Two auditory aftereffects and their dependency on carrier frequency

It is suggested that aftereffects caused by swept change of sound level (Reinhardt-Rutland & Anstis, Note 1) may contribute to auditory motion aftereffects (Grantham & Wightman, 1979). The latter appear to show selectivity for frequency; they are substantial if the frequency is .5 kHz but not if it is 2 kHz. An experiment was carried out to show to what extent there is such selectivity for aftereffects from swept sound-level change; this showed that they are substantial over a much wider range of frequencies than auditory motion aftereffects. It is concluded that the frequency selectivity of auditory motion aftereffects might be explained by frequency selectivity for inter-aural phase differences.     

Effects of situational cues on prism-induced aftereffects

A test was made of the hypothesis that external stimuli present during exposure to lateral displacement of the visual field can serve as situational cues whose presence or absence will influence the magnitude of aftereffects manifested subsequent to adaptation resulting from the exposure. The results indicated that the relative aftereffects were significantly greater when thenondisplacing goggles were worn during the periods in which aftereffect measurements were taken than was the case when they were removed during these test periods. The finding that manipulation of certain cues, i.e., the restriction of the visual field, weight, etc., of the goggles, associated with the adaptation period can in part determine the size of observed aftereffects provides evidence in support of the notion that aftereffects can be conditioned to precisely given constellations of stimuli In addition, the need for caution in conceptualizing aftereffects as simply the persistence of adaptive shifts once visual displacement has been terminated is suggested.     

Buildup and decay of a three-dimensional rotational aftereffect obtained with a three-dimensional figure

Gaps in past literature have raised questions regarding the kinds of stimuli that can lead to three-dimensional (3-D) rotation aftereffects. Further, the characteristics of the buildup and decay of such aftereffects are not clear. In the present experiments, rotation aftereffects were generated by projections of cube-like stimuli whose dynamic perspective motions gave rise to the perception of rotation in unambiguous directions; test stimuli consisted of similar cubes whose rotation directions were ambiguous. In experiment 1, the duration of the adaptation stimulus was varied and it was found that the 3-D rotation aftereffect develops with a time constant of approximately 26 s. In experiment 2, the duration between adaptation and testing was varied. It was found that the 3-D rotation aftereffect has a decay constant of about 9 s, similar to that observed with 2-D motion aftereffects. Experiment 3 showed that the rotation aftereffects were not simple depth aftereffects. To account for these aftereffects and related data, a modification of an existing neural-network model is suggested.     

Aftereffects for face attributes with different natural variability: Children are more adaptable than adolescents

Adults can be adapted to a particular facial distortion in which both eyes are shifted symmetrically (Robbins, R., McKone, E., & Edwards, M. (2007). Aftereffects for face attributes with different natural variability: Adapter position effects and neural models. Journal of Experimental Psychology: Human Perception and Performance, 33, 570–592), but they do not show as great adaptation to an asymmetrical eye distortion. We adapted children and adolescents to symmetrical and asymmetrical eye distortions and measured the aftereffects. Children (aged 6–12, mean age 9 years) showed larger aftereffects than adolescents (aged 13–18, mean age 15 years) and demonstrated aftereffects of a similar magnitude for both asymmetrical and symmetrical distortions. Adolescents only showed aftereffects for symmetrical distortions. We propose that children may have a more flexible face norm and neural responses that allow a broader range of adapted states compared to adolescents.     

Adaptation to biological motion leads to a motion and a form aftereffect

Recent models have proposed a two-stage process of biological motion recognition. First, template or snapshot neurons estimate the body form. Then, motion is estimated from body form change. This predicts separate aftereffects for body form and body motion. We tested this prediction. Observers viewing leftward- or rightward-facing point-light walkers that walked forward or backward subsequently experienced oppositely directed aftereffects in stimuli ambiguous in the facing or the walking direction. These aftereffects did not originate from adaptation to the motion of the individual light points, because they occurred for limited-lifetime stimuli that restrict local motion. They also occurred when the adaptor displayed a random sequence of body postures that did not induce the walking motion percept. We thus conclude that biological motion gives rise to separate form and motion aftereffects and that body form representations are involved in biological motion perception.     

Motion integration during motion aftereffects

The perceived global motion of a stimulus depends on how its different local motion-direction vectors are distributed in space and time. When they are explicitly co-localized, as in the case of locally paired motion, competitive motion integration mechanisms produce a unitary global motion direction determined by their vector average. During motion aftereffects induced by simultaneous adaptation to multiple motion directions, just as in the case of locally paired motion, different directional signals originate simultaneously from exactly the same position in space. Therefore, the perceived global motion direction during motion aftereffects results from local vector averaging of the co-localized motion-direction signals induced by adaptation.     

Simple and contingent aftereffects of perceived duration in vision and audition

After repeated presentations of a long inspection tone (800 or 1,000 msec), a test tone of intermediate duration (600 msec) appeared shorter than it would otherwise appear. A short inspection tone (200 or 400 msec) tended to increase the apparent length of the intermediate test tone. Thus, a negative aftereffect of perceived auditory duration occurred, and a similar aftereffect occurred in the visual modality. These aftereffects, each involving a single sensory dimension, aresimple aftereffects. The following procedures producedcontingent aftereffects of perceived duration. A pair of lights, the first short and the second long, was presented repeatedly during an inspection period. When a pair of test lights of intermediate duration was then presented, the first member of the pair appeared longer in relation to the second. A similar aftereffect occurred in the auditory modality. In these latter aftereffects, the perceived duration of a test light or tone is contingent—dependent—on its temporal order, first or second, within a pair of test stimuli. An experiment designed to test the possibility of cross-modal transfer of contingent aftereffects between audition and vision found no significant cross-modal aftereffects.     

Visual motion influences the contingent auditory motion aftereffect

In this study, we show that the contingent auditory motion aftereffect is strongly influenced by visual motion information. During an induction phase, participants listened to rightward-moving sounds with falling pitch alternated with leftward-moving sounds with rising pitch (or vice versa). Auditory aftereffects (i.e., a shift in the psychometric function for unimodal auditory motion perception) were bigger when a visual stimulus moved in the same direction as the sound than when no visual stimulus was presented. When the visual stimulus moved in the opposite direction, aftereffects were reversed and thus became contingent upon visual motion. When visual motion was combined with a stationary sound, no aftereffect was observed. These findings indicate that there are strong perceptual links between the visual and auditory motion-processing systems.     

Children’s representations of facial expression and identity: Identity-contingent expression aftereffects

This investigation used adaptation aftereffects to examine developmental changes in the perception of facial expressions. Previous studies have shown that adults’ perceptions of ambiguous facial expressions are biased following adaptation to intense expressions. These expression aftereffects are strong when the adapting and probe expressions share the same facial identity but are mitigated when they are posed by different identities. We extended these findings by comparing expression aftereffects and categorical boundaries in adults versus 5- to 9-year-olds (n = 20/group). Children displayed adult-like aftereffects and categorical boundaries for happy/sad by 7 years of age and for fear/anger by 9 years of age. These findings suggest that both children and adults perceive expressions according to malleable dimensions in which representations of facial expression are partially integrated with facial identity.     

Contingent aftereffects: lateral interactions between color and motion

A randomly dotted yellow disk was rotated at a speed of 5 rpm, alternating in direction every 10 sec. Its change in direction of rotation was paired with a change in surround color, which was either red or green. After 15 min of exposure, observers reported vivid motion aftereffects contingent on the color of both the stationary disk and the surround, even though during adaptation only motion or color was associated with either alone. In further experiments, it was established that a change in color (or direction of motion) of the disk could be associated with a change in direction of motion (or color) of the surround. Such lateral effects were found even when a wide (5 degree) annulus was introduced between the disk and the surround during adaptation and testing. Furthermore, the aftereffects generalized to the annulus, which was not associated with either color or motion during adaptation. However, when the disk alone was adapted to color and motion, no generalization to the surround was found (and vice versa), suggesting that the effects are not produced by adaptation of large receptive fields or by scatter of light within the eye. The results appear to conflict with the ideas that contingent aftereffects are confined to the adapted area of the retina and that they are built up by links between single-duty neurones, and with an extreme view of the segregation of color and motion early in human vision.     

Spatial inattention abolishes voice adaptation

Adaptation to male voices causes a subsequent voice to be perceived as more female, and vice versa. Similar contrastive aftereffects have been reported for phonetic perception, and in vision for face perception. However, while aftereffects in the perception of phonetic features of speech have been reported to persist even when adaptors were processed inattentively, face aftereffects were previously reported to be abolished by inattention to adaptors. Here we demonstrate that auditory aftereffects of adaptation to voice gender are eliminated when the male and female adaptor voices are spatially unattended. Participants simultaneously heard gender-specific male or female adaptor voices in one ear and gender-neutral (androgynous) adaptor voices in the contralateral ear. They selectively attended to the adaptor voices in a designated ear, by either classifying voice gender (Exp. 1) or spoken syllable (Exp. 2). Voice aftereffects were found only if the gender-specific voices were spatially attended, suggesting capacity limits in the processing of voice gender for the unattended ear. Remarkably, gender-specific adaptors in the attended ear elicited comparable aftereffects in test voices, regardless of prior attention to voice gender or phonetic content. Thus, within the attended ear, voice gender was processed even when it was irrelevant for the task at hand, suggesting automatic processing of gender along with linguistic information. Overall, voice gender adaptation requires spatial, but not dimensional, selective attention.     

Perceptual asymmetries associated with changing-loudness aftereffects

Listening to decreasing sound level leads to an increasing-loudness aftereffect, whereas listening to increasing sound level leads to a decreasing-loudness aftereffect. Measuring the aftereffects by nulling them in short test stimuli reveals that increasing-loudness aftereffects are greater than decreasing-loudness aftereffects. However, this perceptual asymmetry may be due to another illusion--the growing-louder effect: In the absence of any adaptation, short steady stimuli are heard as growing louder. In an experiment in which the duration of test stimuli varied from 1.0 to 2.5 sec, the growing-louder effect did not occur in the longer test stimuli, but the asymmetry in changing-loudness aftereffects remained. The aftereffect asymmetry is therefore independent of the growing-louder effect. The aftereffect asymmetry is consistent with other psychophysical and physiological evidence that is believed to concern potential collision: An approaching sound-source elicits increasing sound level. In addition, the aftereffect asymmetry parallels a well-known asymmetry regarding aftereffects of visual motion, which is also attributed to potential collision.     

数量适应后效的皮层映射特征

本研究探讨了观察者与观察目标存在相对运动时视觉系统对目标数量特征的适应后效的皮层映射特征, 并与对比度适应后效的映射规律进行比较。包括两项实验。其中, 实验一要求被试在适应目标后转换注视点, 考察眼跳后相同和不同视网膜区域以及相同和不同空间区域的适应后效, 发现数量适应后效具有部分空间-皮层映射特性, 而对比度适应后效则表现出完全的视网膜-皮层映射特征。实验二采用固定的注视点, 考察目标运动后目标原位置和新位置区域的适应后效, 发现数量适应后效不完全依赖于视网膜-皮层映射, 它可以“追随”客体运动重新映射到新的位置, 表现出基于客体映射的特征, 而对比度适应后效则完全依赖于视网膜-皮层映射, 不能“追随”客体移动在目标新位置重新形成映射。两项实验结果提示, 相对于对比度等低级表面特征而言, 数量特征对目标的描述涉及更高的加工水平, 它可以与观察目标的相对运动信息进行整合, 且这种整合在眼跳和非眼跳的观察条件下都可发生。     

A motion aftereffect from still photographs depicting motion

A photograph of an action can convey a vivid sense of motion. Does the inference of motion from viewing a photograph involve the same neural and psychological representations used when one views physical motion? In this study, we tested whether implied motion is represented by the same direction-selective signals involved in the perception of real motion. We made use of the motion aftereffect, a visual motion illusion. Three experiments showed that viewing a series of static photographs with implied motion in a particular direction produced motion aftereffects in the opposite direction, as assessed with real-motion test probes. The transfer of adaptation from motion depicted in photographs to real motion demonstrates that the perception of implied motion activates direction-selective circuits that are also involved in processing real motion.     

Text-contingent color aftereffects: A reexamination

Five experiments reexamined color aftereffects contingent on the semantic properties of text (Allan, Siegel, Collins, & MacQueen, 1989). The influence of different assessment techniques and the effect of eye movements and overlapping contour information on the induction of color aftereffects by word and nonword letter strings were determined. Experiment 1 showed that no aftereffect was found when a traditional method of assessing color aftereffects was used. Experiments 2 and 4 demonstrated color aftereffects forboth words and nonwords, but only when subjects fixated the same locus during induction and testing and only when assessed with the technique described by Allan et al. (1989). If, however, eye movements were made during induction, no color aftereffect was obtained (Experiment 3). Induction to nontext patterns with properties similar to those of text but with fewer overlapping contours resulted in a strong color aftereffect (Experiment 5). These results suggest that the color aftereffect contingent on text is very weak and is not dependent on semantic factors, but that it is a product of induction to local color and orientation information.     

Persistence of simple and contingent motion aftereffects

Jones and Holding (1975) showed that orientation-contingent color aftereffects can persist for at least 3 months, but are depleted by repeated testing. We applied the same paradigm to a simple motion aftereffect (MAE) and found that it can persist for up to 1week and is only slightly diminished by testing. It was further found that simple MAEs appear to persist longer than color-contingent MAEs, although when procedures for inducing and measuring both kinds of aftereffect are equalized, contingent MAEs last longer. Finally, no tendency was found for color-contingent MAEs to diminish with repeated testing. Although both simple and color-contingent MAEs can be relatively persistent, there are certain differences between them. Furthermore, contingent aftereffects should not be considered interchangeable, as there appear to be large differences in the persistence of orientation-contingent color aftereffect and color-contingent MAEs.     

Response scatter in measuring changing-loudness aftereffects: evidence for simplified processing of auditory motion-in-depth and potential collision

Researchers have postulated 2 mechanisms for processing auditory motion: a direct mechanism processing motion itself and an indirect mechanism sensitive to location over discrete points in time. Measuring aftereffects of azimuthal motion by nulling entails scattered responding, which is attributed to a conflict between direct and indirect mechanisms. In this experiment, the author obtained nulls following adaptation to changing sound level, a property of approaching or receding sound sources, and for nonadaptation. Test stimuli ranged in duration from 1.0 to 2.5 s. Longer test stimuli evinced reductions in both changing-loudness aftereffects and the associated response scatters. However, the latter matched the nonadaptation response scatters. The author suggests that judging longer test stimuli is easier, so an indirect mechanism need not be invoked. Simplified processing of changing sound level may underlie the rapid responses required for potential collision.     

Motion aftereffects from a motionless stimulus

Dimming or brightening regions superimposed, slightly out of register, on static light or dark blobs, give rise to apparent motion. When these regions are replaced by apparent brightening or dimming produced by ramp aftereffects, a directional motion aftereffect is perceived. It is concluded that filters sensitive to temporal derivative signals of net brightening or dimming provide an input into the motion pathways.     

Monocular-contingent and binocular-contingent aftereffects

Alternate monocular and binocular exposure to complementary stimulation can yield opposite but coexisting aftereffects that are contingent on whether the test display is viewed with one eye or two eyes. The motion aftereffect was studied by adapting each eye separately to a contracting spiral and both eyes together to an expanding spiral. The stationary test spiral subsequently appeared to be expanding when viewed monocularly, but to be contracting when it was seen with both eyes open. With respect to the McCollough effect, after monocular exposure to red-vertical and green-horizontal gratings and binocular exposure to red-horizontal and green-vertical gratings, the appearance of the color of the test gratings when viewed with one eye was different from that when viewed with both eyes. Opposite, coexisting aftereffects induced by complementary stimulation can be interpreted as evidence that there are unique binocular aspects to visual function.