Stockman A, MacLeod D I, DePriest D D
Department of Psychology, University of California at San Diego, La Jolla 92093.
Vision Res. 1991;31(2):189-208. doi: 10.1016/0042-6989(91)90111-h.
Flicker modulation sensitivity measurements made on high intensity orange steady backgrounds indicate that signals from short-wavelength sensitive cones (S-cones) have access to two pathways. At low S-cone adaptation levels the frequency response falls quickly with increasing frequency, but at higher adaptation levels it extends to much higher frequencies. At these higher S-cone adaptation levels, the following procedures can selectively expose either a process sensitive to low frequencies or one more sensitive to higher frequencies: (1) at high flicker frequencies, the S-cone signal can be nulled by a long-wavelength sensitive cone (L-cone) signal of suitable amplitude and phase, but at low frequencies a residual flicker persists; the modulation sensitivity for the residual flicker is lowpass in shape with a rapid decline in sensitivity with increasing flicker frequency; (2) sensitivity to flicker in the presence of a 17 Hz S- or L-cone mask is also lowpass with a similarly steep loss of high frequency sensitivity; yet (3) sensitivity to flicker during transient stimulation of the S-cones at 0.5 Hz is comparatively wideband (and slightly bandpass) in shape. The S-cone signal produced by the high frequency process is almost as well-maintained towards high frequencies as M- and L-cone signals. Furthermore, it is capable of participating in flicker photometric nulls with M- and L-cone signals. At low frequencies, however, when the low frequency S-cone signal is also present, satisfactory nulls can not be found. From these and phenomenological considerations, we identify the low and high frequency S-cone processes as S-cone inputs to the chromatic and luminance pathways, respectively. The phase adjustments needed to optimize flicker photometric nulls reveal that the S-cone input to the luminance pathway is actually inverted, but this is demonstrable only at relatively low frequencies: at medium or high frequencies the S-cone influence can be synergistic with that of the other cone types because of a delay in the transmission of S-cone signals.
在高强度橙色稳定背景下进行的闪烁调制灵敏度测量表明,来自短波敏感视锥细胞(S-视锥细胞)的信号有两条通路。在低S-视锥细胞适应水平时,频率响应随频率增加而迅速下降,但在较高适应水平时,其延伸到更高频率。在这些较高的S-视锥细胞适应水平下,以下程序可以选择性地揭示对低频敏感的过程或对高频更敏感的过程:(1)在高闪烁频率下,S-视锥细胞信号可以被具有合适幅度和相位的长波敏感视锥细胞(L-视锥细胞)信号抵消,但在低频时仍有残留闪烁;残留闪烁的调制灵敏度呈低通形状,随着闪烁频率增加灵敏度迅速下降;(2)在存在17Hz S-或L-视锥细胞掩蔽时对闪烁的灵敏度也是低通的,高频灵敏度有类似的急剧损失;然而(3)在0.5Hz对S-视锥细胞进行瞬态刺激期间对闪烁的灵敏度形状相对宽带(且略呈带通)。高频过程产生的S-视锥细胞信号在高频时几乎与M-和L-视锥细胞信号一样能良好保持。此外,它能够与M-和L-视锥细胞信号一起参与闪烁光度抵消。然而,在低频时,当低频S-视锥细胞信号也存在时,无法找到令人满意的抵消。基于这些以及现象学上的考虑,我们将低频和高频S-视锥细胞过程分别识别为S-视锥细胞对色度和亮度通路的输入。优化闪烁光度抵消所需的相位调整表明,S-视锥细胞对亮度通路的输入实际上是反转的,但这仅在相对低频时可证明:在中高频时,由于S-视锥细胞信号传输延迟,S-视锥细胞的影响可能与其他视锥细胞类型的影响协同。