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  • Articles: DFG German National Licenses  (3)
  • 1975-1979  (3)
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  • Articles: DFG German National Licenses  (3)
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Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 115 (1977), S. 119-133 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 1. In horseshoe bats temporal response patterns to pure tone stimuli (10–100 kHz, 20 ms duration, 0.5 ms rise/fall-time) of 149 cochlear nucleus units (DCN and PVCN) have been recorded. 2. Distribution of the units' Best Frequencies (BF): low frequency neurons 26% (BF 10–65 kHz); FM-frequency neurons 20% (BF 65–81 kHz, i.e. frequencies occurring in the FM-part of the bat's echo signal); filter frequency neurons 52% (BF 81–88 kHz, i.e. frequencies occurring in the CF-part of the bat's echo signal); high frequency neurons 2% (BF 〉 88 kHz) (Table 1). 3. According to PST-histograms the neurons were classified as: sustained responders (28%, Fig. 1D, E); transient responders (51%, Fig. 1A–C); negative responders (4%, Fig. 1F) and complex responders (17%, Fig. 2–4). In the latter class response patterns drastically change with stimulus frequency and intensity. These units have suppressory sidebands on one or both sides of the excitatory field, sometimes overlapping and enclosing the excitatory area (Fig. 2 and 4). Frequently excitatory response patterns display simultaneous inhibitory processes the latency and duration of which depend on stimulus parameters. 4. In a few complex responders two or more excitatory areas exist, the BF of which may be harmonically related (Fig. 3 and 4). 5. Tuning curves of four auditory nerve fibers are reported showing two separate excitatory areas: a broad less sensitive one from 37 to 79 kHz (low frequency tail) and a narrow, more sensitive one from 82 to 90 kHz (Fig. 5).
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 125 (1978), S. 217-225 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The responses of 230 single neurons in the inferior colliculus of the horseshoebat to single tones have been studied, emphasizing systematic analysis of the effective frequency bands, dynamic properties and the time course of responses. Distribution of the units' best excitatory frequencies (BEF) is: low frequency neurons 23% (BEF 3–65 kHz); FM-frequency neurons 25% (BEF 65–81 kHz, i.e., frequencies occurring in the FM-part of the bat's echo signal); filter neurons 45% (BEF 81–88 kHz, i.e., frequencies occurring in the stabilized CF-part of the bat's echo=reference frequency (RF)); high frequency neurons about 7% (BEF 〉 88 kHz). Tuning curves show conventional shapes (Fig. 1), apart from those of filter neurons, which are extremely narrow. Accordingly, Q10dB-values (BEF divided by the bandwidth of the tuning curve at 10 dB above threshold) are 80–450 in filter neurons (Fig. 2). Response patterns (Fig. 3) are similar to those of Nucleus cochlearis units (transient, sustained, negative and complex responders) with an increased percentage of complex responders up to 38% and a decreased number of transient responders. All types of spike-count functions are found (Fig. 4); nonmonotonic ones dominating. Maximal spike counts are not at the BEF but a few kHz below. Distinct upper thresholds, especially at the BEF of filter neurons (Fig. 5) lead to abrupt changes in activity by slightly shifting stimulus frequency or intensity. The hallmark of inferior colliculus neurons is inhibition, disclosed by distinct inhibitory areas enfolding and overlapping excitatory ones (Figs. 3 and 5). Duration of inhibition varies with stimulus frequency, but is largely independent of stimulus duration (Fig. 6), whereas rebound of inhibition depends on stimulus duration building up periodic rebound activities, if stimulus duration is lengthened. In addition, there are neurons responding only periodically, regardless of stimulus frequency and intensity (Fig. 7). Inhibition is discussed in terms of improving the neuronal signal/spontaneous noise ratio and altering responsiveness of neurons after stimulation, so that these neurons may be suited to time processing in the acoustic pathway.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of comparative physiology 106 (1976), S. 111-125 
    ISSN: 1432-1351
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary For echolocation,Rhinolophus ferrumequinum emits orientation sounds, each of which consists of a long constant-frequency (CF) component and short frequency-modulated (FM) components. The CF component is about 83 kHz and is used for Doppler-shift compensation. In this bat, single auditory nerve fibers and cochlear nuclear neurons tuned at about 83 kHz show low threshold and very sharp filter characteristics. The slopes of their tuning curves ranged between 1,000 and 3,500 dB/octave and their Q-10 dB values were between 20 and 400, 140 on the average (Figs. 3–5). The peripheral auditory system is apparently specialized for the reception and fine frequency analysis of the CF component in orientation sounds and Doppler-shift compensated echoes. This specialization is not due to suppression or inhibition comparable to lateral inhibition, but due to the mechanical specialization of the cochlea. Peripheral auditory neurons with the best frequency between 77 and 87 kHz showed not only on-responses, but also off-responses to tonal stimuli (Figs. 1, 2, and 6). The off-responses with a latency comparable to that of N1-off were not due to a rebound from either suppression or inhibition, but probably due to a mechanical transient occurring in the cochlea at the cessation of a tone burst.
    Type of Medium: Electronic Resource
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