Motion contrast: a new metric for direction discrimination

被引:37
作者
Georgeson, MA [1 ]
Scott-Samuel, NE [1 ]
机构
[1] Univ Birmingham, Sch Psychol, Birmingham B15 2TT, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
motion; motion energy; motion detection; human vision; gratings; contrast; direction discrimination; flicker; contrast gain control;
D O I
10.1016/S0042-6989(99)00147-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The Adelson-Bergen energy model (Adelson, E. H., & Bergen, J. R. (1985). Spatiotemporal energy models for the perception of motion. Journal of the Optical Society of America A, 2, 284-299) is a standard framework for understanding first-order motion processing. The opponent energy for a given input is calculated by subtracting one directional energy measure (E-L) from its opposite (E-R), and its sign indicates the direction of motion of the input. Our observers viewed a dynamic sequence of gratings (1 c/deg) equivalent to the sum of two gratings moving in opposite directions with different contrasts. The ratio of contrasts was Varied across trials. We found that opponent energy was a very poor predictor of direction discrimination performance. Heeger (1992). Normalization of cell responses in cat striate cortex. Visual Neuroscience, 9, 181-197) has suggested that divisive inhibition amongst striate cells requires a contrast gain control in the energy model. A new metric can be formulated in the spirit of Heeger's model by normalising the opponent energy (E-L - E-R) with flicker energy, the sum of the directional motion energies (E-L + E-R). This new measure, motion contrast (E-L - E-R)/(E-L + E-R), was found to be a good predictor of direction discrimination performance over a wide range of contrast levels, but opponent energy was not. Discrimination thresholds expressed as motion contrast were around 0.5 +/- 0.1 for the sampled drifting gratings used in our experiments. We show that the dependence on motion contrast, and the threshold of about 0.5, can be predicted by a modified opponent energy model based on current knowledge of the response functions and response variance of cortical cells. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4393 / 4402
页数:10
相关论文
共 30 条
[1]   SPATIOTEMPORAL ENERGY MODELS FOR THE PERCEPTION OF MOTION [J].
ADELSON, EH ;
BERGEN, JR .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1985, 2 (02) :284-299
[2]  
ADELSON EH, 1986, P IEEE WORKSH MOT RE
[3]   MOTION SELECTIVITY AND THE CONTRAST-RESPONSE FUNCTION OF SIMPLE CELLS IN THE VISUAL-CORTEX [J].
ALBRECHT, DG ;
GEISLER, WS .
VISUAL NEUROSCIENCE, 1991, 7 (06) :531-546
[4]  
[Anonymous], 1996, VISUAL PERCEPTION
[5]  
BRITTEN KH, 1992, J NEUROSCI, V12, P4745
[6]   DIRECTIONALLY SELECTIVE COMPLEX CELLS AND THE COMPUTATION OF MOTION ENERGY IN CAT VISUAL-CORTEX [J].
EMERSON, RC ;
BERGEN, JR ;
ADELSON, EH .
VISION RESEARCH, 1992, 32 (02) :203-218
[7]   HUMAN LUMINANCE PATTERN-VISION MECHANISMS - MASKING EXPERIMENTS REQUIRE A NEW MODEL [J].
FOLEY, JM .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION, 1994, 11 (06) :1710-1719
[8]   Visual cortex neurons in monkeys and cats: Detection, discrimination, and identification [J].
Geisler, WS ;
Albrecht, DG .
VISUAL NEUROSCIENCE, 1997, 14 (05) :897-919
[9]  
GREEN DM, 1974, SIGNAL DETECTION THE
[10]   NORMALIZATION OF CELL RESPONSES IN CAT STRIATE CORTEX [J].
HEEGER, DJ .
VISUAL NEUROSCIENCE, 1992, 9 (02) :181-197