Professor Dr.-Ing. Hugo Fastl, Professor Dr.-Ing. Eberhard — Psychoacoustics- Facts and Models

Yield

659 of 3380 paragraphs kept (19.5%). Target for mining: 30%–50% — ⚠️ BELOW target.

Pre-Assessment

This is a well-established, standard academic reference text in psychoacoustics. Hugo Fastl was a professor at the Technical University of Munich and a leading figure in auditory perception research, co-authoring this work with Eberhard Zwicker, who essentially founded the German school of psychoacoustics with his classic models of loudness, masking, and critical bands. As a “Facts and Models” title, it is deliberately structured to deliver precisely what the reading stance promises: empirical data alongside the quantitative models (loudness, fluctuation strength, sharpness, roughness, masking) that organize those facts. The edition matters for currency — the Zwicker models are decades old and largely settled science; newer editions incorporate Fastl’s later work but the field’s core models haven’t radically shifted. Expected yield is heavily weighted toward concepts/frameworks (the models and their derivations) backed by a solid factual/empirical base, with almost none of the inspirational or speculative register. For a mining read, this is an ideal source: dense, systematic, and authoritative, though notation-heavy and best read with general linear algebra and signal-processing fundamentals in hand. I can’t verify which edition you hold without more detail, but the authority of the authors and the purpose-fit of the text are unambiguous.

Reading Goal

Prioritizing: Factual Claims (Reader wants facts about psychoacoustics, so empirical findings are central.), Definitional Content (Understanding concepts requires clear definitions of key terms and models.), Causal Relationships (Models often explain cause-and-effect between physical stimuli and perception.), Contrarian or Surprising Claims (Counterintuitive perceptual phenomena are part of mastering the subject.), Connection Points (Tying psychoacoustics to neuroscience and physics aids model understanding.) De-prioritizing: Craft and Method (Method is secondary to comprehension-focused reading.), Inspiration and Speculation (Reader seeks established knowledge, not speculative extrapolation.)

Thesis

Human hearing spans sound pressures from 10-5 to 102 Pa · ch. 0

Argument

  1. White noise shows frequency-flat long-term spectra but frequency-dependent short-term spectra — ch. 0
  2. An amplitude-modulated tone is a carrier plus two side lines — ch. 0
  3. Gaussian-shaped tone bursts minimize spectral splatter in gated tones — ch. 0
  4. A single tone burst yields a continuous spectrum while periodic pulses yield line spectra — ch. 0
  5. Noise envelope fluctuation rate is inversely proportional to bandwidth — ch. 0
  6. Periodic gating creates spectral line spacings set by the pulse repetition rate — ch. 0
  7. Psychoacoustics is the quantitative science of the ear as an information receiver. — ch. 0
  8. Filter bandwidth limits how fast a band-pass noise envelope can fluctuate — ch. 0
  9. Gaussian shapes minimize the bandwidth-duration product — ch. 0
  10. Psychoacoustic phenomena can be experienced directly through audio demonstrations. — ch. 0
  11. Median and interquartile range stay scale-invariant where means fail — ch. 1
  12. Active stimulus control by subjects can bias psychophysical measurements — ch. 1
  13. Switching a tone on and off generates broadband transient clicks in distant frequency bands — ch. 1
  14. Outer haircells act locally within the cochlea to modulate inner haircells — ch. 1
  15. Outer haircells amplify quiet sounds only, while inner haircells respond directly to loud ones. — ch. 1
  16. Human hearing spans 150 dB and three decades of frequency — ch. 1
  17. The four otoacoustic emission types are distinguished by whether and how they are evoked — ch. 1
  18. Physical stimuli map to separate hearing sensations only within audible physical ranges — ch. 1
  19. Forced-choice procedures inform subjects after each trial which interval held the signal. — ch. 1
  20. Abrupt tone onset and offset generate broadband transient energy at distant frequencies. — ch. 1
  21. Hearing is most damage-prone in the 3-8 kHz frequency range — ch. 1
  22. Normal hearing is most sensitive near 2 to 5 kHz — ch. 1
  23. Transforming a stimulus scale shifts where means but not medians fall — ch. 1
  24. The inner ear acts as a linear system offering both frequency and temporal resolution. — ch. 1
  25. The inner ear amplifies quiet sounds by up to 30 dB through active feedback. — ch. 1
  26. Tracking methods differ from adjustment by letting subjects control only direction, not magnitude — ch. 1
  27. Psychoacoustic tuning curves directly reflect cochlear mechanical processing. — ch. 1
  28. Young headphone users already show measurable hearing damage in the 3-12 kHz range — ch. 1
  29. Halving exposure duration permits a 10 dB increase in safe sound level — ch. 1
  30. A low-level-only dip in tuning curves reveals the ear’s active frequency-enhancing processes — ch. 1
  31. The threshold in quiet is highly reproducible for individual subjects — ch. 1
  32. Psychoacoustic results depend on experimental procedure and sensitivity rises with alternatives. — ch. 1
  33. Psychoacoustic headphones distort sound unless free-field equalized to compensate their band-pass response — ch. 1
  34. The cochlea can be modeled as a bank of overlapping asymmetric bandpass filters — ch. 1
  35. Hearing damage risk halves allowed exposure time for every roughly 10 dB increase — ch. 1
  36. The ear is most easily damaged between 3 and 8 kHz — ch. 1
  37. The median resists stimulus-scale transformations, unlike arithmetic and geometric means — ch. 1
  38. Music occupies a wider frequency and dynamic range than speech — ch. 1
  39. Hearing sensations correlate with stimulus magnitudes but only within the audible range — ch. 1
  40. Feedback in outer haircells enhances sensitivity while lateral spread shapes frequency selectivity. — ch. 1
  41. Cochlear amplification is instantaneous and symmetrically saturating in its transfer. — ch. 1
  42. Magnitude estimation lets listeners assign numbers proportional to perceived loudness. — ch. 1
  43. Repeated noise overexposure converts temporary threshold shifts into permanent hearing loss — ch. 1
  44. The inner ear can be modeled as an array of asymmetrical overlapping bandpass filters. — ch. 1
  45. Threshold in quiet is individually reproducible to within plus or minus six decibels — ch. 1
  46. Spontaneous otoacoustic emissions show a minimum frequency spacing that grows with frequency — ch. 1
  47. The choice of averaging unit among level, pressure, or intensity critically shapes threshold data. — ch. 1
  48. Inner hair cells form one row while outer hair cells form three rows — ch. 1
  49. Absolute hearing threshold is a statistical construct, defined at 50% detection probability. — ch. 1
  50. Inner and outer hair cells differ structurally and likely function differently — ch. 1
  51. Auditory tuning curves derive from constant basilar membrane velocity rather than displacement — ch. 1
  52. Outer hair cells actively amplify and sharpen sound before inner hair cells fire — ch. 1
  53. Yes-No procedures force signal detection decisions without an unsure option — ch. 1
  54. Bekesy-tracking measures threshold curves by letting the subject reverse intensity direction — ch. 1
  55. Adaptive procedures adjust stimulus intensity based on prior responses and converge on thresholds — ch. 1
  56. Basilar membrane displacements during speech are only tens of nanometers, near atomic scale — ch. 1
  57. Spontaneous emission frequencies remain stable to within one percent — ch. 2
  58. Present spontaneous emissions indicate good hearing, absent ones prove nothing — ch. 2
  59. Suppressor tones reveal tuning curves matching neural frequency selectivity — ch. 2
  60. SOAE levels fluctuate widely while their frequencies stay remarkably stable — ch. 2
  61. Suppressor tones that reduce SOAEs map the ear’s fine frequency selectivity — ch. 2
  62. Delayed evoked emissions are the ear’s response to short impulses — ch. 3
  63. Spontaneous and evoked otoacoustic emissions likely share a single source — ch. 3
  64. Delayed evoked emissions respond linearly to impulses below about 18 dB sensation level — ch. 3
  65. Most human ears display synchronized spontaneous otoacoustic emissions when driven — ch. 3
  66. Delayed otoacoustic emissions grow linearly then saturate 10-20 dB above threshold — ch. 4
  67. Delayed otoacoustic emissions obey linear superposition at low amplitudes — ch. 4
  68. Suppression of evoked emissions tracks the audibility of the evoking tone — ch. 5
  69. Delayed evoked otoacoustic emissions show discrete spectral peaks rather than continuous energy — ch. 5
  70. Delayed otoacoustic emissions arrive faster for higher stimulus frequencies — ch. 5
  71. Inner hair cells only convert oscillations to spike rates in the model — ch. 6
  72. Masking disrupts everyday speech and music whenever competing sounds differ in level — ch. 6
  73. Uniform masking noise mirrors white-noise masking and gives flat thresholds — ch. 6
  74. Density level converts to total level once bandwidth is known — ch. 6
  75. Simultaneous masking raises a test tone’s just-audible level above threshold in quiet. — ch. 6
  76. Outer and middle ear act linearly while inner-ear mechanics are nonlinear — ch. 6
  77. Critical bandwidth stays constant near 100 Hz up to 500 Hz then grows — ch. 6
  78. Spacing of hearing-threshold minima matches the 180-degree phase-shift frequency distance — ch. 6
  79. Otoacoustic emission suppression mirrors hearing threshold masking patterns — ch. 6
  80. Masking can occur even when the masker follows the test sound in time. — ch. 6
  81. Masking pattern shapes differ by center frequency even at equal masker level — ch. 6
  82. Spontaneous otoacoustic emissions align with peaks in stimulus-frequency fine structure — ch. 6
  83. Masked threshold always exceeds quiet threshold except when masker and test frequencies differ greatly — ch. 6
  84. Outer hair cells act as nonlinear amplifiers with bidirectional lateral feedback — ch. 6
  85. Low-frequency suppressor impulses suppress cochlear emissions most at rarefaction peaks — ch. 6
  86. Basilar-membrane models are validated by frequency responses comparable to tuning curves — ch. 6
  87. Threshold in quiet has a fine structure of maxima and minima. — ch. 6
  88. Masking is graded, with partial masking reducing loudness rather than audibility. — ch. 6
  89. Analog hearing models let experimenters measure physical states real ears hide — ch. 6
  90. A single source generates all three kinds of otoacoustic emissions. — ch. 6
  91. Low-frequency suppressors reduce emissions by saturating cochlear feedback-loop nonlinearity — ch. 6
  92. Distortion product emissions are objectively measurable in the ear canal — ch. 6
  93. Frequency-ripple spacing and emission delay time are inversely related — ch. 6
  94. Forward masking follows masker termination and is also called post masking — ch. 6
  95. Two tones presented together produce audible combination tones in the ear — ch. 6
  96. White noise masking of tones is linear but frequency-dependent above 500 Hz — ch. 6
  97. Individual auditory fibres cover only 40-60 dB yet we hear over 100 dB range — ch. 6
  98. Broad-band noise masking erases individual differences in quiet threshold — ch. 6
  99. Delayed otoacoustic emissions arise from decaying basilar-membrane oscillations that sum in phase — ch. 6
  100. Basilar-membrane resonance peaks shift downward as input level rises — ch. 6
  101. Combination tones can be cancelled by adding matched opposite-phase tones — ch. 6
  102. Distortion product emissions arise only in a live ear, not passive cavities — ch. 6
  103. Masking measurements require noise slopes steeper than the ear’s own selectivity — ch. 6
  104. Equal-level narrow-band maskers mask less at higher centre frequencies — ch. 6
  105. Combination tones arise from the hearing system’s own nonlinearity — ch. 7
  106. Masked threshold rise toward high frequencies is about 100 dB per octave. — ch. 7
  107. Instrument timbre differences stem from harmonic spectra that shape masking breadth — ch. 7
  108. Tonal maskers create distinct audible regions beyond simple masking — ch. 7
  109. Odd-order difference tones explain why single tones mask differently than noise — ch. 7
  110. Five tones replicate narrow-band noise masking while single tones distort it — ch. 7
  111. Masking by bandlimited noise depends only on masker energy within the critical band. — ch. 7
  112. Masking pattern curves are scale-invariant and predictable by horizontal shifts — ch. 7
  113. The near-miss of Weber’s law means threshold slopes can reach 3 to 6 — ch. 7
  114. Tonal masker spread inverts from low to high frequencies as masker level rises — ch. 7
  115. Harmonic spacing on a log scale determines masking-pattern dip size — ch. 7
  116. The masked threshold’s high-frequency slope steepness depends on masker level — ch. 7
  117. Postmasking threshold decay is not exponential despite fitting one approximately. — ch. 8
  118. Auditory threshold for broadband noise is set by the most sensitive frequency region only — ch. 8
  119. Postmasking stays at simultaneous-masking level for 5ms then decays to quiet by 200ms. — ch. 8
  120. Low-frequency maskers mask most during their rarefaction phase — ch. 8
  121. A masker can mask sounds occurring before it is switched on. — ch. 8
  122. Masking-period patterns require masker masking and test bursts under an eighth of the period — ch. 8
  123. Temporal masking patterns comprise simultaneous, post, and premasking effects — ch. 8
  124. Internal nonlinear distortion products, not poorer frequency selectivity, explain noise maskers’ extra low-frequency masking — ch. 8
  125. Psychoacoustical tuning curves grow more asymmetric at higher test-tone levels — ch. 8
  126. Masking-period patterns reveal how masker phase within its period affects audibility — ch. 8
  127. Aperiodic noise maskers are studied using repeated random pulse sequences with long periods. — ch. 8
  128. Very brief test tones stay within a critical band only at high centre frequencies. — ch. 8
  129. Masked thresholds spike within milliseconds of masker onset before settling — ch. 8
  130. Broadband maskers overshoot-effect short tones but narrowband maskers do not — ch. 8
  131. Short masker gaps are bridged by postmasking effects — ch. 8
  132. Post masking outlasts premasking and asymmetrically distorts threshold patterns. — ch. 8
  133. Test bursts stay within an eighth of the low-frequency masker’s period — ch. 8
  134. Plosive consonants get masked by preceding loud vowels even in free field — ch. 8
  135. Masking occurs before, during, and after a masker is present. — ch. 8
  136. Noise-burst masked thresholds rise more gradually than tone-burst thresholds with shorter duration — ch. 8
  137. Strong condensation can suppress masking below the quiet threshold — ch. 8
  138. Premasking measurements are only reproducible with trained subjects and remain noisy — ch. 8
  139. Asymmetric pre- and post-masking durations distort symmetric reversals in FM masking patterns. — ch. 8
  140. Frequency-modulated maskers produce two masking peaks where instantaneous frequency crosses the test tone twice — ch. 8
  141. Repeated short tones reach steady threshold when repetition rate exceeds 5 per second — ch. 8
  142. Temporal masking alone masks brief consonants even without room reverberation. — ch. 8
  143. Reducing audible fluctuations in a masker lowers post-masked thresholds by up to 24 dB — ch. 8
  144. Postmasking depends strongly on masker duration and is highly nonlinear. — ch. 8
  145. Envelope-structured sounds produce time-variant temporal masking patterns. — ch. 8
  146. Post masking outlasts premasking and can skew frequency-modulation measurements by nearly 20 dB. — ch. 8
  147. The ear follows frequency-modulated masker dynamics only up to about 8 Hz modulation — ch. 8
  148. Postmasking decay needs two separate time constants depending on masker duration — ch. 8
  149. Shorter masker and test-tone durations flatten the lower slope of pulsation patterns — ch. 9
  150. Positive second derivative of masker drives low-frequency masking-period patterns — ch. 9
  151. Pulsation patterns map test-tone level against frequency like masking patterns do — ch. 9
  152. A gated tone sounds continuous at a level called the pulsation threshold — ch. 9
  153. Pulsation patterns can replicate masking patterns to under 1 dB accuracy — ch. 9
  154. Alternately presented sounds can be perceived as continuous when actually gated — ch. 9
  155. Masking depends on the masker’s acceleration, not its amplitude. — ch. 9
  156. Rarefaction, not masker level, drives the audibility threshold maximum — ch. 9
  157. Simulated Gaussian noise with too few components gives atypical masking results — ch. 11
  158. Intensity-duration tradeoff in masking holds only for durations under 200 ms — ch. 11
  159. Nonsimultaneous masking summation resists simple generalizations — ch. 11
  160. Masking reduces to a comparison of excitation-level patterns over frequency and time — ch. 11
  161. Two simultaneous maskers partition the spectrum where each dominates — ch. 11
  162. Near threshold, masked threshold depends on both masker level and threshold-in-quiet via internal noise — ch. 11
  163. Adding multiple maskers raises masked thresholds most when each contributes equally — ch. 11
  164. Adding two post-maskers together can reduce rather than increase masking — ch. 11
  165. Masking increments peak when the two individual maskers yield equal threshold shifts — ch. 11
  166. Pairs of incoherent or coherent noises can be modeled as amplitude modulation — ch. 11
  167. Combined maskers interact predictably in simultaneous but not nonsimultaneous masking — ch. 11
  168. Post-masking depends on masker bandwidth as well as duration — ch. 11
  169. The minimum masker excitation within its modulation cycle sets masked threshold — ch. 11
  170. Pure-tone versus noise masking differences depend on masker frequency — ch. 11
  171. A frequency-modulated masker’s excursion along the critical-band scale sets the test-tone threshold. — ch. 11
  172. Masking relates closely to excitation level patterns. — ch. 11
  173. Postmasking temporal decay is realizable by a two-resistor two-capacitor diode network — ch. 11
  174. Critical bandwidth varies a hundredfold across the audible range. — ch. 11
  175. Combined masking adds most when the two maskers are equally strong — ch. 11
  176. Simultaneous masking originates in the cochlea while nonsimultaneous masking does not — ch. 11
  177. Post-masking decreases when a second masker suppresses audible masker fluctuations — ch. 11
  178. Masking-induced pitch shift is a product of three pattern-derived factors — ch. 12
  179. Amplitude-modulated broadband noise yields only faint pitch despite flat spectrum — ch. 12
  180. Bandpass noise pitch corresponds to spectral edge frequencies which fuse when close — ch. 12
  181. A spectral gap in switched-off noise yields a tonal afterimage, not a noisy one — ch. 12
  182. Low-pass noise can mask harmonics to create the same virtual-pitch stimulus as filtering. — ch. 12
  183. Most everyday sounds are harmonic complex tones, not pure tones — ch. 12
  184. The spectral pitch model was tuned by fitting published experimental data — ch. 12
  185. Complex-tone pitch tracks the spectral pitch of lower components — ch. 12
  186. Spectral pitch model corrections are segmented into adjustable level ranges — ch. 12
  187. Removing lower harmonics barely changes the perceived pitch of a complex tone. — ch. 12
  188. Maskers below a tone raise its pitch while maskers above lower it. — ch. 12
  189. Medium-level band-stop noise around 43 dB most reliably produces Zwicker tones — ch. 12
  190. Ratio pitch curve shape matches other psychoacoustic frequency-dependence curves — ch. 12
  191. Rippled noise generated by feedback delay produces distinct pitch sensations. — ch. 12
  192. Steep-filtered noise produces pitch matching the filter’s cut-off frequency — ch. 12
  193. Incomplete complex tones show twice the pitch deviation of complete ones — ch. 12
  194. Raising the level of a complex tone shifts its pitch downward. — ch. 12
  195. Narrower noise bands produce single centre pitch rather than edge pitches — ch. 12
  196. Virtual pitch arises only for certain fundamental-to-lowest-component combinations — ch. 12
  197. Pitch of a tone is defined by the matching 40 dB reference frequency — ch. 12
  198. Shifting all spectral components uniformly changes perceived virtual pitch in a sawtooth pattern — ch. 12
  199. Uniformly shifting a harmonic complex tone’s components changes pitch non-monotonically with a sawtooth pattern — ch. 12
  200. Spectral pitch of pure tones derives from three magnitudes of masking patterns — ch. 12
  201. Pure tone pitch shift decomposes additively into level and masking components — ch. 12
  202. Perceived pitch compresses against frequency above roughly 500 Hz — ch. 12
  203. Level-induced pitch shift depends on masking height above the quiet threshold — ch. 12
  204. The gap width producing a Zwicker tone depends on line spacing — ch. 13
  205. Pitch strength is quantifiable by magnitude estimation across diverse sounds — ch. 13
  206. Pitch as a sensory dimension has both height and perceptual strength, which vary independently. — ch. 13
  207. Zwicker-tone pitch sits exactly 1 Bark above the gap’s lower edge — ch. 13
  208. Pitch strength results were normalized per frequency region for comparison across panels. — ch. 13
  209. Higher-frequency gaps need narrower spectral widths to trigger Zwicker tones — ch. 13
  210. Pitch strength rises only modestly with level while loudness explodes. — ch. 15
  211. Pitch strength grows linearly with log duration up to 300 ms. — ch. 15
  212. Steep low-pass noise slopes yield pitch strength far below that of a pure tone — ch. 16
  213. Peaked ripple noise pitch strength stays stable across a wide level range — ch. 16
  214. Narrow spectral bands with steep slopes produce stronger pitch than narrow spectral gaps do — ch. 16
  215. Ripple-noise pitch strength grows linearly with log spectral modulation depth beyond 10 dB — ch. 16
  216. Amplitude discrimination depends on relative loudness increment, not absolute change — ch. 17
  217. A 1 dB level change anchors the model of just-noticeable slow variations. — ch. 17
  218. Auditory critical bandwidth stays constant at 100 Hz below 500 Hz then rises proportionally. — ch. 17
  219. Excitation patterns can be computed from masking data in either direction — ch. 17
  220. Frequency modulation detection is level-independent but thrice frequency-difference detection — ch. 17
  221. Hearing detects AM better than FM only when sidebands fall within a critical bandwidth — ch. 17
  222. Abrupt level changes create audible clicks via broad short-time spectra. — ch. 17
  223. The ear’s upper excitation slope is essential for detecting amplitude modulation at high levels — ch. 17
  224. White noise’s critical-band intensity rises above 5 Bark because bandwidth grows there — ch. 17
  225. Frequency-discrimination and frequency-modulation thresholds are commonly conflated in the literature — ch. 17
  226. Fletcher defined critical bands as noise regions whose power equals a just-masked tone’s — ch. 17
  227. Comparing two tones improves frequency sensitivity beyond detecting a continuous modulation — ch. 17
  228. Low-frequency loudness growth compresses as level rises — ch. 17
  229. Tone-on-tone masking thresholds are measured via narrow-band noise maskers instead — ch. 17
  230. Loudness stays constant below critical bandwidth then grows beyond it — ch. 17
  231. Amplitude-modulated broadband noise yields only 15% of a pure tone’s pitch strength. — ch. 17
  232. Pitch can be modeled as a positional sensation scaled by discrimination steps — ch. 17
  233. The excitation pattern’s upper slope changes nonlinearly with level, unlike the main peak — ch. 17
  234. Just-noticeable level variations always exceed just-noticeable level differences — ch. 17
  235. Raising noise level paradoxically worsens cut-off frequency discrimination as upper slopes flatten. — ch. 17
  236. Amplitude modulation and frequency modulation differ only by sideband phase at low indices — ch. 17
  237. Constant 1-Bark windows yield triangular noise patterns and rectangular tone patterns — ch. 17
  238. Pitch shift magnitude correlates inversely with pitch strength of masked tones — ch. 17
  239. Instrument tuning relies on high harmonics because pitch changes there are easier to hear — ch. 17
  240. Fletcher’s equal-power assumption implies a low-frequency critical band near 50 Hz — ch. 17
  241. Detecting level variation is about 2.5 times harder than detecting level difference — ch. 17
  242. Equal-loudness contours flatten at low frequencies as level rises — ch. 17
  243. Postmasking can last up to 200 milliseconds after a masker ends — ch. 17
  244. Uniform masking noise can substitute for threshold-in-quiet across all frequencies. — ch. 17
  245. Main excitations make critical-band level equal excitation level at signal centers — ch. 17
  246. Hearing becomes less sensitive to frequency variations as level increases — ch. 17
  247. Just-noticeable amplitude modulation of narrow-band noise is near 6 percent at high centre frequencies — ch. 17
  248. A 1 dB level change marks a recurring just-noticeable unit in hearing — ch. 17
  249. Internal physiological noise from blood flow and heartbeat raises low-frequency thresholds — ch. 17
  250. Two-tone maskers define critical bandwidth at the threshold’s transition point. — ch. 17
  251. Changing a tone’s phase alters both its temporal envelope and its instantaneous frequency. — ch. 17
  252. Masked threshold rises once noise bandwidth exceeds the critical bandwidth — ch. 17
  253. White noise shows no sideband-mediated detection ceiling for AM. — ch. 17
  254. Auditory filters respond asymmetrically, favoring frequencies below center — ch. 17
  255. The ear ignores sideband phase once components fall outside one critical band — ch. 17
  256. Amplitude modulation faster than the tone’s own steady pitch is heard as pitch change — ch. 17
  257. Just-noticeable amplitude modulation of noise shrinks from 40% to 6% as bandwidth widens. — ch. 17
  258. Frequency deviation measures one-sided swing while total variation doubles it — ch. 17
  259. Short tone duration inflates JNDF, and level affects low-pass but not high-pass cutoff discrimination. — ch. 17
  260. Binaural envelope-delay sensitivity drops once tone separation exceeds the critical band. — ch. 17
  261. Just-noticeable frequency increments are constant along critical-band rate but rise as pitch strength weakens — ch. 17
  262. Masking shifts detection thresholds and may affect just-noticeable sound changes — ch. 17
  263. Critical bandrate scale stabilizes frequency discrimination measures across durations — ch. 17
  264. Closing the ear canal makes internal body noise audible and measurable — ch. 17
  265. Critical-band rate and excitation level are the intermediate transforms for hearing models — ch. 17
  266. Masked tones recover pitch strength as their level rises above masked threshold — ch. 17
  267. Raising low-pass noise level measurably raises its perceived pitch — ch. 17
  268. A critical band spans roughly 1.3 mm, some 145 hair cells wide. — ch. 17
  269. Pitch from gated noise vanishes when gaps shrink below temporal resolution — ch. 17
  270. Excitation slopes become frequency-independent above 200 Hz center frequency — ch. 17
  271. Loudness measures span quiet, masked, spectral, and temporal domains — ch. 17
  272. Masking shifts thresholds upward and may alter just-noticeable sound changes at all levels. — ch. 17
  273. Narrow-band noise keeps a Gaussian amplitude distribution that statistically modulates its perceived sound — ch. 17
  274. JNDL level dependence unifies across frequency when scaled to loudness level — ch. 17
  275. Maskers’ influence on modulation thresholds vanishes beyond 20 dB above their excitation pattern. — ch. 17
  276. Low-pass noise cutoff discrimination degrades with level while high-pass cutoff does not — ch. 17
  277. Slow amplitude modulation reduces pure tone pitch strength by ten to twenty percent — ch. 17
  278. The phon scale defines loudness relative to equal-loudness matches at 1 kHz — ch. 17
  279. Just-noticeable changes are tenfold worse at masked threshold then normalize 20 dB above — ch. 17
  280. The steep lower slope of the excitation pattern determines frequency modulation detection threshold — ch. 17
  281. Sound direction and field type change perceived loudness at a fixed level. — ch. 17
  282. Level variations within a sound and differences between sounds activate distinct hearing processes. — ch. 17
  283. Phase-change detection yields a critical bandwidth of 150 Hz at 1 kHz — ch. 17
  284. Above a threshold, modulation is heard as separate sideband tones rather than as flutter. — ch. 17
  285. Phase changes become audible in three-tone complexes — ch. 17
  286. Narrow-band noise’s intrinsic amplitude jitter masks external amplitude modulation detection — ch. 17
  287. Barkhausen created the loudness level measure in the 1920s — ch. 17
  288. Band-pass noise audibly self-modulates far above its threshold — ch. 17
  289. Partially masked sounds have a reduced loudness range in both time and spectrum — ch. 17
  290. Rapid AM of noise is heard via overall level, not its rapid fluctuations — ch. 17
  291. Narrow critical bandwidths at low frequencies reduce hearing sensitivity via noise fluctuations — ch. 17
  292. Threshold perception integrates total sound intensity across a limited frequency bandwidth. — ch. 17
  293. Level discrimination for broadband noise is level-independent above 40 dB sound pressure — ch. 17
  294. Frequency discrimination stems from steep filter slopes plus 1 dB level sensitivity — ch. 17
  295. Loudness is measured subjectively against 1 kHz reference tones — ch. 17
  296. Equal-power masking assumption is wrong and only partly power detection holds — ch. 17
  297. Slope excitation can transmit low frequencies to high critical-band regions. — ch. 17
  298. Loudness is the sensation most directly tied to sound intensity — ch. 17
  299. The audible range spans 24 bark-scaled critical bands totaling 0 to 24 Bark. — ch. 17
  300. Shorter tone bursts drastically worsen level discrimination while longer ones do not help — ch. 17
  301. Critical bandwidth at one kilohertz is about 150 hertz — ch. 17
  302. The masking index varies with frequency, distinguishing UEN from uniform masking noise. — ch. 17
  303. Critical bandwidth stays constant with masker level up to about 50 dB. — ch. 17
  304. Frequency discrimination thresholds rise dramatically from 500 Hz to 5000 Hz — ch. 17
  305. Frequency just-noticeable differences rise sharply at low sensation levels — ch. 17
  306. Just-noticeable frequency shifts map to constant basilar distances — ch. 17
  307. Internal bodily noise raises the hearing threshold at low frequencies — ch. 17
  308. Frequency discrimination depends on pitch strength and worsens as pitch strength falls — ch. 17
  309. For broadband noise, AM detection extends up to 500 Hz without sideband interference — ch. 17
  310. Large cutoff-frequency sweeps boost low-pass noise pitch strength 2.4-fold — ch. 17
  311. Noise’s inherent statistical fluctuations degrade frequency-change detectability relative to tones. — ch. 17
  312. Hearing selectivity is modeled via critical-band and excitation intermediate values — ch. 17
  313. At very high modulation rates, listeners detect AM only via average intensity change. — ch. 17
  314. Wider noise bandwidths decrease detectable amplitude modulation via multi-band cooperation — ch. 17
  315. A-weighted dB values misrepresent perceived loudness for complex sounds. — ch. 17
  316. Threshold in quiet depends on total sound intensity within one critical band only — ch. 17
  317. A just-noticeable frequency shift moves basilar excitation a constant 0.05 mm. — ch. 17
  318. Frequency is a poor physical scale for describing inner-ear effects; critical-band rate works better. — ch. 17
  319. Just-noticeable amplitude modulation drops steeply as tone level rises — ch. 17
  320. One just-noticeable pitch step shifts excitation across about six inner hair cells — ch. 17
  321. Critical-band rate correlates with pitch, frequency discrimination, and basilar-membrane position. — ch. 17
  322. Sequential tone comparison yields finer discrimination than modulation detection. — ch. 17
  323. Phase-change sensitivity in hearing is bounded by critical bandwidth, scaling with centre frequency. — ch. 17
  324. Above 500 Hz, Bark scale maps logarithmically to frequency change — ch. 17
  325. Level discrimination thresholds grow steeply near hearing threshold — ch. 17
  326. The basilar membrane yields only about 640 just-noticeable frequency steps end to end. — ch. 17
  327. Overlapping excitation slopes raise the valley minimum by at least 3 dB — ch. 17
  328. Excitation detectors are modeled as independently acting channels with occasional coherence effects — ch. 17
  329. Masking-pattern slope predicts low-pass noise pitch strength better than filter slope does — ch. 17
  330. Adding tones lowers threshold only until about nine tones span the critical band — ch. 17
  331. Temporal partial masking of loudness is robust across sound types and frequencies — ch. 18
  332. Everyday speech communication usually occurs under partial masking conditions — ch. 18
  333. Adjustment methods bias moderate sounds toward louder settings for good audibility. — ch. 18
  334. Loudness perception takes time to develop and so can be interrupted by later sounds — ch. 18
  335. Critical bandwidth at 1 kHz is 160 Hz and governs loudness behavior — ch. 18
  336. Ten-phon increments double loudness, mapping phon to sone by powers of two — ch. 18
  337. Partial masking steepens the loudness function in a way that mirrors hearing recruitment — ch. 18
  338. Medium-separated tones add by intensity once the ear stops tracking envelope — ch. 18
  339. Loudness falls to zero at threshold in quiet, forcing a vertical asymptote — ch. 18
  340. Above 10 Hz, loudness grows 10 phon per tenfold rise in repetition rate. — ch. 18
  341. Total loudness is the integral of specific loudness over critical-band rate — ch. 18
  342. Tone-burst loudness rises 10 phon per tenfold duration up to 100 ms, then plateaus. — ch. 18
  343. Phase differences affect loudness only at low modulation frequencies the ear can track — ch. 18
  344. Uniform exciting noise delivers equal intensity to every critical band — ch. 18
  345. Two tones within a critical band interact to reduce total loudness — ch. 18
  346. Critical bandwidth marks the point where noise loudness begins to grow with bandwidth — ch. 18
  347. Loudness doubles per 10 phon except below 40 phon where it drops steeply. — ch. 18
  348. Widely separated tones add by loudness, not pressure or intensity — ch. 18
  349. A following loud sound reduces the loudness of an earlier short sound — ch. 18
  350. Noise loudness is level-independent until bandwidth exceeds the critical bandwidth. — ch. 18
  351. Steady-state loudness models fail for speech, music, and impulsive technical noises. — ch. 18
  352. Loudness perception shows distinct behavior in two critical-band-defined regions — ch. 18
  353. Narrow-band noise produces substantial loudness in critical-band regions where no physical sound exists — ch. 19
  354. Continuous loudness curves assume the ear has hundreds of movable critical-band filters — ch. 19
  355. Total loudness requires linear scales before integration is valid — ch. 19
  356. Free-field versus diffuse-field transmission gains differ by under eight decibels up to 8 kHz — ch. 19
  357. Wider bandwidth increases perceived loudness at equal sound pressure — ch. 19
  358. Any sound narrower than a critical band produces identical loudness regardless of its width. — ch. 19
  359. Loudness grows as a power law of physical intensity so relative changes match — ch. 19
  360. Threshold in quiet is attributed to internal physiological noise — ch. 19
  361. Specific loudness derives from Stevens’ power law applied to excitation — ch. 19
  362. Spectral summation precedes temporal summation in loudness processing — ch. 19
  363. Specific loudness generalizes beyond loudness to describe sharpness — ch. 19
  364. Uniform exciting noise loudness grows as intensity raised to the 0.23 power — ch. 19
  365. A single exponent of 0.23 governs the loudness power law — ch. 19
  366. Model-computed and measured loudness match across the full level range — ch. 19
  367. Total loudness includes contributions outside the stimulus’s own band — ch. 19
  368. Loudness grows with bandwidth via area tradeoff except at extreme levels — ch. 19
  369. Specific loudness is better expressed against excitation level than against linear excitation — ch. 19
  370. Excitation slopes are steeper toward lower frequencies than higher ones — ch. 19
  371. Loudness rises with bandwidth beyond the critical band despite falling pattern height — ch. 19
  372. The G subscript indicates loudness computed from critical-band levels — ch. 19
  373. Specific loudness rises steeply then saturates toward a power-law asymptote — ch. 19
  374. Threshold in quiet affects loudness mainly for faint sounds — ch. 19
  375. Sharpness changes little with level and bandwidth below one critical band. — ch. 20
  376. Broadband factory noise loudness in phons far exceeds its measured dB level — ch. 20
  377. Adding sound intensities of equal level yields only a three-decibel increase — ch. 20
  378. Spectral envelope, not fine structure, determines perceived sharpness — ch. 20
  379. Loudness processing acts as a temporal low-pass filter with about 45 ms integration time — ch. 20
  380. Loudness patterns approximate specific loudness by ignoring the lower slope entirely. — ch. 20
  381. Timbre is a residual category masking distinct sensations like sharpness and sensory pleasantness. — ch. 20
  382. Third-octave loudness computation requires steady sounds but handles any spectrum — ch. 20
  383. High modulation frequencies increase loudness because spectral spread outweighs temporal fluctuation — ch. 20
  384. ISO 532 B loudness charts span five maximal band levels and two sound-field types — ch. 20
  385. Noise reduction should target the largest loudness pattern area — ch. 20
  386. Vowels dominate perceived loudness while consonants carry intelligibility — ch. 20
  387. Frequency-modulated tones grow louder only above roughly 20 Hz modulation — ch. 20
  388. Timbre served as a residual basket for non-loudness non-pitch sensations — ch. 20
  389. Third-octave band filter leakage flattens the lower slope of measured loudness patterns — ch. 20
  390. Sensory pleasantness decreases as sound sharpness increases — ch. 21
  391. Sensory pleasantness stays flat up to 20 sone then declines with loudness — ch. 21
  392. Narrow-band noise sharpness grows proportionally with critical-band rate up to about 3 kHz — ch. 21
  393. Sensory pleasantness cannot be measured as a single elementary auditory sensation — ch. 21
  394. Noise bandwidth changes sharpness dramatically across a wide range — ch. 21
  395. Fluctuation strength requires at least 3 dB modulation depth before it rises — ch. 21
  396. Loudness reduces sensory pleasantness only beyond roughly 20 sone. — ch. 21
  397. Sharpness is modeled as a weighted first moment of specific loudness — ch. 21
  398. Adding lower-frequency sound can decrease perceived sharpness — ch. 21
  399. A 40-dB level rise increases fluctuation strength by a factor of roughly 2.5 — ch. 21
  400. Sensory pleasantness is computable from sharpness, roughness, tonality, and loudness. — ch. 21
  401. AM noise masking depth is frequency-independent while FM tones are strongly frequency-dependent — ch. 21
  402. Modulation fluctuation strength is governed by excitation patterns — ch. 21
  403. FM-tone fluctuation strength declines with center frequency above 1 kHz while AM does not — ch. 21
  404. Low modulation frequencies produce fluctuation sensation while higher ones produce roughness — ch. 21
  405. The weighted-moment sharpness formula matches measured sharpness across diverse sounds — ch. 21
  406. Listener attitude toward a sound, not just acoustics, shapes perceived pleasantness — ch. 21
  407. Sensory pleasantness rises with tonality only up to a ceiling. — ch. 21
  408. FM fluctuation strength scales with the number of critical bands crossed — ch. 21
  409. The vacil unit anchors fluctuation strength to a 4 Hz modulated tone — ch. 21
  410. Sensory pleasantness depends most on sharpness, then roughness and tonality. — ch. 21
  411. Sensory pleasantness was measured across tones, narrow-band noise, and band-pass noise. — ch. 21
  412. Periodic amplitude fluctuations are perceived as stronger than equivalent random fluctuations. — ch. 21
  413. A closed equation approximates sensory pleasantness from sharpness, roughness, tonality, and loudness — ch. 21
  414. Temporal masking depth is less than envelope modulation depth due to postmasking — ch. 21
  415. Roughness depends on frequency and temporal resolution of hearing — ch. 22
  416. Subjective and physical duration stay proportional only above about 100 ms — ch. 22
  417. A 100 ms tone burst sounds as long as a 400 ms pause does — ch. 22
  418. Roughness depends on modulation degree or FM index plus modulation rate — ch. 22
  419. Subjective duration derives from excitation level, not physical duration — ch. 22
  420. Roughness grows by a factor of three per 40 dB of level increase — ch. 22
  421. Roughness reflects rate of change, so fast modulation roughens while slow change does not — ch. 22
  422. Roughness is limited by frequency selectivity at low and temporal resolution at high frequencies — ch. 22
  423. Plosive pauses of 60-150 ms go unnoticed in speech perception — ch. 22
  424. Roughness only emerges beyond 50 Hz frequency deviation then scales logarithmically — ch. 22
  425. Subjective duration, not physical duration, governs rhythm perception in music — ch. 22
  426. Amplitude-modulated tones produce three distinct sensations depending on modulation frequency — ch. 22
  427. Physically equal spacing only yields subjectively uniform rhythm for steep-envelope bursts — ch. 22
  428. Computer models substitute specific loudness differences where masking-depth data are unavailable — ch. 22
  429. One asper of roughness is standardized by a 70-Hz fully modulated 60-dB tone — ch. 22
  430. Random envelope fluctuations in 100-Hz-wide noise bands produce strong roughness — ch. 22
  431. The perception of uniform rhythm tracks envelope rises, not onsets — ch. 22
  432. Duration perception distortion is largely level-independent above 30 phon — ch. 22
  433. Wideband frequency modulation produces far more roughness than amplitude modulation — ch. 22
  434. Musicians exaggerate physical note and pause durations about fourfold to convey written rhythm — ch. 22
  435. Only about twenty audible roughness steps span the entire perceptual range — ch. 22
  436. Subjective duration of sound bursts can diverge drastically from objective duration — ch. 22
  437. Modulation frequency determines whether sound is heard as fluctuation, roughness, or multiple tones — ch. 22
  438. Perceived duration of pauses differs from perceived duration of equivalent tone bursts — ch. 22
  439. A minority of listeners show quadratic distortion that depends non-ideally on level and phase. — ch. 23
  440. Regular distortion laws from electroacoustics describe hearing’s own nonlinear products — ch. 23
  441. The hearing system becomes less nonlinear at higher input levels. — ch. 23
  442. Cancellation tones alter inner-ear nonlinearity by only 1-2 dB at worst — ch. 23
  443. Quadratic difference tones measured by cancellation originate primarily in the middle ear. — ch. 23
  444. Hearing’s own nonlinearity produces audible difference tones even in distortion-free equipment — ch. 23
  445. Human hearing is most frequency-selective around 2 kHz — ch. 23
  446. Fourth-order distortion products are nearly inaudible and appear only above 85-90 dB. — ch. 23
  447. Cancellation methods quantify the ear’s internally produced difference tones — ch. 23
  448. Rhythm perception can arise from pitch variation alone without loudness change — ch. 23
  449. Hearing-system quadratic distortion is largely independent of frequency separation between primaries. — ch. 23
  450. Quadratic difference tones become audible only above roughly 70 dB primary levels. — ch. 23
  451. Combination tones arise at a place well separated from both primaries. — ch. 24
  452. Large primary frequency separations yield multiple cancellation-level notches — ch. 24
  453. Phase-correct vector summation is essential in cochlear models — ch. 24
  454. Large local excitations can cancel globally because their phases oppose — ch. 24
  455. Individual variability in distortion-product cancellation grows with primary frequency separation — ch. 24
  456. Vector phase differences, not amplitudes, determine cancellation tone levels — ch. 24
  457. Individual differences make averaging meaningless in cancellation-level data — ch. 24
  458. Phase shifts between the ears can substitute for onset time delays in detecting sounds. — ch. 25
  459. Reduced BMLD stems from masking effects, not from signal frequency or masker level — ch. 25
  460. Binaural masking-level difference measures hearing improvement from interaural stimulus asymmetries — ch. 25
  461. Temporal integration up to 200 ms approximates masking for in-band signals — ch. 25
  462. Interaural-delay-tuned channels exist only for frequencies below 1500 Hz — ch. 25
  463. Binaural masking release can be tested under non-simultaneous masking conditions — ch. 25
  464. Interaural phase differences can produce time-delay sensations measured at threshold. — ch. 25
  465. Two ear sounds can differ in phase while differing little in amplitude. — ch. 25
  466. Binaural masking level differences reach 25 dB only for overlapping masker and target — ch. 25
  467. Monotic in-phase masking-level difference is frequency-independent from 250 to 4000 Hz — ch. 25
  468. Binaural hearing enables sound-source direction perception that one ear cannot produce — ch. 25
  469. Ears detect direction changes as small as 5 degrees via 50-microsecond delays — ch. 25
  470. Binaural unmasking depends on masker duration but not signal duration — ch. 25
  471. BMLD magnitude fluctuates wildly with signal timing within a noise burst — ch. 25
  472. Interaural level differences of 1-2 dB produce just-audible lateral displacement — ch. 26
  473. Industry pressure forced ISO to standardize A-weighted SPL before a better loudness-based method — ch. 26
  474. How binaural loudness summation is measured changes the measured effect by several dB — ch. 26
  475. Opposite-phase binaural signals stay louder than in-phase ones up to 40 dB above threshold — ch. 26
  476. Localization precision peaks in front, degrades at the sides, improves behind — ch. 26
  477. Binaural loudness is measured by matching against a monaural comparison tone in filtered noise — ch. 26
  478. Headphone lateralization is one-dimensional whereas free-field localization is three-dimensional for sound images — ch. 26
  479. Out-of-phase binaural tones can double perceived loudness — ch. 26
  480. Interaural level differences and time shifts trade off to cancel each other — ch. 26
  481. Two distinct loudness distributions are used in measurement — ch. 26
  482. Carrier time shifts lateralize only low frequencies; envelope time shifts work at high frequencies — ch. 26
  483. The first arriving sound wave dominates perceived direction of a source — ch. 26
  484. Just-audible image displacement needs only 1 to 2 dB level change. — ch. 26
  485. Computerized loudness models track the 1 kHz tone within 2 percent — ch. 26
  486. Sounds in the median plane are localized to fixed directions based on frequency — ch. 26
  487. Stereo inter-loudspeaker level differences steer perceived sound location between speakers. — ch. 26
  488. Equal-level stereo speakers create a phantom image midway between them — ch. 26
  489. A-weighted SPL was a compromise standard known to give misleading noise results — ch. 26
  490. Lateralization is one-dimensional while localization spans three dimensions — ch. 26
  491. Loudness measures can reveal real improvements A-weighting misses entirely — ch. 27
  492. Annoyance from sounds is quantitatively described as psychoacoustic annoyance. — ch. 27
  493. Inkjet printers are much quieter than needle printers — ch. 27
  494. A-weighting’s underestimate of low-frequency energy explains about four dB of the railway bonus. — ch. 27
  495. A nostalgic ‘Good old Times’ association could explain railway-noise preference — ch. 27
  496. The annoyance formula predicts ratings for real technical sounds. — ch. 27
  497. A-weighted sound power ratios overestimate perceived loudness differences in noise emissions. — ch. 27
  498. Percentile loudness N5 predicts how listeners judge overall noise immission loudness — ch. 27
  499. At equal A-weighted level, railway noise is judged quieter than road and aircraft noise — ch. 27
  500. Perceived loudness of speech matches near-maximum not average loudness — ch. 27
  501. A-weighted sound power exaggerates perceived loudness differences in marketing — ch. 27
  502. Overall noise loudness is judged retrospectively rather than averaged moment to moment — ch. 27
  503. Racing starts and low-gear diesels produce maximal psychoacoustic annoyance — ch. 27
  504. Loudness evaluation may be unchanged by obscuring the sound’s source identity — ch. 27
  505. Speech loudness equals the value exceeded only seven percent of the time — ch. 27
  506. Speech loudness is captured by the 7th-percentile loudness value — ch. 27
  507. The railway bonus persists even when sound sources are obscured, ruling out cognitive effects — ch. 27
  508. Noise reduction claims should use loudness ratios to stay credible — ch. 27
  509. Loudness meter readings predict subjective evaluations better than A-weighted measures — ch. 27
  510. Spectral broadening can mask source identity while preserving loudness-time function — ch. 27
  511. Cognitive source identification can be experimentally decoupled from loudness perception — ch. 27
  512. Typical offices lack the acoustics needed to keep speech private. — ch. 27
  513. A-weighted decibels are a rough practical approximation of perceived loudness — ch. 27
  514. Train loudness depends on length and speed, not just type — ch. 27
  515. Source identification affects annoyance but not loudness perception — ch. 28
  516. Identifying a sound source can shift annoyance independent of loudness — ch. 28
  517. Knowing a sound’s source barely affects how loud we rate it — ch. 28
  518. Absent otoacoustic emissions signal abnormal inner or middle ear function — ch. 28
  519. Speech discrimination requires five distinct auditory features — ch. 28
  520. Nearly all normal-hearing babies produce delayed evoked otoacoustic emissions — ch. 28
  521. Normal-hearing test methods rarely transfer to hearing-impaired listeners — ch. 28
  522. Clinical hearing-loss diagnoses rest on subjective psychoacoustic data because human neurophysiology is rarely available. — ch. 28
  523. Otoacoustic emissions and frequency resolution arise in the inner ear, peripheral to the synapse. — ch. 28
  524. Conductive hearing loss shifts tuning curves upward without degrading frequency resolution. — ch. 29
  525. Tuning curve measurements are plotted on a critical-band-rate scale representing basilar membrane distance — ch. 29
  526. Hearing-impaired listeners vary more than normal hearers in quiet threshold, complicating averaging — ch. 29
  527. A gap-based level-discrimination test detects acoustic neurinoma early — ch. 31
  528. Hearing-impaired listeners fail to gain temporal resolution in background noise — ch. 31
  529. Hearing-impaired specific loudness jumps to near-normal values 20 dB above threshold — ch. 31
  530. Outer hair cell loss alone can account for the recruitment effect — ch. 31
  531. Hearing aids restore loudness sensitivity but cannot restore damaged frequency selectivity. — ch. 31
  532. Impaired frequency selectivity directly causes poor speech discrimination — ch. 31
  533. Noise-induced hearing loss flattens temporal masking valleys and breaks the threshold triad alignment — ch. 31
  534. Recruitment can explain why loudness summation is absent in noise-induced hearing loss — ch. 31
  535. Temporal resolution is quantified by peak and valley masker thresholds — ch. 31
  536. In hearing-impaired regions loudness grows far faster with level — ch. 31
  537. Acoustic neurinoma distinctly elevates level-difference thresholds while most hearing impairments do not. — ch. 31
  538. Noise-impaired listeners show reduced temporal integration, only 4 dB per decade — ch. 31
  539. Noise-induced high-frequency threshold shifts can make previously inaudible difference tones audible — ch. 31
  540. Outer hair cell damage explains recruitment by disabling active cochlear gain — ch. 31
  541. Recruitment means steep loudness growth that catches up to normal at high levels — ch. 31
  542. Normal listeners show a straight-line relation for the quiet-modulated-continuous threshold triad — ch. 31
  543. Simulated hearing loss via masking preserves temporal integration, unlike real loss — ch. 31
  544. Speech-noise test backgrounds were upgraded to match both spectral and temporal envelopes — ch. 31
  545. Audibility thresholds rise about 10 dB per tenfold sound duration reduction — ch. 31
  546. Temporal masking patterns are characterized by peak and valley values. — ch. 31
  547. Hearing-impaired listeners gain far less from noise gaps than normal listeners — ch. 32
  548. Inhibitory networks that sharpen spectral peaks can aid listeners with reduced frequency selectivity — ch. 32
  549. Auditory Gestalt perception mirrors vision through spectral-pitch contours — ch. 32
  550. Sensory consonance depends on roughness, sharpness, and tonalness — ch. 32
  551. String instruments naturally produce inharmonic partial spectra. — ch. 32
  552. Hearing’s salient spectral features can be matched by adjustable Fourier analysis — ch. 32
  553. Adding noise can make listeners hear nonexistent high-frequency brilliance in music. — ch. 32
  554. Musical consonance comprises harmony and sensory consonance from separate domains — ch. 32
  555. Partial-tone strength thresholds offer graduated levels of audio data reduction — ch. 32
  556. Psychoacoustic findings explain musician preferences for tympani heads — ch. 32
  557. String instrument inharmonicity may be not merely unavoidable but perceptually desirable — ch. 32
  558. Digital transmission makes meaningful reduction of information flow important. — ch. 32
  559. Audio compression exploits masking to discard inaudible signal parts — ch. 32
  560. The human ear remains the best speech recognizer and should anchor machine systems — ch. 32
  561. Adding soft noise makes listeners perceive brilliance that is not actually present — ch. 32
  562. Fluent speech in all languages fluctuates at about four elements per second — ch. 32
  563. Human hearing adapts to speakers and rooms but the mechanism remains unknown — ch. 32
  564. Combined cochlear implant and hearing aid restores sound localization ability. — ch. 32
  565. Long recovery-time automatic gain control can erase trailing consonant sounds — ch. 32
  566. Normal-hearing listeners need 7 dB lower SNR in fluctuating versus continuous noise — ch. 32
  567. Guitar-string inharmonicity creates audible beats on low strings. — ch. 32
  568. Perceived speech rhythm tracks the loudness-time function of the signal — ch. 32
  569. Skin-stimulation devices and cochlear implants both serve as hearing prostheses for deaf people. — ch. 32
  570. No evidence supports preferring 432 Hz piano tuning over 440 Hz — ch. 33
  571. The 432 Hz grand-piano tuning preference claim fails blind testing — ch. 33
  572. Historic recordings made around 432 Hz allow fair preference testing — ch. 33
  573. Room acoustics should incorporate psychoacoustic not merely physical metrics — ch. 33
  574. Reverberation multiplies perceived speech loudness well beyond measured level gains — ch. 33
  575. Echo loudness decays nonlinearly so level peaks misrepresent perceived peaks — ch. 33
  576. Speech intelligibility in rooms can be predicted from fluctuation strength — ch. 33
  577. Pitch strength of pure tones varies with their frequency — ch. 49
  578. Signals identical in loudness and pitch can differ markedly in pitch strength — ch. 49
  579. Brief tone durations severely impair frequency discrimination — ch. 49
  580. Narrow-band noise self-modulates at 0.64 times its bandwidth — ch. 49
  581. Partial masking of a tone by background noise diminishes as tone level rises — ch. 49
  582. Tone bursts are heard as longer than pauses of equal physical length — ch. 49
  583. A fluctuating noise simulating speech features is a standard test stimulus — ch. 49
  584. Narrow-band noise self-modulation masks external amplitude modulation — ch. 49
  585. Only tones exceeding a level-dependent masked threshold are audible in noise — ch. 49
  586. Harmonic versus inharmonic spectra of a note are plainly perceptible to a listener — ch. 49
  587. The continuity illusion works even with complex signals like music — ch. 49
  588. Magnitude estimation with an anchor uses a fixed 70 dB car sound as reference. — ch. 49
  589. Partially masking a tone shifts its perceived pitch upward — ch. 49
  590. Interaural level differences alone can shift the perceived position of a sound source — ch. 49
  591. Humans can typically discriminate level differences of 1 to 2 dB — ch. 49
  592. Low-pass noise is heard at a pitch matching its cut-off frequency — ch. 49
  593. Narrower noise bandwidth raises pitch strength while higher center frequency also raises it — ch. 49
  594. Two physically present tones produce an audible third tone inside the ear — ch. 49
  595. Loudness halves for every tenfold decrease in tone duration below 100 ms — ch. 49
  596. Healthy hearing detects 1 to 2 dB level changes at 60 dB — ch. 49
  597. Cubic difference tones arise inside the ear, not in the equipment — ch. 49
  598. Listeners perceive missing fundamentals from the harmonics that remain — ch. 49
  599. Critical-band noise masking can be approximated by simple tone complexes — ch. 49

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