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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 141 (1981), S. 283-296 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A closed sound field system for independent stimulation of both cricket hearing organs is described. The system was used to measure acoustic parameters of the peripheral auditory system inGryllus campestris and to analyze inhibitory responses of the omega cell, a segmental auditory interneuron in the prothoracic ganglion. 1. Best sound transmission in the tracheal pathway occurs at 5 kHz. Closing of the prothoracic spiracles results in increased sound transmission but does not influence the frequency of best transmission in most animals (Fig. 6 B). Sound transmission is modulated by abdominal contractions associated with the respiratory cycle (Fig. 7). 2. AttenuationΔ and phase shift ϕ in the tracheal pathway have been determined for the frequency range of 2 to 10 kHz in animals with closed spiracles.Δ shows a minimum at 5 kHz and ϕ increases almost linearly with frequency (Fig. 11). 3. Sound components acting on each side of the large tympanal membrane form a resultant sound pressure based on linear superposition. This resultant sound pressure represents the effective stimulus of the auditory sense organ (Fig. 12). 4. The response of the omega cell is dependent upon both intensity and relative phase of sound signals applied to the tympanal membranes (Fig. 10). 5. At 5 kHz, the response of the omega cell decreases linearly with increasing contralateral (inhibitory) stimulus intensity over a wide range of intensities. The latency between stimulus onset and response is nearly independent of contralateral inhibition (Figs. 15 and 16). 6. Response (spike number) differences between an omega cell and its complementary mirror image cell due to different stimulus intensities at both ears are enhanced by the neuronal mechanism of contralateral inhibition. In one animal the gain in spike number difference at 5 kHz was calculated to be 60% relative to the response difference when contralateral inhibition was disabled. 7. Evidence for a low frequency (f≦2 kHz) ipsilateral inhibition of the omega cell is presented (Fig. 17).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 151 (1983), S. 397-400 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Sound guided through the tracheal tube to the internal tracheal spaces in the region of the cricket ear is capable of eliciting auditory neural responses in the prothoracic ganglion if the tympanal membrane is allowed to vibrate freely. If the tympanal membrane motion is prevented mechanically neural responses are abolished (Fig. 3) whereas the sound pressure in the tracheal air spaces behind the tympanum is increased. 2. If the motion of the tympanum, as measured with laser vibrometry, is prevented by adjusting the internal and external sound pressure, then neural responses cease simultaneously (Fig. 5). 3. These findings demonstrate that motion of the large tympanum is a necessary requisite in the sound transduction process of the cricket ear.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 167 (1990), S. 193-200 
    ISSN: 1432-1351
    Keywords: Receptor ; Hair sensilla ; Air particle movement
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. Filiform hairs of various lengths on the cerci of adult crickets vibrate in a sound field. These movements were measured with a photodetector for sound frequencies from 10 Hz to 200 Hz in the species Acheta domestica, Gryllus bimaculatus and Phaeophilacris spectrum. 2. With low air-particle velocities, the hair shafts were deflected sinusoidally from their resting position, without bending or secondary oscillations (Figs. 2 A, 3 A). At higher velocities (from ca. 80 mm/s peak velocity, depending on the properties of the individual hairs), the shaft struck the cuticular rim of the socket in which the base of the hair is seated (Fig. 2B). This contact was made at an average angular displacement from the resting position of 5.16°±1.0°. 3. The best frequencies of the hairs were found to be between 40 Hz and 100 Hz (Fig. 5A). The slope of the amplitude curve for constant peak air-particle velocity at frequencies below the best frequencies was between 0 and 6 dB/octave. Long hairs had smaller slope values than short hairs (Fig. 5C). 4. At its best frequency the ratio of maximal tip displacement of a hair to the displacement of the air particles in the sound field was between 0.2 and 2. Only a small number of hairs (2 out of 36) showed tip displacements exceeding twice the air-particle displacement. The values of maximal angular displacement were not correlated to hair length (Fig. 5 B). 5. The angular displacement of the hairs was phase shifted with respect to the air-particle velocity by 0° to +45° (phase lead) at sound frequencies around 10 Hz and by -45° to -120° (phase lag) at 200 Hz (Figs. 3C, 4B). At a particular frequency long hairs tended to have larger phase lags than shorter hairs (Fig. 5D).
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 162 (1988), S. 213-223 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Details in the stridulatory movement ofGryllus campestris were investigated using an improved high resolution miniature angle measurement system. The following results were obtained: During the closing (sound producing) stroke, the speed of the plectrum always has the same value (within measuring accuracy) at a given position. Plectrum speed is directly proportional to tooth spacing, which is known to vary along the file. The only exception to this rule were occasions when closing velocities of precisely 2 times the standard value were found. In between values were never recorded. While temperature has a large effect on the opening speed and duration, the closing speed has a very smallQ 10 (0.07) which is equal to theQ 10 of the resonance frequency of the harp. When the harps are removed, the proportionality between tooth spacing and scraper velocity is lost; the velocity is much increased (up to 3-fold) and the variance of the speed is enhanced 5-fold. These results are discussed with respect to 3 hypothetical models explaining the function of the sound generator system. The model describing the cricket sound generator as a clockwork with an escapement system is capable of accommodating all experimental data without any extra assumptions.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary InGryllus bimaculatus females one foreleg was amputated at the coxa-trochanter joint in the 2nd, 4th or 8th/9th larval instar. A leg of up to normal length is regenerated (Fig. 1) but it lacks a functional ear. In spite of the, usually shorter, regenerated foreleg, the adult one-eared crickets show no impairments in walking when tested on a locomotion compensator. Without sound they walk erratically and most of them weakly circle towards the intact side (Fig. 2). With calling song presentation three response types can be distinguished:tracking (Fig. 3A), ‘hanging on’ (Fig. 3B) or continuouscircling towards the intact side (Fig. 3C, D). Turning tendencies in monaurals increase with song intensity and exceed those of intact and bilaterally operated animals (Fig. 4). Course deviations towards the intact side also slightly increase with intensity (Fig. 5). Course stability is reduced compared to that of intact animals but exceeds that of bilaterally operated crickets (Figs. 5, 6). It is best at 60 dB and deteriorates at higher sound intensities (Fig. 6). The percentage of monaurals tracking or ‘hanging on’ decreases with increasing intensity (Fig. 7B). Tracking is established in most animals but it is limited to a narrow intensity range (Fig. 7A, C). Apart from an increased percentage of tracking after early operations (Fig. 7D), there are no prominent changes in orientational parameters with the date of foreleg amputation. Reamputation of the regenerated leg in the adult monaurals does not significantly impair acoustic orientation (Figs. 8, 9), but occlusion of the ipsilateral prothoracic spiracle does (Figs. 10, 11). An attempt is made to correlate the behavioral performance with the activity of auditory interneurons which have undergone morphological and physiological changes (Fig. 12).
    Type of Medium: Electronic Resource
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