hosted by
publicationslist.org
    

Tanja Nijboer

Utrecht University
Experimental Psychology
Helmholtz Institute
Heidelberglaan 2
NL-3584 CS Utrecht
t.c.w.nijboer@uu.nl

Journal articles

2010
Tanja Nijboer, Anneloes Vree, Chris Dijkerman, Stefan Van der Stigchel (2010)  Prism adaptation influences perception but not attention: evidence from antisaccades.   Neuroreport 21: 5. 386-389 Mar  
Abstract: Prism adaptation has been shown to successfully alleviate symptoms of hemispatial neglect, yet the underlying mechanism is still poorly understood. In this study, the antisaccade task was used to measure the effects of prism adaptation on spatial attention in healthy participants. Results indicated that prism adaptation did not influence the saccade latencies or antisaccade errors, both strong measures of attentional deployment, despite a successful prism adaptation procedure. In contrast to visual attention, prism adaptation evoked a perceptual bias in visual space as measured by the landmark task. We conclude that prism adaptation has a differential influence on visual attention and visual perception in healthy participants as measured by the tasks used.
Notes:
Stefan Van der Stigchel, Tanja C W Nijboer (2010)  The imbalance of oculomotor capture in unilateral visual neglect.   Conscious Cogn 19: 1. 186-197 Mar  
Abstract: Visual neglect has been associated with an imbalance in the level of activity in the saccadic system: activity in the contralesional field is suppressed, which makes target selection unlikely. We recorded eye movements of a patient with hemispatial neglect and a group of healthy participants during an oculomotor distractor paradigm. Results showed that the interfering effects of a distractor were very strong when presented in her ipsilesional visual field. However, when the distractor was presented in her contralesional field, there were no interfering effects when the target was presented in her ipsilesional field. These findings could not be explained by the presence of a visual field defect as revealed by the results of two hemianopic patients. Our results are in line with an imbalance in the level of activity in the saccadic system in visual neglect because visual elements presented in the contralesional field did not compete for saccadic selection.
Notes:
2009
H C Dijkerman, R D McIntosh, I Schindler, T C W Nijboer, A D Milner (2009)  Choosing between alternative wrist postures: action planning needs perception.   Neuropsychologia 47: 6. 1476-1482 May  
Abstract: When normal subjects grasp with their right hand a rectangular object placed at different orientations in the horizontal plane, they change from a 'thumb left' (clockwise) to a 'thumb right' (anti-clockwise) grasp when the orientation exceeds about 110 degrees , with respect to the mid-sagittal plane. This suggests planning of the final grip orientation at, or before the start of the prehension movement. The current study assessed performance of two visual agnosic patients (SB and DF) on a grasping task requiring the planning of final grip posture. Five healthy subjects were also tested. Subjects were required to grasp a triangular-section block, which was presented at one of seven different orientations (80-140 degrees). The healthy subjects showed a consistent relation between object orientation and hand orientation just before contact. In addition, they consistently used a clockwise grasp when object orientation was less than 100 degrees , and an anti-clockwise grasp when it was more than 110 degrees, with a sharply defined switch-point being identifiable for each subject. For both visual agnosic patients, hand orientation was also reliably related to object orientation. However, the selection of grasp posture was markedly abnormal: they did not consistently switch between clockwise and anti-clockwise grasps within the normal orientation range, and the switch, when it did occur, was not at all sharply defined. These results suggest that the planning of hand orientation during a grasp depends on a perceptually based judgement of the awkwardness of alternative movements. This would presumably involve ventral stream processing, which is disrupted in the visual agnosic patients.
Notes:
Titia Gebuis, Tanja C W Nijboer, Maarten J van der Smagt (2009)  Of colored numbers and numbered colors: interactive processes in grapheme-color synesthesia.   Exp Psychol 56: 3. 180-187  
Abstract: Grapheme-color synesthetes experience a specific color when they see a grapheme but they do not report to perceive a grapheme when a color is presented. In this study, we investigate whether color can still evoke number-processes even when a vivid number experience is absent. We used color-number and number-color priming, both revealing faster responses in congruent compared to incongruent conditions. Interestingly, the congruency effect was of similar magnitude for both conditions, and a numerical distance effect was present only in the color-number priming task. In addition, a priming task in which synesthetes had to judge the parity of a colored number revealed faster responses in parity congruent than in parity incongruent trials. These combined results demonstrate that synesthesia is indeed bi-directional and of similar strength in both directions. Furthermore, they illustrate the precise nature of these interactions and show that the direction of these interactions is determined by task demands, not by the more vividly experienced aspect of the stimulus.
Notes:
Tanja C W Nijboer, Gudrun M S Nys, Maarten J van der Smagt, Edward H F de Haan (2009)  A selective deficit in the appreciation and recognition of brightness: brightness agnosia?   Cortex 45: 7. 816-824 Jul/Aug  
Abstract: We report a patient with extensive brain damage in the right hemisphere who demonstrated a severe impairment in the appreciation of brightness. Acuity, contrast sensitivity as well as luminance discrimination were normal, suggesting her brightness impairment is not a mere consequence of low-level sensory impairments. The patient was not able to indicate the darker or the lighter of two grey squares, even though she was able to see that they differed. In addition, she could not indicate whether the lights in a room were switched on or off, nor was she able to differentiate between normal greyscale images and inverted greyscale images. As the patient recognised objects, colours, and shapes correctly, the impairment is specific for brightness. As low-level, sensory processing is normal, this specific deficit in the recognition and appreciation of brightness appears to be of a higher, cognitive level, the level of semantic knowledge. This appears to be the first report of 'brightness agnosia'.
Notes:
Titia Gebuis, Tanja C W Nijboer, Maarten J Van der Smagt (2009)  Multiple dimensions in bi-directional synesthesia.   Eur J Neurosci 29: 8. 1703-1710 Apr  
Abstract: Grapheme-color synesthetes report seeing a specific color when a number is perceived. The reverse, the synesthetic experience of a specific grapheme after the percept of a color is extremely rare. However, recent studies have revealed these interactions at both behavioral and neurophysiological levels. We investigated whether similar neuronal processes (i.e. perceptual and/or attentional) may underlie this bi-directional interaction by measuring event-related potentials (ERPs) during both a number-color and color-number priming task. In addition, we investigated the unitarity of synesthesia by comparing two distinct subtypes of synesthetes, projectors and associators, and assessed whether consistencies between measures (i.e. behavioral and electrophysiological) were present across synesthetes. Our results show longer reaction times for incongruent compared with congruent trials in both tasks. This priming effect is also present in the P3b latency (parietal electrode site) and P3a amplitude (frontal electrode site) of the ERP data. Interestingly, projector and associator synesthetes did not reveal distinct behavioral or electrophysiological patterns. Instead, a dissociation was found when synesthetes were divided in two groups on the basis of their behavioral data. Synesthetes with a large behavioral priming effect revealed ERP modulation at the frontal and parietal electrode sites, whereas synesthetes with a small priming effect revealed a frontal effect only. Together, these results show, for the first time, that similar neural mechanisms underlie bi-directional synesthesia in synesthetes that do not report a synesthetic experience of a grapheme when a color is perceived. In addition, they add support for the notion of the existence of both 'lower' and 'higher' synesthetes.
Notes:
Tanja C W Nijboer, Stefan Van der Stigchel (2009)  Is attention essential for inducing synesthetic colors? Evidence from oculomotor distractors.   J Vis 9: 6. 21.1-21.9 06  
Abstract: In studies investigating visual attention in synesthesia, the targets usually induce a synesthetic color. To measure to what extent attention is necessary to induce synesthetic color experiences, one needs a task in which the synesthetic color is induced by a task-irrelevant distractor. In the current study, an oculomotor distractor task was used in which an eye movement was to be made to a physically colored target while ignoring a single physically colored or synesthetic distractor. Whereas many erroneous eye movements were made to distractors with an identical hue as the target (i.e., capture), much less interference was found with synesthetic distractors. The interference of synesthetic distractors was comparable with achromatic non-digit distractors. These results suggest that attention and hence overt recognition of the inducing stimulus are essential for the synesthetic color experience to occur.
Notes:
2008
R W Kentridge, T C W Nijboer, C A Heywood (2008)  Attended but unseen: visual attention is not sufficient for visual awareness.   Neuropsychologia 46: 3. 864-869 Feb  
Abstract: Does any one psychological process give rise to visual awareness? One candidate is selective attention-when we attend to something it seems we always see it. But if attention can selectively enhance our response to an unseen stimulus then attention cannot be a sufficient precondition for awareness. Kentridge, Heywood & Weiskrantz [Kentridge, R. W., Heywood, C. A., & Weiskrantz, L. (1999). Attention without awareness in blindsight. Proceedings of the Royal Society of London, Series B, 266, 1805-1811; Kentridge, R. W., Heywood, C. A., & Weiskrantz, L. (2004). Spatial attention speeds discrimination without awareness in blindsight. Neuropsychologia, 42, 831-835.] demonstrated just such a dissociation in the blindsight subject GY. Here, we test whether the dissociation generalizes to the normal population. We presented observers with pairs of coloured discs, each masked by the subsequent presentation of a coloured annulus. The discs acted as primes, speeding discrimination of the colour of the annulus when they matched in colour and slowing it when they differed. We show that the location of attention modulated the size of this priming effect. However, the primes were rendered invisible by metacontrast-masking and remained unseen despite being attended. Visual attention could therefore facilitate processing of an invisible target and cannot, therefore, be a sufficient precondition for visual awareness.
Notes:
Tanja C W Nijboer, Ryota Kanai, Edward H F de Haan, Maarten J van der Smagt (2008)  Recognising the forest, but not the trees: an effect of colour on scene perception and recognition.   Conscious Cogn 17: 3. 741-752 Sep  
Abstract: Colour has been shown to facilitate the recognition of scene images, but only when these images contain natural scenes, for which colour is 'diagnostic'. Here we investigate whether colour can also facilitate memory for scene images, and whether this would hold for natural scenes in particular. In the first experiment participants first studied a set of colour and greyscale natural and man-made scene images. Next, the same images were presented, randomly mixed with a different set. Participants were asked to indicate whether they had seen the images during the study phase. Surprisingly, performance was better for greyscale than for coloured images, and this difference is due to the higher false alarm rate for both natural and man-made coloured scenes. We hypothesized that this increase in false alarm rate was due to a shift from scrutinizing details of the image to recognition of the gist of the (coloured) image. A second experiment, utilizing images without a nameable gist, confirmed this hypothesis as participants now performed equally on greyscale and coloured images. In the final experiment we specifically targeted the more detail-based perception and recognition for greyscale images versus the more gist-based perception and recognition for coloured images with a change detection paradigm. The results show that changes to images are detected faster when image-pairs were presented in greyscale than in colour. This counterintuitive result held for both natural and man-made scenes (but not for scenes without nameable gist) and thus corroborates the shift from more detailed processing of images in greyscale to more gist-based processing of coloured images.
Notes:
Tanja C W Nijboer, Rob D McIntosh, Gudrun M S Nys, H Chris Dijkerman, A David Milner (2008)  Prism adaptation improves voluntary but not automatic orienting in neglect.   Neuroreport 19: 3. 293-298 Feb  
Abstract: Prism adaptation has been shown to temporarily ameliorate the symptoms of unilateral neglect. The underlying mechanisms of change are not yet fully understood. In this study, we investigate the influence of this treatment on attentional orienting under conditions of exogenous (peripheral onset) and endogenous (central symbolic) cueing. In one patient with left visual extinction and recovered neglect, and another patient with left visual neglect, visuo-motor adaptation to a rightward prismatic shift of 10 degrees improved leftward orienting of attention following an endogenous but not an exogenous cue; leftward re-orienting of attention was also improved in the endogenous task for the second patient. We suggest that prism adaptation may ameliorate neglect by improving compensatory processes of leftward voluntary orienting, rather than by a fundamental change in attentional bias.
Notes:
Tanja C W Nijboer, Carla Ruis, H Bart van der Worp, Edward H F De Haan (2008)  The role of Funktionswandel in metamorphopsia.   J Neuropsychol 2: Pt 1. 287-300 Mar  
Abstract: Patients with metamorphopsia perceive objects or faces as being distorted and/or different in size. In most cases, recognition is not impaired. The stimulus specificity, particularly in the case of face perception, has led to the suggestion that metamorphopsia is a deficit at the entry level of category-specific recognition systems; in this case, the face processing system. An explanation in terms of a visuosensory deficit (i.e., Funktionswandel) that affects the perception of specific stimulus categories has not been systematically evaluated. In this study, we report two patients (MZ and CM) who experienced hemi-metamorphopsia for faces after a stroke in the posterior part of the brain. Despite the distortions, they could still match and recognize faces. We carried out a detailed evaluation of their visual-sensory status and found that both MZ and CM had specific problems with discriminating and estimating sizes and shapes, especially in the contralesional visual field. It was concluded that these cases, metamorphopsia was not due to a higher-order perception impairment specific for faces, but rather of a specific impairment in shape perception in the contralesional visual field that proportionally affects the perception of faces.
Notes:
2007
Tanja C W Nijboer, Martine J E van Zandvoort, Edward H F de Haan (2007)  A familial factor in the development of colour agnosia.   Neuropsychologia 45: 8. 1961-1965 Apr  
Abstract: An important aspect of research into the link between genes and behaviour concerns the identification of familial determination. There is evidence for familial factors in selective deficits, such as developmental dyslexia and developmental prosopagnosia. Colour agnosia concerns a selective neuropsychological condition in which colour perception is intact, while the identification and naming of colour is disrupted. We recently demonstrated that this deficit can occur as a developmental deficit. Here, we show that there is a familial factor in the development of colour agnosia by reporting the colour processing abilities of the mother and the daughters of a man with developmental colour agnosia.
Notes:
Tanja C W Nijboer, Maarten J Van Der Smagt, Martine J E Van Zandvoort, Edward H F De Haan (2007)  Colour agnosia impairs the recognition of natural but not of non-natural scenes.   Cogn Neuropsychol 24: 2. 152-161 Mar  
Abstract: Scene recognition can be enhanced by appropriate colour information, yet the level of visual processing at which colour exerts its effects is still unclear. It has been suggested that colour supports low-level sensory processing, while others have claimed that colour information aids semantic categorization and recognition of objects and scenes. We investigated the effect of colour on scene recognition in a case of colour agnosia, M.A.H. In a scene identification task, participants had to name images of natural or non-natural scenes in six different formats. Irrespective of scene format, M.A.H. was much slower on the natural than on the non-natural scenes. As expected, neither M.A.H. nor control participants showed any difference in performance for the non-natural scenes. However, for the natural scenes, appropriate colour facilitated scene recognition in control participants (i.e., shorter reaction times), whereas M.A.H.'s performance did not differ across formats. Our data thus support the hypothesis that the effect of colour occurs at the level of learned associations.
Notes:
Martine J E van Zandvoort, Tanja C W Nijboer, Edward de Haan (2007)  Developmental colour agnosia.   Cortex 43: 6. 750-757 Aug  
Abstract: Colour agnosia concerns the inability to recognise colours despite intact colour perception, semantic memory for colour information, and colour naming. Patients with selective colour agnosia have been described and the deficit is associated with left hemisphere damage. Here we report a case study of a 43-year-old man who was referred to us with a stroke in his right cerebellar hemisphere. During the standard assessment it transpired that he was unable to name coloured patches. Detailed assessment of his colour processing showed that he suffers from a selective colour agnosia. As he claimed to have had this problem all his life, and the fact that the infratentorial infarct that he had incurred was in an area far away from the brain structures that are known to be involved in colour processing, we suggest that he is the first reported case of developmental colour agnosia.
Notes:
2006
Tanja C W Nijboer, Martine J E van Zandvoort, Edward H F de Haan (2006)  Seeing red primes tomato: evidence for comparable priming from colour and colour name primes to semantically related word targets.   Cogn Process 7: 4. 269-274 Dec  
Abstract: There is ample evidence that an independent processing stream exists that subserves the perception and appreciation of colour. Neurophysiological research has identified separate brain mechanisms for the processing of wavelength and colour, and neuropsychological studies have revealed selective colour disorders, such as achromatopsia, colour agnosia, and colour anomia. The aim of the present study is to investigate whether the perception of colour may, despite its independent processing, influence other cognitive functions. Specifically, we investigate the possibility that the perception of a colour influences higher order processes such as the activation of semantically related concepts. We designed an associative priming task involving a colour prime (e.g. a red patch or the word RED) and a lexical decision response to a semantically related ('tomato' vs. 'timato') or unrelated ('grass' vs. 'griss') word target. The results of this experiment indicate that there is comparable facilitation of accessing colour-related semantics through the perception of a colour or the reading of a colour name. This suggests that colour has a direct effect on higher order level, cognitive processing. These results are discussed in terms of current models of colour processing.
Notes:
Tanja C W Nijboer, Martine J E van Zandvoort, Edward H F de Haan (2006)  Covert colour processing in colour agnosia.   Neuropsychologia 44: 8. 1437-1443 01  
Abstract: Patients with colour agnosia can perceive colours and are able to match coloured patches on hue, but are unable to identify or categorise colours. It is a rare condition and there is as yet no agreement on the clinical definition or a generally accepted explanation. In line with observations from object agnosia and prosopagnosia, we hypothesised that (some of) these patients might still be able to process colour information at an implicit level. In this study, we investigated this possibility of implicit access to colour semantics and colour names in a man (MAH) who suffers from developmental colour agnosia. We designed two experimental computer tasks: an associative colour priming task with a lexical decision response and a reversed Stroop task. The results of these experiments suggest that there is indeed automatic processing of colour, although MAH was unable to explicitly use colour information.
Notes:
Powered by PublicationsList.org.