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A digital sound editor.

A series of digital computer programs which facilitate the production and control of acoustic stimuli for hearing assessment and research are described. The package, which is available for PDP 11 computers under RT-11, allows sounds to be digitized, adjusted for amplitude and/or dc offset, edited while in digital form, and output to file or tape. The waveform editor package includes facilities to edit sounds in time--with some sections removed or added with temporal precision of 0.1 msec or better. Two or more sounds may also be combined for stereo or monaural (sound-on-sound) output, or two may be concatenated. Together, the programs permit a wide range of manipulations useful in preparing sound stimuli for use in hearing experiments or in clinical audiometry.

Computers↗

A quick test for sound discrimination ability of rats in a single session after preparatory training.

We developed a sound discrimination test combined with a preparatory training procedure. After water deprivation of 48 h, rats were trained to respond to a sound with pedal-pressing to receive a reward of water. Six of the eight trained rats showed pedal-pressing responses to the sound within 4 h of training, and these six were exposed to two different sounds, response to only one of which was rewarded with water. In a single session of 10 h, the rate and latency of pedal-pressing in response to the two sound stimuli were continuously monitored. All six tested rats showed behavioral discrimination between the rewarded and unrewarded sounds within 6 h.

Acoustic Stimulation↗

The discrimination of and orienting to speech and non-speech sounds in children with autism.

The present study aimed to find out how different stages of cortical auditory processing (sound encoding, discrimination, and orienting) are affected in children with autism. To this end, auditory event-related potentials (ERP) were studied in 15 children with autism and their controls. Their responses were recorded for pitch, duration, and vowel changes in speech stimuli, and for corresponding changes in the non-speech counterparts of the stimuli, while the children watched silent videos and ignored the stimuli. The responses to sound repetition were diminished in amplitude in the children with autism, reflecting impaired sound encoding. The mismatch negativity (MMN), an ERP indexing sound discrimination, was enhanced in the children with autism as far as pitch changes were concerned. This is consistent with earlier studies reporting auditory hypersensitivity and good pitch-processing abilities, as well as with theories proposing enhanced perception of local stimulus features in individuals with autism. The discrimination of duration changes was impaired in these children, however. Finally, involuntary orienting to sound changes, as reflected by the P3a ERP, was more impaired for speech than non-speech sounds in the children with autism, suggesting deficits particularly in social orienting. This has been proposed to be one of the earliest symptoms to emerge, with pervasive effects on later development.

Acoustic Stimulation↗

Modulation of early auditory processing by visually based sound prediction.

Brain activity was measured by magnetoencephalography (MEG) to investigate whether the early auditory system can detect changes in audio-visual patterns when the visual part is presented earlier. We hypothesized that a template underlying the mismatch field (MMF) phenomenon, which is usually formed by past sound regularities, is also used in visually based sound prediction. Activity similar to the MMF may be elicited by comparing an incoming sound with the template. The stimulus was modeled after a keyboard: an animation in which one of two keys was depressed was accompanied by either a lower or higher tone. Congruent audio-visual pairs were designed to be frequent and incongruent pairs to be infrequent. Subjects were instructed to predict an incoming sound based on key movement in two sets of trials (prediction condition), whereas they were instructed not to do so in the other two sets (non-prediction condition). For each condition, the movement took 50 ms in one set (Delta = 50 ms) and 300 ms in the other (Delta = 300 ms) to reach the bottom, at which time a tone was delivered. As a result, only under the prediction condition with Delta = 300 ms was additional activity for incongruent pairs observed bilaterally in the supratemporal area within 100-200 ms of the auditory stimulus onset; this activity had spatio-temporal properties similar to those of MMF. We concluded that a template is created by the visually based sound prediction only after the visual discriminative and sound prediction processes have already been performed.

Acoustic Stimulation↗

Scanning silence: mental imagery of complex sounds.

In this functional magnetic resonance imaging (fMRI) study, we investigated the neural basis of mental auditory imagery of familiar complex sounds that did not contain language or music. In the first condition (perception), the subjects watched familiar scenes and listened to the corresponding sounds that were presented simultaneously. In the second condition (imagery), the same scenes were presented silently and the subjects had to mentally imagine the appropriate sounds. During the third condition (control), the participants watched a scrambled version of the scenes without sound. To overcome the disadvantages of the stray acoustic scanner noise in auditory fMRI experiments, we applied sparse temporal sampling technique with five functional clusters that were acquired at the end of each movie presentation. Compared to the control condition, we found bilateral activations in the primary and secondary auditory cortices (including Heschl's gyrus and planum temporale) during perception of complex sounds. In contrast, the imagery condition elicited bilateral hemodynamic responses only in the secondary auditory cortex (including the planum temporale). No significant activity was observed in the primary auditory cortex. The results show that imagery and perception of complex sounds that do not contain language or music rely on overlapping neural correlates of the secondary but not primary auditory cortex.

Acoustic Stimulation↗

Integration of letters and speech sounds in the human brain.

Most people acquire literacy skills with remarkable ease, even though the human brain is not evolutionarily adapted to this relatively new cultural phenomenon. Associations between letters and speech sounds form the basis of reading in alphabetic scripts. We investigated the functional neuroanatomy of the integration of letters and speech sounds using functional magnetic resonance imaging (fMRI). Letters and speech sounds were presented unimodally and bimodally in congruent or incongruent combinations. Analysis of single-subject data and group data aligned on the basis of individual cortical anatomy revealed that letters and speech sounds are integrated in heteromodal superior temporal cortex. Interestingly, responses to speech sounds in a modality-specific region of the early auditory cortex were modified by simultaneously presented letters. These results suggest that efficient processing of culturally defined associations between letters and speech sounds relies on neural mechanisms similar to those naturally evolved for integrating audiovisual speech.

Adult↗

"Semantic" and "acoustic" errors of aphasic and schizophrenic patients in a sound-picture matching task.

Broca's aphasics, Wernicke's aphasics, brain-damaged patients without aphasia, and chronic schizophrenics were tested on a task to match meaningful sounds to one of four pictures. One of the depicted objects was the natural source of the sound, one was an object belonging to the same semantic category as the correct object, one was an object producing acoustically similar sounds as the correct object, and one was an object not related either semantically or acoustically to the correct object. In one item set the "semantic" distractors produced a sound completely different from the presented one; in another item set the "semantic" distractors made practically no specific sounds at all. Broca's and Wernicke's aphasics were shown to have significantly higher total error scores than brain-damaged patients without aphasia and to make significantly more "semantic" errors only on the first item set and "acoustic" errors on both item sets than the brain-damaged patients without aphasia. However, after correcting for guessing the differences between groups with respect to "semantic" and "acoustic" errors vanished. The aphasics' difficulties in coping with the sound-picture matching task might be difficulties in processing the acoustic dimensions of the items. It is, however, suggested that the impairment is not perceptual but of the cognitive kind repeatedly demonstrated in tasks which require the analytic extraction of features of the stimulus or of the concept represented by the stimulus.

Aphasia↗

The effect of refraction and assumed speeds of sound in tissue and blood on Doppler ultrasound blood velocity measurements.

The combined effect of three assumptions relating to refraction, the speed of sound in tissue and the speed of sound in blood on the accuracy of Doppler ultrasound blood velocity measurements has been investigated. A theoretical relationship giving the net velocity measurement error introduced by these three assumptions has derived using a model in which tissue and blood layers are separated by straight, parallel boundaries. This net error is dependent on the assumed and actual speed of sound in tissue, the assumed speed of sound in blood and the Doppler angle, but is effectively independent of the actual speed of sound in blood. For clinical blood velocity measurements, the net error is estimated to be as much as an 8% overestimation of the actual velocity, higher than previously predicted for any of the factors individually. The relationship also predicts a net velocity measurement error in experimental flow systems and string phantoms which is dependent on the speed of sound in the liquid bath. A water bath at room temperature will give an overestimation of approximately 2%. Experimental investigations using conventional and modified string phantoms and a 5-MHz linear phased array system support these conclusions. The effect of perturbing the layers from their parallel orientation has also been considered theoretically and has provided additional support for the above conclusions. These results may help more accurate Doppler velocity measurements in both experimental and clinical settings.

Blood↗

Auditory agnosia restricted to environmental sounds following cortical deafness and generalized auditory agnosia.

We encountered a case of auditory agnosia restricted to environmental sounds, which was associated with the development of bilateral subcortical lesions after suffering a bilateral putaminal hemorrhage. The patient had a history of a putaminal hemorrhage on her left side without any major disability. Three years later, she suffered a putaminal hemorrhage on the other side. The clinical picture started with cortical deafness, then changed to generalized auditory agnosia for verbal and environmental sounds, and finally developed into auditory agnosia confined to the perception of environmental sounds. Her errors in a test of sound recognition were discriminative rather than associative in nature. Neuro-radiological examinations revealed bilateral subcortical lesions involving the fibers from the medial geniculate body to the temporal lobes after bilateral putaminal hemorrhage. This case suggested that the subcortical lesion involving bilateral acoustic radiation could cause either cortical deafness, auditory agnosia of all sounds, or auditory agnosia restricted to environmental sounds.

Agnosia↗

Long-lasting memory of sounds combined with reward in rats.

We investigated the effects of sound stimuli combined with reward on the subsequent sound discrimination. Water-deprived rats were exposed to one of two sounds (S+ or S-) in a trial, and licking a spout only during the presentation of S+ was rewarded with water. The percentage of trials in which licking occurred was calculated separately for S+ and S-, and sound discrimination was estimated from the difference in the percentage. S+ and S- were significantly discriminated during an 8 h period. In the second test after 1-2 weeks, sound discrimination for the same S+ and S- was significantly better than that for the S+ of the previous S- and S- of the previous S+. These findings indicate that the memory of the sounds combined with reward in the first test was maintained for 1-2 weeks.

Acoustic Stimulation↗

Passive sound-localization ability of the big brown bat (Eptesicus fuscus).

The passive sound-localization ability (i.e. minimum audible angle) of the big brown bat, Eptesicus fuscus, was determined using a conditioned avoidance procedure in which the animals were trained to discriminate left sounds from right sounds. The mean threshold of three bats for a 100-ms broadband noise burst was 14 degrees, a value that is about average for mammals. A similar threshold of 15 degrees was obtained for one animal when it was retested with one of its own recorded echolocation calls as the stimulus. The two bats tested on pure-tone localization were able to localize high-frequency, but not low-frequency tones, even when a low-frequency tone was amplitude modulated, a result indicating that these bats are not able to use binaural time-difference cues for localization. Finally, given the width of the bat's field of best vision, as determined by a count of its ganglion-cell density, its sound-localization acuity is consistent with the hypothesis that the role of passive sound localization is to direct the eyes to the source of a sound.

Acoustic Stimulation↗

Simultaneously active pre-attentive representations of local and global rules for sound sequences in the human brain.

Regular sequences of sounds (i.e., non-random) can usually be described by several, equally valid rules. Rules allowing extrapolation from one sound to the next are termed local rules, those that define relations between temporally non-adjacent sounds are termed global rules. The aim of the present study was to determine whether both local and global rules can be simultaneously extracted from a sound sequence even when attention is directed away from the auditory stimuli. The pre-attentive representation of a sequence of two alternating tones (differing only in frequency) was investigated using the mismatch negativity (MMN) auditory event-related potential. Both local- and global-rule violations of tone alternation elicited the MMN component while subjects ignored the auditory stimuli. This finding suggests that (a) pre-attentive auditory processes can extract both local and global rules from sound sequences, and (b) that several regularity representations of a sound sequence are simultaneously maintained during the pre-attentive phase of auditory stimulus processing.

Acoustic Stimulation↗

The internal auditory clock: what can evoked potentials reveal about the analysis of temporal sound patterns, and abnormal states of consciousness?

Whereas in vision a large amount of information may in theory be extracted from instantaneous images, sound exists only in its temporal extent, and most of its information is contained in the pattern of changes over time. The "echoic memory" is a pre-attentive auditory sensory store in which sounds are apparently retained in full temporal detail for a period of a few seconds. From the long-latency auditory evoked potentials to spectro-temporal modulation of complex harmonic tones, at least two automatic sound analysis processes can be identified whose time constants suggest participation of the echoic memory. When a steady tone changes its pitch or timbre, "change-type" CP1, CN1 and CP2 potentials are maximally recorded near the vertex. These potentials appear to reflect a process concerned with the distribution of sound energy across the frequency spectrum. When, on the other hand, changes occur in the temporal pattern of tones (in which individual pitch changes are occurring at a rate sufficiently rapid for the C-potentials to be refractory), a large mismatch negativity (or MN1) and following positivity (MP2) are generated. The amplitude of these potentials is influenced by the degree of regularity of the pattern, larger responses being generated to a "deviant" tone when the pitch and time of occurrence of the "standards" are fully specified by the preceding pattern. At the sudden cessation of changes, on resumption of a steady pitch, a mismatch response is generated whose latency is determined with high precision (in the order of a few milliseconds) by the anticipated time of the next change, which did not in fact occur. The mismatch process, therefore, functions as spectro-temporal auditory pattern analyser, whose consequences are manifested each time the pattern changes. Since calibration of the passage of time is essential for all conscious and subconscious behaviour, is it possible that some states of unconsciousness may be directly due to disruption of internal "clocks"? Abnormal mismatch potentials may provide a manifestation of a disordered auditory time-sense, sometimes being abolished in comatose patients while the C-potentials and similar responses to the onset of tones are preserved. Both C- and M-potentials were usually found to be preserved, however, in patients who had emerged from coma and were capable of discriminating sounds. Substantially intact responses were also recorded from three patients who were functionally in a "vegetative" state. The C- and M-potentials were once again dissociated in a group of patients with multiple sclerosis, only the mismatch potentials being found to be significantly delayed. This subclinical impairment of a memory-based process responsible for the detection of change in temporal sound patterns may be related to defects in other memory domains such as working memory.

Acoustic Stimulation↗

Sustained blood oxygenation and volume response to repetition rate-modulated sound in human auditory cortex.

The blood oxygen level-dependent (BOLD) signal time course in the auditory cortex is characterized by two components, an initial transient peak and a subsequent sustained plateau with smaller amplitude. Because the T(2)(*) signal detected by functional magnetic resonance imaging (fMRI) depends on at least two counteracting factors, blood oxygenation and volume, we examined whether the reduction in the sustained BOLD signal results from decreased levels of oxygenation or from increased levels of blood volume. We used conventional fMRI to quantify the BOLD signal and fMRI in combination with superparamagnetic contrast agent to quantify blood volume and employed repetition rate-modulated sounds in a silent background to manipulate the response amplitude in the auditory cortex. In the BOLD signal, the initial peak reached 3.3% with pulsed sound and 1.9% with continuous sound, whereas the sustained BOLD signal fell to 2.2% with pulsed sound and to 0.5% with continuous sound, respectively. The repetition rate-dependent reduction in the sustained BOLD amplitude was accompanied by concordant changes in sustained blood volume levels, which, compared to silence, increased by approximately 30% with pulsed and by approximately 10% with continuous sound. Thus, our data suggest that the reduced amplitude of the sustained BOLD signal reflects stimulus-dependent modulation of blood oxygenation rather than blood volume-related effects.

Acoustic Stimulation↗

Suppression of slag foaming by a sound wave.

The aim of this work was to study the effects of sound frequency, sound intensity and viscosity of slag on the slag foaming rate and the steady-state foam height. Experiments were carried out using two slags (BaO-B2O3) melted at a temperature of 1223 or 1273 K, as well as water-glycerin solutions at room temperature. Low frequency sound waves (< 1.3 kHz) are found to be more effective in the slag foaming suppression than high frequency waves (1.3-12 kHz). The steady-state foam height decreases abruptly when the sound pressure reaches a threshold value that depends on sound frequency and liquid viscosity. The results can be explained in terms of enhancing the rates of liquid drainage and film rupture induced by sound.

Journal Article↗

Spectro-temporal analysis of complex tones: two cortical processes dependent on retention of sounds in the long auditory store.

OBJECTIVES: To examine whether two cortical processes concerned with spectro-temporal analysis of complex tones, a 'C-process' generating CN1 and CP2 potentials at cf. 100 and 180 ms after sudden change of pitch or timbre, and an 'M-process' generating MN1 and MP2 potentials of similar latency at the sudden cessation of repeated changes, are dependent on accumulation of a sound image in the long auditory store. METHODS: The durations of steady (440 Hz) and rapidly oscillating (440-494 Hz, 16 changes/s) pitch of a synthesized 'clarinet' tone were reciprocally varied between 0.5 and 4.5 s within a duty cycle of 5 s. Potentials were recorded at the beginning and end of the period of oscillation in 10 non-attending normal subjects. RESULTS: The CN1 at the beginning of pitch oscillation and the MN1 at the end were both strongly influenced by the duration of the immediately preceding stimulus pattern, mean amplitudes being 3-4 times larger after 4.5 s as compared with 0.5 s. CONCLUSIONS: The processes responsible for both CN1 and MN1 are influenced by the duration of the preceding sound pattern over a period comparable to that of the 'echoic memory' or long auditory store. The store therefore appears to occupy a key position in spectro-temporal sound analysis. The C-process is concerned with the spectral structure of complex sounds, and may therefore reflect the 'grouping' of frequency components underlying auditory stream segregation. The M-process (mismatch negativity) is concerned with the temporal sound structure, and may play an important role in the extraction of information from sequential sounds.

Acoustic Stimulation↗

The perception of speech sounds by the human brain as reflected by the mismatch negativity (MMN) and its magnetic equivalent (MMNm).

The present article outlines the contribution of the mismatch negativity (MMN), and its magnetic equivalent MMNm, to our understanding of the perception of speech sounds in the human brain. MMN data indicate that each sound, both speech and nonspeech, develops its neural representation corresponding to the percept of this sound in the neurophysiological substrate of auditory sensory memory. The accuracy of this representation, determining the accuracy of the discrimination between different sounds, can be probed with MMN separately for any auditory feature (e.g., frequency or duration) or stimulus type such as phonemes. Furthermore, MMN data show that the perception of phonemes, and probably also of larger linguistic units (syllables and words), is based on language-specific phonetic traces developed in the posterior part of the left-hemisphere auditory cortex. These traces serve as recognition models for the corresponding speech sounds in listening to speech. MMN studies further suggest that these language-specific traces for the mother tongue develop during the first few months of life. Moreover, MMN can also index the development of such traces for a foreign language learned later in life. MMN data have also revealed the existence of such neuronal populations in the human brain that can encode acoustic invariances specific to each speech sound, which could explain correct speech perception irrespective of the acoustic variation between the different speakers and word context.

Brain↗

Polychlorinated biphenyl concentrations in adult chinook salmon (Oncorhynchus tshawytscha) returning to coastal and Puget Sound hatcheries of Washington State.

Identifying the source of polychlorinated biphenyls (PCBs) is the first step to eliminating contamination within anadromous salmonids and other aquatic species. We evaluated PCB concentrations in the muscle tissue of 4-year old Puget Sound and coastal hatchery Chinook salmon in an effortto identify potential locations where contamination occurs. Ten muscle samples were taken from each of two Puget Sound hatcheries and two coastal hatcheries in Washington State to determine PCB concentrations. Two technical mixtures of PCBs, Aroclor 1254 and Aroclor 1260, were measured in the tissue samples collected. Aroclor 1254 was detected in all samples, while Aroclor 1260 was detected in 16 of 40 samples. Generalized linear modeling (GLM) was used to evaluate the influence of region (Puget Sound and coast), hatchery, sex, fish length, and percent lipids on PCB concentrations. Twenty different GLMs representing multiple null hypotheses were ranked using Akaike Information Criterion (AIC). Six of the 20 models evaluated had substantial support for being the best model to describe PCB concentrations in Chinook salmon. The six models with substantial support were region and lipids; region; hatchery and lipid; region and sex; region, sex, and lipids; and region and length. Region appears to be the most influential variable explaining the variation in PCB concentrations in Chinook salmon in the Pacific Northwest. PCB concentrations in Chinook salmon muscle tissue from Puget Sound hatcheries were significantly greater (mean 49.26 microg/kg wet weight and standard deviation 40.55 microg/kg) than those from coastal hatcheries (mean 17.41 microg/kg wet weight and standard deviation 6.8 microg/kg). Our results suggest that some contamination likely occurs in the Pacific Ocean. However, a larger source likely exists within Puget Sound or along the migratory route of Puget Sound Chinook salmon. The observation of PCBs in Chinook salmon also has important implications for human health and salmon carcass supplementation.

Animals↗