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Query: UNIPROT:P50583 (
asymmetrical
)
12,197
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
1. The maximum acoustic gain of the
external ear
in Macroderma gigas was found to be 25-30 dB between 5-8 kHz and in Nyctophilus gouldi it reached 15-23 dB between 7-22 kHz. Pinna gain reached a peak of 16 dB near 4.5-6 kHz in M. gigas and 12-17 dB between 7-12 kHz in N. gouldi, with average gain of 6-10 dB up to 100 kHz. Pinna gain curves resemble that of a finite conical horn, including resonance. 2. The directional properties of the
external ear
in both species result from sound diffraction at the pinna face, as it approximates a circular aperture. The frequency dependent movement of the acoustic axis in azimuth and elevation is attributed to the
asymmetrical
structure of the pinnae. 3. Evoked potentials and neuronal responses were studied in the inferior colliculus. In M. gigas, the neural audiogram has sensitivity peaks at 10-20 kHz and 35-43 kHz, with extremely low thresholds (-18 dB SPL) in the low frequency region. In N. gouldi, the neural audiogram has sensitivity peaks at 8-14 kHz (lowest threshold 5 dB SPL) and 22-45 kHz. Removal of the contralateral pinna causes a frequency dependent loss in neural threshold sensitivity of up to 10-15 dB in both species. 4. The high frequency peak in the audiogram coincides with the sonar energy band in both species, whereas the low frequency region is used for social communication. Highly sensitive low frequency hearing is discussed in relation to hunting in bats by passive listening.
...
PMID:Acoustical and neural aspects of hearing in the Australian gleaning bats, Macroderma gigas and Nyctophilus gouldi. 337 55
The acoustical properties of the
external ear
of the barn owl (Tyto alba) were studied by measuring sound pressure in the ear canal and outer ear cavity. Under normal conditions, pressure amplification by the
external ear
reaches about 20 dB between 3-9 kHz but decreases sharply above 10 kHz. The acoustic gain curve of the outer ear cavity alone is close to that of a finite-length exponential horn between 1.2-13 kHz with maximum gain reaching 20 dB between 5-9 kHz. Pressure gain by the facial ruff produces a maximum of 12 dB between 5-8 kHz and decreases rapidly above 9 kHz. The directional sensitivity of the
external ear
was obtained from pressure measurements in the ear canal. Directivity of the major lobe is explained, to a first approximation, by the sound diffraction properties of a circular aperture. Aperture size is based on the average radius (30 mm) of the open face of the ruff. Above 5 kHz, the
external ear
becomes highly directional and there is a 26 degree disparity in elevation between the acoustic axis of the left and right ear. In azimuth, directivity patterns are relocated closer to the midline as frequency increases and the acoustic axis moves at a rate of 20 degree/octave between 2-13 kHz. Movement of the axis can be explained, to a first approximation, by the acoustical diffraction properties of an obliquely truncated horn, due to the
asymmetrical
shape of the outer ear cavity. The directional sensitivity of the barn owl ear was studied by recording cochlear microphonic (CM) potentials from the round window membrane. Between 3-9 kHz, CM directivity patterns are clearly different to the directivity patterns of the
external ear
; CM directionality is abruptly lost above 10 kHz. Above 5 kHz, CM directivity patterns are characterized by an elongated major lobe containing the CM axis, forming a tilted band of high amplitude but low directionality (CM axial plane), closely bordered by minima or nulls. The highest directionality is found in the CM directional plane, approximately perpendicular to the CM axial plane. The left and right ear axial planes are symmetrical about the interaural midline (tilted 12 degrees to the right of the midline of the head) and inclined by an average of 60 degrees to the left and right respectively. In azimuth, the CM axis moves towards the midline at a rate of 37 degrees/octave as frequency increases from 2-9 kHz, crossing into contralateral space near 7 kHz.(ABSTRACT TRUNCATED AT 400 WORDS)
...
PMID:Directional hearing in the barn owl (Tyto alba). 338 64
Ear anomalies and hearing loss are major components of CHARGE Syndrome. This paper describes the
external ear
anomalies found in this syndrome: short wide pinnae, often cupped and
asymmetrical
; distinctive triangular concha; discontinuity between the antihelix and antitragus; and 'snipped-off' portions of the helical folds. The patterns of anomalies are so distinctive that a preliminary diagnosis of CHARGE Syndrome can often be made on the basis of ear shape alone. Part II of this communication describes hearing loss in this syndrome.
...
PMID:CHARGE syndrome. Part I. External ear anomalies. 357 Jun 80
We measured the movements of the
external ear
, or pinna, using the magnetic search coil technique in cats trained to look at auditory and visual targets for a food reward. No behavioral contingencies were placed on pinna movements. Prominent pinna movements accompany eye movements when the animal orients to either auditory or visual stimuli. In visual trials the pinna movements are coordinated with eye movements, suggesting that they are part of the general orientation response of the animal. In auditory trials the pinna response was composed of two movements: short- and long-latency components. Whereas the long-latency component seemed to occur with the eye movement to the target, the short-latency component was coupled to the onset of the stimulus. The short-latency component ( approximately 25 msec) was highly
asymmetrical
, being largest in the pinna ipsilateral to the stimuli. In one animal it persisted after >10(5) trials.
...
PMID:Pinna movements of the cat during sound localization. 959 1