Visual object processing in the inferotemporal cortex

描述（由申请人提供）：视觉物体识别是我们行为的核心，了解潜在的大脑机制对于理解人类视觉感知和记忆至关重要。关键问题是创建对象身份的选择性，该对象身份允许对象视网膜图像的变化，例如位置和大小的变化。灵长类动物的大脑似乎在腹侧视觉流中构建了这种选择性，因为该视觉流的最高区域-前颞下皮层（AIT）-的神经元反应显示出形状选择性，可以容忍位置和大小的变化。然而，我们并不了解这些关键的神经元特性-AIT耐受性的报告是有限的和不一致的，最近的研究表明，它可以非常有限。因此，本提案的目标是了解可能决定AIT位置和尺寸公差的关键因素，并确定AIT公差是否可以解释行为公差。 我们的第一个目标是系统地确定AIT神经元形状选择性的位置和大小公差的范围内的对象集和对象训练的历史。我们将建立选择性与AIT位置和尺寸公差的关系，AIT位置和尺寸公差的相互作用，以及针对特定对象的训练对这些关系的影响。这些数据将在灵长类动物视觉系统的最高水平建立神经元耐受性，并为进一步研究提供急需的基础。 可能构成位置和尺寸公差基础的机制分为两大类：（1）自动泛化;（2）通过体验对象的位置和尺寸变化来学习公差。我们的第二个目标是确定位置或大小特定的对象的经验有实质性的影响的位置或大小公差的AIT形状的选择性。由于尚未对此进行研究，任何结果都将在约束机制和指导未来研究方面提供极其丰富的信息。 虽然人们认为AIT耐受性是行为耐受性的基础，但这还没有得到系统的研究。我们的第三个目标是确定是否可以解释的AIT神经元形状选择性的公差的位置和大小公差的对象识别。这对于理解高水平腹侧流神经元反应和视觉物体识别之间的联系至关重要。

DESCRIPTION (provided by applicant): Visual object recognition is central to our behavior, and knowledge of the underlying brain mechanisms is critical to understanding human visual perception and memory. The key problem is creation of selectivity for object identity that tolerates changes in an object's retinal image, such as changes in position and size. The primate brain appears to construct this selectivity in the ventral visual stream because neuronal responses in the highest area of that stream--the anterior inferotemporal cortex (AIT)--show shape selectivity that can tolerate position and size changes. Yet, we do not understand these key neuronal properties--reports of AIT tolerance are limited and inconsistent, and recent studies show that it can be very restricted. Thus, the goals of this proposal are an understanding of key factors likely to determine AIT position and size tolerance, and to determine if AIT tolerance can explain behavioral tolerance. Our first aim is to systematically determine the position and size tolerance of AIT neuronal shape selectivity for a range of object sets and object training histories. We will establish the relationship of selectivity and AIT position and size tolerance, the interaction of AIT position and size tolerance, and the effect of object-specific training on these relationships. These data will establish neuronal tolerance at the highest level of the primate visual system and provide a much-needed foundation for further study. The mechanisms that might underlie position and size tolerance fall into two broad classes: (1) automatic generalization; and (2) tolerance learned by experiencing objects across changes in position and size. Our second aim is to determine if position- or size-specific object experience have substantial effects on the position or size tolerance of AIT shape selectivity. Because this has not been examined, any result would be extremely informative in constraining mechanisms and guiding future studies. Although it is thought that AIT tolerance underlies behavioral tolerance, this has not been systematically examined. Our third aim is to determine if the position and size tolerance of object identification can be explained by the tolerance of AIT neuronal shape selectivity. This is a vital to understanding the link between high-level, ventral stream neuronal responses and visual object identification.