Abstract

Simple SummaryDirectional preference neurons has been found in many vertebrate sensory systems. The isthmi pars magnocellularis (Imc) in avian midbrain, playing a key role in visual selective attention, shows impressive motion directional preference, but little is known about the physiological basis of this phenomenon. Herein, artificial visual stimuli, statistical analyses, and a neural computational model were used to unravel this mystery. This study deepens the understanding of the relationship between the directional preference and special receptive field structure of pigeon’s (Columba livia) Imc neuron.Neurons responding sensitively to motions in several rather than all directions have been identified in many sensory systems. Although this directional preference has been demonstrated by previous studies to exist in the isthmi pars magnocellularis (Imc) of pigeon (Columba livia), which plays a key role in the midbrain saliency computing network, the dynamic response characteristics and the physiological basis underlying this phenomenon are unclear. Herein, dots moving in 16 directions and a biologically plausible computational model were used. We found that pigeon Imc’s significant responses for objects moving in preferred directions benefit the long response duration and high instantaneous firing rate. Furthermore, the receptive field structures predicted by a computational model, which captures the actual directional tuning curves, agree with the real data collected from population Imc units. These results suggested that directional preference in Imc may be internally prebuilt by elongating the vertical axis of the receptive field, making predators attack from the dorsal-ventral direction and conspecifics flying away in the ventral-dorsal direction, more salient for avians, which is of great ecological and physiological significance for survival.

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