Horridge Adrian
Biological Sciences, Australian National University, Canberra, ACT, Australia.
Eye Brain. 2015 Oct 5;7:83-107. doi: 10.2147/EB.S89201. eCollection 2015.
In the 1920s, Mathilde Hertz found that trained bees discriminated between shapes or patterns of similar size by something related to total length of contrasting contours. This input is now interpreted as modulation in green and blue receptor channels as flying bees scan in the horizontal plane. Modulation is defined as total contrast irrespective of sign multiplied by length of edge displaying that contrast, projected to vertical, therefore, combining structure and contrast in a single input. Contrast is outside the eye; modulation is a phasic response in receptor pathways inside. In recent experiments, bees trained to distinguish color detected, located, and measured three independent inputs and the angles between them. They are the tonic response of the blue receptor pathway and modulation of small-field green or (less preferred) blue receptor pathways. Green and blue channels interacted intimately at a peripheral level. This study explores in more detail how various patterns are discriminated by these cues. The direction of contrast at a boundary was not detected. Instead, bees located and measured total modulation generated by horizontal scanning of contrasts, irrespective of pattern. They also located the positions of isolated vertical edges relative to other landmarks and distinguished the angular widths between vertical edges by green or blue modulation alone. The preferred inputs were the strongest green modulation signal and angular width between outside edges, irrespective of color. In the absence of green modulation, the remaining cue was a measure and location of blue modulation at edges. In the presence of green modulation, blue modulation was inhibited. Black/white patterns were distinguished by the same inputs in blue and green receptor channels. Left-right polarity and mirror images could be discriminated by retinotopic green modulation alone. Colors in areas bounded by strong green contrast were distinguished as more or less blue than the background. The blue content could also be summed over the whole target. There were no achromatic patterns for bees and no evidence that they detected black, white, or gray levels apart from the differences in blue content or modulation at edges. Most of these cues would be sensitive to background color but some were influenced by changes in illumination. The bees usually learned only to avoid the unrewarded target. Exactly the same preferences of the same inputs were used in the detection of single targets as in discrimination between two targets.
20世纪20年代,玛蒂尔德·赫兹发现,经过训练的蜜蜂能够通过与对比轮廓总长度相关的因素来区分大小相似的形状或图案。当飞行的蜜蜂在水平面上扫描时,这种输入现在被解释为绿色和蓝色受体通道中的调制。调制被定义为不考虑符号的总对比度乘以显示该对比度的边缘长度,并投影到垂直方向,因此,在单个输入中结合了结构和对比度。对比度在眼睛之外;调制是内部受体通路中的一种相位响应。在最近的实验中,经过训练以区分颜色的蜜蜂检测、定位并测量了三个独立的输入以及它们之间的角度。它们是蓝色受体通路的紧张性反应以及小视野绿色或(较不偏好的)蓝色受体通路的调制。绿色和蓝色通道在周边水平密切相互作用。本研究更详细地探讨了这些线索如何区分各种图案。边界处对比度的方向未被检测到。相反,蜜蜂定位并测量了由对比的水平扫描产生的总调制,而不考虑图案。它们还相对于其他地标定位了孤立垂直边缘的位置,并仅通过绿色或蓝色调制区分垂直边缘之间的角宽度。首选输入是最强的绿色调制信号和外部边缘之间的角宽度,与颜色无关。在没有绿色调制的情况下,其余线索是边缘处蓝色调制的测量和位置。在存在绿色调制的情况下,蓝色调制受到抑制。黑白图案通过蓝色和绿色受体通道中的相同输入来区分。左右极性和镜像可以仅通过视网膜定位的绿色调制来区分。由强烈绿色对比界定的区域中的颜色与背景相比,被区分为或多或少的蓝色。蓝色含量也可以在整个目标上求和。对蜜蜂来说没有消色差图案,也没有证据表明它们除了边缘处蓝色含量或调制的差异外,还能检测到黑色、白色或灰色水平。这些线索中的大多数对背景颜色敏感,但有些受到光照变化的影响。蜜蜂通常只学会避开无奖励的目标。在检测单个目标时,与区分两个目标时一样,使用相同输入的完全相同的偏好。