SlideShare a Scribd company logo
3. Natural speech
2. Methods
1. Introduc�on
Inves�ga�ng the neural code for speech discrimina�on
MRC Ins�tute of Hearing Research, No�ngham, UK
mark.steadman@ihr.mrc.ac.uk
Mark Steadman & Chris Sumner
4. Vocoded speech
5. Summary
Speech recogni�on is robust to severe degrada�ons e.g. cochlear
impants, vocoded speech.
Human psychophysical studies using degraded speech sounds cons�tute
a powerful toolset to explore the neural bases of speech percep�on.
Inves�ga�ng which aspects of the neural representa�on facilitate robust
speech discrimina�on, and how this changes throughout the auditory
brain, increases our understanding of neural processing of complex
signals.
Medial consonants elicit dis�nct pa�erns of ac�vity in the auditory nerve, inferior
colliculus and auditory cortex of anaesthe�sed guinea pigs.
The efficacy of spike �ming depends on the nature of the task (speech token vs.
consonant recogni�on) and the brain region.
Unlike percep�on, discriminability of peripheral representa�ons is highly robust to
severe spectral degrada�ons in the s�mulus, provided temporal cues are preserved.
Cor�cal representa�ons of speech sounds are less redundant for a speech
discrimina�on task than those in the more peripheral nuclei.
Shannon, Robert V., et al. "Speech recogni�on with primarily temporal cues." Science 270.5234 (1995): 303-304.
References:
Computa�onal model (auditory nerve)
Outer/middle
ear filter
Nonlinear basilar
membrane filterbank
Inner hair cell
transduc�on model
Stochas�c spike
genera�on
Neural classifica�on
Neural
Classifier
% Correct
�me since onset, ms
neuron#
300 400 500
/asa/ neurogram
(auditory nerve)
Auditory Nerve Auditory CortexInferior Colliculus
200 300 400 200 300 400200 300 400
/ada/
200 300 400 200 300 400200 300 400
/asa/
200 300 400 200 300 400200 300 400
/ama/
Figure: Example neurograms from each brain region for 4 of the 16 consonants.
1 10 100100 101 102
0
20
40
60
80
100
100 101 102
percentcorrect
one talker three talkers
Auditory nerve Inferior colliculus Auditory cortex
smoothing window length, ms number of recording sites
chance
100 sites 106 sites 196 sites
Figure: Discriminability of representa�ons of vocoded speech with op�mal smoothing. Human psychophysics
taken from Shannon et al. (1995).
Electrophysiology
Inferior colliculus
Auditory cortex
in vivo extracellular recordings in the inferior
colliculus and auditory cortex of anaesthe�sed
guinea pigs.
S�mulus set parametrically degraded using a noise vocoder using 1, 2, 4 and 8
spectral channels (between 0.1 and 4 kHz), with 16 and 500 Hz envelope rates.
S�muli
16 a-consonant-a sequences.
3 male talkers.
Parametrically degraded using a "noise vocoder".
Bandpass
filter
Envelope
extraction
Noise
Bandpass
filter
0 100 200 300 400 500 600
0
1
2
3
4
original s�mulus
�me, ms
frequency,kHz
0 100 200 300 400 500 600
0
1
2
3
4
vocoded s�mulus
�me, ms
frequency,kHz
Mul�-unit spiking ac�vity extracted by
filtering and thresholding raw signal.
Nearest-neighbour based classifier trained on
average "neurograms".
Average neurograms were (op�onally) combined
across talkers.
Neurograms are allowed to temporally shi�
rela�ve to each other such that distances were
minimised.
Neurograms were parametrically smoothed by row-wise convolu�on
prior to classifier training and tes�ng.
For a single talker speech token discrimina�on task, representa�ons in the auditory
nerve and IC are prefectly discriminable regardless of smoothing window length.
Unlike data from an analogous human psychophyics task, high rate envelope cues
increase the discriminability of neural responses In the auditory nerve and IC This is
not the case in the auditory cortex.
This benefit is only apparent where millisecond-precise spike �ming is considered in
the auditory nerve, but is s�ll apparent in the IC where longer smoothing windows
are used.
Cor�cal representa�ons are perfectly discriminable with op�mal smoothing windows.
Where the classifier was trained using representa�ons combined across talkers,
discriminabilty is highly depended on choice of smoothing window.
For a comparable number of neurons, representa�ons are far more discriminable in
the auditory nerve and inferior colliculus than in the cortex.
Decreasing the spectral complexity of the signal has less effect on the discriminability
of peripheral representa�ons than it has on percep�on.

More Related Content

Viewers also liked

Etnicheski malcinstva ef
Etnicheski malcinstva efEtnicheski malcinstva ef
Etnicheski malcinstva ef
Albena Popova
 
12.08 clo axonify_final
12.08 clo axonify_final12.08 clo axonify_final
12.08 clo axonify_final
Human Capital Media
 
latissa philliprs resume 15
latissa philliprs resume 15latissa philliprs resume 15
latissa philliprs resume 15
Latissa Phillips
 
about.infinit.brochure.9.2014
about.infinit.brochure.9.2014about.infinit.brochure.9.2014
about.infinit.brochure.9.2014
Jerod Powell
 
Mi apa
Mi apaMi apa
Sebastian cabrera l
Sebastian cabrera lSebastian cabrera l
Sebastian cabrera l
eshluhe
 
CV Talha
CV TalhaCV Talha
CV Talha
Talha Bin Naeem
 
Ejemplos de factorizacion
Ejemplos de factorizacionEjemplos de factorizacion
Ejemplos de factorizacionFabian Muñoz
 
Task 3
Task 3Task 3
Task 3
shannoncloee
 
Lamk kampuskatsaus LPR 03122013
Lamk kampuskatsaus LPR 03122013Lamk kampuskatsaus LPR 03122013
Lamk kampuskatsaus LPR 03122013Outi Kallioinen
 

Viewers also liked (10)

Etnicheski malcinstva ef
Etnicheski malcinstva efEtnicheski malcinstva ef
Etnicheski malcinstva ef
 
12.08 clo axonify_final
12.08 clo axonify_final12.08 clo axonify_final
12.08 clo axonify_final
 
latissa philliprs resume 15
latissa philliprs resume 15latissa philliprs resume 15
latissa philliprs resume 15
 
about.infinit.brochure.9.2014
about.infinit.brochure.9.2014about.infinit.brochure.9.2014
about.infinit.brochure.9.2014
 
Mi apa
Mi apaMi apa
Mi apa
 
Sebastian cabrera l
Sebastian cabrera lSebastian cabrera l
Sebastian cabrera l
 
CV Talha
CV TalhaCV Talha
CV Talha
 
Ejemplos de factorizacion
Ejemplos de factorizacionEjemplos de factorizacion
Ejemplos de factorizacion
 
Task 3
Task 3Task 3
Task 3
 
Lamk kampuskatsaus LPR 03122013
Lamk kampuskatsaus LPR 03122013Lamk kampuskatsaus LPR 03122013
Lamk kampuskatsaus LPR 03122013
 

Similar to poster

Physiology of Acoustic & Vestibular analyzer
Physiology of Acoustic & Vestibular analyzer Physiology of Acoustic & Vestibular analyzer
Physiology of Acoustic & Vestibular analyzer
Eneutron
 
Response Properties of Single Auditory Nerve Fibers in the Mouse
Response Properties of Single Auditory Nerve Fibers in the MouseResponse Properties of Single Auditory Nerve Fibers in the Mouse
Response Properties of Single Auditory Nerve Fibers in the Mouse
Annette Taberner-Miller, Ph.D.
 
SPEECH PERCEPTION MASLP
SPEECH PERCEPTION MASLPSPEECH PERCEPTION MASLP
SPEECH PERCEPTION MASLP
HimaniBansal15
 
Echolocation in Bats
Echolocation in BatsEcholocation in Bats
Echolocation in Bats
Krishnendu Sinha
 
Thesis_revised200216 (4)
Thesis_revised200216 (4)Thesis_revised200216 (4)
Thesis_revised200216 (4)
Itai Hershenhoren
 
Chambers, Salazar, Polley
Chambers, Salazar, PolleyChambers, Salazar, Polley
Chambers, Salazar, Polley
Juan Jose Salazar
 
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza SyedBAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
Murtaza Syed
 
Facial nerve and disorder
Facial nerve and disorderFacial nerve and disorder
Facial nerve and disorder
Gurchand Behal
 
Sensory systems 3
Sensory systems 3Sensory systems 3
Sensory systems 3
whisper119
 
Auditory pathways
Auditory pathwaysAuditory pathways
Auditory pathways
“Karishma R.Pandey”
 
Coincidence analysis of the effect of cochlear disparities on temporal respo...
Coincidence analysis of the effect of cochlear  disparities on temporal respo...Coincidence analysis of the effect of cochlear  disparities on temporal respo...
Coincidence analysis of the effect of cochlear disparities on temporal respo...
TeruKamogashira
 
deafness ppt.pptx
deafness ppt.pptxdeafness ppt.pptx
deafness ppt.pptx
Reena Gollapalli
 
Manuscript
ManuscriptManuscript
Manuscript
Steven Elias King
 
3. speech processing algorithms for perception improvement of hearing impaire...
3. speech processing algorithms for perception improvement of hearing impaire...3. speech processing algorithms for perception improvement of hearing impaire...
3. speech processing algorithms for perception improvement of hearing impaire...
k srikanth
 
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
HEARnet _
 
Sensorimotor interplay in vocal communication
Sensorimotor interplay in vocal communicationSensorimotor interplay in vocal communication
Sensorimotor interplay in vocal communication
Satadru Dey
 
Music and the brain
Music and the brainMusic and the brain
Music and the brain
MedicineAndHealthNeurolog
 
NOISE INDUCED HEARING LOSS
NOISE INDUCED HEARING LOSSNOISE INDUCED HEARING LOSS
NOISE INDUCED HEARING LOSS
Dr.Kaushik Sutradhar
 
Clinical neuroanatomy of vestibulocochlear nerve
Clinical neuroanatomy of vestibulocochlear nerveClinical neuroanatomy of vestibulocochlear nerve
Clinical neuroanatomy of vestibulocochlear nerve
ChirayuRegmi2
 
BERA AND otoacoustic emission edited.pptx
BERA AND  otoacoustic emission edited.pptxBERA AND  otoacoustic emission edited.pptx
BERA AND otoacoustic emission edited.pptx
Manu Babu
 

Similar to poster (20)

Physiology of Acoustic & Vestibular analyzer
Physiology of Acoustic & Vestibular analyzer Physiology of Acoustic & Vestibular analyzer
Physiology of Acoustic & Vestibular analyzer
 
Response Properties of Single Auditory Nerve Fibers in the Mouse
Response Properties of Single Auditory Nerve Fibers in the MouseResponse Properties of Single Auditory Nerve Fibers in the Mouse
Response Properties of Single Auditory Nerve Fibers in the Mouse
 
SPEECH PERCEPTION MASLP
SPEECH PERCEPTION MASLPSPEECH PERCEPTION MASLP
SPEECH PERCEPTION MASLP
 
Echolocation in Bats
Echolocation in BatsEcholocation in Bats
Echolocation in Bats
 
Thesis_revised200216 (4)
Thesis_revised200216 (4)Thesis_revised200216 (4)
Thesis_revised200216 (4)
 
Chambers, Salazar, Polley
Chambers, Salazar, PolleyChambers, Salazar, Polley
Chambers, Salazar, Polley
 
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza SyedBAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
BAEP, BERA, BEP, Brainstem auditory evoked potential By Murtaza Syed
 
Facial nerve and disorder
Facial nerve and disorderFacial nerve and disorder
Facial nerve and disorder
 
Sensory systems 3
Sensory systems 3Sensory systems 3
Sensory systems 3
 
Auditory pathways
Auditory pathwaysAuditory pathways
Auditory pathways
 
Coincidence analysis of the effect of cochlear disparities on temporal respo...
Coincidence analysis of the effect of cochlear  disparities on temporal respo...Coincidence analysis of the effect of cochlear  disparities on temporal respo...
Coincidence analysis of the effect of cochlear disparities on temporal respo...
 
deafness ppt.pptx
deafness ppt.pptxdeafness ppt.pptx
deafness ppt.pptx
 
Manuscript
ManuscriptManuscript
Manuscript
 
3. speech processing algorithms for perception improvement of hearing impaire...
3. speech processing algorithms for perception improvement of hearing impaire...3. speech processing algorithms for perception improvement of hearing impaire...
3. speech processing algorithms for perception improvement of hearing impaire...
 
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
MEG system for cochlear implants ecipients and auditory entrainment - HEARing...
 
Sensorimotor interplay in vocal communication
Sensorimotor interplay in vocal communicationSensorimotor interplay in vocal communication
Sensorimotor interplay in vocal communication
 
Music and the brain
Music and the brainMusic and the brain
Music and the brain
 
NOISE INDUCED HEARING LOSS
NOISE INDUCED HEARING LOSSNOISE INDUCED HEARING LOSS
NOISE INDUCED HEARING LOSS
 
Clinical neuroanatomy of vestibulocochlear nerve
Clinical neuroanatomy of vestibulocochlear nerveClinical neuroanatomy of vestibulocochlear nerve
Clinical neuroanatomy of vestibulocochlear nerve
 
BERA AND otoacoustic emission edited.pptx
BERA AND  otoacoustic emission edited.pptxBERA AND  otoacoustic emission edited.pptx
BERA AND otoacoustic emission edited.pptx
 

poster

  • 1. 3. Natural speech 2. Methods 1. Introduc�on Inves�ga�ng the neural code for speech discrimina�on MRC Ins�tute of Hearing Research, No�ngham, UK mark.steadman@ihr.mrc.ac.uk Mark Steadman & Chris Sumner 4. Vocoded speech 5. Summary Speech recogni�on is robust to severe degrada�ons e.g. cochlear impants, vocoded speech. Human psychophysical studies using degraded speech sounds cons�tute a powerful toolset to explore the neural bases of speech percep�on. Inves�ga�ng which aspects of the neural representa�on facilitate robust speech discrimina�on, and how this changes throughout the auditory brain, increases our understanding of neural processing of complex signals. Medial consonants elicit dis�nct pa�erns of ac�vity in the auditory nerve, inferior colliculus and auditory cortex of anaesthe�sed guinea pigs. The efficacy of spike �ming depends on the nature of the task (speech token vs. consonant recogni�on) and the brain region. Unlike percep�on, discriminability of peripheral representa�ons is highly robust to severe spectral degrada�ons in the s�mulus, provided temporal cues are preserved. Cor�cal representa�ons of speech sounds are less redundant for a speech discrimina�on task than those in the more peripheral nuclei. Shannon, Robert V., et al. "Speech recogni�on with primarily temporal cues." Science 270.5234 (1995): 303-304. References: Computa�onal model (auditory nerve) Outer/middle ear filter Nonlinear basilar membrane filterbank Inner hair cell transduc�on model Stochas�c spike genera�on Neural classifica�on Neural Classifier % Correct �me since onset, ms neuron# 300 400 500 /asa/ neurogram (auditory nerve) Auditory Nerve Auditory CortexInferior Colliculus 200 300 400 200 300 400200 300 400 /ada/ 200 300 400 200 300 400200 300 400 /asa/ 200 300 400 200 300 400200 300 400 /ama/ Figure: Example neurograms from each brain region for 4 of the 16 consonants. 1 10 100100 101 102 0 20 40 60 80 100 100 101 102 percentcorrect one talker three talkers Auditory nerve Inferior colliculus Auditory cortex smoothing window length, ms number of recording sites chance 100 sites 106 sites 196 sites Figure: Discriminability of representa�ons of vocoded speech with op�mal smoothing. Human psychophysics taken from Shannon et al. (1995). Electrophysiology Inferior colliculus Auditory cortex in vivo extracellular recordings in the inferior colliculus and auditory cortex of anaesthe�sed guinea pigs. S�mulus set parametrically degraded using a noise vocoder using 1, 2, 4 and 8 spectral channels (between 0.1 and 4 kHz), with 16 and 500 Hz envelope rates. S�muli 16 a-consonant-a sequences. 3 male talkers. Parametrically degraded using a "noise vocoder". Bandpass filter Envelope extraction Noise Bandpass filter 0 100 200 300 400 500 600 0 1 2 3 4 original s�mulus �me, ms frequency,kHz 0 100 200 300 400 500 600 0 1 2 3 4 vocoded s�mulus �me, ms frequency,kHz Mul�-unit spiking ac�vity extracted by filtering and thresholding raw signal. Nearest-neighbour based classifier trained on average "neurograms". Average neurograms were (op�onally) combined across talkers. Neurograms are allowed to temporally shi� rela�ve to each other such that distances were minimised. Neurograms were parametrically smoothed by row-wise convolu�on prior to classifier training and tes�ng. For a single talker speech token discrimina�on task, representa�ons in the auditory nerve and IC are prefectly discriminable regardless of smoothing window length. Unlike data from an analogous human psychophyics task, high rate envelope cues increase the discriminability of neural responses In the auditory nerve and IC This is not the case in the auditory cortex. This benefit is only apparent where millisecond-precise spike �ming is considered in the auditory nerve, but is s�ll apparent in the IC where longer smoothing windows are used. Cor�cal representa�ons are perfectly discriminable with op�mal smoothing windows. Where the classifier was trained using representa�ons combined across talkers, discriminabilty is highly depended on choice of smoothing window. For a comparable number of neurons, representa�ons are far more discriminable in the auditory nerve and inferior colliculus than in the cortex. Decreasing the spectral complexity of the signal has less effect on the discriminability of peripheral representa�ons than it has on percep�on.