Larsson J, Amunts K, Gulyás B, Malikovic A, Zilles K, Roland P E
Division of Human Brain Research, Department of Neuroscience, Karolinska Institute, S-171 77 Stockholm, Sweden.
Eur J Neurosci. 1999 Nov;11(11):4024-36. doi: 10.1046/j.1460-9568.1999.00805.x.
Illusory contours provide a striking example of the visual system's ability to extract a meaningful representation of the surroundings from fragmented visual stimuli. Psychophysical and neurophysiological data suggest that illusory contours are processed in early visual cortical areas, and neuroimaging studies in humans have shown that Kanizsa-type illusory contours activate early retinotopic visual areas that are also activated by real contours. It is not known whether other types of illusory contours are processed by the same mechanisms, nor is it clear to what extent attentional effects may have influenced these results, as no attempt was made to match the salience of real and illusory stimuli in previous imaging studies. It therefore remains an open question whether there are any brain regions specifically involved in the perception of illusory contours. To address these questions, we have used 15O-butanol positron emission tomography (PET) and a novel kind of illusory contour stimulus that is induced only by aligned line ends. By employing a form discrimination task that was matched for attention and stimulus salience across conditions we were able to directly contrast perception of real and illusory contours. We found that the regions activated by illusory contour perception were the same as those activated by real contours. Only one region, located in the right fusiform gyrus, was significantly more strongly activated by perception of illusory contours than by real contours. In addition, a principal component analysis suggested that illusory contour perception is associated with a change in the correlation between V1 and V2. We conclude that different kinds of illusory contours are processed by the same cortical regions and that these regions overlap extensively with those involved in processing of real contours. At the regional level, perception of illusory contours thus appears to differ from perception of real contours by the degree of involvement of higher visual areas as well as by the nature of interaction between early visual areas.
错觉轮廓提供了一个引人注目的例子,说明视觉系统能够从碎片化的视觉刺激中提取有意义的周围环境表征。心理物理学和神经生理学数据表明,错觉轮廓在早期视觉皮层区域进行处理,而对人类的神经成像研究表明,卡尼萨型错觉轮廓会激活早期视网膜拓扑视觉区域,这些区域也会被真实轮廓激活。目前尚不清楚其他类型的错觉轮廓是否通过相同的机制进行处理,也不清楚注意力效应在多大程度上可能影响了这些结果,因为在之前的成像研究中没有尝试匹配真实和错觉刺激的显著性。因此,是否存在专门参与错觉轮廓感知的脑区仍然是一个悬而未决的问题。为了解决这些问题,我们使用了15O-丁醇正电子发射断层扫描(PET)和一种新型的错觉轮廓刺激,这种刺激仅由对齐的线段末端诱导产生。通过采用一种在不同条件下匹配注意力和刺激显著性的形状辨别任务,我们能够直接对比真实轮廓和错觉轮廓的感知。我们发现,错觉轮廓感知激活的区域与真实轮廓激活的区域相同。只有一个位于右侧梭状回的区域,错觉轮廓感知比真实轮廓感知激活得明显更强。此外,主成分分析表明,错觉轮廓感知与V1和V2之间的相关性变化有关。我们得出结论,不同类型的错觉轮廓由相同的皮层区域处理,并且这些区域与参与真实轮廓处理的区域广泛重叠。在区域层面上,错觉轮廓的感知因此似乎与真实轮廓的感知不同,体现在更高视觉区域的参与程度以及早期视觉区域之间相互作用的性质上。