没听到？“听”到！——来自听觉表象神经机制研究的证据

近年来听觉表象开始得到关注,相关研究包括言语声音、音乐声音、环境声音的听觉表象三类。本文梳理了认知神经科学领域对上述三种听觉表象所激活的脑区研究,比较了听觉表象和听觉对应脑区的异同,并展望了听觉表象未来的研究方向。     

中央重新定向对听觉返回抑制的影响

采用线索一靶子范式考察听觉中央重新定向对听觉返回抑制的影响。结果表明：1）听觉中央重新定向的有无不是听觉返回抑制产生的关键因素,但它的存在能够较好地引导听觉选择性注意进行快速转移,提高听觉选择性注意的搜索效率;2）听觉中央重新定向对听觉返回抑制量的大小没有显著影响。     

Action enhances auditory but not visual temporal sensitivity

People naturally dance to music, and research has shown that rhythmic auditory stimuli facilitate production of precisely timed body movements. If motor mechanisms are closely linked to auditory temporal processing, just as auditory temporal processing facilitates movement production, producing action might reciprocally enhance auditory temporal sensitivity. We tested this novel hypothesis with a standard temporal-bisection paradigm, in which the slope of the temporal-bisection function provides a measure of temporal sensitivity. The bisection slope for auditory time perception was steeper when participants initiated each auditory stimulus sequence via a keypress than when they passively heard each sequence, demonstrating that initiating action enhances auditory temporal sensitivity. This enhancement is specific to the auditory modality, because voluntarily initiating each sequence did not enhance visual temporal sensitivity. A control experiment ruled out the possibility that tactile sensation associated with a keypress increased auditory temporal sensitivity. Taken together, these results demonstrate a unique reciprocal relationship between auditory time perception and motor mechanisms. As auditory perception facilitates precisely timed movements, generating action enhances auditory temporal sensitivity.     

Experience and information loss in auditory and visual memory

Recent studies show that recognition memory for sounds is inferior to memory for pictures. Four experiments were conducted to examine the nature of auditory and visual memory. Experiments 1–3 were conducted to evaluate the role of experience in auditory and visual memory. Participants received a study phase with pictures/sounds, followed by a recognition memory test. Participants then completed auditory training with each of the sounds, followed by a second memory test. Despite auditory training in Experiments 1 and 2, visual memory was superior to auditory memory. In Experiment 3, we found that it is possible to improve auditory memory, but only after 3 days of specific auditory training and 3 days of visual memory decay. We examined the time course of information loss in auditory and visual memory in Experiment 4 and found a trade-off between visual and auditory recognition memory: Visual memory appears to have a larger capacity, while auditory memory is more enduring. Our results indicate that visual and auditory memory are inherently different memory systems and that differences in visual and auditory recognition memory performance may be due to the different amounts of experience with visual and auditory information, as well as structurally different neural circuitry specialized for information retention.     

Audition dominates vision in duration perception irrespective of salience,attention, and temporal discriminability

Whereas the visual modality tends to dominate over the auditory modality in bimodal spatial perception, the auditory modality tends to dominate over the visual modality in bimodal temporal perception. Recent results suggest that the visual modality dominates bimodal spatial perception because spatial discriminability is typically greater for the visual than for the auditory modality; accordingly, visual dominance is eliminated or reversed when visual-spatial discriminability is reduced by degrading visual stimuli to be equivalent or inferior to auditory spatial discriminability. Thus, for spatial perception, the modality that provides greater discriminability dominates. Here, we ask whether auditory dominance in duration perception is similarly explained by factors that influence the relative quality of auditory and visual signals. In contrast to the spatial results, the auditory modality dominated over the visual modality in bimodal duration perception even when the auditory signal was clearly weaker, when the auditory signal was ignored (i.e., the visual signal was selectively attended), and when the temporal discriminability was equivalent for the auditory and visual signals. Thus, unlike spatial perception, where the modality carrying more discriminable signals dominates, duration perception seems to be mandatorily linked to auditory processing under most circumstances.     

Anesthesia and the electrophysiology of auditory consciousness

Empirical work is reviewed which correlates the presence or absence of various parts of the auditory evoked potential with the disappearance and reemergence of auditory sensation during induction of and recovery from anesthesia. As a result, the hypothesis is generated that the electrophysiological correlate of auditory sensation is whatever neural activity generates the middle latency waves of the auditory evoked potential. This activity occurs from 20 to 80 ms poststimulus in the primary and secondary areas of the auditory cortex. Evidence is presented suggesting that earlier or later waves in the auditory evoked potential do not covary with auditory sensation (as opposed to auditory perception) and it is therefore suggested that they are possibly not the electrophysiological correlates of sensation.     

Echoic and retrieval accounts of the long-term modality effect tested using the suffix procedure

The long-term modality effect is the advantage in recall of the last of a list of auditory to-be-remembered (TBR) items compared with the last of a list of visual TBR items when the list is followed by a filled retention interval. If the auditory advantage is due to echoic sensory memory mechanisms, then recall of the last auditory TBR item should be substantially reduced when it is followed by a redundant, not-to-be-recalled auditory suffix. Contrary to this prediction, Experiment 1 demonstrated that a redundant auditory suffix does not significantly reduce recall of the last auditory TBR item. In Experiment 2 a nonredundant auditory suffix produced a large reduction in the last auditory item. Redundancy is not the only factor controlling the effectiveness of a suffix, however. Experiment 3 demonstrated that a nonredundant visual suffix does not reduce recall of the last auditory TBR item. These results are discussed in reference to a retrieval account of the long-term modality effect.     

A systematic investigation of same and cross modality priming using written and spoken responses

Effects of presentation modality and response format were investigated using visual and auditory versions of the word stem completion task. Study presentation conditions (visual, auditory, non-studied) were manipulated within participants, while test conditions (visual/written, visual/spoken, auditory/written, auditory/spoken, recall-only) were manipulated between participants. Results showed evidence for same modality and cross modality priming on all four word stem completion tasks. Words from the visual study list led to comparable levels of priming across all test conditions. In contrast, words from the auditory study list led to relatively low levels of priming in the visual/written test condition and high levels of priming in the auditory/spoken test condition. Response format was found to influence priming performance following auditory study in particular. The findings confirm and extend previous research and suggest that, for implicit memory studies that require auditory presentation, it may be especially beneficial to use spoken rather than written responses.     

Change perception in complex auditory scenes

In four experiments, we examined the role of auditory transients and auditory short-term memory in perceiving changes in a complex auditory scene comprising multiple auditory objects. Participants were presented pairs of complex auditory scenes that were composed of a maximum of four animal calls delivered in free field; participants were instructed to decide whether the two scenes were the same or different (Experiments 1, 2, and 4). Changes to the second scene consisted of either the addition or the deletion of one animal call. Contrary to intuitive predictions based on results from the visual change blindness literature, substantial deafness to the change emerged without regard to whether the scenes were separated by 500 msec of masking white noise or by 500 msec of silence (Experiment 1). In fact, change deafness was not even modulated by having the two scenes presented contiguously (i.e., 0-msec interval) or separated by 500 msec of silence (Experiments 2 and 4). This result suggests that change-related auditory transients played little or no role in change detection in complex auditory scenes. Instead, the main determinant of auditory change perception (and auditory change deafness) appears to have been the capacity of auditory short-term memory (Experiments 3 and 4). Taken together, these findings indicate that the intuitive parallels between visual and auditory change perception should be reconsidered.     

Cortical auditory disorder caused by bilateral strategic cerebral bleedings. Analysis of two cases

The authors present the anatomical and clinical features of cortical auditory dysfunction in two patients, in whom hypertensive bleedings destroyed the cortical auditory centres in both hemispheres. The second haemorrhage occurred four years after the first bleeding in both cases. The bleedings isolated the cortical hearing centres due to the destruction of the right and left temporal white matter. During the clinical course the symptomatology has changed in both patients: pure word deafness has transformed to cortical deafness and generalised auditory agnosia. Normal pattern of brain stem auditory evoked potentials suggested intact auditory pathways. Authors conclude that transformation of clinical forms of cortical auditory disorder can be explained by the tissue reaction to the subcortical bleeding in the cortical auditory centres.     

A two-stage model for visual-auditory interaction in saccadic latencies

In two experiments, saccadic response time (SRT) for eye movements toward visual target stimuli at different horizontal positions was measured under simultaneous or near-simultaneous presentation of an auditory nontarget (distractor). The horizontal position of the auditory signal was varied, using a virtual auditory environment setup. Mean SRT to a visual target increased with distance to the auditory nontarget and with delay of the onset of the auditory signal relative to the onset of the visual stimulus. A stochastic model is presented that distinguishes a peripheral processing stage with separate parallel activation by visual and auditory information from a central processing stage at which intersensory integration takes place. Two model versions differing with respect to the role of the auditory distractors are tested against the SRT data.     

Towards a rich view of auditory experience

In this paper I will argue that the gender properties expressed by human voices are part of auditory phenomenology. I will support this claim by investigating auditory adaptational effects on such properties and contrasting auditory experiences, before and after the adaptational effects take place. In light of this investigation, I will conclude that auditory experience is not limited to low-level properties. Perception appears to be much more informative about the auditory landscape than is commonly thought.     

Musicians experience less age-related decline in central auditory processing

Age-related decline in auditory perception reflects changes in the peripheral and central auditory systems. These age-related changes include a reduced ability to detect minute spectral and temporal details in an auditory signal, which contributes to a decreased ability to understand speech in noisy environments. Given that musical training in young adults has been shown to improve these auditory abilities, we investigated the possibility that musicians experience less age-related decline in auditory perception. To test this hypothesis we measured auditory processing abilities in lifelong musicians (N = 74) and nonmusicians (N = 89), aged between 18 and 91. Musicians demonstrated less age-related decline in some auditory tasks (i.e., gap detection and speech in noise), and had a lifelong advantage in others (i.e., mistuned harmonic detection). Importantly, the rate of age-related decline in hearing sensitivity, as measured by pure-tone thresholds, was similar between both groups, demonstrating that musicians experience less age-related decline in central auditory processing.     

Auditory free classification: Methods and analysis

The free classification paradigm and its potential application to perceptual acoustic and auditory research are summarized. Specific methods for the application of the auditory free classification paradigm in speech research are then described, including techniques for stimulus preparation, data collection, and statistical analysis, based on a sample auditory free classification study of regional dialect variation. The results suggest that auditory free classification is a promising paradigm for examining the perceptual classification and similarity of speech and nonspeech auditory stimulus materials.     

Auditory imagery and the poor-pitch singer

The vocal imitation of pitch by singing requires one to plan laryngeal movements on the basis of anticipated target pitch events. This process may rely on auditory imagery, which has been shown to activate motor planning areas. As such, we hypothesized that poor-pitch singing, although not typically associated with deficient pitch perception, may be associated with deficient auditory imagery. Participants vocally imitated simple pitch sequences by singing, discriminated pitch pairs on the basis of pitch height, and completed an auditory imagery self-report questionnaire (the Bucknell Auditory Imagery Scale). The percentage of trials participants sung in tune correlated significantly with self-reports of vividness for auditory imagery, although not with the ability to control auditory imagery. Pitch discrimination was not predicted by auditory imagery scores. The results thus support a link between auditory imagery and vocal imitation.     

Visual and auditory processing of common pattern class structure

Visual and auditory classification of equivalent class structured patterns were examined. Underlying patterns from two classes were translated into auditory tone sequences and visual polygons. All Ss classified 50 visual patterns and their direct auditory analogs. Visual classification accuracy exceeded auditory accuracy (p < .01); however, auditory accuracy improved when auditory classification was preceded by the visual task (p < .01). Based on group data, classification strategies appeared similar across modalities, with accuracy of classification of individual patterns predicted to the same degree by common measures of physical class structure across modalities. Ss’ drawings of the prototypes also suggested a common strategy across modalities. While group data suggest some consistency of classification strategy across modalities, individual Ss were not at all consistent in their visual and auditory classifications.     

Switching in the cocktail party: exploring intentional control of auditory selective attention

Using a novel variant of dichotic selective listening, we examined the control of auditory selective attention. In our task, subjects had to respond selectively to one of two simultaneously presented auditory stimuli (number words), always spoken by a female and a male speaker, by performing a numerical size categorization. The gender of the task-relevant speaker could change, as indicated by a visual cue prior to auditory stimulus onset. Three experiments show clear performance costs with instructed attention switches. Experiment 2 varied the cuing interval to examine advance preparation for an attention switch. Experiment 3 additionally isolated auditory switch costs from visual cue priming by using two cues for each gender, so that gender repetition could be indicated by a changed cue. Experiment 2 showed that switch costs decreased with prolonged cuing intervals, but Experiment 3 revealed that preparation did not affect auditory switch costs but only visual cue priming. Moreover, incongruent numerical categories in competing auditory stimuli produced interference and substantially increased error rates, suggesting continued processing of task-relevant information that often leads to responding to the incorrect auditory source. Together, the data show clear limitations in advance preparation of auditory attention switches and suggest a considerable degree of inertia in intentional control of auditory selection criteria.     

早期听觉剥夺后的大脑可塑性：来自先天性听力障碍群体的证据

皮层功能的正常发展依赖于充分的外部感觉信息的输入。先天性听力障碍群体由于经历早期听觉剥夺, 皮层功能往往出现异常。具体表现为初级听皮层功能退化, 初级、次级听皮层的功能连接变弱, 次级听皮层出现跨通道功能重组; 在后天听力重建后听皮层功能重组仍然存在, 言语加工需要更多高级认知资源的补偿。已有研究在探讨听力重建后皮层的长期可塑性机制、复杂声学环境下言语加工机制、汉语言加工独特性等方面尚不深入, 值得进一步研究。     

Monaural Auditory Cue Affects the Process of Choosing the Initial Swing Leg in Gait Initiation

The authors investigated the effect of an auditory cue on the choice of the initial swing leg in gait initiation. Healthy humans initiated a gait in response to a monaural or binaural auditory cue. When the auditory cue was given in the ear ipsilateral to the preferred leg side, the participants consistently initiated their gait with the preferred leg. In the session in which the side of the monaural auditory cue was altered trial by trial randomly, the probability of initiating the gait with the nonpreferred leg increased when the auditory cue was given in the ear contralateral to the preferred leg side. The probability of choosing the nonpreferred leg did not increase significantly when the auditory cue was given in the ear contralateral to the preferred leg side in the session in which the auditory cue was constantly given in the ear contralateral to the preferred leg side. The reaction time of anticipatory postural adjustment was shortened, but the probability of choosing the nonpreferred leg was not significantly increased when the gait was initiated in response to a binaural auditory cue. An auditory cue in the ear contralateral to the preferred leg side weakens the preference for choosing the preferred leg as the initial swing leg in gait initiation when the side of the auditory cue is unpredictable.     

A comparison of higher order auditory processes in younger and older adults

The authors conducted 3 experiments investigating the effects of aging on higher order auditory processes. They compared younger and older adults with respect to (a) their auditory channel capacity, (b) the extent of their top-down control over auditory gain, and (c) their ability to focus attention on a narrow band of frequencies. To ensure that subclinical cochlear processing deficits in older adults (e.g., higher thresholds, poorer discrimination of frequency and intensity differences) did not limit performance, the authors used only stimuli that were perfectly discriminable by all participants. No age differences were found in any of these experiments, suggesting that some higher order auditory processes (e.g., top-down control over auditory gain, auditory attention) are preserved in normal aging, despite numerous age-related declines in peripheral auditory functionality.