Re: Neural mechanisms of octave equivalence ("Richard F. Lyon" )


Subject: Re: Neural mechanisms of octave equivalence
From:    "Richard F. Lyon"  <dicklyon@xxxxxxxx>
Date:    Sat, 24 Sep 2016 09:39:25 -0700
List-Archive:<http://lists.mcgill.ca/scripts/wa.exe?LIST=AUDITORY>

--001a11422caebcacbc053d4389a3 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable I agree with Alain, but looked at the paper and have a few more comments: https://www.researchgate.net/profile/Lauren_Guillette/publication/235376278= _Chickadees_fail_standardized_operant_tests_for_octave_equivalence/links/09= e4151228c5ace7d7000000.pdf Octave equivalence is pretty strong for tones with enough harmonics, for reasons that Alain describes. This paper shows that humans have some octave generalization even with pure sine waves, and that the birds do not. This likely points to different mechanisms. For matching based on common frequencies of partials, you need some partials in common, which is not the case here, due to the signals being sine waves (no upper partials). For matching based on common periods, or common peaks in autocorrelation functions, sine waves an octave apart are close, because the higher one is also periodic at the period of the lower one. So maybe this argues that humans use more period-based matching and birds use only frequency (cochlear place) matching? Maybe the experiment should be repeated with tones that have at least a second harmonic, and see if that leads to birds doing octave generalization by matching one tone's fundamental to another's second harmonic? This would be a better way to get at pitch height versus chroma, perhaps. Dick On Sat, Sep 24, 2016 at 12:59 AM, Alain de Cheveigne < alain.de.cheveigne@xxxxxxxx> wrote: > Hi Ani, > > Octave =E2=80=9Cequivalence=E2=80=9D is an emergent property of both patt= ern-matching and > autocorrelation models of pitch. All harmonics of the tone at the octave > belong to the harmonic series of the lower tone. Likewise autocorrelatio= n > peaks of the lower tone coincide with peaks of the tone at the octave. > Some neural instantiations of these models are Shihab Shamma=E2=80=99s ha= rmonic > template model, or Cariani=E2=80=99s work on autocorrelation (based on Li= cklider=E2=80=99s > ideas), and there are many others. Whether or not any specific model is > supported by anatomical or electrophysiological data is less clear. > > Actually =E2=80=9Cequivalence=E2=80=9D is a misnomer. The relation is not= commutative: the > harmonics of the lower tone do not all belong to the harmonic series of t= he > octave. Likewise peaks of the autocorrelation of the octave tone are not > all peaks of the lower tone. Thus these models would predict an asymmetr= y > in the perceptual similarity between octaves (i.e. an octave tone > =E2=80=9Cresembles=E2=80=9D the lower tone but not vice-versa). I don=E2= =80=99t know of any > relevant behavioral data or music-theoretical results on this. > > Alain > > =E2=80=94 > de Cheveign=C3=A9, A. (2005) Pitch perception models. In: Pitch - Neural = coding > and perception (Plack C, Oxenham A, eds). New York: Springer, 169-233. ( > http://audition.ens.fr/adc/pdf/2005_pitch_SHAR.pdf) > Shamma S, and Klein D (2000) The case of the missing pitch templates: how > harmonic templates emerge in the early auditory system. J Acoust Soc Am > 107:2631-2644. > Cariani PA, and Delgutte B (1996b) Neural correlates of the pitch of > complex tones. II. Pitch shift, pitch ambiguity, phase-invariance, pitch > circularity, rate-pitch and the dominance region for pitch. J Neurophysio= l > 76:1717-1734. > Licklider JCR (1951) A duplex theory of pitch perception (reproduced in > Schubert 1979, 155-160). Experientia 7:128-134. > > > > On 23 Sep 2016, at 13:06, Patel, Aniruddh D. <a.patel@xxxxxxxx> wrote: > > > > Dear List, > > > > Is anyone aware on theoretical or empirical papers on the neural > mechanisms of octave equivalence in auditory perception? > > > > Interestingly, recent works suggests that songbirds may not perceive > octave equivalence: > > > > Hoeschele, M., Weisman, R. G., Guillette, L. M., Hahn, A. H., & Sturdy, > C. B. (2013). Chickadees fail standardized operant tests for octave > equivalence. Animal cognition, 16(4), 599-609. > > > > Thanks, > > > > Ani Patel > > > > Aniruddh D. Patel > > Professor > > Dept. of Psychology > > Tufts University > > 490 Boston Ave. > > Medford, MA 02155 > > > > Senior Fellow > > Canadian Institute for Advanced Research (CIFAR) > > Azrieli Program in Brain, Mind, & Consciousness > > > > a.patel@xxxxxxxx > > http://ase.tufts.edu/psychology/people/patel/ > --001a11422caebcacbc053d4389a3 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable <div dir=3D"ltr"><div><div><div><div>I agree with Alain, but looked at the = paper and have a few more comments:<br><a href=3D"https://www.researchgate.= net/profile/Lauren_Guillette/publication/235376278_Chickadees_fail_standard= ized_operant_tests_for_octave_equivalence/links/09e4151228c5ace7d7000000.pd= f">https://www.researchgate.net/profile/Lauren_Guillette/publication/235376= 278_Chickadees_fail_standardized_operant_tests_for_octave_equivalence/links= /09e4151228c5ace7d7000000.pdf</a><br><br></div>Octave equivalence is pretty= strong for tones with enough harmonics, for reasons that Alain describes.= =C2=A0 This paper shows that humans have some octave generalization even wi= th pure sine waves, and that the birds do not.=C2=A0 This likely points to = different mechanisms.<br><br></div>For matching based on common frequencies= of partials, you need some partials in common, which is not the case here,= due to the signals being sine waves (no upper partials).=C2=A0 For matchin= g based on common periods, or common peaks in autocorrelation functions, si= ne waves an octave apart are close, because the higher one is also periodic= at the period of the lower one.<br><br></div>So maybe this argues that hum= ans use more period-based matching and birds use only frequency (cochlear p= lace) matching?=C2=A0 Maybe the experiment should be repeated with tones th= at have at least a second harmonic, and see if that leads to birds doing oc= tave generalization by matching one tone&#39;s fundamental to another&#39;s= second harmonic?=C2=A0 This would be a better way to get at pitch height v= ersus chroma, perhaps.<br><br></div>Dick<br><br></div><div class=3D"gmail_e= xtra"><br><div class=3D"gmail_quote">On Sat, Sep 24, 2016 at 12:59 AM, Alai= n de Cheveigne <span dir=3D"ltr">&lt;<a href=3D"mailto:alain.de.cheveigne@xxxxxxxx= ns.fr" target=3D"_blank">alain.de.cheveigne@xxxxxxxx</a>&gt;</span> wrote:<br= ><blockquote class=3D"gmail_quote" style=3D"margin:0 0 0 .8ex;border-left:1= px #ccc solid;padding-left:1ex">Hi Ani,<br> <br> Octave =E2=80=9Cequivalence=E2=80=9D is an emergent property of both patter= n-matching and autocorrelation models of pitch. All harmonics of the tone a= t the octave belong to the harmonic series of the lower tone.=C2=A0 Likewis= e autocorrelation peaks of the lower tone coincide with peaks of the tone a= t the octave.=C2=A0 Some neural instantiations of these models are Shihab S= hamma=E2=80=99s harmonic template model, or Cariani=E2=80=99s work on autoc= orrelation (based on Licklider=E2=80=99s ideas), and there are many others.= =C2=A0 Whether or not any specific model is supported by anatomical or elec= trophysiological data is less clear.<br> <br> Actually =E2=80=9Cequivalence=E2=80=9D is a misnomer. The relation is not c= ommutative: the harmonics of the lower tone do not all belong to the harmon= ic series of the octave.=C2=A0 Likewise peaks of the autocorrelation of the= octave tone are not all peaks of the lower tone.=C2=A0 Thus these models w= ould predict an asymmetry in the perceptual similarity between octaves (i.e= . an octave tone =E2=80=9Cresembles=E2=80=9D the lower tone but not vice-ve= rsa).=C2=A0 I don=E2=80=99t know of any relevant behavioral data or music-t= heoretical results on this.<br> <br> Alain<br> <br> =E2=80=94<br> de Cheveign=C3=A9, A. (2005) Pitch perception models. In: Pitch - Neural co= ding and perception (Plack C, Oxenham A, eds). New York: Springer, 169-233.= (<a href=3D"http://audition.ens.fr/adc/pdf/2005_pitch_SHAR.pdf" rel=3D"nor= eferrer" target=3D"_blank">http://audition.ens.fr/adc/<wbr>pdf/2005_pitch_S= HAR.pdf</a>)<br> Shamma S, and Klein D (2000) The case of the missing pitch templates: how h= armonic templates emerge in the early auditory system. J Acoust Soc Am 107:= 2631-2644.<br> Cariani PA, and Delgutte B (1996b) Neural correlates of the pitch of comple= x tones. II. Pitch shift, pitch ambiguity, phase-invariance, pitch circular= ity, rate-pitch and the dominance region for pitch. J Neurophysiol 76:1717-= 1734.<br> Licklider JCR (1951) A duplex theory of pitch perception (reproduced in Sch= ubert 1979, 155-160). Experientia 7:128-134.<br> <div class=3D"HOEnZb"><div class=3D"h5"><br> <br> &gt; On 23 Sep 2016, at 13:06, Patel, Aniruddh D. &lt;<a href=3D"mailto:a.p= atel@xxxxxxxx">a.patel@xxxxxxxx</a>&gt; wrote:<br> &gt;<br> &gt; Dear List,<br> &gt;<br> &gt; Is anyone aware on theoretical or empirical papers on the neural mecha= nisms of octave equivalence in auditory perception?<br> &gt;<br> &gt; Interestingly, recent works suggests that songbirds may not perceive o= ctave equivalence:<br> &gt;<br> &gt; Hoeschele, M., Weisman, R. G., Guillette, L. M., Hahn, A. H., &amp; St= urdy, C. B. (2013). Chickadees fail standardized operant tests for octave e= quivalence. Animal cognition, 16(4), 599-609.<br> &gt;<br> &gt; Thanks,<br> &gt;<br> &gt; Ani Patel<br> &gt;<br> &gt; Aniruddh D. Patel<br> &gt; Professor<br> &gt; Dept. of Psychology<br> &gt; Tufts University<br> &gt; 490 Boston Ave.<br> &gt; Medford, MA 02155<br> &gt;<br> &gt; Senior Fellow<br> &gt; Canadian Institute for Advanced Research (CIFAR)<br> &gt; Azrieli Program in Brain, Mind, &amp; Consciousness<br> &gt;<br> &gt; <a href=3D"mailto:a.patel@xxxxxxxx">a.patel@xxxxxxxx</a><br> &gt; <a href=3D"http://ase.tufts.edu/psychology/people/patel/" rel=3D"noref= errer" target=3D"_blank">http://ase.tufts.edu/<wbr>psychology/people/patel/= </a><br> </div></div></blockquote></div><br></div> --001a11422caebcacbc053d4389a3--


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