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Re: memory for pitch
Title: Re: memory for pitch
Dear Martin et al,
Indeed - and one of the most surprising outcomes of this series
of experiments was evidence for lateral inhibition in the pitch memory
system. When you present two test tones for recognition ('same' or
'different') and these are separated by an interpolated sequence of
six tones, the error rate depends systematically on the pitch
relationship between a 'critical interpolated tone' and the first test
tone. As the interval between these two tones increases in 1/6 tone
steps, error rates increase, peak at an interval of 2/3 tone, and then
return to baseline.See
Deutsch, D. Mapping of interactions in the
pitch memory store. Science, 1972, 175,
1020-1022, posted as a PDF at
http://psy.ucsd.edu/~deutsch/psychology/deutsch_publications.htm
Furthermore, error rates increase substantially when tow tones
are interpolated, each a semitone removed from the first test
tone.See
Deutsch, D. Interference in memory between
tones adjacent in the musical scale. Journal of Experimental
Psychology, 1973, 100, 228-231.
Most persuasive is the evidence, obtained with John Feroe, of
disinhibition in pitch memory. If a tone that is 2/3 tone removed from
the first test tone (the maximally inhibiting position) is
interpolated, and a tone further removed is also interpolated, which
moves at 1/6 tone steps from the maximally inhibiting tone, you get an
orderly disinhibition function, which on modeling was found to fit a
simple Hartline-Ratliff model of a lateral inhibitory network.
See Deutsch, D. & Feroe, J.
Disinhibition in pitch memory. Perception and
Psychophysics, 1975, 17, 320-324, also posted as a PDF in the
above location.
Cheers,
Diana
Dear Diana and others,
you wrote (Monday, May 22):
...... So at least where memory for the
pitch of a
single tone is concerned, performance appears to be substantially
unrelated to rehearsal strategy, and appears to be the function of
a
low-level system that has characteristics which are very similar
to
the system that handles pitch information at the incoming
level.
Your indications of a low-level system for the short-term memory of
pitch is further supported by musical practice and by results of
research in neurophysiology.
1) In music we experience consonance and dissonance not only for
simultaneous tones, but also for non-simultaneous ones. When comparing
the two series of tones C4-F4-A4-C5 and C4-F4-A4-C#5, the first one is
perceived as more consonant than the second. Today we further assume
that this sensitivity for "horizontal harmony" is due to the
structure of the mammalian auditory brain, because also monkeys have
it (Wright et al., 2000).
In order to explain the sensory interaction of non-simultaneous tones,
some kind of internal reverberation was suggested. Clearly, if the
quality of interaction depends on acoustic frequency ratios, the
interaction must occur at a level where neural signals still contain
pitch-related periodicity information. The highest level where this
information is still present is the auditory midbrain (colliculi
inferiores).
2) Bob Zatorre and his team found in two positron emission tomographic
studies (1994, 1996) that imagination of pitch of musical tones led to
a significant activity increase also in the auditory midbrain
(colliculi inferiores).
Zatorre, R.J., Evans, A.C., Meyer, E., 1994. Neural mechanisms
underlying melodic perception and memory for pitch. J. Neurosci. 14,
1908-1919.
Zatorre, R.J., Halpern, A.R., Perry, D.W., Meyer, E., Evans, A.C.,
1996. Hearing in the mind's ear: A PET investigation of musical
imagery and perception. J. Cogn. Neurosci. 8, 29-46.
Wright, A.A., Rivera, J.J., Hulse, S.H., Shyan, M., Neiworth, J.J.,
2000. Music perception and octave generalization in rhesus monkeys. J.
Exp. Psychol. Gen. 129, 291-307.
[I wrote a short comment at:
http://web.telia.com/~u57011259/Wright.htm ]
Cheers,
Martin
----------------------------
Martin Braun
Neuroscience of Music
S-671 95 Klässbol
Sweden
web site: http://w1.570.telia.com/~u57011259/index.htm