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. 2016 Sep 21;10:435. doi: 10.3389/fnhum.2016.00435

Table 1.

Overview of functional magnetic resonance imaging (fMRI) studies investigating involvement of inferior frontal, sensorimotor and inferior parietal systems in syllable perception.

No. Study Stimuli features investigated Phonetic Task Button presses Sparse imaging Analyses Baseline Activation/Decoding found in …
Prefrontal areas Motor areas Somatosensory and inferior parietal areas
1 Benson et al. (2001) 15 C/VC/CVC syllables n/a none never yes univariate non-speech tones left BA 9, 10 left BA 6 left SMG (BA 40)
2 Wilson et al. (2004) /pa/, /gi/ n/a none never no univariate rest/silence not reported ventral (v) BA 4, 6 right SMG (BA 40)
3 Wilson and Iacoboni (2006) 50 consonants embedded between two /α/ vowels n/a none never no univariate rest/silence not reported v BA 4, 6 not reported
4 Szenkovits et al. (2012) monosyllabic pseudowords n/a one-back repetition detection task 10% of trials no univariate non-speech buzzes not reported not reportedd not reported
5 Grabski et al. (2013) 9 vowels n/a none never yes univariate rest/silence BA 44, left BA 45 right BA 6 not reported
6 Pulvermüller et al. (2006) /pæ/, /tæ/, /pI/, /tI/ Place none never yes univariate, ROI-baseda matched noise stimuli not reported left v BA 4, 6 (differential activation of lip vs. tongue regions) not reported
7 Raizada and Poldrack (2007) /ba/, /da/ Place detect occasional quieter stimulus 6% of trials yes repetition adaptation n/a left middle frontal cortex (amplification of response to stimulus pairs differing in place) not reported left SMG (amplification of response to stimulus pairs differing in place)
8 Myers et al. (2009) /da/, /ta/ Voicing detect occasional high-pitched stimulus 37.5% of trials yes repetition adaptation n/a left inferior frontal sulcus (release from adaptation only for stimuli differing in voicing) not reported not reported
9 Lee et al. (2012) 10 CV syllables on /ba/-/da/ continuum Place detect occasional quieter stimulus 11% of trials yes MVPA (searchlight) n/a left BA 44 (decoding of place) left pre-SMA (decoding of place) not reported
10 Chevillet et al. (2013)b /da/–/ga/ continuum Place dichotic listening (detect in which ear the sound persisted longer) always yes repetition adaptation n/a not reported left BA 6 (release from adaptation for stimulus pairs differing in place of articulation) not reported
11 Du et al. (2014) /ba/, /ma/, /da/, /ta/ Place active syllable identification (4-AFC) always no (but scanner noise attenuation by 25 dB) MVPA (searchlight) n/a Insula/Broca’s area (decoding of place)—at low/moderate noise levels onlye left v BA 6 (decoding of place)—at low noise levels onlyf left inferior parietal lobule (decoding of place)—at low noise levels only
12 Arsenault and Buchsbaum (2015) 16 CV syllables Place, manner, voicing gender identification task always no MVPA (ROI-based) n/a not reported not reported left subcentral gyrus (decoding of place)
13 Evans and Davis (2015) /ba/, /da/, /ma/, /na/, /ab/, /ad/ Place, manner, phoneme identity, CV structure (CV vs. VC) one-back repetition detection task 8% of trials yes MVPA-based RSA (searchlight)c rest/silence not reported left precentral gyrus (decoding of syllable and phoneme identity and CV structure) left postcentral gyrus (decoding of syllable identity)
14 Correia et al. (2015) 24 CV syllables Place, manner, voicing none never yes MVPA (searchlight) n/a IFG (decoding of place/manner) right inferior precentral gyrus (decoding of place) postcentral gyrus, SMG (decoding of place/manner)
15 Arsenault and Buchsbaum (2016) 8 CV syllables: /ba/, /pa/, /va/, /fa/, /da/, /ta/, /za/, /sa/ Place (manner/voicing not analyzed) detect occasional blank trials 11% of trials no univariate and MVPA (both ROI-based) n/a not reported not reported left postcentral gyrus (decoding of place)

aDifferential activation of subregions (lip vs. tongue) in left BA 4, 6 depending on place of articulation (lip vs. tongue; see Figure 2 Top). bSee also Alho et al. (2016) for similar results from MEG. cRepresentational similarity analysis (RSA) used to disentangle acoustic and phonological similarity. dNot reported in whole-brain analysis; but note that in a ROI-based analysis a correlation between working memory abilities and motor/premotor activation in speech perception was found. fIn dorsal BA 6 (PMC) decoding was still observed at higher noise levels (see Figure 3), but this might reflect classification of responses rather than speech perception (see main text for discussion). eDue to the active identification task on every trial, this might reflect decision-related processes or response selection/preparation (see main text for discussion).