Decoding lexical tones and vowels in imagined tonal monosyllables using fNIRS signals

Abstract Objective. Speech is a common way of communication. Decoding verbal intent could provide a naturalistic communication way for people with severe motor disabilities. Active brain computer interaction (BCI) speller is one of the most commonly used speech BCIs. To reduce the spelling time of Chinese words, identifying vowels and tones that are embedded in imagined Chinese words is essential. Functional near-infrared spectroscopy (fNIRS) has been widely used in BCI because it is portable, non-invasive, safe, low cost, and has a relatively high spatial resolution. Approach. In this study, an active BCI speller based on fNIRS is presented by covertly rehearsing tonal monosyllables with vowels (i.e. /a/, /i/, /o/, and /u/) and four lexical tones in Mandarin Chinese (i.e. tones 1, 2, 3, and 4) for 10 s. Main results. fNIRS results showed significant differences in the right superior temporal gyrus between imagined vowels with tone 2/3/4 and those with tone 1 (i.e. more activations and stronger connections to other brain regions for imagined vowels with tones 2/3/4 than for those with tone 1). Speech-related areas for tone imagery (i.e. the right hemisphere) provided majority of information for identifying tones, while the left hemisphere had advantages in vowel identification. Having decoded both vowels and tones during the post-stimulus 15 s period, the average classification accuracies exceeded 40% and 70% in multiclass (i.e. four classes) and binary settings, respectively. To spell words more quickly, the time window size for decoding was reduced from 15 s to 2.5 s while the classification accuracies were not significantly reduced. Significance. For the first time, this work demonstrated the possibility of discriminating lexical tones and vowels in imagined tonal syllables simultaneously. In addition, the reduced time window for decoding indicated that the spelling time of Chinese words could be significantly reduced in the fNIRS-based BCIs.