Extensive experimental studies have shown that in lower mammals, neuronal orientation preference in the primary visual cortex is organized in disordered "salt-and-pepper" organizations. In contrast, higher-order mammals display a continuous variation in orientation preference, forming pinwheel-like structures. Despite these observations, the spiking mechanisms underlying the emergence of these distinct topological structures and their functional roles in visual processing remain poorly understood. To address this, we developed a self-evolving spiking neural network model with Hebbian plasticity, trained using physiological parameters characteristic of rodents, cats, and primates, including retinotopy, neuronal morphology, and connectivity patterns. Our results identify critical factors, such as the degree of input visual field overlap, neuronal connection range, and the balance between localized connectivity and long-range competition, that determine the emergence of either salt-and-pepper or pinwheel-like topologies. Furthermore, we demonstrate that pinwheel structures exhibit lower wiring costs and enhanced sparse coding capabilities compared to salt-and-pepper organizations. They also maintain greater coding robustness against noise in naturalistic visual stimuli. These findings suggest that such topological structures confer significant computational advantages in visual processing and highlight their potential application in the design of brain-inspired deep learning networks and algorithms.

During natural evolution, the primary visual cortex (V1) of lower mammals typically forms salt-and-pepper organizations, while higher mammals and primates develop pinwheel structures with distinct topological properties. Despite the general belief that V1 neurons primarily serve as edge detectors, the functional advantages of pinwheel structures over salt-and-peppers are not well recognized. To this end, we propose a two-dimensional self-evolving spiking neural network that integrates Hebbian-like plasticity and empirical morphological data. Through extensive exposure to image data, our network evolves from salt-and-peppers to pinwheel structures, with neurons becoming localized bandpass filters responsive to various orientations. This transformation is accompanied by an increase in visual field overlap. Our findings indicate that neurons in pinwheel centers (PCs) respond more effectively to complex spatial textures in natural images, exhibiting quicker responses than those in salt-and-pepper organizations. PCs act as first-order stage processors with heightened sensitivity and reduced latency to intricate contours, while adjacent iso-orientation domains serve as second-order stage processors that refine edge representations for clearer perception. This study presents the first theoretical evidence that pinwheel structures function as crucial detectors of spatial contour saliency in the visual cortex.