Neural Correlates of Processing Syntax in Music and ... - PubMan
Neural Correlates of Processing Syntax in Music and ... - PubMan
Neural Correlates of Processing Syntax in Music and ... - PubMan
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<strong>Music</strong> Perception 5<br />
to her <strong>in</strong>fant relative to a comparable performance with no <strong>in</strong>fant audience (Tra<strong>in</strong>or,<br />
1996). Men’s s<strong>in</strong>g<strong>in</strong>g does not generate this different responsiveness (unless the voice<br />
pitch is artificially heightened; O'Neill, Tra<strong>in</strong>or, & Trehub, 2001). Infant-directed<br />
speak<strong>in</strong>g also has a musical quality but <strong>in</strong>fants demonstrate more susta<strong>in</strong>ed attentiveness<br />
<strong>and</strong> engagement dur<strong>in</strong>g maternal s<strong>in</strong>g<strong>in</strong>g than maternal speak<strong>in</strong>g (Nakata & Trehub,<br />
2004; Trehub, 2003c).<br />
Currently, there is no widely accepted <strong>and</strong> comprehensive model how music perception<br />
develops. Initially, <strong>in</strong>fants’ resolution <strong>of</strong> frequency, tim<strong>in</strong>g, <strong>and</strong> timbre is f<strong>in</strong>er than that<br />
required for musical purposes (see Trehub, 2001 for a review). Even though, there is a<br />
grow<strong>in</strong>g body <strong>of</strong> evidence, confirm<strong>in</strong>g <strong>in</strong>fants’ disposition to structure or organize the<br />
elements <strong>of</strong> auditory patterns <strong>in</strong> a adult-like way (Trehub, 1987, 1990, 1993; Trehub &<br />
Tra<strong>in</strong>or, 1990).<br />
There are some features that are shared by most (if not all) musical cultures suggest<strong>in</strong>g<br />
<strong>in</strong>nately specified auditory mechanisms. One <strong>of</strong> these features is that most scales consist<br />
<strong>of</strong> a discrete set <strong>of</strong> five to seven pitches arranged with<strong>in</strong> the octave range (presumably<br />
result<strong>in</strong>g from constra<strong>in</strong>ts on short-term memory <strong>and</strong> categorization, cf. G. A. Miller,<br />
1956). Moreover, most scales are build <strong>of</strong> unequal <strong>in</strong>tervals lead<strong>in</strong>g to a unique set <strong>of</strong><br />
<strong>in</strong>terval relations that might be encoded more easily (Balzano, 1980, 1982; Shepard,<br />
1982; Trehub, Schellenberg, & Kamenetsky, 1999). With<strong>in</strong> the scale, <strong>in</strong>tervals with<br />
simple frequency relations – such as octave <strong>and</strong> fifth – are structurally more important:<br />
[1] Infants demonstrate octave equivalence (Demany & Arm<strong>and</strong>, 1984), [2] they prefer<br />
consonance over dissonance <strong>and</strong> categorize <strong>in</strong>tervals on the basis <strong>of</strong> their consonance<br />
(Schellenberg & Tra<strong>in</strong>or, 1996; Schellenberg & Trehub, 1996; Tra<strong>in</strong>or & He<strong>in</strong>miller,<br />
1998; Tra<strong>in</strong>or, Tsang, & Cheung, 2002; Zentner & Kagan, 1998), <strong>and</strong> [3] they more<br />
easily detect changes <strong>in</strong> sequential <strong>in</strong>tervals from simple (consonant <strong>in</strong>tervals) to complex<br />
frequency ratios (dissonant <strong>in</strong>tervals) than vice versa (Tra<strong>in</strong>or, 1997).<br />
Infants show a strong preference to rely merely on the relationships between pitches<br />
than on their absolute values. 2 Use <strong>of</strong> reference pulses <strong>and</strong> the <strong>in</strong>duction <strong>of</strong> rhythmic<br />
patterns by the asymmetrical subdivision <strong>of</strong> time pulses are also evident crossculturally.<br />
The preference for relational process<strong>in</strong>g is assumed to be restricted to human<br />
listeners (McDermott & Hauser, 2005). Relational process<strong>in</strong>g operates for pitch structure,<br />
spectral structure, <strong>and</strong> temporal structure (Hulse, Takeuchi, & Braaten, 1992) <strong>and</strong><br />
2<br />
There is some debate about how far <strong>in</strong>fants make use <strong>of</strong> absolute pitch <strong>in</strong>formation (Saffran, 2003).<br />
However, contrast<strong>in</strong>g evidence by Trehub (2003a), <strong>and</strong> Trehub, Bull <strong>and</strong> Thorpe (1984) <strong>in</strong>dicated that the<br />
use <strong>of</strong> absolute pitch <strong>in</strong>formation might merely rely on short-term memory. Plant<strong>in</strong>ga <strong>and</strong> Tra<strong>in</strong>or (2003,<br />
2005) also demonstrated a consistent priority for relative pitch process<strong>in</strong>g. Recently, Saffran, Reeck, Niebuhr,<br />
<strong>and</strong> Wilson (2005) found that <strong>in</strong>fants used relative pitch cues <strong>in</strong> task dependent manner, i.e., if such<br />
cues were more easily accessible or if absolute pitch cues were un<strong>in</strong>formative.