The time course of auditory and language-specific mechanisms in compensation for sibilant assimilation

Attention, Perception, & Psychophysics - Models of spoken-word recognition differ on whether compensation for assimilation is language-specific or depends on general auditory processing....     

The time course of attention in a simple auditory detection task

What is the time course of human attention in a simple auditory detection task? To investigate this question, we determined the detectability of a 20-msec, 1000-Hz tone presented at expected and unexpected times. Twelve listeners who expected the tone to occur at a specific time after a 300-msec narrowband noise rarely detected signals presented 150-375 msec before or 100-200 msec after that expected time. The shape of this temporal-attention window depended on the expected presentation time of the tone and the temporal markers available in the trials. Further, though expecting the signal to occur in silence, listeners often detected signals presented at unexpected times during the noise. Combined with previous data, these results further clarify the listening strategy humans use when trying to detect an expected sound: Humans seem to listen specifically for that sound, while ignoring the background in which it is presented, around the time when the sound is expected to occur.     

The time course of neural changes underlying auditory perceptual learning

Improvement in perception takes place within the training session and from one session to the next. The present study aims at determining the time course of perceptual learning as revealed by changes in auditory event-related potentials (ERPs) reflecting preattentive processes. Subjects were trained to discriminate two complex auditory patterns in a single session. ERPs were recorded just before and after training, while subjects read a book and ignored stimulation. ERPs showed a negative wave called mismatch negativity (MMN)—which indexes automatic detection of a change in a homogeneous auditory sequence—just after subjects learned to consciously discriminate the two patterns. ERPs were recorded again 12, 24, 36, and 48 h later, just before testing performance on the discrimination task. Additional behavioral and neurophysiological changes were found several hours after the training session: an enhanced P2 at 24 h followed by shorter reaction times, and an enhanced MMN at 36 h. These results indicate that gains in performance on the discrimination of two complex auditory patterns are accompanied by different learning-dependent neurophysiological events evolving within different time frames, supporting the hypothesis that fast and slow neural changes underlie the acquisition of improved perception.     

Coping with phonological assimilation in speech perception: evidence for early compensation

The pronunciation of the same word may vary considerably as a consequence of its context. The Dutch word tuin (English, garden) may be pronounced tuim if followed by bank (English, bench), but not if followed by stoel (English, chair). In a series of four experiments, we examined how Dutch listeners cope with this context sensitivity in their native language. A first word identification experiment showed that the perception of a word-final nasal depends on the subsequent context. Viable assimilations, but not unviable assimilations, were often confused perceptually with canonical word forms in a word identification task. Two control experiments ruled out the possibility that this effect was caused by perceptual masking or was influenced by lexical top-down effects. A passive-listening study in which electrophysiological measurements were used showed that only unviable, but not viable, phonological changes elicited a significant mismatch negativity. The results indicate that phonological assimilations are dealt with by an early prelexical mechanism.     

Inhibitory mechanisms of attention in identification and localization tasks: time course and disruption.

It has been proposed that 1 component of the mechanism of visual selective attention is active inhibition of distracting information. A series of studies examines the time course of inhibition and the possible interfering effects of other task demands. Results demonstrate that inhibition can last at least 7 s after selection processes and that it is unaffected by predictable, unrelated intervening events. However, intervening events that are less predictable, or are the same as the inhibited stimulus, disrupt inhibition. Such results motivate a reconsideration of the previous view of distractor inhibition as a transient, fragile phenomenon.     

The ups and downs of social comparison: mechanisms of assimilation and contrast

Social comparisons influence self-evaluations in multiple ways. Sometimes self-evaluations are assimilated toward a given standard. At other times, they are contrasted away from the standard. On the basis of the selective accessibility model (T. Mussweiler, 2003a), the authors hypothesized that assimilation results if judges engage in the comparison process of similarity testing and selectively focus on similarities to the standard, whereas contrast occurs if judges engage in dissimilarity testing and selectively focus on differences. If these alternative comparison mechanisms are indeed at play, then assimilative and contrastive social comparisons should be accompanied by diverging informational foci on similarities versus differences. Results of 5 studies support this reasoning, demonstrating that assimilation results under conditions that foster similarity testing, whereas contrast occurs under conditions that foster dissimilarity testing. Furthermore, assimilative social comparisons are accompanied by a general informational focus on similarities, whereas contrastive comparisons are accompanied by a focus on differences.     

Errors in auditory direction-finding after compensation for visual re-arrangement

Ss walked about out of doors wearing laterally displacing prisms, and sound-attenuating muffs. Errors occurred in an auditory localization task during exposure to visual displacement. With continued exposure these errors tended to disappear after about 108 min. The errors disappeared earlier when muffs were not worn.     

The time course of prepration

The time course of the adjustments triggered by a warning signal was studied by measuring choice reaction times (RTs) at different predictable foreperiods after such a signal. Before the warning signal, a high time uncertainty situation was created by imposing either a long constant foreperiod of 5 sec. or one varying in the range 1.5 to 5 sec. The warning signal was a click. Foreperiods ranging from 0 to 300 millisec. were used in different blocks of trials. The stimulus was the onset of one of two lamps calling for the pressing of one of two keys. A control condition, without click, was used also. RTs were found to decrease continuously when the forperiod was increased from 0 to 100-150 millisec. The click delivered simultaneously with the stimulus permitted reactions significantly faster than in the control condition. It is concluded (a) that the latency of preparation can be much shorter than the 2 to 4 sec. reported by Woodrow; (b) that the warning signal can be used as a time cue to start preparatory adjustments without starting a refractory period of the order of magnitude found in experiments with pairs of successive reactions, and thus that such refractory periods are not the inevitable cost of paying attention to a signal. There is also some suggestion that in this situation the click not only triggers preparatory adjustments, but also causes an immediate facilitation of the reaction to the visual stimulus.     

语言产生中词频效应老化的神经基础与时间进程

词频效应指语言产生中人们对高频词汇的加工比低频词汇更快更准确的一种现象,它可能发生在语言产生中的不同阶段。对青年人和老年人词频效应的不同特点和加工机制进行比较,可以考察语言产生的认知老化机制。通过语言产生理论可对词频效应的老化进行预测,提出词频效应在个体发展和老化阶段的相对稳定性,分析老化导致词频效应相关的神经基础和加工时间进程的改变。未来研究可进一步分离词频效应与习得年龄效应对语言产生老化的影响,并扩展至神经退行性疾病患者中。     

The time course of visual afterimages: data and theory

Sequential viewing of two orthogonally related patterns produces an afterimage of the first pattern (Vidyasagar et al, 1999 Nature 399 422-423; Francis and Rothmayer, 2003 Perception and Psychophysics 65 508-522). We investigated how the timing between the first stimulus (a vertical bar grating) and the second stimulus (a horizontal bar grating) affected the visibility of the afterimage (a perceived vertical grating). As the duration from offset of the first stimulus increased, reports of afterimages decreased. Holding fixed the total time from offset of the first stimulus and increasing the duration from offset of the second stimulus while decreasing the time between the first and second stimuli, caused a decrease in afterimage reports. We interpret this finding in terms of Grossberg's BCS - FCS (boundary contour system--feature contour system) theory. In this theory, the afterimage percept is the result of color complement after-responses in the FCS system interacting with orientation after-responses in the BCS system. The two types of after-responses interact at a stage of neural filling-in to produce the afterimage percept. As the duration between the stimuli increases, the color after-responses weaken so that visible filling-in is less likely to occur. A similar effect occurs for the orientation after-responses but at a faster time scale. Simulations of the model match the experimental data.     

Visual prediction: psychophysics and neurophysiology of compensation for time delays

A necessary consequence of the nature of neural transmission systems is that as change in the physical state of a time-varying event takes place, delays produce error between the instantaneous registered state and the external state. Another source of delay is the transmission of internal motor commands to muscles and the inertia of the musculoskeletal system. How does the central nervous system compensate for these pervasive delays? Although it has been argued that delay compensation occurs late in the motor planning stages, even the earliest visual processes, such as phototransduction, contribute significantly to delays. I argue that compensation is not an exclusive property of the motor system, but rather, is a pervasive feature of the central nervous system (CNS) organization. Although the motor planning system may contain a highly flexible compensation mechanism, accounting not just for delays but also variability in delays (e.g., those resulting from variations in luminance contrast, internal body temperature, muscle fatigue, etc.), visual mechanisms also contribute to compensation. Previous suggestions of this notion of "visual prediction" led to a lively debate producing re-examination of previous arguments, new analyses, and review of the experiments presented here. Understanding visual prediction will inform our theories of sensory processes and visual perception, and will impact our notion of visual awareness.     

Normal time course of auditory recognition in schizophrenia, despite impaired precision of the auditory sensory ("echoic") memory code

Prior studies have demonstrated impaired precision of processing within the auditory sensory memory (ASM) system in schizophrenia. This study used auditory backward masking to evaluate the degree to which such deficits resulted from impaired overall precision versus premature decay of information within the short-term auditory store. ASM performance was evaluated in 14 schizophrenic participants and 16 controls. Schizophrenic participants were severely impaired in their ability to match tones following delay. However, when no-mask performance was equated across participants, schizophrenic participants were no more susceptible to the effects of backward maskers than were controls. Thus, despite impaired precision of ASM performance, schizophrenic participants showed no deficits in the time course over which short-term representations could be used within the ASM system.     

The time course of competition for attention: attention is initially labile

Competition for attention between 2 written words was investigated by presenting the words briefly in a single stream of distractors (Experiment 1) or in different streams (Experiment 2-6), using rapid serial visual presentation at 53 ms/item. Stimulus onset asynchrony (SOA) was varied from 0 to 213 ms. At all SOAs there was strong competition, but which word was more likely to be reported shifted markedly with SOA. At SOAs in the range of 13-53 ms the second word was more likely to be reported, but at 213 ms, the advantage switched to the first word, as in the attentional blink. A 2-stage competition model of attention is proposed in which attention to a detected target is labile in Stage 1. Stage 1 ends when one target is identified, initiating a serial Stage 2 process of consolidation of that target.     

The time course of object encoding

Four experiments examined the effects of encoding time on object identification priming and recognition memory. After viewing objects in a priming phase, participants identified objects in a rapid stream of non-object distracters; display times were gradually increased until the objects could be identified (Experiments 1-3). Participants also made old/new recognition judgments about previously viewed objects (Experiment 4). Reliable priming for object identification occurred with 150 ms of encoding and reached a maximum after about 300 ms of encoding time. In contrast, reliable recognition judgments occurred with 75 ms of encoding and continued to improve for encoding times of up to 1200 ms. These results suggest that recognition memory may be based on multiple levels of object representation, from rapidly activated representations of low-level features to semantic knowledge associated with the object. In contrast, priming in this object identification task may be tied specifically to the activation of representations of object shape.     

The time course of figure-ground reversal

We report the results from five experiments employing a modified version of the short-term visual matching (STVM) method introduced by Driver and Baylis (1996). In STVM, participants see a study display with ambiguous figure-ground relations. After the study display, participants have to decide which of two shapes in a match display was seen before in the study display. STVM has been used by Vecera, Vogel, and Woodman (2002) to demonstrate that the lower region is a figure-ground cue. In our modified version of STVM, the study stimulus was preceded by a brief prime. This caused a biasing of the figural interpretation of the ambiguous figure-ground displays that contained the lower region cue. We show that 100-msec priming with an unambiguous display is enough to affect the subsequent interpretation of the ambiguous figure-ground display. It takes maximally 350 msec to complete a transition from the nondominant interpretation to the dominant interpretation of an ambiguous figure-ground display that contains the lower region cue.