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阅读障碍者对次音位片段的敏感性增强:音位变体感知的一个新例证。

Enhanced Sensitivity to Subphonemic Segments in Dyslexia: A New Instance of Allophonic Perception.

作者信息

Serniclaes Willy, Seck M'ballo

机构信息

Speech Perception Lab., CNRS & Paris Descartes University, 75006 Paris, France.

Human & Artificial Cognition Lab., Paris 8 University, 93526 Saint-Denis, France.

出版信息

Brain Sci. 2018 Mar 26;8(4):54. doi: 10.3390/brainsci8040054.

Abstract

Although dyslexia can be individuated in many different ways, it has only three discernable sources: a visual deficit that affects the perception of letters, a phonological deficit that affects the perception of speech sounds, and an audio-visual deficit that disturbs the association of letters with speech sounds. However, the very nature of each of these core deficits remains debatable. The phonological deficit in dyslexia, which is generally attributed to a deficit of phonological awareness, might result from a specific mode of speech perception characterized by the use of allophonic (i.e., subphonemic) units. Here we will summarize the available evidence and present new data in support of the "allophonic theory" of dyslexia. Previous studies have shown that the dyslexia deficit in the categorical perception of phonemic features (e.g., the voicing contrast between /t/ and /d/) is due to the enhanced sensitivity to allophonic features (e.g., the difference between two variants of /d/). Another consequence of allophonic perception is that it should also give rise to an enhanced sensitivity to allophonic segments, such as those that take place within a consonant cluster. This latter prediction is validated by the data presented in this paper.

摘要

尽管诵读困难可以通过多种不同方式来鉴别,但它只有三个可辨别的根源:一种影响字母感知的视觉缺陷、一种影响语音感知的语音缺陷,以及一种干扰字母与语音关联的视听缺陷。然而,这些核心缺陷中每一个的本质仍存在争议。诵读困难中的语音缺陷通常归因于语音意识的缺陷,它可能源于一种以使用音位变体(即次音位)单元为特征的特定语音感知模式。在此,我们将总结现有证据并呈现新数据,以支持诵读困难的“音位变体理论”。先前的研究表明,诵读困难在音位特征的范畴感知方面(例如 /t/ 和 /d/ 之间的浊音对比)的缺陷,是由于对音位变体特征(例如 /d/ 的两个变体之间的差异)的敏感性增强。音位变体感知的另一个结果是,它也应该会导致对音位变体系段(例如那些出现在辅音群中的音位变体系段)的敏感性增强。本文所呈现的数据验证了后一个预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e2f/5924390/292a66765d5d/brainsci-08-00054-g001.jpg

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