Blasdel G G
Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115.
J Neurosci. 1992 Aug;12(8):3139-61. doi: 10.1523/JNEUROSCI.12-08-03139.1992.
Maps of orientation preference and selectivity, inferred from differential images of orientation (Blasdel, 1992), reveal linear organizations in patches, 0.5-1.0 mm across, where orientation selectivities are high, and where preferred orientations rotate linearly along one axis while remaining constant along the other. Most of these linear zones lie between the centers of adjacent ocular dominance columns, with their short iso-orientation slabs oriented perpendicular, in regions enjoying the greatest binocular overlap. These two-dimensional linear zones are segregated by one- and zero-dimensional discontinuities that are particularly abundant in the centers of ocular dominance columns, and that are also correlated with cytochrome oxidase-rich zones within them. Discontinuities smaller than 90 degrees extend in one dimension, as fractures, while discontinuities greater than 90 degrees are confined to points, in the form of singularities, that are generated when orientation preferences rotate continuously through +/- 180 degrees along circular paths. The continuous rotations through 180 degrees imply that direction preferences are not organized laterally in striate cortex. And they also ensure that preferences for all orientations converge at each singularity, with perpendicular orientations represented uniquely close together on opposite sides. The periodic interspersing of linear zones and singularities suggests that orientation preferences are organized by at least two competing schemes. They are optimized for linearity, along with selectivity and binocularity, in the linear zones, and they are optimized for density near singularities. Since upper-layer neurons are likely to have similarly sized dendritic fields in all regions (Lund and Yoshioka, 1991), those in the linear zones should receive precise information about narrowly constrained orientations, while those near singularities should receive coarse information about all orientations--very different inputs that suggest different perceptual functions.
从方向差异图像推断出的方向偏好和选择性图谱(Blasdel,1992)显示,在直径为0.5 - 1.0毫米的斑块中存在线性组织,这些斑块中方向选择性较高,且偏好方向沿一个轴线性旋转,而沿另一个轴保持不变。这些线性区域大多位于相邻眼优势柱的中心之间,其短的等方向平板垂直排列,处于双眼重叠最大的区域。这些二维线性区域被一维和零维的不连续区域分隔开,这些不连续区域在眼优势柱的中心特别丰富,并且也与其中富含细胞色素氧化酶的区域相关。小于90度的不连续区域在一个维度上延伸,呈裂缝状,而大于90度的不连续区域局限于点,呈奇点形式,当方向偏好沿圆形路径连续旋转±180度时产生。180度的连续旋转意味着方向偏好在纹状皮层中不是横向组织的。而且它们还确保所有方向的偏好在每个奇点处汇聚,垂直方向在相对两侧独特地紧密排列。线性区域和奇点的周期性交错表明方向偏好是由至少两种相互竞争的方案组织的。它们在线性区域中针对线性以及选择性和双眼性进行了优化,而在奇点附近针对密度进行了优化。由于上层神经元在所有区域可能具有大小相似的树突场(Lund和Yoshioka,1991),因此线性区域中的神经元应该接收关于狭窄受限方向的精确信息,而奇点附近的神经元应该接收关于所有方向的粗略信息——这是非常不同的输入,暗示了不同的感知功能。