ライフサイエンスコーパス: afterimage

1 filled-in surface during adaptation (global afterimage).

2 concentration-specific information--an odor afterimage.

3 , these signals might contribute to negative afterimages.

4 ject was aware both of the stimuli and their afterimages.

5 aptation than with the strength of the local afterimages.

6 edicts well the observed properties of color afterimages.

7 ction between binocular rivalry and negative afterimages (AIs).

8 Afterimages also prove invaluable in exploring selective

9 d the response to stimuli that produce color afterimages and found that these stimuli, like real colo

10 Thus, global afterimages are not merely by-products of local afterima

11 that the perceptual phenomena of fading and afterimages are shaped by both cortical and subcortical

12 rimages corresponding to the inducers (local afterimages), but also to one corresponding to the perce

13 erimages are not merely by-products of local afterimages, but involve adaptation at a cortical repres

14 The strength of the global afterimage correlated to a greater extent with perceptua

15 ading configuration led not only to negative afterimages corresponding to the inducers (local afterim

16 phenomenon revealing that the perception of afterimages depends not only on bodily signals, but also

17 These data show that afterimage drifts in the Taylor illusion do not only dep

18 The effect of ownership on afterimage drifts is associated with beta/gamma power an

19 consciously seeing the grating increases the afterimage duration.

20 humans (both males and females) by measuring afterimage durations over the entire range of inducer st

21 n >33% of patients: palinopsia (trailing and afterimages), entoptic phenomena (floaters, blue field e

22 ct of visual perception that causes negative afterimages, fading, and many other visual illusions.

23 ety of striking percepts, including negative afterimages, fading, and motion aftereffects.

24 We investigated the duration of afterimages for all four combinations of high versus low

25 Afterimage formation, historically attributed to retinal

26 Nevertheless, red afterimages, generated by chromatic modulation toward th

27 responses can reveal the processing of color afterimages in the absence of primary visual cortex and

28 An afterimage induced by prior adaptation to a visual stimu

29 daptor was suppressed, the more strongly the afterimage intensity was reduced.

30 Our results imply that formation of afterimages involves neuronal structures that access inp

31 to the odor presentation, implying that the afterimage is not primarily peripheral.

32 erimage of the wheel, yet by definition this afterimage is stationary on the retina.

33 e presented for cortical generation of color afterimages is explainable by spatiotemporal factors tha

34 ol we show that the strength of the negative afterimage of an adaptor was reduced by half when it was

35 on: the flicker can also be perceived on the afterimage of the wheel, yet by definition this afterima

36 subject (D.B.), who reports conscious visual afterimages of stimuli of which he is unaware when they

37 In the Taylor illusion, the size of an afterimage projected on one's hand changes according to

38 body: in the Taylor illusion, the size of an afterimage projected on one's hand changes according to

39 We found that an afterimage projected on the participant's hand drifted d

40 We found that visual afterimages projected on the participant's hand drifted

41 Proposed physiological mechanisms for color afterimages range from bleaching of cone photopigments t

42 Our results indicate that afterimage signals are generated in the retina but may b

43 generate rebound responses that can provide afterimage signals for later neurons.

44 nd that there is a centrally maintained odor afterimage, similar to other sensory systems.

45 We report a type of afterimage that appears to require cortical adaptation.

46 In the Taylor illusion, the perceived afterimage that is projected on an observer's hand will

47 The strength and persistence of the afterimage was dependent on the duration of both artific

48 The odor afterimage was not dependent on odorant physicochemical

49 By using afterimages, we provide strong evidence that the human v

50 Afterimages were important in disproving the theory that

51 These afterimages were mutually exclusive, undergoing monocula

52 to the grating decreases the duration of its afterimage, whereas consciously seeing the grating incre

53 introduce a time-varying method for evoking afterimages, which provides precise measurements of adap