Maddess T
Proc R Soc Lond B Biol Sci. 1986 Sep 22;228(1253):433-59. doi: 10.1098/rspb.1986.0062.
A powerful effect resembling an afterimage is demonstrated on the pathway to the motion-sensitive neuron H1. This effect is independent of the locally generated gain control described in an earlier paper (Maddess & Laughlin 1985, Proc. R. Soc. Lond. B 225, 251). The afterimage, produced across the eye by a stationary pattern, causes the sensitivity to movement to be different according to the local stimulus history, and the effects of low-contrast (0.1) patterns, presented for as little as a few hundred milliseconds, remain for up to 2 s. Moving patterns interact with the afterimage to modulate the spike rate of H1. The afterimage increases with contrast but saturates at contrasts above 0.5. Low spatial frequencies generate afterimages less effectively than moderate ones; this result indicates that the afterimage process could lie at, or after, lateral inhibition between tonic units. This is supported by the fact that the altered sensitivity profiles generated by single bright and dark vertical bars initially resemble Mach bands. However, this character alters as the afterimage decays, and the depression of H1's response to moving bright stimuli, produced by the afterimage of a dark bar, continues to grow for up to 1 s after the adapting bar is removed. A short-lived (0.5 s) reduction of H1's directional selectivity accompanies strong afterimage formation. All these factors, especially the saturation at low contrasts and the spatial frequency tuning, rule out light adaptation by photoreceptors as the afterimage source. Luminances used were also low enough to exclude influence by the pupil mechanism. Lastly, responses to patterns that are occasionally jumped by large or small distances are broadened by stimuli that produce an afterimage. Responses to small displacements have previously been described as 'velocity impulse responses' (Srinivasan 1983, Vision Res. 23, 659; Zaagman et al. 1983, IEEE Trans. SMC 13, 900) and so the response broadening (stimulus blurring) can be taken as a reduction of the fly's temporal resolution of moving objects. Previously reported work shows that afterimages seen in humans and the effect reported here act over the same range of temporal frequencies rather than retinal drift speeds. This may suggest an important role for afterimage-like effects in the processing of the low temporal frequency components of moving images. Certainly, the fly's afterimage system reduces the visibility of moving objects within patches of an image that, have on average, contained slowly varying motion signals.(ABSTRACT TRUNCATED AT 400 WORDS)
在通向运动敏感神经元H1的通路上,展示出了一种类似于后像的强大效应。这种效应独立于早期一篇论文(Maddess和Laughlin,1985年,《伦敦皇家学会学报B》225卷,251页)中描述的局部产生的增益控制。由静止图案在整个眼睛上产生的后像,会使对运动的敏感度根据局部刺激历史而有所不同,并且低对比度(0.1)图案仅呈现几百毫秒,其效应会持续长达2秒。移动图案与后像相互作用,以调节H1的放电频率。后像随对比度增加,但在对比度高于0.5时会饱和。低空间频率产生后像的效果不如中等空间频率有效;这一结果表明后像过程可能位于强直单位之间的侧向抑制处或之后。单个明亮和黑暗垂直条产生的敏感度变化曲线最初类似于马赫带,这一事实支持了这一点。然而,随着后像衰减,这种特征会改变,并且由暗条的后像产生的H1对移动明亮刺激的反应抑制,在适应条移除后会持续增长长达1秒。强烈的后像形成伴随着H1方向选择性的短暂(0.5秒)降低。所有这些因素,尤其是低对比度下的饱和以及空间频率调谐,排除了光感受器的光适应作为后像来源的可能性。所使用的亮度也足够低,以排除瞳孔机制的影响。最后,对偶尔有大或小距离跳跃的图案的反应,会被产生后像的刺激拓宽。对小位移的反应先前被描述为“速度脉冲反应”(Srinivasan,1983年,《视觉研究》23卷,659页;Zaagman等人,1983年,《IEEE系统、人与控制论学报》13卷,900页),因此反应拓宽(刺激模糊)可被视为苍蝇对移动物体时间分辨率的降低。先前报道的工作表明,人类看到的后像和这里报道的效应在相同的时间频率范围内起作用,而不是视网膜漂移速度。这可能表明类似后像的效应在处理移动图像的低时间频率成分中起着重要作用。当然,苍蝇的后像系统降低了图像斑块内移动物体的可见性,这些斑块平均包含缓慢变化的运动信号。(摘要截取自400字)