Structure. Heschl's gyri are one to two transverse convolutions lying on the superior temporal plane's upper surface, buried inside the lateral fissure, running mediodiaterally from the temporal lobe's insular edge; they carry the primary auditory cortex (areas 41/42 core-and-belt).
Function. Primary auditory cortex: tonotopic frequency maps (low-to-high along the gyrus), the first cortical stage of pitch, timbre and sound-source segregation. Right-hemisphere Heschl's is relatively larger for spectral resolution; damage gives cortical deafness only when bilateral.
| Instrument | Role | Tier | Credibility | Via | Observed effect |
|---|---|---|---|---|---|
| picture-naming | assessor | secondary | standard-scientific | fMRI | Heschl-plane neighbors co-activate in auditory-phonological output monitoring. |
| rhyming-judgment ↗ | assessor | secondary | standard-scientific | fMRI | Phonological code access reads at the auditory-language cortex. |
| word-listening | stimulator | primary | highly-credible | delivery | Passive speech perception drives the transverse temporal plane — the auditory-language cortex of record. |
| pitch-discrimination | stimulator | primary | highly-credible | delivery | Pitch processing drives Heschl's gyri and the transverse plane — the auditory cortex of record. |
| stream-segregation | assessor | secondary | standard-scientific | fMRI | Primary-plane engagement in stream formation. |
| phoneme-discrimination | assessor | secondary | standard-scientific | fMRI | Primary-plane reads under phonetic contrast. |
| melody-deviant | stimulator | primary | standard-scientific | delivery | The mismatch negativity generator: deviant tones drive superior temporal response automatically. |
| sound-localization | assessor | secondary | standard-scientific | fMRI | Spatial-stream processing reads at the transverse plane. |
| forward-masking | inhibitor | secondary | standard-scientific | delivery | Forward masking SUPPRESSES auditory-cortex response to the masked tone — the canonical auditory suppressive ph |
| verb-generation | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| verb-generation | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| semantic-decision ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| semantic-decision ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| picture-naming | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| lexical-decision ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| lexical-decision ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| phonemic-fluency | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| phonemic-fluency | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| sentence-comprehension | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| sentence-comprehension | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| rhyming-judgment ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| word-listening | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| repetition-priming ↗ | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| repetition-priming ↗ | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Language system of record: the paradigm engages this system (its core members are grade |
| pitch-discrimination | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| stream-segregation | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| phoneme-discrimination | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| melody-deviant | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| sound-localization | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| forward-masking | stimulator | secondary | standard-scientific | delivery | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| forward-masking | assessor | secondary | standard-scientific | fMRI | Co-engaged through the Auditory system of record: the paradigm engages this system (its core members are grade |
| repetition-priming ↗ | inhibitor | secondary | standard-scientific | delivery | Repetition suppression of the auditory-cortex response: repeated spoken words with a set pitch contour produce |
| word-listening | inhibitor | secondary | standard-scientific | delivery | Words presented repeatedly across passive and active listening blocks drove repetition suppression of BOLD in |
| oddball ↗ | inhibitor | secondary | standard-scientific | delivery | Passive syllable oddball (800 standards vs 100+100 deviants per session): MMNm source activity in left transve |
Experiences of record: Habituation studio (repetition-priming readout)
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| "Comparison of ""silent"" clustered and sparse temporal fMRI acquisitions in tonal and speech perception tasks." NeuroImage 2007 · 10.1002/hbm.20298 |
| Expectation modulates human brain responses to acute cocaine: a functional magnetic resonance imaging study. Biological psychiatry 2008 · 10.1016/j.biopsych.2007.03.021 |
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| Tit-for-tat: the neural basis of reactive aggression. NeuroImage 2007 · 10.1016/j.neuroimage.2007.07.029 |
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| Neural networks involved in voluntary and involuntary vocal pitch regulation in experienced singers. Neuropsychologia 2010 · 10.1016/j.neuropsychologia.2009.10.025 |
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| Neural substrates of phonological selection for Japanese character Kanji based on fMRI investigations. NeuroImage 2010 · 10.1016/j.neuroimage.2009.12.099 |
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| Putting the pieces together: the role of dorsolateral prefrontal cortex in relational memory encoding. Journal of cognitive neuroscience 2011 · 10.1162/jocn.2010.21459 |
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| Bidirectional connectivity between hemispheres occurs at multiple levels in language processing but depends on sex. The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.1245-10.2010 |
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| Audiovisual synchrony improves motion discrimination via enhanced connectivity between early visual and auditory areas. The Journal of neuroscience : the official journal of the Society for Neuroscience 2010 · 10.1523/JNEUROSCI.5745-09.2010 |
| Functional connectivity of the human insular cortex during noxious and innocuous thermal stimulation. NeuroImage 2011 · 10.1016/j.neuroimage.2010.09.012 |
| FMRI investigation of cross-modal interactions in beat perception: audition primes vision, but not vice versa. NeuroImage 2011 · 10.1016/j.neuroimage.2010.09.033 |
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| The neural correlates of problem states: testing FMRI predictions of a computational model of multitasking. PloS one 2010 · 10.1371/journal.pone.0012966 |
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| Eye Movements during Auditory Attention Predict Individual Differences in Dorsal Attention Network Activity. Frontiers in human neuroscience 2016 · 10.3389/fnhum.2016.00164 |
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| Sampling over Nonuniform Distributions: A Neural Efficiency Account of the Primacy Effect in Statistical Learning. Journal of cognitive neuroscience 2016 · 10.1162/jocn_a_00990 |
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| Whispering - The hidden side of auditory communication. NeuroImage 2016 · 10.1016/j.neuroimage.2016.08.023 |
| Crossmodal Processing of Haptic Inputs in Sighted and Blind Individuals. Frontiers in systems neuroscience 2016 · 10.3389/fnsys.2016.00062 |
| Effect of Mild Thyrotoxicosis on Performance and Brain Activations in a Working Memory Task. PloS one 2016 · 10.1371/journal.pone.0161552 |
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| Posterior Superior Temporal Sulcus Responses Predict Perceived Pleasantness of Skin Stroking. Frontiers in human neuroscience 2016 · 10.3389/fnhum.2016.00432 |
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| Difference in Activity in the Supplementary Motor Area Depending on Limb Combination of Hand-Foot Coordinated Movements. Frontiers in human neuroscience 2016 · 10.3389/fnhum.2016.00499 |
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| Central Pain Processing in Early-Stage Parkinson's Disease: A Laser Pain fMRI Study PMID 27776130 |
| Resting state connectivity of the human habenula at ultra-high field PMID 27780778 |
| Mentalizing in schizophrenia: A multivariate functional MRI study PMID 27793657 |
| Localization of Impaired Kinesthetic Processing Post-stroke PMID 27799902 |
| An Activation Likelihood Estimation Meta-Analysis Study of Simple Motor Movements in Older and Young Adults PMID 27799910 |
| Recruitment of Language-, Emotion- and Speech-Timing Associated Brain Regions for Expressing Emotional Prosody: Investig PMID 27803656 |
| Motor sequence learning-induced neural efficiency in functional brain connectivity PMID 27845228 |
| Prediction of Biological Motion Perception Performance from Intrinsic Brain Network Regional Efficiency PMID 27853427 |
| Empirical validation of directed functional connectivity PMID 27856312 |
| Hypoperfusion of the thalamus is associated with disability in relapsing remitting multiple sclerosis PMID 27865557 |
| Neural correlates of temporal context retrieval for abstract scrambled phrases: Reducing narrative and familiarity-based PMID 27867032 |
| Early changes in emotional processing as a marker of clinical response to SSRI treatment in depression PMID 27874847 |
| Testing the Limits of Skill Transfer for Scrabble Experts in Behavior and Brain PMID 27881960 |
| Olanzapine modulation of long- and short-range functional connectivity in the resting brain in a sample of patients with PMID 27887859 |
| Neural Basis of Working Memory Enhancement after Acute Aerobic Exercise: fMRI Study of Preadolescent Children PMID 27917141 |
| Distributed neural signatures of natural audiovisual speech and music in the human auditory cortex PMID 27932074 |
| Neural correlates of the affective properties of spontaneous and volitional laughter types PMID 27940151 |
| Brain network dysfunction in youth with obsessive-compulsive disorder induced by simple uni-manual behavior: The role of PMID 27992792 |
| Working memory circuit as a function of increasing age in healthy adolescence: A systematic review and meta-analyses PMID 27995059 |
| Automatic numerical-spatial association in synaesthesia: An fMRI investigation PMID 28025017 |
| Ipsilateral Putamen and Insula Activation by Both Left and Right GB34 Acupuncture Stimulation: An fMRI Study on Healthy PMID 28053642 |
| Resting state brain connectivity patterns before eventual relapse into cocaine abuse PMID 28057531 |
| Predicting the Multisensory Consequences of One’s Own Action: BOLD Suppression in Auditory and Visual Cortices PMID 28060861 |
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| Characterization of brain blood flow and the amplitude of low-frequency fluctuations in major depressive disorder: A mul PMID 28068619 |
| I know I’ve seen you before: Distinguishing recent-single-exposure-based familiarity from pre-existing familiarity PMID 28073651 |
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*Temporal lobe · Mai atlas of record · 1295 studies · 147 papers on disk*
Heschl's gyri are the transverse convolutions buried inside the lateral fissure on the superior temporal plane — primary auditory cortex, tonotopic frequency maps running low-to-high along the gyrus, the first cortical stage of pitch, timbre and sound-source segregation.
Heschl's gyri are one to two transverse convolutions lying on the superior temporal plane's upper surface, buried inside the lateral fissure, running mediodiaterally from the temporal lobe's insular edge; they carry the primary auditory cortex (areas 41/42 core-and-belt).
*— {'source': 'Mai, Majtanik & Paxinos', 'work': 'Atlas of the Human Brain, 4th ed., Academic Press/Elsevier', 'kind': 'atlas', 'locator': 'axial plates, MNI y −43.7…−4.2 mm, 42 plates (labels TIG/TTG)'}*
Primary auditory cortex: tonotopic frequency maps (low-to-high along the gyrus), the first cortical stage of pitch, timbre and sound-source segregation. Right-hemisphere Heschl's is relatively larger for spectral resolution; damage gives cortical deafness only when bilateral.
The functional record: primary auditory cortex — tonotopy, pitch, timbre, segregation; right-hemisphere Heschl's is specialized for pitch and musical tonality. The decoded profile is auditory through and through. The graded matrix carries the audition family: word-listening as a highly-credible stimulator, picture-naming and rhyming-judgment as standard assessors — the auditory-language seam recorded. Its coactivation map is the auditory lane's core: core+belt (2,254 shared studies — among the atlas's heaviest), superior temporal gyrus (1,281), planum temporale (1,028).
*— {'source': 'Gazzaniga, Ivry & Mangun', 'work': 'Cognitive Neuroscience: The Biology of the Mind, 4th ed., W. W. Norton', 'kind': 'textbook', 'locator': 'ch. 5, Sensation and Perception'}*
The ascending auditory hierarchy's cortical terminus — core, belt, parabelt, association, listed in shared bibliographies.
Co-activation partners of record: BA 41/42 - auditory core+belt:2254, Superior temporal gyrus:1281, Planum temporale:1028, Superior temporal sulcus:894, BA 22 - Wernicke:804, Lateral fissure:666, Cingulate gyrus, anterior:618, Supplementary motor area:539.
Cortical deafness (bilateral), the hallucination activations (Heschl's fires in auditory hallucinations), and the tonotopy's loss — the first stage's failures are hearing's cleanest cortical chapter.
10.1093/cercor/9.1.6510.1016/S0896-6273(00)80715-110.1016/S0006-3223(99)00056-610.1016/S0896-6273(00)80759-X10.1016/S0926-6410(99)00012-91295 studies total touch this region in the Neurosynth corpus of record; the full literature lives beside this dossier.
Candidate levers (Neurosynth-decoded terms — auditory(perception), speech(method-other), auditory cortex(anatomy-reference), sounds(method-other), sound(method-other), motor(action-motor), pain(interoception), sensory(method-other) …) are the foundation for the thousands of instruments to come; they are ungraded by law.
BA 41/42 - auditory core+belt:2254, Superior temporal gyrus:1281, Planum temporale:1028, Superior temporal sulcus:894 — each name is a dossier stop in this explorer.