Retinal Encoding of Ultrabrief Shape Recognition Cues
被引:13
作者:
Greene, Ernest
论文数: 0引用数: 0
h-index: 0
机构:
Univ So Calif, Dept Psychol, Lab Neurometr Res, Los Angeles, CA 90089 USA
Neuropsychol Fdn, Sun Valley, CA USAUniv So Calif, Dept Psychol, Lab Neurometr Res, Los Angeles, CA 90089 USA
Greene, Ernest
[1
,2
]
机构:
[1] Univ So Calif, Dept Psychol, Lab Neurometr Res, Los Angeles, CA 90089 USA
[2] Neuropsychol Fdn, Sun Valley, CA USA
来源:
PLOS ONE
|
2007年
/
2卷
/
09期
关键词:
D O I:
10.1371/journal.pone.0000871
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Shape encoding mechanisms can be probed by the sequential brief display of dots that mark the boundary of the shape, and delays of less that a millisecond between successive dots can impair recognition. It is not entirely clear whether this is accomplished by preserving stimulus timing in the signal being sent to the brain, or calls for a retinal binding mechanism. Two experiments manipulated the degree of simultaneity among and within dot pairs, requiring also that the pair members be in the same half of the visual field or on opposite halves, i.e., across the midline from one another. Recognition performance was impaired the same for these two conditions. The results make it likely that simultaneity of cues is being registered within the retina. A potential mechanism is suggested, calling for linkage of stimulated sites through activation of PA1 cells. A third experiment confirmed a prior finding that the overall level of recognition deficit is partly a function of display-set size, and affirmed submillisecond resolution in binding dot pairs into effective shape-recognition cues.