In contrast to speech
intelligibility, speech comprehension entails numerous cognitive activities
such as the integration of the physical speech signal over time and the access
to and selection of appropriate semantic representations using decision
strategies to operate semantic information (Davis & Johnsrude, 2003). Most
studies on speech comprehension showed that extensively spread systems on both
hemispheres are involved in speech comprehension (Benson
et al., 2001; Binder et al., 1997; Chee, O'Craven, Bergida, Rosen, & Savoy,
1999; Demonet et al., 1992; Demonet, Price, Wise, & Frackowiak, 1994a;
Nakai et al., 1999; Newman, Pancheva, Ozawa, Neville, & Ullman, 2001;
Scott, Leff, & Wise, 2003; Spitsyna, Warren, Scott, Turkheimer, & Wise,
2006; Visser, Jefferies, & Lambon Ralph, 2010). Many investigations have
been carried out to uncover the neural basis of speech comprehension (Crinion
& Price, 2005; Humphries, Willard, Buchsbaum, & Hickok, 2001; Obleser
et al., 2007a; Obleser, Eisner, & Kotz, 2008; Peelle et al., 2010). However, most of these
studies focused on comprehension of spoken sentences.
Neuroimaging studies that focussed
on the phonological and semantic processing of words demonstrated that together
with the left parietal angular gyri, the left middle and inferior temporal gyri
are involved in semantic processing while the left posterior inferior gyrus of
the frontal lobe and the supramarginal gyri of the parietal lobe enable
listeners to phonologically resolve sound information of words (Demonet et al.,
1992, 1994a). The observation that those structures that are relevant for
semantically processing auditory words are identical to those that are
important for semantic operations on visually presented words, indicated a
semantic system for words irrespective of presentation mode (Vandenberghe,
Price, Wise, Josephs, & Frackowiak, 1996). This amodal processing of
semantic information, through which broadly distributed temporal, frontal and
parietal regions for speech comprehension of both auditory and visual words are
engaged, has been further supported (Chee et al., 1999; Newman et al., 2001).
Specifically, right frontal and temporal areas have been related to speech
comprehension as well (Newman et al, 2001).
Other speech comprehension studies
showed a stronger involvement of prefrontal and angular gyri when more effort
was required to retrieve semantic associations when sentences in a foreign
language were, for example, presented to listeners (Nakai et al., 1999). While
the determination of word meaning through semantic context has been observed to
elicit activation from the left superior frontal gyrus (Scott et al., 2003), tasks
in which listeners were required to pay particular attention during speech
comprehension was reported to activate the dorsal posterior frontal regions (Giraud et al., 1994). Moreover, the posterior
middle temporal region, which was shown to respond to semantic requirements,
was reported to become more active as executive needs intensified (Whitney, Jefferies,
& Kircher, 2011).
Although the ventral inferior frontal cortex was related to planned semantic
operations (Adams & Janata, 2002; Badre, Poldrack,
Pare-Blagoev, Insler, & Wagner, 2005), similar to the angular gyri and
the left fusiform gyrus, the ventral inferior frontal cortex responded to
elevated difficulty in accessing semantic knowledge when speech was presented in both visual and auditory modes (Adams & Janata,
2002; Rodd, Davis, & Johnsrude, 2005; Schmithorst, Holland, & Plante,
2006; Spitsyna et al., 2006). The angular gyri were related to top-down
processing in forecasting semantic information and to the recovery and
combination of concepts (Binder,
Desai, Graves, & Conant, 2009; Brownsett & Wise, 2010; Obleser &
Kotz, 2010).
More recently, the broadly dispersed
system of semantic representation was suggested to include the posterior
temporoparietal cortex, the precuneus and the left angular gyrus in the
parietal areas, the middle and superior frontal gyri and the left frontal pars
orbitalis as well as the posterior inferior temporal gyrus, the middle temporal
gyrus and the anterior temporal fusiform (Rogalsky,
Matchin, & Hickok, 2008; Visser et al., 2010; Visser & Lambon Ralph,
2011).
Prior research on speech comprehension has reported a considerable overlay of parts
of those structures that are significant for speech articulation, such as the pars
opercularis and triangularis of IFG and the inferior and lateral areas of the
right cerebellar cortex, with those structures that are essential for speech
comprehension (Papathanassiou
et al., 2000). This observation has been suggested
to account for activities that are shared by both articulation and
comprehension of speech and which include processes of for instance articulatory
strategies, short-term auditory memory and semantic processing (Bookheimer, 2002; Papathanassiou et al.,
2000; Wise et al., 2001).
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