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Visual Target (visual + target)
Selected AbstractsThe n -back as a dual-task: P300 morphology under divided attentionPSYCHOPHYSIOLOGY, Issue 6 2001Scott Watter The n -back task was hypothesized to be a dual task, permitting the imposition of parametrically increasing attentional and working memory demands, while keeping constant the demands of an embedded matching subtask. Visual targets were presented for 200 ms every 2.2 s at pseudorandomly varying positions on a computer screen. Participants were required to remember the most recent 0, 1, 2, or 3 positions and responded with a choice button push to whether the current target position matched the position presented n items previously. P300 peak latency was constant across n -back tasks, reflecting constant perceptual and cognitive demands of the matching subtask. P300 peak amplitude decreased with increasing memory load, reflecting reallocation of attention and processing capacity away from the matching subtask to working memory activity. These data support a dual-task nature of the n -back, which should be considered when employing this paradigm. [source] The strength of anticipatory spatial biasing predicts target discrimination at attended locations: a high-density EEG studyEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 11 2009Simon P. Kelly Abstract Cueing relevant spatial locations in advance of a visual target results in modulated processing of that target as a consequence of anticipatory attentional deployment, the neural signatures of which remain to be fully elucidated. A set of electrophysiological processes has been established as candidate markers of the invocation and maintenance of attentional bias in humans. These include spatially-selective event-related potential (ERP) components over the lateral parietal (around 200,300 ms post-cue), frontal (300,500 ms) and ventral visual (> 500 ms) cortex, as well as oscillatory amplitude changes in the alpha band (8,14 Hz). Here, we interrogated the roles played by these anticipatory processes in attentional orienting by testing for links with subsequent behavioral performance. We found that both target discriminability (d') and reaction times were significantly predicted on a trial-by-trial basis by lateralization of alpha-band amplitude in the 500 ms preceding the target, with improved speed and accuracy resulting from a greater relative decrease in alpha over the contralateral visual cortex. Reaction time was also predicted by a late posterior contralateral positivity in the broad-band ERP in the same time period, but this did not influence d'. In a further analysis we sought to identify the control signals involved in generating the anticipatory bias, by testing earlier broad-band ERP amplitude for covariation with alpha lateralization. We found that stronger alpha biasing was associated with a greater bilateral frontal positivity at ,390 ms but not with differential amplitude across hemispheres in any time period. Thus, during the establishment of an anticipatory spatial bias, while the expected target location is strongly encoded in lateralized activity in parietal and frontal areas, a distinct non-spatial control process seems to regulate the strength of the bias. [source] Reduced saccadic resilience and impaired saccadic adaptation due to cerebellar diseaseEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 1 2008Heidrun Golla Abstract The term short-term saccadic adaptation (STSA) captures our ability to unconsciously move the endpoint of a saccade to the final position of a visual target that has jumped to a new location during the saccade. STSA depends on the integrity of the cerebellar vermis. We tested the hypothesis that STSA reflects the working of a cerebellar mechanism needed to avoid ,fatigue', a gradual drop in saccade amplitude during a long series of stereotypic saccades. To this end we compared the kinematics of saccades of 14 patients suffering from different forms of cerebellar disease with those of controls in two tests of STSA and a test of saccadic resilience. Controls showed an increase in saccade amplitude (SA) for outward adaptation, prompted by outward target shifts, due to an increase in saccade duration (SD) in the face of constant peak velocity (PV). The decrease in SA due to inward adaptation was, contrariwise, accompanied by a drop in PV and SD. Whereas patients with intact vermis did not differ from controls, those with vermal pathology lacked outward adaptation: SD remained constant, as did SA and PV. In contrast, vermal patients demonstrated a significant decrease in SA, paralleled by a decrease in PV but mostly unaltered SD in the inward adaptation experiment as well as in the resilience test. These findings support the notion that inward adaptation is at least partially based on uncompensated fatigue. On the other hand, outward adaptation reflects an active mechanism for the compensation of fatigue, residing in the cerebellum. [source] Cortical mechanisms of smooth pursuit eye movements with target blanking.EUROPEAN JOURNAL OF NEUROSCIENCE, Issue 5 2004An fMRI study Abstract Smooth pursuit eye movements are evoked by retinal image motion of visible moving objects and can also be driven by the internal representation of a target due to extraretinal mechanisms (e.g. efference copy). To delineate the corresponding neuronal correlates, functional magnetic resonance imaging at 1.5 T was applied during smooth pursuit at 10 °/s with continuous target presentation and target blanking for 1 s to 16 right-handed healthy males. Eye movements were assessed during scanning sessions by infra-red reflection oculography. Smooth pursuit performance was optimal when the target was visible but decreased to a residual velocity of about 30% of the velocity observed during continuous target presentation. Random effects analysis of the imaging data yielded an activation pattern for smooth pursuit in the absence of a visual target (in contrast to continuous target presentation) which included a number of cortical areas in which extraretinal information is available such as the frontal eye field, the superior parietal lobe, the anterior and the posterior intraparietal sulcus and the premotor cortex, and also the supplementary and the presupplementary eye field, the supramarginal gyrus, the dorsolateral prefrontal cortex, cerebellar areas and the basal ganglia. We suggest that cortical mechanisms such as prediction, visuo-spatial attention and transformation, multimodal visuomotor control and working memory are of special importance for maintaining smooth pursuit eye movements in the absence of a visible target. [source] What is special about the index finger?: The index finger advantage in manipulating reflexive attentional shift,JAPANESE PSYCHOLOGICAL RESEARCH, Issue 4 2009ATSUNORI ARIGA Abstract Pointing with the index finger is a universal behavior. However, the functional significance of indexical pointing has not been examined empirically. We examined the efficacy of various pointing gestures in evoking viewer's attentional shifts. After viewing the gesture cue, observers quickly reported the location of a visual target. With a short cue-target delay, reaction times were generally shorter for the target at the location where gesture cues pointed, but not with a long cue-target delay. Moreover, the indexical pointing gesture produced a significantly larger cueing effect than the other gestures. Our control experiments indicated that the index-finger advantage is tightly linked to the proper morphological shape (i.e. length and position of the index finger) of the indexical pointing and is not explained by the directional discriminability of the gesture. The visual system seems to use mechanisms that are partially independent of the directional discrimination of gestures, in order to quickly modulate the viewer's attention. [source] Impaired modulation of the vestibulo-ocular reflex in Huntington's diseaseMOVEMENT DISORDERS, Issue 1 2004BSc(Hons), Joanne Fielding BA Abstract The vestibulo-ocular reflex (VOR) stabilizes gaze during movement, in conjunction with other afferent information: visual, proprioceptive, and somaesthetic. The reflex can either be augmented or suppressed, depending on visual requirements, and undergoes long-term adaptation to compensate for physical changes in the subject. Importantly, over relatively short periods of time, the VOR should function consistently under the same circumstances. This study examines VOR function in patients with Huntington's disease (HD), with a view to investigating cortical influences on the reflex. Horizontal eye movements were recorded in 9 patients with HD and 7 normal subjects, using the scleral search coil technique, in response to high frequency, unpredictable head rotations imposed manually. To establish base VOR function, recordings were made in darkness, without instruction, before and after wearing ×2 magnifying lenses for a period of 2 hours to adapt the reflex. Recordings were also made before adaptation, while fixating a stationary visual target (VOR augmentation), and while fixating a target moving with the head (VOR suppression). Although results suggest that the VOR is preserved in HD, with relatively normal gain values and appropriate augmentation and suppression of the reflex with visual input, patients were unable to adapt the VOR to altered visual conditions. This represents a novel finding in HD and suggests that cortical structures compromised in HD exert influences on the long-term adaptation of the VOR. © 2003 Movement Disorder Society [source] Reaction time is not impaired by stimulation of the ventral-intermediate nucleus of the thalamus (Vim) in patients with tremorMOVEMENT DISORDERS, Issue 3 2002Didier Flament PhD Abstract We studied the effect of high-frequency electrical stimulation of the ventral-intermediate nucleus of the thalamus (Vim) in four patients implanted with chronic stimulators to determine whether this procedure adversely affects reaction time to a proprioceptive stimulus. Two patients had undergone this surgery for treatment of tremor resulting from Parkinson's disease insufficiently responsive to levodopa therapy and two patients for treatment of essential tremor. Reaction times to auditory, visual, cutaneous, and proprioceptive stimuli were tested in a simple motor task requiring flexion of the elbow joint to a visual target in response to each stimulus. Reaction times were tested postoperatively with and without the stimulator turned on. We found that reaction time for all stimulus modalities was not increased when the stimulator was turned on; in fact, reaction times were, on average, slightly shorter during stimulation, but this difference was not statistically significant. We conclude that transmission of somatosensory inputs, necessary for initiating voluntary movement, from the periphery to the cortex is not significantly impaired by stimulation of the ventral-intermediate nucleus of the thalamus in patients with pathological tremor. © 2002 Movement Disorder Society [source] Evidence of alarm pheromones in the venom of Polistes dominulus workers (Hymenoptera: Vespidae)PHYSIOLOGICAL ENTOMOLOGY, Issue 3 2006CLAUDIA BRUSCHINI Abstract The active and coordinating capacity of defending the nest is a key feature of social insects. The present study investigates the presence of alarm pheromones in the venom of workers of the social wasp, Polistes dominulus. Laboratory experiments were performed with caged colonies of P. dominulus using a wind tunnel apparatus to test the behavioural response of workers to venom released by other workers and to venom extracts. Contrary to that previously reported for European paper wasps, the present results show that the venom is the source of alarm pheromones. Field experiments combining a visual (black target) and a chemical stimulus (venom extract) were performed to test the effect of the venom on the reaction of colonies. Wasps leave the nest, land on the visual target and attack the target significantly more once exposed to venom extract plus target than to solvent plus target. This work shows that the venom of P. dominulus workers elicits an alarm response, reduces the threshold for attack and acts as an attractant on targets. These results using P. dominulus indicate that, in both American and European species, colony defence is based on the same features, suggesting that chemical alarm is a widespread trait in the genus Polistes. [source] Is there a role of visual cortex in spatial hearing?EUROPEAN JOURNAL OF NEUROSCIENCE, Issue 11 2004Ulrike Zimmer Abstract The integration of auditory and visual spatial information is an important prerequisite for accurate orientation in the environment. However, while visual spatial information is based on retinal coordinates, the auditory system receives information on sound location in relation to the head. Thus, any deviation of the eyes from a central position results in a divergence between the retinal visual and the head-centred auditory coordinates. It has been suggested that this divergence is compensated for by a neural coordinate transformation, using a signal of eye-in-head position. Using functional magnetic resonance imaging, we investigated which cortical areas of the human brain participate in such auditory,visual coordinate transformations. Sounds were produced with different interaural level differences, leading to left, right or central intracranial percepts, while subjects directed their gaze to visual targets presented to the left, to the right or straight ahead. When gaze was to the left or right, we found the primary visual cortex (V1/V2) activated in both hemispheres. The occipital activation did not occur with sound lateralization per se, but was found exclusively in combination with eccentric eye positions. This result suggests a relation of neural processing in the visual cortex and the transformation of auditory spatial coordinates responsible for maintaining the perceptual alignment of audition and vision with changes in gaze direction. [source] Independent on-line control of the two hands during bimanual reachingEUROPEAN JOURNAL OF NEUROSCIENCE, Issue 6 2004Jörn Diedrichsen Abstract Many studies on bimanual coordination have shown that people exhibit a preference for mirror-symmetric movements. We demonstrate that this constraint is absent when bimanual reaching movements are made to visual targets. We investigated the ability of humans to make on-line adjustments during such movements when one or both targets were displaced during the initial phase of the movements. Adjustments were as efficient during bimanual as unimanual movements, even when two adjustments had to be made simultaneously. When one target was displaced in the bimanual condition, the hand reaching to that target adjusted efficiently to the displacement. However, a small transient perturbation in the trajectory of the other hand was also observed. This perturbation was in the same direction as the displacement, rather than in mirror-symmetric direction. A control experiment demonstrated that these perturbations could be elicited by visual information alone, but that they were also influenced by whether an adjustment was required in the trajectory of the other hand. Our results demonstrate near independent control of the two arms during visually guided reaching. The subtle interference observed between the arms reflects interactions between target-related representations in visual coordinates rather than between movement-related representations in joint- or muscle-coordinates. [source] Mere presence of distractors: Another determining factor for the attentional blink1JAPANESE PSYCHOLOGICAL RESEARCH, Issue 3 2003Jun-Ichiro Kawahara Abstract: When two visual targets are presented in rapid succession, perception of the second target is deteriorated if the temporal lag between the two targets is short (0,300 ms). This ,attentional blink' (AB) phenomenon has been believed to occur only when the second target is followed by a backward mask or when there is a task switching between two targets. The present study revealed another determining factor for the occurrence of the AB, the presence or absence of a distractor stream. Five experiments examined the effect of possible confounding factors in the extant literature and suggested that the mere presence of a distractor stream affects the processing of targets even when the observers tried to ignore them, resulting in a processing delay. This effect is discussed in a model of AB deficit in terms of decay of the second target's representation. [source] Reductions in N-acetylaspartylglutamate and the 67 kDa form of glutamic acid decarboxylase immunoreactivities in the visual system of albino and pigmented rats after optic nerve transectionsTHE JOURNAL OF COMPARATIVE NEUROLOGY, Issue 3 2003John R. Moffett Abstract This study compares the immunohistochemical distributions of N-acetylaspartylglutamate (NAAG) and the large isoform of the ,-aminobutyric acid (GABA)-synthesizing enzyme glutamic acid decarboxylase (GAD67) in the visual system of albino and pigmented rats. Most retinal ganglion cells and their axons were strongly immunoreactive for NAAG, whereas GAD67 immunoreactivity was very sparse in these cells and projections. In retinorecipient zones, NAAG and GAD67 immunoreactivities occurred in distinct populations of neurons and in dense networks of strongly immunoreactive fibers and synapses. Dual-labeling immunohistochemistry indicated that principal neurons were stained for NAAG, whereas local interneurons were stained for GAD67. In contrast to the distribution observed in retinorecipient zones, most or all neurons were doubly stained for NAAG and GAD67 in the thalamic reticular nucleus. Ten days after unilateral optic nerve transection, NAAG-immunoreactive fibers and synapses were substantially reduced in all contralateral retinal terminal zones. The posttransection pattern of NAAG-immunoreactive synaptic loss demarcated the contralateral and ipsilateral divisions of the retinal projections. In addition, an apparent transynaptic reduction in GAD67 immunoreactivity was observed in some deafferented areas, such as the lateral geniculate. These findings suggest a complicated picture in which NAAG and GABA are segregated in distinct neuronal populations in primary visual targets, yet they are colocalized in neurons of the thalamic reticular nucleus. This is consistent with NAAG acting as a neurotransmitter release modulator that is coreleased with a variety of classical transmitters in specific neural pathways. J. Comp. Neurol. 458:221,239, 2003. © 2003 Wiley-Liss, Inc. [source] | |||||||||||||