learn associations between concepts and mediators. The FAN of the concepts in relation to the mediators was varied systematically. Response times (RT) were measured while subjects had to decide whether 2 concepts were linked to each other or not by a common mediator. In Experiment 1 the concepts and mediators were words, whereas in the other experiments the concepts were line drawings. Colors served as mediators in Experiment 2 and spatial locations served as mediators in Experiments 3, 4, and 5. All of the experiments were equivalent with respect to the FAN, the learning procedure, and the retrieval test. In all of the experiments, RT proved to be a linear function of the FAN. These results suggested that the same dynamics hold for all types of information stored in long-term memory.

Adolescent

A correction method for DC drift artifacts.

In order to cope with the problem of drift artifacts in ERP research a new off-line correction method is described. It estimates the DC drift from all prestimulus baselines of an experiment. For this end, an amplifier reset is performed at regular intervals and the DC off-set preceding any reset is stored. A regression is calculated between the prestimulus baseline amplitudes of consecutive trials and the time that has passed by. The amplitude trend which can be explained by either a linear or non-linear regression model is then subtracted from all data points. The power of the method is illustrated by two examples. The first shows that detrending increases the signal-to-noise ratio in ANOVA designs. The second shows that amplitude differences of event-related slow potentials, which appeared between the first and the second half of an experiment, could be explained by a non-linear drift component.

Analysis of Variance

Topographic differences of slow event-related brain potentials in blind and sighted adult human subjects during haptic mental rotation.

Twelve blindfolded sighted, nine congenitally blind, and seven adventitiously blind subjects were tested in a haptic mental rotation task while slow event-related brain potentials in the EEG were recorded from 17 scalp locations. The overall topography of the slow wave pattern which prevailed during the task differed for sighted and for blind, but not for congenitally and adventitiously blind subjects. While the tactile stimuli were encoded, the blind showed a pronounced occipital and the sighted a pronounced frontal activation. The task-specific amplitude increment of a negative slow wave which can be understood as a manifestation of the process of mental rotation proper, showed a different topography for sighted and for blind subjects too. It had its maximum over central to parietal cortical areas in both groups, but it extended more towards occipital regions in the blind. In both groups, the effects were very similar to those observed in former studies with visual versions of the mental rotation task, i.e. the slow wave amplitude over central to parietal areas increased monotonously with an increasing angular disparity of the two stimuli to be compared. These results are discussed with respect to the question of whether visual deprivation in the blind can cause a reorganization of cortical representational maps.

Adult

Imagery-perception interaction depends on the shape of the image: a reply to Farah (1989).

Farah (1989) reported that point threshold stimuli are detected better if they appear at spatial locations in the visual field that are covered by an image. By replicating her experiment with 3 instead of the original 2 images, we found that the effect depends on the shape of the mentally projected image. A second experiment with 9 different shapes revealed that the effect is modulated by the compactness and the size of the image--it is enhanced with increasing compactness and attenuated with increasing size. These findings do not unequivocally support the idea that imagery and perception interact because both processes share the same representational medium. Rather, they suggest that imagery can cause a figure-ground segregation in the visual field and that the shape of the figure may determine the amount of attention that is allocated to different sections in the visual field.

Eidetic Imagery

[Haptic mental rotation in patients with congenital blindness, acquired blindness and normal vision persons].

Nineteen congenitally blind subjects (Ss), eleven Ss who went blind later in their life, and 42 control Ss with normal vision were tested in a tactile version of a "mental rotation" task. A specially constructed tactile display was used which enabled a rotation of the alphanumeric symbols in multiples of 60 degrees without any form distortion. Ss had to compare two successively presented symbols regarding whether the second was just a rotated version or also a mirror image of the first. Decision latencies and errors were recorded. Neither of dependent variables reveal any differences between the three groups of subjects. Moreover, the well known linear increase of decision latency as a function of angular disparity could also be observed with the tactile stimuli in all three groups. Both results are consistent with the assumption that mental rotation effects are neither linked to the visual modality nor to a manipulation of visual-analog representations. If the task is solved by so called analog processes then these seem to operate with non-visual spatial representations.

Adult