Song and speech: brain regions involved with perception and covert production
Abstract
This 3-T fMRI study investigates brain regions similarly and differentially involved with listening and covert production of singing relative to speech. Given the greater use of auditory-motor self-monitoring and imagery with respect to consonance in singing, brain regions involved with these processes are predicted to be differentially active for singing more than for speech. The stimuli consisted of six Japanese songs. A block design was employed in which the tasks for the subject were to listen passively to singing of the song lyrics, passively listen to speaking of the song lyrics, covertly sing the song lyrics visually presented, covertly speak the song lyrics visually presented, and to rest. The conjunction of passive listening and covert production tasks used in this study allow for general neural processes underlying both perception and production to be discerned that are not exclusively a result of stimulus induced auditory processing nor to low level articulatory motor control. Brain regions involved with both perception and production for singing as well as speech were found to include the left planum temporale/superior temporal parietal region, as well as left and right premotor cortex, lateral aspect of the VI lobule of posterior cerebellum, anterior superior temporal gyrus, and planum polare. Greater activity for the singing over the speech condition for both the listening and covert production tasks was found in the right planum temporale. Greater activity in brain regions involved with consonance, orbitofrontal cortex (listening task), subcallosal cingulate (covert production task) were also present for singing over speech. The results are consistent with the PT mediating representational transformation across auditory and motor domains in response to consonance for singing over that of speech. Hemispheric laterality was assessed by paired t tests between active voxels in the contrast of interest relative to the left-right flipped contrast of interest calculated from images normalized to the left-right reflected template. Consistent with some hypotheses regarding hemispheric specialization, a pattern of differential laterality for speech over singing (both covert production and listening tasks) occurs in the left temporal lobe, whereas, singing over speech (listening task only) occurs in right temporal lobe.
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The pars opercularis (Broca's area, BA 44) is associated with forming or dividing words into syllables (syllabification) during both covert and overt production.
“The opercular part of the posterior inferior frontal cortex (pars opercularis, Broca's area, BA 44) was associated with forming or dividing words into syllables (syllabification) during both covert (silent speech) and overt (speaking aloud) production (Indefrey and Levelt, 2004; Callan et al., 2006) or translating speech into articulatory code (Hickok and Poeppel, 2004).”
From A review and synthesis of the first 20years of PET and fMRI studies of heard speech, spoken language and reading (2012) · cites this paper as Callan et al., 2006
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- Authors
- Callan, D. E., Tsytsarev, V., Hanakawa, T., Callan, A. M., Katsuhara, M., Fukuyama, H., & Turner, R.
- Affiliations
- Advanced Telecommunications Research Institute International (JP)
- Kyoto University (JP)
- UCL Queen Square Institute of Neurology (GB)
- Corresponding author
- Callan, Daniel E.
- ORCID
- Venue
- NeuroImage
- Publisher
- Elsevier BV
- Published
- 2006-07
- Volume
- 31
- Issue
- 3
- Pages
- 1327-1342
- ISSN
- 1053-8119 (ISSN-L)
- OpenAlex
- W2115780852
- Cited by
- 287
- References
- 86
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 8 · 2023: 17 · 2022: 12 · 2021: 13 · 2020: 15 · 2019: 14 · 2018: 8 · 2017: 13 · 2016: 15 · 2015: 12 · 2014: 18 · 2013: 15 · 2012: 22
- FWCI
- 7.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- NeuroImage (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Digital Library (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- National Institute of Information and Communications Technology
- Wellcome Trust
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neurobiology of Language and Bilingualism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Developmental Biology › Animal Vocal Communication and Behavior
- Keywords
- singing, speech perception, auditory-motor integration, consonance, auditory imagery, planum temporale, hemispheric lateralization, orbitofrontal cortex, subcallosal cingulate, Japanese songs
- MeSH terms
- Adult, Auditory Perception, Brain, Brain Mapping, Cerebellum, Cerebral Cortex, Dominance, Cerebral, Female, Gyrus Cinguli, Humans, Image Processing, Computer-Assisted, Imagination, Magnetic Resonance Imaging, Male, Middle Aged, Music, Nerve Net, Practice, Psychological, Speech, Speech Perception, Temporal Lobe, Voice, Imaging, Three-Dimensional
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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